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  1. Uesaka@
  2. 5022@
  3. Trimethylenemethane@
  4. Aldehydes@
  5. Cation
  6. Displaced
  7. Induced@
  8. Transition
  9. 1993@
  10. Alkoxyalkyllithiums@
  11. Backbone@
  12. Clemeolide@
  13. Diastereofacial@
  14. Esters@
  15. Modification@
  16. P-allylnickel
  17. Reagents
  18. Sulfates@
  19. Trimethylaluminum@
  20. HBAM2016AUG95
  21. Pro 3.0
  22. N^ _XON
  23. N^ _XON
  24. gPp??
  25. XOYO K/(
  26. $LRJ/
  27. N^ _O
  28. (@ @ (
  29. $H@B@
  30. $HABA
  31. $H@B@
  32. EMBOg$ 
  33. $HABA
  34. EMBSf
  35. $HABA
  36. $HABA
  37. review
  38. kagan
  39. tetrahedron
  40. generation
  41. iminium
  42. ionization
  43. rearrangem@
  44. duction
  45. dibal
  46. tribal
  47. diisobutylaluminium
  48. hydride
  49. tributyltin@
  50. review
  51. kagan
  52. tetrahedron
  53. aspidosperma
  54. alkaloids
  55. cyclization
  56. secodine
  57. intermedi@
  58. bickelhaupt
  59. friedrich
  60. willen
  61. small
  62. strained
  63. cycl@
  64. bradshaw
  65. izatt
  66. christensen
  67. synthetic
  68. chlorotrimethyl
  69. silyl
  70. accelerated
  71. conjugate
  72. addition
  73. orga@
  74. hodge
  75. sherington
  76. polymer
  77. supported
  78. reactions
  79. n-glycoprotein-proce@
  80. practica
  81. useful
  82. methods
  83. enantioselective
  84. reducti@
  85. synthesis
  86. absolute
  87. configuration
  88. optical
  89. purity
  90. chira@
  91. tandem
  92. fragmentation
  93. cyclopropylcarbinyl
  94. radicals
  95. toyota
  96. yoshifuji
  97. masaaki
  98. extremely
  99. bulky
  100. lithium
  101. trialk@
  102. HBAM3016AUG95@
  103. abalonin
  104. abalonin
  105. abboud
  106. abboud
  107. notario
  108. bertran
  109. abd-el-aziz
  110. abd-el-aziz
  111. abdalla
  112. abdel-magid
  113. abdel-magid
  114. abdellatif
  115. abdellatif
  116. abdelmonem
  117. abdelmonem
  118. abdou
  119. abdreimova
  120. abdreimova
  121. abdulganeva
  122. abdulganeva
  123. erzhanov
  124. abdulla
  125. abdulla
  126. abdulla
  127. brinkmeyer
  128. rohmer
  129. prestwich
  130. abelman
  131. abelman
  132. abramova
  133. abramovitch
  134. abramovitch
  135. abramovitch
  136. barton
  137. finet
  138. abramowicz
  139. abramowicz
  140. abushanab
  141. abushanab
  142. acheson
  143. acheson
  144. achiwa
  145. achiwa
  146. curci
  147. edwards
  148. hadjiarapoglou
  149. richter
  150. waldemar
  151. adams
  152. adams
  153. adams
  154. bhatnagar
  155. adams
  156. adams
  157. spero
  158. adams
  159. adant
  160. adant
  161. addlington
  162. addlington
  163. barrett
  164. adekov
  165. adekov
  166. minkin
  167. adembri
  168. adembri
  169. andersch
  170. berger
  171. goergens
  172. seemayer
  173. schneider
  174. adkins
  175. adkins
  176. adlington
  177. adlington
  178. adlington
  179. adrian
  180. adrian
  181. young
  182. afanasiev
  183. afarinkia
  184. afarinkia
  185. afarinkia
  186. vinader
  187. nelson
  188. posner
  189. agafonov
  190. agami
  191. agami
  192. agemann
  193. agemann
  194. klamann
  195. aggarwal
  196. aggarwal
  197. aggarwal
  198. varinder
  199. kumar
  200. agosta
  201. agreda
  202. agreda
  203. zoeller
  204. agrofoglio
  205. agrofoglio
  206. suhas
  207. farese
  208. condom
  209. challand
  210. aguero
  211. aguero
  212. osborn
  213. aguilar
  214. aguilar
  215. ahlberg
  216. ahlberg
  217. jonsll
  218. engdahl
  219. ahlbrecht
  220. ahlbrecht
  221. ahmad
  222. ahmad
  223. ahman
  224. ahman
  225. ahmed
  226. ahmed
  227. ahuja
  228. ahuja
  229. jaimala
  230. aiello
  231. aitken
  232. aitken
  233. aitken
  234. kilenyi
  235. aizawa
  236. aizawa
  237. aizpurua
  238. aizpurua
  239. akaji
  240. akaji
  241. akazome
  242. akazome
  243. akelah
  244. akelah
  245. akhmetov
  246. akhmetov
  247. karimov
  248. shcherbakova
  249. porshnev
  250. cherk
  251. akhrem
  252. akhtar
  253. akhtar
  254. wright
  255. akira
  256. akiya
  257. akiyama
  258. akiyama
  259. bednarski
  260. simon
  261. waldmann
  262. whiteside
  263. akiyama
  264. akkerman
  265. akse'nov
  266. akse'nov
  267. vlasov
  268. shnitko
  269. akssira
  270. akssira
  271. al-awadi
  272. al-omran
  273. al-saleh
  274. al-talib
  275. al-talib
  276. tashtoush
  277. alabed
  278. alabed
  279. millard
  280. katritzsky
  281. alauddin
  282. alazard
  283. alazard
  284. alber
  285. alber
  286. alberg
  287. albericio
  288. albers
  289. albers
  290. coville
  291. albers
  292. robinson
  293. singleton
  294. albert
  295. albertson
  296. albertson
  297. albini
  298. albini
  299. albini
  300. fasani
  301. mella
  302. albini
  303. mella
  304. freccero
  305. albini
  306. pietra
  307. albini
  308. albini
  309. angelo
  310. albizati
  311. albizati
  312. albrecht
  313. albrecht
  314. erker
  315. kruger
  316. albright
  317. albright
  318. albright
  319. albright
  320. burdett
  321. whangbo
  322. alcaide
  323. alcaide
  324. alcalde
  325. alcalde
  326. alcaraz
  327. alcaraz
  328. alder
  329. alder
  330. aldoshin
  331. aldoshin
  332. aldulayymi
  333. aldulayymi
  334. aldulayyni
  335. aldulayyni
  336. aleksandrov
  337. alekseev
  338. alekseeva
  339. alekseeva
  340. yakhontov
  341. aleshkova
  342. aleshkova
  343. alexakis
  344. alexakis
  345. alexakis
  346. chuit
  347. commercon-bourgain
  348. foulon
  349. jabri
  350. alexakis
  351. commercon
  352. coulentianos
  353. normant
  354. alexakis
  355. mangeney
  356. alexakis
  357. mangeney
  358. ghribi
  359. march
  360. sedrani
  361. alexandrov
  362. alexandrov
  363. alexandrov
  364. tarunin
  365. alfimov
  366. alfred
  367. allaf
  368. allakhverdiev
  369. allen
  370. allen
  371. vaillancourt
  372. albizati
  373. allen
  374. angela
  375. allen
  376. allen
  377. allenmark
  378. allenmark
  379. allentoff
  380. allentoff
  381. aller
  382. aller
  383. allinger
  384. allinger
  385. almena
  386. almena
  387. almena
  388. almerico
  389. alonso
  390. alonso
  391. alpegiani
  392. alpegiani
  393. bedeschi
  394. giudici
  395. perrone
  396. visentin
  397. zarini
  398. alpegiani
  399. bedeschi
  400. perrone
  401. zarini
  402. francheschi
  403. alpegiani
  404. bissolino
  405. borghi
  406. shralel
  407. tonani
  408. perrone
  409. alper
  410. alper
  411. alper
  412. alsters
  413. altel
  414. altel
  415. altona
  416. alvarez
  417. alvarez
  418. joule
  419. alvarez
  420. salas
  421. joule
  422. alvhall
  423. amabilino
  424. amabilino
  425. david
  426. amalia
  427. amarnath
  428. amarnath
  429. broom
  430. amarnath
  431. matlhav
  432. amatore
  433. amatore
  434. amputch
  435. amputch
  436. izatt
  437. bradshaw
  438. izatt
  439. anand
  440. anand
  441. singh
  442. anastasiou
  443. anastasiou
  444. anaya
  445. anaya
  446. andersch
  447. anderson
  448. anderson
  449. anderson
  450. leander
  451. anderson
  452. nderson
  453. sanders
  454. andersson
  455. andersson
  456. anderton
  457. anderton
  458. takayama
  459. andreae
  460. andreae
  461. schmitz
  462. andreev
  463. andreev
  464. kolomiets
  465. andreev
  466. kolomiets
  467. fokin
  468. andrei
  469. andreoli
  470. andreu
  471. andreu
  472. cecilia
  473. andrew
  474. andrews
  475. andrus
  476. andrus
  477. andryukhova
  478. andryukhova
  479. angela
  480. angeles
  481. angeles
  482. angelici
  483. angelo
  484. angelov
  485. angiolini
  486. angle
  487. angle
  488. angoh
  489. angyal
  490. angyal
  491. anklam
  492. anklam
  493. margaretha
  494. annby
  495. annby
  496. karlsson
  497. gronowitz
  498. hallberg
  499. alvhall
  500. svenson
  501. annunziata
  502. annunziata
  503. anthony
  504. antigoni
  505. antonova
  506. antonova
  507. ioganson
  508. aoyagi
  509. aoyagi
  510. aoyama
  511. aoyama
  512. aoyama
  513. apparu
  514. appel
  515. appel
  516. appendino
  517. appendino
  518. apsimon
  519. apsimon
  520. tokumaru
  521. araki
  522. araki
  523. ochoa
  524. aratani
  525. aratani
  526. arbuzov
  527. arbuzov
  528. zobova
  529. archer
  530. archer
  531. arciniec
  532. arciniec
  533. ardill
  534. ardill
  535. arduengo
  536. arduengo
  537. arduengo
  538. stewart
  539. aresta
  540. aresta
  541. argade
  542. argade
  543. arimoto
  544. arimoto
  545. ariyoshi
  546. arjona
  547. arjona
  548. armarego
  549. armarego
  550. armesto
  551. armesto
  552. armesto
  553. armitage
  554. armitage
  555. armitage
  556. armor
  557. armstrong
  558. trong
  559. armstrong
  560. arnason
  561. arnett
  562. arnett
  563. arnett
  564. flowers
  565. arnold
  566. arnold
  567. arnone
  568. arnone
  569. arseniyadis
  570. arseniyadis
  571. arseniyadis
  572. kyler
  573. arshinova
  574. arshinova
  575. artamkina
  576. artamkina
  577. kovalenko
  578. beletskaya
  579. reutov
  580. artis
  581. artis
  582. artley
  583. artley
  584. artur
  585. arvanitis
  586. arzamastsev
  587. arzoumanian
  588. arzoumanian
  589. metzger
  590. asami
  591. asami
  592. masatoshi
  593. asaoka
  594. asaoka
  595. asfari
  596. asfari
  597. weiss
  598. pappalardo
  599. vicens
  600. asfari
  601. weiss
  602. vicens
  603. asfari
  604. zouhair
  605. ashare
  606. ashby
  607. ashby
  608. ashby
  609. oswald
  610. drone
  611. kausch
  612. kroker
  613. ashry
  614. ashton
  615. aslam
  616. asokan
  617. asokan
  618. asselineau
  619. asselineau
  620. astruc
  621. astruc
  622. astruc
  623. hamon
  624. mandon
  625. moulines
  626. atherton
  627. atherton
  628. sheppard
  629. atta-ur-rahman//bash
  630. atta-ur-rahman//bash
  631. attanasi
  632. attanasi
  633. attardo
  634. attwood
  635. attwood
  636. wovkulich
  637. sonnenberger
  638. atwell
  639. atwell
  640. weyenberg
  641. atwood
  642. auberson
  643. auberson
  644. aubert
  645. aubert
  646. audouin
  647. augeri
  648. augeri
  649. augusti
  650. augusti
  651. aulbach
  652. aumann
  653. aumann
  654. auner
  655. auner
  656. ziche
  657. aurell
  658. aurell
  659. auricchio
  660. auricchio
  661. aurich
  662. aurich
  663. aurich
  664. aurich
  665. nielsen
  666. aurrecoechea
  667. aurrecoechea
  668. austin
  669. avalos
  670. avalos
  671. babiano
  672. cintas
  673. jimenez
  674. palacios
  675. averdung
  676. averdung
  677. avetisyan
  678. avotins
  679. avotins
  680. aylwood
  681. aylwood
  682. aznar
  683. azzena
  684. babad
  685. babad
  686. zeiler
  687. babiano
  688. ramana
  689. ramadas
  690. bachi
  691. bachi
  692. bachi
  693. balanov
  694. bar-ner
  695. bosch
  696. denenmark
  697. mizhiritsk
  698. bachmann
  699. bachmann
  700. hoffman
  701. bachmann
  702. struve
  703. bachowska
  704. baciocchi
  705. baciocchi
  706. backvall
  707. backvall
  708. badanyan
  709. badanyan
  710. melikyan
  711. mkrtchyan
  712. bader
  713. badone
  714. badone
  715. badri
  716. baggott
  717. bailey
  718. bailey
  719. bailey
  720. bailey
  721. bailey
  722. patricia
  723. bailey
  724. patricia
  725. bailey
  726. william
  727. baines
  728. baird
  729. baird
  730. baizer
  731. baizer
  732. baizer
  733. petrovich
  734. bakale
  735. bakale
  736. baker
  737. baker
  738. baker
  739. baker
  740. herbert
  741. baker
  742. swain
  743. baker
  744. bakker
  745. bakulev
  746. balaban
  747. balaban
  748. balachandran
  749. balanov
  750. balaram
  751. balaram
  752. balasubramanian
  753. balasubramanian
  754. balasubramanian
  755. balcerzak
  756. balcerzak
  757. balch
  758. balch
  759. baldwin
  760. baldwin
  761. baldwin
  762. balleni
  763. ballester
  764. ballester
  765. ballini
  766. ballini
  767. bally
  768. bally
  769. masamune
  770. balogh
  771. balogh
  772. laszlo
  773. balyeva
  774. bambino
  775. bambino
  776. bambino
  777. bandini
  778. bandyopadhyay
  779. banerjee
  780. banerjee
  781. gonzalez
  782. banerji
  783. banerji
  784. banert
  785. banfi
  786. banfi
  787. guanti
  788. banfi
  789. banister
  790. banister
  791. rawson
  792. banks
  793. banno
  794. banno
  795. banoub
  796. banoub
  797. boullanger
  798. lafont
  799. bansal
  800. bansal
  801. karaghiosoff
  802. schmidpeter
  803. banwell
  804. banwell
  805. bar-ner
  806. baramee
  807. baramee
  808. baran
  809. baranov
  810. baranov
  811. perekalin
  812. baranovskii
  813. baranovskii
  814. litvinovskaya
  815. khripach
  816. baranowski
  817. barbry
  818. barbry
  819. barco
  820. baretti
  821. barillier
  822. barillier
  823. barkhash
  824. barks
  825. barks
  826. barluenga
  827. barluenga
  828. barluenga
  829. aznar
  830. fustero
  831. tomas
  832. barluenga
  833. joglar
  834. gonzalez
  835. fustero
  836. barluenga
  837. palacios
  838. barluenga
  839. tomas
  840. barluenga
  841. barna
  842. barnes
  843. barnes
  844. barney
  845. barney
  846. barnick
  847. barnick
  848. barrau
  849. barrau
  850. barrau
  851. escudie
  852. satge
  853. barrett
  854. barrett
  855. barrett
  856. graboski
  857. barrett
  858. llace
  859. flygare
  860. barrett
  861. sturgess
  862. barros
  863. barros
  864. barry
  865. barry
  866. iii//bates
  867. beavers
  868. camou
  869. gordon
  870. barry
  871. barta
  872. barta
  873. bartl
  874. bartl
  875. bartl
  876. falbe
  877. bartlett
  878. bartlett
  879. bartmann
  880. bartmann
  881. bartoli
  882. barton
  883. barton
  884. barton
  885. barton
  886. doller
  887. barton
  888. hassel
  889. barton
  890. ollis
  891. barton
  892. parekh
  893. barton
  894. derek
  895. bartsch
  896. bartsch
  897. bartsch
  898. zavada
  899. bartulin
  900. bartulin
  901. basavaiah
  902. basavaiah
  903. basavaiah
  904. krishna
  905. baschang
  906. baschang
  907. bassa
  908. bassa
  909. bassani
  910. bassindale
  911. bassindale
  912. bassner
  913. bastos
  914. batcheller
  915. bates
  916. bathini
  917. bathini
  918. batra
  919. batra
  920. batyeva
  921. baudin
  922. baudler
  923. baudler
  924. glinka
  925. bauer
  926. bauer
  927. exner
  928. bauld
  929. bauld
  930. bauld
  931. baumgarten
  932. baumgarten
  933. martin
  934. baumstark
  935. baumstark
  936. bausch
  937. bausch
  938. bauslaugh
  939. bauslaugh
  940. baxter
  941. baxter
  942. bayer
  943. bayer
  944. bayer
  945. bayer
  946. bayer//m
  947. bayle
  948. bayle
  949. reitz
  950. snieckus
  951. zajdel
  952. reitz
  953. beaucage
  954. beaucage
  955. beavers
  956. becher
  957. becher
  958. stidsen
  959. beck-sickinger
  960. becker
  961. becker
  962. becker
  963. beckhaus
  964. beckhaus
  965. beckwith
  966. beckwith
  967. beddoes
  968. beddoes
  969. bedekar
  970. bedekar
  971. bedeschi
  972. bednarski
  973. beena
  974. beerli
  975. beerli
  976. begley
  977. begley
  978. begue
  979. begue
  980. begue
  981. bonnet-delpon
  982. begue
  983. charpentier-morize
  984. behrens
  985. behrens
  986. sharpless
  987. behrman
  988. behrman
  989. beifuss
  990. beifuss
  991. bekkum
  992. belder
  993. belen'kii
  994. belen'kii
  995. beletskaya
  996. beletskaya
  997. belin
  998. cragg
  999. firestone
  1000. bellina
  1001. bellina
  1002. bellur
  1003. bellur
  1004. nanjundiah
  1005. bellus
  1006. bellus
  1007. beloglazkina
  1008. beloglazkina
  1009. elena
  1010. belov
  1011. belov
  1012. belshaw
  1013. belshaw
  1014. meyer
  1015. johnson
  1016. ikeda
  1017. andrus
  1018. beltaief
  1019. beltaief
  1020. belter
  1021. belter
  1022. benati
  1023. benati
  1024. benbow
  1025. benbow
  1026. bencze
  1027. bencze
  1028. benjamin
  1029. benjes
  1030. benjes
  1031. benkeser
  1032. benkeser
  1033. benkovic
  1034. bennasar
  1035. bennasar
  1036. lavil
  1037. alvarez
  1038. bosch
  1039. benneche
  1040. benner
  1041. benner
  1042. glasfeld
  1043. piccirilli
  1044. bennet
  1045. bennetau
  1046. bennetau
  1047. dunogues
  1048. bennett
  1049. bennett
  1050. bennett
  1051. bennett
  1052. schwemlein
  1053. bennett
  1054. bennett
  1055. bentley
  1056. bentley
  1057. bentley
  1058. bercaw
  1059. berezhnaya
  1060. bergamini
  1061. bergamini
  1062. bergatrom
  1063. bergatrom
  1064. rotstein
  1065. norrix
  1066. bergdahl
  1067. bergdahl
  1068. bergenthal
  1069. berger
  1070. berger
  1071. raadt
  1072. griengl
  1073. hayden
  1074. hechtberger
  1075. klempie
  1076. bergh
  1077. bergh
  1078. bergman
  1079. bergman
  1080. pelcman
  1081. bergmann
  1082. bergmann
  1083. ginsburg
  1084. pappo
  1085. berlan
  1086. berlan
  1087. berlin
  1088. berliner
  1089. berliner
  1090. bernardhenriet
  1091. bernardhenriet
  1092. bernardi
  1093. bernardi
  1094. olivucci
  1095. bernasconi
  1096. bernasconi
  1097. berndt
  1098. berndt
  1099. bernhard
  1100. bernhard
  1101. mayer
  1102. bernhard
  1103. witkop
  1104. berrisford
  1105. berrisford
  1106. berson
  1107. berson
  1108. berson
  1109. jerome
  1110. berthiaume
  1111. berti
  1112. berti
  1113. bertran
  1114. bertrand
  1115. bertrand
  1116. bertrand
  1117. wentrup
  1118. bertrand
  1119. bertucci
  1120. bertz
  1121. bertz
  1122. besse
  1123. veschambre
  1124. besson
  1125. besson
  1126. bestmann
  1127. bestmann
  1128. bestmann
  1129. vostrowski
  1130. bestmann
  1131. zimmermann
  1132. bethell
  1133. bethell
  1134. parker
  1135. bethune
  1136. betschinger
  1137. beugelmans
  1138. beugelmans
  1139. bezuidenhoudt
  1140. bezuidenhoudt
  1141. bhatia
  1142. bhatia
  1143. bhatia
  1144. beena
  1145. bhatnagar
  1146. bhatt
  1147. bhatt
  1148. kulkarni
  1149. bhatt
  1150. bhupathy
  1151. bhushan
  1152. bhuvaneswari
  1153. bhuvaneswari
  1154. bianchi
  1155. bianchi
  1156. micheli
  1157. gandolfi
  1158. bianchini
  1159. bianchini
  1160. bickelhaupt
  1161. bickelhaupt
  1162. bickelhaupt
  1163. biehl
  1164. biehl
  1165. khanapure
  1166. biellmann
  1167. biellmann
  1168. ducep
  1169. biermann
  1170. biermann
  1171. biggadike
  1172. bijoy
  1173. bijoy
  1174. bilha
  1175. billera
  1176. billera
  1177. billington
  1178. billington
  1179. billups
  1180. billups
  1181. billups
  1182. ciufolini
  1183. billups
  1184. haley
  1185. birch
  1186. birch
  1187. williamson
  1188. birkett
  1189. birkett
  1190. birkofer
  1191. birkofer
  1192. stuhl
  1193. bishop
  1194. bishop
  1195. bisht
  1196. bissell
  1197. bissell
  1198. richard
  1199. bissolino
  1200. bjorsvik
  1201. bjorsvik
  1202. black
  1203. black
  1204. black
  1205. blackburn
  1206. blackburn
  1207. davies
  1208. sutton
  1209. whittaker
  1210. blackburn
  1211. blackburn
  1212. ashton
  1213. rogers
  1214. taylor
  1215. guranowsk
  1216. blackmond
  1217. blackmond
  1218. blagoev
  1219. ivanov
  1220. blaser
  1221. blaser
  1222. blaser
  1223. blasko
  1224. blasko
  1225. cordell
  1226. blaszczyk
  1227. blatchly
  1228. blatt
  1229. blatt
  1230. blazevic
  1231. blazevic
  1232. kolbah
  1233. belin
  1234. sunjic
  1235. kajfez
  1236. blechert
  1237. blechert
  1238. bleeke
  1239. bleeke
  1240. bleha
  1241. bleriot
  1242. blicke
  1243. blicke
  1244. blizzard
  1245. blizzard
  1246. bloch
  1247. bloch
  1248. block
  1249. block
  1250. block
  1251. aslam
  1252. blomberg
  1253. blomberg
  1254. blomberg
  1255. hartog
  1256. blomberg
  1257. cornelis
  1258. bloom
  1259. bloomfield
  1260. bloomfield
  1261. owsley
  1262. nelke
  1263. bloxham
  1264. bloxham
  1265. blumenkopf
  1266. blumenkopf
  1267. overman
  1268. blunden
  1269. blunden
  1270. cusack
  1271. smith
  1272. blystone
  1273. blystone
  1274. jenkins
  1275. lawrence
  1276. bobbit
  1277. bobbit
  1278. bourque
  1279. bobbitt
  1280. bobbitt
  1281. flores
  1282. bobosik
  1283. bobosik
  1284. bocelli
  1285. bocelli
  1286. boche
  1287. boche
  1288. boche
  1289. walborsky
  1290. bochkov
  1291. bochkov
  1292. zaikov
  1293. afanasiev
  1294. bockman
  1295. boczon
  1296. boczon
  1297. bodanshky
  1298. bodansky
  1299. bodanszky
  1300. bodanszky
  1301. bodanszky
  1302. martinez
  1303. bodepudi
  1304. bodepudi
  1305. bodurow
  1306. boeckel
  1307. boehmer
  1308. boehmer
  1309. boere
  1310. boere
  1311. boese
  1312. boese
  1313. boestern
  1314. bogdanovic
  1315. bogdanovic
  1316. bogdanovic
  1317. losler
  1318. meister
  1319. pauling
  1320. wilke
  1321. bogen
  1322. bogen
  1323. boger
  1324. boger
  1325. boger
  1326. boger
  1327. weinreb
  1328. boger
  1329. boguslavskaya
  1330. boguslavskaya
  1331. kartashov
  1332. chuvatkin
  1333. bohlmann
  1334. bohlmann
  1335. bohme
  1336. bohme
  1337. bohmer
  1338. bohrisch
  1339. bohrisch
  1340. boivin
  1341. boivin
  1342. boivin
  1343. boland
  1344. boland
  1345. froessl
  1346. lorenz
  1347. boldeskul
  1348. boleslawski
  1349. bolestova
  1350. bollini
  1351. bologna
  1352. bolscher
  1353. bolton
  1354. bolton
  1355. bonacic-koutecky
  1356. bonadies
  1357. bonadies
  1358. bonete
  1359. bonete
  1360. bonini
  1361. bonini
  1362. righi
  1363. bonnemann
  1364. grard
  1365. tanaka
  1366. wilke
  1367. bonnet-delpon
  1368. bontagg
  1369. bontagg
  1370. thomas
  1371. bontagg
  1372. thomas
  1373. boone
  1374. boone
  1375. boons
  1376. boons
  1377. boraldi
  1378. boraldi
  1379. barco
  1380. baretti
  1381. bollini
  1382. simoni
  1383. borden
  1384. borden
  1385. borden
  1386. weston
  1387. thatcher
  1388. bordwell
  1389. bordwell
  1390. bordwell
  1391. zhang
  1392. borghi
  1393. borisova
  1394. borner
  1395. borner
  1396. borovkov
  1397. borovkov
  1398. gneeva
  1399. strekova
  1400. filippovich
  1401. borthwick
  1402. borthwick
  1403. biggadike
  1404. bosch
  1405. bosch
  1406. subhas
  1407. bossio
  1408. bossio
  1409. botteghi
  1410. botteghi
  1411. paganelli
  1412. schionato
  1413. marchetti
  1414. boucherle
  1415. boullanger
  1416. bourgin
  1417. bourgin
  1418. bourhis
  1419. bourhis
  1420. bourque
  1421. bouzard
  1422. bowden
  1423. bowden
  1424. bowman
  1425. bowman
  1426. bowser
  1427. bowser
  1428. boyer
  1429. boyer
  1430. robinson
  1431. boyer
  1432. bradley
  1433. bradshaw
  1434. bradshaw
  1435. bradshaw
  1436. krakowiak
  1437. izatt
  1438. bradsher
  1439. brady
  1440. brady
  1441. braga
  1442. braga
  1443. braga
  1444. dyson
  1445. grepioni
  1446. johnson
  1447. branalt
  1448. branalt
  1449. brand
  1450. branda
  1451. branda
  1452. brandes
  1453. brandes
  1454. brandi
  1455. brandi
  1456. cicchi
  1457. pietrusiewicz
  1458. brandi
  1459. cordero
  1460. sarlo
  1461. guhrna
  1462. brandsma
  1463. brandsma
  1464. brandukova
  1465. brandukova
  1466. vygodskii
  1467. vinogradova
  1468. braun
  1469. braun
  1470. jakob
  1471. oliveros
  1472. oller
  1473. nascimento
  1474. braunstein
  1475. braunstein
  1476. nobel
  1477. braverman
  1478. bravo
  1479. bravo
  1480. resnati
  1481. bredas
  1482. bredas
  1483. bregadze
  1484. bregadze
  1485. breitmaier
  1486. breitmaier
  1487. ullrich
  1488. pottlloff
  1489. bohme
  1490. brotian
  1491. brennan
  1492. breslow
  1493. breslow
  1494. chmielewski
  1495. foley
  1496. johnson
  1497. kumabe
  1498. varney
  1499. breteler
  1500. breuer
  1501. breuer
  1502. breutel
  1503. breutel
  1504. brewster
  1505. brewster
  1506. eliel
  1507. brian
  1508. brieger
  1509. brieger
  1510. bennett
  1511. brieger
  1512. nestrick
  1513. brijoux
  1514. brillon
  1515. brillon
  1516. brindaban
  1517. brindle
  1518. bringmann
  1519. bringmann
  1520. bringmann
  1521. walter
  1522. weirich
  1523. brinker
  1524. brinker
  1525. brinkmeyer
  1526. bristow
  1527. bristow
  1528. brittain
  1529. brittain
  1530. britton
  1531. britton
  1532. brockway
  1533. brodesser
  1534. brodesser
  1535. brodskaya
  1536. brodskaya
  1537. brodskaya
  1538. ratovskii
  1539. voronkov
  1540. broek
  1541. broggini
  1542. broggini
  1543. brook
  1544. brook
  1545. brook
  1546. henry
  1547. jueschkke
  1548. brookhart
  1549. brookhart
  1550. brookhart
  1551. green
  1552. brookhart
  1553. studabaker
  1554. brooks
  1555. brooks
  1556. iii//case
  1557. brooks
  1558. watson
  1559. broom
  1560. brossi
  1561. brossi
  1562. brotian
  1563. browm
  1564. brown
  1565. brown
  1566. brown
  1567. brown
  1568. brown
  1569. brown
  1570. brown
  1571. campbell
  1572. brown
  1573. jadhav
  1574. mandal
  1575. brown
  1576. krishnamurthy
  1577. brown
  1578. kulkarni
  1579. brown
  1580. midland
  1581. brown
  1582. ramachandran
  1583. brown
  1584. singaram
  1585. brown
  1586. brown
  1587. brown
  1588. brown
  1589. eastwood
  1590. brown
  1591. bennet
  1592. slebocka-tilk
  1593. brown
  1594. brown-wensley
  1595. brown-wensley
  1596. buchwald
  1597. canizzo
  1598. clawson
  1599. brownbridge
  1600. brownbridge
  1601. broxterman
  1602. bruce
  1603. bruce
  1604. bruce
  1605. swinger
  1606. bruce
  1607. white
  1608. bruckner
  1609. bruckner
  1610. brudsall
  1611. bruening
  1612. bruice
  1613. bruneau
  1614. bruneau
  1615. neveus
  1616. kabouche
  1617. ruppin
  1618. dixneuf
  1619. brunet
  1620. brunet
  1621. brunner
  1622. brunner
  1623. brunner
  1624. zettlmeier
  1625. brunvoll
  1626. brunvoll
  1627. cyvin
  1628. cyvin
  1629. bruson
  1630. bruson
  1631. bryan
  1632. bryce
  1633. bryce
  1634. bryce
  1635. becher
  1636. falt-hansen
  1637. bryce-smith
  1638. bryce-smith
  1639. gilbert
  1640. brycesmith
  1641. brycesmith
  1642. brycesmith
  1643. gilbert
  1644. brycki
  1645. bublitz
  1646. bublitz
  1647. rinehart
  1648. bubnov
  1649. bubnov
  1650. buchanan
  1651. buchanan
  1652. bucheister
  1653. bucher
  1654. buchwald
  1655. buchwald
  1656. buchwald
  1657. buchwald
  1658. isher
  1659. buckingham
  1660. buckingham
  1661. legon
  1662. roberts
  1663. buckman
  1664. buckman
  1665. bucourt
  1666. bucourt
  1667. heyde
  1668. mislow
  1669. budyka
  1670. budyka
  1671. kantor
  1672. alfimov
  1673. buehler
  1674. bueno
  1675. bueno
  1676. walsh
  1677. bukala
  1678. bulut
  1679. bumagin
  1680. bumagin
  1681. bunel
  1682. bunnelle
  1683. bunnelle
  1684. bunnett
  1685. bunnett
  1686. burdett
  1687. bures
  1688. bures
  1689. burger
  1690. burger
  1691. burgess
  1692. burgess
  1693. burgess
  1694. burgess
  1695. henderson
  1696. burgess
  1697. moyesherman
  1698. burgess
  1699. ohlmeyer
  1700. burgess
  1701. davies
  1702. skerlj
  1703. burgoyne
  1704. burgoyne
  1705. dixon
  1706. casey
  1707. burke
  1708. burke
  1709. burke
  1710. grieco
  1711. burkhardt
  1712. burkhardt
  1713. burkhardt
  1714. doney
  1715. slough
  1716. stack
  1717. heathcock
  1718. burns
  1719. burns
  1720. burrell
  1721. burrell
  1722. anthony
  1723. bursian
  1724. bursian
  1725. kogan
  1726. bursten
  1727. bursten
  1728. strittmatter
  1729. burton
  1730. burton
  1731. burton
  1732. morken
  1733. burwell
  1734. burwell
  1735. buscemi
  1736. buschmann
  1737. buschmann
  1738. scharf
  1739. hoffmann
  1740. esser
  1741. bushby
  1742. bushby
  1743. leyer
  1744. allen
  1745. buszek
  1746. buszek
  1747. butenschon
  1748. butenschon
  1749. butler
  1750. butler
  1751. butler
  1752. butler
  1753. oshea
  1754. butler
  1755. richard
  1756. roberts
  1757. butterworth
  1758. butterworth
  1759. hanessian
  1760. rytina
  1761. buyers
  1762. buyers
  1763. canty
  1764. honeyman
  1765. bzowej
  1766. bzowej
  1767. aballero
  1768. caballero
  1769. cabezas
  1770. cabezas
  1771. cabiddu
  1772. cabiddu
  1773. cablewski
  1774. cablewski
  1775. cabri
  1776. cabri
  1777. cacchi
  1778. cacchi
  1779. cacciapaglia
  1780. cacciapaglia
  1781. mandolini
  1782. cadogan
  1783. cadogan
  1784. cadogan
  1785. hickson
  1786. mcnab
  1787. cadogan
  1788. cahiez
  1789. cahiez
  1790. ingold
  1791. prelog
  1792. caine
  1793. caine
  1794. cainelli
  1795. cainelli
  1796. cainelli
  1797. panunzio
  1798. andreoli
  1799. martelli
  1800. spunta
  1801. giacomi
  1802. cairns
  1803. calabrese
  1804. callaway
  1805. callaway
  1806. callier
  1807. callier
  1808. caluwe
  1809. caluwe
  1810. johnson
  1811. cambie
  1812. cambie
  1813. cambie
  1814. rutledge
  1815. woodgab
  1816. caminade
  1817. caminade
  1818. majoral
  1819. caminade
  1820. majoral
  1821. mathieu
  1822. camou
  1823. campaigne
  1824. campaigne
  1825. schneller
  1826. campbell
  1827. campbell
  1828. sainsbury
  1829. searle
  1830. campi
  1831. campi
  1832. campora
  1833. campora
  1834. campora
  1835. paneque
  1836. poveda
  1837. carmona
  1838. canary
  1839. canary
  1840. canceill
  1841. canizzo
  1842. canty
  1843. canty
  1844. capella
  1845. capella
  1846. caplar
  1847. caplar
  1848. cornisso
  1849. sunjic
  1850. caple
  1851. capon
  1852. capon
  1853. siddhanta
  1854. zucco
  1855. capozzi
  1856. capozzi
  1857. capraro
  1858. capraro
  1859. schneider
  1860. caputo
  1861. caputo
  1862. carcanague
  1863. cardillo
  1864. cardillo
  1865. cardillo
  1866. orena
  1867. cardin
  1868. cardin
  1869. cardin
  1870. lappert
  1871. raston
  1872. cardin
  1873. cetinbaya
  1874. lappert
  1875. carless
  1876. carless
  1877. carlo
  1878. carlos
  1879. carlsen
  1880. carlsen
  1881. carmack
  1882. carmack
  1883. carmona
  1884. carnahan
  1885. carnahan
  1886. protasiewicz
  1887. lippard
  1888. carolyn
  1889. carpino
  1890. carpino
  1891. carreira
  1892. carreira
  1893. carreno
  1894. carrut
  1895. carrut
  1896. carson
  1897. carson
  1898. carstens
  1899. carstens
  1900. carter
  1901. carter
  1902. caruthers
  1903. caruthers
  1904. carver
  1905. carver
  1906. casara
  1907. casara
  1908. casaschi
  1909. casaschi
  1910. casey
  1911. casey
  1912. casiraghi
  1913. casiraghi
  1914. raghi
  1915. cason
  1916. cason
  1917. cassar
  1918. cassar
  1919. chiusoli
  1920. guerrieri
  1921. casson
  1922. casson
  1923. casteel
  1924. casteel
  1925. castro
  1926. castro
  1927. castro
  1928. castulik
  1929. catellani
  1930. catellani
  1931. catellani
  1932. chiusoli
  1933. catellani
  1934. chiusoli
  1935. costa
  1936. catena
  1937. catena
  1938. caton
  1939. caton
  1940. catsoulacos
  1941. catsoulacos
  1942. catsoulacos
  1943. catsoulacos
  1944. catsoulacos
  1945. catsoulacos
  1946. catsoulacos
  1947. catteau
  1948. caubere
  1949. caubere
  1950. caubere
  1951. cauci
  1952. caule
  1953. caule
  1954. furlani
  1955. sebald
  1956. caulfield
  1957. levinson
  1958. cavaleiro
  1959. cavaleiro
  1960. cavicchioni
  1961. cavicchioni
  1962. ceccherelli
  1963. ceccherelli
  1964. cecilia
  1965. cehulak
  1966. cekovic
  1967. celerier
  1968. celerier
  1969. cermak
  1970. cermak
  1971. cerny
  1972. cerny
  1973. cetinbaya
  1974. cettero
  1975. chakraborty
  1976. chakraborty
  1977. chakraborty
  1978. chakraborty
  1979. challand
  1980. chamberlin
  1981. chamberlin
  1982. bloom
  1983. chamberlin
  1984. chambers
  1985. chambron
  1986. chambron
  1987. dietrich-buchecker
  1988. sauvage
  1989. fleming
  1990. chandrasekhar
  1991. chandrasekhar
  1992. chandrasekhar
  1993. muralidhara
  1994. selvaraj
  1995. chandrasekharam
  1996. chang
  1997. chang
  1998. chanon
  1999. chanon
  2000. rajzmann
  2001. chanon
  2002. chapdelaine
  2003. chapdelaine
  2004. hulce
  2005. charette
  2006. holmes@
  2007. adlington
  2008. aitken
  2009. albericio@
  2010. alexakis
  2011. chuit
  2012. commercon-bourgain
  2013. foulon
  2014. jabri
  2015. alper
  2016. aoyama
  2017. arnett
  2018. aurich
  2019. babad@
  2020. bailey
  2021. patricia
  2022. bambino
  2023. barluenga
  2024. joglar
  2025. gonzalez
  2026. fustero
  2027. barton
  2028. bayer
  2029. begue
  2030. charpentier-morize
  2031. bennasar
  2032. lavil
  2033. alvarez
  2034. bosch
  2035. bernasconi
  2036. bhatt
  2037. black
  2038. blunden
  2039. cusack
  2040. smith
  2041. boger
  2042. bontagg
  2043. thomas
  2044. bowser
  2045. bregadze
  2046. brookhart
  2047. brown
  2048. bennet
  2049. slebocka-tilk
  2050. bublitz
  2051. rinehart
  2052. burgess
  2053. leyer
  2054. allen
  2055. cainelli
  2056. capozzi
  2057. casiraghi
  2058. celerier
  2059. acetic@
  2060. scand@
  2061. carbanion
  2062. chem@
  2063. detailed
  2064. react
  2065. hetero
  2066. chem@
  2067. nomet
  2068. chem@
  2069. advances
  2070. advances
  2071. photochemistry@
  2072. aldrichimica
  2073. aldrichimica
  2074. acta@
  2075. angew@
  2076. angew
  2077. engl@
  2078. carbocyclic
  2079. compounds
  2080. chemistry
  2081. applications
  2082. carboxylic
  2083. acids
  2084. carboxylic
  2085. derivatives
  2086. chemistry
  2087. chermistry
  2088. heterocyclic
  2089. compounds@
  2090. collect@
  2091. commun
  2092. compounds
  2093. comprehensive
  2094. comprehensive
  2095. heterocyclic
  2096. chemistry
  2097. charette
  2098. charette
  2099. mellon
  2100. rouillard
  2101. malenfant
  2102. charles
  2103. charles
  2104. marson
  2105. charlton
  2106. charlton
  2107. alauddin
  2108. charpentier-morize
  2109. charton
  2110. charton
  2111. charushin
  2112. charushin
  2113. alekseev
  2114. chupakhin
  2115. charushin
  2116. chupakhin
  2117. chatani
  2118. chatani
  2119. chatgilialoglu
  2120. chatgilialoglu
  2121. chatt
  2122. chatt
  2123. richards
  2124. chauhan
  2125. chauhan
  2126. chaussard
  2127. chaussard
  2128. folest
  2129. nedelec
  2130. perichon
  2131. sibille
  2132. chavan
  2133. chavan
  2134. cheikh
  2135. cheikh
  2136. chabouni
  2137. laurent
  2138. mison
  2139. nafti
  2140. chelain
  2141. chelucci
  2142. chelucci
  2143. chemin
  2144. chemin
  2145. scheffer
  2146. trotter
  2147. charette
  2148. charette
  2149. chiusoli
  2150. costa
  2151. pelizzi
  2152. ciapetti
  2153. cintas
  2154. cohen
  2155. coleman
  2156. comins
  2157. corey
  2158. corey
  2159. coxon
  2160. cristau@
  2161. curran
  2162. cymerman@
  2163. evans@
  2164. nagao
  2165. fujita
  2166. danishefsky
  2167. danishefsky
  2168. davies
  2169. keukeleire
  2170. dekhane
  2171. denmark
  2172. druliner@
  2173. duthaler
  2174. hafner
  2175. alsters
  2176. rothe
  2177. dyker
  2178. corey@
  2179. earl@
  2180. effenberger
  2181. ellis
  2182. engen
  2183. espenson@
  2184. evans
  2185. falbe
  2186. felix@
  2187. fischer
  2188. fleming
  2189. floss
  2190. strohl
  2191. franek
  2192. frenzel@
  2193. funke@
  2194. cheng
  2195. cheng
  2196. cherkashin
  2197. cherkasov
  2198. chernyshev
  2199. chernyshev
  2200. komalenkova
  2201. cheves
  2202. chevrier
  2203. chevrier
  2204. weiss
  2205. chiacchio
  2206. chiacchio
  2207. chiang
  2208. chiang
  2209. kresge
  2210. chiara
  2211. chiara
  2212. chiba
  2213. chibale
  2214. chibale
  2215. childs
  2216. childs
  2217. chimiak
  2218. chimiak
  2219. milewska
  2220. chimirri
  2221. chimirri
  2222. gitto
  2223. grasso
  2224. monforte
  2225. romeo
  2226. zappala
  2227. chimirri
  2228. grasso
  2229. zappala
  2230. chimizzi
  2231. chini
  2232. chini
  2233. chino
  2234. chino
  2235. chirnirri
  2236. chirnirri
  2237. gitto
  2238. grasso
  2239. monforte
  2240. romeo
  2241. zappala
  2242. chisholm
  2243. chisholm
  2244. chisholm
  2245. clark
  2246. hampden-smith
  2247. hoffman
  2248. chiu-yu
  2249. chiu-yu
  2250. huang
  2251. chiusoli
  2252. chiusoli
  2253. chiusoli
  2254. costa
  2255. pelizzi
  2256. chiusoli
  2257. costa
  2258. pelizzi
  2259. chkanikov
  2260. chmielewski
  2261. chojnowski
  2262. chojnowski
  2263. stanczyk
  2264. cholaphaneset
  2265. choudary
  2266. choudary
  2267. chowdhury
  2268. chowdhury
  2269. christensen
  2270. christensen
  2271. christopher
  2272. christou
  2273. chrzastek
  2274. chrzastek
  2275. lidia
  2276. chuang
  2277. chuang
  2278. chuit
  2279. chuit
  2280. corriu
  2281. young
  2282. chung
  2283. chung
  2284. schulz
  2285. chung
  2286. chupakhin
  2287. chupakhin
  2288. charushin
  2289. churms
  2290. churms
  2291. chuvatkin
  2292. chvertkina
  2293. chvertkina
  2294. khoklov
  2295. mironov
  2296. chwang
  2297. chwang
  2298. ciapetti
  2299. ciapetti
  2300. ciattini
  2301. ciattini
  2302. cicchi
  2303. ciganek
  2304. ciganek
  2305. cintas
  2306. cirillo
  2307. cirillo
  2308. panek
  2309. cirrincione
  2310. cirrincione
  2311. almerico
  2312. aiello
  2313. dattolo
  2314. citterio
  2315. citterio
  2316. ciufolini
  2317. clair
  2318. claramunt
  2319. claramunt
  2320. elguero
  2321. clardy
  2322. clark
  2323. clark
  2324. clark
  2325. kybett
  2326. macquarrie
  2327. clark
  2328. clarke
  2329. clarke
  2330. coates
  2331. lincoln
  2332. clausen
  2333. clausen
  2334. clausen
  2335. priess
  2336. clawson
  2337. clayden
  2338. clayden
  2339. clercq
  2340. clift
  2341. clissold
  2342. clissold
  2343. thickitt
  2344. clive
  2345. clive
  2346. clode
  2347. clode
  2348. closs
  2349. closs
  2350. clousse
  2351. coates
  2352. cocco
  2353. cocco
  2354. cohen
  2355. cohen
  2356. cohen
  2357. cohen
  2358. bhupathy
  2359. coleman
  2360. colin
  2361. collet
  2362. collet
  2363. dutasta
  2364. lozach
  2365. canceill
  2366. collin
  2367. collin
  2368. collin
  2369. collins
  2370. collins
  2371. sheldrake
  2372. crosby
  2373. collins
  2374. collins
  2375. djuric
  2376. collman
  2377. collman
  2378. collman
  2379. hegedus
  2380. norton
  2381. finke
  2382. collum
  2383. collum
  2384. colombani
  2385. colombani
  2386. colombo
  2387. colombo
  2388. colombo
  2389. zinczuk
  2390. ruveda
  2391. colonna
  2392. colonna
  2393. poloni
  2394. colquhoun
  2395. colquhoun
  2396. thompson
  2397. twigg
  2398. colvin
  2399. colvin
  2400. comasseto
  2401. comasseto
  2402. comins
  2403. comins
  2404. comins
  2405. comins
  2406. o'connor
  2407. commercon
  2408. commercon-bourgain
  2409. commins
  2410. condom
  2411. confalone
  2412. confalone
  2413. conia
  2414. conia
  2415. conia
  2416. perchec
  2417. conia
  2418. salaun
  2419. wintner
  2420. rebek
  2421. morgan
  2422. connelly
  2423. connelly
  2424. consiglio
  2425. consiglio
  2426. constable
  2427. constable
  2428. cooke
  2429. cooke
  2430. cooley
  2431. cooley
  2432. elvain
  2433. cooper
  2434. cooper
  2435. cooper
  2436. holmes
  2437. house
  2438. trumbull
  2439. coppola
  2440. coppola
  2441. coppola
  2442. schuster
  2443. corcoran
  2444. cordell
  2445. cordero
  2446. cordero
  2447. cordes
  2448. cordes
  2449. corey
  2450. corey
  2451. corey
  2452. cheng
  2453. corey
  2454. corey
  2455. gaspar
  2456. cornelis
  2457. cornelis
  2458. laszlo
  2459. cornelisse
  2460. cornelisse
  2461. cornelisse
  2462. havinga
  2463. cornisso
  2464. corriu
  2465. corriu
  2466. corriu
  2467. guerin
  2468. corriu
  2469. guerin
  2470. moreau
  2471. cossu
  2472. cossu
  2473. lucchi
  2474. fabbri
  2475. licini
  2476. pasquato
  2477. cossy
  2478. cossy
  2479. costa
  2480. costantini
  2481. costantini
  2482. costas
  2483. costero
  2484. costero
  2485. coulentianos
  2486. courtieu
  2487. courtieu
  2488. courtneidge
  2489. courtneidge
  2490. davies
  2491. cousins
  2492. cousins
  2493. coutts
  2494. coutts
  2495. coville
  2496. coxon
  2497. coxon
  2498. coxon
  2499. coxon
  2500. halton
  2501. coxon
  2502. james
  2503. coyle
  2504. coyle
  2505. crabb
  2506. crabb
  2507. crabb
  2508. jackson
  2509. patel
  2510. crabtree
  2511. crabtree
  2512. crabtree
  2513. cragg
  2514. cragg
  2515. craig
  2516. craig
  2517. craig
  2518. mellor
  2519. craine
  2520. craine
  2521. raban
  2522. crammer
  2523. crandall
  2524. crandall
  2525. crandall
  2526. apparu
  2527. creary
  2528. creary
  2529. crich
  2530. crich
  2531. crich
  2532. quintero
  2533. criegee
  2534. criegee
  2535. crimmins
  2536. crimmins
  2537. crimmins
  2538. reinhold
  2539. crisp
  2540. crisp
  2541. cristau
  2542. cristau
  2543. cristofoli
  2544. cristofoli
  2545. critchley
  2546. crombie
  2547. crombie
  2548. cromwell
  2549. cromwell
  2550. phillips
  2551. crosby
  2552. crosby
  2553. cross
  2554. cross
  2555. fyles
  2556. james
  2557. zojaji
  2558. crossley
  2559. crossley
  2560. crouse
  2561. crouse
  2562. crout
  2563. crout
  2564. macmanus
  2565. ricca
  2566. singh
  2567. critchley
  2568. gibso
  2569. crowe
  2570. crowe
  2571. crudden
  2572. crudden
  2573. glaenzer
  2574. csuzdi
  2575. csuzdi
  2576. cuether
  2577. cuether
  2578. cuevas
  2579. cullen
  2580. cullen
  2581. cunico
  2582. cunico
  2583. curci
  2584. curra
  2585. curra
  2586. curran
  2587. curran
  2588. curran
  2589. fevig
  2590. jasperse
  2591. totleb
  2592. curran
  2593. sisko
  2594. yeske
  2595. curran
  2596. curtin
  2597. cusack
  2598. cusmano
  2599. cutler
  2600. cutler
  2601. fleming
  2602. harley-mason
  2603. cyvin
  2604. czeskis
  2605. czeskis
  2606. ivanova
  2607. moiseenkov
  2608. nefedov
  2609. czewski
  2610. czugler
  2611. michael
  2612. jones
  2613. langley
  2614. seebach
  2615. d'angelo
  2616. d'angelo
  2617. d'angelo
  2618. desmaele
  2619. dumas
  2620. guingant
  2621. d'auria
  2622. williams
  2623. daboun
  2624. posner
  2625. nagao
  2626. fujita
  2627. dalla
  2628. dalla
  2629. dallas
  2630. dallas
  2631. dallemagne
  2632. dallemagne
  2633. dalpiaz
  2634. dalpiaz
  2635. damour
  2636. damour
  2637. damrauer
  2638. damrauer
  2639. robert
  2640. dandia
  2641. danelon
  2642. danelon
  2643. mascaretti
  2644. danheiser
  2645. danheiser
  2646. danieli
  2647. danieli
  2648. danishefsky
  2649. danishefsky
  2650. hefsky
  2651. danishefsky
  2652. danishevsky
  2653. danishevsky
  2654. danishevsky
  2655. dannecker
  2656. darbaruov
  2657. darbaruov
  2658. sundaramurthy
  2659. darensbourg
  2660. darensbourg
  2661. silva
  2662. springs
  2663. daszkiewicz
  2664. daszkiewicz
  2665. dattolo
  2666. dauben
  2667. dauben
  2668. dauria
  2669. daves
  2670. daves
  2671. hallberg
  2672. daves
  2673. david
  2674. david
  2675. shirley
  2676. david
  2677. maclean
  2678. david
  2679. rotella
  2680. david
  2681. gautheron
  2682. david
  2683. hanessian
  2684. david
  2685. warnhoff
  2686. davidson
  2687. davidson
  2688. davidson
  2689. preston
  2690. davidson
  2691. goodin
  2692. davies
  2693. davies
  2694. davies
  2695. davies
  2696. davies
  2697. green
  2698. davies
  2699. green
  2700. kelly
  2701. roberts
  2702. davies
  2703. davies
  2704. davies
  2705. donohoe
  2706. davies
  2707. donohoe
  2708. williams
  2709. davies
  2710. green
  2711. mingos
  2712. davies
  2713. mcnally
  2714. smallridge
  2715. davies-coleman
  2716. davies-coleman
  2717. rivett
  2718. davis
  2719. davis
  2720. anthony
  2721. cholaphaneset
  2722. davis
  2723. davis
  2724. davis
  2725. reddy
  2726. reddy
  2727. davis
  2728. sheppard
  2729. davis
  2730. belder
  2731. clercq
  2732. graauw
  2733. peters
  2734. vanbekkum
  2735. groot
  2736. keukeleire
  2737. kimpe
  2738. kimpe
  2739. verhe
  2740. lucchi
  2741. miotti
  2742. modena
  2743. lucchi
  2744. modena
  2745. lucchi
  2746. pasquato
  2747. mayer
  2748. meijere
  2749. meijere
  2750. meijere
  2751. meyer
  2752. meijere
  2753. wessjohann
  2754. mendoza
  2755. javier
  2756. mesmaaker
  2757. namor
  2758. lewis
  2759. schwing-weill
  2760. deboeck
  2761. deboeck
  2762. dechoux
  2763. dechoux
  2764. nazarenko
  2765. pashkevich
  2766. ponomarev
  2767. defoin
  2768. szafran
  2769. szafran
  2770. zofia
  2771. degenhardt
  2772. degl'innocenti
  2773. degussa
  2774. degussa
  2775. dehaen
  2776. dehaen
  2777. becher
  2778. dehiak-krook
  2779. dehmlow
  2780. dehmlow
  2781. dehmlow
  2782. dehmlow
  2783. dehni
  2784. dehni
  2785. dekhane
  2786. dekhane
  2787. dekimpe
  2788. dekimpe
  2789. deklera
  2790. deklera
  2791. forster
  2792. delaude
  2793. delaude
  2794. laszlo
  2795. smith
  2796. delbecq
  2797. delbecq
  2798. delgado
  2799. delgado
  2800. delia
  2801. delia
  2802. warner
  2803. della
  2804. della
  2805. deloisy
  2806. deloisy
  2807. delong
  2808. deloux
  2809. deloux
  2810. srebnik
  2811. demir
  2812. demir
  2813. demir
  2814. jeganathan
  2815. demuth
  2816. demuth
  2817. mikhail
  2818. denenmark
  2819. denholm
  2820. denicola
  2821. denicola
  2822. deninno
  2823. deninno
  2824. denis
  2825. denis
  2826. denise
  2827. denmark
  2828. dennis
  2829. denny
  2830. denny
  2831. nickon
  2832. derbesy
  2833. derbesy
  2834. derek
  2835. derkach
  2836. derkach
  2837. levchenko
  2838. derkach
  2839. levchenko
  2840. deroose
  2841. deroose
  2842. deryagina
  2843. deryagina
  2844. deryagina
  2845. voronkov
  2846. korchevin
  2847. desai
  2848. desai
  2849. desarbre
  2850. desarbre
  2851. descotes
  2852. descotes
  2853. deshpande
  2854. deshpande
  2855. deshpande
  2856. desilva
  2857. desilva
  2858. prasanna
  2859. desio
  2860. deslongchamps
  2861. ngchamps
  2862. deslongchamps
  2863. desmaele
  2864. desmaele
  2865. desmaison
  2866. desmaison
  2867. desmarteau
  2868. desmarteau
  2869. desouza
  2870. desouza
  2871. desponds
  2872. detar
  2873. detar
  2874. devan
  2875. devan
  2876. devery
  2877. devery
  2878. devlin
  2879. devlin
  2880. hargrave
  2881. devoe
  2882. devoe
  2883. olofson
  2884. sahyun
  2885. dewar
  2886. dewar
  2887. dewolfe
  2888. dewolfe
  2889. murphy
  2890. dharanipragada
  2891. dhawan
  2892. dhawan
  2893. dhillon
  2894. dhillon
  2895. dhokte
  2896. dhokte
  2897. dhokte
  2898. dianova
  2899. dianova
  2900. zabotina
  2901. jerry
  2902. dicke
  2903. dickens
  2904. dickens
  2905. gilday
  2906. negri
  2907. widdowson
  2908. dickinson
  2909. dickinson
  2910. dickson
  2911. dickson
  2912. didier
  2913. didier
  2914. diederich
  2915. diederich
  2916. isaacs
  2917. philp
  2918. diederich
  2919. diederich
  2920. rubin
  2921. diederich
  2922. smithrud
  2923. sanford
  2924. wyman
  2925. ferguson
  2926. diederich
  2927. whetten
  2928. diedrich
  2929. diedrich
  2930. dienst
  2931. dieter
  2932. dieter
  2933. dietrich
  2934. dietrich
  2935. sauvage
  2936. dietrich
  2937. viout
  2938. dietrich-buchecker
  2939. dilip
  2940. dillon
  2941. dillon
  2942. dilworth
  2943. dilworth
  2944. mckervey
  2945. dimaio
  2946. dimaio
  2947. rheingold
  2948. discordia
  2949. discordia
  2950. dishong
  2951. dittmer
  2952. dittmer
  2953. diversi
  2954. divona
  2955. divona
  2956. dixit
  2957. dixit
  2958. dixneuf
  2959. dixneuf
  2960. dixon
  2961. djerassi
  2962. djerassi
  2963. djerassi
  2964. djerassi
  2965. djerassi
  2966. silva
  2967. djuric
  2968. freedman
  2969. dobler
  2970. dockx
  2971. dockx
  2972. dodziuk
  2973. dodziuk
  2974. helena
  2975. doetz
  2976. doetz
  2977. doherty
  2978. doherty
  2979. hoffmann
  2980. dokichev
  2981. dokichev
  2982. dolbier
  2983. dolbier
  2984. doller
  2985. dolphin
  2986. dombrovskii
  2987. dominguez
  2988. dominguez
  2989. donal
  2990. donald
  2991. donaruma
  2992. donaruma
  2993. heldt
  2994. donati
  2995. donati
  2996. dondoni
  2997. dondoni
  2998. doney
  2999. donofrio
  3000. donohoe
  3001. donohoe
  3002. aleshkova
  3003. polimbetova
  3004. levina
  3005. petrova
  3006. dorfman
  3007. dorigo
  3008. dornsch
  3009. doroshkevich
  3010. doroshkevich
  3011. dorow
  3012. dorow
  3013. dorta
  3014. dorta
  3015. doubleday
  3016. doubleday
  3017. dougherty
  3018. dougherty
  3019. douglas
  3020. irngartinger
  3021. zhang
  3022. dowle
  3023. dowle
  3024. davies
  3025. downs
  3026. downs
  3027. pulham
  3028. doxsee
  3029. doxsee
  3030. mouser
  3031. farahi
  3032. doyle
  3033. doyle
  3034. drabowicz
  3035. drabowicz
  3036. kielbasinski
  3037. lyzwa
  3038. dragan
  3039. dragisich
  3040. dragisich
  3041. drake
  3042. drake
  3043. draper
  3044. drewes
  3045. drewes
  3046. drian
  3047. drone
  3048. drozdova
  3049. drueckhammer
  3050. drueckhammer
  3051. hennen
  3052. gautheron
  3053. druliner
  3054. druliner
  3055. stevens
  3056. dryuk
  3057. dryuk
  3058. dubac
  3059. dubac
  3060. laporterie
  3061. manuel
  3062. dubau
  3063. dubau
  3064. dubois
  3065. dubois
  3066. duburs
  3067. ducep
  3068. duchene
  3069. duchene
  3070. duchenet
  3071. duchenet
  3072. dueholm
  3073. dueholm
  3074. pedersen
  3075. duetsch
  3076. duetsch
  3077. duffy
  3078. duffy
  3079. dufour
  3080. dufour
  3081. dugas
  3082. dugas
  3083. dujardin
  3084. dujardin
  3085. dulcere
  3086. dulcere
  3087. pierre
  3088. dumas
  3089. dumont
  3090. rudorf
  3091. dunogues
  3092. dupoantier
  3093. dupoantier
  3094. dureault
  3095. durgaprasad
  3096. durgaprasad
  3097. durst
  3098. durst
  3099. durucasu
  3100. durucasu
  3101. dushin
  3102. dushin
  3103. dussault
  3104. dussault
  3105. dutasta
  3106. duthaler
  3107. duthaler
  3108. duthaler
  3109. hafner
  3110. duthaler
  3111. hafner
  3112. alsters
  3113. rothe
  3114. duthaler
  3115. hafner
  3116. riediker
  3117. duthaler
  3118. rudolf
  3119. dutta
  3120. dutta
  3121. dutton
  3122. dutton
  3123. dyakov
  3124. dyall
  3125. dyall
  3126. dyatkin
  3127. dyker
  3128. dyson
  3129. dzenis
  3130. dzhemilev
  3131. dzhemilev
  3132. corey
  3133. jacobsen
  3134. nakamura
  3135. smalley
  3136. suarez
  3137. tagliavini
  3138. vedejs
  3139. easton
  3140. easton
  3141. eastwood
  3142. eastwood
  3143. eaton
  3144. eaton
  3145. eaton
  3146. eberson
  3147. eberson
  3148. eberson
  3149. nyberg
  3150. ebert
  3151. ebert
  3152. ebert
  3153. ebetino
  3154. ebetino
  3155. degenhardt
  3156. jamieson
  3157. brudsall
  3158. ebihara
  3159. echavarren
  3160. echavarren
  3161. echer
  3162. echer
  3163. echeverria
  3164. eckstein
  3165. eckstein
  3166. edmonds
  3167. edmonds
  3168. francesconi
  3169. stick
  3170. edwards
  3171. edwards
  3172. edwin
  3173. effenberger
  3174. effenberger
  3175. effenberger
  3176. effenberger
  3177. efratz
  3178. efratz
  3179. eguchi
  3180. eguchi
  3181. matsushita
  3182. yamashita
  3183. eicher
  3184. eicher
  3185. weber
  3186. eichorn
  3187. einhorn
  3188. einhorn
  3189. einhorn
  3190. luche
  3191. eisch
  3192. eisch
  3193. eisch
  3194. sexsmith
  3195. eisch
  3196. shafii
  3197. boleslawski
  3198. eiter
  3199. eklund
  3200. eksterowicz
  3201. eksterowicz
  3202. ashry
  3203. mousaad
  3204. rashed
  3205. ashry
  3206. rashed
  3207. ramadan
  3208. khadem
  3209. el'tsov
  3210. el'tsov
  3211. el-rayyes
  3212. el-rayyes
  3213. al-awadi
  3214. elena
  3215. elgemeie
  3216. elgemeie
  3217. elgendy
  3218. elgendy
  3219. elguero
  3220. eliel
  3221. eliel
  3222. eliel
  3223. eliel
  3224. wilen
  3225. mander
  3226. elisa
  3227. ellatif
  3228. ellatif
  3229. eller
  3230. eller
  3231. schwarz
  3232. ellerd
  3233. elliott
  3234. elliott
  3235. ellis
  3236. ellis
  3237. ellis
  3238. romsey-alexander
  3239. ellis
  3240. ellison
  3241. ellison
  3242. ellsworth
  3243. ellsworth
  3244. elmoghayer
  3245. elnagdi
  3246. elnagdi
  3247. elmoghayer
  3248. sadek
  3249. elnagdi
  3250. sadek
  3251. elnagdi
  3252. shoig
  3253. mohareeb
  3254. elnagdi
  3255. mohamed
  3256. hilmy
  3257. elsayed
  3258. elsayed
  3259. elschenbroich
  3260. elschenbroich
  3261. salzer
  3262. elsevier
  3263. elsevier
  3264. muller
  3265. vrieze
  3266. elvain
  3267. elworthy
  3268. elworthy
  3269. emanuel
  3270. emanuel
  3271. dornsch
  3272. feger
  3273. frick
  3274. hergott
  3275. hofmann
  3276. emerson
  3277. emerson
  3278. eming
  3279. emrani
  3280. emsley
  3281. enders
  3282. enders
  3283. hasumi
  3284. engbersen
  3285. engdahl
  3286. engel
  3287. engel
  3288. engel
  3289. engels
  3290. engels
  3291. uhlmann
  3292. engen
  3293. engen
  3294. engewald
  3295. engewald
  3296. england
  3297. engler
  3298. engler
  3299. engman
  3300. engman
  3301. enholm
  3302. enholm
  3303. ennan
  3304. ephritikhine
  3305. ephritikhine
  3306. epsztajn
  3307. erber
  3308. erber
  3309. erdik
  3310. erdik
  3311. erdik
  3312. erfanian-abdoust
  3313. erian
  3314. erian
  3315. roskamp
  3316. eriksson
  3317. eriksson
  3318. erker
  3319. erker
  3320. erker
  3321. aulbach
  3322. pfaff
  3323. sosna
  3324. ernest
  3325. ernest
  3326. erzhanov
  3327. escalante
  3328. escalante
  3329. jaime
  3330. eschenmoser
  3331. eschenmoser
  3332. leowenthal
  3333. escribano
  3334. escribano
  3335. escudie
  3336. esipenko
  3337. esipenko
  3338. esipenko
  3339. samarai
  3340. esker
  3341. esker
  3342. esker
  3343. newcomb
  3344. espenson
  3345. espenson
  3346. esser
  3347. esser
  3348. pohlmann
  3349. scharf
  3350. estevez
  3351. estevez
  3352. eswarakrishnan
  3353. ettmayer
  3354. ettmayer
  3355. eusebio
  3356. evans
  3357. evans
  3358. andrews
  3359. evans
  3360. koelsch
  3361. evans
  3362. nelson
  3363. taber
  3364. evans
  3365. holmes
  3366. evans
  3367. evanseck
  3368. ewald
  3369. ewald
  3370. exner
  3371. enberg
  3372. dolbier
  3373. rstner
  3374. fabbri
  3375. faber
  3376. faber
  3377. faber
  3378. faber
  3379. fabian
  3380. fache
  3381. fache
  3382. fagan
  3383. fagan
  3384. calabrese
  3385. malone
  3386. fahey
  3387. fahey
  3388. faid-allah
  3389. falbe
  3390. falbe
  3391. falbe
  3392. falck
  3393. falck
  3394. falck
  3395. monteil
  3396. fallis
  3397. fallis
  3398. falt-hansen
  3399. falvey
  3400. fanta
  3401. fanta
  3402. farahi
  3403. farcasiu
  3404. farcasiu
  3405. balaban
  3406. bologna
  3407. farese
  3408. farina
  3409. farina
  3410. farina
  3411. farina
  3412. fasani
  3413. fasani
  3414. elisa
  3415. fathi
  3416. fathi
  3417. fatiadi
  3418. fatiadi
  3419. fatiadi
  3420. fattori
  3421. faulkner
  3422. faulkner
  3423. fedorova
  3424. fedorynski
  3425. feger
  3426. feher
  3427. fehlhammer
  3428. fehlhammer
  3429. fritz
  3430. galinder
  3431. feiken
  3432. feiken
  3433. feinauer
  3434. feinauer
  3435. feldman
  3436. felix
  3437. felix
  3438. felker
  3439. felkin
  3440. felkin
  3441. czewski
  3442. fenton
  3443. ferguson
  3444. feringa
  3445. feringa
  3446. lange
  3447. jansen
  3448. lubben
  3449. fernandez
  3450. fernandez
  3451. ferraboschi
  3452. ferraz
  3453. ferrier
  3454. ferrier
  3455. middleton
  3456. fetizon
  3457. fetizon
  3458. goulaovic
  3459. hanna
  3460. feuer
  3461. feuer
  3462. feuer
  3463. nielsen
  3464. fevig
  3465. fiandanese
  3466. fiandanese
  3467. fiaud
  3468. ficini
  3469. ficini
  3470. field
  3471. field
  3472. field
  3473. lamar
  3474. fieser
  3475. fieser
  3476. figadere
  3477. filippo
  3478. filippovich
  3479. filler
  3480. filler
  3481. fillippo
  3482. fillol
  3483. fillol
  3484. miranda
  3485. morera
  3486. sheikh
  3487. findeis
  3488. findeisen
  3489. findeisen
  3490. wagner
  3491. holtschmidt
  3492. finet
  3493. regitz
  3494. finke
  3495. fioravanti
  3496. firestone
  3497. firestone
  3498. fischer
  3499. fischer
  3500. fischer
  3501. bilha
  3502. fischer
  3503. fischer
  3504. fischer
  3505. fischer
  3506. fischer
  3507. weitz
  3508. fisher
  3509. fisher
  3510. fisher
  3511. muchowski
  3512. fitch
  3513. fitch
  3514. fitzgerald
  3515. fitzgerald
  3516. flack
  3517. flanagan
  3518. flanagan
  3519. joullie
  3520. flatt
  3521. flatt
  3522. fleet
  3523. fleet
  3524. flemin
  3525. fleming
  3526. fleming
  3527. fleming
  3528. fleming
  3529. dunogues
  3530. smithers
  3531. fleming
  3532. fletcher
  3533. flits
  3534. flits
  3535. flitsch
  3536. flitsch
  3537. flood
  3538. flood
  3539. florent
  3540. flores
  3541. florio
  3542. florio
  3543. floss
  3544. floss
  3545. floss
  3546. strohl
  3547. floss
  3548. strohl
  3549. flowers
  3550. floyd
  3551. floyd
  3552. flygare
  3553. fmann
  3554. fodor
  3555. fodor
  3556. dharanipragada
  3557. fodor
  3558. fumeau
  3559. sankaran
  3560. fodor
  3561. nagubandi
  3562. fokin
  3563. fokin
  3564. allakhverdiev
  3565. kolomiets
  3566. fokin
  3567. yutin
  3568. chkanikov
  3569. folest
  3570. foley
  3571. folkers
  3572. fontana
  3573. fontijn
  3574. fontijn
  3575. foote
  3576. foote
  3577. christopher
  3578. forman
  3579. forman
  3580. forster
  3581. forster
  3582. vogtle
  3583. fossey
  3584. fossey
  3585. lefort
  3586. sorba
  3587. fotsch
  3588. foubelo
  3589. foubelo
  3590. foulon
  3591. chanon
  3592. foxman
  3593. foxman
  3594. fraga
  3595. fraga
  3596. france
  3597. france
  3598. franceschi
  3599. francesconi
  3600. francheschi
  3601. francisco
  3602. francisco
  3603. franco
  3604. francois
  3605. francois
  3606. guibe
  3607. franek
  3608. franek
  3609. franek
  3610. frank
  3611. franklin
  3612. franklin
  3613. paterson
  3614. franz
  3615. franz-peter
  3616. franz-peter
  3617. montforts
  3618. franzini
  3619. fraser
  3620. fraser
  3621. fraser-reid
  3622. fraser-reid
  3623. merritt
  3624. handlon
  3625. andrews
  3626. fraser-reid
  3627. mootoo
  3628. konradsson
  3629. udodong
  3630. fraser-reid
  3631. udodong
  3632. ottosson
  3633. merritt
  3634. frauenrath
  3635. frauenrath
  3636. freccero
  3637. freccero
  3638. mauro
  3639. freche
  3640. frechet
  3641. frechet
  3642. frederickson
  3643. frederickson
  3644. freedman
  3645. freedman
  3646. freeman
  3647. freeman
  3648. freeman
  3649. rodriguez
  3650. freeman
  3651. hatlevig
  3652. freeman
  3653. peter
  3654. freeman
  3655. haynes
  3656. loughlin
  3657. mitchell
  3658. stokes
  3659. freidlina
  3660. freidlina
  3661. velichko
  3662. frenkel
  3663. frenkel
  3664. roganov
  3665. frenking
  3666. frenking
  3667. frenna
  3668. frenzel
  3669. frenzel
  3670. frick
  3671. fridman
  3672. fridman
  3673. surkov
  3674. novikov
  3675. friedrich
  3676. friedrich
  3677. friedrich
  3678. friesen
  3679. friesen
  3680. frimer
  3681. frimer
  3682. fringuelli
  3683. fringuelli
  3684. minuti
  3685. pizzo
  3686. taticchi
  3687. fringuelli
  3688. taticchi
  3689. fringuelli
  3690. taticchi
  3691. wenkert
  3692. fritz
  3693. froessl
  3694. frohlich
  3695. frohlich
  3696. frolova
  3697. froman
  3698. froman
  3699. fronza
  3700. fronza
  3701. fuganti
  3702. grasselli
  3703. pedrocchi
  3704. servi
  3705. frost
  3706. frost
  3707. frost
  3708. howarth
  3709. william
  3710. fryer
  3711. fryer
  3712. fryzuk
  3713. fryzuk
  3714. fuchigami
  3715. fuchigami
  3716. fuchigami
  3717. toshio
  3718. fuchs
  3719. fuchs
  3720. fuchs
  3721. fuganti
  3722. fuhrhop
  3723. fuhrhop
  3724. penzlin
  3725. fujii
  3726. fujii
  3727. fujii
  3728. yoshifuji
  3729. fujimoto
  3730. fujimoto
  3731. fujimura
  3732. fujimura
  3733. fujisaki
  3734. fujisaki
  3735. fujisawa
  3736. fujisawa
  3737. fujisawa
  3738. tamotsu
  3739. fujita
  3740. fujita
  3741. nagao
  3742. fujita
  3743. fujiwara
  3744. fujiwara
  3745. fujiwara
  3746. fukutani
  3747. hasegawa
  3748. maruoka
  3749. yamamoto
  3750. fujiwara
  3751. fujiwara
  3752. iintoku
  3753. takaki
  3754. fukuhara
  3755. fukuhara
  3756. fukumoto
  3757. fukumoto
  3758. fukutani
  3759. fukuto
  3760. fukuto
  3761. jensen
  3762. fukuyama
  3763. fukuyama
  3764. fumeau
  3765. fumie
  3766. fumie
  3767. fumio
  3768. funabiki
  3769. funabiki
  3770. funicello
  3771. funicello
  3772. spagnolo
  3773. zanirato
  3774. vollhardt
  3775. funke
  3776. funke
  3777. furin
  3778. furin
  3779. furlani
  3780. furlong
  3781. furstner
  3782. furukawa
  3783. furukawa
  3784. furuta
  3785. fuson
  3786. fuson
  3787. mckeever
  3788. fustero
  3789. fuxreiter
  3790. fuxreiter
  3791. fyles
  3792. gabbutt
  3793. gabbutt
  3794. gabriele
  3795. gabriele
  3796. gadaginamath
  3797. gadaginamath
  3798. gadamasetti
  3799. gaisina
  3800. galambos
  3801. galambos
  3802. galan
  3803. galan
  3804. amalia
  3805. galatsis
  3806. galatsis
  3807. galinder
  3808. galindo
  3809. gallagher
  3810. gallagher
  3811. galle
  3812. galle
  3813. galli
  3814. galli
  3815. galstyan
  3816. galvez
  3817. gambarotta
  3818. gambaryan
  3819. gamlath
  3820. gamlath
  3821. gammill
  3822. gammill
  3823. gandolfi
  3824. ganem
  3825. ganem
  3826. ganem
  3827. henion
  3828. ganesh
  3829. ganguly
  3830. meyers
  3831. thomas
  3832. gante
  3833. gante
  3834. ganushchak
  3835. garbesi
  3836. garbesi
  3837. gottarelli
  3838. mariani
  3839. spada
  3840. garcia
  3841. garcia
  3842. galvez
  3843. garegg
  3844. garegg
  3845. garin
  3846. garin
  3847. maire
  3848. garlaschelli
  3849. garlaschelli
  3850. garner
  3851. garner
  3852. garratt
  3853. garratt
  3854. garratt
  3855. payne
  3856. tsotinis
  3857. garst
  3858. garst
  3859. lattes
  3860. perie
  3861. gaspar
  3862. gasparini
  3863. gassman
  3864. gassman
  3865. gassman
  3866. tidwell
  3867. gasteiger
  3868. gatilov
  3869. gatilov
  3870. barkhash
  3871. gatto
  3872. gaudino
  3873. gaumont
  3874. gaumont
  3875. denis
  3876. gautheron
  3877. gauthier
  3878. gauthier
  3879. gautun
  3880. gautun
  3881. gawinecki
  3882. gawinecki
  3883. rasala
  3884. gawley
  3885. gazizov
  3886. gazizov
  3887. khairullin
  3888. moskva
  3889. gebicki
  3890. gebicki
  3891. geissman
  3892. geissman
  3893. gel'mbol'dt
  3894. gel'mbol'dt
  3895. ennan
  3896. gelas
  3897. gelas
  3898. gelbin
  3899. genet
  3900. genicot
  3901. gennari
  3902. gennari
  3903. gensier
  3904. gensier
  3905. geoffroy
  3906. geoffroy
  3907. bassner
  3908. geoffroy
  3909. bassner
  3910. geoffroy
  3911. sheridan
  3912. bassner
  3913. kelley
  3914. georg
  3915. georg
  3916. george
  3917. george
  3918. balachandran
  3919. gerasimov
  3920. gerasimov
  3921. parmon
  3922. gerasimova
  3923. gerasimova
  3924. kolchina
  3925. gerlach
  3926. gerlach
  3927. benjamin
  3928. german
  3929. german
  3930. mskov
  3931. german
  3932. zemskov
  3933. gerold
  3934. gerold
  3935. gerson
  3936. gerson
  3937. fabian
  3938. gerst
  3939. gerst
  3940. gerus
  3941. gheorghina
  3942. ghosez
  3943. ghosez
  3944. ghosez
  3945. genicot
  3946. gouverneur
  3947. ghosh
  3948. ghosh
  3949. ghosh
  3950. bandyopadhyay
  3951. maiti
  3952. ghosh
  3953. ghribi
  3954. giacometti
  3955. giacometti
  3956. giacomini
  3957. giannis
  3958. giannis
  3959. kolter
  3960. gibson
  3961. gibson
  3962. gibson
  3963. bradshaw
  3964. gielen
  3965. gielen
  3966. giese
  3967. giese
  3968. giese
  3969. giese
  3970. gilbert
  3971. gilbert
  3972. baggott
  3973. gilbert
  3974. gilbertson
  3975. gilbertson
  3976. gilchrist
  3977. gilchrist
  3978. gilchrist
  3979. moody
  3980. gilday
  3981. gilday
  3982. paquette
  3983. gilge
  3984. gilge
  3985. roesky
  3986. gillespie
  3987. gillespie
  3988. ramirez
  3989. marquarding
  3990. gilligan
  3991. gilligan
  3992. gillman
  3993. gilman
  3994. gilman
  3995. gingrich
  3996. gingrich
  3997. ghosh
  3998. huang
  3999. jones
  4000. ginsburg
  4001. ginsburg
  4002. ginzburg
  4003. ginzburg
  4004. giordano
  4005. giralt
  4006. girard
  4007. girreser
  4008. girreser
  4009. giuffrida
  4010. kohnke
  4011. mathias
  4012. philp
  4013. stodda
  4014. gitto
  4015. giudici
  4016. giuffrida
  4017. giuffrida
  4018. giuliano
  4019. giuliano
  4020. giumanini
  4021. giuseppe
  4022. giuseppe
  4023. bartoli
  4024. givens
  4025. givens
  4026. kueper
  4027. gladiali
  4028. gladiali
  4029. gladysz
  4030. gladysz
  4031. glaenzer
  4032. glasfeld
  4033. glass
  4034. glass
  4035. glass
  4036. glass
  4037. glebov
  4038. glebov
  4039. kliger
  4040. gleiter
  4041. gleiter
  4042. gleiter
  4043. kratz
  4044. gleiter
  4045. paquette
  4046. gleiter
  4047. schaefer
  4048. glenn
  4049. glinka
  4050. glukhovtsev
  4051. glukhovtsev
  4052. gneeva
  4053. gocmen
  4054. gocmen
  4055. bulut
  4056. godfrey
  4057. godfrey
  4058. goergens
  4059. goethe
  4060. goethe
  4061. gokel
  4062. gokel
  4063. gokel
  4064. arnold
  4065. delgado
  4066. echeverria
  4067. gatto
  4068. gustow
  4069. gokel
  4070. dishong
  4071. schultz
  4072. gatto
  4073. gokel
  4074. durst
  4075. gol'dshleger
  4076. gol'dshleger
  4077. moravskii
  4078. goldberg
  4079. goldberg
  4080. goldberg
  4081. goldberg
  4082. styrkovich
  4083. lukevics
  4084. goldmann
  4085. goldmann
  4086. stoltefuss
  4087. goldschmidt
  4088. goldschmidt
  4089. crammer
  4090. golebiowski
  4091. golebiowski
  4092. jurczak
  4093. gololobov
  4094. gololobov
  4095. kasukhin
  4096. gololobov
  4097. lysenko
  4098. boldeskul
  4099. golubev
  4100. golubev
  4101. kolomiets
  4102. fokin
  4103. gomez
  4104. gomez
  4105. gonzalez
  4106. gonzalez
  4107. galindo
  4108. mansilla
  4109. goodall
  4110. goodin
  4111. gooding
  4112. gooding
  4113. gorbatenko
  4114. gorbatenko
  4115. gorbatenko
  4116. samari
  4117. gorbovoi
  4118. gordeev
  4119. gordon
  4120. gordon
  4121. gordon
  4122. maskill
  4123. ruasse
  4124. gordon
  4125. gorecki
  4126. gorecki
  4127. gosney
  4128. ogawa
  4129. gottardo
  4130. gottardo
  4131. gottarelli
  4132. gottlieb
  4133. goulaovic
  4134. goumont
  4135. gourdoupis
  4136. gourdoupis
  4137. gouverneur
  4138. govindachari
  4139. graauw
  4140. graboski
  4141. grabowski
  4142. grachev
  4143. gracia
  4144. gracia
  4145. graczyk
  4146. graczyk
  4147. mikolajczyk
  4148. graczyk
  4149. piotr
  4150. graham
  4151. graham
  4152. grajkowski
  4153. grandjean
  4154. grandjean
  4155. grant
  4156. grant
  4157. grard
  4158. grasselli
  4159. grasso
  4160. grasso
  4161. zappala
  4162. chimizzi
  4163. gravel
  4164. graven
  4165. graven
  4166. gravestock
  4167. gravestock
  4168. grayson
  4169. grayson
  4170. graziani
  4171. grebenik
  4172. grebenik
  4173. grinter
  4174. perutz
  4175. greck
  4176. greck
  4177. green
  4178. green
  4179. mountford
  4180. green
  4181. lambeth
  4182. greenberg
  4183. greenberg
  4184. liebman
  4185. greenberg
  4186. greenberg//dolbier
  4187. greene
  4188. greene
  4189. greenhill
  4190. greenhill
  4191. greeves
  4192. greeves
  4193. gregory
  4194. grehn
  4195. greliermarly
  4196. greliermarly
  4197. grellier
  4198. grellier
  4199. grepioni
  4200. gribble
  4201. gribble
  4202. gridnev
  4203. gridnev
  4204. grieco
  4205. grieco
  4206. grieco
  4207. griengl
  4208. grierson
  4209. grierson
  4210. griesbeck
  4211. griesbeck
  4212. griffin
  4213. griffin
  4214. marchand
  4215. griffith
  4216. griffith
  4217. griffith
  4218. griffiths
  4219. griffiths
  4220. griffiths
  4221. griffiths
  4222. grifflths
  4223. grifflths
  4224. grigat
  4225. grigat
  4226. grigg
  4227. grigg
  4228. grigor'eva
  4229. grigor'eva
  4230. pinsker
  4231. grimes
  4232. grimes
  4233. grimm
  4234. grimmett
  4235. grimmett
  4236. grimmett
  4237. keene
  4238. grimmett
  4239. grinberg
  4240. grinberg
  4241. grinter
  4242. grisenti
  4243. grishchuk
  4244. grishchuk
  4245. gorbovoi
  4246. ganushchak
  4247. dombrovskii
  4248. grissom
  4249. schiess
  4250. grobel
  4251. grobel
  4252. seebach
  4253. groenen
  4254. groenen
  4255. gromov
  4256. gromov
  4257. gromov
  4258. groneberg
  4259. gronowitz
  4260. gronowitz
  4261. groot
  4262. groschl
  4263. groschl
  4264. gross
  4265. gross
  4266. gross
  4267. grossel
  4268. griffiths
  4269. grissom
  4270. grossel
  4271. weston
  4272. grundken@
  4273. guerriero
  4274. vigato
  4275. fenton
  4276. hellier
  4277. gukasyan@
  4278. rodney
  4279. kiplin@
  4280. brown@
  4281. werner//erker
  4282. haiduc
  4283. haner
  4284. hanessian
  4285. harris
  4286. hartwig
  4287. hashimoto
  4288. hayaishi
  4289. kondo
  4290. yoshikawa
  4291. heathcock
  4292. heimer@
  4293. hemmer@
  4294. herrmann
  4295. kohlpaintner
  4296. hirano@
  4297. hoffman
  4298. bartsch
  4299. holmes
  4300. ishida@
  4301. izatt
  4302. marshall@
  4303. jacobsen
  4304. jastrzebski@
  4305. johnson
  4306. jordan
  4307. bradley
  4308. lapointe
  4309. taylor
  4310. parker@
  4311. kadish
  4312. kalck
  4313. peres
  4314. jenck
  4315. kaneko@
  4316. kashima
  4317. katritzky
  4318. katritzky
  4319. grossel
  4320. weston
  4321. grotjahn
  4322. grotjahn
  4323. groutas
  4324. groutas
  4325. felker
  4326. grove
  4327. grove
  4328. grovenstein
  4329. grovenstein
  4330. groves
  4331. groves
  4332. grubbs
  4333. grubbs
  4334. undmann
  4335. grundmann
  4336. grushin
  4337. grushin
  4338. alper
  4339. grutzmacher
  4340. grutzmacher
  4341. gschwend
  4342. gschwend
  4343. rodriguez
  4344. guagano
  4345. guanti
  4346. guanti
  4347. giuseppe
  4348. gubnitskaya
  4349. gubnitskaya
  4350. peresypkina
  4351. samarai
  4352. gudat
  4353. guedj
  4354. guenard
  4355. guenard
  4356. gueritte-voegelein
  4357. potier
  4358. guenter
  4359. guenter
  4360. huthmacher
  4361. klenk
  4362. guenther
  4363. guenther
  4364. moskau
  4365. schmalz
  4366. guerchais
  4367. guerchais
  4368. guerin
  4369. gueritte-voegelein
  4370. guerrieri
  4371. guerriero
  4372. guerriero
  4373. vigato
  4374. fenton
  4375. hellier
  4376. guhrna
  4377. guibe
  4378. guibourdenche
  4379. guibourdenche
  4380. guijarro
  4381. guijarro
  4382. guijarro
  4383. guillanton
  4384. guilloton
  4385. guindon
  4386. guindon
  4387. guindon
  4388. anderson
  4389. yoakim
  4390. girard
  4391. berthiaume
  4392. morton
  4393. guingant
  4394. guinn
  4395. guitian
  4396. guitian
  4397. alstyan
  4398. avetisyan
  4399. gunaratne
  4400. gunaratne
  4401. gunaratne
  4402. nimal
  4403. gungor
  4404. gungor
  4405. gunther
  4406. gupta
  4407. gupta
  4408. snyder
  4409. gupta
  4410. guranowski
  4411. gusar
  4412. gusar
  4413. gusarova
  4414. gusarova
  4415. tatarinova
  4416. sinegovskaya
  4417. gusarova
  4418. voronkov
  4419. trofimov
  4420. gustowski
  4421. rogers
  4422. stewart
  4423. gutman
  4424. gutman
  4425. gutsche
  4426. gutsche
  4427. rodney
  4428. kiplin
  4429. guyot
  4430. guyot
  4431. guziec
  4432. guziec
  4433. fillippo
  4434. guzzo
  4435. guzzo
  4436. gyorgy
  4437. gyorkos
  4438. gyorkos
  4439. werner//erker
  4440. yamamoto
  4441. yamataka
  4442. h//van
  4443. haaland
  4444. haaland
  4445. habermas
  4446. habermas
  4447. denmark
  4448. jones
  4449. hachiya
  4450. hachiya
  4451. haddadin
  4452. haddadin
  4453. makhluf
  4454. hadjiarapoglou
  4455. hadjiarapoglou
  4456. hafner
  4457. hafner
  4458. lindner
  4459. meinhardt
  4460. hageman
  4461. hageman
  4462. hagemann
  4463. hagemann
  4464. hagemann
  4465. klamann
  4466. haider
  4467. haider
  4468. haider
  4469. heinisch
  4470. haiduc
  4471. haiduc
  4472. haiduc
  4473. haiduc
  4474. newton
  4475. haines
  4476. haines
  4477. halazy
  4478. halcrow
  4479. halcrow
  4480. christou
  4481. haley
  4482. hallberg
  4483. halpern
  4484. halpern
  4485. halterman
  4486. halterman
  4487. halton
  4488. halton
  4489. halton
  4490. stang
  4491. hamada
  4492. hamaguchi
  4493. hamilton
  4494. hamilton
  4495. morgan
  4496. hamlin
  4497. hamlin
  4498. weston
  4499. hammond
  4500. hamon
  4501. hampden-smith
  4502. hanack
  4503. hanack
  4504. hanaoka
  4505. hancock
  4506. handlon
  4507. haner
  4508. haner
  4509. haner
  4510. hanessian
  4511. hanford
  4512. hanford
  4513. sauer
  4514. hanna
  4515. schick
  4516. hans-gunther
  4517. hans-gunther
  4518. schmalz
  4519. hansen
  4520. hanson
  4521. hanson
  4522. hanson
  4523. oliveira
  4524. hanson
  4525. premuzic
  4526. hanson
  4527. hanusa
  4528. hanusa
  4529. haque
  4530. haque
  4531. harada
  4532. harada
  4533. harada
  4534. harald
  4535. harayama
  4536. hargrave
  4537. harikisan
  4538. hariri
  4539. hariri
  4540. harley-mason
  4541. harman
  4542. harman
  4543. gupta
  4544. brown
  4545. harmange
  4546. harmange
  4547. figadere
  4548. harmata
  4549. harmata
  4550. harms
  4551. harms
  4552. harnett
  4553. harnett
  4554. harper
  4555. harper
  4556. ohagan
  4557. harpp
  4558. harrington
  4559. harrington
  4560. harris
  4561. harris
  4562. harris
  4563. harris
  4564. harris
  4565. philip
  4566. harris
  4567. harris
  4568. harrowven
  4569. harrowven
  4570. hartenstein
  4571. hartenstein
  4572. hartke
  4573. hartke
  4574. hartley
  4575. hartley
  4576. hartley
  4577. patai
  4578. hartley
  4579. wiley
  4580. hartog
  4581. hartung
  4582. hartung
  4583. simonoff
  4584. hartwig
  4585. hartwig
  4586. harvey
  4587. harvey
  4588. harvey
  4589. harvey
  4590. harwood
  4591. harwood
  4592. hasega
  4593. hasegawa
  4594. haselba
  4595. hashimoto
  4596. hashimoto
  4597. hashimoto
  4598. haslam
  4599. haslam
  4600. haslam
  4601. edwin
  4602. hassall
  4603. hassall
  4604. hassel
  4605. hassenruck
  4606. hassenruck
  4607. martin
  4608. walsh
  4609. hasserck
  4610. hasserck
  4611. martin
  4612. hassner
  4613. hassner
  4614. hassner
  4615. fischer
  4616. hassner
  4617. stumer
  4618. hassner
  4619. alfred
  4620. hasumi
  4621. hasumi
  4622. hatakeyama
  4623. hatakeyama
  4624. hatanaka
  4625. hatanaka
  4626. hatanaka
  4627. hatanaka
  4628. hatanaka
  4629. hatanaka
  4630. hiyama
  4631. hatlevig
  4632. hatlevig
  4633. susan
  4634. hatsui
  4635. hatsui
  4636. haubenstock
  4637. haubenstock
  4638. haufe
  4639. haufe
  4640. hauser
  4641. hauser
  4642. hudson
  4643. hauser
  4644. swamer
  4645. adams
  4646. havinga
  4647. hawkins
  4648. hawkins
  4649. hawkins
  4650. hayaishi
  4651. hayaishi
  4652. kondo
  4653. yoshikawa
  4654. hayakawa
  4655. hayasaka
  4656. hayashi
  4657. hayashi
  4658. hayashi
  4659. hayashi
  4660. ozawa
  4661. hayashi
  4662. uozumi
  4663. hayashi
  4664. hayashida
  4665. hayashida
  4666. osamu
  4667. hayden
  4668. hayer
  4669. hayes
  4670. hayes
  4671. haynes
  4672. haynes
  4673. haywood-farmer
  4674. haywood-farmer
  4675. hazai
  4676. hazai
  4677. heaney
  4678. heaney
  4679. heathcock
  4680. heathcock
  4681. piettre
  4682. hechtberger
  4683. hedenstrom
  4684. hedenstrom
  4685. heffold
  4686. hegedus
  4687. hegedus
  4688. hegedus
  4689. hegedus
  4690. heicklen
  4691. heicklen
  4692. heigl
  4693. heilmayer
  4694. heimer
  4695. heimgartner
  4696. heimgartner
  4697. heinekey
  4698. heinekey
  4699. oldham
  4700. heinisch
  4701. heinisch
  4702. heldt
  4703. helena
  4704. hellier
  4705. helmchen
  4706. helmchen
  4707. gregory
  4708. henderson
  4709. henderson
  4710. hendrickson
  4711. hendrickson
  4712. hendrickson
  4713. sternbach
  4714. hendrix
  4715. henion
  4716. henne
  4717. henne
  4718. hennen
  4719. henning
  4720. henning
  4721. gelbin
  4722. henry
  4723. henry
  4724. reidel
  4725. herbert
  4726. herbert
  4727. herczegh
  4728. herge
  4729. herge
  4730. herges
  4731. herges
  4732. herges
  4733. rainer
  4734. hergott
  4735. hermanek
  4736. hermecz
  4737. hermecz
  4738. hermecz
  4739. kereszturi
  4740. hermes
  4741. hermez
  4742. hermez
  4743. kereszturi
  4744. vasvari-debreczy
  4745. hernandez
  4746. hernandez-mateo
  4747. herndon
  4748. herndon
  4749. krauzer
  4750. herndon
  4751. james
  4752. herrera
  4753. herrmann
  4754. herrmann
  4755. kohlpaintner
  4756. herscovici
  4757. herscovici
  4758. hertwig
  4759. hertwig
  4760. herunsalee
  4761. heskamp
  4762. hesse
  4763. hesse
  4764. hessen
  4765. hessen
  4766. teuben
  4767. heusler
  4768. hevesi
  4769. hewitt
  4770. hewitt
  4771. silvester
  4772. hewitt
  4773. hewlins
  4774. hewlins
  4775. olveira-campos
  4776. shannon
  4777. heyde
  4778. heyhawkins
  4779. heyhawkins
  4780. hibbert
  4781. hibbert
  4782. emsley
  4783. hibbert
  4784. hibino
  4785. hickson
  4786. hidai
  4787. hidai
  4788. mizobe
  4789. matsuzaka
  4790. hideg
  4791. hideg
  4792. hidemi
  4793. hiemstra
  4794. higuchi
  4795. higuchi
  4796. hiizu
  4797. hildebrandt
  4798. richards
  4799. saberi
  4800. thomas
  4801. hillers
  4802. hillgaertner
  4803. hilmy
  4804. hilvert
  4805. hilvert
  4806. hintze
  4807. hintze
  4808. hiraki
  4809. hiraki
  4810. hirama
  4811. hirama
  4812. hirama
  4813. hirano
  4814. hirano
  4815. hiraoka
  4816. hiraoka
  4817. hiroi
  4818. hiroi
  4819. hiroki
  4820. hiroki
  4821. yamanaka
  4822. hirose
  4823. hirota
  4824. hirsch
  4825. hirsch
  4826. hirsch
  4827. hirst
  4828. hirst
  4829. hisaeda
  4830. hisaeda
  4831. yoshio
  4832. hitchings
  4833. hitzler
  4834. hitzler
  4835. hixson
  4836. hixson
  4837. mariano
  4838. zimmmerman
  4839. hiyama
  4840. hiyama
  4841. fmann
  4842. hobza
  4843. hodge
  4844. hodge
  4845. sheringham
  4846. hodgetts
  4847. hodgetts
  4848. hodgson
  4849. hodgson
  4850. hoeper
  4851. hoeper
  4852. frank
  4853. hofer
  4854. hofer
  4855. hoffmaiester
  4856. hoffman
  4857. hoffman
  4858. hoffman
  4859. bartsch
  4860. hoffman
  4861. bartsch
  4862. hoffmann
  4863. hoffmann
  4864. hoffmann
  4865. hoffmann
  4866. hofle
  4867. hofle
  4868. steglich
  4869. vorbruggen
  4870. hofmann
  4871. hogen-esch
  4872. hogen-esch
  4873. hoimes
  4874. hoimes
  4875. hoiness
  4876. holcomb
  4877. holdt
  4878. holdt
  4879. holfe
  4880. holfe
  4881. holger
  4882. holland
  4883. holland
  4884. hollas
  4885. hollas
  4886. michael
  4887. hollis
  4888. hollis
  4889. holloway
  4890. holloway
  4891. melnik
  4892. holmes
  4893. holmes
  4894. holmquist
  4895. holmquist
  4896. wilson
  4897. nelson
  4898. holthausen
  4899. holthausen
  4900. holton
  4901. holton
  4902. holtschmidt
  4903. marcum
  4904. holzmeier
  4905. homma
  4906. homma
  4907. honda
  4908. honda
  4909. honeyman
  4910. honkawa
  4911. hoogsteen
  4912. hoogsteen
  4913. hooijdonk
  4914. hooijdonk
  4915. mander
  4916. witulski
  4917. hoppe
  4918. hoppe
  4919. hoppe
  4920. kraemer
  4921. schwark
  4922. zschage
  4923. horak
  4924. horak
  4925. horgan
  4926. horiuchi
  4927. horiuchi
  4928. akira
  4929. hornbuckle
  4930. horspool
  4931. horspool
  4932. armesto
  4933. horton
  4934. horton
  4935. hawkins
  4936. mcgarvey
  4937. horwell
  4938. horwell
  4939. hoshino
  4940. hoshino
  4941. hoskovec
  4942. hoskovec
  4943. hosmane
  4944. hosmane
  4945. maguire
  4946. hosokawa
  4947. hosokawa
  4948. hosokawa
  4949. murahashi
  4950. hosomi
  4951. hosomi
  4952. meier
  4953. vogtle
  4954. hostettmann
  4955. hough
  4956. evanseck
  4957. tucker
  4958. dorigo
  4959. houlihan
  4960. house
  4961. hoveyda
  4962. hoveyda
  4963. hoveyda
  4964. evans
  4965. howard
  4966. howard
  4967. alper
  4968. howarth
  4969. howells
  4970. howells
  4971. mccown
  4972. hsiao
  4973. hsiao
  4974. hsung
  4975. hsung
  4976. huang
  4977. huang
  4978. huang
  4979. huang
  4980. huang
  4981. huang
  4982. huang
  4983. huber
  4984. huber
  4985. huber
  4986. hubert
  4987. hubert
  4988. reimlinger
  4989. hudlicky
  4990. hudlicky
  4991. hudlicky
  4992. hudlicky
  4993. hudlicky
  4994. cehulak
  4995. hudlicky
  4996. olivo
  4997. price
  4998. hudlicky
  4999. gadamasetti
  5000. hudlicky
  5001. kutchan
  5002. naqvi
  5003. hudlicky
  5004. price
  5005. hudlicly
  5006. hudlicly
  5007. seoane
  5008. price
  5009. gadamasetti
  5010. hudrlik
  5011. hudrlik
  5012. hudrlik
  5013. hudson
  5014. hudson
  5015. hudson
  5016. huenig
  5017. huenig
  5018. huffm
  5019. huffm
  5020. hughes
  5021. hughes
  5022. hughes
  5023. david
  5024. hughes
  5025. huisgen
  5026. huisgen
  5027. huisgen
  5028. hulce
  5029. snyder
  5030. waghela
  5031. hulliger
  5032. hulliger
  5033. juerg
  5034. norin
  5035. hummer
  5036. hummer
  5037. humphries
  5038. hunig
  5039. hunig
  5040. muller
  5041. their
  5042. hunter
  5043. hunter
  5044. hunter
  5045. hunter
  5046. hurst
  5047. hurst
  5048. hurtaud
  5049. hurtaud
  5050. huryn
  5051. huryn
  5052. okabe
  5053. huskens
  5054. huskens
  5055. hussain
  5056. hussain
  5057. hussein
  5058. hussein
  5059. hussey
  5060. hutchins
  5061. hutchins
  5062. marygail
  5063. hutchins
  5064. hutchins
  5065. robert
  5066. hutchinson
  5067. hutchinson
  5068. hutchinson
  5069. huthmacher
  5070. huval
  5071. huval
  5072. huyser
  5073. huyser
  5074. gilbert
  5075. hyatt
  5076. hyatt
  5077. raynolds
  5078. hynes
  5079. hynes
  5080. ibarzo
  5081. ibarzo
  5082. ibata
  5083. ibata
  5084. ibuka
  5085. ibuka
  5086. ibuka
  5087. yamamoto
  5088. ichihara
  5089. ichihara
  5090. ichikawa
  5091. ichikawa
  5092. ichikawa
  5093. idacavage
  5094. iddon
  5095. iddon
  5096. iddon
  5097. ngochindo
  5098. ihara
  5099. ihara
  5100. fukumoto
  5101. iii//bates
  5102. iii//case
  5103. iii//hsu
  5104. iintoku
  5105. ikeda
  5106. ikeda
  5107. ikeda
  5108. ishibashi
  5109. ikeda
  5110. ikegami
  5111. ikramuddeen
  5112. ikramuddeen
  5113. ikuya
  5114. ilavsky
  5115. ilavsky
  5116. illuminati
  5117. illuminati
  5118. mandolini
  5119. imada
  5120. imada
  5121. imamoto
  5122. imamoto
  5123. imming
  5124. indolese
  5125. indolese
  5126. ingersoll
  5127. ingersoll
  5128. ingold
  5129. ingold
  5130. lusztyk
  5131. raner
  5132. inoguchi
  5133. inoguchi
  5134. sakuraba
  5135. achiwa
  5136. inoki
  5137. inoki
  5138. inokuchi
  5139. inokuma
  5140. inoue
  5141. inoue
  5142. inoue
  5143. seiichi
  5144. inoue
  5145. ioffe
  5146. ioganson
  5147. ipaktschi
  5148. ipaktschi
  5149. iqbal
  5150. iqbal
  5151. bhatia
  5152. nayyar
  5153. iqbal
  5154. javed
  5155. iranpoor
  5156. iranpoor
  5157. ireland
  5158. ireland
  5159. wyatt
  5160. ireland
  5161. irngartinger
  5162. irpichenko
  5163. isaacs
  5164. isaacs
  5165. isaka
  5166. isaka
  5167. iseki
  5168. iseki
  5169. isher
  5170. ishibashi
  5171. ishibashi
  5172. ishida
  5173. ishihara
  5174. ishihara
  5175. ishii
  5176. ishii
  5177. ishii
  5178. ishikura
  5179. ishikura
  5180. isimaru
  5181. isimaru
  5182. isobe
  5183. isobe
  5184. isobe
  5185. nishikawa
  5186. herunsalee
  5187. tsulciyama
  5188. hirose
  5189. isobe
  5190. nishikawa
  5191. yamamoto
  5192. tskiyama
  5193. okita
  5194. issberner
  5195. issberner
  5196. moors
  5197. vogtle
  5198. issidorides
  5199. issidorides
  5200. costas
  5201. gaudino
  5202. paulson
  5203. murakami
  5204. itokawa
  5205. itokawa
  5206. takeya
  5207. ittel
  5208. itzstein
  5209. ivanov
  5210. ivanova
  5211. iwakawa
  5212. iwakawa
  5213. iwamura
  5214. iwamura
  5215. iwamura
  5216. hiizu
  5217. iwamura
  5218. iwata
  5219. iwata
  5220. izatt
  5221. izatt
  5222. izatt
  5223. bradshaw
  5224. pawlak
  5225. bruening
  5226. tarbet
  5227. izatt
  5228. christensen
  5229. izatt
  5230. pawlak
  5231. bradshaw
  5232. bruening
  5233. izquierdo
  5234. izquierdo
  5235. medina
  5236. izumi
  5237. izumi
  5238. izumi
  5239. izutsu
  5240. izutsu
  5241. herndon
  5242. jabri
  5243. jabur
  5244. jabur
  5245. jackman
  5246. jackman
  5247. lange
  5248. jackson
  5249. jackson
  5250. angoh
  5251. jackson
  5252. jackson
  5253. james
  5254. jackson
  5255. jackson
  5256. jacob
  5257. jacob
  5258. jacobs
  5259. jacobs
  5260. jacobs
  5261. jacobsen
  5262. jacobsen
  5263. jacobsen
  5264. jacobsen
  5265. jacques
  5266. jacques
  5267. collet
  5268. wilen
  5269. jadhav
  5270. jaeger
  5271. jaeger
  5272. koehler
  5273. jager
  5274. jager
  5275. jaimala
  5276. jaime
  5277. jakob
  5278. jakubcova
  5279. jakubcova
  5280. jakubke
  5281. jalander
  5282. jalander
  5283. james
  5284. james
  5285. hough
  5286. james
  5287. resek
  5288. jamieson
  5289. jamison
  5290. jamison
  5291. janet
  5292. janet
  5293. grissom
  5294. janiak
  5295. janiak
  5296. schumann
  5297. jankowski
  5298. jankowski
  5299. raubo
  5300. wicha
  5301. janoschek
  5302. janoschek
  5303. janousek
  5304. jansen
  5305. jansen
  5306. jansen
  5307. groot
  5308. jaouen
  5309. jaouen
  5310. vessieres
  5311. butler
  5312. jaqueline
  5313. jaramillo
  5314. jaramillo
  5315. jaramillo
  5316. carlos
  5317. jarman
  5318. jarman
  5319. jasperse
  5320. jasperse
  5321. curran
  5322. fevig
  5323. jastrzebski
  5324. jastrzebski
  5325. h//van
  5326. koten
  5327. javed
  5328. javier
  5329. jaworek
  5330. d'angelo
  5331. piere
  5332. genet
  5333. jedlovska
  5334. jedlovska
  5335. jeevarajan
  5336. jeevarajan
  5337. jeffery
  5338. jeffery
  5339. jefford
  5340. jefford
  5341. jeganathan
  5342. jeker
  5343. jenck
  5344. jenkins
  5345. jenkins
  5346. jenkins
  5347. jennings
  5348. jennings
  5349. johnson
  5350. jensen
  5351. jensen
  5352. rickborn
  5353. jeong
  5354. jeong
  5355. jeong
  5356. jerome
  5357. jerry
  5358. jiang
  5359. jiang
  5360. jimenez
  5361. jimenez
  5362. jimenez-vazquez
  5363. bosch
  5364. joergen
  5365. joergensen
  5366. joergensen
  5367. schioett
  5368. joglar
  5369. johnson
  5370. johnson
  5371. johnson
  5372. johnson
  5373. johnson
  5374. johnson
  5375. adams
  5376. golebiowski
  5377. johnson
  5378. johnson
  5379. johnson
  5380. johnson
  5381. bethune
  5382. yannoni
  5383. johnson
  5384. johnson
  5385. johnson
  5386. johnston
  5387. johnston
  5388. jonas
  5389. jonas
  5390. jonathan
  5391. jonczyk
  5392. jonczyk
  5393. jones
  5394. jones
  5395. jones
  5396. jones
  5397. jones
  5398. greenhill
  5399. jones
  5400. jones
  5401. jones
  5402. bryan
  5403. jones
  5404. maitland
  5405. jones
  5406. desio
  5407. jones
  5408. jones
  5409. jones
  5410. gilman
  5411. jones
  5412. feher
  5413. jonge
  5414. jonsll
  5415. jordan
  5416. jordan
  5417. paddon-row
  5418. jordan
  5419. jordan
  5420. bradley
  5421. lapointe
  5422. taylor
  5423. jorgensen
  5424. jorgensen
  5425. jorgensen
  5426. jorgensen
  5427. hansen
  5428. becher
  5429. jorgensen
  5430. fischer
  5431. wimmer
  5432. joshi
  5433. joshi
  5434. joshi
  5435. dandia
  5436. sharma
  5437. joshi
  5438. joule
  5439. joule
  5440. joullie
  5441. joullie
  5442. thompson
  5443. juaristi
  5444. juaristi
  5445. juaristi
  5446. cuevas
  5447. juaristi
  5448. quintana
  5449. escalante
  5450. juaristi
  5451. eusebio
  5452. juerg
  5453. jueschkke
  5454. christensen
  5455. joergen
  5456. julia
  5457. julia
  5458. julius
  5459. juneja
  5460. beck-sickinger
  5461. jungheim
  5462. jungheim
  5463. shepherd
  5464. junjappa
  5465. junjappa
  5466. junjappa
  5467. asokan
  5468. junzo
  5469. juranic
  5470. juranic
  5471. jurczak
  5472. jurczak
  5473. baranowski
  5474. jurczak
  5475. golebiowski
  5476. jurczak
  5477. pikul
  5478. bauer
  5479. jurgens
  5480. jurgens
  5481. jursic
  5482. jursic
  5483. jutzi
  5484. jutzi
  5485. narasaka
  5486. vollhardt
  5487. feldman
  5488. takeda
  5489. tomioka
  5490. tritzky
  5491. kabachnik
  5492. kabalka
  5493. kabalka
  5494. kabalka
  5495. varma
  5496. kabbara
  5497. kabbara
  5498. kaberdin
  5499. kaberdin
  5500. potkin
  5501. kabouche
  5502. kadaba
  5503. kadaba
  5504. kadish
  5505. kadish
  5506. kadish
  5507. anderson
  5508. kadryov
  5509. kadryov
  5510. rokhlin
  5511. kaesz
  5512. kaesz
  5513. knobler
  5514. krone-schmidt
  5515. sieber
  5516. kagan
  5517. kagan
  5518. kagan
  5519. fiaud
  5520. kagan
  5521. kagan
  5522. rebiere
  5523. kagan
  5524. riant
  5525. kagan
  5526. sasaki
  5527. collin
  5528. kagan
  5529. michael
  5530. kahne
  5531. kahne
  5532. kaifer
  5533. wolfgang
  5534. kaiser
  5535. kaiser
  5536. kaiser
  5537. petty
  5538. knutson
  5539. kaiser
  5540. mihara
  5541. laforet
  5542. kelley
  5543. walters
  5544. findeis
  5545. kaiser
  5546. kaitmazova
  5547. kaitmazova
  5548. gambaryan
  5549. rokhlin
  5550. kajfez
  5551. kajigaeshi
  5552. kajimoto
  5553. kakusawa
  5554. kakusawa
  5555. kalck
  5556. kalck
  5557. peres
  5558. jenck
  5559. kalgutkar
  5560. kalgutkar
  5561. owski
  5562. kessler
  5563. kalinin
  5564. kalinin
  5565. kalinin
  5566. shilova
  5567. kaliya
  5568. kalka
  5569. kalvoda
  5570. kalvoda
  5571. heusler
  5572. kalyanaraman
  5573. kalyanaraman
  5574. george
  5575. kamal
  5576. kamal
  5577. kamal
  5578. sattur
  5579. kambouris
  5580. kamenecka
  5581. kamenecka
  5582. kamernitskii
  5583. kametani
  5584. kametani
  5585. kametani
  5586. hibino
  5587. kametani
  5588. honda
  5589. kametani
  5590. nemoto
  5591. kameyama
  5592. kameyama
  5593. kamigata
  5594. kamimura
  5595. kamimura
  5596. kamimura
  5597. kamlet
  5598. kamlet
  5599. kamochi
  5600. kamochi
  5601. kamura
  5602. kanda
  5603. kanda
  5604. kandad
  5605. kandad
  5606. kandanarachchi
  5607. kandanarachchi
  5608. bickelhaupt
  5609. singh
  5610. martin
  5611. doyle
  5612. kaneko
  5613. kaneko
  5614. kaneko
  5615. kanemasa
  5616. kanemasa
  5617. kanemasa
  5618. tsuge
  5619. kanematsu
  5620. kingsbury
  5621. blackburn
  5622. burton
  5623. kanner
  5624. kanner
  5625. kantlehner
  5626. kantlehner
  5627. funke
  5628. kantor
  5629. kappe
  5630. kappe
  5631. kappe
  5632. ziegler
  5633. kaprinidis
  5634. kaptein
  5635. karafiloglou
  5636. karaghiosoff
  5637. karakhanov
  5638. karakhanov
  5639. kelarev
  5640. polivin
  5641. karelson
  5642. karimov
  5643. karlsson
  5644. karpyshev
  5645. karpyshev
  5646. kartashov
  5647. kartashov
  5648. kartashov
  5649. skorobogatova
  5650. zefirov
  5651. kasai
  5652. kasai
  5653. kasatkin
  5654. kasatkin
  5655. tsypyshev
  5656. romanova
  5657. tolstikov
  5658. kashima
  5659. kashima
  5660. kaska
  5661. kasukhin
  5662. katagiri
  5663. katagiri
  5664. katayama
  5665. katayama
  5666. kathawala
  5667. kathawala
  5668. kathawala
  5669. coppola
  5670. schuster
  5671. ishida
  5672. katoh
  5673. katoh
  5674. nishio
  5675. kashima
  5676. katritzk
  5677. katritzk
  5678. katritzkcy
  5679. katritzky
  5680. katritzky
  5681. katritzky
  5682. katritzky
  5683. katritzky
  5684. brycki
  5685. katritzky
  5686. faid-allah
  5687. marson
  5688. katritzky
  5689. gordeev
  5690. katritzky
  5691. karelson
  5692. harris
  5693. katritzky
  5694. karelson
  5695. malhotra
  5696. katritzky
  5697. katritzky
  5698. katritzky
  5699. katritzky
  5700. marson
  5701. faid-allah
  5702. katritzky
  5703. rachwal
  5704. hitchings
  5705. katritzky
  5706. katritzky
  5707. katritzky
  5708. katritzsky
  5709. katritzsky
  5710. katritzsky
  5711. dennis
  5712. katrizky
  5713. katrizky
  5714. katsuhira
  5715. katsuhira
  5716. katsuki
  5717. katsurada
  5718. katsurada
  5719. kauffman
  5720. kauffman
  5721. wirthwein
  5722. kauffmann
  5723. kauffmann
  5724. kaufmann
  5725. kaufmann
  5726. schacht
  5727. kaufmann
  5728. kaupp
  5729. kaupp
  5730. kaupp
  5731. kausch
  5732. kawachi
  5733. kawachi
  5734. kawada
  5735. kawada
  5736. kawada
  5737. kawanami
  5738. kawanami
  5739. kawase
  5740. kearns
  5741. kearns
  5742. keefer
  5743. keefer
  5744. keene
  5745. keese
  5746. keese
  5747. keglevich
  5748. keglevich
  5749. keglevich
  5750. gyorgy
  5751. keiko
  5752. keiko
  5753. keiko
  5754. voronkov
  5755. keinan
  5756. keinan
  5757. keinan
  5758. keith
  5759. keith
  5760. buszek
  5761. kelarev
  5762. keller
  5763. keller
  5764. keller
  5765. neeland
  5766. rettig
  5767. trotter
  5768. weiler
  5769. kelley
  5770. kellie
  5771. kellie
  5772. riddell
  5773. kellogg
  5774. kellogg
  5775. kelly
  5776. kelly
  5777. kelly
  5778. kende
  5779. kende
  5780. kerber
  5781. kerber
  5782. kereszturi
  5783. baker
  5784. kerridge
  5785. kerridge
  5786. kessler
  5787. kessler
  5788. kevin
  5789. khadem
  5790. khaikin
  5791. khairullin
  5792. khairutdinov
  5793. khanapure
  5794. kharasch
  5795. kharasch
  5796. reinmuth
  5797. kharitonov
  5798. kharitonov
  5799. sobolev
  5800. panov
  5801. khaskin
  5802. khaskin
  5803. molodova
  5804. torgasheva
  5805. khenkin
  5806. khenkin
  5807. shilov
  5808. khlebnikov
  5809. khoklov
  5810. khripach
  5811. khristov
  5812. khristov
  5813. angelov
  5814. petrov
  5815. khumtaveeporn
  5816. khumtaveeporn
  5817. kibayashi
  5818. yashi
  5819. kielbasinski
  5820. kilburn
  5821. kilburn
  5822. patel
  5823. kilenyi
  5824. kilenyi
  5825. curran
  5826. angelici
  5827. sievers
  5828. kimpe
  5829. kimura
  5830. kimura
  5831. miller
  5832. schwartz
  5833. kingsbury
  5834. kingston
  5835. kingston
  5836. kingston
  5837. molinero
  5838. rimoldi
  5839. kinoshita
  5840. kinoshita
  5841. kinzy
  5842. kiplin
  5843. kiplinger
  5844. kiplinger
  5845. richmond
  5846. osterberg
  5847. kiplinger
  5848. jaqueline
  5849. kirby
  5850. kirby
  5851. kirby
  5852. kirillov
  5853. kirmse
  5854. kirmse
  5855. kirmse
  5856. wolfgang
  5857. kirsh
  5858. kirsh
  5859. smirnov
  5860. popkov
  5861. timashev
  5862. kirst
  5863. kirtane
  5864. kirwan
  5865. kirwan
  5866. kisch
  5867. kisch
  5868. holzmeier
  5869. kiselev
  5870. kiselev
  5871. konovalov
  5872. kishi
  5873. kislenko
  5874. kislenko
  5875. berlin
  5876. kitagawa
  5877. kitagawa
  5878. kitahara
  5879. kitahara
  5880. kitahara
  5881. kitamura
  5882. kitamura
  5883. kitano
  5884. kitano
  5885. kittaka
  5886. kittaka
  5887. klaas
  5888. klabunovskii
  5889. klabunovskii
  5890. klaffke
  5891. klair
  5892. klaman
  5893. klaman
  5894. klamann
  5895. klamann
  5896. klamann
  5897. klamann
  5898. hagemann
  5899. klapotke
  5900. klapotke
  5901. klarner
  5902. klarner
  5903. klaui
  5904. klaui
  5905. klaus
  5906. klausner
  5907. klausner
  5908. bodanshky
  5909. klausner
  5910. bodansky
  5911. klein
  5912. klein
  5913. klemchuk
  5914. klemm
  5915. klemm
  5916. klempier
  5917. klenk
  5918. klibanov
  5919. klibanov
  5920. kliger
  5921. klimo
  5922. kloetzel
  5923. kloetzel
  5924. kluger
  5925. klumpp
  5926. klumpp
  5927. klunder
  5928. klunder
  5929. zwanenburg
  5930. klundt
  5931. klundt
  5932. knapp
  5933. knapp
  5934. knapp
  5935. spencer
  5936. knight
  5937. knight
  5938. knight
  5939. knirel
  5940. knirel
  5941. vinogradov
  5942. knobler
  5943. knochel
  5944. knochel
  5945. rozema
  5946. tucker
  5947. retherford
  5948. furlong
  5949. knochel
  5950. singer
  5951. knoelker
  5952. knoelker
  5953. knolker
  5954. knolker
  5955. knolker
  5956. knops
  5957. knorr
  5958. knorr
  5959. knorre
  5960. knorre
  5961. fedorova
  5962. frolova
  5963. knowles
  5964. knowles
  5965. knowles
  5966. knutson
  5967. kobayash
  5968. kobayash
  5969. kobayashi
  5970. kobayashi
  5971. kobayashi
  5972. nakada
  5973. kobayashi
  5974. kober
  5975. kober
  5976. kobrich
  5977. kobrich
  5978. kratochvil
  5979. kvasnicka
  5980. matyska
  5981. pospichal
  5982. kocherkovet
  5983. kochetkov
  5984. kochetkov
  5985. kochi
  5986. kochi
  5987. kochi
  5988. bockman
  5989. kocienski
  5990. kocienski
  5991. kocienski
  5992. kocovsky
  5993. kocovsky
  5994. kodama
  5995. kodama
  5996. kodukulla
  5997. kodukulla
  5998. koehler
  5999. koelsch
  6000. koert
  6001. koert
  6002. koester
  6003. koester
  6004. yalpani
  6005. kogan
  6006. kohler
  6007. kohler
  6008. svennson
  6009. simon
  6010. kohlpaintner
  6011. kohnke
  6012. kohra
  6013. kohra
  6014. koichi
  6015. kolar
  6016. kolar
  6017. kobayashi
  6018. kobayeshi@
  6019. kolar
  6020. konig
  6021. koskinen
  6022. kozikowski
  6023. wetter
  6024. kreher
  6025. kropf
  6026. kulkarni
  6027. kuznets
  6028. kaliya
  6029. paquette@
  6030. lapucha@
  6031. lautens
  6032. lemmen
  6033. richter
  6034. werner
  6035. stumpf
  6036. lhommet@
  6037. likhotvorik
  6038. lipczynska-kochany
  6039. lloyd-williams@
  6040. lucchini
  6041. jung@
  6042. masatomo
  6043. iwao@
  6044. matsubara
  6045. mazeas@
  6046. mcmullen@
  6047. melikyan
  6048. meyers
  6049. miftakhov@
  6050. mingos@
  6051. miyake
  6052. moldvai@
  6053. moreno
  6054. morrison
  6055. mueller
  6056. mattay
  6057. mulzer
  6058. nagai
  6059. hamaguchi
  6060. naota
  6061. takeshi
  6062. negishi
  6063. ngochindo
  6064. nifant'ev
  6065. predvoditelev
  6066. kolar
  6067. kolbah
  6068. kolchina
  6069. koldobskii
  6070. koldobskii
  6071. koldobskii
  6072. ostrovskii
  6073. koljo
  6074. kollenz
  6075. kolodyazhnvi
  6076. kolodyazhnvi
  6077. kolomiets
  6078. kolter
  6079. kolycheva
  6080. komalenkova
  6081. komarov
  6082. komatsu
  6083. komatsu
  6084. komori
  6085. kompantseva
  6086. kondo
  6087. kondo
  6088. kondo
  6089. konig
  6090. konishi
  6091. konno
  6092. konovalov
  6093. konovalova
  6094. konradi
  6095. konradi
  6096. konradsson
  6097. koomen
  6098. koomen
  6099. kopach
  6100. kopach
  6101. kopecky
  6102. kopecky
  6103. korbonits
  6104. korbonits
  6105. korchevin
  6106. korchevin
  6107. koreeda
  6108. koreeda
  6109. korkin
  6110. korkin
  6111. kornblum
  6112. kornblum
  6113. korte
  6114. korth
  6115. koryta//dvorak
  6116. koser
  6117. koskimies
  6118. koskimies
  6119. koskinen
  6120. koskinen
  6121. koskinen
  6122. koskinen
  6123. kosolapoff
  6124. kosolapoff
  6125. gromov
  6126. sagitullin
  6127. kostikov
  6128. kostikov
  6129. molchanov
  6130. kostikov
  6131. molchanov
  6132. khlebnikov
  6133. kosyrev
  6134. kotali
  6135. kotali
  6136. kotali
  6137. harris
  6138. kotali
  6139. papageorgiou
  6140. kotali
  6141. tsoungas
  6142. kotali
  6143. antigoni
  6144. koten
  6145. kotera
  6146. kotera
  6147. kotha
  6148. kotha
  6149. kotsuki
  6150. kotsuki
  6151. kousuke
  6152. kousuke
  6153. harada
  6154. kouwenhoven
  6155. kovacs
  6156. kovacs
  6157. koval
  6158. koval
  6159. koval
  6160. kovalenko
  6161. kovrizhnykh
  6162. kovrizhnykh
  6163. shatenshtein
  6164. koyama
  6165. koyama
  6166. koyanagi
  6167. koyanagi
  6168. koz'min
  6169. kozhushko
  6170. kozhushko
  6171. lomakina
  6172. shokol
  6173. kozikowski
  6174. kozikowski
  6175. kozikowski
  6176. wetter
  6177. kozlowski
  6178. krach
  6179. kraemer
  6180. krafft
  6181. krafft
  6182. krakowiak
  6183. krakowiak
  6184. bradshaw
  6185. izatt
  6186. krakowiak
  6187. bradshaw
  6188. izatt
  6189. krakowiak
  6190. bradshaw
  6191. zamecka-krakowiak
  6192. kramer
  6193. kramer
  6194. krapcho
  6195. krapcho
  6196. krapcho
  6197. kratochvil
  6198. kratz
  6199. kraus
  6200. kraus
  6201. kraus
  6202. thomas
  6203. laramy
  6204. lirus
  6205. hanson
  6206. krause
  6207. krauzer
  6208. krebs
  6209. krebs
  6210. wilke
  6211. krechl
  6212. krechl
  6213. castulik
  6214. kreher
  6215. kreher
  6216. kreher
  6217. kreider
  6218. kresge
  6219. kresge
  6220. kricka
  6221. kricka
  6222. ledwith
  6223. krief
  6224. krief
  6225. krief
  6226. dumont
  6227. halazy
  6228. labar
  6229. laboureur
  6230. krief
  6231. hevesi
  6232. krief
  6233. laboureur
  6234. dumont
  6235. labar
  6236. krikorian
  6237. krikorian
  6238. krimen
  6239. krimen
  6240. krishna
  6241. krishna
  6242. krishnamurthy
  6243. krishnamurti
  6244. krishnamurti
  6245. krogelsch
  6246. krogh
  6247. krogh
  6248. krohn
  6249. krohn
  6250. krohn
  6251. kirst
  6252. krohnke
  6253. krohnke
  6254. kroker
  6255. tsvetkov
  6256. krone-schmidt
  6257. kropf
  6258. kropf
  6259. kropf
  6260. kropf
  6261. georg
  6262. thieme
  6263. verlag
  6264. kropf
  6265. schaumann
  6266. kroto
  6267. kroto
  6268. kroto
  6269. allaf
  6270. kroto
  6271. walton
  6272. kruger
  6273. krumpe
  6274. krutikov
  6275. krutosikova
  6276. krutosikova
  6277. krylov
  6278. krylov
  6279. krylov
  6280. krysan
  6281. krysan
  6282. kubas
  6283. kubas
  6284. kubota
  6285. kubota
  6286. kucera
  6287. kuczkowski
  6288. kuczkowski
  6289. kuehne
  6290. kuehne
  6291. kuell
  6292. kuell
  6293. kueper
  6294. kuhle
  6295. kuhle
  6296. kuhlmann
  6297. kuivila
  6298. kuivila
  6299. kuk'har
  6300. kuk'har
  6301. svistunova
  6302. solodenko
  6303. soloshonok
  6304. kukhar
  6305. kukhar
  6306. soloshonok
  6307. kukhar
  6308. yagupol'skii
  6309. gerus
  6310. kolycheva
  6311. kukhar
  6312. yagupol'skii
  6313. soloshonok
  6314. kukkola
  6315. kukkola
  6316. kukovinets
  6317. kukovinets
  6318. zainullin
  6319. tolstikov
  6320. kukushkin
  6321. kukushkin
  6322. kulinkovich
  6323. kulinkovich
  6324. kulkarni
  6325. kulkarni
  6326. dilip
  6327. kulkarni
  6328. kumabe
  6329. kumada
  6330. kumada
  6331. kumar
  6332. kumar
  6333. kumar
  6334. kumaran
  6335. kumaran
  6336. kumari
  6337. kumari
  6338. kundig
  6339. kundig
  6340. kunihiko
  6341. kupfer
  6342. kupfer
  6343. kurasawa
  6344. kuroda
  6345. kuroda
  6346. kurosawa
  6347. kurosawa
  6348. kuroyan
  6349. kuroyan
  6350. kurozumi
  6351. kurozumi
  6352. kursanov
  6353. kursanov
  6354. parnes
  6355. kurth
  6356. kurtz
  6357. kutateladze
  6358. kutateladze
  6359. zefirov
  6360. kutateladze
  6361. andrei
  6362. kutchan
  6363. kuthan
  6364. kuthan
  6365. sebek
  6366. kutyrev
  6367. kutyrev
  6368. kutyrev
  6369. kuwajima
  6370. kuwajima
  6371. kuwajima
  6372. kamura
  6373. kuwajima
  6374. nakamura
  6375. kuz'min
  6376. kuzmenko
  6377. kuzmenko
  6378. pozharskii
  6379. kuzmich
  6380. kuzmich
  6381. kuznets
  6382. kuznets
  6383. kaliya
  6384. kuznets
  6385. kaliya
  6386. kuznetsov
  6387. kuznetsov
  6388. zefirov
  6389. kuznetsov
  6390. shcherbakova
  6391. balaban
  6392. kuznetsov
  6393. ioffe
  6394. kvasnicka
  6395. kvittingen
  6396. kvittingen
  6397. kybett
  6398. kyler
  6399. kyoung
  6400. kyoung
  6401. kyriacos
  6402. hegedus
  6403. liebeskind
  6404. l'abbe
  6405. l'abbe
  6406. laarhoven
  6407. laarhoven
  6408. laatsch
  6409. laatsch
  6410. labadie
  6411. labadie
  6412. labar
  6413. labbe
  6414. labbe
  6415. labeish
  6416. labeish
  6417. petrov
  6418. labinger
  6419. lablache-combier
  6420. laboureur
  6421. ladlow
  6422. ladlow
  6423. laemmle
  6424. laemmle
  6425. lafont
  6426. laforet
  6427. manley
  6428. laidler
  6429. lakhlifi
  6430. lakhlifi
  6431. lalancette
  6432. lalancette
  6433. freche
  6434. brindle
  6435. lalonde
  6436. lalonde
  6437. breteler
  6438. arnason
  6439. hansen
  6440. lamar
  6441. lamara
  6442. lamara
  6443. lamarque
  6444. lamarque
  6445. lambert
  6446. lambert
  6447. schleyer
  6448. lambert
  6449. lambert
  6450. holcomb
  6451. magyar
  6452. lambeth
  6453. lammertsma
  6454. lammertsma
  6455. schleyer
  6456. schwarz
  6457. lampe
  6458. lampe
  6459. lancelot
  6460. lancelot
  6461. landais
  6462. landais
  6463. kabalka
  6464. lange
  6465. lange
  6466. langer
  6467. langer
  6468. langler
  6469. langler
  6470. langley
  6471. lanken
  6472. lansbury
  6473. lansbury
  6474. lantos
  6475. lantos
  6476. lapachev
  6477. lapachev
  6478. pebrenko
  6479. mamaev
  6480. lapidus
  6481. lapidus
  6482. pirozhkov
  6483. lapointe
  6484. laporta
  6485. laporterie
  6486. lapouyade
  6487. lapouyade
  6488. lappert
  6489. lappert
  6490. singh
  6491. lapucha
  6492. laramy
  6493. larock
  6494. larock
  6495. larock
  6496. richard
  6497. larson
  6498. larson
  6499. laschat
  6500. laschat
  6501. lasne
  6502. lasne
  6503. ripoll
  6504. laszlo
  6505. laszlo
  6506. lattes
  6507. launasmaa
  6508. launasmaa
  6509. mauri
  6510. laurent
  6511. lautens
  6512. lautos
  6513. lavelle
  6514. lavelle
  6515. lavil
  6516. lavilla
  6517. lavilla
  6518. lavrent'ev
  6519. lawrence
  6520. lawrence
  6521. jones
  6522. lawrence
  6523. lawson
  6524. lazar
  6525. lazar
  6526. rychly
  6527. klimo
  6528. pelikan
  6529. valko
  6530. guillanton
  6531. noble
  6532. leahy
  6533. leander
  6534. lebedev
  6535. leblanc
  6536. lebold
  6537. lebold
  6538. lebozec
  6539. lebozec
  6540. touchard
  6541. dixneuf
  6542. lectka
  6543. lednicer
  6544. lednicer
  6545. mitscher
  6546. georg
  6547. ledwith
  6548. grabowski
  6549. whitesides
  6550. lee-ruff
  6551. lee-ruff
  6552. leffler
  6553. leffler
  6554. leffler
  6555. lefort
  6556. lefrancois
  6557. legon
  6558. legzdins
  6559. legzdins
  6560. veltheer
  6561. lehmann
  6562. lehmkuhl
  6563. lehmkuhl
  6564. leitner
  6565. leitner
  6566. walter
  6567. lemenovskii
  6568. leming
  6569. lemmen
  6570. lemmen
  6571. richter
  6572. werner
  6573. stumpf
  6574. lemmen
  6575. richter
  6576. werner
  6577. stumpf
  6578. lenoir
  6579. lenoir
  6580. leonard
  6581. leonard
  6582. leone
  6583. leone
  6584. schleyer
  6585. leowenthal
  6586. leriverend
  6587. leriverend
  6588. lerner
  6589. lerner
  6590. benkovic
  6591. leskovsek
  6592. leskovsek
  6593. lesueur
  6594. lesueur
  6595. letard
  6596. letard
  6597. letourneau
  6598. leuenberger
  6599. leuenberger
  6600. leumann
  6601. levchenko
  6602. lever
  6603. lever
  6604. levina
  6605. levina
  6606. levinson
  6607. levitin
  6608. levkovskaya
  6609. bassani
  6610. reddy
  6611. lewis
  6612. lewis
  6613. lewis
  6614. rethwisch
  6615. denholm
  6616. norman
  6617. griffith
  6618. marsden
  6619. toogood
  6620. leyer
  6621. leznoff
  6622. leznoff
  6623. leznoff
  6624. lever
  6625. lhommet
  6626. lhommet
  6627. noble
  6628. purdy
  6629. liaaen-jensen
  6630. liaaen-jensen
  6631. lichtenthaler
  6632. lichtenthaler
  6633. licini
  6634. lickiss
  6635. lickiss
  6636. lidia
  6637. liebeskind
  6638. liebeskind
  6639. liebman
  6640. liebman
  6641. greenberg//dolbier
  6642. liebman
  6643. greenberg
  6644. dolbier
  6645. liebman
  6646. greenberg
  6647. dolbier
  6648. liebscher
  6649. liebscher
  6650. liganag
  6651. liganag
  6652. lijinsky
  6653. lijinsky
  6654. likholobov
  6655. likholobov
  6656. parmon
  6657. zamaraev
  6658. likhotvorik
  6659. likhotvorik
  6660. likhotvorik
  6661. lincoln
  6662. lindbe
  6663. lindbe
  6664. lindberg
  6665. lindberg
  6666. linderman
  6667. linderman
  6668. lindley
  6669. lindley
  6670. lindner
  6671. lindoy
  6672. lindoy
  6673. lindsay
  6674. lindsay
  6675. white
  6676. linford
  6677. linford
  6678. raubenheimer
  6679. lingibe
  6680. lingibe
  6681. linkov
  6682. liotta
  6683. liotta
  6684. liotta
  6685. lipczynska
  6686. lipczynska
  6687. lipczynska-kochany
  6688. lipczynska-kochany
  6689. lipkowitz
  6690. lipkowitz
  6691. peterson
  6692. lippard
  6693. lipschutz
  6694. lipschutz
  6695. lipshutz
  6696. lipshutz
  6697. lipshutz
  6698. lipshutz
  6699. lipshutz
  6700. sengupta
  6701. lipshutz
  6702. wilhelm
  6703. kozlowski
  6704. liras
  6705. liras
  6706. lirus
  6707. liska
  6708. liskamp
  6709. liskamp
  6710. liskamp
  6711. little
  6712. little
  6713. little
  6714. masjedizadeh
  6715. moeller
  6716. dannecker
  6717. litvinov
  6718. litvinovskaya
  6719. livinghouse
  6720. livingston
  6721. livingston
  6722. llace
  6723. lloyd
  6724. lloyd
  6725. lloyd
  6726. gosney
  6727. ormiston
  6728. lloyd
  6729. goodall
  6730. lloyd
  6731. mcnab
  6732. lloyd-williams
  6733. lloyd-williams
  6734. albericio
  6735. giralt
  6736. llups
  6737. lockhoff
  6738. lockhoff
  6739. loffler
  6740. loffler
  6741. lohray
  6742. lohray
  6743. lohray
  6744. bhushan
  6745. lolkema
  6746. lolkema
  6747. lomakina
  6748. fotsch
  6749. lopez
  6750. lopez
  6751. lopezherrera
  6752. lopezherrera
  6753. lorenz
  6754. lorimer
  6755. losler
  6756. lough
  6757. lough
  6758. loughlin
  6759. louis
  6760. louis
  6761. loupy
  6762. loupy
  6763. tchoubar
  6764. loutfy
  6765. lowinger
  6766. lowinger
  6767. william
  6768. lozach
  6769. lozach
  6770. lozinskii
  6771. lubben
  6772. lubineau
  6773. lubineau
  6774. lubineau
  6775. queneau
  6776. lucchi
  6777. lucchini
  6778. lucchini
  6779. luche
  6780. ludwig
  6781. ludwig
  6782. ludwig
  6783. luk'yanov
  6784. luk'yanova
  6785. lukacs
  6786. lukacs
  6787. lukacs
  6788. lukevics
  6789. lukevics
  6790. pudova
  6791. sturkovich
  6792. lukevics
  6793. zablocka
  6794. luknitskii
  6795. luknitskii
  6796. baizer
  6797. lusztyk
  6798. tietze
  6799. luzzio
  6800. luzzio
  6801. guziec
  6802. lynch
  6803. lynch
  6804. lyndsay
  6805. lysenko
  6806. lyzwa
  6807. yanoff
  6808. maryanoff
  6809. mackert
  6810. mackert
  6811. maclean
  6812. macmanus
  6813. macomber
  6814. macquarrie
  6815. madesclaire
  6816. madesclaire
  6817. madsen
  6818. madsen
  6819. maekawa
  6820. maekawa
  6821. maercker
  6822. maercker
  6823. maezaki
  6824. maezaki
  6825. magerlein
  6826. magid
  6827. magid
  6828. magnus
  6829. magnus
  6830. magnus
  6831. magnus
  6832. gallagher
  6833. browm
  6834. pappalardo
  6835. magnus
  6836. philip
  6837. magnusson
  6838. magnusson
  6839. maguire
  6840. maguire
  6841. glenn
  6842. magyar
  6843. mahadevan
  6844. mahadevan
  6845. maier
  6846. maier
  6847. maikap
  6848. maikap
  6849. maillard
  6850. maillard
  6851. lyndsay
  6852. maire
  6853. maiti
  6854. maiti
  6855. maiti
  6856. maitland
  6857. majcenlemarechal
  6858. majcenlemarechal
  6859. majetich
  6860. majetich
  6861. majewski
  6862. majewski
  6863. majid
  6864. majid
  6865. majoral
  6866. majoral
  6867. badri
  6868. caminade
  6869. majumdar
  6870. majumdar
  6871. makhluf
  6872. makin
  6873. makin
  6874. makin
  6875. makino
  6876. makioka
  6877. makioka
  6878. makosza
  6879. makosza
  6880. makosza
  6881. fedorynski
  6882. maksimenko
  6883. malacria
  6884. malacria
  6885. malek
  6886. malek
  6887. malek
  6888. malenfant
  6889. malhotra
  6890. malhotra
  6891. malisch
  6892. malisch
  6893. malkin
  6894. malkin
  6895. kuz'min
  6896. mallan
  6897. mallan
  6898. malone
  6899. malysheva
  6900. mamaev
  6901. manas
  6902. mancuso
  6903. mancuso
  6904. swern
  6905. mandai
  6906. mandal
  6907. mandel'shtam
  6908. mandel'shtam
  6909. mander
  6910. mander
  6911. mandolini
  6912. mandolini
  6913. mandon
  6914. manelis
  6915. manfred
  6916. mangeney
  6917. mangeney
  6918. manhas
  6919. manhas
  6920. wagle
  6921. chiang
  6922. manley
  6923. manly
  6924. manly
  6925. mansilla
  6926. manske
  6927. manske
  6928. kalka
  6929. mansuri
  6930. mansuy
  6931. mansuy
  6932. mantei
  6933. mantei
  6934. manuel
  6935. manzocchi
  6936. maragarita
  6937. marcaccini
  6938. marcaccini
  6939. torroba
  6940. march
  6941. marchand
  6942. marchand
  6943. marchand
  6944. brockway
  6945. marchetti
  6946. marcial
  6947. marcinow
  6948. marco
  6949. marco
  6950. ciufolini
  6951. marco-contelles
  6952. marco-contelles
  6953. marcocontelles
  6954. marcocontelles
  6955. marcum
  6956. marcus
  6957. marcus
  6958. marecek
  6959. marek
  6960. marek
  6961. maretina
  6962. maretina
  6963. margaretha
  6964. maria
  6965. maria
  6966. marian
  6967. mariani
  6968. mariano
  6969. mariano
  6970. mariella
  6971. marinetti
  6972. marinetti
  6973. marino
  6974. marino
  6975. marino
  6976. trudell
  6977. markaryan
  6978. markaryan
  6979. markaryan
  6980. samodurova
  6981. markies
  6982. markies
  6983. akkerman
  6984. bickelhaupt
  6985. smeets
  6986. marko
  6987. marko
  6988. marko
  6989. markovskii
  6990. markovskii
  6991. romanenko
  6992. marks
  6993. marks
  6994. markus
  6995. marotta
  6996. marquarding
  6997. marquart
  6998. marquart
  6999. marsais
  7000. marsden
  7001. marsha
  7002. marsha
  7003. marshall
  7004. marshall
  7005. marshall
  7006. marshman
  7007. marshman
  7008. marsi
  7009. marson
  7010. marson
  7011. marston
  7012. marston
  7013. hostettmann
  7014. martelli
  7015. martens
  7016. martin
  7017. martin
  7018. seoane
  7019. hanack
  7020. martin
  7021. seoane
  7022. hanack
  7023. martin
  7024. martin
  7025. martin
  7026. martin
  7027. guinn
  7028. martin
  7029. yvonne
  7030. martinelli
  7031. martinelli
  7032. martinez
  7033. martynov
  7034. martynov
  7035. yurtanov
  7036. marumo
  7037. marumo
  7038. maruoka
  7039. maruoka
  7040. maruoka
  7041. yamamoto
  7042. maruyama
  7043. maruyama
  7044. katagiri
  7045. marvell
  7046. marvell
  7047. marvell
  7048. maryanoff
  7049. maryanoff
  7050. maryanoff
  7051. maryanoff
  7052. reitz
  7053. maryanoff
  7054. marygail
  7055. marzilli
  7056. masaki
  7057. masamune
  7058. masamune
  7059. masamune
  7060. bates
  7061. corcoran
  7062. masamune
  7063. masamune
  7064. petersen
  7065. masanao
  7066. masanao
  7067. shimano
  7068. masao
  7069. masatomo
  7070. masatomo
  7071. masatoshi
  7072. mascal
  7073. mascal
  7074. mascarenas
  7075. mascarenas
  7076. mascaretti
  7077. mascaretti
  7078. mashkina
  7079. mashkina
  7080. masjedizadeh
  7081. maskill
  7082. maslak
  7083. maslak
  7084. przemyslaw
  7085. masler
  7086. masnyk
  7087. masnyk
  7088. mason
  7089. mason
  7090. mason
  7091. mason
  7092. lorimer
  7093. massacret
  7094. massacret
  7095. massey
  7096. massey
  7097. humphries
  7098. mastryukova
  7099. mastryukova
  7100. mastryukova
  7101. kabachnik
  7102. masuyama
  7103. masuyama
  7104. masuyama
  7105. yoshiro
  7106. mataga
  7107. mataga
  7108. matare
  7109. matare
  7110. matasi
  7111. matasi
  7112. julius
  7113. mathey
  7114. mathey
  7115. mathey
  7116. marinetti
  7117. mercier
  7118. mathias
  7119. mathias
  7120. stoddart
  7121. mathias
  7122. stoddart
  7123. mathias
  7124. mathieu
  7125. mathvink
  7126. mathvink
  7127. matlhav
  7128. matros
  7129. matsubara
  7130. matsubara
  7131. matsuda
  7132. matsuda
  7133. matsuda
  7134. matsuda
  7135. matsumoto
  7136. matsumoto
  7137. matsumoto
  7138. acheson
  7139. matsumoto
  7140. matsumoto
  7141. matsuo
  7142. matsuo
  7143. matsushita
  7144. matsushita
  7145. matsuura
  7146. matsuura
  7147. omura
  7148. matsuzaka
  7149. mattay
  7150. matteson
  7151. matteson
  7152. matthew
  7153. matveev
  7154. matveev
  7155. gorbatenko
  7156. samarai
  7157. matyska
  7158. mauder
  7159. mauder
  7160. harald
  7161. mauri
  7162. mauro
  7163. mavrov
  7164. maxwell
  7165. maxwell
  7166. mayer
  7167. mayer
  7168. mayer
  7169. kaska
  7170. mayon
  7171. mayon
  7172. hoffmaiester
  7173. baran
  7174. heigl
  7175. mazeas
  7176. mazeas
  7177. mazumdar
  7178. mazumdar
  7179. mazzucato
  7180. mazzucato
  7181. momicchioli
  7182. mcallister
  7183. mcallister
  7184. mccamley
  7185. mccarthy
  7186. mccarthy
  7187. mcclinton
  7188. mcclinton
  7189. mcclinton
  7190. mccombie
  7191. mccombie
  7192. ortiz
  7193. ganguly
  7194. mccown
  7195. mccoy
  7196. mccoy
  7197. colin
  7198. mcdaniel
  7199. mcdaniel
  7200. bradshaw
  7201. izatt
  7202. mcdonald
  7203. mcdonald
  7204. quentin
  7205. mcdonald
  7206. mcdonald
  7207. mcelvain
  7208. mcelvain
  7209. mcgaffin
  7210. mcgaffin
  7211. mcgarvey
  7212. mcgill
  7213. mcgill
  7214. rappa
  7215. mcglinchey
  7216. mcglinchey
  7217. mcgovern
  7218. mcgovern
  7219. vollhardt
  7220. mcgregor
  7221. mcgregor
  7222. sherrington
  7223. mckeever
  7224. mckervey
  7225. bohmer
  7226. mckew
  7227. mckew
  7228. mckillop
  7229. mckillop
  7230. mckillop
  7231. young
  7232. mckinney
  7233. mckinstry
  7234. mckinstry
  7235. mcmanus
  7236. mcmullen
  7237. mcmullen
  7238. leonard
  7239. mcmurray
  7240. mcmurray
  7241. mcmurry
  7242. mcmurry
  7243. mcmurry
  7244. lectka
  7245. mcmurry
  7246. raymond
  7247. smith
  7248. mcnab
  7249. mcnab
  7250. mcnally
  7251. mcnelis
  7252. mcnelis
  7253. mcomie
  7254. mcomie
  7255. blatchly
  7256. mcpherson
  7257. mcpherson
  7258. parish
  7259. mcquillin
  7260. mcquillin
  7261. mcquillin
  7262. parker
  7263. stephenson
  7264. medich
  7265. medina
  7266. meerpoel
  7267. meerpoel
  7268. mehlfuhrer
  7269. mehlfuhrer
  7270. mehra
  7271. mehrotra
  7272. mehrotra
  7273. singh
  7274. sogani
  7275. mehta
  7276. mehta
  7277. mehta
  7278. meier
  7279. meier
  7280. meier
  7281. zeller
  7282. meijer
  7283. meijere
  7284. meinhardt
  7285. meister
  7286. mekelburger
  7287. mekelburger
  7288. jaworek
  7289. vogtle
  7290. mekheimer
  7291. mekheimer
  7292. melcher
  7293. melcher
  7294. melikyan
  7295. melikyan
  7296. mella
  7297. mella
  7298. mariella
  7299. meller
  7300. meller
  7301. mellon
  7302. melloni
  7303. melloni
  7304. modena
  7305. tonellato
  7306. mellor
  7307. melnik
  7308. memmesheimer
  7309. memmesheimer
  7310. holger
  7311. memming
  7312. memming
  7313. rudiger
  7314. menchikov
  7315. menchikov
  7316. nefedov
  7317. mendenhall
  7318. mendenhall
  7319. mendoza
  7320. hesse
  7321. menger
  7322. menger
  7323. menicagli
  7324. mercier
  7325. merenyi
  7326. merenyi
  7327. stella
  7328. merkushev
  7329. merkushev
  7330. merlic
  7331. merritt
  7332. merritt
  7333. meskens
  7334. meskens
  7335. mesmaaker
  7336. mestroni
  7337. meth-cohn
  7338. meth-cohn
  7339. metwally
  7340. metzger
  7341. metzger
  7342. metzner
  7343. metzner
  7344. meunier
  7345. meunier
  7346. meyer
  7347. meyer
  7348. meyers
  7349. meyers
  7350. meyers
  7351. meyers
  7352. mihelich
  7353. meyerstein
  7354. meyerstein
  7355. mezey
  7356. mezey
  7357. mezhetritskii
  7358. mezhetritskii
  7359. tkachenko
  7360. mianowska
  7361. michael
  7362. michael
  7363. michael
  7364. pirrung
  7365. michael
  7366. michael
  7367. pattenden
  7368. michael
  7369. rachita
  7370. michael
  7371. rathke
  7372. michalska
  7373. michalska
  7374. michalski
  7375. michalski
  7376. micheli
  7377. michl
  7378. michl
  7379. bonacic-koutecky
  7380. michl
  7381. middlemiss
  7382. middlemiss
  7383. watson
  7384. middleton
  7385. midland
  7386. midland
  7387. midura
  7388. mielniczak
  7389. mielniczak
  7390. marian
  7391. miftakhov
  7392. miftakhov
  7393. valeev
  7394. gaisina
  7395. miginiac
  7396. miginiac
  7397. mihailovic
  7398. mihailovic
  7399. cekovic
  7400. mihara
  7401. mihelich
  7402. jonge
  7403. mikami
  7404. mikami
  7405. nakai
  7406. mikami
  7407. shimizu
  7408. mikami
  7409. terada
  7410. narisawa
  7411. nakai
  7412. mikami
  7413. koichi
  7414. mikhail
  7415. mikhaleva
  7416. mikolajczyk
  7417. mikolajczyk
  7418. mikolajczyk
  7419. drabowicz
  7420. mikolajczyk
  7421. kielbasinski
  7422. mikolajczyk
  7423. marian
  7424. milewska
  7425. millard
  7426. miller
  7427. miller
  7428. miller
  7429. miller
  7430. miller
  7431. miller
  7432. miller
  7433. mills
  7434. miltz
  7435. miltz
  7436. minale
  7437. minale
  7438. riccio
  7439. zollo
  7440. minami
  7441. minami
  7442. motoyoshiya
  7443. minamikawa
  7444. mingos
  7445. minisci
  7446. minisci
  7447. minisci
  7448. cettero
  7449. giordano
  7450. minisci
  7451. vismara
  7452. fontana
  7453. minkin
  7454. mintz
  7455. mintz
  7456. minuti
  7457. mioskowski
  7458. mioskowski
  7459. miranda
  7460. miranda
  7461. miranda
  7462. garcia
  7463. mironov
  7464. mironov
  7465. miroslaw
  7466. mirskova
  7467. mirskova
  7468. drozdova
  7469. levkovskaya
  7470. voronkov
  7471. mirskova
  7472. seredkina
  7473. voronkov
  7474. mirzaei
  7475. mirzaei
  7476. yousef
  7477. misicvukovic
  7478. misicvukovic
  7479. mislow
  7480. mislow
  7481. mison
  7482. mitani
  7483. mitani
  7484. mitchell
  7485. mitchell
  7486. mitchell
  7487. mitchell
  7488. mitchell
  7489. mitscher
  7490. mitsudo
  7491. mitsudo
  7492. watanabe
  7493. mitsunobu
  7494. mitsunobu
  7495. mitzel
  7496. mitzel
  7497. miura
  7498. miura
  7499. miyake
  7500. miyake
  7501. miyashi
  7502. miyashi
  7503. ikeda
  7504. konno
  7505. okitsu
  7506. takahashi
  7507. miyashita
  7508. miyaura
  7509. miyaura
  7510. miyazaki
  7511. miyazaki
  7512. miyazawa
  7513. mizhiritskii
  7514. mizobe
  7515. mizojiri
  7516. mizojiri
  7517. mizuno
  7518. mizuno
  7519. otsuji
  7520. mizuno
  7521. kazuhiko
  7522. mkrtchyan
  7523. mocerino
  7524. mocerino
  7525. modena
  7526. modena
  7527. tonellati
  7528. moderhack
  7529. moderhack
  7530. moderhack
  7531. dietrich
  7532. tarak
  7533. moeller
  7534. mohamed
  7535. mohareb
  7536. mohareb
  7537. mohareeb
  7538. mohiuddin
  7539. mohiuddin
  7540. satyanarayana
  7541. ahmed
  7542. ratnam
  7543. mohring
  7544. mohring
  7545. coville
  7546. moiseenkov
  7547. moiseenkov
  7548. dragan
  7549. veselovskii
  7550. moiseev
  7551. moiseev
  7552. mokhallalati
  7553. mokhallalati
  7554. mokrushin
  7555. molander
  7556. molchanov
  7557. moldvai
  7558. moldvai
  7559. molina
  7560. molina
  7561. molina
  7562. vilaplana
  7563. molinero
  7564. molinski
  7565. molinski
  7566. moller
  7567. molloy
  7568. molloy
  7569. molodova
  7570. momicchioli
  7571. momose
  7572. momose
  7573. momose
  7574. takefumi
  7575. monforte
  7576. moniatte
  7577. moniatte
  7578. monneret
  7579. monneret
  7580. florent
  7581. montauflier
  7582. montauflier
  7583. monteil
  7584. monteiro
  7585. monteiro
  7586. montforts
  7587. montforts
  7588. gerlach
  7589. hoeper
  7590. montforts
  7591. franz
  7592. peter
  7593. montgomery
  7594. montgomery
  7595. monti
  7596. monti
  7597. moody
  7598. moody
  7599. moody
  7600. moore
  7601. moore
  7602. moore
  7603. moorefield
  7604. moors
  7605. mootoo
  7606. moravskii
  7607. mordini
  7608. moreau
  7609. moreau
  7610. moreno
  7611. moreno
  7612. moreno
  7613. manas
  7614. marcial
  7615. moreno-manas
  7616. moreno-manas
  7617. pleixatz
  7618. morera
  7619. moret
  7620. morgan
  7621. watanabe
  7622. moriarty
  7623. moriarty
  7624. moriarty
  7625. moriarty
  7626. prakash
  7627. moriarty
  7628. moriarty
  7629. koser
  7630. morimoto
  7631. morimoto
  7632. chiba
  7633. achiwa
  7634. morimoto
  7635. takashi
  7636. morin
  7637. morin
  7638. moritani
  7639. moritani
  7640. fujiwara
  7641. moriya
  7642. moriya
  7643. morken
  7644. morken
  7645. morkved
  7646. morkved
  7647. morrill
  7648. morrill
  7649. morris
  7650. morris
  7651. morrison
  7652. morrison
  7653. morrison
  7654. morrison
  7655. morrison
  7656. morrison
  7657. masler
  7658. newbury
  7659. morrison
  7660. scott
  7661. mortier
  7662. morton
  7663. moset
  7664. moset
  7665. mozingo
  7666. mosettig
  7667. mosettig
  7668. moskau
  7669. moskva
  7670. robert
  7671. motallebi
  7672. motherwell
  7673. motherwell
  7674. crich
  7675. motherwell
  7676. nutley
  7677. motohashi
  7678. motohashi
  7679. emrani
  7680. meyer
  7681. kawase
  7682. motohashi
  7683. kawase
  7684. emrani
  7685. motoi
  7686. motokazu
  7687. motoyoshiya
  7688. moulines
  7689. mountford
  7690. mousaad
  7691. mouser
  7692. moussounga
  7693. moussounga
  7694. moutet
  7695. moutet
  7696. mouzin
  7697. moyesherman
  7698. mozingo
  7699. msayib
  7700. msayib
  7701. mskov
  7702. muchowski
  7703. mudryk
  7704. mudryk
  7705. mueller
  7706. mueller
  7707. mattay
  7708. muellerwesterhoff
  7709. muellerwesterhoff
  7710. muellerwesterhoff
  7711. muetterties
  7712. muetterties
  7713. bleeke
  7714. mujica
  7715. mujica
  7716. mukai
  7717. mukai
  7718. murakami
  7719. mukai
  7720. mukaiyama
  7721. iyama
  7722. mukaiyama
  7723. mukaiyama
  7724. kobayashi
  7725. mukaiyama
  7726. teruaki
  7727. mukerjee
  7728. mukerjee
  7729. mukerjee
  7730. ashare
  7731. mukerjee
  7732. srivastava
  7733. mukherjee
  7734. mukherjee
  7735. mukherjee
  7736. mukiayama
  7737. mukiayama
  7738. teruaki
  7739. mullen
  7740. mullen
  7741. klaus
  7742. muller
  7743. muller
  7744. muller
  7745. seebach
  7746. muller
  7747. muller
  7748. mulzer
  7749. mulzer
  7750. mulzer
  7751. mundy
  7752. mundy
  7753. ellerd
  7754. munehiro
  7755. munehiro
  7756. nakatani
  7757. murahashi
  7758. murahashi
  7759. murahashi
  7760. naota
  7761. murahashi
  7762. murahashi
  7763. murai
  7764. sonoda
  7765. murai
  7766. toshiaki
  7767. murakami
  7768. murakami
  7769. murakami
  7770. yukito
  7771. muralidhara
  7772. muraoka
  7773. muraoka
  7774. murata
  7775. murata
  7776. murata
  7777. murayama
  7778. murayama
  7779. murphree
  7780. murphy
  7781. murphy
  7782. murphy
  7783. murphy
  7784. brennan
  7785. murray
  7786. murray
  7787. murray
  7788. murray
  7789. murray
  7790. william
  7791. murry
  7792. mutter
  7793. mutter
  7794. vuilleumier
  7795. muzart
  7796. muzart
  7797. myers
  7798. myers
  7799. krause
  7800. bauld
  7801. sonoda
  7802. yoshioka
  7803. naddaka
  7804. naddaka
  7805. sadekov
  7806. maksimenko
  7807. minkin
  7808. nader
  7809. nader
  7810. nadler
  7811. nadler
  7812. william
  7813. naeva
  7814. nafti
  7815. nagahara
  7816. nagahara
  7817. kametani
  7818. nagai
  7819. nagai
  7820. nagai
  7821. hamaguchi
  7822. nagao
  7823. nagao
  7824. nagata
  7825. nagata
  7826. saito
  7827. nagata
  7828. nagata
  7829. nagel
  7830. nagel
  7831. nagubandi
  7832. naidu
  7833. naidu
  7834. naito
  7835. naito
  7836. najera
  7837. najera
  7838. nakada
  7839. nakagawa
  7840. nakagawa
  7841. nakai
  7842. nakai
  7843. takeshi
  7844. nakamura
  7845. nakamura
  7846. nakamura
  7847. nakamura
  7848. nakamura
  7849. nakanishi
  7850. nakanishi
  7851. nakanishi
  7852. nakasu
  7853. nakasu
  7854. nakata
  7855. nakata
  7856. nakatani
  7857. nakatani
  7858. nakatsuka
  7859. nakatsuka
  7860. nakayama
  7861. nakayama
  7862. konishi
  7863. hoshino
  7864. nakazaki
  7865. nakazaki
  7866. nambiar
  7867. nambiar
  7868. namor
  7869. nangia
  7870. nangia
  7871. nanjundiah
  7872. naomi
  7873. naota
  7874. naota
  7875. takeshi
  7876. naota
  7877. takeshi
  7878. naqvi
  7879. narang
  7880. narasaka
  7881. narasaka
  7882. narasimhan
  7883. narasimhan
  7884. narayana
  7885. narayana
  7886. periasamy
  7887. narayanan
  7888. naresh
  7889. narisawa
  7890. naruse
  7891. naruse
  7892. natale
  7893. natale
  7894. mirzaei
  7895. natale
  7896. nicholas
  7897. natekar
  7898. nayyar
  7899. nayyar
  7900. naresh
  7901. nazarenko
  7902. nazareno
  7903. nazareno
  7904. nazin
  7905. nazin
  7906. manelis
  7907. neale
  7908. neale
  7909. nebois
  7910. nebois
  7911. neckers
  7912. nedelec
  7913. nedogrey
  7914. nedogrey
  7915. syraeva
  7916. kantor
  7917. rakhmankylov
  7918. neeland
  7919. nefedov
  7920. nefedov
  7921. nefedov
  7922. sinotova
  7923. lebedev
  7924. negeshi
  7925. negeshi
  7926. negin
  7927. negishi
  7928. negishi
  7929. negishi
  7930. brown
  7931. negishi
  7932. negishi
  7933. takahashi
  7934. negishi
  7935. idacavage
  7936. negishi
  7937. takahashi
  7938. negishi
  7939. abdalla
  7940. mohamed
  7941. negri
  7942. nelke
  7943. nelson
  7944. nelson
  7945. nemeth
  7946. nemoto
  7947. nemoto
  7948. nesper
  7949. nesper
  7950. nestrick
  7951. nesunts
  7952. neumann
  7953. neumann
  7954. neumann
  7955. hillgaertner
  7956. baines
  7957. dicke
  7958. vorspohl
  7959. neveus
  7960. newbury
  7961. newcomb
  7962. newcomb
  7963. newkome
  7964. newkome
  7965. newkome
  7966. newkome
  7967. moorefield
  7968. baker
  7969. newkome
  7970. paudler
  7971. newkome
  7972. sauer
  7973. roper
  7974. hayer
  7975. newman
  7976. newman
  7977. magerlein
  7978. newton
  7979. newton
  7980. newton
  7981. roberts
  7982. taylor
  7983. ngochindo
  7984. ngochindo
  7985. nicholas
  7986. nicholas
  7987. nicholson
  7988. nicholson
  7989. brian
  7990. nickon
  7991. nickon
  7992. nickson
  7993. nickson
  7994. niclas
  7995. nicolaou
  7996. nicolaou
  7997. nicolaou
  7998. nicolaou
  7999. ogilvie
  8000. nicolaou
  8001. ramphal
  8002. petasis
  8003. serhan
  8004. nicolaou
  8005. smith
  8006. nicolaou
  8007. petasis
  8008. nicolaou
  8009. kyriacos
  8010. costa
  8011. niecke
  8012. niecke
  8013. gudat
  8014. nielsen
  8015. nielsen
  8016. houlihan
  8017. nieman
  8018. nieman
  8019. niestroj
  8020. niestroj
  8021. nifant'ev
  8022. nifant'ev
  8023. grachev
  8024. nifant'ev
  8025. predvoditelev
  8026. niitsuma
  8027. nikitaev
  8028. nikolai
  8029. nikonov
  8030. nikonov
  8031. balyeva
  8032. nilsson
  8033. nilsson
  8034. nimal
  8035. ninomiya
  8036. ninomiya
  8037. ninomiya
  8038. naito
  8039. nishida
  8040. nishida
  8041. nishigaichi
  8042. nishigaichi
  8043. nishigaichi
  8044. takuwa
  8045. naruta
  8046. maruyama
  8047. nishikawa
  8048. nishikawa
  8049. nishimura
  8050. nishimura
  8051. okada
  8052. inokuma
  8053. nakamura
  8054. nishio
  8055. nishio
  8056. hirota
  8057. nishio
  8058. nishio
  8059. nishiyama
  8060. nishiyama
  8061. nishizawa
  8062. nishizawa
  8063. nixon
  8064. nixon
  8065. niyazymbetov
  8066. niyogi
  8067. nobel
  8068. noble
  8069. noboru
  8070. noels
  8071. noels
  8072. graziani
  8073. hubert
  8074. noels
  8075. graziani
  8076. hubert
  8077. nogradi
  8078. nogradi
  8079. nokami
  8080. nokami
  8081. nomura
  8082. nomura
  8083. nomura
  8084. nonhehel
  8085. nonhehel
  8086. norin
  8087. norman
  8088. normant
  8089. normant
  8090. normant
  8091. normant
  8092. normant
  8093. alexakis
  8094. normant
  8095. marek
  8096. lefrancois
  8097. normant
  8098. norrix
  8099. north
  8100. north
  8101. north
  8102. michael
  8103. norton
  8104. norton
  8105. notario
  8106. novak
  8107. novikov
  8108. nowotny
  8109. nowotny
  8110. noyori
  8111. noyori
  8112. hayakawa
  8113. noyori
  8114. kitamura
  8115. noyori
  8116. suzuki
  8117. noyori
  8118. takaya
  8119. nozaki
  8120. nozaki
  8121. nozaki
  8122. nozoe
  8123. nozoe
  8124. noels
  8125. graziani
  8126. hubert
  8127. noyori
  8128. nugent@
  8129. bayer//m
  8130. linkov
  8131. akhrem
  8132. vol'pin
  8133. ogura
  8134. hasegawa
  8135. suami
  8136. ojima
  8137. omura
  8138. orchin
  8139. otera
  8140. ottens
  8141. hildebrandt
  8142. overman
  8143. beak@
  8144. prodger
  8145. panek
  8146. paquette
  8147. paquette
  8148. parvez@
  8149. paterson
  8150. patney
  8151. paulsen
  8152. pedersen
  8153. pelte@
  8154. perlmutter
  8155. petrosyan
  8156. niyazymbetov
  8157. pfaltz
  8158. pirrung
  8159. ponomarev
  8160. porter
  8161. prager
  8162. procter@
  8163. pulham@
  8164. bruckner@
  8165. raifel'd
  8166. vaisman
  8167. randriamahefa@
  8168. samsoniya
  8169. targamadze
  8170. suvorov
  8171. sarkar
  8172. saxton
  8173. scheff
  8174. nugent
  8175. nugent
  8176. nugent
  8177. mayer
  8178. nurrenbach
  8179. nussbeutel
  8180. nutley
  8181. nyberg
  8182. nyerges
  8183. nyerges
  8184. nyiondibonguen
  8185. nyiondibonguen
  8186. nylund
  8187. nylund
  8188. er//m
  8189. linkov
  8190. akhrem
  8191. vol'pin
  8192. linkov
  8193. akhrem
  8194. vol'pin
  8195. yonemitsu
  8196. o'connor
  8197. o'connor
  8198. o'donnell
  8199. o'donnell
  8200. o'donovan
  8201. o'donovan
  8202. o'hagan
  8203. o'hagan
  8204. o'hare
  8205. o'hare
  8206. o'neil
  8207. furukawa
  8208. heathcock
  8209. heathcock
  8210. oberhauser
  8211. oberhauser
  8212. faber
  8213. griengl
  8214. obraztsov
  8215. obrecht
  8216. obrecht
  8217. ochoa
  8218. oediger
  8219. oediger
  8220. moller
  8221. eiter
  8222. oesterle
  8223. ogawa
  8224. ogawa
  8225. ogawa
  8226. akiya
  8227. ogawa
  8228. ogawa
  8229. ogawa
  8230. ogilvie
  8231. ogino
  8232. ogino
  8233. ogino
  8234. ogliaruso
  8235. ogliaruso
  8236. wolfe
  8237. ogura
  8238. ogura
  8239. otsubo
  8240. ogura
  8241. fumio
  8242. ogura
  8243. hasega
  8244. suami
  8245. ogura
  8246. hasegawa
  8247. suami
  8248. ogura
  8249. hasegawa
  8250. suami
  8251. ogura
  8252. reilly
  8253. taeboem
  8254. ohagan
  8255. ohfune
  8256. ohfune
  8257. ohlmeyer
  8258. otsuka
  8259. ohwada
  8260. ohwada
  8261. oikawa
  8262. oikawa
  8263. oishi
  8264. oishi
  8265. oishi
  8266. nakata
  8267. ojima
  8268. ojima
  8269. bastos
  8270. okabe
  8271. okada
  8272. okamoto
  8273. okamoto
  8274. okamoto
  8275. okamura
  8276. okamura
  8277. okamura
  8278. curtin
  8279. okauchi
  8280. okauchi
  8281. okazaki
  8282. okazaki
  8283. renji
  8284. okita
  8285. okitsu
  8286. oksanen
  8287. oksanen
  8288. okubo
  8289. okubo
  8290. masao
  8291. okuda
  8292. okuda
  8293. okuma
  8294. okuma
  8295. olafson
  8296. prakash
  8297. malhotra
  8298. narang
  8299. narang
  8300. prakash
  8301. chambers
  8302. prakash
  8303. sommer
  8304. reddy
  8305. prahsh
  8306. williams
  8307. oldham
  8308. oliveira
  8309. oliver
  8310. oliver
  8311. reiser
  8312. olivero
  8313. oliveros
  8314. olivier
  8315. olivo
  8316. olivucci
  8317. oller
  8318. ollis
  8319. olofson
  8320. olofson
  8321. olsson
  8322. olsson
  8323. olveira-campos
  8324. omura
  8325. kazuya
  8326. oppolzer
  8327. oppolzer
  8328. oppolzer
  8329. oppolzer
  8330. snieckus
  8331. orchin
  8332. orchin
  8333. orena
  8334. organ
  8335. organ
  8336. oriyama
  8337. oriyama
  8338. orjales
  8339. orjales
  8340. orlinkov
  8341. ormiston
  8342. ornstein
  8343. ornstein
  8344. ortiz
  8345. osamu
  8346. osamu
  8347. motoi
  8348. osawa
  8349. osawa
  8350. yonemitsu
  8351. osborn
  8352. osborn
  8353. oshea
  8354. oshea
  8355. donal
  8356. oshima
  8357. oshry
  8358. oshry
  8359. rosenfeld
  8360. osipov
  8361. osipov
  8362. kolomiets
  8363. fokin
  8364. osterberg
  8365. osterberg
  8366. carolyn
  8367. osterhout
  8368. osterhout
  8369. nadler
  8370. padwa
  8371. osterhout
  8372. martin
  8373. ostovic
  8374. ostovic
  8375. bruice
  8376. ostrovskii
  8377. oswald
  8378. otera
  8379. otera
  8380. junzo
  8381. otsubo
  8382. otsubo
  8383. otsuji
  8384. otsuji
  8385. yoshio
  8386. otsuka
  8387. otsuka
  8388. ottens
  8389. ottens
  8390. hildebrandt
  8391. ottens
  8392. hildebrandt
  8393. ottosson
  8394. ovaska
  8395. ovaska
  8396. ovcharenko
  8397. overall
  8398. overberger
  8399. overberger
  8400. sannes
  8401. overman
  8402. overman
  8403. abelman
  8404. kucera
  8405. ricca
  8406. owski
  8407. owsley
  8408. ozaki
  8409. ozaki
  8410. ozawa
  8411. ozawa
  8412. paddon
  8413. paddon
  8414. michael
  8415. paddon-row
  8416. padwa
  8417. padwa
  8418. padwa
  8419. austin
  8420. padwa
  8421. hornbuckle
  8422. padwa
  8423. krumpe
  8424. padwa
  8425. murphree
  8426. padwa
  8427. albert
  8428. paetzold
  8429. paetzold
  8430. paetzold
  8431. grundken
  8432. paganelli
  8433. klair
  8434. rosenthal
  8435. prodger
  8436. pahor
  8437. paknikar
  8438. paknikar
  8439. kirtane
  8440. pakusch
  8441. palacios
  8442. palacios
  8443. paley
  8444. paley
  8445. palkowitz
  8446. palkowitz
  8447. paloma
  8448. paloma
  8449. palomo
  8450. palomo
  8451. palou
  8452. palou
  8453. palyulin
  8454. pancrazi
  8455. pancrazi
  8456. pandey
  8457. pandey
  8458. pandey
  8459. ganesh
  8460. pandiewicz
  8461. pandiewicz
  8462. watanabe
  8463. pandit
  8464. pandit
  8465. pandurangi
  8466. pandurangi
  8467. panek
  8468. panetta
  8469. panetta
  8470. heimer
  8471. hussey
  8472. metzger
  8473. pankowski
  8474. pankowski
  8475. panov
  8476. panunzio
  8477. panza
  8478. papageorgiou
  8479. papamicael
  8480. papamicael
  8481. pappalardo
  8482. pappo
  8483. paquette
  8484. paquette
  8485. paquette
  8486. paquette
  8487. stirling
  8488. parakka
  8489. parakka
  8490. parekh
  8491. parham
  8492. parham
  8493. bradsher
  8494. parish
  8495. parkanyi
  8496. parkanyi
  8497. parker
  8498. parker
  8499. parker
  8500. parmar
  8501. parmar
  8502. prasad
  8503. sharma
  8504. bisht
  8505. sinha
  8506. taneja
  8507. parmerter
  8508. parmerter
  8509. parmon
  8510. parnes
  8511. parnes
  8512. bolestova
  8513. parshall
  8514. parshall
  8515. ittel
  8516. parshall
  8517. nugent
  8518. parshall
  8519. nugent
  8520. parsons
  8521. parsons
  8522. parsons
  8523. parsons
  8524. passmore
  8525. parsons
  8526. simon
  8527. parvez
  8528. parvez
  8529. pashkevich
  8530. pasquato
  8531. passmore
  8532. passmore
  8533. pasto
  8534. pasto
  8535. pasto
  8536. taylor
  8537. pastor
  8538. patai
  8539. patai
  8540. patai
  8541. rappoport
  8542. patai
  8543. rappoport
  8544. stirling
  8545. patai
  8546. patane
  8547. patel
  8548. paterson
  8549. paterson
  8550. berrisford
  8551. paterson
  8552. mansuri
  8553. patil
  8554. patil
  8555. patney
  8556. patney
  8557. patney
  8558. paton
  8559. paton
  8560. patonay
  8561. patonay
  8562. patra
  8563. patra
  8564. patricia
  8565. pattenden
  8566. pattenden
  8567. patterson
  8568. patterson
  8569. patterson
  8570. patwardhan
  8571. patwardhan
  8572. paudler
  8573. o'neil
  8574. pauling
  8575. paulini
  8576. paulini
  8577. paulmier
  8578. paulmier
  8579. paulsen
  8580. pausler
  8581. pausler
  8582. paust
  8583. paust
  8584. pavlenko
  8585. pavlenko
  8586. pavlik
  8587. pawlak
  8588. payne
  8589. pearce
  8590. pearce
  8591. wulfman
  8592. pearson
  8593. pearson
  8594. pearson
  8595. buehler
  8596. pearson
  8597. pearson
  8598. pebrenko
  8599. pedersen
  8600. pedersen
  8601. pedersen
  8602. pederson
  8603. pederson
  8604. pedregal
  8605. pedregal
  8606. pedrocchi
  8607. letourneau
  8608. pelcman
  8609. pelikan
  8610. pelizzi
  8611. pellacani
  8612. pellissier
  8613. pellissier
  8614. pelter
  8615. pelter
  8616. smith
  8617. brown
  8618. pelter
  8619. smith
  8620. jones
  8621. pelter
  8622. andrew
  8623. pelyvas
  8624. pelyvas
  8625. monneret
  8626. herczegh
  8627. penner-hahn
  8628. penner-hahn
  8629. penning
  8630. penzlin
  8631. pepito
  8632. pepito
  8633. peralez
  8634. peralez
  8635. perchec
  8636. pereira
  8637. pereira
  8638. srebnik
  8639. perekalin
  8640. peres
  8641. peresypkina
  8642. pereyre
  8643. pereyre
  8644. quintard
  8645. perez
  8646. perez
  8647. perez
  8648. perezperez
  8649. perezperez
  8650. pergamon
  8651. periasamy
  8652. perichon
  8653. perie
  8654. perkins
  8655. perkins
  8656. berti
  8657. brooks
  8658. grierson
  8659. grimes
  8660. jenkins
  8661. perlmutter
  8662. perlmutter
  8663. perlmutter
  8664. perlmutter
  8665. perrin
  8666. perrin
  8667. perrocheau
  8668. perrocheau
  8669. perron
  8670. perron
  8671. albizati
  8672. perrone
  8673. persoons
  8674. persoons
  8675. perst
  8676. perst
  8677. perutz
  8678. perutz
  8679. perutz
  8680. mccamley
  8681. whittlesey
  8682. perutz
  8683. robin
  8684. petasis
  8685. petasis
  8686. petasis
  8687. patane
  8688. peter
  8689. peter
  8690. peter
  8691. peter
  8692. stephenson
  8693. peters
  8694. petersen
  8695. petersen
  8696. peterson
  8697. peterson
  8698. peterson
  8699. petit
  8700. petit
  8701. petitou
  8702. petitou
  8703. boeckel
  8704. petragnani
  8705. petragnani
  8706. petragnani
  8707. comasseto
  8708. petragnani
  8709. ferraz
  8710. silva
  8711. petragnani
  8712. yonashiro
  8713. petre
  8714. petre
  8715. petrini
  8716. petrini
  8717. petrosyan
  8718. petrosyan
  8719. niyazymbetov
  8720. petrov
  8721. petrov
  8722. rudnev
  8723. sorokin
  8724. petrova
  8725. petrova
  8726. petrovich
  8727. petrzilka
  8728. petrzilka
  8729. grayson
  8730. pettit
  8731. pettit
  8732. pettit
  8733. tamelen
  8734. petty
  8735. peyman
  8736. armor
  8737. pfaff
  8738. pfaltz
  8739. pfander
  8740. pfander
  8741. pfander
  8742. stoll
  8743. pfeffer
  8744. pfeffer
  8745. pfenniger
  8746. pfenniger
  8747. pfleiderer
  8748. pfleiderer
  8749. pfleiderer
  8750. gottlieb
  8751. phadke
  8752. philip
  8753. philip
  8754. roussel
  8755. philip
  8756. magnus
  8757. philippe
  8758. philips
  8759. philips
  8760. phillips
  8761. philp
  8762. philp
  8763. stoddart
  8764. piancatelli
  8765. piancatelli
  8766. piancatelli
  8767. dauria
  8768. donofrio
  8769. piancatelli
  8770. scettri
  8771. d'auria
  8772. picard
  8773. picard
  8774. piccirilli
  8775. pierce
  8776. pierce
  8777. piere
  8778. pierre
  8779. piers
  8780. piers
  8781. piers
  8782. shapiro
  8783. bunel
  8784. bercaw
  8785. pietek
  8786. pietra
  8787. pietrusiewicz
  8788. pietrusiewicz
  8789. zablocka
  8790. piettre
  8791. sweigart
  8792. sobinski
  8793. mcmanus
  8794. pikul
  8795. pillai
  8796. pilling
  8797. pilling
  8798. pinder
  8799. pinder
  8800. pindur
  8801. pindur
  8802. pindur
  8803. erfanian-abdoust
  8804. pindur
  8805. pindur
  8806. muller
  8807. witzel
  8808. pindur
  8809. schneider
  8810. pines
  8811. pines
  8812. pinhey
  8813. pinhey
  8814. pinnick
  8815. pinnick
  8816. pinsker
  8817. piotr
  8818. piotti
  8819. piotti
  8820. piozzi
  8821. piozzi
  8822. franco
  8823. pirkle
  8824. pirkle
  8825. pochapsky
  8826. pirozhkov
  8827. pirrung
  8828. pirrung
  8829. pirrung
  8830. pisulina
  8831. pisulina
  8832. pizzo
  8833. pizzotti
  8834. pizzotti
  8835. platanov
  8836. platanov
  8837. yakobson
  8838. platz
  8839. platz
  8840. platz
  8841. platz
  8842. matthew
  8843. pleixats
  8844. pleixats
  8845. roser
  8846. pleixatz
  8847. plesek
  8848. plesek
  8849. plesek
  8850. hermanek
  8851. stibr
  8852. pletcher
  8853. pletcher
  8854. ploegh
  8855. plueddemann
  8856. plueddemann
  8857. pochapsky
  8858. podraza
  8859. podraza
  8860. pohlmann
  8861. poirier
  8862. poirier
  8863. poitras
  8864. poitras
  8865. polimbetova
  8866. polimbetova
  8867. polivin
  8868. polivin
  8869. karakhanov
  8870. postnov
  8871. pollack
  8872. pollack
  8873. pollard
  8874. pollard
  8875. poller
  8876. poller
  8877. poloni
  8878. pomme
  8879. pomme
  8880. thieme
  8881. pommer
  8882. pommer
  8883. pommer
  8884. nurrenbach
  8885. pommier
  8886. pommier
  8887. ponec
  8888. ponec
  8889. ponomarev
  8890. ponomarev
  8891. santelli
  8892. popandovayambolieva
  8893. popandovayambolieva
  8894. mueller
  8895. popkov
  8896. poppe
  8897. poppe
  8898. novak
  8899. pornet
  8900. pornet
  8901. porshnev
  8902. porter
  8903. porter
  8904. porter
  8905. porter
  8906. giese
  8907. curran
  8908. porter
  8909. krebs
  8910. posner
  8911. posner
  8912. pospichal
  8913. pospisil
  8914. pospisil
  8915. klemchuk
  8916. schreiber
  8917. christopher
  8918. postema
  8919. postema
  8920. postnov
  8921. potier
  8922. potin
  8923. potin
  8924. potkin
  8925. pottlloff
  8926. potts
  8927. potts
  8928. bauer
  8929. pourreau
  8930. pourreau
  8931. geoffroy
  8932. poveda
  8933. power
  8934. power
  8935. pozharskii
  8936. prager
  8937. prager
  8938. prager
  8939. prahsh
  8940. prajapati
  8941. prajapati
  8942. prakash
  8943. prakash
  8944. prakash
  8945. saini
  8946. sharma
  8947. prakash
  8948. singh
  8949. prakash
  8950. prasad
  8951. prasanna
  8952. pratt
  8953. pratt
  8954. pratt
  8955. predvoditelev
  8956. prein
  8957. prein
  8958. prelog
  8959. premuzic
  8960. press
  8961. preston
  8962. prestwich
  8963. price
  8964. price
  8965. price
  8966. iddon
  8967. wakefield
  8968. price
  8969. silva
  8970. cavaleiro
  8971. price
  8972. william
  8973. priess
  8974. prilezhaeva
  8975. primke
  8976. primke
  8977. prinzbach
  8978. prinzbach
  8979. weber
  8980. prodger
  8981. pross
  8982. pross
  8983. pross
  8984. shaik
  8985. protasiewicz
  8986. protopopova
  8987. protopopova
  8988. shapiro
  8989. proudhan
  8990. proudhan
  8991. przemyslaw
  8992. pudova
  8993. pudovik
  8994. pudovik
  8995. konovalova
  8996. pujari
  8997. pujari
  8998. pulham
  8999. purdy
  9000. putala
  9001. putala
  9002. lemenovskii
  9003. quallich
  9004. quallich
  9005. quaranta
  9006. quaranta
  9007. tommasi
  9008. quayle
  9009. quayle
  9010. queguiner
  9011. queguiner
  9012. marsais
  9013. snieckus
  9014. epsztajn
  9015. queneau
  9016. quentin
  9017. quesnelle
  9018. quesnelle
  9019. quinou
  9020. quinou
  9021. guilloton
  9022. quintana
  9023. quintana
  9024. delia
  9025. quintard
  9026. quintero
  9027. raban
  9028. rabidea
  9029. rabidea
  9030. marcinow
  9031. rabideau
  9032. rabideau
  9033. rabinovitz
  9034. rabinovitz
  9035. rabinovitz
  9036. cohen
  9037. rabjohn
  9038. rabjohn
  9039. racherla
  9040. racherla
  9041. rachita
  9042. rachwal
  9043. radchenko
  9044. radchenko
  9045. petrov
  9046. bouzard
  9047. raevskii
  9048. raevskii
  9049. raffaelli
  9050. ragnarsson
  9051. ragnarsson
  9052. grehn
  9053. rahman
  9054. rahman
  9055. rahul
  9056. rahul
  9057. vohra
  9058. rai-shung
  9059. rai-shung
  9060. raifel'd
  9061. raifel'd
  9062. vaisman
  9063. rainer
  9064. rainina
  9065. rajakumar
  9066. rajakumar
  9067. rajanbabu
  9068. rajanbabu
  9069. rajappa
  9070. rajappa
  9071. rajappa
  9072. natekar
  9073. rajca
  9074. rajca
  9075. rajeswaru
  9076. rajeswaru
  9077. chandrasekharam
  9078. govindachari
  9079. rajopadhye
  9080. rajopadhye
  9081. rajzmann
  9082. rakhmankylov
  9083. rakhmatulina
  9084. ramachandran
  9085. ramadan
  9086. ramadas
  9087. ramadas
  9088. srinivasan
  9089. ramachandran
  9090. sastri
  9091. ramaiah
  9092. ramaiah
  9093. ramamurthy
  9094. ramamurthy
  9095. ramamurthy
  9096. weiss
  9097. hammond
  9098. raman
  9099. raman
  9100. ramana
  9101. ramirez
  9102. ramirez
  9103. ramirez
  9104. marecek
  9105. ramos
  9106. ramos
  9107. bellus
  9108. ramphal
  9109. ramsden
  9110. ramsden
  9111. randaccio
  9112. randaccio
  9113. pahor
  9114. zangrando
  9115. marzilli
  9116. randic
  9117. randic
  9118. rando
  9119. rando
  9120. randriamahefa
  9121. randriamahefa
  9122. raner
  9123. ranganathan
  9124. ranganathan
  9125. ranganathan
  9126. mehrotra
  9127. brindaban
  9128. rapoport
  9129. rapoport
  9130. raposo
  9131. raposo
  9132. rappa
  9133. rappoport
  9134. rappoport
  9135. rappoport
  9136. rappoprt
  9137. rappoprt
  9138. rasala
  9139. raschke
  9140. rashed
  9141. rasmussen
  9142. rasmussen
  9143. rasmussen
  9144. hassner
  9145. rastelli
  9146. rastogi
  9147. rastogi
  9148. sharma
  9149. raston
  9150. ratavelomanana
  9151. ratcliffe
  9152. rathke
  9153. rathke
  9154. ratnam
  9155. ratovelomanana
  9156. ratovelomanana
  9157. ratovskii
  9158. ratovskii
  9159. raubenheimer
  9160. raubo
  9161. raubo
  9162. rauchschwalbe
  9163. raulins
  9164. ravikumar
  9165. ravikumar
  9166. ravindranathan
  9167. rawal
  9168. rawal
  9169. rawson
  9170. raymond
  9171. rayner
  9172. rayner
  9173. raynolds
  9174. reary
  9175. reary
  9176. rebek
  9177. rebek
  9178. rebek
  9179. rebiere
  9180. reddy
  9181. reddy
  9182. redlich
  9183. redlich
  9184. reese
  9185. reese
  9186. reetz
  9187. reetz
  9188. reeve
  9189. reeve
  9190. reger
  9191. reger
  9192. reginato
  9193. regitz
  9194. regitz
  9195. regitz
  9196. regitz
  9197. giese
  9198. regitz
  9199. regitz
  9200. manfred
  9201. reich
  9202. reich
  9203. reich
  9204. wollowitz
  9205. reichardt
  9206. reichardt
  9207. reidel
  9208. reider
  9209. reilly
  9210. reilly
  9211. michael
  9212. reimlinger
  9213. reinecke
  9214. reinecke
  9215. reinhardt
  9216. reinhardt
  9217. reinhold
  9218. reinhoudt
  9219. reinhoudt
  9220. reinhoudt
  9221. david
  9222. reinmuth
  9223. reiser
  9224. reiser
  9225. reiser
  9226. olivier
  9227. reissig
  9228. reissig
  9229. reissig
  9230. reitz
  9231. remers
  9232. remers
  9233. renaud
  9234. renaud
  9235. renji
  9236. resek
  9237. reshetova
  9238. reshetova
  9239. tkhap
  9240. kamernitskii
  9241. resnati
  9242. resnati
  9243. resnati
  9244. ressig
  9245. retey
  9246. retey
  9247. retherford
  9248. rethwisch
  9249. rettig
  9250. rettig
  9251. rettig
  9252. wolfgang
  9253. reucroft
  9254. reucroft
  9255. sammes
  9256. reuman
  9257. reuman
  9258. meyers
  9259. reutov
  9260. reutov
  9261. reutrakul
  9262. reutrakul
  9263. rewcastle
  9264. rewcastle
  9265. rewcatle
  9266. rewcatle
  9267. katritzky
  9268. reznikov
  9269. rheingold
  9270. rhoads
  9271. rhoads
  9272. raulins
  9273. rhode
  9274. rhode
  9275. negin
  9276. abdou
  9277. daboun
  9278. riant
  9279. riant
  9280. ricca
  9281. ricci
  9282. ricci
  9283. degl'innocenti
  9284. ricci
  9285. reginato
  9286. degl'innocenti
  9287. seconi
  9288. riccio
  9289. richmond
  9290. thomas
  9291. richter
  9292. richter
  9293. richter
  9294. markus
  9295. rickborn
  9296. riddell
  9297. riddell
  9298. riediker
  9299. rieke
  9300. rieke
  9301. boucherle
  9302. clousse
  9303. mouzin
  9304. rigby
  9305. rigby
  9306. righi
  9307. rimoldi
  9308. rinehart
  9309. ripoll
  9310. ripoll
  9311. vallee
  9312. ritter
  9313. ritter
  9314. ritter
  9315. rivera
  9316. rivera
  9317. rivett
  9318. rizzi
  9319. robert
  9320. roberts
  9321. roberts
  9322. roberts
  9323. williams
  9324. roberts
  9325. sharts
  9326. roberts
  9327. roberts
  9328. wiggins
  9329. robertson
  9330. robertson
  9331. robin
  9332. robins
  9333. robins
  9334. robins
  9335. richard
  9336. robinson
  9337. robinson
  9338. rochet
  9339. rochet
  9340. rockett
  9341. rockett
  9342. rodin
  9343. rodionov
  9344. rodionov
  9345. furin
  9346. rodney
  9347. rodrigo
  9348. rodrigo
  9349. rodrigues
  9350. rodrigues
  9351. rodriguez
  9352. rodriguez
  9353. rodriguez
  9354. dulcere
  9355. rodriguez
  9356. rodriguez
  9357. roelens
  9358. roelens
  9359. roesky
  9360. roesky
  9361. roganov
  9362. rogers
  9363. rogic
  9364. rogic
  9365. rohmer
  9366. rokach
  9367. rokach
  9368. rokach
  9369. adams
  9370. rokhlin
  9371. rokita
  9372. rolfs
  9373. rolfs
  9374. romanenko
  9375. romanov
  9376. romanov
  9377. romanova
  9378. romeo
  9379. romeo
  9380. romer
  9381. romer
  9382. romers
  9383. romers
  9384. altona
  9385. havinga
  9386. romine
  9387. romney-alexander
  9388. romney-alexander
  9389. meyers
  9390. romine
  9391. midura
  9392. meyers
  9393. romsey-alexander
  9394. rondsetvedt
  9395. rondsetvedt
  9396. ronne
  9397. ronne
  9398. roper
  9399. harvey
  9400. arnett
  9401. rosen
  9402. rosen
  9403. heathcock
  9404. rosen
  9405. nagel
  9406. rizzi
  9407. rosenblum
  9408. rosenblum
  9409. rosenblum
  9410. bucheister
  9411. chang
  9412. cohen
  9413. marsi
  9414. samuels
  9415. rosenfeld
  9416. rosenthal
  9417. roser
  9418. ballini
  9419. petrini
  9420. marotta
  9421. righi
  9422. rosin
  9423. rosin
  9424. franzini
  9425. raffaelli
  9426. salvadori
  9427. rosini
  9428. rosini
  9429. rosini
  9430. balleni
  9431. roskamp
  9432. roskamp
  9433. rosling
  9434. rosling
  9435. rossa
  9436. rossa
  9437. vogtle
  9438. rossiC
  9439. rossi
  9440. rossi
  9441. diversi
  9442. rossi
  9443. rossi
  9444. rossi
  9445. palacios
  9446. rossi
  9447. rossiter
  9448. rossiter
  9449. swingle
  9450. rotella
  9451. rothe
  9452. rotstein
  9453. rouillard
  9454. roundhill
  9455. roundhill
  9456. roush
  9457. roush
  9458. roussel
  9459. rowlinson
  9460. rowlinson
  9461. sosnovsky
  9462. roxburgh
  9463. roxburgh
  9464. rozanov
  9465. rozants
  9466. rozants
  9467. sholle
  9468. rozema
  9469. rozen
  9470. rozen
  9471. rozen
  9472. filler
  9473. rozovskii
  9474. rozovskii
  9475. rozwadowska
  9476. rozwadowska
  9477. rstner
  9478. ruane
  9479. ruane
  9480. wilson
  9481. ruano
  9482. ruasse
  9483. ruasse
  9484. ruasse
  9485. motallebi
  9486. rubin
  9487. rubin
  9488. rubinstein
  9489. rubinstein
  9490. ruchardt
  9491. ruchardt
  9492. ruchardt
  9493. beckhaus
  9494. ruchardt
  9495. meier
  9496. pakusch
  9497. wolber
  9498. muller
  9499. rudchenko
  9500. rudchenko
  9501. rudiger
  9502. rudler
  9503. rudler
  9504. audouin
  9505. chelain
  9506. denise
  9507. goumont
  9508. rudnev
  9509. rudolf
  9510. rudorf
  9511. rudorf
  9512. rudorf
  9513. schwarz
  9514. ruffing
  9515. ruffing
  9516. ruffolo
  9517. ruffolo
  9518. ruiz-lopez
  9519. ruppin
  9520. rusanov
  9521. rusanov
  9522. rusch
  9523. russell
  9524. russell
  9525. rutledge
  9526. ruveda
  9527. ruzziconi
  9528. ruzziconi
  9529. ryabov
  9530. ryabov
  9531. ryakhovskii
  9532. ryakhovskii
  9533. agafonov
  9534. kosyrev
  9535. ryang
  9536. ryang
  9537. tsutsumi
  9538. ryashentseva
  9539. ryashentseva
  9540. maragarita
  9541. rybakova
  9542. rybakova
  9543. prilezhaeva
  9544. litvinov
  9545. rychly
  9546. rychly
  9547. klimo
  9548. pelikan
  9549. valko
  9550. rychnovsky
  9551. rychnovsky
  9552. skrabal
  9553. zollinger
  9554. rytina
  9555. denmark
  9556. martin
  9557. bertz
  9558. heffold
  9559. inoki
  9560. danishefsky
  9561. buchwald
  9562. schreiber
  9563. danishefsky
  9564. murai
  9565. tanis
  9566. samaritani
  9567. saberi
  9568. sadek
  9569. sadek
  9570. kamal
  9571. sadekov
  9572. sadekov
  9573. maksimenko
  9574. minkin
  9575. sadova
  9576. sadova
  9577. khaikin
  9578. vilkov
  9579. sadowski
  9580. sadowski
  9581. gasteiger
  9582. saengchantara
  9583. saengchantara
  9584. wallace
  9585. saeva
  9586. saeva
  9587. sagitullin
  9588. sahyun
  9589. saigo
  9590. saigo
  9591. saikia
  9592. saikia
  9593. saini
  9594. saini
  9595. sharma
  9596. sainsbury
  9597. sainsbury
  9598. saito
  9599. saito
  9600. saito
  9601. sakai
  9602. sakai
  9603. sakai
  9604. suemune
  9605. sakamoto
  9606. sakamoto
  9607. kondo
  9608. yamanaka
  9609. sakata
  9610. sakata
  9611. makino
  9612. kurasawa
  9613. sakuraba
  9614. sakuraba
  9615. sakuraba
  9616. sakuragi
  9617. sakuragi
  9618. sakurai
  9619. sakurai
  9620. sakurai
  9621. salas
  9622. salaun
  9623. salaun
  9624. salaun
  9625. salazar
  9626. salazar
  9627. salomon
  9628. salomon
  9629. salomon
  9630. salter
  9631. salter
  9632. salvadori
  9633. salvadori
  9634. rosini
  9635. bertucci
  9636. uccello-barretta
  9637. salzer
  9638. saman
  9639. saman
  9640. samankumara
  9641. samarai
  9642. samarai
  9643. samari
  9644. samaritani
  9645. sames
  9646. sames
  9647. samizu
  9648. samizu
  9649. sammakia
  9650. sammakia
  9651. sammes
  9652. sammes
  9653. sammes
  9654. yahioglu
  9655. sammmakia
  9656. samodurova
  9657. samsoniya
  9658. samsoniya
  9659. targamadze
  9660. suvorov
  9661. samuel
  9662. samuels
  9663. sandanayake
  9664. sandanayake
  9665. samankumara
  9666. sander
  9667. sander
  9668. sander
  9669. bucher
  9670. sanders
  9671. sandhu
  9672. sandhu
  9673. sandler
  9674. sandler
  9675. sanford
  9676. sanjayan
  9677. sanjayan
  9678. sankaran
  9679. sanner
  9680. sannes
  9681. sannigrahi
  9682. sannigrahi
  9683. niyogi
  9684. hobza
  9685. schleyer
  9686. santaniello
  9687. santaniello
  9688. ferraboschi
  9689. grisenti
  9690. manzocchi
  9691. santelli
  9692. santelli-rouvier
  9693. santelli-rouvier
  9694. santelli
  9695. santhosh
  9696. santhosh
  9697. santiago
  9698. santiago
  9699. santoyo-gonzalez
  9700. santoyo-gonzalez
  9701. hernandez-mateo
  9702. santoyogonzalez
  9703. santoyogonzalez
  9704. sappa
  9705. sappa
  9706. tiripicchio
  9707. saraf
  9708. saraf
  9709. al-omran
  9710. al-saleh
  9711. sarel
  9712. sarel
  9713. sarkar
  9714. sarkar
  9715. sarkar
  9716. sarlo
  9717. sarobe
  9718. sarobe
  9719. sasaki
  9720. sasaki
  9721. sasaki
  9722. sasaki
  9723. sastri
  9724. satchell
  9725. satchell
  9726. satchell
  9727. satchell
  9728. satge
  9729. kobayashi
  9730. satoh
  9731. satoh
  9732. satoh
  9733. yamakawa
  9734. sattur
  9735. satyanarayana
  9736. sauer
  9737. saunders
  9738. saunders
  9739. jimenez-vazquez
  9740. saunders
  9741. sausins
  9742. sausins
  9743. duburs
  9744. sauvage
  9745. sauvage
  9746. saveant
  9747. saveant
  9748. sawada
  9749. sawada
  9750. sawamura
  9751. sawamura
  9752. sawamura
  9753. sawyer
  9754. sawyer
  9755. gibson
  9756. saxena
  9757. saxena
  9758. hosmane
  9759. saxton
  9760. saxton
  9761. saxton
  9762. sayed
  9763. scaiano
  9764. scaiano
  9765. scettri
  9766. schacht
  9767. schaefer
  9768. schaefer
  9769. bloomfield
  9770. schafer
  9771. schafer
  9772. schank
  9773. schank
  9774. schantl
  9775. schantl
  9776. scharf
  9777. scharf
  9778. schatz
  9779. schatz
  9780. schaumann
  9781. schaumann
  9782. schaverien
  9783. schaverien
  9784. scheck
  9785. scheeren
  9786. scheern
  9787. scheff
  9788. scheff
  9789. scheff
  9790. scheffer
  9791. scheffold
  9792. scheffold
  9793. schellenberger
  9794. schellenberger
  9795. jakubke
  9796. schemenaur
  9797. schemenaur
  9798. scherer
  9799. scherer
  9800. scheuer
  9801. scheuer
  9802. schick
  9803. schick
  9804. schick
  9805. eichorn
  9806. schiess
  9807. schiessl
  9808. schiessl
  9809. schilbach
  9810. schilbach
  9811. schinzer
  9812. schinzer
  9813. schioett
  9814. schionato
  9815. schlegel
  9816. schlegel
  9817. schlessinger
  9818. schlessinger
  9819. schleyer
  9820. schlosser
  9821. schlosser
  9822. desponds
  9823. lehmann
  9824. moret
  9825. rauchschwalbe
  9826. schlosser
  9827. desponds
  9828. lehmann
  9829. moret
  9830. rauchschwalbe
  9831. schmalz
  9832. schmalz
  9833. schmalz
  9834. schmalz
  9835. gunther
  9836. schmehl
  9837. schmidbaur
  9838. schmidbaur
  9839. schmidpeter
  9840. schmidt
  9841. schmidt
  9842. schmidt
  9843. kinzy
  9844. schmittel
  9845. schmittel
  9846. schmittel
  9847. michael
  9848. schmitz
  9849. schmitz
  9850. schnapp
  9851. schnatter
  9852. schnatter
  9853. wayne
  9854. schneider
  9855. schneider
  9856. schneider
  9857. schneider
  9858. schneller
  9859. schnur
  9860. schnur
  9861. schoemaker
  9862. schoemaker
  9863. boestern
  9864. kaptein
  9865. hermes
  9866. sonke
  9867. schollkopf
  9868. schollkopf
  9869. schreiber
  9870. schreiber
  9871. schreiber
  9872. albers
  9873. rosen
  9874. standaert
  9875. wandl
  9876. schreiber
  9877. verdine
  9878. schlosser
  9879. desponds
  9880. lehmann
  9881. moret
  9882. rauchschwalbe
  9883. schreiber
  9884. stuart
  9885. schultz
  9886. schwemlein@
  9887. seebach
  9888. seerden@
  9889. sessler
  9890. hemmi
  9891. murai
  9892. burrell
  9893. young
  9894. sharpless@
  9895. shibasaki
  9896. shibata
  9897. ikuya@
  9898. shono
  9899. simon
  9900. sinou
  9901. skrabal@
  9902. smith
  9903. sneeden
  9904. snyder
  9905. spangler
  9906. srebnik
  9907. stanek@
  9908. sternbach
  9909. strazzolini
  9910. giumanini
  9911. cauci
  9912. suk-ku
  9913. sullivan@
  9914. suvorov@
  9915. suzuki
  9916. cohen@
  9917. taber
  9918. takai
  9919. takemura@
  9920. tanner
  9921. thurston
  9922. toke@
  9923. tonellato
  9924. toshima
  9925. tatsuta
  9926. trahanovsky
  9927. trost
  9928. trost
  9929. trost
  9930. fleming
  9931. tsoungas
  9932. tsuji
  9933. tyler
  9934. robert
  9935. schreiber
  9936. stuart
  9937. schrock
  9938. schrock
  9939. schroder
  9940. schroder
  9941. schubert
  9942. schubert
  9943. schubert
  9944. ulrich
  9945. schudde
  9946. schuetz
  9947. schuetz
  9948. schulenberg
  9949. schulenberg
  9950. archer
  9951. schulte
  9952. schulte
  9953. schultz
  9954. schultz
  9955. lerner
  9956. schulz
  9957. schulz
  9958. schumann
  9959. schumann
  9960. schummer
  9961. schummer
  9962. schurig
  9963. schurig
  9964. betschinger
  9965. schurig
  9966. nowotny
  9967. schuster
  9968. schuster
  9969. kaprinidis
  9970. schuster
  9971. schuster
  9972. schuster
  9973. coppola
  9974. schwab
  9975. schwab
  9976. henderson
  9977. schwark
  9978. schwartz
  9979. schwartz
  9980. arvanitis
  9981. smegel
  9982. meier
  9983. clift
  9984. schwartz
  9985. labinger
  9986. schwarz
  9987. schwarz
  9988. schweizer
  9989. schweizer
  9990. schwemlein
  9991. schwing-weill
  9992. schwochau
  9993. schwochau
  9994. scialdone
  9995. scialdone
  9996. scobie
  9997. scobie
  9998. scola
  9999. scolastico
  10000. scolastico
  10001. scott
  10002. scott
  10003. scott
  10004. scott
  10005. scott
  10006. scott
  10007. mcmurry
  10008. screttas
  10009. screttas
  10010. steele
  10011. scrimin
  10012. scrimin
  10013. tecilla
  10014. tonellato
  10015. scriven
  10016. scriven
  10017. turnbull
  10018. scriven
  10019. scully
  10020. scully
  10021. searle
  10022. sebald
  10023. sebastian
  10024. sebek
  10025. seconi
  10026. seconi
  10027. sedrani
  10028. seebach
  10029. seebach
  10030. enders
  10031. seebach
  10032. prelog
  10033. vogtle
  10034. seeman
  10035. seeman
  10036. seemayer
  10037. seerden
  10038. seerden
  10039. segnitz
  10040. segnitz
  10041. segundo
  10042. segundo
  10043. seiichi
  10044. seikaly
  10045. seikaly
  10046. tidwell
  10047. seitz
  10048. seitz
  10049. imming
  10050. selva
  10051. selva
  10052. selvaraj
  10053. semikolenov
  10054. semikolenov
  10055. semmelhack
  10056. semmelhack
  10057. semmelhack
  10058. semmelhack
  10059. zhang
  10060. bodurow
  10061. sanner
  10062. dobler
  10063. sengupta
  10064. sengupta
  10065. seniz
  10066. senning
  10067. senning
  10068. seoane
  10069. seppelt
  10070. seppelt
  10071. serebryakov
  10072. serebryakov
  10073. mavrov
  10074. seredkina
  10075. serhan
  10076. serratosa
  10077. serratosa
  10078. servi
  10079. servi
  10080. sessler
  10081. sessler
  10082. burrell
  10083. sessler
  10084. hemmi
  10085. murai
  10086. burrell
  10087. young
  10088. sessler
  10089. jonathan
  10090. sestanj
  10091. sethna
  10092. sethna
  10093. phadke
  10094. sevin
  10095. sevin
  10096. sexsmith
  10097. seyden-penne
  10098. seyden-penne
  10099. seyferth
  10100. seyferth
  10101. shaban
  10102. shaban
  10103. shaban
  10104. sharshira
  10105. shafii
  10106. shafiq
  10107. shafiq
  10108. shafran
  10109. shafran
  10110. bakulev
  10111. mokrushin
  10112. shaik
  10113. shambayati
  10114. shambayati
  10115. shambayati
  10116. crowe
  10117. schreiber
  10118. shamsevaleev
  10119. shang
  10120. shang
  10121. shankar
  10122. shankar
  10123. shannon
  10124. shapakin
  10125. shapiro
  10126. shapiro
  10127. shapiro
  10128. dyatkin
  10129. nefedov
  10130. shapiro
  10131. shapiro
  10132. shapiro
  10133. sharma
  10134. sharma
  10135. sharma
  10136. sharma
  10137. sharpless
  10138. sharpless
  10139. sharpless
  10140. verhoeven
  10141. sharshira
  10142. sharts
  10143. shatenshtein
  10144. shawali
  10145. shawali
  10146. shcherbakova
  10147. sheehan
  10148. sheehan
  10149. corey
  10150. sheikh
  10151. sheldon
  10152. sheldon
  10153. sheldon
  10154. sheldon
  10155. kochi
  10156. sheldrake
  10157. shepherd
  10158. shepherd
  10159. sheppard
  10160. sheppard
  10161. sheppard
  10162. sheridan
  10163. sheringham
  10164. sherrington
  10165. sherrington
  10166. hodge
  10167. shibasaki
  10168. shibata
  10169. shibata
  10170. shibata
  10171. ikuya
  10172. shibata
  10173. shibuya
  10174. shida
  10175. shida
  10176. naomi
  10177. shida
  10178. haselba
  10179. bally
  10180. shigetoshi
  10181. shigetoshi
  10182. takahashi
  10183. shiina
  10184. shiina
  10185. shilov
  10186. shilov
  10187. shilov
  10188. shul'pin
  10189. shilova
  10190. shimamoto
  10191. shimamoto
  10192. shimano
  10193. shimano
  10194. shimizu
  10195. shimizu
  10196. shimizu
  10197. masaki
  10198. shine
  10199. shine
  10200. shing
  10201. shing
  10202. shinkai
  10203. shinkai
  10204. shinkai
  10205. shinokubo
  10206. shinokubo
  10207. shioiri
  10208. shioiri
  10209. shiori
  10210. shiori
  10211. hamada
  10212. shipchandler
  10213. shipchandler
  10214. shirakawa
  10215. shirakawa
  10216. shirley
  10217. shirley
  10218. shiroshita
  10219. shishkina
  10220. shishkina
  10221. berezhnaya
  10222. shnitko
  10223. shoig
  10224. shoji
  10225. shoji
  10226. kajigaeshi
  10227. shokol
  10228. sholle
  10229. shono
  10230. shono
  10231. shono
  10232. shook
  10233. shook
  10234. shore
  10235. shore
  10236. shralel
  10237. shriner
  10238. shriner
  10239. shtefan
  10240. shul'pin
  10241. shultz
  10242. sibille
  10243. sicher
  10244. sicher
  10245. siddhanta
  10246. sidler
  10247. sieber
  10248. sieburth
  10249. sieburth
  10250. siedle
  10251. siedle
  10252. siedlecka
  10253. siegel
  10254. siegel
  10255. sievers
  10256. sigan
  10257. sikora
  10258. sikora
  10259. macomber
  10260. raausch
  10261. silva
  10262. silva
  10263. artur
  10264. silveira
  10265. silveira
  10266. silvester
  10267. silvester
  10268. simamura
  10269. simamura
  10270. simandi
  10271. simandi
  10272. barna
  10273. szeverenyi
  10274. nemeth
  10275. simkin
  10276. simkin
  10277. minkin
  10278. glukhovtsev
  10279. bader
  10280. gunther
  10281. neumann
  10282. thomas
  10283. simmons
  10284. simmons
  10285. cairns
  10286. vladuchick
  10287. hoiness
  10288. simon
  10289. simon
  10290. simon
  10291. simon
  10292. simonet
  10293. simonet
  10294. guillanton
  10295. simoni
  10296. simonoff
  10297. simonova
  10298. simonova
  10299. nefedov
  10300. toropova
  10301. kirillov
  10302. simonyi
  10303. simonyi
  10304. simpkins
  10305. simpkins
  10306. simpson
  10307. simpson
  10308. sinay
  10309. sinay
  10310. sindlerkulyk
  10311. sindlerkulyk
  10312. sinegovskaya
  10313. singaram
  10314. singer
  10315. singh
  10316. singh
  10317. singh
  10318. singh
  10319. singh
  10320. singleton
  10321. sinha
  10322. sinnott
  10323. sinnott
  10324. sinotova
  10325. sinou
  10326. sinyashin
  10327. sinyashin
  10328. batyeva
  10329. pudovik
  10330. siskin
  10331. siskin
  10332. katritzkcy
  10333. sisko
  10334. sizov
  10335. sizov
  10336. kolomiets
  10337. fokin
  10338. skarzewski
  10339. skarzewski
  10340. siedlecka
  10341. skell
  10342. skell
  10343. traynham
  10344. skerlj
  10345. skorobogatova
  10346. skorobogatova
  10347. skrabal
  10348. slack
  10349. slack
  10350. slebocka-tilk
  10351. slivinskii
  10352. slivinskii
  10353. voitsekhovskii
  10354. sliwa
  10355. sliwa
  10356. sliwa
  10357. bachowska
  10358. zelichowicz
  10359. sliwa
  10360. chrzastek
  10361. mielniczak
  10362. sliwa
  10363. mianowska
  10364. sliwa
  10365. wanda
  10366. slough
  10367. smadja
  10368. smadja
  10369. smadja
  10370. william
  10371. smalley
  10372. smallridge
  10373. smeets
  10374. smegel
  10375. smirnov
  10376. caple
  10377. smoliakova
  10378. smith
  10379. smith
  10380. smith
  10381. smith
  10382. smith
  10383. smith
  10384. smith
  10385. smith
  10386. robin
  10387. smithers
  10388. smithrud
  10389. smoliakova
  10390. snapper
  10391. snapper
  10392. sneden
  10393. sneden
  10394. sneeden
  10395. sneeden
  10396. sneeden
  10397. sneen
  10398. sneen
  10399. snider
  10400. snider
  10401. snider
  10402. snider
  10403. barry
  10404. snieckus
  10405. snieckus
  10406. snyder
  10407. yokoyama
  10408. hayasaka
  10409. ebihara
  10410. sobenina
  10411. sobenina
  10412. mikhaleva
  10413. trofimov
  10414. sobinski
  10415. sobolev
  10416. sobti
  10417. sobti
  10418. sodeoka
  10419. sodeoka
  10420. shibasaki
  10421. soderberg
  10422. soderberg
  10423. soderquist
  10424. soderquist
  10425. sogani
  10426. sojka
  10427. sokolov
  10428. sokolov
  10429. stankevich
  10430. sokolovskii
  10431. sokolovskii
  10432. yur'eva
  10433. matros
  10434. sokolyanskaya
  10435. sokolyuk
  10436. sokolyuk
  10437. sokolyuk
  10438. romanov
  10439. pisulina
  10440. solff
  10441. solff
  10442. solladie
  10443. solladie
  10444. solladie-cavallo
  10445. solladie-cavallo
  10446. solodenko
  10447. solodin
  10448. solodin
  10449. soloshonok
  10450. somers
  10451. somfai
  10452. somfai
  10453. sommer
  10454. sommer
  10455. bukala
  10456. sommer
  10457. somsak
  10458. somsak
  10459. ferrier
  10460. sonawane
  10461. sonawane
  10462. sonawane
  10463. bellur
  10464. ahuja
  10465. kulkarni
  10466. sonawane
  10467. harikisan
  10468. sonke
  10469. sonnenberger
  10470. sonnet
  10471. sonnet
  10472. sonoda
  10473. sonoda
  10474. sonoda
  10475. noboru
  10476. sorba
  10477. sorokin
  10478. sosna
  10479. sosnovsky
  10480. sotomayor
  10481. sotomayor
  10482. soucek
  10483. soucek
  10484. soumillion
  10485. soumillion
  10486. philippe
  10487. southgate
  10488. southgate
  10489. southwick
  10490. southwick
  10491. souto
  10492. souto
  10493. spada
  10494. spagnolo
  10495. spangler
  10496. spangler
  10497. spangler
  10498. spanton
  10499. spanton
  10500. spargo
  10501. spargo
  10502. spears
  10503. spears
  10504. speckamp
  10505. speckamp
  10506. speckamp
  10507. hiemstra
  10508. spencer
  10509. spero
  10510. spino
  10511. spino
  10512. spoerri
  10513. spoerri
  10514. dubois
  10515. sprecher
  10516. springs
  10517. spunta
  10518. squires
  10519. squires
  10520. srebnik
  10521. srinivasan
  10522. srivastava
  10523. srivastava
  10524. srivastava
  10525. clair
  10526. black
  10527. kumar
  10528. stacey
  10529. stacey
  10530. harris
  10531. stach
  10532. stach
  10533. hesse
  10534. stack
  10535. stadlbauer
  10536. stadlbauer
  10537. kappe
  10538. stadnichuk
  10539. stadnichuk
  10540. voropaeva
  10541. stadtmueller
  10542. stadtmueller
  10543. stefan
  10544. stafford
  10545. stafford
  10546. stahl
  10547. stahl
  10548. staib
  10549. stajer
  10550. stajer
  10551. stamford
  10552. stamford
  10553. stammer
  10554. stammer
  10555. stanczyk
  10556. standaert
  10557. stanek
  10558. stanek
  10559. stang
  10560. stang
  10561. stang
  10562. hanack
  10563. subramanian
  10564. stang
  10565. white
  10566. stankevich
  10567. stanovnik
  10568. stanovnik
  10569. starks
  10570. starks
  10571. starks
  10572. liotta
  10573. halpern
  10574. startsev
  10575. startsev
  10576. staszak
  10577. staszak
  10578. stauher
  10579. stauher
  10580. dehiak-krook
  10581. miller
  10582. steckhan
  10583. steckhan
  10584. steel
  10585. steel
  10586. steel
  10587. peter
  10588. steele
  10589. steele
  10590. steen
  10591. stefan
  10592. steglich
  10593. steglich
  10594. steinborn
  10595. steinborn
  10596. steinborn
  10597. stella
  10598. stephan
  10599. stephan
  10600. stephen
  10601. stephen
  10602. hillers
  10603. stephenson
  10604. stephenson
  10605. stepp
  10606. sternbach
  10607. sternbach
  10608. sterner
  10609. stetter
  10610. stetter
  10611. stetter
  10612. kuhlmann
  10613. stevens
  10614. stevens
  10615. stevenson
  10616. stevenson
  10617. wilson
  10618. stewart
  10619. stewart
  10620. benkovic
  10621. stewart
  10622. liotta
  10623. benkovic
  10624. stibr
  10625. stick
  10626. stidsen
  10627. stille
  10628. stille
  10629. stille
  10630. stille
  10631. stirling
  10632. stirling
  10633. stoddar
  10634. stoddar
  10635. stoddart
  10636. stoddart
  10637. stoddart
  10638. stoddart
  10639. zarzycki
  10640. stoddart
  10641. fraser
  10642. stokes
  10643. stoll
  10644. stolle
  10645. stolle
  10646. stoltefuss
  10647. stone
  10648. stork
  10649. stork
  10650. storr
  10651. stoss
  10652. stoss
  10653. hemmer
  10654. strauss
  10655. strazzolini
  10656. strazzolini
  10657. giumanini
  10658. cauci
  10659. streith
  10660. streith
  10661. streith
  10662. defoin
  10663. strekova
  10664. strittmatter
  10665. strohl
  10666. struchkov
  10667. strukul
  10668. strukul
  10669. struve
  10670. strzalko
  10671. strzalko
  10672. stuart
  10673. stuckwisch
  10674. stuckwisch
  10675. studabaker
  10676. stuhl
  10677. stumer
  10678. stumpf
  10679. sturgess
  10680. sturino
  10681. sturino
  10682. sturkovich
  10683. styrkovich
  10684. suami
  10685. suami
  10686. suami
  10687. ogawa
  10688. suarez
  10689. suarez
  10690. subhas
  10691. subramanian
  10692. sucheta
  10693. sucheta
  10694. suemune
  10695. suemune
  10696. suffert
  10697. sugasawa
  10698. sugimura
  10699. sugimura
  10700. suginome
  10701. suginome
  10702. sugiyama
  10703. sugiyama
  10704. sugiyama
  10705. suhas
  10706. suk-ku
  10707. suk-ku
  10708. suk-ku
  10709. sul'man
  10710. sul'man
  10711. sulikowski
  10712. sulikowski
  10713. sullivan
  10714. sullivan
  10715. sundaramurthy
  10716. sundberg
  10717. sundberg
  10718. sunjic
  10719. surkov
  10720. surpateaunu
  10721. surpateaunu
  10722. catteau
  10723. karafiloglou
  10724. lablache-combier
  10725. surya
  10726. surya
  10727. prakash
  10728. surzur
  10729. surzur
  10730. bertrand
  10731. susan
  10732. suschitzky
  10733. suschitzky
  10734. scriven
  10735. suschitzky
  10736. scriven
  10737. suska
  10738. suska
  10739. grajkowski
  10740. suslick
  10741. suslick
  10742. georg
  10743. suss-fink
  10744. suss-fink
  10745. suss-fink
  10746. meister
  10747. sustman
  10748. sustman
  10749. korth
  10750. suter
  10751. suter
  10752. weston
  10753. sutherland
  10754. sutherland
  10755. sutherland
  10756. sutton
  10757. sutton
  10758. suvorov
  10759. suzuki
  10760. suzuki
  10761. suzuki
  10762. suzuki
  10763. suzuki
  10764. suzuki
  10765. suzukib
  10766. svennson
  10767. svenson
  10768. sviridov
  10769. sviridov
  10770. svistunova
  10771. swain
  10772. swamer
  10773. swaminathan
  10774. swaminathan
  10775. narayanan
  10776. sweeney
  10777. sweeney
  10778. sweigart
  10779. swern
  10780. swern
  10781. swindell
  10782. swindell
  10783. swinger
  10784. swingle
  10785. syraeva
  10786. szabo
  10787. szabo
  10788. szafran
  10789. szafran
  10790. miroslaw
  10791. szajdzinska
  10792. szajdzinska
  10793. pietek
  10794. szeimies
  10795. szeverenyi
  10796. mukaiyama
  10797. sammmakia
  10798. taguchi
  10799. wagner-jauregg
  10800. ta-shma
  10801. ta-shma
  10802. rappoport
  10803. taber
  10804. taber
  10805. taber
  10806. taber
  10807. tachibana
  10808. tachibana
  10809. tackx
  10810. tackx
  10811. tadano
  10812. tadano
  10813. tadayoni
  10814. tadayoni
  10815. rebek
  10816. taeboem
  10817. tagliavini
  10818. taguchi
  10819. taguchi
  10820. takeo
  10821. takabe
  10822. takabe
  10823. kunihiko
  10824. takahashi
  10825. takahashi
  10826. takahashi
  10827. okazaki
  10828. takahashi
  10829. masaki
  10830. takahashi
  10831. takahashi
  10832. takahata
  10833. takahata
  10834. takahata
  10835. yamazaki
  10836. takahata
  10837. hiroki
  10838. takai
  10839. takai
  10840. kashi
  10841. takashima
  10842. takashima
  10843. takata
  10844. takata
  10845. takaya
  10846. takayama
  10847. takeda
  10848. takefumi
  10849. takemoto
  10850. takemoto
  10851. takemura
  10852. takemura
  10853. takenoshita
  10854. takenoshita
  10855. takeo
  10856. takeshi
  10857. takeshi
  10858. oriyama
  10859. takeshita
  10860. takeshita
  10861. takeuchi
  10862. takeuchi
  10863. takeya
  10864. takle
  10865. takle
  10866. takuwa
  10867. tamao
  10868. tamao
  10869. tamao
  10870. kobayashi
  10871. tamaru
  10872. tamaru
  10873. tamelen
  10874. jeker
  10875. tamminen
  10876. tamminen
  10877. tarja
  10878. tamotsu
  10879. tamura
  10880. tamura
  10881. tamura
  10882. tamura
  10883. kamimura
  10884. tamura
  10885. minamikawa
  10886. ikeda
  10887. tanaka
  10888. tanaka
  10889. tanaka
  10890. kazuhiko
  10891. tanaka
  10892. tanaka
  10893. tanaka
  10894. tandy
  10895. tandy
  10896. draper
  10897. taneja
  10898. tanemura
  10899. tanemura
  10900. tanis
  10901. tanko
  10902. tanko
  10903. tanner
  10904. tanner
  10905. tanner
  10906. tanyeli
  10907. tanyeli
  10908. tarak
  10909. tarasova
  10910. tarasova
  10911. tarasova
  10912. moskva
  10913. tarbell
  10914. tarbell
  10915. tarbet
  10916. targamadze
  10917. tarja
  10918. tarunin
  10919. taschner
  10920. taschner
  10921. tashiro
  10922. tashiro
  10923. tashtoush
  10924. tatarinova
  10925. tateiwa
  10926. tateiwa
  10927. taticchi
  10928. tatsuta
  10929. tatsuta
  10930. taylor
  10931. taylor
  10932. mckillop
  10933. taylor
  10934. turchi
  10935. taylor
  10936. taylor
  10937. taylor
  10938. taylor
  10939. tchoubar
  10940. tebben
  10941. tebben
  10942. tecilla
  10943. tedder
  10944. tedder
  10945. tedder
  10946. walton
  10947. tedford
  10948. tellier
  10949. templeton
  10950. templeton
  10951. templeton
  10952. tenhoeve
  10953. tenhoeve
  10954. terada
  10955. terao
  10956. terao
  10957. terashima
  10958. terashima
  10959. ishikura
  10960. ternansky
  10961. teruaki
  10962. teruo
  10963. testaferri
  10964. teuben
  10965. teuber
  10966. teuber
  10967. thangaraj
  10968. thangaraj
  10969. thatcher
  10970. thatcher
  10971. kluger
  10972. thebtaranonth
  10973. thebtaranonth
  10974. thebtaranonth
  10975. theil
  10976. theil
  10977. their
  10978. theopold
  10979. theopold
  10980. thibblin
  10981. thibblin
  10982. thibblin
  10983. ahlberg
  10984. thibblin
  10985. thickitt
  10986. thiem
  10987. thiem
  10988. klaffke
  10989. thieme
  10990. thiericke
  10991. thiericke
  10992. thomas
  10993. thomas
  10994. thomas
  10995. wright
  10996. thomas
  10997. bailey
  10998. thomas
  10999. raschke
  11000. thomas
  11001. thompson
  11002. thompson
  11003. green
  11004. thompson
  11005. thumme
  11006. thumme
  11007. thummel
  11008. thummel
  11009. thurley
  11010. thurston
  11011. thurston
  11012. thurston
  11013. thurston
  11014. david
  11015. thurston
  11016. ticcio
  11017. ticcio
  11018. tickner
  11019. tickner
  11020. tidwell
  11021. tidwell
  11022. tiecco
  11023. tiecco
  11024. tiecco
  11025. testaferri
  11026. tiedemann
  11027. tiedemann
  11028. tietze
  11029. tietze
  11030. tietze
  11031. beifuss
  11032. tikhonov
  11033. timashev
  11034. timberlake
  11035. timberlake
  11036. timofeeva
  11037. timofeeva
  11038. struchkov
  11039. timokhin
  11040. timokhin
  11041. timokhina
  11042. timoshchuk
  11043. timoshchuk
  11044. tingoli
  11045. tingoli
  11046. tipson
  11047. tiripicchio
  11048. tisler
  11049. tisler
  11050. tisler
  11051. stanovnik
  11052. tkachenko
  11053. tkhap
  11054. tochtermann
  11055. tochtermann
  11056. tochtermann
  11057. olsson
  11058. garratt
  11059. todres
  11060. todres
  11061. togni
  11062. togni
  11063. togni
  11064. pastor
  11065. togni
  11066. venanzi
  11067. tohru
  11068. tokuda
  11069. tokumaru
  11070. tokura
  11071. tokura
  11072. tollari
  11073. tollari
  11074. tolman
  11075. tolman
  11076. tolman
  11077. mckinney
  11078. tolstikov
  11079. tolstikov
  11080. tolstikov
  11081. tolstikov
  11082. borisova
  11083. cherkashin
  11084. komarov
  11085. arzama
  11086. tomalia
  11087. tomalia
  11088. tomalia
  11089. durst
  11090. tomalia
  11091. donald
  11092. tomas
  11093. tomilov
  11094. tomilov
  11095. dokichev
  11096. dzhemilev
  11097. nefedov
  11098. tomilov
  11099. tominaga
  11100. tominaga
  11101. tominaga
  11102. kohra
  11103. honkawa
  11104. hosomi
  11105. tominaga
  11106. shiroshita
  11107. hosomi
  11108. tomioka
  11109. tomioka
  11110. tommasi
  11111. tomooka
  11112. tomooka
  11113. tonani
  11114. tonellati
  11115. tonellato
  11116. tonellato
  11117. toner
  11118. toogood
  11119. toomey
  11120. toomey
  11121. toone
  11122. toone
  11123. simon
  11124. bednarski
  11125. whitesides
  11126. topsom
  11127. topsom
  11128. topuzyan
  11129. topuzyan
  11130. nesunts
  11131. torgasheva
  11132. torii
  11133. torii
  11134. torii
  11135. tanaka
  11136. inokuchi
  11137. torok
  11138. torok
  11139. toroman
  11140. toroman
  11141. toromanoff
  11142. toromanoff
  11143. toropova
  11144. torroba
  11145. torssell
  11146. torssell
  11147. toshiaki
  11148. toshima
  11149. toshima
  11150. tatsuta
  11151. toshimitsu
  11152. toshimitsu
  11153. toshio
  11154. toste
  11155. toste
  11156. totleb
  11157. touchard
  11158. toullec
  11159. toullec
  11160. toussaint
  11161. toussaint
  11162. touster
  11163. touster
  11164. townsend
  11165. townsend
  11166. townsend
  11167. townsend
  11168. tipson
  11169. toyota
  11170. toyota
  11171. fleming
  11172. trahanovsky
  11173. trahanovsky
  11174. tramontini
  11175. tramontini
  11176. tramontini
  11177. angiolini
  11178. traven
  11179. traven
  11180. shapakin
  11181. traylor
  11182. traylor
  11183. traynham
  11184. treger
  11185. treger
  11186. rozanov
  11187. tritzky
  11188. troev
  11189. troev
  11190. koljo
  11191. trofimov
  11192. trofimov
  11193. trofimov
  11194. mikhaleva
  11195. trofimov
  11196. rakhmatulina
  11197. gusarova
  11198. malysheva
  11199. trofimov
  11200. sokolyanskaya
  11201. senning
  11202. trogler
  11203. trogler
  11204. trommer
  11205. trommer
  11206. fleming
  11207. trost
  11208. trost
  11209. trost
  11210. trost
  11211. eming
  11212. trost
  11213. flemin
  11214. trost
  11215. fleming
  11216. trost
  11217. fleming
  11218. trost
  11219. fleming
  11220. pergamon
  11221. press
  11222. trost
  11223. leming
  11224. trost
  11225. merlic
  11226. trotter
  11227. troupel
  11228. truce
  11229. truce
  11230. truce
  11231. kreider
  11232. brand
  11233. trudell
  11234. trumbull
  11235. trzhtsinskaya
  11236. trzhtsinskaya
  11237. abramova
  11238. tsanaktsidis
  11239. tsanaktsidis
  11240. tsentalovich
  11241. tsentalovich
  11242. tskiyama
  11243. tsotinis
  11244. tsoungas
  11245. tsoungas
  11246. tsuchiya
  11247. tsuchiya
  11248. tsuchiya
  11249. tsuchiya
  11250. yoshikazu
  11251. tsuge
  11252. tsuge
  11253. kanemasa
  11254. tsuji
  11255. tsuji
  11256. minami
  11257. tsuji
  11258. nishida
  11259. tsuji
  11260. tsukayama
  11261. tsukayama
  11262. tsulciyama
  11263. tsumuraya
  11264. tsumuraya
  11265. batcheller
  11266. masamune
  11267. tsunoda
  11268. tsunoda
  11269. tsutomu
  11270. tsutomu
  11271. sugasawa
  11272. tsutsui
  11273. tsutsui
  11274. dubois
  11275. tsutsui
  11276. hancock
  11277. ariyoshi
  11278. tsutsumi
  11279. tsvetkov
  11280. tsypyshev
  11281. tucker
  11282. tucker
  11283. tumer
  11284. tumer
  11285. seniz
  11286. turbanova
  11287. turbanova
  11288. petrov
  11289. turchi
  11290. turnbull
  11291. turner
  11292. turner
  11293. turner
  11294. turos
  11295. turos
  11296. turro
  11297. turro
  11298. turro
  11299. tvaroska
  11300. tvaroska
  11301. bleha
  11302. tweel
  11303. twigg
  11304. twigg
  11305. tyler
  11306. tyler
  11307. tyler
  11308. uchida
  11309. uchida
  11310. udding
  11311. udding
  11312. udodong
  11313. uemura
  11314. uemura
  11315. motokazu
  11316. uemura
  11317. uenishi
  11318. uesaka
  11319. uesaka
  11320. azzena
  11321. uhlmann
  11322. uhlmann
  11323. peyman
  11324. ukaji
  11325. ukaji
  11326. ul'ev
  11327. ul'ev
  11328. shtefan
  11329. vvedenskii
  11330. ullrich
  11331. ulrich
  11332. umani-ronchi
  11333. umemoto
  11334. umemoto
  11335. teruo
  11336. undheim
  11337. undheim
  11338. undheim
  11339. benneche
  11340. undmann
  11341. ungvary
  11342. ungvary
  11343. unnovel
  11344. suzukib
  11345. untiedt
  11346. untiedt
  11347. unverzagt
  11348. unverzagt
  11349. carlo
  11350. uozumi
  11351. ur-rahman
  11352. ur-rahman
  11353. ur-rahman
  11354. urbam
  11355. urbam
  11356. urbanski
  11357. urbanski
  11358. urchegui
  11359. urchegui
  11360. ushiki
  11361. ushiki
  11362. timokhina
  11363. voronkov
  11364. timokhina
  11365. voronov
  11366. usyatinskii
  11367. usyatinskii
  11368. bregadze
  11369. utimoto
  11370. utimoto
  11371. uyehara
  11372. uyehara
  11373. uznanski
  11374. uznanski
  11375. blaszczyk
  11376. wieczorek
  11377. vaillancourt
  11378. vaillancourt
  11379. valerie
  11380. vaisman
  11381. valeev
  11382. valerie
  11383. valko
  11384. vallee
  11385. valli
  11386. valli
  11387. bekkum
  11388. kouwenhoven
  11389. broek
  11390. vermaas
  11391. heskamp
  11392. boeckel
  11393. steen
  11394. koten
  11395. dienst
  11396. bakker
  11397. engbersen
  11398. verboom
  11399. reinhoud
  11400. koten
  11401. verboom
  11402. reinhoudt
  11403. tamelen
  11404. veggel
  11405. verboom
  11406. reinhoudt
  11407. veggel
  11408. frank
  11409. vranken
  11410. vanaken
  11411. vanbekkum
  11412. vanderschaaf
  11413. vanderschaaf
  11414. vanderwalle
  11415. vanderwalle
  11416. clercq
  11417. vandeweghe
  11418. vandeweghe
  11419. vandort
  11420. vandort
  11421. vanhessche
  11422. vanhessche
  11423. vankoten
  11424. vankoten
  11425. vannieuwenhze
  11426. vannieuwenhze
  11427. sharpless
  11428. prasad
  11429. pillai
  11430. varfolomeev
  11431. varfolomeev
  11432. rainina
  11433. lozinskii
  11434. varinder
  11435. varma
  11436. varma
  11437. varney
  11438. varvoglis
  11439. varvoglis
  11440. baudin
  11441. panza
  11442. vasella
  11443. vasella
  11444. vasudevan
  11445. vasudevan
  11446. vasvari-debreczy
  11447. vedejs
  11448. vedejs
  11449. vedejs
  11450. krafft
  11451. vedejs
  11452. peterson
  11453. vedejs
  11454. veggel
  11455. veinberg
  11456. veinberg
  11457. lukevics
  11458. veith
  11459. veith
  11460. veldkamp
  11461. veldkamp
  11462. velichko
  11463. vellekoop
  11464. vellekoop
  11465. samuel
  11466. veltheer
  11467. venanzi
  11468. venepalli
  11469. venepalli
  11470. agosta
  11471. venkov
  11472. venkov
  11473. verboom
  11474. verboom
  11475. reinhoudt
  11476. verboom
  11477. willem
  11478. verdine
  11479. vergeychik
  11480. verhe
  11481. verhoeven
  11482. verkhovskaya
  11483. verkhovskaya
  11484. yamskov
  11485. verlag
  11486. vermaas
  11487. verweij
  11488. verweij
  11489. vroom
  11490. veschambre
  11491. veselovskii
  11492. vessieres
  11493. vicens
  11494. vicens
  11495. bohmer
  11496. vicens
  11497. jacques
  11498. vidari
  11499. vidari
  11500. viehe
  11501. viehe
  11502. viehe
  11503. viehe
  11504. janousek
  11505. viehe
  11506. merenyi
  11507. janousek
  11508. vigato
  11509. viktor
  11510. viktor
  11511. zhandankin
  11512. vilaplana
  11513. vilkov
  11514. villa
  11515. villa
  11516. villemin
  11517. villemin
  11518. vinader
  11519. vinnik
  11520. vinnik
  11521. obraztsov
  11522. vinogradov
  11523. vinogradova
  11524. vinsova
  11525. vinsova
  11526. viola
  11527. viola
  11528. collins
  11529. filippo
  11530. viout
  11531. virgil
  11532. virgil
  11533. visentin
  11534. vismara
  11535. viteva
  11536. viteva
  11537. vivona
  11538. vivona
  11539. buscemi
  11540. frenna
  11541. cusmano
  11542. vladuchick
  11543. vlasov
  11544. vlasov
  11545. vlasova
  11546. vlasova
  11547. voegtle
  11548. voegtle
  11549. voegtle
  11550. knops
  11551. vogel
  11552. vogel
  11553. vogel
  11554. vogel
  11555. fattori
  11556. gasparini
  11557. drian
  11558. vogtle
  11559. vogtle
  11560. vogtle
  11561. neumann
  11562. vohra
  11563. vohra
  11564. voitsekhovskii
  11565. vol'pin
  11566. vol'pin
  11567. akhrem
  11568. orlinkov
  11569. vol'pin
  11570. levitin
  11571. sigan
  11572. nikitaev
  11573. voladarsky
  11574. voladarsky
  11575. tikhonov
  11576. volke
  11577. volke
  11578. liska
  11579. volkov
  11580. volkov
  11581. volkov
  11582. vollhardt
  11583. vollhardt
  11584. volman
  11585. volman
  11586. volman
  11587. hammond
  11588. neckers
  11589. volodarskii
  11590. volodarskii
  11591. volodarsky
  11592. volodarsky
  11593. reznikov
  11594. ovcharenko
  11595. itzstein
  11596. vonseggern
  11597. vonseggern
  11598. vorbruggen
  11599. vorbruggen
  11600. vorbruggen
  11601. voronkov
  11602. voronkov
  11603. voronkov
  11604. dyakov
  11605. irpichenko
  11606. voronov
  11607. voropaeva
  11608. vorspohl
  11609. vostrowski
  11610. samarai
  11611. vrieze
  11612. vrieze
  11613. vroom
  11614. vuilleumier
  11615. vvedenskii
  11616. vygodskii
  11617. wulff
  11618. pearson
  11619. georg
  11620. thieme
  11621. verlag
  11622. russell
  11623. bowman
  11624. johnson
  11625. smadja
  11626. wulff
  11627. wachter
  11628. wachter
  11629. wachter-jurcsak
  11630. wachter-jurcsak
  11631. wadepohl
  11632. wadepohl
  11633. wadsworth
  11634. wadsworth
  11635. waghela
  11636. wagle
  11637. wagner
  11638. wagner
  11639. wagner-jauregg
  11640. wagner-jauregg
  11641. wahlberg
  11642. wahlberg
  11643. eklund
  11644. wailes
  11645. wailes
  11646. coutts
  11647. weigold
  11648. waiton
  11649. waiton
  11650. wakefield
  11651. wakselman
  11652. wakselman
  11653. walba
  11654. walba
  11655. walborsky
  11656. walborsky
  11657. waldemar
  11658. waldmann
  11659. waldmann
  11660. braun
  11661. waldmann
  11662. sebastian
  11663. walker
  11664. walker
  11665. walker
  11666. walker
  11667. wallace
  11668. wallace
  11669. wallbaum
  11670. wallbaum
  11671. wallbaum
  11672. martens
  11673. walling
  11674. walling
  11675. walling
  11676. huyser
  11677. walling
  11678. cheves
  11679. wallis
  11680. wallis
  11681. walsh
  11682. walsh
  11683. walsh
  11684. walter
  11685. walter
  11686. walter
  11687. schaumann
  11688. walters
  11689. walther
  11690. walther
  11691. walton
  11692. walton
  11693. walton
  11694. nicholas
  11695. wamhoff
  11696. wamhoff
  11697. wamhoff
  11698. dzenis
  11699. hirota
  11700. wanda
  11701. wandless
  11702. wuonola
  11703. robert
  11704. waring
  11705. waring
  11706. warkentin
  11707. warner
  11708. warner
  11709. warner
  11710. warner
  11711. warnhoff
  11712. warnhoff
  11713. korte
  11714. warren
  11715. warren
  11716. warrener
  11717. warrener
  11718. warsinsky
  11719. warsinsky
  11720. warwel
  11721. warwel
  11722. sojka
  11723. rusch
  11724. klaas
  11725. wasserman
  11726. wasserman
  11727. wasserman
  11728. clark
  11729. thurley
  11730. wasserman
  11731. watai
  11732. watai
  11733. watanabe
  11734. watanabe
  11735. watanabe
  11736. watkins
  11737. watson
  11738. watson
  11739. parshall
  11740. watts
  11741. waymouth
  11742. waymouth
  11743. wayne
  11744. wayner
  11745. wayner
  11746. parker
  11747. wilcox
  11748. thomas
  11749. weber
  11750. weber
  11751. weber
  11752. czugler
  11753. weber
  11754. toner
  11755. goldberg
  11756. vogtle
  11757. laidler
  11758. stoddart
  11759. weber
  11760. weber
  11761. weidenbruch
  11762. weidenbruch
  11763. weidmann
  11764. weidmann
  11765. seebach
  11766. weidner
  11767. weidner
  11768. weigold
  11769. weiler
  11770. weiler
  11771. weill-raynal
  11772. weill-raynal
  11773. weingarten
  11774. weingarten
  11775. weinges
  11776. weinges
  11777. weinig
  11778. weinig
  11779. weinreb
  11780. weinreb
  11781. weinreb
  11782. scola
  11783. weinreb
  11784. staib
  11785. weirich
  11786. weise
  11787. weiss
  11788. weiss
  11789. weiss
  11790. weiss
  11791. weiss
  11792. ramamurthy
  11793. hammond
  11794. weissberger
  11795. weissberger
  11796. laszlo
  11797. weitz
  11798. welch
  11799. welch
  11800. welch
  11801. eswarakrishnan
  11802. welker
  11803. weber
  11804. toner
  11805. goldberg
  11806. vogtle
  11807. laidler
  11808. stoddart
  11809. welker
  11810. wender
  11811. whaley
  11812. govindachari
  11813. wienreb@
  11814. wilds
  11815. williams
  11816. kurtz
  11817. winkler
  11818. wyrzykiewicz
  11819. lapucha
  11820. yamada
  11821. yamaguchi
  11822. yamashita
  11823. yamazaki
  11824. zefirov
  11825. beloglazkina
  11826. kutateladze
  11827. zimmer
  11828. lanken
  11829. horgan
  11830. welker
  11831. welle
  11832. welle
  11833. wellmaker
  11834. wellmaker
  11835. wells
  11836. weltner
  11837. weltner
  11838. wender
  11839. wender
  11840. ternansky
  11841. delong
  11842. singh
  11843. olivero
  11844. wenkert
  11845. wenkert
  11846. wentrup
  11847. wentrup
  11848. heilmayer
  11849. kollenz
  11850. wentrup
  11851. kambouris
  11852. werner
  11853. werner
  11854. werner
  11855. werner
  11856. erker
  11857. werner//erker
  11858. werstiuk
  11859. werstiuk
  11860. wessig
  11861. wessig
  11862. wessjohann
  11863. wessjohann
  11864. westerhausen
  11865. westerhausen
  11866. weston
  11867. weston
  11868. westwood
  11869. westwood
  11870. wetter
  11871. wetter
  11872. schleyer
  11873. weyenberg
  11874. whaley
  11875. whaley
  11876. govindachari
  11877. whaley
  11878. govindachari
  11879. whangbo
  11880. whetten
  11881. whitby
  11882. whitby
  11883. white
  11884. white
  11885. coville
  11886. white
  11887. whitesell
  11888. whitesell
  11889. whitesell
  11890. whitesell
  11891. whitesides
  11892. whitesides
  11893. mathias
  11894. whittaker
  11895. whitten
  11896. whitten
  11897. russell
  11898. schmehl
  11899. whittlesey
  11900. wiberg
  11901. wiberg
  11902. wiberg
  11903. wicha
  11904. widdowson
  11905. wieczorek
  11906. wielstra
  11907. wielstra
  11908. gambarotta
  11909. chiang
  11910. wiemer
  11911. wiemer
  11912. wierlacher
  11913. wierlacher
  11914. wiersum
  11915. wiersum
  11916. wigfield
  11917. wigfield
  11918. wiggins
  11919. wightmann
  11920. wijesekera
  11921. wijesekera
  11922. dolphin
  11923. wilcox
  11924. wilcox
  11925. craig
  11926. wilds
  11927. wilds
  11928. wilds
  11929. wilen
  11930. wilen
  11931. collet
  11932. jacques
  11933. wiley
  11934. wiley
  11935. england
  11936. wilhelm
  11937. wilke
  11938. wilkinson
  11939. wilkinson
  11940. stone
  11941. wilkinson
  11942. stone
  11943. wilkinson
  11944. willem
  11945. willett
  11946. willett
  11947. peter
  11948. william
  11949. william
  11950. lawson
  11951. william
  11952. crowe
  11953. william
  11954. parham
  11955. williams
  11956. williams
  11957. williams
  11958. harpp
  11959. williams
  11960. williams
  11961. williams
  11962. williams
  11963. williams
  11964. williams
  11965. williams
  11966. williams
  11967. williams
  11968. hendrix
  11969. williams
  11970. kurtz
  11971. williamson
  11972. williard
  11973. williard
  11974. willis
  11975. willis
  11976. wills
  11977. wills
  11978. wilman
  11979. wilman
  11980. wilson
  11981. wilson
  11982. wilson
  11983. wilson
  11984. schnapp
  11985. wilson
  11986. wimmer
  11987. winkler
  11988. winter
  11989. winter
  11990. winterfeldt
  11991. winterfeldt
  11992. wintner
  11993. wintner
  11994. rebek
  11995. wirthwein
  11996. wissing
  11997. wissing
  11998. witkop
  11999. roesky
  12000. wittenberger
  12001. wittenberger
  12002. witulski
  12003. witzel
  12004. wolber
  12005. folkers
  12006. wolfe
  12007. wolfe
  12008. ogliaruso
  12009. wolfe
  12010. wolfgang
  12011. wolfgang
  12012. herrmann
  12013. wollowitz
  12014. kajimoto
  12015. zhong
  12016. dumas
  12017. whitesides
  12018. tanko
  12019. hudlicky
  12020. woodgab
  12021. wovkulich
  12022. wozniak
  12023. wozniak
  12024. chojnowski
  12025. wozniak
  12026. wright
  12027. wulferding
  12028. wulferding
  12029. wulff
  12030. wulff
  12031. wulfman
  12032. wuonola
  12033. wustrow
  12034. peter
  12035. wyatt
  12036. wyman
  12037. wynberg
  12038. wynberg
  12039. wynberg
  12040. meijer
  12041. wyrzykiewicz
  12042. wyrzykiewicz
  12043. lapucha
  12044. yablokova
  12045. yablokova
  12046. aleksandrov
  12047. yadav
  12048. yadav
  12049. yagen
  12050. yagen
  12051. yagupol'skii
  12052. yahioglu
  12053. yakhontov
  12054. yakobson
  12055. yakobson
  12056. yakobson
  12057. furin
  12058. yakobson
  12059. vlasov
  12060. yalpani
  12061. yamada
  12062. yamada
  12063. yamada
  12064. yamada
  12065. yamada
  12066. tohru
  12067. yamaguchi
  12068. yamaguchi
  12069. miyazawa
  12070. takata
  12071. yamakawa
  12072. yamakawa
  12073. yamamoto
  12074. yamamoto
  12075. yamamoto
  12076. yamamoto
  12077. maruoka
  12078. yamamoto
  12079. maruoka
  12080. furuta
  12081. naruse
  12082. yamamoto
  12083. nozaki
  12084. yamamoto
  12085. yamamoto
  12086. yamamoto
  12087. yamamoto
  12088. yamamoto
  12089. yoshinori
  12090. yamanaka
  12091. yamanaka
  12092. sakamoto
  12093. niitsuma
  12094. yamashita
  12095. yamashita
  12096. yamashita
  12097. yamashita
  12098. yamataka
  12099. yamazaki
  12100. yamskov
  12101. yanada
  12102. yanada
  12103. yanada
  12104. harayama
  12105. yoneda
  12106. yanagida
  12107. yanagida
  12108. komori
  12109. yanagisawa
  12110. yanagisawa
  12111. yannoni
  12112. yanoff
  12113. yasuda
  12114. yasuda
  12115. yates
  12116. yates
  12117. loutfy
  12118. mckervey
  12119. yelamaggad
  12120. yelamaggad
  12121. yerxa
  12122. yeske
  12123. yoakim
  12124. hidemi
  12125. yokomatsu
  12126. yokomatsu
  12127. yokomatsu
  12128. yuasa
  12129. shibuya
  12130. yokoyama
  12131. yokoyama
  12132. yokoyama
  12133. imamoto
  12134. yokoyama
  12135. kondo
  12136. yonashiro
  12137. yoneda
  12138. yoneda
  12139. yonemitsu
  12140. mariano
  12141. yoshida
  12142. yoshida
  12143. yoshida
  12144. kamigata
  12145. yoshida
  12146. yoshifuji
  12147. yoshikawa
  12148. yoshikazu
  12149. yoshikoshi
  12150. yoshikoshi
  12151. miyashita
  12152. yoshinori
  12153. yoshio
  12154. yoshioka
  12155. yoshioka
  12156. parvez
  12157. miyazaki
  12158. parvez
  12159. yoshiro
  12160. younes
  12161. younes
  12162. metwally
  12163. elnagdi
  12164. young
  12165. young
  12166. young
  12167. douglas
  12168. young
  12169. stuart
  12170. yoursy
  12171. yoursy
  12172. sayed
  12173. yousef
  12174. yuasa
  12175. yuasa
  12176. yukito
  12177. yunusov
  12178. yunusov
  12179. yur'eva
  12180. yurtanov
  12181. yutin
  12182. yvonne
  12183. zabicky
  12184. zabicky
  12185. zabirov
  12186. zabirov
  12187. shamsevaleev
  12188. cherkasov
  12189. zablocka
  12190. zabotina
  12191. zahouily
  12192. zahouily
  12193. zaikov
  12194. zainullin
  12195. zajdel
  12196. zakrewski
  12197. zakrewski
  12198. zaman
  12199. zaman
  12200. sharma
  12201. zamaraev
  12202. zamecka-krakowiak
  12203. zander
  12204. zander
  12205. zangrando
  12206. zanirato
  12207. zappala
  12208. zarini
  12209. zarzycki
  12210. zassinovich
  12211. zassinovich
  12212. mestroni
  12213. gladiali
  12214. zaugg
  12215. zaugg
  12216. zaugg
  12217. martin
  12218. zavada
  12219. zbiral
  12220. zbiral
  12221. zecchi
  12222. zecchi
  12223. zeelen
  12224. zeelen
  12225. zefirov
  12226. zefirov
  12227. zefirov
  12228. palyulin
  12229. zefirov
  12230. zhdankin
  12231. koz'min
  12232. zefirov
  12233. beloglazkina
  12234. kutateladze
  12235. zefirov
  12236. nikolai
  12237. zehavi
  12238. zehavi
  12239. zeiler
  12240. zelichowicz
  12241. zeller
  12242. zemskov
  12243. zenneck
  12244. zenneck
  12245. zettlmeier
  12246. zhandankin
  12247. zhang
  12248. zhang
  12249. zhang
  12250. zhang
  12251. zhdankin
  12252. zhdanov
  12253. zhdanov
  12254. alekseev
  12255. kompantseva
  12256. vergeychik
  12257. zheng
  12258. zheng
  12259. zhengming
  12260. zhengming
  12261. zhong
  12262. tedford
  12263. hutchins
  12264. hutchins
  12265. ziche
  12266. zieger
  12267. zieger
  12268. ziegler
  12269. ziegler
  12270. zimmer
  12271. zimmer
  12272. lanken
  12273. horgan
  12274. zimmer
  12275. zimmerman
  12276. zimmerman
  12277. zimmerman
  12278. zimmermann
  12279. zimmmerman
  12280. zinczuk
  12281. zlotin
  12282. zlotin
  12283. luk'yanov
  12284. zlotin
  12285. naeva
  12286. luk'yanova
  12287. zobova
  12288. zoeller
  12289. zofia
  12290. zojaji
  12291. zollinger
  12292. zollinger
  12293. zollo
  12294. zolotukhina
  12295. zolotukhina
  12296. krutikov
  12297. lavrent'ev
  12298. zoltewicz
  12299. zoltewicz
  12300. zouhair
  12301. zschage
  12302. zucco
  12303. zuckermann
  12304. zuckermann
  12305. zuman
  12306. zuman
  12307. zwanenburg
  12308. zweifel
  12309. zweifel
  12310. brown
  12311. zweifel
  12312. miller
  12313. zydowsky
  12314. zydowsky
  12315. nikolai
  12316. solution
  12317. equilibrium
  12318. silicon
  12319. methoxypyridinium
  12320. salts
  12321. acyldihydropyridones
  12322. azoniaallene
  12323. cations
  12324. azadiene
  12325. quinone
  12326. diels
  12327. alder
  12328. oxidation
  12329. furoquinolinedion
  12330. cyclobutenyl
  12331. ketone
  12332. phenylthiocyclobutyl
  12333. ketone
  12334. hydrinad
  12335. tributylstannyl
  12336. glycals
  12337. organic
  12338. electrophiles
  12339. molecular
  12340. 1-azaspiro
  12341. 1-pyrroline
  12342. 1-pyrroline
  12343. annulation
  12344. pyrrolizidine
  12345. alkaloids
  12346. linked
  12347. oligos
  12348. 1.1.1
  12349. 1.5-hexadiynes
  12350. 10-ring
  12351. dioxides
  12352. 11-ring
  12353. academic
  12354. academic
  12355. press
  12356. research
  12357. account
  12358. account
  12359. research
  12360. accounts
  12361. accounts
  12362. accounts
  12363. chemical
  12364. research
  12365. accts
  12366. accts
  12367. acetic
  12368. acetic
  12369. derivatives
  12370. acids
  12371. scand
  12372. highlights
  12373. scanda
  12374. carbene
  12375. carbocation
  12376. chemistry
  12377. carbohydr
  12378. biochem
  12379. catal
  12380. cycloaddition
  12381. detailed
  12382. react
  12383. detailed
  12384. react
  12385. detailed
  12386. reaction
  12387. mechanisms
  12388. etal-organic
  12389. eterocycl
  12390. radical
  12391. terocycl
  12392. heterocycl
  12393. heterocyclic
  12394. synth
  12395. heterocyclic
  12396. metal-org
  12397. metal-org
  12398. metal-organic
  12399. molecular
  12400. modeling
  12401. ganomet
  12402. nomet
  12403. organomet
  12404. organomet
  12405. oxygenated
  12406. processes
  12407. photochem
  12408. silicon
  12409. silicon
  12410. chemistry
  12411. strain
  12412. organic
  12413. chemistry
  12414. supramolecular
  12415. chemistry
  12416. theor
  12417. theoretically
  12418. interesting
  12419. advance
  12420. advance
  12421. strain
  12422. organic
  12423. chemistry
  12424. advances
  12425. advances
  12426. advances
  12427. biophysical
  12428. chemistry
  12429. advances
  12430. carbanion
  12431. chemistry
  12432. advances
  12433. carbanion
  12434. chemistry
  12435. advances
  12436. carbene
  12437. chemistry
  12438. advances
  12439. cycloaddition
  12440. advances
  12441. cycloaddition
  12442. advances
  12443. dendritic
  12444. macromolecules
  12445. advances
  12446. detailed
  12447. reaction
  12448. mechanisms
  12449. advances
  12450. electron
  12451. transfer
  12452. chemistry
  12453. advances
  12454. heterocyclic
  12455. chemistry
  12456. advances
  12457. heterocyclic
  12458. natural
  12459. product
  12460. synthesis
  12461. advances
  12462. heterocyclic
  12463. natural
  12464. product
  12465. synthesis
  12466. advances
  12467. medicinal
  12468. chemistry
  12469. advances
  12470. medicinal
  12471. chemistry
  12472. advances
  12473. metal-organic
  12474. chemistry
  12475. advances
  12476. synthesis
  12477. advances
  12478. photochemistry
  12479. advances
  12480. physical
  12481. organic
  12482. chemistry
  12483. advances
  12484. silicon
  12485. chemistry
  12486. advances
  12487. strain
  12488. organic
  12489. chemistry
  12490. advances
  12491. strain
  12492. organic
  12493. chemistry
  12494. advances
  12495. supramolecular
  12496. chemistry
  12497. advances
  12498. synthons
  12499. organic
  12500. chemistr
  12501. advances
  12502. synthons
  12503. organic
  12504. chemistry
  12505. advances
  12506. theoretically
  12507. interesting
  12508. molecules
  12509. agents
  12510. aldehydes
  12511. chimica
  12512. aldrich
  12513. aldrich
  12514. aldrichimica
  12515. aldrichimica
  12516. alkaloids
  12517. alpha
  12518. chemie
  12519. angew
  12520. angew
  12521. angew
  12522. angew
  12523. angew
  12524. angew
  12525. angew
  12526. angew
  12527. photochem
  12528. anomeric
  12529. application
  12530. application
  12531. applications
  12532. applied
  12533. arenes
  12534. arenes
  12535. arines
  12536. arines
  12537. aspects
  12538. aspects
  12539. homogeneous
  12540. catalysis
  12541. etric
  12542. synthesis
  12543. stereodifferentiatin
  12544. reactions
  12545. asymm
  12546. ymmetr
  12547. synthesis
  12548. asymmetri
  12549. asymmetri
  12550. synthesis
  12551. stereodifferentiatin
  12552. reactions
  12553. asymmetric
  12554. asymmetric
  12555. synthes
  12556. asymmetric
  12557. synthesis
  12558. asymmetric
  12559. synthesis
  12560. asymmetric
  12561. synthesis
  12562. stereodifferentiatin
  12563. reactions
  12564. asymmetric
  12565. synthesis
  12566. stereodifferentiatin
  12567. reactions
  12568. asymmetry
  12569. autobiographies
  12570. bioactive
  12571. bioactive
  12572. molecules
  12573. biocatalysis
  12574. biochem
  12575. biochemistry
  12576. bioorganic
  12577. bioorganic
  12578. chemistry
  12579. frontiers
  12580. biophysical
  12581. bosons
  12582. britain
  12583. highlights
  12584. japan
  12585. highlights
  12586. highlights
  12587. highlights
  12588. france
  12589. c-radi
  12590. c-radi
  12591. c-radicals
  12592. highlights
  12593. carbanion
  12594. carbanions
  12595. carbene
  12596. carbenes
  12597. carbenes
  12598. enoids
  12599. carbenes
  12600. carbenoids
  12601. carbenoids
  12602. carbo
  12603. carbocation
  12604. carbocations
  12605. carbocations
  12606. carbocation
  12607. radicals
  12608. carbocyclic
  12609. carbocyclic
  12610. compo
  12611. chemistry
  12612. applications
  12613. carbocyclic
  12614. compounds
  12615. chemistry
  12616. applications
  12617. carbocyclic
  12618. compounds
  12619. chemistry
  12620. applications
  12621. carbocyclic
  12622. pi-electron
  12623. systems
  12624. carbohyd
  12625. carbohyd
  12626. highlights
  12627. carbohydr
  12628. carbohydrate
  12629. carbohydrate
  12630. research
  12631. carbohydrates
  12632. carbonic
  12633. carbonic
  12634. ivatives
  12635. carbonic
  12636. derivatives
  12637. carbonyl
  12638. carboxylic
  12639. carboxylic
  12640. acids
  12641. carbo
  12642. derivatives
  12643. carboxylic
  12644. acids
  12645. carboxylic
  12646. derivatives
  12647. carboxylic
  12648. acids
  12649. carboxylic
  12650. derivatives
  12651. catal
  12652. catalysis
  12653. catalysis
  12654. metal
  12655. complexes
  12656. catalytic
  12657. catalytic
  12658. oxidations
  12659. hydrogen
  12660. peroxide
  12661. oxidant
  12662. centers
  12663. chemE
  12664. london
  12665. highlights
  12666. letters
  12667. journal
  12668. synthetic
  12669. methods
  12670. pharm
  12671. japan
  12672. tract
  12673. tracts
  12674. chemical
  12675. chemie
  12676. chemis
  12677. chemistr
  12678. chemistry
  12679. chemistry
  12680. chemistry
  12681. chemistry
  12682. chemistry
  12683. britain
  12684. chemistry
  12685. letters
  12686. chemistry
  12687. heter
  12688. cyclic
  12689. compounds
  12690. chemistry
  12691. heterocyclic
  12692. compounds
  12693. chemistry
  12694. heterocyclic
  12695. compounds
  12696. chemists
  12697. chemtech
  12698. chemtra
  12699. chemtra
  12700. organic
  12701. chemistry
  12702. chemtracts
  12703. chemtracts
  12704. chemtracts
  12705. chemistry
  12706. chemtracts
  12707. organic
  12708. istry
  12709. chemtracts
  12710. organic
  12711. chemistry
  12712. chermistry
  12713. chermistry
  12714. heterocyclic
  12715. compounds
  12716. chimia
  12717. chimica
  12718. chirality
  12719. chirality
  12720. bosons
  12721. alpha
  12722. helix
  12723. chmeistry
  12724. chromatographic
  12725. chromatographic
  12726. science
  12727. series
  12728. prehensive
  12729. organic
  12730. synthesis
  12731. czech
  12732. highlights
  12733. czech
  12734. commun
  12735. collect
  12736. collect
  12737. czech
  12738. commun
  12739. communH
  12740. commun
  12741. compou
  12742. compoun
  12743. compound
  12744. compounds
  12745. compounds
  12746. comprehe
  12747. comprehe
  12748. organic
  12749. synthesis
  12750. comprehensiv
  12751. comprehensiv
  12752. organic
  12753. synthesis
  12754. comprehensive
  12755. comprehensive
  12756. comprehensive
  12757. comprehensive
  12758. rocyclic
  12759. chemistry
  12760. comprehensive
  12761. heterocyc
  12762. chemistry
  12763. comprehensive
  12764. heterocycl
  12765. chemistry
  12766. comprehensive
  12767. heterocycli
  12768. chemistry
  12769. comprehensive
  12770. heterocyclic
  12771. emistry
  12772. comprehensive
  12773. heterocyclic
  12774. chemis
  12775. comprehensive
  12776. heterocyclic
  12777. chemistry
  12778. comprehensive
  12779. heterocyclic
  12780. chemistry
  12781. comprehensive
  12782. ganic
  12783. chemistry
  12784. comprehensive
  12785. synthesis
  12786. comprehensive
  12787. chemistry
  12788. comprehensive
  12789. synthesis
  12790. comprehensive
  12791. organ
  12792. synthesis
  12793. comprehensive
  12794. organic
  12795. chemistry
  12796. comprehensive
  12797. organic
  12798. nthesis
  12799. comprehensive
  12800. organic
  12801. thesis
  12802. comprehensive
  12803. organic
  12804. synthes
  12805. comprehensive
  12806. organic
  12807. synthesi
  12808. comprehensive
  12809. organic
  12810. synthesis
  12811. comprehensive
  12812. organic
  12813. synthesis
  12814. comprehensive
  12815. organic
  12816. synthesis
  12817. derivatives
  12818. edit@
  12819. x-compounds
  12820. enoids@
  12821. etal-organic@
  12822. functional
  12823. helix
  12824. roarenes
  12825. heteroarenes
  12826. heteroatom
  12827. heterocycles
  12828. heterocycles
  12829. highlights@
  12830. heterocyclic
  12831. heterocyclic
  12832. compounds
  12833. series@
  12834. highlights
  12835. interesting@
  12836. highlights@
  12837. react
  12838. organic
  12839. organic
  12840. nitrogen
  12841. compounds
  12842. organo-pi-metal
  12843. compounds
  12844. acids
  12845. organic
  12846. chemistry
  12847. organomet
  12848. organometallics
  12849. rganic
  12850. synthesis
  12851. organosulfur
  12852. compounds
  12853. perkin
  12854. products
  12855. comprehensive
  12856. organic
  12857. synthesis
  12858. comprehensive
  12859. organic
  12860. synthesis
  12861. trost
  12862. comprehensive
  12863. organometallic
  12864. chemistry
  12865. comprehines
  12866. comprehines
  12867. hydrometallation
  12868. hydroboration
  12869. heterocyc
  12870. contemporary
  12871. contemporary
  12872. organic
  12873. synthesis
  12874. coord
  12875. coord
  12876. crown
  12877. crown
  12878. ethers
  12879. analogous
  12880. compounds
  12881. current
  12882. current
  12883. trends
  12884. organic
  12885. synthesis
  12886. cyclic
  12887. cycloa
  12888. cycloa
  12889. dition
  12890. reactions
  12891. carbohydrate
  12892. chemistry
  12893. cycloaddition
  12894. cycloaddition
  12895. reactions
  12896. carbohydrate
  12897. chemistry
  12898. czech
  12899. dendritic
  12900. derivatives
  12901. derivatives
  12902. detailed
  12903. dition
  12904. dreams
  12905. cycloaddition
  12906. pays-bas
  12907. eminent
  12908. emistry
  12909. x-compounds
  12910. pounds
  12911. x-comp
  12912. x-compounds
  12913. x-compounds
  12914. energetics
  12915. etal-organic
  12916. etallics
  12917. eterocycl
  12918. ethers
  12919. etric
  12920. heteroatom
  12921. excited
  12922. experientia
  12923. fluorinating
  12924. fluorine
  12925. fluorine-containing
  12926. fluorine-containing
  12927. molecules
  12928. structure
  12929. reactivity
  12930. synthesis
  12931. forschung
  12932. fortschritte
  12933. fortschritte
  12934. forschung
  12935. france
  12936. frontiers
  12937. funct
  12938. functional
  12939. functional
  12940. ganic
  12941. ganomet
  12942. phase
  12943. metal
  12944. reactions
  12945. ground
  12946. group
  12947. groups
  12948. hal/o
  12949. hal/o
  12950. n-acetals
  12951. hal/o
  12952. o/o-acetals
  12953. hal/o
  12954. n-acetals
  12955. hal/o
  12956. o/o-acetals
  12957. anomeri
  12958. helix
  12959. helix
  12960. highlights
  12961. hererocycles
  12962. hesis
  12963. hetarenes
  12964. hetarenes
  12965. hetarenes
  12966. hetarenes
  12967. ocycles
  12968. heter
  12969. hetero
  12970. hetero
  12971. hetero
  12972. renes
  12973. heteroarenes
  12974. heteroarenes
  12975. heteroarenes
  12976. heteroarenes
  12977. heteroarenes
  12978. heteroarenes
  12979. heteroarenes
  12980. heteroarenes
  12981. heteroarenes
  12982. heteroarenes
  12983. heteroarenes
  12984. heteroarenes
  12985. heteroarenes
  12986. heteroatom
  12987. heteroatom
  12988. heteroatom
  12989. chemistry
  12990. heterocy
  12991. heterocy
  12992. heterocyc
  12993. heterocycl
  12994. heterocycles
  12995. heterocycles
  12996. erocycles
  12997. highlights
  12998. heterocycli
  12999. heterocyclic
  13000. heterocyclic
  13001. ocyclic
  13002. compounds
  13003. series
  13004. highlights
  13005. highlights
  13006. homogeneous
  13007. houben
  13008. houben
  13009. hydroboration
  13010. hydrogen
  13011. hydrometallation
  13012. iates
  13013. indian
  13014. indian
  13015. ivatives
  13016. perkin
  13017. trans
  13018. trans
  13019. highlights
  13020. perkin
  13021. trans
  13022. highlights
  13023. perkin
  13024. trans
  13025. perkin
  13026. trans
  13027. uorine
  13028. fluorine
  13029. heterocycl
  13030. heterocycl
  13031. chemE
  13032. organomet
  13033. organomet
  13034. highlights
  13035. organomet
  13036. organometal
  13037. organometallic
  13038. scient
  13039. wiley
  13040. japan
  13041. perkin
  13042. perkin
  13043. quarterly
  13044. review
  13045. journ
  13046. journal
  13047. journal
  13048. physical
  13049. organic
  13050. chemistry
  13051. journal
  13052. physical
  13053. rganic
  13054. chemistry
  13055. klamann
  13056. letters
  13057. liebigs
  13058. liebigs
  13059. highlights
  13060. london
  13061. macromolecular
  13062. macromolecular
  13063. materials
  13064. macromolecules
  13065. manual
  13066. materials
  13067. mechanisms
  13068. medicinal
  13069. ments
  13070. metal
  13071. metal
  13072. promoted
  13073. selectivity
  13074. organic
  13075. synthesis
  13076. metal-org
  13077. metal-organic
  13078. metal-organic
  13079. methods
  13080. synthetic
  13081. methods
  13082. modeling
  13083. modern
  13084. modern
  13085. synthetic
  13086. methods
  13087. molecular
  13088. molecules
  13089. mprehensive
  13090. n-acetals
  13091. n-dou
  13092. n-double
  13093. reports
  13094. natural
  13095. natural
  13096. reports
  13097. natural
  13098. product
  13099. reports
  13100. natural
  13101. products
  13102. reports
  13103. nctional
  13104. fluorinating
  13105. agents
  13106. organic
  13107. thesis
  13108. fluorinating
  13109. agents
  13110. organic
  13111. synthesis
  13112. journ
  13113. journal
  13114. chemistry
  13115. trends
  13116. heterocyclic
  13117. chemistry
  13118. nitrogen
  13119. nomet
  13120. nthesis
  13121. nucleoside
  13122. nucleoside
  13123. synthesis
  13124. o/n-acetals
  13125. o/s-acetals
  13126. o/o-acetals
  13127. o/s-acetals
  13128. o/s-acetals
  13129. ocycles
  13130. omprehensive
  13131. omprehensive
  13132. organic
  13133. synthesis
  13134. procedure
  13135. react
  13136. react
  13137. react
  13138. react
  13139. reactions
  13140. organ
  13141. organ
  13142. nitrogen
  13143. compounds
  13144. organi
  13145. organic
  13146. organic
  13147. organic
  13148. organic
  13149. organic
  13150. electrochemistry
  13151. organic
  13152. nitrogen
  13153. compounds
  13154. organic
  13155. nitrogen
  13156. compounds
  13157. organic
  13158. nitrogen
  13159. compounds
  13160. organic
  13161. nitrogen
  13162. compounds
  13163. organic
  13164. nitrogen
  13165. compounds
  13166. n-dou
  13167. organic
  13168. nitrogen
  13169. compounds
  13170. n-double
  13171. organic
  13172. peroxides
  13173. organic
  13174. peroxy
  13175. organic
  13176. peroxy
  13177. compounds
  13178. organic
  13179. photochem
  13180. organic
  13181. preparations
  13182. procedures
  13183. organic
  13184. hesis
  13185. theory
  13186. applications
  13187. organic
  13188. synthesis
  13189. theory
  13190. organic
  13191. synthesis-theory
  13192. applications
  13193. organo
  13194. organo
  13195. etallics
  13196. manual
  13197. organo-pi-metal
  13198. organo-pi-metal
  13199. compounds
  13200. acids
  13201. organic
  13202. chemistry
  13203. organo-pi-metal
  13204. compounds
  13205. acids
  13206. organic
  13207. chemistry
  13208. organo-pi-metal
  13209. compounds
  13210. acids
  13211. rganic
  13212. chemistry
  13213. organoboron
  13214. organoboron
  13215. compounds
  13216. organoboron
  13217. compounds
  13218. organoboron
  13219. compounds
  13220. organoboron
  13221. compounds
  13222. organomet
  13223. organomet
  13224. organometal
  13225. organometal
  13226. organic
  13227. synthesis
  13228. organometallic
  13229. organometallic
  13230. chemistry
  13231. reviews
  13232. organometallic
  13233. compounds
  13234. organometallic
  13235. compounds
  13236. organometallic
  13237. compounds
  13238. organometallics
  13239. organometallics
  13240. manual
  13241. organometallics
  13242. highlights
  13243. organometallics
  13244. organic
  13245. synthesis
  13246. organometallics
  13247. rganic
  13248. synthesis
  13249. organophosphoru
  13250. organophosphoru
  13251. compounds
  13252. organophosphorus
  13253. organophosphorus
  13254. compounds
  13255. organophosphorus
  13256. compounds
  13257. organophosphorus
  13258. reagents
  13259. ganic
  13260. synthesis
  13261. organophosphorus
  13262. reagents
  13263. organic
  13264. synthesis
  13265. organoselenium
  13266. organoselenium
  13267. chemistry
  13268. organosilicon
  13269. organosilicon
  13270. compounds
  13271. organosulfur
  13272. organosulfur
  13273. compou
  13274. organosulfur
  13275. compounds
  13276. organosulfur
  13277. compounds
  13278. organotellurium
  13279. organotellurium
  13280. compoun
  13281. organotellurium
  13282. compounds
  13283. organotellurium
  13284. compounds
  13285. klamann
  13286. oxidant
  13287. oxidation
  13288. oxidation
  13289. organic
  13290. chemistry
  13291. oxidation
  13292. oxidations
  13293. oxygenated
  13294. patai
  13295. patai
  13296. series
  13297. pathways
  13298. pays-bas
  13299. peptides
  13300. periodical
  13301. perkin
  13302. perkin
  13303. peroxides
  13304. peroxy
  13305. pharm
  13306. pharmacol
  13307. phase
  13308. phosphorous
  13309. phosphorous
  13310. sulfur
  13311. photochem
  13312. photochemistry
  13313. photochemistry
  13314. organic
  13315. synthesis
  13316. photochemistry
  13317. phthalocyanines
  13318. phthalocyanines
  13319. properties
  13320. applications
  13321. physical
  13322. pi-electron
  13323. ports
  13324. posium-in-print
  13325. pounds
  13326. prehensive
  13327. prepC
  13328. rations
  13329. press
  13330. proced
  13331. dureC
  13332. procedures
  13333. processes
  13334. product
  13335. products
  13336. products
  13337. profiles
  13338. profiles
  13339. pathways
  13340. dreams
  13341. autobiographies
  13342. eminent
  13343. heterocyclic
  13344. progress
  13345. progress
  13346. heterocycl
  13347. chemistry
  13348. progress
  13349. heterocyclic
  13350. chemistry
  13351. progress
  13352. organic
  13353. chemistry
  13354. progress
  13355. chemistry
  13356. organic
  13357. natural
  13358. products
  13359. progress
  13360. chemistry
  13361. organic
  13362. natural
  13363. products
  13364. progress
  13365. chemistry
  13366. rganic
  13367. natural
  13368. products
  13369. promoted
  13370. 0-ipr@
  13371. 12-addition
  13372. imine@
  13373. 12-addition
  13374. aldehyde@
  13375. 12-diols
  13376. dipolar
  13377. cycloadditions
  13378. ethylthio
  13379. azetines
  13380. chlorides@
  13381. 13-dione@
  13382. 14-addition
  13383. 14-dehydroprostaglan@
  13384. 3478@
  13385. benzyloxy
  13386. cyclohexene
  13387. 6-ring
  13388. amino
  13389. organolithiums
  13390. amino
  13391. carbanions
  13392. lithiopiperidine@
  13393. review
  13394. review
  13395. expansion
  13396. methods
  13397. using
  13398. ylides
  13399. arene
  13400. alkyne
  13401. a-hydroxy
  13402. ketone@
  13403. abstraction
  13404. acetate
  13405. acetylenic
  13406. carbamate@
  13407. acids
  13408. acids/diels-alder@
  13409. acyl@
  13410. acyliminium
  13411. addition
  13412. adenines
  13413. albini
  13414. photocycloaddition
  13415. sensitization
  13416. physical
  13417. organic
  13418. alcohols
  13419. aldehyde
  13420. synthesis@
  13421. alder
  13422. aldol
  13423. chemistry@
  13424. alkaloid
  13425. alkene
  13426. alkenes
  13427. alkoxyaluminohydride@
  13428. alkylation
  13429. alkylidine@
  13430. alkynes
  13431. promoted
  13432. properties
  13433. promoted
  13434. react
  13435. reports
  13436. research
  13437. chemical
  13438. intermediates@
  13439. heteroatom
  13440. chem@
  13441. transl
  13442. scanda@
  13443. specialist@
  13444. states
  13445. studies@
  13446. symposium-in-print
  13447. synlett
  13448. synlett
  13449. journal
  13450. synthetic
  13451. methods@
  13452. synthes@
  13453. synthesis
  13454. synthetic
  13455. tetrahe
  13456. tetrahedron
  13457. tetrahedron
  13458. asymm@
  13459. tetredron
  13460. chemistry
  13461. functional
  13462. groups
  13463. stereochem
  13464. transfer@
  13465. transl
  13466. unctional
  13467. applied
  13468. chemistry
  13469. applied
  13470. chemistry
  13471. quarterly
  13472. quarterly
  13473. reviews
  13474. heteroatom
  13475. radical
  13476. radicals
  13477. rapoport
  13478. react
  13479. react
  13480. reaction
  13481. reactions
  13482. reactivity
  13483. reagents
  13484. rearrang
  13485. rearrang
  13486. ments
  13487. ground
  13488. excited
  13489. states
  13490. rearrangements
  13491. rearrangements
  13492. excited
  13493. states
  13494. rearrangements
  13495. ground
  13496. excited
  13497. states
  13498. pays-bas
  13499. pays-bas
  13500. recueil
  13501. recueil
  13502. recueil
  13503. recuiel
  13504. recuiel
  13505. reduction
  13506. reduction
  13507. reduction
  13508. register
  13509. renes
  13510. reports
  13511. reports
  13512. intermed
  13513. research
  13514. research
  13515. chemical
  13516. interme
  13517. iates
  13518. research
  13519. chemical
  13520. intermedia
  13521. research
  13522. chemical
  13523. intermediates
  13524. heteroatom
  13525. heteroatom
  13526. heteroatom
  13527. review
  13528. review
  13529. reviews
  13530. reviews
  13531. heteroatom
  13532. chemistry
  13533. react
  13534. rganic
  13535. rganic
  13536. peroxy
  13537. compounds
  13538. roarenes
  13539. rocyclic
  13540. transl
  13541. transl
  13542. transl
  13543. trans
  13544. transl
  13545. transl
  13546. scanda
  13547. science
  13548. scient
  13549. selective
  13550. selective
  13551. organic
  13552. transformation
  13553. selectivity
  13554. series
  13555. silicon
  13556. silicon
  13557. compounds
  13558. egister
  13559. review
  13560. silicon
  13561. compounds
  13562. register
  13563. review
  13564. smolin
  13565. smolin
  13566. rapoport
  13567. states
  13568. stereo
  13569. stereoc
  13570. stereochem
  13571. stereodifferentiatin
  13572. strain
  13573. strategies
  13574. strategies
  13575. tactics
  13576. synthesis
  13577. strategies
  13578. tactics
  13579. organic
  13580. synthesis
  13581. structural
  13582. structural
  13583. chemistry
  13584. structure
  13585. studies
  13586. studies
  13587. natural
  13588. products
  13589. chemistry
  13590. studies
  13591. natural
  13592. products
  13593. chemistry
  13594. studies
  13595. natural
  13596. products
  13597. chemistry
  13598. bioactive
  13599. natur
  13600. studies
  13601. organic
  13602. chemistry
  13603. sulfur
  13604. sulfur
  13605. ports
  13606. sulfur
  13607. reports
  13608. supramolecular
  13609. thesis
  13610. symposium-in-print
  13611. symposium-in-print
  13612. commun
  13613. hesis
  13614. synform
  13615. synlett
  13616. synlett
  13617. synth
  13618. commun
  13619. highlights
  13620. synth
  13621. commun
  13622. journal
  13623. synthetic
  13624. methods
  13625. synth
  13626. peptides
  13627. synthes
  13628. synthes
  13629. synthesi
  13630. synthesis
  13631. synthesis
  13632. synthesis
  13633. synthesis
  13634. synthesis
  13635. highlights
  13636. synthesis
  13637. journal
  13638. synthetic
  13639. methods
  13640. synthesis
  13641. peptides
  13642. synthesis
  13643. peptides
  13644. synthesis
  13645. peptides
  13646. synthesis-theory
  13647. synthetic
  13648. synthetic
  13649. synthons
  13650. systems
  13651. tactics
  13652. terocycl
  13653. highlights
  13654. letters
  13655. tetra
  13656. tetra
  13657. edron
  13658. tetrahe
  13659. tetrahe
  13660. tetrahe
  13661. tetrahed
  13662. tetrahed
  13663. tetrahedr
  13664. tetrahedr
  13665. tetrahedro
  13666. tetrahedron
  13667. tetrahedron
  13668. tetrahedron
  13669. asymmetry
  13670. tetrahedron
  13671. asymmetry
  13672. highlights
  13673. tetrahedron
  13674. highlights
  13675. tetrahedron
  13676. highlights
  13677. tetrahedron
  13678. posium-in-print
  13679. tetrahedron
  13680. symposium-in-print
  13681. tetredron
  13682. tetredron
  13683. tetredron
  13684. tetrehedron
  13685. tetrehedron
  13686. highlights
  13687. alkaloids
  13688. pharm
  13689. alkaloids
  13690. pharmacol
  13691. chemistry
  13692. functional
  13693. groups
  13694. chemistry
  13695. functional
  13696. groups
  13697. chemistry
  13698. carbonyl
  13699. group
  13700. chemistry
  13701. nctional
  13702. groups
  13703. chemistry
  13704. functional
  13705. groups
  13706. chemistry
  13707. functional
  13708. groups
  13709. chemistry
  13710. unctional
  13711. groups
  13712. chmeistry
  13713. functional
  13714. groups
  13715. total
  13716. synthesis
  13717. natural
  13718. products
  13719. organometallic
  13720. compound
  13721. organic
  13722. synthesis
  13723. organometallic
  13724. compound
  13725. organi
  13726. synthesis
  13727. organometallic
  13728. compound
  13729. organic
  13730. synthesis
  13731. theor
  13732. theoretically
  13733. theory
  13734. thesis
  13735. stereo
  13736. stereoc
  13737. stereochem
  13738. stereochem
  13739. topics
  13740. topics
  13741. topics
  13742. current
  13743. topics
  13744. current
  13745. chemistry
  13746. topics
  13747. stereochem
  13748. total
  13749. total
  13750. synthesis
  13751. natural
  13752. products
  13753. tract
  13754. tracts
  13755. trans
  13756. transformation
  13757. transl
  13758. transl
  13759. trends
  13760. trost
  13761. unctional
  13762. unctional
  13763. unknown
  13764. uorine
  13765. various
  13766. wiley
  13767. x-comp
  13768. x-compounds
  13769. ynthesis
  13770. Pro 2.0 - 2.1F!
  13771. Pro 3.0
  13772. US English - Spelling
  13773. addition
  13774. ketone
  13775. asymmetric
  13776. induction
  13777. reductive
  13778. alkylation
  13779. acyclic
  13780. radical
  13781. dienes
  13782. epoxides
  13783. methanolysis
  13784. oxazines
  13785. transposed
  13786. allylic
  13787. alcohols
  13788. substituted
  13789. tetramethylethyle
  13790. transposed
  13791. allylic
  13792. alcohols
  13793. trimethylsilyl
  13794. group
  13795. organic
  13796. 12-addi
  13797. 12-addit
  13798. 12-addition
  13799. imine
  13800. 12-diols
  13801. 12-oxazole
  13802. 12-rin
  13803. 12-ring
  13804. 12-th
  13805. 12-ylides
  13806. tetrazines
  13807. cyclopenta
  13808. tetrazines
  13809. azodiazo
  13810. 124-butanetriol
  13811. biradicals
  13812. substitution
  13813. methylphenyl
  13814. triazene
  13815. solvents
  13816. methanol
  13817. dienes
  13818. dipolar
  13819. cyclo
  13820. addition
  13821. antibacterial
  13822. agents
  13823. azomethine
  13824. dipolar
  13825. cyclo
  13826. additions
  13827. diels
  13828. alder
  13829. reactions
  13830. diastereofa
  13831. dipolar
  13832. cycloaddition
  13833. cycloaddition
  13834. benzopyran
  13835. dipolar
  13836. cycloaddition
  13837. alcohols
  13838. dipolar
  13839. cycloadditions
  13840. dipolar
  13841. cycloadditions
  13842. ethylthio
  13843. azetines
  13844. chlorides
  13845. dithianes
  13846. 13-aminoalcohol
  13847. 13-asymmetric
  13848. 13-asymmetric
  13849. induction
  13850. 13-benzothiazines
  13851. 13-di
  13852. 13-diketone
  13853. 13-diol
  13854. 13-diol
  13855. synthesis
  13856. 13-dioxolane
  13857. 13-dioxoles
  13858. 13-dipolar
  13859. 13-dipolar
  13860. cycloaddition
  13861. 13-dipoles
  13862. 13-dithiane
  13863. 13-dithianes
  13864. 13-oxazoles
  13865. 13-propanedionata
  13866. 13-propanedionato
  13867. 13-thiazoles
  13868. 134-selenadiazolines
  13869. 134-thiadizolines
  13870. addition
  13871. dialdehyde
  13872. diels
  13873. alder
  13874. furan
  13875. oxabicyclic
  13876. opening
  13877. elimination
  13878. 14-addition
  13879. 14-addition
  13880. 14-addition
  13881. reaction
  13882. 14-cyclohexadiene
  13883. 14-dichloro-2-butene
  13884. 14-dihydropyridines
  13885. 14-diol
  13886. 14-reduction
  13887. 14-reduction
  13888. enones
  13889. 14-ring
  13890. 14881
  13891. asymmetric
  13892. induction
  13893. transmetalation
  13894. 15-c-h
  13895. 15-dipolar
  13896. 15-dipoles
  13897. 15-ring
  13898. 16-diketone
  13899. 18-cr-6
  13900. 18-crown-6
  13901. nzene
  13902. alkene
  13903. photochemistry
  13904. intramolecular
  13905. diradical
  13906. cycloaddition
  13907. imine
  13908. lactam
  13909. enolate
  13910. cycloaddition
  13911. synthesis
  13912. review
  13913. photocycloaddition
  13914. wolff
  13915. diazo
  13916. target
  13917. hydroquinone
  13918. synthesis
  13919. ketene
  13920. alkoxy
  13921. alkynyl
  13922. carbonates
  13923. amino
  13924. butadienes
  13925. azapentadienyl
  13926. anion
  13927. boronation
  13928. allyl
  13929. borane
  13930. aldehyde
  13931. azoniaallene
  13932. salts
  13933. cycloadditions
  13934. bromomethyl
  13935. aziridines
  13936. allylamines
  13937. radical
  13938. induced
  13939. cyclo
  13940. additions
  13941. carbonyl
  13942. compounds
  13943. alkenes
  13944. stereocontrol
  13945. cyclo-addition/tolue
  13946. isocyanate/trichloro
  13947. isocyanate/glyca
  13948. ethoxy
  13949. phase
  13950. silyloxypyrrole
  13951. aldehyde
  13952. aldol
  13953. pyrrole
  13954. lactam
  13955. substituted
  13956. cycloalkane
  13957. dione
  13958. cyclic
  13959. ketoester
  13960. 2-alkyltetrahydropyr
  13961. 2-aminobenzophenone
  13962. 2-arylpropionic
  13963. 2-carboxylic
  13964. 2-carboxylic
  13965. 2-chlorobenzoxazoliu
  13966. 2-chloropyridinium
  13967. 2-cyanopyridinium
  13968. 2-cyclopenten-1-ones
  13969. 2-fluorobenzothiazol
  13970. 2-fluoropyridinium
  13971. 2-hydroxytetrahydrop
  13972. 2-oxazolin-5-ones
  13973. 2-oxoazetidine
  13974. 2-pyridones
  13975. 2.1.2.1.2.1
  13976. 2.2.0
  13977. 2.2.1
  13978. benzisoxazoles
  13979. reduction
  13980. cyclization
  13981. trichloroethyl
  13982. 2266-tetramethylpipe
  13983. cohols
  13984. sigmatropic
  13985. rearrangement
  13986. wittig
  13987. rearrangement
  13988. wittig
  13989. rearrangement
  13990. allyl
  13991. anion
  13992. sulfide
  13993. reductive
  13994. cleava
  13995. wittig
  13996. sigmatropic
  13997. rearrangement
  13998. 23-dipolar
  13999. 23-disubstituted
  14000. 23-disubstituted
  14001. indole
  14002. synthesis
  14003. 23-wittig
  14004. 23-wittig
  14005. rearrangement
  14006. 25/75
  14007. 26-dihydroxypiperidi
  14008. ycloaddition
  14009. cycloaddition
  14010. methylenecyclopropan
  14011. cycloadditions
  14012. electron
  14013. transfer
  14014. reactions
  14015. dipolar
  14016. cycloaddition
  14017. cyclization
  14018. methoxy
  14019. phenyl
  14020. dioxolane
  14021. protecting
  14022. group
  14023. aldehyd
  14024. cycloaddition
  14025. tetramic
  14026. acids
  14027. methodology
  14028. hydroxymethylindole
  14029. indole
  14030. ionization
  14031. cation
  14032. cycloaddit
  14033. substitution
  14034. sulfolenes
  14035. 3-alkoxyacrolein
  14036. 3-dipolar
  14037. 3-isoxazolyl
  14038. 3-isoxazolyl
  14039. ether
  14040. 3-methyl-24-pentaned
  14041. 3-ring
  14042. 3.2.0
  14043. 3.3.0
  14044. 3.3.1
  14045. sigmatropic
  14046. rearrangement
  14047. disubstituted
  14048. indole
  14049. disubstituted
  14050. pyrroles
  14051. 34-benzodiazocines
  14052. cycloadditions
  14053. addition
  14054. reactions
  14055. cycloaddition
  14056. amino
  14057. oxadiazolines
  14058. oxadiazoles
  14059. benzyloxy
  14060. cyclohexene
  14061. benzyloxy
  14062. cyclohexene
  14063. oxoalkanoates
  14064. chloropropenyl
  14065. ketones
  14066. activated
  14067. cyclopropan
  14068. participation
  14069. butadienes
  14070. azadienes
  14071. 4-chromanone
  14072. 4-dimethylaminopyrid
  14073. 4-dimethylaninopyrid
  14074. 4-imidazolidone
  14075. 4-methoxy-benzyl
  14076. 4-methylene-13-dioxa
  14077. 4-methylene-13-dioxo
  14078. 4-pyridones
  14079. 4-ring
  14080. 4.2.0
  14081. 4.2.1
  14082. 44-disubstituted
  14083. 45-dihydrodioxepins
  14084. 4h-13-dioxins
  14085. pentanone
  14086. levulinate
  14087. memebered
  14088. carbocycle
  14089. carbamoylpolyoxamic
  14090. derivatives
  14091. 5-endo-dig
  14092. 5-endo-dig
  14093. cyclization
  14094. 5-endo-trig
  14095. 5-endo-trig
  14096. cyclization
  14097. 5-exo
  14098. 5-exo-dig
  14099. 5-exo-dig
  14100. cyclization
  14101. 5-rin
  14102. 5-ring
  14103. 5.2.0
  14104. 6-exo
  14105. 6-exo
  14106. cyclization
  14107. 6-ring
  14108. 6-ring
  14109. 61405
  14110. 660631
  14111. cycloaddition
  14112. disrotatory
  14113. closure
  14114. 7-oxa
  14115. 7-oxa
  14116. pgf2a
  14117. 14-dehydroprostaglan
  14118. 7-ring
  14119. membered
  14120. cyclic
  14121. lactone
  14122. synthesis
  14123. 8-phenylmenthol
  14124. 8-ring
  14125. borabicyclo
  14126. 3.3.1
  14127. nonane
  14128. reductions
  14129. 9-phenylfluoren-9-yl
  14130. 900482
  14131. amino
  14132. acids
  14133. photochemistry
  14134. aminoketones
  14135. amino
  14136. organolithiums
  14137. amino
  14138. carbanions
  14139. lithiopiperidine
  14140. epoxyalkyl
  14141. trimethylsilane
  14142. reactions
  14143. epoxysulfoxide
  14144. sulfide
  14145. unsaturated
  14146. unsaturated
  14147. carbonyl
  14148. compounds
  14149. chemistry
  14150. unsaturated
  14151. esters
  14152. cyclic
  14153. depsipeptide
  14154. lyngbya
  14155. majuscula
  14156. unsaturated
  14157. esters
  14158. stereochemical
  14159. control
  14160. carbonyl
  14161. compo
  14162. unsaturated
  14163. sulfone
  14164. b-unsaturated
  14165. b-unsaturated
  14166. aldehyde
  14167. b-unsaturated
  14168. carbonyl
  14169. compound
  14170. b-unsaturated
  14171. ester
  14172. b-unsaturated
  14173. ketone
  14174. b-unsaturated
  14175. lactone
  14176. bromo
  14177. ketones
  14178. vinyliminophosphoran
  14179. halogenoketones
  14180. chloroacetic
  14181. dibromoethane
  14182. hydroxy
  14183. carbonyl
  14184. compounds
  14185. epoxides
  14186. esters
  14187. walker
  14188. sulfoxide
  14189. oxidation
  14190. sulfides
  14191. carbanion
  14192. additio
  14193. kainic
  14194. acetals
  14195. dialkoxy
  14196. imines
  14197. protected
  14198. diones
  14199. review
  14200. review
  14201. review
  14202. recent
  14203. routes
  14204. amino
  14205. acids
  14206. enantiosel
  14207. review
  14208. synthetic
  14209. chiral
  14210. azitridines
  14211. review
  14212. photoinduced
  14213. electron
  14214. transfer
  14215. review
  14216. expansion
  14217. methods
  14218. using
  14219. ylides
  14220. arene
  14221. alkyne
  14222. sulfinyl
  14223. radicals
  14224. addition
  14225. reactions
  14226. substituted
  14227. radicals
  14228. sulfonyl
  14229. anions
  14230. survey
  14231. various
  14232. stoichiometric
  14233. catalytic
  14234. asymmetric
  14235. a-acetoxy
  14236. a-acetoxy
  14237. copper-zinc
  14238. reagents
  14239. a-alkoxy
  14240. a-alkoxy
  14241. aldehyde
  14242. a-alkoxyl
  14243. a-amide
  14244. a-amide
  14245. sulfone
  14246. a-amido
  14247. a-amido
  14248. sulfide
  14249. a-amino
  14250. a-amino
  14251. ketone
  14252. synthesis
  14253. a-aminocopper
  14254. a-aminocopper
  14255. carbanion
  14256. a-aminolithium
  14257. a-aminolithium
  14258. carbanion
  14259. a-benzyloxy
  14260. a-benzyloxy
  14261. thioester
  14262. a-bromo
  14263. a-bromo
  14264. silyl
  14265. alcohol
  14266. a-bromoamide
  14267. a-chloro
  14268. a-chloro
  14269. epoxide
  14270. a-chloro
  14271. ketone
  14272. a-cyano
  14273. a-cyano
  14274. methylether
  14275. a-ester
  14276. a-formyl
  14277. a-formyl
  14278. ester
  14279. a-glucosides
  14280. a-haloketone
  14281. a-hydrostannylation
  14282. a-hydroxy
  14283. a-hydroxy
  14284. a-hydroxy
  14285. cyclopropane
  14286. a-hydroxy
  14287. ester
  14288. a-hydroxy
  14289. ketone
  14290. a-hydroxyamide
  14291. a-hydroxylation
  14292. a-hyroxyketone
  14293. a-hyroxyketone
  14294. synthesis
  14295. a-keto
  14296. a-lactam
  14297. a-lithio
  14298. a-lithio
  14299. sulfoxides
  14300. a-lithio-nitriles
  14301. a-metallated
  14302. a-metallated
  14303. carbamate
  14304. a-nitro
  14305. a-nitro
  14306. ketone
  14307. a-nitroso
  14308. a-phenylthio-g
  14309. a-phenylthio-g
  14310. d-unsaturated
  14311. ketone
  14312. a-pyrone
  14313. a-silyl
  14314. a-silyl
  14315. alcohol
  14316. a-silyl
  14317. ether
  14318. a-silylketone
  14319. a-thio-isobenzofuran
  14320. a-thiolactones
  14321. a-trimethylsilyloxy
  14322. initio
  14323. calculations
  14324. gharbia
  14325. nitrone
  14326. dipolar
  14327. cycloaddition
  14328. dipole
  14329. ketene
  14330. abramovitch
  14331. absence
  14332. absolute
  14333. absolute
  14334. constants
  14335. multiple
  14336. substitutions
  14337. chain
  14338. chlorin
  14339. absolute
  14340. expressions
  14341. homolytic
  14342. substitution
  14343. consta
  14344. absorption
  14345. abstraction
  14346. abstraction
  14347. accelerated
  14348. accelerated
  14349. vinylcyclopropane
  14350. rearrangement
  14351. aliphatic
  14352. claise
  14353. acceleration
  14354. acceptor
  14355. access
  14356. acene
  14357. acetal
  14358. drolysis
  14359. acetal
  14360. initiated
  14361. vinlysilane
  14362. terminated
  14363. polyene
  14364. cationic
  14365. acetal
  14366. opening
  14367. acetalisation
  14368. acetals
  14369. acetalsroh
  14370. acetamide
  14371. acetamide
  14372. heterocycle
  14373. cyano
  14374. synthesis
  14375. review
  14376. pyrrole
  14377. acetate
  14378. acetate
  14379. acetic
  14380. anhydride
  14381. chemistry
  14382. acetic
  14383. anhydride
  14384. sulfoxides
  14385. acetoacetylation
  14386. acetogenins
  14387. acetoguanamides
  14388. acetoguanamines
  14389. acetoguanides
  14390. acetone
  14391. acetonide
  14392. acetonides
  14393. acetonitrile
  14394. acetoxy
  14395. acetylacetonate/mono
  14396. acetylation
  14397. acetylcyclohexene
  14398. acetylene
  14399. acetylene
  14400. iodocyclization
  14401. acetylene
  14402. alkene
  14403. acetylenedicarboxyla
  14404. acetylenes
  14405. acetylenes
  14406. azoniaallene
  14407. salts
  14408. benzophenanthridines
  14409. acetylenic
  14410. acetylenic
  14411. alcohol
  14412. acetylenic
  14413. carbamate
  14414. acetylenic
  14415. ester
  14416. acetylenic
  14417. ethers
  14418. stannylcupration
  14419. acetylenic
  14420. ketone
  14421. acetylenic
  14422. silane
  14423. acetylenic
  14424. thioether
  14425. acetylide
  14426. sodium
  14427. alkylation
  14428. carbanion
  14429. review
  14430. alkyne
  14431. addition
  14432. acetylneuraminate
  14433. achiwa
  14434. achiwa
  14435. review
  14436. chiral
  14437. asymmetric
  14438. hydrogenation
  14439. reduction
  14440. construction
  14441. cycliza
  14442. derivatives
  14443. precursors
  14444. acidic
  14445. acids
  14446. acids/diels-alder
  14447. acridines
  14448. acrolein
  14449. acromelalga
  14450. acrylate
  14451. acrylates
  14452. acrylic
  14453. acrylonitrile
  14454. actions
  14455. activated
  14456. activated
  14457. copper
  14458. activated
  14459. magnesium
  14460. activating
  14461. activation
  14462. active
  14463. active
  14464. chromium
  14465. complexed
  14466. benzaldehyde
  14467. stereoselective
  14468. active
  14469. salen
  14470. manganese
  14471. complexes
  14472. catalytic
  14473. asymmetric
  14474. active
  14475. salen
  14476. manganese
  14477. complexes
  14478. enantioselective
  14479. epoxid
  14480. activity
  14481. acyclic
  14482. acyclic
  14483. dienes
  14484. organic
  14485. halides
  14486. norbornadiene
  14487. complexes
  14488. acyclic
  14489. stereocontrol
  14490. erythro
  14491. selectivity
  14492. acyclic
  14493. stereoselection
  14494. absolute
  14495. configuration
  14496. condensation
  14497. anion
  14498. equivalent
  14499. aziridine
  14500. acylating
  14501. dianion
  14502. polydetides
  14503. ester
  14504. cyanides
  14505. iminium
  14506. review
  14507. introduction
  14508. generation
  14509. elimi
  14510. migration
  14511. nitroso
  14512. compounds
  14513. alpha
  14514. chloronitroso
  14515. compounds
  14516. natural
  14517. pyrone
  14518. radicals
  14519. silane
  14520. silane
  14521. silicon
  14522. review
  14523. method
  14524. carbanion
  14525. addition
  14526. carbony
  14527. thioamide
  14528. acylamino
  14529. acylating
  14530. acylation
  14531. reduction
  14532. acylcarbonium
  14533. acyldihydropyridones
  14534. acylethenyl
  14535. acyliminium
  14536. acyliminium
  14537. acylnitroso
  14538. acyloins
  14539. acyloxylation
  14540. acylpalladium
  14541. acylsilanes
  14542. alkane
  14543. strain
  14544. nitrogen
  14545. extrusion
  14546. diradical
  14547. review
  14548. dimethyldioxirane
  14549. dioxirane
  14550. epoxidation
  14551. oxygen
  14552. transfer
  14553. dioxetane
  14554. chemiluminescence
  14555. decomposition
  14556. formaldehyde
  14557. dioxetane
  14558. synthesis
  14559. photochem
  14560. chemiluminescence
  14561. review
  14562. dioxirane
  14563. oxidation
  14564. review
  14565. epoxide
  14566. epoxidation
  14567. singlet
  14568. oxygen
  14569. review
  14570. sharpless
  14571. review
  14572. reagent
  14573. oxidation
  14574. ketone
  14575. reactivity
  14576. mechanism
  14577. synthesis
  14578. alkane
  14579. diazo
  14580. photochem
  14581. thermal
  14582. novel
  14583. review
  14584. adamantane
  14585. adamantanylidene
  14586. adamantylidene
  14587. additio
  14588. additionD
  14589. addition
  14590. addition
  14591. cyclopropanes
  14592. addition
  14593. stereoselective
  14594. nonchelation
  14595. controlled
  14596. reagent
  14597. addition
  14598. aldehyde
  14599. ketone
  14600. addition/cyclization
  14601. additions
  14602. additions
  14603. carbon
  14604. additive
  14605. addtion
  14606. adduct
  14607. adducts
  14608. adenines
  14609. adenines
  14610. adenines
  14611. hypoxanthines
  14612. guanines
  14613. isoguanines
  14614. xanthines
  14615. theobr
  14616. adenosines
  14617. adiabatic
  14618. adine
  14619. adrenoceptor
  14620. adriamycin
  14621. affinity
  14622. afford
  14623. after
  14624. agclo4
  14625. agent
  14626. agents
  14627. agents
  14628. chlorotrimethylsilan
  14629. deprotection
  14630. peterson
  14631. alkene
  14632. synthesis
  14633. silicon
  14634. alcohol
  14635. olefin
  14636. silicon
  14637. review
  14638. alkene
  14639. equivalent
  14640. alkylation
  14641. carbanion
  14642. aggregate
  14643. aggregation
  14644. aggregation
  14645. lithium
  14646. amide
  14647. aggregation
  14648. state
  14649. aglycon
  14650. agonist
  14651. agosta
  14652. klynes
  14653. al2o3
  14654. alane
  14655. albendazole
  14656. albini
  14657. albini
  14658. photocycloaddition
  14659. sensitization
  14660. physical
  14661. organic
  14662. albizati
  14663. albright
  14664. albright
  14665. carbanion
  14666. alkylation
  14667. amine
  14668. amino
  14669. nitrile
  14670. review
  14671. albus
  14672. alcohol
  14673. erification
  14674. radical
  14675. reduction
  14676. alcohol
  14677. epimerization
  14678. alcohol
  14679. inversion
  14680. alcohol
  14681. synthesis
  14682. alcoholes
  14683. alcohols
  14684. alcohols
  14685. alcohols
  14686. hydroxymethylation
  14687. stereochemistry
  14688. product
  14689. silicon
  14690. alcohols
  14691. lactams
  14692. esters
  14693. aldehyde
  14694. aldehyde
  14695. acetylene
  14696. carbonyl
  14697. addition
  14698. acetylide
  14699. optically
  14700. aldehyde
  14701. condensation
  14702. aldehyde
  14703. coupling
  14704. aldehyde
  14705. selectivity
  14706. reated
  14707. variety
  14708. lewis
  14709. promote
  14710. aldehyde
  14711. synthesis
  14712. aldehydes
  14713. alder
  14714. alder
  14715. cycloadditions
  14716. occurring
  14717. terpene
  14718. derivatives
  14719. modeling
  14720. aldimine
  14721. aldol
  14722. aldol
  14723. chemistry
  14724. aldol
  14725. complexes
  14726. aldehydes
  14727. aldol
  14728. condensation
  14729. diastereoselective
  14730. aldol
  14731. coupling
  14732. reaction
  14733. aldol
  14734. cyclization
  14735. aldol
  14736. reaction
  14737. aldol
  14738. reaction
  14739. amino
  14740. acids
  14741. aldol
  14742. reaction
  14743. condensation
  14744. aldol
  14745. reaction
  14746. samarium
  14747. enolate
  14748. aldol
  14749. reactions
  14750. aldol
  14751. closure
  14752. aldol
  14753. closure
  14754. aldoxime
  14755. aldrich
  14756. alfred
  14757. aliphatic
  14758. alkali
  14759. alkaline
  14760. alkaliod
  14761. alkaloid
  14762. alkaloid
  14763. diene
  14764. azide
  14765. intramolecular
  14766. dipolar
  14767. cycloaddition
  14768. alkaloid
  14769. synthesis
  14770. alkaloids
  14771. alkaloids
  14772. naltrexone
  14773. alkane
  14774. alkane
  14775. dehydrogenation
  14776. complexes
  14777. carbonylation
  14778. aldehydes
  14779. alkanes
  14780. alkanones
  14781. alkehydes
  14782. alken
  14783. alkeneF
  14784. alkene
  14785. formation
  14786. arenesulfonoxyamine
  14787. alkene
  14788. anhydride
  14789. amide
  14790. ester
  14791. carbonyl
  14792. review
  14793. wittig
  14794. phosphor
  14795. alkene
  14796. aziridine
  14797. nitrene
  14798. silane
  14799. alpha
  14800. amino
  14801. ketone
  14802. alkene
  14803. metathesis
  14804. alkene
  14805. osmium
  14806. dihydroxylation
  14807. asymmetric
  14808. alpha
  14809. dihydrox
  14810. alkene
  14811. synthesis
  14812. alkenes
  14813. alkenes
  14814. alkenic
  14815. alkenoates
  14816. alkenyl
  14817. alkenylamines
  14818. alkenylboranes
  14819. alkenylborates
  14820. alkenylcyclopropyl
  14821. alkenylketone
  14822. alkenylstannanes
  14823. alkinylcarbene
  14824. alklyation
  14825. alkohol
  14826. alkoholes
  14827. alkohols
  14828. alkoxide
  14829. alkoxide
  14830. induced
  14831. reaction
  14832. phase
  14833. transfer
  14834. catalysis
  14835. carbonyl
  14836. alkoxides
  14837. alkoxy
  14838. alkoxy
  14839. radical
  14840. alkoxyallenes
  14841. alkoxyaluminium
  14842. alkoxyaluminohydride
  14843. alkoxyamines
  14844. alkoxycarbonylation
  14845. alkoxycarbonylazoalk
  14846. alkoxycarbonylazoalk
  14847. aminocarbonylazoalke
  14848. tosylhydrazones
  14849. alkoxymethyl
  14850. alkoxymethyl
  14851. oxime
  14852. ether
  14853. alkoxypalladation
  14854. alkyl
  14855. alkyl
  14856. azide
  14857. cerium
  14858. alkyl
  14859. migration
  14860. alkyl
  14861. phenyl
  14862. sulfones
  14863. allylic
  14864. sulfones
  14865. aldehydes
  14866. alkyl
  14867. radicals
  14868. alkyla
  14869. alkylation
  14870. alkylation
  14871. alkylation
  14872. silyl
  14873. ketene
  14874. acetal
  14875. alkylations
  14876. alkylidenation
  14877. alkylidene
  14878. alkylidene
  14879. transfer
  14880. reagents
  14881. alkylidenecyclopropa
  14882. alkylidine
  14883. alkylidine
  14884. complexes
  14885. annulation
  14886. alkyllithium
  14887. alkyllithiums
  14888. alkylpyridinium
  14889. alkylsilanes
  14890. alkyn
  14891. alkyne
  14892. alkoxide
  14893. addition
  14894. digonal
  14895. intramolecular
  14896. alkyne
  14897. diphenylditelluride
  14898. bistelluroalkene
  14899. cuprate
  14900. subst
  14901. alkyne
  14902. equivalent
  14903. sulfone
  14904. sulfonyl
  14905. acetylene
  14906. cycloaddition
  14907. alkyne
  14908. mediated
  14909. cyclization
  14910. alkyne
  14911. enone
  14912. nickel
  14913. coupling
  14914. conjugate
  14915. addition
  14916. mechanis
  14917. alkynes
  14918. alkynes
  14919. alkynoates
  14920. alkynyl
  14921. alkynyl
  14922. stannane
  14923. iodonium
  14924. sulfinate
  14925. addition
  14926. vinyl
  14927. alkynylamines
  14928. alkynylborates
  14929. alkynylcarbene
  14930. alkynylcyclobutenone
  14931. alkynyliodonium
  14932. alkynyliodonium
  14933. alkyul
  14934. allen
  14935. allen
  14936. allene
  14937. allene
  14938. alkyne
  14939. sigmatropic
  14940. enyne
  14941. diradical
  14942. bergman
  14943. radic
  14944. allene
  14945. amino
  14946. amine
  14947. oxide
  14948. sigmatropic
  14949. indole
  14950. rearr
  14951. allene
  14952. epoxidation
  14953. dimethyldioxirene
  14954. epoxide
  14955. review
  14956. cyclizat
  14957. allene
  14958. ester
  14959. halide
  14960. cross
  14961. coupling
  14962. palladium
  14963. boron
  14964. suzuki
  14965. allene
  14966. furan
  14967. intramolecular
  14968. alkyne
  14969. isomerization
  14970. propargyl
  14971. allene
  14972. furan
  14973. intramolecular
  14974. diels
  14975. alder
  14976. isoindole
  14977. heterocycl
  14978. allene
  14979. intramolecular
  14980. addition
  14981. heterocycle
  14982. hydrazine
  14983. cycliza
  14984. allene
  14985. organolithium
  14986. addition
  14987. alpha
  14988. amino
  14989. aldehydes
  14990. tbuok
  14991. allene
  14992. closure
  14993. rrangement
  14994. pericyclic
  14995. review
  14996. allene
  14997. sulfone
  14998. chloro
  14999. trichloro
  15000. activated
  15001. facile
  15002. diels
  15003. allene
  15004. synthesis
  15005. allenecarboxylate
  15006. allenes
  15007. allenes
  15008. benzenethiol
  15009. allyl
  15010. radicals
  15011. allenes
  15012. carbopalladation
  15013. allyl
  15014. palladium
  15015. diene
  15016. cycliza
  15017. allenes
  15018. iodides
  15019. allenic
  15020. allenyl
  15021. allenylboronate
  15022. allenylcarboxamides
  15023. allenylmethyl
  15024. allenylmethyl
  15025. trimethylsilane
  15026. allenyltin
  15027. allenyltin
  15028. reagent
  15029. allics
  15030. allinger
  15031. allium
  15032. alloy
  15033. allylF
  15034. SEARCHVARIABLE7
  15035. allene
  15036. ester
  15037. halide
  15038. cross
  15039. coupling
  15040. palladium
  15041. boron
  15042. suzuki
  15043. allene
  15044. sigmatropic
  15045. rearrangement
  15046. pericyclic
  15047. review
  15048. allyl
  15049. allyl
  15050. alcohol@
  15051. allyl
  15052. silane
  15053. spiro
  15054. michael
  15055. addition
  15056. nazarov
  15057. cyclopentenone
  15058. allyl
  15059. reagent@
  15060. allylic
  15061. allylic
  15062. acetate@
  15063. allylic
  15064. cation
  15065. reduction
  15066. silane
  15067. deoxygenation
  15068. lithium
  15069. perchl@
  15070. allylsilane
  15071. allylstannanes@
  15072. alpha
  15073. alpha
  15074. hydrogens
  15075. boron
  15076. reagent
  15077. imines
  15078. organocopper
  15079. diene@
  15080. aluminium
  15081. aluminum
  15082. complex@
  15083. amberlyst@
  15084. arene
  15085. metal
  15086. complexes
  15087. coordinated
  15088. arenes
  15089. nucleophilic
  15090. aromatic
  15091. organolithium
  15092. arsindoles@
  15093. arylation
  15094. asymmetric
  15095. asymmetric
  15096. diels-alder
  15097. reaction@
  15098. asymmetric
  15099. propargyl
  15100. alcohol
  15101. synthesis@
  15102. asymmetric
  15103. synthesis
  15104. vinyl
  15105. sulfoxides
  15106. enantioselective
  15107. synth@
  15108. authors
  15109. david
  15110. hannessian
  15111. topics
  15112. organotin
  15113. organotin
  15114. aza-robinson
  15115. annulation@
  15116. azide
  15117. synthesis
  15118. allyl
  15119. allyl
  15120. amine
  15121. allyl
  15122. borane
  15123. allyl
  15124. boration
  15125. allyl
  15126. bromide
  15127. allyl
  15128. carbonate
  15129. allyl
  15130. cuprate
  15131. allyl
  15132. esters
  15133. alcohols
  15134. analogs
  15135. bonds
  15136. acids
  15137. allyl
  15138. ether
  15139. allyl
  15140. ethers
  15141. allyl
  15142. grignard
  15143. allyl
  15144. halide
  15145. allyl
  15146. iodide
  15147. allyl
  15148. lithium
  15149. allyl
  15150. magnesium
  15151. reagent
  15152. allyl
  15153. metal
  15154. allyl
  15155. phenol
  15156. allyl
  15157. phosphates
  15158. allyl
  15159. silane
  15160. allyl
  15161. silane
  15162. silicon
  15163. benzylic
  15164. cation
  15165. migration
  15166. silyl
  15167. cyclope
  15168. allyl
  15169. silane
  15170. spiro
  15171. michael
  15172. addition
  15173. nazarov
  15174. cyclopentenone
  15175. allyl
  15176. stannane
  15177. allyl
  15178. sulfide
  15179. allyl
  15180. sulfide
  15181. sulfone
  15182. radical
  15183. samarium
  15184. annulation
  15185. carbo
  15186. allyl
  15187. sulfides
  15188. allyl
  15189. sulfone
  15190. equivalent
  15191. anion
  15192. sulfonyl
  15193. introduction
  15194. reducti
  15195. allyl
  15196. allyl
  15197. tributylstannane
  15198. lamine
  15199. allylamines
  15200. allylamines
  15201. amination
  15202. esters
  15203. amines
  15204. allylamines
  15205. allenes
  15206. wittig
  15207. horner
  15208. reaction
  15209. enamines
  15210. derivati
  15211. allylation
  15212. allylation
  15213. carbonyl
  15214. stereochem
  15215. synclinal
  15216. antiperiplanar
  15217. allylboration
  15218. allylboronate
  15219. allylcarboxylic
  15220. allylchromium
  15221. allylchromium
  15222. reagent
  15223. allylcomp
  15224. allylic
  15225. allylic
  15226. allylic
  15227. alcohol
  15228. synthesis
  15229. allylic
  15230. alcohols
  15231. asymmetric
  15232. epoxidation
  15233. efficient
  15234. synthesis
  15235. allylic
  15236. alcohols
  15237. unsaturated
  15238. allylic
  15239. alkylations
  15240. allylic
  15241. amine
  15242. allylic
  15243. cation
  15244. reduction
  15245. silane
  15246. deoxygenation
  15247. lithium
  15248. perchl
  15249. allylic
  15250. allylic
  15251. ethers
  15252. allylic
  15253. halides
  15254. alpha
  15255. halocarbanions
  15256. allylsilanes
  15257. allyltin
  15258. allylic
  15259. mesylate
  15260. allylic
  15261. metalation
  15262. allylic
  15263. organocopper
  15264. reagents
  15265. alpha
  15266. methyl
  15267. ester
  15268. conjugat
  15269. allylic
  15270. phosphates
  15271. allylic
  15272. sulfones
  15273. allylic
  15274. zirconium
  15275. reagents
  15276. forming
  15277. reaction
  15278. thioaldehyd
  15279. allyllithiums
  15280. allylmetal
  15281. allylmetal
  15282. reagent
  15283. allyloxy
  15284. allyloxy
  15285. radicals
  15286. convenient
  15287. method
  15288. expansion
  15289. allylpalladium
  15290. allylsilane
  15291. allylsilane
  15292. allylsilane
  15293. aldehyde
  15294. condensation
  15295. allylsilane
  15296. synthesis
  15297. allylsilanes
  15298. allylsilanes
  15299. equivalent
  15300. stannanes
  15301. chemistry
  15302. allenes
  15303. silicon
  15304. allylstannane
  15305. ylstannanes
  15306. allyltin
  15307. allyltin
  15308. vinyl
  15309. carbene
  15310. monoterpene
  15311. lewis
  15312. bifunctional
  15313. allyltributylstannan
  15314. allyltributylstannan
  15315. trimethylsilyl
  15316. cyanide
  15317. epoxy
  15318. aldehy
  15319. allyltrimethylsilane
  15320. allylzirconium
  15321. allylzirconium
  15322. reagent
  15323. alonso
  15324. alonso
  15325. metal
  15326. diazo
  15327. transition
  15328. writing
  15329. cycloaddition
  15330. cyclopro
  15331. alpha
  15332. alpha
  15333. alpha
  15334. alkoxy
  15335. radical
  15336. cyclization
  15337. tetrahydropyran
  15338. formation
  15339. alpha
  15340. amino
  15341. acids
  15342. venom
  15343. alkaloids
  15344. asymmetric
  15345. synthesis
  15346. alpha
  15347. amino
  15348. acids
  15349. organometallic
  15350. addition
  15351. reactions
  15352. progenit
  15353. alpha
  15354. amino
  15355. acids
  15356. pseudomonas
  15357. fluorescens
  15358. aminophenylal
  15359. alpha
  15360. amino
  15361. aldehydes
  15362. erythro
  15363. sphingosine
  15364. threo
  15365. sphingos
  15366. alpha
  15367. amino
  15368. alkoxides
  15369. ortho
  15370. lithiation
  15371. alpha
  15372. unsaturated
  15373. carbonyl
  15374. compound
  15375. acylethenyl
  15376. anion
  15377. alpha
  15378. unsaturated
  15379. carbonyl
  15380. compounds
  15381. natural
  15382. product
  15383. alpha
  15384. unsaturated
  15385. ketones
  15386. photochemical
  15387. cycloaddition
  15388. alpha
  15389. unsaturated
  15390. thione
  15391. dimers
  15392. diels
  15393. alder
  15394. reaction
  15395. alpha
  15396. catalysts
  15397. enantioselectivity
  15398. auxiliaries
  15399. alpha
  15400. chloroketone
  15401. lithium
  15402. perchlorate
  15403. solvolysis
  15404. oxallyl
  15405. alpha
  15406. hydrogens
  15407. boron
  15408. reagent
  15409. imines
  15410. organocopper
  15411. diene
  15412. alpha
  15413. ester
  15414. quebrachitol
  15415. aldol
  15416. reaction
  15417. cyclitol
  15418. alpha
  15419. mannosidase
  15420. inhibitor
  15421. quinolizidine
  15422. alkaloids
  15423. swainson
  15424. alpha
  15425. nitro
  15426. ketones
  15427. alpha
  15428. unsaturated
  15429. carbonyl
  15430. compound
  15431. alpha
  15432. silyl
  15433. amine
  15434. photosensitization
  15435. alpha
  15436. amino
  15437. radical
  15438. alpha
  15439. substituted
  15440. alkanones
  15441. promoted
  15442. reactions
  15443. medium
  15444. alpha
  15445. radical
  15446. chiral
  15447. reaction
  15448. allyl
  15449. stannane
  15450. alpha
  15451. thioether
  15452. oxonium
  15453. silane
  15454. cyclization
  15455. tetrahyd
  15456. alpha-acetoxy
  15457. alpha-alkoxyalkylati
  15458. alpha-aminophosphoni
  15459. alpha-aminophosphoni
  15460. acids/diels-alder
  15461. reactions/asymmetric
  15462. alpha-chloro-e-croty
  15463. alpha-cleavage
  15464. alpha-cyanothioaceta
  15465. alpha-hydride
  15466. alpha-hydroxylamino
  15467. alpha-methoxy-e-crot
  15468. alpha-methyl-e-croty
  15469. alpha-n-amidoalkylat
  15470. alpha-sulfinylenones
  15471. alteration
  15472. alternative
  15473. alumina
  15474. aluminium
  15475. aluminium
  15476. aluminium
  15477. isopropoxide
  15478. rearrangement
  15479. aluminum
  15480. reagent
  15481. aluminum
  15482. reagents
  15483. amalgam
  15484. amaryllidaceae
  15485. amberlyst
  15486. ambident
  15487. ambient
  15488. ambient
  15489. temperature
  15490. ambiphilicity
  15491. american
  15492. amide
  15493. amide
  15494. alkene
  15495. catalyzed
  15496. cyclization
  15497. lactam
  15498. amide
  15499. alpha
  15500. radicals
  15501. transfer
  15502. cyclization
  15503. addition
  15504. amide
  15505. coupling
  15506. bop-cl
  15507. amide
  15508. coupling
  15509. procedure
  15510. amide
  15511. enolate
  15512. chiral
  15513. aniline
  15514. protonation
  15515. asymmetric
  15516. amide
  15517. enolate
  15518. chiral
  15519. aniline
  15520. protonation
  15521. asymmetric
  15522. amide
  15523. lactam
  15524. radical
  15525. cyclization
  15526. heterocycle
  15527. metal
  15528. intra
  15529. amide
  15530. lactam
  15531. thioamides
  15532. thiolactam
  15533. thionation
  15534. alternative
  15535. amide
  15536. dienolate
  15537. amide
  15538. lactam
  15539. synthesis
  15540. amide
  15541. phosphine
  15542. ligand
  15543. amidine
  15544. amidine
  15545. carbenoid
  15546. epoxide
  15547. carbene
  15548. review
  15549. imine
  15550. diazo
  15551. azometh
  15552. amidines
  15553. amido
  15554. amidoalkylation
  15555. amidocarbonylation
  15556. amidrazone
  15557. amidyl
  15558. amidyl
  15559. radical
  15560. cyclization
  15561. nitrile
  15562. addition
  15563. rearrangement
  15564. aminals
  15565. amination
  15566. amineE
  15567. amine
  15568. ulfones
  15569. amine
  15570. aluminum
  15571. alkyul
  15572. aluminum
  15573. amide
  15574. acylation
  15575. me3al
  15576. amine
  15577. enone
  15578. photochemical
  15579. abstraction
  15580. alpha
  15581. amino
  15582. radical
  15583. amine
  15584. protection
  15585. amine
  15586. synthesis
  15587. amines
  15588. aminium
  15589. aminium
  15590. precursors
  15591. amino
  15592. amino
  15593. amino
  15594. synthesis
  15595. amino
  15596. synthesis
  15597. amino
  15598. acids
  15599. amino
  15600. acids
  15601. dimethylhydrazones
  15602. alkylation
  15603. amino
  15604. acids
  15605. stereoselective
  15606. synthesis
  15607. ozonide
  15608. fragmentation
  15609. amino
  15610. alcohol
  15611. amino
  15612. alcohol
  15613. catalyst
  15614. amino
  15615. alcohol
  15616. oxazine
  15617. threitol
  15618. chiral
  15619. auxiliaries
  15620. amino
  15621. amino
  15622. amine
  15623. diazo
  15624. chiral
  15625. ketone
  15626. rhodium
  15627. carbenoid
  15628. ammonium
  15629. amino
  15630. cyclization
  15631. amino
  15632. ester
  15633. synthesis
  15634. amino
  15635. nitrile
  15636. synthesis
  15637. amino-alcohol
  15638. amino-alcohol
  15639. synthesis
  15640. amino-aldol
  15641. amino-aldol
  15642. reaction
  15643. aminoacetals
  15644. aminoalcohol
  15645. aminoalcohol
  15646. aminoalcohol
  15647. synthesis
  15648. aminoaldehyde
  15649. aminoalkyl
  15650. aminobenzotriazoles
  15651. aminocarbonylazoalke
  15652. aminocyclitol
  15653. aminocyclitol
  15654. synthesis
  15655. aminocyclization
  15656. aminocyclopropane
  15657. aminocyclopropanecar
  15658. aminodiazonium
  15659. aminoester
  15660. aminoester
  15661. synthesis
  15662. aminofluorosulfurane
  15663. aminoindole
  15664. aminoketone
  15665. aminoketone
  15666. synthesis
  15667. aminomethylation
  15668. aminoorganolithiums
  15669. aminopentadienals
  15670. aminopeptidase
  15671. aminophenylalanine
  15672. aminopyridines
  15673. aminopyridines
  15674. derivatives
  15675. aminopyrimidines
  15676. aminosulfamide
  15677. aminosulfamide
  15678. ligand
  15679. aminotransferase
  15680. aminotransferase
  15681. inhibitor
  15682. aminovinyl
  15683. aminyl
  15684. aminyl
  15685. radical
  15686. cyclization
  15687. pyrrolidine
  15688. sulfenamide
  15689. mercapt
  15690. aminylradicals
  15691. ammelides
  15692. ammelines
  15693. ammonia
  15694. ammonium
  15695. ammonium
  15696. ammonium
  15697. nitrate
  15698. conversion
  15699. amphotericin
  15700. amphotericin
  15701. strategy
  15702. analgesic
  15703. analog
  15704. analogs
  15705. analogue
  15706. analysis
  15707. anchimeric
  15708. anderson
  15709. anderson
  15710. intramolecular
  15711. lewis
  15712. aldehyde
  15713. review
  15714. synth
  15715. angle
  15716. angular
  15717. dride
  15718. anhydrides
  15719. aniline
  15720. aniline
  15721. synthesis
  15722. anilines
  15723. anils
  15724. anion
  15725. anion
  15726. equivalent
  15727. cyclization
  15728. anion
  15729. imine
  15730. ester
  15731. enolate
  15732. addition
  15733. carbonyl
  15734. condensation
  15735. anionic
  15736. anionic
  15737. anionic
  15738. rearrangement
  15739. anionic
  15740. oxy-cope
  15741. rearrangement
  15742. anionotropic
  15743. anionotropic
  15744. rearrangements
  15745. diastereoselective
  15746. addition
  15747. anions
  15748. anisms
  15749. anisomycin
  15750. anisomycin
  15751. nitrogen
  15752. alpha
  15753. annelation
  15754. annellated
  15755. annualtion
  15756. annula
  15757. annulated
  15758. annulated
  15759. furans
  15760. ketones
  15761. cyclization
  15762. annulati
  15763. annulation
  15764. annulation
  15765. anodic
  15766. anodic
  15767. anodic
  15768. oxidation
  15769. alkenylamines
  15770. anomeric
  15771. anomeric
  15772. effect
  15773. anometallics
  15774. ansformations
  15775. antagonist
  15776. antagonists
  15777. anthracene
  15778. anthracene
  15779. isocoumarin
  15780. ortho
  15781. aldehyde
  15782. carbanion
  15783. addition
  15784. anthraceno
  15785. anthracyclinone
  15786. anthracyclinones
  15787. anthraquinones
  15788. anthyridines
  15789. aldol
  15790. aldol
  15791. condensation
  15792. aldol
  15793. reaction
  15794. markovnikov
  15795. addition
  15796. reduction
  15797. anti-13-diol
  15798. anti-13-diol
  15799. ester
  15800. anti-aldol
  15801. anti-felkin
  15802. anti-felkin
  15803. adduct
  15804. antialdol
  15805. antibacterial
  15806. antibacterial
  15807. activity
  15808. penem
  15809. antibiotics
  15810. carbapenem
  15811. antibiotic
  15812. leinamycin
  15813. dioxo
  15814. dithiolane
  15815. moiet
  15816. antibiotics
  15817. antibiotics
  15818. antifungal
  15819. isocoumarins
  15820. hydrangenol
  15821. derivatives
  15822. efficient
  15823. antileukemic
  15824. antimalarial
  15825. antimalarial
  15826. qinghaosu
  15827. antimicrobial
  15828. antimonate
  15829. antimonins
  15830. antimony
  15831. antineoplastic
  15832. antiobiotic
  15833. antiobiotics
  15834. antiopiate
  15835. antiperiplanar
  15836. antisense
  15837. antisense
  15838. oligonucleotides
  15839. antitumor
  15840. antitumor
  15841. agent
  15842. antitumor
  15843. antibiotics
  15844. antitumor
  15845. antibiotics
  15846. esperamicin
  15847. calicheamicin
  15848. gamma
  15849. antitumor
  15850. antibiotics
  15851. kapurimycins
  15852. streptomyces
  15853. aphidicolin
  15854. aplasmomycin
  15855. appen
  15856. append
  15857. appenda
  15858. appenda
  15859. appendag
  15860. appendage
  15861. appendages
  15862. appendages
  15863. application
  15864. applications
  15865. approach
  15866. aprotic
  15867. aqueous
  15868. conditions
  15869. aqueous
  15870. media
  15871. ar-ar
  15872. ar-c-cooh
  15873. ar-cho
  15874. chiral
  15875. sulfoxide
  15876. review
  15877. ligand
  15878. allene
  15879. diels
  15880. alder
  15881. diast
  15882. aranorosin
  15883. arbohydrates
  15884. arborane
  15885. arbring
  15886. arene
  15887. arene
  15888. metal
  15889. complexes
  15890. coordinated
  15891. arenes
  15892. nucleophilic
  15893. arene-metal
  15894. arenes
  15895. arenes
  15896. arenesulfonoxyamine
  15897. arenetricarbonylchro
  15898. arginyl
  15899. aristolactone
  15900. arndt-eistert
  15901. aromatic
  15902. aromatic
  15903. amination
  15904. aromatic
  15905. annulation
  15906. aromatic
  15907. activation
  15908. nitro
  15909. compounds
  15910. carbon
  15911. monoxide
  15912. palladium
  15913. cataly
  15914. aromatic
  15915. nitro
  15916. compounds
  15917. ruthenium
  15918. carbonyl
  15919. nitrobenzene
  15920. aromatic
  15921. organolithium
  15922. aromatic
  15923. organolithium
  15924. aromatic
  15925. polyamides
  15926. carbon
  15927. monoxide
  15928. diamines
  15929. bases
  15930. aromatic
  15931. synthesis
  15932. aromaticity
  15933. aromatics
  15934. aromatics
  15935. functionalization
  15936. electrophilic
  15937. substitution
  15938. aromatization
  15939. around
  15940. aroyl
  15941. arrangement
  15942. arrays/organic-synth
  15943. arrhenius
  15944. arseh
  15945. arsenic
  15946. arsenins
  15947. arser
  15948. arsindoles
  15949. arso2-o-o-so2ar
  15950. arsolanes
  15951. arsolanes
  15952. stibolanes
  15953. arsolene
  15954. arsoles
  15955. stiboles
  15956. bismoles
  15957. arsolene
  15958. arsoles
  15959. arsonium
  15960. artemisinin
  15961. halide
  15962. halides
  15963. iodide
  15964. ketone
  15965. lithium
  15966. lithium
  15967. rearrangement
  15968. lithium
  15969. species
  15970. propargyl
  15971. ethers
  15972. triflate
  15973. triflate
  15974. coupling
  15975. vinyl
  15976. ethers
  15977. aqueous
  15978. solution
  15979. dioxins
  15980. photocyclizatio
  15981. arylalkynes
  15982. arylamine
  15983. arylamines
  15984. arylaminothio
  15985. arylation
  15986. arylation
  15987. arylboronic
  15988. acids
  15989. boronic
  15990. acids
  15991. arylcarbenes
  15992. arylcyclohexyl
  15993. arylglyoxal
  15994. arylidene
  15995. arylidenemalonodinit
  15996. aryllead
  15997. arylnitrenium
  15998. arylnitrenium
  15999. arylocopper
  16000. arylolefins
  16001. arylsulfonoxy
  16002. arylsulfonyloxy
  16003. arylsulphonylhydrazo
  16004. aryne
  16005. arynes
  16006. arynic
  16007. indacene
  16008. subunit
  16009. unsaturated
  16010. ketones
  16011. stereocontrolled
  16012. asokan
  16013. aspartic
  16014. aspartic
  16015. antagonists
  16016. crystal
  16017. structure
  16018. exploration
  16019. aspects
  16020. aspergillus
  16021. aspidosperma
  16022. assemblage
  16023. assignment
  16024. assignments
  16025. assistance
  16026. assists
  16027. astruc
  16028. astruc
  16029. review
  16030. complex
  16031. synthesis
  16032. methodology
  16033. metal
  16034. asymetric
  16035. asymmet
  16036. asymmet
  16037. synthesis
  16038. bryostatin
  16039. asymmetricG
  16040. asymmetric
  16041. asymmetric
  16042. aldol
  16043. reactions
  16044. conjugate
  16045. addition
  16046. carbonyl
  16047. compo
  16048. asymmetric
  16049. alkylation
  16050. asymmetric
  16051. borane
  16052. reduction
  16053. asymmetric
  16054. boration
  16055. asymmetric
  16056. insertion
  16057. asymmetric
  16058. catalyst
  16059. lactone
  16060. asymmetric
  16061. catalytic
  16062. carbomagnesation
  16063. asymmetric
  16064. catalytic
  16065. hydrogenation
  16066. asymmetric
  16067. chiral
  16068. epoxidation
  16069. titanium
  16070. transition
  16071. metal
  16072. asymmetric
  16073. chiral
  16074. stereochem
  16075. aldol
  16076. boron
  16077. borinate
  16078. revie
  16079. asymmetric
  16080. claisen
  16081. rearrangement
  16082. axially
  16083. dissymmetric
  16084. molecu
  16085. asymmetric
  16086. cyclopropanation
  16087. epoxidations
  16088. hydrocarbons
  16089. asymmetric
  16090. asymmetric
  16091. deprotonation
  16092. asymmetric
  16093. diels-alder
  16094. reaction
  16095. asymmetric
  16096. dihydroxylation
  16097. asymmetric
  16098. dihydroxylation
  16099. stereospecific
  16100. synthesis
  16101. allylsil
  16102. asymmetric
  16103. dihyroxylation
  16104. asymmetric
  16105. synthesis
  16106. asymmetric
  16107. asymmetric
  16108. epoxidation
  16109. asymmetric
  16110. epoxidation
  16111. chiral
  16112. auxiliary
  16113. asymmetric
  16114. epoxidation
  16115. eposide
  16116. metal
  16117. nickel
  16118. salen
  16119. review
  16120. asymmetric
  16121. reaction
  16122. chiral
  16123. amino
  16124. phosphine
  16125. decalin
  16126. asymmetric
  16127. hydroformylation
  16128. asymmetric
  16129. hydrogenation
  16130. asymmetric
  16131. hydrogenation
  16132. reaction
  16133. asymmetric
  16134. hydrosilylation
  16135. catalyst
  16136. complexes
  16137. asymmetric
  16138. induction
  16139. asymmetric
  16140. induction
  16141. enantioselective
  16142. addition
  16143. alkyllithi
  16144. asymmetric
  16145. induction
  16146. metal
  16147. salts
  16148. cyclizations
  16149. esters
  16150. nitroal
  16151. asymmetric
  16152. induction
  16153. asymmetric
  16154. lanthanide
  16155. catalyst
  16156. binol
  16157. hydrophosph
  16158. asymmetric
  16159. michael
  16160. addition
  16161. mmetric
  16162. oxidation
  16163. chiral
  16164. sulfoxides
  16165. oxaziridines
  16166. asymmetric
  16167. propargyl
  16168. alcohol
  16169. synthesis
  16170. asymmetric
  16171. protonation
  16172. asymmetric
  16173. radical
  16174. cyclization
  16175. vinyl
  16176. sulfoxide
  16177. tetrahydrofur
  16178. asymmetric
  16179. reduction
  16180. etric
  16181. substitution
  16182. asymmetric
  16183. synthesis
  16184. asymmetric
  16185. synthesis
  16186. anion
  16187. asymmetric
  16188. synthesis
  16189. amino
  16190. acids
  16191. addition
  16192. asymmetric
  16193. synthesis
  16194. antitumor
  16195. activity
  16196. topoisomerase
  16197. asymmetric
  16198. synthesis
  16199. aldehydes
  16200. dialkylzincs
  16201. asymmetric
  16202. synthesis
  16203. bioactive
  16204. peptides
  16205. enkephalin
  16206. asymmetric
  16207. synthesis
  16208. bornanesultam
  16209. asymmetric
  16210. synthesis
  16211. carbon
  16212. asymmetric
  16213. synthesis
  16214. carboxamides
  16215. asymmetric
  16216. synthesis
  16217. cinchona
  16218. alkaloids
  16219. aromatic
  16220. thiols
  16221. asymmetric
  16222. synthesis
  16223. conformational
  16224. analysis
  16225. organic
  16226. compoun
  16227. asymmetric
  16228. synthesis
  16229. esters
  16230. asymmetric
  16231. synthesis
  16232. homoallylic
  16233. alcohols
  16234. carbonyl
  16235. compounds
  16236. asymmetric
  16237. synthesis
  16238. thiol
  16239. esters
  16240. amino
  16241. acids
  16242. lewis
  16243. asymmetric
  16244. synthesis
  16245. trans
  16246. disubstituted
  16247. pyrrolidines
  16248. asymmetric
  16249. synthesis
  16250. vinyl
  16251. sulfoxides
  16252. enantioselective
  16253. synth
  16254. asymmetric
  16255. tandem
  16256. additions
  16257. chiral
  16258. naphthyloxazolines
  16259. naphth
  16260. asymmetric
  16261. thermal
  16262. reactions
  16263. annulation
  16264. reactions
  16265. chiral
  16266. asymmetric
  16267. transmission
  16268. diastereocontrol
  16269. asymmetric
  16270. ullmann
  16271. coupling
  16272. asymmetrically
  16273. asymmetriccyclizatio
  16274. asymmetricorganosila
  16275. complex
  16276. ation
  16277. atkinson
  16278. atkinson
  16279. chiral
  16280. asymmetric
  16281. nitrene
  16282. aziridine
  16283. induction
  16284. amino
  16285. transfer
  16286. transfer
  16287. addition
  16288. electron
  16289. transfer
  16290. processes
  16291. organic
  16292. transfer
  16293. addition
  16294. radical
  16295. additions
  16296. felkin
  16297. transfer
  16298. radical
  16299. chemistry
  16300. atomic
  16301. atoms
  16302. atropisomerism
  16303. attack
  16304. australian
  16305. authors
  16306. authors
  16307. david
  16308. hannessian
  16309. topics
  16310. organotin
  16311. organotin
  16312. authors
  16313. moody
  16314. coates
  16315. topics
  16316. ergot
  16317. alkaloids
  16318. authors
  16319. trost
  16320. topics
  16321. trost
  16322. trost
  16323. review
  16324. allylic
  16325. alkylatio
  16326. authors
  16327. ziegler
  16328. topics
  16329. ziegler
  16330. claisen
  16331. claisen
  16332. rearrangem
  16333. autoinduction
  16334. autoxidation
  16335. auxiliaries
  16336. auxiliaries/cyclo-ad
  16337. auxiliary
  16338. avermectins
  16339. axial
  16340. axially
  16341. axially
  16342. dissymmetric
  16343. molecules
  16344. aluminum
  16345. hydride
  16346. reagents
  16347. mannich
  16348. cyclization
  16349. mannich
  16350. rearrangement
  16351. rearrangements
  16352. wittig
  16353. aza-robinson
  16354. aza-robinson
  16355. annulation
  16356. azaallyl
  16357. azaallylanion
  16358. azaallylanion
  16359. cyclization
  16360. azaannulenes
  16361. azabenzimidazole
  16362. azabicyclic
  16363. azabicyclic
  16364. poison
  16365. opiod
  16366. morphine
  16367. introduction
  16368. banks
  16369. azabicyclo
  16370. azabicyclo
  16371. 5.2.0
  16372. nonanes
  16373. azabicyclo
  16374. 2.2.0
  16375. hexanes
  16376. azabicyclo
  16377. azabutadienes
  16378. azacrown
  16379. azadiene
  16380. azadienes
  16381. azapentadienyl
  16382. azaphenalene
  16383. azaphenalenes
  16384. azaquinolizinium
  16385. azaquinolizinium
  16386. derivatives
  16387. azepine
  16388. azepines
  16389. azete
  16390. azetidinone
  16391. azetine
  16392. azetines
  16393. azide
  16394. ketone
  16395. intramolecular
  16396. wittig
  16397. staudinger
  16398. imine
  16399. azide
  16400. reduction
  16401. azide
  16402. synthesis
  16403. azide
  16404. synthesis
  16405. azide
  16406. thermolysis
  16407. flash
  16408. vacuum
  16409. nitrene
  16410. insertion
  16411. oxazoli
  16412. azide
  16413. azide/copper
  16414. azides
  16415. azido
  16416. azidoiodinanes
  16417. azidonation
  16418. azidosilanes
  16419. azidotriflate
  16420. azine
  16421. azines
  16422. azinohydrazones
  16423. aziridination
  16424. aziridineE
  16425. aziridine
  16426. chiral
  16427. auxiliary
  16428. thermal
  16429. opening
  16430. dipol
  16431. aziridine
  16432. chiral
  16433. ligand
  16434. transition
  16435. metal
  16436. lactam
  16437. cuprate
  16438. aziridine
  16439. cycloaddition
  16440. palladium
  16441. imidazolidinethione
  16442. aziridine
  16443. hydroxy
  16444. amino
  16445. diastereomer
  16446. darzens
  16447. chiral
  16448. aziridine
  16449. radical
  16450. opening
  16451. sonochemistry
  16452. cleavage
  16453. aziridine
  16454. review
  16455. vicinal
  16456. conversion
  16457. sulfite
  16458. azide
  16459. reduc
  16460. aziridine
  16461. review
  16462. preparation
  16463. imine
  16464. silyl
  16465. silicon
  16466. addition
  16467. aziridine
  16468. opening
  16469. aziridine
  16470. opening
  16471. reductive
  16472. cleavage
  16473. radical
  16474. anion
  16475. aziridine
  16476. thermolysis
  16477. electrocyclic
  16478. opening
  16479. azomethine
  16480. aziridinecarboxylic
  16481. aziridines
  16482. aziridinium
  16483. aziridinyl
  16484. aziridinyl
  16485. carbanion
  16486. anion
  16487. reduction
  16488. alkylation
  16489. amino
  16490. azirine
  16491. azirine
  16492. vinyl
  16493. azide
  16494. allene
  16495. photolysis
  16496. matrix
  16497. isolation
  16498. azirines
  16499. azitridines
  16500. azlactone
  16501. azoalkanes
  16502. azocanes
  16503. azocanes
  16504. azocinones
  16505. azocines
  16506. oxocanes
  16507. thiocanes
  16508. oxocanones
  16509. azocine
  16510. azocines
  16511. azocinones
  16512. azodiazo
  16513. azodicarboxylate
  16514. azoelement
  16515. azoles
  16516. azomethine
  16517. azomethine
  16518. ylide
  16519. aziridine
  16520. review
  16521. preparation
  16522. imine
  16523. silyl
  16524. silicon
  16525. addition
  16526. azomethine
  16527. ylide
  16528. carbene
  16529. pyridine
  16530. review
  16531. thiocarbonyl
  16532. ylide
  16533. b-oxoaldimine@
  16534. backvall
  16535. review
  16536. organopalladium
  16537. palladium@
  16538. barium@
  16539. barrett
  16540. silane
  16541. carbanion
  16542. peterson
  16543. olefination
  16544. alkene
  16545. aldehyd@
  16546. induced
  16547. cyclization@
  16548. dipole
  16549. stabilized
  16550. amide
  16551. carbanion
  16552. amine
  16553. chelation
  16554. revie
  16555. beckmann
  16556. rearrangement@
  16557. benzene
  16558. benzocyclobutene@
  16559. benzofuranes@
  16560. benzoxazole
  16561. metalation@
  16562. benzoxazoles
  16563. oxazolones
  16564. oxazolidinones
  16565. oxazolidinediones
  16566. bergman
  16567. cyclization@
  16568. bernasconi
  16569. review
  16570. olefin
  16571. nucleophilic
  16572. addition
  16573. kinetics
  16574. mech@
  16575. ketoester
  16576. imine
  16577. alpha
  16578. unsaturated
  16579. chloride
  16580. dissociation
  16581. energies
  16582. diels
  16583. alder
  16584. reaction
  16585. membered
  16586. borane
  16587. dimethyl
  16588. sulfide@
  16589. boron
  16590. boron
  16591. trifluoride
  16592. etherate
  16593. bridgehead
  16594. radical
  16595. annulation
  16596. synthesis
  16597. cobalt@
  16598. bromobenzaldehydes@
  16599. bt3ch@
  16600. azomethine
  16601. ylide
  16602. carbene
  16603. pyridine
  16604. review
  16605. thiocarbonyl
  16606. ylide
  16607. azomethine
  16608. ylide
  16609. intramolecular
  16610. dipolar
  16611. cycloaddition
  16612. cyclor
  16613. azomethineimines
  16614. azoniaallene
  16615. azonines
  16616. azulenes
  16617. diesters
  16618. hydroxy
  16619. esters
  16620. polyfunctional
  16621. organozinc
  16622. reagents
  16623. ketoesters
  16624. diazo
  16625. ketones
  16626. lactam
  16627. antibiotics
  16628. efficient
  16629. synthesis
  16630. lactam
  16631. antibiotics
  16632. streptomyces
  16633. albus
  16634. directed
  16635. lithiation
  16636. b-cyanoalkene
  16637. b-hydroxy
  16638. b-hydroxy
  16639. ester
  16640. b-hydroxy
  16641. ketone
  16642. b-hydroxy
  16643. sulfone
  16644. b-hydroxy
  16645. sulfoxide
  16646. b-hydroxyketone
  16647. b-hydroxyphosphine
  16648. b-hydroxyphosphine
  16649. oxide
  16650. b-hydroxysulfoxide
  16651. b-keto
  16652. b-keto
  16653. stannanes
  16654. b-keto
  16655. sulfoxide
  16656. b-keto
  16657. sulfoxides
  16658. b-ketoester
  16659. b-ketoester
  16660. unsaturated
  16661. ketone
  16662. b-ketophosphine
  16663. b-ketophosphine
  16664. oxide
  16665. b-ketosulfone
  16666. b-lactam
  16667. b-lactam
  16668. synthesis
  16669. urethane
  16670. b-stannyl
  16671. b-stannyl
  16672. oximes
  16673. b-unsaturated
  16674. baccharin
  16675. backbone
  16676. backcover
  16677. backcover
  16678. review
  16679. alcohol
  16680. deoxygenation
  16681. reduction
  16682. barton
  16683. backlund
  16684. backvall
  16685. backvall
  16686. palladium
  16687. annualtion
  16688. diene
  16689. sulfone
  16690. review
  16691. acetate
  16692. backvall
  16693. review
  16694. organopalladium
  16695. palladium
  16696. baeyer
  16697. baeyer-villiger
  16698. baeyer-villiger
  16699. oxidation
  16700. baird
  16701. baizer
  16702. baizer
  16703. electrochem
  16704. synthesis
  16705. methodology
  16706. carbonyl
  16707. review
  16708. baizer
  16709. electrolysis
  16710. synthesis
  16711. addition
  16712. elimination
  16713. cyclizati
  16714. bakers
  16715. bakers
  16716. yeast
  16717. reduction
  16718. sulfones
  16719. bakmdl
  16720. baldwin
  16721. baldwin
  16722. lactam
  16723. review
  16724. penicillin
  16725. writing
  16726. baldwin
  16727. synthesis
  16728. alkene
  16729. enone
  16730. target
  16731. photocycloaddition
  16732. baldwin's
  16733. bamford
  16734. bamford-stevens
  16735. banks
  16736. barbier
  16737. barbier
  16738. reaction
  16739. barluenga
  16740. barluenga
  16741. diels
  16742. alder
  16743. silicon
  16744. sulfur
  16745. intramolecular
  16746. heterocy
  16747. barrellene
  16748. barrett
  16749. barrett
  16750. review
  16751. chemistry
  16752. thiazoline
  16753. heterocycle
  16754. sulfur
  16755. tauto
  16756. barrett
  16757. review
  16758. nitro
  16759. radical
  16760. cycloaddition
  16761. synthesis
  16762. alkene
  16763. barrett
  16764. silane
  16765. carbanion
  16766. peterson
  16767. olefination
  16768. alkene
  16769. aldehyd
  16770. barrett
  16771. tosylhydrazone
  16772. shapiro
  16773. hydrazone
  16774. vinyl
  16775. carbanio
  16776. barriers
  16777. bartlett
  16778. bartlett
  16779. synthesis
  16780. natural
  16781. product
  16782. stereoselective
  16783. asymmetri
  16784. barton
  16785. barton
  16786. deoxygenation
  16787. catalysis
  16788. aqueous
  16789. solution
  16790. mechanism
  16791. carbocations
  16792. lifet
  16793. catalyzed
  16794. isomerization
  16795. basic
  16796. basic
  16797. medium
  16798. organic
  16799. anions
  16800. catalysis
  16801. basicity
  16802. basis
  16803. bauer
  16804. bauld
  16805. baylis
  16806. baylis
  16807. hillman
  16808. reaction
  16809. aldehydes
  16810. acrylates
  16811. ester
  16812. alpha
  16813. bayliss-hillman
  16814. amide
  16815. carbanion
  16816. organometallic
  16817. alkylation
  16818. dipole
  16819. synthe
  16820. dipole
  16821. stabilized
  16822. amide
  16823. carbanion
  16824. amine
  16825. chelation
  16826. revie
  16827. dipole
  16828. stabilized
  16829. amide
  16830. carbanion
  16831. amine
  16832. chelation
  16833. revie
  16834. metalation
  16835. transition
  16836. state
  16837. theory
  16838. mechanism
  16839. review
  16840. displaceme
  16841. bearing
  16842. becker
  16843. becker
  16844. alkene
  16845. cycloalkene
  16846. ketone
  16847. wittig
  16848. intramolecular
  16849. revie
  16850. becker
  16851. review
  16852. stilbene
  16853. preparation
  16854. alkene
  16855. synthesis
  16856. method
  16857. beckmann
  16858. rearrangement
  16859. begue
  16860. begue
  16861. fluorine
  16862. review
  16863. synthesis
  16864. fluorination
  16865. behavior
  16866. imidazoles
  16867. imidazolines
  16868. imidazolidines
  16869. benneche
  16870. bennett
  16871. bennett
  16872. review
  16873. claisen
  16874. sigmatropic
  16875. rearrangement
  16876. orbital
  16877. bently
  16878. bently
  16879. alkaloid
  16880. review
  16881. synthesis
  16882. phenylethyl
  16883. amine
  16884. isoquinol
  16885. benzaldehyde
  16886. benzaldehydes
  16887. benzamide
  16888. benzamides
  16889. benzannulation
  16890. benzannulation
  16891. vinylketene
  16892. quinone
  16893. carbenoid
  16894. insertion
  16895. carbo
  16896. benzazete
  16897. benzazocin
  16898. benzene
  16899. benzene
  16900. benzene
  16901. dianion
  16902. benzene
  16903. sulfonyl
  16904. allyl
  16905. vinyl
  16906. sulfone
  16907. writing
  16908. introduction
  16909. benzenedisulfonimide
  16910. benzeneselenenyl
  16911. benzeneselenenyl
  16912. triflate
  16913. glycoside
  16914. synthesis
  16915. thioglycosides
  16916. benzeneselenic
  16917. benzeneselenic
  16918. anhydride
  16919. benzenethiol
  16920. benzilic
  16921. benzimidazole
  16922. benzimidazole
  16923. metalation
  16924. benzimidazoles
  16925. benzimidazoles
  16926. imidazolines
  16927. imidazolidines
  16928. benziodoxol
  16929. benzisoxazoles
  16930. benzo
  16931. benzo
  16932. aromatic
  16933. cyclopropene
  16934. preparation
  16935. reactivity
  16936. eliminati
  16937. benzoannulation
  16938. benzoate
  16939. zocyclopropene
  16940. benzocyclopropene
  16941. aromaticity
  16942. carbene
  16943. synthesis
  16944. benzo
  16945. review
  16946. benzodiazepine
  16947. benzodiazepine
  16948. receptor
  16949. antagonist
  16950. methoxy
  16951. methylamides
  16952. benzodiazepines
  16953. benzodioxepin
  16954. benzodioxin
  16955. benzodithiin
  16956. benzofuran
  16957. benzofuran
  16958. synthesis
  16959. benzofuranes
  16960. benzofuranes
  16961. furanones
  16962. benzofurans
  16963. benzofurobenzopyrans
  16964. benzoic
  16965. benzoic
  16966. benzonitrile
  16967. benzopentathiepin
  16968. benzophenanthridines
  16969. benzophenone
  16970. benzopyran
  16971. benzopyran-4-one
  16972. benzopyranes
  16973. benzopyranopyrazole
  16974. benzopyranopyrazolin
  16975. benzopyrans
  16976. benzoquinone
  16977. benzostabase
  16978. benzothiete
  16979. benzothiophenes
  16980. benzothiophenes
  16981. thiophynes
  16982. benzothiopyrans
  16983. benzotr
  16984. benzotr
  16985. azoles
  16986. benzotriazines
  16987. benzotriazol
  16988. benzotriazole
  16989. benzotriazole
  16990. benzotriazolyl
  16991. alkylation
  16992. heteroalkylation
  16993. benzotriazole
  16994. derivatives
  16995. benzotriazole
  16996. nucleophilic
  16997. substitution
  16998. substituted
  16999. benzotri
  17000. benzotriazoles
  17001. benzotriazolyl
  17002. benzotriazolylmethan
  17003. benzoxadithioles
  17004. benzoxazole
  17005. benzoxazoles
  17006. benzoxazoles
  17007. oxazolones
  17008. oxazolidinones
  17009. oxazolidinediones
  17010. benzoxetes
  17011. benzoyl
  17012. benzoyl
  17013. chloride
  17014. benzvalene
  17015. benzyl
  17016. benzyl
  17017. bromide
  17018. benzyl
  17019. ester
  17020. benzyl
  17021. ether
  17022. benzyl
  17023. group
  17024. benzyl
  17025. iodide
  17026. benzyl
  17027. radical
  17028. benzylic
  17029. benzylic
  17030. deprotonation
  17031. benzylic
  17032. lithium
  17033. carbanion
  17034. benzylic
  17035. organolithium
  17036. benzyllithiums
  17037. benzyloxy
  17038. benzyne
  17039. benzyne
  17040. cyclization
  17041. benzynes
  17042. benzynes
  17043. aminobenzotriazoles
  17044. iodosuccinimide
  17045. trapping
  17046. bergman
  17047. bergman
  17048. reaction
  17049. bernasconi
  17050. bernasconi
  17051. review
  17052. olefin
  17053. nucleophilic
  17054. addition
  17055. kinetics
  17056. berson
  17057. berson
  17058. review
  17059. bertrand
  17060. bertrand
  17061. alkene
  17062. radical
  17063. sulfone
  17064. cyclization
  17065. lactam
  17066. pyrro
  17067. bertrand
  17068. beschke
  17069. beschke
  17070. heterocycle
  17071. pyridine
  17072. alkylation
  17073. nitrogen
  17074. oxidation
  17075. bestmann
  17076. bestmann
  17077. wittig
  17078. review
  17079. stereochem
  17080. mechanism
  17081. phosphorous
  17082. amino
  17083. alcohol
  17084. intramolecular
  17085. conjugate
  17086. addition
  17087. vinyl
  17088. amino
  17089. alcohols
  17090. enantioselective
  17091. reduction
  17092. ketones
  17093. boran
  17094. dicarbonyl
  17095. compounds
  17096. triacetates
  17097. aryllead
  17098. fragmentation
  17099. intramolecular
  17100. functionalization
  17101. reagents
  17102. hydroxyphenylsulfone
  17103. desulfonylation
  17104. alkylation
  17105. diiodos
  17106. ketoester
  17107. imine
  17108. alpha
  17109. unsaturated
  17110. chloride
  17111. lactam
  17112. antibiotics
  17113. directed
  17114. aldol
  17115. condensation
  17116. isopenic
  17117. lactam
  17118. antibiotics
  17119. organic
  17120. synthesis
  17121. vinyl
  17122. radicals
  17123. lactams
  17124. lactams
  17125. dihydropyridin
  17126. potassium
  17127. butoxide
  17128. beta-keto
  17129. beta-keto
  17130. ester
  17131. betaine
  17132. bhatt
  17133. bhatt
  17134. ether
  17135. cleavage
  17136. reagent
  17137. review
  17138. silane
  17139. silyl
  17140. silicon
  17141. bianchi
  17142. bianchi
  17143. cycloreversion
  17144. review
  17145. dipole
  17146. dipolar
  17147. azide
  17148. diazo
  17149. bianchi
  17150. retro
  17151. dipolar
  17152. cycloaddition
  17153. review
  17154. cycloreversion
  17155. biaryl
  17156. biaryl
  17157. coupling
  17158. biaryl
  17159. cyanocuprate
  17160. biaryl
  17161. ether
  17162. synthesis
  17163. bicycle
  17164. bicyclic
  17165. bicyclic
  17166. bridge
  17167. alkene
  17168. cycloaddition
  17169. torsion
  17170. review
  17171. bicyclic
  17172. extrusion
  17173. heteroatom
  17174. aromatic
  17175. arene
  17176. preparation
  17177. bicyclic
  17178. ketal
  17179. ether
  17180. cyclic
  17181. review
  17182. enantioselective
  17183. kotsuki
  17184. bicyclic
  17185. lactam
  17186. ngular
  17187. triquinanes
  17188. hydantocidin
  17189. constr
  17190. bicyclization
  17191. bicyclo
  17192. bicyclo
  17193. boron
  17194. silane
  17195. bidentate
  17196. bidentate
  17197. chelation
  17198. biehl
  17199. biehl
  17200. review
  17201. aryne
  17202. cyclization
  17203. target
  17204. synthesis
  17205. benzene
  17206. biehl
  17207. review
  17208. synthesis
  17209. heterocycle
  17210. arylation
  17211. benzyne
  17212. annulat
  17213. bifunctional
  17214. bifunctional
  17215. reagents
  17216. convenient
  17217. synthesis
  17218. selective
  17219. synthes
  17220. biindoles
  17221. bilenes
  17222. billington
  17223. billington
  17224. nickel
  17225. review
  17226. allyl
  17227. metal
  17228. organometallic
  17229. synth
  17230. billups
  17231. bimolecular
  17232. binap
  17233. binap
  17234. catalyst
  17235. binaphthalene
  17236. binaphthol
  17237. binaphthol
  17238. ligand
  17239. binaphthol-triphenyl
  17240. binaphthyls
  17241. binapthol
  17242. binding
  17243. binol
  17244. binol
  17245. titanium
  17246. lewis
  17247. binuclear
  17248. binuclear
  17249. dirhodium
  17250. compounds
  17251. ortho
  17252. metalation
  17253. reactions
  17254. bioactive
  17255. biocatalysis
  17256. biocatalysts
  17257. biochem
  17258. biochemistry
  17259. biochemistry
  17260. genes
  17261. biogenetic
  17262. biogenetic
  17263. synthesis
  17264. indole
  17265. alkaloids
  17266. stereospecific
  17267. biography
  17268. biological
  17269. biological
  17270. activity
  17271. epoxy
  17272. alcohols
  17273. analogs
  17274. nucleos
  17275. biological
  17276. evaluation
  17277. modified
  17278. taxols
  17279. biologically
  17280. biology
  17281. biomimetic
  17282. biomimetic
  17283. alkaloid
  17284. syntheses
  17285. aspidosperma
  17286. alkaloids
  17287. biomimetic
  17288. construction
  17289. skeleton
  17290. biomimetic
  17291. cyclization
  17292. bioorganic
  17293. bioorganic
  17294. chemistry
  17295. biosynthesis
  17296. nsformation
  17297. biotransformation
  17298. enzymes
  17299. enantiogenic
  17300. reactions
  17301. biotransformations
  17302. biotransformations
  17303. biphenyl
  17304. biphenylenes
  17305. biphenylide
  17306. biphosphine
  17307. biradical
  17308. ization
  17309. biradical
  17310. formation
  17311. cleavage
  17312. alkynylcyclobutenone
  17313. biradical
  17314. intermediate
  17315. biradicals
  17316. birch
  17317. birch
  17318. reduction
  17319. 13-di
  17320. p-methoxyphenyl
  17321. 13-propanedionata
  17322. nickel
  17323. 13-di
  17324. p-methoxyphenyl
  17325. 13-propanedionato
  17326. nickel
  17327. 3-methyl-24-pentaned
  17328. nickel
  17329. dipivaloylmethanato
  17330. nickel
  17331. p-allyl
  17332. palladium
  17333. silyl
  17334. ether
  17335. bis-oxazoline
  17336. bisalkylation
  17337. bischler-napieralski
  17338. bischler-napieralski
  17339. cyclization
  17340. biscycloproparene
  17341. bisepoxide
  17342. bishomocubanes
  17343. bishydrazones
  17344. bismins
  17345. bismoles
  17346. bismuth
  17347. bismuth
  17348. bisphosphorous
  17349. bissulfone
  17350. bistelluroalkene
  17351. black
  17352. black
  17353. diazo
  17354. diazomethane
  17355. review
  17356. reagent
  17357. reaction
  17358. black
  17359. heterocycle
  17360. bicyclic
  17361. photochem
  17362. nitrogen
  17363. review
  17364. black
  17365. review
  17366. indole
  17367. electrophilic
  17368. substitution
  17369. biindoles
  17370. blacklund
  17371. bleach
  17372. blechert
  17373. bleomycin
  17374. bleomycins
  17375. block
  17376. blocks
  17377. boche
  17378. review
  17379. dithiane
  17380. lithiate
  17381. anion
  17382. dianion
  17383. sulfone
  17384. carbani
  17385. bodies
  17386. boekelheide
  17387. boekelheide
  17388. cyclophane
  17389. cycloaddition
  17390. synthesis
  17391. methodology
  17392. boger
  17393. boger
  17394. review
  17395. diels
  17396. alder
  17397. azadiene
  17398. nitrogen
  17399. diene
  17400. imine
  17401. boger
  17402. tetrazine
  17403. diels
  17404. alder
  17405. imine
  17406. azadiene
  17407. review
  17408. heterocycl
  17409. boltzmann
  17410. bombyx
  17411. dissociation
  17412. energies
  17413. diels
  17414. alder
  17415. reaction
  17416. membered
  17417. formation
  17418. strengths
  17419. bonded
  17420. bonding
  17421. bonds
  17422. review
  17423. pressure
  17424. cycloaddition
  17425. pressure
  17426. theory
  17427. bop-cl
  17428. bop-cl
  17429. promoted
  17430. macrolactonization
  17431. bopcl
  17432. borabicyclo
  17433. borane
  17434. boration
  17435. borazarofuropyridine
  17436. borepin
  17437. boric
  17438. boric
  17439. borin
  17440. borinate
  17441. borinates
  17442. bornanesultam
  17443. bornic
  17444. borohydride
  17445. borohydride/silica
  17446. borohydrides
  17447. borole
  17448. borole
  17449. borin
  17450. borinates
  17451. borepin
  17452. boron
  17453. boron
  17454. boron
  17455. complex
  17456. enolate
  17457. boron
  17458. enolates
  17459. boron
  17460. hydride
  17461. boron
  17462. hydride
  17463. reduction
  17464. boron
  17465. lewis
  17466. catalyst
  17467. boron
  17468. lewis
  17469. mediated
  17470. opening
  17471. boron
  17472. organoboron
  17473. reduction
  17474. chiral
  17475. asymmetric
  17476. hydroboration
  17477. boron
  17478. reagent
  17479. boron
  17480. stabilized
  17481. carbanion
  17482. boron
  17483. triflouride
  17484. etherate
  17485. boron
  17486. trifluoride
  17487. boron
  17488. trifluoride
  17489. etherate
  17490. boron
  17491. trifluoride
  17492. etherate
  17493. boron-ligand
  17494. boron-ligand
  17495. catalyst
  17496. boronate
  17497. boronates
  17498. boronation
  17499. boronic
  17500. boronic
  17501. boronic
  17502. ester
  17503. botrana
  17504. diazonium
  17505. reactive
  17506. methodology
  17507. alkene
  17508. preparation
  17509. bound
  17510. boykin
  17511. boykin
  17512. review
  17513. spectroscopy
  17514. structure
  17515. organic
  17516. compound
  17517. brain
  17518. braun
  17519. braun
  17520. snieckus
  17521. carbanion
  17522. enolate
  17523. aldol
  17524. stereoselective
  17525. braverman
  17526. breakdown
  17527. bredt
  17528. brefeldin
  17529. breitmaier
  17530. breitmaier
  17531. review
  17532. spectroscopy
  17533. physical
  17534. organic
  17535. hindered
  17536. breslow
  17537. breve
  17538. brevicomin
  17539. brevis
  17540. bridge
  17541. bridged
  17542. bridgehead
  17543. bridgehead
  17544. radical
  17545. annulation
  17546. synthesis
  17547. cobalt
  17548. bridges
  17549. brieger
  17550. brieger
  17551. diels
  17552. alder
  17553. intramolecular
  17554. cycloaddition
  17555. synthesis
  17556. bringmann
  17557. brinkmeyer
  17558. brinkmeyer
  17559. review
  17560. acetal
  17561. formamide
  17562. condensation
  17563. addition
  17564. bristow
  17565. bristow
  17566. reagent
  17567. synthesis
  17568. organometallic
  17569. review
  17570. carbanio
  17571. broadbent
  17572. broadbent
  17573. alkaloid
  17574. spectroscopy
  17575. review
  17576. bromide
  17577. brominated
  17578. bromination
  17579. bromination
  17580. lithium
  17581. enolate
  17582. brominative
  17583. brominative
  17584. cyclizations
  17585. system
  17586. bromine
  17587. bromine
  17588. lithium
  17589. exchange
  17590. bromo
  17591. bromo
  17592. alkyne
  17593. dehydrobromination
  17594. experimental
  17595. method
  17596. bromo
  17597. ester
  17598. reformatsky
  17599. experimental
  17600. synthesis
  17601. fuerstner
  17602. bromoalkyllithium
  17603. bromobenzaldehydes
  17604. bromocyclopropyltrim
  17605. bromoethyl
  17606. bromoethyl
  17607. ester
  17608. bromoethylene
  17609. bromoethylene
  17610. ketone
  17611. bromomethyl
  17612. bromomethylene
  17613. bromonapthhoquinone
  17614. bromostyrene
  17615. bronsted
  17616. brook
  17617. brook
  17618. rearrangement
  17619. brown
  17620. boron
  17621. hydroboration
  17622. review
  17623. reagent
  17624. borane
  17625. brown
  17626. boron
  17627. review
  17628. brown
  17629. hydroboration
  17630. organoborane
  17631. alkene
  17632. brown
  17633. boron
  17634. review
  17635. reduction
  17636. ether
  17637. epoxide
  17638. ketone
  17639. hydroborat
  17640. brown
  17641. crotyl
  17642. borane
  17643. brown
  17644. reduction
  17645. alcohol
  17646. chiral
  17647. borane
  17648. review
  17649. pinene
  17650. brown
  17651. review
  17652. boron
  17653. hydroboration
  17654. stereoselective
  17655. alkyne
  17656. brown
  17657. review
  17658. carbene
  17659. flash
  17660. rearrangement
  17661. ketenes
  17662. extrusion
  17663. brown
  17664. ultrasound
  17665. review
  17666. reference
  17667. hydroboration
  17668. writing
  17669. brownbridge
  17670. brownbridge
  17671. ether
  17672. silicon
  17673. silyl
  17674. review
  17675. chemistry
  17676. brownbridge
  17677. review
  17678. synthesis
  17679. silicon
  17680. reagent
  17681. silyl
  17682. brownbridge
  17683. synthesis
  17684. review
  17685. silicon
  17686. reagent
  17687. silyl
  17688. bryostatin
  17689. bt3ch
  17690. bu3snh
  17691. buchi
  17692. buchwald
  17693. buckminsterfullerene
  17694. buckminsterfullerene
  17695. bufalin
  17696. building
  17697. buivin
  17698. bulgecinine
  17699. bulgecinine
  17700. bulgecinine
  17701. cyclization
  17702. derivatives
  17703. buncel
  17704. isotope
  17705. effect
  17706. kinetics
  17707. theory
  17708. physical
  17709. organic
  17710. organ
  17711. bunnelle
  17712. bunnelle
  17713. ozonolysis
  17714. carbonyl
  17715. oxide
  17716. trioxolane
  17717. review
  17718. burgess
  17719. burgess
  17720. reagent
  17721. burgiI
  17722. burwell
  17723. burwell
  17724. ether
  17725. cleavage
  17726. review
  17727. reagent
  17728. busncl3
  17729. butadiene
  17730. butadienes
  17731. butadienyl
  17732. butadiynyl
  17733. buten
  17734. butenolide
  17735. butenolide
  17736. synthesis
  17737. butenolide
  17738. target
  17739. epoxide
  17740. review
  17741. opening
  17742. cyclization
  17743. butenolides
  17744. butenolides
  17745. seiridium
  17746. cardinale
  17747. reagents
  17748. butenolides
  17749. seiridium
  17750. cardinale
  17751. reagents
  17752. butoxide
  17753. butoxy
  17754. butyl
  17755. tylammonium
  17756. butylbiphenyl
  17757. butyllithium
  17758. butylsulfonyl
  17759. butyrolactone
  17760. butyrolactones
  17761. buynak
  17762. buynak
  17763. allene
  17764. cycloaddition
  17765. review
  17766. preparation
  17767. sulfone
  17768. butenolides
  17769. seiridium
  17770. cardinale
  17771. reagents
  17772. butyl
  17773. lithium@
  17774. coupling
  17775. constants
  17776. carboxylic
  17777. acids
  17778. 1.1.1
  17779. propella@
  17780. reactions
  17781. sigmatropic
  17782. formation
  17783. annulations
  17784. 3-ring
  17785. physical
  17786. organic
  17787. react@
  17788. formation
  17789. annulations
  17790. 5-ring
  17791. diazoketone@
  17792. formation
  17793. annulations
  17794. carbring
  17795. cyclobutanes
  17796. formation
  17797. annulations
  17798. miscellaneous
  17799. indenones
  17800. indan
  17801. formation
  17802. appendag
  17803. enolates
  17804. alkylation@
  17805. formation
  17806. appendages
  17807. 12-addition
  17808. enantiogenic
  17809. react@
  17810. formation
  17811. appendages
  17812. 14-addition
  17813. enantiogenic
  17814. react@
  17815. formation
  17816. appendages
  17817. alkylation
  17818. enolates
  17819. formation
  17820. appendages
  17821. coupling
  17822. organometallics
  17823. formation
  17824. appendages
  17825. enantiogenic
  17826. reactions
  17827. alkylat@
  17828. formation
  17829. appendages
  17830. enantiogenic
  17831. reactions
  17832. organom@
  17833. formation
  17834. appendages
  17835. enolates
  17836. 14-addition
  17837. synthons
  17838. coupling
  17839. constants
  17840. carboxylic
  17841. acids
  17842. 1.1.1
  17843. propella
  17844. chain
  17845. lactams
  17846. chiral
  17847. imine
  17848. organic
  17849. synthesis
  17850. buckminsterfullerene
  17851. adduct
  17852. benzyne
  17853. buckminsterfullerene
  17854. carbon
  17855. glycosides
  17856. glycoside
  17857. rearrangement
  17858. aldehyde
  17859. hydro
  17860. formation
  17861. addition
  17862. elimination
  17863. sequence
  17864. formation
  17865. annulations
  17866. 3-ring
  17867. carbring
  17868. formation
  17869. appendages
  17870. enolates
  17871. c-x-m
  17872. formation
  17873. aromatics
  17874. formation
  17875. phenanthrenes
  17876. formation
  17877. pericyclic
  17878. reactions
  17879. cycloadditions
  17880. formation
  17881. versatile
  17882. cleavage
  17883. derivatives
  17884. hydroxysulfones
  17885. cyclization
  17886. disaccharides
  17887. gylcoside
  17888. insertion
  17889. jasperse
  17890. curran
  17891. fevig
  17892. radical
  17893. review
  17894. fragment
  17895. dimethyl
  17896. acetylenedicarboxyla
  17897. diaza
  17898. c-aryl
  17899. c-aryl
  17900. glycoside
  17901. formation
  17902. annulations
  17903. 5-ring
  17904. formation
  17905. aromatics
  17906. chain
  17907. appendage
  17908. ullmann
  17909. couplin
  17910. formation
  17911. pericyclic
  17912. reactions
  17913. cycloadditions
  17914. formation
  17915. aromatics
  17916. chain
  17917. appendage
  17918. organometallics
  17919. rmation
  17920. appendages
  17921. enantiogenic
  17922. reactions
  17923. alkylat
  17924. rmation
  17925. appendages
  17926. enolates
  17927. enols
  17928. rmation
  17929. pericyclic
  17930. reactions
  17931. sigmatropic
  17932. annul
  17933. ation
  17934. appendages
  17935. enolates
  17936. 12-addition
  17937. annulation
  17938. 6-ring
  17939. format
  17940. pericyclic
  17941. reactions
  17942. sigmatropic
  17943. formati
  17944. annulations
  17945. 5-ring
  17946. formation
  17947. 3-ring
  17948. c-x-m
  17949. silyl
  17950. ethers
  17951. formation
  17952. 5-ring
  17953. appendages
  17954. alkylation
  17955. 12-addition
  17956. formation
  17957. annulation
  17958. 3-ring
  17959. formation
  17960. annulation
  17961. 5-ring
  17962. cyclopentenone
  17963. formation
  17964. annulations
  17965. 14-addition
  17966. annul
  17967. formation
  17968. annulations
  17969. formation
  17970. annulations
  17971. 3-ring
  17972. formation
  17973. annulations
  17974. 3-ring
  17975. 5-ring
  17976. functional
  17977. formation
  17978. annulations
  17979. 3-ring
  17980. carbenoids
  17981. cyclopropan
  17982. formation
  17983. annulations
  17984. 3-ring
  17985. carbring
  17986. cyclop
  17987. formation
  17988. annulations
  17989. 3-ring
  17990. carbring
  17991. cyclopropan
  17992. formation
  17993. annulations
  17994. 3-ring
  17995. ch2i2
  17996. zn-cu
  17997. cyclopropa
  17998. formation
  17999. annulations
  18000. 3-ring
  18001. cycloproparenes
  18002. carbri
  18003. formation
  18004. annulations
  18005. 3-ring
  18006. cyclopropenes
  18007. carbring
  18008. formation
  18009. annulations
  18010. 3-ring
  18011. physical
  18012. organic
  18013. react
  18014. formation
  18015. annulations
  18016. 3-ring
  18017. formation
  18018. annulations
  18019. 3-ring
  18020. stereochemistry
  18021. carben
  18022. formation
  18023. annulations
  18024. 3-ring
  18025. stereochemistry
  18026. carbri
  18027. formation
  18028. annulations
  18029. 4-ring
  18030. formation
  18031. annulations
  18032. 4-ring
  18033. cyclobutene
  18034. carbring
  18035. formation
  18036. annulations
  18037. 4-ring
  18038. cyclopropanes
  18039. cyclopro
  18040. formation
  18041. annulations
  18042. 4-ring
  18043. hetring
  18044. formation
  18045. annulations
  18046. 4-ring
  18047. photochemical
  18048. photoche
  18049. formation
  18050. annulations
  18051. 4-ring
  18052. photochemical
  18053. reaction
  18054. formation
  18055. annulations
  18056. 5-ring
  18057. formation
  18058. annulations
  18059. 5-ring
  18060. 2-cyclopenten-1-ones
  18061. formation
  18062. annulations
  18063. 5-ring
  18064. 6-ring
  18065. formation
  18066. annulations
  18067. 5-ring
  18068. 6-ring
  18069. 7-ring
  18070. meno2
  18071. formation
  18072. annulations
  18073. 5-ring
  18074. 6-ring
  18075. radical
  18076. carbrin
  18077. formation
  18078. annulations
  18079. 5-ring
  18080. cyclopropane
  18081. cleavage
  18082. formation
  18083. annulations
  18084. 5-ring
  18085. diazoketone
  18086. formation
  18087. annulations
  18088. 5-ring
  18089. enones
  18090. nazarov
  18091. cyclisa
  18092. formation
  18093. annulations
  18094. 5-ring
  18095. expansion
  18096. physical
  18097. formation
  18098. annulations
  18099. 5-ring
  18100. furans
  18101. cyclopentenones
  18102. formation
  18103. annulations
  18104. 5-ring
  18105. physical
  18106. organic
  18107. react
  18108. formation
  18109. annulations
  18110. 5-ring
  18111. target
  18112. synthesis
  18113. unnat
  18114. formation
  18115. annulations
  18116. 5-ring
  18117. ylides
  18118. 23-dipolar
  18119. formation
  18120. annulations
  18121. 6-ring
  18122. formation
  18123. annulations
  18124. 6-ring
  18125. alkenes
  18126. annulation
  18127. formation
  18128. annulations
  18129. 6-ring
  18130. formation
  18131. annulations
  18132. 6-ring
  18133. cycloaddition
  18134. formation
  18135. annulations
  18136. 6-ring
  18137. cyclohexenone
  18138. carbring
  18139. formation
  18140. annulations
  18141. 6-ring
  18142. organometallics
  18143. silico
  18144. formation
  18145. annulations
  18146. 6-ring
  18147. robinson
  18148. annelation
  18149. formation
  18150. annulations
  18151. 6-ring
  18152. target
  18153. synthesis
  18154. misce
  18155. formation
  18156. annulations
  18157. carbring
  18158. cyclobutanes
  18159. formation
  18160. annulations
  18161. cycloadditions
  18162. aromatics
  18163. formation
  18164. annulations
  18165. heteroannulations
  18166. miscellaneo
  18167. formation
  18168. annulations
  18169. medium
  18170. alkynes
  18171. cycloalky
  18172. formation
  18173. annulations
  18174. medium
  18175. pericyclic
  18176. reacti
  18177. formation
  18178. annulations
  18179. medium
  18180. osure
  18181. formation
  18182. annulations
  18183. ellaneous
  18184. formation
  18185. annulations
  18186. miscell
  18187. neous
  18188. formation
  18189. annulations
  18190. miscellaneous
  18191. formation
  18192. annulations
  18193. miscellaneous
  18194. 6-ring
  18195. formation
  18196. annulations
  18197. miscellaneous
  18198. allylsilanes
  18199. formation
  18200. annulations
  18201. miscellaneous
  18202. electrochemical
  18203. formation
  18204. annulations
  18205. miscellaneous
  18206. enolates
  18207. annula
  18208. formation
  18209. annulations
  18210. miscellaneous
  18211. enones
  18212. formation
  18213. annulations
  18214. miscellaneous
  18215. functional
  18216. formation
  18217. annulations
  18218. miscellaneous
  18219. indenones
  18220. indan
  18221. formation
  18222. annulations
  18223. miscellaneous
  18224. indenones
  18225. indan
  18226. formation
  18227. annulations
  18228. miscellaneous
  18229. medium
  18230. formation
  18231. annulations
  18232. miscellaneous
  18233. michael
  18234. additio
  18235. formation
  18236. annulations
  18237. miscellaneous
  18238. photochemical
  18239. formation
  18240. annulations
  18241. miscellaneous
  18242. physical
  18243. organi
  18244. formation
  18245. annulations
  18246. miscellaneous
  18247. triterpenoids
  18248. formation
  18249. annulations
  18250. expans
  18251. formation
  18252. annulations
  18253. expansion
  18254. formation
  18255. annulations
  18256. expansion
  18257. contraction
  18258. formation
  18259. annulations
  18260. expansion
  18261. photochemical
  18262. formation
  18263. annulations
  18264. expansion
  18265. physical
  18266. organ
  18267. formation
  18268. annulations
  18269. expansion
  18270. formation
  18271. ndages
  18272. 14-addition
  18273. formation
  18274. append
  18275. enantiogenic
  18276. reactions
  18277. organom
  18278. formation
  18279. appendag
  18280. 12-addition
  18281. formation
  18282. appendag
  18283. 12-addition
  18284. diastereogenic
  18285. formation
  18286. appendag
  18287. enolates
  18288. alkylation
  18289. formation
  18290. appendages
  18291. formation
  18292. appendages
  18293. 12-addit
  18294. x-c-m
  18295. formation
  18296. appendages
  18297. 12-addition
  18298. formation
  18299. appendages
  18300. 12-addition
  18301. aldol
  18302. enantiogenic
  18303. formation
  18304. appendages
  18305. 12-addition
  18306. alkylation
  18307. carboni
  18308. formation
  18309. appendages
  18310. 12-addition
  18311. alkylation
  18312. diaster
  18313. formation
  18314. appendages
  18315. 12-addition
  18316. alkylation
  18317. enolate
  18318. formation
  18319. appendages
  18320. 12-addition
  18321. radical
  18322. additi
  18323. formation
  18324. appendages
  18325. 12-addition
  18326. c-c-m
  18327. formation
  18328. appendages
  18329. 12-addition
  18330. c-c-m
  18331. carbometal
  18332. formation
  18333. appendages
  18334. 12-addition
  18335. c-c-m
  18336. formation
  18337. appendages
  18338. 12-addition
  18339. hydrocarbons
  18340. formation
  18341. appendages
  18342. 12-addition
  18343. carbometallation
  18344. formation
  18345. appendages
  18346. 12-addition
  18347. diastereogenic
  18348. formation
  18349. appendages
  18350. 12-addition
  18351. enantiogenic
  18352. react
  18353. formation
  18354. appendages
  18355. 12-addition
  18356. enolates
  18357. formation
  18358. appendages
  18359. 12-addition
  18360. enolates
  18361. organomet
  18362. formation
  18363. appendages
  18364. 12-addition
  18365. functional
  18366. groups
  18367. formation
  18368. appendages
  18369. 12-addition
  18370. palladium
  18371. formation
  18372. appendages
  18373. 12-addition
  18374. physical
  18375. organic
  18376. formation
  18377. appendages
  18378. 12-addition
  18379. stereochemistry
  18380. formation
  18381. appendages
  18382. 12-addition
  18383. sulphur
  18384. sulfoximin
  18385. formation
  18386. appendages
  18387. 12-additions
  18388. carbometallation
  18389. formation
  18390. appendages
  18391. 14-addition
  18392. formation
  18393. appendages
  18394. 14-addition
  18395. aldehydes
  18396. formation
  18397. appendages
  18398. 14-addition
  18399. formation
  18400. appendages
  18401. 14-addition
  18402. dicarbo
  18403. formation
  18404. appendages
  18405. 14-addition
  18406. diastereogenic
  18407. formation
  18408. appendages
  18409. 14-addition
  18410. tiogenic
  18411. react
  18412. formation
  18413. appendages
  18414. 14-addition
  18415. enantiogenic
  18416. react
  18417. formation
  18418. appendages
  18419. 14-addition
  18420. formation
  18421. appendages
  18422. 14-addition
  18423. ketones
  18424. formation
  18425. appendages
  18426. 14-addition
  18427. organometallics
  18428. formation
  18429. appendages
  18430. 14-addition
  18431. organometallics
  18432. formation
  18433. appendages
  18434. 14-addition
  18435. physical
  18436. organic
  18437. formation
  18438. appendages
  18439. alkylation
  18440. formation
  18441. appendages
  18442. alkylation
  18443. acylation
  18444. 13-dithia
  18445. formation
  18446. appendages
  18447. alkylation
  18448. alkynes
  18449. formation
  18450. appendages
  18451. alkylation
  18452. annulations
  18453. formation
  18454. appendages
  18455. alkylation
  18456. boron
  18457. organometalli
  18458. formation
  18459. appendages
  18460. alkylation
  18461. formation
  18462. appendages
  18463. alkylation
  18464. formation
  18465. appendages
  18466. alkylation
  18467. enantiogenic
  18468. formation
  18469. appendages
  18470. alkylation
  18471. enantiogenic
  18472. reacti
  18473. formation
  18474. appendages
  18475. alkylation
  18476. enolates
  18477. formation
  18478. appendages
  18479. alkylation
  18480. functional
  18481. groups
  18482. formation
  18483. appendages
  18484. alkylation
  18485. c-c-m
  18486. c-x-m
  18487. formation
  18488. appendages
  18489. alkylation
  18490. organometallics
  18491. formation
  18492. appendages
  18493. alkylation
  18494. reagents
  18495. 4-dimethyl
  18496. formation
  18497. appendages
  18498. alkylation
  18499. formation
  18500. appendages
  18501. alkylation
  18502. sigmatropic
  18503. formation
  18504. appendages
  18505. alkylation
  18506. silicon
  18507. formation
  18508. appendages
  18509. coupling
  18510. formation
  18511. appendages
  18512. coupling
  18513. aromatics
  18514. functi
  18515. formation
  18516. appendages
  18517. coupling
  18518. boron
  18519. formation
  18520. appendages
  18521. coupling
  18522. formation
  18523. appendages
  18524. coupling
  18525. electrochemical
  18526. elect
  18527. formation
  18528. appendages
  18529. coupling
  18530. enantiogenic
  18531. reaction
  18532. formation
  18533. appendages
  18534. coupling
  18535. nickel
  18536. palladium
  18537. formation
  18538. appendages
  18539. coupling
  18540. organometallics
  18541. formation
  18542. appendages
  18543. diastereogenic
  18544. react
  18545. 12-ad
  18546. formation
  18547. appendages
  18548. diastereogenic
  18549. reactions
  18550. 12-ad
  18551. formation
  18552. appendages
  18553. diastereogenic
  18554. reactions
  18555. funct
  18556. formation
  18557. appendages
  18558. diastereogenic
  18559. reactions
  18560. physi
  18561. formation
  18562. appendages
  18563. diastereogenic
  18564. reactions
  18565. stere
  18566. formation
  18567. appendages
  18568. electrochemistry
  18569. electrochemic
  18570. formation
  18571. appendages
  18572. lates
  18573. 12-addition
  18574. formation
  18575. appendages
  18576. enantiogenic
  18577. diast
  18578. reogenic
  18579. formation
  18580. appendages
  18581. enantiogenic
  18582. diastereogenic
  18583. formation
  18584. appendages
  18585. enantiogenic
  18586. reactions
  18587. formation
  18588. appendages
  18589. enantiogenic
  18590. reactions
  18591. 12-addi
  18592. formation
  18593. appendages
  18594. enantiogenic
  18595. reactions
  18596. 14-addi
  18597. formation
  18598. appendages
  18599. enantiogenic
  18600. reactions
  18601. acetals
  18602. formation
  18603. appendages
  18604. enantiogenic
  18605. reactions
  18606. alkylat
  18607. formation
  18608. appendages
  18609. enantiogenic
  18610. reactions
  18611. biotran
  18612. formation
  18613. appendages
  18614. enantiogenic
  18615. reactions
  18616. boron
  18617. formation
  18618. appendages
  18619. enantiogenic
  18620. reactions
  18621. boron
  18622. formation
  18623. appendages
  18624. enantiogenic
  18625. reactions
  18626. c-c-m
  18627. formation
  18628. appendages
  18629. enantiogenic
  18630. reactions
  18631. c-c-x
  18632. formation
  18633. appendages
  18634. enantiogenic
  18635. reactions
  18636. c-x-m
  18637. formation
  18638. appendages
  18639. enantiogenic
  18640. reactions
  18641. formation
  18642. appendages
  18643. enantiogenic
  18644. reactions
  18645. formation
  18646. appendages
  18647. enantiogenic
  18648. reactions
  18649. camphor
  18650. formation
  18651. appendages
  18652. enantiogenic
  18653. reactions
  18654. chiral
  18655. formation
  18656. appendages
  18657. enantiogenic
  18658. reactions
  18659. diaster
  18660. formation
  18661. appendages
  18662. enantiogenic
  18663. reactions
  18664. enolate
  18665. formation
  18666. appendages
  18667. enantiogenic
  18668. reactions
  18669. functio
  18670. formation
  18671. appendages
  18672. enantiogenic
  18673. reactions
  18674. organom
  18675. formation
  18676. appendages
  18677. enantiogenic
  18678. reactions
  18679. physica
  18680. formation
  18681. appendages
  18682. enantiogenic
  18683. reactions
  18684. reducti
  18685. formation
  18686. appendages
  18687. enantiogenic
  18688. reactions
  18689. stere
  18690. formation
  18691. appendages
  18692. enantiogenic
  18693. reactions
  18694. stereoc
  18695. formation
  18696. appendages
  18697. enolates
  18698. formation
  18699. appendages
  18700. enolates
  18701. 12-addition
  18702. formation
  18703. appendages
  18704. enolates
  18705. 12-addition
  18706. aldol
  18707. formation
  18708. appendages
  18709. enolates
  18710. 12-addition
  18711. formation
  18712. appendages
  18713. enolates
  18714. 12-addition
  18715. formation
  18716. appendages
  18717. enolates
  18718. 12-addition
  18719. heteroann
  18720. formation
  18721. appendages
  18722. enolates
  18723. 12-addition
  18724. c-c-m
  18725. formation
  18726. appendages
  18727. enolates
  18728. 12-addition
  18729. formation
  18730. appendages
  18731. enolates
  18732. 14-addition
  18733. alkylatio
  18734. formation
  18735. appendages
  18736. enolates
  18737. 14-addition
  18738. synthons
  18739. formation
  18740. appendages
  18741. enolates
  18742. alkylation
  18743. formation
  18744. appendages
  18745. enolates
  18746. alkylation
  18747. 14-additio
  18748. formation
  18749. appendages
  18750. enolates
  18751. alkylation
  18752. enantiogen
  18753. formation
  18754. appendages
  18755. enolates
  18756. c-n-m
  18757. formation
  18758. appendages
  18759. enolates
  18760. c-n-r
  18761. c-n-m
  18762. formation
  18763. appendages
  18764. enolates
  18765. formation
  18766. appendages
  18767. enolates
  18768. enolates
  18769. formation
  18770. appendages
  18771. enolates
  18772. c-x-m
  18773. formation
  18774. appendages
  18775. enolates
  18776. c-x-m
  18777. acids
  18778. formation
  18779. appendages
  18780. enolates
  18781. c-x-m
  18782. alkylati
  18783. formation
  18784. appendages
  18785. enolates
  18786. c-x-m
  18787. formation
  18788. appendages
  18789. enolates
  18790. formation
  18791. appendages
  18792. enolates
  18793. formation
  18794. appendages
  18795. enolates
  18796. formation
  18797. appendages
  18798. enolates
  18799. isocyanid
  18800. formation
  18801. appendages
  18802. enolates
  18803. dicarbonyl
  18804. c-x-m
  18805. formation
  18806. appendages
  18807. enolates
  18808. homoenolates
  18809. synthons
  18810. formation
  18811. appendages
  18812. enolates
  18813. reactions
  18814. knoeve
  18815. formation
  18816. appendages
  18817. enolates
  18818. formation
  18819. appendages
  18820. enolates
  18821. ketones
  18822. alkylat
  18823. formation
  18824. appendages
  18825. enolates
  18826. organometallics
  18827. eleme
  18828. formation
  18829. appendages
  18830. enolates
  18831. oxazines
  18832. thiazines
  18833. formation
  18834. appendages
  18835. enolates
  18836. photochemical
  18837. formation
  18838. appendages
  18839. miscellaneous
  18840. formation
  18841. appendages
  18842. miscellaneous
  18843. 14-addition
  18844. formation
  18845. appendages
  18846. miscellaneous
  18847. reactions
  18848. formation
  18849. appendages
  18850. organometallics
  18851. copper
  18852. oxidati
  18853. formation
  18854. appendages
  18855. organometallics
  18856. lithium
  18857. magnes
  18858. formation
  18859. appendages
  18860. anion
  18861. formation
  18862. appendages
  18863. enolates
  18864. isocyanid@
  18865. formation
  18866. aromatic
  18867. formation@
  18868. formation
  18869. aromatics
  18870. heteroaromatic
  18871. synthesis
  18872. chain
  18873. formation
  18874. aromatics
  18875. formation
  18876. hetring
  18877. coum@
  18878. formation
  18879. aromatics
  18880. functionalisation
  18881. arenes
  18882. formation
  18883. functional
  18884. groups
  18885. preparations
  18886. appendages@
  18887. formation
  18888. heteroannulations
  18889. 5-ring
  18890. 6-ring
  18891. alkenes
  18892. formation
  18893. heteroannulations
  18894. aminoacetals
  18895. heterocycl@
  18896. formation
  18897. yclic
  18898. reactions
  18899. cycloadditions
  18900. formation
  18901. pericyclic
  18902. reactions
  18903. cycloadditions
  18904. formation
  18905. pericyclic
  18906. reactions
  18907. cycloadditions
  18908. formation
  18909. pericyclic
  18910. reactions
  18911. reaction
  18912. formation
  18913. target
  18914. synthesis
  18915. alkaloids
  18916. annulation
  18917. insertion@
  18918. c-nh-no2
  18919. cadmium
  18920. lead@
  18921. caldwell@
  18922. captodative
  18923. carbanion
  18924. formation
  18925. aromatic
  18926. formation
  18927. formation
  18928. aromatics
  18929. chain
  18930. appendage
  18931. formation
  18932. aromatics
  18933. chain
  18934. appendage
  18935. nitro
  18936. formation
  18937. aromatics
  18938. chain
  18939. appendage
  18940. arenes
  18941. ar-ar
  18942. formation
  18943. aromatics
  18944. chain
  18945. appendage
  18946. heteroaromatic
  18947. formation
  18948. aromatics
  18949. chain
  18950. appendage
  18951. reactions
  18952. formation
  18953. aromatics
  18954. chain
  18955. appendage
  18956. organometallics
  18957. formation
  18958. aromatics
  18959. chain
  18960. appendage
  18961. physical
  18962. organi
  18963. formation
  18964. aromatics
  18965. chain
  18966. appendage
  18967. stilbenes
  18968. arene
  18969. formation
  18970. aromatics
  18971. chain
  18972. extension
  18973. formation
  18974. aromatics
  18975. heter
  18976. aromatic
  18977. synthesis
  18978. formation
  18979. aromatics
  18980. heteroaromatic
  18981. synthesis
  18982. formation
  18983. aromatics
  18984. heteroaromatic
  18985. synthesis
  18986. formation
  18987. aromatics
  18988. heteroaromatic
  18989. synthesis
  18990. formation
  18991. aromatics
  18992. heteroaromatic
  18993. synthesis
  18994. chain
  18995. formation
  18996. aromatics
  18997. heteroaromatic
  18998. synthesis
  18999. functi
  19000. formation
  19001. aromatics
  19002. heteroaromatic
  19003. synthesis
  19004. heter
  19005. formation
  19006. aromatics
  19007. heteroaromatic
  19008. synthesis
  19009. hetero
  19010. formation
  19011. aromatics
  19012. heteroaromatic
  19013. synthesis
  19014. hetrin
  19015. formation
  19016. aromatics
  19017. heteroaromatic
  19018. synthesis
  19019. formation
  19020. aromatics
  19021. heteroaromatic
  19022. synthesis
  19023. nenitz
  19024. formation
  19025. aromatics
  19026. heteroaromatic
  19027. synthesis
  19028. ortho-
  19029. formation
  19030. aromatics
  19031. heteroaromatic
  19032. synthesis
  19033. pyrrol
  19034. formation
  19035. aromatics
  19036. nctionalisation
  19037. organome
  19038. formation
  19039. aromatics
  19040. formation
  19041. carbohydrates
  19042. formation
  19043. aromatics
  19044. formation
  19045. carbring
  19046. formation
  19047. aromatics
  19048. formation
  19049. chain
  19050. appendage
  19051. formation
  19052. aromatics
  19053. formation
  19054. diynes
  19055. c-c-c
  19056. formation
  19057. aromatics
  19058. formation
  19059. hetring
  19060. formation
  19061. aromatics
  19062. formation
  19063. organometallics
  19064. formation
  19065. aromatics
  19066. formation
  19067. photochemical
  19068. formation
  19069. aromatics
  19070. formation
  19071. reduction
  19072. annula
  19073. formation
  19074. aromatics
  19075. funct
  19076. onalisation
  19077. formation
  19078. aromatics
  19079. functionalisation
  19080. formation
  19081. aromatics
  19082. functionalisation
  19083. acylatio
  19084. formation
  19085. aromatics
  19086. functionalisation
  19087. annulati
  19088. formation
  19089. aromatics
  19090. functionalisation
  19091. formation
  19092. aromatics
  19093. functionalisation
  19094. formation
  19095. aromatics
  19096. functionalisation
  19097. formation
  19098. aromatics
  19099. functionalisation
  19100. formation
  19101. aromatics
  19102. functionalisation
  19103. arene
  19104. formation
  19105. aromatics
  19106. functionalisation
  19107. arenes
  19108. formation
  19109. aromatics
  19110. functionalisation
  19111. arenes
  19112. formation
  19113. aromatics
  19114. functionalisation
  19115. arenes
  19116. formation
  19117. aromatics
  19118. functionalisation
  19119. arenes
  19120. formation
  19121. aromatics
  19122. functionalisation
  19123. aromatic
  19124. formation
  19125. aromatics
  19126. functionalisation
  19127. arylatio
  19128. formation
  19129. aromatics
  19130. functionalisation
  19131. chain
  19132. formation
  19133. aromatics
  19134. functionalisation
  19135. diazoniu
  19136. formation
  19137. aromatics
  19138. functionalisation
  19139. metallat
  19140. formation
  19141. aromatics
  19142. functionalisation
  19143. formation
  19144. aromatics
  19145. functionalisation
  19146. nitratio
  19147. formation
  19148. aromatics
  19149. functionalisation
  19150. organome
  19151. formation
  19152. aromatics
  19153. functionalisation
  19154. photoche
  19155. formation
  19156. aromatics
  19157. functionalisation
  19158. physical
  19159. formation
  19160. aromatics
  19161. functionalisation
  19162. pyrroles
  19163. formation
  19164. functional
  19165. groups
  19166. preparations
  19167. appendages
  19168. formation
  19169. oannulations
  19170. 4-ring
  19171. formation
  19172. heteroannulations
  19173. 3-ring
  19174. enantiogenic
  19175. formation
  19176. heteroannulations
  19177. 3-ring
  19178. epoxides
  19179. oxirane
  19180. formation
  19181. heteroannulations
  19182. 3-ring
  19183. hetring
  19184. formation
  19185. heteroannulations
  19186. 3-ring
  19187. oxiranes
  19188. epoxide
  19189. formation
  19190. heteroannulations
  19191. 3-ring
  19192. reagents
  19193. t-butyl
  19194. formation
  19195. heteroannulations
  19196. 3-ring
  19197. selenium
  19198. formation
  19199. heteroannulations
  19200. 4-ring
  19201. formation
  19202. heteroannulations
  19203. 4-ring
  19204. carbene
  19205. peroxy
  19206. formation
  19207. heteroannulations
  19208. 4-ring
  19209. lactams
  19210. formation
  19211. heteroannulations
  19212. 4-ring
  19213. stereochemistry
  19214. formation
  19215. heteroannulations
  19216. 5-rin
  19217. pyrrolizine
  19218. formation
  19219. heteroannulations
  19220. 5-ring
  19221. 13-dipolar
  19222. cyclo
  19223. formation
  19224. heteroannulations
  19225. 5-ring
  19226. 6-ring
  19227. 12-additi
  19228. formation
  19229. heteroannulations
  19230. 5-ring
  19231. 6-ring
  19232. alkenes
  19233. formation
  19234. heteroannulations
  19235. 5-ring
  19236. 6-ring
  19237. formation
  19238. heteroannulations
  19239. 5-ring
  19240. alcohols
  19241. formation
  19242. heteroannulations
  19243. 5-ring
  19244. pericyclic
  19245. react
  19246. formation
  19247. heteroannulations
  19248. 5-ring
  19249. pyrollizidine
  19250. formation
  19251. heteroannulations
  19252. 5-ring
  19253. pyrroles
  19254. pyrrole
  19255. formation
  19256. heteroannulations
  19257. 5-ring
  19258. ylides
  19259. ylides
  19260. formation
  19261. heteroannulations
  19262. 6-ring
  19263. azadienes
  19264. diels-
  19265. formation
  19266. heteroannulations
  19267. 6-ring
  19268. azines
  19269. imines
  19270. formation
  19271. heteroannulations
  19272. 6-ring
  19273. cycloadd
  19274. formation
  19275. heteroannulations
  19276. 6-ring
  19277. diels
  19278. alder
  19279. formation
  19280. heteroannulations
  19281. 6-ring
  19282. heterocycles
  19283. formation
  19284. heteroannulations
  19285. 6-ring
  19286. pericyclic
  19287. react
  19288. formation
  19289. heteroannulations
  19290. alpha-alkoxyalkylati
  19291. formation
  19292. heteroannulations
  19293. aminoacetals
  19294. heterocycl
  19295. formation
  19296. heteroannulations
  19297. carbazole
  19298. formation
  19299. heteroannulations
  19300. benzodiazepines
  19301. formation
  19302. heteroannulations
  19303. diphenylamines
  19304. diphenyl
  19305. formation
  19306. heteroannulations
  19307. medium
  19308. cycload
  19309. formation
  19310. heteroannulations
  19311. medium
  19312. hetring
  19313. formation
  19314. heteroannulations
  19315. miscellaneous
  19316. 3-dipol
  19317. formation
  19318. heteroannulations
  19319. miscellaneous
  19320. 3-alkoxya
  19321. formation
  19322. heteroannulations
  19323. miscellaneous
  19324. nitrocomp
  19325. formation
  19326. heteroannulations
  19327. miscellaneous
  19328. organomet
  19329. formation
  19330. heteroannulations
  19331. miscellaneous
  19332. formation
  19333. heteroannulations
  19334. miscellaneous
  19335. ylides
  19336. formation
  19337. heteroannulations
  19338. heterocycle
  19339. formation
  19340. heteroannulations
  19341. pericyclic
  19342. reactions
  19343. formation
  19344. miscellaneous
  19345. organometallics
  19346. silicon
  19347. formation
  19348. yclic
  19349. reactions
  19350. cycloadditions
  19351. formation
  19352. pericyclic
  19353. tions
  19354. cycloadditions
  19355. formation
  19356. pericyclic
  19357. cycloadditions
  19358. formation
  19359. pericyclic
  19360. reactio
  19361. cycloadditions
  19362. formation
  19363. pericyclic
  19364. reactio
  19365. electrocyclic
  19366. reacti
  19367. formation
  19368. pericyclic
  19369. reactions
  19370. allyl
  19371. ester
  19372. rearrang
  19373. formation
  19374. pericyclic
  19375. reactions
  19376. cation
  19377. radicals
  19378. formation
  19379. pericyclic
  19380. reactions
  19381. cycloadd
  19382. tions
  19383. formation
  19384. pericyclic
  19385. reactions
  19386. cycloaddi
  19387. formation
  19388. pericyclic
  19389. reactions
  19390. cycloadditio
  19391. formation
  19392. pericyclic
  19393. reactions
  19394. cycloadditions
  19395. formation
  19396. pericyclic
  19397. reactions
  19398. cycloadditions
  19399. formation
  19400. pericyclic
  19401. reactions
  19402. cycloadditions
  19403. formation
  19404. pericyclic
  19405. reactions
  19406. cycloadditions
  19407. formation
  19408. pericyclic
  19409. reactions
  19410. cycloadditions
  19411. formation
  19412. pericyclic
  19413. reactions
  19414. cycloadditions
  19415. formation
  19416. pericyclic
  19417. reactions
  19418. cycloadditions
  19419. formation
  19420. pericyclic
  19421. reactions
  19422. cycloadditions
  19423. formation
  19424. pericyclic
  19425. reactions
  19426. cycloadditions
  19427. formation
  19428. pericyclic
  19429. reactions
  19430. cycloadditions
  19431. formation
  19432. pericyclic
  19433. reactions
  19434. cycloadditions
  19435. formation
  19436. pericyclic
  19437. reactions
  19438. cycloadditions
  19439. formation
  19440. pericyclic
  19441. reactions
  19442. cycloadditions
  19443. formation
  19444. pericyclic
  19445. reactions
  19446. cycloadditions
  19447. formation
  19448. pericyclic
  19449. reactions
  19450. cycloadditions
  19451. formation
  19452. pericyclic
  19453. reactions
  19454. cycloadditions
  19455. formation
  19456. pericyclic
  19457. reactions
  19458. cycloadditions
  19459. formation
  19460. pericyclic
  19461. reactions
  19462. cycloadditions
  19463. formation
  19464. pericyclic
  19465. reactions
  19466. cycloadditions
  19467. formation
  19468. pericyclic
  19469. reactions
  19470. cycloadditions
  19471. formation
  19472. pericyclic
  19473. reactions
  19474. cycloadditions
  19475. formation
  19476. pericyclic
  19477. reactions
  19478. cycloadditions
  19479. formation
  19480. pericyclic
  19481. reactions
  19482. cycloadditions
  19483. aroma
  19484. formation
  19485. pericyclic
  19486. reactions
  19487. cycloadditions
  19488. formation
  19489. pericyclic
  19490. reactions
  19491. cycloadditions
  19492. formation
  19493. pericyclic
  19494. reactions
  19495. cycloadditions
  19496. formation
  19497. pericyclic
  19498. reactions
  19499. cycloadditions
  19500. formation
  19501. pericyclic
  19502. reactions
  19503. electrocyclc
  19504. reactio
  19505. formation
  19506. pericyclic
  19507. reactions
  19508. electrocyclic
  19509. reacti
  19510. formation
  19511. pericyclic
  19512. reactions
  19513. electrocyclic
  19514. therma
  19515. formation
  19516. pericyclic
  19517. reactions
  19518. reactions
  19519. carbome
  19520. formation
  19521. pericyclic
  19522. reactions
  19523. reaction
  19524. formation
  19525. pericyclic
  19526. reactions
  19527. reaction
  19528. formation
  19529. pericyclic
  19530. reactions
  19531. reaction
  19532. annulat
  19533. formation
  19534. pericyclic
  19535. reactions
  19536. reactions
  19537. formation
  19538. pericyclic
  19539. reactions
  19540. reactions
  19541. annula
  19542. formation
  19543. pericyclic
  19544. reactions
  19545. reaction
  19546. formation
  19547. pericyclic
  19548. reactions
  19549. sigmatraopic
  19550. reactio
  19551. formation
  19552. pericyclic
  19553. reactions
  19554. sigmatropic
  19555. formation
  19556. pericyclic
  19557. reactions
  19558. sigmatropic
  19559. annul
  19560. formation
  19561. pericyclic
  19562. reactions
  19563. sigmatropic
  19564. formation
  19565. pericyclic
  19566. reactions
  19567. sigmatropic
  19568. formation
  19569. pericyclic
  19570. reactions
  19571. sigmatropic
  19572. clais
  19573. formation
  19574. pericyclic
  19575. reactions
  19576. sigmatropic
  19577. heter
  19578. formation
  19579. pericyclic
  19580. reactions
  19581. sigmatropic
  19582. formation
  19583. pericyclic
  19584. reactions
  19585. sigmatropic
  19586. physical
  19587. formation
  19588. pericyclic
  19589. reactions
  19590. stereochemistry
  19591. formation
  19592. target
  19593. synthesis
  19594. alkaloids
  19595. annulation
  19596. formation
  19597. useful
  19598. fragments
  19599. appendages
  19600. diastereogeni
  19601. c-c-ar
  19602. c-c-c
  19603. c-c-c-c
  19604. c-c-c-c-c
  19605. c-c-c-c-c-c
  19606. c-c-c-co
  19607. c-c-c-coor
  19608. c-c-c-m
  19609. c-c-c-x
  19610. c-c-cn
  19611. c-c-coor
  19612. c-c-m
  19613. c-c-oh
  19614. c-c-sir3
  19615. c-c-x
  19616. c-ccl3
  19617. c-ch2-coo-ch2-ch
  19618. c-cho
  19619. c-cooh
  19620. c-glycoside
  19621. c-glycoside
  19622. coupling
  19623. insertion
  19624. reaction
  19625. c-mavacurine
  19626. c-n-m
  19627. c-n-r
  19628. c-nh-no2
  19629. c-nh-no2
  19630. c-nh2
  19631. c-nr2
  19632. c-o-c
  19633. c-o-m
  19634. c-o-n-c
  19635. c-o-r
  19636. c-pr3
  19637. c-x-m
  19638. c-x-r
  19639. c-x-y
  19640. c5me5
  19641. cabri
  19642. cabri
  19643. palladium
  19644. reviews
  19645. ligand
  19646. catalyst
  19647. catalysed
  19648. mecha
  19649. cadmium
  19650. cadmium
  19651. caffeines
  19652. compounds
  19653. systems
  19654. calcheamicin
  19655. calcium
  19656. calculation
  19657. calculation
  19658. equivalents
  19659. calculations
  19660. caldwell
  19661. photochem
  19662. review
  19663. temperature
  19664. physical
  19665. organic
  19666. calibration
  19667. calicheamicin
  19668. calicheamicin
  19669. chromophore
  19670. chemistry
  19671. binding
  19672. antibiotics
  19673. calicheamicin
  19674. esperamicin
  19675. analogs
  19676. antitumor
  19677. antibiotics
  19678. calicheamicinone
  19679. calichemicin
  19680. calix
  19681. calixarene
  19682. calixarenes
  19683. calorimetry
  19684. calyculin
  19685. calyx
  19686. cambie
  19687. cameoI
  19688. camphor
  19689. camphor
  19690. sultam
  19691. camphorsulfonyl
  19692. camphorsulfonyl
  19693. oxaziridine
  19694. camptothecin
  19695. oxidation
  19696. cancer
  19697. canescens
  19698. captodative
  19699. captodative
  19700. capture
  19701. carbalkoxy
  19702. carbalkoxy
  19703. radical
  19704. carbamate
  19705. cyclization
  19706. carbamate
  19707. formation
  19708. carbamate
  19709. hydrolysis
  19710. carbamates
  19711. carbamates
  19712. alpha
  19713. metalation
  19714. alpha
  19715. amino
  19716. anion
  19717. equivalent
  19718. carbametallation
  19719. carbamoylpolyoxamic
  19720. carbanion
  19721. carbanion
  19722. carbapalladation
  19723. carbapenams
  19724. carbapenem
  19725. carbapenem
  19726. antibiotics
  19727. carbapenems
  19728. carbazole
  19729. carbazole-1-carboxyl
  19730. carbazoles
  19731. carbebe
  19732. carbene
  19733. carbene
  19734. carbene
  19735. insertion
  19736. carbene
  19737. carbonyl
  19738. ketone
  19739. review
  19740. carbonyl
  19741. ylide
  19742. diazirine
  19743. carbene
  19744. complex
  19745. panation
  19746. alkylation
  19747. olefins
  19748. carbene
  19749. insertion
  19750. bridgehead
  19751. rearrangement
  19752. bicyclic
  19753. eaton
  19754. carbene
  19755. lactam
  19756. cyclobutane
  19757. cyclopropanation
  19758. extrusion
  19759. nitrog
  19760. carbene
  19761. review
  19762. insertion
  19763. stereospecific
  19764. mechanism
  19765. fisher
  19766. carbene
  19767. vinyl
  19768. diazo
  19769. acetylene
  19770. rearrangement
  19771. trimethylsilyl
  19772. carbenes
  19773. carbenium
  19774. carbenium
  19775. carbenoid
  19776. carbenoid
  19777. mediated
  19778. cyclizations
  19779. carbenoids
  19780. carbenoids
  19781. carbinolamine
  19782. carbinolamine
  19783. tumor
  19784. inhibitors
  19785. antileukemic
  19786. activity
  19787. antineo
  19788. carbinyl
  19789. carbnanion
  19790. alumination
  19791. carboanions
  19792. carbocation
  19793. carbocation
  19794. mediated
  19795. annulation
  19796. carbocation
  19797. review
  19798. reaction
  19799. addition
  19800. mechanism
  19801. rearrangement
  19802. carbocations
  19803. carbocycle
  19804. carbocycles
  19805. carbocyclic
  19806. carbocyclic
  19807. formation
  19808. carbocyclization
  19809. carbodesilylation
  19810. carbodestannylation
  19811. carbodienophiles
  19812. carbodiimide
  19813. carbodiimides
  19814. carboethoxy
  19815. carbohydrate
  19816. carbohydrates
  19817. carbohydrates
  19818. chiral
  19819. synthon
  19820. carbohydrates
  19821. carbohyrate
  19822. carbohyrate
  19823. chemistry
  19824. carbolines
  19825. carbolithiation
  19826. carbomagnesation
  19827. carbomagnesiation
  19828. carbomagnesiation
  19829. kinetic
  19830. resolution
  19831. dihydropyran
  19832. grubbs
  19833. carbometalation
  19834. carbometallation
  19835. carbomethoxy
  19836. carbomycin
  19837. carbon
  19838. carbon
  19839. formation
  19840. dimetallic
  19841. organic
  19842. compounds
  19843. transitio
  19844. carbohydrates
  19845. carbon
  19846. formation
  19847. grignard
  19848. reagents
  19849. polysubstituted
  19850. arom@
  19851. carbonates@
  19852. carbonyl
  19853. carbonyl
  19854. compounds
  19855. enones@
  19856. carbonylnitrone@
  19857. carboxylates@
  19858. carbring
  19859. catalysis
  19860. cyanogen
  19861. enolization
  19862. copper
  19863. complexes@
  19864. catalysis
  19865. catalyst
  19866. lewis
  19867. review
  19868. writing
  19869. diels
  19870. alder
  19871. libf4
  19872. lithium@
  19873. catalytic
  19874. catalytic
  19875. asymmetric
  19876. epoxidation
  19877. acylsilanes
  19878. chemistry@
  19879. catalyzed
  19880. asymmetric
  19881. dihydroxylation@
  19882. cationic
  19883. cyclization@
  19884. cations
  19885. cerium
  19886. alkoxide@
  19887. cf3so2x
  19888. chair@
  19889. rearrangement@
  19890. chelation
  19891. non-chelation
  19892. control@
  19893. chelation
  19894. controlled
  19895. addition
  19896. allyl
  19897. stannane@
  19898. chemistry
  19899. chemistry
  19900. arylidene
  19901. thiotetralones@
  19902. chiral
  19903. chiral
  19904. methoxypyridinium
  19905. salts
  19906. alkylation
  19907. serine@
  19908. cobalt
  19909. mediated
  19910. cyclization
  19911. pauson
  19912. khand
  19913. reaction
  19914. kainic
  19915. complex
  19916. copper
  19917. co-catalyst
  19918. carbon
  19919. formation
  19920. grignard
  19921. reagents
  19922. polysubstituted
  19923. carbon
  19924. formation
  19925. stereospecific
  19926. synthesis
  19927. controlled
  19928. carbon
  19929. dioxide
  19930. carboxylate
  19931. carbon
  19932. dioxide
  19933. simultaneous
  19934. protection
  19935. alternative
  19936. locations
  19937. carbon
  19938. monoxide
  19939. carbon
  19940. monoxide
  19941. carbonylation
  19942. carbon
  19943. monoxide
  19944. carbon
  19945. monoxide
  19946. disulfides
  19947. carbon
  19948. monoxide
  19949. hydrosilane
  19950. carbon
  19951. monoxide
  19952. silylformylation
  19953. hydroformylation
  19954. hydrosilan
  19955. carbon
  19956. tetrachloride
  19957. carbonate
  19958. onates
  19959. allenyl
  19960. halides
  19961. esters
  19962. carbonium
  19963. carbonucleophiles
  19964. carbonyl
  19965. carbonyl
  19966. carbonyl
  19967. addition
  19968. carbonyl
  19969. addition
  19970. reaction
  19971. tivity
  19972. reduction
  19973. carbonyl
  19974. compounds
  19975. convenient
  19976. synthesis
  19977. chelation
  19978. alpha
  19979. carbonyl
  19980. compounds
  19981. stannyl
  19982. anion
  19983. metallic
  19984. me3sisnbu3
  19985. carbonyl
  19986. compounds
  19987. titanium
  19988. carbonyl
  19989. compounds
  19990. transition
  19991. state
  19992. secondary
  19993. enamines
  19994. proto
  19995. carbonyl
  19996. insertion
  19997. carbonyl-carbene
  19998. carbonyl-compounds/c
  19999. carbonylation
  20000. carbonylcyclopropane
  20001. carbonylnitrone
  20002. carbonyls
  20003. carbopalladation
  20004. carbosulfenylation
  20005. carbovir
  20006. carboxamide
  20007. carboxamides
  20008. carboxyl
  20009. carboxyl
  20010. esterification
  20011. ester
  20012. amide
  20013. protection
  20014. review
  20015. carboxylate
  20016. xylates
  20017. carboxylation
  20018. carboxylic
  20019. carboxylic
  20020. carboxylic
  20021. derivatives
  20022. carboxylic
  20023. lithiate
  20024. ortho
  20025. lithiation
  20026. director
  20027. aromatic
  20028. carboxylic
  20029. esters
  20030. carbozirconation
  20031. carbri
  20032. carbrin
  20033. carbring
  20034. carbring
  20035. carbring
  20036. carbyne
  20037. carbynes
  20038. carcinogen
  20039. carcinogen
  20040. arylidenemalonodinit
  20041. metabolites
  20042. carcosilation
  20043. cardillo
  20044. cardillo
  20045. cyclization
  20046. electrophilic
  20047. metal
  20048. review
  20049. stereoselect
  20050. cardinale
  20051. cardioactive
  20052. carnosa
  20053. carotene
  20054. carotenoids
  20055. carrying
  20056. carvone
  20057. cascade
  20058. castanospermine
  20059. castle
  20060. castle
  20061. spectroscopy
  20062. review
  20063. writing
  20064. cataly
  20065. catalysed
  20066. catalysid
  20067. catalysis
  20068. yanogen
  20069. enolization
  20070. copper
  20071. complexes
  20072. catalysis
  20073. catalysis
  20074. catalystG
  20075. catalytic
  20076. catalytic
  20077. catalytic
  20078. reaction
  20079. catalytic
  20080. annulation
  20081. atalytic
  20082. reactions
  20083. organic
  20084. synthesis
  20085. ylide
  20086. formation
  20087. cyclop
  20088. catalyzedH
  20089. catalyzed
  20090. asymmetric
  20091. dihydroxylation
  20092. catalyzed
  20093. reactions
  20094. aldehydes
  20095. catalyzed
  20096. reactions
  20097. cyclopentane
  20098. annulation
  20099. trimethylsil
  20100. catalyzed
  20101. reactions
  20102. catalyzed
  20103. reactions
  20104. organotin
  20105. compounds
  20106. oxazin
  20107. catalyzed
  20108. reconstitutive
  20109. condensation
  20110. carbene
  20111. complexes
  20112. catalzed
  20113. catayst
  20114. catecholborane
  20115. cathepsin
  20116. cathodic
  20117. cation
  20118. cation
  20119. radical
  20120. mechanism
  20121. cation
  20122. review
  20123. carbonium
  20124. novel
  20125. bridgehead
  20126. bicyclic
  20127. inside
  20128. cation
  20129. stabilizing
  20130. group
  20131. cationic
  20132. cationic
  20133. propargyl
  20134. mediated
  20135. cyclization
  20136. polyene
  20137. cyclization
  20138. cationic
  20139. rhodium
  20140. catalyst
  20141. cationic
  20142. rhodium
  20143. complex
  20144. cations
  20145. cations
  20146. caubere
  20147. caubere
  20148. reduction
  20149. carbonyl
  20150. reagent
  20151. review
  20152. hydride
  20153. boron
  20154. protecting
  20155. group
  20156. group
  20157. cc-1065
  20158. cc-c-m
  20159. cc-c-x
  20160. ccl3cho
  20161. addition
  20162. alkene
  20163. cecl3
  20164. center
  20165. centered
  20166. centered
  20167. radicals
  20168. pendant
  20169. nitroxide
  20170. radicals
  20171. electron
  20172. centers
  20173. centre
  20174. cephalosporin
  20175. cephalosporin
  20176. allene
  20177. cuprate
  20178. addition
  20179. displacement
  20180. disulfide
  20181. cephalosporins
  20182. cephalotaxine
  20183. cephem
  20184. cephems
  20185. cephen
  20186. ceric
  20187. cerium
  20188. cerium
  20189. enolate
  20190. cerium
  20191. trichloride
  20192. cesium
  20193. cesium
  20194. fluoride
  20195. cf3so2x
  20196. cf3so2x
  20197. cf3so3h
  20198. cf3so3me
  20199. insertion
  20200. reaction
  20201. ch-ch
  20202. ch-ch2-ocoo-ch
  20203. ch-ch2-ocoo-r
  20204. ch-oh
  20205. ch2-c
  20206. ch2i2
  20207. ch2n2
  20208. chacone
  20209. chaetiacandin
  20210. chain
  20211. chain
  20212. addition
  20213. benzenethiol
  20214. chain
  20215. reactions
  20216. enamines
  20217. chain
  20218. reactions
  20219. organic
  20220. synthesis
  20221. cyclization
  20222. alpha
  20223. mesembra
  20224. chains
  20225. chamigrane
  20226. brominated
  20227. sesquiterpene
  20228. bromomethylene
  20229. alkene
  20230. silicon
  20231. epoxide
  20232. allene
  20233. zwitterion
  20234. silyl
  20235. review
  20236. epoxide
  20237. epoxidation
  20238. allene
  20239. favorski
  20240. silicon
  20241. review
  20242. rearrangement
  20243. silane
  20244. vinyl
  20245. alkylation
  20246. methodology
  20247. review
  20248. synthesis
  20249. channels
  20250. chanon
  20251. chanon
  20252. electron
  20253. transfer
  20254. review
  20255. physical
  20256. organic
  20257. radical
  20258. chapman
  20259. chapman
  20260. wolff
  20261. rearrangement
  20262. diazo
  20263. review
  20264. ketone
  20265. carbene
  20266. characterization
  20267. charette
  20268. charette
  20269. asymmetric
  20270. cyclopropanation
  20271. charge
  20272. chatgilialoglu
  20273. chatgilialoglu
  20274. silane
  20275. reduction
  20276. halide
  20277. radical
  20278. review
  20279. cheap
  20280. cheap
  20281. reagent
  20282. cheeseman
  20283. cheeseman
  20284. heterocycle
  20285. pyrazine
  20286. synthesis
  20287. reaction
  20288. review
  20289. chelate
  20290. chelate
  20291. ligands
  20292. chelating
  20293. chelation
  20294. chelation
  20295. control
  20296. chelation
  20297. control
  20298. chelation
  20299. controlled
  20300. addition
  20301. allyl
  20302. stannane
  20303. chelotropic
  20304. chemical
  20305. chemical
  20306. constituents
  20307. amaryllidaceae
  20308. alkaloids
  20309. tertiary
  20310. chemical
  20311. constituents
  20312. rutaceous
  20313. plants
  20314. alkaloids
  20315. chemical
  20316. diversity
  20317. solid
  20318. phase
  20319. synthesis
  20320. cycloaddition
  20321. chemiexcitation
  20322. chemiluminescence
  20323. chemistry
  20324. chemistry
  20325. otetralones
  20326. chemistry
  20327. dimethyldioxirane
  20328. metabolite
  20329. chemistry
  20330. enantioselectivity
  20331. derivatives
  20332. chemistry
  20333. chemoselective
  20334. chemoselectivity
  20335. childs
  20336. childs
  20337. sigmatropic
  20338. rearrangement
  20339. orbital
  20340. symmetry
  20341. review
  20342. chiralG
  20343. chiral
  20344. chiral
  20345. a-keto
  20346. amide
  20347. chiral
  20348. acetal
  20349. chiral
  20350. acetoxy
  20351. acetals
  20352. chiral
  20353. alcohol
  20354. chiral
  20355. alcohol
  20356. synthesis
  20357. chiral
  20358. aldehyde
  20359. chiral
  20360. alkylation
  20361. chiral
  20362. allyl
  20363. boronate
  20364. chiral
  20365. allyl
  20366. reagent
  20367. chiral
  20368. allylsilane
  20369. chiral
  20370. alpha
  20371. chiral
  20372. alpha
  20373. alkoxy
  20374. facial
  20375. diastereoselectivity
  20376. chela
  20377. chiral
  20378. alpha
  20379. bromo
  20380. acrylate
  20381. amine
  20382. conjugate
  20383. addition
  20384. chiral
  20385. aluminum
  20386. binap
  20387. reagent
  20388. chiral
  20389. amide
  20390. phosphine
  20391. chiral
  20392. amine
  20393. chiral
  20394. amine
  20395. chiral
  20396. amine
  20397. ligand
  20398. chiral
  20399. amine
  20400. synthesis
  20401. chiral
  20402. amino
  20403. auxiliary
  20404. chiral
  20405. ammonia
  20406. equivalent
  20407. conjugate
  20408. addition
  20409. enoates
  20410. chiral
  20411. aniline
  20412. synthesis
  20413. chiral
  20414. auxiliary
  20415. chiral
  20416. auxillary
  20417. chiral
  20418. auxilliary
  20419. camphor
  20420. chiral
  20421. azido
  20422. alcohol
  20423. chiral
  20424. chiral
  20425. biaryl
  20426. synthesis
  20427. chiral
  20428. crotyl
  20429. borane
  20430. chiral
  20431. crotyl
  20432. borane
  20433. brown
  20434. chiral
  20435. crotyl
  20436. silane
  20437. chiral
  20438. cyclopentane
  20439. chiral
  20440. reaction
  20441. chiral
  20442. davis
  20443. reagent
  20444. chiral
  20445. diamine
  20446. chiral
  20447. diamine
  20448. ligand
  20449. chiral
  20450. dienophile
  20451. chiral
  20452. chiral
  20453. olefin
  20454. nitrone
  20455. cycloaddition
  20456. vicinal
  20457. chiral
  20458. synthesis
  20459. chiral
  20460. dioxaborolidine
  20461. catalyst
  20462. chiral
  20463. dipyridyl
  20464. ligand
  20465. chiral
  20466. dirhodium
  20467. catalyst
  20468. chiral
  20469. dirhodium
  20470. carboxamide
  20471. catalyst
  20472. chiral
  20473. crotylsilanes
  20474. addition
  20475. reactions
  20476. chiral
  20477. crotylsilanes
  20478. lewis
  20479. trimethylsilyl
  20480. cyclopenten
  20481. chiral
  20482. enamine
  20483. chiral
  20484. ester
  20485. chiral
  20486. epoxy
  20487. alcohols
  20488. epoxy
  20489. sulfoxides
  20490. cyclic
  20491. sulfates
  20492. chiral
  20493. ester
  20494. enolate
  20495. physicochemical
  20496. properties
  20497. enantioselec
  20498. chiral
  20499. hydroboration
  20500. monoisopinocampheylb
  20501. agent
  20502. chiral
  20503. imide
  20504. chiral
  20505. imine
  20506. chiral
  20507. lewis
  20508. catalyst
  20509. chiral
  20510. lewis
  20511. catalyst
  20512. chiral
  20513. ligand
  20514. chiral
  20515. ligand
  20516. catalyst
  20517. chiral
  20518. ligand
  20519. asymmetric
  20520. catalysis
  20521. chiral
  20522. ligands
  20523. asymmetric
  20524. dihydroxylation
  20525. catalytic
  20526. asymmetr
  20527. chiral
  20528. ligands
  20529. lipase
  20530. hexanediol
  20531. cyclic
  20532. sulfate
  20533. enanti
  20534. chiral
  20535. carbene
  20536. complex
  20537. chiral
  20538. nitrogen
  20539. ligand
  20540. chiral
  20541. nitrone
  20542. cycloaddition
  20543. vicinal
  20544. controller
  20545. chiral
  20546. nitroxide
  20547. catalyst
  20548. chiral
  20549. organoborane
  20550. chiral
  20551. organolithium
  20552. chiral
  20553. organomanganese
  20554. catalyst
  20555. chiral
  20556. organometallic
  20557. complex
  20558. chiral
  20559. oxaziridine
  20560. chiral
  20561. oxaziridine
  20562. review
  20563. oxidation
  20564. reagent
  20565. heterocycle
  20566. chiral
  20567. oxazoline
  20568. chiral
  20569. ligand
  20570. chiral
  20571. palladium
  20572. catalyst
  20573. chiral
  20574. phophine
  20575. ligand
  20576. chiral
  20577. phosphorous
  20578. ligands
  20579. chiral
  20580. piperidine
  20581. chiral
  20582. pyridine
  20583. catalyst
  20584. chiral
  20585. pyridinium
  20586. addition
  20587. chiral
  20588. pyridinium
  20589. salts
  20590. chiral
  20591. pyrrolidine
  20592. chiral
  20593. quaternary
  20594. carbon
  20595. terpene
  20596. diels
  20597. alder
  20598. chiral
  20599. review
  20600. organoborane
  20601. asymmetric
  20602. boron
  20603. pinene
  20604. veeranagh
  20605. chiral
  20606. complex
  20607. chiral
  20608. rhodium
  20609. carbene
  20610. complex
  20611. chiral
  20612. ruthenium
  20613. catalyst
  20614. chiral
  20615. secondary
  20616. alcohol
  20617. chiral
  20618. silyl
  20619. cyanation
  20620. chiral
  20621. silyoxystannane
  20622. chiral
  20623. sulfoxide
  20624. chiral
  20625. synthesis
  20626. chiral
  20627. tartarate
  20628. ligand
  20629. chiral
  20630. catalyst
  20631. chiral
  20632. titanium
  20633. catalyst
  20634. chiral
  20635. titanium
  20636. complex
  20637. stereochemic
  20638. chiral
  20639. reagent
  20640. chirality
  20641. chiron
  20642. chirons
  20643. chirons
  20644. arbohydrates
  20645. sugars
  20646. chloral
  20647. chloramine
  20648. chloride
  20649. chloride
  20650. ation
  20651. chlorinations
  20652. chlorite
  20653. chloro
  20654. chloro
  20655. acetate
  20656. chloro
  20657. amide
  20658. chloro
  20659. h5-cyclopentadienyl
  20660. titanium
  20661. chloroacetic
  20662. chloroaldimines
  20663. chlorobenzene
  20664. chlorocarboxylate
  20665. chlorochromate
  20666. chlorohydrins
  20667. chloroiodine
  20668. chloroketone
  20669. chloromagnesium
  20670. chloromethyl
  20671. chloromethylpropene
  20672. chloronitroso
  20673. chloropropenyl
  20674. chlorosulfides
  20675. chlorosulfite
  20676. chlorosulfite
  20677. ester
  20678. chlorosulfonyl
  20679. chlorotrimethylsilan
  20680. chlorovinyl
  20681. chlorovinyl
  20682. alcohol
  20683. chong
  20684. christl
  20685. christl
  20686. benzvalene
  20687. review
  20688. carbanion
  20689. carbene
  20690. novel
  20691. strained
  20692. christl
  20693. synthesis
  20694. spectroscopy
  20695. photorearrangement
  20696. benzvalene
  20697. chromanones
  20698. chromanones
  20699. chromatography
  20700. chromenes
  20701. chromenone
  20702. chromia
  20703. chromia
  20704. pillared
  20705. montmorillonite
  20706. catalyst
  20707. chromium
  20708. chromium
  20709. promoted
  20710. cycloaddition
  20711. chromium
  20712. acetate
  20713. chromium
  20714. amino
  20715. carbene
  20716. complex
  20717. chromium
  20718. carbene
  20719. complex
  20720. chromium
  20721. carbene
  20722. complexes
  20723. chromium
  20724. carbene
  20725. complexes
  20726. alkynes
  20727. ligands
  20728. annulation
  20729. skelet
  20730. chromium
  20731. carbonyl
  20732. complex
  20733. chromium
  20734. chloride
  20735. chromium
  20736. chloride
  20737. catalyst
  20738. chromium
  20739. salen
  20740. complex
  20741. chromium
  20742. tricarbonyl
  20743. complexes
  20744. sulfinyl
  20745. controlled
  20746. formation
  20747. chromium
  20748. trioxide
  20749. oxidation
  20750. chromone
  20751. chromones
  20752. chromophore
  20753. chromophores
  20754. chrysanthemic
  20755. cieplak
  20756. ciguatoxin
  20757. cinchona
  20758. cinchona
  20759. alkaloid
  20760. cinchonda
  20761. alkaloids
  20762. cinnolines
  20763. cinnolines
  20764. phthalazines
  20765. cinnolinium
  20766. cirillo
  20767. divinyl
  20768. epoxides
  20769. rearrangement
  20770. sativenediol
  20771. cispentacin
  20772. cited
  20773. citrus
  20774. citrus
  20775. mealybug
  20776. civet
  20777. claisen
  20778. claisen
  20779. claisen
  20780. transition
  20781. metal
  20782. catalyst
  20783. introduction
  20784. writing
  20785. claisen
  20786. rearrangement
  20787. claisen
  20788. rearrangement
  20789. demethoxydaunomycino
  20790. hydroxyanthraqu
  20791. claisen
  20792. rearrangement
  20793. chelation
  20794. magnesium
  20795. enolate
  20796. claisen
  20797. rearrangement
  20798. claisen
  20799. rearrangement
  20800. demethylsuberosin
  20801. derivatives
  20802. cyclizat
  20803. claisen
  20804. rearrangement
  20805. organic
  20806. synthesis
  20807. stereochemistry
  20808. claisen
  20809. rearrangement
  20810. stereospecific
  20811. synthesis
  20812. vinyl
  20813. ethers
  20814. claramunt
  20815. clark
  20816. clark
  20817. review
  20818. indole
  20819. synthesis
  20820. nitro
  20821. reduction
  20822. enamine
  20823. clathrate
  20824. cleava
  20825. cleavage
  20826. cleavage
  20827. cleavage
  20828. cleavage
  20829. ester
  20830. ether
  20831. conversion
  20832. silicon
  20833. review
  20834. reagent
  20835. trime
  20836. cleavage
  20837. reactions
  20838. organic
  20839. synthesis
  20840. aluminum
  20841. hydride
  20842. cleavage
  20843. subunit
  20844. route
  20845. cleaving
  20846. clelate
  20847. clelate
  20848. griganrd
  20849. addition
  20850. clemmensen
  20851. clezy
  20852. clitocybe
  20853. clive
  20854. clive
  20855. review
  20856. selenium
  20857. umpolung
  20858. methodology
  20859. alkylation
  20860. epoxid
  20861. clock
  20862. clocks
  20863. closing
  20864. closure
  20865. 1.5-hexadiynes
  20866. alkynes
  20867. acetylenes
  20868. alkenes
  20869. cyclotrimerization
  20870. al2o3
  20871. hydrodesulfurization
  20872. catalysts
  20873. co-catalyst
  20874. coates
  20875. cobalt
  20876. cobalt
  20877. catalyzed
  20878. cycloaddition
  20879. cobalt
  20880. alkyne
  20881. complex
  20882. cobalt
  20883. aziridines
  20884. cobalt
  20885. chemistry
  20886. cobalt
  20887. complex
  20888. cobalt
  20889. cyclization
  20890. cobalt
  20891. hexacarbonyl
  20892. cobalt
  20893. hexacarbonyl
  20894. alkyne
  20895. complex
  20896. cobalt
  20897. hydride
  20898. cobalt
  20899. mediated
  20900. annulation
  20901. cobalt
  20902. mediated
  20903. cyclization
  20904. enantioselective
  20905. synthesis
  20906. clito
  20907. cobalt
  20908. mediated
  20909. cyclization
  20910. pauson
  20911. khand
  20912. reaction
  20913. kainic
  20914. cobalt
  20915. nucleophiles
  20916. complexes
  20917. cobalt
  20918. protected
  20919. acetylene
  20920. cockroach
  20921. cockroach
  20922. pheromone
  20923. american
  20924. cockroach
  20925. crassin
  20926. rearrange
  20927. cocl2
  20928. cohen
  20929. cohen
  20930. lithiate
  20931. sulfur
  20932. thiophenyl
  20933. electron
  20934. transfer
  20935. collum
  20936. collum
  20937. tmeda
  20938. diamine
  20939. organolithium
  20940. ligand
  20941. review
  20942. column
  20943. colvin
  20944. colvin
  20945. silicon
  20946. silane
  20947. vinyl
  20948. methodology
  20949. review
  20950. reagent
  20951. combier
  20952. combination
  20953. combined
  20954. comins
  20955. comins
  20956. ortho
  20957. protection
  20958. amine
  20959. carbanion
  20960. alkylation
  20961. review
  20962. common
  20963. common
  20964. chiral
  20965. synthon
  20966. enantiomers
  20967. alkaloids
  20968. indolizidines
  20969. compactin
  20970. compared
  20971. competition
  20972. complementary
  20973. complex
  20974. complex
  20975. complexes
  20976. complexes
  20977. dimerization
  20978. complexes
  20979. hydrogenation
  20980. compo
  20981. composition
  20982. compoumds
  20983. compound
  20984. compouns
  20985. compunds
  20986. computational
  20987. computational
  20988. chemistry
  20989. computational
  20990. study
  20991. computerI
  20992. concerted
  20993. concise
  20994. condenation
  20995. condensation
  20996. condensations
  20997. condensed
  20998. conditions
  20999. conditions/aldol
  21000. conduramine
  21001. configuration
  21002. configurational
  21003. conformation
  21004. conformational
  21005. conformational
  21006. control
  21007. coupling
  21008. constant
  21009. conformational-analy
  21010. conformationally
  21011. conformations
  21012. congested
  21013. conia
  21014. conia
  21015. review
  21016. cyclobutane
  21017. cyclopropane
  21018. rearrangement
  21019. catalyst
  21020. conjugate
  21021. conjugate
  21022. addition
  21023. conjugate
  21024. addition
  21025. cuprate
  21026. copper
  21027. review
  21028. catalyzed
  21029. reagent
  21030. conjugate
  21031. addition
  21032. michael
  21033. addition
  21034. addition
  21035. sulfone
  21036. anion
  21037. conjugate
  21038. addition
  21039. organocopper
  21040. reagents
  21041. acetonides
  21042. conjugate
  21043. addition
  21044. reactions
  21045. conjugate
  21046. addition/cyclization
  21047. conjugate
  21048. addtion
  21049. conjugate
  21050. alkylation
  21051. trimethylaluminium
  21052. copper
  21053. catalysis
  21054. conjugate
  21055. enone
  21056. preparation
  21057. succinimide
  21058. review
  21059. imide
  21060. alkylat
  21061. conjugated
  21062. conjugation
  21063. connection
  21064. constant
  21065. constants
  21066. constituent
  21067. constituents
  21068. constraints
  21069. construction
  21070. construction
  21071. organocopper
  21072. contacts
  21073. containing
  21074. containing
  21075. cyclic
  21076. amide
  21077. hydrogen
  21078. transfer
  21079. complexes
  21080. containing
  21081. natural
  21082. products
  21083. polypropionate
  21084. fragments
  21085. contraction
  21086. contrapolarization
  21087. control
  21088. controller
  21089. convenient
  21090. convenient
  21091. synthesis
  21092. carbomethoxy
  21093. butadiene
  21094. precursor
  21095. convenient
  21096. synthesis
  21097. aromatic
  21098. compounds
  21099. convenient
  21100. synthesis
  21101. esters
  21102. convenient
  21103. synthesis
  21104. convergent
  21105. conversion
  21106. converted
  21107. converted
  21108. synthesis
  21109. azine
  21110. heterocycle
  21111. review
  21112. azaphenalene
  21113. aromati
  21114. coordinated
  21115. coordination
  21116. rearrangement
  21117. copolymerization
  21118. copper
  21119. copper
  21120. carbene
  21121. complex
  21122. copper
  21123. catalyst
  21124. copper
  21125. chloride
  21126. copper
  21127. acetylacetonate/mono
  21128. peroxydicarbonates
  21129. copper
  21130. catalyzed
  21131. cyclopropane
  21132. copper
  21133. chloride
  21134. cucl2
  21135. copper
  21136. co-catalyst
  21137. copper
  21138. mediated
  21139. contraction
  21140. copper
  21141. oxazoline
  21142. copper
  21143. pivalate
  21144. copper
  21145. iodide
  21146. copper
  21147. reagents
  21148. chemistry
  21149. copper
  21150. rhodium
  21151. carbene
  21152. copper-zinc
  21153. corey
  21154. corey
  21155. reduction
  21156. corey
  21157. nitro
  21158. enone
  21159. ketone
  21160. review
  21161. nitration
  21162. preparation
  21163. method
  21164. corey
  21165. oxazaborolidine
  21166. chiral
  21167. reduction
  21168. corey's
  21169. correlation
  21170. corresponding
  21171. corresponding
  21172. alkenes
  21173. convenient
  21174. conversion
  21175. hydroboration
  21176. corrin
  21177. cortisone
  21178. corvergine
  21179. cossu
  21180. coulping
  21181. coumarin
  21182. coumarin
  21183. derivatives
  21184. thiazolyl
  21185. coumarin
  21186. palladium
  21187. catalysis
  21188. cyclization
  21189. oxidative
  21190. addition
  21191. coumarins
  21192. copper
  21193. acetylacetonate/mono
  21194. peroxydicarbonates@
  21195. copper
  21196. iodide
  21197. catalyst@
  21198. coumarins
  21199. coupling
  21200. coupling
  21201. reaction
  21202. binaphthyls
  21203. resolution@
  21204. eophilic
  21205. attack
  21206. olefins@
  21207. cyclization
  21208. cycloaddition
  21209. cycloaddition
  21210. nitro
  21211. phenyl
  21212. benzopyrans
  21213. benzopyranop@
  21214. cycloadditions
  21215. cyclobutanones
  21216. cyclooctatriene
  21217. cyclopentenones@
  21218. cyclopropane
  21219. opening@
  21220. cyclopropenone
  21221. ketals
  21222. diels
  21223. alder
  21224. cyclopropene
  21225. target
  21226. tropol
  21227. threo
  21228. sphingosine
  21229. stereoselective
  21230. synthesis
  21231. serine@
  21232. dazodiazaphosphorine
  21233. dehydrogenation
  21234. deprotection
  21235. derivatives
  21236. dethioacetalization@
  21237. diastereofacial
  21238. selectivity
  21239. asymmetric
  21240. synthesis
  21241. design@
  21242. diazaanthracenes@
  21243. diazo
  21244. aldehyde
  21245. reduction
  21246. lithiate
  21247. ester
  21248. carbanion
  21249. condensati@
  21250. diazo
  21251. imide@
  21252. diazocarbonyl
  21253. dichloromethyl@
  21254. diels
  21255. alder
  21256. approach
  21257. functionalized
  21258. hydroisoquinolines
  21259. coumarins
  21260. coumarins
  21261. palladium
  21262. catalysis
  21263. carbon
  21264. monoxide
  21265. complexes
  21266. counterattack
  21267. couple
  21268. coupling
  21269. coupling
  21270. coutts
  21271. review
  21272. hydroxyl
  21273. amine
  21274. cyclic
  21275. cover
  21276. coxon
  21277. coxon
  21278. felkin
  21279. karabatsos
  21280. review
  21281. model
  21282. carbonyl
  21283. cozzi
  21284. cp2hfcl2
  21285. cp2tich2
  21286. cpmlex
  21287. crabtree's
  21288. crabtree's
  21289. catalyst
  21290. craft
  21291. crafts
  21292. cramI
  21293. chiral
  21294. induction
  21295. addition
  21296. asymmetric
  21297. carbonyl
  21298. felkin
  21299. model
  21300. cram's
  21301. crandall
  21302. crassin
  21303. crcl2
  21304. crcl2
  21305. creary
  21306. crich
  21307. crimmins
  21308. crimmins
  21309. conjugate
  21310. addition
  21311. enolate
  21312. alkyne
  21313. ester
  21314. crimmins
  21315. review
  21316. photochem
  21317. intramolecular
  21318. cycloaddition
  21319. enone
  21320. croconate
  21321. crolactonisation
  21322. cross
  21323. cross
  21324. coupling
  21325. cross
  21326. coupling
  21327. reaction
  21328. alkyl
  21329. grignard
  21330. reagents
  21331. alkyl
  21332. cross
  21333. coupling
  21334. reaction
  21335. australian
  21336. marine
  21337. sponge
  21338. organo
  21339. cross
  21340. coupling
  21341. reaction
  21342. boronic
  21343. acids
  21344. derivatives
  21345. organostan
  21346. cross
  21347. coupling
  21348. reaction
  21349. organic
  21350. electrophiles
  21351. organotin
  21352. cross
  21353. coupling
  21354. reaction
  21355. organomagnesium
  21356. compounds
  21357. grignard
  21358. crotanecine
  21359. crotonate
  21360. crotyl
  21361. omium
  21362. reagent
  21363. crotylation
  21364. crotylboronate
  21365. crotylboronates
  21366. crotyldiisopinocamph
  21367. crotylmetal
  21368. crotylsilanes
  21369. crown
  21370. crown
  21371. crown
  21372. phase
  21373. transfer
  21374. alkylation
  21375. elimination
  21376. reduction
  21377. chelat
  21378. crown
  21379. synthesis
  21380. selectivity
  21381. complex
  21382. phase
  21383. transfer
  21384. catalyst
  21385. crystal
  21386. crystal
  21387. structure
  21388. crystal
  21389. structure
  21390. catalyzed
  21391. crystal
  21392. structure
  21393. complexes
  21394. c5me5
  21395. organolanthanide
  21396. crystal
  21397. structure
  21398. tetraacetylethylene
  21399. furofurans
  21400. crystal-structure
  21401. crystalline
  21402. crystallographic
  21403. crystallographic
  21404. characterization
  21405. crystals
  21406. crystals
  21407. diazide
  21408. pairs
  21409. ctions
  21410. cubane
  21411. cubanes
  21412. cubyl
  21413. cucl2
  21414. cuevas
  21415. cumulated
  21416. cumulenes
  21417. cuneane
  21418. cuprametallation
  21419. cuprate
  21420. addition
  21421. cuprate
  21422. chemistry
  21423. cuprate
  21424. organocopper
  21425. grignard
  21426. addition
  21427. cuprate
  21428. reaction
  21429. cuprates
  21430. cuprates
  21431. organo
  21432. metallic
  21433. enynes
  21434. acceptor
  21435. substituted
  21436. additio
  21437. cupration
  21438. curran
  21439. curran
  21440. radical
  21441. review
  21442. curran
  21443. review
  21444. samarium
  21445. diiodide
  21446. barbier
  21447. radical
  21448. cycliza
  21449. curtin
  21450. curtius
  21451. curtius
  21452. reaction
  21453. cyanamidium
  21454. cyanates
  21455. cyanation
  21456. cyanic
  21457. cyanide
  21458. cyano
  21459. cyano
  21460. cuprate
  21461. cyanoacetamide
  21462. cyanoacetic
  21463. cyanoborates
  21464. cyanoborohydride
  21465. cyanocarbon
  21466. cyanocuprate
  21467. cyanoesters
  21468. cyanogen
  21469. cyanohydrin
  21470. cyanohydrin
  21471. anion
  21472. cyanohydrin
  21473. anion
  21474. alkylation
  21475. cyanohydrins
  21476. cyanoketene
  21477. cyanoketenes
  21478. cyanosilylation
  21479. cyanotrimethylsilane
  21480. cyanurates
  21481. cyanuric
  21482. cyclase
  21483. cyclazidines
  21484. cyclazines
  21485. cycle
  21486. cycles
  21487. cyclialkylation
  21488. cyclialkylations
  21489. cyclic
  21490. onium
  21491. cyclic
  21492. polysulfides
  21493. benzopentathiepin
  21494. varacin
  21495. sulfur
  21496. cyclic
  21497. sulfate
  21498. enolate
  21499. ketone
  21500. ester
  21501. amide
  21502. nitrile
  21503. lactone
  21504. cyclic
  21505. sulfates
  21506. cyclic
  21507. sulfates
  21508. nucleophilic
  21509. attack
  21510. olefins
  21511. cyclic
  21512. sulfones
  21513. cyclipropanes
  21514. cyclisation
  21515. cyclisation
  21516. cyclisations
  21517. cyclitol
  21518. cyclization
  21519. cyclization
  21520. cyclization
  21521. cyclize
  21522. cyclo
  21523. cyclo
  21524. addition
  21525. reactions
  21526. delocalized
  21527. singlet
  21528. vinylcarbenes
  21529. cyclo
  21530. additions
  21531. dipolar
  21532. cycloaddition
  21533. carbocyclic
  21534. compoun
  21535. cyclo-addition/tolue
  21536. cycloadd
  21537. cycloaddi
  21538. cycloadditio
  21539. cycloaddition
  21540. cycloaddition
  21541. cycloaddition
  21542. nitro
  21543. phenyl
  21544. benzopyrans
  21545. benzopyranop
  21546. cycloaddition
  21547. allyl
  21548. cation
  21549. review
  21550. lewis
  21551. chloride
  21552. cycloaddition
  21553. cycloaddition
  21554. elimination
  21555. reactions
  21556. bonded
  21557. participat
  21558. cycloaddition
  21559. enamines
  21560. azide
  21561. triazoline
  21562. retro
  21563. cycloreversion
  21564. cycloaddition
  21565. photochemistry
  21566. cycloaddition
  21567. reaction
  21568. transfer
  21569. cycloaddition
  21570. reactions
  21571. ketenes
  21572. diazabutadienes
  21573. cycloaddition
  21574. reactions
  21575. thermal
  21576. isomerization
  21577. transform
  21578. cycloaddition
  21579. regiochemistry
  21580. diaryl
  21581. nitrilimines
  21582. stereochemi
  21583. cycloaddition
  21584. urrutia
  21585. cycloadditions
  21586. cycloadditions
  21587. cycloadditions
  21588. acylamino
  21589. dienes
  21590. cycloadditions
  21591. gymnomitrol
  21592. sativene
  21593. cycloadditions
  21594. perchlorobutenyne
  21595. ynamines
  21596. cycloadditions
  21597. steric
  21598. control
  21599. cycloadditions
  21600. thiochalcones
  21601. thioketones
  21602. cycloaddtion
  21603. cycloalkane
  21604. cycloalkane
  21605. dione
  21606. ester
  21607. cyclopentenone
  21608. oxidative
  21609. cycloalkanones
  21610. cycloalkene
  21611. cycloalkenes
  21612. cycloalkylation
  21613. cycloalkynes
  21614. cycloaromatization
  21615. lobutadiene
  21616. cyclobutane
  21617. cyclobutane
  21618. synthesis
  21619. cyclobutanes
  21620. cyclobutanol
  21621. cyclobutanone
  21622. cyclobutanone
  21623. synthesis
  21624. cyclobutanones
  21625. cyclobutanones
  21626. cyclobutene
  21627. cyclobutene
  21628. oxides
  21629. cyclohexene
  21630. oxides
  21631. cyclopentene
  21632. oxides
  21633. cyclobutenediones
  21634. cyclobuteneone
  21635. cyclobutenone
  21636. cyclobutenones
  21637. cyclobutenyl
  21638. cyclocarbonylation
  21639. cyclocondensation
  21640. cyclodehydration
  21641. cyclodextrin
  21642. cyclodextrins
  21643. cyclohepatidenones
  21644. cycloheptane
  21645. cycloheptanes
  21646. cycloheptanoids
  21647. cycloheptene
  21648. cycloheptenone
  21649. cyclohexadiene
  21650. cyclohexadienes
  21651. cyclohexane
  21652. cyclohexanedione
  21653. cyclohexanes
  21654. cyclohexanones
  21655. cyclohexene
  21656. cyclohexene
  21657. synthesis
  21658. cyclohexenediols
  21659. cyclohexenone
  21660. cyclohexenones
  21661. cycloisomerization
  21662. cyclomaltoheptaose
  21663. cyclometalation
  21664. cyclooctadiene
  21665. cyclooctane
  21666. cyclooctatetraene
  21667. cyclooctatriene
  21668. cyclooctatriene
  21669. cyclooctenones
  21670. cycloolefins
  21671. cyclop
  21672. cyclopalladated
  21673. cyclopalladated
  21674. compounds
  21675. allyl
  21676. palladium
  21677. complexes
  21678. trans
  21679. cyclopenta
  21680. cyclopentadiene
  21681. cyclopentadiene
  21682. thermolysis
  21683. cyclopentadienes
  21684. cyclopentane
  21685. cyclopentanediones
  21686. cyclopentanediyl
  21687. cyclopentanes
  21688. cyclopentanoids
  21689. cyclopentanone
  21690. cyclopentanone
  21691. disubstituted
  21692. cuprate
  21693. addition
  21694. conjugate
  21695. cyclopentanones
  21696. cyclopentene
  21697. opentene
  21698. synthesis
  21699. cyclopentenol
  21700. cyclopentenone
  21701. cyclopentenone
  21702. synthesis
  21703. cyclopentenone
  21704. wittig
  21705. internal
  21706. cyclization
  21707. preparation
  21708. revie
  21709. cyclopentenones
  21710. cyclopentenyl
  21711. cyclopeptides
  21712. cyclophane
  21713. cyclophanes
  21714. cyclophilin
  21715. cyclopropanation
  21716. rearrangement
  21717. alpha
  21718. diazo
  21719. ketones
  21720. cyclopropanation
  21721. rearrangement
  21722. decomposition
  21723. cyclopropanations
  21724. cyclopropanations
  21725. ketones
  21726. cyclopropaneD
  21727. cyclopropane
  21728. amino
  21729. acids
  21730. cyclopropane
  21731. asymmetric
  21732. rhodium
  21733. diazo
  21734. transition
  21735. metal
  21736. carbe
  21737. cyclopropane
  21738. cyclopropylog
  21739. methanolog
  21740. constraints
  21741. enhanced
  21742. cyclopropane
  21743. opening
  21744. cyclopropane
  21745. review
  21746. synthesis
  21747. hudlicky
  21748. cyclopropane
  21749. cyclopropane
  21750. synthesis
  21751. oxygen
  21752. review
  21753. cyclopropanecarboxyl
  21754. cyclopropanes
  21755. cyclopropanol
  21756. cyclopropanone
  21757. cyclopropanones
  21758. cyclopropanylidene
  21759. cycloproparene
  21760. cycloproparenes
  21761. cycloproparenes
  21762. acene
  21763. biscycloproparene
  21764. polyacene
  21765. chemistry
  21766. cyclopropene
  21767. cyclopropene
  21768. carbene
  21769. vinyl
  21770. addition
  21771. review
  21772. synthesis
  21773. baird
  21774. cyclopropene
  21775. opening
  21776. vinyl
  21777. carbene
  21778. novel
  21779. insertion
  21780. cyclopropenes
  21781. cyclopropenes
  21782. dimethyl
  21783. substituted
  21784. cyclopropenylzinc
  21785. cyclopropenone
  21786. cyclopropenone
  21787. ketals
  21788. diels
  21789. alder
  21790. cyclopropene
  21791. target
  21792. tropol
  21793. cyclopropenone
  21794. ketals
  21795. diels
  21796. alder
  21797. cyclopropene
  21798. target
  21799. tropol
  21800. cyclopropenylstannan
  21801. cyclopropenylzinc
  21802. cyclopropyl
  21803. cyclopropyl
  21804. building
  21805. blocks
  21806. strained
  21807. compounds
  21808. cycloaddi
  21809. cyclopropyl
  21810. sulfide
  21811. ceric
  21812. radical
  21813. cation
  21814. opening
  21815. dicati
  21816. cyclopropylcarbinyl
  21817. cyclopropylcarbinyll
  21818. cyclopropylmethyl
  21819. cyclopropylog
  21820. cycloreversion
  21821. cycloreversions
  21822. cyclosporin
  21823. cyclotrimerization
  21824. cytochalasins
  21825. cytochrome
  21826. cytochrome
  21827. model
  21828. compounds
  21829. oxygenase
  21830. model
  21831. metall
  21832. cytovaricin
  21833. biotin
  21834. erythro
  21835. sphingosine
  21836. threo
  21837. sphingosine
  21838. organic
  21839. synthesis
  21840. fructose
  21841. gcattaatgc
  21842. assignments
  21843. ribonolactone
  21844. organic
  21845. synthesis
  21846. threo
  21847. sphingosine
  21848. stereoselective
  21849. synthesis
  21850. serine
  21851. d'angelo
  21852. d'angelo
  21853. review
  21854. alkylation
  21855. ketone
  21856. methodology
  21857. experimental
  21858. d-glucosamine
  21859. d-glucose
  21860. d-unsaturated
  21861. d2-isoxazoline
  21862. d2so4
  21863. dabco
  21864. daboun
  21865. daboun
  21866. heterocycle
  21867. nitrogen
  21868. synthesis
  21869. review
  21870. imine
  21871. ketone
  21872. dagonnean
  21873. dagonnean
  21874. hindered
  21875. amine
  21876. preparation
  21877. review
  21878. dakin-west
  21879. danheiser
  21880. danishefshy
  21881. danishefshy
  21882. biology
  21883. review
  21884. writing
  21885. mitomycin
  21886. aziridine
  21887. danishefsky
  21888. danishefsky
  21889. opening
  21890. nucleophile
  21891. synthesis
  21892. cyclopropane
  21893. danishefsky
  21894. sdiene
  21895. danishefsky's
  21896. danishefsky's
  21897. diene
  21898. danishevsky
  21899. darzen
  21900. darzens
  21901. daunomycin
  21902. david
  21903. davies
  21904. davis
  21905. orine
  21906. dazodiazaphosphorine
  21907. halides
  21908. oxidation
  21909. oxidation
  21910. aromatization
  21911. oxidation
  21912. indole
  21913. dealkoxycarbonylatio
  21914. dealkylation
  21915. deallylation
  21916. deamination
  21917. deamination
  21918. reactions
  21919. rearrangement
  21920. homocub
  21921. decompos
  21922. dearomatization
  21923. debruin
  21924. decalin
  21925. decarbomethoxylation
  21926. decarbonylation
  21927. decarboxylation
  21928. decarboxylation
  21929. decarboxylative
  21930. decomplexation
  21931. decomposition
  21932. decyanation
  21933. dipolar
  21934. cycloaddition
  21935. cyclopropene
  21936. review
  21937. strain
  21938. additi
  21939. defficient
  21940. deficient
  21941. dehydration
  21942. burgess
  21943. reagent
  21944. dehydroamino
  21945. dehydrobromination
  21946. dehydrogenase
  21947. dehydrogenation
  21948. dehydrogenation
  21949. dehydrohalogenation
  21950. dehydrotoluene
  21951. delocalization
  21952. delocalized
  21953. delta
  21954. deltacyclenes
  21955. deltate
  21956. delucchi
  21957. delucchi
  21958. alkyne
  21959. cycloaddition
  21960. diels
  21961. alder
  21962. synthesis
  21963. methodol
  21964. demand
  21965. demetalation
  21966. demethoxydaunomycino
  21967. demethylation
  21968. demethylsuberosin
  21969. demuth
  21970. demuth
  21971. review
  21972. triflate
  21973. silicon
  21974. alkylation
  21975. preparation
  21976. reagen
  21977. denmark
  21978. dennis
  21979. denovo
  21980. deoxycarbonylation
  21981. deoxyg
  21982. deoxygenation
  21983. genation
  21984. epoxide
  21985. deoxymannojirimycin
  21986. dependence
  21987. dependent
  21988. dependent
  21989. charge
  21990. delocalization
  21991. absorption
  21992. spectra
  21993. deprotect
  21994. deprotection
  21995. deprotection
  21996. method
  21997. reductive
  21998. cleavage
  21999. organic
  22000. reactions
  22001. deprotection
  22002. ester
  22003. alcohol
  22004. deprotection
  22005. silyl
  22006. ether
  22007. deprotection
  22008. tbdps
  22009. ether
  22010. deprotonation
  22011. depsipeptide
  22012. deriv
  22013. derivative
  22014. derivatives
  22015. derivatives
  22016. derivatives
  22017. fragmentation
  22018. cyclization
  22019. nitrogen
  22020. derivatives
  22021. reactivity
  22022. carbanions
  22023. derivatives
  22024. system
  22025. derivatives/dithioes
  22026. derived
  22027. deshong
  22028. deshong
  22029. h2sif6
  22030. design
  22031. designed
  22032. desilylation
  22033. desilylsulfonation
  22034. dess-martin
  22035. dess-martin
  22036. oxidation
  22037. dess-martin
  22038. periodinane
  22039. oxidation
  22040. desulfonylation
  22041. desulfonylation
  22042. sulfone
  22043. sulfonyl
  22044. carbanion
  22045. addition
  22046. desulfonylation
  22047. lithium
  22048. naphthalenide
  22049. alkylation
  22050. alpha
  22051. sulfo
  22052. desulfonylation
  22053. method
  22054. desulfurisation
  22055. desulfurization
  22056. etection
  22057. determination
  22058. determining
  22059. dethioacetalization
  22060. detosylation
  22061. deuterium
  22062. deutero
  22063. devices
  22064. di-grignard
  22065. di-iron
  22066. diacetate
  22067. diacetate
  22068. oxidation
  22069. diacetoxyiodo
  22070. benzene
  22071. cyclization
  22072. aranor
  22073. diacetoxyiodo
  22074. diacetyl
  22075. diacetylenes
  22076. diacid
  22077. diactivation
  22078. dialdehyde
  22079. dialdehydes
  22080. dialkoxy
  22081. dialkoxyboryl
  22082. dialkyl
  22083. dialkyl
  22084. dialkyl
  22085. reagent
  22086. dialkylamides
  22087. dialkylaminonitriles
  22088. dialkylcuprate
  22089. dialkylzinc
  22090. dialkylzinc
  22091. reagent
  22092. dialkylzincs
  22093. diallyl
  22094. diamine
  22095. diamine
  22096. system
  22097. diamine
  22098. ligand
  22099. diamine
  22100. synthesis
  22101. synthesis
  22102. diast
  22103. diaster
  22104. diastereo
  22105. diastereochem
  22106. diastereocontrol
  22107. diastereofacial
  22108. diastereofacial
  22109. selectivity
  22110. asymmetric
  22111. synthesis
  22112. design
  22113. diastereogenic
  22114. diastereomer
  22115. diastereoselection
  22116. diastereoselectiv
  22117. diastereoselectiveI
  22118. asymmetric
  22119. review
  22120. stereochem
  22121. diastereoselective
  22122. alkylation
  22123. diastereoselective
  22124. conjugate
  22125. addition
  22126. silyl
  22127. ether
  22128. rearrangem
  22129. diastereoselective
  22130. hydrogenation
  22131. diastereoselective
  22132. nucleophilic
  22133. addition
  22134. chiral
  22135. ketones
  22136. diastereoselective
  22137. o-alkylation
  22138. diastereoselective
  22139. radical
  22140. reaction
  22141. diastereoselectiviti
  22142. diastereoselectivity
  22143. diasteroselectivity
  22144. diatomic
  22145. diatomic
  22146. sulfur
  22147. generation
  22148. chemistry
  22149. sulfenyl
  22150. diaza
  22151. diazaanthracenes
  22152. diazabicyclo
  22153. diazabicycloundecene
  22154. diazabutadienes
  22155. diazadienes
  22156. diazaketones
  22157. diazaphenalenes
  22158. diazaphenanthrenes
  22159. diazaphenanthrenes
  22160. diazaanthracenes
  22161. diazaphenalenes
  22162. triazaph
  22163. diazapyraceheptylene
  22164. diazapyracyclenes
  22165. diazapyrenes
  22166. diazepines
  22167. diazepines
  22168. dioxepins
  22169. dithiepins
  22170. oxazepines
  22171. thiazepines
  22172. triaz
  22173. diazetidines
  22174. diazetidines
  22175. oxazetidines
  22176. thiazetidines
  22177. dioxetanes
  22178. oxathieta
  22179. diazide
  22180. diazine
  22181. diazine
  22182. metalation
  22183. diazirene
  22184. diaziridines
  22185. diaziridinimines
  22186. diaziridinones
  22187. diazirine
  22188. diazirines
  22189. diazo
  22190. diazo
  22191. aldehyde
  22192. reduction
  22193. lithiate
  22194. ester
  22195. carbanion
  22196. condensati
  22197. diazo
  22198. amide
  22199. ester
  22200. diazo
  22201. carbene
  22202. alkyne
  22203. rearrangement
  22204. propargylene
  22205. cyclopropana
  22206. diazo
  22207. carbene
  22208. substitution
  22209. cation
  22210. mechanism
  22211. electron
  22212. transfe
  22213. diazo
  22214. carbenoid
  22215. rhodium
  22216. insertion
  22217. solvent
  22218. diastereoselect
  22219. diazo
  22220. carbonyl
  22221. rhodium
  22222. carbenoid
  22223. cyclohexanedione
  22224. alkyne
  22225. diazo
  22226. carbonyl
  22227. rhodium
  22228. carbenoid
  22229. vinyl
  22230. ester
  22231. cyclopropanatio
  22232. diazo
  22233. compounds
  22234. metal
  22235. catalyzed
  22236. decomposition
  22237. carbonyl
  22238. ylide
  22239. diazo
  22240. ester
  22241. diazo
  22242. ketone
  22243. azide
  22244. transfer
  22245. review
  22246. experimental
  22247. writing
  22248. diazo
  22249. ketone
  22250. carbonyl
  22251. lewis
  22252. expansion
  22253. aluminum
  22254. diazo
  22255. ketone
  22256. coupling
  22257. diazo
  22258. ketone
  22259. cyclization
  22260. target
  22261. review
  22262. addition
  22263. aromatic
  22264. diazo
  22265. pyrrole
  22266. intramolecular
  22267. rhodium
  22268. stepwise
  22269. opening
  22270. diazo
  22271. wolff
  22272. ketene
  22273. laser
  22274. flash
  22275. photolysis
  22276. diazoacetate
  22277. diazoacetic
  22278. diazoacetophenone
  22279. diazoacetophenone
  22280. derivatives
  22281. diazoalkane
  22282. diazocarbonyl
  22283. diazocarbonyl
  22284. diazocines
  22285. diazoester
  22286. diazoester
  22287. coupling
  22288. aldehyde
  22289. diazoketoester
  22290. diazoketone
  22291. diazolactam
  22292. zoniu
  22293. diazonium
  22294. diazonium
  22295. diazotization
  22296. diazotization
  22297. dibal
  22298. dibal
  22299. reduction
  22300. dibenzodioxins
  22301. dibenzothiopyrans
  22302. dibenzyl
  22303. diborane
  22304. dibromide
  22305. dibromoethane
  22306. dibutyltin
  22307. dibutyltin
  22308. oxide
  22309. dicarbonic
  22310. dicarbonyl
  22311. dicarbonyl
  22312. coupling
  22313. titanium
  22314. reductive
  22315. mcmurry
  22316. ester
  22317. indole
  22318. dicarbonyls
  22319. dicarboximides
  22320. dicarboxylic
  22321. dicarboxylic
  22322. lactone
  22323. dication
  22324. dications
  22325. dichloro
  22326. dichloroallyllithium
  22327. dichloroborane
  22328. dichloroketene
  22329. dichloromethyl
  22330. dichloromethyl
  22331. dimethylchlorosilane
  22332. hydroxymethylidene
  22333. dirad
  22334. dicobalt
  22335. dicobalt
  22336. octacarbonyl
  22337. dicollidine
  22338. dictyopterene
  22339. dieckmann
  22340. annulation
  22341. diedrich
  22342. diels
  22343. diels
  22344. alder
  22345. diels
  22346. alder
  22347. approach
  22348. functionalized
  22349. hydroisoquinolines
  22350. diels
  22351. alder
  22352. cycloaddition
  22353. chiral
  22354. dichloroborane
  22355. catalyst
  22356. diels
  22357. alder
  22358. cycloaddition
  22359. intramolecular
  22360. diels
  22361. alder
  22362. cycloaddition
  22363. hydrophobic
  22364. effect
  22365. review
  22366. diels
  22367. alder
  22368. imine
  22369. review
  22370. cycloaddition
  22371. heterocyclic
  22372. schiff
  22373. diels
  22374. alder
  22375. nucleosides
  22376. derivatives
  22377. diels
  22378. alder
  22379. oligomerizations
  22380. substrate
  22381. directed
  22382. synthesis
  22383. diels
  22384. alder
  22385. pressure
  22386. volume
  22387. introduction
  22388. activation
  22389. transiti
  22390. diels
  22391. alder
  22392. reaction
  22393. amino
  22394. analysis
  22395. epoxy
  22396. resins
  22397. conven
  22398. diels
  22399. alder
  22400. reaction
  22401. chemical
  22402. reactivity
  22403. topological
  22404. aspects
  22405. diels
  22406. alder
  22407. reaction
  22408. electron
  22409. olefins
  22410. product
  22411. distribut
  22412. diels
  22413. alder
  22414. reaction
  22415. intramolecular
  22416. aldol
  22417. reaction
  22418. hydroazul
  22419. diels
  22420. alder
  22421. reaction
  22422. lewis
  22423. acids
  22424. diels
  22425. alder
  22426. reaction
  22427. organic
  22428. synthesis
  22429. lithium
  22430. enolate
  22431. diels
  22432. alder
  22433. reaction
  22434. pipecolic
  22435. derivatives
  22436. formal
  22437. total
  22438. diels
  22439. alder
  22440. reaction
  22441. platelet
  22442. activating
  22443. factor
  22444. derivatives
  22445. diels
  22446. alder
  22447. reaction
  22448. reagent
  22449. diels
  22450. alder
  22451. reactions
  22452. diels
  22453. alder
  22454. reactions
  22455. vinylindoles
  22456. rearrangements
  22457. vinylind
  22458. diels
  22459. alder
  22460. reactions
  22461. dihydro
  22462. dithiins
  22463. desulfonylation
  22464. diels
  22465. alder
  22466. reactions
  22467. participation
  22468. aldehydes
  22469. sulfonami
  22470. diels
  22471. alder
  22472. reactions
  22473. aklavinone
  22474. diels
  22475. alder
  22476. reactions
  22477. annellated
  22478. indole
  22479. access
  22480. vinylindoles
  22481. diels
  22482. alder
  22483. reactions
  22484. asymmetric
  22485. synthesis
  22486. additions
  22487. diels
  22488. alder
  22489. reactions
  22490. conjugated
  22491. carbodiimides
  22492. diels
  22493. alder
  22494. reactions
  22495. catalysis
  22496. diels
  22497. alder
  22498. reactions
  22499. catalyzed
  22500. reactions
  22501. dieno
  22502. pyranosides
  22503. diels
  22504. alder
  22505. reactions
  22506. chiral
  22507. lewis
  22508. acids
  22509. organic
  22510. synthesis
  22511. diels
  22512. alder
  22513. reactions
  22514. condensed
  22515. pyridazines
  22516. transformat
  22517. diels
  22518. alder
  22519. reactions
  22520. cycloaddition
  22521. reactions
  22522. sesquinorb
  22523. diels
  22524. alder
  22525. reactions
  22526. derivatives
  22527. hydrazones
  22528. pyridine
  22529. diels
  22530. alder
  22531. reactions
  22532. reaction
  22533. diastereofacial
  22534. selectivi
  22535. diels
  22536. alder
  22537. reaction
  22538. reagent@
  22539. diels
  22540. alder
  22541. reactions
  22542. ethers
  22543. denovo
  22544. synthesis
  22545. natural
  22546. diels-alder
  22547. diels-alder
  22548. cyclization@
  22549. diels-alder
  22550. cycloaddition@
  22551. diels-alder
  22552. reaction/diastereofa
  22553. reactivity/allylic
  22554. substitu@
  22555. dienenitriles@
  22556. diethylaminosulfur@
  22557. digonal
  22558. dihydroxylation
  22559. reaction@
  22560. diiodide
  22561. dimers@
  22562. dimethyldioxirane
  22563. oxidation
  22564. diolefin@
  22565. electron
  22566. diffraction
  22567. determination@
  22568. electrophilic
  22569. elimination
  22570. enantiogenic
  22571. enantioselective
  22572. enantioselective
  22573. total
  22574. synthesis@
  22575. enediyne
  22576. enolate
  22577. enones
  22578. epoxidation
  22579. epoxide
  22580. alkyne
  22581. acetylide
  22582. opening
  22583. review
  22584. carbanion
  22585. metal@
  22586. epoxide
  22587. review
  22588. opening
  22589. telluride
  22590. alkene
  22591. chiral
  22592. racemate@
  22593. equivalent
  22594. ester
  22595. esters
  22596. ether
  22597. ethylthioketene
  22598. expansion
  22599. nctional
  22600. groups
  22601. biotransformations
  22602. vitamin
  22603. diels
  22604. alder
  22605. reactions
  22606. ethers
  22607. denovo
  22608. synthesis
  22609. natural
  22610. diels
  22611. alder
  22612. reactions
  22613. fused
  22614. nitrogen
  22615. heterocycles
  22616. amino
  22617. diels
  22618. alder
  22619. reactions
  22620. pressure
  22621. organic
  22622. synthesis
  22623. diels
  22624. alder
  22625. reactions
  22626. isoxazolidinium
  22627. salts
  22628. cycloaddition
  22629. diels
  22630. alder
  22631. reactions
  22632. designed
  22633. bleomycins
  22634. metal
  22635. binding
  22636. diels
  22637. alder
  22638. reactions
  22639. nucleophilic
  22640. addition
  22641. acrylates
  22642. diels
  22643. alder
  22644. reactions
  22645. organic
  22646. synthesis
  22647. diels
  22648. alder
  22649. reactions
  22650. system
  22651. diels
  22652. alder
  22653. reactions
  22654. stereochemical
  22655. aspects
  22656. transition
  22657. diels
  22658. alder
  22659. reactions
  22660. tandem
  22661. inter
  22662. pyrrolidines
  22663. olefi
  22664. diels
  22665. alder
  22666. sulfone
  22667. deprotection
  22668. desulfonylation
  22669. review
  22670. diels-alder
  22671. diels-alder
  22672. cycloaddition
  22673. diels-alder
  22674. cycloaddition
  22675. reaction
  22676. diels-alder
  22677. reaction
  22678. ubstitu
  22679. diels-alder
  22680. reactions/promoted
  22681. organic-reactions/cy
  22682. conditio
  22683. diels-alder
  22684. reactions/resemble
  22685. grandfather
  22686. glucose/diacetone
  22687. diels/23-unsaturated
  22688. dienamine
  22689. diene
  22690. diene
  22691. alkene
  22692. zirconocene
  22693. zirconacyclopentane
  22694. transmetalation
  22695. diene
  22696. ester
  22697. diene
  22698. juglone
  22699. quinone
  22700. methyl
  22701. glyoxylate
  22702. cyclohexene
  22703. dihydrop
  22704. diene
  22705. synthesis
  22706. dienediyne
  22707. dienediynes
  22708. dienenitriles
  22709. dienes
  22710. dienes/carbohydrate
  22711. dieno
  22712. dienol
  22713. dienolate
  22714. dienols
  22715. dienones
  22716. dienophile
  22717. dienophiles
  22718. dienyl
  22719. dienyne
  22720. dienynes
  22721. diester
  22722. diesters
  22723. diethyl
  22724. diethyl
  22725. azodicarboxylate
  22726. esterification
  22727. reaction
  22728. triphenylph
  22729. diethyl
  22730. azodicarboxylate
  22731. triphenylphosphine
  22732. diethyl
  22733. diethylaluminium
  22734. diethylaluminum
  22735. diethylaluminum
  22736. chloride
  22737. diethylisopropylsily
  22738. ether
  22739. diethylzinc
  22740. diethylzinc
  22741. addition
  22742. diffraction
  22743. diffusing
  22744. difluoroalkyl
  22745. digonal
  22746. digonal
  22747. dihydro
  22748. dihydrodiazinediones
  22749. dihydrofuran
  22750. dihydrofuran
  22751. anion
  22752. lithiate
  22753. addition
  22754. vinyl
  22755. carbanion
  22756. lactone
  22757. dihydrofuran
  22758. synthesis
  22759. dihydrofuranone
  22760. dihydrofurans
  22761. dihydroindene
  22762. dihydroisoquinoline
  22763. dihydroisoquinoline
  22764. synthesis
  22765. dihydronicotinamide
  22766. dihydrooxazole
  22767. dihydrooxazole
  22768. ligand
  22769. dihydropyran
  22770. dihydropyran
  22771. opening
  22772. dihydropyran
  22773. synthesis
  22774. dihydropyrans
  22775. dihydropyrans
  22776. alpha
  22777. hydroxy
  22778. protection
  22779. dioxanone
  22780. dihydropyridin
  22781. dihydropyridine
  22782. dihydropyridines
  22783. dihydropyridones
  22784. dihydropyrimidinones
  22785. dihydropyrone
  22786. dihydropyrrol
  22787. dihydrosesamin
  22788. dihydrothiazine
  22789. dihydroxyaldehyde
  22790. dihydroxylation
  22791. iodide
  22792. diiodide
  22793. diiodo
  22794. diiodobicyclo
  22795. diiodosamarium
  22796. diisobutylaluminium
  22797. diisopinocampheylbor
  22798. diisopropylazodicarb
  22799. diketene
  22800. diketene
  22801. halides
  22802. derivatives
  22803. diketene
  22804. review
  22805. references
  22806. additive
  22807. aldrich
  22808. dicarbonyl
  22809. diketoester
  22810. diketone
  22811. diketones
  22812. dimer
  22813. dimeric
  22814. dimerization
  22815. dimethyl
  22816. dimethyl
  22817. acetal
  22818. dimethyl
  22819. acetylenedicarboxyla
  22820. homogeneous
  22821. catalysis
  22822. control
  22823. dimethyl
  22824. dimethylacetonide
  22825. dimethylamino
  22826. dimethylbenzofurans
  22827. dimethylbromoborane
  22828. dimethylchlorosilane
  22829. dimethylchromene
  22830. dimethylcuprate
  22831. dimethylcyclopropene
  22832. dimethyldioxirane
  22833. dimethyldioxirane
  22834. phenyl
  22835. phenylsulfonyloxazir
  22836. dimethyldioxirane
  22837. oxidation
  22838. dimethyldioxirane
  22839. oxidation
  22840. dimethyldioxirane
  22841. singlet
  22842. oxygen
  22843. dimethylindole
  22844. dimeth
  22845. dimethyldioxirene
  22846. dimethylhydrazones
  22847. dimethylidenes
  22848. dimethylindole
  22849. dimethylmalonate
  22850. dimethyloxosulfonium
  22851. dimethylphenylsilane
  22852. dimethylpyrrolidine
  22853. dimethylsilyl
  22854. dimethylsulfoxonium
  22855. dimethylzinc
  22856. dimroth
  22857. dinaphth
  22858. dinitroarenes
  22859. dinoreudesmanolides
  22860. dinuclear
  22861. diolD
  22862. protection
  22863. synthesis
  22864. dione
  22865. diones
  22866. dioxaazabicyclo
  22867. dioxaborolidine
  22868. dioxadiazetidines
  22869. dioxadiazines
  22870. dioxadithiepins
  22871. dioxanes
  22872. dioxanone
  22873. dioxasilaheterocycle
  22874. dioxathiazepines
  22875. dioxathiazines
  22876. dioxathietanes
  22877. dioxathiolanes
  22878. dioxathioles
  22879. dioxazetidines
  22880. dioxazines
  22881. dioxenes
  22882. dioxepins
  22883. dioxetane
  22884. dioxetanes
  22885. dioxide
  22886. dioxides
  22887. dioximes
  22888. dioxin
  22889. dioxinone
  22890. dioxins
  22891. dioxins
  22892. dithiins
  22893. dibenzodioxins
  22894. phenoxathiins
  22895. thianthrenes
  22896. dioxirane
  22897. dioxirane
  22898. epoxide
  22899. writing
  22900. review
  22901. oxidation
  22902. introduction
  22903. dioxirane
  22904. oxidation
  22905. reagent
  22906. epoxide
  22907. epoxidation
  22908. review
  22909. dioxiranes
  22910. dioxirene
  22911. dioxirene
  22912. reagent
  22913. oxidizing
  22914. review
  22915. dimethyldioxirene
  22916. amine
  22917. dioxo
  22918. dioxocanes
  22919. dioxocarboxylic
  22920. dioxocins
  22921. dioxolane
  22922. dioxolanes
  22923. dioxolanes
  22924. oxathiolanes
  22925. dioxygen
  22926. dipamp
  22927. dipamp
  22928. synthesis
  22929. dipeptide
  22930. diphenyl
  22931. diphenyl
  22932. disulfide
  22933. cyclization
  22934. diphenylamines
  22935. diphenylcarbene
  22936. diphenylditelluride
  22937. diphenylisopropoxyls
  22938. diphenylisopropoxyls
  22939. ether
  22940. diphenylmethyl
  22941. diphenylmethyl
  22942. ester
  22943. diphenylnitrilimine
  22944. diphenylnitrilimine
  22945. stereochemistry
  22946. regiochemistry
  22947. reactivit
  22948. diphenylzinc
  22949. dipivaloylmethanato
  22950. dipolar
  22951. dipolar
  22952. aprotic
  22953. media
  22954. ketoesters
  22955. dipolar
  22956. cycloaddition
  22957. dipolar
  22958. cycloaddition
  22959. nitrile
  22960. oxide
  22961. dipole
  22962. review
  22963. target
  22964. dipolar
  22965. cycloaddition
  22966. review
  22967. azomethine
  22968. ylide
  22969. pyridine
  22970. hydro
  22971. dipolar
  22972. cycloadditions
  22973. tetrahydrofurans
  22974. conversion
  22975. dipolar
  22976. cycloadditions
  22977. tetrahydrofurans
  22978. conversion
  22979. dipolarophiles
  22980. dipole
  22981. dipole
  22982. stabilized
  22983. anions
  22984. lithioamine
  22985. dipoles
  22986. dipyridyl
  22987. diradical
  22988. adical
  22989. mechanism
  22990. diradical
  22991. trimethylenemethane
  22992. intramolecular
  22993. hydrogen
  22994. abstra
  22995. diradicals
  22996. directed
  22997. directed
  22998. lithiation
  22999. directed
  23000. metalation
  23001. directed
  23002. metalation
  23003. group
  23004. directed
  23005. metallation
  23006. directing
  23007. directing
  23008. group
  23009. directionality
  23010. director
  23011. dirhodium
  23012. disease
  23013. diselenolan
  23014. diselenoles
  23015. disiamylborane
  23016. disilane
  23017. dispersal
  23018. dispersed
  23019. displacement
  23020. displacements
  23021. disproportionation
  23022. dissociation
  23023. dissolving
  23024. dissymmetric
  23025. distamycin
  23026. distannylethene
  23027. distribution
  23028. disub
  23029. disubstituted
  23030. disulfide
  23031. disulfides
  23032. disulfonamide
  23033. disulfonamide
  23034. dialkyl
  23035. system
  23036. functionaliz
  23037. disulphides
  23038. ditellurolanes
  23039. ditelluroles
  23040. dithiacyclooctane
  23041. dithiadiazepines
  23042. dithiadiazetidines
  23043. dithiadiazines
  23044. dithiane
  23045. dithiane
  23046. enantioselectivity
  23047. lithiate
  23048. carbanion
  23049. epoxide
  23050. dithianes
  23051. dithiazetidines
  23052. dithiazetidines
  23053. dithiazines
  23054. dithieno
  23055. dithiepins
  23056. dithietan
  23057. dithietanes
  23058. dithiins
  23059. dithioacetal
  23060. dithioacetals
  23061. dithiocanes
  23062. dithiocarbamates
  23063. dithiocarboxylic
  23064. dithioketal
  23065. olane
  23066. dithiolanes
  23067. dithiolanes
  23068. dithiolones
  23069. dithiolethiones
  23070. iminodithioles
  23071. dithi
  23072. dithiolethiones
  23073. dithiolones
  23074. dithiolyli
  23075. dithiolylium
  23076. dittmer
  23077. dittmer
  23078. chiral
  23079. asymmetric
  23080. epoxidation
  23081. tellurium
  23082. sharpless
  23083. dittmer
  23084. cyclobutene
  23085. sulfur
  23086. thiete
  23087. synthesis
  23088. heterocycle
  23089. diversity
  23090. divinyl
  23091. diradical
  23092. extrusion
  23093. nitrogen
  23094. trapping
  23095. review
  23096. regioselec
  23097. diyne
  23098. diyne
  23099. bergman
  23100. diradical
  23101. writing
  23102. rearrangement
  23103. triggering
  23104. diynes
  23105. dmtsf
  23106. cleavage
  23107. dodecahedranes
  23108. dodecane
  23109. doebner
  23110. doetz
  23111. doetz
  23112. carbene
  23113. fischer
  23114. complex
  23115. cycloaddition
  23116. review
  23117. alkyne
  23118. dolastatin
  23119. dolphin
  23120. dolphin
  23121. chemistry
  23122. organic
  23123. student
  23124. woodward
  23125. nobel
  23126. review
  23127. domino
  23128. donor
  23129. donor
  23130. acceptor
  23131. cyclopropane
  23132. opening
  23133. epoxide
  23134. electrophil
  23135. dopamine
  23136. dopants
  23137. double
  23138. double
  23139. double
  23140. interactions
  23141. exchange
  23142. double
  23143. hydroxylation
  23144. reaction
  23145. copper
  23146. reagents
  23147. double
  23148. isotope
  23149. fractionation
  23150. double
  23151. mediatory
  23152. system
  23153. indirect
  23154. electrooxidation
  23155. alcohols
  23156. double
  23157. michael
  23158. addition
  23159. annulation
  23160. dougherty
  23161. dowex
  23162. drawing
  23163. drewes
  23164. drimane
  23165. drummondii
  23166. dulcis
  23167. dunitzI
  23168. duphos
  23169. duphos
  23170. ligand
  23171. durst
  23172. durst
  23173. carbanion
  23174. sulfone
  23175. review
  23176. alkylation
  23177. duthaler
  23178. duthaler
  23179. amino
  23180. acids
  23181. review
  23182. sensitized
  23183. photooxygenation
  23184. photosensitized
  23185. oxygenation
  23186. dynamics
  23187. dynemicin
  23188. dynemicin
  23189. dynemicin
  23190. chemistry
  23191. analog
  23192. ketal
  23193. organic
  23194. synthesis
  23195. ethylidenecyclopropa
  23196. juaristi
  23197. cuevas
  23198. anomeric
  23199. effect
  23200. acetal
  23201. orthoester
  23202. review
  23203. early
  23204. eaton
  23205. echinoruber
  23206. eckstein
  23207. eckstein
  23208. oxazine
  23209. cyclization
  23210. methodology
  23211. synthesis
  23212. conformat
  23213. ediates
  23214. eduction
  23215. effect
  23216. effect
  23217. effective
  23218. effective
  23219. aldol
  23220. synthesis
  23221. hydroxy
  23222. esters
  23223. reformatsky
  23224. react
  23225. effects
  23226. efficient
  23227. efficient
  23228. addition
  23229. efficient
  23230. catalyst
  23231. efficient
  23232. lactones
  23233. valerolactones
  23234. route
  23235. gamma
  23236. efficient
  23237. synthesis
  23238. efficient
  23239. synthesis
  23240. pyran
  23241. derivatives
  23242. cardioactive
  23243. efficient
  23244. synthesis
  23245. acetylenes
  23246. alkynes
  23247. efficient
  23248. synthesis
  23249. cyanohydrins
  23250. alcohols
  23251. sulfoxides
  23252. acyloin
  23253. efficient
  23254. synthesis
  23255. lactones
  23256. eguchi
  23257. eguchi
  23258. carbonyl
  23259. review
  23260. writing
  23261. cycloaddition
  23262. introducti
  23263. eight
  23264. eight
  23265. membered
  23266. lactone
  23267. synthesis
  23268. elastase
  23269. elecrophilic
  23270. electrocatalytic
  23271. electrocatalytic
  23272. reduction
  23273. electroch
  23274. electrochem
  23275. electrochemical
  23276. electrochemical
  23277. electrochemical
  23278. oxidation
  23279. organosilicon
  23280. compounds
  23281. heteroatom
  23282. electrochemistry
  23283. electrochemistry
  23284. electrochemical
  23285. anodic
  23286. substitution
  23287. electrocyclc
  23288. electrocyclic
  23289. electrocyclic
  23290. reaction
  23291. ctrocyclization
  23292. electrolysis
  23293. electrolytic
  23294. electron
  23295. electron
  23296. correlation
  23297. energy
  23298. electron
  23299. defficient
  23300. electron
  23301. diffraction
  23302. determination
  23303. electron
  23304. paramagnetic
  23305. resonance
  23306. trans
  23307. carotene
  23308. cation
  23309. electron
  23310. arene
  23311. amination
  23312. azodicarboxylate
  23313. indole
  23314. electron
  23315. resonance
  23316. absolute
  23317. constants
  23318. butyl
  23319. electron
  23320. resonance
  23321. bridges
  23322. bonds
  23323. parallel
  23324. electron
  23325. transfer
  23326. transfer
  23327. electron
  23328. transfer
  23329. outer
  23330. sphere
  23331. inner
  23332. sphere
  23333. complexes
  23334. fragme
  23335. electron-deficient
  23336. electron-deficient
  23337. olefin
  23338. electron-transfer
  23339. electronegativities
  23340. electronic
  23341. electronic
  23342. control
  23343. hyperconjugation
  23344. carbon
  23345. electronic
  23346. structure
  23347. norbornadiene
  23348. interconversion
  23349. derivativ
  23350. electroorganic
  23351. electroorganic
  23352. chemistry
  23353. pyrrolidines
  23354. electrooxidation
  23355. electrophile
  23356. electrophiles
  23357. electrophiles
  23358. metals
  23359. electrophilic
  23360. electrophilic
  23361. electrophilic
  23362. amination
  23363. lithium
  23364. butyl
  23365. tosyloxycarbama
  23366. electrophilic
  23367. aromatic
  23368. substitution
  23369. electrophilic
  23370. fluorinations
  23371. polysubstituted
  23372. aromatics
  23373. cesium
  23374. electrophilic
  23375. closure
  23376. electrophilic
  23377. substitution
  23378. isocyanates
  23379. alpha
  23380. electroreduction
  23381. element
  23382. elemental
  23383. elguero
  23384. elguero
  23385. eliel
  23386. eliel
  23387. amine
  23388. chiral
  23389. naphthyl
  23390. resolution
  23391. optical
  23392. induction
  23393. eliel
  23394. chelation
  23395. addition
  23396. cram's
  23397. aldehyde
  23398. alcohol
  23399. carban
  23400. eliel
  23401. wilen
  23402. stereochemistry
  23403. symmetry
  23404. resolution
  23405. conformation
  23406. elimanation
  23407. elimination
  23408. elimination
  23409. elimination
  23410. diester
  23411. eliminations
  23412. eliminations
  23413. cyclization
  23414. ellaneous
  23415. ellipticine
  23416. elnagdi
  23417. elnagdi
  23418. diazo
  23419. dipolar
  23420. cycloaddition
  23421. higher
  23422. order
  23423. dipole
  23424. elnagdi
  23425. nitrile
  23426. heterocycle
  23427. synthesis
  23428. reagent
  23429. review
  23430. unsatur
  23431. elucidation
  23432. ement
  23433. emical
  23434. emission
  23435. emmons
  23436. enamide
  23437. enamide
  23438. diene
  23439. diels
  23440. alder
  23441. molybdenum
  23442. carbene
  23443. catalyzed
  23444. olefi
  23445. enamine
  23446. enamine
  23447. condenation
  23448. enamines
  23449. enaminones
  23450. enantiodivergent
  23451. enantiogeni
  23452. enantiogenic
  23453. enantiogenic
  23454. enantiogenic
  23455. reactions
  23456. asymmetric
  23457. homogeneous
  23458. catalysis
  23459. enantiomer
  23460. enantiomeric
  23461. enantiomerically
  23462. enantiomerically
  23463. dihydropyrimidinones
  23464. organotin
  23465. compoun
  23466. enantiomers
  23467. enantiopure
  23468. enantiopure
  23469. alkoxyallenes
  23470. propargyl
  23471. ethers
  23472. chiral
  23473. auxilia
  23474. enantioselective
  23475. enantioselective
  23476. enantioselective
  23477. addition
  23478. asymmetric
  23479. syntheses
  23480. reductions
  23481. enantioselective
  23482. addition
  23483. phytotoxic
  23484. enantioselective
  23485. aldol
  23486. reaction
  23487. enantioselective
  23488. alkylation
  23489. enantioselective
  23490. asymmetric
  23491. dihydroxylation
  23492. enantioselective
  23493. borane
  23494. ketone
  23495. reduction
  23496. enantioselective
  23497. formation
  23498. enantioselective
  23499. catalysis
  23500. allyl
  23501. palladium
  23502. complexes
  23503. enantioselective
  23504. diethyl
  23505. addition
  23506. enantioselective
  23507. hydrogenation
  23508. reaction
  23509. schiff
  23510. titanium
  23511. alkoxide
  23512. enantioselective
  23513. reduction
  23514. enantioselective
  23515. synthesis
  23516. enantioselective
  23517. synthesis
  23518. nitrocyclohexanones
  23519. enantioselective
  23520. synthesis
  23521. anodic
  23522. oxidation
  23523. lysine
  23524. enantioselective
  23525. synthesis
  23526. carbapenem
  23527. antibiotics
  23528. route
  23529. enantioselective
  23530. total
  23531. synthesis
  23532. enantioselective
  23533. total
  23534. synthesis
  23535. antibiotic
  23536. 61405
  23537. routien
  23538. enantioselectivity
  23539. enantioselectivity
  23540. asymmetric
  23541. aldol
  23542. reaction
  23543. enantiospecific
  23544. enantiselective
  23545. enatiogenic
  23546. endage
  23547. selective
  23548. cyclization
  23549. endor
  23550. reactions
  23551. reductive
  23552. elimination
  23553. reductive
  23554. elimination
  23555. enediyne
  23556. enediyne
  23557. antibiotics
  23558. enediyne
  23559. antiobiotic
  23560. enediyne
  23561. antiobiotics
  23562. enediynes
  23563. enedyne
  23564. enedyne
  23565. antibiotics
  23566. eneone
  23567. energetic
  23568. energies
  23569. energy
  23570. eneyne
  23571. eneynes
  23572. engel
  23573. engel
  23574. extrusion
  23575. mechanism
  23576. coupling
  23577. nitrogen
  23578. diradical
  23579. enhanced
  23580. enhancement
  23581. enkephalin
  23582. enlargement
  23583. enoate
  23584. enoates
  23585. carbenoids
  23586. ethyl
  23587. diazoacetate
  23588. ethers
  23589. ethers
  23590. ketones
  23591. cyclizations
  23592. acylsilanes
  23593. epoxides
  23594. reagen
  23595. ethers
  23596. vinylstannanes
  23597. silyl
  23598. ethers
  23599. benzeneselenenyl
  23600. triflate
  23601. trimethylsilyl
  23602. triflate
  23603. enolate
  23604. enolate
  23605. condensation
  23606. trimethylchlorosilan
  23607. enantio
  23608. enolates
  23609. enolization
  23610. enols
  23611. enone
  23612. enone
  23613. allyl
  23614. silane
  23615. cation
  23616. rearrangement
  23617. silyl
  23618. shift
  23619. enone
  23620. photochem
  23621. vinyl
  23622. carbene
  23623. cycloaddition
  23624. furan
  23625. cyclizatio
  23626. enone
  23627. photocycloaddition
  23628. intramolecular
  23629. allene
  23630. regiochem
  23631. enones
  23632. enones
  23633. enriched
  23634. enterobactin
  23635. entry
  23636. enyne
  23637. enynes
  23638. enzymatic
  23639. enzymatic
  23640. aldol
  23641. condensation
  23642. pseudomonas
  23643. mendocina
  23644. enzymatic
  23645. catalysis
  23646. enzyme
  23647. eonol
  23648. eparations
  23649. ephedrine
  23650. epibatidine
  23651. epibatidine
  23652. epibatidine
  23653. analogs
  23654. epimerization
  23655. episulfide
  23656. episulfide
  23657. elimination
  23658. alkene
  23659. boron
  23660. desulfurization
  23661. chiral
  23662. episulfone
  23663. episulfone
  23664. carbanion
  23665. silylation
  23666. ramberg
  23667. backlund
  23668. extrusion
  23669. episulfonium
  23670. episulphones
  23671. eposide
  23672. epoxidationG
  23673. epoxidation
  23674. dation
  23675. dihydroxylation
  23676. epoxidation
  23677. dioxirane
  23678. dimethyl
  23679. benzofurans
  23680. dimethyl
  23681. benzo
  23682. epoxidation
  23683. epoxide
  23684. catalyst
  23685. salen
  23686. manganese
  23687. enantioselec
  23688. epoxidations
  23689. epoxideE
  23690. epoxide
  23691. activation
  23692. epoxide
  23693. alkyne
  23694. acetylide
  23695. opening
  23696. review
  23697. carbanion
  23698. metal
  23699. epoxide
  23700. amine
  23701. aziridine
  23702. payne
  23703. rearrangement
  23704. sulfonamide
  23705. epoxide
  23706. asymmetric
  23707. synthesis
  23708. tellurium
  23709. epoxidation
  23710. sugar
  23711. epoxide
  23712. aziridine
  23713. deoxygenation
  23714. review
  23715. organo
  23716. transition
  23717. epoxide
  23718. carbanion
  23719. lithiate
  23720. stannane
  23721. addition
  23722. carbonyl
  23723. epoxide
  23724. cascade
  23725. grignard
  23726. nitrile
  23727. addition
  23728. epoxide
  23729. epoxidation
  23730. chiral
  23731. catalyst
  23732. review
  23733. asymmetric
  23734. induct
  23735. epoxide
  23736. epoxidation
  23737. manganese
  23738. salen
  23739. enantioselectivity
  23740. mecha
  23741. epoxide
  23742. migration
  23743. epoxide
  23744. opening
  23745. epoxide
  23746. openings
  23747. systems
  23748. epoxide
  23749. oxirane
  23750. payne
  23751. opening
  23752. cyclization
  23753. stereochem
  23754. epoxide
  23755. preparation
  23756. review
  23757. radical
  23758. closure
  23759. organometallic
  23760. epoxide
  23761. rearrangement
  23762. epoxide
  23763. review
  23764. chiral
  23765. epoxidation
  23766. catalyst
  23767. asymmetric
  23768. enanti
  23769. epoxide
  23770. review
  23771. metal
  23772. palladium
  23773. coupling
  23774. opening
  23775. cross
  23776. epoxide
  23777. review
  23778. opening
  23779. payne
  23780. alcohol
  23781. rearrangement
  23782. epoxide
  23783. review
  23784. opening
  23785. telluride
  23786. alkene
  23787. chiral
  23788. racemate
  23789. epoxide
  23790. opening
  23791. lfonium
  23792. ylide
  23793. allylic
  23794. alcohol
  23795. elimina
  23796. epoxide
  23797. opening
  23798. stannyl
  23799. cuprate
  23800. hydride
  23801. review
  23802. epoxide
  23803. synthesis
  23804. epoxide
  23805. titanium
  23806. opening
  23807. azide
  23808. review
  23809. lewis
  23810. organo
  23811. epoxide
  23812. vinylcyclopropane
  23813. conversion
  23814. allyl
  23815. anion
  23816. sulfide
  23817. epoxides
  23818. epoxy
  23819. epoxy
  23820. alcohols
  23821. epoxysilanes
  23822. aldehydes
  23823. epoxy
  23824. ester
  23825. epoxy
  23826. tosylate
  23827. epoxyalcohols
  23828. epoxyaldehydes
  23829. epoxyalkyl
  23830. epoxycyclohexanols
  23831. epoxysilanes
  23832. epoxysulfoxide
  23833. equatorial
  23834. equilibration
  23835. equilibrium
  23836. equivalent
  23837. equivalent
  23838. equivalents
  23839. equivalents
  23840. acetals
  23841. enones
  23842. ergot
  23843. ergot
  23844. alkaloid
  23845. erker
  23846. erker
  23847. imine
  23848. enamine
  23849. tautomeric
  23850. equilibrium
  23851. isonitrile
  23852. zircon
  23853. ermediates
  23854. erythro
  23855. erythro
  23856. sphinganine
  23857. triacetate
  23858. carbohydrate
  23859. reactions
  23860. mannos
  23861. erythromyci
  23862. erythromycin
  23863. erythronolide
  23864. erythronolide
  23865. escherichia
  23866. esker
  23867. esker
  23868. newcomb
  23869. radical
  23870. centered
  23871. aminyl
  23872. amidyl
  23873. pyrroli
  23874. esker
  23875. newcomb
  23876. radical
  23877. nitrogen
  23878. aminyl
  23879. cyclization
  23880. esker
  23881. newcomb
  23882. review
  23883. aminyl
  23884. radicals
  23885. pyrrolidine
  23886. esperamicin
  23887. esperamicins
  23888. spectroscopy
  23889. radical
  23890. clock
  23891. ester
  23892. ester
  23893. ester
  23894. enolate
  23895. aldol
  23896. condensation
  23897. ester
  23898. enolates
  23899. ester
  23900. hydroylsis
  23901. ester
  23902. chain
  23903. quassinoid
  23904. skeleton
  23905. enantioselective
  23906. synthe
  23907. esterase
  23908. esterification
  23909. esterification
  23910. macrolides
  23911. activation
  23912. lactones
  23913. esterification
  23914. officinalis
  23915. esterification
  23916. reaction
  23917. amines
  23918. esterification
  23919. reaction
  23920. diethyl
  23921. azodicarboxylate
  23922. esters
  23923. esters
  23924. estrogen
  23925. estrone
  23926. radicals
  23927. etallics
  23928. etallocenes
  23929. ethanethiol
  23930. ethanol
  23931. ethanol
  23932. intake
  23933. identification
  23934. ethenes
  23935. ethenone
  23936. ethenyl
  23937. ether
  23938. ether
  23939. ether
  23940. synthesis
  23941. ethers
  23942. methyl
  23943. ethoxy
  23944. ethoxymethylenemalon
  23945. ethyl
  23946. ethyl
  23947. acrylate
  23948. ethyl
  23949. alpha
  23950. hydroxymethyl
  23951. acrylate
  23952. rapid
  23953. synthesis
  23954. esters
  23955. ethylene
  23956. ethylenediazonium
  23957. ethylenediazonium
  23958. salts
  23959. ethylenic
  23960. ethylidenecyclopropa
  23961. ethylmagnesation
  23962. ethylthio
  23963. ethylthioketene
  23964. ethylthioketene
  23965. ethynylbenzene
  23966. etring
  23967. europium
  23968. europium
  23969. catalyzed
  23970. diels-alder
  23971. reaction
  23972. euryfuran
  23973. evaluation
  23974. evans
  23975. evans
  23976. chiral
  23977. auxiliary
  23978. evans
  23979. chiral
  23980. oxazolidinone
  23981. lithium
  23982. enolate
  23983. evans
  23984. copper
  23985. catalyst
  23986. aziridine
  23987. aziridination
  23988. chiral
  23989. asymmet
  23990. evans
  23991. aldol
  23992. reaction
  23993. evans
  23994. enolate
  23995. aldol
  23996. reaction
  23997. evans
  23998. tishchenko
  23999. evidence
  24000. excellence
  24001. exchange
  24002. methylene
  24003. exocyclic
  24004. exocyclic
  24005. lactones
  24006. hydroxy
  24007. methylene
  24008. butyrolactones
  24009. exocylic
  24010. expans
  24011. expansion
  24012. expansion
  24013. reactions
  24014. formation
  24015. expanxion
  24016. experimental
  24017. experimental
  24018. lithiate
  24019. review
  24020. carbanion
  24021. lithium
  24022. metal
  24023. tritrat
  24024. exploration
  24025. expressions
  24026. extension
  24027. extensive
  24028. extrusion
  24029. extrusion
  24030. nitrogen
  24031. carbonyl
  24032. ylide
  24033. cleavage
  24034. dialkoxy
  24035. carbene
  24036. nctional
  24037. groups
  24038. biotransformations
  24039. vitamin
  24040. nctional
  24041. groups
  24042. preparations
  24043. miscellaneous
  24044. nitriles
  24045. f3cso2x
  24046. f3cso3h
  24047. faces
  24048. facial
  24049. facile
  24050. facile
  24051. synthesis
  24052. regioselective
  24053. alkylation
  24054. stereoselective
  24055. factor
  24056. factors
  24057. failure
  24058. falck
  24059. falck
  24060. sulfone
  24061. alcohol
  24062. mitsunobu
  24063. cyclopentane
  24064. cyclobutane
  24065. falck
  24066. sulfone
  24067. bissulfone
  24068. reduction
  24069. writing
  24070. review
  24071. fallis
  24072. fallis
  24073. diels
  24074. alder
  24075. review
  24076. intramolecular
  24077. introduction
  24078. writin
  24079. fallis
  24080. radical
  24081. alpha
  24082. heteroatom
  24083. review
  24084. fallis
  24085. review
  24086. intramolecular
  24087. diels
  24088. alder
  24089. target
  24090. writing
  24091. family
  24092. farina
  24093. fatiadi
  24094. fatiadi
  24095. review
  24096. cyano
  24097. nitrile
  24098. preparation
  24099. synthesis
  24100. reagent
  24101. fatty
  24102. favorski
  24103. favorskii
  24104. favorsky
  24105. nctional
  24106. groups
  24107. biotransformations
  24108. vitamin
  24109. felkin
  24110. control@
  24111. first
  24112. fleming
  24113. synthesis
  24114. review
  24115. reagent
  24116. metal
  24117. silicon@
  24118. fluoroorganic
  24119. compounds
  24120. selective
  24121. fluorination
  24122. elemental
  24123. fluorosulfonate@
  24124. azirine
  24125. dipole
  24126. nitrile
  24127. ylide
  24128. cycloaddition@
  24129. freeman
  24130. writing
  24131. dihydro
  24132. isoxazole
  24133. heterocycle
  24134. rearrangement
  24135. functio@
  24136. functional
  24137. functional
  24138. groups
  24139. biotransformations
  24140. carbohydrates@
  24141. functional
  24142. groups
  24143. dissolving
  24144. metal
  24145. ketones
  24146. reduction
  24147. functional
  24148. groups
  24149. miscellaneous
  24150. reagents
  24151. selenium
  24152. dioxide
  24153. functional
  24154. groups
  24155. oxidation
  24156. ch-oh
  24157. functional
  24158. groups
  24159. oxidation
  24160. miscellaneous
  24161. reagents
  24162. functional
  24163. groups
  24164. preparations
  24165. alkenes
  24166. alkynes
  24167. acetylenes
  24168. functional
  24169. groups
  24170. preparations
  24171. alkenes
  24172. functional
  24173. groups
  24174. preparations
  24175. alkynes
  24176. functional
  24177. groups
  24178. preparations
  24179. ethers
  24180. acetals
  24181. c-o-c
  24182. ethe@
  24183. felkinI
  24184. felkin
  24185. adduct
  24186. felkin
  24187. addition
  24188. felkin
  24189. model
  24190. felkin-anh
  24191. addition
  24192. felkin-anh
  24193. felkin-anh
  24194. model
  24195. ferric
  24196. ferric
  24197. chloride
  24198. lewis
  24199. ferrocene
  24200. ferrocene
  24201. oxazoline
  24202. ferrocenylphosphine
  24203. ferroelectric
  24204. ferroelectric
  24205. liquid
  24206. crystals
  24207. enantioselective
  24208. synthesis
  24209. ferromagnets
  24210. fevig
  24211. ficini
  24212. ficini
  24213. review
  24214. ynamine
  24215. synthesis
  24216. intermediate
  24217. cycloaddition
  24218. field
  24219. fingerprints
  24220. tussock
  24221. pheromone
  24222. stereospecific
  24223. synthesis
  24224. first
  24225. first
  24226. fischer
  24227. fischer
  24228. carbene
  24229. complex
  24230. fischer
  24231. carbene
  24232. complex
  24233. writing
  24234. annulation
  24235. introduction
  24236. fischer
  24237. carbene
  24238. complexes
  24239. fischer
  24240. chromium
  24241. carbene
  24242. complex
  24243. review
  24244. writing
  24245. alkyne
  24246. pheno
  24247. fischer
  24248. chromium
  24249. carbene
  24250. writing
  24251. review
  24252. introduction
  24253. cycliza
  24254. fischer
  24255. review
  24256. nitro
  24257. ketone
  24258. carbanion
  24259. alkylation
  24260. preparation
  24261. fischer-hepp
  24262. fischer-tropsch
  24263. fisher
  24264. membered
  24265. carbocycle
  24266. synthesis
  24267. fk506
  24268. flash
  24269. flash
  24270. vacuum
  24271. pyrolysis
  24272. flash
  24273. vacuum
  24274. pyrolysis
  24275. spray
  24276. alkyne
  24277. cyclobutane
  24278. technique
  24279. flavan
  24280. flavanones
  24281. flavenes
  24282. flavone
  24283. flavones
  24284. fleming
  24285. fleming
  24286. review
  24287. silicon
  24288. silane
  24289. alkene
  24290. equivalent
  24291. reagent
  24292. fleming
  24293. synthesis
  24294. review
  24295. reagent
  24296. metal
  24297. silicon
  24298. florination
  24299. fluka
  24300. fluka
  24301. naked
  24302. fluoride
  24303. review
  24304. reagent
  24305. silicon
  24306. desilylation
  24307. fluka
  24308. sodium
  24309. acetylide
  24310. reagent
  24311. alkyne
  24312. acetylene
  24313. addition
  24314. fluorescens
  24315. fluorescent
  24316. fluoride
  24317. fluoride
  24318. naked
  24319. crown
  24320. ether
  24321. desilylation
  24322. review
  24323. fluorides
  24324. fluorinated
  24325. fluorination
  24326. fluorinations
  24327. fluorine
  24328. fluorine
  24329. chemistry
  24330. fluorine
  24331. spiroheterocycles
  24332. derivatives
  24333. fluoro
  24334. fluoro
  24335. organic
  24336. compounds
  24337. asymmetric
  24338. synthesis
  24339. difluoroalkyl
  24340. fluoroalkanesulfonat
  24341. fluoroborate
  24342. fluorocarbons
  24343. fluoromethyl
  24344. fluoroolefin
  24345. fluoroolefin
  24346. dipeptide
  24347. isosteres
  24348. stereoselective
  24349. synthesis
  24350. fluoroorganic
  24351. fluoroorganic
  24352. compounds
  24353. selective
  24354. fluorination
  24355. elemental
  24356. fluorosilane
  24357. fluorovinamidinium
  24358. fluoroxysulfate
  24359. fluviricin
  24360. fluviricin
  24361. aglycon
  24362. fodor
  24363. fodor
  24364. isoquinoline
  24365. nitrilium
  24366. mechanism
  24367. review
  24368. force
  24369. review
  24370. nitrenium
  24371. formal
  24372. formal
  24373. total
  24374. synthesis
  24375. asymmetric
  24376. total
  24377. synthesis
  24378. enantiosel
  24379. formaldehyde
  24380. formaldehyde
  24381. equivalent
  24382. formamide
  24383. formamidine
  24384. formamidines
  24385. format
  24386. formate
  24387. formati
  24388. formation
  24389. formation
  24390. formation
  24391. formation
  24392. formic
  24393. formylalkyl
  24394. formylation
  24395. forskolin
  24396. forster
  24397. found
  24398. fowler
  24399. fowler
  24400. review
  24401. azirine
  24402. dipole
  24403. nitrile
  24404. ylide
  24405. cycloaddition
  24406. photochem
  24407. review
  24408. carbanion
  24409. radical
  24410. electron
  24411. transfer
  24412. fr109615
  24413. fractionation
  24414. fragment
  24415. fragmentation
  24416. fragmentation
  24417. patterns
  24418. spectra
  24419. dihydro
  24420. phenyl
  24421. fragmentations
  24422. fragments
  24423. fragmetation
  24424. frame
  24425. framework
  24426. frameworks
  24427. franck
  24428. fredericamycin
  24429. radical
  24430. radical
  24431. addition
  24432. radical
  24433. additions
  24434. alkyl
  24435. radicals
  24436. stereoselectivity
  24437. radical
  24438. additions
  24439. butyl
  24440. peroxide
  24441. epoxy
  24442. propanat
  24443. radical
  24444. cyclization
  24445. radical
  24446. deoxygenation
  24447. radical
  24448. fragmetation
  24449. freeman
  24450. freeman
  24451. writing
  24452. dihydro
  24453. isoxazole
  24454. heterocycle
  24455. rearrangement
  24456. freitag
  24457. freitag
  24458. polycarbonate
  24459. review
  24460. structure
  24461. property
  24462. polymer
  24463. fremy's
  24464. frequencies
  24465. friedal
  24466. friedel
  24467. friedel
  24468. crafts
  24469. friedel
  24470. crafts
  24471. acylation
  24472. friedel
  24473. crafts
  24474. cyclialkylations
  24475. organic
  24476. synthesis
  24477. stereosele
  24478. friedel-crafts
  24479. friedel-crafts
  24480. acylation
  24481. friedlander
  24482. friedrichsen
  24483. friedrichsen
  24484. mesoionic
  24485. review
  24486. dipolar
  24487. cycloaddition
  24488. heterocy
  24489. fries
  24490. fries
  24491. rearrangement
  24492. fritscg-buttenberg-w
  24493. fructose
  24494. fruit
  24495. fuerstner
  24496. fukumoto
  24497. ional
  24498. groups
  24499. protection
  24500. hydroxyl
  24501. cf3so2x
  24502. silyl
  24503. funct
  24504. funct
  24505. groups
  24506. oxidation
  24507. alkenes
  24508. alkynes
  24509. ozone
  24510. funct
  24511. groups
  24512. preparations
  24513. alkenes
  24514. ketones
  24515. arylsulp
  24516. funct
  24517. groups
  24518. preparations
  24519. alkenes
  24520. m-c-c-x
  24521. functio
  24522. functio
  24523. groups
  24524. preparations
  24525. alkenes
  24526. physical
  24527. organic
  24528. functiona
  24529. functiona
  24530. groups
  24531. preparations
  24532. organosulphur
  24533. compounds
  24534. functiona
  24535. groups
  24536. transformations
  24537. functional
  24538. functional
  24539. functional
  24540. functional
  24541. preparations
  24542. ethers
  24543. hetring
  24544. epoxides
  24545. functional
  24546. transformations
  24547. electrochemical
  24548. reactions
  24549. functional
  24550. group
  24551. chemistry
  24552. functional
  24553. group
  24554. transformations
  24555. photochemical
  24556. reactions
  24557. functional
  24558. groups
  24559. biotransformations
  24560. functional
  24561. groups
  24562. biotransformations
  24563. carbohydrates
  24564. functional
  24565. groups
  24566. biotransformations
  24567. enzymes
  24568. functional
  24569. groups
  24570. biotransformations
  24571. enzymes
  24572. carbohydrates
  24573. functional
  24574. groups
  24575. biotransformations
  24576. hydrolysis
  24577. functional
  24578. groups
  24579. biotransformations
  24580. liver
  24581. ester
  24582. functional
  24583. groups
  24584. biotransformations
  24585. enantiog
  24586. functional
  24587. groups
  24588. biotransformations
  24589. reduction
  24590. catalytic
  24591. functional
  24592. groups
  24593. biotransformations
  24594. resolution
  24595. enantiogenic
  24596. functional
  24597. groups
  24598. cataly
  24599. hydrogenation
  24600. functional
  24601. groups
  24602. catalytic
  24603. genation
  24604. formation
  24605. functional
  24606. groups
  24607. catalytic
  24608. hydrogenation
  24609. alkenes
  24610. reduct
  24611. functional
  24612. groups
  24613. catalytic
  24614. hydrogenation
  24615. miscellaneous
  24616. functional
  24617. groups
  24618. catalytic
  24619. hydrogenation
  24620. enones
  24621. functional
  24622. groups
  24623. catalytic
  24624. hydrogenation
  24625. reduction
  24626. homogene
  24627. functional
  24628. groups
  24629. dissolving
  24630. metal
  24631. arenes
  24632. lithium
  24633. functional
  24634. groups
  24635. dissolving
  24636. metal
  24637. ketones
  24638. reduction
  24639. functional
  24640. groups
  24641. dissolving
  24642. metal
  24643. target
  24644. synthesis
  24645. miscella
  24646. functional
  24647. groups
  24648. eduction
  24649. metal
  24650. hydride
  24651. nabh4
  24652. borohydride
  24653. functional
  24654. groups
  24655. electrochemical
  24656. electrochemistry
  24657. functional
  24658. groups
  24659. electrochemical
  24660. mines
  24661. electrochemistry
  24662. functional
  24663. groups
  24664. enantiogenic
  24665. ketones
  24666. reduction
  24667. stere
  24668. functional
  24669. groups
  24670. metal
  24671. hydride
  24672. alkoxyaluminium
  24673. hydride
  24674. functional
  24675. groups
  24676. metal
  24677. hydride
  24678. alkoxyaluminium
  24679. hydrides
  24680. functional
  24681. groups
  24682. metal
  24683. hydride
  24684. boron
  24685. boranes
  24686. asymmetric
  24687. functional
  24688. groups
  24689. metal
  24690. hydride
  24691. r3snh
  24692. halides
  24693. reduc
  24694. functional
  24695. groups
  24696. metal
  24697. hydride
  24698. diborane
  24699. reduction
  24700. functional
  24701. groups
  24702. metal
  24703. hydride
  24704. physical
  24705. organic
  24706. rearrangeme
  24707. functional
  24708. groups
  24709. metal
  24710. hydride
  24711. reduction
  24712. selectivity
  24713. functional
  24714. groups
  24715. miscellaneous
  24716. c-c-x
  24717. c-c-x
  24718. haloke
  24719. functional
  24720. groups
  24721. miscellaneous
  24722. oxidation
  24723. isoquinoline
  24724. alkal
  24725. functional
  24726. groups
  24727. miscellaneous
  24728. reagents
  24729. selenium
  24730. dioxide
  24731. functional
  24732. groups
  24733. ch-oh
  24734. functional
  24735. groups
  24736. oxidati
  24737. alkenes
  24738. alkynes
  24739. singlet
  24740. functional
  24741. groups
  24742. oxidation
  24743. alkene
  24744. alkynes
  24745. dihydropyran
  24746. functional
  24747. groups
  24748. oxidation
  24749. alkenes
  24750. alkynes
  24751. functional
  24752. groups
  24753. oxidation
  24754. alkenes
  24755. alkynes
  24756. epoxidat
  24757. functional
  24758. groups
  24759. oxidation
  24760. alkenes
  24761. alkynes
  24762. diols
  24763. functional
  24764. groups
  24765. oxidation
  24766. alkenes
  24767. alkynes
  24768. epoxidation
  24769. functional
  24770. groups
  24771. oxidation
  24772. alkenes
  24773. alkynes
  24774. miscellaneou
  24775. functional
  24776. groups
  24777. oxidation
  24778. alkenes
  24779. alkynes
  24780. organometall
  24781. functional
  24782. groups
  24783. oxidation
  24784. alkenes
  24785. alkynes
  24786. alkanes
  24787. functional
  24788. groups
  24789. oxidation
  24790. alkenes
  24791. alkynes
  24792. permanganate
  24793. functional
  24794. groups
  24795. oxidation
  24796. alkenes
  24797. alkynes
  24798. photochemist
  24799. functional
  24800. groups
  24801. oxidation
  24802. alkenes
  24803. alkynes
  24804. functional
  24805. groups
  24806. oxidation
  24807. alkynes
  24808. alkenes
  24809. photooxidati
  24810. functional
  24811. groups
  24812. oxidation
  24813. ch-oh
  24814. functional
  24815. groups
  24816. oxidation
  24817. ch-oh
  24818. miscellaneou
  24819. reagen
  24820. functional
  24821. groups
  24822. oxidation
  24823. ch-oh
  24824. pyridinium
  24825. chloroch
  24826. functional
  24827. groups
  24828. oxidation
  24829. ch-oh
  24830. functional
  24831. groups
  24832. oxidation
  24833. electrochemical
  24834. functional
  24835. groups
  24836. oxidation
  24837. electrochemical
  24838. electrochemistry
  24839. functional
  24840. groups
  24841. oxidation
  24842. lkenes
  24843. alkynes
  24844. epoxidation
  24845. functional
  24846. groups
  24847. oxidation
  24848. miscellaneous
  24849. functional
  24850. groups
  24851. oxidation
  24852. miscellaneous
  24853. functional
  24854. groups
  24855. oxidation
  24856. miscellaneous
  24857. biotransformations
  24858. functional
  24859. groups
  24860. oxidation
  24861. miscellaneous
  24862. c-x-m
  24863. oxazi
  24864. functional
  24865. groups
  24866. oxidation
  24867. miscellaneous
  24868. tetraacetate
  24869. functional
  24870. groups
  24871. oxidation
  24872. miscellaneous
  24873. reactions
  24874. functional
  24875. groups
  24876. oxidation
  24877. miscellaneous
  24878. functional
  24879. groups
  24880. oxidation
  24881. miscellaneous
  24882. reagents
  24883. functional
  24884. groups
  24885. oxidation
  24886. miscellaneous
  24887. functional
  24888. groups
  24889. oxidation
  24890. miscellaneous
  24891. functional
  24892. groups
  24893. oxidation
  24894. miscellaneous
  24895. functional
  24896. groups
  24897. oxidation
  24898. miscellaneous
  24899. stereochemistry
  24900. functional
  24901. groups
  24902. eparations
  24903. heteroalkenes
  24904. enamine
  24905. functional
  24906. groups
  24907. eparations
  24908. organosulphur
  24909. compounds
  24910. functional
  24911. groups
  24912. preparatio
  24913. alkenes
  24914. miscellaneous
  24915. functional
  24916. groups
  24917. preparations
  24918. functional
  24919. groups
  24920. preparations
  24921. aldehydes
  24922. ketones
  24923. functional
  24924. groups
  24925. preparations
  24926. aldehydes
  24927. ketones
  24928. functional
  24929. groups
  24930. preparations
  24931. aldehydes
  24932. ketones
  24933. diketon
  24934. functional
  24935. groups
  24936. preparations
  24937. aldehydes
  24938. ketones
  24939. functional
  24940. groups
  24941. preparations
  24942. aldehydes
  24943. ketones
  24944. trans
  24945. functional
  24946. groups
  24947. preparations
  24948. alkenes
  24949. functional
  24950. groups
  24951. preparations
  24952. alkenes
  24953. 134-thiadizolines
  24954. functional
  24955. groups
  24956. preparations
  24957. alkenes
  24958. alkynes
  24959. acetylenes
  24960. functional
  24961. groups
  24962. preparations
  24963. alkenes
  24964. alkynes
  24965. functional
  24966. groups
  24967. preparations
  24968. alkenes
  24969. allenes
  24970. functional
  24971. groups
  24972. preparations
  24973. alkenes
  24974. allenes
  24975. stereochemist
  24976. functional
  24977. groups
  24978. preparations
  24979. alkenes
  24980. functional
  24981. groups
  24982. preparations
  24983. alkenes
  24984. amination
  24985. amines
  24986. functional
  24987. groups
  24988. preparations
  24989. alkenes
  24990. functional
  24991. groups
  24992. preparations
  24993. alkenes
  24994. inversion
  24995. isomeri
  24996. functional
  24997. groups
  24998. preparations
  24999. alkenes
  25000. isomerisation
  25001. functional
  25002. groups
  25003. preparations
  25004. alkenes
  25005. functional
  25006. groups
  25007. preparations
  25008. alkenes
  25009. sulfones
  25010. functional
  25011. groups
  25012. preparations
  25013. alkenes
  25014. chelotropic
  25015. episu
  25016. functional
  25017. groups
  25018. preparations
  25019. alkenes
  25020. diols
  25021. deoxygenatio
  25022. functional
  25023. groups
  25024. preparations
  25025. alkenes
  25026. heteroalkenes
  25027. esters
  25028. functional
  25029. groups
  25030. preparations
  25031. alkenes
  25032. aldehydes
  25033. functional
  25034. groups
  25035. preparations
  25036. alkenes
  25037. functional
  25038. groups
  25039. preparations
  25040. alkenes
  25041. aldeh
  25042. functional
  25043. groups
  25044. preparations
  25045. alkenes
  25046. organometallics
  25047. eleme
  25048. functional
  25049. groups
  25050. preparations
  25051. alkenes
  25052. organometallics
  25053. phosp
  25054. functional
  25055. groups
  25056. preparations
  25057. alkenes
  25058. organometallics
  25059. titan
  25060. functional
  25061. groups
  25062. preparations
  25063. alkenes
  25064. wittig
  25065. functional
  25066. groups
  25067. preparations
  25068. alkenes
  25069. phosphorus
  25070. stereochem
  25071. functional
  25072. groups
  25073. preparations
  25074. alkenes
  25075. stereochemistry
  25076. functional
  25077. groups
  25078. preparations
  25079. alkenes
  25080. synthons
  25081. cycloadditio
  25082. functional
  25083. groups
  25084. preparations
  25085. alkenes
  25086. wadsworth-emmons
  25087. functional
  25088. groups
  25089. preparations
  25090. alkenes
  25091. wittig
  25092. reaction
  25093. functional
  25094. groups
  25095. preparations
  25096. alkenes
  25097. wittig
  25098. reaction
  25099. functional
  25100. groups
  25101. preparations
  25102. alkynes
  25103. functional
  25104. groups
  25105. preparations
  25106. alkynes
  25107. alkynes
  25108. acetylenes
  25109. functional
  25110. groups
  25111. preparations
  25112. alkynes
  25113. acetylenes
  25114. 14-add
  25115. functional
  25116. groups
  25117. preparations
  25118. alkynes
  25119. functional
  25120. groups
  25121. preparations
  25122. alkynes
  25123. alkynylamines
  25124. functional
  25125. groups
  25126. preparations
  25127. alkynes
  25128. cc-c-m
  25129. functional
  25130. groups
  25131. preparations
  25132. alkynes
  25133. pericyclic
  25134. reactions
  25135. functional
  25136. groups
  25137. preparations
  25138. alkynes
  25139. ynamine
  25140. functional
  25141. groups
  25142. preparations
  25143. allenes
  25144. functional
  25145. groups
  25146. preparations
  25147. amidines
  25148. imidates
  25149. functional
  25150. groups
  25151. preparations
  25152. amines
  25153. gabriel
  25154. synthesis
  25155. functional
  25156. groups
  25157. preparations
  25158. amino
  25159. nitroso
  25160. nitro
  25161. functional
  25162. groups
  25163. preparations
  25164. azides
  25165. functional
  25166. groups
  25167. preparations
  25168. c-x-r
  25169. ethers
  25170. elimina
  25171. functional
  25172. groups
  25173. preparations
  25174. nh-so2
  25175. shapiro
  25176. functional
  25177. groups
  25178. preparations
  25179. aldehydes
  25180. functional
  25181. groups
  25182. preparations
  25183. florination
  25184. functional
  25185. groups
  25186. preparations
  25187. ethers
  25188. acetals
  25189. 13-dioxole
  25190. functional
  25191. groups
  25192. preparations
  25193. ethers
  25194. acetals
  25195. c-o-c
  25196. functional
  25197. groups
  25198. preparations
  25199. ethers
  25200. acetals
  25201. functional
  25202. groups
  25203. preparations
  25204. ethers
  25205. acetals
  25206. reduction
  25207. functional
  25208. groups
  25209. preparations
  25210. ethers
  25211. acetals
  25212. spiroaceta
  25213. functional
  25214. groups
  25215. preparations
  25216. ethers
  25217. acetals
  25218. transforma
  25219. functional
  25220. groups
  25221. preparations
  25222. ethers
  25223. acetalsroh
  25224. alcohol
  25225. functional
  25226. groups
  25227. preparations
  25228. ethers
  25229. functional
  25230. groups
  25231. preparations
  25232. heteroalkenes
  25233. acetylenes
  25234. functional
  25235. groups
  25236. preparations
  25237. heteroalkenes
  25238. vinyl
  25239. functional
  25240. groups
  25241. preparations
  25242. heteroalkenes
  25243. functional
  25244. groups
  25245. preparations
  25246. heteroalkenes
  25247. functional
  25248. groups
  25249. preparations
  25250. heteroalkenes
  25251. heterocycles
  25252. functional
  25253. groups
  25254. preparations
  25255. heteroalkenes
  25256. hetring
  25257. functional
  25258. groups
  25259. preparations
  25260. heteroalkenes
  25261. nitroalkenes
  25262. functional
  25263. groups
  25264. preparations
  25265. heteroalkenes
  25266. nitroenamines
  25267. functional
  25268. groups
  25269. preparations
  25270. heteroalkenes
  25271. nitroenamines
  25272. functional
  25273. groups
  25274. preparations
  25275. heteroalkenes
  25276. enami
  25277. functional
  25278. groups
  25279. preparations
  25280. heterocumulenes
  25281. functional
  25282. groups
  25283. preparations
  25284. heterocumulenes
  25285. functional
  25286. groups
  25287. preparations
  25288. heterocumulenes
  25289. functional
  25290. groups
  25291. preparations
  25292. heterocumulenes
  25293. azides
  25294. functional
  25295. groups
  25296. preparations
  25297. heterocumulenes
  25298. functional
  25299. groups
  25300. preparations
  25301. heterocumulenes
  25302. functional
  25303. groups
  25304. preparations
  25305. heterocumulenes
  25306. carbodiimides
  25307. functional
  25308. groups
  25309. preparations
  25310. heterocumulenes
  25311. diazonium
  25312. functional
  25313. groups
  25314. preparations
  25315. heterocumulenes
  25316. nso2cl
  25317. functional
  25318. groups
  25319. preparations
  25320. heterocumulenes
  25321. thioketen
  25322. functional
  25323. groups
  25324. preparations
  25325. heterocumulenes
  25326. functional
  25327. groups
  25328. preparations
  25329. heterocumulenes
  25330. functional
  25331. groups
  25332. preparations
  25333. heterocumulenes
  25334. functional
  25335. groups
  25336. preparations
  25337. heteroalkenes
  25338. nitroenamines
  25339. functional
  25340. groups
  25341. preparations
  25342. heterocumulenes
  25343. functional
  25344. groups
  25345. preparations
  25346. miscellaneous
  25347. acyloxylati@
  25348. functional
  25349. groups
  25350. preparations
  25351. miscellaneous
  25352. decarboxylation@
  25353. functional
  25354. groups
  25355. preparations
  25356. miscellaneous
  25357. methylene
  25358. lacto@
  25359. functional
  25360. groups
  25361. preparations
  25362. miscellaneous
  25363. synthons
  25364. functional
  25365. groups
  25366. preparations
  25367. organosulphur
  25368. compounds
  25369. c-x-y@
  25370. functional
  25371. groups
  25372. protection
  25373. amino
  25374. protection@
  25375. functional
  25376. groups
  25377. reduction
  25378. catalytic
  25379. hydrogenation
  25380. enantiog@
  25381. functional
  25382. groups
  25383. reduction
  25384. metal
  25385. hydride
  25386. hydrides
  25387. lialh4
  25388. functional
  25389. groups
  25390. transfo
  25391. mations
  25392. functional
  25393. groups
  25394. transformations
  25395. carbohydrates
  25396. functional
  25397. groups
  25398. transformations
  25399. cyclopropane
  25400. cleavage
  25401. phys@
  25402. functional
  25403. groups
  25404. transformations
  25405. oxidation
  25406. furan
  25407. furopyrimidines@
  25408. fusco@
  25409. general
  25410. functional
  25411. groups
  25412. preparations
  25413. heterocumulenes
  25414. functional
  25415. groups
  25416. preparations
  25417. heterocumulenes
  25418. functional
  25419. groups
  25420. preparations
  25421. tetraacetate
  25422. functional
  25423. groups
  25424. preparations
  25425. miscellane
  25426. darzens
  25427. perkin
  25428. functional
  25429. groups
  25430. preparations
  25431. miscellaneo
  25432. functional
  25433. groups
  25434. preparations
  25435. miscellaneous
  25436. functional
  25437. groups
  25438. preparations
  25439. miscellaneous
  25440. aldehydes
  25441. functional
  25442. groups
  25443. preparations
  25444. miscellaneous
  25445. amides
  25446. functional
  25447. groups
  25448. preparations
  25449. miscellaneous
  25450. amines
  25451. c-c-x
  25452. functional
  25453. groups
  25454. preparations
  25455. miscellaneous
  25456. amino
  25457. acids
  25458. functional
  25459. groups
  25460. preparations
  25461. miscellaneous
  25462. amino
  25463. acids
  25464. functional
  25465. groups
  25466. preparations
  25467. miscellaneous
  25468. azacrown
  25469. functional
  25470. groups
  25471. preparations
  25472. miscellaneous
  25473. functional
  25474. groups
  25475. preparations
  25476. miscellaneous
  25477. functional
  25478. groups
  25479. preparations
  25480. miscellaneous
  25481. acyloxylati
  25482. functional
  25483. groups
  25484. preparations
  25485. miscellaneous
  25486. functional
  25487. groups
  25488. preparations
  25489. miscellaneous
  25490. fluorides
  25491. functional
  25492. groups
  25493. preparations
  25494. miscellaneous
  25495. halides
  25496. functional
  25497. groups
  25498. preparations
  25499. miscellaneous
  25500. functional
  25501. groups
  25502. preparations
  25503. miscellaneous
  25504. functional
  25505. groups
  25506. preparations
  25507. miscellaneous
  25508. azides
  25509. functional
  25510. groups
  25511. preparations
  25512. miscellaneous
  25513. nitroso
  25514. functional
  25515. groups
  25516. preparations
  25517. miscellaneous
  25518. nitro
  25519. functional
  25520. groups
  25521. preparations
  25522. miscellaneous
  25523. functional
  25524. groups
  25525. preparations
  25526. miscellaneous
  25527. functional
  25528. groups
  25529. preparations
  25530. miscellaneous
  25531. functional
  25532. groups
  25533. preparations
  25534. miscellaneous
  25535. carboxylic
  25536. functional
  25537. groups
  25538. preparations
  25539. miscellaneous
  25540. cf3so3me
  25541. methyl
  25542. functional
  25543. groups
  25544. preparations
  25545. miscellaneous
  25546. cyanic
  25547. esters
  25548. functional
  25549. groups
  25550. preparations
  25551. miscellaneous
  25552. decarboxylation
  25553. functional
  25554. groups
  25555. preparations
  25556. miscellaneous
  25557. diols
  25558. functional
  25559. groups
  25560. preparations
  25561. miscellaneous
  25562. enantiogeni
  25563. functional
  25564. groups
  25565. preparations
  25566. miscellaneous
  25567. functional
  25568. groups
  25569. preparations
  25570. miscellaneous
  25571. fluorides
  25572. functional
  25573. groups
  25574. preparations
  25575. miscellaneous
  25576. fluorination
  25577. functional
  25578. groups
  25579. preparations
  25580. miscellaneous
  25581. glutaconaldehyd
  25582. functional
  25583. groups
  25584. preparations
  25585. miscellaneous
  25586. halogenation
  25587. functional
  25588. groups
  25589. preparations
  25590. miscellaneous
  25591. hetring
  25592. functional
  25593. groups
  25594. preparations
  25595. miscellaneous
  25596. c-c-x
  25597. functional
  25598. groups
  25599. preparations
  25600. miscellaneous
  25601. hooc-c-co
  25602. functional
  25603. groups
  25604. preparations
  25605. miscellaneous
  25606. imines
  25607. functional
  25608. groups
  25609. preparations
  25610. miscellaneous
  25611. isatonic
  25612. anhydr
  25613. functional
  25614. groups
  25615. preparations
  25616. miscellaneous
  25617. isoureas
  25618. esteri
  25619. functional
  25620. groups
  25621. preparations
  25622. miscellaneous
  25623. lactones
  25624. functional
  25625. groups
  25626. preparations
  25627. miscellaneous
  25628. methylene
  25629. lacto
  25630. functional
  25631. groups
  25632. preparations
  25633. miscellaneous
  25634. c-c-c-x
  25635. functional
  25636. groups
  25637. preparations
  25638. miscellaneous
  25639. c-c-x
  25640. fluor
  25641. functional
  25642. groups
  25643. preparations
  25644. miscellaneous
  25645. c-c-x
  25646. functional
  25647. groups
  25648. preparations
  25649. miscellaneous
  25650. nh-oh
  25651. functional
  25652. groups
  25653. preparations
  25654. miscellaneous
  25655. organofluorine
  25656. functional
  25657. groups
  25658. preparations
  25659. miscellaneous
  25660. orthocarbonic
  25661. functional
  25662. groups
  25663. preparations
  25664. miscellaneous
  25665. functional
  25666. groups
  25667. preparations
  25668. miscellaneous
  25669. peroxyamines
  25670. functional
  25671. groups
  25672. preparations
  25673. miscellaneous
  25674. pyridinium
  25675. functional
  25676. groups
  25677. preparations
  25678. miscellaneous
  25679. quinonoid
  25680. compo
  25681. functional
  25682. groups
  25683. preparations
  25684. miscellaneous
  25685. r3po3
  25686. functional
  25687. groups
  25688. preparations
  25689. miscellaneous
  25690. functional
  25691. groups
  25692. preparations
  25693. miscellaneous
  25694. functional
  25695. groups
  25696. preparations
  25697. miscellaneous
  25698. sulphur
  25699. functional
  25700. groups
  25701. preparations
  25702. miscellaneous
  25703. synthons
  25704. functional
  25705. groups
  25706. preparations
  25707. miscellaneous
  25708. tetrachlorometh
  25709. functional
  25710. groups
  25711. preparations
  25712. miscellaneous
  25713. thiohydroxamic
  25714. functional
  25715. groups
  25716. preparations
  25717. miscellaneous
  25718. transformations
  25719. functional
  25720. groups
  25721. preparations
  25722. miscellaneous
  25723. ureidoalkylatio
  25724. functional
  25725. groups
  25726. preparations
  25727. heterocycles
  25728. functional
  25729. groups
  25730. preparations
  25731. aldehydes
  25732. c-pr3
  25733. functional
  25734. groups
  25735. preparations
  25736. aldehydes
  25737. functional
  25738. groups
  25739. preparations
  25740. alkehydes
  25741. functional
  25742. groups
  25743. preparations
  25744. organometallics
  25745. boron
  25746. boronat
  25747. functional
  25748. groups
  25749. preparations
  25750. organosulphur
  25751. compounds
  25752. functional
  25753. groups
  25754. preparations
  25755. organosulphur
  25756. compounds
  25757. functional
  25758. groups
  25759. preparations
  25760. organosulphur
  25761. compounds
  25762. functional
  25763. groups
  25764. preparations
  25765. organosulphur
  25766. compounds
  25767. functional
  25768. groups
  25769. preparations
  25770. organosulphur
  25771. compounds
  25772. c-x-y
  25773. functional
  25774. groups
  25775. preparations
  25776. organosulphur
  25777. compounds
  25778. heter
  25779. functional
  25780. groups
  25781. preparations
  25782. organosulphur
  25783. compounds
  25784. functional
  25785. groups
  25786. preparations
  25787. organosulphur
  25788. compounds
  25789. functional
  25790. groups
  25791. preparations
  25792. organosulphur
  25793. compounds
  25794. functional
  25795. groups
  25796. preparations
  25797. organosulphur
  25798. compounds
  25799. sulfi
  25800. functional
  25801. groups
  25802. preparations
  25803. organosulphur
  25804. compounds
  25805. sulfu
  25806. functional
  25807. groups
  25808. preparations
  25809. organosulphur
  25810. compounds
  25811. sulph
  25812. functional
  25813. groups
  25814. preparations
  25815. organosulphur
  25816. compounds
  25817. sulto
  25818. functional
  25819. groups
  25820. preparations
  25821. organosulphur
  25822. compounds
  25823. thiir
  25824. functional
  25825. groups
  25826. preparations
  25827. peroxides
  25828. functional
  25829. groups
  25830. preparations
  25831. stereochemistry
  25832. hetring
  25833. functional
  25834. groups
  25835. preparations
  25836. transformations
  25837. functional
  25838. groups
  25839. preparations
  25840. transformations
  25841. nitrones
  25842. functional
  25843. groups
  25844. protection
  25845. amine
  25846. protection
  25847. functional
  25848. groups
  25849. protection
  25850. amino
  25851. protection
  25852. functional
  25853. groups
  25854. protection
  25855. carbonyl
  25856. carboxyl
  25857. hydroxyl
  25858. functional
  25859. groups
  25860. protection
  25861. carboxyl
  25862. acids
  25863. esterif
  25864. functional
  25865. groups
  25866. protection
  25867. hydroxyl
  25868. functional
  25869. groups
  25870. protection
  25871. hydroxyl
  25872. thers
  25873. cleavag
  25874. functional
  25875. groups
  25876. protection
  25877. miscellaneous
  25878. protection
  25879. functional
  25880. groups
  25881. ransformations
  25882. deltate
  25883. squarate
  25884. rhodizonat
  25885. functional
  25886. groups
  25887. reduc
  25888. dissolving
  25889. metal
  25890. organometallics
  25891. functional
  25892. groups
  25893. reduction
  25894. functional
  25895. groups
  25896. reduction
  25897. hydrometallation
  25898. functional
  25899. groups
  25900. reduction
  25901. hydrometallation
  25902. functional
  25903. groups
  25904. reduction
  25905. catalytic
  25906. hydrogena
  25907. functional
  25908. groups
  25909. reduction
  25910. catalytic
  25911. hydrogenation
  25912. functional
  25913. groups
  25914. reduction
  25915. catalytic
  25916. hydrogenation
  25917. arenes
  25918. functional
  25919. groups
  25920. reduction
  25921. catalytic
  25922. hydrogenation
  25923. functional
  25924. groups
  25925. reduction
  25926. catalytic
  25927. hydrogenation
  25928. enantiog
  25929. functional
  25930. groups
  25931. reduction
  25932. catalytic
  25933. hydrogenation
  25934. enantios
  25935. functional
  25936. groups
  25937. reduction
  25938. catalytic
  25939. hydrogenation
  25940. reductio
  25941. functional
  25942. groups
  25943. reduction
  25944. dissolving
  25945. metal
  25946. functional
  25947. groups
  25948. reduction
  25949. dissolving
  25950. metal
  25951. arenes
  25952. functional
  25953. groups
  25954. reduction
  25955. dissolving
  25956. metal
  25957. ketones
  25958. functional
  25959. groups
  25960. reduction
  25961. dissolving
  25962. metal
  25963. physical
  25964. organi
  25965. functional
  25966. groups
  25967. reduction
  25968. dissolving
  25969. metal
  25970. functional
  25971. groups
  25972. reduction
  25973. dissolving
  25974. metal
  25975. functional
  25976. groups
  25977. reduction
  25978. electrochemical
  25979. electrochemistry
  25980. functional
  25981. groups
  25982. reduction
  25983. metal
  25984. hydride
  25985. functional
  25986. groups
  25987. reduction
  25988. metal
  25989. hydride
  25990. alkoxyaluminohydri
  25991. functional
  25992. groups
  25993. reduction
  25994. metal
  25995. hydride
  25996. formation
  25997. functional
  25998. groups
  25999. reduction
  26000. metal
  26001. hydride
  26002. alkohols
  26003. functional
  26004. groups
  26005. reduction
  26006. metal
  26007. hydride
  26008. enantioselective
  26009. functional
  26010. groups
  26011. reduction
  26012. metal
  26013. hydride
  26014. hydrides
  26015. lialh4
  26016. functional
  26017. groups
  26018. reduction
  26019. metal
  26020. hydride
  26021. hydrides
  26022. reduction
  26023. functional
  26024. groups
  26025. reduction
  26026. metal
  26027. hydride
  26028. preparations
  26029. alken
  26030. functional
  26031. groups
  26032. reduction
  26033. metal
  26034. hydride
  26035. sodium
  26036. hydride
  26037. functional
  26038. groups
  26039. reduction
  26040. metal
  26041. hydrides
  26042. functional
  26043. groups
  26044. reduction
  26045. miscellaneous
  26046. aromatics
  26047. chain
  26048. functional
  26049. groups
  26050. reduction
  26051. miscellaneous
  26052. diimine
  26053. alkene
  26054. functional
  26055. groups
  26056. reduction
  26057. miscellaneous
  26058. functional
  26059. groups
  26060. reduction
  26061. miscellaneous
  26062. enantioselective
  26063. functional
  26064. groups
  26065. reduction
  26066. functional
  26067. groups
  26068. reduction
  26069. functional
  26070. groups
  26071. reduction
  26072. hydrometallation
  26073. functional
  26074. groups
  26075. reduction
  26076. hydrometallation
  26077. functional
  26078. groups
  26079. reparations
  26080. miscellaneous
  26081. functional
  26082. groups
  26083. ansformations
  26084. carbohydrates
  26085. useful
  26086. fragm
  26087. functional
  26088. groups
  26089. trans
  26090. ormations
  26091. functional
  26092. groups
  26093. transfo
  26094. mations
  26095. functional
  26096. groups
  26097. transformat
  26098. formation
  26099. appenda
  26100. functional
  26101. groups
  26102. transformat
  26103. functional
  26104. groups
  26105. transformatio
  26106. functional
  26107. groups
  26108. transformation
  26109. cyclopropane
  26110. cleavage
  26111. functional
  26112. groups
  26113. transformations
  26114. functional
  26115. groups
  26116. transformations
  26117. acetals
  26118. orthoest
  26119. functional
  26120. groups
  26121. transformations
  26122. functional
  26123. groups
  26124. transformations
  26125. x-c-c-y
  26126. hydrometall
  26127. functional
  26128. groups
  26129. transformations
  26130. functional
  26131. groups
  26132. transformations
  26133. c-nh2
  26134. amines
  26135. functional
  26136. groups
  26137. transformations
  26138. substituti
  26139. functional
  26140. groups
  26141. transformations
  26142. amines
  26143. functional
  26144. groups
  26145. transformations
  26146. functional
  26147. groups
  26148. transformations
  26149. triflic
  26150. functional
  26151. groups
  26152. transformations
  26153. carbohydrates
  26154. functional
  26155. groups
  26156. transformations
  26157. carbohydrates
  26158. functional
  26159. groups
  26160. transformations
  26161. carbohydrates
  26162. acetalisatio
  26163. functional
  26164. groups
  26165. transformations
  26166. carbohydrates
  26167. chirons
  26168. functional
  26169. groups
  26170. transformations
  26171. carbohydrates
  26172. oxidation
  26173. functional
  26174. groups
  26175. transformations
  26176. carbohydrates
  26177. physical
  26178. functional
  26179. groups
  26180. transformations
  26181. carbohydrates
  26182. protection
  26183. functional
  26184. groups
  26185. transformations
  26186. carbohydrates
  26187. target
  26188. synth
  26189. functional
  26190. groups
  26191. transformations
  26192. carbohydrates
  26193. useful
  26194. fragm
  26195. functional
  26196. groups
  26197. transformations
  26198. lopropane
  26199. cleavage
  26200. functional
  26201. groups
  26202. transformations
  26203. cyclop
  26204. opane
  26205. cleavage
  26206. functional
  26207. groups
  26208. transformations
  26209. cyclopropane
  26210. cleava
  26211. functional
  26212. groups
  26213. transformations
  26214. cyclopropane
  26215. cleavage
  26216. functional
  26217. groups
  26218. transformations
  26219. cyclopropane
  26220. cleavage
  26221. functional
  26222. groups
  26223. transformations
  26224. cyclopropane
  26225. cleavage
  26226. functional
  26227. groups
  26228. transformations
  26229. cyclopropane
  26230. cleavage
  26231. functional
  26232. groups
  26233. transformations
  26234. deoxygenation
  26235. esterificati
  26236. functional
  26237. groups
  26238. transformations
  26239. electroch
  26240. mical
  26241. reactions
  26242. functional
  26243. groups
  26244. transformations
  26245. electrochemical
  26246. reactions
  26247. functional
  26248. groups
  26249. transformations
  26250. epoxide
  26251. cleavage
  26252. functional
  26253. groups
  26254. transformations
  26255. epoxide
  26256. cleavage
  26257. etring
  26258. functional
  26259. groups
  26260. transformations
  26261. epoxide
  26262. cleavage
  26263. hetring
  26264. functional
  26265. groups
  26266. transformations
  26267. functional
  26268. groups
  26269. transformations
  26270. amides
  26271. functional
  26272. groups
  26273. transformations
  26274. dicarbonyls
  26275. functional
  26276. groups
  26277. transformations
  26278. diethyl
  26279. functional
  26280. groups
  26281. transformations
  26282. functional
  26283. groups
  26284. transformations
  26285. functional
  26286. groups
  26287. transformations
  26288. functional
  26289. groups
  26290. transformations
  26291. oxidation
  26292. functional
  26293. groups
  26294. transformations
  26295. photo
  26296. hemical
  26297. reactions
  26298. functional
  26299. groups
  26300. transformations
  26301. photochemical
  26302. reactions
  26303. functional
  26304. groups
  26305. transformations
  26306. preparations
  26307. miscellane
  26308. functionalisation
  26309. functionalization
  26310. functionalized
  26311. functionalized
  26312. arylcarbenes
  26313. phenylcarbene
  26314. rearrangement
  26315. functionalized
  26316. hydroisoquinolines
  26317. manzamine
  26318. tricyclic
  26319. functionalized
  26320. cyclic
  26321. ethers
  26322. hydroxy
  26323. carbonyls
  26324. relative
  26325. functionalized
  26326. macrocycles
  26327. molecular
  26328. inclusion
  26329. clathrate
  26330. functionalized
  26331. secondary
  26332. alcohols
  26333. aldehydes
  26334. reagents
  26335. chlorid
  26336. functions
  26337. furan
  26338. furan
  26339. annulation
  26340. allene
  26341. sulfonium
  26342. review
  26343. writing
  26344. diketone
  26345. furan
  26346. carbenoid
  26347. rhodium
  26348. diazo
  26349. carbonyl
  26350. addition
  26351. opening
  26352. furan
  26353. derivatives
  26354. thieno
  26355. pyridine
  26356. furan
  26357. electrophile
  26358. induced
  26359. cyclization
  26360. tetrahydrofuran
  26361. alken
  26362. furan
  26363. intramolecular
  26364. diels
  26365. alder
  26366. oxabicyclic
  26367. opening
  26368. furan
  26369. silyl
  26370. silicon
  26371. desilylation
  26372. fluoride
  26373. furan
  26374. synthesis
  26375. furanes
  26376. furanone
  26377. furanone
  26378. anion
  26379. carbanion
  26380. displacement
  26381. halide
  26382. intramolecular
  26383. furanones
  26384. furanophanes
  26385. furans
  26386. furazans
  26387. furoeremophilanes
  26388. furofurans
  26389. furopyrans
  26390. furopyrazines
  26391. furopyrazoles
  26392. furopyridazines
  26393. furopyridines
  26394. furopyridines
  26395. furopyridazines
  26396. furopyrimidines
  26397. furopyrazines
  26398. furopyrimidines
  26399. furopyrroles
  26400. furoquinolinedione
  26401. furoquinolines
  26402. furoquinoxalines
  26403. furoxans
  26404. furoxans
  26405. furazans
  26406. furstner
  26407. furylborate
  26408. hydrazine
  26409. hydrazidoyl
  26410. chloride
  26411. sigmatropic
  26412. rearrangeme
  26413. fused
  26414. fusion
  26415. alkylidene
  26416. lactone
  26417. lactones
  26418. g-amino
  26419. g-amino
  26420. acetylene
  26421. g-lactone
  26422. g-lactone
  26423. synthesis
  26424. g-trimethylsilyl
  26425. g-trimethylsilyl
  26426. allyl
  26427. boronates
  26428. g-trimethylsilyl
  26429. allyl
  26430. boronic
  26431. ester
  26432. g-trimethylsilyloxy
  26433. g-trimethylsilyloxy
  26434. nitrile
  26435. gabriel
  26436. galli
  26437. gamma
  26438. gamma
  26439. butyrolactones
  26440. claisen
  26441. rearrangement
  26442. lactonization
  26443. gamma
  26444. hydroxy
  26445. vinylstannanes
  26446. photooxygenation
  26447. singlet
  26448. oxygen
  26449. gamma-alkylation
  26450. gamma-cyanoketo
  26451. gamma-ketoesters
  26452. ganem
  26453. ganem
  26454. amidines
  26455. swainsonine
  26456. potent
  26457. deoxymannoj
  26458. ganometallics
  26459. garner
  26460. garner
  26461. aziridine
  26462. chiral
  26463. auxiliary
  26464. thermal
  26465. openin
  26466. phase
  26467. review
  26468. amine
  26469. alcohol
  26470. alkene
  26471. preparation
  26472. conversion
  26473. gassman
  26474. gassman
  26475. review
  26476. carbonium
  26477. electron
  26478. transfer
  26479. deficient
  26480. gausian
  26481. gaussian
  26482. gaussian
  26483. basis
  26484. functions
  26485. atomic
  26486. basis
  26487. first
  26488. atoms
  26489. gawley
  26490. gawley
  26491. oxazoline
  26492. chiral
  26493. lithium
  26494. lithiate
  26495. review
  26496. alkylation
  26497. gcattaatgc
  26498. dimethyl
  26499. group
  26500. stituents
  26501. genation
  26502. general
  26503. general
  26504. general
  26505. synthetic
  26506. equivalent
  26507. addition
  26508. reactions
  26509. cycloadditio
  26510. generation
  26511. generation
  26512. genes
  26513. geometrical
  26514. geometry
  26515. germabenzene
  26516. germacyclobuta
  26517. germacyclohexanes
  26518. germacyclopentanes
  26519. germacyclopentenes
  26520. germanium
  26521. germoles
  26522. gharbia
  26523. ghosez
  26524. ghosez
  26525. diene
  26526. diels
  26527. alder
  26528. intramolecular
  26529. review
  26530. azirine
  26531. giguere
  26532. gilchrist
  26533. gilchrist
  26534. nitroso
  26535. alkene
  26536. alkyne
  26537. review
  26538. diels
  26539. alder
  26540. gilday
  26541. ginsburg
  26542. ginsburg
  26543. review
  26544. dipolar
  26545. cycloaddition
  26546. orbital
  26547. symmetry
  26548. regio
  26549. giuliano
  26550. giuliano
  26551. franck
  26552. lopez
  26553. horton
  26554. leblanc
  26555. deshong
  26556. lubineau
  26557. gives
  26558. global
  26559. glucopyranose
  26560. glucose
  26561. se/asymmetric
  26562. glucose/asymmetric
  26563. glucose/diacetone
  26564. glucosidase
  26565. glutaconaldehyde
  26566. glutamic
  26567. glutamic
  26568. glycal
  26569. glycal
  26570. epoxide
  26571. glycals
  26572. glycals/aminoglycosi
  26573. glyceraldehyde
  26574. glycerol
  26575. glycidic
  26576. glycidic
  26577. ester
  26578. glycine
  26579. glycine
  26580. cation
  26581. equivalents
  26582. pipecolic
  26583. derivatives
  26584. acetal
  26585. glycine
  26586. enolate
  26587. imine
  26588. aldol
  26589. hydroxy
  26590. amino
  26591. asymmetr
  26592. glycoconjugate
  26593. glycolipids
  26594. glycols
  26595. glycopeptides
  26596. glycoprocessing
  26597. glycoprotein
  26598. glycoprotein
  26599. biosynthesis
  26600. inhibitors
  26601. acylnitroso
  26602. cycloadditi
  26603. glycosidasae
  26604. glycosidase
  26605. glycosidase
  26606. amidrazone
  26607. glycosidase
  26608. inhibitors
  26609. stereoselective
  26610. synthesis
  26611. organocoppe
  26612. glycosidases
  26613. glycoside
  26614. coupling
  26615. glycoside
  26616. formation
  26617. glucose/asymmetric@
  26618. glycoside
  26619. coupling@
  26620. glycoside
  26621. formation
  26622. glycosylation@
  26623. alcohols
  26624. cyano
  26625. groups
  26626. halides
  26627. hannessian@
  26628. heart@
  26629. hemiaminal
  26630. heteroannulations
  26631. heterocycle
  26632. heterodinuclear@
  26633. higher
  26634. order
  26635. cyano
  26636. cuprate@
  26637. hixson
  26638. cyclopropane
  26639. photorearrangement
  26640. diradical
  26641. review@
  26642. homoallylic
  26643. horner
  26644. emmons
  26645. olefination@
  26646. huisgen
  26647. thiocarbonyl
  26648. ylide
  26649. review
  26650. dipolar
  26651. cycloaddition
  26652. sulf@
  26653. hydride
  26654. hydrodesulfurization
  26655. hydrolysis
  26656. hydroxy
  26657. carbonyl
  26658. compounds@
  26659. hydroxypyridines@
  26660. iddon
  26661. thiophene
  26662. cycloaddition
  26663. opening
  26664. photochem
  26665. carbene@
  26666. imidazothiazines@
  26667. iminium
  26668. indene
  26669. indoles
  26670. carbazoles
  26671. isoindoles
  26672. indolizines@
  26673. induction
  26674. insertion
  26675. isocyanide
  26676. zirconium
  26677. complex@
  26678. intermediates
  26679. intramolecular
  26680. intramolecular
  26681. diels-alder@
  26682. glycoside
  26683. formation
  26684. glycosides
  26685. glycosides
  26686. alcohols
  26687. glycosphingolipids
  26688. glycosyl
  26689. glycosyl
  26690. fluorides
  26691. glycosylated
  26692. glycosylated
  26693. amino
  26694. acids
  26695. esters
  26696. tetrahydropyridines
  26697. glyoxylate
  26698. rearrangement
  26699. glyoxylic
  26700. goldman
  26701. goldman
  26702. review
  26703. synthesis
  26704. enantioselective
  26705. dihydro
  26706. pyridine
  26707. goldschmidt
  26708. gramine
  26709. grandfather
  26710. grateloupia
  26711. gribble
  26712. gribble
  26713. alkaloid
  26714. benzyne
  26715. diels
  26716. alder
  26717. cancer
  26718. review
  26719. oxidation
  26720. grieco
  26721. grieco
  26722. diazo
  26723. ketone
  26724. catalyst
  26725. intramolecular
  26726. cycloaddition
  26727. griganrd
  26728. grigard
  26729. grigard
  26730. reagent
  26731. grigg
  26732. grigg
  26733. azomethine
  26734. ylide
  26735. dipolar
  26736. cycloaddition
  26737. imine
  26738. tautomer
  26739. grignard
  26740. grignard
  26741. grignard
  26742. reagent
  26743. conjugated
  26744. diene
  26745. grignard
  26746. reagent
  26747. initiation
  26748. experimental
  26749. review
  26750. references
  26751. grignard
  26752. reagents
  26753. grignard
  26754. reagents
  26755. carbonyl
  26756. compounds
  26757. organolithium
  26758. grimmett
  26759. grimmett
  26760. imidazole
  26761. preparation
  26762. review
  26763. spectroscopy
  26764. heterocyc
  26765. groove
  26766. ground
  26767. ground
  26768. states
  26769. molecules
  26770. photoelectron
  26771. spectra
  26772. rearrangements
  26773. group
  26774. group
  26775. migration
  26776. deoxygenation
  26777. alcohols
  26778. cyano
  26779. group
  26780. migration
  26781. deoxygenation
  26782. alcohols
  26783. cyano
  26784. groups
  26785. groups
  26786. groups
  26787. grubbs
  26788. gschwend
  26789. gschwend
  26790. lithium
  26791. carbanion
  26792. heterocycle
  26793. review
  26794. alkylation
  26795. guanidine
  26796. guanines
  26797. guanosine
  26798. guanosine
  26799. analogs
  26800. guanosines
  26801. guest
  26802. gulonolactone
  26803. gunther
  26804. gunther
  26805. spectroscopy
  26806. review
  26807. inept
  26808. writing
  26809. gylcoside
  26810. gylcoside
  26811. synthesis
  26812. gymnodinium
  26813. gymnomitrol
  26814. bonds
  26815. brown
  26816. method
  26817. insertion
  26818. insertion
  26819. cyclopropanation
  26820. reactions
  26821. walborsky
  26822. topolski
  26823. carbanion
  26824. grignard
  26825. reagent
  26826. organoma
  26827. waldmann
  26828. lithium
  26829. perchlorate
  26830. solvolysis
  26831. substitution
  26832. revie
  26833. h-c-c-c-coor
  26834. h2sif6
  26835. dienyl
  26836. hadjipavloulitina
  26837. hadjipavloulitina
  26838. haemanthidine
  26839. hafnium
  26840. hageman
  26841. hageman
  26842. flash
  26843. thermal
  26844. experimental
  26845. technique
  26846. review
  26847. hajos
  26848. hajos
  26849. aldol
  26850. condensation
  26851. methodology
  26852. review
  26853. aldehyde
  26854. experim
  26855. halenaquinone
  26856. halichondria
  26857. halide
  26858. halides
  26859. halides
  26860. haller
  26861. haller
  26862. bauer
  26863. amide
  26864. carboxylic
  26865. saponification
  26866. cleavage
  26867. chloro
  26868. alpha
  26869. carbonyl
  26870. ketone
  26871. chemistry
  26872. review
  26873. kimpe
  26874. diazirene
  26875. extrusion
  26876. nitrogen
  26877. review
  26878. opening
  26879. carben
  26880. epoxide
  26881. olefin
  26882. haloallylboronate
  26883. haloamidation
  26884. haloarenes
  26885. haloboranes
  26886. haloboronic
  26887. halocarbanions
  26888. halocyclization
  26889. halocyclopropane
  26890. haloetherification
  26891. halogen
  26892. eaction
  26893. halogenated
  26894. halogenation
  26895. halogenoketones
  26896. halogenonitroalkanes
  26897. halogenosilanes
  26898. halogentaion
  26899. haloketones
  26900. halolactones
  26901. halolactonization
  26902. halosulfonium
  26903. hammett
  26904. hanack
  26905. hanack
  26906. review
  26907. carbanion
  26908. organometallic
  26909. anion
  26910. alken
  26911. hanisms
  26912. hannessian
  26913. hantzsch
  26914. hanzawaF
  26915. hanzawa
  26916. synlett
  26917. zirconium
  26918. zircocene
  26919. allyl
  26920. addition
  26921. alkene
  26922. haplophyllum
  26923. haplophyllum
  26924. tuberculatum
  26925. asymmetric
  26926. epoxidation
  26927. polyether
  26928. happens
  26929. harming
  26930. harpoon
  26931. hartwig
  26932. hartwig
  26933. review
  26934. deoxygenation
  26935. alcohol
  26936. alkane
  26937. radical
  26938. harwood
  26939. harwood
  26940. intramolecular
  26941. review
  26942. theory
  26943. calculations
  26944. diels
  26945. review
  26946. formyl
  26947. synthon
  26948. carbanion
  26949. umpolung
  26950. alkylatio
  26951. umpolung
  26952. methodology
  26953. review
  26954. synthesis
  26955. carbanion
  26956. alkylat
  26957. umpolung
  26958. review
  26959. equivalent
  26960. carbanion
  26961. alkylation
  26962. methodo
  26963. haslam
  26964. haslam
  26965. parameter
  26966. conversion
  26967. ester
  26968. methodology
  26969. review
  26970. hassner
  26971. hassner
  26972. azirine
  26973. nitrile
  26974. ylide
  26975. dipolar
  26976. cycloaddition
  26977. synthesi
  26978. hatanaka
  26979. triphenylphosphine
  26980. adduct
  26981. heaney
  26982. heaney
  26983. triflate
  26984. review
  26985. trimethylsilyl
  26986. silicon
  26987. catalyst
  26988. fluor
  26989. heart
  26990. heathcock
  26991. heats
  26992. addition
  26993. review
  26994. coupling
  26995. cyclization
  26996. palladium
  26997. indole
  26998. synthesis
  26999. enamide
  27000. mitomycin
  27001. skeleton
  27002. reaction
  27003. hegarty
  27004. hegarty
  27005. nitrile
  27006. dipole
  27007. imine
  27008. dipolar
  27009. nitrilium
  27010. alkylation
  27011. hegedus
  27012. hegedus
  27013. alkene
  27014. metal
  27015. catalyst
  27016. palladium
  27017. organometallic
  27018. subst
  27019. hegedus
  27020. palladium
  27021. cyclization
  27022. amine
  27023. alkene
  27024. heterocycle
  27025. revie
  27026. hegedus
  27027. review
  27028. organometallic
  27029. metal
  27030. transition
  27031. synthesis
  27032. hegedus
  27033. review
  27034. palladium
  27035. cyclization
  27036. indole
  27037. ortho
  27038. organometa
  27039. helicenes
  27040. hemetsberger
  27041. hemetsberger
  27042. isotope
  27043. effect
  27044. deuterium
  27045. photorearrangement
  27046. hemiacetal
  27047. hemiaminal
  27048. hemiaminal
  27049. hemical
  27050. hemistry
  27051. hemisynthesis
  27052. hemisynthesis
  27053. analogs
  27054. efficient
  27055. agents
  27056. henderson
  27057. henes
  27058. henry
  27059. henry
  27060. reaction
  27061. heptaazaphenalenes
  27062. heptane
  27063. heptanes
  27064. heptenoyl
  27065. herein
  27066. heritiera
  27067. heritiera
  27068. littoralis
  27069. mangrove
  27070. plants
  27071. cyclization
  27072. hetaryne
  27073. hetarynes
  27074. heter
  27075. hetero
  27076. hetero
  27077. diels
  27078. alder
  27079. reactions
  27080. chemoselectivity
  27081. regioselectivi
  27082. hetero-cope
  27083. hetero-diels-alder
  27084. hetero-diels-alder
  27085. reaction
  27086. heteroalkenes
  27087. heteroalkylation
  27088. heteroannulat
  27089. heteroannulation
  27090. heteroannulation
  27091. 5-ring
  27092. hypoiodite
  27093. alcohol
  27094. heteroannulations
  27095. heteroannulations
  27096. heteroar
  27097. heteroaromatic
  27098. heteroaromatic
  27099. bases
  27100. heteroaromatic
  27101. bases
  27102. nucleophilic
  27103. radicals
  27104. functionalization
  27105. heteroaromatic
  27106. systems
  27107. heteroatom
  27108. heterocumulenes
  27109. heterocy
  27110. heterocycle
  27111. heterocycle
  27112. heterocycle
  27113. imidazole
  27114. carbanion
  27115. alkylation
  27116. review
  27117. metal
  27118. heterocycle
  27119. review
  27120. alkaloid
  27121. pyrrolizidine
  27122. biology
  27123. bioche
  27124. heterocycle
  27125. synthesis
  27126. heterocycles
  27127. heterocycles
  27128. heterocycles
  27129. rearrangement
  27130. heterocycles
  27131. heterocyclic
  27132. heterocyclic
  27133. amines
  27134. heterocyclic
  27135. azadienes
  27136. dienophiles
  27137. derivatives
  27138. enamines
  27139. heterocyclic
  27140. compounds
  27141. heterocyclic
  27142. systems
  27143. marine
  27144. natural
  27145. products
  27146. heterodienophiles
  27147. heterodinuclear
  27148. heteroelement
  27149. heterogeneity
  27150. heterogeneous
  27151. heterogenous
  27152. heterolytic
  27153. heteroquadricyclanes
  27154. heteryne
  27155. hetring
  27156. hexabutylditin
  27157. hexacarbonyl
  27158. hexachlorocyclopenta
  27159. hexadiyne
  27160. hexafluoroantimonate
  27161. hexafluoroarsenate
  27162. hexahydrate
  27163. hexahydro
  27164. hexamethylenetetrami
  27165. hexamethylphosphoric
  27166. hexanediol
  27167. hexanes
  27168. hexanooxepin
  27169. hexatriene
  27170. hexen
  27171. hexene
  27172. hexenyl
  27173. hgcl2
  27174. hiadiazolothiadiazol
  27175. hickmott
  27176. hickmott
  27177. enamine
  27178. conjugation
  27179. nitrogen
  27180. synthesis
  27181. alkylation
  27182. hickmott
  27183. enamine
  27184. review
  27185. synthesis
  27186. chemistry
  27187. reaction
  27188. mechani
  27189. hickmott
  27190. review
  27191. enamine
  27192. conjugate
  27193. butadiene
  27194. butadienyl
  27195. dieny
  27196. hickmott
  27197. review
  27198. enamine
  27199. preparation
  27200. spectroscopy
  27201. alkylation
  27202. diastereofacial
  27203. selectivities
  27204. chelation
  27205. control
  27206. chiral
  27207. enantiomeric
  27208. purities
  27209. hydroxy
  27210. esters
  27211. optical
  27212. purity
  27213. alkyl
  27214. borabicyclo
  27215. 3.3.1
  27216. nonane
  27217. optical
  27218. purity
  27219. enantiomeric
  27220. purities
  27221. chiral
  27222. reduci
  27223. pressure
  27224. higher
  27225. higher
  27226. order
  27227. cuprate
  27228. higher
  27229. order
  27230. cuprate
  27231. addition
  27232. higher
  27233. order
  27234. cyano
  27235. cuprate
  27236. higher
  27237. order
  27238. hydrozirconation
  27239. transmetalation
  27240. alkenes
  27241. highly
  27242. highly
  27243. efficient
  27244. practical
  27245. approach
  27246. crystal
  27247. structure
  27248. carbon
  27249. highly
  27250. efficient
  27251. synthesis
  27252. analogs
  27253. highly
  27254. selective
  27255. reduction
  27256. silica
  27257. sodium
  27258. borohydride
  27259. highly
  27260. stereoselective
  27261. allylation
  27262. highly
  27263. stereoselective
  27264. synthesis
  27265. highly
  27266. stereoselective
  27267. synthesis
  27268. osmium
  27269. tetroxide
  27270. oxidation
  27271. hillman
  27272. hindered
  27273. hindered
  27274. rotation
  27275. radical
  27276. dipolar
  27277. cycloadditions
  27278. nitrile
  27279. hindrance
  27280. hiocins
  27281. hippocasine
  27282. hippodamine
  27283. hirai
  27284. hirai
  27285. lactam
  27286. review
  27287. cycloaddition
  27288. synthesis
  27289. biology
  27290. history
  27291. histrionicotoxin
  27292. histrionicotoxins
  27293. protease
  27294. inhibitor
  27295. peptide
  27296. isosteres
  27297. solid
  27298. phase
  27299. inhbitor
  27300. hixson
  27301. hixson
  27302. cyclopropane
  27303. photorearrangement
  27304. diradical
  27305. review
  27306. hiyama
  27307. review
  27308. heterocyclic
  27309. fragmentation
  27310. hoffman
  27311. hoffman
  27312. norbornadiene
  27313. thermal
  27314. rearrangement
  27315. extrusion
  27316. review
  27317. hoffman
  27318. tricarbonyl
  27319. preparation
  27320. review
  27321. writing
  27322. experimental
  27323. hoffmann
  27324. hoffmann
  27325. allyl
  27326. cation
  27327. equivalent
  27328. review
  27329. cycloaddition
  27330. diene
  27331. hoffmann
  27332. review
  27333. allyl
  27334. cation
  27335. butadiene
  27336. generation
  27337. cycloaddit
  27338. hoffmann
  27339. review
  27340. sigmatropic
  27341. theory
  27342. orbital
  27343. symmetry
  27344. heterocy
  27345. hofmann
  27346. holmes
  27347. holmes
  27348. cycloreversion
  27349. dipole
  27350. dipolar
  27351. review
  27352. writing
  27353. metathes
  27354. holton
  27355. holton
  27356. vinyl
  27357. carbanion
  27358. sulfur
  27359. enolate
  27360. cyclization
  27361. annulation
  27362. homoaldol
  27363. homoallyic
  27364. homoallyic
  27365. chiral
  27366. induction
  27367. homoallyl
  27368. homoallylic
  27369. homoallylic
  27370. homoallylic
  27371. alcohol
  27372. homoallylic
  27373. alcohol
  27374. synthesis
  27375. homoallylic
  27376. alcohols
  27377. homoallylic
  27378. amine
  27379. homoallylic
  27380. sulfides
  27381. homochiral
  27382. homochiral
  27383. rhodium
  27384. carboxylates
  27385. homocub
  27386. homocubanes
  27387. homoenolate
  27388. homoenolates
  27389. homogeneous
  27390. homogeneous
  27391. hydrogenation
  27392. complexes
  27393. homogeneously
  27394. homogenous
  27395. homologation
  27396. homologation
  27397. alcohol
  27398. metal
  27399. catalyst
  27400. carbon
  27401. monoxide
  27402. review
  27403. homologation
  27404. alkyl
  27405. ketones
  27406. alkynes
  27407. homolysis
  27408. homolytic
  27409. homophthalic
  27410. homoquinolizidine
  27411. silyl
  27412. silicon
  27413. ether
  27414. review
  27415. preparation
  27416. methodology
  27417. horner
  27418. horner
  27419. emmons
  27420. olefination
  27421. horner
  27422. emmons
  27423. reaction
  27424. horner
  27425. emmons
  27426. wadsworth
  27427. olefination
  27428. horner
  27429. emmons
  27430. wadsworth
  27431. reaction
  27432. horner
  27433. wittig
  27434. reaction
  27435. horner
  27436. wittig
  27437. reaction
  27438. stereoselective
  27439. synthesis
  27440. reduction
  27441. horner-emmons
  27442. horner-emmons
  27443. reaction
  27444. theory
  27445. calculations
  27446. physical
  27447. organic
  27448. pericyclic
  27449. concerted
  27450. review
  27451. cycloaddition
  27452. dipolar
  27453. review
  27454. ketone
  27455. photochem
  27456. alkene
  27457. methane
  27458. spectrosco
  27459. hoveyda
  27460. sulfinyl
  27461. anions
  27462. imines
  27463. alkaloids
  27464. review
  27465. huang-minlon
  27466. huang-minlon
  27467. reduction
  27468. ketone
  27469. hudlicky
  27470. hudlicky
  27471. alkaloid
  27472. pyrolizidine
  27473. review
  27474. azide
  27475. intramolecular
  27476. hueng
  27477. hueng
  27478. review
  27479. cyanide
  27480. nitrile
  27481. preparation
  27482. cyano
  27483. carbonyl
  27484. hughes
  27485. hughes
  27486. huisgen
  27487. huisgen
  27488. dipole
  27489. vinyl
  27490. electrocyclic
  27491. cyclization
  27492. review
  27493. orbita
  27494. huisgen
  27495. review
  27496. higher
  27497. order
  27498. cyclization
  27499. dipole
  27500. dipolar
  27501. elect
  27502. huisgen
  27503. thiocarbonyl
  27504. ylide
  27505. review
  27506. dipolar
  27507. cycloaddition
  27508. human
  27509. human
  27510. immunodeficiency
  27511. virus
  27512. facile
  27513. synthesis
  27514. carbovir
  27515. alkyl
  27516. hunsdiecker
  27517. preparation
  27518. hydrolysis
  27519. condensation
  27520. thioamide
  27521. oxidation
  27522. hutchins
  27523. hutchins
  27524. imine
  27525. amine
  27526. iminium
  27527. hydrazone
  27528. ketoxime
  27529. phosphinyl
  27530. silicon
  27531. review
  27532. steric
  27533. trimethyl
  27534. silyl
  27535. silyl
  27536. desilylation
  27537. hybridalactone
  27538. hydantocidin
  27539. hydrangenol
  27540. hydration
  27541. hydrazidoyl
  27542. hydrazine
  27543. hydrazoic
  27544. hydrazone
  27545. hydrazone
  27546. alkylation
  27547. hydrolysis
  27548. hydrazone
  27549. anion
  27550. hydrazone
  27551. carbanion
  27552. alkylation
  27553. hydrazones
  27554. hydrazonium
  27555. hydrazonium
  27556. addition
  27557. hydride
  27558. hydride
  27559. hydride
  27560. reduction
  27561. hydrides
  27562. hydridosilicates
  27563. hydrinadanone
  27564. hydrindan
  27565. hydrindan
  27566. palladium
  27567. catalyst
  27568. alkenic
  27569. cyclobutanol
  27570. expan
  27571. hydroalumination
  27572. hydroamination
  27573. hydroarylation
  27574. hydroazulene
  27575. hydroazulenes
  27576. hydroboration
  27577. hydrocarbon
  27578. hydrocarbons
  27579. hydrocarbonylation
  27580. hydrochloride
  27581. hydrochloride
  27582. hydrocyanation
  27583. hydrodesulfurization
  27584. hydrodesulfurization
  27585. hydroformylation
  27586. hydroformylation
  27587. catalytic
  27588. dinuclear
  27589. rhodium
  27590. regioselectiv
  27591. hydrofuran
  27592. hydrogen
  27593. addition
  27594. hydrogen
  27595. abstraction
  27596. hydrogen
  27597. peroxide
  27598. hydrogen
  27599. transfer
  27600. hydrogena
  27601. hydrogenation
  27602. hydrogenations
  27603. hydrogenolysis
  27604. hydrogens
  27605. hydrohalogenation
  27606. hydroisoquinolines
  27607. hydrolysis
  27608. hydrolysis
  27609. hydrolytic
  27610. hydromagnesiation
  27611. hydrometalation
  27612. hydrometallation
  27613. hydroperoxide
  27614. hydroperoxides
  27615. hydrophobic
  27616. hydrophosphonylation
  27617. hydroquinones
  27618. hydrosilane
  27619. hydrosilanes
  27620. hydrosilation
  27621. hydrosilylation
  27622. hydrostannation
  27623. hydrostannolysis
  27624. hydrostannylation
  27625. hydroxamic
  27626. hydroxide
  27627. hydroxy
  27628. hydroxy
  27629. aldehyde
  27630. hydroxy
  27631. alkene
  27632. hydroxy
  27633. amide
  27634. hydroxy
  27635. aromatic
  27636. compounds
  27637. dihydroxystyrene
  27638. derivatives
  27639. hydroxy
  27640. azide
  27641. alcohol
  27642. closure
  27643. aziridine
  27644. opening
  27645. hydroxy
  27646. carbonyl
  27647. compounds
  27648. hydroxy
  27649. dithioketal
  27650. cyclization
  27651. hydroxy
  27652. equivalent
  27653. reagents
  27654. hydroxy
  27655. ketone
  27656. hydroxy
  27657. lactam
  27658. hydroxy-ketone
  27659. hydroxyalkylation
  27660. hydroxyanthraquinone
  27661. hydroxyazetidines
  27662. hydroxybenzylation
  27663. hydroxycarbonyl
  27664. hydroxycarbonyl
  27665. derivatives
  27666. hydroxyimides
  27667. hydroxyl
  27668. hydroxyl
  27669. amine
  27670. oxidation
  27671. reagent
  27672. nitrone
  27673. perruthenate
  27674. hydroxyl
  27675. directed
  27676. hydroxyl
  27677. directed
  27678. hydrogenation
  27679. hydroxyl
  27680. functions
  27681. organic
  27682. synthesis
  27683. triethylsilane
  27684. protecti
  27685. hydroxylamine
  27686. hydroxylamine
  27687. retro
  27688. elimination
  27689. pyrrolidine
  27690. hydroxylamine-o-sulf
  27691. hydroxylamines
  27692. hydroxylated
  27693. hydroxylation
  27694. hydroxymethyl
  27695. hydroxymethyla
  27696. hydroxymethylation
  27697. hydroxymethylidene
  27698. hydroxymethylindole
  27699. hydroxyphenylsulfone
  27700. hydroxypyridines
  27701. hydroxysulfones
  27702. hydroylsis
  27703. hydrozirconation
  27704. hyperconjugation
  27705. hypercoordinate
  27706. hypercoordinate
  27707. organosilicon
  27708. compounds
  27709. organic
  27710. synthesis
  27711. hypervalent
  27712. hypervalent
  27713. iodine
  27714. diacetate
  27715. hydroxy
  27716. tosyloxy
  27717. hypobromous
  27718. hypochlorite
  27719. hypoiodite
  27720. hypoxanthines
  27721. hyride
  27722. hyroxy
  27723. hyroxy
  27724. synthesis
  27725. hysical
  27726. hysical
  27727. organic
  27728. reactive
  27729. intermediates
  27730. strained
  27731. molecules
  27732. i-bu2alteph
  27733. i-opr
  27734. i-pro
  27735. ibuka
  27736. ibuka
  27737. review
  27738. copper
  27739. cuprate
  27740. addition
  27741. eneone
  27742. conjugate
  27743. chiral
  27744. iddon
  27745. iddon
  27746. thiophene
  27747. cycloaddition
  27748. opening
  27749. photochem
  27750. carbene
  27751. identification
  27752. midates
  27753. imidazodiazaborines
  27754. imidazoimidazoles
  27755. imidazole
  27756. imidazole-1-carboxyl
  27757. imidazoles
  27758. imidazolidines
  27759. imidazolidinethione
  27760. imidazolines
  27761. imidazolophanes
  27762. imidazolothiazoles
  27763. imidazolotriazoles
  27764. imidazooxadiazines
  27765. imidazooxazines
  27766. imidazopyrazines
  27767. imidazopyridazines
  27768. imidazopyridines
  27769. imidazopyridines
  27770. imidazopyrimidines
  27771. imidazopyridazines
  27772. imida
  27773. imidazopyrimidines
  27774. imidazothiadiazines
  27775. imidazothiazines
  27776. imidazotriazines
  27777. imide
  27778. imide
  27779. reduction
  27780. asymmetric
  27781. acyliminium
  27782. precursor
  27783. lacto
  27784. imides
  27785. imidines
  27786. imido
  27787. imidoyl
  27788. imidoyl
  27789. radical
  27790. imine
  27791. imine
  27792. aldol
  27793. reaction
  27794. kylation
  27795. imine
  27796. ester
  27797. imine
  27798. formation
  27799. reduction
  27800. imine
  27801. lactam
  27802. preparation
  27803. carbanion
  27804. enolate
  27805. cycloaddition
  27806. imine
  27807. photochem
  27808. isomerization
  27809. abstraction
  27810. cyclization
  27811. imine
  27812. reduction
  27813. imines
  27814. iminium
  27815. iminium
  27816. iminium
  27817. rearrangement
  27818. iminium
  27819. acyliminium
  27820. amino
  27821. alkene
  27822. lactam
  27823. iminium
  27824. allylsilane
  27825. cyclization
  27826. iminium
  27827. cyclization
  27828. iminium
  27829. salts
  27830. trimethylsilanolate
  27831. sodium
  27832. deprotonation
  27833. iminiumether
  27834. imino
  27835. imino
  27836. reaction
  27837. iminoboranes
  27838. iminodiazonium
  27839. iminodithioles
  27840. iminoether
  27841. iminophosphorane
  27842. iminophosphorane
  27843. mediated
  27844. synthesis
  27845. electrocyclic
  27846. closu
  27847. iminophosphoranes
  27848. iminyl
  27849. iminyl
  27850. radicals
  27851. immonium
  27852. immunodeficiency
  27853. improvement
  27854. vitro
  27855. including
  27856. inclusion
  27857. increased
  27858. indacene
  27859. indanones
  27860. indazole
  27861. indazoles
  27862. indazoles
  27863. isoindazoles
  27864. pyrazolenines
  27865. isopyrazoles
  27866. pyrazoline
  27867. indazolines
  27868. indazolones
  27869. indene
  27870. indene
  27871. indenes
  27872. indenones
  27873. indirect
  27874. indium
  27875. indium
  27876. trichloride
  27877. indole
  27878. indole
  27879. acetic
  27880. acids
  27881. indole
  27882. glyoxylic
  27883. acids
  27884. analogs
  27885. indole
  27886. aziridine
  27887. opening
  27888. tryptophan
  27889. derivatives
  27890. lewis
  27891. indole
  27892. dimerization
  27893. indole
  27894. metalation
  27895. ndole
  27896. synthesis
  27897. nitro
  27898. aromatic
  27899. reduction
  27900. enamine
  27901. review
  27902. indole
  27903. coupling
  27904. palladium
  27905. introduction
  27906. stannane
  27907. indole-1-carboxylic
  27908. indoleacetic
  27909. indoleacetic
  27910. ester
  27911. indolene
  27912. indolenines
  27913. indoles
  27914. indoles
  27915. carbazoles
  27916. oindoles
  27917. indolizines
  27918. indoles
  27919. carbazoles
  27920. isoindoles
  27921. indolizines
  27922. indoles
  27923. route
  27924. indoline
  27925. indolization
  27926. indolizidine
  27927. indolizidine
  27928. alkaloid
  27929. pyrrole
  27930. reduction
  27931. reduction
  27932. friede
  27933. indolizidine
  27934. alkaloids
  27935. heteroaromatic
  27936. bases
  27937. acetate
  27938. indolizidine
  27939. alkaloids
  27940. intramolecular
  27941. cycloaddition
  27942. indolizidine
  27943. hydroxamic
  27944. oxidation
  27945. diene
  27946. cycloaddition
  27947. indolizidine
  27948. quinolizidine
  27949. swainsonine
  27950. castanospermine
  27951. azide
  27952. indolizidines
  27953. indolizines
  27954. indolizines
  27955. indolizidines
  27956. cyclazines
  27957. diazapyracyclenes
  27958. diaza
  27959. indolone
  27960. indoloquinone
  27961. induced
  27962. cyclizations
  27963. exocyclic
  27964. alkenes
  27965. alkyllithiums
  27966. alkynes
  27967. induced
  27968. epoxide
  27969. fragmentation
  27970. induction
  27971. induction
  27972. nitrogen
  27973. inductive
  27974. industrial
  27975. industry
  27976. inept
  27977. infrared
  27978. inhbitor
  27979. inhibition
  27980. inhibitor
  27981. inhibitors
  27982. inhibitors
  27983. protease
  27984. inhibitors
  27985. protease
  27986. alcohols
  27987. initiated
  27988. initiation
  27989. initio
  27990. injured
  27991. inner
  27992. inorganic
  27993. inosines
  27994. inositol
  27995. insectiside
  27996. insertion
  27997. insertion
  27998. isocyanide
  27999. zirconium
  28000. complex
  28001. inside
  28002. insitu
  28003. insoluble
  28004. intake
  28005. inter
  28006. interaction
  28007. interactions
  28008. intercalation
  28009. nterception
  28010. interchange
  28011. interconversion
  28012. intermediacy
  28013. intermediate
  28014. intermediates
  28015. intermediates
  28016. intermolecular
  28017. intermolecular
  28018. ionic
  28019. intramolcular
  28020. 15-c-h
  28021. insertion
  28022. reaction
  28023. intramolcular
  28024. diels-alder
  28025. intramolcular
  28026. wittig
  28027. reaction
  28028. intramolecular
  28029. intramolecular
  28030. intramolecular
  28031. cycloaddtion
  28032. intramolecular
  28033. photocycloaddition
  28034. building
  28035. blocks
  28036. cycloh
  28037. intramolecular
  28038. cycloaddition
  28039. intramolecular
  28040. cycloaddition
  28041. onylation
  28042. palladium
  28043. intramolecular
  28044. alkylation
  28045. intramolecular
  28046. allyl
  28047. silane
  28048. n-tosyliminium
  28049. cyclization
  28050. intramolecular
  28051. lithium
  28052. ester
  28053. rearrangement
  28054. intramolecular
  28055. chromium
  28056. complex
  28057. cyclization
  28058. intramolecular
  28059. cyclization
  28060. intramolecular
  28061. cyclization
  28062. alkaloid
  28063. intramolecular
  28064. cyclization
  28065. butyrolactones
  28066. dinoreudesman
  28067. intramolecular
  28068. cycloaddition
  28069. intramolecular
  28070. cyclopropanation
  28071. intramolecular
  28072. diels-alder
  28073. intramolecular
  28074. diels-alder
  28075. cycloaddition
  28076. intramolecular
  28077. dipolar
  28078. cycloaddition
  28079. intramolecular
  28080. intramolecular
  28081. friedel
  28082. crafts
  28083. reaction
  28084. intramolecular
  28085. functionalization
  28086. intramolecular
  28087. intramolecular
  28088. cyclization
  28089. transfer
  28090. intramolecular
  28091. hydrosilation
  28092. silafunctional
  28093. compounds
  28094. organi
  28095. intramolecular
  28096. etherification
  28097. intramolecular
  28098. michael
  28099. addtion
  28100. intramolecular
  28101. palladium
  28102. catalyzed
  28103. coupling
  28104. intramolecular
  28105. prins
  28106. intramolecular
  28107. pyridazine
  28108. diels
  28109. alder
  28110. extrusion
  28111. nitrogen
  28112. intramolecular
  28113. pyrylium
  28114. ylide
  28115. cycloaddition
  28116. intramolecular
  28117. schmidt
  28118. reaction
  28119. intramolecular
  28120. reformatsky
  28121. cyclization
  28122. intramolecular
  28123. alklyation
  28124. intramolecular
  28125. steric
  28126. interactions
  28127. intramolecular
  28128. trapping
  28129. alkyl
  28130. chloride
  28131. introductionE
  28132. introduction
  28133. introduction
  28134. weinreb
  28135. palladium
  28136. cascade
  28137. tandem
  28138. vinyl
  28139. introduction
  28140. writing
  28141. spiro
  28142. alkaloid
  28143. synthesis
  28144. review
  28145. perhydr
  28146. invention
  28147. inverse
  28148. inverse
  28149. demand
  28150. diels-alder
  28151. reaction
  28152. inverse
  28153. electron
  28154. demand
  28155. diels-alder
  28156. inversion
  28157. invitro
  28158. invitro
  28159. agents
  28160. involvement
  28161. iodide
  28162. introduction
  28163. iodide
  28164. elimination@
  28165. iodine@
  28166. iodophenol@
  28167. catalyzed
  28168. homologation
  28169. epoxide
  28170. carbonyl
  28171. rearrangement
  28172. iridium@
  28173. perchlorate@
  28174. isochromanones@
  28175. isokinetic@
  28176. isothiazole@
  28177. isothiazolines
  28178. isothiazolidines
  28179. isothiazolones
  28180. isothiazolino@
  28181. isoxazoles@
  28182. itsuno's
  28183. jenner@
  28184. jones
  28185. k-252d@
  28186. kanemasa
  28187. review
  28188. azomethine
  28189. ylide
  28190. azaallyl
  28191. anion
  28192. cycloaddit
  28193. kaup@
  28194. kellogg
  28195. dipole
  28196. azomethine
  28197. ylide
  28198. carbonyl
  28199. ylide
  28200. thiocarbonyl
  28201. ketals@
  28202. ester@
  28203. ketone
  28204. alkylation@
  28205. ketones
  28206. ketyl
  28207. radical@
  28208. kinetics
  28209. kishi
  28210. stereochem
  28211. osmium
  28212. oxidation
  28213. alkene
  28214. reagent
  28215. review@
  28216. kraus
  28217. enone
  28218. bridged
  28219. procedure
  28220. review
  28221. alkene
  28222. strain
  28223. synthesis@
  28224. kunz@
  28225. lactam
  28226. acetals@
  28227. lactones
  28228. lanthanide
  28229. bases@
  28230. mannich
  28231. cyclization
  28232. masked@
  28233. me3cok@
  28234. mechanisms
  28235. mercaptobenzoic@
  28236. metabolite
  28237. iodine
  28238. iodine
  28239. transfer
  28240. reaction
  28241. amination
  28242. iodoacetal
  28243. iodobenzaldehyde
  28244. iodobenzene
  28245. iodocyclization
  28246. iodocyclofunctionali
  28247. iodod
  28248. iodoetherification
  28249. iodoetherification
  28250. alcohol
  28251. alkene
  28252. tetrahydrofuran
  28253. iodofunctionalizatio
  28254. iodolactonization
  28255. iodonation
  28256. iodondium
  28257. iodonium
  28258. iodonium
  28259. dicollidine
  28260. perchlorate
  28261. iodotrimethylsilane
  28262. iodotrimethylsilane
  28263. sugar
  28264. lactones
  28265. catalyzed
  28266. homologation
  28267. epoxide
  28268. carbonyl
  28269. rearrangement
  28270. ion-radicals
  28271. ional
  28272. ionic
  28273. ionic
  28274. cycloaddition
  28275. ionization
  28276. ionized
  28277. ionomycin
  28278. ionomycin
  28279. ketones
  28280. ionophore
  28281. ionophores
  28282. ionophoric
  28283. borane
  28284. ireland
  28285. ireland
  28286. claisen
  28287. rearrangement
  28288. ireland
  28289. claisen
  28290. rearrangement
  28291. chloride
  28292. oxidation
  28293. perchlorate
  28294. phosphorus
  28295. carbonyl
  28296. carbene
  28297. cluster
  28298. crystal
  28299. structure
  28300. tricarbonyl
  28301. complexes
  28302. trichloride
  28303. iron-carbene
  28304. iron-carbene
  28305. methylenation
  28306. cyclopropane
  28307. di-iron
  28308. complexes
  28309. ironcarbonyl
  28310. irradiation
  28311. isatoic
  28312. isatonic
  28313. isobenzofuran
  28314. isocarbostyrils
  28315. isochromenes
  28316. isocomene
  28317. isocoumarin
  28318. isocoumarins
  28319. isocyanate
  28320. isocyanate/glycals/p
  28321. isocyanate/trichloro
  28322. isocyanates
  28323. isocyanide
  28324. isocyanides
  28325. isocyanides
  28326. cyanoacetic
  28327. arylglyoxal
  28328. anils
  28329. reaction
  28330. isocyanides
  28331. porphyrins
  28332. pyrroles
  28333. isocyanoacetate
  28334. isocyanocarboxylates
  28335. isocyanurates
  28336. isoflavenes
  28337. isoflavone
  28338. isogmelinol
  28339. isoguanines
  28340. isoindazoles
  28341. isoindole
  28342. isoindoles
  28343. isoiridomyrmecin
  28344. isokinetic
  28345. isokinetic
  28346. relationship
  28347. rates
  28348. isolation
  28349. isolaurepinnacin
  28350. isolaurepinnacin
  28351. systems
  28352. isomer
  28353. isomeric
  28354. isomerisation
  28355. isomerisations
  28356. isomerism
  28357. isomerization
  28358. isomerization
  28359. review
  28360. olefin
  28361. epoxide
  28362. thiirane
  28363. aziridine
  28364. alken
  28365. isomers
  28366. isonitrile
  28367. isopenicillin
  28368. isophorone
  28369. isopinocampheyl
  28370. isopinocampheyl
  28371. borane
  28372. isoprene
  28373. isoprenoids
  28374. isopropoxide
  28375. isopropyl
  28376. isopropyl
  28377. magnesium
  28378. bromide
  28379. isopyrazoles
  28380. isoquinoline
  28381. isoquinoline
  28382. metalation
  28383. isoquinolines
  28384. isoselective
  28385. isostere
  28386. isosteres
  28387. isosydnone
  28388. zolidines
  28389. isothiazolidinones
  28390. isothiazolines
  28391. isothiazolines
  28392. isothiazolidines
  28393. isothiazolones
  28394. isothiazolino
  28395. isothiazolinones
  28396. isothiazolones
  28397. isothiazolopyrazines
  28398. isothiazolopyridazin
  28399. isothiazolopyridines
  28400. isothiazolopyrimidin
  28401. isothiochroman
  28402. isothiochroman
  28403. anthraceno
  28404. thiopyran
  28405. isothiocyanate
  28406. isothiocyanates
  28407. isotope
  28408. isoureas
  28409. isoxazole
  28410. isoxazole
  28411. metalation
  28412. isoxazolidine
  28413. isoxazolidines
  28414. isoxazolidinium
  28415. isoxazoline
  28416. isoxazoline
  28417. spiro
  28418. derivatives
  28419. isoxazolines
  28420. isoxazoloisoxazoles
  28421. isoxazolophanes
  28422. isoxazolopyrazines
  28423. isoxazolopyridazines
  28424. isoxazolopyridines
  28425. isoxazolopyridines
  28426. isothiazolopyridines
  28427. oxazolopyridines
  28428. isoxazolopyrimidines
  28429. isoxazolothiadiazole
  28430. nickel
  28431. catalyst
  28432. cyclization
  28433. intramolecular
  28434. enyne
  28435. isonitr
  28436. itsuno's
  28437. itsuno's
  28438. itsuno's
  28439. reagent
  28440. ivermectin
  28441. michael
  28442. quinolizidine
  28443. indolizidine
  28444. alkaloid
  28445. review
  28446. jacobsen
  28447. jacobsen
  28448. epoxide
  28449. asymmetric
  28450. synthesis
  28451. writing
  28452. review
  28453. epoxida
  28454. jamison
  28455. jamison
  28456. jasperse
  28457. javanicus
  28458. jeffery
  28459. jeffery
  28460. conditions
  28461. pressure
  28462. diels
  28463. alder
  28464. pericyclic
  28465. jerina
  28466. jerina
  28467. shift
  28468. arene
  28469. oxide
  28470. hydrogen
  28471. biological
  28472. review
  28473. johnson
  28474. johnson
  28475. baldwin
  28476. rules
  28477. dunitz
  28478. trajectory
  28479. johnson
  28480. review
  28481. baldwin's
  28482. rules
  28483. stereoelectronic
  28484. johnson
  28485. radical
  28486. cation
  28487. writing
  28488. review
  28489. photochem
  28490. allene
  28491. elect
  28492. johnson
  28493. ylide
  28494. wittig
  28495. wittig
  28496. imino
  28497. phosphorane
  28498. alkene
  28499. johnstone
  28500. johnstone
  28501. review
  28502. hydrogenation
  28503. reduction
  28504. catalyst
  28505. experiment
  28506. jones
  28507. jones
  28508. jorgensen
  28509. jorgensen
  28510. diels
  28511. alder
  28512. dipolar
  28513. sigmatropic
  28514. electrocyclic
  28515. jorgensonI
  28516. jorgenson
  28517. computer
  28518. introduction
  28519. review
  28520. felkin
  28521. diastI
  28522. juaristi
  28523. juglone
  28524. julia
  28525. julia
  28526. coupling
  28527. julia
  28528. coupling
  28529. intramolecular
  28530. sulfone
  28531. target
  28532. reduction
  28533. cycli
  28534. julia-lythgoe
  28535. julia-lythgoe
  28536. coupling
  28537. junction
  28538. jurczak
  28539. jurczak
  28540. amino
  28541. hydroxy
  28542. acids
  28543. carbohydrate
  28544. serine
  28545. threonine
  28546. burgess
  28547. henderson
  28548. castanospermine
  28549. indolizidine
  28550. glycosida
  28551. kabalka
  28552. kabalka
  28553. pyrrole
  28554. alkene
  28555. nitrone
  28556. oxazole
  28557. review
  28558. nitro
  28559. heterocy
  28560. kagan
  28561. kagan
  28562. diels
  28563. alder
  28564. cycloaddition
  28565. chiral
  28566. catalytic
  28567. asymmetric
  28568. kainic
  28569. kainoids
  28570. kaliation
  28571. kametani
  28572. kametani
  28573. review
  28574. benzocyclobutene
  28575. quinone
  28576. methide
  28577. steroid
  28578. kanemasa
  28579. kanemasa
  28580. review
  28581. azomethine
  28582. ylide
  28583. azaallyl
  28584. anion
  28585. cycloaddit
  28586. kanemasa
  28587. review
  28588. azomethine
  28589. ylide
  28590. azaallyl
  28591. anion
  28592. cycloaddit
  28593. kanematsu
  28594. kanes
  28595. kapurimycins
  28596. karabatsos
  28597. kasai
  28598. kasai
  28599. mitomycin
  28600. target
  28601. aziridine
  28602. review
  28603. biology
  28604. cancer
  28605. kataoka
  28606. kataoka
  28607. sulfone
  28608. review
  28609. preparation
  28610. imine
  28611. sulfene
  28612. enamin
  28613. katritsky
  28614. katritsky
  28615. amine
  28616. leaving
  28617. group
  28618. methodology
  28619. review
  28620. displacemen
  28621. katritsky
  28622. azomethine
  28623. ylide
  28624. pyridinium
  28625. dipolar
  28626. cycloaddition
  28627. katritzky
  28628. katritzky
  28629. amine
  28630. pyrylium
  28631. cation
  28632. pyridinium
  28633. review
  28634. conversion
  28635. katritzky
  28636. sultam
  28637. review
  28638. sulfamyl
  28639. friedel
  28640. craft
  28641. katritzky
  28642. synthon
  28643. synthesis
  28644. review
  28645. amine
  28646. nitrogen
  28647. auxiliary
  28648. katritzky
  28649. ylide
  28650. pyridine
  28651. review
  28652. pyridinium
  28653. preparation
  28654. katsukiG
  28655. katsuki
  28656. chiral
  28657. epoxide
  28658. epoxidation
  28659. salen
  28660. manganese
  28661. asymmetriG
  28662. conditions
  28663. photorearrangement
  28664. review
  28665. benzene
  28666. fragmentation
  28667. aromati
  28668. keith
  28669. kellogg
  28670. kellogg
  28671. dipole
  28672. azomethine
  28673. ylide
  28674. carbonyl
  28675. ylide
  28676. thiocarbonyl
  28677. ketal
  28678. ketal
  28679. formation
  28680. ketal
  28681. synthesis
  28682. preparation
  28683. albizati
  28684. ketalization
  28685. ketene
  28686. acetal
  28687. ketene
  28688. cycloadditions
  28689. cyclohepatidenones
  28690. carbocations
  28691. rearra
  28692. ketene
  28693. dithioacetals
  28694. acetals
  28695. ketene
  28696. dithioacetals
  28697. organic
  28698. synthesis
  28699. reduction
  28700. ketene
  28701. dithioacetals
  28702. pyrimidine
  28703. derivatives
  28704. ketene
  28705. imine
  28706. thiocarbonyl
  28707. ketenes
  28708. ketenes
  28709. dimeric
  28710. reactions
  28711. nucleophiles
  28712. electrophile
  28713. ketenethioacetals
  28714. ketenimines
  28715. ketimine
  28716. ester
  28717. ketoacetals
  28718. ketoaldehyde
  28719. ketoester
  28720. ketoesters
  28721. ketohydrazone
  28722. ketone
  28723. ketone
  28724. triflate
  28725. palladium
  28726. coupling
  28727. vinyl
  28728. sulfide
  28729. ketone
  28730. reduction
  28731. ketone
  28732. synthesis
  28733. ketones
  28734. ketones
  28735. ketoxime
  28736. ketyl
  28737. ketyls
  28738. kf/h2o2
  28739. khand
  28740. khmds
  28741. kielbasinski
  28742. kielbasinski
  28743. carbodiimide
  28744. imide
  28745. review
  28746. esterification
  28747. reagen
  28748. kimpe
  28749. kinase
  28750. kinetic
  28751. kinetic
  28752. resolution
  28753. practical
  28754. method
  28755. kinetically
  28756. kinetically-controll
  28757. kinetics
  28758. kinetics
  28759. kinetics
  28760. reaction
  28761. rates
  28762. kinetics
  28763. catalysis
  28764. kinetics
  28765. heats
  28766. formation
  28767. kishi
  28768. kishi
  28769. hiyama
  28770. reaction
  28771. kishi
  28772. nozaki
  28773. hiyama
  28774. kishi
  28775. nozaki
  28776. reaction
  28777. ation
  28778. alkene
  28779. reagent
  28780. review
  28781. kishi
  28782. takai
  28783. nozaki
  28784. anhydride
  28785. synthesis
  28786. silicon
  28787. preparation
  28788. reagent
  28789. diacid
  28790. klein
  28791. klein
  28792. review
  28793. metalation
  28794. allylic
  28795. benzyl
  28796. carbanion
  28797. alkylation
  28798. klump
  28799. klump
  28800. review
  28801. heterocyclic
  28802. palladium
  28803. allyl
  28804. cyclization
  28805. kmno4
  28806. knoelker
  28807. knoelker
  28808. organoiron
  28809. alkaloid
  28810. review
  28811. knoevenagel
  28812. intramolecular
  28813. iminium
  28814. speckamp
  28815. cyclization
  28816. kolbe
  28817. koskinen
  28818. koskinen
  28819. review
  28820. asymmetric
  28821. synthesis
  28822. carbohydrates
  28823. kotali
  28824. kotali
  28825. kotha
  28826. kotsuki
  28827. krafft
  28828. kraus
  28829. kraus
  28830. enone
  28831. bridged
  28832. procedure
  28833. review
  28834. alkene
  28835. strain
  28836. synthesis
  28837. kraus
  28838. radical
  28839. review
  28840. cyclization
  28841. alkene
  28842. lactone
  28843. iodide
  28844. krief
  28845. krumpe
  28846. kuehne
  28847. kuehne
  28848. indole
  28849. alkaloid
  28850. review
  28851. biology
  28852. kuivila
  28853. kuivila
  28854. reduction
  28855. hydride
  28856. review
  28857. kulinkovich
  28858. kulinkovich
  28859. method
  28860. synthesis
  28861. quinoxaline
  28862. kuwajima
  28863. kuwajima
  28864. cyclopentane
  28865. zwitterion
  28866. silyl
  28867. ether
  28868. cyclop
  28869. kwart
  28870. kwart
  28871. temperature
  28872. review
  28873. isotope
  28874. deuterium
  28875. mechanism
  28876. glutamic
  28877. ester
  28878. boron
  28879. tribromide
  28880. catalytic
  28881. hydrogenation
  28882. l'abbe
  28883. l'abbe
  28884. heterocycle
  28885. rearrangement
  28886. dimroth
  28887. review
  28888. thermal
  28889. l'abbe
  28890. review
  28891. heterocycle
  28892. cyclopropane
  28893. heterocycle
  28894. rearrange
  28895. l'abbe
  28896. review
  28897. sulfur
  28898. conversion
  28899. heterocycle
  28900. l-aspartic
  28901. l-glutamic
  28902. l-malic
  28903. l-selectride
  28904. l-selectride
  28905. reduction
  28906. lablach
  28907. lablach
  28908. combier
  28909. azomethine
  28910. ylide
  28911. review
  28912. heteroaromatic
  28913. dipol
  28914. lactam
  28915. lactam
  28916. formation
  28917. lactam
  28918. opening
  28919. review
  28920. rearrangement
  28921. lactam
  28922. synthesis
  28923. lactams
  28924. lactarane
  28925. lactic
  28926. lactim
  28927. lactol
  28928. lactone
  28929. lactone
  28930. alkylation
  28931. lactone
  28932. deprotonation
  28933. lactone
  28934. formation
  28935. lactone
  28936. synthesis
  28937. lactones
  28938. lactones
  28939. lactonization
  28940. reduction
  28941. reduction
  28942. ester
  28943. experimental
  28944. metal
  28945. organometallic
  28946. review
  28947. technique
  28948. reage
  28949. magnesium
  28950. grignard
  28951. review
  28952. experimental
  28953. addition
  28954. activate
  28955. lambda
  28956. lanosterol
  28957. lanosterol
  28958. synthase
  28959. lanthanide
  28960. large
  28961. larock
  28962. laser
  28963. laser
  28964. flash
  28965. photolysis
  28966. hydrogen
  28967. migration
  28968. absolute
  28969. laser
  28970. photochemistry
  28971. hypervalent
  28972. iodine
  28973. molecular
  28974. oxygen
  28975. laszlo
  28976. laszlo
  28977. conversion
  28978. hydrolysis
  28979. ketone
  28980. hydrazone
  28981. catalyst
  28982. metal
  28983. latent
  28984. lates
  28985. lathi
  28986. laurencin
  28987. laurene
  28988. lavendamycin
  28989. lavendulae
  28990. lawesson
  28991. lawesson's
  28992. lawesson's
  28993. reagent
  28994. lawessons
  28995. deprotonation
  28996. tetraacetate
  28997. tetraacetate
  28998. dioximes
  28999. derivatives
  29000. complexes
  29001. kotali
  29002. lease
  29003. lease
  29004. review
  29005. strained
  29006. alkene
  29007. amide
  29008. bridgehead
  29009. least
  29010. leaving
  29011. leblanc
  29012. superoxide
  29013. review
  29014. oxygen
  29015. singlet
  29016. oxygen
  29017. electron
  29018. leffler
  29019. leffler
  29020. review
  29021. radical
  29022. electron
  29023. transfer
  29024. synthetic
  29025. leinamycin
  29026. length
  29027. lenoble
  29028. enamide
  29029. photorearrangement
  29030. cyclization
  29031. review
  29032. lepidine
  29033. leucomycin
  29034. leukotrienes
  29035. leusen
  29036. leusen
  29037. tosmic
  29038. isonitrile
  29039. carbanion
  29040. heterocycle
  29041. review
  29042. experi
  29043. levulinate
  29044. lewars
  29045. lewars
  29046. oxirene
  29047. preparation
  29048. review
  29049. small
  29050. heterocycle
  29051. lewis
  29052. lewis
  29053. lewis
  29054. catalyst
  29055. lewis
  29056. catalysts
  29057. homogeneous
  29058. catalysis
  29059. michael
  29060. reactions
  29061. lewis
  29062. catalyzed
  29063. addition
  29064. allylstannane
  29065. lewis
  29066. catalyzed
  29067. aldol
  29068. reaction
  29069. lewis
  29070. catalyzed
  29071. allyl
  29072. addition
  29073. lewis
  29074. catalyzed
  29075. cyclization
  29076. lewis
  29077. catalyzed
  29078. cycloaddition
  29079. lewis
  29080. catalyzed
  29081. cycloalkylation
  29082. lewis
  29083. catalyzed
  29084. diels-alder
  29085. reaction
  29086. lewis
  29087. catalyzed
  29088. michael
  29089. addition
  29090. lewis
  29091. catalyzed
  29092. sigmatropic
  29093. rearrangement
  29094. lewis
  29095. complex
  29096. lewis
  29097. cyclization
  29098. lewis
  29099. induced
  29100. cyclization
  29101. lewis
  29102. mediated
  29103. aldol
  29104. lewis
  29105. mediated
  29106. cyclization
  29107. lewis
  29108. mediated
  29109. glycosylation
  29110. lewis
  29111. mediated
  29112. polyene
  29113. cyclization
  29114. lewis
  29115. promoted
  29116. cyclization
  29117. lewis
  29118. radical
  29119. cyclization
  29120. stereochem
  29121. addition
  29122. allylatio
  29123. lewis
  29124. lewis
  29125. thiophenoxide
  29126. lewis
  29127. acids
  29128. lewis
  29129. alkaloid
  29130. amaryllidaceae
  29131. sceletium
  29132. review
  29133. lewis
  29134. review
  29135. amaryllidaceae
  29136. sceletium
  29137. alkaloids
  29138. lhmds
  29139. liald4
  29140. lialh
  29141. lialh2
  29142. lialh4
  29143. lialh4
  29144. liary
  29145. libf4
  29146. lications
  29147. liebeskind
  29148. liebman
  29149. liebman
  29150. cyclopropene
  29151. strain
  29152. review
  29153. small
  29154. cyclopropane
  29155. lifetimes
  29156. ligand
  29157. ligands
  29158. ligands
  29159. substitution
  29160. complexes
  29161. lignan
  29162. lignan
  29163. dihydrosesamin
  29164. organic
  29165. synthesis
  29166. annulation
  29167. route
  29168. lignans
  29169. lihmds
  29170. lihmds
  29171. dieckmann
  29172. cyclization
  29173. liica
  29174. limitation
  29175. linked
  29176. linoleate
  29177. linoleate
  29178. hydroperoxides
  29179. allylic
  29180. hydroperoxides
  29181. viscosity
  29182. lipase
  29183. shutz
  29184. lipshutz
  29185. cuprate
  29186. review
  29187. higher
  29188. order
  29189. nitrile
  29190. cyano
  29191. copper
  29192. lipshutz
  29193. organocopper
  29194. substitution
  29195. copper
  29196. conjugate
  29197. addition
  29198. liquid
  29199. liquid
  29200. chromatography
  29201. convenient
  29202. synthesis
  29203. decomposition
  29204. liskamp
  29205. liskamp
  29206. peptide
  29207. amino
  29208. review
  29209. conformationally
  29210. literature
  29211. lithiate
  29212. lithiate
  29213. metallation
  29214. chelation
  29215. heterocycle
  29216. alkylation
  29217. metal
  29218. lithiation
  29219. lithiation
  29220. ation
  29221. reagents
  29222. lithio
  29223. lithio
  29224. acetonitrile
  29225. lithioamine
  29226. lithioethyl
  29227. lithiopiperidine
  29228. lithiopyrrolidine
  29229. lithiosilane
  29230. lithiosilanes
  29231. lithium
  29232. lithium
  29233. ammonia
  29234. reduction
  29235. lithium
  29236. anion
  29237. lithium
  29238. biphenylide
  29239. lithium
  29240. carbanion
  29241. lithium
  29242. carbenoids
  29243. organic
  29244. synthesis
  29245. silacyclobutane
  29246. vinylsi
  29247. lithium
  29248. carbometallation
  29249. lithium
  29250. chloride
  29251. lithium
  29252. chloride
  29253. accelerated
  29254. lithium
  29255. compounds
  29256. derivatives
  29257. lithium
  29258. cyclpentadienide
  29259. lithium
  29260. diethyl
  29261. amide
  29262. lithium
  29263. diethyl
  29264. phosphite
  29265. lithium
  29266. enolate
  29267. lithium
  29268. n-cyclohexyl-n-isopr
  29269. lithium
  29270. c-c-m
  29271. lithium
  29272. naphthalenide
  29273. lithium
  29274. perchlorate
  29275. sphonate
  29276. lithium
  29277. reduction
  29278. lithium
  29279. tellurium
  29280. exchange
  29281. little
  29282. littoralis
  29283. liver
  29284. lkenes
  29285. lladium
  29286. llics
  29287. lobes
  29288. lobesia
  29289. locations
  29290. lockhoff
  29291. lockhoff
  29292. review
  29293. glycolipids
  29294. synthesis
  29295. properties
  29296. glycosphing
  29297. lohray
  29298. lohray
  29299. oxazaborolidine
  29300. catalysis
  29301. reduction
  29302. diels
  29303. alder
  29304. revie
  29305. lohray
  29306. review
  29307. cyclic
  29308. sulfates
  29309. sulfites
  29310. alkylation
  29311. epoxid
  29312. lolactonisation
  29313. review
  29314. silver
  29315. oxidation
  29316. rearrangement
  29317. cycloaddition
  29318. lopez
  29319. lophotoxin
  29320. lopropane
  29321. loracarbef
  29322. lossen
  29323. lounasmaa
  29324. lounasmaa
  29325. tamminen
  29326. tropane
  29327. alkaloids
  29328. review
  29329. temperature
  29330. temperature
  29331. autoxidation
  29332. electron
  29333. resonance
  29334. unsatur
  29335. temperature
  29336. matrices
  29337. lower
  29338. structure
  29339. lubineau
  29340. lubineau
  29341. water
  29342. solvent
  29343. hydrophobic
  29344. effect
  29345. aqueous
  29346. medium
  29347. lucchi
  29348. luche
  29349. luche
  29350. method
  29351. lukevics
  29352. lukevics
  29353. review
  29354. sonication
  29355. heterocycle
  29356. sound
  29357. alkylation
  29358. catalyst
  29359. catalysis
  29360. claisen
  29361. review
  29362. metal
  29363. lyase
  29364. lyngbya
  29365. lysine
  29366. reetz
  29367. amino
  29368. amine
  29369. aldehyde
  29370. chiral
  29371. review
  29372. m-c-c-c-m
  29373. m-c-c-m
  29374. m-c-c-x
  29375. m-c-m
  29376. macdonald
  29377. macdonald
  29378. alkaloid
  29379. writing
  29380. cancer
  29381. review
  29382. pyrazolidine
  29383. macomber
  29384. macomber
  29385. review
  29386. spectroscopy
  29387. teach
  29388. macor
  29389. macro
  29390. macrocycle
  29391. macrocycles
  29392. macrocyclic
  29393. macrocyclic
  29394. intramolecular
  29395. cyclization
  29396. macrocyclic
  29397. peptide
  29398. macrocyclisation
  29399. macrocyclization
  29400. carbon
  29401. monoxide
  29402. macrocyclization
  29403. amide
  29404. formation
  29405. macrocyclization
  29406. zearalenone
  29407. macrocylization
  29408. macrolactamization
  29409. macrolactonisation
  29410. macrolactonization
  29411. macrolactonization
  29412. yamaguchi
  29413. method
  29414. macrolide
  29415. macrolides
  29416. macronecine
  29417. madesclaire
  29418. magnesium
  29419. magnesium
  29420. bromide
  29421. magnesium
  29422. bromide
  29423. etherate
  29424. magnesium
  29425. magnesium
  29426. nitronate
  29427. magnesium
  29428. magnetic
  29429. magnetic
  29430. resonance
  29431. spectroscopy
  29432. molecular
  29433. orbital
  29434. calculatio
  29435. magnus
  29436. magnus
  29437. carbanion
  29438. sulfone
  29439. review
  29440. alkylation
  29441. magnusson
  29442. maier
  29443. maier
  29444. review
  29445. eneyne
  29446. bergman
  29447. diradical
  29448. trigger
  29449. aromatic
  29450. majetich
  29451. majetich
  29452. microwave
  29453. review
  29454. diels
  29455. alder
  29456. claisen
  29457. rearrangement
  29458. majuscula
  29459. malmberg
  29460. malmberg
  29461. writing
  29462. electrochem
  29463. review
  29464. amide
  29465. student
  29466. introducti
  29467. malonate
  29468. malonate
  29469. alkylation
  29470. malononitrile
  29471. mammalian
  29472. mander
  29473. manders
  29474. manders
  29475. reagent
  29476. manganeseG
  29477. manganese
  29478. complex
  29479. salen
  29480. complex
  29481. epoxidation
  29482. manganese
  29483. triacetate
  29484. manganese
  29485. triacetate
  29486. oxidation
  29487. mangrove
  29488. chrysanthemic
  29489. insectiside
  29490. cyclopropane
  29491. carboxylic
  29492. mannich
  29493. mannich
  29494. cyclization
  29495. mannich
  29496. cyclization
  29497. mannose
  29498. mannosidase
  29499. mannostatin
  29500. manzamine
  29501. marasmic
  29502. marcaccini
  29503. marcaccini
  29504. mariano
  29505. mariano
  29506. review
  29507. photochem
  29508. iminium
  29509. aromatic
  29510. silicon
  29511. electron
  29512. marine
  29513. marine
  29514. metabolites
  29515. halichondria
  29516. markovnikov
  29517. markovski
  29518. marples
  29519. marshall
  29520. marshall
  29521. review
  29522. stannane
  29523. lewis
  29524. allyl
  29525. addition
  29526. carbo
  29527. martin
  29528. martin
  29529. review
  29530. suzuki
  29531. coupling
  29532. cross
  29533. palladium
  29534. martin
  29535. review
  29536. alkaloid
  29537. writing
  29538. target
  29539. aldol
  29540. intramolecul
  29541. martin
  29542. review
  29543. aldehyde
  29544. ketone
  29545. coupling
  29546. titanium
  29547. carbanion
  29548. martin
  29549. review
  29550. proton
  29551. spectroscopy
  29552. maryanoff
  29553. maryanoff
  29554. iminium
  29555. alkaloid
  29556. cyclization
  29557. review
  29558. stere
  29559. masamune
  29560. masamune
  29561. cycloaddition
  29562. diels
  29563. alder
  29564. review
  29565. induction
  29566. asymmetr
  29567. masamune
  29568. review
  29569. asymmetric
  29570. synthesis
  29571. stereochem
  29572. chiral
  29573. induc
  29574. masked
  29575. matched
  29576. matched
  29577. double
  29578. asymmetric
  29579. induction
  29580. material
  29581. materials
  29582. mathias
  29583. mathias
  29584. review
  29585. conversion
  29586. ester
  29587. catalyst
  29588. dehydrogenatio
  29589. matic
  29590. mations
  29591. matrices
  29592. matrix
  29593. matsumoto
  29594. matsumoto
  29595. pressure
  29596. reaction
  29597. organic
  29598. synthesis
  29599. review
  29600. matteson
  29601. matteson
  29602. boron
  29603. review
  29604. ester
  29605. chiral
  29606. stereochem
  29607. hydroboration
  29608. mayer
  29609. mayoralH
  29610. mayoral
  29611. epoxide
  29612. epoxidation
  29613. metal
  29614. organometallic
  29615. catalyzed
  29616. mccpm
  29617. mcdonald
  29618. mcdonald
  29619. review
  29620. carbene
  29621. anion
  29622. radical
  29623. generation
  29624. chemistry
  29625. mckervey
  29626. mcmurry
  29627. mcmurry
  29628. coupling
  29629. mcomie
  29630. mcomie
  29631. protection
  29632. deprotection
  29633. review
  29634. carbonyl
  29635. diene
  29636. mcpba
  29637. mcpba
  29638. oxidation
  29639. mcquillin
  29640. mcquillin
  29641. parker
  29642. stephenson
  29643. transition
  29644. metal
  29645. organometa
  29646. mcscf
  29647. me2al
  29648. me2culi
  29649. me2nhcl
  29650. me3al
  29651. me3cok
  29652. me3sicn
  29653. me3sii
  29654. me3sin3
  29655. me3sisme
  29656. me3sisnbu3
  29657. me3sisnbu3
  29658. route
  29659. cyclopentanones
  29660. equivalents
  29661. me3snch2li
  29662. me3snli
  29663. me5cu3li2
  29664. mealybug
  29665. mechan
  29666. mechanics
  29667. mechanism
  29668. mechanisms
  29669. mechanisms
  29670. mechanisms
  29671. heterolytic
  29672. fragmentation
  29673. mechanistic
  29674. mechanistic
  29675. aspects
  29676. copper
  29677. hydride
  29678. methylene
  29679. furanone
  29680. mechanistic
  29681. study
  29682. media
  29683. mediated
  29684. mediated
  29685. total
  29686. synthesis
  29687. tricarbonyl
  29688. tetracarbonyliron
  29689. mediatory
  29690. medium
  29691. meerwein
  29692. meier
  29693. meier
  29694. review
  29695. wolff
  29696. rearrangement
  29697. diazo
  29698. ketone
  29699. ketene
  29700. metal
  29701. melamines
  29702. membered
  29703. membrane
  29704. menger
  29705. directionality
  29706. angle
  29707. transition
  29708. state
  29709. baldwin
  29710. review
  29711. menger
  29712. intramolecular
  29713. review
  29714. lactonization
  29715. enzyme
  29716. physical
  29717. meno2
  29718. mercaptobenzoic
  29719. mercaptobenzoic
  29720. mercaptobenzothiazol
  29721. mercuration
  29722. mercuric
  29723. mercuric
  29724. acetate
  29725. mercuric
  29726. oxide
  29727. mediated
  29728. cyclization
  29729. mercuric
  29730. trifluoroacetate
  29731. mercury
  29732. mercury
  29733. chloride
  29734. hgcl2
  29735. mercury
  29736. induced
  29737. cyclization
  29738. mercury
  29739. triflate
  29740. mercury
  29741. mediated
  29742. cyclization
  29743. mercury
  29744. mediated
  29745. pinacol
  29746. rearrangement
  29747. mercury
  29748. trifluoroacetata
  29749. merisation
  29750. merostabilization
  29751. merrifield
  29752. merrifield
  29753. resin
  29754. mesembranol
  29755. acylation
  29756. mesomeric
  29757. messeguer
  29758. messeguer
  29759. chemoselective
  29760. epoxidation
  29761. epoxide
  29762. oxidation
  29763. dioxi
  29764. mesylate
  29765. mesylate
  29766. displacement
  29767. retention
  29768. configuration
  29769. phosphate
  29770. elimination
  29771. stereochemistry
  29772. substitution
  29773. metabolite
  29774. metabolite
  29775. metabolites
  29776. metalF
  29777. metal
  29778. cyclization
  29779. palladium
  29780. review
  29781. alkyne
  29782. intramolec
  29783. metal
  29784. guest
  29785. cations
  29786. molecular
  29787. recognition
  29788. antitumor
  29789. antibiot
  29790. metal
  29791. halogen
  29792. exchange
  29793. gamma
  29794. unsaturated
  29795. esters
  29796. decarbo
  29797. metal
  29798. promoted
  29799. cyclization
  29800. formal
  29801. total
  29802. synthesis
  29803. formi
  29804. metal-carbene
  29805. metal-catalysed
  29806. metal-catalysis
  29807. metal-ene
  29808. metalation
  29809. metalation
  29810. reagents
  29811. lithium
  29812. metallacycle
  29813. metallacycles
  29814. metallacyclic
  29815. metallacyclic
  29816. alkenylketone
  29817. complexes
  29818. molecular
  29819. structure
  29820. metallacyclobutanes
  29821. metallacyclobutanes
  29822. metallacyclopentanes
  29823. metallacyclopentadi
  29824. metallacyclopentadie
  29825. metallacyclopentanes
  29826. metallati
  29827. metallation
  29828. metallic
  29829. metal
  29830. cyclization
  29831. palladium
  29832. review
  29833. alkyne
  29834. intramolec@
  29835. metal
  29836. ketene
  29837. complexes
  29838. gamma
  29839. unsaturated
  29840. esters
  29841. decarbo@
  29842. metallic
  29843. metallocyclopentane@
  29844. methodology
  29845. review
  29846. alkyne
  29847. synthesis
  29848. cyclopropane
  29849. salaun@
  29850. methylenation
  29851. chromium
  29852. chloride
  29853. reagents@
  29854. methyleneamino@
  29855. mical
  29856. michael
  29857. addition@
  29858. microwave@
  29859. migratory@
  29860. miscellaneous
  29861. mixed
  29862. anhydride@
  29863. mixed
  29864. metal
  29865. complexes
  29866. catalyzed
  29867. hydrosilylation
  29868. pyrrolizidin@
  29869. molander
  29870. samarium
  29871. iodide
  29872. diiodide
  29873. review@
  29874. molybdenum
  29875. morrison@
  29876. multipoint
  29877. control
  29878. bicyclic
  29879. alkenes
  29880. bicyclo
  29881. 2.2.1
  29882. heptanes
  29883. n-acyl@
  29884. n-subtituted@
  29885. nahmds@
  29886. naio4
  29887. oxidation@
  29888. reactions
  29889. prins
  29890. reaction
  29891. 13-dioxanes
  29892. hetring
  29893. diol@
  29894. amines
  29895. asymmetric
  29896. reduction
  29897. techniques
  29898. methods
  29899. stereochemistry@
  29900. diels
  29901. alder
  29902. asymmetric
  29903. review
  29904. catalysis
  29905. hetero
  29906. imine
  29907. alde@
  29908. metallic
  29909. metallics
  29910. metallo
  29911. metallo-ene
  29912. metallocene
  29913. metallocene
  29914. complexes
  29915. titanium
  29916. complexes
  29917. vinylidene
  29918. metallocenes
  29919. metallocyclobutene
  29920. metalloimine
  29921. metalloporphyrin
  29922. metals
  29923. metathasis
  29924. metathesis
  29925. review
  29926. nitrene
  29927. aromatic
  29928. cyclization
  29929. multiplicity
  29930. methane
  29931. methanol
  29932. methanolog
  29933. methanolysis
  29934. methide
  29935. methides
  29936. methiodide
  29937. method
  29938. methodology
  29939. methodology
  29940. review
  29941. alkyne
  29942. synthesis
  29943. cyclopropane
  29944. salaun
  29945. methods
  29946. methoxy
  29947. methoxy
  29948. phenylalkenyl
  29949. phenanthrene
  29950. carboxylates
  29951. photochemica
  29952. methoxyallene
  29953. methoxyamine
  29954. methoxycarbonyl
  29955. methoxyphenylalkenyl
  29956. methoxyphenylalkenyl
  29957. phenanthrenecarboxyl
  29958. photophysical
  29959. methoxypyridinium
  29960. methoxyselenenylatio
  29961. methyl
  29962. methyl
  29963. phenylsulfonyl
  29964. orthopropionate
  29965. homoenolate
  29966. anion
  29967. methyl
  29968. cerium
  29969. addition
  29970. ketone
  29971. methyl
  29972. ethers
  29973. cleavage
  29974. methyl
  29975. groups
  29976. methyl
  29977. lithium
  29978. methyl
  29979. triflate
  29980. methylamides
  29981. methylation
  29982. methylenation
  29983. methylenation
  29984. chromium
  29985. chloride
  29986. reagents
  29987. methylene
  29988. methylene
  29989. cyclopropane
  29990. necyclobutane
  29991. methylenecyclopentan
  29992. methylenecyclopenten
  29993. methylenecyclopropan
  29994. methylenetetrahydrof
  29995. methylether
  29996. methylide
  29997. methylides
  29998. methylimidazole
  29999. methylmandelate
  30000. methylmercury
  30001. methylnickel
  30002. methylphenyl
  30003. methylradicals
  30004. methylseleno
  30005. methyltetrahydropyra
  30006. methylthio
  30007. methylzinc
  30008. mevinic
  30009. mevinolin
  30010. meyer-schuster
  30011. meyers
  30012. meyers
  30013. formamidine
  30014. chelation
  30015. lithiate
  30016. carbanion
  30017. alkylation
  30018. mgbr2
  30019. mgbr2
  30020. mical
  30021. mical
  30022. micell
  30023. michael
  30024. michael
  30025. addition
  30026. michael
  30027. addition
  30028. stereochemical
  30029. control
  30030. ketoester
  30031. michael
  30032. condensation
  30033. michael
  30034. indolizidine
  30035. quinolizidine
  30036. alkaloid
  30037. review
  30038. michael
  30039. review
  30040. indolizidine
  30041. quinolizidine
  30042. slaframine
  30043. michael
  30044. reaction
  30045. michael
  30046. alkylation
  30047. enantioselective
  30048. synthesis
  30049. carbon
  30050. michael
  30051. conjugate
  30052. addition
  30053. micheal
  30054. micheal
  30055. reaction
  30056. microbial
  30057. microbial
  30058. oxidation
  30059. organic
  30060. synthesis
  30061. stereocontrolled
  30062. synth
  30063. micromonospora
  30064. microsomal
  30065. microwave
  30066. microwave
  30067. review
  30068. diels
  30069. alder
  30070. claisen
  30071. rearrangement
  30072. subst
  30073. microwave
  30074. spectrum
  30075. group
  30076. electronegativities
  30077. abinitio
  30078. calcul
  30079. midland
  30080. migration
  30081. milbemycins
  30082. mimetics
  30083. mimics
  30084. mines
  30085. minor
  30086. minor
  30087. groove
  30088. magnetic
  30089. resonance
  30090. nucleic
  30091. acids
  30092. minor
  30093. groove
  30094. miscell
  30095. miscellane
  30096. miscellaneo
  30097. miscellaneou
  30098. miscellaneous
  30099. miscellaneous
  30100. mitchell
  30101. mitchell
  30102. review
  30103. stille
  30104. coupling
  30105. organostannane
  30106. palladium
  30107. mitomycin
  30108. mitsunoba
  30109. mitsunoba
  30110. phosphorous
  30111. carbon
  30112. displacement
  30113. substitution
  30114. revie
  30115. mitsunobu
  30116. mitsunobu
  30117. alcohol
  30118. displacement
  30119. phosphorous
  30120. carboxylate
  30121. mitsunobu
  30122. coupling
  30123. mitsunobu
  30124. inversion
  30125. mitsunobu
  30126. review
  30127. alcohol
  30128. ester
  30129. azide
  30130. amide
  30131. mixed
  30132. mixed
  30133. metal
  30134. complexes
  30135. catalyzed
  30136. hydrosilylation
  30137. pyrrolizidin
  30138. calculations
  30139. oxidative
  30140. phenoxy
  30141. radical
  30142. cyclization
  30143. complexes
  30144. model
  30145. model
  30146. solutions
  30147. waste
  30148. water
  30149. chlorination
  30150. chloroaldimines
  30151. modeling
  30152. modeling
  30153. chemical
  30154. reactivity
  30155. molecular
  30156. orbital
  30157. methods
  30158. diast
  30159. models
  30160. models
  30161. modification
  30162. modified
  30163. modified
  30164. curtius
  30165. reaction
  30166. convenient
  30167. reagent
  30168. organic
  30169. synthes
  30170. moiety
  30171. moiseenkov
  30172. moiseenkov
  30173. pummerer
  30174. rearrangement
  30175. sulfide
  30176. review
  30177. molander
  30178. molander
  30179. review
  30180. samarium
  30181. lanthanide
  30182. radical
  30183. molander
  30184. samarium
  30185. iodide
  30186. diiodide
  30187. review
  30188. molecular
  30189. molecular
  30190. calculations
  30191. contraction
  30192. molecular
  30193. crystals
  30194. revision
  30195. contacts
  30196. radii
  30197. molecular
  30198. mechanics
  30199. molecular
  30200. mechanics
  30201. force
  30202. field
  30203. system
  30204. route
  30205. molecular
  30206. recognition
  30207. computer
  30208. simulations
  30209. stereoselectivity
  30210. molecular
  30211. recognition
  30212. solvents
  30213. molecular
  30214. structures
  30215. molecular
  30216. structures
  30217. crystal
  30218. structure
  30219. complexes
  30220. chloride
  30221. molecule
  30222. molecule
  30223. induced
  30224. radical
  30225. formation
  30226. molecules
  30227. molina
  30228. molina
  30229. intramolecular
  30230. azide
  30231. dipolar
  30232. cycloaddition
  30233. epoxide
  30234. molybdenum
  30235. molybdenum
  30236. molybdenum
  30237. carbene
  30238. molybdenum
  30239. carbene
  30240. complex
  30241. molybdenum
  30242. complex
  30243. protecting
  30244. group
  30245. monensin
  30246. monoene
  30247. monoesters
  30248. monofluorination
  30249. monoisopinocampheylb
  30250. monoisopinylcampheyl
  30251. monomethyl
  30252. monomorine
  30253. monosaccharides
  30254. monoterpene
  30255. monoxide
  30256. montmorillonite
  30257. moody
  30258. moody
  30259. review
  30260. carbazole
  30261. alkaloid
  30262. pyrone
  30263. diels
  30264. alder
  30265. retrosynt
  30266. moore
  30267. moore
  30268. ketene
  30269. cycloaddition
  30270. review
  30271. cyano
  30272. cyanoketene
  30273. metal
  30274. metathesis
  30275. review
  30276. cyclization
  30277. intramolecu
  30278. review
  30279. synthesis
  30280. asymmetric
  30281. natural
  30282. product
  30283. chiral
  30284. morphine
  30285. morphine
  30286. target
  30287. convergent
  30288. radical
  30289. aromatic
  30290. cyclization
  30291. morpholine
  30292. morpholine
  30293. synthesis
  30294. morrison
  30295. morrison
  30296. photochemical
  30297. switches
  30298. review
  30299. morrison
  30300. review
  30301. bichromophore
  30302. carbonyl
  30303. ketone
  30304. photochem
  30305. mosher
  30306. mossbauer
  30307. motherwell
  30308. motherwell
  30309. crich
  30310. review
  30311. radical
  30312. motion
  30313. motohashi
  30314. motohashi
  30315. moulines
  30316. molecular
  30317. orbital
  30318. calculations
  30319. organolithium
  30320. mukaiyama
  30321. mukaiyama
  30322. aldol
  30323. mukaiyama
  30324. aldol
  30325. reaction
  30326. mukaiyama
  30327. conversion
  30328. alcohol
  30329. ester
  30330. heterocycle
  30331. methodol
  30332. mukaiyama
  30333. michael
  30334. aldol
  30335. reaction
  30336. mukerjee
  30337. mukerjee
  30338. heterocycle
  30339. azlactone
  30340. review
  30341. carbanion
  30342. alkylation
  30343. mukerjee
  30344. lactam
  30345. azetidinone
  30346. review
  30347. synthesis
  30348. reaction
  30349. multihetero
  30350. multihetero
  30351. rearrangement
  30352. nitrones
  30353. alpha
  30354. amido
  30355. ketones
  30356. multiple
  30357. multiplet
  30358. multiplicity
  30359. multipoint
  30360. multipoint
  30361. control
  30362. bicyclic
  30363. alkenes
  30364. bicyclo
  30365. 2.2.1
  30366. heptanes
  30367. multispin
  30368. munchnone
  30369. mushrooms
  30370. mutagenesis
  30371. mycinolide
  30372. myo-inositol
  30373. myrrhine
  30374. substituted
  30375. benzotriazoles
  30376. regioselective
  30377. substitution
  30378. 4-methoxy-benzyl
  30379. 2-cyanopyridinium
  30380. hexafluoroantimonate
  30381. acyldihydropyridones
  30382. grignard
  30383. reagents
  30384. titanium
  30385. reagents
  30386. acyliminium
  30387. alkene
  30388. carbocation
  30389. cationic
  30390. cyclization
  30391. acyliminium
  30392. alkene
  30393. electrophilic
  30394. aromatic
  30395. substitution
  30396. acyliminium
  30397. cyclization
  30398. silane
  30399. oxindole
  30400. acyliminium
  30401. reaction
  30402. silane
  30403. palladium
  30404. cataly
  30405. alkylpyridinium
  30406. salts
  30407. alkaloid
  30408. synthesis
  30409. derivatives
  30410. alkylpyridinium
  30411. salts
  30412. indole
  30413. alkaloids
  30414. nucleophilic
  30415. additi
  30416. n-dimethylamino
  30417. o-dimethylhydroxylam
  30418. oxides
  30419. synthesis
  30420. nitration
  30421. orientation
  30422. dithieno
  30423. protected
  30424. hydroxy
  30425. pentenylamines
  30426. nitrogen
  30427. heterocycles
  30428. substituted
  30429. benzotriazoles
  30430. chemistry
  30431. substituted
  30432. pyrrolidin
  30433. castanospermine
  30434. triacetoxybo
  30435. n-acyl
  30436. n-acyliminium
  30437. n-alkyl
  30438. n-alkylpyridinium
  30439. n-bu3p
  30440. n-butyllithium
  30441. n-c-c-c-o
  30442. n-coo
  30443. n-cyclohexyl-n-isopr
  30444. n-dimethylamino
  30445. n-dithiocaroxylate
  30446. n-hydroxylamide
  30447. n-methyl
  30448. n-methylmorpholine
  30449. n-methylmorpholine
  30450. n-oxide
  30451. n-no2
  30452. n-nr2
  30453. n-oxide
  30454. n-phenyl
  30455. n-ring
  30456. n-so2cl
  30457. n-substituted
  30458. n-substituted
  30459. lactam
  30460. n-sulfinyl
  30461. sulfur
  30462. diimides
  30463. imino
  30464. dienophiles
  30465. nitros
  30466. thionitr
  30467. n-sulfinylamides
  30468. n-sulfonyliminium
  30469. n-tosyliminium
  30470. n-trifylimidazole
  30471. naalh2
  30472. nabh3cn
  30473. nabh4
  30474. naftion-h
  30475. nagai
  30476. nagai
  30477. naio4
  30478. oxidation
  30479. nakamura
  30480. nakamura
  30481. felkin
  30482. chelation
  30483. copper
  30484. diastereosele
  30485. naked
  30486. naltrexone
  30487. reactions
  30488. reactions
  30489. beckmann
  30490. rearrangement
  30491. elimination
  30492. fragmentat
  30493. reactions
  30494. formation
  30495. appendages
  30496. enolates
  30497. dieckm
  30498. reactions
  30499. formation
  30500. aromatics
  30501. chain
  30502. appendage
  30503. reactions
  30504. formation
  30505. aromatics
  30506. functionali
  30507. reactions
  30508. sulfones
  30509. extrusion
  30510. reactions
  30511. chapman
  30512. rearrangement
  30513. reactions
  30514. dakin-west
  30515. reaction
  30516. reactions
  30517. willgerodt
  30518. reaction
  30519. ch2-c
  30520. reactions
  30521. pericyclic
  30522. reactions
  30523. sigmatropic
  30524. arrangemen
  30525. reactions
  30526. physical
  30527. organic
  30528. functional
  30529. groups
  30530. preparatio
  30531. reactions
  30532. prins
  30533. reaction
  30534. 13-dioxanes
  30535. hetring
  30536. reactions
  30537. contraction
  30538. favorskii
  30539. rearrangement
  30540. reactions
  30541. ritter
  30542. reaction
  30543. reactions
  30544. thiele-winter
  30545. acetoxy
  30546. ation
  30547. naocl
  30548. naphthalene
  30549. naphthalene
  30550. catalyzed
  30551. lithiation
  30552. synthetic
  30553. applications
  30554. naphthalene
  30555. synthesis
  30556. naphthalenes
  30557. naphthalenide
  30558. naphthol
  30559. synthesis
  30560. naphthothiophenes
  30561. naphthotriazines
  30562. naphthyl
  30563. naphthyloxazolines
  30564. naphthyridines
  30565. napthalene
  30566. napthalene
  30567. synthesis
  30568. napthalene
  30569. synthesis
  30570. napthalenide
  30571. narasaka
  30572. narasimhan
  30573. narasimhan
  30574. aromatic
  30575. anion
  30576. lithiation
  30577. heterocycle
  30578. review
  30579. narasimhan
  30580. aromatic
  30581. ortho
  30582. heterocycle
  30583. carbanion
  30584. review
  30585. alkyl
  30586. natale
  30587. natale
  30588. nation
  30589. natta
  30590. natural
  30591. natural
  30592. natural
  30593. products
  30594. natural
  30595. sesbanimide
  30596. ellipticine
  30597. derivatives
  30598. tricyclic
  30599. nature
  30600. nazarov
  30601. nazarov
  30602. cyclization
  30603. nbu3snf
  30604. nbuli
  30605. nctional
  30606. nctionalisation
  30607. nd-sims
  30608. ndages
  30609. negishi
  30610. negishi
  30611. carbozirconation
  30612. negishi
  30613. organometallic
  30614. review
  30615. lithium
  30616. grignard
  30617. synthesis
  30618. negishi
  30619. zirconium
  30620. zircocene
  30621. complex
  30622. cyclization
  30623. heterocycle
  30624. nelson
  30625. nelson
  30626. bicyclic
  30627. amine
  30628. inversion
  30629. nitrogen
  30630. review
  30631. bicyclic
  30632. nenitzescu
  30633. nenizetscu
  30634. neocarzinostatin
  30635. neocarzinostatin
  30636. chromophore
  30637. mediated
  30638. aldol
  30639. reaction
  30640. neolignans
  30641. neopentylidene
  30642. neous
  30643. neral
  30644. neutral
  30645. neutrophil
  30646. newaz
  30647. newaz
  30648. synthesis
  30649. lactone
  30650. cyclization
  30651. methylene
  30652. methodology
  30653. newcomb
  30654. newkome
  30655. newkome
  30656. review
  30657. carbanion
  30658. heterocycle
  30659. amine
  30660. alkylation
  30661. hetero
  30662. newton
  30663. newton
  30664. heterocycle
  30665. mesoionic
  30666. review
  30667. dipole
  30668. zwitter
  30669. newton
  30670. review
  30671. mesoionic
  30672. dipole
  30673. dipolar
  30674. dipolar
  30675. cycloaddition
  30676. nh-oh
  30677. nh-so2
  30678. nh2-so2
  30679. nhme2
  30680. nicholas
  30681. nicholas
  30682. reaction
  30683. nickel
  30684. nickel
  30685. catalyst
  30686. nickel
  30687. catalyst
  30688. nickel
  30689. catalyzed
  30690. coupling
  30691. nickel
  30692. catalyzed
  30693. nickel
  30694. review
  30695. organonickel
  30696. nickel
  30697. chloride
  30698. nickel
  30699. coupling
  30700. nickel
  30701. cyclooctadiene
  30702. nickel
  30703. bromide
  30704. nickel-aluminium
  30705. nicl2
  30706. nicl2
  30707. nicolaou
  30708. nicolaou
  30709. enediyne
  30710. review
  30711. antitumor
  30712. calcheamicin
  30713. bergman
  30714. ninhydrin
  30715. niobium
  30716. nitidine
  30717. nitrate
  30718. nitrate
  30719. ester
  30720. fragmentation
  30721. alkoxy
  30722. radical
  30723. fragmentation
  30724. nitrate
  30725. esters
  30726. nitration
  30727. nitrene
  30728. nitrene
  30729. sigmatropic
  30730. rearrangement
  30731. stevens
  30732. review
  30733. diazo
  30734. nitrenes
  30735. nitrenium
  30736. nitrenoid
  30737. nitrido-mn
  30738. nitrido-mn
  30739. complex
  30740. nitril
  30741. nitrile
  30742. nitrile
  30743. dipole
  30744. review
  30745. sulfur
  30746. paton
  30747. nitrile
  30748. homologation
  30749. tructure
  30750. nitrile
  30751. oxides
  30752. preparation
  30753. nitro
  30754. alkene
  30755. reduction
  30756. chloro
  30757. nitrile
  30758. synthesis
  30759. nitrile
  30760. synthesis
  30761. amine
  30762. alkene
  30763. allyl
  30764. review
  30765. preparation
  30766. nitrile
  30767. ylides
  30768. nitriles
  30769. nitriles
  30770. ketones
  30771. nitrilimine
  30772. nitrilimines
  30773. nitrilium
  30774. nitro
  30775. nitro
  30776. alcohol
  30777. nitro
  30778. aldol
  30779. reactionmichael
  30780. addition
  30781. nitro
  30782. cyclo
  30783. olefins
  30784. nitroalkenes
  30785. nitroolefins
  30786. nitroketones
  30787. nitro
  30788. reduction
  30789. nitro
  30790. toluene
  30791. fluoride
  30792. unsaturated
  30793. michael
  30794. displacement
  30795. nitroacetates
  30796. nitroacetic
  30797. nitroaldol
  30798. nitroalkanes
  30799. nitroalkene
  30800. nitroalkenes
  30801. nitroalkenest
  30802. nitroallylic
  30803. nitroallylic
  30804. ester
  30805. nitrobenzene
  30806. nitrobenzenes
  30807. nitrocompound
  30808. nitrocyclohexanones
  30809. nitroenamines
  30810. nitrogen
  30811. nitrogen
  30812. bridgehead
  30813. compounds
  30814. pyrrolo
  30815. quinoline
  30816. nitrogen
  30817. cleavage
  30818. nitrogen
  30819. expansion
  30820. nitrogen
  30821. thiocarbonyl
  30822. systems
  30823. photochemical
  30824. reactions
  30825. thioen
  30826. nitroketones
  30827. nitrometane
  30828. nitromethane
  30829. nitromethane
  30830. addition
  30831. nitrone
  30832. chiral
  30833. asymmetric
  30834. dipolar
  30835. cycloaddition
  30836. diastereosel
  30837. nitrone
  30838. cycloadditions
  30839. nitrone
  30840. sugar
  30841. ribase
  30842. shikimic
  30843. biosynthetic
  30844. target
  30845. hydrogenat
  30846. nitrones
  30847. nitroolefins
  30848. nitropropanes
  30849. nitros
  30850. nitrosation
  30851. nitroso
  30852. nitroso
  30853. diels-alder
  30854. reaction
  30855. nitrosoalkenes
  30856. nitrosoalkynes
  30857. nitrosodisulfonat
  30858. nitrosonium
  30859. nitroxide
  30860. nitroxides
  30861. receptor
  30862. conversion
  30863. discovery
  30864. amides
  30865. spectroscopy
  30866. multiplet
  30867. first
  30868. order
  30869. coupling
  30870. constant
  30871. spectroscopy
  30872. selectivity
  30873. nobel
  30874. noels
  30875. noels
  30876. fischer
  30877. ligand
  30878. insertion
  30879. synthetic
  30880. review
  30881. carbene
  30882. nolate
  30883. nometallics
  30884. chelation
  30885. control
  30886. controlled
  30887. nucleophilic
  30888. additions
  30889. template
  30890. synthesis
  30891. ligands
  30892. non-chelation
  30893. nonactin
  30894. nonane
  30895. nonanes
  30896. nonchelation
  30897. nonconjugated
  30898. nonconjugated
  30899. chromophores
  30900. nonhebel
  30901. nonhebel
  30902. radical
  30903. cyclopropylmethyl
  30904. cyclopropylcarbinyl
  30905. nonstabilized
  30906. nonsymmetric
  30907. nopinone
  30908. norbornadiene
  30909. norbornadienes
  30910. norbornadienes
  30911. hexachlorocyclopenta
  30912. deltacyclenes
  30913. additions
  30914. norbornene
  30915. norbornene
  30916. hydroarylation
  30917. hydroamination
  30918. norbornenones
  30919. normajusculamide
  30920. norrish
  30921. norrish
  30922. cleavage
  30923. novel
  30924. novel
  30925. carbonyl
  30926. addition
  30927. novikov
  30928. novikov
  30929. nitro
  30930. alkene
  30931. cycloaddition
  30932. diene
  30933. diels
  30934. alder
  30935. prepara
  30936. noyori
  30937. noyori
  30938. asymmetric
  30939. hydrogenation
  30940. noyori
  30941. prostaglandin
  30942. enolate
  30943. enone
  30944. acetal
  30945. epoxide
  30946. organometa
  30947. noyori
  30948. review
  30949. organometallic
  30950. enantioselective
  30951. magnesium
  30952. nozaki
  30953. reaction
  30954. nozaki
  30955. reaction
  30956. nozazki
  30957. nsion
  30958. nso2cl
  30959. ntermediates
  30960. nuclear
  30961. nuclear
  30962. magnetic
  30963. resonance
  30964. nucleic
  30965. nucleophile
  30966. nucleophiles
  30967. nucleophilic
  30968. nucleophilic
  30969. nucleophilic
  30970. addition
  30971. nucleophilic
  30972. additions
  30973. nucleophilic
  30974. epoxide
  30975. opening
  30976. nucleophilic
  30977. opening
  30978. nucleophilic
  30979. solvent
  30980. assistance
  30981. inductive
  30982. charge
  30983. dispersal
  30984. nucleophilic
  30985. substitution
  30986. selectivity
  30987. principle
  30988. transition
  30989. nucleoside
  30990. nucleoside
  30991. derivatives
  30992. series
  30993. nucleosides
  30994. nucleotides
  30995. nucleus
  30996. chemistry
  30997. derivatives
  30998. agent
  30999. analogs
  31000. nugent
  31001. nugent
  31002. epoxide
  31003. acrylate
  31004. metal
  31005. lactone
  31006. review
  31007. opening
  31008. nysted
  31009. nysted
  31010. olefination
  31011. alkyl
  31012. ethers
  31013. active
  31014. secondary
  31015. amines
  31016. asymmetric
  31017. reduction
  31018. ganometallics
  31019. lithium
  31020. methylmandelate
  31021. mosher
  31022. method
  31023. stannyl
  31024. ketyls
  31025. radical
  31026. cyclization
  31027. trimethylsilyl
  31028. iodide
  31029. o-alkylation
  31030. o-dimethylhydroxylam
  31031. o-mesitylenesulfonyl
  31032. o-quinondimethane
  31033. oannulations
  31034. obafluorin
  31035. obrecht
  31036. obrecht
  31037. review
  31038. regioselectivity
  31039. alkyne
  31040. diene
  31041. dihydropyrone
  31042. obtaining
  31043. occurring
  31044. och2ch2och3
  31045. ochromycinone
  31046. octanes
  31047. octavalene
  31048. octenones
  31049. history
  31050. biography
  31051. conformation
  31052. history
  31053. biography
  31054. crown
  31055. ethers
  31056. philosophy
  31057. science
  31058. physical
  31059. organic
  31060. stereoc
  31061. strategies
  31062. theor
  31063. synthesis
  31064. strategies
  31065. theory
  31066. synthesis
  31067. synthons
  31068. strategies
  31069. theory
  31070. synthesis
  31071. umpolung
  31072. techniques
  31073. methods
  31074. techniques
  31075. methods
  31076. crown
  31077. ethers
  31078. techniques
  31079. methods
  31080. cycloaddition
  31081. bayli
  31082. techniques
  31083. methods
  31084. functional
  31085. polymers
  31086. techniques
  31087. methods
  31088. heterocycles
  31089. indole
  31090. techniques
  31091. methods
  31092. pressure
  31093. techniques
  31094. methods
  31095. insoluble
  31096. polym
  31097. suppo
  31098. techniques
  31099. methods
  31100. lanthanide
  31101. shift
  31102. techniques
  31103. methods
  31104. stereochemistry
  31105. techniques
  31106. methods
  31107. optical
  31108. resolution
  31109. techniques
  31110. methods
  31111. organic
  31112. polymers
  31113. protec
  31114. techniques
  31115. methods
  31116. phase
  31117. transfer
  31118. organome
  31119. techniques
  31120. methods
  31121. phase
  31122. transfer
  31123. phase
  31124. techniques
  31125. methods
  31126. polymers
  31127. techniques
  31128. methods
  31129. polymers
  31130. heterogeneous
  31131. techniques
  31132. methods
  31133. phase
  31134. transfer
  31135. techniques
  31136. methods
  31137. pyrolysis
  31138. thermolysis
  31139. techniques
  31140. methods
  31141. reagents
  31142. chiral
  31143. techniques
  31144. methods
  31145. sonication
  31146. techniques
  31147. methods
  31148. sonochemistry
  31149. techniques
  31150. methods
  31151. supporte
  31152. reagents
  31153. techniques
  31154. methods
  31155. ultrasound
  31156. oducts
  31157. officinalis
  31158. oganolithium
  31159. ogenic
  31160. oguni
  31161. diels
  31162. alder
  31163. asymmetric
  31164. review
  31165. catalysis
  31166. hetero
  31167. imine
  31168. oi-pr
  31169. oindoles
  31170. ojima
  31171. ojima
  31172. review
  31173. metal
  31174. transition
  31175. catalyzed
  31176. carbonylation
  31177. carbon
  31178. okamura
  31179. review
  31180. conformation
  31181. rotation
  31182. rotomer
  31183. physical
  31184. organic
  31185. nation
  31186. alkylation
  31187. polymerization
  31188. synthesis
  31189. polymer
  31190. reagent
  31191. review
  31192. silicon
  31193. trimethyl
  31194. silyl
  31195. iodide
  31196. cleavage
  31197. olefin
  31198. odonium
  31199. aziridine
  31200. review
  31201. chiral
  31202. metal
  31203. olefin
  31204. cyclization
  31205. olefin
  31206. cycloadditions
  31207. nitrile
  31208. oxides
  31209. olefin
  31210. metathesis
  31211. olefin
  31212. metathesis
  31213. vinylcarbene
  31214. complexes
  31215. alkylidene
  31216. complexe
  31217. olefin
  31218. silicon
  31219. alkene
  31220. peterson
  31221. alkoxide
  31222. review
  31223. stereochem
  31224. olefin
  31225. synthesis
  31226. olefin
  31227. synthesis
  31228. olefination
  31229. olefination
  31230. ketone
  31231. olefinic
  31232. olefinic
  31233. alcohol
  31234. olefinic
  31235. amine
  31236. olefinic
  31237. ketone
  31238. olefinic
  31239. nitrile
  31240. olefins
  31241. oligo
  31242. oligomerisation
  31243. oligomerizations
  31244. oligonucleotides
  31245. oligosaccaride
  31246. oligosaccharide
  31247. mesoionic
  31248. dipole
  31249. dipolar
  31250. cycloaddition
  31251. omega
  31252. ometallics
  31253. omplexes
  31254. onalisation
  31255. olefin
  31256. synthesis
  31257. oligosaccharides@
  31258. opening
  31259. openings@
  31260. optically
  31261. active
  31262. epoxides
  31263. episulfonium
  31264. nucleophilic
  31265. anometallics
  31266. lanthanides@
  31267. organic
  31268. organic
  31269. electrophiles
  31270. asymmetric
  31271. synthesis
  31272. organotin
  31273. reagent@
  31274. organic
  31275. synthesis
  31276. quinic
  31277. acid@
  31278. organnotin@
  31279. organoaluminum
  31280. organoaluminum
  31281. annulation@
  31282. organoboron
  31283. lewis
  31284. acid@
  31285. organolanthanide@
  31286. organolithium
  31287. acylation
  31288. carboxylate
  31289. cerium
  31290. ketone
  31291. formation@
  31292. organometallics
  31293. general
  31294. chemoselectivity@
  31295. organometallics
  31296. general
  31297. physical
  31298. organic@
  31299. organometallics
  31300. nucleophilic
  31301. addition
  31302. organometallics
  31303. lithium
  31304. protection
  31305. metallation
  31306. organometallics
  31307. mercury
  31308. organometallics
  31309. organic
  31310. synthesis
  31311. formation
  31312. enantio@
  31313. organometallics
  31314. palladium
  31315. formation
  31316. aromatics
  31317. heter@
  31318. organometallics
  31319. rhodium
  31320. stereochemistry
  31321. c-c-x
  31322. chiral
  31323. preparation
  31324. analogs
  31325. preparation
  31326. synthetic
  31327. lications
  31328. iminophospho
  31329. synthesis
  31330. carbonyl
  31331. compounds
  31332. catalyzed
  31333. synthesis
  31334. dibromide
  31335. synthesis
  31336. stereoselective
  31337. lithiation
  31338. entry
  31339. construction
  31340. cyclization
  31341. one-pot
  31342. onium
  31343. opane
  31344. opanones
  31345. chain
  31346. dienediyne
  31347. neocarzinostatin
  31348. chromophore
  31349. diene
  31350. transition
  31351. state
  31352. opening
  31353. opening
  31354. azabicyclic
  31355. cuprate
  31356. addition
  31357. opium
  31358. oppolzer
  31359. oppolzer
  31360. camphor
  31361. sultam
  31362. oppolzer
  31363. review
  31364. intramolecular
  31365. synthesis
  31366. thermal
  31367. sigmatr
  31368. oppolzer
  31369. intramolecular
  31370. cycloaddition
  31371. quinomethane
  31372. target
  31373. oppolzer
  31374. photocycloaddition
  31375. intramolecular
  31376. synthesis
  31377. oppolzer
  31378. review
  31379. diels
  31380. alder
  31381. dipolar
  31382. cycloaddition
  31383. dipole
  31384. oppolzer's
  31385. oppolzer's
  31386. chiral
  31387. sultam
  31388. oppolzers
  31389. oppolzers
  31390. chiral
  31391. sultam
  31392. diels
  31393. alder
  31394. reaction
  31395. cycloadditions
  31396. opposite
  31397. opropanation
  31398. optical
  31399. optically
  31400. optically
  31401. active
  31402. allylsilanes
  31403. transition
  31404. metal
  31405. complexes
  31406. optically
  31407. active
  31408. amine
  31409. optically
  31410. active
  31411. cyclopropene
  31412. surface
  31413. phase
  31414. isomeri
  31415. optically
  31416. active
  31417. epoxides
  31418. episulfonium
  31419. nucleophilic
  31420. ometallics
  31421. lanthanides
  31422. anometallics
  31423. titanium
  31424. general
  31425. orbital
  31426. order
  31427. nometallics
  31428. lithium
  31429. magnesium
  31430. ometallics
  31431. copper
  31432. organ
  31433. organ
  31434. metallics
  31435. lanthanides
  31436. organi
  31437. organic
  31438. organic
  31439. organic
  31440. organic
  31441. electrophiles
  31442. asymmetric
  31443. synthesis
  31444. organotin
  31445. reagent
  31446. organic
  31447. reactions
  31448. organic
  31449. sulfur
  31450. chemistry
  31451. derivatives
  31452. organic
  31453. synthesis
  31454. organic
  31455. synthesis
  31456. cyclization
  31457. electrophilic
  31458. substitution
  31459. organic
  31460. synthesis
  31461. acylsilanes
  31462. organic
  31463. synthesis
  31464. aldol
  31465. reactions
  31466. derivatives
  31467. lithium
  31468. organic
  31469. synthesis
  31470. alpha
  31471. epoxy
  31472. sulfoxides
  31473. sulfoxide
  31474. organic
  31475. synthesis
  31476. carboxylic
  31477. acids
  31478. organic
  31479. synthesis
  31480. cyclization
  31481. organic
  31482. synthesis
  31483. cyclization
  31484. diiodide
  31485. reduction
  31486. organic
  31487. synthesis
  31488. cycloadditions
  31489. nitrile
  31490. oxides
  31491. tetrahydrofu
  31492. organic
  31493. synthesis
  31494. cyclopropanes
  31495. derivatives
  31496. organic
  31497. synthesis
  31498. cleavage
  31499. neocarzinostatin
  31500. vinylallenes
  31501. organic
  31502. synthesis
  31503. hydrozirconation
  31504. transmetalation
  31505. vinylstan
  31506. organic
  31507. synthesis
  31508. manganese
  31509. acetate
  31510. substitution
  31511. organic
  31512. synthesis
  31513. nitroalkenes
  31514. dehydration
  31515. organic
  31516. synthesis
  31517. methylmandelate
  31518. practical
  31519. access
  31520. organic
  31521. synthesis
  31522. quinic
  31523. organic
  31524. synthesis
  31525. reagent
  31526. organic
  31527. synthesis
  31528. recognition
  31529. organic
  31530. synthesis
  31531. silylative
  31532. decarbonylation
  31533. convenient
  31534. organic
  31535. synthesis
  31536. solvents
  31537. enzymes
  31538. resolution
  31539. acetate
  31540. organic
  31541. synthesis
  31542. stereospecific
  31543. synthesis
  31544. directed
  31545. metalati
  31546. organic
  31547. synthesis
  31548. trimethylsilyldiazom
  31549. reagents
  31550. organic
  31551. synthesis
  31552. ultrasound
  31553. organic-reactions/cy
  31554. organism
  31555. organnostannane
  31556. annotin
  31557. organo
  31558. organo
  31559. etallics
  31560. palladium
  31561. organo
  31562. reagent
  31563. organo
  31564. lithium
  31565. organo
  31566. lithium
  31567. compounds
  31568. organo
  31569. lithium
  31570. compounds
  31571. barbier
  31572. carbonyl
  31573. compounds
  31574. organo
  31575. lithium
  31576. compounds
  31577. synthetic
  31578. applications
  31579. carbonyl
  31580. organo
  31581. lithium
  31582. reagents
  31583. organo
  31584. lithium
  31585. reagents
  31586. aldehydes
  31587. grignard
  31588. organo
  31589. stannane
  31590. organoaluminum
  31591. organoaluminum
  31592. annulation
  31593. organoaluminum
  31594. catalyst
  31595. organoaluminum
  31596. complex
  31597. organoaluminum
  31598. reagent
  31599. organobismuth
  31600. organoborane
  31601. organoboranes
  31602. organoborates
  31603. organoboron
  31604. organoboron
  31605. enolate
  31606. organoboron
  31607. hydride
  31608. organochromium
  31609. organocobalt
  31610. organocopp
  31611. organocopp
  31612. reagents
  31613. leaving
  31614. group
  31615. derivatives
  31616. alkylation
  31617. organocopper
  31618. organocopper
  31619. iodotrimethylsilane
  31620. claisen
  31621. rearrangement
  31622. gamma
  31623. organocopper
  31624. reagents
  31625. organocopper
  31626. reagents
  31627. allylic
  31628. derivatives
  31629. grignard
  31630. reagents
  31631. organocuprate
  31632. organofluorine
  31633. organofluorosilicate
  31634. organoiron
  31635. organoiron
  31636. complexes
  31637. organoiron
  31638. reagents
  31639. organic
  31640. synthesis
  31641. complexes
  31642. organolanthanide
  31643. organolithium
  31644. iamide
  31645. organolithium
  31646. enolate
  31647. organolithium
  31648. species
  31649. organolithiums
  31650. organom
  31651. organom
  31652. tallics
  31653. silicon
  31654. germanium
  31655. rearrangement
  31656. organomagnesium
  31657. organomanganese
  31658. organome
  31659. organome
  31660. allics
  31661. general
  31662. organome
  31663. allics
  31664. organome
  31665. allics
  31666. sulphur
  31667. substitution
  31668. organomercury
  31669. organomet
  31670. organomet
  31671. llics
  31672. titanium
  31673. zirconium
  31674. organometa
  31675. organometa
  31676. organometal
  31677. organometallicF
  31678. organometallic
  31679. organometallic
  31680. chemistry
  31681. crystal
  31682. structure
  31683. cluster
  31684. organometallic
  31685. reagents
  31686. derivatives
  31687. organometallic
  31688. reagents
  31689. chirality
  31690. transfer
  31691. grignard
  31692. reagents
  31693. organometallic
  31694. reagents
  31695. dialkylzinc
  31696. compounds
  31697. asymmetric
  31698. organometallics
  31699. organometallics
  31700. organometallics
  31701. organometallics
  31702. organometallics
  31703. aluminium
  31704. organometallics
  31705. aluminium
  31706. alkynes
  31707. acetylenes
  31708. carbometallatio
  31709. organometallics
  31710. aluminium
  31711. enantiogenic
  31712. chiral
  31713. auxiliary
  31714. organometallics
  31715. aluminium
  31716. oxiranes
  31717. diethylaluminium
  31718. 2266-tet
  31719. organometallics
  31720. antimony
  31721. organometallics
  31722. arsenic
  31723. antimony
  31724. bismuth
  31725. organometallics
  31726. arsenic
  31727. arsonium
  31728. ylides
  31729. organometallics
  31730. arsenic
  31731. organometallics
  31732. bismuth
  31733. organometallics
  31734. boron
  31735. alkenes
  31736. borane
  31737. hydroboration
  31738. organometallics
  31739. boron
  31740. organometallics
  31741. boron
  31742. borohydrides
  31743. organometallics
  31744. boron
  31745. organometallics
  31746. boron
  31747. coupling
  31748. organometallics
  31749. boron
  31750. haloboranes
  31751. organometallics
  31752. boron
  31753. iminoboranes
  31754. organometallics
  31755. boron
  31756. reagents
  31757. borane
  31758. organometallics
  31759. boron
  31760. rearrangement
  31761. organometallics
  31762. organometallics
  31763. arenetricarbonylchr
  31764. organometallics
  31765. arene
  31766. complexes
  31767. addition
  31768. organometallics
  31769. ironcarbonyl
  31770. complexes
  31771. organometallics
  31772. cadmium
  31773. organometallics
  31774. cadmium
  31775. mercury
  31776. organometallics
  31777. carbynes
  31778. organometallics
  31779. cerium
  31780. organometallics
  31781. chromium
  31782. formation
  31783. aromatics
  31784. chain
  31785. organometallics
  31786. chromium
  31787. formation
  31788. aromatics
  31789. organometallics
  31790. chromium
  31791. organometallics
  31792. chromium
  31793. carbenoids
  31794. cycloaddition
  31795. organometallics
  31796. chromium
  31797. organometallics
  31798. chromium
  31799. molybdenum
  31800. tungsten
  31801. titanium
  31802. reduct
  31803. organometallics
  31804. cobalt
  31805. alkynes
  31806. propargyl
  31807. cation
  31808. organometallics
  31809. cobalt
  31810. c-c-m
  31811. organometallics
  31812. cobalt
  31813. organometallics
  31814. cobalt
  31815. functional
  31816. groups
  31817. alkenes
  31818. alkynes
  31819. organometallics
  31820. cobalt
  31821. tetracarbonylhydroco
  31822. organometallics
  31823. cobalt
  31824. rhodium
  31825. organometallics
  31826. copper
  31827. c-c-x
  31828. carbometallation
  31829. organometallics
  31830. copper
  31831. alkynes
  31832. carbome
  31833. organometallics
  31834. copper
  31835. formation
  31836. appen
  31837. 14-addi
  31838. organometallics
  31839. copper
  31840. organometallics
  31841. copper
  31842. vinyloxiranes
  31843. organocopper
  31844. organometallics
  31845. copper
  31846. ethers
  31847. oxiranes
  31848. organometallics
  31849. copper
  31850. cc-c-x
  31851. carbometallation
  31852. organometallics
  31853. copper
  31854. organometallics
  31855. copper
  31856. organometallics
  31857. quinones
  31858. organometallics
  31859. element
  31860. cerium
  31861. organometallics
  31862. element
  31863. phosphorus
  31864. organometallics
  31865. element
  31866. samarium
  31867. organometallics
  31868. organometallics
  31869. diolefin
  31870. complexes
  31871. organometallics
  31872. neral
  31873. metal
  31874. carbonyl
  31875. complexes
  31876. organometallics
  31877. general
  31878. organometallics
  31879. general
  31880. organometallics
  31881. general
  31882. formation
  31883. appendages
  31884. 12-add
  31885. organometallics
  31886. general
  31887. organometallics
  31888. general
  31889. addition
  31890. organometallics
  31891. general
  31892. carbometallation
  31893. organometallics
  31894. general
  31895. carbyne
  31896. organometallics
  31897. general
  31898. etallocenes
  31899. organometallics
  31900. general
  31901. heterogenous
  31902. catalysis
  31903. organometallics
  31904. general
  31905. chemoselectivity
  31906. organometallics
  31907. general
  31908. organometallics
  31909. general
  31910. metallocenes
  31911. organometallics
  31912. general
  31913. oxidation
  31914. organometallics
  31915. general
  31916. ozone
  31917. organometallics
  31918. general
  31919. substitution
  31920. organometallics
  31921. general
  31922. organometallics
  31923. general
  31924. complexes
  31925. organometallics
  31926. general
  31927. carbenoid
  31928. carbenes
  31929. organometallics
  31930. general
  31931. carbenoids
  31932. transition
  31933. metal
  31934. carbene
  31935. organometallics
  31936. general
  31937. carbonylation
  31938. organometallics
  31939. general
  31940. homogeneously
  31941. catalysed
  31942. insertion
  31943. organometallics
  31944. general
  31945. kinetic
  31946. resolution
  31947. organometallics
  31948. general
  31949. mechanisms
  31950. alkohols
  31951. carbonylati
  31952. organometallics
  31953. general
  31954. metathesis
  31955. organometallics
  31956. general
  31957. nickel
  31958. palladium
  31959. rhodium
  31960. organometallics
  31961. general
  31962. organic
  31963. synthesis
  31964. alkynes
  31965. annulation
  31966. organometallics
  31967. general
  31968. photochemical
  31969. reactions
  31970. photochemist
  31971. organometallics
  31972. general
  31973. physical
  31974. organic
  31975. organometallics
  31976. general
  31977. physical
  31978. organic
  31979. reactive
  31980. intermedia
  31981. organometallics
  31982. general
  31983. physical
  31984. organic
  31985. stereochemistry
  31986. organometallics
  31987. general
  31988. physical
  31989. organic
  31990. stereochemistry
  31991. organometallics
  31992. general
  31993. halides
  31994. alkenes
  31995. alkyn
  31996. organometallics
  31997. general
  31998. rearrangement
  31999. organometallics
  32000. general
  32001. rearrangements
  32002. organometallics
  32003. general
  32004. tantalum
  32005. tungsten
  32006. metathesis
  32007. catalys
  32008. organometallics
  32009. general
  32010. organometallics
  32011. general
  32012. organotransition-met
  32013. redox
  32014. reacti
  32015. organometallics
  32016. general
  32017. tenes
  32018. organometallics
  32019. germanium
  32020. organometallics
  32021. iridium
  32022. organometallics
  32023. formation
  32024. appendages
  32025. enantioge
  32026. organometallics
  32027. enolates
  32028. alkylation
  32029. c-x-r
  32030. dihydro
  32031. organometallics
  32032. organometallics
  32033. molybdenum
  32034. organometallics
  32035. nucleophilic
  32036. addition
  32037. organometallics
  32038. lanthanides
  32039. organometallics
  32040. lanthanides
  32041. organometallics
  32042. lanthanides
  32043. electrophilic
  32044. transition
  32045. organometallics
  32046. lanthanides
  32047. organometallics
  32048. lanthanides
  32049. organic
  32050. synthesis
  32051. organometallics
  32052. lanthanides
  32053. stereochemistry
  32054. lanthanides
  32055. organometallics
  32056. organometallics
  32057. lithium
  32058. formation
  32059. aromatics
  32060. chain
  32061. organometallics
  32062. lithium
  32063. organometallics
  32064. lithium
  32065. organometallics
  32066. lithium
  32067. magnesium
  32068. organometallics
  32069. lithium
  32070. mechanism
  32071. metallation
  32072. organometallics
  32073. lithium
  32074. mechanism
  32075. carbenoids
  32076. organometallics
  32077. lithium
  32078. metallation
  32079. organometallics
  32080. lithium
  32081. organometallics
  32082. lithium
  32083. physical
  32084. organic
  32085. rearrangements
  32086. organometallics
  32087. lithium
  32088. potassium
  32089. c-c-m
  32090. organometallics
  32091. lithium
  32092. protection
  32093. metallation
  32094. organometallics
  32095. lithium
  32096. r-so2
  32097. sulfones
  32098. sulfoximides
  32099. organometallics
  32100. lithium
  32101. sodium
  32102. potassium
  32103. organometallics
  32104. magnesium
  32105. c-c-m
  32106. organometallics
  32107. magnesium
  32108. organometallics
  32109. magnesium
  32110. calcium
  32111. strontium
  32112. barium
  32113. organometallics
  32114. magnesium
  32115. carbometalation
  32116. organometallics
  32117. magnesium
  32118. hydrometallation
  32119. hydromagnesiat
  32120. organometallics
  32121. magnesium
  32122. mechanism
  32123. ketones
  32124. organometallics
  32125. magnesium
  32126. organometallics
  32127. magnesium
  32128. carbometallation
  32129. organometallics
  32130. magnesium
  32131. stereochemistry
  32132. carbometallat
  32133. organometallics
  32134. manganese
  32135. substitution
  32136. organometallics
  32137. alkenes
  32138. addition
  32139. organometallics
  32140. mercury
  32141. alkenes
  32142. addition
  32143. oxidation
  32144. organometallics
  32145. mercury
  32146. alkenes
  32147. 12-addition
  32148. reduc
  32149. organometallics
  32150. mercury
  32151. organometallics
  32152. mercury
  32153. carbenes
  32154. organometallics
  32155. mercury
  32156. electrophilic
  32157. substitution
  32158. organometallics
  32159. mercury
  32160. physical
  32161. organic
  32162. reactive
  32163. intermedia
  32164. organometallics
  32165. mercury
  32166. radicals
  32167. organometallics
  32168. di-grignard
  32169. reagents
  32170. metallacyclobutan
  32171. organometallics
  32172. molybdenum
  32173. organometallics
  32174. organometallics
  32175. nickel
  32176. c-c-m
  32177. organometallics
  32178. nickel
  32179. coupling
  32180. carbonylation
  32181. organometallics
  32182. nickel
  32183. functional
  32184. groups
  32185. reduction
  32186. catalytic
  32187. organometallics
  32188. nickel
  32189. organometallics
  32190. nickel
  32191. palladium
  32192. annulation
  32193. 5-ring
  32194. organometallics
  32195. nickel
  32196. palladium
  32197. coupling
  32198. alkenes
  32199. alkanes
  32200. organometallics
  32201. niobium
  32202. tantalum
  32203. organometallics
  32204. organic
  32205. synthesis
  32206. organometallics
  32207. organic
  32208. synthesis
  32209. ation
  32210. pericyc
  32211. organometallics
  32212. organic
  32213. synthesis
  32214. formation
  32215. appenda
  32216. organometallics
  32217. organic
  32218. synthesis
  32219. formation
  32220. enantio
  32221. organometallics
  32222. organic
  32223. synthesis
  32224. carbonylation
  32225. oxida
  32226. organometallics
  32227. organic
  32228. synthesis
  32229. carbometallation
  32230. organometallics
  32231. organic
  32232. synthesis
  32233. carbonylation
  32234. insertion
  32235. organometallics
  32236. organic
  32237. synthesis
  32238. chromium
  32239. organometallics
  32240. organic
  32241. synthesis
  32242. element
  32243. rhodium
  32244. c-c-x
  32245. organometallics
  32246. organic
  32247. synthesis
  32248. organometallics
  32249. organic
  32250. synthesis
  32251. palladium
  32252. organometallics
  32253. organic
  32254. synthesis
  32255. organometallics
  32256. organic
  32257. synthesis
  32258. stereochemist
  32259. enantiosel
  32260. organometallics
  32261. organic
  32262. synthesis
  32263. transmetallatio
  32264. organometallics
  32265. organic
  32266. synthesis
  32267. palladium
  32268. c-c-m
  32269. organometallics
  32270. lladium
  32271. organometallics
  32272. palladium
  32273. organometallics
  32274. palladium
  32275. formation
  32276. annulations
  32277. organometallics
  32278. palladium
  32279. formation
  32280. aromatics
  32281. chain
  32282. organometallics
  32283. palladium
  32284. formation
  32285. aromatics
  32286. heter
  32287. organometallics
  32288. palladium
  32289. halides
  32290. coupling
  32291. organometallics
  32292. palladium
  32293. ch-ch
  32294. butadiene
  32295. organometallics
  32296. palladium
  32297. ch-ch2-ocoo-r
  32298. ch-ch2-ocoo-
  32299. organometallics
  32300. palladium
  32301. coupling
  32302. organometallics
  32303. palladium
  32304. heteroannulation
  32305. acetals
  32306. organometallics
  32307. palladium
  32308. heteroannulations
  32309. 6-ring
  32310. 5-ring
  32311. organometallics
  32312. palladium
  32313. oxidation
  32314. organometallics
  32315. palladium
  32316. organometallics
  32317. palladium
  32318. organometallics
  32319. palladium
  32320. formation
  32321. appendages
  32322. organometallics
  32323. phosphorus
  32324. enantiogenic
  32325. reactions
  32326. stereochem
  32327. organometallics
  32328. phosphorus
  32329. organometallics
  32330. potassium
  32331. lithium
  32332. functional
  32333. groups
  32334. preparat
  32335. organometallics
  32336. reagents
  32337. organometallics
  32338. rhodium
  32339. iridium
  32340. organometallics
  32341. rhodium
  32342. organometallics
  32343. rhodium
  32344. stereochemistry
  32345. c-c-x
  32346. chiral
  32347. organometallics
  32348. ruthenium
  32349. organic
  32350. synthesis
  32351. c-o-r
  32352. organometallics
  32353. ruthenium
  32354. osmium
  32355. organometallics
  32356. ruthenium
  32357. organometallics
  32358. samarium
  32359. ytterbium
  32360. organometallics
  32361. selenium
  32362. vinyl
  32363. selenides
  32364. organometallics
  32365. selenium
  32366. organometallics
  32367. selenium
  32368. organometallics
  32369. selenium
  32370. oxidation
  32371. epoxidation
  32372. organometallics
  32373. selenium
  32374. tellurium
  32375. organometallics
  32376. selenium
  32377. tellurium
  32378. organometallics
  32379. selenium
  32380. tellurium
  32381. organometallics
  32382. silicon
  32383. c-c-m
  32384. organometallics
  32385. silicon
  32386. c-c-m
  32387. electrophilic
  32388. organometallics
  32389. silicon
  32390. organometallics
  32391. silicon
  32392. rearrangement
  32393. organometallics
  32394. silicon
  32395. carbring
  32396. c-o-m
  32397. silocyclopro
  32398. organometallics
  32399. silicon
  32400. functional
  32401. groups
  32402. preparations
  32403. alken
  32404. organometallics
  32405. silicon
  32406. functional
  32407. groups
  32408. protection
  32409. hydroxy
  32410. organometallics
  32411. silicon
  32412. organopseudohalosila
  32413. azidosilanes
  32414. organometallics
  32415. silicon
  32416. organosilicon
  32417. peroxides
  32418. organometallics
  32419. silicon
  32420. physical
  32421. organic
  32422. stereochemistry
  32423. organometallics
  32424. silicon
  32425. r3sih
  32426. organometallics
  32427. silicon
  32428. reagents
  32429. me3sicn
  32430. me3sii
  32431. me3sin3
  32432. organometallics
  32433. silicon
  32434. reagents
  32435. organometallics
  32436. silicon
  32437. rearrangement
  32438. organometallics
  32439. silicon
  32440. organometallics
  32441. silicon
  32442. organometallics
  32443. silicon
  32444. silatranes
  32445. organometallics
  32446. silicon
  32447. stereochemistry
  32448. organometallics
  32449. silicon
  32450. substitution
  32451. electrophilic
  32452. organometallics
  32453. silicon
  32454. boron
  32455. organometallics
  32456. silicon
  32457. c-c-m
  32458. organometallics
  32459. silver
  32460. organometallics
  32461. sodium
  32462. potassium
  32463. organometallics
  32464. synthesis
  32465. c-c-m
  32466. allylcomp
  32467. allylmetal
  32468. organometallics
  32469. silicon
  32470. functional
  32471. groups
  32472. protection
  32473. hydroxy@
  32474. organometallics
  32475. synthesis
  32476. formation
  32477. appendages
  32478. enan@
  32479. organometallics
  32480. tellurium
  32481. organometallics
  32482. titanium
  32483. zirconium
  32484. hafnium
  32485. organonickel
  32486. catalyst@
  32487. organopalladium@
  32488. organopalladium
  32489. catalyst@
  32490. organoruthenium
  32491. catalyst@
  32492. organostannane
  32493. organostannanes@
  32494. organosulphur
  32495. organotin
  32496. reagent@
  32497. organozircoium@
  32498. p'-di-tert-butylphen@
  32499. palladium
  32500. palladium
  32501. asymmetric
  32502. silylation@
  32503. palladium
  32504. catalyzed
  32505. intramolecular
  32506. cyclization@
  32507. palladium
  32508. cyclization@
  32509. parnes
  32510. silicon
  32511. lewis
  32512. allyl
  32513. silyl
  32514. review
  32515. desilylation
  32516. pentane@
  32517. pericyclic
  32518. peters
  32519. lanthanide
  32520. shift
  32521. review
  32522. structure
  32523. determination@
  32524. phase
  32525. transfer
  32526. catalysis
  32527. coupling
  32528. reactions
  32529. organic
  32530. halides@
  32531. phenyl@
  32532. phosphorous
  32533. review
  32534. wittig
  32535. reagent
  32536. conditions
  32537. experimental
  32538. abramovitch@
  32539. boeckman@
  32540. merlic@
  32541. noels
  32542. graziani
  32543. hubert
  32544. schlosser
  32545. desponds
  32546. lehmann
  32547. moret
  32548. rauchschwalbe
  32549. weber
  32550. toner
  32551. goldberg
  32552. vogtle
  32553. laidler
  32554. stoddart
  32555. comprehensive
  32556. organic
  32557. synthesis@
  32558. promoted@
  32559. allene
  32560. ester
  32561. halide
  32562. cross
  32563. coupling
  32564. palladium
  32565. boron
  32566. suzuki
  32567. aziridine
  32568. review
  32569. preparation
  32570. imine
  32571. silyl
  32572. silicon
  32573. addition
  32574. butenolides
  32575. seiridium
  32576. cardinale
  32577. reagents@
  32578. formation
  32579. appendages
  32580. enolates
  32581. isocyanid@
  32582. carbohydrates@
  32583. copper
  32584. acetylacetonate/mono
  32585. peroxydicarbonates@
  32586. diels
  32587. alder
  32588. reaction
  32589. reagent@
  32590. nctional
  32591. groups
  32592. biotransformations
  32593. vitamin
  32594. functional
  32595. groups
  32596. preparations
  32597. heteroalkenes
  32598. nitroenamines@
  32599. glucose/asymmetric@
  32600. introduction@
  32601. metal
  32602. cyclization
  32603. palladium
  32604. review
  32605. alkyne
  32606. intramolec@
  32607. olefin
  32608. synthesis@
  32609. organometallics
  32610. silicon
  32611. functional
  32612. groups
  32613. protection
  32614. hydroxy
  32615. organometallics
  32616. silicon
  32617. functional
  32618. groups
  32619. protection
  32620. hydroxy@
  32621. ortho@
  32622. palladium
  32623. asymmetric
  32624. silylation@
  32625. photochemical
  32626. annulation@
  32627. phthalide@
  32628. potassium
  32629. cyanide@
  32630. potential
  32631. sialidase
  32632. inhibitors
  32633. alpha
  32634. glucosidase
  32635. inhibitors
  32636. proline
  32637. derivative
  32638. decarboxylation
  32639. iminium
  32640. mannich
  32641. pyrrolidine@
  32642. reagent
  32643. benzenedisulfonimide
  32644. monofluorination
  32645. methodology@
  32646. epimerization
  32647. secondary
  32648. hydroxyl
  32649. group@
  32650. syn/anti
  32651. ratio
  32652. dependent
  32653. lewis
  32654. acid@
  32655. treatment
  32656. butyldimethylsilyl
  32657. triethylsilyloxymet@
  32658. 2-aryl-4methylenetet@
  32659. general
  32660. synthesis
  32661. substituted
  32662. cyclohex
  32663. enones@
  32664. review
  32665. frank
  32666. phosphorus
  32667. sulphur
  32668. review
  32669. black
  32670. preparation
  32671. reactions
  32672. diazomet@
  32673. review
  32674. cooper
  32675. ginos
  32676. meister
  32677. synthesis
  32678. prop@
  32679. review
  32680. synth
  32681. optical
  32682. organometallics
  32683. synthesis
  32684. formation
  32685. appendages
  32686. organometallics
  32687. synthesis
  32688. organometallics
  32689. synthesis
  32690. addition
  32691. organometallics
  32692. synthesis
  32693. carbonylation
  32694. fischer-tropsch
  32695. organometallics
  32696. synthesis
  32697. organometallics
  32698. synthesis
  32699. organometallics
  32700. synthesis
  32701. chromium
  32702. carbenes
  32703. p-quinones
  32704. organometallics
  32705. synthesis
  32706. carbonylation
  32707. organometallics
  32708. synthesis
  32709. enantiogenic
  32710. reactions
  32711. stereochemi
  32712. organometallics
  32713. synthesis
  32714. heterocycles
  32715. organometallics
  32716. synthesis
  32717. hydrogenation
  32718. metallation
  32719. organometallics
  32720. synthesis
  32721. reduction
  32722. insertion
  32723. resctions
  32724. organometallics
  32725. synthesis
  32726. metal
  32727. carbonyls
  32728. organometallics
  32729. synthesis
  32730. nickel
  32731. palladium
  32732. organometallics
  32733. synthesis
  32734. selenium
  32735. ylides
  32736. annula
  32737. organometallics
  32738. synthesis
  32739. target
  32740. synthesis
  32741. natural
  32742. produ
  32743. organometallics
  32744. synthesis
  32745. catalysts
  32746. carbonylation
  32747. organometallics
  32748. tellurium
  32749. organometallics
  32750. tellurium
  32751. organometallics
  32752. thallium
  32753. formation
  32754. aromatics
  32755. organometallics
  32756. thallium
  32757. organometallics
  32758. metallation
  32759. alkynes
  32760. organometallics
  32761. diols
  32762. esterification
  32763. organometallics
  32764. me3snli
  32765. me3snch2li
  32766. sn-li
  32767. organometallics
  32768. physical
  32769. organic
  32770. mechanisms
  32771. organometallics
  32772. organometallics
  32773. organometallics
  32774. organometallics
  32775. titanium
  32776. formation
  32777. appendages
  32778. enant
  32779. organometallics
  32780. titanium
  32781. coupling
  32782. deoxygenation
  32783. organometallics
  32784. titanium
  32785. coupling
  32786. pinacol
  32787. deoxygenation
  32788. organometallics
  32789. titanium
  32790. functional
  32791. groups
  32792. preparations
  32793. organometallics
  32794. titanium
  32795. metal-carbene
  32796. complexes
  32797. cp2tich2
  32798. organometallics
  32799. titanium
  32800. organometallics
  32801. titanium
  32802. carbring
  32803. c-c-x
  32804. organometallics
  32805. titanium
  32806. zirconium
  32807. hafnium
  32808. organometallics
  32809. titanium
  32810. zirconium
  32811. hafnium
  32812. carbenoids
  32813. organometallics
  32814. titanium
  32815. zirconium
  32816. hafnium
  32817. organometallics
  32818. titanium
  32819. zirconium
  32820. organometallics
  32821. organometallics
  32822. tungsten
  32823. molybdenum
  32824. organometallics
  32825. cadmium
  32826. mercury
  32827. copper
  32828. silver
  32829. organometallics
  32830. organometallics
  32831. onium
  32832. organometallics
  32833. zirconium
  32834. formation
  32835. annulation
  32836. organometallics
  32837. zirconium
  32838. annulation
  32839. carbometallation
  32840. organometallics
  32841. zirconium
  32842. carbonylation
  32843. organometallics
  32844. zirconium
  32845. hafnium
  32846. organometallics
  32847. zirconium
  32848. hydrometallation
  32849. organometallics
  32850. zirconium
  32851. organometallics
  32852. zirconium
  32853. organometals
  32854. organomolybdenum
  32855. organonickel
  32856. organopalladium
  32857. ophosphorous
  32858. organoplatinum
  32859. organopseudohalosila
  32860. organorhodium
  32861. organorhodium
  32862. catalyst
  32863. organorhodium
  32864. complex
  32865. organoruthenium
  32866. organoruthenium
  32867. catalyst
  32868. organoruthenium
  32869. complex
  32870. organoruthenium
  32871. ruthenium
  32872. complex
  32873. organoruthenium
  32874. transition
  32875. metal
  32876. complex
  32877. organoselenium
  32878. organosilane
  32879. organosilicon
  32880. organosilicon
  32881. chemistry
  32882. organosilicon
  32883. compounds
  32884. organic
  32885. halides
  32886. reagent
  32887. organosodium
  32888. organostannane
  32889. organosulphur
  32890. organotellurium
  32891. organotellurium
  32892. species
  32893. organotin
  32894. organotin
  32895. chemistry
  32896. organotin
  32897. enolate
  32898. organotin
  32899. hydride
  32900. reagent
  32901. organotin
  32902. reagents
  32903. oxidative
  32904. addition
  32905. organic
  32906. halides
  32907. pallad
  32908. organotitanium
  32909. organotitanium
  32910. catalyst
  32911. organotitanium
  32912. complex
  32913. organotitanium
  32914. hyride
  32915. reduction
  32916. organotitanium
  32917. reagent
  32918. organotitanium
  32919. reduction
  32920. organotitanuim
  32921. organotransition-met
  32922. organotungsten
  32923. organotungsten
  32924. complex
  32925. organozinc
  32926. organozinc
  32927. bromide
  32928. organozinc
  32929. reagent
  32930. ortho
  32931. ortho
  32932. acylation
  32933. ortho
  32934. alkenyl
  32935. isonitrile
  32936. hydride
  32937. alpha
  32938. stannylimido
  32939. ortho
  32940. ester
  32941. ortho
  32942. esters
  32943. hydrolysis
  32944. ortho
  32945. metalation
  32946. reactions
  32947. organic
  32948. synthesis
  32949. chain
  32950. reactions
  32951. ortho-aminoaldehydes
  32952. orthocarbamil
  32953. orthocarbonic
  32954. orthoester
  32955. orthoesters
  32956. orthopropionate
  32957. orton
  32958. oselective
  32959. osmium
  32960. osmium
  32961. tetroxide
  32962. smium
  32963. tetroxide
  32964. oxidation
  32965. ether
  32966. osmylation
  32967. oso4-cinchona
  32968. oso4-cinchona
  32969. alkaliod
  32970. catalyst
  32971. osure
  32972. other
  32973. others
  32974. outer
  32975. outside
  32976. ovens
  32977. overman
  32978. overman
  32979. cation
  32980. cyclization
  32981. alkaloid
  32982. review
  32983. writing
  32984. iminium
  32985. overman
  32986. cationic
  32987. cyclizations
  32988. review
  32989. ketene
  32990. rearrangement
  32991. shift
  32992. imine
  32993. cycloaddition
  32994. flash
  32995. oxaannulenes
  32996. oxaazabic
  32997. oxabicyclic
  32998. oxabicyclic
  32999. opening
  33000. oxabutadienes
  33001. oxacyclic
  33002. oxadiazepines
  33003. oxadiazetidines
  33004. oxadiazines
  33005. oxadiazocines
  33006. oxadiazoles
  33007. oxadiazolidines
  33008. oxadiazoline
  33009. oxadiazolines
  33010. oxadiazolopyrazines
  33011. oxadiazolopyridazine
  33012. oxadiazolopyridines
  33013. oxadiazolopyrimidine
  33014. oxadithiazetidines
  33015. oxadithiazines
  33016. oxadithietanes
  33017. oxadithiolanes
  33018. oxallyl
  33019. oxametallacycle
  33020. penams
  33021. oxaselenolanes
  33022. oxaselenolanes
  33023. thiaselenolanes
  33024. diselenolan
  33025. oxaselenoles
  33026. oxaselenoles
  33027. oxatellurolanes
  33028. oxatelluroles
  33029. oxathia
  33030. oxathiadiazepines
  33031. oxathiadiazines
  33032. oxathiane
  33033. oxathianes
  33034. oxathiazetidines
  33035. oxathiazines
  33036. oxathiazines
  33037. dioxazines
  33038. dithiazines
  33039. oxadiazines
  33040. thiadiazines
  33041. oxathietanes
  33042. oxathiins
  33043. oxathiolanes
  33044. oxatitana
  33045. oxatitanacyclopenten
  33046. oxatriazepines
  33047. oxatriazines
  33048. oxatriazoles
  33049. oxatriazolines
  33050. oxazaborolidine
  33051. oxazepines
  33052. oxazetidines
  33053. oxazin
  33054. oxazine
  33055. oxazines
  33056. oxazinone
  33057. oxazinones
  33058. oxazinones
  33059. thiazinones
  33060. oxaziridine
  33061. oxaziridine
  33062. oxidation
  33063. reagent
  33064. review
  33065. sulfone
  33066. phenylsulfonyl
  33067. oxaziridine
  33068. perfluoro
  33069. oxidation
  33070. silane
  33071. silanol
  33072. enantioselect
  33073. oxaziridines
  33074. oxaziridines
  33075. diaziridines
  33076. diaziridinones
  33077. diaziridinimines
  33078. oxazocines
  33079. oxazole
  33080. oxazole
  33081. oxazole
  33082. metalation
  33083. oxazoles
  33084. oxazolidine
  33085. oxazolidinediones
  33086. oxazolidines
  33087. oxazolidinone
  33088. oxazolines
  33089. oxazolines
  33090. delta
  33091. thiazolines
  33092. delta
  33093. oxazolines
  33094. amides
  33095. oxazolines
  33096. utility
  33097. acids
  33098. oxazolinone
  33099. oxazolomycin
  33100. oxazolones
  33101. oxazolooxazoles
  33102. oxazolopyrazines
  33103. oxazolopyridazines
  33104. oxazolopyridines
  33105. oxazolopyrimidines
  33106. oxenium
  33107. oxenium
  33108. cyclization
  33109. oxepane
  33110. oxepane
  33111. synthesis
  33112. oxepene
  33113. oxepines
  33114. oxetane
  33115. oxetane
  33116. opening
  33117. oxetane
  33118. opening
  33119. thiophenyl
  33120. carbanion
  33121. lithiate
  33122. oxetane
  33123. synthesis
  33124. oxetanes
  33125. oxetanocin
  33126. oxetanones
  33127. ation
  33128. oxidant
  33129. oxidati
  33130. oxidation
  33131. oxidation
  33132. oxidation
  33133. ation
  33134. elimination
  33135. oxidation
  33136. alkenes
  33137. oxidation
  33138. furan
  33139. oxidation
  33140. enolate
  33141. hydroxy-ketone
  33142. oxidation
  33143. enolate
  33144. oxaziridine
  33145. oxidation
  33146. oxazole
  33147. preparation
  33148. thiazole
  33149. amino
  33150. amine
  33151. ester
  33152. oxidation
  33153. review
  33154. chiral
  33155. oxaziridine
  33156. sulfonyl
  33157. induction
  33158. asymm
  33159. oxidation
  33160. selective
  33161. reagent
  33162. preparation
  33163. review
  33164. manganese
  33165. oxidations
  33166. oxidative
  33167. oxidative
  33168. addition
  33169. metallacycle
  33170. annelation
  33171. reaction
  33172. oxidative
  33173. coupling
  33174. oxidative
  33175. cyclization
  33176. oxide
  33177. oxide
  33178. oxidizing
  33179. oxidosqualene
  33180. oxime
  33181. oxime
  33182. benzoate
  33183. tributylfin
  33184. hydride
  33185. iminyl
  33186. radical
  33187. alkene
  33188. oxime
  33189. conversion
  33190. hydrolysis
  33191. reagent
  33192. cleavage
  33193. catalytic
  33194. carbo
  33195. oxime
  33196. ethers
  33197. oxime
  33198. ethers
  33199. intramolecular
  33200. addition
  33201. stereo
  33202. selectivity
  33203. oxime
  33204. olefin
  33205. cycloaddition
  33206. additions
  33207. analogs
  33208. oximes
  33209. oxindole
  33210. oxindole
  33211. synthesis
  33212. oxirane
  33213. oxirane
  33214. opening
  33215. review
  33216. tandem
  33217. barton
  33218. alcohol
  33219. radical
  33220. oxiranes
  33221. oxiranes
  33222. allyl
  33223. anion
  33224. delta
  33225. lactones
  33226. asymmetric
  33227. synthesis
  33228. oxirene
  33229. oxoalkanamides
  33230. oxoalkanedioic
  33231. oxoalkanoates
  33232. oxoalkylation
  33233. oxoalkylation
  33234. oxocanes
  33235. oxocanones
  33236. oxocene
  33237. oxocene
  33238. synthesis
  33239. oxocin
  33240. oxocins
  33241. oxoester
  33242. oxolactone
  33243. oxone
  33244. oxone
  33245. oxidation
  33246. oxonins
  33247. oxonins
  33248. azonines
  33249. thionins
  33250. phosphonins
  33251. azaannulenes
  33252. thiaannul
  33253. oxonium
  33254. oxonium
  33255. oxonium
  33256. cyclization
  33257. oxotitanium
  33258. oxotitanium
  33259. species
  33260. allyl
  33261. cation
  33262. review
  33263. cycloaddition
  33264. rearrangement
  33265. controlled
  33266. nucleophilic
  33267. additions
  33268. mercuration
  33269. oxy-anion
  33270. oxy-anion
  33271. electrocyclic
  33272. opening
  33273. oxy-cope
  33274. oxy-palladation
  33275. oxyallyl
  33276. oxyamination
  33277. oxycarbene
  33278. oxycarbenes
  33279. oxygenD
  33280. oxygen
  33281. transfer
  33282. carbonyl
  33283. oxides
  33284. shift
  33285. ozone
  33286. oxygenase
  33287. oxygenationD
  33288. oxymercuration
  33289. oxypalladation
  33290. oxyphosphonium
  33291. oxyphosphorane
  33292. ozone
  33293. ozonide
  33294. ozonides
  33295. ozonization
  33296. ozonolysis
  33297. simpkins
  33298. lithium
  33299. amide
  33300. chiral
  33301. amine
  33302. enolate
  33303. p'-di-tert-butylphen
  33304. p'-di-tert-butylphen
  33305. p-allyl
  33306. species
  33307. p-allyl
  33308. complex
  33309. p-allyl
  33310. intermediate
  33311. p-methoxybenzyl
  33312. p-methoxybenzyl
  33313. ester
  33314. p-methoxyphenyl
  33315. p-nitrobenzyl
  33316. p-nitrobenzyl
  33317. ester
  33318. p-quinones
  33319. padwa
  33320. padwa
  33321. carbene
  33322. rhodium
  33323. diazo
  33324. carbonyl
  33325. cyclopropane
  33326. vinyl
  33327. padwa
  33328. vinyl
  33329. sulfone
  33330. allene
  33331. review
  33332. cyclization
  33333. cycloaddition
  33334. silane
  33335. review
  33336. silicon
  33337. carbonyl
  33338. pairs
  33339. palladacycle
  33340. palladium
  33341. palladium
  33342. palladium
  33343. asymmetric
  33344. silylation
  33345. palladium
  33346. carbonylation
  33347. palladium
  33348. carbonylation
  33349. reaction
  33350. palladium
  33351. catalysis
  33352. alkynyl
  33353. carbonate
  33354. alkynyl
  33355. formate
  33356. palladium
  33357. catalysis
  33358. allylic
  33359. alkylation
  33360. axial
  33361. chirality
  33362. enant
  33363. palladium
  33364. catalysis
  33365. aromatic
  33366. halide
  33367. amine
  33368. amination
  33369. palladium
  33370. catalysis
  33371. domino
  33372. coupling
  33373. processes
  33374. palladium
  33375. catalyst
  33376. catalyst
  33377. mediated
  33378. alkylation
  33379. palladium
  33380. catalyzed
  33381. alkylation
  33382. palladium
  33383. catalyzed
  33384. annulation
  33385. palladium
  33386. catalyzed
  33387. carbonylation
  33388. palladium
  33389. catalyzed
  33390. coulping
  33391. palladium
  33392. catalyzed
  33393. coupling
  33394. palladium
  33395. catalyzed
  33396. coupling
  33397. bornic
  33398. acids
  33399. palladium
  33400. catalyzed
  33401. coupling
  33402. reaction
  33403. palladium
  33404. catalyzed
  33405. cyclization
  33406. palladium
  33407. catalyzed
  33408. hydrostannation
  33409. palladium
  33410. catalyzed
  33411. hydrostannylation
  33412. palladium
  33413. catalyzed
  33414. intramolecular
  33415. cyclization
  33416. palladium
  33417. catalyzed
  33418. lactonization
  33419. palladium
  33420. catalyzed
  33421. polycyclization
  33422. anion
  33423. capture
  33424. processes
  33425. palladium
  33426. catalyzed
  33427. reaction
  33428. formation
  33429. arylboronic
  33430. palladium
  33431. catalyzed
  33432. reactions
  33433. allylpalladium
  33434. complexes
  33435. palladium
  33436. catalyzed
  33437. expansion
  33438. palladium
  33439. catalyzed
  33440. stille
  33441. coupling
  33442. palladium
  33443. catalyzed
  33444. vinylation
  33445. palladium
  33446. catalyzed
  33447. vinylation
  33448. acetylene
  33449. derivatives
  33450. organic
  33451. palladium
  33452. catalyzed
  33453. vinylation
  33454. phase
  33455. transfer
  33456. conditions
  33457. palladium
  33458. catalzed
  33459. coupling
  33460. palladium
  33461. cephalosporin
  33462. allene
  33463. cuprate
  33464. stannane
  33465. cross
  33466. coupli
  33467. palladium
  33468. chemistry
  33469. palladium
  33470. cobalt
  33471. alkyl
  33472. crystal
  33473. structure
  33474. oxygen
  33475. ligand
  33476. tripo
  33477. palladium
  33478. complex
  33479. palladium
  33480. cyclization
  33481. reaction
  33482. palladium
  33483. hydrostannylation
  33484. palladium
  33485. catalyst
  33486. palladium
  33487. intramolecular
  33488. arylation
  33489. ethers
  33490. hexah
  33491. palladium
  33492. intermediates
  33493. palladium
  33494. mediated
  33495. cyclization
  33496. palladium
  33497. nickel
  33498. palladium
  33499. polyene
  33500. cyclization
  33501. furans
  33502. halenaquinone
  33503. xestoquin
  33504. palladium
  33505. stille
  33506. coupling
  33507. palladium
  33508. suzuki
  33509. coupling
  33510. palladium
  33511. synthesis
  33512. review
  33513. bifunctional
  33514. reagent
  33515. piers
  33516. palladium-catalysed
  33517. pandey
  33518. pandey
  33519. review
  33520. amine
  33521. photochem
  33522. electron
  33523. transfer
  33524. iminium
  33525. paniculatine
  33526. papulacandin
  33527. paquette
  33528. paquette
  33529. cyclooctatetraene
  33530. inversion
  33531. review
  33532. racemizatio
  33533. paquette
  33534. substitution
  33535. allylic
  33536. cyclopropane
  33537. cyclobutane
  33538. paraformaldehyde
  33539. parallel
  33540. paramagnetic
  33541. parameter
  33542. parameters
  33543. parinaric
  33544. parker
  33545. parkinsons
  33546. parnes
  33547. parnes
  33548. silicon
  33549. lewis
  33550. allyl
  33551. silyl
  33552. review
  33553. desilylation
  33554. parnes
  33555. synthesis
  33556. silicon
  33557. desilylation
  33558. equivalent
  33559. lewis
  33560. participation
  33561. pasto
  33562. pasto
  33563. allene
  33564. review
  33565. dipolar
  33566. cycloaddition
  33567. review
  33568. writing
  33569. pasto
  33570. allene
  33571. synthesis
  33572. cycloaddition
  33573. alkene
  33574. review
  33575. photochem
  33576. paterno
  33577. paterno
  33578. buchi
  33579. reaction
  33580. paterno
  33581. buchi
  33582. reaction
  33583. photochemical
  33584. reactions
  33585. paterson
  33586. paterson
  33587. epoxide
  33588. chiral
  33589. lewis
  33590. nucleophilic
  33591. opening
  33592. paths
  33593. pathways
  33594. paton
  33595. patterns
  33596. patterson
  33597. patwardhan
  33598. patwardhan
  33599. paulownin
  33600. pausand
  33601. pausand
  33602. khand
  33603. cyclization
  33604. pauson
  33605. pauson
  33606. khand
  33607. pauson
  33608. khand
  33609. alkyne
  33610. cyclopentenone
  33611. organometallic
  33612. cobalt
  33613. pauson
  33614. khand
  33615. reaction
  33616. pauson
  33617. khand
  33618. reaction
  33619. intramolecular
  33620. methylenecyclopropan
  33621. payneE
  33622. allylic
  33623. oxidation
  33624. catalyzed
  33625. arylation
  33626. pearson
  33627. reduction
  33628. azide
  33629. amine
  33630. hydride
  33631. reducing
  33632. agent
  33633. isoxazole
  33634. pelter
  33635. pelter
  33636. intramolecular
  33637. diels
  33638. alder
  33639. cycloaddition
  33640. furan
  33641. hetero
  33642. pendant
  33643. penem
  33644. penicillin
  33645. penicillin
  33646. ketones
  33647. pentaammineosmium
  33648. pentacarbonyl
  33649. pentacyclic
  33650. pentacyclic
  33651. triterpenes
  33652. arborane
  33653. pentadienylborane
  33654. pentafluorophenyl
  33655. pentane
  33656. pentanone
  33657. pentathiepin
  33658. pentazines
  33659. pentenylamines
  33660. peptide
  33661. peptide
  33662. coupling
  33663. peptide
  33664. cyclizations
  33665. solid
  33666. chemistry
  33667. polymer
  33668. peptide
  33669. synthesis
  33670. peptides
  33671. peptides
  33672. proteins
  33673. enzymes
  33674. peptidyl
  33675. peracid
  33676. perchlo
  33677. perchlorate
  33678. trimethyl
  33679. trichloro
  33680. buten
  33681. perchlorovinylcarben
  33682. perfluoro
  33683. perfluorobutyrate
  33684. perfluorophenyl
  33685. perhydro
  33686. perhydrohistrionicot
  33687. selenium
  33688. participation
  33689. molecular
  33690. oxygen
  33691. anodic
  33692. oxidatio
  33693. pericyclic
  33694. pericyclic
  33695. pericyclic
  33696. sequenes
  33697. peridinin
  33698. peridinin
  33699. chromophore
  33700. perimeter
  33701. periodate
  33702. inane
  33703. periodinane
  33704. iodinane
  33705. peristylane
  33706. perkin
  33707. perlman
  33708. permanganate
  33709. peroxide
  33710. peroxides
  33711. peroxy
  33712. peroxyamines
  33713. peroxydicarbonates
  33714. peroxydisulfate
  33715. perrin
  33716. perrin
  33717. review
  33718. amide
  33719. mechanism
  33720. chemistry
  33721. exchange
  33722. proton
  33723. perruthenate
  33724. persulfate
  33725. perturbation
  33726. peters
  33727. peters
  33728. lanthanide
  33729. shift
  33730. review
  33731. structure
  33732. determination
  33733. peterson
  33734. olefination
  33735. petragnani
  33736. petragnani
  33737. anion
  33738. dianion
  33739. ester
  33740. alkylation
  33741. experimental
  33742. petragnani
  33743. tellurium
  33744. radical
  33745. carbanion
  33746. review
  33747. petrzilka
  33748. petrzilka
  33749. dipolar
  33750. cycloaddition
  33751. cyclopentadiene
  33752. review
  33753. heter
  33754. pfaltz
  33755. pfaltz
  33756. review
  33757. catalyst
  33758. chiral
  33759. cyclopropane
  33760. cyclopropanation
  33761. pgf2a
  33762. sical
  33763. organic
  33764. energy
  33765. calculations
  33766. sical
  33767. organic
  33768. reactive
  33769. intermediates
  33770. strained
  33771. molecules
  33772. tochemistry
  33773. ph2nch
  33774. ph2nch2sph
  33775. ph2nch2tbu
  33776. ph3as
  33777. ph3as
  33778. ph3sb
  33779. ph3sb
  33780. phaeophyceae
  33781. pharmacophore
  33782. phase
  33783. phase
  33784. transfer
  33785. catalysis
  33786. coupling
  33787. reactions
  33788. organic
  33789. halides
  33790. phase
  33791. transfer
  33792. catalysis
  33793. organic
  33794. synthesis
  33795. improvement
  33796. phase
  33797. transfer
  33798. catalysis
  33799. oxidative
  33800. decyanation
  33801. phase
  33802. transfer
  33803. catalyst
  33804. review
  33805. experimental
  33806. phase
  33807. transfer
  33808. reagents
  33809. alcohols
  33810. phenanthrene
  33811. phenanthrenecarboxyl
  33812. phenanthrenes
  33813. phenanthridine
  33814. phenanthridines
  33815. phenanthrolines
  33816. phenaz
  33817. phenazi
  33818. phenazines
  33819. phenes
  33820. phenol
  33821. phenol
  33822. phenoxide
  33823. addition
  33824. anion
  33825. alkyne
  33826. baldwin
  33827. intramolecula
  33828. phenol
  33829. synthesis
  33830. phenol
  33831. thiophenyl
  33832. pummerer
  33833. rearrangement
  33834. sulfoxonium
  33835. phenolate
  33836. phenolic
  33837. phenolic
  33838. hydroxyl
  33839. tetraacetate
  33840. replacement
  33841. carbonyl
  33842. phenols
  33843. phenols
  33844. synthesis
  33845. phenothiazines
  33846. phenoxathiins
  33847. phenoxide
  33848. phenoxy
  33849. phenyl
  33850. phenyl
  33851. boronic
  33852. phenyl
  33853. selenation
  33854. phenyl
  33855. sulfones
  33856. phenylalkenyl
  33857. phenylcarbene
  33858. phenylchlorocarbene
  33859. phenylene
  33860. phenyleneethynylene
  33861. phenylethyl
  33862. phenylglycinol
  33863. phenylglycinol
  33864. derived
  33865. lactam
  33866. lithium
  33867. enolate
  33868. alkylation
  33869. phenyliodine
  33870. phenyliodine
  33871. diacetate
  33872. radical
  33873. oxidation
  33874. phenylpyrazolidin
  33875. phenylsulfonyl
  33876. phenylsulfonyl
  33877. acetonitrile
  33878. phenylsulfonylhydraz
  33879. phenylsulfonyloxazir
  33880. phenylthio
  33881. phenylthio
  33882. migration
  33883. asymmetric
  33884. synthesis
  33885. chiral
  33886. centers
  33887. phenylthio
  33888. migration
  33889. asymmetric
  33890. synthesis
  33891. enantioselective
  33892. phenylthiocyclobutyl
  33893. phenyltriflimide
  33894. phenyltrimethylammon
  33895. pheromone
  33896. pheromones
  33897. philosophy
  33898. phntf2
  33899. phophine
  33900. phophine-borane
  33901. phorbol
  33902. phosgene
  33903. phosphacumulene
  33904. phosphane
  33905. phosphane
  33906. oxide
  33907. phosphate
  33908. phosphates
  33909. phosphazenes
  33910. phospherane
  33911. phosphine
  33912. phosphine
  33913. hydroformylation
  33914. phosphine
  33915. ligand
  33916. phosphines
  33917. phosphinyl
  33918. phosphite
  33919. phosphites
  33920. phospholanes
  33921. phospholenes
  33922. phospholes
  33923. phosphonate
  33924. phosphonate
  33925. stereoselective
  33926. synthesis
  33927. cuprate
  33928. addition
  33929. phosp
  33930. phosphonates
  33931. phosphonates
  33932. phosphorus
  33933. analogs
  33934. phosphonic
  33935. ylphosphorany
  33936. phosphorane
  33937. phosphoranes
  33938. phosphorinanes
  33939. phosphorinanes
  33940. phosphorins
  33941. phospholanes
  33942. phospholenes
  33943. phospho
  33944. phosphorins
  33945. phosphorous
  33946. phosphorous
  33947. review
  33948. wittig
  33949. reagent
  33950. conditions
  33951. experimental
  33952. phosphorus
  33953. phosphorus
  33954. compounds
  33955. phosphorus
  33956. reagent
  33957. banion
  33958. phosphorus
  33959. ylide
  33960. condensation
  33961. photo
  33962. photo
  33963. induced
  33964. electron
  33965. transfer
  33966. photo-fries
  33967. photoacoustic
  33968. photoaddition
  33969. photoadducts
  33970. photoannulation
  33971. photoc
  33972. photochem
  33973. photochemi
  33974. photochemical
  33975. ulation
  33976. photochemical
  33977. annulation
  33978. photochemical
  33979. cleavage
  33980. amino
  33981. ketone
  33982. asymmetric
  33983. photochemical
  33984. formation
  33985. annulations
  33986. photochemistry
  33987. photochemical
  33988. formation
  33989. aromatics
  33990. functionalis
  33991. photochemical
  33992. formation
  33993. pericyclic
  33994. reactions
  33995. cycloa
  33996. photochemical
  33997. chromium
  33998. carbene
  33999. complex
  34000. stereochem
  34001. torquosele
  34002. photochemical
  34003. electron
  34004. transfer
  34005. photochemistry
  34006. photochemical
  34007. oxaziridine
  34008. rearrangement
  34009. photochemical
  34010. photochemi
  34011. photochemical
  34012. photochemical
  34013. photochemistry
  34014. thioketones
  34015. photochemical
  34016. photochemical
  34017. reactivity
  34018. photogenerated
  34019. reagents
  34020. cyclod
  34021. photochemical
  34022. photochemical
  34023. transformations
  34024. thiocarbonyl
  34025. ylides
  34026. methylid
  34027. photochemistry
  34028. photochemical
  34029. annulation@
  34030. photochemical
  34031. schmidt@
  34032. photochemistry
  34033. photochemistry
  34034. electrocyclic
  34035. closure
  34036. shift
  34037. sulfur
  34038. nisms
  34039. intramolecular@
  34040. physical
  34041. organic
  34042. mechanisms
  34043. substitution
  34044. electrophilic
  34045. aroma@
  34046. physical
  34047. organic
  34048. reactive
  34049. intermediates
  34050. carbenoids
  34051. carbenes@
  34052. physical
  34053. organic
  34054. reactive
  34055. intermediates
  34056. miscellaneous
  34057. hetary@
  34058. physical
  34059. organic
  34060. reactive
  34061. intermediates
  34062. radicals
  34063. physical
  34064. organic
  34065. reactive
  34066. intermediates
  34067. strained
  34068. molecules
  34069. physical
  34070. organic
  34071. rearrangements
  34072. photoc
  34073. emical
  34074. reactions
  34075. physical
  34076. organic
  34077. stereochemistry
  34078. carbring
  34079. cyclooctane@
  34080. physical
  34081. organic
  34082. stereochemistry
  34083. stereoelectronics
  34084. organomet@
  34085. pi-facial
  34086. selectivity/chiral
  34087. alkoxy
  34088. dienes/carbohydrate
  34089. temp@
  34090. pinto
  34091. anomeric
  34092. writing
  34093. effect
  34094. sulfur
  34095. reference
  34096. review
  34097. confor@
  34098. polarization
  34099. transfer
  34100. enhancement
  34101. selective
  34102. population
  34103. inver@
  34104. poly@
  34105. porphyrin
  34106. complexes
  34107. hydrosilylation
  34108. ketones
  34109. olefins@
  34110. photochemistry
  34111. sulfur
  34112. photochemistry
  34113. reactive
  34114. intermediates
  34115. biradicals
  34116. photochemistry
  34117. stereoselective
  34118. bromination
  34119. deoxygenation
  34120. photoconversion
  34121. photocyclisation
  34122. photocyclization
  34123. photocycloaddition
  34124. photodehydrocyclizat
  34125. photoelectron
  34126. photogenerated
  34127. photoinduced
  34128. photoinduced
  34129. electron
  34130. transfer
  34131. photolysis
  34132. photooxidation
  34133. photooxygenation
  34134. photophysical
  34135. photoreactions
  34136. photorearrangement
  34137. photosensitization
  34138. photosensitized
  34139. photosynthesis
  34140. photoxidation
  34141. phthalazines
  34142. phthalide
  34143. phthalimides
  34144. phthalimidesulfenyl
  34145. phthalimidesulfenyl
  34146. chloride
  34147. addition
  34148. arylalkynes
  34149. benzo
  34150. phthalimidosulfenyl
  34151. organic
  34152. stereoelectronics
  34153. mechanisms
  34154. kinetically-co
  34155. organic
  34156. mechanisms
  34157. stereoelectronics
  34158. organic
  34159. reactive
  34160. intermediates
  34161. carbenoids
  34162. ylide
  34163. physi
  34164. physi
  34165. organic
  34166. stereoelectronics
  34167. stereochemistry
  34168. ketones
  34169. physic
  34170. physic
  34171. organic
  34172. rearrangements
  34173. physica
  34174. physica
  34175. organic
  34176. stereochemistry
  34177. mechanisms
  34178. olefins
  34179. acetylene
  34180. physical
  34181. physical
  34182. physical
  34183. physical
  34184. reactive
  34185. intermediates
  34186. radicals
  34187. homolysis
  34188. physical
  34189. reactive
  34190. intermediates
  34191. radicals
  34192. physical
  34193. organ
  34194. rearrangements
  34195. physical
  34196. organi
  34197. reactive
  34198. intermediates
  34199. carbenoids
  34200. physical
  34201. organic
  34202. physical
  34203. organic
  34204. formation
  34205. aromatics
  34206. chain
  34207. appendag
  34208. physical
  34209. organic
  34210. formation
  34211. aromatics
  34212. functiona
  34213. physical
  34214. organic
  34215. formation
  34216. pericyclic
  34217. reactions
  34218. physical
  34219. organic
  34220. computer
  34221. cyclization
  34222. bimolecular
  34223. addition
  34224. physical
  34225. organic
  34226. contrapolarization
  34227. physical
  34228. organic
  34229. elimination
  34230. physical
  34231. organic
  34232. hanisms
  34233. annulation
  34234. intramolecular
  34235. physical
  34236. organic
  34237. anisms
  34238. physical
  34239. organic
  34240. mechan
  34241. alkenes
  34242. alkynes
  34243. acetylenes
  34244. physical
  34245. organic
  34246. mechanism
  34247. physical
  34248. organic
  34249. mechanisms
  34250. physical
  34251. organic
  34252. mechanisms
  34253. physical
  34254. organic
  34255. mechanisms
  34256. acids
  34257. deprotonation
  34258. proton
  34259. trans
  34260. physical
  34261. organic
  34262. mechanisms
  34263. arenes
  34264. aromatic
  34265. substitution
  34266. physical
  34267. organic
  34268. mechanisms
  34269. alkenes
  34270. nucleophilic
  34271. additio
  34272. physical
  34273. organic
  34274. mechanisms
  34275. alkenes
  34276. ozonolysis
  34277. physical
  34278. organic
  34279. mechanisms
  34280. deprotonation
  34281. proton
  34282. transfer
  34283. physical
  34284. organic
  34285. mechanisms
  34286. electron
  34287. transfer
  34288. physical
  34289. organic
  34290. mechanisms
  34291. electron-transfer
  34292. physical
  34293. organic
  34294. mechanisms
  34295. electrophilic
  34296. addition
  34297. alken
  34298. physical
  34299. organic
  34300. mechanisms
  34301. electrophilic
  34302. aromatic
  34303. substitut
  34304. physical
  34305. organic
  34306. mechanisms
  34307. electrophilic
  34308. substitution
  34309. oxida
  34310. physical
  34311. organic
  34312. mechanisms
  34313. elimination
  34314. physical
  34315. organic
  34316. mechanisms
  34317. elimination
  34318. physical
  34319. organic
  34320. mechanisms
  34321. elimination
  34322. alkenes
  34323. physical
  34324. organic
  34325. mechanisms
  34326. elimination
  34327. physical
  34328. organic
  34329. mechanisms
  34330. hydride
  34331. transfer
  34332. physical
  34333. organic
  34334. mechanisms
  34335. intramolecular
  34336. physical
  34337. organic
  34338. mechanisms
  34339. nitrosation
  34340. physical
  34341. organic
  34342. mechanisms
  34343. nucleophilic
  34344. substitution
  34345. physical
  34346. organic
  34347. mechanisms
  34348. nucleophilic
  34349. vinylic
  34350. substitutio
  34351. physical
  34352. organic
  34353. mechanisms
  34354. organometallics
  34355. physical
  34356. organic
  34357. mechanisms
  34358. organometallics
  34359. electron
  34360. physical
  34361. organic
  34362. mechanisms
  34363. physical
  34364. organic
  34365. mechanisms
  34366. radical
  34367. anion
  34368. subsitution
  34369. physical
  34370. organic
  34371. mechanisms
  34372. reacti
  34373. intermediates
  34374. radicals
  34375. physical
  34376. organic
  34377. mechanisms
  34378. rearrangements
  34379. physical
  34380. organic
  34381. mechanisms
  34382. rearrangements
  34383. carbonium
  34384. physical
  34385. organic
  34386. mechanisms
  34387. stereochemistry
  34388. elimination
  34389. physical
  34390. organic
  34391. mechanisms
  34392. stereochemistry
  34393. elimination
  34394. physical
  34395. organic
  34396. mechanisms
  34397. stereochemistry
  34398. functional
  34399. group
  34400. physical
  34401. organic
  34402. mechanisms
  34403. stereochemistry
  34404. heterolytic
  34405. physical
  34406. organic
  34407. mechanisms
  34408. stereochemistry
  34409. regiochemistry
  34410. physical
  34411. organic
  34412. mechanisms
  34413. substitution
  34414. electrophilic
  34415. aroma
  34416. physical
  34417. organic
  34418. mechanisms
  34419. substitution
  34420. nucleophilic
  34421. physical
  34422. organic
  34423. mechanisms
  34424. substitution
  34425. nucleophilic
  34426. elimin
  34427. physical
  34428. organic
  34429. organometallics
  34430. mechanisms
  34431. physical
  34432. organic
  34433. photochemical
  34434. reactions
  34435. photochemistry
  34436. physical
  34437. organic
  34438. reacti
  34439. intermediates
  34440. physical
  34441. organic
  34442. reactive
  34443. ermediates
  34444. miscellaneous
  34445. hetery
  34446. physical
  34447. organic
  34448. reactive
  34449. rmediates
  34450. strained
  34451. molecules
  34452. physical
  34453. organic
  34454. reactive
  34455. inter
  34456. ediates
  34457. radicals
  34458. physical
  34459. organic
  34460. reactive
  34461. intermediates
  34462. alkenes
  34463. aklynes
  34464. physical
  34465. organic
  34466. reactive
  34467. intermediates
  34468. alkenes
  34469. radical
  34470. physical
  34471. organic
  34472. reactive
  34473. intermediates
  34474. carbanions
  34475. physical
  34476. organic
  34477. reactive
  34478. intermediates
  34479. carbanions
  34480. stereoele
  34481. physical
  34482. organic
  34483. reactive
  34484. intermediates
  34485. carbanions
  34486. synthons
  34487. physical
  34488. organic
  34489. reactive
  34490. intermediates
  34491. carbenoids
  34492. carbanion
  34493. physical
  34494. organic
  34495. reactive
  34496. intermediates
  34497. carbenoids
  34498. carbenes
  34499. physical
  34500. organic
  34501. reactive
  34502. intermediates
  34503. carbenoids
  34504. carbenes
  34505. physical
  34506. organic
  34507. reactive
  34508. intermediates
  34509. carbenoids
  34510. metal
  34511. physical
  34512. organic
  34513. reactive
  34514. intermediates
  34515. carbenoids
  34516. rhodium
  34517. physical
  34518. organic
  34519. reactive
  34520. intermediates
  34521. carbenoids
  34522. stereoche
  34523. physical
  34524. organic
  34525. reactive
  34526. intermediates
  34527. carbonium
  34528. physical
  34529. organic
  34530. reactive
  34531. intermediates
  34532. carbonium
  34533. alken
  34534. physical
  34535. organic
  34536. reactive
  34537. intermediates
  34538. carbonium
  34539. carbo
  34540. physical
  34541. organic
  34542. reactive
  34543. intermediates
  34544. enols
  34545. physical
  34546. organic
  34547. reactive
  34548. intermediates
  34549. radicals
  34550. carbene
  34551. physical
  34552. organic
  34553. reactive
  34554. intermediates
  34555. mechanisms
  34556. radical
  34557. physical
  34558. organic
  34559. reactive
  34560. intermediates
  34561. miscellaneous
  34562. physical
  34563. organic
  34564. reactive
  34565. intermediates
  34566. miscellaneous
  34567. cycloa
  34568. physical
  34569. organic
  34570. reactive
  34571. intermediates
  34572. miscellaneous
  34573. hetary
  34574. physical
  34575. organic
  34576. reactive
  34577. intermediates
  34578. miscellaneous
  34579. nitren
  34580. physical
  34581. organic
  34582. reactive
  34583. intermediates
  34584. miscellaneous
  34585. ylids
  34586. physical
  34587. organic
  34588. reactive
  34589. intermediates
  34590. nitrenes
  34591. physical
  34592. organic
  34593. reactive
  34594. intermediates
  34595. radical
  34596. anion
  34597. physical
  34598. organic
  34599. reactive
  34600. intermediates
  34601. radical
  34602. cations
  34603. physical
  34604. organic
  34605. reactive
  34606. intermediates
  34607. radical
  34608. physical
  34609. organic
  34610. reactive
  34611. intermediates
  34612. radical
  34613. carbeno
  34614. physical
  34615. organic
  34616. reactive
  34617. intermediates
  34618. radical
  34619. ion-rad
  34620. physical
  34621. organic
  34622. reactive
  34623. intermediates
  34624. radical
  34625. mechani
  34626. physical
  34627. organic
  34628. reactive
  34629. intermediates
  34630. radicals
  34631. physical
  34632. organic
  34633. reactive
  34634. intermediates
  34635. radicals
  34636. alkenes
  34637. physical
  34638. organic
  34639. reactive
  34640. intermediates
  34641. radicals
  34642. arenes
  34643. physical
  34644. organic
  34645. reactive
  34646. intermediates
  34647. radicals
  34648. physical
  34649. organic
  34650. reactive
  34651. intermediates
  34652. radicals
  34653. physical
  34654. organic
  34655. reactive
  34656. intermediates
  34657. radicals
  34658. physical
  34659. organic
  34660. reactive
  34661. intermediates
  34662. radicals
  34663. physical
  34664. organic
  34665. reactive
  34666. intermediates
  34667. radicals
  34668. mechanisms
  34669. physical
  34670. organic
  34671. reactive
  34672. intermediates
  34673. radicals
  34674. photochemic
  34675. physical
  34676. organic
  34677. reactive
  34678. intermediates
  34679. radicals
  34680. radical
  34681. physical
  34682. organic
  34683. reactive
  34684. intermediates
  34685. radicals
  34686. stereochemi
  34687. physical
  34688. organic
  34689. reactive
  34690. intermediates
  34691. radicals
  34692. physical
  34693. organic
  34694. reactive
  34695. intermediates
  34696. ained
  34697. molecules
  34698. physical
  34699. organic
  34700. reactive
  34701. intermediates
  34702. strained
  34703. molecules
  34704. physical
  34705. organic
  34706. reactive
  34707. intermediates
  34708. strained
  34709. molecules
  34710. physical
  34711. organic
  34712. reactive
  34713. intermediates
  34714. strained
  34715. molecules
  34716. physical
  34717. organic
  34718. reactive
  34719. intermediates
  34720. strained
  34721. molecules
  34722. physical
  34723. organic
  34724. reactive
  34725. intermediates
  34726. strained
  34727. molecules
  34728. physical
  34729. organic
  34730. reactive
  34731. intermediates
  34732. strained
  34733. molecules
  34734. physical
  34735. organic
  34736. reactive
  34737. intermediates
  34738. strained
  34739. molecules
  34740. physical
  34741. organic
  34742. reactive
  34743. intermediates
  34744. strained
  34745. molecules
  34746. physical
  34747. organic
  34748. reactive
  34749. intermediates
  34750. ylides
  34751. physical
  34752. organic
  34753. reactive
  34754. intermediates
  34755. ylides
  34756. physical
  34757. organic
  34758. reactive
  34759. intermediates
  34760. ylides
  34761. physical
  34762. organic
  34763. reactive
  34764. ntermediates
  34765. radicals
  34766. physical
  34767. organic
  34768. rearrangements
  34769. physical
  34770. organic
  34771. rearrangements
  34772. alpha
  34773. diazocarbonyl
  34774. physical
  34775. organic
  34776. rearrangements
  34777. arenes
  34778. thermal
  34779. rearrangement
  34780. physical
  34781. organic
  34782. rearrangements
  34783. carbanions
  34784. physical
  34785. organic
  34786. rearrangements
  34787. carbenoids
  34788. nitrenes
  34789. carbenes
  34790. physical
  34791. organic
  34792. rearrangements
  34793. carbocations
  34794. physical
  34795. organic
  34796. rearrangements
  34797. homologation
  34798. physical
  34799. organic
  34800. rearrangements
  34801. pericyclic
  34802. physical
  34803. organic
  34804. rearrangements
  34805. photoc
  34806. emical
  34807. reactions
  34808. physical
  34809. organic
  34810. rearrangements
  34811. photochemical
  34812. physical
  34813. organic
  34814. rearrangements
  34815. photochemical
  34816. actions
  34817. physical
  34818. organic
  34819. rearrangements
  34820. photochemical
  34821. reactions
  34822. physical
  34823. organic
  34824. rearrangements
  34825. photochemical
  34826. reactions
  34827. physical
  34828. organic
  34829. rearrangements
  34830. photochemical
  34831. reactions
  34832. physical
  34833. organic
  34834. rearrangements
  34835. photochemical
  34836. reactions
  34837. physical
  34838. organic
  34839. rearrangements
  34840. reactive
  34841. intermediates
  34842. carba
  34843. physical
  34844. organic
  34845. rearrangements
  34846. reactive
  34847. intermediates
  34848. carbo
  34849. physical
  34850. organic
  34851. rearrangements
  34852. physical
  34853. organic
  34854. stereochemis
  34855. silicon
  34856. physical
  34857. organic
  34858. stereochemistry
  34859. physical
  34860. organic
  34861. stereochemistry
  34862. carbocations
  34863. carboanions
  34864. physical
  34865. organic
  34866. stereochemistry
  34867. carbring
  34868. physical
  34869. organic
  34870. stereochemistry
  34871. carbring
  34872. physical
  34873. organic
  34874. stereochemistry
  34875. carbring
  34876. cyclooctane
  34877. physical
  34878. organic
  34879. stereochemistry
  34880. conformation
  34881. physical
  34882. organic
  34883. stereochemistry
  34884. conformation
  34885. rbring
  34886. physical
  34887. organic
  34888. stereochemistry
  34889. conformation
  34890. heterocycles
  34891. physical
  34892. organic
  34893. stereochemistry
  34894. conformation
  34895. hydroxylamines
  34896. physical
  34897. organic
  34898. stereochemistry
  34899. conformation
  34900. physical
  34901. organic
  34902. stereochemistry
  34903. conformational
  34904. analysis
  34905. physical
  34906. organic
  34907. stereochemistry
  34908. conformational
  34909. analysis
  34910. physical
  34911. organic
  34912. stereochemistry
  34913. conformational
  34914. analysis
  34915. physical
  34916. organic
  34917. stereochemistry
  34918. enols
  34919. enolates
  34920. protonation
  34921. physical
  34922. organic
  34923. stereochemistry
  34924. heterocycles
  34925. physical
  34926. organic
  34927. stereochemistry
  34928. kinetic
  34929. resolution
  34930. physical
  34931. organic
  34932. stereochemistry
  34933. physical
  34934. organic
  34935. stereochemistry
  34936. organometallics
  34937. general
  34938. physical
  34939. organic
  34940. stereochemistry
  34941. physical
  34942. organic
  34943. stereochemistry
  34944. stereoelectronics
  34945. physical
  34946. organic
  34947. stereochemistry
  34948. stereoelectronics
  34949. organomet
  34950. physical
  34951. organic
  34952. stereoelectronics
  34953. physical
  34954. organic
  34955. stereoelectronics
  34956. addition
  34957. physical
  34958. organic
  34959. stereoelectronics
  34960. acetals
  34961. hydroly
  34962. physical
  34963. organic
  34964. stereoelectronics
  34965. carbonium
  34966. silicon
  34967. physical
  34968. organic
  34969. stereoelectronics
  34970. physical
  34971. organic
  34972. stereoelectronics
  34973. stereochemistry
  34974. physical
  34975. organic
  34976. stereoelectronics
  34977. stereochemistry
  34978. conformat
  34979. physical
  34980. organic
  34981. physical
  34982. organic
  34983. rearrangement
  34984. physical
  34985. rganic
  34986. reactive
  34987. intermediates
  34988. carbonium
  34989. strain
  34990. physicochemical
  34991. phytotoxic
  34992. allyl
  34993. palladium
  34994. faces
  34995. carbonyl
  34996. groups
  34997. olefin
  34998. groups
  34999. interactions
  35000. facial
  35001. diastereoselection
  35002. lewis
  35003. allylic
  35004. substituents
  35005. methane
  35006. rearrangement
  35007. gamma
  35008. butyrolactone
  35009. hydroxy
  35010. esters
  35011. pi-facial
  35012. pi-facial
  35013. selectivity/chiral
  35014. alkoxy
  35015. dienes/carbohydrate
  35016. piancatelli
  35017. piancatelli
  35018. course
  35019. furan
  35020. heterocycle
  35021. review
  35022. hydrolysis
  35023. piclavines
  35024. pictet
  35025. pictet
  35026. spengler
  35027. pictet
  35028. spengler
  35029. condensation
  35030. pictet
  35031. spengler
  35032. cyclization
  35033. pictet
  35034. spengler
  35035. reaction
  35036. pictet
  35037. spengler
  35038. reaction
  35039. alkaloids
  35040. pictet
  35041. spengler
  35042. reaction
  35043. tetrahydro
  35044. carbolines
  35045. pictet-spengler
  35046. pictet-spengler
  35047. reaction
  35048. fusion
  35049. review
  35050. student
  35051. liver
  35052. esterase
  35053. dehydrogenase
  35054. catalyzed
  35055. oxidations
  35056. lewis
  35057. pigment
  35058. pillared
  35059. pimarolide
  35060. pimarolide
  35061. methyl
  35062. ester
  35063. pinacol
  35064. pinacol
  35065. coupling
  35066. alkene
  35067. carbonyl
  35068. titanium
  35069. metal
  35070. reagent
  35071. pinacol
  35072. rearrangement
  35073. pinder
  35074. pinder
  35075. review
  35076. synthesis
  35077. reduction
  35078. halide
  35079. hydrogenation
  35080. exper
  35081. pinene
  35082. pinhey
  35083. pinto
  35084. pinto
  35085. anomeric
  35086. writing
  35087. effect
  35088. sulfur
  35089. reference
  35090. review
  35091. confor
  35092. pipecolic
  35093. pipecolic
  35094. piperideines
  35095. piperidine
  35096. piperidine
  35097. pyrrolidine
  35098. indolizidine
  35099. amino
  35100. alcohol
  35101. cyclizatio
  35102. piperidines
  35103. piperidines
  35104. piperideines
  35105. dihydropyridines
  35106. pirkle
  35107. pivalate
  35108. planar
  35109. plane
  35110. plane
  35111. nonsymmetric
  35112. cyclopentadienes
  35113. alder
  35114. plant
  35115. plants
  35116. platelet
  35117. platelets
  35118. platinum
  35119. platinum
  35120. catalyst
  35121. platz
  35122. platz
  35123. carbene
  35124. theory
  35125. review
  35126. writing
  35127. spectroscopy
  35128. cyclopropen
  35129. plesset
  35130. plesset
  35131. perturbation
  35132. theory
  35133. microsomal
  35134. cytochrome
  35135. plumboles
  35136. podocarpic
  35137. podocarpic
  35138. lithium
  35139. copper
  35140. benzannulation
  35141. radical
  35142. podraza
  35143. poison
  35144. polar
  35145. polarity
  35146. polarization
  35147. polarization
  35148. transfer
  35149. enhancement
  35150. selective
  35151. population
  35152. inver
  35153. pollack
  35154. pollard
  35155. polonovski
  35156. polonovski
  35157. rearrangement
  35158. polyamide
  35159. polyamides
  35160. polyazapentadienes
  35161. polycarbonate
  35162. polycyclic
  35163. polycyclic
  35164. biphenylenes
  35165. resonance
  35166. theory
  35167. phenylene
  35168. systems
  35169. polycyclization
  35170. polydetides
  35171. polyene
  35172. polyenes
  35173. polyether
  35174. polyether
  35175. antibiotics
  35176. stereocontrolled
  35177. synthesis
  35178. tetrahydrop
  35179. polyfunctional
  35180. polyhydroxylated
  35181. polyhydroxylated
  35182. natural
  35183. products
  35184. polym
  35185. polymer
  35186. polymer
  35187. supported
  35188. peptide
  35189. synthesis
  35190. polymerization
  35191. polymers
  35192. polypropionate
  35193. polysubstituted
  35194. polysulfides
  35195. polyynes
  35196. pommer
  35197. pommer
  35198. review
  35199. wittig
  35200. alkylation
  35201. phosphorous
  35202. industry
  35203. alkene
  35204. population
  35205. porphyrin
  35206. porphyrin
  35207. complexes
  35208. hydrosilylation
  35209. ketones
  35210. olefins
  35211. porphyrins
  35212. porter
  35213. porter
  35214. radical
  35215. cyclization
  35216. macro
  35217. large
  35218. review
  35219. positions
  35220. possibilities
  35221. postema
  35222. postema
  35223. carbohydrate
  35224. review
  35225. carbon
  35226. glycoside
  35227. wittig
  35228. palladiu
  35229. potassium
  35230. potassium
  35231. acetate
  35232. potassium
  35233. borohyride
  35234. potassium
  35235. butoxide
  35236. potassium
  35237. hydride
  35238. convenient
  35239. metalation
  35240. kaliation
  35241. reduction
  35242. potassium
  35243. hydride
  35244. rearrangements
  35245. potent
  35246. potent
  35247. antitumor
  35248. antibiotics
  35249. potent
  35250. antitumor
  35251. antibiotics
  35252. neocarzinostatin
  35253. chromophore
  35254. potent
  35255. antitumor
  35256. antibiotics
  35257. neocarzinostatin
  35258. chromophore
  35259. potential
  35260. potential
  35261. functions
  35262. simulations
  35263. potential
  35264. sialidase
  35265. inhibitors
  35266. alpha
  35267. glucosidase
  35268. inhibitors
  35269. potential
  35270. sialidase
  35271. inhibitors
  35272. alpha
  35273. glucosidase
  35274. inhibitors
  35275. powder
  35276. powerful
  35277. pph2cl
  35278. practical
  35279. precoccinelline
  35280. precoccinelline
  35281. myrrhine
  35282. corvergine
  35283. hippodamine
  35284. hippocasine
  35285. precursor
  35286. precursors
  35287. prenyl
  35288. prenyl
  35289. boronate
  35290. amine
  35291. b-unsaturated
  35292. lactone
  35293. a-alkoxyl
  35294. a-nitroso
  35295. iodides
  35296. a-glucosides
  35297. a-hydroxy
  35298. ketone
  35299. a-hydroxy
  35300. ester
  35301. a-trimethylsilyloxy
  35302. cyanide
  35303. alcohol
  35304. alkene
  35305. allylic
  35306. alcohol
  35307. allylic
  35308. stannane
  35309. silane
  35310. b-cyanoalkene
  35311. b-hydroxysulfoxide
  35312. potential
  35313. sialidase
  35314. inhibitors
  35315. alpha
  35316. glucosidase
  35317. inhibitors
  35318. carboxylic
  35319. acid@
  35320. preparations
  35321. probes@
  35322. ative
  35323. decarboxylation
  35324. iminium
  35325. mannich
  35326. proposed@
  35327. protection
  35328. proteins@
  35329. pyranoquinone@
  35330. pyrazoles
  35331. isoxazoles
  35332. isothiazoles
  35333. imidazoles
  35334. oxazoles
  35335. thiazo@
  35336. pyridine
  35337. heteroaromatic
  35338. substitution
  35339. review@
  35340. pyrimidines
  35341. pyrrolidine
  35342. quang
  35343. review
  35344. dipolar
  35345. cycloaddition
  35346. allene
  35347. diazo
  35348. dipole@
  35349. quinuclidine
  35350. synthesis
  35351. modification
  35352. oxide
  35353. deprotonatio@
  35354. radical
  35355. radical
  35356. addition
  35357. cyclization@
  35358. radical
  35359. cyclization
  35360. target
  35361. alkaloid@
  35362. radical
  35363. hydrazone
  35364. amino
  35365. cyclization
  35366. samarium
  35367. iodide
  35368. heteroat@
  35369. radicals
  35370. ranganathan
  35371. cycloaddition
  35372. ketene
  35373. diels
  35374. alder
  35375. synthesis
  35376. reaction
  35377. reaction
  35378. rates
  35379. force
  35380. field
  35381. carbenium
  35382. derivatives@
  35383. reactions
  35384. reactions/asymmetric@
  35385. reactive
  35386. reagent
  35387. carboxylic
  35388. chiral
  35389. alcohol
  35390. cyclic
  35391. b-unsaturated
  35392. ketone
  35393. cyclic
  35394. imine
  35395. cyclic
  35396. urethane
  35397. cyclohexadiene
  35398. deutero
  35399. alcohol
  35400. diester
  35401. olefin
  35402. epoxide
  35403. exocylic
  35404. olefin
  35405. hyroxy
  35406. alkene
  35407. lactone
  35408. alcohol
  35409. lactone
  35410. pyrrolidine
  35411. sulfoxyl
  35412. diene
  35413. tetrahydropyran
  35414. preparatio
  35415. preparation
  35416. preparation
  35417. experimental
  35418. sulfone
  35419. alkene
  35420. alumina
  35421. halogen
  35422. preparations
  35423. preparations
  35424. preparations
  35425. preparative
  35426. preparing
  35427. preparing
  35428. alpha
  35429. lithiosilanes
  35430. bromocyclopropyltrim
  35431. derivat
  35432. presented
  35433. pressure
  35434. pressure
  35435. effects
  35436. pretazettine
  35437. prevost
  35438. priebe
  35439. primary
  35440. primary
  35441. amines
  35442. principle
  35443. principle
  35444. stereoelectronic
  35445. stereochem
  35446. review
  35447. least
  35448. motion
  35449. prins
  35450. prins
  35451. pinacol
  35452. rearrangement
  35453. procedures
  35454. process
  35455. processes
  35456. prochiral
  35457. product
  35458. products
  35459. progenitor
  35460. progeny
  35461. program
  35462. proline
  35463. proline
  35464. derivative
  35465. decarboxylation
  35466. iminium
  35467. mannich
  35468. promoted
  35469. promoter
  35470. propanation
  35471. propargyl
  35472. propargyl
  35473. carbonates
  35474. neutral
  35475. conditions
  35476. carbonucleophiles
  35477. propargyl
  35478. cations
  35479. nicholas
  35480. reaction
  35481. propargyl
  35482. cations
  35483. synthetic
  35484. routes
  35485. cyclization
  35486. tetrahydrofur
  35487. propargyl
  35488. ether
  35489. system
  35490. stereocontrolled
  35491. synthesis
  35492. propargyl
  35493. ethers
  35494. rearrangement
  35495. propargyl
  35496. halide
  35497. propargyl
  35498. halide
  35499. elimination
  35500. vinylidene
  35501. carbene
  35502. allene
  35503. alcoh
  35504. propargyl
  35505. lithium
  35506. propargyl
  35507. mesylate
  35508. propargylene
  35509. propargylic
  35510. propargylic
  35511. alcohol
  35512. synthesis
  35513. propargylic
  35514. silanes
  35515. allylsilanes
  35516. propellane
  35517. propellanes
  35518. properties
  35519. property
  35520. propionate
  35521. propionic
  35522. proposed
  35523. propyleine
  35524. propylzinc
  35525. propynyl
  35526. prostaglandin
  35527. prostaglandin
  35528. cyclopentenone
  35529. cuprate
  35530. alkylation
  35531. review
  35532. intro
  35533. prostaglandins
  35534. prosthetic
  35535. protease
  35536. protected
  35537. protected
  35538. 13-diketone
  35539. protected
  35540. peptide
  35541. fragments
  35542. phase
  35543. synthesis
  35544. generation
  35545. diver
  35546. protecting
  35547. protecting
  35548. group
  35549. protecting
  35550. group
  35551. dimethylacetonide
  35552. protecting
  35553. group
  35554. diphenyl
  35555. silyl
  35556. protecting
  35557. group
  35558. indole
  35559. protecting
  35560. group
  35561. methyl
  35562. ether
  35563. protecting
  35564. group
  35565. ketal
  35566. protecting
  35567. groups
  35568. protection
  35569. protection
  35570. protection
  35571. deprotection
  35572. amine
  35573. review
  35574. protection
  35575. deprotection
  35576. protecting
  35577. group
  35578. selective
  35579. protection
  35580. ketone
  35581. deprotection
  35582. ketal
  35583. oxathia
  35584. anion
  35585. protection
  35586. acetylene
  35587. protection
  35588. allylic
  35589. alcohol
  35590. protection
  35591. amines
  35592. group
  35593. protection
  35594. protection
  35595. ketone
  35596. aldehyde
  35597. protein
  35598. protein
  35599. dimerization
  35600. protonated
  35601. protonation
  35602. protoporphyrin
  35603. prototropic
  35604. proudcts
  35605. provide
  35606. proximity
  35607. pschorr
  35608. pseudoesters
  35609. pseudomonas
  35610. pseudomonas
  35611. putida
  35612. enantiodivergent
  35613. synthesis
  35614. enantioselecti
  35615. pseudomonic
  35616. psychoactive
  35617. psychoactive
  35618. compounds
  35619. parkinsons
  35620. disease
  35621. chromatography
  35622. pteridines
  35623. ptychodiscus
  35624. pulsed
  35625. pummerer
  35626. pummerer
  35627. reaction
  35628. pummerer
  35629. rearrangement
  35630. pummerer
  35631. rearrangement
  35632. thermal
  35633. reactions
  35634. capture
  35635. pummerer
  35636. rearrangement
  35637. provide
  35638. cyclopropane
  35639. pummerer
  35640. review
  35641. sulfoxide
  35642. sulfonium
  35643. stereochem
  35644. diastereochem
  35645. pummerer
  35646. reaction
  35647. allylic
  35648. alcohols
  35649. charge
  35650. reversal
  35651. purification
  35652. purities
  35653. purity
  35654. putida
  35655. pyran
  35656. pyrane
  35657. pyrane
  35658. chromenes
  35659. xanthenes
  35660. flavenes
  35661. isoflavenes
  35662. flavan
  35663. benzo
  35664. pyranones
  35665. pyranosides
  35666. pyranosidic
  35667. pyrans
  35668. pyrazine
  35669. pyrazines
  35670. pyrazines
  35671. quinoxalines
  35672. phenazines
  35673. pyrazinopyrazines
  35674. pyrazinopyridazines
  35675. pyrazinopyrimidines
  35676. pyrazole
  35677. pyrazolenines
  35678. pyrazoles
  35679. pyrazoles
  35680. isoxazoles
  35681. isothiazoles
  35682. imidazoles
  35683. oxazoles
  35684. thiazo
  35685. pyrazolidine
  35686. pyrazolidinediones
  35687. pyrazolidines
  35688. pyrazolidinones
  35689. pyrazolidone
  35690. pyrazolines
  35691. pyrazolinones
  35692. pyrazolo
  35693. pyrazolo
  35694. indole
  35695. derivatives
  35696. infrared
  35697. spectroscopy
  35698. mitsu
  35699. pyrazoloimidazoles
  35700. pyrazolones
  35701. pyrazolophanes
  35702. pyrazolopyrazines
  35703. pyrazolopyrazoles
  35704. pyrazolopyridazines
  35705. pyrazolopyridines
  35706. pyrazolopyridines
  35707. pyrazolopyrimidines
  35708. pyrazolotriazines
  35709. pyrazolopyrimidines
  35710. pyrazolothiadiazoles
  35711. pyrazolothiazoles
  35712. pyrazolotriazines
  35713. pyrazolotriazoles
  35714. pyrenophorin
  35715. pyridazine
  35716. pyridazines
  35717. pyridazinopyridazine
  35718. pyridazinopyridazine
  35719. pyrimidopyridazines
  35720. pyrazinopyridazines
  35721. pyridine
  35722. pyridine
  35723. pyridine
  35724. heteroaromatic
  35725. substitution
  35726. review
  35727. pyridine
  35728. lithiation
  35729. short
  35730. efficient
  35731. alkaloid
  35732. synthesis
  35733. targe
  35734. pyridine
  35735. metalation
  35736. pyridine
  35737. reduction
  35738. pyridinepropenoic
  35739. pyridinepropenoic
  35740. ethyl
  35741. ester
  35742. pyridines
  35743. pyridines
  35744. hydroxypyridines
  35745. pyridones
  35746. quinolines
  35747. isoquinoline
  35748. pyridines
  35749. pyrimidines
  35750. pyridazines
  35751. pyrazines
  35752. triazines
  35753. tetraz
  35754. pyridinium
  35755. pyridinium
  35756. cations
  35757. pyridinones
  35758. quinolines
  35759. quinolinones
  35760. pyridinium
  35761. pyridinium
  35762. ylide
  35763. diazo
  35764. carbene
  35765. rearrangement
  35766. amine
  35767. pyridine
  35768. pyridinones
  35769. pyridinophanes
  35770. pyridoindazoles
  35771. pyridoindoles
  35772. pyridones
  35773. pyridopyrazines
  35774. pyridopyridazines
  35775. pyridopyrimidines
  35776. pyridopyrimidines
  35777. pyridopyridazines
  35778. pyridopyrazines
  35779. pyrimidine
  35780. pyrimidine
  35781. synthesis
  35782. pyrimidines
  35783. pyrimidines
  35784. pyrimidinethiones
  35785. pyrimidinone
  35786. pyrimidinone
  35787. metalation
  35788. pyrimidinones
  35789. pyrimidinophanes
  35790. pyrimidopyridazines
  35791. pyrimidopyrimidines
  35792. pyrolizidine
  35793. pyrollidine
  35794. pyrollizidine
  35795. pyrolysis
  35796. pyrone
  35797. pyrrole
  35798. chemistry
  35799. derivatives
  35800. pyrrole
  35801. osmium
  35802. complex
  35803. cycloaddition
  35804. indole
  35805. course
  35806. alkaloid
  35807. pyrrole
  35808. vinyl
  35809. sulfone
  35810. cycloaddition
  35811. arylation
  35812. raney
  35813. pyrrole-1-carboxylic
  35814. pyrrolenines
  35815. pyrroles
  35816. pyrroles
  35817. furans
  35818. thiophenes
  35819. seleno
  35820. henes
  35821. tellurophenes
  35822. indole
  35823. pyrroles
  35824. furans
  35825. thiophenes
  35826. selenophenes
  35827. tellurophenes
  35828. indole
  35829. pyrrolic
  35830. pyrrolic
  35831. compounds
  35832. shale
  35833. oxidative
  35834. cyclization
  35835. bilenes
  35836. pyrrolidin
  35837. pyrrolidine
  35838. pyrrolidine
  35839. pyrrolidine
  35840. synthesis
  35841. pyrrolidine
  35842. writing
  35843. introduction
  35844. references
  35845. review
  35846. diene
  35847. pyrrolidines
  35848. pyrrolidinol
  35849. pyrrolidinone
  35850. pyrrolidone
  35851. pyrroline
  35852. pyrrolines
  35853. pyrrolizidine
  35854. pyrrolizidine
  35855. alkaloids
  35856. terpene
  35857. derivatives
  35858. senecio
  35859. constitu
  35860. pyrrolizine
  35861. pyrrolo
  35862. pyrroloimidazoles
  35863. pyrrolooxazoles
  35864. pyrrolophanes
  35865. pyrrolopyrans
  35866. pyrrolopyrazines
  35867. pyrrolopyrazoles
  35868. pyrrolopyrazoles
  35869. thienopyrazoles
  35870. thienoisothiazoles
  35871. pyrazolo
  35872. pyrrolopyridines
  35873. pyrrolopyridines
  35874. pyridoindoles
  35875. carbolines
  35876. pyrrolopyrans
  35877. pyrrolopyrimidines
  35878. pyrrolopyrroles
  35879. pyrrolothiazoles
  35880. pyrrolothiopyrans
  35881. pyrylium
  35882. qinghaosu
  35883. quang
  35884. quang
  35885. review
  35886. dipolar
  35887. cycloaddition
  35888. allene
  35889. diazo
  35890. dipole
  35891. quassinoid
  35892. quaterary
  35893. quaterary
  35894. centre
  35895. quaternary
  35896. quaternary
  35897. carbon
  35898. quaternary
  35899. stereogenic
  35900. centers
  35901. chiral
  35902. aldehydes
  35903. diastereosel
  35904. quebrachitol
  35905. quinaldine
  35906. quinazoline
  35907. quinic
  35908. quinidine
  35909. quinine
  35910. quinkert
  35911. quinkert
  35912. review
  35913. asymmetric
  35914. chiral
  35915. induction
  35916. resolution
  35917. stere
  35918. quinodimethane
  35919. quinoline
  35920. quinoline
  35921. metalation
  35922. quinoline
  35923. reduction
  35924. quinolines
  35925. quinolines
  35926. pyridines
  35927. acridines
  35928. phenanthridines
  35929. isoquinolines
  35930. quinolinones
  35931. quinolinophanes
  35932. quinolizidine
  35933. quinolone
  35934. quinolone
  35935. metalation
  35936. quinomethane
  35937. quinone
  35938. quinonoid
  35939. quinoxaline
  35940. quinoxalines
  35941. quinuclidine
  35942. quinuclidine
  35943. synthesis
  35944. modification
  35945. oxide
  35946. deprotonatio
  35947. williams
  35948. amino
  35949. chiral
  35950. review
  35951. r-c-c-c
  35952. r-cox
  35953. r-no2
  35954. r-s-r
  35955. r-so2
  35956. r2ntf
  35957. r3po3
  35958. r3sih
  35959. r3snh
  35960. rabideau
  35961. rabideau
  35962. birch
  35963. reduction
  35964. aromatic
  35965. review
  35966. racemate
  35967. racemic
  35968. racemization
  35969. radicalD
  35970. radical
  35971. radical
  35972. addition
  35973. cyclization
  35974. radical
  35975. alkylation
  35976. radical
  35977. allylation
  35978. radical
  35979. anion
  35980. radical
  35981. anion
  35982. cyclization
  35983. radical
  35984. captodative
  35985. review
  35986. mesomeric
  35987. stable
  35988. sustman
  35989. radical
  35990. cation
  35991. radical
  35992. cation
  35993. cyclopropane
  35994. cyclopropyl
  35995. opening
  35996. radical
  35997. chain
  35998. reactions
  35999. organic
  36000. synthesis
  36001. design
  36002. radical
  36003. chemistry
  36004. radical
  36005. clock
  36006. bioorganic
  36007. introduction
  36008. writing
  36009. rearr
  36010. radical
  36011. clock
  36012. cyclopropyl
  36013. carbinyl
  36014. opening
  36015. review
  36016. radical
  36017. cyclization
  36018. adduct
  36019. opening
  36020. radical
  36021. radical
  36022. cyclization
  36023. acetals
  36024. ethers
  36025. radical
  36026. cyclization
  36027. alcohol
  36028. reagent
  36029. sulfur
  36030. carbonyl
  36031. radical
  36032. cyclization
  36033. review
  36034. synthesis
  36035. target
  36036. retrosynthesis
  36037. radical
  36038. cyclization
  36039. intramolecular
  36040. target
  36041. ketyl
  36042. heterocy
  36043. radical
  36044. cyclization
  36045. target
  36046. alkaloid
  36047. radical
  36048. deoxygenation
  36049. radical
  36050. deoxygenation
  36051. selenocarbonate
  36052. radical
  36053. desulfurization
  36054. hydrazone
  36055. amino
  36056. cyclization
  36057. samarium
  36058. iodide
  36059. heteroat
  36060. radical
  36061. probes
  36062. grignard
  36063. reagents
  36064. benzophenone
  36065. mechanism
  36066. radical
  36067. nitrogen
  36068. aminyl
  36069. cyclization
  36070. pyrrolidine
  36071. review
  36072. radical
  36073. oxime
  36074. cyclization
  36075. radical
  36076. reaction
  36077. radical
  36078. reactions
  36079. radical
  36080. rearrangement
  36081. radical
  36082. reduction
  36083. radical
  36084. reduction
  36085. phenyl
  36086. silane
  36087. radical
  36088. closure
  36089. radical
  36090. stereochem
  36091. silicon
  36092. cyclization
  36093. review
  36094. acetal
  36095. radical
  36096. target
  36097. ketene
  36098. cyclobutanone
  36099. manganese
  36100. copper
  36101. radical
  36102. transfer
  36103. chiral
  36104. asymmetric
  36105. selenium
  36106. group
  36107. felkin
  36108. radical
  36109. trapping
  36110. reaction
  36111. radicals
  36112. radicals
  36113. radicals
  36114. cyclobutanes
  36115. radii
  36116. radom
  36117. radom
  36118. diazo
  36119. ketone
  36120. wolff
  36121. rearrangement
  36122. oxirene
  36123. carbene
  36124. rajappa
  36125. rajappa
  36126. enamine
  36127. nitro
  36128. preparation
  36129. diels
  36130. alder
  36131. heterocycle
  36132. ramaiah
  36133. ramaiah
  36134. review
  36135. annelation
  36136. cyclopentane
  36137. synthesis
  36138. wittig
  36139. ramaih
  36140. ramaih
  36141. annelation
  36142. enone
  36143. review
  36144. cyclopentenone
  36145. ramberg
  36146. ramberg
  36147. blacklund
  36148. reaction
  36149. ramberg-backlund
  36150. ramberg-bcklund
  36151. rameichanauran
  36152. ramsden
  36153. ramsden
  36154. dipole
  36155. cycloaddition
  36156. zwitterion
  36157. heterocycle
  36158. mesoioni
  36159. ramsden
  36160. mesoionic
  36161. heterocycle
  36162. zwitterion
  36163. dipole
  36164. cycloadditio
  36165. raney
  36166. raney
  36167. nickel
  36168. raney-nickel
  36169. ranganathan
  36170. ranganathan
  36171. cycloaddition
  36172. ketene
  36173. diels
  36174. alder
  36175. synthesis
  36176. ransformation
  36177. ransformations
  36178. epoxide
  36179. oxirane
  36180. preparation
  36181. epoxidation
  36182. chiral
  36183. review
  36184. rapamycin
  36185. rapid
  36186. earth
  36187. catayst
  36188. system
  36189. odology
  36190. alkylation
  36191. silicon
  36192. revie
  36193. constants
  36194. constants
  36195. rearrangements
  36196. cyclopropylmethyl
  36197. rates
  36198. rather
  36199. rawal
  36200. rawal
  36201. azide
  36202. ester
  36203. conversion
  36204. diethylaluminum
  36205. aluminum
  36206. crystal
  36207. structure
  36208. reactivity
  36209. imines
  36210. crystal
  36211. structure
  36212. expansion
  36213. photoadducts
  36214. alkenes
  36215. rbring
  36216. react
  36217. reacti
  36218. reactio
  36219. reaction
  36220. reaction
  36221. reaction
  36222. reactions
  36223. reactions
  36224. tions/asymmetric
  36225. reactions/promoted
  36226. reactions/resemble
  36227. reactive
  36228. reactive
  36229. reactivity
  36230. reactivity
  36231. nitrones
  36232. reactivity/allylic
  36233. reactivity/cyclo-add
  36234. reagent
  36235. reagent
  36236. rmylation
  36237. metal
  36238. complex
  36239. reagents
  36240. reagents
  36241. reagents
  36242. acylation
  36243. formylation
  36244. reagents
  36245. ransformation
  36246. stereochemistry
  36247. enzymes
  36248. reduction
  36249. reagents
  36250. biotransformation
  36251. reagents
  36252. bu3snh
  36253. tribut
  36254. hydride
  36255. hydrometallation
  36256. reagents
  36257. oxidation
  36258. c-c-oh
  36259. reagents
  36260. thexylborane
  36261. alkenes
  36262. dienes
  36263. acids
  36264. reagents
  36265. fluoride
  36266. reagents
  36267. carbon
  36268. suboxide
  36269. reagents
  36270. catalysts
  36271. solvents
  36272. quaternary
  36273. ammonium
  36274. reagents
  36275. catecholborane
  36276. hydrometallation
  36277. reagents
  36278. ccl3cho
  36279. c-ccl3
  36280. chloral
  36281. reagents
  36282. chiral
  36283. auxiliary
  36284. chiral
  36285. catalyst
  36286. binap
  36287. reagents
  36288. chloramine
  36289. reagents
  36290. chlorosulfonyl
  36291. isocyanate
  36292. n-so2cl
  36293. heterocycles
  36294. reagents
  36295. carbon
  36296. disulfide
  36297. reagents
  36298. cyanotrimethylsilane
  36299. diastereoselectivity
  36300. nitriles
  36301. reagents
  36302. amidines
  36303. elimination
  36304. reagents
  36305. diazometane
  36306. reagents
  36307. diethylaminosulfur
  36308. trifluoride
  36309. aminofluorosulfurane
  36310. reagents
  36311. 4-dimethylaninopyrid
  36312. acylation
  36313. reagents
  36314. fluorides
  36315. reagents
  36316. functional
  36317. groups
  36318. oxidation
  36319. alkynes
  36320. alkenes
  36321. reagents
  36322. functional
  36323. groups
  36324. oxidation
  36325. miscellaneous
  36326. potassium
  36327. reagents
  36328. dimethylsulfoxonium
  36329. methylide
  36330. corey's
  36331. reagents
  36332. halogenation
  36333. oxidation
  36334. arylation
  36335. reagents
  36336. halogenation
  36337. oxidation
  36338. arylation
  36339. reagents
  36340. hexamethylenetetrami
  36341. amination
  36342. formylation
  36343. reagents
  36344. hooc-c-x
  36345. rooc-c-x
  36346. nitroacetic
  36347. nitroace
  36348. reagents
  36349. hydrazine
  36350. reagents
  36351. hydroxylamine-o-sulf
  36352. amination
  36353. reductive
  36354. deami
  36355. reagents
  36356. iodine
  36357. azide
  36358. azirines
  36359. reagents
  36360. lawesson's
  36361. reagent
  36362. reagents
  36363. lithium
  36364. triethylborohydride
  36365. super
  36366. hydride
  36367. l-selectr
  36368. reagents
  36369. malononitrile
  36370. cyanoacetamide
  36371. alpha-cyanothioaceta
  36372. reagents
  36373. me3sii
  36374. iodotrimethylsilane
  36375. trimethyliodosilane
  36376. reagents
  36377. methyl
  36378. isothiocyanate
  36379. reaction
  36380. reagents
  36381. naftion-h
  36382. reagents
  36383. naio4
  36384. periodic
  36385. periodates
  36386. oxidation
  36387. reagents
  36388. nitrosonium
  36389. salts
  36390. oxidation
  36391. reagents
  36392. phosgene
  36393. cocl2
  36394. reagents
  36395. o-mesitylenesulfonyl
  36396. amination
  36397. reagents
  36398. oxonium
  36399. alkylation
  36400. reagents
  36401. photochemical
  36402. reactions
  36403. photochemistry
  36404. singlet
  36405. reagents
  36406. supported
  36407. catalysts
  36408. reagents
  36409. reduction
  36410. dibal
  36411. tribal
  36412. diisobutylaluminium
  36413. hydride
  36414. reagents
  36415. reduction
  36416. sodium
  36417. cyanoborohydride
  36418. nabh3cn
  36419. reagents
  36420. sulfur
  36421. tetrafluoride
  36422. fluorination
  36423. fluorid
  36424. reagents
  36425. reagents
  36426. socl2
  36427. thionyl
  36428. chloride
  36429. reagents
  36430. solvents
  36431. catalysts
  36432. diazabicycloundecene
  36433. reagents
  36434. solvents
  36435. catalysts
  36436. reagents
  36437. solvents
  36438. catalysts
  36439. reagents
  36440. solvents
  36441. catalysts
  36442. reagents
  36443. solvents
  36444. catalysts
  36445. peroxydisulfate
  36446. electron
  36447. transfe
  36448. reagents
  36449. stereochemistry
  36450. asymmetric
  36451. catalysis
  36452. reagents
  36453. stereochemistry
  36454. configuration
  36455. reagents
  36456. superoxide
  36457. reagents
  36458. superoxide
  36459. reagents
  36460. t-buok
  36461. me3cok
  36462. potassium
  36463. t-butoxide
  36464. reagents
  36465. ticl4
  36466. titanium
  36467. tetrachloride
  36468. reagents
  36469. tmscl
  36470. trimethylchlorosilan
  36471. reagents
  36472. triflic
  36473. cf3so2x
  36474. cf3so3h
  36475. reagents
  36476. triflic
  36477. f3cso2x
  36478. f3cso3h
  36479. rearrangeme
  36480. rearrangementE
  36481. reagents
  36482. reduction
  36483. dibal
  36484. tribal
  36485. diisobutylaluminium
  36486. hydride
  36487. rearrangement
  36488. rearrangement
  36489. catalysis
  36490. chloride
  36491. ring@
  36492. reduced@
  36493. reductase@
  36494. reduction
  36495. reduction
  36496. bond@
  36497. derivatives
  36498. anthracyclinone
  36499. anthraquin@
  36500. reiser
  36501. allyl
  36502. palladium
  36503. asymmetric
  36504. review
  36505. allylic
  36506. substi@
  36507. resolved
  36508. photoacoustic
  36509. calorimetry
  36510. laser
  36511. photochemistry
  36512. review
  36513. review
  36514. baldwin's
  36515. rules
  36516. stereoelectronic
  36517. closure@
  36518. review
  36519. cyclization
  36520. stereoselectivity
  36521. cyclic
  36522. acyclic
  36523. vinyl
  36524. review
  36525. nickel
  36526. organometallic
  36527. cyclization
  36528. allylic
  36529. closur@
  36530. review
  36531. synthesis
  36532. cyclization
  36533. cycloaddition
  36534. thebtaranoth@
  36535. rhodium
  36536. rhodium
  36537. transition
  36538. metal
  36539. catalyst@
  36540. closure
  36541. reactions
  36542. membered
  36543. rings
  36544. alkali
  36545. metal
  36546. bifu@
  36547. ripoll
  36548. cycloreversion
  36549. synthesis
  36550. heterocycle
  36551. carbocycle
  36552. retro@
  36553. route
  36554. ruthenium
  36555. carbene
  36556. transition
  36557. metal
  36558. complex
  36559. rearrangement
  36560. rearrangement
  36561. earrangement
  36562. rearrangement
  36563. route
  36564. rearrangement
  36565. substituent
  36566. alkoxides
  36567. rearrangements
  36568. rearrangements
  36569. alkyllithiums
  36570. rearrangements
  36571. cycloaddition
  36572. recent
  36573. receptor
  36574. recognition
  36575. reconstitutive
  36576. reconstitutive
  36577. condensation
  36578. red-al
  36579. red-al
  36580. reduction
  36581. redox
  36582. reduc
  36583. reduce
  36584. reduced
  36585. reduced
  36586. peptide
  36587. solid
  36588. phase
  36589. synthesis
  36590. analogs
  36591. backbone
  36592. reducing
  36593. reducing
  36594. reagent
  36595. reduction
  36596. reduction
  36597. b-unsaturated
  36598. ketone
  36599. reduction
  36600. imine
  36601. reduction
  36602. ketone
  36603. reductive
  36604. acylation
  36605. reductive
  36606. alkylation
  36607. reductive
  36608. alkylation
  36609. diastereoselection
  36610. vinylsilanes
  36611. inducti
  36612. reductive
  36613. carbonylation
  36614. azides
  36615. reductive
  36616. cleavage
  36617. cycloadditions
  36618. alkaloids
  36619. reductive
  36620. coupling
  36621. reductive
  36622. cyclization
  36623. reductive
  36624. decyanation
  36625. tactic
  36626. reductive
  36627. lithiation
  36628. reductive
  36629. expansion
  36630. redutive
  36631. azete
  36632. cycloaddition
  36633. heterocycle
  36634. review
  36635. benzazete
  36636. extrus
  36637. reetz
  36638. reetz
  36639. lewis
  36640. alkylation
  36641. silicon
  36642. review
  36643. synthesis
  36644. reetz
  36645. review
  36646. amino
  36647. stereoselective
  36648. diels
  36649. alder
  36650. wittig
  36651. reference
  36652. references
  36653. reformatsky
  36654. reformatsky
  36655. reaction
  36656. facile
  36657. synthesis
  36658. reformatsky
  36659. reagents
  36660. regio
  36661. regiochem
  36662. regiochemical
  36663. regiochemical
  36664. control
  36665. chelating
  36666. processes
  36667. oxides
  36668. regiochemical
  36669. control
  36670. derivatives
  36671. anthracyclinone
  36672. anthraquin
  36673. regiochemistry
  36674. regiocontrol
  36675. regioreversed
  36676. regioselective
  36677. regioselective
  36678. acylation
  36679. selectivity
  36680. regiospecific
  36681. regiospecific
  36682. synthesis
  36683. anthracyclinones
  36684. efficient
  36685. regiospecific
  36686. synthesis
  36687. organic
  36688. synthesis
  36689. cycloaddition
  36690. regiospecific
  36691. synthesis
  36692. substituted
  36693. quinones
  36694. cyclobutenedion
  36695. regitz
  36696. regitz
  36697. review
  36698. diazo
  36699. diazoalkane
  36700. electrophilic
  36701. substitution
  36702. reich
  36703. reich
  36704. reagent
  36705. organometallic
  36706. selenium
  36707. review
  36708. addition
  36709. alkene
  36710. reich
  36711. review
  36712. silicon
  36713. target
  36714. synthesis
  36715. writing
  36716. epoxide
  36717. cyclobutenone
  36718. reaction
  36719. enone
  36720. review
  36721. displacem
  36722. reimer-tiemann
  36723. reinecke
  36724. reinecke
  36725. review
  36726. benzyne
  36727. hetaryne
  36728. alkyne
  36729. strain
  36730. reiser
  36731. reiser
  36732. allyl
  36733. palladium
  36734. asymmetric
  36735. review
  36736. allylic
  36737. substi
  36738. reissig
  36739. reissig
  36740. siloxyl
  36741. cyclopropane
  36742. opening
  36743. desilylation
  36744. homoe
  36745. related
  36746. relationship
  36747. relative
  36748. reluctant
  36749. remarkably
  36750. remarkably
  36751. simple
  36752. synthesis
  36753. remote
  36754. remote
  36755. asymmetric
  36756. induction
  36757. wittig
  36758. contraction
  36759. alpha
  36760. remote
  36761. stereogenic
  36762. center
  36763. enantioselective
  36764. synthesis
  36765. conform
  36766. removal
  36767. renes
  36768. renin
  36769. reogenic
  36770. reparations
  36771. replacement
  36772. representative
  36773. requirements
  36774. resctions
  36775. resemble
  36776. resemble
  36777. grandfather
  36778. glucose
  36779. diels
  36780. alder
  36781. reactions
  36782. unsatu
  36783. residues
  36784. resin
  36785. resins
  36786. resolutio
  36787. resolution
  36788. resolutions
  36789. resolved
  36790. resolved
  36791. photoacoustic
  36792. calorimetry
  36793. laser
  36794. photochemistry
  36795. resonance
  36796. ressig
  36797. restricted
  36798. restriction
  36799. retention
  36800. retro
  36801. aldol
  36802. reaction
  36803. retro
  36804. elimination
  36805. mechanism
  36806. retro
  36807. diels-alder
  36808. retroaldol
  36809. retronecine
  36810. retrosynthesis
  36811. retrosynthesis
  36812. analysis
  36813. review
  36814. synthesis
  36815. retro
  36816. teaching
  36817. retrosynthetic
  36818. return
  36819. reversal
  36820. reverse
  36821. reverse
  36822. transcriptase
  36823. heterocyclic
  36824. quinones
  36825. streptonigrin
  36826. reversible
  36827. reviewD
  36828. review
  36829. review
  36830. review
  36831. review
  36832. review
  36833. review
  36834. ketene
  36835. cyclobutanone
  36836. intramolecular
  36837. vinyl
  36838. mangane
  36839. review
  36840. anion
  36841. equivalent
  36842. cyanohydrin
  36843. nitrile
  36844. amine
  36845. alcoh
  36846. review
  36847. amaryllidaceae
  36848. sceletium
  36849. alkaloids
  36850. review
  36851. amide
  36852. nitro
  36853. carbanion
  36854. dipole
  36855. stabilized
  36856. alkylation
  36857. review
  36858. amine
  36859. steric
  36860. hindrance
  36861. nitrogen
  36862. harpoon
  36863. review
  36864. aminyl
  36865. radicals
  36866. pyrrolidine
  36867. synthesis
  36868. review
  36869. baldwin's
  36870. rules
  36871. stereoelectronic
  36872. closure
  36873. review
  36874. borane
  36875. silane
  36876. grignard
  36877. reagent
  36878. organo
  36879. lithium
  36880. isotope
  36881. review
  36882. carbanion
  36883. chelation
  36884. reagent
  36885. review
  36886. carbenoid
  36887. fischer
  36888. complex
  36889. cyclisation
  36890. ylide
  36891. amine
  36892. review
  36893. carbon
  36894. monoxide
  36895. organometallic
  36896. complex
  36897. metal
  36898. werne
  36899. review
  36900. catalyst
  36901. organometallic
  36902. reagent
  36903. chiral
  36904. asymmetric
  36905. review
  36906. catalyst
  36907. phase
  36908. transfer
  36909. dichloro
  36910. preparation
  36911. carbene
  36912. review
  36913. cation
  36914. radical
  36915. cycloaddition
  36916. sigmatropic
  36917. diels
  36918. alder
  36919. review
  36920. chiral
  36921. induction
  36922. asymmetric
  36923. cycloaddition
  36924. synthesis
  36925. review
  36926. chiral
  36927. induction
  36928. bicyclic
  36929. camphor
  36930. sultam
  36931. asymmetric
  36932. review
  36933. cohen
  36934. epoxide
  36935. reductive
  36936. cleavage
  36937. regioselective
  36938. review
  36939. column
  36940. pirkle
  36941. chromatography
  36942. separation
  36943. enantiomer
  36944. review
  36945. conformation
  36946. allyl
  36947. stereochem
  36948. strain
  36949. boltzmann
  36950. review
  36951. conjugate
  36952. addition
  36953. cuprate
  36954. enone
  36955. trapping
  36956. electr
  36957. review
  36958. coupling
  36959. cross
  36960. palladium
  36961. catalyst
  36962. silicon
  36963. silyl
  36964. hyper
  36965. review
  36966. cyclization
  36967. stereoselectivity
  36968. cyclic
  36969. acyclic
  36970. vinyl
  36971. review
  36972. elimination
  36973. reagent
  36974. review
  36975. diels
  36976. alder
  36977. cycloaddition
  36978. reaction
  36979. asymmetric
  36980. review
  36981. dithiane
  36982. carbanion
  36983. alkylation
  36984. deprotection
  36985. hydrolysis
  36986. review
  36987. electron
  36988. transfer
  36989. electrocyclization
  36990. diels
  36991. alder
  36992. review
  36993. epoxide
  36994. diazo
  36995. photolysis
  36996. ylide
  36997. oxonium
  36998. carbenoid
  36999. review
  37000. epoxide
  37001. oxirane
  37002. opening
  37003. synthesis
  37004. nucleophilic
  37005. review
  37006. chemoselectivity
  37007. regiochem
  37008. select
  37009. review
  37010. hydrazine
  37011. amine
  37012. oxidation
  37013. diimide
  37014. review
  37015. iminium
  37016. alkaloid
  37017. stereoselective
  37018. alkyne
  37019. overman
  37020. rearr
  37021. review
  37022. induction
  37023. chiral
  37024. asymmetric
  37025. chiral
  37026. sulfoxide
  37027. vinyl
  37028. review
  37029. isobenzofuran
  37030. methodology
  37031. diels
  37032. alder
  37033. target
  37034. synthesi
  37035. review
  37036. ketone
  37037. enolate
  37038. mechanism
  37039. stereoselectivity
  37040. stere
  37041. review
  37042. lactam
  37043. rearrangement
  37044. regioselective
  37045. expansion
  37046. review
  37047. methodology
  37048. catalyst
  37049. phase
  37050. transfer
  37051. review
  37052. nickel
  37053. organometallic
  37054. cyclization
  37055. allylic
  37056. closur
  37057. review
  37058. spectroscopy
  37059. mechanism
  37060. physical
  37061. organic
  37062. dioxetane
  37063. review
  37064. oxazoles
  37065. alfred
  37066. hassner
  37067. review
  37068. palladium
  37069. synthesis
  37070. allyl
  37071. complex
  37072. methodology
  37073. tsuji
  37074. review
  37075. phosphorus
  37076. application
  37077. synthesis
  37078. reactivity
  37079. reaction
  37080. review
  37081. preparation
  37082. thiophosgene
  37083. thioamide
  37084. halide
  37085. amide
  37086. review
  37087. pressure
  37088. ultra
  37089. sound
  37090. cycloaddition
  37091. synthesis
  37092. writing
  37093. review
  37094. reagent
  37095. counterattack
  37096. synthesis
  37097. review
  37098. reagent
  37099. ketene
  37100. heteroatom
  37101. acetal
  37102. ketene
  37103. acetal
  37104. cycloa
  37105. review
  37106. silicon
  37107. naked
  37108. fluoride
  37109. reagent
  37110. review
  37111. spiro
  37112. ketal
  37113. preparation
  37114. synthesis
  37115. carbonyl
  37116. protection
  37117. review
  37118. steric
  37119. hindrance
  37120. silicon
  37121. silyl
  37122. review
  37123. substitution
  37124. epoxide
  37125. cuprate
  37126. opening
  37127. vinyl
  37128. displ
  37129. review
  37130. sulfone
  37131. writing
  37132. carbanion
  37133. unsaturated
  37134. vinyl
  37135. cycloaddi
  37136. review
  37137. sulfonyl
  37138. asymmetric
  37139. oxidation
  37140. aziridine
  37141. hydrazine
  37142. review
  37143. sulfoxide
  37144. oxidation
  37145. sulfide
  37146. sulfur
  37147. reagent
  37148. mades
  37149. review
  37150. synthesis
  37151. cyclization
  37152. cycloaddition
  37153. thebtaranoth
  37154. review
  37155. synthesis
  37156. organometallic
  37157. sulfone
  37158. enantioselectivity
  37159. review
  37160. tetrahydrofuran
  37161. polycyclic
  37162. ether
  37163. antibiotic
  37164. spiro
  37165. review
  37166. vinyl
  37167. anion
  37168. addition
  37169. carbonyl
  37170. method
  37171. enone
  37172. drewes
  37173. review
  37174. extensive
  37175. references
  37176. types
  37177. diazo
  37178. carbo
  37179. review
  37180. zeolite
  37181. synthesis
  37182. preparation
  37183. experimental
  37184. review
  37185. bromo
  37186. condensation
  37187. addition
  37188. organometallic
  37189. carbo
  37190. reviews
  37191. revision
  37192. rganic
  37193. catalyzed
  37194. insertion
  37195. reactions
  37196. rhcl3
  37197. rhcl3
  37198. mediated
  37199. alkene
  37200. isomerization
  37201. rhodium
  37202. rhodium
  37203. rhodium
  37204. carbebe
  37205. complex
  37206. rhodium
  37207. carbene
  37208. rhodium
  37209. carbene
  37210. complex
  37211. rhodium
  37212. catalysis
  37213. olefin
  37214. orted
  37215. catalyst
  37216. metal
  37217. complexes
  37218. rhodium
  37219. catalyst
  37220. rhodium
  37221. catalyzed
  37222. carcosilation
  37223. alkynes
  37224. rhodium
  37225. complex
  37226. rhodium
  37227. cyclobutadiene
  37228. carbon
  37229. carbon
  37230. bonds
  37231. vinylcyclopropene
  37232. rhodium
  37233. diazo
  37234. carbenoid
  37235. insertion
  37236. stereochem
  37237. enantioselectiv
  37238. rhodium
  37239. diazo
  37240. ether
  37241. carbenoid
  37242. carbonyl
  37243. ylide
  37244. oxonium
  37245. rearran
  37246. rhodium
  37247. diazo
  37248. ester
  37249. acetate
  37250. acetoxy
  37251. rearrangement
  37252. rhodium
  37253. carboxylate
  37254. catalyzed
  37255. reactions
  37256. construction
  37257. rhodium
  37258. mediated
  37259. cyclotrimerization
  37260. rhodium
  37261. references
  37262. review
  37263. writing
  37264. synthesis
  37265. carbenoid
  37266. introd
  37267. rhodium
  37268. transition
  37269. metal
  37270. catalyst
  37271. rhodizonate
  37272. ribase
  37273. riboflavin
  37274. riboflavin
  37275. biotin
  37276. thiamin
  37277. vitamin
  37278. ribonolactone
  37279. ribose
  37280. rieke
  37281. rieke
  37282. magnesium
  37283. transition
  37284. metal
  37285. higher
  37286. order
  37287. cycloaddition
  37288. chromi
  37289. rigidified
  37290. field
  37291. acetals
  37292. closure
  37293. reactions
  37294. membered
  37295. rings
  37296. alkali
  37297. metal
  37298. closure
  37299. rearrangement
  37300. construction
  37301. contraction
  37302. tetrahydrofurans
  37303. lactones
  37304. enlargement
  37305. enlargement
  37306. reaction
  37307. silanes
  37308. esters
  37309. expansion
  37310. expansion
  37311. membered
  37312. heterocycles
  37313. halogenated
  37314. ketenes
  37315. expansion
  37316. fused
  37317. cyclobutanones
  37318. bicyclic
  37319. systems
  37320. group
  37321. expansion
  37322. intramolecular
  37323. functionalization
  37324. prostaglandi
  37325. expansion
  37326. constants
  37327. vinyl
  37328. cyclopropanes
  37329. kinetics
  37330. fragmentation
  37331. opening
  37332. polymerization
  37333. ruthenium
  37334. cycloolefins
  37335. metathesi
  37336. opening
  37337. reaction
  37338. alpha
  37339. amino
  37340. acids
  37341. aziridinecarboxyli
  37342. opening
  37343. reaction
  37344. thiiranes
  37345. carboxylic
  37346. derivatives
  37347. system
  37348. unsaturated
  37349. ketones
  37350. route
  37351. transfer
  37352. reaction
  37353. sigmatropic
  37354. rearrangement
  37355. transfer
  37356. reaction
  37357. occurring
  37358. fused
  37359. furans
  37360. cycloaddition
  37361. ring-chain
  37362. rings
  37363. ripoll
  37364. ripoll
  37365. cycloreversion
  37366. synthesis
  37367. heterocycle
  37368. carbocycle
  37369. retro
  37370. ripoll
  37371. retro
  37372. cycloaddition
  37373. cycloreversion
  37374. review
  37375. diels
  37376. alder
  37377. risso
  37378. ritter
  37379. rmation
  37380. rmediates
  37381. roach
  37382. roberts
  37383. robins
  37384. robins
  37385. pyrrolizidine
  37386. alkaloids
  37387. review
  37388. robinson
  37389. robinson
  37390. annulation
  37391. drimane
  37392. related
  37393. sesquiterpenes
  37394. rodrigo
  37395. rooc-c
  37396. rooc-c-cn
  37397. rooc-c-coor
  37398. rooc-c-x
  37399. rooc-n
  37400. ropellanes
  37401. roridin
  37402. rosini
  37403. rosini
  37404. carbanion
  37405. review
  37406. nitro
  37407. synthon
  37408. synthesis
  37409. alkylation
  37410. roskamp
  37411. roskamp
  37412. homologation
  37413. rosnati
  37414. rosnati
  37415. diazo
  37416. migration
  37417. carbonium
  37418. rearrangement
  37419. reaction
  37420. rossiter
  37421. rossiter
  37422. conjugate
  37423. addition
  37424. asymmetric
  37425. review
  37426. chiral
  37427. ligands
  37428. rotation
  37429. rotational
  37430. rotomer
  37431. rousch
  37432. route
  37433. route
  37434. route
  37435. polyazapentadienes
  37436. thermolysis
  37437. routes
  37438. routiennocin
  37439. roxburgh
  37440. alkylidene
  37441. complex
  37442. clusters
  37443. ligands
  37444. ruano
  37445. ruano
  37446. diels
  37447. alder
  37448. asymmetric
  37449. review
  37450. sulfoxide
  37451. lewis
  37452. rubin
  37453. rudler
  37454. rudorf
  37455. rudorf
  37456. conjugate
  37457. addition
  37458. michael
  37459. intramolecular
  37460. alkyne
  37461. rules
  37462. rutaceous
  37463. ruthenium
  37464. ruthenium
  37465. carbene
  37466. transition
  37467. metal
  37468. complex
  37469. ruthenium
  37470. catalyst
  37471. ruthenium
  37472. catalyzed
  37473. butenolide
  37474. annulation
  37475. ruthenium
  37476. complex
  37477. ruthenium
  37478. complex
  37479. catalyzed
  37480. cyclization
  37481. ruthenium
  37482. reagent
  37483. ruthenium
  37484. trifluoroacetate
  37485. sulfoximine
  37486. carbanion
  37487. addition
  37488. carbonyls
  37489. imines
  37490. acetals
  37491. halocyclopropane
  37492. electron
  37493. transfer
  37494. stereoselectivity
  37495. cyclohexane
  37496. cycloheptane
  37497. serine
  37498. s-buli
  37499. tmeda
  37500. sakurai
  37501. sakurai
  37502. alkene
  37503. silicon
  37504. silyl
  37505. review
  37506. condensation
  37507. carbonyl
  37508. salaun
  37509. salaun
  37510. salaun
  37511. cyclopropane
  37512. cyclopropanone
  37513. hemiacetal
  37514. acetal
  37515. review
  37516. salenG
  37517. salen
  37518. manganese
  37519. complexes
  37520. hydrogen
  37521. peroxide
  37522. trimethy
  37523. salicylate
  37524. salmon
  37525. salts
  37526. samarium
  37527. samarium
  37528. carbon
  37529. carbon
  37530. formation
  37531. organic
  37532. synthesis
  37533. samarium
  37534. catalyst
  37535. samarium
  37536. diiodide
  37537. samarium
  37538. iodide
  37539. barbier
  37540. reaction
  37541. salaun
  37542. samarium
  37543. iodide@
  37544. samarium
  37545. iodide
  37546. cyclization@
  37547. sauer@
  37548. schlosser's@
  37549. schmidt
  37550. rearrangement
  37551. ketones
  37552. mechanistic
  37553. discussion@
  37554. sdiene@
  37555. selective
  37556. substitution
  37557. activated
  37558. bleomycin
  37559. carbohydrate
  37560. moie@
  37561. selenium
  37562. oxide
  37563. oxidation
  37564. ethers
  37565. hexahydro
  37566. imino
  37567. benzazo@
  37568. sequential
  37569. reaction@
  37570. sesquinorbornatriene@
  37571. sharpless
  37572. catalyst@
  37573. shikimate@
  37574. silabenzene@
  37575. silacyclopentenes@
  37576. silane
  37577. reduction@
  37578. silicon
  37579. silicon
  37580. chemistry@
  37581. siloxy@
  37582. silyl
  37583. baeyer
  37584. villiger
  37585. silyl
  37586. baeyer-villiger
  37587. silyl
  37588. derivatives@
  37589. silyl
  37590. ketene
  37591. acetals
  37592. mediated
  37593. reactions
  37594. simple
  37595. diastere@
  37596. silylstannane@
  37597. single
  37598. reduction
  37599. coupling@
  37600. snider
  37601. reaction
  37602. mechanism
  37603. review
  37604. isotope
  37605. deuterium
  37606. lewis@
  37607. sodium
  37608. azide/copper
  37609. iodide@
  37610. solid
  37611. phase
  37612. carbohydrate
  37613. synthesis
  37614. sparteine
  37615. derivatives
  37616. lithiation@
  37617. samarium
  37618. iodide
  37619. cyclization
  37620. samarium
  37621. iodide
  37622. deoxygenation
  37623. samarium
  37624. iodide
  37625. sulfonamide
  37626. deprotection
  37627. samarium
  37628. iodide
  37629. reduction
  37630. samarium
  37631. ketyl
  37632. radical
  37633. samarium
  37634. trichloride
  37635. reagent
  37636. cleavage
  37637. hydrazone
  37638. sanchez
  37639. sanchez
  37640. alkaloid
  37641. writing
  37642. student
  37643. biological
  37644. review
  37645. amido
  37646. santalol
  37647. santelli
  37648. santelli
  37649. nazarov
  37650. cyclization
  37651. review
  37652. cyclopentenone
  37653. electrocy
  37654. saponification
  37655. sapra
  37656. sarkar
  37657. sarkar
  37658. allyl
  37659. silane
  37660. allylsilane
  37661. silicon
  37662. alkene
  37663. review
  37664. prepar
  37665. sasaki
  37666. sasaki
  37667. alkyne
  37668. amine
  37669. addition
  37670. heterocycle
  37671. review
  37672. writing
  37673. sativene
  37674. sativenediol
  37675. alkaloid
  37676. review
  37677. synthesis
  37678. heterocycles
  37679. pyrrolizidine
  37680. satoh
  37681. satoh
  37682. sulfoxide
  37683. review
  37684. synthesis
  37685. carbanion
  37686. epoxide
  37687. satoh
  37688. review
  37689. epoxide
  37690. sulfone
  37691. sulfonyl
  37692. sulfoxide
  37693. oxirane
  37694. saturated
  37695. saturated
  37696. hydrocarbons
  37697. functionalization
  37698. sauer
  37699. sauer
  37700. diels
  37701. alder
  37702. review
  37703. theory
  37704. regiochem
  37705. molecular
  37706. orbital
  37707. scavenger
  37708. sceletium
  37709. schaefer
  37710. schaefer
  37711. review
  37712. migration
  37713. sigmatropic
  37714. carbene
  37715. nitrene
  37716. vinyl
  37717. schaumann
  37718. schenck
  37719. schick
  37720. schiff
  37721. schiff
  37722. schiff
  37723. metal
  37724. catalyzed
  37725. epoxidation
  37726. schinzer
  37727. schinzer
  37728. allyl
  37729. silyl
  37730. propargyl
  37731. sakurai
  37732. annelation
  37733. review
  37734. schleyer
  37735. schleyer
  37736. anomeric
  37737. effect
  37738. theory
  37739. writing
  37740. introduction
  37741. student
  37742. schleyer
  37743. review
  37744. introduction
  37745. ortho
  37746. lithiation
  37747. chelation
  37748. schlosser
  37749. schlosser
  37750. review
  37751. super
  37752. schlosser
  37753. butyllithium
  37754. butoxide
  37755. schmaucks
  37756. schmaucks
  37757. schmidbaur
  37758. schmidbaur
  37759. review
  37760. ylide
  37761. silicon
  37762. phosphorous
  37763. sulfur
  37764. schmidt
  37765. schmidt
  37766. iodotrimethylsilane
  37767. desilylation
  37768. review
  37769. silyl
  37770. ether
  37771. schmidt
  37772. rearrangement
  37773. ketones
  37774. mechanistic
  37775. discussion
  37776. schollkopf
  37777. schollkopf
  37778. chiral
  37779. auxiliary
  37780. schore
  37781. schore
  37782. review
  37783. cycloaddition
  37784. metal
  37785. transition
  37786. catalyzed
  37787. alkyn
  37788. schreiber
  37789. schreiber
  37790. ozonolysis
  37791. schrock
  37792. schultz
  37793. schultz
  37794. photorearrangement
  37795. cyclization
  37796. electrocyclic
  37797. ylide
  37798. schurig
  37799. schurig
  37800. oxirane
  37801. epoxide
  37802. alkene
  37803. chiral
  37804. review
  37805. science
  37806. scission
  37807. sclerosporin
  37808. sclerosporin
  37809. enantiomers
  37810. scopadulcic
  37811. scopadulcic
  37812. scoparia
  37813. dulcis
  37814. practical
  37815. synthesis
  37816. scoparia
  37817. scope
  37818. scrambling
  37819. scrobiculatus
  37820. secodaphniphylline
  37821. secondary
  37822. secondary
  37823. secondary
  37824. alcohol
  37825. secondary
  37826. alcohols
  37827. aldehydes
  37828. allylstannanes
  37829. secondary
  37830. amine
  37831. secondary
  37832. orbital
  37833. interactions
  37834. secondary
  37835. orbital
  37836. interactions
  37837. dipolar
  37838. cycloadditions
  37839. seebach
  37840. seebach
  37841. method
  37842. seebach
  37843. review
  37844. nitro
  37845. conversion
  37846. synthesis
  37847. seebach
  37848. review
  37849. nitro
  37850. methodology
  37851. umpolung
  37852. synthesis
  37853. alkene
  37854. seebach
  37855. review
  37856. umpolung
  37857. synthesis
  37858. reagent
  37859. methodology
  37860. silico
  37861. seebach
  37862. umpolung
  37863. sulfur
  37864. carbanion
  37865. alkylation
  37866. review
  37867. seedlings
  37868. seeman
  37869. seeman
  37870. review
  37871. theory
  37872. physical
  37873. organic
  37874. curtin
  37875. hammett
  37876. hammett
  37877. seiridium
  37878. selective
  37879. selective
  37880. bromination
  37881. alpha
  37882. enones
  37883. phenyltrimethylammon
  37884. selective
  37885. oxidation
  37886. selective
  37887. reduction
  37888. selective
  37889. substitution
  37890. activated
  37891. bleomycin
  37892. carbohydrate
  37893. selective
  37894. syntheses
  37895. acrylic
  37896. compounds
  37897. derivatives
  37898. selectivities
  37899. selectivity
  37900. selectivity/chiral
  37901. selenadiazoles
  37902. selenadiazolines
  37903. selenadiazolothiadia
  37904. selenatellurolanes
  37905. selenatelluroles
  37906. selenation
  37907. selenatriazoles
  37908. selenazoles
  37909. selenazoles
  37910. selenazolines
  37911. selenazolidines
  37912. selenadiazoles
  37913. selenazolidines
  37914. selenazolines
  37915. selenide
  37916. selenide
  37917. radical
  37918. sugar
  37919. cyclization
  37920. epimerization
  37921. oxyally
  37922. selenides
  37923. selenium
  37924. selenium
  37925. chemistry
  37926. selenium
  37927. closure
  37928. selenium
  37929. oxide
  37930. oxidation
  37931. ethers
  37932. hexahydro
  37933. imino
  37934. benzazo
  37935. selenium
  37936. radical
  37937. imine
  37938. hydrazone
  37939. cyclization
  37940. nitrogen
  37941. selenium
  37942. seleno
  37943. selenoacetals
  37944. selenocarbonate
  37945. selenocarbonyl
  37946. selenolopyridazines
  37947. selenolopyridines
  37948. selenoloselen
  37949. selenols
  37950. selenophenes
  37951. selenosulfonation
  37952. selenothophenes
  37953. selenoxide
  37954. selenoxide
  37955. elimination
  37956. selenoxides
  37957. directed
  37958. semibullvallene
  37959. semicorrin
  37960. semicorrin
  37961. metal
  37962. complexes
  37963. semihydrogenation
  37964. semmler
  37965. semmler
  37966. wolff
  37967. aromatization
  37968. semones
  37969. senecio
  37970. sensitive
  37971. sensitive
  37972. sodium
  37973. channels
  37974. brain
  37975. synaptosomes
  37976. sensitization
  37977. sensitized
  37978. sensitizer
  37979. separation
  37980. sequence
  37981. sequenes
  37982. sequential
  37983. sequential
  37984. michael
  37985. additions
  37986. polycyclic
  37987. compounds
  37988. michael
  37989. sesbanimide
  37990. sesquinorbornatriene
  37991. sesquiterpene
  37992. sesquiterpenes
  37993. sesquiterpenes
  37994. cyclobutanes
  37995. pheromone
  37996. shale
  37997. shannon
  37998. shannon
  37999. review
  38000. synthesis
  38001. target
  38002. skeleton
  38003. carbazole
  38004. indole
  38005. shapiro
  38006. shapiro
  38007. reaction
  38008. sharplessE
  38009. sharpless
  38010. reaction
  38011. sharpless
  38012. asymmetric
  38013. sharpless
  38014. asymmetric
  38015. dihydroxylation
  38016. sharpless
  38017. asymmetric
  38018. epoxidation
  38019. cycloalkene
  38020. strain
  38021. bredt
  38022. theory
  38023. diels
  38024. alder
  38025. review
  38026. diels
  38027. alder
  38028. enantioselectivity
  38029. review
  38030. introduction
  38031. sheep
  38032. shibata
  38033. shibata
  38034. shift
  38035. shifts
  38036. shikimate
  38037. shikimi
  38038. shikimic
  38039. shinjulactone
  38040. shinjulactone
  38041. shono
  38042. shono
  38043. oxidation
  38044. amine
  38045. electrochem
  38046. review
  38047. electrolysis
  38048. kolbe
  38049. shono
  38050. review
  38051. electrochem
  38052. alkaloid
  38053. synthesis
  38054. electrolysis
  38055. short
  38056. allylsilanes
  38057. c-c-sir3
  38058. sialic
  38059. sialidase
  38060. review
  38061. methoxy
  38062. methylamides
  38063. acylation
  38064. carbanion
  38065. sical
  38066. sides
  38067. sievers
  38068. sievers
  38069. spectroscopy
  38070. reagent
  38071. physical
  38072. organic
  38073. shift
  38074. sigma
  38075. sigmatraopic
  38076. sigmatropic
  38077. sigmatropic
  38078. rearrangement
  38079. allylic
  38080. sulfoxide
  38081. stereochem
  38082. sigmatropic
  38083. reaction
  38084. sigmatropic
  38085. amino
  38086. ketone
  38087. oxime
  38088. nitrone
  38089. rearrangement
  38090. sigmatropic
  38091. rearrangement
  38092. sigmatropic
  38093. rearrangements
  38094. signal
  38095. signal
  38096. transduction
  38097. silacyclohexanes
  38098. silacyclohexenes
  38099. silacyclopentanes
  38100. silacyclopentenes
  38101. silacyclopropanes
  38102. silacyclopropanes
  38103. siliranes
  38104. silacyclopropenes
  38105. silirenes
  38106. silacyclopropenes
  38107. silafunctional
  38108. silane
  38109. silane
  38110. vinyloxirane
  38111. acetal
  38112. allylation
  38113. allylsilane
  38114. reagents
  38115. silanes
  38116. silanol
  38117. silatranes
  38118. silica
  38119. silica
  38120. silica
  38121. silical
  38122. silical
  38123. silicate
  38124. silicon
  38125. silicon
  38126. silicon
  38127. compounds
  38128. tetramesityldisilene
  38129. photolysis
  38130. silicon
  38131. counterattack
  38132. displacement
  38133. silicon
  38134. hydride
  38135. silicon
  38136. protecting
  38137. group
  38138. silicon
  38139. tether
  38140. silicon
  38141. tethered
  38142. silicon
  38143. tethered
  38144. diels-alder
  38145. silicon
  38146. tethered
  38147. photocyclization
  38148. silicone
  38149. silicone
  38150. silane
  38151. allyl
  38152. addition
  38153. carbonyl
  38154. fluoride
  38155. desilylatio
  38156. siliranes
  38157. silirenes
  38158. silocyclopropanes
  38159. siloles
  38160. siloxane
  38161. siloxy
  38162. siloxyacetylene
  38163. siloxycyclopropanes
  38164. siloxyfuran
  38165. siloxyfuran
  38166. diels-alder
  38167. siloxyl
  38168. silver
  38169. silver
  38170. catalyzed
  38171. cyclization
  38172. silver
  38173. catalyzed
  38174. silver
  38175. nitrate
  38176. silver
  38177. perchlorate
  38178. silver
  38179. triflate
  38180. silyl
  38181. baeyer
  38182. villiger
  38183. oxidation
  38184. silyl
  38185. baeyer-villiger
  38186. silyl
  38187. carbonyl
  38188. compounds
  38189. synthesis
  38190. enantioselective
  38191. silyl
  38192. cuprate
  38193. silyl
  38194. cyanation
  38195. silyl
  38196. deprotection
  38197. dienes
  38198. wittig
  38199. reactions
  38200. peterson
  38201. reactione
  38202. vinyl
  38203. halid
  38204. silyl
  38205. ether
  38206. silyl
  38207. ether
  38208. aldol
  38209. condensation
  38210. silyl
  38211. ether
  38212. stereochem
  38213. manganese
  38214. stereospecific
  38215. silicon
  38216. silyl
  38217. ethers
  38218. silyl
  38219. ethers
  38220. coordinated
  38221. triflate
  38222. chiral
  38223. promote
  38224. silyl
  38225. ethers
  38226. efficient
  38227. acetals
  38228. reduction
  38229. chloride
  38230. silyl
  38231. ethers
  38232. induced
  38233. enlargement
  38234. pressure
  38235. silyl
  38236. ethers
  38237. masked
  38238. michael
  38239. reaction
  38240. ethylthioketene
  38241. silyl
  38242. eonol
  38243. ether
  38244. silyl
  38245. epoxide
  38246. silyl
  38247. epoxide
  38248. azide
  38249. opening
  38250. elimination
  38251. vinyl
  38252. review
  38253. silyl
  38254. ether
  38255. silyl
  38256. ketene
  38257. acetal
  38258. silyl
  38259. ketene
  38260. acetals
  38261. silyl
  38262. ketene
  38263. acetals
  38264. mediated
  38265. reactions
  38266. simple
  38267. diastere
  38268. silyl
  38269. lithium
  38270. silane
  38271. silyl
  38272. migration
  38273. silyl
  38274. oxidation
  38275. silyl
  38276. rearrangement
  38277. silyl
  38278. sulfonyl
  38279. phenylsulfonyl
  38280. reduction
  38281. diene
  38282. diels
  38283. alder
  38284. silylamines
  38285. silylated
  38286. silylated
  38287. carbon
  38288. nucleophiles
  38289. aldol
  38290. reaction
  38291. acetals
  38292. silylation
  38293. silylative
  38294. silylcarbonylation
  38295. silylcuprate
  38296. silylcyanation
  38297. silylformylation
  38298. silylimines
  38299. silylmethyl
  38300. silyloxypyrrole
  38301. silylsilicates
  38302. simchen
  38303. review
  38304. silicon
  38305. synthesis
  38306. triflate
  38307. methodology
  38308. simmons
  38309. simmons
  38310. smith
  38311. cyclopropanation
  38312. cyclopropane
  38313. review
  38314. simmons-smith
  38315. simon
  38316. simonova
  38317. simonova
  38318. nitrenium
  38319. review
  38320. simpkins
  38321. simple
  38322. simple
  38323. enols
  38324. simulations
  38325. simultaneous
  38326. singer
  38327. singer
  38328. radical
  38329. stereochem
  38330. vinyl
  38331. review
  38332. single
  38333. single
  38334. single
  38335. electron
  38336. transfer
  38337. single
  38338. electron
  38339. transfer
  38340. enantioselective
  38341. synthesis
  38342. single
  38343. electron
  38344. transfer
  38345. triphenylmethyl
  38346. halides
  38347. photolysis
  38348. singlet
  38349. singlet
  38350. oxygen
  38351. singlet
  38352. pentafluorophenyl
  38353. nitrene
  38354. perfluorophenyl
  38355. azides
  38356. sinnott
  38357. sites
  38358. sized
  38359. skarzewski
  38360. skeletal
  38361. skeleton
  38362. skell
  38363. skell
  38364. bromination
  38365. radical
  38366. bromide
  38367. mechanism
  38368. physical
  38369. organic
  38370. slaframine
  38371. ketyl
  38372. radical
  38373. smadja
  38374. smadja
  38375. review
  38376. radical
  38377. stereochem
  38378. diastereoselective
  38379. felkin
  38380. smadja
  38381. radical
  38382. stereocenter
  38383. asymetric
  38384. diastereofacial
  38385. small
  38386. reduction
  38387. reduction
  38388. smiles
  38389. smith
  38390. smith
  38391. epoxide
  38392. review
  38393. synthesis
  38394. methodology
  38395. reduction
  38396. smith
  38397. review
  38398. diazo
  38399. ketone
  38400. alkene
  38401. cyclization
  38402. catalyst
  38403. smolin
  38404. smolin
  38405. amine
  38406. preparation
  38407. imine
  38408. review
  38409. formaldehyde
  38410. triazine
  38411. nbu3snf
  38412. sn-li
  38413. alkylation
  38414. displacement
  38415. transition
  38416. states
  38417. abinitio
  38418. nider
  38419. snider
  38420. lewis
  38421. enone
  38422. aluminum
  38423. acrylate
  38424. ester
  38425. review
  38426. snider
  38427. mechanism
  38428. stereochem
  38429. regiochem
  38430. catalyst
  38431. lewis
  38432. snider
  38433. reaction
  38434. mechanism
  38435. review
  38436. isotope
  38437. deuterium
  38438. lewis
  38439. snieckus
  38440. sulfur
  38441. dioxide
  38442. extrusion
  38443. addition
  38444. quinodimethane
  38445. rearr
  38446. so2cf3
  38447. socl2
  38448. sodium
  38449. iodide
  38450. sodium
  38451. borohydride
  38452. sodium
  38453. borohydride
  38454. paniculatine
  38455. trimethylsilyl
  38456. sodium
  38457. borohydride
  38458. reduction
  38459. sodium
  38460. borohydride
  38461. reduction
  38462. reducing
  38463. agent
  38464. aqueous
  38465. sodium
  38466. chlorite
  38467. sodium
  38468. cyanoborohydride
  38469. sodium
  38470. hydrogen
  38471. telluride
  38472. sodium
  38473. reduction
  38474. sodium
  38475. triacetoxyborohydrid
  38476. solenopsin
  38477. solid
  38478. solid
  38479. phase
  38480. carbohydrate
  38481. synthesis
  38482. solid
  38483. phase
  38484. carbohydrate
  38485. synthesis
  38486. solid
  38487. phase
  38488. peptide
  38489. synthesis
  38490. solid
  38491. phase
  38492. reaction
  38493. surface
  38494. mediated
  38495. reactions
  38496. solid
  38497. phase
  38498. synthesis
  38499. peptide
  38500. synthesis
  38501. deprotection
  38502. phospha
  38503. solid
  38504. state
  38505. polymerization
  38506. electron
  38507. resonance
  38508. singlet
  38509. solid
  38510. state
  38511. polymerization
  38512. polyynes
  38513. diacetylenes
  38514. 660631
  38515. solids
  38516. solladie
  38517. sollhuber
  38518. sollhuber
  38519. ultrasound
  38520. review
  38521. reference
  38522. strecker
  38523. cyano
  38524. amine
  38525. solution
  38526. solutions
  38527. solvating
  38528. solvation
  38529. solvent
  38530. solvents
  38531. solvolysis
  38532. sonication
  38533. sonnet
  38534. sonnet
  38535. inversion
  38536. alkene
  38537. isomerization
  38538. equilibration
  38539. stereoch
  38540. sonochemistry
  38541. sound
  38542. space
  38543. spangler
  38544. spangler
  38545. sigmatropic
  38546. rearrangement
  38547. thermal
  38548. review
  38549. orbital
  38550. sparteine
  38551. species
  38552. specificity
  38553. speckamp
  38554. speckamp
  38555. azomethine
  38556. ylide
  38557. review
  38558. electrocyclization
  38559. electroc
  38560. speckamp
  38561. review
  38562. radical
  38563. iminium
  38564. spectra
  38565. spectrometry
  38566. spectroscopic
  38567. spectroscopic
  38568. detection
  38569. additions
  38570. arylaminothio
  38571. spectroscopy
  38572. spectrum
  38573. spengler
  38574. sphere
  38575. sphinganine
  38576. sphingosine
  38577. spiro
  38578. spiroacetals
  38579. spiroamine
  38580. spiroannelation
  38581. spiroannulation
  38582. spiroconjugation
  38583. spiroconjugation
  38584. cyclopropene
  38585. cyclopentadiene
  38586. spirotriene
  38587. spirocycle
  38588. spirocycles
  38589. spirocyclic
  38590. spirocyclisation
  38591. spirocyclization
  38592. spirocyclopropane
  38593. spirodienones
  38594. spiroketal
  38595. spiroketal
  38596. formation
  38597. spiroketal
  38598. fragment
  38599. glycopeptides
  38600. carbomycin
  38601. allylstanna
  38602. spiroketals
  38603. spirooxindoles
  38604. spiropentadiene
  38605. spirotriene
  38606. sponge
  38607. sponge
  38608. discodermia
  38609. calyx
  38610. calyculin
  38611. stereocontrolled
  38612. synthe
  38613. sponge
  38614. theonella
  38615. peptidyl
  38616. fluoromethyl
  38617. ketones
  38618. bioactive
  38619. spray
  38620. squarate
  38621. reaction
  38622. stability
  38623. stability
  38624. captodative
  38625. effect
  38626. stabilization
  38627. stabilized
  38628. stable
  38629. stable
  38630. derivatives
  38631. photochemistry
  38632. stang
  38633. stang
  38634. alkene
  38635. vinyl
  38636. cation
  38637. triflate
  38638. review
  38639. rearrangement
  38640. stang
  38641. carbene
  38642. review
  38643. alkene
  38644. vinyl
  38645. addition
  38646. triflate
  38647. methodol
  38648. stang
  38649. triflate
  38650. triflic
  38651. fluorine
  38652. sulfonyl
  38653. reaction
  38654. review
  38655. stang
  38656. triflate
  38657. vinyl
  38658. synthesis
  38659. triflic
  38660. anhydride
  38661. review
  38662. stannacyclopentanes
  38663. stannane
  38664. stannane
  38665. alpha
  38666. alkoxy
  38667. amino
  38668. palladium
  38669. cross
  38670. coupling
  38671. stannanes
  38672. stannes
  38673. stannic
  38674. stannic
  38675. chloride
  38676. stannoles
  38677. stannyl
  38678. stannyl
  38679. cuprate
  38680. addition
  38681. stannylation
  38682. stannylcupration
  38683. stannylhydrin
  38684. stannylhydrin
  38685. chiral
  38686. induction
  38687. trimethyl
  38688. tributylstannyl
  38689. stannylimidoyl
  38690. stanounik
  38691. stanounik
  38692. diazo
  38693. heteroaromatic
  38694. review
  38695. dipole
  38696. dipolar
  38697. cycload
  38698. stanovnik
  38699. stanovnik
  38700. dipolar
  38701. cycloaddition
  38702. review
  38703. nitrogen
  38704. heterocycle
  38705. state
  38706. state
  38707. staudinger
  38708. stegelmeier
  38709. stegelmeier
  38710. azepine
  38711. synthesis
  38712. spectroscopy
  38713. substitution
  38714. steinmetz
  38715. steinmetz
  38716. review
  38717. cyclopropene
  38718. allene
  38719. vinyl
  38720. carbene
  38721. photochem
  38722. stella
  38723. stella
  38724. amine
  38725. chloro
  38726. radical
  38727. addition
  38728. review
  38729. cyclization
  38730. stella
  38731. intramolecular
  38732. cyclization
  38733. radical
  38734. cation
  38735. review
  38736. stephenson
  38737. stephenson
  38738. mechanism
  38739. isotope
  38740. effect
  38741. stereochem
  38742. regiochem
  38743. stepwise
  38744. stere
  38745. stereo
  38746. stereocenter
  38747. stereochemI
  38748. stereochem
  38749. dipolar
  38750. cycloaddition
  38751. nitrile
  38752. oxide
  38753. nitrone
  38754. revie
  38755. stereochemi
  38756. stereochemical
  38757. stereochemical
  38758. aspects
  38759. organic
  38760. synthesis
  38761. stereochemical
  38762. control
  38763. stereochemical
  38764. control
  38765. quinones
  38766. diene
  38767. stereochemis
  38768. stereochemist
  38769. stereochemistr
  38770. stereochemistry
  38771. stereochemistry
  38772. stereochemistry
  38773. rearrangement
  38774. alkenes
  38775. stereocontrol
  38776. stereocontrolled
  38777. stereocontrolled
  38778. lactonization
  38779. reactions
  38780. conjugated
  38781. dienes
  38782. stereocontrolled
  38783. lactonization
  38784. reactions
  38785. palladium
  38786. catalyzed
  38787. stereocontrolled
  38788. synthesis
  38789. stereocontrolled
  38790. synthesis
  38791. carbapenem
  38792. antibiotics
  38793. precursors
  38794. stereocontrolled
  38795. synthesis
  38796. dipeptide
  38797. isosteres
  38798. protease
  38799. stereodifferentiatio
  38800. oelectronic
  38801. stereoelectronics
  38802. stereogenic
  38803. stereoinduction
  38804. stereoisomer
  38805. stereoisomers
  38806. stereoselection
  38807. stereoselective
  38808. stereoselective
  38809. stereoselective
  38810. cuprate
  38811. addition
  38812. stereoselective
  38813. formation
  38814. cyclic
  38815. ethers
  38816. tetrahydropyrans
  38817. stereoselective
  38818. preparation
  38819. neopentylidene
  38820. complexes
  38821. stereoselective
  38822. reduction
  38823. stereoselective
  38824. reduction
  38825. ketone
  38826. stereoselective
  38827. synthesis
  38828. asymmetric
  38829. synthesis
  38830. reduction
  38831. stereoselective
  38832. synthesis
  38833. condensations
  38834. acids
  38835. stereoselective
  38836. synthesis
  38837. derivatives
  38838. taxane
  38839. stereoselective
  38840. total
  38841. synthesis
  38842. stereoselectivity
  38843. stereospecific
  38844. stereospecific
  38845. stereospecific
  38846. elimination
  38847. stereospecific
  38848. group
  38849. transfer
  38850. hydride
  38851. capture
  38852. cascade
  38853. stereospecific
  38854. hydrohalogenation
  38855. reaction
  38856. catalyzed
  38857. stereose
  38858. stereospecific
  38859. synthesis
  38860. stereoselectivity
  38861. cycloaddition
  38862. stereospecific
  38863. total
  38864. synthesis
  38865. formal
  38866. total
  38867. synthesis
  38868. alkyll
  38869. steric
  38870. steric
  38871. control
  38872. sterically
  38873. sterically
  38874. congested
  38875. molecules
  38876. steriod
  38877. steriod
  38878. biosynthesis
  38879. steroid
  38880. chains
  38881. steroid
  38882. skeleton
  38883. steroids
  38884. stevens
  38885. stevens
  38886. rearrangement
  38887. stewart
  38888. stewart
  38889. sydnone
  38890. review
  38891. mesoionic
  38892. cycloaddition
  38893. extrusion
  38894. stibolanes
  38895. stiboles
  38896. stiegli
  38897. stilbene
  38898. stilbene
  38899. deriv
  38900. activity
  38901. synthesis
  38902. stilbene
  38903. compounds
  38904. photodehydrocyclizat
  38905. helicenes
  38906. stilbenes
  38907. stille
  38908. stille
  38909. coupling
  38910. catalyzed
  38911. coupling
  38912. stille
  38913. reaction
  38914. stille
  38915. review
  38916. coupling
  38917. catalyzed
  38918. palladium
  38919. electrophile
  38920. stobbe
  38921. stoddart
  38922. stoddart
  38923. synthesis
  38924. cyclodextrin
  38925. review
  38926. stoichiometric
  38927. stork
  38928. stork
  38929. review
  38930. radical
  38931. cyclization
  38932. intramolecular
  38933. addition
  38934. stork
  38935. takahashi
  38936. alkylation
  38937. stowell
  38938. stowell
  38939. review
  38940. carbon
  38941. three
  38942. homologation
  38943. reagent
  38944. enone
  38945. exten
  38946. strain
  38947. strained
  38948. strategies
  38949. strategy
  38950. strecker
  38951. streith
  38952. streith
  38953. hetero
  38954. hydroxyl
  38955. amine
  38956. cleavage
  38957. nitrogen
  38958. oxygen
  38959. strengths
  38960. streptomyces
  38961. streptonigrin
  38962. stretching
  38963. stretching
  38964. frequencies
  38965. transition
  38966. metal
  38967. complexes
  38968. strontium
  38969. structural
  38970. structural
  38971. studies
  38972. structurally
  38973. structurally
  38974. related
  38975. compounds
  38976. active
  38977. natural
  38978. carotenoids
  38979. structurally
  38980. simple
  38981. butenolides
  38982. spiroketals
  38983. rearrangemen
  38984. structure
  38985. structures
  38986. strychnos
  38987. strychnos
  38988. alkaloids
  38989. strychnos
  38990. alkaloids
  38991. indole
  38992. alkaloids
  38993. entry
  38994. strychnos
  38995. indole
  38996. alkaloids
  38997. modified
  38998. polonovski
  38999. reaction
  39000. student
  39001. studies
  39002. study
  39003. suboxide
  39004. subrahanyam
  39005. subrahanyam
  39006. isoxazole
  39007. methodology
  39008. review
  39009. heterocycle
  39010. cycload
  39011. subsitution
  39012. substance
  39013. substitu
  39014. substituent
  39015. substituents
  39016. substituents/cyclo-a
  39017. substituents/multich
  39018. substituted
  39019. substituted
  39020. halides
  39021. stereoselective
  39022. synthesis
  39023. nitrogen
  39024. substituted
  39025. cyclobutenediones
  39026. calicheamicin
  39027. substituted
  39028. cyclopentane
  39029. derivatives/dithioes
  39030. substituted
  39031. furans
  39032. cyclo
  39033. additions
  39034. derivatives
  39035. annelation
  39036. substituted
  39037. organolithium
  39038. compounds
  39039. temperature
  39040. substituted
  39041. pyridines
  39042. methoxycarbonyl
  39043. group
  39044. iodide
  39045. demethyla
  39046. substituted
  39047. tetrahydrofurans
  39048. captodative
  39049. stabilization
  39050. radic
  39051. substituted
  39052. vinylcyclopropanes
  39053. radical
  39054. annulation
  39055. reagents
  39056. substitution
  39057. subrahanyam
  39058. isoxazole
  39059. methodology
  39060. review
  39061. heterocycle
  39062. cycload@
  39063. substitution
  39064. substitution
  39065. ph2nch2sph
  39066. tbuli
  39067. ph2nch2tbu
  39068. ph2nch
  39069. sulfenamide
  39070. sulfinimide@
  39071. sulfone
  39072. sulfoxides@
  39073. super
  39074. hydride@
  39075. supinidine
  39076. suzuki
  39077. boron
  39078. review
  39079. alkene
  39080. alkyne
  39081. synthesis
  39082. organometallic
  39083. reactivity
  39084. ethers@
  39085. t-butyl@
  39086. tandem
  39087. anionic
  39088. cyclization
  39089. radical
  39090. chain
  39091. reactions
  39092. organic
  39093. target
  39094. target
  39095. synthesis
  39096. macrolides
  39097. spiroacetals
  39098. avermectins
  39099. milbemy
  39100. target
  39101. synthesis
  39102. pheromones@
  39103. tartarate
  39104. chiral
  39105. auxiliary@
  39106. terminated@
  39107. tetrachloromethane
  39108. tetrazines
  39109. pentazines@
  39110. thebtararonth
  39111. review
  39112. cationic
  39113. radical
  39114. anionic
  39115. metal
  39116. thiaannulenes@
  39117. thiazolopyridazines@
  39118. review
  39119. alkylation
  39120. enamide
  39121. spectroscopy
  39122. sulfur
  39123. thioa@
  39124. thioimide@
  39125. removal@
  39126. titanacycle
  39127. lines
  39128. ammelides
  39129. acetog@
  39130. substitution
  39131. ph2nch2sph
  39132. tbuli
  39133. ph2nch2tbu
  39134. ph2nch
  39135. substitution
  39136. reagents
  39137. ketones
  39138. substitutions
  39139. substrate
  39140. substructure
  39141. subunit
  39142. succinimide
  39143. sufoxide
  39144. sufoxide
  39145. dienophile
  39146. sugar
  39147. sugar
  39148. chemistry
  39149. sugars
  39150. sugars/chiral
  39151. sukumaran
  39152. sukumaran
  39153. photocycloaddition
  39154. heterocycle
  39155. diels
  39156. alder
  39157. cycliza
  39158. sulfamyl
  39159. sulfate
  39160. sulfates
  39161. sulfde
  39162. sulfenamide
  39163. sulfenamide
  39164. sulfenamines
  39165. sulfenate
  39166. sulfene
  39167. sulfenyl
  39168. sulfenylation
  39169. sulfide
  39170. sulfide
  39171. oxidation
  39172. sulfide
  39173. oxidation
  39174. sulfone
  39175. review
  39176. reagent
  39177. experimental
  39178. osmium
  39179. sulfide
  39180. sulfone
  39181. experimental
  39182. reagent
  39183. oxidation
  39184. ruthenium
  39185. sulfides
  39186. sulfil
  39187. sulfilimides
  39188. sulfilimines
  39189. sulfinamides
  39190. sulfinate
  39191. inimide
  39192. sulfinimines
  39193. sulfinyl
  39194. sulfite
  39195. sulfites
  39196. sulfolenes
  39197. sulfonamide
  39198. sulfonamides
  39199. sulfonamides
  39200. acids
  39201. sulfonated
  39202. sulfone
  39203. sulfone
  39204. sulfone
  39205. anion
  39206. sulfone
  39207. carbanion
  39208. sulfone
  39209. carbanion
  39210. ester
  39211. addition
  39212. cyclization
  39213. target
  39214. nickel
  39215. sulfone
  39216. carbanion
  39217. sulfones
  39218. sulfonic
  39219. sulfonic
  39220. carboxylic
  39221. anhydrides
  39222. ammonium
  39223. nitrate
  39224. epoxide
  39225. sulfonium
  39226. sulfonium
  39227. ylide
  39228. displacement
  39229. halide
  39230. alkene
  39231. elimination
  39232. vinyl
  39233. sulfonyl
  39234. sulfonyl
  39235. anions
  39236. sulfonylated
  39237. sulfonylated
  39238. hydroxamic
  39239. acids
  39240. sulfonylated
  39241. hydroxamic
  39242. acids
  39243. enantioselective
  39244. synthesis
  39245. sulfonylimines
  39246. sulfoxide
  39247. sulfoxides
  39248. sulfoximides
  39249. sulfoximine
  39250. sulfoximines
  39251. sulfoxonium
  39252. sulfoxyl
  39253. sulfur
  39254. sulfur
  39255. carbanions
  39256. sulfur
  39257. chemistry
  39258. sulfur
  39259. chemistry
  39260. allium
  39261. sulfur
  39262. silicon
  39263. chemistry
  39264. sulfur
  39265. stabilized
  39266. carbanion
  39267. sulfur
  39268. ylide
  39269. sulfur
  39270. ylide
  39271. rhodium
  39272. diazo
  39273. ester
  39274. aldehyde
  39275. epoxide
  39276. preparatio
  39277. sulfuranes
  39278. sulphenic
  39279. sulphenylation
  39280. sulphides
  39281. sulphones
  39282. sulphonyl
  39283. sulphoxides
  39284. sulphur
  39285. sultam
  39286. sultine
  39287. sultones
  39288. super
  39289. hydride
  39290. superacidic
  39291. superbases
  39292. superoxide
  39293. supinidine
  39294. supinidine
  39295. support
  39296. supporte
  39297. supported
  39298. supports
  39299. surface
  39300. surface
  39301. nature
  39302. electron
  39303. transfer
  39304. mechanism
  39305. magnesium
  39306. reactiv
  39307. survey
  39308. sustman
  39309. sustmann
  39310. sustmann
  39311. review
  39312. introduction
  39313. diels
  39314. alder
  39315. failure
  39316. suzuki
  39317. review
  39318. alkene
  39319. alkyne
  39320. synthesis
  39321. organometallic
  39322. suzuki
  39323. coupling
  39324. swainsona
  39325. swainsonine
  39326. switch
  39327. switches
  39328. sydnone
  39329. sydnone
  39330. compounds
  39331. schmidt
  39332. reaction
  39333. symmetrical
  39334. symmetry
  39335. addition
  39336. aldol
  39337. aldol
  39338. reaction
  39339. cyclopropanation
  39340. selectivity
  39341. baeyer
  39342. villiger
  39343. synaptosomes
  39344. synchronization
  39345. synclinal
  39346. syndiotactic
  39347. synlettF
  39348. synthase
  39349. synthes
  39350. synthes
  39351. syntheses
  39352. synthesis
  39353. synthesis
  39354. synthesis
  39355. synthesis
  39356. synthesis
  39357. shikimi
  39358. synthesis
  39359. oxaziridine
  39360. review
  39361. lactam
  39362. heterocycle
  39363. annulat
  39364. synthesis
  39365. reference
  39366. writing
  39367. dipole
  39368. dipolar
  39369. cycloaddition
  39370. synthesis
  39371. review
  39372. alkaloid
  39373. amine
  39374. methoxy
  39375. cation
  39376. radical
  39377. elect
  39378. synthesis
  39379. review
  39380. carbanion
  39381. vinyl
  39382. addition
  39383. amine
  39384. alkyne
  39385. carba
  39386. synthetic
  39387. synthetic
  39388. lications
  39389. dienes
  39390. reactivity
  39391. amines
  39392. synthetic
  39393. roach
  39394. system
  39395. synthetic
  39396. applications
  39397. malonate
  39398. esters
  39399. synthetic
  39400. applications
  39401. stannyl
  39402. cupration
  39403. synthetic
  39404. auxiliary
  39405. salts
  39406. heterocycles
  39407. reactivity
  39408. ethers
  39409. synthetic
  39410. equivalents
  39411. aminoorganolithiums
  39412. reagents
  39413. synthetic
  39414. equivalents
  39415. nuclear
  39416. magnetic
  39417. resonance
  39418. synthetic
  39419. methods
  39420. synthetic
  39421. routes
  39422. cyclizations
  39423. synthetic
  39424. utility
  39425. synthon
  39426. synthons
  39427. system
  39428. kynylcyclobutenone
  39429. calichemicin
  39430. chemistry
  39431. systems
  39432. szabo
  39433. szabo
  39434. review
  39435. isocyanate
  39436. reagent
  39437. chloro
  39438. sulfonyl
  39439. dougherty
  39440. cancer
  39441. photochemistry
  39442. review
  39443. mitchell
  39444. stille
  39445. coupling
  39446. palladium
  39447. stannane
  39448. alkene
  39449. t-buok
  39450. t-buooh
  39451. t-butoxide
  39452. t-butyl
  39453. t-butyl
  39454. ester
  39455. t-butyl
  39456. hydroperoxide
  39457. t-butyldimethylsilyl
  39458. t-butyldimethylsilyl
  39459. ether
  39460. t-butyldiphenylsilyl
  39461. t-butyldiphenylsilyl
  39462. ether
  39463. t-butylhydroperoxide
  39464. tabersonine
  39465. takahashi
  39466. takahata
  39467. takahata
  39468. heterocyclic
  39469. thioamide
  39470. sulfur
  39471. synthesis
  39472. review
  39473. takahata
  39474. thioamide
  39475. review
  39476. heterocycle
  39477. method
  39478. synthesis
  39479. takai
  39480. takai
  39481. nozaki
  39482. reaction
  39483. vinyl
  39484. iodide
  39485. synthesis
  39486. takeuchi
  39487. takeuchi
  39488. wittig
  39489. reaction
  39490. stereoselectivity
  39491. phosphorous
  39492. ylide
  39493. talley
  39494. talley
  39495. quinone
  39496. ortho
  39497. methide
  39498. intramolecular
  39499. diels
  39500. alder
  39501. tallics
  39502. tamao
  39503. tamao
  39504. oxidation
  39505. tamminen
  39506. tandem
  39507. tandem
  39508. nitroalkene
  39509. cycloaddition
  39510. tandem
  39511. alkylation
  39512. tandem
  39513. anionic
  39514. cyclization
  39515. tandem
  39516. anionic
  39517. cyclization
  39518. radical
  39519. chain
  39520. reactions
  39521. organic
  39522. tandem
  39523. cyclization
  39524. tandem
  39525. elimination
  39526. reduction
  39527. sulfone
  39528. chiral
  39529. reductive
  39530. reduct
  39531. tandem
  39532. heterocycle
  39533. beckmann
  39534. allyl
  39535. silane
  39536. cyclization
  39537. cephalo
  39538. tandem
  39539. intramolecular
  39540. diels-alder
  39541. aldol
  39542. reaction
  39543. tandem
  39544. michael
  39545. addition
  39546. aldol
  39547. reaction
  39548. tandem
  39549. michael
  39550. addition
  39551. dieckmann
  39552. condensation
  39553. cotoxin
  39554. epoxy
  39555. keton
  39556. tanshinones
  39557. tantalum
  39558. target
  39559. target
  39560. target
  39561. synthes
  39562. antibiotics
  39563. target
  39564. synthesis
  39565. target
  39566. synthesis
  39567. alkaloids
  39568. heterocycles
  39569. lactim
  39570. ether
  39571. target
  39572. synthesis
  39573. alkaloids
  39574. heterocycles
  39575. n-alkylpyridinium
  39576. target
  39577. synthesis
  39578. alkaloids
  39579. pschorr
  39580. photocyclisation
  39581. phenol
  39582. target
  39583. synthesis
  39584. indolizidine
  39585. alkaloids
  39586. target
  39587. synthesis
  39588. ivermectin
  39589. target
  39590. synthesis
  39591. leukotrienes
  39592. formation
  39593. target
  39594. synthesis
  39595. leukotrienes
  39596. prostaglandins
  39597. target
  39598. synthesis
  39599. macrolides
  39600. target
  39601. synthesis
  39602. macrolides
  39603. formation
  39604. heteroannulat
  39605. target
  39606. synthesis
  39607. macrolides
  39608. formation
  39609. annulations
  39610. target
  39611. synthesis
  39612. macrolides
  39613. ionophores
  39614. target
  39615. synthesis
  39616. macrolides
  39617. macrolides
  39618. natural
  39619. oducts
  39620. target
  39621. synthesis
  39622. macrolides
  39623. natural
  39624. products
  39625. target
  39626. synthesis
  39627. macrolides
  39628. natural
  39629. products
  39630. antibiotics
  39631. target
  39632. synthesis
  39633. macrolides
  39634. spiroacetals
  39635. avermectins
  39636. milbemy
  39637. target
  39638. synthesis
  39639. macrolides
  39640. spiroacetals
  39641. avermectins
  39642. milbemy
  39643. target
  39644. synthesis
  39645. marine
  39646. natural
  39647. products
  39648. target
  39649. synthesis
  39650. miscellaneous
  39651. target
  39652. synthesis
  39653. miscellaneous
  39654. anthracyclinones
  39655. target
  39656. synthesis
  39657. miscellaneous
  39658. arenes
  39659. target
  39660. synthesis
  39661. miscellaneous
  39662. biotransformation
  39663. enzyme
  39664. target
  39665. synthesis
  39666. miscellaneous
  39667. functional
  39668. groups
  39669. protection
  39670. target
  39671. synthesis
  39672. miscellaneous
  39673. heterocycles
  39674. lactams
  39675. heterocy
  39676. target
  39677. synthesis
  39678. miscellaneous
  39679. hetring
  39680. nitril
  39681. target
  39682. synthesis
  39683. miscellaneous
  39684. indole
  39685. alkaloids
  39686. target
  39687. synthesis
  39688. miscellaneous
  39689. lactams
  39690. hetring
  39691. target
  39692. synthesis
  39693. miscellaneous
  39694. nucleosides
  39695. nucleotides
  39696. nucle
  39697. target
  39698. synthesis
  39699. miscellaneous
  39700. peptides
  39701. target
  39702. synthesis
  39703. miscellaneous
  39704. reagents
  39705. peptides
  39706. target
  39707. synthesis
  39708. miscellaneous
  39709. synthon
  39710. oxazoles
  39711. heterocycles
  39712. target
  39713. synthesis
  39714. nucleosides
  39715. carbohydrates
  39716. target
  39717. synthesis
  39718. pheromone
  39719. target
  39720. synthesis
  39721. pheromones
  39722. target
  39723. synthesis
  39724. prostaglandins
  39725. leukotrienes
  39726. target
  39727. synthesis
  39728. prostaglandins
  39729. leukotrienes
  39730. prostacyclin
  39731. target
  39732. synthesis
  39733. prostaglandins
  39734. leukotrienes
  39735. prostaglandins
  39736. target
  39737. synthesis
  39738. reagents
  39739. calixarenes
  39740. target
  39741. synthesis
  39742. terpenoids
  39743. target
  39744. synthesis
  39745. terpenoids
  39746. carbring
  39747. hydroazulene
  39748. target
  39749. synthesis
  39750. terpenoids
  39751. functional
  39752. groups
  39753. preparations
  39754. target
  39755. synthesis
  39756. terpenoids
  39757. mevinic
  39758. acids
  39759. target
  39760. synthesis
  39761. terpenoids
  39762. unnatural
  39763. products
  39764. target
  39765. synthesis
  39766. total
  39767. synthesis
  39768. target
  39769. synthesis
  39770. unnatural
  39771. products
  39772. target
  39773. synthesis
  39774. unnatural
  39775. products
  39776. 2-arylpropionic
  39777. acids
  39778. target
  39779. synthesis
  39780. unnatural
  39781. products
  39782. annulation
  39783. 5-ring
  39784. target
  39785. synthesis
  39786. unnatural
  39787. products
  39788. annulation
  39789. coupling
  39790. target
  39791. synthesis
  39792. unnatural
  39793. products
  39794. carbrin
  39795. target
  39796. synthesis
  39797. unnatural
  39798. products
  39799. carbring
  39800. tartarate
  39801. tartarate
  39802. chiral
  39803. auxiliary
  39804. tartarate
  39805. i-opr
  39806. tartaric
  39807. tartrate
  39808. tashner
  39809. taste
  39810. allyl
  39811. complexes
  39812. dipolar
  39813. cycloaddition
  39814. nitrile
  39815. tautomer
  39816. tautomeric
  39817. tautomerism
  39818. tautomerization
  39819. taxane
  39820. taxanes
  39821. taxinine
  39822. taxol
  39823. taxol
  39824. synthesis
  39825. taxol
  39826. atropisomerism
  39827. membered
  39828. intramolecular
  39829. cyclizat
  39830. taxol
  39831. intermediate
  39832. taxol
  39833. skeleton
  39834. system
  39835. taxols
  39836. taylor
  39837. taylor
  39838. review
  39839. synthesis
  39840. diketone
  39841. writing
  39842. experimental
  39843. taylor
  39844. review
  39845. synthesis
  39846. prostaglandin
  39847. strategy
  39848. target
  39849. natura
  39850. taylor
  39851. turchi
  39852. higher
  39853. order
  39854. cyclization
  39855. dipole
  39856. dipolar
  39857. electr
  39858. deprotection
  39859. protected
  39860. urethane
  39861. tbsotf
  39862. tbuli
  39863. tbuok
  39864. teach
  39865. teaching
  39866. tebbe
  39867. tebbe
  39868. olefination
  39869. tebbe
  39870. reaction
  39871. tebbe
  39872. reagent
  39873. techniques
  39874. methods
  39875. ultrasound
  39876. telluride
  39877. telluride
  39878. epoxide
  39879. opening
  39880. chiral
  39881. alcohol
  39882. stereochem
  39883. tellurides
  39884. tellurium
  39885. tellurium
  39886. lithium
  39887. allyl
  39888. benzyl
  39889. halide
  39890. organotellurium
  39891. chemis
  39892. tellurium
  39893. nucleophile
  39894. tellurophenes
  39895. temperature
  39896. template
  39897. template/allylic
  39898. temporary
  39899. temporary
  39900. silicon
  39901. connection
  39902. tenes
  39903. terminal
  39904. terminal
  39905. olefin
  39906. terminal
  39907. olefins
  39908. terminated
  39909. termination
  39910. terminus
  39911. terpene
  39912. terpenoids
  39913. butoxy
  39914. radicals
  39915. reactivity
  39916. butyl
  39917. bromide
  39918. tert-butyl
  39919. tert-butyl
  39920. dimethylsilyl
  39921. tert-butylperoxide
  39922. tertiary
  39923. tertiary
  39924. alcohol
  39925. synthesis
  39926. tertiary
  39927. alkyl
  39928. chlorides
  39929. tether
  39930. tetra
  39931. tetraacetate
  39932. tetraacetylethylene
  39933. tetraalkylstannanes
  39934. tetraalkylstannanes
  39935. cyclization
  39936. chemistry
  39937. complex
  39938. tetrabromide
  39939. tetrabutyl
  39940. tetrabutyl
  39941. ammonium
  39942. chloride
  39943. tetrabutyl
  39944. ammonium
  39945. fluoride
  39946. tetrabutylammonium
  39947. tetrabutylammonium
  39948. fluoride
  39949. tetracarbonylhydroco
  39950. tetracarbonyliron
  39951. tetrachloride
  39952. tetrachloromethane
  39953. tetrafluoride
  39954. tetrahalide
  39955. tetrahydofuran
  39956. tetrahydofurans
  39957. tetrahydro
  39958. tetrahydro-carboline
  39959. tetrahydroazepine
  39960. tetrahydrocarbolines
  39961. tetrahydrofuran
  39962. tetrahydrofuran
  39963. synthesis
  39964. tetrahydrofurans
  39965. tetrahydropyran
  39966. tetrahydropyran
  39967. synthesis
  39968. tetrahydropyran-4-on
  39969. tetrahydropyrans
  39970. tetrahydropyridines
  39971. tetrahydropyrone
  39972. tetrahydrothiop
  39973. ylphosphine
  39974. palladium
  39975. tetramesityldisilene
  39976. tetramethylethylenes
  39977. tetramic
  39978. tetraoxide
  39979. tetrathiepins
  39980. tetrathiocanes
  39981. tetrazenes
  39982. tetrazepines
  39983. tetrazetidines
  39984. tetrazine
  39985. tetrazines
  39986. tetrazines
  39987. pentazines
  39988. tetrazino
  39989. tetrazocanes
  39990. tetrazocines
  39991. tetrazole
  39992. tetrazole
  39993. nitrile
  39994. trimethylsilylazide
  39995. azide
  39996. trimethylal
  39997. tetrazole
  39998. metalation
  39999. tetrazoles
  40000. tetrazolines
  40001. tetrazoloisoquinolin
  40002. tetrazolopyrazines
  40003. tetrazolopyridazines
  40004. tetrazolopyridines
  40005. tetrazolopyrimidines
  40006. tetrazoloquinazoline
  40007. tetrazoloquinoxaline
  40008. tetrazolotria
  40009. tetronasin
  40010. tetroxide
  40011. tetroxocanes
  40012. teuber
  40013. protecting
  40014. group
  40015. thallium
  40016. thallium
  40017. acetate
  40018. thallium
  40019. carbonate
  40020. thallium
  40021. hydroxide
  40022. thallium
  40023. thebtaranonth
  40024. thebtaranonth
  40025. review
  40026. cyclization
  40027. reaction
  40028. cation
  40029. radical
  40030. thebtaranoth
  40031. thebtararonth
  40032. thebtararonth
  40033. review
  40034. cationic
  40035. radical
  40036. anionic
  40037. metal
  40038. their
  40039. theobromines
  40040. theonella
  40041. theophyllines
  40042. theor
  40043. theoretical
  40044. theory
  40045. theory
  40046. lithiate
  40047. carbanion
  40048. review
  40049. chemistry
  40050. structure
  40051. physica
  40052. thermal
  40053. thermal
  40054. cycloaddition
  40055. thermal
  40056. cyclization
  40057. dioxetanes
  40058. mechanisms
  40059. dibenzyl
  40060. thermal
  40061. degradation
  40062. ethenyl
  40063. cations
  40064. thermal
  40065. reaction
  40066. thermal
  40067. rearrangement
  40068. thermal
  40069. stability
  40070. thermic
  40071. thermolabile
  40072. thermolysis
  40073. thers
  40074. thexylborane
  40075. thiaannulenes
  40076. thiabenzenes
  40077. thiabutadienes
  40078. thiadiazepines
  40079. thiadiazetidines
  40080. thiadiazines
  40081. thiadiazol
  40082. thiadiazoles
  40083. thiadiazolidines
  40084. thiadiazolines
  40085. thiadiazolines
  40086. thiadiazolidines
  40087. thiadiazolopyrazines
  40088. thiadiazolopyridazin
  40089. thiadiazolopyrimidin
  40090. thiadiazolothiadiazo
  40091. thiadiselenole
  40092. thiamin
  40093. thianes
  40094. thianthrenes
  40095. thiaselenolanes
  40096. thiaselenoles
  40097. thiatellurolanes
  40098. thiatelluroles
  40099. thiatriazepines
  40100. thiatriazines
  40101. thiatriazoles
  40102. thiatriazolidines
  40103. thiatriazolines
  40104. thiatriazolines
  40105. oxatriazolines
  40106. thiatriazolidines
  40107. selenatriaz
  40108. thiazepines
  40109. thiazetidines
  40110. thiazines
  40111. thiazinones
  40112. thiazocanes
  40113. thiazole
  40114. thiazoles
  40115. thiazolidine
  40116. thiazolidines
  40117. thiazoline
  40118. thiazolines
  40119. thiazolines
  40120. thiazolidines
  40121. thiazolopyrazines
  40122. thiazolopyridazines
  40123. thiazolopyridines
  40124. thiazolopyrimidines
  40125. thiazolotriazoles
  40126. thiazolotriazoles
  40127. pyrazolothiadiazoles
  40128. thienodithiolanes
  40129. thiazolyl
  40130. thiele
  40131. thiele-winter
  40132. thienamycin
  40133. thienamycin
  40134. antibiotics
  40135. derivatives
  40136. thienamycins
  40137. thieno
  40138. thienodithiolanes
  40139. thienofurans
  40140. thienoisothiazoles
  40141. thienooxodiazoles
  40142. thienopyrazines
  40143. thienopyrazoles
  40144. thienopyridazines
  40145. thienopyridines
  40146. thienopyrimidines
  40147. thienopyrroles
  40148. thienoquinolin
  40149. thienoquinoxalines
  40150. thienotheiophenes
  40151. thienothiadiazoles
  40152. thienothiazoles
  40153. thienothiophenes
  40154. thienothiophenes
  40155. thienofurans
  40156. thienopyrroles
  40157. selenothophenes
  40158. thienotriazoles
  40159. thietanones
  40160. thietanones
  40161. a-thiolactones
  40162. thiete
  40163. thiins
  40164. thiirane
  40165. thiiranes
  40166. thiiranium
  40167. thiiranium
  40168. sulfenylation
  40169. asymmetric
  40170. sulfonium
  40171. dimethyl
  40172. methy
  40173. thioD
  40174. glycosides
  40175. enamide
  40176. spectroscopy
  40177. sulfur
  40178. thioa
  40179. sulfur
  40180. radical
  40181. cyclization
  40182. review
  40183. carbonyl
  40184. crich
  40185. thioacetal
  40186. thioacetales
  40187. thioaldehyde
  40188. thioamidates
  40189. thioamide
  40190. thioamide
  40191. preparation
  40192. review
  40193. reagent
  40194. lawessons
  40195. lawesson
  40196. thioamides
  40197. thiocanes
  40198. thiocarbamate
  40199. thiocarbonic
  40200. thiocarbonic
  40201. ester
  40202. thiocarbonyl
  40203. thiocarbonyl
  40204. ylide
  40205. organic
  40206. synthesis
  40207. fluoride
  40208. derivative
  40209. thiocarbonyl
  40210. ylides
  40211. thiocarbonyldiimidaz
  40212. thiochalcones
  40213. thiocyanates
  40214. thioenamide
  40215. thioenol
  40216. thioester
  40217. thioesters
  40218. thioether
  40219. thioethers
  40220. thioglycolate
  40221. thioglycosides
  40222. thiohydroxamic
  40223. thiohydroxamic
  40224. esters
  40225. homoallylic
  40226. alcohols
  40227. chain
  40228. reactions
  40229. thioimide
  40230. thioiumion
  40231. thioketen
  40232. thioketene
  40233. thioketene
  40234. acetal
  40235. thioketones
  40236. thiol
  40237. thiolactam
  40238. thiolate
  40239. thiolesters
  40240. thiols
  40241. thionation
  40242. thione
  40243. thiones
  40244. thionins
  40245. thionitroso
  40246. thionitrosoarenes
  40247. thionitrosoarenes
  40248. diels
  40249. alder
  40250. arylaminothio
  40251. phthalim
  40252. thionium
  40253. thiono
  40254. thiono
  40255. lactone
  40256. thionyl
  40257. thionyl
  40258. chloride
  40259. thiophene
  40260. thiophene
  40261. reduction
  40262. thiophene-2-carboxyl
  40263. thiophenophanes
  40264. furanophanes
  40265. pyridinophanes
  40266. pyrimidinophanes
  40267. thiophenoxide
  40268. thiophenyl
  40269. thiophosgene
  40270. thiophynes
  40271. thiopyran
  40272. thiopyrans
  40273. thiopyrans
  40274. benzothiopyrans
  40275. thioxanthenes
  40276. dibenzothiopyrans
  40277. thiotetralones
  40278. thiourea
  40279. thioxanthenes
  40280. thoethers
  40281. tholactam
  40282. removal
  40283. three
  40284. threitol
  40285. threo
  40286. threonine
  40287. thrombin
  40288. thromboxanes
  40289. thummel
  40290. thummel
  40291. benzocyclobutene
  40292. extrusion
  40293. cycloaddition
  40294. synthesis
  40295. catalyzed
  40296. epoxidation
  40297. ticl4
  40298. tidwell
  40299. tidwell
  40300. carbonium
  40301. cation
  40302. review
  40303. solvolysis
  40304. kinetics
  40305. unstable
  40306. chemistry
  40307. chloride
  40308. elimination
  40309. enolate
  40310. fluoride
  40311. hydride
  40312. hydride
  40313. radicals
  40314. hydrostannation
  40315. hydrostannolysis
  40316. chloride
  40317. lewis
  40318. mediated
  40319. asymmetric
  40320. aldol
  40321. reaction
  40322. ketyl
  40323. radical
  40324. lithium
  40325. exchange
  40326. alpha
  40327. alkoxy
  40328. stannane
  40329. organolithium
  40330. reagent
  40331. stannane
  40332. ether
  40333. cleavage
  40334. ozone
  40335. oxidation
  40336. carbonyl
  40337. ketone
  40338. tetrabromide
  40339. tetrachloride
  40340. tiogenic
  40341. tional
  40342. tions
  40343. tishchenko
  40344. tishchenko
  40345. reaction
  40346. tisler
  40347. tisler
  40348. amidine
  40349. heterocycle
  40350. synthesis
  40351. cyclization
  40352. review
  40353. titanacycle
  40354. titanacycle
  40355. titanacyclobutane
  40356. titanacyclopropane
  40357. titaniumH
  40358. titanium
  40359. carbonyl
  40360. coupling
  40361. titanium
  40362. catalyst
  40363. titanium
  40364. catalyzed
  40365. michael
  40366. addition
  40367. allyltrimethylsilane
  40368. titanium
  40369. chemistry
  40370. titanium
  40371. chloride
  40372. catalyst
  40373. titanium
  40374. complex
  40375. titanium
  40376. enolate
  40377. titanium
  40378. enolates
  40379. enantioselective
  40380. hydroxylation
  40381. titanium
  40382. isopropoxide
  40383. titanium
  40384. lewis
  40385. titanium
  40386. lewis
  40387. titanium
  40388. mediated
  40389. cyclization
  40390. titanium
  40391. oxazolidinone
  40392. enolate
  40393. titanium
  40394. reagent
  40395. titanium
  40396. tetrachloride
  40397. titanium
  40398. tetraisopropoxide
  40399. titanocene
  40400. tjipanazole
  40401. tjipanazole
  40402. tmeda
  40403. methyl
  40404. tms2s
  40405. tmsbr
  40406. tmschn2
  40407. tmscl
  40408. tmscn
  40409. tmsotf
  40410. tmsotf
  40411. mediated
  40412. closure
  40413. toluidines
  40414. tolyl
  40415. topics
  40416. topoisomerase
  40417. topological
  40418. topolski
  40419. torquoselectivity
  40420. torsion
  40421. torssell
  40422. torssell
  40423. dipolar
  40424. cycloaddition
  40425. isoxazolidine
  40426. nitrile
  40427. nitrone
  40428. tosmic
  40429. tosmic
  40430. reagent
  40431. pyrrole
  40432. preparation
  40433. sulfone
  40434. heterocycle
  40435. revie
  40436. tosyl
  40437. tosyl
  40438. enamine
  40439. tosyl
  40440. hydrazone
  40441. tosylamine
  40442. tosylate
  40443. tosylation
  40444. tosylbutenone
  40445. tosylhydrazone
  40446. tosylhydrazones
  40447. tosylimines
  40448. tosyloxy
  40449. tosyloxycarbamate
  40450. tosylpropene
  40451. total
  40452. total
  40453. toxic
  40454. toxic
  40455. cyclic
  40456. peptide
  40457. biologically
  40458. active
  40459. cyclopeptides
  40460. amino
  40461. toxicants
  40462. toxin
  40463. oxidation
  40464. trajectoryI
  40465. trans
  40466. trans
  40467. b-lactam
  40468. trans
  40469. trans
  40470. hydrogenation
  40471. acetylene
  40472. trans
  40473. parinaric
  40474. polyene
  40475. fatty
  40476. acids
  40477. fluorescent
  40478. probes
  40479. trans
  40480. selectivity
  40481. trans-25-dimethylpyr
  40482. transannular
  40483. transannular
  40484. hydride
  40485. migration
  40486. transcriptase
  40487. ransesterification
  40488. diastereoselective
  40489. intramolecular
  40490. cycloa
  40491. transfer
  40492. transfer
  40493. actions
  40494. allylic
  40495. abstraction
  40496. transfer
  40497. cyclization
  40498. reactions
  40499. alpha
  40500. esters
  40501. transf
  40502. transfer
  40503. photooxygenation
  40504. rearrangement
  40505. mechanism
  40506. oxyge
  40507. transfo
  40508. transformat
  40509. transformatio
  40510. transformation
  40511. transformations
  40512. transient
  40513. transition
  40514. transition
  40515. transition
  40516. metal
  40517. transition
  40518. metal
  40519. alkylidene
  40520. transition
  40521. metal
  40522. annulation
  40523. cycloaddition
  40524. transition
  40525. metal
  40526. carbene
  40527. complex
  40528. transition
  40529. metal
  40530. catalysis
  40531. nolate
  40532. transition
  40533. metal
  40534. transition
  40535. metal
  40536. mediated
  40537. annulation
  40538. transition
  40539. metal
  40540. reductive
  40541. cyclization
  40542. transition
  40543. metal
  40544. sequenes
  40545. transition
  40546. metal
  40547. transfer
  40548. hydrogenation
  40549. translocation
  40550. translocation
  40551. radical
  40552. alpha
  40553. amino
  40554. radical
  40555. formation
  40556. transmetalation
  40557. talation
  40558. hydrocarbons
  40559. transmetallation
  40560. transmission
  40561. transposed
  40562. transposition
  40563. trapping
  40564. treated
  40565. triacetate
  40566. triacetates
  40567. triacetoxyborohydrid
  40568. trialkylaluminum
  40569. trialkylstannylmethy
  40570. trialkysilyl
  40571. triamide
  40572. triarylcarbenium
  40573. triarylsilylmethylme
  40574. triazabicyclo
  40575. triazaphenanthrenes
  40576. triazene
  40577. triazene
  40578. diazonium
  40579. iodide
  40580. phenyl
  40581. thermal
  40582. metho
  40583. triazepines
  40584. triazetidines
  40585. triazine
  40586. triazine
  40587. amidine
  40588. diels
  40589. alder
  40590. heterocycle
  40591. extrusion
  40592. inver
  40593. triazines
  40594. triazines
  40595. benzotriazines
  40596. naphthotriazines
  40597. triazines
  40598. cyanuric
  40599. melamines
  40600. ammelines
  40601. ammelides
  40602. acetog
  40603. triazocines
  40604. triazole
  40605. triazole
  40606. metalation
  40607. triazole-1
  40608. triazoles
  40609. triazoline
  40610. triazolinedione
  40611. triazolium
  40612. triazoloisoquinoline
  40613. triazolooxadiazoles
  40614. triazolophthalazines
  40615. triazolopyrazines
  40616. triazolopyridazines
  40617. triazolopyridines
  40618. triazolopyridines
  40619. triazolopyridazines
  40620. triazolopyrimidines
  40621. triazolopyrimidines
  40622. triazoloquinazolines
  40623. triazoloquinolines
  40624. triazoloquinoxalines
  40625. triazoloselenadiazol
  40626. triazolothiadiazoles
  40627. triazolotriazines
  40628. triazolotriazoles
  40629. tribal
  40630. tribromide
  40631. tribut
  40632. tributyl
  40633. tributyl
  40634. antimonate
  40635. tributyl
  40636. phosphine
  40637. tributyl
  40638. hydride
  40639. tributylfin
  40640. tributyltin
  40641. tributyltin
  40642. cyanide
  40643. tributyltin
  40644. hydride
  40645. tributyltin
  40646. hydride
  40647. cleavage
  40648. acids
  40649. tricarbonyl
  40650. tricarbonyl
  40651. review
  40652. photochem
  40653. diazo
  40654. diels
  40655. alder
  40656. tetraketone
  40657. tricarbonyl
  40658. synthesis
  40659. tricarbonyliron
  40660. tricarboxylates
  40661. trichloride
  40662. trichloro
  40663. trichloroacetimidate
  40664. trichloroethoxyester
  40665. trichloroethyl
  40666. trichloromethyl
  40667. trichloromethyl
  40668. lithium
  40669. trichloromethylation
  40670. trichlorosilane
  40671. trichoverrin
  40672. tricyclic
  40673. triene
  40674. triene
  40675. synthesis
  40676. boron
  40677. initiated
  40678. radical
  40679. cyclization
  40680. triethylaluminum
  40681. triethylamine
  40682. triethylborane
  40683. triethylborohydride
  40684. triethylsilane
  40685. tributyltin
  40686. trienes@
  40687. triethylsilane
  40688. reduction@
  40689. triflamides@
  40690. triflate
  40691. pyridine
  40692. coupling
  40693. cross
  40694. silyl
  40695. alkynyl
  40696. stille
  40697. trifluoromethylthio
  40698. carbon
  40699. carbenium
  40700. electron
  40701. oxida@
  40702. trimethylchlorosilan@
  40703. trimethylsilyldiazom@
  40704. triterpenes@
  40705. trixolanes@
  40706. trost@
  40707. turchi
  40708. heterocycle
  40709. review
  40710. oxazole
  40711. reaction
  40712. heterocycle
  40713. rearr@
  40714. types@
  40715. umpolung
  40716. review
  40717. synthon
  40718. unsaturated
  40719. carbenes
  40720. generation
  40721. wittig
  40722. reaction
  40723. vinyl
  40724. ureas
  40725. variable@
  40726. various
  40727. vilsmeier-haack@
  40728. vinyl
  40729. vinyl
  40730. boronic
  40731. ester@
  40732. vinyl
  40733. cyclopropane
  40734. cyclopentene
  40735. carbanion
  40736. sulfone
  40737. rearrangem@
  40738. vinyl
  40739. iodide
  40740. synthesis@
  40741. vinyl
  40742. substitution
  40743. reactions
  40744. halides
  40745. stereocontrolled
  40746. diels
  40747. alder
  40748. review
  40749. heterocycle
  40750. imine
  40751. cycloadditi@
  40752. wiersum
  40753. flash
  40754. review
  40755. pyrolysis
  40756. vacuum
  40757. synthesis
  40758. writing@
  40759. wilkinson's@
  40760. wittig
  40761. cyano
  40762. phosphorous
  40763. dicarbonyl
  40764. chloride
  40765. triflamides
  40766. triflate
  40767. silyl
  40768. alkynyl
  40769. stille
  40770. triflates
  40771. triflating
  40772. triflic
  40773. triflic
  40774. triflic
  40775. anhydride
  40776. triflones
  40777. triflouride
  40778. trifluoride
  40779. trifluoro
  40780. trifluoroacetata
  40781. trifluoroacetate
  40782. trifluoroacetic
  40783. trifluoroacetic
  40784. trifluoromethanesulf
  40785. trifluoromethanesulf
  40786. trifluoroacetic
  40787. hydrazoic
  40788. trifluoromethanesulf
  40789. lewis
  40790. reagent
  40791. complexes
  40792. trifluoromethanesulp
  40793. trifluoromethyl
  40794. trifluoromethyl
  40795. sulfones
  40796. organic
  40797. synthesis
  40798. trifluoromethylthio
  40799. trifluoromethylthio
  40800. carbon
  40801. carbenium
  40802. electron
  40803. oxida
  40804. trifluoromethyltrime
  40805. trigger
  40806. triggering
  40807. triisobutylaluminium
  40808. triketone
  40809. trimethyl
  40810. trimethyl
  40811. aluminum
  40812. trimethyl
  40813. stannyl
  40814. lithium
  40815. trimethylaluminium
  40816. trimethylaluminum
  40817. methylchlorosilan
  40818. trimethylene
  40819. trimethylenemethane
  40820. trimethyliodosilane
  40821. trimethylsilane
  40822. trimethylsilanolate
  40823. trimethylsilyl
  40824. trimethylsilyl
  40825. azide
  40826. trimethylsilyl
  40827. chloride
  40828. trimethylsilyl
  40829. crystal
  40830. structures
  40831. molecular
  40832. structure
  40833. trimethylsilyl
  40834. ethers
  40835. active
  40836. steroids
  40837. lithium
  40838. trimethylsilyl
  40839. ether
  40840. trimethylsilyl
  40841. triflate
  40842. trimethylsilylazide
  40843. trimethylsilylcyclop
  40844. trimethylsilylcyclop
  40845. annulation
  40846. stereoselective
  40847. synthesis
  40848. trimethylsilyldiazom
  40849. trimethylsilyltrifla
  40850. trimethylspiro
  40851. triol
  40852. triol
  40853. synthesis
  40854. trione
  40855. trioxane
  40856. trioxanes
  40857. trioxide
  40858. trioxocanes
  40859. trioxolane
  40860. trioxolanes
  40861. triphenylarsine
  40862. triphenylmethyl
  40863. triphenylphosphine
  40864. triphenylphosphine
  40865. dibromide
  40866. triphenylphosphine
  40867. ligand
  40868. triphenylphosphorany
  40869. triplet
  40870. triplet
  40871. nitrogen
  40872. molecules
  40873. acylation
  40874. tripodal
  40875. trippett
  40876. trippett
  40877. review
  40878. methodology
  40879. phospherane
  40880. wittig
  40881. betaine
  40882. ylide
  40883. triquinane
  40884. triquinanes
  40885. trimethylsilyl
  40886. silane
  40887. trishomocubanes
  40888. trispiro
  40889. trisub
  40890. trisubstituted
  40891. trisubstituted
  40892. alkenes
  40893. trisyl
  40894. trisyl
  40895. azide
  40896. trithiolanes
  40897. tritration
  40898. trityl
  40899. trityl
  40900. cation
  40901. trityl
  40902. ether
  40903. trityl
  40904. perchlorate
  40905. trivalent
  40906. trixolanes
  40907. trixolanes
  40908. trithiolanes
  40909. dioxathiolanes
  40910. oxadithiolanes
  40911. dioxat
  40912. tropane
  40913. tropolone
  40914. tropone
  40915. tropone
  40916. synthesis
  40917. trost
  40918. review
  40919. cycloaddition
  40920. organometallic
  40921. cyclopentane
  40922. trost
  40923. review
  40924. transition
  40925. metal
  40926. catalyst
  40927. palladium
  40928. metal
  40929. trost
  40930. stereochem
  40931. carbanion
  40932. sulfone
  40933. asymmetric
  40934. alkylation
  40935. trost
  40936. sulfur
  40937. ether
  40938. preparation
  40939. alkylation
  40940. carbanio
  40941. tryptamine
  40942. tryptophan
  40943. tryptophan
  40944. dimer
  40945. tsuge
  40946. tsuji
  40947. tsuji
  40948. alkene
  40949. terminal
  40950. oxidation
  40951. methyl
  40952. ketone
  40953. review
  40954. palladi
  40955. tuberculatum
  40956. tubotaiwine
  40957. tufariello
  40958. tufariello
  40959. review
  40960. nitrone
  40961. alkaloid
  40962. synthesis
  40963. target
  40964. dipole
  40965. tumor
  40966. tungsten
  40967. tungsten
  40968. abinitio
  40969. carbene
  40970. molecular
  40971. mechanics
  40972. olefin
  40973. metathe
  40974. tungsten
  40975. carbene
  40976. complex
  40977. tungsten
  40978. carbene
  40979. cpmlex
  40980. turchi
  40981. turchi
  40982. heterocycle
  40983. review
  40984. oxazole
  40985. reaction
  40986. heterocycle
  40987. rearr
  40988. mimetics
  40989. turro
  40990. turro
  40991. review
  40992. energy
  40993. transfer
  40994. abstraction
  40995. dimerization
  40996. turro
  40997. review
  40998. radical
  40999. triplet
  41000. photochem
  41001. mechanism
  41002. reaction
  41003. turro
  41004. theory
  41005. photochem
  41006. adiabatic
  41007. review
  41008. physical
  41009. organic
  41010. tussock
  41011. tylosin
  41012. tyrosine
  41013. uchida
  41014. uchida
  41015. review
  41016. pressure
  41017. cycloaddition
  41018. writing
  41019. introducti
  41020. uction
  41021. ullman
  41022. ullmann
  41023. ullmann
  41024. ether
  41025. synthesis
  41026. ullmann
  41027. macrocyclization
  41028. ultra
  41029. ultrasonically
  41030. ultrasonically
  41031. dispersed
  41032. potassium
  41033. metal
  41034. promoted
  41035. reactions
  41036. ultrasonically
  41037. dispersed
  41038. potassium
  41039. nozaki
  41040. hiyama
  41041. reaction
  41042. ultrasound
  41043. umpolung
  41044. umpolung
  41045. review
  41046. synthon
  41047. unactivated
  41048. unactivated
  41049. p-system
  41050. unctional
  41051. unctional
  41052. groups
  41053. oxidation
  41054. alkenes
  41055. alkynes
  41056. undeca
  41057. undecane
  41058. unfunctionalized
  41059. unfunctionalized
  41060. olefins
  41061. asymmetric
  41062. epoxidation
  41063. porphyrins
  41064. unfunctionalized
  41065. olefins
  41066. asymmetric
  41067. epoxidation
  41068. porphyrins
  41069. units
  41070. unnatural
  41071. unprotected
  41072. unsaturated
  41073. unsaturated
  41074. carboxylic
  41075. unsaturated
  41076. esters
  41077. unsaturated
  41078. ketone
  41079. unsaturated
  41080. rhodium
  41081. ketone
  41082. diazo
  41083. insertion
  41084. review
  41085. cyclopente
  41086. unsaturated
  41087. sulfone
  41088. conjugate
  41089. addition
  41090. vinyl
  41091. enone
  41092. novel
  41093. unstable
  41094. unsymmetrical
  41095. unsymmetrization
  41096. unusual
  41097. ureas
  41098. ureas
  41099. ureidoalkylation
  41100. urethane
  41101. urethane
  41102. alkylation
  41103. urethane
  41104. cyclization
  41105. urethanes
  41106. urine
  41107. urrutia
  41108. useful
  41109. useful
  41110. fragments
  41111. heterocy
  41112. l-malic
  41113. l-aspartic
  41114. useful
  41115. reagent
  41116. chloromethyl
  41117. tosylpropene
  41118. using
  41119. ustus
  41120. utility
  41121. utimoto
  41122. utimoto
  41123. reagent
  41124. silicon
  41125. nitrile
  41126. cyano
  41127. cyanotrimethylsilane
  41128. laser
  41129. photochemistry
  41130. triplet
  41131. diradicals
  41132. azoalkanes
  41133. vacuum
  41134. valence
  41135. valerolactones
  41136. valinol
  41137. leusen
  41138. review
  41139. tosmic
  41140. heterocycle
  41141. oxazole
  41142. rearrangement
  41143. leusen
  41144. review
  41145. tosmic
  41146. reagent
  41147. nitrile
  41148. heterocycle
  41149. pyrrole
  41150. vanadium
  41151. vanadium
  41152. catalyzed
  41153. vanadium
  41154. chemistry
  41155. vanadium
  41156. salts
  41157. vanloon
  41158. varacin
  41159. variety
  41160. various
  41161. various
  41162. various
  41163. radical
  41164. ketyl
  41165. cyclization
  41166. samarium
  41167. varvoglis
  41168. varvoglis
  41169. review
  41170. iodine
  41171. synthesis
  41172. hypervalent
  41173. iodination
  41174. veeranaghanan
  41175. venom
  41176. verboom
  41177. vermiculine
  41178. verrucarin
  41179. versatile
  41180. versatile
  41181. amidoalkylation
  41182. reagents
  41183. versatile
  41184. amidoalkylation
  41185. reagents
  41186. sulfonylated
  41187. hydroxamic
  41188. version
  41189. versus
  41190. vibration
  41191. vicinal
  41192. viehe
  41193. viehe
  41194. captodative
  41195. merostabilization
  41196. radical
  41197. dimerization
  41198. viehe
  41199. iminium
  41200. review
  41201. cyclization
  41202. heterocycle
  41203. viehe
  41204. review
  41205. captodative
  41206. merostabilization
  41207. radical
  41208. stability
  41209. viehe
  41210. ynamine
  41211. review
  41212. amino
  41213. alkyne
  41214. amine
  41215. preparation
  41216. villiger
  41217. eier-haack
  41218. vinamidinium
  41219. vinamidinium
  41220. vinblastine
  41221. vinca
  41222. vincadifformine
  41223. vindoline
  41224. vinlysilane
  41225. vinylD
  41226. vinyl
  41227. vinyl
  41228. allene
  41229. carbenoid
  41230. diazo
  41231. rhodium
  41232. mechanism
  41233. stepwise
  41234. terminus
  41235. vinyl
  41236. cations
  41237. rearrangement
  41238. vinyl
  41239. cerium
  41240. addition
  41241. ketone
  41242. vinyl
  41243. copper
  41244. vinyl
  41245. cuprates
  41246. vinyl
  41247. cyclopropane
  41248. cyclopentene
  41249. carbanion
  41250. sulfone
  41251. rearrangem
  41252. vinyl
  41253. cyclopropane
  41254. cyclopentene
  41255. rearrangement
  41256. review
  41257. thermal
  41258. vinyl
  41259. epoxide
  41260. opening
  41261. cuprate
  41262. displacement
  41263. substitution
  41264. vinyl
  41265. epoxides
  41266. vinyl
  41267. ether
  41268. vinyl
  41269. ethers
  41270. vinyl
  41271. grignard
  41272. coupling
  41273. vinyl
  41274. halide
  41275. vinyl
  41276. iodide
  41277. vinyl
  41278. lithium
  41279. vinyl
  41280. lithium
  41281. aldehyde
  41282. coupling
  41283. vinyl
  41284. lithium
  41285. reagent
  41286. vinyl
  41287. lithium
  41288. species
  41289. vinyl
  41290. metal
  41291. vinyl
  41292. radical
  41293. cyclization
  41294. vinyl
  41295. radicals
  41296. vinyl
  41297. rearrangement
  41298. allene
  41299. diels
  41300. alder
  41301. cyclization
  41302. intramole
  41303. vinyl
  41304. silane
  41305. vinyl
  41306. silane
  41307. n-sulfonyliminium
  41308. closure
  41309. vinyl
  41310. stannane
  41311. vinyl
  41312. stannane
  41313. bromo
  41314. borane
  41315. exchange
  41316. vinyl
  41317. borane
  41318. cycloaddit
  41319. vinyl
  41320. substitution
  41321. reactions
  41322. halides
  41323. stereocontrolled
  41324. vinyl
  41325. substitution
  41326. reactions
  41327. halides
  41328. stereocontrolled
  41329. vinyl
  41330. sulfde
  41331. vinyl
  41332. sulfide
  41333. vinyl
  41334. sulfide
  41335. formation
  41336. vinyl
  41337. sulfone
  41338. vinyl
  41339. sulfone
  41340. conjugate
  41341. addition
  41342. preparation
  41343. review
  41344. desulfon
  41345. vinyl
  41346. sulfoxide
  41347. cycloadditions
  41348. equivalents
  41349. cycloadditions
  41350. vinyl
  41351. sulfoxides
  41352. cyclopentadiene
  41353. dienophiles
  41354. vinyl
  41355. tellurides
  41356. vinyl
  41357. vinyl
  41358. compound
  41359. vinyl
  41360. triphenylphosphine
  41361. intermediate
  41362. vinylallenes
  41363. vinylation
  41364. vinylcarbene
  41365. vinylcarbenes
  41366. vinylcuprate
  41367. vinylcyclopropane
  41368. vinylcyclopropanes
  41369. vinylcyclopropene
  41370. vinylepoxides
  41371. vinylic
  41372. vinylidene
  41373. vinylidene
  41374. carbene
  41375. vinylidene
  41376. rearrangements
  41377. isomerization
  41378. intermediacy
  41379. acetyle
  41380. vinylimino
  41381. vinylimino
  41382. phosphoranes
  41383. vinyliminophosphoran
  41384. vinylin
  41385. vinylin
  41386. vinylindoles
  41387. vinylketene
  41388. vinyllithium
  41389. vinylogous
  41390. vinylogous
  41391. amide
  41392. vinylphosphonates
  41393. vinylsilane
  41394. vinylsilanes
  41395. vinylstannanes
  41396. vinylstannanes
  41397. alpha
  41398. stannyl
  41399. enones
  41400. photooxygenation
  41401. allylic
  41402. vinylstannanes
  41403. photooxygenation
  41404. schenck
  41405. reaction
  41406. hydroxy
  41407. vinylthioether
  41408. vinyltin
  41409. vinyltin
  41410. cyclization
  41411. vinylzirconation
  41412. viola
  41413. viola
  41414. pericyclic
  41415. alkyne
  41416. sigmatropic
  41417. rearrangement
  41418. cyclizatio
  41419. viola
  41420. review
  41421. flash
  41422. alkyne
  41423. electrocyclic
  41424. intramolecular
  41425. carbe
  41426. virus
  41427. viscosity
  41428. vitamin
  41429. vitro
  41430. vollhardt
  41431. vollhardt
  41432. diels
  41433. alder
  41434. intramolecular
  41435. cycloaddition
  41436. review
  41437. volume
  41438. wacker
  41439. wacker
  41440. oxidation
  41441. wadsworth
  41442. wadsworth-emmons
  41443. wagner
  41444. wagner
  41445. photochem
  41446. hydrogen
  41447. abstraction
  41448. review
  41449. ketone
  41450. delta
  41451. wagner-meerwein
  41452. wakefield
  41453. wakefield
  41454. isoxazole
  41455. review
  41456. chemistry
  41457. biology
  41458. rearrangeme
  41459. walborsky
  41460. waldmann
  41461. walker
  41462. wallace
  41463. wallace
  41464. review
  41465. hydroxyl
  41466. amine
  41467. sulfonic
  41468. reagent
  41469. amine
  41470. wallbaum
  41471. wallbaum
  41472. oxazaborolidine
  41473. review
  41474. chiral
  41475. reduction
  41476. cycloadditi
  41477. warkentin
  41478. warkentin
  41479. carbene
  41480. ylide
  41481. heteroatom
  41482. addition
  41483. trapping
  41484. review
  41485. warrener
  41486. warrener
  41487. wasserman
  41488. wasserman
  41489. singlet
  41490. oxygen
  41491. synthesis
  41492. reaction
  41493. peroxide
  41494. waste
  41495. water
  41496. water
  41497. water
  41498. hydrophobic
  41499. effects
  41500. aqueous
  41501. media
  41502. reactivity
  41503. water
  41504. nitrile
  41505. carbanion
  41506. oxygen
  41507. oxygenation
  41508. alkylation
  41509. review
  41510. weinreb
  41511. weinreb
  41512. amide
  41513. weinreb
  41514. diels
  41515. alder
  41516. hetero
  41517. imine
  41518. review
  41519. alkaloid
  41520. imine
  41521. cyclo
  41522. weinreb
  41523. diels
  41524. alder
  41525. review
  41526. heterocycle
  41527. imine
  41528. cycloadditi
  41529. weinreb
  41530. diels
  41531. alder
  41532. review
  41533. heterocycle
  41534. imine
  41535. carbonyl
  41536. cycloa
  41537. weinreb's
  41538. weinreb's
  41539. amide
  41540. wender
  41541. wender
  41542. intramolecular
  41543. dipolar
  41544. cycloaddition
  41545. dipole
  41546. carbonyl
  41547. wender
  41548. review
  41549. methodology
  41550. macrocycle
  41551. expansion
  41552. medium
  41553. wenkert
  41554. wentrup
  41555. wentrup
  41556. flash
  41557. review
  41558. writing
  41559. pyrolysis
  41560. sigmatropic
  41561. reactive
  41562. wentrup
  41563. review
  41564. nitrene
  41565. carbene
  41566. intramolecular
  41567. addition
  41568. inser
  41569. wentrup
  41570. review
  41571. rearrangement
  41572. reactive
  41573. intermediate
  41574. carbene
  41575. wenzel
  41576. wenzel
  41577. review
  41578. spectroscopy
  41579. shift
  41580. reagent
  41581. metal
  41582. europium
  41583. werner
  41584. werstiuk
  41585. werstiuk
  41586. review
  41587. enolate
  41588. homoenolate
  41589. anion
  41590. mechanism
  41591. which
  41592. whitesell
  41593. whitesell
  41594. chiral
  41595. auxiliary
  41596. ligand
  41597. review
  41598. whitesell
  41599. enolate
  41600. imine
  41601. hydrazone
  41602. carbanion
  41603. alkylation
  41604. revie
  41605. wicha
  41606. wicha
  41607. silicon
  41608. silyl
  41609. epoxide
  41610. anion
  41611. group
  41612. transfer
  41613. rearrangeme
  41614. wiersum
  41615. wiersum
  41616. flash
  41617. review
  41618. pyrolysis
  41619. vacuum
  41620. synthesis
  41621. writing
  41622. wiesner
  41623. wiesner
  41624. stereochem
  41625. photocycloaddition
  41626. alkene
  41627. cyclobutan
  41628. wilen
  41629. wilkinson
  41630. wilkinson
  41631. catalyst
  41632. nson's
  41633. wilkinson's
  41634. catalyst
  41635. willgerodt
  41636. williams
  41637. williams
  41638. alpha
  41639. amino
  41640. acids
  41641. chiral
  41642. enolate
  41643. glycine
  41644. oxazinone
  41645. williams
  41646. asymmetric
  41647. alkylation
  41648. glycine
  41649. enolate
  41650. review
  41651. wilson
  41652. wilson
  41653. review
  41654. sulfur
  41655. sulfonium
  41656. pummerer
  41657. halogen
  41658. without
  41659. witkop
  41660. wittenberger
  41661. wittenberger
  41662. wittig
  41663. wittig
  41664. cyano
  41665. phosphorous
  41666. dicarbonyl
  41667. chloride
  41668. wittig
  41669. macrolactamization
  41670. wittig
  41671. olefination
  41672. wittig
  41673. reaction
  41674. wittig
  41675. reaction
  41676. afford
  41677. allene
  41678. wittig
  41679. reactions
  41680. ylides
  41681. wittig
  41682. rearrangement
  41683. rrangement
  41684. wittig
  41685. theory
  41686. stereochemistry
  41687. review
  41688. writing
  41689. betaine
  41690. phospho
  41691. witzeman
  41692. wolff
  41693. wolff
  41694. rearrangement
  41695. arene
  41696. extrusion
  41697. alkyne
  41698. furan
  41699. cycloaddition
  41700. aromatic
  41701. sugar
  41702. enzyme
  41703. glycoprocessing
  41704. inhibitors
  41705. review
  41706. cyclopropane
  41707. review
  41708. synthesis
  41709. small
  41710. strain
  41711. target
  41712. deoxygenation
  41713. titanium
  41714. review
  41715. isobenzofuran
  41716. alkyne
  41717. woodward
  41718. writing
  41719. writing
  41720. writing
  41721. alcohol
  41722. review
  41723. diketene
  41724. dioxinone
  41725. acetoacetylation
  41726. writing
  41727. review
  41728. allyl
  41729. cycloaddition
  41730. wuest
  41731. wuest
  41732. epoxide
  41733. opening
  41734. review
  41735. cyclopropane
  41736. eliminati
  41737. wulff
  41738. crystal
  41739. asymmetrically
  41740. substituted
  41741. calix
  41742. arene
  41743. ionop
  41744. diffraction
  41745. structure
  41746. structure
  41747. carbon
  41748. formation
  41749. complexes
  41750. compounds
  41751. potential
  41752. dipoles
  41753. amino
  41754. acids
  41755. ninhydrin
  41756. x-c-c-y
  41757. x-c-m
  41758. x-ray
  41759. crystal
  41760. structure
  41761. heterocyclic
  41762. compounds
  41763. latent
  41764. x-ray
  41765. crystal
  41766. structure
  41767. nuclear
  41768. magnetic
  41769. resonance
  41770. organocop
  41771. xadiazolines
  41772. xadiazolines
  41773. oxadiazolidines
  41774. xanthate
  41775. xanthates
  41776. xanthenes
  41777. xanthines
  41778. xanthones
  41779. xestoquinone
  41780. xestospongia
  41781. xylene
  41782. xylidines
  41783. yamada
  41784. yamada
  41785. alkaloid
  41786. synthesis
  41787. cancer
  41788. writing
  41789. review
  41790. yamaguchi
  41791. yamaguchi
  41792. yamamotoE
  41793. yamamoto
  41794. cuprate
  41795. iridine
  41796. introduE
  41797. yamamoto
  41798. experimental
  41799. michael
  41800. conjugate
  41801. addition
  41802. review
  41803. yamamoto
  41804. method
  41805. aldol
  41806. asymmetric
  41807. review
  41808. chiral
  41809. metal
  41810. chelation
  41811. evans
  41812. ybcl3
  41813. yclic
  41814. yeast
  41815. yields
  41816. ylates
  41817. ylide
  41818. ylides
  41819. ylids
  41820. ylium
  41821. yllithium
  41822. ynamine
  41823. ynamines
  41824. ynamines
  41825. trimethylsilyl
  41826. cycloaddition
  41827. reactions
  41828. yokoyama
  41829. yokoyama
  41830. carbon
  41831. disulfide
  41832. review
  41833. reagent
  41834. reference
  41835. yokuyama
  41836. yokuyama
  41837. review
  41838. sulfur
  41839. carbon
  41840. disulfide
  41841. addition
  41842. yoshikoshi
  41843. yoshikoshi
  41844. nitro
  41845. alkene
  41846. conjugate
  41847. addition
  41848. review
  41849. silyl
  41850. ytterbium
  41851. ytterbium
  41852. chiral
  41853. lewis
  41854. ytterbium
  41855. triflate
  41856. sulfone
  41857. vinyl
  41858. review
  41859. carbanion
  41860. addition
  41861. carbonyl
  41862. alkoxid
  41863. zaugg
  41864. alkylation
  41865. amide
  41866. synthesis
  41867. review
  41868. nucleophilic
  41869. substit
  41870. zearalenone
  41871. zeaxanthin
  41872. zeolite
  41873. review
  41874. asymmetric
  41875. ester
  41876. hydrolysis
  41877. enzyme
  41878. reagent
  41879. ziconium
  41880. ziconium
  41881. complex
  41882. ziegler
  41883. ziegler
  41884. review
  41885. claisen
  41886. rearrangement
  41887. regiochem
  41888. stereochem
  41889. ziegler
  41890. review
  41891. thermal
  41892. rearrangement
  41893. claisen
  41894. aliphatic
  41895. synth
  41896. zielger-natta
  41897. zielger-natta
  41898. catalyst
  41899. zimmerman
  41900. zimmerman
  41901. methane
  41902. photorearrangement
  41903. synthesis
  41904. stereoc
  41905. borohydride/silica
  41906. bromide
  41907. chloride
  41908. complex
  41909. compound
  41910. enolate
  41911. trapping
  41912. powder
  41913. cyclization
  41914. palladium
  41915. cephems
  41916. alkenyl
  41917. insit
  41918. reagent
  41919. species
  41920. triflate
  41921. zinin
  41922. zircoceneF
  41923. zirconacyclopentane
  41924. zirconacyclopentane
  41925. zirconiumF
  41926. zirconium
  41927. catalyst
  41928. conium
  41929. organozirconium
  41930. zirconium
  41931. silicon
  41932. metallocenes
  41933. carbon
  41934. carbon
  41935. formation
  41936. zirconoceneF
  41937. zirconocene
  41938. benzyne
  41939. complex
  41940. allyl
  41941. amine
  41942. insertion
  41943. indoline
  41944. zirconocene
  41945. equivalent
  41946. allylic
  41947. zirconium
  41948. species
  41949. alkoxy
  41950. zn-cu
  41951. zn/cu
  41952. zn/cu
  41953. couple
  41954. electroreduction
  41955. conjugate
  41956. addition
  41957. olefins
  41958. zwanenburg
  41959. zwanenburg
  41960. sulfur
  41961. sulfene
  41962. review
  41963. preparation
  41964. cycloaddition
  41965. zwitterion
  41966. catalyst
  41967. acylindoles
  41968. react
  41969. regioselectively
  41970. halogenoacyl
  41971. phenyl
  41972. thioalkyl
  41973. secondaryamino
  41974. diaza
  41975. methylcarbapenems
  41976. synthesized
  41977. utilizing
  41978. esche
  41979. meyers
  41980. tetrahedron
  41981. meyers
  41982. 20916
  41983. other
  41984. example
  41985. overall
  41986. yield
  41987. phenyl
  41988. dibenzosuberyl
  41989. salts
  41990. efficiently
  41991. catalyze
  41992. substituted
  41993. pyrrolo
  41994. pyridin
  41995. azaindolinones
  41996. 1-158
  41997. catalyst
  41998. ranged
  41999. 80-94
  42000. 1-phenylethylamine
  42001. 1-phenylethylamine
  42002. 1.5:1
  42003. examples
  42004. 45-96
  42005. yields
  42006. examples
  42007. 55-95
  42008. yield@
  42009. 1234@
  42010. 14-syn@
  42011. other
  42012. examples
  42013. furan
  42014. titlecompoun@
  42015. cyclopentenyl
  42016. hydroxy
  42017. benzopyran
  42018. acet@
  42019. examples
  42020. furanone
  42021. synthesis
  42022. electrophilc
  42023. 55-90@
  42024. other
  42025. examples
  42026. 41-87
  42027. chlorovinyl
  42028. alcohols
  42029. 19-77
  42030. 71-100@
  42031. examples
  42032. yields
  42033. 58-98
  42034. 73-92@
  42035. conceptually
  42036. attractive
  42037. enantioselective
  42038. synthesis@
  42039. versatile
  42040. synthesis
  42041. tetracyclic
  42042. compounds
  42043. synthesis
  42044. thiols
  42045. yield
  42046. utilizing
  42047. carbon
  42048. series
  42049. hexenyllithiums
  42050. having
  42051. phenyl
  42052. trimethylsilyl
  42053. synthetic
  42054. sequence
  42055. preparation
  42056. disubstitute@
  42057. academic@
  42058. accompanied@
  42059. achieves
  42060. acrylate@
  42061. addition
  42062. afford
  42063. examples
  42064. 55-95
  42065. yield
  42066. examples
  42067. 70-90
  42068. 93:7-3:99
  42069. erythro/threo
  42070. examples
  42071. intermolecular
  42072. catalyzed
  42073. coupling
  42074. examples
  42075. systems
  42076. 52-87
  42077. other
  42078. examples
  42079. asymmetric
  42080. diels-alder
  42081. reaction
  42082. 75-99
  42083. 10-91
  42084. yield
  42085. 100:0
  42086. 100mmol
  42087. dibromoalkenes
  42088. bromoalkynes
  42089. alkynes
  42090. could
  42091. obtain
  42092. other
  42093. examples
  42094. 14-81
  42095. yield
  42096. other
  42097. examples
  42098. 32-93
  42099. yield
  42100. other
  42101. examples
  42102. 43-92
  42103. yield
  42104. other
  42105. examples
  42106. 45-85
  42107. other
  42108. examples
  42109. 72-88
  42110. yield
  42111. 111333
  42112. 11:89
  42113. benzenedimethanol
  42114. protecting
  42115. group
  42116. aldehydes
  42117. kibayash
  42118. dibromoethane
  42119. employed
  42120. efficient
  42121. brominati
  42122. examples
  42123. 34-89
  42124. yields
  42125. examples
  42126. 45-75
  42127. yield
  42128. 92-98
  42129. examples
  42130. under
  42131. variety
  42132. conditions
  42133. other
  42134. examples
  42135. 52-86
  42136. yield
  42137. vinylsulfide
  42138. formation
  42139. 68-92
  42140. other
  42141. examples
  42142. 63-90
  42143. yield
  42144. other
  42145. examples
  42146. 77-100
  42147. yields
  42148. 12-98
  42149. 12-addition
  42150. hydroxy
  42151. imino
  42152. methoxy
  42153. trimethy
  42154. examples
  42155. 28-95
  42156. yield
  42157. diastereomeric
  42158. ratio
  42159. examples
  42160. yield
  42161. arylation
  42162. product
  42163. isolated
  42164. other
  42165. examples
  42166. other
  42167. examples
  42168. 53-99
  42169. yield
  42170. 82:18
  42171. 200:1
  42172. other
  42173. examples
  42174. 62-100
  42175. yield
  42176. other
  42177. examples
  42178. yields
  42179. 72-91
  42180. 100:0
  42181. 13-dipolar
  42182. examples
  42183. 40-85
  42184. yield
  42185. examples
  42186. preparations
  42187. boron
  42188. stabilized
  42189. other
  42190. examples
  42191. 35-95
  42192. yield
  42193. other
  42194. examples
  42195. 61-93
  42196. yields
  42197. 14-81
  42198. 14-93
  42199. 14-anti
  42200. 14-hydrostannations
  42201. other
  42202. examples
  42203. 32-82
  42204. yield
  42205. other
  42206. examples
  42207. other
  42208. examples
  42209. 62-94
  42210. yields
  42211. ratios
  42212. 24:76-95:5
  42213. other
  42214. examples
  42215. yield
  42216. syn/anti
  42217. other
  42218. examples
  42219. 70-97
  42220. yield
  42221. 15-44
  42222. 15-91
  42223. examples
  42224. 43-100
  42225. yields
  42226. ranges
  42227. 25/75
  42228. 14-sy
  42229. examples
  42230. 70-99
  42231. 64-93
  42232. yields
  42233. other
  42234. examples
  42235. 15-91
  42236. yield
  42237. other
  42238. examples
  42239. 68-82
  42240. yields
  42241. 89:11-98:2
  42242. 16-83
  42243. examples
  42244. 51-98
  42245. yield
  42246. anti/syn
  42247. ratio
  42248. ranges
  42249. 1977994836
  42250. 198423847
  42251. 1986108
  42252. 1990112
  42253. 1990555553
  42254. 1991113
  42255. 199231
  42256. 199248
  42257. 199248
  42258. 1993115
  42259. 1adducts
  42260. mesitylthio
  42261. alkyl
  42262. benzaldehydes
  42263. their
  42264. dimethylacetal
  42265. photocycloadditions
  42266. between
  42267. enone
  42268. dihydropyran
  42269. additional
  42270. examples
  42271. unusual
  42272. selective
  42273. h3-h1
  42274. allyl
  42275. isomerization
  42276. chiral
  42277. examples
  42278. chiral
  42279. enamine
  42280. 60-91
  42281. yields
  42282. 92-98
  42283. other
  42284. examples
  42285. 68-76
  42286. other
  42287. examples
  42288. yield
  42289. other
  42290. examples
  42291. yields
  42292. 80-86
  42293. tolyloxyfuran
  42294. methoxyfuran
  42295. titlecompoun
  42296. papers
  42297. styryl
  42298. vinyl
  42299. substituted
  42300. methylene
  42301. dioxolanes
  42302. tributylstannyl
  42303. propen
  42304. acetate
  42305. which
  42306. easil
  42307. trimethylsilylmethyl
  42308. methylthio
  42309. methylene
  42310. indanedione
  42311. vinyl
  42312. benzodioxane
  42313. obtained
  42314. 2-chloropyridne
  42315. 2-furyl
  42316. 2-methoxyethylamine
  42317. 2-methoxyethylamine
  42318. 2-no2
  42319. 2.2.1
  42320. 2.2eq
  42321. equivalents
  42322. crcl2
  42323. 2/nabh4
  42324. other
  42325. examples
  42326. 200:1
  42327. 20916873
  42328. examples
  42329. 10-91
  42330. dimethylcyclopropyl
  42331. methylphenyl
  42332. ketone
  42333. presence
  42334. 22-99
  42335. examples
  42336. 25-88
  42337. yield
  42338. ratio
  42339. 65:35
  42340. ferrier
  42341. other
  42342. examples
  42343. yield
  42344. other
  42345. examples
  42346. 16-83
  42347. yield
  42348. other
  42349. examples
  42350. yields
  42351. 12-98
  42352. 23-63
  42353. 23-85
  42354. 2315b
  42355. 242581
  42356. 246810
  42357. 24911
  42358. 24:76-95:5
  42359. other
  42360. examples
  42361. 80-91
  42362. yield
  42363. 25-88
  42364. a-otbs
  42365. b-otbs
  42366. b-otbs
  42367. examples
  42368. yield
  42369. 28-95
  42370. 2khso3
  42371. cyclopentenyl
  42372. hydroxy
  42373. benzopyran
  42374. chloro
  42375. chlorosulfenylchroma
  42376. efficiently
  42377. obtai
  42378. functionalized
  42379. thiophenes
  42380. readily
  42381. prepared
  42382. reactin
  42383. nishizawa
  42384. 242581
  42385. nishizawa
  42386. other
  42387. examples
  42388. 46-74
  42389. yield
  42390. other
  42391. examples
  42392. 70-92
  42393. yield
  42394. diastereoselectivity
  42395. other
  42396. examples
  42397. 70-94
  42398. yield
  42399. syn/anti
  42400. 80:20
  42401. 89:11
  42402. short
  42403. other
  42404. examples
  42405. 95-98
  42406. other
  42407. examples
  42408. yields
  42409. 80-90
  42410. oxovincadifformine
  42411. ethyl
  42412. ester
  42413. synthesized
  42414. 3-hydroxyisoxazole
  42415. 3-thienylmagnesium
  42416. 3.1.0
  42417. 3.2.0
  42418. 3.2.1
  42419. 3.2.1.0
  42420. 3.2.2
  42421. 3.3.0
  42422. 3.3.1
  42423. 30-95
  42424. 32-82
  42425. 32-93
  42426. 34-89
  42427. 34-98
  42428. 34-anti
  42429. 34-syn-mismatched
  42430. 35-87
  42431. 35-95
  42432. 36-79
  42433. 39-72
  42434. 39:61
  42435. butyldimethylsilylox
  42436. ethyl
  42437. carboxyethyl
  42438. other
  42439. examples
  42440. 86-96
  42441. 71-86
  42442. other
  42443. examples
  42444. 51-90
  42445. other
  42446. examples
  42447. 60-84
  42448. yield
  42449. other
  42450. examples
  42451. 65-89
  42452. yield
  42453. ratios
  42454. 42:58
  42455. 100:0
  42456. other
  42457. examples
  42458. 75-90
  42459. yield
  42460. other
  42461. examples
  42462. 80-98
  42463. yield
  42464. other
  42465. examples
  42466. 83-91
  42467. yields
  42468. other
  42469. examples
  42470. 89-92
  42471. 73-81
  42472. other
  42473. examples
  42474. clean
  42475. inversion
  42476. phenylpentacyclo
  42477. 5.3.0.0
  42478. decan
  42479. onein
  42480. acetic
  42481. 4-methoxyaniline
  42482. 4-methoxyaniline
  42483. 4.1.0
  42484. 4.1.0.0
  42485. 4.2.0
  42486. 4.2.0.0
  42487. 4.3.0
  42488. 4.3.1.1
  42489. 40-80
  42490. 40-85
  42491. 41-71
  42492. 41-87
  42493. 41/59
  42494. 42-97
  42495. 42:58
  42496. dimethylbenzo
  42497. difuran
  42498. highly
  42499. reactive
  42500. 45-75
  42501. 45-85
  42502. 45-90
  42503. 45-92
  42504. 45-96
  42505. 46-74
  42506. 464003
  42507. 48-70
  42508. 49-78
  42509. 49467
  42510. examples
  42511. 61-92
  42512. stable
  42513. formaldehyde
  42514. examples
  42515. furanone
  42516. synthesis
  42517. electrophilc
  42518. other
  42519. cyclization
  42520. examples
  42521. 74-85
  42522. yield
  42523. 6.2:1
  42524. other
  42525. examples
  42526. yields
  42527. other
  42528. examples
  42529. 50-80
  42530. overall
  42531. yields
  42532. other
  42533. examples
  42534. 50-90
  42535. 76:24
  42536. other
  42537. examples
  42538. 60-65
  42539. yield
  42540. 90-98
  42541. other
  42542. examples
  42543. 62-67
  42544. yield
  42545. other
  42546. examples
  42547. 63-85
  42548. yield
  42549. 81-99
  42550. other
  42551. examples
  42552. 67-81
  42553. yield
  42554. other
  42555. examples
  42556. 75-95
  42557. yield
  42558. other
  42559. examples
  42560. 97-100
  42561. yield
  42562. other
  42563. examples
  42564. yields
  42565. 66-82
  42566. selectivities
  42567. reduction
  42568. products
  42569. isolated
  42570. 5-tert-butyl-4-hydro
  42571. 5.0.5.4
  42572. 5.2.1.0
  42573. 5.3.0.0
  42574. 5.3.1.1
  42575. 50-73
  42576. 50-80
  42577. 50-85
  42578. 50-90
  42579. 51-77
  42580. 51-79
  42581. 51-90
  42582. 52:48
  42583. 53-86
  42584. 53-99
  42585. 55-90
  42586. 55-95
  42587. yield
  42588. 5791113
  42589. 58-98
  42590. 591317
  42591. 5a/5d/5b/5c
  42592. 5diastereomeric
  42593. cyclopropylidene
  42594. hexynes
  42595. prepared
  42596. palladi
  42597. examples
  42598. under
  42599. various
  42600. conditions
  42601. 9-100
  42602. yield
  42603. other
  42604. examples
  42605. yield
  42606. syn/anti
  42607. 1.5:1
  42608. other
  42609. examples
  42610. 41-87
  42611. chlorovinyl
  42612. alcohols
  42613. 19-77
  42614. other
  42615. examples
  42616. 50-85
  42617. other
  42618. examples
  42619. 60-76
  42620. isomeric
  42621. purity
  42622. other
  42623. examples
  42624. 74-97
  42625. yield
  42626. other
  42627. examples
  42628. 77-90
  42629. yield
  42630. other
  42631. examples
  42632. 87-95
  42633. 6-100
  42634. 6-endo
  42635. 6-endo
  42636. cyclization
  42637. 6.2:1
  42638. cyclization
  42639. products
  42640. reduction
  42641. product
  42642. 60-65
  42643. 60-76
  42644. 60-84
  42645. 60-91
  42646. 60:40
  42647. 61-92
  42648. 61-93
  42649. 62-100
  42650. 62-67
  42651. 62-88
  42652. 62-94
  42653. 62-98
  42654. 63-85
  42655. 63-90
  42656. 63-91
  42657. 63-95
  42658. 64-89
  42659. 64-93
  42660. 65-89
  42661. 65:35
  42662. 68-82
  42663. 68-92
  42664. 68-95
  42665. 68-98
  42666. 6a-epipretazettine
  42667. ketones
  42668. other
  42669. examples
  42670. other
  42671. examples
  42672. 23-85
  42673. yield
  42674. other
  42675. examples
  42676. 39-72
  42677. yields
  42678. other
  42679. examples
  42680. 43-85
  42681. yield
  42682. other
  42683. examples
  42684. 70-95
  42685. yield
  42686. other
  42687. examples
  42688. 70-99
  42689. yields
  42690. other
  42691. examples
  42692. 72-99
  42693. yields
  42694. other
  42695. examples
  42696. yield
  42697. other
  42698. examples
  42699. 84-91
  42700. generally
  42701. selectivity
  42702. other
  42703. examples
  42704. yield
  42705. describes
  42706. reactivity
  42707. variet
  42708. other
  42709. examples
  42710. 90-98
  42711. 95-98
  42712. 7.5/1
  42713. 70-100
  42714. 70-90
  42715. 70-92
  42716. 70-94
  42717. 70-95
  42718. 70-97
  42719. 70-99
  42720. 71-100
  42721. 71-86
  42722. 71-97
  42723. 72-88
  42724. 72-91
  42725. 72-92
  42726. 72-99
  42727. 73-81
  42728. 73-92
  42729. 74-85
  42730. 74-88
  42731. 74-97
  42732. 75-90
  42733. 75-95
  42734. 75-99
  42735. 76-93
  42736. 76/24
  42737. 76:24
  42738. 77-100
  42739. 77-90
  42740. 79-90
  42741. examples
  42742. 51-77
  42743. examples
  42744. resulting
  42745. bromolactonization
  42746. examples
  42747. 71-100
  42748. other
  42749. examples
  42750. other
  42751. examples
  42752. 45-90
  42753. yields
  42754. other
  42755. examples
  42756. 6-100
  42757. other
  42758. examples
  42759. 72-92
  42760. other
  42761. examples
  42762. 80-91
  42763. yield
  42764. 80-86
  42765. 80-90
  42766. 80-91
  42767. 80-94
  42768. 80-98
  42769. 80:20
  42770. 81-99
  42771. 810121416
  42772. 82:18
  42773. yield
  42774. 83-91
  42775. 84-91
  42776. 86-96
  42777. 86:12
  42778. 87-95
  42779. 87.5/12.5
  42780. 89-92
  42781. 89-98
  42782. 89:11
  42783. 89:11-98:2
  42784. examples
  42785. 35-87
  42786. examples
  42787. 50-73
  42788. yield
  42789. examples
  42790. 68-95
  42791. overall
  42792. yield
  42793. towards
  42794. total
  42795. synthesis
  42796. examples
  42797. 90-97
  42798. yield
  42799. 52:48
  42800. epimeric
  42801. ratios
  42802. examples
  42803. asymmetric
  42804. claisen
  42805. rearrangement
  42806. 22-99
  42807. examples
  42808. yields
  42809. 58-98
  42810. 73-92
  42811. other
  42812. examples
  42813. yield
  42814. other
  42815. examples
  42816. 49-78
  42817. yield
  42818. other
  42819. examples
  42820. 52-82
  42821. yield
  42822. other
  42823. examples
  42824. 53-86
  42825. other
  42826. examples
  42827. 68-98
  42828. yield
  42829. selectivity
  42830. other
  42831. examples
  42832. yield
  42833. other
  42834. examples
  42835. 70-100
  42836. 9-100
  42837. 90-97
  42838. 90-98
  42839. 90-98
  42840. product
  42841. formed
  42842. structure
  42843. chiral
  42844. 92-98
  42845. 92.5/7.5
  42846. 93:7-3:99
  42847. asymmetric
  42848. induction
  42849. yield
  42850. after
  42851. removal
  42852. treatment
  42853. water
  42854. selectivity
  42855. 9carbonyl
  42856. conceptually
  42857. attractive
  42858. enantioselective
  42859. synthesis
  42860. conditions
  42861. optimized
  42862. using
  42863. substrate
  42864. shown
  42865. above
  42866. convergent
  42867. synthesis
  42868. camptothecin
  42869. described
  42870. detailed
  42871. study
  42872. reactions
  42873. several
  42874. ketones
  42875. diastereoselective
  42876. addition
  42877. grignard
  42878. reagents
  42879. nonrac
  42880. direct
  42881. evidence
  42882. influence
  42883. aggregation
  42884. state
  42885. first
  42886. example
  42887. asymmetric
  42888. reduction
  42889. using
  42890. chiral
  42891. paper
  42892. ctive
  42893. reduction
  42894. epoxy
  42895. allylic
  42896. alcohols
  42897. iodoalkyl
  42898. ylides
  42899. prepared
  42900. first
  42901. kinetic
  42902. study
  42903. uncatalyzed
  42904. methanolysis
  42905. furyl
  42906. lithio
  42907. pyrrolidine
  42908. formamidine
  42909. derivativ
  42910. mechanistic
  42911. study
  42912. mukaiyama
  42913. aldol
  42914. addition
  42915. reaction
  42916. methoxy
  42917. acrylonitriles
  42918. available
  42919. aldehydes
  42920. ketone
  42921. method
  42922. selective
  42923. cleavage
  42924. tetrahydropyranyl
  42925. molecular
  42926. mechanics
  42927. model
  42928. transition
  42929. state
  42930. versatile
  42931. synthesis
  42932. tetracyclic
  42933. compounds
  42934. approach
  42935. asymmetric
  42936. construction
  42937. pyrrolo
  42938. chiral
  42939. building
  42940. block
  42941. hydroxy
  42942. gamma
  42943. trimethylsily
  42944. chiral
  42945. butenolide
  42946. synthons
  42947. starting
  42948. iodol
  42949. hydroborating
  42950. agent
  42951. isopropylapo
  42952. isopinocampheylbora
  42953. method
  42954. developed
  42955. synthesis
  42956. aromatic
  42957. heterot
  42958. methodology
  42959. allowing
  42960. assemble
  42961. fused
  42962. vinylcyclopropa
  42963. palladium
  42964. catalyzed
  42965. synthesis
  42966. alkylcoumarins
  42967. palladium
  42968. mediated
  42969. tandem
  42970. cyclization
  42971. carbonylation
  42972. procedure
  42973. synthesis
  42974. bromoalkynes
  42975. dmso/
  42976. route
  42977. asymmetric
  42978. sugar
  42979. analogs
  42980. starting
  42981. route
  42982. semisynthetic
  42983. docetaxel
  42984. described
  42985. using
  42986. synthesis
  42987. amino
  42988. hydroxy
  42989. carboxyanhydride
  42990. synthesis
  42991. diamino
  42992. hydroxyacids
  42993. through
  42994. optica
  42995. synthesis
  42996. symmetric
  42997. porphyrins
  42998. presented
  42999. synthesis
  43000. thiols
  43001. yield
  43002. utilizing
  43003. carbon
  43004. synthetic
  43005. route
  43006. towards
  43007. planar
  43008. disubstituted
  43009. benzo
  43010. total
  43011. synthesis
  43012. alpha
  43013. himachalene
  43014. sesquiterpne
  43015. novel
  43016. efficient
  43017. stereoselective
  43018. synthesis
  43019. perhy
  43020. novel
  43021. synthesis
  43022. dibenzobicyclo
  43023. 3.2.2
  43024. nonane
  43025. systems
  43026. novel
  43027. technique
  43028. efficient
  43029. synthesis
  43030. fused
  43031. nitro
  43032. number
  43033. lewis
  43034. acids
  43035. examined
  43036. ticl4
  43037. andet2alcl
  43038. synthesis
  43039. acylaziridines
  43040. carboxylic
  43041. overman
  43042. paper
  43043. describesboth
  43044. inter
  43045. intramolecular
  43046. palladium
  43047. catalytic
  43048. recently
  43049. reported
  43050. modified
  43051. hantzsch
  43052. reaction
  43053. reinvesti
  43054. review
  43055. chemistry
  43056. biology
  43057. taxol
  43058. nicolaou
  43059. angew
  43060. sequence
  43061. generating
  43062. dolabellane
  43063. diterpene
  43064. framewor
  43065. series
  43066. nitro
  43067. phenyl
  43068. benzopyrans
  43069. series
  43070. hexenyllithiums
  43071. having
  43072. phenyl
  43073. trimethylsilyl
  43074. series
  43075. hexenyllithiums
  43076. having
  43077. phenyl
  43078. trimethylsilyl
  43079. series
  43080. cyclic
  43081. penta
  43082. heptapeptides
  43083. synthesi
  43084. series
  43085. isoxazoles
  43086. isoxazolines
  43087. synthesized
  43088. series
  43089. nitrones
  43090. joined
  43091. amides
  43092. olefins
  43093. series
  43094. palladium
  43095. catalysed
  43096. three
  43097. component
  43098. cyclisation
  43099. short
  43100. stereoselective
  43101. synthesis
  43102. dihydrosesamin
  43103. short
  43104. enantioselective
  43105. synthesis
  43106. diepicastanospermin
  43107. simple
  43108. general
  43109. procedure
  43110. hydration
  43111. unactivated
  43112. simple
  43113. highly
  43114. diastereoselective
  43115. synthesis
  43116. simple
  43117. procedure
  43118. preparation
  43119. stereoselecti
  43120. small
  43121. amount
  43122. alcohol
  43123. formed
  43124. reduction
  43125. stereoselective
  43126. synthesis
  43127. trifunctionalised
  43128. tetrahy
  43129. stereospecific
  43130. synthesis
  43131. difunctionalised
  43132. tetrahydro
  43133. stoichiometric
  43134. amount
  43135. chiral
  43136. borane
  43137. turned
  43138. synthesis
  43139. alkenyl
  43140. alkyl
  43141. butadiene
  43142. synthetic
  43143. sequence
  43144. preparation
  43145. disubstitute
  43146. systematic
  43147. study
  43148. utility
  43149. readily
  43150. taxol
  43151. synthon
  43152. obtained
  43153. oxidative
  43154. cyclization
  43155. cyclopropaneproduct
  43156. undergoes
  43157. sigmatropic
  43158. transition
  43159. metal
  43160. mediated
  43161. acetylene
  43162. vinylidene
  43163. rearrangeme
  43164. reagent
  43165. nucleophilic
  43166. iodine
  43167. donor
  43168. variety
  43169. gamma
  43170. lactams
  43171. obtained
  43172. suitable
  43173. variety
  43174. reducing
  43175. agents
  43176. explored
  43177. effect
  43178. stereose
  43179. x-ray
  43180. structure
  43181. sparteine
  43182. lithiobutylindenide
  43183. complex
  43184. a-alkoxyimines
  43185. a-aminolithium
  43186. a-aminolithium
  43187. species
  43188. stable
  43189. presence
  43190. a-benzyloxy
  43191. abnormal
  43192. abounds
  43193. about
  43194. above
  43195. absence
  43196. absolute
  43197. abstraction
  43198. academic
  43199. academic
  43200. academic
  43201. press
  43202. accelerated
  43203. accelerates
  43204. acceleration
  43205. accepting
  43206. acceptor
  43207. accepts
  43208. access
  43209. accessible
  43210. accompanied
  43211. accomplished
  43212. accord
  43213. accordance
  43214. according
  43215. accounted
  43216. accounts
  43217. acene
  43218. acetal
  43219. acetaldehyde
  43220. acetalization
  43221. acetals
  43222. acetamide
  43223. acetanilides
  43224. acetate
  43225. acetates
  43226. acetic
  43227. acetone
  43228. acetonide
  43229. acetonides
  43230. acetonitrile
  43231. acetonyl
  43232. acetophenone
  43233. acetoxyketones
  43234. acetyl
  43235. acetylacetone
  43236. acetylation
  43237. acetylene
  43238. acetylenedicarboxyla
  43239. acetylenes
  43240. acetylenic
  43241. acetylides
  43242. achieve
  43243. achieved
  43244. achieves
  43245. achieves
  43246. achieving
  43247. achiral
  43248. achiral
  43249. enolates
  43250. preferentially
  43251. afford
  43252. aldol
  43253. catalyzed
  43254. equilibration
  43255. spiroketals
  43256. mediated
  43257. cyclization
  43258. reactions
  43259. described
  43260. seven
  43261. treatment
  43262. alpha
  43263. hydroxy
  43264. acetals
  43265. induced
  43266. alkyl
  43267. acidic
  43268. acidity
  43269. acidnature
  43270. acids
  43271. acidsaminoisobutyric
  43272. across
  43273. acrylate
  43274. acrylonitrile
  43275. acrylonitriles
  43276. acryloyl
  43277. action
  43278. activate
  43279. activate
  43280. amide
  43281. first
  43282. phosphorus
  43283. oxychloride
  43284. triphosgene
  43285. activated
  43286. activating
  43287. activation
  43288. active
  43289. activities
  43290. activity
  43291. actual
  43292. acyclic
  43293. chlorides
  43294. unaffected
  43295. generation
  43296. cp2tic
  43297. halides
  43298. adjacent
  43299. diene
  43300. group
  43301. react
  43302. acylaminol
  43303. acylated
  43304. acylating
  43305. acylation
  43306. acylchlorides
  43307. acyliminium
  43308. acylindoles
  43309. adamantan
  43310. adamantane
  43311. adamantanes
  43312. adamantone
  43313. added
  43314. addition
  43315. carbon
  43316. nucleophiles
  43317. cyclic
  43318. acyliminium
  43319. addition
  43320. chlorosulfonylisocya
  43321. heterocycles
  43322. addition
  43323. t-butyl
  43324. ammonium
  43325. second
  43326. catalyst
  43327. demon
  43328. addition
  43329. tricthylamine
  43330. mixture
  43331. pyridylthioester
  43332. additional
  43333. additionof
  43334. additions
  43335. additive
  43336. additives
  43337. addtion
  43338. adduct
  43339. adducts
  43340. adequate
  43341. adjacent
  43342. advanced
  43343. advantage
  43344. affected
  43345. affinity
  43346. afford
  43347. afford
  43348. afforded
  43349. affording
  43350. affords
  43351. aflash
  43352. after
  43353. again
  43354. against
  43355. agclo4
  43356. agency
  43357. agent
  43358. ratio
  43359. products
  43360. agreement
  43361. akademiai
  43362. akademiai
  43363. kiado
  43364. alcohlos
  43365. alcohol
  43366. alcohols
  43367. afford
  43368. agents@
  43369. alcohols
  43370. aldehydes@
  43371. alkali@
  43372. alkenylated@
  43373. alkylating
  43374. allows@
  43375. allylboration@
  43376. alpha
  43377. chtoroalkylidene
  43378. gamma
  43379. butyrolactone
  43380. acet@
  43381. jorgensen
  43382. control
  43383. diastereo
  43384. synlett
  43385. lanthanide
  43386. bis-trifluoromethane
  43387. alstonia@
  43388. aminoacid@
  43389. addition
  43390. benzaldehyde
  43391. ethereal
  43392. solution
  43393. extremely
  43394. convenient
  43395. deoxygenation
  43396. alkenyl
  43397. alkyl
  43398. analog@
  43399. and/or@
  43400. another@
  43401. elimination
  43402. appropriately@
  43403. aromatic
  43404. oximes
  43405. obtained
  43406. stereospecifically
  43407. action
  43408. aryl/heteroaryl@
  43409. little
  43410. molar
  43411. equivalent
  43412. elemental
  43413. tellurium
  43414. asymmetry@
  43415. attacks@
  43416. available
  43417. avoid@
  43418. participating
  43419. compounds
  43420. configuration
  43421. contracted
  43422. alcohols
  43423. aldehyde
  43424. aldehydes
  43425. ketones
  43426. converted
  43427. alpha
  43428. hydroxystan
  43429. aldehydes
  43430. undergo
  43431. efficient
  43432. stereoselective
  43433. horner
  43434. aldehydes
  43435. secondary
  43436. tertiary
  43437. carbon
  43438. aldehyes
  43439. alder
  43440. aldimines
  43441. aldofuranose
  43442. aldol
  43443. aldol
  43444. reactions
  43445. sodium
  43446. enolates
  43447. alpha
  43448. dibenzyl
  43449. aldoladducts
  43450. aldolate
  43451. aldols
  43452. aldopyranose
  43453. aldoximes
  43454. aliphatic
  43455. alkali
  43456. alkaloid
  43457. alkaloids
  43458. alkanethiols
  43459. alken
  43460. alkene
  43461. alkenes
  43462. alkenes
  43463. include
  43464. chcome
  43465. chco2me
  43466. alkenes
  43467. synthesised
  43468. alpha
  43469. bromobenzyl
  43470. benzyldiph
  43471. alkenoic
  43472. alkenoyl
  43473. alkenyl
  43474. alkenyl-zrcp2cl
  43475. kenylstannanes
  43476. alkenyltrimethylstan
  43477. alkoxide
  43478. alkoxides
  43479. alkoxy
  43480. alkoxyalkyl
  43481. alkoxycarbonyl
  43482. alkoxycarbonyloxyl
  43483. alkoxycyclohexadieno
  43484. alkoxyester
  43485. alkoxytricyclo
  43486. alkoxytrimethylsilan
  43487. alkyl
  43488. alkylate
  43489. alkylated
  43490. alkylating
  43491. alkylating
  43492. alkylation
  43493. alkylation
  43494. sulfone
  43495. anion
  43496. attempted
  43497. alkylations
  43498. alkylative
  43499. alkylcoumarins
  43500. alkyliden
  43501. alkylidene
  43502. alkylidenecyclopenta
  43503. alkylidenethiophenes
  43504. alkyllithium
  43505. alkyllithiums
  43506. alkylthioethylenic
  43507. alkylthionitroso
  43508. alkyn
  43509. alkyne
  43510. alkyne-co2
  43511. alkynes
  43512. alkynoates
  43513. alkynyl
  43514. allene
  43515. allenes
  43516. allenic
  43517. allenones
  43518. allenyl
  43519. allow
  43520. allowed
  43521. allowing
  43522. allyl/benzyl
  43523. allylate
  43524. allylation
  43525. allylboration
  43526. allylester
  43527. allylic
  43528. allylic
  43529. homallylic
  43530. alkoxycarbonyloxyl
  43531. radicals
  43532. produced
  43533. allylketene
  43534. allyloxyacetaldehyde
  43535. allyloxymethyl
  43536. allyloxypropargyl
  43537. allylpalladium
  43538. allylsilanes
  43539. allyltrimethylsilane
  43540. allylzirconation
  43541. almost
  43542. along
  43543. alpha
  43544. alpha
  43545. heteroatom
  43546. substituted
  43547. orthoesters
  43548. prepared
  43549. andfo
  43550. alpha
  43551. hydroxy
  43552. acids
  43553. reacted
  43554. dihydropyrans
  43555. alpha
  43556. iodos
  43557. delta
  43558. gamma
  43559. hexonolactones
  43560. alpha
  43561. alpha
  43562. silyl
  43563. alpha
  43564. substituted
  43565. acetic
  43566. esters
  43567. prepar
  43568. alpha
  43569. chtoroalkylidene
  43570. gamma
  43571. butyrolactone
  43572. alpine
  43573. cyclopentanone
  43574. cyclopropanone
  43575. describes
  43576. method
  43577. using
  43578. glycol
  43579. ester
  43580. ethanolamine
  43581. similar
  43582. results
  43583. methylenation
  43584. ketones
  43585. model
  43586. system
  43587. studied
  43588. noteworthy
  43589. reduction
  43590. conversion
  43591. epoxide
  43592. fallis
  43593. barrett
  43594. total
  43595. synthesis
  43596. papuamin
  43597. issue
  43598. pyridine
  43599. alstonia
  43600. altering
  43601. alternative
  43602. alternatively
  43603. although
  43604. although
  43605. previous
  43606. studies
  43607. shown
  43608. ocyclic
  43609. gamma
  43610. alumina/dmap
  43611. aluminum
  43612. always
  43613. malgam
  43614. ambient
  43615. ambruticine
  43616. chemical
  43617. american
  43618. american
  43619. chemical
  43620. society
  43621. american
  43622. chemical
  43623. society
  43624. washington
  43625. amide
  43626. amides
  43627. amidoketones
  43628. amidyl
  43629. amine
  43630. amineare
  43631. amines
  43632. amino
  43633. aminoacetylenes
  43634. aminoacid
  43635. aminoacids
  43636. aminoalcohol
  43637. aminoaldehyde
  43638. aminoaziridinylhydra
  43639. aminoazoles
  43640. aminobenzamides
  43641. aminobutanoic
  43642. aminochromenone
  43643. aminoether
  43644. aminoethyl
  43645. aminoisobutyric
  43646. aminomethyl
  43647. aminonitriles
  43648. aminoorganolithiums
  43649. aminostannane
  43650. ammmonium
  43651. ammonium
  43652. among
  43653. amount
  43654. amounts
  43655. thereal
  43656. solution
  43657. practical
  43658. synthesis
  43659. 246810
  43660. dodecapentae
  43661. efficient
  43662. enantioselective
  43663. method
  43664. preparation
  43665. efficient
  43666. catalytic
  43667. enantioselective
  43668. synthesis
  43669. efficient
  43670. catalyzed
  43671. oxidation
  43672. ketohydrazones
  43673. efficient
  43674. catalysed
  43675. acyliminium
  43676. cyclisati
  43677. efficient
  43678. excision
  43679. bridge
  43680. present
  43681. tricyclo
  43682. efficient
  43683. stereoselective
  43684. route
  43685. polyhydroxy
  43686. amino
  43687. efficient
  43688. synthesis
  43689. haloesters
  43690. achieved
  43691. efficient
  43692. three
  43693. synthesis
  43694. amino
  43695. efficient
  43696. tmsotf
  43697. catalyzed
  43698. ether
  43699. synthesis
  43700. carbonyl
  43701. expedient
  43702. general
  43703. method
  43704. synthesis
  43705. alkyl
  43706. extremely
  43707. convenient
  43708. deoxygenation
  43709. alkenyl
  43710. alkyl
  43711. intramolecular
  43712. diels
  43713. alder
  43714. cycloaddition
  43715. ketenimin
  43716. alkylation
  43717. study
  43718. pyridone
  43719. various
  43720. alcoho
  43721. study
  43722. lithio
  43723. dithiane
  43724. triorganosilyl
  43725. optically
  43726. advanced
  43727. intermediate
  43728. quassinoids
  43729. ultraviolet
  43730. photochemical
  43731. rearrangem
  43732. analogues
  43733. analyse
  43734. analysis
  43735. analyzed
  43736. anchimeric
  43737. anhydride
  43738. anilides
  43739. aniline
  43740. anilines
  43741. anion
  43742. anionic
  43743. anions
  43744. anisaldehyde
  43745. annulation
  43746. another
  43747. antagonists
  43748. anthraquinones
  43749. anthrarufin
  43750. anthrone
  43751. anthrone
  43752. found
  43753. react
  43754. methylmaleimide
  43755. ation
  43756. anti-felkin
  43757. anti/syn
  43758. antibiotic
  43759. antibiotics
  43760. antidepressant
  43761. antifeeding
  43762. antifungal
  43763. antiperiplanar
  43764. antispasmodic
  43765. antistereoselectivit
  43766. antitumor
  43767. apalladium
  43768. apoisopino
  43769. appeared
  43770. appears
  43771. applicable
  43772. application
  43773. applied
  43774. apply
  43775. approach
  43776. approaches
  43777. appropriate
  43778. appropriately
  43779. approx
  43780. approximately
  43781. aprocess
  43782. aqueous
  43783. group
  43784. pyridyl
  43785. quinoline
  43786. isoquinoline
  43787. derivatives
  43788. aracemic
  43789. arecapable
  43790. arenes
  43791. arenesulfonylhydrazo
  43792. aresult
  43793. aretrans
  43794. argon
  43795. arise
  43796. arising
  43797. aromatic
  43798. aromatic
  43799. aldehydes
  43800. react
  43801. sulfonium
  43802. salts
  43803. cyclic
  43804. aromatic
  43805. oximes
  43806. obtained
  43807. stereospecifically
  43808. action
  43809. aromatization
  43810. aromatized
  43811. aroyl
  43812. article
  43813. oaryl
  43814. arylation
  43815. arylboronic
  43816. arylcycloalkanes
  43817. arylcycloalkanes
  43818. produced
  43819. omega
  43820. alkenyl
  43821. benzylselen
  43822. arylethanolamines
  43823. arylethylamines
  43824. arylglycoside
  43825. arylhalides
  43826. arylisoquinolinium
  43827. aryloxy
  43828. aryloxyl
  43829. arylpropanoates
  43830. arylpyridines
  43831. arylsulfonyl
  43832. arylthio
  43833. arylthiols
  43834. arylthionitroso
  43835. alent
  43836. elemental
  43837. tellurium
  43838. asequence
  43839. asingle
  43840. asmall
  43841. aspartate
  43842. aspartic
  43843. assemble
  43844. assigned
  43845. assignement
  43846. assignment
  43847. assistance
  43848. assisted
  43849. assisting
  43850. association
  43851. assumed
  43852. assuming
  43853. asthe
  43854. asymetric
  43855. asymetric
  43856. dipolar
  43857. cycloaddition
  43858. nitrones
  43859. ketene
  43860. asymmetric
  43861. asymmetric
  43862. borane
  43863. reduction
  43864. alpha
  43865. ketoimines
  43866. oxazabo
  43867. asymmetric
  43868. dihydroxylation
  43869. primary
  43870. allylic
  43871. halides
  43872. asymmetricinduction
  43873. asymmetry
  43874. asynchronous
  43875. dianion
  43876. formed
  43877. which
  43878. warming
  43879. atertiary
  43880. athydroxylic
  43881. atmosphere
  43882. atmospheric
  43883. atoms
  43884. attachment
  43885. attack
  43886. attractive
  43887. attributed
  43888. authors
  43889. auxiliaries
  43890. auxiliary
  43891. auxilliary
  43892. availability
  43893. available
  43894. available
  43895. avaluable
  43896. average
  43897. oiding
  43898. avoids
  43899. axial
  43900. axially
  43901. azaallyl
  43902. azabicyclo
  43903. azabicycloheptenone
  43904. azadiene
  43905. azaenolate
  43906. azaindolinone
  43907. azaindolinones
  43908. azepin
  43909. azetidimone
  43910. azetidin
  43911. azetidinone
  43912. azide
  43913. azides
  43914. azidioiodinane
  43915. azido
  43916. azidoaldehyde
  43917. azidobenzonitriles
  43918. azine
  43919. azines
  43920. aziridine
  43921. aziridines
  43922. aziridinylhydrazones
  43923. azirines
  43924. azomethine
  43925. azulenone
  43926. b-keto
  43927. b-otbs
  43928. b-stannyl
  43929. b-stereocentre
  43930. babiak
  43931. baccatiniii
  43932. backlund
  43933. baeyer
  43934. bafilomycin
  43935. barbier
  43936. barrett
  43937. barrier
  43938. bartan
  43939. barton
  43940. et2nh
  43941. meona
  43942. piperidine
  43943. diisopropylamine
  43944. cases
  43945. based
  43946. bases
  43947. basic
  43948. basic
  43949. intramolecular
  43950. opening
  43951. reactions
  43952. vicinally
  43953. basis
  43954. bears
  43955. beating
  43956. because
  43957. become
  43958. becomes
  43959. beeni
  43960. beenprepared
  43961. beetle
  43962. before
  43963. behaviour
  43964. being
  43965. believed
  43966. below
  43967. benchtop
  43968. benzaldehyde
  43969. benzaldehydes
  43970. benzamide
  43971. benzazepinium
  43972. benzazocine
  43973. benzene
  43974. benzenedimethanol
  43975. benzeneseleninic
  43976. benzenesulfonyl
  43977. benzenethiol
  43978. benzimidazole
  43979. benzo
  43980. benzoate
  43981. benzodioxane
  43982. benzodithiin
  43983. benzofuran
  43984. benzopentalene
  43985. benzophenone
  43986. benzopyran
  43987. benzopyrano
  43988. benzopyranopyrazole
  43989. benzopyrans
  43990. benzoquinone
  43991. benzothiazines
  43992. benzothiopyran
  43993. benzotiazole
  43994. benzotiazole
  43995. functions
  43996. anion
  43997. stabilizing
  43998. group
  43999. benzotriazolylvi
  44000. benzotriazolylvinyl
  44001. benzoxazolinate
  44002. benzoyl
  44003. benzoylation
  44004. benzyl
  44005. benzylamine
  44006. benzylamine
  44007. benzylamine/ticl4
  44008. benzylated
  44009. benzylation
  44010. benzylazabicyclo
  44011. benzylazetidin
  44012. benzyldiphenylphosph
  44013. benzylic
  44014. benzylideneacetone
  44015. benzylidenepyruvate
  44016. benzyloxy
  44017. benzyloxypropyllithi
  44018. benzylselenides
  44019. benzyltetracyclic
  44020. benzyltrichloroimida
  44021. berlin
  44022. besides
  44023. allenic
  44024. hydrazones
  44025. undergo
  44026. hydrostannylation
  44027. afford
  44028. fluoropyrrole
  44029. derivatives
  44030. synthesized
  44031. yield
  44032. better
  44033. between
  44034. biaryl
  44035. biaryls
  44036. biased
  44037. bicarbonate
  44038. bicycle
  44039. bicyclic
  44040. bicycliclactones
  44041. bicyclo
  44042. bicyclobutonium
  44043. bicycloheptanes
  44044. bidentate
  44045. bidentate
  44046. bonding
  44047. olefinic
  44048. plays
  44049. impor
  44050. billington
  44051. binap
  44052. binaphthol
  44053. binaphthyl
  44054. binding
  44055. binol
  44056. biological
  44057. biologically
  44058. biology
  44059. biotin
  44060. biphenanthryl
  44061. biphenyl
  44062. biphenylene
  44063. biradical
  44064. bis-sulfoxide
  44065. bisadducts
  44066. bischler
  44067. bisdiene
  44068. bisenolate
  44069. bishomopropargylic
  44070. bislactim
  44071. bismetallic
  44072. bispalladium
  44073. bisphosphine
  44074. blackie
  44075. blackie
  44076. academic
  44077. professional
  44078. blackie
  44079. cademic
  44080. professional/chapman
  44081. blackie
  44082. blackwell
  44083. blackwell
  44084. scientific
  44085. publications
  44086. blastmycinolactol
  44087. block
  44088. blocks
  44089. protected
  44090. amino
  44091. aldehydes
  44092. derived
  44093. amino
  44094. bonded
  44095. bonding
  44096. bonds
  44097. books
  44098. borane
  44099. boranes
  44100. borobicyclo
  44101. borohydride
  44102. boron
  44103. boron
  44104. enolates
  44105. bearing
  44106. menthone
  44107. derived
  44108. chiral
  44109. ligands
  44110. areca
  44111. boron
  44112. enolates
  44113. derived
  44114. alpha
  44115. heterosubstituted
  44116. thioacet
  44117. boronates
  44118. boronic
  44119. 111333
  44120. hexamethyldisilazane
  44121. trimethylsilyl
  44122. hexonolactones
  44123. provide
  44124. templates
  44125. constr
  44126. starting
  44127. material
  44128. product
  44129. enantiomeric
  44130. purities
  44131. bound
  44132. bphenylthiyl
  44133. branched
  44134. breach
  44135. breaking
  44136. brevetoxin
  44137. bridge
  44138. bridges
  44139. briefly
  44140. bring
  44141. brinker
  44142. broadly
  44143. bromide
  44144. bromides
  44145. brominating
  44146. bromination
  44147. bromine
  44148. bromo
  44149. bromo/iodo
  44150. bromoacetanilides
  44151. bromoacetate
  44152. bromoalkynes
  44153. bromobenzyl
  44154. bromocyclohex
  44155. bromoesters
  44156. bromoetherification
  44157. bromolactonization
  44158. bromosuccinimide
  44159. benzotriazol-1-yl
  44160. bu3snchbr2
  44161. bu3snh
  44162. bu4ni
  44163. buffered
  44164. building
  44165. bulky
  44166. bulky
  44167. bureau
  44168. burgess
  44169. butadiene
  44170. butadienes
  44171. butadienyl
  44172. butadienylmalonates
  44173. butane
  44174. butanoic
  44175. butanol
  44176. buten
  44177. butene
  44178. butenolide
  44179. butenolides
  44180. butenyl
  44181. buthylthiolate
  44182. butoxycarbonyl
  44183. butterworths
  44184. butyl
  44185. butylammonium
  44186. butylbiphenyl
  44187. butyldimethylsiloxy
  44188. butyldimethylsilyl
  44189. butyldimethylsilyldi
  44190. butyldimethylsilylox
  44191. butyllithium
  44192. butylstannyl
  44193. butylthio
  44194. butyn
  44195. butyrolactone
  44196. byassuming
  44197. bydichlorodicyano
  44198. acetal
  44199. alkene
  44200. cyclizations
  44201. c4h9br
  44202. cademic
  44203. calculate
  44204. calculations
  44205. calicheamcin
  44206. calorimetry
  44207. calyculin
  44208. cambridge
  44209. cambridge
  44210. universit
  44211. press
  44212. cambridge
  44213. university
  44214. press
  44215. cambridge
  44216. university
  44217. press
  44218. cambridge
  44219. campheylboranes
  44220. camphor
  44221. camphorsulfonic
  44222. camptothecin
  44223. ulfur
  44224. cation
  44225. canalso
  44226. cannot
  44227. capable
  44228. capped
  44229. capture
  44230. captured
  44231. carbalkoxy
  44232. carbamates
  44233. carbamoyl
  44234. carbamyl
  44235. carbanion
  44236. carbanionic
  44237. carbanions
  44238. carbapenem
  44239. carbazole
  44240. carbene
  44241. carbenic
  44242. carbenoid
  44243. carbenoids
  44244. carbinyl
  44245. carbo
  44246. carbobicycles
  44247. carbobicyclic
  44248. carbocations
  44249. carbocycle
  44250. carbocycles
  44251. carbocyclic
  44252. carbocyclization
  44253. carbodiimides
  44254. carbohydrate
  44255. carbohydrates
  44256. carbohydrates
  44257. possessing
  44258. suitably
  44259. positioned
  44260. hydoxyl
  44261. group
  44262. carboline
  44263. carbolines
  44264. carbomethoxy
  44265. carbomethoxylation
  44266. carbon
  44267. carbon
  44268. carbon-carbon
  44269. carbonate
  44270. carbonates
  44271. carbonic
  44272. carbons
  44273. carbonyl
  44274. carbonylamino
  44275. carbonylated
  44276. carbonylation
  44277. carbonylationand
  44278. carbonylreduction
  44279. carbonyls
  44280. carboxaldehyde
  44281. carboxamido
  44282. carboxyanhydrides
  44283. carboxyethyl
  44284. carboxyl
  44285. carboxylate
  44286. carboxylates
  44287. carboxylic
  44288. carboxylic
  44289. acids
  44290. conveniently
  44291. esterfied
  44292. alcohols
  44293. carboxypyrazolines
  44294. carried
  44295. carry
  44296. carvone
  44297. cascade
  44298. atalyse
  44299. catalysed
  44300. catalysis
  44301. catalyst
  44302. stability
  44303. catalysts
  44304. catalytic
  44305. catalytic
  44306. amount
  44307. cobalt
  44308. chloride
  44309. dichloroethane
  44310. catalyze
  44311. catalyzed
  44312. catalyzes
  44313. catechol
  44314. catecholborane
  44315. cation
  44316. cationic
  44317. cations
  44318. cause
  44319. caused
  44320. causes
  44321. cecl3
  44322. cedar
  44323. cedrusdeodara
  44324. center
  44325. centers
  44326. central
  44327. centred
  44328. centres
  44329. centrosymmetric
  44330. cephalotaxine
  44331. cephalotaxinel
  44332. cephen
  44333. ceric
  44334. cerium
  44335. certain
  44336. cesium
  44337. cf3con
  44338. cf3sime3
  44339. ch2ch2
  44340. ch2ch2oh
  44341. ch2cl2
  44342. ch2i2
  44343. ch2oh
  44344. ch2znbr
  44345. ch3cn
  44346. chain
  44347. chains
  44348. chair
  44349. chair
  44350. nging
  44351. chapman
  44352. chapman
  44353. characterization
  44354. characterized
  44355. charge
  44356. charged
  44357. chcl3
  44358. chco2me
  44359. chcome
  44360. chelate
  44361. chelated
  44362. chelates
  44363. chelating
  44364. chelation
  44365. chelation
  44366. chelation-controlled
  44367. chemical
  44368. chemical
  44369. highlights
  44370. chemical
  44371. information
  44372. system
  44373. chemio
  44374. chemistry
  44375. chemo
  44376. ively
  44377. chemospecificity
  44378. chichester
  44379. chimica
  44380. chiral
  44381. chiral
  44382. diazo
  44383. methyl
  44384. ketone
  44385. successfully
  44386. converte
  44387. chiral
  44388. mikanecic
  44389. synthesized
  44390. enantiomeric
  44391. chirality
  44392. chirally
  44393. chloranil
  44394. chloride
  44395. chlorides
  44396. chlorimine
  44397. chlorine
  44398. chloro
  44399. chlorochroman
  44400. chloroform
  44401. chloroketenes
  44402. chloromethyl
  44403. chloropalladation
  44404. chloroperbenzoic
  44405. chloroperoxybenroic
  44406. chloroperoxybenzoic
  44407. chlorosulfenylchroma
  44408. chlorosulfonyl
  44409. chlorosulfonylamides
  44410. chlorosulfonylisocya
  44411. chlorothiadiazolone
  44412. chlorothioalkyl
  44413. chlorovinyl
  44414. choice
  44415. cholestan
  44416. choosing
  44417. chroman
  44418. chromia
  44419. chromium
  44420. chromone
  44421. chtoroalkylidene
  44422. cinchona
  44423. cinnamates
  44424. cinnamyl
  44425. chloro
  44426. dimethylimidazolidiu
  44427. hexafluorophosphate
  44428. epoxide
  44429. yield
  44430. cis-endo
  44431. cis-exo
  44432. cis-selectivity
  44433. cis-tetrahydropyran
  44434. claimed
  44435. claisen
  44436. clarendon
  44437. clarendon
  44438. press
  44439. classical
  44440. clco2et
  44441. clcooet
  44442. clean
  44443. cleanly
  44444. cleavage
  44445. cleavages
  44446. cleaveage
  44447. cleaved
  44448. cleaves
  44449. clock
  44450. closure
  44451. closures
  44452. co2et
  44453. co2me
  44454. cobalt
  44455. cocatalysts
  44456. cohen
  44457. combination
  44458. combination
  44459. neighboring
  44460. amino
  44461. group
  44462. participating
  44463. combined
  44464. commercially
  44465. commercially
  44466. available
  44467. copper
  44468. bromide
  44469. dimethyl
  44470. sulfide
  44471. common
  44472. commun
  44473. comparable
  44474. compared
  44475. compares
  44476. compares
  44477. methods
  44478. leusen
  44479. barton
  44480. compatible
  44481. compete
  44482. competing
  44483. competition
  44484. competitive
  44485. complementary
  44486. complementing
  44487. complete
  44488. complete
  44489. retention
  44490. configuration
  44491. evidense
  44492. against
  44493. radical
  44494. completed
  44495. completely
  44496. completes
  44497. completing
  44498. complex
  44499. component
  44500. components
  44501. composed
  44502. compound
  44503. compounds
  44504. compounds
  44505. comprehensive
  44506. comprising
  44507. computational
  44508. computational
  44509. paper
  44510. concentration
  44511. concentrations
  44512. concepts
  44513. conceptually
  44514. concerted
  44515. concertedreaction
  44516. concomitant
  44517. condensation
  44518. condensation
  44519. ketone
  44520. derived
  44521. nitrones
  44522. methylcarboxi
  44523. condensations
  44524. condensing
  44525. condition
  44526. conditions
  44527. dmf-thf
  44528. etni-pr2
  44529. conducted
  44530. confers
  44531. configurated
  44532. configuration
  44533. configuration
  44534. configurational
  44535. configurationally
  44536. configurations
  44537. configurationthis
  44538. confirmed
  44539. confirms
  44540. conformation
  44541. conformational
  44542. conformationaly
  44543. conformations
  44544. conformer
  44545. congested
  44546. conitions
  44547. conjugate
  44548. conjugate
  44549. addition
  44550. favoured
  44551. 12-addition
  44552. shieldin
  44553. conjugated
  44554. connected
  44555. consecutive
  44556. considerations
  44557. consistent
  44558. consists
  44559. constants
  44560. constituting
  44561. construct
  44562. consultants
  44563. consultants
  44564. bureau
  44565. contact
  44566. contained
  44567. containing
  44568. contains
  44569. contains
  44570. using
  44571. tbdms
  44572. triflate
  44573. context
  44574. continue
  44575. contracted
  44576. contracted
  44577. contraction
  44578. contrary
  44579. contrast
  44580. control
  44581. controlled
  44582. controlling
  44583. controls
  44584. convened
  44585. convenient
  44586. conveniently
  44587. convergent
  44588. conversion
  44589. converted
  44590. converts
  44591. coome
  44592. coordinate
  44593. coordinated
  44594. coordination
  44595. copper
  44596. copper
  44597. chloride
  44598. induced
  44599. chemo
  44600. regioselectivechlor
  44601. cordell
  44602. corey
  44603. correlated
  44604. corresponding
  44605. corresponding
  44606. correspondsto
  44607. corroborates
  44608. cortisone
  44609. could
  44610. coumarin
  44611. counterparts
  44612. couple
  44613. coupled
  44614. couples
  44615. coupling
  44616. coworkers
  44617. coxon
  44618. cp2ticl2
  44619. cr-pilc
  44620. cr-pilc
  44621. chromia
  44622. pillared
  44623. montmorillonite
  44624. catalyst
  44625. crafts
  44626. crassin
  44627. press
  44628. crcl2
  44629. creates
  44630. corresponding
  44631. couplings@
  44632. creates
  44633. cuprates@
  44634. cyclialkylation@
  44635. cyclization
  44636. radicals
  44637. derived
  44638. homolysis
  44639. cycloaddition
  44640. cycloaddition
  44641. reactions
  44642. between
  44643. various
  44644. vinyl
  44645. cyclopentane
  44646. d-aminoacid@
  44647. danishefsky's@
  44648. gruyter
  44649. demands@
  44650. deoxy@
  44651. derived
  44652. despite@
  44653. developed
  44654. diastereo@
  44655. diastereomers@
  44656. dibal-h@
  44657. dibenzyldiphenyl@
  44658. dieneophile@
  44659. dienoic
  44660. dihydroisocoumarin@
  44661. dimethylacetals@
  44662. dimethylhydrazone
  44663. direct
  44664. distort@
  44665. docetaxel@
  44666. olefin
  44667. gives
  44668. corresponding
  44669. isomer
  44670. ee's@
  44671. effects
  44672. electrophiles
  44673. either
  44674. iodine
  44675. quench@
  44676. electrophilic
  44677. eleven@
  44678. employing
  44679. pibatidine@
  44680. epoxides@
  44681. estergroups@
  44682. ethoxyvinyllithium@
  44683. example@
  44684. examples
  44685. creates
  44686. cross
  44687. crossover
  44688. crotonaldehyde
  44689. crotyl
  44690. crotylbromide
  44691. crown
  44692. crucial
  44693. crystal
  44694. crystalline
  44695. crystalline
  44696. lithiomethylene
  44697. tetramethylindan
  44698. forms
  44699. crystallization
  44700. crystallographic
  44701. crystallography
  44702. crystalstructures
  44703. cs2co3
  44704. cucl2
  44705. culminate
  44706. cuprate
  44707. curve
  44708. cyanide
  44709. cyano
  44710. cyanoamides
  44711. cyanoamine
  44712. cyanoamines
  44713. cyanoborohydride
  44714. cyanoformate
  44715. cyanohydrine
  44716. cyanohydrinsexhibiti
  44717. cyanomethylenetribut
  44718. cyanomethylenetribut
  44719. shown
  44720. mediate
  44721. direct
  44722. condens
  44723. cyclialkylation
  44724. cyclic
  44725. cyclic
  44726. membered
  44727. secondary
  44728. alpha
  44729. amino
  44730. acids
  44731. cyclicenone
  44732. cyclisation
  44733. cyclisation
  44734. carbomethoxylation
  44735. successfully
  44736. compete
  44737. cyclisations
  44738. cyclization
  44739. homolysis
  44740. cyclizations
  44741. cyclize
  44742. cyclized
  44743. cyclizes
  44744. cyclizing
  44745. cycloaddition
  44746. cycloaddition
  44747. addition
  44748. reactions
  44749. between
  44750. various
  44751. vinyl
  44752. cycloaddition
  44753. reactions
  44754. between
  44755. chiral
  44756. pyrone
  44757. derivati
  44758. cycloadditions
  44759. cycloadduct
  44760. cycloadducts
  44761. cycloalkane
  44762. cycloalkenes
  44763. cycloalkenyl
  44764. cycloalkyl
  44765. cycloalkylaldehydes
  44766. cyclobisalkylated
  44767. cyclobutanedione
  44768. cyclobutanol
  44769. cyclobutanone
  44770. cycloheptanones
  44771. cyclohex
  44772. cyclohexadiene
  44773. cyclohexane
  44774. cyclohexanol
  44775. cyclohexanone
  44776. cyclohexanones
  44777. cyclohexen
  44778. cyclohexene
  44779. cyclohexenonewith
  44780. cyclohexenyl
  44781. cycloisomerization
  44782. cyclopent
  44783. cyclopent
  44784. indene
  44785. benzopentalene
  44786. generated
  44787. flash
  44788. cyclopenta
  44789. cyclopentadiene
  44790. cyclopentadienes
  44791. cyclopentadienides
  44792. cyclopentane
  44793. cyclopentane
  44794. cyclopentanes
  44795. cyclopentanone
  44796. cyclopentanones
  44797. cyclopentapyranones
  44798. cyclopentene
  44799. cyclopentenyl
  44800. cyclopeptides
  44801. cyclopropanation
  44802. cyclopropane
  44803. cyclopropaneproduct
  44804. cyclopropanes
  44805. cyclopropanol
  44806. cyclopropanone
  44807. cycloproparenes
  44808. cycloproparenes
  44809. react
  44810. silver
  44811. chloroform
  44812. yield
  44813. cyclopropyl
  44814. cyclopropylacrylates
  44815. cyclopropylcarbinyl
  44816. cyclopropylcyclopent
  44817. cyclopropylidene
  44818. cyclopropylideneacet
  44819. cyclosilyl
  44820. cylic
  44821. cysteine
  44822. cytotoxic
  44823. evans
  44824. 1990112
  44825. tetrahedron
  44826. 199248
  44827. mannich
  44828. reactions
  44829. d-unsaturated
  44830. d3cobu
  44831. danishefsky
  44832. ruyter
  44833. camptothecin
  44834. intermediate
  44835. prepared
  44836. enantiosel
  44837. deacetylbaccatin
  44838. deactivates
  44839. dealing
  44840. deallyloxycarbonylat
  44841. decan
  44842. decanes
  44843. decapentaenoic
  44844. decarboxylation
  44845. decomplexation
  44846. decomposition
  44847. decompositions
  44848. decompostion
  44849. decrease
  44850. decreases
  44851. decreasing
  44852. decyanation
  44853. deethylibophyllidine
  44854. defined
  44855. definitively
  44856. degree
  44857. degrees
  44858. dehydration
  44859. dehydroacetylation
  44860. dehydrobromination
  44861. dehydrogenation
  44862. deips
  44863. dekker
  44864. delineated
  44865. delta
  44866. delta
  44867. acetylenic
  44868. metallated
  44869. propargylic
  44870. derivatives
  44871. undergo
  44872. demand
  44873. demands
  44874. demercuration
  44875. demonstrated
  44876. demonstratef
  44877. denmark
  44878. deoxygenated
  44879. deoxygenation
  44880. depend
  44881. dependence
  44882. dependent
  44883. depending
  44884. depends
  44885. deprotected
  44886. deprotection
  44887. deprotections
  44888. deprotonated
  44889. deprotonation
  44890. deprotonation
  44891. subsequent
  44892. silylation
  44893. allyl
  44894. phenyli
  44895. derivative
  44896. derivatives
  44897. derivatives
  44898. benzo
  44899. naphthyridine
  44900. prepared
  44901. derived
  44902. derived
  44903. deriving
  44904. desacetylbaccatin
  44905. describe
  44906. described
  44907. describes
  44908. describesboth
  44909. design
  44910. desired
  44911. etailed
  44912. details
  44913. detectable
  44914. detected
  44915. determinations
  44916. determine
  44917. determined
  44918. determining
  44919. detosylation
  44920. deuterated
  44921. deuteride
  44922. deuterium
  44923. deuterium
  44924. incorporation
  44925. observed
  44926. cd3od
  44927. developed
  44928. developed
  44929. developement
  44930. developements
  44931. development
  44932. devoted
  44933. diacetate
  44934. diacetoxyiodo
  44935. diacetyl
  44936. diacylimidazolidin
  44937. diacylimidazolidine
  44938. dialkoxyisoxazolidin
  44939. dialkyl
  44940. dialkylamide
  44941. dialkylamino
  44942. dialkylated
  44943. dialkylhydrazones
  44944. dialkylpiperidine
  44945. dialkylthioamide
  44946. dialkyltriazenes
  44947. diallyl
  44948. diallyldiazoacetamid
  44949. diamine
  44950. diamines
  44951. diamino
  44952. dianion
  44953. dianions
  44954. diaryl
  44955. diaryls
  44956. diastercomeric
  44957. diastereoface
  44958. diastereofacial
  44959. diastereofacially
  44960. diastereoisomer
  44961. diastereoisomeric
  44962. diastereoisomers
  44963. diastereomer
  44964. diastereomeric
  44965. diastereomerically
  44966. diastereomers
  44967. diastereoselection
  44968. diastereoselective
  44969. diastereoselectively
  44970. diastereoselectiviti
  44971. diastereoselectivity
  44972. diastereoselectivity
  44973. found
  44974. significantly
  44975. higher
  44976. diastero
  44977. diaza
  44978. diazepinederivative
  44979. diazo
  44980. diazoacetamides
  44981. diazoalkanes
  44982. diazodecomposition
  44983. diazodecomposition
  44984. butyl
  44985. buten
  44986. diazoaceta
  44987. diazoester
  44988. diazoesters
  44989. diazoethane
  44990. diazoketoester
  44991. diazoketones
  44992. diazomethane
  44993. diazomethanes
  44994. diazotization
  44995. diazotization
  44996. aminobenzamides
  44997. methanol
  44998. presen
  44999. dibal
  45000. dibalh
  45001. dibenzo
  45002. dibenzobicyclo
  45003. dibenzosuberyl
  45004. dibenzyl
  45005. dibenzylamino
  45006. dibenzyldiphenyl
  45007. dibenzylideneacetony
  45008. diboa
  45009. dibromo
  45010. dibromoalkenes
  45011. dibromoethane
  45012. dibromoethylenes
  45013. dibutyl
  45014. dibutylboron
  45015. dibutylboron
  45016. enolates
  45017. diacylimidazolidine
  45018. thiones
  45019. dicarbonyl
  45020. dicarboxylate
  45021. dicarboxylates
  45022. dichloride
  45023. dichloro
  45024. dichlorobut
  45025. dichlorochroman-4
  45026. dichlorodiethylsilan
  45027. dichloroethane
  45028. dichloroethenes
  45029. dichloroketene
  45030. dichloromethane
  45031. dicobalt
  45032. dicyanoanthracene
  45033. dicyanocyclopentadie
  45034. dicyclohexylsulfamoy
  45035. diels
  45036. diels
  45037. alder
  45038. reactions
  45039. quinolinetriones
  45040. comple
  45041. diels-alder
  45042. dienamines
  45043. diene
  45044. dienic
  45045. dienoate
  45046. dienoic
  45047. dienoic
  45048. dienol
  45049. dienone
  45050. dienophile
  45051. dienophiles
  45052. dienophiles
  45053. methyl
  45054. benzodithiin
  45055. tetroxide
  45056. pheny
  45057. dienophilic
  45058. dienyl
  45059. dienylic
  45060. dienyne
  45061. diepicastanospermine
  45062. diepoxides
  45063. diepoxy
  45064. diepoxybutane
  45065. diesters
  45066. diethoxybutyrate
  45067. diethoxypropionate
  45068. diethyl
  45069. diethylaluminum
  45070. diethylaluminum
  45071. azide
  45072. prepared
  45073. either
  45074. sodium
  45075. azide
  45076. diethylamine
  45077. diethylisopropylsily
  45078. diethylzinc
  45079. differ
  45080. different
  45081. differential
  45082. differently
  45083. differently
  45084. substituted
  45085. allylic
  45086. bromides
  45087. react
  45088. protec
  45089. differentnon
  45090. differentpyrimidones
  45091. differing
  45092. differs
  45093. difficult
  45094. difluoro
  45095. difunctionalised
  45096. difuran
  45097. dihaloalkanes
  45098. dihydro
  45099. dihydrofuran
  45100. dihydroisocoumarin
  45101. dihydronaphthalenes
  45102. dihydropyran
  45103. dihydropyrans
  45104. dihydropyridine
  45105. dihydropyridines
  45106. dihydroquinidinyl
  45107. dihydrosesamin
  45108. dihydroxyamides
  45109. dihydroxylation
  45110. diiodide
  45111. diisobutylaluminum
  45112. diisopropoxytitanium
  45113. diisopropylamine
  45114. diisopropylethylamin
  45115. diisopropylphosphino
  45116. diketone-type
  45117. diketones
  45118. dilithiated
  45119. dilithiated
  45120. tosylmethyl
  45121. propen
  45122. functioned
  45123. dilithio
  45124. dilution
  45125. dimboa
  45126. dimer
  45127. dimeric
  45128. dimerises
  45129. dimers
  45130. dimethanol
  45131. dimethoxyethane
  45132. dimethoxytetrahydrof
  45133. dimethyl
  45134. hylacetals
  45135. dimethylamino
  45136. dimethylbenzo
  45137. dimethylbutadiene
  45138. dimethylcyclopentano
  45139. dimethylcyclopropyl
  45140. dimethyldioxirane
  45141. dimethylformamide
  45142. dimethylhydrazone
  45143. dimethylhydrazone
  45144. dimethylimidazolidiu
  45145. dimethylindene
  45146. dimethylindole
  45147. dimethyllbenzofuran
  45148. dimethylmaleate
  45149. dimethylspiro
  45150. dimethylsulfonium
  45151. dimethylsulphonium
  45152. dinitro
  45153. dioate
  45154. gives
  45155. cyclized
  45156. material
  45157. diols
  45158. diolswere
  45159. dione
  45160. diones
  45161. dioxan
  45162. dioxane
  45163. dioxaspiro
  45164. dioxetane
  45165. dioxetanes
  45166. dioxides
  45167. dioxirane
  45168. dioxocarboxylic
  45169. dioxolan
  45170. dioxolanes
  45171. dipeptide
  45172. dipfc
  45173. diphenic
  45174. diphenyl
  45175. diphenylacetylene
  45176. diphenyldiazomethane
  45177. diphenylmethyl
  45178. diphenylphosphino
  45179. diphenylphosphinoyla
  45180. diphosphine
  45181. dipolar
  45182. dipolarophile
  45183. dipolarophiles
  45184. dipole
  45185. dipoles
  45186. direct
  45187. direct
  45188. directed
  45189. directing
  45190. directly
  45191. directs
  45192. dirhodium
  45193. disclosed
  45194. discrimination
  45195. discussed
  45196. disparlure
  45197. disparlure
  45198. containing
  45199. isolated
  45200. epoxide
  45201. functional
  45202. dispiroketal
  45203. displacement
  45204. displacements
  45205. displayed
  45206. displays
  45207. dispoke
  45208. disposed
  45209. dissociate
  45210. dissociation
  45211. dissymmetric
  45212. distal
  45213. distances
  45214. disulfonimide
  45215. diterpene
  45216. dithian
  45217. dithiane
  45218. dithianes
  45219. dithioacetals
  45220. dithioketals
  45221. dithiol
  45222. dithiolan
  45223. dithiolium
  45224. ditroc
  45225. divided
  45226. divinyl
  45227. diylbis
  45228. diyne
  45229. dmf-thf
  45230. dmso/dbu
  45231. docetaxel
  45232. dodecanones
  45233. dodecapentaenoic
  45234. dolabellane
  45235. dominates
  45236. donating
  45237. donnor
  45238. donor
  45239. double
  45240. doublebond
  45241. doubly
  45242. 7.5/1
  45243. dramatic
  45244. dramatically
  45245. dynamic
  45246. dynemicin
  45247. me3sicl
  45248. adamantone
  45249. isomer
  45250. provides
  45251. under
  45252. thermal
  45253. conditions
  45254. however
  45255. corey
  45256. clco2et
  45257. n-decane
  45258. p-clbn
  45259. phchoh
  45260. phnhcs
  45261. ph2coh
  45262. olefin
  45263. gives
  45264. corresponding
  45265. isomer
  45266. olefin
  45267. gives
  45268. corresponding
  45269. isomer
  45270. oxime
  45271. ether
  45272. shows
  45273. better
  45274. selectivity
  45275. oxime
  45276. prins
  45277. pinacol
  45278. rearrangement
  45279. selectivity
  45280. decreases
  45281. order
  45282. z/trans
  45283. e/trans
  45284. e/cis
  45285. sevier
  45286. e-boron
  45287. e/cis
  45288. e/trans
  45289. eapbh
  45290. earance
  45291. earlier
  45292. early
  45293. easily
  45294. economically
  45295. ffected
  45296. effective
  45297. effectively
  45298. effectiveness
  45299. effects
  45300. effects
  45301. efficacy
  45302. efficiency
  45303. efficient
  45304. efficient
  45305. access
  45306. tetrahydropyran
  45307. derivatives
  45308. highly
  45309. efficient
  45310. conversion
  45311. alkenes
  45312. acetals
  45313. achieved
  45314. efficiently
  45315. effort
  45316. eight
  45317. either
  45318. elaborated
  45319. elaboration
  45320. electrochemically
  45321. electrochemically
  45322. prepared
  45323. cyclohexadiene
  45324. ylide
  45325. electron
  45326. electronic
  45327. electrophilc
  45328. electrophile
  45329. electrophiles
  45330. iodine
  45331. quench
  45332. electrophilic
  45333. electrophilic
  45334. electrophilically
  45335. electrophilically
  45336. initiated
  45337. group
  45338. migration
  45339. eliminat
  45340. electrostatic
  45341. elemental
  45342. elevated
  45343. imination
  45344. ellagitannin
  45345. ellis
  45346. ellis
  45347. horwood
  45348. ellis
  45349. horwood
  45350. ellis
  45351. horwood
  45352. wiley
  45353. science
  45354. elsev
  45355. elsev
  45356. elsevier
  45357. elsevier
  45358. science
  45359. elucidate
  45360. elucidated
  45361. embodying
  45362. emerges
  45363. emmons
  45364. emphasis
  45365. employed
  45366. employing
  45367. employing
  45368. employment
  45369. enamide
  45370. enamides
  45371. enamine
  45372. enamines
  45373. enamino
  45374. enantio
  45375. enantiocontrol
  45376. enantiomer
  45377. enantiomeric
  45378. enantiomerically
  45379. enantiomers
  45380. enantiopure
  45381. enantioselection
  45382. enantioselective
  45383. enantioselective
  45384. induction
  45385. chiral
  45386. lithium
  45387. alkoxides
  45388. enantioselective
  45389. reduction
  45390. using
  45391. r-oxazaborolidine
  45392. synth
  45393. enantioselectively
  45394. enantioselectivities
  45395. enantioselectivity
  45396. enantiospecific
  45397. enarnides
  45398. endo/exo
  45399. endo/exo
  45400. selectivity
  45401. endoperoxides
  45402. enediyne
  45403. enediynes
  45404. enehydroxylamines
  45405. enehydroxylamines
  45406. react
  45407. readily
  45408. presence
  45409. energy
  45410. eneyne
  45411. eneyne
  45412. allenes
  45413. generated
  45414. sigmatropic
  45415. shiftswill
  45416. enhanced
  45417. enhanced
  45418. kinetic
  45419. acidity
  45420. coordination
  45421. enhancement
  45422. enhances
  45423. enlargement
  45424. enol/keto
  45425. enolate
  45426. enolates
  45427. enolisation
  45428. enolise
  45429. enoltriflates
  45430. enone
  45431. enones
  45432. riched
  45433. ent-4
  45434. enthalpies
  45435. entire
  45436. entropies
  45437. entry
  45438. enylphosphonates
  45439. enyne
  45440. enynes
  45441. enzyme
  45442. thieme
  45443. verlag
  45444. ephedrine
  45445. epibatidine
  45446. epibatidine
  45447. analog
  45448. epimeric
  45449. epimerization
  45450. epimerized
  45451. episulfonium
  45452. epoxidation
  45453. epoxide
  45454. epoxy
  45455. epoxyallcyl
  45456. epoxysulfoxides
  45457. equal
  45458. equation
  45459. equatorial
  45460. equilibrate
  45461. equilibrated
  45462. equilibrates
  45463. equilibration
  45464. equilibria
  45465. equimolar
  45466. equiv
  45467. equivalent
  45468. equivalents
  45469. error
  45470. erythritol
  45471. erythro/threo
  45472. erythronolide
  45473. eschenmoser
  45474. essential
  45475. essentially
  45476. establish
  45477. established
  45478. establishment
  45479. ester
  45480. esterfied
  45481. estergroups
  45482. esterification
  45483. esters
  45484. et2alcl
  45485. et2co
  45486. et2nh
  45487. et3sih
  45488. ethanoanthracenes
  45489. ethanol
  45490. ethanolamine
  45491. ethenes
  45492. etheno
  45493. ethenyl
  45494. ethenylthio
  45495. ether
  45496. etherate
  45497. ethereal
  45498. ethers
  45499. etheter
  45500. ethoxides
  45501. ethoxy
  45502. ethoxy
  45503. vinyl
  45504. ester
  45505. novel
  45506. efficient
  45507. reagent
  45508. ethoxybut
  45509. ethoxycarbonyl
  45510. ethoxyisoindol
  45511. ethoxypyrrolin
  45512. ethoxyvinyllithium
  45513. ethyl
  45514. ethyl
  45515. carboline
  45516. carboxylate
  45517. methyl
  45518. methyl
  45519. ethylated
  45520. ethylene
  45521. ethylphenylketen
  45522. ethylvinyl
  45523. ethynyl
  45524. etni-pr2
  45525. eugen
  45526. euryfuran
  45527. evaluated
  45528. evaluation
  45529. evans
  45530. evans-mislow
  45531. event
  45532. eventually
  45533. evidence
  45534. evidenced
  45535. evidense
  45536. ethoxyvinyllithium
  45537. ch2ch2
  45538. c4h9br
  45539. examined
  45540. examples
  45541. except
  45542. exceptions
  45543. excess
  45544. excesses
  45545. exchange
  45546. excision
  45547. excitatory
  45548. exclusive
  45549. exclusively
  45550. exerted
  45551. exhibit
  45552. exhibits
  45553. existence
  45554. exomethylene
  45555. expansion
  45556. expected
  45557. expectedcycloadducts
  45558. expedient
  45559. expeditious
  45560. expensive
  45561. experiment
  45562. experimental
  45563. experiments
  45564. explain
  45565. explained
  45566. explanation
  45567. exploiting
  45568. explored
  45569. extending
  45570. extends
  45571. external
  45572. extremely
  45573. extrusion
  45574. fabricated
  45575. facially
  45576. facially
  45577. dissymmetric
  45578. maleic
  45579. anhydride
  45580. synthesized
  45581. facile
  45582. facilitated
  45583. factors
  45584. facts
  45585. failed
  45586. fallis
  45587. family
  45588. fashion
  45589. faster
  45590. fatter
  45591. fatty
  45592. favor
  45593. favorable
  45594. favoring
  45595. favoured
  45596. feasibility
  45597. feasible
  45598. featured
  45599. features
  45600. features
  45601. featuring
  45602. felkin-anh
  45603. felkin/anti-felkin
  45604. ferrier
  45605. ferrocene
  45606. ferrocenes
  45607. field
  45608. filtered
  45609. finally
  45610. finding
  45611. first
  45612. ective
  45613. copper
  45614. catalyzed
  45615. insertion
  45616. yields
  45617. first
  45618. yield
  45619. flash
  45620. flask
  45621. fleming
  45622. flexible
  45623. flood
  45624. fluoride
  45625. fluorides
  45626. fluorinated
  45627. fluorination
  45628. fluorine
  45629. fluorine
  45630. facilitated
  45631. claisen
  45632. rearrangement
  45633. employed
  45634. fluoro
  45635. fluorobenzenesulfoni
  45636. fluorohydrin
  45637. fluoroketones
  45638. fluoromethyl
  45639. fluoromethylketones
  45640. fluoromethylketones
  45641. synthesized
  45642. yields
  45643. fluoropyrrole
  45644. followed
  45645. followed
  45646. following
  45647. following
  45648. homologation
  45649. sequence
  45650. readily
  45651. available
  45652. follows
  45653. follwed
  45654. review
  45655. lateral
  45656. metalation
  45657. react
  45658. allenes
  45659. involved
  45660. cobalt
  45661. mediated
  45662. force
  45663. forcing
  45664. formal
  45665. formaldehyde
  45666. formamidine
  45667. formamidines
  45668. formation
  45669. formation
  45670. membered
  45671. rings
  45672. formed
  45673. formyl
  45674. forthe
  45675. found
  45676. foundby
  45677. fourth
  45678. fragment
  45679. fragmentation
  45680. framework
  45681. radical
  45682. annulation
  45683. followed
  45684. trimethylsilyl
  45685. iodide
  45686. radical
  45687. reaction
  45688. haroalkylbicyclo
  45689. 4.2.0
  45690. freeman
  45691. fridamycin
  45692. fridamycin
  45693. derivatives
  45694. fridamycin
  45695. enantiopure
  45696. friedel
  45697. chiral
  45698. derivatives
  45699. frozen
  45700. fully
  45701. partially
  45702. mis-matched
  45703. double
  45704. stereodifferentiatin
  45705. fumarate
  45706. fumaronitrile
  45707. function
  45708. functional
  45709. functionalisation
  45710. functionalised
  45711. functionalities
  45712. functionality
  45713. functionalized
  45714. functioned
  45715. functionnalized
  45716. functions
  45717. furan
  45718. furan
  45719. nucleus
  45720. abounds
  45721. naturally
  45722. occurring
  45723. oxygen
  45724. containi
  45725. furanocembranolides
  45726. furanoid
  45727. furanone
  45728. furanones
  45729. furanopyranes
  45730. furanos
  45731. furanose
  45732. furanosesquiterpenes
  45733. furans
  45734. furfural
  45735. furnish
  45736. furnishes
  45737. furnishing
  45738. further
  45739. further
  45740. studies
  45741. addition
  45742. carbon
  45743. centred
  45744. radicalsto
  45745. furthermore
  45746. furyl
  45747. fused
  45748. fused
  45749. fused
  45750. thiadiazoles
  45751. conveniently
  45752. fused
  45753. tricyclic
  45754. compounds
  45755. salient
  45756. features
  45757. future
  45758. thieme
  45759. verlag
  45760. phenylsulfinyl
  45761. unsaturated
  45762. aldehydes
  45763. prepared
  45764. gained
  45765. gamma
  45766. gamma
  45767. heterosubstituted
  45768. vinylthionium
  45769. regioselectively
  45770. gardneria
  45771. gassman
  45772. gassman
  45773. gaveselectively
  45774. thieme
  45775. verlag
  45776. general
  45777. generally
  45778. generate
  45779. generated
  45780. generating
  45781. generation
  45782. generation
  45783. intramolecularly
  45784. tethered
  45785. nonracemic
  45786. diaryl
  45787. generation/cycloaddi
  45788. geoffrey
  45789. geoffrey
  45790. cordell
  45791. academic
  45792. press
  45793. geometries
  45794. geometry
  45795. thieme
  45796. verlag
  45797. georg
  45798. georg
  45799. georg
  45800. georg
  45801. georg
  45802. verlag
  45803. georg
  45804. theme
  45805. verlag
  45806. georg
  45807. verlag
  45808. georg
  45809. thieme
  45810. georg
  45811. thieme
  45812. georg
  45813. thieme
  45814. georg
  45815. thieme
  45816. georg
  45817. thieme
  45818. verla
  45819. georg
  45820. thieme
  45821. verlag
  45822. georg
  45823. thieme
  45824. verlag
  45825. georg
  45826. thieme
  45827. verlag
  45828. george
  45829. george
  45830. thieme
  45831. verlag
  45832. gerald
  45833. gerald
  45834. larson
  45835. press
  45836. greenwich
  45837. germanium
  45838. given
  45839. gives
  45840. giving
  45841. glucal
  45842. glucose
  45843. glucosidase
  45844. glutamate
  45845. glutamic
  45846. glutarimide
  45847. glyceraldehyde
  45848. glycidic
  45849. glycidol
  45850. glycidyl
  45851. glycine
  45852. glycol
  45853. glycoprotein
  45854. glycosides
  45855. glyoxal
  45856. glyoxylate
  45857. glyoxylic
  45858. gordon
  45859. breach
  45860. governed
  45861. greater
  45862. greatly
  45863. greatly
  45864. greenwich
  45865. grierson
  45866. grigg
  45867. grignard
  45868. ground
  45869. group
  45870. gruyter
  45871. guaianolides
  45872. studies
  45873. dihydroquinidinyl
  45874. terephthalate
  45875. yamamoto
  45876. tetrahedron
  45877. h2so4
  45878. h3-h1
  45879. haack
  45880. halide
  45881. halides
  45882. haloaldimines
  45883. haloamides
  45884. haloesters
  45885. halogen
  45886. halogenoacyl
  45887. halogenoacylindoles
  45888. haloketenes
  45889. halolactonization
  45890. handle
  45891. hantzsch
  45892. harnesses
  45893. haroalkylbicyclo
  45894. harwood
  45895. harwood
  45896. academic
  45897. having
  45898. having
  45899. r2net
  45900. h2so4
  45901. khso4
  45902. effective
  45903. place
  45904. hcl/ether
  45905. heathcock
  45906. heating
  45907. heating
  45908. diastereomeric
  45909. chiral
  45910. biaryls
  45911. helvetica
  45912. hemiacetals
  45913. hemiaminal
  45914. hemishere
  45915. heptadienes
  45916. heptane
  45917. heptapeptides
  45918. heptenoic
  45919. heptonolactones
  45920. heptyn
  45921. herein
  45922. hetaryl
  45923. hetero
  45924. hetero
  45925. diels
  45926. alder
  45927. reaction
  45928. oxadienes
  45929. epoxy
  45930. heteroaromatic
  45931. heteroaryl
  45932. heteroatom
  45933. heteroatoms
  45934. heterocycle
  45935. heterocycles
  45936. heterocyclic
  45937. heterodimers
  45938. heterogeneous
  45939. heterosubstituted
  45940. heterotricyclic
  45941. hexaamine
  45942. hexadecan
  45943. hexafluorophosphate
  45944. hexahydro
  45945. hexamethyldisilamide
  45946. hexamethyldisilazane
  45947. hexan
  45948. hexane
  45949. hexen
  45950. hexene
  45951. hexenylamines
  45952. hexenyllithiums
  45953. hexonolactones
  45954. hexynes
  45955. barrier
  45956. rotation
  45957. diastereoselectivity
  45958. conjugate
  45959. addition
  45960. lithi
  45961. pressure
  45962. substantially
  45963. increases
  45964. lifetime
  45965. yield
  45966. halides
  45967. mediated
  45968. reactions
  45969. between
  45970. thioacid
  45971. higher
  45972. highly
  45973. himachalene
  45974. himalayan
  45975. hindered
  45976. hindrance
  45977. histrionicotoxin
  45978. hoch2so2na
  45979. hodhbt
  45980. homachiral
  45981. homallylic
  45982. homoallylic
  45983. homochiral
  45984. homochiralcyclopenta
  45985. homogeranic
  45986. homolog
  45987. homologated
  45988. homologation
  45989. homolysis
  45990. homolytic
  45991. homopropargylic
  45992. horner
  45993. hosomi
  45994. however
  45995. hstips
  45996. hunig's
  45997. hydoxyl
  45998. hydration
  45999. hydrazines
  46000. hydrazoic
  46001. hydrazone
  46002. hydrazones
  46003. hydride
  46004. hydride
  46005. hydrides
  46006. hydroborating
  46007. hydroboration
  46008. hydroboration-coupli
  46009. oride
  46010. hydrocinnamaldehyde
  46011. hydrocyanation
  46012. hydrocyanation
  46013. cyclic
  46014. alpha
  46015. sulfinyl
  46016. ketones
  46017. under
  46018. differ
  46019. hydroformylation
  46020. hydrogen
  46021. hydrogenation
  46022. hydrogenolysis
  46023. hydrogens
  46024. hydrogensulfate
  46025. hydrohalogenation
  46026. hydroisoquinoline
  46027. hydrolysis
  46028. hydrolytic
  46029. hydrolyzed
  46030. hydroperoxide
  46031. hydrosilylations
  46032. hydrosilylations
  46033. styrene
  46034. cyclopentadiene
  46035. performe
  46036. hydrostannylation
  46037. hydrotribromide
  46038. hydroxamic
  46039. hydroxide
  46040. hydroximoyl
  46041. hydroximoyl
  46042. chlorides
  46043. bearing
  46044. alpha
  46045. chloro
  46046. functionality
  46047. hydroxy
  46048. hydroxy
  46049. hydroxyacids
  46050. hydroxyaldehyde
  46051. hydroxycyanohydrin
  46052. hydroxycyanohydrins
  46053. hydroxycyclohexanone
  46054. hydroxyethylene
  46055. hydroxyindolizidine
  46056. hydroxyisocoumarin
  46057. hydroxyketones
  46058. hydroxyl
  46059. hydroxylactams
  46060. hydroxylamine
  46061. hydroxylamines
  46062. hydroxylation
  46063. hydroxylysine
  46064. hydroxymethyl
  46065. hydroxymethylcyclopr
  46066. hydroxyoctahydroisoc
  46067. hydroxyphenylsulfone
  46068. hydroxypiperidines
  46069. hydroxypyridine
  46070. hydroxystannanes
  46071. hydrozirconation
  46072. hypervalent
  46073. hypervalent
  46074. iodine
  46075. oxidation
  46076. methyl
  46077. quinolones
  46078. using
  46079. icand
  46080. identified
  46081. identify
  46082. illustrate
  46083. illustrated
  46084. image
  46085. imidate
  46086. imidates
  46087. imidates
  46088. thioimidates
  46089. bearing
  46090. butylstanny
  46091. imidazolidinone
  46092. imide
  46093. imides
  46094. imine
  46095. imines
  46096. imino
  46097. iminophosphoranes
  46098. immediate
  46099. implicate
  46100. implies
  46101. important
  46102. impossible
  46103. impressive
  46104. improved
  46105. improvement
  46106. improving
  46107. eactio
  46108. general
  46109. yields
  46110. dipolar
  46111. cycloaddition
  46112. cyclic
  46113. nitrone
  46114. icand
  46115. presence
  46116. catalytic
  46117. amount
  46118. scandium
  46119. perchl
  46120. presence
  46121. equimolar
  46122. amounts
  46123. alkoxide
  46124. inactivates
  46125. incipient
  46126. include
  46127. includes
  46128. includes11
  46129. including
  46130. incorporated
  46131. incorporating
  46132. incorporation
  46133. increase
  46134. increased
  46135. increases
  46136. increasing
  46137. indicate
  46138. indicated
  46139. indicates
  46140. indol
  46141. indole
  46142. indoles
  46143. indolizidine
  46144. indolizinone
  46145. indolyldihydrodyridi
  46146. indolylmethyl
  46147. induce
  46148. induced
  46149. induction
  46150. inefficient
  46151. influence
  46152. indacene@
  46153. influence
  46154. inter
  46155. intramolecular
  46156. trapping
  46157. radical
  46158. species@
  46159. intermediate
  46160. intramolecular
  46161. cycloaddition
  46162. diaryl
  46163. heptadiene@
  46164. intramolecular
  46165. diazoketoester
  46166. thiolmide
  46167. annulation
  46168. reaction
  46169. iodides@
  46170. iodine
  46171. ionic@
  46172. isopropyl@
  46173. mannostatin@
  46174. mechanism
  46175. metal
  46176. methyl
  46177. methylnaphthalene@
  46178. mixture
  46179. catalyzes
  46180. cross
  46181. coupli@
  46182. monosubstituted
  46183. alkoxycarbonyl
  46184. arylsulfonyl
  46185. lactams
  46186. prepar@
  46187. naturally
  46188. nickel
  46189. complexes
  46190. having
  46191. diketone-type
  46192. ligands
  46193. number
  46194. ofchiral@
  46195. optical@
  46196. order
  46197. other
  46198. oxanorbornadieno@
  46199. oxidation
  46200. product
  46201. shown
  46202. sodium
  46203. metaperiodate
  46204. affords@
  46205. influence
  46206. influences
  46207. information
  46208. inhibit
  46209. inhibition
  46210. inhibitor
  46211. inhibitors
  46212. inhibitors
  46213. concentration
  46214. inhibit
  46215. reaction
  46216. inhibitory
  46217. initial
  46218. initially
  46219. initiate
  46220. initiated
  46221. initiation
  46222. initio
  46223. initital
  46224. inmoderate
  46225. insertion
  46226. inserts
  46227. insight
  46228. installing
  46229. instance
  46230. instances
  46231. instantaneous
  46232. instead
  46233. intact
  46234. inter
  46235. radical
  46236. species
  46237. interaction
  46238. intercalative
  46239. intercepted
  46240. interchange
  46241. interesting
  46242. intermediacy
  46243. intermediary
  46244. intermediate
  46245. intermediate
  46246. intermediates
  46247. intermolecular
  46248. internal
  46249. interpretation
  46250. interpreted
  46251. intervention
  46252. inthe
  46253. intramolecular
  46254. ptadiene
  46255. intramolecular
  46256. capture
  46257. pyrroles
  46258. vinyl
  46259. carbenoids
  46260. gener
  46261. intramolecular
  46262. coupling
  46263. using
  46264. stereocontrolling
  46265. linking
  46266. intramolecular
  46267. cyclization
  46268. benzylic
  46269. cations
  46270. derived
  46271. intramolecular
  46272. diazoketoester
  46273. thiolmide
  46274. annulation
  46275. reaction
  46276. intramolecular
  46277. alkylation
  46278. glucose
  46279. derived
  46280. substrate
  46281. intramolecular
  46282. nucleophile
  46283. transfer
  46284. reaction
  46285. several
  46286. intramolecular
  46287. pauson
  46288. khand
  46289. reactions
  46290. enynes
  46291. intramolecular
  46292. photocycloaddition
  46293. pyridones
  46294. joined
  46295. intramolecular
  46296. tishchenko
  46297. reaction
  46298. intramolecular
  46299. ureidomercuration
  46300. aminoacids
  46301. synthesi
  46302. intramolecularly
  46303. intriguingly
  46304. intrinsic
  46305. introduce
  46306. introduced
  46307. introduction
  46308. inversion
  46309. inverted
  46310. investigated
  46311. investigations
  46312. involve
  46313. involved
  46314. involves
  46315. involvesa
  46316. involving
  46317. iodide
  46318. iodinated
  46319. iodine
  46320. iodine
  46321. iodine
  46322. promoted
  46323. decomposition
  46324. dialkyltriazenes
  46325. iodine/hydrogen
  46326. iodoacrylic
  46327. iodoalkanes
  46328. iodoalkyl
  46329. iodoanilide
  46330. iodobicyclo
  46331. iodocyclohexyl
  46332. iododienone
  46333. iodoesters
  46334. iodolactonization
  46335. iodomethylzinc
  46336. iodonium
  46337. iodonorcarane
  46338. iodophenyl
  46339. iodos
  46340. iodotrienone
  46341. iodotrimethylsilane
  46342. mechanism
  46343. ionization
  46344. ipcbh
  46345. ipr2net
  46346. ipsenol
  46347. iridoid
  46348. press
  46349. irradiated
  46350. irradiation
  46351. irradiation
  46352. acetylenic
  46353. ethers
  46354. methanol
  46355. gives
  46356. homologat
  46357. irradiation
  46358. taxol
  46359. rayonet
  46360. reactor
  46361. yielded
  46362. irrespective
  46363. irreversible
  46364. isable
  46365. ishii
  46366. isoamyl
  46367. isobellendine
  46368. isoborneol
  46369. isobutylene
  46370. isobutyraldehyde
  46371. isocyanate
  46372. isocyanates
  46373. isocyanicacid
  46374. isocyano
  46375. isodiazomethane
  46376. isokinetic
  46377. isolable
  46378. isolated
  46379. isolation
  46380. isolobophytolide
  46381. isomer
  46382. isomeric
  46383. isomerically
  46384. isomerise
  46385. isomerization
  46386. isomerize
  46387. isomers
  46388. isophorone
  46389. isopinocampheylboran
  46390. isoprene
  46391. isopropanol
  46392. isopropoxy
  46393. soseiridine
  46394. isostere
  46395. isosteres
  46396. isoxazoles
  46397. isoxazoline
  46398. isoxazolines
  46399. issue
  46400. itself
  46401. itsuno's
  46402. 1986108
  46403. press
  46404. press
  46405. james
  46406. james
  46407. coxon
  46408. press
  46409. greenwich
  46410. january
  46411. january
  46412. japan
  46413. press
  46414. jeffrey
  46415. jeffrey
  46416. seeman
  46417. wiley
  46418. wiley
  46419. wiley
  46420. wiley
  46421. johnson
  46422. joined
  46423. jorgensen
  46424. ketenes
  46425. ketenimines
  46426. ketimine
  46427. ketoaldehyde
  46428. ketoester
  46429. ketoester
  46430. ketoesters
  46431. ketohydrazones
  46432. ketoimines
  46433. ketone
  46434. shown
  46435. direct
  46436. epoxidation
  46437. ketones
  46438. ketonization
  46439. intermediate
  46440. synthesis
  46441. erythronolide
  46442. syntheses
  46443. shown
  46444. below
  46445. target
  46446. cephalotaxinel
  46447. total
  46448. synthesis
  46449. synthesis
  46450. lacrimin
  46451. first
  46452. enantioselective
  46453. synthesis
  46454. cortison
  46455. total
  46456. synthesis
  46457. tazettine
  46458. 6a-epipreta
  46459. thienamycin
  46460. synthesis
  46461. total
  46462. synthesis
  46463. isolobophytolide
  46464. crassin
  46465. total
  46466. synthesis
  46467. isolobophytolide
  46468. crassin
  46469. towards
  46470. synthesis
  46471. yohimbine
  46472. towards
  46473. syntheses
  46474. histrionicotoxin
  46475. keyintermediate
  46476. kf/hcl
  46477. khand
  46478. kharasch
  46479. khmds
  46480. khso4
  46481. kiado
  46482. kibayashi
  46483. killers
  46484. kinectic
  46485. kinetic
  46486. enolates
  46487. number
  46488. alpha
  46489. dibenzyl
  46490. aminometh
  46491. kinetics
  46492. kluwe
  46493. kluwer
  46494. kluwer
  46495. academic
  46496. known
  46497. kococf3
  46498. kodansha
  46499. kodansha
  46500. koh-diamine
  46501. kstips
  46502. glutamic
  46503. diethyl
  46504. ester
  46505. hydrochloride
  46506. converted
  46507. labeled
  46508. labeling
  46509. labelling
  46510. lacking
  46511. lacks
  46512. lacrimin
  46513. lactam
  46514. lactams
  46515. lactone
  46516. lactones
  46517. lahotbu3
  46518. lanier
  46519. lanny
  46520. lanny
  46521. liebeskind
  46522. press
  46523. greenwich
  46524. lanthanide
  46525. larger
  46526. largest
  46527. larson
  46528. latter
  46529. 44'-di-tert-butylbip
  46530. leading
  46531. leading
  46532. references
  46533. leads
  46534. leads
  46535. leaving
  46536. reactive
  46537. nitroanilines
  46538. unsuccesfully
  46539. reacted
  46540. leusen
  46541. level
  46542. levels
  46543. lewis
  46544. lewis
  46545. catalyzed
  46546. cyclization
  46547. lactones
  46548. orcyclohexa
  46549. enolates
  46550. readily
  46551. converted
  46552. enolates
  46553. treatmen
  46554. lialh4
  46555. liberated
  46556. licable
  46557. lication
  46558. deactivates
  46559. reaction
  46560. product
  46561. formed
  46562. synthesi
  46563. liclic
  46564. liclo4
  46565. liebeskind
  46566. lifetime
  46567. ligand
  46568. ligandsreact
  46569. light
  46570. liica
  46571. liica
  46572. lithium
  46573. n-cyclohexyl-n-isopr
  46574. likely
  46575. limit
  46576. limitation
  46577. limitations
  46578. limited
  46579. limited
  46580. benzyl
  46581. cinnamyl
  46582. alcohols
  46583. limonene
  46584. linear
  46585. linkage
  46586. linking
  46587. lipoxygenase
  46588. literature
  46589. lithiated
  46590. lithiation
  46591. lithio
  46592. lithiobutylindenide
  46593. lithiodithiane
  46594. lithiodithianes
  46595. lithioheterocycles
  46596. lithiomethylene
  46597. lithiooxazolidines
  46598. lithiothiophene
  46599. lithium
  46600. lower
  46601. lowerbut
  46602. lowered
  46603. luche
  46604. ly280810
  46605. dekker
  46606. macrocycles
  46607. macrocyclisation
  46608. macrocyclization
  46609. macrolactamization
  46610. magnesium
  46611. magnesium
  46612. salts
  46613. reaction
  46614. magnetic
  46615. mainly
  46616. major
  46617. major
  46618. diastereomer
  46619. configuration
  46620. majority
  46621. makes
  46622. making
  46623. maleate
  46624. maleic
  46625. maleimide
  46626. malonate
  46627. malonates
  46628. malonic
  46629. malonic
  46630. esters
  46631. ester
  46632. other
  46633. methylene
  46634. active
  46635. compo
  46636. mandelate
  46637. manganese
  46638. manipulations
  46639. manner
  46640. mannich
  46641. mannostatin
  46642. examples
  46643. 30-95
  46644. regioselectivity
  46645. examples
  46646. 76-93
  46647. examples
  46648. stereoselective
  46649. carbocyclization
  46650. further
  46651. examples
  46652. further
  46653. examples
  46654. 70-97
  46655. yields
  46656. manzamine
  46657. marcel
  46658. marcel
  46659. dekker
  46660. marine
  46661. marked
  46662. markedly
  46663. markovnikov
  46664. martin
  46665. masamune
  46666. matched
  46667. material
  46668. materials
  46669. mayoccur
  46670. mccombie
  46671. mcgraw
  46672. mcgraw
  46673. mckelvie
  46674. mcmurry
  46675. mcpba
  46676. mcscf/3
  46677. me2cu
  46678. me3sicl
  46679. me3sisna
  46680. me3sncl
  46681. means
  46682. measure
  46683. measured
  46684. measurements
  46685. mechanics
  46686. mechanism
  46687. mechanism
  46688. mechanisms
  46689. mechanistic
  46690. mechanistically
  46691. mechanistically
  46692. reaction
  46693. proceeds
  46694. pericyc
  46695. media
  46696. mediate
  46697. mediated
  46698. mediates
  46699. medical
  46700. medium
  46701. member
  46702. membered
  46703. memgi
  46704. meno2
  46705. ercaptane
  46706. mercapto
  46707. mercaptoethyl
  46708. mercuric
  46709. merhane
  46710. merlic
  46711. meser
  46712. mesitaldehyde
  46713. mesityl
  46714. mesitylthio
  46715. mesyl
  46716. mesylates
  46717. mesylcyanohydrins
  46718. metal
  46719. metal
  46720. metalation
  46721. metallated
  46722. metalloenamines
  46723. metals
  46724. metaperiodate
  46725. metathesis
  46726. methacrylate
  46727. methacryloylsultam
  46728. methallylsilanes
  46729. methane
  46730. methanesulfenyl
  46731. methanoanthracene
  46732. methanol
  46733. methanolic
  46734. methanolysis
  46735. methides
  46736. methine
  46737. methl
  46738. method
  46739. methodologies
  46740. methodology
  46741. methods
  46742. methods
  46743. preparation
  46744. trimethylsilyl
  46745. thioph
  46746. methoxy
  46747. methoxyacetic
  46748. methoxybenzamides
  46749. methoxycarbonyl
  46750. methoxycarbonylbenzo
  46751. methoxycarbonylethyn
  46752. methoxyfuran
  46753. methoxymethyl
  46754. methoxyphenethylamin
  46755. methoxyphenol
  46756. methyl
  46757. methyl
  46758. methylacetoacetate
  46759. methylalkylamines
  46760. methylalumination
  46761. methylamine
  46762. methylation
  46763. methylbenzimidazolon
  46764. methylbenzothiazoles
  46765. methylbenzylamine
  46766. methylbenzyloxy
  46767. methylcarbapenem
  46768. methylcarbapenems
  46769. methylcarbonate
  46770. methylcarbonates
  46771. methylcarboximidoyl
  46772. methylchloride
  46773. methylenation
  46774. methylene
  46775. methylenebicyclo
  46776. methylenecyclobutane
  46777. methylenecyclopropyl
  46778. methylenedioxy
  46779. methylenetricyclo
  46780. methylester
  46781. methylethenyltrimeth
  46782. methylhydroxylamine
  46783. methylide
  46784. methyllithium
  46785. methylmaleimide
  46786. methylmeldrum's
  46787. methylnaphthalene
  46788. methylphenyl
  46789. methylpiperidine
  46790. methylpropane
  46791. methylpyrrolidine
  46792. methylserine
  46793. methylstannanes
  46794. methylstyrene
  46795. methyltetracyclo
  46796. methylthiazole
  46797. methylthio
  46798. methyltricyclo
  46799. methyltrimethylsilan
  46800. meyer
  46801. meyers
  46802. mgbr-cecl3
  46803. mgbr2
  46804. mgbrx
  46805. michael
  46806. microwave
  46807. migrating
  46808. migration
  46809. milbemycins
  46810. mildness
  46811. millipede
  46812. mimicking
  46813. mimickingthe
  46814. minimized
  46815. minor
  46816. mirror
  46817. mis-matched
  46818. mistry
  46819. mitsunobu
  46820. mixing
  46821. mixture
  46822. mixture
  46823. products
  46824. mixture
  46825. catalyzes
  46826. cross
  46827. coupli
  46828. mixtures
  46829. model
  46830. modelcompounds
  46831. moderate
  46832. moderately
  46833. modes
  46834. modest
  46835. modification
  46836. modifications
  46837. modified
  46838. modifiers
  46839. moieties
  46840. moiety
  46841. moisture
  46842. molecule
  46843. molecules
  46844. molybdenum
  46845. monitored
  46846. addition
  46847. lactones
  46848. facilitated
  46849. cecl3
  46850. monoactivated
  46851. monoalkylated
  46852. monocarbonyl
  46853. monocoupling
  46854. monoesters
  46855. monohemiketal
  46856. monolithium
  46857. monomers
  46858. monophosphine
  46859. monosilyl
  46860. monosubstituted
  46861. monosubstituted
  46862. monosustituted
  46863. monoxide
  46864. montmorillonite
  46865. energy
  46866. partition
  46867. scheme
  46868. calculat
  46869. movement
  46870. mp4sdtq/6
  46871. muchfaster
  46872. mukaiyama
  46873. muller
  46874. mutual
  46875. mycaroside
  46876. myriocin
  46877. tokyo
  46878. japan
  46879. alkoxycarbonyl
  46880. arylsulfonyl
  46881. lactams
  46882. prepar
  46883. alkyl
  46884. cinnamyl
  46885. carbamates
  46886. prepared
  46887. yields
  46888. protected
  46889. lactams
  46890. reduced
  46891. chemoselectively
  46892. butoxycarbonyl
  46893. hydroxylamine
  46894. triflyloxy
  46895. amides
  46896. undergo
  46897. ionization
  46898. refluxing
  46899. isopropa
  46900. n-butyl
  46901. n-butylamine
  46902. n-cyclohexyl-n-isopr
  46903. n-decane
  46904. n-diethylaminotribut
  46905. n-methyl
  46906. n-oxoammonium
  46907. n-propyl
  46908. n1/n3
  46909. nabh4
  46910. nabh4
  46911. ratio
  46912. nabph4
  46913. nabph4
  46914. naoac
  46915. naoac
  46916. naphthalene
  46917. naphthalenide
  46918. naphthazarin
  46919. naphthol
  46920. naphthoquinone
  46921. naphthyl
  46922. naphthylamide
  46923. naphthyridine
  46924. naphtyridine
  46925. napieralski
  46926. napth
  46927. nateh
  46928. natural
  46929. naturally
  46930. naturally
  46931. naturally
  46932. occurring
  46933. hemiacetals
  46934. diboa
  46935. dimboa
  46936. synthe
  46937. nature
  46938. nbs/peroxide
  46939. neared
  46940. nearly
  46941. negative
  46942. negatively
  46943. neighboring
  46944. nephrosteranic
  46945. neutral
  46946. neutralize
  46947. never
  46948. nevertheless
  46949. radical
  46950. syntheses
  46951. developed
  46952. under
  46953. bartan
  46954. opening
  46955. reaction
  46956. thiiranes
  46957. carboxylic
  46958. syntheses
  46959. thiosubstituted
  46960. carbonyl
  46961. compounds
  46962. newbond
  46963. newly
  46964. nfobs
  46965. nicholas
  46966. nickel
  46967. nickel
  46968. complexes
  46969. having
  46970. diketone-type
  46971. ligands
  46972. nicolaou
  46973. nikkomycin
  46974. nitrate
  46975. nitrates
  46976. nitrile
  46977. nitriles
  46978. nitrilimines
  46979. nitrite
  46980. nitro
  46981. nitro
  46982. chloro
  46983. bromo
  46984. acetanilides
  46985. reaction
  46986. nitroalkanols
  46987. nitroallylic
  46988. nitroanilines
  46989. nitrobenzene
  46990. nitrobicyclo
  46991. nitrocycloalkanones
  46992. nitrocycloalkenes
  46993. nitrogen
  46994. nitromethane
  46995. nitrone
  46996. nitrones
  46997. nitronic
  46998. nitropolyzonamine
  46999. experiments
  47000. unequivocally
  47001. product
  47002. obtai
  47003. study
  47004. indicates
  47005. formation
  47006. higher
  47007. order
  47008. cuprate
  47009. non-chelation
  47010. nonane
  47011. nonanederivatives
  47012. nonanes
  47013. nonchelation
  47014. noncyclopropyl
  47015. nonracemic
  47016. nonultrasound
  47017. nopinone
  47018. normal
  47019. normethyl
  47020. nostrand
  47021. noted
  47022. noteworthy
  47023. notthe
  47024. novel
  47025. noveltricyclo
  47026. effect
  47027. chirality
  47028. noyori
  47029. meno2
  47030. phthalimide
  47031. tms-cn
  47032. tms-n3
  47033. methyl
  47034. acetate
  47035. dimet
  47036. nucleophile
  47037. nucleophiles
  47038. nucleophilic
  47039. withd
  47040. nucleosides
  47041. nucleus
  47042. number
  47043. number
  47044. numbers
  47045. nvestigated
  47046. nysted
  47047. nysted
  47048. conditions
  47049. ch2znbr
  47050. ticl4
  47051. benzoyl
  47052. hydroxamic
  47053. acids
  47054. react
  47055. tributylstannane
  47056. o-alkylation
  47057. observation
  47058. observed
  47059. occur
  47060. occurred
  47061. occurring
  47062. occurs
  47063. octacarbonyl
  47064. octadienes
  47065. octahydroisocoumarin
  47066. octane
  47067. octanol
  47068. octyl
  47069. ocyclic
  47070. olefination
  47071. olefinic
  47072. olefins
  47073. oligopetide
  47074. oliogosaccharide
  47075. omega
  47076. carbon
  47077. homologation
  47078. benzylic
  47079. allylic
  47080. propargylic
  47081. other
  47082. example
  47083. other
  47084. example
  47085. yield
  47086. formation
  47087. using
  47088. nucleophile
  47089. onein
  47090. ongoing
  47091. onium
  47092. diastereomer
  47093. cyclizes
  47094. metathesis
  47095. react
  47096. opening
  47097. opening
  47098. furan
  47099. concomitant
  47100. closure
  47101. cyclo
  47102. operation
  47103. opiate
  47104. opium
  47105. oppolzer's
  47106. opportunity
  47107. opposite
  47108. optical
  47109. optically
  47110. optically
  47111. active
  47112. allylic
  47113. sulphides
  47114. bearing
  47115. differe
  47116. optically
  47117. active
  47118. linear
  47119. branched
  47120. chain
  47121. phenylthio
  47122. optimization
  47123. optimization
  47124. ligand/base
  47125. solvent
  47126. provide
  47127. substitut
  47128. optimized
  47129. oracetaldehyde
  47130. orbital
  47131. orcyclohexanone
  47132. order
  47133. order
  47134. order
  47135. insertion
  47136. allyl/benzyl
  47137. methylene
  47138. methine
  47139. methyl
  47140. organoaluminum
  47141. organocopper
  47142. organolithiums
  47143. organometal
  47144. organometallic
  47145. organometallicsto
  47146. organopalladium
  47147. organoselenium
  47148. organostannanes
  47149. organsulfur
  47150. organyl
  47151. orientation
  47152. origin
  47153. original
  47154. originally
  47155. ortho
  47156. orthoacetate
  47157. orthoester
  47158. orthoesters
  47159. orthosubstituents
  47160. osmium
  47161. ot-bu
  47162. other
  47163. other
  47164. cuprate
  47165. reagents
  47166. either
  47167. addition
  47168. product
  47169. other
  47170. examples
  47171. 51-79
  47172. yield
  47173. 89-98
  47174. other
  47175. references
  47176. masamune
  47177. masamune
  47178. other
  47179. references
  47180. denmark
  47181. salle
  47182. verla
  47183. salle
  47184. verlag
  47185. outcome
  47186. outer
  47187. overall
  47188. overall
  47189. yields
  47190. range
  47191. overlap
  47192. overman
  47193. oxabicyclo
  47194. oxadienes
  47195. oxalyl
  47196. oxanorbornadieno
  47197. oxanorborneno
  47198. oxaphosphinane
  47199. oxathiolanes
  47200. oxazaborolidine
  47201. oxazaborolidines
  47202. oxazin
  47203. oxazines
  47204. oxazole
  47205. oxazoles
  47206. oxazolidin
  47207. oxazolidine
  47208. oxazolidines
  47209. oxazolidinone
  47210. oxazoline
  47211. oxazolines
  47212. oxazolines
  47213. readily
  47214. oxidized
  47215. oxazoles
  47216. using
  47217. nbs/per
  47218. oxazolopiperidine
  47219. oxazolopiperidones
  47220. oxepane
  47221. oxepinones
  47222. oxetane
  47223. oxetanes
  47224. oxford
  47225. oxford
  47226. university
  47227. press
  47228. oxidant
  47229. oxidation
  47230. oxidation
  47231. dithiolan
  47232. equivalent
  47233. oxidation
  47234. allylic
  47235. methylene
  47236. groups
  47237. under
  47238. oxidation
  47239. chiral
  47240. trimethylsilyloxy
  47241. ethers
  47242. oxidation
  47243. product
  47244. shown
  47245. sodium
  47246. metaperiodate
  47247. affords
  47248. oxidation
  47249. substituted
  47250. thietanes
  47251. chlorop
  47252. oxidations
  47253. oxidative
  47254. oxidatively
  47255. oxide
  47256. oxides
  47257. oxidized
  47258. oxidizes
  47259. oxidizing
  47260. oxime
  47261. oxime
  47262. ethers
  47263. connected
  47264. tether
  47265. aldehydes
  47266. ketones
  47267. oximes
  47268. oxindole
  47269. oxine
  47270. oxirane
  47271. oxiranes
  47272. oxoalkanedioic
  47273. oxocane
  47274. oxolanes
  47275. oxolysine
  47276. oxone
  47277. oxone
  47278. 2khso3
  47279. khso4
  47280. k2so4
  47281. oxonia
  47282. oxopipecolic
  47283. oxosecodine
  47284. oxovincadifformine
  47285. oxycarbenium
  47286. oxychloride
  47287. oxygen
  47288. oxygenation
  47289. oxygenation
  47290. works
  47291. silyl
  47292. ketene
  47293. acetals
  47294. silyl
  47295. oxygens
  47296. ozone
  47297. rgamon
  47298. p-allyl
  47299. p-anisidine
  47300. p-anisidine
  47301. protecting
  47302. group
  47303. removed
  47304. oxidatively
  47305. p-clbn
  47306. p-nitrobenzenesulfon
  47307. p-nitrobenzylesters
  47308. pairs
  47309. palladium
  47310. palladium
  47311. found
  47312. catalyse
  47313. reaction
  47314. palladium
  47315. catalyzed
  47316. cyclization
  47317. hydroisoquinoline
  47318. diene
  47319. palladium
  47320. catalyzed
  47321. oxidation
  47322. conjugated
  47323. dienes
  47324. palladium
  47325. mediated
  47326. cyclization
  47327. occurs
  47328. provide
  47329. products
  47330. pantolactone
  47331. papbh
  47332. paper
  47333. epimerization
  47334. secondary
  47335. hydroxyl
  47336. group
  47337. partial
  47338. partially
  47339. participate
  47340. participating
  47341. participation
  47342. particular
  47343. particularly
  47344. partition
  47345. partner
  47346. passing
  47347. pathway
  47348. pathwayand
  47349. pauson
  47350. pinacolborane
  47351. catalysed
  47352. cross
  47353. coupling
  47354. butenolide
  47355. triflates
  47356. pd/c/na2so4
  47357. pd/m2co3/qx
  47358. dibenzylideneacetony
  47359. bispalladium
  47360. n-met
  47361. penem
  47362. penta
  47363. pentacycle
  47364. pentacyclic
  47365. pentadecapentaenoic
  47366. pentadiene
  47367. pentane
  47368. pentannulation
  47369. penten
  47370. pentenamid
  47371. pentenylazides
  47372. peptides
  47373. peracid
  47374. perchlorate
  47375. perfluoroalkyl
  47376. performance
  47377. epimerization
  47378. secondary
  47379. hydroxyl
  47380. group@
  47381. generated
  47382. combination
  47383. tioac
  47384. promotes
  47385. performance
  47386. pergamon
  47387. pergamon
  47388. press
  47389. phenol
  47390. rapidly
  47391. reduced
  47392. samarium
  47393. diiodide
  47394. syste@
  47395. phnhcs@
  47396. phosphonobutanoic
  47397. piperidein@
  47398. plenum
  47399. york@
  47400. porphyrin@
  47401. pres@
  47402. presence
  47403. present@
  47404. press
  47405. prins@
  47406. proceed
  47407. production@
  47408. products
  47409. products
  47410. easily
  47411. converted
  47412. a-hydroxy
  47413. amides
  47414. reduc@
  47415. protected
  47416. providing@
  47417. organic
  47418. chemistry
  47419. reducing@
  47420. regio
  47421. reported
  47422. review
  47423. royal
  47424. society
  47425. chemistry
  47426. science
  47427. seems@
  47428. serine
  47429. shown
  47430. sodium
  47431. spiroketals@
  47432. starting
  47433. stereoelectronic@
  47434. stirring@
  47435. substituent
  47436. suggestion@
  47437. performance
  47438. performed
  47439. performing
  47440. press
  47441. perga
  47442. perga
  47443. press
  47444. pergam
  47445. pergam
  47446. press
  47447. pergamo
  47448. pergamo
  47449. press
  47450. pergamon
  47451. pergamon
  47452. pergamon
  47453. pergamon
  47454. pergamon
  47455. pergamon
  47456. press
  47457. pergamon
  47458. press
  47459. pergamon
  47460. press
  47461. pergamon
  47462. press
  47463. oxford
  47464. pergamon
  47465. perhydrophenanthrene
  47466. pericyclic
  47467. periodate
  47468. periplanone
  47469. permit
  47470. permitted
  47471. peroxidation
  47472. peroxide
  47473. perturbation
  47474. peterson
  47475. petrarch
  47476. petrarch
  47477. systems
  47478. ph2coh
  47479. ph3as
  47480. ph3sb
  47481. ph3snh
  47482. phase
  47483. phch2ch2
  47484. phcho
  47485. phchoh
  47486. phcoome
  47487. phenacylides
  47488. phenanthrene
  47489. phenanthridinium
  47490. phenol
  47491. phenol
  47492. rapidly
  47493. reduced
  47494. samarium
  47495. diiodide
  47496. syste
  47497. phenols
  47498. phenomenon
  47499. phenoselenyl
  47500. phenoxide
  47501. phenoxyquinolines
  47502. phenyl
  47503. phenyl1
  47504. phenylacetic
  47505. phenylacetonitrile
  47506. phenylalanine
  47507. phenylalaninol
  47508. phenyldiazoacetates
  47509. phenylglyoxal
  47510. phenylimidates
  47511. phenyliodine
  47512. phenyliodonio
  47513. phenylnitrone
  47514. phenylpentacyclo
  47515. phenylphthalic
  47516. phenylselenides
  47517. phenylseleno
  47518. phenylselenomethyl
  47519. phenylselenone
  47520. phenylsulfinyl
  47521. phenylsulfones
  47522. phenylsulfoxide
  47523. phenylthio
  47524. phenylthioazetidinon
  47525. pheomelanin
  47526. pheromone
  47527. phetane
  47528. phosphine
  47529. phosphines
  47530. phosphinoenzoyl
  47531. phospholanes
  47532. phosphonate
  47533. phosphonium
  47534. phosphoniumsalts
  47535. phosphonobutanoic
  47536. phosphonobutanoic
  47537. phosphoric
  47538. phosphorus
  47539. photo
  47540. photoaddition
  47541. photoadducts
  47542. photochemical
  47543. photochemical
  47544. initiation
  47545. radical
  47546. cyclization
  47547. aldol
  47548. photocycloaddition
  47549. photocycloadditions
  47550. photoinduced
  47551. photolysis
  47552. photolysis
  47553. sterically
  47554. hindered
  47555. aryloxy
  47556. phosphine
  47557. photooxygenation
  47558. photoproduct
  47559. photosensitization
  47560. photostimulated
  47561. phseoh
  47562. phseseph
  47563. phsih3
  47564. phso2
  47565. phthalimide
  47566. phthalimido
  47567. picolinic
  47568. pictet
  47569. phenyliodine
  47570. bistrifluoroacetate
  47571. pillared
  47572. pimarolide
  47573. pinacol
  47574. pinacolborane
  47575. pivotal
  47576. place
  47577. placed
  47578. planar
  47579. plane
  47580. planes
  47581. plausible
  47582. plays
  47583. plenum
  47584. plenum
  47585. plenum
  47586. press
  47587. pocket
  47588. pocl3
  47589. polar
  47590. polarity
  47591. polarization
  47592. polarize
  47593. polifunctional
  47594. politech
  47595. polyalkylated
  47596. polyamine
  47597. polycycles
  47598. polyfunctional
  47599. polyfunctionalized
  47600. polyhydroxy
  47601. polyketide
  47602. polymer
  47603. polyolefin
  47604. polypropionate
  47605. polystyrene
  47606. hyrin
  47607. porphyrins
  47608. portion
  47609. position
  47610. positioned
  47611. positionhave
  47612. positions
  47613. possessed
  47614. possessing
  47615. possibility
  47616. possible
  47617. postulated
  47618. postulates
  47619. potassium
  47620. potential
  47621. potentially
  47622. powder
  47623. powderand
  47624. powerful
  47625. pp1065
  47626. prabh
  47627. practical
  47628. practically
  47629. prcho
  47630. precursor
  47631. precursors
  47632. predictable
  47633. predicted
  47634. predictions
  47635. predominantly
  47636. predominates
  47637. predominating
  47638. preference
  47639. preferences
  47640. preferential
  47641. preferentially
  47642. preferred
  47643. preforming
  47644. preliminary
  47645. prentice-hall
  47646. preparation
  47647. preparation
  47648. activated
  47649. copper
  47650. napth
  47651. preparations
  47652. preparative
  47653. prepared
  47654. presence
  47655. presented
  47656. presenting
  47657. presents
  47658. preservation
  47659. preserves
  47660. press
  47661. press
  47662. press
  47663. press
  47664. pressure
  47665. presumably
  47666. presumed
  47667. previous
  47668. previous
  47669. reports
  47670. shown
  47671. thermolysis
  47672. aromatic
  47673. previously
  47674. primarily
  47675. primary
  47676. principle
  47677. principles
  47678. probable
  47679. probably
  47680. probe
  47681. probed
  47682. procedure
  47683. procedures
  47684. proceed
  47685. proceed
  47686. proceeded
  47687. proceeding
  47688. proceeds
  47689. proceeds
  47690. through
  47691. carbene
  47692. intermediate
  47693. proceeds
  47694. through
  47695. organoaluminum
  47696. species
  47697. which
  47698. oxidized
  47699. process
  47700. processes
  47701. processing
  47702. prochiral
  47703. produce
  47704. produced
  47705. produces
  47706. producing
  47707. product
  47708. products
  47709. a-hydroxy
  47710. amides
  47711. reduc
  47712. productsis
  47713. productwas
  47714. professional
  47715. professional/chapman
  47716. progressive
  47717. promote
  47718. promoted
  47719. promotes
  47720. promotion
  47721. pronounced
  47722. propadienyl
  47723. propan
  47724. propane
  47725. propanes
  47726. propanol
  47727. propargyl
  47728. propargylations
  47729. propargylic
  47730. propargylic
  47731. silanes
  47732. 24911
  47733. undergo
  47734. smooth
  47735. propen
  47736. propene
  47737. propenes
  47738. propenoates
  47739. propenyl
  47740. proper
  47741. properties
  47742. propionic
  47743. proportion
  47744. proposal
  47745. proposed
  47746. propynoate
  47747. propynyl
  47748. prostaglandins
  47749. protease
  47750. protected
  47751. protected
  47752. protecting
  47753. protecting/radicaltr
  47754. protectinggroup
  47755. protection
  47756. protective
  47757. protic
  47758. protocol
  47759. protodesilylation
  47760. proton
  47761. protonated
  47762. protonation
  47763. prototropy
  47764. proved
  47765. proven
  47766. provide
  47767. provided
  47768. provides
  47769. prudent
  47770. pseudo-13-diaxial
  47771. pseudo-axial
  47772. pseudoguaianolides
  47773. publications
  47774. published
  47775. publishers
  47776. publishers
  47777. pulegone
  47778. pummerer
  47779. pummerer
  47780. cyclization
  47781. aminoethyl
  47782. sulfoxide
  47783. pummerer
  47784. derived
  47785. substituted
  47786. vinylthionium
  47787. allyl
  47788. phenyl
  47789. purification
  47790. purities
  47791. purity
  47792. putative
  47793. puzzling
  47794. pyramidalization
  47795. pyranose
  47796. pyrazoles
  47797. pyrazoline
  47798. pyrazolines
  47799. pyrex
  47800. pyridin
  47801. pyridine
  47802. pyridinium
  47803. pyrido
  47804. pyridone
  47805. pyridones
  47806. pyridyl
  47807. pyridylthioesters
  47808. pyrimidones
  47809. pyrolysis
  47810. pyrolytic
  47811. pyrone
  47812. pyrophosphoryl
  47813. pyrrol
  47814. pyrrole
  47815. pyrroles
  47816. pyrrolidine
  47817. pyrrolidines
  47818. pyrrolidone
  47819. pyrrolin
  47820. pyrrolines
  47821. pyrrolizidine
  47822. pyrrolizine
  47823. pyrrolo
  47824. qualitative
  47825. qualitatively
  47826. quantify
  47827. quantitative
  47828. quantitatively
  47829. quantities
  47830. quarternary
  47831. quasi
  47832. quassinoids
  47833. quaternary
  47834. quench
  47835. quench
  47836. ketone
  47837. aldehyde
  47838. isocyanate
  47839. methyl
  47840. sulfonate
  47841. quenched
  47842. quenching
  47843. question
  47844. quinazolin
  47845. quinic
  47846. quinic
  47847. converted
  47848. stereoselectively
  47849. common
  47850. quinidine
  47851. quinine
  47852. quinodimethanes
  47853. quinoline
  47854. quinolinequinone
  47855. quinolinetriones
  47856. quinolones
  47857. quinone
  47858. quintuple
  47859. quinuclidine
  47860. ethyl
  47861. n-propyl
  47862. i-propyl
  47863. ch2ch2oh
  47864. using
  47865. grigg
  47866. tetrahedron
  47867. 464003
  47868. 2-no2
  47869. compound
  47870. noyori
  47871. angew
  47872. 198423847
  47873. other
  47874. hindered
  47875. containing
  47876. functionality
  47877. pronounced
  47878. asymmetric
  47879. induction
  47880. observed
  47881. during
  47882. r'ch2cl
  47883. r-oxazaborolidine
  47884. independently
  47885. co2me
  47886. co2me
  47887. co2me
  47888. r2alcl
  47889. r2alcl
  47890. coordinated
  47891. methacryloylsultam
  47892. undergoes
  47893. efficie
  47894. co2me
  47895. c-hexyl
  47896. 2-furyl
  47897. octyl
  47898. racemic
  47899. racemization
  47900. radical
  47901. radical
  47902. radicals
  47903. radicalsadjacent
  47904. radicalsto
  47905. raised
  47906. rakes
  47907. ramberg
  47908. range
  47909. ranged
  47910. ranges
  47911. ranging
  47912. rapid
  47913. rapid
  47914. metal
  47915. halogen
  47916. exchange
  47917. reactions
  47918. rapidly
  47919. acceleration
  47920. thermal
  47921. reaction
  47922. rather
  47923. ratio
  47924. ratio
  47925. 5a/5d/5b/5c
  47926. isomer
  47927. studied
  47928. ratio's
  47929. ratio's
  47930. felkin/anti-felkin
  47931. rationale
  47932. rationalise
  47933. rationalized
  47934. ratios
  47935. rayonet
  47936. rconhso2cl
  47937. reach
  47938. reaching
  47939. react
  47940. reactants
  47941. reacted
  47942. reacted
  47943. reacting
  47944. reaction
  47945. reaction
  47946. reaction
  47947. tosyl
  47948. derivative
  47949. phenylalaninol
  47950. reaction
  47951. diacetyl
  47952. hexen
  47953. dione
  47954. alkyl
  47955. reaction
  47956. acetoxy
  47957. azetidinone
  47958. crotylbromide
  47959. reaction
  47960. allylzirconation
  47961. products
  47962. alkynes
  47963. allyl
  47964. reaction
  47965. chiral
  47966. allylic
  47967. dienylic
  47968. cyclic
  47969. carbonates
  47970. reaction
  47971. different
  47972. vinyl
  47973. bromides
  47974. beating
  47975. phenyl
  47976. reaction
  47977. mesylcyanohydrins
  47978. furanos
  47979. ulose
  47980. reaction
  47981. subtituted
  47982. methylenecyclopropyl
  47983. ketones
  47984. reaction
  47985. serine
  47986. derived
  47987. reagent
  47988. acryloy
  47989. reaction
  47990. methylenecyclopropyl
  47991. reagent
  47992. couples
  47993. reaction
  47994. theoxabicylic
  47995. akene
  47996. dibal
  47997. reaction
  47998. proceeds
  47999. stereospecifically
  48000. suprafacial
  48001. manner
  48002. reaction
  48003. scope
  48004. synthesis
  48005. membered
  48006. cyclic
  48007. reactions
  48008. reactions
  48009. bromo
  48010. phenylacetic
  48011. acids
  48012. reactions
  48013. diaryl
  48014. dithiolium
  48015. salts
  48016. alkali
  48017. reactions
  48018. molybdenum
  48019. stabilized
  48020. propargyl
  48021. cations
  48022. reactions
  48023. pyrophosphoryl
  48024. chloride
  48025. amides
  48026. derived
  48027. reactivity
  48028. structure
  48029. concepts
  48030. organic
  48031. chemistry
  48032. reactor
  48033. reacts
  48034. readily
  48035. reagent
  48036. reagents
  48037. realised
  48038. realized
  48039. rearangement
  48040. rearrange
  48041. rearranged
  48042. rearrangement
  48043. asonable
  48044. recent
  48045. recent
  48046. developements
  48047. recently
  48048. receptors
  48049. recognition
  48050. recombination
  48051. recovered
  48052. reduced
  48053. reducing
  48054. reduction
  48055. works
  48056. tetrabutyl
  48057. ammonium
  48058. chloride
  48059. reduction
  48060. alkyl
  48061. trialkylsilyl
  48062. propenyl
  48063. methylcarbon
  48064. reduction
  48065. indolyldihydrodyridi
  48066. satisfactorily
  48067. reduction
  48068. ketimine
  48069. itsuno's
  48070. reagent
  48071. reductions
  48072. reductive
  48073. reductive
  48074. cleavage
  48075. geminal
  48076. phenylsulfones
  48077. using
  48078. lithi
  48079. merlic
  48080. 1991113
  48081. nakamura
  48082. luche
  48083. references
  48084. reflects
  48085. reflux
  48086. refluxing
  48087. regards
  48088. regenerates
  48089. regio
  48090. regio
  48091. regiochemical
  48092. regiochemistry
  48093. regiocontrol
  48094. regioisomer
  48095. regioisomeric
  48096. regioselective
  48097. regioselectivechloro
  48098. regioselectively
  48099. regioselectivities
  48100. regioselectivity
  48101. regiospecific
  48102. fluorination
  48103. using
  48104. fluorobenzenesulfoni
  48105. regiospecifically
  48106. regiospecificity
  48107. reinhold
  48108. reinvestigated
  48109. related
  48110. relative
  48111. relatively
  48112. remainder
  48113. remained
  48114. remains
  48115. remarkable
  48116. remarkably
  48117. remote
  48118. remotely
  48119. removal
  48120. removal
  48121. either
  48122. phsih3
  48123. cf3con
  48124. sime3
  48125. remove
  48126. removed
  48127. replaced
  48128. report
  48129. reported
  48130. reported
  48131. reports
  48132. representative
  48133. representing
  48134. represents
  48135. reproduce
  48136. reproduces
  48137. required
  48138. requisite
  48139. resin
  48140. resolution
  48141. respect
  48142. respective
  48143. respectively
  48144. result
  48145. result
  48146. yield
  48147. resultant
  48148. resulted
  48149. resulting
  48150. results
  48151. retention
  48152. reused
  48153. reveal
  48154. revealed
  48155. reveals
  48156. reveiw
  48157. reversal
  48158. review
  48159. comprehensive
  48160. organic
  48161. synthesis
  48162. review
  48163. comprehensive
  48164. organic
  48165. synthesis
  48166. trost
  48167. review
  48168. saccomano
  48169. comprehensive
  48170. organic
  48171. synthesis
  48172. review
  48173. paper
  48174. emphasis
  48175. removal
  48176. reviews
  48177. reviews
  48178. denmark
  48179. organic
  48180. reactions
  48181. paquette
  48182. revises
  48183. revision
  48184. rgamon
  48185. rh/al2o3
  48186. rhamnal
  48187. rhodium
  48188. rhodium
  48189. acetate
  48190. catalysed
  48191. decomposition
  48192. phenyldiaz
  48193. rhodium
  48194. carboxylate
  48195. catalysed
  48196. decomposition
  48197. diazo
  48198. ribofuranose
  48199. ribofuranosides
  48200. ribonolactone
  48201. right
  48202. selectivity
  48203. diels
  48204. alder
  48205. reactions
  48206. naphthazarin
  48207. rings
  48208. ritter
  48209. ropriate
  48210. rotate
  48211. rotation
  48212. route
  48213. routes
  48214. royal
  48215. royal
  48216. sociaty
  48217. chemistry
  48218. royal
  48219. society
  48220. mistry
  48221. royal
  48222. society
  48223. chemistry
  48224. royal
  48225. society
  48226. chemistry
  48227. rstips
  48228. rucl2
  48229. rucl2
  48230. excellent
  48231. catalyst
  48232. olefin
  48233. hydrogenati
  48234. ruthenium
  48235. ruthenium
  48236. trichloride
  48237. sodium
  48238. periodate
  48239. highly
  48240. efficient
  48241. salts
  48242. samarium
  48243. samarium
  48244. iodide
  48245. mediated
  48246. closures
  48247. substituted
  48248. samarium
  48249. iodide
  48250. mediated
  48251. closures
  48252. substituted
  48253. sandwich
  48254. satisfactorily
  48255. satisfactory
  48256. scaled
  48257. scandium
  48258. scanning
  48259. scheme
  48260. schollkopf's
  48261. schuster
  48262. science
  48263. science
  48264. scientific
  48265. scission
  48266. scope
  48267. search
  48268. seated
  48269. secodaphniphylline
  48270. second
  48271. second
  48272. yield
  48273. secondary
  48274. secondaryamino
  48275. secure
  48276. davies
  48277. tetrahedron
  48278. asymmetry
  48279. similar
  48280. following
  48281. paper
  48282. babiak
  48283. watanabe
  48284. synlett
  48285. 1993115
  48286. curran
  48287. tetrahedron
  48288. review
  48289. following
  48290. article
  48291. previous
  48292. papers
  48293. following
  48294. papers
  48295. selective
  48296. protection
  48297. carbohy
  48298. seeman
  48299. seems
  48300. selctive
  48301. selection
  48302. selective
  48303. selective
  48304. activation
  48305. ester
  48306. bidentate
  48307. complexat
  48308. selective
  48309. functionalisation
  48310. chlorimine
  48311. group
  48312. selectivechlorinatio
  48313. selectively
  48314. selectivities
  48315. selectivity
  48316. reaction
  48317. decreases
  48318. increased
  48319. reaction
  48320. selectride
  48321. selena
  48322. selenium
  48323. seleno
  48324. semiempirical
  48325. semisynthetic
  48326. sensitive
  48327. separated
  48328. separation
  48329. sequence
  48330. sequential
  48331. series
  48332. serine
  48333. serine
  48334. sertraline
  48335. served
  48336. serves
  48337. sesquiterpne
  48338. seven
  48339. several
  48340. several
  48341. carboxylate
  48342. group
  48343. receptors
  48344. several
  48345. procedures
  48346. which
  48347. based
  48348. zirconium
  48349. catalyze
  48350. several
  48351. sulfides
  48352. converted
  48353. sulfoxides
  48354. sulfon
  48355. several
  48356. title
  48357. compounds
  48358. containing
  48359. aldehyde
  48360. ketone
  48361. unsatu
  48362. sevier
  48363. shielding
  48364. shift
  48365. shiftswill
  48366. shigeru
  48367. shigeru
  48368. tokyo
  48369. japan
  48370. short
  48371. short
  48372. review
  48373. shorter
  48374. should
  48375. showed
  48376. shown
  48377. shown
  48378. sidechains
  48379. sieves
  48380. sigma
  48381. sigmatropic
  48382. signals
  48383. significant
  48384. significantly
  48385. silane
  48386. silanes
  48387. silica
  48388. silicon
  48389. siliyl
  48390. siloxy
  48391. silver
  48392. silyl
  48393. silylated
  48394. silylating
  48395. silylation
  48396. silylenol
  48397. silyloxy
  48398. silyloxydienes
  48399. sime3
  48400. similar
  48401. simple
  48402. simplicity
  48403. simultaneous
  48404. since
  48405. single
  48406. singlet
  48407. sings
  48408. sites
  48409. situated
  48410. examples
  48411. varying
  48412. nucleophiles
  48413. yields
  48414. 43-86
  48415. examples
  48416. yields
  48417. ratios
  48418. skeletones
  48419. slightly
  48420. small
  48421. mediates
  48422. reductive
  48423. addition
  48424. geminal
  48425. presents
  48426. catalytic
  48427. activity
  48428. diels
  48429. alder
  48430. reactions
  48431. smi2/hmpt
  48432. smooth
  48433. smoothly
  48434. snbr4
  48435. sncl4
  48436. snsime
  48437. so2cl2
  48438. sociaty
  48439. society
  48440. socl2
  48441. sodium
  48442. sodium
  48443. sodium
  48444. borohydride
  48445. reduction
  48446. alpha
  48447. nitrocycloalkanones
  48448. solid
  48449. solution
  48450. solutions
  48451. solvent
  48452. solvent
  48453. solvent
  48454. either
  48455. dichloroethane
  48456. benzene
  48457. solvents
  48458. solvolysis
  48459. sonochemical
  48460. sorbate
  48461. sosnovsky
  48462. source
  48463. specific
  48464. specifically
  48465. spectrometry
  48466. spectroscopy
  48467. speed
  48468. spengler
  48469. spiro
  48470. spiro
  48471. undecane
  48472. derivatives
  48473. obtained
  48474. spiroannelation
  48475. spiroconjugation
  48476. spirocyclic
  48477. spirodienone
  48478. spiroketal
  48479. spiroketals
  48480. spiroorthocarbonic
  48481. spiroorthocarboxylic
  48482. spiropentanopyrroliz
  48483. sponge
  48484. spontaneously
  48485. springer
  48486. springer
  48487. verlag
  48488. springer-verlag
  48489. springer-verlag
  48490. berlin
  48491. springerverlag
  48492. stability
  48493. stabilityof
  48494. stabilization
  48495. stabilize
  48496. stabilized
  48497. stabilizing
  48498. stable
  48499. stannane
  48500. stannanes
  48501. stannes
  48502. stannous
  48503. stannyl
  48504. stannylacrylates
  48505. stannylpropionates
  48506. starling
  48507. starting
  48508. starting
  48509. starting
  48510. chiral
  48511. mercapto
  48512. alcohols
  48513. several
  48514. reaction
  48515. starting
  48516. corresponding
  48517. indoles
  48518. indole
  48519. acetic
  48520. starts
  48521. state
  48522. states
  48523. steps
  48524. stereocenter
  48525. stereocenters
  48526. stereochemical
  48527. stereochemistries
  48528. stereochemistry
  48529. stereochemistry
  48530. generation
  48531. lithium
  48532. zincate
  48533. carbeno
  48534. stereocontrol
  48535. stereocontrolled
  48536. stereocontrolling
  48537. stereodefined
  48538. stereodifferentiatin
  48539. stereoelectronic
  48540. stereogenesis
  48541. stereogenic
  48542. stereoinduction
  48543. stereoisomeric
  48544. stereomer
  48545. stereoselective
  48546. stereoselective
  48547. preparation
  48548. acyclic
  48549. alpha
  48550. azidoaldehyd
  48551. stereoselectiveintro
  48552. stereoselectively
  48553. stereoselectivities
  48554. stereoselectivity
  48555. stereospecific
  48556. stereospecific
  48557. annulation
  48558. cyclic
  48559. alkenes
  48560. preparat
  48561. stereospecifically
  48562. steric
  48563. stericallycrowded
  48564. steroidal
  48565. stilbenes
  48566. still
  48567. still
  48568. 1977994836
  48569. stille
  48570. stiochiometric
  48571. stiochiometric
  48572. palladium
  48573. stirred
  48574. stirring
  48575. stoichiometric
  48576. story
  48577. straight
  48578. strained
  48579. strategy
  48580. strong
  48581. stronger
  48582. strongly
  48583. structural
  48584. structurally
  48585. structure
  48586. structures
  48587. strychnos
  48588. studied
  48589. studies
  48590. study
  48591. study
  48592. preference
  48593. insertion
  48594. tertiary
  48595. studying
  48596. styrene
  48597. styrenes
  48598. styryl
  48599. suarez
  48600. subject
  48601. subjected
  48602. subsequent
  48603. subsequently
  48604. substates
  48605. substituent
  48606. substituent
  48607. substituents
  48608. substituted
  48609. substitutents
  48610. substitution
  48611. substoichiometric
  48612. substrate
  48613. substrates
  48614. successful
  48615. successfully
  48616. successive
  48617. successive
  48618. thermal
  48619. reactions
  48620. based
  48621. claisen
  48622. overm
  48623. successively
  48624. succinimide
  48625. sufenylimidate
  48626. sufficiently
  48627. sugar
  48628. suggest
  48629. suggested
  48630. suggesting
  48631. suggestion
  48632. suggests
  48633. suitable
  48634. suitably
  48635. sulfate
  48636. sulfenamides
  48637. sulfenates
  48638. sulfenic
  48639. sulfenylation
  48640. sulfide
  48641. sulfides
  48642. sulfinyl
  48643. sulfolene
  48644. sulfonamide
  48645. sulfonate
  48646. sulfonates
  48647. sulfone
  48648. sulfones
  48649. sulfonium
  48650. sulfonyl
  48651. sulfoxide
  48652. sulfoxides
  48653. sulfur
  48654. sulfuryl
  48655. sulphamidate
  48656. sulphides
  48657. sulphone
  48658. sultam
  48659. super
  48660. supercritical
  48661. support
  48662. supported
  48663. suppress
  48664. suprafacial
  48665. nidine
  48666. surprisingly
  48667. surrounding
  48668. swern
  48669. symmetric
  48670. symmetrical
  48671. syn/anti
  48672. ratio
  48673. dependent
  48674. lewis
  48675. synclinal
  48676. synlett
  48677. syntheses
  48678. syntheses
  48679. substituted
  48680. hydroxyethylene
  48681. building
  48682. blocks
  48683. synthesis
  48684. membered
  48685. rings
  48686. synthesis
  48687. dynemicin
  48688. model
  48689. synthesis
  48690. homoallylic
  48691. amines
  48692. synthesis
  48693. pimarolide
  48694. methylester
  48695. syn/anti
  48696. ratio
  48697. dependent
  48698. lewis
  48699. acid@
  48700. synthesis
  48701. membered
  48702. rings@
  48703. synthesis
  48704. complex
  48705. binol
  48706. added
  48707. systematic@
  48708. tandem
  48709. temperatures@
  48710. terminus@
  48711. tetrahedron1987@
  48712. tetramethylpiperdine@
  48713. correspondi@
  48714. direct
  48715. oxidation
  48716. alpha
  48717. alkoxyalkyl
  48718. trialkylstannanes
  48719. intrinsic
  48720. stereoselectivity
  48721. cyanide
  48722. addition
  48723. tobe@
  48724. novel
  48725. alkyllithium
  48726. intriguingly
  48727. stabletow@
  48728. presence
  48729. methanol
  48730. greatly
  48731. accelerates
  48732. reaction@
  48733. reaction
  48734. ethyl
  48735. dimethylamino
  48736. penta
  48737. dienoate
  48738. scope
  48739. tandem
  48740. radical
  48741. mediated
  48742. macrocyclisation
  48743. trans@
  48744. structures
  48745. novel
  48746. spiropentanopyrroliz
  48747. oxime
  48748. alkal@
  48749. trifluoromethylation
  48750. aldehydes
  48751. ketones
  48752. trifl@
  48753. thermodynamical
  48754. thieme
  48755. titanium
  48756. trans
  48757. synthesis
  48758. complex
  48759. binol
  48760. added
  48761. synthesis
  48762. cis-tetrahydropyran
  48763. given
  48764. synthesis
  48765. starting
  48766. material
  48767. accomplished
  48768. using
  48769. synthesis
  48770. tropane
  48771. alkaloids
  48772. darlingine
  48773. chalcostrobamine
  48774. synthesis
  48775. vinblastine
  48776. synthesised
  48777. synthesize
  48778. synthesized
  48779. synthetic
  48780. synthetic
  48781. studies
  48782. angucycline
  48783. antiobiotics
  48784. stereocont
  48785. synthetically
  48786. synthon
  48787. synthons
  48788. system
  48789. ishii
  48790. t-butyl
  48791. t-butylamine
  48792. t-butylamine
  48793. taddol
  48794. takes
  48795. tandem
  48796. tandem
  48797. tandem
  48798. nitrone
  48799. generation/cycloaddi
  48800. reactions
  48801. between
  48802. simple
  48803. target
  48804. tautomer
  48805. tautomers
  48806. taxane
  48807. taxoid
  48808. taxol
  48809. taxol
  48810. prepared
  48811. yield
  48812. coupling
  48813. oxazol
  48814. tazettine
  48815. tbdms
  48816. tbdmsotf
  48817. tbdps
  48818. tdmpp
  48819. super
  48820. hydride
  48821. produces
  48822. telluride
  48823. added
  48824. neutralize
  48825. phseoh
  48826. formed
  48827. during
  48828. technique
  48829. techniques
  48830. telluride
  48831. tellurium
  48832. reaction
  48833. ranges
  48834. temperatre
  48835. temperature
  48836. terminal
  48837. olefins
  48838. terminally
  48839. terminator
  48840. terminus
  48841. terms
  48842. terphenyls
  48843. tertiary
  48844. tertiary
  48845. amines
  48846. intramolecular
  48847. nucleophile
  48848. tertiary
  48849. propargylic
  48850. alcohols
  48851. reacted
  48852. carbon
  48853. monoxide
  48854. tested
  48855. tether
  48856. tethered
  48857. tethers
  48858. tetra
  48859. tetraamine
  48860. tetrabutyl
  48861. tetrabutylammonium
  48862. tetrachloride
  48863. tetracoordinated
  48864. tetracoordination
  48865. tetracyclic
  48866. tetraene
  48867. tetrafluorothiopheno
  48868. tetrahedron
  48869. tetrahedron
  48870. tetrahydro
  48871. tetrahydrofuran
  48872. tetrahydrofurans
  48873. tetrahydromevinic
  48874. tetrahydropyran
  48875. tetrahydropyrans
  48876. tetrahydropyranyl
  48877. tetrahydropyridines
  48878. tetrahydropyridinium
  48879. tetrakis
  48880. tetramethylindan
  48881. tetramethylpiperdine
  48882. tetramethylpiperidin
  48883. tetraoxadispiro
  48884. tetraphenyl
  48885. tetraphenylbut
  48886. tetraphenylcyclopent
  48887. tetrasubstituted
  48888. tetrasulfides
  48889. tetroxide
  48890. thatachieved
  48891. thatthis
  48892. wittig
  48893. rearrangements
  48894. enantio
  48895. defined
  48896. benzyloxyp
  48897. oxonia
  48898. rearrangement
  48899. shown
  48900. importan
  48901. ester
  48902. group
  48903. protected
  48904. diethyl
  48905. aspartate
  48906. approach
  48907. synthesis
  48908. tetracyclic
  48909. above
  48910. aldehyde
  48911. prepared
  48912. asymmetric
  48913. aldol
  48914. absence
  48915. zncl2
  48916. causes
  48917. reversal
  48918. selectivity
  48919. addition
  48920. camphorsulfonic
  48921. additions
  48922. various
  48923. organometallic
  48924. species
  48925. oxabicy
  48926. aldol
  48927. reactions
  48928. subsequent
  48929. transmetallation
  48930. alkoxy
  48931. radicals
  48932. formed
  48933. reaction
  48934. steroidal
  48935. alkyl
  48936. vinyl
  48937. ethers
  48938. deriving
  48939. alcohols
  48940. alkylation
  48941. symmetric
  48942. aminoaziridinylhydra
  48943. anion
  48944. alkylation
  48945. monolithium
  48946. derived
  48947. chloromethy
  48948. analogue
  48949. cephalotaxine
  48950. skeleton
  48951. prepared
  48952. nitrile
  48953. which
  48954. advanced
  48955. intermediate
  48956. barton
  48957. esters
  48958. synthesized
  48959. correspondi
  48960. benzylic
  48961. group
  48962. removed
  48963. barton
  48964. deoxygenation
  48965. hydroxyl
  48966. group
  48967. rhamnal
  48968. glucal
  48969. underwe
  48970. cascade
  48971. cycloaddition
  48972. alkoxycyclohexadieno
  48973. catalytic
  48974. asymmetric
  48975. cycloaddition
  48976. proceeds
  48977. between
  48978. chiral
  48979. lewis
  48980. prepared
  48981. binaphthol
  48982. diisopr
  48983. construction
  48984. cycloalkyl
  48985. alpha
  48986. position
  48987. cyclization
  48988. hexen
  48989. radicals
  48990. cycloaddition
  48991. reactions
  48992. three
  48993. cyclic
  48994. imidate
  48995. esters
  48996. cyclopentapyranones
  48997. representing
  48998. fused
  48999. derivatives
  49000. trans
  49001. bicyclo
  49002. 3.3.0
  49003. octane
  49004. diazoester
  49005. prepared
  49006. corresponding
  49007. ester
  49008. diethylisopropylsily
  49009. ether
  49010. deips
  49011. selectively
  49012. cleaved
  49013. dimethyldioxirane
  49014. oxidations
  49015. allenic
  49016. amine
  49017. derivative
  49018. corresponding
  49019. above
  49020. substates
  49021. provides
  49022. direct
  49023. oxidation
  49024. alpha
  49025. alkoxyalkyl
  49026. trialkylstannanes
  49027. selectivity
  49028. introduction
  49029. substitut
  49030. efficient
  49031. rapid
  49032. alpha
  49033. gamma
  49034. rearrangement
  49035. enantioselective
  49036. addition
  49037. diethylzinc
  49038. aldehydes
  49039. dibromo
  49040. oxanorborneno
  49041. succinimide
  49042. first
  49043. enantioselective
  49044. version
  49045. ester
  49046. enolate
  49047. first
  49048. report
  49049. metalated
  49050. diazomethane
  49051. eugen
  49052. muller
  49053. formation
  49054. substituted
  49055. bicycle
  49056. 3.2.0
  49057. fragmentation
  49058. nitrate
  49059. ester
  49060. alkoxy
  49061. radical
  49062. highly
  49063. stereoselective
  49064. hydride
  49065. reductions
  49066. chiral
  49067. ch3cn
  49068. complex
  49069. directly
  49070. passing
  49071. fluorine
  49072. hydroboration
  49073. alkenes
  49074. catecholborane
  49075. reaction
  49076. novel
  49077. hypervalent
  49078. iodine
  49079. reagent
  49080. intermediate
  49081. contains
  49082. aromatic
  49083. bromine
  49084. posit
  49085. intramolecular
  49086. diels
  49087. alder
  49088. reactions
  49089. series
  49090. intrinsic
  49091. stereoselectivity
  49092. cyanide
  49093. addition
  49094. ionic
  49095. reduction
  49096. variety
  49097. stannylacrylates
  49098. reaction
  49099. efficiently
  49100. construct
  49101. isoxazolines
  49102. obtained
  49103. nitrile
  49104. oxide
  49105. kinetic
  49106. resolution
  49107. racemic
  49108. alkoxy
  49109. furanones
  49110. level
  49111. diastereoselectivity
  49112. depends
  49113. lifetime
  49114. triplet
  49115. cyclopropylcyclopent
  49116. manganese
  49117. initiated
  49118. oxidative
  49119. radical
  49120. reaction
  49121. mechanism
  49122. involve
  49123. membered
  49124. cyclic
  49125. intermediate
  49126. mechanism
  49127. epoxidation
  49128. chiral
  49129. allyl
  49130. amines
  49131. michael
  49132. initiated
  49133. closure
  49134. reaction
  49135. explore
  49136. mitsunobu
  49137. azide
  49138. modification
  49139. studied
  49140. mitsunobu
  49141. reaction
  49142. synthesis
  49143. mitsunobu
  49144. reaction
  49145. tyrosine
  49146. methyl
  49147. ether
  49148. chiral
  49149. methoxyacetic
  49150. acids
  49151. prepared
  49152. novel
  49153. alkyllithium
  49154. intriguingly
  49155. stabletow
  49156. iodoanilide
  49157. group
  49158. shown
  49159. broadly
  49160. useful
  49161. forthe
  49162. optically
  49163. active
  49164. methyl
  49165. benzyltetracyclic
  49166. ketone
  49167. original
  49168. cf3sime3
  49169. carbon
  49170. nitrogen
  49171. double
  49172. palladium
  49173. catalysed
  49174. reaction
  49175. vinyl
  49176. halides
  49177. palladium
  49178. catalyzed
  49179. carbonylation
  49180. methoxycarbonyl
  49181. palladium
  49182. catalyzed
  49183. cross
  49184. coupling
  49185. reaction
  49186. arylhalid
  49187. palladium
  49188. catalyzed
  49189. reaction
  49190. tosyl
  49191. tributylstanny
  49192. palladium
  49193. catalyzed
  49194. vicinal
  49195. carbonylation
  49196. subst
  49197. palladium
  49198. catalyzed
  49199. cross
  49200. coupling
  49201. reaction
  49202. phenylthio
  49203. group
  49204. phenylthioazetidinon
  49205. readily
  49206. pheomelanin
  49207. precursor
  49208. related
  49209. dihydro
  49210. photocycloaddition
  49211. unsymmetrically
  49212. substituted
  49213. alkene
  49214. photostimulated
  49215. reaction
  49216. iodobicyclo
  49217. 4.1.0
  49218. heptane
  49219. preparation
  49220. enantiomerically
  49221. lithio
  49222. dioxola
  49223. presence
  49224. methanol
  49225. greatly
  49226. accelerates
  49227. reaction
  49228. presence
  49229. water
  49230. determining
  49231. efficiency
  49232. principles
  49233. cyano
  49234. hydroxylation
  49235. olefins
  49236. products
  49237. stereochemistries
  49238. carbenic
  49239. decomposition
  49240. pummerer
  49241. reaction
  49242. acyclic
  49243. sulfoxides
  49244. silylated
  49245. radical
  49246. chain
  49247. addition
  49248. reaction
  49249. benzenethiol
  49250. allen
  49251. radical
  49252. cyclization
  49253. alkyl
  49254. enopyranosides
  49255. provid
  49256. reaction
  49257. between
  49258. substituted
  49259. enamines
  49260. phenylglyoxa
  49261. reaction
  49262. bromo
  49263. chloromethyl
  49264. methyltricyclo
  49265. reaction
  49266. acyclic
  49267. phosphoric
  49268. reaction
  49269. alkyl
  49270. sulfones
  49271. excess
  49272. reaction
  49273. alkynyl
  49274. boranes
  49275. generated
  49276. lithi
  49277. reaction
  49278. cerium
  49279. ceric
  49280. ammonium
  49281. nitrate
  49282. reaction
  49283. diazomethane
  49284. allene
  49285. temperature
  49286. reaction
  49287. dimethyl
  49288. benzylazetidin
  49289. propane
  49290. reaction
  49291. ethyl
  49292. dimethylamino
  49293. penta
  49294. dienoate
  49295. reaction
  49296. excess
  49297. dimethylsulphonium
  49298. methylide
  49299. reaction
  49300. excess
  49301. dimethylsulfonium
  49302. methylide
  49303. reaction
  49304. iodoesters
  49305. electrophilic
  49306. olefins
  49307. reaction
  49308. iodotrimethylsilane
  49309. sugar
  49310. lactones
  49311. reaction
  49312. oxazolopiperidones
  49313. oxazolopi
  49314. reaction
  49315. iodoacrylic
  49316. substoichiomet
  49317. reaction
  49318. dichlorobut
  49319. dichlor
  49320. reactions
  49321. ethoxybut
  49322. dimethylhydrazone
  49323. readily
  49324. available
  49325. symmetric
  49326. aziridines
  49327. regio
  49328. stereoselectivity
  49329. induced
  49330. addition
  49331. regioselective
  49332. lithiation
  49333. functionalization
  49334. regioselectivities
  49335. determined
  49336. alkylations
  49337. opening
  49338. reaction
  49339. diphenylphosphinoyla
  49340. coppe
  49341. axially
  49342. disposed
  49343. proposed
  49344. sulfur
  49345. scope
  49346. tandem
  49347. radical
  49348. mediated
  49349. macrocyclisation
  49350. trans
  49351. search
  49352. configurationally
  49353. stable
  49354. amino
  49355. carbanions
  49356. selective
  49357. alkylation
  49358. amides
  49359. cyclic
  49360. acyclic
  49361. under
  49362. selenium
  49363. induced
  49364. cyclization
  49365. substituted
  49366. hydroxy
  49367. unsaturated
  49368. nitrile
  49369. equilibrates
  49370. tempera
  49371. solid
  49372. phase
  49373. synthesis
  49374. peptides
  49375. incorporating
  49376. thesteri
  49377. sonochemical
  49378. promoted
  49379. aluminum
  49380. amalgam
  49381. reduction
  49382. source
  49383. asymmetric
  49384. induction
  49385. using
  49386. chiral
  49387. ligands
  49388. stereochemistry
  49389. dipolar
  49390. cycloaddition
  49391. methyl
  49392. stereoselective
  49393. cyclization
  49394. cyanoamine
  49395. containin
  49396. stereoselective
  49397. transmetallation
  49398. subsequent
  49399. alkylati
  49400. stereospecific
  49401. sequential
  49402. substitution
  49403. dichlo
  49404. stereospecific
  49405. synthesis
  49406. glycoprotein
  49407. processing
  49408. steroidal
  49409. alpha
  49410. alcohol
  49411. diacetoxyiodo
  49412. benzene
  49413. structural
  49414. revision
  49415. product
  49416. tandem
  49417. aldol
  49418. structures
  49419. novel
  49420. spiropentanopyrroliz
  49421. oxime
  49422. alkal
  49423. isomer
  49424. formed
  49425. reaction
  49426. epimeric
  49427. synthesis
  49428. diastereoselective
  49429. oxidation
  49430. novel
  49431. synthesis
  49432. mechanism
  49433. formation
  49434. purification
  49435. synthesis
  49436. crown
  49437. ether
  49438. enediyne
  49439. pallad
  49440. synthesis
  49441. functionalised
  49442. alkenylstannanes
  49443. synthesis
  49444. substituted
  49445. alpha
  49446. carbolines
  49447. descr
  49448. synthesis
  49449. aminobutanoic
  49450. starting
  49451. chiral
  49452. synthetic
  49453. potential
  49454. regio
  49455. stereoselectivity
  49456. titan
  49457. synthetic
  49458. usefulnes
  49459. method
  49460. triazole
  49461. synthetic
  49462. utility
  49463. generation
  49464. study
  49465. title
  49466. compound
  49467. obtained
  49468. steps
  49469. overall
  49470. title
  49471. compound
  49472. subjected
  49473. phase
  49474. pyrolysis
  49475. title
  49476. reaction
  49477. occurs
  49478. through
  49479. sequence
  49480. title
  49481. rearrangement
  49482. shown
  49483. proceed
  49484. trifluoromethylation
  49485. aldehydes
  49486. ketones
  49487. trifl
  49488. trimethylsilyl
  49489. analogue
  49490. gives
  49491. mixtures
  49492. olefin
  49493. triphenylphosphine
  49494. deoxygenation
  49495. dimethyllbenzofur
  49496. quinoline
  49497. units
  49498. located
  49499. parallel
  49500. planes
  49501. bisphosphine
  49502. ligands
  49503. related
  49504. chiral
  49505. related
  49506. bulky
  49507. titanium
  49508. alkoxides
  49509. configurated
  49510. enoltriflates
  49511. treated
  49512. zn/acoh
  49513. reduction
  49514. leads
  49515. carbonylreducti
  49516. theallyl
  49517. thebicyclic
  49518. thecorresponding
  49519. their
  49520. theme
  49521. cleophile
  49522. theoretical
  49523. theory
  49524. there
  49525. thereaction
  49526. therefore
  49527. theresulting
  49528. thermal
  49529. thermodynamical
  49530. thermolysis
  49531. thesame
  49532. these
  49533. thestereochemical
  49534. thesterically
  49535. thevinylcyclopropane
  49536. thiadiazole
  49537. thiadiazoles
  49538. thiazinone
  49539. thiazole
  49540. thiazolo
  49541. thieme
  49542. thieme
  49543. thieme
  49544. thieme
  49545. thienamycin
  49546. thietanes
  49547. thiiranes
  49548. thioacetals
  49549. thioacetates
  49550. thioacid
  49551. thioalkyl
  49552. thioalkylacetaldehyd
  49553. thioamide
  49554. thioanalogs
  49555. thiobenzoates
  49556. thiobenzophenone
  49557. thiobenzophenone
  49558. thiofluorenone
  49559. dienophil
  49560. thiocarbamate
  49561. thiocarbonyl
  49562. thiocarboxylates
  49563. thiochroman
  49564. thiochroman
  49565. diones
  49566. which
  49567. result
  49568. reaction
  49569. ofthioc
  49570. thioderivatives
  49571. thioester
  49572. thioesters
  49573. thiofluorenone
  49574. thioimidates
  49575. thiol
  49576. thiolactam
  49577. thiolate
  49578. thiolated
  49579. thiolmide
  49580. thiols
  49581. thione
  49582. thiones
  49583. thionyl
  49584. thiophene
  49585. thiophenes
  49586. thiophenoxide
  49587. thiopyran
  49588. thiopyridines
  49589. thiosubstituted
  49590. thirty
  49591. rowave
  49592. techniques
  49593. method
  49594. avoids
  49595. reduction
  49596. olefins
  49597. acetylenes
  49598. keton
  49599. method
  49600. suitable
  49601. aliphatic
  49602. glycidic
  49603. esters
  49604. reaction
  49605. occurs
  49606. stepwise
  49607. mechanism
  49608. afford
  49609. thisselectivity
  49610. thiyl
  49611. those
  49612. though
  49613. three
  49614. threo
  49615. through
  49616. tibr4
  49617. ticl2
  49618. ticl4
  49619. tight
  49620. times
  49621. tioac
  49622. tipscl
  49623. tishchenko
  49624. titanium
  49625. titanium
  49626. titlecompound
  49627. tmeda
  49628. tms-cn
  49629. tms-n3
  49630. tmscl
  49631. tmscn
  49632. tmsoff
  49633. tmsotf
  49634. tobeta
  49635. toformic
  49636. togive
  49637. tokyo
  49638. tolerant
  49639. tolerates
  49640. toluene
  49641. toluenesulfonate
  49642. toluenesulphonate
  49643. toluenesunonhydrazid
  49644. toluyl
  49645. tolyloxyfuran
  49646. tolylsulfenyl
  49647. tolylsulfinyl
  49648. tolylsulfonyl
  49649. torsional
  49650. tosyl
  49651. tosylate
  49652. tosylates
  49653. tosylmethyl
  49654. tosyloxy
  49655. tosylpropene
  49656. tosyltrimethylsilane
  49657. total
  49658. erythronolide
  49659. steps
  49660. total
  49661. total
  49662. synthesis
  49663. secodaphniphylline
  49664. total
  49665. synthesis
  49666. oliogosaccharide
  49667. fragment
  49668. calichea
  49669. totally
  49670. toward
  49671. towards
  49672. towards
  49673. synthesis
  49674. nikkomycin
  49675. toxic
  49676. trace
  49677. traditional
  49678. tranfer
  49679. trans
  49680. trans
  49681. trans
  49682. epoxide
  49683. yield
  49684. trans/cis
  49685. transannulation
  49686. transesterification
  49687. transfer
  49688. transfers
  49689. transformation
  49690. transformations
  49691. transformed
  49692. transfused
  49693. transient
  49694. transition
  49695. decomposition
  49696. diazoesters
  49697. transition
  49698. structures
  49699. wittig
  49700. rearrangements
  49701. allylox
  49702. transition-state
  49703. translocation
  49704. transmetalated
  49705. transmetallation
  49706. transmissive
  49707. transposition
  49708. trapped
  49709. trapping
  49710. treated
  49711. treatment
  49712. treatment
  49713. butyldimethylsilyl
  49714. triethylsilyloxymet
  49715. treatment
  49716. nitrobicyclo
  49717. 2.2.1
  49718. treatment
  49719. triethylsilyl
  49720. hydroxy
  49721. deacetylbaccati
  49722. treatment
  49723. appropriately
  49724. substituted
  49725. diene
  49726. triene
  49727. treatment
  49728. allyl
  49729. ethers
  49730. catalytic
  49731. amounts
  49732. treatment
  49733. stannyl
  49734. aldehydes
  49735. ketone
  49736. treatment
  49737. acetylenic
  49738. epoxides
  49739. having
  49740. electron
  49741. donat
  49742. treatment
  49743. iodotrienone
  49744. bu3snh
  49745. results
  49746. tri-substituted
  49747. triads
  49748. trialkylphosphonoace
  49749. trialkylsilyl
  49750. trialkylstannanes
  49751. triazole
  49752. triazoles
  49753. triazolium
  49754. triazolyl
  49755. tributyl
  49756. tributylallenyl
  49757. tributylstannane
  49758. tributylstannyl
  49759. tributyltin
  49760. trichloride
  49761. tricthylamine
  49762. tricycle
  49763. tricyclic
  49764. tricyclo
  49765. treatment
  49766. butyldimethylsilyl
  49767. triethylsilyloxymet@
  49768. tricyclooctanones@
  49769. triflic@
  49770. trimethylsilylallyl@
  49771. tscn@
  49772. unactivated@
  49773. undergoboth@
  49774. unstable@
  49775. unusual@
  49776. successfully
  49777. amines
  49778. anilines
  49779. indoles@
  49780. using
  49781. using
  49782. catalyzed
  49783. cyclization
  49784. addition
  49785. short
  49786. synthesis
  49787. various
  49788. lewis
  49789. acids
  49790. studied@
  49791. varying@
  49792. verlag
  49793. vinyl
  49794. halides
  49795. efficiently
  49796. converted
  49797. under
  49798. vinyl/aryl
  49799. stannanes
  49800. couple
  49801. smoothly
  49802. polymer
  49803. bound
  49804. aryl@
  49805. wereisolated@
  49806. which
  49807. while@
  49808. wiley-interscience@
  49809. equivalents
  49810. reductive
  49811. cyclization
  49812. occurs
  49813. workup@
  49814. yield
  49815. yields
  49816. 23-63@
  49817. yields
  49818. better
  49819. ch2cl2
  49820. better
  49821. stereoselectivity
  49822. zincate@
  49823. zni2is@
  49824. tricyclooctanones
  49825. triene
  49826. trienes
  49827. triesters
  49828. triethylaluminum
  49829. triethylamine
  49830. triethylborohydride
  49831. triethylsilane
  49832. triethylsilane/boron
  49833. triethylsilyl
  49834. triethylsilyloxymeth
  49835. triflate
  49836. triflates
  49837. triflone
  49838. triflones
  49839. trifluoride
  49840. trifluoro
  49841. trifluoroethanimidam
  49842. trifluoroethanols
  49843. trifluoromethylation
  49844. trifluoromethylspiro
  49845. trifluoromethyltrime
  49846. triflyloxy
  49847. trifunctionalised
  49848. triggers
  49849. triisopropylsilaneth
  49850. triisopropylsilaneth
  49851. hstips
  49852. easily
  49853. prepared
  49854. yield
  49855. triisopropylsilyl
  49856. triketone
  49857. triketones
  49858. trimethyl
  49859. trimethylchlorosilan
  49860. trimethylene
  49861. trimethylsiloxy
  49862. trimethylsilyl
  49863. trimethylsilyl
  49864. glycidol
  49865. derivatives
  49866. oxidized
  49867. trimethylsilylallyl
  49868. trimethylsilylated
  49869. trimethylsilylazide
  49870. trimethylsilylmethyl
  49871. trimethylsilyloxy
  49872. trimethylsilylpropar
  49873. trimethylsilyltrifla
  49874. triorgano
  49875. triorganosilyl
  49876. trioxaadamantane
  49877. triphenylphosphine
  49878. triphosgene
  49879. triple
  49880. triplet
  49881. trimethylsilyl
  49882. silane
  49883. relatively
  49884. alternative
  49885. trisubstituted
  49886. tropane
  49887. tropanes
  49888. tropinone
  49889. trost
  49890. trost
  49891. angew
  49892. 199231
  49893. trost
  49894. tryptophan
  49895. turned
  49896. bonds
  49897. readily
  49898. formed
  49899. nucleophilic
  49900. addition
  49901. effective
  49902. synthetic
  49903. approaches
  49904. euryfuran
  49905. descri
  49906. types
  49907. typical
  49908. tyrosine
  49909. brinker
  49910. press
  49911. greenwich
  49912. ullmann
  49913. ulose
  49914. ultimately
  49915. ultrasound
  49916. ultraviolet
  49917. unaffected
  49918. uncatalyzed
  49919. unchanged
  49920. uncommon
  49921. undecane
  49922. undecanones
  49923. under
  49924. under
  49925. conditions
  49926. kinetic
  49927. control
  49928. diastereoselecti
  49929. under
  49930. palladium
  49931. catalysis
  49932. various
  49933. allylester
  49934. protecting
  49935. under
  49936. these
  49937. conditions
  49938. reaction
  49939. instant
  49940. undergo
  49941. undergoboth
  49942. undergoes
  49943. undergoing
  49944. understood
  49945. underwent
  49946. undesired
  49947. unequivocally
  49948. unexpected
  49949. unformed
  49950. unhindered
  49951. unimolecuiar
  49952. units
  49953. universit
  49954. university
  49955. university
  49956. science
  49957. books
  49958. univesity
  49959. univesity
  49960. science
  49961. books
  49962. unlike
  49963. unlike
  49964. other
  49965. azides
  49966. bearing
  49967. electron
  49968. withdrawing
  49969. ortho
  49970. unnatural
  49971. unprecedented
  49972. unreacted
  49973. unreactive
  49974. unsaturated
  49975. unsaturated
  49976. esters
  49977. formed
  49978. cyclopropanone
  49979. acetals
  49980. unsaturation
  49981. unselective
  49982. unsuccessful
  49983. unsymmetrical
  49984. unsymmetrical
  49985. tetrasulfides
  49986. prepared
  49987. unsymmetrically
  49988. unusual
  49989. unwanted
  49990. ureas
  49991. ureidomercuration
  49992. amines
  49993. anilines
  49994. indoles
  49995. remove
  49996. allyl
  49997. presence
  49998. useful
  49999. usefulnes
  50000. usefulness
  50001. using
  50002. using
  50003. catalyzed
  50004. cyclization
  50005. addition
  50006. short
  50007. synthesis
  50008. using
  50009. sncl4
  50010. yield
  50011. syn/anti
  50012. ticl2
  50013. using
  50014. supercritical
  50015. solvent
  50016. higher
  50017. usual
  50018. usually
  50019. utility
  50020. utilized
  50021. utilizing
  50022. publishers
  50023. vacuum
  50024. value
  50025. values
  50026. nostrand
  50027. reinhold
  50028. vaporization
  50029. variable
  50030. variation
  50031. variations
  50032. varied
  50033. variety
  50034. various
  50035. various
  50036. amino
  50037. acids
  50038. employed
  50039. 37-65
  50040. yields
  50041. 74-88
  50042. various
  50043. lewis
  50044. acids
  50045. studied
  50046. various
  50047. nucleophiles
  50048. coome
  50049. naoph
  50050. nasph
  50051. publishers
  50052. verlagsgesellschaft
  50053. verla
  50054. verlag
  50055. verlag
  50056. verlag
  50057. verlag
  50058. verlag
  50059. helvetica
  50060. chimica
  50061. verlagsgesellschaft
  50062. versatile
  50063. version
  50064. versus
  50065. viability
  50066. vicinal
  50067. vicinally
  50068. vigabatrin
  50069. vigorously
  50070. villiger
  50071. vilsmeier
  50072. vinblastine
  50073. vineomycins
  50074. vinyl
  50075. efficiently
  50076. converted
  50077. under
  50078. vinyl
  50079. group
  50080. vinyl
  50081. alkylate
  50082. vinyl
  50083. benzoate
  50084. vinyl/aryl
  50085. vinyl/aryl
  50086. stannanes
  50087. couple
  50088. smoothly
  50089. polymer
  50090. bound
  50091. vinylamine
  50092. vinylamines
  50093. vinylation
  50094. vinylazido
  50095. vinylaziridine
  50096. vinylbut
  50097. vinylcyclopropanes
  50098. vinylic
  50099. vinylidene
  50100. vinylol
  50101. vinylpalladium
  50102. vinylsilanes
  50103. vinylstannanes
  50104. nylthionium
  50105. virtue
  50106. visible
  50107. voacanga
  50108. 17181994
  50109. yield
  50110. wulff
  50111. comprehensive
  50112. organic
  50113. synthesis
  50114. trost
  50115. fleming
  50116. wadsworth
  50117. walden
  50118. warming
  50119. warsz
  50120. wasaccomplished
  50121. wasexamined
  50122. washington
  50123. wasinvestigated
  50124. wasseparated
  50125. watanabe
  50126. water
  50127. synthesis
  50128. peripla
  50129. report
  50130. preparation
  50131. hydroisoquinoline
  50132. intermediat
  50133. weakens
  50134. weakly
  50135. weinreb
  50136. cyano
  50137. selena
  50138. dihydro
  50139. ethanoan
  50140. 2-chloropyridne
  50141. adduct
  50142. neared
  50143. reagent
  50144. prepared
  50145. equimolar
  50146. quantitie
  50147. and/or
  50148. phch2ch2
  50149. formed
  50150. where
  50151. whereas
  50152. whereby
  50153. whether
  50154. which
  50155. which
  50156. whilst
  50157. whisky
  50158. wiley
  50159. wiley
  50160. chichester
  50161. wiley-interscience
  50162. wilkinson's
  50163. priate
  50164. withdrawing
  50165. within
  50166. without
  50167. wittig
  50168. wolfe
  50169. wolfe
  50170. medical
  50171. wolff
  50172. workers
  50173. works
  50174. would
  50175. wulff
  50176. wydawn
  50177. wydawn
  50178. politech
  50179. warsz
  50180. co2me
  50181. x-ray
  50182. xanthate
  50183. xylofuranoses
  50184. xylose
  50185. tetrahedron
  50186. asymmetry
  50187. yamamoto
  50188. years
  50189. yield
  50190. yield
  50191. yield
  50192. after
  50193. oxidation
  50194. quinone
  50195. yielded
  50196. yielding
  50197. yields
  50198. ratio
  50199. greater
  50200. 62-88
  50201. yields
  50202. yields
  50203. yields
  50204. better
  50205. ch2cl2
  50206. better
  50207. stereoselectivity
  50208. yields
  50209. generally
  50210. better
  50211. yields
  50212. nearly
  50213. quantitative
  50214. cases
  50215. yields
  50216. generally
  50217. yields
  50218. generally
  50219. yields
  50220. generally
  50221. better
  50222. yields
  50223. generally
  50224. better
  50225. giving
  50226. yields
  50227. range
  50228. between
  50229. yields
  50230. amines
  50231. including
  50232. diisopro
  50233. ylide
  50234. ylidene
  50235. ylides
  50236. yohimbine
  50237. trimethylsilyl
  50238. diyne
  50239. prepared
  50240. z-chloroallylphospho
  50241. z-enolate
  50242. z-titanium
  50243. z-vinyl
  50244. z/cis
  50245. z/trans
  50246. zeolites
  50247. zimmerman-traxler
  50248. zn/ag
  50249. znbr2
  50250. zncl2
  50251. zni2is
  50252. zwitterion
  50253. zwitterionic
  50254. paleta
  50255. ionic
  50256. addition
  50257. reactions
  50258. halomethanes
  50259. fluor@
  50260. 13-asymmetric
  50261. induction
  50262. aldol
  50263. addition
  50264. reactions
  50265. triphenylphosphorany
  50266. propane
  50267. novel
  50268. chch2n
  50269. 1-alkoxy-1-siloxycyc
  50270. homoenolate
  50271. nucleophiles
  50272. esters@
  50273. wittig
  50274. rearrangement
  50275. alkoxy
  50276. alkyllithiums
  50277. inversion
  50278. 12-diazocines
  50279. 13-diazocines
  50280. triazocines
  50281. tetrazocines@
  50282. addition
  50283. reactions
  50284. halomethanes
  50285. fluor
  50286. 0ligopyridines
  50287. 0rganic
  50288. 0rganomet
  50289. 0xabicyclo
  50290. 0xadiazin
  50291. 0xathiacycloalkanes
  50292. 0xazaphosphorinane
  50293. 0xazin
  50294. 0xazine
  50295. 0xazines
  50296. 0xazoles
  50297. 0xides
  50298. 0xidopyridmium
  50299. 0xidopyrylium
  50300. 0xoalkanenitriles
  50301. aldol
  50302. addition
  50303. reactions
  50304. butadienyl
  50305. pyridinium
  50306. bromide
  50307. novel
  50308. diene
  50309. diels
  50310. homocubene
  50311. homocubylidene
  50312. theoretical
  50313. investigatio
  50314. novel
  50315. easily
  50316. accessible
  50317. chiral
  50318. ferrocenyldiphosphin
  50319. absolute
  50320. stereochemistry
  50321. aplyronine
  50322. potent
  50323. antitumo
  50324. arylamino
  50325. dihydro
  50326. imidazole
  50327. thiones
  50328. react
  50329. triphenylphosphorany
  50330. propane
  50331. novel
  50332. chch2n
  50333. triphenylphosphorany
  50334. propane
  50335. novel
  50336. chch2n
  50337. benzenesulfonyl
  50338. trimethylsilylacetyl
  50339. acetylene
  50340. benzenesulfonyl
  50341. trimethylsilyl
  50342. acetylene
  50343. acetylen
  50344. catalytic
  50345. asymmetric
  50346. hydrogenation
  50347. imines
  50348. chiral
  50349. diastereo
  50350. enantioselective
  50351. synthesis
  50352. allenylcarbino
  50353. extension
  50354. colvin
  50355. rearrangement
  50356. using
  50357. trimethylsilyl
  50358. phosphirenes
  50359. synthesis
  50360. preparative
  50361. significanc
  50362. lithium
  50363. dialkylamide
  50364. mixed
  50365. aggregation
  50366. comutational
  50367. rapid
  50368. construction
  50369. roflamycoin
  50370. system
  50371. 1'-methylbenzyl
  50372. 1-arylquinolinium
  50373. salts
  50374. 1-acyl-2
  50375. 1-acyl-4-methoxypyri
  50376. 1-alkenyl
  50377. 1-alkenyl
  50378. anions
  50379. vinyl
  50380. carbanions
  50381. 1-alkenyl
  50382. phosphorus
  50383. compounds
  50384. 1-alkenylidene
  50385. 1-alkenylidene
  50386. 12-alkadienylidene
  50387. other
  50388. related
  50389. ketenes
  50390. 1-alkoxy-1-diazoalka
  50391. 1-alkoxy-1-siloxycyc
  50392. 1-alkoxy-1-siloxycyc
  50393. homoenolate
  50394. nucleophiles
  50395. esters
  50396. 1-alkyl
  50397. 1-alkynes
  50398. 1-alkynyl
  50399. 1-alkynyl
  50400. anions
  50401. 1-alkynylcyclobuteno
  50402. 1-amino-3
  50403. 1-aryl-substituted
  50404. 1-arylnaphthalene
  50405. 1-arylquinolinium
  50406. 1-azaspiro
  50407. 1-azido-12-benziodox
  50408. 1-azido-33-bis
  50409. 1-benzofurans
  50410. 1-benzofurans
  50411. benzo
  50412. furans
  50413. 1-benzopyrylium
  50414. 1-benzopyrylium
  50415. salts
  50416. 1-benzothiophenes
  50417. 1-benzothiopyrylium
  50418. 1-benzothiopyrylium
  50419. salts
  50420. 1-benzoyl-2-alkyl-3
  50421. porphyrins
  50422. 1-cyclopropylideneal
  50423. 1-deoxylycorine
  50424. 1-diazo-1-alkenes
  50425. 1-diazo-1-haloalkane
  50426. 1-donor
  50427. 1-halo
  50428. 1-halo
  50429. 12-dihalocyclopropen
  50430. chemical
  50431. synthesis
  50432. 1-halo-1h-phosphiren
  50433. 1-halo-1h-phosphiren
  50434. synthesis
  50435. preparative
  50436. significance
  50437. 1-haloalkyl
  50438. 1-hetero-1-metalloxy
  50439. 1-hydroxy
  50440. 1-hydroxyalkyl
  50441. 1-hydroxyindoles
  50442. 1-hydroxypyrroles
  50443. 1-hydroxypyrroles
  50444. 1-hydroxyindoles
  50445. 9-hydroxycarbazoles
  50446. 1-metallo-1-seleno-c
  50447. 1-metallo-1-silyl-cy
  50448. 1-methylindol-2-yl
  50449. -alkynes
  50450. 1-o-acetyl
  50451. 1-oxa
  50452. 1-oxide
  50453. 1-oxides
  50454. 1-oxy-1-alkynes
  50455. 1-p-1-alkynes
  50456. 1-pyrrolines
  50457. 1-substituted-1234-t
  50458. 1-triisopropylsilylg
  50459. 1-vinyl
  50460. 1.1.1
  50461. 10/11
  50462. years
  50463. biginelli
  50464. dihydropyridine
  50465. synthesis
  50466. 10117q
  50467. 10147
  50468. 10175
  50469. 10199
  50470. 104-2
  50471. 10441
  50472. 10443
  50473. 10611p
  50474. 10749
  50475. tetra
  50476. butyl
  50477. butadiene
  50478. dimethyl
  50479. silirene
  50480. 11'-binaphthalene-22
  50481. 11'-binaphthalene-22
  50482. chiral
  50483. auxiliary
  50484. diastereoselectiv
  50485. 11-dichloroalkyl
  50486. 11-difluoroallene
  50487. 11-dihaloalkenes
  50488. 11-dihaloalkyl
  50489. 11-dihaloalkyl
  50490. heterocumulenes
  50491. synthesis
  50492. reactions
  50493. 11-dihalocyclopropan
  50494. atile
  50495. ligand
  50496. 11065
  50497. 11115
  50498. 111333
  50499. 111520
  50500. 112934
  50501. 15-stereocontrols
  50502. 5-hexenyl
  50503. radical
  50504. cyclizations
  50505. asymmetric
  50506. induction
  50507. allylation
  50508. organocoppe
  50509. azoxy
  50510. rearrangement
  50511. fragmentation
  50512. azoxy
  50513. radicals
  50514. arylsulfonyl
  50515. alkenes
  50516. review
  50517. dibromoalk
  50518. enylidenes
  50519. opening
  50520. dibromo
  50521. dibromoethane
  50522. synthesis
  50523. bromoesters
  50524. brominati
  50525. dioxetane
  50526. synthesis
  50527. characterization
  50528. stability
  50529. chemil
  50530. wittig
  50531. rearrangement
  50532. alkoxy
  50533. alkyllithiums
  50534. inversion
  50535. wittig
  50536. rearrangement
  50537. enantio
  50538. defined
  50539. alkoxyalkyllith
  50540. 12-addition
  50541. 12-addition
  50542. alkyl
  50543. alkenylzirconocene
  50544. chlorides
  50545. 12-additions
  50546. 12-additions
  50547. heteroatom-substitut
  50548. olefins
  50549. organopallad
  50550. 12-alkadienylidene
  50551. 12-anionic
  50552. 12-anionic
  50553. rearrangements
  50554. organosilicon
  50555. germanium
  50556. 12-asymmetric
  50557. 12-asymmetric
  50558. induction
  50559. reactions
  50560. nonconjugated
  50561. acycli
  50562. 12-asymmetric
  50563. induction
  50564. insertion
  50565. reaction
  50566. 12-benzenediolato
  50567. 12-benziodoxol
  50568. 12-benzothiazoles
  50569. 12-benzoxazoles
  50570. 12-bis
  50571. 12-bis
  50572. arylsulfonyl
  50573. alkenes
  50574. 12-carbonyl
  50575. 12-catalyzed
  50576. 12-chiral
  50577. 12-cyclic
  50578. 12-di-n-1-alkenes
  50579. 12-di-p-1-alkenes
  50580. 12-dialkylidenecyclo
  50581. 12-diazete
  50582. 12-diazetidines
  50583. 12-diazetidines
  50584. dihydro-12-diazetes
  50585. 12-diazete
  50586. 12-diazine
  50587. 12-diazocines
  50588. 12-diazocines
  50589. 13-diazocines
  50590. triazocines
  50591. tetrazocines
  50592. 12-dicyano-12-dithio
  50593. 12-dihalocyclopropen
  50594. 12-diols
  50595. 12-dioxides
  50596. 12-dioxy-substituted
  50597. 12-disubstituted
  50598. 12-dithiins
  50599. 12-dithiolanes
  50600. 12-dithioles
  50601. 12-dithiolium
  50602. 12-dithiolium
  50603. salts
  50604. related
  50605. compounds
  50606. 12-elimination
  50607. 12-eliminations
  50608. 12-epoxides
  50609. 12-metallate
  50610. 12-oxazetidines
  50611. 12-oxazetidines
  50612. 4h-12-oxazetes
  50613. 12-oxazoles
  50614. 12-oxazoles
  50615. isoxazoles
  50616. 12-prototropy
  50617. 12-silicon
  50618. 12-thiazoles
  50619. 12-trans-ribofuranos
  50620. 12-vinyl
  50621. 12-ylides
  50622. 12111222
  50623. 12159
  50624. 124-oxadiazoles
  50625. 123-benzodithiazoium
  50626. 123-benzodithiazoium
  50627. salts
  50628. 123-benzothiadiazole
  50629. 123-dioxazetidines
  50630. 123-dioxazetidines
  50631. 123-oxathiazetidines
  50632. 123-oxadiazetidines
  50633. 123-dithiazolium
  50634. 123-dithiazolium
  50635. salts
  50636. 123-oxadiazetidines
  50637. 123-oxadiazoles
  50638. 123-oxathiazetidines
  50639. 123-thiadiazoles
  50640. 123-thiadiazoles
  50641. 123-benzothiadiazole
  50642. including
  50643. their
  50644. 123-thiadiazoles
  50645. benzo
  50646. derivatives
  50647. 123-tri
  50648. 123-tri
  50649. zines
  50650. their
  50651. benzo
  50652. derivatives
  50653. 123-triaza
  50654. 123-triazetidines
  50655. 123-triazoles
  50656. 123-triazoles
  50657. their
  50658. benzo
  50659. derivatives
  50660. 123-triazolium-1-yli
  50661. 123-trithianes
  50662. 1234-oxatriazoles
  50663. 1235@
  50664. 1251@
  50665. dipolar
  50666. cycloaddition
  50667. approach
  50668. towards
  50669. stereoselectiv@
  50670. 13-diazetidines
  50671. dihydro-13-diazetes
  50672. 13-diazetes@
  50673. 13-dipolar
  50674. cycloaddition
  50675. chemistry@
  50676. 135-triazines
  50677. 14-carbosilylation@
  50678. method
  50679. obtaining
  50680. unusual
  50681. 1511@
  50682. 16167@
  50683. 18-di@
  50684. 197912
  50685. 198014
  50686. 198119123@
  50687. 198218@
  50688. 198316
  50689. 1990156
  50690. 19929
  50691. 1994~
  50692. cycloadditions@
  50693. ylenetet
  50694. 124-dithiazolium
  50695. 124-dithiazolium
  50696. salts
  50697. 124-oxadiazoles
  50698. 124-thiadiazoles
  50699. 124-thiadiazoles
  50700. including
  50701. 124-thiadiazolium
  50702. salts
  50703. 124-thiadiazolium
  50704. 124-triazines
  50705. 124-triazines
  50706. their
  50707. benzo
  50708. derivatives
  50709. 124-triazol
  50710. 124-triazoles
  50711. 124-triazolines
  50712. 124-triazolo
  50713. 124-triazolo
  50714. pyrimidin
  50715. 1245-tetrathianes
  50716. 1245-tetrathianes
  50717. syntheses
  50718. reactions
  50719. 1245-tetrathianes
  50720. structure
  50721. spectroscopic
  50722. properties
  50723. 1246-thiatriazines
  50724. 125-dihydroxyvitamin
  50725. 125-oxadiazoles
  50726. 125-oxadiazoles
  50727. their
  50728. benzo
  50729. derivatives
  50730. 125-thiadiazoles
  50731. 125-thiadiazoles
  50732. their
  50733. benzo
  50734. derivatives
  50735. 12521o
  50736. 12:23-bis-epoxide
  50737. 12shifts
  50738. butadiynyl
  50739. hydrazines
  50740. class
  50741. electron
  50742. alkadi
  50743. dipolar
  50744. addition
  50745. oximes
  50746. olefins
  50747. dipolar
  50748. cycloaddition
  50749. approach
  50750. towards
  50751. stereoselectiv
  50752. dipolar
  50753. cycloaddition
  50754. diazoalkanes
  50755. nitrogen
  50756. dipolar
  50757. cycloaddition
  50758. fragment
  50759. aromatic
  50760. dipolar
  50761. cycloadditions
  50762. diazo
  50763. alkanonones
  50764. nitro
  50765. dipolar
  50766. cycloadditions
  50767. ethoxycarbonyl
  50768. nitrile
  50769. benzylim
  50770. dipolar
  50771. cycloreversions
  50772. elimination
  50773. reactionos
  50774. epoxy
  50775. butyl
  50776. stannanes
  50777. approa
  50778. oxazine
  50779. derivatives
  50780. 13-alkadienes
  50781. 13-alkadienes
  50782. their
  50783. derivatives
  50784. reactions
  50785. electr
  50786. 13-alkenynes
  50787. 13-allylic
  50788. 13-amine
  50789. 13-anionic
  50790. 13-anionic
  50791. cycloadditions
  50792. organolithium
  50793. compounds
  50794. 13-asymmetric
  50795. 13-benzothiazoles
  50796. 13-benzoxazoles
  50797. 13-butadienes
  50798. 13-cyclohexadiene
  50799. 13-cyclohexadiene
  50800. formation
  50801. reactions
  50802. 13-diastereoselectiv
  50803. 13-diastereoselectiv
  50804. o-displacement
  50805. enolates
  50806. 13-diazetes
  50807. 13-diazetidines
  50808. 13-diazetidines
  50809. dihydro-13-diazetes
  50810. 13-diazetes
  50811. 13-diazocines
  50812. 13-diene
  50813. 13-dienes
  50814. 13-difunctionality
  50815. 13-dihydroindol-2-on
  50816. 13-diolD
  50817. 13-dioxide
  50818. 13-dioximes
  50819. 13-dioxolium
  50820. 13-dioxolium
  50821. salts
  50822. 13-dipolar
  50823. polar
  50824. cycloaddition
  50825. chemistry
  50826. 13-dipolar
  50827. cycloadditions
  50828. diazoalkanes
  50829. nitrogen
  50830. 13-dipolar
  50831. cycloreversions
  50832. 13-dipoles
  50833. 13-dithiane
  50834. 13-dithioles
  50835. 13-dithiolium
  50836. 13-dithiolium
  50837. salts
  50838. 13-oxathiolium
  50839. 13-oxathiolium
  50840. salts
  50841. 13-oxazetidines
  50842. 13-oxazetidines
  50843. 4h-13-oxazetes
  50844. 13-oxazines
  50845. 13-oxazines
  50846. 13-thiazines
  50847. intermediates
  50848. interest
  50849. 13-oxazoles
  50850. 13-polyols
  50851. 13-strain
  50852. 13-thiazines
  50853. 13-thiazoles
  50854. 13049n
  50855. 13193
  50856. 132-benzodithiazoliu
  50857. 132-benzodithiazoliu
  50858. salts
  50859. 132-dithiazolium
  50860. 132-dithiazolium
  50861. salts
  50862. 132-oxazaphosphole
  50863. 13246
  50864. 133-trichloro-2-aza
  50865. 13315m
  50866. 134-oxadiazoles
  50867. 134-thiadiazoles
  50868. 134-thiadiazoles
  50869. 134-thiadiazolium
  50870. compounds
  50871. 134-thiadiazolium
  50872. 135-triazines
  50873. 135-triazines
  50874. 135-trioxanes
  50875. 135-tris
  50876. 135-tris
  50877. dialkylamino
  50878. benzenes
  50879. model
  50880. compounds
  50881. elect
  50882. 13alkadienes
  50883. lattice
  50884. relaxation
  50885. times
  50886. mobility
  50887. organi
  50888. addition
  50889. reactions
  50890. organocuprates
  50891. unsaturated
  50892. dihydropyridines
  50893. effects
  50894. chirality
  50895. conformation
  50896. 14-addition
  50897. 14-addition
  50898. secondary
  50899. tertiary
  50900. alkylzinc
  50901. bromides
  50902. 14-addition
  50903. reactions
  50904. organocuprates
  50905. alpha
  50906. beta-unsa
  50907. 14-additions
  50908. 14-addtion
  50909. 14-benzodiazepines
  50910. 14-benzothiazines
  50911. 14-biradicals
  50912. carbonyl
  50913. 14-dienes
  50914. 14-dihalo-1-alkene
  50915. 14-dihydroazetes
  50916. 14-dihydrobe
  50917. 14-dihydronaphthalen
  50918. 14-dihydropyridines
  50919. 14-dihydropyridines
  50920. effect
  50921. chirality
  50922. conformation
  50923. 14-dioxene
  50924. 14-membered
  50925. 142-dithiazoliu
  50926. 142-dithiazoliu
  50927. salts
  50928. 145770
  50929. 14753
  50930. 14:36
  50931. 14:36-dianhydrohexit
  50932. 14dioxin
  50933. biradicals
  50934. membered
  50935. rings
  50936. generated
  50937. delta
  50938. dipolar
  50939. cyclizations
  50940. method
  50941. obtaining
  50942. unusual
  50943. electrocyclization
  50944. azomethine
  50945. ylides
  50946. their
  50947. applica
  50948. electrocyclization
  50949. vinyl
  50950. dipoles
  50951. methods
  50952. michael
  50953. addition
  50954. intramolecular
  50955. homolytic
  50956. aromatic
  50957. substitution
  50958. years
  50959. reductive
  50960. coupling
  50961. learned
  50962. 15-addition
  50963. 15-addition
  50964. halogens
  50965. pseudohalogens
  50966. cyclopropylthi
  50967. 15-benzodiazepines
  50968. 15-biradicals
  50969. 15-biradicals
  50970. five-membered
  50971. rings
  50972. generated
  50973. delta-hyd
  50974. 15-cyclooctadiene
  50975. 15-cyclooctadiene
  50976. bis-homodiene
  50977. partner
  50978. metal-cata
  50979. 15-dehydronaphthalen
  50980. 15-diazocines
  50981. 15-dipolar
  50982. 15-dipolar
  50983. cyclisations
  50984. 15-dipoles
  50985. 15-diynes
  50986. 15-enynes
  50987. 15-stereocontrols
  50988. 15/16
  50989. 15139
  50990. 15154
  50991. 153ff3
  50992. dehydro
  50993. 16-diynes
  50994. 16-electron
  50995. 16111
  50996. 16122
  50997. 16126
  50998. 16131
  50999. 16167
  51000. 17-asymmetric
  51001. 17-dienes
  51002. 17-electrocyclic
  51003. 17-electrocyclic
  51004. reactions
  51005. alpha
  51006. gamma
  51007. delta
  51008. unsatur
  51009. 17-enynes
  51010. spectroscopy
  51011. assessment
  51012. steric
  51013. perturbation
  51014. 18-bis
  51015. 18129
  51016. 19-disubstituted
  51017. 19-disubstituted
  51018. triptycenes
  51019. excellent
  51020. probe
  51021. 19-electron
  51022. 19-electron
  51023. organometallic
  51024. adducts
  51025. 1975.1978
  51026. 1977-1988
  51027. 197710
  51028. 197710175
  51029. 1977145
  51030. 1977155
  51031. 197716
  51032. 19781
  51033. 197811
  51034. 197811107
  51035. 197811141
  51036. 197812
  51037. 197814
  51038. 197816
  51039. 1978161
  51040. 1978165
  51041. 197817
  51042. 1978171
  51043. 1978193
  51044. 1979-1985
  51045. 197911
  51046. 197912
  51047. 197912
  51048. 197912125
  51049. 197912132
  51050. 19791214
  51051. 197912146
  51052. 197912191
  51053. 197912198
  51054. 197913
  51055. 197918
  51056. 1979181
  51057. 19801
  51058. 198012
  51059. 1980121
  51060. 19801213
  51061. 198013
  51062. 1980131
  51063. 198013113
  51064. 198013161
  51065. 198014
  51066. 198014
  51067. 1980141825
  51068. 1980165
  51069. 198018
  51070. 198019
  51071. 1981-1989
  51072. 19811
  51073. 198110
  51074. 1981100
  51075. 1981100129
  51076. 198112
  51077. 198112119
  51078. 198113
  51079. 198114
  51080. 198115
  51081. 1981151323
  51082. 1981151349
  51083. 1981151395
  51084. 198116
  51085. 1981161009
  51086. 1981161243
  51087. 1981161587
  51088. 1981161755
  51089. 1981165
  51090. 198117
  51091. 1981171
  51092. 198118
  51093. 1981181485
  51094. 1981185
  51095. 198119
  51096. 198119123
  51097. 19821
  51098. 1982101
  51099. 1982101193
  51100. 1982102
  51101. 1982102111
  51102. 1982102147
  51103. 1982104
  51104. 1982105
  51105. 1982106
  51106. 198211
  51107. 19821115
  51108. 198211191
  51109. 198213
  51110. 198213117
  51111. 198213195
  51112. 198214
  51113. 198215
  51114. 198215117
  51115. 198215128
  51116. 19821513
  51117. 198215164
  51118. 198217
  51119. 198218
  51120. 1982181
  51121. 198218187
  51122. 198219
  51123. 198219111
  51124. 1982191148
  51125. 1982191295
  51126. 1982191685
  51127. 1982191735
  51128. 1983112
  51129. 1983113
  51130. 1983115
  51131. 198312
  51132. 198312129
  51133. 198314
  51134. 198314115
  51135. 198314165
  51136. 198314183
  51137. 198315
  51138. 198316
  51139. 198316
  51140. 1983161
  51141. 198316161
  51142. 198316177
  51143. 1983169
  51144. 198319
  51145. 1983191
  51146. 198319131
  51147. 19841031
  51148. 1984116
  51149. 1984121
  51150. 198412i
  51151. 198413
  51152. 198415
  51153. 198416199
  51154. 198417
  51155. 198417109
  51156. 198417180
  51157. 1985-present
  51158. 1987s92
  51159. 19881
  51160. 1988107
  51161. 198812
  51162. 198814177
  51163. 1988144
  51164. 1988146
  51165. 1988149
  51166. 198817
  51167. 198818
  51168. 198818129
  51169. 1989108
  51170. 198913
  51171. 1989150
  51172. 198918
  51173. 198919
  51174. 1989191
  51175. 19901
  51176. 1990109
  51177. 199013
  51178. 199014
  51179. 1990153
  51180. 1990154
  51181. 1990155
  51182. 1990156
  51183. 1990156
  51184. 199017
  51185. 1990171
  51186. 199017159
  51187. 199019
  51188. 199023
  51189. 199050158
  51190. 199062
  51191. 1990s
  51192. 199110
  51193. 199111
  51194. 1991110
  51195. 1991121
  51196. 199115
  51197. 199116
  51198. 199140407
  51199. 19914527
  51200. 199160
  51201. 19918
  51202. lemieux
  51203. award
  51204. lecture
  51205. studies
  51206. related
  51207. penicillin
  51208. 1992111
  51209. 199212
  51210. 199216
  51211. 1992163
  51212. 199221
  51213. 199225
  51214. 1992411
  51215. 199246
  51216. 1992591
  51217. 199259141
  51218. 199261
  51219. 199264
  51220. 19929
  51221. 19929
  51222. lemieux
  51223. award
  51224. lecture
  51225. organometallic
  51226. reactions
  51227. 199310
  51228. 1993112
  51229. 199313
  51230. 199314149
  51231. 1993164
  51232. 1993165
  51233. 1993166
  51234. 1993167
  51235. 1993168
  51236. 199317
  51237. 199318
  51238. 199319
  51239. 1993191
  51240. 199319183
  51241. 199322
  51242. 1993259
  51243. 199326
  51244. 199332
  51245. 199349
  51246. 199358123
  51247. 199362
  51248. 199393
  51249. 1994J
  51250. 1994~
  51251. 19941
  51252. 199411
  51253. 1994113
  51254. 1994169
  51255. 199418
  51256. 199430
  51257. 199433
  51258. 199450
  51259. 199463
  51260. 199466
  51261. 199494
  51262. 1abeled
  51263. azepine
  51264. spectroscopic
  51265. chemical
  51266. characterization
  51267. 2h-isoindoles
  51268. 1h-imidazoles
  51269. 1h-pyrazoles
  51270. 2-methylene-13-dithi
  51271. 13-dioxide
  51272. highly
  51273. reactive
  51274. 1s-2-x-alkenes
  51275. fischer
  51276. carbene
  51277. complexe
  51278. cycloaddition
  51279. seleno-2-silylethene
  51280. selenium
  51281. assisted
  51282. cycloadditions
  51283. cyloaddition
  51284. cycloreversion
  51285. reactions
  51286. heteroc
  51287. photocycloaddition/f
  51288. strategies
  51289. synthesis
  51290. azafulvenium
  51291. vinyl
  51292. pyrrole
  51293. complex
  51294. osmium
  51295. ethoxybut
  51296. dimethylhydrazone
  51297. useful
  51298. reagent
  51299. heteroatom-substitut
  51300. methyl
  51301. penems
  51302. nitrogen
  51303. deriv
  51304. heteroatom-substitut
  51305. methyl
  51306. penems
  51307. oxygen
  51308. derivatives
  51309. isopropylapoisopinoc
  51310. improved
  51311. reagent
  51312. asymmetri
  51313. monosubstituted
  51314. oxazolidines
  51315. improved
  51316. protective
  51317. styrylchromones
  51318. biological
  51319. action
  51320. synthesis
  51321. reactivity
  51322. 2-alkenoic
  51323. 2-alkenyl
  51324. 2-alkenyloxazolidine
  51325. 2-alkyl
  51326. 2-alkyl-13-cyclopent
  51327. 2-alkyltetrahydropyr
  51328. 2-alkynlaniline
  51329. 2-alkynyl
  51330. 2-amino-13-dienes
  51331. 2-amino-2-deoxy
  51332. 2-aminobenzimidazole
  51333. 2-aminobenzimidazole
  51334. organic
  51335. synthes
  51336. 2-aminobenzophenones
  51337. 2-aminooxy-1-s-alken
  51338. 2-aminosaccharides
  51339. 2-aryl-4methylenetet
  51340. 2-aryl-boc-pyrrolidi
  51341. 2-arylpropionic
  51342. 2-aza-13-dienes
  51343. 2-azaallyl
  51344. 2-benzofurans
  51345. 2-benzopyrylium
  51346. 2-benzopyrylium
  51347. salts
  51348. 2-benzothiophenes
  51349. 2-benzothiophenes
  51350. benzo
  51351. thiophenes
  51352. 2-benzoylamino-3-dim
  51353. 2-butenanildes
  51354. 2-butene-14-diyl
  51355. 2-butenylstannanes
  51356. 2-carbalkoxycycloalk
  51357. 2-carboxaldehyde
  51358. 2-carboxylic
  51359. 2-cycloalkenones
  51360. 2-cyclohexenones
  51361. 2-cyclopenten-1-ones
  51362. 2-cyclopentenone
  51363. 2-desoxystemodine
  51364. 2-dialkylamino-14-na
  51365. 2-enone
  51366. 2-ethoxy-2-propenyli
  51367. 2-exo-hydroxy-10-bor
  51368. 2-fluoroalkyl
  51369. 2-fluoroalkyl
  51370. a-ring
  51371. analogs
  51372. 125-dihydroxyvitamin
  51373. 2-fold
  51374. 2-haloalkene
  51375. 2-hydrazonoazetidine
  51376. 2-hydroxy-1-hetero-1
  51377. 2-hydroxyalkanoic
  51378. 2-iminiono
  51379. 2-imino
  51380. 2-imino
  51381. 2-iminiono
  51382. 2-hydrazonoazetidine
  51383. 2-isoxazolines
  51384. 2-lithio-n-methylpip
  51385. 2-aryl-4methylenetet@
  51386. 2-azetidinones@
  51387. 2-lithio-n-methylpip
  51388. 2-lithio-n-methylpyr
  51389. configurationa@
  51390. 2-phenylsulfonyl@
  51391. 2035@
  51392. 22-dihalovinylcyclop@
  51393. 2273@
  51394. 23-dihydroindens@
  51395. cycloadditions
  51396. azides
  51397. allylic
  51398. carbocatio@
  51399. 3-amino-2h-azirine@
  51400. 3-ylidene@
  51401. 4-iminodihydroazetes@
  51402. acetyl
  51403. methyl
  51404. nitro
  51405. phenyl
  51406. pyridazinone
  51407. versati
  51408. 6-endo-dig
  51409. 2-lithio-n-methylpip
  51410. 2-lithio-n-methylpyr
  51411. configurationa
  51412. 2-lithio-n-methylpyr
  51413. 2-lithiodienes
  51414. 2-methoxycyclohexano
  51415. 2-methoxyphenyl
  51416. 2-methyl-13-propaned
  51417. 2-methyl-3
  51418. 2-methylene-13-dithi
  51419. 2-norbornyl
  51420. 2-organylapiosopinoc
  51421. 2-organylapoisopinoc
  51422. 2-organylapopinenes
  51423. 2-oxazolines
  51424. 2-oxides
  51425. 2-oxo
  51426. 2-oxo-13-oxazetidine
  51427. 2-oxoazaridines
  51428. 2-oxoazaridines
  51429. their
  51430. derivatives
  51431. 2-oxoazetidines
  51432. 2-oxoazetidines
  51433. lactams
  51434. 2-pyrones
  51435. 2-styrylchromones
  51436. 2-styrylchromones
  51437. biological
  51438. action
  51439. synthesis
  51440. reactivity
  51441. 2-substituted
  51442. 2.1.0
  51443. 2.1.0.0
  51444. 2.1.0.025
  51445. 2.1.1
  51446. 2.2.1
  51447. 2.2.2
  51448. 2.2.3
  51449. 200:1
  51450. 20135
  51451. 201379
  51452. 201435
  51453. 20160
  51454. 201615
  51455. 201815
  51456. 2037ff6
  51457. 21-benzothiazoles
  51458. 21-benzoxazoles
  51459. 21111
  51460. 21113
  51461. 21117
  51462. 21119
  51463. 21120
  51464. 21152
  51465. 21176
  51466. 21243
  51467. 213-benzothia
  51468. 213-benzothiadiazole
  51469. 216-d
  51470. dimethylcyclopropyl
  51471. methylphenyl
  51472. ketone
  51473. probe
  51474. 22'-indolylindolines
  51475. 22-dihalovinylcyclop
  51476. highly
  51477. diastereoselective
  51478. three
  51479. 22129
  51480. 221571
  51481. 221591
  51482. 22165
  51483. 22171
  51484. 221821
  51485. 22191
  51486. 22195
  51487. 222-trifluoroethyl
  51488. 223ab
  51489. dihydroisoxazoles
  51490. review
  51491. disubstituted
  51492. tetrahydrofuran
  51493. synthesis
  51494. radical
  51495. wittig
  51496. sigmatropic
  51497. rearrangements
  51498. organic
  51499. synthesis
  51500. 23-bond
  51501. 23-butadien-1-ylboro
  51502. 23-diaryl-23-dihydro
  51503. 23-didehydropiperidi
  51504. 23-dideoxyfuranoses
  51505. 23-dideoxyfuranoses
  51506. convergent
  51507. theses
  51508. 3'-dideoxy
  51509. 23-dihdroxy
  51510. 23-dihydro-14-diazep
  51511. 23-dihydro-14-diazep
  51512. 23-dihydro-14-diazep
  51513. salts
  51514. 23-dihydro-14-dioxin
  51515. 23-dihydro-4-pyridon
  51516. 23-dihydro-derivativ
  51517. 23-dihydroindenes
  51518. their
  51519. derivatives
  51520. 23-epoxy
  51521. 23-epoxypropyl
  51522. 23-fused
  51523. 23-methanoamino
  51524. 23-o-isopropylideneg
  51525. 23-oxidosqualene
  51526. 23-sigmatropic
  51527. 23-sigmatropic
  51528. rearrangements
  51529. 23-stereochemistry
  51530. 23104
  51531. 2315a
  51532. 23266-tetramethyl-35
  51533. 234-furantriones
  51534. 23678
  51535. 24-dioxo-13-diazetid
  51536. 24-dioxoazetidines
  51537. 24-dioxoazetidines
  51538. their
  51539. derivatives
  51540. 24-oxadiazetidines
  51541. 246-tri-t-butylpheny
  51542. 246-triisopropylphen
  51543. 246-triisopropylphen
  51544. selenium
  51545. bromide
  51546. tippse-br
  51547. situ-g
  51548. 246-triphenylpyryliu
  51549. 246-triphenylpyryliu
  51550. tetrafluoroborate
  51551. electron-transf
  51552. disubstituted
  51553. pyrrolidines
  51554. mannitol
  51555. derived
  51556. 25-cyclohexadien-1-o
  51557. 25-dihydroxyvitamin
  51558. 25-diketopiperazines
  51559. 25-disubstituted
  51560. 25-furanocyclic
  51561. 26-di-t-butylpyridin
  51562. 26-di-t-butylpyridin
  51563. unusual
  51564. 26-di-tert-butyl-4-m
  51565. 26-diaryl
  51566. 26-diphenylphenoxide
  51567. 26-fashion
  51568. 26122
  51569. 26135
  51570. 27-octadienyl
  51571. 27183
  51572. 28127
  51573. 28183
  51574. 29142
  51575. 29151
  51576. 291972
  51577. 2h-isoindoles
  51578. cyclophanes
  51579. paracyclophanes
  51580. superphane
  51581. cycloadditions
  51582. azides
  51583. allylic
  51584. carbocatio
  51585. arene-alkene
  51586. photocycloadditions
  51587. cycloaddition
  51588. approach
  51589. membered
  51590. rings
  51591. trimethyl
  51592. cycloaddition
  51593. approaches
  51594. five-membered
  51595. rings
  51596. cycloaddition
  51597. allylsilanes
  51598. synthesis
  51599. bicycl
  51600. cycloaddition
  51601. reactions
  51602. transition-metal
  51603. 2-alkynyl
  51604. cycloadditions
  51605. triisopropyl
  51606. allyl
  51607. silane
  51608. unsaturat
  51609. dihydrofuranones
  51610. addition
  51611. lithiated
  51612. methoxyallene
  51613. isoquinolones
  51614. their
  51615. saturated
  51616. derivatives
  51617. 4-membered
  51618. systems
  51619. least
  51620. tellurium
  51621. piperidines
  51622. photoinduced
  51623. radical
  51624. cyclization
  51625. methoxy
  51626. phenylthio
  51627. propene
  51628. d1/d3
  51629. synthon
  51630. applicatio
  51631. 3'-dideoxy
  51632. 3'/45
  51633. 3-acyl-4-alkoxy-5-ar
  51634. 3-alkoxyacrolein
  51635. 3-alkoxyacrolein
  51636. organic
  51637. synthesis
  51638. 3-amino-2-azetidinon
  51639. 3-amino-2-hydroxybor
  51640. 3-amino-236-dideoxyh
  51641. 3-amino-2h-azirine
  51642. 3-amino-2h-azirine
  51643. synthons
  51644. alpha
  51645. alpha
  51646. isubstituted
  51647. 3-aryl-1-propyl
  51648. 3-benzothiopyrylium
  51649. 3-benzothiopyrylium
  51650. salts
  51651. 3-butyn-2-one
  51652. 3-cyclohexene-12-dio
  51653. 3-cyclopropenecarbos
  51654. 3-formyl-d2-isoxazol
  51655. 3-heteroquadricyclan
  51656. 3-heteroquadricyclan
  51657. organic
  51658. synthesis
  51659. 3-hydroxy-2-pyrone
  51660. 3-imino-12-oxazetidi
  51661. 3-iminodiaziridines
  51662. 3-iodothiophene
  51663. 3-lithioindole
  51664. 3-membered
  51665. 3-membered
  51666. systems
  51667. least
  51668. sulfur
  51669. 3-methanoamino
  51670. 3-methylcyclohe
  51671. 3-nitro-56-dihydro-4
  51672. 3-oxo
  51673. 3-oxo
  51674. 3-imino-12-oxazetidi
  51675. 2-oxo-13-oxazetidine
  51676. 3-oxo
  51677. 3-iminodiaziridines
  51678. 3-oxo
  51679. imino-12-thiazedine
  51680. 1-oxides
  51681. 3-oxo-12-diazetidine
  51682. 3-oxo-12-diazetidine
  51683. 2-oxo
  51684. 24-dioxo-13-diazetid
  51685. 3-oxocyclopentenes
  51686. stituent
  51687. 3-substituted
  51688. 3-sulfolenes
  51689. 3-ylidene
  51690. 3.1.0
  51691. 3.1.1
  51692. 3.2.0
  51693. 3.2.1
  51694. 3.2.1.0
  51695. 3.2.2
  51696. 3.3.0
  51697. 3.3.0.028
  51698. 3.3.1
  51699. 3.3.3
  51700. cyclazines
  51701. pyrido
  51702. 216-d
  51703. quinolizines
  51704. 30127
  51705. 30168
  51706. 30925
  51707. 31169
  51708. 31183
  51709. 31430
  51710. 321-kl
  51711. 32127
  51712. sigmatropic
  51713. rearrangements
  51714. method
  51715. organofluorine
  51716. sigmatropic
  51717. rearrangements
  51718. fluorocarbanions
  51719. 33147
  51720. 334455
  51721. 334455-hexamethyl-12
  51722. 334455-hexamethyl-12
  51723. methylene
  51724. cyclopentane
  51725. novel
  51726. probe
  51727. 34-differentially
  51728. 34-dihydroazetidines
  51729. 34-dihydroisoquinoli
  51730. 34-methamino
  51731. 34111
  51732. 34179
  51733. butyl
  51734. benzoquinone
  51735. cleaves
  51736. vicina
  51737. 35-pyrazolidinedione
  51738. 351675
  51739. 36-dihydrothiazine-1
  51740. 361109
  51741. 361279
  51742. 36135
  51743. 36161
  51744. 361683
  51745. 361901
  51746. 37-dibenzyloxy-48-di
  51747. 371047
  51748. 371453
  51749. 371825
  51750. 37191
  51751. 381339
  51752. 381541
  51753. 391013
  51754. 391215
  51755. 39123
  51756. 391417
  51757. 39173
  51758. 3:4-fused
  51759. 3a-hydroxy-15-ripper
  51760. azepines
  51761. related
  51762. systems
  51763. photoinduced
  51764. expansio
  51765. indole
  51766. 3h-pyrazoles
  51767. 3h-pyrroles
  51768. cycloadditions
  51769. amino
  51770. imino
  51771. thieno
  51772. benzo
  51773. cycloaddition
  51774. reaction
  51775. silyl
  51776. ethers
  51777. having
  51778. cycloadditions
  51779. cycloadditions
  51780. cycloaddition
  51781. reaction
  51782. total
  51783. synthesis
  51784. eight
  51785. membered
  51786. cyclic
  51787. nitrones
  51788. synthesis
  51789. reactivity
  51790. review
  51791. 4-acetoxyazeidinones
  51792. 4-alkoxy
  51793. 4-alkoxycarbonyloxaz
  51794. 4-alkyl
  51795. 4-dimethylaminopyrid
  51796. 4-dimethylaminopyrid
  51797. super
  51798. acylation
  51799. alkylation
  51800. catalyst
  51801. 4-dimethylaninopyrid
  51802. 4-dimethylaninopyrid
  51803. highly
  51804. active
  51805. acylation
  51806. agent
  51807. 4-iminodihydroazetes
  51808. 4-membered
  51809. 4-membered
  51810. systems
  51811. least
  51812. sulfur
  51813. 4-methoxybenzoate
  51814. 4-methoxybenzoates
  51815. 4-oxo
  51816. 4-oxo
  51817. 4-iminodihydroazetes
  51818. 4-oxo-16-dialkynyl
  51819. 4-oxo-16-enynyl
  51820. 4.1.0
  51821. 4.2.0
  51822. 4.2.0.0
  51823. 4.2.1
  51824. 4.3.0
  51825. 4.4.1
  51826. 4/nabh4
  51827. 40105
  51828. 401093
  51829. 401433
  51830. 401931
  51831. 40s24
  51832. 41115
  51833. 41135
  51834. 42136
  51835. 42335
  51836. 432873
  51837. 44'-bi
  51838. cyclobutene-12-dione
  51839. biquaryls
  51840. 44-disubstituted
  51841. 44854
  51842. 45-dihydro-5-oxo-13
  51843. 4507t
  51844. 45151
  51845. 45185
  51846. 461040
  51847. 461092
  51848. 461167
  51849. 46145
  51850. 46169
  51851. 46179
  51852. 47134
  51853. 47148
  51854. 47163
  51855. 47167
  51856. 481055
  51857. 48107
  51858. 481125
  51859. 48177
  51860. 491001
  51861. 491009
  51862. 491021
  51863. 491049
  51864. 491068
  51865. 491069
  51866. 491085
  51867. 491105
  51868. 491135
  51869. 491169
  51870. 491187
  51871. 491241
  51872. 491251
  51873. 491291
  51874. 491307
  51875. 491329
  51876. 49137
  51877. 491385
  51878. 491423
  51879. 49153
  51880. 49163
  51881. 49183
  51882. 49197
  51883. 49467
  51884. 4h-12-oxazetes
  51885. 4h-13-dithiins
  51886. 4h-13-oxazetes
  51887. acetyl
  51888. methyl
  51889. nitro
  51890. phenyl
  51891. pyridazinone
  51892. versati
  51893. acetyl
  51894. methyl
  51895. nitro
  51896. phenyl
  51897. pyridazinone
  51898. versati
  51899. closure
  51900. formylbenzoyl
  51901. radical
  51902. methylene
  51903. cyclopentenones
  51904. formal
  51905. cycloadduc
  51906. 5'-dimethoxybenzoin
  51907. 5'-epi-tunicamycin-v
  51908. 5'-phosphates
  51909. 5-alkylidenecyclopen
  51910. 5-amino-24-pentadien
  51911. 5-exo
  51912. 5-exo-trig
  51913. 5-hexenyl
  51914. 5-hydroxyindoles
  51915. 5-membered
  51916. 5-membered
  51917. tellurium
  51918. heteroarenes
  51919. 5.3.0
  51920. 5.3.1
  51921. 5.4.0
  51922. 5.4.0.026
  51923. 501087
  51924. 50138
  51925. 50180
  51926. 510-dideaza-5678-tet
  51927. 511-methanomorphanth
  51928. 511007
  51929. 511089
  51930. 51178
  51931. 521012
  51932. 521081
  51933. 521184
  51934. 521203
  51935. 52138
  51936. 52189
  51937. dihydro
  51938. pyridinones
  51939. cyclizations
  51940. 56-dihydro-alpha-pyr
  51941. 56157
  51942. 57110
  51943. 57153
  51944. 57165
  51945. 59organic
  51946. 5theH
  51947. radical
  51948. carbocyclizations
  51949. strategy
  51950. methyltetracyclo
  51951. 4.2.0.0
  51952. octane
  51953. bridged
  51954. 3.3.3
  51955. 6-endo
  51956. 6-endo-dig
  51957. 6-endo-dig
  51958. 6-endo-dig
  51959. radical
  51960. carbocyclizations
  51961. strategy
  51962. 6-endo-trig
  51963. 6-endo-trig
  51964. radical
  51965. cyclizations
  51966. synthetic
  51967. approaches
  51968. 6-heteropentafulvene
  51969. 6-membered
  51970. 6-membered
  51971. tellurium
  51972. heteroarenes
  51973. 6-substituted
  51974. 6.2.1.038
  51975. 61377
  51976. 61441
  51977. disubstituted
  51978. isoxazoles
  51979. disubstituted
  51980. 6h-pyrido
  51981. 6li-15n
  51982. 7-deoxyprekinamycin@
  51983. 8-catalyzed@
  51984. clerici
  51985. porta
  51986. milan
  51987. reductive
  51988. concise
  51989. synthesis
  51990. anthraquinone
  51991. portion
  51992. dynemici@
  51993. convenient
  51994. synthesis
  51995. cyclopropanes
  51996. olefin
  51997. carb@
  51998. decade
  51999. research
  52000. phosphin-imine
  52001. chemistry@
  52002. facile
  52003. conversion
  52004. nitro
  52005. olefins
  52006. functionalised
  52007. hydro@
  52008. fontana
  52009. toniolo
  52010. chemistry
  52011. tryptophane
  52012. peptides@
  52013. methyl
  52014. tetrahydro
  52015. oxazepin
  52016. dioxepino
  52017. 7-azabicyclo
  52018. 7-deacetoxyalcyonin
  52019. 7-membered
  52020. telluri
  52021. heteroarenes
  52022. 7-oxabicyclo
  52023. 7-phosphanorbornene
  52024. 7.3.1
  52025. 71319
  52026. 73125
  52027. 77121
  52028. 77183
  52029. 78-epoxy-4-basmen-6
  52030. 78199
  52031. 8-endo
  52032. 8-endo
  52033. cyclization
  52034. alkoxycarbonyl
  52035. methyl
  52036. radicals
  52037. generat
  52038. 8-membered
  52039. 80125
  52040. 81-bc
  52041. 81149
  52042. 85771
  52043. 86197
  52044. 87381
  52045. 87674
  52046. 8885s
  52047. bromo
  52048. bromomagnesium
  52049. methylene
  52050. fluorene
  52051. tetrahydrofuran
  52052. 9-borabicyclo
  52053. 9-fluorenylmethy
  52054. 9-hydroxycarbazoles
  52055. 9-oxo-9h
  52056. 9-oxo-9h-xanthenes
  52057. 9-oxo-9h-xanthenes
  52058. 9-xanthones
  52059. 9-oxo-9h
  52060. dibenzo
  52061. pyranes
  52062. 9-substituted
  52063. 9-xanthones
  52064. 9.3.3.0
  52065. 910-dihydroanthracen
  52066. 910-ethenoanthracene
  52067. 91059
  52068. 91089
  52069. 91333
  52070. 91617
  52071. 93552
  52072. 9517r
  52073. 971002
  52074. 9951006
  52075. amides
  52076. carbamates
  52077. ureas
  52078. iodosy
  52079. trialkoxyethyllithiu
  52080. stable
  52081. towards
  52082. fragmentation
  52083. shielded
  52084. vinyllithium
  52085. example
  52086. quantification
  52087. mauger
  52088. chemistry
  52089. cyclic
  52090. alpha
  52091. imino
  52092. acids
  52093. chemist
  52094. catalyzed
  52095. diels-alder
  52096. reaction
  52097. 3-hydroxy-2-pyrone
  52098. carbene
  52099. adduct
  52100. iodine
  52101. brandstrom
  52102. principles
  52103. phase
  52104. transfer
  52105. catalysis
  52106. quate
  52107. brief
  52108. history
  52109. photoinduced
  52110. electron
  52111. transfer
  52112. relate
  52113. pratt
  52114. photochemistry
  52115. imines
  52116. chemical
  52117. societ
  52118. cascade
  52119. macrocyclisation
  52120. transannulation
  52121. approach
  52122. polyc
  52123. catalytic
  52124. enantioselective
  52125. synthesis
  52126. denopamine
  52127. usefu
  52128. catalytic
  52129. enantioselective
  52130. synthetic
  52131. route
  52132. importan
  52133. catalytic
  52134. method
  52135. asymmetric
  52136. nucleophilic
  52137. aromatic
  52138. catalytic
  52139. tellurium
  52140. process
  52141. transposition
  52142. allyl
  52143. chemical
  52144. approach
  52145. protein
  52146. synthesis
  52147. template-assem
  52148. chiral
  52149. scandium
  52150. catalyst
  52151. enantioselective
  52152. diels
  52153. alder
  52154. clerici
  52155. porta
  52156. milan
  52157. reductive
  52158. cobalt
  52159. catalyzed
  52160. entry
  52161. ergot
  52162. alkaloids
  52163. total
  52164. cobalt
  52165. catalyzed
  52166. method
  52167. homologation
  52168. alcohols
  52169. collet
  52170. tetrahedron
  52171. cyclotriveratrylenes
  52172. comined
  52173. synthetic
  52174. initio
  52175. study
  52176. chiral
  52177. oxazaborol
  52178. comparison
  52179. chloromethyl
  52180. iodomethyl
  52181. cyclopropan
  52182. comparison
  52183. methods
  52184. using
  52185. lithium
  52186. amine
  52187. birch
  52188. reduct
  52189. compilation
  52190. analysis
  52191. structural
  52192. distorted
  52193. compilation
  52194. references
  52195. formyl
  52196. anion
  52197. synthon
  52198. compilation
  52199. references
  52200. functional
  52201. anion
  52202. synth
  52203. compolation
  52204. references
  52205. formyl
  52206. anion
  52207. synthon
  52208. concise
  52209. convergent
  52210. synthesis
  52211. acetogenins
  52212. solamin
  52213. concise
  52214. stereocontrolled
  52215. thiazolium
  52216. ylide
  52217. approach
  52218. concise
  52219. synthesis
  52220. enantiomerically
  52221. taxane
  52222. c-ring
  52223. concise
  52224. synthesis
  52225. anthraquinone
  52226. portion
  52227. dynemici
  52228. concise
  52229. synthetic
  52230. route
  52231. cyclopentenes
  52232. cycloaddit
  52233. conformational
  52234. analysis
  52235. transition
  52236. metal
  52237. eta-1-acyl
  52238. convenient
  52239. alternative
  52240. route
  52241. trimethylsilylfluoro
  52242. convenient
  52243. economic
  52244. produce
  52245. anhydrous
  52246. hydrogen
  52247. convenient
  52248. versatile
  52249. route
  52250. stereoselective
  52251. convenient
  52252. approach
  52253. synthesis
  52254. benzo
  52255. phenanthri
  52256. convenient
  52257. preparation
  52258. trimethylsilyl
  52259. trifluoro
  52260. convenient
  52261. large
  52262. scale
  52263. synthesis
  52264. ethylenediamine
  52265. convenient
  52266. method
  52267. production
  52268. ortho
  52269. amino
  52270. convenient
  52271. method
  52272. radical
  52273. cyclization
  52274. aldol
  52275. convenient
  52276. method
  52277. synthesis
  52278. indole
  52279. acetic
  52280. convenient
  52281. rearrangement
  52282. phenylpyrrole
  52283. carboxaldehy
  52284. convenient
  52285. stereoselective
  52286. synthesis
  52287. tributylstannyl
  52288. convenient
  52289. stereoselective
  52290. synthesis
  52291. disubstituted
  52292. convenient
  52293. synthesis
  52294. cyclopropanes
  52295. olefin
  52296. convenient
  52297. synthesis
  52298. diversely
  52299. substituted
  52300. dimethyl
  52301. convenient
  52302. synthesis
  52303. halogenated
  52304. spiro
  52305. furanone
  52306. convenient
  52307. synthesis
  52308. retronecine
  52309. member
  52310. pyrrol
  52311. convenient
  52312. synthesis
  52313. substituted
  52314. pyrroles
  52315. esters
  52316. convenient
  52317. synthetic
  52318. method
  52319. amide
  52320. oxidation
  52321. convergent
  52322. stereocontrolled
  52323. synthetic
  52324. route
  52325. cornelis
  52326. laszlo
  52327. synthesis
  52328. supported
  52329. cyclization
  52330. tertiary
  52331. amines
  52332. captodative
  52333. cycloaddition
  52334. approach
  52335. cyclopentenes
  52336. metalladienes
  52337. cyclobutanone
  52338. based
  52339. tandem
  52340. radical
  52341. rearrangement
  52342. baxter
  52343. roberts
  52344. london
  52345. asymmetr
  52346. ryabov
  52347. application
  52348. cyclopal
  52349. ryabov
  52350. synthesis
  52351. cyclopalladated
  52352. complexes
  52353. meijere
  52354. cyclopropyl
  52355. building
  52356. decade
  52357. research
  52358. phosphin-imine
  52359. chemistry
  52360. density
  52361. functional
  52362. study
  52363. stereocontrol
  52364. sharp
  52365. diastereoselective
  52366. aldol
  52367. reactions
  52368. chiral
  52369. aldehydes
  52370. dramatic
  52371. effect
  52372. catalytic
  52373. amount
  52374. simmo
  52375. dramatic
  52376. ligand
  52377. effect
  52378. relative
  52379. reactivities
  52380. function
  52381. highly
  52382. efficient
  52383. chiral
  52384. chiral
  52385. controller
  52386. efraty
  52387. cyclobutadienemetal
  52388. complexes
  52389. chemical
  52390. cockerill
  52391. harrison
  52392. mechanisms
  52393. elimination
  52394. kluge
  52395. heterocycles
  52396. synthesis
  52397. dioxaspi
  52398. facially
  52399. selective
  52400. protonation
  52401. controls
  52402. stereochemistr
  52403. facile
  52404. access
  52405. allyl
  52406. benzyl
  52407. cephems
  52408. reduct
  52409. facile
  52410. chemoselective
  52411. reduction
  52412. azide
  52413. amine
  52414. facile
  52415. selective
  52416. oxidation
  52417. sulfides
  52418. sulfones
  52419. facile
  52420. stereoselective
  52421. synthesis
  52422. arylethers
  52423. facile
  52424. approach
  52425. polysubstituted
  52426. chiral
  52427. dihydrofurans
  52428. facile
  52429. conversion
  52430. nitro
  52431. olefins
  52432. functionalised
  52433. hydro
  52434. facile
  52435. conversion
  52436. nitro
  52437. olefins
  52438. functionalized
  52439. hydro
  52440. facile
  52441. method
  52442. transformation
  52443. acetals
  52444. ketals
  52445. facile
  52446. synthesis
  52447. aldehyde
  52448. enamines
  52449. yield
  52450. facile
  52451. synthesis
  52452. pyrazolothiazoles
  52453. facile
  52454. preparation
  52455. disubstituted
  52456. furans
  52457. facile
  52458. preparation
  52459. amides
  52460. generation
  52461. trapping
  52462. facile
  52463. preparation
  52464. alumina
  52465. supported
  52466. chromium
  52467. reagen
  52468. facile
  52469. preparation
  52470. isopropoxyalkyl
  52471. amides
  52472. generati
  52473. facile
  52474. synthesis
  52475. substituted
  52476. isothiochroman
  52477. facile
  52478. synthesis
  52479. cyanohydrin
  52480. trimethylsilyl
  52481. ethers
  52482. facile
  52483. total
  52484. synthesis
  52485. cembrene
  52486. titanium
  52487. induced
  52488. flexible
  52489. rational
  52490. synthesis
  52491. substituted
  52492. triphenylen
  52493. flexible
  52494. route
  52495. bromo
  52496. alkylcyclopropenes
  52497. flexible
  52498. synthesis
  52499. polysubstituted
  52500. cyclopentanes
  52501. fontana
  52502. toniolo
  52503. chemistry
  52504. tryptophane
  52505. peptides
  52506. brown
  52507. roberts
  52508. royal
  52509. society
  52510. chemistry
  52511. barrett
  52512. graboski
  52513. conjugat
  52514. mclnnes
  52515. walter
  52516. wright
  52517. vining
  52518. general
  52519. efficient
  52520. synthesis
  52521. azicao
  52522. ketones
  52523. general
  52524. practical
  52525. synthesis
  52526. linear
  52527. conjugated
  52528. penta
  52529. general
  52530. cyclopentenone
  52531. synthesis
  52532. involving
  52533. rhodium
  52534. general
  52535. diastereoselective
  52536. synthesis
  52537. spiroacetals
  52538. relat
  52539. general
  52540. diastereoselective
  52541. synthesis
  52542. spiroacetals
  52543. using
  52544. general
  52545. method
  52546. synthesis
  52547. alkyl
  52548. substituted
  52549. general
  52550. method
  52551. synthesis
  52552. bridged
  52553. indole
  52554. alkaloi
  52555. general
  52556. strategy
  52557. increasing
  52558. molecular
  52559. complexity
  52560. photo
  52561. general
  52562. strategy
  52563. synthesis
  52564. cis-substituted
  52565. general
  52566. strategy
  52567. using
  52568. eta2-co2
  52569. acetylene
  52570. complexes
  52571. general
  52572. strategy
  52573. using
  52574. acetylene
  52575. complexes
  52576. general
  52577. synthesis
  52578. substituted
  52579. cyclohex
  52580. enones
  52581. general
  52582. synthetic
  52583. strategy
  52584. toward
  52585. amimocyclopentitiol
  52586. davidson
  52587. hodgson
  52588. howells
  52589. warren
  52590. haines
  52591. recent
  52592. developments
  52593. haines
  52594. methods
  52595. oxidation
  52596. organic
  52597. compounds
  52598. chimia
  52599. modern
  52600. synthetic
  52601. proced
  52602. highly
  52603. diastereoselective
  52604. enantioselective
  52605. highly
  52606. enantio
  52607. diastereoselective
  52608. aldol
  52609. reaction
  52610. highly
  52611. practical
  52612. route
  52613. prostaglandins
  52614. conjugate
  52615. highly
  52616. stereoselective
  52617. synthesis
  52618. a-glucosides
  52619. hydroxylation
  52620. cyclic
  52621. hydroxamic
  52622. acids
  52623. peroxide
  52624. oxida
  52625. kestner
  52626. immobilized
  52627. enzymes
  52628. meyers
  52629. aldrichimica
  52630. formamidines
  52631. meyers
  52632. mihelich
  52633. angew
  52634. ichihara
  52635. synthesis
  52636. retro
  52637. diels
  52638. alder
  52639. strategy
  52640. general
  52641. synthesis
  52642. substituted
  52643. cyclohex
  52644. enones@
  52645. highly
  52646. efficient
  52647. synthesis
  52648. b-substituted
  52649. seven
  52650. ichihara
  52651. synthesis
  52652. retro
  52653. diels
  52654. alder
  52655. strategy
  52656. krief
  52657. synthesis
  52658. synthetic
  52659. method
  52660. selective
  52661. cleavage
  52662. tetrahydropyranyl
  52663. strategy
  52664. macrocyclization
  52665. based
  52666. radical
  52667. selective
  52668. bromination
  52669. unsaturated
  52670. ketones@
  52671. efficient
  52672. synthesis
  52673. ethyl
  52674. carboline
  52675. carboxylate@
  52676. nickel-catalyzed
  52677. cross-coupling
  52678. reaction
  52679. between
  52680. palladium
  52681. catalyzed
  52682. synthesis
  52683. disubstituted
  52684. coum@
  52685. procedure
  52686. horner
  52687. wadsworth
  52688. emmons
  52689. olefination
  52690. lsilyl
  52691. triflate-promoted
  52692. annulation
  52693. n-ace
  52694. palladium
  52695. catalysed
  52696. cascade
  52697. cyclisation
  52698. friedel
  52699. crafts
  52700. practical
  52701. alternative
  52702. sulfonyl
  52703. activation
  52704. aziridines@
  52705. reagent
  52706. determining
  52707. optical
  52708. purities
  52709. diols
  52710. forma
  52711. ichihara
  52712. synthesis
  52713. retro
  52714. diels
  52715. alder
  52716. strategy
  52717. birch
  52718. williamson
  52719. homogeneous
  52720. hydrogenation
  52721. catal
  52722. fatiadi
  52723. synthesis
  52724. applications
  52725. tetracyan
  52726. fatiadi
  52727. synthesis
  52728. active
  52729. manganese
  52730. dioxide
  52731. fatiadi
  52732. synthesis
  52733. addition
  52734. cycloaddition
  52735. floyd
  52736. fritsch
  52737. borazaromatic
  52738. compounds
  52739. special
  52740. topics
  52741. electrochemistry
  52742. groups
  52743. synthetic
  52744. organic
  52745. electrochemistry
  52746. harper
  52747. klunder
  52748. ariaans
  52749. zwane
  52750. willi
  52751. kinetic
  52752. carbon
  52753. other
  52754. isotope
  52755. effects
  52756. cleava
  52757. galwey
  52758. compensation
  52759. effect
  52760. heterogeneous
  52761. catalysis
  52762. mukerjee
  52763. singh
  52764. synthesis
  52765. reactions
  52766. kjaer
  52767. molecular
  52768. weight
  52769. sulphur
  52770. containing
  52771. compounds
  52772. krief
  52773. tetrahedron
  52774. syntheses
  52775. tetraheteroful
  52776. krief
  52777. synthesis
  52778. synthetic
  52779. rusanov
  52780. chemistry
  52781. unsub
  52782. weiss
  52783. heterocycles
  52784. labert
  52785. heterocycl
  52786. chemistry
  52787. laser
  52788. flash
  52789. photolysis
  52790. study
  52791. carbonyl
  52792. ylides
  52793. arylchl
  52794. ligand
  52795. assisted
  52796. claisen
  52797. rearrangement
  52798. marquet
  52799. aspects
  52800. chemistry
  52801. biotin
  52802. mckillop
  52803. applications
  52804. mechanistic
  52805. study
  52806. oleate
  52807. autoxidation
  52808. competing
  52809. peroxyl
  52810. medicinal
  52811. chemistry
  52812. study
  52813. account
  52814. angiotensi
  52815. method
  52816. stereoselective
  52817. construction
  52818. 4-alkoxy
  52819. convenient
  52820. synthesis
  52821. functionalized
  52822. methyl
  52823. efficient
  52824. route
  52825. pharmacophore
  52826. enedi
  52827. facile
  52828. synthesis
  52829. carboxylic
  52830. anhydrides
  52831. inexpensive
  52832. practical
  52833. oxidation
  52834. sulfides
  52835. method
  52836. selective
  52837. cleavage
  52838. tetrahydropyranyl
  52839. regioselective
  52840. ketal
  52841. claisen
  52842. rearrangement
  52843. promoted
  52844. mitra
  52845. synthesis
  52846. prostaglandins
  52847. wiley
  52848. lnterscience
  52849. model
  52850. radical
  52851. electrophilic
  52852. hydroxylation
  52853. model
  52854. influence
  52855. media
  52856. photochemica
  52857. modified
  52858. synthesis
  52859. hydroxyaryl
  52860. aldehydes
  52861. modular
  52862. approach
  52863. ligand
  52864. design
  52865. asymmetric
  52866. allylic
  52867. multicomponent
  52868. redox
  52869. system
  52870. accounts
  52871. first
  52872. nozaki-
  52873. belder
  52874. cyclic
  52875. acetals
  52876. aldoses
  52877. aldosides
  52878. pudovik
  52879. konovalova
  52880. burnaeva
  52881. synthesis
  52882. volkov
  52883. nikol'skaya
  52884. alpha
  52885. cyanoacetylenes
  52886. route
  52887. arenes
  52888. application
  52889. facile
  52890. synthesi
  52891. cycloaddition
  52892. method
  52893. application
  52894. alkoxyiodination
  52895. nitratoiodination
  52896. olefins
  52897. approach
  52898. vinylimino
  52899. phosphoranes
  52900. selective
  52901. bromination
  52902. unsaturated
  52903. ketones
  52904. annulation
  52905. sequence
  52906. using
  52907. trimethylstannyl
  52908. unsaturated
  52909. application
  52910. modified
  52911. peptides
  52912. peptidomimetics
  52913. approach
  52914. adamantane
  52915. rearrangements
  52916. approach
  52917. alkyl
  52918. oxoquinoline
  52919. acetates
  52920. triphen
  52921. approach
  52922. fluoropyrroles
  52923. based
  52924. michael
  52925. approach
  52926. 1-arylnaphthalene
  52927. lignans
  52928. utilizing
  52929. approach
  52930. synthesis
  52931. fluoropyrrole
  52932. derivativ
  52933. approach
  52934. synthesis
  52935. glycosides
  52936. approach
  52937. synthesis
  52938. arylakyl
  52939. aminoalcohols
  52940. convenient
  52941. synthesis
  52942. methyl
  52943. oxoalkanoates
  52944. coupling
  52945. reaction
  52946. vinyl
  52947. esters
  52948. aldehydes
  52949. catal
  52950. cyclization
  52951. reaction
  52952. cascade
  52953. stereo
  52954. cyclopentannulation
  52955. approach
  52956. bicyclo
  52957. 3.3.0
  52958. octenes
  52959. domino
  52960. synthesis
  52961. polyfunctionalized
  52962. pentasubstitute
  52963. efficient
  52964. synthesis
  52965. ethyl
  52966. carboline
  52967. carboxylate
  52968. entry
  52969. carbanion
  52970. chemistry
  52971. selectivities
  52972. entry
  52973. unsubstituted
  52974. acyltetramic
  52975. acids
  52976. facile
  52977. synthesis
  52978. substituted
  52979. butadiene
  52980. derivat
  52981. general
  52982. stereoselective
  52983. method
  52984. synthesis
  52985. highly
  52986. efficient
  52987. synthesis
  52988. conjugated
  52989. nitrocycloalk
  52990. highly
  52991. enantioselective
  52992. synthetic
  52993. route
  52994. p-chiral
  52995. method
  52996. preparation
  52997. n-methoxy-n-methylam
  52998. method
  52999. preparation
  53000. tetrazoles
  53001. nitriles
  53002. method
  53003. synthesis
  53004. silanes
  53005. review
  53006. method
  53007. synthesis
  53008. cyclopentenones
  53009. method
  53010. radical
  53011. chemistry
  53012. generation
  53013. radicals
  53014. methodology
  53015. synthesis
  53016. acylaminocinnamates
  53017. synthesis
  53018. unsymmetrical
  53019. disulfides
  53020. reaction
  53021. flask
  53022. ramberg
  53023. backlund
  53024. reaction
  53025. palladium
  53026. catalyzed
  53027. synthesis
  53028. disubstituted
  53029. platform
  53030. designing
  53031. ligands
  53032. asymmetric
  53033. inductio
  53034. example
  53035. cyclopropanation
  53036. radical
  53037. chemi
  53038. reaction
  53039. chloro
  53040. chlorosulfenyl
  53041. ketones
  53042. facile
  53043. rearrangement
  53044. oxetane
  53045. taxoids
  53046. organometallic
  53047. reactions
  53048. organic
  53049. synthesis
  53050. route
  53051. furanones
  53052. ruthenium
  53053. catalysed
  53054. oxidat
  53055. route
  53056. chiral
  53057. epoxy
  53058. butane
  53059. diols
  53060. route
  53061. chiral
  53062. pyrrolidines
  53063. radical
  53064. cyclisation
  53065. route
  53066. chiral
  53067. pyrrolidines
  53068. radical
  53069. cyclization
  53070. route
  53071. highly
  53072. substituted
  53073. pyrrol
  53074. route
  53075. monosubstituted
  53076. thioamides
  53077. review
  53078. route
  53079. allenylphenols
  53080. route
  53081. phenanthrene
  53082. derivatives
  53083. route
  53084. isoindole
  53085. nucleus
  53086. furan
  53087. pyrrole
  53088. sequential
  53089. alkoxy
  53090. radical
  53091. fragmentation
  53092. hydroxyke
  53093. series
  53094. nitrene-induced
  53095. aromatic
  53096. rearrangements
  53097. stereospecific
  53098. annulation
  53099. reaction
  53100. strategy
  53101. lewis
  53102. catalyzed
  53103. cyclopropanation
  53104. thiofuranosides
  53105. regioselective
  53106. synthesis
  53107. trimethylsilyl
  53108. dihydrofurans
  53109. synthesis
  53110. formyl
  53111. sulfones
  53112. synthesis
  53113. cyclopenta
  53114. phenanthrene
  53115. involving
  53116. cycli
  53117. synthesis
  53118. trimethylsilyl
  53119. dihydrofurans
  53120. trimeth
  53121. synthetic
  53122. method
  53123. methylcarbapenems
  53124. utilizing
  53125. titanium
  53126. silica
  53127. catalyst
  53128. expoxidation
  53129. non-H
  53130. nickel
  53131. catalyst
  53132. arylation
  53133. vinylation
  53134. lithiu
  53135. nickel
  53136. complex
  53137. photochemical
  53138. activation
  53139. carbon
  53140. nonbiomimetic
  53141. approach
  53142. total
  53143. synthesis
  53144. steroids
  53145. novel
  53146. access
  53147. hydrindan
  53148. derivatives
  53149. palladium
  53150. mediate
  53151. novel
  53152. convenient
  53153. synthesis
  53154. 2-aryl-4methylenetet
  53155. novel
  53156. efficient
  53157. approach
  53158. synthesis
  53159. amino
  53160. novel
  53161. efficient
  53162. generation
  53163. functionalized
  53164. vinylcopp
  53165. novel
  53166. efficient
  53167. method
  53168. oxidizing
  53169. sulfides
  53170. sulfo
  53171. novel
  53172. stereoselective
  53173. spiroannelation
  53174. facile
  53175. access
  53176. novel
  53177. approach
  53178. disubstituted
  53179. dihydro
  53180. phenylquin
  53181. novel
  53182. approach
  53183. cephalosporins
  53184. allenyl
  53185. azetidinones
  53186. novel
  53187. approach
  53188. polycyclic
  53189. indolic
  53190. systems
  53191. novel
  53192. approach
  53193. synthesis
  53194. taxol
  53195. synthesis
  53196. novel
  53197. asymmetric
  53198. pummerer
  53199. reaction
  53200. induced
  53201. ethoxy
  53202. vinyl
  53203. novel
  53204. carbonyl
  53205. transformation
  53206. using
  53207. novel
  53208. cycloalkylation
  53209. 17-enynes
  53210. stabilized
  53211. novel
  53212. cyclopentane
  53213. annulation
  53214. cycloaddition
  53215. novel
  53216. double
  53217. friedel
  53218. crafts
  53219. reaction
  53220. entry
  53221. novel
  53222. enantioselective
  53223. synthesis
  53224. biotin
  53225. novel
  53226. fluoride
  53227. mediated
  53228. olefination
  53229. electron
  53230. defici
  53231. novel
  53232. intramolecular
  53233. silyl
  53234. nitronate
  53235. cycloaddition
  53236. route
  53237. novel
  53238. method
  53239. chirospecific
  53240. synthesis
  53241. disubstitut
  53242. novel
  53243. method
  53244. synthesis
  53245. fluoroketones
  53246. novel
  53247. palladium
  53248. catalyzed
  53249. cycloaddition
  53250. 27-octadienyl
  53251. novel
  53252. preparation
  53253. scalemic
  53254. n-methyl-a-amino
  53255. acids
  53256. novel
  53257. rearrangement
  53258. aminoaryl
  53259. imidazoles
  53260. novel
  53261. route
  53262. diastereomerically
  53263. alkene
  53264. dipeptide
  53265. novel
  53266. stereoselective
  53267. synthesis
  53268. substituted
  53269. g-butyrolac
  53270. novel
  53271. synthesis
  53272. substituted
  53273. piperidones
  53274. novel
  53275. synthesis
  53276. spiro
  53277. substituted
  53278. azetidines
  53279. novel
  53280. synthesis
  53281. homologated
  53282. allylic
  53283. alcohols
  53284. using
  53285. novel
  53286. synthesis
  53287. lactones
  53288. oxidation
  53289. alicyclic
  53290. novel
  53291. synthesis
  53292. squaric
  53293. esters
  53294. novel
  53295. mediated
  53296. indole
  53297. synthesis
  53298. novel
  53299. transformation
  53300. involving
  53301. selective
  53302. formation
  53303. novel
  53304. trimethylsilyl
  53305. triflate-promoted
  53306. annulation
  53307. n-ace
  53308. novel
  53309. trimethylsilyl
  53310. triflate-promoted
  53311. annulation
  53312. n-ace
  53313. nuclear
  53314. magnetic
  53315. resonance
  53316. spectroscopic
  53317. technique
  53318. thiols
  53319. organic
  53320. chemistry
  53321. sulfur
  53322. thiones
  53323. organic
  53324. chemistry
  53325. sulfur
  53326. plenum
  53327. chemoselective
  53328. conversion
  53329. silyl
  53330. protected
  53331. conversion
  53332. methoxybenzyl
  53333. ethers
  53334. methoxy
  53335. kozikowski
  53336. wetter
  53337. synthesis
  53338. transition
  53339. kozikowski
  53340. wetter
  53341. synthesis
  53342. transition
  53343. krapcho
  53344. synthesis
  53345. synthesis
  53346. carbocyclic
  53347. marchand
  53348. reactions
  53349. carbenes
  53350. groups
  53351. chemi
  53352. padwa
  53353. angew
  53354. intramolecular
  53355. padwa
  53356. photochemistry
  53357. carbon
  53358. nitrogen
  53359. double
  53360. patchornik
  53361. kraus
  53362. pelter
  53363. reductions
  53364. involving
  53365. diborane
  53366. pfenninger
  53367. synthesis
  53368. asymmetric
  53369. epoxidation
  53370. practical
  53371. alternative
  53372. sulfonyl
  53373. activation
  53374. aziridines
  53375. practical
  53376. asymmetric
  53377. synthesis
  53378. novel
  53379. topically
  53380. active
  53381. practical
  53382. guide
  53383. first
  53384. order
  53385. multiplet
  53386. analysis
  53387. practical
  53388. guide
  53389. lanthanide
  53390. shift
  53391. reagents
  53392. practical
  53393. method
  53394. synthesis
  53395. l-a-amino
  53396. acids
  53397. practical
  53398. procedure
  53399. elaboration
  53400. amines
  53401. primer
  53402. fourier
  53403. transform
  53404. spectroscopy
  53405. prostaglandin
  53406. synthesis
  53407. qualitative
  53408. valence-bond
  53409. approach
  53410. organic
  53411. reactivity
  53412. battersby
  53413. recent
  53414. researches
  53415. biosynthesis
  53416. natur
  53417. katritzky
  53418. topsom
  53419. infrared
  53420. intensities
  53421. guide
  53422. rabenau
  53423. angew
  53424. rapid
  53425. total
  53426. synthesis
  53427. ellagitannin
  53428. rassat
  53429. stereochemistry
  53430. dissolving
  53431. metal
  53432. reduction
  53433. reaction
  53434. cascade
  53435. leading
  53436. 16-didehydro
  53437. annulene
  53438. 15-de
  53439. reagent
  53440. determining
  53441. optical
  53442. purities
  53443. diols
  53444. forma
  53445. reagent
  53446. determining
  53447. optical
  53448. purities
  53449. diols
  53450. forma
  53451. regioselective
  53452. annulation
  53453. butenolides
  53454. total
  53455. synthes
  53456. regioselective
  53457. entry
  53458. azirino
  53459. indole
  53460. epoxidation
  53461. regioselective
  53462. tandem
  53463. reduction
  53464. wittig
  53465. horner
  53466. reaction
  53467. reinvestigation
  53468. alkylation
  53469. monosubstituted
  53470. remarkable
  53471. cyclopropanation
  53472. total
  53473. synthesis
  53474. myrocin
  53475. remarkable
  53476. effect
  53477. silyl
  53478. substitution
  53479. electrocyclizat
  53480. remarkable
  53481. substituent
  53482. effect
  53483. enantioselectivity
  53484. review
  53485. synthetic
  53486. review
  53487. review
  53488. martin
  53489. barnikow
  53490. thiocar
  53491. review
  53492. solov'yanov
  53493. beletskaya
  53494. review
  53495. collet
  53496. tetrahedron
  53497. tetrahedron
  53498. repor
  53499. review
  53500. ichihara
  53501. synthesis
  53502. retro
  53503. diels
  53504. alder
  53505. review
  53506. fatiadi
  53507. synthesis
  53508. addition
  53509. cycload
  53510. review
  53511. fatiadi
  53512. synthesis
  53513. classical
  53514. permang
  53515. review
  53516. fatiadi
  53517. synthesis
  53518. applications
  53519. review
  53520. mukerjee
  53521. heterocycles
  53522. azlactones
  53523. review
  53524. tanikaga
  53525. tanaka
  53526. synth
  53527. review
  53528. kamal
  53529. sattur
  53530. heterocycles
  53531. chloros
  53532. review
  53533. katoh
  53534. nishio
  53535. kashima
  53536. heterocycles
  53537. review
  53538. campbell
  53539. synthesis
  53540. review
  53541. leval
  53542. heterocycl
  53543. compds
  53544. trans
  53545. review
  53546. maercker
  53547. theis
  53548. review
  53549. maercker
  53550. angew
  53551. ether
  53552. review
  53553. katritzky
  53554. marson
  53555. allah
  53556. heterocyc
  53557. review
  53558. katritzky
  53559. ostercamp
  53560. yousaf
  53561. tetrahed
  53562. review
  53563. katritzky
  53564. allah
  53565. marson
  53566. heterocyc
  53567. review
  53568. kertes
  53569. extrac
  53570. review
  53571. survey
  53572. radical
  53573. mediated
  53574. cyclization
  53575. review
  53576. frank
  53577. phosphorus
  53578. sulphur
  53579. review
  53580. abboud
  53581. kamlet
  53582. examination
  53583. review
  53584. abdulla
  53585. ultrasound
  53586. organic
  53587. synthesis
  53588. review
  53589. edward
  53590. whizz
  53591. metal
  53592. sulfur
  53593. review
  53594. acheson
  53595. morrin
  53596. hydroxypyrroles
  53597. hydroxyindoles
  53598. review
  53599. ackroyd
  53600. scheinmann
  53601. synthesis
  53602. leukotriene
  53603. review
  53604. bloodworth
  53605. chemistry
  53606. saturated
  53607. bicycl
  53608. review
  53609. cilento
  53610. membered
  53611. peroxides
  53612. review
  53613. determination
  53614. chemi
  53615. excitation
  53616. yields
  53617. review
  53618. zinner
  53619. determination
  53620. activation
  53621. paramet
  53622. review
  53623. waldemar
  53624. curci
  53625. ruggero
  53626. edwards
  53627. dioxiranes
  53628. review
  53629. waldemar
  53630. grabowski
  53631. wilson
  53632. marshall
  53633. review
  53634. adams
  53635. richard
  53636. metal
  53637. cluster
  53638. complexes
  53639. containing
  53640. review
  53641. addition
  53642. reaction
  53643. epoxy
  53644. compounds
  53645. esters
  53646. review
  53647. adlington
  53648. barrett
  53649. recent
  53650. applications
  53651. review
  53652. frank
  53653. phosphorus
  53654. sulphur
  53655. review
  53656. groot
  53657. review
  53658. akitt
  53659. multinuclear
  53660. studies
  53661. aluminum
  53662. compound@
  53663. review
  53664. allen
  53665. kennard
  53666. taylor
  53667. systematic
  53668. analysis
  53669. review
  53670. anderson
  53671. anderson
  53672. sydia
  53673. trimethylsilyldiazom
  53674. review
  53675. arginine
  53676. histidine
  53677. trytophan
  53678. peptide
  53679. synthes
  53680. review
  53681. astruc
  53682. didier
  53683. transition
  53684. metal
  53685. radicals
  53686. chameleon
  53687. review
  53688. rockett
  53689. organomet
  53690. review
  53691. bailey
  53692. introduction
  53693. peptide
  53694. chemistry
  53695. review
  53696. bardin
  53697. yagupolskii
  53698. xenon
  53699. difluoride
  53700. review
  53701. bartmann
  53702. trost
  53703. selectivity
  53704. review
  53705. becker
  53706. synthesis
  53707. stilbenes
  53708. synthesi@
  53709. review
  53710. bentrude
  53711. phosphoranyl
  53712. radicals
  53713. reactive
  53714. interme@
  53715. review
  53716. bestmann
  53717. schmid
  53718. kisielowski
  53719. synthesis
  53720. review
  53721. groot
  53722. review
  53723. afanas'ev
  53724. dzhamanbaev
  53725. zaikov
  53726. derivativ
  53727. review
  53728. afzal
  53729. oriquat
  53730. biosynthesis
  53731. isoflavonoid
  53732. review
  53733. agababyan
  53734. gevorgyan
  53735. mndzhoyan
  53736. amino
  53737. review
  53738. agami
  53739. claude
  53740. mechanism
  53741. proline
  53742. catalyzed
  53743. review
  53744. silicon
  53745. containing
  53746. carbonyl
  53747. equivalents
  53748. review
  53749. peterson
  53750. reaction
  53751. synthesis
  53752. review
  53753. david
  53754. peterson
  53755. olefination
  53756. reaction
  53757. review
  53758. agrawal
  53759. carbon
  53760. flavonoids
  53761. studies
  53762. review
  53763. agrawal
  53764. rastogi
  53765. spectroscopy
  53766. review
  53767. aguero
  53768. alina
  53769. osborn
  53770. synthesis
  53771. routes
  53772. review
  53773. ahlberg
  53774. jonsall
  53775. engdahl
  53776. degenerate
  53777. carbocation
  53778. review
  53779. sakai
  53780. alkaloids
  53781. strychnos
  53782. review
  53783. akhmedov
  53784. karimov
  53785. shcherbakova
  53786. porshne
  53787. review
  53788. akhrem
  53789. chistovalova
  53790. vol'pim
  53791. splitti
  53792. review
  53793. akitt
  53794. multinuclear
  53795. studies
  53796. aluminum
  53797. compound
  53798. review
  53799. akiyama
  53800. bednarski
  53801. simon
  53802. review
  53803. talib
  53804. mahmoud
  53805. tashtoush
  53806. hasan
  53807. recent
  53808. advances
  53809. review
  53810. albert
  53811. annelation
  53812. pyrimidine
  53813. review
  53814. albini
  53815. alpegiani
  53816. photochemistry
  53817. review
  53818. albini
  53819. angelo
  53820. pietra
  53821. silvio
  53822. heterocyclic
  53823. oxides
  53824. review
  53825. albright
  53826. reactions
  53827. anion
  53828. equivalents
  53829. review
  53830. albright
  53831. structure
  53832. reactivity
  53833. organometa
  53834. review
  53835. alder
  53836. medium
  53837. bicyclic
  53838. compounds
  53839. intrab
  53840. review
  53841. alder
  53842. roger
  53843. intrabridgehead
  53844. chemistry
  53845. review
  53846. alder
  53847. roger
  53848. strain
  53849. effects
  53850. amine
  53851. basicities
  53852. review
  53853. aldoshin
  53854. spiropyrans
  53855. structural
  53856. features
  53857. review
  53858. alekseeva
  53859. yakhontov
  53860. reactions
  53861. pyridines
  53862. review
  53863. allen
  53864. annette
  53865. tidwell
  53866. thomas
  53867. fluorine
  53868. substitut
  53869. review
  53870. allen
  53871. christopher
  53872. regio
  53873. stereochemical
  53874. contro
  53875. review
  53876. allen
  53877. kennard
  53878. taylor
  53879. systematic
  53880. analysis
  53881. review
  53882. allen
  53883. whitten
  53884. david
  53885. photophysics
  53886. review
  53887. allen
  53888. biochemiexcitation
  53889. chemiluminescence
  53890. review
  53891. allenmark
  53892. chromatographic
  53893. enantioseparation
  53894. review
  53895. alpegiani
  53896. marco
  53897. bedeschi
  53898. angelo
  53899. giudici
  53900. franco
  53901. review
  53902. alpegiani
  53903. marco
  53904. bedeschi
  53905. angelo
  53906. perrone
  53907. ettore
  53908. review
  53909. photochemistry
  53910. alkyltransition
  53911. metal
  53912. review
  53913. altona
  53914. conformational
  53915. analysis
  53916. nucleic
  53917. acids
  53918. review
  53919. alves
  53920. chemical
  53921. ecology
  53922. social
  53923. behavior
  53924. review
  53925. amiya
  53926. bando
  53927. aconitum
  53928. alkaloids
  53929. alkaloids
  53930. review
  53931. amoore
  53932. theory
  53933. classification
  53934. review
  53935. anand
  53936. nitya
  53937. singh
  53938. jujhar
  53939. chemistry
  53940. lactam
  53941. acetal
  53942. review
  53943. anders
  53944. hayatsu
  53945. organic
  53946. compounds
  53947. meterorites
  53948. review
  53949. andersen
  53950. robertson
  53951. isotope
  53952. dilutio
  53953. review
  53954. anderson
  53955. organic
  53956. chemistry
  53957. review
  53958. anderson
  53959. anderson
  53960. sydia
  53961. trimethylsilyldiazom
  53962. review
  53963. angyal
  53964. composition
  53965. reducing
  53966. sugars
  53967. review
  53968. angyal
  53969. stephen
  53970. compiexes
  53971. metal
  53972. cations
  53973. review
  53974. anklam
  53975. margaretha
  53976. organic
  53977. sulfuranyl
  53978. radicals
  53979. review
  53980. anteunis
  53981. structure
  53982. conformation
  53983. mechanism
  53984. review
  53985. antipin
  53986. temperature
  53987. diffraction
  53988. review
  53989. antonakis
  53990. ketonucleosides
  53991. advances
  53992. review
  53993. antonova
  53994. ioganson
  53995. transition
  53996. metal
  53997. complexe
  53998. review
  53999. apsimon
  54000. total
  54001. synthesis
  54002. natural
  54003. product
  54004. review
  54005. apsimon
  54006. total
  54007. synthesis
  54008. natural
  54009. review
  54010. isoquinolinequinones
  54011. actinomycet
  54012. review
  54013. vicente
  54014. piiar
  54015. ochoa
  54016. carmen
  54017. heterocycles
  54018. review
  54019. arbuzov
  54020. nikonov
  54021. containing
  54022. heterocycles
  54023. review
  54024. arbuzov
  54025. zobova
  54026. addition
  54027. aliphatic
  54028. review
  54029. arginine
  54030. histidine
  54031. trytophan
  54032. peptide
  54033. synthes
  54034. review
  54035. arginine
  54036. histidine
  54037. trytophan
  54038. peptide
  54039. synthes
  54040. review
  54041. arkles
  54042. silane
  54043. coupling
  54044. agent
  54045. chemistry
  54046. silic
  54047. review
  54048. arkles
  54049. techniques
  54050. silylation
  54051. silicon
  54052. review
  54053. armentrout
  54054. beauchamp
  54055. chemistry
  54056. atomi
  54057. review
  54058. arnett
  54059. hofelich
  54060. schriver
  54061. carbocations
  54062. review
  54063. arseniyadis
  54064. kyler
  54065. addition
  54066. subst
  54067. review
  54068. arshinova
  54069. contemporary
  54070. ideas
  54071. about
  54072. conforma
  54073. review
  54074. artamkina
  54075. egorov
  54076. beletskaya
  54077. aspect
  54078. review
  54079. asakawa
  54080. chemical
  54081. constituents
  54082. hepaticae
  54083. review
  54084. drone
  54085. kausch
  54086. kroker
  54087. tawee
  54088. review
  54089. group
  54090. heterobenzenes
  54091. arsabenzene
  54092. review
  54093. arthur
  54094. thermochromic
  54095. distibines
  54096. review
  54097. astruc
  54098. hamon
  54099. mandon
  54100. moulines
  54101. aspects
  54102. review
  54103. astruc
  54104. organo
  54105. complexes
  54106. aromatic
  54107. compound
  54108. review
  54109. astruc
  54110. didier
  54111. transition
  54112. metal
  54113. radicals
  54114. chameleon
  54115. review
  54116. astruc
  54117. didier
  54118. transition
  54119. metal
  54120. radicals
  54121. chameleon
  54122. review
  54123. crossroads
  54124. chemistry
  54125. immunology
  54126. catal
  54127. review
  54128. atherton
  54129. sheppard
  54130. solid
  54131. phase
  54132. peptide
  54133. synthes
  54134. review
  54135. rahman
  54136. choudhary
  54137. muhammad
  54138. iqbal
  54139. purine
  54140. review
  54141. rahman
  54142. qureshi
  54143. munawer
  54144. applications
  54145. review
  54146. rahman
  54147. sultana
  54148. synthetic
  54149. approaches
  54150. review
  54151. attygalle
  54152. morgan
  54153. chemicals
  54154. glands
  54155. review
  54156. atwood
  54157. davies
  54158. incluhion
  54159. compounds
  54160. volume
  54161. review
  54162. atwood
  54163. davies
  54164. inclusion
  54165. compounds
  54166. volume
  54167. review
  54168. aurich
  54169. guenter
  54170. chemistry
  54171. vinyl
  54172. nitroxid
  54173. review
  54174. alcermark
  54175. symposium
  54176. synthetic
  54177. review
  54178. lipshutz
  54179. synthesis
  54180. applications
  54181. review
  54182. halton
  54183. stang
  54184. review
  54185. feringa
  54186. photo
  54187. oxidat
  54188. review
  54189. rockett
  54190. organomet
  54191. review
  54192. rockett
  54193. organomet
  54194. review
  54195. harvey
  54196. review
  54197. venepalli
  54198. agosta
  54199. review
  54200. joshi
  54201. pelletier
  54202. heterocycles
  54203. review
  54204. abdou
  54205. daboun
  54206. hetrocyc
  54207. review
  54208. babichev
  54209. kovtunenko
  54210. tyltin
  54211. advances
  54212. review
  54213. backvall
  54214. palladium
  54215. selective
  54216. oxidation
  54217. review
  54218. backvall
  54219. metal
  54220. mediated
  54221. additions
  54222. conjugat
  54223. review
  54224. badanyan
  54225. melikyan
  54226. mkrtchyan
  54227. introd
  54228. review
  54229. badanyan
  54230. voskanyan
  54231. chobanyan
  54232. copper
  54233. review
  54234. baeckvsll
  54235. stereoselective
  54236. annulations
  54237. review
  54238. recent
  54239. synthetic
  54240. studies
  54241. nitrogen
  54242. review
  54243. baerheim
  54244. svendsen
  54245. verpoorte
  54246. chromatography
  54247. review
  54248. baggott
  54249. selectivity
  54250. search
  54251. review
  54252. bagrii
  54253. saginaev
  54254. unsaturated
  54255. adamantane
  54256. review
  54257. bailey
  54258. introduction
  54259. peptide
  54260. chemistry
  54261. review
  54262. baird
  54263. functionalized
  54264. cyclopropenes
  54265. synthe
  54266. review
  54267. baizer
  54268. organic
  54269. electrochemistry
  54270. review
  54271. baizer
  54272. recent
  54273. developments
  54274. orgamic
  54275. synthesis
  54276. review
  54277. bakers
  54278. yeast
  54279. mediated
  54280. transformation
  54281. organic
  54282. review
  54283. bakhmutov
  54284. galakhov
  54285. spectroscopy
  54286. review
  54287. balaban
  54288. fischer
  54289. dinculescu
  54290. dorofeenko
  54291. review
  54292. balch
  54293. metallomacrocycles
  54294. novel
  54295. amphoteric
  54296. review
  54297. balci
  54298. metin
  54299. sutbeyaz
  54300. yasar
  54301. secen
  54302. hasan
  54303. conduritols
  54304. review
  54305. baldwin
  54306. perlmutter
  54307. bridged
  54308. capped
  54309. fenced
  54310. review
  54311. ballah
  54312. jeyaraman
  54313. chandrasekaran
  54314. synthesis
  54315. review
  54316. ballester
  54317. perchloro
  54318. organic
  54319. chemistry
  54320. structures
  54321. review
  54322. ballini
  54323. petrini
  54324. marotta
  54325. righi
  54326. recent
  54327. progre
  54328. review
  54329. bannemann
  54330. brijoux
  54331. organocobalt
  54332. catalyzed
  54333. synthe
  54334. review
  54335. barber
  54336. nakatani
  54337. mansfield
  54338. photosynthetic
  54339. review
  54340. bardin
  54341. yagupolskii
  54342. xenon
  54343. difluoride
  54344. review
  54345. baretta
  54346. waegell
  54347. favorskii
  54348. rearrangement
  54349. mechani
  54350. review
  54351. barkash
  54352. nonclassical
  54353. carbocations
  54354. 1984116
  54355. topic
  54356. review
  54357. barker
  54358. diethienylalkanes
  54359. their
  54360. derivati
  54361. review
  54362. barlin
  54363. gordon
  54364. pyrazines
  54365. chemistry
  54366. heterocy
  54367. review
  54368. barluenga
  54369. aznar
  54370. fernando
  54371. fustero
  54372. santos
  54373. tomas
  54374. review
  54375. barluenga
  54376. palacios
  54377. francisco
  54378. synthesis
  54379. review
  54380. barluenga
  54381. preparation
  54382. applications
  54383. review
  54384. barone
  54385. guido
  54386. giancola
  54387. concetta
  54388. peptide
  54389. peptide
  54390. review
  54391. barrau
  54392. jacques
  54393. escudie
  54394. satge
  54395. jacques
  54396. multiply
  54397. review
  54398. barreto
  54399. bergter
  54400. corin
  54401. structural
  54402. chemistry
  54403. review
  54404. barrett
  54405. anthony
  54406. sturgess
  54407. michael
  54408. applications
  54409. review
  54410. barrow
  54411. biosynthesis
  54412. marine
  54413. metabolites
  54414. marin
  54415. review
  54416. bartlett
  54417. olefin
  54418. cyclization
  54419. processes
  54420. review
  54421. bartmann
  54422. prostacyclin
  54423. synthetic
  54424. analog
  54425. review
  54426. bartmann
  54427. trost
  54428. selectivity
  54429. review
  54430. bartoli
  54431. conjugate
  54432. addition
  54433. alkyl
  54434. grignard
  54435. review
  54436. barton
  54437. derek
  54438. quiclet
  54439. samadi
  54440. review
  54441. barton
  54442. derek
  54443. invention
  54444. chemical
  54445. reaction
  54446. review
  54447. barton
  54448. reactive
  54449. intermediates
  54450. organosilicon
  54451. review
  54452. baschang
  54453. muramyl
  54454. peptides
  54455. lipopeptides
  54456. studie
  54457. review
  54458. bassindale
  54459. third
  54460. dimension
  54461. organic
  54462. chemlst
  54463. review
  54464. bates
  54465. carbanion
  54466. chemistry
  54467. springer
  54468. review
  54469. baudler
  54470. chain
  54471. phosphorus
  54472. compounds
  54473. analo
  54474. review
  54475. bauld
  54476. nathan
  54477. cation
  54478. radical
  54479. cycloadditions
  54480. review
  54481. snieckus
  54482. directed
  54483. lithiation
  54484. aromatic
  54485. review
  54486. zajdel
  54487. reitz
  54488. metalation
  54489. electrop
  54490. review
  54491. becher
  54492. stidsen
  54493. carsten
  54494. recent
  54495. developments
  54496. review
  54497. becker
  54498. haddad
  54499. nizar
  54500. applications
  54501. intramolecu
  54502. review
  54503. becker
  54504. dieter
  54505. excited
  54506. state
  54507. reactivity
  54508. review
  54509. becker
  54510. synthesis
  54511. stilbenes
  54512. synthesi
  54513. review
  54514. beets
  54515. stimulant
  54516. structure
  54517. fragrance
  54518. review
  54519. behrens
  54520. transformations
  54521. epoxy
  54522. alcohol
  54523. review
  54524. belen'kii
  54525. literature
  54526. heterocyclic
  54527. chemis
  54528. review
  54529. belen'kii
  54530. editor
  54531. chemistry
  54532. organosulfur
  54533. review
  54534. beletskaya
  54535. makhon'kov
  54536. oxidation
  54537. alkyl
  54538. review
  54539. belson
  54540. strachan
  54541. preparation
  54542. properties
  54543. review
  54544. benedetti
  54545. structure
  54546. conformation
  54547. peptides
  54548. review
  54549. benner
  54550. steven
  54551. glasfeld
  54552. arthur
  54553. piccirilli
  54554. joseph
  54555. review
  54556. bennett
  54557. martin
  54558. schwemlein
  54559. heinz
  54560. metal
  54561. complexes
  54562. review
  54563. bennett
  54564. martin
  54565. stabilization
  54566. reactivity
  54567. review
  54568. benninga
  54569. history
  54570. lactic
  54571. making
  54572. chapte
  54573. review
  54574. benoiton
  54575. quantitation
  54576. sequence
  54577. dependence
  54578. review
  54579. benson
  54580. nitrogen
  54581. compounds
  54582. wiley
  54583. lnters
  54584. review
  54585. bentley
  54586. william
  54587. llewellyn
  54588. gareth
  54589. scales
  54590. review
  54591. bentrude
  54592. phosphoranyl
  54593. radicals
  54594. reactive
  54595. interme
  54596. review
  54597. bentrude
  54598. phosphoranyl
  54599. radicals
  54600. their
  54601. structure
  54602. review
  54603. berdy
  54604. handbook
  54605. antibiotic
  54606. compounds
  54607. volume
  54608. review
  54609. sandstrom
  54610. steric
  54611. dynamic
  54612. stereoche
  54613. review
  54614. bergbretter
  54615. newcomb
  54616. alkylation
  54617. imine
  54618. review
  54619. bergeron
  54620. synthesis
  54621. solution
  54622. structure
  54623. review
  54624. bergman
  54625. quinazolinocarboline
  54626. alkaloids
  54627. review
  54628. bergman
  54629. pelcman
  54630. benjamina
  54631. synthesis
  54632. carbazol
  54633. review
  54634. bergquist
  54635. wells
  54636. chemotaxonomy
  54637. porife
  54638. review
  54639. bergstrom
  54640. organometallic
  54641. intermediates
  54642. review
  54643. bergstrom
  54644. swartling
  54645. fluorine
  54646. substituted
  54647. review
  54648. bernal
  54649. stereochemistry
  54650. organometallic
  54651. review
  54652. bernardi
  54653. fernando
  54654. olivucci
  54655. massimo
  54656. michael
  54657. review
  54658. bernasconi
  54659. claude
  54660. nucleophilic
  54661. addition
  54662. olefin
  54663. review
  54664. berson
  54665. jerome
  54666. reaction
  54667. symmetry
  54668. criteriain
  54669. review
  54670. bestmann
  54671. schmid
  54672. kisielowski
  54673. synthesis
  54674. review
  54675. bhatt
  54676. kulkarni
  54677. cleavage
  54678. ethers
  54679. review
  54680. bickelhaupt
  54681. friedrich
  54682. willem
  54683. bridged
  54684. review
  54685. bickelhaupt
  54686. friedrich
  54687. trends
  54688. dimetallic
  54689. review
  54690. bickelhaupt
  54691. friedrich
  54692. small
  54693. cyclophanes
  54694. review
  54695. bicyclo
  54696. 4.2.1
  54697. nonane
  54698. skeleton
  54699. conformational
  54700. analys
  54701. review
  54702. biehl
  54703. edward
  54704. khanapure
  54705. subhash
  54706. synthesis
  54707. review
  54708. biellmann
  54709. ducep
  54710. allylic
  54711. benzylic
  54712. carban
  54713. review
  54714. biermann
  54715. christopher
  54716. hydrolysis
  54717. other
  54718. cleavag
  54719. review
  54720. billington
  54721. david
  54722. recent
  54723. developments
  54724. synth
  54725. review
  54726. billups
  54727. haley
  54728. michael
  54729. bicyclo
  54730. review
  54731. billups
  54732. rodin
  54733. wayne
  54734. haley
  54735. michael
  54736. cycloprop
  54737. review
  54738. biloen
  54739. sachtler
  54740. mechanism
  54741. hydrocarbon
  54742. review
  54743. bishop
  54744. dance
  54745. types
  54746. helical
  54747. canal
  54748. inclu
  54749. review
  54750. black
  54751. recent
  54752. applications
  54753. homogeneous
  54754. cataly
  54755. review
  54756. black
  54757. preparation
  54758. reactions
  54759. diazomet
  54760. review
  54761. black
  54762. howard
  54763. recent
  54764. progress
  54765. control
  54766. review
  54767. blackburn
  54768. brent
  54769. davies
  54770. stephen
  54771. sutton
  54772. kevin
  54773. review
  54774. blaney
  54775. structure
  54776. activity
  54777. relationships
  54778. review
  54779. blasko
  54780. dabor
  54781. spirobenzylisoquinol
  54782. related
  54783. alkal
  54784. review
  54785. blasko
  54786. gabor
  54787. cordell
  54788. geoffrey
  54789. isolation
  54790. structure
  54791. review
  54792. blechert
  54793. hetero
  54794. rearrangement
  54795. organic
  54796. review
  54797. blechert
  54798. siegfried
  54799. guenard
  54800. daniel
  54801. taxus
  54802. alkaloids
  54803. review
  54804. blenderman
  54805. joullie
  54806. synthetic
  54807. approaches
  54808. review
  54809. blinka
  54810. helmer
  54811. polarization
  54812. transfer
  54813. review
  54814. block
  54815. olefin
  54816. synthesis
  54817. deoxygenation
  54818. vicina
  54819. review
  54820. block
  54821. synthesis
  54822. chemistry
  54823. heteroato
  54824. review
  54825. blondet
  54826. morin
  54827. synthesis
  54828. reactivity
  54829. review
  54830. bloxsidge
  54831. elvidge
  54832. practical
  54833. aspects
  54834. review
  54835. blystone
  54836. sheri
  54837. synthetic
  54838. applications
  54839. enantios
  54840. review
  54841. black
  54842. preparation
  54843. reactions
  54844. diazomet@
  54845. review
  54846. boche
  54847. structure
  54848. lithium
  54849. compounds
  54850. sulfo@
  54851. review
  54852. boger
  54853. patel
  54854. recent
  54855. applications
  54856. invers@
  54857. review
  54858. vernon
  54859. interactions
  54860. review
  54861. bristow
  54862. reagents
  54863. organic
  54864. synthesis
  54865. 1984@
  54866. review
  54867. brownbridge
  54868. silyl
  54869. ethers
  54870. synthesis
  54871. review
  54872. buchwald
  54873. stephen
  54874. fisher
  54875. richard
  54876. zirconocene
  54877. review
  54878. burnell
  54879. apsimon
  54880. echinoderm
  54881. saponins
  54882. marine
  54883. review
  54884. capozzi
  54885. francesco
  54886. capozzi
  54887. giuseppe
  54888. menichetti
  54889. stefa@
  54890. review
  54891. catellani
  54892. marta
  54893. chiusoli
  54894. paolo
  54895. costa
  54896. mirco
  54897. review
  54898. charton
  54899. marvin
  54900. quantitative
  54901. description
  54902. amin@
  54903. review
  54904. childs
  54905. circumambulatory
  54906. rearrangements
  54907. review
  54908. chukovskaya
  54909. synthesis
  54910. substituted
  54911. cyclo@
  54912. review
  54913. cohen
  54914. theodore
  54915. bhupathy
  54916. mahadevan
  54917. organoalkali
  54918. comp@
  54919. review
  54920. boche
  54921. structure
  54922. lithium
  54923. compounds
  54924. sulfo
  54925. review
  54926. boche
  54927. walborsky
  54928. cyclopropane
  54929. derived
  54930. reactive
  54931. review
  54932. boche
  54933. gernot
  54934. rearrangements
  54935. carbanions
  54936. review
  54937. organosilicon
  54938. radical
  54939. cations
  54940. review
  54941. fundamentals
  54942. silicon
  54943. chemistry
  54944. molecul
  54945. review
  54946. novel
  54947. group
  54948. element
  54949. cyclic
  54950. molecules
  54951. review
  54952. pedersen
  54953. carbon
  54954. nuclear
  54955. magnetic
  54956. resona
  54957. review
  54958. pedersen
  54959. pedersen
  54960. carbon
  54961. nuclear
  54962. review
  54963. bodanszky
  54964. martinez
  54965. reactions
  54966. peptide
  54967. review
  54968. boeckman
  54969. robert
  54970. walters
  54971. michael
  54972. scope
  54973. review
  54974. boekelheide
  54975. syntheses
  54976. properties
  54977. review
  54978. boelens
  54979. acyclic
  54980. monoterpene
  54981. alcohols
  54982. review
  54983. bogan
  54984. phase
  54985. dioxetane
  54986. chemiluminescences
  54987. review
  54988. bogatskii
  54989. zhilina
  54990. sterically
  54991. hindered
  54992. porph
  54993. review
  54994. boger
  54995. diels
  54996. alder
  54997. reactions
  54998. azadienes
  54999. review
  55000. boger
  55001. patel
  55002. recent
  55003. applications
  55004. invers
  55005. review
  55006. boger
  55007. brotherton
  55008. pleiss
  55009. christine
  55010. thermal
  55011. review
  55012. bogulavskaya
  55013. chuvatkin
  55014. halogen
  55015. fluorides
  55016. review
  55017. boguslavskaya
  55018. kartashov
  55019. chuvatkin
  55020. selec
  55021. review
  55022. bonner
  55023. william
  55024. origins
  55025. chiral
  55026. homogeneity
  55027. review
  55028. borden
  55029. diradicals
  55030. reactive
  55031. intermediates
  55032. review
  55033. borden
  55034. diradicals
  55035. wiley
  55036. jersey
  55037. review
  55038. borden
  55039. weston
  55040. thatcher
  55041. pyramidalized
  55042. alkenes
  55043. review
  55044. borman
  55045. linda
  55046. kuehne
  55047. martin
  55048. functional
  55049. review
  55050. borovkov
  55051. evstigneeva
  55052. strekova
  55053. filippovi
  55054. review
  55055. bortolini
  55056. furia
  55057. fulvio
  55058. licini
  55059. giulia
  55060. modena
  55061. review
  55062. bosch
  55063. bennasar
  55064. elaboration
  55065. ethylidene
  55066. review
  55067. bowman
  55068. reactivity
  55069. substituted
  55070. aliphatic
  55071. review
  55072. consequences
  55073. interactio
  55074. review
  55075. interactions
  55076. review
  55077. vernon
  55078. interactions
  55079. review
  55080. theoretical
  55081. physicochemical
  55082. studies
  55083. review
  55084. boykin
  55085. david
  55086. baumstark
  55087. alfons
  55088. oxygen
  55089. review
  55090. bradley
  55091. chemistry
  55092. carbidocarbonyl
  55093. cluste
  55094. review
  55095. braekman
  55096. daloze
  55097. moussiaux
  55098. stoller
  55099. deneubo
  55100. review
  55101. bragin
  55102. catalytic
  55103. cyclo
  55104. oligomerisation
  55105. reaction
  55106. review
  55107. brandsma
  55108. preparative
  55109. acetylenic
  55110. chemistry
  55111. review
  55112. braunstein
  55113. pierre
  55114. nobel
  55115. dominique
  55116. transitionmetal
  55117. review
  55118. bregadze
  55119. kampel
  55120. usyatinskii
  55121. godovikov
  55122. review
  55123. bremner
  55124. browne
  55125. gunawardana
  55126. oxaza
  55127. review
  55128. breslow
  55129. ronald
  55130. chmielewski
  55131. foley
  55132. diane
  55133. johnson
  55134. review
  55135. breslow
  55136. ronald
  55137. enzyme
  55138. mimics
  55139. review
  55140. breuer
  55141. aurich
  55142. guenther
  55143. nielsen
  55144. arnold
  55145. review
  55146. silicon
  55147. nuclear
  55148. magnetic
  55149. resonance
  55150. review
  55151. bringmann
  55152. gerhard
  55153. welter
  55154. rainer
  55155. wenieb
  55156. review
  55157. bristow
  55158. reagents
  55159. organic
  55160. synthesis
  55161. review
  55162. broadbent
  55163. carbon
  55164. nuclear
  55165. magnetic
  55166. review
  55167. brook
  55168. silene
  55169. chemistry
  55170. silicon
  55171. compounds
  55172. review
  55173. brossi
  55174. alkaloids
  55175. volume
  55176. academic
  55177. press
  55178. review
  55179. brossi
  55180. arnold
  55181. research
  55182. bioactive
  55183. natural
  55184. product
  55185. review
  55186. brown
  55187. jadhav
  55188. asymmetric
  55189. hydroboration
  55190. volum
  55191. review
  55192. brown
  55193. energy
  55194. transition
  55195. states
  55196. review
  55197. brown
  55198. herbert
  55199. asymmetric
  55200. synthesis
  55201. review
  55202. brown
  55203. herbert
  55204. ramachandran
  55205. veeraraghavan
  55206. review
  55207. brown
  55208. asymmetric
  55209. homogeneous
  55210. catalysis
  55211. review
  55212. brown
  55213. catalytic
  55214. kinetic
  55215. resolution
  55216. review
  55217. brown
  55218. literature
  55219. review
  55220. ester
  55221. enolate
  55222. review
  55223. brown
  55224. thermal
  55225. rearrangements
  55226. alkynes
  55227. under
  55228. review
  55229. brown
  55230. roger
  55231. flash
  55232. pyrolytic
  55233. reactions
  55234. usefu
  55235. review
  55236. brownbridge
  55237. silyl
  55238. ethers
  55239. synthesis
  55240. review
  55241. brownbridge
  55242. silyl
  55243. ethers
  55244. synthesis
  55245. review
  55246. bruce
  55247. swincer
  55248. vinylidene
  55249. propadienylide
  55250. review
  55251. bruce
  55252. michael
  55253. carbenes
  55254. carbides
  55255. carbon
  55256. review
  55257. bruce
  55258. michael
  55259. organometallic
  55260. chemistry
  55261. vinylid
  55262. review
  55263. bruice
  55264. thomas
  55265. mechanisms
  55266. oxygen
  55267. transfer
  55268. review
  55269. waegall
  55270. synthetic
  55271. applications
  55272. reactiv
  55273. review
  55274. brunet
  55275. tetracarbonylhydrido
  55276. versatile
  55277. review
  55278. brunner
  55279. henri
  55280. enantioselective
  55281. synthesis
  55282. organic
  55283. review
  55284. brunner
  55285. henri
  55286. right
  55287. question
  55288. review
  55289. bubnov
  55290. allylic
  55291. bisboranes
  55292. review
  55293. buchachenko
  55294. organic
  55295. molecular
  55296. ferromagnetic
  55297. review
  55298. buchanan
  55299. dakin
  55300. reaction
  55301. 198817
  55302. review
  55303. buchanan
  55304. gerald
  55305. applications
  55306. nitrogen
  55307. review
  55308. buchanan
  55309. nucleoside
  55310. antibiotics
  55311. review
  55312. buchel
  55313. chemistry
  55314. pesticides
  55315. wiley
  55316. intersc
  55317. review
  55318. buchwald
  55319. stephen
  55320. fisher
  55321. richard
  55322. zirconocene
  55323. review
  55324. spectrophysics
  55325. photochemistry
  55326. review
  55327. spectrophysics
  55328. photochemistry
  55329. ofthe
  55330. review
  55331. azafluoranthene
  55332. tropoloisoquinoline
  55333. review
  55334. bucke
  55335. rastoll
  55336. synthesizing
  55337. sugars
  55338. enzymes
  55339. review
  55340. buckus
  55341. debenzhydrylation
  55342. transbenzhydryla
  55343. review
  55344. charles
  55345. ealick
  55346. steven
  55347. crystallographic
  55348. review
  55349. bumgardner
  55350. whangbo
  55351. secondary
  55352. orbital
  55353. effect
  55354. review
  55355. bundle
  55356. david
  55357. synthesis
  55358. oligosaccharides
  55359. relate
  55360. review
  55361. bunds
  55362. preparation
  55363. properties
  55364. industrial
  55365. review
  55366. burgess
  55367. kevin
  55368. buckminsterfullerene
  55369. great
  55370. balls
  55371. review
  55372. burgoyne
  55373. william
  55374. dison
  55375. casey
  55376. jeremiah
  55377. review
  55378. burkert
  55379. allinger
  55380. molecular
  55381. mechanics
  55382. american
  55383. review
  55384. burkhardt
  55385. elizabeth
  55386. doney
  55387. jeffrey
  55388. slough
  55389. review
  55390. burmakov
  55391. kunshenko
  55392. alekseeva
  55393. yagupolski
  55394. review
  55395. burnell
  55396. apsimon
  55397. echinoderm
  55398. saponins
  55399. marine
  55400. review
  55401. bursian
  55402. kogan
  55403. catalytic
  55404. conversion
  55405. paraf
  55406. review
  55407. burton
  55408. stereospecific
  55409. preparation
  55410. reactivity
  55411. review
  55412. burwell
  55413. robert
  55414. mechanisms
  55415. heterogeneous
  55416. review
  55417. busby
  55418. reginald
  55419. thiadiazines
  55420. adjacent
  55421. sulfur
  55422. review
  55423. butler
  55424. cyclopolymerization
  55425. cyclocopolymeriz
  55426. review
  55427. butler
  55428. comparative
  55429. reactions
  55430. nitrogen
  55431. compou
  55432. review
  55433. bradsher
  55434. formation
  55435. review
  55436. ghosh
  55437. bandyopadhyay
  55438. maiti
  55439. heterocycles
  55440. review
  55441. kashima
  55442. tajima
  55443. synth
  55444. review
  55445. buchecker
  55446. sauvage
  55447. interlock
  55448. review
  55449. cacchi
  55450. sandro
  55451. palladium
  55452. catalyzed
  55453. hydroarylatio
  55454. review
  55455. cainelli
  55456. gianfranco
  55457. panunzio
  55458. mauro
  55459. andreoli
  55460. patrizi
  55461. review
  55462. caminade
  55463. marie
  55464. majoral
  55465. pierre
  55466. routes
  55467. review
  55468. campaigne
  55469. adventures
  55470. organic
  55471. sulfur
  55472. chemistry
  55473. review
  55474. capozzi
  55475. francesco
  55476. capozzi
  55477. giuseppe
  55478. menichetti
  55479. stefa
  55480. review
  55481. capraro
  55482. brossi
  55483. tropolonic
  55484. colchicum
  55485. alkaloids
  55486. review
  55487. capraro
  55488. george
  55489. schneider
  55490. peter
  55491. synth
  55492. review
  55493. cardillo
  55494. giuliana
  55495. orena
  55496. mario
  55497. sandri
  55498. sergio
  55499. stereoc
  55500. review
  55501. cardillo
  55502. giuliana
  55503. orena
  55504. mario
  55505. stereocontrolled
  55506. review
  55507. carey
  55508. francis
  55509. sundberg
  55510. richard
  55511. advanced
  55512. organic
  55513. review
  55514. carmona
  55515. ernesto
  55516. campora
  55517. munoz
  55518. miguel
  55519. paneque
  55520. review
  55521. carpenter
  55522. determination
  55523. organic
  55524. reaction
  55525. review
  55526. carruthers
  55527. cycloaddition
  55528. reactions
  55529. organic
  55530. review
  55531. casey
  55532. metal
  55533. carbene
  55534. complexes
  55535. reactive
  55536. review
  55537. casey
  55538. leonard
  55539. procter
  55540. advanced
  55541. practic
  55542. review
  55543. caspar
  55544. silylenes
  55545. reactive
  55546. intermediates
  55547. review
  55548. castedo
  55549. dominguez
  55550. dibenzazonine
  55551. alkaloids
  55552. review
  55553. castedo
  55554. gabriel
  55555. phenanthrene
  55556. alkaloids
  55557. review
  55558. castro
  55559. replacement
  55560. alcoholic
  55561. hydroxyl
  55562. groups
  55563. review
  55564. catellani
  55565. marta
  55566. chiusoli
  55567. paolo
  55568. costa
  55569. mirco
  55570. review
  55571. caton
  55572. recent
  55573. syntheses
  55574. prostaglandins
  55575. review
  55576. catsoulacos
  55577. camoutsis
  55578. steroidal
  55579. thiazoles
  55580. isoth
  55581. review
  55582. caubere
  55583. complex
  55584. reducing
  55585. agents
  55586. cra's
  55587. versatile
  55588. review
  55589. caubere
  55590. aggregative
  55591. activation
  55592. helpful
  55593. conce
  55594. review
  55595. leboeuf
  55596. cassels
  55597. alkaloids
  55598. guattet
  55599. review
  55600. cerveau
  55601. chuit
  55602. corriu
  55603. reactivity
  55604. review
  55605. cerveny
  55606. ruzicka
  55607. solvent
  55608. structure
  55609. effects
  55610. review
  55611. recent
  55612. developments
  55613. synthesis
  55614. review
  55615. chamberlin
  55616. richard
  55617. bloom
  55618. steven
  55619. lithioalkenes
  55620. review
  55621. chanon
  55622. rajzmann
  55623. chanon
  55624. electron
  55625. review
  55626. chanon
  55627. electron
  55628. transfer
  55629. catalysis
  55630. review
  55631. chapdelaine
  55632. hulce
  55633. martin
  55634. tandem
  55635. vicinal
  55636. review
  55637. charpentier
  55638. morize
  55639. micheline
  55640. bonnet
  55641. delpon
  55642. daniele
  55643. review
  55644. charton
  55645. electrical
  55646. effect
  55647. substituent
  55648. constants
  55649. review
  55650. charton
  55651. marvin
  55652. quantitative
  55653. description
  55654. review
  55655. charushin
  55656. alekseev
  55657. chupakhin
  55658. review
  55659. charushin
  55660. chupakhin
  55661. review
  55662. chaussard
  55663. jacques
  55664. folest
  55665. claude
  55666. nedelec
  55667. review
  55668. tench
  55669. characterization
  55670. reactivity
  55671. review
  55672. cheikh
  55673. chaabouni
  55674. laurent
  55675. mison
  55676. nafti
  55677. review
  55678. chemical
  55679. biochemical
  55680. studies
  55681. reactivities
  55682. review
  55683. chemistry
  55684. polyhedral
  55685. boron
  55686. halides
  55687. review
  55688. chemyshev
  55689. komalenkova
  55690. generation
  55691. reacti
  55692. review
  55693. general
  55694. aspects
  55695. optimization
  55696. review
  55697. rongsi
  55698. cyvin
  55699. cyvin
  55700. brunvoll
  55701. klein
  55702. review
  55703. cheng
  55704. friedlander
  55705. synthesis
  55706. review
  55707. cherkasov
  55708. ovchinnikov
  55709. pudovik
  55710. pudovik
  55711. review
  55712. chernyshev
  55713. komalenkova
  55714. thermal
  55715. review
  55716. cherry
  55717. newall
  55718. clavulanic
  55719. chemistry
  55720. review
  55721. childs
  55722. circumambulatory
  55723. rearrangements
  55724. review
  55725. childs
  55726. homotropylium
  55727. homoaromaticit
  55728. review
  55729. chilton
  55730. secondary
  55731. amino
  55732. acids
  55733. mushrooms
  55734. review
  55735. chimiak
  55736. andrzej
  55737. milewska
  55738. mariaj
  55739. hydroxyaminoacids
  55740. review
  55741. chimirri
  55742. grasso
  55743. silvana
  55744. romeo
  55745. giovanni
  55746. zappala
  55747. review
  55748. chini
  55749. compounds
  55750. metal
  55751. bonds
  55752. cluster
  55753. review
  55754. chisholm
  55755. malcolm
  55756. carbon
  55757. carbon
  55758. carbon
  55759. hydroge
  55760. review
  55761. chisholm
  55762. malcolm
  55763. clark
  55764. david
  55765. hampden
  55766. smith
  55767. review
  55768. chiusoli
  55769. paolo
  55770. costa
  55771. micro
  55772. pelizzi
  55773. corrado
  55774. review
  55775. chojnowski
  55776. julian
  55777. stimczyk
  55778. wlodzmmierz
  55779. dissociative
  55780. review
  55781. substituted
  55782. sulfo
  55783. review
  55784. christensen
  55785. tienam
  55786. natural
  55787. product
  55788. review
  55789. christopherson
  55790. marine
  55791. indoles
  55792. marine
  55793. natural
  55794. review
  55795. studies
  55796. diterpene
  55797. alkaloids
  55798. review
  55799. chukovskaya
  55800. freidlina
  55801. kuz'mina
  55802. reducti
  55803. review
  55804. chukovskaya
  55805. synthesis
  55806. substituted
  55807. cyclo
  55808. review
  55809. chupakhin
  55810. charushin
  55811. review
  55812. churms
  55813. shirley
  55814. handbook
  55815. chromatography
  55816. review
  55817. chvalovsky
  55818. bellama
  55819. carbon
  55820. functional
  55821. review
  55822. ciganek
  55823. intramolecular
  55824. diels
  55825. alder
  55826. reaction
  55827. review
  55828. cilente
  55829. electronic
  55830. excitation
  55831. biological
  55832. review
  55833. cioslowski
  55834. jerzy
  55835. scaling
  55836. properties
  55837. topological
  55838. review
  55839. cirrincione
  55840. girolamo
  55841. almerico
  55842. maria
  55843. aiello
  55844. review
  55845. claesson
  55846. biologically
  55847. active
  55848. allenes
  55849. chemistr
  55850. review
  55851. claesson
  55852. olsson
  55853. allenic
  55854. intermediates
  55855. review
  55856. claret
  55857. osborne
  55858. alkylquinolines
  55859. arylquin
  55860. review
  55861. clark
  55862. repke
  55863. leimgruber
  55864. batcho
  55865. indole
  55866. review
  55867. clarke
  55868. ronald
  55869. coates
  55870. lincoln
  55871. stephen
  55872. review
  55873. clouthier
  55874. dennis
  55875. moule
  55876. david
  55877. periodic
  55878. group
  55879. review
  55880. cocagne
  55881. elguero
  55882. gallo
  55883. present
  55884. review
  55885. cohen
  55886. theodore
  55887. bhupathy
  55888. mahadevan
  55889. organoalkali
  55890. review
  55891. collin
  55892. photochemistry
  55893. simple
  55894. olefins
  55895. chemi
  55896. review
  55897. collin
  55898. jacqueline
  55899. double
  55900. carbonylation
  55901. reactions
  55902. review
  55903. collins
  55904. mammalian
  55905. alkaloids
  55906. alkaloids
  55907. volum
  55908. review
  55909. colomer
  55910. ernest
  55911. corriu
  55912. robert
  55913. lheureux
  55914. review
  55915. colquhoun
  55916. holton
  55917. thompson
  55918. twigg
  55919. review
  55920. colthup
  55921. norman
  55922. lawrence
  55923. wiberley
  55924. stephen
  55925. review
  55926. comins
  55927. daniel
  55928. o'connor
  55929. regioselective
  55930. substi
  55931. review
  55932. confalone
  55933. edward
  55934. nitrone
  55935. olefi
  55936. review
  55937. connelly
  55938. geiger
  55939. electron
  55940. transfer
  55941. react
  55942. review
  55943. consiglio
  55944. asymmetric
  55945. hydroformylation
  55946. review
  55947. consiglio
  55948. giambattista
  55949. waymouth
  55950. robert
  55951. enantiosel
  55952. review
  55953. controlling
  55954. electrochemical
  55955. catalysis
  55956. surfacta
  55957. review
  55958. cooley
  55959. elvain
  55960. amine
  55961. dealkylations
  55962. review
  55963. cooper
  55964. ginos
  55965. meister
  55966. synthesis
  55967. review
  55968. cooper
  55969. ginos
  55970. meister
  55971. synthesis
  55972. review
  55973. cooper
  55974. david
  55975. gerratt
  55976. joseph
  55977. raimondi
  55978. mario
  55979. review
  55980. cooper
  55981. koppel
  55982. chemistry
  55983. penicillin
  55984. review
  55985. cooper
  55986. stephen
  55987. supertripodal
  55988. ligands
  55989. 199062
  55990. review
  55991. coote
  55992. steven
  55993. davies
  55994. stephen
  55995. goodfellow
  55996. craig
  55997. review
  55998. corey
  55999. cheng
  56000. logic
  56001. chemical
  56002. synth
  56003. review
  56004. corey
  56005. enantioselective
  56006. routes
  56007. biological
  56008. review
  56009. corey
  56010. retrosynthetic
  56011. thinking
  56012. essentials
  56013. review
  56014. corey
  56015. corey
  56016. gaspar
  56017. silicon
  56018. chemistr
  56019. review
  56020. corey
  56021. joyce
  56022. dehydrogenative
  56023. coupling
  56024. reactions
  56025. review
  56026. corriu
  56027. guerin
  56028. nucleophilic
  56029. displacement
  56030. review
  56031. corriu
  56032. aspects
  56033. reactivity
  56034. hyperval
  56035. review
  56036. covering
  56037. induced
  56038. nucleophilic
  56039. substitution
  56040. review
  56041. coyle
  56042. electron
  56043. transfer
  56044. photochemistry
  56045. review
  56046. crabb
  56047. trevor
  56048. jackson
  56049. david
  56050. patel
  56051. asmita
  56052. saturat
  56053. review
  56054. cooper
  56055. ginos
  56056. meister
  56057. synthesis
  56058. review
  56059. craik
  56060. brownlee
  56061. substituent
  56062. effects
  56063. chemi@
  56064. review
  56065. crowe
  56066. william
  56067. schreiber
  56068. stuart
  56069. hybridiza@
  56070. review
  56071. massy
  56072. synthesis
  56073. review
  56074. thioalkylat@
  56075. review
  56076. dannenberg
  56077. molecular
  56078. orbital
  56079. modeling
  56080. review
  56081. davies
  56082. stephen
  56083. brown
  56084. pratt
  56085. fleet
  56086. review
  56087. recent
  56088. advances
  56089. furan
  56090. chemistry
  56091. review
  56092. yadav
  56093. narula
  56094. handbook
  56095. terpenoids@
  56096. review
  56097. dixneuf
  56098. pierre
  56099. activation
  56100. alkynes
  56101. rutheni
  56102. review
  56103. carbene
  56104. complexes
  56105. organic
  56106. synthesis
  56107. review
  56108. duran
  56109. singlet
  56110. oxygen
  56111. biological
  56112. processes
  56113. chem@
  56114. review
  56115. ebetino
  56116. frank
  56117. degenhardt
  56118. charles
  56119. jamieson
  56120. laura@
  56121. review
  56122. elnagdi
  56123. elfahham
  56124. elgemeie
  56125. utility
  56126. review
  56127. erdik
  56128. ender
  56129. mehmet
  56130. electrophilic
  56131. amination
  56132. review
  56133. craik
  56134. brownlee
  56135. substituent
  56136. effects
  56137. chemi
  56138. review
  56139. craine
  56140. leslie
  56141. raban
  56142. morton
  56143. chemistry
  56144. sulfena
  56145. review
  56146. cyclophanes
  56147. personal
  56148. account
  56149. cyclophanes
  56150. review
  56151. crandall
  56152. apparu
  56153. promoted
  56154. isomerizations
  56155. review
  56156. crass
  56157. katritzky
  56158. conformational
  56159. equilibria
  56160. review
  56161. creary
  56162. xavier
  56163. hopkinson
  56164. edward
  56165. review
  56166. cremer
  56167. dieter
  56168. aromaticity
  56169. review
  56170. crich
  56171. david
  56172. quintero
  56173. leticia
  56174. radical
  56175. chemistry
  56176. review
  56177. criddle
  56178. ellis
  56179. spectral
  56180. chemical
  56181. charact
  56182. review
  56183. criller
  56184. nazran
  56185. scaiano
  56186. flash
  56187. photolysis
  56188. review
  56189. crippa
  56190. horak
  56191. protn
  56192. svoronos
  56193. wolfram
  56194. chemi
  56195. review
  56196. cristol
  56197. bindel
  56198. photosolvolyses
  56199. attendant
  56200. review
  56201. crockett
  56202. chemical
  56203. synthesis
  56204. review
  56205. croft
  56206. bartsch
  56207. synthesis
  56208. chemically
  56209. modif
  56210. review
  56211. crombie
  56212. crombie
  56213. whiting
  56214. alkaloids
  56215. review
  56216. crowe
  56217. william
  56218. schreiber
  56219. stuart
  56220. hybridiza
  56221. review
  56222. glaenzer
  56223. brigitte
  56224. baker's
  56225. yeast
  56226. mediate
  56227. review
  56228. glanzer
  56229. brigitte
  56230. spectroscopy
  56231. review
  56232. cunico
  56233. synthetic
  56234. aspects
  56235. acylsilane
  56236. chemistr
  56237. review
  56238. robert
  56239. smalley
  56240. richard
  56241. probing
  56242. review
  56243. curran
  56244. cycloaddition
  56245. approach
  56246. alpha
  56247. review
  56248. curran
  56249. dennis
  56250. tandem
  56251. radical
  56252. cyclizations
  56253. gener
  56254. review
  56255. curriu
  56256. guerin
  56257. moreau
  56258. stereochemistry
  56259. review
  56260. cybulski
  56261. wrobel
  56262. nuphar
  56263. alkaloids
  56264. alkaloid
  56265. review
  56266. craig
  56267. stereochemical
  56268. review
  56269. crich
  56270. aldrichimica
  56271. thiohyd
  56272. review
  56273. crich
  56274. aldrichimica
  56275. acylthiohydr
  56276. review
  56277. perrin
  56278. armarego
  56279. pergamon
  56280. press
  56281. review
  56282. ginsburg
  56283. propellanes
  56284. review
  56285. barton
  56286. bismu
  56287. review
  56288. massy
  56289. synthesis
  56290. review
  56291. thioalkylat
  56292. review
  56293. lloyd
  56294. gosney
  56295. ormiston
  56296. review
  56297. goodall
  56298. norton
  56299. review
  56300. matteson
  56301. synthesis
  56302. chiral
  56303. review
  56304. ribbons
  56305. fluorine
  56306. biotr
  56307. review
  56308. roberts
  56309. williams
  56310. tetrahedron
  56311. review
  56312. daboun
  56313. abdou
  56314. recent
  56315. developments
  56316. review
  56317. dahlhoff
  56318. koster
  56319. ethylboron
  56320. assiste
  56321. review
  56322. dahne
  56323. siegfried
  56324. hoffmann
  56325. katrin
  56326. energy
  56327. relatio
  56328. review
  56329. nagao
  56330. yoshimitsu
  56331. fujita
  56332. eiichi
  56333. recent
  56334. review
  56335. dallas
  56336. ruane
  56337. wilson
  56338. recent
  56339. review
  56340. daloutin
  56341. pashkevich
  56342. postovskii
  56343. fluorin
  56344. review
  56345. alkaloids
  56346. neotropical
  56347. poison
  56348. frogs
  56349. review
  56350. danishefsky
  56351. samuel
  56352. cycloaddition
  56353. cyclocondensat
  56354. review
  56355. danishefsky
  56356. samuel
  56357. simoneau
  56358. bruno
  56359. synthetic
  56360. studi
  56361. review
  56362. dannenberg
  56363. molecular
  56364. orbital
  56365. modeling
  56366. review
  56367. darbarwar
  56368. sundarameurthy
  56369. synthesis
  56370. coumarins
  56371. review
  56372. darensbourg
  56373. kudaroski
  56374. activation
  56375. review
  56376. darensbourg
  56377. mechanistic
  56378. pathways
  56379. ligand
  56380. review
  56381. darensbourg
  56382. marcetta
  56383. silva
  56384. review
  56385. daves
  56386. doyle
  56387. glycoside
  56388. synthesis
  56389. palladium
  56390. review
  56391. daves
  56392. doyle
  56393. hallberg
  56394. anders
  56395. additions
  56396. review
  56397. daves
  56398. doyle
  56399. palladium
  56400. mediated
  56401. arylation
  56402. review
  56403. davidson
  56404. preston
  56405. transition
  56406. organome
  56407. review
  56408. davidson
  56409. goodin
  56410. photochemistry
  56411. review
  56412. davidson
  56413. chemistry
  56414. excited
  56415. complexes
  56416. review
  56417. davies
  56418. coleman
  56419. rivett
  56420. naturally
  56421. occurring
  56422. review
  56423. davies
  56424. green
  56425. kelly
  56426. roberts
  56427. stanley
  56428. review
  56429. davies
  56430. stephen
  56431. asymmetric
  56432. synthesis
  56433. review
  56434. davies
  56435. stephen
  56436. brown
  56437. pratt
  56438. fleet
  56439. review
  56440. davies
  56441. stephen
  56442. brown
  56443. pratt
  56444. fleet
  56445. review
  56446. davies
  56447. stephen
  56448. chiral
  56449. auxiliaries
  56450. review
  56451. davies
  56452. stephen
  56453. mcnally
  56454. smallridge
  56455. andrew
  56456. review
  56457. davies
  56458. stephen
  56459. chiral
  56460. auxiliary
  56461. review
  56462. davis
  56463. jenkins
  56464. synthesis
  56465. utilization
  56466. review
  56467. davis
  56468. franklin
  56469. sheppard
  56470. aurelia
  56471. applications
  56472. review
  56473. davis
  56474. sulfur
  56475. transfer
  56476. reagents
  56477. heterocyclic
  56478. review
  56479. kimpe
  56480. schamp
  56481. reactivity
  56482. haloenamines
  56483. review
  56484. kimpe
  56485. robert
  56486. verhe
  56487. roland
  56488. chemistry
  56489. review
  56490. electrophilic
  56491. additions
  56492. unsatur
  56493. review
  56494. lucchi
  56495. ottorino
  56496. pasquato
  56497. lucia
  56498. sulfu
  56499. review
  56500. mayer
  56501. chemical
  56502. relaxation
  56503. methods
  56504. review
  56505. reuck
  56506. angus
  56507. craven
  56508. wakeham
  56509. review
  56510. dealing
  56511. chemistry
  56512. sulfines
  56513. review
  56514. recent
  56515. advances
  56516. furan
  56517. chemistry
  56518. review
  56519. recent
  56520. advances
  56521. furan
  56522. chemistry
  56523. review
  56524. expanded
  56525. systems
  56526. cyclopropenes
  56527. review
  56528. dejong
  56529. reinhoudt
  56530. stability
  56531. reactivity
  56532. review
  56533. delucchi
  56534. modena
  56535. acetylene
  56536. equivalents
  56537. cycloa
  56538. review
  56539. demuth
  56540. mikhail
  56541. developments
  56542. field
  56543. review
  56544. demuth
  56545. schaffner
  56546. tricyclo
  56547. 3.3.0.028
  56548. octan
  56549. review
  56550. denisova
  56551. dyatlovn
  56552. glyzin
  56553. natural
  56554. xanthones
  56555. review
  56556. derkach
  56557. levchenko
  56558. analogs
  56559. organic
  56560. review
  56561. descotes
  56562. gerard
  56563. synthetic
  56564. saccharide
  56565. photochemistry
  56566. review
  56567. describing
  56568. azirine
  56569. chemistry
  56570. review
  56571. deshong
  56572. lander
  56573. leginus
  56574. diekson
  56575. review
  56576. desideno
  56577. dominic
  56578. spectrometry
  56579. peptides
  56580. review
  56581. desimoni
  56582. tacconi
  56583. barco
  56584. pollini
  56585. natural
  56586. review
  56587. deslongchamps
  56588. stereoelectronic
  56589. effects
  56590. organic
  56591. review
  56592. desongchamps
  56593. concept
  56594. strategy
  56595. organic
  56596. review
  56597. yadav
  56598. narula
  56599. handbook
  56600. terpenoids
  56601. review
  56602. handbook
  56603. terpenoids
  56604. triterpenoid
  56605. review
  56606. guggultetrols
  56607. class
  56608. naturally
  56609. review
  56610. devlin
  56611. hargrave
  56612. design
  56613. synthe
  56614. review
  56615. deyrup
  56616. aziridines
  56617. chemistry
  56618. heterocyclic
  56619. review
  56620. dhingra
  56621. intramolecular
  56622. oxidative
  56623. coupling
  56624. review
  56625. jerry
  56626. periodic
  56627. table
  56628. benzenoid
  56629. hydro
  56630. review
  56631. dickens
  56632. gilday
  56633. negri
  56634. widdowson
  56635. review
  56636. dickson
  56637. organometallic
  56638. chemistry
  56639. rhodium
  56640. review
  56641. kilian
  56642. carter
  56643. douglas
  56644. carbon
  56645. nuclear
  56646. review
  56647. dilling
  56648. polymerization
  56649. unsaturated
  56650. compounds
  56651. review
  56652. dimaio
  56653. anthony
  56654. joseph
  56655. rheingold
  56656. arnold
  56657. structural
  56658. review
  56659. dimroth
  56660. phosphorins
  56661. 198215
  56662. review
  56663. review
  56664. dittmer
  56665. donald
  56666. explorations
  56667. chalcogen
  56668. hetero
  56669. review
  56670. dixneuf
  56671. pierre
  56672. activation
  56673. alkynes
  56674. rutheni
  56675. review
  56676. dixneuf
  56677. pierre
  56678. activation
  56679. alkynes
  56680. rutheni
  56681. review
  56682. djerassi
  56683. sponge
  56684. phospholipids
  56685. review
  56686. doetz
  56687. heinz
  56688. carbene
  56689. complexes
  56690. stereoselecti
  56691. review
  56692. dolbier
  56693. koroniak
  56694. electrocyclic
  56695. review
  56696. dolbier
  56697. william
  56698. cycloadditions
  56699. fluoroallene
  56700. review
  56701. dolgoplosk
  56702. korshak
  56703. organometallic
  56704. catslysi
  56705. review
  56706. dolgoplosk
  56707. tinyakova
  56708. organometallic
  56709. catslys
  56710. review
  56711. dolphin
  56712. david
  56713. avramovic
  56714. poulson
  56715. rozanne
  56716. review
  56717. dombek
  56718. homogeneous
  56719. catalytic
  56720. hydrogenation
  56721. review
  56722. dombrovskii
  56723. halogen
  56724. derivatives
  56725. dioxan
  56726. review
  56727. dombrovskii
  56728. fonskii
  56729. mironov
  56730. synths
  56731. review
  56732. donaldson
  56733. william
  56734. palladium
  56735. mediated
  56736. methylenecyc
  56737. review
  56738. dondoni
  56739. alessandro
  56740. organometallic
  56741. reagents
  56742. review
  56743. dopke
  56744. eburnamine
  56745. vincamine
  56746. alkaloids
  56747. review
  56748. carbene
  56749. complexes
  56750. organic
  56751. synthesis
  56752. review
  56753. carbene
  56754. complexes
  56755. organic
  56756. synthesis
  56757. review
  56758. doubleday
  56759. charles
  56760. turro
  56761. nicholas
  56762. jinfeng
  56763. review
  56764. dougherty
  56765. dennis
  56766. control
  56767. organic
  56768. molecule
  56769. review
  56770. irngartinger
  56771. hermann
  56772. tricyclo
  56773. 2.1.0.025
  56774. review
  56775. drabowicz
  56776. mikolajczyk
  56777. synthesis
  56778. sulfoxides
  56779. review
  56780. drauz
  56781. kleemann
  56782. martens
  56783. induction
  56784. asymmetry
  56785. review
  56786. drewes
  56787. siegfried
  56788. gregory
  56789. synthetic
  56790. poten
  56791. review
  56792. properties
  56793. bonds
  56794. review
  56795. dubac
  56796. jacques
  56797. laporterie
  56798. andre
  56799. manuel
  56800. georges
  56801. group
  56802. review
  56803. dubois
  56804. rakowski
  56805. catalytic
  56806. applications
  56807. review
  56808. duerr
  56809. bouas
  56810. laurnnt
  56811. henri
  56812. photochromism
  56813. molec
  56814. review
  56815. duesler
  56816. structures
  56817. review
  56818. dugas
  56819. hermann
  56820. bioorganic
  56821. chemistry
  56822. chemical
  56823. appro
  56824. review
  56825. rudorf
  56826. carbon
  56827. disulphide
  56828. organi
  56829. review
  56830. peter
  56831. charles
  56832. novel
  56833. polysulfur
  56834. polyni
  56835. review
  56836. duran
  56837. singlet
  56838. oxygen
  56839. biological
  56840. processes
  56841. review
  56842. durkin
  56843. kathleen
  56844. sherrod
  56845. michael
  56846. liotta
  56847. dennis
  56848. review
  56849. perspectives
  56850. photochroism
  56851. novel
  56852. system
  56853. review
  56854. durst
  56855. techniques
  56856. carbanion
  56857. chemistry
  56858. comprehen
  56859. review
  56860. duthaler
  56861. rudolf
  56862. hafner
  56863. andreas
  56864. riediker
  56865. martin
  56866. review
  56867. breitmaier
  56868. synthesis
  56869. alkoxyacrolei
  56870. review
  56871. breuer
  56872. heterocycles
  56873. organic
  56874. review
  56875. matveeva
  56876. review
  56877. erdik
  56878. tetrahedron
  56879. tetrahedron
  56880. report
  56881. review
  56882. erdik
  56883. tetrahedron
  56884. activation
  56885. review
  56886. lukevits
  56887. segal
  56888. heterocycl
  56889. compds
  56890. review
  56891. negishi
  56892. controlled
  56893. carbom
  56894. review
  56895. denisov
  56896. khudyakov
  56897. review
  56898. eberhardt
  56899. manfred
  56900. homolytic
  56901. aromatic
  56902. hydroxylatio
  56903. review
  56904. eberson
  56905. electron
  56906. transfer
  56907. reactions
  56908. organic
  56909. review
  56910. ebetino
  56911. frank
  56912. degenhardt
  56913. charles
  56914. jamieson
  56915. laura
  56916. review
  56917. effenberger
  56918. franz
  56919. dialkylamino
  56920. benzenes
  56921. review
  56922. organic
  56923. chemistry
  56924. heath
  56925. lexingto
  56926. review
  56927. egorochkin
  56928. spectroscopy
  56929. organic
  56930. compound
  56931. review
  56932. einhorn
  56933. cathy
  56934. einhorn
  56935. jacques
  56936. luche
  56937. louis
  56938. review
  56939. eisch
  56940. sexsmith
  56941. stephen
  56942. intermediates
  56943. review
  56944. eisch
  56945. shafii
  56946. babak
  56947. boleslawski
  56948. marek
  56949. review
  56950. basil
  56951. sherif
  56952. caterpillar
  56953. gutman
  56954. trees
  56955. chemica
  56956. review
  56957. el'tsov
  56958. organic
  56959. photochromes
  56960. translated
  56961. review
  56962. elander
  56963. lactam
  56964. producing
  56965. microorganism
  56966. review
  56967. eliel
  56968. application
  56969. cram's
  56970. addition
  56971. review
  56972. eliel
  56973. prostereoisomerism
  56974. prochirality
  56975. review
  56976. whitton
  56977. sargent
  56978. recent
  56979. progress
  56980. review
  56981. ellis
  56982. highly
  56983. reduced
  56984. metal
  56985. carbonyl
  56986. anions
  56987. review
  56988. elnagdi
  56989. abdel
  56990. galil
  56991. elgemeie
  56992. review
  56993. elnagdi
  56994. elfahham
  56995. elgemeie
  56996. utility
  56997. review
  56998. elnagdi
  56999. elmoghayar
  57000. elgemeie
  57001. review
  57002. elnagdi
  57003. zayed
  57004. abdou
  57005. chemistry
  57006. heterocy
  57007. review
  57008. elnagdi
  57009. mohamed
  57010. hilmy
  57011. elmoghayer
  57012. mohamed
  57013. rifaat
  57014. review
  57015. elschenbroich
  57016. salzer
  57017. organometallics
  57018. concise
  57019. review
  57020. elsevier
  57021. muller
  57022. vrieze
  57023. selectiv
  57024. review
  57025. domsch
  57026. feger
  57027. frick
  57028. hergott
  57029. review
  57030. physicochemical
  57031. preconditions
  57032. linear
  57033. review
  57034. enders
  57035. alkylation
  57036. chiral
  57037. hydrazones
  57038. volume
  57039. review
  57040. engel
  57041. robert
  57042. phosphorus
  57043. addition
  57044. carbon
  57045. review
  57046. engelhardt
  57047. heinz
  57048. chromatographic
  57049. characterization
  57050. review
  57051. engels
  57052. uhlmann
  57053. synthesis
  57054. review
  57055. epsztein
  57056. formation
  57057. transformation
  57058. review
  57059. erastov
  57060. nikonov
  57061. tertiary
  57062. phosphines
  57063. review
  57064. erdik
  57065. copper
  57066. catalyzed
  57067. reactions
  57068. organolithi
  57069. review
  57070. erdik
  57071. ender
  57072. mehmet
  57073. electrophilic
  57074. amination
  57075. review
  57076. erickson
  57077. constituents
  57078. laurencia
  57079. marine
  57080. natur
  57081. review
  57082. erker
  57083. metallocene
  57084. carbene
  57085. complexes
  57086. related
  57087. review
  57088. erker
  57089. gerhard
  57090. aulbach
  57091. michael
  57092. miguel
  57093. pfaff
  57094. review
  57095. erker
  57096. gerhard
  57097. novel
  57098. structural
  57099. chemical
  57100. review
  57101. ershov
  57102. nikiforov
  57103. quinone
  57104. diazides
  57105. elsevier
  57106. review
  57107. ether
  57108. lipids
  57109. synthesis
  57110. application
  57111. tumor
  57112. review
  57113. etter
  57114. margaret
  57115. encoding
  57116. decoding
  57117. hydrogen
  57118. review
  57119. evans
  57120. nelson
  57121. taber
  57122. stereoselective
  57123. review
  57124. evans
  57125. stereoselective
  57126. alkylation
  57127. reactions
  57128. review
  57129. evans
  57130. studies
  57131. asymmetric
  57132. synthesis
  57133. devel
  57134. review
  57135. evans
  57136. taylor
  57137. inflammatory
  57138. tumour
  57139. promot
  57140. review
  57141. expanding
  57142. industrial
  57143. applications
  57144. palladium
  57145. review
  57146. mathey
  57147. angew
  57148. review
  57149. piozzi
  57150. rodriguez
  57151. savona
  57152. heterocycles
  57153. review
  57154. synth
  57155. optical
  57156. review
  57157. turecek
  57158. czech
  57159. commun
  57160. stereoch
  57161. review
  57162. fabian
  57163. zahradnik
  57164. search
  57165. highly
  57166. colored
  57167. review
  57168. fabre
  57169. devynck
  57170. tremillon
  57171. thermodynamic
  57172. behav
  57173. review
  57174. facelli
  57175. julio
  57176. grant
  57177. david
  57178. molecular
  57179. structure
  57180. review
  57181. heinz
  57182. chemistry
  57183. linear
  57184. oligopyrroles
  57185. review
  57186. farcasiu
  57187. protonation
  57188. simple
  57189. aromatics
  57190. super
  57191. review
  57192. farid
  57193. mattes
  57194. photochemical
  57195. electron
  57196. transfer
  57197. review
  57198. faulkner
  57199. glass
  57200. electrochemiiuminesc
  57201. chemica
  57202. review
  57203. fedorov
  57204. kravtsov
  57205. peregudov
  57206. metallotropi
  57207. review
  57208. fedorov
  57209. spectroscopy
  57210. review
  57211. fenselau
  57212. catherine
  57213. spectrometry
  57214. desorp
  57215. review
  57216. ferris
  57217. hagan
  57218. chemical
  57219. evolution
  57220. review
  57221. fetizon
  57222. marcel
  57223. goulaouic
  57224. pierre
  57225. hanna
  57226. issam
  57227. review
  57228. fetzer
  57229. synthesis
  57230. large
  57231. condensed
  57232. polycycl
  57233. review
  57234. synth
  57235. optical
  57236. review
  57237. feuer
  57238. henry
  57239. nielsen
  57240. arnold
  57241. nitro
  57242. compounds
  57243. review
  57244. fleming
  57245. dunogues
  57246. jacques
  57247. smithers
  57248. roger
  57249. review
  57250. fraser
  57251. effect
  57252. enolate
  57253. review
  57254. fuerstner
  57255. alois
  57256. recent
  57257. advancements
  57258. reformat@
  57259. review
  57260. shvekhgeimer
  57261. zvolinskii
  57262. kobrakov
  57263. review
  57264. kabalka
  57265. organomet
  57266. boron
  57267. boran@
  57268. review
  57269. lattes
  57270. perie
  57271. amination
  57272. alkenes
  57273. review
  57274. giese
  57275. isoselective
  57276. relationship
  57277. 198417
  57278. review
  57279. glass
  57280. richard
  57281. conformational
  57282. analysis
  57283. mediu@
  57284. review
  57285. goldschmidt
  57286. crammer
  57287. vinylcyclopropane
  57288. rearrange
  57289. review
  57290. granik
  57291. influence
  57292. properties
  57293. review
  57294. grimes
  57295. russell
  57296. small
  57297. carboranes
  57298. building
  57299. block@
  57300. review
  57301. gupta
  57302. physical
  57303. methods
  57304. heterocyclic
  57305. chemi@
  57306. review
  57307. feuer
  57308. henry
  57309. nielsen
  57310. arnold
  57311. nitro
  57312. compounds
  57313. review
  57314. fiandanese
  57315. sequential
  57316. cross
  57317. coupling
  57318. reactions
  57319. review
  57320. scriven
  57321. cyanation
  57322. pyridine
  57323. review
  57324. filippova
  57325. blyumberg
  57326. mechanism
  57327. epoxid
  57328. review
  57329. filler
  57330. nonbonded
  57331. interactions
  57332. between
  57333. arenes
  57334. review
  57335. fillol
  57336. miranda
  57337. miguel
  57338. morera
  57339. isabel
  57340. sheikh
  57341. review
  57342. finet
  57343. piere
  57344. arylation
  57345. reactions
  57346. organobis
  57347. review
  57348. fischer
  57349. hofmann
  57350. kreissl
  57351. schrock
  57352. schuber
  57353. review
  57354. fischer
  57355. hofmann
  57356. kreissl
  57357. schrock
  57358. schuher
  57359. review
  57360. fischer
  57361. kreissl
  57362. spectroscopic
  57363. properties
  57364. review
  57365. fischer
  57366. mechanistic
  57367. aspects
  57368. carbene
  57369. complexes
  57370. review
  57371. fischer
  57372. synthesis
  57373. carbene
  57374. complexes
  57375. transi
  57376. review
  57377. fisher
  57378. lawrence
  57379. muchowski
  57380. joseph
  57381. synthesis
  57382. review
  57383. fleet
  57384. george
  57385. homochiral
  57386. compounds
  57387. sugars
  57388. review
  57389. fleming
  57390. silicon
  57391. mediated
  57392. stereochemically
  57393. control
  57394. review
  57395. fleming
  57396. dunogues
  57397. jacques
  57398. smithers
  57399. roger
  57400. review
  57401. flitsch
  57402. wilhelm
  57403. hydrogenated
  57404. porphyrin
  57405. derivatives
  57406. review
  57407. flitsch
  57408. wilhelm
  57409. chemistry
  57410. azaazulenes
  57411. review
  57412. floss
  57413. beale
  57414. biosynthetic
  57415. studies
  57416. antibio
  57417. review
  57418. floss
  57419. stereochemistry
  57420. biological
  57421. review
  57422. fokin
  57423. allakhverdiev
  57424. kolomiets
  57425. advan
  57426. review
  57427. fokin
  57428. kolomiets
  57429. vasil'ev
  57430. fluorine
  57431. conta
  57432. review
  57433. fokin
  57434. sudnev
  57435. kuznetsova
  57436. krotovich
  57437. review
  57438. formosinho
  57439. sabastiao
  57440. arnaut
  57441. unified
  57442. review
  57443. forsyth
  57444. isotope
  57445. effects
  57446. shifts
  57447. review
  57448. membered
  57449. cyclic
  57450. nitrones
  57451. synthesis
  57452. reactiv
  57453. review
  57454. organic
  57455. heterogeneous
  57456. photocatalysis
  57457. chemic
  57458. review
  57459. franck
  57460. mycotoxins
  57461. fungi
  57462. structures
  57463. review
  57464. franck
  57465. topical
  57466. problems
  57467. biosynthesis
  57468. review
  57469. fraser
  57470. nuclear
  57471. magnetic
  57472. resonance
  57473. analysis
  57474. review
  57475. fraser
  57476. effect
  57477. enolate
  57478. review
  57479. fraser
  57480. mootoo
  57481. randy
  57482. konradsson
  57483. peter
  57484. review
  57485. frauenrath
  57486. herbert
  57487. vinyl
  57488. acetals
  57489. related
  57490. compou
  57491. review
  57492. freedman
  57493. preparation
  57494. reactions
  57495. review
  57496. freeman
  57497. fillmore
  57498. darrick
  57499. rodriguez
  57500. review
  57501. freeman
  57502. fillmore
  57503. chemistry
  57504. dithiins
  57505. review
  57506. freeman
  57507. isoxazolines
  57508. dihydroisoxazoles
  57509. review
  57510. freeman
  57511. jermiah
  57512. organic
  57513. syntheses
  57514. collective
  57515. review
  57516. fresenius
  57517. phillip
  57518. organic
  57519. chemical
  57520. nomenclature
  57521. review
  57522. stereochemistry
  57523. enzymatic
  57524. reactions
  57525. review
  57526. friedrichsen
  57527. kappe
  57528. bottcher
  57529. membered
  57530. review
  57531. fringuelli
  57532. francesco
  57533. taticchi
  57534. dienes
  57535. review
  57536. fringuelli
  57537. franceso
  57538. taticchi
  57539. wenkert
  57540. ernest
  57541. review
  57542. albert
  57543. synthetic
  57544. organic
  57545. electrochemistry
  57546. review
  57547. fryzuk
  57548. michael
  57549. functionalization
  57550. alkynes
  57551. enyne
  57552. review
  57553. fuerstner
  57554. alois
  57555. recent
  57556. advancements
  57557. reformat
  57558. review
  57559. fuhrhop
  57560. penzlin
  57561. organic
  57562. synthesis
  57563. verlag
  57564. chemie
  57565. review
  57566. lythraceous
  57567. alkaloids
  57568. alkaloids
  57569. chemistr
  57570. review
  57571. fujii
  57572. ipecac
  57573. alkaloids
  57574. carboline
  57575. review
  57576. fujita
  57577. eiichi
  57578. nagao
  57579. yoshimitsu
  57580. chiral
  57581. induction
  57582. review
  57583. fujita
  57584. substituent
  57585. effects
  57586. partition
  57587. coeff
  57588. review
  57589. fujiwara
  57590. iintoku
  57591. tetsuro
  57592. takaki
  57593. review
  57594. fukui
  57595. frontier
  57596. orbitals
  57597. chemical
  57598. review
  57599. fukuto
  57600. jensen
  57601. mechanisms
  57602. reactions
  57603. review
  57604. funayama
  57605. cordell
  57606. polymerization
  57607. and/or
  57608. rearra
  57609. review
  57610. furin
  57611. bardin
  57612. higher
  57613. fluorides
  57614. group
  57615. review
  57616. furin
  57617. electrophilic
  57618. fluorination
  57619. agents
  57620. review
  57621. furmanova
  57622. crystal
  57623. structures
  57624. potentially
  57625. review
  57626. electrophilic
  57627. review
  57628. formylating
  57629. review
  57630. shvekhgeimer
  57631. zvolinskii
  57632. kobrakov
  57633. review
  57634. marquardt
  57635. synthesis
  57636. review
  57637. posner
  57638. asymmetric
  57639. synth
  57640. review
  57641. sugden
  57642. waghela
  57643. synthesis
  57644. review
  57645. heinisch
  57646. heterocycles
  57647. advances
  57648. review
  57649. kresze
  57650. ascherl
  57651. braun
  57652. felber
  57653. review
  57654. larson
  57655. organomet
  57656. organosili
  57657. review
  57658. l'abbe
  57659. synthesis
  57660. membered
  57661. heterocycl
  57662. review
  57663. transition
  57664. metal
  57665. review
  57666. mohiuddin
  57667. reddy
  57668. ahmed
  57669. ratnam
  57670. hetero
  57671. review
  57672. freedman
  57673. organomet
  57674. review
  57675. ellis
  57676. romney
  57677. alexander
  57678. review
  57679. tetrahedron
  57680. carbon
  57681. review
  57682. tetrahedron
  57683. carbon
  57684. review
  57685. newkome
  57686. baker
  57687. proced
  57688. review
  57689. kabalka
  57690. organomet
  57691. boron
  57692. boran
  57693. review
  57694. kabalka
  57695. organomet
  57696. boron
  57697. review
  57698. gajewski
  57699. joseph
  57700. gilbert
  57701. kevin
  57702. mckelvey
  57703. review
  57704. franc
  57705. maria
  57706. pierre
  57707. charles
  57708. correlation
  57709. review
  57710. gallo
  57711. makosza
  57712. hassanaly
  57713. applicati
  57714. review
  57715. gallo
  57716. treatment
  57717. steric
  57718. effects
  57719. 198314115
  57720. review
  57721. gallo
  57722. roger
  57723. roussel
  57724. christian
  57725. quantita
  57726. review
  57727. gamayurova
  57728. basicity
  57729. nucleophilicity
  57730. review
  57731. ganem
  57732. chemistry
  57733. naturally
  57734. occurring
  57735. polyam
  57736. review
  57737. gante
  57738. azapeptides
  57739. synthesis
  57740. review
  57741. garegg
  57742. artificial
  57743. antigens
  57744. prospects
  57745. medicine
  57746. review
  57747. garin
  57748. francois
  57749. maire
  57750. gilbert
  57751. possible
  57752. surface
  57753. inter
  57754. review
  57755. garratt
  57756. peter
  57757. payne
  57758. david
  57759. tsotinis
  57760. andrew
  57761. battere
  57762. review
  57763. garrou
  57764. redistribution
  57765. reactiors
  57766. transition
  57767. review
  57768. garst
  57769. grignard
  57770. reagent
  57771. formation
  57772. freely
  57773. review
  57774. lattes
  57775. perie
  57776. amination
  57777. alkenes
  57778. review
  57779. gassman
  57780. tidwell
  57781. electron
  57782. deficient
  57783. carbocat
  57784. review
  57785. gault
  57786. mechanisms
  57787. skeletal
  57788. isomerization
  57789. review
  57790. gavezzotti
  57791. simonetta
  57792. crystal
  57793. chemistry
  57794. organ
  57795. review
  57796. gawronski
  57797. circular
  57798. dichroism
  57799. stereochemistr
  57800. review
  57801. gazizov
  57802. khairullin
  57803. moskva
  57804. reactions
  57805. review
  57806. gel'mbol'dt
  57807. ennan
  57808. pentacoordinate
  57809. fluorosil
  57810. review
  57811. geoffroy
  57812. gregory
  57813. bassner
  57814. sherri
  57815. interaction
  57816. review
  57817. geoffroy
  57818. gregory
  57819. sheridan
  57820. bassner
  57821. sherri
  57822. review
  57823. gerson
  57824. radical
  57825. phanes
  57826. studied
  57827. review
  57828. gerzon
  57829. svoboda
  57830. acridone
  57831. alkaloids
  57832. experimenta
  57833. review
  57834. getchell
  57835. getchell
  57836. physiology
  57837. vertebrate
  57838. review
  57839. gielen
  57840. chirality
  57841. static
  57842. dynamic
  57843. stereochemist
  57844. review
  57845. gielen
  57846. marcel
  57847. topics
  57848. physical
  57849. organometallic
  57850. review
  57851. giese
  57852. isoselective
  57853. relationship
  57854. 198417
  57855. review
  57856. giese
  57857. isoselective
  57858. relationship
  57859. 198417
  57860. review
  57861. giese
  57862. bernd
  57863. stereoselective
  57864. syntheses
  57865. carbohyd
  57866. review
  57867. giese
  57868. bernd
  57869. stereoselectivity
  57870. intermolecular
  57871. review
  57872. synthesis
  57873. glycolipids
  57874. 1990154
  57875. review
  57876. giguere
  57877. raymond
  57878. nonconventional
  57879. reaction
  57880. conditio
  57881. review
  57882. gilchrist
  57883. heterocyclic
  57884. chemistry
  57885. wiley
  57886. newyork
  57887. review
  57888. gilchrist
  57889. nitroso
  57890. alkenes
  57891. nitroso
  57892. alkynes
  57893. review
  57894. gilday
  57895. paquette
  57896. carbon
  57897. carbon
  57898. review
  57899. developments
  57900. chemiluminescence
  57901. review
  57902. gilyarov
  57903. phosphorus
  57904. azides
  57905. review
  57906. ginsburg
  57907. secondary
  57908. orbital
  57909. interactio
  57910. review
  57911. giordano
  57912. castaldi
  57913. uggeri
  57914. synthesis
  57915. review
  57916. gladysz
  57917. synthetic
  57918. chemistry
  57919. transition
  57920. review
  57921. gladysz
  57922. transition
  57923. metal
  57924. formyl
  57925. complexes
  57926. review
  57927. glass
  57928. richard
  57929. andruski
  57930. stephen
  57931. broeker
  57932. jeffrey
  57933. review
  57934. glass
  57935. richard
  57936. conformational
  57937. analysis
  57938. mediu
  57939. review
  57940. glebov
  57941. kliger
  57942. syntheses
  57943. organic
  57944. compound
  57945. review
  57946. gleiter
  57947. paquette
  57948. interaction
  57949. control
  57950. review
  57951. gleiter
  57952. schaefer
  57953. wolfgang
  57954. interactions
  57955. between
  57956. review
  57957. glese
  57958. formation
  57959. bonds
  57960. addition
  57961. review
  57962. godleski
  57963. schleyer
  57964. osawa
  57965. wipke
  57966. review
  57967. godovikova
  57968. rakitin
  57969. khmel'nitskii
  57970. diazot
  57971. review
  57972. gokel
  57973. dishong
  57974. schultz
  57975. gatto
  57976. synthes
  57977. review
  57978. gokel
  57979. korzeniowski
  57980. macrocyclic
  57981. polyether
  57982. review
  57983. gokel
  57984. george
  57985. arnold
  57986. delgado
  57987. echeverria
  57988. review
  57989. gol'dberg
  57990. sturkovich
  57991. lukevics
  57992. heterocyclic
  57993. review
  57994. goldberg
  57995. significance
  57996. molecular
  57997. shape
  57998. review
  57999. golding
  58000. bernard
  58001. synthesis
  58002. reactions
  58003. chiral
  58004. review
  58005. golding
  58006. bernard
  58007. mystery
  58008. chemis
  58009. review
  58010. goldschmidt
  58011. crammer
  58012. vinylcyclopropane
  58013. rearrange
  58014. review
  58015. goldschmidt
  58016. crammer
  58017. vinylcyclopropane
  58018. rearrange
  58019. review
  58020. gololobov
  58021. gusar
  58022. tarasevich
  58023. three
  58024. membe
  58025. review
  58026. gonzalez
  58027. antonio
  58028. galindo
  58029. mansilla
  58030. biomimetic
  58031. review
  58032. gordon
  58033. sykes
  58034. cephamycin
  58035. antibiotics
  58036. chemist
  58037. review
  58038. gordon
  58039. isabel
  58040. maskill
  58041. ruasse
  58042. marie
  58043. francoise
  58044. review
  58045. gordon
  58046. isobel
  58047. maskill
  58048. ruasse
  58049. marie
  58050. francoise
  58051. review
  58052. gorelik
  58053. current
  58054. state
  58055. problem
  58056. aromati
  58057. review
  58058. gorenstein
  58059. biological
  58060. aspects
  58061. phosphorus
  58062. review
  58063. toshio
  58064. kondo
  58065. tadao
  58066. structure
  58067. molecular
  58068. review
  58069. gould
  58070. turro
  58071. zimmi
  58072. magnetic
  58073. field
  58074. review
  58075. govundachari
  58076. chinnasamy
  58077. rajeswari
  58078. chandrase
  58079. review
  58080. gragerov
  58081. skrunts
  58082. geller
  58083. kinetics
  58084. review
  58085. grandbois
  58086. howard
  58087. morrison
  58088. reductions
  58089. review
  58090. granik
  58091. advances
  58092. chemistry
  58093. enamines
  58094. review
  58095. granik
  58096. advances
  58097. chemistry
  58098. amidines
  58099. review
  58100. granik
  58101. influence
  58102. properties
  58103. review
  58104. grant
  58105. david
  58106. higuchi
  58107. takeru
  58108. solubility
  58109. behavior
  58110. review
  58111. grasselli
  58112. burrington
  58113. selective
  58114. oxidation
  58115. review
  58116. computer
  58117. assisted
  58118. analysis
  58119. carbon
  58120. review
  58121. grebenik
  58122. peter
  58123. grinter
  58124. roger
  58125. perutz
  58126. robin
  58127. metallo
  58128. review
  58129. acyclic
  58130. butadiene
  58131. tricarbonyl
  58132. complexes
  58133. review
  58134. green
  58135. lambeth
  58136. leukotrienes
  58137. review
  58138. greenhill
  58139. quinolines
  58140. jones
  58141. gurnos
  58142. review
  58143. greenwood
  58144. norman
  58145. kennedy
  58146. thought
  58147. review
  58148. gribble
  58149. gordon
  58150. synthesis
  58151. antitumor
  58152. activity
  58153. review
  58154. gribble
  58155. gordon
  58156. synthetic
  58157. approaches
  58158. ellipt
  58159. review
  58160. grierson
  58161. david
  58162. polonovski
  58163. reaction
  58164. review
  58165. griffin
  58166. marchand
  58167. synthesis
  58168. chemis
  58169. review
  58170. griffith
  58171. william
  58172. stephen
  58173. tetra
  58174. npropyl
  58175. review
  58176. griller
  58177. david
  58178. wayner
  58179. danial
  58180. radical
  58181. thermochemi
  58182. review
  58183. grimes
  58184. russell
  58185. small
  58186. carboranes
  58187. building
  58188. block
  58189. review
  58190. grimmett
  58191. keene
  58192. reactions
  58193. annular
  58194. nitro
  58195. review
  58196. grinberg
  58197. modern
  58198. layer
  58199. chromatography
  58200. review
  58201. inductivity
  58202. bridging
  58203. carbocations
  58204. review
  58205. norbornyl
  58206. cation
  58207. prototype
  58208. review
  58209. gruenanger
  58210. paolo
  58211. finzi
  58212. paola
  58213. isoxazoles
  58214. review
  58215. grundon
  58216. quinoline
  58217. alkaloids
  58218. related
  58219. anthrani
  58220. review
  58221. grunwald
  58222. ernest
  58223. reaction
  58224. coordinates
  58225. structure
  58226. review
  58227. grunwald
  58228. ernest
  58229. thermodynamics
  58230. molecular
  58231. species
  58232. review
  58233. gryaznov
  58234. gul'yanova
  58235. serov
  58236. review
  58237. guette
  58238. creene
  58239. bulliot
  58240. henri
  58241. desmurs
  58242. review
  58243. guggisberg
  58244. hesse
  58245. putrescine
  58246. spermidine
  58247. spermine
  58248. review
  58249. guindon
  58250. anderson
  58251. yoakim
  58252. christiane
  58253. review
  58254. hyushin
  58255. golod
  58256. gidaspov
  58257. nitroni
  58258. review
  58259. gupta
  58260. bioactive
  58261. molecules
  58262. phenothiazin
  58263. review
  58264. gupta
  58265. physical
  58266. methods
  58267. heterocyclic
  58268. chemi
  58269. review
  58270. gupta
  58271. singh
  58272. bindal
  58273. studies
  58274. halluc
  58275. review
  58276. gurjar
  58277. mukund
  58278. synthesis
  58279. enantiomerically
  58280. review
  58281. gusarova
  58282. voronkov
  58283. trofimov
  58284. divinyl
  58285. review
  58286. devens
  58287. moore
  58288. thomas
  58289. mimicking
  58290. photosynthetic
  58291. review
  58292. guthrie
  58293. thermodynamics
  58294. metastable
  58295. intermedia
  58296. review
  58297. guthrie
  58298. robert
  58299. jencks
  58300. wiliam
  58301. iupac
  58302. recommendati
  58303. review
  58304. gutman
  58305. david
  58306. controversial
  58307. formation
  58308. review
  58309. gutman
  58310. cyvin
  58311. introduction
  58312. theory
  58313. review
  58314. gutsche
  58315. calixarenes
  58316. 198316161
  58317. review
  58318. accounts
  58319. review
  58320. gutsche
  58321. calixarenes
  58322. royal
  58323. society
  58324. chemistry
  58325. review
  58326. gutsche
  58327. iqbal
  58328. conformati
  58329. review
  58330. gutsche
  58331. calixarenes
  58332. topics
  58333. review
  58334. gutsche
  58335. david
  58336. rogers
  58337. janet
  58338. stewart
  58339. donald
  58340. review
  58341. guziec
  58342. frank
  58343. sanfilippo
  58344. james
  58345. synthetical
  58346. review
  58347. kagan
  58348. tetrahedron
  58349. review
  58350. dammel
  58351. angew
  58352. review
  58353. brunner
  58354. leyerer
  58355. review
  58356. brown
  58357. prasad
  58358. heterocycles
  58359. review
  58360. colquhoun
  58361. london
  58362. homogeneous
  58363. review
  58364. simonyi
  58365. alderweireldt
  58366. review
  58367. organic
  58368. radical
  58369. review
  58370. zimmerman
  58371. kinetic
  58372. review
  58373. wasserman
  58374. aldrichimica
  58375. review
  58376. hartmann
  58377. klemm
  58378. biologicall
  58379. review
  58380. hashimoto
  58381. kawaguchi
  58382. synth
  58383. review
  58384. heimgartner
  58385. application
  58386. review
  58387. kagan
  58388. chemistry
  58389. review
  58390. kosugi
  58391. synth
  58392. asymmetri
  58393. review
  58394. angew
  58395. synthesis
  58396. review
  58397. kagan
  58398. tetrahedron
  58399. review
  58400. heterocycles
  58401. review
  58402. hamilton
  58403. andrew
  58404. hydrogen
  58405. binding
  58406. biological
  58407. review
  58408. harrington
  58409. peter
  58410. transition
  58411. metals
  58412. total
  58413. synth@
  58414. review
  58415. wenchen
  58416. wenjie
  58417. valley
  58418. method
  58419. review
  58420. hendrickson
  58421. james
  58422. organic
  58423. synthesis
  58424. review
  58425. hiemstra
  58426. speckamp
  58427. acyliminium
  58428. inter
  58429. review
  58430. hoffmann
  58431. cycloaddition
  58432. allyl
  58433. cations
  58434. review
  58435. multibridged
  58436. cyclophanes
  58437. cyclophanes
  58438. review
  58439. housecroft
  58440. fehlner
  58441. metalloboranes
  58442. their
  58443. review
  58444. huisgen
  58445. kinetics
  58446. reaction
  58447. mechanisms
  58448. selec@
  58449. review
  58450. imamoto
  58451. tsuneo
  58452. synthetic
  58453. methods
  58454. lanthanid@
  58455. review
  58456. masayoshi
  58457. recent
  58458. progress
  58459. synthesis
  58460. review
  58461. fluorine
  58462. synposium
  58463. proceedings
  58464. review
  58465. kagan
  58466. tetrahedron
  58467. review
  58468. mague
  58469. organomet
  58470. cobalt
  58471. rhodi@
  58472. review
  58473. kuczkowski
  58474. formation
  58475. structures
  58476. ozonides@
  58477. review
  58478. matteson
  58479. donald
  58480. alpha
  58481. boronic
  58482. esters
  58483. interme@
  58484. review
  58485. malhotra
  58486. narang
  58487. nitration
  58488. methods
  58489. review
  58490. regitz
  58491. manfred
  58492. phosphaalkynes
  58493. building
  58494. blocks
  58495. review
  58496. shockman
  58497. daneo
  58498. moore
  58499. mcdowell
  58500. review
  58501. tramontini
  58502. maurilio
  58503. angiolini
  58504. luigi
  58505. further
  58506. advance@
  58507. review
  58508. yashin
  58509. chromatographic
  58510. retention
  58511. parameters
  58512. survey
  58513. radical
  58514. mediated
  58515. cyclization
  58516. acetals
  58517. acetylacetonate@
  58518. aciral@
  58519. activation
  58520. alkynes
  58521. ruthenium
  58522. complexes@
  58523. acyl@
  58524. advances
  58525. amination
  58526. nitrogen
  58527. heterocycles@
  58528. aldol
  58529. condensations
  58530. procedures
  58531. available
  58532. card@
  58533. alkaloids
  58534. nitrones@
  58535. application
  58536. anhydrous
  58537. hydrogen
  58538. fluoride
  58539. structura@
  58540. review
  58541. heterocycles
  58542. review
  58543. suzuki
  58544. synth
  58545. organic
  58546. review
  58547. takahata
  58548. yamazaki
  58549. synth
  58550. review
  58551. takaku
  58552. synth
  58553. recent
  58554. review
  58555. viola
  58556. reagents
  58557. thiolation
  58558. review
  58559. haaland
  58560. covalent
  58561. versus
  58562. dative
  58563. bonds
  58564. review
  58565. hafez
  58566. elmoghayer
  58567. agamey
  58568. review
  58569. hafner
  58570. klaus
  58571. novel
  58572. pentafulvenes
  58573. versatile
  58574. building
  58575. review
  58576. haines
  58577. methods
  58578. oxidation
  58579. organic
  58580. review
  58581. haldna
  58582. estimation
  58583. basicity
  58584. constants
  58585. review
  58586. forming
  58587. initiation
  58588. spontaneous
  58589. review
  58590. shekell
  58591. bredt
  58592. bridgehead
  58593. review
  58594. halpern
  58595. formation
  58596. carbon
  58597. hydrogen
  58598. bonds
  58599. review
  58600. halton
  58601. brian
  58602. alkylidenecyclopropa
  58603. strained
  58604. review
  58605. halton
  58606. brian
  58607. developments
  58608. cycloproparene
  58609. chemist
  58610. review
  58611. hamilton
  58612. andrew
  58613. hydrogen
  58614. binding
  58615. biological
  58616. review
  58617. hammerich
  58618. parker
  58619. kinetics
  58620. mechanism
  58621. review
  58622. hanaoka
  58623. transformation
  58624. reactions
  58625. protoberberin
  58626. review
  58627. hanessian
  58628. design
  58629. implementation
  58630. tactical
  58631. review
  58632. hanessian
  58633. synthetic
  58634. design
  58635. chiral
  58636. templates
  58637. review
  58638. hanessian
  58639. stephen
  58640. franco
  58641. jonathan
  58642. larouche
  58643. benoit
  58644. review
  58645. hansch
  58646. corwin
  58647. survey
  58648. hammett
  58649. review
  58650. happel
  58651. sellers
  58652. analysis
  58653. possible
  58654. mecha
  58655. review
  58656. harada
  58657. yoshiya
  58658. penning
  58659. ionization
  58660. electron
  58661. spectros
  58662. review
  58663. harborne
  58664. flavonoids
  58665. advances
  58666. research
  58667. review
  58668. harding
  58669. stephen
  58670. macrostructure
  58671. mucus
  58672. glyco
  58673. review
  58674. hardy
  58675. chemistry
  58676. pyrazolopyridines
  58677. review
  58678. hargittai
  58679. istvan
  58680. hargittai
  58681. magdolna
  58682. stereochemi
  58683. review
  58684. hargittai
  58685. istvan
  58686. variations
  58687. molecular
  58688. geometry
  58689. review
  58690. harre
  58691. raddatz
  58692. walenta
  58693. winterfeldt
  58694. review
  58695. harrington
  58696. peter
  58697. transition
  58698. metals
  58699. total
  58700. synth
  58701. review
  58702. david
  58703. ester
  58704. enolate
  58705. imine
  58706. review
  58707. hartley
  58708. patai
  58709. nature
  58710. cleavage
  58711. review
  58712. hartley
  58713. frank
  58714. chemistry
  58715. metal
  58716. carbo
  58717. review
  58718. hartwig
  58719. modern
  58720. methods
  58721. radical
  58722. deoxygenat
  58723. review
  58724. koskimies
  58725. compilation
  58726. references
  58727. review
  58728. hashimoto
  58729. shudo
  58730. okamoto
  58731. mutagenic
  58732. chemistry
  58733. review
  58734. hashimoto
  58735. yohei
  58736. kawanishi
  58737. kazuko
  58738. ichimnru
  58739. momoyo
  58740. review
  58741. haslam
  58742. metabolism
  58743. gallic
  58744. hexahydr
  58745. review
  58746. hassenruck
  58747. karin
  58748. martin
  58749. dieter
  58750. walsh
  58751. robin
  58752. review
  58753. tsujiaki
  58754. solution
  58755. prohlem
  58756. review
  58757. haubenstock
  58758. asymmetric
  58759. reductions
  58760. chiral
  58761. review
  58762. haufe
  58763. gunter
  58764. gerhard
  58765. chemistry
  58766. alicyclic
  58767. review
  58768. hayashi
  58769. kumada
  58770. asymmetric
  58771. synthesis
  58772. catalyzed
  58773. review
  58774. hayatsu
  58775. scott
  58776. winans
  58777. oxidation
  58778. review
  58779. wenchen
  58780. wenjie
  58781. valley
  58782. method
  58783. review
  58784. hearn
  58785. recent
  58786. progress
  58787. synthesis
  58788. review
  58789. heathcock
  58790. stereoselective
  58791. aldol
  58792. condensation
  58793. review
  58794. heathcock
  58795. aldol
  58796. addition
  58797. reaction
  58798. volume
  58799. review
  58800. heathcock
  58801. clayton
  58802. piettre
  58803. seige
  58804. mechani
  58805. review
  58806. heathcock
  58807. clayton
  58808. understanding
  58809. controlling
  58810. review
  58811. palladium
  58812. catalyzed
  58813. vinylation
  58814. organic
  58815. review
  58816. heelis
  58817. photophysical
  58818. photochemical
  58819. review
  58820. hegedus
  58821. formation
  58822. carbon
  58823. carbon
  58824. bonds
  58825. review
  58826. hegedus
  58827. palladium
  58828. assisted
  58829. reactions
  58830. review
  58831. hegedus
  58832. louis
  58833. chromium
  58834. carbene
  58835. complexes
  58836. review
  58837. heicklen
  58838. julian
  58839. decomposition
  58840. alkyl
  58841. nitrites
  58842. review
  58843. heilbronner
  58844. electronic
  58845. structure
  58846. review
  58847. heine
  58848. diaziridines
  58849. diazirines
  58850. diaziridinones
  58851. review
  58852. helquist
  58853. development
  58854. carbene
  58855. complexes
  58856. review
  58857. hendrickson
  58858. james
  58859. organic
  58860. synthesis
  58861. review
  58862. hermecz
  58863. meszaros
  58864. chemistry
  58865. pyrido
  58866. pyrim
  58867. review
  58868. herout
  58869. sesquiterpene
  58870. alcohols
  58871. fragrance
  58872. chemistry
  58873. review
  58874. herrmann
  58875. organometallic
  58876. aspects
  58877. fischer
  58878. review
  58879. herrmann
  58880. methylene
  58881. bridge
  58882. 20160
  58883. advanc
  58884. review
  58885. hewitt
  58886. christopher
  58887. silvester
  58888. michael
  58889. fluoroarom
  58890. review
  58891. hewitt
  58892. david
  58893. chemistry
  58894. azaphosphorins
  58895. review
  58896. hewlins
  58897. oliveira
  58898. campos
  58899. shannon
  58900. review
  58901. hibbert
  58902. frank
  58903. emsley
  58904. hydrogen
  58905. bonding
  58906. review
  58907. hiberty
  58908. philippe
  58909. charles
  58910. distortive
  58911. tendencies
  58912. review
  58913. hickmott
  58914. enamines
  58915. recent
  58916. advances
  58917. synthetic
  58918. review
  58919. hickmott
  58920. recent
  58921. advances
  58922. chemistry
  58923. review
  58924. hicks
  58925. kevin
  58926. performance
  58927. liquid
  58928. chromatograph
  58929. review
  58930. hideg
  58931. kalman
  58932. novel
  58933. potentially
  58934. useful
  58935. label
  58936. review
  58937. hiemstra
  58938. speckamp
  58939. acyliminium
  58940. inter
  58941. review
  58942. hiemstra
  58943. speckamp
  58944. acyliminium
  58945. inter
  58946. review
  58947. highsmith
  58948. thomas
  58949. meyers
  58950. albert
  58951. asymmetric
  58952. review
  58953. hilgenfeld
  58954. saenger
  58955. structural
  58956. chemistry
  58957. review
  58958. craig
  58959. activation
  58960. functionalization
  58961. review
  58962. chirality
  58963. transfer
  58964. sigmatropic
  58965. rearran
  58966. review
  58967. ribosomal
  58968. protein
  58969. synthesis
  58970. structure
  58971. review
  58972. nakagawa
  58973. chemistry
  58974. reactions
  58975. cyclic
  58976. review
  58977. hinton
  58978. briggs
  58979. thallium
  58980. spectro
  58981. review
  58982. hirama
  58983. masahiro
  58984. asymmetric
  58985. induction
  58986. review
  58987. hiraoka
  58988. crown
  58989. compounds
  58990. kodansha
  58991. tokyo
  58992. review
  58993. hirschmann
  58994. hanson
  58995. factoring
  58996. chirality
  58997. review
  58998. contrapolarization
  58999. concept
  59000. organic
  59001. review
  59002. through
  59003. modulation
  59004. reaction
  59005. centers
  59006. review
  59007. carbocycle
  59008. construction
  59009. terpene
  59010. synth
  59011. review
  59012. hoffman
  59013. robert
  59014. bartsch
  59015. richard
  59016. review
  59017. hoffmann
  59018. cycloaddition
  59019. allyl
  59020. cations
  59021. review
  59022. hoffmann
  59023. building
  59024. bridges
  59025. between
  59026. inorganic
  59027. review
  59028. hoffmann
  59029. diastereogenic
  59030. addition
  59031. crotylmetal
  59032. review
  59033. hoffmann
  59034. reinhard
  59035. chiral
  59036. allylboronates
  59037. reagent
  59038. review
  59039. hoffmann
  59040. reinhard
  59041. allylic
  59042. strain
  59043. controll
  59044. review
  59045. hoffmann
  59046. roald
  59047. laszlo
  59048. pierre
  59049. representation
  59050. review
  59051. hofmann
  59052. electronic
  59053. structures
  59054. transition
  59055. metal
  59056. review
  59057. holden
  59058. total
  59059. synthesis
  59060. penicillins
  59061. cephalosp
  59062. review
  59063. holder
  59064. chemistry
  59065. hexenuloses
  59066. review
  59067. holland
  59068. biotransformations
  59069. ketosteroids
  59070. review
  59071. holland
  59072. methyl
  59073. group
  59074. removal
  59075. steroid
  59076. biosynt
  59077. review
  59078. holland
  59079. mechanism
  59080. microbial
  59081. hydroxyl
  59082. review
  59083. hollingsworth
  59084. mcbride
  59085. michael
  59086. photochemica
  59087. review
  59088. holmes
  59089. robert
  59090. organotin
  59091. cluster
  59092. chemistry
  59093. review
  59094. holmes
  59095. robert
  59096. stereochemistry
  59097. nucleophilic
  59098. review
  59099. multibridged
  59100. cyclophanes
  59101. cyclophanes
  59102. review
  59103. hoppe
  59104. dieter
  59105. kraerner
  59106. thoms
  59107. schwark
  59108. robert
  59109. review
  59110. horner
  59111. leopold
  59112. retrospective
  59113. logic
  59114. review
  59115. hornfeldt
  59116. selenophenes
  59117. 30127
  59118. advances
  59119. review
  59120. horton
  59121. derek
  59122. hawkins
  59123. mcgarvey
  59124. glenn
  59125. review
  59126. horwitz
  59127. shriver
  59128. bonded
  59129. metal
  59130. carbon
  59131. review
  59132. hoshino
  59133. umezawa
  59134. tetraacetate
  59135. oxidation
  59136. review
  59137. hosmane
  59138. narayan
  59139. maguire
  59140. syntheses
  59141. structur
  59142. review
  59143. hosmane
  59144. narayan
  59145. frontiers
  59146. group
  59147. heter
  59148. review
  59149. hosokawa
  59150. takahiro
  59151. murahashi
  59152. aspects
  59153. review
  59154. hosoya
  59155. kumazaki
  59156. chida
  59157. ohuchi
  59158. review
  59159. hosoya
  59160. haruo
  59161. clar's
  59162. aromatic
  59163. sextet
  59164. sextet
  59165. review
  59166. initio
  59167. empirical
  59168. computations
  59169. review
  59170. kendall
  59171. tucker
  59172. dorigo
  59173. andrea
  59174. quanti
  59175. review
  59176. hounsell
  59177. elizabeth
  59178. spectroscopic
  59179. studies
  59180. compl
  59181. review
  59182. housecroft
  59183. fehlner
  59184. metalloboranes
  59185. their
  59186. review
  59187. hehre
  59188. pietro
  59189. pictorial
  59190. approa
  59191. review
  59192. yoshio
  59193. otsubo
  59194. tetsuo
  59195. ogura
  59196. fumio
  59197. review
  59198. huang
  59199. cephalotasus
  59200. alkaloids
  59201. alkaloids
  59202. review
  59203. huang
  59204. sondheimer
  59205. planar
  59206. dehydro
  59207. annulen
  59208. review
  59209. huang
  59210. arsonium
  59211. ylides
  59212. advances
  59213. review
  59214. hudlicky
  59215. reduction
  59216. organic
  59217. chemistry
  59218. ellis
  59219. review
  59220. hudlicky
  59221. milos
  59222. oxidations
  59223. organic
  59224. chemistry
  59225. review
  59226. hudlicky
  59227. kutchan
  59228. naqvi
  59229. vinylcycloprop
  59230. review
  59231. hudlicky
  59232. tomas
  59233. price
  59234. anionic
  59235. approaches
  59236. review
  59237. hudrlik
  59238. hurdlik
  59239. organosilicon
  59240. compounds
  59241. review
  59242. huenig
  59243. siegfried
  59244. aromatic/quinoid
  59245. systems
  59246. principle
  59247. review
  59248. huffman
  59249. metal
  59250. ammonia
  59251. reductions
  59252. cyclic
  59253. review
  59254. hughes
  59255. russell
  59256. organo
  59257. transition
  59258. metal
  59259. compounds
  59260. review
  59261. huisgen
  59262. steric
  59263. course
  59264. mechanism
  59265. dipolar
  59266. review
  59267. huisgen
  59268. kinetics
  59269. reaction
  59270. mechanisms
  59271. selec
  59272. review
  59273. hunig
  59274. schaller
  59275. chemistry
  59276. cyanides
  59277. review
  59278. david
  59279. michael
  59280. addition
  59281. organolithium
  59282. review
  59283. hutchins
  59284. leanr
  59285. nazer
  59286. pytlewski
  59287. pelter
  59288. review
  59289. hutchinson
  59290. biosynthetic
  59291. studies
  59292. macrolide
  59293. review
  59294. gilbert
  59295. bryant
  59296. counterattack
  59297. reagents
  59298. review
  59299. naelong
  59300. steric
  59301. influence
  59302. review
  59303. grandberg
  59304. denisov
  59305. popova
  59306. heter
  59307. review
  59308. nitta
  59309. synth
  59310. review
  59311. iacobucci
  59312. sweeny
  59313. chemistry
  59314. anthocyan
  59315. review
  59316. iddon
  59317. cycloaddition
  59318. opening
  59319. other
  59320. novel
  59321. review
  59322. ikchoon
  59323. stereoelectronic
  59324. origins
  59325. intrins
  59326. review
  59327. ikeda
  59328. masazumi
  59329. tatsunori
  59330. ishibashi
  59331. hiroyuki
  59332. review
  59333. illuminati
  59334. stegel
  59335. formation
  59336. anionic
  59337. review
  59338. imamoto
  59339. tsuneo
  59340. carbonyl
  59341. addition
  59342. reactions
  59343. promoted
  59344. review
  59345. imamoto
  59346. tsuneo
  59347. synthetic
  59348. methods
  59349. lanthanid
  59350. review
  59351. inanaga
  59352. junji
  59353. reduction
  59354. organic
  59355. functions
  59356. review
  59357. formation
  59358. convenient
  59359. chiral
  59360. intermediat
  59361. review
  59362. ingham
  59363. naturally
  59364. occurring
  59365. isoflavonoids
  59366. review
  59367. ingold
  59368. lusztyk
  59369. raner
  59370. unusual
  59371. review
  59372. ingold
  59373. walton
  59374. probing
  59375. conformations
  59376. review
  59377. ingold
  59378. keith
  59379. organic
  59380. chemistry/bioscience
  59381. review
  59382. inoue
  59383. gokel
  59384. cation
  59385. binding
  59386. macrocycles
  59387. review
  59388. inouye
  59389. reductions
  59390. chiral
  59391. dihydr
  59392. review
  59393. inubushi
  59394. ibuka
  59395. syntheses
  59396. azaspiro
  59397. review
  59398. ireland
  59399. synthetic
  59400. methodology
  59401. context
  59402. review
  59403. isaacs
  59404. effects
  59405. pressure
  59406. kinetic
  59407. isoto
  59408. review
  59409. ishii
  59410. yasutaka
  59411. ogawa
  59412. masaya
  59413. hydrogen
  59414. peroxide
  59415. oxida
  59416. review
  59417. isobe
  59418. minoru
  59419. nishikawa
  59420. toshio
  59421. herunsalee
  59422. angkana
  59423. review
  59424. isothiocyanates
  59425. chemistry
  59426. heterocycles
  59427. review
  59428. masayoshi
  59429. recent
  59430. progress
  59431. synthesis
  59432. review
  59433. fujise
  59434. fukazawa
  59435. benzenoid
  59436. phanes
  59437. review
  59438. yoshihiko
  59439. metalation
  59440. synthetic
  59441. applicat
  59442. review
  59443. olefin
  59444. metathesis
  59445. academic
  59446. press
  59447. review
  59448. iwamura
  59449. hiizu
  59450. organic
  59451. molecules
  59452. review
  59453. iwamura
  59454. hiizu
  59455. spinpolycarbenes
  59456. inpursuit
  59457. review
  59458. izumi
  59459. modified
  59460. raney
  59461. nickel
  59462. catalyst
  59463. heterog
  59464. review
  59465. chudek
  59466. foster
  59467. review
  59468. keister
  59469. organomet
  59470. ruthenium
  59471. review
  59472. chanet
  59473. vessiere
  59474. proced
  59475. review
  59476. dubac
  59477. laporterie
  59478. review
  59479. dunogues
  59480. colloquium
  59481. review
  59482. jackson
  59483. tetrahedron
  59484. reaction
  59485. review
  59486. saavedra
  59487. proced
  59488. recent
  59489. review
  59490. normant
  59491. wakselman
  59492. review
  59493. fluorine
  59494. synposium
  59495. proceedings
  59496. review
  59497. setsune
  59498. dolphin
  59499. review
  59500. mccullough
  59501. photoadditions
  59502. review
  59503. kessler
  59504. conformation
  59505. biological
  59506. activity
  59507. review
  59508. charlton
  59509. alauddin
  59510. tetrahedron
  59511. review
  59512. courtneidge
  59513. davies
  59514. review
  59515. liebscher
  59516. knoll
  59517. abegas
  59518. review
  59519. lindley
  59520. mason
  59521. sonoche
  59522. review
  59523. bobbitt
  59524. bourque
  59525. heterocycles
  59526. review
  59527. brown
  59528. angew
  59529. direct
  59530. review
  59531. o'connor
  59532. casey
  59533. review
  59534. mattay
  59535. angew
  59536. charge
  59537. review
  59538. kutney
  59539. heterocycles
  59540. studies
  59541. review
  59542. sandhu
  59543. heterocycles
  59544. review
  59545. mague
  59546. organomet
  59547. cobalt
  59548. rhodi
  59549. review
  59550. mague
  59551. organomet
  59552. cobalt
  59553. rhodi
  59554. review
  59555. welch
  59556. tetrahedron
  59557. tetrahedron
  59558. review
  59559. tsuji
  59560. minami
  59561. review
  59562. tsuji
  59563. heterocycles
  59564. contributions
  59565. review
  59566. huffman
  59567. tetrahedron
  59568. symposia
  59569. review
  59570. jache
  59571. inorganic
  59572. chemistry
  59573. hydrogen
  59574. fluor
  59575. review
  59576. jacob
  59577. juergen
  59578. sulfur
  59579. analogs
  59580. polycyclic
  59581. aromatic
  59582. review
  59583. jacobs
  59584. burke
  59585. oxazole
  59586. alkaloids
  59587. alkaloid
  59588. review
  59589. jaenicke
  59590. boland
  59591. signal
  59592. substances
  59593. their
  59594. review
  59595. james
  59596. hough
  59597. sucrose
  59598. derivative
  59599. review
  59600. janzen
  59601. edward
  59602. haire
  59603. larry
  59604. decades
  59605. review
  59606. jarvis
  59607. mazzola
  59608. macrocyclic
  59609. other
  59610. novel
  59611. review
  59612. jencks
  59613. reaction
  59614. choose
  59615. mechanism
  59616. review
  59617. jenks
  59618. turro
  59619. exchange
  59620. effects
  59621. cidep
  59622. review
  59623. jiang
  59624. xikui
  59625. polyfluorinated
  59626. nitroxides
  59627. review
  59628. mague
  59629. organomet
  59630. cobalt
  59631. rhodi
  59632. review
  59633. jiang
  59634. novel
  59635. pathways
  59636. electron
  59637. transfer
  59638. review
  59639. jones
  59640. crystal
  59641. structure
  59642. determination
  59643. critica@
  59644. review
  59645. jutzi
  59646. peter
  59647. group
  59648. metallocenes
  59649. recent
  59650. developm@
  59651. review
  59652. kaden
  59653. synthesis
  59654. metal
  59655. complexes
  59656. azamacro@
  59657. review
  59658. kametani
  59659. koizumi
  59660. phenethylisoquinolin
  59661. alkaloids@
  59662. review
  59663. karnojitzky
  59664. oxidation
  59665. ketones
  59666. molecular
  59667. review
  59668. kauffmann
  59669. possible
  59670. applications
  59671. heavy
  59672. main@
  59673. review
  59674. khenkin
  59675. shilov
  59676. biomimetic
  59677. alkane
  59678. oxidation
  59679. review
  59680. kishi
  59681. chemical
  59682. synthesis
  59683. polyether
  59684. antibiotics
  59685. review
  59686. knowles
  59687. jeremy
  59688. mechanistic
  59689. ingenuity
  59690. enzyme
  59691. review
  59692. kolodyazhnyi
  59693. kukhar
  59694. hetero
  59695. substituted
  59696. review
  59697. kotali
  59698. antigoni
  59699. tsoungas
  59700. petros
  59701. pyrazole
  59702. oxides@
  59703. review
  59704. krief
  59705. dumont
  59706. halazy
  59707. labar
  59708. laboureur
  59709. review
  59710. jiang
  59711. novel
  59712. pathways
  59713. electron
  59714. transfer
  59715. review
  59716. johansen
  59717. enzymatic
  59718. synthesis
  59719. peptides
  59720. review
  59721. peter
  59722. sachs
  59723. horst
  59724. calculating
  59725. numbers
  59726. review
  59727. johnson
  59728. barbachyn
  59729. optical
  59730. activation
  59731. review
  59732. johnson
  59733. richard
  59734. cyclic
  59735. cumulenes
  59736. advances
  59737. review
  59738. johnson
  59739. richard
  59740. strained
  59741. cyclic
  59742. cumulenes
  59743. review
  59744. johnston
  59745. scaiano
  59746. resolved
  59747. studies
  59748. review
  59749. jolley
  59750. bradshaw
  59751. izatt
  59752. synthetic
  59753. chiral
  59754. review
  59755. jonas
  59756. klaus
  59757. findings
  59758. arene
  59759. chemistry
  59760. review
  59761. jones
  59762. bradshaw
  59763. synthesis
  59764. reduction
  59765. review
  59766. jones
  59767. aromatic
  59768. quinolizines
  59769. advances
  59770. review
  59771. jones
  59772. quinoline
  59773. oxides
  59774. chemistry
  59775. review
  59776. jones
  59777. sliskovic
  59778. chemistry
  59779. triazolo
  59780. review
  59781. jones
  59782. gurnos
  59783. greenhill
  59784. quinolines
  59785. review
  59786. jones
  59787. taylor
  59788. isotopic
  59789. hydrogen
  59790. exchange
  59791. review
  59792. jones
  59793. crystal
  59794. structure
  59795. determination
  59796. critica
  59797. review
  59798. jones
  59799. pyrroles
  59800. synthesis
  59801. review
  59802. jones
  59803. pyrroles
  59804. synthesis
  59805. review
  59806. jones
  59807. william
  59808. feher
  59809. frank
  59810. comparative
  59811. reactivit
  59812. review
  59813. jordan
  59814. richard
  59815. bradley
  59816. prudence
  59817. lapointe
  59818. robert
  59819. review
  59820. jorgensen
  59821. william
  59822. energy
  59823. calculations
  59824. review
  59825. jorgensen
  59826. william
  59827. laird
  59828. ellen
  59829. gushurst
  59830. review
  59831. joule
  59832. recent
  59833. advances
  59834. chemistry
  59835. review
  59836. joule
  59837. thianthrenes
  59838. advances
  59839. review
  59840. juaristi
  59841. eusebio
  59842. conformational
  59843. analysis
  59844. review
  59845. juaristi
  59846. eusebio
  59847. recent
  59848. studies
  59849. anomeric
  59850. review
  59851. juaristi
  59852. eusebio
  59853. second
  59854. anomeric
  59855. interactions
  59856. review
  59857. junjappa
  59858. asokan
  59859. oxoketene
  59860. review
  59861. jurczak
  59862. baranowski
  59863. editors
  59864. pressure
  59865. chemic
  59866. review
  59867. jurczak
  59868. janusz
  59869. golebiowski
  59870. optically
  59871. active
  59872. review
  59873. jutzi
  59874. peter
  59875. group
  59876. metallocenes
  59877. recent
  59878. developm
  59879. review
  59880. jutzi
  59881. peter
  59882. coordination
  59883. group
  59884. elements
  59885. review
  59886. furuhashi
  59887. synth
  59888. produc
  59889. review
  59890. nicholas
  59891. chemistry
  59892. review
  59893. smith
  59894. cavaleiro
  59895. heterocycles
  59896. review
  59897. mullen
  59898. angew
  59899. review
  59900. senga
  59901. synth
  59902. synthesis
  59903. review
  59904. smith
  59905. london
  59906. advances
  59907. organo
  59908. review
  59909. tanaka
  59910. mitsuhashi
  59911. synth
  59912. review
  59913. troev
  59914. borisov
  59915. phosphorus
  59916. sulphur
  59917. review
  59918. utimoto
  59919. synth
  59920. organic
  59921. review
  59922. kabalka
  59923. incorporation
  59924. stable
  59925. radioactive
  59926. review
  59927. kabalka
  59928. george
  59929. varma
  59930. rajender
  59931. synthesis
  59932. review
  59933. kabbe
  59934. widdig
  59935. synthesis
  59936. reactions
  59937. review
  59938. kadaba
  59939. pankaja
  59940. triazolines
  59941. 46169
  59942. review
  59943. kaden
  59944. synthesis
  59945. metal
  59946. complexes
  59947. azamacro
  59948. review
  59949. kadish
  59950. xihai
  59951. anderson
  59952. james
  59953. recommended
  59954. review
  59955. kadryov
  59956. rokhlin
  59957. fluoralkenylphosphon
  59958. review
  59959. kaesz
  59960. ziling
  59961. yeajer
  59962. knobler
  59963. carolyn
  59964. review
  59965. kagan
  59966. divalent
  59967. samarium
  59968. compounds
  59969. perspectives
  59970. review
  59971. kagan
  59972. fiaud
  59973. kinetic
  59974. resolution
  59975. 198818
  59976. review
  59977. kagan
  59978. henri
  59979. asymmetric
  59980. catalysis
  59981. organic
  59982. synth
  59983. review
  59984. kagan
  59985. henri
  59986. sasaki
  59987. mitsuru
  59988. collin
  59989. jacqueline
  59990. review
  59991. versatile
  59992. chemistry
  59993. diazines
  59994. organ
  59995. review
  59996. kaiser
  59997. synthetic
  59998. approaches
  59999. biologically
  60000. review
  60001. kaiser
  60002. thomas
  60003. mihara
  60004. hisakazu
  60005. laforet
  60006. geneviev
  60007. review
  60008. kaitmazova
  60009. gambaryan
  60010. rokhlin
  60011. amines
  60012. review
  60013. kamal
  60014. ahmed
  60015. recent
  60016. advances
  60017. synthetic
  60018. review
  60019. kamernitskii
  60020. turuta
  60021. reactivity
  60022. conforma
  60023. review
  60024. kametani
  60025. fukumoto
  60026. ihara
  60027. synthesis
  60028. carbapen
  60029. review
  60030. kametani
  60031. koizumi
  60032. phenethylisoquinolin
  60033. alkaloids
  60034. review
  60035. kamigata
  60036. nobumasa
  60037. shimizu
  60038. toshio
  60039. synthesis
  60040. stereoch
  60041. review
  60042. kamiya
  60043. nocardicins
  60044. chemistry
  60045. review
  60046. kammer
  60047. lactam
  60048. antibiotics
  60049. clinical
  60050. medicin
  60051. review
  60052. kanamori
  60053. roberts
  60054. studies
  60055. biologica
  60056. review
  60057. maguire
  60058. honig
  60059. sweigart
  60060. nucleophi
  60061. review
  60062. singh
  60063. martin
  60064. doyle
  60065. chemistry
  60066. review
  60067. kaneko
  60068. naito
  60069. syntheses
  60070. reactions
  60071. cyclobu
  60072. review
  60073. kanemasa
  60074. shuji
  60075. tsuge
  60076. otohiko
  60077. recent
  60078. advances
  60079. review
  60080. angray
  60081. kingsbury
  60082. gillian
  60083. blackburn
  60084. micha
  60085. review
  60086. kanner
  60087. butylpyridine
  60088. unusual
  60089. review
  60090. kanner
  60091. organofluorosilanes
  60092. silicon
  60093. compounds
  60094. review
  60095. kaplan
  60096. radicals
  60097. reactive
  60098. intermediates
  60099. review
  60100. karaev
  60101. goraeva
  60102. sladkov
  60103. propargyl
  60104. compo
  60105. review
  60106. karle
  60107. elucidation
  60108. structural
  60109. formula
  60110. configu
  60111. review
  60112. karnojitzky
  60113. oxidation
  60114. ketones
  60115. molecular
  60116. review
  60117. karpyshev
  60118. phosphite
  60119. synthesis
  60120. oligodeoxyribo
  60121. review
  60122. rauch
  60123. labeled
  60124. proteins
  60125. their
  60126. preparation
  60127. review
  60128. kashin
  60129. keletskaya
  60130. oxidation
  60131. organometall
  60132. review
  60133. kashman
  60134. carmely
  60135. blasberger
  60136. hirsch
  60137. green
  60138. review
  60139. katawala
  60140. coppola
  60141. schuster
  60142. herbert
  60143. review
  60144. shinzi
  60145. ishida
  60146. masaru
  60147. acyclic
  60148. dithiocarboxylic
  60149. review
  60150. katritzky
  60151. sengupta
  60152. rewcastle
  60153. review
  60154. katritzky
  60155. marson
  60156. pyrilium
  60157. mediated
  60158. transfor
  60159. review
  60160. katritzky
  60161. musumarra
  60162. insights
  60163. aliphat
  60164. review
  60165. katritzky
  60166. brycki
  60167. bogumil
  60168. nucleophilic
  60169. review
  60170. katritzky
  60171. brycki
  60172. bogumil
  60173. mechanisms
  60174. review
  60175. katritzky
  60176. dennis
  60177. nicholas
  60178. cycloaddition
  60179. review
  60180. katritzky
  60181. savage
  60182. sensor
  60183. coatings
  60184. review
  60185. katritzky
  60186. taylor
  60187. roger
  60188. electrophilic
  60189. substit
  60190. review
  60191. kauffmann
  60192. possible
  60193. applications
  60194. heavy
  60195. review
  60196. kaufmann
  60197. dieter
  60198. schacht
  60199. wolfgang
  60200. benzannelated
  60201. review
  60202. kaupp
  60203. complex
  60204. eliminations
  60205. eliminations
  60206. review
  60207. kawada
  60208. kenji
  60209. moonsun
  60210. david
  60211. synthesis
  60212. review
  60213. kazanskii
  60214. modern
  60215. ideas
  60216. about
  60217. mechanism
  60218. review
  60219. keefer
  60220. larry
  60221. george
  60222. nickel
  60223. aluminum
  60224. alloy
  60225. review
  60226. keehn
  60227. crystal
  60228. structure
  60229. cyclophanes
  60230. cyclophane
  60231. review
  60232. keinan
  60233. doron
  60234. total
  60235. synthesis
  60236. polypreno
  60237. review
  60238. keinan
  60239. silicon
  60240. hydrides
  60241. organic
  60242. synthesis
  60243. review
  60244. kellogg
  60245. bioorganic
  60246. modelling
  60247. stereoselective
  60248. review
  60249. kellogg
  60250. chiral
  60251. macrocycles
  60252. reagents
  60253. review
  60254. kennedy
  60255. marechal
  60256. carbocationic
  60257. polymerization
  60258. review
  60259. kerber
  60260. complexes
  60261. trienes
  60262. tetraenes
  60263. review
  60264. kerridge
  60265. chemistry
  60266. molten
  60267. acetamide
  60268. review
  60269. khardin
  60270. radchenko
  60271. polymeric
  60272. derivatives
  60273. review
  60274. khenkin
  60275. shilov
  60276. biomimetic
  60277. alkane
  60278. oxidation
  60279. review
  60280. khramtsov
  60281. vainer
  60282. photon
  60283. transfer
  60284. reactions
  60285. review
  60286. khripsch
  60287. synthesis
  60288. brassinosteroids
  60289. review
  60290. kibayashi
  60291. chihairo
  60292. stereocontrolled
  60293. nucleophilic
  60294. review
  60295. kichoom
  60296. bekkum
  60297. aspects
  60298. chemical
  60299. review
  60300. kyoung
  60301. activation
  60302. superoxid
  60303. review
  60304. kimura
  60305. eiichi
  60306. developments
  60307. functionalization
  60308. review
  60309. khemani
  60310. skonieczny
  60311. payne
  60312. sulfony
  60313. review
  60314. arene
  60315. complexes
  60316. organic
  60317. chemistr
  60318. review
  60319. steven
  60320. miller
  60321. anthony
  60322. schwar
  60323. review
  60324. kirby
  60325. stereoelectronic
  60326. effects
  60327. acetal
  60328. hydrol
  60329. review
  60330. kirby
  60331. anomeric
  60332. effect
  60333. related
  60334. stereoele
  60335. review
  60336. kirsh
  60337. smsov
  60338. popkov
  60339. timashev
  60340. perfl
  60341. review
  60342. kiselev
  60343. konovalov
  60344. factors
  60345. determine
  60346. review
  60347. kishi
  60348. chemical
  60349. synthesis
  60350. polyether
  60351. antibiotics
  60352. review
  60353. kishi
  60354. chemical
  60355. synthesis
  60356. polyether
  60357. antibiotics
  60358. review
  60359. kishi
  60360. yoshito
  60361. natural
  60362. products
  60363. synthesis
  60364. palytoxin
  60365. review
  60366. klabunovskii
  60367. advances
  60368. enantioselective
  60369. hydro
  60370. review
  60371. klarner
  60372. rearrangements
  60373. systems
  60374. review
  60375. klaui
  60376. wolfgang
  60377. coordination
  60378. chemistry
  60379. organ
  60380. review
  60381. klein
  60382. douglas
  60383. semiempirical
  60384. valence
  60385. views
  60386. review
  60387. klein
  60388. directive
  60389. effects
  60390. allylic
  60391. benzylic
  60392. review
  60393. kleinschroth
  60394. chemical
  60395. behavior
  60396. review
  60397. klemm
  60398. syntheses
  60399. tetracyclic
  60400. pentacyclic
  60401. review
  60402. klemm
  60403. leroy
  60404. interrelationships
  60405. among
  60406. condens
  60407. review
  60408. klibanov
  60409. alexander
  60410. asymmetric
  60411. transformations
  60412. review
  60413. klumpp
  60414. reactivity
  60415. organic
  60416. chemistry
  60417. wiley
  60418. review
  60419. klunder
  60420. zwanenburg
  60421. strained
  60422. bridgehead
  60423. review
  60424. knauth
  60425. saobah
  60426. thernlochemistry
  60427. organic
  60428. compo
  60429. review
  60430. knirel
  60431. yuriy
  60432. vinogradov
  60433. evgeny
  60434. andrew
  60435. review
  60436. knowles
  60437. jeremy
  60438. mechanistic
  60439. ingenuity
  60440. enzyme
  60441. review
  60442. knowles
  60443. asymmetric
  60444. hydrogenation
  60445. 198316
  60446. review
  60447. knunyants
  60448. sizov
  60449. ukharov
  60450. synthesis
  60451. review
  60452. kobayashi
  60453. kumadaki
  60454. dewar
  60455. heterocycles
  60456. relat
  60457. review
  60458. kober
  60459. aminoarsanes
  60460. preparative
  60461. reagents
  60462. review
  60463. kratochvil
  60464. kvasnicka
  60465. matyska
  60466. pospichal
  60467. review
  60468. partitioning
  60469. carbanion
  60470. interme
  60471. review
  60472. kochetkov
  60473. microbial
  60474. polysaccharides
  60475. approac
  60476. review
  60477. kochi
  60478. radical
  60479. cations
  60480. reactive
  60481. intermediates
  60482. review
  60483. kochi
  60484. charge
  60485. transfer
  60486. excitation
  60487. molecular
  60488. review
  60489. koester
  60490. roland
  60491. yalpani
  60492. mohamed
  60493. outline
  60494. review
  60495. reductions
  60496. using
  60497. hydrosilanes
  60498. silicon
  60499. review
  60500. michael
  60501. ketene
  60502. dithioacetals
  60503. organic
  60504. synthe
  60505. review
  60506. kolbanovskii
  60507. method
  60508. adiabatic
  60509. compressi
  60510. review
  60511. kolesov
  60512. papina
  60513. thermochemistry
  60514. haloethan
  60515. review
  60516. kolodyazhnyi
  60517. kukhar
  60518. hetero
  60519. substituted
  60520. review
  60521. konovalov
  60522. reactivity
  60523. addends
  60524. review
  60525. kopecky
  60526. synthesis
  60527. dioxetanes
  60528. chemical
  60529. review
  60530. koppel
  60531. synthesis
  60532. lactam
  60533. function
  60534. review
  60535. koptyug
  60536. contemporary
  60537. problems
  60538. carbonium
  60539. review
  60540. kornblum
  60541. nathan
  60542. synthetic
  60543. aspects
  60544. electron
  60545. trans
  60546. review
  60547. korneeva
  60548. lokteev
  60549. synthesis
  60550. ethylene
  60551. review
  60552. korshak
  60553. rusanov
  60554. phenyl
  60555. substituted
  60556. polyhete
  60557. review
  60558. korshak
  60559. rusanov
  60560. tugushi
  60561. reductive
  60562. polyh
  60563. review
  60564. koskinen
  60565. lounasmaa
  60566. sarpagin
  60567. ajmaline
  60568. group
  60569. review
  60570. kosower
  60571. intramolecular
  60572. donor
  60573. acceptor
  60574. systems
  60575. review
  60576. kosower
  60577. stable
  60578. pyridinyl
  60579. radicals
  60580. 1983112
  60581. topic
  60582. review
  60583. koster
  60584. cimarusti
  60585. sykes
  60586. monobactams
  60587. review
  60588. kostikov
  60589. molchanov
  60590. dihalocyclopr
  60591. review
  60592. kostikov
  60593. molchanov
  60594. khlebnikov
  60595. halogen
  60596. review
  60597. kotali
  60598. antigoni
  60599. tsoungas
  60600. petros
  60601. pyrazole
  60602. oxides
  60603. review
  60604. koval
  60605. advances
  60606. chemistry
  60607. sulphenic
  60608. review
  60609. kozhevnikov
  60610. mechanism
  60611. oxidative
  60612. review
  60613. kozhushko
  60614. lomakina
  60615. shokol
  60616. phosphorus
  60617. review
  60618. kozikowski
  60619. isoxazoline
  60620. route
  60621. molecul
  60622. review
  60623. kozina
  60624. mastryukov
  60625. mil'vitskaya
  60626. review
  60627. krakowiak
  60628. krzysztof
  60629. bradshaw
  60630. jerald
  60631. zamecka
  60632. review
  60633. kramer
  60634. george
  60635. scouten
  60636. charles
  60637. norbornyl
  60638. review
  60639. krapcho
  60640. synthetic
  60641. applications
  60642. dealkoxycarbo
  60643. review
  60644. krasovitskii
  60645. bolotin
  60646. organic
  60647. luminescent
  60648. review
  60649. kraus
  60650. george
  60651. thomas
  60652. laramay
  60653. steve
  60654. review
  60655. krechl
  60656. castulik
  60657. pavel
  60658. enzyme
  60659. models
  60660. based
  60661. review
  60662. kreissl
  60663. metal
  60664. complexes
  60665. carbene
  60666. complexes
  60667. review
  60668. kresge
  60669. jerry
  60670. flash
  60671. photolytic
  60672. generation
  60673. review
  60674. krief
  60675. dumont
  60676. halazy
  60677. labar
  60678. laboureur
  60679. review
  60680. krief
  60681. dumont
  60682. halazy
  60683. labar
  60684. laboureur
  60685. review
  60686. krief
  60687. hevesi
  60688. organoselenium
  60689. chemistry
  60690. functio
  60691. review
  60692. krief
  60693. laboureur
  60694. dumont
  60695. labar
  60696. transformati
  60697. review
  60698. krivdin
  60699. kalabin
  60700. structural
  60701. applications
  60702. review
  60703. krogh
  60704. photoinduced
  60705. electron
  60706. transfer
  60707. review
  60708. krohn
  60709. building
  60710. blocks
  60711. total
  60712. synthesis
  60713. review
  60714. krohn
  60715. synthesis
  60716. anthracyclinones
  60717. electrophi
  60718. review
  60719. tsvetkov
  60720. neutral
  60721. acyclic
  60722. analogues
  60723. review
  60724. kropp
  60725. photobehavior
  60726. alkyl
  60727. halides
  60728. solutio
  60729. review
  60730. kroto
  60731. harold
  60732. fullerenes
  60733. giant
  60734. fullerenes
  60735. review
  60736. kroto
  60737. harold
  60738. giant
  60739. fullerenes
  60740. chemis
  60741. review
  60742. kroto
  60743. harold
  60744. space
  60745. stars
  60746. review
  60747. krstulovic
  60748. brown
  60749. reversed
  60750. phase
  60751. perfor
  60752. review
  60753. krstulovic
  60754. chiral
  60755. separations
  60756. ellis
  60757. review
  60758. krygowski
  60759. tadeusz
  60760. marek
  60761. correlation
  60762. analysis
  60763. review
  60764. kuczkowski
  60765. formation
  60766. structures
  60767. ozonides
  60768. review
  60769. kuehne
  60770. martin
  60771. marko
  60772. istvan
  60773. syntheses
  60774. vinblasti
  60775. review
  60776. kukhar
  60777. yagupol'skii
  60778. soloshonok
  60779. fluor
  60780. review
  60781. kukolja
  60782. chauvette
  60783. cephalosporin
  60784. antibiotics
  60785. review
  60786. kulinkovich
  60787. carbene
  60788. methods
  60789. introductio
  60790. review
  60791. kulkarni
  60792. yashwamt
  60793. carboxyolefination
  60794. 199023
  60795. review
  60796. kurzer
  60797. thiadiazoles
  60798. advances
  60799. review
  60800. kuthan
  60801. pyrans
  60802. thiopyrans
  60803. selenopyrans
  60804. review
  60805. kutney
  60806. turnbull
  60807. compounds
  60808. containing
  60809. review
  60810. kuwajima
  60811. nakamura
  60812. metal
  60813. homoenolates
  60814. silox
  60815. review
  60816. kuwajima
  60817. alkoxy
  60818. siloxycyclopropanes
  60819. review
  60820. kuznetsov
  60821. zefirov
  60822. azaadamantanes
  60823. nitro
  60824. review
  60825. kuznetsov
  60826. evgenii
  60827. shcherbakova
  60828. irina
  60829. balaban
  60830. review
  60831. kuznetsov
  60832. ioffe
  60833. present
  60834. state
  60835. review
  60836. kwart
  60837. temperature
  60838. dependence
  60839. primary
  60840. kinet
  60841. review
  60842. kuczkowski
  60843. formation
  60844. structures
  60845. ozonides@
  60846. review
  60847. carpino
  60848. fluoroen@
  60849. review
  60850. lamare
  60851. veronique
  60852. furstoss
  60853. roland
  60854. bioconversion
  60855. review
  60856. laszlo
  60857. pierre
  60858. catalysis
  60859. organic
  60860. reactions
  60861. review
  60862. marie
  60863. perspectives
  60864. supramolecular
  60865. chem@
  60866. review
  60867. electron
  60868. spectroscopy
  60869. organic
  60870. review
  60871. lloyd
  60872. david
  60873. goodall
  60874. david
  60875. polarimetric
  60876. detectio@
  60877. review
  60878. wolfgang
  60879. keese
  60880. reinhart
  60881. strained
  60882. olefins
  60883. struc@
  60884. review
  60885. polarimetry
  60886. asymmetric
  60887. synthesis
  60888. review
  60889. ramaiah
  60890. tetrahedron
  60891. radical
  60892. reaction@
  60893. review
  60894. majetich
  60895. george
  60896. allylsilanes
  60897. organic
  60898. synthesis
  60899. review
  60900. manuilov
  60901. barkhash
  60902. recent
  60903. trends
  60904. theo@
  60905. review
  60906. markovskii
  60907. pashinnik
  60908. fluorination
  60909. organi@
  60910. review
  60911. masamune
  60912. satoru
  60913. asymmetric
  60914. synthesis
  60915. applic@
  60916. review
  60917. carpino
  60918. fluoroen
  60919. review
  60920. pavlova
  60921. alkyl
  60922. review
  60923. freedman
  60924. organomet
  60925. review
  60926. freedman
  60927. freeman
  60928. review
  60929. eberson
  60930. radner
  60931. review
  60932. belen'kii
  60933. heterocycl
  60934. compd
  60935. effect
  60936. review
  60937. yagupolskii
  60938. fluor
  60939. aromatic
  60940. review
  60941. brezhnev
  60942. vartanyan
  60943. solov'eva
  60944. zetiro
  60945. review
  60946. l'abbe
  60947. trnnsformation
  60948. renations
  60949. review
  60950. laarhoven
  60951. photochemical
  60952. cyclizations
  60953. intram
  60954. review
  60955. laarhoven
  60956. photocyclizations
  60957. intramolecula
  60958. review
  60959. labeish
  60960. petrov
  60961. reactions
  60962. involving
  60963. review
  60964. labia
  60965. morin
  60966. stereospecific
  60967. constructions
  60968. review
  60969. laird
  60970. trevor
  60971. neglected
  60972. science
  60973. chemical
  60974. review
  60975. lamare
  60976. veronique
  60977. furstoss
  60978. roland
  60979. bioconversion
  60980. review
  60981. lamare
  60982. veronique
  60983. furstoss
  60984. roland
  60985. bioconversion
  60986. review
  60987. lambert
  60988. joseph
  60989. interaction
  60990. silicon
  60991. review
  60992. lammertsma
  60993. schleyer
  60994. schwarz
  60995. helmut
  60996. review
  60997. landor
  60998. experimental
  60999. techniques
  61000. chemistry
  61001. review
  61002. landor
  61003. synthesis
  61004. allenes
  61005. conjugated
  61006. review
  61007. landor
  61008. jacobs
  61009. reactions
  61010. allenes
  61011. review
  61012. landor
  61013. naturally
  61014. occurring
  61015. allenes
  61016. chemistr
  61017. review
  61018. lapachev
  61019. pebrenko
  61020. mamaev
  61021. azinyl
  61022. review
  61023. lapidus
  61024. pirozhkov
  61025. catalytic
  61026. synthesis
  61027. review
  61028. larock
  61029. organometallic
  61030. approaches
  61031. heteroc
  61032. review
  61033. larock
  61034. organomercurials
  61035. organic
  61036. synthesis
  61037. review
  61038. larock
  61039. richard
  61040. comprehensive
  61041. organic
  61042. transformati
  61043. review
  61044. larock
  61045. richard
  61046. applications
  61047. organopalladiu
  61048. review
  61049. larson
  61050. silyl
  61051. carbonyl
  61052. compounds
  61053. synthesis
  61054. review
  61055. larson
  61056. introduction
  61057. organosilicon
  61058. chemist
  61059. review
  61060. laszlo
  61061. pierre
  61062. catalysis
  61063. organic
  61064. reactions
  61065. review
  61066. laszlo
  61067. pierre
  61068. cornelis
  61069. andre
  61070. supported
  61071. cupric
  61072. review
  61073. launer
  61074. infrared
  61075. analysis
  61076. organosilicon
  61077. compo
  61078. review
  61079. lazar
  61080. milan
  61081. rychly
  61082. jozef
  61083. klimo
  61084. viliam
  61085. pelikan
  61086. peter
  61087. review
  61088. noble
  61089. organic
  61090. pressure
  61091. chemistry
  61092. review
  61093. lebozec
  61094. hubert
  61095. touchard
  61096. daniel
  61097. dixneuf
  61098. pierre
  61099. review
  61100. franz
  61101. schleicher
  61102. erwin
  61103. aspects
  61104. review
  61105. lednicer
  61106. mitscher
  61107. organic
  61108. chemistry
  61109. review
  61110. lednicer
  61111. daniel
  61112. mitscher
  61113. lester
  61114. georg
  61115. gunda
  61116. review
  61117. phase
  61118. transfer
  61119. assisted
  61120. permanganate
  61121. oxidat
  61122. review
  61123. ikchoon
  61124. characterization
  61125. transition
  61126. states
  61127. review
  61128. synthesis
  61129. azaphenalenes
  61130. review
  61131. leffler
  61132. grunwald
  61133. ernest
  61134. rates
  61135. equilibria
  61136. review
  61137. legler
  61138. gunther
  61139. glycoside
  61140. hydrolases
  61141. mechanistic
  61142. review
  61143. lehmkuhl
  61144. herbert
  61145. specific
  61146. reactions
  61147. organylmetal
  61148. review
  61149. marie
  61150. perspectives
  61151. supramolecular
  61152. review
  61153. xuegong
  61154. reactions
  61155. triplet
  61156. benzyl
  61157. radical
  61158. review
  61159. lemmen
  61160. peter
  61161. baumgartner
  61162. regina
  61163. ramirez
  61164. review
  61165. lenoir
  61166. dieter
  61167. application
  61168. valent
  61169. titaniu
  61170. review
  61171. leonard
  61172. dimensional
  61173. probes
  61174. enzyme
  61175. coenzyme
  61176. review
  61177. lerner
  61178. richard
  61179. benkovic
  61180. stephen
  61181. observations
  61182. review
  61183. leuenberger
  61184. interrelations
  61185. chemistry
  61186. review
  61187. levin
  61188. arynes
  61189. reactive
  61190. intermediates
  61191. volume
  61192. review
  61193. lewars
  61194. oxirenes
  61195. chemical
  61196. reviews
  61197. review
  61198. lewis
  61199. edward
  61200. equilibrium
  61201. characterizati
  61202. review
  61203. steve
  61204. caroline
  61205. ultrasound
  61206. synthesi
  61207. review
  61208. steven
  61209. toogood
  61210. peter
  61211. insect
  61212. antifeedants
  61213. review
  61214. liebman
  61215. fluorine
  61216. chemistry
  61217. without
  61218. fluorine
  61219. review
  61220. liebman
  61221. conceptual
  61222. chemistry
  61223. cyclophanes
  61224. review
  61225. lightner
  61226. mcdonagh
  61227. molecular
  61228. mechanisms
  61229. review
  61230. electron
  61231. spectroscopy
  61232. organic
  61233. review
  61234. lindberg
  61235. structural
  61236. studies
  61237. polysaccharides
  61238. review
  61239. lindberg
  61240. bengt
  61241. components
  61242. bacterial
  61243. polysacchari
  61244. review
  61245. lindberg
  61246. strategies
  61247. tactics
  61248. organic
  61249. review
  61250. lindberg
  61251. thomas
  61252. strategies
  61253. tactics
  61254. organi
  61255. review
  61256. lindley
  61257. copper
  61258. assisted
  61259. nucleophilic
  61260. substitution
  61261. review
  61262. liotta
  61263. volmer
  61264. organic
  61265. syntheses
  61266. reaction
  61267. review
  61268. liotta
  61269. organoselenium
  61270. methodology
  61271. 198417
  61272. review
  61273. lipczynska
  61274. kochany
  61275. aspects
  61276. hydroxam
  61277. review
  61278. lipscomb
  61279. acceleration
  61280. reactions
  61281. enzymes
  61282. review
  61283. lipshutz
  61284. wilhelm
  61285. kozlowski
  61286. chemistr
  61287. review
  61288. thermolysis
  61289. photolysis
  61290. diaziri
  61291. review
  61292. asato
  61293. photochemistry
  61294. synthesis
  61295. review
  61296. gelsemium
  61297. alkaloids
  61298. alkaloids
  61299. review
  61300. lloyd
  61301. benzenoid
  61302. conjugated
  61303. carbocyclic
  61304. compou
  61305. review
  61306. lloyd
  61307. david
  61308. goodall
  61309. david
  61310. polarimetric
  61311. detectio
  61312. review
  61313. lloyd
  61314. douglas
  61315. chemistry
  61316. conjugated
  61317. compou
  61318. review
  61319. loewenthal
  61320. guide
  61321. perplexed
  61322. review
  61323. lopez
  61324. photoinduced
  61325. electron
  61326. transfer
  61327. oxygenations
  61328. review
  61329. lough
  61330. chiral
  61331. liquid
  61332. chromatography
  61333. blackie
  61334. review
  61335. lounasmaa
  61336. galambos
  61337. indole
  61338. alkaloid
  61339. production
  61340. review
  61341. lounasmaa
  61342. nemes
  61343. synthesis
  61344. indole
  61345. review
  61346. lounasmaa
  61347. tropane
  61348. alkaloids
  61349. alkaloids
  61350. review
  61351. lounasman
  61352. koskinen
  61353. modified
  61354. polonovski
  61355. reaction
  61356. review
  61357. chiral
  61358. phosphate
  61359. ester
  61360. 198316
  61361. review
  61362. newer
  61363. approaches
  61364. study
  61365. mecha
  61366. review
  61367. william
  61368. synthetic
  61369. chemistry
  61370. naturally
  61371. review
  61372. lozac'h
  61373. goodson
  61374. nodal
  61375. nomenclature
  61376. specifi
  61377. review
  61378. lozac'h
  61379. forty
  61380. years
  61381. heterocyclic
  61382. sulfur
  61383. review
  61384. xiyan
  61385. reactions
  61386. valent
  61387. transition
  61388. metal
  61389. review
  61390. wolfgang
  61391. keese
  61392. reinhart
  61393. strained
  61394. olefins
  61395. struc
  61396. review
  61397. metal
  61398. carbonyl
  61399. promoted
  61400. carbon
  61401. sulfur
  61402. review
  61403. transition
  61404. metal
  61405. mediated
  61406. review
  61407. lukacs
  61408. gabor
  61409. masaji
  61410. editors
  61411. recent
  61412. progress
  61413. review
  61414. lukevics
  61415. pudova
  61416. sturkovich
  61417. molecular
  61418. structur
  61419. review
  61420. tabakovic
  61421. electrolysis
  61422. heterocyclic
  61423. review
  61424. henning
  61425. baizer
  61426. manuel
  61427. organic
  61428. spect
  61429. review
  61430. lundstrom
  61431. phenethylamines
  61432. ephedrines
  61433. review
  61434. lundstrom
  61435. simple
  61436. isoquinoline
  61437. alkaloids
  61438. alkal
  61439. review
  61440. lutomski
  61441. meyers
  61442. asymmetric
  61443. synthesis
  61444. review
  61445. catalysis
  61446. claisen
  61447. rearrang
  61448. review
  61449. luzzio
  61450. frederick
  61451. guziec
  61452. frank
  61453. recent
  61454. applica
  61455. review
  61456. lwowski
  61457. nitrenes
  61458. reactive
  61459. intermediates
  61460. review
  61461. lyapina
  61462. present
  61463. state
  61464. research
  61465. review
  61466. lyerla
  61467. yannoni
  61468. chemical
  61469. applicatio
  61470. review
  61471. polarimetry
  61472. asymmetric
  61473. synthesis
  61474. review
  61475. lyubovskaya
  61476. organic
  61477. metals
  61478. superconductors
  61479. review
  61480. parish
  61481. cyclodextrins
  61482. review
  61483. braun
  61484. angew
  61485. stereosel
  61486. review
  61487. brookhart
  61488. studabaker
  61489. review
  61490. chanon
  61491. electron
  61492. transfer
  61493. review
  61494. evers
  61495. chemica
  61496. scripta
  61497. alkane
  61498. thiolate
  61499. review
  61500. fujita
  61501. hiyama
  61502. synth
  61503. review
  61504. vinogradov
  61505. review
  61506. chisholm
  61507. cleavage
  61508. review
  61509. elnagdi
  61510. sherif
  61511. mohareb
  61512. heterocycles
  61513. review
  61514. hirobe
  61515. synth
  61516. catalytic
  61517. review
  61518. hearn
  61519. proced
  61520. review
  61521. petrov
  61522. petrov
  61523. review
  61524. makosza
  61525. winiarski
  61526. review
  61527. ramaiah
  61528. tetrahedron
  61529. radical
  61530. reaction
  61531. review
  61532. ramaiah
  61533. tetrahedron
  61534. tetrahedron
  61535. review
  61536. srebnik
  61537. ramachandran
  61538. aldrichimica
  61539. review
  61540. tanaka
  61541. synth
  61542. perspec
  61543. review
  61544. tisler
  61545. proced
  61546. synthetic
  61547. review
  61548. veith
  61549. angew
  61550. unsaturate
  61551. review
  61552. beyerman
  61553. imidazole
  61554. alkaloids
  61555. review
  61556. mackie
  61557. smith
  61558. aitken
  61559. guidebook
  61560. organi
  61561. review
  61562. macomber
  61563. rausch
  61564. functionally
  61565. subst
  61566. review
  61567. madeselaire
  61568. michel
  61569. reduction
  61570. sulfoxides
  61571. thioe
  61572. review
  61573. magnus
  61574. gallagher
  61575. brown
  61576. pappalardo
  61577. indol
  61578. review
  61579. magnusson
  61580. rearrangements
  61581. epoxy
  61582. alcohols
  61583. review
  61584. maier
  61585. gunther
  61586. unusual
  61587. molecules
  61588. unusual
  61589. reactions
  61590. review
  61591. maier
  61592. shell
  61593. organic
  61594. cations
  61595. spectroscopic
  61596. review
  61597. majectic
  61598. newkome
  61599. pyridinophanes
  61600. pyridinocro
  61601. review
  61602. majetich
  61603. george
  61604. allylsilanes
  61605. organic
  61606. synthesis
  61607. review
  61608. makela
  61609. korpela
  61610. chemical
  61611. models
  61612. enzymic
  61613. review
  61614. makhametsin
  61615. hypofluorites
  61616. their
  61617. application
  61618. review
  61619. makosza
  61620. vicarious
  61621. nucleophilic
  61622. substitution
  61623. review
  61624. makosza
  61625. mieczyslaw
  61626. vicarious
  61627. nucleophilic
  61628. substitut
  61629. review
  61630. malek
  61631. jaroslav
  61632. reductions
  61633. metal
  61634. alkoxyaluminum
  61635. review
  61636. maletina
  61637. yagupol'skii
  61638. fluorine
  61639. review
  61640. malkin
  61641. kuz'min
  61642. photochemistry
  61643. azine
  61644. review
  61645. mallory
  61646. mallory
  61647. photocyclization
  61648. stilben
  61649. review
  61650. mandel'shtam
  61651. carbonylcarbenes
  61652. specific
  61653. review
  61654. mander
  61655. strategies
  61656. construction
  61657. review
  61658. mander
  61659. lewis
  61660. synthetic
  61661. studies
  61662. gibberellins
  61663. review
  61664. manhas
  61665. maghar
  61666. wagle
  61667. dilip
  61668. chiang
  61669. juiian
  61670. review
  61671. taylor
  61672. organometallic
  61673. review
  61674. mansuy
  61675. biomimetic
  61676. catalysts
  61677. selective
  61678. oxidati
  61679. review
  61680. manuilov
  61681. barkhash
  61682. recent
  61683. trends
  61684. review
  61685. mar'in
  61686. vyshinskaya
  61687. razuvaev
  61688. thermal
  61689. review
  61690. maramatsu
  61691. takashi
  61692. ikegami
  61693. yusaku
  61694. hanaya
  61695. kaoru
  61696. review
  61697. marchand
  61698. stereochemical
  61699. applications
  61700. review
  61701. marchand
  61702. synthesis
  61703. chemistry
  61704. homocuba
  61705. review
  61706. marchand
  61707. chemistry
  61708. pentacyclo
  61709. 5.4.0.0
  61710. review
  61711. maretina
  61712. tsil'ko
  61713. zaichenko
  61714. synthes
  61715. review
  61716. margaretha
  61717. preparative
  61718. organic
  61719. photochemistry
  61720. review
  61721. mariano
  61722. electron
  61723. transfer
  61724. mechanisms
  61725. photoch
  61726. review
  61727. mariano
  61728. photochemistry
  61729. iminium
  61730. salts
  61731. review
  61732. marina
  61733. monakov
  61734. rafikov
  61735. ponomarenko
  61736. review
  61737. markaryan
  61738. samodurova
  61739. advances
  61740. chemis
  61741. review
  61742. markgraf
  61743. infrared
  61744. carbonyl
  61745. frequencies
  61746. thiol
  61747. review
  61748. marko
  61749. marko
  61750. monostory
  61751. complexes
  61752. sulphur
  61753. review
  61754. markov
  61755. light
  61756. induced
  61757. tautomerism
  61758. dicarbonyl
  61759. review
  61760. markovskii
  61761. pashinnik
  61762. fluorination
  61763. organi
  61764. review
  61765. markovskii
  61766. romanenko
  61767. phosphaalkynes
  61768. review
  61769. markovsky
  61770. leonid
  61771. pashinnik
  61772. valerij
  61773. fluorosulfuranes
  61774. review
  61775. marks
  61776. tobin
  61777. gagne
  61778. michel
  61779. nolan
  61780. steven
  61781. schock
  61782. review
  61783. marshall
  61784. carbon
  61785. carbon
  61786. carbon
  61787. proton
  61788. review
  61789. marshall
  61790. james
  61791. additions
  61792. organocopper
  61793. review
  61794. martin
  61795. mayer
  61796. proximity
  61797. effects
  61798. organic
  61799. review
  61800. martin
  61801. nazario
  61802. seoane
  61803. carlos
  61804. hanack
  61805. michael
  61806. recent
  61807. review
  61808. martinek
  61809. semenov
  61810. enzyme
  61811. catalysis
  61812. organic
  61813. review
  61814. martynov
  61815. yurtanov
  61816. nitrocarboxylic
  61817. review
  61818. maruoka
  61819. keiji
  61820. yamamoto
  61821. hisashi
  61822. organoaluminums
  61823. review
  61824. maruyama
  61825. kazuhiro
  61826. katagiri
  61827. toshimasa
  61828. mechanism
  61829. review
  61830. maryanoff
  61831. bruce
  61832. reitz
  61833. allen
  61834. wittig
  61835. olefinat
  61836. review
  61837. maryanoff
  61838. maryanoff
  61839. synthesis
  61840. utilizati
  61841. review
  61842. masamune
  61843. advances
  61844. stereochemical
  61845. contro
  61846. review
  61847. masamune
  61848. satoru
  61849. asymmetric
  61850. synthesis
  61851. applic
  61852. review
  61853. mason
  61854. stephen
  61855. biomolecularhomochir
  61856. 198817
  61857. review
  61858. mason
  61859. stephen
  61860. development
  61861. concepts
  61862. review
  61863. massey
  61864. humphries
  61865. direct
  61866. synthesis
  61867. review
  61868. massiot
  61869. delaude
  61870. african
  61871. strychnos
  61872. alkaloids
  61873. review
  61874. mastryukova
  61875. kabachnik
  61876. phosphorus
  61877. carbon
  61878. review
  61879. mastryukova
  61880. aminophosphinocarbox
  61881. acids
  61882. review
  61883. mathey
  61884. francois
  61885. chemistry
  61886. membered
  61887. carbonphosp
  61888. review
  61889. matnishyan
  61890. kobryanskii
  61891. characteristic
  61892. featu
  61893. review
  61894. matsubayashi
  61895. structures
  61896. properties
  61897. review
  61898. matsuda
  61899. fuyuhiko
  61900. kawasaki
  61901. motoji
  61902. terashima
  61903. shiro
  61904. review
  61905. matsui
  61906. hasubanan
  61907. alkaloids
  61908. alkaloids
  61909. chemistr
  61910. review
  61911. mattay
  61912. photoinduced
  61913. electron
  61914. transfer
  61915. organic
  61916. review
  61917. mattes
  61918. farid
  61919. photochemical
  61920. cycloadditions
  61921. review
  61922. matteson
  61923. donald
  61924. recent
  61925. advances
  61926. asymmetric
  61927. review
  61928. matteson
  61929. donald
  61930. alpha
  61931. boronic
  61932. esters
  61933. interme
  61934. review
  61935. matteson
  61936. donald
  61937. boronic
  61938. esters
  61939. stereodirected
  61940. review
  61941. mavrov
  61942. advances
  61943. chemistry
  61944. halogenoa
  61945. review
  61946. maxtell
  61947. arthur
  61948. organization
  61949. molecular
  61950. review
  61951. herbert
  61952. carbon
  61953. carbon
  61954. formation
  61955. additi
  61956. review
  61957. mcclelland
  61958. santry
  61959. reactivity
  61960. tetrahedral
  61961. review
  61962. mccloskey
  61963. james
  61964. structural
  61965. characterization
  61966. review
  61967. mcdaniel
  61968. christopher
  61969. bradshaw
  61970. jerald
  61971. izatt
  61972. review
  61973. mcdermott
  61974. spillane
  61975. synthesis
  61976. reactions
  61977. review
  61978. mcdonald
  61979. richard
  61980. generation
  61981. thermochemistry
  61982. review
  61983. mcgill
  61984. charles
  61985. rappa
  61986. angela
  61987. advances
  61988. chich
  61989. review
  61990. mcgrath
  61991. riffle
  61992. polymerization
  61993. cyclosilox
  61994. review
  61995. mcmurry
  61996. titanium
  61997. induced
  61998. dicarbonyl
  61999. coupling
  62000. review
  62001. mcmurry
  62002. carbonyl
  62003. coupling
  62004. reactions
  62005. using
  62006. review
  62007. mcmurry
  62008. thomas
  62009. raymond
  62010. kenneth
  62011. smith
  62012. review
  62013. matteson
  62014. donald
  62015. alpha
  62016. boronic
  62017. esters
  62018. interme@
  62019. review
  62020. mechoulam
  62021. alkaloids
  62022. cannabis
  62023. sativa
  62024. alka@
  62025. review
  62026. mezey
  62027. developments
  62028. molecular
  62029. chira@
  62030. review
  62031. milstem
  62032. alkyl
  62033. acylrhodium
  62034. iridium@
  62035. review
  62036. mitchell
  62037. reginald
  62038. dihydropyrenes
  62039. bridged
  62040. annul@
  62041. review
  62042. kenji
  62043. synthesis
  62044. indispensable
  62045. review
  62046. mukaiyama
  62047. directed
  62048. aldol
  62049. reaction
  62050. review
  62051. murray
  62052. robert
  62053. chemistry
  62054. dioxiranes
  62055. dioxiran@
  62056. review
  62057. azirines
  62058. chemistry
  62059. heterocyclic
  62060. compounds@
  62061. review
  62062. negishi
  62063. metal
  62064. organic
  62065. approach
  62066. stereosel@
  62067. review
  62068. ninomiya
  62069. naito
  62070. photochemical
  62071. synthesis
  62072. acad@
  62073. review
  62074. noyori
  62075. uchiyama
  62076. wakabayashi
  62077. hayakawa
  62078. review
  62079. shigeru
  62080. ligand
  62081. coupling
  62082. reactions
  62083. within
  62084. hyperv@
  62085. review
  62086. ohmoto
  62087. koike
  62088. canthin
  62089. alkaloids
  62090. alkalo@
  62091. review
  62092. mechoulam
  62093. alkaloids
  62094. cannabis
  62095. sativa
  62096. review
  62097. mehrotra
  62098. chemistry
  62099. metal
  62100. diketonates
  62101. review
  62102. meinel
  62103. chemistry
  62104. applicable
  62105. review
  62106. melent'eva
  62107. structure
  62108. reactivity
  62109. review
  62110. meller
  62111. anton
  62112. borylation
  62113. aromatic
  62114. compounds
  62115. review
  62116. memory
  62117. wilson
  62118. aromatic
  62119. compounds
  62120. review
  62121. menger
  62122. directionality
  62123. organic
  62124. reactions
  62125. review
  62126. mautner
  62127. structurally
  62128. complex
  62129. organic
  62130. review
  62131. merkuhhev
  62132. advances
  62133. synthesis
  62134. aromatic
  62135. review
  62136. metalation
  62137. reactions
  62138. isocyanides
  62139. murakami
  62140. review
  62141. metgner
  62142. patrick
  62143. thiocarbonyl
  62144. compounds
  62145. organic
  62146. review
  62147. tarnowski
  62148. cyclizations
  62149. under
  62150. vilsmeie
  62151. review
  62152. methods
  62153. synthesis
  62154. allylsilanes
  62155. sarkar
  62156. review
  62157. meyer
  62158. bernd
  62159. conformational
  62160. aspects
  62161. oligosacchari
  62162. review
  62163. meyerstein
  62164. factors
  62165. affecting
  62166. equilibrium
  62167. review
  62168. mezey
  62169. developments
  62170. molecular
  62171. chira
  62172. review
  62173. mezhetritskii
  62174. valerii
  62175. tkachenko
  62176. synthesis
  62177. review
  62178. michalska
  62179. maria
  62180. michalski
  62181. glycosyl
  62182. review
  62183. michalski
  62184. lopusinski
  62185. andrzej
  62186. organophosphorus
  62187. review
  62188. michl
  62189. magnetic
  62190. circular
  62191. dichroism
  62192. aromatic
  62193. review
  62194. michl
  62195. joseph
  62196. bonacic
  62197. koutecky
  62198. vlasta
  62199. electronic
  62200. review
  62201. midland
  62202. reductions
  62203. chiral
  62204. boron
  62205. reagents
  62206. review
  62207. midland
  62208. asymmetric
  62209. reductions
  62210. organobor
  62211. review
  62212. mikolajczyk
  62213. drabowica
  62214. chiral
  62215. solvating
  62216. review
  62217. mikolajczyk
  62218. drabowicz
  62219. chiral
  62220. organosulfur
  62221. compo
  62222. review
  62223. mikolajczyk
  62224. marian
  62225. phosphonate
  62226. carbanions
  62227. review
  62228. milaeva
  62229. rubezhov
  62230. prokof'ev
  62231. okhlobystin
  62232. review
  62233. miller
  62234. organic
  62235. plasma
  62236. chemistry
  62237. 198316
  62238. review
  62239. miller
  62240. marvin
  62241. synthesis
  62242. therapeutic
  62243. potential
  62244. review
  62245. mills
  62246. maryanoff
  62247. cosgrove
  62248. scott
  62249. mccoms
  62250. review
  62251. milstem
  62252. alkyl
  62253. acylrhodium
  62254. iridium
  62255. review
  62256. mimoun
  62257. oxygen
  62258. transfer
  62259. inorganic
  62260. organic
  62261. review
  62262. minisci
  62263. citterio
  62264. giordano
  62265. electron
  62266. transfer
  62267. review
  62268. minisci
  62269. francesco
  62270. vismara
  62271. elena
  62272. fontana
  62273. francesca
  62274. review
  62275. minkin
  62276. simkin
  62277. glukhovtsev
  62278. quantum
  62279. review
  62280. minkin
  62281. minyaev
  62282. polyhedral
  62283. organic
  62284. molecules
  62285. review
  62286. mintz
  62287. preparation
  62288. reactivity
  62289. zircon
  62290. review
  62291. mirbach
  62292. mirbach
  62293. pressure
  62294. photoc
  62295. review
  62296. mironov
  62297. federovich
  62298. akhrem
  62299. synthetic
  62300. review
  62301. mironov
  62302. fedorovich
  62303. akhrem
  62304. shift
  62305. review
  62306. mirskova
  62307. drozdova
  62308. levkovskaya
  62309. voronkov
  62310. review
  62311. mirskova
  62312. seredkina
  62313. voronkov
  62314. organothio
  62315. review
  62316. mislow
  62317. molecular
  62318. machinery
  62319. organic
  62320. chemistry
  62321. review
  62322. misumi
  62323. multilayered
  62324. cyclophanes
  62325. cyclophanes
  62326. review
  62327. mitchell
  62328. nuclear
  62329. magnetic
  62330. resonance
  62331. properties
  62332. review
  62333. mitchell
  62334. reginald
  62335. dihydropyrenes
  62336. bridged
  62337. annul
  62338. review
  62339. miura
  62340. masahiro
  62341. nomura
  62342. masakatsu
  62343. desulfonylative
  62344. review
  62345. miura
  62346. syntheses
  62347. chemical
  62348. behaviors
  62349. review
  62350. miyakoshi
  62351. tetsuo
  62352. preparation
  62353. reactions
  62354. review
  62355. miyashi
  62356. tsutomu
  62357. ikeda
  62358. hiroshi
  62359. komno
  62360. akmori
  62361. okitsu
  62362. review
  62363. mizuno
  62364. nomura
  62365. azanucleosides
  62366. deazanu
  62367. review
  62368. mndzhoyan
  62369. topuzyan
  62370. methods
  62371. synthesis
  62372. review
  62373. moiseev
  62374. carbene
  62375. complexes
  62376. catalysis
  62377. review
  62378. molander
  62379. mautner
  62380. konrad
  62381. novel
  62382. processes
  62383. review
  62384. mondon
  62385. bitter
  62386. principles
  62387. cneoraceae
  62388. review
  62389. montanari
  62390. landini
  62391. rolla
  62392. phase
  62393. transfer
  62394. cataly
  62395. review
  62396. moody
  62397. azodicarbonyl
  62398. compounds
  62399. heterocyclic
  62400. review
  62401. moore
  62402. gheorghiu
  62403. cyanoketenes
  62404. synthesis
  62405. review
  62406. moore
  62407. ayers
  62408. azetidines
  62409. chemistry
  62410. heteroc
  62411. review
  62412. morgan
  62413. michael
  62414. mycotoxin
  62415. immunoassays
  62416. review
  62417. kenji
  62418. synthesis
  62419. indispensable
  62420. review
  62421. kenji
  62422. synthesis
  62423. optically
  62424. active
  62425. pheromones
  62426. review
  62427. kenji
  62428. watanabe
  62429. hidenori
  62430. recent
  62431. results
  62432. review
  62433. moriarty
  62434. robert
  62435. radhe
  62436. carbon
  62437. carbon
  62438. review
  62439. morris
  62440. carbonyl
  62441. group
  62442. transpositiong
  62443. 198211
  62444. review
  62445. morris
  62446. recent
  62447. advances
  62448. chemistry
  62449. review
  62450. morrison
  62451. harry
  62452. bioorganic
  62453. photochemistry
  62454. review
  62455. morrison
  62456. summary
  62457. obtain
  62458. optically
  62459. review
  62460. morrison
  62461. chemistry
  62462. polyhedral
  62463. boron
  62464. review
  62465. morton
  62466. phase
  62467. analogues
  62468. solvolysis
  62469. reacti
  62470. review
  62471. jones
  62472. carbenes
  62473. reactive
  62474. intermed
  62475. review
  62476. robert
  62477. carbenic
  62478. reactivity
  62479. revisited
  62480. review
  62481. muccino
  62482. organic
  62483. synthesis
  62484. carbon
  62485. wiley
  62486. review
  62487. muetterties
  62488. bleeke
  62489. wucherer
  62490. albright
  62491. review
  62492. muetterties
  62493. hydrocarbon
  62494. reactions
  62495. metal
  62496. review
  62497. mukaiyama
  62498. directed
  62499. aldol
  62500. reaction
  62501. review
  62502. mukayiama
  62503. teruaki
  62504. challenges
  62505. synthetic
  62506. organic
  62507. review
  62508. mukerjee
  62509. ashare
  62510. isothiocyanates
  62511. review
  62512. mullen
  62513. reduction
  62514. oxidation
  62515. annulenes
  62516. review
  62517. muller
  62518. organofluorosilicate
  62519. chemistry
  62520. silico
  62521. review
  62522. mulzer
  62523. johann
  62524. organic
  62525. synthesis
  62526. highlights
  62527. review
  62528. mundy
  62529. ellerd
  62530. reactions
  62531. reagents
  62532. review
  62533. murahashi
  62534. naota
  62535. takeshi
  62536. ruthenium
  62537. catalyz
  62538. review
  62539. murakami
  62540. tanaka
  62541. occurrence
  62542. structure
  62543. taxono
  62544. review
  62545. murakami
  62546. functionalized
  62547. cyclophanes
  62548. catalysts
  62549. review
  62550. murakami
  62551. yukito
  62552. kikucchi
  62553. teruhisa
  62554. review
  62555. murata
  62556. nakasuki
  62557. recent
  62558. advances
  62559. thiepin
  62560. review
  62561. murphy
  62562. brennan
  62563. wittig
  62564. olefination
  62565. reactio
  62566. review
  62567. murphy
  62568. sattanasin
  62569. anionic
  62570. cyclization
  62571. review
  62572. murray
  62573. mendez
  62574. brown
  62575. natural
  62576. review
  62577. murray
  62578. robert
  62579. chemistry
  62580. dioxiranes
  62581. dioxiran
  62582. review
  62583. musker
  62584. kenneth
  62585. joyce
  62586. takahashi
  62587. heterocyclic
  62588. review
  62589. mutter
  62590. manfred
  62591. vuilleumier
  62592. stephane
  62593. chemical
  62594. review
  62595. myles
  62596. david
  62597. danishefsky
  62598. samuel
  62599. synthesis
  62600. review
  62601. celebi
  62602. fabad
  62603. cyclodextrins
  62604. review
  62605. furakawa
  62606. synth
  62607. reactio
  62608. review
  62609. kochetkov
  62610. tetrahedron
  62611. tetrahedron
  62612. review
  62613. bauld
  62614. cation
  62615. review
  62616. mizuno
  62617. misono
  62618. synth
  62619. review
  62620. isaacs
  62621. goerge
  62622. chemic
  62623. review
  62624. zefirov
  62625. approach
  62626. review
  62627. naddaka
  62628. sadekov
  62629. maksimenko
  62630. minkin
  62631. review
  62632. nagao
  62633. fujita
  62634. practical
  62635. synthetic
  62636. method
  62637. review
  62638. nagata
  62639. narisada
  62640. yoshida
  62641. partial
  62642. synthesis
  62643. review
  62644. nagata
  62645. wataru
  62646. contributions
  62647. chemistry
  62648. review
  62649. azirines
  62650. chemistry
  62651. heterocyclic
  62652. compounds
  62653. review
  62654. nakagaki
  62655. ryoichi
  62656. sakuragi
  62657. hirochika
  62658. mutai
  62659. kiyoshi
  62660. review
  62661. nakasuji
  62662. kazuhiro
  62663. multi
  62664. stage
  62665. redox
  62666. systems
  62667. review
  62668. nakayama
  62669. akimoto
  62670. keiichi
  62671. hoshino
  62672. masamatsu
  62673. review
  62674. nakayama
  62675. konishi
  62676. hoshino
  62677. masamatsu
  62678. prepar
  62679. review
  62680. nakazaki
  62681. synthesis
  62682. stereochemistry
  62683. review
  62684. narang
  62685. synthesis
  62686. tetrahedron
  62687. review
  62688. narasaka
  62689. koichi
  62690. chiral
  62691. lewis
  62692. acids
  62693. catalytic
  62694. review
  62695. narisimban
  62696. syntheses
  62697. heterocyclic
  62698. review
  62699. natale
  62700. lanthanides
  62701. organic
  62702. synthesis
  62703. review
  62704. naylor
  62705. hanke
  62706. mames
  62707. crews
  62708. chemical
  62709. review
  62710. nefedov
  62711. chemistry
  62712. carbenes
  62713. small
  62714. sized
  62715. review
  62716. nefedov
  62717. generation
  62718. temperature
  62719. stabilizatio
  62720. review
  62721. negishi
  62722. idacavage
  62723. formation
  62724. carbon
  62725. carbo
  62726. review
  62727. negishi
  62728. palladium
  62729. nickel
  62730. catalyzed
  62731. cross
  62732. review
  62733. negishi
  62734. metal
  62735. organic
  62736. approach
  62737. stereosel
  62738. review
  62739. negishi
  62740. eiichi
  62741. cyclization
  62742. coupling
  62743. rearrangeme
  62744. review
  62745. fuller
  62746. isopentenoids
  62747. plants
  62748. review
  62749. neumann
  62750. wilhelm
  62751. hillgaertner
  62752. horst
  62753. baines
  62754. review
  62755. methods
  62756. synthesis
  62757. troponoid
  62758. compound
  62759. review
  62760. newkome
  62761. paudler
  62762. contemporary
  62763. heterocyclic
  62764. review
  62765. newton
  62766. ramsden
  62767. ionic
  62768. heterocycles
  62769. review
  62770. newton
  62771. recent
  62772. syntheses
  62773. prostaglandins
  62774. review
  62775. newton
  62776. roberts
  62777. taylor
  62778. strategies
  62779. review
  62780. nibbering
  62781. phase
  62782. ion/molecule
  62783. reactions
  62784. review
  62785. nibbering
  62786. phase
  62787. reactions
  62788. organic
  62789. review
  62790. nicholson
  62791. jeremy
  62792. wilson
  62793. resolution
  62794. review
  62795. nicolaou
  62796. petaisis
  62797. selenium
  62798. natural
  62799. produ
  62800. review
  62801. nifant'ev
  62802. zavalishina
  62803. advances
  62804. chemi
  62805. review
  62806. nikitina
  62807. trifluorostyrene
  62808. polymers
  62809. review
  62810. ninomiya
  62811. naito
  62812. photochemical
  62813. synthesis
  62814. review
  62815. ninomiya
  62816. naito
  62817. application
  62818. enamide
  62819. cycli
  62820. review
  62821. ninomiya
  62822. ichiya
  62823. kiguchi
  62824. toshiko
  62825. ergot
  62826. alkaloids
  62827. review
  62828. nishio
  62829. motohiro
  62830. hirota
  62831. minoru
  62832. interaction
  62833. review
  62834. shimohigashi
  62835. izumiya
  62836. dehydropeptides
  62837. review
  62838. noeth
  62839. heinrich
  62840. geisberger
  62841. gilbert
  62842. linti
  62843. gerald
  62844. review
  62845. nomura
  62846. phenolic
  62847. compounds
  62848. mulberry
  62849. review
  62850. norin
  62851. torbjoern
  62852. synthetic
  62853. chemical
  62854. studies
  62855. review
  62856. normant
  62857. organobismetallic
  62858. reagents
  62859. preparation
  62860. review
  62861. novotny
  62862. milos
  62863. recent
  62864. developments
  62865. analytical
  62866. review
  62867. noyori
  62868. chemical
  62869. multiplication
  62870. chirality
  62871. scien
  62872. review
  62873. noyori
  62874. hayakawa
  62875. reductive
  62876. dehalogenation
  62877. review
  62878. noyori
  62879. suzuki
  62880. organometallic
  62881. prostagl
  62882. review
  62883. noyori
  62884. suzuki
  62885. prostaglandin
  62886. synthesis
  62887. three
  62888. review
  62889. noyori
  62890. uchiyama
  62891. wakabayashi
  62892. hayakawa
  62893. review
  62894. noyori
  62895. uchiyama
  62896. wakabayashi
  62897. hayakawa
  62898. review
  62899. noyori
  62900. ryoji
  62901. chiral
  62902. metal
  62903. complexes
  62904. discriminati
  62905. review
  62906. noyori
  62907. ryoji
  62908. kitamura
  62909. maaato
  62910. enantioselective
  62911. addit
  62912. review
  62913. noyori
  62914. ryoji
  62915. prostaglandins
  62916. simple
  62917. review
  62918. noyori
  62919. ryoji
  62920. takaya
  62921. hidemasa
  62922. binap
  62923. efficient
  62924. review
  62925. nozoe
  62926. tetsuo
  62927. cyclohepta
  62928. benzoxazine
  62929. review
  62930. nudelman
  62931. chemistry
  62932. optically
  62933. active
  62934. sulfur
  62935. review
  62936. nudelman
  62937. norma
  62938. dimer
  62939. mechanism
  62940. aromatic
  62941. review
  62942. nyiredy
  62943. szabolics
  62944. optimization
  62945. mobile
  62946. phase
  62947. review
  62948. attanasi
  62949. caglioti
  62950. proced
  62951. review
  62952. furukawa
  62953. sulfilimines
  62954. related
  62955. derivativ
  62956. review
  62957. shinhama
  62958. organic
  62959. thionitrites
  62960. related
  62961. review
  62962. shigeru
  62963. chemical
  62964. behavior
  62965. elemental
  62966. sulfur
  62967. review
  62968. shigeru
  62969. furukawa
  62970. naomichi
  62971. heteroaromatic
  62972. sulfox
  62973. review
  62974. shigeru
  62975. ligand
  62976. coupling
  62977. reactions
  62978. hyperval
  62979. review
  62980. shigeru
  62981. ligand
  62982. coupling
  62983. reactions
  62984. within
  62985. hyperv
  62986. review
  62987. shigeru
  62988. uchida
  62989. yuzuru
  62990. validity
  62991. conce
  62992. review
  62993. david
  62994. heathcock
  62995. clayton
  62996. stereochemistry
  62997. review
  62998. david
  62999. heathcock
  63000. clayton
  63001. acyclic
  63002. stereocont
  63003. review
  63004. oberhauser
  63005. faber
  63006. griengl
  63007. substrate
  63008. model
  63009. review
  63010. occolowitz
  63011. hamill
  63012. spectrometry
  63013. review
  63014. ochiai
  63015. masihito
  63016. hypervalentalkyliodi
  63017. chemistry
  63018. review
  63019. odashima
  63020. cyclophanes
  63021. guest
  63022. chemist
  63023. review
  63024. odinokov
  63025. tolstikov
  63026. ozonolysis
  63027. modern
  63028. review
  63029. annulation
  63030. review
  63031. reagents
  63032. review
  63033. dendritic
  63034. macromolecules
  63035. review
  63036. curtin
  63037. hammett
  63038. principle
  63039. analysis
  63040. review
  63041. peterson
  63042. reaction
  63043. review
  63044. sakurai
  63045. reaction
  63046. using
  63047. allylic
  63048. silanes
  63049. review
  63050. ogura
  63051. kyozo
  63052. artificially
  63053. elicited
  63054. capabilities
  63055. review
  63056. ohmoto
  63057. koike
  63058. canthin
  63059. alkaloids
  63060. alkalo
  63061. review
  63062. masaji
  63063. natural
  63064. bleomycins
  63065. designed
  63066. review
  63067. masaji
  63068. otsuka
  63069. masami
  63070. chiral
  63071. synthons
  63072. ester
  63073. review
  63074. ohshiro
  63075. hirao
  63076. heterocyclic
  63077. synthesis
  63078. metal
  63079. review
  63080. oishi
  63081. nakata
  63082. introduction
  63083. chiral
  63084. centers
  63085. review
  63086. ojima
  63087. nuria
  63088. bastos
  63089. ceclia
  63090. recent
  63091. advances
  63092. review
  63093. ojima
  63094. carbonylations
  63095. means
  63096. transitio
  63097. review
  63098. okamoto
  63099. kaoru
  63100. toshio
  63101. glycosidation
  63102. sialic
  63103. review
  63104. okamoto
  63105. kunio
  63106. generation
  63107. structures
  63108. review
  63109. okamura
  63110. pericyclic
  63111. reactions
  63112. vinylallenes
  63113. review
  63114. reactivity
  63115. conformational
  63116. isomers
  63117. 198417
  63118. review
  63119. recent
  63120. advances
  63121. atropisomerism
  63122. 198314
  63123. review
  63124. michinori
  63125. disubstituted
  63126. triptycenes
  63127. review
  63128. okuda
  63129. takuo
  63130. yoshida
  63131. takashi
  63132. hatano
  63133. tsutomu
  63134. oligomer
  63135. review
  63136. okuyama
  63137. tadashi
  63138. stability
  63139. reactivity
  63140. dithio
  63141. review
  63142. malhotra
  63143. narang
  63144. nitration
  63145. methods
  63146. review
  63147. narang
  63148. iodotrimethylsilane
  63149. versatile
  63150. review
  63151. prakash
  63152. saunders
  63153. conclusion
  63154. review
  63155. george
  63156. hydrocarbons
  63157. wiley
  63158. review
  63159. george
  63160. prakach
  63161. surya
  63162. krishnamurthy
  63163. rames
  63164. review
  63165. george
  63166. kenneth
  63167. williams
  63168. robert
  63169. electr
  63170. review
  63171. olofson
  63172. useful
  63173. reactions
  63174. novel
  63175. halofor
  63176. review
  63177. olsen
  63178. quinoxaline
  63179. depsipeptide
  63180. antibiotics
  63181. review
  63182. organotin
  63183. chemistry
  63184. journal
  63185. organometalli
  63186. review
  63187. takahashi
  63188. protopine
  63189. alkaloids
  63190. alkaloid
  63191. review
  63192. trichothecanes
  63193. review
  63194. 1982191685
  63195. heterocy
  63196. review
  63197. oppolzer
  63198. asymmetric
  63199. diels
  63200. alder
  63201. reactions
  63202. review
  63203. oppolzer
  63204. intramolecular
  63205. photoaddition
  63206. cyclobu
  63207. review
  63208. oppolzer
  63209. intramolecular
  63210. stoichiometric
  63211. review
  63212. oppolzer
  63213. regio
  63214. stereocontrolled
  63215. catalytic
  63216. review
  63217. malhotra
  63218. narang
  63219. nitration
  63220. methods
  63221. review
  63222. oppolzer
  63223. wolfgang
  63224. metal
  63225. directed
  63226. stereoselective
  63227. review
  63228. padwa
  63229. dipolar
  63230. cycloaddition
  63231. chemistry
  63232. wiley@
  63233. review
  63234. paquette
  63235. dodecahedranes
  63236. allied
  63237. spherical
  63238. review
  63239. patai
  63240. rappoport
  63241. chemistry
  63242. organ
  63243. review
  63244. pedersen
  63245. dithiole
  63246. thiones
  63247. dithiol
  63248. review
  63249. peter
  63250. martin
  63251. chemical
  63252. modification
  63253. biopolymers@
  63254. review
  63255. pickart
  63256. peptide
  63257. protein
  63258. complexes
  63259. transiti@
  63260. review
  63261. michael
  63262. mueller
  63263. achim
  63264. polyoxometalate
  63265. chemis@
  63266. review
  63267. prelog
  63268. helmchen
  63269. basic
  63270. principles
  63271. review
  63272. quinou
  63273. herve
  63274. guilloton
  63275. odette
  63276. thiazines
  63277. review
  63278. radchenko
  63279. petrov
  63280. acetylenic
  63281. ethers
  63282. thei@
  63283. review
  63284. ramaiah
  63285. cyclopentannelltion
  63286. reactions
  63287. organic
  63288. review
  63289. rebek
  63290. julius
  63291. heterocycles
  63292. molecular
  63293. recognit@
  63294. review
  63295. oppolzer
  63296. wolfgang
  63297. metal
  63298. directed
  63299. stereoselective
  63300. review
  63301. osawa
  63302. musso
  63303. applications
  63304. molecular
  63305. mechanics
  63306. review
  63307. osawa
  63308. musso
  63309. molecular
  63310. mechanics
  63311. calculations
  63312. review
  63313. osawa
  63314. hitoshi
  63315. oishi
  63316. takeshi
  63317. ohtsuka
  63318. yasuo
  63319. review
  63320. oshima
  63321. koichioro
  63322. transition
  63323. metal
  63324. catalyzed
  63325. silylme
  63326. review
  63327. oshry
  63328. rosenfeld
  63329. synthesis
  63330. review
  63331. overman
  63332. mercury
  63333. palladium
  63334. catalyzed
  63335. review
  63336. chaloner
  63337. organomet
  63338. nickel
  63339. review
  63340. chaloner
  63341. organomet
  63342. nickel
  63343. review
  63344. shapley
  63345. organomet
  63346. annual
  63347. review
  63348. sutton
  63349. buckingham
  63350. review
  63351. baraldi
  63352. synthesis
  63353. synthesis
  63354. review
  63355. kovacic
  63356. jones
  63357. dehydr
  63358. review
  63359. paddon
  63360. aspects
  63361. orbital
  63362. interactions
  63363. review
  63364. padwa
  63365. carlsen
  63366. nitrile
  63367. ylides
  63368. nitrenes
  63369. review
  63370. padwa
  63371. dipolar
  63372. cycloaddition
  63373. chemistry
  63374. wiley
  63375. review
  63376. padwa
  63377. albert
  63378. generation
  63379. utilization
  63380. carbonyl
  63381. review
  63382. padwa
  63383. albert
  63384. schoffstall
  63385. allen
  63386. intramolecular
  63387. review
  63388. paetzold
  63389. perspectives
  63390. boron
  63391. nitrogen
  63392. chemi
  63393. review
  63394. mechanisms
  63395. reactions
  63396. lactam
  63397. review
  63398. philip
  63399. bulmam
  63400. sukhbmder
  63401. klair
  63402. rosenthal
  63403. review
  63404. philip
  63405. bulman
  63406. monique
  63407. prodger
  63408. review
  63409. pagni
  63410. multiply
  63411. charged
  63412. carbocations
  63413. related
  63414. review
  63415. painter
  63416. pressman
  63417. dynamic
  63418. aspects
  63419. ionopho
  63420. review
  63421. painter
  63422. george
  63423. shockor
  63424. andrews
  63425. webster
  63426. review
  63427. pankratov
  63428. frenkel
  63429. fainleib
  63430. oxazolidi
  63431. review
  63432. pannell
  63433. organosilicon
  63434. transition
  63435. metal
  63436. interact
  63437. review
  63438. paquette
  63439. asymmetric
  63440. cycloaddition
  63441. reactions
  63442. review
  63443. paquette
  63444. recent
  63445. synthetic
  63446. developments
  63447. polyq
  63448. review
  63449. paquette
  63450. synthetic
  63451. routes
  63452. cyclopenenoid
  63453. review
  63454. paquette
  63455. dodecahedranes
  63456. allied
  63457. spherical
  63458. review
  63459. paquette
  63460. stereocontrolled
  63461. construction
  63462. review
  63463. parham
  63464. bradsher
  63465. aromatic
  63466. organolithium
  63467. review
  63468. parker
  63469. reaction
  63470. pathways
  63471. cation
  63472. radicals
  63473. review
  63474. parker
  63475. study
  63476. reactive
  63477. intermediates
  63478. review
  63479. parry
  63480. biosynthesis
  63481. sulfur
  63482. containing
  63483. review
  63484. parshall
  63485. george
  63486. nugent
  63487. william
  63488. making
  63489. pharmaceu
  63490. review
  63491. pasto
  63492. recent
  63493. developments
  63494. allene
  63495. chemistry
  63496. review
  63497. pasynskii
  63498. eremenko
  63499. heterometallic
  63500. sulfide
  63501. review
  63502. patai
  63503. chemistry
  63504. double
  63505. bonded
  63506. functi
  63507. review
  63508. patai
  63509. chemistry
  63510. sulphenic
  63511. acids
  63512. review
  63513. patai
  63514. chemistry
  63515. sulphinic
  63516. acids
  63517. review
  63518. patai
  63519. patai's
  63520. guide
  63521. chemistry
  63522. fumcti
  63523. review
  63524. patai
  63525. rappoport
  63526. chemistry
  63527. enone
  63528. review
  63529. patai
  63530. rappoport
  63531. chemistry
  63532. organ
  63533. review
  63534. patai
  63535. rappoport
  63536. chemistry
  63537. organ
  63538. review
  63539. patai
  63540. rappoport
  63541. chemistry
  63542. review
  63543. paton
  63544. michael
  63545. chemistry
  63546. nitrile
  63547. sulfides
  63548. review
  63549. paton
  63550. michael
  63551. chemistry
  63552. nitrile
  63553. sulfides
  63554. review
  63555. pattenden
  63556. gerald
  63557. cobalt
  63558. mediated
  63559. radical
  63560. reactions
  63561. review
  63562. paudler
  63563. heterocyclophanes
  63564. cyclophanes
  63565. keehn
  63566. review
  63567. paudler
  63568. jovanovic
  63569. backdonation
  63570. irrelati
  63571. review
  63572. paudler
  63573. sheets
  63574. recent
  63575. developments
  63576. napht
  63577. review
  63578. edward
  63579. reaction
  63580. systems
  63581. pharmaceutica
  63582. review
  63583. paulsen
  63584. advances
  63585. selective
  63586. chemical
  63587. syntheses
  63588. review
  63589. paulsen
  63590. synthesis
  63591. conformations
  63592. review
  63593. pavlenko
  63594. vapor
  63595. phase
  63596. heterogeneous
  63597. catalyti
  63598. review
  63599. pearce
  63600. medicinal
  63601. chemistry
  63602. bisindole
  63603. alkaloi
  63604. review
  63605. pearson
  63606. anthony
  63607. recent
  63608. developments
  63609. synthe
  63610. review
  63611. pedersen
  63612. dithiole
  63613. thiones
  63614. dithiol
  63615. review
  63616. pedersen
  63617. dithiole
  63618. thiones
  63619. dithiol
  63620. review
  63621. pelletier
  63622. alkaloids
  63623. chemical
  63624. biological
  63625. review
  63626. pelter
  63627. carbon
  63628. carbon
  63629. formation
  63630. involving
  63631. review
  63632. pelter
  63633. andrew
  63634. smith
  63635. keith
  63636. brown
  63637. herbert
  63638. borane
  63639. review
  63640. pelter
  63641. andrew
  63642. smith
  63643. keith
  63644. jones
  63645. kevin
  63646. synthesis
  63647. review
  63648. pelyvas
  63649. monneret
  63650. herczegh
  63651. synthetic
  63652. aspects
  63653. review
  63654. perkins
  63655. berti
  63656. corrado
  63657. brooks
  63658. deborah
  63659. grier
  63660. review
  63661. perlmutter
  63662. trattner
  63663. azocines
  63664. review
  63665. perlmutter
  63666. howard
  63667. diazocines
  63668. diazocines
  63669. review
  63670. perlmutter
  63671. howard
  63672. diazocines
  63673. 45185
  63674. review
  63675. perlmutter
  63676. howard
  63677. diazocines
  63678. advan
  63679. review
  63680. perrin
  63681. charles
  63682. proton
  63683. exchange
  63684. amides
  63685. surprise
  63686. review
  63687. perron
  63688. francoise
  63689. albizati
  63690. chemistry
  63691. spirok
  63692. review
  63693. perutz
  63694. robin
  63695. simon
  63696. mccamley
  63697. andrew
  63698. whittle
  63699. review
  63700. perutz
  63701. robin
  63702. photochemical
  63703. carbon
  63704. hydrogen
  63705. review
  63706. peter
  63707. martin
  63708. chemical
  63709. modification
  63710. biopolymers
  63711. review
  63712. peters
  63713. allen
  63714. structure
  63715. bonding
  63716. review
  63717. peterson
  63718. anderson
  63719. larson
  63720. silane
  63721. blocking
  63722. review
  63723. peterson
  63724. anderson
  63725. silane
  63726. blocking
  63727. agents
  63728. review
  63729. petragnani
  63730. yonashiro
  63731. reactions
  63732. dianions
  63733. review
  63734. petragnani
  63735. nicola
  63736. comasseto
  63737. selenium
  63738. tellu
  63739. review
  63740. petrosyan
  63741. niyazymbetov
  63742. electrochemical
  63743. review
  63744. petrov
  63745. dogadina
  63746. ionin
  63747. garibina
  63748. review
  63749. petrov
  63750. equilibrium
  63751. acidity
  63752. organic
  63753. review
  63754. petrov
  63755. chauzov
  63756. agafonov
  63757. alkoxy
  63758. compou
  63759. review
  63760. pettit
  63761. synthetic
  63762. peptides
  63763. volume
  63764. academic
  63765. review
  63766. pfander
  63767. hanspeter
  63768. synthesis
  63769. optically
  63770. active
  63771. review
  63772. pfeffer
  63773. michel
  63774. reactions
  63775. cyclopalladated
  63776. compoun
  63777. review
  63778. piancatelli
  63779. advances
  63780. cyclopentenone
  63781. synthesis
  63782. review
  63783. piancatelli
  63784. scettri
  63785. d'auria
  63786. pyridinium
  63787. chloro
  63788. review
  63789. pickart
  63790. peptide
  63791. protein
  63792. complexes
  63793. transiti
  63794. review
  63795. piers
  63796. edward
  63797. bifunctional
  63798. reagents
  63799. review
  63800. pillai
  63801. perspectives
  63802. polymer
  63803. supported
  63804. review
  63805. pindur
  63806. erfanian
  63807. abdoust
  63808. houshang
  63809. indolo
  63810. review
  63811. pinnick
  63812. potassium
  63813. hydride
  63814. organic
  63815. synthesis
  63816. review
  63817. pinnick
  63818. harold
  63819. reaction
  63820. review
  63821. pirkle
  63822. separation
  63823. enantiomers
  63824. review
  63825. pirkle
  63826. william
  63827. pochapsky
  63828. thomas
  63829. considerations
  63830. review
  63831. pizey
  63832. synthetic
  63833. reagents
  63834. mercuric
  63835. review
  63836. pizey
  63837. synthetic
  63838. reagents
  63839. volume
  63840. thallium
  63841. review
  63842. platz
  63843. matthew
  63844. kinetics
  63845. gpectroscopy
  63846. review
  63847. plesek
  63848. helmanek
  63849. stibr
  63850. early
  63851. birds
  63852. chiral
  63853. review
  63854. podraza
  63855. kenneth
  63856. regiospecific
  63857. alkylation
  63858. cyclo
  63859. review
  63860. poirier
  63861. marie
  63862. synthesis
  63863. reactions
  63864. funct
  63865. review
  63866. pollack
  63867. ralph
  63868. stereoelectronic
  63869. control
  63870. review
  63871. michael
  63872. mueller
  63873. achim
  63874. polyoxometalate
  63875. chemis
  63876. review
  63877. milan
  63878. faehnrich
  63879. tatar
  63880. vlastimil
  63881. chromatogr
  63882. review
  63883. reissert
  63884. compounds
  63885. related
  63886. acyldihyd
  63887. review
  63888. porshnev
  63889. mochalin
  63890. cherkashin
  63891. polycycli
  63892. review
  63893. porter
  63894. alexander
  63895. chemistry
  63896. thiophenium
  63897. review
  63898. porter
  63899. spurgeon
  63900. biosynthesis
  63901. isopren
  63902. review
  63903. porter
  63904. krebs
  63905. stereochemical
  63906. aspects
  63907. review
  63908. posner
  63909. addition
  63910. organometallic
  63911. reagents
  63912. review
  63913. posner
  63914. synthetic
  63915. methodology
  63916. using
  63917. organ
  63918. review
  63919. pospisil
  63920. klemchuk
  63921. peter
  63922. oxidation
  63923. inhibit
  63924. review
  63925. poulter
  63926. biosynthesis
  63927. review
  63928. power
  63929. philip
  63930. boron
  63931. phosphorus
  63932. compounds
  63933. multi
  63934. review
  63935. pozharskii
  63936. dal'nikovskaya
  63937. perimidines
  63938. review
  63939. prakash
  63940. rawdah
  63941. stable
  63942. carbodicat
  63943. review
  63944. pratt
  63945. andrew
  63946. enzymes
  63947. asymmetric
  63948. synthesis
  63949. review
  63950. prelog
  63951. helmchen
  63952. basic
  63953. principles
  63954. review
  63955. prelog
  63956. vladimir
  63957. albert
  63958. eschenmoser
  63959. review
  63960. preparation
  63961. reactions
  63962. organoruthenium
  63963. review
  63964. pretsch
  63965. clerc
  63966. seibl
  63967. simon
  63968. tables
  63969. spectra
  63970. review
  63971. proidakov
  63972. kalabin
  63973. vasilevskii
  63974. param
  63975. review
  63976. pross
  63977. radom
  63978. theoretical
  63979. approach
  63980. substitue
  63981. review
  63982. pross
  63983. shaik
  63984. qualitative
  63985. valence
  63986. approa
  63987. review
  63988. protopopova
  63989. shapiro
  63990. carbene
  63991. synthesis
  63992. review
  63993. pudovik
  63994. ovchinnikov
  63995. cherkasov
  63996. pudovik
  63997. review
  63998. pusch
  63999. watch
  64000. synthetic
  64001. membranes
  64002. preparation
  64003. review
  64004. quack
  64005. martin
  64006. structure
  64007. dynamics
  64008. chiral
  64009. molec
  64010. review
  64011. quast
  64012. photolysis
  64013. saturated
  64014. membere
  64015. review
  64016. queener
  64017. neuss
  64018. biosynthesis
  64019. lactam
  64020. review
  64021. louis
  64022. unusual
  64023. properties
  64024. phosphorus
  64025. funct
  64026. review
  64027. quinkert
  64028. stark
  64029. stereoselective
  64030. synthesis
  64031. review
  64032. quinou
  64033. herve
  64034. guilloton
  64035. odette
  64036. thiazines
  64037. review
  64038. qunia
  64039. photophysical
  64040. concepts
  64041. condensed
  64042. media
  64043. review
  64044. kerber
  64045. orqanomet
  64046. organoiron
  64047. review
  64048. grigg
  64049. prototropic
  64050. routes
  64051. review
  64052. williams
  64053. pergamon
  64054. press
  64055. organic
  64056. chemistry
  64057. review
  64058. noack
  64059. schwetlick
  64060. insertio
  64061. review
  64062. hoffman
  64063. proced
  64064. review
  64065. hoffmann
  64066. angew
  64067. review
  64068. hoffmann
  64069. hoppe
  64070. angew
  64071. review
  64072. angew
  64073. chemistr
  64074. review
  64075. raban
  64076. stereolabile
  64077. configurational
  64078. units
  64079. review
  64080. rabideau
  64081. peter
  64082. conformational
  64083. analysis
  64084. review
  64085. rabideau
  64086. peter
  64087. metal
  64088. ammonia
  64089. reduction
  64090. review
  64091. rabinovitz
  64092. mordecai
  64093. cohen
  64094. yoram
  64095. probing
  64096. nature
  64097. review
  64098. rabinovitz
  64099. mordecai
  64100. polycyclic
  64101. anions
  64102. doubly
  64103. review
  64104. radchenko
  64105. petrov
  64106. acetylenic
  64107. ethers
  64108. review
  64109. raevskii
  64110. ignat'eva
  64111. conformational
  64112. analysis
  64113. review
  64114. raevskii
  64115. structure
  64116. properties
  64117. comple
  64118. review
  64119. rahman
  64120. basha
  64121. biosynthesis
  64122. indole
  64123. alkaloids
  64124. review
  64125. rahman
  64126. studies
  64127. natural
  64128. products
  64129. chemi
  64130. review
  64131. rahman
  64132. lequesne
  64133. philip
  64134. william
  64135. natural
  64136. review
  64137. rahman
  64138. muzaffar
  64139. steroidal
  64140. alkaloids
  64141. review
  64142. rahman
  64143. mckee
  64144. shevlin
  64145. reactions
  64146. review
  64147. rajopadhye
  64148. milind
  64149. frank
  64150. chemistry
  64151. benzo
  64152. review
  64153. rakhmankulov
  64154. zlotskii
  64155. zorin
  64156. imashev
  64157. review
  64158. rakhmankulov
  64159. zorin
  64160. latypova
  64161. zlomskii
  64162. review
  64163. rakhmankulov
  64164. zorin
  64165. pastushenko
  64166. zlotsky
  64167. review
  64168. ramada
  64169. chenchaiah
  64170. chandra
  64171. kumar
  64172. krishna
  64173. review
  64174. ramadas
  64175. srinivasan
  64176. ramachandran
  64177. sastry
  64178. review
  64179. ramaiah
  64180. cyclopentannelltion
  64181. reactions
  64182. organic
  64183. review
  64184. randaccio
  64185. pahor
  64186. bresciani
  64187. zangrando
  64188. marzilli
  64189. review
  64190. rangansthan
  64191. ranganathan
  64192. bamezai
  64193. singh
  64194. review
  64195. paknikar
  64196. kirtane
  64197. recent
  64198. advnnces
  64199. review
  64200. rappoport
  64201. vinyl
  64202. cations
  64203. reactive
  64204. intermediates
  64205. review
  64206. rappoport
  64207. chemistry
  64208. enols
  64209. chemist
  64210. review
  64211. rasmussen
  64212. jerald
  64213. hellmann
  64214. steven
  64215. krepski
  64216. larry
  64217. review
  64218. rastogi
  64219. sharma
  64220. aminobenzimidazoles
  64221. organic
  64222. review
  64223. ratcliffe
  64224. albers
  64225. schonberg
  64226. penems
  64227. chemist
  64228. review
  64229. asymmetric
  64230. photochemistry
  64231. solution
  64232. review
  64233. raymond
  64234. kenneth
  64235. mcmurry
  64236. thomas
  64237. garrett
  64238. thomas
  64239. review
  64240. razvodovskaya
  64241. grapov
  64242. mel'nikov
  64243. phosphor
  64244. review
  64245. reactions
  64246. group
  64247. organobimetallic
  64248. compounds
  64249. review
  64250. rebek
  64251. binding
  64252. forces
  64253. equilibria
  64254. rates
  64255. review
  64256. rebek
  64257. recent
  64258. progress
  64259. molecular
  64260. recognition
  64261. review
  64262. rebek
  64263. julius
  64264. heterocycles
  64265. molecular
  64266. recognit
  64267. review
  64268. rebek
  64269. julius
  64270. model
  64271. studies
  64272. recognition
  64273. using
  64274. review
  64275. rebek
  64276. julius
  64277. molecular
  64278. recognition
  64279. biophysic
  64280. review
  64281. rebek
  64282. julius
  64283. molecular
  64284. recognition
  64285. model
  64286. review
  64287. rebek
  64288. julius
  64289. recognition
  64290. catalysis
  64291. using
  64292. review
  64293. recent
  64294. advances
  64295. field
  64296. heterosubstituted
  64297. review
  64298. recent
  64299. advances
  64300. enzymatic
  64301. degradation
  64302. review
  64303. recent
  64304. progess
  64305. manufacturing
  64306. technology
  64307. review
  64308. recent
  64309. progress
  64310. synthesis
  64311. reactivity
  64312. review
  64313. redpath
  64314. zeelen
  64315. stereoselective
  64316. synthesis
  64317. review
  64318. reetz
  64319. chelalion
  64320. chelation
  64321. control
  64322. review
  64323. reetz
  64324. lewis
  64325. induced
  64326. aikylation
  64327. carbon
  64328. review
  64329. reetz
  64330. organotitanium
  64331. reagents
  64332. organic
  64333. synthe
  64334. review
  64335. reetz
  64336. manfred
  64337. asymmetric
  64338. carbon
  64339. carbon
  64340. forma
  64341. review
  64342. regitz
  64343. short
  64344. lived
  64345. phosphorus
  64346. compounds
  64347. review
  64348. regitz
  64349. manfred
  64350. phosphaalkynes
  64351. building
  64352. blocks
  64353. review
  64354. rehacek
  64355. sajdl
  64356. ergot
  64357. alkaloids
  64358. chemistry
  64359. biologi
  64360. review
  64361. reichardt
  64362. christian
  64363. solvents
  64364. solvent
  64365. effects
  64366. review
  64367. photochemistry
  64368. nitrogen
  64369. containing
  64370. review
  64371. photochemistry
  64372. oxygen
  64373. sulfur
  64374. review
  64375. reider
  64376. roland
  64377. maytansinoids
  64378. alkaloids
  64379. review
  64380. reinecke
  64381. membered
  64382. hetarynes
  64383. reactive
  64384. inter
  64385. review
  64386. reinecke
  64387. hetarynes
  64388. tetrahedron
  64389. review
  64390. reinhoudt
  64391. thiepins
  64392. benzothiepins
  64393. conque
  64394. review
  64395. reissig
  64396. ulrich
  64397. donor
  64398. acceptor
  64399. substituted
  64400. review
  64401. remers
  64402. william
  64403. chemistry
  64404. antitumor
  64405. antibio
  64406. review
  64407. remnud
  64408. oberg
  64409. chattopadhyaya
  64410. synthesi
  64411. review
  64412. renfroe
  64413. harrington
  64414. proctor
  64415. azepines
  64416. review
  64417. retey
  64418. robinson
  64419. stereospecificity
  64420. organic
  64421. review
  64422. reutov
  64423. rearrangements
  64424. alkyl
  64425. radica
  64426. review
  64427. regitz
  64428. manfred
  64429. phosphaalkynes
  64430. building
  64431. blocks
  64432. review
  64433. reynolds
  64434. polar
  64435. substituent
  64436. effects
  64437. 198314165
  64438. review
  64439. robins
  64440. pyrrolizidine
  64441. alkaloids
  64442. 41115
  64443. review
  64444. rossi
  64445. roberto
  64446. pierini
  64447. adriana
  64448. palacios
  64449. review
  64450. russell
  64451. radical
  64452. reactions
  64453. involving
  64454. review
  64455. murai
  64456. ishida
  64457. proced
  64458. review
  64459. sammes
  64460. katritzky
  64461. pyrroles
  64462. review
  64463. santhanakrishnan
  64464. biohydroxlylation
  64465. terpenes
  64466. review
  64467. saxton
  64468. bisindole
  64469. alkaloids
  64470. alkaloids
  64471. review
  64472. schlosser
  64473. manfred
  64474. superbases
  64475. organic
  64476. synthesis
  64477. review
  64478. schurig
  64479. volker
  64480. nowotny
  64481. peter
  64482. chromatograph@
  64483. review
  64484. scriven
  64485. dialkylaminopyridine
  64486. super
  64487. acylatio@
  64488. review
  64489. serratosa
  64490. felix
  64491. organic
  64492. chemistry
  64493. action
  64494. review
  64495. wenqi
  64496. yingtai
  64497. chengji
  64498. synthes@
  64499. review
  64500. reynolds
  64501. polar
  64502. substituent
  64503. effects
  64504. 198314165
  64505. review
  64506. ricci
  64507. alfredo
  64508. degl'innocenti
  64509. alessandro
  64510. synthesis
  64511. review
  64512. richard
  64513. simple
  64514. relationships
  64515. between
  64516. carboca
  64517. review
  64518. richter
  64519. ulrich
  64520. membered
  64521. rings
  64522. review
  64523. rickborn
  64524. bruce
  64525. isobenzofurans
  64526. advances
  64527. theoretic
  64528. review
  64529. rideout
  64530. henry
  64531. beacham
  64532. nucleosid
  64533. review
  64534. heinz
  64535. membered
  64536. rings
  64537. containing
  64538. review
  64539. rieke
  64540. reuben
  64541. prepartion
  64542. organometallic
  64543. compoun
  64544. review
  64545. rinaldi
  64546. determination
  64547. absolute
  64548. configura
  64549. review
  64550. ripka
  64551. william
  64552. blaney
  64553. jeffrey
  64554. computer
  64555. graphics
  64556. review
  64557. ripperger
  64558. schreiber
  64559. nicotianamine
  64560. analogous
  64561. review
  64562. roberts
  64563. vellaccio
  64564. unusual
  64565. amino
  64566. acids
  64567. review
  64568. roberts
  64569. khalaf
  64570. friedel
  64571. crafts
  64572. alkylation
  64573. review
  64574. roberts
  64575. biotransformations
  64576. relating
  64577. heterocy
  64578. review
  64579. roberts
  64580. synthetic
  64581. routes
  64582. prostaglandins
  64583. review
  64584. robins
  64585. pyrrolizidine
  64586. alkaloids
  64587. 41115
  64588. review
  64589. robins
  64590. nucleoside
  64591. nucleotide
  64592. inhibitors
  64593. review
  64594. robins
  64595. purine
  64596. nucleoside
  64597. cyclic
  64598. monophospha
  64599. review
  64600. robinson
  64601. fischer
  64602. indole
  64603. synthesis
  64604. wiley
  64605. inter
  64606. review
  64607. rocchi
  64608. glormani
  64609. glycoproteins
  64610. covalent
  64611. attachme
  64612. review
  64613. rodrigo
  64614. russell
  64615. progress
  64616. chemistry
  64617. isoben
  64618. review
  64619. roeske
  64620. kennedy
  64621. transporting
  64622. peptides
  64623. review
  64624. daniel
  64625. romine
  64626. jeffrey
  64627. midura
  64628. wanda
  64629. meyers
  64630. review
  64631. ronec
  64632. catalysis
  64633. alloys
  64634. hydrocarbon
  64635. reaction
  64636. review
  64637. rosenfeld
  64638. cyclophanes
  64639. cyclophanes
  64640. review
  64641. rosini
  64642. goffredo
  64643. ballini
  64644. roberto
  64645. petrini
  64646. marino
  64647. review
  64648. benzodiazepine
  64649. alkaloids
  64650. alkaloids
  64651. chemi
  64652. review
  64653. rossa
  64654. vogtle
  64655. synthesis
  64656. medio
  64657. macrocyclic
  64658. review
  64659. rossi
  64660. rossi
  64661. aromatic
  64662. substitution
  64663. review
  64664. rossi
  64665. phenomenon
  64666. radical
  64667. anion
  64668. fragmentation
  64669. review
  64670. rossi
  64671. roberto
  64672. pierini
  64673. adriana
  64674. palacios
  64675. review
  64676. brief
  64677. history
  64678. photoinduced
  64679. electron
  64680. review
  64681. heinz
  64682. magnetic
  64683. resonance
  64684. methods
  64685. review
  64686. roush
  64687. william
  64688. stereochemical
  64689. synthetic
  64690. studie
  64691. review
  64692. ferreira
  64693. direct
  64694. biomimetic
  64695. synthesis
  64696. review
  64697. rozovskii
  64698. contemporary
  64699. problems
  64700. methanol
  64701. review
  64702. rozwadowska
  64703. secoisoquinoline
  64704. alkaloids
  64705. review
  64706. ruasse
  64707. marie
  64708. francoise
  64709. bromonium
  64710. bromocar
  64711. review
  64712. rubinovitz
  64713. willner
  64714. minsky
  64715. charged
  64716. review
  64717. rubottom
  64718. oxidations
  64719. tetraacetate
  64720. review
  64721. ruffing
  64722. charles
  64723. rhodium
  64724. catalyzed
  64725. hydroboration
  64726. review
  64727. runge
  64728. spectra
  64729. allenes
  64730. chemistry
  64731. allenes
  64732. review
  64733. runge
  64734. stereochemistry
  64735. allenes
  64736. chemistry
  64737. review
  64738. runge
  64739. substituent
  64740. effects
  64741. allenes
  64742. cumulene
  64743. review
  64744. russell
  64745. radical
  64746. chain
  64747. reactions
  64748. involvi
  64749. review
  64750. russell
  64751. radical
  64752. reactions
  64753. involving
  64754. review
  64755. ryabov
  64756. alexander
  64757. mechanisms
  64758. intramolecular
  64759. review
  64760. rzaev
  64761. coordination
  64762. effects
  64763. formation
  64764. review
  64765. rzeszotarska
  64766. barbara
  64767. masiukiewicz
  64768. elzbieta
  64769. arginine
  64770. review
  64771. chandrasekhar
  64772. product
  64773. review
  64774. eguchi
  64775. okano
  64776. takeuchi
  64777. heterocycles
  64778. review
  64779. nelsen
  64780. cation
  64781. radical
  64782. review
  64783. davies
  64784. synthesi
  64785. review
  64786. grasso
  64787. zappala
  64788. chimirri
  64789. heterocycles
  64790. review
  64791. gronowitz
  64792. wiley
  64793. chemistry
  64794. review
  64795. itsuno
  64796. synth
  64797. catalytic
  64798. review
  64799. blunden
  64800. cusack
  64801. smith
  64802. organomet
  64803. review
  64804. danishefsky
  64805. aldrichimica
  64806. reflec
  64807. review
  64808. danishefsky
  64809. deninno
  64810. angew
  64811. review
  64812. murai
  64813. ishida
  64814. proced
  64815. review
  64816. rajeswari
  64817. heterocycles
  64818. synthese
  64819. review
  64820. saraf
  64821. omran
  64822. saleh
  64823. heterocycles
  64824. review
  64825. suzuki
  64826. synth
  64827. review
  64828. sadekov
  64829. maksimenko
  64830. minkin
  64831. peculiarities
  64832. review
  64833. saegusa
  64834. developments
  64835. polymer
  64836. synthesis
  64837. review
  64838. saeva
  64839. photoinduced
  64840. electron
  64841. transfer
  64842. review
  64843. sakamoto
  64844. takao
  64845. kondo
  64846. yoshinori
  64847. yamanaka
  64848. hiroshi
  64849. review
  64850. sakata
  64851. gozyo
  64852. makino
  64853. kenji
  64854. kurasawa
  64855. yoshihisa
  64856. recent
  64857. review
  64858. salaun
  64859. cyclopropanone
  64860. hemiacetals
  64861. review
  64862. salaun
  64863. jacques
  64864. optically
  64865. active
  64866. cyclopropanes
  64867. review
  64868. salaun
  64869. jacques
  64870. synthesis
  64871. synthetic
  64872. applicat
  64873. review
  64874. salem
  64875. electrons
  64876. chemical
  64877. reactions
  64878. first
  64879. princ
  64880. review
  64881. salomon
  64882. homogeneous
  64883. metal
  64884. catalysis
  64885. organic
  64886. review
  64887. salter
  64888. heteronuclear
  64889. cluster
  64890. chemistry
  64891. review
  64892. sammes
  64893. katritzky
  64894. pyrroles
  64895. review
  64896. sammes
  64897. katritzky
  64898. lmidazoles
  64899. review
  64900. sammes
  64901. katritzky
  64902. pyrazoles
  64903. review
  64904. sammes
  64905. katritzky
  64906. lmidazoles
  64907. review
  64908. sammes
  64909. katritzky
  64910. pyrazoles
  64911. review
  64912. samuelsson
  64913. leukotrienes
  64914. highly
  64915. biologically
  64916. review
  64917. samuilov
  64918. konovalov
  64919. reactivity
  64920. adden
  64921. review
  64922. sander
  64923. wolfram
  64924. zwitterions
  64925. diradicals
  64926. review
  64927. sanders
  64928. mersh
  64929. nuclear
  64930. magnetic
  64931. double
  64932. review
  64933. sandler
  64934. stanley
  64935. organic
  64936. functional
  64937. review
  64938. sandstrom
  64939. dynamic
  64940. spectroscopy
  64941. academic
  64942. press
  64943. review
  64944. sandstrom
  64945. static
  64946. dynamic
  64947. stereochemistry
  64948. review
  64949. sannigrabi
  64950. niyogi
  64951. hobza
  64952. pavel
  64953. review
  64954. santelli
  64955. rouvier
  64956. santelli
  64957. nazarov
  64958. cyclizati
  64959. review
  64960. santhanakrishnan
  64961. biohydroxlylation
  64962. terpenes
  64963. review
  64964. santhanakrishnan
  64965. biohydroxlylation
  64966. terpenes
  64967. review
  64968. sappa
  64969. enrico
  64970. tiripicchio
  64971. antonio
  64972. stroll
  64973. review
  64974. saraf
  64975. mousawi
  64976. absorption
  64977. spectra
  64978. review
  64979. saraf
  64980. mousawi
  64981. infrared
  64982. spectra
  64983. review
  64984. saraf
  64985. mousawi
  64986. proton
  64987. magnetic
  64988. reson
  64989. review
  64990. sargent
  64991. stransky
  64992. dibenzofurans
  64993. review
  64994. sarkar
  64995. tarun
  64996. methods
  64997. synthesis
  64998. allylsi
  64999. review
  65000. sasaki
  65001. heteroadamantane
  65002. advances
  65003. review
  65004. satchell
  65005. derek
  65006. satchell
  65007. rosemary
  65008. mechanisms
  65009. review
  65010. satge
  65011. multiply
  65012. bonded
  65013. germanium
  65014. species
  65015. review
  65016. reactions
  65017. elemental
  65018. sulfur
  65019. activated
  65020. review
  65021. tadashi
  65022. anionic
  65023. organotin
  65024. compounds
  65025. organic
  65026. review
  65027. sauvage
  65028. pierre
  65029. interlacing
  65030. molecular
  65031. threads
  65032. review
  65033. saveant
  65034. michel
  65035. single
  65036. electron
  65037. transfer
  65038. review
  65039. saxton
  65040. bisindole
  65041. alkaloids
  65042. alkaloids
  65043. review
  65044. saxton
  65045. bisindole
  65046. alkaloids
  65047. alkaloids
  65048. review
  65049. saxton
  65050. indoles
  65051. monoterpenoid
  65052. indole
  65053. alkaloid
  65054. review
  65055. scaiano
  65056. handbook
  65057. organic
  65058. photochemist
  65059. review
  65060. scaiano
  65061. johnston
  65062. photochemistry
  65063. reaction
  65064. review
  65065. scaiano
  65066. laser
  65067. flash
  65068. photolysis
  65069. studies
  65070. review
  65071. scalsno
  65072. wintgens
  65073. netto
  65074. ferreira
  65075. mechanist
  65076. review
  65077. schaefer
  65078. silicon
  65079. carbon
  65080. double
  65081. review
  65082. schafer
  65083. jurgen
  65084. recent
  65085. contributions
  65086. kolbe
  65087. review
  65088. schaumann
  65089. ketcham
  65090. cycloreversions
  65091. review
  65092. scheffold
  65093. modern
  65094. synthetic
  65095. methods
  65096. spring
  65097. review
  65098. scheffold
  65099. transition
  65100. metals
  65101. organic
  65102. synthes
  65103. review
  65104. scheinmann
  65105. introduction
  65106. nomenclature
  65107. biosynth
  65108. review
  65109. scherer
  65110. complexes
  65111. substituent
  65112. review
  65113. schick
  65114. eichhorn
  65115. syntheses
  65116. reactions
  65117. review
  65118. schildknecht
  65119. turgorins
  65120. hormones
  65121. oftheendogeneous
  65122. review
  65123. schlosser
  65124. manfred
  65125. superbases
  65126. organic
  65127. synthesis
  65128. review
  65129. schmidt
  65130. richard
  65131. recent
  65132. developments
  65133. synthe
  65134. review
  65135. schon
  65136. sodium
  65137. liquid
  65138. ammonia
  65139. reduction
  65140. peptide
  65141. review
  65142. schoofs
  65143. guette
  65144. competitive
  65145. reaction
  65146. methods
  65147. review
  65148. schubert
  65149. solid
  65150. state
  65151. structures
  65152. carbene
  65153. comple
  65154. review
  65155. schuetz
  65156. benzodiazepines
  65157. handbook
  65158. springer
  65159. review
  65160. schultz
  65161. molecular
  65162. rearrangements
  65163. occurring
  65164. review
  65165. schultz
  65166. motyka
  65167. photochemical
  65168. heterocyclizatio
  65169. review
  65170. schultz
  65171. photochemical
  65172. electron
  65173. heterocycliz
  65174. review
  65175. schultz
  65176. arthur
  65177. enantioselective
  65178. methods
  65179. chira
  65180. review
  65181. schultz
  65182. arthur
  65183. photochemistry
  65184. cyclohexa
  65185. review
  65186. schulz
  65187. peter
  65188. catalytic
  65189. antibodies
  65190. review
  65191. schumann
  65192. organolanthanoid
  65193. compounds
  65194. review
  65195. schurig
  65196. chromatographic
  65197. methods
  65198. asymmetric
  65199. review
  65200. schurig
  65201. chromatographic
  65202. separation
  65203. enantio
  65204. review
  65205. schurig
  65206. volker
  65207. nowotny
  65208. peter
  65209. chromatograph
  65210. review
  65211. schuster
  65212. chemically
  65213. initiated
  65214. electron
  65215. review
  65216. schuster
  65217. schmidt
  65218. chemiluminescence
  65219. organ
  65220. review
  65221. schuster
  65222. coppola
  65223. allenes
  65224. organic
  65225. synthes
  65226. review
  65227. schwab
  65228. henderson
  65229. barry
  65230. enzyme
  65231. catalyzed
  65232. review
  65233. schwartz
  65234. jeffrey
  65235. arvanitis
  65236. georgia
  65237. smegel
  65238. review
  65239. schwarz
  65240. radical
  65241. eliminations
  65242. gaseous
  65243. cation
  65244. review
  65245. schwarz
  65246. helmut
  65247. generation
  65248. elusive
  65249. neutrals
  65250. review
  65251. schwarz
  65252. helmut
  65253. remote
  65254. functionalization
  65255. review
  65256. scolastico
  65257. carlo
  65258. asymmetric
  65259. synthesis
  65260. norephedr
  65261. review
  65262. scott
  65263. applications
  65264. molecular
  65265. biolo
  65266. review
  65267. scott
  65268. readily
  65269. available
  65270. chiral
  65271. carbon
  65272. fragments
  65273. review
  65274. scott
  65275. enantioselective
  65276. synthesis
  65277. review
  65278. scott
  65279. thermal
  65280. rearrangement
  65281. aromatic
  65282. compoun
  65283. review
  65284. screttas
  65285. constantinos
  65286. steele
  65287. barry
  65288. organometall
  65289. review
  65290. scriven
  65291. dialkylaminopyridine
  65292. super
  65293. acylatio
  65294. review
  65295. scriven
  65296. solution
  65297. chemistry
  65298. nitrenes
  65299. review
  65300. scriven
  65301. azides
  65302. nitrenes
  65303. reactivity
  65304. review
  65305. seebach
  65306. prelog
  65307. unambiguous
  65308. specification
  65309. review
  65310. seebach
  65311. dieter
  65312. organic
  65313. synthesis
  65314. where
  65315. review
  65316. seeman
  65317. effect
  65318. conformational
  65319. change
  65320. react
  65321. review
  65322. seeman
  65323. recent
  65324. studies
  65325. nicotine
  65326. chemistry
  65327. review
  65328. seevers
  65329. counsell
  65330. radioiodination
  65331. techniques
  65332. review
  65333. sellergren
  65334. boerje
  65335. molecular
  65336. imprinting
  65337. noncovale
  65338. review
  65339. semmelhack
  65340. chung
  65341. zhang
  65342. bodurow
  65343. sanner
  65344. review
  65345. seoane
  65346. carlos
  65347. teaching
  65348. organic
  65349. synthesis
  65350. review
  65351. seppelt
  65352. konrad
  65353. schmuck
  65354. structure
  65355. bonding
  65356. review
  65357. serebryakov
  65358. nguyen
  65359. mavrov
  65360. chiral
  65361. review
  65362. sergeev
  65363. smirnov
  65364. rostovshchikova
  65365. hydroch
  65366. review
  65367. serratosa
  65368. acetylene
  65369. diethers
  65370. logal
  65371. entry
  65372. review
  65373. serratosa
  65374. felix
  65375. organic
  65376. chemistry
  65377. action
  65378. review
  65379. servi
  65380. stefano
  65381. bakers
  65382. yeast
  65383. reagent
  65384. organic
  65385. review
  65386. otake
  65387. spectra
  65388. polyether
  65389. antibio
  65390. review
  65391. otake
  65392. spectra
  65393. polyether
  65394. review
  65395. seyden
  65396. penne
  65397. jacqueline
  65398. lithium
  65399. coordination
  65400. review
  65401. seymour
  65402. raymond
  65403. carraher
  65404. charles
  65405. giant
  65406. molecule
  65407. review
  65408. shaban
  65409. mohammed
  65410. synthesis
  65411. conden
  65412. review
  65413. shafran
  65414. bakulev
  65415. mokrushin
  65416. synthesis
  65417. review
  65418. shambayati
  65419. soroosh
  65420. crowe
  65421. william
  65422. schreiber
  65423. stuart
  65424. review
  65425. shamma
  65426. guinaudeau
  65427. biogenetic
  65428. pathways
  65429. review
  65430. shanzer
  65431. libman
  65432. frolow
  65433. macrocyclic
  65434. carbonyl
  65435. review
  65436. sharma
  65437. satyavan
  65438. isothiocyanates
  65439. heterocyclic
  65440. review
  65441. shawali
  65442. reactions
  65443. hydrazidoyl
  65444. halides
  65445. review
  65446. shchegolev
  65447. kanishchev
  65448. rearrangements
  65449. review
  65450. sheldon
  65451. roger
  65452. industrial
  65453. synthesis
  65454. optically
  65455. review
  65456. wenqi
  65457. yingtai
  65458. chengji
  65459. synthes
  65460. review
  65461. sheng
  65462. rongqin
  65463. rapid
  65464. recognize
  65465. kekulean
  65466. review
  65467. sheppard
  65468. automation
  65469. peptide
  65470. synthesis
  65471. review
  65472. sherrington
  65473. hodge
  65474. syntheses
  65475. separations
  65476. review
  65477. shida
  65478. haselbach
  65479. bally
  65480. organic
  65481. radical
  65482. review
  65483. shimizu
  65484. kamiya
  65485. bioactive
  65486. marine
  65487. biopolymers
  65488. review
  65489. shimizu
  65490. paralytic
  65491. shellfish
  65492. poisons
  65493. review
  65494. shimomura
  65495. mechanism
  65496. bioluminescence
  65497. chemical
  65498. review
  65499. stereoselective
  65500. synthesis
  65501. geometric
  65502. review
  65503. shine
  65504. henry
  65505. reflections
  65506. complex
  65507. theory
  65508. review
  65509. shinkai
  65510. manabe
  65511. photocontrol
  65512. extraction
  65513. review
  65514. shioiri
  65515. takayuki
  65516. hamada
  65517. yasumasa
  65518. natural
  65519. product
  65520. review
  65521. shklover
  65522. nagapetyan
  65523. stuchkov
  65524. struc
  65525. review
  65526. shklover
  65527. struchkov
  65528. voronkov
  65529. organosili
  65530. review
  65531. shkol'nikova
  65532. porai
  65533. koshits
  65534. stmcture
  65535. review
  65536. shockman
  65537. daneo
  65538. moore
  65539. mcdowell
  65540. review
  65541. shono
  65542. electroorganic
  65543. chemistry
  65544. organic
  65545. synthes
  65546. review
  65547. shono
  65548. tatsuya
  65549. synthesis
  65550. alkaloidal
  65551. compounds
  65552. review
  65553. shorter
  65554. hammett
  65555. memorial
  65556. lecture
  65557. 1990171
  65558. review
  65559. shteingarts
  65560. polyfluorinated
  65561. arenonium
  65562. review
  65563. shubin
  65564. rearrangements
  65565. carbocations
  65566. 12shif
  65567. review
  65568. shvachkin
  65569. mishin
  65570. korhsunova
  65571. advances
  65572. review
  65573. siebert
  65574. walter
  65575. polydecker
  65576. sandwich
  65577. complexes
  65578. review
  65579. siedle
  65580. solid
  65581. state
  65582. chemistry
  65583. molecular
  65584. metal
  65585. review
  65586. sigel
  65587. hydrophobic
  65588. metal
  65589. coordinating
  65590. review
  65591. sigel
  65592. lithium
  65593. halocarbenoids
  65594. carbanions
  65595. review
  65596. microbial
  65597. asymmetric
  65598. catalysis
  65599. review
  65600. charles
  65601. hsiung
  65602. resolution
  65603. enantiom
  65604. review
  65605. silverstein
  65606. bassler
  65607. clayton
  65608. morrill
  65609. terence
  65610. review
  65611. silwa
  65612. substituted
  65613. pyridinium
  65614. salts
  65615. review
  65616. shockman
  65617. daneo
  65618. moore
  65619. mcdowell
  65620. review
  65621. simchen
  65622. chemistry
  65623. trialkylsilyl
  65624. perfluoralkane@
  65625. review
  65626. sliwa
  65627. chemistry
  65628. furazans
  65629. 221571
  65630. heter@
  65631. review
  65632. solladie
  65633. cavallo
  65634. arlette
  65635. chiral
  65636. arene
  65637. chromium
  65638. carb@
  65639. review
  65640. stanek
  65641. preparation
  65642. selectively
  65643. alkylated
  65644. review
  65645. stock
  65646. pyrolysis
  65647. revi@
  65648. review
  65649. sugimoto
  65650. toyonari
  65651. yoshida
  65652. zenichi
  65653. overall
  65654. review
  65655. suzuki
  65656. constituents
  65657. pepper
  65658. species
  65659. review
  65660. boivin
  65661. tetrahedron
  65662. tetrahedron
  65663. review
  65664. takagi
  65665. crown
  65666. compounds
  65667. alkali
  65668. alkal@
  65669. review
  65670. taylor
  65671. synthesis
  65672. analogues
  65673. prostaglandi@
  65674. review
  65675. thayer
  65676. organometallic
  65677. compounds
  65678. living
  65679. orga@
  65680. review
  65681. tiecco
  65682. testaferri
  65683. homolytic
  65684. aromatic
  65685. substituti@
  65686. review
  65687. tominaga
  65688. yoshinori
  65689. kohra
  65690. shinya
  65691. honkawa
  65692. harumasa
  65693. review
  65694. simchen
  65695. chemistry
  65696. trialkylsilyl
  65697. perfluoralkane
  65698. review
  65699. simon
  65700. peters
  65701. picosecond
  65702. studies
  65703. organic
  65704. review
  65705. simonetta
  65706. organic
  65707. reaction
  65708. paths
  65709. theoretical
  65710. review
  65711. simons
  65712. stereodynamics
  65713. molecular
  65714. photodissoci
  65715. review
  65716. simpkins
  65717. stereoselective
  65718. reactions
  65719. organ
  65720. review
  65721. simpkins
  65722. nigel
  65723. chemistry
  65724. vinyl
  65725. sulfones
  65726. review
  65727. lewis
  65728. order
  65729. methods
  65730. calculati
  65731. review
  65732. sinev
  65733. korchak
  65734. krylov
  65735. mechanism
  65736. review
  65737. singaram
  65738. addition
  65739. compounds
  65740. boron
  65741. review
  65742. singleton
  65743. oosthuizen
  65744. metal
  65745. isocyanide
  65746. comple
  65747. review
  65748. sinnott
  65749. michael
  65750. principle
  65751. least
  65752. nuclear
  65753. review
  65754. sinyashin
  65755. batyeva
  65756. pudovik
  65757. progress
  65758. review
  65759. skancke
  65760. effect
  65761. fluorine
  65762. substituent
  65763. review
  65764. skell
  65765. traynham
  65766. radical
  65767. brominations
  65768. review
  65769. slivinskii
  65770. voitsekhovskii
  65771. development
  65772. review
  65773. sliwa
  65774. chemistry
  65775. furazans
  65776. 221571
  65777. heter
  65778. review
  65779. sliwa
  65780. thomas
  65781. fused
  65782. thiadiazoles
  65783. selenad
  65784. review
  65785. smadja
  65786. electrophilic
  65787. addition
  65788. allenic
  65789. derivati
  65790. review
  65791. sinta
  65792. macroheterocyclic
  65793. ligands
  65794. polymer
  65795. review
  65796. smith
  65797. salicylidenamino
  65798. chirality
  65799. review
  65800. smith
  65801. synthetically
  65802. useful
  65803. reactions
  65804. epoxide
  65805. review
  65806. smith
  65807. janice
  65808. fieser
  65809. fieser
  65810. fieser's
  65811. review
  65812. smith
  65813. keith
  65814. controlled
  65815. organic
  65816. synthesis
  65817. review
  65818. smith
  65819. michael
  65820. dienyl
  65821. amides
  65822. lactams
  65823. prepara
  65824. review
  65825. smith
  65826. mitchell
  65827. dooseop
  65828. horenstein
  65829. benjamin
  65830. review
  65831. snieckus
  65832. regioselective
  65833. synthetic
  65834. processes
  65835. based
  65836. review
  65837. snieckus
  65838. directed
  65839. ortho
  65840. metalation
  65841. reaction
  65842. review
  65843. snieckus
  65844. victor
  65845. directed
  65846. ortho
  65847. metalation
  65848. tertiary
  65849. review
  65850. sobenina
  65851. mikhaleva
  65852. trofimov
  65853. synthesis
  65854. review
  65855. sokolovskii
  65856. yur'eva
  65857. matros
  65858. review
  65859. solladie
  65860. cavallo
  65861. arlette
  65862. chiral
  65863. arene
  65864. chromium
  65865. review
  65866. solladie
  65867. addition
  65868. chiral
  65869. nucleophiles
  65870. aldeh
  65871. review
  65872. solladie
  65873. zimmermann
  65874. liquid
  65875. crystals
  65876. review
  65877. solladie
  65878. recent
  65879. results
  65880. field
  65881. asymmet
  65882. review
  65883. novel
  65884. molecule
  65885. chemistry
  65886. within
  65887. vanderwaal
  65888. review
  65889. sorrell
  65890. thomas
  65891. synthetic
  65892. models
  65893. binuclear
  65894. review
  65895. southon
  65896. buckingham
  65897. dictionary
  65898. alkaloid
  65899. review
  65900. spatola
  65901. peptide
  65902. backbone
  65903. modifications
  65904. struct
  65905. review
  65906. sporn
  65907. goodman
  65908. retinoids
  65909. volumes
  65910. review
  65911. clair
  65912. black
  65913. david
  65914. kumar
  65915. naresh
  65916. pyrroloquinolines
  65917. review
  65918. stable
  65919. isotopically
  65920. enriched
  65921. glucose
  65922. strategies
  65923. review
  65924. stahl
  65925. quarter
  65926. century
  65927. layer
  65928. chromatogra
  65929. review
  65930. staley
  65931. carbanions
  65932. reactive
  65933. intermediates
  65934. review
  65935. stammer
  65936. dehydroamino
  65937. acids
  65938. proteins
  65939. chemist
  65940. review
  65941. stammer
  65942. charles
  65943. cyclopropane
  65944. amino
  65945. acids
  65946. review
  65947. stanek
  65948. preparation
  65949. selectively
  65950. alkylated
  65951. review
  65952. stang
  65953. hanack
  65954. subramanian
  65955. perfluoroalkanes
  65956. review
  65957. stang
  65958. recent
  65959. developments
  65960. unsaturated
  65961. carben
  65962. review
  65963. stang
  65964. white
  65965. triflic
  65966. derivative
  65967. review
  65968. starodub
  65969. krivoshei
  65970. highly
  65971. anisotropic
  65972. molec
  65973. review
  65974. wadsworth
  65975. emmons
  65976. reaction
  65977. revisited
  65978. review
  65979. wojciech
  65980. opportunities
  65981. bioorganic
  65982. review
  65983. steggerda
  65984. velden
  65985. prepara
  65986. review
  65987. steglich
  65988. wolfgang
  65989. strack
  65990. dieter
  65991. betalains
  65992. alkal
  65993. review
  65994. stella
  65995. homolytic
  65996. cyclization
  65997. chloroalkenylam
  65998. review
  65999. stephenson
  66000. david
  66001. linear
  66002. prediction
  66003. maximum
  66004. review
  66005. stevens
  66006. nucleophilic
  66007. additions
  66008. tetrahydropyr
  66009. review
  66010. stevenson
  66011. wilson
  66012. chiral
  66013. separations
  66014. plenu
  66015. review
  66016. stewart
  66017. arnett
  66018. chiral
  66019. monolayers
  66020. review
  66021. stock
  66022. wasielewski
  66023. trifluoromethyl
  66024. group
  66025. review
  66026. stock
  66027. pyrolysis
  66028. review
  66029. stoddard
  66030. fraser
  66031. molecular
  66032. review
  66033. stoddart
  66034. fraaer
  66035. third
  66036. allotropic
  66037. review
  66038. stoddart
  66039. fraser
  66040. conception
  66041. birth
  66042. recep
  66043. review
  66044. stoddart
  66045. fraser
  66046. zarzycki
  66047. ryszard
  66048. cyclodextrins
  66049. review
  66050. stork
  66051. survey
  66052. radical
  66053. mediated
  66054. cyclizatio
  66055. review
  66056. stout
  66057. meyers
  66058. recent
  66059. advances
  66060. chemist
  66061. review
  66062. stowell
  66063. three
  66064. carbon
  66065. homologating
  66066. agents
  66067. review
  66068. strazewski
  66069. peter
  66070. christoph
  66071. replication
  66072. experim
  66073. review
  66074. strazzolini
  66075. paolo
  66076. giumanini
  66077. angelo
  66078. cauci
  66079. sabina
  66080. review
  66081. streitwieser
  66082. carbanion
  66083. pairs
  66084. triplets
  66085. review
  66086. studies
  66087. oxacephems
  66088. artifcial
  66089. review
  66090. suami
  66091. tetsuo
  66092. chemistry
  66093. pseudo
  66094. sugars
  66095. 1990154
  66096. review
  66097. suami
  66098. tetsuo
  66099. ogawa
  66100. seiichiro
  66101. chemistry
  66102. carba
  66103. review
  66104. sucrow
  66105. reactions
  66106. acetylenes
  66107. hydrazines
  66108. review
  66109. sugimoto
  66110. toyonari
  66111. yoshida
  66112. zenichi
  66113. overall
  66114. review
  66115. summers
  66116. bipyridines
  66117. advances
  66118. review
  66119. sundberg
  66120. chloroacetamide
  66121. photocyclizations
  66122. review
  66123. sunko
  66124. hehre
  66125. secondary
  66126. deuterium
  66127. isotope
  66128. review
  66129. surpateanu
  66130. lablache
  66131. combier
  66132. reactivity
  66133. cyclo
  66134. review
  66135. surzur
  66136. cyclizations
  66137. intramolecular
  66138. additions
  66139. review
  66140. surzur
  66141. marie
  66142. bertrand
  66143. michele
  66144. paula
  66145. lactone
  66146. review
  66147. sustman
  66148. reiner
  66149. korth
  66150. captodative
  66151. review
  66152. sutherland
  66153. cyclophanes
  66154. synthetic
  66155. analogues
  66156. review
  66157. sutherland
  66158. cyclophanes
  66159. synthetic
  66160. receptors
  66161. review
  66162. sutherland
  66163. synthetic
  66164. ditopic
  66165. receptors
  66166. advanc
  66167. review
  66168. suzuki
  66169. organoborates
  66170. synthetic
  66171. reactions
  66172. review
  66173. suzuki
  66174. aspects
  66175. organic
  66176. synthesis
  66177. using
  66178. review
  66179. suzuki
  66180. akira
  66181. haloboration
  66182. application
  66183. review
  66184. suzuki
  66185. akira
  66186. synthetic
  66187. studies
  66188. cross
  66189. coupli
  66190. review
  66191. suzuki
  66192. constituents
  66193. pepper
  66194. species
  66195. review
  66196. sveda
  66197. galaev
  66198. enzymic
  66199. conversion
  66200. racemates
  66201. review
  66202. swenton
  66203. quinone
  66204. monoketals
  66205. electroc
  66206. review
  66207. sykes
  66208. physiology
  66209. biochemistry
  66210. inacti
  66211. review
  66212. synthesis
  66213. 1abeled
  66214. steroid
  66215. hormones
  66216. zomer
  66217. review
  66218. synthetic
  66219. procedures
  66220. preparation
  66221. deuteri
  66222. review
  66223. synthetic
  66224. transformations
  66225. using
  66226. arenesulfonyloxy
  66227. review
  66228. szantay
  66229. csaba
  66230. indole
  66231. alkaloids
  66232. human
  66233. medicine
  66234. review
  66235. szeimies
  66236. bridgehead
  66237. olefins
  66238. reactive
  66239. intermediate
  66240. review
  66241. szele
  66242. zollinger
  66243. coupling
  66244. reactions
  66245. structur
  66246. review
  66247. o'donnell
  66248. stabilization
  66249. review
  66250. hirao
  66251. ohshiro
  66252. synth
  66253. review
  66254. simpson
  66255. applications
  66256. review
  66257. katsuki
  66258. synth
  66259. recent
  66260. review
  66261. kitazume
  66262. yamazaki
  66263. synth
  66264. review
  66265. boivin
  66266. tetrahedron
  66267. tetrahedron
  66268. review
  66269. romney
  66270. alexander
  66271. heterocycles
  66272. review
  66273. mitsudo
  66274. watanabe
  66275. organomet
  66276. review
  66277. mukaiyama
  66278. murakami
  66279. synthesis
  66280. review
  66281. nagahara
  66282. kametani
  66283. heterocycles
  66284. review
  66285. ohmaye
  66286. synth
  66287. review
  66288. review
  66289. suami
  66290. synthetic
  66291. ventu
  66292. review
  66293. bastock
  66294. synthetic
  66295. review
  66296. taber
  66297. intramolecular
  66298. diels
  66299. alder
  66300. alder
  66301. review
  66302. tabushi
  66303. cyclodextrin
  66304. catalysis
  66305. model
  66306. review
  66307. tabushi
  66308. design
  66309. synthesis
  66310. artificial
  66311. enzyme
  66312. review
  66313. tabushi
  66314. kuroda
  66315. cyclodextrins
  66316. cyclophanes
  66317. review
  66318. tabushi
  66319. yamamura
  66320. water
  66321. soluble
  66322. cyclophanes
  66323. review
  66324. tacke
  66325. design
  66326. substitution
  66327. microb
  66328. review
  66329. protonic
  66330. acidities
  66331. basicities
  66332. review
  66333. takagi
  66334. crown
  66335. compounds
  66336. alkali
  66337. alkal
  66338. review
  66339. takahata
  66340. hiroki
  66341. yamazaki
  66342. takao
  66343. synthesis
  66344. heteroc
  66345. review
  66346. takano
  66347. ogasawara
  66348. alkaloids
  66349. calabar
  66350. review
  66351. takeda
  66352. solvent
  66353. extraction
  66354. metal
  66355. review
  66356. takeuchi
  66357. yoshio
  66358. chemistry
  66359. multifunctional
  66360. carbon
  66361. review
  66362. christoph
  66363. jeker
  66364. nicolas
  66365. synthesis
  66366. macrocycl
  66367. review
  66368. tanaka
  66369. masato
  66370. sakakura
  66371. toshiyasu
  66372. photocatalytic
  66373. review
  66374. tanaka
  66375. masato
  66376. activate
  66377. irradiate
  66378. review
  66379. reactions
  66380. silicon
  66381. atoms
  66382. silylenes
  66383. review
  66384. tarasova
  66385. moskva
  66386. cyclic
  66387. diphosphaze
  66388. review
  66389. tashner
  66390. michael
  66391. asymmetric
  66392. diels
  66393. alder
  66394. reactions
  66395. review
  66396. taube
  66397. electron
  66398. transfer
  66399. between
  66400. metal
  66401. complexes
  66402. review
  66403. taylor
  66404. chemistry
  66405. limonoids
  66406. review
  66407. taylor
  66408. carbenegs
  66409. carbenoids
  66410. neighborin
  66411. review
  66412. taylor
  66413. electrophilic
  66414. aromatic
  66415. substitution
  66416. wiley
  66417. review
  66418. taylor
  66419. synthesis
  66420. analogues
  66421. prostaglandi
  66422. review
  66423. taylor
  66424. synthesis
  66425. naturally
  66426. occurring
  66427. prost
  66428. review
  66429. taylor
  66430. synthesis
  66431. prostacyclin
  66432. analogu
  66433. review
  66434. taylor
  66435. synthesis
  66436. thromboxane
  66437. analogues
  66438. review
  66439. taylor
  66440. kennard
  66441. hydrogen
  66442. geometry
  66443. organi
  66444. review
  66445. tedder
  66446. importance
  66447. polarity
  66448. strength
  66449. review
  66450. tedder
  66451. which
  66452. factors
  66453. determine
  66454. reactivity
  66455. review
  66456. telrazolium
  66457. sults
  66458. zhivich
  66459. koldobskii
  66460. ostrovsk
  66461. review
  66462. tempe
  66463. chemistry
  66464. biochemistry
  66465. chain
  66466. review
  66467. templeton
  66468. joseph
  66469. electron
  66470. alkyne
  66471. ligands
  66472. review
  66473. terashima
  66474. masanao
  66475. ishikura
  66476. minoru
  66477. boron
  66478. substituted
  66479. review
  66480. terrier
  66481. equilibrium
  66482. studies
  66483. jackson
  66484. review
  66485. teuber
  66486. naturally
  66487. occurring
  66488. dithiolanes
  66489. review
  66490. thatcher
  66491. gregory
  66492. kluger
  66493. ronald
  66494. mechanism
  66495. review
  66496. thayer
  66497. brinhnan
  66498. biological
  66499. methylation
  66500. review
  66501. thayer
  66502. organometallic
  66503. compounds
  66504. living
  66505. review
  66506. chemistry
  66507. hydroxyindoles
  66508. their
  66509. derivat
  66510. review
  66511. synthesis
  66512. dithiolene
  66513. strong
  66514. review
  66515. theander
  66516. nelson
  66517. david
  66518. aqueous
  66519. temperatu
  66520. review
  66521. thebtaranonth
  66522. thebtaranonth
  66523. developments
  66524. review
  66525. theimer
  66526. benzene
  66527. derived
  66528. cyclic
  66529. carbinols
  66530. fragra
  66531. review
  66532. theopold
  66533. klaus
  66534. organochromium
  66535. chemistry
  66536. review
  66537. thibblin
  66538. ahlberg
  66539. reaction
  66540. branching
  66541. review
  66542. thiel
  66543. walter
  66544. semiempirical
  66545. methods
  66546. current
  66547. status
  66548. review
  66549. thiem
  66550. joachim
  66551. klaffke
  66552. werner
  66553. syntheses
  66554. deoxy
  66555. review
  66556. thummel
  66557. effect
  66558. strain
  66559. ortho
  66560. review
  66561. tidwell
  66562. destabilized
  66563. carbocations
  66564. review
  66565. tidwell
  66566. thomas
  66567. ketene
  66568. chemistry
  66569. second
  66570. golden
  66571. review
  66572. tidwell
  66573. thomas
  66574. oxidation
  66575. alcohols
  66576. activated
  66577. review
  66578. tidwell
  66579. thomas
  66580. oxidation
  66581. alcohols
  66582. carbonyl
  66583. review
  66584. tiecco
  66585. testaferri
  66586. homolytic
  66587. aromatic
  66588. substituti
  66589. review
  66590. timofeeva
  66591. struchkov
  66592. conformational
  66593. review
  66594. timokhin
  66595. structural
  66596. features
  66597. reactivity
  66598. review
  66599. timpe
  66600. el'tsov
  66601. pseudoazulenes
  66602. review
  66603. tisler
  66604. heterocyclic
  66605. amidines
  66606. hydroxyamidines
  66607. review
  66608. tisler
  66609. heterocyclic
  66610. quinones
  66611. review
  66612. tisler
  66613. stanovnik
  66614. branko
  66615. advances
  66616. pyridazine
  66617. review
  66618. tisler
  66619. syntheses
  66620. heterocycles
  66621. intramolec
  66622. review
  66623. tochtermann
  66624. werner
  66625. olsson
  66626. heteroquadricyclan
  66627. review
  66628. reaction
  66629. control
  66630. guest
  66631. compounds
  66632. review
  66633. fumio
  66634. modern
  66635. aspect
  66636. classical
  66637. aromatic
  66638. review
  66639. chemiluminescence
  66640. reactions
  66641. ozone
  66642. review
  66643. tolbert
  66644. photochemistry
  66645. organic
  66646. anions
  66647. review
  66648. tomasik
  66649. piotr
  66650. palasinski
  66651. mieczyslaw
  66652. wiejak
  66653. stanisla
  66654. review
  66655. tomasik
  66656. piotr
  66657. wiejak
  66658. stanislaw
  66659. palasinski
  66660. mieczysla
  66661. review
  66662. tominaga
  66663. yoshinori
  66664. kohra
  66665. shinya
  66666. honkawa
  66667. harumasa
  66668. review
  66669. tominaga
  66670. yoshinori
  66671. shiroshita
  66672. yoshihide
  66673. hosomi
  66674. review
  66675. tomioka
  66676. noncatalytic
  66677. additions
  66678. dunsat
  66679. review
  66680. tomioka
  66681. kiyoshi
  66682. asymmetric
  66683. synthesis
  66684. utilizing
  66685. review
  66686. tomoda
  66687. shuji
  66688. usuki
  66689. yoshinosuke
  66690. fujita
  66691. review
  66692. tonellato
  66693. uumberto
  66694. esterolytic
  66695. reactivity
  66696. micell
  66697. review
  66698. toone
  66699. simon
  66700. ethan
  66701. bednarski
  66702. whitesi
  66703. review
  66704. topsom
  66705. contribution
  66706. theoretical
  66707. chemistry
  66708. review
  66709. topsom
  66710. theoretical
  66711. studies
  66712. effects
  66713. review
  66714. torii
  66715. sigeru
  66716. tanaka
  66717. hideo
  66718. inokuchi
  66719. tsutomu
  66720. review
  66721. torsell
  66722. nitrile
  66723. oxides
  66724. nitrones
  66725. nitronate
  66726. review
  66727. touchstone
  66728. practice
  66729. layer
  66730. chromatograph
  66731. review
  66732. toullec
  66733. enolisation
  66734. simple
  66735. carbonyl
  66736. compounds
  66737. review
  66738. townsend
  66739. leroy
  66740. chemistry
  66741. nucleosides
  66742. review
  66743. tramontini
  66744. stereoselective
  66745. synthesis
  66746. diastereo
  66747. review
  66748. tramontini
  66749. maurilio
  66750. angiolini
  66751. luigi
  66752. further
  66753. advance
  66754. review
  66755. transformations
  66756. hydroxyalkyl
  66757. selenides
  66758. review
  66759. trass
  66760. advances
  66761. chemistry
  66762. interes
  66763. review
  66764. treger
  66765. rozanov
  66766. synthesis
  66767. organochlo
  66768. review
  66769. trofimov
  66770. prospects
  66771. chemistry
  66772. pyrrole
  66773. review
  66774. trofimov
  66775. boris
  66776. preparation
  66777. pyrroles
  66778. ketox
  66779. review
  66780. trogler
  66781. william
  66782. organometallic
  66783. radical
  66784. process
  66785. review
  66786. trogler
  66787. william
  66788. synthesis
  66789. electronic
  66790. structure
  66791. review
  66792. trost
  66793. cyclopentanoids
  66794. challenge
  66795. metho
  66796. review
  66797. trost
  66798. barry
  66799. cyclizations
  66800. palladium
  66801. catalyzed
  66802. review
  66803. trost
  66804. barry
  66805. palladium
  66806. catalyzed
  66807. cycloisomerizatio
  66808. review
  66809. trost
  66810. barry
  66811. transition
  66812. metal
  66813. templates
  66814. catalys
  66815. review
  66816. trost
  66817. barry
  66818. transition
  66819. metal
  66820. templates
  66821. guide
  66822. review
  66823. truce
  66824. cycloadducts
  66825. derived
  66826. sulfen
  66827. review
  66828. truce
  66829. william
  66830. forty
  66831. years
  66832. organosulfur
  66833. chemist
  66834. review
  66835. tramontini
  66836. maurilio
  66837. angiolini
  66838. luigi
  66839. further
  66840. advance@
  66841. review
  66842. tsuchiya
  66843. tsutomu
  66844. chemistry
  66845. developments
  66846. fluo@
  66847. review
  66848. bauer
  66849. johannes
  66850. baumgartner
  66851. regina
  66852. fontai@
  66853. review
  66854. vahrenkamp
  66855. heinrich
  66856. interconversions
  66857. review
  66858. vedejs
  66859. krafft
  66860. cyclic
  66861. sulfides
  66862. organic
  66863. synt@
  66864. review
  66865. vliegenihari
  66866. dorland
  66867. halbeek
  66868. review
  66869. neumann
  66870. synthesis
  66871. butyltin
  66872. hydri@
  66873. review
  66874. warner
  66875. philip
  66876. strained
  66877. bridgehead
  66878. double
  66879. bonds
  66880. review
  66881. weidmann
  66882. seebach
  66883. organometallic
  66884. compounds
  66885. review
  66886. werner
  66887. helmut
  66888. erker
  66889. gerhard
  66890. organometallics
  66891. review
  66892. wiberg
  66893. kenneth
  66894. small
  66895. propellanes
  66896. review
  66897. wilman
  66898. derry
  66899. chemistry
  66900. antitumor
  66901. review
  66902. arene
  66903. syntheses@
  66904. review
  66905. yamamoto
  66906. acyclic
  66907. stereoc@
  66908. review
  66909. tsuchiya
  66910. tsutomu
  66911. chemistry
  66912. developments
  66913. review
  66914. tsuge
  66915. kanemasa
  66916. recent
  66917. advances
  66918. azomethine
  66919. review
  66920. tsuji
  66921. synthetic
  66922. applications
  66923. palladium
  66924. review
  66925. tsuji
  66926. nishidu
  66927. thermal
  66928. opening
  66929. cycloadditio
  66930. review
  66931. turner
  66932. aldridge
  66933. fungal
  66934. metabolites
  66935. acade
  66936. review
  66937. turro
  66938. kraeutler
  66939. magnetic
  66940. isotope
  66941. effects
  66942. review
  66943. tvaroska
  66944. bleha
  66945. tomas
  66946. anomeric
  66947. anomeric
  66948. review
  66949. tvaroska
  66950. computational
  66951. methods
  66952. studying
  66953. review
  66954. tyuleneva
  66955. rokhlin
  66956. knunyants
  66957. fluorine
  66958. review
  66959. hacksell
  66960. hogberg
  66961. pharm
  66962. suecica
  66963. review
  66964. pindur
  66965. ortho
  66966. esters
  66967. review
  66968. uemura
  66969. motokazu
  66970. tricarbonyl
  66971. arene
  66972. chromium
  66973. compl
  66974. review
  66975. uemura
  66976. sakae
  66977. synthetic
  66978. utility
  66979. mcpba
  66980. oxidation
  66981. review
  66982. isocyanides
  66983. component
  66984. condensat
  66985. review
  66986. marquarding
  66987. urban
  66988. synthesis
  66989. peptid
  66990. review
  66991. bauer
  66992. johannes
  66993. baumgartner
  66994. regina
  66995. fontai
  66996. review
  66997. aspects
  66998. homogeneous
  66999. catalysis
  67000. review
  67001. uhlmann
  67002. eugen
  67003. peyman
  67004. anusch
  67005. antisense
  67006. oligonucleoti
  67007. review
  67008. undheim
  67009. kjell
  67010. benneche
  67011. metallation
  67012. metal
  67013. review
  67014. preassembled
  67015. fe/mo/si
  67016. clusters
  67017. review
  67018. rafael
  67019. miguel
  67020. synthetic
  67021. approaches
  67022. review
  67023. timokhina
  67024. voronov
  67025. synthesis
  67026. review
  67027. usyatinskii
  67028. bregadze
  67029. derivatives
  67030. review
  67031. bakulev
  67032. mokrushin
  67033. heterocycl
  67034. compd
  67035. review
  67036. dombrovskii
  67037. review
  67038. rawal
  67039. jones
  67040. heterocycles
  67041. review
  67042. dzhemilev
  67043. norbor
  67044. review
  67045. ramamurthy
  67046. venkatesan
  67047. review
  67048. ramamurthy
  67049. scheffer
  67050. turro
  67051. tetrahedron
  67052. review
  67053. vahrenkamp
  67054. basic
  67055. metal
  67056. cluster
  67057. reactions
  67058. review
  67059. vahrenkamp
  67060. heinrich
  67061. interconversions
  67062. review
  67063. valentine
  67064. preparation
  67065. enantiomers
  67066. review
  67067. valters
  67068. electronic
  67069. steric
  67070. effects
  67071. review
  67072. bekkum
  67073. kouwenhoven
  67074. zeolites
  67075. review
  67076. sande
  67077. diffusion
  67078. systems
  67079. color
  67080. review
  67081. wozniak
  67082. react
  67083. review
  67084. gunsteren
  67085. wilfred
  67086. berendsen
  67087. herman
  67088. comput
  67089. review
  67090. koten
  67091. vrieze
  67092. diaza
  67093. butadiene
  67094. diimin
  67095. review
  67096. koten
  67097. gerard
  67098. novel
  67099. aspects
  67100. diiodine
  67101. coordi
  67102. review
  67103. koten
  67104. gerard
  67105. tuning
  67106. reactivity
  67107. metals
  67108. review
  67109. adventures
  67110. excursions
  67111. bioassay
  67112. review
  67113. varezhkin
  67114. zhinkin
  67115. morgunova
  67116. struc
  67117. review
  67118. varvoglis
  67119. aryliodine
  67120. dicarboxylates
  67121. 198110
  67122. review
  67123. varvoglis
  67124. polyvalent
  67125. lodine
  67126. compounds
  67127. organic
  67128. review
  67129. vasella
  67130. andrea
  67131. baudin
  67132. gisele
  67133. panza
  67134. luigi
  67135. synthesis
  67136. review
  67137. vedejs
  67138. krafft
  67139. cyclic
  67140. sulfides
  67141. organic
  67142. review
  67143. vedejs
  67144. nonstabilized
  67145. azomethine
  67146. ylides
  67147. advances
  67148. review
  67149. vedejs
  67150. sufur
  67151. mediated
  67152. expansions
  67153. total
  67154. review
  67155. veith
  67156. alkyl
  67157. substituted
  67158. group
  67159. metal
  67160. review
  67161. veith
  67162. recktenwal
  67163. structure
  67164. reactivity
  67165. review
  67166. veith
  67167. michael
  67168. compounds
  67169. group
  67170. metals
  67171. review
  67172. verboom
  67173. reinhoudt
  67174. membered
  67175. cyclic
  67176. nitron
  67177. review
  67178. verboom
  67179. reinhoudt
  67180. amino
  67181. effect
  67182. hetero
  67183. review
  67184. vereshechagin
  67185. conformations
  67186. membered
  67187. review
  67188. vernin
  67189. chemistry
  67190. heterocyclic
  67191. compounds
  67192. review
  67193. verpoorte
  67194. schripsema
  67195. cinchona
  67196. review
  67197. disulfoxides
  67198. sulfenyl
  67199. sulfinates
  67200. review
  67201. viehe
  67202. heinz
  67203. merenyi
  67204. robert
  67205. janousek
  67206. zdenek
  67207. captod
  67208. review
  67209. vinnik
  67210. obraztsov
  67211. mechanism
  67212. dehyd
  67213. review
  67214. chemistry
  67215. perfumes
  67216. based
  67217. labdane
  67218. review
  67219. vliegenihari
  67220. dorland
  67221. halbeek
  67222. review
  67223. chemical
  67224. analysis
  67225. polycyclic
  67226. review
  67227. vogel
  67228. emanuel
  67229. novel
  67230. porphyrinoids
  67231. review
  67232. vogel
  67233. pierre
  67234. hericenes
  67235. related
  67236. exocyclic
  67237. review
  67238. vol'pin
  67239. akhrem
  67240. orlinkov
  67241. aprotic
  67242. organic
  67243. review
  67244. vollhardt
  67245. cobalt
  67246. mediated
  67247. cycloaddition
  67248. review
  67249. volodarskii
  67250. advances
  67251. chemistry
  67252. stable
  67253. review
  67254. vorbrueggen
  67255. helmut
  67256. manfred
  67257. carbon
  67258. substitution
  67259. review
  67260. vorbruggen
  67261. helmut
  67262. advances
  67263. amination
  67264. nitrogen
  67265. review
  67266. voronkov
  67267. knutov
  67268. advances
  67269. chemistry
  67270. review
  67271. voronkov
  67272. mikhail
  67273. deryagina
  67274. eleonora
  67275. thermal
  67276. review
  67277. vurov
  67278. smirnova
  67279. protection
  67280. amino
  67281. review
  67282. carruthers
  67283. pergamon
  67284. press
  67285. organic
  67286. chemistry
  67287. review
  67288. ilsley
  67289. organomet
  67290. mercury
  67291. review
  67292. oppolzer
  67293. tetrahedron
  67294. tetrahedron
  67295. review
  67296. neumann
  67297. synthesis
  67298. butyltin
  67299. hydri
  67300. review
  67301. wachter
  67302. joachim
  67303. synthesis
  67304. structure
  67305. reactivity
  67306. review
  67307. wagner
  67308. conformational
  67309. flexibility
  67310. photochem
  67311. review
  67312. wagner
  67313. peter
  67314. biradicals
  67315. membered
  67316. review
  67317. wakefield
  67318. organolithium
  67319. methods
  67320. academic
  67321. press
  67322. review
  67323. walborsky
  67324. mechanism
  67325. grignard
  67326. reagent
  67327. formati
  67328. review
  67329. wallace
  67330. hydroxylamine
  67331. sulphonic
  67332. review
  67333. walling
  67334. innocent
  67335. bystander
  67336. looks
  67337. review
  67338. walsh
  67339. suicide
  67340. substrates
  67341. mechanism
  67342. based
  67343. enzyme
  67344. review
  67345. joullie
  67346. muscarine
  67347. alkaloids
  67348. alkaloids
  67349. review
  67350. henry
  67351. chemistry
  67352. cyclo
  67353. review
  67354. total
  67355. synthesis
  67356. yeast
  67357. alanine
  67358. transfer
  67359. review
  67360. asymmetric
  67361. synthesis
  67362. lignans
  67363. review
  67364. nonenzymic
  67365. asymmetric
  67366. transformations
  67367. review
  67368. synthesis
  67369. lignans
  67370. neolignans
  67371. review
  67372. warner
  67373. philip
  67374. strained
  67375. bridgehead
  67376. double
  67377. bonds
  67378. review
  67379. warren
  67380. organic
  67381. synthesis
  67382. disconnection
  67383. approa
  67384. review
  67385. washburne
  67386. organosilicon
  67387. primer
  67388. silicon
  67389. review
  67390. wasserman
  67391. total
  67392. synthesis
  67393. macrocy
  67394. review
  67395. wataru
  67396. chemistry
  67397. allene
  67398. episulfides
  67399. review
  67400. watson
  67401. stereochemistry
  67402. reactivity
  67403. review
  67404. hydride
  67405. shifts
  67406. transfers
  67407. review
  67408. watthey
  67409. stanton
  67410. azepines
  67411. review
  67412. waxman
  67413. strominger
  67414. lactam
  67415. antibiotics
  67416. review
  67417. wayner
  67418. daniel
  67419. griller
  67420. david
  67421. radical
  67422. thermo
  67423. review
  67424. webber
  67425. wheller
  67426. antimicrobial
  67427. pharmacoki
  67428. review
  67429. weber
  67430. czugler
  67431. functional
  67432. group
  67433. assisted
  67434. clathra
  67435. review
  67436. weber
  67437. toner
  67438. goldberg
  67439. voegtle
  67440. laidler
  67441. review
  67442. weber
  67443. metal
  67444. complexes
  67445. sulfur
  67446. ylides
  67447. coordinati
  67448. review
  67449. weber
  67450. silicon
  67451. reagents
  67452. organic
  67453. synthesis
  67454. review
  67455. weidmann
  67456. seebach
  67457. organometallic
  67458. compounds
  67459. review
  67460. weill
  67461. raynal
  67462. little
  67463. story
  67464. great
  67465. syntheses
  67466. review
  67467. weinreb
  67468. staib
  67469. synthetic
  67470. aspects
  67471. diels
  67472. review
  67473. weinreb
  67474. steven
  67475. scola
  67476. imines
  67477. review
  67478. weisman
  67479. nuclear
  67480. magnetic
  67481. resonance
  67482. analysis
  67483. review
  67484. weiss
  67485. carbene
  67486. complexes
  67487. intermediates
  67488. catal
  67489. review
  67490. weiss
  67491. riehard
  67492. thermotropic
  67493. liquid
  67494. crystals
  67495. review
  67496. welch
  67497. eswarakrishnan
  67498. effect
  67499. fluorinati
  67500. review
  67501. welch
  67502. eswarakrishnan
  67503. seetha
  67504. fluorine
  67505. review
  67506. weltner
  67507. william
  67508. richard
  67509. carbon
  67510. molecul
  67511. review
  67512. wender
  67513. siggel
  67514. lorenz
  67515. arene
  67516. alken
  67517. review
  67518. wender
  67519. ternansky
  67520. robert
  67521. delong
  67522. mitch
  67523. singh
  67524. review
  67525. wendt
  67526. reactivity
  67527. primary
  67528. radical
  67529. review
  67530. wentrup
  67531. reactive
  67532. molecules
  67533. wiley
  67534. interscience
  67535. review
  67536. werner
  67537. helmut
  67538. complexes
  67539. carbon
  67540. monoxide
  67541. review
  67542. werner
  67543. helmut
  67544. erker
  67545. gerhard
  67546. organometallics
  67547. review
  67548. werstiuk
  67549. homoenolate
  67550. anions
  67551. homoenolate
  67552. review
  67553. organopolysilanes
  67554. silicon
  67555. compounds
  67556. review
  67557. organopolysilanes
  67558. silicon
  67559. compounds
  67560. review
  67561. westley
  67562. chemical
  67563. transformations
  67564. polyether
  67565. review
  67566. westmoreland
  67567. david
  67568. rhodes
  67569. gerald
  67570. analytical
  67571. review
  67572. westwood
  67573. nicholas
  67574. ultraviolet
  67575. photoelectron
  67576. review
  67577. wetzel
  67578. goeddel
  67579. synthesis
  67580. polypeptides
  67581. review
  67582. white
  67583. james
  67584. organic
  67585. synthesis
  67586. wiley
  67587. review
  67588. whitesell
  67589. whitesell
  67590. alkylation
  67591. ketones
  67592. review
  67593. whitesell
  67594. james
  67595. symmetry
  67596. asymmetric
  67597. induct
  67598. review
  67599. whitesides
  67600. enzymes
  67601. catalysts
  67602. review
  67603. whitten
  67604. russell
  67605. schmehl
  67606. photochemical
  67607. review
  67608. wiberg
  67609. inverted
  67610. geometries
  67611. carbon
  67612. 198417
  67613. review
  67614. wiberg
  67615. resonance
  67616. interactions
  67617. acyclic
  67618. system
  67619. review
  67620. wiberg
  67621. kenneth
  67622. small
  67623. propellanes
  67624. review
  67625. wiberg
  67626. silyl
  67627. germyl
  67628. stannyl
  67629. derivatives
  67630. review
  67631. wielstra
  67632. yysen
  67633. gambarotta
  67634. sandro
  67635. chiang
  67636. michael
  67637. review
  67638. wiersum
  67639. flash
  67640. vacuum
  67641. thermolysis
  67642. versatile
  67643. review
  67644. wiersum
  67645. preparative
  67646. flash
  67647. vacuum
  67648. thermolysis
  67649. review
  67650. hannes
  67651. modern
  67652. synthetic
  67653. routes
  67654. towards
  67655. importa
  67656. review
  67657. bruce
  67658. highly
  67659. stereoselective
  67660. syntheses
  67661. review
  67662. williams
  67663. effective
  67664. charge
  67665. leffer's
  67666. index
  67667. review
  67668. williams
  67669. andrew
  67670. concerted
  67671. mechanisms
  67672. group
  67673. review
  67674. williams
  67675. structural
  67676. studies
  67677. antibiotics
  67678. review
  67679. williams
  67680. organic
  67681. polymeric
  67682. polymeric
  67683. review
  67684. williams
  67685. nitrosation
  67686. mechanisms
  67687. 198319
  67688. review
  67689. williams
  67690. sprague
  67691. novel
  67692. radical
  67693. anions
  67694. review
  67695. williams
  67696. robert
  67697. synthesis
  67698. optically
  67699. active
  67700. review
  67701. wilman
  67702. derry
  67703. chemistry
  67704. antitumor
  67705. review
  67706. wilman
  67707. derry
  67708. chemistry
  67709. antitumor
  67710. review
  67711. wilson
  67712. structure
  67713. reactivity
  67714. halosulfo
  67715. review
  67716. radical
  67717. reactions
  67718. silanes
  67719. reactive
  67720. review
  67721. winter
  67722. unsaturated
  67723. dimetal
  67724. cyclopentadienyl
  67725. review
  67726. wiswesser
  67727. william
  67728. johann
  67729. josef
  67730. loschmidt
  67731. review
  67732. witczak
  67733. synthesis
  67734. preparative
  67735. applications
  67736. review
  67737. witczak
  67738. whistler
  67739. carbohydrates
  67740. containing
  67741. review
  67742. withers
  67743. dinoflagellate
  67744. sterols
  67745. marine
  67746. natural
  67747. review
  67748. witkop
  67749. cossinger
  67750. amphibian
  67751. alkaloids
  67752. alkalo
  67753. review
  67754. witkop
  67755. forty
  67756. years
  67757. trypto
  67758. review
  67759. witkop
  67760. probing
  67761. channels
  67762. natural
  67763. review
  67764. enzymes
  67765. organic
  67766. synthesis
  67767. review
  67768. enzymic
  67769. catalysts
  67770. organic
  67771. synthesis
  67772. review
  67773. heterocycles
  67774. stereospecific
  67775. review
  67776. arene
  67777. syntheses
  67778. extru
  67779. review
  67780. arene
  67781. syntheses
  67782. review
  67783. henry
  67784. review
  67785. henry
  67786. synthesis
  67787. novel
  67788. benzenoid
  67789. molecul
  67790. review
  67791. recent
  67792. application
  67793. field
  67794. ionizatio
  67795. review
  67796. wozniak
  67797. chojnowski
  67798. silyl
  67799. esters
  67800. phosphorus
  67801. review
  67802. wozniak
  67803. advances
  67804. chemistr
  67805. review
  67806. wrackmeyer
  67807. bernd
  67808. multinuclear
  67809. chemistry
  67810. review
  67811. wubbels
  67812. catalysis
  67813. photochemical
  67814. reactions
  67815. review
  67816. organic
  67817. metals
  67818. superconductors
  67819. manag
  67820. review
  67821. wulff
  67822. william
  67823. transition
  67824. metal
  67825. carbene
  67826. complexes
  67827. review
  67828. wynberg
  67829. meijer
  67830. reimer
  67831. tiemann
  67832. reaction
  67833. review
  67834. review
  67835. matsuda
  67836. goton
  67837. heterocycles
  67838. review
  67839. okamoto
  67840. takagi
  67841. heterocycl
  67842. review
  67843. tamaru
  67844. yoshida
  67845. orqanomet
  67846. heteroc
  67847. review
  67848. yamamoto
  67849. acyclic
  67850. stereoc
  67851. review
  67852. yamamoto
  67853. aldrichimica
  67854. allylic
  67855. review
  67856. yablokova
  67857. aleksandrov
  67858. catalytic
  67859. decomposit
  67860. review
  67861. yadav
  67862. desbpande
  67863. prassd
  67864. sharma
  67865. synthesis
  67866. review
  67867. yagupol'skii
  67868. il'chenko
  67869. gandel'sman
  67870. review
  67871. yajima
  67872. jujii
  67873. acidolytic
  67874. deprotection
  67875. procedures
  67876. review
  67877. yakhontov
  67878. krasnokutskaya
  67879. advances
  67880. review
  67881. yakobson
  67882. akhmetova
  67883. alkali
  67884. metal
  67885. fluorides
  67886. review
  67887. yamaguchi
  67888. masao
  67889. miyazawa
  67890. takeo
  67891. takata
  67892. toshikazu
  67893. review
  67894. yamaguchi
  67895. nuclear
  67896. magnetic
  67897. resonance
  67898. analysis
  67899. review
  67900. yamamoto
  67901. inokawa
  67902. sugar
  67903. analogs
  67904. having
  67905. phosphoru
  67906. review
  67907. yamamoto
  67908. hisashi
  67909. maruoka
  67910. keiji
  67911. furuta
  67912. kyoji
  67913. naruse
  67914. review
  67915. yamamoto
  67916. hisashi
  67917. maruoka
  67918. keiji
  67919. organoaluminum
  67920. reage
  67921. review
  67922. yamamoto
  67923. maruyama
  67924. organometallic
  67925. compounds
  67926. review
  67927. yamanaka
  67928. hiroshi
  67929. sakamoto
  67930. takao
  67931. niitsuma
  67932. setsuko
  67933. review
  67934. yashin
  67935. chromatographic
  67936. retention
  67937. parameters
  67938. review
  67939. yasuda
  67940. masahide
  67941. shima
  67942. kensuke
  67943. amination
  67944. electron
  67945. review
  67946. yicens
  67947. bohmer
  67948. calixarenes
  67949. versatile
  67950. class
  67951. review
  67952. yokoyama
  67953. imamoto
  67954. organic
  67955. reactions
  67956. carbon
  67957. review
  67958. yokoyama
  67959. masahka
  67960. watanabe
  67961. satoshi
  67962. sujino
  67963. keiko
  67964. review
  67965. yokoyama
  67966. masataka
  67967. hideo
  67968. kondo
  67969. shinichi
  67970. synthes
  67971. review
  67972. yokoyama
  67973. masataka
  67974. hideo
  67975. synthesis
  67976. heterocyc
  67977. review
  67978. yoshida
  67979. electrooxidation
  67980. organic
  67981. chemistry
  67982. review
  67983. yoshida
  67984. shiba
  67985. ohshiro
  67986. aspects
  67987. review
  67988. yoshimura
  67989. synthesis
  67990. branched
  67991. chain
  67992. sugars
  67993. review
  67994. yoshioka
  67995. parvez
  67996. miyazaki
  67997. parvez
  67998. supercr
  67999. review
  68000. gololobov
  68001. tetrahedron
  68002. twent
  68003. review
  68004. todres
  68005. tetrahedron
  68006. tetrahedron
  68007. review
  68008. zabolotskii
  68009. myagkova
  68010. evstigneeva
  68011. inhibi
  68012. review
  68013. zakrewski
  68014. janusz
  68015. reactions
  68016. pyrrolyl
  68017. review
  68018. yashin
  68019. chromatographic
  68020. retention
  68021. parameters
  68022. review
  68023. zamir
  68024. lolita
  68025. biosynthesis
  68026. acetyldeoxynivalen@
  68027. review
  68028. liming
  68029. tedford
  68030. catriona
  68031. applications
  68032. perlin
  68033. problems
  68034. stereochemistry
  68035. carbon@
  68036. simple
  68037. method
  68038. chelation
  68039. controlled
  68040. additions
  68041. amin@
  68042. stereoselective
  68043. synthesis
  68044. isoiridomyrmecin
  68045. application
  68046. study
  68047. rhodium-vinylallene
  68048. complexes
  68049. leading
  68050. application
  68051. mechanistic
  68052. model
  68053. leads
  68054. extens@
  68055. total
  68056. synthesis
  68057. gelsimine@
  68058. unified
  68059. mechanistic
  68060. oxidative
  68061. reactions
  68062. catalyzed
  68063. versatile
  68064. asymmetric
  68065. synthesis
  68066. b-branched
  68067. a-amino
  68068. acids@
  68069. a-alkyl-b-ketophosph@
  68070. a-amino
  68071. a-chloro-b-lactones@
  68072. abeles
  68073. robert
  68074. methionine
  68075. salvage
  68076. pathway
  68077. 199225
  68078. abstract@
  68079. academic
  68080. account@
  68081. accounts
  68082. accumulation
  68083. acetates@
  68084. acetogenins@
  68085. review
  68086. zamir
  68087. lolita
  68088. biosynthesis
  68089. acetyldeoxynivalen
  68090. review
  68091. zamoiski
  68092. banaszek
  68093. grynkiewicz
  68094. synthesis
  68095. review
  68096. zander
  68097. maximilian
  68098. molecular
  68099. topology
  68100. chemical
  68101. review
  68102. zaugg
  68103. amidoalkylation
  68104. carbon
  68105. recent
  68106. advanc
  68107. review
  68108. zdanovich
  68109. seitembetova
  68110. setkina
  68111. transit
  68112. review
  68113. zefirov
  68114. makhon'kov
  68115. philic
  68116. reactions
  68117. review
  68118. zefirov
  68119. zhdankin
  68120. koz'min
  68121. synthesis
  68122. review
  68123. zefirov
  68124. nikolai
  68125. palyulin
  68126. vladmmir
  68127. conformational
  68128. review
  68129. zehavi
  68130. applications
  68131. photosensitive
  68132. protectin
  68133. review
  68134. zeifman
  68135. gabrielyan
  68136. gamibaryan
  68137. review
  68138. zelewski
  68139. romuald
  68140. application
  68141. principal
  68142. compone
  68143. review
  68144. zenneck
  68145. ulrich
  68146. reactive
  68147. complexes
  68148. electron
  68149. review
  68150. zhang
  68151. xiaofeng
  68152. rongsi
  68153. existence
  68154. review
  68155. weishan
  68156. synthesis
  68157. brassinosteroid
  68158. review
  68159. liming
  68160. tedford
  68161. catriona
  68162. applications
  68163. review
  68164. liming
  68165. tedford
  68166. catriona
  68167. applications
  68168. review
  68169. zimmerman
  68170. theoretical
  68171. aspects
  68172. organic
  68173. review
  68174. zimmerman
  68175. topics
  68176. photochemistry
  68177. review
  68178. zlotin
  68179. varnaeva
  68180. luk'yanova
  68181. nitronitri
  68182. review
  68183. zoellner
  68184. klabunde
  68185. alkynes
  68186. metal
  68187. atoms
  68188. review
  68189. zoller
  68190. three
  68191. membered
  68192. rings
  68193. containing
  68194. sulfur
  68195. review
  68196. zorkii
  68197. masunov
  68198. diffractometric
  68199. invest
  68200. review
  68201. nefedov
  68202. spectroscopic
  68203. study
  68204. carbene
  68205. review
  68206. zvezdina
  68207. zhadonva
  68208. dorofeenko
  68209. reactions
  68210. review
  68211. zwanenburg
  68212. chemistry
  68213. sulfines
  68214. review
  68215. zwanenburg
  68216. binne
  68217. sulfine
  68218. chemistry
  68219. reviews
  68220. heter
  68221. review
  68222. zweifel
  68223. miller
  68224. synthesis
  68225. using
  68226. alkyne
  68227. derived
  68228. temperature
  68229. preparation
  68230. alkenyllithiums
  68231. lithium
  68232. route
  68233. fused
  68234. heterocycles
  68235. involving
  68236. amine
  68237. addition
  68238. ryabov
  68239. synthesis
  68240. cyclopalladated
  68241. complexes
  68242. perlin
  68243. problems
  68244. stereochemistry
  68245. carbon
  68246. replicating
  68247. system
  68248. experimental
  68249. short
  68250. route
  68251. avenaciolide
  68252. isoavenaciolide
  68253. radica
  68254. short
  68255. stereocontrolled
  68256. synthesis
  68257. hydroxyethylene
  68258. dipept
  68259. short
  68260. stereocontrolled
  68261. synthesis
  68262. strychnine
  68263. short
  68264. stereoselective
  68265. synthesis
  68266. trans
  68267. hydroxy
  68268. short
  68269. synthesis
  68270. target
  68271. tandem
  68272. intramolecular
  68273. short
  68274. synthesis
  68275. lycoricidine
  68276. simple
  68277. efficient
  68278. preparation
  68279. methoxymethyl
  68280. esters
  68281. simple
  68282. efficient
  68283. procedure
  68284. preparation
  68285. simple
  68286. efficient
  68287. substituted
  68288. halogenopyruvami
  68289. simple
  68290. highly
  68291. diastereoselective
  68292. synthesis
  68293. simple
  68294. asymmetric
  68295. synthesis
  68296. substituted
  68297. dihydro
  68298. simple
  68299. catalytic
  68300. method
  68301. conversion
  68302. bromide
  68303. simple
  68304. efficient
  68305. preparation
  68306. trimethylsiloxy
  68307. simple
  68308. method
  68309. chelation
  68310. controlled
  68311. additions
  68312. simple
  68313. method
  68314. preparation
  68315. oxindolacetic
  68316. simple
  68317. method
  68318. synthesis
  68319. carbamates
  68320. simple
  68321. method
  68322. prepare
  68323. unsymmetrical
  68324. tetrasul
  68325. simple
  68326. procedure
  68327. synthesis
  68328. oxadiazo
  68329. simple
  68330. synthesis
  68331. tricarbonyl
  68332. compounds
  68333. diketo
  68334. simple
  68335. synthesis
  68336. difluorocyclopropane
  68337. bromofor
  68338. simple
  68339. synthesis
  68340. heterocycles
  68341. diphenylsulfilimi
  68342. simple
  68343. versatile
  68344. synthetic
  68345. route
  68346. heteroaryl
  68347. single
  68348. synthesis
  68349. trisubstituted
  68350. dihydronapht
  68351. synthesis
  68352. camptothecin
  68353. using
  68354. palladium
  68355. chemist
  68356. stereocontrolled
  68357. organopalladium
  68358. route
  68359. disubstituted
  68360. stereoselective
  68361. approach
  68362. annulated
  68363. tetrahydrofurans
  68364. stereoselective
  68365. organopalladium
  68366. route
  68367. toward
  68368. perhydrohistr
  68369. stereoselective
  68370. synthesis
  68371. methylcarbapenem
  68372. stereoselective
  68373. synthesis
  68374. isoiridomyrmecin
  68375. application
  68376. stereospecific
  68377. synthesis
  68378. disubstituted
  68379. tetrahydrofur
  68380. straightforward
  68381. practical
  68382. formal
  68383. synthesis
  68384. lavendam
  68385. straightforward
  68386. preparation
  68387. indoles
  68388. intram
  68389. study
  68390. hetero
  68391. diels
  68392. alder
  68393. reaction
  68394. alkyl
  68395. study
  68396. intramolecular
  68397. stille
  68398. cross
  68399. coupling
  68400. reaction
  68401. study
  68402. reaction
  68403. calicheamicin
  68404. glutathione
  68405. study
  68406. regioselectivity
  68407. radical
  68408. addition
  68409. substrate
  68410. model
  68411. enzymic
  68412. resolution
  68413. esters
  68414. sugar
  68415. based
  68416. designer
  68417. against
  68418. influenza
  68419. sulfur
  68420. stabilized
  68421. surprising
  68422. observation
  68423. about
  68424. mitsunobu
  68425. reactions
  68426. solid
  68427. survey
  68428. methods
  68429. preparation
  68430. pyrrolopyrimidine
  68431. survey
  68432. natural
  68433. products
  68434. which
  68435. abstract
  68436. hydrogen
  68437. atoms
  68438. survey
  68439. novel
  68440. useful
  68441. reactions
  68442. discovered
  68443. through
  68444. survey
  68445. radical
  68446. mediated
  68447. cyclization
  68448. acetals
  68449. survey
  68450. strained
  68451. organic
  68452. molecules
  68453. survey
  68454. radical-mediated
  68455. cyclization
  68456. alpha-halo
  68457. suzuki
  68458. lecture
  68459. applications
  68460. synthesis
  68461. luffariolide
  68462. 12-metallate
  68463. rearran
  68464. synthesis
  68465. pyrrolophenanthridon
  68466. alkaloids
  68467. consecutiv
  68468. synthesis
  68469. supinidine
  68470. intramolecular
  68471. carbenoid
  68472. synthesis
  68473. spiroketal
  68474. subunit
  68475. calyculin
  68476. tallec
  68477. asymmetric
  68478. synthesis
  68479. tandem
  68480. cycloaddition
  68481. protocol
  68482. controlled
  68483. synthesis
  68484. tandem
  68485. oxy-cope
  68486. transannular
  68487. closure
  68488. route
  68489. polyqui
  68490. taurins
  68491. chemistry
  68492. cyclazines
  68493. special
  68494. topics
  68495. tellurium
  68496. transposition
  68497. route
  68498. allylic
  68499. alcohols
  68500. overcomi
  68501. stroll
  68502. chemistry
  68503. nickel-containing
  68504. total
  68505. synthesis
  68506. gelsemine
  68507. oxindole
  68508. spiroannelation
  68509. total
  68510. synthesis
  68511. gelsimine
  68512. total
  68513. synthesis
  68514. sativene
  68515. pressure
  68516. diels
  68517. alder
  68518. total
  68519. synthesis
  68520. taxol
  68521. total
  68522. synthesis
  68523. xestospongin
  68524. araguspongine
  68525. three
  68526. component
  68527. synthesis
  68528. utilization
  68529. unified
  68530. entry
  68531. ingenane
  68532. tigliane
  68533. taxane
  68534. strategy
  68535. synthesis
  68536. highly
  68537. substituted
  68538. unified
  68539. ketone
  68540. photochemistry
  68541. useful
  68542. enantiomerically
  68543. synthon
  68544. malic
  68545. useful
  68546. preparation
  68547. pyrroles
  68548. unsaturated
  68549. sulfon
  68550. el'tsov
  68551. studzinskii
  68552. grebenkina
  68553. photoinitiati
  68554. eremeev
  68555. el'kinsonm
  68556. heterocyclic
  68557. compds
  68558. folkin
  68559. kolomiets
  68560. ivashchenko
  68561. dziomko
  68562. reactions
  68563. isatins
  68564. kamernitzky
  68565. turuta
  68566. synthesis
  68567. steroidal
  68568. hetero
  68569. versatile
  68570. approach
  68571. cyclic
  68572. ethers
  68573. synthesis
  68574. disubstit
  68575. versatile
  68576. asymmetric
  68577. synthesis
  68578. b-branched
  68579. a-amino
  68580. acids
  68581. versatile
  68582. one-pot
  68583. procedure
  68584. insertion
  68585. 3-subst
  68586. versatile
  68587. radical
  68588. based
  68589. synthesis
  68590. lactams
  68591. using
  68592. nicke
  68593. versatile
  68594. radical
  68595. based
  68596. synthesis
  68597. g-lactams
  68598. using
  68599. nicke
  68600. versatile
  68601. synthesis
  68602. butenolides
  68603. unsaturated
  68604. esters
  68605. vinylzirconation
  68606. reaction
  68607. alkynes
  68608. johnson
  68609. porphyrins
  68610. related
  68611. williams
  68612. douglas
  68613. group
  68614. transfer
  68615. elimination
  68616. yamamoto
  68617. organomet
  68618. transition
  68619. metal
  68620. yoshikoshi
  68621. miyashita
  68622. oxoalky
  68623. zlatkis
  68624. kaiser
  68625. hptlc
  68626. performance
  68627. layer
  68628. a'-lithiation
  68629. a-acetamidoacrylates
  68630. a-alkenyl
  68631. a-alkoxy
  68632. a-alkoxy-b-methyl
  68633. a-alkoxystannane
  68634. lkylation
  68635. stereochemistry
  68636. trans
  68637. decahyd
  68638. a-allenic
  68639. a-allylation
  68640. a-amido
  68641. a-amino
  68642. a-amino
  68643. a-aminoorganolithium
  68644. a-aminostannanes
  68645. a-aryl
  68646. a-azidonation
  68647. a-azidonation
  68648. amides
  68649. carbamates
  68650. ureas
  68651. iodosy
  68652. a-chloro
  68653. a-cyano
  68654. a-dialkyl
  68655. a-dictyopterol
  68656. a-fused
  68657. a-glucosides
  68658. a-heteroatom-substit
  68659. a-hydroxy
  68660. a-hydroxyallylation
  68661. a-hydroxyallylborati
  68662. a-iodoenones
  68663. a-keto
  68664. a-ketosulfonium
  68665. a-lithio-g-methoxyal
  68666. a-lithioamine
  68667. a-lycorane
  68668. a-nitro
  68669. a-otbs
  68670. a-oxo
  68671. a-oxoketene
  68672. a-oxoketene
  68673. n-acetals
  68674. versatile
  68675. intermediates
  68676. a-ring
  68677. a-substituted
  68678. a-sulfinyl
  68679. a-sulfinylcyclopente
  68680. a-trimethylsilyl
  68681. a-virus
  68682. a58365a
  68683. aakeroy
  68684. aakeroy
  68685. christer
  68686. seddon
  68687. kenneth
  68688. hydrogen
  68689. aaron
  68690. aaron
  68691. conformational
  68692. analysis
  68693. intramolecular
  68694. hydrogen
  68695. aasen
  68696. antonio
  68697. agullo
  68698. consuelo
  68699. manuel
  68700. domingo
  68701. abalonin
  68702. abalonin
  68703. investigations
  68704. arbuzov
  68705. retro
  68706. arbuzov
  68707. abboud
  68708. abboud
  68709. kamlet
  68710. examination
  68711. linear
  68712. abboud
  68713. notario
  68714. rafael
  68715. bertran
  68716. miquel
  68717. abdalla
  68718. abdel
  68719. abdou
  68720. abdoust
  68721. abdreimova
  68722. abdulganeva
  68723. abdulganeva
  68724. erzhanov
  68725. acetylenic
  68726. amino
  68727. acids
  68728. russian
  68729. abdulla
  68730. abdulla
  68731. brinkmeyer
  68732. chemistry
  68733. formamide
  68734. acetal
  68735. ikuro
  68736. rohmer
  68737. michel
  68738. prestwich
  68739. glenn
  68740. enzymatic
  68741. cyclizat
  68742. abegas
  68743. mucklejohn
  68744. chemistry
  68745. phosphinimines
  68746. abeles
  68747. abeles
  68748. robert
  68749. methionine
  68750. salvage
  68751. pathway
  68752. 199225
  68753. abell
  68754. abell
  68755. anders
  68756. latent
  68757. reactivity
  68758. study
  68759. enzyme
  68760. mechani
  68761. abelman
  68762. aberhart
  68763. ability
  68764. abnormal
  68765. gharbia
  68766. joullie
  68767. reactions
  68768. nitrones
  68769. about
  68770. enkov
  68771. abramova
  68772. abramovitch
  68773. abramovitch
  68774. rudolph
  68775. applications
  68776. microwave
  68777. energy
  68778. abronin
  68779. abronin
  68780. balen
  68781. gol'dfarb
  68782. electrophilic
  68783. subst
  68784. absence
  68785. absolute
  68786. absolute
  68787. asymmetric
  68788. synthesis
  68789. irradiation
  68790. chiral
  68791. cryst
  68792. absolute
  68793. kinetics
  68794. intramolecular
  68795. alklycarbene
  68796. reactions
  68797. absorption
  68798. abstr
  68799. abstract
  68800. abstraction
  68801. abundance
  68802. abundant
  68803. academicP
  68804. academic
  68805. academic
  68806. accelerated
  68807. acceleration
  68808. acceleration
  68809. selectivity
  68810. enhancement
  68811. diels-alder
  68812. acceptor
  68813. acceptors
  68814. access
  68815. accessible
  68816. accompanied
  68817. accompanying
  68818. accountn
  68819. accounts
  68820. accounts
  68821. accts
  68822. accumulation
  68823. accumulation
  68824. acepleiadienes
  68825. acerosolide
  68826. acetal
  68827. acetal
  68828. template
  68829. synthesis
  68830. trans-25-disubstitut
  68831. acetal-vinyl
  68832. acetalization
  68833. acetals
  68834. acetamide
  68835. acetamido
  68836. acetanilide
  68837. acetate
  68838. acetic
  68839. anhydride
  68840. acetic
  68841. formic
  68842. anhydride
  68843. acetic
  68844. formic
  68845. anhydride
  68846. review
  68847. aceto
  68848. acetoacetamide
  68849. acetoacetanilide
  68850. acetoacetate
  68851. acetoacetic
  68852. acetogenins
  68853. acetolysis
  68854. acetonation
  68855. acetonide
  68856. acetonides
  68857. acetonitrile
  68858. acetonitriles
  68859. acetophenone
  68860. acetophenones
  68861. acetoxy
  68862. acetoxycrenulide
  68863. acetoxycyclohexenes
  68864. acetoxylation
  68865. acetyl
  68866. cetone
  68867. acetylation
  68868. acetylation
  68869. diketone
  68870. copper
  68871. chelates
  68872. treatment
  68873. acetylcyclopropane
  68874. acetyldeoxynivalenol
  68875. acetylene
  68876. acetylene
  68877. diethers
  68878. logical
  68879. entry
  68880. oxocarbons
  68881. acetylene
  68882. equivalents
  68883. cycloaddition
  68884. processes
  68885. acetylene
  68886. equivalents
  68887. cycloaddition
  68888. reactions
  68889. acetylene-methylenec
  68890. acetylenecarboxylic
  68891. acetylenedicarboxyla
  68892. acetylenes
  68893. acetylenes
  68894. acetylenes
  68895. synthesis
  68896. acetylenes-selective
  68897. acetylenic
  68898. acetylenic
  68899. amino
  68900. acids
  68901. acetylenic
  68902. ethers
  68903. their
  68904. analogues
  68905. acetylenic
  68906. sulfinates
  68907. organic
  68908. synthesis
  68909. diels
  68910. alder
  68911. react
  68912. acetylide
  68913. acetylides
  68914. acetylindole
  68915. acetylneuraminic
  68916. acetylsydnones
  68917. acher
  68918. acher
  68919. neurophysins
  68920. molecular
  68921. cellular
  68922. aspects
  68923. acheson
  68924. acheson
  68925. elmore
  68926. reactions
  68927. acetylenecarboxylic
  68928. acheson
  68929. chemistry
  68930. reactions
  68931. properties
  68932. achieve
  68933. achim
  68934. achiral
  68935. achiwa
  68936. achyutha
  68937. achyutha
  68938. acidz
  68939. reactions
  68940. acylamino
  68941. lactams
  68942. observati
  68943. properties
  68944. electronically
  68945. excited
  68946. states
  68947. catalyzed
  68948. pyrone
  68949. formation
  68950. reactions
  68951. catalyzed
  68952. intramolecular
  68953. diels
  68954. alder
  68955. reactions
  68956. lithi
  68957. catalyzed
  68958. ionic
  68959. diels-alder
  68960. reactions
  68961. concentrated
  68962. induced
  68963. stereoselective
  68964. formation
  68965. cycloheptadien
  68966. promoted
  68967. decomposition
  68968. diazo
  68969. ketones
  68970. acid-18
  68971. acid-base
  68972. acid-base
  68973. dissociation
  68974. constants
  68975. dipolar
  68976. aprotic
  68977. solvents
  68978. acid-catalyzed
  68979. acid-catalyzed
  68980. rearrangement
  68981. epoxides
  68982. acid-cryptand
  68983. acid-enhanced
  68984. acid-promoted
  68985. acides
  68986. acidic
  68987. acidic
  68988. basic
  68989. hydrolysis
  68990. amides
  68991. acidities
  68992. acidity
  68993. acidolytic
  68994. acidsr
  68995. acids
  68996. acids
  68997. ackroyd
  68998. aconite
  68999. aconitum
  69000. acridine
  69001. acridines
  69002. acridines
  69003. dibenzo
  69004. pyridines
  69005. acridinium
  69006. acridizinium
  69007. acridone
  69008. acrolein
  69009. acronycine
  69010. across
  69011. acrylaldehydes
  69012. acrylamide
  69013. acrylate
  69014. acrylic
  69015. acrylonitrile
  69016. acrylonitriles
  69017. scand
  69018. synthetic
  69019. studies
  69020. optically
  69021. acting
  69022. actinide
  69023. actinides
  69024. actinomycetes
  69025. action
  69026. actions
  69027. activa
  69028. activat
  69029. activate
  69030. activatedE
  69031. activated
  69032. activated
  69033. cyclopropanes
  69034. synthesis
  69035. membered
  69036. activated
  69037. cyclopropanes
  69038. synthesis
  69039. five-membered
  69040. activated
  69041. dimethyl
  69042. sulfoxide
  69043. useful
  69044. reagents
  69045. synthesis
  69046. activated
  69047. metals
  69048. organic
  69049. synthesis
  69050. activatedc
  69051. activating
  69052. activation
  69053. activation
  69054. functionalization
  69055. alkanes
  69056. activation
  69057. protection
  69058. carboxyl
  69059. group
  69060. activation
  69061. alkynes
  69062. ruthenium
  69063. complexes
  69064. activation
  69065. carbon
  69066. fluorine
  69067. bonds
  69068. metal
  69069. complexes
  69070. activation
  69071. carbon-fluorine
  69072. bonds
  69073. metal
  69074. complexes
  69075. activation
  69076. grignard
  69077. reagents
  69078. transition
  69079. metal
  69080. compound
  69081. activation
  69082. hydrogen
  69083. peroxide
  69084. organic
  69085. compounds
  69086. activation
  69087. superoxide
  69088. application
  69089. peroxysulfur
  69090. interme
  69091. activation
  69092. superoxide
  69093. organic
  69094. synthesis
  69095. using
  69096. peroxysulfu
  69097. activation
  69098. carbon-hydrogen
  69099. metal
  69100. complexes
  69101. activations
  69102. activators
  69103. activet
  69104. activation
  69105. alkynes
  69106. ruthenium
  69107. complexes@
  69108. active
  69109. activitg@
  69110. acyclic
  69111. acyclic
  69112. butadiene-iron
  69113. tricarbonyl
  69114. complexes
  69115. organic
  69116. synt@
  69117. acyclic
  69118. stereocontrol
  69119. radical
  69120. reactions
  69121. p-selectivity
  69122. organochromium
  69123. compounds
  69124. aldehydes
  69125. nozaki@
  69126. addition
  69127. reduction
  69128. oxidation
  69129. reactions
  69130. nitrosobenzene@
  69131. additive
  69132. solvent
  69133. effects
  69134. reductions
  69135. effects
  69136. advance@
  69137. advances
  69138. advances
  69139. stereochemical
  69140. control
  69141. 13-diol
  69142. system@
  69143. afarinkia
  69144. kamyar
  69145. vinader
  69146. victoria
  69147. nelson
  69148. posner
  69149. agents
  69150. ahuja@
  69151. akiba
  69152. inamoto
  69153. chemistry
  69154. nitrosoimines
  69155. 1131@
  69156. albrecht
  69157. alcohols
  69158. aldehydes
  69159. alder
  69160. aldrichimica@
  69161. alexander
  69162. alkadienyl@
  69163. alkaloids
  69164. alkene
  69165. metathesis
  69166. related
  69167. reactions@
  69168. alkenolides@
  69169. alkoxypropenes@
  69170. alkylamines@
  69171. active
  69172. activityU
  69173. actual~
  69174. acyclic
  69175. acyclic
  69176. acyclic
  69177. 14-diastereoselectiv
  69178. g-substituted
  69179. a-enones
  69180. trans
  69181. selection
  69182. intermolecular
  69183. racical
  69184. acyclic
  69185. diastereofacial
  69186. selection
  69187. intermolecular
  69188. radical
  69189. acyclic
  69190. dithiocarboxylic
  69191. esters-reactions
  69192. syntheses
  69193. acyclic
  69194. oxy-cope
  69195. rearrangement
  69196. dependence
  69197. stereoselec
  69198. acyclic
  69199. stereochemical
  69200. control
  69201. free-radical
  69202. reactions
  69203. acyclic
  69204. stereocontrol
  69205. fischer
  69206. carbene
  69207. chemistry
  69208. acyclic
  69209. stereocontrol
  69210. michael
  69211. addition
  69212. reactions
  69213. enami
  69214. acyclic
  69215. stereocontrol
  69216. wittig
  69217. sigmatropic
  69218. rearrangemen
  69219. acyclic
  69220. stereocontrol
  69221. allylic
  69222. organometallic
  69223. compounds
  69224. acyclonucleosides
  69225. alkyl
  69226. peroxides
  69227. alpha-heterosubstitu
  69228. alkyl
  69229. peroxides
  69230. anions
  69231. their
  69232. derivatives
  69233. nitroxides
  69234. reactions
  69235. reactivity
  69236. organotellurium
  69237. te-organotellurocarb
  69238. acyl-coa
  69239. acylaminocinnamates
  69240. acylaminoindazoles
  69241. acylarylnitrosamines
  69242. acylated
  69243. acylating
  69244. acylation
  69245. acylation
  69246. esters
  69247. ketones
  69248. nitriles
  69249. acylations
  69250. acylbenzimidazoles
  69251. acylcarbenium
  69252. acylcyanation
  69253. acylcyanation
  69254. terminal
  69255. acetylenes
  69256. palladium
  69257. catalyzed
  69258. acyldihydroquinoline
  69259. acylethenyl
  69260. acylhydrazones
  69261. acylic
  69262. acylimidazoles
  69263. acylimines
  69264. acyliminium
  69265. acyliminium
  69266. acyliminium
  69267. derived
  69268. rearrangement
  69269. bischler
  69270. acylindole
  69271. acylindoles
  69272. acyliron
  69273. acylium
  69274. acylketene
  69275. acylmethyl
  69276. acylnitrenium
  69277. acylnitroso
  69278. acyloin
  69279. acyloin
  69280. coupling
  69281. reactions
  69282. acyloin
  69283. rearrangement
  69284. hydroxy
  69285. acetals
  69286. application
  69287. acyloins
  69288. acyloxy
  69289. acyloxyalkyl
  69290. acyloxyborohydrides
  69291. acyloxylation
  69292. acylphenylacetates
  69293. acylphosphonates
  69294. acylpyrazines
  69295. acylpyrazoles
  69296. acylpyridines
  69297. acylpyrimidines
  69298. acylrhodium
  69299. acylsilane
  69300. acylsilanes
  69301. acyltetramic
  69302. acylthiohydroxamates
  69303. acylvinyl
  69304. adalbert
  69305. balci
  69306. cyclic
  69307. polyepoxides
  69308. synthetic
  69309. structural
  69310. lucchi
  69311. synthesis
  69312. unusual
  69313. organic
  69314. molecule
  69315. oxygen
  69316. diradicals
  69317. derived
  69318. cyclic
  69319. peroxides
  69320. 19791
  69321. waldemar
  69322. hadjiarapoglou
  69323. lazaros
  69324. dioxiranes
  69325. oxidation
  69326. waldemar
  69327. richter
  69328. markus
  69329. metal
  69330. catalyzed
  69331. direct
  69332. hydrox
  69333. adamantane
  69334. adamantanes
  69335. adamantanones
  69336. adams
  69337. adams
  69338. julian
  69339. spero
  69340. denice
  69341. rhodium
  69342. catalyzed
  69343. reactions
  69344. adams
  69345. insertion
  69346. alkynes
  69347. metal
  69348. metal
  69349. bonds
  69350. adant
  69351. adaptation
  69352. added
  69353. addends
  69354. addendum
  69355. addit
  69356. additionI
  69357. addition
  69358. addition
  69359. oaddition
  69360. reactions
  69361. photoinduced
  69362. electr
  69363. addition
  69364. substitution
  69365. reactions
  69366. nitrile
  69367. stabilized
  69368. addition
  69369. substitution
  69370. reactions
  69371. nitrile-stabilised
  69372. addition
  69373. carbenium
  69374. alkenes
  69375. addition
  69376. chiral
  69377. nucleophiles
  69378. aldehydes
  69379. ketones
  69380. addition
  69381. dilithiated
  69382. methyl
  69383. aminobutanoate
  69384. aldehydes
  69385. addition
  69386. reagents
  69387. alkenes
  69388. alkynes
  69389. addition
  69390. ketocarbenes
  69391. alkenes
  69392. alkynes
  69393. aromatic
  69394. addition
  69395. organochromium
  69396. compounds
  69397. aldehydes
  69398. nozaki
  69399. addition
  69400. organometallic
  69401. reagents
  69402. chiral
  69403. vinylic
  69404. sulfox
  69405. addition
  69406. stabilised
  69407. carbon
  69408. nucleophiles
  69409. n-alkylpyridin
  69410. addition
  69411. thiols
  69412. acetylene
  69413. substituted
  69414. indoles
  69415. addition
  69416. homoenolates
  69417. acetylenic
  69418. esters
  69419. amide
  69420. addition
  69421. reactions
  69422. butadiene
  69423. catalysed
  69424. palladium
  69425. compl
  69426. addition
  69427. reactions
  69428. esters
  69429. phosphorus
  69430. acids
  69431. addition
  69432. reactions
  69433. ketenes
  69434. addition
  69435. reactions
  69436. formation
  69437. carbon-halogen
  69438. bonds
  69439. addition
  69440. reactions
  69441. formation
  69442. carbon-nitrogen
  69443. bonds
  69444. addition
  69445. reactions
  69446. formation
  69447. carbon-oxygen
  69448. bonds
  69449. addition
  69450. reactions
  69451. formation
  69452. carbon-oxygen
  69453. bonds
  69454. addition
  69455. reactions
  69456. formation
  69457. carbon-oxygen
  69458. bonds
  69459. addition
  69460. reactions
  69461. formation
  69462. carbon-oxygen
  69463. bonds
  69464. addition
  69465. reactions
  69466. formation
  69467. carbon-sulfur
  69468. carbon
  69469. addition
  69470. reduction
  69471. oxidation
  69472. reactions
  69473. nitrosobenzene
  69474. addition-carbene
  69475. addition-electrophil
  69476. addition-elimination
  69477. addition-enolate
  69478. addition-ireland
  69479. addition-solvolysis
  69480. addition/cyclization
  69481. addition/trapping
  69482. additional
  69483. additionsI
  69484. additions
  69485. lithiated
  69486. hydroxy
  69487. alkyldiphenylphosphi
  69488. oxides
  69489. additions
  69490. n-acyliminium
  69491. additions
  69492. activated
  69493. triple
  69494. additive
  69495. additive
  69496. solvent
  69497. effects
  69498. reductions
  69499. effects
  69500. additive
  69501. solvent
  69502. effects
  69503. reductions
  69504. effects
  69505. additives
  69506. additivity
  69507. adduct
  69508. adducts
  69509. andersch
  69510. berger
  69511. goergens
  69512. seemayer
  69513. schneider
  69514. adiabatic
  69515. adiabatic
  69516. photoreactions
  69517. organic
  69518. molecules
  69519. adjacent
  69520. adjavcent
  69521. adjust
  69522. adkins
  69523. adlington
  69524. adolf
  69525. adolf
  69526. hecker
  69527. diterpenoid
  69528. irritants
  69529. cocarcinogens
  69530. adrenoceptor
  69531. adrian
  69532. adriana
  69533. adrien
  69534. adsorbed
  69535. adsorption
  69536. chemistry
  69537. mannich
  69538. bases
  69539. advanc
  69540. advance
  69541. advanced
  69542. advancesq
  69543. advances
  69544. advances
  69545. advances
  69546. amination
  69547. nitrogen
  69548. heterocycles
  69549. advances
  69550. cyclopentenone
  69551. synthesis
  69552. furans
  69553. advances
  69554. imidazole
  69555. chemistry
  69556. advances
  69557. synthesis
  69558. asymmetric
  69559. diels
  69560. alder
  69561. reactions
  69562. advances
  69563. pyridazine
  69564. chemistry
  69565. advances
  69566. selective
  69567. chemical
  69568. synthesis
  69569. complex
  69570. oligosac
  69571. advances
  69572. stereochemical
  69573. control
  69574. 13-diol
  69575. system
  69576. advances
  69577. tetramic
  69578. chemistry
  69579. advances
  69580. chemistry
  69581. heterodiene
  69582. metal
  69583. complexes
  69584. advances
  69585. chemistry
  69586. isochroman
  69587. advances
  69588. chemistry
  69589. stable
  69590. nitroxides
  69591. advances
  69592. chemistry
  69593. sulfimides
  69594. related
  69595. compound
  69596. advances
  69597. chemistry
  69598. sulphenic
  69599. amides
  69600. advances
  69601. chichibabin
  69602. reaction
  69603. advances
  69604. synthesis
  69605. alpha-methylene
  69606. lactones
  69607. advances
  69608. synthesis
  69609. biologically
  69610. active
  69611. organofluor
  69612. advances
  69613. synthesis
  69614. iodoaromatic
  69615. compounds
  69616. advances
  69617. synthesis
  69618. oligonucleotides
  69619. phospho
  69620. advances
  69621. synthesis
  69622. substituted
  69623. pyridazines
  69624. advantage
  69625. adventure
  69626. adventures
  69627. advnnces
  69628. aerobic
  69629. afanas'ev
  69630. afanasiev
  69631. afarinkia
  69632. afarinkia
  69633. kamyar
  69634. membered
  69635. heterocycles
  69636. containing
  69637. afarinkia
  69638. kamyar
  69639. vinader
  69640. victoria
  69641. nelson
  69642. posner
  69643. affecting
  69644. affinities
  69645. affinity
  69646. afford
  69647. afforded
  69648. affording
  69649. afghijk
  69650. aflatoxin
  69651. african
  69652. after
  69653. afterglow
  69654. afzal
  69655. afzal
  69656. hassan
  69657. masad
  69658. absorption
  69659. spectra
  69660. afzal
  69661. hassan
  69662. proton
  69663. magnetic
  69664. resonance
  69665. spectra
  69666. agababyan
  69667. agafonov
  69668. against
  69669. agamey
  69670. agami
  69671. agaric
  69672. agent
  69673. agents
  69674. david
  69675. michael
  69676. methodology
  69677. establish
  69678. david
  69679. michael
  69680. synthesis
  69681. carbohydrate
  69682. aggarwal
  69683. aggarwal
  69684. varinder
  69685. kumar
  69686. enantioselective
  69687. transformations
  69688. aggregates
  69689. aggregation
  69690. aggregative
  69691. agharahimi
  69692. aglycon
  69693. aglycone
  69694. agments
  69695. agonist
  69696. agonistic
  69697. agonists
  69698. agosta
  69699. agrawal
  69700. agrawal
  69701. sudhir
  69702. protocols
  69703. oligonucleotides
  69704. analogs
  69705. agricultural
  69706. agrofogliop
  69707. agrofoglio
  69708. suhas
  69709. farese
  69710. condom
  69711. challand
  69712. aguero
  69713. aguilera
  69714. agullo
  69715. ahlberg
  69716. ahmad
  69717. ahmar
  69718. ahmar
  69719. duyck
  69720. fleming
  69721. stereocontrol
  69722. using
  69723. silicon
  69724. ahmed
  69725. ahrens
  69726. ahuja
  69727. aided
  69728. aids-driven
  69729. aids-driven
  69730. nucleoside
  69731. chemistry
  69732. aiello
  69733. aiienic
  69734. aikaloids
  69735. aikoxy
  69736. aikyl
  69737. aikylation
  69738. air-water
  69739. aitken
  69740. aitken
  69741. kilenyi
  69742. asymmetric
  69743. synthesis
  69744. blackie
  69745. aitken
  69746. armstrong
  69747. david
  69748. mesher
  69749. shaun
  69750. oxidation
  69751. ajmalicine
  69752. ajmaline
  69753. akademiai
  69754. akelab
  69755. akelab
  69756. sherrington
  69757. application
  69758. functionalized
  69759. polym
  69760. akelah
  69761. akelah
  69762. heterogeneous
  69763. organic
  69764. synthesis
  69765. using
  69766. functionalize
  69767. akermark
  69768. akgun
  69769. akhmedov
  69770. akhmetova
  69771. akhrem
  69772. akhtar
  69773. akhtar
  69774. jones
  69775. biological
  69776. transformations
  69777. involving
  69778. unsatu
  69779. akhtar
  69780. wright
  69781. unified
  69782. mechanistic
  69783. oxidative
  69784. akiba
  69785. akiba
  69786. inamoto
  69787. chemistry
  69788. nitrosoimines
  69789. akihiko
  69790. akihito
  69791. akimoto
  69792. akira
  69793. akitt
  69794. akiya
  69795. akiyama
  69796. akkerman
  69797. akmori
  69798. akse'nov
  69799. akse'nov
  69800. vlasov
  69801. shnitko
  69802. intercalation
  69803. compounds
  69804. aksenov
  69805. aksenov
  69806. terent'eva
  69807. savinykh
  69808. nucleophilic
  69809. substi
  69810. akulov
  69811. akulov
  69812. kinetic
  69813. isotope
  69814. effects
  69815. enzymic
  69816. reactions
  69817. al'bina
  69818. al/pb/ni
  69819. alain
  69820. alane
  69821. alanine
  69822. alantolactones
  69823. alauddin
  69824. albano
  69825. alberg
  69826. albericio
  69827. albers
  69828. albersheim
  69829. albert
  69830. alberto
  69831. albery
  69832. albery
  69833. kreevoy
  69834. methyl
  69835. transfer
  69836. reactions
  69837. albini
  69838. albini
  69839. photosensitization
  69840. organic
  69841. synthesis
  69842. albini
  69843. fasani
  69844. elisa
  69845. mella
  69846. mariella
  69847. reactions
  69848. albini
  69849. angelo
  69850. mella
  69851. mariella
  69852. freccero
  69853. mauro
  69854. method
  69855. albini
  69856. angelo
  69857. synthetic
  69858. utility
  69859. amine
  69860. oxides
  69861. synthesis
  69862. albizati
  69863. albizati
  69864. martin
  69865. agharahimi
  69866. stolze
  69867. bioorg
  69868. albizati's
  69869. albrecht
  69870. albrecht
  69871. albrecht
  69872. harry
  69873. christenson
  69874. james
  69875. mechanism
  69876. based
  69877. albright
  69878. albright
  69879. halevi
  69880. guidelines
  69881. presentation
  69882. alcermark
  69883. alcohol
  69884. ol-promoted
  69885. alcoholic
  69886. alcoholsH
  69887. alcohols
  69888. alcohols
  69889. phenols
  69890. ethers
  69891. alcoholysis
  69892. aldehyde
  69893. hydes
  69894. aldehydes
  69895. introduction
  69896. alderw
  69897. alder
  69898. alderweireldt
  69899. aldhydes
  69900. aldimine
  69901. aldimines
  69902. aldohexoses
  69903. aldol
  69904. lable
  69905. aldol
  69906. reactions
  69907. dibenzylamino
  69908. ethyl
  69909. ketones
  69910. aldol
  69911. reactions
  69912. methyl
  69913. tributylstannyl
  69914. tetrahydrofuran
  69915. aldols
  69916. aldoses
  69917. aldoshin
  69918. aldosides
  69919. aldous
  69920. aldoximes
  69921. aldrichimica
  69922. aldridge
  69923. alefounder
  69924. aleksandrov
  69925. aleksandrov
  69926. tarunin
  69927. oxidation
  69928. ozone
  69929. hetero
  69930. alekseev
  69931. alekseeva
  69932. aleksei
  69933. aleshkova
  69934. aleskerov
  69935. aleskerov
  69936. yufit
  69937. kucherov
  69938. mechanism
  69939. alessandro
  69940. alexakis
  69941. alexakis
  69942. stereochemical
  69943. aspects
  69944. formation
  69945. alexakis
  69946. alexandre
  69947. mangeney
  69948. pierre
  69949. chiral
  69950. acetals
  69951. asymmet
  69952. alexander
  69953. alexander
  69954. alexandra
  69955. alexandre
  69956. alexandru
  69957. alexanian
  69958. alexey
  69959. alfimov
  69960. alfons
  69961. alfred
  69962. alfredo
  69963. algae
  69964. algal
  69965. alhenyl
  69966. alicyclicW
  69967. alides
  69968. aliette
  69969. alignment
  69970. alina
  69971. alipbatic
  69972. aliphati
  69973. aliphatic
  69974. aliphatic
  69975. fluorine-containing
  69976. amino
  69977. acids
  69978. aliphatic
  69979. organophosphorus
  69980. nitro-compounds
  69981. ality
  69982. alkadienals
  69983. alkadienes
  69984. alkadienyl
  69985. alkadiynes
  69986. alkali
  69987. alkali
  69988. metal
  69989. addition
  69990. unsaturated
  69991. systems
  69992. alkali
  69993. metal
  69994. fluorides
  69995. organic
  69996. synthesis
  69997. alkali
  69998. metals
  69999. alkali-metal
  70000. alkaline
  70001. alkaliods
  70002. alkaloi
  70003. alkaloid
  70004. alkaloids{
  70005. alkaloids
  70006. alkaloids
  70007. alkaloids-with
  70008. alkan-3-ones
  70009. alkanals
  70010. alkane
  70011. alkanediols
  70012. alkanes
  70013. alkanesulfonyl
  70014. alkanethiols
  70015. alkanols
  70016. alkanonones
  70017. alkanoyl
  70018. alkapolyenylidenecar
  70019. alken
  70020. alkenals
  70021. alkenamides
  70022. alkene
  70023. alkene
  70024. adducts
  70025. cyclic
  70026. thiazenes
  70027. identification
  70028. alkene
  70029. alkyne
  70030. metathesis
  70031. reactions
  70032. alkene
  70033. diazonium
  70034. salts
  70035. chapter
  70036. classical
  70037. organic
  70038. alkene
  70039. metathesis
  70040. related
  70041. reactions
  70042. alkene
  70043. synthesis
  70044. alkene-forming
  70045. alkenediazonium
  70046. alkenenitriles
  70047. alkenesH
  70048. lkenes
  70049. tosylhydrazones
  70050. alkenes
  70051. photooxidation
  70052. alkenic
  70053. alkenoates
  70054. alkenolides
  70055. alkenvl
  70056. alkenyl
  70057. alkenyl
  70058. radical
  70059. cations
  70060. alkenylalanes
  70061. alkenylanilines
  70062. alkenylation
  70063. alkenylboranes
  70064. alkenylborinates
  70065. alkenylboronic
  70066. alkenylcycloalkan
  70067. alkenylcyclobutenedi
  70068. alkenylhydroxylamine
  70069. alkenylidene
  70070. alkenyllithiums
  70071. alkenylmercurials
  70072. alkenyloxazolidines
  70073. alkenylphenols
  70074. alkenylstannanes
  70075. alkenyltrimethylstan
  70076. alkenylzinc
  70077. alkenylzirconocene
  70078. nylenamines
  70079. alklycarbene
  70080. alkoloid
  70081. alkoxide
  70082. alkoxide
  70083. clusters
  70084. molybdenum
  70085. tungsten
  70086. templates
  70087. alkoxides
  70088. alkoxo
  70089. alkoxy
  70090. alkoxy
  70091. alkoxy
  70092. radicals
  70093. organic
  70094. synthesis
  70095. novel
  70096. approach
  70097. alkoxyacetylenes
  70098. alkoxyacroleins
  70099. alkoxyacrylates
  70100. alkoxyaldehyde
  70101. alkoxyalkenylstannan
  70102. alkoxyalkenylzincs
  70103. alkoxyalkyllithiums
  70104. alkoxyallenes
  70105. alkoxyallenes-buildi
  70106. alkoxyallenes-buildi
  70107. blocks
  70108. organic
  70109. synthesis
  70110. alkoxyallylic
  70111. alkoxyaluminohydride
  70112. alkoxyaluminum
  70113. alkoxyanilines
  70114. alkoxyazetidin
  70115. alkoxybutenolides
  70116. alkoxycarbene
  70117. alkoxycarbonyl
  70118. alkoxycarbonyl/sulfi
  70119. alkoxycarbonylamino
  70120. alkoxycarbonylation
  70121. alkoxycarbonylmethyl
  70122. alkoxycarbonyloxazol
  70123. alkoxyiodination
  70124. alkoxyketenes
  70125. alkoxyl
  70126. alkoxylipids
  70127. alkoxymethyl
  70128. alkoxyoxazole
  70129. alkoxypropenes
  70130. alkoxyquinolinequino
  70131. alkoxysulfonium
  70132. alkoxytrimethylsilan
  70133. alkyations
  70134. alkyl
  70135. metal
  70136. amides
  70137. alkyl
  70138. anions
  70139. alkyl
  70140. heteroaryl
  70141. peroxides
  70142. alkyl
  70143. hydroperoxides
  70144. alkyl
  70145. iminoacyl
  70146. peroxides
  70147. alkyl
  70148. metal
  70149. peroxides
  70150. alkyl
  70151. organoelement
  70152. peroxides
  70153. alkyl
  70154. vinyl
  70155. peroxides
  70156. alkyl-radical
  70157. alkyl-substituted
  70158. alkylalk
  70159. alkylamine
  70160. alkylamines
  70161. alkylamino
  70162. alkylaromatics
  70163. alkylaryl
  70164. alkylated
  70165. alkylating
  70166. alkylationt
  70167. aldol
  70168. reaction
  70169. lactic
  70170. glycolic
  70171. alkylation
  70172. ambident
  70173. nucleophilic
  70174. hydroxamates
  70175. 4-suhs
  70176. alkylation
  70177. chiral
  70178. hydrazones
  70179. alkylation
  70180. imine
  70181. enamine
  70182. salts
  70183. alkylation
  70184. ketones
  70185. aldehydes
  70186. their
  70187. nitrogen
  70188. deriv
  70189. alkylation
  70190. reactions
  70191. thioamides
  70192. alkylation
  70193. vinylogous
  70194. alkylations
  70195. alkylations
  70196. alkynyl
  70197. carbanions
  70198. alkylations
  70199. enols
  70200. enolates
  70201. alkylations
  70202. nitrogen-stabilized
  70203. carbanions
  70204. alkylations
  70205. other
  70206. heteroatom-stabilize
  70207. carbanions
  70208. alkylations
  70209. sulfur
  70210. selenium-containing
  70211. carbanions
  70212. alkylations
  70213. vinyl
  70214. carbanions
  70215. alkylative
  70216. alkylbenzene
  70217. alkylbenzenes
  70218. alkylcopper
  70219. alkylcyclopropenes
  70220. alkyldiamino
  70221. alkyldiphenylphosphi
  70222. alkylheteroaromatics
  70223. alkylheteroaromatics
  70224. building
  70225. blocks
  70226. synthesis
  70227. alkylidenation
  70228. alkylidene
  70229. alkylidene
  70230. carbenes
  70231. intermediates
  70232. synthesis
  70233. alkylidene
  70234. complexes
  70235. niobium
  70236. antalum
  70237. alkylidene-13-dicarb
  70238. alkylidenecarbenes
  70239. alkylidenecycloalkan
  70240. alkylations
  70241. alkylations
  70242. alkynyl
  70243. carbanions@
  70244. alkylidenecyclopropa@
  70245. alkylthionitroso
  70246. arylthionitroso
  70247. compounds
  70248. generated
  70249. alkynyl
  70250. alkenyl
  70251. phenyl
  70252. iodonium
  70253. compounds@
  70254. allene
  70255. epoxidation
  70256. oxidative
  70257. cyclizations
  70258. allenyl
  70259. acides@
  70260. 13-strain
  70261. controlling
  70262. factor
  70263. stereoselective@
  70264. allylsilanes
  70265. organic
  70266. synthesis@
  70267. alpha
  70268. alpha-amidoalkylatio
  70269. carbon
  70270. recent
  70271. advances@
  70272. alpha-fluorocarbonyl
  70273. compounds
  70274. related
  70275. chemistry@
  70276. alpha-oxo
  70277. ketene
  70278. dithioacetals
  70279. related
  70280. compounds
  70281. versati@
  70282. alternative@
  70283. amaryllidaceae
  70284. amides
  70285. amination
  70286. amines
  70287. amino
  70288. amino
  70289. peptide
  70290. synthesis@
  70291. aminoalkylcarboxylic
  70292. aminohaloborane
  70293. organic
  70294. synthesis
  70295. specific
  70296. ortho
  70297. substi@
  70298. among
  70299. approach
  70300. stable
  70301. organic
  70302. molecules
  70303. triplet
  70304. state@
  70305. efficient
  70306. synthesis
  70307. tetrahydroisoquinoli@
  70308. alkylidenecyclopropa
  70309. alkylidenecyclopropa
  70310. related
  70311. compounds
  70312. alkylidenecyclopropa
  70313. strained
  70314. polar
  70315. aromatics
  70316. alkylidenediorganote
  70317. alkylideneglycinamid
  70318. alkylidenephosphoran
  70319. alkylidenesulfonium
  70320. alkylidenesulfuranes
  70321. alkylidenesulfuranes
  70322. alkylidenethiocarbon
  70323. alkylidenetriazanes
  70324. alkylidenetriazanes
  70325. triazenes
  70326. higher
  70327. homologues
  70328. alkylidenophosphoran
  70329. alkylidienephosphora
  70330. alkylidyne
  70331. alkylimidazoles
  70332. alkyliodine
  70333. alkyllithium
  70334. alkyllithiums
  70335. alkylmercurials
  70336. alkylperoxy
  70337. alkylperoxy
  70338. esters
  70339. inorganic
  70340. oxyacids
  70341. alkylphosphonic
  70342. alkylpyridines
  70343. alkylquinolines
  70344. alkyls
  70345. alkylserine
  70346. alkylsilanes
  70347. alkylsulfamoyl
  70348. alkylsulfinyl
  70349. alkylthio
  70350. alkylthioethylenic
  70351. alkylthionitroso
  70352. alkylthionitroso
  70353. arylthionitroso
  70354. compounds
  70355. generated
  70356. alkylthiophenes
  70357. alkyltransition
  70358. alkyltributylstannan
  70359. alkylzinc
  70360. alkynals
  70361. alkyne
  70362. alkyne-derived
  70363. alkynesC
  70364. alkynoates
  70365. alkynols
  70366. alkynoyl
  70367. alkynylC
  70368. alkynyl
  70369. alkenyl
  70370. phenyl
  70371. iodonium
  70372. compounds
  70373. alkynyl
  70374. carbo
  70375. ylate
  70376. phosphate
  70377. sulfonate
  70378. esters
  70379. alkynyl
  70380. cations
  70381. alkynylalkoxycarbene
  70382. alkynylaluminium
  70383. alkynylaluminum
  70384. alkynylamines
  70385. alkynylation
  70386. alkynylcarbene
  70387. alkynylesters
  70388. alkynyliodonium
  70389. alkynylpalladium
  70390. alkynylpyridazines
  70391. alkynylsilane
  70392. alkynylsilane-termin
  70393. alkynyltins
  70394. allaf
  70395. allah
  70396. allakhverdiev
  70397. allan
  70398. allelochemicals
  70399. allen
  70400. allen
  70401. angela
  70402. vaillancourt
  70403. valerie
  70404. albizati
  70405. furanoses
  70406. allene
  70407. xidation
  70408. oxidative
  70409. cyclizations
  70410. allenyl
  70411. acides
  70412. allenecarboxylate
  70413. allenes
  70414. allenes
  70415. allenes
  70416. partners
  70417. intramolecular
  70418. cobalt
  70419. mediated
  70420. allenes
  70421. bromo
  70422. benzopyrans
  70423. allenes
  70424. organic
  70425. synthesis
  70426. allenic
  70427. allenmark
  70428. allenyl
  70429. allenylcarbinols
  70430. allenylethers
  70431. allenylidene
  70432. ylmethyl
  70433. allenylmethylaniline
  70434. allenylphenols
  70435. allenylsilane
  70436. allenylsilanes
  70437. allergy
  70438. allerhand
  70439. allerhand
  70440. natural
  70441. abundance
  70442. carbon
  70443. spectroscopy
  70444. allied
  70445. allinger
  70446. allium
  70447. allkyl
  70448. allopumiliotoxin
  70449. allopumiliotoxins
  70450. allosamizoline
  70451. allotrope
  70452. allotropes
  70453. allotropic
  70454. allowed
  70455. alloy
  70456. alloy
  70457. alloyohimbane
  70458. alloys
  70459. allyl
  70460. allyl
  70461. nickel
  70462. halides
  70463. selective
  70464. reagents
  70465. organic
  70466. synthe
  70467. allyl
  70468. organometallics
  70469. allyl-metal
  70470. allylamines
  70471. allylation
  70472. allylation
  70473. halides
  70474. adjacent
  70475. diene
  70476. allylation
  70477. pummerer
  70478. generated
  70479. substituted
  70480. vinylthionium
  70481. allylbarium
  70482. allylbarium
  70483. reagents
  70484. unprecedented
  70485. regio
  70486. stereoselective
  70487. allylboranes
  70488. allylboration
  70489. allylboronates
  70490. allylcobalt
  70491. allylester
  70492. allyli
  70493. allylicC
  70494. controlling
  70495. factor
  70496. stereoselective
  70497. allylic
  70498. 13-strain
  70499. controlling
  70500. factor
  70501. stereoselective
  70502. allylic
  70503. benzylic
  70504. carbanions
  70505. substitut
  70506. heteroatoms
  70507. allylic
  70508. sulfones
  70509. allyl
  70510. anion
  70511. equivalents
  70512. homoallylic
  70513. allylic
  70514. sulphoxides
  70515. useful
  70516. intermediates
  70517. organic
  70518. synthesi
  70519. allylic
  70520. compounds
  70521. organic
  70522. synthesis
  70523. allylidene
  70524. allylidenecyclopropa
  70525. allylidenetriphenylp
  70526. allylidenetriphenylp
  70527. bifunctional
  70528. reagent
  70529. synthesis
  70530. allylindium
  70531. indoles
  70532. allylketene
  70533. allylmagnesium
  70534. allylmetal
  70535. allylmetal
  70536. derivatives
  70537. organic
  70538. synthesis
  70539. allylnickel
  70540. allyloxy
  70541. allyloxyindoles
  70542. allylpalladium
  70543. allylperoxyl
  70544. allylphenyl
  70545. allylsilane
  70546. allylsilanes
  70547. allylsilanes
  70548. allylstannanes
  70549. related
  70550. systems
  70551. allylsilanes
  70552. organic
  70553. synthesis
  70554. allylsilanes
  70555. organic
  70556. synthesis
  70557. method
  70558. introduc
  70559. allylsiloanes
  70560. allylstannane-aldehy
  70561. allylstannanes
  70562. allylsulfonium
  70563. allylsulfonyl
  70564. allyltin
  70565. allyltrimethylsilane
  70566. allyltriphenyl
  70567. allylzirconation
  70568. allylzirconocene
  70569. allysilanes
  70570. almerico
  70571. almond
  70572. almond
  70573. photooxidation
  70574. reactions
  70575. transition
  70576. metal
  70577. aloids
  70578. alois
  70579. along
  70580. alpatova
  70581. alpegiani
  70582. alpegiani
  70583. marco
  70584. bissolino
  70585. pierluigi
  70586. borghi
  70587. daniela
  70588. sbraletta
  70589. alper
  70590. alper
  70591. oxidation
  70592. reduction
  70593. rearrangement
  70594. other
  70595. syntheti
  70596. alper
  70597. phase
  70598. transfer
  70599. catalysis
  70600. organometallic
  70601. chemistry
  70602. alper
  70603. howard
  70604. simple
  70605. novel
  70606. methods
  70607. synthesis
  70608. carbo
  70609. alpha
  70610. alpha
  70611. alpha
  70612. amidoalkylations
  70613. carbon
  70614. harold
  70615. zaugg
  70616. william
  70617. alpha
  70618. amino
  70619. hydroxy
  70620. acids
  70621. total
  70622. synthesis
  70623. alpha
  70624. beta-epoxysilanes
  70625. alpha
  70626. beta-unsaturated
  70627. carbonyls
  70628. alpha
  70629. heteroatom
  70630. substituted
  70631. radicals
  70632. alpha
  70633. metallo
  70634. amine
  70635. synthetic
  70636. equivalents
  70637. alpha
  70638. nitroketones
  70639. stereochemistry
  70640. nitration
  70641. alpha'-diheterosubst
  70642. alpha'-position
  70643. alpha-acylcarbenium
  70644. alpha-acylcarbenium
  70645. alpha-alkylation
  70646. alpha-amidoalkylatio
  70647. alpha-amidoalkylatio
  70648. carbon
  70649. alpha-amidoalkylatio
  70650. carbon
  70651. recent
  70652. advances
  70653. alpha-amino
  70654. alpha-amino
  70655. synthesis
  70656. alpha-amino-beta-hyd
  70657. alpha-amino-beta-hyd
  70658. acids
  70659. total
  70660. synthesis
  70661. amino
  70662. alpha-aminocarbonyl
  70663. alpha-aminocarbonyl
  70664. related
  70665. compounds
  70666. syntheses
  70667. alpha-and
  70668. alpha-arylprop
  70669. alpha-boron
  70670. alpha-carbon
  70671. alpha-carbonyl
  70672. alpha-carbonyl
  70673. cations
  70674. alpha-carboxamide
  70675. alpha-carboxamide
  70676. function
  70677. peptides
  70678. alpha-carboxy
  70679. alpha-chiral
  70680. alpha-chiral
  70681. allylboronates
  70682. reagents
  70683. asymmetric
  70684. synthesi
  70685. alpha-chlorosulfides
  70686. alpha-cleavage
  70687. alpha-cyano
  70688. alpha-cyanothioaceta
  70689. alpha-cyclopiazonic
  70690. alpha-diazo
  70691. alpha-diazocarbonyl
  70692. alpha-diazoketones
  70693. alpha-dihetero
  70694. alpha-diones
  70695. alpha-diones
  70696. cyclic
  70697. oxamides
  70698. organolithium
  70699. reagents
  70700. alpha-effect
  70701. alpha-fluorocarbonyl
  70702. alpha-fluorocarbonyl
  70703. compounds
  70704. related
  70705. chemistry
  70706. alpha-functionalizat
  70707. alpha-halo
  70708. alpha-halo-alpha-nit
  70709. alpha-halo-alpha-nit
  70710. acids
  70711. their
  70712. derivatives
  70713. alpha-haloalkyl
  70714. alpha-haloboronic
  70715. alpha-haloboronic
  70716. esters
  70717. intermediates
  70718. stereodirected
  70719. alpha-halogeno
  70720. alpha-halogeno-organ
  70721. alpha-halogenonitroa
  70722. alpha-helix
  70723. alpha-hetero
  70724. alpha-hetero
  70725. alpha
  70726. alpha-dihetero
  70727. triheteromethyl
  70728. anions
  70729. alpha-hetero
  70730. alpha
  70731. alpha'-diheterosubst
  70732. dialkylperoxides
  70733. alpha-heterosubstitu
  70734. alpha-heterosubstitu
  70735. alkyl
  70736. hydroperoxides
  70737. alpha-hydroxy
  70738. alpha-hydroxylamino
  70739. alpha-keto
  70740. alpha-metal
  70741. alpha-metal
  70742. substituted
  70743. carbanions
  70744. alpha-metalated
  70745. alpha-metalated
  70746. isocyanides
  70747. organic
  70748. synthesis
  70749. alpha-metallo
  70750. alpha-methylene
  70751. alpha-nitroketones
  70752. alpha-nitronitriles
  70753. alpha-oxo
  70754. alpha-oxo
  70755. ketene
  70756. dithioacetals
  70757. related
  70758. compounds
  70759. versati
  70760. alpha-oxoketene-s
  70761. alpha-oxoketene-s
  70762. n-acetals
  70763. versatile
  70764. intermedia
  70765. alpha-oxoketenes
  70766. alpha-oxoketenes
  70767. preparation
  70768. chemistry
  70769. alpha-peroxy
  70770. alpha-peroxyamines
  70771. alpha-phosphonate
  70772. alpha-phosphonate
  70773. carbanions
  70774. simple
  70775. reactions
  70776. alpha-pinene
  70777. alpha-silyl
  70778. alpha-substituted
  70779. alpha-sulfinyl
  70780. alpha-sulphenylated
  70781. alpha-sulphenylated
  70782. carbonyl
  70783. compounds
  70784. synthesis
  70785. alpha-thiocarbocatio
  70786. alpha-ureidoalkylati
  70787. alpha-x-alkenyl
  70788. alpha-x-alkyl
  70789. alpha-x-alkyl
  70790. alpha-x-alkenyl
  70791. yltellurium
  70792. compounds
  70793. alpha-zirconocenyl
  70794. alphaca
  70795. alphatic
  70796. alpine
  70797. alsters
  70798. altered
  70799. altering
  70800. altering
  70801. stereochemistry
  70802. allylation
  70803. reactions
  70804. alternant
  70805. alternate
  70806. alternating
  70807. alternative
  70808. alternative
  70809. synthetic
  70810. approaches
  70811. euryfuran
  70812. furan
  70813. alternatively
  70814. alternatives
  70815. altona
  70816. altria
  70817. alumina
  70818. aluminide
  70819. aluminium
  70820. alumino
  70821. aluminum
  70822. aluminum
  70823. amineplexes
  70824. conversion
  70825. carboxylic
  70826. esters
  70827. alvarez
  70828. alvarez
  70829. mercedes
  70830. joule
  70831. synthesis
  70832. pyridoacridines
  70833. alvarez
  70834. mercedes
  70835. salas
  70836. marisa
  70837. joule
  70838. marine
  70839. nitrogen
  70840. alves
  70841. alwarsamy
  70842. alyzed
  70843. alzheimer's
  70844. amabilino
  70845. david
  70846. stoddart
  70847. fraser
  70848. assembly
  70849. macrom
  70850. amalgam
  70851. amalgam
  70852. reductions
  70853. amalia
  70854. amanita
  70855. amarnath
  70856. amaryllidaceae
  70857. amaryllidaceae
  70858. amaryllidaceae
  70859. sceletium
  70860. alkaloids
  70861. amaryllidaceen
  70862. amato
  70863. amatore
  70864. amberlyst
  70865. amberlyst
  70866. versatile
  70867. catalyst
  70868. silicon
  70869. terminated
  70870. ambident
  70871. ambident
  70872. heterocyclic
  70873. reactivity
  70874. alkylation
  70875. substituted
  70876. ambident
  70877. heterocyclic
  70878. reactivity
  70879. alkylation
  70880. substituted
  70881. ambient
  70882. ambient
  70883. temperature
  70884. unsymmetrical
  70885. biaryl
  70886. synthesis
  70887. using
  70888. ambroz
  70889. ambroz
  70890. cations
  70891. light
  70892. intermedia
  70893. ambruticine
  70894. amelioration
  70895. american
  70896. americanchemicalsoci
  70897. amide
  70898. ecting
  70899. radical
  70900. translocating
  70901. groups
  70902. amide-amide
  70903. amides
  70904. amides
  70905. amidese
  70906. amidine
  70907. amidines
  70908. amidoalkylation
  70909. amidoalkylation
  70910. reactions
  70911. carbon
  70912. amidoalkylations
  70913. amidogen
  70914. amidoketones
  70915. amidoximes
  70916. amidoxines
  70917. amidrazone
  70918. amidrazone
  70919. analogues
  70920. ribofuranose
  70921. transition
  70922. state
  70923. amidrazones
  70924. amidyl
  70925. amidyl
  70926. carbamyl
  70927. radicals
  70928. stannane
  70929. mediated
  70930. cleavage
  70931. amimocyclopentitiol
  70932. aminal
  70933. aminals
  70934. aminating
  70935. amination
  70936. amination
  70937. amination
  70938. alkenes
  70939. amination
  70940. arenes
  70941. electron
  70942. deficient
  70943. azodicarboxylate
  70944. amination
  70945. electron-rich
  70946. substrates
  70947. photochemical
  70948. amination
  70949. nitroazaaromatics
  70950. amination
  70951. alkenylphenols
  70952. alkylamines
  70953. photoindu
  70954. aminations
  70955. amine
  70956. chlorides
  70957. amine
  70958. oxides
  70959. amine-enone
  70960. amineplexes
  70961. aminesE
  70962. amines
  70963. hydride
  70964. donors
  70965. reactions
  70966. unsatu
  70967. amines
  70968. amides
  70969. aminium
  70970. aminor
  70971. amino
  70972. synthesis
  70973. amino
  70974. derived
  70975. chiral
  70976. nitroso
  70977. compounds
  70978. diastereose
  70979. amino
  70980. esters
  70981. chiral
  70982. auxiliaries
  70983. asymmetric
  70984. cycloa
  70985. amino
  70986. acids
  70987. amino
  70988. acids
  70989. their
  70990. derivatives
  70991. amino
  70992. acids
  70993. mushrooms
  70994. amino
  70995. carbene
  70996. complexes
  70997. cascade
  70998. reactions
  70999. amino-b
  71000. amino-protecting
  71001. amino236
  71002. aminoacetals
  71003. aminoacetylenes
  71004. aminoacid
  71005. aminoacids
  71006. aminoacids
  71007. cyclobutane
  71008. series
  71009. aminoacids
  71010. peptides
  71011. heterocyclic
  71012. chemistry
  71013. aminoacyl
  71014. aminoalcohols
  71015. aminoaldehydes
  71016. aminoalkanoates
  71017. aminoalkyl
  71018. aminoalkylcarboxylic
  71019. aminoalkylcarboxylic
  71020. aminoalkylheterocycl~
  71021. aminoalkylphosphonic
  71022. aminoamide
  71023. aminoamides
  71024. aminoarenes
  71025. aminoarsanes
  71026. aminoarsanes
  71027. reparative
  71028. reagents
  71029. aminoaryl
  71030. aminoaziridinylhydra
  71031. aminoazonium
  71032. aminobenzannulation
  71033. aminobenzannulation
  71034. metathesis
  71035. isonitriles
  71036. using
  71037. aminobenzimidazoles
  71038. aminobenzonitriles
  71039. aminobenzophenones
  71040. aminobenzotriazoles
  71041. aminobenzyl
  71042. aminobicyclo
  71043. aminobut
  71044. aminobutanoate
  71045. aminobutyric
  71046. aminocarbene
  71047. aminocarbene
  71048. complexes
  71049. chromium
  71050. molybdenum
  71051. initiators
  71052. aminocarbonyl
  71053. aminocarbonylazoalke
  71054. aminocoumarins
  71055. aminocyclopentitols
  71056. aminocyclopropanes
  71057. aminodeoxy
  71058. aminoethyl
  71059. aminofluorosulfurane
  71060. aminofurazans
  71061. aminoglycoside
  71062. aminoglycosides
  71063. aminohaloborane
  71064. aminohaloborane
  71065. organic
  71066. synthesis
  71067. specific
  71068. ortho
  71069. substi
  71070. aminoheterocycles
  71071. aminohydroxylation
  71072. aminoketones
  71073. aminolysis
  71074. aminomethyl
  71075. aminomethylenemalona
  71076. aminomethylenemalona
  71077. their
  71078. heterocyclic
  71079. synthesis
  71080. aminonitrenes
  71081. aminonitrile
  71082. aminonitriles
  71083. aminophoaphinates
  71084. aminophosphinocarbox
  71085. aminophosphonates
  71086. aminophosphonates
  71087. aminophoaphinates
  71088. synthesis
  71089. proper
  71090. aminopyrazoles
  71091. aminostannanes
  71092. aminosuccinimide
  71093. aminothioacrylamides
  71094. aminyl
  71095. aminyloxides
  71096. amitai
  71097. amiya
  71098. amma-halo
  71099. ammann
  71100. ammines
  71101. ammonia
  71102. ammoniumv
  71103. ammophosphinates
  71104. ammoxidation
  71105. among
  71106. among
  71107. amoore
  71108. amorphous
  71109. amoryllidaceae
  71110. amount
  71111. amounts
  71112. amphibian
  71113. amphiphilic
  71114. amphoteric
  71115. amphotericin
  71116. amphoteronolide
  71117. amplication
  71118. amplification
  71119. amplitude
  71120. amsterdamV
  71121. access
  71122. erythro
  71123. diols
  71124. sharpless's
  71125. asymmetric
  71126. dihydr
  71127. alternate
  71128. method
  71129. synthesis
  71130. secondary
  71131. nitramine
  71132. alternative
  71133. procedure
  71134. stereoselective
  71135. formation
  71136. alternative
  71137. synthesis
  71138. heteroaryl
  71139. bromides
  71140. approach
  71141. lysergic
  71142. utilizing
  71143. intramolecular
  71144. approach
  71145. stable
  71146. organic
  71147. molecules
  71148. triplet
  71149. state
  71150. approach
  71151. total
  71152. synthesis
  71153. lycoricidine
  71154. article
  71155. about
  71156. robert
  71157. burns
  71158. woodward
  71159. asymmetric
  71160. synthesis
  71161. fully
  71162. functionalized
  71163. syste
  71164. aza-brook
  71165. rearrangemnt
  71166. a-silylallyl
  71167. amine
  71168. alkalo
  71169. economical
  71170. preparation
  71171. bromoethyl
  71172. dioxane
  71173. effective
  71174. selective
  71175. synthesis
  71176. sterically
  71177. crowded
  71178. efficient
  71179. enantioselective
  71180. synthesis
  71181. chiral
  71182. efficient
  71183. general
  71184. strategy
  71185. synthesis
  71186. secon
  71187. efficient
  71188. approach
  71189. toward
  71190. taxane
  71191. analogs
  71192. atrop
  71193. diaste
  71194. efficient
  71195. deoxygenation
  71196. alkenyl
  71197. alkyl
  71198. phenyl
  71199. efficient
  71200. julia
  71201. olefination
  71202. mediated
  71203. magnesium
  71204. efficient
  71205. method
  71206. oxidation
  71207. sulfides
  71208. sulfone
  71209. efficient
  71210. procedure
  71211. vinylation
  71212. pyrrole
  71213. efficient
  71214. synthesis
  71215. butylphenyl
  71216. esters
  71217. efficient
  71218. synthesis
  71219. tetrahydroisoquinoli
  71220. efficient
  71221. synthesis
  71222. catechol
  71223. cyclic
  71224. sulfates
  71225. efficient
  71226. synthesis
  71227. crinane
  71228. using
  71229. intramolecular
  71230. efficient
  71231. synthesis
  71232. enantiopure
  71233. alkoxy
  71234. propadiene
  71235. efficient
  71236. synthesis
  71237. fenoprofen
  71238. important
  71239. antiinflam
  71240. enantioselective
  71241. approach
  71242. 3a-hydroxy-15-ripper
  71243. constru
  71244. enantioselective
  71245. approach
  71246. synthesis
  71247. manzamine
  71248. enantioselective
  71249. synthesis
  71250. cis-4-tert-butoxycar
  71251. useful
  71252. pecific
  71253. entry
  71254. indolizidines
  71255. intramolecular
  71256. expedient
  71257. stereoselective
  71258. route
  71259. perhydrophenan
  71260. expedient
  71261. palladium
  71262. mediated
  71263. route
  71264. methyl
  71265. benzofuran
  71266. expedient
  71267. route
  71268. enantiopure
  71269. allylic
  71270. alcohols
  71271. expedient
  71272. route
  71273. indole
  71274. acetic
  71275. derivatives
  71276. expeditious
  71277. approach
  71278. synthesis
  71279. chiral
  71280. butadieny
  71281. extremely
  71282. desulfurization
  71283. thiiranes
  71284. haoyun
  71285. bradshaw
  71286. jerald
  71287. izatt
  71288. macropolycyclic
  71289. haoyun
  71290. bradshaw
  71291. jerald
  71292. izatt
  71293. zhengming
  71294. improved
  71295. method
  71296. synthesis
  71297. alpha
  71298. diazo
  71299. ketones
  71300. improved
  71301. procedure
  71302. aldehyde
  71303. alkyne
  71304. homologation
  71305. improved
  71306. procedure
  71307. alkylation
  71308. aziridines
  71309. improved
  71310. procedure
  71311. preparation
  71312. dithiane
  71313. improved
  71314. procedure
  71315. synthesis
  71316. fluoromethylketon
  71317. improved
  71318. synthesis
  71319. conjugated
  71320. nitroolefins
  71321. industrial
  71322. perspective
  71323. total
  71324. synthesis
  71325. penem
  71326. antib
  71327. innocent
  71328. bystander
  71329. looks
  71330. 2-norbornyl
  71331. cation
  71332. introduction
  71333. chiral
  71334. centres
  71335. acyclic
  71336. systems
  71337. based
  71338. introduction
  71339. radicals
  71340. introduction
  71341. peptide
  71342. chemistry
  71343. introduction
  71344. synthesis
  71345. using
  71346. organocopper
  71347. reagents
  71348. investigation
  71349. palladium
  71350. catalyzed
  71351. hydrosilylation
  71352. iridium
  71353. based
  71354. catalyst
  71355. system
  71356. metathesis/isomeriza
  71357. haoyun
  71358. bradshaw
  71359. jerald
  71360. izatt
  71361. macropolycyclic
  71362. intramolecular
  71363. cyclization
  71364. phenol
  71365. derivatives
  71366. bearing
  71367. observation
  71368. cationic
  71369. influence
  71370. alkylation
  71371. unexpected
  71372. product
  71373. during
  71374. synthesis
  71375. phenylisoquinoli@
  71376. analogs@
  71377. analogy@
  71378. analysis
  71379. analysis
  71380. hydroxylamine
  71381. glycoside
  71382. linkages
  71383. structural
  71384. cons@
  71385. and/or@
  71386. andreev
  71387. kolomiets
  71388. fokin
  71389. sigmatropic
  71390. rearrange@
  71391. angela
  71392. angewandte
  71393. angus@
  71394. aniline
  71395. anionic
  71396. approaches
  71397. construction
  71398. cyclopentanoids@
  71399. anions
  71400. annulated
  71401. 15-benzodiazepines
  71402. membered
  71403. rings@
  71404. annulations@
  71405. anomeric
  71406. observation
  71407. cationic
  71408. influence
  71409. alkylation
  71410. outline
  71411. chemistry
  71412. 9-borabicyclo
  71413. 3.3.1
  71414. nonan
  71415. overview
  71416. total
  71417. synthesis
  71418. pyrrolizidine
  71419. alkaloid
  71420. oxidatively
  71421. removable
  71422. protecting
  71423. group
  71424. aldehydes
  71425. rearrangement
  71426. route
  71427. enantioselective
  71428. unexpected
  71429. reaction
  71430. inversion
  71431. olefin
  71432. geometry
  71433. unexpected
  71434. palladium
  71435. catalyzed
  71436. cyclization
  71437. carbohydr
  71438. unprecedented
  71439. cleavage
  71440. b-lactam
  71441. stereoselecti
  71442. unprecedented
  71443. expansion
  71444. macrolide
  71445. series
  71446. unusual
  71447. chromone
  71448. formation
  71449. rearrangement
  71450. unusual
  71451. selective
  71452. allyl
  71453. isomerization
  71454. chiral
  71455. unusual
  71456. trimerization
  71457. reaction
  71458. alkyne
  71459. iridium
  71460. anaerobic
  71461. analgesic
  71462. analog
  71463. analogies
  71464. analogous
  71465. analogso
  71466. analogue
  71467. analogues
  71468. analyses
  71469. analysi
  71470. analysis
  71471. analysis
  71472. hydroxylamine
  71473. glycoside
  71474. linkages
  71475. structural
  71476. analysis
  71477. organic
  71478. peroxy
  71479. compounds
  71480. analysis
  71481. organoboron
  71482. compounds
  71483. analysis
  71484. interactions
  71485. responsible
  71486. long-range
  71487. analytical
  71488. analytical
  71489. methods
  71490. determination
  71491. enantiomeric
  71492. purity
  71493. anand
  71494. anantharamaiahU
  71495. anastassios
  71496. anastassiou
  71497. anastassiou
  71498. kasmai
  71499. medium
  71500. large
  71501. large
  71502. excessi
  71503. anate
  71504. anatomy
  71505. anatoxin
  71506. ancepsenolide
  71507. anchimeric
  71508. anchimerically
  71509. anchimerically
  71510. accelerated
  71511. homolyses
  71512. ancient
  71513. ancistrocladaceae
  71514. andreae
  71515. siegfried
  71516. schmitz
  71517. ernst
  71518. electrophilic
  71519. aminations
  71520. andreas
  71521. andreev
  71522. andreev
  71523. kolomiets
  71524. sigmatropic
  71525. rearrangements
  71526. andreev
  71527. kolomiets
  71528. fokin
  71529. sigmatropic
  71530. rearrange
  71531. andrei
  71532. andreoli
  71533. andres
  71534. andreu
  71535. andreu
  71536. cecilia
  71537. beerli
  71538. branda
  71539. morgan
  71540. mendoz
  71541. andrew
  71542. andrews
  71543. andrianov
  71544. andrianov
  71545. emel'yanov
  71546. organosiloxazanes
  71547. andrianov
  71548. soucek
  71549. khananashvili
  71550. hydride
  71551. additio
  71552. andrus
  71553. andrushkevich
  71554. andrushkevich
  71555. popova
  71556. mechanism
  71557. heterogeneous
  71558. andruski
  71559. andrzej
  71560. andthe
  71561. anellated
  71562. anellated
  71563. heterophospholes
  71564. anest
  71565. anesthetic
  71566. dalrymple
  71567. grant
  71568. hoult
  71569. johnson
  71570. angel
  71571. angela
  71572. angela
  71573. angelo
  71574. angelov
  71575. angerhofer
  71576. angew
  71577. angew
  71578. nonmolecular
  71579. metal
  71580. chalcogenide
  71581. angew
  71582. directed
  71583. synthesis
  71584. biaryl
  71585. angewandte
  71586. angewandte
  71587. angewandte
  71588. angewante
  71589. angiolini
  71590. angiotensinn
  71591. angiotensin
  71592. receptor
  71593. antagonists
  71594. angkana
  71595. angle
  71596. angle
  71597. strained
  71598. cycloalkynes
  71599. angoh
  71600. angray
  71601. angucycline
  71602. angucyclines
  71603. angular
  71604. angularly
  71605. angularly-fused
  71606. angyal
  71607. stephen
  71608. composition
  71609. reducing
  71610. sugars
  71611. solut
  71612. regio
  71613. stereo
  71614. selectivities
  71615. nucleophilic
  71616. anhydrase
  71617. anhydride
  71618. anhydrides
  71619. anhydro
  71620. anhydronupharamine
  71621. anhydrous
  71622. aniline
  71623. aniline
  71624. anilines
  71625. anils
  71626. animals
  71627. anion
  71628. anion-assisted
  71629. anion-assisted
  71630. sigmatropic
  71631. rearrangements
  71632. anion-cation
  71633. anionic
  71634. roaches
  71635. construction
  71636. cyclopentanoids
  71637. anionic
  71638. cyclization
  71639. olefinic
  71640. alkyllithiums
  71641. closure
  71642. anionic
  71643. organotin
  71644. compounds
  71645. organic
  71646. synthesis
  71647. trialkylsta
  71648. anions
  71649. anions
  71650. anirudh
  71651. anisotropic
  71652. anklam
  71653. annelaction
  71654. annelated
  71655. annelation
  71656. annelations
  71657. annellated
  71658. annellation
  71659. annette
  71660. anniversary
  71661. annonaceous
  71662. annual
  71663. annual
  71664. survey
  71665. organic
  71666. reactions
  71667. selected
  71668. complexes
  71669. annular
  71670. annulated
  71671. annulated
  71672. 15-benzodiazepines
  71673. three
  71674. annulated
  71675. 15-benzodiazepines
  71676. membered
  71677. rings
  71678. annulation
  71679. ations
  71680. annulations
  71681. involving
  71682. aryne
  71683. chain
  71684. cyclizations
  71685. synthesi
  71686. annulene
  71687. annulenediones
  71688. annulenes
  71689. annuleno
  71690. annulenoannelation
  71691. annulenoannulenes
  71692. annulenopyridines
  71693. anodes
  71694. anodic
  71695. anodic
  71696. amide
  71697. oxidations
  71698. total
  71699. synthesis
  71700. a58365a
  71701. rac-a
  71702. anodic
  71703. oxidation
  71704. amines
  71705. anodic
  71706. oxidation
  71707. sulphur-containing
  71708. compounds
  71709. anologues
  71710. anomalies
  71711. anomeric
  71712. anomeric
  71713. anomeric
  71714. exo-anomeric
  71715. effects
  71716. carbohydrate
  71717. chemistry
  71718. anomeric
  71719. effect
  71720. origin
  71721. consequences
  71722. anomeric
  71723. effects
  71724. reference
  71725. review
  71726. anomeric-oxygen
  71727. anomeric-oxygen
  71728. activation
  71729. glycoside
  71730. synthesis
  71731. trich
  71732. anomoric
  71733. anomoric
  71734. effect
  71735. dithianes
  71736. organic
  71737. synthesis
  71738. japan
  71739. present
  71740. future
  71741. brandon
  71742. amino
  71743. peptide
  71744. guide
  71745. brandon
  71746. associ
  71747. another
  71748. review
  71749. alkylation
  71750. carbanions
  71751. derived
  71752. anqew
  71753. anrorc
  71754. ansamycin
  71755. ansamycins
  71756. ansheles
  71757. ansheles
  71758. pis'man
  71759. reactions
  71760. monoolefins
  71761. anshu
  71762. ansition
  71763. answer
  71764. answers
  71765. antagonistn
  71766. antagonistic
  71767. antagonists
  71768. antalum
  71769. anteunis
  71770. anthanassios
  71771. antheridic
  71772. antheridiogens
  71773. anthocyanidins
  71774. anthocyanins
  71775. anthony
  71776. anthracene
  71777. anthracenes
  71778. anthracycline
  71779. anthracyclines
  71780. anthracyclinone
  71781. anthracyclinones
  71782. anthranilic
  71783. anthranilides
  71784. anthranils
  71785. anthraquinone
  71786. anthraquinones
  71787. anthrone
  71788. anthyridines
  71789. antiO
  71790. amino
  71791. alcohols
  71792. allyl
  71793. borane
  71794. addition
  71795. aldehyde
  71796. michael
  71797. addition
  71798. cyanocuprate
  71799. tbucu
  71800. accepto
  71801. anti-1-alkene-34-dio
  71802. anti-13-polyols
  71803. anti-24
  71804. anti-aldol
  71805. anti-aldols
  71806. anti-hiv
  71807. anti-inflammatory
  71808. anti-michael
  71809. antib
  71810. antibacterial
  71811. antibacterial
  71812. antibio
  71813. antibiotic
  71814. antibiotics
  71815. antiviral
  71816. compounds
  71817. chemical
  71818. synthesis
  71819. antibodies
  71820. antibodies--designer
  71821. antibody
  71822. antibody
  71823. catalysis
  71824. carbon-carbon
  71825. formation
  71826. cleav
  71827. antibody
  71828. catalysis
  71829. carbon-carbon
  71830. formation
  71831. cleav
  71832. antibody
  71833. catalysis
  71834. difficult
  71835. chemical
  71836. transformations
  71837. antibody-targeted
  71838. anticancer
  71839. anticancer
  71840. acridone
  71841. alkaloids
  71842. antidepressant
  71843. antifeedant
  71844. antifeedants
  71845. antifilarial
  71846. antifungal
  71847. antigen
  71848. antigens
  71849. antigoni
  71850. antihypertensive
  71851. antiinflammatory
  71852. antimalarial
  71853. antimalarials
  71854. antimetabolites
  71855. antimicrobial
  71856. antimicrobialagents
  71857. antimitotic
  71858. antimonyN
  71859. antimony
  71860. chloride
  71861. efficient
  71862. catalyst
  71863. palladium
  71864. antimony
  71865. pentahalides
  71866. catalysts
  71867. friedel-crafts
  71868. antimony-templated
  71869. antimycotics
  71870. antiobiotic
  71871. antipin
  71872. antisense
  71873. antisense
  71874. oligonucleotides
  71875. therapeutic
  71876. principle
  71877. antisense
  71878. oligonucleotides
  71879. stereocontrolled
  71880. synthesis
  71881. antitumor
  71882. antitumor
  71883. substances
  71884. higher
  71885. plants
  71886. antitumour
  71887. antiviral
  71888. antkowiak
  71889. antkowiak
  71890. antkowiak
  71891. wieslaw
  71892. alkaloids
  71893. mushrooms
  71894. antngonists
  71895. anton
  71896. antonakis
  71897. antonio
  71898. antonova
  71899. anusch
  71900. anydrides
  71901. anzai
  71902. anzai
  71903. tetsuo
  71904. photosensitive
  71905. artificial
  71906. membrane
  71907. aoyama
  71908. aoyama
  71909. yasuhiro
  71910. accumulation
  71911. binding
  71912. sites
  71913. hydrogen
  71914. apangium
  71915. icolane
  71916. aplication
  71917. aplications
  71918. aplyronine
  71919. aplysin
  71920. apman
  71921. apocynaceae
  71922. apoptosis
  71923. aporphinoid
  71924. app-klingemann
  71925. apparent
  71926. apparu
  71927. appealing
  71928. appel
  71929. halstenberg
  71930. functional
  71931. group
  71932. conversions
  71933. using
  71934. appel
  71935. knoll
  71936. ruppert
  71937. phospha
  71938. alkenes
  71939. phospha
  71940. alkyne
  71941. appiications
  71942. appli
  71943. applica
  71944. applicability
  71945. applicable
  71946. applicat
  71947. applicat
  71948. redox
  71949. system
  71950. based
  71951. nitroxides
  71952. organic
  71953. application
  71954. application
  71955. application
  71956. anhydrous
  71957. hydrogen
  71958. fluoride
  71959. structura
  71960. application
  71961. lactams
  71962. synthesis
  71963. substance
  71964. application
  71965. chiral
  71966. cyclic
  71967. diols
  71968. asymmetric
  71969. synthesis
  71970. application
  71971. spectroscopy
  71972. radical
  71973. application
  71974. h4-diene
  71975. tricarbonyl
  71976. complexes
  71977. acycli
  71978. application
  71979. intramolecular
  71980. carbenoid
  71981. reactions
  71982. organic
  71983. application
  71984. intramolecular
  71985. reactions
  71986. forming
  71987. application
  71988. lanthanide
  71989. reagents
  71990. organic
  71991. synthesis
  71992. application
  71993. newer
  71994. organometallic
  71995. reagents
  71996. total
  71997. application
  71998. oxaziridine
  71999. organic
  72000. synthesis
  72001. application
  72002. phenolic
  72003. oxidation
  72004. total
  72005. synthesis
  72006. application
  72007. phosphonate
  72008. thiophosphate
  72009. analogs
  72010. application
  72011. silicon
  72012. chemistry
  72013. corticosteroid
  72014. field
  72015. application
  72016. tellurium
  72017. chemistry
  72018. sharpless
  72019. asymmetric
  72020. application
  72021. anhydrous
  72022. hydrogen
  72023. fluoride
  72024. structura@
  72025. application
  72026. gylcal
  72027. assembly
  72028. strategy
  72029. synthesis@
  72030. applications
  72031. applications
  72032. aziridines
  72033. synthesis
  72034. natural
  72035. produ@
  72036. applications
  72037. sulfoxides
  72038. asymmetric
  72039. synthesis
  72040. biolog@
  72041. applied
  72042. approach
  72043. approach
  72044. manzamine
  72045. using
  72046. intramolecular
  72047. diels
  72048. alder
  72049. approaches
  72050. approaches
  72051. synthesis
  72052. substituted
  72053. triazoles@
  72054. apsimon
  72055. total
  72056. synthesis
  72057. natural
  72058. products
  72059. arene
  72060. substitution
  72061. nucleophilic
  72062. addition
  72063. electron
  72064. arising@
  72065. aromatic
  72066. aromatization
  72067. artificial
  72068. hetaryl
  72069. alkali
  72070. metal
  72071. compounds@
  72072. arylacetates
  72073. arylnaphthalenes@
  72074. arylolefins
  72075. arynes@
  72076. asmus
  72077. stabilization
  72078. oxidized
  72079. sulfur
  72080. centers
  72081. organi@
  72082. aspects
  72083. through
  72084. annul@
  72085. application
  72086. gylcal
  72087. assembly
  72088. strategy
  72089. synthesis
  72090. application
  72091. mitsunobu
  72092. reaction
  72093. morphine
  72094. series
  72095. application
  72096. nickel
  72097. mediated
  72098. neopentyl
  72099. coupling
  72100. application
  72101. ultrasound
  72102. synthesis
  72103. applicationsP
  72104. applications
  72105. applications
  72106. cations
  72107. aziridines
  72108. synthesis
  72109. natural
  72110. produ
  72111. applications
  72112. salts
  72113. preparati
  72114. organic
  72115. chemistry
  72116. applications
  72117. diisobutylaluminium
  72118. hydride
  72119. triisobutyla
  72120. applications
  72121. endor
  72122. spectroscopy
  72123. radical
  72124. cations
  72125. applications
  72126. enzymes
  72127. synthesis
  72128. bioactive
  72129. polyol
  72130. applications
  72131. flash
  72132. vacuum
  72133. thermolysis
  72134. synthesis
  72135. applications
  72136. higher-order
  72137. mixed
  72138. organocuprates
  72139. organic
  72140. applications
  72141. intramolecular
  72142. photocycloadditions
  72143. applications
  72144. ionic
  72145. hydrogenation
  72146. organic
  72147. synthesis
  72148. applications
  72149. microwave
  72150. accelerated
  72151. organic
  72152. chemistry
  72153. applications
  72154. microwave
  72155. energy
  72156. organic
  72157. chemistry
  72158. applications
  72159. microwave
  72160. energy
  72161. organic
  72162. chemistry
  72163. applications
  72164. nickel
  72165. chromium
  72166. mediat
  72167. coupling
  72168. applications
  72169. organoboron
  72170. compounds
  72171. overview
  72172. applications
  72173. organometallic
  72174. reagents
  72175. lactam
  72176. chemistry
  72177. applications
  72178. oxaziridines
  72179. organic
  72180. synthesis
  72181. applications
  72182. phase
  72183. transfer
  72184. catalysis
  72185. organic
  72186. synthesi
  72187. applications
  72188. photosensitive
  72189. protecting
  72190. groups
  72191. carbohyd
  72192. applications
  72193. liver
  72194. esterase
  72195. asymmetric
  72196. synthesis
  72197. applications
  72198. liver
  72199. esterases
  72200. asymmetric
  72201. synthe
  72202. applications
  72203. solid-state
  72204. reactions
  72205. alkylation
  72206. esterif
  72207. applications
  72208. sulfoximines
  72209. synthesis
  72210. applieations
  72211. applied
  72212. applied
  72213. applied
  72214. applying
  72215. appraisal
  72216. approach
  72217. approach
  72218. using
  72219. intramolecular
  72220. diels
  72221. alder
  72222. approachesr
  72223. approaches
  72224. aches
  72225. synthesis
  72226. substituted
  72227. triazoles
  72228. approaches
  72229. synthesis
  72230. antitumor
  72231. pyridocarbazole
  72232. approaches
  72233. synthesis
  72234. pyridocarbazole
  72235. alkaloids
  72236. approaching
  72237. approximate
  72238. aprotic
  72239. aprotic
  72240. organic
  72241. superacids-efficient
  72242. reagents
  72243. catalysts
  72244. apsimon
  72245. apsimon
  72246. blackwell
  72247. edwards
  72248. fruchier
  72249. miller
  72250. apsimon
  72251. seguin
  72252. recent
  72253. advances
  72254. asymmetric
  72255. synthes
  72256. apsimon
  72257. total
  72258. synthesis
  72259. natural
  72260. products
  72261. apsimon
  72262. total
  72263. synthesis
  72264. natural
  72265. products
  72266. aptitudes
  72267. apushkinskii
  72268. aqueous
  72269. cycloadditions
  72270. using
  72271. glycoorganic
  72272. substrates
  72273. stereoc
  72274. arines
  72275. introduction
  72276. arabinitol
  72277. aracemic
  72278. arachidonic
  72279. araguspongine
  72280. tatsuo
  72281. tokumaru
  72282. katsumi
  72283. photochemical
  72284. adiabatic
  72285. yoshitsugu
  72286. koizumi
  72287. synthesis
  72288. metric
  72289. diels
  72290. arbonyl
  72291. arbonyl
  72292. methylenation
  72293. alkylidenation
  72294. using
  72295. titanium-base
  72296. arborols
  72297. arbuzov
  72298. arbuzov
  72299. boriz
  72300. science
  72301. reviews
  72302. heteroatom
  72303. arcamone
  72304. arcamone
  72305. doxorubicin
  72306. anticancer
  72307. antibiotics
  72308. academic
  72309. press
  72310. archer
  72311. architectural
  72312. flash
  72313. pyrolytic
  72314. reactions
  72315. useful
  72316. nucleophilic
  72317. bimolecular
  72318. concerted
  72319. reactions
  72320. involving
  72321. polar
  72322. organometallic
  72323. compounds
  72324. carbanions
  72325. gegenion
  72326. aregullin
  72327. alkene
  72328. cycloadditions
  72329. organic
  72330. synthesis
  72331. arenarol
  72332. arene
  72333. arene
  72334. diradical
  72335. formation
  72336. dialkynyl
  72337. arenes
  72338. arene
  72339. catalysed
  72340. lithiation
  72341. dichlorobut
  72342. arene
  72343. chromium
  72344. tricarbonyl
  72345. cataly
  72346. reactions
  72347. organic
  72348. arene
  72349. chromium
  72350. tricarbonyl
  72351. stabilized
  72352. benzylic
  72353. carbocations
  72354. arene
  72355. clusters
  72356. arene
  72357. oxides
  72358. shift
  72359. metabolism
  72360. toxicity
  72361. arene
  72362. substitution
  72363. nucleophilic
  72364. addition
  72365. electron
  72366. arene
  72367. syntheses
  72368. extrusion
  72369. heteroatoms
  72370. heterobi
  72371. arene-alkene
  72372. arene-alkene
  72373. photocycloaddition
  72374. reactions
  72375. arene-arene
  72376. arene-arene
  72377. interactions
  72378. electrostatic
  72379. charge-transfer
  72380. arene-chromium
  72381. arene-metal
  72382. arenediazonium
  72383. arenes
  72384. arenesulfonamides
  72385. arenesulfonyl
  72386. arenesulfonyloxy
  72387. arenetellurinic
  72388. arenetellurinic
  72389. anhydrides
  72390. synthetic
  72391. reagents
  72392. arenethiolates
  72393. arenetricarbonylchro
  72394. arenium
  72395. areno
  72396. arenonium
  72397. aresta
  72398. aresta
  72399. michele
  72400. quaranta
  72401. eugenio
  72402. tommasi
  72403. immacolata
  72404. arginine
  72405. ariaans
  72406. aride
  72407. arigoni
  72408. arines
  72409. arising
  72410. arkhipova
  72411. arkhipova
  72412. zhubanov
  72413. rafikov
  72414. heterochain
  72415. polym
  72416. arkles
  72417. arlette
  72418. arlin
  72419. arlin
  72420. lemer
  72421. organic
  72422. reactions
  72423. volume
  72424. review
  72425. jautelat
  72426. lantzsch
  72427. synthesis
  72428. pyrethroid
  72429. acids
  72430. armando
  72431. armarego
  72432. armarego
  72433. quinazolines
  72434. advances
  72435. heterocycli
  72436. armentrout
  72437. armin
  72438. armitage
  72439. armitage
  72440. silicon
  72441. heteroatom
  72442. updates
  72443. armor
  72444. armstrong
  72445. arnaud
  72446. arnaut
  72447. arndt
  72448. arndt
  72449. manganese
  72450. compounds
  72451. oxidizing
  72452. agents
  72453. organic
  72454. arndt-eistert
  72455. arnett
  72456. arnett
  72457. edward
  72458. flowers
  72459. robert
  72460. cleavage
  72461. energies
  72462. arnold
  72463. arnstein
  72464. aroma
  72465. aromas
  72466. aromaticq
  72467. aromatic
  72468. aromatic
  72469. aromatic
  72470. annulation
  72471. strategy
  72472. synthesis
  72473. angularly-
  72474. aromatic
  72475. compounds
  72476. substitution
  72477. cyclisation
  72478. aromatic
  72479. heterocyclic
  72480. chemistry
  72481. aromatic
  72482. organolithium
  72483. reagents
  72484. bearing
  72485. electrophilic
  72486. groups
  72487. aromatic
  72488. quinoid
  72489. systems
  72490. principles
  72491. applications
  72492. aromatic
  72493. substitution
  72494. mechanism
  72495. aromatic
  72496. substitution
  72497. olefins
  72498. palladium
  72499. salts
  72500. aromatic/quinoid
  72501. aromatica
  72502. aromaticityO
  72503. aromatics
  72504. aromatization
  72505. aromatization
  72506. aroney
  72507. arrhizus
  72508. arrow
  72509. arsabenzene
  72510. arsenicN
  72511. arsenic
  72512. compounds
  72513. marine
  72514. organisms
  72515. arsenic-arsenic
  72516. arsenides
  72517. arseniyadis
  72518. arsenor
  72519. arsenyl
  72520. arshinova
  72521. arshinova
  72522. effect
  72523. structure
  72524. organopho
  72525. arsine
  72526. arsinic
  72527. arsinimines
  72528. arsonic
  72529. arsonium
  72530. arsonium
  72531. ylides
  72532. artamkina
  72533. artamkina
  72534. kovalenko
  72535. beletskaya
  72536. reutov
  72537. carbon
  72538. artemisinin
  72539. artemisinin
  72540. qinghaosu
  72541. antimalarial
  72542. arteriosclerosis
  72543. arthur
  72544. arthur
  72545. evaluation
  72546. kinetic
  72547. article
  72548. artifact
  72549. artifcial
  72550. artificial
  72551. artificial
  72552. artificially
  72553. artificially
  72554. elicited
  72555. pabilities
  72556. enzymes
  72557. their
  72558. artur
  72559. arutyunov
  72560. arutyunov
  72561. vedeneev
  72562. pyrolysis
  72563. methane
  72564. tempe
  72565. arvanitis
  72566. aryku
  72567. arylC
  72568. taryl
  72569. alkali
  72570. metal
  72571. compounds
  72572. derivatives
  72573. thallium
  72574. preparation
  72575. hydroperoxides
  72576. alkylaryl
  72577. diaryl
  72578. peroxides
  72579. aryl-aryl
  72580. aryl-substituted
  72581. arylacetates
  72582. arylacetates
  72583. arylacetonitriles
  72584. arylacetylenes
  72585. arylakyl
  72586. arylalkanoic
  72587. arylalkylation
  72588. arylallenes
  72589. arylamines
  72590. arylamino
  72591. arylaminosulfanyl
  72592. arylated
  72593. arylation
  72594. arylation
  72595. urated
  72596. compounds
  72597. diazonium
  72598. salts
  72599. arylation
  72600. reactions
  72601. organobismuth
  72602. reagents
  72603. arylbenzimidoyl
  72604. arylboronate
  72605. arylboronic
  72606. arylcarbenes
  72607. arylchlorocarbenes
  72608. arylcycloalkanes
  72609. arylcyclobutendiones
  72610. arylcyclopropenones
  72611. aryldihydropyridines
  72612. arylene
  72613. arylethanolamines
  72614. arylethers
  72615. arylglycines
  72616. arylhydrazides
  72617. arylhydrazones
  72618. arylhydrazono
  72619. arylic
  72620. arylidene
  72621. aryliodine
  72622. arylketones
  72623. arylmethyl
  72624. arylmethylenefluoren
  72625. arylmethylidenemalon
  72626. arylolefins
  72627. arylolefins
  72628. aryloxy
  72629. aryloxyacetic
  72630. aryloxyl
  72631. aryloyl
  72632. arylperfluoroalkyl
  72633. arylperfluoroalkyl
  72634. arylpolyfluoroalkyli
  72635. salts
  72636. arylpolyfluoroalkyli
  72637. arylpropanoates
  72638. arylpropanoic
  72639. arylpropionic
  72640. arylpyridines
  72641. arylquinolines
  72642. arylseleno
  72643. arylseleno
  72644. chloro
  72645. arylseleno
  72646. cyclopropanes
  72647. arylsulfenium
  72648. arylsulfonyl
  72649. arylsulphonylhydrazo
  72650. aryltellurium
  72651. aryltetrazoles
  72652. arylthio
  72653. arylthioacetamides
  72654. arylthiolation
  72655. arylthionitroso
  72656. arylzinc
  72657. aryne
  72658. arzamastsev
  72659. asami
  72660. asano
  72661. asano
  72662. noble
  72663. activation
  72664. reaction
  72665. volumes
  72666. asato
  72667. ascherl
  72668. ascorbic
  72669. asfari
  72670. asfari
  72671. zouhair
  72672. weiss
  72673. vicens
  72674. jacques
  72675. double
  72676. calixarene
  72677. ashare
  72678. ashby
  72679. group
  72680. heterobenzenes
  72681. 197811
  72682. accounts
  72683. ashit
  72684. ashok
  72685. ashry
  72686. asidospermidine
  72687. asmita
  72688. asmus
  72689. asmus
  72690. stabilization
  72691. oxidized
  72692. sulfur
  72693. centers
  72694. organi
  72695. asokan
  72696. asparagine
  72697. aspartame
  72698. aspartate
  72699. aspartic
  72700. aspect
  72701. aspectsO
  72702. aspects
  72703. aspects
  72704. aromatic
  72705. sandwiches
  72706. application
  72707. organic
  72708. aspergillus
  72709. aspidosperma
  72710. dosperma
  72711. alkaloids
  72712. cyclization
  72713. secodine
  72714. intermedi
  72715. aspidospermidine
  72716. aspinal
  72717. asselineau
  72718. asselineau
  72719. bacterial
  72720. lipids
  72721. containing
  72722. amino
  72723. acids
  72724. assemblage
  72725. assembled
  72726. assemblies
  72727. assembly
  72728. assessment
  72729. assignment
  72730. assignments
  72731. assistance
  72732. assisted
  72733. assisted
  72734. tedcarbonylatio
  72735. associated
  72736. associates
  72737. association
  72738. associations
  72739. asstructural
  72740. asteltoxin
  72741. asteraceae
  72742. astrophysics
  72743. astruc
  72744. astruc
  72745. didier
  72746. transformation
  72747. aromatics
  72748. regio
  72749. astruc
  72750. didier
  72751. transition
  72752. metal
  72753. sandwiches
  72754. reservoirs
  72755. asymetric
  72756. asymm
  72757. asymm
  72758. synthesis
  72759. alpha-amino
  72760. acids
  72761. carbohydrates
  72762. asymmetri
  72763. asymmetricG
  72764. asymmetric
  72765. asymmetric
  72766. asymmetric
  72767. hetero
  72768. diels
  72769. alder
  72770. reactions
  72771. asymmetric
  72772. addition
  72773. organolithium
  72774. reagents
  72775. imines
  72776. asymmetric
  72777. aldol
  72778. reactions
  72779. novel
  72780. model
  72781. switching
  72782. betwe
  72783. asymmetric
  72784. alkenylation
  72785. chiral
  72786. prochiral
  72787. aldehydes
  72788. asymmetric
  72789. alkylation
  72790. allylic
  72791. gem-dicarboxylates
  72792. asymmetric
  72793. selective
  72794. aldol
  72795. reactions
  72796. titanium
  72797. enolat
  72798. asymmetric
  72799. catalyzed
  72800. cycloaddition
  72801. between
  72802. anthrone
  72803. asymmetric
  72804. boron-catalyzed
  72805. reactions
  72806. asymmetric
  72807. carbolithiation
  72808. cinnamyl
  72809. derivatives
  72810. asymmetric
  72811. carbon
  72812. carbon
  72813. formation
  72814. using
  72815. sulfoxide
  72816. asymmetric
  72817. carbon
  72818. carbon
  72819. forming
  72820. reactions
  72821. catalyzed
  72822. asymmetric
  72823. carbon-carbon
  72824. formation
  72825. using
  72826. organometallic
  72827. asymmetric
  72828. carbon-carbon
  72829. formation
  72830. using
  72831. sulfoxide-stab
  72832. asymmetric
  72833. carbon-carbon
  72834. formation
  72835. titanium
  72836. carboh
  72837. asymmetric
  72838. catalysis
  72839. alkaloids
  72840. asymmetric
  72841. catalysis
  72842. chiral
  72843. metal
  72844. complexes
  72845. asymmetric
  72846. catalysis
  72847. carbonyl-ene
  72848. reaction
  72849. asymmetric
  72850. catalysis
  72851. intramolecular
  72852. cyclopropanation
  72853. asymmetric
  72854. catalysis
  72855. organic
  72856. synthesis
  72857. asymmetric
  72858. catalysis
  72859. organic
  72860. synthesis
  72861. industrial
  72862. asymmetric
  72863. catalysis
  72864. diels
  72865. alder
  72866. cycloadditions
  72867. asymmetric
  72868. catalysis
  72869. diels-alder
  72870. cycloadditions
  72871. asymmetric
  72872. catalysis
  72873. hetero
  72874. diels-alder
  72875. cycloadditions
  72876. asymmetric
  72877. catalytic
  72878. aldol
  72879. reaction
  72880. ketene
  72881. silyl
  72882. asymmetric
  72883. catalytic
  72884. aldol
  72885. reaction
  72886. silyl
  72887. ketene
  72888. asymmetric
  72889. catalytic
  72890. hydrogenation
  72891. mechanism
  72892. asymmetric
  72893. catalytic
  72894. hydrogenation
  72895. reactions
  72896. supercritica
  72897. asymmetric
  72898. catalytic
  72899. isomerisation
  72900. functionalised
  72901. olefins
  72902. asymmetric
  72903. catalytic
  72904. synthesis
  72905. b-branched
  72906. aminoacids
  72907. asymmetric
  72908. conjugate
  72909. addition
  72910. asymmetric
  72911. coupling
  72912. reactions
  72913. asymmetric
  72914. creation
  72915. quaternary
  72916. carbon
  72917. centers
  72918. asymmetric
  72919. cycloaddition
  72920. reactions
  72921. asymmetric
  72922. deprotonations
  72923. effic
  72924. enantioselective
  72925. asymmetric
  72926. diels
  72927. alder
  72928. reaction
  72929. design
  72930. chiral
  72931. dienophiles
  72932. asymmetric
  72933. diels
  72934. alder
  72935. reaction
  72936. unsymmetrical
  72937. maleates
  72938. asymmetric
  72939. diels
  72940. alder
  72941. reactions
  72942. chiral
  72943. methacryloylsultam
  72944. asymmetric
  72945. diels-alder
  72946. reactions
  72947. organic
  72948. synthesi
  72949. asymmetric
  72950. diels-alder
  72951. reaction
  72952. unsymetrical
  72953. maleates
  72954. asymmetric
  72955. diels-alder
  72956. reactions
  72957. asymmetric
  72958. diels-alder
  72959. reactions
  72960. chiral
  72961. enoates
  72962. asymmetric
  72963. dihydroxylation
  72964. primary
  72965. allylic
  72966. halides
  72967. asymmetric
  72968. dihydroxylation
  72969. vinyl
  72970. allyl
  72971. silanes
  72972. asymmetric
  72973. electrophilic
  72974. addition
  72975. induction
  72976. asymmetric
  72977. reactions
  72978. ganic
  72979. synthesis
  72980. asymmetric
  72981. epoxidation
  72982. asymmetric
  72983. epoxidation
  72984. allylic
  72985. alcohols
  72986. sharpless
  72987. asymmetric
  72988. selective
  72989. diels
  72990. alder
  72991. reactions
  72992. cyclic
  72993. asymmetric
  72994. exo-selective
  72995. diels-alder
  72996. reaction
  72997. cyclic
  72998. asymmetric
  72999. formation
  73000. quaternary
  73001. centers
  73002. through
  73003. annul
  73004. asymmetric
  73005. formation
  73006. quaternary
  73007. centres
  73008. through
  73009. aza-annul
  73010. asymmetric
  73011. g-methylation
  73012. allylic
  73013. grignard
  73014. reagents
  73015. using
  73016. asymmetric
  73017. hydroarylation
  73018. norbornene
  73019. pheny
  73020. asymmetric
  73021. hetero
  73022. diels
  73023. alder
  73024. reactions
  73025. asymmetric
  73026. hetero-diels-alder
  73027. reactions
  73028. asymmetric
  73029. heterogeneous
  73030. atalytic
  73031. hydrogenation
  73032. asymmetric
  73033. homogeneous
  73034. catalysis
  73035. asymmetric
  73036. homogenous
  73037. hydrogenation
  73038. asymmetric
  73039. hydroboration
  73040. asymmetric
  73041. hydroformylation
  73042. asymmetric
  73043. hydroformylation
  73044. synthesis
  73045. pharmaceutic
  73046. asymmetric
  73047. hydrogen
  73048. transfer
  73049. reactions
  73050. promoted
  73051. homogeneo
  73052. asymmetric
  73053. hydrogenation
  73054. asymmetric
  73055. hydrogenation
  73056. enamines
  73057. chiral
  73058. titanocen
  73059. asymmetric
  73060. hydrogenation
  73061. unfunctionalized
  73062. trisubstituted
  73063. asymmetric
  73064. hydrogenation
  73065. metals
  73066. asymmetric
  73067. hydrosilylation
  73068. hydrocarbonylation
  73069. asymmetric
  73070. hydroxylation
  73071. enolates
  73072. sulfonyloxazirid
  73073. asymmetric
  73074. hydroxylation
  73075. enolates
  73076. n-sulfonyloxazirid
  73077. asymmetric
  73078. induction
  73079. allylic
  73080. alkylations
  73081. acyloxy
  73082. asymmetric
  73083. induction
  73084. intramolecular
  73085. photocycloadditio
  73086. asymmetric
  73087. induction
  73088. radical
  73089. cyclization
  73090. leading
  73091. asymmetric
  73092. induction
  73093. intramolecular
  73094. conjugate
  73095. additio
  73096. asymmetric
  73097. induction
  73098. metal
  73099. promoted
  73100. cycloadditi
  73101. lewis
  73102. dienophile
  73103. complexation
  73104. secondary
  73105. asymmetric
  73106. metal
  73107. carbene
  73108. insertion
  73109. asymmetric
  73110. michael
  73111. additions
  73112. chiral
  73113. unsaturated
  73114. alkox
  73115. asymmetric
  73116. michael
  73117. addition
  73118. lithium
  73119. amides
  73120. aromat
  73121. asymmetric
  73122. michael
  73123. additions
  73124. lithium
  73125. amides
  73126. aroma
  73127. asymmetric
  73128. natural
  73129. product
  73130. synthesis
  73131. asymmetric
  73132. nucleophilic
  73133. addition
  73134. electron
  73135. deficient
  73136. alken
  73137. asymmetric
  73138. olefin
  73139. epoxidation
  73140. sodium
  73141. hypochlorite
  73142. catal
  73143. asymmetric
  73144. hydroxylation
  73145. enolates
  73146. sulfonyloxazirid@
  73147. asymmetric
  73148. induction
  73149. michael
  73150. initiated
  73151. closure
  73152. asymmetric
  73153. oxidation
  73154. esters
  73155. using
  73156. chiral
  73157. cyclic
  73158. asymmetric
  73159. photochemical
  73160. reactions
  73161. solution@
  73162. asymmetric
  73163. closing
  73164. metathesis
  73165. kinetic
  73166. resolution@
  73167. asymmetric
  73168. syntheses
  73169. alpha
  73170. amino
  73171. acids@
  73172. asymmetric
  73173. synthesis
  73174. substituted
  73175. b-amino
  73176. esters@
  73177. asymmetric
  73178. synthesis
  73179. allylsilanes
  73180. palladium
  73181. catalyzed
  73182. thesis
  73183. phleichrome
  73184. audouin@
  73185. auxiliary
  73186. controlled
  73187. 13-dipolar
  73188. cycloadditions
  73189. chiral
  73190. aza-crown
  73191. macrocycles@
  73192. azapurines
  73193. azidonaphthalene
  73194. acylvinyl
  73195. intermolecular
  73196. radical
  73197. additions
  73198. double
  73199. bonds
  73200. lipshutz
  73201. membered
  73202. heteroaromat@
  73203. nagarajan
  73204. suguna
  73205. natarajan
  73206. recent
  73207. b-lithiated@
  73208. bacterial@
  73209. asymmetric
  73210. oxidation
  73211. esters
  73212. using
  73213. chiral
  73214. cyclic
  73215. asymmetric
  73216. pauson-khand
  73217. cyclization
  73218. formal
  73219. total
  73220. synthesis
  73221. tonation
  73222. enolates
  73223. asymmetric
  73224. reactions
  73225. promoted
  73226. titanium
  73227. reagents
  73228. asymmetric
  73229. reduction
  73230. ketoimines
  73231. oxazaborolidine
  73232. asymmetric
  73233. reduction
  73234. chiral
  73235. organoboranes
  73236. based
  73237. asymmetric
  73238. reduction
  73239. organoborane
  73240. reagents
  73241. asymmetric
  73242. reductions
  73243. carbon
  73244. nitrogen
  73245. double
  73246. bonds
  73247. asymmetric
  73248. reductions
  73249. carbon
  73250. nitrogen
  73251. double
  73252. bonds
  73253. asymmetric
  73254. reductions
  73255. carbon-nitrogen
  73256. double
  73257. bonds
  73258. asymmetric
  73259. reductions
  73260. chiral
  73261. complex
  73262. aluminium
  73263. hydrides
  73264. asymmetric
  73265. reductions
  73266. organoborane
  73267. reagents
  73268. asymmetric
  73269. opening
  73270. epoxide
  73271. trimethylsilyl
  73272. azide
  73273. asymmetric
  73274. substitutions
  73275. opposite
  73276. enantioselective
  73277. asymmetric
  73278. syntheses
  73279. methanoamino
  73280. acids
  73281. asymmetric
  73282. syntheses
  73283. 23-methanoamino
  73284. acids
  73285. asymmetric
  73286. syntheses
  73287. alpha
  73288. amino
  73289. acids
  73290. asymmetric
  73291. syntheses
  73292. alpha-amino
  73293. acids
  73294. asymmetric
  73295. syntheses
  73296. chiral
  73297. oxazaborolidines
  73298. asymmetric
  73299. synthesis
  73300. absolute
  73301. configuration
  73302. substitut
  73303. asymmetric
  73304. synthesis
  73305. cram's
  73306. chelate
  73307. asymmetric
  73308. synthesis
  73309. applications
  73310. toward
  73311. synthes
  73312. asymmetric
  73313. synthesis
  73314. reactions
  73315. toluenesulfiny
  73316. asymmetric
  73317. synthesis
  73318. reactions
  73319. p-toluenesulfinyl
  73320. asymmetric
  73321. synthesis
  73322. catalysed
  73323. transition-metal
  73324. complexes
  73325. asymmetric
  73326. synthesis
  73327. construction
  73328. chiral
  73329. molecules
  73330. using
  73331. asymmetric
  73332. synthesis
  73333. asymmetric
  73334. synthesis
  73335. mediated
  73336. chiral
  73337. ligands
  73338. asymmetric
  73339. synthesis
  73340. alkyl
  73341. dihydro
  73342. pyridones
  73343. asymmetric
  73344. synthesis
  73345. substituted
  73346. pyrrolidines
  73347. piper
  73348. asymmetric
  73349. synthesis
  73350. 2-alkyl
  73351. 23-dihydro-4-pyridon
  73352. asymmetric
  73353. synthesis
  73354. hydroxyprolines
  73355. photocyclizatio
  73356. asymmetric
  73357. synthesis
  73358. substituted
  73359. b-amino
  73360. esters
  73361. asymmetric
  73362. synthesis
  73363. a-amino
  73364. acids
  73365. copper
  73366. catalyzed
  73367. asymmetric
  73368. synthesis
  73369. allylic
  73370. sulfones
  73371. useful
  73372. asymmetric
  73373. asymmetric
  73374. synthesis
  73375. amino
  73376. acids
  73377. metalated
  73378. bis-lactim
  73379. asymmetric
  73380. synthesis
  73381. alkyl
  73382. amino
  73383. acids
  73384. asymmetric
  73385. synthesis
  73386. arylglycines
  73387. asymmetric
  73388. synthesis
  73389. aminoacids
  73390. asymmetric
  73391. synthesis
  73392. bioactive
  73393. natural
  73394. relat
  73395. asymmetric
  73396. synthesis
  73397. camptothecin
  73398. alkaloids
  73399. asymmetric
  73400. synthesis
  73401. carbon-carbon
  73402. bonds
  73403. sulfinyl
  73404. asymmetric
  73405. synthesis
  73406. chiral
  73407. macrocyclic
  73408. ligands
  73409. asymmetric
  73410. synthesis
  73411. chiral
  73412. sulfinate
  73413. esters
  73414. sulfoxid
  73415. asymmetric
  73416. synthesis
  73417. dihydro
  73418. pyridones
  73419. addition
  73420. asymmetric
  73421. synthesis
  73422. either
  73423. enantiomer
  73424. opium
  73425. alkaliods
  73426. asymmetric
  73427. synthesis
  73428. erythro
  73429. threo
  73430. a-substituted
  73431. asymmetric
  73432. synthesis
  73433. fluorine
  73434. phosphorus-containin
  73435. asymmetric
  73436. synthesis
  73437. functionalized
  73438. tertiary
  73439. alcohols
  73440. asymmetric
  73441. synthesis
  73442. lignans
  73443. asymmetric
  73444. synthesis
  73445. methylenecyclobutane
  73446. their
  73447. trans
  73448. asymmetric
  73449. synthesis
  73450. natural
  73451. products
  73452. asymmetric
  73453. synthesis
  73454. porantheridine
  73455. asymmetric
  73456. synthesis
  73457. alkyl
  73458. amino
  73459. acids
  73460. asymmetric
  73461. synthesis
  73462. diterpenoid
  73463. marine
  73464. toxin
  73465. acetoxy
  73466. asymmetric
  73467. synthesis
  73468. using
  73469. homochiral
  73470. lithium
  73471. amide
  73472. bases
  73473. asymmetric
  73474. synthesis
  73475. using
  73476. n-sulfonyloxaziridin
  73477. asymmetric
  73478. synthesis
  73479. using
  73480. nucleophilic
  73481. reagents
  73482. containing
  73483. asymmetric
  73484. synthesis
  73485. using
  73486. rganometallic
  73487. catalysts
  73488. asymmetric
  73489. synthesis
  73490. utilizing
  73491. external
  73492. chiral
  73493. ligands
  73494. asymmetric
  73495. synthesis
  73496. chiral
  73497. organoborane
  73498. reagents
  73499. asymmetric
  73500. synthesis
  73501. chiral
  73502. oxazolines
  73503. asymmetric
  73504. synthesis
  73505. norephedrine
  73506. derived
  73507. 2-alkenyloxazo
  73508. asymmetric
  73509. synthesis
  73510. optically
  73511. active
  73512. vinyl
  73513. sulfoxides
  73514. asymmetric
  73515. synthesis
  73516. chiral
  73517. auxiliary
  73518. eta-5-c5h
  73519. asymmetric
  73520. synthesis
  73521. chiral
  73522. hydrogenolysable
  73523. amines
  73524. asymmetric
  73525. synthesis
  73526. chiral
  73527. oxazaborolidines
  73528. asymmetric
  73529. synthesis
  73530. ethers
  73531. asymmetric
  73532. synthesis
  73533. homogeneous
  73534. transition
  73535. asymmetric
  73536. thermal
  73537. reactions
  73538. oppolzer's
  73539. camphor
  73540. sultam
  73541. asymmetric
  73542. total
  73543. synthesis
  73544. asymmetric
  73545. total
  73546. synthesis
  73547. alkaloid
  73548. tacamonine
  73549. radical
  73550. asymmetric
  73551. total
  73552. synthesis
  73553. pancratistatin
  73554. total
  73555. synthesis
  73556. cryptopleurine
  73557. julandi
  73558. asymmetric
  73559. transfer
  73560. hydrogenation
  73561. aromatic
  73562. ketones
  73563. cataly
  73564. asymmetric
  73565. transformations
  73566. catalyzed
  73567. enzymes
  73568. organic
  73569. asymmetric
  73570. transformations
  73571. synthesis
  73572. chiral
  73573. amino
  73574. asymmetric
  73575. trifluoromethylation
  73576. aldehydes
  73577. ketones
  73578. asymmetrically
  73579. asymmetrization
  73580. asymmetrized
  73581. asymmetrized
  73582. methyl
  73583. propanediol
  73584. equivalents
  73585. asymmetrized
  73586. 2-methyl-13-propaned
  73587. equivalents
  73588. prepar
  73589. asymmetry
  73590. asynchronous
  73591. atalytic
  73592. atalyzed
  73593. ateeq
  73594. ateeq
  73595. higher
  73596. order
  73597. cycloaddition
  73598. reactions
  73599. natural
  73600. athanassios
  73601. atharqnthus
  73602. athelstan
  73603. atherton
  73604. atherton
  73605. atherton
  73606. sheppard
  73607. solid
  73608. phase
  73609. peptide
  73610. synthesis
  73611. ating
  73612. ation
  73613. ations
  73614. atkins
  73615. atkinson
  73616. atkinson
  73617. kinetics
  73618. mechanisms
  73619. reactions
  73620. atlas
  73621. atmosphere
  73622. atmospheric
  73623. atom-transfer
  73624. atomic
  73625. atoms
  73626. atrop
  73627. atropdiastereoselect
  73628. atropdiastereoselect
  73629. total
  73630. synthesis
  73631. phleichrome
  73632. atropisomerism
  73633. atroposelective
  73634. atroposelective
  73635. thermal
  73636. reactions
  73637. axially
  73638. twisted
  73639. amides
  73640. atropselective
  73641. atropselective
  73642. thermal
  73643. reactions
  73644. axially
  73645. twisted
  73646. amides
  73647. attaV
  73648. rahman
  73649. choudhary
  73650. recent
  73651. discoveries
  73652. chemi
  73653. rahman
  73654. stereoselective
  73655. synthesis
  73656. studies
  73657. attached
  73658. attachment
  73659. attack
  73660. attanasi
  73661. attempt
  73662. attempted
  73663. attendant
  73664. attraction
  73665. attractive
  73666. attygalle
  73667. atwood
  73668. atwood
  73669. davies
  73670. macnicol
  73671. inclusion
  73672. compounds
  73673. atwood
  73674. jerry
  73675. william
  73676. juneja
  73677. ravindar
  73678. simon
  73679. aubailly
  73680. audouin
  73681. audrey
  73682. augeu
  73683. augustamine
  73684. augustine
  73685. aulbach
  73686. auratus
  73687. aurelia
  73688. aurich
  73689. austalide
  73690. austalides
  73691. austin
  73692. australian
  73693. austria
  73694. autobiographies
  73695. automated
  73696. automated
  73697. synthesis
  73698. structure
  73699. biological
  73700. activity
  73701. automatic
  73702. automation
  73703. automerization
  73704. autooxidation
  73705. autoxidation
  73706. auweraer
  73707. auxihary
  73708. auxilary
  73709. auxiliaries
  73710. auxiliary
  73711. auxiliary
  73712. controlled
  73713. dipolar
  73714. cycloadditions
  73715. chiral
  73716. auxiliary
  73717. controlled
  73718. 13-dipolar
  73719. cycloadditions
  73720. chiral
  73721. auxiliary
  73722. controlled
  73723. selectivity
  73724. cycloaddition
  73725. auxiliary
  73726. mediated
  73727. synthesis
  73728. aziridine
  73729. carboxylic
  73730. available
  73731. avalos
  73732. avalos
  73733. martin
  73734. babiano
  73735. reyes
  73736. cintas
  73737. pedro
  73738. jimenez
  73739. avenaciolide
  73740. avenacolide
  73741. avent
  73742. avent
  73743. birkett
  73744. christides
  73745. crane
  73746. darwish
  73747. averina
  73748. avermectins
  73749. avermectins
  73750. milbemycins
  73751. avermectins
  73752. milbemycins
  73753. avermectins
  73754. milbemycins
  73755. avertsev
  73756. avetisyan
  73757. avetisyan
  73758. dangyan
  73759. chemistry
  73760. butenolides
  73761. avila
  73762. avotins
  73763. avotins
  73764. aminoacids
  73765. cyclobutane
  73766. series
  73767. russian
  73768. chemi
  73769. avramovic
  73770. awadi
  73771. awamycin
  73772. award
  73773. axelson
  73774. axially
  73775. ayalon
  73776. browne
  73777. terpenoid
  73778. metabolites
  73779. mushrooms
  73780. lycopodium
  73781. alkaloids
  73782. natural
  73783. product
  73784. reports
  73785. willima
  73786. trifonov
  73787. latchezar
  73788. licopodium
  73789. alkaloids
  73790. ayers
  73791. ayhan
  73792. ayman
  73793. ayyangar
  73794. ayyangar
  73795. lugade
  73796. naphthindolizine
  73797. naphthimidazopy
  73798. wittig
  73799. rearrangement
  73800. vinylaziridenes
  73801. analogs
  73802. organic
  73803. inorganic
  73804. oxygen
  73805. compounds
  73806. claisen
  73807. rearrangements
  73808. initiated
  73809. catalyzed
  73810. micha
  73811. payne
  73812. rearrangement
  73813. activated
  73814. 2-aziridine
  73815. methanols
  73816. aza-annulation
  73817. aza-arenes
  73818. aza-crown
  73819. aza-crown
  73820. macrocycles
  73821. aza-wittig
  73822. azaacetals
  73823. azaadamantanes
  73824. azaadamantanes
  73825. trogen
  73826. atoms
  73827. bridgehead
  73828. positio
  73829. azaallyl
  73830. azaaromatic
  73831. azaaromatics
  73832. azaazulenes
  73833. azabicyclo
  73834. azabicyclooctadienes
  73835. azabutadienes
  73836. azacoumestans
  73837. azacrown
  73838. azacycl
  73839. azadienes
  73840. azadiindoles
  73841. azadirachtin
  73842. azafluoranthene
  73843. azafulvenium
  73844. azaheterocycles
  73845. azaindole
  73846. azaindoles
  73847. azaindolium
  73848. azaindolizine
  73849. azaindolyl
  73850. azalactones
  73851. azamacrocycles
  73852. azamodified
  73853. azanonatrienes
  73854. azanucleosides
  73855. azaparacyclophanes
  73856. azapentalenes
  73857. azapeptides
  73858. azaphenalenes
  73859. azaphenothiazines
  73860. azaphosphorines
  73861. azaphosphorins
  73862. azaporphin
  73863. azapurines
  73864. azapurines
  73865. azapyrylium
  73866. azaspiro
  73867. azasugars
  73868. azenes
  73869. azepin
  73870. azepine
  73871. azepines
  73872. azetes
  73873. azetidine
  73874. azetidine
  73875. pyrrole
  73876. pyrrolidine
  73877. piperidine
  73878. pyridine
  73879. alkalo
  73880. azetidines
  73881. azetidines
  73882. 34-dihydroazetidines
  73883. 14-dihydroazetes
  73884. azetes
  73885. azetidines
  73886. azetines
  73887. azetidinone
  73888. azetidinones
  73889. azetidinyl
  73890. azetines
  73891. azicao
  73892. azide
  73893. azide-diene
  73894. azides
  73895. synthetic
  73896. azido
  73897. azidobenzonitriles
  73898. azidoformate
  73899. azidohydrazones
  73900. azidoiodinanes
  73901. azidomethyl
  73902. azidonaphthalene
  73903. azidonaphthalene
  73904. azidonation
  73905. azidosilanes
  73906. azidotrimethylsilane
  73907. azimine
  73908. azine
  73909. azines
  73910. azines
  73911. imines
  73912. pyrrole
  73913. aldehyde
  73914. azinohydrazone
  73915. azinyl
  73916. azinyl-azinylid
  73917. azinylidene
  73918. azinylmethanes
  73919. aziridination
  73920. aziridine
  73921. aziridines
  73922. dines
  73923. azirines
  73924. fused-ring
  73925. derivatives
  73926. aziridinyl
  73927. azirine
  73928. azirines
  73929. azirino
  73930. azlactones
  73931. azlactones
  73932. carter
  73933. organic
  73934. reactions
  73935. volume
  73936. azlactones
  73937. retrospect
  73938. prospect
  73939. aznar
  73940. compounds
  73941. diazenes
  73942. azoalkanes
  73943. azoalkenes
  73944. azobenzene
  73945. azocines
  73946. azodicarbonyl
  73947. azodicarboxylate
  73948. azodicarboxylates
  73949. azoisobutyronitrile
  73950. azole
  73951. azoles
  73952. azolones
  73953. azolylmethyl
  73954. azomethide
  73955. azomethine
  73956. ylide
  73957. cycloadditions
  73958. 12-prototropy
  73959. metall
  73960. azomethine
  73961. ylids
  73962. azomethine
  73963. imines
  73964. iminophosphoranes
  73965. azomethines
  73966. azoniaallene
  73967. azoxy
  73968. azoxy
  73969. compounds
  73970. diazene
  73971. 1-oxide
  73972. azulene
  73973. azulenes
  73974. azulenoid
  73975. superbasic
  73976. acylvinyl
  73977. intermolecular
  73978. radical
  73979. additions
  73980. double
  73981. bonds
  73982. acylvinyl
  73983. intermolecular
  73984. radical
  73985. additions
  73986. double
  73987. bonds
  73988. bogdanovic
  73989. angew
  73990. catalytic
  73991. bogdanovic
  73992. angew
  73993. catalytic
  73994. synthes
  73995. weedon
  73996. synthesis
  73997. capon
  73998. mechanistic
  73999. studies
  74000. hydrolysis
  74001. acetals
  74002. coxon
  74003. nitrogen
  74004. studies
  74005. amino
  74006. sugars
  74007. dynamic
  74008. spectroscopy
  74009. progress
  74010. maryanoff
  74011. stereoch
  74012. epoxysilanes
  74013. fraser
  74014. progeny
  74015. functionalised
  74016. radicals
  74017. organic
  74018. synthesis
  74019. acyloxyalky
  74020. ganem
  74021. synthetically
  74022. giese
  74023. angew
  74024. syntheses
  74025. giese
  74026. basis
  74027. limitations
  74028. reactivity
  74029. selectivity
  74030. giese
  74031. tetrahedron
  74032. selectivity
  74033. synthetic
  74034. lipshutz
  74035. membered
  74036. heteroaromat
  74037. halton
  74038. stang
  74039. alkylidenecy
  74040. iddon
  74041. heterocycles
  74042. metallation
  74043. metal
  74044. halog
  74045. hudson
  74046. immobilized
  74047. enzymes
  74048. mcardle
  74049. sherwood
  74050. london
  74051. lindberg
  74052. structural
  74053. studies
  74054. bacterial
  74055. polysacchari
  74056. dilworth
  74057. mckervey
  74058. tetrahedron
  74059. organ
  74060. mikhailov
  74061. methods
  74062. synthesis
  74063. trost
  74064. angew
  74065. cycloaddition
  74066. trost
  74067. angew
  74068. cycloaddition
  74069. trost
  74070. organomet
  74071. transition
  74072. metals
  74073. trost
  74074. organopalladium
  74075. intermediates
  74076. organic
  74077. synthesis
  74078. trost
  74079. science
  74080. sculpting
  74081. horizons
  74082. organic
  74083. diazo
  74084. carbonyl
  74085. compounds
  74086. conversion
  74087. chiral
  74088. mundy
  74089. lipkowitz
  74090. dirks
  74091. chemistry
  74092. nagarajan
  74093. suguna
  74094. natarajan
  74095. recent
  74096. stannyl
  74097. allylic
  74098. alcohols
  74099. through
  74100. photooxygenation
  74101. schenck
  74102. synthesis
  74103. segment
  74104. rutamycin
  74105. brobel
  74106. seebach
  74107. polarization
  74108. reversal
  74109. reactivity
  74110. trofimov
  74111. intermediates
  74112. organic
  74113. rockett
  74114. organomet
  74115. revie
  74116. b-acyl
  74117. b-acyl
  74118. vinyl
  74119. anion
  74120. equivalents
  74121. b-lithiated
  74122. unsaturated
  74123. b-alkoxy
  74124. b-alkyl-9-borabicycl
  74125. b-alkylketo
  74126. b-amyrin
  74127. b-benzyloxy
  74128. b-bis
  74129. b-branched
  74130. b-c-trehaloses
  74131. b-containing
  74132. b-copper
  74133. b-copper
  74134. ketones
  74135. generation
  74136. coupling
  74137. highly
  74138. stereosel
  74139. b-enamino
  74140. b-epoxy
  74141. b-fluorovinamidinium
  74142. b-fragmentation-cycl
  74143. b-heteroatom
  74144. b-hyroxyl
  74145. b-keto
  74146. b-ketoethynyl
  74147. b-lactam
  74148. b-lactams
  74149. b-lithiated
  74150. b-mannopyranosides
  74151. b-nitrogen
  74152. b-oxoaldiminato
  74153. b-phenylsulfonyl
  74154. b-phosphinocarboxyli
  74155. b-selective
  74156. b-substituent
  74157. b-unsatutated
  74158. b/c/d
  74159. babak
  74160. babiano
  74161. babichev
  74162. balasubramaniam
  74163. simple
  74164. facile
  74165. oxidation
  74166. ramesh
  74167. ramana
  74168. ramadas
  74169. synthesis
  74170. condensed
  74171. baccatin
  74172. catalytic
  74173. enantioselective
  74174. coupling
  74175. allyl
  74176. transfe
  74177. bachi
  74178. bachi
  74179. mario
  74180. balanov
  74181. bosch
  74182. denenmark
  74183. bachmann
  74184. bachowska
  74185. baciocchi
  74186. baciocchi
  74187. dependence
  74188. transition
  74189. state
  74190. structure
  74191. backbone
  74192. backbone-modified
  74193. backbones
  74194. backdonation
  74195. backlund
  74196. backvall
  74197. backvall
  74198. palladium
  74199. catalyzed
  74200. intramolecular
  74201. additio
  74202. bacterial
  74203. bacterial
  74204. lipids
  74205. containing
  74206. amino
  74207. acids
  74208. peptides
  74209. linked
  74210. badanyan
  74211. bader
  74212. bader
  74213. richard
  74214. quantum
  74215. theory
  74216. molecular
  74217. structure
  74218. bador
  74219. bador
  74220. pascal
  74221. surrel
  74222. marie
  74223. noelle
  74224. computer
  74225. systems
  74226. search
  74227. baeckvsll
  74228. baerheim
  74229. baeyer
  74230. baeyer-villiger
  74231. bafilomycin
  74232. baggott
  74233. baghurst
  74234. bagrii
  74235. bahman
  74236. bahrman
  74237. bahrman
  74238. cornils
  74239. homologation
  74240. alcohols
  74241. syntheses
  74242. bahrmann
  74243. bahrmann
  74244. reactions
  74245. syntheses
  74246. carbon
  74247. monoxide
  74248. bailery
  74249. bailey
  74250. bailey
  74251. introduction
  74252. peptide
  74253. chemistry
  74254. wiley
  74255. chiche
  74256. bailey
  74257. ozonation
  74258. organic
  74259. chemistry
  74260. academic
  74261. press
  74262. bailey
  74263. ozonation
  74264. organic
  74265. chemistry
  74266. academic
  74267. bailey
  74268. william
  74269. ovaska
  74270. generation
  74271. cyclization
  74272. bailey
  74273. william
  74274. ovaska
  74275. generation
  74276. cyclization
  74277. baines
  74278. baiocchi
  74279. baiocchi
  74280. corsi
  74281. palazzo
  74282. synthesis
  74283. properties
  74284. reaction
  74285. baird
  74286. baird
  74287. dihalocyclopropenes
  74288. chemical
  74289. baiyunoside
  74290. baizer
  74291. baker
  74292. baker
  74293. russell
  74294. biosynthesis
  74295. marine
  74296. sterols
  74297. baker
  74298. gregory
  74299. young
  74300. james
  74301. systematic
  74302. nomenclature
  74303. baker
  74304. murphy
  74305. compounds
  74306. marine
  74307. organisms
  74308. baker
  74309. murphy
  74310. compounds
  74311. marine
  74312. organisms
  74313. baker
  74314. carbon
  74315. carbon
  74316. forming
  74317. reactions
  74318. allyl
  74319. comple
  74320. baker's
  74321. baker's
  74322. yeast
  74323. mediated
  74324. transformations
  74325. organic
  74326. chemistry
  74327. bakers
  74328. bakers
  74329. yeast
  74330. reagent
  74331. organic
  74332. synthesis
  74333. bakhmutov
  74334. bakker
  74335. bakuchiol
  74336. bakulev
  74337. balaban
  74338. bailey
  74339. william
  74340. ovaska
  74341. generation
  74342. cyclization
  74343. balaban
  74344. pyrylium
  74345. cation
  74346. synthon
  74347. organic
  74348. chem@
  74349. balzani@
  74350. barabanov
  74351. barluenga
  74352. joglar
  74353. gonzalez
  74354. fustero
  74355. electronically
  74356. bartlett
  74357. stereocontrol
  74358. synthesis
  74359. acyclic
  74360. syste@
  74361. dependence
  74362. transition-state
  74363. structure
  74364. alkene-form@
  74365. beckmann
  74366. rearrangements/allyl
  74367. cyclizations
  74368. approach
  74369. behrens
  74370. decades
  74371. metal
  74372. carbonyl
  74373. chemistry
  74374. liquid@
  74375. belokon
  74376. chiral
  74377. complexes
  74378. nickel
  74379. copper
  74380. bennett
  74381. benzazepinediones
  74382. benzimidazoles
  74383. benzodiazepines
  74384. benzothiazepines@
  74385. benzoylimidazoles@
  74386. berger
  74387. nuclear
  74388. magnetic
  74389. relaxation
  74390. recent
  74391. problems
  74392. bernasconi
  74393. claude
  74394. principle
  74395. perfect
  74396. synchroniza@
  74397. beschke
  74398. reactions
  74399. cycloalkenopyridines
  74400. betain@
  74401. betweenanenes@
  74402. bhatia
  74403. balaban
  74404. pyrylium
  74405. cation
  74406. synthon
  74407. organic
  74408. balaban
  74409. alexandru
  74410. benzenoid
  74411. catafusenes
  74412. perfect
  74413. matchings
  74414. balancing
  74415. balancing
  74416. leaving
  74417. group
  74418. ability
  74419. effect
  74420. exploring
  74421. balanol
  74422. balanov
  74423. balasubramaniam
  74424. balasubramanian
  74425. balasubramanian
  74426. scriven
  74427. shobana
  74428. approache
  74429. balasuframanian
  74430. balch
  74431. balci
  74432. balci
  74433. bicyclic
  74434. endoperoxides
  74435. synthetic
  74436. appli
  74437. cations
  74438. baldomero
  74439. baldwin
  74440. baldwin
  74441. aldous
  74442. harwood
  74443. o'neil
  74444. peach
  74445. baldwin
  74446. synthetic
  74447. aspects
  74448. cycloadditions
  74449. baldwin's
  74450. balen
  74451. balitsky
  74452. ballah
  74453. ballester
  74454. ballini
  74455. balls
  74456. bally
  74457. bally
  74458. masamune
  74459. cyclobutadiene
  74460. tetrahedron
  74461. balogh
  74462. balogh
  74463. laszlo
  74464. organic
  74465. chemistry
  74466. using
  74467. clays
  74468. springer
  74469. balyeva
  74470. balzani
  74471. balzani
  74472. vincenzo
  74473. scandola
  74474. franco
  74475. supramolecular
  74476. photochemist
  74477. balzani
  74478. vincenzo
  74479. supramolecular
  74480. photochemistry
  74481. bamezai
  74482. bamrung
  74483. banaszczyk
  74484. banaszek
  74485. bandini
  74486. bando
  74487. bandyopadhyay
  74488. banerjee
  74489. banerjee
  74490. kumar
  74491. gonzalez
  74492. nieves
  74493. canudas
  74494. methods
  74495. banerjee
  74496. kumar
  74497. gonzalez
  74498. nieves
  74499. canudas
  74500. methods
  74501. banfi
  74502. banfi
  74503. guanti
  74504. giuseppe
  74505. asymmetrized
  74506. methyl
  74507. propaned
  74508. banister
  74509. banister
  74510. rawson
  74511. dithiadiazoles
  74512. family
  74513. effects
  74514. steric
  74515. strain
  74516. preparation
  74517. stability
  74518. banks
  74519. bannemann
  74520. banoub
  74521. banoub
  74522. joseph
  74523. boullanger
  74524. lafont
  74525. dominique
  74526. synthesis
  74527. banwell
  74528. banwell
  74529. martin
  74530. methods
  74531. synthesis
  74532. troponoid
  74533. banwell
  74534. martin
  74535. monica
  74536. dihalocyclopropanes
  74537. barabanov
  74538. barabanov
  74539. barabanov
  74540. golovin
  74541. rodin
  74542. ustenko
  74543. electron
  74544. baraldi
  74545. baran
  74546. baraniak
  74547. baraniak
  74548. janina
  74549. wojciech
  74550. stereocontrolled
  74551. syntheses
  74552. baranov
  74553. baranov
  74554. perekalin
  74555. aliphatic
  74556. organophosphorus
  74557. nitro
  74558. baranovskii
  74559. baranovskii
  74560. litvinovskaya
  74561. khripach
  74562. steroids
  74563. baranowski
  74564. barany
  74565. barany
  74566. merrifield
  74567. solid
  74568. phase
  74569. peptide
  74570. synthesis
  74571. barashkov
  74572. barashkov
  74573. sakhno
  74574. nurmukhametov
  74575. khakhel
  74576. excim
  74577. barauskaite
  74578. barbachyn
  74579. barbara
  74580. barbas
  74581. barber
  74582. barbi
  74583. barbier
  74584. barco
  74585. bardin
  74586. baretta
  74587. barium
  74588. barkash
  74589. barker
  74590. barker
  74591. rosenfarb
  74592. caruso
  74593. ureas
  74594. solvents
  74595. barkhash
  74596. barlin
  74597. barluenga
  74598. barluenga
  74599. joglar
  74600. gonzalez
  74601. fustero
  74602. electronically
  74603. barna
  74604. barnett
  74605. barnette
  74606. barney
  74607. barnikow
  74608. barone
  74609. barone
  74610. chanon
  74611. synthesis
  74612. ellipticine
  74613. review
  74614. comput
  74615. barot
  74616. barrau
  74617. barreto
  74618. barrett
  74619. barrett
  74620. anthony
  74621. heterosubstituted
  74622. nitroalkenes
  74623. synthe
  74624. barrett
  74625. anthony
  74626. jason
  74627. wallace
  74628. flygare
  74629. barrett
  74630. chemistry
  74631. thiazolinone
  74632. hydroxy
  74633. barretta
  74634. barrier
  74635. barriers
  74636. barron
  74637. barron
  74638. andrew
  74639. reactions
  74640. group
  74641. alkyls
  74642. dioxygen
  74643. barrow
  74644. barry
  74645. barry
  74646. bates
  74647. robert
  74648. beavers
  74649. wiiliam
  74650. camou
  74651. barry
  74652. bates
  74653. robert
  74654. beavers
  74655. william
  74656. camou
  74657. barth
  74658. barth
  74659. djerassi
  74660. circular
  74661. dichroism
  74662. molecules
  74663. bartlett
  74664. bartlett
  74665. stereocontrol
  74666. synthesis
  74667. acyclic
  74668. syste
  74669. bartlett
  74670. landis
  74671. dioxetanes
  74672. singlet
  74673. oxygen
  74674. bartmann
  74675. bartoli
  74676. barton
  74677. barton
  74678. invention
  74679. chemical
  74680. reactions
  74681. relevanc
  74682. barton
  74683. invention
  74684. chemical
  74685. reactions
  74686. barton
  74687. derek
  74688. doller
  74689. dario
  74690. selective
  74691. functionalizatio
  74692. barton
  74693. derek
  74694. century
  74695. radical
  74696. chemistry
  74697. barton
  74698. derek
  74699. parekh
  74700. shyamal
  74701. ligand
  74702. coupling
  74703. based
  74704. barton
  74705. derek
  74706. recollections
  74707. jumpmg
  74708. profil
  74709. barton
  74710. benzo
  74711. cinnolines
  74712. advances
  74713. hetero
  74714. bartsch
  74715. bartsch
  74716. zavada
  74717. stereochemical
  74718. species
  74719. dichoto
  74720. basavaU
  74721. basava
  74722. anantharamaiah
  74723. peptides
  74724. design
  74725. synthesis
  74726. basavaiah
  74727. basavaiah
  74728. deevi
  74729. krishna
  74730. peddinti
  74731. enantioselective
  74732. synth
  74733. baschang
  74734. dependence
  74735. transition-state
  74736. structure
  74737. alkene-form
  74738. base-catalysed
  74739. base-catalysed
  74740. addition
  74741. reactions
  74742. hydrocarbons
  74743. base-catalysed
  74744. isomerisations
  74745. acetylenes
  74746. base-initiated
  74747. base-promoted
  74748. base-promoted
  74749. imine-forming
  74750. 12-elimination
  74751. tions
  74752. base-promoted
  74753. isomerisations
  74754. epoxides
  74755. base-sensitive
  74756. based
  74757. based
  74758. bases
  74759. basha
  74760. bashir
  74761. basicE
  74762. basic
  74763. principles
  74764. carbene
  74765. chemistry
  74766. applications
  74767. basicities
  74768. basicity
  74769. basics
  74770. basidiomycetes
  74771. basil
  74772. basilevskii
  74773. basilevskii
  74774. faustov
  74775. modern
  74776. theories
  74777. chemical
  74778. basis
  74779. basis
  74780. basis
  74781. limitations
  74782. reactivity-selectivi
  74783. principle
  74784. baskets
  74785. basolo
  74786. bassindale
  74787. bassler
  74788. bassner
  74789. bastock
  74790. bastos
  74791. batcheller
  74792. batcho
  74793. bates
  74794. bates
  74795. dianions
  74796. polyanions
  74797. comprehensive
  74798. carbanion
  74799. batesonT
  74800. bateson
  74801. mitchell
  74802. organometallic
  74803. reagents
  74804. orgaT
  74805. battelle
  74806. battered
  74807. battered
  74808. benzene
  74809. twisted
  74810. ethene
  74811. battersby
  74812. battersby
  74813. nature
  74814. builds
  74815. pigments
  74816. battersby
  74817. mcdonald
  74818. problem
  74819. porphyrin
  74820. battle
  74821. batyeva
  74822. baudin
  74823. baudler
  74824. baudler
  74825. marianne
  74826. glinka
  74827. klaus
  74828. contributions
  74829. chemistry
  74830. bauer
  74831. bauer
  74832. walter
  74833. schleyer
  74834. rague
  74835. recent
  74836. results
  74837. bauld
  74838. bauman
  74839. baumann
  74840. baumann
  74841. baumann
  74842. wolfram
  74843. zsolt
  74844. photoinduced
  74845. charge
  74846. transfer
  74847. baumgarten
  74848. baumgarten
  74849. martin
  74850. mullen
  74851. klaus
  74852. radical
  74853. where
  74854. organic
  74855. baumgartner
  74856. baumstark
  74857. baumstark
  74858. boykin
  74859. spectroscopy
  74860. applications
  74861. baxter
  74862. bayer
  74863. bayer
  74864. ernst
  74865. toward
  74866. chemical
  74867. synthesis
  74868. proteins
  74869. bazin
  74870. beach
  74871. beacham
  74872. reitz
  74873. dipole
  74874. stabilized
  74875. carbanions
  74876. novel
  74877. peter
  74878. determinations
  74879. transition
  74880. state
  74881. geometries
  74882. beale
  74883. beale
  74884. biosynthesis
  74885. terpenoid
  74886. compounds
  74887. natural
  74888. bearing
  74889. beaucage
  74890. beaucage
  74891. serge
  74892. radhakrishnan
  74893. advances
  74894. synthe
  74895. beaucage
  74896. serge
  74897. radhakrishnan
  74898. functionalization
  74899. beaucage
  74900. serge
  74901. radhakrishnan
  74902. synthesis
  74903. modif
  74904. beaucage
  74905. serge
  74906. radhakrishnan
  74907. synthesis
  74908. speci
  74909. beauchamp
  74910. beautiful
  74911. beavan
  74912. beavan
  74913. photoluminescence
  74914. methods
  74915. polymer
  74916. scienc
  74917. beavers
  74918. bechamp
  74919. becher
  74920. becher
  74921. synthesis
  74922. reactions
  74923. glutaconaldehyde
  74924. bechyne
  74925. nucleophilic
  74926. displacement
  74927. aromatic
  74928. nitro
  74929. groups
  74930. becker
  74931. becker
  74932. dieter
  74933. unimolecular
  74934. photochemistry
  74935. anthracene
  74936. becker
  74937. cycloalkenes
  74938. intramolecular
  74939. wittig
  74940. reaction
  74941. beckhaus
  74942. beckmann
  74943. beckmann
  74944. rearrangement
  74945. allylsilane
  74946. cyclizations
  74947. approach
  74948. beckmann
  74949. rearrangements/allyl
  74950. cyclizations
  74951. approach
  74952. beckwith
  74953. beckwith
  74954. ingold
  74955. radical
  74956. rearrangements
  74957. rearra
  74958. beckwith
  74959. regioselectivity
  74960. stereoselectivity
  74961. beckwith
  74962. athelstan
  74963. pursuit
  74964. selectivity
  74965. radical
  74966. bedeschi
  74967. bednarski
  74968. bednyagina
  74969. beena
  74970. beerli
  74971. beets
  74972. before
  74973. begtrup
  74974. begtrup
  74975. mikael
  74976. general
  74977. description
  74978. reactivity
  74979. begue
  74980. begue
  74981. charpentier
  74982. morize
  74983. acylcarbenium
  74984. begue
  74985. pierre
  74986. bonnet
  74987. delpon
  74988. daniele
  74989. preparation
  74990. trifl
  74991. behavior
  74992. behavior
  74993. monocyclic
  74994. 124-triazines
  74995. reactions
  74996. behaviors
  74997. behaviour
  74998. behrens
  74999. behrens
  75000. decades
  75001. metal
  75002. carbonyl
  75003. chemistry
  75004. liquid
  75005. beifuss
  75006. beirut
  75007. bekkum
  75008. bel'skii
  75009. bel'skii
  75010. polikarpov
  75011. kabachnik
  75012. cyclopendant
  75013. bel'skii
  75014. kinetics
  75015. hydrolysis
  75016. phosphate
  75017. esters
  75018. belder
  75019. belen'kii
  75020. belen'kii
  75021. relative
  75022. stabilities
  75023. hetarenium
  75024. factor
  75025. belen'kii
  75026. vol'kenshtein
  75027. karmanova
  75028. beletskaya
  75029. beletskaya
  75030. drozd
  75031. mechanism
  75032. nucleophilic
  75033. belevskii
  75034. belikov
  75035. belin
  75036. belkin
  75037. belkin
  75038. polezhaeva
  75039. chemistry
  75040. stabilized
  75041. sulfo
  75042. bellama
  75043. bellur
  75044. bellus
  75045. bellus
  75046. physical
  75047. quenchers
  75048. singlet
  75049. molecular
  75050. oxygen
  75051. bellus
  75052. syntheses
  75053. highly
  75054. oxidized
  75055. cyclobutanes
  75056. beloglazkina
  75057. belokon
  75058. belokon
  75059. chiral
  75060. complexes
  75061. nickel
  75062. copper
  75063. belomycin
  75064. belov
  75065. belov
  75066. chiral
  75067. mobile
  75068. phases
  75069. enantiomeric
  75070. analys
  75071. below
  75072. belshaw
  75073. meyer
  75074. johnson
  75075. ikeda
  75076. andrus
  75077. belson
  75078. belts
  75079. bemiller
  75080. bemiller
  75081. james
  75082. whistler
  75083. derik
  75084. lipopolysac
  75085. quinolizinium
  75086. salts
  75087. bender
  75088. bender
  75089. komiyama
  75090. cyclodextrin
  75091. chemistry
  75092. springer
  75093. verlag
  75094. benedetti
  75095. benedict
  75096. benedicte
  75097. beneficial
  75098. bengt
  75099. benjamin
  75100. benjamin/cummings
  75101. benjamina
  75102. benjes
  75103. benjes
  75104. grimmett
  75105. alkylation
  75106. nitrogen
  75107. azole
  75108. benkovic
  75109. bennasar
  75110. benneche
  75111. benner
  75112. benner
  75113. ellington
  75114. evolution
  75115. structural
  75116. theory
  75117. bennetau
  75118. bennetau
  75119. bernard
  75120. dunogues
  75121. jacques
  75122. unusual
  75123. electrophilic
  75124. bennett
  75125. bennett
  75126. benninga
  75127. benoit
  75128. benoiton
  75129. benoiton
  75130. omega
  75131. alkyldiamino
  75132. acids
  75133. chemistry
  75134. proper
  75135. benson
  75136. benson
  75137. spillane
  75138. sulfamic
  75139. substituted
  75140. benson
  75141. nangia
  75142. problems
  75143. oxidation
  75144. combustion
  75145. benson
  75146. thermochemistry
  75147. kinetics
  75148. sulfur
  75149. containing
  75150. bentley
  75151. bentley
  75152. phenylethylamines
  75153. isoquinoline
  75154. bentrude
  75155. benvalene
  75156. benvalene
  75157. properties
  75158. synthetic
  75159. potential
  75160. herbert
  75161. solid
  75162. phase
  75163. fragment
  75164. condensation
  75165. benzaldehyde
  75166. ldehydes
  75167. benzannelated
  75168. benzannelated
  75169. cycloboranes
  75170. benzannelation
  75171. benzannulation
  75172. benzannulation
  75173. podocarpic
  75174. derivatives
  75175. directed
  75176. benzannulenes
  75177. benzazepinediones
  75178. benzazepinediones
  75179. benzazepinediones
  75180. reaction
  75181. anthranilides
  75182. under
  75183. benzazepinium
  75184. benzazetes
  75185. benzene
  75186. benzene
  75187. derivatives
  75188. bridging
  75189. ligands
  75190. transitio
  75191. benzenes
  75192. benzenesulfenyl
  75193. benzenesulfonyl
  75194. benzenetellurolate
  75195. benzenethiol
  75196. benzenoid
  75197. benzenoid
  75198. polycyclic
  75199. aromatic
  75200. natural
  75201. products
  75202. benzenoid
  75203. catafusenes
  75204. perfect
  75205. matchings
  75206. isomerization
  75207. autome
  75208. benzenoid
  75209. chemical
  75210. isomers
  75211. their
  75212. enumeration
  75213. benzenoids
  75214. benzidine
  75215. benzil
  75216. benzil-benzilic
  75217. benzil-benzilic
  75218. rearrangements
  75219. benzimidazole
  75220. benzimidazoles
  75221. benzimidazoles
  75222. benzo
  75223. benzo
  75224. furans
  75225. 2-benzofurans
  75226. benzo
  75227. pyrilium
  75228. syntheses
  75229. reactions
  75230. physical
  75231. prope
  75232. benzo
  75233. quinolizinium
  75234. salts
  75235. benzoannulation
  75236. benzoate
  75237. benzocrown
  75238. benzocyclobutadiene
  75239. benzocyclobutene
  75240. benzocyclobutene
  75241. derivatives
  75242. benzocyclobutene
  75243. related
  75244. compounds
  75245. benzocyclobutenes
  75246. benzocyclobutenes
  75247. related
  75248. compounds
  75249. benzocyclobutenone
  75250. benzocyclobutenoxide
  75251. benzocyclopropanes
  75252. benzocyclopropenes
  75253. benzodiazepine
  75254. benzodiazepine
  75255. alkaloids
  75256. benzodiazepines
  75257. benzodiazepines
  75258. benzodiazepines
  75259. handbook
  75260. benzodiazocines
  75261. benzodicyclobutadien
  75262. benzodioxane
  75263. benzodipyrazoles
  75264. benzodithiastannoles
  75265. benzodithiins
  75266. benzofuran
  75267. benzofuranosesquiter
  75268. benzofurans
  75269. benzofuranylacetate
  75270. benzofurazanes
  75271. benzofuroxans
  75272. benzoin
  75273. benzoins
  75274. benzolactams
  75275. benzologs
  75276. benzomorphans
  75277. benzopentalene
  75278. benzopentathiepin
  75279. benzophenanthridine
  75280. benzophenones
  75281. benzopyran
  75282. benzopyran-4-ones
  75283. benzopyran-4-ones
  75284. containing
  75285. 23-fused
  75286. heterocyclic
  75287. benzopyranobenazepin
  75288. benzopyranopyrazole
  75289. benzopyrans
  75290. benzopyrazoles
  75291. benzoquinazolines
  75292. benzoquinone
  75293. benzoquinoneimines
  75294. benzoquinones
  75295. benzothiazepine
  75296. benzothiazepines
  75297. benzothiazines
  75298. benzothiazinone
  75299. benzothiazol
  75300. benzothiazole
  75301. benzothiepins
  75302. benzothiophenium
  75303. benzotriazepines
  75304. benzotriazol
  75305. benzotriazole
  75306. benzotriazole
  75307. novel
  75308. synthetic
  75309. auxiliary
  75310. benzotriazole
  75311. synthetic
  75312. auxiliary
  75313. benzotriazolyl
  75314. alkyla
  75315. benzotriazole
  75316. synthetic
  75317. auxiliary
  75318. benzotriazolylalkyla
  75319. benzotriazole
  75320. assisted
  75321. lithiation
  75322. vinyl
  75323. ethers
  75324. benzotriazole
  75325. mediated
  75326. synthesis
  75327. trisubstitute
  75328. benzotriazole-mediat
  75329. benzotriazole-mediat
  75330. arylalkylation
  75331. heteroarylalkylation
  75332. benzotriazoles
  75333. benzotriazolyl
  75334. benzotriazolylalkyla
  75335. benzotrithiole
  75336. benzotrithioles
  75337. benzoxazepines
  75338. benzoxazine
  75339. benzoxazinones
  75340. benzoxazocines
  75341. benzoxetes
  75342. benzoyl
  75343. benzoylethyl
  75344. benzoylformates
  75345. benzoylimidazoles
  75346. benzvalene
  75347. benzvalene
  75348. properties
  75349. synthetic
  75350. potential
  75351. benzyl
  75352. benzylamidine
  75353. benzylation
  75354. benzylfuran
  75355. benzylic
  75356. benzylidene
  75357. benzylideneacetone
  75358. benzylidenehexopyran
  75359. benzylimine
  75360. benzyllithium
  75361. benzylmalonates
  75362. benzyloxy
  75363. benzylpotassium
  75364. benzylrubidium
  75365. benzylselenides
  75366. benzyltrimethylammon
  75367. benzyne
  75368. benzyne-furan
  75369. benzynes
  75370. beoxytrichoviridin
  75371. berbine
  75372. bercaw
  75373. berdy
  75374. berdy
  75375. handbook
  75376. antibiotic
  75377. compounds
  75378. berendsen
  75379. berestovitskayaM
  75380. berezhnaya
  75381. berezovskii
  75382. bergan
  75383. bergbretter
  75384. bergdahl
  75385. berger
  75386. berger
  75387. brigitte
  75388. raadt
  75389. griengl
  75390. herfried
  75391. hayden
  75392. walter
  75393. berger
  75394. nuclear
  75395. magnetic
  75396. relaxation
  75397. recent
  75398. problems
  75399. bergeron
  75400. bergman
  75401. bergman
  75402. isotope
  75403. crossover
  75404. experiments
  75405. carbon
  75406. carbon
  75407. bergman-type
  75408. bergquist
  75409. bergstrom
  75410. bergstrom
  75411. xiaoping
  75412. guangyi
  75413. rotstein
  75414. david
  75415. bergter
  75416. berkeley
  75417. berkshire
  75418. berlinR
  75419. berlin
  75420. sherle
  75421. synthesis
  75422. properties
  75423. polyme
  75424. berliner
  75425. bernal
  75426. bernal
  75427. stereochemistry
  75428. organometallic
  75429. inorgan
  75430. bernard
  75431. bernardi
  75432. bernasconi
  75433. bernasconi
  75434. kinetic
  75435. behavior
  75436. short
  75437. lived
  75438. anionic
  75439. sigma
  75440. bernasconi
  75441. claude
  75442. principle
  75443. perfect
  75444. synchroniza
  75445. bernasconi
  75446. claude
  75447. principle
  75448. nonperfect
  75449. synchronizat
  75450. bernd
  75451. berneth
  75452. bernhard
  75453. bernhard
  75454. mayer
  75455. recent
  75456. advances
  75457. synthesis
  75458. berrisford
  75459. berry
  75460. berry
  75461. stephen
  75462. potential
  75463. surfaces
  75464. dynamics
  75465. cluster
  75466. bersohn
  75467. berson
  75468. berson
  75469. hypothetical
  75470. biradical
  75471. pathways
  75472. thermal
  75473. unimol
  75474. berson
  75475. chemistry
  75476. trimethylenemethanes
  75477. class
  75478. berson
  75479. jerome
  75480. overlap
  75481. component
  75482. stereoelectroni
  75483. berthiaume
  75484. berti
  75485. bertran
  75486. bertrand
  75487. bertrand
  75488. wentrup
  75489. nitrile
  75490. imines
  75491. matrix
  75492. charact
  75493. bertrand
  75494. recent
  75495. progress
  75496. sulfonyl
  75497. radicals
  75498. bertrand
  75499. michele
  75500. recent
  75501. progress
  75502. sulfonyl
  75503. bertucci
  75504. bertyadionol
  75505. beschke
  75506. beschke
  75507. reactions
  75508. cycloalkenopyridines
  75509. besses
  75510. besse
  75511. veschambre
  75512. chemical
  75513. biological
  75514. synthesis
  75515. bessiere
  75516. bestmann
  75517. bestmann
  75518. syntheses
  75519. reactions
  75520. polyelement
  75521. bestmann
  75522. zimmermann
  75523. alkylations
  75524. acylations
  75525. betar
  75526. lactams
  75527. retrospect
  75528. prospect
  75529. review
  75530. beta-addition
  75531. beta-adrenoceptor
  75532. beta-alkoxy
  75533. beta-amino
  75534. beta-d-galacto-oligo
  75535. beta-dicarbonyl
  75536. beta-epoxysilanes
  75537. beta-ethylenic
  75538. beta-functionalized
  75539. beta-hydroxy-alpha-a
  75540. beta-keto
  75541. beta-lactams
  75542. beta-oxygenated
  75543. beta-unsaturated
  75544. betain
  75545. betaine
  75546. betaines
  75547. betalains
  75548. bethell
  75549. bethell
  75550. carbocations
  75551. reactive
  75552. intermediates
  75553. jones
  75554. bethell
  75555. whittaker
  75556. carbocations
  75557. reactive
  75558. intermedia
  75559. bethune
  75560. betschinger
  75561. better
  75562. betwee
  75563. betweenC
  75564. beugelmans
  75565. beyerman
  75566. beyond
  75567. beyond
  75568. higher
  75569. fullerenes
  75570. bhaduri
  75571. bhaduri
  75572. amiya
  75573. synthetic
  75574. intermediates
  75575. biologically
  75576. bhandari
  75577. bhatia
  75578. bhatia
  75579. bhatnagar
  75580. bhatt
  75581. bhattacharya
  75582. bhattacharya
  75583. thyagarajan
  75584. michaelis
  75585. arbuzov
  75586. rearran
  75587. bhattacharyja
  75588. bhattacharyya
  75589. bhattacharyya
  75590. kankan
  75591. chowdhury
  75592. mihir
  75593. environmental
  75594. magne
  75595. bhupathy
  75596. bhupathy
  75597. hughes
  75598. amato
  75599. bergan
  75600. leazer
  75601. lovela
  75602. bhushan
  75603. bianchi
  75604. bianchi
  75605. micheli
  75606. gandolfi
  75607. dipolar
  75608. cycloreversions
  75609. bianka
  75610. biaryl
  75611. biaryls
  75612. biasi
  75613. bibliographies
  75614. bibliography
  75615. bicarbocyclic\
  75616. bichromophoric
  75617. sinchai
  75618. alkaloids
  75619. lauraceae
  75620. sinchai
  75621. phenanthroindolizidi
  75622. phenanthroquin
  75623. bickel
  75624. bickelhaupt
  75625. bickelhaupt
  75626. friedrich
  75627. carbenoid
  75628. routes
  75629. substituted
  75630. phosph
  75631. bickelhaupt
  75632. friedrich
  75633. willen
  75634. small
  75635. strained
  75636. bickelhaupt
  75637. friedrich
  75638. importance
  75639. intramolecular
  75640. solva
  75641. bicycl
  75642. bicycles
  75643. bicyclic
  75644. etals
  75645. synthesis
  75646. reactions
  75647. bicyclic
  75648. amidines
  75649. reagents
  75650. organic
  75651. synthesis
  75652. bicyclic
  75653. compounds
  75654. structurally
  75655. related
  75656. dehydroacetic
  75657. bicyclic
  75658. diazepines
  75659. diazepines
  75660. additional
  75661. bicyclic
  75662. ketals
  75663. versatile
  75664. intermediates
  75665. stereocontro
  75666. bicyclic
  75667. sesquiterpene
  75668. synthesis
  75669. intramolecular
  75670. cyclizat
  75671. bicyclic
  75672. triazoles
  75673. diazo
  75674. transfer
  75675. reaction
  75676. between
  75677. bicyclization
  75678. bicyclizations
  75679. bicyclo
  75680. bickelhaupt
  75681. friedrich
  75682. willen
  75683. small
  75684. strained
  75685. cycl@
  75686. bicyclic
  75687. amide
  75688. acetals
  75689. synthesis
  75690. reactions@
  75691. bicyclo
  75692. bicyclo
  75693. alkenes@
  75694. billups
  75695. synthesis
  75696. chemistry
  75697. benzocyclopropanes
  75698. binary@
  75699. binkley
  75700. photochemical
  75701. reactions
  75702. carbohydrates
  75703. bioactivities@
  75704. biochemistry
  75705. biological
  75706. biology@
  75707. biomimetic
  75708. biopolymers
  75709. biotechnology@
  75710. birkhofer
  75711. stuhl
  75712. silylated
  75713. synthons
  75714. facile
  75715. organic
  75716. reagen@
  75717. bis-cinchona@
  75718. bis-heteroannulation
  75719. total
  75720. synthesis
  75721. furanoterpenes
  75722. buten
  75723. blasius@
  75724. block
  75725. reactions
  75726. organosulphur
  75727. compounds
  75728. academic
  75729. press
  75730. jenkins
  75731. lawrence
  75732. recent
  75733. progress
  75734. synt@
  75735. boca@
  75736. bodanszky
  75737. martinez
  75738. reactions
  75739. peptide
  75740. synthesis
  75741. bognar
  75742. bowie
  75743. bimolecular
  75744. reactions
  75745. nucleophiles
  75746. bickelhaupt
  75747. friedrich
  75748. willen
  75749. small
  75750. strained
  75751. cycl@
  75752. cleavage
  75753. energies
  75754. molecules
  75755. their
  75756. associated
  75757. cimarusti
  75758. monobactams
  75759. expedi@
  75760. carless
  75761. howard
  75762. cyclohexa
  75763. diene
  75764. diols
  75765. chemical
  75766. chlorotrimethyl
  75767. silyl
  75768. accelerated
  75769. conjugate
  75770. addition
  75771. orga@
  75772. considerations
  75773. chiral
  75774. recognition
  75775. relevant
  75776. liquid
  75777. chro@
  75778. cyclizations@
  75779. davis
  75780. anthony
  75781. cholaphaneset
  75782. steroids
  75783. asstructural
  75784. compo@
  75785. diastereoselective
  75786. additions
  75787. using
  75788. cameo
  75789. cram's
  75790. asymmet@
  75791. donor-acceptor-subst
  75792. cyclopropanes
  75793. versatile
  75794. building
  75795. blocks@
  75796. elliott
  75797. progress
  75798. design
  75799. insecticides
  75800. ester
  75801. cleavages
  75802. sn2-type
  75803. dealkylation@
  75804. silylcarbinols
  75805. silaethylenes@
  75806. gilchrist
  75807. thomas
  75808. synthesis
  75809. membered
  75810. aromatic
  75811. heter@
  75812. guseva@
  75813. hegarty
  75814. stereospecific
  75815. reactions
  75816. nitrilium
  75817. bicyclo
  75818. alkenes
  75819. bicyclobutonium
  75820. bicyclohexanes
  75821. bidirectional
  75822. bidlingmeyer
  75823. bidlingmeyer
  75824. brian
  75825. practical
  75826. methodology
  75827. applicat
  75828. biehl
  75829. biellmann
  75830. biemann
  75831. biemann
  75832. klaus
  75833. analytical
  75834. techniques
  75835. trace
  75836. organic
  75837. compou
  75838. bienz
  75839. bierbaum
  75840. biermann
  75841. bifunctional
  75842. bifunctional
  75843. chiral
  75844. auxiliaries
  75845. aldol
  75846. reactions
  75847. enolate
  75848. biggadike
  75849. biginelli
  75850. bilha
  75851. bilirubinx
  75852. billington
  75853. billington
  75854. inositol
  75855. phosphates
  75856. chemical
  75857. synthesis
  75858. billion
  75859. billups
  75860. billups
  75861. mccord
  75862. phase
  75863. synthesis
  75864. reactive
  75865. molec
  75866. billups
  75867. synthesis
  75868. chemistry
  75869. benzocyclopropanes
  75870. billups
  75871. edward
  75872. ciufolini
  75873. marco
  75874. buckminsterfullerene
  75875. biloen
  75876. bimetallic
  75877. bimetallic
  75878. catalytic
  75879. systems
  75880. containing
  75881. titanium
  75882. zirconium
  75883. bimolecular
  75884. bimolecular
  75885. addition
  75886. epoxides
  75887. activated
  75888. olefins
  75889. bimolecular
  75890. formation
  75891. radicals
  75892. transfer
  75893. bimolecula
  75894. bimolecular
  75895. reactions
  75896. carbenes
  75897. membered
  75898. rings
  75899. binap
  75900. binap
  75901. efficient
  75902. chiral
  75903. element
  75904. asymmetric
  75905. catalysis
  75906. binaphthalenes
  75907. binaphthol
  75908. binaphthylic
  75909. binaphthyls
  75910. binaphyl
  75911. bindal
  75912. bindel
  75913. binders
  75914. binding
  75915. bindra
  75916. bindra
  75917. synthesis
  75918. prostaglandins
  75919. total
  75920. binkley
  75921. binkley
  75922. photochemical
  75923. reactions
  75924. carbohydrates
  75925. binne
  75926. binol
  75927. binsch
  75928. binsch
  75929. kessler
  75930. kinetic
  75931. mechanistic
  75932. evaluation
  75933. binst
  75934. binuclear
  75935. bioactive
  75936. bioactivity
  75937. bioamphiphiles
  75938. bioassay
  75939. biocatalysis
  75940. biocatalysts
  75941. biocatalytic
  75942. biochem
  75943. biochemical
  75944. biochemical
  75945. oxidations
  75946. biochemical
  75947. reductions
  75948. biochemiexcitation
  75949. biochemistry
  75950. biochemistry
  75951. bioconversion
  75952. biodegradation
  75953. bioformation
  75954. bioformation
  75955. optically
  75956. epoxides
  75957. biogenesis
  75958. biogenetic
  75959. biogenetically
  75960. biogenic
  75961. biohydroxlylation
  75962. biolgical
  75963. biolog
  75964. biologicai
  75965. biologicalU
  75966. biological
  75967. biological
  75968. applications
  75969. molecular
  75970. switches
  75971. biological
  75972. variation
  75973. microbial
  75974. metabolites
  75975. precursor-d
  75976. biological-systems
  75977. biologically
  75978. bioluminescence
  75979. biomarker
  75980. biomass
  75981. biomedical
  75982. biomembranes
  75983. biomimetic
  75984. biomimetic
  75985. biomimetic
  75986. alkane
  75987. oxidation
  75988. presence
  75989. complexe
  75990. biomimetic
  75991. catalysts
  75992. selective
  75993. oxidation
  75994. organic
  75995. biomimetic
  75996. chemistry
  75997. nickel
  75998. biomimetic
  75999. oxidation
  76000. organic
  76001. synthesis
  76002. using
  76003. transition
  76004. biomimetic
  76005. polyene
  76006. cyclisations
  76007. biomimetic
  76008. transformations
  76009. sesquiterpene
  76010. lactones
  76011. biomolecular
  76012. biomolecularhomochir
  76013. biomoleculeso
  76014. bioorganic
  76015. bioorganic
  76016. chemistry
  76017. chemical
  76018. approach
  76019. enzyme
  76020. action
  76021. bioorganic
  76022. chemistry
  76023. total
  76024. synthesis
  76025. tetra
  76026. polycyclic
  76027. bioorganometallic
  76028. bioorganometallic
  76029. chemistry
  76030. future
  76031. direction
  76032. transitio
  76033. bioorganosilicon
  76034. biophysical
  76035. biopolymers
  76036. biopolymers
  76037. biosynthesis
  76038. biosynthesis
  76039. esperamicin
  76040. enediyne
  76041. antitumor
  76042. antibio
  76043. biosynthesis
  76044. fatty
  76045. polyketide
  76046. metabolites
  76047. biosynthesis
  76048. pyrrolizidine
  76049. alkaloids
  76050. biosynthesis
  76051. heterocyclic
  76052. natural
  76053. products
  76054. biosynthesis
  76055. taxoids
  76056. attachment
  76057. taxol
  76058. biosynthetic
  76059. biosynthetic
  76060. biomimetic
  76061. related
  76062. epoxide
  76063. cyclizations
  76064. biosynthetic
  76065. biomimetic
  76066. related
  76067. epoxide
  76068. cyclizations
  76069. biotechnological
  76070. biotechnology
  76071. biotin
  76072. biotransform
  76073. biotransform
  76074. tions
  76075. organic
  76076. chemistry
  76077. biotransformation
  76078. biotransformation-a
  76079. biotransformations
  76080. biotransformations
  76081. preparative
  76082. organic
  76083. chemistry
  76084. biotransformations
  76085. peptide
  76086. carbohydrate
  76087. fields
  76088. biotransformations
  76089. relating
  76090. heterocyclic
  76091. compounds
  76092. biphenyl
  76093. biphenylene
  76094. biphenyleno
  76095. biphenyls
  76096. biphosphine
  76097. bipyridine
  76098. bipyridines
  76099. bipyrimidine
  76100. biquaryls
  76101. biradical
  76102. biradical
  76103. rearrangement
  76104. during
  76105. intramolecular
  76106. cycloaddition
  76107. biradicals
  76108. birch
  76109. electrochemistry
  76110. viologens
  76111. 198110
  76112. birds
  76113. birkett
  76114. birkhaeuserU
  76115. birkhofer
  76116. birkhofer
  76117. stuhl
  76118. silylated
  76119. synthons
  76120. facile
  76121. organic
  76122. reagen
  76123. birth
  76124. birthday
  76125. alkoxycarbonyl
  76126. telluriums
  76127. aminocarbonyl
  76128. hydrazi
  76129. othiocarbonyl
  76130. dibenzoyl
  76131. oligo
  76132. benzocrown
  76133. ether
  76134. cyclopentadienyl
  76135. zirconium
  76136. hafnium
  76137. compounds
  76138. diisopropylamino
  76139. phosphinyldiazometha
  76140. building
  76141. block
  76142. h-cyclopentadienyl
  76143. lanthanoid
  76144. chlorides
  76145. organoelement
  76146. peroxides
  76147. bis-adducts
  76148. bis-dienes
  76149. bis-heteroannulation
  76150. bis-heteroannulation
  76151. total
  76152. synthesis
  76153. furanoterpenes
  76154. buten
  76155. bis-heteroannulation
  76156. total
  76157. synthesis
  76158. furanoterpenes
  76159. buten
  76160. bis-homodiene
  76161. bis-lactim
  76162. bis-radical
  76163. bis-silyation
  76164. bis-silylation
  76165. bis-sulfides
  76166. bis-sulfones
  76167. bis-tetrahyrrofuran
  76168. bisacetals
  76169. bisalkylation
  76170. bisbenzylisoquinolin
  76171. bisboranes
  76172. bischler
  76173. bischler
  76174. napieralski
  76175. related
  76176. reactions
  76177. review
  76178. mecha
  76179. bischler-napieralski
  76180. biscyclizations
  76181. bishomocubane
  76182. bishomocubanes
  76183. bishomocubanone
  76184. bishop
  76185. bishydrazone
  76186. bisindole
  76187. bismabenzene
  76188. bismuthN
  76189. bismuthides
  76190. bismuthonium
  76191. bisnaphthalenes
  76192. bisphosphine
  76193. bisquinolizidine
  76194. bissell
  76195. bissell
  76196. richard
  76197. desilva
  76198. prasanna
  76199. gunaratne
  76200. nimal
  76201. bissig
  76202. bissolino
  76203. bistable
  76204. bithiazolyl
  76205. bitter
  76206. bjoern
  76207. bjorg
  76208. black
  76209. black
  76210. doyle
  76211. azabicyclo
  76212. 3.1.0
  76213. hexanes
  76214. analog
  76215. black
  76216. david
  76217. dimensions
  76218. indole
  76219. chemistry
  76220. blackborow
  76221. blackborow
  76222. young
  76223. metal
  76224. vapor
  76225. synthesis
  76226. organometali
  76227. blackburn
  76228. blackburn
  76229. wentworth
  76230. catalytic
  76231. antibodies
  76232. generatio
  76233. blackburn
  76234. michael
  76235. nucleic
  76236. acids
  76237. chemistry
  76238. biolog
  76239. blackett
  76240. blackie
  76241. blacklock
  76242. blackman
  76243. blackman
  76244. allan
  76245. reactions
  76246. coordinated
  76247. ligands
  76248. advances
  76249. blackwell
  76250. blagg
  76251. blagg
  76252. julian
  76253. stoichiometric
  76254. applications
  76255. organotransition
  76256. blaise
  76257. blake
  76258. blanc
  76259. blaney
  76260. blanka
  76261. blanz
  76262. blasberger
  76263. blaser
  76264. blaser
  76265. ulrich
  76266. enantioselective
  76267. synthesis
  76268. using
  76269. chiral
  76270. blaser
  76271. ulrich
  76272. chiral
  76273. source
  76274. enantiosel
  76275. blasius
  76276. blasius
  76277. janzen
  76278. analytical
  76279. applications
  76280. crown
  76281. compou
  76282. blasko
  76283. blaszczyk
  76284. blatt
  76285. halket
  76286. handbook
  76287. derivatives
  76288. chromatogr
  76289. blazevic
  76290. blazevic
  76291. kolbah
  76292. belin
  76293. sunjic
  76294. kajfei
  76295. hexamethylenet
  76296. blechert
  76297. bleeke
  76298. bleeke
  76299. metallabenzene
  76300. chemistry
  76301. accou
  76302. bleeke
  76303. metallabenzene
  76304. chemistry
  76305. accts
  76306. bleha
  76307. blenderman
  76308. blending
  76309. bleomycin
  76310. bleomycins
  76311. blewitt
  76312. blicke
  76313. blinka
  76314. blizzard
  76315. blizzard
  76316. recent
  76317. progress
  76318. synthesis
  76319. avermectins
  76320. bllis
  76321. block
  76322. block
  76323. deorazio
  76324. chemistry
  76325. salad
  76326. comparative
  76327. block
  76328. organic
  76329. sulfur
  76330. compounds
  76331. organic
  76332. synthesis
  76333. 197811
  76334. block
  76335. reactions
  76336. organosulphur
  76337. compounds
  76338. academic
  76339. press
  76340. block
  76341. cyclophanes
  76342. monographs
  76343. supramolecular
  76344. chemi
  76345. blocking
  76346. blocking
  76347. protection
  76348. alpha-carboxy
  76349. function
  76350. blocking
  76351. protection
  76352. alpha-amino
  76353. function
  76354. pepti
  76355. blocks
  76356. blokzijl
  76357. blokzijl
  76358. wilfried
  76359. engberts
  76360. hydrophobic
  76361. effects
  76362. blomberg
  76363. blomberg
  76364. cornelis
  76365. barbier
  76366. reaction
  76367. related
  76368. blondet
  76369. blood
  76370. bloodworth
  76371. bloom
  76372. bloomfield
  76373. bloxsidge
  76374. blue-transperent
  76375. blumbach
  76376. blumberg
  76377. blumenkopf
  76378. blunden
  76379. blystone
  76380. blyumberg
  76381. jenkins
  76382. lawrence
  76383. recent
  76384. progress
  76385. boavida
  76386. bobbitt
  76387. bobbitt
  76388. kulkarni
  76389. willis
  76390. electrooxidation
  76391. bobkova
  76392. bobrovskii
  76393. amino
  76394. protecting
  76395. group
  76396. boc-pyrrolidine
  76397. boche
  76398. boche
  76399. gernot
  76400. penetrated
  76401. pairs
  76402. bochkov
  76403. bochkov
  76404. zaikov
  76405. afanasiev
  76406. carbohydrates
  76407. utrec
  76408. bochkov
  76409. zaikov
  76410. chemistry
  76411. glycosidic
  76412. ruppert
  76413. klaus
  76414. nather
  76415. christian
  76416. havlas
  76417. zdenek
  76418. herrm
  76419. bockman
  76420. boczon
  76421. boczon
  76422. wladyslaw
  76423. stereochemical
  76424. aspects
  76425. bisquinolizidine
  76426. bodanszky
  76427. bodanszky
  76428. active
  76429. esters
  76430. peptide
  76431. synthesis
  76432. peptides
  76433. bodanszky
  76434. martinez
  76435. reactions
  76436. peptide
  76437. synthesis
  76438. bodanszky
  76439. miklos
  76440. peptide
  76441. chemistry
  76442. practical
  76443. textbook
  76444. bodanszky
  76445. miklos
  76446. principles
  76447. peptide
  76448. synthesis
  76449. bodor
  76450. bodrikov
  76451. bodurow
  76452. boeckel
  76453. boeckman
  76454. boehmer
  76455. boehmer
  76456. volker
  76457. walter
  76458. calix
  76459. arenes
  76460. bridged
  76461. boekelheide
  76462. boekelheide
  76463. cyclophanes
  76464. paracyclophane
  76465. superphane
  76466. boelens
  76467. boelins
  76468. boelins
  76469. linde
  76470. rijke
  76471. valois
  76472. boens
  76473. boerje
  76474. bogan
  76475. bogatkov
  76476. bogatskii
  76477. bogdan
  76478. bogdanovic
  76479. bogdanovic
  76480. selectivity
  76481. control
  76482. nickel
  76483. catalyzed
  76484. olefin
  76485. boger
  76486. boger
  76487. design
  76488. synthesis
  76489. evaluation
  76490. minor
  76491. groov
  76492. boger
  76493. design
  76494. synthesis
  76495. evaluation
  76496. functional
  76497. boger
  76498. duocarmycins
  76499. class
  76500. sequence
  76501. selective
  76502. bognar
  76503. bognar
  76504. bogulavskaya
  76505. bogumil
  76506. boguslavskaya
  76507. bohlmann
  76508. bohlmann
  76509. folding
  76510. squalene
  76511. problem
  76512. bohme
  76513. bohme
  76514. viehe
  76515. iminium
  76516. salts
  76517. organic
  76518. chemistry
  76519. bohmer
  76520. bohumil
  76521. boiadjievx
  76522. boiadjiev
  76523. lightner
  76524. synthetic
  76525. strategies
  76526. under
  76527. choussy
  76528. barbier
  76529. isomerizations
  76530. cyclizations
  76531. boivin
  76532. boivinase
  76533. boivinose
  76534. bokanov
  76535. bokanov
  76536. stpanov
  76537. chemistry
  76538. dihydrophenophosphaz
  76539. boland
  76540. boland
  76541. wilhelm
  76542. froessl
  76543. christian
  76544. lorenz
  76545. michael
  76546. esterolytic
  76547. boleslawski
  76548. bolker
  76549. carsten
  76550. enantioselective
  76551. transition
  76552. metal
  76553. catalyzed
  76554. bologna
  76555. bolotin
  76556. bolscher
  76557. boltond
  76558. bolton
  76559. cyclohexane
  76560. derivatives
  76561. second
  76562. supplements
  76563. bonacic
  76564. bonar
  76565. bonar
  76566. mackay
  76567. walter
  76568. marvaud
  76569. sanders
  76570. molecules
  76571. their
  76572. associated
  76573. dissociation
  76574. energy
  76575. values
  76576. silicon-containing
  76577. compou
  76578. energies
  76579. solution
  76580. electrode
  76581. potentials
  76582. hybridization
  76583. transition
  76584. metal
  76585. complexes
  76586. stereoele
  76587. bond-forming
  76588. bonded
  76589. bonding
  76590. bonding
  76591. group
  76592. elements
  76593. bondo
  76594. bondsF
  76595. bonds
  76596. bone-active
  76597. bonini
  76598. bonini
  76599. carlo
  76600. righi
  76601. giuliana
  76602. regio
  76603. chemoselective
  76604. synthes
  76605. bonium
  76606. bonjoch
  76607. bonnemann
  76608. bonnemann
  76609. cobalt
  76610. catalyzed
  76611. pyridine
  76612. syntheses
  76613. alkynes
  76614. bonner
  76615. bonnet
  76616. bonnett
  76617. bonnett
  76618. north
  76619. chemistry
  76620. isoindoles
  76621. books
  76622. boone
  76623. boone
  76624. ashby
  76625. reduction
  76626. cyclic
  76627. bicyclic
  76628. ketones
  76629. borabicyclo
  76630. boracarbenoid
  76631. boraheterocycles
  76632. borane
  76633. borane
  76634. reagents
  76635. borane-dimethyl
  76636. boranes
  76637. borates
  76638. borazaromatic
  76639. borden
  76640. borden
  76641. davidson
  76642. theoretical
  76643. studies
  76644. diradicals
  76645. borden
  76646. diradicals
  76647. reactive
  76648. intermediates
  76649. jones
  76650. borden
  76651. diradicals
  76652. reactive
  76653. intermediates
  76654. jones
  76655. borden
  76656. weston
  76657. thatcher
  76658. iwamura
  76659. hiizu
  76660. berson
  76661. jerome
  76662. violati
  76663. border
  76664. borderlines
  76665. borders
  76666. bordetella
  76667. bordwell
  76668. boren
  76669. borepins
  76670. borepins
  76671. group
  76672. element
  76673. heteroles
  76674. borghi
  76675. boride
  76676. borinate
  76677. borinates
  76678. borirenes
  76679. boris
  76680. borisov
  76681. borisova
  76682. boriz
  76683. borman
  76684. borneol
  76685. bornyl
  76686. borobicyclo
  76687. borohydride
  76688. borohydrides
  76689. borono
  76690. boron-carbon
  76691. boron-carbon
  76692. ligands
  76693. organometallic
  76694. synthesis
  76695. boron-catalyzed
  76696. boron-nitrogen
  76697. boron-phosphorus
  76698. boron-phosphorus
  76699. compounds
  76700. multiple
  76701. bonding
  76702. boron-substituted
  76703. boron-substituted
  76704. heteroaromatic
  76705. compounds
  76706. boron-zinc
  76707. ronates
  76708. boronic
  76709. boronic
  76710. esters
  76711. stereodirected
  76712. synthesis
  76713. borothel
  76714. borovkov
  76715. borthwick
  76716. borthwick
  76717. biggadike
  76718. keith
  76719. synthesis
  76720. chiral
  76721. carbocy
  76722. bortiatynski
  76723. bortolini
  76724. bortylsubstituent
  76725. borylation
  76726. bosch
  76727. bosch
  76728. bonjoch
  76729. synthesis
  76730. azabicyclo
  76731. 3.3.1
  76732. nonanes
  76733. manhas
  76734. tavares
  76735. fujiwara
  76736. bosnich
  76737. bosnich
  76738. fryzuk
  76739. asymmetric
  76740. synthesis
  76741. mediated
  76742. transi
  76743. bosons
  76744. bossert
  76745. bossert
  76746. meyers
  76747. wehinger
  76748. aryldihydropyridines
  76749. bostonU
  76750. boswell
  76751. botryococcus
  76752. alkenediazonium
  76753. salts
  76754. chapter
  76755. classical
  76756. coupling
  76757. solvolysis
  76758. linkage
  76759. promising
  76760. bottcher
  76761. botteghi
  76762. botteghi
  76763. carlo
  76764. paganelli
  76765. stefano
  76766. schionato
  76767. alberto
  76768. marchetti
  76769. bottom
  76770. bouas
  76771. bouchere
  76772. bouillon
  76773. bouillon
  76774. maliverney
  76775. janousek
  76776. viehe
  76777. boullanger
  76778. boulton
  76779. bound
  76780. boureier
  76781. bourque
  76782. bouvardin
  76783. bouzard
  76784. bowden
  76785. bowden
  76786. compounds
  76787. carbon
  76788. sigma
  76789. bonds
  76790. bowden
  76791. kenneth
  76792. grubbs
  76793. edward
  76794. angular
  76795. dependence
  76796. dipolar
  76797. bowen
  76798. bowen
  76799. williams
  76800. phase
  76801. rearrangements
  76802. rearrang
  76803. bowen
  76804. williams
  76805. schwarz
  76806. chemistry
  76807. isolated
  76808. bowen
  76809. richard
  76810. neutral
  76811. complexes
  76812. accts
  76813. research
  76814. bowie
  76815. bowie
  76816. bimolecular
  76817. reactions
  76818. nucleophiles
  76819. bowman
  76820. bowser
  76821. bowser
  76822. organometallic
  76823. derivatives
  76824. fullerenes
  76825. advances
  76826. vernon
  76827. relationship
  76828. between
  76829. order
  76830. vernon
  76831. interactions
  76832. vernon
  76833. significance
  76834. lengths
  76835. boxyl
  76836. olivier
  76837. brossi
  76838. arnold
  76839. tropolonic
  76840. colchicum
  76841. alkaloids
  76842. boyer
  76843. boyer
  76844. increasing
  76845. index
  76846. covalent
  76847. oxygen
  76848. bonding
  76849. boykin
  76850. boykin
  76851. david
  76852. spectroscopy
  76853. organic
  76854. chemistry
  76855. boyland-sims
  76856. brabham
  76857. braca
  76858. bracher
  76859. brachwitz
  76860. brackelaire
  76861. bradley
  76862. bradley
  76863. mehrotra
  76864. metal
  76865. alkoxides
  76866. academic
  76867. bradshaw
  76868. bradshaw
  76869. izatt
  76870. christensen
  76871. synthetic
  76872. bradshaw
  76873. stott
  76874. preparation
  76875. derivatives
  76876. analog
  76877. bradshaw
  76878. synthesis
  76879. multidentate
  76880. compounds
  76881. synthetic
  76882. bradshaw
  76883. jerald
  76884. krakowiak
  76885. krzysztof
  76886. izatt
  76887. bradshaw
  76888. jerald
  76889. krakowiak
  76890. krzysztof
  76891. izatt
  76892. prepara
  76893. bradsher
  76894. brady
  76895. brady
  76896. synthetic
  76897. applications
  76898. involving
  76899. halogenated
  76900. keten
  76901. braekman
  76902. braeutler
  76903. braga
  76904. braga
  76905. dario
  76906. dynamical
  76907. processes
  76908. crystalline
  76909. organometalli
  76910. bragg
  76911. bragg
  76912. dennis
  76913. ferguson
  76914. howell
  76915. morga
  76916. bragin
  76917. braish
  76918. braithwaite
  76919. braithwaite
  76920. nalcolm
  76921. ketteman
  76922. clare
  76923. taking
  76924. trash
  76925. branca
  76926. branched
  76927. branches
  76928. branching
  76929. brand
  76930. brand
  76931. young
  76932. silverstein
  76933. insect
  76934. pheromones
  76935. branda
  76936. brandi
  76937. bradshaw
  76938. izatt
  76939. christensen
  76940. synthetic
  76941. brandi
  76942. alberto
  76943. cicchi
  76944. stefano
  76945. andrea
  76946. pietrusiewicz
  76947. breakthrough
  76948. bregadze@
  76949. brewster
  76950. marcus
  76951. huang
  76952. bodor
  76953. nicholas
  76954. cont@
  76955. bridgehead
  76956. radicals
  76957. britton
  76958. bromination@
  76959. bromoarylalkanoic
  76960. brophy
  76961. cavill
  76962. naturally
  76963. occurring
  76964. pyrazines
  76965. brown
  76966. campbell
  76967. synthesis
  76968. applications
  76969. viny@
  76970. bruice
  76971. buchwald@
  76972. walsh
  76973. intracellular
  76974. steps
  76975. bacterial
  76976. alpha
  76977. alpha
  76978. oligopyridines
  76979. buncel
  76980. wilson
  76981. initial
  76982. state
  76983. transition
  76984. state
  76985. solvent
  76986. burgess
  76987. vicky
  76988. davies
  76989. stephen
  76990. skerlj
  76991. renato
  76992. mimics@
  76993. butadianylmalonates@
  76994. butyldimethylsiloxy@
  76995. soccolini
  76996. synthesis
  76997. malonaldehyde
  76998. cimarusti
  76999. monobactams
  77000. expedi
  77001. brandi
  77002. alberto
  77003. cicchi
  77004. stefano
  77005. andrea
  77006. pietrusiewicz
  77007. brandi
  77008. alberto
  77009. cordero
  77010. franca
  77011. sarlo
  77012. francesco
  77013. brandon
  77014. brandsma
  77015. brandsma
  77016. preparative
  77017. polar
  77018. organometallic
  77019. chemistry
  77020. brandstrom
  77021. brandt
  77022. brandukova
  77023. brandukova
  77024. vygodskii
  77025. vinogradova
  77026. branko
  77027. braslavsky
  77028. brassinolide
  77029. brassinosteroid
  77030. brassinosteroids
  77031. braterman
  77032. braterman
  77033. orbital
  77034. correlation
  77035. making
  77036. breaking
  77037. brauer
  77038. brauman
  77039. braun
  77040. braun
  77041. andre
  77042. jakob
  77043. laurent
  77044. oliveros
  77045. esther
  77046. oller
  77047. nascime
  77048. braun
  77049. manfred
  77050. recent
  77051. developments
  77052. stereoselective
  77053. aldol
  77054. braunii
  77055. braunstein
  77056. braverman
  77057. bravo
  77058. bravo
  77059. pierfrancesco
  77060. resnati
  77061. guiseppe
  77062. preparation
  77063. propert
  77064. brcf2cf2i
  77065. breach
  77066. break
  77067. breaking
  77068. breakthrough
  77069. breakthrough
  77070. breast
  77071. breathing
  77072. bredas
  77073. bredas
  77074. adant
  77075. tackx
  77076. persoons
  77077. pierce
  77078. third
  77079. order
  77080. bredt
  77081. bredt
  77082. compounds
  77083. bredt
  77084. bredt's
  77085. bredt's
  77086. brefeldin
  77087. bregadze
  77088. dicarba
  77089. closo
  77090. dodecaboranes
  77091. c2biohi2
  77092. their
  77093. bregadze
  77094. kampel
  77095. usyatinskii
  77096. godovikov
  77097. breitgoff
  77098. breitmaier
  77099. breitmaier
  77100. structure
  77101. elucidation
  77102. organic
  77103. chemist
  77104. bremner
  77105. dubonosov
  77106. minkin
  77107. chernoivanov
  77108. norbornad
  77109. brennan
  77110. brent
  77111. bresciani
  77112. breslow
  77113. breslow
  77114. biomimetic
  77115. control
  77116. chemical
  77117. selectivity
  77118. breslow
  77119. ronald
  77120. hydrophobic
  77121. effects
  77122. simple
  77123. organic
  77124. reactio
  77125. breuer
  77126. brevetoxin
  77127. brevetoxin
  77128. chemical
  77129. modifications
  77130. synaptosome
  77131. binding
  77132. brewster
  77133. brewster
  77134. marcus
  77135. huang
  77136. bodor
  77137. nicholas
  77138. breysse
  77139. brezgunov
  77140. brezhnev
  77141. brian
  77142. brice
  77143. bridge
  77144. bridged]
  77145. bridged
  77146. valence
  77147. isomers
  77148. benzene
  77149. cyclophanes
  77150. bridgehead
  77151. bridgehead
  77152. carbocations
  77153. solvolytic
  77154. study
  77155. bromobicyclo
  77156. bridgehead
  77157. carbocations
  77158. formation
  77159. bicyclo
  77160. 2.1.1
  77161. hexyl
  77162. bridgehead
  77163. intermediates
  77164. organic
  77165. synthesis
  77166. construction
  77167. bridgehead
  77168. olefins
  77169. small-ring
  77170. propellanes
  77171. bridgehead
  77172. radicals
  77173. bridgehead
  77174. radicals
  77175. bridges
  77176. bridging
  77177. brief
  77178. brieger
  77179. brieger
  77180. bennett
  77181. intramolecular
  77182. diels
  77183. alder
  77184. reactio
  77185. brienne
  77186. briggs
  77187. brigitte
  77188. brijoux
  77189. brill
  77190. brill
  77191. thomas
  77192. james
  77193. kenneth
  77194. kinetics
  77195. mechanisms
  77196. brillon
  77197. brillon
  77198. denis
  77199. recent
  77200. developments
  77201. thionation
  77202. brindaban
  77203. bringmann
  77204. brinhnan
  77205. brinker
  77206. brinkmeyer
  77207. bristol
  77208. bristow
  77209. britain
  77210. brittain
  77211. britton
  77212. britton
  77213. britton
  77214. carotenoids
  77215. polyterpenoids
  77216. britton
  77217. carotenoids
  77218. polyterpenoids
  77219. natural
  77220. broadbent
  77221. broadhurst
  77222. brobel
  77223. brodesser
  77224. brodesser
  77225. cuether
  77226. meier
  77227. ottens
  77228. hildebrandt
  77229. brodskaya
  77230. brodskaya
  77231. ratovskii
  77232. voronkov
  77233. orbital
  77234. interaction
  77235. broek
  77236. broeker
  77237. broken
  77238. bromide
  77239. bromides
  77240. nation
  77241. brominations
  77242. bromine
  77243. bromine
  77244. compounds
  77245. chemistry
  77246. applications
  77247. bromine-containi
  77248. bromo
  77249. bromoacetates
  77250. bromoacetonitrile
  77251. bromoalkyl
  77252. bromoalkynes
  77253. bromoamides
  77254. bromoamides
  77255. starting
  77256. materials
  77257. synthesis
  77258. bromoarenes
  77259. bromoaromatic
  77260. bromoaryl
  77261. bromoarylalkanoic
  77262. bromoarylalkanoic
  77263. bromobicyclo
  77264. bromobiphenyl
  77265. bromocarbocations
  77266. bromoesters
  77267. bromoetherification
  77268. bromoethyl
  77269. bromoform
  77270. bromohydrins
  77271. bromoisobutyrate
  77272. bromomagnesium
  77273. bromomethyl
  77274. bromomethyldimethyls
  77275. bromomethylene
  77276. bromonium
  77277. bromonium
  77278. p-bromocarbocations
  77279. olefin
  77280. bromination
  77281. bromotrimethylsilane
  77282. bromoxone
  77283. bronsted
  77284. bronsted
  77285. assisted
  77286. chiral
  77287. lewis
  77288. catalyst
  77289. brook
  77290. brook
  77291. bassindale
  77292. molecular
  77293. rearrangements
  77294. organos
  77295. brook
  77296. michael
  77297. henry
  77298. courtney
  77299. jueschkke
  77300. pankaj
  77301. brookhart
  77302. brooks
  77303. brooks
  77304. watson
  77305. terpenoid
  77306. phytoalexins
  77307. brooks
  77308. watson
  77309. terpenoid
  77310. phytoalexins
  77311. natural
  77312. brooks
  77313. charles
  77314. david
  77315. simulations
  77316. peptide
  77317. confo
  77318. broom
  77319. brophy
  77320. brophy
  77321. cavill
  77322. naturally
  77323. occurring
  77324. pyrazines
  77325. brossi
  77326. brotherton
  77327. brown
  77328. brown
  77329. chirality
  77330. design
  77331. synthesis
  77332. academic
  77333. brown
  77334. dearg
  77335. paquette
  77336. survey
  77337. epoxycyclodeca
  77338. brown
  77339. ragault
  77340. syntheses
  77341. homosteroids
  77342. brown
  77343. wolken
  77344. liquid
  77345. crystals
  77346. biological
  77347. structur
  77348. brown
  77349. campbell
  77350. synthesis
  77351. applications
  77352. brown
  77353. jadhav
  77354. mandal
  77355. asymmetric
  77356. synthesis
  77357. brown
  77358. krishnamurthy
  77359. boranes
  77360. organic
  77361. reductions
  77362. brown
  77363. krishnamurthy
  77364. forty
  77365. years
  77366. hydride
  77367. reductions
  77368. brown
  77369. meerwein
  77370. equilibrating
  77371. carbocations
  77372. brown
  77373. herbert
  77374. ramachandran
  77375. recent
  77376. advances
  77377. brown
  77378. herbert
  77379. ramachandran
  77380. veeraraghavan
  77381. asymmetric
  77382. brown
  77383. selectivity
  77384. mechanism
  77385. catalytical
  77386. asymme
  77387. brown
  77388. pyrolytic
  77389. methods
  77390. organic
  77391. chemistry
  77392. applicati
  77393. brown
  77394. roger
  77395. eastwood
  77396. frank
  77397. phase
  77398. chemistry
  77399. brownbridge
  77400. browne
  77401. brownlee
  77402. broxterman
  77403. bruce
  77404. bruce
  77405. michael
  77406. white
  77407. allan
  77408. chemistry
  77409. pentakis
  77410. bruckner
  77411. brudsail
  77412. bruening
  77413. brugger
  77414. bruice
  77415. bruice
  77416. bruneau
  77417. bruneau
  77418. christian
  77419. neveux
  77420. muriel
  77421. kabouche
  77422. zahia
  77423. ruppin
  77424. christ
  77425. brunet
  77426. brunner
  77427. brunner
  77428. chiral
  77429. metal
  77430. atoms
  77431. optically
  77432. active
  77433. organo
  77434. brunner
  77435. natural
  77436. products
  77437. enantioselective
  77438. catalysis
  77439. brunner
  77440. optical
  77441. induction
  77442. organo
  77443. transition
  77444. metal
  77445. compo
  77446. brunner
  77447. henri
  77448. enantioselective
  77449. rhodium
  77450. catalysts
  77451. brunner
  77452. henri
  77453. optical
  77454. activity
  77455. organic
  77456. chemistry
  77457. brunner
  77458. henri
  77459. zettlmeier
  77460. wolfgang
  77461. handbook
  77462. enantioselecti
  77463. bruno
  77464. brunsvigine
  77465. brunvollR
  77466. bruson
  77467. bryan
  77468. bryant
  77469. bryante
  77470. bryce
  77471. bryce
  77472. vernon
  77473. reactions
  77474. benzyne
  77475. heterocyclic
  77476. bryce
  77477. smith
  77478. gilbert
  77479. rearrangements
  77480. benzene
  77481. brycki
  77482. bryon
  77483. bryophites
  77484. bryophyta
  77485. bryostatin
  77486. bryostatins
  77487. bryson
  77488. bstituted
  77489. bu3snchbr2
  77490. bu3snh
  77491. bu3snh-bu4nx
  77492. bu3snsime3
  77493. bu4nbh4
  77494. bublitz
  77495. bubnov
  77496. buchachenko
  77497. buchanan
  77498. buchecker
  77499. buchel
  77500. bucher
  77501. bucherer
  77502. buchi
  77503. buchnerine
  77504. mechanistic
  77505. aspects
  77506. organophosphorus
  77507. chemistry
  77508. bucke
  77509. buckingham
  77510. buckingham
  77511. legon
  77512. roberts
  77513. principles
  77514. molec
  77515. buckminsterfullerene
  77516. buckminsterfullerene
  77517. great
  77518. balls
  77519. carbon
  77520. buckminsterfullerene
  77521. third
  77522. allotrope
  77523. carbon
  77524. buckus
  77525. buckwalter
  77526. andrzej
  77527. heyde
  77528. thomas
  77529. mislow
  77530. quantifyi
  77531. budapest
  77532. budyka
  77533. budyka
  77534. kantor
  77535. alfimov
  77536. photochemistry
  77537. phenyl
  77538. budzikiewicz
  77539. budzikiewicz
  77540. spectrometry
  77541. negative
  77542. analyt
  77543. bugaenko
  77544. walsh
  77545. intracellular
  77546. steps
  77547. bacterial
  77548. builders
  77549. building
  77550. building
  77551. blocks
  77552. dendritic
  77553. macromolecules
  77554. building
  77555. blocks
  77556. total
  77557. synthesis
  77558. anthracyclinones
  77559. building-blocks
  77560. builds
  77561. bukhtiarov
  77562. bukhtiarov
  77563. tomilov
  77564. cathodic
  77565. coupling
  77566. reactions
  77567. bulgarian
  77568. bulgecinine
  77569. bulky
  77570. bulky
  77571. supracyclopentadieny
  77572. derivatives
  77573. organometallic
  77574. alpha
  77575. alpha
  77576. oligopyridines
  77577. design
  77578. synthesis
  77579. properties
  77580. diels
  77581. alder
  77582. reaction
  77583. azadien
  77584. enantioselective
  77585. catalysis
  77586. fluorinated
  77587. heterocycles
  77588. target
  77589. model
  77590. studies
  77591. directed
  77592. towards
  77593. synthesis
  77594. reactions
  77595. synthesis
  77596. indole
  77597. alkaloids
  77598. bulletin
  77599. bulliot
  77600. bulmam
  77601. bulman
  77602. bumgardner
  77603. buncel
  77604. buncel
  77605. menon
  77606. spectrophotometric
  77607. investigations
  77608. arylme
  77609. buncel
  77610. saunders
  77611. isotopes
  77612. organic
  77613. chemistry
  77614. buncel
  77615. wilson
  77616. initial
  77617. state
  77618. transition
  77619. state
  77620. solvent
  77621. buncel
  77622. wilson
  77623. initial
  77624. state
  77625. transition
  77626. state
  77627. solvent
  77628. bundel
  77629. bundle
  77630. bunds
  77631. bunel
  77632. bunnelle
  77633. bunnelle
  77634. william
  77635. preparation
  77636. properties
  77637. reactions
  77638. bunnett
  77639. bunnett
  77640. aromatic
  77641. substitution
  77642. mechanism
  77643. bunnett
  77644. joseph
  77645. radical
  77646. chain
  77647. electron
  77648. transfer
  77649. dehalogenat
  77650. bunone
  77651. bunting
  77652. bunting
  77653. heterocyclic
  77654. pseudobases
  77655. advances
  77656. bunton
  77657. polyynes
  77658. fascinating
  77659. monomers
  77660. constructio
  77661. bureau
  77662. bures
  77663. bures
  77664. martin
  77665. yvonne
  77666. willett
  77667. peter
  77668. searching
  77669. techniq
  77670. burfitt
  77671. burger
  77672. burger
  77673. pentacoordinate
  77674. phosphoranes
  77675. synthesis
  77676. organopho
  77677. burgess|
  77678. burgess
  77679. sherman
  77680. asymmetric
  77681. syntheses
  77682. burgess
  77683. kevin
  77684. henderson
  77685. synthetic
  77686. approaches
  77687. stereois
  77688. burgess
  77689. kevin
  77690. ohlmeyer
  77691. michael
  77692. transition
  77693. metal
  77694. promoted
  77695. burgess
  77696. vicky
  77697. davies
  77698. stephen
  77699. skerlj
  77700. renato
  77701. mimics
  77702. burgoyne
  77703. burke
  77704. burke
  77705. grieco
  77706. intramolecular
  77707. reactions
  77708. diazocarbon
  77709. burkert
  77710. burkhardt
  77711. burmakov
  77712. burnaeva
  77713. burnell
  77714. burns
  77715. burns
  77716. christopher
  77717. saturated
  77718. oxygen
  77719. heterocycles
  77720. contempora
  77721. burrell
  77722. burrington
  77723. burrows
  77724. burrows
  77725. rokita
  77726. recognition
  77727. guanine
  77728. structure
  77729. bursian
  77730. bursten
  77731. bursten
  77732. bruce
  77733. comments
  77734. approximate
  77735. molecular
  77736. bursten
  77737. bruce
  77738. strittmatter
  77739. richard
  77740. cyclopentadienyl
  77741. burton
  77742. burton
  77743. donald
  77744. fluorinated
  77745. organometallics
  77746. burton
  77747. donald
  77748. morken
  77749. peter
  77750. fluorinated
  77751. burwell
  77752. busby
  77753. buscemi
  77754. buschmann
  77755. buschmann
  77756. helmut
  77757. scharf
  77758. dieter
  77759. hoffmann
  77760. norbert
  77761. esser
  77762. bushkov
  77763. business
  77764. butadianylmalonates
  77765. butadiene
  77766. butadiene-iron
  77767. butadienes
  77768. butadienoates
  77769. butadienyl
  77770. butadiynyl
  77771. butane
  77772. butanediols
  77773. butatrienes
  77774. butcher
  77775. buteneF
  77776. buteneolide
  77777. buteneolide
  77778. synthesis
  77779. based
  77780. contra-electronic
  77781. additio
  77782. butenoate
  77783. butenolide
  77784. butenolide
  77785. synthesis
  77786. based
  77787. contra
  77788. electronic
  77789. addition
  77790. butenolides
  77791. butenschon
  77792. butenschon
  77793. holger
  77794. construction
  77795. carbon
  77796. frame
  77797. works
  77798. butin
  77799. butler
  77800. butler
  77801. anthony
  77802. artemisinin
  77803. qinghaosu
  77804. butler
  77805. richard
  77806. oshea
  77807. donal
  77808. substituted123
  77809. triazolium
  77810. butoxide
  77811. butoxycarbonyl
  77812. butterworth
  77813. butyl
  77814. butyldimethylsiloxy
  77815. butyldimethylsilyldi
  77816. butyllithium
  77817. butyloxycarbonyl
  77818. butylphenyl
  77819. butylpyridine
  77820. butylspiro
  77821. butylstannyl
  77822. butylsulfonyl
  77823. butyltetrahedrane
  77824. butyltin
  77825. butyn
  77826. butyrolactone
  77827. butyrolactones
  77828. buxaceae
  77829. buyck
  77830. buyers
  77831. buyers
  77832. peter
  77833. canty
  77834. allan
  77835. honeyman
  77836. thomas
  77837. organometallic
  77838. symmetric
  77839. aziridines
  77840. class
  77841. chiral
  77842. ligand
  77843. bunton
  77844. micellar
  77845. catalysis
  77846. inhibition
  77847. henrick
  77848. synthesis
  77849. insect
  77850. pheromones
  77851. ramsden
  77852. mesomeric
  77853. betaine
  77854. derivatives
  77855. heteropentalene
  77856. tolman
  77857. steric
  77858. effects
  77859. phosphorus
  77860. ligands
  77861. organomet
  77862. blomberg
  77863. hartog
  77864. barbier
  77865. reaction
  77866. alternat
  77867. botteghi
  77868. soccolini
  77869. synthesis
  77870. malonaldehyde
  77871. gutsche
  77872. tetrahedron
  77873. synthes
  77874. djerassi
  77875. natural
  77876. products
  77877. peishoff
  77878. jorgensen
  77879. compu
  77880. kabalka
  77881. tetrahedron
  77882. catecholbor
  77883. reduction
  77884. organic
  77885. compounds
  77886. selective
  77887. reductions
  77888. borane
  77889. complexes
  77890. synthesis
  77891. sodium
  77892. cyanoborohydride
  77893. highly
  77894. stirling
  77895. sulfonium
  77896. salts
  77897. organic
  77898. chemistry
  77899. sulfur
  77900. stirling
  77901. tetrahedron
  77902. evaluation
  77903. suckling
  77904. suckling
  77905. enzymes
  77906. bradsher
  77907. formation
  77908. membered
  77909. cutler
  77910. heterocycl
  77911. chemist
  77912. kashima
  77913. yamamoto
  77914. tsuda
  77915. reaction
  77916. dimethyl
  77917. cimarusti
  77918. monobactams
  77919. expedi
  77920. morin
  77921. beugelmans
  77922. action
  77923. hydroxylamine
  77924. hydrazine
  77925. chemistry
  77926. biochemistry
  77927. amino
  77928. acids
  77929. narayana
  77930. periasamy
  77931. synthesis
  77932. organic
  77933. synthe
  77934. okafor
  77935. chemistry
  77936. applications
  77937. analog
  77938. gustorf
  77939. primary
  77940. photoprocesses
  77941. johnson
  77942. aldrichimica
  77943. applications
  77944. reichardt
  77945. halbritter
  77946. angew
  77947. rondesvedt
  77948. arylation
  77949. unsaturated
  77950. compounds
  77951. diazoni
  77952. structural
  77953. studies
  77954. thebtaranonth
  77955. thebtaranonth
  77956. pittman
  77957. vinyl
  77958. polymerization
  77959. organic
  77960. monomers
  77961. sonntag
  77962. sehuchmann
  77963. photolysis
  77964. saturated
  77965. spangler
  77966. thermal
  77967. sigmatropic
  77968. wentrup
  77969. fortschritte
  77970. forschung
  77971. rearra
  77972. cimarusti
  77973. monobactams
  77974. expedi@
  77975. cleavage
  77976. reactions@
  77977. c2-symmetry@
  77978. cacciapaglia
  77979. roberta
  77980. mandolini
  77981. luigi
  77982. specific
  77983. transition
  77984. calculating@
  77985. calixarenes
  77986. versatile
  77987. class
  77988. macrocyclic
  77989. compounds@
  77990. caluwe@
  77991. camou
  77992. capacities@
  77993. carbanion
  77994. carbanions-polar
  77995. organometal
  77996. compounds
  77997. applications
  77998. stron@
  77999. carbene
  78000. carbenes
  78001. carbenes
  78002. coordination
  78003. number
  78004. carbenes
  78005. relate@
  78006. carbeniods@
  78007. carbenoid
  78008. carbenoid
  78009. routes
  78010. substituted
  78011. phosphaalkenes
  78012. phosphabe@
  78013. carbocations
  78014. carbocyclic
  78015. compounds@
  78016. carbofunctionalizati@
  78017. carbohydrate-minor
  78018. groove
  78019. interactions
  78020. binding
  78021. carbometalation
  78022. w-dienes
  78023. olefins
  78024. catalyzed
  78025. zirco@
  78026. carbon
  78027. carbon
  78028. monoxide
  78029. carbon
  78030. component
  78031. palladium
  78032. catal@
  78033. carbonyls
  78034. carboxylic
  78035. c'n-hetero
  78036. c-1-c13
  78037. c-1027
  78038. substituted
  78039. nucleoside
  78040. analogs
  78041. c-alkylations
  78042. c-anions
  78043. c-aryl
  78044. c-arylglycoside
  78045. c-atom
  78046. c-azido
  78047. c-azido
  78048. compounds
  78049. c-azidohydrazones
  78050. c-bond
  78051. c-fused
  78052. c-glycoside
  78053. c-glycoside
  78054. synthesis
  78055. palladium-mediated
  78056. glycal-aglycon
  78057. c-glycosides
  78058. c-glycosyl
  78059. insertions
  78060. reactions
  78061. fischer
  78062. carbene
  78063. complexes
  78064. c-h-c
  78065. c-h/co/olefins
  78066. c-main
  78067. c-metallation
  78068. c-n/c-c
  78069. c-nitroso
  78070. c-nucleophiles
  78071. c-o-b
  78072. c-o-z
  78073. c-phosphorylation
  78074. c-ring
  78075. c1-c-9
  78076. c17-c22
  78077. quassinoids
  78078. total
  78079. synthesis
  78080. dl-samaderin
  78081. mmetry
  78082. asymmetric
  78083. induction
  78084. symmetric
  78085. aziridines
  78086. class
  78087. chiral
  78088. ligands
  78089. c2-symmetric
  78090. c2-symmetric
  78091. cationic
  78092. copper
  78093. complexes
  78094. chiral
  78095. lewis
  78096. c3se2
  78097. buckminsterfullerene
  78098. buckminsterfullerene
  78099. celestial
  78100. sphere
  78101. c8-epimer
  78102. cabaleiro
  78103. cacchi
  78104. cacciapaglia
  78105. cacciapaglia
  78106. mandolini
  78107. catalysis
  78108. metal
  78109. reacti
  78110. cacciapaglia
  78111. roberta
  78112. mandolini
  78113. luigi
  78114. specific
  78115. transition
  78116. cadby
  78117. cadmium
  78118. cadmium-lead
  78119. cadogan
  78120. cadogan
  78121. deoxygenation
  78122. phosphorus
  78123. reagents
  78124. cadogan
  78125. types
  78126. organophosphorus
  78127. reagents
  78128. their
  78129. cadogen
  78130. cadogen
  78131. mechanistic
  78132. radicals
  78133. hydrocarbons
  78134. caged
  78135. cages
  78136. caglioti
  78137. caine
  78138. caine
  78139. alkylation
  78140. related
  78141. reactions
  78142. ketones
  78143. cainelli
  78144. cainelli
  78145. cardillo
  78146. aspects
  78147. stereospecific
  78148. cairns
  78149. calabar
  78150. calabrese
  78151. calamenene
  78152. calanolides
  78153. calciferols
  78154. calcitriol
  78155. calcium
  78156. calculated
  78157. calculating
  78158. calculation
  78159. calculations
  78160. calderon
  78161. calderon
  78162. lawrence
  78163. ofstead
  78164. olefin
  78165. metathesis
  78166. 197817
  78167. caldwell
  78168. caldwell
  78169. creed
  78170. exciplex
  78171. intermediates
  78172. photocycl
  78173. calicenes
  78174. calicheamicin
  78175. calicheamicin
  78176. rationally
  78177. designed
  78178. molecule
  78179. extremely
  78180. calicheamicin-dna
  78181. calicheamicin/espera
  78182. calicheamicinone
  78183. calicheamicins
  78184. calicheamycin
  78185. californiaP
  78186. calix
  78187. calix
  78188. arenes
  78189. bridged
  78190. upper
  78191. calixarene
  78192. calixarene
  78193. catalyzed
  78194. generation
  78195. dichlorocarbene
  78196. calixarenes
  78197. calixarenes
  78198. versatile
  78199. class
  78200. macrocyclic
  78201. compounds
  78202. calixarenes
  78203. third
  78204. supramolecular
  78205. calixarenes
  78206. chemical
  78207. chameleons
  78208. calixarenes
  78209. paradoxes
  78210. paradigms
  78211. molecular
  78212. baskets
  78213. calixarenes
  78214. third
  78215. ation
  78216. supramolecules
  78217. calixarenes-supramol
  78218. calixarenes-supramol
  78219. pursuits
  78220. callahan
  78221. called
  78222. calphostin
  78223. caluwe
  78224. heteroannelation
  78225. aminoaldehydes
  78226. calyculin
  78227. camacho
  78228. camalli
  78229. cambie
  78230. cambie
  78231. richard
  78232. rutledge
  78233. peter
  78234. woodgate
  78235. synthetic
  78236. cambie
  78237. richard
  78238. rutledge
  78239. peter
  78240. woodgate
  78241. transforma
  78242. cambridgeK
  78243. camedo
  78244. cameoI
  78245. camilleri
  78246. camilleri
  78247. patrick
  78248. biasi
  78249. andrew
  78250. resolving
  78251. caminade
  78252. caminade
  78253. marie
  78254. majoral
  78255. pierre
  78256. mathieu
  78257. synthes
  78258. camou
  78259. camou
  78260. camoutsis
  78261. campaigne
  78262. campbell
  78263. campbell
  78264. johnson
  78265. chloramine
  78266. related
  78267. halogeno
  78268. campbell
  78269. sainsbury
  78270. searle
  78271. biosynthesis
  78272. camphor
  78273. camphor
  78274. derivatives
  78275. chiral
  78276. auxiliaries
  78277. asymmetric
  78278. campora
  78279. campora
  78280. paneque
  78281. poveda
  78282. carmona
  78283. organonickel
  78284. chemis
  78285. campos
  78286. camptothecin
  78287. camptothecin
  78288. chemistry
  78289. biogenesis
  78290. medicinal
  78291. chemistry
  78292. canal
  78293. canales
  78294. canceill
  78295. cancer
  78296. candida
  78297. candidiasis
  78298. stereochemistry
  78299. allylic
  78300. phosphate
  78301. metab
  78302. canfarini
  78303. cannabinoids
  78304. cannabis
  78305. cannizzaro
  78306. canthin
  78307. canty
  78308. canty
  78309. allan
  78310. development
  78311. organopalladium
  78312. chemistry
  78313. canudas
  78314. capabilities
  78315. capable
  78316. capacities
  78317. capacity
  78318. capillary
  78319. caplar
  78320. caplar
  78321. comisso
  78322. sunjic
  78323. homogeneous
  78324. asymmetric
  78325. hydrogenati
  78326. capnellanes
  78327. capon
  78328. capon
  78329. ghosh
  78330. grieve
  78331. direct
  78332. observation
  78333. simpl
  78334. capozzi
  78335. capozzi
  78336. lucchini
  78337. modena
  78338. thiirenium
  78339. capped
  78340. cappedophanes
  78341. capraro
  78342. capricious
  78343. capsicum
  78344. capto
  78345. capto
  78346. dative
  78347. substitution
  78348. effect
  78349. captodative
  78350. captodative
  78351. substituent
  78352. effects
  78353. radical
  78354. chemistry
  78355. capture
  78356. carba
  78357. carba-sugars
  78358. carbacephalosporins
  78359. carbalkoxycarbenes
  78360. carbamate
  78361. carbamates
  78362. carbamatoacrylates
  78363. carbamide
  78364. carbamoyl
  78365. carbamoyloxy
  78366. carbamyl
  78367. carbanion
  78368. carbanion
  78369. carbanion
  78370. accelerated
  78371. vinylcyclopropane
  78372. rearrangement
  78373. carbanion
  78374. hybridization
  78375. thiophosphonamide-st
  78376. anions
  78377. remar
  78378. carbanionen
  78379. carbanionen
  78380. methoden
  78381. organischen
  78382. chemie
  78383. carbanionic
  78384. carbanions
  78385. carbanions
  78386. alkali
  78387. alkaline
  78388. cations
  78389. selectivi
  78390. carbanions
  78391. alkali
  78392. alkaline
  78393. earth
  78394. cations
  78395. synthesis
  78396. carbanions-polar
  78397. carbanions-polar
  78398. organometal
  78399. compounds
  78400. applications
  78401. stron
  78402. carbanions-polar
  78403. organometal
  78404. compounds
  78405. metal
  78406. effects
  78407. carbanyl
  78408. carbanyl
  78409. coupling
  78410. reactions
  78411. using
  78412. valent
  78413. titanium
  78414. carbapenam
  78415. carbapenem
  78416. carbapenems
  78417. carbarhates
  78418. carbazole{
  78419. carbazole
  78420. alkaloids
  78421. carbazole
  78422. synthesis
  78423. trapping
  78424. strategy
  78425. carbazoles
  78426. carben
  78427. carbene
  78428. carbene
  78429. carbene
  78430. carbene
  78431. interconversion
  78432. between
  78433. phenyl
  78434. carbene
  78435. chemistry
  78436. carbene
  78437. complexes
  78438. catalysis
  78439. carbene
  78440. complexes
  78441. organic
  78442. synthesis
  78443. carbene
  78444. complexes
  78445. stereoselective
  78446. cycloaddition
  78447. reactions
  78448. carbene
  78449. complexes
  78450. chromium
  78451. hearing
  78452. nitrogen
  78453. substituents
  78454. carbene
  78455. methods
  78456. introduction
  78457. acylmethyl
  78458. carbene
  78459. radical
  78460. cations
  78461. carbene
  78462. reaction
  78463. heteroatoms
  78464. generate
  78465. ylides
  78466. revie
  78467. carbene
  78468. reactions
  78469. diazoesters
  78470. sigma-bonds
  78471. carbene
  78472. rearrangements
  78473. carbene
  78474. rearrangements
  78475. constrai
  78476. carbene
  78477. synthesis
  78478. chemical
  78479. reactions
  78480. 3-cyclopropeneca
  78481. carbene-c-atom
  78482. carbenegs
  78483. carbenes
  78484. carbenes
  78485. carbenes
  78486. carbenoids
  78487. neighboring
  78488. heteroatoms
  78489. carbenes
  78490. carboranes
  78491. carbenes
  78492. nitrenes
  78493. heterocyclic
  78494. chemistry
  78495. intramolecul
  78496. carbenes
  78497. carbenes
  78498. norbornenylidenes
  78499. carbenes
  78500. carbenes
  78501. carbenoids
  78502. introduction
  78503. carbenes
  78504. carbides
  78505. carbon
  78506. years
  78507. transition
  78508. metal-a
  78509. carbenes
  78510. matrixes
  78511. spectroscopy
  78512. structure
  78513. reactivity
  78514. carbenes
  78515. coordination
  78516. cycloalkenylidenes
  78517. carbenes
  78518. coordination
  78519. number
  78520. alkylidene
  78521. 1-alkenyliden
  78522. carbenes
  78523. coordination
  78524. number
  78525. carbenes
  78526. relate
  78527. carbenes
  78528. coordination
  78529. number
  78530. carbenes
  78531. carbenes
  78532. coordination
  78533. number
  78534. carbenes
  78535. containing
  78536. carbenes
  78537. coordination
  78538. number
  78539. carbenes
  78540. unsaturate
  78541. carbenes
  78542. coordination
  78543. number
  78544. cycloalkenyl
  78545. carbenes
  78546. carbenes
  78547. coordination
  78548. number
  78549. cycloalkenylidene
  78550. carben
  78551. carbenes
  78552. coordination
  78553. number
  78554. cycloalkylidenes
  78555. carbenes
  78556. coordination
  78557. number
  78558. cyclobutyl
  78559. cyclopentyl
  78560. carbenes
  78561. coordination
  78562. number
  78563. cyclopropyl
  78564. carbenes
  78565. carbenes
  78566. coordination
  78567. number
  78568. heterocycloalkyliden
  78569. carbenes
  78570. coordination
  78571. number
  78572. methylene
  78573. alkyl
  78574. carbenic
  78575. carbenic
  78576. reactivity
  78577. revisited
  78578. carbenic
  78579. selectivity
  78580. cyclopropanation
  78581. reactions
  78582. carbenium
  78583. carbenoid
  78584. carbenoid
  78585. routes
  78586. substituted
  78587. phosphaalkenes
  78588. phosphabe
  78589. carbenoid
  78590. versus
  78591. vinylogous
  78592. reactivity
  78593. rhodium
  78594. stabili
  78595. carbenoid
  78596. versus
  78597. vinylogous
  78598. reactivity
  78599. rhodium
  78600. stabilized
  78601. carbenoids
  78602. carbides
  78603. carbidocarbonyl
  78604. carbinols
  78605. carbinyl
  78606. carbo
  78607. carbo/metallocuprati
  78608. carboalumination
  78609. carboamination
  78610. carboaziridines
  78611. carbocation
  78612. carbocationic
  78613. carbocationic
  78614. related
  78615. processes
  78616. reactions
  78617. alpha-ke
  78618. carbocations
  78619. carbocations
  78620. carbocations
  78621. carbocation
  78622. radicals
  78623. carbocations
  78624. destabilized
  78625. electron-withdrawing
  78626. groups
  78627. carbocations
  78628. h-organometal
  78629. compounds
  78630. carbocupration
  78631. carbocupration
  78632. acetylenic
  78633. acetals
  78634. ketals
  78635. synthesis
  78636. carbocycle
  78637. carbocycle
  78638. construction
  78639. terpene
  78640. synthesis
  78641. carbocycles
  78642. carbocycles
  78643. carbohydrates
  78644. annulated
  78645. sugar
  78646. approach
  78647. carbocyclicp
  78648. compounds
  78649. carbocyclization
  78650. carbocyclization
  78651. acetylenic
  78652. propargylic
  78653. reagents
  78654. carbocyclizations
  78655. carbodications
  78656. carbodiimide
  78657. carbodiimides
  78658. carboethoxy
  78659. carboethoxy
  78660. carbene
  78661. laser
  78662. flash
  78663. photolysis
  78664. study
  78665. carbofunctionalizati
  78666. carbofunctionalizati
  78667. alkenes
  78668. carbofunctionalizati
  78669. alkenes
  78670. intramolecular
  78671. cycloa
  78672. carbogenic
  78673. carbohalogenation
  78674. carbohyd
  78675. carbohydrate
  78676. carbohydrate
  78677. cyclic
  78678. acetal
  78679. formation
  78680. migration
  78681. carbohydrate
  78682. dienophiles
  78683. cycloadditions
  78684. carbohydrate
  78685. thiazoles
  78686. carbohydrate-chemist
  78687. carbohydrate-minor
  78688. carbohydrate-minor
  78689. groove
  78690. interactions
  78691. binding
  78692. carbohydrates
  78693. carbohydrates
  78694. chiral
  78695. auxiliaries
  78696. stereoselective
  78697. synth
  78698. carbohydrates
  78699. chiral
  78700. templates
  78701. reoselective
  78702. carbohydrates
  78703. tandem
  78704. sharpless
  78705. dihydroxylation
  78706. enzyme
  78707. carbohydrates
  78708. chemistry
  78709. monosaccharides
  78710. their
  78711. oligomers
  78712. carbohydrates
  78713. synthetic
  78714. methods
  78715. applications
  78716. medicina
  78717. carbohyrates
  78718. carboline
  78719. carbolines
  78720. carbolithiation
  78721. carbomagnesation
  78722. carbometalation
  78723. carbometalation
  78724. addition
  78725. organometallic
  78726. compounds
  78727. carbometalation
  78728. w-dienes
  78729. olefins
  78730. catalyzed
  78731. zirco
  78732. carbometallation
  78733. carbometallation
  78734. c-metallation
  78735. alkynes
  78736. stereospecific
  78737. carbometallation
  78738. alkenes
  78739. alkynes
  78740. carbometallation-car
  78741. carbomethoxy
  78742. carbomethoxypyridini
  78743. carbonW
  78744. carbon
  78745. carbon
  78746. carbon
  78747. alkaloid
  78748. chemistry
  78749. review
  78750. carbon
  78751. routes
  78752. nitrenes
  78753. carbon
  78754. carbon
  78755. alkylations
  78756. amines
  78757. ammonium
  78758. salts
  78759. carbon
  78760. carbon
  78761. cleavage
  78762. haller
  78763. bauer
  78764. related
  78765. carbon
  78766. carbon
  78767. formation
  78768. palladium
  78769. catalyzed
  78770. intra
  78771. carbon
  78772. carbon
  78773. forming
  78774. reactions
  78775. organo
  78776. samarium
  78777. carbon
  78778. dioxide
  78779. activation
  78780. metal
  78781. complexes
  78782. carbon
  78783. disulphide
  78784. organic
  78785. chemistry
  78786. carbon
  78787. electrophiles
  78788. dienes
  78789. polyenes
  78790. promoted
  78791. carbon
  78792. hydrogen
  78793. transition
  78794. metal
  78795. bonds
  78796. carbon
  78797. clusters
  78798. carbon
  78799. monoxide
  78800. carbon
  78801. component
  78802. palladium
  78803. catal
  78804. carbon
  78805. nucleophiles
  78806. alkenes
  78807. alkynes
  78808. carbon
  78809. suboxide
  78810. derivatives
  78811. carbon
  78812. suboxide
  78813. preparative
  78814. organic
  78815. chemistry
  78816. carbon
  78817. sulfur
  78818. cleavages
  78819. substituted
  78820. aminomethyl
  78821. carbon-boron
  78822. carbon-c
  78823. carbon-c
  78824. cleavage
  78825. haller-bauer
  78826. related
  78827. carbon-carbonF
  78828. carbon-carbon
  78829. alkylations
  78830. amines
  78831. ammonium
  78832. salts
  78833. carbon-carbon
  78834. carbon-hydrogen
  78835. activation
  78836. ditungs
  78837. formation
  78838. addition
  78839. carbenium
  78840. carbon-carbon
  78841. formation
  78842. insertion
  78843. carbon-carbon
  78844. formation
  78845. means
  78846. zirconocene-derived
  78847. carbon-carbon
  78848. formation
  78849. electron-deficient
  78850. aromatic
  78851. carbon-carbon
  78852. formation
  78853. heterocycles
  78854. using
  78855. nickel
  78856. carbon-carbon
  78857. formation
  78858. involving
  78859. boron
  78860. reagents
  78861. carbon-carbon
  78862. formation
  78863. carbonyl-car
  78864. complexes
  78865. carbon-carbon
  78866. formation
  78867. hypervalent
  78868. iodine
  78869. oxidatio
  78870. carbon-carbon
  78871. forming
  78872. reactions
  78873. organotransition
  78874. carbon-centered
  78875. carbon-centered
  78876. radicals
  78877. amino
  78878. acids
  78879. their
  78880. derivati
  78881. carbon-element
  78882. carbon-fluorine
  78883. carbon-fulleranes
  78884. carbon-halogen
  78885. carbon-heteroatom
  78886. carbon-hydrogen
  78887. n-hydrogen
  78888. activation
  78889. organometallics
  78890. carbon-metal
  78891. carbon-nitrogen
  78892. carbon-oxygen
  78893. carbon-oxygen
  78894. activation
  78895. transition
  78896. metal
  78897. complexes
  78898. carbon-phosphorus
  78899. carbon-selenium
  78900. carbon-silicon
  78901. carbon-silicon
  78902. carbon-substitution
  78903. carbon-substitution
  78904. nitrogen
  78905. heterocycles
  78906. carbon-sulfur
  78907. carbonate
  78908. carbonates
  78909. carbonic
  78910. carbonic
  78911. derivatives
  78912. general
  78913. introduction
  78914. carbonitrile
  78915. carbonium
  78916. carbonium
  78917. penta
  78918. hexacoordinated
  78919. cations
  78920. carbonolide
  78921. carbonphosphorus
  78922. carbons
  78923. carbonyl
  78924. carbonyl
  78925. carbonyl
  78926. addition
  78927. reactions
  78928. promoted
  78929. cerium
  78930. reagents
  78931. carbonyl
  78932. compounds
  78933. alpha-cleavage
  78934. carbonyl
  78935. compounds
  78936. cycloaddition
  78937. carbonyl
  78938. derivatives
  78939. titanium
  78940. zirconium
  78941. hafnium
  78942. carbonyl
  78943. group
  78944. derivatization
  78945. carbonyl
  78946. group
  78947. regeneration
  78948. substantive
  78949. enhancement
  78950. carbonyl-car
  78951. carbonyl-compounds
  78952. carbonyl-coupling
  78953. carbonyl-coupling
  78954. reactions
  78955. using
  78956. low-valent
  78957. titanium
  78958. carbonyl-ene
  78959. carbonyl-promoted
  78960. carbonyl-tethered
  78961. carbonylalkyl
  78962. carbonylation
  78963. decarbonylation
  78964. reactions
  78965. carbonylation
  78966. direct
  78967. carbonyl
  78968. compounds
  78969. carbonylation
  78970. tertiary
  78971. propargylic
  78972. alcohols
  78973. catalyzed
  78974. carbonylation
  78975. zirconocene
  78976. complexes
  78977. carbonylations
  78978. carbonylative
  78979. carbonylcarbenes
  78980. carbonylcarbenes
  78981. specific
  78982. synthesis
  78983. natural
  78984. produc
  78985. carbonylchromium
  78986. carbonylchromium
  78987. complexes
  78988. organic
  78989. synthesis
  78990. carbonylhydrazones
  78991. carbonyliron
  78992. carbonylmethylene
  78993. carbonyls
  78994. carbonyls
  78995. carbonyls/reppe
  78996. carbooxygenation
  78997. carbopalladation
  78998. carborane
  78999. carboranes
  79000. carboranyl
  79001. carboranylcarbenes
  79002. carboranylcarbenes
  79003. dehydrocarboranes
  79004. carbovirs
  79005. carboxaldehydes
  79006. carboxamidates
  79007. carboxamide
  79008. carboxamides
  79009. carboxy
  79010. carboxyanhydrides
  79011. carboxyl
  79012. carboxylate
  79013. carboxylates
  79014. carboxylation
  79015. carboxylato
  79016. carboxyli
  79017. carboxyli
  79018. amino
  79019. esters
  79020. o-acyl
  79021. hydroxylamines
  79022. carboxylic
  79023. carboxylic
  79024. carboxylic
  79025. chlorides
  79026. carboxylic
  79027. esters
  79028. carboxylic
  79029. salts
  79030. carboxylic
  79031. acids
  79032. carboxylic
  79033. acids
  79034. carboxylic
  79035. derivatives
  79036. general
  79037. carboxylic
  79038. amides
  79039. their
  79040. n-derivatives
  79041. carboxylic
  79042. anhydrides
  79043. carboxymethyl
  79044. carboxymethylation
  79045. carboxyolefination
  79046. carbozincation
  79047. carbyne
  79048. carbyne
  79049. complexes
  79050. carbynes
  79051. carcanague
  79052. carcinogenic
  79053. carcinogenicity
  79054. cardillo
  79055. cardiotoxic
  79056. cardodiimide
  79057. carelessness
  79058. carey
  79059. carey
  79060. resolutions
  79061. design
  79062. chemistry
  79063. britai
  79064. carless
  79065. carless
  79066. howard
  79067. cyclohexa
  79068. diene
  79069. diols
  79070. carlo
  79071. carlos
  79072. carlsen
  79073. carlson
  79074. carlson
  79075. design
  79076. optimization
  79077. organic
  79078. synthesis
  79079. carlson
  79080. nordahl
  79081. exploring
  79082. organic
  79083. synthetic
  79084. experim
  79085. carmack
  79086. carmely
  79087. carmen
  79088. carmichael
  79089. carmona
  79090. carnahan
  79091. carnahan
  79092. edmund
  79093. protasiewicz
  79094. lippard
  79095. stephen
  79096. enoids
  79097. polyterpenoids
  79098. carole
  79099. caroline
  79100. carolyn
  79101. carotenoid
  79102. carotenoids
  79103. carotenoids-selected
  79104. carpenter
  79105. carpino
  79106. carpyrinic
  79107. carraher
  79108. carreira
  79109. carrier
  79110. carriers
  79111. carrnely
  79112. carrupt
  79113. carruthers
  79114. carless
  79115. howard
  79116. cyclohexa
  79117. diene
  79118. diols
  79119. carruthers
  79120. modern
  79121. methods
  79122. organic
  79123. synthesis
  79124. camb@
  79125. cascade
  79126. cyclization
  79127. synthesis
  79128. tuberine@
  79129. cassiol
  79130. catalysis
  79131. catalysts@
  79132. catalyszed@
  79133. asymmetric
  79134. hydrogen
  79135. migration
  79136. allylamines
  79137. catalytic
  79138. carbonylations
  79139. nitrogen
  79140. containing
  79141. organic
  79142. comp@
  79143. catalytic
  79144. hydrogenation
  79145. organic
  79146. synthesis@
  79147. catalytic
  79148. ring-closing
  79149. metathasis
  79150. powerful
  79151. technique
  79152. catalyzed
  79153. catenands
  79154. cationic
  79155. zirconium
  79156. catalysts
  79157. carbon
  79158. carbon
  79159. forming
  79160. caubere
  79161. unimetal
  79162. super
  79163. bases
  79164. chemical
  79165. reviews
  79166. centenary@
  79167. cerium
  79168. amide
  79169. enolate
  79170. addition
  79171. aldehydes
  79172. ketones@
  79173. chain
  79174. challenges
  79175. change
  79176. characterization
  79177. nonrigid
  79178. behaviour
  79179. carboxylate
  79180. charney
  79181. chelation
  79182. chemical
  79183. carruthers
  79184. modern
  79185. methods
  79186. organic
  79187. synthesis
  79188. carsten
  79189. carter
  79190. caruso
  79191. caruthers
  79192. caruthers
  79193. marvin
  79194. chemical
  79195. synthesis
  79196. analogs
  79197. carvalho
  79198. carvone
  79199. caryoynencins
  79200. casadevall
  79201. casalnuovo
  79202. casanova
  79203. casbene
  79204. cascade
  79205. synthesis
  79206. tuberine
  79207. cascade
  79208. cyclizations
  79209. cascades
  79210. casen
  79211. casensky
  79212. cases
  79213. casey
  79214. casey
  79215. metal
  79216. carbene
  79217. complexes
  79218. reactive
  79219. intermediat
  79220. casey
  79221. charles
  79222. organorhenium
  79223. chemistry
  79224. science
  79225. washington
  79226. cason
  79227. caspar
  79228. caspi
  79229. caspi
  79230. biosynthesis
  79231. tetrahymanol
  79232. tetrahymena
  79233. pyriform
  79234. cassar
  79235. cassels
  79236. cassels
  79237. shamma
  79238. stereostructure
  79239. specific
  79240. rotation
  79241. cassiol
  79242. cassiol
  79243. castaldi
  79244. castanospermine
  79245. castasterone
  79246. castedo
  79247. castle
  79248. castro
  79249. castulik
  79250. steric
  79251. factor
  79252. medicinal
  79253. chemistry
  79254. dissymm
  79255. cat6alyzed
  79256. organic
  79257. reactions
  79258. inorganic
  79259. solids
  79260. catafusenes
  79261. catal
  79262. cataly
  79263. catalylic
  79264. catalylic
  79265. hydrogenation
  79266. esters
  79267. alcohols
  79268. homer
  79269. adkins
  79270. catalysed
  79271. catalysed
  79272. addition
  79273. aldehydes
  79274. activated
  79275. double
  79276. bonds
  79277. catalysist
  79278. catalysis
  79279. catalysis
  79280. catalysis
  79281. lithium
  79282. perchlorate
  79283. diethyl
  79284. ether
  79285. intramolec
  79286. catalysis
  79287. metal
  79288. compleses
  79289. metal
  79290. promoted
  79291. selectivi
  79292. catalysis
  79293. metal
  79294. reactions
  79295. crown
  79296. ether
  79297. substrat
  79298. catalysis
  79299. two-phase
  79300. systems
  79301. phase
  79302. transfer
  79303. related
  79304. catalysis
  79305. organic
  79306. reactions
  79307. inorganic
  79308. solids
  79309. catalysis
  79310. claisen
  79311. rearrangements
  79312. catalystH
  79313. catalysts
  79314. lyszed
  79315. catalyt
  79316. catalyticv
  79317. catalytic
  79318. lective
  79319. oxida
  79320. catalytic
  79321. aldol
  79322. reactions
  79323. application
  79324. catalytic
  79325. efficient
  79326. allylic
  79327. tertiary
  79328. benzylic
  79329. catalytic
  79330. antibodies
  79331. catalytic
  79332. antibodies
  79333. mechanistic
  79334. practical
  79335. consideration
  79336. catalytic
  79337. antibodies--designer
  79338. enzymes
  79339. catalytic
  79340. applications
  79341. transition
  79342. metals
  79343. organic
  79344. synth
  79345. catalytic
  79346. applications
  79347. transition-metal
  79348. complexes
  79349. catalytic
  79350. asymmetric
  79351. aldol
  79352. reaction
  79353. chiral
  79354. enolate
  79355. catalytic
  79356. asymmetric
  79357. allylation
  79358. reactions
  79359. enantios
  79360. catalytic
  79361. asymmetric
  79362. allylation
  79363. aldehydes
  79364. catalytic
  79365. asymmetric
  79366. allylation
  79367. using
  79368. chiral
  79369. acyloxy
  79370. boran
  79371. catalytic
  79372. asymmetric
  79373. arylation
  79374. olefins
  79375. catalytic
  79376. asymmetric
  79377. benzylation
  79378. achiral
  79379. lithium
  79380. enolates
  79381. catalytic
  79382. asymmetric
  79383. carbonyl
  79384. reactions
  79385. catalytic
  79386. asymmetric
  79387. cyanohydrin
  79388. synthesis
  79389. catalytic
  79390. asymmetric
  79391. diels
  79392. alder
  79393. reactions
  79394. catalytic
  79395. asymmetric
  79396. diels
  79397. alder
  79398. reactions
  79399. pyrone
  79400. deriv
  79401. catalytic
  79402. asymmetric
  79403. diels-alder
  79404. reactions
  79405. catalytic
  79406. asymmetric
  79407. dihydroxylation
  79408. catalytic
  79409. asymmetric
  79410. dihydroxylation
  79411. tetrasubstituted
  79412. catalytic
  79413. asymmetric
  79414. hydrogen
  79415. migration
  79416. allylamines
  79417. catalytic
  79418. asymmetric
  79419. hydrogen
  79420. migration
  79421. allylamines
  79422. catalytic
  79423. asymmetric
  79424. induction
  79425. enantioselective
  79426. conjugate
  79427. catalytic
  79428. asymmetric
  79429. michael
  79430. reactions
  79431. promoted
  79432. lithium
  79433. catalytic
  79434. asymmetric
  79435. nitroaldol
  79436. reaction
  79437. using
  79438. optically
  79439. catalytic
  79440. asymmetric
  79441. reduction
  79442. allylic
  79443. esters
  79444. formic
  79445. catalytic
  79446. asymmetric
  79447. synthesis
  79448. catalytic
  79449. asymmetric
  79450. synthesis
  79451. means
  79452. secondary
  79453. interac
  79454. catalytic
  79455. asymmetric
  79456. synthesis
  79457. cyclopropanecarboxyl
  79458. acids
  79459. catalytic
  79460. asymmetric
  79461. synthesis
  79462. axially
  79463. chiral
  79464. biaryls
  79465. catalytic
  79466. asymmetric
  79467. synthesis
  79468. benzylic
  79469. quaternary
  79470. carbon
  79471. catalytic
  79472. asymmetric
  79473. synthesis
  79474. either
  79475. enantiomer
  79476. physo
  79477. catalytic
  79478. asymmetric
  79479. synthesis
  79480. homoallylic
  79481. alcohols
  79482. catalytic
  79483. asymmetric
  79484. synthesis
  79485. optically
  79486. active
  79487. alcohols
  79488. catalytic
  79489. asymmetric
  79490. synthesis
  79491. trans
  79492. chelating
  79493. chiral
  79494. catalytic
  79495. olefin
  79496. coupling
  79497. catalytic
  79498. carbonylations
  79499. nitrogen
  79500. containing
  79501. organic
  79502. catalytic
  79503. chemistry
  79504. technology
  79505. carbon
  79506. compounds
  79507. catalytic
  79508. conversion
  79509. paraffinic
  79510. hydrocarbons
  79511. isopara
  79512. catalytic
  79513. decomposition
  79514. diazomethane
  79515. general
  79516. method
  79517. catalytic
  79518. decomposition
  79519. organic
  79520. organoelemental
  79521. perox
  79522. catalytic
  79523. diastereoselective
  79524. synthesis
  79525. cis-12-disubstitut
  79526. catalytic
  79527. eactions
  79528. formation
  79529. reactions
  79530. hydrocarbona
  79531. catalytic
  79532. enantioselective
  79533. aldol
  79534. additions
  79535. methyl
  79536. catalytic
  79537. enantioselective
  79538. coupling
  79539. allyl
  79540. transfer
  79541. catalytic
  79542. enantioselective
  79543. coupling
  79544. allyl
  79545. transfer
  79546. catalytic
  79547. enantioselective
  79548. inverse
  79549. electron
  79550. demand
  79551. diels
  79552. catalytic
  79553. enantioselective
  79554. synthesis
  79555. dihydropyrones
  79556. catalytic
  79557. epoxidation
  79558. molecular
  79559. oxygen
  79560. using
  79561. nickel
  79562. catalytic
  79563. hydrogenation
  79564. carbon
  79565. atoms
  79566. catalytic
  79567. hydrogenation
  79568. hetero
  79569. atoms
  79570. catalytic
  79571. hydrogenation
  79572. organic
  79573. synthesis
  79574. catalytic
  79575. hydrogenation
  79576. esters
  79577. alcohols
  79578. catalytic
  79579. hydrosilation
  79580. organic
  79581. esters
  79582. using
  79583. manganese
  79584. alkoxy
  79585. furanones
  79586. catalytic
  79587. methods
  79588. metal
  79589. carbene
  79590. transformations
  79591. catalytic
  79592. oxidation
  79593. secondary
  79594. amines
  79595. tetra
  79596. propyla
  79597. catalytic
  79598. oxidations
  79599. hydrogen
  79600. peroxide
  79601. oxidant
  79602. catalytic
  79603. reactions
  79604. carbohalogenation
  79605. carbooxygenation
  79606. catalytic
  79607. reactions
  79608. elimination
  79609. catalytic
  79610. reactions
  79611. hydrogenation
  79612. hydrometallation
  79613. dimet
  79614. catalytic
  79615. reactions
  79616. hydrooxygenation
  79617. hydrosulfonation
  79618. catalytic
  79619. reactions
  79620. isomerizations
  79621. rearrangements
  79622. catalytic
  79623. reactions
  79624. metathesis
  79625. cometathesis
  79626. catalytic
  79627. reactions
  79628. oxidative
  79629. reactions
  79630. catalytic
  79631. reactions
  79632. reductive
  79633. substitutions
  79634. catalytic
  79635. reduction
  79636. aromatic
  79637. hydrocarbons
  79638. catalytic
  79639. closing
  79640. metathesis
  79641. powerful
  79642. technique
  79643. catalytic
  79644. ring-closing
  79645. metathasis
  79646. powerful
  79647. technique
  79648. catalytic
  79649. semihydrogenation
  79650. triple
  79651. catalytic
  79652. synthesis
  79653. organic
  79654. compounds
  79655. carbonylation
  79656. catalytic
  79657. synthesis
  79658. sulfides
  79659. sulfoxides
  79660. sulfones
  79661. catalytic
  79662. synthesis
  79663. thiophene
  79664. alkylthiophenes
  79665. catalytic
  79666. tandem
  79667. oxy-palladation
  79668. vinylation
  79669. catalytic
  79670. transfer
  79671. hydrogenation
  79672. catalytic
  79673. versatility
  79674. nickel
  79675. function
  79676. prepara
  79677. catalytical
  79678. catalyttc
  79679. catalyze
  79680. catalyzedG
  79681. catalyzed
  79682. catalyzed
  79683. catalyzed
  79684. chiral
  79685. molybdenum
  79686. alkylidene
  79687. complex
  79688. catechol
  79689. catecholborane
  79690. catecholborane
  79691. hydroboration
  79692. reagent
  79693. catechols
  79694. catellani
  79695. catenands
  79696. catenands
  79697. catenates
  79698. caterpillar
  79699. catha
  79700. catharanthus
  79701. catharonthus
  79702. catherine
  79703. cathodic
  79704. cathodic
  79705. reduction
  79706. nitro
  79707. compounds
  79708. cathy
  79709. cation
  79710. cation
  79711. radical
  79712. cycloaddition
  79713. related
  79714. sigmatropic
  79715. reactio
  79716. cation
  79717. radical
  79718. cycloadditions
  79719. related
  79720. sigmatropic
  79721. reacti
  79722. cation
  79723. radical
  79724. probes
  79725. development
  79726. application
  79727. matallo
  79728. cation-radical
  79729. cation-radical
  79730. pericyclic
  79731. reactions
  79732. cation-stabilizing
  79733. cationic
  79734. cationic
  79735. cyclizations
  79736. iminium
  79737. their
  79738. sigmatrop
  79739. cationic
  79740. zirconium
  79741. catalysts
  79742. carbon
  79743. carbon
  79744. forming
  79745. cations
  79746. cations
  79747. strained
  79748. polycyclic
  79749. compounds
  79750. caton
  79751. catriona
  79752. catslysis
  79753. catsoulacos
  79754. catsoulacos
  79755. catsoulacos
  79756. formation
  79757. steroids
  79758. catsoulacos
  79759. catsoulacos
  79760. synthesis
  79761. pyrido
  79762. caubere
  79763. caubere
  79764. complex
  79765. bases
  79766. complex
  79767. reducing
  79768. agents
  79769. caubere
  79770. unimetal
  79771. super
  79772. bases
  79773. chemical
  79774. reviews
  79775. cauci
  79776. caulfield
  79777. caulton
  79778. causing
  79779. cavaleiro
  79780. cavallo
  79781. cavell
  79782. cavell
  79783. metal
  79784. chelate
  79785. systems
  79786. catalysts
  79787. olefin
  79788. cavill
  79789. cavities
  79790. cavity
  79791. cavity-shaped
  79792. cbi-tmi
  79793. cbi-tmi
  79794. synthesis
  79795. evaluation
  79796. analog
  79797. cc-1065
  79798. ccuring
  79799. cebulak
  79800. cecilia
  79801. cecl3
  79802. ceclia
  79803. celebi
  79804. celebrates
  79805. celestial
  79806. cell-wall
  79807. cells
  79808. cellular
  79809. cembran
  79810. cembran
  79811. pseudopteranoids
  79812. cubitanoids
  79813. natural
  79814. cembranes
  79815. cembranoid
  79816. cembranoids
  79817. cembrene
  79818. centenary
  79819. centennial
  79820. center
  79821. centered
  79822. centers
  79823. central
  79824. centre
  79825. centred
  79826. centres
  79827. century
  79828. cephalosporin}
  79829. cephalosporins
  79830. cephalostatin
  79831. cephalotasus
  79832. cephalotaxine
  79833. cephalotaxus
  79834. cephamycin
  79835. cephamycins
  79836. cephem
  79837. cephems
  79838. ceric
  79839. ceric
  79840. oxidation
  79841. organic
  79842. chemistry
  79843. cerioalkoxide
  79844. cerium
  79845. cerium
  79846. amide
  79847. enolate
  79848. addition
  79849. aldehydes
  79850. ketones
  79851. cerium
  79852. chloride
  79853. facilitates
  79854. formation
  79855. ketones
  79856. cerium
  79857. chloride
  79858. promoted
  79859. nucleophilic
  79860. addition
  79861. organo
  79862. cerny
  79863. certain
  79864. cerveau
  79865. cerveny
  79866. cesium
  79867. cesium
  79868. fluoride
  79869. promoted
  79870. cyclization
  79871. synthesis
  79872. cesium
  79873. effect
  79874. macrocyclization
  79875. cesium
  79876. effect
  79877. macrocyclization
  79878. critical
  79879. review
  79880. cetal
  79881. cetylenic
  79882. cetylpyridinium
  79883. cevane
  79884. cf3c2cf3
  79885. cf3coo
  79886. cf3sime3
  79887. interaction
  79888. implic
  79889. tions
  79890. organic
  79891. chemistry
  79892. mical
  79893. modifications
  79894. sugars
  79895. inhibitors
  79896. n-glycopr
  79897. ch-ch
  79898. ch-co
  79899. ch2c12
  79900. ch2c6h5
  79901. chaabouni
  79902. chaerkasov
  79903. chain
  79904. chain
  79905. chained
  79906. chains}
  79907. chair-chair
  79908. chair-chair
  79909. interconversions
  79910. six-membered
  79911. rings
  79912. chakrabartty
  79913. chakrabartty
  79914. alkaline
  79915. hypohalite
  79916. oxidations
  79917. oxidation
  79918. chakraborty
  79919. chakraborty
  79920. carbazole
  79921. alkaloids
  79922. progress
  79923. chakraborty
  79924. chemistry
  79925. biology
  79926. carbazole
  79927. alkaloids
  79928. chakraborty
  79929. shyamali
  79930. carbazole
  79931. alkaloids
  79932. chalcogen
  79933. chalcogen-containing
  79934. chalcogenide
  79935. chalcogenides
  79936. chalcogenonium
  79937. chalcogens
  79938. chalcone
  79939. chalcones
  79940. chalk
  79941. challandp
  79942. challenge
  79943. challenges
  79944. challenges
  79945. chaloner
  79946. chaloner
  79947. penny
  79948. homogeneous
  79949. hydrogenation
  79950. catalysis
  79951. chamberlin
  79952. chambers
  79953. chambers
  79954. sargent
  79955. polyfluoroheteroarom
  79956. compounds
  79957. chambers
  79958. jensen
  79959. stereochemistry
  79960. bromine
  79961. chambron
  79962. chambron
  79963. claude
  79964. dietrich
  79965. buchecker
  79966. christiane
  79967. sauvage
  79968. chameleon
  79969. chameleons
  79970. champagne
  79971. fleming
  79972. electrophilic
  79973. substitution
  79974. organosilic
  79975. chemistry
  79976. allene
  79977. oxides
  79978. chiral
  79979. organosilicon
  79980. compounds
  79981. asymmetric
  79982. chance
  79983. chand
  79984. chandra
  79985. chandrasekaram
  79986. chandrasekaran
  79987. chandrasekhar
  79988. chandrasekhar
  79989. vadapalli
  79990. muralidhara
  79991. madaligar
  79992. gopalakrishna
  79993. chandross
  79994. chanet
  79995. chang
  79996. chang
  79997. clifford
  79998. marine
  79999. isocyano
  80000. compounds
  80001. topics
  80002. curre
  80003. change
  80004. change
  80005. changes
  80006. channels
  80007. chanon
  80008. chanon
  80009. michel
  80010. variety
  80011. molecular
  80012. schemes
  80013. border
  80014. chapdelaine
  80015. chapel
  80016. chapman
  80017. chapman
  80018. practical
  80019. organic
  80020. spectrometry
  80021. wiley
  80022. chapter
  80023. character
  80024. characterisation
  80025. characteristic
  80026. characteristic
  80027. reduction
  80028. ketones
  80029. bu3snh-bu4nx
  80030. system
  80031. characteristics
  80032. characteristics
  80033. reactions
  80034. allyl
  80035. their
  80036. characteristics
  80037. hypercoordinate
  80038. silicon
  80039. compounds
  80040. characterization
  80041. characterization
  80042. nonrigid
  80043. behaviour
  80044. carboxylate
  80045. characterization
  80046. chemical
  80047. physical
  80048. methods
  80049. characterizations
  80050. characterized
  80051. charcoal
  80052. charette
  80053. charette
  80054. andre
  80055. mellon
  80056. christophe
  80057. rouillard
  80058. langis
  80059. malenfan
  80060. charge
  80061. charge
  80062. component
  80063. reaction
  80064. design
  80065. invention
  80066. charge
  80067. reaction
  80068. design
  80069. cationic
  80070. cyclizations
  80071. charge-accelerated
  80072. charge-accelerated
  80073. rearrangements
  80074. charge-transfer
  80075. charge-transfer
  80076. complexes
  80077. organosilicon
  80078. compounds
  80079. charged
  80080. charles
  80081. charlton
  80082. charney
  80083. charney
  80084. charney
  80085. molecular
  80086. basis
  80087. optical
  80088. activity
  80089. wiley
  80090. charpentier
  80091. charton
  80092. charton
  80093. electrical
  80094. effect
  80095. substituent
  80096. constants
  80097. correl
  80098. charushin
  80099. chatgilialoglu
  80100. chatgilialoglu
  80101. chryssostomos
  80102. organosilanes
  80103. radical
  80104. based
  80105. chattopadhyaya
  80106. chaussard
  80107. chauvette
  80108. chauzov
  80109. chava
  80110. chch2n
  80111. reactions
  80112. newly
  80113. available
  80114. pyridines
  80115. cheeseman
  80116. cheeseman
  80117. cookson
  80118. condensed
  80119. pyrazine
  80120. chemistry
  80121. cheeseman
  80122. werstiuk
  80123. quinoxaline
  80124. chemistry
  80125. develop
  80126. cheikh
  80127. chela
  80128. chela
  80129. flores
  80130. julian
  80131. comments
  80132. novel
  80133. approach
  80134. chelain
  80135. chelalion
  80136. chelate
  80137. chelate
  80138. controlled
  80139. diastereoselective
  80140. addition
  80141. epoxy
  80142. chelates
  80143. chelating
  80144. chelation
  80145. chelation
  80146. chelation
  80147. assistance
  80148. activation
  80149. csp3-s
  80150. bonds
  80151. chelation
  80152. controlled
  80153. chemo
  80154. regio
  80155. enantio
  80156. selective
  80157. synth
  80158. chelation
  80159. non-chelation
  80160. control
  80161. addition
  80162. reactions
  80163. chelation-controlled
  80164. chelation-controlled
  80165. addition
  80166. dialkylzincs
  80167. trans-a
  80168. cheletropic
  80169. chelsea
  80170. chemk
  80171. synthesis
  80172. oligosaccharides
  80173. related
  80174. chem1992
  80175. chemi
  80176. chemica
  80177. chemicals
  80178. chemical
  80179. chemical
  80180. chemical
  80181. chemical
  80182. analysis
  80183. polycyclic
  80184. aromatic
  80185. compounds
  80186. chemical
  80187. chemical
  80188. biochemical
  80189. manipulations
  80190. nucieic
  80191. acids@
  80192. chemically
  80193. chemie
  80194. chemistry
  80195. chemistry
  80196. biology
  80197. carbazole
  80198. alkaloids@
  80199. chemistry
  80200. alicyclic
  80201. compounds
  80202. structure
  80203. chemical
  80204. tran@
  80205. chemistry
  80206. ethanediyl
  80207. acetals
  80208. stereoselective
  80209. synt@
  80210. chemistry
  80211. pseudo-sugar@
  80212. chemo@
  80213. chemoenzymatic@
  80214. meldrum's
  80215. organic
  80216. synthesis
  80217. chichester
  80218. chimiques
  80219. chiral
  80220. nitrogen
  80221. heterocycles
  80222. ligands
  80223. chirality
  80224. molecular
  80225. recognition
  80226. air-water
  80227. interfa@
  80228. chiusoli
  80229. salerno
  80230. synthetic
  80231. application
  80232. organonickel@
  80233. chloroarenes@
  80234. chemical
  80235. chemical
  80236. chemical
  80237. chemical
  80238. chemical
  80239. analysis
  80240. polycyclic
  80241. aromatic
  80242. compounds
  80243. chemical
  80244. chemical
  80245. biochemical
  80246. manipulations
  80247. nucieic
  80248. acids
  80249. chemical
  80250. biolog
  80251. synthesis
  80252. chiral
  80253. epoxides
  80254. chemical
  80255. biological
  80256. aspects
  80257. polyether-ionophore
  80258. antib
  80259. chemical
  80260. biological
  80261. synthesis
  80262. chiral
  80263. epoxides
  80264. chemical
  80265. structural
  80266. comparison
  80267. n-boc-cbq
  80268. n-boc-cb
  80269. chemical
  80270. emulation
  80271. biosynthetic
  80272. route
  80273. glycinoelepi
  80274. chemical
  80275. modification
  80276. biopolymers
  80277. quinones
  80278. quino
  80279. chemical
  80280. multiplication
  80281. chirality
  80282. science
  80283. application
  80284. chemical
  80285. properties
  80286. triketones
  80287. reexamination
  80288. albizat
  80289. chemical
  80290. reaction
  80291. molten
  80292. salts
  80293. their
  80294. reactions
  80295. chemical
  80296. relaxation
  80297. methods
  80298. organic
  80299. chemistry
  80300. chemical
  80301. synthesis
  80302. analogs
  80303. chemical
  80304. synthesis
  80305. glycosphingolipids
  80306. chemical
  80307. synthesis
  80308. heparin
  80309. fragments
  80310. analogues
  80311. chemical
  80312. transformations
  80313. disproportionation
  80314. sulfur
  80315. chemically
  80316. chemically
  80317. chemically
  80318. modified
  80319. polymers
  80320. chemicals
  80321. chemicaltransformati
  80322. chemie
  80323. chemie
  80324. chemigtry
  80325. chemiluminescence
  80326. chemiluminescences
  80327. chemist
  80328. chemist's
  80329. chemistr
  80330. chemistries
  80331. chemistryJ
  80332. chemistry
  80333. chemistry
  80334. chemistry
  80335. chemistry
  80336. chemistry
  80337. chemistry
  80338. chemistry
  80339. chemistry
  80340. chemistry
  80341. chemistry
  80342. chemistry
  80343. chemistry
  80344. chemistry
  80345. chemistry
  80346. chemistry
  80347. chemistry
  80348. azole
  80349. alkaloids
  80350. chemistry
  80351. biology
  80352. enediyne
  80353. anticancer
  80354. antibiotics
  80355. chemistry
  80356. biology
  80357. n-nitroso
  80358. compounds
  80359. chemistry
  80360. biology
  80361. naturally
  80362. occurring
  80363. acetylenes
  80364. chemistry
  80365. biology
  80366. taxol
  80367. chemistry
  80368. biology
  80369. immunosuppressant
  80370. fk-506
  80371. chemistry
  80372. crystal
  80373. growth
  80374. chemistry
  80375. developments
  80376. fluorinated
  80377. carbohydrates
  80378. chemistry
  80379. structure
  80380. elucidation
  80381. kedarcidin
  80382. chromo
  80383. chemistry
  80384. synthetic
  80385. utility
  80386. cobalt-complexed
  80387. propargy
  80388. chemistry
  80389. diplatinum
  80390. centers
  80391. chemistry
  80392. 3-membered
  80393. carbon-phosphorus
  80394. heterocycles
  80395. chemistry
  80396. 3.1.0
  80397. bicyclohexanes
  80398. analogs
  80399. chemistry
  80400. benzotriazol
  80401. alkylpyridines
  80402. unusual
  80403. chemistry
  80404. alicyclic
  80405. compounds
  80406. structure
  80407. chemical
  80408. chemistry
  80409. allene
  80410. episulfides
  80411. thiiranoradialenes
  80412. chemistry
  80413. allene
  80414. oxides
  80415. chemistry
  80416. alpha-cyanothioaceta
  80417. chemistry
  80418. highly
  80419. reactive
  80420. metals
  80421. chemistry
  80422. antitumour
  80423. agents
  80424. chemistry
  80425. benzo
  80426. thiophene-23-dione
  80427. chemistry
  80428. c-azidohydrazones
  80429. elopments
  80430. perspectives
  80431. chemistry
  80432. carba-sugars
  80433. pseudo-sugars
  80434. their
  80435. derivative
  80436. chemistry
  80437. carbenes
  80438. l-sized
  80439. cyclic
  80440. compounds
  80441. chemistry
  80442. carbonyl
  80443. oxides
  80444. generated
  80445. ozonolysis
  80446. chemistry
  80447. cationic
  80448. dicyclopentadie
  80449. group
  80450. metal-alkyl
  80451. chemistry
  80452. chlorocarbonyl
  80453. isocyanate
  80454. chemistry
  80455. cyclopropanone
  80456. hemiacetals
  80457. their
  80458. applicatio
  80459. chemistry
  80460. cyclopropenones
  80461. chemistry
  80462. diazabicycloundecene
  80463. other
  80464. pyrimidoazep
  80465. chemistry
  80466. diazirines
  80467. chemistry
  80468. enoxysilacyclobutane
  80469. highly
  80470. selective
  80471. uncatalyz
  80472. chemistry
  80473. ethanediyl
  80474. acetals
  80475. stereoselective
  80476. chemistry
  80477. extradiol
  80478. aromatic
  80479. cleavage
  80480. isolation
  80481. chemistry
  80482. galloyl-derived
  80483. o-quinones
  80484. reactivity
  80485. toward
  80486. chemistry
  80487. heterocyclic
  80488. diazo
  80489. compounds
  80490. chemistry
  80491. lactam
  80492. acetals
  80493. chemistry
  80494. multifunctional
  80495. carbon
  80496. compounds
  80497. synthetic
  80498. chemistry
  80499. methoxy
  80500. methylamides
  80501. applications
  80502. synthe
  80503. chemistry
  80504. n-methoxy-n-methylam
  80505. applications
  80506. synthesis
  80507. chemistry
  80508. nucleosides
  80509. nucleotides
  80510. chemistry
  80511. organo-zirconium
  80512. hafnium
  80513. compounds
  80514. chemistry
  80515. organochromium
  80516. complexes
  80517. chemistry
  80518. organosulfur
  80519. compounds
  80520. general
  80521. problems
  80522. chemistry
  80523. oxaziridines
  80524. asymmetric
  80525. oxidations
  80526. using
  80527. hetero
  80528. chemistry
  80529. oxaziridines
  80530. synthesis
  80531. reactions
  80532. chiral
  80533. chemistry
  80534. phosphonium
  80535. salts
  80536. containing
  80537. systems
  80538. chemistry
  80539. phosphorylcarbenes
  80540. chemistry
  80541. potentially
  80542. prebiological
  80543. natural
  80544. products
  80545. chemistry
  80546. pseudo-sugar
  80547. chemistry
  80548. pyrazoles
  80549. condensed
  80550. heteroaromatic
  80551. chemistry
  80552. rotational
  80553. isomers
  80554. chemistry
  80555. spiro
  80556. ketals
  80557. spiro
  80558. review
  80559. chemistry
  80560. spiroacetals
  80561. chemistry
  80562. spiroketals
  80563. chemistry
  80564. stable
  80565. alpha-halogeno-organ
  80566. compounds
  80567. chemistry
  80568. cyclopentadienyl
  80569. bisphosphine
  80570. ruthenium
  80571. chemistry
  80572. polyhedral
  80573. boron
  80574. halides
  80575. diboron
  80576. chemistry
  80577. thiacyclobutenes
  80578. thietes
  80579. their
  80580. valence
  80581. chemistry
  80582. titanocene
  80583. zirconocene
  80584. chemistry
  80585. trialkylsilyl
  80586. perfluoralkane
  80587. sulfonates
  80588. chemistry
  80589. viologens
  80590. chemistry
  80591. ylids
  80592. survey
  80593. progress
  80594. chemistry
  80595. chemistry
  80596. damage
  80597. repair
  80598. thymine
  80599. thymidine
  80600. chemistry
  80601. without
  80602. borders
  80603. betwee
  80604. group
  80605. transition
  80606. chemistry/bioscience
  80607. chemistryof
  80608. chemists
  80609. chemlstry
  80610. chemo
  80611. enzymatic
  80612. chemoenzymatic
  80613. synthesis
  80614. amino
  80615. acids
  80616. derivatives
  80617. chemoenzymic
  80618. chemoreception
  80619. chemoselective
  80620. chemoselective
  80621. nucleophilic
  80622. attack
  80623. dicyano
  80624. epoxides
  80625. chemoselectivity
  80626. chemoselectivity
  80627. chromium
  80628. mediated
  80629. synthesis
  80630. chemoselectivity
  80631. organometallic
  80632. reactions
  80633. appraisa
  80634. chemoselectivity
  80635. organometallic
  80636. reactions
  80637. using
  80638. principle
  80639. chemosensors
  80640. chemosystematics
  80641. chemotactic
  80642. chemotaxonomy
  80643. chemotheraphy
  80644. chemsitry
  80645. chemtech
  80646. chemtracts
  80647. chemyshev
  80648. chenR
  80649. meldrum's
  80650. organic
  80651. synthesis
  80652. jianxin
  80653. scheffer
  80654. trotter
  80655. james
  80656. differences
  80657. chenchaiah
  80658. chenet
  80659. chengS
  80660. cheng
  80661. methanol
  80662. production
  80663. chemistryS
  80664. chengji
  80665. chenier
  80666. chenier
  80667. favorskii
  80668. rearrangement
  80669. bridged
  80670. polycyclic
  80671. chensheng
  80672. cherkashin
  80673. cherkasov
  80674. cherkasova
  80675. chernoivanov
  80676. chernokal'skii
  80677. chernov
  80678. chernyshev
  80679. cherry
  80680. cheves
  80681. chevolot
  80682. chevolot
  80683. guanidine
  80684. derivatives
  80685. marine
  80686. natural
  80687. products
  80688. chiang
  80689. chiang
  80690. yvonne
  80691. kresge
  80692. jerry
  80693. enols
  80694. other
  80695. reactive
  80696. specie
  80697. chiba
  80698. chibata
  80699. chichesterL
  80700. chichester
  80701. chichibabin
  80702. chida
  80703. chihairo
  80704. childs
  80705. childs
  80706. photochemistry
  80707. protonated
  80708. unsaturated
  80709. childs
  80710. ronald
  80711. photochemistry
  80712. carbenium
  80713. chilton
  80714. chimia
  80715. chimiak
  80716. chimica
  80717. chimie
  80718. chimique
  80719. chimiques
  80720. chimiques
  80721. chimirri
  80722. chimirri
  80723. gitto
  80724. rosaria
  80725. grasso
  80726. silvana
  80727. monforte
  80728. banaszczyk
  80729. jubian
  80730. mrejen
  80731. artificial
  80732. chinese
  80733. chini
  80734. chinnasamy
  80735. chira
  80736. chirals
  80737. chiral
  80738. chiral
  80739. chiral
  80740. acetals
  80741. enantio
  80742. diastereoselective
  80743. substitutio
  80744. chiral
  80745. acyclic
  80746. nitrone
  80747. bearing
  80748. protected
  80749. vicinal
  80750. contro
  80751. chiral
  80752. alkoxyallylic
  80753. allenic
  80754. stannanes
  80755. reagents
  80756. chiral
  80757. amides
  80758. asymmetric
  80759. synthesis
  80760. chiral
  80761. arene
  80762. chromium
  80763. carbonyl
  80764. complexes
  80765. asymmetric
  80766. synth
  80767. chiral
  80768. auxiliary
  80769. directed
  80770. asymmetric
  80771. nucleophile
  80772. additions
  80773. chiral
  80774. aziridination
  80775. alkenes
  80776. chiral
  80777. aziridines
  80778. review
  80779. chiral
  80780. aziridines
  80781. their
  80782. synthesis
  80783. stereoselective
  80784. chiral
  80785. building
  80786. blocks
  80787. based
  80788. technical
  80789. grade
  80790. citronellene
  80791. chiral
  80792. building
  80793. blocks
  80794. enantiomer
  80795. synthesis
  80796. sugars
  80797. chiral
  80798. building
  80799. blocks
  80800. enantiomer
  80801. synthesis
  80802. using
  80803. enzymat
  80804. chiral
  80805. carboxylic
  80806. acids
  80807. chiral
  80808. catalysts
  80809. enantioselective
  80810. carbenoid
  80811. cyclopropana
  80812. chiral
  80813. compounds
  80814. synthesised
  80815. biocatalytic
  80816. reductions
  80817. chiral
  80818. cyclic
  80819. amidines
  80820. chiral
  80821. dipole
  80822. stabilized
  80823. anions
  80824. stereoselective
  80825. deprotonatio
  80826. chiral
  80827. discriminations
  80828. cinchona
  80829. alkaloids
  80830. chiral
  80831. eta6-arene
  80832. chromium
  80833. complexes
  80834. organic
  80835. synthesis
  80836. chiral
  80837. arene
  80838. chromium
  80839. complexes
  80840. organic
  80841. synthesis
  80842. chiral
  80843. inductio
  80844. using
  80845. heterocycles
  80846. chiral
  80847. induction
  80848. using
  80849. heterocycles
  80850. chiral
  80851. lanthanide
  80852. compounds
  80853. chiral
  80854. lanthanide
  80855. shift
  80856. reagents
  80857. chiral
  80858. lewis
  80859. acids
  80860. catalytic
  80861. asymmetric
  80862. reactions
  80863. chiral
  80864. ligands
  80865. based
  80866. pyridine
  80867. framework
  80868. synthesis
  80869. chiral
  80870. ligands
  80871. asymmetric
  80872. catalysis
  80873. chiral
  80874. lithium-1-oxyalkanid
  80875. asymmetric
  80876. deprotonation
  80877. chiral
  80878. methyl
  80879. groups
  80880. small
  80881. beautiful
  80882. chiral
  80883. mobile
  80884. phases
  80885. enantiomeric
  80886. analysis
  80887. chiral
  80888. molecules
  80889. chiral
  80890. nitro
  80891. olefins
  80892. enantioselective
  80893. reactions
  80894. chiral
  80895. non-racemic
  80896. bicyclic
  80897. lactams
  80898. vehicles
  80899. constru
  80900. synthesis
  80901. chiral
  80902. organosulfur
  80903. compounds
  80904. chiral
  80905. reagents
  80906. asymmetric
  80907. constructi
  80908. carbon
  80909. framew
  80910. chiral
  80911. semicorrins
  80912. nitrogen
  80913. heterocycles
  80914. ligands
  80915. chiral
  80916. semicorrins
  80917. related
  80918. nitrogen
  80919. heterocycles
  80920. chiral
  80921. separations
  80922. chiral
  80923. sulfinylallyl
  80924. alpha
  80925. sulfinyl
  80926. ketimine
  80927. anions
  80928. chiral
  80929. sulfinylallyl
  80930. alpha-sulfinyl
  80931. ketimine
  80932. anions
  80933. chiral
  80934. synthesis
  80935. benzo
  80936. quinolizidine-type
  80937. apangium
  80938. chiral
  80939. synthesis
  80940. organoboranes
  80941. remarkably
  80942. rapid
  80943. chiral
  80944. synthesis
  80945. organoboranes
  80946. racemic
  80947. diastereo
  80948. chiral
  80949. synthons
  80950. ester
  80951. hydrolysis
  80952. catalyzed
  80953. liver
  80954. chiral
  80955. synthons
  80956. enzyme-mediated
  80957. asymmetrization
  80958. meso-
  80959. chirality
  80960. chirality
  80961. protec
  80962. chirality
  80963. molecular
  80964. recognition
  80965. air-water
  80966. interfa
  80967. chirality
  80968. bosons
  80969. alpha-helix
  80970. chirality
  80971. alpha
  80972. beta-adrenoceptor
  80973. agonists
  80974. antago
  80975. chirality
  80976. carbonium
  80977. carbanions
  80978. radicals
  80979. chirality
  80980. design
  80981. synthesis
  80982. chirality
  80983. industry
  80984. commercial
  80985. manufacture
  80986. applica
  80987. chirality
  80988. organic
  80989. synthesis
  80990. biocatalysts
  80991. chirality
  80992. preservation
  80993. cation
  80994. radical
  80995. intermediate
  80996. chirality
  80997. transfer
  80998. sigmatropic
  80999. rearrangements
  81000. chirally
  81001. chirbase
  81002. chiro
  81003. chiron
  81004. chirons
  81005. chiroptical
  81006. chirospecific
  81007. chirospecific
  81008. synthesis
  81009. 1-amino-3
  81010. hydroxymethyl
  81011. chirotechnology
  81012. chirotechnology
  81013. industrial
  81014. synthesis
  81015. optically
  81016. active
  81017. chisholm
  81018. chistokletov
  81019. chistovalova
  81020. chitin
  81021. chiusoli
  81022. chiusoli
  81023. salerno
  81024. synthetic
  81025. application
  81026. organonickel
  81027. chizhov
  81028. chkanikov
  81029. chlenov
  81030. chloral
  81031. chloramine
  81032. chloramine
  81033. related
  81034. n-halogeno-n-metallo
  81035. reagents
  81036. chloramines
  81037. chloride
  81038. chloride-mediated
  81039. chlorides
  81040. chlorinated
  81041. chlorination
  81042. chlorinations
  81043. chlorine
  81044. chloro
  81045. chloro
  81046. olefin
  81047. annelation
  81048. chloroacetamide
  81049. chloroacetates
  81050. chloroacetophenone
  81051. chloroacetylenes
  81052. chloroalkenylamines
  81053. chloroalkyl
  81054. chloroarenes
  81055. chlorobenzo
  81056. chlorobutanoic
  81057. chlorocarbonates
  81058. chlorocarbonyl
  81059. chlorochromate
  81060. chlorocyclo
  81061. chlorocyclophosphaze
  81062. chloroformates
  81063. chloromethyl
  81064. chloromethylation
  81065. chloromethylation
  81066. aromatic
  81067. compounds
  81068. chloromethylation
  81069. aromatic
  81070. compounds
  81071. reynold
  81072. fuson
  81073. chloromethyltrimethy
  81074. chloroperbenzoic
  81075. chlorophenyl
  81076. chlorophyll
  81077. chloroprene
  81078. chloropropeniminium
  81079. chlorosilyl
  81080. chlorosulfenyl
  81081. chlorosulfides
  81082. chlorosulfonyl
  81083. chlorosulfonyl
  81084. isocyanate
  81085. novel
  81086. reagent
  81087. synthesis
  81088. chlorosulfonyl
  81089. isocyanate
  81090. synthetic
  81091. reagent
  81092. chlorosulfonyl
  81093. isocyanate
  81094. silver
  81095. anniversary
  81096. lively
  81097. chlorosulfonylcarbam
  81098. chlorosulfonylisocya
  81099. chlorosulphonyl
  81100. chlorothio
  81101. chlorothricolide
  81102. chlorotrimethyl
  81103. chlorotrimethyl
  81104. silyl
  81105. accelerated
  81106. conjugate
  81107. addition
  81108. chlorotrimethylsilan
  81109. chlorotrimethylsilan
  81110. acetonitrile
  81111. system
  81112. promoter
  81113. chlorotropic
  81114. chlorotropic
  81115. rearrangements
  81116. sulfanyl
  81117. sulfonylalkan
  81118. chlral
  81119. chmielewski
  81120. chobanyan
  81121. choice
  81122. chojnowski
  81123. cholaphanes
  81124. cholaphaneset
  81125. cholesterol
  81126. sterols
  81127. choline
  81128. choon
  81129. choose
  81130. chorev
  81131. chorismic
  81132. heteroaromatic
  81133. ortho
  81134. quinodimethanes
  81135. review
  81136. choudhary
  81137. choussy
  81138. aminium
  81139. radicals
  81140. reactive
  81141. intermediates
  81142. danen
  81143. nelsen
  81144. rosenblatt
  81145. nonaromatic
  81146. chowdhury
  81147. chris
  81148. christe
  81149. christensen
  81150. chlorotrimethyl
  81151. silyl
  81152. accelerated
  81153. conjugate
  81154. addition
  81155. orga@
  81156. cholesterols@
  81157. christenson@
  81158. chromatography
  81159. chromium-catalyzed
  81160. oxidations
  81161. organic
  81162. synthesis@
  81163. chromophore-derived@
  81164. cilento
  81165. trans
  81166. isomerisation
  81167. alkenes@
  81168. cis-12-disubstituted@
  81169. claisen
  81170. rearrangements
  81171. heteroaromatic
  81172. systems@
  81173. clive
  81174. selenium
  81175. reagents
  81176. organic
  81177. synthesis
  81178. closo@
  81179. cobalt-complexed@
  81180. cocatalyzed@
  81181. collet
  81182. brienne
  81183. jacques
  81184. optical
  81185. resolution
  81186. direct
  81187. colonna
  81188. combinations@
  81189. comisso
  81190. compendium
  81191. complex@
  81192. complex
  81193. eliminations
  81194. eliminations
  81195. rearrangements@
  81196. complexes
  81197. complexes
  81198. containing
  81199. heteronuclear
  81200. metal
  81201. metal
  81202. complexes
  81203. carboxylic
  81204. acids
  81205. pyridines
  81206. pyridine
  81207. compounds
  81208. christenson
  81209. christer
  81210. christian
  81211. christiane
  81212. christides
  81213. christine
  81214. christl
  81215. christl
  81216. benzvalene
  81217. properties
  81218. synthetic
  81219. potential
  81220. christoph
  81221. christophe
  81222. christopher
  81223. christopherson
  81224. chroman
  81225. chromanols
  81226. chromanols
  81227. chromanones
  81228. chromones
  81229. chromanone
  81230. chromanones
  81231. chromans
  81232. chromatoQ
  81233. chromatogr
  81234. chromatographic
  81235. chromatographic
  81236. enantioseparation
  81237. methods
  81238. applications
  81239. chromatographically
  81240. chromatographyQ
  81241. chromatography
  81242. chromen
  81243. chromene
  81244. chromenes
  81245. chromenone
  81246. chromium
  81247. chromium
  81248. carbene
  81249. complexes
  81250. organic
  81251. synthesis
  81252. recent
  81253. devel
  81254. chromium
  81255. carbene
  81256. complexes
  81257. synthesis
  81258. molecules
  81259. chromium
  81260. directed
  81261. regio
  81262. stereocontrol
  81263. chapter
  81264. chromium
  81265. based
  81266. methods
  81267. carbon
  81268. carbon
  81269. formation
  81270. chromium
  81271. mediated
  81272. nickel
  81273. catalyzed
  81274. cylclisations
  81275. chromium
  81276. mediated
  81277. stereodivergent
  81278. additions
  81279. allylic
  81280. chromium
  81281. molybdenum
  81282. tungsten
  81283. annual
  81284. survey
  81285. covering
  81286. chromium-catalyzed
  81287. chromium-catalyzed
  81288. oxidations
  81289. organic
  81290. synthesis
  81291. chromocarcerands
  81292. chromogenic
  81293. chromone
  81294. chromones
  81295. chromophor
  81296. chromophore
  81297. -derived
  81298. chromophores
  81299. chromophorically
  81300. chrysanthemic
  81301. chryssostomos
  81302. chrzastek
  81303. chudek
  81304. chugaev
  81305. chuit
  81306. chuit
  81307. claude
  81308. corriu
  81309. robertj
  81310. catherine
  81311. young
  81312. colin
  81313. chukovskaya
  81314. chuman
  81315. chung
  81316. chupakhin
  81317. chupakhin
  81318. alekseev
  81319. rudakov
  81320. charushin
  81321. recent
  81322. advances
  81323. churms
  81324. chuvatkin
  81325. chvalovsky
  81326. chvertkina
  81327. chvertkina
  81328. khoklov
  81329. mironov
  81330. phosphorus
  81331. derivative
  81332. cumambulatory
  81333. rearrangements
  81334. cicchi
  81335. cidep
  81336. cidnp
  81337. ciganek
  81338. ciguatoxin
  81339. cilente
  81340. cilento
  81341. cilento
  81342. cimarusti
  81343. cimino
  81344. cimino
  81345. guido
  81346. sodano
  81347. guido
  81348. biosynthesis
  81349. secondary
  81350. metaboli
  81351. cinchona
  81352. cinnamic
  81353. cinnamoyl
  81354. cinnamyl
  81355. cinnolines
  81356. cintas
  81357. cintas
  81358. activated
  81359. metals
  81360. organic
  81361. synthesis
  81362. press
  81363. cintas
  81364. asymmetric
  81365. synthesis
  81366. alpha
  81367. amino
  81368. acids
  81369. cintas
  81370. pedro
  81371. addition
  81372. organochromium
  81373. compounds
  81374. aldehyd
  81375. cioslowski
  81376. evidence
  81377. complex
  81378. reaction
  81379. pathway
  81380. circular
  81381. circulene
  81382. circumabulatory
  81383. circumabulatory
  81384. rearrangements
  81385. circumambulatory
  81386. circumstellar
  81387. cirrincione
  81388. epoxides
  81389. sharpless
  81390. asymmetric
  81391. dihydroxylation
  81392. reacti
  81393. trans
  81394. isomerisation
  81395. alkenes
  81396. trans
  81397. isomerization
  81398. immines
  81399. cis-12-dialkenylcycl
  81400. cis-2
  81401. cis-cyclohexene-12-d
  81402. cis-diols
  81403. cis-olefins
  81404. cis-substituted
  81405. cistone
  81406. citronellene
  81407. citterio
  81408. ciufolini
  81409. claesson
  81410. clair
  81411. claisen
  81412. claisen
  81413. rearrangeme
  81414. heteroaromatic
  81415. systems
  81416. claisen
  81417. rearrangement
  81418. alkyl
  81419. ethers
  81420. prepared
  81421. claisen
  81422. rearrangement
  81423. phosphates
  81424. claisen
  81425. rearrangement
  81426. silyl
  81427. ketene
  81428. acetals
  81429. generate
  81430. claisen
  81431. rearrangements
  81432. clar's
  81433. claramunt
  81434. claramunt
  81435. maria
  81436. elguero
  81437. chemistry
  81438. pyrazolid
  81439. clardy
  81440. clare
  81441. claremon
  81442. clarendon
  81443. claret
  81444. clarification
  81445. clarifies
  81446. clark
  81447. clark
  81448. fluoride
  81449. organic
  81450. synthesis
  81451. clark
  81452. james
  81453. kybett
  81454. adrian
  81455. macquarrie
  81456. duncan
  81457. supported
  81458. clarke
  81459. claschke
  81460. claschke
  81461. chromatographic
  81462. resolution
  81463. racemates
  81464. clasen
  81465. clasical
  81466. class
  81467. classesy
  81468. classic
  81469. classical
  81470. classical
  81471. nonclassical
  81472. methyleneboranes
  81473. classification
  81474. classification
  81475. nomenclature
  81476. peptides
  81477. their
  81478. deriva
  81479. classification
  81480. hetarenes
  81481. classification
  81482. structure
  81483. thermochemical
  81484. organic
  81485. clathrate
  81486. clathrates
  81487. claude
  81488. claude
  81489. claudel
  81490. claudel
  81491. breysse
  81492. faure
  81493. guenin
  81494. chemiluminescence
  81495. claudia
  81496. claudine
  81497. claudio
  81498. clausen
  81499. clausen
  81500. priess
  81501. christensen
  81502. joergen
  81503. synthesis
  81504. clavizepine
  81505. clavulanic
  81506. claycop
  81507. clays
  81508. clayton
  81509. cleaning
  81510. cleaning-up
  81511. cleaning-up
  81512. oxidations
  81513. hydrogen
  81514. peroxide
  81515. cleavage
  81516. ethers
  81517. cleavage
  81518. ethers
  81519. cleavage
  81520. ethers
  81521. organic
  81522. synthesis
  81523. cleavage
  81524. silicon
  81525. carbon
  81526. bonds
  81527. their
  81528. application
  81529. cleavage
  81530. reactions
  81531. cleavages
  81532. cleavers
  81533. cleaves
  81534. cleaving
  81535. clefts
  81536. clemens
  81537. clement
  81538. clement
  81539. herbert
  81540. instrumentation
  81541. clemeolide
  81542. clemmensen
  81543. clemmensen
  81544. reduction
  81545. ketones
  81546. anhydrous
  81547. organic
  81548. solvent
  81549. clennan
  81550. clennan
  81551. edward
  81552. synthetic
  81553. mechanistic
  81554. aspects
  81555. cleomeolide
  81556. cleotides
  81557. clerc
  81558. clercq
  81559. clerici
  81560. clerodane
  81561. clerodane
  81562. diterpenoids
  81563. clezy
  81564. clezy
  81565. peter
  81566. studies
  81567. porphyrin
  81568. chemistry
  81569. synthetic
  81570. cliff
  81571. clifford
  81572. cliffs
  81573. clift
  81574. clinical
  81575. clive
  81576. clive
  81577. modern
  81578. organoselenium
  81579. chemistry
  81580. clive
  81581. selenium
  81582. reagents
  81583. organic
  81584. synthesis
  81585. clock
  81586. clode
  81587. clode
  81588. carbohydrate
  81589. cyclic
  81590. acetal
  81591. formation
  81592. migration
  81593. closed
  81594. closely
  81595. closing
  81596. closure
  81597. closures
  81598. clough
  81599. clough
  81600. strobilurins
  81601. oudemansins
  81602. myxothiazols
  81603. clouthier
  81604. cluster
  81605. clusters
  81606. cmpds
  81607. cneoraceae
  81608. cntalysts
  81609. catalyzed
  81610. opening
  81611. carbonylation
  81612. cyclic
  81613. coaggregation
  81614. coarctate
  81615. coates
  81616. coatings
  81617. cobalt
  81618. cobalt
  81619. catalysed
  81620. component
  81621. coupling
  81622. involving
  81623. ketones
  81624. cobalt
  81625. catalyzed
  81626. regioselective
  81627. allylation
  81628. dicarbonyl
  81629. cobalt
  81630. mediated
  81631. total
  81632. synthesis
  81633. epoxydictymene
  81634. cobalt-catalyzed
  81635. cobalt-catalyzed
  81636. diels-alder
  81637. cobalt-complexed
  81638. cobalt-mediated
  81639. cobalt-mediated
  81640. cycloadditions
  81641. maturing
  81642. synthetic
  81643. cobalt-mediated
  81644. radical
  81645. reactions
  81646. organic
  81647. synthesis
  81648. cobalt-mediated
  81649. steroid
  81650. synthesis
  81651. cobaltcomplexed
  81652. cobaltocene
  81653. cocagne
  81654. cocarcinogenic
  81655. cocarcinogens
  81656. cocatalyst
  81657. cocatalytic
  81658. cocatalyzed
  81659. coccinine
  81660. cocivera
  81661. cockerill
  81662. cocyclization
  81663. codimerization
  81664. codon
  81665. coefficient
  81666. coelacanths
  81667. coelacanths
  81668. catalysis
  81669. coelenterates
  81670. coenzyme
  81671. coenzymes
  81672. coevolution
  81673. cofacial
  81674. cofactor
  81675. cofactors
  81676. cognac
  81677. cognition
  81678. cohalogenation
  81679. cohalogenation
  81680. organic
  81681. synthesis
  81682. cohen
  81683. cohen
  81684. benson
  81685. estimation
  81686. heats
  81687. formation
  81688. organ
  81689. coiling
  81690. coinpounds
  81691. colbalt
  81692. colchicum
  81693. coler
  81694. recent
  81695. stereoselective
  81696. synthetic
  81697. approaches
  81698. betar
  81699. coleman
  81700. coleman
  81701. jones
  81702. silenes
  81703. reviews
  81704. chemical
  81705. colin
  81706. collagen
  81707. collection
  81708. collective
  81709. collectively
  81710. colleen
  81711. collet
  81712. collet
  81713. brienne
  81714. jacques
  81715. optical
  81716. resolution
  81717. direct
  81718. collet
  81719. andre
  81720. dutasta
  81721. pierre
  81722. lozach
  81723. benedict
  81724. cryptophane
  81725. collet
  81726. andre
  81727. dutasta
  81728. pierre
  81729. lozach
  81730. benedicte
  81731. canceill
  81732. collier
  81733. collin
  81734. collin
  81735. excited
  81736. unsaturated
  81737. radicals
  81738. produced
  81739. collins
  81740. collins
  81741. sheldrake
  81742. crosby
  81743. chirality
  81744. industry
  81745. collins
  81746. djuric
  81747. stevan
  81748. synthesis
  81749. therapeutically
  81750. collins
  81751. designing
  81752. ligands
  81753. oxidizing
  81754. complexes
  81755. collman
  81756. collman
  81757. hegedus
  81758. principles
  81759. applications
  81760. organ
  81761. collman
  81762. wagenknecht
  81763. hutchinson
  81764. molecular
  81765. catalys
  81766. colloquium
  81767. collum
  81768. collum
  81769. david
  81770. tetramethylethylened
  81771. ligand
  81772. collum
  81773. david
  81774. solution
  81775. structures
  81776. lithium
  81777. dialkylamides
  81778. cologne
  81779. colombo
  81780. colombo
  81781. maria
  81782. zinczuk
  81783. ruveda
  81784. edmundo
  81785. synthetic
  81786. colomer
  81787. colone
  81788. colonna
  81789. colonna
  81790. colonna
  81791. martino
  81792. poloni
  81793. marino
  81794. alpha
  81795. effect
  81796. color
  81797. colorants
  81798. coloration
  81799. colored
  81800. colour
  81801. colquhoun
  81802. colquhoun
  81803. thompson
  81804. twigg
  81805. carbonylation
  81806. direct
  81807. colthup
  81808. columbus
  81809. colvin
  81810. colvin
  81811. silicon
  81812. organic
  81813. synthesis
  81814. chemical
  81815. colvin
  81816. silicon
  81817. organic
  81818. synthesis
  81819. butterworth
  81820. publishe
  81821. comasseto
  81822. comasseto
  81823. joaov
  81824. vinylictellurides
  81825. precursors
  81826. vinyllithium
  81827. combier
  81828. combination
  81829. natorial
  81830. combined
  81831. combined
  81832. classical
  81833. chemoenzymatic
  81834. glycosylations
  81835. combined
  81836. diphenyltin
  81837. sulfide
  81838. lawesson's
  81839. reagent
  81840. combustion
  81841. comdounds
  81842. comds
  81843. cometathesis
  81844. comformational
  81845. comined
  81846. comins
  81847. comisso
  81848. comisso
  81849. commemoration
  81850. comments
  81851. commercial
  81852. commision
  81853. commission
  81854. common
  81855. commun
  81856. communication
  81857. comounds
  81858. compactin
  81859. company
  81860. comparative
  81861. comparative
  81862. cumulene
  81863. substituent
  81864. effects
  81865. ketenes
  81866. allenes
  81867. comparative
  81868. reactivities
  81869. hydrocarbon
  81870. carbon-hydrogen
  81871. comparative
  81872. studies
  81873. generation
  81874. cyclization
  81875. reacti
  81876. comparison
  81877. comparison
  81878. group
  81879. transition
  81880. metal
  81881. chemistry
  81882. compartmentalization
  81883. compass
  81884. compd
  81885. compds
  81886. compendium
  81887. compendium
  81888. compensation
  81889. competing
  81890. competing
  81891. concepts
  81892. electronic
  81893. control
  81894. selection
  81895. competing
  81896. insertion
  81897. elimination
  81898. rhodium
  81899. carbeno
  81900. competition
  81901. competition
  81902. methods
  81903. scales
  81904. alkyl-radical
  81905. reaction
  81906. competitive
  81907. compiexes
  81908. compilation
  81909. compl
  81910. complementarity
  81911. complementary
  81912. comples
  81913. compleses
  81914. completeL
  81915. complete
  81916. reverse
  81917. regioselection
  81918. wacker
  81919. oxidation
  81920. aceto
  81921. completion
  81922. complex
  81923. rearrangements
  81924. complex
  81925. induced
  81926. proximity
  81927. effects
  81928. enantioselective
  81929. syntheses
  81930. complex
  81931. induced
  81932. proximity
  81933. effects
  81934. evidence
  81935. complex
  81936. complex
  81937. reducing
  81938. agents
  81939. novel
  81940. using
  81941. sodium
  81942. hydride
  81943. complex
  81944. reducing
  81945. agents
  81946. versatile
  81947. novel
  81948. using
  81949. complex-derived
  81950. complex-forming
  81951. complexation
  81952. complexational
  81953. complexe
  81954. complexes
  81955. complexes
  81956. complexes
  81957. complexes
  81958. complexes
  81959. carbon
  81960. monoxide
  81961. relatives
  81962. ganometa
  81963. complexes
  81964. carbon
  81965. monoxide
  81966. relatives
  81967. organometa
  81968. complexes
  81969. carboxylic
  81970. acids
  81971. pyridines
  81972. pyridine
  81973. complexes
  81974. carboxylic
  81975. acids
  81976. pyridines
  81977. pyridine
  81978. complexes
  81979. carboxylic
  81980. acids
  81981. pyridines
  81982. pyridine
  81983. complexes
  81984. metal
  81985. cations
  81986. carbohydrates
  81987. solution
  81988. complexes
  81989. substituent-free
  81990. acyclic
  81991. cyclic
  81992. phosphoru
  81993. complexex
  81994. complexing
  81995. complexity
  81996. complexones
  81997. compo
  81998. compolation
  81999. componds
  82000. component
  82001. components
  82002. composed
  82003. compositae
  82004. composition
  82005. compou
  82006. compoumds
  82007. compound
  82008. compounda
  82009. compoundsC
  82010. compounds
  82011. compounds
  82012. compounds
  82013. compounds
  82014. compounds
  82015. compounds
  82016. compounds
  82017. compounds
  82018. ounds
  82019. alkali
  82020. alkaline
  82021. earth
  82022. metals
  82023. organic
  82024. compounds
  82025. aluminium
  82026. organic
  82027. synthesis
  82028. compounds
  82029. dicoordinate
  82030. arsenic
  82031. chemical
  82032. properties
  82033. compounds
  82034. thallium
  82035. organic
  82036. synthesis
  82037. compounds
  82038. cadmium
  82039. mercury
  82040. copper
  82041. silver
  82042. compounds
  82043. silicon-silicon
  82044. germanium-germanium
  82045. tin-t
  82046. compounds
  82047. three-membered
  82048. rings
  82049. containing
  82050. boron
  82051. compounds-applicatio
  82052. compoundsnindustrial
  82053. comprehensive
  82054. comprehensive
  82055. handbook
  82056. hydrosilylation
  82057. comprehensive
  82058. organic
  82059. transformations
  82060. compressed
  82061. compression
  82062. computational
  82063. computations
  82064. computer
  82065. computer
  82066. assisted
  82067. design
  82068. chiral
  82069. boron
  82070. enolates
  82071. novel
  82072. computer
  82073. assisted
  82074. evaluation
  82075. carbene
  82076. chemistry
  82077. cameo
  82078. computers
  82079. comutational
  82080. concave
  82081. concentrated
  82082. conception
  82083. conception
  82084. birth
  82085. receptor
  82086. chemistry
  82087. dibenzo-
  82088. concepts
  82089. conceptual
  82090. concerning
  82091. concerning
  82092. diasterofacial
  82093. selectivity
  82094. aldol
  82095. react
  82096. concerning
  82097. mechanism
  82098. elimination
  82099. hypervalent
  82100. concerning
  82101. mechanism
  82102. grignard
  82103. reagent
  82104. formation
  82105. evide
  82106. concert
  82107. concerted
  82108. concerted
  82109. fragmentation
  82110. amino
  82111. decompos
  82112. concerted
  82113. mechanisms
  82114. group
  82115. transfer
  82116. reactions
  82117. concertedness
  82118. concetta
  82119. concise
  82120. synthesis
  82121. taxol
  82122. synthon
  82123. formation
  82124. concise
  82125. synthesis
  82126. perovskone
  82127. conclusion
  82128. concomitant
  82129. concomitant
  82130. epoxide
  82131. deoxygenation
  82132. deacylation
  82133. glycidy
  82134. concrete
  82135. condensates
  82136. condensation
  82137. condensation
  82138. condensations
  82139. condensed^
  82140. condensed
  82141. 124-triazines
  82142. fused
  82143. heterocycles
  82144. three
  82145. condensed
  82146. 4-thiazolidinones
  82147. condensed
  82148. pyrazines
  82149. overall
  82150. review
  82151. condition
  82152. conditionsE
  82153. tions
  82154. alkylation
  82155. ambident
  82156. anions
  82157. condomp
  82158. condon
  82159. conduction
  82160. conductive
  82161. conductivity
  82162. conductors
  82163. conduritols
  82164. confalone
  82165. conference
  82166. confertifolin
  82167. configurated
  82168. configuration
  82169. gurational
  82170. configurationally
  82171. configurations
  82172. confinement
  82173. confining
  82174. confirmation
  82175. conformationj
  82176. conformational
  82177. conformational
  82178. conformational
  82179. analysis
  82180. transition
  82181. state
  82182. asymmetr
  82183. conformational
  82184. analysis
  82185. heterocyclic
  82186. systems
  82187. recent
  82188. resul
  82189. conformational
  82190. analysis
  82191. saturated
  82192. heterocycli
  82193. compounds
  82194. conformational
  82195. analysis
  82196. 14-membered
  82197. macrolides
  82198. using
  82199. conformational
  82200. analysis
  82201. bicyclo
  82202. 3.3.1
  82203. nonanes
  82204. their
  82205. conformational
  82206. analysis
  82207. medium-sized
  82208. heterocycles
  82209. conformational
  82210. analysis
  82211. membered
  82212. sulfur
  82213. containing
  82214. conformational
  82215. analysis
  82216. six-membered
  82217. sulfur-containing
  82218. conformational
  82219. analysis
  82220. fundamental
  82221. contributions
  82222. conformational
  82223. aspects
  82224. many-member
  82225. rings
  82226. conformational
  82227. control
  82228. macrolide
  82229. synthesis
  82230. conformational
  82231. study
  82232. sncl4
  82233. complexes
  82234. aldehydes
  82235. b-uns
  82236. conformationally
  82237. b-amino
  82238. isosteres
  82239. prepared
  82240. conformationally
  82241. rigid
  82242. acyclic
  82243. 23266-tetramethyl-35
  82244. tmhdiol
  82245. conformations
  82246. conformations
  82247. conformations
  82248. five-membered
  82249. rings
  82250. confrontation
  82251. congener
  82252. congeneric
  82253. congeners
  82254. congested
  82255. congestive
  82256. conglomerate
  82257. conia
  82258. coniceine
  82259. conjugate
  82260. addition
  82261. alkyl
  82262. grignard
  82263. reagents
  82264. mononitroar
  82265. conjugate
  82266. addition
  82267. chloride
  82268. unsaturated
  82269. chiral
  82270. conjugate
  82271. addition
  82272. reactio
  82273. organic
  82274. synthesis
  82275. conjugate
  82276. addition
  82277. reactions
  82278. organocopper
  82279. reagents
  82280. conjugate
  82281. addition
  82282. reactions
  82283. organocopper
  82284. reagents
  82285. conjugate
  82286. additions
  82287. carbon
  82288. ligands
  82289. activated
  82290. alkenes
  82291. conjugate
  82292. additions
  82293. reactive
  82294. carbanions
  82295. activated
  82296. conjugatedG
  82297. conjugated
  82298. enediynes-an
  82299. topic
  82300. different
  82301. light
  82302. conjugated
  82303. nitroalkenes
  82304. versatile
  82305. intermediates
  82306. organic
  82307. conjugation
  82308. conjugation-extended
  82309. conjugation-extended
  82310. assemblies
  82311. central
  82312. heterocycl
  82313. conjunction
  82314. connected
  82315. connection
  82316. connections
  82317. connectivities
  82318. connelly
  82319. connie
  82320. connollyW
  82321. connolly
  82322. ngadjui
  82323. triterpenoids
  82324. natural
  82325. connolly
  82326. triterpenoids
  82327. second
  82328. supplements
  82329. connolly
  82330. organic
  82331. compounds
  82332. divalent
  82333. conocurvone
  82334. conocurvone
  82335. prototype
  82336. class
  82337. anti-hiv
  82338. active
  82339. conquest
  82340. conrad
  82341. conrad
  82342. dissection
  82343. heparin
  82344. future
  82345. conrapolarization
  82346. conrapolarization
  82347. concept
  82348. organic
  82349. reactivity
  82350. consecutive
  82351. consecutive
  82352. carbon
  82353. carbon
  82354. formation
  82355. allyl
  82356. consecutive
  82357. carbon
  82358. carbon
  82359. formation
  82360. allylpall
  82361. consecutive
  82362. rearrangements
  82363. consequence
  82364. consequences
  82365. quences
  82366. strain
  82367. hydrocarbons
  82368. consequenes
  82369. conservation
  82370. consideration
  82371. considerations
  82372. considerations
  82373. chiral
  82374. recognition
  82375. relevant
  82376. liquid
  82377. considerations
  82378. chiral
  82379. recognition
  82380. relevant
  82381. liquid
  82382. considerations
  82383. chiral
  82384. recognition
  82385. relevant
  82386. liquid
  82387. consiglio
  82388. constable
  82389. constable
  82390. metallosupramolecula
  82391. chemistry
  82392. constable
  82393. edwin
  82394. helices
  82395. supramolecular
  82396. chemistry
  82397. metal
  82398. constance
  82399. constanolactones
  82400. constant
  82401. constantinea
  82402. constantinos
  82403. constants
  82404. constituents
  82405. constitution
  82406. constitutional
  82407. constnnts
  82408. constrained
  82409. constraint
  82410. constraints
  82411. tructi
  82412. constructing
  82413. constructing
  82414. molecular
  82415. construction
  82416. considerations
  82417. chiral
  82418. recognition
  82419. relevant
  82420. liquid
  82421. constructi@
  82422. containing
  82423. containingnucleophil
  82424. contributions
  82425. controlled
  82426. convenient
  82427. efficient
  82428. conversion
  82429. aldehydes
  82430. acylated@
  82431. conversion
  82432. cooks
  82433. pradeep
  82434. wysocki
  82435. reactions
  82436. coordination
  82437. copper
  82438. catalysed
  82439. acyliminium
  82440. cyclisation
  82441. azabicyc@
  82442. cordell
  82443. angerhofer
  82444. pezzuto
  82445. recent
  82446. studies
  82447. cornils
  82448. hydroformylation
  82449. syntheses
  82450. carbon
  82451. monoxid@
  82452. costas@
  82453. coupling
  82454. couplings
  82455. 16-electron
  82456. piano-stool
  82457. molecules
  82458. molybdenum
  82459. crammer
  82460. properties
  82461. syntheses
  82462. sweetening
  82463. agen@
  82464. criddle
  82465. cross
  82466. crown
  82467. crystalline@
  82468. current
  82469. cyano
  82470. cyanothioacetamide@
  82471. cyclic
  82472. cyclisation
  82473. conformation
  82474. hydrocarbon
  82475. chains@
  82476. cyclization
  82477. construction
  82478. rolactones
  82479. acyclic
  82480. construction
  82481. carbon
  82482. frameworks
  82483. ruthenium
  82484. construction
  82485. fused
  82486. bicyclo
  82487. 5.3.0
  82488. decane
  82489. bicyclo
  82490. 5.4.0
  82491. construction
  82492. highly
  82493. efficient
  82494. salen
  82495. catalyst
  82496. asymm
  82497. construction
  82498. hydroxylated
  82499. alkaloids
  82500. mannonolactam
  82501. deoxyma
  82502. construction
  82503. synthetic
  82504. macrocyclic
  82505. compounds
  82506. possessing
  82507. construction
  82508. stemodane
  82509. nucleus
  82510. hydroxyl-directed
  82511. constructions
  82512. consuelo
  82513. consultants
  82514. contact
  82515. containingc
  82516. containing
  82517. containingnucleophil
  82518. containingnucleophil
  82519. contaminants
  82520. contaming
  82521. contemporary
  82522. contemporary
  82523. heterocyclic
  82524. chemistry
  82525. contemporary
  82526. ideas
  82527. about
  82528. conformations
  82529. eight-membered
  82530. contemporary
  82531. problems
  82532. methanol
  82533. synthesis
  82534. content
  82535. context
  82536. contiguous
  82537. continuation
  82538. continuous
  82539. continuum
  82540. contra
  82541. contra-electronic
  82542. contraction
  82543. contractions
  82544. contrapolarization
  82545. contrapolarization
  82546. concept
  82547. organic
  82548. reactivity
  82549. contrasteric
  82550. contrasteric
  82551. regiochemical
  82552. incorporation
  82553. stannylacetylene
  82554. contrasting
  82555. contreras
  82556. contreras
  82557. tamayo
  82558. transformations
  82559. diazaquinone
  82560. contribute
  82561. contribution
  82562. contributions
  82563. contributions
  82564. contributions
  82565. chemistry
  82566. lactam
  82567. antibiotics
  82568. 1-oxa
  82569. contributions
  82570. chemistry
  82571. phosphorus
  82572. monocyclic
  82573. control
  82574. acyclic
  82575. stereochemistry
  82576. control
  82577. asymmetry
  82578. through
  82579. conjugate
  82580. addition
  82581. reactions
  82582. control
  82583. regioselectivity
  82584. chelating
  82585. substrates
  82586. control
  82587. regioselectivity
  82588. nitrile
  82589. oxide
  82590. cycloadditions
  82591. control
  82592. selectivity
  82593. diels
  82594. alder
  82595. reactions
  82596. controlled
  82597. controlled
  82598. controlled
  82599. carbometallation
  82600. carbon-carbon
  82601. controlled
  82602. organic
  82603. synthesis
  82604. microporous
  82605. controller
  82606. controlling
  82607. controlling
  82608. radical
  82609. chain
  82610. reactions
  82611. unimolecular
  82612. chain
  82613. controlling
  82614. stereochemistry
  82615. radical
  82616. addition
  82617. cyclizat
  82618. controls
  82619. controversial
  82620. controversy
  82621. conus
  82622. convegent
  82623. convegent
  82624. synthesis
  82625. polyene
  82626. macrolide
  82627. roxaticin
  82628. convenient
  82629. convenient
  82630. efficient
  82631. conversion
  82632. aldehydes
  82633. acylated
  82634. convenient
  82635. general
  82636. synthesis
  82637. alkoxy
  82638. arylcycloprop
  82639. convenient
  82640. annulation
  82641. process
  82642. involving
  82643. tandem
  82644. alkylation
  82645. convenient
  82646. construction
  82647. cyclopentanones
  82648. cyclopentannu
  82649. convenient
  82650. preparation
  82651. trimethylsilyloxy
  82652. hydroxys
  82653. convenient
  82654. preparation
  82655. amino
  82656. propanol
  82657. convenient
  82658. preparations
  82659. diethyl
  82660. acylamino
  82661. methyl
  82662. phosphon
  82663. convenient
  82664. procedure
  82665. preparing
  82666. iodopropyl
  82667. methyl
  82668. convenient
  82669. procedure
  82670. selective
  82671. generation
  82672. allylzircon
  82673. convenient
  82674. unimolecular
  82675. sources
  82676. aryloxyl
  82677. radicals
  82678. photo
  82679. convergent
  82680. phase
  82681. peptide
  82682. synthesis
  82683. convergent
  82684. synthesis
  82685. aminobicyclo
  82686. 3.3.0
  82687. octenes
  82688. using
  82689. convergent
  82690. synthesis
  82691. polyether
  82692. ionophore
  82693. antibiotics
  82694. conversion
  82695. conversion
  82696. conversion
  82697. alkanes
  82698. silyl
  82699. ethers
  82700. silanes
  82701. conversion
  82702. amides
  82703. lactams
  82704. thioamides
  82705. thiolacta
  82706. conversion
  82707. lactams
  82708. versatile
  82709. synthons
  82710. molecul
  82711. conversion
  82712. dimethylhydrazones
  82713. carbonyl
  82714. compounds
  82715. conversion
  82716. lactams
  82717. versatile
  82718. synthons
  82719. molecular
  82720. conversion
  82721. primary
  82722. amine
  82723. other
  82724. functional
  82725. groups
  82726. conversion
  82727. saturated
  82728. ketones
  82729. 2-lithiodienes
  82730. conversions
  82731. conversions
  82732. primary
  82733. amino
  82734. groups
  82735. other
  82736. functionality
  82737. cooke
  82738. cooke
  82739. edwards
  82740. naturally
  82741. occurring
  82742. phenalenones
  82743. cooks
  82744. cooks
  82745. pradeep
  82746. wysocki
  82747. reactions
  82748. cookson
  82749. coolbaugh
  82750. cooled
  82751. cooley
  82752. cooper
  82753. cooper
  82754. david
  82755. michael
  82756. williams
  82757. organic
  82758. reactiv
  82759. cooper
  82760. stephen
  82761. crown
  82762. compounds
  82763. toward
  82764. future
  82765. applicatio
  82766. cooperation
  82767. cooperative
  82768. cooperative
  82769. effect
  82770. complexes
  82771. catalytic
  82772. activity
  82773. cooperativity
  82774. cooperativity
  82775. chirality
  82776. homog
  82777. neous
  82778. catalysis
  82779. coordinate
  82780. coordinated
  82781. coordinately
  82782. coordinates
  82783. inating
  82784. coordination
  82785. coordination
  82786. coordination
  82787. chemistry
  82788. dihydrogen
  82789. coordinatively
  82790. coote
  82791. oxy-cope
  82792. anionic
  82793. oxy-cope
  82794. rearrangements
  82795. coping
  82796. coping
  82797. extreme
  82798. lewis
  82799. acidity
  82800. strategies
  82801. synthes
  82802. copolymerization
  82803. copolymers
  82804. copperC
  82805. copper
  82806. assisted
  82807. nucleophilic
  82808. substitution
  82809. halogen
  82810. copper
  82811. assisted
  82812. substitution
  82813. reaction
  82814. phenylthio
  82815. group
  82816. copper
  82817. catalysed
  82818. acyliminium
  82819. cyclisation
  82820. azabicyc
  82821. copper
  82822. catalyzed
  82823. aziridination
  82824. olefins
  82825. toluenesulfon
  82826. copper
  82827. catalyzed
  82828. formation
  82829. reaction
  82830. allylzircona
  82831. copper
  82832. catalyzed
  82833. conjugate
  82834. addition
  82835. trimethylaluminium
  82836. copper
  82837. bromide
  82838. dimethyl
  82839. sulfide
  82840. complex
  82841. alternative
  82842. copper
  82843. catalysed
  82844. reactions
  82845. organolithiums
  82846. grignard
  82847. copper
  82848. catalyzed
  82849. amination
  82850. propargyl
  82851. esters
  82852. selective
  82853. copper
  82854. catalysis
  82855. complete
  82856. partial
  82857. oxidation
  82858. copper
  82859. rhodium
  82860. catalyzed
  82861. decomposition
  82862. diazo
  82863. compounds
  82864. copper-catalyzed
  82865. coppola
  82866. coppola
  82867. chemistry
  82868. isatoic
  82869. anhydride
  82870. corbridge
  82871. corbridge
  82872. phosphorus
  82873. elsevier
  82874. review
  82875. corcoran
  82876. corcoran
  82877. biosynthesis
  82878. antibiotics
  82879. springer
  82880. cordell
  82881. cordell
  82882. angerhofer
  82883. pezzuto
  82884. recent
  82885. studies
  82886. cordell
  82887. introduction
  82888. alkaloids
  82889. biogenetic
  82890. approach
  82891. cordell
  82892. aspidosperma
  82893. alkaloids
  82894. alkaloids
  82895. cordell
  82896. geoffrey
  82897. kinghorn
  82898. douglas
  82899. dimensional
  82900. proton
  82901. cordero
  82902. corey
  82903. zuckermann
  82904. schultz
  82905. hybrid
  82906. enzymes
  82907. corey
  82908. elias
  82909. james
  82910. logic
  82911. chemical
  82912. synthesis
  82913. multistep
  82914. corey's
  82915. corin
  82916. cornelis
  82917. cornelis
  82918. andre
  82919. laszlo
  82920. pierre
  82921. molding
  82922. clays
  82923. efficient
  82924. cornelisse
  82925. cornelisse
  82926. lodder
  82927. havinga
  82928. pathways
  82929. intermediates
  82930. cornelisse
  82931. photocycloaddition
  82932. arenes
  82933. cornell
  82934. cornforth
  82935. cornforth
  82936. warcup
  82937. trouble
  82938. synthesis
  82939. australian
  82940. cornils
  82941. cornils
  82942. herrmann
  82943. rasch
  82944. pioneer
  82945. industrial
  82946. cornils
  82947. hydroformylation
  82948. syntheses
  82949. carbon
  82950. monoxid
  82951. coronamic
  82952. corporation
  82953. corrado
  82954. correlation
  82955. correlation
  82956. braun
  82957. ritter
  82958. bischler-napieralski
  82959. correlations
  82960. corresponding
  82961. corrin
  82962. corrins
  82963. corriu
  82964. corroles
  82965. corset
  82966. corset
  82967. vibrational
  82968. infrared
  82969. raman
  82970. spectroscopy
  82971. corsi
  82972. corticoids
  82973. corticosteroid
  82974. corwin
  82975. corynantheioid
  82976. cosgrove
  82977. cosmic
  82978. cosse
  82979. cossinger
  82980. cossu
  82981. cossu
  82982. sergio
  82983. lucchi
  82984. ottorino
  82985. fabbri
  82986. davide
  82987. licini
  82988. giulia
  82989. cossy
  82990. cossy
  82991. janine
  82992. regio
  82993. stereoselective
  82994. cyclizations
  82995. applicat
  82996. costa
  82997. costamagna
  82998. costamagna
  82999. canales
  83000. vargas
  83001. camalli
  83002. mercedes
  83003. costantino
  83004. costas
  83005. costero
  83006. costero
  83007. chemistry
  83008. unsaturated
  83009. nitrogen
  83010. heterocy
  83011. cottard
  83012. cotton
  83013. cotton
  83014. hanson
  83015. fluxional
  83016. molecules
  83017. reversible
  83018. thermal
  83019. coucouvanis
  83020. coumarin
  83021. coumarin-crown
  83022. coumarins
  83023. coumestans
  83024. coumpounds
  83025. counsell
  83026. counterat
  83027. counterat
  83028. reagents
  83029. organic
  83030. reactions
  83031. counterattack
  83032. counterattack
  83033. reagents
  83034. organic
  83035. synthesis
  83036. counterattack
  83037. reagents
  83038. organic
  83039. synthesis
  83040. review
  83041. reagent
  83042. counterion
  83043. couple
  83044. coupled
  83045. coupled
  83046. organolanthanide-cat
  83047. c-n/c-c
  83048. formation
  83049. processe
  83050. coupling
  83051. coupling
  83052. reactions
  83053. between
  83054. carbon
  83055. centers
  83056. coupling
  83057. reactions
  83058. between
  83059. carbon
  83060. centers
  83061. coupling
  83062. reactions
  83063. between
  83064. carbon
  83065. centers
  83066. coupling
  83067. reactions
  83068. between
  83069. carbon
  83070. centers
  83071. coupling
  83072. reagents
  83073. peptide
  83074. synthesis
  83075. couplings
  83076. couplings
  83077. course
  83078. courtneidge
  83079. courtney
  83080. courtois
  83081. courtot
  83082. cousins
  83083. cousins
  83084. saturated
  83085. unsaturated
  83086. hydrocarbons
  83087. contemp
  83088. cousse
  83089. covalent
  83090. covalent
  83091. versus
  83092. dative
  83093. bonds
  83094. group
  83095. metals
  83096. useful
  83097. covalently
  83098. cover
  83099. coverage
  83100. covered
  83101. covering
  83102. coville
  83103. cowan
  83104. simpkins
  83105. nigel
  83106. asymmetric
  83107. synthesis
  83108. using
  83109. homoc
  83110. coxon
  83111. coxon
  83112. james
  83113. mcdonald
  83114. quentin
  83115. steel
  83116. peter
  83117. diastereofaci
  83118. coyle
  83119. coyle
  83120. photochemistry
  83121. carboxylic
  83122. derivatives
  83123. 16-electron
  83124. piano-stool
  83125. molecules
  83126. molybdenum
  83127. cp-70429
  83128. cp2rh2
  83129. cp2tich2
  83130. cp2tich2
  83131. complexes
  83132. synthetic
  83133. applications
  83134. cpmas
  83135. cra's
  83136. crabbj
  83137. crabb
  83138. patel
  83139. alicyclic
  83140. hydrocarbons
  83141. conformation
  83142. crabtree
  83143. crafting
  83144. crafts
  83145. cragg
  83146. cragg
  83147. organoborates
  83148. organic
  83149. synthesis
  83150. craig
  83151. craik
  83152. craine
  83153. design
  83154. complexes
  83155. between
  83156. synthetic
  83157. trueblood
  83158. concept
  83159. structure
  83160. binding
  83161. donald
  83162. discovery
  83163. design
  83164. organic
  83165. chemistry
  83166. cram'sI
  83167. cramer
  83168. cramer
  83169. christopher
  83170. famini
  83171. george
  83172. lowrey
  83173. alfred
  83174. crammer
  83175. crammer
  83176. properties
  83177. syntheses
  83178. sweetening
  83179. crandall
  83180. crane
  83181. crass
  83182. crats
  83183. craven
  83184. crawford
  83185. crawford
  83186. crawford
  83187. synthesis
  83188. ascorbic
  83189. crawford
  83190. gulono
  83191. lactones
  83192. review
  83193. their
  83194. synthe
  83195. crayston
  83196. crayston
  83197. iraqi
  83198. walton
  83199. polyradicals
  83200. synthesis
  83201. spect
  83202. handbook
  83203. chromatography
  83204. carbohydrates
  83205. handbook
  83206. organic
  83207. photochemistry
  83208. crcl2
  83209. mediated
  83210. allylation
  83211. protected
  83212. amino
  83213. aldehydes
  83214. creary
  83215. creary
  83216. xavier
  83217. electronegatively
  83218. substituted
  83219. carbocations
  83220. creary
  83221. xavier
  83222. reactions
  83223. halodiazirines
  83224. electro
  83225. creation
  83226. creativity
  83227. creed
  83228. creene
  83229. creitical
  83230. cremer
  83231. crews
  83232. cribbs
  83233. crich
  83234. criddle
  83235. criddle
  83236. criller
  83237. crimmins
  83238. crimmins
  83239. nantermet
  83240. homoenolates
  83241. other
  83242. functional
  83243. crinane
  83244. ristol
  83245. criteria
  83246. criteriain
  83247. criterion
  83248. critical
  83249. criticisms
  83250. croat
  83251. crobial
  83252. crockett
  83253. crockett
  83254. nigel
  83255. alefounder
  83256. peter
  83257. battersby
  83258. abell
  83259. croconate
  83260. croft
  83261. crombie
  83262. crombie
  83263. natural
  83264. products
  83265. sesquicentenary
  83266. cromwell
  83267. cromwell
  83268. phillips
  83269. azetidines
  83270. recent
  83271. synthetic
  83272. develo
  83273. crosby
  83274. crosby
  83275. synthesis
  83276. optically
  83277. active
  83278. compounds
  83279. large
  83280. crossC
  83281. cross
  83282. cross
  83283. coupling
  83284. between
  83285. functionalized
  83286. alkylcopper
  83287. reagents
  83288. cross-conjugated
  83289. cross-conjugated
  83290. systems
  83291. cycloheptatrienes
  83292. tropenes
  83293. tropo
  83294. cross-conjugated
  83295. systems
  83296. cyclononatetraenes
  83297. cross-conjugated
  83298. systems
  83299. cyclopentadiones
  83300. 6-heteropentafu
  83301. cross-conjugated
  83302. systems
  83303. cyclopro
  83304. cyclopropenones
  83305. cross-coulping
  83306. cross-coupling
  83307. cross-coupling
  83308. reactions
  83309. based
  83310. acetals
  83311. crossed
  83312. crossing
  83313. crossover
  83314. crossroads
  83315. crotyl
  83316. cetaldehyd
  83317. crotylsilanes
  83318. crotylsilylation
  83319. crounse
  83320. crowded
  83321. crowe
  83322. crowley
  83323. crown
  83324. crown
  83325. crown
  83326. compounds
  83327. toward
  83328. future
  83329. applications
  83330. crown
  83331. ethers
  83332. analogous
  83333. compounds
  83334. crown
  83335. ethers
  83336. analogs
  83337. crown
  83338. ethers
  83339. cryptands
  83340. crown
  83341. ethers
  83342. macrocyclic
  83343. complexing
  83344. agents
  83345. crown-ethers
  83346. crozier
  83347. crucial
  83348. crude
  83349. cryoimmobilized
  83350. cryoimmobilized
  83351. enzymes
  83352. cells
  83353. organic
  83354. synthesis
  83355. cryptand
  83356. cryptands
  83357. cryptates
  83358. cryptaustoline
  83359. cryptaustoline
  83360. synthesis
  83361. revision
  83362. absolute
  83363. stereochemistr
  83364. cryptophanes
  83365. cryptophanes
  83366. eceptors
  83367. tetrahedral
  83368. molecules
  83369. cryptopleurine
  83370. crystalline
  83371. crystallization
  83372. crystallographic
  83373. crystallography
  83374. crystals
  83375. csaba
  83376. csicsery
  83377. csicsery
  83378. metal
  83379. catalyzed
  83380. dehydrocyclization
  83381. alkylarom
  83382. csizmadia
  83383. csizmadia
  83384. theoretical
  83385. studies
  83386. positively
  83387. charged
  83388. csp3-s
  83389. cterial
  83390. ctronic
  83391. ctures
  83392. cubane
  83393. cubanes
  83394. cubanes
  83395. starting
  83396. materials
  83397. chemist
  83398. 1990s
  83399. cubitanoids
  83400. cucl2
  83401. cuether
  83402. cuevas
  83403. cuiix2
  83404. cular
  83405. cularine
  83406. culprits
  83407. cultivated
  83408. culture
  83409. cultures
  83410. cumambulatory
  83411. cumulated
  83412. cumulated
  83413. ylides
  83414. reactions
  83415. triphenylphosphorany
  83416. etheno
  83417. cumulene
  83418. cumulenes
  83419. cundall
  83420. cunico
  83421. cuparane
  83422. cuppedophanes
  83423. cuprate
  83424. cupration
  83425. cupric
  83426. curacin
  83427. curci
  83428. curiosity
  83429. curran
  83430. curran
  83431. dennis
  83432. fevig
  83433. thomas
  83434. jasperse
  83435. craig
  83436. totleben
  83437. curran
  83438. dennis
  83439. radical
  83440. reactions
  83441. retrosynthetic
  83442. plannin
  83443. current
  83444. current
  83445. current
  83446. approach
  83447. problem
  83448. nitrenium
  83449. current
  83450. state
  83451. organocobalt
  83452. organorhodium
  83453. chemis
  83454. curriu
  83455. curtin
  83456. curtin
  83457. chemical
  83458. consequences
  83459. polar
  83460. curtin-hammett
  83461. curtis
  83462. curtis
  83463. epstein
  83464. redistribution
  83465. reactions
  83466. silicon
  83467. curtius
  83468. cusack
  83469. cusmano
  83470. cutler
  83471. cx-co
  83472. lophanes
  83473. cyamide
  83474. cyanates
  83475. cyanation
  83476. cyanation
  83477. aromatic
  83478. halides
  83479. cyanic
  83480. cyanide
  83481. cyanides
  83482. cyanine
  83483. cyano
  83484. cyano
  83485. cyano-borates
  83486. cyanoacetamide
  83487. cyanoacetylenes
  83488. cyanoalkynes
  83489. cyanoalkynes
  83490. magic
  83491. wands
  83492. preparation
  83493. novel
  83494. aromat
  83495. cyanoamines
  83496. cyanobacterium
  83497. cyanoborohydride
  83498. cyanocarbons
  83499. cyanocup
  83500. cyanocuprate
  83501. cyanocuprate
  83502. mediated
  83503. intramolecular
  83504. biaryl
  83505. couplings
  83506. applie
  83507. cyanocuprate-catalyz
  83508. cyanocuprate-catalyz
  83509. 14-additions
  83510. vinylic
  83511. zirconocenes
  83512. cyanocuprates
  83513. cyanoethylation
  83514. cyanoethylation
  83515. herman
  83516. bruson
  83517. organic
  83518. reactions
  83519. volume
  83520. cyanogen
  83521. cyanohydrin
  83522. cyanohydrins
  83523. cyanoketene
  83524. cyanoketenes
  83525. cyanoketenes
  83526. synthesis
  83527. cycloadditions
  83528. cyanoketones
  83529. cyanomethylene
  83530. cyanomethylene
  83531. phosphoranes
  83532. novel
  83533. carbonyl
  83534. dipole
  83535. cyanooxiranes
  83536. cyanoprop
  83537. cyanopropylthio
  83538. cyanothioacetamide
  83539. cyanothioacrylamides
  83540. cyanotrimethylsilane
  83541. cyanotrimethylsilane
  83542. versatile
  83543. reagent
  83544. introducing
  83545. cyathins
  83546. cybulski
  83547. cyclacene
  83548. cyclazines
  83549. cycle
  83550. cyclenones
  83551. cycles
  83552. cycli
  83553. cyclialkyation
  83554. cyclialkylation
  83555. cyclialkylations
  83556. cyclialkylations
  83557. conjugated
  83558. dienones
  83559. furans
  83560. cyclic^
  83561. cyclic
  83562. aldoses
  83563. aldosides
  83564. cyclic
  83565. alkynes
  83566. dienynes
  83567. synthetic
  83568. challenge
  83569. cyclic
  83570. hydroxylamines
  83571. review
  83572. preparative
  83573. methods
  83574. cyclic
  83575. isomeric
  83576. membered
  83577. membered
  83578. hetero
  83579. dinuclear
  83580. cyclic
  83581. diphosphazenes
  83582. cyclic
  83583. sulfides
  83584. organic
  83585. synthesis
  83586. cyclic
  83587. sulfites
  83588. cyclic
  83589. sulfates
  83590. epoxide
  83591. synthons
  83592. cyclic
  83593. sulfites
  83594. cyclic
  83595. sulfates
  83596. epoxide
  83597. ynthons
  83598. cyclisation
  83599. cyclisation
  83600. conformation
  83601. hydrocarbon
  83602. chains
  83603. cyclisation
  83604. alkoxy
  83605. radicals
  83606. semiempirical
  83607. cyclisation
  83608. dialdehydes
  83609. nitromethane
  83610. cyclisation
  83611. ylidenemalononitrile
  83612. cyclisations
  83613. cyclisations
  83614. electrochemical
  83615. activation
  83616. cyclitol
  83617. cyclitols
  83618. cyclitols
  83619. their
  83620. derivatives
  83621. handhook
  83622. physical
  83623. spect
  83624. cyclization
  83625. cyclization
  83626. cyclization
  83627. coupling
  83628. rearrangement
  83629. reactions
  83630. organozi
  83631. cyclization
  83632. a-amino
  83633. anions
  83634. cyclization
  83635. carbinyl
  83636. radicals
  83637. imines
  83638. hydrazones
  83639. cyclization
  83640. acetyl
  83641. ortho
  83642. chlorophenyl
  83643. aminobut
  83644. cyclization
  83645. reactions
  83646. cyclization
  83647. reactions
  83648. allylic
  83649. o-stannyl
  83650. ketyls
  83651. cyclization-cycloadd
  83652. cyclizations
  83653. cyclizations
  83654. catalyzed
  83655. allylic
  83656. alkylations
  83657. cyclizations
  83658. palladium-catalyzed
  83659. allylic
  83660. alkylation
  83661. cyclizations
  83662. diazoketones
  83663. cyclizaton
  83664. cyclize
  83665. cyclized
  83666. cycloc
  83667. cycloa
  83668. cycloadd
  83669. cycloadd
  83670. cyclocondensation
  83671. reactions
  83672. highly
  83673. cycloadditio
  83674. cycloaddition
  83675. cyclizations
  83676. cyclizations
  83677. palladium
  83678. catalyzed
  83679. allylic
  83680. alkylations@
  83681. unsaturated
  83682. sulfo@
  83683. cycloaddition
  83684. reactions
  83685. heteroaromatic
  83686. membered
  83687. rings@
  83688. cycloadditions
  83689. allenes
  83690. reactions
  83691. unusual
  83692. mechanistic
  83693. cycloalkenylidene@
  83694. cyclobutarenes
  83695. chemistry
  83696. benzocyclobutene
  83697. biphenylene@
  83698. cyclodextrins
  83699. off-the-shelf
  83700. components
  83701. construction
  83702. cyclohexyl@
  83703. cyclopalladated
  83704. cyclopentanes
  83705. cyclophanes
  83706. cyclopropanecarboxyl
  83707. cyclopropenes@
  83708. cyclopropylthiocarbe@
  83709. cyvin
  83710. cyvin
  83711. bjorg
  83712. brunvoll
  83713. enumeration
  83714. benze@
  83715. barton
  83716. synthesis
  83717. specifically
  83718. fluorinated
  83719. natural
  83720. raduz
  83721. syntheses
  83722. activity
  83723. heteroprostan@
  83724. preparation
  83725. nucleoside
  83726. phosphorothioates
  83727. phosph@
  83728. danelon
  83729. gerardo
  83730. mascaretti
  83731. oreste
  83732. fluorinated
  83733. penicillin@
  83734. darszon
  83735. david
  83736. cycloaddition
  83737. cycloaddition
  83738. cyclization
  83739. reactions
  83740. unsaturated
  83741. sulfo
  83742. cycloaddition
  83743. cyclocondensation
  83744. reactions
  83745. highly
  83746. cycloaddition
  83747. approach
  83748. synthesis
  83749. hindered
  83750. cycloaddition
  83751. synthesis
  83752. sulfonamide
  83753. derivatives
  83754. cycloaddition
  83755. allyl
  83756. cations
  83757. dienes
  83758. method
  83759. cycloaddition
  83760. nitrile
  83761. oxides
  83762. oxobut
  83763. enoic
  83764. cycloaddition
  83765. nitrile
  83766. oxides
  83767. homochiral
  83768. vinyl
  83769. ethers
  83770. cycloaddition
  83771. nitrile
  83772. oxides
  83773. multiple
  83774. bonds
  83775. containing
  83776. cycloaddition
  83777. reaction
  83778. allenes
  83779. review
  83780. cycloaddition
  83781. reactions
  83782. carbohydrate
  83783. chemistry
  83784. cycloaddition
  83785. reactions
  83786. carbohydrate
  83787. chemistry
  83788. overvie
  83789. cycloaddition
  83790. reactions
  83791. organic
  83792. synthesis
  83793. cycloaddition
  83794. reactions
  83795. benzo
  83796. thiete
  83797. compounds
  83798. cycloaddition
  83799. reactions
  83800. aliphatic
  83801. aromatic
  83802. isocy
  83803. cycloaddition
  83804. reactions
  83805. hetero
  83806. azadienes
  83807. intramolecular
  83808. cycloaddition
  83809. reactions
  83810. heteroaromatic
  83811. membered
  83812. rings
  83813. cycloaddition
  83814. reactions
  83815. heteroaromatic
  83816. six-membered
  83817. rings
  83818. cycloaddition
  83819. opening
  83820. other
  83821. reactions
  83822. thiophenes
  83823. cycloadditions
  83824. cycloadditions
  83825. stereoselective
  83826. formation
  83827. functionalize
  83828. cycloadditions
  83829. allenes
  83830. reactions
  83831. unusual
  83832. mechanistic
  83833. cycloadditions
  83834. fluoroallene
  83835. 11-difluoroallene
  83836. cycloadditions
  83837. ketenes
  83838. keteniminium
  83839. salts
  83840. alkene
  83841. cycloadditions
  83842. organometal
  83843. fragment
  83844. substituted
  83845. alkenes
  83846. cycloadditions
  83847. six-membered
  83848. heteroaromatic
  83849. betaines
  83850. cycloadditions-defin
  83851. cycloadditions-defin
  83852. classification
  83853. characterisation
  83854. cycloadditive
  83855. cycloadditon
  83856. cycloadduct
  83857. cycloadducts
  83858. cycloalkadiynes
  83859. cycloalkadiynes-from
  83860. cycloalkadiynes-from
  83861. triple
  83862. bonds
  83863. strain
  83864. cycloalkane
  83865. cycloalkanes
  83866. cycloalkanols
  83867. cycloalkanone
  83868. cycloalkenes
  83869. cycloalkenes
  83870. intramolecular
  83871. wittig
  83872. reaction
  83873. cycloalkenones
  83874. cycloalkenopyridines
  83875. cycloalkenyl
  83876. cycloalkenylidene
  83877. cycloalkenylidenes
  83878. cycloalkenynes
  83879. cycloalkyl
  83880. cycloalkylation
  83881. cycloalkylidenes
  83882. cycloalkynes
  83883. cycloaromatization
  83884. cycloartenol
  83885. cyclobisalkylation
  83886. cycloboranes
  83887. cyclobutadiene
  83888. cyclobutadienemetal
  83889. cyclobutadienemetal
  83890. complexes
  83891. cyclobutadienoids
  83892. cyclobutane
  83893. cyclobutane
  83894. derivatives
  83895. thermal
  83896. cycloaddition
  83897. reactions
  83898. cyclobutane
  83899. contractions
  83900. involving
  83901. carbonium
  83902. cyclobutanesh
  83903. cyclobutanes
  83904. photochemical
  83905. metal-catalysed
  83906. cation-r
  83907. cyclobutanols
  83908. cyclobutanone
  83909. cyclobutanones
  83910. cyclobutarenes
  83911. cyclobutarenes
  83912. biphenyleno
  83913. biphenylene
  83914. cyclobutarenes
  83915. chemistry
  83916. benzocyclobutene
  83917. biphenylene
  83918. cyclobutendione
  83919. cyclobutene
  83920. cyclobutene
  83921. opening
  83922. reactions
  83923. cyclobutene-12-dione
  83924. cyclobutenedione
  83925. cyclobutenones-synth
  83926. cyclobutenyl
  83927. cyclobutyl
  83928. cyclobutylamines
  83929. cyclobutylcarbinyl
  83930. cyclobutylidene
  83931. cyclocarbonylation
  83932. cyclocarbonylation
  83933. enynes
  83934. promoted
  83935. carbonyls
  83936. cyclocondensation
  83937. cyclocopolymerizatio
  83938. cyclodextrin
  83939. cyclodextrin
  83940. complexation
  83941. amphiphilic
  83942. compounds
  83943. cyclodextrins
  83944. cyclodextrins
  83945. their
  83946. applications
  83947. analytical
  83948. chemistry
  83949. cyclodextrins
  83950. building
  83951. blocks
  83952. supramolecular
  83953. structur
  83954. cyclodextrins
  83955. second-sphere
  83956. ligands
  83957. transition
  83958. metal
  83959. cyclodextrins
  83960. off-the-shelf
  83961. components
  83962. construction
  83963. cyclodimerization
  83964. cyclododecatriene
  83965. cycloelimination
  83966. cyclofunctionalizati
  83967. cyclohepta
  83968. cyclohepta
  83969. benzoxazine
  83970. related
  83971. compounds
  83972. cycloheptadien
  83973. cycloheptadiene
  83974. cycloheptanesa
  83975. cycloheptanones
  83976. cycloheptatrienes
  83977. cycloheptatrienylium
  83978. cycloheptatrienylium
  83979. tropylium
  83980. salts
  83981. cycloheptene
  83982. cyclohex
  83983. cyclohexa
  83984. cyclohexa-35-diene-1
  83985. cyclohexadien
  83986. cyclohexadienec
  83987. cyclohexadienesb
  83988. cyclohexadienones
  83989. cyclohexanec
  83990. cyclohexanecarboxyli
  83991. cyclohexanes
  83992. cyclohexanols
  83993. cyclohexanone
  83994. cyclohexene
  83995. cyclohexenes
  83996. cyclohexenols
  83997. cyclohexenone
  83998. cyclohexenones
  83999. cyclohexyl
  84000. cyclohexyl
  84001. based
  84002. chiral
  84003. auxiliaries
  84004. cyclohexyl-based
  84005. cyclohexyl-based
  84006. chiral
  84007. auxiliaries
  84008. cyclohexylideneacety
  84009. cyclohexylideneacety
  84010. isothiocyanate
  84011. precursor
  84012. synthe
  84013. cyclohomologues
  84014. cyclohydrocarbonylat
  84015. cycloisomerization
  84016. cycloisomerizations
  84017. cyclomagnesiation
  84018. cyclomalto
  84019. cyclomalto-oligosacc
  84020. cyclomers
  84021. cyclometalation
  84022. cyclometalation
  84023. reactions
  84024. cyclononatetraenes
  84025. cyclononatetraenyl
  84026. cyclononatetraenyl
  84027. anions
  84028. cycloocta
  84029. cyclooctadiene
  84030. cyclooctane
  84031. cyclooctanesa
  84032. cyclooctanoids
  84033. cyclooctanols
  84034. cyclooctatetraene
  84035. cyclooctatetraene
  84036. dianions
  84037. cyclooctatetraenes
  84038. cyclooctatetraenes
  84039. conformational
  84040. pi-electronic
  84041. dynamics
  84042. cyclooctatriene
  84043. cycloolefinic
  84044. cycloologomerization
  84045. cyclopalladated
  84046. cyclopalladated
  84047. cyclopalladated
  84048. complexes
  84049. organic
  84050. synthesis
  84051. cyclopalladized
  84052. cyclopendant
  84053. cyclopenenoid
  84054. cyclopent
  84055. cyclopent
  84056. indene
  84057. benzopentalene
  84058. generation
  84059. flash
  84060. vacuum
  84061. cyclopent-2-enone
  84062. cyclopenta
  84063. cyclopenta
  84064. annellation
  84065. reactions
  84066. organic
  84067. synthesis
  84068. cyclopentadienee
  84069. cyclopentadienes
  84070. cyclopentadienides
  84071. cyclopentadienyl
  84072. cyclopentadienyl
  84073. anions
  84074. cyclopentadienyl
  84075. complexes
  84076. actinides
  84077. formation
  84078. cyclopentadienyl
  84079. molybdenum
  84080. tungsten
  84081. dihalides
  84082. cyclopentadienyl-rin
  84083. cyclopentadienyl-tra
  84084. cyclopentadienylides
  84085. cyclopentadienylme
  84086. cyclopentadienylmeth
  84087. cyclopentadiones
  84088. cyclopentanef
  84089. cyclopentanediones
  84090. cyclopentanesg
  84091. cyclopentanes
  84092. cyclopentannelation
  84093. cyclopentannelation
  84094. reactions
  84095. organic
  84096. synthesis
  84097. cyclopentannelltion
  84098. cyclopentannulation
  84099. cyclopentanoid
  84100. cyclopentanoid-fused
  84101. cyclopentanoids
  84102. cyclopentanoids
  84103. challenge
  84104. methodology
  84105. cyclopentanone
  84106. cyclopentanones
  84107. cyclopentaunnellatio
  84108. cyclopentaunnellatio
  84109. reactions
  84110. organic
  84111. synthesis
  84112. cyclopenten
  84113. cyclopentene
  84114. cyclopentenes
  84115. opentenoid
  84116. cyclopentenols
  84117. cyclopentenone
  84118. cyclopentenone
  84119. synthesis
  84120. allylidene
  84121. triphenylphosphoran
  84122. cyclopentenones
  84123. cyclopentenones
  84124. pyrrolidinones
  84125. intramolecular
  84126. carben
  84127. cyclopentenyl
  84128. cyclopentyl
  84129. cyclopentylamines
  84130. cyclopentylidene
  84131. cyclopeptides
  84132. cycloperoxyiodinatio
  84133. cyclophanes
  84134. cyclophanes
  84135. cyclophanes
  84136. synthetic
  84137. receptors
  84138. cyclophanes
  84139. vinylarenes
  84140. cyclophosphamide
  84141. cyclophosphazenes
  84142. cyclopolyenyl
  84143. cyclopolymerization
  84144. cyclopolysilanes
  84145. cyclopro
  84146. cyclopropanation
  84147. ation
  84148. silyl
  84149. ethers
  84150. cyclopropanation
  84151. unsaturated
  84152. ketosulphones
  84153. cyclopropanation/cop
  84154. cyclopropanations
  84155. cyclopropane
  84156. cyclopropane
  84157. derived
  84158. reactive
  84159. intermediates
  84160. cyclopropane-contain
  84161. cyclopropane-contain
  84162. eicosanoids
  84163. marine
  84164. orgin
  84165. biomimetic
  84166. cyclopropanecarboxyl
  84167. cyclopropanecarboxyl
  84168. cyclopropanedicarbox
  84169. cyclopropanediyldiph
  84170. cyclopropanesi
  84171. cyclopropanes
  84172. nucleophilic
  84173. attack
  84174. diaryl
  84175. cyclopropanes
  84176. reaction
  84177. transition-metal-car
  84178. complexe
  84179. cyclopropanes
  84180. unsaturated
  84181. compounds
  84182. methylene
  84183. iodide
  84184. cyclopropano
  84185. cyclopropano
  84186. amino
  84187. acids
  84188. 34-methamino
  84189. acids
  84190. cyclopropanol
  84191. cyclopropanol
  84192. chemistry
  84193. cyclopropanols
  84194. cyclopropanone
  84195. cyclopropanone
  84196. hemiacetals
  84197. cyclopropanones
  84198. cyclopropanylidene
  84199. cycloproparene
  84200. cycloproparenes
  84201. cyclopropene
  84202. cyclopropenecarboxyl
  84203. cyclopropenes
  84204. cyclopropenes
  84205. reagents
  84206. synthesis
  84207. cycloaddition
  84208. reacti
  84209. cyclopropenethiones
  84210. cyclopropenimines
  84211. cyclopropenone
  84212. cyclopropenones
  84213. cyclopropenyl
  84214. cyclopropenyl
  84215. radicals
  84216. anions
  84217. cyclopropenylium
  84218. cyclopropenylium
  84219. cations
  84220. cyclopropenylstannan
  84221. cyclopropenylzinc
  84222. cyclopropones
  84223. cyclopropyl
  84224. cyclopropylaminosulf
  84225. cyclopropylcarbene
  84226. cyclopropylcarbene
  84227. chromium
  84228. complexes
  84229. versatile
  84230. reagents
  84231. cyclopropylcarbene-c
  84232. cyclopropylcarbene-c
  84233. complexes
  84234. versatile
  84235. reagents
  84236. cyclopropylcarbinyl
  84237. cyclopropylidene
  84238. cyclopropyliminium
  84239. cyclopropylmethyl
  84240. cyclopropylsilanes
  84241. cyclopropylsulfides
  84242. cyclopropylthiocarbe
  84243. cycloproteins
  84244. cycloreversion
  84245. cycloreversions
  84246. cyclosiloxanes
  84247. cyclosporine
  84248. cyclotetrathioether
  84249. cyclotrimerization
  84250. cyclotriveratrylenes
  84251. cyclotriveratrylenes
  84252. cryptophanes
  84253. their
  84254. synthesis
  84255. cyclotron
  84256. cycoaddition
  84257. cylclisations
  84258. cylindracea
  84259. cylization
  84260. cyloaddition
  84261. cymantrene
  84262. cynthia
  84263. cyril
  84264. cystals
  84265. cystine
  84266. cytochalasan
  84267. cytochalasan
  84268. synthesis
  84269. macrocycle
  84270. formation
  84271. intramolecul
  84272. cytochalasans
  84273. cytochrome
  84274. cytotoxic
  84275. cytotoxicity
  84276. cyvinR
  84277. cyvin
  84278. brunvoll
  84279. cyvin
  84280. zhang
  84281. theory
  84282. cyvin
  84283. brunvoll
  84284. cyvin
  84285. theory
  84286. coronoid
  84287. hydrocarbo
  84288. cyvin
  84289. cyvin
  84290. bjorg
  84291. brunvoll
  84292. enumeration
  84293. benze
  84294. czarnik
  84295. czarnik
  84296. anthony
  84297. fluorescent
  84298. chemosensors
  84299. metal
  84300. czech
  84301. czechoslovakia
  84302. czernuszewicz
  84303. czeskis
  84304. czeskis
  84305. ivanova
  84306. moiseenkov
  84307. nefedov
  84308. chemi
  84309. czugler
  84310. arigoni
  84311. stereochemical
  84312. bremner
  84313. britain
  84314. chemical
  84315. ultrasonics
  84316. bryce
  84317. smith
  84318. gilbert
  84319. organic
  84320. photochemistry
  84321. benzen
  84322. billington
  84323. allylnickel
  84324. halide
  84325. palmer
  84326. strauss
  84327. benzomorphans
  84328. synthesis
  84329. stereoche
  84330. craig
  84331. stereochemical
  84332. aspects
  84333. kuhla
  84334. lombardino
  84335. pyrrolodiazines
  84336. bridgehe
  84337. fferences
  84338. photochemical
  84339. reactivity
  84340. 910-ethenoanthrac
  84341. whitten
  84342. quina
  84343. sprintschnik
  84344. sprint
  84345. acetic
  84346. anhydride
  84347. synthet
  84348. barton
  84349. inventi
  84350. barton
  84351. synthesis
  84352. specifically
  84353. fluorinated
  84354. natural
  84355. ivanov
  84356. vassilev
  84357. panayotov
  84358. synthesis
  84359. synthe
  84360. aberhart
  84361. biosynthesis
  84362. lactam
  84363. antibiotics
  84364. anderson
  84365. hassner
  84366. synthesis
  84367. synthesis
  84368. burton
  84369. hahnfeld
  84370. preparation
  84371. reactions
  84372. faulkner
  84373. marine
  84374. natural
  84375. products
  84376. chemistry
  84377. raber
  84378. guida
  84379. bu4nbh
  84380. boger
  84381. diels
  84382. alder
  84383. reactions
  84384. lednicer
  84385. mitscher
  84386. organic
  84387. chemistry
  84388. synthe
  84389. liotta
  84390. tetrahedron
  84391. recent
  84392. aspects
  84393. organose
  84394. doddrell
  84395. structural
  84396. applications
  84397. nuclear
  84398. lattice
  84399. sturmer
  84400. syntheses
  84401. properties
  84402. cyanine
  84403. related
  84404. moderhack
  84405. synthesis
  84406. membered
  84407. rings
  84408. murthy
  84409. synthesis
  84410. recent
  84411. advances
  84412. reinhoudt
  84413. cycloaddition
  84414. cycloreversion
  84415. react
  84416. raduz
  84417. syntheses
  84418. activity
  84419. heteroprostan
  84420. satchell
  84421. metal
  84422. promoted
  84423. reactions
  84424. organosulfur
  84425. paquer
  84426. france
  84427. reactions
  84428. organom
  84429. adams
  84430. bhatnagar
  84431. prins
  84432. reaction
  84433. matteson
  84434. organometal
  84435. directed
  84436. matteson
  84437. synthesis
  84438. methanetetraboronic
  84439. black
  84440. crozier
  84441. davis
  84442. synthesis
  84443. d'angelo
  84444. d'angelo
  84445. desmaele
  84446. didier
  84447. dumas
  84448. francoise
  84449. guingant
  84450. andre
  84451. d'auria
  84452. d'yachenko
  84453. d-alkenylimines
  84454. d-block
  84455. d-chiral
  84456. d-glucose
  84457. d-o-a
  84458. d-unsaturated
  84459. d1/d3
  84460. d2-isoxazoline
  84461. dabor
  84462. daboun
  84463. dactomelynes
  84464. dactylol
  84465. daemen
  84466. dagaut
  84467. dagmar
  84468. preparation
  84469. nucleoside
  84470. phosphorothioates
  84471. phosph
  84472. nature
  84473. stacking
  84474. interactions
  84475. between
  84476. organic
  84477. dahlhoff
  84478. dahne
  84479. daily
  84480. daimay
  84481. dakin
  84482. dakin-west
  84483. dal'nikovskaya
  84484. dalcanale
  84485. stereochemistry
  84486. conformational
  84487. analysis
  84488. verlag
  84489. conformation
  84490. complexes
  84491. oligoethers
  84492. johannes
  84493. contrasting
  84494. behavior
  84495. oxirane
  84496. oxetan
  84497. dallas
  84498. dalley
  84499. dalley
  84500. structural
  84501. studies
  84502. synthetic
  84503. macrocyclic
  84504. molec
  84505. daloutin
  84506. daloze
  84507. dalrymple
  84508. dalton
  84509. dalton
  84510. alkaloids
  84511. fundamental
  84512. chemistry
  84513. biogene
  84514. damage
  84515. damentals
  84516. damji
  84517. dammel
  84518. damrauer
  84519. damrauer
  84520. robert
  84521. phase
  84522. studies
  84523. negative
  84524. chemis
  84525. dance
  84526. dandia
  84527. daneel
  84528. danelon
  84529. danelon
  84530. gerardo
  84531. mascaretti
  84532. oreste
  84533. fluorinated
  84534. penicillin
  84535. danen
  84536. daneo
  84537. dangyan
  84538. danial
  84539. daniel
  84540. daniela
  84541. daniele
  84542. daniella
  84543. danil
  84544. danil
  84545. namor
  84546. angela
  84547. blackett
  84548. peter
  84549. garrido
  84550. pardo
  84551. maria
  84552. danil
  84553. namor
  84554. angela
  84555. marie
  84556. claude
  84557. lewis
  84558. david
  84559. danil
  84560. namor
  84561. angela
  84562. thermodynamics
  84563. supramolecular
  84564. danilov
  84565. danishefsky
  84566. danishefsky
  84567. electrophilic
  84568. cyclopropanes
  84569. organic
  84570. synthes
  84571. danishefsky
  84572. siloxy
  84573. dienes
  84574. total
  84575. synthesis
  84576. danishefsky's
  84577. dannecker
  84578. dannenberg
  84579. daphniphyllum
  84580. darbarwar
  84581. darensbourg
  84582. darfler
  84583. darfler
  84584. tometsko
  84585. applications
  84586. light
  84587. sensitive
  84588. daria
  84589. darias
  84590. dario
  84591. darren
  84592. darrick
  84593. darszon
  84594. darszon
  84595. darvill
  84596. darwish
  84597. darzens
  84598. darzens
  84599. glycidic
  84600. ester
  84601. condensation
  84602. database
  84603. databases
  84604. dative
  84605. dattoio
  84606. dauben
  84607. dauben
  84608. mcinnis
  84609. michno
  84610. photochemical
  84611. rearrangemen
  84612. dauksas
  84613. dauksas
  84614. purvaneckas
  84615. udenaite
  84616. gineityte
  84617. barau
  84618. czernuszewicz
  84619. coordination
  84620. chemistry
  84621. mangane
  84622. daves
  84623. daves
  84624. spectrometry
  84625. involatile
  84626. thermally
  84627. david
  84628. david
  84629. david
  84630. serge
  84631. claudine
  84632. gautheron
  84633. christine
  84634. enzymic
  84635. method
  84636. davide
  84637. davidj
  84638. davidovish
  84639. davidson
  84640. davidson
  84641. practical
  84642. aspects
  84643. photochemistry
  84644. davies
  84645. davies
  84646. conformations
  84647. nucleosides
  84648. nucleotides
  84649. davies
  84650. parrott
  84651. radicals
  84652. organic
  84653. synthesis
  84654. davies
  84655. david
  84656. aromatic
  84657. heterocyclic
  84658. chemistry
  84659. oxford
  84660. chemis
  84661. davies
  84662. geoffrey
  84663. green
  84664. richard
  84665. avermectins
  84666. milbemycin
  84667. davies
  84668. green
  84669. mingos
  84670. nucleophilic
  84671. addition
  84672. davies
  84673. stephen
  84674. donohoe
  84675. timothy
  84676. williams
  84677. jonathan
  84678. davis
  84679. davis
  84680. anthony
  84681. cholaphanes
  84682. steroids
  84683. structural
  84684. davis
  84685. anthony
  84686. cholaphaneset
  84687. steroids
  84688. asstructural
  84689. compo
  84690. davis
  84691. franklin
  84692. asymmetric
  84693. hydroxylation
  84694. davis
  84695. vistas
  84696. zeolite
  84697. molecular
  84698. sieve
  84699. catal
  84700. davis
  84701. michael
  84702. gilbert
  84703. brice
  84704. radical
  84705. actions
  84706. dawson
  84707. dawson
  84708. polymeric
  84709. aldrichimica
  84710. dawson
  84711. graham
  84712. williams
  84713. jonathan
  84714. catalytic
  84715. applications
  84716. dbu/dmso
  84717. dbu/dmso
  84718. promoted
  84719. dehydrobromination
  84720. dibromoolefins
  84721. ddathf
  84722. davis
  84723. anthony
  84724. cholaphaneset
  84725. steroids
  84726. asstructural
  84727. compo@
  84728. cleaning
  84729. oxidations
  84730. hydrogen
  84731. peroxide
  84732. 19931@
  84733. decompositions@
  84734. deficient@
  84735. dekker
  84736. delucchi@
  84737. dendrobates@
  84738. deoxygenation
  84739. phosphorus
  84740. reagents
  84741. heterocyclic
  84742. derivatives
  84743. deryagina
  84744. voronkov
  84745. korchevin
  84746. selenium
  84747. tellur@
  84748. design
  84749. deslongchamps
  84750. pierre
  84751. transannular
  84752. diels
  84753. alder
  84754. reaction
  84755. detection
  84756. quantitative
  84757. determination
  84758. aldehydes@
  84759. chemistry
  84760. longifolene
  84761. derivatives
  84762. development
  84763. ideas
  84764. concerning
  84765. mechanism
  84766. fischer@
  84767. developments
  84768. dewick
  84769. biosynthesis
  84770. shikimate
  84771. metabolites
  84772. natural
  84773. diacyl
  84774. dialkylation@
  84775. dialkyltriazenes
  84776. jerry
  84777. deciphering
  84778. information
  84779. content
  84780. polycy@
  84781. diastereofacial
  84782. selectivity
  84783. diels-alder
  84784. reactions
  84785. groot
  84786. jansen
  84787. verstegen
  84788. haaksma
  84789. swarts
  84790. reinhoudt
  84791. stability
  84792. reactivity
  84793. crown
  84794. keukeleire
  84795. denis
  84796. photochemical
  84797. strategies
  84798. kimpe
  84799. schamp
  84800. synthesis
  84801. alpha
  84802. halogenated
  84803. enami
  84804. kimpe
  84805. verhe
  84806. buyck
  84807. schamp
  84808. reactivity
  84809. halog
  84810. lucchi
  84811. ottorino
  84812. miotti
  84813. umberto
  84814. modena
  84815. giorgio
  84816. pummere
  84817. meijere
  84818. bonding
  84819. properties
  84820. cyclopropane
  84821. their
  84822. meijere
  84823. armin
  84824. wessjohann
  84825. ludger
  84826. tailoring
  84827. reactivity
  84828. violet
  84829. polyhalide
  84830. radical
  84831. anions
  84832. intermediates
  84833. deacetoxytaxol
  84834. deactivation
  84835. deacylation
  84836. deady
  84837. dealing
  84838. dealkoxycarbonylatio
  84839. dealkylation
  84840. dealkylations
  84841. deallyloxycarbonylat
  84842. deamination
  84843. cleaning
  84844. oxidations
  84845. hydrogen
  84846. peroxide
  84847. 19931
  84848. dearg
  84849. dearomatization
  84850. dearomatization
  84851. furan
  84852. structure
  84853. furan
  84854. complex
  84855. deazanucleosides
  84856. debenzhydrylation
  84857. debiak
  84858. deborah
  84859. debra
  84860. debreczy
  84861. debromination
  84862. debromoaplysin
  84863. decade
  84864. decades
  84865. decahydroquinolines
  84866. decane
  84867. decanes
  84868. decarbonylation
  84869. decarboxylation
  84870. decarboxylation
  84871. amino
  84872. acids
  84873. containing
  84874. three
  84875. decarboxylative
  84876. decarboxylution
  84877. decay
  84878. deciphering
  84879. deciphering
  84880. information
  84881. content
  84882. polycyclic
  84883. conjugated
  84884. decker
  84885. declercq
  84886. decoding
  84887. decomposition
  84888. decompositions
  84889. decoupling
  84890. dediazoniation
  84891. deepak
  84892. deerfield
  84893. deethylibophyllidine
  84894. nazarenko
  84895. pashkevich
  84896. ponomarev
  84897. iodoperf
  84898. deevi
  84899. deexcitation
  84900. defense
  84901. deferred
  84902. deferred
  84903. carbonylative
  84904. esterification
  84905. palladium
  84906. catal
  84907. defficient
  84908. defined
  84909. definite
  84910. defluorination
  84911. deformation
  84912. szafran
  84913. zofia
  84914. szafran
  84915. miroslaw
  84916. complexes
  84917. carboxylic
  84918. deganello
  84919. deganello
  84920. transition
  84921. metal
  84922. complexes
  84923. cyclic
  84924. polyolefin
  84925. degenerate
  84926. degenerate
  84927. carbocation
  84928. rearrangements
  84929. degenerate
  84930. carbonium
  84931. degenhardt
  84932. degl'innocenti
  84933. degradation
  84934. degradation
  84935. degradation
  84936. reactions
  84937. dehalogenation
  84938. dehmlow
  84939. dehmlow
  84940. dehmlow
  84941. phase
  84942. transfer
  84943. catalysis
  84944. monographs
  84945. dehmlow
  84946. dehmlow
  84947. phase
  84948. transfer
  84949. catalysis
  84950. dehydration
  84951. dehydrative
  84952. dehydro
  84953. dehydroacetic
  84954. dehydroacetic
  84955. triacetic
  84956. lactone
  84957. related
  84958. pyrone
  84959. dehydroamino
  84960. dehydrobromination
  84961. dehydrobromination
  84962. dibromoolefins
  84963. general
  84964. synthes
  84965. dehydrocarboranes
  84966. dehydrocyclization
  84967. dehydrogenase
  84968. dehydrogenation
  84969. dehydrogenative
  84970. dehydrogenative
  84971. coupling
  84972. reactions
  84973. hydrosilanes
  84974. dehydropeptides
  84975. dehydropyridinium
  84976. dehydropyrrolizidin
  84977. dehydroquinate
  84978. dejong
  84979. dekkerQ
  84980. dekker
  84981. delaude
  84982. delaude
  84983. lionel
  84984. laszlo
  84985. pierre
  84986. smith
  84987. keith
  84988. heightened
  84989. selectiv
  84990. delgado
  84991. delhi
  84992. delia
  84993. delia
  84994. thomas
  84995. warner
  84996. fused
  84997. pyrimidines
  84998. miscel
  84999. delivery
  85000. dellinger
  85001. delocalization
  85002. delocalized
  85003. delocalized
  85004. carbanions
  85005. synthesis
  85006. delong
  85007. deloux
  85008. deloux
  85009. laurent
  85010. srebnik
  85011. morris
  85012. asymmetric
  85013. boron
  85014. catalyzed
  85015. delpon
  85016. delta
  85017. delta-amino
  85018. delta-carbamoyloxy-a
  85019. delta-hydrogen
  85020. deltamethrinic
  85021. deluca
  85022. deluca
  85023. paaren
  85024. schnoes
  85025. vitamin
  85026. calcium
  85027. delucchi
  85028. delzenne
  85029. delzenne
  85030. organic
  85031. photochemical
  85032. imaging
  85033. systems
  85034. demand
  85035. demayo
  85036. demethoxy
  85037. demethylation
  85038. demillequand
  85039. demir
  85040. demir
  85041. ayhan
  85042. jeganathan
  85043. alwarsamy
  85044. selective
  85045. oxidation
  85046. demjanov
  85047. demmin
  85048. demonstration
  85049. demonstration
  85050. synthetic
  85051. power
  85052. oxazaborolidine
  85053. demonstration
  85054. synthetic
  85055. utility
  85056. generation
  85057. dempsey
  85058. demuth
  85059. demuth
  85060. martin
  85061. synthetic
  85062. aspects
  85063. oxadi
  85064. methane
  85065. dendrimers
  85066. dendrimers
  85067. arborols
  85068. cascade
  85069. molecules
  85070. breakthrough
  85071. dendrimers
  85072. generations
  85073. functional-groups
  85074. functio
  85075. dendritic
  85076. dendrobates
  85077. dendrobatid
  85078. dendrobatidae
  85079. denenmark
  85080. deneubourg
  85081. dengler
  85082. dengler
  85083. fontain
  85084. knauer
  85085. michael
  85086. stein
  85087. natalie
  85088. denholm
  85089. denice
  85090. deninno
  85091. deninno
  85092. michael
  85093. synthesis
  85094. glycosidation
  85095. acety
  85096. denis
  85097. denise
  85098. denisov
  85099. denisova
  85100. denitro
  85101. denitrogenation
  85102. dennis
  85103. denny
  85104. denopamine
  85105. denovo
  85106. density
  85107. deorazio
  85108. deoxy
  85109. deoxygemation
  85110. deoxygenated
  85111. deoxygenation
  85112. deoxygenation
  85113. alcohols
  85114. vicinal
  85115. diols
  85116. using
  85117. variety
  85118. deoxygenation
  85119. coordinated
  85120. sulfoxides
  85121. deoxygenation
  85122. phosphorus
  85123. reagents
  85124. heterocyclic
  85125. deoxygenations
  85126. deoxygenations
  85127. using
  85128. phosphorus
  85129. reagents
  85130. general
  85131. funct
  85132. deoxygenative
  85133. deoxygenative
  85134. coupling
  85135. amides
  85136. sm/smi2
  85137. system
  85138. deoxymannojirimycin
  85139. deoxypancratistatin
  85140. depaemelaere
  85141. dependence
  85142. dependencies
  85143. dependent
  85144. depoorter
  85145. deprotection
  85146. deprotection
  85147. dithianes
  85148. dichloro
  85149. dicyano
  85150. deprotection
  85151. arenesulfonamides
  85152. samarium
  85153. iodide
  85154. deprotonation
  85155. alkylation
  85156. alkyl
  85157. cyanides
  85158. under
  85159. sonochemica
  85160. deprotonations
  85161. depsipeptide
  85162. depuy
  85163. depuy
  85164. bierbaum
  85165. phase
  85166. reactions
  85167. organic
  85168. anions
  85169. deracemization
  85170. emization
  85171. highly
  85172. enantioselective
  85173. enolate
  85174. protonati
  85175. derek
  85176. dergachev
  85177. derik
  85178. deriv
  85179. derivation
  85180. derivativ
  85181. derivative
  85182. derivativesd
  85183. derivatives
  85184. derivatives
  85185. derivatives
  85186. aminomethyl
  85187. pyrrole
  85188. carboxylic
  85189. derivatives
  85190. diphosphonic
  85191. acids
  85192. synthesis
  85193. biological
  85194. derivatives
  85195. pyrrole
  85196. derivatives
  85197. monoperoxy
  85198. diperoxy
  85199. carbonic
  85200. acids
  85201. derivatives
  85202. peroxy
  85203. dicarbonic
  85204. acids
  85205. derivatives
  85206. telluric
  85207. derivatives
  85208. tellurous
  85209. derivatives
  85210. telluroxylic
  85211. ho-te-oh
  85212. derivatives
  85213. trivalent
  85214. phosphorus
  85215. synthesis
  85216. derivatization
  85217. derived
  85218. derkach
  85219. derry
  85220. deryagina
  85221. deryagina
  85222. voronkov
  85223. korchevin
  85224. selenium
  85225. tellur
  85226. desacetamido
  85227. desacetamidopyrimido
  85228. desbpande
  85229. descarboxamidopyrimi
  85230. descoles
  85231. descotes
  85232. describing
  85233. description
  85234. descriptions
  85235. descriptors
  85236. deselenenylation
  85237. deshong
  85238. desideno
  85239. designU
  85240. design
  85241. design
  85242. implementation
  85243. tactically
  85244. novel
  85245. strategies
  85246. design
  85247. synthesis
  85248. artificial
  85249. channels
  85250. design
  85251. synthesis
  85252. novel
  85253. chalcogen-containing
  85254. organic
  85255. design
  85256. concepts
  85257. developing
  85258. highly
  85259. efficient
  85260. chiral
  85261. bisph
  85262. design
  85263. amphoteric
  85264. bifunctional
  85265. ligands
  85266. enantiosele
  85267. design
  85268. antitumor
  85269. prodrugs
  85270. substrates
  85271. antibody-targete
  85272. design
  85273. chemically
  85274. robust
  85275. metallo-porphyrins
  85276. efficient
  85277. design
  85278. enediyne
  85279. prodrugs
  85280. design
  85281. synthesis
  85282. applications
  85283. oxygenated
  85284. chiral
  85285. design
  85286. synthesis
  85287. evaluation
  85288. functional
  85289. analogs
  85290. designed
  85291. gning
  85292. designs
  85293. desilva
  85294. desilyl
  85295. desilylation
  85296. desimoni
  85297. desio
  85298. desiraju
  85299. deslauriers
  85300. deslongchamps
  85301. deslongchamps
  85302. stereoelectronic
  85303. control
  85304. hydrolytic
  85305. react
  85306. deslongchamps
  85307. pierre
  85308. transannular
  85309. diels
  85310. alder
  85311. reaction
  85312. desmaele
  85313. desmurs
  85314. desmurs
  85315. roger
  85316. gerard
  85317. bernard
  85318. advances
  85319. organobrom
  85320. desongchamps
  85321. desorption
  85322. desoxoprosophylline
  85323. desoxoprosopinine
  85324. desponds
  85325. destabilised
  85326. destabilised
  85327. carbocations
  85328. destabilized
  85329. destabilized
  85330. carbocations
  85331. destabilizing
  85332. destomic
  85333. desulfonylation
  85334. desulfonylative
  85335. desulfonylative
  85336. transformation
  85337. reactions
  85338. arylsulfonyl
  85339. desulfurization
  85340. furization
  85341. organic
  85342. sulfur
  85343. compounds
  85344. mediated
  85345. desulfurization
  85346. raney
  85347. nickel
  85348. desulphurization
  85349. desvergne
  85350. detailed
  85351. detecting
  85352. detecting
  85353. ovalent
  85354. complexes
  85355. biological
  85356. macromolecules
  85357. detection
  85358. detection
  85359. quantitative
  85360. determination
  85361. aldehydes
  85362. detectors
  85363. determ
  85364. determinants
  85365. determination
  85366. determination
  85367. molecular
  85368. conformation
  85369. large
  85370. amplitude
  85371. determination
  85372. transition
  85373. state
  85374. geometries
  85375. restric
  85376. determinations
  85377. determinations
  85378. transition-state
  85379. geometries
  85380. endocyc
  85381. determine
  85382. determined
  85383. determining
  85384. determinmg
  85385. detlef
  85386. detoxin
  85387. detzer
  85388. deuchert
  85389. deuchert
  85390. hunig
  85391. multistage
  85392. organic
  85393. redox
  85394. systems
  85395. genera
  85396. deuchert
  85397. hunig
  85398. bifunctional
  85399. pyridines
  85400. relate
  85401. deuterium
  85402. aspects
  85403. longifolene
  85404. chemistry
  85405. example
  85406. another
  85407. chemistry
  85408. longifolene
  85409. derivatives
  85410. developement
  85411. developement
  85412. titanocene
  85413. catalyzed
  85414. enyne
  85415. cyclization
  85416. developement
  85417. copper
  85418. catalyzed
  85419. olefin
  85420. aziridination
  85421. developements
  85422. developing
  85423. developmen
  85424. development}
  85425. development
  85426. application
  85427. continuous
  85428. microwave
  85429. reacto
  85430. development
  85431. simple
  85432. procedure
  85433. synthesis
  85434. development
  85435. strategy
  85436. synthesis
  85437. unusual
  85438. development
  85439. carbene
  85440. complexes
  85441. reagents
  85442. development
  85443. ideas
  85444. concerning
  85445. mechanism
  85446. fischer
  85447. development
  85448. methodology
  85449. based
  85450. oxabicy
  85451. development
  85452. modified
  85453. chiral
  85454. dioxolane
  85455. biphosphine
  85456. ligands
  85457. development
  85458. reactivities
  85459. selectivities
  85460. stabil
  85461. development
  85462. synthetic
  85463. methodology
  85464. based
  85465. zirconium
  85466. development
  85467. organopalladium
  85468. chemistry
  85469. fundamental
  85470. development
  85471. copper
  85472. catalyzed
  85473. olefin
  85474. aziridination
  85475. developments
  85476. developments
  85477. opments
  85478. arylnitrene
  85479. chemistry
  85480. syntheses
  85481. mechanis
  85482. developments
  85483. cyclisation
  85484. reactions
  85485. developments
  85486. cyclization
  85487. reactions
  85488. developments
  85489. cycloproparene
  85490. chemistry
  85491. developments
  85492. chemistry
  85493. thiopyrans
  85494. selenopyrans
  85495. developments
  85496. incycloproparene
  85497. chemistry
  85498. review
  85499. strain
  85500. devens
  85501. devillers
  85502. devlin
  85503. devynck
  85504. dewar
  85505. dewar
  85506. michael
  85507. semiempirical
  85508. profiles
  85509. pathways
  85510. dewick
  85511. dewick
  85512. biosynthesis
  85513. shikimate
  85514. metabolites
  85515. dewick
  85516. biosynthesis
  85517. shikimate
  85518. metabolites
  85519. 199310
  85520. dewick
  85521. biosynthesis
  85522. shikimate
  85523. metabolites
  85524. natural
  85525. dewick
  85526. biosynthesis
  85527. shikimate
  85528. metabolites
  85529. natural
  85530. biochemistry
  85531. galactosidic
  85532. linkages
  85533. biochemistry
  85534. plant
  85535. galactomannans
  85536. deyrup
  85537. deyrup
  85538. aziridines
  85539. small
  85540. heterocycles
  85541. chemistry
  85542. chemistry
  85543. chalcones
  85544. related
  85545. compounds
  85546. dharanipragada
  85547. dhemistry
  85548. dhingra
  85549. polyalkali
  85550. metal
  85551. derivativ
  85552. heterofunctionally
  85553. polycarbanions
  85554. polycarbocations
  85555. polysulfanes
  85556. methane
  85557. photoisomerizations
  85558. di-pi-methane-like
  85559. di-pi-methane-like
  85560. photorearrangements
  85561. alpha
  85562. beta-unsatur
  85563. diacetate
  85564. diacetylenes
  85565. diacyl
  85566. diacyl
  85567. diacyl
  85568. peroxides
  85569. diacylimidazolidin
  85570. diacylimidazolidine
  85571. diacylmethylene
  85572. diacyltellurium
  85573. diacyltellurium
  85574. compounds
  85575. diagnosis
  85576. dialdehydes
  85577. dialdoses
  85578. dialkenyl
  85579. dialkoxy
  85580. dialkoxyamines
  85581. dialkoxycarbenium
  85582. dialkyl
  85583. dialkyl
  85584. hydrogen
  85585. phosphonates
  85586. structures
  85587. dialkyl
  85588. hydrog
  85589. dialkyl
  85590. hydrogen
  85591. phosphonates
  85592. substitution
  85593. reactions
  85594. dialkyl
  85595. peroxides
  85596. dialkylamide
  85597. dialkylamides
  85598. dialkylamino
  85599. dialkylamino-a
  85600. dialkylaminonitriles
  85601. dialkylaminopyridine
  85602. ylborane
  85603. dialkylboron
  85604. dialkylcobalt
  85605. dialkylcuprate
  85606. dialkylidenecycloalk
  85607. dialkyloxaziridines
  85608. dialkylperoxides
  85609. dialkylplatinum
  85610. dialkylsulfides
  85611. dialkyltriazenes
  85612. dialkyltriazenes
  85613. dialkylvinyl
  85614. dialkylvinylsulfoniu
  85615. dialkylzincs
  85616. dialkynyl
  85617. diallyl
  85618. diallylamines
  85619. diallylation
  85620. diallyldibutyltin
  85621. diamidides
  85622. diamines
  85623. diamino
  85624. diaminocyclohexane
  85625. diaminodicarboxylic
  85626. diaminodicarboxylic
  85627. acids
  85628. excluding
  85629. cystine
  85630. their
  85631. incorp
  85632. diaminonaphthalenes
  85633. diaminosulfoxonium
  85634. diaminothiophenes
  85635. diamondoid
  85636. diana
  85637. diane
  85638. dianhydro
  85639. dianion
  85640. dianionic
  85641. dianions
  85642. dianons
  85643. dianov
  85644. dianova
  85645. dianova
  85646. zabotina
  85647. compounds
  85648. dicoordinate
  85649. arsenic
  85650. diaryl
  85651. diaryl-37-dioxabicyc
  85652. diarylethylenes
  85653. diarylhepta
  85654. diarylmethanes
  85655. diaryltetrahydro
  85656. diarylureas
  85657. jerry
  85658. deciphering
  85659. information
  85660. content
  85661. polycy
  85662. jerry
  85663. molecular
  85664. orbital
  85665. calculations
  85666. using
  85667. chemical
  85668. jerry
  85669. setting
  85670. benzenoids
  85671. order
  85672. chemistry
  85673. jerry
  85674. current
  85675. status
  85676. isomer
  85677. enumeration
  85678. diastereo
  85679. diastereo
  85680. enantioselective
  85681. synthesis
  85682. oudemansin
  85683. diastereo
  85684. regioselectivity
  85685. reactions
  85686. dilithiat
  85687. diastereocontrol
  85688. diastereocontrol
  85689. highly
  85690. enantioselective
  85691. carbon
  85692. hydrogen
  85693. diastereocontrol
  85694. highly
  85695. enantioselective
  85696. carbon-hydrogen
  85697. diastereocontrol
  85698. opening
  85699. acceptor
  85700. donor
  85701. cyclop
  85702. diastereofacial
  85703. diastereofacial
  85704. discrimination
  85705. reaction
  85706. chiral
  85707. diastereofacial
  85708. selectivity
  85709. diels
  85710. alder
  85711. reaction
  85712. diastereofacial
  85713. selectivity
  85714. diels-alder
  85715. reaction
  85716. diastereofacial
  85717. selectivity
  85718. diels-alder
  85719. reactions
  85720. diastereogenic
  85721. diastereogenic
  85722. addition
  85723. crotylmetal
  85724. compounds
  85725. aldehyde
  85726. diastereoisomers
  85727. diastereomeric
  85728. diastereomerically
  85729. diastereomers
  85730. diastereomic
  85731. diastereoselection
  85732. diastereoselectiveI
  85733. cente
  85734. diastereoselective
  85735. cycloaddition
  85736. phenylthiocyclopro
  85737. diastereoselective
  85738. addition
  85739. allyltriphenyl
  85740. stannane
  85741. diastereoselective
  85742. addition
  85743. organometallic
  85744. reagents
  85745. diastereoselective
  85746. additions
  85747. using
  85748. cameo
  85749. cram's
  85750. asymmetI
  85751. diastereoselective
  85752. aldol
  85753. allylsilane
  85754. addition
  85755. reactions
  85756. diastereoselective
  85757. enantioselective
  85758. synthesis
  85759. diastereoselective
  85760. formation
  85761. carbene
  85762. insertions
  85763. diastereoselective
  85764. carbometalation
  85765. vinylmetals
  85766. diastereoselective
  85767. conjugate
  85768. additions
  85769. reactions
  85770. lithia
  85771. diastereoselective
  85772. control
  85773. opening
  85774. activated
  85775. cyclo
  85776. diastereoselective
  85777. cycloisomerizations
  85778. enediynes
  85779. diastereoselective
  85780. cyclopropanation
  85781. chiral
  85782. allylic
  85783. alcoho
  85784. diastereoselective
  85785. cyclopropanations
  85786. chiral
  85787. bicyclic
  85788. diastereoselective
  85789. diels
  85790. alder
  85791. cycloadditions
  85792. chiral
  85793. diastereoselective
  85794. diels
  85795. alder
  85796. reactions
  85797. using
  85798. furan
  85799. substit
  85800. diastereoselective
  85801. reaction
  85802. 3-formyl-d2-isoxazol
  85803. diastereoselective
  85804. heteroatom
  85805. directed
  85806. conjugate
  85807. addition
  85808. diastereoselective
  85809. intramolecular
  85810. bis-silylation
  85811. carbon
  85812. diastereoselective
  85813. additions
  85814. using
  85815. cameo
  85816. cram's
  85817. asymmet@
  85818. diastereoselective
  85819. diels-alder
  85820. reactions
  85821. cyclic
  85822. vinylcar@
  85823. diastereoselective
  85824. oxidation
  85825. substituted
  85826. dithiolan
  85827. diastereoselectiviti@
  85828. francois
  85829. cyclophanes
  85830. royal
  85831. society
  85832. chemistry
  85833. diels
  85834. diels-alder
  85835. cycloaddition
  85836. unsaturated
  85837. sugars
  85838. stereocontro@
  85839. dienes
  85840. dietmar@
  85841. difunctionalization
  85842. dihydrofurans
  85843. diimide@
  85844. dimeric@
  85845. dimethylimidazolidin@
  85846. diorganotellurium
  85847. compounds
  85848. r-te-r
  85849. dioxiranes
  85850. dipolaires
  85851. dipyridine@
  85852. direct
  85853. formation
  85854. haloaryl
  85855. copper
  85856. nucleophiles
  85857. haloio@
  85858. directed
  85859. ortho
  85860. metalation
  85861. cross
  85862. coupling
  85863. connections
  85864. nickel
  85865. directional@
  85866. disconnection@
  85867. displacement
  85868. disubstituted@
  85869. dithiatriazines
  85870. divergent
  85871. dl-b-amyrin@
  85872. dolphin
  85873. porphyrins
  85874. physical
  85875. chemistry
  85876. diastereoselective
  85877. oxidation
  85878. substituted
  85879. dithiolan
  85880. diastereoselective
  85881. oxidation
  85882. substituted
  85883. thietanes
  85884. diastereoselective
  85885. oxidation
  85886. sulfides
  85887. sulfoxides
  85888. synth
  85889. diastereoselective
  85890. radical
  85891. bromination
  85892. dihydro
  85893. diastereoselective
  85894. reactions
  85895. sulfoximines
  85896. diastereoselective
  85897. reduction
  85898. carbon
  85899. nitrogen
  85900. double
  85901. diastereoselective
  85902. synthesis
  85903. cis-12-dialkenylcycl
  85904. diastereoselectivean
  85905. diastereoselectivity
  85906. diastereoselectivity
  85907. insertion
  85908. reactions
  85909. rhodi
  85910. diastereoselectivity
  85911. insertion
  85912. reactions
  85913. rhodiu
  85914. diastereoselectivity
  85915. paterno
  85916. buchi
  85917. reaction
  85918. diasterofacial
  85919. diatomic
  85920. diaza
  85921. diazabicyclo
  85922. diazabicycloundecene
  85923. diazadiene
  85924. diazadiphosphetidine
  85925. diazaquinone
  85926. diazaspirocycloalkan
  85927. diazaspirocycloalkan
  85928. diazene
  85929. diazenes
  85930. diazenium
  85931. diazepines
  85932. diazepinium
  85933. diazetidines
  85934. diazides
  85935. diazinenucleus
  85936. diazines
  85937. diazinodiazines
  85938. diaziridines
  85939. diaziridinimines
  85940. diaziridinones
  85941. diazirine
  85942. diazirines
  85943. diazo
  85944. diazo
  85945. compounds
  85946. diazo
  85947. compounds
  85948. properties
  85949. synthesis
  85950. diazo-b
  85951. diazo-carbonyl
  85952. diazoacetamides
  85953. diazoacetate
  85954. diazoacetates
  85955. diazoacetoacetates
  85956. diazoalkane
  85957. diazoalkanes
  85958. diazoamides
  85959. diazoazoles
  85960. diazocarbonyl
  85961. diazocines
  85962. diazoesters
  85963. diazoimides
  85964. diazoketone
  85965. diazoketone
  85966. cyclizations
  85967. their
  85968. amplication
  85969. synthesis
  85970. diazoketones
  85971. diazolakanes
  85972. diazoles
  85973. diazomethane
  85974. diazomethanes
  85975. diazonacetate
  85976. diazonamide
  85977. diazonium
  85978. diazoniunn
  85979. diazotetraphenylcycl
  85980. diazotization
  85981. dibah
  85982. dibasic
  85983. dibenzazonine
  85984. dibenzo
  85985. dibenzo
  85986. pyridines
  85987. phenanthridines
  85988. dibenzo
  85989. pyrylium
  85990. salts
  85991. dibenzo
  85992. thiopyrylium
  85993. salts
  85994. dibenzo-18-crown-6
  85995. dibenzofurans
  85996. dibenzothiazepines
  85997. dibenzothiophenes
  85998. dibenzoxazepines
  85999. dibenzoyl
  86000. dibenzylamino
  86001. dibismuthines
  86002. diborane
  86003. diboron
  86004. dibromide
  86005. dibromides
  86006. dibromo
  86007. dibromoalk
  86008. dibromoalkenes
  86009. dibromocompounds
  86010. dibromodifluorometha
  86011. dibromoethane
  86012. dibromoolefins
  86013. dicarba
  86014. dicarbaldehydes
  86015. dicarbanion
  86016. dicarbonic
  86017. dicarbonic
  86018. derivatives
  86019. cyano
  86020. function
  86021. dicarbonic
  86022. derivatives
  86023. isocyanate
  86024. isothiocyanat
  86025. dicarbonic
  86026. derivatives
  86027. orthocarbonic
  86028. function
  86029. dicarbonic
  86030. derivatives
  86031. simple
  86032. carbonic
  86033. functio
  86034. dicarbonitrile
  86035. dicarbonyl
  86036. dicarbonylcyclopenta
  86037. dicarbonyls
  86038. dicarboxylates
  86039. dicarboxylic
  86040. dicationic
  86041. dications
  86042. dichlorine
  86043. dichloro
  86044. dichloroacetic
  86045. dichlorobut
  86046. dichlorocarbene
  86047. dichlorodi
  86048. dichlorodicyanoquino
  86049. dichloroethenes
  86050. dichlorofluoroalkane
  86051. dichloroiodate
  86052. dichloromethane
  86053. dichloromethyl
  86054. dichloromethyl
  86055. dimethylsilyl
  86056. group
  86057. hydroxymethylidene
  86058. dichloromethylboroni
  86059. dichloromethyleneamm
  86060. dichotomies
  86061. dichotomous
  86062. dichotomy
  86063. dichotomy
  86064. addition
  86065. carbon
  86066. centered
  86067. radicals
  86068. dichroism
  86069. dichromium
  86070. dickinson
  86071. microbial
  86072. pyran
  86073. dihydropyran
  86074. dickson
  86075. dicoordinate
  86076. dicots
  86077. dictionary
  86078. dictyopterene
  86079. dicyanides
  86080. dicyano
  86081. dicyanoanthracene
  86082. dicyanoethylenes
  86083. dicyanomethylidene
  86084. dicyanoquinone
  86085. dicyclo
  86086. dicyclohexyliodobora
  86087. dicyclopentadie
  86088. dideaza
  86089. didehydro
  86090. didehydropiperidine
  86091. dideoxy
  86092. dideoxyfuranoses
  86093. didier
  86094. die1s
  86095. dieckmann
  86096. diederich
  86097. diederich
  86098. isaacs
  86099. philp
  86100. synthesis
  86101. structures
  86102. proper
  86103. diederich
  86104. francois
  86105. cyclophanes
  86106. royal
  86107. society
  86108. chemistry
  86109. diederich
  86110. francois
  86111. smithrud
  86112. david
  86113. sanford
  86114. elizabeth
  86115. diederich
  86116. francois
  86117. whetten
  86118. robert
  86119. beyond
  86120. higher
  86121. diegoP
  86122. diekson
  86123. dielectric
  86124. dielsw
  86125. diels
  86126. diels
  86127. alder
  86128. reactions
  86129. transient
  86130. thionitrosoar
  86131. diels
  86132. alder
  86133. reaction
  86134. triazine
  86135. aldehyde
  86136. enamine
  86137. diels
  86138. alder
  86139. reactions
  86140. azadienes
  86141. diels
  86142. alder
  86143. reactions
  86144. azadienes
  86145. heterocycles
  86146. containi
  86147. diels
  86148. alder
  86149. reactions
  86150. cyclopropenone
  86151. ketals
  86152. concise
  86153. diels
  86154. alder
  86155. reactivity
  86156. vinylsulfoxyallenes
  86157. diels
  86158. alder
  86159. addition
  86160. retroaddition
  86161. cyclopentadie
  86162. diels-ald
  86163. diels-alder
  86164. diels-alder
  86165. cycloaddition
  86166. unsaturated
  86167. sugars
  86168. stereocontro
  86169. diels-alder
  86170. cycloadditions
  86171. 2-pyrones
  86172. 2-pyridones
  86173. diels-alder
  86174. reactions
  86175. azadienes
  86176. diels-alder
  86177. reactions
  86178. cycloalkenones
  86179. organic
  86180. synthesis
  86181. diels-alder
  86182. reactions
  86183. heterocyclic
  86184. azadienes
  86185. development
  86186. dienals
  86187. diene
  86188. diene
  86189. synthesis
  86190. boronate
  86191. fragmentation
  86192. diene
  86193. synthesis
  86194. nitro
  86195. compounds
  86196. diene-dienophile
  86197. diene/diene
  86198. dienediolates
  86199. dienediyne
  86200. dienes
  86201. dienes
  86202. diels-alder
  86203. reaction
  86204. dienic
  86205. dienol
  86206. dienolate
  86207. dienols
  86208. dienone
  86209. dienone-phenol
  86210. dienone-phenol
  86211. rearrangements
  86212. related
  86213. reactions
  86214. dienones
  86215. dienophile
  86216. dienophiles
  86217. dienophilic
  86218. dienophilic
  86219. reactivity
  86220. cycloadditions
  86221. dienopyranosid
  86222. dienopyranosides
  86223. dienst
  86224. dienyl
  86225. dienylic
  86226. dienylsiloxanes
  86227. dienynes
  86228. diepicastanospermine
  86229. diepoxides
  86230. diepoxybutane
  86231. diesters
  86232. diethers
  86233. diethienylalkanes
  86234. diethyl
  86235. diethylaluminum
  86236. diethylaminosulfur
  86237. diethylazodicarboxyl
  86238. diethylzinc
  86239. dietmar
  86240. dietrich
  86241. dietrich
  86242. buchecker
  86243. sauvage
  86244. synthetic
  86245. molecular
  86246. knots
  86247. dietz
  86248. differding
  86249. difference
  86250. differences
  86251. different
  86252. different
  86253. transition
  86254. structures
  86255. wittig
  86256. rearrangements
  86257. differential
  86258. differentially
  86259. differentiating
  86260. differentiation
  86261. hydroxyl
  86262. goups
  86263. regioselecti
  86264. difficult
  86265. difficulties
  86266. diffraction
  86267. diffractometric
  86268. diffusing
  86269. diffusion
  86270. difluoride
  86271. difluoro
  86272. difluoroalkyl
  86273. difluoroallene
  86274. difluorocarbene
  86275. difluorocyclohexane
  86276. difluorocyclopropane
  86277. difluoroiodomethane
  86278. difluoroiodomethane
  86279. practical
  86280. synthesis
  86281. reaction
  86282. difunctional
  86283. difunctionality
  86284. difunctionalization
  86285. difunctionalization
  86286. digonal
  86287. dihalides
  86288. dihalo
  86289. dihaloalkyl
  86290. dihaloboranes
  86291. dihalocarbene
  86292. dihalocyclopropanes
  86293. dihalocyclopropenes
  86294. dihalogenocarbene
  86295. dihetera
  86296. diheteroaryl
  86297. diheteroaryl
  86298. peroxides
  86299. diheterophospholans
  86300. diheterophosphorinan
  86301. diheterosubstituted
  86302. diheterosubstituted
  86303. ketenes
  86304. thioketenes
  86305. ketenimines
  86306. dihydro
  86307. dihydro-12-diazetes
  86308. dihydro-13-diazetes
  86309. dihydroanthracene
  86310. dihydroanthracenes
  86311. dihydrobenzenes
  86312. dihydrobenzofurans
  86313. dihydrobenzopyrans
  86314. dihydrobenzothiophen
  86315. dihydrocodeinone
  86316. dihydrofolate
  86317. dihydrofur
  86318. dihydrofuraldehydes
  86319. dihydrofuran
  86320. dihydrofuranones
  86321. dihydrofurans
  86322. dihydrofurans
  86323. dihydrogen
  86324. dihydroisocoumarins
  86325. dihydroisoquinolines
  86326. dihydroisoxazoles
  86327. dihydromahubanolide
  86328. dihydronaphthalenes
  86329. dihydropentalenes
  86330. dihydrophenanthrenes
  86331. dihydrophenophosphaz
  86332. dihydropseudopteroli
  86333. dihydropyran
  86334. dihydropyran-2-ones
  86335. dihydropyranaldehyde
  86336. dihydropyranones
  86337. dihydropyrans
  86338. dihydropyrenes
  86339. dihydropyridin
  86340. dihydropyridine
  86341. dihydropyridines
  86342. dihydropyrimidines
  86343. dihydropyrones
  86344. dihydrosesamin
  86345. dihydrothiazine
  86346. dihydrothiazolo
  86347. dihydrothiophene-11
  86348. dihydrothiophenes
  86349. dihydroxy
  86350. dihydroxyamides
  86351. dihydroxyethylene
  86352. dihydroxylation
  86353. rrolizidi
  86354. dihyroxylation
  86355. diimide
  86356. diimides
  86357. diimine
  86358. diimines
  86359. diiodide
  86360. diiodine
  86361. diiodoacetylene
  86362. diiodomethane
  86363. diiodosamarium
  86364. diiodosamarium
  86365. catalyst
  86366. precursor
  86367. diels
  86368. alder
  86369. diisobutylaluminium
  86370. diisobutylaluminum
  86371. diisocyanatocarbodii
  86372. diisopinocampheyl
  86373. diisopinocampheylbor
  86374. diisopropoxytitanium
  86375. llidene-a
  86376. diketene
  86377. diketene
  86378. leading
  86379. references
  86380. diketo
  86381. diketonates
  86382. diketone
  86383. diketones
  86384. dilip
  86385. dilithiated
  86386. dilithioalkylamines
  86387. dilling
  86388. dilute
  86389. dilution
  86390. dilworth
  86391. dimaio
  86392. dimension
  86393. dimensional
  86394. dimensionally
  86395. dimensions
  86396. dimer
  86397. dimeric
  86398. dimerisation
  86399. dimerization
  86400. dimerization
  86401. cycloproparenes
  86402. silver
  86403. dimers
  86404. dimetal
  86405. dimetallated
  86406. dimetallation
  86407. dimetalled
  86408. dimetallic
  86409. dimethoxymethane
  86410. dimethyl
  86411. dimethyl
  86412. methoxycarbonyl
  86413. bicyclo
  86414. 2.2.1
  86415. dimethylamino
  86416. dimethylaminoethyl
  86417. dimethylbenzofurans
  86418. dimethylbicyclo
  86419. dimethylcuprate
  86420. dimethylcyclopentane
  86421. dimethylcyclopropyl
  86422. dimethyldioxirane
  86423. dimethyldioxirane
  86424. epoxidation
  86425. alkenes
  86426. bearing
  86427. electro
  86428. dimethyldioxirane
  86429. epoxidation
  86430. phosphates
  86431. dimethylenecyclobute
  86432. dimethylenecyclobute
  86433. benzocyclobutadiene
  86434. benzodicyclobutadie
  86435. dimethylhydrazone
  86436. dimethylhydrazones
  86437. dimethylimidazolidin
  86438. dimethylisoxazole
  86439. dimethyloctane
  86440. dimethyloxirane
  86441. dimethylpentadecan
  86442. dimethylphenylpyrazo
  86443. dimethylphenylsilyl
  86444. dimethylsilyl
  86445. dimethylsulfide
  86446. dimethylsulfonium
  86447. dimethylsulfoxonium
  86448. dimethylsulphonium
  86449. dimolybdenum
  86450. dimroth
  86451. dinculescu
  86452. dinitro
  86453. dinitrogen
  86454. dinitrogen
  86455. fixation
  86456. solution
  86457. presence
  86458. dinitrophenylhydrazo
  86459. dinitrospiropentene
  86460. dinoflagellate
  86461. dinuclear
  86462. dinucleophiles
  86463. dinucleotide
  86464. dioate
  86465. diolefin
  86466. diolefin
  86467. complexes
  86468. useful
  86469. versatile
  86470. tools
  86471. organi
  86472. diols
  86473. diones
  86474. diorganotellurium
  86475. diorganotellurium
  86476. compounds
  86477. r-te-r
  86478. diorganotellurium
  86479. compounds
  86480. r-te-r
  86481. diorganotellurium
  86482. cyamide
  86483. salts
  86484. diorganotellurium
  86485. oxides
  86486. their
  86487. derivatives
  86488. diorganotetroxides
  86489. diorganotrioxides
  86490. diorganozinc
  86491. diorganozincs
  86492. dioxabicyclo
  86493. dioxaborinanyl
  86494. dioxaborolidines
  86495. dioxacyclanes
  86496. dioxan
  86497. dioxane
  86498. dioxaspiro
  86499. dioxaspirodecanes
  86500. dioxatrinanes
  86501. dioxaza
  86502. dioxazoles
  86503. dioxazoles
  86504. oxathiazoles
  86505. dithiazoles
  86506. dioxene
  86507. dioxepinone
  86508. dioxetane
  86509. dioxetanes
  86510. dioxetanes
  86511. alpha-peroxy
  86512. lactones
  86513. 4-membered
  86514. cyclic
  86515. dioxide
  86516. dioxides
  86517. dioximes
  86518. dioxin
  86519. dioxirane
  86520. dioxirane
  86521. mediated
  86522. alkene
  86523. epoxidation
  86524. review
  86525. dioxiranes
  86526. dioxiranes
  86527. dioxiranes
  86528. 3-membered
  86529. cyclic
  86530. dioxiranes
  86531. class
  86532. powerful
  86533. oxidants
  86534. dioxiranes
  86535. oxidation
  86536. chemistry
  86537. dioxoketene
  86538. dioxol
  86539. dioxolan
  86540. dioxolane
  86541. dioxolanes
  86542. dioxole
  86543. dioxoles
  86544. dioxoles
  86545. oxathiole
  86546. dioxygen
  86547. dioxygenases
  86548. dioxygenation
  86549. dipent
  86550. dipent
  86551. acetals
  86552. acetalization
  86553. agents
  86554. dipeptide
  86555. tides
  86556. diperoxy
  86557. diphenyl
  86558. diphenylacetylene
  86559. diphenylamine
  86560. diphenylcarbene
  86561. diphenylcuprate
  86562. diphenylmethoxy
  86563. diphenylphenoxide
  86564. diphenylphosphino
  86565. diphenylphosphinoyl
  86566. diphenylpolyene
  86567. diphenylsulfilimines
  86568. diphenyltin
  86569. diphosphazenes
  86570. diphosphenes
  86571. diphosphine
  86572. diphosphines
  86573. diphosphonic
  86574. diplatinum
  86575. dipolaires
  86576. dipolaires
  86577. dipolar
  86578. cycloaddition
  86579. cyclic
  86580. rhodium
  86581. carbenoids
  86582. dogona
  86583. dipolar
  86584. cycloaddition
  86585. rhodium
  86586. carbenoids
  86587. vinyl
  86588. ester
  86589. dipolar
  86590. cycloadditions
  86591. nitrones
  86592. vinyl
  86593. ethers
  86594. dipolar
  86595. cycloadditions
  86596. monofunctional
  86597. allenes
  86598. dipolarophile
  86599. dipolarophiles
  86600. dipolarophilic
  86601. dipole
  86602. dipole
  86603. stabilized
  86604. carbanions
  86605. dipole
  86606. stabilized
  86607. carbanions
  86608. novel
  86609. useful
  86610. intermediates
  86611. dipole-stabilized
  86612. dipole-stabilized
  86613. carbanions
  86614. novel
  86615. useful
  86616. intermediates
  86617. dipoles
  86618. diprotected
  86619. dipyridine
  86620. dipyrroles
  86621. diquinane
  86622. diradical
  86623. diradicals
  86624. direct
  86625. direct
  86626. amino
  86627. crotylsilylation
  86628. achiral
  86629. acetals
  86630. aldehyd
  86631. direct
  86632. highly
  86633. enantioselective
  86634. synthesis
  86635. ferrocenes
  86636. carboxymethylation
  86637. direct
  86638. conversion
  86639. esters
  86640. secondary
  86641. amides
  86642. using
  86643. direct
  86644. coupling
  86645. functionalized
  86646. organolithium
  86647. compounds
  86648. direct
  86649. effects
  86650. allylic
  86651. benzylic
  86652. polymetalations
  86653. direct
  86654. elaboration
  86655. complex
  86656. polyquinanes
  86657. through
  86658. 2-fold
  86659. direct
  86660. enantioselective
  86661. synthesis
  86662. diols
  86663. direct
  86664. evidence
  86665. oxocarbenium
  86666. intermediate
  86667. direct
  86668. formation
  86669. haloaryl
  86670. copper
  86671. nucleophiles
  86672. haloio
  86673. direct
  86674. n-alkyl
  86675. azidonation
  86676. n-dialkylarylamines
  86677. direct
  86678. polycondensation
  86679. direct
  86680. sulfonation
  86681. aromatic
  86682. hydrocarbons
  86683. their
  86684. haloge
  86685. direct
  86686. synthesis
  86687. fused
  86688. bicyclic
  86689. g-butyrolactones
  86690. directable
  86691. directed
  86692. directed
  86693. undirected
  86694. syntheses
  86695. novel
  86696. organic
  86697. compounds
  86698. directed
  86699. lithiation
  86700. aromatic
  86701. teriary
  86702. amides
  86703. evolving
  86704. directed
  86705. lithiations
  86706. effect
  86707. varying
  86708. directing
  86709. group
  86710. directed
  86711. macrocyclisation
  86712. reactions
  86713. directed
  86714. metalation
  86715. deficient
  86716. azaaromatics
  86717. strategies
  86718. directed
  86719. ortho
  86720. metalation
  86721. cross
  86722. coupling
  86723. connections
  86724. nickel
  86725. directed
  86726. ortho
  86727. metalation
  86728. mediated
  86729. introduction
  86730. regiospeci
  86731. directed
  86732. ortho
  86733. metalation
  86734. tertiary
  86735. amide
  86736. o-carbamate
  86737. directed
  86738. regio
  86739. stereoselective
  86740. nickel
  86741. catalyzed
  86742. addition
  86743. directed
  86744. stereoselectivity
  86745. alkaloid
  86746. synthesis
  86747. directedstereoselect
  86748. directing
  86749. directing
  86750. effect
  86751. dimethylimidazolidin
  86752. ortho
  86753. lithiat
  86754. directing
  86755. tandem
  86756. catalyzed
  86757. reactions
  86758. approach
  86759. furan
  86760. direction
  86761. ctional
  86762. directionality
  86763. directionality
  86764. organic
  86765. reactions
  86766. solution
  86767. directions
  86768. directive
  86769. directly
  86770. director
  86771. directors
  86772. dirhodium
  86773. dirks
  86774. disaccharide
  86775. disaccharides
  86776. disappearance
  86777. discipline
  86778. disciplines
  86779. discodermolide
  86780. discoderolide
  86781. disconnection
  86782. discotic
  86783. discovered
  86784. discoveries
  86785. discoveries
  86786. missed
  86787. discoveries
  86788. creativity
  86789. influence
  86790. discoverym
  86791. discovery
  86792. development
  86793. anthracycline
  86794. antitumour
  86795. antibi
  86796. discovery
  86797. synthesis
  86798. common
  86799. natural
  86800. hydroporphyri
  86801. discriminate
  86802. discriminating
  86803. discrimination
  86804. discriminations
  86805. discriminatively
  86806. discriminatory
  86807. discriminatory
  86808. interactions
  86809. between
  86810. chiral
  86811. molecules
  86812. discuss
  86813. disease
  86814. diselenides
  86815. dishong
  86816. disilene
  86817. disilene
  86818. silylene
  86819. additions
  86820. double
  86821. bonds
  86822. alken
  86823. disilenes
  86824. disodium
  86825. disodium
  86826. tetracarbonylferrate
  86827. transition
  86828. metal
  86829. analog
  86830. dison
  86831. disparlure
  86832. dispiroketals
  86833. dispiroketals
  86834. synthesis
  86835. further
  86836. reactions
  86837. dispoke
  86838. displacement
  86839. displacement
  86840. displacement
  86841. aliphatic
  86842. nitro
  86843. groups
  86844. carbon
  86845. heteroa
  86846. displacement
  86847. reactions
  86848. phosphorus
  86849. compounds
  86850. their
  86851. displacements
  86852. displayed
  86853. dispoke
  86854. disposal
  86855. disproof
  86856. disproportionation
  86857. dissection
  86858. disseminated
  86859. dissociation
  86860. dissociative
  86861. dissociative
  86862. pathways
  86863. substitution
  86864. silicon
  86865. solution
  86866. dissolving
  86867. dissymmetric
  86868. distance
  86869. distannanes
  86870. distannoxanes
  86871. distant
  86872. distibines
  86873. distillation
  86874. distinguishing
  86875. distinguishing
  86876. between
  86877. concerted
  86878. nonconcerted
  86879. eliminatio
  86880. distiniction
  86881. distiniction
  86882. between
  86883. polar
  86884. electron
  86885. transfer
  86886. routes
  86887. distorted
  86888. distortion
  86889. distortions
  86890. distortive
  86891. distribution
  86892. distributions
  86893. disubstituted
  86894. disulfide
  86895. disulfide
  86896. dications
  86897. cyclic
  86898. bis-sulfides
  86899. disulfides
  86900. disulfoxides
  86901. disulphide
  86902. ditchfield
  86903. ditellurium
  86904. diterpene
  86905. diterpenoid
  86906. diterpenoid
  86907. alkaloids
  86908. diterpenoidsZ
  86909. dithiadiazoles
  86910. dithiadiazoles
  86911. family
  86912. radicals
  86913. dithiametacyclophane
  86914. dithian
  86915. dithiane
  86916. dithianes
  86917. dithiatriazines
  86918. dithiatriazines
  86919. dithiazol
  86920. dithiazoles
  86921. dithiazolium
  86922. dithietane
  86923. dithiin
  86924. dithiins
  86925. dithiirane
  86926. dithio
  86927. dithioacetal
  86928. dithioacetals
  86929. dithiocarbamate
  86930. dithiocarbolcylic
  86931. dithiocarbonates
  86932. dithiocarboxylic
  86933. dithiocarboxylic
  86934. acids
  86935. dithiocarboxylic
  86936. salts
  86937. ester
  86938. dithioethene
  86939. dithioketals
  86940. dithiol
  86941. dithiolan
  86942. dithiolanes
  86943. dithiolate
  86944. dithiole
  86945. dithiolene
  86946. dithiolium
  86947. dithionite
  86948. dithioperoxyesters
  86949. dition
  86950. ditopic
  86951. dittmer
  86952. dittmer
  86953. chemistry
  86954. thiacyclobutenes
  86955. thietes
  86956. their
  86957. dittrich
  86958. ditungsten
  86959. divalent
  86960. divalent
  86961. samarium
  86962. compounds
  86963. perspectives
  86964. organic
  86965. chemist
  86966. divalent
  86967. silicon
  86968. intermediates
  86969. divergent
  86970. divergent
  86971. divergent
  86972. mechanisms
  86973. dealkoxycarbonylatio
  86974. diverse
  86975. diversely
  86976. diversity
  86977. reaction
  86978. modes
  86979. anionic
  86980. cationic
  86981. divinyl
  86982. divinyl
  86983. disulfides
  86984. synthesis
  86985. properties
  86986. divinyl
  86987. sulfoxide
  86988. synthesis
  86989. properties
  86990. applications
  86991. divinylacetylene
  86992. divinylcyclopropane
  86993. divinylcyclopropane
  86994. rearrangement
  86995. divinylcyclopropanes
  86996. divinyltetramethyldi
  86997. division
  86998. dixneuf
  86999. diyls
  87000. diyne
  87001. diynes
  87002. dizinc
  87003. djerassi
  87004. djerassi
  87005. structure
  87006. biosynthesis
  87007. cyclopropa
  87008. djerassi
  87009. silva
  87010. christopher
  87011. sponge
  87012. sterols
  87013. origins
  87014. djerassi
  87015. steroids
  87016. possible
  87017. profiles
  87018. pathways
  87019. djuric
  87020. dl-21-oxogelsemine
  87021. dl-b-amyrin
  87022. dl-samaderin
  87023. dmit2
  87024. dmitrikov
  87025. dmowski
  87026. alkynyl
  87027. methoxy
  87028. hydroxycyclobutenone
  87029. cleavage
  87030. neocarzinostatin
  87031. chromophore
  87032. establishing
  87033. dna-esperamicin
  87034. dna-interactive
  87035. dobler
  87036. dobler
  87037. ionophores
  87038. their
  87039. structures
  87040. wiley
  87041. interscience
  87042. docetaxel
  87043. documentation
  87044. doddrell
  87045. dodecaboranes
  87046. dodecahedrane
  87047. dodecahedranes
  87048. dodecahedranes
  87049. allied
  87050. spherical
  87051. molecules
  87052. dodziuk
  87053. dodziuk
  87054. helena
  87055. unusual
  87056. saturated
  87057. hydrocarbons
  87058. interaction
  87059. doerig
  87060. doetz
  87061. dogadina
  87062. dogane
  87063. dogane
  87064. takabatake
  87065. bersohn
  87066. computer
  87067. executed
  87068. synthesis
  87069. dogmatism
  87070. dogonal
  87071. doherty
  87072. doherty
  87073. nancy
  87074. hoffmann
  87075. norris
  87076. transition
  87077. metal
  87078. fluoro
  87079. doing
  87080. dojin
  87081. dokichev
  87082. dolabellane
  87083. dolbier
  87084. dolbier
  87085. thermal
  87086. rearrangements
  87087. difluorocyclopr
  87088. dolbier
  87089. william
  87090. cycloadditions
  87091. allenes
  87092. reactions
  87093. dolbier
  87094. william
  87095. thermal
  87096. rearrangements
  87097. fluorine
  87098. containin
  87099. dolby
  87100. dole-23-quinodimetha
  87101. dolgoplosk
  87102. doller
  87103. dolling
  87104. dolphin
  87105. dolphin
  87106. porphyrins
  87107. structure
  87108. synthesis
  87109. dolphin
  87110. porphyrins
  87111. structure
  87112. synthesis
  87113. dolphin
  87114. porphyrins
  87115. physical
  87116. chemistry
  87117. dolphin
  87118. porphyrins
  87119. physical
  87120. chemistry
  87121. dolphin
  87122. porphyrins
  87123. chemical
  87124. chemistry
  87125. dolphin
  87126. paine
  87127. covalently
  87128. linked
  87129. dimeric
  87130. domain
  87131. dombek
  87132. dombivli
  87133. dombrovskii
  87134. dominant
  87135. domingo
  87136. dominguez
  87137. dominic
  87138. dominique
  87139. domino
  87140. domsch
  87141. don't
  87142. donal
  87143. donald
  87144. donaldson
  87145. donaruma
  87146. donating
  87147. dondoni
  87148. doney
  87149. donna
  87150. donohoe
  87151. donor
  87152. donor
  87153. acceptor
  87154. substituted
  87155. cyclopropanes
  87156. versatile
  87157. building
  87158. donor
  87159. substituted
  87160. furans
  87161. trifluoromethyl
  87162. ethylene
  87163. donor-acceptor
  87164. donor-acceptor-subst
  87165. donor-acceptor-subst
  87166. cyclopropanes
  87167. versatile
  87168. building
  87169. blocks
  87170. donor-acceptor-subst
  87171. cyclopropanes
  87172. fischer
  87173. carbene
  87174. compl
  87175. donors
  87176. dooseop
  87177. dopke
  87178. dordrecht
  87179. dorfman
  87180. dorfman
  87181. aleshkova
  87182. polimbetova
  87183. levina
  87184. petrov
  87185. dorigo
  87186. dorland
  87187. dornyei
  87188. dorofeenko
  87189. doron
  87190. doron'kin
  87191. doroshkevich
  87192. double
  87193. donor-acceptor-subst
  87194. cyclopropanes
  87195. versatile
  87196. building
  87197. blocks@
  87198. doorn@
  87199. double
  87200. doubly@
  87201. zhang
  87202. radical
  87203. mediated
  87204. expansion
  87205. drawing@
  87206. drimane@
  87207. duncan
  87208. duthaler
  87209. rudolf
  87210. recent
  87211. developments
  87212. stereoselective@
  87213. dynamics
  87214. dynemycin@
  87215. organomagnesium
  87216. rearrangements
  87217. 16131
  87218. advances
  87219. hecker
  87220. toxic
  87221. irritant
  87222. cocarcinogenic
  87223. diterpene
  87224. stanoeva
  87225. khaimova
  87226. heterocycl
  87227. compds
  87228. 1305@
  87229. ease@
  87230. echner@
  87231. edition
  87232. effect@
  87233. electro-organic
  87234. synthesis@
  87235. electrocyclic
  87236. electron
  87237. electron
  87238. transfer
  87239. reaction
  87240. organic
  87241. chemistry@
  87242. electronic
  87243. electrophile@
  87244. electrophilic
  87245. aminations
  87246. oxaziridines@
  87247. element
  87248. eliel
  87249. double
  87250. double
  87251. asymmetric
  87252. synthesis
  87253. strategy
  87254. stereo
  87255. double
  87256. asymmetric
  87257. synthesis
  87258. strategy
  87259. stereoche
  87260. double
  87261. calixarene
  87262. design
  87263. synthesis
  87264. properties
  87265. double
  87266. carbonylation
  87267. reactions
  87268. double
  87269. diastereoselectivity
  87270. dipolar
  87271. cycloadditions
  87272. double
  87273. enantioselective
  87274. transesterification
  87275. racemic
  87276. carbo
  87277. double
  87278. stereodifferentiatin
  87279. acid-promoted
  87280. mukaiyama
  87281. aldol
  87282. double
  87283. stereodifferentiatin
  87284. aldol
  87285. reactions
  87286. documentatio
  87287. double-bonded
  87288. double-bridged
  87289. double-calix
  87290. double-calix-crowns
  87291. double-calixarene
  87292. double-calixarene
  87293. design
  87294. synthesis
  87295. properties
  87296. doubleday
  87297. doublers
  87298. doubly
  87299. diastereoselective
  87300. iodolactonizations
  87301. olefin
  87302. doubly-annulated
  87303. doubly-crowned
  87304. dougherty
  87305. douglas
  87306. dover
  87307. zhang
  87308. radical
  87309. mediated
  87310. expansion
  87311. dower
  87312. dowle
  87313. dowle
  87314. davies
  87315. synthesis
  87316. synthetic
  87317. utility
  87318. doxorubicin
  87319. doxsee
  87320. doxsee
  87321. kenneth
  87322. mouser
  87323. farahi
  87324. judah
  87325. titanium
  87326. doyle
  87327. doyle
  87328. michael
  87329. chiral
  87330. catalysts
  87331. enantioselective
  87332. carben
  87333. dozin
  87334. drabowica
  87335. drabowicz
  87336. drabowicz
  87337. jozef
  87338. kielbasinski
  87339. piotr
  87340. lyzwa
  87341. piotr
  87342. stereoselecti
  87343. dragan
  87344. drake
  87345. dramatic
  87346. dramatic
  87347. increase
  87348. turnover
  87349. numbers
  87350. palladium-catalyzed
  87351. dramatic
  87352. titanium
  87353. alkoxide
  87354. effect
  87355. catalytic
  87356. enantiose
  87357. drauz
  87358. drenth
  87359. drenth
  87360. guidelines
  87361. publication
  87362. research
  87363. exper
  87364. drenth
  87365. kwart
  87366. kinetics
  87367. applied
  87368. organic
  87369. reactions
  87370. marce
  87371. drenth
  87372. nolte
  87373. iminomethylene
  87374. rigid
  87375. helical
  87376. drewes
  87377. drimane
  87378. drimanes
  87379. driven
  87380. driving
  87381. drone
  87382. drovinylation
  87383. drozd
  87384. drozdova
  87385. drueckhammer
  87386. drueckhammer
  87387. hennen
  87388. william
  87389. pederson
  87390. richard
  87391. drugn
  87392. druge
  87393. drugs
  87394. drury
  87395. dsis2
  87396. dual-action
  87397. dubac
  87398. dubois
  87399. dubois
  87400. jacques
  87401. emile
  87402. cosse
  87403. barbi
  87404. aliette
  87405. strain
  87406. release
  87407. dubonosov
  87408. ducep
  87409. duction
  87410. dudley
  87411. dueholm
  87412. dueholm
  87413. pedersen
  87414. dideoxyfuranoses
  87415. converg
  87416. duerr
  87417. duesler
  87418. dugas
  87419. dulcere
  87420. dumas
  87421. dumesic
  87422. dumont
  87423. duncan
  87424. duncan
  87425. dunitz
  87426. dunitz
  87427. analysis
  87428. structure
  87429. organic
  87430. molec
  87431. dunkin
  87432. dunkin
  87433. matrix
  87434. isolation
  87435. technique
  87436. applicatio
  87437. dunogues
  87438. dunsaturated
  87439. duocarmycin
  87440. duocarmycins
  87441. duocarmycins
  87442. class
  87443. sequence
  87444. selective
  87445. minor
  87446. duplex
  87447. dupont
  87448. duran
  87449. durckheimer
  87450. during
  87451. durkin
  87452. gleiter
  87453. spiroconjugation
  87454. 197817
  87455. angewandte
  87456. durst
  87457. durucasu
  87458. durucasu
  87459. chemistry
  87460. ddathf
  87461. dideaza
  87462. tetra
  87463. dustman
  87464. dutasta
  87465. duthaler
  87466. duthaler
  87467. rudolf
  87468. hafner
  87469. andreas
  87470. alsters
  87471. rothe
  87472. streit
  87473. duthaler
  87474. rudolf
  87475. hafner
  87476. andreas
  87477. chiral
  87478. titanium
  87479. complexes
  87480. duthaler
  87481. rudolf
  87482. recent
  87483. developments
  87484. stereoselective
  87485. duxbury
  87486. duxbury
  87487. debra
  87488. photochemistry
  87489. photophysics
  87490. duyck
  87491. dvorko
  87492. dvorko
  87493. ponomareva
  87494. verdazyl
  87495. method
  87496. study
  87497. dyamaev
  87498. dyatkin
  87499. dyatlovn
  87500. compounds
  87501. alkali
  87502. metal
  87503. anions
  87504. angewan
  87505. crown
  87506. cryptand
  87507. complexation
  87508. catio
  87509. quessy
  87510. erythrina
  87511. related
  87512. alkaloids
  87513. dykstra
  87514. dykstra
  87515. clifford
  87516. electrostatic
  87517. interaction
  87518. potentials
  87519. dynami
  87520. dynamic
  87521. dynamic
  87522. stereochemistry
  87523. 7-membered
  87524. rings
  87525. using
  87526. dynamical
  87527. dynamical
  87528. processes
  87529. crystalline
  87530. organometallic
  87531. complexes
  87532. dynamics
  87533. dynamics
  87534. dynamics
  87535. eight-membered
  87536. rings
  87537. cyclooctane
  87538. class
  87539. dynamics
  87540. flexible
  87541. triplet
  87542. biradicals
  87543. dynamics
  87544. solvent
  87545. exchange
  87546. organolithium
  87547. reagents
  87548. lithi
  87549. dynamycin
  87550. dynemicin
  87551. influence
  87552. solvation
  87553. dzhafarov
  87554. dzhafarov
  87555. retro
  87556. aldol
  87557. processes
  87558. steroid
  87559. chemistry
  87560. dzhamanbaev
  87561. dzhemilev
  87562. dziomko
  87563. rganomagnesium
  87564. rearrangements
  87565. 16131
  87566. advances
  87567. akgun
  87568. pindur
  87569. heterocyclic
  87570. chemica
  87571. ashby
  87572. laemmle
  87573. stereochemist
  87574. campaigne
  87575. schneller
  87576. synthesis
  87577. cyclization
  87578. atkins
  87579. conformations
  87580. uronic
  87581. containing
  87582. polysac
  87583. schweizer
  87584. meeder
  87585. benzopyrans
  87586. tamelen
  87587. accounts
  87588. total
  87589. synthesis
  87590. fujita
  87591. synthesis
  87592. gibberellins
  87593. dioxaborinanyl
  87594. allyl
  87595. diisopinocampheylbor
  87596. excepti
  87597. grovenstein
  87598. migrations
  87599. organometallic
  87600. compounds
  87601. havinga
  87602. cornelisse
  87603. hecker
  87604. toxic
  87605. irritant
  87606. cocarcinogenic
  87607. diterpene
  87608. hecker
  87609. toxic
  87610. irritant
  87611. cocarcinogenic
  87612. diterpene
  87613. levkoeva
  87614. yakhontov
  87615. synthesis
  87616. heterocyclic
  87617. negishi
  87618. idacavage
  87619. reactions
  87620. format
  87621. negishi
  87622. takahashi
  87623. aldrichimica
  87624. negishi
  87625. organometal
  87626. chemistry
  87627. corey
  87628. greene
  87629. miller
  87630. euranto
  87631. mechanisms
  87632. catalysis
  87633. vinyl
  87634. ester
  87635. hydrolys
  87636. kuhle
  87637. klauke
  87638. fluorinated
  87639. isocyanates
  87640. derivatives
  87641. organic
  87642. chemistry
  87643. superoxide
  87644. chemica
  87645. leete
  87646. porwoll
  87647. aldrichimica
  87648. lukevics
  87649. hydrosilylation
  87650. reaction
  87651. russian
  87652. cherkasova
  87653. bogatkov
  87654. golovina
  87655. tertiary
  87656. amines
  87657. kaiser
  87658. petty
  87659. knutson
  87660. polyalkalimetal
  87661. deriv
  87662. negishi
  87663. takahashi
  87664. aldrichimica
  87665. organo
  87666. walker
  87667. functional
  87668. group
  87669. stanoeva
  87670. khaimova
  87671. heterocycl
  87672. compds
  87673. brown
  87674. addition
  87675. hydrogen
  87676. cyanide
  87677. olefins
  87678. organi
  87679. krongauz
  87680. alpha
  87681. diketones
  87682. related
  87683. polyme
  87684. schacht
  87685. hypolipidemic
  87686. aryloxyacetic
  87687. acids
  87688. topic
  87689. schmitz
  87690. electrophilic
  87691. amination
  87692. steckhan
  87693. angew
  87694. indirect
  87695. elect
  87696. kaiser
  87697. reactions
  87698. sulfonate
  87699. sulfate
  87700. esters
  87701. organic
  87702. brown
  87703. synthesis
  87704. willgerodt
  87705. reaction
  87706. revie
  87707. dehmlow
  87708. advances
  87709. phase
  87710. transfer
  87711. catalysis
  87712. vedejs
  87713. ylides
  87714. vilsmaier
  87715. diacylmethylene
  87716. wasserman
  87717. hutton
  87718. triplet
  87719. states
  87720. cyclic
  87721. wenkert
  87722. buckwalter
  87723. burfitt
  87724. gasic
  87725. gottlieb
  87726. winterfeldt
  87727. synthesis
  87728. applications
  87729. diisobutyla
  87730. e-cyanide
  87731. e-unsaturated
  87732. e-viniferin
  87733. eactants
  87734. eactions
  87735. ealick
  87736. earlp
  87737. early
  87738. early
  87739. birds
  87740. chiral
  87741. boranes
  87742. earthz
  87743. easily
  87744. eastern
  87745. easton
  87746. easton
  87747. christopher
  87748. carbon
  87749. centered
  87750. radicals
  87751. amino
  87752. eastwood
  87753. access
  87754. highly
  87755. functionalized
  87756. bicyclic
  87757. lactones
  87758. eaton
  87759. eaton
  87760. towards
  87761. dodecahedrane
  87762. tetrahedron
  87763. ebelacatone
  87764. eberhardt
  87765. eberson
  87766. eberson
  87767. lennart
  87768. outer
  87769. sphereelectrontransf
  87770. reactions
  87771. ebetino
  87772. ebmeyer
  87773. ebmeyer
  87774. vogtle
  87775. small
  87776. large
  87777. molec
  87778. ebrey
  87779. eburnamine
  87780. eburnane
  87781. ecbegoyen
  87782. eceptors
  87783. echegoyen
  87784. echeverria
  87785. echinoderm
  87786. echinoderms
  87787. echner
  87788. eckstein
  87789. eckstein
  87790. phosphorothioate
  87791. analogues
  87792. nucleotides
  87793. eckstein
  87794. fritz
  87795. oligonucleotides
  87796. analogs
  87797. practical
  87798. eckstein
  87799. urbanski
  87800. 0xazine
  87801. derivatives
  87802. advan
  87803. ecology
  87804. economic
  87805. economical
  87806. economy
  87807. ective
  87808. ectron
  87809. ecular
  87810. ecules
  87811. edgar
  87812. edith
  87813. editionQ
  87814. edition
  87815. editor
  87816. editors
  87817. edlund
  87818. edlund
  87819. buncel
  87820. erwin
  87821. electronic
  87822. configuration
  87823. structure
  87824. edman
  87825. edmonds
  87826. edmonds
  87827. francesconi
  87828. stick
  87829. arsenic
  87830. compounds
  87831. edmund
  87832. edmundo
  87833. edmunds
  87834. edstrom
  87835. education
  87836. edulis
  87837. edward
  87838. edwards
  87839. edwin
  87840. effect
  87841. trile
  87842. anions
  87843. versus
  87844. effect
  87845. alkene
  87846. substituents
  87847. molybdenum
  87848. chromium
  87849. effect
  87850. alteration
  87851. heterocyclic
  87852. nucleus
  87853. effect
  87854. chiral
  87855. quaternary
  87856. ammonium
  87857. salts
  87858. salen
  87859. manganes
  87860. effect
  87861. chiral
  87862. quaternary
  87863. ammonium
  87864. salts
  87865. salen
  87866. catal
  87867. effect
  87868. chiral
  87869. quaternary
  87870. ammonium
  87871. salts
  87872. salen
  87873. mn-catal
  87874. effect
  87875. conformational
  87876. change
  87877. reactivit
  87878. organic
  87879. effect
  87880. coordinating
  87881. ligands
  87882. pauson
  87883. khand
  87884. cycloaddi
  87885. effect
  87886. electron
  87887. donor
  87888. reactivity
  87889. lithi
  87890. effect
  87891. oi-pr
  87892. stereoselectivity
  87893. halocyclization
  87894. effected
  87895. effecting
  87896. effective
  87897. effective
  87898. effective
  87899. molarities
  87900. intramolecular
  87901. reactions
  87902. effectivity
  87903. effectors
  87904. effects
  87905. effects
  87906. methyl
  87907. group
  87908. substitution
  87909. effects
  87910. silicon
  87911. atoms
  87912. energies
  87913. effects
  87914. strong
  87915. electron
  87916. withdrawing
  87917. bortylsubstituent
  87918. effects
  87919. butyl
  87920. group
  87921. substitution
  87922. reactivity
  87923. effects
  87924. changes
  87925. ligands
  87926. skeleton
  87927. effects
  87928. substituents
  87929. medium
  87930. acidity
  87931. effenberger
  87932. effenberger
  87933. electrophilic
  87934. reagents
  87935. recent
  87936. developments
  87937. effenberger
  87938. synthesis
  87939. reactions
  87940. optically
  87941. active
  87942. effenberger
  87943. franz
  87944. christoph
  87945. terminally
  87946. substituted
  87947. effic
  87948. efficiencies
  87949. efficiency
  87950. efficient
  87951. efficient
  87952. efficient
  87953. coupling
  87954. dimethyl
  87955. amino
  87956. using
  87957. efficient
  87958. nitrogen
  87959. expansion
  87960. process
  87961. facilitated
  87962. efficient
  87963. opening
  87964. trans
  87965. epoxybutane
  87966. higher
  87967. order
  87968. efficient
  87969. reaction
  87970. channels
  87971. monocharides
  87972. disacchari
  87973. efficient
  87974. reductive
  87975. etherification
  87976. carbonyl
  87977. compounds
  87978. efficient
  87979. rhodium
  87980. catalyzed
  87981. hydrogenation
  87982. aldehydes
  87983. efficient
  87984. stereoselective
  87985. access
  87986. polyhydroxylated
  87987. indoliz
  87988. efficient
  87989. synthesis
  87990. aminothioacrylamides
  87991. iminoformyl
  87992. efficient
  87993. synthesis
  87994. substituted
  87995. indoles
  87996. palladium
  87997. efficient
  87998. synthesis
  87999. heteroradialenes
  88000. reaction
  88001. efficient
  88002. synthesis
  88003. quinodimethanes
  88004. prepare
  88005. efficient
  88006. total
  88007. synthesis
  88008. pharmacophore
  88009. antica
  88010. effieient
  88011. efraty
  88012. efremovM
  88013. egbert
  88014. egenburg
  88015. egenburg
  88016. methods
  88017. synthesis
  88018. properties
  88019. egorochkin
  88020. egorochkin
  88021. conjunction
  88022. organic
  88023. compounds
  88024. silic
  88025. egorov
  88026. eguchi
  88027. eguchi
  88028. shoji
  88029. matsushita
  88030. yamashita
  88031. keizo
  88032. wittig
  88033. ehninger
  88034. reaction
  88035. sulphilimines
  88036. related
  88037. compounds
  88038. eicher
  88039. eichhorn
  88040. eicosanoid
  88041. eicosanoids
  88042. eiduss
  88043. eigenvectors
  88044. eight
  88045. eight
  88046. -membered
  88047. eight-membered
  88048. rings
  88049. eighteenth
  88050. eiichi
  88051. eiimination
  88052. toshio
  88053. tagaki
  88054. waichiro
  88055. metal
  88056. effects
  88057. reactio
  88058. einhorn
  88059. eisch
  88060. eisenberg
  88061. eisenberg
  88062. atmospheric
  88063. phase
  88064. generation
  88065. singlet
  88066. eistert
  88067. either
  88068. ekkehard
  88069. eklund
  88070. eksterowicz
  88071. eksterowicz
  88072. transition
  88073. state
  88074. modeling
  88075. ashry
  88076. rashed
  88077. ramadan
  88078. condensed
  88079. triaz
  88080. el'kinsonm
  88081. el'tsov
  88082. elaal
  88083. elaboration
  88084. elaborations
  88085. elander
  88086. elationship
  88087. eleanora
  88088. elecrophilic
  88089. electrical
  88090. electro
  88091. electro-organic
  88092. electro-organic
  88093. synthesis
  88094. electrocatalytic
  88095. electrocatalytic
  88096. hydrogenation
  88097. hydrogen-active
  88098. electrodes
  88099. electrochemicall
  88100. electrochemical
  88101. activation
  88102. sulfur
  88103. organic
  88104. solvents
  88105. electrochemical
  88106. methods
  88107. generation
  88108. carbenes
  88109. electrochemical
  88110. preparation
  88111. amidoalkylation
  88112. reage
  88113. electrochemical
  88114. reactions
  88115. fluoroorganic
  88116. compounds
  88117. electrochemical
  88118. reactions
  88119. organosilicon
  88120. compounds
  88121. electrochemical
  88122. reductions
  88123. electrochemical
  88124. synthesis
  88125. pyridines
  88126. electrochemically
  88127. electrochemiiuminesc
  88128. electrochemistry
  88129. electrochemistry
  88130. organic
  88131. synthesis
  88132. electrochemistry
  88133. organic
  88134. synthesis
  88135. review
  88136. electrocyclic
  88137. electrocyclic
  88138. electrocyclic
  88139. opening
  88140. reactions
  88141. ethylene
  88142. oxides
  88143. electrocyclization
  88144. electrocyclizations
  88145. electrode
  88146. electrodes
  88147. electroenzymatick
  88148. electroenzymatic
  88149. synthesis
  88150. electrogenerated
  88151. electrolysis
  88152. electrolysis
  88153. n-heterocyclic
  88154. compounds
  88155. electrolytes
  88156. electrolytic
  88157. electrolytic
  88158. reductive
  88159. coupling
  88160. electrolytic
  88161. reductive
  88162. coupling
  88163. synthetic
  88164. mechanistic
  88165. electrolytically
  88166. electronq
  88167. electron
  88168. electron
  88169. deficient
  88170. boron
  88171. carbon
  88172. clusters
  88173. electron
  88174. deficient
  88175. carbocations
  88176. review
  88177. electron
  88178. transfer
  88179. thermal
  88180. photochemical
  88181. activatio
  88182. electron
  88183. transfer
  88184. induced
  88185. intramolecular
  88186. cycloaddition
  88187. electron
  88188. transfer
  88189. reaction
  88190. organic
  88191. chemistry
  88192. electron
  88193. transfer
  88194. reactions
  88195. followed
  88196. rapid
  88197. cleavage
  88198. electron
  88199. transfer
  88200. reactions
  88201. organic
  88202. chemistry
  88203. electron-deficient
  88204. electron-deficient
  88205. carbocations
  88206. electron-exchange
  88207. electron-rich
  88208. electron-spin-echo
  88209. electron-transfer
  88210. electron-transfer
  88211. initiated
  88212. reactions
  88213. electron-transfer
  88214. mechanisms
  88215. organometallic
  88216. intermediate
  88217. electron-transfer
  88218. oxidation
  88219. electron-transfer
  88220. processes
  88221. peroxydisulfate
  88222. useful
  88223. electron-transfer-in
  88224. electron-withdrawing
  88225. electronegatively
  88226. electronegatively
  88227. substituted
  88228. carbocations
  88229. electronicO
  88230. electronic
  88231. electronic
  88232. amplification
  88233. selectivity
  88234. rhodium
  88235. catalyzed
  88236. electronic
  88237. steric
  88238. control
  88239. insertion
  88240. reactions
  88241. electronic
  88242. aspects
  88243. organic
  88244. photochemistry
  88245. electronic
  88246. effects
  88247. dirhodium
  88248. carboxylates
  88249. linear
  88250. electronic
  88251. effects
  88252. stereochemical
  88253. outcome
  88254. electronic
  88255. substituent
  88256. effects
  88257. catalyzed
  88258. electronically
  88259. electronically
  88260. neutral
  88261. 2-aza-13-dienes
  88262. useful
  88263. inter
  88264. electronics
  88265. electronicspectra
  88266. electrons
  88267. electroorganic
  88268. electroorganic
  88269. chemistry
  88270. electroreductive
  88271. coupling
  88272. electroorganic
  88273. chemistry
  88274. organic
  88275. synthesis
  88276. electroorganic
  88277. syntheses
  88278. nitrogen
  88279. heterocycles
  88280. electroorganic
  88281. synthesis
  88282. electrooxidation
  88283. electrophile
  88284. electrophile
  88285. induced
  88286. cyclization
  88287. d-alkenylimines
  88288. electrophiles
  88289. electrophili
  88290. electrophilic
  88291. electrophilic
  88292. addition
  88293. reagents
  88294. alkenes
  88295. alkyne
  88296. electrophilic
  88297. amination
  88298. carbanions
  88299. electrophilic
  88300. amination
  88301. carbanions
  88302. metallated
  88303. electrophilic
  88304. amination
  88305. higher
  88306. order
  88307. cuprates
  88308. electrophilic
  88309. aminations
  88310. oxaziridines
  88311. electrophilic
  88312. aromatic
  88313. substitution
  88314. electrophilic
  88315. bromination
  88316. carbon-carbon
  88317. double
  88318. bonds
  88319. electrophilic
  88320. c-nitroso
  88321. compounds
  88322. electrophilic
  88323. cyclopropanes
  88324. organic
  88325. synthesis
  88326. electrophilic
  88327. diazoalkane
  88328. substitution
  88329. electrophilic
  88330. heteroatom
  88331. cyclizations
  88332. electrophilic
  88333. metal
  88334. carbenes
  88335. reaction
  88336. intermediates
  88337. electrophilic
  88338. substitution
  88339. heterocycles
  88340. quantitative
  88341. electrophilic
  88342. substitution
  88343. organomercurials
  88344. electrophilic
  88345. substitution
  88346. organosilicon
  88347. compounds-applic
  88348. electrophilicity
  88349. electrophitic
  88350. electrophoresis
  88351. electroplilic
  88352. electropositive
  88353. electroreduced
  88354. electroreduction
  88355. electroreductive
  88356. electroreductive
  88357. intramolecular
  88358. coupling
  88359. nonconjugated
  88360. electrosorption
  88361. electrospray
  88362. electrostatic
  88363. electrosynthesis
  88364. elemane
  88365. element
  88366. element
  88367. elemental
  88368. fluorine
  88369. legitimate
  88370. reagent
  88371. lective
  88372. elemental
  88373. phosphorus-strong
  88374. system
  88375. synthes
  88376. elements
  88377. elena
  88378. eleonora
  88379. eletons
  88380. eleven
  88381. eleventh
  88382. elezbawy
  88383. elfahham
  88384. elferink
  88385. elferink
  88386. breitgoff
  88387. kloosterman
  88388. kamphuis
  88389. elferink
  88390. breitgoff
  88391. kloostermnn
  88392. kamphuis
  88393. elgemeie
  88394. elgemeie
  88395. elezbawy
  88396. mansour
  88397. synthesis
  88398. elgemie
  88399. elguero
  88400. elguero
  88401. claramunt
  88402. summers
  88403. chemistry
  88404. aroma
  88405. elias
  88406. elicited
  88407. elicitor-active
  88408. eliel
  88409. eliel
  88410. eliel
  88411. pietrusiewicz
  88412. nonaromatic
  88413. heterocyc
  88414. eliel
  88415. ernest
  88416. cologne
  88417. chapel
  88418. proflles
  88419. pathways
  88420. eliel
  88421. ernest
  88422. wilen
  88423. samuel
  88424. mander
  88425. lewis
  88426. stereochemistry
  88427. elimination
  88428. elimination-addition
  88429. elimination-reaction
  88430. eliminations
  88431. eliminations
  88432. alkenes
  88433. allenes
  88434. alkynes
  88435. related
  88436. eliminative
  88437. elisa
  88438. elisas
  88439. elizabeth
  88440. ellagitannin
  88441. ellen
  88442. ellenberger
  88443. eller
  88444. eller
  88445. karsten
  88446. schwarz
  88447. helmut
  88448. organometallic
  88449. chemistry
  88450. ellerd
  88451. ellington
  88452. elliott
  88453. elliott
  88454. janes
  88455. synthetic
  88456. pyrethroids
  88457. class
  88458. elliott
  88459. progress
  88460. design
  88461. insecticides
  88462. elliptic
  88463. ellipticine
  88464. ellipticines
  88465. ellis
  88466. elmoghayar
  88467. elmoghayer
  88468. elmore
  88469. elmsford
  88470. elnagdi
  88471. elnagdi
  88472. mohamed
  88473. hilmy
  88474. abdalla
  88475. mohamed
  88476. sadek
  88477. kamal
  88478. elongation/annulatio
  88479. elopments
  88480. elschenbroich
  88481. elschenbroich
  88482. christoph
  88483. salzer
  88484. albrecht
  88485. organo
  88486. metallics
  88487. elsevierV
  88488. elliott
  88489. progress
  88490. design
  88491. insecticides
  88492. elsevier
  88493. emitting@
  88494. employing
  88495. enamine@
  88496. enantio
  88497. diastereo
  88498. regioselective
  88499. zirconium
  88500. catalyzed
  88501. enantiomerically
  88502. compound
  88503. syntheses
  88504. forma@
  88505. enantiopure
  88506. building
  88507. blocks
  88508. sugars
  88509. their
  88510. utilizatio@
  88511. enantioselective
  88512. enantioselective
  88513. wittig
  88514. rearrangement
  88515. involving
  88516. chiral
  88517. enantioselective
  88518. addition
  88519. organozinc
  88520. reagents
  88521. aldehyde@
  88522. enantioselective
  88523. catalytic
  88524. hydrogenation@
  88525. enantioselective
  88526. radical
  88527. carbon-carbon
  88528. forming
  88529. enantioselective
  88530. hydrogenation
  88531. b-substituted
  88532. a-acetamidoa@
  88533. enantioselective
  88534. reduction
  88535. ketones
  88536. sodium
  88537. borohydrid@
  88538. enantioselective
  88539. synthesis
  88540. advanced
  88541. intermediate
  88542. enantioselective
  88543. synthesis
  88544. indolizidine
  88545. alkaloids
  88546. boro@
  88547. enantioselective
  88548. synthesis
  88549. using
  88550. crude
  88551. enzymes@
  88552. lbert
  88553. leowenthal
  88554. chemistry
  88555. potentially
  88556. elsevier
  88557. elsewhere
  88558. elucidated
  88559. elucidation
  88560. elusive
  88561. elvain
  88562. elvidge
  88563. elzbieta
  88564. emanuel
  88565. emanuel
  88566. zaikov
  88567. maizus
  88568. oxidation
  88569. organic
  88570. compo
  88571. emanuela
  88572. emel'yanov
  88573. emergence
  88574. emergence
  88575. cyano
  88576. complex
  88577. based
  88578. organometallic
  88579. emerging
  88580. emerson
  88581. emile
  88582. emilio
  88583. eminent
  88584. emission
  88585. emistry
  88586. emmons
  88587. emphasis
  88588. empirical
  88589. employed
  88590. employing
  88591. employing
  88592. emrani
  88593. emsley
  88594. emulation
  88595. lization
  88596. phosphoryl
  88597. group
  88598. enallenic
  88599. enals
  88600. nones
  88601. enamide
  88602. enamides
  88603. enamine
  88604. precursors
  88605. 1-substituted-1234-t
  88606. peter
  88607. enamine
  88608. rearrangement
  88609. enamines
  88610. enamines
  88611. formamides
  88612. synthesis
  88613. tetrahydro
  88614. enamines
  88615. recent
  88616. advances
  88617. synthetic
  88618. spectroscopic
  88619. mechanis
  88620. enamines
  88621. synthesis
  88622. structure
  88623. reactions
  88624. enamino
  88625. enaminones
  88626. enaminonitriles
  88627. enantio
  88628. enantio
  88629. diastereoselectivity
  88630. intramolecular
  88631. cyclo
  88632. enantio
  88633. diastereo
  88634. regioselective
  88635. zirconium
  88636. catalyzed
  88637. enantioconrolled
  88638. enantiocontrol
  88639. enantiocontrolled
  88640. enantiodifferentiati
  88641. enantiodifferentiati
  88642. transformation
  88643. prochiral
  88644. polyols
  88645. enantioenriched
  88646. enantioface
  88647. enantiomer
  88648. enantiomeric
  88649. enantiomerically
  88650. merically
  88651. cyclopentadienes
  88652. enantiomers
  88653. enantiomers
  88654. racemates
  88655. resolutions
  88656. enantionmeric
  88657. enantioposition-sele
  88658. enantiopure
  88659. enantiopure
  88660. building
  88661. blocks
  88662. sugars
  88663. their
  88664. utilizatio
  88665. enantiopure
  88666. thiosulfonium
  88667. salts
  88668. asymmetric
  88669. synthesis
  88670. enantiopurecarbohydr
  88671. enantiosele
  88672. enantiosele
  88673. synthesis
  88674. natural
  88675. products
  88676. chiral
  88677. enantioselection
  88678. enantioselectivet
  88679. enantioselective
  88680. diethylzinc
  88681. aldehydes
  88682. cataly
  88683. enantioselective
  88684. addition
  88685. diethylzinc
  88686. aldehydes
  88687. using
  88688. enantioselective
  88689. addition
  88690. organometallic
  88691. reagents
  88692. enantioselective
  88693. addition
  88694. organozinc
  88695. reagents
  88696. aldehyde
  88697. enantioselective
  88698. addition
  88699. reaction
  88700. trimethylsilyl
  88701. cyanide
  88702. enantioselective
  88703. aerobic
  88704. epoxidation
  88705. acyclic
  88706. simple
  88707. olefi
  88708. enantioselective
  88709. aminohydroxylation
  88710. alkenes
  88711. enantioselective
  88712. diastereoselective
  88713. catalysis
  88714. enantioselective
  88715. diastereoselective
  88716. molecular
  88717. recognitio
  88718. enantioselective
  88719. catalysis
  88720. chiral
  88721. cobalt
  88722. copper
  88723. enantioselective
  88724. catalysis
  88725. metal
  88726. complexes
  88727. enantioselective
  88728. catalysis
  88729. transition
  88730. metal
  88731. complexes
  88732. enantioselective
  88733. construction
  88734. spiro
  88735. cyclopropane
  88736. bicyc
  88737. enantioselective
  88738. deprotonation
  88739. vehicle
  88740. asymmetr
  88741. enantioselective
  88742. epoxidation
  88743. chromene
  88744. derivatives
  88745. using
  88746. enantioselective
  88747. epoxidation
  88748. unfunctionalized
  88749. alkenes
  88750. enantioselective
  88751. epoxidation
  88752. peroxidic
  88753. oxygen
  88754. enantioselective
  88755. formation
  88756. bicyclic
  88757. lactones
  88758. rhodium
  88759. enantioselective
  88760. hydrogenation
  88761. b-substituted
  88762. a-acetamidoa
  88763. enantioselective
  88764. intramolecular
  88765. insertion
  88766. reaction
  88767. enantioselective
  88768. intramolecular
  88769. insertion
  88770. reactions
  88771. enantioselective
  88772. intramolecular
  88773. cyclopropanation
  88774. allyli
  88775. enantioselective
  88776. intramolecular
  88777. cyclopropanations
  88778. allylic
  88779. enantioselective
  88780. methods
  88781. chiral
  88782. cyclohexane
  88783. synthes
  88784. enantioselective
  88785. nickel
  88786. catalyzed
  88787. grignard
  88788. cross
  88789. coupling
  88790. enantioselective
  88791. nitration
  88792. chiral
  88793. crotylsilanes
  88794. conci
  88795. enantioselective
  88796. oxidation
  88797. chiral
  88798. titanium
  88799. enolates
  88800. deriv
  88801. enantioselective
  88802. oxidation
  88803. secondary
  88804. alcohols
  88805. using
  88806. enantioselective
  88807. preparation
  88808. cyclohexadiene
  88809. enantioselective
  88810. protonation
  88811. enolates
  88812. using
  88813. chiral
  88814. acids
  88815. enantioselective
  88816. synthesis
  88817. 12-disubstituted
  88818. mitosene
  88819. enantioselective
  88820. synthesis
  88821. bicyclo
  88822. 3.1.0
  88823. hexane
  88824. a-ring
  88825. enantioselective
  88826. synthesis
  88827. amino
  88828. acids
  88829. enantioselective
  88830. synthesis
  88831. advanced
  88832. intermediate
  88833. enantioselective
  88834. synthesis
  88835. diastereomers
  88836. including
  88837. enantioselective
  88838. synthesis
  88839. carbapenem
  88840. antibiotics
  88841. enantioselective
  88842. synthesis
  88843. carbohydrate
  88844. precursors
  88845. enantioselective
  88846. synthesis
  88847. diverse
  88848. a-amino
  88849. phosphonate
  88850. enantioselective
  88851. synthesis
  88852. indolizidine
  88853. alkaloids
  88854. formal
  88855. enantioselective
  88856. synthesis
  88857. nagilactone
  88858. vinylsilane
  88859. enantioselective
  88860. synthesis
  88861. natural
  88862. austalide
  88863. unusual
  88864. enantioselective
  88865. synthesis
  88866. non-racemic
  88867. chiral
  88868. molecules
  88869. enantioselective
  88870. synthesis
  88871. nonproteinogenic
  88872. amino
  88873. acids
  88874. enantioselective
  88875. synthesis
  88876. organic
  88877. compounds
  88878. optical
  88879. enantioselective
  88880. synthesis
  88881. organic
  88882. compounds
  88883. optival
  88884. enantioselective
  88885. synthesis
  88886. tertiary
  88887. homoallylic
  88888. alcohols
  88889. enantioselective
  88890. synthesis
  88891. using
  88892. chira
  88893. heterogeneous
  88894. catalys
  88895. enantioselective
  88896. synthesis
  88897. using
  88898. crude
  88899. enzymes
  88900. enantioselective
  88901. synthesis
  88902. optically
  88903. active
  88904. transition
  88905. enantioselective
  88906. total
  88907. synthesis
  88908. 7-deacetoxyalcyonin
  88909. total
  88910. synthesis
  88911. chlorothricolide
  88912. enantioselective
  88913. total
  88914. synthesis
  88915. gracilins
  88916. using
  88917. enantioselective
  88918. total
  88919. synthesis
  88920. isolaurepinnacin
  88921. enantioselective
  88922. total
  88923. synthesis
  88924. miroestrol
  88925. enantioselective
  88926. total
  88927. synthesis
  88928. oleanolic
  88929. erythrodi
  88930. enantioselective
  88931. total
  88932. synthesis
  88933. strychnine
  88934. enantioselective
  88935. total
  88936. synthesis
  88937. subergorgic
  88938. enantioselective
  88939. transformations
  88940. racemization
  88941. studies
  88942. enantioselective
  88943. transition
  88944. metal-catalyzed
  88945. hydrogenation
  88946. enantioselectives
  88947. enantioselectivity
  88948. enantioselectivity
  88949. lipases
  88950. control
  88951. prediction
  88952. enantioseparation
  88953. enantioseparation
  88954. enantiospecific
  88955. enantiospecific
  88956. synthesis
  88957. transformations
  88958. chiral
  88959. pool-
  88960. enantiospecific
  88961. synthesis
  88962. amino
  88963. methyl
  88964. phosphonobut
  88965. enantiospecific
  88966. synthesis
  88967. diastereomers
  88968. 2-met
  88969. enantiospecific
  88970. total
  88971. synthesis
  88972. protein
  88973. phosphatase
  88974. enantiospecificity
  88975. enchanting
  88976. encina
  88977. encinas
  88978. encoding
  88979. ender
  88980. enders
  88981. endiandric
  88982. ending
  88983. phenyl
  88984. azabicyclo
  88985. 2.2.1
  88986. heptane
  88987. pressure
  88988. hasumi
  88989. reductase
  88990. inhibitors
  88991. natural
  88992. product
  88993. endo-selective
  88994. endo-selective
  88995. cyclization
  88996. pathways
  88997. intramolecular
  88998. endo-stereoselective
  88999. endo/exo
  89000. endo/exo
  89001. selectivity
  89002. cycloadditions
  89003. dihydropyridine
  89004. endocyclic
  89005. endogenous
  89006. endogenous
  89007. endoperoxides
  89008. endor
  89009. endotoxin
  89010. approach
  89011. asymmetric
  89012. catalysis
  89013. sakurai
  89014. hosomi
  89015. reaction
  89016. method
  89017. functionalization
  89018. fuller
  89019. reactions
  89020. phosphaalkene
  89021. enophile
  89022. reactions
  89023. alkenes
  89024. enophiles
  89025. ene-12-di-x
  89026. ene-12-di-x
  89027. compounds
  89028. ene-diyne
  89029. ene-halogen
  89030. ene-halogen
  89031. compounds
  89032. ene-n
  89033. ene-n
  89034. ompounds
  89035. ene-o-compounds
  89036. ene-s
  89037. ene-s
  89038. compounds
  89039. ene-type
  89040. enecarbamates
  89041. enediol
  89042. enediyne
  89043. enediynes
  89044. enehydroxylamines
  89045. enehydroxylamines
  89046. versatile
  89047. compounds
  89048. sigmatropic
  89049. enenitrile
  89050. energetic
  89051. energetics
  89052. energies
  89053. energy
  89054. enethiolates
  89055. eneyne
  89056. eneynes
  89057. enforced
  89058. engbersen
  89059. engberts
  89060. engberts
  89061. catalysis
  89062. surfactant
  89063. aggregates
  89064. engdahl
  89065. engel
  89066. engel
  89067. engel
  89068. michael
  89069. projection
  89070. fischer
  89071. engel
  89072. mechanisms
  89073. thermal
  89074. photochemical
  89075. decomp
  89076. engel
  89077. robert
  89078. handbook
  89079. organophosphorus
  89080. chemistry
  89081. dekker
  89082. engelhardt
  89083. engelhardt
  89084. translated
  89085. german
  89086. nikov
  89087. engelking
  89088. engelking
  89089. spectroscopy
  89090. cooled
  89091. radical
  89092. engels
  89093. engen
  89094. engendered
  89095. engewald
  89096. engewald
  89097. reinhardt
  89098. steinborn
  89099. shape
  89100. selectiv
  89101. engineered
  89102. engineering
  89103. england
  89104. englert
  89105. englert
  89106. gerhard
  89107. carotenoids
  89108. novel
  89109. experimental
  89110. techni
  89111. englewood
  89112. engligh
  89113. englisch
  89114. englisch
  89115. gauss
  89116. dieter
  89117. chemically
  89118. modified
  89119. oligonucleot
  89120. english
  89121. english
  89122. engman
  89123. enhanced
  89124. enhancement
  89125. enhancing
  89126. enhancing
  89127. yield
  89128. diastereoselectivity
  89129. pictet
  89130. enikolpyan
  89131. enium
  89132. enjoying
  89133. enkephalin
  89134. enlargement
  89135. ennan
  89136. enoate
  89137. enoates
  89138. enoic
  89139. enoids
  89140. thioethers
  89141. substitutes
  89142. their
  89143. alkylat
  89144. triflate
  89145. pyranoses
  89146. versatile
  89147. reagents
  89148. formation
  89149. enol-keto
  89150. enolate
  89151. enolate
  89152. other
  89153. carbon
  89154. nucleophile
  89155. alkylation
  89156. reactions
  89157. enolate-imine
  89158. enolates
  89159. enolboration
  89160. enolboration
  89161. dicyclohexyliodobora
  89162. versitile
  89163. reagent
  89164. enolisation
  89165. enolisation
  89166. simple
  89167. carbonyl
  89168. compounds
  89169. related
  89170. reactio
  89171. enolizable
  89172. enolization
  89173. enols
  89174. other
  89175. reactive
  89176. species
  89177. enolsilanes
  89178. enoltriflates
  89179. enone
  89180. enone
  89181. dienone
  89182. rearrangements
  89183. enone
  89184. cycloadditions
  89185. rearrangements
  89186. photoreactions
  89187. enone
  89188. olefins
  89189. photochemical
  89190. cycloadditions
  89191. enone
  89192. photoannulation
  89193. enone-olefin
  89194. enones
  89195. enophile
  89196. enophiles
  89197. enoxysilacyclobutane
  89198. enprostil
  89199. enriched
  89200. enriched
  89201. entropy
  89202. entryD
  89203. entwhistle
  89204. enumerating
  89205. enumeration
  89206. environment
  89207. environmental
  89208. environmental
  89209. proper
  89210. polymers
  89211. starting
  89212. materials
  89213. environmentally
  89214. environments
  89215. enylamines
  89216. enylidenes
  89217. enylphosphonates
  89218. enyne
  89219. enynes
  89220. enzell
  89221. enzell
  89222. wahlberg
  89223. aasen
  89224. isoprenoids
  89225. alkaloids
  89226. enzymatic
  89227. enzymatic
  89228. lization
  89229. squalene
  89230. oxidosqualene
  89231. stero
  89232. enzymatic
  89233. methods
  89234. preparative
  89235. carbohydrate-chemist
  89236. enzyme
  89237. enzyme
  89238. catalysis
  89239. synthetic
  89240. carbohydrate
  89241. chemistry
  89242. enzyme
  89243. catalyzed
  89244. organic
  89245. synthesis
  89246. practical
  89247. routes
  89248. enzyme
  89249. mimics
  89250. enzyme
  89251. model
  89252. organometalli
  89253. chemistry
  89254. enzyme
  89255. modelling
  89256. crown
  89257. ethers
  89258. enzyme
  89259. models
  89260. based
  89261. cyclodextrin
  89262. enzyme
  89263. reactivity
  89264. organic
  89265. perspective
  89266. enzyme-catalysed
  89267. enzyme-catalysed
  89268. synthesis
  89269. carbohydrates
  89270. enzyme-catalyzed
  89271. enzyme-catalyzed
  89272. allylic
  89273. rearrangements
  89274. enzyme-catalyzed
  89275. irreversible
  89276. transfer
  89277. enzyme-catalyzed
  89278. organic
  89279. synthesis
  89280. practical
  89281. routes
  89282. enzyme-inhibitors
  89283. enzyme-mediated
  89284. enzymes
  89285. enzymes
  89286. enzymes
  89287. chiral
  89288. catalysts
  89289. enzymes
  89290. carbohydrate
  89291. peptide
  89292. syntheses
  89293. enzymes
  89294. asymmetric
  89295. synthesis
  89296. enzymes
  89297. organic
  89298. synthesis
  89299. enzymes
  89300. organic
  89301. synthesis
  89302. alteration
  89303. reversible
  89304. reacti
  89305. enzymes
  89306. organic-synthesis
  89307. alteration
  89308. reversible-reacti
  89309. enzymes
  89310. synthetic
  89311. organic
  89312. chemistry
  89313. enzymic
  89314. enzymic
  89315. hydroxylation
  89316. arene
  89317. symmetry
  89318. considerations
  89319. enzymic
  89320. methods
  89321. preparative
  89322. carbohydrate
  89323. chemistry
  89324. enzymic
  89325. methods
  89326. resolving
  89327. racemates
  89328. amino
  89329. acids
  89330. enzymic
  89331. protecting
  89332. group
  89333. techniques
  89334. enzymic
  89335. reaction
  89336. selectivity
  89337. negative
  89338. catalysis
  89339. enzymology
  89340. eparation
  89341. ephedrines
  89342. ephritikhine
  89343. ephritikhine
  89344. michel
  89345. recent
  89346. advances
  89347. organochemistry
  89348. epibatidine
  89349. epilupinine
  89350. epimer
  89351. epimerization
  89352. epimerization
  89353. glycopyranosides
  89354. during
  89355. cyclization
  89356. epinupharamine
  89357. epiotis
  89358. epiotis
  89359. theory
  89360. organic
  89361. reactions
  89362. springer
  89363. verlag
  89364. epiotis
  89365. shaik
  89366. zander
  89367. rearrangements
  89368. theoretical
  89369. episelenonium
  89370. episulfide
  89371. episulfides
  89372. episulfone
  89373. episulfonium
  89374. episulfonium
  89375. episelenonium
  89376. versatile
  89377. heterocyc
  89378. episulphones
  89379. epoxidationG
  89380. epoxidation
  89381. hydroxylation
  89382. ethylenic
  89383. compounds
  89384. epoxidation
  89385. related
  89386. processes
  89387. epoxidations
  89388. epoxide
  89389. epoxide
  89390. resins
  89391. epoxidess
  89392. epoxyE
  89393. epoxyalkenes
  89394. epoxyalkyl
  89395. epoxybutane
  89396. epoxycyclodeca
  89397. epoxydictymene
  89398. epoxyesters
  89399. epoxyisoindolines
  89400. epoxypropyl
  89401. epoxysilanes
  89402. epoxysulfoxides
  89403. epstein
  89404. epsztajn
  89405. epsztein
  89406. eptazocine
  89407. equation
  89408. equations
  89409. equilibrating
  89410. equilibration
  89411. equilibria
  89412. equilibrium
  89413. equimolar
  89414. equivalent
  89415. valents
  89416. erastov
  89417. erdik
  89418. eremeev
  89419. eremenko
  89420. eremophilane
  89421. erfanian
  89422. erfluoroalkylation
  89423. erful
  89424. ergoline
  89425. ergostane
  89426. ergot
  89427. erian
  89428. erian
  89429. ayman
  89430. wahba
  89431. chemistry
  89432. enaminonitriles
  89433. erich
  89434. erickson
  89435. erker
  89436. erker
  89437. gerhard
  89438. stereochemistry
  89439. catalysis
  89440. zirconium
  89441. erker
  89442. gerhard
  89443. stereoselective
  89444. synthesis
  89445. zirconium
  89446. compl
  89447. ermakova
  89448. ermal
  89449. ernest
  89450. ernesto
  89451. ernst
  89452. ernst
  89453. recent
  89454. development
  89455. methodology
  89456. ershov
  89457. erwin
  89458. erythrina
  89459. erythro
  89460. erythro-2-amino-12-d
  89461. erythrodiol
  89462. erythromycin
  89463. erythromycin-a
  89464. erythronolide
  89465. erythronolides
  89466. erythrose
  89467. erzhanov
  89468. esack
  89469. escalante
  89470. escape
  89471. eschenmoser
  89472. eschenmoser
  89473. albert
  89474. leowenthal
  89475. chemistry
  89476. potentially
  89477. eschweiler
  89478. escudie
  89479. esipenko
  89480. esipenko
  89481. samarai
  89482. cycloaddition
  89483. nitrile
  89484. oxides
  89485. esker
  89486. esker
  89487. newcomb
  89488. martin
  89489. generation
  89490. nitrogen
  89491. radic
  89492. esmail
  89493. espenson
  89494. espenson
  89495. james
  89496. chemistry
  89497. organochromium
  89498. complexes
  89499. esperamicin
  89500. essam
  89501. essential
  89502. essentials
  89503. essentials
  89504. molecular
  89505. photochemistry
  89506. esser
  89507. esser
  89508. pohlmann
  89509. scharf
  89510. photochemical
  89511. synthesis
  89512. essex
  89513. establish
  89514. establishing
  89515. establishment
  89516. ester
  89517. ester
  89518. cleavages
  89519. sn2-type
  89520. dealkylation
  89521. ester
  89522. enolate
  89523. imine
  89524. condensation
  89525. route
  89526. lactams
  89527. ester
  89528. imine
  89529. condensation
  89530. mediated
  89531. potassium
  89532. butoxide
  89533. ester-derived
  89534. esterases
  89535. esterification
  89536. esterification
  89537. alkylation
  89538. reactions
  89539. employing
  89540. isoureas
  89541. esterifications
  89542. esterifications
  89543. alkylation
  89544. reactions
  89545. employing
  89546. isoureas
  89547. esterolytic
  89548. esterolytic
  89549. lytic
  89550. enzymes
  89551. organic
  89552. synthesis
  89553. esterolytic
  89554. reactivity
  89555. micellar
  89556. assemblies
  89557. cyclode
  89558. esters
  89559. ester
  89560. cleavages
  89561. sn2-type
  89562. dealkylation@
  89563. esterase@
  89564. esters
  89565. esters-promising@
  89566. etherate@
  89567. ethers
  89568. ethoxy@
  89569. evolution
  89570. exchange
  89571. expedient@
  89572. explorations
  89573. non-classical
  89574. area@
  89575. extremly
  89576. chemoselective
  89577. silylformylation
  89578. silylcarbocycli@
  89579. lewis
  89580. proton
  89581. transfer
  89582. reactions@
  89583. krohnke
  89584. synthesis
  89585. specific
  89586. synthesis
  89587. pyridin@
  89588. selection
  89589. capture
  89590. anionic
  89591. carbon@
  89592. facile
  89593. enzymatic
  89594. synthesis
  89595. optically
  89596. active
  89597. hexanediol@
  89598. factors
  89599. famulok
  89600. michale
  89601. nowick
  89602. james
  89603. rebek
  89604. julius
  89605. replicat@
  89606. faulkner
  89607. felix@
  89608. ferrier
  89609. carbohydrate
  89610. boronates
  89611. advances
  89612. field
  89613. tuning
  89614. chemo
  89615. stereoselectivity
  89616. cyclization
  89617. first
  89618. successful
  89619. metal
  89620. coordination
  89621. control
  89622. 13-dipolar
  89623. fiuoride@
  89624. esters
  89625. estimation
  89626. estradiol
  89627. estramycins
  89628. estramycins
  89629. precursor
  89630. family
  89631. derived
  89632. estradi
  89633. eswarakrishnan
  89634. eta'-diiod
  89635. eta-1-acyl
  89636. eta-1-allyl
  89637. eta-5-c5h5
  89638. eta-5-pyrrolyl
  89639. eta-6-arene
  89640. eta2-co2
  89641. eta6-arene
  89642. eterocyclic
  89643. ethan
  89644. ethanediyl
  89645. ethanes
  89646. ethanol
  89647. ethanolamines
  89648. ethene
  89649. ethenes
  89650. ethenoanthracene
  89651. ethenone
  89652. ethenyl
  89653. ethenylbicyclo
  89654. ethenylindoles
  89655. ether
  89656. herates
  89657. ethereal
  89658. etherification
  89659. ethers
  89660. ethers
  89661. ethoxyacetyl
  89662. ethoxybut
  89663. ethoxycarbonyl
  89664. ethoxycarbonylphthal
  89665. ethoxyvinyllithium
  89666. ethoxyvinyllithium
  89667. surprising
  89668. regiochemistry
  89669. aromati
  89670. ethyl
  89671. ethylboron
  89672. ethylene
  89673. ethylenebis
  89674. ethylenebis
  89675. ethylenediamine
  89676. ethylenediazonium
  89677. ethylenes
  89678. ethylenic
  89679. ethylidene
  89680. ethylidenemalonic
  89681. ethynyl
  89682. ethynylarenes
  89683. ethynylbenzenes
  89684. ethynylcyclopropanes
  89685. ethynylphosphonates
  89686. etienne
  89687. etooc
  89688. etraheterosubstitute
  89689. etraheterosubstitute
  89690. ethenes
  89691. etrazines
  89692. etrazines
  89693. pentazines
  89694. etter
  89695. ettore
  89696. euerby
  89697. eugen
  89698. eugene
  89699. eugenio
  89700. eugster
  89701. eugster
  89702. conrad
  89703. marki
  89704. fischer
  89705. edith
  89706. chemistry
  89707. eunice
  89708. eunicellin
  89709. euphorbiacae
  89710. euphorbiaceae
  89711. euranto
  89712. euryfuran
  89713. eusebio
  89714. evaluation
  89715. evaluation
  89716. synthetic
  89717. route
  89718. e-viniferin
  89719. based
  89720. evaluation
  89721. aluminum
  89722. 26-di-tert-butyl-4-m
  89723. evaluation
  89724. effect
  89725. strain
  89726. reactivity
  89727. evaluations
  89728. evanescent
  89729. evans
  89730. evans
  89731. trapping
  89732. 197912
  89733. aldrichimica
  89734. review
  89735. evans
  89736. andrew
  89737. holmes
  89738. andrew
  89739. medium
  89740. nitrogen
  89741. heterocy
  89742. evans-tishchenko
  89743. evanseck
  89744. events
  89745. everett
  89746. evers
  89747. evert
  89748. everyday
  89749. evgenii
  89750. evgeny
  89751. evidence
  89752. rmediate
  89753. configurational
  89754. evidence
  89755. oxocarbenium
  89756. intermediate
  89757. lewis
  89758. evidence
  89759. pericyclic
  89760. stepwise
  89761. processes
  89762. cyclod
  89763. evidence
  89764. occurrence
  89765. substituted
  89766. phthalimides
  89767. evidences
  89768. evolution
  89769. evolution
  89770. evolution
  89771. strategy
  89772. synthesis
  89773. olivomycin
  89774. evolution
  89775. strategy
  89776. total
  89777. synthesis
  89778. streptonigrin
  89779. evolution
  89780. synthetic
  89781. strategy
  89782. total
  89783. synthesis
  89784. evolution
  89785. synthetic
  89786. strategy
  89787. total
  89788. synthesis
  89789. jatroph
  89790. evolutionary
  89791. evolving
  89792. evstigneeva
  89793. ewing`
  89794. ewing
  89795. cyclopentadiene
  89796. second
  89797. supplements
  89798. edite
  89799. ewing
  89800. large
  89801. alicyclic
  89802. systems
  89803. second
  89804. supplements
  89805. ewing
  89806. cycloheptanes
  89807. cyclooctanes
  89808. second
  89809. supplemea
  89810. exafs
  89811. examination
  89812. example
  89813. examples
  89814. excellence
  89815. excellent
  89816. except
  89817. exceptional
  89818. exceptionally
  89819. excesses
  89820. excessive
  89821. exchange
  89822. exchange
  89823. exciplex
  89824. exciplexes
  89825. excitation
  89826. excitatory
  89827. excited
  89828. excluding
  89829. exclusive
  89830. exclusive
  89831. radical
  89832. cyclizations
  89833. silyl
  89834. radicals
  89835. excursions
  89836. executed
  89837. exeitation
  89838. exemplified
  89839. exercise
  89840. exhaustive
  89841. existence
  89842. existing
  89843. exner
  89844. exner
  89845. friedl
  89846. zdenek
  89847. tessek
  89848. laboratory
  89849. transmission
  89850. amino
  89851. borneol
  89852. derived
  89853. oxazolidinone
  89854. selective
  89855. diels-alder
  89856. reactions
  89857. b-unsaturated
  89858. hexac
  89859. exo-anomeric
  89860. exo-enynes
  89861. exo-selective
  89862. exo-selective
  89863. diels-alder
  89864. reactions
  89865. aminocarbene
  89866. complexe
  89867. exocyclic
  89868. expandedQ
  89869. expanded
  89870. systems
  89871. cyclopropenes
  89872. dipolar
  89873. expanded
  89874. systems
  89875. cyclopropenes
  89876. 13-dipolar
  89877. expanding
  89878. expanding
  89879. industrial
  89880. applications
  89881. palladium
  89882. catalysts
  89883. expanding
  89884. roles
  89885. templates
  89886. synthesis
  89887. expanding
  89888. analogy
  89889. between
  89890. phosphorus-carbon
  89891. carbon-c
  89892. expanding
  89893. versatility
  89894. schwartz
  89895. reagent
  89896. hydrozirconati
  89897. expansion
  89898. expansions
  89899. expedient
  89900. expeditious
  89901. expeditious
  89902. synthesis
  89903. azasugars
  89904. double
  89905. reductive
  89906. exper
  89907. experience
  89908. experiment
  89909. experimentai
  89910. experimental
  89911. experimentalist
  89912. experiments
  89913. experiments
  89914. directed
  89915. towards
  89916. synthesis
  89917. anthracyclinon
  89918. explanation
  89919. exploitation
  89920. exploitation
  89921. synthons
  89922. synthesis
  89923. polycyclic
  89924. exploitation
  89925. microbiological
  89926. methods
  89927. synthesis
  89928. exploration
  89929. exploration
  89930. cycloaddition
  89931. reaction
  89932. between
  89933. allyl
  89934. exploration
  89935. cycloaddition
  89936. reaction
  89937. between
  89938. allyls
  89939. exploration
  89940. towards
  89941. pseudomonic
  89942. explorations
  89943. explorations
  89944. non-classical
  89945. explorations
  89946. chalcogen
  89947. heterocycles
  89948. exploratory
  89949. exploratory
  89950. synthetic
  89951. studies
  89952. involving
  89953. tricyclo
  89954. 9.3.3.0
  89955. exploring
  89956. explosives
  89957. expoxidationH
  89958. extended
  89959. extension
  89960. extension
  89961. eschweiler
  89962. clarke
  89963. procedure
  89964. alkyla
  89965. extensions
  89966. extensive
  89967. extensive
  89968. review
  89969. numerous
  89970. heterocyclic
  89971. examples
  89972. extent
  89973. external
  89974. extraction
  89975. extradiol
  89976. extraordinary
  89977. extrathermodynamic
  89978. extreme
  89979. extremely
  89980. extremely
  89981. bulky
  89982. lithium
  89983. trialkylsilyl
  89984. 246-tri-t-butylpheny
  89985. extremely
  89986. chemoselective
  89987. silylformylation
  89988. silylcarbocycl
  89989. extremely
  89990. regioselective
  89991. intramolecular
  89992. silylformylation
  89993. extremly
  89994. extremly
  89995. chemoselective
  89996. silylformylation
  89997. silylcarbocycli
  89998. extrusion
  89999. extrusion
  90000. heterocyclic
  90001. compounds
  90002. systems
  90003. extrusion
  90004. heterocyclic
  90005. compounds
  90006. five-mem
  90007. eyring
  90008. thiourea
  90009. multipurpose
  90010. chemical
  90011. schryver
  90012. boens
  90013. excited
  90014. state
  90015. behavior
  90016. schryver
  90017. boens
  90018. huybrechts
  90019. daemen
  90020. brack
  90021. lewis
  90022. proton
  90023. transfer
  90024. reactions
  90025. heterocycles
  90026. annelatio
  90027. watts
  90028. chemistry
  90029. benzo
  90030. quinoliz
  90031. ziegler
  90032. stereo
  90033. regiochemistry
  90034. claisen
  90035. rearran
  90036. ziegler
  90037. tetrahedron
  90038. symposia
  90039. print
  90040. fringuelli
  90041. taticchi
  90042. wenkert
  90043. fringuelli
  90044. marino
  90045. taticchi
  90046. tellurophene
  90047. relate
  90048. bordwell
  90049. equilibrium
  90050. acidities
  90051. carbon
  90052. acids
  90053. westheimer
  90054. hydrolysis
  90055. phosphate
  90056. esters
  90057. luknitskii
  90058. chemistry
  90059. chloral
  90060. mcquillin
  90061. homogeneous
  90062. catalysis
  90063. ramirez
  90064. maracek
  90065. synthesis
  90066. synthesis
  90067. continuous
  90068. peptide
  90069. synthe
  90070. schmitz
  90071. uncommon
  90072. marine
  90073. steroids
  90074. marine
  90075. natural
  90076. products
  90077. kienzle
  90078. technical
  90079. synth
  90080. krohnke
  90081. synthesis
  90082. specific
  90083. synthesis
  90084. pyridin
  90085. abdel
  90086. galil
  90087. sherif
  90088. elnagdi
  90089. heterocycles
  90090. hauser
  90091. ellenberger
  90092. syntheses
  90093. minisci
  90094. fortschr
  90095. forsch
  90096. recent
  90097. advances
  90098. minisci
  90099. fortschritte
  90100. forschung
  90101. recent
  90102. petit
  90103. organic
  90104. chemistry
  90105. mediated
  90106. piacenti
  90107. bianchi
  90108. carbonylation
  90109. saturated
  90110. oxygenat
  90111. pietra
  90112. total
  90113. synthesis
  90114. wehrli
  90115. organic
  90116. structure
  90117. assignments
  90118. using
  90119. f'urther
  90120. f-block
  90121. fabad
  90122. fabbri
  90123. faber
  90124. faber
  90125. biotransformations
  90126. organic
  90127. chemistry
  90128. springer
  90129. fabian
  90130. fabiana
  90131. fabiana
  90132. hartmann
  90133. light
  90134. absorption
  90135. organic
  90136. colorants
  90137. fabio
  90138. fabre
  90139. selection
  90140. claisen
  90141. rearrangements
  90142. selection
  90143. capture
  90144. anionic
  90145. carbon
  90146. selectivity
  90147. diels
  90148. alder
  90149. additions
  90150. cheletropi
  90151. facelli
  90152. faces
  90153. facet
  90154. facial
  90155. facial
  90156. diastereoselection
  90157. diels-alder
  90158. cycloadditions
  90159. facial
  90160. selective
  90161. diels
  90162. alder
  90163. reactions
  90164. carbometho
  90165. facial
  90166. selectivity
  90167. nucleophilic
  90168. reactions
  90169. spirocyclic
  90170. facially
  90171. facile
  90172. facile
  90173. catalyzed
  90174. cleavage
  90175. acylated
  90176. lactams
  90177. facile
  90178. alkylation
  90179. methyl
  90180. oxazoline
  90181. synthesis
  90182. novel
  90183. facile
  90184. boron
  90185. migration
  90186. during
  90187. hydrozirconation
  90188. alkenylbor
  90189. facile
  90190. cleavage
  90191. dimethylhydrazones
  90192. ketones
  90193. using
  90194. facile
  90195. enzymatic
  90196. synthesis
  90197. optically
  90198. active
  90199. hexanediol
  90200. facile
  90201. formation
  90202. seven
  90203. eight
  90204. membered
  90205. cycloalkenes
  90206. facile
  90207. intramolecular
  90208. acylation
  90209. reactions
  90210. acyloxy
  90211. facile
  90212. intramolecular
  90213. carbolithiation
  90214. reactions
  90215. alkylthio
  90216. facile
  90217. isomerization
  90218. trimethylsilyl
  90219. ketene
  90220. acetals
  90221. facile
  90222. one-pot
  90223. epoxidation-nucleoph
  90224. opening
  90225. sequence
  90226. facile
  90227. preparation
  90228. conjugated
  90229. dienes
  90230. allylic
  90231. alcohol
  90232. facile
  90233. regio
  90234. stereoselective
  90235. diels
  90236. alder
  90237. reactions
  90238. facile
  90239. syntheses
  90240. alkyl
  90241. dihydro
  90242. methylbenzofuran
  90243. facile
  90244. synthesis
  90245. carbonyl
  90246. compounds
  90247. indirect
  90248. facile
  90249. synthesis
  90250. highly
  90251. functionalized
  90252. bicyclo
  90253. 3.2.1
  90254. facile
  90255. triphenylphosphine
  90256. deoxygenation
  90257. benzofuran
  90258. dioxet
  90259. facilitated
  90260. facilitates
  90261. factor
  90262. factors
  90263. factors
  90264. factors
  90265. affecting
  90266. regioselectivity
  90267. intramolecular
  90268. factors
  90269. affecting
  90270. equilibrium
  90271. constant
  90272. homolysis
  90273. factors
  90274. determine
  90275. reactivity
  90276. reactants
  90277. factors
  90278. which
  90279. control
  90280. facial
  90281. selection
  90282. reduction
  90283. facts
  90284. facts
  90285. words
  90286. heteroatomic
  90287. nomenclature
  90288. faehnrich
  90289. fagan
  90290. fagan
  90291. calabrese
  90292. joseph
  90293. malone
  90294. brian
  90295. metal
  90296. complexes
  90297. failed
  90298. failure
  90299. fainleib
  90300. fairing
  90301. falbe
  90302. falck
  90303. falck
  90304. phillipe
  90305. monteil
  90306. fanny
  90307. water
  90308. soluble
  90309. ligands
  90310. faller
  90311. faller
  90312. mazzieri
  90313. nguyen
  90314. tokunaga
  90315. control
  90316. false
  90317. familiar
  90318. families
  90319. family
  90320. famini
  90321. famulok
  90322. famulok
  90323. michale
  90324. nowick
  90325. james
  90326. rebek
  90327. julius
  90328. replicat
  90329. enzymes
  90330. organic
  90331. synthesis
  90332. alteration
  90333. fannicolo
  90334. fanny
  90335. fantasies
  90336. fantoni
  90337. farahat
  90338. farahi
  90339. farcasiu
  90340. farcasiu
  90341. balaban
  90342. alexandru
  90343. bologna
  90344. ursula
  90345. electr
  90346. faresep
  90347. farid
  90348. farina}
  90349. farina
  90350. development
  90351. organometallic
  90352. method
  90353. farneth
  90354. farona
  90355. fasani
  90356. fascinating
  90357. fashion
  90358. isomerisation
  90359. about
  90360. double
  90361. bonds
  90362. fastigilin
  90363. fateley
  90364. fatiadi
  90365. fatiadi
  90366. applications
  90367. malononitrile
  90368. organic
  90369. fatiadi
  90370. delocalized
  90371. dicyanomethylidene
  90372. croconat
  90373. fatima
  90374. fattah
  90375. fatty
  90376. faucon
  90377. faulkner
  90378. faulkner
  90379. faulkner
  90380. marine
  90381. natural
  90382. products
  90383. natural
  90384. faulkner
  90385. marine
  90386. natural
  90387. products
  90388. natural
  90389. faulkner
  90390. marine
  90391. natural
  90392. products
  90393. natural
  90394. product
  90395. reports
  90396. faure
  90397. fausto
  90398. faustov
  90399. favorable
  90400. favorskii
  90401. fawcett
  90402. fawcett
  90403. opallo
  90404. kinetics
  90405. heterogeneous
  90406. electron
  90407. fe/mo/si
  90408. fe/mols
  90409. fe2p2
  90410. feasible
  90411. feathers
  90412. features
  90413. feder
  90414. feder
  90415. structural
  90416. phase
  90417. transition
  90418. dielectric
  90419. prope
  90420. federal
  90421. federovich
  90422. fedin
  90423. fedorov
  90424. fedorova
  90425. fedorovich
  90426. fedotov
  90427. feger
  90428. feher
  90429. fehlhammer
  90430. fehlhammer
  90431. fritz
  90432. marcus
  90433. emergence
  90434. cyano
  90435. fehlner
  90436. feike
  90437. felber
  90438. felix
  90439. felker
  90440. felkin
  90441. femtosecond
  90442. fenced
  90443. fendler
  90444. fendler
  90445. surfactant
  90446. vesicles
  90447. membrane
  90448. mimetic
  90449. agents
  90450. fenestrane
  90451. fenestranes
  90452. fenestranes
  90453. flattening
  90454. tetrahedral
  90455. carbon
  90456. fenical
  90457. fenical
  90458. diterpenoids
  90459. marine
  90460. natural
  90461. products
  90462. chemical
  90463. fenoprofen
  90464. fenselau
  90465. fenton
  90466. ferdinando
  90467. ferenc
  90468. ferguson
  90469. ferguson
  90470. richard
  90471. krajnik
  90472. crabtree
  90473. robert
  90474. develo
  90475. feringa
  90476. feringa
  90477. lange
  90478. jansen
  90479. johan
  90480. johann
  90481. feringa
  90482. jager
  90483. wolter
  90484. lange
  90485. organic
  90486. materials
  90487. fermandjian
  90488. fermentation
  90489. fernando
  90490. ferraboschi
  90491. ferraz
  90492. ferreira
  90493. ferreira
  90494. daneel
  90495. steynberg
  90496. david
  90497. brandt
  90498. vincen
  90499. ferric
  90500. ferrier
  90501. ferrier
  90502. carbohydrate
  90503. boronates
  90504. advances
  90505. ferrier
  90506. robert
  90507. middleton
  90508. sydney
  90509. conversion
  90510. carbohyd
  90511. ferriomethyl
  90512. ferris
  90513. ferrocene
  90514. ferrocenes
  90515. ferrocenophanes
  90516. ferrocenyldiphosphin
  90517. ferrocenyloxazolines
  90518. ferrocenylphosphine
  90519. ferromagnetics
  90520. ferromagnets
  90521. ferrugine
  90522. nenko
  90523. voronkov
  90524. effect
  90525. organi
  90526. fessenden
  90527. fessenden
  90528. fessenden
  90529. trends
  90530. organosilicon
  90531. biologic
  90532. fetizon
  90533. fetzer
  90534. feuer
  90535. fevig
  90536. fferences
  90537. fiandanese
  90538. fiaud
  90539. fiaud
  90540. determination
  90541. absolute
  90542. configurations
  90543. asymme
  90544. fiaud
  90545. kagan
  90546. determinations
  90547. stereochemistry
  90548. fibril
  90549. fibrous
  90550. fication
  90551. fiction
  90552. fiedler
  90553. field
  90554. field
  90555. field
  90556. developments
  90557. synthetic
  90558. organic
  90559. sulfur
  90560. chemis
  90561. field
  90562. lamar
  90563. forty
  90564. years
  90565. hydra
  90566. organosulfur
  90567. chemi
  90568. fields
  90569. fieser
  90570. fieser
  90571. fieser
  90572. fieser's
  90573. reagents
  90574. organic
  90575. synthes
  90576. fieser's
  90577. thomas
  90578. kinetic
  90579. mechanistic
  90580. effects
  90581. fifth
  90582. fifty
  90583. fifty
  90584. years
  90585. radicals
  90586. filipp
  90587. filippova
  90588. filippovich
  90589. filler
  90590. filler
  90591. reactions
  90592. organic
  90593. compounds
  90594. xenon
  90595. fluorides
  90596. filler
  90597. robert
  90598. organofluorine
  90599. compounds
  90600. medicinal
  90601. chemi
  90602. fillmore
  90603. fillol
  90604. filmsK
  90605. fimuo
  90606. final
  90607. finally
  90608. findeis
  90609. findeisen
  90610. findings
  90611. feathers
  90612. birds
  90613. reaction
  90614. modern
  90615. tuning
  90616. chemo
  90617. stereoselectivity
  90618. cyclization
  90619. finet
  90620. finley
  90621. finley
  90622. triazoles
  90623. chemistry
  90624. heterocyclic
  90625. compou
  90626. finzi
  90627. firestone
  90628. firouzabadi
  90629. first
  90630. first
  90631. cycloaddition
  90632. reaction
  90633. between
  90634. vinyl
  90635. fischer
  90636. first
  90637. diels
  90638. alder
  90639. reactions
  90640. enantiomerically
  90641. first
  90642. enantioselective
  90643. synthesis
  90644. mikanecic
  90645. diels
  90646. first
  90647. examples
  90648. episulfone
  90649. reactions
  90650. sulfonyl
  90651. carbanio
  90652. first
  90653. heterocycloaddition
  90654. generated
  90655. tolylsulf
  90656. first
  90657. stereoselective
  90658. synthesis
  90659. arene
  90660. chromium
  90661. complexes
  90662. first
  90663. stereoselective
  90664. synthesis
  90665. arene
  90666. chromium
  90667. tricarbony
  90668. first
  90669. successful
  90670. metal
  90671. coordination
  90672. control
  90673. 13-dipolar
  90674. first
  90675. total
  90676. synthesis
  90677. taxol
  90678. functionalization
  90679. first
  90680. total
  90681. synthesis
  90682. taxol
  90683. completion
  90684. first
  90685. total
  90686. synthesis
  90687. benzopyranobenazepin
  90688. alkaloid
  90689. fischer
  90690. fischer
  90691. isomerases
  90692. their
  90693. effectors
  90694. angew
  90695. fischer
  90696. industrial
  90697. applications
  90698. photochemical
  90699. syntheses
  90700. fischer
  90701. olivier
  90702. fischer
  90703. biogenesis
  90704. chemi
  90705. fischer
  90706. weitz
  90707. preparation
  90708. reactions
  90709. cyclic
  90710. fischer's
  90711. fischer-indole
  90712. fischer-tropsch
  90713. fischler
  90714. fisher
  90715. fission
  90716. fiuid
  90717. fiuoride
  90718. five-membered
  90719. membered
  90720. cyclic
  90721. phosphorylating
  90722. reagents
  90723. related
  90724. five-membered
  90725. heteroaromatic
  90726. rings
  90727. intermediates
  90728. organ
  90729. five-membered
  90730. rings
  90731. containing
  90732. selenium
  90733. tellurium
  90734. five-membered
  90735. rings
  90736. containing
  90737. three
  90738. oxygen
  90739. sulfur
  90740. atoms
  90741. five-membered
  90742. rings
  90743. oxygen
  90744. sulfur
  90745. least
  90746. five-membered
  90747. selenium-nitrogen
  90748. heterocycles
  90749. five-membered-ring
  90750. fixation
  90751. fk-506
  90752. fk506
  90753. fk506/fkbp
  90754. oroheterocyclic
  90755. compounds
  90756. synthesis
  90757. reactions
  90758. commerc
  90759. flament
  90760. flash
  90761. flash
  90762. photolytic
  90763. generation
  90764. study
  90765. reactive
  90766. species
  90767. flash
  90768. vacuum
  90769. pyrolysis
  90770. versatile
  90771. method
  90772. organic
  90773. chemist
  90774. flash
  90775. vacuum
  90776. pyrolysis
  90777. alkoxycarbonyl/sulfi
  90778. stabilised
  90779. flash
  90780. vacuum
  90781. pyrolysis
  90782. cyclopropene
  90783. anthracene
  90784. adducts
  90785. flash
  90786. vacuum
  90787. thermolysis
  90788. review
  90789. flash-vacuum
  90790. flashphotolysis
  90791. flask
  90792. flattening
  90793. flavanoids
  90794. flavin
  90795. flavins
  90796. flavocoenzyme
  90797. flavonoid
  90798. flavonoids
  90799. flavoprotein
  90800. flavor
  90801. flavors
  90802. flavylium
  90803. fleet
  90804. fleischer
  90805. fleming
  90806. fleming
  90807. silicon
  90808. compounds
  90809. organic
  90810. synthesi@
  90811. fluoborates
  90812. fluorinated
  90813. ometallics
  90814. perfluoroalkyl
  90815. functionalize@
  90816. fluorine
  90817. fluoro-substituted
  90818. aminoacids
  90819. fodor
  90820. dharanipragada
  90821. tropane
  90822. alkaloids
  90823. natural
  90824. product
  90825. forbidden@
  90826. formal
  90827. formal
  90828. cycloadditions
  90829. allyl
  90830. silanes
  90831. benz@
  90832. formation
  90833. formation
  90834. carbon-carbon
  90835. carbon-heteroatom
  90836. bonds
  90837. formation
  90838. oxatricyclo
  90839. 3.2.1.0
  90840. octane
  90841. system
  90842. formosinho@
  90843. forschung
  90844. fraga
  90845. natural
  90846. sesquiterpenoids
  90847. natural
  90848. frameworks@
  90849. franssen
  90850. boavida
  90851. santos
  90852. camacho
  90853. mondril
  90854. radical
  90855. chain
  90856. reactions
  90857. involving
  90858. alkyl
  90859. alkenylmerc
  90860. freeman
  90861. properties
  90862. reactions
  90863. ylidenemalononitrile
  90864. frequency@
  90865. fleming
  90866. silicon
  90867. compounds
  90868. organic
  90869. synthesi
  90870. fletcher
  90871. fletcher
  90872. siegrist
  90873. olefin
  90874. synthesis
  90875. anils
  90876. flexibility
  90877. flexible
  90878. flexible
  90879. stereoselective
  90880. construction
  90881. polypropionate
  90882. flexible
  90883. molecules
  90884. definite
  90885. shape-conformation
  90886. design
  90887. flexibly
  90888. flitsch
  90889. flitsch
  90890. kramer
  90891. cyclazines
  90892. related
  90893. bridged
  90894. annulene
  90895. flood
  90896. flood
  90897. stereochemistry
  90898. reactions
  90899. transition
  90900. metal
  90901. florent
  90902. flores
  90903. florida
  90904. floss
  90905. floss
  90906. heinz
  90907. sungsook
  90908. chiral
  90909. methyl
  90910. groups
  90911. small
  90912. floss
  90913. heinz
  90914. strohl
  90915. william
  90916. genetic
  90917. engineering
  90918. hybrid
  90919. flower
  90920. flowering
  90921. flowers
  90922. flowing
  90923. floyd
  90924. fluctuations
  90925. fluid
  90926. fluids
  90927. fluka
  90928. fluoborates
  90929. fluoborates
  90930. fluor
  90931. fluoralkenylphosphon
  90932. fluoranthene
  90933. fluorene
  90934. fluorenyl
  90935. fluorescence
  90936. fluorescens
  90937. fluorescent
  90938. fluorescent
  90939. photoinduced
  90940. electron
  90941. transfer
  90942. sensors
  90943. fluori
  90944. fluoride
  90945. fluoride
  90946. catalyzed
  90947. intramolecular
  90948. denitro
  90949. cyclization
  90950. fluoride
  90951. organic
  90952. synthesis
  90953. fluoride
  90954. nucleophile
  90955. leaving
  90956. group
  90957. aromati
  90958. fluoride
  90959. promoted
  90960. azomethine
  90961. generation
  90962. fluoride
  90963. promoted
  90964. reaction
  90965. polyfluoro
  90966. propenyl
  90967. fluorides
  90968. fluorin
  90969. fluorinated
  90970. fluorinated
  90971. ometallics
  90972. perfluoroalkyl
  90973. functionalize
  90974. fluorinated
  90975. organic
  90976. peroxides
  90977. their
  90978. decomposition
  90979. behavior
  90980. fluorinated
  90981. organometallics
  90982. vinyl
  90983. alkynyl
  90984. allyl
  90985. benzyl
  90986. propa
  90987. fluorinated
  90988. peniciilins
  90989. other
  90990. lactams
  90991. chemistry
  90992. fluorinated
  90993. vinyl
  90994. carbamates
  90995. carbamoyloxy
  90996. allylsilanes
  90997. fluorinating
  90998. fluorination
  90999. fluorination
  91000. sulfur
  91001. tetrafluoride
  91002. fluorination
  91003. organic
  91004. compounds
  91005. fluorosulfuranes
  91006. fluorination
  91007. diethylaminosulfur
  91008. trifluorid
  91009. related
  91010. fluorination
  91011. sulfur
  91012. tetrafluoride
  91013. boswell
  91014. fluorinations
  91015. fluorine
  91016. fluorine
  91017. fluorine
  91018. chemistry
  91019. without
  91020. fluorine
  91021. substituent
  91022. effects
  91023. fluorine
  91024. bioorganic
  91025. chemistry
  91026. fluorine
  91027. total
  91028. synthesis
  91029. dl-b-amyrin
  91030. fluorine
  91031. substituted
  91032. analogs
  91033. nucleic
  91034. components
  91035. fluorine-containing
  91036. fluorine-containing
  91037. aromatic
  91038. amino
  91039. acids
  91040. fluorine-containing
  91041. bioactive
  91042. benzimidazoles
  91043. fluorine-containing
  91044. ketimines
  91045. fluorine-containing
  91046. molecules
  91047. structure
  91048. reactivity
  91049. synthesis
  91050. fluorine-directed
  91051. fluorine-directed
  91052. nazarov
  91053. cyclizations
  91054. controlled
  91055. synthesi
  91056. fluorine-stabilized
  91057. fluorine-stabilized
  91058. sulfur-carbon
  91059. multiple
  91060. bonds
  91061. fluorinnting
  91062. fluoro
  91063. fluoro-organic
  91064. fluoro-substituted
  91065. fluoro-substituted
  91066. aminoacids
  91067. fluoro-substituted
  91068. aminoacids
  91069. fluoroalkanesulfonyl
  91070. fluoroalkenyl
  91071. fluoroallene
  91072. fluoroaromatic
  91073. fluoroaromatic
  91074. compounds
  91075. synthesis
  91076. reactions
  91077. commercial
  91078. fluoroaromatics
  91079. fluorobenzenes
  91080. fluorocarbanions
  91081. fluorocarbons
  91082. fluorocarbonyl
  91083. fluoroenylmethoyloxy
  91084. fluoroheterocyclic
  91085. fluoroimines
  91086. fluoroketones
  91087. fluoromethylenes
  91088. fluoromethylketones
  91089. fluoronitroso
  91090. fluoroolefins
  91091. fluoroorganicl
  91092. fluoropyrrole
  91093. fluoropyrroles
  91094. fluorosilicate
  91095. fluorospectrochemist
  91096. fluorosubstituted
  91097. fluorosulfur
  91098. fluorosulfuranes
  91099. fluorosulphates
  91100. fluoroxy
  91101. fluxional
  91102. flygare
  91103. focus
  91104. fodor
  91105. fodor
  91106. dharanipragada
  91107. tropane
  91108. alkaloids
  91109. natural
  91110. fodor
  91111. dharanipragada
  91112. tropane
  91113. alkaloids
  91114. natural
  91115. product
  91116. fodor
  91117. dharanipragada
  91118. tropane
  91119. alkaloids
  91120. natural
  91121. product
  91122. fodor
  91123. nagubandi
  91124. correlation
  91125. braun
  91126. ritter
  91127. fokin
  91128. fokin
  91129. tyutin
  91130. chkanikov
  91131. chemistry
  91132. perfluo
  91133. fokin
  91134. stolyarov
  91135. organic
  91136. fluoroimines
  91137. folding
  91138. folest
  91139. foley
  91140. folkers
  91141. folkin
  91142. follet
  91143. followed
  91144. following
  91145. fomannosin
  91146. fonskii
  91147. fontain
  91148. fontana
  91149. foods
  91150. foote
  91151. foote
  91152. quenching
  91153. singlet
  91154. oxygen
  91155. singlet
  91156. oxygen
  91157. foote
  91158. christopher
  91159. photophysical
  91160. photochemical
  91161. properti
  91162. footsteps
  91163. formal
  91164. formal
  91165. cycloadditions
  91166. allyl
  91167. silanes
  91168. formal
  91169. synthesis
  91170. rac-morphine
  91171. formaldehyde
  91172. formalism
  91173. formally
  91174. formamide
  91175. formamides
  91176. formamidine
  91177. formamidine
  91178. versatile
  91179. protecting
  91180. group
  91181. primary
  91182. formamidines
  91183. formamidines
  91184. precursors
  91185. alpha
  91186. amino
  91187. carbanions
  91188. formamidines
  91189. precursors
  91190. alpha-amino
  91191. carbanions
  91192. format
  91193. formates
  91194. formatio
  91195. formationF
  91196. formation
  91197. formation
  91198. formation
  91199. addition
  91200. reactions
  91201. ethers
  91202. formation
  91203. breaking
  91204. formation
  91205. breaking
  91206. bonds
  91207. oxidative
  91208. additi
  91209. formation
  91210. cyclization
  91211. thioamides
  91212. novel
  91213. b-lacta
  91214. formation
  91215. further
  91216. transformations
  91217. 11-dihalocyclopropa
  91218. formation
  91219. reactions
  91220. organosulfur
  91221. organoselenium
  91222. formation
  91223. structure
  91224. ozonides
  91225. formation
  91226. acylindoles
  91227. acylindoles
  91228. formation
  91229. strained
  91230. triazapentalenoinden
  91231. skeleton
  91232. formation
  91233. angularly
  91234. fused
  91235. triquinanes
  91236. successive
  91237. formation
  91238. carbon
  91239. carbon
  91240. solid
  91241. support
  91242. application
  91243. formation
  91244. carbon
  91245. carbon
  91246. bonds
  91247. allylnickel
  91248. compound
  91249. formation
  91250. carbon
  91251. heteroatom
  91252. bonds
  91253. radical
  91254. chain
  91255. formation
  91256. carbon-carbon
  91257. carbon-heteroatom
  91258. bonds
  91259. formation
  91260. carbon-carbon
  91261. bonds
  91262. using
  91263. organoboranes
  91264. formation
  91265. carbon-carbon
  91266. bonds
  91267. using
  91268. zirconocene
  91269. butene
  91270. formation
  91271. carbon-carbon
  91272. bonds
  91273. allylnickel
  91274. compounds
  91275. formation
  91276. carbon-heteroatom
  91277. bonds
  91278. radical
  91279. chain
  91280. formation
  91281. convenient
  91282. chiral
  91283. intermediates
  91284. carbohydra
  91285. formation
  91286. cycloadducts
  91287. trans
  91288. configurated
  91289. ester
  91290. formation
  91291. diazoketones
  91292. azines
  91293. improved
  91294. oxidation
  91295. formation
  91296. enolates
  91297. formation
  91298. heterocycles
  91299. iminium
  91300. salts
  91301. cyclization
  91302. formation
  91303. highly
  91304. substituted
  91305. cyclopentanes
  91306. radical
  91307. formation
  91308. steroids
  91309. derivatives
  91310. beckmann
  91311. formation
  91312. homo-aza-steroids
  91313. derivatives
  91314. beckmann
  91315. formation
  91316. organoperoxides
  91317. superoxide
  91318. formation
  91319. radical
  91320. functions
  91321. conservation
  91322. carbon
  91323. formation
  91324. stable
  91325. isolable
  91326. conjugated
  91327. primary
  91328. enamines
  91329. formation
  91330. oxatricyclo
  91331. 3.2.1.0
  91332. octane
  91333. system
  91334. formation
  91335. unsaturated
  91336. esters
  91337. single
  91338. electron
  91339. trans
  91340. formation-reactivity
  91341. formation-scissor-li
  91342. formations
  91343. formations
  91344. cycloadduct
  91345. electron
  91346. transfer
  91347. formazans
  91348. formed
  91349. formic
  91350. forming
  91351. forms
  91352. formula
  91353. formulas
  91354. formyl
  91355. formylating
  91356. formylation
  91357. formylation
  91358. unsubstituted
  91359. oxazole
  91360. preparation
  91361. formylbenzoyl
  91362. formylmaleanilates
  91363. formylphosphonate
  91364. forsch
  91365. forschung
  91366. forschung
  91367. forschungs
  91368. forsh
  91369. forskolin
  91370. forskolin
  91371. congeners
  91372. forster
  91373. forster
  91374. mechanistic
  91375. pathways
  91376. catalytic
  91377. carbonylatio
  91378. forstmeyer
  91379. forsyth
  91380. fortachritte
  91381. fortschr
  91382. fortschritte
  91383. forty
  91384. forty
  91385. years
  91386. hydra
  91387. organosulfur
  91388. chemistry
  91389. forty
  91390. years
  91391. hydride
  91392. reductions
  91393. forty-five
  91394. forty-five
  91395. years
  91396. hydra
  91397. organosulfur
  91398. chemistry
  91399. fossey
  91400. fossey
  91401. jacques
  91402. lefort
  91403. daniel
  91404. sorba
  91405. janine
  91406. peracids
  91407. fossils
  91408. foster
  91409. fotsch
  91410. foundations
  91411. fountain
  91412. membered
  91413. peroxides
  91414. excited
  91415. state
  91416. equivalents
  91417. four-electron
  91418. four-electron
  91419. alkyne
  91420. ligands
  91421. molybdenum
  91422. tungsten
  91423. four-membered
  91424. four-membered
  91425. cyclic
  91426. nitrones
  91427. synthesis
  91428. reactivity
  91429. four-membered
  91430. heterocycles
  91431. containing
  91432. phosphorus
  91433. four-membered
  91434. compounds
  91435. containing
  91436. methylene
  91437. cyclob
  91438. four-membered
  91439. rings
  91440. isocyanides-recent
  91441. advances
  91442. four-membered
  91443. rings
  91444. heteroatoms
  91445. fused-r
  91446. four-to
  91447. fourfold
  91448. fourier
  91449. photoexcited
  91450. states
  91451. organic
  91452. anions
  91453. marye
  91454. experimental
  91455. probes
  91456. excited
  91457. fraaer
  91458. fraga
  91459. fraga
  91460. natural
  91461. sesquiterpenoids
  91462. natural
  91463. fraga
  91464. natural
  91465. sesquiterpenoids
  91466. 19929
  91467. natural
  91468. fraga
  91469. natural
  91470. sesquiterpenoids
  91471. natural
  91472. product
  91473. reports
  91474. fragment
  91475. fragmentation
  91476. fragmentation
  91477. alkoxy
  91478. radicals
  91479. tandem
  91480. fragmentation
  91481. fragmentation
  91482. carbohydrate
  91483. anomeric
  91484. alkoxy
  91485. radicals
  91486. tande
  91487. fragmentation
  91488. reactions
  91489. fragmentations
  91490. fragmentations
  91491. photoinduced
  91492. electron
  91493. transfer
  91494. fundamental
  91495. fragments
  91496. fragrance
  91497. fragrances
  91498. fragrant
  91499. frame
  91500. framework
  91501. frameworks
  91502. franc
  91503. franca
  91504. france
  91505. francesca
  91506. franceschi
  91507. francesco
  91508. francesconi
  91509. franceso
  91510. francheschi
  91511. francis
  91512. francisco
  91513. franck
  91514. franck
  91515. building
  91516. blocks
  91517. natural
  91518. products
  91519. biosynthesi
  91520. franck
  91521. mitomycin
  91522. antibiotics
  91523. progress
  91524. franco
  91525. francois
  91526. francoise
  91527. franek
  91528. franek
  91529. walter
  91530. tetrathianes
  91531. syntheses
  91532. reactions
  91533. franek
  91534. walter
  91535. tetrathianes
  91536. structure
  91537. spectroscop
  91538. frank
  91539. franklin
  91540. frans
  91541. franssen
  91542. franssen
  91543. boavida
  91544. santos
  91545. camacho
  91546. mondril
  91547. frantisek
  91548. franz
  91549. franzini
  91550. fraser
  91551. fraser
  91552. anderson
  91553. carbohydrate
  91554. derivatives
  91555. fraser
  91556. merritt
  91557. robert
  91558. handlon
  91559. anthony
  91560. andrews
  91561. fraser
  91562. udodong
  91563. zufan
  91564. ottosson
  91565. hakan
  91566. merri
  91567. frauenrach
  91568. frauenrath
  91569. saxton
  91570. chemistry
  91571. cyclooctatetraene
  91572. freccero
  91573. frechet
  91574. frechet
  91575. synthesis
  91576. applications
  91577. organic
  91578. polymers
  91579. fredericamycin
  91580. frederick
  91581. fredric
  91582. energy
  91583. calculations
  91584. breakthrough
  91585. modeling
  91586. organic
  91587. radical
  91588. addition
  91589. alkanethiols
  91590. alkynes
  91591. rearrangeme
  91592. radical
  91593. additions
  91594. olefins
  91595. carbon
  91596. carbon
  91597. radical
  91598. additions
  91599. olefins
  91600. carbon-carbon
  91601. radical
  91602. based
  91603. annulation
  91604. alkenes
  91605. yielding
  91606. fused
  91607. radical
  91608. chain
  91609. processes
  91610. aliphatic
  91611. systems
  91612. involving
  91613. radical
  91614. chain
  91615. reactions
  91616. organic
  91617. chemistry
  91618. radical
  91619. chain
  91620. reactions
  91621. involving
  91622. alkyl
  91623. alkenylmerc
  91624. radical
  91625. chain
  91626. reactions
  91627. involving
  91628. alkyl
  91629. alkenylmerc
  91630. radical
  91631. fragmentation
  91632. photoadduct
  91633. derivatives
  91634. radical
  91635. macrocyclization
  91636. radical
  91637. mediated
  91638. methylenecyclopentan
  91639. annulations
  91640. radical
  91641. reactions
  91642. fragmentation
  91643. rearrangement
  91644. radical
  91645. reactions
  91646. involving
  91647. saturated
  91648. unsaturated
  91649. radical
  91650. reactions
  91651. organomercurials
  91652. radical
  91653. rearrangement
  91654. uracil
  91655. derivatives
  91656. radical
  91657. rearrangement
  91658. alkenyl
  91659. epoxy
  91660. silanes
  91661. isolatio
  91662. radical
  91663. thermochemistry
  91664. radical
  91665. tritylation
  91666. unsaturated
  91667. carboxylic
  91668. radical-mediated
  91669. expansion
  91670. related
  91671. annulations
  91672. radicals
  91673. chemistry
  91674. biology
  91675. free-radical
  91676. free-radical
  91677. chain
  91678. reactions
  91679. organic
  91680. chemistr
  91681. freedman
  91682. freely
  91683. freeman
  91684. freeman
  91685. properties
  91686. reactions
  91687. ylidenemalononitrile
  91688. freeman
  91689. reactions
  91690. malononitrile
  91691. derivatives
  91692. synthe
  91693. freeman
  91694. fillmore
  91695. aregullin
  91696. manuel
  91697. rodriguez
  91698. naturally
  91699. freeman
  91700. peter
  91701. hatlevig
  91702. susan
  91703. photochemistry
  91704. polyh
  91705. freeman
  91706. richard
  91707. haynes
  91708. richard
  91709. loughlin
  91710. wendy
  91711. mitchell
  91712. freiberg
  91713. freidinger
  91714. freidlina
  91715. freidlina
  91716. terent'ev
  91717. rearrangement
  91718. short
  91719. lived
  91720. freidlina
  91721. terent'ev
  91722. isomerization
  91723. unstable
  91724. freifelder
  91725. freifelder
  91726. catalytic
  91727. hydrogenation
  91728. organic
  91729. synthesis
  91730. freimanis
  91731. fremy's
  91732. french
  91733. frenkel
  91734. frenkel
  91735. michael
  91736. thermochemistry
  91737. equilibria
  91738. organic
  91739. frenna
  91740. frequencies
  91741. fresenius
  91742. fretz
  91743. freund
  91744. frick
  91745. fridamycin
  91746. fridamycin
  91747. fridkin
  91748. fridkin
  91749. polymeric
  91750. reagents
  91751. peptide
  91752. synthesis
  91753. peptid
  91754. fridland
  91755. fridland
  91756. chernokal'skii
  91757. structure
  91758. reactivity
  91759. fridman
  91760. fridman
  91761. surkov
  91762. novikov
  91763. chemistry
  91764. halogenoni
  91765. friebe
  91766. friedQ
  91767. fried
  91768. sherma
  91769. layer
  91770. chromatography
  91771. techniques
  91772. friedel
  91773. friedel
  91774. crafts
  91775. transannular
  91776. alkylation
  91777. aromatic
  91778. compounds
  91779. friedel-crafts
  91780. friedel-crafts
  91781. acylation
  91782. little
  91783. friedel-crafts
  91784. alkylations
  91785. frieder
  91786. friedl
  91787. friedlander
  91788. friedlina
  91789. friedrich
  91790. friedrich
  91791. holger
  91792. halogenoalkyl
  91793. complexes
  91794. friedrichsen
  91795. friedrichsen
  91796. benzo
  91797. furans
  91798. 26135
  91799. advances
  91800. heteroc
  91801. friedrichsen
  91802. bottcher
  91803. recent
  91804. developments
  91805. chemist
  91806. friend
  91807. friendly
  91808. fries
  91809. frimer
  91810. frimer
  91811. photosensitized
  91812. oxidation
  91813. strained
  91814. olefins
  91815. frimer
  91816. reactions
  91817. singlet
  91818. oxygen
  91819. olefins
  91820. fringuelli
  91821. fringuelli
  91822. francesco
  91823. minuti
  91824. lucio
  91825. pizzo
  91826. ferdinando
  91827. taticchi
  91828. fritsch
  91829. fritz
  91830. froessl
  91831. frogs
  91832. frohning
  91833. frohning
  91834. fischer
  91835. tropsch
  91836. synthesis
  91837. syntheses
  91838. frolova
  91839. frolow
  91840. atoms
  91841. bonds
  91842. three-dimensional
  91843. atomic
  91844. coordinates
  91845. clasical
  91846. chirality
  91847. topologically
  91848. chiral
  91849. catenands
  91850. equilibrium
  91851. acidities
  91852. radical
  91853. stabilization
  91854. energies
  91855. polyenals
  91856. retinal
  91857. electron-spin-echo
  91858. study
  91859. push-pull-substitute
  91860. allenes
  91861. tetra-nuclear
  91862. chelate
  91863. amino-b
  91864. hydroxyacids
  91865. diamino
  91866. hydroxyacid
  91867. silabenzene
  91868. cyclopropanylidene
  91869. silicon-hydrogen
  91870. carbon-hydrogen
  91871. activation
  91872. silylcarbinols
  91873. silaethylenes
  91874. froman
  91875. froman
  91876. synthesis
  91877. reactions
  91878. prismanes
  91879. recen
  91880. frommer
  91881. front
  91882. frontier
  91883. frontiers
  91884. fronza
  91885. fronza
  91886. giovanni
  91887. fuganti
  91888. claudio
  91889. grasselli
  91890. piero
  91891. pedrocchi
  91892. frost
  91893. frost
  91894. christopher
  91895. howarth
  91896. joshua
  91897. williams
  91898. jonathan
  91899. selec
  91900. fruchier
  91901. fructose
  91902. frunze
  91903. frunze
  91904. kurashev
  91905. kotel'nikov
  91906. volkova
  91907. activato
  91908. albert
  91909. electrochemistry
  91910. organic
  91911. synthesis
  91912. fryer
  91913. fryer
  91914. bicyclic
  91915. diazepines
  91916. diazepines
  91917. additi
  91918. fryxell
  91919. fryzuk
  91920. harvey
  91921. dehydrogenation
  91922. polycyclic
  91923. hydroaromati
  91924. xiaoyong
  91925. james
  91926. synthesis
  91927. polyquinanes
  91928. fubrhop
  91929. fubrhop
  91930. jurgen
  91931. heinrich
  91932. reinhard
  91933. monolayer
  91934. lipid
  91935. membra
  91936. silylcarbinols
  91937. silaethylenes@
  91938. fuchigami@
  91939. fukuyama
  91940. tohru
  91941. synthesis
  91942. naphthyridinomycin
  91943. advances
  91944. function
  91945. functional
  91946. group
  91947. assisted
  91948. clathrate
  91949. formation-scissor-li
  91950. functional-groups@
  91951. functionality@
  91952. diates@
  91953. fundamentals
  91954. furanosesquiterpene
  91955. furaquinocin@
  91956. furlong@
  91957. fused
  91958. fused
  91959. oxacycle
  91960. synthesis
  91961. radical
  91962. cyclization
  91963. alkoxy@
  91964. prakash
  91965. synthesis
  91966. perfl@
  91967. kunesch
  91968. poupat
  91969. biosynthetic
  91970. studies
  91971. precurs
  91972. newkome
  91973. baker
  91974. proced
  91975. klumpp
  91976. examples
  91977. g-unsaturated@
  91978. ganem
  91979. glucose
  91980. aromatics
  91981. recent
  91982. developments
  91983. gasteiger
  91984. ihlenfeldt
  91985. collection
  91986. computer
  91987. gelbard@
  91988. general
  91989. generation@
  91990. fuchigamil
  91991. fuchigami
  91992. electrochemical
  91993. reactions
  91994. fluoroorganic
  91995. compol
  91996. fuchigami
  91997. toshio
  91998. selective
  91999. anodic
  92000. partial
  92001. fluorination
  92002. fuchs
  92003. fuchs
  92004. conformations
  92005. membered
  92006. rings
  92007. topic
  92008. fuerstner
  92009. fuganti
  92010. fuhrhop
  92011. fuhrhop
  92012. jurgen
  92013. penzlin
  92014. gustav
  92015. organic
  92016. synthesis
  92017. concepts
  92018. chiral
  92019. nitro
  92020. olefins
  92021. enantioselective
  92022. kaoru
  92023. asymmetric
  92024. creation
  92025. quaternary
  92026. carbon
  92027. centers
  92028. fujihara
  92029. fujihara
  92030. hisashi
  92031. furukawa
  92032. naomichi
  92033. disulfide
  92034. cations
  92035. fujii
  92036. fujimoto
  92037. fujimoto-belleau
  92038. fujise
  92039. fujita
  92040. fujita
  92041. shinsaku
  92042. symmetry
  92043. combinatorial
  92044. enumeration
  92045. fujiwara
  92046. fukahon
  92047. fukai
  92048. fukazawa
  92049. fukuda
  92050. fukui
  92051. fukumoto
  92052. fukushima
  92053. fukuto
  92054. fukuyama
  92055. fukuyama
  92056. tohru
  92057. synthesis
  92058. naphthyridinomycin
  92059. advances
  92060. fuller
  92061. fulleranes
  92062. fullercages
  92063. fullercages
  92064. without
  92065. carbon-fulleranes
  92066. fuller
  92067. space-fille
  92068. fullerene
  92069. fullerene
  92070. chemistry
  92071. fullerene
  92072. structure
  92073. dynami
  92074. magnetic
  92075. resonance
  92076. potpou
  92077. fullerenes
  92078. fulleroida
  92079. fulleroids
  92080. fully
  92081. fulminic
  92082. fulminic
  92083. fulvalene
  92084. fulvalenes
  92085. fulvenes
  92086. fulvio
  92087. fumctional
  92088. fumdamentals
  92089. fumie
  92090. fumihisa
  92091. fumio
  92092. fumitaka
  92093. fumiyuki
  92094. fumonisins
  92095. funayama
  92096. funayama
  92097. hikino
  92098. hypotensive
  92099. principles
  92100. plants
  92101. 19811
  92102. function
  92103. function
  92104. functiona
  92105. functionai
  92106. functional
  92107. ional
  92108. group
  92109. assisted
  92110. clathrate
  92111. formation-scissor-li
  92112. functional
  92113. group
  92114. conversions
  92115. using
  92116. phosphorus
  92117. reagents
  92118. functional
  92119. group
  92120. conversions
  92121. using
  92122. phosphorus
  92123. reagents
  92124. functional
  92125. group
  92126. manipulation
  92127. reactions
  92128. organoselenium
  92129. functional
  92130. group
  92131. manipulations
  92132. using
  92133. organoselenium
  92134. reagents
  92135. functional
  92136. group
  92137. transformations
  92138. allyl
  92139. rearrangement
  92140. functional
  92141. group
  92142. transformations
  92143. carbonyl
  92144. derivatives
  92145. functional-groups
  92146. functionalgroups
  92147. functionalisation
  92148. functionalisation
  92149. methoxy
  92150. methylpyridine
  92151. functionalised
  92152. functionalised
  92153. nitroalkenes
  92154. useful
  92155. reagents
  92156. alkyl
  92157. functionalities
  92158. ionality
  92159. functionalization
  92160. functionalization
  92161. alkenes
  92162. cycloaddition
  92163. cycloreversi
  92164. functionalization
  92165. alkynes
  92166. enynes
  92167. arynes
  92168. using
  92169. organoz
  92170. functionalization
  92171. crown
  92172. ethers
  92173. calixarenes
  92174. applic
  92175. functionalization
  92176. terocycles
  92177. pd-catalyzed
  92178. functionalization
  92179. dihydrothiazine
  92180. cephem
  92181. functionalizations
  92182. functionalized
  92183. functionalized
  92184. cyclopropenes
  92185. synthetic
  92186. intermediates
  92187. functionalized
  92188. nitroalkanes
  92189. useful
  92190. reagents
  92191. alkyl
  92192. functionalized
  92193. tetraazamacrocycles
  92194. ligands
  92195. aspects
  92196. functionalized
  92197. tetracyanoquinodimet
  92198. electron
  92199. acceptors
  92200. suita
  92201. functionalizing
  92202. functionally
  92203. functions
  92204. fundamenta
  92205. fundamental
  92206. fundamentals
  92207. fundamentals
  92208. fundamentals
  92209. silicon
  92210. chemistry
  92211. molecular
  92212. states
  92213. silico
  92214. fundementals
  92215. fundementals
  92216. peptide
  92217. synthesis
  92218. construction
  92219. carboxamid
  92220. fungal
  92221. fungi
  92222. fungicidal
  92223. fungus
  92224. funicello
  92225. funicello
  92226. maria
  92227. spagnolo
  92228. piero
  92229. zanirato
  92230. paolo
  92231. intramolecular
  92232. vollherdt
  92233. thermal
  92234. photochemical
  92235. transitio
  92236. funke
  92237. furakawa
  92238. furan
  92239. furan
  92240. photoreactions
  92241. benzylfuran
  92242. furan
  92243. annulation
  92244. strategy
  92245. efficient
  92246. synthesis
  92247. fused
  92248. furane
  92249. furanocembranolide
  92250. furanoditerpenoids
  92251. furanohydrophenanthr
  92252. furanones
  92253. furanosesquiterpene
  92254. furanosesquiterpene
  92255. furanosesquiterpene
  92256. synthesis
  92257. furanosesquiterpene
  92258. synthesis
  92259. updated
  92260. review
  92261. furanosyl
  92262. furanoterpenes
  92263. furans
  92264. furans
  92265. benzo
  92266. derivatives
  92267. structure
  92268. furans
  92269. their
  92270. benzo
  92271. derivatives
  92272. reactivity
  92273. furans
  92274. their
  92275. benzo
  92276. derivatives
  92277. synthesis
  92278. applica
  92279. furans
  92280. novel
  92281. photocycloaddition
  92282. alkenes
  92283. alkyn
  92284. furans
  92285. synthesis
  92286. total
  92287. synthesis
  92288. fastigilin
  92289. furans
  92290. thiophenes
  92291. selenophenes
  92292. fused
  92293. six-membered
  92294. furazanes
  92295. furazanes
  92296. benzofurazanes
  92297. their
  92298. n-oxides
  92299. furazans
  92300. furia
  92301. furin
  92302. furin
  92303. phosphorus
  92304. containingnucleophil
  92305. reactions
  92306. furin
  92307. synthetic
  92308. aspects
  92309. fluorination
  92310. organic
  92311. furlong
  92312. furmanova
  92313. furocle
  92314. furocoumarins
  92315. furoindole
  92316. furoxans
  92317. furstner
  92318. furstner
  92319. alois
  92320. chemistry
  92321. highly
  92322. reactive
  92323. metals
  92324. furstoss
  92325. further
  92326. further
  92327. opment
  92328. ketoxime-based
  92329. pyrrole
  92330. synthesis
  92331. further
  92332. researches
  92333. furocle
  92334. rodanes
  92335. teucrium
  92336. furuhashi
  92337. furukawa
  92338. furukawa
  92339. stereoregular
  92340. sequence
  92341. regular
  92342. polymerization
  92343. furusaki
  92344. furuta
  92345. furyl
  92346. fusarium
  92347. fusco
  92348. fusco
  92349. fannicolo
  92350. cleavage
  92351. rearrangements
  92352. fused^
  92353. fused
  92354. oxacycle
  92355. synthesis
  92356. radical
  92357. cyclization
  92358. alkoxy
  92359. fused
  92360. pyrimidines
  92361. miscellaneous
  92362. systems
  92363. fused-bicyclic
  92364. fused-bicyclic
  92365. tertiary
  92366. amines
  92367. fused-ring
  92368. fused-ring
  92369. oxiranes
  92370. oxirenes
  92371. thiiranes
  92372. thiirenes
  92373. fuson
  92374. fustero
  92375. futher
  92376. futher
  92377. advances
  92378. chemistry
  92379. mannich
  92380. bases
  92381. future
  92382. fuyuhiko
  92383. cocivera
  92384. damji
  92385. stopped
  92386. fyles
  92387. fyles
  92388. biomimetic
  92389. transport
  92390. synthetic
  92391. transporte
  92392. freedman
  92393. organometall
  92394. jeffrey
  92395. sundaralingam
  92396. bibliography
  92397. crystal
  92398. mironova
  92399. kuklin
  92400. kirillova
  92401. prakash
  92402. fluor
  92403. prakash
  92404. synthesis
  92405. perfl
  92406. shvekhgeimer
  92407. zvolinskii
  92408. kobrakov
  92409. hetero
  92410. somorjai
  92411. active
  92412. sites
  92413. heterogeneous
  92414. catalysis
  92415. bennett
  92416. claisen
  92417. rearrangement
  92418. organic
  92419. synthesis
  92420. whiting
  92421. aldrichimica
  92422. guideli
  92423. bartoli
  92424. todesco
  92425. nucleophilic
  92426. substitution
  92427. linear
  92428. bianchi
  92429. micheli
  92430. gandolfi
  92431. dipolar
  92432. cycloadditi
  92433. desimoni
  92434. tacconi
  92435. heterodiene
  92436. kinetic
  92437. isotope
  92438. effects
  92439. decarboxylation
  92440. yakobson
  92441. vlasov
  92442. synthesis
  92443. recent
  92444. synthe
  92445. posner
  92446. multicomponent
  92447. annul
  92448. schmid
  92449. garratt
  92450. electrophilic
  92451. additions
  92452. carbon
  92453. henrici
  92454. olive
  92455. olive
  92456. fortschr
  92457. forsh
  92458. jaouen
  92459. lecture
  92460. effect
  92461. kunesch
  92462. poupat
  92463. biosynthetic
  92464. studies
  92465. precurs
  92466. kunesch
  92467. poupat
  92468. biosynthetic
  92469. studies
  92470. precurs
  92471. larson
  92472. organometall
  92473. silicon
  92474. silic
  92475. nelson
  92476. williams
  92477. electronic
  92478. structure
  92479. l'abbe
  92480. angew
  92481. reactions
  92482. vinyl
  92483. whitesides
  92484. angew
  92485. rockett
  92486. organometallic
  92487. maury
  92488. azaindolizine
  92489. systems
  92490. having
  92491. nitrogen
  92492. mohiuddin
  92493. reddy
  92494. ahmed
  92495. ratnam
  92496. heterocycles
  92497. aspinal
  92498. selective
  92499. degradation
  92500. carbohydrate
  92501. polyme
  92502. ohloff
  92503. singlet
  92504. oxygen
  92505. chiusoli
  92506. cassar
  92507. organic
  92508. syntheses
  92509. allylic
  92510. chiusoli
  92511. organomet
  92512. group
  92513. metal
  92514. ellis
  92515. romney
  92516. alexander
  92517. ellis
  92518. chromones
  92519. derivatives
  92520. chromenes
  92521. chromanone
  92522. pimentel
  92523. chemtech
  92524. reaction
  92525. pathways
  92526. newkome
  92527. baker
  92528. proced
  92529. newkome
  92530. baker
  92531. proced
  92532. newkome
  92533. sauer
  92534. roper
  92535. hager
  92536. construction
  92537. pettit
  92538. biosynthetic
  92539. products
  92540. cancer
  92541. chemotheraphy
  92542. lecas
  92543. nawracka
  92544. france
  92545. seyhold
  92546. flash
  92547. thermolysis
  92548. organic
  92549. compounds
  92550. stork
  92551. rychnovsky
  92552. gokel
  92553. durst
  92554. synthesis
  92555. principles
  92556. gribble
  92557. nutaitis
  92558. gribble
  92559. saulnier
  92560. heterocycles
  92561. synth
  92562. cheeseman
  92563. cookson
  92564. wiley
  92565. interscience
  92566. kabalka
  92567. aldrichimica
  92568. synthesis
  92569. kabalka
  92570. organomet
  92571. boranes
  92572. organic
  92573. kabalka
  92574. organometall
  92575. boron
  92576. boranes
  92577. kirby
  92578. electrophilic
  92579. nitroso
  92580. compounds
  92581. chemical
  92582. klumpp
  92583. examples
  92584. kramer
  92585. brown
  92586. remarkable
  92587. rearrangement
  92588. lithi
  92589. wittig
  92590. fortschr
  92591. forsch
  92592. g-alkylated
  92593. g-butyrolactones
  92594. g-hydroxy-a
  92595. g-lactams
  92596. g-lactams
  92597. cationic
  92598. cyclizations
  92599. g-lactones
  92600. g-methoxy
  92601. g-methylation
  92602. g-otbs
  92603. g-siloxy
  92604. g-substituted
  92605. gabor
  92606. gabriel
  92607. gabrielyan
  92608. gadamasetti
  92609. gaetano
  92610. gagik
  92611. gagne
  92612. gaivoronskaya
  92613. gajewski
  92614. gajewski
  92615. energy
  92616. surfaces
  92617. sigmatropic
  92618. shifts
  92619. gajewski
  92620. hydrocarbon
  92621. thermal
  92622. isomerizations
  92623. academic
  92624. gajewski
  92625. stereochemistry
  92626. thermally
  92627. induced
  92628. homolytic
  92629. gakhokidz
  92630. gakhokidz
  92631. saccharinic
  92632. acids
  92633. russian
  92634. chemical
  92635. galactomannans
  92636. galactosidic
  92637. galaev
  92638. galakhov
  92639. galambos
  92640. galan
  92641. galil
  92642. galindo
  92643. galishev
  92644. galishev
  92645. chistokletov
  92646. petrov
  92647. unsaturated
  92648. galkin
  92649. galkin
  92650. sayakhov
  92651. chaerkasov
  92652. steric
  92653. effects
  92654. gallagher
  92655. galli
  92656. galli
  92657. carlo
  92658. cesium
  92659. effect
  92660. macrocyclization
  92661. gallic
  92662. gallium
  92663. gallo
  92664. galloyl-derived
  92665. galpin
  92666. galpin
  92667. chemical
  92668. syntheses
  92669. peptides
  92670. proteins
  92671. galstyan
  92672. galwey
  92673. gamayurova
  92674. gambarotta
  92675. gambaryan
  92676. gamibaryan
  92677. gamma
  92678. gamma-alkoxybutenoli
  92679. gamma-alkylation
  92680. gamma-amino
  92681. gamma-arylation
  92682. gamma-oxygenated
  92683. gamma1
  92684. gammill
  92685. ganated
  92686. gandel'sman
  92687. gandolfi
  92688. ganem
  92689. ganem
  92690. glucose
  92691. aromatics
  92692. recent
  92693. developments
  92694. ganesh
  92695. gangliosides
  92696. gangloff
  92697. ganguly
  92698. ganic
  92699. gano-transition
  92700. ganometallic
  92701. ganosulfonium
  92702. gansow
  92703. thomas
  92704. meyers
  92705. chemistry
  92706. oxazolines
  92707. gante
  92708. gante
  92709. peptidomimetics
  92710. tailored
  92711. enzyme
  92712. inhibitors
  92713. angew
  92714. ganushchak
  92715. gaponik
  92716. garaeva
  92717. garbesi
  92718. garbesi
  92719. gottarelli
  92720. giovanni
  92721. mariani
  92722. paolo
  92723. spada
  92724. garcia
  92725. gardneria
  92726. garegg
  92727. gareth
  92728. nancy
  92729. structure
  92730. collagen
  92731. fibril
  92732. associated
  92733. garibina
  92734. garin
  92735. garlic
  92736. garnovskii
  92737. garratt
  92738. garrett
  92739. garrido
  92740. garrigues
  92741. garrou
  92742. garson
  92743. garson
  92744. staunton
  92745. methods
  92746. tracing
  92747. garst
  92748. garvey
  92749. phase
  92750. chemistry
  92751. ketenes
  92752. carbenes
  92753. acetylenes
  92754. aryne
  92755. phase
  92756. studies
  92757. negative
  92758. chemistry
  92759. silicon
  92760. gas-chromatographic
  92761. gas-chromatographic
  92762. separation
  92763. enantiomers
  92764. cyclodextri
  92765. gas-phase
  92766. gas-phase
  92767. carbanion
  92768. chemistry
  92769. gasco
  92770. gasco
  92771. boulton
  92772. furoxans
  92773. benzofuroxans
  92774. gaseous
  92775. gasic
  92776. gaspar
  92777. gaspar
  92778. silylenes
  92779. reactive
  92780. intermediates
  92781. jones
  92782. gaspar
  92783. silylenes
  92784. reactive
  92785. intermediates
  92786. jones
  92787. gasparrini
  92788. gasparrini
  92789. misiti
  92790. villani
  92791. chromatographic
  92792. optical
  92793. gassman
  92794. gasteiger
  92795. gasteiger
  92796. ihlenfeldt
  92797. collection
  92798. computer
  92799. gasteigern
  92800. gatilov
  92801. gatilov
  92802. barkhash
  92803. investigation
  92804. molecular
  92805. carboni
  92806. gattermann
  92807. gattermann-koch
  92808. gatto
  92809. gauche
  92810. gaudemer
  92811. gaudemer
  92812. relative
  92813. configurations
  92814. spectroscopy
  92815. deter
  92816. gaudino
  92817. gault
  92818. gaumont
  92819. gaumont
  92820. denis
  92821. preparation
  92822. characterization
  92823. synth
  92824. gausian
  92825. gauss
  92826. gautheron
  92827. gavezzotti
  92828. gawley
  92829. gawronski
  92830. gazizov
  92831. gazzetta
  92832. gc/ms
  92833. ge-m'-ge
  92834. gebicki
  92835. gegenion
  92836. gehlen
  92837. gehlen
  92838. marcelo
  92839. schryver
  92840. frans
  92841. resolved
  92842. fluoresce
  92843. geiger
  92844. geisberger
  92845. geissman
  92846. gel'mbol'dt
  92847. gelas
  92848. gelas
  92849. horton
  92850. acetonation
  92851. carbohydrates
  92852. under
  92853. kinetic
  92854. gelbard
  92855. gelbert
  92856. geller
  92857. geller
  92858. mechanism
  92859. elimination
  92860. ammonia
  92861. gelsemine
  92862. gelsemium
  92863. gelsimine
  92864. gem-bismetallics
  92865. gem-borazirconocene
  92866. gem-di-halocycloprop
  92867. gem-di-halocycloprop
  92868. organic
  92869. synthesis
  92870. gem-dicarboxylates
  92871. gem-dihalocyclopropa
  92872. gem-dihalocyclopropa
  92873. chemical
  92874. nthesis
  92875. gem-polyols-a
  92876. gem-polyols-a
  92877. unique
  92878. class
  92879. compound
  92880. geminal
  92881. synthesis
  92882. genealogically
  92883. genealogically
  92884. directed
  92885. synthesis
  92886. starburst/cascade
  92887. dendrime
  92888. genenal
  92889. general
  92890. general
  92891. general
  92892. catalysis
  92893. acetal
  92894. ketal
  92895. orthoester
  92896. hydrol
  92897. general
  92898. efficient
  92899. carbon
  92900. insertion
  92901. route
  92902. one-carbon-h
  92903. general
  92904. approach
  92905. synthesis
  92906. polyquinenes
  92907. general
  92908. optimisation
  92909. enantioselective
  92910. biocata
  92911. general
  92912. considerations
  92913. nomenclature
  92914. spectroscopic
  92915. identi
  92916. general
  92917. methods
  92918. nucleoside
  92919. synthesis
  92920. general
  92921. strategy
  92922. asymmetric
  92923. synthesis
  92924. picroto
  92925. atment
  92926. periselectivity
  92927. cameo
  92928. computer
  92929. program
  92930. generally
  92931. generate
  92932. generated
  92933. generating
  92934. generation
  92935. oadditions
  92936. dimethyl
  92937. bromome
  92938. generation
  92939. chemistry
  92940. allene
  92941. oxides
  92942. leading
  92943. references
  92944. generation
  92945. cyclization
  92946. unsaturated
  92947. organolithiums
  92948. generation
  92949. cycloaddition
  92950. heteroatom
  92951. substituted
  92952. generation
  92953. ion-pair
  92954. structures
  92955. unstable
  92956. carbocation
  92957. generation
  92958. reactions
  92959. novel
  92960. copper
  92961. carbenoids
  92962. generation
  92963. reactions
  92964. sp2-carbanionic
  92965. centers
  92966. generation
  92967. utilization
  92968. carbonyl
  92969. ylides
  92970. tandem
  92971. generation
  92972. isolation
  92973. characterization
  92974. arylthio
  92975. generation
  92976. lithio
  92977. trimethylsilyl
  92978. silacyclopentane
  92979. generation
  92980. substituted
  92981. ethenyl
  92982. cations
  92983. ethylened
  92984. generation
  92985. configurationally
  92986. stable
  92987. chiral
  92988. benzyllithiu
  92989. generation
  92990. allyl
  92991. lithiums
  92992. benzyl
  92993. lithiums
  92994. generation
  92995. azomethine
  92996. carbonyl
  92997. thiocarbonyl
  92998. ylides
  92999. generation
  93000. carbenes
  93001. thermal
  93002. cycloelimination
  93003. generation
  93004. cation
  93005. radicals
  93006. allylic
  93007. sulfides
  93008. generation
  93009. enantiomerically
  93010. enriched
  93011. lithium
  93012. indenides
  93013. generation
  93014. oxiranyl
  93015. lithium
  93016. compounds
  93017. stannyl
  93018. epoxid
  93019. generation
  93020. radicals
  93021. generation
  93022. simple
  93023. enols
  93024. solution
  93025. generation
  93026. sulfinyl
  93027. carbenoid
  93028. chloro
  93029. sulfoxi
  93030. generation
  93031. synthetic
  93032. 12-vinyl
  93033. rearrangements
  93034. generation
  93035. thermochemistry
  93036. chemistry
  93037. carbene
  93038. anion
  93039. generations
  93040. genetic
  93041. genetic
  93042. engineering
  93043. hybrid
  93044. antibiotics
  93045. progress
  93046. report
  93047. genetically
  93048. genevieve
  93049. genicot
  93050. genius
  93051. gennady
  93052. genokhova
  93053. genokhova
  93054. melent'eva
  93055. berezovskii
  93056. synthesis
  93057. gensler
  93058. genus
  93059. geochemical
  93060. geoffrey
  93061. geoffroy
  93062. geoffroy
  93063. wrighton
  93064. organometallic
  93065. photochemistry
  93066. geohopanoids
  93067. geometric
  93068. geometric
  93069. topological
  93070. thinking
  93071. organic
  93072. chemistry
  93073. geometric
  93074. requirements
  93075. proton
  93076. transfers
  93077. geometrical
  93078. geometrical
  93079. isomerization
  93080. carotenoids
  93081. dichloromethane
  93082. geometries
  93083. geometry
  93084. geometry
  93085. conformational
  93086. properties
  93087. geometry
  93088. carbanionic
  93089. moiety
  93090. infuences
  93091. diastereoselectivit
  93092. georg
  93093. georg
  93094. gunda
  93095. organic
  93096. chemistry
  93097. lactams
  93098. george
  93099. george
  93100. george
  93101. photooxygenations
  93102. nitrogen
  93103. heterocycles
  93104. george
  93105. mitra
  93106. sukumaran
  93107. thermal
  93108. photochemical
  93109. georges
  93110. georghiou
  93111. georgia
  93112. georgio
  93113. gerald
  93114. geraniol
  93115. gerard
  93116. gerardo
  93117. gerasimov
  93118. gerasimov
  93119. parmon
  93120. photocatalysis
  93121. transition
  93122. metal
  93123. gerasimova
  93124. gerasimova
  93125. kolchina
  93126. smiles
  93127. rearrangement
  93128. gerhard
  93129. gerlach
  93130. german
  93131. germanium
  93132. germanium-germanium
  93133. germanyR
  93134. germyl
  93135. germylenes
  93136. germylenes
  93137. stannylenes
  93138. gernot
  93139. gerratt
  93140. gerson
  93141. gerson
  93142. fabian
  93143. applications
  93144. endor
  93145. spectroscopy
  93146. radical
  93147. gerst
  93148. geruchsinn
  93149. gerus
  93150. gerwick
  93151. gerwick
  93152. william
  93153. nagle
  93154. proteau
  93155. philip
  93156. oxylipins
  93157. gerzon
  93158. gesser
  93159. getchell
  93160. geterotsikl
  93161. getting
  93162. gevaza
  93163. gevorgyan
  93164. gharbia
  93165. gheorghiu
  93166. ghoneim
  93167. ghoneim
  93168. nagwa
  93169. suppan
  93170. solvation
  93171. states
  93172. solven
  93173. ghosez
  93174. ghosez
  93175. genicot
  93176. christophe
  93177. gouverneur
  93178. veronique
  93179. chiral
  93180. ghosh
  93181. ghosh
  93182. tirthankar
  93183. reaction
  93184. carbenes
  93185. divalent
  93186. sulfur
  93187. giacomini
  93188. giambattista
  93189. giancola
  93190. gianfranco
  93191. gianluca
  93192. giannis
  93193. giannis
  93194. anthanassios
  93195. kolter
  93196. thomas
  93197. peptido
  93198. mimetics
  93199. giannis
  93200. athanassios
  93201. sialyl
  93202. lewis
  93203. group
  93204. analogs
  93205. giant
  93206. gibberellic
  93207. gibberellin
  93208. gibberellins
  93209. gibberlic
  93210. gibson
  93211. gibson
  93212. prostaglandins
  93213. thromboxanes
  93214. biosynthetic
  93215. gibson
  93216. ligands
  93217. compass
  93218. needles
  93219. orientations
  93220. gidaspov
  93221. gieiter
  93222. gieiter
  93223. spanget
  93224. larsen
  93225. aspects
  93226. photoelect
  93227. gielen
  93228. giese
  93229. giguere
  93230. gilbert
  93231. gilbert
  93232. andrew
  93233. baggott
  93234. essentials
  93235. molecular
  93236. photochem
  93237. gilchrist
  93238. gilchrist
  93239. heterocyclic
  93240. chemistry
  93241. wiley
  93242. essex
  93243. gilchrist
  93244. thomas
  93245. synthesis
  93246. membered
  93247. aromatic
  93248. heter
  93249. gilday
  93250. gilge
  93251. gilge
  93252. roesky
  93253. herbert
  93254. structurally
  93255. characterized
  93256. gilgen
  93257. pigments
  93258. fungi
  93259. macromycetes
  93260. natural
  93261. product
  93262. report
  93263. gillespie
  93264. gillespie
  93265. cluster
  93266. compounds
  93267. gillian
  93268. gilligan
  93269. gilman
  93270. gilvocarcins
  93271. gilyarov
  93272. gilyarov
  93273. imide
  93274. amine
  93275. imide
  93276. imide
  93277. rearrangements
  93278. ginak
  93279. gineityte
  93280. gingrich
  93281. gingrich
  93282. mesoionic
  93283. oxazoles
  93284. oxazoles
  93285. gingrich
  93286. henry
  93287. ghosh
  93288. tirthankar
  93289. huang
  93290. qiurong
  93291. jones
  93292. ginkgolide
  93293. ginos
  93294. ginsburg
  93295. ginzburg
  93296. ginzburg
  93297. chemistry
  93298. cymantrene
  93299. russian
  93300. chemical
  93301. giolitti
  93302. giordano
  93303. giorgio
  93304. giovanni
  93305. giralt
  93306. girard
  93307. girolamo
  93308. gilchrist
  93309. thomas
  93310. synthesis
  93311. membered
  93312. aromatic
  93313. heter@
  93314. girolamo
  93315. gleiter
  93316. photoelectron
  93317. spectra
  93318. bonding
  93319. small
  93320. glycals
  93321. enantiospecific
  93322. synthesis@
  93323. glycopyranosides@
  93324. glycosylation
  93325. silylated
  93326. eterocyclic
  93327. bases@
  93328. ystematic@
  93329. golankiewicz@
  93330. gololobov
  93331. balitsky
  93332. aminocarbonyl
  93333. related@
  93334. gordon
  93335. francisco
  93336. schlegel
  93337. theoretical
  93338. investigat@
  93339. gottlieb
  93340. flavonoids
  93341. indispensable
  93342. additions
  93343. harry
  93344. range
  93345. electron
  93346. transfer
  93347. proteins
  93348. greenhill
  93349. grayshan
  93350. cevane
  93351. group
  93352. veratrum
  93353. grethe
  93354. griffiths
  93355. william
  93356. ruthenium
  93357. complexes
  93358. organic
  93359. oxida@
  93360. grimmett
  93361. advances
  93362. imidazole
  93363. chemistry
  93364. groove
  93365. group
  93366. group
  93367. transfer
  93368. addition
  93369. reactions
  93370. methyl
  93371. phenylseleno
  93372. groups
  93373. gschwend
  93374. rodriguez
  93375. heteroatom
  93376. facilitated
  93377. lithiation@
  93378. guidelines@
  93379. girolamo
  93380. girreser
  93381. girreser
  93382. ulrich
  93383. giuffrida
  93384. daniele
  93385. kohnke
  93386. franz
  93387. mathias
  93388. gisele
  93389. gitis
  93390. gitis
  93391. kaminskii
  93392. janovsky
  93393. sigma
  93394. complexes
  93395. gitto
  93396. giucosidase
  93397. giudici
  93398. giuffrida
  93399. giulia
  93400. giuliana
  93401. giumanini
  93402. giuseppe
  93403. giuseppina
  93404. giutamyl
  93405. given
  93406. givens
  93407. givens
  93408. photoextrusion
  93409. small
  93410. molecules
  93411. organic
  93412. givens
  93413. richard
  93414. kueper
  93415. william
  93416. photochemistry
  93417. giving
  93418. gladfelter
  93419. gladfelter
  93420. geoffroy
  93421. mixed
  93422. metal
  93423. clusters
  93424. gladiali
  93425. gladysz
  93426. gladysz
  93427. trialkylborohydrides
  93428. organometallic
  93429. synthesis
  93430. glaenzer
  93431. glands
  93432. glanzer
  93433. glasfeld
  93434. glasgow
  93435. glass
  93436. glebov
  93437. glebova
  93438. gleiter
  93439. gleiter
  93440. photoelectron
  93441. spectra
  93442. bonding
  93443. small
  93444. gleiter
  93445. cycloalkadiynes
  93446. triple
  93447. bonds
  93448. strai
  93449. gleiter
  93450. kratz
  93451. detlef
  93452. superphanes
  93453. accounts
  93454. chemical
  93455. glenn
  93456. glese
  93457. glinka
  93458. glochidicine
  93459. glochidine
  93460. gloria
  93461. glormani
  93462. glossary
  93463. glossary
  93464. terms
  93465. physical
  93466. organic
  93467. chemistry
  93468. glotter
  93469. glotter
  93470. withanolides
  93471. related
  93472. ergostane
  93473. steroids
  93474. glotter
  93475. withanolides
  93476. related
  93477. ergostane
  93478. steroids
  93479. glover
  93480. glucals
  93481. glucosaccharino
  93482. glucosaccharino-lact
  93483. glucose
  93484. glucosidase
  93485. glucosinolates
  93486. glucuronide
  93487. glukhovtsevO
  93488. glushkov
  93489. glutaconaldehyde
  93490. glutamate
  93491. glutaraldehyde
  93492. glutarates
  93493. glutathione
  93494. glycal
  93495. glycal-aglycon
  93496. glycals
  93497. glycals
  93498. enantiospecific
  93499. synthesis
  93500. glycals
  93501. palladium-mediated
  93502. c-glycosyl
  93503. formation
  93504. glycans
  93505. glycer
  93506. glyceraldehyde
  93507. glycerol
  93508. glycerophosphatides
  93509. glycidic
  93510. glycidol
  93511. glycidyl
  93512. glycinamide
  93513. glycinamides
  93514. glycine
  93515. glycinoeclepin
  93516. glycinoelepin
  93517. glyco
  93518. glycoconjugate
  93519. glycoconjugates
  93520. glycol
  93521. glycol-cleavage
  93522. glycol-cleavage
  93523. reactions
  93524. glycolate
  93525. glycolic
  93526. glycolipids
  93527. glycolipids
  93528. immunomodulators
  93529. synthesis
  93530. properties
  93531. glycolipids
  93532. immunomodulators-syn
  93533. properties
  93534. glycolipoids
  93535. glycolization
  93536. glycols
  93537. glycoorganic
  93538. glycopeptides
  93539. glycopeptides
  93540. biological
  93541. interest
  93542. challenge
  93543. chemica
  93544. glycoprocessing
  93545. glycoprotein
  93546. glycoproteins
  93547. glycopyranosides
  93548. glycosidase
  93549. glycosidases
  93550. glycosidation
  93551. glycosidation
  93552. sialic
  93553. glycoside
  93554. glycosidesX
  93555. glycosidic
  93556. glycosiduronic
  93557. glycosphingolipids
  93558. glycosyl
  93559. glycosyl
  93560. seleno
  93561. tellurophosphates
  93562. glycosylated
  93563. glycosylation
  93564. glycosylation
  93565. 22'-indolylindolines
  93566. glycosylation
  93567. merrifield
  93568. resin
  93569. using
  93570. anomeric
  93571. sulfoxi
  93572. glycosylations
  93573. glycosylmanganese
  93574. glycosylmanganese
  93575. pentacarbonyl
  93576. complexes
  93577. organomanganese
  93578. glyoxal
  93579. glyzin
  93580. gnewuch
  93581. sterols
  93582. marine
  93583. invertebrates
  93584. composition
  93585. gobel
  93586. godleski
  93587. godleski
  93588. schleyer
  93589. osawa
  93590. wipke
  93591. systematic
  93592. godovikov
  93593. godovikova
  93594. goeddel
  93595. goeffrey
  93596. goerge
  93597. goergens
  93598. goetz
  93599. goffredo
  93600. gogte
  93601. gogte
  93602. modak
  93603. thiiranium
  93604. salts/ions
  93605. reaction
  93606. interm
  93607. gokel
  93608. gokel
  93609. ecbegoyen
  93610. lariat
  93611. ethers
  93612. membranes
  93613. gokel
  93614. weber
  93615. phase
  93616. transfer
  93617. catalysis
  93618. general
  93619. princip
  93620. gokel
  93621. george
  93622. crown
  93623. ethers
  93624. cryptands
  93625. royal
  93626. society
  93627. gokel
  93628. george
  93629. lariat
  93630. ethers
  93631. simple
  93632. sidearms
  93633. supramo
  93634. gokel
  93635. george
  93636. medina
  93637. julio
  93638. chensheng
  93639. property
  93640. directed
  93641. gol'dberg
  93642. gol'dfarb
  93643. gol'ding
  93644. gol'dshleger
  93645. gol'dshleger
  93646. moravskii
  93647. reactions
  93648. hydrocarbons
  93649. golankiewicz
  93650. mcadam
  93651. radiation
  93652. lnduced
  93653. organic
  93654. hydrogen
  93655. isotope
  93656. gold's
  93657. goldberg
  93658. goldberg
  93659. phase
  93660. transfer
  93661. catalysis
  93662. selected
  93663. problems
  93664. golden
  93665. golding
  93666. goldmann
  93667. goldmann
  93668. siegfried
  93669. stoltefuss
  93670. jurgen
  93671. dihydropyridines
  93672. goldschmidt
  93673. goldstein
  93674. goldstein
  93675. hayes
  93676. lectins
  93677. carbohydrate
  93678. binding
  93679. goldstein
  93680. organic
  93681. chemicals
  93682. biomass
  93683. press
  93684. golebiewski
  93685. golebiewski
  93686. wrobel
  93687. lythraceae
  93688. alkaloids
  93689. golebiowski
  93690. golebiowski
  93691. jurczak
  93692. janusz
  93693. amino
  93694. hydroxy
  93695. acids
  93696. golfier
  93697. golfier
  93698. determination
  93699. configurations
  93700. infrared
  93701. spectr
  93702. golod
  93703. gololobov
  93704. gololobov
  93705. kasukhin
  93706. recent
  93707. advances
  93708. staudinge
  93709. gololobov
  93710. zhmurova
  93711. kasukhin
  93712. sixty
  93713. years
  93714. gololobov
  93715. balitsky
  93716. aminocarbonyl
  93717. related
  93718. golovin
  93719. golovina
  93720. golubev
  93721. golubev
  93722. kolomiets
  93723. fokin
  93724. reactions
  93725. polyfluoro
  93726. gomez
  93727. gomez
  93728. puyoug
  93729. armando
  93730. darszon
  93731. alberto
  93732. tuena
  93733. gomez
  93734. puyoug
  93735. gomisin
  93736. goniofufurone
  93737. gonzalez
  93738. excellent
  93739. diastereoselectiviti
  93740. asymmetric
  93741. radical
  93742. goodall
  93743. goodfellow
  93744. goodin
  93745. goodman
  93746. goodman
  93747. chorev
  93748. linear
  93749. modified
  93750. retro
  93751. peptide
  93752. structures
  93753. goodson
  93754. gopalakrishna
  93755. goraeva
  93756. gorbatenko
  93757. gorbatenko
  93758. samarai
  93759. synthesis
  93760. reactions
  93761. alpha
  93762. gorbatenko
  93763. victor
  93764. chemistry
  93765. chlorocarbonyl
  93766. isocyanate
  93767. gorbovoi
  93768. gordeev
  93769. gordon
  93770. gordon
  93771. francisco
  93772. schlegel
  93773. theoretical
  93774. investigat
  93775. gorelik
  93776. gorenstein
  93777. gorenstein
  93778. conformation
  93779. dynamics
  93780. protein
  93781. gorewitt
  93782. gorewitt
  93783. tsutsui
  93784. sigma
  93785. rearrangements
  93786. their
  93787. gorgiacerone
  93788. gorin
  93789. gorin
  93790. carbon
  93791. nuclear
  93792. magnetic
  93793. resonance
  93794. spectroscop
  93795. gorman
  93796. gosisin
  93797. gosney
  93798. gosney
  93799. rowley
  93800. transformations
  93801. phosphorus
  93802. stabilize
  93803. goswami
  93804. goswami
  93805. shyamaprosad
  93806. molybdenum
  93807. cofactor
  93808. biological
  93809. gothe
  93810. fumitaka
  93811. ogawa
  93812. tomoya
  93813. recent
  93814. aspects
  93815. glycoconjugate
  93816. goton
  93817. gottarelli
  93818. gottfried
  93819. gottlieb
  93820. gottlieb
  93821. techniques
  93822. signal
  93823. assignment
  93824. gottlieb
  93825. neolignans
  93826. progress
  93827. chemistry
  93828. gottlieb
  93829. flavonoids
  93830. indispensable
  93831. additions
  93832. goulaouic
  93833. gould
  93834. goumont
  93835. goups
  93836. gouverneur
  93837. govindachan
  93838. govindachari
  93839. govundachari
  93840. gozyo
  93841. gpectroscopy
  93842. graboski
  93843. grabowski
  93844. grabowski
  93845. zbigniew
  93846. electron
  93847. transfer
  93848. flexible
  93849. molecules
  93850. gracilins
  93851. graczyk
  93852. graczyk
  93853. piotr
  93854. mikolajczyk
  93855. marian
  93856. anomeric
  93857. effect
  93858. origin
  93859. grade
  93860. graft
  93861. gragerov
  93862. graham
  93863. grajkowski
  93864. gramineae
  93865. grandberg
  93866. grandbois
  93867. grandfather
  93868. grandirubrine
  93869. granditropone
  93870. grant
  93871. grant
  93872. david
  93873. higuchi
  93874. takeru
  93875. solubility
  93876. behavior
  93877. organi
  93878. graph
  93879. graphicQ
  93880. graphics
  93881. graphite
  93882. grapov
  93883. grapov
  93884. razvodovskayn
  93885. mel'nikov
  93886. diazadiphosphetid
  93887. graselli
  93888. grasselli
  93889. grasso
  93890. gratzel
  93891. harry
  93892. range
  93893. electron
  93894. transfer
  93895. proteins
  93896. grayshan
  93897. grayson
  93898. grayson
  93899. monoterpenoids
  93900. natural
  93901. product
  93902. grazia
  93903. graziani
  93904. great
  93905. greater
  93906. grebenik
  93907. grebenkina
  93908. greef
  93909. green
  93910. green
  93911. lahav
  93912. rabinovich
  93913. asymmetric
  93914. synthesis
  93915. green
  93916. stereochemical
  93917. bridge
  93918. between
  93919. spectrometry
  93920. green
  93921. malcolm
  93922. mountford
  93923. philip
  93924. cyclopentadienyl
  93925. molybden
  93926. greenberg
  93927. greenberg
  93928. liebman
  93929. strained
  93930. organic
  93931. molecules
  93932. academic
  93933. greenberg
  93934. arthur
  93935. guanli
  93936. structural
  93937. relationships
  93938. silat
  93939. greene
  93940. greene
  93941. protective
  93942. groups
  93943. organic
  93944. synthesis
  93945. wiley
  93946. greene
  93947. theodora
  93948. peter
  93949. protective
  93950. groups
  93951. organi
  93952. greenhill
  93953. greenhill
  93954. grayshan
  93955. cevane
  93956. group
  93957. veratrum
  93958. greenwich
  93959. greenwood
  93960. gregory
  93961. grehn
  93962. greiciute
  93963. grekov
  93964. grekov
  93965. veselov
  93966. alpha
  93967. effect
  93968. chemistry
  93969. grellmann
  93970. grendze
  93971. grethe
  93972. grethe
  93973. grethe
  93974. isoquinolines
  93975. chemistry
  93976. heterocyclic
  93977. compound
  93978. grety
  93979. greuter
  93980. roger
  93981. structure
  93982. bonding
  93983. parent
  93984. hydrides
  93985. grevels
  93986. gribblec
  93987. gribble
  93988. natural
  93989. products
  93990. containing
  93991. cyclohexane
  93992. cyclo
  93993. gribble
  93994. gordon
  93995. approaches
  93996. synthesis
  93997. antitumo
  93998. gribble
  93999. gordon
  94000. recent
  94001. developments
  94002. indole
  94003. synthesi
  94004. grieco
  94005. grieco
  94006. organic
  94007. chemistry
  94008. unconventional
  94009. solvents
  94010. griengl
  94011. grierson
  94012. griesbeck
  94013. griesbeck
  94014. mauder
  94015. harald
  94016. stadtmueller
  94017. stefan
  94018. intersyst
  94019. grieve
  94020. grif3lths
  94021. griffin
  94022. griffithv
  94023. griffiths
  94024. griffiths
  94025. colour
  94026. constitution
  94027. organic
  94028. molecules
  94029. griffiths
  94030. marcos
  94031. perrio
  94032. saberi
  94033. thomas
  94034. griffiths
  94035. william
  94036. ruthenium
  94037. complexes
  94038. organic
  94039. oxida
  94040. grigg
  94041. grighchuk
  94042. grighchuk
  94043. gorbovoi
  94044. ganushchak
  94045. dombrovskii
  94046. grignard
  94047. grignard
  94048. organolithium
  94049. reagents
  94050. derived
  94051. grignard
  94052. reactions
  94053. non-metallic
  94054. substances
  94055. grignard
  94056. reagent
  94057. formation
  94058. freely
  94059. diffusing
  94060. radica
  94061. inter
  94062. grignard
  94063. reagents
  94064. chemically
  94065. activated
  94066. magnesium
  94067. grigor'eva
  94068. grigor'eva
  94069. pinsker
  94070. methods
  94071. synthesis
  94072. griller
  94073. griller
  94074. ingold
  94075. electron
  94076. paramagnetic
  94077. resonance
  94078. grimes
  94079. grimes
  94080. russell
  94081. boron
  94082. carbon
  94083. ligands
  94084. organometallic
  94085. grimmett
  94086. grimmett
  94087. advances
  94088. imidazole
  94089. chemistry
  94090. grimmett
  94091. iddon
  94092. synthesis
  94093. reactions
  94094. lithiated
  94095. grimmett
  94096. halogenation
  94097. heterocycles
  94098. grimmett
  94099. halogenation
  94100. heterocycles
  94101. heterocycle
  94102. grimshaw
  94103. grimshaw
  94104. silva
  94105. photochemistry
  94106. photocyclization
  94107. grinberg
  94108. grinter
  94109. grisebach
  94110. grisebach
  94111. biosynthesis
  94112. sugar
  94113. components
  94114. antibiotic
  94115. grisebach
  94116. phytoalexins
  94117. chemical
  94118. defense
  94119. substances
  94120. grisenti
  94121. groen
  94122. groenen
  94123. groenen
  94124. polyenals
  94125. retinal
  94126. elect
  94127. gromov
  94128. gromov
  94129. sergei
  94130. aleksei
  94131. enamine
  94132. rearrangement
  94133. heteroc
  94134. groneberg
  94135. gronowitz
  94136. gronowitz
  94137. thiophene
  94138. derivatives
  94139. chemist
  94140. gronowitz
  94141. thiophene
  94142. derivatives
  94143. chemist
  94144. groot
  94145. groove
  94146. groove
  94147. groove-binding
  94148. boureier
  94149. absolute
  94150. configurations
  94151. select
  94152. gross
  94153. gross
  94154. phytoalexine
  94155. related
  94156. plant
  94157. substances
  94158. gross
  94159. meienhofer
  94160. peptide
  94161. peptides
  94162. grotjahn
  94163. grotjahn
  94164. carbene
  94165. complexes
  94166. chromium
  94167. bearing
  94168. ground
  94169. group
  94170. group
  94171. group
  94172. metalloles
  94173. synthesis
  94174. organic
  94175. chemistry
  94176. physic
  94177. group
  94178. metal
  94179. catalyzed
  94180. aminolysis
  94181. oxazolidinon
  94182. group
  94183. transfer
  94184. addition
  94185. reactions
  94186. methyl
  94187. phenylseleno
  94188. group
  94189. transfer
  94190. addition
  94191. reactions
  94192. selenomalonitriles
  94193. group
  94194. metal-catalysed
  94195. forming
  94196. sequences
  94197. group
  94198. transition
  94199. metals
  94200. organic
  94201. synthesis
  94202. group-4
  94203. group-8
  94204. grouping
  94205. groups
  94206. groups
  94207. groutas
  94208. groutas
  94209. felker
  94210. synthetic
  94211. applications
  94212. cyanotrimethy
  94213. grove
  94214. grove
  94215. macrocyclic
  94216. trichothecenes
  94217. natural
  94218. product
  94219. reports
  94220. grovenstein
  94221. grovenstein
  94222. skeletal
  94223. rearrangements
  94224. organoalkali
  94225. groves
  94226. growth
  94227. growth-inhibiting
  94228. grubbs
  94229. gruber
  94230. grubler
  94231. gruenanger
  94232. grundon
  94233. grundon
  94234. quinoline
  94235. alkaloids
  94236. related
  94237. anthranilic
  94238. grundon
  94239. biosynthesis
  94240. aromatic
  94241. hemiterpenes
  94242. grunwald
  94243. grushin
  94244. grushin
  94245. vladimir
  94246. alper
  94247. howard
  94248. transformations
  94249. chloroare
  94250. grushin
  94251. vladimir
  94252. reductive
  94253. elimination
  94254. hydrogen
  94255. chlorid
  94256. gryaznov
  94257. grynkiewicz
  94258. gschwend
  94259. gschwend
  94260. rodriguez
  94261. heteroatom
  94262. facilitated
  94263. lithiation
  94264. guangyi
  94265. guanidine
  94266. guanidines
  94267. guanidino
  94268. guanine
  94269. guanines
  94270. guanli
  94271. guanti
  94272. guarna
  94273. guarnieri
  94274. guattetia
  94275. gubnitskaya
  94276. gubnitskaya
  94277. peresypkina
  94278. samarai
  94279. aminophosph
  94280. gudat
  94281. guedjp
  94282. guenard
  94283. guenard
  94284. daniel
  94285. gueritte
  94286. voegelein
  94287. francoise
  94288. potier
  94289. pierre
  94290. guengerich
  94291. guengerich
  94292. peter
  94293. macdonald
  94294. timothy
  94295. sequential
  94296. electron
  94297. guenin
  94298. guenter
  94299. guenther
  94300. guerin
  94301. gueritte
  94302. guerriero
  94303. guerriero
  94304. paolo
  94305. vigato
  94306. pietro
  94307. alessandro
  94308. fenton
  94309. david
  94310. guest
  94311. guests
  94312. guette
  94313. guggisberg
  94314. guggultetrols
  94315. guida
  94316. guideL
  94317. guidebook
  94318. guidelines
  94319. guides
  94320. guidi
  94321. guidi
  94322. canfarini
  94323. giolitti
  94324. pasqui
  94325. pestellini
  94326. arcamon
  94327. guido
  94328. guiilet
  94329. guilford
  94330. guillanton
  94331. guilloton
  94332. guinaudeau
  94333. guindi
  94334. guindon
  94335. guingant
  94336. guinn
  94337. guiseppe
  94338. gukasyan
  94339. gukasyan
  94340. galstyan
  94341. avetisyan
  94342. synthesis
  94343. structure
  94344. gul'yanova
  94345. gulik
  94346. gulono
  94347. gulopyranose
  94348. gunaratne
  94349. gunawardana
  94350. gunda
  94351. gundula
  94352. gunsteren
  94353. gunter
  94354. gunther
  94355. gupta
  94356. gupta
  94357. ashok
  94358. xiaoyong
  94359. snyder
  94360. james
  94361. james
  94362. genera
  94363. gupta
  94364. quantitative
  94365. structure
  94366. activity
  94367. relationship
  94368. studi
  94369. gupton
  94370. gurjar
  94371. gurnos
  94372. gusar
  94373. gusar
  94374. synthesis
  94375. heterocycles
  94376. wittig
  94377. reacti
  94378. gusarova
  94379. gusarova
  94380. tatarinova
  94381. sinegovskaya
  94382. vinyl
  94383. telluride
  94384. gusel'nikov
  94385. guseva
  94386. guseva
  94387. gushurst
  94388. gussier
  94389. gustav
  94390. gustavo
  94391. gustorf
  94392. gustowski
  94393. guther
  94394. gutherie
  94395. gutherie
  94396. electron
  94397. transfer
  94398. reactions
  94399. carbanions
  94400. guthrie
  94401. gutman
  94402. gutman
  94403. nucleophilic
  94404. aromatic
  94405. displacement
  94406. influe
  94407. gutsche
  94408. guziec
  94409. gylcal
  94410. gylcosidase
  94411. gylcosides
  94412. gyorgy
  94413. gypsetin
  94414. guseva
  94415. molecular
  94416. states
  94417. molecular
  94418. orbitals
  94419. tetrahedron
  94420. degenerate
  94421. gunther
  94422. jikeli
  94423. spectra
  94424. cyclic
  94425. monoenes
  94426. hydroc@
  94427. vyplel
  94428. chimia
  94429. preparative
  94430. fluorinations
  94431. haddadin
  94432. isobenzofuran
  94433. heterocycles
  94434. review@
  94435. halevi@
  94436. halket@
  94437. phosphorus
  94438. stereochemistry
  94439. mechanistic
  94440. halogenoalkyl
  94441. complexes
  94442. transition
  94443. metals@
  94444. hamada
  94445. hanessian
  94446. approaches
  94447. total
  94448. synthesis
  94449. natural
  94450. hanson
  94451. diterpenoids
  94452. natural
  94453. harborne
  94454. advances
  94455. chemical
  94456. ecology
  94457. natural
  94458. product
  94459. haslam
  94460. plant
  94461. polyphenols
  94462. vegetable
  94463. tannins
  94464. gallic
  94465. hauser@
  94466. heaney
  94467. harry
  94468. novel
  94469. organic
  94470. peroxygen
  94471. reagents
  94472. sulfur
  94473. bonding
  94474. organic
  94475. chemistry
  94476. sulfur
  94477. alper
  94478. organomet
  94479. homogeneous
  94480. phase
  94481. alper
  94482. organic
  94483. syntheses
  94484. pentacarbonyl
  94485. organi
  94486. kagan
  94487. tetrahedron
  94488. lanthanides
  94489. kagan
  94490. asymmetric
  94491. catalysi
  94492. molecular
  94493. states
  94494. molecular
  94495. orbitals
  94496. bonnemann
  94497. brijoux
  94498. bonnemann
  94499. angew
  94500. organocobalt
  94501. brunner
  94502. organomet
  94503. enantioselective
  94504. brown
  94505. singaram
  94506. chemtech
  94507. asymmetric
  94508. brown
  94509. borabicyclo
  94510. 3.3.1
  94511. nonane
  94512. brown
  94513. negishi
  94514. boraheterocycles
  94515. cyclic
  94516. hydrobor
  94517. brown
  94518. israel
  94519. borane
  94520. adventure
  94521. brown
  94522. organometal
  94523. footsteps
  94524. brown
  94525. organoboranes
  94526. brown
  94527. plenary
  94528. lecture
  94529. organ
  94530. brown
  94531. krishnamurthy
  94532. brown
  94533. classical
  94534. problem
  94535. plenum
  94536. review
  94537. hansen
  94538. senning
  94539. reacti
  94540. ottenheijm
  94541. herscheid
  94542. tetrahedron
  94543. degenerate
  94544. gesser
  94545. hunter
  94546. prakash
  94547. hartzler
  94548. aromatic
  94549. aldehyde
  94550. leuco
  94551. photoxidation
  94552. jakubke
  94553. konnecke
  94554. angew
  94555. niall
  94556. microsequence
  94557. analysis
  94558. biologically
  94559. active
  94560. chemically
  94561. induced
  94562. nuclear
  94563. polarization
  94564. tetrahedron
  94565. symposia
  94566. print
  94567. struc
  94568. zimmerman
  94569. recent
  94570. mechanistic
  94571. exploratory
  94572. organic
  94573. zimmerman
  94574. mobius
  94575. huckel
  94576. treatment
  94577. organic
  94578. systems
  94579. felkin
  94580. swierczewski
  94581. tetrahedron
  94582. activat
  94583. firouzabadi
  94584. iranpoor
  94585. kiaeezadeh
  94586. toofan
  94587. tetrahedr
  94588. forster
  94589. vogtle
  94590. steric
  94591. interactions
  94592. organic
  94593. chemis
  94594. aurich
  94595. weiss
  94596. fortschritte
  94597. forschung
  94598. viehe
  94599. captodative
  94600. viehe
  94601. heterocyclizations
  94602. iminium
  94603. synthons
  94604. gunther
  94605. jikeli
  94606. spectra
  94607. cyclic
  94608. monoenes
  94609. hydroc
  94610. mantsch
  94611. saito
  94612. smith
  94613. deuterium
  94614. magnetic
  94615. reson
  94616. wasserman
  94617. mccarthy
  94618. prowse
  94619. hagemann
  94620. synthesis
  94621. reactions
  94622. chloro
  94623. carbonyl
  94624. bashir
  94625. hashemi
  94626. meador
  94627. tetrahedron
  94628. higuchi
  94629. kobayashi
  94630. sakata
  94631. misumi
  94632. tetrahedron
  94633. bestmann
  94634. phosphacumulene
  94635. ylids
  94636. phosphaallene
  94637. ylids
  94638. schneider
  94639. sangwan
  94640. angew
  94641. kwart
  94642. orbitals
  94643. chemistry
  94644. silicon
  94645. blewitt
  94646. indolizine
  94647. derivatives
  94648. additional
  94649. hoffman
  94650. angew
  94651. hoffmann
  94652. angew
  94653. meier
  94654. zeller
  94655. thermal
  94656. photochemical
  94657. cycloelimin
  94658. meier
  94659. tetrahedron
  94660. strained
  94661. cycloalkenyn
  94662. millauer
  94663. schwertfeger
  94664. siegemund
  94665. angew
  94666. huisman
  94667. syntheses
  94668. functionalized
  94669. isoprene
  94670. building
  94671. paulsen
  94672. synthesis
  94673. amino
  94674. branched
  94675. oligosacc
  94676. pfander
  94677. advances
  94678. synthes
  94679. pines
  94680. stalick
  94681. catalyzed
  94682. reactions
  94683. hydrocar
  94684. pommer
  94685. nurrenbach
  94686. pommer
  94687. wittig
  94688. reaetion
  94689. industrial
  94690. praetice
  94691. prinzbach
  94692. knothe
  94693. multi
  94694. seikaly
  94695. tidwell
  94696. tetrahedron
  94697. additio
  94698. simon
  94699. angew
  94700. chiral
  94701. stetter
  94702. angew
  94703. catalyzed
  94704. additions
  94705. stetter
  94706. angew
  94707. catalyzed
  94708. additi
  94709. suschitzky
  94710. croat
  94711. benzimidazoles
  94712. suzuki
  94713. reactions
  94714. aromatic
  94715. nitration
  94716. synthetic
  94717. tominaga
  94718. seventh
  94719. international
  94720. vyplel
  94721. chimia
  94722. preparative
  94723. fluorinations
  94724. moore
  94725. decker
  94726. conjugated
  94727. werner
  94728. varieties
  94729. sandwich
  94730. compounds
  94731. angew
  94732. yasuda
  94733. tatsumi
  94734. nakamura
  94735. zahner
  94736. aspects
  94737. antibiotic
  94738. research
  94739. angewand
  94740. h-bond
  94741. h-cyclopentadienyl
  94742. h-organometal
  94743. h-pyrrole
  94744. h4-diene
  94745. h6-arene-h5-cyclopen
  94746. h6-arene-h5-cyclopen
  94747. ruthenium
  94748. complexes
  94749. related
  94750. systems
  94751. haack
  94752. haaksma
  94753. haaland
  94754. alois
  94755. periodic
  94756. system
  94757. functional
  94758. groups
  94759. formalism
  94760. habich
  94761. habich
  94762. effenberger
  94763. preparation
  94764. heteroaryltri
  94765. hacksell
  94766. haddad
  94767. haddadin
  94768. haddadin
  94769. isobenzofuran
  94770. heterocycles
  94771. review
  94772. haddadin
  94773. makhluf
  94774. issidorides
  94775. costas
  94776. beirut
  94777. reaction
  94778. hadjiarapoglou
  94779. hadjipavlou
  94780. hadjipavlou
  94781. litina
  94782. hansch
  94783. quantitative
  94784. structure
  94785. activit
  94786. hafez
  94787. hafner
  94788. hafnium
  94789. hagaman
  94790. hagan
  94791. hagemann
  94792. hager
  94793. hahnfeld
  94794. haider
  94795. haider
  94796. norbert
  94797. heinisch
  94798. gottfried
  94799. recent
  94800. advances
  94801. haiduc
  94802. haiduc
  94803. newton
  94804. stereochemical
  94805. aspects
  94806. tellu
  94807. haifang
  94808. haines
  94809. haire
  94810. hajos
  94811. hajos
  94812. aldol
  94813. related
  94814. reactions
  94815. carbon
  94816. carbon
  94817. hakan
  94818. hal/n-acetals
  94819. hal/o
  94820. hal/o
  94821. o/o-acetals
  94822. anomeric
  94823. centers
  94824. carbohydrates
  94825. hal/o-acetals
  94826. hal/s-acetals
  94827. halasa
  94828. halasa
  94829. schulz
  94830. mochel
  94831. organolithium
  94832. halazy
  94833. halbeek
  94834. halbritter
  94835. haldna
  94836. halenaquinone
  94837. halevi
  94838. halevi
  94839. amitai
  94840. orbital
  94841. symmetry
  94842. reaction
  94843. mechanism
  94844. haley
  94845. century
  94846. radical
  94847. chemistry
  94848. halgas
  94849. halgas
  94850. biocatalysts
  94851. organic
  94852. synthesis
  94853. studies
  94854. haliclonadiamine
  94855. halicondrin
  94856. halid
  94857. halide
  94858. halide
  94859. based
  94860. electrophiles
  94861. mediated
  94862. epoxide
  94863. opening
  94864. halidesC
  94865. phosphorus
  94866. stereochemistry
  94867. mechanistic
  94868. hallberg
  94869. haller
  94870. haller-bauer
  94871. halloallenes
  94872. hallucinogens
  94873. halo-substituted
  94874. haloacetals
  94875. haloacetylenes
  94876. haloaldimines
  94877. haloalkyl
  94878. haloalkyl
  94879. isothiocyanates
  94880. useful
  94881. versatile
  94882. reage
  94883. haloallyllithium
  94884. haloamides
  94885. haloaryl
  94886. haloboranes
  94887. haloboranes
  94888. their
  94889. alkyl
  94890. derivatives
  94891. haloboration
  94892. haloboration
  94893. application
  94894. organic
  94895. synthesis
  94896. halocarbenes
  94897. halocarbenoids
  94898. halocarbons
  94899. halochromism
  94900. halocyclization
  94901. halocyclopropanes
  94902. halocyclopropanes
  94903. halocarbenes
  94904. halocyclopropanes
  94905. halocarbenes
  94906. william
  94907. parham
  94908. halodiaziridines
  94909. halodiazirines
  94910. haloenamines
  94911. haloenamines
  94912. haloesters
  94913. haloethanes
  94914. haloformates
  94915. halogen
  94916. halogen
  94917. fluoride
  94918. organic
  94919. synthesis
  94920. halogen-bond
  94921. halogen-containing
  94922. halogen-containing
  94923. carbenes
  94924. halogen-lithium
  94925. halogen-metal
  94926. halogenated
  94927. halogenated
  94928. ketenes
  94929. valuable
  94930. intermediates
  94931. organic
  94932. synthe
  94933. halogenation
  94934. halogenation
  94935. heterocycles
  94936. seven-membered
  94937. rings
  94938. halogenation
  94939. heterocycles
  94940. heterocycles
  94941. fused
  94942. other
  94943. halogenation
  94944. heterocyclies
  94945. five-membered
  94946. rings
  94947. halogenation
  94948. using
  94949. quaternary
  94950. ammonium
  94951. polyhalides
  94952. iodin
  94953. halogenation
  94954. using
  94955. quaternary
  94956. ammonium
  94957. polyhalides
  94958. halogeno
  94959. halogenoacetates
  94960. halogenoacetylenes
  94961. halogenoalkyl
  94962. halogenoalkyl
  94963. complexes
  94964. transition
  94965. metals
  94966. halogenoallenes
  94967. halogenocarbons
  94968. halogenomethylenepho
  94969. halogenonitroalkanes
  94970. halogenopyruvamides
  94971. halogenoquinolines
  94972. halogenosilanes
  94973. halogens
  94974. halohydrins
  94975. haloindolenines
  94976. haloiodobenzenes
  94977. haloketenes
  94978. haloketone
  94979. haloketones
  94980. halolactones
  94981. halomalondialdehydes
  94982. halomethanes
  94983. halomethyl
  94984. halonitroso
  94985. halopyridines
  94986. halosilanes
  94987. halosulfonium
  94988. halosulphonium
  94989. halotetrafluoroethyl
  94990. halovinylene
  94991. halovinylene
  94992. carbonates
  94993. organic
  94994. synthesis
  94995. halpern
  94996. halpern
  94997. application
  94998. aldehyde
  94999. ketone
  95000. condensates
  95001. halsted
  95002. halstenberg
  95003. halton
  95004. halton
  95005. brian
  95006. preface
  95007. strain
  95008. organic
  95009. chemistry
  95010. perspecti
  95011. hamada
  95012. hamada
  95013. hamana
  95014. hamatla
  95015. hamid
  95016. hamill
  95017. hamilton
  95018. hamilton
  95019. synthetic
  95020. studies
  95021. molecular
  95022. recognition
  95023. hamish
  95024. hamlin
  95025. hammerich
  95026. hammett
  95027. hammett/winstein
  95028. hammick
  95029. hammick
  95030. cyclizations
  95031. studies
  95032. mechanism
  95033. hammick
  95034. hammond
  95035. hamon
  95036. hampden
  95037. hamprecht
  95038. hamprecht
  95039. konig
  95040. stubenrauch
  95041. alkylsulfamoyl
  95042. chlorides
  95043. hamza
  95044. hanack
  95045. hanack
  95046. mechanistic
  95047. preparative
  95048. aspects
  95049. vinyl
  95050. cation
  95051. hanaoka
  95052. hanaya
  95053. handbook
  95054. handbook
  95055. enantioselective
  95056. catalysis
  95057. products
  95058. handbook
  95059. organophosphorus
  95060. chemistry
  95061. handedness
  95062. handhook
  95063. handling
  95064. handlon
  95065. handwerker
  95066. haneishi
  95067. hanessian
  95068. hanessian
  95069. approaches
  95070. total
  95071. synthesis
  95072. natural
  95073. hanford
  95074. hanin
  95075. hanke
  95076. hanna
  95077. hannes
  95078. hansch
  95079. hansch
  95080. substituent
  95081. constants
  95082. correlation
  95083. analysi
  95084. hansch
  95085. corwin
  95086. quantitative
  95087. structure
  95088. activity
  95089. relationships
  95090. hansen
  95091. hansen
  95092. organic
  95093. chemistry
  95094. atmosphere
  95095. hansen
  95096. carbon
  95097. hydrogen
  95098. coupling
  95099. constants
  95100. hansonZ
  95101. hanson
  95102. oliveira
  95103. stevioside
  95104. related
  95105. sweet
  95106. hanson
  95107. diterpenoids
  95108. natural
  95109. product
  95110. report
  95111. hanson
  95112. diterpenoids
  95113. sesterterpenoids
  95114. second
  95115. supplemeZ
  95116. hanson
  95117. diterpenoids
  95118. natural
  95119. hanson
  95120. diterpenoids
  95121. natural
  95122. product
  95123. reports
  95124. 199310
  95125. hanson
  95126. steroid
  95127. reactions
  95128. partial
  95129. synthesis
  95130. 199310
  95131. hanson
  95132. steroids
  95133. reactions
  95134. partial
  95135. syntheses
  95136. hanson
  95137. microbiological
  95138. transformation
  95139. diterpenoid
  95140. hanson
  95141. heteroaromatic
  95142. radicals
  95143. radicals
  95144. group
  95145. hanson
  95146. heteroaromatic
  95147. radicals
  95148. general
  95149. properties
  95150. hanson
  95151. robert
  95152. synthetic
  95153. methodology
  95154. nonracernic
  95155. hanspeter
  95156. hantzsch
  95157. hanusa
  95158. hanusa
  95159. timothy
  95160. ligand
  95161. influences
  95162. structure
  95163. reactivi
  95164. haoyun
  95165. hapalindole
  95166. hapman
  95167. happel
  95168. harada
  95169. harada
  95170. enantiodifferentiati
  95171. transformation
  95172. prochi
  95173. harada
  95174. toshiro
  95175. akira
  95176. enantiodifferentiati
  95177. transformation
  95178. harald
  95179. harayama
  95180. harborne
  95181. harborne
  95182. advances
  95183. chemical
  95184. ecology
  95185. natural
  95186. product
  95187. harborne
  95188. jeffrey
  95189. barry
  95190. flavonoids
  95191. advances
  95192. researc
  95193. harcourt
  95194. harcourt
  95195. richard
  95196. valence
  95197. structures
  95198. organic
  95199. chemi
  95200. harding
  95201. hardy
  95202. hardy
  95203. protecting
  95204. groups
  95205. peptide
  95206. synthesis
  95207. hargittai
  95208. hargrave
  95209. harikisan
  95210. haritos
  95211. harmon
  95212. harmon
  95213. asymmetry
  95214. carbohydrates
  95215. marcel
  95216. dekker
  95217. harmony
  95218. harmony
  95219. marlin
  95220. elusive
  95221. equilibrium
  95222. length
  95223. harns
  95224. harold
  95225. harper
  95226. harpp
  95227. harre
  95228. harring
  95229. harring
  95230. scott
  95231. edstrom
  95232. livinghouse
  95233. episulfonium
  95234. harrington
  95235. harris
  95236. harris
  95237. kenneth
  95238. molecular
  95239. confinement
  95240. harrison
  95241. harrod
  95242. harry
  95243. simple
  95244. enols
  95245. chemical
  95246. reviews
  95247. review
  95248. harold
  95249. iptycenes
  95250. cuppedophanes
  95251. cappedophanes
  95252. hartley
  95253. hartley
  95254. frank
  95255. chemistry
  95256. organophosphorus
  95257. compoun
  95258. hartmann
  95259. hartmut
  95260. hartog
  95261. hartung
  95262. hartwig
  95263. hartzler
  95264. harumasa
  95265. haruo
  95266. harvey
  95267. harvey
  95268. activated
  95269. metabolites
  95270. carcinogenic
  95271. hydrocarbon
  95272. harvey
  95273. ronald
  95274. polycyclic
  95275. aromatic
  95276. hydrocarbons
  95277. cambridge
  95278. harwood
  95279. harwood
  95280. laurence
  95281. polar
  95282. rearrangements
  95283. oxford
  95284. university
  95285. hasan
  95286. koskimies
  95287. compilation
  95288. references
  95289. formyl
  95290. hasegawa
  95291. haselbach
  95292. hashemi
  95293. hashimoto
  95294. haslam
  95295. haslam
  95296. activation
  95297. protection
  95298. carbonyl
  95299. group
  95300. haslam
  95301. plant
  95302. polyphenols
  95303. vegetable
  95304. tannins
  95305. gallic
  95306. haslam
  95307. plant
  95308. polyphenols
  95309. vegetable
  95310. tannins
  95311. gallic
  95312. haslam
  95313. recent
  95314. developments
  95315. methods
  95316. esterificati
  95317. haslam
  95318. edwin
  95319. shikimic
  95320. metabolism
  95321. metabolites
  95322. wiley
  95323. hassall
  95324. hassan
  95325. hassanaly
  95326. hassel
  95327. hassenruck
  95328. hassner
  95329. hassner
  95330. alexanian
  95331. recent
  95332. aspects
  95333. azirine
  95334. chemistry
  95335. hassner
  95336. stumer
  95337. organic
  95338. syntheses
  95339. based
  95340. reactions
  95341. hassner
  95342. alfred
  95343. fischer
  95344. bilha
  95345. chemistryof
  95346. oxazoles
  95347. hetero
  95348. hasubanan
  95349. hasumi
  95350. hatanaka
  95351. hatanaka
  95352. amino
  95353. acids
  95354. mushrooms
  95355. 1992591
  95356. hatanaka
  95357. yasuo
  95358. hiyama
  95359. tamejiro
  95360. highly
  95361. selective
  95362. cross
  95363. coupli
  95364. hatano
  95365. hathway
  95366. hathway
  95367. importance
  95368. enzymic
  95369. chemical
  95370. reaction
  95371. hatlevig
  95372. haubenstock
  95373. haufe
  95374. haufe
  95375. chemistry
  95376. alicyclic
  95377. compounds
  95378. structure
  95379. hauser
  95380. hausler
  95381. haver
  95382. having
  95383. havinga
  95384. havinga
  95385. egbert
  95386. enjoying
  95387. organic
  95388. chemistry
  95389. profiles
  95390. havlas
  95391. hawkins
  95392. haworth
  95393. haworth
  95394. memorial
  95395. lecture
  95396. exper
  95397. ments
  95398. directed
  95399. towards
  95400. glycoc
  95401. hayakawa
  95402. hayashi
  95403. hayashi
  95404. higashino
  95405. reactions
  95406. aromatic
  95407. heterocycles
  95408. hayashi
  95409. tamio
  95410. akihiko
  95411. ozawa
  95412. fumiyuki
  95413. catalytic
  95414. asymmetr
  95415. hayashi
  95416. tamio
  95417. akihito
  95418. ozawa
  95419. fumiyuki
  95420. catalytic
  95421. asymmetr
  95422. hayashi
  95423. tamio
  95424. uozumi
  95425. yasuhiro
  95426. catalytic
  95427. asymmetric
  95428. synthesis
  95429. hayashida
  95430. hayatsu
  95431. hayden
  95432. hayes
  95433. haynes
  95434. hayward
  95435. hazai
  95436. hazai
  95437. laszlo
  95438. isoquinolones
  95439. their
  95440. saturated
  95441. derivati
  95442. hdides
  95443. health
  95444. healthy
  95445. heaney
  95446. heaney
  95447. harry
  95448. novel
  95449. organic
  95450. peroxygen
  95451. reagents
  95452. hearing
  95453. hearn
  95454. heart
  95455. heath
  95456. heathcock
  95457. heathcock
  95458. clayton
  95459. enchanting
  95460. alkaloids
  95461. yuzuriha
  95462. heating
  95463. heats
  95464. heavy
  95465. heavy-metal
  95466. heavy-metal
  95467. organic
  95468. chemistry
  95469. building
  95470. hebecker
  95471. hecht
  95472. hechtberger
  95473. palladium
  95474. catalyzed
  95475. reactions
  95476. organic
  95477. halides
  95478. reactions
  95479. water
  95480. hecker
  95481. hoffmann
  95482. tobacco
  95483. specific
  95484. nitrosamines
  95485. hector
  95486. heelis
  95487. heftmann
  95488. heftmann
  95489. erich
  95490. chromatography
  95491. damentals
  95492. heftmann
  95493. erich
  95494. chromatography
  95495. fundamentals
  95496. hegarty
  95497. hegarty
  95498. stereospecific
  95499. reactions
  95500. nitrilium
  95501. hegedus
  95502. hehre
  95503. hehre's
  95504. heicklen
  95505. heidelberg
  95506. heiden
  95507. heidlberg
  95508. heightened
  95509. heightened
  95510. selectivity
  95511. aromatic
  95512. nitrations
  95513. chlorinati
  95514. heigl
  95515. heilbronner
  95516. heilbronner
  95517. edgar
  95518. dunitz
  95519. reflections
  95520. symmetry
  95521. heimbach
  95522. heimbach
  95523. schenkluhn
  95524. controlling
  95525. factors
  95526. homogenous
  95527. heimer
  95528. heimgartner
  95529. heimgartner
  95530. heinz
  95531. amino
  95532. azirine
  95533. synthons
  95534. alpha
  95535. heine
  95536. heinekey
  95537. heinekey
  95538. oldham
  95539. warren
  95540. coordination
  95541. chemistry
  95542. heinisch
  95543. heinrich
  95544. heinz
  95545. heldt
  95546. helena
  95547. helerocycles
  95548. helgard
  95549. heliannuol
  95550. heliantheae
  95551. helical
  95552. hegarty
  95553. stereospecific
  95554. reactions
  95555. nitrilium
  95556. helically@
  95557. helicating@
  95558. hemiesters@
  95559. henk@
  95560. hepta-25-dienes@
  95561. herbert
  95562. herrmann
  95563. hydroxycinnamic
  95564. hydroxybenzoic
  95565. hetero
  95566. hetero
  95567. diels-alder
  95568. methodology
  95569. organic
  95570. synthesis@
  95571. heteroaromatic
  95572. heteroaromatic
  95573. ortho-quinodimethane@
  95574. heteroatom
  95575. heteroatom-stabilize@
  95576. heteroatoms@
  95577. heterocycles
  95578. heterocycles
  95579. molecular
  95580. recognition@
  95581. heterocyclic
  95582. metal
  95583. heterodienes@
  95584. heterolytic
  95585. fragmentation
  95586. organic
  95587. molecules@
  95588. hetroaromatic@
  95589. hewitt@
  95590. hiberty
  95591. ohanessian
  95592. shaik
  95593. flament
  95594. delocaliz@
  95595. intensity
  95596. laser
  95597. photochemistry
  95598. organic
  95599. molecules
  95600. pressure
  95601. kinetic
  95602. investigations
  95603. organic
  95604. macromol@
  95605. higher
  95606. fluorides
  95607. group
  95608. elements
  95609. fluorinating
  95610. highly
  95611. helicating
  95612. helicene
  95613. helicenes
  95614. helices
  95615. helices
  95616. supramolecular
  95617. chemistry
  95618. metal-directed
  95619. helix
  95620. heller
  95621. heller
  95622. photochromic
  95623. compounds
  95624. optical
  95625. information
  95626. heller
  95627. homoisoflavanones
  95628. biogenetically
  95629. relate
  95630. hellier
  95631. hellman
  95632. hellmann
  95633. hellmut
  95634. helmanek
  95635. helmchen
  95636. helmer
  95637. helmut
  95638. helpful
  95639. helquist
  95640. helquist
  95641. bergdahl
  95642. gangloff
  95643. demillequand
  95644. helsen
  95645. helson
  95646. helvetica
  95647. hemagglutinin
  95648. hemethiolate
  95649. hemiacetal
  95650. hemiacetals
  95651. hemistry
  95652. hemiswinholide
  95653. hemiterpenes
  95654. hemmer
  95655. hemmerich
  95656. hemmi
  95657. hemoproteins
  95658. henderson
  95659. hendrickson
  95660. hendrickson
  95661. james
  95662. descriptions
  95663. reactions
  95664. their
  95665. logic
  95666. hendrix
  95667. heneicosen
  95668. henne
  95669. hennen
  95670. henning
  95671. henri
  95672. henrici
  95673. henrick
  95674. henry
  95675. henry
  95676. palladium
  95677. catalyzed
  95678. oxidation
  95679. hydrocarbons
  95680. henschler
  95681. henschler
  95682. toxicity
  95683. chlorinated
  95684. organic
  95685. compounds
  95686. effect
  95687. hense
  95688. henze
  95689. heparin
  95690. hepaticae
  95691. hept-5-en-2-yl
  95692. hepta
  95693. hepta-2.5-dienes
  95694. hepta-46-dienes
  95695. heptadienes
  95696. heptadienyl
  95697. heptafulvalenes
  95698. heptafulvenes
  95699. heptalene
  95700. heptane
  95701. heptanes
  95702. heptanones
  95703. heptanyl
  95704. heptasaccharide
  95705. heptatriafulvenes
  95706. heptene
  95707. heptenes
  95708. heptyl
  95709. herbarium
  95710. herbert
  95711. herbert
  95712. herbert
  95713. biosynthesis
  95714. secondary
  95715. metabolites
  95716. chapman
  95717. herbert
  95718. biosynthesis
  95719. plant
  95720. alkaloids
  95721. nitrogen
  95722. herbertane
  95723. herbs
  95724. herbst
  95725. herbst
  95726. willy
  95727. hunger
  95728. klaus
  95729. industrial
  95730. organic
  95731. pigments
  95732. produc
  95733. herczegh
  95734. hererocyclic
  95735. herfried
  95736. herges
  95737. herges
  95738. rainer
  95739. organizing
  95740. principle
  95741. complex
  95742. reactions
  95743. hergott
  95744. hericenes
  95745. heritol
  95746. heritonin
  95747. herman
  95748. hermann
  95749. hermecz
  95750. hermecz
  95751. istvan
  95752. kereszturi
  95753. vasvari
  95754. debreczy
  95755. lelle
  95756. aminom
  95757. hermenegildo
  95758. hernandez
  95759. herndon
  95760. herndon
  95761. james
  95762. tumer
  95763. seniz
  95764. mcmullen
  95765. leonard
  95766. matasi
  95767. herndon
  95768. james
  95769. kreutzer
  95770. kristina
  95771. herout
  95772. herrmann
  95773. herrmann
  95774. hydroxycinnamic
  95775. hydroxybenzoic
  95776. herrmann
  95777. hydroxycinnamic
  95778. hydroxybenzoic
  95779. herrmann
  95780. organometallic
  95781. syntheses
  95782. diazoalkanes
  95783. herrmann
  95784. wolfgang
  95785. kohlpaintner
  95786. christian
  95787. water
  95788. soluble
  95789. herscheid
  95790. herunsalee
  95791. herve
  95792. biogenetic
  95793. aspects
  95794. sesquiterpene
  95795. lactone
  95796. chemistry
  95797. hesis
  95798. heskamp
  95799. translated
  95800. german
  95801. alkaloid
  95802. chemistry
  95803. hesse
  95804. hesse
  95805. manfred
  95806. enlargement
  95807. organic
  95808. chemistry
  95809. hesse
  95810. application
  95811. fluoroxy
  95812. compounds
  95813. organic
  95814. synth
  95815. hetarenes
  95816. hetarenium
  95817. hetaryl
  95818. hetarylformazans
  95819. hetarynes
  95820. heter
  95821. heteriannulation
  95822. heterow
  95823. hetero
  95824. ls-alder
  95825. methodology
  95826. organic
  95827. synthesis
  95828. hetero-13-dienes
  95829. hetero-aromaticity
  95830. hetero-atoms
  95831. hetero-bimetallic
  95832. hetero-cope
  95833. hetero-diels-alder
  95834. hetero-diels-alder
  95835. reaction
  95836. highly
  95837. functionalized
  95838. natural
  95839. hetero-diels-alder
  95840. reactions
  95841. nitroso
  95842. dienophiles
  95843. applic
  95844. hetero-substituted
  95845. heteroadamantane
  95846. heteroadamantanes
  95847. heteroalkylation
  95848. heteroallenes
  95849. heteroallylic
  95850. heteroanalogous
  95851. heteroanalogues
  95852. heteroannelation
  95853. heteroannulation
  95854. heteroannulation
  95855. unsaturated
  95856. carbene
  95857. complexes
  95858. heteroannulations
  95859. heteroannulations
  95860. ortho-aminoaldehydes
  95861. heteroannulenes
  95862. heteroarenes
  95863. heteroarenes
  95864. general
  95865. introduction
  95866. heteroarenes
  95867. general
  95868. introduction
  95869. heteroarenes
  95870. general
  95871. introduction
  95872. heteroaromatic
  95873. heteroaromatic
  95874. oaromatic
  95875. ortho-quinodimethane
  95876. heteroaromatic
  95877. photosubstitutions
  95878. heteroaromatic
  95879. sulfoxides
  95880. sulfones
  95881. ligand
  95882. exchange
  95883. heteroaromatic-fused
  95884. heteroaromatic-fused
  95885. 3-sulfolenes
  95886. heteroaromatics
  95887. heteroaryl
  95888. heteroarylalkylation
  95889. heteroarylaminosulfa
  95890. heteroarylnitrenes
  95891. heteroaryltrimethyls
  95892. heteroat
  95893. heteroatom
  95894. heteroatom
  95895. heteroatom
  95896. assisted
  95897. isomerization
  95898. epoxides
  95899. allylic
  95900. heteroatom
  95901. directed
  95902. metallations
  95903. heterocyclic
  95904. synthesis
  95905. heteroatom
  95906. facilitated
  95907. lithiations
  95908. heteroatom
  95909. nucleophiles
  95910. metal-activated
  95911. alkenes
  95912. heteroatom-directed
  95913. heteroatom-directed
  95914. metallations
  95915. heterocyclic
  95916. synthesis
  95917. heteroatom-facilitat
  95918. heteroatom-facilitat
  95919. lithiations
  95920. heteroatom-stabilize
  95921. heteroatom-stabilize
  95922. allylic
  95923. anions
  95924. heteroatom-substitut
  95925. heteroatomic
  95926. oatoms
  95927. heteroatomsubstituen
  95928. heteroatomsubstitute
  95929. heterobenzenes
  95930. heterobi
  95931. heterobifunctional
  95932. heterobimetallic
  95933. heterocarbanions
  95934. heterocarboranes
  95935. heterochain
  95936. heterocope
  95937. heterocope
  95938. rearrangements
  95939. phenyl
  95940. vinylhydroxylamine
  95941. heterocumulene
  95942. heterocumulenes
  95943. heterocycl
  95944. heterocycle
  95945. heterocycle
  95946. synthesis
  95947. palladium
  95948. catalysed
  95949. cyclisation
  95950. heterocycles
  95951. heterocycles
  95952. heterocycles
  95953. heterocycles
  95954. heterocycles
  95955. containing
  95956. sulfamide
  95957. moiety
  95958. heterocycles
  95959. fused
  95960. 23-bond
  95961. benzopyran
  95962. heterocycles
  95963. replication
  95964. assembly
  95965. heterocycles1991
  95966. heterocycli
  95967. heterocyclic
  95968. heterocyclic
  95969. heterocyclic
  95970. heterocyclic
  95971. analogues
  95972. methylanecyclopropan
  95973. heterocyclic
  95974. aromaticity
  95975. heterocyclic
  95976. betain
  95977. derivatives
  95978. alternate
  95979. hydrocarbons
  95980. heterocyclic
  95981. chemistry
  95982. heterocyclic
  95983. dithiocarboxylic
  95984. acids
  95985. heterocyclic
  95986. enamino
  95987. esters
  95988. versatile
  95989. synthons
  95990. heterocycl
  95991. heterocyclic
  95992. fragmentation
  95993. organic
  95994. molecules
  95995. heterocyclic
  95996. intermediates
  95997. products
  95998. formed
  95999. oxidative
  96000. heterocyclic
  96001. ketene
  96002. aminals
  96003. heterocyclic
  96004. n-oxides
  96005. heterocyclic
  96006. n-oxides
  96007. n-imides
  96008. heterocyclic
  96009. quinones
  96010. heterocyclic
  96011. rearrangements
  96012. benzofuroxans
  96013. related
  96014. heterocyclic
  96015. rings
  96016. containing
  96017. transition
  96018. metal
  96019. heterocyclic
  96020. rings
  96021. containing
  96022. transition
  96023. metal
  96024. heterocyclic
  96025. rings
  96026. containing
  96027. arsenic
  96028. antimony
  96029. bismuth
  96030. heterocyclic
  96031. rings
  96032. containing
  96033. boron
  96034. heterocyclic
  96035. rings
  96036. containing
  96037. halogens
  96038. heterocyclic
  96039. rings
  96040. containing
  96041. phosphorus
  96042. heterocyclic
  96043. rings
  96044. containing
  96045. silicon
  96046. germanium
  96047. heterocyclic
  96048. sonochemistry
  96049. heterocyclic
  96050. syntheses
  96051. based
  96052. aromatic
  96053. lithiation
  96054. heterocyclic
  96055. synthesis
  96056. using
  96057. heterodienophiles
  96058. heterocyclic
  96059. synthesis
  96060. azides
  96061. reactions
  96062. triazoline
  96063. heterocyclic
  96064. systems
  96065. containing
  96066. bridgehead
  96067. nitrogen
  96068. heterocyclic
  96069. systems
  96070. containing
  96071. bridgehead
  96072. nitrogen
  96073. heterocyclies
  96074. heterocyclization
  96075. heterocyclizations
  96076. heterocyclo
  96077. heterocycloaddition
  96078. heterocycloalkyliden
  96079. heterocyclophanes
  96080. heterocyclopolyaroma
  96081. heterocyclyl
  96082. heterodiene
  96083. heterodiene
  96084. additions
  96085. heterodienes
  96086. heterodienophile
  96087. heterodienophile
  96088. additions
  96089. dienes
  96090. heterodienophiles
  96091. heterodinuclear
  96092. heteroelement
  96093. heteroepins
  96094. heterofunctional
  96095. heterofunctionally
  96096. heterogeneous
  96097. heterogeneous
  96098. catalytic
  96099. hydrogenation
  96100. alkynes
  96101. heterogeneous
  96102. organic
  96103. synthesis
  96104. using
  96105. functionalised
  96106. polymer
  96107. heterogeneous
  96108. platinum-catalyzed
  96109. hydrogenations
  96110. diolefin
  96111. heterogeneous-cataly
  96112. heterogenous
  96113. heterogenous
  96114. catalytic
  96115. transfer
  96116. hydrogenation
  96117. reduction
  96118. heteroleptic
  96119. heteroleptic
  96120. diorganozinc
  96121. compounds
  96122. me3si
  96123. heteroles
  96124. heterolysis
  96125. heterolytic
  96126. heterolytic
  96127. fragmentation
  96128. class
  96129. organic
  96130. reactions
  96131. heterolytic
  96132. fragmentation
  96133. organic
  96134. molecules
  96135. heteromet
  96136. heterometallic
  96137. heteromonocycles
  96138. heteronuclear
  96139. heteronuclear
  96140. cluster
  96141. chemistry
  96142. copper
  96143. silver
  96144. heteroorganosulfoniu
  96145. heteropentalenes
  96146. heterophanes
  96147. heterophospholes
  96148. heteropoly
  96149. heteropolyacid
  96150. heteropolycompounds
  96151. heteropolynuclear
  96152. heteroprostanoids
  96153. heteroquadricyclanes
  96154. heteroradialenes
  96155. heterosiloxanes
  96156. heterosubstituted
  96157. heterosubstituted
  96158. allenes
  96159. polyallenes
  96160. heterosubstituted
  96161. nitroalkenes
  96162. synthesis
  96163. heterotricyclic
  96164. heterotriorgano
  96165. heterotriorgano
  96166. tetraorganosulfurane
  96167. heterovinylogues
  96168. heteroyohimboid
  96169. heteryne
  96170. hetic
  96171. hetrocycles
  96172. heuristic
  96173. hevesi
  96174. heweson[
  96175. heweson
  96176. sesquiterpenoids
  96177. second
  96178. supplements
  96179. hewitt
  96180. hewlins
  96181. hexaalkoxides
  96182. hexacarbonyl-diiron
  96183. hexacoordinate
  96184. hexacoordinated
  96185. hexadecyl
  96186. hexadiyne
  96187. hexafluoropropene
  96188. hexahydropyridazine
  96189. hexahydrotriazines
  96190. hexahydroxydiphenic
  96191. hexamethyl12
  96192. hexamethyldisilathia
  96193. hexamethyldisilazane
  96194. hexamethyldisilazide
  96195. hexamethylenetetrami
  96196. hexamethylenetetrami
  96197. versatile
  96198. reagent
  96199. organic
  96200. synthesi
  96201. hexamethylphosphoram
  96202. hexan
  96203. hexane
  96204. hexanediol
  96205. hexanes
  96206. hexaorganotelluriums
  96207. hexatrienes
  96208. hexatriyne
  96209. hexavalent
  96210. hexenec
  96211. hexenuloses
  96212. hexenylalkalis
  96213. hexenylamines
  96214. hexenyllithium
  96215. hexenyllithiums
  96216. hexitols
  96217. hexonolactones
  96218. hexopyranosides
  96219. hexoses
  96220. hexyl
  96221. heyde
  96222. heyden
  96223. hibbert
  96224. hiberty
  96225. hiberty
  96226. ohanessian
  96227. shaik
  96228. flament
  96229. delocaliz
  96230. hibino
  96231. hickmott
  96232. hicks
  96233. hickson
  96234. hidden
  96235. hideg
  96236. hideji
  96237. hideki
  96238. hidemasa
  96239. hidemitsu
  96240. hidenori
  96241. hideo
  96242. hiemstra
  96243. phenolic
  96244. substances
  96245. marine
  96246. natural
  96247. products
  96248. higashino
  96249. intensity
  96250. laser
  96251. photochemistry
  96252. organic
  96253. molecules
  96254. pressure
  96255. diels
  96256. alder
  96257. reaction
  96258. fullerene
  96259. pressure
  96260. intermolecular
  96261. diels
  96262. alder
  96263. reactions
  96264. pressure
  96265. kinetic
  96266. investigations
  96267. organic
  96268. macromol
  96269. temperature
  96270. radical
  96271. cyclization
  96272. anomalies
  96273. tandem
  96274. yields
  96275. nitrene
  96276. insertion
  96277. unactivated
  96278. bonds
  96279. high-oxidation-state
  96280. high-oxidation-state
  96281. molybdenum
  96282. tungsten
  96283. alkylidene
  96284. high-pressure
  96285. higher
  96286. fluorides
  96287. group
  96288. elements
  96289. fluorinating
  96290. higher
  96291. order
  96292. cyanocuprate
  96293. structure
  96294. cyanide
  96295. lithium
  96296. bound
  96297. higher-order
  96298. highlights
  96299. highly
  96300. highly
  96301. highly
  96302. stereoselectivity
  96303. asymmetric
  96304. radical
  96305. addition
  96306. highly
  96307. chemoselective
  96308. allylation
  96309. carbonyl
  96310. compounds
  96311. highly
  96312. chemoselective
  96313. reduction
  96314. protected
  96315. lactams
  96316. highly
  96317. diastereoselective
  96318. acetal
  96319. cleavages
  96320. using
  96321. novel
  96322. reage
  96323. highly
  96324. diastereoselective
  96325. addition
  96326. organometallic
  96327. reagent
  96328. highly
  96329. diastereoselective
  96330. hydrocyanation
  96331. sulfinylcycloa
  96332. highly
  96333. diastereoselective
  96334. sequential
  96335. enolate-michael
  96336. additio
  96337. highly
  96338. diastereoselective
  96339. synthesis
  96340. oxazoline
  96341. carboxy
  96342. highly
  96343. efficient
  96344. synthesis
  96345. nitrones
  96346. catalytic
  96347. highly
  96348. efficient
  96349. intramolecular
  96350. general
  96351. catalysis
  96352. highly
  96353. efficient
  96354. method
  96355. epoxidation
  96356. olefins
  96357. highly
  96358. efficient
  96359. synthesis
  96360. substituted
  96361. chromen
  96362. highly
  96363. efficient
  96364. synthesis
  96365. potent
  96366. antitumor
  96367. annonaceo
  96368. highly
  96369. enantioselective
  96370. alkynylation
  96371. aldehydes
  96372. promoted
  96373. highly
  96374. enantioselective
  96375. catalytic
  96376. asymmetric
  96377. automultiplicat
  96378. highly
  96379. enantioselective
  96380. catalytic
  96381. epoxidation
  96382. trisubstitu
  96383. highly
  96384. enantioselective
  96385. epoxidation
  96386. catalysts
  96387. derived
  96388. highly
  96389. enantioselective
  96390. hydroformylation
  96391. olefins
  96392. catalyze
  96393. highly
  96394. enantioselective
  96395. temperature
  96396. epoxidation
  96397. styre
  96398. highly
  96399. like-selective
  96400. cycloadditions
  96401. chiral
  96402. dienols
  96403. highly
  96404. reactive
  96405. arene
  96406. complexes
  96407. their
  96408. stoich
  96409. highly
  96410. reactive
  96411. intermediates
  96412. condensation
  96413. reaction
  96414. highly
  96415. reduced
  96416. metal
  96417. carbonyl
  96418. anions
  96419. synthesis
  96420. characterizat
  96421. highly
  96422. regio
  96423. diastereoselective
  96424. synthesis
  96425. highly
  96426. regio
  96427. stereoselective
  96428. alkylation
  96429. vic-bis
  96430. pheny
  96431. highly
  96432. regio
  96433. stereoselective
  96434. preparation
  96435. silyl
  96436. highly
  96437. regioselective
  96438. stereoselective
  96439. silylformylation
  96440. highly
  96441. regioselective
  96442. monoalkylation
  96443. ketones
  96444. manganes
  96445. highly
  96446. regioselective
  96447. palladium
  96448. mediated
  96449. substitution
  96450. highly
  96451. regioselective
  96452. reaction
  96453. zirconocene
  96454. alkene
  96455. complex
  96456. highly
  96457. selective
  96458. operationally
  96459. simple
  96460. synthesis
  96461. enant
  96462. highly
  96463. selective
  96464. cross
  96465. coupling
  96466. reactions
  96467. silan
  96468. highly
  96469. selective
  96470. cross
  96471. coupling
  96472. reactions
  96473. organosilicon
  96474. highly
  96475. selective
  96476. cross-coupling
  96477. reactions
  96478. organosilicon
  96479. highly
  96480. selective
  96481. enantiomer
  96482. differentiation
  96483. intramolecula
  96484. highly
  96485. selective
  96486. skeletal
  96487. reorganization
  96488. enynes
  96489. highly
  96490. selective
  96491. skeletal
  96492. reorganization
  96493. 17-enynes
  96494. highly
  96495. stereocontrolled
  96496. construction
  96497. alkoxyazetidin
  96498. highly
  96499. stereoselective
  96500. reaction
  96501. aldimines
  96502. highly
  96503. stereoselective
  96504. syntheses
  96505. arsenic
  96506. phosphorus
  96507. highly
  96508. stereoselective
  96509. synthesis
  96510. unsaturated
  96511. ketones
  96512. highly
  96513. stereoselective
  96514. total
  96515. synthesis
  96516. allopumiliotoxins
  96517. highperformance
  96518. highsmith
  96519. higly
  96520. higly
  96521. stereocontrolled
  96522. total
  96523. synthesis
  96524. allopumiliotoxin
  96525. higuchi
  96526. hiizu
  96527. hikino
  96528. hildebrandt
  96529. hilgenfeld
  96530. hillW
  96531. anthony
  96532. organotransition
  96533. metallic
  96534. chemistry
  96535. sulfur
  96536. lawrence
  96537. richards
  96538. christopher
  96539. saberi
  96540. stephen
  96541. thomas
  96542. dictionary
  96543. steroids
  96544. chemical
  96545. hillgaertner
  96546. hillier
  96547. hilmy
  96548. hilvert
  96549. hilvert
  96550. donald
  96551. antibody
  96552. catalysis
  96553. hilvert
  96554. donald
  96555. antibody
  96556. catalysis
  96557. carbon
  96558. carbon
  96559. himachalene
  96560. himbacine
  96561. himbelline
  96562. hindenlang
  96563. hindered
  96564. bifunctional
  96565. catalysis
  96566. alpha
  96567. hydrogen
  96568. exchange
  96569. hinrichs
  96570. hinton
  96571. hintze
  96572. hirama
  96573. hirao
  96574. hiraoka
  96575. hiraoka
  96576. michio
  96577. crown
  96578. ethers
  96579. analogous
  96580. compounds
  96581. studi
  96582. hiremath
  96583. hiremath
  96584. hooper
  96585. isatogens
  96586. indolones
  96587. hiroaki
  96588. hirobe
  96589. hirochika
  96590. hiroki
  96591. hiromichi
  96592. hirose
  96593. hiroshi
  96594. hirota
  96595. hiroyuki
  96596. hirsch
  96597. hirschmann
  96598. hirschmann
  96599. ralph
  96600. medicinal
  96601. chemistry
  96602. golden
  96603. hirsh
  96604. hirst
  96605. hirst
  96606. mechanisms
  96607. aromatic
  96608. nucleophilic
  96609. substitution
  96610. hisaeda
  96611. hisakazu
  96612. hisashi
  96613. hisatome
  96614. hisatome
  96615. masao
  96616. ferrocenophanes
  96617. multi
  96618. bridged
  96619. ferroc
  96620. histamine~
  96621. histidine
  96622. histochemistry
  96623. historical
  96624. history
  96625. histrionicotoxin
  96626. histrionicotoxins
  96627. hitachimycin
  96628. hitchcock
  96629. hitchings
  96630. hitesh
  96631. hitherto
  96632. hitomi
  96633. hitoshi
  96634. hitosi
  96635. hiv-i
  96636. hixson
  96637. hixson
  96638. photochemistry
  96639. cyclopropanes
  96640. organic
  96641. photochem
  96642. hiyama
  96643. hiyama
  96644. hatanaka
  96645. palladium
  96646. catalyzed
  96647. cross
  96648. coupling
  96649. react
  96650. hiyoshizo
  96651. hladka
  96652. hladka
  96653. jaroslav
  96654. kratochvll
  96655. milan
  96656. kvasnicka
  96657. vladimir
  96658. reductase
  96659. inhibitors
  96660. hmg-coa
  96661. hmg-coa
  96662. reductase
  96663. inhibitors
  96664. ogeneous
  96665. group-4
  96666. metallocene
  96667. ziegler-natta
  96668. catalysts
  96669. analysis
  96670. synthetic
  96671. reactions
  96672. principle
  96673. reduction
  96674. organic
  96675. compounds
  96676. valent
  96677. specie
  96678. enantioselective
  96679. synthesis
  96680. natural
  96681. products
  96682. heterolytic
  96683. fragmentation
  96684. organic
  96685. molecules
  96686. polarity
  96687. control
  96688. synthesis
  96689. wiley
  96690. tactics
  96691. organic
  96692. synthesis
  96693. wiley
  96694. tandem
  96695. organic
  96696. reactions
  96697. wiley
  96698. ho-te-oh
  96699. hoare
  96700. hobza
  96701. hodge
  96702. hodge
  96703. polymer
  96704. supported
  96705. protecting
  96706. groups
  96707. chemist
  96708. hodge
  96709. polymer
  96710. supports
  96711. organic
  96712. synthesis
  96713. hodge
  96714. sherington
  96715. polymer
  96716. supported
  96717. reactions
  96718. hodgson
  96719. hoeper
  96720. hoesch
  96721. hofelich
  96722. hofer
  96723. hoffmaiester
  96724. hoffman
  96725. hoffman
  96726. oxidative
  96727. attachment
  96728. arenesulfonyloxy
  96729. groups
  96730. hoffman
  96731. robert
  96732. synthetic
  96733. transformations
  96734. using
  96735. arenesulfon
  96736. hoffmann
  96737. hoffmann
  96738. stereochemistry
  96739. sigmatropic
  96740. rearrangemen
  96741. hofle
  96742. hofle
  96743. steglich
  96744. vorbruggen
  96745. dialkylaminopyridine
  96746. hofmann
  96747. eugen
  96748. enantioselective
  96749. epoxidation
  96750. peroxidic
  96751. oxyge
  96752. hogberg
  96753. hogen
  96754. hogeveen
  96755. hogeveen
  96756. kruchten
  96757. wagner
  96758. meerwein
  96759. rearrangemen
  96760. hohner
  96761. hoiness
  96762. holcomb
  96763. holden
  96764. holder
  96765. holdt
  96766. holdt
  96767. thiacrown
  96768. compounds
  96769. dicyano
  96770. dithioethen
  96771. hodge
  96772. sherington
  96773. polymer
  96774. supported
  96775. reactions
  96776. electron
  96777. transfer
  96778. catalyzed
  96779. pericyclic
  96780. reactions@
  96781. homoallyllithiums@
  96782. homochiral@
  96783. homogeneous
  96784. heterogeneous
  96785. catalytic
  96786. oxidations
  96787. pero@
  96788. homologation
  96789. homologous@
  96790. hoppe
  96791. hintze
  96792. tebben
  96793. paetow
  96794. ahrens
  96795. schwerdtfeger
  96796. hosomi
  96797. houshang@
  96798. chiral
  96799. sulfinylallyl
  96800. sulfinyl
  96801. ketimine
  96802. anion@
  96803. hudrlik
  96804. hudrlik
  96805. epoxysilanes
  96806. advances
  96807. hulshof
  96808. wynberg
  96809. vanishing
  96810. optical
  96811. activity
  96812. hurst
  96813. derek
  96814. nitration
  96815. phenyl
  96816. substituted
  96817. heterocycl@
  96818. hydrazines
  96819. hydride-titanium@
  96820. hydroarylation@
  96821. hydroboration
  96822. improved
  96823. procedure
  96824. synthesis
  96825. hydrocarbons
  96826. hydroformylation
  96827. related
  96828. additions
  96829. carbon
  96830. monoxide
  96831. hydrogen
  96832. hydrogenation
  96833. methods@
  96834. hydrogenations
  96835. hydroperoxides
  96836. hodge
  96837. sherington
  96838. polymer
  96839. supported
  96840. reactions
  96841. hydrosilylation@
  96842. fleming
  96843. frontier
  96844. orbitals
  96845. organic
  96846. chemical
  96847. reactions
  96848. search
  96849. carbene
  96850. icals
  96851. solution
  96852. reaction
  96853. pathw@
  96854. intersystem
  96855. crossing
  96856. triplet
  96857. biradicals
  96858. conformational@
  96859. introduction@
  96860. liebscher
  96861. hartmann
  96862. heterocycles
  96863. diary@
  96864. kaplan
  96865. trozzolo
  96866. singlet
  96867. oxygen
  96868. degrad@
  96869. ketimines@
  96870. kukushkin
  96871. deoxygenation
  96872. coordinated
  96873. sulfoxi@
  96874. lactones@
  96875. lewis
  96876. promoted
  96877. addition
  96878. reactions
  96879. organometallic
  96880. coordinate
  96881. carbene
  96882. complexes
  96883. nickel
  96884. platinum
  96885. macrocyclic
  96886. chemistry
  96887. aspects
  96888. organic
  96889. inorganic
  96890. supra@
  96891. mechanism
  96892. molybdenum
  96893. pentacarbonyl-cataly
  96894. cyclizations
  96895. mechanisms
  96896. stereochemistry
  96897. alkali
  96898. metal
  96899. reductions
  96900. morkovnik
  96901. okhlobystin
  96902. inorganic
  96903. radical
  96904. tations
  96905. benzene
  96906. electron
  96907. transfer
  96908. catalyzed
  96909. pericyclic
  96910. reactions
  96911. holger
  96912. holland
  96913. holland
  96914. microbial
  96915. vitro
  96916. enzymic
  96917. transformations
  96918. holland
  96919. herbert
  96920. organic
  96921. synthesis
  96922. oxidative
  96923. enzymes
  96924. hollas
  96925. hollas
  96926. michael
  96927. determination
  96928. molecular
  96929. conformation
  96930. holler
  96931. holler
  96932. protein
  96933. biosynthesis
  96934. codon
  96935. specific
  96936. activation
  96937. hollingsworth
  96938. hollow
  96939. holmes
  96940. holness
  96941. holton
  96942. holzmeier
  96943. homer
  96944. homo-aza-steroidal
  96945. homo-aza-steroids
  96946. homoaldol
  96947. homoallenylboration
  96948. homoallyl
  96949. homoallyl
  96950. cyanide
  96951. allylketene
  96952. imine
  96953. sigmatropic
  96954. homoallylamines
  96955. homoallylic
  96956. homoaza
  96957. homochiral
  96958. homochiral
  96959. compounds
  96960. sugars
  96961. homochiral
  96962. cycloadducts
  96963. derived
  96964. sugar
  96965. aldoximes
  96966. homocoupling
  96967. homocubane
  96968. homocubanes
  96969. homocubene
  96970. homocubylidene
  96971. homodienyl
  96972. homoenolate
  96973. homoenolate
  96974. anions
  96975. homoenolate
  96976. anion
  96977. equivalents
  96978. mechani
  96979. homoenolates
  96980. homoenolates
  96981. other
  96982. functionalized
  96983. organometallics
  96984. homoenolates
  96985. other
  96986. functionalized
  96987. organometallics
  96988. homog
  96989. homogeneity
  96990. homogeneous
  96991. homogeneous
  96992. heterogeneous
  96993. catalytic
  96994. oxidations
  96995. homogeneous
  96996. asymmetric
  96997. hydrogenation
  96998. homogeneous
  96999. catalysis
  97000. applications
  97001. chemistry
  97002. homogeneous
  97003. catalyt
  97004. hydrogenation
  97005. alkynes
  97006. homogeneous
  97007. catalytic
  97008. oxidation
  97009. o-substituted
  97010. anilines
  97011. homogeneous
  97012. catalytic
  97013. reactions
  97014. unsaturated
  97015. homogeneous
  97016. hydrogenation
  97017. homogeneous
  97018. hydrogenation
  97019. catalysts
  97020. organic
  97021. synthesis
  97022. homogeneous
  97023. metal-catalysis
  97024. organic
  97025. photochemistry
  97026. homogeneously
  97027. homogeneously
  97028. catalysed
  97029. hydrogenation
  97030. homogeneously
  97031. catalysed
  97032. insertion
  97033. reactions
  97034. homogenous
  97035. homogenous
  97036. phase
  97037. transfer
  97038. catalysed
  97039. carbonylation
  97040. reacti
  97041. homogenous
  97042. nickel
  97043. catalysed
  97044. olefin
  97045. hydrocyanation
  97046. homoisoflavanones
  97047. homolate
  97048. homolate
  97049. anions
  97050. homoenolate
  97051. anion
  97052. equivalents
  97053. mechanisti
  97054. homoleptic
  97055. homologated
  97056. homologating
  97057. homologation
  97058. homologation
  97059. homologation-allylbo
  97060. homolyses
  97061. homolysis
  97062. homolytic
  97063. homolytic
  97064. aromatic
  97065. hydroxylations
  97066. radiolysis
  97067. aqueous
  97068. homolytic
  97069. cyclizations
  97070. chloroalkenylamines
  97071. homolytically
  97072. homometallic
  97073. homonuclear
  97074. homopeptides
  97075. homophthalic
  97076. homopropargyl
  97077. homopropargylic
  97078. homosteroids
  97079. homotropylium
  97080. honda
  97081. honeyman
  97082. hongconin
  97083. honig
  97084. honkawa
  97085. hoopen
  97086. hooper
  97087. hopanoids
  97088. atoms
  97089. reactive
  97090. molecules
  97091. closed
  97092. system
  97093. angew
  97094. henning
  97095. gerhard
  97096. preparation
  97097. properties
  97098. reactio
  97099. henning
  97100. witulski
  97101. bernhard
  97102. cyanoalkynes
  97103. magic
  97104. wands
  97105. hopkinson
  97106. hoppe
  97107. hoppe
  97108. hintze
  97109. tebben
  97110. paetow
  97111. ahrens
  97112. schwerdtfeger
  97113. horacio
  97114. horak
  97115. horeau
  97116. horeau
  97117. determination
  97118. configuration
  97119. secondary
  97120. horenstein
  97121. horizons
  97122. hormonal
  97123. hormone
  97124. hormones
  97125. hornbuckle
  97126. hornby
  97127. hornby
  97128. michael
  97129. peach
  97130. josephine
  97131. foundations
  97132. organic
  97133. chemis
  97134. horner
  97135. hornfeldt
  97136. horst
  97137. horton
  97138. horvath
  97139. horvath
  97140. molecular
  97141. design
  97142. chemical
  97143. structure
  97144. generation
  97145. horvath
  97146. istvan
  97147. millar
  97148. under
  97149. pressure
  97150. horwell
  97151. horwell
  97152. synthetic
  97153. strategies
  97154. ergoline
  97155. system
  97156. horwitz
  97157. horwood
  97158. hoshino
  97159. hosmane
  97160. hosokawa
  97161. hosokawa
  97162. takahiro
  97163. murahashi
  97164. shunichi
  97165. synthesis
  97166. oxygen
  97167. hosomi
  97168. hosomi
  97169. hosoya
  97170. vogtle
  97171. template
  97172. syntheses
  97173. angewandte
  97174. chemie
  97175. interna
  97176. guest
  97177. complexes
  97178. azaaromatic
  97179. quaternary
  97180. salts
  97181. host-guest
  97182. host-guest
  97183. complexes
  97184. azaaromatic
  97185. quaternary
  97186. salts
  97187. hostettmann
  97188. hosts
  97189. hough
  97190. houghton
  97191. houghton
  97192. metal
  97193. complexes
  97194. organic
  97195. chemistry
  97196. cambridge
  97197. theoretical
  97198. experimental
  97199. insights
  97200. cycloadd
  97201. theory
  97202. reactive
  97203. intermediates
  97204. reaction
  97205. mecha
  97206. kendall
  97207. evanseck
  97208. jeffrey
  97209. transiton
  97210. structures
  97211. houlihan
  97212. hoult
  97213. houlton
  97214. houlton
  97215. sarah
  97216. fk506
  97217. organ
  97218. transplants
  97219. chemistry
  97220. hounsell
  97221. house
  97222. housecroft
  97223. houshang
  97224. hoveyda
  97225. hoveyda
  97226. evans
  97227. david
  97228. gregory
  97229. substrate
  97230. directab
  97231. common
  97232. base-initiated
  97233. concerted
  97234. 12-eliminations
  97235. chiral
  97236. salen
  97237. manganese
  97238. complex
  97239. discriminate
  97240. combination
  97241. group
  97242. sulfonyl
  97243. radicals
  97244. nature
  97245. synthesizes
  97246. vitamin
  97247. survey
  97248. howard
  97249. howarth
  97250. howarth
  97251. lilley
  97252. carbon
  97253. peptides
  97254. prote
  97255. howell
  97256. howells
  97257. shmaryahu
  97258. transition
  97259. state
  97260. indeed
  97261. intermediate
  97262. shmaryhau
  97263. traditional
  97264. interpretation
  97265. hptlc
  97266. hsiung
  97267. chiral
  97268. sulfinylallyl
  97269. sulfinyl
  97270. ketimine
  97271. anion
  97272. huang
  97273. huang
  97274. weiyuan
  97275. perfluoroalkylation
  97276. initiated
  97277. sodium
  97278. huang
  97279. yaozeng
  97280. synthetic
  97281. applications
  97282. organoantimony
  97283. compo
  97284. huang
  97285. zhitang
  97286. meixiang
  97287. heterocyclic
  97288. ketene
  97289. aminals
  97290. hubert
  97291. huche
  97292. huche
  97293. alpha
  97294. aiienic
  97295. ketones
  97296. french
  97297. tetrahed
  97298. huckel
  97299. hudlicky
  97300. hudlicky
  97301. intramolecular
  97302. nucleophilic
  97303. displacement
  97304. fluor
  97305. hudlicky
  97306. enantioselective
  97307. synthesis
  97308. alkaloids
  97309. carbo
  97310. hudlicky
  97311. tomas
  97312. cebulak
  97313. cyclitols
  97314. their
  97315. derivatives
  97316. hudlicky
  97317. tomas
  97318. rulin
  97319. hector
  97320. olivo
  97321. horacio
  97322. price
  97323. hudlicky
  97324. tomas
  97325. rulin
  97326. josephine
  97327. gadamasetti
  97328. kumar
  97329. hudlicky
  97330. tomas
  97331. seoane
  97332. gustavo
  97333. price
  97334. gadamasetti
  97335. kumar
  97336. hudrlik
  97337. hudrlik
  97338. hudrlik
  97339. epoxysilanes
  97340. advances
  97341. hudson
  97342. huenig
  97343. huffmant
  97344. hughes
  97345. hughes
  97346. recent
  97347. developments
  97348. phosphole
  97349. phosphindole
  97350. hughes
  97351. synthetic
  97352. applications
  97353. dimethyl
  97354. acetylenedicar
  97355. hughes
  97356. maclean
  97357. spectra
  97358. isoquinoline
  97359. hughes
  97360. david
  97361. progress
  97362. fischer
  97363. indole
  97364. reaction
  97365. organ
  97366. hughes
  97367. david
  97368. mitsunobu
  97369. reaction
  97370. 42335
  97371. organic
  97372. hughes
  97373. ricco
  97374. butler
  97375. martin
  97376. chemical
  97377. microsen
  97378. huiping
  97379. huisgen
  97380. huisgen
  97381. electrocyclizations
  97382. important
  97383. principle
  97384. huisgen
  97385. adventure
  97386. playground
  97387. review
  97388. huisman
  97389. hulce
  97390. hulliger
  97391. hulliger
  97392. juerg
  97393. chemistry
  97394. crystal
  97395. growth
  97396. angewandte
  97397. chemi
  97398. hulshof
  97399. hulshof
  97400. wynberg
  97401. vanishing
  97402. optical
  97403. activity
  97404. norin
  97405. torbjoern
  97406. enantioselectivity
  97407. lipases
  97408. human
  97409. humana
  97410. humphries
  97411. hund's
  97412. hundred
  97413. hungary
  97414. hunger
  97415. hunig
  97416. hunig
  97417. berneth
  97418. reversible
  97419. redox
  97420. systems
  97421. hunsdiecker
  97422. hunter
  97423. hunter
  97424. christopher
  97425. arene
  97426. arene
  97427. interactions
  97428. electrostatic
  97429. hunter
  97430. christopher
  97431. aromatic
  97432. interactions
  97433. hunter
  97434. stothers
  97435. warnhoff
  97436. rearrangements
  97437. carba
  97438. hunteria
  97439. huperazine
  97440. huperzine-a
  97441. huperzine-a
  97442. possible
  97443. tructure
  97444. treatment
  97445. hurdlik
  97446. hurley
  97447. hurley
  97448. biosynthetic
  97449. pathways
  97450. leading
  97451. pyrrolo
  97452. hurstg
  97453. hurst
  97454. cyclobutanes
  97455. second
  97456. supplements
  97457. hurst
  97458. cyclopentanes
  97459. second
  97460. supplements
  97461. hurst
  97462. derek
  97463. nitration
  97464. phenyl
  97465. substituted
  97466. heterocycl
  97467. hussein
  97468. hussey
  97469. hutchings
  97470. hutchings
  97471. graham
  97472. catalysis
  97473. intracrystalline
  97474. space
  97475. hutchins
  97476. hutchins
  97477. cistone
  97478. utility
  97479. applications
  97480. borane
  97481. hutchinson
  97482. hutchinson
  97483. camptothecin
  97484. chemistry
  97485. biogenesis
  97486. medicin
  97487. huthig
  97488. hutton
  97489. huybrechts
  97490. huyser
  97491. hybrid
  97492. hybrid
  97493. enzymes
  97494. sequence-specific
  97495. cleavage
  97496. nucleic
  97497. hybridization
  97498. hydra
  97499. hydrated
  97500. hydrates
  97501. hydration
  97502. hydration
  97503. olefins
  97504. dienes
  97505. acetylenes
  97506. hydroboration
  97507. hydrazi
  97508. hydrazides
  97509. hydrazidoyl
  97510. hydrazine
  97511. hydrazine
  97512. synthetic
  97513. hydrazine
  97514. rocket
  97515. synthetic
  97516. hydrazines
  97517. hydrazines
  97518. hydrazinium
  97519. hydrazino
  97520. hydrazinopyrimidines
  97521. hydrazo
  97522. hydrazonates
  97523. hydrazone
  97524. hydrazone
  97525. anions
  97526. hydrazones
  97527. hydrazonium
  97528. hydrazonium
  97529. salts
  97530. hydrazonyl
  97531. hydride
  97532. hydride
  97533. shifts
  97534. transfers
  97535. hydrido
  97536. hydrindan
  97537. hydrindenone
  97538. hydro
  97539. hydroalkenylation
  97540. hydroalumination
  97541. hydroalumination
  97542. alkynes
  97543. hydroamination
  97544. hydroaromatic
  97545. hydroarylation
  97546. hydroazulene
  97547. hydroazulenes
  97548. hydroboraing
  97549. hydroborating
  97550. hydroboration
  97551. improved
  97552. procedure
  97553. synthesis
  97554. hydroboration
  97555. alkynes
  97556. hydroboration/intram
  97557. hydroboration/intram
  97558. reduction
  97559. allyl
  97560. ketones
  97561. diisopi
  97562. hydroborations
  97563. hydrocarbon
  97564. hydrocarbon
  97565. radical
  97566. cations
  97567. hydrocarbonation
  97568. hydrocarbonsR
  97569. hydrocarbons
  97570. hydrocarbonylation
  97571. hydrocarboxylation
  97572. hydrocarbyls
  97573. hydrochlorination
  97574. hydrocyanation
  97575. hydrocyanation
  97576. conjugate
  97577. carbonyl
  97578. compounds
  97579. hydrofolic
  97580. hydroformylation
  97581. formylation
  97582. related
  97583. additions
  97584. carbon
  97585. monoxide
  97586. hydroformylation
  97587. catalyzed
  97588. ruthenium
  97589. complexes
  97590. hydrogen
  97591. hydrogen
  97592. hydrogen
  97593. transfer
  97594. reactions
  97595. trimethylenemethane
  97596. hydrogen
  97597. bonding
  97598. chemical
  97599. reactivity
  97600. hydrogen
  97601. bonding
  97602. stereocontrolling
  97603. element
  97604. hydrogen-active
  97605. hydrogen-atom
  97606. hydrogen-bonded
  97607. hydrogenated
  97608. hydrogenated
  97609. porphyrin
  97610. derivatives
  97611. hydroporphyrins
  97612. hydrogenation
  97613. drogenations
  97614. hydrogenations
  97615. hydrogenolysable
  97616. hydrogenolysis
  97617. hydrogenolysis
  97618. allyl
  97619. benzyl
  97620. halides
  97621. related
  97622. compo
  97623. hydrogenolysis
  97624. benzyl
  97625. groups
  97626. attached
  97627. oxygen
  97628. nitrogen
  97629. hydrogenolytic
  97630. hydroisoquinoline
  97631. hydroisoquinoline
  97632. construction
  97633. diels
  97634. alder
  97635. hydrolase
  97636. hydrolases
  97637. hydrolases
  97638. organic
  97639. synthesis
  97640. preparation
  97641. enantiomerica
  97642. hydrolysis
  97643. hydrolysis
  97644. other
  97645. cleavages
  97646. glycosidic
  97647. linkages
  97648. hydrolysis
  97649. acetals
  97650. ketals
  97651. position
  97652. transition
  97653. hydrolysis
  97654. orthocarbonates
  97655. evidence
  97656. charge
  97657. imbalance
  97658. hydrolytic
  97659. hydrolyzable
  97660. hydromagnesiation
  97661. hydrometallation
  97662. hydrooxygenation
  97663. hydroperoxide
  97664. hydroperoxides
  97665. hydroperoxides
  97666. hydroperoxyethyl
  97667. hydrophenylation
  97668. hydrophobic
  97669. hydrophobic
  97670. effects
  97671. simple
  97672. organic
  97673. reactions
  97674. water
  97675. hydroporphyrins
  97676. hydroproxides
  97677. hydroquinones
  97678. hydrosilame
  97679. hydrosilane
  97680. hydrosilanes
  97681. hydrosilation
  97682. hydrosilylation
  97683. alkynes
  97684. hydrosilylation
  97685. enones
  97686. platinum
  97687. divinyltetramethyldi
  97688. hydrosulfonation
  97689. hydrothermal
  97690. hydrovinylation
  97691. hydroxamate
  97692. hydroxamates
  97693. hydroxamic
  97694. hydroxide
  97695. hydroximic
  97696. hydroximoyl
  97697. hydroxo
  97698. hydroxy
  97699. hydroxy
  97700. hydroxy
  97701. directed
  97702. ketone
  97703. reduction
  97704. application
  97705. synthes
  97706. hydroxy
  97707. organosulfonyloxy
  97708. arenes
  97709. organic
  97710. synthesis
  97711. hydroxy
  97712. tosyloxy
  97713. benzene
  97714. useful
  97715. hypervalent
  97716. iodine
  97717. hydroxy-directed
  97718. hydroxy-epoxidation
  97719. hydroxyacid
  97720. hydroxyacids
  97721. hydroxyacyl
  97722. hydroxyalkyl
  97723. hydroxyalkynes
  97724. hydroxyamidines
  97725. hydroxyaminoacids
  97726. hydroxyarenes
  97727. hydroxyaryl
  97728. hydroxybenzoic
  97729. hydroxybornanes
  97730. hydroxybutanals
  97731. hydroxybutanoates
  97732. hydroxycarbazoles
  97733. hydroxychromones
  97734. hydroxycinnamic
  97735. hydroxycodeine
  97736. hydroxycyclobutenone
  97737. xyethylene
  97738. hydroxyindoles
  97739. hydroxyketones
  97740. hydroxyl
  97741. hydroxyl
  97742. directed
  97743. stereoselective
  97744. sigmatropic
  97745. rearrangeme
  97746. hydroxyl-directed
  97747. hydroxylamine
  97748. hydroxylamine
  97749. sulfonic
  97750. versatile
  97751. synthetic
  97752. reagent
  97753. hydroxylamine-o-sulf
  97754. hydroxylamine-o-sulf
  97755. hydroxylamines
  97756. hydroxylamino
  97757. hydroxylases
  97758. hydroxylated
  97759. hydroxylation
  97760. hydroxylations
  97761. hydroxylatyion
  97762. hydroxylatyion
  97763. aromatic
  97764. compounds
  97765. nitrous
  97766. oxide
  97767. hydroxymethyl
  97768. hydroxymethylcyclopr
  97769. hydroxymethylidene
  97770. hydroxymorphine
  97771. hydroxyprolines
  97772. hydroxypyrazoline
  97773. hydroxypyrroles
  97774. hydroxystannanes
  97775. hydroxytetrahydrofur
  97776. hydroxytetrahydropyr
  97777. hydrozirconation
  97778. hydrozirconation
  97779. transition
  97780. metal
  97781. reagent
  97782. organic
  97783. hydrozirconation
  97784. alkynes
  97785. hydrometallation
  97786. hydrozirconation-iso
  97787. hydrozirconation-iso
  97788. reactions
  97789. terminally
  97790. functionalized
  97791. hyean
  97792. hygromycin-a
  97793. hyperbranched
  97794. hypercarbon
  97795. hypercarbon
  97796. chemistry
  97797. hyperconjugation
  97798. hypercoordinate
  97799. hypersensitive
  97800. hypervalent
  97801. hypervalent
  97802. alkyliodine
  97803. chemistry
  97804. hypervalent
  97805. iodine
  97806. organic
  97807. synthesis
  97808. hypervalent
  97809. iodine
  97810. induced
  97811. nucleophilic
  97812. substitution
  97813. hypervalent
  97814. iodine
  97815. oxidation
  97816. methyl
  97817. quinolones
  97818. using
  97819. hypervalent
  97820. iodine
  97821. reagents
  97822. synthesis
  97823. heterocyclic
  97824. hypervalentalkyliodi
  97825. hypochlorite
  97826. hypochlorites
  97827. hypofluorites
  97828. hypofluorites
  97829. their
  97830. application
  97831. organic
  97832. synthesis
  97833. hypohalite
  97834. hypohalites
  97835. hypoiodite
  97836. hypolipidemic
  97837. hypophosphites
  97838. hypotensive
  97839. hypothetical
  97840. hysteresis
  97841. hyushin
  97842. smith
  97843. deuterium
  97844. aldrichimica
  97845. ernest
  97846. angew
  97847. synthesis
  97848. prosta
  97849. fleming
  97850. frontier
  97851. orbitals
  97852. organic
  97853. chemical
  97854. reactions
  97855. hermecz
  97856. vasuari
  97857. debreczy
  97858. heterocycl
  97859. kitagawa
  97860. yoshikawa
  97861. selective
  97862. cleavage
  97863. glucuronide
  97864. kuwajima
  97865. nakamura
  97866. reactive
  97867. kuwajima
  97868. nakamura
  97869. reactive
  97870. karle
  97871. molecular
  97872. formula
  97873. configuration
  97874. conformation
  97875. knuynants
  97876. polishchuk
  97877. lockhart
  97878. chromanols
  97879. chromanones
  97880. chromenes
  97881. chroma
  97882. minale
  97883. cimino
  97884. stefano
  97885. sodano
  97886. natural
  97887. products
  97888. beletskaya
  97889. artamkina
  97890. reutov
  97891. beletskaya
  97892. artamkina
  97893. reutov
  97894. paterson
  97895. mansuri
  97896. tetrahedron
  97897. recent
  97898. saito
  97899. matsuura
  97900. tetrahedron
  97901. recent
  97902. aspec
  97903. saito
  97904. matsuura
  97905. nakagawa
  97906. peroxidic
  97907. intermedi
  97908. schmeltz
  97909. hoffmann
  97910. nitrogen
  97911. containing
  97912. compounds
  97913. fleming
  97914. frontier
  97915. orbitals
  97916. organic
  97917. chemical
  97918. reactions
  97919. i-prli@
  97920. iddon
  97921. brian
  97922. synthesis
  97923. reactions
  97924. lithiated
  97925. monocyclic
  97926. illuminati
  97927. mandolini
  97928. closure
  97929. reactions
  97930. bifunctio@
  97931. imidazolin-4-ones@
  97932. imidines@
  97933. iminophosphines
  97934. unconventional
  97935. compounds
  97936. group
  97937. eleme@
  97938. importance
  97939. importance
  97940. heterocycles
  97941. biochemical
  97942. pathways@
  97943. industrial
  97944. aspects
  97945. selectivity
  97946. applying
  97947. homogeneous
  97948. catal@
  97949. infrared
  97950. innovation
  97951. insecticide
  97952. interaction
  97953. interconversion
  97954. nonracemic
  97955. a-otbs
  97956. crotyl
  97957. g-otbs
  97958. metha@
  97959. intermediates
  97960. international
  97961. interrelations
  97962. among
  97963. peri-condensed
  97964. thiophenes
  97965. i2-promoted
  97966. i2-promoted
  97967. palladium
  97968. catalyzed
  97969. carbonylation
  97970. amines
  97971. iacobucci
  97972. fleming
  97973. elements
  97974. organi
  97975. ibophyllidine
  97976. ibragimov
  97977. ibrahim
  97978. ibuak
  97979. ibuka
  97980. icals
  97981. icarbonylcyclopentad
  97982. ication
  97983. ichihara
  97984. ichikawa
  97985. ichikawa
  97986. tsuneki
  97987. application
  97988. spectroscopy
  97989. ichimnru
  97990. ichiro
  97991. ichiya
  97992. idacavage
  97993. iddon
  97994. iddon
  97995. scriven
  97996. suschitzky
  97997. gallagher
  97998. iddon
  97999. ngochindo
  98000. synthesis
  98001. reactions
  98002. lithiated
  98003. iddon
  98004. recent
  98005. advances
  98006. synthesis
  98007. benzo
  98008. thiophen
  98009. iddon
  98010. brian
  98011. synthesis
  98012. reactions
  98013. lithiated
  98014. monocyclic
  98015. ideal
  98016. ideas
  98017. identification
  98018. identifying
  98019. noble
  98020. carbanions
  98021. reactive
  98022. intermediates
  98023. jones
  98024. ieaving
  98025. iedda
  98026. igarashi
  98027. igersheim
  98028. pressure
  98029. chemical
  98030. synthesis
  98031. ignat'eva
  98032. ignatova
  98033. ignatovich
  98034. ihara
  98035. ihlenfeldt
  98036. iintoku
  98037. weinstein
  98038. ravid
  98039. synthesis
  98040. saturated
  98041. gamma
  98042. raphael
  98043. natural
  98044. products
  98045. laboratory
  98046. guide
  98047. ikarugamycin
  98048. ikchoon
  98049. ikeda
  98050. ikeda
  98051. tamura
  98052. haloindolenines
  98053. versatile
  98054. intermediates
  98055. ikegami
  98056. ikehara
  98057. ikehara
  98058. ohtsuka
  98059. markham
  98060. synthesis
  98061. polynucleot
  98062. ikekawa
  98063. ikekawa
  98064. nobuo
  98065. morisaki
  98066. masuo
  98067. fujimoto
  98068. yoshi
  98069. sterol
  98070. ikuro
  98071. ikuya
  98072. il'chenko
  98073. ilane
  98074. sinkovic
  98075. trinajstic
  98076. topological
  98077. resonance
  98078. energie
  98079. illinois
  98080. illudin
  98081. illudins
  98082. illudol
  98083. illuminati
  98084. illuminati
  98085. mandolini
  98086. closure
  98087. reactions
  98088. bifunctio
  98089. illusion
  98090. ilsley
  98091. ilylenes
  98092. imaging
  98093. imamoto
  98094. imamoto
  98095. tsuneo
  98096. synthesis
  98097. reactions
  98098. phosphine
  98099. imashev
  98100. imbalance
  98101. imboden
  98102. imerubrine
  98103. imidate
  98104. imidates
  98105. imidazo
  98106. imidazole
  98107. imidazole-2-thiones
  98108. imidazole-2-thiones
  98109. synthesis
  98110. structure
  98111. properties
  98112. imidazoles
  98113. imidazoles
  98114. their
  98115. benzo
  98116. derivatives
  98117. structure
  98118. imidazoles
  98119. their
  98120. benzo
  98121. derivatives
  98122. reactivity
  98123. imidazoles
  98124. their
  98125. benzo
  98126. derivatives
  98127. synthesis
  98128. imidazolidium
  98129. imidazolyl
  98130. imidazolyloxazolones
  98131. imidazopyrimidines
  98132. imidchloride
  98133. imide
  98134. imides
  98135. imidic
  98136. imidines
  98137. imidophosphorus
  98138. imidotitanium-alkyne
  98139. imidoyl
  98140. imidoyl
  98141. alides
  98142. hydroxamic
  98143. halides
  98144. hydrazonyl
  98145. halides
  98146. imidoylstannanes
  98147. imine
  98148. imine-forming
  98149. imines
  98150. iminium
  98151. imino
  98152. imino-12-thiazedine
  98153. imino-functionalized
  98154. iminoacyl
  98155. iminoboranes
  98156. iminocarboxylic
  98157. iminoformylation
  98158. iminomethylene
  98159. iminophosphanes
  98160. iminophosphines
  98161. iminophosphines
  98162. unconventional
  98163. compounds
  98164. group
  98165. eleme
  98166. iminophosphoranes
  98167. iminophosphoranes
  98168. useful
  98169. building-blocks
  98170. preparation
  98171. iminophosphoranylide
  98172. iminyl
  98173. iminyl
  98174. radicals
  98175. stannane
  98176. mediated
  98177. cleavage
  98178. oxime
  98179. ester
  98180. immacolata
  98181. immanuel
  98182. immines
  98183. imming
  98184. immobilized
  98185. immobilizing
  98186. immune
  98187. immunoassay
  98188. immunoassay
  98189. alkaloids
  98190. immunoassays
  98191. immunochemistry
  98192. immunology
  98193. immunomodulant
  98194. immunomodulators
  98195. immunomodulators-syn
  98196. immunophilin
  98197. immunophilin-ligand
  98198. immunophilins
  98199. immunostimulants
  98200. immunosuppresive
  98201. immunosuppressant
  98202. immunosuppressive
  98203. immunotropic
  98204. impact
  98205. implementation
  98206. implic
  98207. implications
  98208. importance
  98209. importance
  98210. tance
  98211. heterocycles
  98212. biochemical
  98213. pathways
  98214. important
  98215. imposed
  98216. imprinting
  98217. improved
  98218. improved
  98219. alkylation
  98220. ethyl
  98221. acetoacetate
  98222. diethyl
  98223. malona
  98224. improved
  98225. amination
  98226. ethyl
  98227. nitrophenyl
  98228. sulfonyl
  98229. oxycar
  98230. improved
  98231. method
  98232. preparation
  98233. guanidines
  98234. improved
  98235. methods
  98236. synthesis
  98237. aza-crown
  98238. macrocycles
  98239. improvements
  98240. improvements
  98241. synthesis
  98242. trehalose-based
  98243. bacterial
  98244. impurities
  98245. included
  98246. includes
  98247. includes
  98248. including
  98249. incluhion
  98250. inclusion
  98251. inclusion
  98252. complexes
  98253. cyclomalto-oligosacc
  98254. cyclodextrin
  98255. incorporated
  98256. incorporating
  98257. incorporation
  98258. increase
  98259. increased
  98260. increasing
  98261. incycloproparene
  98262. lizines
  98263. indacene
  98264. indacenes
  98265. indanes
  98266. indanomycin
  98267. indanones
  98268. indazol
  98269. indazole
  98270. indazoles
  98271. indazoles
  98272. benzopyrazoles
  98273. indeed
  98274. indene
  98275. indenides
  98276. indeno
  98277. indenone
  98278. indenone
  98279. synthesis
  98280. improved
  98281. synthetic
  98282. protocol
  98283. effect
  98284. indenones
  98285. indenyl
  98286. indenyl
  98287. cobalt
  98288. catalyzed
  98289. cocyclization
  98290. alkyne
  98291. alkene
  98292. index
  98293. india
  98294. indian
  98295. indirect
  98296. indirect
  98297. electroorganic
  98298. synthesis
  98299. modern
  98300. chapter
  98301. organi
  98302. indispensable
  98303. indium
  98304. indoies
  98305. indol
  98306. indol
  98307. tributylstannane
  98308. versatile
  98309. reagent
  98310. substi
  98311. indol
  98312. yltributylstannane
  98313. versatile
  98314. reagent
  98315. substit
  98316. indolactam
  98317. indole
  98318. indoles
  98319. indolethiols
  98320. indolic
  98321. indolin
  98322. indolin-2
  98323. indolization
  98324. indolizidin
  98325. indolizidine
  98326. indolizidine
  98327. quinolizidine
  98328. alkaloids
  98329. indolizidines
  98330. indolizine
  98331. indolizomycin
  98332. indolo
  98333. indolo-23-quinodimet
  98334. indolo-23-quinodimet
  98335. stable
  98336. cyclic
  98337. analogs
  98338. regio
  98339. indolones
  98340. indolopyridoimidazol
  98341. indoloquinones
  98342. indolyl
  98343. indolylmethyl
  98344. indoxazenes
  98345. induce
  98346. inducedq
  98347. induced
  98348. induced
  98349. optical
  98350. activity
  98351. cyclodextrin
  98352. complexes
  98353. inducing
  98354. inductio
  98355. induction
  98356. inductive
  98357. enhancement
  98358. neighboring
  98359. group
  98360. participation
  98361. inductivity
  98362. inductivity
  98363. bridging
  98364. carbocations
  98365. industrial
  98366. industrial
  98367. applications
  98368. wittig
  98369. reaction
  98370. industrial
  98371. aspects
  98372. selectivity
  98373. applying
  98374. homogeneous
  98375. catal
  98376. industrial
  98377. synthesis
  98378. optically
  98379. active
  98380. compounds
  98381. industrial
  98382. synthesis
  98383. terpene
  98384. compounds
  98385. industrial
  98386. transformations
  98387. penicillins
  98388. cephalosporins
  98389. industryS
  98390. inent
  98391. inept
  98392. inexpensive
  98393. infancy
  98394. infection
  98395. infectives
  98396. inferred
  98397. infinity
  98398. inflammation
  98399. inflammatory
  98400. influence
  98401. influence
  98402. tributyltin
  98403. oxide
  98404. aminyl
  98405. radical
  98406. cycliza
  98407. influences
  98408. influencing
  98409. influenza
  98410. information
  98411. infraredL
  98412. infrared
  98413. infuences
  98414. ingeborg
  98415. ingenane
  98416. ingersoll
  98417. ingham
  98418. ingold
  98419. ingredients
  98420. ingrid
  98421. inhibiting
  98422. inhibition
  98423. inhibitor
  98424. inhibitors
  98425. inhibitory
  98426. initial
  98427. initiate
  98428. initiated
  98429. initiating
  98430. initiation
  98431. initiator
  98432. initiators
  98433. initio
  98434. inner
  98435. inner-sphere
  98436. inner-sphere
  98437. electron
  98438. transfer
  98439. organic
  98440. chemistry
  98441. relevanc
  98442. innocent
  98443. innovation
  98444. innovation
  98445. inoguchi
  98446. inoguchi
  98447. kiyoshi
  98448. sakuraba
  98449. shunji
  98450. achiwa
  98451. kazuo
  98452. design
  98453. concept
  98454. inokawa
  98455. inokuchi
  98456. inorganic
  98457. inorganic
  98458. derivatives
  98459. inorganic
  98460. halogen
  98461. compounds
  98462. oxidation
  98463. reagents
  98464. inorganic
  98465. nitrogen
  98466. compounds
  98467. oxidation
  98468. reagents
  98469. inorganic
  98470. phosphorus
  98471. arsenic
  98472. antimony
  98473. bismuth
  98474. compounds
  98475. inorganic
  98476. sulfur
  98477. compounds
  98478. oxidation
  98479. reagents
  98480. inosine
  98481. inositol
  98482. inositols
  98483. inoue
  98484. inoue
  98485. yoshihisa
  98486. asymmetric
  98487. photochemical
  98488. reactions
  98489. soluti
  98490. inouye
  98491. inpursuit
  98492. insect
  98493. insect
  98494. antifeedants
  98495. insect
  98496. pheromones
  98497. related
  98498. natural
  98499. products
  98500. insect
  98501. semiochemicals
  98502. insecticide
  98503. insecticide
  98504. insecticides
  98505. insects
  98506. inserted
  98507. insertion
  98508. rbenoid
  98509. fe2p2
  98510. cluster
  98511. insertionof
  98512. insertions
  98513. inside
  98514. inside-outside
  98515. inside-outside
  98516. stereisomerization
  98517. synthesis
  98518. trans-bicyc
  98519. insight
  98520. insights
  98521. insights
  98522. mechanism
  98523. cleavage
  98524. dynemicin
  98525. insoluble
  98526. insolution
  98527. instant
  98528. institutes
  98529. instrumentation
  98530. insulating
  98531. integrated
  98532. intelligent
  98533. intensely
  98534. intensities
  98535. intensity
  98536. interact
  98537. interaction
  98538. interaction
  98539. interaction
  98540. calicheamicin
  98541. duplex
  98542. interaction
  98543. orbitals
  98544. through
  98545. space
  98546. through
  98547. bonds
  98548. interaction
  98549. organometallic
  98550. moieties
  98551. carbanions
  98552. interactions
  98553. interactions
  98554. between
  98555. nonconjugated
  98556. systems
  98557. interactions
  98558. ketenes
  98559. organometallic
  98560. compounds
  98561. ketene
  98562. interactive
  98563. intercalated
  98564. intercalation
  98565. intercalation
  98566. compounds
  98567. alkali
  98568. metals
  98569. graphite
  98570. intercepted
  98571. interception
  98572. interchange
  98573. interconversion
  98574. interconversion
  98575. nonracemic
  98576. a-otbs
  98577. crotyl
  98578. g-otbs
  98579. metha
  98580. interconversions
  98581. interconversions
  98582. among
  98583. trimethylsilyl
  98584. alkoxides
  98585. trimethy
  98586. interdisciplinary
  98587. interest
  98588. interesting
  98589. interface
  98590. interfaces
  98591. interim
  98592. interlacing
  98593. interlacing
  98594. molecular
  98595. threads
  98596. transition
  98597. metals
  98598. catenands
  98599. interligand
  98600. interlocked
  98601. interlocking
  98602. intermedi
  98603. intermediacy
  98604. intermediaires
  98605. intermediary
  98606. intermediate
  98607. intermediates
  98608. intermediates
  98609. intermediates
  98610. reaction
  98611. mechanisms
  98612. interaction
  98613. intermolecular
  98614. cycloadditions
  98615. intermolecular
  98616. intramolecular
  98617. diels-alder
  98618. reactions
  98619. intermolecular
  98620. intramolecular
  98621. hetero
  98622. diels
  98623. alder
  98624. reactio
  98625. intermolecular
  98626. diels-alder
  98627. reactions
  98628. internal
  98629. internationai
  98630. international
  98631. international
  98632. international
  98633. interplay
  98634. interplay
  98635. theory
  98636. experiment
  98637. determination
  98638. interpretationL
  98639. interpreting
  98640. interrelations
  98641. interrelations
  98642. among
  98643. peri-condensed
  98644. thiophenes
  98645. interrelations
  98646. chemistry
  98647. biotechnology
  98648. biotransform
  98649. interrelationships
  98650. interscience
  98651. interstellar
  98652. intersystem
  98653. intersystem
  98654. crossing
  98655. triplet
  98656. biradicals
  98657. conformational
  98658. intervention
  98659. intoD
  98660. ntrabridgehead
  98661. intrabridgehead
  98662. chemistry
  98663. intracellular
  98664. intracellular
  98665. steps
  98666. bacterial
  98667. peptidoglycan
  98668. intracrystalline
  98669. intramolcular
  98670. intramolcular
  98671. reactions
  98672. fischer
  98673. carbene
  98674. complexes
  98675. intramolecular
  98676. intersystem
  98677. crossing
  98678. triplet
  98679. biradicals
  98680. conformational@
  98681. intr@
  98682. intramolecular
  98683. intramolecular
  98684. 13-dipolar
  98685. cycloaddition
  98686. chemistry@
  98687. intramolecular
  98688. photoaddition
  98689. cyclobutane
  98690. fragmentation
  98691. intramolecular
  98692. cyclization
  98693. a-lithioamine
  98694. synthetic
  98695. equiva@
  98696. intramolecular
  98697. diels
  98698. alder
  98699. reactions
  98700. recent
  98701. advances
  98702. intramolecular
  98703. hydroxycyclopropanat
  98704. w-vinyl
  98705. carboxylic
  98706. intramolecular
  98707. michael
  98708. additions
  98709. review@
  98710. intramolecular
  98711. reactions
  98712. n-acyliminium
  98713. intermediates@
  98714. intramolecular
  98715. schmidt
  98716. reactions
  98717. azides
  98718. carbocations@
  98719. isoquinoline
  98720. isotope
  98721. istry@
  98722. iwamura
  98723. sarma
  98724. sharma
  98725. heterocycles
  98726. synthesis
  98727. mills
  98728. maryanoff
  98729. eisch
  98730. rearrangement
  98731. unsaturated
  98732. organoboron
  98733. organ@
  98734. intramolecular
  98735. intramolecular
  98736. intramolecular
  98737. 13-dipolar
  98738. cycloaddition
  98739. reactions
  98740. intramolecular
  98741. 13-dipolar
  98742. cycloadditions
  98743. intramolecular
  98744. hydride
  98745. transfer
  98746. acyclic
  98747. diols
  98748. intramolecular
  98749. photoaddition
  98750. cyclobutane
  98751. fragmentation
  98752. intramolecular
  98753. photocycloaddition
  98754. vinylarenes
  98755. synthes
  98756. intramolecular
  98757. cycloadditions
  98758. organic
  98759. synthes
  98760. intramolecular
  98761. cycloaddition
  98762. reactions
  98763. pyridazino
  98764. intramolecular
  98765. cycloadditions
  98766. oxallyl
  98767. cations
  98768. intramolecular
  98769. addition
  98770. reactions
  98771. allylic
  98772. propargylic
  98773. intramolecular
  98774. alkoxycarbonylation
  98775. hydroxy
  98776. alkenes
  98777. promot
  98778. intramolecular
  98779. alkylation
  98780. carboxylic
  98781. acids
  98782. application
  98783. intramolecular
  98784. allylsilane
  98785. addition
  98786. chiral
  98787. alkylidene-13-
  98788. intramolecular
  98789. allylstannane-aldehy
  98790. cyclizations
  98791. stereochemi
  98792. intramolecular
  98793. amination
  98794. olefins
  98795. synthesis
  98796. substitut
  98797. intramolecular
  98798. anodic
  98799. olefin
  98800. coupling
  98801. reactions
  98802. intramolecular
  98803. bicyclizations
  98804. tosylamide-containin
  98805. alkyny
  98806. intramolecular
  98807. conjugate
  98808. addition
  98809. allylic
  98810. trichloroacetim
  98811. intramolecular
  98812. coordination
  98813. organotin
  98814. chemistry
  98815. intramolecular
  98816. cyclization
  98817. a-lithioamine
  98818. synthetic
  98819. equiva
  98820. intramolecular
  98821. cyclization
  98822. alkenes
  98823. alkynes
  98824. promoted
  98825. intramolecular
  98826. cyclization
  98827. ortho
  98828. iodophenyl
  98829. butenoate
  98830. intramolecular
  98831. cyclization
  98832. phenyl
  98833. benzothiophenium
  98834. intramolecular
  98835. cyclizations
  98836. ring-cleavage
  98837. reactions
  98838. intramolecular
  98839. cycloaddition
  98840. azides
  98841. electron
  98842. intramolecular
  98843. cycloaddition
  98844. reactions
  98845. dienyl
  98846. nitroso
  98847. intramolecular
  98848. cycloaddition
  98849. reactions
  98850. ortho
  98851. quinodimetha
  98852. intramolecular
  98853. cycloadditions
  98854. ketenes
  98855. keteniminium
  98856. intramolecular
  98857. diels
  98858. alder
  98859. adducts
  98860. dithiolium
  98861. salts
  98862. intramolecular
  98863. diels
  98864. alder
  98865. furans
  98866. intramolecular
  98867. diels
  98868. alder
  98869. reaction
  98870. azanonatrienes
  98871. intramolecular
  98872. diels
  98873. alder
  98874. reaction
  98875. furans
  98876. related
  98877. intramolecular
  98878. diels
  98879. alder
  98880. reaction
  98881. furans
  98882. allenylet
  98883. intramolecular
  98884. diels
  98885. alder
  98886. reactions
  98887. intramolecular
  98888. diels
  98889. alder
  98890. reactions
  98891. recent
  98892. advances
  98893. intramolecular
  98894. diels
  98895. alder
  98896. reactions
  98897. sulfone
  98898. substituted
  98899. intramolecular
  98900. diels
  98901. alder
  98902. route
  98903. oxodecahydroisoquino
  98904. intramolecular
  98905. diels-alder
  98906. reactions
  98907. intramolecular
  98908. diels-alder
  98909. reactions
  98910. intramolecular
  98911. trapping
  98912. chemistry
  98913. decoupling
  98914. intramolecular
  98915. reaction
  98916. olefin
  98917. aldehydes
  98918. intramolecular
  98919. reactions
  98920. organic
  98921. synthesis
  98922. intramolecular
  98923. radical
  98924. reaction
  98925. intramolecular
  98926. hetero-diels-alder
  98927. reaction
  98928. prolinol-deriv
  98929. intramolecular
  98930. homolytic
  98931. displacements
  98932. polar
  98933. effects
  98934. intramolecular
  98935. homolytic
  98936. substitutions
  98937. influence
  98938. intramolecular
  98939. horner
  98940. wadsworth
  98941. emmons
  98942. reaction
  98943. intramolecular
  98944. initiated
  98945. cyclization
  98946. acyliminium
  98947. salts
  98948. intramolecular
  98949. interactions
  98950. between
  98951. sulfur
  98952. atoms
  98953. cyclotet
  98954. intramolecular
  98955. michael
  98956. additions
  98957. copper
  98958. chloride-mediated
  98959. intramolecular
  98960. michael
  98961. additions
  98962. review
  98963. intramolecular
  98964. michael
  98965. michael
  98966. additions
  98967. carbon
  98968. intramolecular
  98969. michael
  98970. anti-michael
  98971. additions
  98972. carbon-
  98973. intramolecular
  98974. nitrile
  98975. imine
  98976. cycloadditions
  98977. acetyleni
  98978. intramolecular
  98979. nucleophilic
  98980. substitution
  98981. reactions
  98982. intramolecular
  98983. nucleophilic
  98984. substitution
  98985. reactions
  98986. intramolecular
  98987. oxidative
  98988. cyclisation
  98989. alcohols
  98990. intramolecular
  98991. pericyclic
  98992. reactions
  98993. acetylenic
  98994. compounds
  98995. intramolecular
  98996. pericyclic
  98997. reactions
  98998. cetylenic
  98999. compounds
  99000. intramolecular
  99001. photoaddition
  99002. terminal
  99003. allenes
  99004. conjugat
  99005. intramolecular
  99006. photochemical
  99007. cycloadditions
  99008. enantiome
  99009. intramolecular
  99010. photocycloaddition
  99011. methoxyphenyl
  99012. intramolecular
  99013. photocycloaddition
  99014. double
  99015. intramolecular
  99016. reactions
  99017. chain
  99018. molecules
  99019. intramolecular
  99020. reactions
  99021. diazocarbonyl
  99022. compounds
  99023. intramolecular
  99024. reactions
  99025. n-acyliminium
  99026. intermediates
  99027. intramolecular
  99028. reactivity
  99029. arylcarbenes
  99030. derivatives
  99031. intramolecular
  99032. reductive
  99033. coupling
  99034. carbonyl-tethered
  99035. oxime
  99036. intramolecular
  99037. schmidt
  99038. reactions
  99039. alkyl
  99040. azides
  99041. ketone
  99042. intramolecular
  99043. stoichiometric
  99044. catalytic
  99045. intramolecular
  99046. strategies
  99047. stereoelectronic
  99048. effects
  99049. glyco
  99050. intramolecular
  99051. sulfenylation
  99052. using
  99053. sulfoxides
  99054. preparation
  99055. intramolecularly
  99056. intramoleular
  99057. intrinsic
  99058. introduc
  99059. introduce
  99060. introducing
  99061. introduct
  99062. introduction}
  99063. introduction
  99064. introduction
  99065. acetylene
  99066. moiety
  99067. amide
  99068. carbons
  99069. introduction
  99070. isopropyl
  99071. group
  99072. position
  99073. introduction
  99074. different
  99075. groups
  99076. positions
  99077. introduction
  99078. fluorine
  99079. organic
  99080. molecules
  99081. introduction
  99082. oxygen
  99083. functions
  99084. position
  99085. introduction
  99086. stereochemistry
  99087. conformational
  99088. analysis
  99089. introductory
  99090. inubushi
  99091. inubushi
  99092. harayama
  99093. total
  99094. synthesis
  99095. lycopodium
  99096. alkaloid
  99097. invariants
  99098. invention
  99099. inverse
  99100. inverse
  99101. electron
  99102. demand
  99103. diels
  99104. alder
  99105. reactions
  99106. condensed
  99107. inverse
  99108. electron
  99109. demand
  99110. diels
  99111. alder
  99112. reactions
  99113. heterocycli
  99114. inverse
  99115. electron
  99116. demand
  99117. hetero
  99118. diels
  99119. alder
  99120. reaction
  99121. inversely-fused
  99122. inversion
  99123. invertebrates
  99124. inverted
  99125. investig
  99126. investig
  99127. tions
  99128. synthesis
  99129. alkyl-substituted
  99130. borohyd
  99131. investigated
  99132. investigating
  99133. investigating
  99134. range
  99135. electron
  99136. transfer
  99137. processes
  99138. investigation
  99139. investigation
  99140. molecular
  99141. bonium
  99142. rearrangements
  99143. investigations
  99144. tigations
  99145. furanocembranolide
  99146. diterpene
  99147. constructio
  99148. investigations
  99149. arbuzov
  99150. retro-arbuzov
  99151. reactions
  99152. investigations
  99153. transition
  99154. state
  99155. geometry
  99156. lewis
  99157. invited
  99158. involatile
  99159. involv
  99160. involved
  99161. involvement
  99162. involvi
  99163. involving
  99164. involving
  99165. iodide
  99166. iodinane
  99167. iodination
  99168. iodination
  99169. phenols
  99170. benzyltrimethylammon
  99171. dichlor
  99172. iodine
  99173. iodine
  99174. promoted
  99175. decomposition
  99176. dialkyltriazenes
  99177. iodine
  99178. promoted
  99179. decomposition
  99180. dialkyl
  99181. triazenes
  99182. iodine-cerium
  99183. iodoacetoxylation
  99184. iodoalkanes
  99185. iodoalkyl
  99186. iodoanilides
  99187. iodoaromatic
  99188. iodoaryl
  99189. iodobenzamides
  99190. iodobenzene
  99191. iodobenzene
  99192. diacetate
  99193. related
  99194. hypervalent
  99195. iodine
  99196. reagent
  99197. iodobenzyl
  99198. iodobicyclo
  99199. iodobut
  99200. iodocarbenium
  99201. iodocyclisations
  99202. iodocyclizations
  99203. iodoesters
  99204. iodoetherification
  99205. iodoethyl
  99206. iodolactonizations
  99207. iodomethyl
  99208. iodonium
  99209. erfluoroalkanes
  99210. iodophenol
  99211. iodophenyl
  99212. iodopropyl
  99213. iodosilanes
  99214. iodosuccinimide
  99215. iodosylbenzene
  99216. iodosylbenzene/trime
  99217. iodotrimethylsilane
  99218. iodotrimethylsilane
  99219. versatile
  99220. synthetic
  99221. reagent
  99222. iodotrimethylsilane
  99223. versatile
  99224. synthetic
  99225. reagent
  99226. overview
  99227. ioffe
  99228. ioffe
  99229. leont'eva
  99230. tartakovskii
  99231. chemistry
  99232. alpha
  99233. ioganson
  99234. pairing
  99235. reactivity
  99236. alkali
  99237. metal
  99238. alkoxides
  99239. ion-induced
  99240. ion-oxygen
  99241. ion-pair
  99242. ion-pairing
  99243. ion-pairing
  99244. effects
  99245. carbanion
  99246. reactions
  99247. ion-radical
  99248. ion-radical
  99249. organic
  99250. reactions
  99251. ion-spray
  99252. ion/molecule
  99253. ionic
  99254. iation
  99255. base-promoted
  99256. elimination
  99257. reactions
  99258. ionin
  99259. ionizable
  99260. ionization
  99261. ionization/field
  99262. ionizations
  99263. ionizing
  99264. ionomycin
  99265. ionomycin
  99266. ionophore
  99267. ionophoresy
  99268. ipecac
  99269. iphatic
  99270. ipso-substitutions
  99271. iptycenes
  99272. iptycenes
  99273. cuppedophanes
  99274. cappedophanes
  99275. iqbal
  99276. iqbal
  99277. javed
  99278. bhatia
  99279. beena
  99280. nayyar
  99281. naresh
  99282. transition
  99283. metal
  99284. iranpoor
  99285. iraqi
  99286. ireland
  99287. ireland-claisen
  99288. iridium
  99289. iridium
  99290. compounds
  99291. catalysis
  99292. iridium-catalyzed
  99293. iridoid
  99294. irina
  99295. irinotecan
  99296. irngartinger
  99297. compounds
  99298. organic
  99299. synthesis
  99300. mediated
  99301. synthesis
  99302. heterocyclic
  99303. systems
  99304. iron-carbene
  99305. iron-carbene
  99306. complexes
  99307. iron-containing
  99308. iron-mediated
  99309. iron-mediated
  99310. synthesis
  99311. heterocyclic
  99312. systems
  99313. ironcontaining
  99314. irontricarbonyl
  99315. irontricarbonyl
  99316. complexes
  99317. exocyclic
  99318. polyenes
  99319. irradiate
  99320. irradiated
  99321. irradiation
  99322. irradiations
  99323. irrelationships
  99324. irreversible
  99325. irreversible-process
  99326. irritant
  99327. irritants
  99328. irvin
  99329. irving
  99330. tetramethylethylened
  99331. ligand
  99332. lithium
  99333. n'-tetramethylethyle
  99334. ligand
  99335. lithium
  99336. substitution
  99337. inversion
  99338. configuration
  99339. vinyl
  99340. transition
  99341. state
  99342. indeed
  99343. intermediate
  99344. between
  99345. eactants
  99346. isaacs
  99347. isaacs
  99348. pressure
  99349. methods
  99350. organic
  99351. isabel
  99352. isatin
  99353. isatins
  99354. isatogens
  99355. isatoic
  99356. ishchenko
  99357. ishchenko
  99358. structure
  99359. spectral
  99360. luminescent
  99361. properties
  99362. ishibashi
  99363. ishida
  99364. ishii
  99365. ishii
  99366. nucleophilic
  99367. displacement
  99368. methoxy
  99369. group
  99370. ishikawa
  99371. ishikawa
  99372. kumada
  99373. photochemistry
  99374. organopolysilanes
  99375. ishikura
  99376. ishimaru
  99377. ishizuka
  99378. ishmaeva
  99379. ishmaeva
  99380. polarity
  99381. structure
  99382. unsaturated
  99383. deriv
  99384. isiah
  99385. ismail
  99386. ismailov
  99387. isnin
  99388. isnin
  99389. rahimah
  99390. kaifer
  99391. angel
  99392. approach
  99393. cyclodextrin
  99394. isoalantolactones
  99395. isoalloxazines
  99396. isoannelation
  99397. isoavenaciolide
  99398. isobe
  99399. isobe
  99400. kawaguchi
  99401. organopalladium
  99402. complexes
  99403. containing
  99404. isobe
  99405. minoru
  99406. nishikawa
  99407. toshio
  99408. yamamoto
  99409. noboru
  99410. tskiyama
  99411. takah
  99412. isobel
  99413. isobenzo
  99414. isobenzofuran
  99415. isobenzofuran
  99416. related
  99417. o-quinonoid
  99418. systems
  99419. isobenzofurans
  99420. isobutyl
  99421. isochroman
  99422. isocomene
  99423. isocoumarins
  99424. isocyanate
  99425. isocyanates
  99426. isocyanates
  99427. isocyanato
  99428. isocyani
  99429. isocyanic
  99430. isocyanide
  99431. isocyanides
  99432. isocyanides-recent
  99433. isocyano
  99434. isocyanomethylide
  99435. isoelectronic
  99436. isoepurine
  99437. isoflavonoid
  99438. isoflavonoids
  99439. isoform
  99440. isoimerubrine
  99441. indole
  99442. isoindoles
  99443. isoindolones
  99444. isoinversion
  99445. isoiridomyrmecin
  99446. isolable
  99447. isolated
  99448. isolation
  99449. isolation
  99450. identification
  99451. aromatic
  99452. hydrocarbons
  99453. isolaurepinnacin
  99454. isologues
  99455. isomer
  99456. isomer
  99457. selectivity
  99458. stereocontrolled
  99459. payne
  99460. rearrangeme
  99461. isomerases
  99462. isomeric
  99463. isomerisatio
  99464. isomerisation
  99465. isomerisation
  99466. isomerisation
  99467. diels
  99468. alder
  99469. adducts
  99470. benzoyl
  99471. benzoquin
  99472. isomerisations
  99473. isomerism
  99474. isomerization
  99475. isomerizations
  99476. isomers
  99477. isomunchnone
  99478. isomunchnones
  99479. isonitrile
  99480. isonitriles
  99481. isonitrin
  99482. isono
  99483. isono
  99484. suzuki
  99485. polyoxins
  99486. pyrimidine
  99487. nucleoside
  99488. peptide
  99489. isoparaffins
  99490. isopentenoids
  99491. isoprene
  99492. isoprenoid
  99493. isoprenoids
  99494. isopropoxyalkyl
  99495. isopropyl
  99496. isopropylidene
  99497. isopropyloxazolinyl
  99498. isopyrazoles
  99499. isoquinoline
  99500. isoquinoline
  99501. isoquinoline
  99502. 2-oxides
  99503. isoquinolinequinones
  99504. isoquinolines
  99505. isoquinolines
  99506. benzo
  99507. pyridines
  99508. isoquinolines
  99509. isoquinolinium
  99510. isoquinolinone
  99511. isoquinolones
  99512. isosaccharino
  99513. isosaccharino-lacton
  99514. isosaccharino-lacton
  99515. glucosaccharino-lact
  99516. chirons
  99517. isoschizandrin
  99518. isoseiridine
  99519. isoselective
  99520. isostere
  99521. isosteres
  99522. isosteric
  99523. ydnones
  99524. synthesis
  99525. reactions
  99526. isothiazoles
  99527. isothiazoles
  99528. their
  99529. benzo
  99530. derivatives
  99531. isothiazolo
  99532. isothioc
  99533. isothiochroman
  99534. isothiocyanate
  99535. isothiocyanates
  99536. isothiocyanates
  99537. heterocyclic
  99538. synthesis
  99539. isothiocyanates
  99540. chemistry
  99541. heterocycles
  99542. isothiocyanidate
  99543. isotope
  99544. isotope
  99545. isotopes
  99546. isotopes
  99547. organic
  99548. chemistry
  99549. isotopic
  99550. isotopically
  99551. isotopically
  99552. marked
  99553. carboxylic
  99554. acids
  99555. isotype
  99556. isoureas
  99557. isoxazol
  99558. isoxazole
  99559. isoxazole
  99560. chemistry
  99561. since
  99562. isoxazoles
  99563. isoxazoles
  99564. their
  99565. benzo
  99566. derivatives
  99567. isoxazolidines
  99568. isoxazoline
  99569. isoxazoline-5-spiroc
  99570. isoxazolines
  99571. isoxazolo
  99572. israel
  99573. issam
  99574. issidorides
  99575. issue
  99576. istry
  99577. istvan
  99578. isubstituted
  99579. italiana
  99580. ithaca
  99581. takahashi
  99582. raman
  99583. spectra
  99584. teller
  99585. effec
  99586. yamano
  99587. sumiya
  99588. recent
  99589. progress
  99590. carotenoid
  99591. yoshihiko
  99592. murakami
  99593. masahiro
  99594. metalation
  99595. isocyanides
  99596. yukishige
  99597. gaudino
  99598. paulson
  99599. james
  99600. synthesis
  99601. michiya
  99602. fluorescence
  99603. studies
  99604. excited
  99605. state
  99606. proto
  99607. itokawa
  99608. itokawa
  99609. hideji
  99610. takeya
  99611. koichi
  99612. antitumor
  99613. substances
  99614. highe
  99615. itronates
  99616. itsuno
  99617. iupac
  99618. ivanov
  99619. ivanova
  99620. ivashchenko
  99621. ivermectin
  99622. ivermectin
  99623. seasons
  99624. ivity
  99625. iwamura
  99626. iwamura
  99627. iwamura
  99628. hiizu
  99629. noboru
  99630. studies
  99631. organic
  99632. oligo
  99633. iwaoka
  99634. iwasawa
  99635. iwata
  99636. iwema
  99637. iykkiam
  99638. iyzed
  99639. izatt
  99640. izatt
  99641. christensen
  99642. progress
  99643. macrocyclic
  99644. chemistry
  99645. izatt
  99646. bradshaw
  99647. jerald
  99648. pawlak
  99649. krystyna
  99650. bruening
  99651. izatt
  99652. pawlak
  99653. krystyna
  99654. bradshaw
  99655. jerald
  99656. bruening
  99657. izquierdo
  99658. izquierdo
  99659. medina
  99660. jorge
  99661. naturally
  99662. occurring
  99663. benzodia
  99664. izumi
  99665. izumi
  99666. chibata
  99667. production
  99668. utilization
  99669. amino
  99670. izumi
  99671. iwasawa
  99672. breathing
  99673. ruthenium
  99674. rhodium
  99675. cluster
  99676. izumi
  99677. yusuke
  99678. urabe
  99679. kazuo
  99680. onaka
  99681. makoto
  99682. zeolite
  99683. heter
  99684. izumiya
  99685. izutsu
  99686. izutsu
  99687. kosuke
  99688. dissociation
  99689. constants
  99690. dipolar
  99691. dumesic
  99692. topsoe
  99693. mossbauer
  99694. spectroscopy
  99695. applications
  99696. elvidge
  99697. barot
  99698. imidines
  99699. diamidides
  99700. triaza
  99701. zoltewicz
  99702. fortschritte
  99703. forschung
  99704. apsimon
  99705. holmes
  99706. application
  99707. heterocycles
  99708. harborne
  99709. chemosystematics
  99710. coevolution
  99711. hendrickson
  99712. approaching
  99713. hendrickson
  99714. sternbach
  99715. trifluoromethylsu
  99716. hendrickson
  99717. fortachritte
  99718. forschung
  99719. jones
  99720. tetrahedron
  99721. enzymes
  99722. organic
  99723. synthe
  99724. bauer
  99725. herges
  99726. fountain
  99727. chimia
  99728. powers
  99729. haloketone
  99730. inhibitors
  99731. proteolytic
  99732. enzymes
  99733. sarma
  99734. sharma
  99735. heterocycles
  99736. synthesis
  99737. chenet
  99738. vessiere
  99739. proced
  99740. cornelisse
  99741. havinga
  99742. photosubstituti
  99743. cornelisse
  99744. havinga
  99745. photosubstit
  99746. coyle
  99747. photochemistry
  99748. organic
  99749. sulfu
  99750. coyle
  99751. tetrahedron
  99752. photochemistry
  99753. martin
  99754. darias
  99755. algal
  99756. sesquiterpenoids
  99757. marine
  99758. natura
  99759. martin
  99760. palazon
  99761. perez
  99762. ravelo
  99763. wuest
  99764. tetrahedron
  99765. symposium
  99766. print
  99767. d'angelo
  99768. tetrahedron
  99769. ketone
  99770. enolates
  99771. regiospe
  99772. multistep
  99773. conformational
  99774. interconversion
  99775. mechanisms
  99776. baldwin
  99777. thermally
  99778. forbidden
  99779. reactions
  99780. pericyclic
  99781. reactio
  99782. dubois
  99783. strain
  99784. energy
  99785. modeling
  99786. simple
  99787. crowded
  99788. guiilet
  99789. energy
  99790. transfer
  99791. molecular
  99792. mobility
  99793. polyme
  99794. mcmurry
  99795. ester
  99796. cleavage
  99797. dealkylation
  99798. mills
  99799. maryanoff
  99800. evans
  99801. molecular
  99802. rearrangements
  99803. polynuelear
  99804. transition
  99805. harrod
  99806. chalk
  99807. hydrosilation
  99808. catalyzed
  99809. group
  99810. liebman
  99811. greenberg
  99812. survey
  99813. regitz
  99814. synthesis
  99815. electrophilic
  99816. diazoal
  99817. heterocycl
  99818. reduction
  99819. jones
  99820. sequential
  99821. polypeptide
  99822. synthesis
  99823. chemistry
  99824. perlstein
  99825. organic
  99826. metals
  99827. intermolecular
  99828. migration
  99829. halpern
  99830. angew
  99831. oxidation
  99832. halpern
  99833. catalysis
  99834. symmetry
  99835. restricted
  99836. reactions
  99837. halpern
  99838. lecture
  99839. radical
  99840. principle
  99841. least
  99842. nuclear
  99843. motion
  99844. advan
  99845. hinton
  99846. methodology
  99847. mechanistic
  99848. crowley
  99849. rapoport
  99850. accounts
  99851. cadogan
  99852. hickson
  99853. mcnab
  99854. tetrahedron
  99855. eisch
  99856. rearrangement
  99857. unsaturated
  99858. organoboron
  99859. organ
  99860. gajewski
  99861. transition
  99862. mccullough
  99863. photoadditions
  99864. aromat
  99865. renard
  99866. bolker
  99867. chemistry
  99868. jurczak
  99869. pikul
  99870. bauer
  99871. tetrahedron
  99872. clarke
  99873. selectivity
  99874. catalysis
  99875. rasmussen
  99876. hassner
  99877. recent
  99878. rasmussen
  99879. silylated
  99880. enolates
  99881. versatile
  99882. intermediates
  99883. stille
  99884. james
  99885. transition
  99886. metal
  99887. catalyzed
  99888. carbonyl
  99889. stille
  99890. angew
  99891. palladium
  99892. whitesell
  99893. perspectives
  99894. knabe
  99895. heterocycl
  99896. dihydroisoquinoli
  99897. charlton
  99898. alauddin
  99899. tetrahedron
  99900. 432873
  99901. orthoq
  99902. jensen
  99903. heats
  99904. hydrogenation
  99905. brief
  99906. summary
  99907. morris
  99908. 0rganic
  99909. liebscher
  99910. hartmann
  99911. heterocycles
  99912. diary
  99913. lugtenburg
  99914. synthesis
  99915. barker
  99916. thienopyridines
  99917. advances
  99918. hetero
  99919. conia
  99920. perchec
  99921. synthesis
  99922. thermal
  99923. conia
  99924. leperchec
  99925. synthesis
  99926. thermal
  99927. cycli
  99928. science
  99929. supramolecular
  99930. chemistry
  99931. recep
  99932. patterson
  99933. synthesis
  99934. recent
  99935. synthetic
  99936. methods
  99937. thomas
  99938. morsi
  99939. desvergne
  99940. topochemi
  99941. secondary
  99942. metabolism
  99943. oxford
  99944. university
  99945. press
  99946. tetrahedron
  99947. synthetic
  99948. utility
  99949. meinwald
  99950. approach
  99951. synthesis
  99952. pederin
  99953. mlcoch
  99954. steckhan
  99955. tetrahedron
  99956. electr
  99957. shoolery
  99958. quantitative
  99959. applications
  99960. organometal
  99961. annual
  99962. surveys
  99963. transition
  99964. metals
  99965. organometal
  99966. organometallics
  99967. organic
  99968. synth
  99969. liebscher
  99970. hartmann
  99971. heterocycles
  99972. diary@
  99973. organometal
  99974. ferrocene
  99975. annual
  99976. survey
  99977. cove@
  99978. aldrichimica
  99979. lanthanides
  99980. organic@
  99981. chemistry
  99982. aspartic
  99983. tsuji
  99984. tetrahedron
  99985. general
  99986. synthetic
  99987. metho@
  99988. jackson
  99989. james
  99990. platz
  99991. matthew
  99992. laser
  99993. flashphotolysis
  99994. studie@
  99995. jamsen
  99996. groot
  99997. occurrence
  99998. biological
  99999. activi@
  100000. japan
  100001. jauregg@
  100002. jenkins
  100003. jochen
  100004. johnson
  100005. tominaga
  100006. keisuke
  100007. walker
  100008. gilbert
  100009. jarzeba
  100010. jones
  100011. jonker@
  100012. joullie
  100013. julia@
  100014. klabunde
  100015. accounts
  100016. organic
  100017. chemistry
  100018. vollhardt
  100019. synthesis
  100020. wittig
  100021. reactions
  100022. kaden
  100023. thomas
  100024. functionalized
  100025. tetraazamacrocycles
  100026. ligands
  100027. kaji@
  100028. kalsi@
  100029. kamigata
  100030. organometal
  100031. ferrocene
  100032. annual
  100033. survey
  100034. organometal
  100035. lanthanides
  100036. actinides
  100037. organometal
  100038. organic
  100039. reactions
  100040. selecte
  100041. organometal
  100042. rates
  100043. mechanisms
  100044. organometal
  100045. transition
  100046. metals
  100047. organic
  100048. organometal
  100049. diphenylphosphino
  100050. methan
  100051. organometal
  100052. stereospecific
  100053. synthesis
  100054. collman
  100055. disodium
  100056. tetracarbonylfe
  100057. kutney
  100058. dihydropyridines
  100059. biosynthesis
  100060. synthesis
  100061. kutney
  100062. studies
  100063. indole
  100064. alkaloid
  100065. synthesis
  100066. general
  100067. kutney
  100068. synthesis
  100069. indole
  100070. alkaloids
  100071. total
  100072. synth
  100073. oliver
  100074. rearrangements
  100075. organoaluminum
  100076. compounds
  100077. paolini
  100078. systems
  100079. bridgehead
  100080. nitrogen
  100081. bouchere
  100082. cousse
  100083. mouzin
  100084. tetrahedron
  100085. meter
  100086. liquid
  100087. crystals
  100088. groups
  100089. chemistry
  100090. aldrichimica
  100091. lanthanides
  100092. organic
  100093. rokach
  100094. adams
  100095. synthesis
  100096. bindra
  100097. bindra
  100098. prostaglandin
  100099. synthesis
  100100. academic
  100101. davies
  100102. occurrence
  100103. biosynthesis
  100104. amino
  100105. acids
  100106. pizey
  100107. synthetic
  100108. reagents
  100109. diborane
  100110. dichloro
  100111. schwartz
  100112. labinger
  100113. angew
  100114. schwartz
  100115. labinger
  100116. angew
  100117. simonet
  100118. guillanton
  100119. simonet
  100120. guillanton
  100121. streith
  100122. photochemistry
  100123. heterocyclic
  100124. synthesis
  100125. streith
  100126. photochemistry
  100127. aromatic
  100128. ylides
  100129. rearrangem
  100130. generation
  100131. reactive
  100132. species
  100133. recent
  100134. advances
  100135. organic
  100136. recent
  100137. progress
  100138. polyol
  100139. synthesis
  100140. crown
  100141. ether
  100142. chemistry
  100143. aspartic
  100144. design
  100145. synthesis
  100146. metabol
  100147. ester
  100148. peptide
  100149. synthesis
  100150. microbial
  100151. carbonyl
  100152. reductases
  100153. development
  100154. highly
  100155. selective
  100156. living
  100157. polymerization
  100158. substi
  100159. stereochemical
  100160. control
  100161. micro
  100162. steroids
  100163. reactions
  100164. partial
  100165. synthesis
  100166. enkephalin
  100167. analogs
  100168. versatile
  100169. chiral
  100170. synthons
  100171. groves
  100172. kruper
  100173. metallop
  100174. gupton
  100175. aldrichimica
  100176. useful
  100177. syntheti
  100178. tsuji
  100179. decarbonylation
  100180. reactions
  100181. using
  100182. transition
  100183. metal
  100184. tsuji
  100185. organomet
  100186. years
  100187. organi
  100188. tsuji
  100189. lecture
  100190. synthetic
  100191. tsuji
  100192. tetrahedron
  100193. general
  100194. synthetic
  100195. metho
  100196. greenhill
  100197. enaminones
  100198. chemical
  100199. society
  100200. reviews
  100201. apsimon
  100202. collier
  100203. tetrahedron
  100204. recent
  100205. cooper
  100206. computer
  100207. fourier
  100208. transform
  100209. faller
  100210. fluxional
  100211. nonrigid
  100212. behavior
  100213. transition
  100214. scheeren
  100215. synthetic
  100216. mechani
  100217. weill
  100218. raynal
  100219. synthesis
  100220. formation
  100221. carbon
  100222. carbon
  100223. wolters
  100224. organometall
  100225. wotter
  100226. organomet
  100227. annual
  100228. corey
  100229. organometall
  100230. silafunctional
  100231. jache
  100232. jackman
  100233. jackman
  100234. lloyd
  100235. bortiatynski
  100236. jacqueline
  100237. structures
  100238. lithiu
  100239. jackmann
  100240. jackson
  100241. jackson
  100242. sargeson
  100243. rearrangement
  100244. coordination
  100245. compl
  100246. jackson
  100247. arthur
  100248. angoh
  100249. small
  100250. molecule
  100251. potential
  100252. oxalyl
  100253. jackson
  100254. james
  100255. platz
  100256. matthew
  100257. laser
  100258. flashphotolysis
  100259. studie
  100260. jacob
  100261. jacobi
  100262. jacobi
  100263. peter
  100264. heteriannulation
  100265. total
  100266. synthesis
  100267. furan
  100268. jacobs
  100269. jacobs
  100270. havinga
  100271. photochemistry
  100272. vitamin
  100273. jacobsen
  100274. jacobsen's
  100275. jacox
  100276. jacox
  100277. stabilization
  100278. spectra
  100279. radicals
  100280. jacqueline
  100281. jacques
  100282. jacques
  100283. collet
  100284. wilen
  100285. enantiomers
  100286. racemates
  100287. resol
  100288. jadab
  100289. jadhav
  100290. jaeger
  100291. jaeger
  100292. koehler
  100293. pseudochalcogens
  100294. sulfur
  100295. reports
  100296. jaenicke
  100297. jager
  100298. jagtap
  100299. jaimala
  100300. jaime
  100301. thermodynamics
  100302. binary
  100303. mixtures
  100304. jakob
  100305. jakubke
  100306. james
  100307. james
  100308. hydrogenation
  100309. reactions
  100310. catalyzed
  100311. transition
  100312. jamieson
  100313. jamsen
  100314. jamsen
  100315. groot
  100316. occurrence
  100317. biological
  100318. activi
  100319. jamshed
  100320. janes
  100321. janet
  100322. janiak
  100323. janiak
  100324. christoph
  100325. schumann
  100326. herbert
  100327. bulky
  100328. supracyclopentadi
  100329. janice
  100330. janina
  100331. janine
  100332. janoschek
  100333. janoschek
  100334. rudolf
  100335. structures
  100336. structures
  100337. structures
  100338. janousek
  100339. janovsky
  100340. jansen
  100341. jansen
  100342. groot
  100343. occurrence
  100344. biological
  100345. activi
  100346. jansen
  100347. groot
  100348. synthesis
  100349. drimane
  100350. sesquiterpe
  100351. jansen
  100352. veldhuizen
  100353. schwegler
  100354. bekkum
  100355. janusz
  100356. janzen
  100357. jaouen
  100358. jaouen
  100359. arene
  100360. complexes
  100361. organic
  100362. synthesis
  100363. transition
  100364. japan
  100365. japan
  100366. japanese
  100367. jaqueline
  100368. jaramillo
  100369. jaramillo
  100370. carlos
  100371. knapp
  100372. spencer
  100373. synthesis
  100374. glycoside
  100375. jarman
  100376. jarman
  100377. perfluoroarenes
  100378. novel
  100379. selective
  100380. protecting
  100381. jaromir
  100382. jaroslav
  100383. jarvis
  100384. jarzeba
  100385. jason
  100386. jasperse
  100387. jasperse
  100388. craig
  100389. curran
  100390. dennis
  100391. fevig
  100392. thomas
  100393. radical
  100394. jasperse
  100395. craig
  100396. curran
  100397. dennis
  100398. fevig
  100399. thomas
  100400. radical
  100401. reacti
  100402. jatrophone
  100403. jaundice
  100404. jauregg
  100405. jautelat
  100406. javed
  100407. javier
  100408. jaworek
  100409. jayaramsn
  100410. jeanette
  100411. jedlinski
  100412. jedlinski
  100413. alkali
  100414. metal
  100415. supramolecular
  100416. complexes
  100417. their
  100418. jeffery
  100419. jefford
  100420. jefford
  100421. cadby
  100422. molecular
  100423. mechanisms
  100424. enzyme
  100425. catalyz
  100426. jefford
  100427. concise
  100428. enantiospecific
  100429. syntheses
  100430. jefford
  100431. dioxygenases
  100432. unified
  100433. mechanistic
  100434. jefford
  100435. charles
  100436. photo
  100437. oxygenation
  100438. olefins
  100439. jeffrey
  100440. jeffs
  100441. jeffs
  100442. sceletium
  100443. alkaloids
  100444. 198119
  100445. alkaloids
  100446. jeganathan
  100447. jeker
  100448. jenck
  100449. jencks
  100450. jencks
  100451. enforced
  100452. mechanisms
  100453. general
  100454. catalyze
  100455. jenkins
  100456. jenkins
  100457. jenkins
  100458. organometallic
  100459. reagents
  100460. synthesis
  100461. oxford
  100462. jenks
  100463. jennifer
  100464. jensen
  100465. jerald
  100466. jeremiah
  100467. jeremy
  100468. jermiah
  100469. jerome
  100470. jerry
  100471. jersey
  100472. jerusalem
  100473. jerzy
  100474. jeschke
  100475. jeyaraman
  100476. jeyaraman
  100477. avila
  100478. chemistry
  100479. azabicyclo
  100480. 3.3.1
  100481. nonanes
  100482. jiang
  100483. jiang
  100484. concepts
  100485. studying
  100486. understanding
  100487. jianjun
  100488. jianxin
  100489. jiarong
  100490. jikeli
  100491. jimenez
  100492. jinfeng
  100493. joachim
  100494. joaov
  100495. joc1991
  100496. jochen
  100497. jochen
  100498. jochum
  100499. jochum
  100500. gasteigern
  100501. principle
  100502. minimum
  100503. chemica
  100504. taxol
  100505. taxotere
  100506. tumour
  100507. joerg
  100508. joergen
  100509. joglar
  100510. johan
  100511. johann
  100512. johannes
  100513. johansen
  100514. johnson
  100515. johnson
  100516. tominaga
  100517. keisuke
  100518. walker
  100519. gilbert
  100520. jarzeba
  100521. johnson
  100522. tominaga
  100523. keisuke
  100524. walker
  100525. gilbert
  100526. jarzeba
  100527. johnson
  100528. reactivity
  100529. selectivity
  100530. principle
  100531. johnson
  100532. adams
  100533. joseph
  100534. scott
  100535. randall
  100536. johnson
  100537. reactions
  100538. electrophiles
  100539. sigma
  100540. bonded
  100541. johnson
  100542. oxygenations
  100543. microorganisms
  100544. oxidation
  100545. johnson
  100546. robert
  100547. bethune
  100548. donald
  100549. yannoni
  100550. costantino
  100551. fulle
  100552. johnston
  100553. johnston
  100554. photochemistry
  100555. radicals
  100556. biradicals
  100557. johnstone
  100558. jolley
  100559. jolly
  100560. jolly
  100561. mynott
  100562. application
  100563. spectroscopy
  100564. jonas
  100565. jonas
  100566. alkali
  100567. metal
  100568. transition
  100569. metal
  100570. complexes
  100571. jonathan
  100572. jones
  100573. jones
  100574. jones
  100575. physical
  100576. chemical
  100577. properties
  100578. quinoline
  100579. quinol
  100580. jones
  100581. synthesis
  100582. quinoline
  100583. system
  100584. quinoline
  100585. jones
  100586. guilford
  100587. farahat
  100588. mohammad
  100589. photoinduced
  100590. electron
  100591. jones
  100592. rasmusson
  100593. recent
  100594. advances
  100595. biology
  100596. jones
  100597. synthetic
  100598. applications
  100599. paterno
  100600. buchi
  100601. react
  100602. jones
  100603. bryan
  100604. probing
  100605. specificity
  100606. synthetically
  100607. usefu
  100608. jones
  100609. formation
  100610. peptide
  100611. bonds
  100612. general
  100613. survey
  100614. jones
  100615. amino
  100616. peptide
  100617. synthesis
  100618. oxford
  100619. chemistry
  100620. jones
  100621. chemical
  100622. synthesis
  100623. peptides
  100624. clarendon
  100625. jones
  100626. maitland
  100627. carbenes
  100628. carboranes
  100629. advances
  100630. carben
  100631. jones
  100632. desio
  100633. familiar
  100634. reactions
  100635. organocad
  100636. jones
  100637. pyrroles
  100638. synthesis
  100639. reactivity
  100640. jones
  100641. rearrangements
  100642. carbenes
  100643. nitrenes
  100644. rearrangem
  100645. jonker
  100646. jonsall
  100647. jordan
  100648. jordan
  100649. kenneth
  100650. paddon
  100651. michael
  100652. analysis
  100653. intera
  100654. jordan
  100655. richard
  100656. chemistry
  100657. cationic
  100658. dicyclo
  100659. pentadienyl
  100660. jordan
  100661. robert
  100662. reaction
  100663. mechanisms
  100664. inorganic
  100665. organom
  100666. jorge
  100667. jorgensen
  100668. jorgensen
  100669. hansen
  100670. thomas
  100671. kruse
  100672. becher
  100673. tetrathiafulva
  100674. jorgensen
  100675. william
  100676. computational
  100677. insights
  100678. intermolecular
  100679. jorgenson
  100680. hellmut
  100681. werner
  100682. fischer
  100683. walter
  100684. wimmer
  100685. josef
  100686. joseph
  100687. josephine
  100688. josette
  100689. joshi
  100690. joshi
  100691. recent
  100692. chemistry
  100693. indian
  100694. piper
  100695. species
  100696. joshi
  100697. krishna
  100698. renuka
  100699. dandia
  100700. anshu
  100701. sharma
  100702. kanti
  100703. fluori
  100704. joshua
  100705. joule
  100706. joullie
  100707. joullie
  100708. joullie
  100709. madeleine
  100710. thompson
  100711. tracy
  100712. ninhydrin
  100713. ninhydrin
  100714. journal
  100715. jovanovic
  100716. joyce
  100717. jozef
  100718. juaristi
  100719. juaristi
  100720. attractive
  100721. repulsive
  100722. gauche
  100723. effects
  100724. juaristi
  100725. eusebio
  100726. cuevas
  100727. gabriel
  100728. recent
  100729. studies
  100730. anomer
  100731. juaristi
  100732. eusebio
  100733. introduction
  100734. stereochemistry
  100735. conform
  100736. juaristi
  100737. eusebio
  100738. quintana
  100739. delia
  100740. escalante
  100741. jaime
  100742. enantioselec
  100743. juaristie
  100744. jubian
  100745. judah
  100746. juerg
  100747. juergen
  100748. jueschkke
  100749. juiian
  100750. jujhar
  100751. jujii
  100752. julandine
  100753. julia
  100754. julia-lythgoe
  100755. julian
  100756. julio
  100757. julius
  100758. jumpmg
  100759. jun'ichi
  100760. juneja
  100761. guenther
  100762. sickinger
  100763. annette
  100764. multiple
  100765. peptide
  100766. michael
  100767. substituent
  100768. solvent
  100769. effects
  100770. intramolec
  100771. junge
  100772. jungheim
  100773. jungheim
  100774. shepherd
  100775. design
  100776. antitumor
  100777. prodrugs
  100778. subst
  100779. junjappa
  100780. junji
  100781. junzo
  100782. jurczak
  100783. jurgen
  100784. juris
  100785. justification
  100786. jutand
  100787. aromatic
  100788. heteroaromatic
  100789. compounds
  100790. electrocyc
  100791. jutzi
  100792. juvenile
  100793. sievers
  100794. praetical
  100795. guide
  100796. lanthanide
  100797. shift
  100798. korinek
  100799. electro
  100800. organic
  100801. oxidation
  100802. becker
  100803. formation
  100804. unsaturated
  100805. groups
  100806. vil'davskaya
  100807. petrov
  100808. bishop
  100809. transition
  100810. metal
  100811. catalyz
  100812. joshi
  100813. chand
  100814. heterocycles
  100815. indole
  100816. nicolaou
  100817. petasis
  100818. claremon
  100819. tetrahedron
  100820. nicolaou
  100821. synthesis
  100822. macrolides
  100823. tetrahedron
  100824. lewis
  100825. mulquiney
  100826. formation
  100827. stenhouse
  100828. golankiewicz
  100829. synthesis
  100830. physical
  100831. photochemical
  100832. igarashi
  100833. koenigs
  100834. knorr
  100835. reaction
  100836. advances
  100837. inoue
  100838. matsuura
  100839. saito
  100840. tetrahedron
  100841. klabunde
  100842. accounts
  100843. organic
  100844. chemistry
  100845. jonas
  100846. angew
  100847. reactive
  100848. organome
  100849. krohn
  100850. angew
  100851. total
  100852. synthesis
  100853. joullie
  100854. heterocycles
  100855. rinehart
  100856. shield
  100857. chemistry
  100858. ansamycin
  100859. antib
  100860. rinehart
  100861. mutasynthesis
  100862. antibiotics
  100863. synthesis
  100864. synthetic
  100865. applications
  100866. milan
  100867. peracetic
  100868. organic
  100869. minachev
  100870. khodakov
  100871. nakhshunov
  100872. maruoka
  100873. yamamoto
  100874. angew
  100875. maruoka
  100876. yamamoto
  100877. angew
  100878. matsumoto
  100879. uchida
  100880. synthesis
  100881. organic
  100882. matsumoto
  100883. synthesis
  100884. organic
  100885. synthesis
  100886. applications
  100887. frontier
  100888. molecular
  100889. orbital
  100890. theory
  100891. nakanishi
  100892. photochemical
  100893. studies
  100894. visual
  100895. pigments
  100896. vollhardt
  100897. synthesis
  100898. wittig
  100899. reactions
  100900. vollhardt
  100901. transition
  100902. metal
  100903. catalyzed
  100904. acetylene
  100905. cycliza
  100906. schlogl
  100907. hofer
  100908. twelfth
  100909. smith
  100910. advances
  100911. organoboron
  100912. chemistry
  100913. smith
  100914. preparation
  100915. organoboranes
  100916. potts
  100917. heteropentalenes
  100918. special
  100919. topics
  100920. heterocycli
  100921. radha
  100922. kishan
  100923. desiraju
  100924. wiesner
  100925. tetrahedron
  100926. highlights
  100927. k252a
  100928. kabachnik
  100929. kabachnik
  100930. mastryukova
  100931. fedin
  100932. vaisberg
  100933. morozov
  100934. kabachnik
  100935. progress
  100936. theory
  100937. acids
  100938. bases
  100939. kabalka
  100940. kabalka
  100941. radionuclide
  100942. incorporation
  100943. organoboranes
  100944. kabbe
  100945. yoshio
  100946. wataru
  100947. small
  100948. organo
  100949. silicon
  100950. germanium
  100951. kabouche
  100952. kadaba
  100953. kaden
  100954. kaden
  100955. thomas
  100956. functionalized
  100957. tetraazamacrocycles
  100958. ligands
  100959. kadentsev
  100960. kadish
  100961. kadryov
  100962. kaesz
  100963. kagaku
  100964. kagan
  100965. kagan
  100966. fiaud
  100967. approaches
  100968. asymmetric
  100969. synthesis
  100970. kagan
  100971. henri
  100972. riant
  100973. olivier
  100974. catalytic
  100975. asymmetric
  100976. diels
  100977. alder
  100978. kagan
  100979. naturally
  100980. occurring
  100981. trithiophenes
  100982. kagan
  100983. naturally
  100984. occurring
  100985. trithiophenes
  100986. kagan
  100987. jacques
  100988. organicphotochemistr
  100989. principles
  100990. applicatio
  100991. kagen
  100992. michael
  100993. peptide
  100994. secondary
  100995. structure
  100996. mimetics
  100997. recent
  100998. kaifer
  100999. kaifer
  101000. angel
  101001. cyclodextrin
  101002. complexation
  101003. amphiphilic
  101004. compou
  101005. wolfgang
  101006. thermal
  101007. light
  101008. induced
  101009. electron
  101010. transfer
  101011. kainic
  101012. kainoids
  101013. kaiser
  101014. kaishi
  101015. kaisin
  101016. kaitmazova
  101017. kajfei
  101018. kajimoto
  101019. kakuchi
  101020. kalabin
  101021. kalchenko
  101022. kalck
  101023. kalck
  101024. philippe
  101025. peres
  101026. yolande
  101027. jenck
  101028. hydroformylation
  101029. kalinin
  101030. kalinin
  101031. carbon
  101032. carbon
  101033. formation
  101034. heterocycles
  101035. kalinin
  101036. functionalization
  101037. heterocycles
  101038. kalinkin
  101039. kalinkin
  101040. kolomnikova
  101041. parnes
  101042. kursanov
  101043. catalyt
  101044. kalista
  101045. kaliya
  101046. kalman
  101047. kalmanol
  101048. stereochemistry
  101049. conformation
  101050. mechanism
  101051. wiley
  101052. kamal
  101053. kambouns
  101054. kamerling
  101055. kamerling
  101056. structural
  101057. studies
  101058. glycoprotein
  101059. glycans
  101060. kamernetskii
  101061. kamernitskii
  101062. kamernitzky
  101063. kameswara
  101064. kametani
  101065. kametani
  101066. ihara
  101067. chemical
  101068. biochemical
  101069. aspects
  101070. isoqu
  101071. kametani
  101072. nemoto
  101073. recent
  101074. advances
  101075. total
  101076. synthesis
  101077. kametani
  101078. takahashi
  101079. synthesis
  101080. pyrrolo
  101081. indoles
  101082. kamigata
  101083. kamigata
  101084. kamimura
  101085. kaminski
  101086. kaminskii
  101087. kaminsky
  101088. kamiya
  101089. kamlet
  101090. kamlet
  101091. mortimer
  101092. linear
  101093. solvation
  101094. energy
  101095. relationships
  101096. kammer
  101097. kampars
  101098. kampel
  101099. kamphuis
  101100. kamyar
  101101. kanamori
  101102. kanaoka
  101103. kanaoka
  101104. photoreactions
  101105. cyclic
  101106. imides
  101107. examples
  101108. synthe
  101109. vinayak
  101110. willem
  101111. bickelhaupt
  101112. friedrich
  101113. synthe
  101114. kaneko
  101115. kanemasa
  101116. kanematsu
  101117. kanematsu
  101118. molecular
  101119. design
  101120. syntheses
  101121. biologically
  101122. kanishchev
  101123. kankan
  101124. kanner
  101125. kant}
  101126. kanti
  101127. kantlehner
  101128. kantor
  101129. kaori
  101130. kaoru
  101131. kapil
  101132. kapil
  101133. brown
  101134. monoterpene
  101135. alkaloid
  101136. glycosides
  101137. kaplan
  101138. kaplan
  101139. radicals
  101140. reactive
  101141. intermediates
  101142. jones
  101143. kaplan
  101144. radicals
  101145. reactive
  101146. intermediates
  101147. jones
  101148. kaplan
  101149. trozzolo
  101150. singlet
  101151. oxygen
  101152. degrad
  101153. kappe
  101154. kappe
  101155. oliver
  101156. years
  101157. biginelli
  101158. dihydropyridine
  101159. kappe
  101160. stadlbauer
  101161. isatoic
  101162. anhydrides
  101163. their
  101164. kaprinidis
  101165. karaev
  101166. karaev
  101167. garaeva
  101168. ethers
  101169. russi
  101170. karakhanov
  101171. karakhanov
  101172. kelarev
  101173. polivin
  101174. synthesis
  101175. karcher
  101176. karcher
  101177. devillers
  101178. garrigues
  101179. jacob
  101180. spectral
  101181. karelson
  101182. karimov
  101183. karin
  101184. karle
  101185. karlyn
  101186. karmanova
  101187. karnernitsky
  101188. karnojitzky
  101189. karola
  101190. preparation
  101191. reactions
  101192. indolin
  101193. karpf
  101194. karpyshev
  101195. karsten
  101196. kartashov
  101197. kartashov
  101198. skorobogatova
  101199. zefirov
  101200. reactions
  101201. karzhavina
  101202. kaplan
  101203. trozzolo
  101204. singlet
  101205. oxygen
  101206. degrad@
  101207. katritzky
  101208. jones
  101209. literature
  101210. heterocyclic
  101211. chemi@
  101212. kauffmann
  101213. principle
  101214. areno
  101215. analogy
  101216. heterocyclopolya@
  101217. kedarcidin@
  101218. ketals@
  101219. ketcham@
  101220. ketones
  101221. ketteman@
  101222. khananashvili@
  101223. kholodov@
  101224. kinetics
  101225. kingston
  101226. molinero
  101227. rimoldi
  101228. taxane
  101229. alkaloids@
  101230. kishi
  101231. yoshito
  101232. preferred
  101233. solution
  101234. conformation
  101235. marine
  101236. natu@
  101237. klemm
  101238. correlation
  101239. chemistries
  101240. thienopyri@
  101241. knochel
  101242. singer
  101243. robert
  101244. preparation
  101245. reactions
  101246. kobrina@
  101247. komarov@
  101248. korinek
  101249. kovacs
  101250. kozikovvski
  101251. thiels
  101252. hanin
  101253. israel
  101254. huperaz@
  101255. kraus
  101256. organic
  101257. substituent
  101258. effects
  101259. probes
  101260. mechan@
  101261. kropp
  101262. photochemistry
  101263. alkenes
  101264. solution
  101265. organic
  101266. phot@
  101267. krylov
  101268. methods
  101269. increasing
  101270. efficiency
  101271. catalysi@
  101272. kasai
  101273. kasai
  101274. larsen
  101275. chemistry
  101276. biochemistry
  101277. gamma
  101278. giuta
  101279. kasha
  101280. kasha
  101281. brabham
  101282. singlet
  101283. oxygen
  101284. electronic
  101285. structure
  101286. kasha
  101287. sytnik
  101288. dellinger
  101289. solvent
  101290. spectroscopy
  101291. kashima
  101292. kashima
  101293. synthetic
  101294. reactions
  101295. using
  101296. isoxazole
  101297. compounds
  101298. kashin
  101299. kashman
  101300. kashrnan
  101301. kasmai
  101302. kasukhin
  101303. katagiri
  101304. katawala
  101305. kathleen
  101306. kathryn
  101307. katkevich
  101308. katagiri
  101309. yamamoto
  101310. recent
  101311. advances
  101312. chemistr
  101313. katoh
  101314. katrin
  101315. katritzky
  101316. katritzky
  101317. conversions
  101318. primary
  101319. amino
  101320. groups
  101321. other
  101322. katritzky
  101323. dennis
  101324. recent
  101325. progress
  101326. cycloaddition
  101327. katritzky
  101328. jones
  101329. literature
  101330. heterocyclic
  101331. chemi
  101332. katritzky
  101333. patel
  101334. riddell
  101335. methyl
  101336. inversion
  101337. barri
  101338. katritzky
  101339. karelson
  101340. malhotra
  101341. nageshwar
  101342. heterocycl
  101343. katritzky
  101344. qiang
  101345. mechanisms
  101346. rates
  101347. elect
  101348. katritzky
  101349. gordeev
  101350. mikhail
  101351. heterocyclic
  101352. rearrangemen
  101353. katritzky
  101354. karelson
  101355. harris
  101356. philip
  101357. prototropic
  101358. katritzky
  101359. karelson
  101360. hitchings
  101361. gregory
  101362. cycloaddi
  101363. katritzky
  101364. karelson
  101365. malhotra
  101366. nageshwar
  101367. heterocycl
  101368. katritzky
  101369. jamshed
  101370. heterocyclic
  101371. oxides
  101372. katritzky
  101373. xiangfu
  101374. qiang
  101375. benzotriazole
  101376. katritzky
  101377. rachwal
  101378. stanislaw
  101379. hitchings
  101380. gregory
  101381. benzo
  101382. katritzky
  101383. summary
  101384. katritzky
  101385. research
  101386. group
  101387. scienti
  101388. katsuki
  101389. katsumi
  101390. katsuyuki
  101391. kauffmann
  101392. kauffmann
  101393. search
  101394. organometallic
  101395. reagents
  101396. kauffmann
  101397. principle
  101398. areno
  101399. analogy
  101400. heterocyclopolya
  101401. kaufmann
  101402. kaupp
  101403. kaupp
  101404. photochemical
  101405. rearrangements
  101406. fragmentations
  101407. kaupp
  101408. photochemical
  101409. rearrangements
  101410. fragmentations
  101411. kaupp
  101412. cycloaddition
  101413. reaction
  101414. total
  101415. synthesis
  101416. kaupp
  101417. michael
  101418. absolute
  101419. asymmetric
  101420. synthesis
  101421. kaupp
  101422. gerhard
  101423. resolution
  101424. racemates
  101425. distillation
  101426. kausch
  101427. kavarnos
  101428. kawada
  101429. kawaguchi
  101430. kawai
  101431. kawanishi
  101432. kawasaki
  101433. kawase
  101434. kawauchi
  101435. kazanskii
  101436. kazanskii
  101437. vladimir
  101438. nature
  101439. adsorbed
  101440. carbenium
  101441. kazuhide
  101442. kazuhiko
  101443. kazuhiro
  101444. kazuko
  101445. kazunobu
  101446. kazuo
  101447. keana
  101448. keana
  101449. newer
  101450. aspects
  101451. synthesis
  101452. chemistry
  101453. kearns
  101454. kearns
  101455. solvent
  101456. solvent
  101457. isotope
  101458. effects
  101459. lifeti
  101460. kedarcidin
  101461. keefer
  101462. keehn
  101463. keeler
  101464. keeler
  101465. james
  101466. knowing
  101467. unknown
  101468. chemistry
  101469. britain
  101470. keene
  101471. keese
  101472. keglevic
  101473. keglevic
  101474. glycosiduronic
  101475. acids
  101476. related
  101477. compounds
  101478. keglevich
  101479. keglevich
  101480. gyorgy
  101481. synthesis
  101482. membered
  101483. phosphorus
  101484. keiichi
  101485. keiji
  101486. keiko
  101487. keiko
  101488. voronkov
  101489. methods
  101490. synthesis
  101491. acrolein
  101492. keinan
  101493. keister
  101494. keisuke
  101495. keith
  101496. keizo
  101497. kekule
  101498. kekulean
  101499. kelarev
  101500. keletskaya
  101501. kelley
  101502. kellogg
  101503. kellogg
  101504. richard
  101505. enzyme
  101506. models
  101507. organometallic
  101508. chemistry
  101509. kelly
  101510. racemization
  101511. peptide
  101512. synthesis
  101513. peptides
  101514. william
  101515. organic
  101516. spectroscopy
  101517. freeman
  101518. kendall
  101519. kenichirou
  101520. kenji
  101521. kennard
  101522. kennard
  101523. hunter
  101524. william
  101525. single
  101526. crystal
  101527. structure
  101528. kennedy
  101529. kennedy
  101530. marechal
  101531. carbocationic
  101532. polymerization
  101533. wiley
  101534. kenneth
  101535. kennewell
  101536. kennewell
  101537. taylor
  101538. sulphoximides
  101539. update
  101540. kenny
  101541. kenrich
  101542. kenso
  101543. kensuke
  101544. kensy
  101545. kensy
  101546. grellmann
  101547. heinz
  101548. mosquera
  101549. gonzalez
  101550. manuel
  101551. kerber
  101552. kereszturi
  101553. baker
  101554. marine
  101555. sterols
  101556. natural
  101557. product
  101558. reports
  101559. kerridge
  101560. kertes
  101561. kessar
  101562. kessar
  101563. novel
  101564. route
  101565. condensed
  101566. polynuclear
  101567. systems
  101568. kessler
  101569. kessler
  101570. horst
  101571. peptoids
  101572. approach
  101573. development
  101574. kestner
  101575. ketal
  101576. ketalization
  101577. ketals
  101578. ketene
  101579. ketene
  101580. acetals
  101581. ketene
  101582. chemistry
  101583. second
  101584. golden
  101585. ketene
  101586. cycloadditions
  101587. ketene
  101588. dithioacetals
  101589. organic
  101590. synthesis
  101591. recent
  101592. development
  101593. ketene
  101594. equivalents
  101595. ketene
  101596. equivalents
  101597. diels
  101598. alder
  101599. reaction
  101600. ketene
  101601. ketene
  101602. rearrangement
  101603. substituent
  101604. effects
  101605. ketenes
  101606. ketenimine
  101607. ketenimine
  101608. salts
  101609. 1-diazo-1-alkenes
  101610. ketenimines
  101611. keteniminium
  101612. ketenyl
  101613. ketenylidene
  101614. ketimine
  101615. ketimines
  101616. borinate
  101617. reduction
  101618. 17-asymmetric
  101619. induction
  101620. ketoaldehydes
  101621. ketoamides
  101622. ketocarbenes
  101623. ketoester
  101624. ketoesters
  101625. ketohydrazones
  101626. ketoiminato
  101627. ketoimines
  101628. ketonandsy
  101629. ketone
  101630. peracid
  101631. epoxidation
  101632. ketone
  101633. enolates
  101634. regiospecific
  101635. preparation
  101636. synthetic
  101637. ketone-oefin
  101638. ketones
  101639. ketones
  101640. ketophosphonic
  101641. ketorolac
  101642. ketosteroids
  101643. ketosulfonium
  101644. ketosulphones
  101645. ketoxime
  101646. ketoxime-based
  101647. ketoximes
  101648. ketteman
  101649. ketyl
  101650. ketyls
  101651. keukeleire
  101652. keulks
  101653. keulks
  101654. krenzke
  101655. notermann
  101656. selective
  101657. oxidation
  101658. kevan
  101659. kevan
  101660. copper
  101661. catalysis
  101662. complete
  101663. partial
  101664. kevin
  101665. aspects
  101666. organic
  101667. radical
  101668. chemistry
  101669. khaikin
  101670. khaimova
  101671. khairullin
  101672. khairutdinov
  101673. khakhel
  101674. khalaf
  101675. khaldna
  101676. khaldna
  101677. methods
  101678. calculating
  101679. bases
  101680. rocha
  101681. pyrroloquinolines
  101682. pyrrolo
  101683. ferreira
  101684. rocha
  101685. pyrroloquinolines
  101686. pyrrolo
  101687. ferreira
  101688. rocha
  101689. pyrroloquinolines
  101690. pyrrolo
  101691. khananashvili
  101692. khanapure
  101693. khand
  101694. khardin
  101695. kharitonov
  101696. kharitonov
  101697. sobolev
  101698. panov
  101699. hydroxylatyion
  101700. aroma
  101701. khaskin
  101702. khaskin
  101703. molodova
  101704. torgasheva
  101705. reactions
  101706. phospho
  101707. khemani
  101708. khenkin
  101709. khidekel
  101710. pregna
  101711. pentaranes
  101712. synthesis
  101713. immunotropic
  101714. activitg
  101715. azole
  101716. prostaglandins
  101717. malignant
  101718. geterotsikl
  101719. soedin
  101720. three
  101721. membered
  101722. helerocy
  101723. geterotsikl
  101724. soedin
  101725. synthesis
  101726. furazans
  101727. soedin
  101728. alantolactones
  101729. isoalantolac
  101730. khlebnikov
  101731. khmel'nitskii
  101732. khmel'nitskii
  101733. terent'ev
  101734. dissociative
  101735. ionization
  101736. khodakov
  101737. khoklov
  101738. kholmanskii
  101739. kholmanskii
  101740. zubkov
  101741. dyamaev
  101742. nature
  101743. kholodov
  101744. khomenko
  101745. khomenko
  101746. sakhnrov
  101747. golovina
  101748. synthesis
  101749. khorlin
  101750. khramtsov
  101751. khripach
  101752. khripsch
  101753. khristov
  101754. khristov
  101755. angelov
  101756. petrov
  101757. alkadienes
  101758. khristov
  101759. angelov
  101760. petrov
  101761. 13alkadienes
  101762. their
  101763. khudyakov
  101764. khudyakov
  101765. kuz'min
  101766. oxidation
  101767. reduction
  101768. reactions
  101769. khusainova
  101770. khusainova
  101771. pudovik
  101772. organophosphorus
  101773. compounds
  101774. kiado
  101775. kiaeezadeh
  101776. kibayashi
  101777. mechanisms
  101778. reactivity
  101779. organic
  101780. oxyacids
  101781. kichoom
  101782. kielbasinski
  101783. kienitz
  101784. kienzle
  101785. kieran
  101786. kieybasinski
  101787. kifunensine
  101788. kiguchi
  101789. kiichi
  101790. kikovskaya
  101791. kikucchi
  101792. kikuchi
  101793. kilburn
  101794. kilburn
  101795. jeremy
  101796. patel
  101797. hitesh
  101798. synthetic
  101799. developments
  101800. kilenyi
  101801. kilian
  101802. kilograms
  101803. byeang
  101804. hyean
  101805. curran
  101806. dennis
  101807. asymmetric
  101808. thermal
  101809. reaction
  101810. kyung
  101811. activation
  101812. supero
  101813. kimpe
  101814. kimura
  101815. kimura
  101816. ionic
  101817. photodissociation
  101818. ground
  101819. state
  101820. electr
  101821. kinase
  101822. kinetic
  101823. kinetic
  101824. investigations
  101825. provide
  101826. additional
  101827. evidence
  101828. kinetic
  101829. resolution
  101830. racemic
  101831. chromenes
  101832. asymmetric
  101833. epoxi
  101834. kinetic
  101835. resolution
  101836. racemic
  101837. olefins
  101838. asymmetric
  101839. dihydro
  101840. kinetic
  101841. thermodynamic
  101842. determinants
  101843. sequence
  101844. select
  101845. kinetically
  101846. kinetically-controll
  101847. kinetics
  101848. kinetics
  101849. kinetics
  101850. mechanism
  101851. catalyzed
  101852. decomposition
  101853. kinetics
  101854. mechanism
  101855. oxidation
  101856. organoelement
  101857. compoun
  101858. kinetics
  101859. mechanism
  101860. oxidation
  101861. organic
  101862. compounds
  101863. kinetics
  101864. spectroscopy
  101865. carbenes
  101866. biradicals
  101867. kinetics
  101868. intramolecular
  101869. alkyl
  101870. radical
  101871. attack
  101872. sulfur
  101873. kinetics
  101874. nucleophilic
  101875. substitution
  101876. reactions
  101877. polyfluor
  101878. monoolefin
  101879. allyl
  101880. diene
  101881. complexes
  101882. organ
  101883. phosphorus
  101884. bridging
  101885. carbonyl
  101886. derivatives
  101887. organophos
  101888. kingdom
  101889. kinghorn
  101890. kingma
  101891. kingsbury
  101892. kingsbury
  101893. conformations
  101894. substituted
  101895. ethanes
  101896. kingston
  101897. kingston
  101898. molinero
  101899. rimoldi
  101900. taxane
  101901. alkaloids
  101902. kinoshita
  101903. kiplin
  101904. kiplinger
  101905. kiplinger
  101906. jaqueline
  101907. richmond
  101908. thomas
  101909. osterberg
  101910. carolyn
  101911. kirby
  101912. kirby
  101913. effective
  101914. molarities
  101915. intramolecular
  101916. reactions
  101917. kirby
  101918. anthony
  101919. crystallographic
  101920. approaches
  101921. transition
  101922. kirby
  101923. anthony
  101924. enzyme
  101925. mimics
  101926. angewandte
  101927. chemie
  101928. internationa
  101929. kirillov
  101930. kirillova
  101931. kirmse
  101932. kirmse
  101933. rearrangements
  101934. carbocations
  101935. stereochemistry
  101936. kirmse
  101937. wolfgang
  101938. carbenes
  101939. advances
  101940. carben
  101941. kirsh
  101942. kirst
  101943. kirtane
  101944. kisch
  101945. kisch
  101946. horst
  101947. holzmeier
  101948. peter
  101949. organometallic
  101950. chemistry
  101951. kiselev
  101952. kisfaludy
  101953. kisfaludy
  101954. proteins
  101955. peptides
  101956. special
  101957. methods
  101958. kishan
  101959. kishi
  101960. kishi
  101961. yoshito
  101962. applications
  101963. nickel
  101964. chromium
  101965. mediated
  101966. kishi
  101967. yoshito
  101968. preferred
  101969. solution
  101970. conformation
  101971. marine
  101972. kishner
  101973. kisielowski
  101974. kisilitsa
  101975. kislenko
  101976. kislenko
  101977. berlin
  101978. kinetics
  101979. mechanism
  101980. oxidat
  101981. kitaev
  101982. kitagawa
  101983. kitahara
  101984. kitahara
  101985. kinoshita
  101986. miyake
  101987. hasegawa
  101988. watanabe
  101989. kitamura
  101990. kitazume
  101991. kiyoshi
  101992. kjaer
  101993. kjell
  101994. klaas
  101995. klabunde
  101996. klabunde
  101997. metal
  101998. atoms
  101999. reactive
  102000. intermediates
  102001. reactive
  102002. klabunovskii
  102003. klabunovskii
  102004. asymmetric
  102005. hydrogenation
  102006. metals
  102007. russian
  102008. klaffke
  102009. klair
  102010. klarner
  102011. klaui
  102012. klauke
  102013. klaus
  102014. klebe
  102015. klebe
  102016. gerhard
  102017. crystal
  102018. together
  102019. other
  102020. kleemann
  102021. klein
  102022. kleinschroth
  102023. klemchuk
  102024. klemens
  102025. klemm
  102026. klemm
  102027. correlation
  102028. chemistries
  102029. thienopyri
  102030. klemperer
  102031. klemperer
  102032. spectroscopy
  102033. structural
  102034. probe
  102035. klempier
  102036. klessinger
  102037. klessinger
  102038. michl
  102039. excited
  102040. states
  102041. photochemistry
  102042. klessinger
  102043. rademacher
  102044. conformational
  102045. analysis
  102046. photoel
  102047. klibanov
  102048. kliger
  102049. klimo
  102050. klingemann
  102051. klinger
  102052. klinkert
  102053. kloetzel
  102054. kloosterman
  102055. kloostermnn
  102056. klopffer
  102057. kluge
  102058. kluger
  102059. klumpp
  102060. klunder
  102061. kluwer
  102062. klyne
  102063. klyne
  102064. buckingham
  102065. atlas
  102066. stereochemistry
  102067. absolute
  102068. confi
  102069. klyuev
  102070. klyuev
  102071. khidekel
  102072. catalytic
  102073. amination
  102074. alcohols
  102075. knabe
  102076. knapp
  102077. knauer
  102078. knauth
  102079. knight
  102080. knight
  102081. synthetic
  102082. approaches
  102083. butenolides
  102084. contemporary
  102085. knirel
  102086. knobler
  102087. knochel
  102088. knochel
  102089. rozema
  102090. michael
  102091. tucker
  102092. charles
  102093. retherford
  102094. knochel
  102095. singer
  102096. robert
  102097. preparation
  102098. reactions
  102099. knoelker
  102100. knoelker
  102101. joachim
  102102. mediated
  102103. synthesis
  102104. heterocycli
  102105. knoevenagel
  102106. knoll
  102107. knops
  102108. knorr
  102109. knorr
  102110. preparative
  102111. chemistry
  102112. cyclobutendione
  102113. knorre
  102114. knorre
  102115. fedorova
  102116. frolova
  102117. oxidative
  102118. degradation
  102119. knothe
  102120. knots
  102121. knotted
  102122. knowles
  102123. knunyants
  102124. knutov
  102125. knutson
  102126. knuynants
  102127. kobayashiz
  102128. kobayashi
  102129. jun'ichi
  102130. ishibashi
  102131. masami
  102132. marine
  102133. alkaloids
  102134. kobayashi
  102135. kitagawa
  102136. bioactive
  102137. substances
  102138. isolated
  102139. kobayashi
  102140. earth
  102141. metal
  102142. trifluoromethanesulf
  102143. water
  102144. kobayashi
  102145. kumadaki
  102146. reactions
  102147. aromatic
  102148. trifluoromethyl
  102149. kobayashi
  102150. kumadaki
  102151. valence
  102152. isomers
  102153. aromatic
  102154. kober
  102155. koblik
  102156. kobrakov
  102157. kobrina
  102158. kobrina
  102159. peculiarities
  102160. radical
  102161. reactions
  102162. polyf
  102163. kobryanskii
  102164. photochemical
  102165. reactivity
  102166. imino
  102167. ethers
  102168. kochany
  102169. kochetkov
  102170. kochetkov
  102171. kudrjashov
  102172. chlenov
  102173. radiation
  102174. chemistry
  102175. kochetkova
  102176. kochetkova
  102177. krynkina
  102178. practical
  102179. applications
  102180. cyclo
  102181. kochi
  102182. kochi
  102183. organic
  102184. mechanisms
  102185. catalysis
  102186. academic
  102187. press
  102188. kochi
  102189. bockman
  102190. michael
  102191. organometallic
  102192. kochi
  102193. electron
  102194. transfer
  102195. thermal
  102196. photochemic
  102197. kochi
  102198. inner
  102199. sphere
  102200. electron
  102201. transfer
  102202. organic
  102203. chemis
  102204. kodansha
  102205. koehler
  102206. koehler
  102207. gottfried
  102208. rechthaler
  102209. solvent
  102210. effects
  102211. excited
  102212. koelle
  102213. koelle
  102214. ulrich
  102215. energetic
  102216. constitutional
  102217. hysteresis
  102218. koenigs
  102219. koenigs-knorr
  102220. koester
  102221. asymmetric
  102222. synthesis
  102223. mediated
  102224. chiral
  102225. ligands
  102226. kogan
  102227. kohei
  102228. kohler
  102229. kohler
  102230. bryan
  102231. octatetraene
  102232. photoisomerization
  102233. kohlpaintner
  102234. kohnke
  102235. kohnke
  102236. franz
  102237. mathias
  102238. stoddart
  102239. fraser
  102240. substrate
  102241. kohra
  102242. koichi
  102243. koichioro
  102244. koike
  102245. koizumi
  102246. kolbah
  102247. kolbanovskii
  102248. kolbe
  102249. kolbe
  102250. reactions
  102251. kolchina
  102252. kolczewski
  102253. koldobskii
  102254. koldobskii
  102255. ostrovskii
  102256. gidaspov
  102257. schmidt
  102258. reaction
  102259. kolesov
  102260. koljo
  102261. kollonitsch
  102262. kollonitsch
  102263. novel
  102264. methods
  102265. selective
  102266. fluorination
  102267. kolodyazhnyi
  102268. kolodyazhnyi
  102269. halogen
  102270. substituted
  102271. phosphorus
  102272. ylids
  102273. kolomiets
  102274. kolomnikova
  102275. kolter
  102276. kolycheva
  102277. komalenkova
  102278. komarov
  102279. komarova
  102280. komatsu
  102281. komatsu
  102282. koichi
  102283. chemistry
  102284. cyclic
  102285. systems
  102286. surrounded
  102287. komeczny
  102288. komeczny
  102289. sosnovsky
  102290. chemistry
  102291. organo
  102292. phosphorus
  102293. compou
  102294. komiyama
  102295. komno
  102296. komoroski
  102297. kompantseva
  102298. kondo
  102299. konieczny
  102300. konieczny
  102301. sosnovsky
  102302. methods
  102303. preparation
  102304. konig
  102305. konig
  102306. magnetic
  102307. properties
  102308. organic
  102309. chemistry
  102310. konishi
  102311. konnecke
  102312. konovalov
  102313. konovalova
  102314. konrad
  102315. konradsson
  102316. koomen
  102317. koomen
  102318. synthesis
  102319. biological
  102320. properties
  102321. selected
  102322. kopecky
  102323. kopecky
  102324. organic
  102325. photochemistry
  102326. visual
  102327. approach
  102328. kopelevich
  102329. kopelevich
  102330. medicinal
  102331. drugs
  102332. based
  102333. gamma
  102334. aminobutyric
  102335. koppel
  102336. koptyug
  102337. korbonits
  102338. korbonits
  102339. horvath
  102340. synthesis
  102341. heterocycles
  102342. aminoam
  102343. korchak
  102344. korchevin
  102345. korhsunova
  102346. korinek
  102347. korinek
  102348. kormer
  102349. kornblum
  102350. korneeva
  102351. korol
  102352. korol
  102353. chromatographic
  102354. analysis
  102355. products
  102356. korolev
  102357. koroleva
  102358. koroniak
  102359. korpela
  102360. korshak
  102361. korth
  102362. korzeniowski
  102363. koser
  102364. koshits
  102365. koskimies
  102366. koskinen
  102367. kosolapoff
  102368. kosower
  102369. gromov
  102370. sagitullin
  102371. pyridine
  102372. nucleophili
  102373. kosta
  102374. koster
  102375. kostikov
  102376. kosugi
  102377. kosuke
  102378. kosyrev
  102379. kotali
  102380. kotali
  102381. antigoni
  102382. harris
  102383. philip
  102384. hydroxyaryl
  102385. ketones
  102386. kotali
  102387. antigoni
  102388. papageorgiou
  102389. vassilios
  102390. chemistry
  102391. kotel'nikov
  102392. koten
  102393. kotha
  102394. kotha
  102395. sambasivarao
  102396. opportunities
  102397. asymmetric
  102398. synthesis
  102399. kotsuki
  102400. kotsuki
  102401. hiyoshizo
  102402. bicyclic
  102403. ketals
  102404. versatile
  102405. intermediates
  102406. koukoua
  102407. koutecky
  102408. kouwenhoven
  102409. kovacic
  102410. kovacs
  102411. kovacs
  102412. kovacs
  102413. racemization
  102414. coupling
  102415. rates
  102416. protected
  102417. kovacs
  102418. lajos
  102419. methods
  102420. synthesis
  102421. alpha
  102422. esters
  102423. koval
  102424. koval
  102425. progress
  102426. chemistry
  102427. perhalomethanesulphe
  102428. koval
  102429. progress
  102430. chemistry
  102431. sulfilimines
  102432. koval
  102433. sulfides
  102434. organic
  102435. synthesis
  102436. applications
  102437. koval
  102438. sulfides
  102439. synthesis
  102440. properties
  102441. russian
  102442. chemical
  102443. koval
  102444. thiols
  102445. synthons
  102446. russian
  102447. chemical
  102448. reviews
  102449. koval
  102450. advances
  102451. chemistry
  102452. sulfimides
  102453. kovalenko
  102454. kovtunenko
  102455. kowarsch
  102456. koyarna
  102457. koz'min
  102458. kozhevnikov
  102459. kozhevnikov
  102460. organic
  102461. synthesis
  102462. heter
  102463. kozhevnikov
  102464. matveev
  102465. oxidative
  102466. coupling
  102467. aromatic
  102468. kozhushko
  102469. koziar
  102470. koziar
  102471. cowan
  102472. photochemical
  102473. heavy
  102474. effects
  102475. 197811
  102476. kozikovvski
  102477. kozikovvski
  102478. thiels
  102479. hanin
  102480. israel
  102481. huperaz
  102482. kozikowski
  102483. kozikowski
  102484. lewin
  102485. blumberg
  102486. palladium
  102487. kozikowski
  102488. synthesis
  102489. substituted
  102490. indoies
  102491. their
  102492. kozina
  102493. kozlowski
  102494. kozyukov
  102495. krach
  102496. kraerner
  102497. kraeutler
  102498. krafft
  102499. kragelob
  102500. krajnik
  102501. krakowiak
  102502. krakowiak
  102503. kryzsztof
  102504. bradshaw
  102505. jerald
  102506. izatt
  102507. improve
  102508. krakowiak
  102509. krzysztof
  102510. bradshaw
  102511. jerald
  102512. haoyun
  102513. izatt
  102514. kramer
  102515. krantz
  102516. krantz
  102517. thoughts
  102518. enzyme
  102519. inhibitors
  102520. quies
  102521. krapcho
  102522. krapcho
  102523. synthesis
  102524. carbocyclic
  102525. spiro
  102526. compounds
  102527. krasil'nikova
  102528. krasil'nikova
  102529. structure
  102530. reactivity
  102531. esters
  102532. krasnokutskaya
  102533. krasovitskii
  102534. kratochvil
  102535. kratochvll
  102536. kratz
  102537. kratzer
  102538. kraus
  102539. kraus
  102540. organic
  102541. substituent
  102542. effects
  102543. probes
  102544. mechan
  102545. kraus
  102546. patchornik
  102547. polymeric
  102548. carriers
  102549. immobilizing
  102550. kravtsov
  102551. krebs
  102552. krechl
  102553. kreevoy
  102554. kreider
  102555. kreissl
  102556. kreitsberga
  102557. kreitsberga
  102558. neiland
  102559. arylated
  102560. cyclopentadienes
  102561. krentsel
  102562. krenzke
  102563. krepski
  102564. kresge
  102565. kresze
  102566. kreutzer
  102567. krief
  102568. krief
  102569. synthetic
  102570. methods
  102571. using
  102572. heterosubstituted
  102573. organome
  102574. krimen
  102575. krimer
  102576. krinsky
  102577. krinsky
  102578. biological
  102579. roles
  102580. singlet
  102581. oxygen
  102582. singlet
  102583. oxyge
  102584. krishna
  102585. krishnamurthy
  102586. kristina
  102587. krivdin
  102588. krivoshei
  102589. kroger
  102590. krogh
  102591. krohn
  102592. krohn
  102593. karsten
  102594. kirst
  102595. herbert
  102596. antibiotics
  102597. krohnke
  102598. kroker
  102599. krone
  102600. krongauz
  102601. krook
  102602. kropp
  102603. kropp
  102604. photochemistry
  102605. alkenes
  102606. solution
  102607. organic
  102608. kroto
  102609. kroto
  102610. allaf
  102611. buckminsterfullerene
  102612. kroto
  102613. allaf
  102614. buckminsterfullerene
  102615. kroto
  102616. taylor
  102617. walton
  102618. structure
  102619. reactivity
  102620. kroto
  102621. walton
  102622. fullerenes
  102623. horizons
  102624. kroto
  102625. harold
  102626. buckminsterfullerene
  102627. celestial
  102628. sphere
  102629. krotovich
  102630. nitrogen
  102631. insertion
  102632. reactions
  102633. bridged
  102634. bicyclic
  102635. oxygen
  102636. insertion
  102637. reactions
  102638. bridged
  102639. bicyclic
  102640. grant
  102641. bayer
  102642. villiger
  102643. oxidation
  102644. ketones
  102645. krstulovic
  102646. kruchten
  102647. kruger
  102648. kruger
  102649. barnett
  102650. brauer
  102651. structure
  102652. bonding
  102653. organ
  102654. kruglaya
  102655. kruglaya
  102656. vyazankin
  102657. organometallic
  102658. derivatives
  102659. krumpe
  102660. kruper
  102661. kruse
  102662. krutikov
  102663. krygowski
  102664. krylov
  102665. krylov
  102666. methods
  102667. increasing
  102668. efficiency
  102669. catalysi
  102670. krylov
  102671. partial
  102672. catalytic
  102673. oxidation
  102674. methane
  102675. krynkina
  102676. krystyna
  102677. kryzsztof
  102678. krzysztof
  102679. kubanek
  102680. kucera
  102681. kucherov
  102682. kuczkowski
  102683. kuczkowski
  102684. ozonolysis
  102685. vinyl
  102686. ethers
  102687. advances
  102688. oxygen
  102689. kuczkowski
  102690. robert
  102691. structure
  102692. mechanism
  102693. formation
  102694. kudaroski
  102695. takako
  102696. nagase
  102697. shigeru
  102698. cations
  102699. strained
  102700. polycyclic
  102701. kudrjashov
  102702. kuehne
  102703. kuehnle
  102704. kueper
  102705. kuhla
  102706. kuhle
  102707. kuhlmann
  102708. kuk'har
  102709. kuk'har
  102710. svistunova
  102711. solodenko
  102712. soloshonok
  102713. kukhar
  102714. kukhar
  102715. soloshonok
  102716. aliphatic
  102717. fluorine
  102718. containing
  102719. kukhar
  102720. yagupol'skii
  102721. gerus
  102722. kolycheva
  102723. fluorin
  102724. kuklin
  102725. kukolja
  102726. kukovinets
  102727. kukushkin
  102728. kukushkin
  102729. deoxygenation
  102730. coordinated
  102731. sulfoxi
  102732. kulinkovich
  102733. kulinkovich
  102734. activated
  102735. cyclopropanes
  102736. synthesis
  102737. kulka
  102738. kulkarni
  102739. kumabe
  102740. kumada
  102741. kumadaki
  102742. kumadaki
  102743. itsumaro
  102744. steric
  102745. effect
  102746. trifluo
  102747. romethyl
  102748. group
  102749. kumagai
  102750. kumar
  102751. kumazaki
  102752. kunau
  102753. kunesch
  102754. kungS
  102755. kuniaki
  102756. kunieda
  102757. kunio
  102758. kunitake
  102759. kunitake
  102760. shinkai
  102761. catalysis
  102762. micelles
  102763. membranes
  102764. kunshenko
  102765. horst
  102766. karola
  102767. carbohydrates
  102768. chiral
  102769. auxiliaries
  102770. kurasawa
  102771. kurashev
  102772. kuroda
  102773. kuroyan
  102774. kuroyan
  102775. synthesis
  102776. spirone
  102777. piperidine4
  102778. hetero
  102779. kurreck
  102780. kurreck
  102781. harry
  102782. triplet
  102783. states
  102784. organic
  102785. chemistry
  102786. angewandte
  102787. kursanov
  102788. kurts
  102789. kurtz
  102790. kurylo
  102791. kurzer
  102792. kustin
  102793. kukushkin
  102794. deoxygenation
  102795. coordinated
  102796. sulfoxi@
  102797. kutateladze@
  102798. kuznetsova
  102799. kaliya
  102800. photochemistry
  102801. coumarins
  102802. volodarsky
  102803. tikhonov
  102804. synthesis
  102805. synthesi@
  102806. tolbert
  102807. photoexcited
  102808. states
  102809. lactal@
  102810. lactam
  102811. lactams
  102812. catalyzed
  102813. closure
  102814. unsaturated
  102815. heinrich
  102816. novel
  102817. carbon
  102818. compounds
  102819. naked
  102820. units
  102821. large
  102822. laser
  102823. flash
  102824. photolysis
  102825. studies
  102826. ylide
  102827. forming
  102828. reactions
  102829. lautens@
  102830. leading
  102831. degenerate
  102832. rearrangements
  102833. triarylvinyl
  102834. cations
  102835. legon
  102836. nature
  102837. ammonium
  102838. methylammonium
  102839. halides
  102840. lemieux
  102841. raymond
  102842. explorations
  102843. sugars
  102844. sweet
  102845. lerman
  102846. skeletal
  102847. rearrangements
  102848. compounds
  102849. levoglucosenone
  102850. properties
  102851. reactions
  102852. kutateladze
  102853. kutchan
  102854. kutchan
  102855. dittrich
  102856. bracher
  102857. enzymology
  102858. kuthan
  102859. kuthan
  102860. sebek
  102861. developments
  102862. chemistry
  102863. kuthan
  102864. josef
  102865. extension
  102866. decker
  102867. oxidation
  102868. heterocycles
  102869. kutney
  102870. kutney
  102871. studies
  102872. plant
  102873. tissue
  102874. cultures
  102875. kutney
  102876. james
  102877. plant
  102878. culture
  102879. combined
  102880. chemistry
  102881. kutney
  102882. james
  102883. plant
  102884. cultures
  102885. synthetic
  102886. chemistry
  102887. kutyrev
  102888. kutyrev
  102889. moskva
  102890. nucleophilic
  102891. reactions
  102892. quinones
  102893. kutyrev
  102894. moskva
  102895. nucleophilic
  102896. reactions
  102897. quinones
  102898. kutyrev
  102899. nucleophilic
  102900. reactions
  102901. quinones
  102902. tetrahedron
  102903. kutzelnigg
  102904. kuwajima
  102905. kuz'min
  102906. kuz'mina
  102907. kuznetsov
  102908. kuznetsov
  102909. diazenium
  102910. salts
  102911. russian
  102912. chemical
  102913. kuznetsova
  102914. kuznetsova
  102915. kaliya
  102916. photochemistry
  102917. coumarins
  102918. kvasnicka
  102919. kwart
  102920. kwock
  102921. kybett
  102922. kyler
  102923. kyoichi
  102924. kyoji
  102925. kyoung
  102926. kyozo
  102927. kyriacos
  102928. kyriacou
  102929. kyriacou
  102930. basics
  102931. electroorganic
  102932. synthesis
  102933. wiley
  102934. inters
  102935. kyung
  102936. paquette
  102937. silyl
  102938. substituted
  102939. cyclopro
  102940. paquette
  102941. synthesis
  102942. preparative
  102943. aspects
  102944. silve
  102945. paquette
  102946. tetrahedron
  102947. renaissance
  102948. slotin
  102949. methods
  102950. phosphorylation
  102951. biological
  102952. molecule
  102953. yanovskaya
  102954. dombrovskii
  102955. yanovskaya
  102956. dombrovskii
  102957. volodarsky
  102958. tikhonov
  102959. synthesis
  102960. synthesi
  102961. baiocchi
  102962. arenes
  102963. freedman
  102964. organometall
  102965. dolby
  102966. glover
  102967. london
  102968. fluoroorganic
  102969. compou
  102970. dolby
  102971. glover
  102972. speciality
  102973. intermediates
  102974. gusel'nikov
  102975. nametkin
  102976. vdorin
  102977. engman
  102978. synthetic
  102979. applications
  102980. field
  102981. disulfides
  102982. polysulfides
  102983. organic
  102984. chemistry
  102985. whitesides
  102986. enzym
  102987. ghosez
  102988. o'donnell
  102989. pericyclic
  102990. reactions
  102991. cumulenes
  102992. hough
  102993. richardson
  102994. recent
  102995. aspects
  102996. chemistry
  102997. mathias
  102998. overberger
  102999. synth
  103000. synthes
  103001. jackmann
  103002. lange
  103003. structure
  103004. reactivity
  103005. alkal
  103006. stock
  103007. classic
  103008. mechanism
  103009. aromatic
  103010. nitration
  103011. tolbert
  103012. photoexcited
  103013. states
  103014. tolbert
  103015. photoexcited
  103016. states
  103017. marko
  103018. organomet
  103019. review
  103020. transition
  103021. minale
  103022. terpenoids
  103023. marine
  103024. sponges
  103025. marine
  103026. natural
  103027. produ
  103028. rasteikiene
  103029. greiciute
  103030. lin'kova
  103031. knunyants
  103032. hegedus
  103033. palladium
  103034. hegedus
  103035. organometal
  103036. transition
  103037. metals
  103038. hegedus
  103039. organometal
  103040. transition
  103041. metals
  103042. hegedus
  103043. organometall
  103044. transition
  103045. kobrina
  103046. radical
  103047. reactions
  103048. aromatic
  103049. polyfluorocompound
  103050. levitt
  103051. widing
  103052. alkyl
  103053. inductive
  103054. effect
  103055. calcula
  103056. szabo
  103057. structural
  103058. features
  103059. bordetella
  103060. pertussis
  103061. l'abbe
  103062. l'abbe
  103063. heterocyclic
  103064. analogues
  103065. methylenecyclopropan
  103066. l-a-amino
  103067. l-amino
  103068. l-proline
  103069. l-sized
  103070. l3-phosphorines
  103071. l5-phosphorines
  103072. l99248
  103073. la-li-66'-disubstitu
  103074. laarhoven
  103075. laatsch
  103076. laatsch
  103077. hartmut
  103078. conocurvone
  103079. prototype
  103080. class
  103081. labar
  103082. labat
  103083. labdane
  103084. labeish
  103085. label
  103086. labeled
  103087. labeling
  103088. labelled
  103089. labels
  103090. labert
  103091. labia
  103092. labile
  103093. labinger
  103094. lablache
  103095. laboratory
  103096. laboureur
  103097. lactacystin
  103098. lactam
  103099. lactam/lactone
  103100. lactamases
  103101. lactams
  103102. catalyzed
  103103. closure
  103104. unsaturated
  103105. lactarane
  103106. lactate
  103107. lactic
  103108. lactim
  103109. lactols
  103110. lactonalkaloide
  103111. lactone
  103112. lactone
  103113. synthesis
  103114. electron
  103115. transfer
  103116. radical
  103117. chemistry
  103118. lactones
  103119. lactones
  103120. lactonic
  103121. ladder
  103122. ladderanes
  103123. ladislav
  103124. ladybug
  103125. laemmle
  103126. lafont
  103127. laforet
  103128. laguna
  103129. lahav
  103130. grignard
  103131. reagents
  103132. chemically
  103133. activated
  103134. magnesiu
  103135. organic
  103136. reductive
  103137. coupling
  103138. titanium
  103139. vanadiu
  103140. conformational
  103141. behavior
  103142. dithiametacy
  103143. thian
  103144. dihydropyrenes
  103145. further
  103146. laibinis
  103147. laidler
  103148. laird
  103149. laird
  103150. energy
  103151. storage
  103152. photochemical
  103153. reactions
  103154. lajos
  103155. lakhontov
  103156. lakhontov
  103157. prokopov
  103158. advances
  103159. chemistry
  103160. lakhvich
  103161. lakhvich
  103162. khripach
  103163. zhabinskii
  103164. synthesis
  103165. brassi
  103166. lakhvich
  103167. pashkovskii
  103168. koroleva
  103169. heteroprostanoids
  103170. lalezari
  103171. lalezari
  103172. shafiee
  103173. yalpani
  103174. selenium
  103175. nitrogen
  103176. heterocycle
  103177. lalonde
  103178. lalonde
  103179. intramolecular
  103180. iminium
  103181. sulfide
  103182. charge
  103183. transf
  103184. lamar
  103185. lamare
  103186. lambda4-trithiapenta
  103187. lambda5-phosphazenes
  103188. lambert
  103189. lambert
  103190. schleyer
  103191. polar
  103192. organometallic
  103193. compound
  103194. lambert
  103195. holcomb
  103196. magyar
  103197. inductive
  103198. enhanc
  103199. lambert
  103200. joseph
  103201. takeuchi
  103202. yoshito
  103203. acyclic
  103204. organonitrogen
  103205. lambert
  103206. joseph
  103207. takeuchi
  103208. yoshito
  103209. cyclic
  103210. organonitrogen
  103211. lambeth
  103212. lammertsma
  103213. lander
  103214. landesberg
  103215. landesberg
  103216. stabilizing
  103217. unstable
  103218. species
  103219. carbonyl
  103220. landini
  103221. landis
  103222. landmarks
  103223. landmarks
  103224. organofluorine
  103225. chemistry
  103226. landmarks
  103227. evolution
  103228. heterogeneous
  103229. catalysts
  103230. landor
  103231. selective
  103232. reductions
  103233. using
  103234. metal
  103235. hydrides
  103236. heinrich
  103237. novel
  103238. carbon
  103239. compounds
  103240. naked
  103241. units
  103242. lange
  103243. langis
  103244. lankacidin
  103245. lanny
  103246. lanosterol
  103247. lanthanide
  103248. lanthanide
  103249. catalyzed
  103250. enantioselective
  103251. diels
  103252. alder
  103253. reacti
  103254. lanthanide
  103255. catalyzed
  103256. enantioselective
  103257. diels-alder
  103258. reacti
  103259. lanthanide
  103260. shift
  103261. reagents
  103262. stereochemical
  103263. analysis
  103264. lanthanides
  103265. lanthanides
  103266. organic
  103267. synthesis
  103268. lanthanoid
  103269. anoid
  103270. triflate
  103271. catalyzed
  103272. conjugate
  103273. addition
  103274. amines
  103275. lanthanum
  103276. lantzsch
  103277. lapachev
  103278. lapidus
  103279. lapidus
  103280. organic
  103281. syntheses
  103282. based
  103283. carbon
  103284. dioxi
  103285. lapointe
  103286. laporterie
  103287. lapouyade
  103288. laramay
  103289. large`
  103290. large
  103291. large
  103292. scale
  103293. preparation
  103294. jacobsen's
  103295. catalyst
  103296. asymmetri
  103297. largeau
  103298. larger
  103299. larger
  103300. rings
  103301. except
  103302. crown
  103303. ethers
  103304. heterophanes
  103305. lariat
  103306. lariat
  103307. ethers
  103308. cation
  103309. complexation
  103310. supramolecular
  103311. lariat
  103312. ethers
  103313. simple
  103314. sidearms
  103315. supramolecular
  103316. systems
  103317. larock
  103318. larock
  103319. applications
  103320. organomercury
  103321. palladium
  103322. larock
  103323. organomercury
  103324. compounds
  103325. organic
  103326. synthesis
  103327. larock
  103328. richard
  103329. palladium
  103330. catalyzed
  103331. vinylic
  103332. substitution
  103333. larouche
  103334. larry
  103335. larsen
  103336. larson
  103337. larson
  103338. richard
  103339. weber
  103340. reaction
  103341. mechanisms
  103342. environ
  103343. lasalle
  103344. laser
  103345. laser
  103346. flash
  103347. photolysis
  103348. studies
  103349. ylide
  103350. forming
  103351. reactions
  103352. laser
  103353. flash
  103354. photolysis
  103355. studies
  103356. ylide-forming
  103357. reactions
  103358. lasic
  103359. lasic
  103360. sterically
  103361. stabilized
  103362. vesicles
  103363. angew
  103364. lasne
  103365. laszlo
  103366. laszlo
  103367. sodium
  103368. spectroscopy
  103369. angewandte
  103370. latchezar
  103371. latent
  103372. later
  103373. lateral
  103374. lathanide
  103375. lathanide
  103376. triflates
  103377. water
  103378. tolerant
  103379. lewis
  103380. acids
  103381. lattes
  103382. lattice
  103383. lattices
  103384. lattrell
  103385. latypova
  103386. laufer
  103387. laufer
  103388. kinetics
  103389. phase
  103390. reactions
  103391. methylene
  103392. launasmaa
  103393. launasmaa
  103394. mauri
  103395. tamminen
  103396. tarja
  103397. tropane
  103398. alkaloids
  103399. launer
  103400. laura
  103401. lauraceae
  103402. laurel
  103403. laurence
  103404. laurencia
  103405. laurencin
  103406. laurent
  103407. laurnnt
  103408. lautens
  103409. lautens
  103410. methods
  103411. control
  103412. multiple
  103413. stereoc
  103414. lautens
  103415. opening
  103416. reactions
  103417. oxabicyclic
  103418. compounds
  103419. lavalle
  103420. lavendamycin
  103421. lavrent'ev
  103422. lawesson
  103423. lawesson's
  103424. lawless
  103425. lawrence
  103426. layerQ
  103427. layered
  103428. lazar
  103429. lazaros
  103430. lazurin
  103431. lazurin
  103432. voronenkov
  103433. osokin
  103434. mechanism
  103435. guillanton
  103436. georges
  103437. electrochemical
  103438. activation
  103439. sulfur
  103440. noble
  103441. chemistry
  103442. compressed
  103443. solutions
  103444. 198019
  103445. tetraacetate
  103446. oxidation
  103447. alkaloid
  103448. synthesis
  103449. leading
  103450. leading
  103451. leads
  103452. leanr
  103453. learned
  103454. least
  103455. leaving
  103456. leazer
  103457. lebedev
  103458. lebedev
  103459. rakhimov
  103460. prokof'ev
  103461. brezgunov
  103462. lebert
  103463. leboeuf
  103464. lebozec
  103465. lecas
  103466. lechtken
  103467. lectins
  103468. lective
  103469. lectka
  103470. lectrophilic
  103471. lectrophilic
  103472. addition
  103473. strained
  103474. olefins
  103475. lectureR
  103476. lederer
  103477. lednicer
  103478. lednicer
  103479. mitscher
  103480. organic
  103481. chemistry
  103482. synthesis
  103483. degenerate
  103484. rearrangements
  103485. triarylvinyl
  103486. cations
  103487. choon
  103488. cross
  103489. interaction
  103490. constants
  103491. transitionstate
  103492. oxidation
  103493. organic
  103494. compounds
  103495. permanganate
  103496. lewis
  103497. photochemistry
  103498. simple
  103499. aldehydes
  103500. buckminsterfullerene
  103501. third
  103502. allotrope
  103503. carbon
  103504. synthetic
  103505. pathways
  103506. cyclobutanones
  103507. advan
  103508. randall
  103509. laibinis
  103510. folkers
  103511. whitesides
  103512. randall
  103513. whitesides
  103514. george
  103515. heterogeneous
  103516. platinum
  103517. chemistry
  103518. orthocyclophanes
  103519. classes
  103520. neoglycoconjugates
  103521. preparation
  103522. appliP
  103523. leete
  103524. leffer's
  103525. leffler
  103526. lefort
  103527. lefrancier
  103528. lefrancier
  103529. lederer
  103530. chemistry
  103531. synthetic
  103532. immunomodulant
  103533. lefrancois
  103534. left--this
  103535. legacy
  103536. leginus
  103537. legitimate
  103538. legler
  103539. legon
  103540. legon
  103541. nature
  103542. ammonium
  103543. methylammonium
  103544. halides
  103545. legrand
  103546. legrand
  103547. rougier
  103548. applications
  103549. optical
  103550. activity
  103551. legzdins
  103552. legzdins
  103553. peter
  103554. veltheer
  103555. electron
  103556. piano
  103557. lehmann
  103558. lehmkuhl
  103559. cryptates
  103560. chemistry
  103561. macropolycyclic
  103562. inclusio
  103563. perspectives
  103564. supramolecular
  103565. chemistry
  103566. molec
  103567. leigh
  103568. leigh
  103569. william
  103570. techniques
  103571. applications
  103572. photoc
  103573. leimgruber
  103574. leinamycin
  103575. leinhos
  103576. leites
  103577. leites
  103578. vibrational
  103579. spectroscopy
  103580. carboranes
  103581. parent
  103582. leitner
  103583. leitner
  103584. walter
  103585. nickel
  103586. complex
  103587. photochemical
  103588. activation
  103589. lelle
  103590. lemenovskii
  103591. lement
  103592. lemer
  103593. lemieux
  103594. lemieux
  103595. human
  103596. blood
  103597. groups
  103598. carbohydrate
  103599. chemistry
  103600. lemieux
  103601. raymond
  103602. explorations
  103603. sugars
  103604. sweet
  103605. lemmen
  103606. lemmen
  103607. richter
  103608. werner
  103609. stumpf
  103610. membe
  103611. length
  103612. lengths
  103613. lengyel
  103614. lengyel
  103615. istvan
  103616. epstein
  103617. irving
  103618. turing
  103619. structures
  103620. simple
  103621. lennart
  103622. lenoir
  103623. lentz
  103624. lentz
  103625. fluorinated
  103626. isocyanides
  103627. ligands
  103628. unusu
  103629. photocycloaddition
  103630. reactions
  103631. conjugated
  103632. enones
  103633. photochemistry
  103634. enamides
  103635. synthesis
  103636. leonard
  103637. leonard
  103638. trimethylene
  103639. bridges
  103640. synthetic
  103641. spacers
  103642. leone
  103643. leone
  103644. mariano
  103645. photochemistry
  103646. heteroatom
  103647. leonid
  103648. leonov
  103649. leont'eva
  103650. leopold
  103651. leowenthal
  103652. leperchec
  103653. lepidoptera
  103654. lepoiure
  103655. lequesne
  103656. lerman
  103657. lerman
  103658. skeletal
  103659. rearrangements
  103660. compounds
  103661. lerner
  103662. leroy
  103663. leslie
  103664. lesser
  103665. lessons
  103666. lester
  103667. letard
  103668. letard
  103669. lapouyade
  103670. rettig
  103671. synthesis
  103672. photophysical
  103673. lethality
  103674. leticia
  103675. letourneau
  103676. leuckart
  103677. leuco
  103678. leucothol
  103679. leuenberger
  103680. leukotrienes
  103681. leukotrienes
  103682. lipoxygenases
  103683. leumann
  103684. leumann
  103685. christian
  103686. developments
  103687. chemistry
  103688. catal
  103689. leval
  103690. levashov
  103691. levashov
  103692. microheterogeneous
  103693. surfactant
  103694. based
  103695. systems
  103696. levchenko
  103697. levin
  103698. levin
  103699. arynes
  103700. reactive
  103701. intermediates
  103702. jones
  103703. levin
  103704. arynes
  103705. reactive
  103706. intermediates
  103707. jones
  103708. levina
  103709. levinson
  103710. levitt
  103711. levkoeva
  103712. levkovskaya
  103713. levoglucosenone
  103714. levoglucosenone
  103715. properties
  103716. reactions
  103717. lichter
  103718. nelson
  103719. carbon
  103720. nuclear
  103721. magnetic
  103722. lichter
  103723. nitrogen
  103724. nuclear
  103725. magnetic
  103726. resonance
  103727. lewars
  103728. lewin
  103729. lewisz
  103730. complexation
  103731. lewis
  103732. catalyzed
  103733. reactions
  103734. lewis
  103735. induced
  103736. alpha
  103737. alkylation
  103738. carbonyl
  103739. cmpds
  103740. lewis
  103741. induced
  103742. alpha-alkylation
  103743. carbonyl
  103744. compounds
  103745. lewis
  103746. promoted
  103747. addition
  103748. reactions
  103749. organometallic
  103750. lewis
  103751. promoted
  103752. diastereoselective
  103753. radical
  103754. cyclization
  103755. lewis
  103756. promoted
  103757. generation
  103758. quinodimethanes
  103759. lewis
  103760. promoted
  103761. tandem
  103762. cycloaddition
  103763. rearrangement
  103764. lewis
  103765. acid-enhanced
  103766. reactivity
  103767. b-unsaturated
  103768. ester
  103769. lewis
  103770. isotope
  103771. effects
  103772. hydrogen
  103773. transfers
  103774. topics
  103775. lewis
  103776. formation
  103777. reactions
  103778. stilbene
  103779. exciplexes
  103780. lewis
  103781. amaryllidaceae
  103782. sceletium
  103783. alkaloids
  103784. natural
  103785. lewis
  103786. muscarine
  103787. oxazole
  103788. imidazole
  103789. thiazole
  103790. peptide
  103791. lewis
  103792. muscarine
  103793. oxazole
  103794. thiazole
  103795. imidazole
  103796. peptide
  103797. lewis
  103798. kenrich
  103799. rethwisch
  103800. david
  103801. catalyzed
  103802. direct
  103803. reactions
  103804. lewis
  103805. norman
  103806. mitchell
  103807. michael
  103808. process
  103809. research
  103810. lewis-acid
  103811. lewis-acid
  103812. catalyzed
  103813. reactions
  103814. lexes
  103815. lexington
  103816. lexitropsins
  103817. lewis
  103818. promoted
  103819. addition
  103820. reactions
  103821. organometallic
  103822. denholm
  103823. thechemistry
  103824. azadirachtin
  103825. natu@
  103826. liaaen
  103827. jensen
  103828. stereochemistry
  103829. naturally
  103830. occurring
  103831. carot@
  103832. lifetime
  103833. ligand
  103834. controlled
  103835. catalysis
  103836. chemo
  103837. stereoselective
  103838. synthes@
  103839. ligand-accelerated
  103840. catalysis
  103841. ligands-discovery@
  103842. linda@
  103843. lingeman@
  103844. lipoxygenases
  103845. lister
  103846. current
  103847. views
  103848. physicochemical
  103849. aspects
  103850. lithiations@
  103851. lithium
  103852. lithium
  103853. perchlorate
  103854. dispersed
  103855. silica
  103856. effic@
  103857. litvinenko
  103858. oleinik
  103859. bifunctional
  103860. catalysis
  103861. lnterscience
  103862. london
  103863. lough@
  103864. lines
  103865. pyrrolo
  103866. ferrocenophanes
  103867. multibridged
  103868. ferrocenophanes@
  103869. makosza
  103870. phase
  103871. reactions@
  103872. salakhov
  103873. ismailov
  103874. maciejewski
  103875. denholm
  103876. thechemistry
  103877. azadirachtin
  103878. norman
  103879. griffith
  103880. marsden
  103881. tetrapropyl
  103882. ammoniv
  103883. synthesis
  103884. chemistry
  103885. insect
  103886. antifeedant
  103887. tricarbonyliron
  103888. lactone
  103889. complexes
  103890. organic
  103891. synthes
  103892. leyerer
  103893. leyva
  103894. leznoff
  103895. leznoff
  103896. insoluble
  103897. polymer
  103898. supports
  103899. general
  103900. lfide
  103901. lgerodt
  103902. lheureux
  103903. organic
  103904. reactions
  103905. aqueous
  103906. media
  103907. focus
  103908. haifang
  103909. noble
  103910. william
  103911. competing
  103912. concepts
  103913. electron
  103914. purdy
  103915. william
  103916. cyclodextrins
  103917. their
  103918. applications
  103919. joullie
  103920. madeleine
  103921. detoxin
  103922. compl
  103923. liaaen
  103924. liaaen
  103925. jensen
  103926. marine
  103927. carotenoids
  103928. marine
  103929. natural
  103930. products
  103931. liaaen
  103932. jensen
  103933. marine
  103934. carotenoids
  103935. selected
  103936. topics
  103937. liaaen
  103938. jensen
  103939. stereochemistry
  103940. naturally
  103941. occurring
  103942. carot
  103943. liaaenjensen
  103944. libf4
  103945. libf4
  103946. lewis
  103947. intramolecular
  103948. diels
  103949. alder
  103950. react
  103951. libman
  103952. library
  103953. lichen
  103954. lichens
  103955. lichtenthaler
  103956. lichtenthaler
  103957. frieder
  103958. fischer's
  103959. proof
  103960. configur
  103961. lichter
  103962. licini
  103963. licio4
  103964. lickiss
  103965. lickiss
  103966. transition
  103967. metal
  103968. complexes
  103969. silylenes
  103970. silen
  103971. licopodium
  103972. lidia
  103973. liebeskind
  103974. liebman
  103975. liebscher~
  103976. liebscher
  103977. aminoalkylheterocycl
  103978. actual
  103979. aspects
  103980. liebscher
  103981. hartmann
  103982. chloro
  103983. propeniminium
  103984. salts
  103985. liesegang
  103986. liesegang
  103987. eyring
  103988. kinetic
  103989. studies
  103990. synthetic
  103991. multid
  103992. lifetime
  103993. lifetime
  103994. lifetime
  103995. dimethylcyclopentane
  103996. biradical
  103997. lifshitz
  103998. lifshitz
  103999. chava
  104000. tropylium
  104001. formation
  104002. toluene
  104003. solution
  104004. ligand
  104005. rolled
  104006. catalysis
  104007. chemo
  104008. stereoselective
  104009. synthes
  104010. ligand
  104011. coupling
  104012. based
  104013. heteroatom
  104014. chemistry
  104015. ligand
  104016. effects
  104017. organometallic
  104018. substitution
  104019. reactions
  104020. ligand
  104021. effects
  104022. rhodium
  104023. catalyzed
  104024. reactions
  104025. ligand
  104026. effects
  104027. chemoselectivity
  104028. transition-metal-c
  104029. ligand
  104030. effects
  104031. stereochemistry
  104032. metalation
  104033. ligand
  104034. influences
  104035. structure
  104036. reactivity
  104037. organoalkal
  104038. ligand-accelerated
  104039. ligand-accelerated
  104040. catalysis
  104041. ligand-accelerated
  104042. catalysis
  104043. ligands
  104044. covery
  104045. ligating
  104046. light
  104047. lightnerx
  104048. lignads
  104049. lignans
  104050. lignans
  104051. neolignans
  104052. related
  104053. compounds
  104054. lignin
  104055. lihren
  104056. lijinsky
  104057. lijinsky
  104058. william
  104059. chemistry
  104060. biology
  104061. nitroso
  104062. compound
  104063. like-selective
  104064. likholobov
  104065. liliana
  104066. lilley
  104067. edward
  104068. photoassociation
  104069. lowest
  104070. triplet
  104071. state
  104072. liming
  104073. limit
  104074. limitations
  104075. limits
  104076. limonoids
  104077. daimay
  104078. colthup
  104079. norman
  104080. fateley
  104081. william
  104082. graselli
  104083. lin'kova
  104084. lincoln
  104085. lincosamine
  104086. indberg
  104087. lindberg
  104088. thomas
  104089. strategies
  104090. tactics
  104091. organic
  104092. synthes
  104093. linde
  104094. lindenbaum
  104095. lindenbaum
  104096. rytting
  104097. sternson
  104098. ionophores
  104099. biological
  104100. lindley
  104101. lindsley
  104102. linear
  104103. linear
  104104. solvation
  104105. energy
  104106. relationships
  104107. improved
  104108. equation
  104109. linearities
  104110. linearly
  104111. linford
  104112. linford
  104113. lorna
  104114. raubenheimer
  104115. helgard
  104116. formation
  104117. reactions
  104118. lingeman
  104119. lingeman
  104120. underberg
  104121. detection
  104122. oriented
  104123. derivatiza
  104124. linkage
  104125. linkages
  104126. linked
  104127. linking
  104128. links
  104129. lintenone
  104130. linti
  104131. lionel
  104132. liotta
  104133. liotta
  104134. application
  104135. macrocyclic
  104136. polydentate
  104137. ligands
  104138. lipase
  104139. lipases
  104140. lipczynska
  104141. lipczynska
  104142. kochany
  104143. photochemistry
  104144. hydroxamic
  104145. acids
  104146. lipid
  104147. lipids
  104148. lipinaM
  104149. lipkowitz
  104150. lipkowitz
  104151. kenny
  104152. peterson
  104153. michael
  104154. molecular
  104155. mechanics
  104156. lipoic
  104157. lipolytic
  104158. lipopeptides
  104159. lipopolysaccharides
  104160. lipoxins
  104161. lipoxins
  104162. related
  104163. eicosanoids
  104164. biosynthesis
  104165. biological
  104166. lipoxygenase
  104167. lipoxygenases
  104168. lipoxygenases
  104169. lippard
  104170. lippert
  104171. lipschutz
  104172. lipschutz
  104173. bhandari
  104174. lindsley
  104175. lipscomb
  104176. lipshutz
  104177. lipshutz
  104178. bruce
  104179. sengupta
  104180. saumitra
  104181. organocopper
  104182. reagents
  104183. lipshutz
  104184. bruce
  104185. evolution
  104186. higher
  104187. order
  104188. cyanocuprates
  104189. liptak
  104190. liptak
  104191. andras
  104192. nanasi
  104193. sztaricskai
  104194. ferenc
  104195. bognar
  104196. rezno
  104197. liquid
  104198. liquid
  104199. crystalline
  104200. ymers
  104201. liquids
  104202. liras
  104203. liska
  104204. liskamp
  104205. liskamp
  104206. application
  104207. modified
  104208. peptides
  104209. liskamp
  104210. conformationally
  104211. restricted
  104212. amino
  104213. acids
  104214. lissi
  104215. lissi
  104216. encinas
  104217. rubio
  104218. singlet
  104219. oxygen
  104220. lister
  104221. lister
  104222. current
  104223. views
  104224. physicochemical
  104225. aspects
  104226. listy
  104227. literature
  104228. literature
  104229. review
  104230. ester
  104231. enolate
  104232. imine
  104233. condensation
  104234. literature
  104235. review
  104236. ester
  104237. enolate
  104238. imine
  104239. condensation
  104240. lithiated
  104241. lithiation
  104242. lithio
  104243. lithio
  104244. diazomethane
  104245. lithio
  104246. trimethylsilyl
  104247. diazomethane
  104248. lithioalkenes
  104249. lithioalkenes
  104250. arylsulphonylhydrazo
  104251. lithioalkoxides
  104252. lithioimidazoles
  104253. lithiomethyl
  104254. lithiooxazolidines
  104255. lithiothiazole
  104256. lithiothiophene
  104257. lithium
  104258. lithium
  104259. lithium
  104260. lithio
  104261. tosylalkanoates
  104262. acylvinyl
  104263. anion
  104264. equival
  104265. lithium
  104266. coordination
  104267. wittig-horner
  104268. reagents
  104269. formed
  104270. lithium
  104271. halocarbenoids
  104272. carbenoids
  104273. synthetic
  104274. versatil
  104275. lithium
  104276. hydride
  104277. lithium
  104278. trimethoxyborohydrid
  104279. comparati
  104280. lithium
  104281. induced
  104282. cyclization
  104283. tetrabenzocyclyne
  104284. novel
  104285. lithium
  104286. perchlorate
  104287. ether
  104288. unusual
  104289. solvent
  104290. lithium
  104291. structure
  104292. sulfones
  104293. sulfoxides
  104294. thioethers
  104295. nitriles
  104296. lithium-1-oxyalkanid
  104297. lithiums
  104298. litina
  104299. litkei
  104300. litkei
  104301. chalcone
  104302. epoxides
  104303. flavonoid
  104304. chemistry
  104305. recent
  104306. little
  104307. little
  104308. daniel
  104309. masjedizadeh
  104310. mohammad
  104311. moeller
  104312. kevin
  104313. litvinenko
  104314. litvinenko
  104315. oleinik
  104316. bifunctional
  104317. catalysis
  104318. litvinov
  104319. litvinovskaya
  104320. laser
  104321. flash
  104322. photolysis
  104323. studies
  104324. hydrogen
  104325. migrati
  104326. lived
  104327. lively
  104328. liver
  104329. livia
  104330. living
  104331. livinghouse
  104332. livingston
  104333. livingston
  104334. douglas
  104335. application
  104336. silicon
  104337. chemistry
  104338. livingstone\
  104339. livingstone
  104340. bicarbocyclic
  104341. natural
  104342. products
  104343. second
  104344. suppleme\
  104345. lization
  104346. lizines
  104347. lkylations
  104348. lkylations
  104349. nonstabilized
  104350. carbanions
  104351. llewellyn
  104352. lloyd
  104353. lloyd
  104354. douglas
  104355. mcnab
  104356. hamish
  104357. dihydro
  104358. diazepines
  104359. lloyd
  104360. williams
  104361. albericio
  104362. fernando
  104363. giralt
  104364. ernest
  104365. converg
  104366. lly-active
  104367. lmidazoles
  104368. lndazol
  104369. lnduced
  104370. lnterscience
  104371. lnterscience
  104372. lobach
  104373. lobach
  104374. kormer
  104375. insertion
  104376. diene
  104377. hydrocarbons
  104378. lobanov
  104379. lobes
  104380. local
  104381. localized
  104382. lockhart
  104383. lockhoff
  104384. lockhoff
  104385. oswald
  104386. glycolipids
  104387. immunomodulators
  104388. synthesis
  104389. lodder
  104390. loderer
  104391. lodine
  104392. loening
  104393. loening
  104394. merritt
  104395. later
  104396. wright
  104397. polynuclear
  104398. aromatic
  104399. loewenthal
  104400. logal
  104401. logic
  104402. logical
  104403. lohberger
  104404. lohray
  104405. lohray
  104406. bhushan
  104407. vidya
  104408. oxazaborolidines
  104409. dioxaboroli
  104410. lohray
  104411. cyclic
  104412. sulfites
  104413. cyclic
  104414. sulfates
  104415. epoxide
  104416. lohray
  104417. recent
  104418. advances
  104419. asymmetric
  104420. dihydroxylat
  104421. lokteev
  104422. lolita
  104423. lomakina
  104424. lombardino
  104425. lombardino
  104426. kuhla
  104427. benzothiazines
  104428. relate
  104429. londonT
  104430. london
  104431. roles
  104432. silver
  104433. salts
  104434. organic
  104435. processes
  104436. range
  104437. interact
  104438. cyclopropyl
  104439. groups
  104440. carbonium
  104441. long-lived
  104442. long-lived
  104443. cyclopropylcarbinyl
  104444. cations
  104445. long-range
  104446. longifolene
  104447. fotsch
  104448. christopher
  104449. enzyme
  104450. cataly
  104451. palladium
  104452. catalyzes
  104453. looks
  104454. lopez
  104455. lophanes
  104456. lopusinski
  104457. lorenz
  104458. lorna
  104459. loschmidt
  104460. butyloxycarbonyl
  104461. protecting
  104462. group
  104463. under
  104464. lough
  104465. loughlin
  104466. louis
  104467. lounasmaa
  104468. lounasman
  104469. loupy
  104470. loupy
  104471. tchoubar
  104472. effects
  104473. organic
  104474. organometalli
  104475. loupy
  104476. andre
  104477. tchoubar
  104478. bianka
  104479. astruc
  104480. didier
  104481. effects
  104482. resul
  104483. lourdes
  104484. lovelace
  104485. coordinate
  104486. carbene
  104487. complexes
  104488. nickel
  104489. platinum
  104490. valent
  104491. tantalum
  104492. mediated
  104493. reaction
  104494. low-coordinate
  104495. low-coordinate
  104496. hypervalent
  104497. phosphorus
  104498. low-coordinated
  104499. low-temperature
  104500. low-temperature
  104501. tandem
  104502. enyne
  104503. allene
  104504. radical
  104505. cyclizations
  104506. low-v
  104507. low-valent
  104508. low-valent
  104509. ruthenium
  104510. complexes
  104511. lewis
  104512. acids
  104513. catalysts
  104514. lower
  104515. lowest
  104516. william
  104517. discovery
  104518. development
  104519. anthracycline
  104520. william
  104521. targeting
  104522. minorgroove
  104523. control
  104524. lowrey
  104525. lozac'h
  104526. lozac'h
  104527. goodson
  104528. powell
  104529. nodal
  104530. nomenclature
  104531. general
  104532. lozac'h
  104533. stavaux
  104534. dithiolium
  104535. lozac'h
  104536. facts
  104537. words
  104538. heteroatomic
  104539. nomenclature
  104540. lozach
  104541. lozinskii
  104542. lsoprenoids
  104543. jiang
  104544. construction
  104545. alpha
  104546. alkyliden
  104547. lubben
  104548. lubineauu
  104549. lubineau
  104550. queneau
  104551. water
  104552. promoted
  104553. organic
  104554. reactionsu
  104555. lucchi
  104556. lucchini
  104557. luche
  104558. lucia
  104559. luciferase
  104560. lucio
  104561. lucjan
  104562. ludek
  104563. ludger
  104564. wolfgang
  104565. keese
  104566. reinhart
  104567. planarizing
  104568. distortions
  104569. luening
  104570. luening
  104571. ulrich
  104572. baumstark
  104573. roland
  104574. wangnic
  104575. carsten
  104576. mueller
  104577. luffariolide
  104578. luffariolide
  104579. lugade
  104580. lugtenburg
  104581. synthetic
  104582. applications
  104583. dithioacetal
  104584. tsung
  104585. silyl
  104586. substituted
  104587. conjugated
  104588. luigi
  104589. luk'yanov
  104590. luk'yanova
  104591. lukacs
  104592. lukacs
  104593. gabor
  104594. recent
  104595. progress
  104596. chemical
  104597. synthesis
  104598. lukehart
  104599. lukehart
  104600. metalla
  104601. diketones
  104602. their
  104603. derivatives
  104604. 19811
  104605. lukevics
  104606. lukevics
  104607. edmunds
  104608. zablocka
  104609. nucleoside
  104610. synthesis
  104611. organosi
  104612. lukevits
  104613. luknitskii
  104614. luminescence
  104615. luminescent
  104616. henning
  104617. baizer
  104618. manuel
  104619. organic
  104620. electrochemistry
  104621. lundstedt
  104622. lundstrom
  104623. lusztyk
  104624. lutomski
  104625. lutsenko
  104626. lutsenko
  104627. proskurnina
  104628. organic
  104629. phosphorus
  104630. compounds
  104631. luzzio
  104632. lwowski
  104633. lwowski
  104634. nitrenes
  104635. reactive
  104636. intermediates
  104637. jones
  104638. lwowski
  104639. nitrenes
  104640. reactive
  104641. intermediates
  104642. jones
  104643. lyapina
  104644. lyapina
  104645. lygin
  104646. ulendeeva
  104647. mechanism
  104648. adsorpt
  104649. lycopodium
  104650. lycoricidine
  104651. lycorine
  104652. lycorines
  104653. lygin
  104654. lymer
  104655. lymphocyte
  104656. lynch
  104657. lyndsay
  104658. lyngbya
  104659. lyotropic
  104660. lysed
  104661. lysergene
  104662. lysergic
  104663. lythgoe
  104664. lythgoe
  104665. synthetic
  104666. approaches
  104667. vitamin
  104668. relative
  104669. lythraceae
  104670. lythraceous
  104671. lytic
  104672. lyubovskaya
  104673. lyzwa
  104674. steric
  104675. effects
  104676. rocha
  104677. pyrroloquinolines
  104678. pyrrolo
  104679. rocha
  104680. pyrroloquinolines
  104681. pyrrolo
  104682. rocha
  104683. pyrroloquinolines
  104684. pyrrolo
  104685. groen
  104686. zeelen
  104687. steroid
  104688. rubin
  104689. chemistry
  104690. vicinal
  104691. glucosinolates
  104692. 49197
  104693. applied
  104694. chemistry
  104695. bersohn
  104696. esack
  104697. computers
  104698. lasne
  104699. ripoll
  104700. synthesis
  104701. synthetic
  104702. cerny
  104703. stanek
  104704. anhydro
  104705. derivatives
  104706. aldohexose
  104707. whistler
  104708. metabolism
  104709. fructose
  104710. christl
  104711. cycloadditions
  104712. crobial
  104713. polisaccharides
  104714. approaches
  104715. cohen
  104716. angew
  104717. photochemistry
  104718. demuth
  104719. synthesis
  104720. natural
  104721. ephritikhine
  104722. activation
  104723. alkane
  104724. farona
  104725. homogeneous
  104726. catalysis
  104727. arene
  104728. group
  104729. tricarbo
  104730. ferrocenophanes
  104731. multibridged
  104732. ferrocenophanes
  104733. follet
  104734. complexes
  104735. diborane
  104736. follet
  104737. london
  104738. complexes
  104739. dibora
  104740. elnagdi
  104741. elgemie
  104742. elaal
  104743. heterocycles
  104744. hatanaka
  104745. nitta
  104746. ishimaru
  104747. osaka
  104748. bruce
  104749. cyclometalation
  104750. reactions
  104751. angewandte
  104752. aroney
  104753. electro
  104754. optical
  104755. effect
  104756. conformational
  104757. broadhurst
  104758. hassall
  104759. thomas
  104760. london
  104761. miller
  104762. hydroxamate
  104763. approach
  104764. julia
  104765. recent
  104766. advances
  104767. double
  104768. karpf
  104769. angew
  104770. 0rganic
  104771. synthesis
  104772. lalonde
  104773. synthesis
  104774. organosilic
  104775. green
  104776. spectrometry
  104777. stereochemistry
  104778. organ
  104779. madesclair
  104780. tetrahedron
  104781. synthesis
  104782. sulfoxide
  104783. madesclaire
  104784. tetrahedron
  104785. synthesis
  104786. sulfoxid
  104787. makosza
  104788. phase
  104789. reactions
  104790. narita
  104791. pittman
  104792. synthesis
  104793. preparation
  104794. neuenschwander
  104795. synthetic
  104796. novel
  104797. polycyclic
  104798. conjugated
  104799. levinson
  104800. tetrahedron
  104801. thionatio
  104802. doyle
  104803. electrophilic
  104804. metal
  104805. carbe
  104806. doyle
  104807. catalytic
  104808. methods
  104809. metal
  104810. platz
  104811. tetrahedron
  104812. recent
  104813. aspects
  104814. carbene
  104815. porter
  104816. vulcanization
  104817. rubber
  104818. organic
  104819. chemistry
  104820. sulfur
  104821. bryce
  104822. aldrichimica
  104823. tetrathiafulvalenes
  104824. euerby
  104825. waigh
  104826. hillier
  104827. rabinovitz
  104828. cohen
  104829. halpern
  104830. angew
  104831. regitz
  104832. angew
  104833. chemistry
  104834. phosphor
  104835. reuman
  104836. meyers
  104837. tetrahedron
  104838. syntheti
  104839. rosenblum
  104840. organomet
  104841. chemistry
  104842. salakhov
  104843. ismailov
  104844. sainsbury
  104845. synthesis
  104846. pyrido
  104847. carbazoles
  104848. semmelhack
  104849. tetrahedron
  104850. application
  104851. newer
  104852. reetz
  104853. dyotropic
  104854. rearrangements
  104855. related
  104856. exchange
  104857. tisler
  104858. proced
  104859. synthetic
  104860. approaches
  104861. tsutsui
  104862. courtney
  104863. sigma
  104864. rearrangements
  104865. organotr
  104866. vandewalle
  104867. clercq
  104868. tetrahedron
  104869. yalpani
  104870. tetrahedron
  104871. survey
  104872. recent
  104873. advanc
  104874. yandewalle
  104875. declercq
  104876. tetrahedron
  104877. total
  104878. zaoral
  104879. listy
  104880. peptide
  104881. synthesis
  104882. m-bond
  104883. maaato
  104884. maatman
  104885. maatman
  104886. density
  104887. entropy
  104888. criteria
  104889. identifying
  104890. mabry
  104891. macdermott
  104892. macdonald
  104893. macdonell
  104894. machine
  104895. machinery
  104896. maciejewski
  104897. maciejewski
  104898. maciejewski
  104899. andrzej
  104900. steer
  104901. ronald
  104902. photophysics
  104903. physical
  104904. mackay
  104905. mackie
  104906. mackie
  104907. desulphurization
  104908. phosphorus
  104909. reagents
  104910. mackie
  104911. functional
  104912. group
  104913. conversions
  104914. using
  104915. phosphorus
  104916. mackiewicz
  104917. mackiewicz
  104918. furstoss
  104919. amidyl
  104920. radicals
  104921. structure
  104922. reacti
  104923. maclean
  104924. maclean
  104925. synthesis
  104926. biosynthesis
  104927. spirobenzylisoquin
  104928. macnicol
  104929. macomber
  104930. macquarrie
  104931. macro
  104932. macroacyclic
  104933. macrocycle
  104934. macrocycles
  104935. macrocyclic
  104936. macrocyclic
  104937. chemistry
  104938. aspects
  104939. organic
  104940. inorganic
  104941. supra
  104942. macrocyclic
  104943. imides
  104944. versatile
  104945. synthons
  104946. enlargement
  104947. macrocyclic
  104948. lactones
  104949. dirhodium
  104950. catalyzed
  104951. intramolecu
  104952. macrocyclic
  104953. polyamines
  104954. intelligent
  104955. functions
  104956. macrocyclic
  104957. trichothecenes
  104958. macrocyclisation
  104959. macrocyclization
  104960. macroexpansion
  104961. macroexpansion
  104962. methodology
  104963. synthesis
  104964. medium
  104965. rings
  104966. macroheterocycles
  104967. macroheterocyclic
  104968. macrolactamization
  104969. macrolactone
  104970. macrolide
  104971. macrolides
  104972. recent
  104973. progress
  104974. chemistry
  104975. biochemistry
  104976. macromol
  104977. macromole
  104978. macromolecular
  104979. macromolecular
  104980. materials
  104981. introduction
  104982. macromolecules
  104983. macromycetes
  104984. macronecine
  104985. macropolycyclic
  104986. macrocyclic
  104987. chemistry
  104988. aspects
  104989. organic
  104990. inorganic
  104991. supra@
  104992. macrolides@
  104993. macropolycyclic
  104994. magnesium
  104995. compounds
  104996. classification
  104997. analysis
  104998. crystallo@
  104999. makes@
  105000. makosza@
  105001. mamanuthaquinone@
  105002. manganese
  105003. acetate
  105004. initiated
  105005. oxidative
  105006. radical
  105007. react@
  105008. mannschreck@
  105009. marcetta@
  105010. margaretha
  105011. marine
  105012. pyridoacridine
  105013. alkaloids
  105014. structure
  105015. synthesis
  105016. biol@
  105017. markus@
  105018. martin
  105019. maryanoff
  105020. oxazoles
  105021. oxazolines
  105022. organic
  105023. synthesis
  105024. masked@
  105025. masuyama
  105026. yoshiro
  105027. palladium
  105028. catalyzed
  105029. carbonyl
  105030. allylation
  105031. mathur
  105032. narang
  105033. williams
  105034. polymers
  105035. organ@
  105036. maury@
  105037. mcardle
  105038. mckervey
  105039. synthetic
  105040. approaches
  105041. large
  105042. diamondoid
  105043. hydroc@
  105044. mcomie
  105045. recent
  105046. developments
  105047. protecting
  105048. groups
  105049. 1979@
  105050. measurements@
  105051. mechanism
  105052. mechanism
  105053. homogeneous
  105054. hydrogenation@
  105055. emical
  105056. decomposition
  105057. macropolycyclic
  105058. macropolycyclic
  105059. polyethers
  105060. cages
  105061. related
  105062. compounds
  105063. macrostructure
  105064. madaligar
  105065. madeleine
  105066. mader
  105067. madesclair
  105068. madesclaire
  105069. madeselaire
  105070. madhav
  105071. madix
  105072. madix
  105073. reaction
  105074. kinetics
  105075. mechanism
  105076. metal
  105077. single
  105078. madix
  105079. surface
  105080. reactivity
  105081. heterogeneous
  105082. reactions
  105083. madsen
  105084. maekawa
  105085. maercker
  105086. magarajan
  105087. magarajan
  105088. dibenzoxazepines
  105089. chemistry
  105090. biological
  105091. activi
  105092. magdolna
  105093. magellanine
  105094. magellaninone
  105095. magerlein
  105096. maghar
  105097. magic
  105098. magid
  105099. magid
  105100. nucleophilic
  105101. organometallic
  105102. displacement
  105103. react
  105104. magnesium
  105105. magnesium
  105106. calcium
  105107. strontium
  105108. barium
  105109. magnesium
  105110. compounds
  105111. classification
  105112. analysis
  105113. crystallo
  105114. magnetic
  105115. magnetic
  105116. properties
  105117. aromatic
  105118. transition
  105119. states
  105120. diels
  105121. magnetism
  105122. magnus
  105123. magnus
  105124. organosilicon
  105125. reactions
  105126. carbon
  105127. carbon
  105128. magnus
  105129. philip
  105130. general
  105131. strategy
  105132. using
  105133. acetylene
  105134. magnusson
  105135. mague
  105136. maguire
  105137. magyar
  105138. mahadevan
  105139. mahatoX
  105140. mahato
  105141. glycosides
  105142. saponins
  105143. sapogenins
  105144. second
  105145. supplemX
  105146. mahidol
  105147. mahidol
  105148. sahakitpichan
  105149. ruchirawat
  105150. bioactive
  105151. natural
  105152. mahmoud
  105153. maier
  105154. maillard
  105155. group
  105156. metallocenes
  105157. substituted
  105158. cyclopentadienyl
  105159. group
  105160. organometallics
  105161. synthesis
  105162. lyndsay
  105163. nicholson
  105164. brian
  105165. orthoman
  105166. ganated
  105167. ketones
  105168. main-group
  105169. main-group
  105170. metallocenes
  105171. recent
  105172. developments
  105173. maintenance
  105174. mairanovskii
  105175. mairanovskii
  105176. electroreduction
  105177. organic
  105178. compounds
  105179. maire
  105180. maiti
  105181. maitland
  105182. maitlis
  105183. maitlis
  105184. pentamethylcyclopent
  105185. rhodium
  105186. iridium
  105187. complex
  105188. maizus
  105189. majectic
  105190. majetich
  105191. major
  105192. majoral
  105193. majoral
  105194. synthesis
  105195. reactions
  105196. heterocyclic
  105197. compound
  105198. majuscula
  105199. makela
  105200. makhametsin
  105201. makhluf
  105202. makhon'kov
  105203. makin
  105204. making
  105205. making
  105206. molecules
  105207. order
  105208. making
  105209. pharmaceuticals
  105210. homogeneous
  105211. catalysis
  105212. makino
  105213. makosza
  105214. makosza
  105215. reactions
  105216. carbanions
  105217. halogenocarbons
  105218. makosza
  105219. phase
  105220. reactions
  105221. organic
  105222. chemistry
  105223. survey
  105224. makoto
  105225. maksimenko
  105226. maksimova
  105227. malcolm
  105228. maleate
  105229. maleates
  105230. maleic
  105231. malek
  105232. malenfant
  105233. maletina
  105234. maletina
  105235. mironova
  105236. yagupolskii
  105237. arylperfl
  105238. malhotra
  105239. malic
  105240. malignant
  105241. maliverney
  105242. malkin
  105243. malkin
  105244. jacob
  105245. photophysical
  105246. photochemical
  105247. properties
  105248. mallory
  105249. malloy
  105250. malloy
  105251. bauman
  105252. carreira
  105253. conformational
  105254. barrier
  105255. malonaldehyde
  105256. malonate
  105257. malonates
  105258. malone
  105259. malonodinitrile
  105260. malononitrile
  105261. malonylvinyl
  105262. malowsky
  105263. malowsky
  105264. synthesis
  105265. structure
  105266. vibrational
  105267. spectr
  105268. malysheva
  105269. mamaev
  105270. mamanuthaquinone
  105271. mamdouh
  105272. mames
  105273. mammalian
  105274. mammals
  105275. manabe
  105276. managing
  105277. manas
  105278. mancuso
  105279. mancuso
  105280. swern
  105281. activated
  105282. dimethyl
  105283. sulfoxide
  105284. useful
  105285. mandal
  105286. mandel'shtam
  105287. mandelates
  105288. mandelbaum
  105289. mandelbaum
  105290. application
  105291. spectrometry
  105292. stereochemi
  105293. mander
  105294. mander
  105295. lewis
  105296. exploitation
  105297. synthons
  105298. synthesi
  105299. mander
  105300. lewis
  105301. chemistry
  105302. gibberellins
  105303. overview
  105304. mandolini
  105305. mandon
  105306. mandrichenko
  105307. manecke
  105308. manecke
  105309. storck
  105310. polymeric
  105311. cntalysts
  105312. 197817
  105313. angewandte
  105314. manelis
  105315. manesium
  105316. manfred
  105317. manfrin
  105318. manganeseG
  105319. manganese
  105320. acetate
  105321. initiated
  105322. oxidative
  105323. radical
  105324. react
  105325. manganese
  105326. based
  105327. asymmetric
  105328. oxidative
  105329. free-radical
  105330. cycliz
  105331. manganese
  105332. mediated
  105333. reactions
  105334. unsaturated
  105335. systems
  105336. manganese
  105337. salen
  105338. catalyzed
  105339. asymmetric
  105340. epoxidation
  105341. conjugatG
  105342. manganese-mediated
  105343. mangeney
  105344. mangold
  105345. mangold
  105346. synthesis
  105347. biosynthesis
  105348. alkoxylipids
  105349. manhas
  105350. manifestation
  105351. manipulation
  105352. manipulations
  105353. mannich
  105354. mannich
  105355. biscyclizations
  105356. total
  105357. synthesis
  105358. ajmalicine
  105359. mannich
  105360. reactions
  105361. carbonyl
  105362. compounds
  105363. enamines
  105364. mannitol
  105365. manno
  105366. mannojirimycin
  105367. mannonolactam
  105368. mannopyranosides
  105369. mannopyranosyl
  105370. mannose
  105371. mannosidase
  105372. mannostatin
  105373. mannostatin
  105374. derivatives
  105375. family
  105376. glycoprotein
  105377. mannschreck
  105378. mannschreck
  105379. albrecht
  105380. chiroptical
  105381. detection
  105382. during
  105383. liquid
  105384. manoalide
  105385. manojlovicmuir
  105386. manov
  105387. manov
  105388. yuvenskii
  105389. nefedov
  105390. synthesis
  105391. nitrogen
  105392. contai
  105393. mansfield
  105394. mansilla
  105395. manske
  105396. mansour
  105397. mansuri
  105398. mansuy
  105399. mantsch
  105400. manual
  105401. manuel
  105402. manuela
  105403. manufacture
  105404. manufacturing
  105405. manuilov
  105406. many-member
  105407. manzamine
  105408. manzocchi
  105409. mar'in
  105410. maracek
  105411. maragarita
  105412. maramatsu
  105413. marcaccini
  105414. marcaccini
  105415. torroba
  105416. isocyanides
  105417. heterocycli
  105418. marcel
  105419. marcell
  105420. marcelo
  105421. marcetta
  105422. march
  105423. march
  105424. jerry
  105425. advanced
  105426. organic
  105427. chemistry
  105428. wiley
  105429. marchamd
  105430. marchamd
  105431. polycyclic
  105432. compounds
  105433. intermediates
  105434. marchand]
  105435. marchand
  105436. polycarbocyclic
  105437. bridged
  105438. compounds
  105439. second
  105440. marchand
  105441. polycyclic
  105442. compounds
  105443. intermediates
  105444. marchetti
  105445. marcial
  105446. marciniec
  105447. marciniec
  105448. bogdan
  105449. comprehensive
  105450. handbook
  105451. hydro
  105452. silylati
  105453. marcinow
  105454. marco
  105455. marcos
  105456. marcus
  105457. marcus
  105458. properties
  105459. organic
  105460. liquids
  105461. relevant
  105462. mardykin
  105463. mardykin
  105464. gaponik
  105465. popov
  105466. etherates
  105467. organoal
  105468. marechal
  105469. marek
  105470. maretina
  105471. maretina
  105472. synthetic
  105473. aspects
  105474. chemistry
  105475. maretina
  105476. synthetic
  105477. aspects
  105478. chemistry
  105479. unsaturat
  105480. margaret
  105481. margaretha
  105482. margaretha
  105483. margarita
  105484. margolin
  105485. margolin
  105486. alexey
  105487. enzymes
  105488. chemtech
  105489. maria
  105490. mariaj
  105491. marian
  105492. mariani
  105493. marianne
  105494. mariano
  105495. marie
  105496. mariella
  105497. marietta
  105498. marina
  105499. marine
  105500. marine
  105501. carotenoids-selected
  105502. topics
  105503. marine
  105504. metabolites
  105505. metal
  105506. chelation
  105507. facts
  105508. marine
  105509. nitrogen-containing
  105510. heterocyclic
  105511. natural
  105512. products
  105513. marine
  105514. pyridoacridine
  105515. alkaloids
  105516. structure
  105517. synthesis
  105518. marine
  105519. sterols
  105520. marinetti
  105521. marino
  105522. marino
  105523. asymmetric
  105524. synthesis
  105525. optically
  105526. active
  105527. vinyl
  105528. mario
  105529. marion
  105530. marisa
  105531. herman
  105532. small
  105533. molecules
  105534. large
  105535. century
  105536. progr
  105537. markaryan
  105538. marked
  105539. markgraf
  105540. markham
  105541. marki
  105542. markies
  105543. markies
  105544. peter
  105545. akkerman
  105546. bickelhaupt
  105547. friedrich
  105548. smeets
  105549. marko
  105550. markov
  105551. markovskii
  105552. markovskii
  105553. kalchenko
  105554. negrebetskii
  105555. amidine
  105556. deriva
  105557. markovsky
  105558. markovsky
  105559. leonid
  105560. penkovsky
  105561. vladimir
  105562. shermolovich
  105563. marks
  105564. marks
  105565. spectroscopy
  105566. organoiron
  105567. compounds
  105568. organ
  105569. marks
  105570. tobin
  105571. surface
  105572. bound
  105573. metal
  105574. hydrocarbyls
  105575. organometalli
  105576. markus
  105577. marlin
  105578. marlow
  105579. marlow
  105580. perkyns
  105581. pettitt
  105582. montgomery
  105583. effec
  105584. marotta
  105585. marquarding
  105586. marquardt
  105587. marquet
  105588. marsais
  105589. marsdenv
  105590. marshall
  105591. marshall
  105592. trans
  105593. cycloalkenes
  105594. betweenanenes
  105595. molecu
  105596. marshall
  105597. james
  105598. chiral
  105599. alkoxyallylic
  105600. allenic
  105601. stannanes
  105602. marshall
  105603. caruthers
  105604. phosphorodithioate
  105605. poten
  105606. marson
  105607. marson
  105608. charles
  105609. reactions
  105610. carbonyl
  105611. compounds
  105612. monoha
  105613. marston
  105614. marston
  105615. hostettmann
  105616. modern
  105617. separation
  105618. methods
  105619. natural
  105620. marston
  105621. hostettmann
  105622. modern
  105623. sepnration
  105624. methods
  105625. marta
  105626. martelli
  105627. martens
  105628. martin
  105629. martin
  105630. martin
  105631. arnold
  105632. youhua
  105633. palladium
  105634. catalyzed
  105635. cross
  105636. coupli
  105637. martin
  105638. bauer
  105639. pankratov
  105640. cyclotrimerization
  105641. cyano
  105642. martin
  105643. michael
  105644. linda
  105645. james
  105646. novel
  105647. pyridodiind
  105648. martin
  105649. robert
  105650. fries
  105651. rearrangement
  105652. prepar
  105653. martin
  105654. methodology
  105655. construction
  105656. quaternary
  105657. martin
  105658. synthesis
  105659. aldehydes
  105660. ketones
  105661. carboxylic
  105662. martin
  105663. stephen
  105664. guinn
  105665. denise
  105666. prelog
  105667. djerassi
  105668. lactonic
  105669. martinek
  105670. martinez
  105671. martino
  105672. martynov
  105673. maruoka
  105674. maruyama
  105675. marvaud
  105676. marvell
  105677. marvell
  105678. thermal
  105679. electrocyclic
  105680. reactions
  105681. organic
  105682. chemistr
  105683. marvin
  105684. maryanoff
  105685. maryanoff
  105686. hutchins
  105687. maryanoff
  105688. stereochemical
  105689. maryanoff
  105690. oxazoles
  105691. oxazolines
  105692. organic
  105693. synthesis
  105694. maryanoff
  105695. oxazoles
  105696. oxazolines
  105697. organic
  105698. synthesis
  105699. maryanoff
  105700. spectroscopic
  105701. properties
  105702. oxazoles
  105703. marye
  105704. marygail
  105705. marzilli
  105706. marzorati
  105707. masaaki
  105708. masad
  105709. masahide
  105710. masahiro
  105711. masahka
  105712. masaji
  105713. masakatsu
  105714. masaki
  105715. masamatsu
  105716. masami
  105717. masamune
  105718. masamune
  105719. recent
  105720. progress
  105721. macrolide
  105722. synthesis
  105723. masanao
  105724. masao
  105725. masaru
  105726. masataka
  105727. masato
  105728. masatomo
  105729. masaya
  105730. masayoshi
  105731. masazumi
  105732. mascal
  105733. mascal
  105734. noncovalent
  105735. design
  105736. principles
  105737. synthe
  105738. mascaretti
  105739. eugene
  105740. stereocontrolled
  105741. manipulations
  105742. chromatograp
  105743. mashkina
  105744. mashkina
  105745. catalytic
  105746. synthesis
  105747. sulfides
  105748. sulfoxides
  105749. masihito
  105750. masiukiewicz
  105751. masjedizadeh
  105752. masked
  105753. maskill
  105754. maslak
  105755. maslak
  105756. przemyslaw
  105757. fragmentations
  105758. photoinduced
  105759. electron
  105760. maslov
  105761. mason
  105762. mason
  105763. tertiary
  105764. phosphine
  105765. ligands
  105766. organometalli
  105767. mason
  105768. stephen
  105769. prebiotic
  105770. sources
  105771. biomolecular
  105772. handedness
  105773. mason
  105774. sonochemistry
  105775. ultrasound
  105776. chemist
  105777. massachusetts
  105778. massey
  105779. massimo
  105780. massiot
  105781. massy
  105782. masters
  105783. masters
  105784. fischer
  105785. tropsch
  105786. reaction
  105787. 197817
  105788. advances
  105789. mastryukov
  105790. mastryukova
  105791. mastryukova
  105792. kabachnik
  105793. enolization
  105794. phosphoryl
  105795. masuda
  105796. masuda
  105797. tachimori
  105798. design
  105799. synthesis
  105800. properties
  105801. masunov
  105802. masuo
  105803. masuyama
  105804. masuyama
  105805. yoshiro
  105806. palladium
  105807. catalyzed
  105808. carbonyl
  105809. allylation
  105810. mataga
  105811. mataga
  105812. noboru
  105813. photoinduced
  105814. electron
  105815. transfer
  105816. multiple
  105817. matalloporphyrin-cat
  105818. matasi
  105819. matched
  105820. matchings
  105821. mateo
  105822. material
  105823. materials
  105824. mathey
  105825. mathey
  105826. francois
  105827. decade
  105828. research
  105829. phosphin
  105830. imine
  105831. chemi
  105832. mathey
  105833. francois
  105834. expanding
  105835. analogy
  105836. between
  105837. phosphorus
  105838. mathey
  105839. francois
  105840. marinetti
  105841. angela
  105842. mercier
  105843. francois
  105844. synthesis
  105845. mathias
  105846. mathias
  105847. esterification
  105848. alkylation
  105849. reactions
  105850. employin
  105851. mathias
  105852. synthetic
  105853. applications
  105854. isoureas
  105855. mathieu
  105856. mathieu
  105857. weill
  105858. raynal
  105859. formation
  105860. bonds
  105861. introduction
  105862. mathur
  105863. mathur
  105864. narang
  105865. williams
  105866. polymers
  105867. organ
  105868. matnishyan
  105869. matrice
  105870. matrices
  105871. matrix
  105872. matrixes
  105873. matros
  105874. matson
  105875. matsubayashi
  105876. matsuda
  105877. matsueda
  105878. matsui
  105879. matsumoto
  105880. matsumoto
  105881. uchida
  105882. acheson
  105883. synthesis
  105884. reactions
  105885. matsumoto
  105886. kiyoshi
  105887. acheson
  105888. morrin
  105889. organic
  105890. synthesis
  105891. matsunaga
  105892. matsuo
  105893. matsushita
  105894. matsuura
  105895. mattay
  105896. mattes
  105897. matteson
  105898. matthew
  105899. matthias
  105900. matthijs
  105901. maturing
  105902. matusiak
  105903. matveev
  105904. matveev
  105905. gorbatenko
  105906. samarai
  105907. dihaloalkyl
  105908. heter
  105909. matveeva
  105910. matyska
  105911. mauder
  105912. mauger
  105913. mauri
  105914. maurice
  105915. maurilio
  105916. maurizio
  105917. mauro
  105918. maury
  105919. mautner
  105920. mavrov
  105921. maximilian
  105922. maximum
  105923. maxtell
  105924. mayer
  105925. mayer
  105926. reflections
  105927. carotenoid
  105928. synthesis
  105929. mayer
  105930. james
  105931. stretch
  105932. isomers
  105933. artifact
  105934. butcher
  105935. trumper
  105936. microscale
  105937. techniq
  105938. andreas
  105939. hoffmaiester
  105940. recent
  105941. advances
  105942. chemis
  105943. scales
  105944. nucleophilicity
  105945. electrophilicity
  105946. herbert
  105947. baran
  105948. janusz
  105949. heigl
  105950. ulrich
  105951. 334455
  105952. hexamethyl12
  105953. maytansinoids
  105954. mazur
  105955. mazur
  105956. mandrichenko
  105957. katkevich
  105958. methods
  105959. synthesi
  105960. mazzieri
  105961. mazzocchi
  105962. mazzocchi
  105963. photochemistry
  105964. imides
  105965. organic
  105966. mazzola
  105967. mazzucato
  105968. mazzucato
  105969. momicchioli
  105970. fabio
  105971. rotational
  105972. isomerism
  105973. mcadam
  105974. mcadoo
  105975. mcadoo
  105976. davidj
  105977. morton
  105978. thomas
  105979. hellman
  105980. phase
  105981. analogs
  105982. mcardle
  105983. mcardle
  105984. mcbride
  105985. mccamley
  105986. mccarthy
  105987. mcclelland
  105988. mccloskey
  105989. mccombie
  105990. mccombie
  105991. stuart
  105992. ortiz
  105993. claudio
  105994. brian
  105995. ganguly
  105996. ashit
  105997. mccomsey
  105998. mccord
  105999. mccown
  106000. mccoy
  106001. mccullough
  106002. mccullough
  106003. xylylenes
  106004. isoindenes
  106005. reaction
  106006. interm
  106007. mcdaniel
  106008. mcdermott
  106009. mcdonagh
  106010. mcdonald
  106011. mcdowell
  106012. mcelvain
  106013. mcelvany
  106014. mcelvany
  106015. stephen
  106016. callahan
  106017. characterizat
  106018. mcgarvey
  106019. mcgill
  106020. mcglinchey
  106021. mcglinchey
  106022. michael
  106023. slowed
  106024. tripodal
  106025. rotation
  106026. arene
  106027. chrom
  106028. mcgovern
  106029. mcgovern
  106030. patricia
  106031. vollhardt
  106032. peter
  106033. synthesis
  106034. mcgrath
  106035. mcgregor
  106036. mcgregor
  106037. william
  106038. sherrington
  106039. david
  106040. recent
  106041. synthetic
  106042. mcinnis
  106043. mckean
  106044. mckee
  106045. mckeever
  106046. mckelvey
  106047. mckervey
  106048. mckervey
  106049. anthony
  106050. bohmer
  106051. volker
  106052. calixarenes
  106053. supramolecular
  106054. mckervey
  106055. synthetic
  106056. approaches
  106057. large
  106058. diamondoid
  106059. hydroc
  106060. mckillop
  106061. mckillop
  106062. young
  106063. organic
  106064. synthesis
  106065. using
  106066. supported
  106067. reage
  106068. mckinney
  106069. mckinney
  106070. haworth
  106071. sigma
  106072. bonded
  106073. cyclopolyenyl
  106074. metal
  106075. mckinnon
  106076. mckinnon
  106077. investigations
  106078. bridged
  106079. potentially
  106080. mclafferty
  106081. mclafferty
  106082. tandem
  106083. spectrometry
  106084. ms/ms
  106085. promising
  106086. mclafferty
  106087. michnowicz
  106088. state
  106089. gc/ms
  106090. mclafferty
  106091. turecek
  106092. frantisek
  106093. interpretation
  106094. mclnnes
  106095. mcmullen
  106096. mcmurry
  106097. mcmurry
  106098. lectka
  106099. thomas
  106100. three
  106101. center
  106102. electron
  106103. mcnab
  106104. mcnab
  106105. meldrum's
  106106. dimethyl
  106107. dioxane
  106108. dione
  106109. mcnab
  106110. thornley
  106111. pyrrolizin
  106112. heterocycles
  106113. mcnally
  106114. mcnamara
  106115. mcneil
  106116. mcneil
  106117. darvill
  106118. albersheim
  106119. structural
  106120. polymers
  106121. mcomie
  106122. mcomie
  106123. recent
  106124. developments
  106125. protecting
  106126. groups
  106127. mcpba
  106128. mcquillin
  106129. mcquillin
  106130. parker
  106131. stephenson
  106132. transition
  106133. metal
  106134. mcvey
  106135. me2cu
  106136. me3si
  106137. me3sicbr3
  106138. me3sisnbu3
  106139. meador
  106140. meaning
  106141. means
  106142. rements
  106143. mecha
  106144. mechamisms
  106145. mechanical
  106146. mechanically
  106147. mechanics
  106148. mechanics-based
  106149. mechanism
  106150. mechanism
  106151. mechanism
  106152. catalysis
  106153. nucleophilic
  106154. substitution
  106155. mechanism
  106156. stereochemistry
  106157. zirconium
  106158. catalyzed
  106159. mechanism
  106160. study
  106161. woiff
  106162. rearrangement
  106163. mechanism
  106164. alkene
  106165. epoxidation
  106166. chromium
  106167. mangane
  106168. mechanism
  106169. asymmetric
  106170. epoxidation
  106171. using
  106172. sharpless
  106173. mechanism
  106174. cytochrome
  106175. p-450
  106176. catalyzed
  106177. tions
  106178. mechanism
  106179. grignard
  106180. reagent
  106181. formation
  106182. surface
  106183. nature
  106184. mechanism
  106185. homogeneous
  106186. hydrogenation
  106187. mechanism
  106188. lithium
  106189. cuprate
  106190. conjugate
  106191. addition
  106192. neutral
  106193. mechanism
  106194. oxidation
  106195. tungsten
  106196. dihydrofur
  106197. mechanism
  106198. oxygen
  106199. nitrogen
  106200. transfer
  106201. mechanism
  106202. ozonolysis
  106203. mechanism
  106204. quinone
  106205. methide
  106206. initiated
  106207. cyclization
  106208. reactio
  106209. mechanism
  106210. sigmatropic
  106211. shift
  106212. vinylcyclobutanol
  106213. mechanism
  106214. diimine
  106215. copper-catalyzed
  106216. asymmetric
  106217. aziridi
  106218. mechanism
  106219. enantioselective
  106220. dihydroxylation
  106221. olefins
  106222. mechanism
  106223. enantioselective
  106224. dihyroxylation
  106225. olefins
  106226. mechanism
  106227. reaction
  106228. between
  106229. singlet
  106230. oxygen
  106231. mechanism
  106232. grignard
  106233. reaction
  106234. mechanism
  106235. hydrogenolysis
  106236. thiophene
  106237. bimetallic
  106238. mechanism
  106239. lewis
  106240. cat6alyzed
  106241. reaction
  106242. mechanism
  106243. proline-catalysed
  106244. enantioselective
  106245. aldol
  106246. mechanism
  106247. reaction
  106248. atomic
  106249. carbon
  106250. pyrrole
  106251. mechanism
  106252. thermal
  106253. photochemical
  106254. decomposition
  106255. mechanism-based
  106256. mechanism-based
  106257. dual-action
  106258. cephalosporins
  106259. mechanismsq
  106260. mechanisms
  106261. catalysis
  106262. electron
  106263. transfer
  106264. chemistry
  106265. mechanisms
  106266. rates
  106267. electrophilic
  106268. substitution
  106269. reactions
  106270. mechanisms
  106271. reactivity
  106272. electron-transfer-in
  106273. aroma
  106274. mechanisms
  106275. stereochemistry
  106276. alkali
  106277. metal
  106278. reductions
  106279. mechanisms
  106280. stereochemistry
  106281. heterolytic
  106282. fragmentations
  106283. mechanisms
  106284. stereo-differentiati
  106285. metal-catalyzed
  106286. reactions
  106287. mechanisms
  106288. aromatic
  106289. nucleophilic
  106290. stitution
  106291. reactions
  106292. mechanisms
  106293. elimination
  106294. reactions
  106295. catalysed
  106296. bases
  106297. mechanisms
  106298. group
  106299. transfer
  106300. anionic
  106301. transition
  106302. metal
  106303. mechanisms
  106304. heterogeneous
  106305. catalysis
  106306. mechanisms
  106307. hydrolysis
  106308. thioacetals
  106309. mechanisms
  106310. inorganic
  106311. organometallic
  106312. reactions
  106313. mechanisms
  106314. intramolecular
  106315. activation
  106316. carbon-hydrogen
  106317. mechanisms
  106318. molecular
  106319. recognition
  106320. investigation
  106321. organic
  106322. mechanisms
  106323. oxidative
  106324. addition
  106325. organic
  106326. halides
  106327. group
  106328. mechanisms
  106329. pericyclic
  106330. reactions
  106331. quantitative
  106332. mechanisms
  106333. reactions
  106334. emphasis
  106335. organotin
  106336. compounds
  106337. mechanisms
  106338. solvolytic
  106339. alkene
  106340. forming
  106341. elimination
  106342. reaction
  106343. mechanisms
  106344. stereochemistry
  106345. alkali
  106346. metal
  106347. reductions
  106348. mechanisms
  106349. solvolytic
  106350. alkene-forming
  106351. elimination-reaction@
  106352. mechanistic
  106353. ingenuity
  106354. enzyme
  106355. catalysis
  106356. dehydroquinate
  106357. mechanisticand@
  106358. mediated
  106359. medium
  106360. nitrogen
  106361. heterocycles@
  106362. meijere
  106363. membered
  106364. menger
  106365. fredric
  106366. enzyme
  106367. reactivity
  106368. organic
  106369. perspecti@
  106370. ionic
  106371. heterocycles@
  106372. meso-compounds@
  106373. metal
  106374. metal
  106375. ammonia
  106376. reduction
  106377. aromatic
  106378. compounds@
  106379. etal-organic
  106380. approach
  106381. stereoselective
  106382. synthesis
  106383. exocy@
  106384. metallacyclobutane
  106385. complexes
  106386. group-8
  106387. transition-metal@
  106388. metallo-organic
  106389. chemistry@
  106390. metals
  106391. tarnowski
  106392. thiocoumarins
  106393. advances
  106394. method
  106395. methodology
  106396. establish
  106397. 13-difunctionality
  106398. methods
  106399. methods
  106400. oxidation
  106401. organic
  106402. compounds
  106403. alkanes
  106404. alken
  106405. methoxyacrylic
  106406. mechanisms
  106407. solvolytic
  106408. alkene-forming
  106409. elimination-reaction
  106410. mechanistic
  106411. mechanistic
  106412. preparative
  106413. aspects
  106414. vinyl
  106415. cation
  106416. chemistr
  106417. mechanistic
  106418. synthetic
  106419. aspects
  106420. amine-enone
  106421. single
  106422. mechanistic
  106423. aspects
  106424. associated
  106425. cyclization
  106426. mechanistic
  106427. aspects
  106428. diels
  106429. alder
  106430. reactions
  106431. creitical
  106432. mechanistic
  106433. aspects
  106434. transition
  106435. metal
  106436. catal
  106437. alcohol
  106438. mechanistic
  106439. evidence
  106440. ortho
  106441. directed
  106442. lithiation
  106443. mechanistic
  106444. ingenuity
  106445. enzyme
  106446. catalysis
  106447. dehydroquinate
  106448. mechanistic
  106449. investigations
  106450. biomimetic
  106451. polycyclization
  106452. mechanistic
  106453. studies
  106454. catalyzed
  106455. asymmetric
  106456. diels-alde
  106457. mechanistic
  106458. studies
  106459. pummerer
  106460. reaction
  106461. acyclic
  106462. sulfoxid
  106463. mechanistically
  106464. echnnism
  106465. mechnnistic
  106466. mechoulam
  106467. media
  106468. mediat
  106469. mediate
  106470. mediatedC
  106471. mediated
  106472. mediation
  106473. mediation
  106474. reactivity
  106475. strong
  106476. lewis
  106477. ticl4
  106478. mediators
  106479. medical
  106480. medical
  106481. biochemical
  106482. chemical
  106483. aspect
  106484. radicals
  106485. medich
  106486. medicinaln
  106487. medicine
  106488. medicines
  106489. medina
  106490. medio
  106491. medio-and
  106492. medium
  106493. medium
  106494. dependent
  106495. trapping
  106496. diazoalkane
  106497. intermediates
  106498. durin
  106499. medium
  106500. nitrogen
  106501. heterocycles
  106502. medium
  106503. sized
  106504. rings
  106505. expansion
  106506. medium-ring
  106507. medium-sized
  106508. meeder
  106509. meerwein
  106510. meerwein-ponndorf-ve
  106511. meerwein-ponndorf-ve
  106512. reductions
  106513. oppenauer
  106514. oxidations
  106515. meeting
  106516. meets
  106517. mehmet
  106518. mehra
  106519. mehrotra
  106520. mehrotra
  106521. singh
  106522. sogani
  106523. hetero
  106524. metallic
  106525. alkal
  106526. mehrotra
  106527. singh
  106528. sogani
  106529. recent
  106530. advances
  106531. chemist
  106532. mehrotra
  106533. singh
  106534. anirudh
  106535. organometallic
  106536. chemistry
  106537. unifie
  106538. meidine
  106539. meienhofer
  106540. meienhofer
  106541. azide
  106542. method
  106543. peptide
  106544. synthesis
  106545. pepti
  106546. meienhofer
  106547. mixed
  106548. carbonic
  106549. anhydride
  106550. method
  106551. peptide
  106552. meier
  106553. meier
  106554. herbert
  106555. cyclic
  106556. alkynes
  106557. enynes
  106558. dienynes
  106559. synthetic
  106560. meijer
  106561. meijere
  106562. meijere
  106563. meinel
  106564. meinwald
  106565. meisenheimer
  106566. meister
  106567. meixiang
  106568. mekelburger
  106569. mekelburger
  106570. bernhard
  106571. jaworek
  106572. wilfried
  106573. vogtle
  106574. fritz
  106575. mel'nikov
  106576. mel'nikov
  106577. photochemical
  106578. reactions
  106579. ralic
  106580. melanins
  106581. meldola
  106582. meldola
  106583. lecture
  106584. aromatic
  106585. interactions
  106586. molecul
  106587. meldrum's
  106588. meldrum's
  106589. organic
  106590. synthesis
  106591. meleard
  106592. melent'eva
  106593. meliaceae
  106594. melikyan
  106595. melikyan
  106596. gagik
  106597. manganese
  106598. mediated
  106599. reactions
  106600. unsatur
  106601. mella
  106602. meller
  106603. mellon
  106604. melloni
  106605. melloni
  106606. modena
  106607. tonellato
  106608. relative
  106609. reactivities
  106610. melnikov
  106611. melts
  106612. melvin
  106613. member
  106614. membered
  106615. membered
  106616. membered-ring
  106617. membrane
  106618. membranes
  106619. memmesheimer
  106620. memmesheimer
  106621. holger
  106622. regitz
  106623. manfred
  106624. phosphirenes
  106625. memmesheimer
  106626. holger
  106627. regitz
  106628. manfred
  106629. carbenes
  106630. memming
  106631. memming
  106632. rudiger
  106633. photoinduced
  106634. charge
  106635. transfer
  106636. processes
  106637. memorial
  106638. memory
  106639. menchikov
  106640. mendez
  106641. mendoza
  106642. menger
  106643. menger
  106644. groups
  106645. organic
  106646. molecules
  106647. operate
  106648. collecti
  106649. menger
  106650. structure
  106651. micelles
  106652. 197912
  106653. accounts
  106654. menger
  106655. fredric
  106656. enzyme
  106657. reactivity
  106658. organic
  106659. perspecti
  106660. menichetti
  106661. menlo
  106662. menon
  106663. menshutkin
  106664. menthone
  106665. mention
  106666. ments
  106667. mercapto
  106668. mercedes
  106669. merchan
  106670. mercier
  106671. mercuric
  106672. mercury
  106673. mercury
  106674. palladium
  106675. catalysed
  106676. sigmatropic
  106677. rearran
  106678. merenyi
  106679. merged
  106680. merkuhhev
  106681. meroionic
  106682. meroionic
  106683. heterocycles
  106684. review
  106685. merrifield
  106686. merrimack
  106687. merritt
  106688. merritt
  106689. clerodane
  106690. diterpenoids
  106691. 19929
  106692. mersh
  106693. mesher
  106694. mesitylborane
  106695. mesitylenesulfonylhy
  106696. meskens
  106697. meskens
  106698. methods
  106699. preparation
  106700. acetals
  106701. epoxides
  106702. asymmetric
  106703. synthesis
  106704. enantioselective
  106705. openi
  106706. ionic
  106707. heterocycles
  106708. ionic
  106709. heterocycles
  106710. review
  106711. meso-anhydrides
  106712. eso-epoxides
  106713. meso-epoxides
  106714. asymmetric
  106715. synthesis
  106716. enantioselective
  106717. openi
  106718. mesoionic
  106719. mesoionics
  106720. mesomeric
  106721. message
  106722. messenger
  106723. mestroni
  106724. mesylates
  106725. mesylation
  106726. mesyloxy
  106727. meszaros
  106728. metabolic
  106729. metabolically
  106730. metabolism
  106731. metabolism
  106732. heterocycles
  106733. metabolism
  106734. sulfur
  106735. containing
  106736. xenobiotics
  106737. metabolite
  106738. metabolites
  106739. metacyclophanes
  106740. metai
  106741. metalz
  106742. metal
  106743. metal
  106744. metal
  106745. aromatic
  106746. compounds
  106747. metal
  106748. carbonyl-promoted
  106749. carbon-sulfur
  106750. cleavage
  106751. reaction
  106752. metal
  106753. catalyzed
  106754. cyclopropene
  106755. rearrangements
  106756. benzannulati
  106757. metal
  106758. catalyzed
  106759. cyclopropene
  106760. rearrangements
  106761. benzoannulat
  106762. metal
  106763. catalyzed
  106764. direct
  106765. hydroxy
  106766. epoxidation
  106767. olefins
  106768. metal
  106769. catalyzed
  106770. intramolecular
  106771. reactions
  106772. diazo
  106773. ketones
  106774. metal
  106775. catalyzed
  106776. intramolecular
  106777. reactions
  106778. diazo
  106779. ketones
  106780. metal
  106781. catalyzed
  106782. organic
  106783. photoreactions
  106784. chemo
  106785. regioselect
  106786. metal
  106787. catalyzed
  106788. organic
  106789. photoreactions
  106790. photoreaction
  106791. metal
  106792. catalyzed
  106793. reaction
  106794. furans
  106795. ethers
  106796. metal
  106797. cluster
  106798. complexes
  106799. containing
  106800. heteroatom-substitut
  106801. metal
  106802. complexes
  106803. buckminsterfullerene
  106804. metal
  106805. complexes
  106806. small
  106807. cycloalkynes
  106808. arynes
  106809. metal
  106810. directed
  106811. stereoselective
  106812. functionalization
  106813. alkenes
  106814. metal
  106815. homoenolates
  106816. metal
  106817. homoenolates
  106818. siloxycyclopropanes
  106819. metal
  106820. hydride
  106821. mediated
  106822. intramolecular
  106823. pinacol
  106824. coupling
  106825. metal
  106826. promoted
  106827. reactions
  106828. organosulphur
  106829. compounds
  106830. metal
  106831. ligand
  106832. protective
  106833. group
  106834. tuning
  106835. means
  106836. contr
  106837. metal
  106838. mediated
  106839. additions
  106840. conjugated
  106841. dienes
  106842. metal
  106843. mediated
  106844. enantioselective
  106845. access
  106846. unfunctionalized
  106847. metal
  106848. versus
  106849. silyl
  106850. triflate
  106851. catalysis
  106852. mukaiyama
  106853. aldol
  106854. metal-acetylene
  106855. metal-activated
  106856. metal-activated
  106857. metal-acyl
  106858. metal-alkyl
  106859. metal-alkylidene
  106860. metal-ammonia
  106861. metal-ammonia
  106862. reduction
  106863. cyclic
  106864. aliphatic
  106865. ketones
  106866. metal-assisted
  106867. metal-carbene
  106868. metal-carbene
  106869. cycloadditions
  106870. metal-carbon
  106871. metal-catalysed
  106872. metal-catalysis
  106873. metal-catalyzed
  106874. metal-catalyzed
  106875. cycloaddition
  106876. small
  106877. compounds
  106878. metal-catalyzed
  106879. direct
  106880. hydroxy-epoxidation
  106881. olefins
  106882. metal-centered
  106883. metal-containing
  106884. metal-directed
  106885. metal-directed
  106886. stereoselective
  106887. functionalizations
  106888. alkenes
  106889. metal-halogen
  106890. metal-induced
  106891. metal-induced
  106892. rearrangements
  106893. nsertions
  106894. cyclopropyl
  106895. metal-ligand
  106896. metal-ligand
  106897. multiple
  106898. bonds
  106899. metal-mediated
  106900. metal-mediated
  106901. enantioselective
  106902. access
  106903. unfunctionalized
  106904. metal-metal
  106905. metal-organic
  106906. metal-organic
  106907. approach
  106908. stereoselective
  106909. synthesis
  106910. exocy
  106911. metal-promoted
  106912. metal-stabilized
  106913. metal-tin
  106914. metalated
  106915. metalated
  106916. 2-alkenyl
  106917. carbamates
  106918. chiral
  106919. homoenolate
  106920. reagents
  106921. metalation
  106922. metalation
  106923. alkylation
  106924. 36-dihydrothiazine-1
  106925. prepared
  106926. metalation
  106927. electrophilic
  106928. substitution
  106929. amine
  106930. derivativ
  106931. metalation
  106932. metal-assisted
  106933. formation
  106934. electron
  106935. metalation
  106936. arylmethyl
  106937. methyl
  106938. ethers
  106939. connection
  106940. metalation
  106941. indole
  106942. n-methylindole
  106943. n-phenylindole
  106944. metall
  106945. metall
  106946. macrocycles
  106947. supramolecular
  106948. chemistry
  106949. metalla
  106950. metallabenzene
  106951. metallabenzene
  106952. chemistry
  106953. metallacycles
  106954. metallacyclic
  106955. metallacyclobutane
  106956. metallacyclobutane
  106957. complexes
  106958. group-8
  106959. transition-metal
  106960. metallacyclobutanes
  106961. metallacyclobutanes
  106962. synthons
  106963. catalysts
  106964. metallacyclotetraaza
  106965. metalladienes
  106966. metallaoxetanes
  106967. metallaoxetanes
  106968. intermediate
  106969. oxygen-transfer
  106970. reactions
  106971. metallated
  106972. metallation
  106973. metallation
  106974. metal
  106975. assisted
  106976. formation
  106977. electron
  106978. metallation
  106979. metal
  106980. halogen
  106981. exchange
  106982. reactions
  106983. imidazol
  106984. metallation
  106985. metal-assisted
  106986. formation
  106987. electron
  106988. metallation
  106989. metal-halogen
  106990. exchange
  106991. reactions
  106992. imidazol
  106993. metallations
  106994. metallations
  106995. organolithium
  106996. compounds
  106997. metallic
  106998. metallics
  106999. metallo
  107000. metallo-dipole
  107001. metallo-ene
  107002. metallo-ene
  107003. reactions
  107004. metallo-imines
  107005. metallo-imines
  107006. reagents
  107007. organic
  107008. synthesis
  107009. metallo-organic
  107010. metallo-organic
  107011. chemistry
  107012. metallo-porphyrins
  107013. metalloboranes
  107014. metallocarboranes
  107015. metallocarboxylates
  107016. metallocatalysts
  107017. metallocene
  107018. metallocene
  107019. carbene
  107020. complexes
  107021. related
  107022. compounds
  107023. titan
  107024. metallocenes
  107025. metallocenes
  107026. reaction
  107027. intermediates
  107028. metallocupration
  107029. metallodiporphyrin
  107030. metalloenamines
  107031. metalloenzymes
  107032. metalloids
  107033. metalloles
  107034. metallomacrocycles
  107035. metallomacrocycles
  107036. novel
  107037. amphoteric
  107038. macrocycles
  107039. metal
  107040. metallomacrocycles
  107041. supramolecular
  107042. chemistry
  107043. metalloporphinoids
  107044. metalloporphyrin
  107045. metalloporphyrin-med
  107046. metalloporphyrins
  107047. metalloporphyrins
  107048. versatile
  107049. catalysts
  107050. oxidation
  107051. react
  107052. metallosupramolecula
  107053. metallotropic
  107054. metalloxirane
  107055. metalocupration
  107056. metals
  107057. metals
  107058. metamorphosis
  107059. metamorphosis
  107060. synthetic
  107061. strategies
  107062. allylic
  107063. silanes
  107064. metanomski
  107065. metanomski
  107066. compendium
  107067. macromolecular
  107068. nomenclature
  107069. metaphosphates
  107070. metastable
  107071. metastases
  107072. metathasis
  107073. metathesis
  107074. metathesis/isomeriza
  107075. meter
  107076. meterorites
  107077. metgner
  107078. tarnowski
  107079. thiocoumarins
  107080. advances
  107081. synthesis
  107082. pyridines
  107083. quinolines
  107084. methacryloylsultams
  107085. methallyl
  107086. methane
  107087. methanelike
  107088. methanesulfenyl
  107089. methanesulfenyl
  107090. triflate
  107091. promoted
  107092. imino
  107093. sulfenylation
  107094. methanesulfonates
  107095. methanetetraboronic
  107096. methanetriboronic
  107097. methanetricarboxylic
  107098. methanide
  107099. methano
  107100. methanoamino|
  107101. methanoanthracenes
  107102. methanofullerenes
  107103. methanolS
  107104. methanolsE
  107105. methanomaino
  107106. methide
  107107. methides
  107108. methiodides
  107109. methionine
  107110. method}
  107111. method
  107112. methoden
  107113. methodolo
  107114. methodolo
  107115. synthesis
  107116. heterocyclic
  107117. compounds
  107118. methodologies
  107119. methodology
  107120. methodology
  107121. stereochemical
  107122. control
  107123. bioactive
  107124. natural
  107125. methodology
  107126. efficient
  107127. synthesis
  107128. 34-differentially
  107129. methodology
  107130. formation
  107131. quaternary
  107132. centres
  107133. methodology
  107134. establish
  107135. 13-difunctionality
  107136. methods
  107137. methods
  107138. methods
  107139. possibilities
  107140. nucleophilic
  107141. acylation
  107142. methods
  107143. angular
  107144. alkoxycarbonylation
  107145. fused
  107146. rings
  107147. methods
  107148. increasing
  107149. efficiency
  107150. catalysis
  107151. methods
  107152. construction
  107153. indolizine
  107154. nucleus
  107155. methods
  107156. oxidation
  107157. organic
  107158. compounds
  107159. alcohols
  107160. methods
  107161. oxidation
  107162. organic
  107163. compounds
  107164. alkanes
  107165. alken
  107166. methods
  107167. oxidation
  107168. organic
  107169. compounds
  107170. alkanes
  107171. alken
  107172. methods
  107173. preparation
  107174. acetals
  107175. alcohols
  107176. methods
  107177. preparation
  107178. bridgehead
  107179. olefins
  107180. methods
  107181. synthesis
  107182. 3-oxocyclopentenes
  107183. methods
  107184. synthesis
  107185. allylsilanes
  107186. methods
  107187. synthesis
  107188. allylsilanes
  107189. parts
  107190. methods
  107191. synthesis
  107192. alpha-keto
  107193. esters
  107194. methods
  107195. synthesis
  107196. antiinflammatory
  107197. 2-arylpropioni
  107198. methods
  107199. synthesis
  107200. cycloproparenes
  107201. methods
  107202. asymmetric
  107203. synthesis
  107204. enantioselective
  107205. catalytic
  107206. methods
  107207. reactivity
  107208. umpolung
  107209. methods
  107210. replacing
  107211. halogen
  107212. aromatic
  107213. compounds
  107214. rs-fun
  107215. methods
  107216. synthesis
  107217. acrolein
  107218. substituted
  107219. deriv
  107220. methods
  107221. synthesis
  107222. acrolein
  107223. o-substituted
  107224. deriv
  107225. methods
  107226. synthesis
  107227. dithiocarboxylic
  107228. acids
  107229. esters
  107230. methoxy
  107231. methoxyacrylic
  107232. methoxyacrylic
  107233. methoxyallene
  107234. methoxyamines
  107235. methoxybenzyl
  107236. methoxycarbonyl
  107237. methoxycarbonylbicyc
  107238. methoxycarbonylethyn
  107239. methoxycarbonylnitro
  107240. methoxycephalosporin
  107241. methoxyethoxoyalumin
  107242. methoxyindole
  107243. methoxyindoles
  107244. methoxymethyl
  107245. methoxyphenyl
  107246. methoxyphenylhydrazo
  107247. methoxypyridinium
  107248. methuen
  107249. methyl
  107250. methyl
  107251. 2-benzoylamino-3-dim
  107252. synthesis
  107253. heterocyclic
  107254. methyl
  107255. trifluoromethyl
  107256. pyrrole
  107257. carboxylates
  107258. methyl
  107259. isothioc
  107260. anate
  107261. natural
  107262. product
  107263. commercial
  107264. methyl/phenyl
  107265. methyl/phenyl
  107266. exchange
  107267. between
  107268. palladium
  107269. phosphine
  107270. methylalkylamines
  107271. methylalumination
  107272. hylamides
  107273. methylammonium
  107274. methylanecyclopropan
  107275. methylated
  107276. methylation
  107277. methylbenzimidazoles
  107278. methylbenzofuran
  107279. methylbiladienes
  107280. methylbutylphosphine
  107281. methylcarbapenem
  107282. methylcarbapenems
  107283. methylcarbene
  107284. methylcoumarin
  107285. methylcyclohex
  107286. methylenation
  107287. methylene
  107288. methylene
  107289. nonfunctionalized
  107290. alkylidene
  107291. transfer
  107292. methylene-13
  107293. methyleneamino
  107294. methyleneboranes
  107295. methylenecarbene
  107296. methylenecyclobutane
  107297. methylenecyclohexane
  107298. methyl
  107299. isothioc
  107300. anate
  107301. natural
  107302. product
  107303. commercial
  107304. methylaluminum@
  107305. methylenecyclohexane
  107306. methynolide
  107307. prelog-djerasi
  107308. lactonic
  107309. exercise@
  107310. meyers
  107311. asymmetric
  107312. carbon
  107313. carbon
  107314. formation
  107315. chir@
  107316. michael
  107317. michele@
  107318. midland@
  107319. mikhaleva
  107320. miller
  107321. audrey
  107322. writing
  107323. reaction
  107324. mechanisms
  107325. organic
  107326. chemist@
  107327. minkin
  107328. dipole
  107329. moments
  107330. stereochemistry
  107331. organic
  107332. mislow
  107333. mismatched@
  107334. mitsunobu@
  107335. mixture@
  107336. model
  107337. studies
  107338. stereoelectronic
  107339. effect
  107340. mediat@
  107341. models
  107342. modern
  107343. methods
  107344. prepare
  107345. monofluoroaliphatic
  107346. compounds
  107347. will@
  107348. moggi
  107349. juris
  107350. sandrini
  107351. manfrin
  107352. photocatalysis
  107353. molecular
  107354. molecular
  107355. recognition
  107356. immunophilins
  107357. immunophilin-liga@
  107358. molecules
  107359. molecules
  107360. large
  107361. cavities
  107362. supramolecular
  107363. chemistry@
  107364. monique@
  107365. okhlobystin
  107366. inorganic
  107367. radical
  107368. methylenecyclohexane
  107369. methylenecyclopentan
  107370. methylenecyclopenten
  107371. methylenecyclopropan
  107372. methylenecyclopropyl
  107373. methylenelactones
  107374. methyleneoxolanes
  107375. methylenephosphanes
  107376. methylenetributylpho
  107377. methyleniminium
  107378. methylenomycin
  107379. methylformamido
  107380. methylfucosamine
  107381. methylfuran
  107382. methylfurans
  107383. methylide
  107384. methylimidazo
  107385. methylimino
  107386. methylindol
  107387. methylindole
  107388. methyllithium
  107389. methylmetallics
  107390. methylnogarol
  107391. methyloxazoles
  107392. methyloxindole
  107393. methylphenyl
  107394. methylpyrazoles
  107395. methylpyrazolo
  107396. methylpyridine
  107397. methylraumacline
  107398. methylstannanes
  107399. methyltetracyclo
  107400. methylthiirane
  107401. methylthio
  107402. methylthiobutenolide
  107403. methylthiomethyltrim
  107404. methylthiotrimethyls
  107405. methyne
  107406. methynolide
  107407. methynolide
  107408. prelog-djerasi
  107409. lactonic
  107410. exercise
  107411. metin
  107412. metiu
  107413. metiu
  107414. whitesides
  107415. basis
  107416. orbital
  107417. symmetry
  107418. metric
  107419. metwally
  107420. metyl
  107421. metzger
  107422. metzger
  107423. thiazole
  107424. derivatives
  107425. chemistry
  107426. hetero
  107427. metzger
  107428. ladder
  107429. sequencing
  107430. peptides
  107431. proteins
  107432. metzger
  107433. largeau
  107434. casadevall
  107435. lipids
  107436. macromolecular
  107437. metzner
  107438. metzner
  107439. patrick
  107440. thiocarbonyl
  107441. compounds
  107442. carbon
  107443. meunier
  107444. meunier
  107445. bernard
  107446. metalloporphyrins
  107447. versatile
  107448. catalysts
  107449. meunier
  107450. bernard
  107451. potassium
  107452. monopersulfate
  107453. another
  107454. primar
  107455. meuret
  107456. meutter
  107457. mevinic
  107458. mevinoid
  107459. mevinolin
  107460. mewes
  107461. meyer
  107462. meyer
  107463. marion
  107464. o'hagan
  107465. david
  107466. fluorinated
  107467. natural
  107468. products
  107469. meyer-schuster
  107470. meyers
  107471. meyers
  107472. asymmetric
  107473. carbon
  107474. carbon
  107475. formation
  107476. meyerstein
  107477. mezey
  107478. mezey
  107479. shape
  107480. chemistry
  107481. introduction
  107482. molecular
  107483. mezheritskii
  107484. mezheritskii
  107485. wasserman
  107486. dorofeenko
  107487. reactions
  107488. mezhetritskii
  107489. mgbr/br
  107490. mical
  107491. micellar
  107492. micelles
  107493. michael
  107494. michael
  107495. michael
  107496. addition
  107497. imines
  107498. alkynylcarbene
  107499. complexes
  107500. michael
  107501. addition
  107502. organolithium
  107503. compounds
  107504. review
  107505. michael
  107506. addition
  107507. reactions
  107508. highly
  107509. functionalized
  107510. michael
  107511. additions
  107512. functionalized
  107513. organozinc
  107514. reagents
  107515. michael
  107516. indolizidine
  107517. quinolizidine
  107518. alkaloids
  107519. natural
  107520. michael
  107521. quinoline
  107522. quinazoline
  107523. acridone
  107524. alkaloids
  107525. michael
  107526. quinoline
  107527. quinazoline
  107528. acridone
  107529. alkaloids
  107530. michael
  107531. joseph
  107532. pattenden
  107533. gerald
  107534. marine
  107535. metabolites
  107536. michael
  107537. addition
  107538. phthalimide
  107539. salts
  107540. chiral
  107541. michaelis
  107542. michal
  107543. michale
  107544. michalska
  107545. michalski
  107546. michalski
  107547. reimschussel
  107548. kaminski
  107549. organic
  107550. monothiopyroph
  107551. michel
  107552. michele
  107553. micheli
  107554. micheline
  107555. michinori
  107556. michio
  107557. michiya
  107558. michl
  107559. michl
  107560. excited
  107561. states
  107562. oxocarbon
  107563. dianions
  107564. oxocarbo
  107565. michno
  107566. michnowicz
  107567. mickel
  107568. micro
  107569. micro-hplc
  107570. microalga
  107571. microbial
  107572. microbial
  107573. oxidation
  107574. aromatics
  107575. enantiocontrolled
  107576. synthe
  107577. microbial
  107578. oxidation
  107579. organic
  107580. sulfur
  107581. compounds
  107582. microbial
  107583. pyran-2-ones
  107584. dihydropyran-2-ones
  107585. microbiological
  107586. microheterogeneous
  107587. microorganisms
  107588. microporous
  107589. microscale
  107590. microsensors
  107591. microsequence
  107592. microstructures
  107593. microwave
  107594. middlemissn
  107595. middlemiss
  107596. watson
  107597. medicinal
  107598. chemistry
  107599. study
  107600. middleton
  107601. midland
  107602. midland
  107603. asymmetric
  107604. synthesis
  107605. boranes
  107606. chiral
  107607. allenic
  107608. midura
  107609. mieczyslaw
  107610. mielniczak
  107611. miethchen
  107612. migrating
  107613. migration
  107614. migrations
  107615. migratory
  107616. migratory-insertion
  107617. migratory-insertion
  107618. carbon
  107619. monoxide
  107620. metal-acyl
  107621. bonds
  107622. miguel
  107623. mihara
  107624. mihelic
  107625. mihelich
  107626. mihir
  107627. mikael
  107628. mikami
  107629. mikami
  107630. koichi
  107631. nakai
  107632. takeshi
  107633. acyclic
  107634. stereocontrol
  107635. mikami
  107636. koichi
  107637. shimizu
  107638. masaki
  107639. asymmetric
  107640. reactions
  107641. mikami
  107642. koichi
  107643. shimizu
  107644. masaki
  107645. stereoelectronic
  107646. rules
  107647. addit
  107648. mikami
  107649. koichi
  107650. terada
  107651. masahiro
  107652. narisawa
  107653. satoshi
  107654. nakai
  107655. takeshi
  107656. mikanecic
  107657. mikaya
  107658. mikaya
  107659. varlamov
  107660. zaikin
  107661. prostakov
  107662. spectr
  107663. mikhail
  107664. mikhailov
  107665. mikhaleva
  107666. mikhaleva
  107667. mikiji
  107668. miklos
  107669. mikolajczyk
  107670. mikoyajczyk
  107671. mikoyajczyk
  107672. kieybasinski
  107673. recent
  107674. developments
  107675. mil'vitskaya
  107676. milaeva
  107677. milan
  107678. milbemycin
  107679. milbemycins
  107680. rapid
  107681. azide
  107682. mediated
  107683. palladium
  107684. catalyzed
  107685. cleavage
  107686. selective
  107687. oxygenation
  107688. sulfides
  107689. sulfoxides
  107690. induced
  107691. defluorination
  107692. butatrienes
  107693. stereoselect
  107694. mileshkevich
  107695. mileshkevich
  107696. novikova
  107697. relations
  107698. milewska
  107699. milgrom
  107700. milgrom
  107701. vitamin
  107702. summit
  107703. milind
  107704. millar
  107705. millauer
  107706. miller
  107707. miller
  107708. audrey
  107709. writing
  107710. reaction
  107711. mechanisms
  107712. organic
  107713. chemist
  107714. milligrams
  107715. mills
  107716. milman
  107717. milos
  107718. milstem
  107719. milton
  107720. mimetic
  107721. mimetics
  107722. mimic
  107723. mimicking
  107724. mimicry
  107725. mimics
  107726. mimoun
  107727. minachev
  107728. minachev
  107729. dergachev
  107730. aromatization
  107731. molecular
  107732. minale
  107733. minami
  107734. minami
  107735. motoyoshiya
  107736. vinylphosphonates
  107737. organic
  107738. minami
  107739. yamamoto
  107740. chemistry
  107741. phosphonium
  107742. salts
  107743. minamikawa
  107744. minayaev
  107745. mingos
  107746. mingos
  107747. michael
  107748. baghurst
  107749. david
  107750. applications
  107751. microwav
  107752. miniature
  107753. minimum
  107754. minisci
  107755. minisci
  107756. citterio
  107757. polar
  107758. effects
  107759. radical
  107760. reactions
  107761. minkinO
  107762. minkin
  107763. dipole
  107764. moments
  107765. stereochemistry
  107766. organic
  107767. minkin
  107768. glukhovtsev
  107769. simkin
  107770. aromaticity
  107771. minkin
  107772. olekhnovich
  107773. zhdanov
  107774. molecular
  107775. design
  107776. minkin
  107777. simkin
  107778. minayaev
  107779. quantum
  107780. chemistry
  107781. minor
  107782. minor
  107783. synthetic
  107784. capacities
  107785. bakers
  107786. yeast
  107787. towards
  107788. unnatural
  107789. minorgroove
  107790. minoru
  107791. minsky
  107792. mintz
  107793. minuti
  107794. minyaev
  107795. miotti
  107796. miquel
  107797. miracle
  107798. miranda
  107799. miranda
  107800. miguel
  107801. garcia
  107802. hermenegildo
  107803. triphenylpyrylium
  107804. mirbach
  107805. mirco
  107806. miroestrol
  107807. mironov
  107808. mironov
  107809. fedotov
  107810. evert
  107811. adamantane
  107812. structu
  107813. mironov
  107814. sheludyakov
  107815. kozyukov
  107816. phosgene
  107817. mironova
  107818. miroslaw
  107819. mirskova
  107820. mirzaei
  107821. miscellaneous
  107822. mishin
  107823. misiti
  107824. mislow
  107825. mislow
  107826. mislow-evans
  107827. misono
  107828. missed
  107829. mistry
  107830. mistures
  107831. misumi
  107832. misumi
  107833. otsubo
  107834. chemistry
  107835. multilayered
  107836. cyclophanes
  107837. misumi
  107838. soichi
  107839. recognitory
  107840. coloration
  107841. cations
  107842. chromoc
  107843. mitch
  107844. mitchellT
  107845. mitchell
  107846. understanding
  107847. benzannulenes
  107848. israel
  107849. mitchell
  107850. nickson
  107851. metabolism
  107852. sulfur
  107853. containing
  107854. mitchell
  107855. nickson
  107856. waring
  107857. biological
  107858. activity
  107859. mitin
  107860. mitomycin
  107861. mitomycins
  107862. mitosene
  107863. mitov
  107864. mitov
  107865. faucon
  107866. meleard
  107867. borothel
  107868. thermal
  107869. fluctuatio
  107870. mitoxantrone
  107871. mitra
  107872. mitra
  107873. kulkarni
  107874. shirwaikar
  107875. jagtap
  107876. cycloadditi
  107877. mitscher
  107878. mitsudo
  107879. mitsuhashi
  107880. mitsuhiko
  107881. mitsunobu
  107882. mitsunobu
  107883. processes
  107884. novel
  107885. triphenylphosphine
  107886. mitsunobu
  107887. diethyl
  107888. azodicarboxylate
  107889. tripheny
  107890. mitsunobu
  107891. reactions
  107892. glycals
  107893. phenoxide
  107894. nucleophiles
  107895. mitsuo
  107896. mitsuru
  107897. miura
  107898. miwako
  107899. mixed
  107900. mixtures
  107901. miyake
  107902. miyakoshi
  107903. miyashi
  107904. miyashita
  107905. miyata
  107906. miyata
  107907. naito
  107908. ninomiya
  107909. stereospecific
  107910. addition
  107911. miyazaki
  107912. miyazawa
  107913. miyoshi
  107914. mizhiritskii
  107915. mizumo
  107916. mizumo
  107917. ikeda
  107918. tsuchida
  107919. aromatic
  107920. amine
  107921. oxides
  107922. mizuno
  107923. mizuno
  107924. kazuhiko
  107925. otsuji
  107926. yoshio
  107927. addition
  107928. cycloaddition
  107929. mkrtchyan
  107930. ml236a
  107931. mlcoch
  107932. mmetry
  107933. based
  107934. oxidative
  107935. radical
  107936. cyclization
  107937. unsaturat
  107938. mn-catalyzed
  107939. mndzhoyan
  107940. ecular
  107941. topology
  107942. chemical
  107943. reactivity
  107944. polynuclear
  107945. ecular
  107946. tweezers
  107947. synthetic
  107948. receptors
  107949. sandwich
  107950. complexa
  107951. mobile
  107952. mobilities
  107953. mobility
  107954. mobius
  107955. mochalin
  107956. mochel
  107957. modak
  107958. model
  107959. studies
  107960. stereoelectronic
  107961. effect
  107962. mediat
  107963. modeling
  107964. modelling
  107965. models
  107966. models
  107967. models
  107968. peptide
  107969. receptors
  107970. modena
  107971. moderately
  107972. moderhack
  107973. moderhack
  107974. dietrich
  107975. imino
  107976. functionalized
  107977. oxazetidi
  107978. modern
  107979. modern
  107980. approaches
  107981. preparation
  107982. palladium
  107983. charcoa
  107984. modern
  107985. enolate
  107986. chemistry
  107987. regio
  107988. stereoselective
  107989. formation
  107990. modern
  107991. methods
  107992. introduction
  107993. fluorine
  107994. organic
  107995. modern
  107996. methods
  107997. monofluorination
  107998. aliphatic
  107999. organic
  108000. modern
  108001. methods
  108002. radical
  108003. deoxygemation
  108004. alcohols
  108005. modern
  108006. methods
  108007. radical
  108008. deoxygenation
  108009. alcohols
  108010. modern
  108011. methods
  108012. aryl-aryl
  108013. formation
  108014. modern
  108015. methods
  108016. prepare
  108017. monofluoroaliphatic
  108018. compounds
  108019. modern
  108020. methods
  108021. prepare
  108022. monofluoroaliphatic
  108023. compounds
  108024. modern
  108025. molecular
  108026. photochemistry
  108027. modern
  108028. spectroscopy
  108029. organolithium
  108030. compounds
  108031. modern
  108032. organoselenium
  108033. chemistry
  108034. modern
  108035. pulse
  108036. methods
  108037. resolution
  108038. spectroscopy
  108039. modern
  108040. separation
  108041. methods
  108042. modern
  108043. synthetic
  108044. design
  108045. symmetry
  108046. simplicity
  108047. efficiency
  108048. modern
  108049. thin-layer
  108050. chromatography
  108051. modes
  108052. modifcations
  108053. modification
  108054. modifications
  108055. modified
  108056. modified
  108057. raney
  108058. nickel
  108059. catalyst
  108060. heterogeneous
  108061. enantiodifferen
  108062. modifying
  108063. modular
  108064. modulation
  108065. modulators
  108066. moeller
  108067. moffatt
  108068. moggi
  108069. moggi
  108070. juris
  108071. sandrini
  108072. manfrin
  108073. photocatalysis
  108074. mogilevich
  108075. mogilevich
  108076. oxidative
  108077. polymerization
  108078. vinyl
  108079. monomers
  108080. mohamed
  108081. mohammad
  108082. mohammed
  108083. mohareb
  108084. mohiuddin
  108085. moieties
  108086. moiety
  108087. moiseenkov
  108088. moiseenkov
  108089. dragan
  108090. veselovskii
  108091. synthetic
  108092. applicat
  108093. moiseev
  108094. mokrushin
  108095. molander
  108096. molander
  108097. application
  108098. lanthanide
  108099. reagents
  108100. organi
  108101. molarities
  108102. molchanov
  108103. molding
  108104. molding
  108105. clays
  108106. efficient
  108107. catalysts
  108108. moldowan
  108109. molec
  108110. molecular
  108111. molecular
  108112. molecular
  108113. molecular
  108114. basis
  108115. catalytic
  108116. reactions
  108117. involving
  108118. trihapto-al
  108119. molecular
  108120. design
  108121. biological
  108122. action
  108123. enediynes
  108124. molecular
  108125. design
  108126. syntheses
  108127. biologically
  108128. active
  108129. compoun
  108130. molecular
  108131. design
  108132. chemical
  108133. synthesis
  108134. biological
  108135. action
  108136. molecular
  108137. mechanical
  108138. studies
  108139. olefin
  108140. metathesis
  108141. reacti
  108142. molecular
  108143. mechanics
  108144. organic
  108145. synthesis
  108146. molecular
  108147. rearrangements
  108148. lithium
  108149. aluminium
  108150. hydride
  108151. reduct
  108152. molecular
  108153. rearrangements
  108154. occurring
  108155. products
  108156. intramol
  108157. molecular
  108158. rearrangements
  108159. membrane
  108160. heteromonocyc
  108161. molecular
  108162. rearrangements
  108163. organosilicon
  108164. compounds
  108165. molecular
  108166. recognition
  108167. biophysical
  108168. organic
  108169. chemistry
  108170. molecular
  108171. recognition
  108172. metal
  108173. template
  108174. synthesis
  108175. molecular
  108176. recognition
  108177. immunophilins
  108178. immunophilin-liga
  108179. molecular
  108180. recognition
  108181. model
  108182. systems
  108183. molecular
  108184. self-assembly
  108185. nanochemistry
  108186. chemical
  108187. strateg
  108188. molecular
  108189. structure
  108190. organosilicon
  108191. compounds
  108192. molecule
  108193. molecules
  108194. molecules
  108195. large
  108196. cavities
  108197. supramolecular
  108198. chemistry
  108199. molecules-unusual
  108200. molinero
  108201. molinski
  108202. molinski
  108203. tadeusz
  108204. marine
  108205. pyridoacridine
  108206. alkaloids
  108207. structure
  108208. molloy
  108209. molloy
  108210. kieran
  108211. organotin
  108212. heterocycles
  108213. organometallic
  108214. molluscs
  108215. mollusks
  108216. molodova
  108217. molten
  108218. molybdenum
  108219. molybdenum/cobalt/su
  108220. moments
  108221. momicchioli
  108222. momose
  108223. momoyo
  108224. monakov
  108225. mondon
  108226. mondril
  108227. monensin
  108228. monforte
  108229. monica
  108230. moniliforme
  108231. moniliformin
  108232. moniot
  108233. monique
  108234. monitored
  108235. monitoring
  108236. moniz
  108237. moniz
  108238. poranski
  108239. sojka
  108240. cidnp
  108241. mechanist
  108242. monneret
  108243. monneret
  108244. florent
  108245. isosaccharino
  108246. glucosaccharino
  108247. mono-olefins
  108248. monoacetals
  108249. monoalkylation
  108250. monoalkyltriazenes
  108251. monoaminals
  108252. monoaminals
  108253. glyoxal
  108254. versatile
  108255. chirons
  108256. nocarbonic
  108257. monocarbonic
  108258. derivatives
  108259. simple
  108260. monocarbonic
  108261. deriv
  108262. monocarbonic
  108263. derivatives
  108264. cyano
  108265. function
  108266. monocarbonic
  108267. derivatives
  108268. cumulated
  108269. x-double
  108270. monocarbonyl
  108271. monocations
  108272. monocharides
  108273. monochloride
  108274. monoclonal
  108275. monocouplings
  108276. monocyclic
  108277. monocyclopentadienyl
  108278. monocyclopentadienyl
  108279. halide
  108280. complexes
  108281. f-block
  108282. monodisperse
  108283. monoenes
  108284. monofluorination
  108285. monofluoroaliphatic
  108286. monofunctional
  108287. monograph
  108288. monographs
  108289. monohalo
  108290. monoheterofunctional
  108291. monoheterofunctional
  108292. substituted
  108293. ketene
  108294. acetals
  108295. monoheterosubstitute
  108296. monoheterosubstitute
  108297. ketenes
  108298. thioketenes
  108299. ketenimines
  108300. monoimine
  108301. monoketals
  108302. monolayer
  108303. monolayers
  108304. monomer
  108305. monomeric
  108306. monomers
  108307. monomorine
  108308. mononitroarenes
  108309. mononuclear
  108310. mononuclear
  108311. dinuclear
  108312. pentamethylcyclopent
  108313. iron-carbene
  108314. monoolefin
  108315. monoolefins
  108316. monooxides
  108317. monoperoxy
  108318. monoperphthalate
  108319. monopersulfate
  108320. monophosphate
  108321. monophosphates
  108322. monophosphine
  108323. monophosphine-pallad
  108324. monosaccharide
  108325. monosaccharides
  108326. monosilylated
  108327. monostory
  108328. monosubstituted
  108329. monoterpene
  108330. monoterpenes
  108331. monoterpenoid
  108332. monoterpenoids
  108333. monothioketals
  108334. monothiopyrophosphat
  108335. monoxide
  108336. montanari
  108337. montanari
  108338. biomimetic
  108339. oxygenations
  108340. catalyzed
  108341. metallo
  108342. montanari
  108343. fernando
  108344. banfi
  108345. stefano
  108346. pozzi
  108347. gianluca
  108348. quici
  108349. silvio
  108350. montanine
  108351. monte
  108352. monteil
  108353. montforts
  108354. montforts
  108355. franz
  108356. peter
  108357. gerlach
  108358. benjamin
  108359. hoeper
  108360. frank
  108361. discover
  108362. montgomery
  108363. moody{
  108364. moody
  108365. andrew
  108366. fullerene
  108367. chemistry
  108368. chemistry
  108369. industry
  108370. moody
  108371. doyle
  108372. elliott
  108373. mowlem
  108374. synthesis
  108375. moody
  108376. synthesis
  108377. carbazole
  108378. alkaloids
  108379. synlett
  108380. moody
  108381. christopher
  108382. charles
  108383. thomas
  108384. robert
  108385. pyridoa
  108386. moonsun
  108387. moore
  108388. moore
  108389. zwittazido
  108390. cleavage
  108391. 197912125
  108392. accounts
  108393. chemical
  108394. moore
  108395. crafting
  108396. molecular
  108397. based
  108398. solids
  108399. moore
  108400. constituents
  108401. green
  108402. algae
  108403. marine
  108404. natural
  108405. moorefield
  108406. moorefield
  108407. charles
  108408. newkome
  108409. george
  108410. review
  108411. dendritic
  108412. mootoo
  108413. moravskii
  108414. morawetz
  108415. morawetz
  108416. reactivity
  108417. systems
  108418. containing
  108419. polymers
  108420. mordecai
  108421. mordini
  108422. mordini
  108423. alessandro
  108424. superbases
  108425. their
  108426. organic
  108427. synth
  108428. moreau
  108429. moreno
  108430. moreno
  108431. manas
  108432. marcial
  108433. pleixats
  108434. roser
  108435. bicyclic
  108436. compounds
  108437. struc
  108438. morera
  108439. moret
  108440. ammann
  108441. bissig
  108442. pretsch
  108443. simon
  108444. cation
  108445. selectiv
  108446. morga
  108447. morgan
  108448. morgunova
  108449. akira
  108450. takeshita
  108451. hitoshi
  108452. anodic
  108453. oxidation
  108454. synthe
  108455. synthetic
  108456. stereochemical
  108457. aspects
  108458. pheromone
  108459. synthetic
  108460. chemistry
  108461. insect
  108462. pheromones
  108463. juvenile
  108464. synthesis
  108465. insect
  108466. pheromones
  108467. total
  108468. miwako
  108469. syntheses
  108470. natural
  108471. products
  108472. using
  108473. zirconi
  108474. moriarty
  108475. moriarty
  108476. robert
  108477. radhe
  108478. koser
  108479. gerald
  108480. hydroxy
  108481. organo
  108482. morimoto
  108483. morimoto
  108484. toshiaki
  108485. chiba
  108486. mitsuo
  108487. achiwa
  108488. kazuo
  108489. development
  108490. morino
  108491. morin
  108492. chemistry
  108493. boron
  108494. analogs
  108495. biomolecules
  108496. tetrao
  108497. morisaki
  108498. morishima
  108499. morize
  108500. morken
  108501. morkovnik
  108502. morkovnik
  108503. okhlobystin
  108504. inorganic
  108505. radical
  108506. morozov
  108507. morphinandienone
  108508. morphinandienone
  108509. alkaloids
  108510. morphinans
  108511. morphine
  108512. morrill
  108513. morrin
  108514. morris
  108515. morrison
  108516. morrison
  108517. photochemistry
  108518. nonconjugated
  108519. olefins
  108520. morrison
  108521. photochemistry
  108522. organic
  108523. bichromophoric
  108524. molecule
  108525. morsi
  108526. mortimer
  108527. morton
  108528. moscow
  108529. mosettig
  108530. moskva
  108531. mosquera
  108532. carbenic
  108533. selectivity
  108534. cyclopropanation
  108535. reactions
  108536. jones
  108537. carbenes
  108538. reactive
  108539. intermediates
  108540. morkovnik
  108541. okhlobystin
  108542. inorganic
  108543. radical
  108544. jones
  108545. carbenes
  108546. reactive
  108547. intermediates
  108548. mukerjee
  108549. kumar
  108550. chemistry
  108551. dihydro
  108552. multifunctional
  108553. munawer
  108554. murray
  108555. mutasynthesis@
  108556. imines
  108557. related
  108558. hetero
  108559. dienes
  108560. cycloaddition@
  108561. kornblum
  108562. angew
  108563. substitution
  108564. reacti@
  108565. bednyagina
  108566. postovskii
  108567. garnovskii
  108568. osipov@
  108569. n'-tetramethyletylen@
  108570. n-carboxylic@
  108571. n-dimethylhydrazones@
  108572. nagata
  108573. saito
  108574. selective
  108575. oxidations
  108576. peroxide
  108577. based@
  108578. nakano
  108579. synthesis
  108580. biological
  108581. activities
  108582. mitomycin
  108583. naphthalene
  108584. nasipuri
  108585. stereochemistry
  108586. organic
  108587. compounds
  108588. principles
  108589. natural
  108590. natural
  108591. products
  108592. synthesis
  108593. palytoxin@
  108594. naumann
  108595. chemistry
  108596. synthetic
  108597. pyrethrium
  108598. insecticides
  108599. nefedov
  108600. jones
  108601. carbenes
  108602. reactive
  108603. intermediates
  108604. robert
  108605. absolute
  108606. kinetics
  108607. intramolecular
  108608. alklycarbe
  108609. mossbauer
  108610. mostly
  108611. motallebi
  108612. motherwell
  108613. motherwell
  108614. nutley
  108615. carbenoids
  108616. motherwell
  108617. william
  108618. curiosity
  108619. driven
  108620. research
  108621. motherwell
  108622. william
  108623. crich
  108624. david
  108625. radical
  108626. chain
  108627. reaction
  108628. motion
  108629. motohashi
  108630. motohashi
  108631. kawase
  108632. emrani
  108633. synthesis
  108634. carcinogenic
  108635. motohiro
  108636. motoji
  108637. motokazu
  108638. motoyoshiya
  108639. motuporin
  108640. motyka
  108641. moule
  108642. moulines
  108643. mountford
  108644. mousawi
  108645. mouser
  108646. moussiaux
  108647. moutet
  108648. moutet
  108649. claude
  108650. electrocatalytic
  108651. hydrogenation
  108652. hydroge
  108653. mouzin
  108654. movsum
  108655. movsum
  108656. preparation
  108657. reactions
  108658. chloro
  108659. derivati
  108660. mowlem
  108661. moye|
  108662. mozingo
  108663. mpoumds
  108664. mpounds
  108665. mrejen
  108666. ms-free
  108667. ms/ms
  108668. muccino
  108669. muchowski
  108670. muchowski
  108671. joseph
  108672. development
  108673. ketorolac
  108674. impact
  108675. mucklejohn
  108676. mucus
  108677. mueller
  108678. mueller
  108679. felix
  108680. mattay
  108681. jochen
  108682. photocycloadditions
  108683. control
  108684. mueller
  108685. westerhoff
  108686. ulrich
  108687. vance
  108688. blake
  108689. muetterties
  108690. muetterties
  108691. bleeke
  108692. catalytic
  108693. hydrogenation
  108694. aromat
  108695. muetterties
  108696. stein
  108697. mechanistic
  108698. features
  108699. catalytic
  108700. muhammad
  108701. mukai
  108702. mukai
  108703. kumagai
  108704. yamashita
  108705. cyclization
  108706. cycloaddition
  108707. mukaiyama
  108708. mukaiyama
  108709. synthetic
  108710. reactions
  108711. based
  108712. onium
  108713. salts
  108714. mukaiyami
  108715. mukaiyami
  108716. matsueda
  108717. oxidation
  108718. reduction
  108719. conden
  108720. mukayiama
  108721. mukerjee
  108722. mukerjee
  108723. kumar
  108724. chemistry
  108725. dihydro
  108726. mukerjee
  108727. singh
  108728. lactams
  108729. retrospect
  108730. prospect
  108731. mukhametshin
  108732. mukhametshin
  108733. advances
  108734. chemistry
  108735. organofluorine
  108736. mukund
  108737. mulberry
  108738. mulhaupt
  108739. mullen
  108740. mullen
  108741. carbonylations
  108742. catalyzed
  108743. metal
  108744. carbonyls/reppe
  108745. mullen
  108746. closure
  108747. reactions
  108748. carbon
  108749. monoxide
  108750. muller
  108751. muller
  108752. martin
  108753. seebach
  108754. dieter
  108755. hydroxybutanoates
  108756. muller
  108757. spectra
  108758. organic
  108759. chemistry
  108760. mulquiney
  108761. multi
  108762. multi-stage
  108763. multibridged
  108764. multicomponent
  108765. multicomponent
  108766. one-pot
  108767. annulations
  108768. forming
  108769. bonds
  108770. multiconfigurational
  108771. multidentate
  108772. multidimensional
  108773. multielectron
  108774. multifidene
  108775. multifunctional
  108776. multifunctional
  108777. multifunctional
  108778. amino
  108779. acids
  108780. their
  108781. incorporation
  108782. pepti
  108783. multilayer
  108784. multilayered
  108785. multimetallic
  108786. multinuclear
  108787. multinuclear
  108788. using
  108789. lanthanide
  108790. shift
  108791. reagents
  108792. analy
  108793. multiphase
  108794. multiple
  108795. multiple
  108796. peptide
  108797. synthesis
  108798. methods
  108799. their
  108800. applications
  108801. multiple
  108802. stereocontrol
  108803. using
  108804. organometallic
  108805. complexes
  108806. applic
  108807. multiplet
  108808. multiplication
  108809. multiply
  108810. multiply
  108811. bonded
  108812. germanium
  108813. species
  108814. recent
  108815. developments
  108816. multipurpose
  108817. multistage
  108818. multistep
  108819. multistepped
  108820. mulzer
  108821. mulzer
  108822. johann
  108823. erythromycin
  108824. synthesis
  108825. never
  108826. ending
  108827. story
  108828. munawer
  108829. munawer
  108830. mundy
  108831. mundy
  108832. concepts
  108833. organic
  108834. synthesis
  108835. carbocyclic
  108836. chemistr
  108837. munoz
  108838. munslow
  108839. muons
  108840. murahashi
  108841. murahashi
  108842. naota
  108843. takeshi
  108844. ruthenium
  108845. catalyzed
  108846. oxidat
  108847. murahashi
  108848. shunichi
  108849. biomimetic
  108850. oxidation
  108851. organic
  108852. synthesis
  108853. murai
  108854. murai
  108855. sonoda
  108856. catalytic
  108857. reactions
  108858. hydrosilame
  108859. murakami
  108860. murakami
  108861. kikuchi
  108862. supramolecular
  108863. assemblies
  108864. formed
  108865. murakami
  108866. yukito
  108867. hayashida
  108868. osamu
  108869. hisaeda
  108870. yoshio
  108871. muralidhara
  108872. muramyl
  108873. muramyl
  108874. peptides
  108875. lipopeptides
  108876. studies
  108877. towards
  108878. immunostim
  108879. murat
  108880. murata
  108881. murata
  108882. ichiro
  108883. novel
  108884. bonding
  108885. structure
  108886. nonalternant
  108887. murav'eva
  108888. muriel
  108889. murphree
  108890. murphy
  108891. murphy
  108892. grif3lths
  108893. survey
  108894. natural
  108895. products
  108896. which
  108897. murray
  108898. murray
  108899. murray
  108900. naturally
  108901. occurring
  108902. plant
  108903. coumarins
  108904. murray
  108905. naturally
  108906. occurring
  108907. plant
  108908. coumarins
  108909. murray
  108910. chemical
  108911. sources
  108912. singlet
  108913. oxygen
  108914. singlet
  108915. oxygen
  108916. murray
  108917. william
  108918. angiotensin
  108919. receptorantagonists
  108920. murrell
  108921. murrell
  108922. tedder
  108923. chemical
  108924. wiley
  108925. interscience
  108926. murthy
  108927. murugan
  108928. murugan
  108929. grendze
  108930. toomey
  108931. katritzky
  108932. karelson
  108933. muscaria
  108934. muscarine
  108935. muscarine
  108936. oxazole
  108937. imidazole
  108938. thiazole
  108939. peptide
  108940. aloids
  108941. muscone
  108942. mushina
  108943. mushrooms
  108944. musker
  108945. musker
  108946. chemistry
  108947. aliphatic
  108948. thioether
  108949. cation
  108950. radicals
  108951. musso
  108952. musso
  108953. pigments
  108954. agaric
  108955. amanita
  108956. muscaria
  108957. musumarra
  108958. muszkat
  108959. muszkat
  108960. dihydrophenanthrenes
  108961. topics
  108962. mutagenic
  108963. mutai
  108964. mutasynthesis
  108965. mutter
  108966. mutter
  108967. bayer
  108968. liquid
  108969. phase
  108970. method
  108971. peptide
  108972. synthes
  108973. muzaffar
  108974. muzart
  108975. muzart
  108976. chromium
  108977. catalyzed
  108978. oxidations
  108979. organic
  108980. synthesis
  108981. muzart
  108982. jacques
  108983. silyl
  108984. ethers
  108985. protective
  108986. groups
  108987. alcohol
  108988. myagkova
  108989. mycaroside
  108990. mycotoxin
  108991. mycotoxins
  108992. myers
  108993. myers
  108994. richard
  108995. lourdes
  108996. rivier
  108997. olivera
  108998. baldome
  108999. myles
  109000. mynott
  109001. myo-inositol
  109002. myriocin
  109003. myrocin
  109004. mystery
  109005. myxothiazols
  109006. dilithioalkylamines
  109007. aziridines
  109008. naphthalene
  109009. catal
  109010. aziridines
  109011. acylating
  109012. agents
  109013. preparation
  109014. imines
  109015. related
  109016. hetero
  109017. dienes
  109018. cycloaddition
  109019. acylimines
  109020. related
  109021. hetero
  109022. dienes
  109023. cycloaddition
  109024. alkylation
  109025. electrophilic
  109026. substitution
  109027. reactions
  109028. alkylation
  109029. aromatic
  109030. heteroaromatic
  109031. dinitrophenyl
  109032. alkylation
  109033. nitrogen
  109034. azoles
  109035. amino
  109036. aziridine
  109037. hydrazones
  109038. highly
  109039. diastereoselective
  109040. alkyl
  109041. aminoaziridinylhydra
  109042. highly
  109043. diastereoselective
  109044. alkylation
  109045. balasubramanian
  109046. proced
  109047. recent
  109048. balasuframanian
  109049. recent
  109050. synthet
  109051. baird
  109052. initio
  109053. calculations
  109054. photochemistry
  109055. calderon
  109056. olefin
  109057. metathesis
  109058. reaction
  109059. chemistry
  109060. cohen
  109061. accounts
  109062. asymmetric
  109063. induction
  109064. epiotis
  109065. cherry
  109066. shaik
  109067. yates
  109068. bernardi
  109069. struct
  109070. shvetsov
  109071. shilovskii
  109072. bobkova
  109073. ignatova
  109074. iodosuccinimide
  109075. superior
  109076. reagent
  109077. generation
  109078. kornblum
  109079. angew
  109080. substitution
  109081. reacti
  109082. bauld
  109083. cation
  109084. radical
  109085. bauld
  109086. mechanistic
  109087. alpatova
  109088. zabusova
  109089. tomilov
  109090. nibbering
  109091. phase
  109092. organic
  109093. przheval'skii
  109094. grandberg
  109095. metalated
  109096. azomethine
  109097. ylides
  109098. metallo
  109099. imines
  109100. synthesis
  109101. aziridines
  109102. trimethylsil
  109103. reagents
  109104. variety
  109105. reaction
  109106. modes
  109107. trimethylsilyl
  109108. ynamines
  109109. cycloaddition
  109110. reactions
  109111. cleavage
  109112. rearrangements
  109113. arylhydrazones
  109114. tetramethylazodicarb
  109115. versatile
  109116. reagent
  109117. n'-bis
  109118. 222-trifluoroethyl
  109119. n'-ethylenetartramid
  109120. improv
  109121. synthesis
  109122. reductive
  109123. cleavage
  109124. organometallic
  109125. prostaglandins
  109126. three-component
  109127. bednyagina
  109128. postovskii
  109129. garnovskii
  109130. osipov
  109131. shusherina
  109132. diene
  109133. synthesis
  109134. petragnani
  109135. comasseto
  109136. synthesis
  109137. synthetic
  109138. petragnani
  109139. ferraz
  109140. silva
  109141. synthesis
  109142. rayyes
  109143. awadi
  109144. synthesis
  109145. synthe
  109146. rabjohn
  109147. selenium
  109148. dioxide
  109149. oxidation
  109150. organic
  109151. enikolpyan
  109152. catalysis
  109153. metall
  109154. isaacs
  109155. synthetic
  109156. routes
  109157. zefirov
  109158. koz'min
  109159. competit
  109160. zefirov
  109161. problem
  109162. conformational
  109163. effects
  109164. substituted
  109165. pyrrolinones
  109166. enamines
  109167. dicarbonyls
  109168. butoxycarbonyl
  109169. butyldimethylsiloxy
  109170. pyrrole
  109171. averina
  109172. zefirov
  109173. advanc
  109174. alkylation
  109175. mitsunobu
  109176. reaction
  109177. pyridone
  109178. n'-bis
  109179. n'-ethylenetartramid
  109180. n'-tetramethylethyle
  109181. n'-tetramethyletylen
  109182. n-4-alkenylhydroxyla
  109183. n-acetals
  109184. n-acetoacetylated
  109185. n-acetylneuraminic
  109186. n-acyl
  109187. n-acyl
  109188. imines
  109189. related
  109190. heterodienes
  109191. cycloaddition
  109192. n-acyl-a-methoxyamin
  109193. n-acylhydrazonium
  109194. n-acyliminium
  109195. n-acyliminium
  109196. intermediates
  109197. alkaloid
  109198. synthesis
  109199. n-acyllactams
  109200. n-acylnitroso
  109201. n-alkyl
  109202. n-alkyl/arylimidic
  109203. n-alkyl/arylimidic
  109204. esters
  109205. hydroximic
  109206. acids
  109207. alkyl
  109208. hydrazonate
  109209. n-alkylation
  109210. n-alkylation
  109211. nitrogen
  109212. azoles
  109213. n-alkylpyridinium
  109214. n-aminoazoles
  109215. n-arylamines
  109216. n-bis-tosylhydrazone
  109217. n-boc-cbi
  109218. n-boc-cbq
  109219. n-boc-n-methylbenzyl
  109220. n-boc-pyrrolidines
  109221. n-bond
  109222. n-butyllithium
  109223. n-derivatives
  109224. n-dialkyl-13-dien-1
  109225. n-dialkylarylamines
  109226. n-dienyl
  109227. n-dienyl
  109228. amides
  109229. lactams
  109230. preparation
  109231. diels-alder
  109232. n-dihaloamines
  109233. n-dimethylhydrazones
  109234. n-enoyloxazolinones
  109235. n-functional
  109236. n-functionalized
  109237. n-functionalized
  109238. carbodiimides
  109239. n-glucoaspargine
  109240. n-dihaloamines
  109241. n-haloamide
  109242. n-halogeno
  109243. n-halogeno-n-metallo
  109244. n-haloimines
  109245. n-heterocyclic
  109246. n-hydroxy
  109247. n-hydroxy
  109248. amino
  109249. acids
  109250. their
  109251. derivatives
  109252. n-hydroxyimides
  109253. n-imides
  109254. n-lithiated
  109255. n-metalated
  109256. n-metalated
  109257. azomethine
  109258. ylides
  109259. n-methoxy-n-methylam
  109260. n-methyl-a-amino
  109261. n-methylindole
  109262. reagents
  109263. variety
  109264. reaction
  109265. modes
  109266. n-nitroamines
  109267. n-nitroimines
  109268. n-nitroso
  109269. n-nitrosoamines
  109270. n-nitrosoimines
  109271. n-oxides
  109272. n-pentenyl
  109273. n-pentenyl
  109274. glycosides
  109275. organic
  109276. chemistry
  109277. contemporary
  109278. n-phenylindole
  109279. n-phosphorylated
  109280. n-phosphorylated
  109281. amides
  109282. thioamides
  109283. n-protected
  109284. n-substituted
  109285. n-substituted
  109286. n-substituted
  109287. pyridinium
  109288. salts
  109289. n-sulfides
  109290. n-sulfides
  109291. dinitrogen
  109292. lfide
  109293. thiofulminic
  109294. nitrile
  109295. n-sulfonyloxaziridin
  109296. n-sulinyl
  109297. n-sulphinyl
  109298. n/n-acetals
  109299. nabh4
  109300. nabivach
  109301. nabivach
  109302. dmitrikov
  109303. correlation
  109304. equations
  109305. naddaka
  109306. mimics
  109307. stereos
  109308. lective
  109309. reduction
  109310. benzoylform
  109311. nadler
  109312. naeff
  109313. naeff
  109314. franssen
  109315. maurice
  109316. quant
  109317. naelong
  109318. nafion
  109319. nafion-h
  109320. nafti
  109321. nagahara
  109322. nagai
  109323. nagai
  109324. hydrosilanes
  109325. reducing
  109326. agents
  109327. 19801213
  109328. organic
  109329. nagano
  109330. nagao
  109331. nagapetyan
  109332. nagarajam
  109333. nagarajan
  109334. nagase
  109335. nagase
  109336. shigeru
  109337. theoretical
  109338. study
  109339. heteroatom
  109340. containing
  109341. nagashima
  109342. nagata
  109343. nagata
  109344. saito
  109345. selective
  109346. oxidations
  109347. peroxide
  109348. based
  109349. nagata
  109350. yoshioka
  109351. hydrocyanation
  109352. conjugated
  109353. carbonyl
  109354. nagel
  109355. nageshwar
  109356. nagilactone
  109357. nagle
  109358. nagubandi
  109359. nagwa
  109360. azirines
  109361. small
  109362. heterocycles
  109363. chemistry
  109364. heteroc
  109365. naito
  109366. nakagaki
  109367. nakagaki
  109368. ryoichi
  109369. tanimoto
  109370. yoshifumi
  109371. mutai
  109372. kiyoshi
  109373. magnetic
  109374. nakagawa
  109375. nakagawa
  109376. annulenoannulenes
  109377. 197918
  109378. angewandte
  109379. chemie
  109380. nakagawa
  109381. naito
  109382. kawaguchi
  109383. structures
  109384. nakai
  109385. nakamura
  109386. nakamura
  109387. eiichi
  109388. tools
  109389. synthetic
  109390. organocopper
  109391. chemistr
  109392. nakanishi
  109393. nakanishi
  109394. wandering
  109395. natural
  109396. products
  109397. chemist
  109398. profiles
  109399. nakanishi
  109400. dimensional
  109401. dimensional
  109402. nakano
  109403. nakano
  109404. synthesis
  109405. biological
  109406. activities
  109407. mitomycin
  109408. nakasuji
  109409. nakasuki
  109410. nakata
  109411. nakatani
  109412. nakatani
  109413. fukuda
  109414. terashima
  109415. synthesis
  109416. cytotoxicity
  109417. nakayama
  109418. nakazaki
  109419. naked
  109420. naked
  109421. fluoride
  109422. chemistry
  109423. review
  109424. available
  109425. reagents
  109426. naked
  109427. fluoride
  109428. chemistry
  109429. technique
  109430. desilylation
  109431. nakhshunov
  109432. nakova
  109433. nakshatra
  109434. nalcolm
  109435. reactio
  109436. reagents
  109437. organic
  109438. synthesis
  109439. nametkin
  109440. namor
  109441. nanasi
  109442. nancy
  109443. nangia
  109444. nanjappan
  109445. nanjundiah
  109446. nanochemistry
  109447. nanoscopic
  109448. nanostructures
  109449. nantermet
  109450. naofumi
  109451. naoki
  109452. naomi
  109453. naomichi
  109454. naota
  109455. naphthacenequinones
  109456. naphthacenequinones
  109457. synthesis
  109458. properties
  109459. naphthalene
  109460. naphthalene
  109461. naphthalene
  109462. catalysed
  109463. reductive
  109464. desulfonylation
  109465. lithium
  109466. naphthalene
  109467. catalyzed
  109468. reductive
  109469. opening
  109470. aziridines
  109471. naphthalenes
  109472. naphthalenide
  109473. naphthalic
  109474. naphthazarins
  109475. naphthenes
  109476. naphthimidazopyridin
  109477. naphthindolizine
  109478. naphtho
  109479. naphthoquinone
  109480. naphthoquinones
  109481. naphthyl
  109482. naphthylethyl
  109483. naphthyridine
  109484. naphthyridines
  109485. naphthyridines
  109486. pyridoquinolines
  109487. anthyridines
  109488. similar
  109489. naphthyridinomycin
  109490. napieraiski
  109491. napieralski
  109492. naqvi
  109493. narang
  109494. narasaka
  109495. narasaka
  109496. koichi
  109497. chiral
  109498. reagents
  109499. asymmetric
  109500. construction
  109501. narayan
  109502. narayana
  109503. narendra
  109504. naresh
  109505. narisada
  109506. narisawa
  109507. narisimban
  109508. narita
  109509. nartsada
  109510. narula
  109511. naruse
  109512. naruta
  109513. nascimento
  109514. nasipuri
  109515. nasipuri
  109516. stereochemistry
  109517. organic
  109518. compounds
  109519. principles
  109520. nasirova
  109521. nasirova
  109522. murav'eva
  109523. mushina
  109524. krentsel
  109525. nastasi
  109526. nastasi
  109527. streith
  109528. photochemical
  109529. rearrangements
  109530. involving
  109531. natale
  109532. natale
  109533. nicholas
  109534. mirzaei
  109535. yousef
  109536. lateral
  109537. metalation
  109538. natalia
  109539. natalie
  109540. natarajan
  109541. nathan
  109542. nather
  109543. nation
  109544. national
  109545. natori
  109546. natori
  109547. ikekawa
  109548. suzuki
  109549. advances
  109550. natural
  109551. products
  109552. natta
  109553. naturalV
  109554. natural
  109555. natural
  109556. oxycarbonyloxaz
  109557. natural
  109558. products
  109559. reports
  109560. protonated
  109561. protosolvated
  109562. natural
  109563. products
  109564. reports
  109565. recent
  109566. advances
  109567. natural
  109568. products
  109569. synthesis
  109570. palytoxin
  109571. natural
  109572. sesquiterpenoids
  109573. natural-products
  109574. naturally
  109575. naturally
  109576. ccuring
  109577. peroxides
  109578. naturally
  109579. occurring
  109580. 12-dithiins
  109581. naturally
  109582. occurring
  109583. 12-dithiolanes
  109584. 123-trithianes
  109585. chemic
  109586. naturally
  109587. occurring
  109588. 6-substituted
  109589. 56-dihydro-alpha-pyr
  109590. naturally
  109591. occurring
  109592. benzodiazepines
  109593. structure
  109594. distribution
  109595. naturally
  109596. occurring
  109597. trithiophenes
  109598. naturally
  109599. occurring
  109600. mevinic
  109601. acids
  109602. synthetic
  109603. studies
  109604. naturally
  109605. occurring
  109606. plant
  109607. coumarins
  109608. nature
  109609. nature'sm
  109610. naumann
  109611. naumann
  109612. chemistry
  109613. synthetic
  109614. pyrethrium
  109615. insecticides
  109616. nawracka
  109617. nayak
  109618. naylor
  109619. nayyar
  109620. nazarenko
  109621. nazario
  109622. nazarov
  109623. nazarov
  109624. related
  109625. cationic
  109626. cyclizations
  109627. nazarov
  109628. cyclization
  109629. review
  109630. nazer
  109631. nazin
  109632. nazin
  109633. manelis
  109634. thermal
  109635. decomposition
  109636. aliphatic
  109637. nazran
  109638. thilivhali
  109639. warner
  109640. isiah
  109641. applications
  109642. multidimens
  109643. nearly
  109644. nebenzahl
  109645. necessity
  109646. neckers
  109647. neckers
  109648. douglas
  109649. valdes
  109650. aguilera
  109651. oscar
  109652. photochemistry
  109653. nedel'kin
  109654. nedelec
  109655. nedolya
  109656. nedolya
  109657. trofimov
  109658. sulfur
  109659. containing
  109660. vinyl
  109661. ethers
  109662. nedolya
  109663. trofimov
  109664. sulfur
  109665. derivatives
  109666. vinyl
  109667. ethers
  109668. needles
  109669. neena
  109670. neenan
  109671. neenan
  109672. thomas
  109673. miller
  109674. timothy
  109675. kwock
  109676. elizabeth
  109677. nefedov
  109678. nefedov
  109679. nefedov
  109680. d'yachenko
  109681. prokof'ev
  109682. arynes
  109683. carbenes
  109684. nefedov
  109685. egorov
  109686. ioffe
  109687. menchikov
  109688. nefedov
  109689. sinotova
  109690. lebedev
  109691. vinyl
  109692. cations
  109693. negative
  109694. negishi
  109695. negishi
  109696. organometallics
  109697. organic
  109698. synthesis
  109699. wiley
  109700. negishi
  109701. selective
  109702. carbon
  109703. carbon
  109704. formation
  109705. trans
  109706. negishi
  109707. takahashi
  109708. tamotsu
  109709. patterns
  109710. stoichiometric
  109711. negishi
  109712. takahashi
  109713. tamotsu
  109714. zirconocene
  109715. alkene
  109716. complex
  109717. negishi
  109718. eiichi
  109719. zipper
  109720. cascade
  109721. carbometalation
  109722. const
  109723. neglected
  109724. negoro
  109725. negoro
  109726. takeshi
  109727. shigeru
  109728. ligand
  109729. coupling
  109730. hypervalent
  109731. negrebetskii
  109732. negri
  109733. neighboring
  109734. neighboring
  109735. group
  109736. participation
  109737. lewis
  109738. promoted
  109739. neighbouring
  109740. neighbouring
  109741. neighbouring
  109742. group
  109743. participation
  109744. carbonyl
  109745. groups
  109746. ester
  109747. neighbouring
  109748. group
  109749. participation
  109750. lewis
  109751. acid-promoted
  109752. neiland
  109753. neilands
  109754. nelke
  109755. nelsen
  109756. nelsen
  109757. conformational
  109758. studies
  109759. hexahydropyridazine
  109760. deriv
  109761. nelsen
  109762. electron
  109763. oxidation
  109764. tetraalkylhydrazines
  109765. nelsen
  109766. stephen
  109767. internal
  109768. geometry
  109769. relaxation
  109770. effects
  109771. nelson
  109772. nemes
  109773. nemeth
  109774. nemoto
  109775. nenitzescu
  109776. neocarzinostatin
  109777. neocarzinostatine
  109778. neoglycoconjugatesP
  109779. neoglycoproteins
  109780. neolemnane
  109781. neolignans
  109782. neonatal
  109783. neopentyl
  109784. neoplasms
  109785. neotropical
  109786. neous
  109787. nephrosteranic
  109788. nesmeyanov
  109789. nesmeyanov
  109790. rybinskaya
  109791. rybin
  109792. dinuclear
  109793. carbo
  109794. nesper
  109795. neighbouring
  109796. neocryptotanshinone@
  109797. nesper
  109798. reinhard
  109799. fullercages
  109800. without
  109801. fulleranes
  109802. fulle@
  109803. neutral
  109804. acyclic
  109805. analogues
  109806. crown-ethers
  109807. cryptands
  109808. access
  109809. fused
  109810. vinylcyclopropanes
  109811. radical
  109812. cyclizatio@
  109813. aromatic
  109814. substitution@
  109815. recent
  109816. developments
  109817. research
  109818. multi-stage
  109819. redox
  109820. systems
  109821. organic
  109822. molecular
  109823. meta@
  109824. reactions
  109825. involving
  109826. oxidative
  109827. phosphorylat@
  109828. synthesis
  109829. azaheterocycles
  109830. rearrangement
  109831. isoxazo@
  109832. tailored
  109833. hosts
  109834. molecular
  109835. recognition
  109836. mechanical
  109837. newjersey@
  109838. nicholas
  109839. nestle
  109840. seyferth
  109841. potential
  109842. utility
  109843. nickel-catalysed
  109844. niecke@
  109845. nitrile
  109846. nitro
  109847. nitrocycloalkenes@
  109848. nitrogen
  109849. nitrones
  109850. nitta
  109851. makoto
  109852. reactions
  109853. vinylimino
  109854. phosphoranes
  109855. relate@
  109856. nesper
  109857. reinhard
  109858. fullercages
  109859. without
  109860. fulleranes
  109861. fulle
  109862. nestle
  109863. nesunts
  109864. netherlandsV
  109865. netropsin
  109866. netto
  109867. nettoferreira
  109868. networks
  109869. neuenschwander
  109870. neumann
  109871. neumann
  109872. wilhelm
  109873. germylenes
  109874. stannylenes
  109875. neunhoffer
  109876. neunhoffer
  109877. wiley
  109878. chemistry
  109879. triazines
  109880. neurophysins
  109881. neuss
  109882. neutral
  109883. acyclic
  109884. analogues
  109885. crown-ethers
  109886. cryptands
  109887. neutralization
  109888. neutrals
  109889. neutron
  109890. never
  109891. neveux
  109892. reagents
  109893. across
  109894. advances
  109895. chemistry
  109896. thiirans
  109897. allyl
  109898. group
  109899. acceptors
  109900. palladium
  109901. catalyzed
  109902. removal
  109903. alternatives
  109904. oxidative
  109905. phenolic
  109906. coupli
  109907. natural
  109908. amino-protecting
  109909. groups
  109910. organic
  109911. synthesis
  109912. applications
  109913. organopalladium
  109914. compounds
  109915. organic
  109916. applications
  109917. periodic
  109918. periodates
  109919. organic
  109920. applications
  109921. tetracyanoethylene
  109922. organometallic
  109923. approach
  109924. natural
  109925. product
  109926. synthesis
  109927. using
  109928. group
  109929. approaches
  109930. asymmetric
  109931. synthesis
  109932. using
  109933. gamma-alkoxybut
  109934. approaches
  109935. amino
  109936. acids
  109937. chiral
  109938. building
  109939. approaches
  109940. amino
  109941. acids
  109942. chiral
  109943. building
  109944. aspects
  109945. carbonylation
  109946. reactions
  109947. catalyzed
  109948. transiti
  109949. aspects
  109950. glycosylation
  109951. reactions
  109952. aspects
  109953. reactions
  109954. cations
  109955. radicals
  109956. heteroc
  109957. aspects
  109958. organocopper
  109959. reagents
  109960. 12-chiral
  109961. induct
  109962. aspects
  109963. organocopper
  109964. reagents
  109965. chiral
  109966. induction
  109967. aspects
  109968. oxypalladation
  109969. alkenes
  109970. aspects
  109971. stereoselective
  109972. synthesis
  109973. 13-polyols
  109974. asymmetric
  109975. route
  109976. bridged
  109977. indole
  109978. alkaloids
  109979. formal
  109980. naphthalic
  109981. anhydrides
  109982. polyheteroarylenes
  109983. based
  109984. bridgehead
  109985. nitrogen
  109986. heterocycles
  109987. furan
  109988. potent
  109989. carbonylations
  109990. means
  109991. transition
  109992. metal
  109993. catalysts
  109994. chemistry
  109995. oxazoles
  109996. chemistry
  109997. oxazoles
  109998. review
  109999. chiral
  110000. b-phosphinocarboxyli
  110001. acids
  110002. their
  110003. application
  110004. chirality
  110005. recognizing
  110006. reagents
  110007. determination
  110008. cyclopropyl
  110009. building
  110010. blocks
  110011. organic
  110012. synthesis
  110013. development
  110014. indole
  110015. alkaloids
  110016. developments
  110017. indole
  110018. alkaloids
  110019. developments
  110020. macrocyclic
  110021. polyamine
  110022. chemistry
  110023. developments
  110024. molecular
  110025. chirality
  110026. developments
  110027. chemistry
  110028. catalytic
  110029. antibodies
  110030. developments
  110031. field
  110032. photochemical
  110033. syntheses
  110034. diels-alder
  110035. reactions
  110036. vinylindoles
  110037. regio-and
  110038. dimensions
  110039. indole
  110040. chemistry
  110041. dimensions
  110042. indole
  110043. chemistry
  110044. ligand
  110045. design
  110046. directions
  110047. nucleophilic
  110048. aromatic
  110049. substitution
  110050. efficient
  110051. routes
  110052. cyclic
  110053. enediynes
  110054. entry
  110055. chiral
  110056. butenolide
  110057. synthons
  110058. application
  110059. exped
  110060. evidence
  110061. involvement
  110062. alkylidene
  110063. carbenes
  110064. findings
  110065. arene
  110066. chemistry
  110067. transition
  110068. fluori
  110069. ating
  110070. agents
  110071. organic
  110072. synthesis
  110073. formation
  110074. pyrrolizines
  110075. intramolecular
  110076. cyclization
  110077. formyl
  110078. anion
  110079. cation
  110080. equivalents
  110081. radical
  110082. syntheses
  110083. under
  110084. barton
  110085. oxidation
  110086. condit
  110087. general
  110088. methods
  110089. involving
  110090. allyl
  110091. palladium
  110092. complexes
  110093. general
  110094. synthetic
  110095. methods
  110096. involving
  110097. allylpalladium
  110098. compl
  110099. generation
  110100. 13-dipoles
  110101. organosilicon
  110102. compounds
  110103. horizons
  110104. carbonyl
  110105. chemistry
  110106. reagents
  110107. nucleophilic
  110108. insights
  110109. mechanism
  110110. photocycloaddit
  110111. insights
  110112. structure
  110113. oranocuprate
  110114. p-complexes
  110115. topics
  110116. recent
  110117. developments
  110118. research
  110119. structure
  110120. biosynthesis
  110121. cyclopro
  110122. ligands
  110123. improved
  110124. enantioselectives
  110125. asymmetri
  110126. mechanistic
  110127. insights
  110128. reduction
  110129. halides
  110130. radic
  110131. mechanistic
  110132. insights
  110133. reductions
  110134. halides
  110135. metalation
  110136. synthetic
  110137. applications
  110138. isonitriles
  110139. method
  110140. generation
  110141. alkenylidene
  110142. carbenes
  110143. method
  110144. generation
  110145. alkylidenecarbenes
  110146. proparg
  110147. method
  110148. preparation
  110149. alkoxycarbene
  110150. complexes
  110151. methods
  110152. strategies
  110153. stereocontrolled
  110154. synthesi
  110155. methods
  110156. control
  110157. multiple
  110158. stereocenters
  110159. methods
  110160. synthesis
  110161. glycosides
  110162. oligosacchar
  110163. methods
  110164. synthesis
  110165. troponoid
  110166. compounds
  110167. methods
  110168. arylation
  110169. methods
  110170. synthesis
  110171. linear
  110172. functionalized
  110173. isopreno
  110174. multi-stage
  110175. redox
  110176. systems
  110177. organic
  110178. molecular
  110179. organometallic
  110180. reagents
  110181. olefin
  110182. synthesis
  110183. organometallic
  110184. reagents
  110185. trimethylsilyl
  110186. thiazole
  110187. organoselenium
  110188. methodology
  110189. oxazolidinone
  110190. chiral
  110191. auxiliaries
  110192. intramolecular
  110193. perspectives
  110194. asymmetric
  110195. induction
  110196. perspectives
  110197. boron-nitrogen
  110198. chemistry
  110199. perspectives
  110200. formation
  110201. grignard
  110202. reagent
  110203. perspectives
  110204. carbo
  110205. hetero-13-dienes
  110206. organic
  110207. perspectives
  110208. carbene
  110209. rearrangements
  110210. migratory
  110211. aptitud
  110212. photochemistry
  110213. 25-cyclohexadien-1-o
  110214. related
  110215. compo
  110216. possible
  110217. applications
  110218. heavy
  110219. metal
  110220. main-group
  110221. elements
  110222. properties
  110223. reagents
  110224. complexation
  110225. carbanions
  110226. prototropic
  110227. processes
  110228. synthesis
  110229. heterocycles
  110230. pyrazoline
  110231. derivatives
  110232. radical
  110233. mediated
  110234. polyolefin
  110235. cyclisations
  110236. directed
  110237. toward
  110238. reactions
  110239. involving
  110240. oxidative
  110241. phosphorylat
  110242. reactions
  110243. involving
  110244. oxidative
  110245. c-phosphorylat
  110246. reactions
  110247. alkylidienephosphora
  110248. their
  110249. preparative
  110250. reactions
  110251. cyanic
  110252. esters
  110253. opening
  110254. reaction
  110255. thiiranes
  110256. carboxylic
  110257. routes
  110258. phosphorus
  110259. three
  110260. four-membered
  110261. routes
  110262. selectively
  110263. methylated
  110264. benzimidazoles
  110265. simple
  110266. iodoacetoxylation
  110267. alkenes
  110268. eight
  110269. membered
  110270. formation
  110271. based
  110272. intram
  110273. stereoselective
  110274. synthesis
  110275. trans
  110276. disubstituted
  110277. strategies
  110278. stereoselective
  110279. synthesis
  110280. natural
  110281. strategies
  110282. synthesis
  110283. beta-d-galacto-oligo
  110284. strategy
  110285. synthesis
  110286. taxane
  110287. diterpenes
  110288. synthesis
  110289. substituted
  110290. aminoethyl
  110291. indoles
  110292. synthesis
  110293. amino
  110294. carboxy
  110295. anhydrides
  110296. through
  110297. synthesis
  110298. azaheterocycles
  110299. rearrangement
  110300. isoxazo
  110301. synthetic
  110302. applications
  110303. dialkylboron
  110304. halide
  110305. reagents
  110306. synthetic
  110307. applications
  110308. oxycarbonylnitrenes
  110309. synthetic
  110310. applications
  110311. dithioacetal
  110312. functionality
  110313. synthetic
  110314. applications
  110315. water
  110316. soluble
  110317. acetate
  110318. pd/tppts
  110319. synthetic
  110320. developments
  110321. cycloreversion
  110322. synthetic
  110323. developments
  110324. cycloreversion
  110325. reactio
  110326. synthetic
  110327. methodology
  110328. using
  110329. organosulfur
  110330. compounds
  110331. synthetic
  110332. methods
  110333. strategies
  110334. total
  110335. synthesis
  110336. synthetic
  110337. methods
  110338. based
  110339. organozirconium
  110340. organocop
  110341. synthetic
  110342. methods
  110343. based
  110344. onium
  110345. salts
  110346. aza-arenes
  110347. synthetic
  110348. methods
  110349. lanthanides
  110350. synthetic
  110351. pathways
  110352. cyclobutanones
  110353. synthetic
  110354. reactions
  110355. based
  110356. onium
  110357. salts
  110358. synthetic
  110359. reactions
  110360. alkyl
  110361. carbonates
  110362. allyl
  110363. synthetic
  110364. transformations
  110365. organoboron
  110366. compounds
  110367. tailored
  110368. hosts
  110369. molecular
  110370. recognition
  110371. mechanical
  110372. tools
  110373. synthetic
  110374. organocopper
  110375. chemistry
  110376. total
  110377. syntheses
  110378. strychnine
  110379. transformations
  110380. 23-epoxy
  110381. alcohols
  110382. related
  110383. derivat
  110384. trends
  110385. dimetallic
  110386. synthons
  110387. trialkylsilyl
  110388. ether
  110389. chemistry
  110390. intramolecular
  110391. synthesis
  110392. oxoketene
  110393. acetals
  110394. types
  110395. metal
  110396. stabilized
  110397. cyclobutadiene
  110398. superphanes
  110399. usefu
  110400. reactions
  110401. novel
  110402. haloformates
  110403. related
  110404. reagen
  110405. sulfur
  110406. tetrafluoride
  110407. organic
  110408. synthesis
  110409. vistas
  110410. zeolite
  110411. molecular
  110412. sieve
  110413. catalysis
  110414. generating
  110415. organotin
  110416. reactive
  110417. intermediates
  110418. newall
  110419. newaz
  110420. newaz
  110421. recent
  110422. methods
  110423. synthesis
  110424. conjugated
  110425. newcomb
  110426. newcomb
  110427. martin
  110428. competition
  110429. methods
  110430. scales
  110431. alkyl
  110432. newcomb
  110433. martin
  110434. radical
  110435. kinetics
  110436. mechanistic
  110437. probe
  110438. studie
  110439. newer
  110440. newjersey
  110441. newkome
  110442. newkome
  110443. nayak
  110444. thiazolidinones
  110445. advances
  110446. newkome
  110447. george
  110448. moorefield
  110449. charles
  110450. baker
  110451. gregory
  110452. buildi
  110453. newkome
  110454. george
  110455. pyridylphosphines
  110456. chemical
  110457. reviews
  110458. newly
  110459. newman
  110460. newton
  110461. newton
  110462. marshall
  110463. quantum
  110464. chemical
  110465. probes
  110466. electron
  110467. transf
  110468. newton
  110469. roberts
  110470. steric
  110471. control
  110472. prostaglandin
  110473. synth
  110474. newyork
  110475. ngadjui
  110476. ngochindo
  110477. nguyen
  110478. mediated
  110479. coupling
  110480. reaction
  110481. asymmetric
  110482. process
  110483. mediated
  110484. intramolecular
  110485. cyclizations
  110486. enynes
  110487. niall
  110488. nibbering
  110489. nicholas
  110490. nicholas
  110491. nestle
  110492. seyferth
  110493. potential
  110494. utility
  110495. nicholson
  110496. nickel
  110497. element
  110498. application
  110499. industrial
  110500. homoge
  110501. nickel
  110502. element
  110503. applications
  110504. industrial
  110505. homog
  110506. nickel
  110507. palladium
  110508. catalysed
  110509. cross-coupling
  110510. reactions
  110511. nickel
  110512. catalysed
  110513. substitution
  110514. reactions
  110515. allylic
  110516. carbonate
  110517. nickel
  110518. mediated
  110519. cross-coupling
  110520. unactivated
  110521. neopentyl
  110522. nickel
  110523. mediated
  110524. intramolecular
  110525. cyclizations
  110526. eneyne
  110527. nickel
  110528. peroxide
  110529. oxidation
  110530. organic
  110531. compounds
  110532. nickel'ene
  110533. nickel-aluminium
  110534. nickel-aluminium
  110535. alloy
  110536. reducing
  110537. agent
  110538. nickel-catalysed
  110539. nickel-catalysed
  110540. nickel-catalyzed
  110541. nickel-catalyzed
  110542. cyclizations
  110543. alkynyl
  110544. enones
  110545. concomi
  110546. carbene
  110547. rearrangements
  110548. migra
  110549. nickson
  110550. nicola
  110551. nicolaidou
  110552. nicolaou
  110553. nicolaou
  110554. caulfield
  110555. groneberg
  110556. synthesis
  110557. novel
  110558. nicolaou
  110559. chemical
  110560. synthesis
  110561. glycosphingolipids
  110562. nicolaou
  110563. chemistry
  110564. biology
  110565. enediyne
  110566. antic
  110567. nicolaou
  110568. gasic
  110569. barnette
  110570. prostaglandin
  110571. endoperoxi
  110572. nicolaou
  110573. ogilvie
  110574. total
  110575. synthesis
  110576. amphoteronol
  110577. nicolaou
  110578. ramphal
  110579. petasis
  110580. serhan
  110581. lipoxins
  110582. nicolaou
  110583. battle
  110584. calicheamicin
  110585. angewandte
  110586. chemie
  110587. nicolaou
  110588. kyriacos
  110589. costa
  110590. rodney
  110591. kiplin
  110592. chemis
  110593. nicolaou
  110594. kyriacos
  110595. magic
  110596. enediyne
  110597. chemistry
  110598. chemistry
  110599. nicolas
  110600. nicole
  110601. nicolo
  110602. nicos
  110603. nicotianamine
  110604. nicotine
  110605. niecke
  110606. niecke
  110607. edgar
  110608. gudat
  110609. dietrich
  110610. iminophosphines
  110611. unconventional
  110612. nielsen
  110613. niemann
  110614. niessen
  110615. niessen
  110616. greef
  110617. liquid
  110618. chromatography
  110619. nieves
  110620. nifant'ev
  110621. nifant'ev
  110622. chemistry
  110623. phosphinylidene
  110624. compounds
  110625. advance
  110626. nifant'ev
  110627. predvoditelev
  110628. derivatives
  110629. trivalent
  110630. nigel
  110631. niitsuma
  110632. nikiforov
  110633. nikitina
  110634. nikkomycins
  110635. nikolai
  110636. nikolas
  110637. nikonov
  110638. nikonov
  110639. balyeva
  110640. compounds
  110641. containing
  110642. phosphorus
  110643. nikov
  110644. nimal
  110645. nine-membered
  110646. ninhydrin
  110647. ninhydrin
  110648. ninhydrin
  110649. analogs
  110650. syntheses
  110651. applications
  110652. ninomiya
  110653. ninomiya
  110654. naito
  110655. enamide
  110656. photocyclization
  110657. applicat
  110658. niobium
  110659. nippon
  110660. nippon
  110661. kagaku
  110662. kaishi
  110663. releasers
  110664. instant
  110665. color
  110666. nishibe
  110667. nishibe
  110668. bioactive
  110669. phenolic
  110670. compounds
  110671. traditional
  110672. medici
  110673. nishida
  110674. nishidu
  110675. nishigaichi
  110676. nishigaichi
  110677. yutaka
  110678. takuwa
  110679. naruta
  110680. yoshinori
  110681. maruyama
  110682. nishikawa
  110683. nishikubo
  110684. nishio
  110685. nishioka
  110686. nishiwaki
  110687. nishiwaki
  110688. recent
  110689. progress
  110690. chemistry
  110691. azaazu
  110692. nisms
  110693. nitramines
  110694. nitrate
  110695. nitrates
  110696. nitrating
  110697. nitration
  110698. methods
  110699. mechanisms
  110700. nitration
  110701. acetylsydnones
  110702. preparation
  110703. nitrations
  110704. nitratoiodination
  110705. nitrene
  110706. nitrene-induced
  110707. nitrenes
  110708. nitrenium
  110709. nitrenium
  110710. nitric
  110711. nitrilases
  110712. nitrile
  110713. nitrile
  110714. nitrile
  110715. imines
  110716. matrix
  110717. characterization
  110718. stable
  110719. compou
  110720. nitrile
  110721. oxide
  110722. complex
  110723. electrophilic
  110724. moiety
  110725. towards
  110726. nitrile
  110727. oxides
  110728. nitrile
  110729. oxides
  110730. nitrones
  110731. itronates
  110732. organic
  110733. chemistry
  110734. nitrile-stabilised
  110735. nitriles
  110736. nitrilimine
  110737. nitrilimines
  110738. nitrilium
  110739. nitrilium
  110740. salts
  110741. nitrite
  110742. nitrites
  110743. nitroM
  110744. nitro
  110745. nitro
  110746. compounds
  110747. nitro
  110748. compounds
  110749. recent
  110750. advances
  110751. syntheses
  110752. chemistry
  110753. nitro-compounds
  110754. nitro-derivatives
  110755. nitroacetic
  110756. nitroacetylamine
  110757. nitroacetylenes
  110758. nitroaldol
  110759. nitroaliphatic
  110760. nitroaliphatic
  110761. compounds
  110762. ideal
  110763. intermediates
  110764. organic
  110765. nitroalkanes
  110766. nitroalkanes
  110767. nitroalkenes
  110768. synthesis
  110769. nitroalkanols
  110770. nitroalkene
  110771. nitroalkene
  110772. cycloadditions
  110773. acyloxy
  110774. vinyl
  110775. ethers
  110776. nitroalkenesM
  110777. nitroalkenes
  110778. synthesis
  110779. heterocycles
  110780. nitroalkyl
  110781. nitroarenes
  110782. nitroaromatic
  110783. nitroaryl
  110784. nitroazaaromatics
  110785. nitroazines
  110786. nitroazoles
  110787. nitrobenzene
  110788. nitrobenzenesulfenat
  110789. nitrobicyclo
  110790. nitrocarboxylic
  110791. nitrochalcones
  110792. nitrocompounds
  110793. nitrocycloalkenes
  110794. nitrocyclohexanones
  110795. nitroenamines
  110796. nitroenamines
  110797. prepara
  110798. structure
  110799. synthetic
  110800. potential
  110801. nitroenamines
  110802. organic
  110803. synthesis
  110804. nitrogen
  110805. nitrogen
  110806. nitrogen
  110807. leaving
  110808. group
  110809. aliphatic
  110810. diazonium
  110811. nitrogen
  110812. donors
  110813. organometallic
  110814. chemistry
  110815. homogeneous
  110816. nitrogen
  110817. insertion
  110818. reaction
  110819. bridged
  110820. bicyclic
  110821. ketones
  110822. nitrogen
  110823. insertion
  110824. reactions
  110825. bridged
  110826. bicyclic
  110827. ketones
  110828. nitrogen
  110829. inversion
  110830. barrier
  110831. bicyclic
  110832. amines
  110833. energy
  110834. nitrogen
  110835. radicals
  110836. synthesis
  110837. intermediates
  110838. n-haloamide
  110839. nitrogen
  110840. stabilization
  110841. nitrogen
  110842. transfer
  110843. nitridomanganese
  110844. complex
  110845. aminatio
  110846. nitrogen
  110847. ylides
  110848. nitrogen-assisted
  110849. nitrogen-containing
  110850. nitrogen-heterocycli
  110851. nitrogen-stabilized
  110852. nitrogenase
  110853. nitrogenous
  110854. nitrogenous
  110855. natural
  110856. products
  110857. synthesis
  110858. n-acylnitroso
  110859. nitronates
  110860. nitrone
  110861. nitrone-olefin
  110862. nitrones
  110863. nitrones
  110864. nitrones
  110865. nitronates
  110866. nitroxides
  110867. nitronic
  110868. nitronic
  110869. acids
  110870. their
  110871. derivatives
  110872. nitronitriles
  110873. nitronium
  110874. nitroolefins
  110875. nitrophenyl
  110876. nitropyridine
  110877. nitrosamines
  110878. nitrosation
  110879. nitrosation
  110880. mechanisms
  110881. nitrosium
  110882. nitroso
  110883. nitroso
  110884. alkenes
  110885. nitroso
  110886. alkynes
  110887. nitroso-alkenes
  110888. nitroso-alkenes
  110889. nitroso-alkynes
  110890. nitroso-alkynes
  110891. nitrosoacetylamine
  110892. nitrosobenzene
  110893. nitrosodisulfonate
  110894. nitrosoimines
  110895. nitrosonium
  110896. nitrosyl
  110897. nitrotoluenes
  110898. nitrotrienes
  110899. nitrous
  110900. nitroxide
  110901. nitroxidesJ
  110902. nitroxyl
  110903. nitroxyl
  110904. radicals
  110905. nitroxides
  110906. nitta
  110907. nitta
  110908. makoto
  110909. reactions
  110910. vinylimino
  110911. phosphoranes
  110912. relate
  110913. nitya
  110914. nixon
  110915. nixon
  110916. fascinating
  110917. organometallic
  110918. chemistry
  110919. niyazymbetov
  110920. niyazymbetov
  110921. murat
  110922. evans
  110923. dennis
  110924. utility
  110925. carbanion
  110926. niyogi
  110927. nizar
  110928. chiral
  110929. solvating
  110930. agents
  110931. determ
  110932. nation
  110933. enantiomeric
  110934. purity
  110935. shift
  110936. reagents
  110937. olefins
  110938. aromatics
  110939. studies
  110940. three
  110941. types
  110942. highly
  110943. coordinates
  110944. organotin
  110945. noack
  110946. noarc
  110947. nobel
  110948. noble
  110949. noboru
  110950. nobujiro
  110951. nobumasa
  110952. nobuo
  110953. nocardicins
  110954. nodal
  110955. christian
  110956. bader
  110957. alfred
  110958. facts
  110959. better
  110960. dreams
  110961. noelle
  110962. noels
  110963. noels
  110964. graziani
  110965. hubert
  110966. catalysis
  110967. metal
  110968. compl
  110969. noeth
  110970. nogalamycin
  110971. nogarene
  110972. nohydrins
  110973. nojima
  110974. nojima
  110975. masatomo
  110976. chemistry
  110977. carbonyl
  110978. oxides
  110979. generated
  110980. nolan
  110981. determ
  110982. nation
  110983. enantiomeric
  110984. purity@
  110985. nolte@
  110986. nonan
  110987. nonhebel
  110988. derek
  110989. chemistry
  110990. cyclopropylmethyl
  110991. rela@
  110992. norgradi
  110993. stereochemistry
  110994. basic
  110995. concepts
  110996. applications
  110997. notermann
  110998. novel
  110999. novel
  111000. approach
  111001. lactams
  111002. triisopropylsilyl
  111003. azidohydrin
  111004. novel
  111005. benzoyl
  111006. migration
  111007. intermediary
  111008. adducts
  111009. novel
  111010. captodative
  111011. methylene
  111012. compounds
  111013. spontaneous
  111014. oxidation
  111015. organic
  111016. synthesis
  111017. wiley@
  111018. nucleopeptides@
  111019. nucleophilic
  111020. nucleophilic
  111021. coupling
  111022. radicals@
  111023. nucleosides@
  111024. o'connor
  111025. occurring
  111026. nolte
  111027. nomenclature
  111028. nomenclature
  111029. heterocyclic
  111030. compounds
  111031. nometallic
  111032. nomura
  111033. nomura
  111034. fukai
  111035. prenylflavonoids
  111036. non-aldol
  111037. non-aromatic
  111038. non-aromatics
  111039. non-bonding
  111040. non-bonding
  111041. molecular
  111042. orbitals
  111043. chemistry
  111044. non-clas
  111045. non-chelation
  111046. non-classical
  111047. non-enolizable
  111048. non-enzymatic
  111049. non-enzymatic
  111050. ymmetric
  111051. transformations
  111052. involving
  111053. symmetric
  111054. non-functionalizedH
  111055. non-heterocycles
  111056. non-metallic
  111057. non-natural
  111058. non-racemic
  111059. non-steroidal
  111060. non-transition
  111061. non-transition-metal
  111062. nonactate
  111063. nonalternant
  111064. nonan
  111065. nonan
  111066. nonane
  111067. nonanes
  111068. nonaromatic
  111069. nonbenzenoid
  111070. nonbiogenetic
  111071. nonbiomimetic
  111072. nonbonded
  111073. nonbridged
  111074. noncatalytic
  111075. noncatalytic
  111076. additions
  111077. alpha
  111078. beta-unsaturated
  111079. carbonyl
  111080. nonchair
  111081. nonchair
  111082. conformations
  111083. six-membered
  111084. rings
  111085. nonclassical
  111086. nonconcerted
  111087. nonconcerted
  111088. paths
  111089. reactions
  111090. alkene
  111091. zirconocene
  111092. compl
  111093. nonconjugated
  111094. nonconventional
  111095. nonconventional
  111096. reaction
  111097. conditions
  111098. ultrasound
  111099. pressure
  111100. noncovalent
  111101. noncovalent
  111102. design
  111103. principles
  111104. synthesis
  111105. noncyclic
  111106. nonenzymic
  111107. nones
  111108. nonfunctionalized
  111109. nonhebel
  111110. nonhebel
  111111. tedder
  111112. walton
  111113. radicals
  111114. cambridge
  111115. univer
  111116. nonhebel
  111117. derek
  111118. chemistry
  111119. cyclopropylmethyl
  111120. nonlinear
  111121. nonlinear
  111122. effects
  111123. asymmetric
  111124. catalysis
  111125. nonmacrocyclic
  111126. nonmolecular
  111127. nonperfect
  111128. nonplanar
  111129. nonproteinogenic
  111130. nonprotonated
  111131. nonracemic
  111132. nonracernic
  111133. nonradical
  111134. nonrigid
  111135. nonstabilised
  111136. nonstabilised
  111137. azomethine
  111138. ylides
  111139. nonstabilized
  111140. nonstandard
  111141. nonstereogenic
  111142. nonstereospecific
  111143. nonstereospecific
  111144. mechanisms
  111145. asymmetric
  111146. addition
  111147. alken
  111148. nonterpenoids
  111149. nontraditional
  111150. nontransition
  111151. noordik
  111152. norbert
  111153. norbornadiene
  111154. norbornadienes
  111155. norbornene
  111156. norbornenylidenes
  111157. norbornyl
  111158. norbornylogous
  111159. nordahl
  111160. norephedrine
  111161. noresquiterpene
  111162. norgradi
  111163. norgradi
  111164. stereochemistry
  111165. basic
  111166. concepts
  111167. applications
  111168. norihiko
  111169. norin
  111170. norma
  111171. normal
  111172. normal-arylmaleimide
  111173. normanv
  111174. norman
  111175. applications
  111176. spectroscopy
  111177. kinetics
  111178. norman
  111179. principles
  111180. organic
  111181. synthesis
  111182. halsted
  111183. norman
  111184. principles
  111185. organic
  111186. synthesis
  111187. wiley
  111188. norman
  111189. richard
  111190. coxon
  111191. james
  111192. principles
  111193. organic
  111194. synth
  111195. normant
  111196. normant
  111197. alexakis
  111198. metallation
  111199. alkynes
  111200. stereospecif
  111201. normant
  111202. marek
  111203. ilane
  111204. lefrancois
  111205. michel
  111206. organobis
  111207. norris
  111208. norrish
  111209. norrish
  111210. photocleavage
  111211. azabicyclo
  111212. 3.3.1
  111213. nonan
  111214. norrix
  111215. norsteroid
  111216. north
  111217. north
  111218. michael
  111219. catalytic
  111220. asymmetric
  111221. cyanohydrin
  111222. synthesis
  111223. norton
  111224. noselenium
  111225. notario
  111226. notation
  111227. notermann
  111228. notermann
  111229. notesR
  111230. novak
  111231. novel
  111232. novel
  111233. novel
  111234. amidoalkylation
  111235. 4-acetoxyazeidinones
  111236. allylic
  111237. novel
  111238. facile
  111239. reduction
  111240. phenol
  111241. derivatives
  111242. samari
  111243. novel
  111244. application
  111245. radical
  111246. reactions
  111247. preparative
  111248. novel
  111249. applications
  111250. vinylogous
  111251. mannich
  111252. reactions
  111253. total
  111254. novel
  111255. approach
  111256. chrysanthemic
  111257. acids
  111258. novel
  111259. aspects
  111260. eta'-diiod
  111261. coordination
  111262. diiodine
  111263. novel
  111264. asymmetric
  111265. synthesis
  111266. g-alkylated
  111267. lactones
  111268. succe
  111269. novel
  111270. benzoyl
  111271. migration
  111272. intermediary
  111273. adducts
  111274. novel
  111275. blue-transperent
  111276. frequency
  111277. doublers
  111278. based
  111279. 18-di
  111280. novel
  111281. carbohydrate
  111282. transformations
  111283. discovered
  111284. route
  111285. novel
  111286. carbon
  111287. compounds
  111288. naked
  111289. units
  111290. novel
  111291. catalytic
  111292. cycle
  111293. synthesis
  111294. epoxides
  111295. novel
  111296. catalytic
  111297. effect
  111298. reduction
  111299. novel
  111300. concepts
  111301. directed
  111302. biaryl
  111303. synthesis
  111304. approac
  111305. novel
  111306. conversion
  111307. stereoselectivity
  111308. stereoselectivi
  111309. novel
  111310. conversion
  111311. epoxides
  111312. carbon
  111313. homologated
  111314. allyl
  111315. novel
  111316. cyclization
  111317. reaction
  111318. tandem
  111319. michael
  111320. addition
  111321. dieckm
  111322. novel
  111323. dialkyl
  111324. halotetrafluoroethyl
  111325. phosphonates
  111326. facile
  111327. novel
  111328. gabriel
  111329. reagents
  111330. novel
  111331. general
  111332. route
  111333. synthesis
  111334. carboxylic
  111335. novel
  111336. generation
  111337. arylsulfenium
  111338. intermediates
  111339. novel
  111340. insertion
  111341. rearrangement
  111342. addition
  111343. products
  111344. novel
  111345. intramolecular
  111346. reactions
  111347. allenylsilanes
  111348. novel
  111349. lewis
  111350. catalysis
  111351. organic
  111352. synthesis
  111353. novel
  111354. light
  111355. emitting
  111356. reaction
  111357. 2-phenylsulfonyl
  111358. 3-phenyl
  111359. novel
  111360. michael
  111361. additions
  111362. phenols
  111363. promoted
  111364. osmium
  111365. novel
  111366. quinodimethane
  111367. tandem
  111368. diels
  111369. alder
  111370. reaction
  111371. novel
  111372. organic
  111373. peroxygen
  111374. reagents
  111375. organic
  111376. synthesi
  111377. novel
  111378. organic
  111379. synthesis
  111380. catalysed
  111381. novel
  111382. oxidative
  111383. conversion
  111384. unsaturated
  111385. acids
  111386. novel
  111387. palladium
  111388. catalyzed
  111389. cyclization
  111390. aziridines
  111391. novel
  111392. peric
  111393. reactions
  111394. perimeter
  111395. chemistry
  111396. novel
  111397. polyhydroxylated
  111398. quinolizidines
  111399. expanded
  111400. analogs
  111401. novel
  111402. porphyrinoids
  111403. novel
  111404. potentially
  111405. useful
  111406. spin-label
  111407. reagents
  111408. novel
  111409. pyridodiindoles
  111410. azadiindoles
  111411. indolopyridoimidazol
  111412. novel
  111413. radical
  111414. cyclizations
  111415. alkyl
  111416. azides
  111417. route
  111418. novel
  111419. reactivity
  111420. stabilized
  111421. methylenetributylpho
  111422. novel
  111423. opening
  111424. reaction
  111425. chromanone
  111426. oxime
  111427. novel
  111428. route
  111429. fused
  111430. nitrogen
  111431. heterocycles
  111432. olefin
  111433. metathe
  111434. novel
  111435. serotonin-3
  111436. receptor
  111437. antagonists
  111438. novel
  111439. stereoselective
  111440. cylization
  111441. p-allylnickel
  111442. complex
  111443. novel
  111444. structure
  111445. elucidation
  111446. toxin
  111447. backbone
  111448. novel
  111449. synthesis
  111450. cyclopropylaminosulf
  111451. salts
  111452. dimethyla
  111453. novel
  111454. synthesis
  111455. dienylsiloxanes
  111456. stereoselective
  111457. synthesis
  111458. novel
  111459. synthesis
  111460. heterocycles
  111461. using
  111462. zirconium
  111463. catalyzed
  111464. novel
  111465. synthetic
  111466. approaches
  111467. intensely
  111468. sweet
  111469. gylcosides
  111470. novel
  111471. tandem
  111472. cyclization
  111473. oxidation
  111474. reaction
  111475. allenyl
  111476. hydra
  111477. novel
  111478. umpolung
  111479. formation
  111480. catalyzed
  111481. triphenyl
  111482. novelty
  111483. novikov
  111484. novikova
  111485. novotny
  111486. nowick
  111487. nowlan
  111488. nowotny
  111489. noyori
  111490. noyori
  111491. organic
  111492. synthesis
  111493. japan
  111494. present
  111495. future
  111496. noyori
  111497. ryoji
  111498. asymmetric
  111499. catalysis
  111500. organic
  111501. synthesis
  111502. wiley
  111503. noyori
  111504. ryoji
  111505. organometallic
  111506. multiplication
  111507. nozaki
  111508. nozaki
  111509. hitosi
  111510. metals
  111511. carbene
  111512. synthon
  111513. introduc
  111514. nozaki-hiyama
  111515. nozaki-hiyama-kishi
  111516. seventy
  111517. years
  111518. organic
  111519. chemistry
  111520. profiles
  111521. npropylammonium
  111522. nsertions
  111523. nsions
  111524. nthesis
  111525. ntred
  111526. nubar
  111527. nucieic
  111528. nuclear
  111529. nuclei
  111530. nucleic
  111531. nucleic
  111532. chemistry
  111533. improved
  111534. synthetic
  111535. proce
  111536. nucleic
  111537. acids
  111538. chemistry
  111539. biology
  111540. nucleoaminoacids
  111541. nucleofugal
  111542. nucleofugality
  111543. nucleopeptides
  111544. nucleophiiic
  111545. nucleophiiic
  111546. substitution
  111547. hydrogen
  111548. azines
  111549. nucleophile
  111550. nucleophiles
  111551. nucleophiles
  111552. allyl-metal
  111553. complexes
  111554. nucleophiles
  111555. cationic
  111556. pentadienyl-metal
  111557. complexes
  111558. nucleophilicq
  111559. nucleophilic
  111560. nucleophilic
  111561. addition
  111562. reactions
  111563. cationic
  111564. alkyne
  111565. nucleophilic
  111566. addition
  111567. arene-metal
  111568. complexes
  111569. nucleophilic
  111570. addition
  111571. carboxylic
  111572. derivatives
  111573. nucleophilic
  111574. addition
  111575. diene
  111576. arene-metal
  111577. complexes
  111578. nucleophilic
  111579. addition
  111580. imines
  111581. imine
  111582. derivatives
  111583. nucleophilic
  111584. addition
  111585. olefins
  111586. kinetics
  111587. mechanism
  111588. nucleophilic
  111589. addition-electrophil
  111590. coupling
  111591. carbanion
  111592. nucleophilic
  111593. additions
  111594. organotransition
  111595. metal
  111596. cations
  111597. nucleophilic
  111598. additions
  111599. pyridinium
  111600. salts
  111601. reduction
  111602. nucleophilic
  111603. electrophilic
  111604. catalysis
  111605. transition
  111606. nucleophilic
  111607. organometall
  111608. displacement
  111609. reactions
  111610. nucleophilic
  111611. aromatic
  111612. displacement
  111613. influence
  111614. nucleophilic
  111615. coupling
  111616. radicals
  111617. nucleophilic
  111618. coupling
  111619. arynes
  111620. nucleophilic
  111621. displacement
  111622. recent
  111623. developments
  111624. nucleophilic
  111625. displacement
  111626. aromatic
  111627. nitro
  111628. groups
  111629. nucleophilic
  111630. eliminative
  111631. fission
  111632. nucleophilic
  111633. perfluoroalkylation
  111634. using
  111635. perfluoroalkyllithiu
  111636. nucleophilic
  111637. reactions
  111638. acetals
  111639. alkyl
  111640. sulfonates
  111641. oxira
  111642. nucleophilic
  111643. reactions
  111644. quinones
  111645. nucleophilic
  111646. opening
  111647. tetrahydro
  111648. oxazines
  111649. nucleophilic
  111650. substitution
  111651. saturated
  111652. carbon
  111653. atoms
  111654. mechanis
  111655. nucleophilic
  111656. substitution
  111657. mechanism
  111658. alkyl
  111659. nucleophilic
  111660. vinylic
  111661. substitution
  111662. nucleophilic
  111663. vinylic
  111664. substitution
  111665. single
  111666. multistep
  111667. nucleophilic-substit
  111668. nucleophilicity
  111669. nucleoside
  111670. nucleoside
  111671. synthesis
  111672. organosilic
  111673. methods
  111674. nucleosidesp
  111675. nucleoti
  111676. nucleotide
  111677. nucleotides
  111678. nucleus
  111679. nud'ga
  111680. nudelman
  111681. nudelman
  111682. chemistry
  111683. optically
  111684. active
  111685. sulfur
  111686. compound
  111687. nugent
  111688. nugent
  111689. william
  111690. rajanbabu
  111691. beyond
  111692. nature's
  111693. numata
  111694. number
  111695. numbers
  111696. nuphar
  111697. nupharamine
  111698. nuphenine
  111699. nuria
  111700. nurmukhametov
  111701. nurrenbach
  111702. nussbeutel
  111703. nutaitis
  111704. nutley
  111705. chemical
  111706. philosophy
  111707. theoretical
  111708. chemistr
  111709. nyiredy
  111710. ttanasi
  111711. caglioti
  111712. proced
  111713. gansow
  111714. vernon
  111715. carbon
  111716. studies
  111717. organomet
  111718. exner
  111719. dipole
  111720. moments
  111721. configurations
  111722. conformations
  111723. gano-transition
  111724. metal
  111725. compounds
  111726. containing
  111727. perfluorinated
  111728. hofer
  111729. lanthanide
  111730. induced
  111731. shift
  111732. technique
  111733. applications
  111734. hydroxyaryl
  111735. ketones
  111736. organic
  111737. synthesis
  111738. hydroxyaryl
  111739. ketones
  111740. organic
  111741. synthesis
  111742. review
  111743. chupakhin
  111744. postovskii
  111745. silylated
  111746. enolates
  111747. versatile
  111748. intermediates
  111749. organic
  111750. strouf
  111751. casensky
  111752. kubanek
  111753. sodium
  111754. dihydro
  111755. metho
  111756. o'brien
  111757. o'brien
  111758. nuclear
  111759. magnetic
  111760. resonance
  111761. carbanions
  111762. o'connor
  111763. o'connor
  111764. o'donnellt
  111765. o'donnell
  111766. huffman
  111767. active
  111768. catalyst
  111769. specit
  111770. o'hagan
  111771. o'hagan
  111772. biosynthesis
  111773. fatty
  111774. polyketide
  111775. metaboli
  111776. o'hagan
  111777. david
  111778. biosynthesis
  111779. polyketide
  111780. metabolites
  111781. o'hagan
  111782. david
  111783. polyketide
  111784. metabolites
  111785. ellis
  111786. horwood
  111787. o'hare
  111788. o'hare
  111789. structure
  111790. dynamics
  111791. electronic
  111792. properties
  111793. o'neil
  111794. o-acyl
  111795. o-acyl
  111796. thiohydroxamates
  111797. versatile
  111798. sources
  111799. alkyl
  111800. o-antigens
  111801. o-bis
  111802. o-bond
  111803. o-c-n
  111804. o-carbamate
  111805. o-displacement
  111806. o-esters
  111807. o-glycosylation
  111808. o-hydroxyaryl
  111809. o-hydroxyaryl
  111810. ketones
  111811. organic
  111812. synthesis
  111813. o-mesitylenesul
  111814. o-mesitylenesul
  111815. onylhydroxylamine
  111816. related
  111817. compounds
  111818. o-methyl
  111819. o-methyl-n9-desmethy
  111820. o-methylbouvardin
  111821. o-quinodimet
  111822. o-quinodimethanes
  111823. o-quinones
  111824. o-quinonoid
  111825. o-silyl
  111826. o-silylated
  111827. o-silylated
  111828. enolates
  111829. versatile
  111830. intermediates
  111831. organic
  111832. o-stannyl
  111833. o-substituted
  111834. o-xylylenes
  111835. o/n-acetals
  111836. o/n-acetals
  111837. cyclic
  111838. structure
  111839. o/n-acetals
  111840. cyclic
  111841. structure
  111842. o/n-acetals
  111843. cyclic
  111844. o-c-n
  111845. structure
  111846. o/o-acetals
  111847. o/o-acetals
  111848. general
  111849. o/o-acetals
  111850. duction
  111851. o/o-acetals
  111852. special
  111853. oh/oh-acetals
  111854. lactols
  111855. 135-trioxanes
  111856. o/s-acetals
  111857. numata
  111858. pummerer
  111859. pummerer
  111860. reactions
  111861. shigeru
  111862. joyce
  111863. organic
  111864. sulfur
  111865. chemistry
  111866. struc
  111867. shigeru
  111868. small
  111869. compounds
  111870. containing
  111871. sulfur
  111872. atoms
  111873. shigeru
  111874. uchida
  111875. yuzuru
  111876. ligand
  111877. coupling
  111878. reactions
  111879. hyper
  111880. obafluorin
  111881. oberg
  111882. oberhauser
  111883. obraztsov
  111884. observation
  111885. observation
  111886. catalytic
  111887. intermediates
  111888. suzuki
  111889. reactio
  111890. observations
  111891. observations
  111892. chemistry
  111893. biology
  111894. cyclic
  111895. enediyne
  111896. obtainable
  111897. obtained
  111898. obtaining
  111899. ocams
  111900. occolowitz
  111901. occurrence
  111902. occurring
  111903. occurring
  111904. ochiai
  111905. ochoa
  111906. octa-26-diene
  111907. octadienes
  111908. octahydrohistrionico
  111909. octalactin
  111910. octan
  111911. octane
  111912. octanes
  111913. octatetraene
  111914. octatetrayne
  111915. octenes
  111916. octenones
  111917. octopus
  111918. octulosonic
  111919. odashima
  111920. odette
  111921. odinokov
  111922. odinokov
  111923. kukovinets
  111924. zainullin
  111925. tolstikov
  111926. odysseym
  111927. oene/oene-acetals
  111928. oesterle
  111929. ogura
  111930. haruo
  111931. hasegawa
  111932. akira
  111933. suami
  111934. tetsuo
  111935. carbohydrates
  111936. hiromichi
  111937. microbial
  111938. oxidation
  111939. organic
  111940. sulfur
  111941. compoun@
  111942. olefin
  111943. olefin
  111944. cyclisation
  111945. processes
  111946. carbon-carbon
  111947. bonds@
  111948. olefins
  111949. olefins
  111950. amines
  111951. hofmann
  111952. elimination
  111953. reaction
  111954. oligomerizations@
  111955. olofson@
  111956. quantifying
  111957. chirality@
  111958. heterocycles
  111959. synthetic
  111960. opportunities@
  111961. optically
  111962. 7-oxabicyclo
  111963. 2.2.1
  111964. hept-5-en-2-yl
  111965. derivatives@
  111966. or/oene-acetals@
  111967. orena
  111968. organic
  111969. organic
  111970. pressure
  111971. chemistry
  111972. studies
  111973. organic
  111974. chemistry@
  111975. organic
  111976. reactivity
  111977. control
  111978. means
  111979. neighboring
  111980. groups
  111981. organic
  111982. synthesis
  111983. carbonylation
  111984. organometallic
  111985. reagen@
  111986. organo
  111987. ogura
  111988. haruo
  111989. hasegawa
  111990. akira
  111991. suami
  111992. tetsuo
  111993. carbohydrates
  111994. ogura
  111995. katsuyuki
  111996. combination
  111997. group
  111998. taeboem
  111999. reilly
  112000. michael
  112001. reagent
  112002. controlled
  112003. asymmetric
  112004. acetals
  112005. linear
  112006. o-c-n
  112007. structure
  112008. oh/oh-acetals
  112009. ohanessian
  112010. ohare
  112011. ohare
  112012. organic
  112013. organometallic
  112014. guests
  112015. intercalated
  112016. ohashi
  112017. ohashi
  112018. reactivity
  112019. molecular
  112020. crystals
  112021. kodansha
  112022. tokyo
  112023. ohfune
  112024. ohfune
  112025. yasufumi
  112026. stereoselective
  112027. routes
  112028. toward
  112029. synthesis
  112030. ohioff
  112031. ohioff
  112032. recent
  112033. developments
  112034. field
  112035. naturally
  112036. occur
  112037. ohler
  112038. ohlmeyer
  112039. ohloff
  112040. ohloff
  112041. flament
  112042. heteroatomic
  112043. substances
  112044. aroma
  112045. compound
  112046. ohloff
  112047. guther
  112048. scent
  112049. fragrances
  112050. translation
  112051. riechstoff
  112052. ohmaye
  112053. ohmoto
  112054. ohshiro
  112055. hiromichi
  112056. microbial
  112057. oxidation
  112058. organic
  112059. sulfur
  112060. compoun
  112061. ohtsuka
  112062. ohuchi
  112063. oi-pr
  112064. oishi
  112065. oishi
  112066. takeshi
  112067. nakata
  112068. tadashi
  112069. aspects
  112070. stereoselective
  112071. ojima
  112072. applications
  112073. thionyl
  112074. chloride
  112075. synthetic
  112076. okabe
  112077. okafor
  112078. okafor
  112079. chemistry
  112080. biological
  112081. activity
  112082. azapheno
  112083. okamoto
  112084. okamoto
  112085. yoshiki
  112086. takamuku
  112087. setsuo
  112088. photochemical
  112089. cleav
  112090. okamura
  112091. okamura
  112092. william
  112093. curtin
  112094. michael
  112095. pericyclization
  112096. vinyla
  112097. okano
  112098. okazaki
  112099. okhlobystin
  112100. michinori
  112101. chemistry
  112102. rotational
  112103. isomers
  112104. reactivity
  112105. okita
  112106. okitsu
  112107. okubo
  112108. okubo
  112109. masao
  112110. matsuo
  112111. reagents
  112112. variety
  112113. reaction
  112114. okuda
  112115. okuda
  112116. yoshida
  112117. hatano
  112118. tannins
  112119. medicinal
  112120. plant
  112121. okuyama
  112122. boron
  112123. trifluoride
  112124. antimony
  112125. pentafluoride
  112126. synthetic
  112127. reagents
  112128. reactions
  112129. parker
  112130. yoneda
  112131. superacid
  112132. catalyzed
  112133. oxygenation
  112134. synthetic
  112135. reagents
  112136. reactions
  112137. george
  112138. prakash
  112139. surya
  112140. chambers
  112141. richard
  112142. synth
  112143. george
  112144. reddy
  112145. prakash
  112146. prakash
  112147. surya
  112148. lived
  112149. george
  112150. squire
  112151. david
  112152. chemistry
  112153. energetic
  112154. material
  112155. olate
  112156. olates
  112157. older
  112158. oldham
  112159. oleandomycin
  112160. oleanolic
  112161. oleate
  112162. olefin
  112163. olefin
  112164. esses
  112165. carbon-carbon
  112166. bonds
  112167. olefin
  112168. cyclisation
  112169. processes
  112170. carbon-heteroatom
  112171. olefin
  112172. inversion
  112173. olefin
  112174. inversion
  112175. isomers
  112176. olefin
  112177. synthesis
  112178. deoxygenation
  112179. vicinal
  112180. diols
  112181. olefin
  112182. synthesis
  112183. organometallic
  112184. coupling
  112185. reactions
  112186. olefin
  112187. synthesis
  112188. organic
  112189. phosphonate
  112190. carbanions
  112191. olefin-forming
  112192. olefination
  112193. olefinic
  112194. olefinic
  112195. microbial
  112196. metabolites
  112197. excluding
  112198. macrocyclic
  112199. compoun
  112200. olefinsG
  112201. olefins
  112202. hofmann
  112203. elimination
  112204. reaction
  112205. oleinik
  112206. olekhnovich
  112207. olfactory
  112208. oligo
  112209. oligodeoxyguanylates
  112210. oligodeoxyguanylates
  112211. self-assembly
  112212. leading
  112213. oligodeoxyribonucleo
  112214. oligoethers
  112215. oligoglycosides
  112216. oligomeric
  112217. oligomerisation
  112218. oligomerization
  112219. oligomerizations
  112220. oligomers
  112221. oligon
  112222. oligonucleotide
  112223. oligonucleotides
  112224. oligonucleotides
  112225. analogs
  112226. practical
  112227. approach
  112228. oligopeptide
  112229. oligopyridines
  112230. oligopyridines
  112231. helicating
  112232. ligands
  112233. oligopyrroles
  112234. oligoribonucleotide
  112235. oligoribonucleotides
  112236. oligosaccharide
  112237. oligosaccharides
  112238. oligosaccharidesnare
  112239. oligosaccharins
  112240. oligosaccharins
  112241. class
  112242. signal
  112243. oligosaccharins
  112244. class
  112245. signalling
  112246. molecules
  112247. plant
  112248. oligosacharide
  112249. olive
  112250. oliveira
  112251. oliver
  112252. olivera
  112253. olivero
  112254. oliveros
  112255. olivier
  112256. olivo
  112257. olivomycin
  112258. olivucci
  112259. oller
  112260. olofson
  112261. ologies}
  112262. olsen
  112263. olsson
  112264. organometallic
  112265. intramolecular
  112266. coordination
  112267. compounds
  112268. omega
  112269. omega-alkanediols
  112270. omega-aminoalkylhete
  112271. omega-aminoalkylhete
  112272. actual
  112273. aspects
  112274. chemistry
  112275. ometallics
  112276. omolecular
  112277. ompounds
  112278. omran
  112279. structure
  112280. organometal
  112281. complexes
  112282. conformation
  112283. lactone
  112284. rings
  112285. diastereoselectivity
  112286. cyanide
  112287. addition
  112288. hydroxy
  112289. formation
  112290. sulfonylamino
  112291. sulfonyl
  112292. isocyanates
  112293. influence
  112294. heteroatoms
  112295. alpha-and
  112296. beta-functional
  112297. influence
  112298. spiroconjugation
  112299. electron
  112300. withdrawin
  112301. mechanism
  112302. asymmetric
  112303. dihydroxylation
  112304. alkenes
  112305. mechanism
  112306. formation
  112307. pyrazoles
  112308. diketones
  112309. nature
  112310. asymmetric
  112311. induction
  112312. palladium
  112313. nature
  112314. electronic
  112315. interaction
  112316. between
  112317. conjugat
  112318. orgin
  112319. enantioselectivity
  112320. dihydroxylati
  112321. question
  112322. symmetry
  112323. formally
  112324. symmetrical
  112325. reaction
  112326. dichloro
  112327. azoniaallene
  112328. salts
  112329. mechanistic
  112330. possibilities
  112331. stereochemical
  112332. outcome
  112333. mcmurry
  112334. coupling
  112335. stereochemistry
  112336. nucleophilic
  112337. additions
  112338. tetrahyd
  112339. stereochemistry
  112340. photoaddition
  112341. between
  112342. unsaturated
  112343. synthesis
  112344. pyrido
  112345. 321-kl
  112346. phenothiazine
  112347. quino
  112348. 81-bc
  112349. trail
  112350. metathesis
  112351. catalysts
  112352. symmetric
  112353. aziridines
  112354. chiral
  112355. auxiliaries
  112356. utility
  112357. heteroatom
  112358. substituted
  112359. ortho
  112360. esters
  112361. onaka
  112362. carbon
  112363. expansions
  112364. bridged
  112365. bicyclic
  112366. ketones
  112367. century
  112368. physical
  112369. organic
  112370. chemistry
  112371. menshutkin
  112372. electron
  112373. electron
  112374. change
  112375. hundred
  112376. years
  112377. sulfenic
  112378. chemistry
  112379. oxidation
  112380. hundred
  112381. years
  112382. sulfenic
  112383. chemistry
  112384. substitutio
  112385. preparation
  112386. chiral
  112387. vinyl
  112388. benzodioxane
  112389. synthesis
  112390. unsaturated
  112391. ketones
  112392. butyl
  112393. synthesis
  112394. ethyl
  112395. hydroxyalkyl
  112396. aminoalkanoates
  112397. synthesis
  112398. haloacetylenes
  112399. trimethylsilyl
  112400. synthesis
  112401. homoallylic
  112402. alcohols
  112403. dienes
  112404. chromium
  112405. mediated
  112406. homologation
  112407. aldehydes
  112408. conversion
  112409. esters
  112410. azides
  112411. using
  112412. diethylal
  112413. functionalization
  112414. dioxaspirodecanes
  112415. b-pheny
  112416. substitutive
  112417. acyloxylation
  112418. carbon
  112419. reactio
  112420. synthesis
  112421. amino
  112422. methylimidazo
  112423. quinoline
  112424. one-carbon
  112425. one-carbon-homologat
  112426. transfer
  112427. reactions
  112428. pyrylium
  112429. cations
  112430. one-half
  112431. one-pot
  112432. one-pot
  112433. synthesis
  112434. 2-alkyltetrahydropyr
  112435. 3-nitro-56-di
  112436. one-step
  112437. one-way
  112438. onion
  112439. onium
  112440. transformations
  112441. heterocycles
  112442. synthetic
  112443. onoue
  112444. onylhydroxylamine
  112445. oosthuizen
  112446. opallo
  112447. open-chain
  112448. open-chain
  112449. polyphosphorus
  112450. hydrides
  112451. phosphanes
  112452. opening
  112453. aziridines
  112454. methylindole
  112455. regioselectivity
  112456. openings
  112457. operate
  112458. operational
  112459. operationally
  112460. opinions
  112461. opioid
  112462. opium
  112463. opment
  112464. oppenaner
  112465. oppenauer
  112466. oppenauer-type
  112467. oppolzer
  112468. oppolzer
  112469. intramolecular
  112470. cycloaddition
  112471. reactions
  112472. ortho
  112473. oppolzer
  112474. snieckus
  112475. intramolecular
  112476. reactions
  112477. organi
  112478. oppolzer's
  112479. opportunities
  112480. opportunities
  112481. asymmetric
  112482. synthesis
  112483. industrial
  112484. prospect
  112485. opportunity
  112486. opposite
  112487. optic
  112488. optical
  112489. optically
  112490. synthesis
  112491. artificial
  112492. transami
  112493. optically
  112494. active
  112495. chiral
  112496. polymers
  112497. optically
  112498. active
  112499. cyclopropanes
  112500. optically
  112501. active
  112502. n-protected
  112503. alpha-amino
  112504. aldehydes
  112505. organi
  112506. optically
  112507. active
  112508. ruthenocenylbis
  112509. phosphines
  112510. effieient
  112511. optically
  112512. 7-oxabicyclo
  112513. 2.2.1
  112514. hept-5-en-2-yl
  112515. derivatives
  112516. optimisation
  112517. optimization
  112518. optimization
  112519. enantiocontrol
  112520. carbon-hydrogen
  112521. insertion
  112522. or/n-acetals
  112523. or/n-acetals
  112524. linear
  112525. o-c-n
  112526. structure
  112527. or/oene-acetals
  112528. oragnic
  112529. orally
  112530. cuprate
  112531. orbital
  112532. orbital
  112533. interaction
  112534. theory
  112535. organic
  112536. chemistry
  112537. orbital
  112538. interaction
  112539. through
  112540. space
  112541. through
  112542. bonds
  112543. orbital
  112544. interaction
  112545. through
  112546. space
  112547. through
  112548. sigma-bonds
  112549. orbital
  112550. interactions
  112551. chemistry
  112552. orbitals
  112553. orbitals
  112554. distortion
  112555. carbonyl
  112556. olefin
  112557. groups
  112558. unsymmetri
  112559. orchin
  112560. orchin
  112561. quintessential
  112562. catalyst
  112563. orchin
  112564. kaplan
  112565. macomber
  112566. wilson
  112567. zimmer
  112568. orderK
  112569. ordering
  112570. orders
  112571. ordination
  112572. orekhov
  112573. orena
  112574. orena
  112575. oreste
  112576. functional
  112577. group
  112578. preparations
  112579. procedure
  112580. synthesis
  112581. alpha
  112582. aminoald
  112583. orgamic
  112584. organ
  112585. organc
  112586. organicK
  112587. organic
  112588. organic
  112589. organic
  112590. organic
  112591. organic
  112592. organic
  112593. organic
  112594. organic
  112595. organic
  112596. organic
  112597. organic
  112598. clays
  112599. organic
  112600. chemistry
  112601. unconventional
  112602. solvents
  112603. organic
  112604. chemistry
  112605. lactams
  112606. organic
  112607. chemistry
  112608. low-valent
  112609. titanium
  112610. organic
  112611. chemistry
  112612. lanthanides
  112613. organic
  112614. compounds
  112615. alkali
  112616. metals
  112617. organic
  112618. derivatives
  112619. manganese
  112620. organic
  112621. synthesis
  112622. organic
  112623. derivatives
  112624. sulfurous
  112625. organic
  112626. diazonium
  112627. compounds
  112628. organic
  112629. dications
  112630. gas-phase
  112631. experiments
  112632. theory
  112633. concer
  112634. organic
  112635. diradicals
  112636. polyradicals
  112637. coupling
  112638. organic
  112639. electrochemistry
  112640. introduction
  112641. guide
  112642. organic
  112643. halides
  112644. organic
  112645. pressure
  112646. chemistry
  112647. organic
  112648. pressure
  112649. chemistry
  112650. studies
  112651. organic
  112652. chemistry
  112653. organic
  112654. hydrazines
  112655. organic
  112656. hydrazinium
  112657. compounds
  112658. organic
  112659. hydroxylamines
  112660. organic
  112661. pairs
  112662. intermediates
  112663. nucleophilic
  112664. substitut
  112665. organic
  112666. nitrates
  112667. organic
  112668. nitrites
  112669. carboxylic
  112670. nitrous
  112671. anhydrides
  112672. organic
  112673. nitrosonium
  112674. salts
  112675. oxidants
  112676. organic
  112677. chemistry
  112678. organic
  112679. photochemistry
  112680. organic
  112681. photochemistry
  112682. comprehensive
  112683. treatment
  112684. organic
  112685. photochemistry
  112686. visual
  112687. approach
  112688. organic
  112689. photochemistry
  112690. organized
  112691. media
  112692. organic
  112693. photochemistry
  112694. principles
  112695. applications
  112696. organic
  112697. photochromes
  112698. organic
  112699. radical
  112700. cations
  112701. fluid
  112702. solution
  112703. unusual
  112704. structures
  112705. organic
  112706. radical
  112707. rigid
  112708. systems
  112709. organic
  112710. reaction
  112711. carbon
  112712. disulfide
  112713. overall
  112714. review
  112715. organic
  112716. reactions
  112717. aqueous
  112718. media
  112719. focus
  112720. carbon-ca
  112721. organic
  112722. reactions
  112723. carbon
  112724. disulfide
  112725. organic
  112726. reactions
  112727. selected
  112728. complexes
  112729. annual
  112730. survey
  112731. organic
  112732. reactivity
  112733. control
  112734. means
  112735. neighboring
  112736. groups
  112737. organic
  112738. selenium
  112739. tellurium
  112740. compounds
  112741. organic
  112742. sulfur
  112743. compounds
  112744. organic
  112745. synthesis
  112746. recent
  112747. organic
  112748. sulfuranyl
  112749. radicals
  112750. organic
  112751. hesis
  112752. alpha-chlorosulfides
  112753. organic
  112754. syntheses
  112755. based
  112756. reactions
  112757. unnamed
  112758. reacti
  112759. organic
  112760. syntheses
  112761. using
  112762. acetate
  112763. azides
  112764. organic
  112765. syntheses
  112766. transition
  112767. metal
  112768. complexes
  112769. acylam
  112770. organic
  112771. synthesis
  112772. pressures
  112773. organic
  112774. synthesis
  112775. means
  112776. metal
  112777. carbonyls
  112778. organic
  112779. synthesis
  112780. oxidation
  112781. metal
  112782. compounds
  112783. organic
  112784. synthesis
  112785. concepts
  112786. methods
  112787. starting
  112788. materials
  112789. organic
  112790. synthesis
  112791. roles
  112792. boron
  112793. silicon
  112794. organic
  112795. synthesis
  112796. under
  112797. pressure
  112798. organic
  112799. synthesis
  112800. under
  112801. pressure
  112802. organic
  112803. synthesis
  112804. using
  112805. bridgehead
  112806. carbocations
  112807. bridgehe
  112808. organic
  112809. synthesis
  112810. using
  112811. supported
  112812. reagents
  112813. organic
  112814. synthesis
  112815. utilizing
  112816. cyclobutenyl
  112817. ketones
  112818. organic
  112819. synthesis
  112820. carbonylation
  112821. organometallic
  112822. reagen
  112823. organic
  112824. synthesis
  112825. free-radical
  112826. displacement
  112827. reactions
  112828. organic
  112829. synthesis
  112830. organometallics
  112831. organic
  112832. synthesis
  112833. diazocarbonyl
  112834. compounds
  112835. organic
  112836. synthesis
  112837. a-diazocarbonyl
  112838. compounds
  112839. organic
  112840. synthesis
  112841. oxidative
  112842. enzymes
  112843. organic
  112844. synthesis
  112845. sulfinyl
  112846. oxiranes
  112847. sulfonyl
  112848. oxiran
  112849. organic
  112850. synthesis
  112851. sulfinyloxiranes
  112852. sulfonyloxiranes
  112853. organic-chemistry
  112854. organic-compounds
  112855. organic-reactions
  112856. organic-solvents
  112857. organic-synthesis
  112858. organicphotochemistr
  112859. organics
  112860. organicsynthesis
  112861. organie
  112862. organischen
  112863. organised
  112864. organisms
  112865. organization
  112866. organized
  112867. organizing
  112868. organizing
  112869. principle
  112870. complex
  112871. reactions
  112872. theory
  112873. organlc
  112874. organo
  112875. organo
  112876. organo
  112877. dihalo
  112878. tellurates
  112879. r-tehal2
  112880. organo
  112881. complexes
  112882. aromatic
  112883. compounds
  112884. application
  112885. organo-132-dioxasila
  112886. organo-iron
  112887. organo-iron
  112888. complexes
  112889. aromatic
  112890. compounds
  112891. applications
  112892. organo-lithium
  112893. organo-pi-metal
  112894. organo-silicon
  112895. organo-zirconium
  112896. organoacetylides
  112897. organoactinide
  112898. organoalkali
  112899. organoalkali
  112900. compounds
  112901. radical
  112902. anion
  112903. induced
  112904. reductive
  112905. organoalkali
  112906. reagents
  112907. organoalkaline
  112908. organoaluminium
  112909. organoaluminium
  112910. compounds
  112911. organoaluminium
  112912. reagents
  112913. organoaluminiums
  112914. organoaluminiums
  112915. organic
  112916. synthesis
  112917. organoaluminum
  112918. organoaluminum
  112919. promoted
  112920. direct
  112921. conversion
  112922. aldehydes
  112923. organoaluminum
  112924. promoted
  112925. homologation
  112926. ketones
  112927. diazoal
  112928. organoaluminum
  112929. reagents
  112930. selective
  112931. reactions
  112932. organoaluminums
  112933. organoantimony
  112934. organoarsenic
  112935. organobimetallic
  112936. organobis
  112937. organobismetallic
  112938. organobismetallic
  112939. reagents
  112940. preparation
  112941. synthesis
  112942. organobismetallic
  112943. reagents
  112944. their
  112945. preparation
  112946. organobismuth
  112947. organoborane
  112948. organoborane-mediate
  112949. organoborane-mediate
  112950. synthesis
  112951. functional
  112952. polymers
  112953. organoboranes
  112954. organoborates
  112955. organoborates
  112956. synthetic
  112957. reactions
  112958. organoborates
  112959. organic
  112960. synthesis
  112961. alkenyl
  112962. alkyny
  112963. organoboron
  112964. organoaluminum
  112965. reagents
  112966. selective
  112967. reactions@
  112968. organoboron
  112969. organoboron
  112970. chemistry@
  112971. organochromium
  112972. organocuprates@
  112973. organocuprates
  112974. conjugate
  112975. addition
  112976. reaction@
  112977. organolanthanides
  112978. organomercurials
  112979. organic
  112980. synthesis@
  112981. organometallic
  112982. organometallic
  112983. intermediates
  112984. ultimat
  112985. reagents@
  112986. organometallics-type
  112987. reactions
  112988. aqueous
  112989. media
  112990. challe@
  112991. organophosphorus
  112992. organosilicon
  112993. organostannanes@
  112994. organosulfur
  112995. organotin
  112996. compounds
  112997. organic
  112998. synthesis@
  112999. organotitanium@
  113000. organozirconium
  113001. compounds
  113002. organic
  113003. synthesis@
  113004. orgnnic@
  113005. ortho
  113006. dation
  113007. oxidation
  113008. aldehydes
  113009. carboxylic
  113010. acids
  113011. molecular
  113012. oxidation
  113013. reactions
  113014. using
  113015. magnesium
  113016. monoperphthalate
  113017. oxidative
  113018. cyclizations
  113019. allenic
  113020. sulfonamides
  113021. dimethyl@
  113022. oxides
  113023. oxoalkylation
  113024. carbonyl
  113025. compounds
  113026. conjugated
  113027. nitro
  113028. organoboron
  113029. oboron
  113030. chemistry
  113031. organoboron
  113032. compou
  113033. threefold
  113034. coordinated
  113035. boron
  113036. organoboron
  113037. compounds
  113038. organoboron
  113039. compounds
  113040. introduction
  113041. organoboron
  113042. compounds
  113043. synthetic
  113044. reactions
  113045. organoboron
  113046. compounds
  113047. organic
  113048. synthesis
  113049. introductory
  113050. organoboron
  113051. compounds
  113052. four-to
  113053. sixfold
  113054. coordinated
  113055. boron
  113056. organoboron
  113057. compounds
  113058. fourfold
  113059. coordinated
  113060. boron
  113061. atoms
  113062. organoboron
  113063. compounds
  113064. twofold
  113065. coordinated
  113066. boron
  113067. organoboron
  113068. compounds
  113069. threefold
  113070. coordinated
  113071. boron
  113072. organoboron
  113073. compounds
  113074. threefold
  113075. coordinated
  113076. boron
  113077. atoms
  113078. organoboronic
  113079. organobromine
  113080. organocadmium
  113081. organocerium
  113082. organocerium
  113083. reagents
  113084. organochemical
  113085. organochemistry
  113086. organochlorine
  113087. organochlorosilanes
  113088. organochromium
  113089. organochromium
  113090. organochromium
  113091. compounds
  113092. organochromium
  113093. chemistry
  113094. neglected
  113095. oxidation
  113096. state
  113097. organochromium
  113098. reagents
  113099. organocobalt
  113100. organocobalt
  113101. compounds
  113102. synthesis
  113103. pyridines
  113104. organocobalt-catalyz
  113105. organocobalt-catalyz
  113106. synthesis
  113107. pyridines
  113108. organocopper
  113109. organocopper
  113110. conjugate
  113111. addition
  113112. enolate
  113113. trapping
  113114. reactions
  113115. organocopper
  113116. conjugate
  113117. addition-enolate
  113118. trapping
  113119. reactions
  113120. organocopper
  113121. compounds
  113122. synthesis
  113123. organocopper
  113124. reagents
  113125. organocopper
  113126. reagents
  113127. synthesis
  113128. saturated
  113129. organocopper
  113130. reagents
  113131. substitution
  113132. conjugate
  113133. addition
  113134. carbo
  113135. organocopper
  113136. reagents
  113137. substitution
  113138. conjugate
  113139. addition
  113140. carboc
  113141. organocuprate
  113142. ocuprates
  113143. organocuprates
  113144. ocuprates
  113145. conjugate
  113146. addition
  113147. reaction
  113148. organocyclodisilazan
  113149. organocyclosiloxanes
  113150. organoelement
  113151. organoelement
  113152. derivatives
  113153. 2-pyrone
  113154. their
  113155. applications
  113156. organoelement
  113157. hydroperoxides
  113158. organoelemental
  113159. organofluorine
  113160. organofluorine
  113161. compounds
  113162. medicinal
  113163. chemistry
  113164. biomedic
  113165. organofluorosilanes
  113166. organofluorosilicate
  113167. organohalides
  113168. organohydrosiloxanes
  113169. organohydrotrioxides
  113170. organohydrotrioxides
  113171. diorganotrioxides
  113172. diorganotetroxide
  113173. organoiron
  113174. organoiron
  113175. chemistry
  113176. annual
  113177. survey
  113178. organoiron
  113179. complexes
  113180. potential
  113181. reagen
  113182. organic
  113183. synthe
  113184. organoiron
  113185. compounds
  113186. stoichiometric
  113187. organic
  113188. synthesis
  113189. organolanthanide
  113190. organolanthanides
  113191. organolanthanides
  113192. organolanthanides
  113193. catalysis
  113194. organolanthanoid
  113195. organolanthanoids
  113196. organolead
  113197. organolead
  113198. tricarboxylates
  113199. reagents
  113200. organic
  113201. synth
  113202. organoleptic
  113203. organolithium
  113204. organolithium
  113205. compoundsnindustrial
  113206. applications
  113207. handling
  113208. organolithium
  113209. methods
  113210. organolithium
  113211. methods
  113212. organic
  113213. chemistry
  113214. organolithiums
  113215. organomagnesium
  113216. organomagnesium
  113217. rearrangements
  113218. organomanganese-base
  113219. organomanganous
  113220. organomanganous
  113221. reagents
  113222. their
  113223. organic
  113224. synthesis
  113225. organomercurials
  113226. organomercurials
  113227. organic
  113228. synthesis
  113229. organomercury
  113230. organomercury
  113231. compounds
  113232. organic
  113233. synthesis
  113234. organomet
  113235. organometal
  113236. organometaliic
  113237. organometall
  113238. organometalli
  113239. organometallicT
  113240. organometallic
  113241. organometallic
  113242. organometallic
  113243. carboxamidation
  113244. review
  113245. organometallic
  113246. chemistry
  113247. phase
  113248. organometallic
  113249. chemistry
  113250. arene
  113251. ruthenium
  113252. osmium
  113253. compl
  113254. organometallic
  113255. chemistry
  113256. electrophilic
  113257. transition
  113258. organometallic
  113259. chemistry
  113260. palladium
  113261. platinum
  113262. organometallic
  113263. chemistry
  113264. rhodium
  113265. iridium
  113266. organometallic
  113267. chemistry
  113268. lanthanides
  113269. organometallic
  113270. chemistry
  113271. titanium
  113272. zirconium
  113273. hafnium
  113274. organometallic
  113275. chemistry
  113276. vinyliden
  113277. related
  113278. unsaturate
  113279. organometallic
  113280. compounds
  113281. titanium
  113282. zirconium
  113283. select
  113284. organometallic
  113285. derivatives
  113286. fullerenes
  113287. organometallic
  113288. diazo
  113289. compounds
  113290. organometallic
  113291. intermediates
  113292. ultimat
  113293. reagents
  113294. organometallic
  113295. intermediates
  113296. ultimate
  113297. reagents
  113298. organometallic
  113299. pairs
  113300. organometallic
  113301. lanthanide
  113302. chemistry
  113303. organometallic
  113304. mechanisms
  113305. catalysis
  113306. organometallic
  113307. polysynthons
  113308. novel
  113309. strategy
  113310. selectively
  113311. organometallic
  113312. radical
  113313. processes
  113314. organometallic
  113315. reagents
  113316. synthesis
  113317. organometallic
  113318. sonochemistry
  113319. organometallic
  113320. transformations
  113321. activation
  113322. organometallic
  113323. multiplication
  113324. chirality
  113325. organometallics
  113326. organometallics
  113327. concise
  113328. introduction
  113329. organometallics
  113330. organic
  113331. synthesis
  113332. organometallics
  113333. synthesis
  113334. organometallics-type
  113335. organometallics-type
  113336. reactions
  113337. aqueous
  113338. media
  113339. challe
  113340. organometalloids
  113341. organometauic
  113342. organomethyl
  113343. organomolybdenum
  113344. organonick
  113345. organonickel
  113346. organonickel
  113347. chemistry
  113348. organic
  113349. synthesis
  113350. application
  113351. organonickel
  113352. chemistry
  113353. organic-synthesis
  113354. application
  113355. organonickel
  113356. compounds
  113357. organic
  113358. synthesis
  113359. organonitrogen
  113360. organooxo
  113361. organopalladium
  113362. organopalladium
  113363. complexes
  113364. palladium
  113365. oxidation
  113366. organopalladium
  113367. compounds
  113368. organic
  113369. synthesis
  113370. cataly
  113371. organopalladium
  113372. intermediates
  113373. organic
  113374. synthesis
  113375. organoperoxides
  113376. organoperoxysulfonic
  113377. organoperoxysulfonic
  113378. acids
  113379. their
  113380. derivatives
  113381. organophospho
  113382. organophosphorus
  113383. organophosphorus
  113384. organophosphorus
  113385. thiocyanidates
  113386. their
  113387. structural
  113388. organoplatinium
  113389. organopolysilanes
  113390. organopotassium
  113391. organopseudohalosila
  113392. organopseudohalosila
  113393. azidosilanes
  113394. organorhenium
  113395. organorhenium
  113396. chemistry
  113397. organorhodium
  113398. organoruthenium
  113399. organosamarium
  113400. organoselenium
  113401. organoselenium
  113402. chemistry
  113403. organoselenium
  113404. chemistry
  113405. functional
  113406. group
  113407. transformations
  113408. organoselenium
  113409. reagents
  113410. tandem
  113411. fragmentation
  113412. cycliz
  113413. organosilanes
  113414. organosilanes
  113415. radical
  113416. based
  113417. reducing
  113418. agents
  113419. synthesis
  113420. organosilanes
  113421. radical-based
  113422. reducing
  113423. agents
  113424. synthesis
  113425. organosilic
  113426. organosilicon
  113427. organosilicon
  113428. organosilicon
  113429. bioorganosilicon
  113430. chemistry
  113431. structure
  113432. bondi
  113433. organosilicon
  113434. organotin
  113435. compounds
  113436. synthesis
  113437. organosilicon
  113438. compounds
  113439. nucleophiles
  113440. synthesis
  113441. organosilicon
  113442. compounds
  113443. reagents
  113444. organic
  113445. chemistry
  113446. organosilicon
  113447. compounds
  113448. organic
  113449. synthesis
  113450. organosilicon
  113451. compounds
  113452. introduction
  113453. organosilicon
  113454. synthesis
  113455. isocyanates
  113456. organosilicon
  113457. transition
  113458. metal
  113459. ractions
  113460. organosilicone
  113461. organosilicone
  113462. compounds
  113463. organic
  113464. synthesis
  113465. organosilicons
  113466. organosiloxanes
  113467. organosiloxanes
  113468. functional
  113469. groups
  113470. short
  113471. review
  113472. organosiloxazanes
  113473. organosodium
  113474. organosodium
  113475. organopotassium
  113476. compounds
  113477. organosulfonyloxy
  113478. organosulfur
  113479. organosulfur
  113480. organosulphur
  113481. organotellurium
  113482. organotellurium
  113483. compounds
  113484. introduction
  113485. organotellurium
  113486. cyanides
  113487. tellurium
  113488. dicyanides
  113489. r-te-cn
  113490. organotetrahalotellu
  113491. organotetrahalotellu
  113492. r-te-hal4
  113493. organotetrazenes
  113494. organotetrazenes
  113495. higher
  113496. homologues
  113497. organothallium
  113498. organothallium
  113499. chemistry
  113500. organothio
  113501. organothio
  113502. chloroacetylenes
  113503. polyfunctional
  113504. reagents
  113505. organothiophosphorus
  113506. organotin
  113507. organotin
  113508. alkoxide
  113509. review
  113510. increased
  113511. nucleophilicity
  113512. without
  113513. organotin
  113514. chemistry
  113515. organotin
  113516. cluster
  113517. chemistry
  113518. organotin
  113519. compounds
  113520. organic
  113521. synthesis
  113522. organotin
  113523. enolates
  113524. organic
  113525. synthesis
  113526. organotin
  113527. enolates
  113528. organic
  113529. synthesis
  113530. review
  113531. organotin
  113532. heterocycles
  113533. organotin
  113534. hydride
  113535. catalyzed
  113536. carbon-carbon
  113537. formation
  113538. eagents
  113539. organotitanium
  113540. reagents
  113541. organic
  113542. synthesis
  113543. organotr
  113544. organotr
  113545. azenes
  113546. organotransition
  113547. organotransition
  113548. metal
  113549. chemistry
  113550. organotransition
  113551. metallic
  113552. chemistry
  113553. sulfur
  113554. dioxide
  113555. analog
  113556. organotransition-met
  113557. organozinc
  113558. organozinc
  113559. diimine
  113560. radicals
  113561. synthesis
  113562. reactivity
  113563. towar
  113564. organozinc
  113565. organocadmium
  113566. organomercury
  113567. reagents
  113568. organozincs
  113569. organozirconium
  113570. organozirconium
  113571. chemistry
  113572. revisited
  113573. surface
  113574. things
  113575. organozirconium
  113576. compounds
  113577. organic
  113578. synthesis
  113579. organylmetal
  113580. orgin
  113581. oriando
  113582. orientation
  113583. orientational
  113584. orientations
  113585. oriented
  113586. origin
  113587. original
  113588. original
  113589. syntheses
  113590. epoxides
  113591. involving
  113592. noselenium
  113593. origins
  113594. origins
  113595. stereoselectivity
  113596. addition
  113597. allyl
  113598. oriquat
  113599. orlandi
  113600. orlandi
  113601. giorgio
  113602. zerbetto
  113603. francesco
  113604. zgierski
  113605. marek
  113606. theoreti
  113607. orlando
  113608. orlinkov
  113609. orlinkov
  113610. akhrem
  113611. vol'pin
  113612. structure
  113613. equimol
  113614. orlov
  113615. orlov
  113616. polarography
  113617. coumarins
  113618. chromen
  113619. orlova
  113620. ormiston
  113621. oroheterocyclic
  113622. orqanomet
  113623. ortho
  113624. ortho
  113625. ortho
  113626. esters
  113627. dialkoxycarbenium
  113628. reactivity
  113629. stability
  113630. ortho
  113631. metalation
  113632. directed
  113633. amino
  113634. alkoxides
  113635. article
  113636. ortho-aminoaldehydes
  113637. ortho-bromoacetanili
  113638. ortho-functionallity
  113639. ortho-manganated
  113640. ortho-manganated
  113641. ketones
  113642. related
  113643. compounds
  113644. organ
  113645. ortho-quinodimethane
  113646. orthocarbonates
  113647. orthocarbonic
  113648. orthocarbonic
  113649. derivatives
  113650. orthocarboxylic
  113651. orthocarboxylic
  113652. derivatives
  113653. orthocyclophanesy
  113654. orthoester
  113655. orthoesters
  113656. orthogonal
  113657. ogonal
  113658. molecular
  113659. descriptors
  113660. orthoman
  113661. orthomanganated
  113662. orthomanganated
  113663. ketones
  113664. related
  113665. compo
  113666. organi
  113667. orthoquinodimethanes
  113668. orthosomycins
  113669. ortiz
  113670. osaka
  113671. osamu
  113672. osawa
  113673. osawa
  113674. osawa
  113675. yonemitsu
  113676. osamu
  113677. carbocyclic
  113678. compounds
  113679. osborn
  113680. osborne
  113681. oscar
  113682. oshea
  113683. oshima
  113684. oshry
  113685. osipov
  113686. osipov
  113687. kolomiets
  113688. fokin
  113689. fluorine
  113690. containing
  113691. ketim
  113692. osladin
  113693. osmaoxetane
  113694. osmium
  113695. osmium
  113696. tetroxide
  113697. hydroxylation
  113698. unsaturated
  113699. substrates
  113700. osmium-catalyzed
  113701. proof
  113702. characterization
  113703. soccer-ba
  113704. osokin
  113705. osterberg
  113706. ostercamp
  113707. osterhout
  113708. osterhout
  113709. martin
  113710. nadler
  113711. william
  113712. padwa
  113713. albert
  113714. recent
  113715. ostovic
  113716. ostovic
  113717. drazen
  113718. bruice
  113719. thomas
  113720. mechanism
  113721. alkene
  113722. epoxidati
  113723. ostrovskii
  113724. oswald
  113725. otake
  113726. otera
  113727. otera
  113728. junzo
  113729. template
  113730. effects
  113731. distannoxanes
  113732. advances
  113733. otera
  113734. junzo
  113735. transesterification
  113736. chemical
  113737. reviews
  113738. other
  113739. other
  113740. diazinodiazines
  113741. other
  113742. fused-ring
  113743. azetidines
  113744. azetines
  113745. azetes
  113746. other
  113747. imidazoles
  113748. fused
  113749. six-membered
  113750. rings
  113751. othiocarbonyl
  113752. otohiko
  113753. otsuji
  113754. otsuka
  113755. otsuka
  113756. kazuhide
  113757. catalytic
  113758. asymmetric
  113759. hydrogen
  113760. migra
  113761. synthesis
  113762. stable
  113763. isotopes
  113764. carbon
  113765. nitrogen
  113766. martin
  113767. noordik
  113768. computer
  113769. tools
  113770. reaction
  113771. retri
  113772. ottenbrite
  113773. ottenheijm
  113774. ottens
  113775. ottolenghi
  113776. ottolenghi
  113777. photochemistry
  113778. rhodopsins
  113779. ottorino
  113780. ottosson
  113781. ouarcarmycins
  113782. oudemansin
  113783. oudemansins
  113784. ourisson
  113785. ourisson
  113786. albrecht
  113787. pierre
  113788. hopanoids
  113789. geohopanoids
  113790. ourisson
  113791. rohmer
  113792. michel
  113793. hopanoids
  113794. geohopanoids
  113795. novel
  113796. outcome
  113797. outer
  113798. outline
  113799. ovalent
  113800. ovaska
  113801. ovcharenkoJ
  113802. ovchinnikov
  113803. overall
  113804. overberger
  113805. overcome
  113806. overcoming
  113807. overcrowded
  113808. overlap
  113809. overlook
  113810. overman
  113811. overman
  113812. allylic
  113813. propargylic
  113814. imidic
  113815. esters
  113816. organic
  113817. overman
  113818. application
  113819. intramolecular
  113820. reactions
  113821. overman
  113822. larry
  113823. abelman
  113824. matthew
  113825. kucera
  113826. david
  113827. overman
  113828. larry
  113829. charge
  113830. component
  113831. reaction
  113832. design
  113833. overproduction
  113834. overton
  113835. overton
  113836. picken
  113837. secondary
  113838. metabolism
  113839. plant
  113840. tissu
  113841. overton
  113842. stereochemical
  113843. choice
  113844. enzymic
  113845. reactions
  113846. overview
  113847. overwhelmed
  113848. ovrutskii
  113849. owsley
  113850. ox/n-acetals
  113851. ox/n-acetals
  113852. linear
  113853. o-c-n
  113854. structure
  113855. oxa-di
  113856. oxa-di
  113857. methane
  113858. photoisomerizations
  113859. oxabicyclic
  113860. cyclo
  113861. oxabutadienes
  113862. oxacephems
  113863. oxacycle
  113864. oxacyclic
  113865. oxadi
  113866. oxadiazino
  113867. oxadiazoles
  113868. oxadiazoline
  113869. oxadiazolines
  113870. oxadienes
  113871. oxahept
  113872. oxallyl
  113873. oxalyl
  113874. oxamides
  113875. oxanes
  113876. oxanorbornyl
  113877. oxaspiro
  113878. oxathiane
  113879. oxathiazoles
  113880. oxathiazolium
  113881. oxathiazolium
  113882. compounds
  113883. oxathioacetal
  113884. oxathiole
  113885. oxatriazetidines
  113886. oxatriazoles
  113887. oxatriazoles
  113888. thiatriazoles
  113889. oxatricyclo
  113890. oxaza
  113891. oxazaborolidine
  113892. oxazaborolidine
  113893. catalyzed
  113894. enantioselective
  113895. reductions
  113896. oxazaborolidines
  113897. oxazaborolidines
  113898. dioxaborolidines
  113899. enantioselective
  113900. oxazaphosphole
  113901. oxazaspiro
  113902. oxazepin
  113903. oxazetidines
  113904. oxazin
  113905. oxazine
  113906. oxazines
  113907. oxazines
  113908. thiazines
  113909. their
  113910. benzo
  113911. derivatives
  113912. oxaziridine
  113913. oxaziridines
  113914. oxazole
  113915. oxazole
  113916. alkaloids
  113917. oxazole
  113918. chemistry
  113919. review
  113920. recent
  113921. advances
  113922. oxazoles
  113923. oxazoles
  113924. their
  113925. benzo
  113926. derivatives
  113927. oxazolidines
  113928. oxazolidinone
  113929. oxazolidinones
  113930. oxazoline
  113931. oxazolines
  113932. oxazolone
  113933. oxazolones
  113934. oxazolopiperidines
  113935. oxazolopiperidones
  113936. oxenoid
  113937. oxepane
  113938. oxepanes
  113939. oxepins
  113940. thiepanes
  113941. thiepins
  113942. oxepin
  113943. oxepines
  113944. oxepinones
  113945. oxepins
  113946. oxetane
  113947. oxetanes
  113948. oxetanes
  113949. oxetenes
  113950. oxetenes
  113951. oxford
  113952. oxidantv
  113953. oxidants
  113954. oxidase
  113955. oxidatiions
  113956. oxidation
  113957. oxidation
  113958. oxidation
  113959. adjacent
  113960. bonds
  113961. oxidation
  113962. adjacent
  113963. bonds
  113964. dehydrogenation
  113965. oxidation
  113966. adjacent
  113967. bonds
  113968. hydroxylation
  113969. methods
  113970. oxidation
  113971. adjacent
  113972. nitrogen
  113973. oxidation
  113974. adjacent
  113975. oxygen
  113976. alcohols
  113977. other
  113978. methods
  113979. oxidation
  113980. adjacent
  113981. oxygen
  113982. alcohols
  113983. activated
  113984. oxidation
  113985. adjacent
  113986. oxygen
  113987. alcohols
  113988. chromium
  113989. reagent
  113990. oxidation
  113991. adjacent
  113992. oxygen
  113993. ethers
  113994. oxidation
  113995. adjacent
  113996. sulfur
  113997. oxidation
  113998. chemical
  113999. methods
  114000. oxidation
  114001. electrochemical
  114002. methods
  114003. oxidation
  114004. microbial
  114005. methods
  114006. oxidation
  114007. nitrene
  114008. insertion
  114009. oxidation
  114010. remote
  114011. functionalization
  114012. methods
  114013. oxidation
  114014. inhibition
  114015. organic
  114016. materials
  114017. oxidation
  114018. introduction
  114019. oxidation
  114020. alcohols
  114021. activated
  114022. dimethyl
  114023. sulfoxide
  114024. oxidation
  114025. alcohols
  114026. carbonyl
  114027. compounds
  114028. alkoxysulfon
  114029. oxidation
  114030. aldehydes
  114031. carboxylic
  114032. acids
  114033. molecular
  114034. oxidation
  114035. allylic
  114036. methylene
  114037. groups
  114038. under
  114039. oxidation
  114040. amines
  114041. dichlorodicyanoquino
  114042. trappin
  114043. oxidation
  114044. epoxyalkyl
  114045. trimethylsilane
  114046. pyridine
  114047. oxidation
  114048. biologically
  114049. interesting
  114050. amines
  114051. hydroxylamin
  114052. oxidation
  114053. carbon-boron
  114054. bonds
  114055. oxidation
  114056. carbon-halogen
  114057. bonds
  114058. oxidation
  114059. carbon-metal
  114060. bonds
  114061. oxidation
  114062. carbon-silicon
  114063. bonds
  114064. oxidation
  114065. five-membered
  114066. heterocycles
  114067. containing
  114068. oxidation
  114069. hydrazones
  114070. aminoaryl
  114071. ketones
  114072. synthe
  114073. oxidation
  114074. acylindoles
  114075. dimethyldioxirane
  114076. singlet
  114077. oxidation
  114078. olefins
  114079. mercuric
  114080. salts
  114081. oxidation
  114082. organometallic
  114083. compounds
  114084. oxidation
  114085. organic-compounds
  114086. aqueous
  114087. bromine
  114088. solut
  114089. oxidation
  114090. sulfur
  114091. selenium
  114092. tellurium
  114093. oxidation
  114094. weakly
  114095. activated
  114096. bonds
  114097. oxidation
  114098. weakly
  114099. activated
  114100. bonds
  114101. oxidation
  114102. reactions
  114103. using
  114104. magnesium
  114105. monoperphthalate
  114106. oxidation
  114107. using
  114108. manganese
  114109. dioxide
  114110. oxidations
  114111. oxidations
  114112. organic
  114113. chemistry
  114114. oxidations
  114115. potassium
  114116. nitrosodisulfonate
  114117. fremy's
  114118. radical
  114119. oxidative
  114120. oxidative
  114121. attachment
  114122. arenesulfonyloxy
  114123. groups
  114124. arenesu
  114125. oxidative
  114126. cleavage
  114127. substituted
  114128. cycloalkane
  114129. diones
  114130. oxidative
  114131. coupling
  114132. oxidative
  114133. coupling
  114134. organocopper
  114135. reagents
  114136. oxidative
  114137. cyclizations
  114138. allenic
  114139. sulfonamides
  114140. dimethyl
  114141. oxidative
  114142. decarboxylation
  114143. carboxylic
  114144. acids
  114145. tetraa
  114146. oxidative
  114147. decarboxylution
  114148. acids
  114149. tetraacetate
  114150. oxidative
  114151. degradation
  114152. nucleic
  114153. acids
  114154. oxidative
  114155. radical
  114156. additions
  114157. a-nitro
  114158. ketones
  114159. oxidative
  114160. decarboxylation
  114161. unsaturated
  114162. carboxylic
  114163. oxidative
  114164. intramolecular
  114165. cycloaddition
  114166. silylene
  114167. prote
  114168. oxidative
  114169. radical
  114170. cyclization
  114171. iodoalkyl
  114172. indoles
  114173. oxidative
  114174. rearrangement
  114175. reactions
  114176. oxidatively
  114177. oxide
  114178. oxides
  114179. oxides
  114180. oxidized
  114181. oxidizing
  114182. oxido
  114183. oxidosqualene
  114184. oxime
  114185. oximes
  114186. oxindolacetic
  114187. oxindole
  114188. oxindoles
  114189. oxirane
  114190. oxiranes
  114191. oxiranes
  114192. oxirenes
  114193. oxiranyl
  114194. oxiranylallylsilanes
  114195. oxiranylcarbinyl/all
  114196. oxirene
  114197. oxirenes
  114198. oxirenes
  114199. preparation
  114200. chemistry
  114201. imino
  114202. functionalized
  114203. oxazetidines
  114204. overview
  114205. imino-functionalized
  114206. 12-oxazetidines
  114207. overview
  114208. polyene
  114209. macrolide
  114210. antibiotics
  114211. oxo-metalloporphyrin
  114212. oxoalkanoates
  114213. oxoalkylation
  114214. oxoalkylation
  114215. carbonyl
  114216. compounds
  114217. conjugated
  114218. nitro
  114219. oxobut
  114220. oxocanes
  114221. oxocarbenium
  114222. oxocarbon
  114223. oxocarbons
  114224. oxocarbons
  114225. pseudooxocarbons
  114226. oxochromiumamine
  114227. oxochromiumporphyrin
  114228. oxodecahydroisoquino
  114229. oxodihydroisoxazoles
  114230. oxogelsemine
  114231. oxohex
  114232. oxoindolin
  114233. oxoketene
  114234. oxoketene
  114235. acetals
  114236. versatile
  114237. intermediates
  114238. organic
  114239. synthes
  114240. oxoketenes
  114241. oxolysine
  114242. oxomanganese
  114243. oxone
  114244. oxonia
  114245. oxoniobates
  114246. oxoniobates
  114247. containing
  114248. metal
  114249. clusters
  114250. oxonium
  114251. oxonium
  114252. organic
  114253. synthesis
  114254. oxopipecolic
  114255. oxopyrimidines
  114256. oxoquinoline
  114257. oxotitanium
  114258. oxovincadifformine
  114259. diazo
  114260. carbonyl
  114261. compounds
  114262. rhodium
  114263. mediated
  114264. decompositi
  114265. oxy-cope
  114266. oxy-palladation
  114267. oxyacids
  114268. oxyalkylation
  114269. oxyalkylation
  114270. carbonyl
  114271. compounds
  114272. conjugated
  114273. nitro
  114274. oxyallyl
  114275. oxyallyls
  114276. oxyanionic
  114277. oxycarbamate
  114278. oxycarbenes
  114279. oxycarbenium
  114280. oxycarbonyl
  114281. oxycarbonylnitrenes
  114282. oxycyclopropanes
  114283. oxycyclopropanes
  114284. organochemical
  114285. synthesis
  114286. oxyfunctionalization
  114287. oxyfunctionalization
  114288. reactions
  114289. perfluoro
  114290. dialkylox
  114291. oxygen
  114292. oxy-palladation@
  114293. oxygen
  114294. ozonides
  114295. aldehyde
  114296. protecting
  114297. groups
  114298. protecting
  114299. courtot
  114300. rumin
  114301. salaun
  114302. photochemistry
  114303. polyenes
  114304. hemmerich
  114305. flavin
  114306. flavocoenzyme
  114307. chemistry
  114308. braca
  114309. carbon
  114310. monoxide
  114311. addition
  114312. acetylenic
  114313. p-benzyne@
  114314. padwa
  114315. albert
  114316. krumpe
  114317. keith
  114318. application
  114319. intramolecular
  114320. paladacycles
  114321. structurally
  114322. defined
  114323. catalysts
  114324. palladium
  114325. palladium
  114326. catalysed
  114327. asymmetric
  114328. allylic
  114329. substitution
  114330. ligand@
  114331. palladium
  114332. catalyzed
  114333. carbonylative
  114334. cross
  114335. coupling
  114336. reactions
  114337. palladium
  114338. catalyzed
  114339. hydrogenation
  114340. unsaturated
  114341. sulfone@
  114342. palladium
  114343. catalyzed
  114344. synthesis
  114345. optically
  114346. active
  114347. tetrahy@
  114348. palladium-catalyzed@
  114349. panayotov@
  114350. papers
  114351. paramagnetic@
  114352. parrott@
  114353. parts
  114354. patai
  114355. chemistry
  114356. ketenes
  114357. allenes
  114358. related
  114359. comp@
  114360. pathways
  114361. oxygen
  114362. oxygen
  114363. nitrogen-assisted
  114364. lithiation
  114365. carbolithiation
  114366. oxygen
  114367. oxidation
  114368. reagent
  114369. oxygen
  114370. carbon
  114371. effects
  114372. radical
  114373. reactions
  114374. oxygen
  114375. insertion
  114376. reactions
  114377. bridged
  114378. bicyclic
  114379. ketones
  114380. oxygen-containing
  114381. oxygen-nitrogen-oxyg
  114382. oxygen-transfer
  114383. oxygenated
  114384. oxygenationD
  114385. oxygenation
  114386. silyl
  114387. ethers
  114388. silyl
  114389. ketene
  114390. acetals
  114391. oxygenations
  114392. oxygenolysis
  114393. oxylipins
  114394. oxylylene
  114395. oxynitrenes
  114396. oxypalladation
  114397. oxyphosphonium
  114398. oxyphosphoranes
  114399. oxyxen
  114400. ozawa
  114401. ozbalik
  114402. ozonation
  114403. ozone
  114404. ozone
  114405. oxidation
  114406. reagent
  114407. ozonides
  114408. ozonides
  114409. aldehyde
  114410. protecting
  114411. groups
  114412. protecting
  114413. ozonization
  114414. ozonolysis
  114415. ozonolysis
  114416. fullerene
  114417. ozonolysis
  114418. vinyl
  114419. ethers
  114420. ozonolytic
  114421. grieco
  114422. synthesis
  114423. methods
  114424. synthesis
  114425. b-containing
  114426. heterocycles
  114427. p-c-o-b
  114428. c-o-b
  114429. accounts
  114430. silver
  114431. assisted
  114432. reactions
  114433. meyers
  114434. stereo
  114435. energies
  114436. alkylations
  114437. tautomeric
  114438. heterocyclic
  114439. courtot
  114440. rumin
  114441. salaun
  114442. photochemistry
  114443. polyenes
  114444. cyclizations
  114445. methoxycarbonyl
  114446. oxycarbenium
  114447. synthe
  114448. ellis
  114449. ditchfield
  114450. theory
  114451. indirect
  114452. nuclear
  114453. kennewell
  114454. taylor
  114455. magnus
  114456. recent
  114457. developments
  114458. sulfone
  114459. chemistry
  114460. eaton
  114461. tetrahedron
  114462. symposium
  114463. print
  114464. eaton
  114465. branca
  114466. shankar
  114467. tetrahedron
  114468. georghiou
  114469. chemistry
  114470. vitamin
  114471. hormone
  114472. calciferols
  114473. eparation
  114474. organoaluminium
  114475. compounds
  114476. organic
  114477. eparation
  114478. labelled
  114479. arenes
  114480. facial
  114481. diastereoselection
  114482. cycloadditions
  114483. facial
  114484. stereoselectivities
  114485. diels
  114486. alder
  114487. cycloadditions
  114488. sammes
  114489. recent
  114490. chemistry
  114491. sammes
  114492. recent
  114493. studies
  114494. gilgen
  114495. heimgartner
  114496. schmid
  114497. hansen
  114498. review
  114499. hemmerich
  114500. flavin
  114501. flavocoenzyme
  114502. chemistry
  114503. hodge
  114504. sherrington
  114505. polymer
  114506. second
  114507. garratt
  114508. symposium
  114509. novel
  114510. aromati
  114511. scheuer
  114512. marine
  114513. toxins
  114514. accounts
  114515. chemical
  114516. scheuer
  114517. tetrahedron
  114518. organic
  114519. chemistry
  114520. smith
  114521. organic
  114522. synthesis
  114523. organ
  114524. smith
  114525. london
  114526. organic
  114527. synthesis
  114528. wagner
  114529. effects
  114530. methyl
  114531. substitution
  114532. rates
  114533. triple
  114534. fuchs
  114535. braish
  114536. multiply
  114537. conve
  114538. watson
  114539. parshall
  114540. organola
  114541. laszlo
  114542. catalysis
  114543. organic
  114544. react
  114545. lavalle
  114546. phase
  114547. transfer
  114548. catalysis
  114549. henry
  114550. lange
  114551. oxidation
  114552. groups
  114553. nanjappan
  114554. czarnik
  114555. metal
  114556. braca
  114557. carbon
  114558. monoxide
  114559. addition
  114560. acetylenic
  114561. braca
  114562. carbon
  114563. monoxide
  114564. addition
  114565. acetylenic
  114566. piacenti
  114567. bianchi
  114568. hydrocarboxylation
  114569. olefin
  114570. piacenti
  114571. bianchi
  114572. reactions
  114573. carbon
  114574. monoxide
  114575. stacking
  114576. effects
  114577. asymmetric
  114578. synthesis
  114579. vollhardt
  114580. fortschritte
  114581. forschung
  114582. jolly
  114583. angew
  114584. allylpall
  114585. p-450
  114586. p-allyl
  114587. p-allylnickel
  114588. p-arene
  114589. p-benzoquinone
  114590. p-bond
  114591. p-bromocarbocations
  114592. p-c-n-b
  114593. p-c-o-b
  114594. p-chiral
  114595. p-complexes
  114596. p-halogen-substitute
  114597. p-halogen-substitute
  114598. phosphorus
  114599. ylids
  114600. p-ligand
  114601. p-peptide
  114602. p-toluenesulfinyl
  114603. p-toluenesulphonates
  114604. metal
  114605. catalyzed
  114606. cyclization
  114607. reactions
  114608. hydrocarbons
  114609. paaren
  114610. pabilities
  114611. pacheco
  114612. paciorek
  114613. paciorek
  114614. kratzer
  114615. stability
  114616. perfluoroalkylethers
  114617. paddon
  114618. paddon
  114619. michael
  114620. investigating
  114621. range
  114622. electron
  114623. trans
  114624. paderes
  114625. padwa
  114626. padwa
  114627. austin
  114628. ligand
  114629. effects
  114630. chemoselectivity
  114631. padwa
  114632. blacklock
  114633. rieker
  114634. synthesis
  114635. polycyclic
  114636. padwa
  114637. carlsen
  114638. kamigata
  114639. photochemical
  114640. constructio
  114641. padwa
  114642. excited
  114643. state
  114644. chemistry
  114645. cyclopropene
  114646. derivatives
  114647. padwa
  114648. photochemical
  114649. rearrangements
  114650. membered
  114651. padwa
  114652. photochemical
  114653. transformations
  114654. cyclopropene
  114655. deriva
  114656. padwa
  114657. albert
  114658. fryxell
  114659. cyclization
  114660. cycloaddition
  114661. padwa
  114662. albert
  114663. hornbuckle
  114664. susan
  114665. ylide
  114666. formation
  114667. padwa
  114668. albert
  114669. krumpe
  114670. keith
  114671. application
  114672. intramolecular
  114673. padwa
  114674. albert
  114675. murphree
  114676. shaum
  114677. recent
  114678. developments
  114679. padwa
  114680. albert
  114681. murphree
  114682. shaun
  114683. cycloaddition
  114684. cyclization
  114685. padwa
  114686. albert
  114687. murphree
  114688. shaun
  114689. recent
  114690. developments
  114691. paeoniflorigenin
  114692. paeoniflorin
  114693. paeoniforin
  114694. paetow
  114695. paetzold
  114696. paganelli
  114697. michael
  114698. chemistry
  114699. lactams
  114700. blackie
  114701. academi
  114702. pagni
  114703. pagodane
  114704. polycyclic
  114705. aromatic
  114706. hydrocarbons
  114707. fullerene
  114708. pahor
  114709. paine
  114710. painter
  114711. pairing
  114712. pairs
  114713. pairwise
  114714. paknikar
  114715. pakusch
  114716. palacios
  114717. paladacycles
  114718. paladacycles
  114719. structurally
  114720. defined
  114721. catalysts
  114722. palasinski
  114723. palazon
  114724. palazzo
  114725. paleta
  114726. palladiumC
  114727. palladium
  114728. lkoxyal
  114729. palladium
  114730. catalyzed
  114731. coupling
  114732. reactions
  114733. alkoxy
  114734. ethyn
  114735. palladium
  114736. catalyzed
  114737. thioboration
  114738. terminal
  114739. alkynes
  114740. palladium
  114741. platinum-catalyzed
  114742. addition
  114743. aldehydes
  114744. palladium
  114745. and/or
  114746. copper
  114747. mediated
  114748. cross
  114749. coupling
  114750. reactions
  114751. palladium
  114752. assisted
  114753. reactions
  114754. olefins
  114755. cyclize
  114756. palladium
  114757. carbenoids
  114758. enolates
  114759. sulfonyl
  114760. acetyleni
  114761. palladium
  114762. catalysed
  114763. addition
  114764. masked
  114765. formyl
  114766. cyanides
  114767. palladium
  114768. catalysed
  114769. alkylative
  114770. cyclisation
  114771. butadianylm
  114772. palladium
  114773. catalysed
  114774. asymmetric
  114775. allylic
  114776. substitution
  114777. ligand
  114778. palladium
  114779. catalysed
  114780. asymmetric
  114781. hydroalkenylation
  114782. norborne
  114783. palladium
  114784. catalysed
  114785. carbonyl
  114786. allylation
  114787. isoprene
  114788. palladium
  114789. catalysed
  114790. cross
  114791. coupling
  114792. vinyl
  114793. triflates
  114794. palladium
  114795. catalysed
  114796. cyclisation
  114797. cyclopropanation
  114798. cycliza
  114799. palladium
  114800. catalyzed
  114801. addition
  114802. activated
  114803. methylene
  114804. palladium
  114805. catalyzed
  114806. addition
  114807. alkyne
  114808. norbornene
  114809. derivat
  114810. palladium
  114811. catalyzed
  114812. amination
  114813. iodides
  114814. catalyzed
  114815. annulation
  114816. 14-dienes
  114817. using
  114818. ortho-func
  114819. palladium
  114820. catalyzed
  114821. aromatic
  114822. amination
  114823. generate
  114824. palladium
  114825. catalyzed
  114826. aromatic
  114827. aminations
  114828. generat
  114829. palladium
  114830. catalyzed
  114831. arylation
  114832. alkyl
  114833. allyl
  114834. carbamates
  114835. palladium
  114836. catalyzed
  114837. carbonyl
  114838. allylation
  114839. allylpalladium
  114840. palladium
  114841. catalyzed
  114842. carbonylative
  114843. cycloaddition
  114844. palladium
  114845. catalyzed
  114846. carbonylative
  114847. cross
  114848. coupling
  114849. reaction
  114850. palladium
  114851. catalyzed
  114852. carbonylative
  114853. cross
  114854. coupling
  114855. reactions
  114856. palladium
  114857. catalyzed
  114858. chemoselective
  114859. reaction
  114860. allylic
  114861. carbo
  114862. palladium
  114863. catalyzed
  114864. cocyclization
  114865. allenes
  114866. electron
  114867. palladium
  114868. catalyzed
  114869. cross
  114870. coupling
  114871. arene
  114872. chromium
  114873. tricarb
  114874. palladium
  114875. catalyzed
  114876. cross
  114877. coupling
  114878. arene-chromium
  114879. tricarb
  114880. palladium
  114881. catalyzed
  114882. cross
  114883. coupling
  114884. halides
  114885. olefi
  114886. palladium
  114887. catalyzed
  114888. cross
  114889. coupling
  114890. reaction
  114891. alkoxydiboron
  114892. palladium
  114893. catalyzed
  114894. cross
  114895. coupling
  114896. reactions
  114897. organoboroni
  114898. palladium
  114899. catalyzed
  114900. cyclization
  114901. carbonylation
  114902. allylic
  114903. palladium
  114904. catalyzed
  114905. cycloisomerization
  114906. 12-dialkylidenecyc
  114907. palladium
  114908. catalyzed
  114909. cycloisomerizations
  114910. enynes
  114911. relate
  114912. palladium
  114913. catalyzed
  114914. dehydrative
  114915. aromatization
  114916. cyclohexeno
  114917. palladium
  114918. catalyzed
  114919. enantioselective
  114920. allylic
  114921. substitution
  114922. palladium
  114923. catalyzed
  114924. formation
  114925. carbon-nitrogen
  114926. bonds
  114927. react
  114928. palladium
  114929. catalyzed
  114930. hydrogenation
  114931. unsaturated
  114932. sulfone
  114933. palladium
  114934. catalyzed
  114935. hydrogenolysis
  114936. alkynyl
  114937. formates
  114938. palladium
  114939. catalyzed
  114940. iodine
  114941. exchange
  114942. reactions
  114943. palladium
  114944. catalyzed
  114945. polyene
  114946. cyclizations
  114947. approach
  114948. palladium
  114949. catalyzed
  114950. reaction
  114951. dichloroethenes
  114952. palladium
  114953. catalyzed
  114954. reactions
  114955. organic
  114956. halides
  114957. olefin
  114958. palladium
  114959. catalyzed
  114960. reactions
  114961. organotin
  114962. compounds
  114963. palladium
  114964. catalyzed
  114965. reduction
  114966. sulfonates
  114967. selectivity
  114968. palladium
  114969. catalyzed
  114970. reductive
  114971. coupling
  114972. chlorides
  114973. palladium
  114974. catalyzed
  114975. substitution
  114976. unsaturated
  114977. lactones
  114978. oxidation
  114979. terminal
  114980. alkenes
  114981. methyl
  114982. palladium
  114983. complex
  114984. catalyzed
  114985. reductive
  114986. heterocyclization
  114987. palladium
  114988. complex
  114989. potassium
  114990. carbonate
  114991. catalysed
  114992. reductive
  114993. palladium
  114994. copper
  114995. cocatalyzed
  114996. coupling
  114997. stereodefine
  114998. palladium
  114999. assisted
  115000. reactions
  115001. monoolefins
  115002. palladium
  115003. catalyzed
  115004. synthesis
  115005. optically
  115006. active
  115007. tetrahy
  115008. palladium
  115009. organic
  115010. synthesis
  115011. palladium
  115012. organic
  115013. synthesis
  115014. tetrahedron
  115015. symposium
  115016. palladium
  115017. selective
  115018. oxidation
  115019. reactions
  115020. palladium
  115021. mediated
  115022. intramolecular
  115023. formation
  115024. between
  115025. palladium
  115026. mediated
  115027. methylenecyclopropan
  115028. opening
  115029. applica
  115030. palladium
  115031. mediated
  115032. stereo
  115033. regioselective
  115034. tandem
  115035. cyclizat
  115036. palladium
  115037. nickel-catalysed
  115038. cross
  115039. coupling
  115040. selective
  115041. palladium
  115042. promoted
  115043. synthesis
  115044. 7-deoxyprekinamycin
  115045. palladium
  115046. promoted
  115047. synthesis
  115048. ionophore
  115049. antibiotics
  115050. strate
  115051. palladium
  115052. reagents
  115053. organic
  115054. synthesis
  115055. palladium-c
  115056. palladium-ca
  115057. palladium-ca
  115058. alyzed
  115059. polyene
  115060. cyclizations
  115061. palladium-cat
  115062. palladium-catalysed
  115063. palladium-catalysed
  115064. oxidation
  115065. hydrocarbons
  115066. palladium-catalysed
  115067. synthesis
  115068. heterocycles
  115069. palladium-catalysed
  115070. vinylation
  115071. organic
  115072. halides
  115073. palladium-catalyzed
  115074. arylation
  115075. vinylation
  115076. 4-alkyl
  115077. palladium-catalyzed
  115078. arylation
  115079. allylic
  115080. diols
  115081. highly
  115082. select
  115083. palladium-catalyzed
  115084. carbonyl
  115085. allylation
  115086. allylpalladium
  115087. palladium-catalyzed
  115088. cross-coupling
  115089. reactions
  115090. organoboroni
  115091. palladium-catalyzed
  115092. cyclization
  115093. halloallenes
  115094. palladium-catalyzed
  115095. cycloisomerization
  115096. enynes
  115097. related
  115098. palladium-catalyzed
  115099. enantioselective
  115100. allylic
  115101. substitution
  115102. palladium-catalyzed
  115103. intramolecular
  115104. 14-additions
  115105. conjugate
  115106. palladium-catalyzed
  115107. reactions
  115108. organotin
  115109. compounds
  115110. palladium-catalyzed
  115111. vinylic
  115112. substitution
  115113. palladium-mediated
  115114. palladium-mediated
  115115. arylation
  115116. ethers
  115117. palladium/copper
  115118. palmer
  115119. palou
  115120. palou
  115121. oxidation
  115122. organic
  115123. compounds
  115124. aqueous
  115125. bromi
  115126. palytoxin
  115127. palyulin
  115128. pamela
  115129. panayotov
  115130. pancracine
  115131. pancratistatin
  115132. pandey
  115133. tiwari
  115134. lactones
  115135. building
  115136. pandey
  115137. tiwari
  115138. recent
  115139. advances
  115140. chemistry
  115141. pandey
  115142. ganesh
  115143. photoinduced
  115144. electron
  115145. transfer
  115146. organic
  115147. pandey
  115148. ganesh
  115149. synthetic
  115150. perspectives
  115151. photoinduced
  115152. electro
  115153. pandiewicz
  115154. pandiewicz
  115155. krzysztof
  115156. watanabe
  115157. kyoichi
  115158. synthesis
  115159. pandit
  115160. pandit
  115161. upendra
  115162. programmed
  115163. antibodies
  115164. tailor
  115165. cataly
  115166. paneque
  115167. panetta
  115168. panetta
  115169. charles
  115170. heimer
  115171. norman
  115172. hussey
  115173. charles
  115174. metzger
  115175. panico
  115176. panico
  115177. robert
  115178. powell
  115179. warren
  115180. richer
  115181. claude
  115182. guide
  115183. pankaj
  115184. pankaja
  115185. pankratov
  115186. pannell
  115187. panov
  115188. panunzio
  115189. panza
  115190. paola
  115191. paolini
  115192. paolo
  115193. papageorgiou
  115194. papagni
  115195. papaveraceae
  115196. papers
  115197. papers
  115198. papina
  115199. pappalardo
  115200. papuamine
  115201. paquette
  115202. paquette
  115203. investigations
  115204. furanocembranolide
  115205. diterpen
  115206. paquette
  115207. chemistry
  115208. silylcyclopropanes
  115209. paquette
  115210. development
  115211. polyquinane
  115212. chemistry
  115213. paquette
  115214. evolution
  115215. heptalene
  115216. chemistry
  115217. paquette
  115218. ramberg
  115219. backlund
  115220. rearrangement
  115221. paquette
  115222. realities
  115223. extended
  115224. homoaromaticity
  115225. paquette
  115226. carbonyl
  115227. group
  115228. regeneration
  115229. substantive
  115230. paquette
  115231. current
  115232. dynamic
  115233. change
  115234. within
  115235. para-substituted
  115236. paracyclophane
  115237. paracyclophanes
  115238. paradigm
  115239. paradigms
  115240. paradoxes
  115241. paraffinic
  115242. paraffins
  115243. paraherquamide
  115244. parallel
  115245. paralytic
  115246. paramagnetic
  115247. parameter
  115248. parameters
  115249. paraperiodate
  115250. parasorbic
  115251. paration
  115252. pardo
  115253. pardo
  115254. santelli
  115255. synthesis
  115256. parekh
  115257. parent
  115258. parham
  115259. paride
  115260. parish
  115261. parish
  115262. mossbauer
  115263. spectroscopy
  115264. organic
  115265. chemistry
  115266. pariza
  115267. pariza
  115268. freiberg
  115269. erythromycin
  115270. chemistry
  115271. excited
  115272. state
  115273. intermediates
  115274. probed
  115275. parker
  115276. parker
  115277. david
  115278. determination
  115279. enantiomeric
  115280. purity
  115281. chemic
  115282. parker
  115283. novel
  115284. methods
  115285. synthesis
  115286. glycosi
  115287. parkin
  115288. parkin
  115289. gerard
  115290. stretch
  115291. isomerism
  115292. transition
  115293. metal
  115294. parmar
  115295. parmar
  115296. prasad
  115297. sinha
  115298. taneja
  115299. poonam
  115300. parmerter
  115301. parmon
  115302. parnes
  115303. parrott
  115304. parry
  115305. parshall
  115306. parshall
  115307. homogeneous
  115308. catalysis
  115309. applications
  115310. parsons
  115311. parsons
  115312. simon
  115313. passmore
  115314. rings
  115315. radicals
  115316. synthetic
  115317. partV
  115318. asarathy
  115319. parthasarathy
  115320. determination
  115321. relative
  115322. absolute
  115323. confi
  115324. partial
  115325. partial
  115326. complete
  115327. reduction
  115328. pyridines
  115329. their
  115330. benzo
  115331. partial
  115332. complete
  115333. reductions
  115334. pyrroles
  115335. furans
  115336. thiophene
  115337. partial
  115338. complete
  115339. reduction
  115340. heterocycles
  115341. containing
  115342. partial
  115343. reduction
  115344. aromatic
  115345. rings
  115346. dissolving
  115347. metals
  115348. partial
  115349. reduction
  115350. enones
  115351. styrenes
  115352. related
  115353. systems
  115354. partially
  115355. participants
  115356. participation
  115357. particles
  115358. particular
  115359. partition
  115360. partitioning
  115361. partitioning
  115362. carbanion
  115363. intermediates
  115364. generated
  115365. alcohol
  115366. partner
  115367. partners
  115368. parts
  115369. parts
  115370. parvez
  115371. parviflorin
  115372. pascal
  115373. pascal
  115374. robert
  115375. tormented
  115376. aromatic
  115377. compounds
  115378. pashinnik
  115379. pashkevich
  115380. pashkevich
  115381. saloutin
  115382. postavskii
  115383. fluorine
  115384. contain
  115385. pashkovskii
  115386. pasquato
  115387. pasqui
  115388. passerini
  115389. passive
  115390. passmore
  115391. pasto
  115392. pasto
  115393. daniel
  115394. johnson
  115395. miller
  115396. marvin
  115397. experiments
  115398. pasto
  115399. daniel
  115400. taylor
  115401. richard
  115402. reduction
  115403. diimide
  115404. pastor
  115405. pastushenko
  115406. pasynskii
  115407. pataiN
  115408. patai
  115409. chemistry
  115410. cyanates
  115411. their
  115412. derivatives
  115413. patai
  115414. chemistry
  115415. diazonium
  115416. diazo
  115417. groups
  115418. wiley
  115419. patai
  115420. chemistry
  115421. carbon
  115422. carbon
  115423. triple
  115424. parts
  115425. patai
  115426. chemistry
  115427. ketenes
  115428. allenes
  115429. related
  115430. patai
  115431. chemistry
  115432. organic
  115433. arsenic
  115434. antimony
  115435. patai
  115436. supplement
  115437. chemistry
  115438. derivatives
  115439. patai
  115440. patai's
  115441. guide
  115442. chemistry
  115443. functional
  115444. patai
  115445. rappoport
  115446. supplement
  115447. chemistry
  115448. patai
  115449. rappoport
  115450. chemistry
  115451. alkanes
  115452. patai
  115453. rappoport
  115454. chemistry
  115455. amidines
  115456. patai
  115457. rappoport
  115458. chemistry
  115459. sulfonic
  115460. acids
  115461. patai's
  115462. patane
  115463. patchornik
  115464. patelj
  115465. paterno
  115466. paterno-buchi
  115467. paterson
  115468. paterson
  115469. berrisford
  115470. david
  115471. epoxides
  115472. asymmetric
  115473. paterson
  115474. methods
  115475. strategies
  115476. stereocontro
  115477. paths
  115478. pathwaym
  115479. pathways
  115480. pathways
  115481. electrophilic
  115482. aromatic
  115483. substitution
  115484. cyclohexadie
  115485. paton
  115486. patonay
  115487. patonay
  115488. gabor
  115489. detection
  115490. newer
  115491. methods
  115492. patricia
  115493. patrick
  115494. patrizia
  115495. pattenden
  115496. pattenden
  115497. natural
  115498. ylidenebutenolides
  115499. ylidenetetron
  115500. pattenden
  115501. photon
  115502. synthesis
  115503. chemistry
  115504. pattenden
  115505. gerald
  115506. synthetic
  115507. studies
  115508. natural
  115509. oxazoles
  115510. pattern
  115511. patterns
  115512. patterns
  115513. stoichiometric
  115514. catalytic
  115515. reactions
  115516. organo
  115517. patterson
  115518. patwardhan
  115519. patwardhan
  115520. synthesis
  115521. alkanediols
  115522. review
  115523. paudler
  115524. paula
  115525. pauling's
  115526. paulsen
  115527. paulson
  115528. pauson
  115529. pauson-khand
  115530. paust
  115531. recent
  115532. progress
  115533. commercial
  115534. retinoids
  115535. caroteno
  115536. pavel
  115537. pavlenko
  115538. pavlova
  115539. pavlova
  115540. komarova
  115541. davidovish
  115542. rogozhin
  115543. aspart
  115544. pawan
  115545. pawlak
  115546. payneE
  115547. payne
  115548. rearrangement
  115549. tosyl
  115550. epoxides
  115551. functionalized
  115552. paust@
  115553. pederin
  115554. pelter
  115555. andrew
  115556. robert
  115557. reactions
  115558. 26-diaryl
  115559. dioxab@
  115560. pentacooridinated@
  115561. pentafulvalenes@
  115562. peptide
  115563. peptido-mimetics
  115564. receptor
  115565. ligands-discovery
  115566. development
  115567. perchlorate/oxygen@
  115568. perchlorotriphenylen@
  115569. perfluoroalkylation
  115570. initiated
  115571. sodium
  115572. dithionite
  115573. perfluoroisobutene@
  115574. pericyclic
  115575. reactions
  115576. biological-systems
  115577. biomimeti
  115578. pericyclic
  115579. reactions
  115580. organic
  115581. synthesis
  115582. biosynthesis
  115583. permeability
  115584. peroxy
  115585. perspectives
  115586. peters
  115587. ravindranathan
  115588. brown
  115589. mechanistic
  115590. probe
  115591. petrov
  115592. rudnev
  115593. sorokin
  115594. sulfenamides
  115595. their
  115596. pharmacology
  115597. phase-transfer
  115598. phenomenon
  115599. radical
  115600. anion
  115601. fragmentation
  115602. course
  115603. phenylethylamines@
  115604. philadelphia
  115605. phorbol@
  115606. phosphate
  115607. phosphodiesters@
  115608. otochemical
  115609. catalysed
  115610. coupling
  115611. cyclopropenylzinc
  115612. chlorides
  115613. catalysed
  115614. intramolecular
  115615. coupling
  115616. between
  115617. tertiary
  115618. amines
  115619. catalyzed
  115620. cycloisomerization
  115621. dialkylidenecycloalk
  115622. catalyzed
  115623. cycloisomerization
  115624. dialkylidenecycloalk
  115625. pd-catalyzed
  115626. pd/tppts
  115627. peach
  115628. peach
  115629. bailery
  115630. reactions
  115631. azides
  115632. indoles
  115633. pearce
  115634. pearsonb
  115635. pearson
  115636. cyclohexadienes
  115637. second
  115638. supplements
  115639. pearson
  115640. compounds
  115641. organic
  115642. synthesis
  115643. academic
  115644. pearson
  115645. tricarbonyl
  115646. diene
  115647. complexes
  115648. synthetically
  115649. pearson
  115650. anthony
  115651. multiple
  115652. stereocontrol
  115653. using
  115654. organometalli
  115655. pebrenko
  115656. pechmann
  115657. pecific
  115658. peculiar
  115659. peculiarities
  115660. peculiarities
  115661. reactivity
  115662. telluriumorganic
  115663. compound
  115664. peddinti
  115665. pederin
  115666. pederin
  115667. pedersen
  115668. pedersen
  115669. synthetic
  115670. multidentate
  115671. macrocyclic
  115672. compounds
  115673. pederson
  115674. pedro
  115675. pedrocchi
  115676. norton
  115677. letourneau
  115678. michael
  115679. synthesis
  115680. angular
  115681. pegas
  115682. peifer
  115683. peijnenburg
  115684. peijnenburg
  115685. structure
  115686. activity
  115687. relationships
  115688. peishoff
  115689. pelcman
  115690. pelikan
  115691. pelizzetti
  115692. pelizzi
  115693. pellerite
  115694. pellerite
  115695. brauman
  115696. phase
  115697. acidities
  115698. carbon
  115699. pelletier
  115700. pelletier
  115701. chemistry
  115702. diterpenoid
  115703. pelletier
  115704. structure
  115705. synthesis
  115706. pelletier
  115707. william
  115708. alkaloids
  115709. chemical
  115710. biological
  115711. pelter
  115712. pelter
  115713. rearrangements
  115714. involving
  115715. boron
  115716. rearrangements
  115717. pelter
  115718. andrew
  115719. chemistry
  115720. hindered
  115721. organoboranes
  115722. pelter
  115723. andrew
  115724. robert
  115725. reactions
  115726. 26-diaryl
  115727. dioxab
  115728. pelyvas
  115729. pendant
  115730. penem
  115731. penems
  115732. penetrated
  115733. penglis
  115734. penglis
  115735. fluorinated
  115736. carbohydrates
  115737. advances
  115738. peniciilins
  115739. penicillin
  115740. penicillins
  115741. penkovsky
  115742. penne
  115743. penning
  115744. penny
  115745. penta
  115746. pentaaryl
  115747. pentacarbonyl
  115748. pentacarbonyl-cataly
  115749. pentachloride
  115750. pentachlorides
  115751. pentacoordinate
  115752. pentacoordinate
  115753. fluorosilicate
  115754. anion
  115755. pentacoordinated
  115756. pentacyclic
  115757. pentacyclo
  115758. pentadeoxy
  115759. pentadienals
  115760. pentadienoate
  115761. pentadienyl
  115762. pentadienyl-metal
  115763. pentadienylsilane
  115764. pentaenoic
  115765. pentafluoride
  115766. pentafluorophenol
  115767. pentafluorophenyl
  115768. pentafulvalenes
  115769. pentafulvenes
  115770. pentahalides
  115771. pentahalophenyl
  115772. pentahapto-dienyl
  115773. pentakis
  115774. pentalene
  115775. pentalene
  115776. dihydropentalenes
  115777. pentalenolactones
  115778. pentamethylcyclopent
  115779. pentane
  115780. pentanes
  115781. pentapeptide
  115782. pentaphenylbismuth
  115783. pentaprismane
  115784. pentaranes
  115785. pentasaccharide
  115786. pentasil
  115787. pentasubstituted
  115788. pentatetraenes
  115789. pentatrienes
  115790. pentazines
  115791. pentazoles
  115792. pentenyl
  115793. penzlin
  115794. pepleomycin
  115795. pepper
  115796. peptide
  115797. peptide
  115798. peptide
  115799. protein
  115800. synthesis
  115801. segment
  115802. synthesi
  115803. condensati
  115804. peptide
  115805. chemistry
  115806. practical
  115807. textbook
  115808. peptide
  115809. cyclizations
  115810. solid
  115811. support
  115812. efficient
  115813. peptide
  115814. pharmaceuticals
  115815. approaches
  115816. design
  115817. novel
  115818. peptide
  115819. secondary
  115820. structure
  115821. mimetics
  115822. recent
  115823. advances
  115824. peptidesU
  115825. peptido
  115826. peptido-mimetics
  115827. peptido-mimetics
  115828. receptor
  115829. ligands-discovery
  115830. development
  115831. peptidoglycan
  115832. peptidomimetic
  115833. peptidomimetic
  115834. fused
  115835. bicyclic
  115836. lactams
  115837. acylim
  115838. peptidomimetic
  115839. synthesis
  115840. freidinger
  115841. lactams
  115842. peptidomimetics
  115843. peptidomimetics
  115844. tailored
  115845. enzyme-inhibitors
  115846. peptidyl
  115847. peptite
  115848. peptoid
  115849. peptoids
  115850. peptoids
  115851. approach
  115852. development
  115853. pharmaceut
  115854. peracetic
  115855. peracid
  115856. peracids
  115857. peracids
  115858. radicals
  115859. theoretical
  115860. experimental
  115861. percarboxylic
  115862. percarboxylic
  115863. acids
  115864. including
  115865. metal
  115866. salts
  115867. perchec
  115868. percheron
  115869. percheron
  115870. francois
  115871. courtois
  115872. emile
  115873. perchlorate
  115874. /oxygen
  115875. perchlorates
  115876. perchloro
  115877. perchloro-organic
  115878. perchloro-organic
  115879. chemistry
  115880. structures
  115881. spectroscopy
  115882. perchlorotriphenylen
  115883. peregudov
  115884. pereira
  115885. pereira
  115886. schubert
  115887. srebnik
  115888. morris
  115889. ireland
  115890. claisen
  115891. rearrang
  115892. perekalinM
  115893. perekalin
  115894. lipina
  115895. berestovitskaya
  115896. efremov
  115897. peres
  115898. peresypkina
  115899. perez
  115900. perfect
  115901. perfluoralkane
  115902. perfluorinated
  115903. perfluorinated
  115904. carbon
  115905. chain
  115906. copolymers
  115907. functional
  115908. group
  115909. perfluorinated
  115910. resinsulphonic
  115911. nafion-h
  115912. catalysis
  115913. perfluoro
  115914. perfluoro-oxa-alkano
  115915. perfluoro-oxa-alkyla
  115916. perfluoroalkane
  115917. perfluoroalkanesulfo
  115918. perfluoroalkanesulhp
  115919. perfluoroalkanesulhp
  115920. esters
  115921. methods
  115922. preparation
  115923. appli
  115924. perfluoroalkanoates
  115925. perfluoroalkanoyl
  115926. perfluoroalkyl
  115927. perfluoroalkyl
  115928. acetylenes
  115929. perfluoroalkyl-subst
  115930. perfluoroalkylation
  115931. perfluoroalkylation
  115932. initiated
  115933. sodium
  115934. dithionite
  115935. perfluoroalkylethers
  115936. perfluoroalkyllithiu
  115937. perfluoroarenes
  115938. perfluoroarenes
  115939. novel
  115940. selective
  115941. protecting
  115942. reagents
  115943. perfluorobutyrate
  115944. perfluorocarboxamide
  115945. perfluorohexanes
  115946. performance
  115947. perfumes
  115948. pergamon
  115949. perhalomethanesulphe
  115950. perhydro
  115951. perhydro
  115952. histrionicotoxin
  115953. perhydrofuro
  115954. perhydrohistrionicot
  115955. perhydrophenanthrene
  115956. peri-annelated
  115957. peri-condensed
  115958. periasamy
  115959. peric
  115960. perichon
  115961. pericyclic
  115962. pericyclic
  115963. reactions
  115964. biological-systems
  115965. biomimeti
  115966. pericyclic
  115967. reactions
  115968. biological-systems
  115969. biomimeti
  115970. pericyclic
  115971. reaction
  115972. transition
  115973. states
  115974. pericyclic
  115975. reactions
  115976. biological
  115977. systems-does
  115978. nature
  115979. pericyclic
  115980. reactions
  115981. vinylallenes
  115982. calciferols
  115983. pericyclization
  115984. pericyclization
  115985. vinylallenes
  115986. organic
  115987. synthesis
  115988. perie
  115989. perimeter
  115990. perimidines
  115991. periodates
  115992. periodic
  115993. periodic
  115994. oxidation
  115995. periodic
  115996. oxidation
  115997. ernest
  115998. jackson
  115999. organic
  116000. reactions
  116001. periplanone
  116002. periplanone
  116003. total
  116004. synthesis
  116005. intramolecular
  116006. pinacol
  116007. coupl
  116008. periselectivity
  116009. perkin
  116010. perkins
  116011. perkins
  116012. trapping
  116013. 1981171
  116014. advances
  116015. physical
  116016. organ
  116017. perkyns
  116018. perlin
  116019. perlmutter
  116020. perlmutter
  116021. conjugate
  116022. addition
  116023. reactions
  116024. organic
  116025. synthes
  116026. perlstein
  116027. permangana
  116028. permanganate
  116029. permeability
  116030. permeability
  116031. permethylated
  116032. permethyltellimagran
  116033. permitivity
  116034. permittivity
  116035. pernitriles
  116036. perovskone
  116037. peroxid
  116038. peroxide
  116039. peroxides
  116040. peroxides
  116041. ozonization
  116042. peroxides
  116043. photosensitized
  116044. oxidation
  116045. heteroatom
  116046. compo
  116047. peroxidic
  116048. peroxo
  116049. peroxo
  116050. compounds
  116051. oxidation
  116052. reagents
  116053. peroxo
  116054. compounds
  116055. reagents
  116056. organic
  116057. chemistry
  116058. reactions
  116059. peroxometal
  116060. peroxometal
  116061. complexes
  116062. derived
  116063. hydrogen
  116064. peroxide
  116065. peroxonium
  116066. peroxy
  116067. peroxy
  116068. peroxy
  116069. acids
  116070. peroxy
  116071. esters
  116072. peroxy
  116073. iminocarboxylic
  116074. acids
  116075. peroxy
  116076. natural
  116077. products
  116078. peroxydisulfate
  116079. peroxydisulphuryl
  116080. peroxygen
  116081. peroxyl
  116082. peroxysulfur
  116083. perphosphinic
  116084. perphosphinic
  116085. acids
  116086. perphosphonic
  116087. acids
  116088. their
  116089. derivative
  116090. perphosphonic
  116091. perplexed
  116092. perrin
  116093. perrin
  116094. armarego
  116095. perrin
  116096. purification
  116097. laborator
  116098. perrio
  116099. perron
  116100. perrone
  116101. perruthenatev
  116102. persistent
  116103. personal
  116104. persoons
  116105. perspective
  116106. perspectives
  116107. perspectives
  116108. perspectives
  116109. supramolecular
  116110. chemistry
  116111. molecular
  116112. perspecuity
  116113. persulfate
  116114. perturbation
  116115. perturbed
  116116. pertussis
  116117. perutz
  116118. perutz
  116119. robin
  116120. organometallic
  116121. intermediates
  116122. ultimatereagents
  116123. pervalent
  116124. perylenequinones
  116125. peshawarine
  116126. pestellini
  116127. pesticides
  116128. reactions
  116129. aromatic
  116130. compounds
  116131. pet-reactions
  116132. pet-reactions
  116133. aromatic
  116134. mpounds
  116135. petaisis
  116136. petasis
  116137. petasis
  116138. nicos
  116139. patane
  116140. michael
  116141. synthesis
  116142. carbocycli
  116143. peter
  116144. peters
  116145. peters
  116146. ravindranathan
  116147. brown
  116148. mechanistic
  116149. probe
  116150. peters
  116151. synthesis
  116152. bicyclo
  116153. 3.3.1
  116154. nonanes
  116155. synth
  116156. peters
  116157. moldowan
  116158. biomarker
  116159. guide
  116160. interpreting
  116161. petersen
  116162. peterson
  116163. peterson
  116164. olefination
  116165. reaction
  116166. using
  116167. trimethylgermyl
  116168. acetate
  116169. petit
  116170. petitou
  116171. petitou
  116172. boeckel
  116173. chemical
  116174. synthesis
  116175. heparin
  116176. petra
  116177. petragnani
  116178. petragnani
  116179. comasseto
  116180. tellurium
  116181. reagents
  116182. organic
  116183. petragnani
  116184. nicola
  116185. tellurium
  116186. organic
  116187. synthesis
  116188. academic
  116189. petrarch
  116190. petrini
  116191. petroleum
  116192. petros
  116193. petrosyan
  116194. petrov
  116195. petrov
  116196. rudnev
  116197. sorokin
  116198. sulfenamides
  116199. their
  116200. petrova
  116201. petrovskii
  116202. petrzilka
  116203. petrzilka
  116204. grayson
  116205. preparation
  116206. diels
  116207. alder
  116208. reaction
  116209. pettit
  116210. pettit
  116211. bryostatins
  116212. pettitt
  116213. petty
  116214. peyman
  116215. armor
  116216. chemistry
  116217. titanocene
  116218. zirconocene
  116219. pezzuto
  116220. pfaff
  116221. pfaltz
  116222. pfaltz
  116223. andreas
  116224. chiral
  116225. semicorrins
  116226. related
  116227. nitrogen
  116228. heter
  116229. pfander
  116230. pfander
  116231. carotenoids
  116232. carotenoids
  116233. pfander
  116234. stoll
  116235. terpenoid
  116236. glycosides
  116237. natura
  116238. pfander
  116239. stoll
  116240. terpenoid
  116241. glycosides
  116242. natural
  116243. pfeffer
  116244. pfeffer
  116245. michel
  116246. selected
  116247. applications
  116248. organic
  116249. synthesis
  116250. pfenninger
  116251. pfleiderer
  116252. pfleiderer
  116253. wolfgang
  116254. pteridines
  116255. properties
  116256. reactivities
  116257. ph2po
  116258. ph3snh
  116259. phakmazie
  116260. phakmazie
  116261. chemical
  116262. enzymatic
  116263. methods
  116264. phamacology
  116265. phanes
  116266. pharm
  116267. pharmaceutical
  116268. pharmaceuticals
  116269. pharmacokinetic
  116270. pharmacological
  116271. pharmacology
  116272. pharmacology
  116273. pharmacophore
  116274. pharmazie
  116275. phaset
  116276. phase
  116277. transfer
  116278. assisted
  116279. permanganate
  116280. oxidatiions
  116281. phase
  116282. transfer
  116283. catalysis
  116284. phase
  116285. transfer
  116286. catalysis
  116287. organometallic
  116288. chemistry
  116289. phase
  116290. transfer
  116291. catalysis
  116292. chemistry
  116293. catalysts
  116294. applica
  116295. phase
  116296. transfer
  116297. catalysis
  116298. selected
  116299. problems
  116300. applications
  116301. phase
  116302. transfer
  116303. catalysts
  116304. phase-transfer
  116305. phase-transfer
  116306. phase-transfer
  116307. catalysed
  116308. two-phase
  116309. reactions
  116310. preparative
  116311. phase-transfer
  116312. catalysis
  116313. fundamentals
  116314. applications
  116315. indus
  116316. phase-transfer
  116317. reactions
  116318. phases
  116319. phenacyl
  116320. phenacylides
  116321. phenalenone
  116322. phenalenones
  116323. phenantbroline
  116324. phenanthraquinone
  116325. phenanthrene
  116326. phenanthrenecarboxyl
  116327. phenanthrenes
  116328. phenanthridines
  116329. phenanthroindolizidi
  116330. phenanthroline
  116331. phenanthrolines
  116332. phenanthroquinolizid
  116333. phenazine
  116334. phene
  116335. phenethylamines
  116336. phenethylisoquinolin
  116337. phenol
  116338. phenolates
  116339. phenolic
  116340. phenolic
  116341. compounds
  116342. mulberry
  116343. related
  116344. plants
  116345. phenols
  116346. phenomena
  116347. phenomenon
  116348. phenomenon
  116349. radical
  116350. anion
  116351. fragmentation
  116352. course
  116353. phenothiazine
  116354. phenothiazines
  116355. phenothiazines
  116356. 14-benzothiazines
  116357. chemical
  116358. biomedical
  116359. phenoxazine
  116360. phenoxide
  116361. phenoxy
  116362. phenoxyquinolines
  116363. phenyl
  116364. phenyl
  116365. trihalomethyl
  116366. mercury
  116367. compounds
  116368. exceptionally
  116369. versati
  116370. phenyl-substituted
  116371. phenylacetylene
  116372. phenylalaninate
  116373. phenylalkanesulfamoy
  116374. phenylalkanoic
  116375. phenylalkynes
  116376. phenylcopper
  116377. phenylcopper
  116378. diphenylcuprate
  116379. characterization
  116380. phenyldiazoacetates
  116381. phenyldimethylsilyl
  116382. phenyldimethylsilyl
  116383. alcohol
  116384. surrogate
  116385. intramolecula
  116386. phenyldisilanes
  116387. phenylene
  116388. phenylenes
  116389. phenylethylamines
  116390. phenylethylamines
  116391. isoquinoline
  116392. alkaloids
  116393. phenylimidates
  116394. phenylisoquinoline
  116395. phenylisoserine
  116396. phenylisothiazoles
  116397. phenylmethoxy
  116398. phenylmethyl
  116399. phenyloxazol
  116400. phenylpyrrole
  116401. phenylquinolines
  116402. phenylselenide
  116403. phenylseleno
  116404. phenylselenophthalim
  116405. phenylsufonylhydrazo
  116406. phenylsulfanyl
  116407. phenylsulfinyl
  116408. phenylsulfinylethyl
  116409. phenylsulfones
  116410. phenylsulfonyl
  116411. phenylsulfonyloxazir
  116412. phenylsulfoxonium
  116413. phenyltelluro
  116414. phenylthiazoles
  116415. phenylthio
  116416. phenylthioazetidinon
  116417. phenylthiocyclopropy
  116418. phenylthioethynyl
  116419. phenylthiopentenynes
  116420. pheromone
  116421. pheromones
  116422. pheromones
  116423. organoboranes
  116424. short
  116425. convenient
  116426. synthe
  116427. philadelphia
  116428. philadelphia
  116429. philic
  116430. philip
  116431. philippe
  116432. phillip
  116433. phillipe
  116434. phillips
  116435. philosophy
  116436. philp
  116437. philp
  116438. douglas
  116439. stoddart
  116440. fraser
  116441. assembly
  116442. organic
  116443. phleichrome
  116444. phosgenammonium
  116445. phosgene
  116446. phosph
  116447. phospha
  116448. phospha-alkene
  116449. phospha-wittig
  116450. phosphaalkene
  116451. phosphaalkenes
  116452. phosphaalkynes
  116453. phosphaalkynes
  116454. phosphaalkenes
  116455. phosphaalkynes
  116456. building
  116457. blocks
  116458. synthetic
  116459. chemistry
  116460. phosphaallene
  116461. phosphaallenes
  116462. phosphabenzenes
  116463. phosphacumulene
  116464. phosphacumulene
  116465. ylides
  116466. phospha-alkene
  116467. ylides
  116468. phosphaethylenes
  116469. phosphane
  116470. phosphanes
  116471. phosphanorbornene
  116472. phosphatase
  116473. phosphate
  116474. phosphate
  116475. phosphates
  116476. phosphatides
  116477. phosphazanes
  116478. phosphazenes
  116479. phosphene
  116480. phosphenylidene
  116481. phosphides
  116482. phosphin
  116483. phosphin-imine
  116484. phosphinates
  116485. phosphindole
  116486. phosphine
  116487. phosphine-boranes
  116488. phosphine/tetrachlor
  116489. phosphinephosphite
  116490. phosphines
  116491. phosphinic
  116492. phosphinidene
  116493. phosphinidenes
  116494. phosphinidenylidene
  116495. phosphinimides
  116496. phosphinimines
  116497. phosphinous
  116498. phosphinyl
  116499. phosphinyldiazometha
  116500. phosphinylidene
  116501. phosphirenes
  116502. phosphite
  116503. phosphite
  116504. synthesis
  116505. oligodeoxyribonucleo
  116506. phospho
  116507. phospho
  116508. alkynes
  116509. phospho
  116510. alkenes
  116511. phosphodiester
  116512. phosphodiesters
  116513. phospholanes
  116514. phosphole
  116515. phospholipids
  116516. phospholipids
  116517. handbook
  116518. phosphonate
  116519. phosphonate-containi
  116520. phosphonates
  116521. phosphonium
  116522. phosphonobutanoic
  116523. phosphonous
  116524. phosphoramidite
  116525. phosphorane
  116526. phosphoranes
  116527. phosphoranides
  116528. phosphoranyl
  116529. phosphoranylidene
  116530. phosphoranylideneket
  116531. phosphoranylideneket
  116532. thioketene
  116533. ketenimines
  116534. phosphoric
  116535. phosphorines
  116536. phosphorins
  116537. phosphorodithioate
  116538. phosphorodithioates
  116539. phosphorothioate
  116540. phosphorothioates
  116541. phosphorous
  116542. phosphoru
  116543. phosphoru
  116544. compounds
  116545. coordination
  116546. number
  116547. phosphorus
  116548. phosphorus
  116549. phosphorus
  116550. addition
  116551. carbon
  116552. phosphorus
  116553. derivatives
  116554. salicylic
  116555. phosphorus
  116556. compounds
  116557. coordination
  116558. number
  116559. phosphinid
  116560. phosphorus
  116561. compounds
  116562. ordination
  116563. number
  116564. phosphin
  116565. phosphorus
  116566. compounds
  116567. coordination
  116568. number
  116569. iminopho
  116570. phosphorus
  116571. compounds
  116572. coordination
  116573. number
  116574. l3-phosp
  116575. phosphorus
  116576. compounds
  116577. coordination
  116578. number
  116579. methylen
  116580. phosphorus
  116581. compounds
  116582. coordination
  116583. number
  116584. organoox
  116585. phosphorus
  116586. compounds
  116587. coordination
  116588. number
  116589. phosphan
  116590. phosphorus
  116591. compounds
  116592. coordination
  116593. number
  116594. phosphin
  116595. phosphorus
  116596. compounds
  116597. coordination
  116598. number
  116599. phosphon
  116600. phosphorus
  116601. compounds
  116602. coordination
  116603. number
  116604. phosphor
  116605. phosphorus
  116606. compounds
  116607. coordination
  116608. number
  116609. alkylidene
  116610. phosphorus
  116611. compounds
  116612. phosphonium
  116613. phosphorus
  116614. compounds
  116615. coordination
  116616. number
  116617. phosphorus
  116618. compounds
  116619. coordination
  116620. number
  116621. l5-phospho
  116622. phosphorus
  116623. compounds
  116624. coordination
  116625. number
  116626. phosphane
  116627. phosphorus
  116628. compounds
  116629. coordination
  116630. number
  116631. phosphinic
  116632. phosphorus
  116633. compounds
  116634. coordination
  116635. number
  116636. phosphonic
  116637. phosphorus
  116638. compounds
  116639. coordination
  116640. number
  116641. phosphoric
  116642. phosphorus
  116643. compounds
  116644. coordination
  116645. number
  116646. phosphorus
  116647. phosphorus
  116648. compounds
  116649. coordination
  116650. number
  116651. phosphorus
  116652. compounds
  116653. phosphorus-carbon
  116654. phosphorus-containin
  116655. phosphorus-containin
  116656. alkyl
  116657. alkenyl
  116658. sulphonyl
  116659. phosphorus-containin
  116660. nucleophiles
  116661. reactions
  116662. polyfluo
  116663. phosphorus-stabilise
  116664. phosphorus-strong
  116665. phosphoryl
  116666. horyl-stabilise
  116667. phosphorylated
  116668. phosphorylating
  116669. phosphorylation
  116670. phosphorylative
  116671. phosphorylcarbenes
  116672. phosphorylstabilized
  116673. phosphosulfates
  116674. phosphotriester
  116675. photo
  116676. photo-fries
  116677. photo-fries
  116678. rearrangement
  116679. photo-induced
  116680. photo-oxidation
  116681. photo-oxygenation
  116682. photo-reduction
  116683. photo-reduction
  116684. photo-oxidation
  116685. photoaddition
  116686. photoadditions
  116687. photoadditions
  116688. dialkylcuprate
  116689. additions
  116690. butyl
  116691. photoadduct
  116692. photoannulation
  116693. photoassociation
  116694. photobehavior
  116695. photocatalysis
  116696. photocatalysis
  116697. transition
  116698. metal
  116699. complexes
  116700. photocatalytic
  116701. photocatalyzed
  116702. photocatalyzed
  116703. multiple
  116704. additions
  116705. amines
  116706. b-unsaturat
  116707. photochem
  116708. photochem
  116709. deuterium
  116710. isotope
  116711. effect
  116712. photorearrangement
  116713. photochemical
  116714. photochemical
  116715. photochemical
  116716. cyanoethylation
  116717. indoles
  116718. photochemical
  116719. cleavage
  116720. alkylphosphonic
  116721. photochemical
  116722. cyclisations
  116723. intramolecular
  116724. cycloadditions
  116725. photochemical
  116726. cycloaddition
  116727. reactions
  116728. enones
  116729. alkenes
  116730. photochemical
  116731. cycloadditions
  116732. photochemical
  116733. decomposition
  116734. benzocyclobutenone
  116735. toluenes
  116736. photochemical
  116737. deprotection
  116738. 5'-dimethoxybenzoin
  116739. photochemical
  116740. electron
  116741. transfer
  116742. reactions
  116743. applications
  116744. photochemical
  116745. hydroxylation
  116746. aromatic
  116747. compounds
  116748. photochemical
  116749. one-way
  116750. adiabatic
  116751. isomerization
  116752. aromatic
  116753. photochemical
  116754. reactions
  116755. organised
  116756. assemblies
  116757. environmenta
  116758. photochemical
  116759. reactions
  116760. methoxy
  116761. enones
  116762. isolation
  116763. photochemical
  116764. rearrangements
  116765. fragmentation
  116766. benzene
  116767. photochemical
  116768. rearrangements
  116769. fragmentations
  116770. benzene
  116771. photochemical
  116772. rearrangements
  116773. involving
  116774. three
  116775. membered
  116776. rings
  116777. photochemical
  116778. rearrangements
  116779. conjugated
  116780. cyclic
  116781. dienones
  116782. photochemical
  116783. rearrangements
  116784. enones
  116785. photochemical
  116786. rearrangements
  116787. five-membered
  116788. heterocycles
  116789. photochemical
  116790. rearrangements
  116791. trienes
  116792. photochemical
  116793. closure
  116794. 1-tosyl-12-diaryleth
  116795. photochemical
  116796. expansion
  116797. cyclic
  116798. ketones
  116799. cyclic
  116800. photochemical
  116801. electron
  116802. heterocyclization
  116803. reactions
  116804. photochemical
  116805. strategies
  116806. construction
  116807. polycyclic
  116808. photochemical
  116809. synthesis
  116810. photochemical-synthe
  116811. photochemically
  116812. photochemically
  116813. induced
  116814. activation
  116815. ligand
  116816. trans
  116817. photochemicnl
  116818. photochemis
  116819. photochemis
  116820. alkenes
  116821. alkynes
  116822. related
  116823. compounds
  116824. photochemistry
  116825. photochemical
  116826. rearrangements
  116827. fragmentations
  116828. benzene
  116829. photochemical
  116830. contraction
  116831. dihydro
  116832. benzothiazines@
  116833. photochemistry
  116834. photochemistry
  116835. furanones@
  116836. photochroism
  116837. photocycloadditions@
  116838. photoinduced
  116839. photoinduced
  116840. hydrogen
  116841. abstraction
  116842. carbonyl
  116843. compounds@
  116844. photophysical
  116845. phototransposition
  116846. chemistry
  116847. phenylisothiazoles
  116848. pheny@
  116849. physical
  116850. piatak
  116851. wicha
  116852. various
  116853. approaches
  116854. construction
  116855. pictorial@
  116856. pigments
  116857. stanley
  116858. carbonyl
  116859. methylenation
  116860. alkylidenation
  116861. piperidines
  116862. ammonium
  116863. ylide
  116864. shifts
  116865. concise
  116866. enantiose@
  116867. platform@
  116868. platz
  116869. plueddemann
  116870. edwin
  116871. silane
  116872. coupling
  116873. reagents
  116874. plenum
  116875. podocarpic@
  116876. polarized
  116877. hydroxybutanoates
  116878. fifth
  116879. class
  116880. physiologically
  116881. impo@
  116882. polyanions@
  116883. polycyclic
  116884. aromatic
  116885. hydrocarbons@
  116886. sulfides
  116887. throu@
  116888. power
  116889. photochemistry
  116890. photochemistry
  116891. photophysics
  116892. onium
  116893. salts
  116894. photochemistry
  116895. organized
  116896. confining
  116897. media
  116898. model
  116899. photochemistry
  116900. treatment
  116901. cancer
  116902. photochemistry
  116903. furanones
  116904. photochemistry
  116905. 2-dialkylamino-14-na
  116906. photochemistry
  116907. dimethyl
  116908. tetramethyl
  116909. photochemistry
  116910. alkyl
  116911. alkylidene
  116912. alkylidyne
  116913. complexes
  116914. photochemistry
  116915. aromatic
  116916. compounds
  116917. photochemistry
  116918. halides
  116919. related
  116920. compound
  116921. photochemistry
  116922. carboxylic
  116923. derivatives
  116924. photochemistry
  116925. cyclopropanes
  116926. photochemistry
  116927. allenyl
  116928. substituted
  116929. conjugated
  116930. alkyliden
  116931. photochemistry
  116932. hydroxamic
  116933. acids
  116934. derivatives
  116935. photochemistry
  116936. organic
  116937. bichromophoric
  116938. molecules
  116939. photochemistry
  116940. oxygen
  116941. sulphur
  116942. containing
  116943. heterocycles
  116944. photochemistry
  116945. phenyl
  116946. azide
  116947. photochemistry
  116948. phosphate
  116949. esters
  116950. photochemistry
  116951. radicals
  116952. biradicals
  116953. photochemistry
  116954. reaction
  116955. intermediates
  116956. photochemistry
  116957. simple
  116958. olefins
  116959. chemistry
  116960. electronic
  116961. photochemistry
  116962. carbon-nitrogen
  116963. double
  116964. photochlorination
  116965. photochroism
  116966. photochroism
  116967. photochromes
  116968. photochromic
  116969. photochromism
  116970. photocleavage
  116971. photocontrol
  116972. photocyclization
  116973. photocyclizations
  116974. photocyclizations
  116975. intramolecular
  116976. photocycloadditions
  116977. photocycloaddit
  116978. photocycloaddition
  116979. photocycloaddition
  116980. benzothiazole
  116981. thiones
  116982. alkenes
  116983. photocycloaddition/f
  116984. photocycloadditions
  116985. control
  116986. energy
  116987. electron
  116988. transfer
  116989. photodecomposition
  116990. photodimerization
  116991. photodissociation
  116992. photoelectron
  116993. photoenolisation
  116994. photoexcited
  116995. photoexited
  116996. photoextrusion
  116997. photofunctional
  116998. photogenerated
  116999. photogeneration
  117000. photography
  117001. photoinduced
  117002. photoinduced
  117003. photoinduced
  117004. charge
  117005. separation
  117006. twisted
  117007. intramolecular
  117008. photoinduced
  117009. charge
  117010. transfer
  117011. processes
  117012. semiconductor
  117013. photoinduced
  117014. electron
  117015. transfer
  117016. photoinduced
  117017. electron
  117018. transfer
  117019. multiple
  117020. states
  117021. mechanism
  117022. photoinduced
  117023. electron
  117024. transfer
  117025. employing
  117026. organic
  117027. anions
  117028. photoinduced
  117029. electron
  117030. transfer
  117031. flexible
  117032. biaryl
  117033. donor
  117034. photoinduced
  117035. electron
  117036. transfer
  117037. carbanions
  117038. carbocation
  117039. photoinduced
  117040. electron
  117041. transfer
  117042. cleavage
  117043. reactions
  117044. photoinduced
  117045. electron
  117046. transfer
  117047. organic
  117048. synthesis
  117049. photoinduced
  117050. electron-transfer
  117051. reactions
  117052. photoinduced
  117053. hydrogen
  117054. abstraction
  117055. carbonyl
  117056. compounds
  117057. photoinduced
  117058. molecular
  117059. transformations
  117060. total
  117061. synth
  117062. photoinduced
  117063. vinylcyclopropane
  117064. cyclopentene
  117065. rearrangement
  117066. photoinitiated
  117067. photoinitiated
  117068. free-radical
  117069. chain
  117070. reactions
  117071. photoinitiation
  117072. photoisomerization
  117073. photoisomerization
  117074. dynamics
  117075. stilbenes
  117076. photoisomerizations
  117077. photoluminescence
  117078. photolysis
  117079. photolysis
  117080. carbonyl
  117081. compounds
  117082. photolytic
  117083. photolytic
  117084. generation
  117085. acylnitrenium
  117086. under
  117087. neutral
  117088. photolytic
  117089. rearrangement
  117090. isobutyl
  117091. oxazaspiro
  117092. photon
  117093. photooxidation
  117094. photooxidation
  117095. ketoester
  117096. photooxygenation
  117097. photooxygenations
  117098. photophysical
  117099. photophysical
  117100. photophysical
  117101. photochemical
  117102. processes
  117103. micellar
  117104. system
  117105. photophysical
  117106. photochemical
  117107. properties
  117108. fullerenes
  117109. photophysics
  117110. photoprocesses
  117111. photoreaction
  117112. photoreactions
  117113. photoreactions
  117114. fullerene
  117115. photocycloaddition
  117116. photoreactivity
  117117. photorearrangement
  117118. photorearrangements
  117119. photorearrangements
  117120. biradicals
  117121. simple
  117122. carbonyl
  117123. compou
  117124. photoremovable
  117125. photosensitive
  117126. photosensitization
  117127. photosensitization
  117128. organic
  117129. synthesis
  117130. photosensitized
  117131. photosensitizer
  117132. photosolvolyses
  117133. photosubstitution
  117134. photosubstitution
  117135. reactions
  117136. aromatic
  117137. compounds
  117138. photosubstitutions
  117139. photosynthesis
  117140. photosynthetic
  117141. phototherapy
  117142. phototransposition
  117143. phototransposition
  117144. chemistry
  117145. phenylisothiazoles
  117146. pheny
  117147. photoxidation
  117148. phthalazin
  117149. phthalazines
  117150. phthalimide
  117151. phthalimides
  117152. phthalimidesulfenyl
  117153. phthalimidesulfenyl
  117154. chloride
  117155. synthesis
  117156. substituted
  117157. phthalocyanine
  117158. phthalocyanines
  117159. phthaloyl
  117160. phyaical
  117161. phyllanthocin
  117162. physical
  117163. physical
  117164. physical
  117165. chemical
  117166. properties
  117167. singlet
  117168. molecular
  117169. oxygen
  117170. physicochemical
  117171. physics
  117172. physiological
  117173. physiologically
  117174. physiology
  117175. physostigmine
  117176. phytoalexine
  117177. phytoalexins
  117178. phytochemistry
  117179. phytochemistry
  117180. acetylenes
  117181. related
  117182. compounds
  117183. phytosterol
  117184. phytoxanthones
  117185. allyl
  117186. nickel
  117187. halides
  117188. selective
  117189. reagents
  117190. organic
  117191. allylnickel
  117192. halides
  117193. selective
  117194. reagents
  117195. organic
  117196. pi-complexes
  117197. pi-electronic
  117198. pi-rearrangements
  117199. piacenti
  117200. piancatelli
  117201. piano
  117202. piano-stool
  117203. piatak
  117204. piatak
  117205. wicha
  117206. various
  117207. approaches
  117208. construction
  117209. piccirilli
  117210. pickart
  117211. picken
  117212. pickenhagen
  117213. picoline
  117214. picosecond
  117215. picrotoxanes
  117216. pictet
  117217. pictet-spengler
  117218. pierce
  117219. piere
  117220. pierfrancesco
  117221. pierini
  117222. pierluigi
  117223. piero
  117224. pierre
  117225. piers
  117226. piers
  117227. warren
  117228. shapiro
  117229. pamela
  117230. bunel
  117231. emilio
  117232. bercaw
  117233. pietek
  117234. pietra
  117235. pietra
  117236. revival
  117237. troponoid
  117238. chemistry
  117239. 197912132
  117240. accounts
  117241. pietro
  117242. pietrusiewicz
  117243. piettre
  117244. piezochromism
  117245. liver
  117246. esterase
  117247. catalyzed
  117248. hydrolysis
  117249. substrate
  117250. specificit
  117251. pigman
  117252. pigman
  117253. horton
  117254. wander
  117255. carbohydrates
  117256. chemistry
  117257. pigment
  117258. pigments
  117259. pigments
  117260. pigments
  117261. visual
  117262. differentiation
  117263. enantiomers
  117264. crown
  117265. piiar
  117266. sweigart
  117267. single
  117268. double
  117269. nucleophilic
  117270. additio
  117271. pikul
  117272. pillai
  117273. pillai
  117274. photoremovable
  117275. protecting
  117276. groups
  117277. organic
  117278. pimentel
  117279. pinacol
  117280. pinacol
  117281. coupling
  117282. reactions
  117283. pinacol
  117284. cross
  117285. coupling
  117286. alkoxycarbonyl
  117287. amino
  117288. aldehydes
  117289. pinacol
  117290. rearrangement
  117291. molecular
  117292. sieves
  117293. pinacolone
  117294. pinacols
  117295. pinder
  117296. pinder
  117297. azetidine
  117298. pyrrole
  117299. pyrrolidine
  117300. piperidine
  117301. pinder
  117302. chemistry
  117303. eremophilane
  117304. related
  117305. sesquiterpe
  117306. pinder
  117307. pyrrole
  117308. pyrrolidine
  117309. piperidine
  117310. azepine
  117311. alkalo
  117312. pinder
  117313. hydrogenolysis
  117314. organic
  117315. halides
  117316. pindur
  117317. pindur
  117318. gundula
  117319. christian
  117320. acceleration
  117321. stanley
  117322. carbonyl
  117323. methylenation
  117324. alkylidenation
  117325. pinene
  117326. pines
  117327. pines
  117328. chemistry
  117329. catalytic
  117330. hydrocarbon
  117331. conversions
  117332. pinhey
  117333. pinhey
  117334. organolead
  117335. tricarboxylates
  117336. reagents
  117337. pinnick
  117338. mulhaupt
  117339. stereospecific
  117340. polymerization
  117341. propylene
  117342. pinsker
  117343. pioneer
  117344. piotr
  117345. piozzi
  117346. piozzi
  117347. diterpenoids
  117348. teucrium
  117349. species
  117350. piozzi
  117351. franco
  117352. f'urther
  117353. researches
  117354. furocle
  117355. rodanes
  117356. pipecolic
  117357. pipecoline
  117358. piper
  117359. piperazine-25-diones
  117360. piperazine-25-diones
  117361. related
  117362. lactim
  117363. ethers
  117364. piperazinediones
  117365. piperazinomycin
  117366. piperidine
  117367. piperidine-4
  117368. piperidine4
  117369. piperidines
  117370. piperidines
  117371. ammonium
  117372. ylide
  117373. shifts
  117374. concise
  117375. enantiose
  117376. piperidinones
  117377. piperidones
  117378. piras
  117379. pirkle
  117380. pirozhkov
  117381. pis'man
  117382. pisulina
  117383. pittman
  117384. pizey
  117385. pizzo
  117386. place
  117387. planar
  117388. planar-tetracoordina
  117389. planarizing
  117390. planning
  117391. planococcyl
  117392. plant
  117393. plants
  117394. plasma
  117395. platinum-catalyzed
  117396. plato
  117397. plato's
  117398. plato's
  117399. solid
  117400. dodecahedrane
  117401. story
  117402. platonov
  117403. platz
  117404. platz
  117405. platz
  117406. matthew
  117407. leyva
  117408. elisa
  117409. haider
  117410. selected
  117411. topics
  117412. playground
  117413. pleiadienes
  117414. pleiadienes
  117415. acepleiadienes
  117416. pleiss
  117417. pleixats
  117418. plenary
  117419. plenum
  117420. plesek
  117421. plesek
  117422. jaromir
  117423. potential
  117424. applications
  117425. boron
  117426. cluster
  117427. plesnicar
  117428. plesnicar
  117429. oxidations
  117430. peroxy
  117431. acids
  117432. other
  117433. peroxides
  117434. pleuromutilin
  117435. plications
  117436. plisko
  117437. plisko
  117438. nud'ga
  117439. danilov
  117440. chitin
  117441. chemical
  117442. ploegh
  117443. plotnikov
  117444. plotnikov
  117445. ovchinnikov
  117446. photochemical
  117447. radiatio
  117448. plueddemann
  117449. plueddemann
  117450. edwin
  117451. silane
  117452. coupling
  117453. reagents
  117454. plenum
  117455. po-activated
  117456. pochapsky
  117457. pochinok
  117458. pocket
  117459. podophyllotoxin
  117460. podraza
  117461. pogorelyi
  117462. pohlmann
  117463. point
  117464. points
  117465. poirier
  117466. poisel
  117467. poison
  117468. poisons
  117469. poland
  117470. polar
  117471. polar
  117472. allyl
  117473. organometallics
  117474. intermediates
  117475. polar
  117476. cycloadditions
  117477. polar
  117478. effects
  117479. organic
  117480. reactions
  117481. polar
  117482. rearrangements
  117483. polar-carbanions
  117484. polar-carbanions
  117485. organometal
  117486. compounds
  117487. theoretical
  117488. introduct
  117489. polarimetric
  117490. polarimetric
  117491. detection
  117492. highperformance
  117493. liquid
  117494. chromatogra
  117495. polarimetry
  117496. polarity
  117497. polarity
  117498. control
  117499. synthesis
  117500. polarizability
  117501. polarization
  117502. polarized
  117503. polarized
  117504. polarography
  117505. polezhaeva
  117506. rinaldo
  117507. monocyclopentadienyl
  117508. halide
  117509. complexes
  117510. policyclic
  117511. polikarpov
  117512. polimbetova
  117513. poling
  117514. polisaccharides
  117515. polishchuk
  117516. politech
  117517. polivin
  117518. pollack
  117519. pollard
  117520. pollard
  117521. renee
  117522. peter
  117523. synthetic
  117524. applications
  117525. diaryl
  117526. pollini
  117527. poloni
  117528. polonovski
  117529. polonovski
  117530. pummerer-type
  117531. reactions
  117532. reaction
  117533. polumbrik
  117534. polumbrik
  117535. advances
  117536. chemistry
  117537. verdazyl
  117538. radicals
  117539. hydroxybutanoates
  117540. fifth
  117541. class
  117542. physiologically
  117543. pyrazolyl
  117544. borate
  117545. complexes
  117546. poly-halogen
  117547. polyacene
  117548. polyacetylenes
  117549. polyaddition
  117550. polyalkali
  117551. polyalkalimetal
  117552. polyalkynes
  117553. polyallenes
  117554. polyamine
  117555. polyamines
  117556. polyanions
  117557. polyaromatic
  117558. polyarylmethyl
  117559. polyatomic
  117560. polyaza
  117561. polyazaphenanthrenes
  117562. polyazaphosphorus
  117563. polyazaphosphorus
  117564. macrocycles
  117565. synthesis
  117566. reactivity
  117567. complexat
  117568. polyborane
  117569. polybromo
  117570. polycalicenyls
  117571. polycarbanions
  117572. polycarbocations
  117573. polycarbocyclic]
  117574. polycarbodiimides
  117575. polycarbonates
  117576. polychlorinated
  117577. polychloroalkanes
  117578. polychromophoric
  117579. polycondensation
  117580. polycoordinated
  117581. polycycle
  117582. polycycles
  117583. polycyclic^
  117584. polycyclic
  117585. anions
  117586. doubly
  117587. highly
  117588. charged
  117589. conjugated
  117590. polycyclic
  117591. aromatic
  117592. hydrocarbons
  117593. polycyclic
  117594. aromatic
  117595. nitrogen
  117596. cations
  117597. polycyclic
  117598. compounds
  117599. intermediates
  117600. organic
  117601. synthe
  117602. polycyclic
  117603. molecules
  117604. useful
  117605. intermediates
  117606. organic
  117607. polycyclics
  117608. polycyclization
  117609. polycyclopentanoid
  117610. polydecker
  117611. polydentate
  117612. polyelementorganic
  117613. polyenals
  117614. polyene
  117615. polyene
  117616. cyclizations
  117617. polyenes
  117618. polyenoic
  117619. polyepoxide
  117620. polyepoxides
  117621. polyether
  117622. lyethers
  117623. polyfluorinated
  117624. polyfluorinated
  117625. 213-benzothia
  117626. selena
  117627. diazoles
  117628. heuristic
  117629. polyfluorinated
  117630. troxides
  117631. polyfluoro
  117632. polyfluoroalkylsulfe
  117633. polyfluoroalkylsulfe
  117634. chlorides
  117635. polyfluoroarenes
  117636. polyfluoroarenes
  117637. polyfluoroaromatic
  117638. polyfluorobenzenes
  117639. polyfluorocompounds
  117640. polyfluoroheteroarom
  117641. polyfluoroketones
  117642. polyfunctional
  117643. polyfunctionalized
  117644. polyfunctionally
  117645. polyhalide
  117646. polyhalides
  117647. polyhalo
  117648. polyhalocompounds
  117649. polyhalogenoalkanes
  117650. polyhalomethanes
  117651. polyhedral
  117652. polyhedron
  117653. polyhedron
  117654. kinetics
  117655. mechanism
  117656. substituti
  117657. polyhedron
  117658. chiral
  117659. acetals
  117660. asymmetric
  117661. synthesis
  117662. polyhedron
  117663. coordinately
  117664. unsaturated
  117665. tripalladium
  117666. polyheteroarylenes
  117667. polyheterocyclisatio
  117668. polyhydroxy
  117669. polyhydroxylated
  117670. polyhydroxysteroids
  117671. polyketide
  117672. polyketides
  117673. polyketones
  117674. polylithiated
  117675. polymer
  117676. polymer
  117677. polymer
  117678. supported
  117679. catalysts
  117680. polymer
  117681. supported
  117682. reactions
  117683. organic
  117684. synthesis
  117685. polymeric
  117686. polymeric
  117687. organotellurium
  117688. compounds
  117689. polymerisation
  117690. polymerization
  117691. polymers
  117692. polymers
  117693. organic
  117694. synthesis
  117695. review
  117696. polymers
  117697. reagents
  117698. organic
  117699. synthesis
  117700. polymers
  117701. heteroatom
  117702. chain
  117703. polymers
  117704. c-main
  117705. chains
  117706. polymerization
  117707. polymers
  117708. purely
  117709. mostly
  117710. inorganic
  117711. polymer
  117712. chain
  117713. polymetalations
  117714. polymethine
  117715. polymethyl
  117716. polynitrogen
  117717. polynomial
  117718. polynorbornyl
  117719. polynuclear
  117720. polynuclear
  117721. aromatic
  117722. compounds
  117723. polynucleotides
  117724. polynuelear
  117725. polyol
  117726. polyolefin
  117727. polyolefinic
  117728. polyols
  117729. polyorgano
  117730. polyoxa
  117731. polyoxa
  117732. polythia
  117733. polyaza
  117734. six-membered
  117735. systems
  117736. polyoxins
  117737. xometalate
  117738. polyoxometalate
  117739. chemistry
  117740. theme
  117741. dimensions
  117742. polyoxometallate
  117743. polyoxygenated
  117744. polypeptide
  117745. polypeptides
  117746. polyphenols
  117747. polyphosphane
  117748. polyphosphanes
  117749. polyphosphine
  117750. polyphosphorus
  117751. polyprenoid
  117752. polypropionate
  117753. polypropionate-deriv
  117754. polyquinane
  117755. polyquinanes
  117756. polyquinenes
  117757. polyradicals
  117758. polyreactions
  117759. polysaccharide
  117760. polysaccharides
  117761. polysaccharides
  117762. polysubstituted
  117763. polysulfanes
  117764. polysulfides
  117765. polysulfur
  117766. polysulfur-nitrogen
  117767. polysulfur-nitrogen
  117768. heterocyclic
  117769. chemistry
  117770. polysynthons
  117771. polyterpenoids
  117772. polythia
  117773. polytopal
  117774. polytopic
  117775. polyunsaturated
  117776. polyvalent
  117777. polyvalent
  117778. iodine
  117779. compounds
  117780. organic
  117781. synthesis
  117782. polyynes
  117783. pomeranz
  117784. pomeranz-fritsch
  117785. pommer
  117786. ponnamperuma
  117787. ponnamperuma
  117788. cyril
  117789. macdermott
  117790. alexandra
  117791. cosmic
  117792. asymmetry
  117793. ponndorf
  117794. ponomarenko
  117795. ponomarev
  117796. ponomareva
  117797. pool-derived
  117798. poonam
  117799. poonia
  117800. poonia
  117801. multidentate
  117802. macromolecules
  117803. principles
  117804. complex
  117805. popkov
  117806. popov
  117807. popova
  117808. developments
  117809. chemistry
  117810. reissert
  117811. compounds
  117812. poppe
  117813. poppe
  117814. novak
  117815. selective
  117816. biocatalysis
  117817. synthetic
  117818. approach
  117819. porai
  117820. poranski
  117821. porantheridine
  117822. porifera
  117823. porphyrin
  117824. porphyrin-quinone
  117825. porphyrin-quinone
  117826. compounds
  117827. synthetic
  117828. models
  117829. react
  117830. porphyrinoids
  117831. porphyrins
  117832. porphyrins
  117833. corrins
  117834. phthalocyanines
  117835. porschnev
  117836. porshnev
  117837. porta
  117838. porter
  117839. porter
  117840. giese
  117841. bernd
  117842. curran
  117843. dennis
  117844. acyclic
  117845. stereochemi
  117846. portion
  117847. portions
  117848. portoghese
  117849. portoghese
  117850. stereoisomeric
  117851. ligands
  117852. opioid
  117853. receptor
  117854. porwoll
  117855. position
  117856. positional
  117857. positions
  117858. positive
  117859. positively
  117860. positively
  117861. posner
  117862. posner
  117863. introduction
  117864. synthesis
  117865. using
  117866. organocopper
  117867. posner
  117868. organic
  117869. reactions
  117870. alumina
  117871. surfaces
  117872. pospichal
  117873. pospisil
  117874. christopher
  117875. schreiber
  117876. stuart
  117877. directional
  117878. chain
  117879. possessing
  117880. possibilities
  117881. possible
  117882. possible
  117883. surface
  117884. intermediates
  117885. alkane
  117886. reactions
  117887. metall
  117888. modification
  117889. peptoid
  117890. chains
  117891. cycloaddition
  117892. postavskii
  117893. postawka
  117894. postovskii
  117895. potassium
  117896. potassium
  117897. monopersulfate
  117898. another
  117899. primary
  117900. oxidant
  117901. potassium
  117902. t-butoxide
  117903. synthesis
  117904. potassium
  117905. triisopropylsilaneth
  117906. vinyl
  117907. sulfides
  117908. throu
  117909. potency
  117910. potent
  117911. potential
  117912. potential
  117913. applications
  117914. enzyme-mediated
  117915. transesterificatio
  117916. potential
  117917. applications
  117918. boron
  117919. cluster
  117920. compounds
  117921. potentialities
  117922. potentially
  117923. potentials
  117924. potier
  117925. potier
  117926. pierre
  117927. search
  117928. discovery
  117929. antitumor
  117930. compound
  117931. potts
  117932. potucek
  117933. poulson
  117934. poulter
  117935. poulter
  117936. rilling
  117937. prenyl
  117938. transfer
  117939. reaction
  117940. enzymat
  117941. poundsj
  117942. poupat
  117943. poveda
  117944. powder
  117945. powders
  117946. powell
  117947. power
  117948. power
  117949. powerful
  117950. powers
  117951. poylcyclic
  117952. pozharskii
  117953. pozharskii
  117954. simonov
  117955. doron'kin
  117956. advances
  117957. pozzi
  117958. pr4nv
  117959. practica
  117960. practica
  117961. useful
  117962. methods
  117963. enantioselective
  117964. reducti
  117965. practical
  117966. practical
  117967. catalyst
  117968. cyclic
  117969. metathesis
  117970. synthesis
  117971. functi
  117972. practical
  117973. method
  117974. preparation
  117975. nitrate
  117976. esters
  117977. practical
  117978. photochemistry
  117979. general
  117980. considerations
  117981. practical
  117982. photochemistry
  117983. scale
  117984. practical
  117985. review
  117986. lanthanide
  117987. shift
  117988. reagents
  117989. practical
  117990. stereocontrolled
  117991. synthesis
  117992. functionalized
  117993. practical
  117994. synthesis
  117995. palladium
  117996. trifluoromethanesulf
  117997. practice
  117998. pradeep
  117999. pradhan
  118000. praetical
  118001. praetice
  118002. pragmatism
  118003. prakach
  118004. prakash
  118005. practica
  118006. useful
  118007. methods
  118008. enantioselective
  118009. reducti@
  118010. prakash
  118011. saini
  118012. neena
  118013. sharma
  118014. pawan
  118015. hydroxy
  118016. tosyloxy
  118017. precursor-directed@
  118018. preferences@
  118019. preferred@
  118020. preparation
  118021. preparation
  118022. properties
  118023. reactions
  118024. applications
  118025. preparation
  118026. steric
  118027. structure
  118028. condensed
  118029. skeleton
  118030. satur@
  118031. preparation
  118032. carbolines@
  118033. preparation
  118034. substituted
  118035. methyl
  118036. oxadiazoles
  118037. preparation
  118038. aromatic
  118039. fluorine
  118040. compounds
  118041. diazonium
  118042. preparation
  118043. macromol
  118044. materials
  118045. reactions
  118046. macro@
  118047. preparation
  118048. enantiomers
  118049. compounds
  118050. containing
  118051. chira@
  118052. preparative
  118053. acetylenic
  118054. chemistry@
  118055. presentation
  118056. press
  118057. primer
  118058. probes
  118059. procedures@
  118060. processes
  118061. processing@
  118062. product
  118063. product
  118064. stability
  118065. kinetically-controll
  118066. organic
  118067. reactions@
  118068. products
  118069. thesis
  118070. ene-diyne
  118071. antica@
  118072. practica
  118073. useful
  118074. methods
  118075. enantioselective
  118076. reducti@
  118077. preparation
  118078. five-membered
  118079. nitrogen
  118080. heterocycles
  118081. three@
  118082. products1991@
  118083. promoter@
  118084. protective
  118085. group
  118086. strategies
  118087. synthesis
  118088. functionaliz@
  118089. proton-ionizable@
  118090. pyrazoles
  118091. fused
  118092. six-membered
  118093. heterocyclic
  118094. rings@
  118095. radical
  118096. chemistry
  118097. associated
  118098. thiocarbonyl
  118099. group
  118100. reaction
  118101. halodiaziridines
  118102. electron
  118103. transfer
  118104. readily
  118105. available
  118106. chromenone
  118107. receptors
  118108. carboxylates@
  118109. rearrangements@
  118110. recent
  118111. advances
  118112. chemistry
  118113. chlorosulphonyl
  118114. isocyanat@
  118115. reduction
  118116. inorganic
  118117. reducing
  118118. agents
  118119. metal
  118120. salts@
  118121. enantiom@
  118122. route
  118123. ruthenium-catalyzed
  118124. oxidative
  118125. transformations
  118126. alcohols@
  118127. schneider
  118128. frontiers
  118129. supramolecular
  118130. organic
  118131. sener
  118132. recent
  118133. results
  118134. search
  118135. bioactive
  118136. compounds@
  118137. shono
  118138. tatsuya
  118139. electroorganic
  118140. synthesis
  118141. academic
  118142. london
  118143. prakash
  118144. saini
  118145. neena
  118146. sharma
  118147. pawan
  118148. hydroxy
  118149. tosyloxy
  118150. prakash
  118151. saini
  118152. sharma
  118153. hypervalent
  118154. iodine
  118155. reagents
  118156. prakash
  118157. saini
  118158. neena
  118159. sharma
  118160. pawan
  118161. hypervalent
  118162. iodine
  118163. prakash
  118164. singh
  118165. iodobenzene
  118166. diacetate
  118167. related
  118168. prasad
  118169. prasanna
  118170. prassd
  118171. prassides
  118172. pratt
  118173. preassembled
  118174. prebiological
  118175. prebiotic
  118176. precautions
  118177. preconditions
  118178. precursor
  118179. rsor-directed
  118180. precursors
  118181. predicting
  118182. predicting
  118183. forbidden
  118184. allowed
  118185. cycloaddition
  118186. reactions
  118187. prediction
  118188. predictive
  118189. predvoditelev
  118190. preface
  118191. preference
  118192. preferences
  118193. preferential
  118194. preferential
  118195. hydrogenation
  118196. aldehydes
  118197. ketones
  118198. synthesis
  118199. preformed
  118200. pregna
  118201. preininger
  118202. preliminary
  118203. prelog
  118204. prelog
  118205. vladimir
  118206. semesters
  118207. studies
  118208. chemistry
  118209. prelog-djerasi
  118210. prelog-djerassi
  118211. prelog-djerassi
  118212. lactonic
  118213. target
  118214. design
  118215. develo
  118216. premila
  118217. prentice
  118218. prenyl
  118219. prenylated
  118220. prenylation
  118221. prenylflavonoids
  118222. prenylphenols
  118223. prepara
  118224. preparartion
  118225. preparati
  118226. preparati
  118227. reactivity
  118228. alpha-zirconocenyl
  118229. thioethers
  118230. preparatio
  118231. preparatio
  118232. alpha
  118233. beta-unsaturated
  118234. carbonyl
  118235. compounds
  118236. preparationP
  118237. preparation
  118238. preparation
  118239. preparation
  118240. chemistry
  118241. stable
  118242. azidoiodinanes
  118243. 1-azido-3
  118244. preparation
  118245. cycloaddition
  118246. reactions
  118247. silylated
  118248. thiophe
  118249. preparation
  118250. diels-alder
  118251. reactions
  118252. hetero-substituted
  118253. preparation
  118254. intramolecular
  118255. radical
  118256. cyclization
  118257. preparation
  118258. photolysis
  118259. heterosubstituted
  118260. alkeny
  118261. preparation
  118262. properties
  118263. chiral
  118264. fluoroorganic
  118265. compounds
  118266. preparation
  118267. properties
  118268. organosilicon
  118269. peroxides
  118270. preparation
  118271. properties
  118272. reactions
  118273. applications
  118274. preparation
  118275. pyrolysis
  118276. cyclic
  118277. sulfones
  118278. preparation
  118279. reactions
  118280. tert-butyldimethylsi
  118281. 3-lithio
  118282. preparation
  118283. reactions
  118284. cyclic
  118285. alpha
  118286. nitroketones
  118287. preparation
  118288. reactions
  118289. cyclic
  118290. alpha-nitroketones
  118291. preparation
  118292. reactions
  118293. zomalonic
  118294. esters
  118295. preparation
  118296. reactions
  118297. diorganozincs
  118298. dienic
  118299. silyl
  118300. preparation
  118301. reactions
  118302. indolin
  118303. preparation
  118304. reactions
  118305. indolin
  118306. review
  118307. preparation
  118308. reactions
  118309. indolin-2
  118310. preparation
  118311. reactions
  118312. polyfunctional
  118313. organozinc
  118314. reage
  118315. preparation
  118316. reactivity
  118317. b-nitrogen
  118318. functionalized
  118319. preparation
  118320. reduction
  118321. camphor
  118322. imines
  118323. preparation
  118324. applications
  118325. functionalized
  118326. organo-l
  118327. preparation
  118328. spectroscopic
  118329. properties
  118330. spirocyclic
  118331. preparation
  118332. steric
  118333. structure
  118334. condensed
  118335. skeleton
  118336. satur
  118337. preparation
  118338. synthetic
  118339. applications
  118340. cyano
  118341. compounds
  118342. preparation
  118343. symmetric
  118344. phospholanes
  118345. productio
  118346. preparation
  118347. organic
  118348. synthesis
  118349. organolithium
  118350. preparation
  118351. iodoalkyl
  118352. ylides
  118353. preparation
  118354. grignard
  118355. reagents
  118356. group
  118357. organo
  118358. preparation
  118359. highly
  118360. hindered
  118361. amines
  118362. bases
  118363. preparation
  118364. organoboranes
  118365. organic
  118366. synthesis
  118367. preparation
  118368. organosilicon
  118369. compounds
  118370. organic
  118371. preparation
  118372. organothallium
  118373. compounds
  118374. organ
  118375. preparation
  118376. construction
  118377. aromatic
  118378. systems
  118379. non-aro
  118380. preparation
  118381. construction
  118382. polycyclic
  118383. aromatic
  118384. hydrocarb
  118385. preparation
  118386. characterization
  118387. synthetic
  118388. potential
  118389. preparation
  118390. aromatic
  118391. compounds
  118392. introduction
  118393. elimi
  118394. preparation
  118395. aromatic
  118396. compounds
  118397. substitution
  118398. preparation
  118399. carbolines
  118400. preparation
  118401. 1-cyclopropylideneal
  118402. reagents
  118403. preparation
  118404. 13-dizinc
  118405. compounds
  118406. boron-zinc
  118407. exchange
  118408. preparation
  118409. hexahydrotriazines
  118410. triazines
  118411. deriva
  118412. preparation
  118413. substituted
  118414. hydroxy
  118415. methylfurans
  118416. preparation
  118417. dihydro
  118418. oxadiazino
  118419. preparation
  118420. benzoxetes
  118421. photoinduced
  118422. cycloadditi
  118423. preparation
  118424. bromo
  118425. methylfuran
  118426. bromo
  118427. methylfur
  118428. preparation
  118429. 3-thienylzinc
  118430. magnesium
  118431. halide
  118432. oxidat
  118433. preparation
  118434. aldehydes
  118435. degradation
  118436. preparation
  118437. aldehydes
  118438. formation
  118439. reactions
  118440. preparation
  118441. aldehydes
  118442. oxidation
  118443. preparation
  118444. aldehydes
  118445. rearrangement
  118446. conservation
  118447. preparation
  118448. aldehydes
  118449. reduction
  118450. preparation
  118451. aldehydes
  118452. aldehyde
  118453. derivatives
  118454. preparation
  118455. aldehydes
  118456. other
  118457. aldehydes
  118458. conservat
  118459. preparation
  118460. aromatic
  118461. fluorine
  118462. compounds
  118463. diazonium
  118464. preparation
  118465. aromatic
  118466. fluorine
  118467. compounds
  118468. diazoniunn
  118469. preparation
  118470. arylthio
  118471. iodobenzene
  118472. reaction
  118473. preparation
  118474. carbocyclic
  118475. heterocyclic
  118476. compounds
  118477. preparation
  118478. chloro
  118479. nitrocompounds
  118480. olefins
  118481. preparation
  118482. conjugated
  118483. dienes
  118484. enynes
  118485. organo
  118486. coppe
  118487. preparation
  118488. diamino
  118489. ethers
  118490. polyamines
  118491. preparation
  118492. epoxides
  118493. oxidative
  118494. decarbonylation
  118495. preparation
  118496. fluorinated
  118497. ketones
  118498. preparation
  118499. unsaturated
  118500. acids
  118501. conjugate
  118502. addition
  118503. preparation
  118504. highly
  118505. reactive
  118506. metal
  118507. powders
  118508. their
  118509. preparation
  118510. homochiral
  118511. organic
  118512. compounds
  118513. preparation
  118514. ketenes
  118515. ketene
  118516. dimers
  118517. preparation
  118518. ketenes
  118519. ketene
  118520. dimers
  118521. hanford
  118522. preparation
  118523. ketones
  118524. reaction
  118525. organolithium
  118526. preparation
  118527. omolecular
  118528. materials
  118529. polyreactions
  118530. preparation
  118531. macromol
  118532. materials
  118533. reactions
  118534. macro
  118535. preparation
  118536. macromolecular
  118537. materials
  118538. combination
  118539. preparation
  118540. diprotected
  118541. allylic
  118542. amines
  118543. palladium
  118544. preparation
  118545. substituted
  118546. succinimides
  118547. preparation
  118548. tosylaldimines
  118549. preparation
  118550. disubstituted
  118551. oxazoles
  118552. preparation
  118553. polyfunctional
  118554. diorganozincs
  118555. using
  118556. preparation
  118557. nucleoside
  118558. phosphorothioates
  118559. phosphorodithioa
  118560. preparation
  118561. opium
  118562. alkaloids
  118563. palladium
  118564. catalyzed
  118565. preparation
  118566. organo-pi-metal
  118567. compounds
  118568. preparation
  118569. organometallic
  118570. compounds
  118571. highly
  118572. reactive
  118573. preparation
  118574. organosilicon
  118575. compounds
  118576. preparation
  118577. pyrroles
  118578. ketoximes
  118579. acetylenes
  118580. preparation
  118581. scalemic
  118582. p-chiral
  118583. phosphines
  118584. their
  118585. deriva
  118586. preparation
  118587. selectively
  118588. alkylated
  118589. saccharides
  118590. syntheti
  118591. preparation
  118592. tetrahydrobenz
  118593. indoles
  118594. tetralones
  118595. preparation
  118596. enantiomers
  118597. compounds
  118598. containing
  118599. chira
  118600. preparation
  118601. thiocarbamoyl
  118602. chlorides
  118603. preparation
  118604. thiophene
  118605. oligomers
  118606. preparation
  118607. triesters
  118608. palladium
  118609. catalyzed
  118610. vicinal
  118611. preparation
  118612. trifluoromethyl
  118613. ketones
  118614. related
  118615. fluorinat
  118616. preparation
  118617. properties
  118618. reactions
  118619. carbonyl
  118620. oxides
  118621. preparation
  118622. reactions
  118623. physical
  118624. properties
  118625. organobismu
  118626. preparations
  118627. preparative
  118628. preparative
  118629. acetylenic
  118630. chemistry
  118631. preparative
  118632. biotransformations
  118633. whole
  118634. cells
  118635. isolated
  118636. preparative
  118637. flash
  118638. vacuum
  118639. pyrolysis
  118640. review
  118641. flash
  118642. vacuum
  118643. preparative
  118644. flash
  118645. vacuum
  118646. thermolysis
  118647. short
  118648. synthesis
  118649. preparative
  118650. polar
  118651. organometallic
  118652. chemistry
  118653. prepare
  118654. prepared
  118655. preparing
  118656. prepartion
  118657. prepn
  118658. prepn
  118659. diels
  118660. alder
  118661. reactions
  118662. hetero
  118663. substituted
  118664. prepuration
  118665. prescriptions
  118666. prescriptions
  118667. ingredients
  118668. controlled
  118669. formati
  118670. prescursors
  118671. presence
  118672. present
  118673. presentation
  118674. presentation
  118675. preservation
  118676. pressK
  118677. press
  118678. press
  118679. press
  118680. press/oxford
  118681. pressman
  118682. pressure
  118683. preston
  118684. preston
  118685. stevens
  118686. tennant
  118687. benzimidazoles
  118688. conge
  118689. prestwich
  118690. preswinolide
  118691. pretsch
  118692. preussin
  118693. preventing
  118694. price
  118695. price
  118696. william
  118697. silva
  118698. artur
  118699. cavaleiro
  118700. styrylc
  118701. priciple
  118702. priess
  118703. prilezhaeva
  118704. primary
  118705. primary
  118706. nitro
  118707. compounds
  118708. source
  118709. heterocyclic
  118710. primary
  118711. photoprocesses
  118712. transition
  118713. metal
  118714. complexes
  118715. prime
  118716. primer
  118717. primer
  118718. primers
  118719. primory
  118720. principal
  118721. principle
  118722. principles
  118723. principles
  118724. applications
  118725. organotransition
  118726. metal
  118727. chemis
  118728. principles
  118729. synthetic
  118730. applications
  118731. crown
  118732. ether
  118733. chemist
  118734. principles
  118735. electrochemistry
  118736. principles
  118737. molecular
  118738. recognition
  118739. prins
  118740. print
  118741. prinzbach
  118742. prismanes
  118743. proaporphine
  118744. probe
  118745. probed
  118746. probes
  118747. probes
  118748. probing
  118749. probing
  118750. nature
  118751. polycyclic
  118752. conjugated
  118753. dianions
  118754. probing
  118755. specificity
  118756. synthetically
  118757. useful
  118758. enzymes
  118759. problem
  118760. problem
  118761. solving
  118762. organic
  118763. synthesis
  118764. false
  118765. steps
  118766. failed
  118767. problems
  118768. proced
  118769. procedure
  118770. dures
  118771. procedures
  118772. procedures
  118773. nickel
  118774. catalyzed
  118775. conversion
  118776. olefinic
  118777. proceed
  118778. proceedin
  118779. proceeding
  118780. proceedings
  118781. proceeds
  118782. process
  118783. roved
  118784. preparation
  118785. versatile
  118786. ketoester
  118787. processability
  118788. processes
  118789. processes
  118790. prochiral
  118791. prochirality
  118792. procter
  118793. proctor
  118794. prodger
  118795. prodrugs
  118796. produce
  118797. produced
  118798. producing
  118799. productV
  118800. product
  118801. ability
  118802. kinetically-controll
  118803. organic
  118804. reactions
  118805. productionS
  118806. productive
  118807. products\
  118808. products
  118809. fessional
  118810. professional/chapman
  118811. professor
  118812. profiles
  118813. profiles
  118814. proflles
  118815. progeny
  118816. progess
  118817. programn
  118818. programme
  118819. programmed
  118820. programs
  118821. progress
  118822. progress
  118823. progress
  118824. hydroazulene
  118825. synthesis
  118826. progress
  118827. oligosaccharide
  118828. synthesis
  118829. through
  118830. orthogon
  118831. progress
  118832. chemistry
  118833. isobenzofurans
  118834. applications
  118835. progress
  118836. chemistry
  118837. perhalomethanesulphe
  118838. halides
  118839. progress
  118840. chemistry
  118841. sulfilimines
  118842. progress
  118843. chemistry
  118844. derivatives
  118845. trivalent
  118846. progress
  118847. field
  118848. physiologically
  118849. active
  118850. lanosterol
  118851. progress
  118852. fischer
  118853. indole
  118854. reaction
  118855. progress
  118856. fischer
  118857. indole
  118858. reaction
  118859. review
  118860. progress
  118861. heteryne
  118862. field
  118863. progress
  118864. towards
  118865. total
  118866. synthesis
  118867. ene-diyne
  118868. antica
  118869. prohlem
  118870. proidakov
  118871. projection
  118872. prokof'ef
  118873. prokof'ev
  118874. prokopov
  118875. proliferation
  118876. proline
  118877. proline-catalysed
  118878. prolinol-derived
  118879. prolucts
  118880. promising
  118881. promotedu
  118882. omoting
  118883. pronucleophiles
  118884. proof
  118885. propadienes
  118886. propadienylC
  118887. propadienylidene
  118888. propadienylidene
  118889. propane
  118890. propane-13-diols
  118891. propanediol
  118892. propanol
  118893. propanone
  118894. propargylC
  118895. allenyl
  118896. organometallics
  118897. propargyl/allenyl
  118898. propargylamines
  118899. propargylene
  118900. propargyli
  118901. propargylic
  118902. propargyllithium
  118903. propargyloxycoumarin
  118904. propargylsilanes
  118905. prope
  118906. propellanes
  118907. propen
  118908. propene
  118909. propeniminium
  118910. propenoate
  118911. propenolates
  118912. propenyl
  118913. proper
  118914. properities
  118915. properties
  118916. properties
  118917. rties
  118918. reactions
  118919. ylidenemalononitrile
  118920. properties
  118921. electron
  118922. defficient
  118923. 13-diene
  118924. complexes
  118925. properties
  118926. se-se
  118927. te-te
  118928. bonds
  118929. activation
  118930. homonu
  118931. property
  118932. propionates
  118933. propionic
  118934. propionitriles
  118935. propiophenone
  118936. proposal
  118937. proposals
  118938. proprochiral
  118939. propylaminoethyl
  118940. propylammonium
  118941. propylene
  118942. propyne
  118943. propynyl
  118944. propynylidenes
  118945. proskurnina
  118946. prosopinine
  118947. prospect
  118948. prospects
  118949. prospects
  118950. stereocontrol
  118951. reduction
  118952. aromatic
  118953. pross
  118954. radom
  118955. theoretical
  118956. approach
  118957. substituent
  118958. intera
  118959. prostacyclin
  118960. prostacyclins
  118961. prostaglandin
  118962. prostaglandin
  118963. synthesis
  118964. three
  118965. component
  118966. coupling
  118967. prostaglandinsf
  118968. prostaglandins
  118969. thromboxanes
  118970. leukotrienes
  118971. related
  118972. arachid
  118973. prostakov
  118974. prostakov
  118975. gaivoronskaya
  118976. gamma
  118977. piperidinones
  118978. organ
  118979. prostereoisomerism
  118980. protasiewicz
  118981. protease
  118982. protease-catalyzed
  118983. protease-catalyzed
  118984. kinetically
  118985. controlled
  118986. peptide
  118987. synthesis
  118988. proteases
  118989. proteau
  118990. protec
  118991. protected
  118992. protecting
  118993. protecting
  118994. groups
  118995. protecting
  118996. groups
  118997. carboxylic
  118998. acids
  118999. protecting
  119000. groups
  119001. sulfur
  119002. compounds
  119003. protection
  119004. protections
  119005. protective
  119006. protective
  119007. group
  119008. strategies
  119009. synthesis
  119010. functionaliz
  119011. protective
  119012. groups
  119013. organic
  119014. synthesis
  119015. protein
  119016. protein
  119017. overproduction
  119018. organic
  119019. chemists
  119020. proteins
  119021. proteins
  119022. d-chiral
  119023. world
  119024. proteoglycans
  119025. proteolytic
  119026. protic
  119027. protn
  119028. protoberberine
  119029. protoberberines
  119030. protocol
  119031. ocols
  119032. proton
  119033. proton
  119034. exchange
  119035. amides
  119036. surprises
  119037. simple
  119038. systems
  119039. proton
  119040. transfer
  119041. intramolecularly
  119042. hydrogen-bonded
  119043. acids
  119044. protective
  119045. group
  119046. strategies
  119047. synthesis
  119048. functionaliz@
  119049. protocols@
  119050. pseudo-sugar
  119051. publishing
  119052. pyramidalised
  119053. pyrazoles
  119054. fused
  119055. six-membered
  119056. heterocyclic
  119057. rings
  119058. pyridines
  119059. their
  119060. benzo
  119061. derivatives
  119062. structure@
  119063. pyridones
  119064. pyrrazoline@
  119065. pyrrolidines
  119066. quaternary
  119067. quinodimethane
  119068. quinonoid
  119069. johnstone
  119070. wilby
  119071. entwhistle
  119072. little
  119073. intramolecular
  119074. trap@
  119075. transition
  119076. metal
  119077. catalyzed
  119078. reactions
  119079. organic
  119080. friedlina
  119081. velichko
  119082. synthetic
  119083. applications
  119084. grimes
  119085. reactions
  119086. metallocarboranes
  119087. organometallic
  119088. tachikawa
  119089. terada
  119090. tomita
  119091. iwaoka
  119092. synthesis
  119093. rac-78-epoxy-4-basme@
  119094. radical
  119095. radical
  119096. chemistry
  119097. associated
  119098. thiocarbonyl
  119099. group
  119100. proton-ionizable
  119101. proton-ionizable
  119102. crown
  119103. ethers
  119104. short
  119105. review
  119106. proton-transfer
  119107. proton-transfer
  119108. reactions
  119109. between
  119110. oxygen
  119111. protonated
  119112. protonation
  119113. protonic
  119114. protons
  119115. protopine
  119116. protopopova
  119117. protoporphyrin
  119118. protosolvated
  119119. protostereoisomerism
  119120. protostereoisomerism
  119121. prochirality
  119122. prototropic
  119123. prototropic
  119124. routes
  119125. 15-dipoles
  119126. 12-ylides
  119127. applic
  119128. prototype
  119129. protsenko
  119130. provide
  119131. providing
  119132. provoking
  119133. prowse
  119134. proximal
  119135. proximity
  119136. pruett
  119137. hydroformylation
  119138. 1978171
  119139. advances
  119140. organometall
  119141. przemyslaw
  119142. przheval'skii
  119143. pschorr
  119144. pseudo
  119145. pseudo
  119146. amino
  119147. acids
  119148. their
  119149. incorporation
  119150. peptide
  119151. synthe
  119152. pseudo-oligosacchari
  119153. pseudo-sugar
  119154. pseudo-sugar
  119155. pseudo-sugars
  119156. pseudoazulenes
  119157. pseudobase
  119158. pseudobases
  119159. pseudochalcogens
  119160. pseudoephedine
  119161. pseudoephedrine
  119162. pseudohalides
  119163. pseudohalogens
  119164. pseudoindoxyl
  119165. pseudomonas
  119166. pseudomonas
  119167. fluorescens
  119168. lipase
  119169. asymmetric
  119170. synthesis
  119171. pseudomonic
  119172. pseudooxocarbons
  119173. pseudopterane
  119174. pseudopteranoids
  119175. pseudopterolide
  119176. pseudorotation
  119177. psychobiological
  119178. ptaquilosin
  119179. pteridines
  119180. pteridines
  119181. properties
  119182. reactivities
  119183. biological
  119184. significan
  119185. publication
  119186. publications
  119187. published
  119188. publishers
  119189. publishing
  119190. publishing
  119191. puddephatt
  119192. pudova
  119193. pudovik
  119194. pudovik
  119195. konovalova
  119196. addition
  119197. reactions
  119198. esters
  119199. pulse
  119200. pumilio
  119201. pumiliotoxin
  119202. pummerer
  119203. pummerer
  119204. cyclization
  119205. arnstein
  119206. tripeptide
  119207. analogues
  119208. pummerer-diels-alder
  119209. pummerer-type
  119210. pungent
  119211. purdie
  119212. purdie
  119213. brittain
  119214. harry
  119215. analytical
  119216. applications
  119217. purdum
  119218. purdy
  119219. reviews
  119220. organometallic
  119221. chemistry
  119222. purely
  119223. purification
  119224. purine
  119225. purines
  119226. purities
  119227. purity
  119228. purrington
  119229. pursuit
  119230. pursuits
  119231. purvaneckas
  119232. pusch
  119233. push-pull-substitute
  119234. pushkara
  119235. putala
  119236. putala
  119237. lemenovskii
  119238. reactions
  119239. diazoalkanes
  119240. putative
  119241. putrescine
  119242. puyoug
  119243. pykef
  119244. stephen
  119245. diastereoselective
  119246. reactions
  119247. sulfoximines
  119248. pyramidal
  119249. pyramidal
  119250. carbocations
  119251. pyramidalised
  119252. pyramidalised
  119253. pyramidalised
  119254. alkenes
  119255. pyramidalization
  119256. pyramidalized
  119257. pyran
  119258. pyran-2-ones
  119259. pyranes
  119260. pyrano
  119261. pyranocoumarins
  119262. pyranopyrazoles
  119263. pyranoquinones
  119264. ose-derived
  119265. pyranose-derived
  119266. dienes
  119267. conjugated
  119268. enals
  119269. preparation
  119270. pyranoses
  119271. pyranosides
  119272. pyranotropanes
  119273. pyrans
  119274. pyrans
  119275. fused
  119276. pyrans
  119277. structure
  119278. pyrans
  119279. fused
  119280. pyrans
  119281. reactivity
  119282. pyrans
  119283. fused
  119284. pyrans
  119285. synthesis
  119286. applications
  119287. pyrazine
  119288. pyrazines
  119289. pyrazines
  119290. their
  119291. benzo
  119292. derivatives
  119293. pyrazol
  119294. pyrazol-1-yl
  119295. pyrazolacrylonitrile
  119296. pyrazolato
  119297. pyrazole
  119298. pyrazole
  119299. 1-oxides
  119300. 12-dioxides
  119301. derivatives
  119302. pyrazoles
  119303. pyrazoles
  119304. their
  119305. benzo
  119306. derivatives
  119307. pyrazoles
  119308. fused
  119309. six-membered
  119310. heterocyclic
  119311. rings
  119312. pyrazoles
  119313. fused
  119314. six-membered
  119315. heterocyclic
  119316. rings
  119317. pyrazolidinediones
  119318. pyrazolidinones
  119319. pyrazoline
  119320. pyrazolines
  119321. pyrazolo
  119322. pyrazolone
  119323. pyrazolones
  119324. pyrazolopyridines
  119325. pyrazolothiazoles
  119326. pyrazolyl
  119327. pyrene
  119328. pyrenylaminyl
  119329. pyrethrium
  119330. pyrethroid
  119331. pyrethroids
  119332. pyridazine
  119333. pyridazines
  119334. pyridazines
  119335. their
  119336. benzo
  119337. derivatives
  119338. pyridazino
  119339. pyridazinone
  119340. pyridazinones
  119341. pyridin
  119342. pyridine
  119343. pyridine
  119344. nucleophilic
  119345. recyclisations
  119346. pyridines
  119347. pyridines
  119348. their
  119349. benzo
  119350. derivatives
  119351. structure
  119352. pyridines
  119353. their
  119354. benzo
  119355. derivatives
  119356. reactivity
  119357. pyridines
  119358. their
  119359. benzo
  119360. derivatives
  119361. reactivity
  119362. pyridines
  119363. their
  119364. benzo
  119365. derivatives
  119366. reactivity
  119367. non-a
  119368. pyridines
  119369. their
  119370. benzo
  119371. derivatives
  119372. synthesis
  119373. pyridines
  119374. their
  119375. benzo
  119376. derivatives
  119377. applications
  119378. pyridinethiones
  119379. pyridinium
  119380. pyridinium
  119381. chlorochromate
  119382. versatile
  119383. oxidant
  119384. organic
  119385. pyridiniumiodides
  119386. pyridinocrowns
  119387. pyridinones
  119388. pyridinophanes
  119389. pyridinyl
  119390. pyrido
  119391. pyridoacridine
  119392. pyridoacridines
  119393. pyridocarbazole
  119394. pyridocryptands
  119395. pyridodiazines
  119396. pyridodiazines
  119397. their
  119398. benzo
  119399. derivatives
  119400. pyridodiindoles
  119401. pyridone
  119402. pyridones
  119403. pyridones
  119404. pyridoquinolines
  119405. pyridyl
  119406. pyridylphosphines
  119407. pyridylsilanes
  119408. pyridylthioesters
  119409. pyriformis
  119410. pyrilium
  119411. pyrimidin
  119412. pyrimidine
  119413. pyrimidine
  119414. n-oxides
  119415. synthesis
  119416. structures
  119417. chemical
  119418. proper
  119419. pyrimidines
  119420. pyrimidines
  119421. their
  119422. benzo
  119423. derivatives
  119424. pyrimidinethiones
  119425. pyrimidinones
  119426. pyrimidoazepines
  119427. pyrimidoblamic
  119428. pyrimidones
  119429. pyrimidyl
  119430. pyroglutamates
  119431. pyrolizidine
  119432. pyrolysis
  119433. pyrolysis
  119434. azides
  119435. mechanistic
  119436. implications
  119437. pyrolytic
  119438. pyrolytic
  119439. methods
  119440. organic
  119441. chemistry
  119442. pyrone
  119443. pyrones
  119444. pyrrazoline
  119445. pyrrol
  119446. pyrrole
  119447. pyrrole
  119448. pyrrolidine
  119449. piperidine
  119450. azepine
  119451. alkaloids
  119452. pyrrolenines
  119453. pyrroles
  119454. pyrroles
  119455. their
  119456. benzo
  119457. derivatives
  119458. ructure
  119459. pyrroles
  119460. their
  119461. benzo
  119462. derivatives
  119463. reactivity
  119464. pyrroles
  119465. their
  119466. benzo
  119467. derivatives
  119468. synthesis
  119469. appli
  119470. pyrroles
  119471. synthesis
  119472. reactivity
  119473. physical
  119474. proper
  119475. pyrroles
  119476. synthesis
  119477. physical
  119478. chemical
  119479. pyrroles
  119480. fused
  119481. six-membered
  119482. heterocyclic
  119483. rings
  119484. a-fuse
  119485. pyrroles
  119486. fused
  119487. six-membered
  119488. heterocyclic
  119489. rings
  119490. pyrrolidine
  119491. pyrrolidines
  119492. pyrrolidines
  119493. pyrrolidinocycloalke
  119494. pyrrolidinones
  119495. pyrroline
  119496. pyrrolines
  119497. pyrrolinones
  119498. pyrrolizidine
  119499. lizidine
  119500. alkaloid
  119501. synthesis
  119502. supinidine
  119503. pyrrolizidine
  119504. alkaloids
  119505. pyrrolizidines
  119506. pyrrolizin
  119507. pyrrolizin
  119508. pyrrolizine
  119509. pyrrolizine
  119510. chemistry
  119511. pyrrolizines
  119512. pyrrolo
  119513. pyrrolo
  119514. indoles
  119515. intramolecular
  119516. reaction
  119517. pyrrolodiazines
  119518. pyrroloindoles
  119519. pyrrolophenanthridon
  119520. pyrrolopyrimidines
  119521. pyrroloquinolines
  119522. pyrrolyl
  119523. pyrylinn
  119524. pyrylium
  119525. pyrylium
  119526. salts
  119527. pytlewski
  119528. broxterman
  119529. hogeveen
  119530. kingma
  119531. qiang
  119532. qinghaosu
  119533. qiurong
  119534. qlefins
  119535. quack
  119536. quadratic
  119537. quadricyclane
  119538. quadrone
  119539. qualitative
  119540. quality
  119541. quantification
  119542. quantification
  119543. steric
  119544. effects
  119545. organometallic
  119546. chemistry
  119547. quantifying
  119548. quantitation
  119549. quantitative
  119550. quantitative
  119551. modeling
  119552. proximity
  119553. effects
  119554. organic
  119555. reacti
  119556. quantitative
  119557. structure
  119558. activity
  119559. relationships
  119560. benzodi
  119561. quantities
  119562. quantitites
  119563. quantum
  119564. quantum-chemical
  119565. quaranta
  119566. quarter
  119567. quassinoid
  119568. quassinoids
  119569. quast
  119570. quaterary
  119571. quaternary
  119572. quaternary
  119573. quaternary
  119574. ammonium
  119575. compounds
  119576. organic
  119577. synthesis
  119578. quaternization
  119579. queener
  119580. queguiner
  119581. queguiner
  119582. marsais
  119583. francis
  119584. snieckus
  119585. victor
  119586. epsztajn
  119587. quenchers
  119588. quenching
  119589. queneauu
  119590. quentin
  119591. quessy
  119592. quest
  119593. question
  119594. quici
  119595. quiclet
  119596. quiescent
  119597. heterocyclic
  119598. chemistry
  119599. phosphorus
  119600. systems
  119601. quina
  119602. quinazolin
  119603. quinazoline
  119604. quinazolines
  119605. quinazolinocarboline
  119606. quinazolinones
  119607. quinazolone
  119608. quinic
  119609. quiniou
  119610. quiniou
  119611. thioamide
  119612. vinylogs
  119613. 198110
  119614. phosphorus
  119615. sulfur
  119616. quinkert
  119617. quino
  119618. quinocarcin
  119619. quinocyclopropenes
  119620. quinodimethane
  119621. quinodimethane
  119622. quinodimethanes
  119623. quinoid
  119624. quinoline
  119625. quinoline
  119626. 1-oxides
  119627. quinoline
  119628. analogues
  119629. ortho-quinodimethane
  119630. quinoline
  119631. quinazoline
  119632. acridone
  119633. alkaloids
  119634. quinoline-58-quinone
  119635. quinolinequinone
  119636. quinolines
  119637. quinolinetriones
  119638. quinolinium
  119639. quinolizidine
  119640. quinolizidine-type
  119641. quinolizidines
  119642. quinolizine
  119643. quinolizines
  119644. quinolizinium
  119645. quinolizinium
  119646. salts
  119647. quinolones
  119648. quinols
  119649. quinone
  119650. quinones
  119651. quinonoid
  119652. quinou
  119653. quinoxaline
  119654. quintana
  119655. quinteiro
  119656. quintero
  119657. quintessential
  119658. quinuclidine
  119659. quite
  119660. quivalent
  119661. qunia
  119662. qureshi
  119663. abramovitch
  119664. shinkai
  119665. accounts
  119666. cherkasov
  119667. kutyrev
  119668. pudovik
  119669. tetrahedron
  119670. firestone
  119671. diradical
  119672. mechanism
  119673. dipolar
  119674. cycloadditi
  119675. jones
  119676. chemistry
  119677. pyrroles
  119678. academic
  119679. khmel'nitskii
  119680. efremov
  119681. rearrangements
  119682. sulfoxi
  119683. komoroski
  119684. studies
  119685. biopo
  119686. johnstone
  119687. wilby
  119688. entwhistle
  119689. 23-o-isopropylideneg
  119690. stereoselective
  119691. organic
  119692. anderson
  119693. synthesis
  119694. synthetic
  119695. applications
  119696. appel
  119697. angew
  119698. tertiary
  119699. phosphine/tet
  119700. cundall
  119701. pereira
  119702. exeitation
  119703. deexcitation
  119704. gammill
  119705. wilson
  119706. bryson
  119707. synth
  119708. merrifield
  119709. angew
  119710. solid
  119711. bolton
  119712. williams
  119713. homolytic
  119714. bonnett
  119715. nicolaidou
  119716. nitrite
  119717. environment
  119718. bowen
  119719. london
  119720. redox
  119721. enzymes
  119722. kerber
  119723. organometallic
  119724. organoiron
  119725. carlson
  119726. lundstedt
  119727. albano
  119728. scand
  119729. cognition
  119730. catalysis
  119731. using
  119732. molecular
  119733. clefts
  119734. hamilton
  119735. campaigne
  119736. dithiole
  119737. dithiolium
  119738. systems
  119739. howells
  119740. mccown
  119741. trifluoromethanesulf
  119742. little
  119743. intramolecular
  119744. rieke
  119745. fortschritte
  119746. forschung
  119747. topsom
  119748. nature
  119749. analysis
  119750. substituent
  119751. electronic
  119752. deslauriers
  119753. smith
  119754. conformation
  119755. structure
  119756. deslongchamps
  119757. synthetic
  119758. studies
  119759. towards
  119760. ryanodine
  119761. 491329
  119762. dolbier
  119763. kinetic
  119764. duction
  119765. diimide
  119766. banks
  119767. tatlow
  119768. fluor
  119769. guide
  119770. gawley
  119771. oxygen
  119772. nitrogen
  119773. assis
  119774. gawley
  119775. synthesis
  119776. robinson
  119777. annelation
  119778. marchand
  119779. operational
  119780. criteria
  119781. evaluatio
  119782. moore
  119783. algal
  119784. lsoprenoids
  119785. marine
  119786. natural
  119787. products
  119788. moore
  119789. volatile
  119790. compounds
  119791. marine
  119792. algae
  119793. engel
  119794. phosphonates
  119795. analogues
  119796. natural
  119797. phosphates
  119798. esmail
  119799. kurzer
  119800. synthesis
  119801. chemistry
  119802. transition
  119803. metal
  119804. catalyzed
  119805. reactions
  119806. organic
  119807. filler
  119808. developments
  119809. chemistry
  119810. filler
  119811. pentafluorophenyl
  119812. group
  119813. effects
  119814. reactivity
  119815. crabtree
  119816. organometallic
  119817. chemist
  119818. huisgen
  119819. tetramethylene
  119820. intermediates
  119821. intercepted
  119822. huisgen
  119823. electrocyclic
  119824. opening
  119825. reactions
  119826. ethylene
  119827. huisgen
  119828. schug
  119829. steiner
  119830. huisgen
  119831. tetracyanoethylene
  119832. ethers
  119833. model
  119834. bergeron
  119835. methods
  119836. select
  119837. clemens
  119838. diketene
  119839. review
  119840. haines
  119841. leigh
  119842. olefin
  119843. hayward
  119844. novel
  119845. heterocycles
  119846. relate
  119847. taylor
  119848. synthesis
  119849. organocopper
  119850. conjugate
  119851. addit
  119852. stoodley
  119853. aspects
  119854. heterocyclic
  119855. synthesis
  119856. dieter
  119857. tetrahedron
  119858. alpha
  119859. ketene
  119860. dithioa
  119861. friedlina
  119862. velichko
  119863. synthetic
  119864. applications
  119865. keese
  119866. angew
  119867. methods
  119868. prepar
  119869. freidlina
  119870. terent'ev
  119871. radical
  119872. rearrangements
  119873. chemicals
  119874. which
  119875. control
  119876. plant
  119877. growth
  119878. coates
  119879. biogenetic
  119880. rearrangements
  119881. terpenes
  119882. moriarty
  119883. prakash
  119884. hypervale
  119885. ottenbrite
  119886. initio
  119887. wenger
  119888. angew
  119889. synthesis
  119890. mayer
  119891. elemental
  119892. sulfur
  119893. reactions
  119894. organic
  119895. chemistry
  119896. miethchen
  119897. kroger
  119898. reaction
  119899. muller
  119900. chemistry
  119901. organometallic
  119902. muller
  119903. chemistry
  119904. organochlorosil
  119905. butler
  119906. tetraacetate
  119907. acetoxyla
  119908. butler
  119909. diazotization
  119910. heteroc
  119911. butler
  119912. recent
  119913. advances
  119914. tetrazole
  119915. chemistry
  119916. grimes
  119917. reactions
  119918. metallocarboranes
  119919. organometallic
  119920. noack
  119921. schwetlich
  119922. cycloadditions
  119923. evstigneeva
  119924. myagkova
  119925. pardo
  119926. santelli
  119927. synthesis
  119928. schmidt
  119929. hetero
  119930. diels
  119931. alder
  119932. schmidt
  119933. angew
  119934. heterocyclic
  119935. syste
  119936. schmidt
  119937. angew
  119938. methods
  119939. rossi
  119940. synthesis
  119941. achiral
  119942. components
  119943. insect
  119944. pheromones
  119945. davidson
  119946. eleventh
  119947. internatio
  119948. varma
  119949. kabalka
  119950. heterocycles
  119951. nitroalk
  119952. scheffold
  119953. chimia
  119954. vitamin
  119955. catalyst
  119956. thermochemistry
  119957. groups
  119958. chemistry
  119959. double
  119960. sheldon
  119961. catalytic
  119962. oxidation
  119963. sustmann
  119964. charge
  119965. lalonde
  119966. sulfur
  119967. containing
  119968. nuphar
  119969. alkaloids
  119970. tachikawa
  119971. terada
  119972. tomita
  119973. iwaoka
  119974. synthesis
  119975. hoffman
  119976. proced
  119977. oxidation
  119978. stevens
  119979. alkaloid
  119980. synthesis
  119981. total
  119982. synthesis
  119983. natura
  119984. stevens
  119985. general
  119986. methods
  119987. alkaloid
  119988. synthesis
  119989. valters
  119990. chain
  119991. isomeric
  119992. anionic
  119993. rearrangements
  119994. organosilicon
  119995. german
  119996. r-te-cn
  119997. r-te-hal4
  119998. r-te-m
  119999. r-te-ocn
  120000. r-te-oh
  120001. r-te-r
  120002. r-teh
  120003. r-tehal2
  120004. r2c-x-cr2
  120005. raadt
  120006. raban
  120007. rabenau
  120008. raber
  120009. rabideau
  120010. rabideau
  120011. conformational
  120012. analysis
  120013. cyclohexadien
  120014. rabideau
  120015. peter
  120016. marcinow
  120017. zbigniew
  120018. birch
  120019. reduction
  120020. rabinovich
  120021. rabinovitz
  120022. rabinovitz
  120023. mordecai
  120024. ayalon
  120025. conjugated
  120026. polycyclic
  120027. rabjohn
  120028. rac-78-epoxy-4-basme
  120029. rac-a58365b
  120030. rac-morphine
  120031. racemates
  120032. racemic
  120033. racemization
  120034. racical
  120035. ractions
  120036. radchenko
  120037. raddatz
  120038. rademacher
  120039. radha
  120040. radhakrishnan
  120041. radhe
  120042. radialenes
  120043. radiation
  120044. radiative
  120045. radica
  120046. radical
  120047. radical
  120048. radical
  120049. saturat
  120050. radical
  120051. addition
  120052. reactions
  120053. radical
  120054. anion
  120055. induced
  120056. reductive
  120057. alkylation
  120058. phenyl
  120059. thioeth
  120060. radical
  120061. anion
  120062. intermediates
  120063. organic
  120064. chemistry
  120065. radical
  120066. elimination
  120067. vicinal
  120068. phenylselenide
  120069. xanthate
  120070. radical
  120071. based
  120072. synthesis
  120073. lactams
  120074. indolones
  120075. dithio
  120076. radical
  120077. brominations
  120078. alkyl
  120079. bromides
  120080. nature
  120081. radical
  120082. brominations
  120083. allkyl
  120084. bromides
  120085. radical
  120086. cascades
  120087. synthesis
  120088. dioxatrinanes
  120089. doubly-annul
  120090. radical
  120091. cations
  120092. reactive
  120093. intermediates
  120094. aromatic
  120095. activa
  120096. radical
  120097. chain
  120098. addition
  120099. benzenethiol
  120100. allenic
  120101. esters
  120102. radical
  120103. chemistry
  120104. associated
  120105. thiocarbonyl
  120106. group
  120107. radical
  120108. chemistry
  120109. associated
  120110. thiocarbonyl
  120111. group
  120112. radical
  120113. cyclization
  120114. allenic
  120115. hydrazones
  120116. asymmetric
  120117. radical
  120118. cyclization
  120119. bromomethyldimethyls
  120120. propargyl
  120121. ethers
  120122. radical
  120123. cyclizations
  120124. sequential
  120125. radical
  120126. reactions
  120127. radical
  120128. cyclizations
  120129. oxime
  120130. ethers
  120131. connected
  120132. aldehyde
  120133. radical
  120134. functionalization
  120135. anomeric
  120136. center
  120137. carbohyd
  120138. radical
  120139. induced
  120140. opening
  120141. bromomethyl
  120142. aziridines
  120143. radical
  120144. where
  120145. organic
  120146. chemistry
  120147. meets
  120148. materials
  120149. science
  120150. radical
  120151. attack
  120152. substitution
  120153. aromatic
  120154. compou
  120155. radical
  120156. kinetics
  120157. mechanistic
  120158. probe
  120159. studies
  120160. radical
  120161. reactions
  120162. retrosynthetic
  120163. planning
  120164. radical
  120165. reactions
  120166. retrosynthetic
  120167. planning
  120168. overall
  120169. radical
  120170. reactions
  120171. natural
  120172. product
  120173. synthesis
  120174. radical
  120175. reactions
  120176. organc
  120177. synthesis
  120178. radical
  120179. translocation
  120180. reactions
  120181. across
  120182. amides
  120183. hydrogen
  120184. radical
  120185. cyclization
  120186. dienes
  120187. stereoselectivit
  120188. radical
  120189. chemistry
  120190. associated
  120191. thiocarbonyl
  120192. group
  120193. radical
  120194. reactions
  120195. steps
  120196. natural
  120197. product
  120198. synthesis@
  120199. radical-based@
  120200. radical-mediated
  120201. brominations
  120202. positions
  120203. carbohydr@
  120204. radicals
  120205. rahman
  120206. basha
  120207. fatima
  120208. studies
  120209. natural
  120210. product@
  120211. rajopadhye@
  120212. ramos
  120213. tombo
  120214. gerardo
  120215. bellus
  120216. daniel
  120217. chirality
  120218. prote@
  120219. filler
  120220. oxazolones
  120221. oxazoles
  120222. chemistry
  120223. earth
  120224. triflates
  120225. organic
  120226. synthesis@
  120227. rational
  120228. design
  120229. orthogonal
  120230. receptor-ligand
  120231. combinations@
  120232. rationally@
  120233. re-evaluation@
  120234. reaction
  120235. reaction
  120236. branching
  120237. extreme
  120238. kinetic
  120239. isotope
  120240. effects
  120241. electrophiles@
  120242. reactions
  120243. organoboron
  120244. compounds@
  120245. reactions
  120246. substituted
  120247. 2-butene-14-diyl
  120248. magnesium
  120249. complexe@
  120250. reactive
  120251. reactivity
  120252. reactivity
  120253. selectivity
  120254. lewis
  120255. acid-catalyzed
  120256. diels-ald@
  120257. radical-based
  120258. radical-chain
  120259. radical-chain
  120260. electron-transfer
  120261. dehalogenation
  120262. reactions
  120263. radical-mediated
  120264. al-mediated
  120265. brominations
  120266. positions
  120267. carbohydr
  120268. radicals
  120269. radicals
  120270. radicophiles
  120271. radioactive
  120272. radioiodination
  120273. radiolabeled
  120274. radiolysis
  120275. radionuclide
  120276. radiopharmaceuticals
  120277. stanislav
  120278. bouzard
  120279. daniel
  120280. recent
  120281. advances
  120282. synthes
  120283. radner
  120284. radom
  120285. raduz
  120286. raevskii
  120287. rafael
  120288. raffaelli
  120289. rafikov
  120290. ragault
  120291. ragnarsson
  120292. ragnarsson
  120293. grehn
  120294. novel
  120295. gabriel
  120296. reagents
  120297. accts
  120298. rague
  120299. rahimah
  120300. rahmanV
  120301. rahman
  120302. natural
  120303. products
  120304. monoterpene
  120305. rahman
  120306. ahmad
  120307. viqar
  120308. uddin
  120309. natural
  120310. rahman
  120311. basha
  120312. fatima
  120313. studies
  120314. natural
  120315. product
  120316. rahman
  120317. studies
  120318. natural
  120319. products
  120320. chemistry
  120321. rahman
  120322. handbook
  120323. natural
  120324. products
  120325. diter
  120326. rahman
  120327. zahir
  120328. stereoselective
  120329. synthesis
  120330. organ
  120331. rahman
  120332. studies
  120333. natural
  120334. products
  120335. chemistry
  120336. raifel'd
  120337. raifel'd
  120338. vaisman
  120339. asymmetric
  120340. epoxidation
  120341. russian
  120342. raimondi
  120343. rainer
  120344. rainina
  120345. rajanbabu
  120346. rajanbabu
  120347. casalnuovo
  120348. electronic
  120349. effects
  120350. asymmetri
  120351. rajanbabu
  120352. stereochemistry
  120353. intramolecular
  120354. radical
  120355. rajappa
  120356. rajappa
  120357. synthesis
  120358. heteroaromatic
  120359. nitro
  120360. rajappa
  120361. nitroenamines
  120362. preparation
  120363. structure
  120364. synthetic
  120365. rajca
  120366. rajca
  120367. andrzej
  120368. polyarylmethyl
  120369. polyradicals
  120370. advances
  120371. rajca
  120372. andrzej
  120373. organic
  120374. diradicals
  120375. polyradicals
  120376. rajender
  120377. rajeswari
  120378. rajopadhye
  120379. rajzmann
  120380. rakhimov
  120381. rakhmankulov
  120382. rakhmankulov
  120383. kantor
  120384. karakhanov
  120385. catalyzed
  120386. rakhmatulina
  120387. rakitin
  120388. rakowski
  120389. ralicals
  120390. ralph
  120391. ramachandran
  120392. ramada
  120393. ramadan
  120394. ramadas
  120395. ramage
  120396. ramage
  120397. organophosphorus
  120398. reagents
  120399. synthesis
  120400. pepti
  120401. ramaiah
  120402. ramamurthy
  120403. ramamurthy
  120404. weiss
  120405. richard
  120406. hammond
  120407. george
  120408. model
  120409. raman
  120410. ramana
  120411. ramberg
  120412. ramberg
  120413. backlund
  120414. reactions
  120415. phosphonium
  120416. salts
  120417. ramberg-backlund
  120418. ramesh
  120419. ramification
  120420. ramifications
  120421. ramirez
  120422. ramirez
  120423. maracek
  120424. phosphorylation
  120425. means
  120426. cyclic
  120427. ramon
  120428. ramos
  120429. ramos
  120430. tombo
  120431. gerardo
  120432. bellus
  120433. daniel
  120434. chirality
  120435. prote
  120436. ramphal
  120437. ramsden
  120438. ramsden
  120439. heterocyclic
  120440. betain
  120441. derivatives
  120442. alternant
  120443. ramsden
  120444. semiempirical
  120445. organic
  120446. chemists
  120447. 197814
  120448. ramsden
  120449. christopher
  120450. bonding
  120451. molecular
  120452. orbitals
  120453. rancourt
  120454. randaccio
  120455. randall
  120456. randic
  120457. randic
  120458. milan
  120459. orthogonal
  120460. molecular
  120461. descriptors
  120462. journal
  120463. randolph
  120464. random
  120465. randy
  120466. raner
  120467. raney
  120468. ranganathan
  120469. rangansthan
  120470. range
  120471. brindaban
  120472. borohydride
  120473. reducing
  120474. agent
  120475. trends
  120476. biocatalysis
  120477. presence
  120478. pushkara
  120479. photoreactivity
  120480. thiocarbonyl
  120481. compounds
  120482. filler
  120483. oxazolones
  120484. oxazoles
  120485. chemistry
  120486. filler
  120487. oxazolones
  120488. oxazoles
  120489. chemistry
  120490. rapamycin
  120491. raphael
  120492. rapid
  120493. rapoport
  120494. rappa
  120495. rappoport
  120496. rappoport
  120497. nucleophilic
  120498. vinylic
  120499. substitution
  120500. single
  120501. multi
  120502. rappoport
  120503. rapid
  120504. steps
  120505. nucleophilic
  120506. vinylic
  120507. additi
  120508. rarez
  120509. rare-earth-metal
  120510. rare-earth-metal
  120511. trifluoromethanesulf
  120512. water-tolerant
  120513. rasch
  120514. rashed
  120515. rasmussen
  120516. rasmusson
  120517. rassat
  120518. rasteikiene
  120519. rastogi
  120520. rastoll
  120521. ratcliffe
  120522. rate-determining
  120523. rategy
  120524. rates
  120525. rathi
  120526. rathke
  120527. rational
  120528. rationalize
  120529. rationally
  120530. ratios
  120531. ratnam
  120532. ratonJ
  120533. ratovskii
  120534. rattay
  120535. raubenheimer
  120536. rauch
  120537. rauchschwalbe
  120538. orbital
  120539. interaction
  120540. theory
  120541. organic
  120542. chemistry
  120543. raulins
  120544. raumacline
  120545. rausch
  120546. rauschenbach
  120547. ravelo
  120548. ravid
  120549. ravindar
  120550. ravindranathan
  120551. rawal
  120552. rawdah
  120553. rawson
  120554. raymond
  120555. raynal
  120556. rayner
  120557. rayner
  120558. christopher
  120559. thiols
  120560. sulfides
  120561. sulfoxides
  120562. sulfones
  120563. rayyes
  120564. razdan
  120565. razdan
  120566. total
  120567. synthesis
  120568. cannabinoids
  120569. razuvaev
  120570. razvodovskaya
  120571. razvodovskayn
  120572. rchx2
  120573. re-evaluation
  120574. re-examination
  120575. react
  120576. reactant
  120577. reactants
  120578. reacti
  120579. reactio
  120580. reaction
  120581. reaction
  120582. reaction
  120583. reaction
  120584. reaction
  120585. reaction
  120586. mechanisms
  120587. displayed
  120588. catalytic
  120589. antibodies
  120590. reaction
  120591. halomethyl
  120592. bicyclo
  120593. 1.1.1
  120594. pentane
  120595. strong
  120596. reaction
  120597. dichloro
  120598. chloromethyl
  120599. cyclopropane
  120600. reaction
  120601. ethoxycarbonyl
  120602. pentadienylsilane
  120603. under
  120604. ritter
  120605. reaction
  120606. cyanothioacrylamides
  120607. electron
  120608. reaction
  120609. epoxyalkyl
  120610. silanes
  120611. sulfonyl
  120612. anions
  120613. reaction
  120614. acetylenes
  120615. double-bridged
  120616. triruthenium
  120617. reaction
  120618. b-heteroatom
  120619. substituted
  120620. b-unsaturated
  120621. acylsil
  120622. reaction
  120623. benzocyclobutenoxide
  120624. aldehydes
  120625. synthesis
  120626. reaction
  120627. carbenes
  120628. divalent
  120629. sulfur
  120630. compounds
  120631. reaction
  120632. enaminonitriles
  120633. isocyanates
  120634. synthesis
  120635. reaction
  120636. ethyl
  120637. diazonacetate
  120638. thiazole
  120639. thione
  120640. reaction
  120641. halodiaziridines
  120642. electron
  120643. transfer
  120644. reaction
  120645. n-acyl-a-methoxyamin
  120646. organozinc
  120647. reagents
  120648. reaction
  120649. substituted
  120650. oximes
  120651. 2-azomethine
  120652. ylids
  120653. reaction
  120654. phenyl
  120655. diazomethane
  120656. thiazole
  120657. thione
  120658. reaction
  120659. pummerer
  120660. rearrangement
  120661. intermediate
  120662. thiols
  120663. reaction
  120664. pyridinium
  120665. ylides
  120666. reaction
  120667. sodium
  120668. naphthalenide
  120669. methyloxindole
  120670. under
  120671. reaction
  120672. sulfonium
  120673. salts
  120674. formaldehyde
  120675. dithioacetals
  120676. reaction
  120677. substituted
  120678. 133-trichloro-2-aza
  120679. 11-dichlor
  120680. reaction
  120681. trialkylboranes
  120682. nitrones
  120683. novel
  120684. route
  120685. reaction
  120686. unsaturated
  120687. azlactones
  120688. sulfur
  120689. nucleophiles
  120690. reaction
  120691. symmetry
  120692. criteria
  120693. detection
  120694. metastable
  120695. reaction
  120696. systems
  120697. pharmaceutical
  120698. production
  120699. reaction-a
  120700. reaction/electrocycl
  120701. reactiona
  120702. reactionos
  120703. reactionsC
  120704. reactions
  120705. reactions
  120706. reactions
  120707. reactions
  120708. reactions
  120709. reactions
  120710. reactions
  120711. reactions
  120712. reactions
  120713. reactions
  120714. reactions
  120715. 11-dihaloalkenes
  120716. triorganozincates
  120717. novel
  120718. reactions
  120719. thiadiazole
  120720. dicarbonitrile
  120721. reactions
  120722. diaza
  120723. butadienes
  120724. haloketenes
  120725. rearran
  120726. reactions
  120727. 14-dihydropyridines
  120728. reactions
  120729. diaryl-37-dioxabicyc
  120730. 3.3.0
  120731. octane
  120732. lignans
  120733. reactions
  120734. 26-diaryl
  120735. dioxabicyclo
  120736. 3.3.0
  120737. octane
  120738. lignans
  120739. reactions
  120740. thiazolyl
  120741. sydnones
  120742. media
  120743. synthesis
  120744. reactions
  120745. 45-dihydro-5-oxo-13
  120746. oxygen-containing
  120747. reactions
  120748. azaindole
  120749. niobium
  120750. tantalum
  120751. pentachlo
  120752. reactions
  120753. haloallyllithium
  120754. derivatives
  120755. carbon
  120756. reactions
  120757. acetals
  120758. orthoesters
  120759. their
  120760. analogues
  120761. reactions
  120762. activated
  120763. dienes
  120764. aldehydes
  120765. reactions
  120766. anion
  120767. equivalents
  120768. derived
  120769. cyanohydrin
  120770. reactions
  120771. aldehydes
  120772. reactions
  120773. alkynols
  120774. alkynylalkoxycarbene
  120775. metal
  120776. comple
  120777. reactions
  120778. allyl
  120779. propargyl
  120780. allenic
  120781. organometallics
  120782. reactions
  120783. allylsiloanes
  120784. application
  120785. organic
  120786. synthe
  120787. reactions
  120788. alpha
  120789. diazoketones
  120790. ether
  120791. oxygen
  120792. participation
  120793. reactions
  120794. iminophosphoranylide
  120795. carbenoid
  120796. reactions
  120797. annular
  120798. nitrogens
  120799. azines
  120800. electrophiles
  120801. reactions
  120802. aromatic
  120803. diazonium
  120804. salts
  120805. unsaturated
  120806. compo
  120807. reactions
  120808. trichloromethyl
  120809. carbinols
  120810. nucleophile
  120811. reactions
  120812. azines
  120813. imines
  120814. azomethines
  120815. schiff
  120816. bases
  120817. reactions
  120818. azines
  120819. bifunctional
  120820. nucleophiles
  120821. cyclizati
  120822. reactions
  120823. ketoamides
  120824. kinetics
  120825. enolisation
  120826. aceto
  120827. reactions
  120828. b-fluorovinamidinium
  120829. bifunctional
  120830. reactions
  120831. carbon
  120832. disulfide
  120833. review
  120834. reactions
  120835. carbon
  120836. disulfide
  120837. c-nucleophiles
  120838. reactions
  120839. carbonyl
  120840. compounds
  120841. monohalo
  120842. methyleniminiu
  120843. reactions
  120844. chlorocyclophosphaze
  120845. difunctional
  120846. reagents
  120847. reactions
  120848. cycloalkenopyridines
  120849. reactions
  120850. cyclopalladated
  120851. compounds
  120852. alkynes
  120853. pathw
  120854. reactions
  120855. cyclopropene
  120856. derivatives
  120857. electrophiles
  120858. reactions
  120859. diaminosulfoxonium
  120860. ylides
  120861. aldehydes
  120862. prepar
  120863. reactions
  120864. dianions
  120865. carboxylic
  120866. acids
  120867. ester
  120868. enolates
  120869. reactions
  120870. diazoalkanes
  120871. transition
  120872. metal
  120873. complexes
  120874. reactions
  120875. electrophiles
  120876. sigma-bonded
  120877. organotransitio
  120878. reactions
  120879. elemental
  120880. sulfur
  120881. activated
  120882. ammonia
  120883. amines
  120884. reactions
  120885. halodiazirines
  120886. electron
  120887. transfer
  120888. reactions
  120889. heterocyclic
  120890. compounds
  120891. nitrilimines
  120892. reactions
  120893. hydrocarbons
  120894. electrophilic
  120895. transition
  120896. reactions
  120897. valent
  120898. transition
  120899. metal
  120900. compleses
  120901. reactions
  120902. malononitrile
  120903. derivatives
  120904. reactions
  120905. pyrrolidinocycloalke
  120906. phenyl
  120907. benzylid
  120908. reactions
  120909. n-chloramines
  120910. haloamides
  120911. unsaturated
  120912. reactions
  120913. nitrile
  120914. oxides
  120915. nitrilimines
  120916. imidate
  120917. reactions
  120918. nitrones
  120919. ketenes
  120920. reactions
  120921. organic
  120922. peroxo
  120923. compounds
  120924. reactions
  120925. organoboron
  120926. compounds
  120927. reactions
  120928. phosphorus
  120929. chlorides
  120930. carbonyl
  120931. compound
  120932. reactions
  120933. phosphorus-containin
  120934. compounds
  120935. diazo
  120936. compo
  120937. reactions
  120938. polyfluoroketones
  120939. unsaturated
  120940. compounds
  120941. reactions
  120942. pyridines
  120943. pyrimidines
  120944. 135-triazines
  120945. reactions
  120946. radicals
  120947. formation
  120948. c-bond
  120949. reactions
  120950. radicals
  120951. formation
  120952. h-bond
  120953. reactions
  120954. radicals
  120955. formation
  120956. halogen-bond
  120957. reactions
  120958. radicals
  120959. formation
  120960. m-bond
  120961. reactions
  120962. radicals
  120963. formation
  120964. n-bond
  120965. reactions
  120966. radicals
  120967. formation
  120968. o-bond
  120969. reactions
  120970. radicals
  120971. formation
  120972. p-bond
  120973. reactions
  120974. radicals
  120975. formation
  120976. s-bond
  120977. reactions
  120978. radicals
  120979. formation
  120980. te-bonds
  120981. reactions
  120982. ruclh
  120983. allylic
  120984. amines
  120985. insertions
  120986. reactions
  120987. ruthenium
  120988. carbenes
  120989. reactions
  120990. substituted
  120991. 2-butene-14-diyl
  120992. magnesium
  120993. complexe
  120994. reactions
  120995. sulfenic
  120996. sulfosylic
  120997. derivatives
  120998. reactions
  120999. sulfinyl
  121000. sulfonyl
  121001. carbanions
  121002. sulfenyla
  121003. reactions
  121004. atomic
  121005. oxygen
  121006. anion
  121007. synthes
  121008. reactions
  121009. eta-5-pyrrolyl
  121010. ligand
  121011. challenge
  121012. reactions
  121013. unsaturated
  121014. azides
  121015. direct
  121016. observation
  121017. reactions
  121018. vinyl
  121019. azides
  121020. reactions
  121021. vinylimino
  121022. phosphoranes
  121023. related
  121024. compounds
  121025. reactions
  121026. proceedin
  121027. cleavage
  121028. silicon-carbon
  121029. bonds
  121030. reactions
  121031. conservation
  121032. aromaticity
  121033. reactions
  121034. crown
  121035. ethers
  121036. reactions
  121037. aromaticity
  121038. reactions--reality
  121039. reactions-scope
  121040. reactiors
  121041. reactive
  121042. reactive
  121043. reactive
  121044. enolates
  121045. silyl
  121046. ethers
  121047. reactive
  121048. intermediates
  121049. interconversion
  121050. hydroc
  121051. reactive
  121052. organometallic
  121053. compounds
  121054. obtained
  121055. metallocenes
  121056. reactivit
  121057. reactivities
  121058. reactivityq
  121059. reactivity
  121060. reactivity
  121061. selectivity
  121062. lewis
  121063. acid-catalyzed
  121064. diels-ald
  121065. reactivity
  121066. stability
  121067. arenediazonium
  121068. reactivity
  121069. organic
  121070. chemistry
  121071. reactivity
  121072. arylidene
  121073. benzothiazinone
  121074. dioxides
  121075. reactivity
  121076. carbamoyl
  121077. radicals
  121078. first
  121079. general
  121080. conve
  121081. reactivity
  121082. carbon
  121083. anions
  121084. pentacooridinated
  121085. phosphoro
  121086. ylides
  121087. reactivity
  121088. five-membered
  121089. rings
  121090. heteroatom
  121091. reactivity
  121092. five-membered
  121093. rings
  121094. heteroato
  121095. reactivity
  121096. organic
  121097. compounds
  121098. water
  121099. geochemical
  121100. reactivity
  121101. hexacoordinate
  121102. silicon
  121103. compounds
  121104. reactivity
  121105. membered
  121106. rings
  121107. reactivity
  121108. small
  121109. large
  121110. rings
  121111. reactivity
  121112. substituted
  121113. aliphatic
  121114. nitro-compounds
  121115. reactivity-selectivi
  121116. reactor
  121117. reactors
  121118. readily
  121119. readily
  121120. available
  121121. chiral
  121122. carbon
  121123. fragments
  121124. their
  121125. readily
  121126. available
  121127. chromenone
  121128. receptors
  121129. carboxylates
  121130. reading
  121131. reaetion
  121132. reage
  121133. reagen
  121134. reagent
  121135. induced
  121136. substitution
  121137. reactions
  121138. reagent
  121139. control
  121140. aldol
  121141. addition
  121142. reaction
  121143. chiral
  121144. reagent
  121145. controlled
  121146. asymmetric
  121147. diels
  121148. alder
  121149. reactions
  121150. reagent
  121151. controlled
  121152. asymmetric
  121153. diels
  121154. alder
  121155. reactions
  121156. review
  121157. reagent
  121158. controlled
  121159. asymmetric
  121160. diels-alder
  121161. reactions
  121162. reagentsT
  121163. readily
  121164. available
  121165. chromenone
  121166. receptors
  121167. carboxylates@
  121168. reagent
  121169. catalysts
  121170. induced
  121171. substitution
  121172. reactions
  121173. meta@
  121174. reagents
  121175. realities@
  121176. rearrangement
  121177. rearrangement
  121178. tricyclic
  121179. series
  121180. synthesis
  121181. reactivity
  121182. hromi@
  121183. recent
  121184. advances
  121185. syntheses
  121186. crown
  121187. compounds@
  121188. recent
  121189. advances
  121190. reformatsky
  121191. reaction@
  121192. recent
  121193. advances
  121194. chemistry
  121195. chlorosulphonyl
  121196. isocyanat@
  121197. recent
  121198. aspects
  121199. chemistry
  121200. lactams
  121201. recent
  121202. developments
  121203. organic
  121204. synthesis
  121205. electrolysis@
  121206. recent
  121207. developments
  121208. stereoselective
  121209. synthesis
  121210. recent
  121211. developments
  121212. chemistry
  121213. thiocarbonyl
  121214. ylides@
  121215. recent
  121216. progress
  121217. chemistry
  121218. indole
  121219. alkaloids
  121220. recent
  121221. results
  121222. synthesis
  121223. semiochemicals
  121224. synthesis
  121225. receptors
  121226. reduction
  121227. reduction
  121228. metal
  121229. hydrides@
  121230. reduction
  121231. organic
  121232. diborane@
  121233. reagents
  121234. reagents
  121235. reagents
  121236. realm
  121237. rearranged
  121238. rearrangeme
  121239. rearrangementE
  121240. rearrangement
  121241. rearrangement
  121242. carbanions
  121243. rearrangement
  121244. rigid
  121245. cyclopropyl
  121246. carbinyl
  121247. radicals
  121248. detecti
  121249. rearrangement
  121250. studies
  121251. acylketene
  121252. methyl
  121253. rearrangement-cyclis
  121254. rearrangements
  121255. rearrangements
  121256. theoretical
  121257. approach
  121258. rearrangements
  121259. interconversions
  121260. carbenes
  121261. nitrenes
  121262. rearrangements
  121263. carbanions
  121264. rearrangements
  121265. organoboron
  121266. chemistry
  121267. rearrangements
  121268. involving
  121269. allenes
  121270. rearrangements
  121271. involving
  121272. boron
  121273. rearrangements
  121274. involving
  121275. carbonyl
  121276. group
  121277. rearrangements
  121278. benzene
  121279. derivatives
  121280. rearrangements
  121281. carbanions
  121282. rearrangements
  121283. carbenes
  121284. nitrenes
  121285. rearrangements
  121286. carbenes
  121287. nitrenes
  121288. rearrangements
  121289. carbocations
  121290. rearrangements
  121291. divinylcyclopropanes
  121292. rearrangements
  121293. epoxy
  121294. alcohols
  121295. related
  121296. compounds
  121297. rearrangements
  121298. alcohols
  121299. related
  121300. compounds
  121301. rearrangements
  121302. vinylcyclopropanes
  121303. related
  121304. systems
  121305. rearrangements/allyl
  121306. rearrangemment
  121307. rearrangemnt
  121308. rebeck
  121309. mechanistic
  121310. studies
  121311. using
  121312. solid
  121313. suppots
  121314. rebek
  121315. rebek
  121316. progress
  121317. development
  121318. epoxidation
  121319. recentq
  121320. recent
  121321. recent
  121322. recent
  121323. advanc
  121324. organoactinide
  121325. chemistry
  121326. recent
  121327. advance
  121328. synthesis
  121329. antibacterial
  121330. quinolines
  121331. recent
  121332. advances
  121333. arene
  121334. transformation
  121335. reactions
  121336. chromi
  121337. recent
  121338. advances
  121339. atropisomerism
  121340. recent
  121341. advances
  121342. azomethide
  121343. ylide
  121344. chemistry
  121345. recent
  121346. advances
  121347. azomethine
  121348. ylide
  121349. chemistry
  121350. recent
  121351. advances
  121352. carbon-carbon
  121353. forming
  121354. reactions
  121355. recent
  121356. advances
  121357. catalytic
  121358. antibodies
  121359. recent
  121360. advances
  121361. catalytic
  121362. asymmetri
  121363. reactions
  121364. promoted
  121365. recent
  121366. advances
  121367. catalytic
  121368. asymmetric
  121369. reactions
  121370. promoted
  121371. recent
  121372. advances
  121373. dianion
  121374. chemistry
  121375. recent
  121376. advances
  121377. double
  121378. formation
  121379. chira
  121380. recent
  121381. advances
  121382. fluoroheterocyclic
  121383. chemistry
  121384. recent
  121385. advances
  121386. glycosylation
  121387. reactions
  121388. recent
  121389. advances
  121390. halogenation
  121391. organic
  121392. compounds
  121393. recent
  121394. advances
  121395. isocyanate
  121396. chemistry
  121397. recent
  121398. advances
  121399. lactone
  121400. chemistry
  121401. recent
  121402. advances
  121403. o-quinodimet
  121404. chemistry
  121405. recent
  121406. advances
  121407. organolanthanide
  121408. chemistry
  121409. recent
  121410. advances
  121411. selected
  121412. aspects
  121413. bishomocubane
  121414. chemist
  121415. recent
  121416. advances
  121417. syntheses
  121418. crown
  121419. compounds
  121420. recent
  121421. advances
  121422. synthesis
  121423. pyrrolizidines
  121424. recent
  121425. advances
  121426. synthetic
  121427. applications
  121428. nitrile
  121429. oxide
  121430. recent
  121431. advances
  121432. asymmetric
  121433. dihydroxylation
  121434. alkenes
  121435. recent
  121436. advances
  121437. boron
  121438. route
  121439. asymmetric
  121440. synthe
  121441. recent
  121442. advances
  121443. boron
  121444. route
  121445. asymmetric
  121446. synthesis
  121447. recent
  121448. advances
  121449. chemistry
  121450. carborane
  121451. metal
  121452. complexe
  121453. recent
  121454. advances
  121455. chemistry
  121456. condensed
  121457. pyridazines
  121458. recent
  121459. advances
  121460. chemistry
  121461. conjugated
  121462. enamines
  121463. recent
  121464. advances
  121465. chemistry
  121466. homometallic
  121467. heterom
  121468. recent
  121469. advances
  121470. chemistry
  121471. lactam
  121472. antibiotics
  121473. recent
  121474. advances
  121475. chemistry
  121476. metal-carbon
  121477. triple
  121478. recent
  121479. advances
  121480. chemistry
  121481. unsaturated
  121482. lactones
  121483. recent
  121484. advances
  121485. cycloaddition
  121486. chemistry
  121487. isomunchno
  121488. recent
  121489. advances
  121490. preparation
  121491. synthetic
  121492. application
  121493. recent
  121494. advances
  121495. reformatsky
  121496. reaction
  121497. recent
  121498. advances
  121499. reformatsky
  121500. reaction
  121501. review
  121502. recent
  121503. advances
  121504. selective
  121505. formation
  121506. carbon-flu
  121507. recent
  121508. advances
  121509. staudinger
  121510. reaction
  121511. recent
  121512. advances
  121513. thetic
  121514. chlorocarbonyl
  121515. recent
  121516. advances
  121517. synthesis
  121518. achiral
  121519. carotenoids
  121520. recent
  121521. advances
  121522. synthesis
  121523. annelated
  121524. 14-benzodiazep
  121525. recent
  121526. advances
  121527. synthesis
  121528. phenothiazines
  121529. recent
  121530. advances
  121531. synthesis
  121532. pyrrolizidines
  121533. recent
  121534. advances
  121535. synthesis
  121536. vitamin
  121537. analogs
  121538. recent
  121539. advances
  121540. synthetic
  121541. chlorocarbonyl
  121542. recent
  121543. advances
  121544. total
  121545. synthesis
  121546. steroids
  121547. intra
  121548. recent
  121549. advances
  121550. acylium
  121551. salts
  121552. organic
  121553. synth
  121554. recent
  121555. advances
  121556. enzyme-catalysed
  121557. reactions
  121558. recent
  121559. advances
  121560. enzyme-catalyzed
  121561. reactions
  121562. recent
  121563. advances
  121564. thin-layer
  121565. chromatography
  121566. recent
  121567. advances
  121568. chemistry
  121569. chlorosulphonyl
  121570. isocyanat
  121571. recent
  121572. applications
  121573. alpha-metalated
  121574. isocyanides
  121575. organi
  121576. recent
  121577. applications
  121578. oxochromiumamine
  121579. complexes
  121580. oxidant
  121581. recent
  121582. applications
  121583. radical
  121584. reactions
  121585. natural
  121586. product
  121587. recent
  121588. applications
  121589. inverse
  121590. electron
  121591. demand
  121592. diels-ald
  121593. recent
  121594. applications
  121595. shanro
  121596. reaction
  121597. recent
  121598. applications
  121599. shapiro
  121600. reaction
  121601. recent
  121602. aspects
  121603. anthracyclinone
  121604. chemistry
  121605. recent
  121606. aspects
  121607. azirine
  121608. chemistry
  121609. recent
  121610. aspects
  121611. carbene
  121612. chemistry
  121613. recent
  121614. aspects
  121615. carbene
  121616. chemistry
  121617. review
  121618. recent
  121619. aspects
  121620. cyclopropanone
  121621. chemistry
  121622. recent
  121623. aspects
  121624. glycoconjugate
  121625. synthesis
  121626. synthetic
  121627. appro
  121628. recent
  121629. aspects
  121630. homolytic
  121631. aromatic
  121632. substitution
  121633. recent
  121634. aspects
  121635. organoselenium
  121636. chemistry
  121637. recent
  121638. aspects
  121639. singlet
  121640. oxygen
  121641. chemistry
  121642. photooxidation
  121643. recent
  121644. aspects
  121645. chemistry
  121646. lactams
  121647. recent
  121648. aspects
  121649. chemistry
  121650. lactams
  121651. recent
  121652. aspects
  121653. chemistry
  121654. lactams
  121655. recent
  121656. aspects
  121657. chemistry
  121658. nucleosides
  121659. nucleotides
  121660. recent
  121661. aspects
  121662. transition
  121663. metal
  121664. catalyzed
  121665. reactions
  121666. recent
  121667. contributions
  121668. kolbe
  121669. electrolysis
  121670. organic
  121671. synthe
  121672. recent
  121673. developmen
  121674. unsaturated
  121675. carbenes
  121676. related
  121677. recent
  121678. development
  121679. allene
  121680. chemistry
  121681. recent
  121682. development
  121683. carbodiimide
  121684. chemistry
  121685. recent
  121686. development
  121687. fluorin
  121688. agents
  121689. recent
  121690. development
  121691. fluorinating
  121692. agents
  121693. recent
  121694. developments
  121695. perspectives
  121696. reactio
  121697. recent
  121698. developments
  121699. allene
  121700. chemistry
  121701. recent
  121702. developments
  121703. asymmetric
  121704. aldol
  121705. methodology
  121706. recent
  121707. developments
  121708. carbodiimide
  121709. chemistry
  121710. recent
  121711. developments
  121712. chemical
  121713. deprotection
  121714. ester
  121715. functi
  121716. recent
  121717. developments
  121718. heterocyclic
  121719. systems
  121720. si-m'-ge
  121721. recent
  121722. developments
  121723. indole
  121724. synthesis
  121725. methodology
  121726. recent
  121727. developments
  121728. methods
  121729. ester
  121730. fication
  121731. recent
  121732. developments
  121733. organic
  121734. synthesis
  121735. electrolysis
  121736. recent
  121737. developments
  121738. organic
  121739. synthesis
  121740. liquid
  121741. sulfur
  121742. recent
  121743. developments
  121744. organic
  121745. synthesis
  121746. 1-haloalkyl
  121747. recent
  121748. developments
  121749. organic
  121750. synthesis
  121751. recent
  121752. developments
  121753. organocopper
  121754. chemistry
  121755. recent
  121756. developments
  121757. polycyclopentanoid
  121758. chemistry
  121759. recent
  121760. developments
  121761. stereoselective
  121762. aldol
  121763. reactions
  121764. recent
  121765. developments
  121766. sulfone
  121767. chemistry
  121768. recent
  121769. developments
  121770. tetrazole
  121771. chemistry
  121772. review
  121773. recent
  121774. developments
  121775. annulated
  121776. furans
  121777. recent
  121778. developments
  121779. annulated
  121780. furans
  121781. review
  121782. recent
  121783. developments
  121784. thionation
  121785. methods
  121786. recent
  121787. developments
  121788. birch
  121789. reduction
  121790. aromatic
  121791. compo
  121792. recent
  121793. developments
  121794. chemistry
  121795. cubane
  121796. recent
  121797. developments
  121798. stereoselective
  121799. synthesis
  121800. recent
  121801. developments
  121802. stereoselective
  121803. synthesis
  121804. recent
  121805. developments
  121806. stereoselective
  121807. synthesis
  121808. recent
  121809. developments
  121810. synthesis
  121811. chemistry
  121812. recent
  121813. developments
  121814. synthesis
  121815. aldehydes
  121816. reducti
  121817. recent
  121818. developments
  121819. synthesis
  121820. glycosides
  121821. recent
  121822. developments
  121823. synthesis
  121824. c-glycosides
  121825. recent
  121826. developments
  121827. synthesis
  121828. glycoconjugates
  121829. recent
  121830. developments
  121831. synthesis
  121832. macrolide
  121833. antibiotic
  121834. recent
  121835. developments
  121836. synthesis
  121837. medium-ring
  121838. ethers
  121839. recent
  121840. developments
  121841. synthesis
  121842. myo-inositol
  121843. phospha
  121844. recent
  121845. developments
  121846. synthesis
  121847. optically
  121848. active
  121849. recent
  121850. developments
  121851. synthesis
  121852. structure
  121853. chemistry
  121854. recent
  121855. developments
  121856. synthetic
  121857. applications
  121858. organoi
  121859. recent
  121860. developments
  121861. synthetic
  121862. chlorosulphonyl
  121863. recent
  121864. developments
  121865. silicon
  121866. organic
  121867. synthes
  121868. recent
  121869. developments
  121870. radical
  121871. substitutions
  121872. heteroa
  121873. recent
  121874. developments
  121875. chemistry
  121876. thiocarbonyl
  121877. ylides
  121878. recent
  121879. developments
  121880. protecting
  121881. groups
  121882. recent
  121883. eicosanoid
  121884. chemistry
  121885. recent
  121886. perspectives
  121887. concerning
  121888. mechanism
  121889. recent
  121890. progress
  121891. asymmetric
  121892. synthesis
  121893. pyrrolizidines
  121894. recent
  121895. progress
  121896. carotenoid
  121897. retinoid
  121898. synthesis
  121899. recent
  121900. progress
  121901. commercial
  121902. retinoids
  121903. carotenoids
  121904. recent
  121905. progress
  121906. erfluoroalkylation
  121907. radical
  121908. species
  121909. recent
  121910. progress
  121911. chemistry
  121912. acylsilanes
  121913. recent
  121914. progress
  121915. macrolide
  121916. synthesis
  121917. recent
  121918. progress
  121919. molecular
  121920. recognition
  121921. recent
  121922. progress
  121923. o-glycosylation
  121924. methods
  121925. applicati
  121926. recent
  121927. progress
  121928. quinoxaline
  121929. chemistry
  121930. synthesis
  121931. biolo
  121932. recent
  121933. progress
  121934. chemical
  121935. synthesis
  121936. antibiotics
  121937. recent
  121938. progress
  121939. chemical
  121940. synthesis
  121941. antibiotics
  121942. recent
  121943. progress
  121944. chemistry
  121945. acylsilanes
  121946. review
  121947. recent
  121948. progress
  121949. chemistry
  121950. indole
  121951. alkaloids
  121952. recent
  121953. progress
  121954. chemistry
  121955. indole
  121956. alkaloids
  121957. recent
  121958. progress
  121959. cycloaddition
  121960. reactions
  121961. oxido
  121962. recent
  121963. progress
  121964. enantioselective
  121965. synthesis
  121966. isoquin
  121967. recent
  121968. progress
  121969. preparation
  121970. synthetic
  121971. recent
  121972. progress
  121973. quinoxaline
  121974. chemistry
  121975. utility
  121976. recent
  121977. progress
  121978. synthesis
  121979. reactions
  121980. substitute
  121981. recent
  121982. progress
  121983. synthesis
  121984. reactivity
  121985. nitro
  121986. recent
  121987. progress
  121988. synthesis
  121989. reactivity
  121990. nitroketo
  121991. recent
  121992. progress
  121993. synthesis
  121994. avermectins
  121995. milbemyc
  121996. recent
  121997. progress
  121998. synthesis
  121999. butenolide
  122000. carotenoids
  122001. recent
  122002. progress
  122003. synthesis
  122004. taxanes
  122005. recent
  122006. progress
  122007. sulfonyl
  122008. radicals
  122009. organic
  122010. recent
  122011. results
  122012. spectroscopy
  122013. organolithium
  122014. compound
  122015. recent
  122016. results
  122017. field
  122018. asymmetric
  122019. synthesis
  122020. using
  122021. recent
  122022. results
  122023. synthesis
  122024. semiochemicals
  122025. synthesis
  122026. recent
  122027. review
  122028. synthesis
  122029. applications
  122030. silyl
  122031. recent
  122032. stereoselective
  122033. synthetic
  122034. approaches
  122035. amino
  122036. acids
  122037. recent
  122038. stereoselective
  122039. synthetic
  122040. approaches
  122041. beta-amino
  122042. recent
  122043. studies
  122044. carbocations
  122045. recent
  122046. studies
  122047. anomeric
  122048. effect
  122049. recent
  122050. studies
  122051. anomeric
  122052. effect
  122053. involvement
  122054. recent
  122055. studies
  122056. peterson
  122057. olefination
  122058. reaction
  122059. recent
  122060. studies
  122061. anomeric
  122062. effect
  122063. recent
  122064. studies
  122065. peterson
  122066. olefination
  122067. reaction
  122068. recent
  122069. synthetic
  122070. methods
  122071. polyfluoroaromatic
  122072. compounds
  122073. recent
  122074. synthetic
  122075. methods
  122076. pyrroles
  122077. pyrrolenines
  122078. recent
  122079. synthetic
  122080. methods
  122081. diazo
  122082. chemistry
  122083. recent
  122084. synthesis
  122085. phosphonate-containi
  122086. bone-ac
  122087. reception
  122088. receptor
  122089. receptorantagonists
  122090. receptors
  122091. receptors
  122092. rechthaler
  122093. recktenwal
  122094. recognition
  122095. recognitory
  122096. recognize
  122097. recognizing
  122098. recollections
  122099. recombinant
  122100. recommendations
  122101. recommended
  122102. recommended
  122103. methods
  122104. purification
  122105. solvents
  122106. reconciliation
  122107. rectangle
  122108. recueil
  122109. recurring
  122110. recyclisations
  122111. recyclizations
  122112. reddy
  122113. reden
  122114. reden
  122115. durckheimer
  122116. aminoglycoside
  122117. antibiotics
  122118. chemistry
  122119. rediel
  122120. redistribution
  122121. redox
  122122. redox
  122123. glycosidation
  122124. stereoselective
  122125. synthesis
  122126. sucrose
  122127. redpath
  122128. reducbon
  122129. reduced
  122130. reducing
  122131. reductants
  122132. reductase
  122133. reductases
  122134. reduction
  122135. reduction
  122136. reduction
  122137. related
  122138. reactions
  122139. alpha
  122140. unsaturated
  122141. reduction
  122142. related
  122143. reactions
  122144. alpha
  122145. beta-unsaturated
  122146. reduction
  122147. metal
  122148. alkoxyaluminum
  122149. hydrides
  122150. reduction
  122151. introduction
  122152. reduction
  122153. dissolving
  122154. metals
  122155. related
  122156. aacetals
  122157. thioacetals
  122158. ethers
  122159. reduction
  122160. alpha-substituted
  122161. carbonyl
  122162. compounds
  122163. cx-co
  122164. reduction
  122165. azides
  122166. borohydride
  122167. reduction
  122168. metal
  122169. hydrides
  122170. reduction
  122171. metal
  122172. hydrides
  122173. reduction
  122174. wolff-kishner
  122175. other
  122176. hydrazone
  122177. reduction
  122178. catalytic
  122179. hydrogenation
  122180. reduction
  122181. chirally
  122182. modified
  122183. hydride
  122184. reagen
  122185. reduction
  122186. dissolving
  122187. metals
  122188. related
  122189. reduction
  122190. hydride
  122191. delivery
  122192. carbon
  122193. reduction
  122194. electrolytically
  122195. reduction
  122196. using
  122197. enzymes
  122198. microorganisms
  122199. reduction
  122200. carboxylic
  122201. derivatives
  122202. alcohols
  122203. ethers
  122204. reduction
  122205. carboxylic
  122206. acids
  122207. aldehydes
  122208. metal
  122209. hydrides
  122210. reduction
  122211. carboxylic
  122212. acids
  122213. aldehydes
  122214. other
  122215. methods
  122216. reduction
  122217. diazo
  122218. hydroxy
  122219. esters
  122220. hydroxy
  122221. esters
  122222. includ
  122223. reduction
  122224. epoxides
  122225. reduction
  122226. imidoylstannanes
  122227. simple
  122228. method
  122229. prepar
  122230. reduction
  122231. ketones
  122232. alkenes
  122233. reduction
  122234. bonds
  122235. reduction
  122236. nitro
  122237. nitroso
  122238. compounds
  122239. reduction
  122240. organic
  122241. diborane
  122242. reduction
  122243. organic
  122244. compounds
  122245. alkoxyaluminohydride
  122246. reduction
  122247. organic
  122248. compounds
  122249. organotin
  122250. hydrides
  122251. reduction
  122252. organic
  122253. compounds
  122254. low-v
  122255. species
  122256. reduction
  122257. organic
  122258. compounds
  122259. sodium
  122260. aluminum
  122261. hydride
  122262. reduction
  122263. organic
  122264. functions
  122265. smi2-promoted
  122266. electron
  122267. reduction
  122268. reduction
  122269. saturated
  122270. alcohols
  122271. amines
  122272. alkanes
  122273. reduction
  122274. saturated
  122275. alkyl
  122276. halides
  122277. alkanes
  122278. reduction
  122279. sulfoxides
  122280. thioethers
  122281. reduction
  122282. sulfur-carbon
  122283. bonds
  122284. other
  122285. heteroatoms
  122286. reduction
  122287. vinyl
  122288. halides
  122289. alkenes
  122290. halides
  122291. reduction
  122292. aluminum
  122293. alkoxides
  122294. meerwein
  122295. ponndorf
  122296. reduction
  122297. aluminum
  122298. alkoxides
  122299. meerwein-ponndorf-ve
  122300. reduction
  122301. inorganic
  122302. reducing
  122303. agents
  122304. metal
  122305. carbonyls
  122306. reduction
  122307. inorganic
  122308. reducing
  122309. agents
  122310. metal
  122311. hydrides
  122312. reduction
  122313. inorganic
  122314. reducing
  122315. agents
  122316. metal
  122317. salts
  122318. reduction
  122319. inorganic
  122320. reducing
  122321. agents
  122322. metals
  122323. reduction
  122324. inorganic
  122325. reducing
  122326. agents
  122327. metals
  122328. reduction
  122329. organic
  122330. compounds
  122331. reduction
  122332. organometallic
  122333. compounds
  122334. reduction
  122335. samarium
  122336. debromination
  122337. dibromides
  122338. reductions
  122339. tions
  122340. radical
  122341. cyclizations
  122342. alkyl
  122343. bromid
  122344. reductions
  122345. lithium
  122346. aluminum
  122347. hydride
  122348. reductions
  122349. lithium
  122350. aluminum
  122351. hydride
  122352. weldon
  122353. brown
  122354. organi
  122355. reductions
  122356. metal
  122357. alkoxyaluminum
  122358. hydrides
  122359. carboxyl
  122360. reductions
  122361. alumino
  122362. borohydrides
  122363. organic
  122364. synthe
  122365. reductions
  122366. alkynes
  122367. noncatalytic
  122368. chemical
  122369. metho
  122370. reduction
  122371. inorganic
  122372. reducing
  122373. agents
  122374. metal
  122375. salts@
  122376. reductions
  122377. radical
  122378. cyclizations
  122379. alkyl
  122380. bromid@
  122381. reductions
  122382. cyclic
  122383. bicyclic
  122384. ketones
  122385. complex
  122386. metal
  122387. reductive
  122388. cyclization
  122389. ketones
  122390. tethered
  122391. activated
  122392. olefi@
  122393. reetz
  122394. metal
  122395. ligand
  122396. protective
  122397. group
  122398. tuning
  122399. mean@
  122400. reflections
  122401. complex
  122402. theory
  122403. benzidine
  122404. rearrangement@
  122405. regio
  122406. stereochemical
  122407. variations
  122408. diels
  122409. alder
  122410. reactions@
  122411. regiose
  122412. ective
  122413. manipulation
  122414. hydroxyl
  122415. groups
  122416. organotin@
  122417. regioselective
  122418. cross
  122419. coupling
  122420. reaction
  122421. phenylthioethynyl
  122422. regioselective
  122423. prenylation
  122424. phenols
  122425. palladium
  122426. catalyst
  122427. reider@
  122428. related
  122429. relatet@
  122430. relationship
  122431. remarkable
  122432. selectivity
  122433. reaction
  122434. trityl
  122435. lithioi@
  122436. remarkably@
  122437. repair@
  122438. reports
  122439. intermediates
  122440. structure
  122441. spectroscopy
  122442. research
  122443. resonance
  122444. boron@
  122445. review
  122446. reductions
  122447. cyclic
  122448. bicyclic
  122449. ketones
  122450. complex
  122451. metal
  122452. reductions
  122453. functional
  122454. groups
  122455. sulfurated
  122456. borohydrides
  122457. reductions
  122458. promoted
  122459. valent
  122460. transition
  122461. metal
  122462. complexes
  122463. reductions
  122464. chiral
  122465. boron
  122466. reagents
  122467. reductions
  122468. chiral
  122469. dihydropyridine
  122470. reagents
  122471. reductions
  122472. chiral
  122473. modifications
  122474. lithium
  122475. aluminium
  122476. reductions
  122477. samarium
  122478. iodide
  122479. reductive
  122480. reductive
  122481. cleavage
  122482. aliphatic
  122483. nitro
  122484. groups
  122485. organic
  122486. reductive
  122487. cleavage
  122488. groups
  122489. under
  122490. neutral
  122491. conditions
  122492. reductive
  122493. cupration
  122494. cyanoketene
  122495. dithioacetals
  122496. generation
  122497. reductive
  122498. cyclization
  122499. enones
  122500. titanium
  122501. catalyst
  122502. reductive
  122503. cyclization
  122504. ketones
  122505. tethered
  122506. activated
  122507. olefi
  122508. reductive
  122509. dehalogenation
  122510. polyhalo
  122511. ketones
  122512. low-valent
  122513. reductive
  122514. deprotection
  122515. allyl
  122516. ethers
  122517. reductive
  122518. elimination
  122519. vicinal
  122520. deoxygenation
  122521. vicinal
  122522. reductive
  122523. lithiation
  122524. phenylsulfones
  122525. reductive
  122526. lithiation
  122527. halopyridines
  122528. using
  122529. lithium
  122530. naphthal
  122531. reductive
  122532. trans
  122533. diallylation
  122534. aromatic
  122535. reductive
  122536. rearrangement
  122537. nitrobicyclo
  122538. 2.2.1
  122539. reductive
  122540. thiation
  122541. diepoxides
  122542. lithioalkoxides
  122543. chemistry
  122544. benzazetes
  122545. trends
  122546. charles
  122547. polysulfur
  122548. nitrogen
  122549. heterocyclic
  122550. chemistry
  122551. reese
  122552. reese
  122553. chemical
  122554. synthesis
  122555. oligo
  122556. nucleotid
  122557. reetz
  122558. reetz
  122559. anchimerically
  122560. accelerated
  122561. homolyses
  122562. 197918
  122563. reetz
  122564. metal
  122565. ligand
  122566. protective
  122567. group
  122568. tuning
  122569. reetz
  122570. manfred
  122571. approaches
  122572. amino
  122573. acids
  122574. reevaluation
  122575. reexamination
  122576. reexamined
  122577. referenccs
  122578. reference
  122579. references
  122580. reflections
  122581. reflections
  122582. carotenoid
  122583. synthesis
  122584. reflections
  122585. organic
  122586. synthesis
  122587. evolution
  122588. general
  122589. reflections
  122590. complex
  122591. theory
  122592. benzidine
  122593. rearrangement
  122594. reformatsky
  122595. regarding
  122596. regen
  122597. regen
  122598. triphase
  122599. catalysis
  122600. 197918
  122601. angewandte
  122602. chemie
  122603. regenerable
  122604. regeneration
  122605. reger
  122606. reger
  122607. daniel
  122608. pyrazolyl
  122609. borate
  122610. complexes
  122611. specific
  122612. stereospecific
  122613. introduction
  122614. azide
  122615. funct
  122616. regina
  122617. reginald
  122618. reginato
  122619. regio
  122620. regio
  122621. chemoselective
  122622. synthesis
  122623. halohydrins
  122624. cleavag
  122625. regio
  122626. enantiocontrolled
  122627. addition
  122628. organoaluminium
  122629. regio
  122630. enantioselective
  122631. silane
  122632. terminated
  122633. intramolecular
  122634. regio
  122635. stereochemical
  122636. control
  122637. substitution
  122638. reactions
  122639. regio
  122640. stereochemical
  122641. variations
  122642. diels
  122643. alder
  122644. reactions
  122645. regio
  122646. stereocontrolled
  122647. catalytic
  122648. palladium
  122649. nickel
  122650. regio
  122651. stereoselective
  122652. synthesis
  122653. methyl
  122654. alkenylt
  122655. regio
  122656. stereoselective
  122657. synthesis
  122658. isoxazolidines
  122659. bearin
  122660. regio
  122661. stereoselective
  122662. synthesis
  122663. unsaturated
  122664. carbonyl
  122665. regio
  122666. stereoselectivity
  122667. mediated
  122668. addition
  122669. regio-and
  122670. regiochemical
  122671. regiochemical
  122672. control
  122673. opening
  122674. epoxides
  122675. regiochemically
  122676. regiochemically
  122677. stereochemically
  122678. defined
  122679. synthesis
  122680. regiochemistry
  122681. regiocontrol
  122682. regiocontrol
  122683. remote
  122684. substituents
  122685. direct
  122686. total
  122687. synthesis
  122688. regiocontrol
  122689. copper
  122690. catalyzed
  122691. cross
  122692. coupling
  122693. allylic
  122694. regiocontrolled
  122695. regiocontrolled
  122696. total
  122697. synthesis
  122698. imerubrine
  122699. first
  122700. region
  122701. regions
  122702. regiose
  122703. regiose
  122704. ective
  122705. manipulation
  122706. hydroxyl
  122707. groups
  122708. organotin
  122709. regioselection
  122710. regioselective
  122711. regioselective
  122712. chlorination
  122713. benzodiazepine
  122714. analogu
  122715. regioselective
  122716. addition
  122717. stannylcyanocuprates
  122718. acetyleni
  122719. regioselective
  122720. allylation
  122721. silyl
  122722. ethers
  122723. hetero
  122724. regioselective
  122725. diastereoselective
  122726. synthesis
  122727. stannyl
  122728. regioselective
  122729. endo-stereoselective
  122730. cycoaddition
  122731. regioselective
  122732. cases
  122733. stereoselective
  122734. carbonylati
  122735. regioselective
  122736. stereospecific
  122737. formation
  122738. ethynyl
  122739. regioselective
  122740. radical
  122741. cyclization
  122742. stereocontrolled
  122743. regioselective
  122744. cross
  122745. coupling
  122746. reaction
  122747. phenylthioethynyl
  122748. regioselective
  122749. formation
  122750. allylidenecyclopropa
  122751. fische
  122752. regioselective
  122753. hydroformylation
  122754. alkenes
  122755. catalyzed
  122756. regioselective
  122757. methods
  122758. synthesis
  122759. asymmetrically
  122760. substi
  122761. regioselective
  122762. methyl
  122763. carbon
  122764. lithiation
  122765. methylalk
  122766. regioselective
  122767. olefin
  122768. insertion
  122769. asymmetric
  122770. reaction
  122771. regioselective
  122772. opening
  122773. terminal
  122774. epoxides
  122775. trialkyls
  122776. regioselective
  122777. oxidative
  122778. cleavage
  122779. functionalized
  122780. unsymmet
  122781. regioselective
  122782. palladium
  122783. catalyzed
  122784. hydrostannylation
  122785. selective
  122786. prenylation
  122787. phenols
  122788. palladium
  122789. catalyst
  122790. regioselective
  122791. promoted
  122792. reactions
  122793. methyl
  122794. diazoa
  122795. regioselective
  122796. opening
  122797. silyl
  122798. epoxy
  122799. alcohols
  122800. regioselective
  122801. substitution
  122802. aromatic
  122803. membered
  122804. nitroge
  122805. regioselective
  122806. substitution
  122807. aromatic
  122808. six-membered
  122809. nitroge
  122810. regioselective
  122811. synthesis
  122812. alkenyl
  122813. sulfides
  122814. alkenyl
  122815. regioselective
  122816. synthetic
  122817. processes
  122818. based
  122819. aromatic
  122820. regioselectively
  122821. regioselectivities
  122822. regioselectivity
  122823. regioselectivity
  122824. stereoselectivity
  122825. radical
  122826. reactions
  122827. regioselectivity
  122828. stereoselectivity
  122829. intramolecular
  122830. regioselectivity
  122831. diels
  122832. alder
  122833. reactions
  122834. regioselectivity
  122835. singlet
  122836. oxygen
  122837. reaction
  122838. schenck
  122839. regioselectivity
  122840. stereoselectivity
  122841. enantioselectivity
  122842. regiospecific
  122843. specific
  122844. alkylation
  122845. cyclohexenones
  122846. review
  122847. regiospecific
  122848. procedure
  122849. preparation
  122850. silyl
  122851. regiospecific
  122852. synthesis
  122853. disubstituted
  122854. furans
  122855. regiosp
  122856. regiospecific
  122857. synthesis
  122858. amino
  122859. acetals
  122860. dialkoxy
  122861. regiospecifically
  122862. regiospecificty
  122863. regiospecificty
  122864. cyclization
  122865. 1-hydroxyalkyl
  122866. geran
  122867. register
  122868. regitz
  122869. regular
  122870. regulation
  122871. regulatory
  122872. rehacek
  122873. rehorek
  122874. rehorek
  122875. detlef
  122876. trapping
  122877. inorganic
  122878. radicals
  122879. chemical
  122880. reich
  122881. reich
  122882. functional
  122883. group
  122884. manipulation
  122885. using
  122886. organoselenium
  122887. reich
  122888. organoselenium
  122889. oxidations
  122890. oxidation
  122891. organic
  122892. reichardt
  122893. reichardt
  122894. solvatochromism
  122895. thermochromism
  122896. piezochromism
  122897. reichardt
  122898. empirical
  122899. parameters
  122900. solvent
  122901. polarity
  122902. reichardt
  122903. solvent
  122904. effects
  122905. organic
  122906. chemistry
  122907. monograph
  122908. reichen
  122909. reichen
  122910. oxygen
  122911. nitrogen
  122912. sulfur
  122913. substituted
  122914. heteroallen
  122915. reichert
  122916. reichert
  122917. toxication
  122918. foreign
  122919. substances
  122920. conjugation
  122921. reidel
  122922. reider
  122923. reiko
  122924. reilly
  122925. reimer
  122926. reimer-tiemann
  122927. reimschussel
  122928. reinecke
  122929. reiner
  122930. reinhard
  122931. reinhardt
  122932. reinhart
  122933. reinhold
  122934. reinhoudt
  122935. reinhoudt
  122936. crown
  122937. ethers
  122938. related
  122939. macrocycles
  122940. reinvestigation
  122941. reinvestigation
  122942. modified
  122943. hantzsch
  122944. thiazole
  122945. synthesis
  122946. reinvestigation
  122947. lewis
  122948. mediated
  122949. reaction
  122950. reinvestigation
  122951. oxidative
  122952. rearrangement
  122953. yohimbane
  122954. reiser
  122955. reiser
  122956. oliver
  122957. palladium
  122958. catalyzed
  122959. enantioselective
  122960. allylic
  122961. reiser
  122962. olivier
  122963. oxidation
  122964. weakly
  122965. activatedc
  122966. bonds
  122967. angewa
  122968. reissert
  122969. reissig
  122970. reissig
  122971. ulrich
  122972. sugars
  122973. chiral
  122974. auxiliaries
  122975. reitz
  122976. relatedC
  122977. related
  122978. related
  122979. relation
  122980. relations
  122981. relations
  122982. between
  122983. structure
  122984. ivity
  122985. free-radical
  122986. relationship
  122987. relationship
  122988. relationships
  122989. relative
  122990. relative
  122991. rates
  122992. cycloaromatization
  122993. dynemicin
  122994. azabicyclo
  122995. relative
  122996. reactivities
  122997. double
  122998. triple
  122999. bonds
  123000. towards
  123001. relatives
  123002. relaxation
  123003. release
  123004. releasers
  123005. relevance
  123006. relevance
  123007. conformational
  123008. constraints
  123009. regioselectiv
  123010. relevant
  123011. relevent
  123012. reliable
  123013. remarkable
  123014. rkable
  123015. selectivity
  123016. reaction
  123017. trityl
  123018. lithioi
  123019. remarkably
  123020. remers
  123021. remers
  123022. indole
  123023. aldehydes
  123024. ketones
  123025. chemistry
  123026. remers
  123027. chemistry
  123028. antitumor
  123029. antibiotics
  123030. remnud
  123031. remote
  123032. remote
  123033. acyclic
  123034. diastereocontrol
  123035. involving
  123036. bicyclic
  123037. metal
  123038. remote
  123039. asymmetric
  123040. induction
  123041. using
  123042. allylstannanes
  123043. remote
  123044. asymmetric
  123045. induction
  123046. using
  123047. neighboring
  123048. group
  123049. particip
  123050. remote
  123051. carbonylation
  123052. synthesis
  123053. g-lactones
  123054. satura
  123055. remote
  123056. functionalisation
  123057. bonds
  123058. naked
  123059. trans
  123060. removable
  123061. removal
  123062. renaissance
  123063. renard
  123064. renations
  123065. renato
  123066. renctions
  123067. renee
  123068. renfroe
  123069. renji
  123070. renuka
  123071. reorganization
  123072. reorganizations
  123073. reoselective
  123074. repair
  123075. reparative
  123076. reparative
  123077. flash-vacuum
  123078. thermolysis
  123079. revival
  123080. pyrolytic
  123081. repke
  123082. replacement
  123083. replacement
  123084. alcoholic
  123085. hydroxyl
  123086. groups
  123087. halogens
  123088. replacement
  123089. aromatic
  123090. primary
  123091. amino
  123092. group
  123093. hydrogen
  123094. replacement
  123095. aromatic
  123096. primary
  123097. amino
  123098. group
  123099. hydrogen
  123100. replacements
  123101. replacing
  123102. replicating
  123103. replication
  123104. replication
  123105. assembly
  123106. report
  123107. reports
  123108. reports
  123109. representation
  123110. representative
  123111. representitive
  123112. republic
  123113. repulsive
  123114. requirement
  123115. requirements
  123116. intermediates
  123117. modern
  123118. methods
  123119. intermediates
  123120. photochemistry
  123121. photophy
  123122. intermediates
  123123. structure
  123124. spectroscopy
  123125. resctions
  123126. research
  123127. research
  123128. research
  123129. research1994
  123130. researches
  123131. resemble
  123132. reservoirs
  123133. reshetova
  123134. reshetova
  123135. tkhaper
  123136. kamernitskii
  123137. progress
  123138. reshuffling
  123139. reshuffling
  123140. functionalities
  123141. catalyzed
  123142. ruthenium
  123143. resin
  123144. resins
  123145. resinsulfonic
  123146. resinsulphonic
  123147. resistance
  123148. resnati
  123149. resnati
  123150. giuseppe
  123151. synthesis
  123152. chiral
  123153. bioactive
  123154. fluoroorg
  123155. resolution
  123156. compo
  123157. resolutions
  123158. resolved
  123159. resolving
  123160. resonance
  123161. resonance
  123162. resonances
  123163. resorcinol
  123164. response
  123165. responsible
  123166. restricted
  123167. restriction
  123168. result
  123169. resultant
  123170. resulting
  123171. results
  123172. retated
  123173. retention
  123174. retention
  123175. configuration
  123176. ritter
  123177. substitution
  123178. retero
  123179. retey
  123180. retherford
  123181. rethwisch
  123182. retigeranic
  123183. retinal
  123184. retinals
  123185. retinoid
  123186. retinoids
  123187. retrieval
  123188. retro
  123189. retro-arbuzov
  123190. retro-ene
  123191. retroaddition
  123192. retrograde
  123193. retrograde
  123194. diels-alder
  123195. reactions
  123196. retronecine
  123197. retronecine
  123198. retrospect
  123199. retrospective
  123200. retrosynthesis
  123201. retrosynthesis
  123202. heterocycles
  123203. retrosynthetic
  123204. retrosynthetic
  123205. thinking
  123206. essentials
  123207. examples
  123208. rettig
  123209. rettig
  123210. wolfgang
  123211. photoinduced
  123212. charge
  123213. separation
  123214. twisted
  123215. return
  123216. reuben
  123217. reuck
  123218. reuman
  123219. reutov
  123220. reutov
  123221. beletskaya
  123222. butin
  123223. acids
  123224. pergamon
  123225. press
  123226. reutov
  123227. kurts
  123228. advances
  123229. chemistry
  123230. ambident
  123231. reutov
  123232. aspects
  123233. organometallic
  123234. chemistry
  123235. nontr
  123236. reveal
  123237. revealed
  123238. revealing
  123239. reveals
  123240. reversable
  123241. reversal
  123242. reversal
  123243. regiochemistry
  123244. synthesis
  123245. isoxazoles
  123246. reversal
  123247. stereoselectivity
  123248. aldol
  123249. reaction
  123250. boron
  123251. reverse
  123252. reverse
  123253. chemoselectivity
  123254. competitive
  123255. addition
  123256. reversed
  123257. reverses
  123258. reversibility
  123259. reversible
  123260. reversible-reactions
  123261. reversing
  123262. reversing
  123263. regiochemical
  123264. course
  123265. dipolar
  123266. cycloadditi
  123267. reviewC
  123268. review
  123269. review
  123270. review
  123271. arene
  123272. synthesis
  123273. extrusion
  123274. heteroatoms
  123275. review
  123276. synthesis
  123277. conjugated
  123278. lactones@
  123279. reviews
  123280. reviews
  123281. samarium
  123282. chemistry@
  123283. rh-mediated@
  123284. rhodium
  123285. catalysed
  123286. coupling
  123287. reactions
  123288. involving
  123289. open@
  123290. rhodium-vinylallene@
  123291. ricci@
  123292. carbodiimide
  123293. method
  123294. peptides
  123295. sugar
  123296. mimics
  123297. potential
  123298. infectives
  123299. rodin@
  123300. rokhlin@
  123301. iodide
  123302. sequence-selective
  123303. cleavage
  123304. bjoern
  123305. serrano
  123306. andres
  123307. merchan
  123308. manuela
  123309. multiconfi@
  123310. rotenoids
  123311. their
  123312. biosynthesis
  123313. route
  123314. review
  123315. review
  123316. review
  123317. review
  123318. review
  123319. review
  123320. review
  123321. review
  123322. review
  123323. review
  123324. review
  123325. review
  123326. review
  123327. review
  123328. review
  123329. review
  123330. review
  123331. review
  123332. review
  123333. review
  123334. review
  123335. review
  123336. review
  123337. review
  123338. review
  123339. review
  123340. review
  123341. review
  123342. review
  123343. review
  123344. review
  123345. review
  123346. review
  123347. review
  123348. review
  123349. review
  123350. asymmetric
  123351. synthesis
  123352. industrial
  123353. prospect
  123354. review
  123355. conversion
  123356. primary
  123357. amino
  123358. groups
  123359. other
  123360. functio
  123361. review
  123362. dealing
  123363. synthesis
  123364. lactams
  123365. review
  123366. hererocyclic
  123367. amidines
  123368. hydroxyamidines
  123369. synthons
  123370. review
  123371. literature
  123372. heterocycles
  123373. review
  123374. acetylene
  123375. equivalents
  123376. cycloaddition
  123377. reactions
  123378. review
  123379. arene
  123380. synthesis
  123381. extrusion
  123382. heteroatoms
  123383. review
  123384. asymmetric
  123385. reduction
  123386. carbonyl
  123387. groups
  123388. boron
  123389. review
  123390. chemistry
  123391. formamide
  123392. acetals
  123393. review
  123394. review
  123395. lewis
  123396. desilylation
  123397. synthesis
  123398. review
  123399. methods
  123400. esterification
  123401. protection
  123402. review
  123403. mitomycin
  123404. behavior
  123405. biological
  123406. justification
  123407. review
  123408. acyliminium
  123409. cyclizations
  123410. stereoselectivi
  123411. review
  123412. phase
  123413. transfer
  123414. catalysts
  123415. review
  123416. pyrolizidine
  123417. alkaloid
  123418. synthesis
  123419. using
  123420. intramol
  123421. review
  123422. chemistry
  123423. sulfonyl
  123424. carbanion
  123425. alkylation
  123426. review
  123427. mitsunobu
  123428. reaction
  123429. involving
  123430. triphenyl
  123431. phosphi
  123432. review
  123433. transition
  123434. metal
  123435. catalyzed
  123436. selective
  123437. organic
  123438. react
  123439. review
  123440. olefin
  123441. inversion
  123442. review
  123443. dipolar
  123444. cycloreversion
  123445. review
  123446. aldol
  123447. chemistry
  123448. borinates
  123449. review
  123450. chemistry
  123451. conjugated
  123452. enamines
  123453. review
  123454. hindered
  123455. amines
  123456. piperidines
  123457. review
  123458. synthesis
  123459. conjugated
  123460. lactones
  123461. review
  123462. recent
  123463. developments
  123464. chemistry
  123465. ylidene
  123466. azolo
  123467. reviews
  123468. reviews
  123469. reviews
  123470. reviews
  123471. reviews
  123472. reviews
  123473. samarium
  123474. chemistry
  123475. reviews
  123476. borane
  123477. chemistry
  123478. revisedQ
  123479. revision
  123480. revisite
  123481. revisited
  123482. revival
  123483. reward
  123484. rewcastle
  123485. rewcatle
  123486. rewcatle
  123487. gordon
  123488. katritzky
  123489. generation
  123490. reactions
  123491. rey's
  123492. reyes
  123493. reynold
  123494. reynolds
  123495. reznikovJ
  123496. rezno
  123497. rganic
  123498. rganometallic
  123499. rganosulfur-silicon
  123500. rh-catalyzed
  123501. rheingold
  123502. rhenium
  123503. rhizopus
  123504. rhizoxin
  123505. rhoads
  123506. rhodes
  123507. rhodium
  123508. rhodium
  123509. catalysed
  123510. coupling
  123511. reactions
  123512. involving
  123513. rhodium
  123514. catalysed
  123515. hydroamination
  123516. hydroarylation
  123517. norbornen
  123518. rhodium
  123519. catalyzed
  123520. cross
  123521. coupling
  123522. unactivated
  123523. allenes
  123524. rhodium
  123525. catalysed
  123526. hydroboration
  123527. alkenes
  123528. rhodium
  123529. carboxylates
  123530. rhodium
  123531. catalyzed
  123532. intramolecular
  123533. reactions
  123534. between
  123535. vinyl
  123536. rhodium
  123537. catalyzed
  123538. intramolecular
  123539. reactions
  123540. between
  123541. vinyld
  123542. rhodium
  123543. catalyzed
  123544. reactions
  123545. diazo-carbonyl
  123546. compounds
  123547. rhodium-catalyzed
  123548. rhodium-catalyzed
  123549. alkyne
  123550. cyclotrimerization
  123551. strategies
  123552. rhodium-catalyzed
  123553. carbonylation
  123554. 2-alkynlaniline
  123555. synthesis
  123556. rhodium-catalyzed
  123557. hydroboration
  123558. rhodium-catalyzed
  123559. hydroformylation
  123560. internal
  123561. alkynes
  123562. psins
  123563. rhythms
  123564. riant
  123565. ribbons
  123566. ribereau
  123567. ribofuranose
  123568. ribonolactone
  123569. ribonucleic
  123570. ribonucleotides
  123571. ribosomal
  123572. ribot
  123573. ricca
  123574. ricci
  123575. ricci
  123576. reginato
  123577. degl'innocenti
  123578. seconi
  123579. organometallic
  123580. ricco
  123581. carbodiimide
  123582. method
  123583. peptides
  123584. richard
  123585. richards
  123586. richards
  123587. computer
  123588. aided
  123589. design
  123590. richardson
  123591. richer
  123592. richmond
  123593. richter
  123594. rickborn
  123595. diffusion
  123596. control
  123597. association
  123598. nitrosatio
  123599. range
  123600. radical
  123601. processes
  123602. nitration
  123603. riddell
  123604. riddell
  123605. conformational
  123606. analysis
  123607. heterocyclic
  123608. riddell
  123609. conformations
  123610. hydroxylamine
  123611. derivatives
  123612. rideout
  123613. riechstoffe
  123614. riediker
  123615. riehard
  123616. rieke
  123617. rieker
  123618. riera
  123619. riess
  123620. riess
  123621. blanc
  123622. perfluoro
  123623. compounds
  123624. blood
  123625. substitute
  123626. rifaat
  123627. riffle
  123628. rigby
  123629. rigby
  123630. james
  123631. transition
  123632. metal
  123633. promoted
  123634. higher
  123635. order
  123636. cycload
  123637. righi
  123638. right
  123639. right
  123640. left--this
  123641. question
  123642. enantioselective
  123643. catalys
  123644. rigid
  123645. rigid
  123646. highly
  123647. enantioselective
  123648. catalyst
  123649. dihydroxy
  123650. rigid
  123651. molecular
  123652. tweezers
  123653. hosts
  123654. complexation
  123655. rigidly
  123656. rijke
  123657. rilling
  123658. rimoldi
  123659. rinaldi
  123660. rinaldo
  123661. rinehart
  123662. ring]
  123663. chain
  123664. transformations
  123665. semicyclic
  123666. chloropropenimini
  123667. cleavage
  123668. benzofurans
  123669. tetrahydrobenzofuran
  123670. closing
  123671. metathesis
  123672. related
  123673. processes
  123674. organic
  123675. closure
  123676. methods
  123677. synthesis
  123678. macrocyclic
  123679. natural
  123680. closure
  123681. reactions
  123682. bifunctional
  123683. chain
  123684. molecules
  123685. contractions
  123686. expansions
  123687. vicinally
  123688. disubstituted
  123689. contractions
  123690. carbohydrates
  123691. enlargement
  123692. organic
  123693. chemistry
  123694. formation
  123695. through
  123696. intramolecular
  123697. displacement
  123698. opening
  123699. reactions
  123700. oxabicyclic
  123701. compounds
  123702. route
  123703. opening
  123704. reactions
  123705. alpha
  123706. stannyl
  123707. epoxides
  123708. metal
  123709. selective
  123710. syntheses
  123711. homochiral
  123712. oxepanes
  123713. tetrahyd
  123714. transformation
  123715. heterocycles
  123716. conversion
  123717. transformations
  123718. five-membered
  123719. heterocycles
  123720. ring-cleavage
  123721. ring-closing
  123722. ring-fused
  123723. ring-opening
  123724. ring-opening
  123725. five-membered
  123726. heteroaromatic
  123727. azides
  123728. rings
  123729. rings
  123730. radicals
  123731. synthetic
  123732. metals
  123733. chemistry
  123734. ripka
  123735. ripoll
  123736. ripoll
  123737. rouessac
  123738. recent
  123739. applications
  123740. diels
  123741. alder
  123742. ripperger
  123743. ripperger
  123744. schreiber
  123745. solanum
  123746. steroid
  123747. alkaloids
  123748. alkalo
  123749. ritter
  123750. ritter
  123751. synthetic
  123752. transformations
  123753. vinyl
  123754. ritter
  123755. reactions
  123756. transannular
  123757. addition
  123758. nitriles
  123759. ritter-type
  123760. ritter-type
  123761. reactions
  123762. rivalry
  123763. rivarola
  123764. rivatives
  123765. rivett
  123766. rivier
  123767. abdel
  123768. fattah
  123769. naturally
  123770. occurring
  123771. review
  123772. abdel
  123773. fattah
  123774. naturally
  123775. occurring
  123776. pyrrolizidine
  123777. rizzi
  123778. roald
  123779. robert
  123780. roberta
  123781. robertj
  123782. roberto
  123783. roberts
  123784. roberts
  123785. chemistry
  123786. phosphoranyl
  123787. radicals
  123788. advances
  123789. roberts
  123790. right
  123791. place
  123792. right
  123793. profiles
  123794. roberts
  123795. photoelectron
  123796. spectroscopy
  123797. surface
  123798. chemistry
  123799. roberts
  123800. gibson
  123801. applications
  123802. isotopic
  123803. labeling
  123804. roberts
  123805. exploitation
  123806. microbiological
  123807. methods
  123808. roberts
  123809. enzymes
  123810. catalysis
  123811. roberts
  123812. stanley
  123813. sugar
  123814. mimics
  123815. potential
  123816. infectives
  123817. roberts
  123818. stanley
  123819. sugar
  123820. mimics
  123821. potential
  123822. infectives
  123823. robertson
  123824. robin
  123825. robins
  123826. robins
  123827. advances
  123828. pyrrolizidine
  123829. chemistry
  123830. robins
  123831. pyrrolizidine
  123832. alkaloids
  123833. natural
  123834. robins
  123835. pyrrolizidine
  123836. alkaloids
  123837. natural
  123838. robins
  123839. pyrrolizidine
  123840. alkaloids
  123841. natural
  123842. product
  123843. reports
  123844. robins
  123845. richard
  123846. walton
  123847. nicholas
  123848. biosynthesis
  123849. tropa
  123850. robinson
  123851. robinson
  123852. chemical
  123853. biological
  123854. aspects
  123855. polyether
  123856. roboz
  123857. roboz
  123858. diagnosis
  123859. monitoring
  123860. disseminated
  123861. candidiasis
  123862. robust
  123863. rocarbon
  123864. rocchi
  123865. rocha
  123866. rocket
  123867. rockett
  123868. rodanes
  123869. rodd'sW
  123870. rodin
  123871. rodionov
  123872. rodionov
  123873. furin
  123874. kinetics
  123875. nucleophilic
  123876. substitution
  123877. rodney
  123878. rodrigo
  123879. rodriguez
  123880. rodriguez
  123881. dulcere
  123882. pierre
  123883. cohalogenation
  123884. organic
  123885. roegesL
  123886. roeges
  123887. guide
  123888. complete
  123889. interpretation
  123890. infraL
  123891. roeske
  123892. roesky
  123893. roesky
  123894. herbert
  123895. chemistry
  123896. without
  123897. borders
  123898. between
  123899. rofer
  123900. rofer
  123901. depoorter
  123902. comprehensive
  123903. mechanism
  123904. fische
  123905. roflamycoin
  123906. rogan
  123907. rogan
  123908. altria
  123909. goodall
  123910. enantioselective
  123911. separation
  123912. roger
  123913. rogers
  123914. rogic
  123915. rogic
  123916. demmin
  123917. copper
  123918. induced
  123919. oxygenolysis
  123920. rogozhin
  123921. rohmer
  123922. thiericke
  123923. angucycline
  123924. group
  123925. antibiotics
  123926. rohrer
  123927. rokach
  123928. rokhlin
  123929. rokita
  123930. roland
  123931. implications
  123932. anionic
  123933. hydrido
  123934. carbonyl
  123935. protected
  123936. vicinal
  123937. controller
  123938. intramolecula
  123939. alkali
  123940. halides
  123941. synthesis
  123942. nitrogen
  123943. containi
  123944. chiral
  123945. auxiliaries
  123946. intramolecular
  123947. diels
  123948. protic
  123949. dipolar
  123950. aprotic
  123951. solvents
  123952. heterocyclic
  123953. pseudorotation
  123954. stereochemistry
  123955. nucleophili
  123956. quinone
  123957. methide
  123958. sequence
  123959. specific
  123960. alkylation
  123961. iodide
  123962. sequence-selective
  123963. cleavage
  123964. electrochemical
  123965. method
  123966. transformation
  123967. vicinal
  123968. controller
  123969. discriminating
  123970. roles
  123971. rolla
  123972. roman
  123973. romanchick
  123974. romanchick
  123975. joullie
  123976. triazinoindoles
  123977. romanenko
  123978. romanov
  123979. romeo
  123980. romethyl
  123981. romine
  123982. romney
  123983. daniel
  123984. meyers
  123985. chiral
  123986. racemic
  123987. bicyclic
  123988. lactams
  123989. romuald
  123990. ronald
  123991. rondesvedt
  123992. ronec
  123993. rongqin
  123994. rongsi
  123995. practical
  123996. guide
  123997. maintenance
  123998. roof-shaped
  123999. temperature
  124000. stable
  124001. lithiothiophene
  124002. facile
  124003. synthesis
  124004. bjoern
  124005. serrano
  124006. andres
  124007. merchan
  124008. manuela
  124009. multiconfi
  124010. roper
  124011. ropes
  124012. rosaria
  124013. rosemary
  124014. rosen
  124015. rosen
  124016. terry
  124017. nagel
  124018. arthur
  124019. rizzi
  124020. james
  124021. novel
  124022. serotonin
  124023. rosenblatt
  124024. rosenblum
  124025. rosenfarb
  124026. rosenfeld
  124027. rosenmund
  124028. rosenthal
  124029. roser
  124030. roseus
  124031. rosini
  124032. rosini
  124033. carlo
  124034. franzini
  124035. livia
  124036. raffaelli
  124037. andrea
  124038. salvadori
  124039. piero
  124040. rosmarinecine
  124041. rosowsky
  124042. rossa
  124043. rossi
  124044. rossi
  124045. insect
  124046. pheromones
  124047. synthesis
  124048. chiral
  124049. components
  124050. rossiter
  124051. rossiter
  124052. bryante
  124053. swingle
  124054. nicole
  124055. asymmetric
  124056. conjugate
  124057. addit
  124058. rostovshchikova
  124059. rotation
  124060. rotational
  124061. rotational
  124062. isomerism
  124063. trans-12-diarylethyl
  124064. rotations
  124065. rotaxanes
  124066. rotenoids
  124067. rotenoids
  124068. their
  124069. biosynthesis
  124070. heinz
  124071. structure
  124072. reactivity
  124073. organic
  124074. radical
  124075. rothe
  124076. rotstein
  124077. rouessac
  124078. rougier
  124079. rouillard
  124080. roundhill
  124081. roundhill
  124082. transition
  124083. metal
  124084. enzyme
  124085. catalyzed
  124086. reacti
  124087. roush
  124088. roussel
  124089. roussel
  124090. christian
  124091. piras
  124092. patrick
  124093. chirbase
  124094. molecular
  124095. databas
  124096. route
  124097. route
  124098. routes
  124099. aromatic
  124100. polycarbonates
  124101. special
  124102. material
  124103. rouvier
  124104. rowley
  124105. rowley
  124106. deoxygenation
  124107. using
  124108. phosphorus
  124109. reagents
  124110. roxaticin
  124111. roxburgh
  124112. roxburgh
  124113. craig
  124114. syntheses
  124115. medium
  124116. sized
  124117. rings
  124118. royal
  124119. royer
  124120. royer
  124121. enzyme
  124122. synthetic
  124123. catalysts
  124124. synzymes
  124125. rozanne
  124126. rozanov
  124127. rozema
  124128. rozen
  124129. rozovskii
  124130. rozwadowska
  124131. route
  124132. routes@
  124133. ruane@
  124134. rudolf
  124135. russell
  124136. russian
  124137. ruthenium
  124138. osmium
  124139. complexes
  124140. containing
  124141. cyclopentadienyl
  124142. gronowitz
  124143. scripta
  124144. nobel
  124145. symposium
  124146. asymmetric
  124147. weinreb
  124148. alkaloid
  124149. total
  124150. synthesis@
  124151. ranganathan
  124152. panda
  124153. fascinating
  124154. problems
  124155. organic
  124156. zehani
  124157. gelbard
  124158. reductions
  124159. sadovnikova
  124160. belikov
  124161. industrial
  124162. applications
  124163. amino@
  124164. sakamoto
  124165. yamanaka
  124166. conversion
  124167. simple
  124168. pyrimidines
  124169. salts
  124170. samarium
  124171. sammes
  124172. santaniello@
  124173. sarel
  124174. saturated
  124175. unsaturated
  124176. hydrocarbons@
  124177. sawada
  124178. hideo
  124179. synthesis
  124180. perfluoro
  124181. alkylated
  124182. compounds
  124183. scandium
  124184. trifluoromethanesulf
  124185. novel
  124186. catalyst
  124187. friedel
  124188. schaffner
  124189. schiemann@
  124190. schmidt
  124191. bromotrimethylsilane
  124192. iodotrimethylsilane
  124193. rs-functions
  124194. 12-catalyzed
  124195. coupling
  124196. hetroaromatic
  124197. c-h/co/olefins
  124198. shahrokh
  124199. solvation
  124200. rubber
  124201. rubezhov
  124202. rubin
  124203. rubinovitz
  124204. rubio
  124205. rubiralta
  124206. rubiralta
  124207. mario
  124208. giralt
  124209. ernest
  124210. piperidine
  124211. structure
  124212. rubottom
  124213. rubrolone
  124214. ruccia
  124215. ruccia
  124216. vivona
  124217. spinelli
  124218. mononuclear
  124219. heterocyclic
  124220. rearra
  124221. ruchardt
  124222. ruchardt
  124223. beckhaus
  124224. towards
  124225. understanding
  124226. ruchardt
  124227. steric
  124228. effects
  124229. radical
  124230. chemistry
  124231. ruchardt
  124232. christoph
  124233. meier
  124234. michael
  124235. klaus
  124236. pakusch
  124237. joachim
  124238. ruchirawat
  124239. rucl2
  124240. ruclh
  124241. ructure
  124242. rudakov
  124243. rudchenko
  124244. rudchenko
  124245. vladimir
  124246. synthesis
  124247. reactions
  124248. properties
  124249. rudiger
  124250. rudler
  124251. rudler
  124252. audouin
  124253. chelain
  124254. denise
  124255. goumont
  124256. aminocarbene
  124257. rudnev
  124258. rudolf
  124259. rudolf
  124260. rudolph
  124261. rudorf
  124262. rudorf
  124263. dieter
  124264. reactions
  124265. carbon
  124266. disulfide
  124267. ruediger
  124268. organic
  124269. reactions
  124270. equilibria
  124271. kinetics
  124272. mechanism
  124273. ruffing
  124274. ruffolo
  124275. ruffolo
  124276. robert
  124277. chirality
  124278. alpha
  124279. adrenoceptor
  124280. ruggero
  124281. rugulovasines
  124282. ruleI
  124283. rules
  124284. rulin
  124285. rumin
  124286. runge
  124287. runge
  124288. substituent
  124289. effects
  124290. allenes
  124291. cumulenes
  124292. ruo4v
  124293. ruppert
  124294. ruppin
  124295. rus-common
  124296. rusanov
  124297. rusch
  124298. rusinov
  124299. rusling
  124300. russell
  124301. russell
  124302. russell
  124303. molecular
  124304. conformational
  124305. equilibria
  124306. studied
  124307. russian
  124308. russian
  124309. russian
  124310. rutamycin
  124311. ruthenium
  124312. mplexes
  124313. containing
  124314. cyclopentadienyl
  124315. ruthenium
  124316. catalyzed
  124317. addition
  124318. allyl
  124319. alcohols
  124320. acetylene
  124321. ruthenium
  124322. catalyzed
  124323. enyne
  124324. metathesis
  124325. ruthenium
  124326. catalyzed
  124327. oxidative
  124328. transformations
  124329. alcohols
  124330. ruthenium
  124331. complexes
  124332. organic
  124333. oxidants
  124334. ruthenium-catalyzed
  124335. ruthenium-catalyzed
  124336. oxidative
  124337. transformations
  124338. alcohols
  124339. ruthenium-catalyzed
  124340. reaction
  124341. 16-diynes
  124342. hydrosilanes
  124343. ruthenocenylbis
  124344. rutledge
  124345. ruveda
  124346. ruzicka
  124347. ryabov
  124348. ryabov
  124349. alexander
  124350. biochemical
  124351. reactions
  124352. organometall
  124353. ryakhovskii
  124354. ryakhovskii
  124355. agafonov
  124356. kosyrev
  124357. special
  124358. features
  124359. ryanodine
  124360. ryashentseva
  124361. ryashentseva
  124362. maragarita
  124363. catalytic
  124364. synthesis
  124365. thiophene
  124366. rybakova
  124367. rybakova
  124368. prilezhaeva
  124369. litvinov
  124370. methods
  124371. replaci
  124372. rybin
  124373. rybinskaya
  124374. rychly
  124375. rychnovsky
  124376. rydberg
  124377. rylander
  124378. rylander
  124379. catalytic
  124380. hydrogenation
  124381. organic
  124382. syntheses
  124383. ryoichi
  124384. ryoji
  124385. ryszard
  124386. rytina
  124387. rytting
  124388. rzaev
  124389. rzeszotarska
  124390. maslov
  124391. blyumberg
  124392. liqui
  124393. braslavsky
  124394. heicklen
  124395. phase
  124396. thermal
  124397. photoc
  124398. braverman
  124399. chemistry
  124400. allenes
  124401. weizmann
  124402. press
  124403. jerusalem
  124404. colonna
  124405. banfi
  124406. papagni
  124407. venkataramu
  124408. macdonell
  124409. purdum
  124410. david
  124411. hanessian
  124412. tetrahedron
  124413. regioselecti
  124414. zurabyan
  124415. khorlin
  124416. advan
  124417. isoquinoline
  124418. alkaloid
  124419. biosynthesis
  124420. speculations
  124421. mason
  124422. foundations
  124423. classical
  124424. stereochemistry
  124425. davies
  124426. london
  124427. asymmetric
  124428. synthesis
  124429. gronowitz
  124430. scripta
  124431. nobel
  124432. symposium
  124433. asymmetric
  124434. unger
  124435. hansch
  124436. quantitative
  124437. models
  124438. steric
  124439. effects
  124440. hanessian
  124441. rancourt
  124442. approaches
  124443. total
  124444. synthesis
  124445. hibino
  124446. synthetic
  124447. approaches
  124448. streptonigrin
  124449. biologica
  124450. hoare
  124451. synthetic
  124452. peptides
  124453. millig
  124454. indacene
  124455. delocalized
  124456. formally
  124457. antiaromatic
  124458. electron
  124459. danishefsky
  124460. aldrichimica
  124461. evolution
  124462. wilen
  124463. collet
  124464. jacques
  124465. strategies
  124466. optical
  124467. resol
  124468. pradhan
  124469. tetrahedron
  124470. mechanism
  124471. stereoche
  124472. murai
  124473. ishida
  124474. proced
  124475. schreiber
  124476. science
  124477. photocycloadditions
  124478. robert
  124479. bicyclo
  124480. 3.2.0
  124481. heptanones
  124482. hecht
  124483. isomeric
  124484. trna's
  124485. protein
  124486. biosynthesis
  124487. hecht
  124488. utilization
  124489. isomeric
  124490. aminoacyl
  124491. transfer
  124492. ribonuc
  124493. makin
  124494. ether
  124495. weinreb
  124496. alkaloid
  124497. total
  124498. synthesis
  124499. weinreb
  124500. semmelhack
  124501. accounts
  124502. masamune
  124503. angew
  124504. double
  124505. masamune
  124506. bates
  124507. corcoran
  124508. macrolide
  124509. chemistry
  124510. masamune
  124511. petersen
  124512. angew
  124513. mickel
  124514. aldrichimica
  124515. acetoxy
  124516. azetidinon
  124517. misumi
  124518. symposium
  124519. lecture
  124520. cyclo
  124521. nakamura
  124522. kondo
  124523. brief
  124524. review
  124525. nucleoside
  124526. antibiot
  124527. ogino
  124528. rearrangements
  124529. amine
  124530. oxides
  124531. furukawa
  124532. reactions
  124533. sulfilimines
  124534. kunieda
  124535. sulfinic
  124536. acids
  124537. sulfinic
  124538. esters
  124539. organ
  124540. sulfoxides
  124541. sulfilimines
  124542. organic
  124543. chemistry
  124544. sulfu
  124545. fukushima
  124546. takata
  124547. oxidation
  124548. biologic
  124549. interaction
  124550. controlling
  124551. factor
  124552. stereoselecti
  124553. rajappa
  124554. synthesis
  124555. heterocycles
  124556. enamines
  124557. ranganathan
  124558. panda
  124559. fascinating
  124560. problems
  124561. organic
  124562. ranganathan
  124563. ranganathan
  124564. mehrotra
  124565. ketene
  124566. equivale
  124567. rozen
  124568. filler
  124569. tetrahedron
  124570. alpha
  124571. fluoroca
  124572. silylmethyl
  124573. substituted
  124574. ketene
  124575. dithioacetals
  124576. synthetic
  124577. sivaram
  124578. dimerization
  124579. ethylen
  124580. skonieczny
  124581. synthesis
  124582. substituted
  124583. acridines
  124584. purrington
  124585. kagen
  124586. patrick
  124587. kalista
  124588. listy
  124589. utilization
  124590. torii
  124591. electroorganic
  124592. synthesis
  124593. methods
  124594. applications
  124595. torii
  124596. synthesis
  124597. electroreductive
  124598. turner
  124599. principles
  124600. synthetic
  124601. desig
  124602. london
  124603. organoselenium
  124604. mediated
  124605. staley
  124606. pericyclic
  124607. reactions
  124608. carbanions
  124609. pericyclic
  124610. washburne
  124611. organomet
  124612. silicon
  124613. application
  124614. london
  124615. synthetic
  124616. applications
  124617. zehani
  124618. gelbard
  124619. reductions
  124620. s-bond
  124621. s-cis
  124622. s-ester
  124623. s-esters
  124624. s-nucleophiles
  124625. s-oxidation
  124626. s-palladium
  124627. s-trans
  124628. s/n-acetals
  124629. s/s-acetals
  124630. saavedra
  124631. sabastiao
  124632. saberi
  124633. sabina
  124634. sabine
  124635. saccharide
  124636. saccharides
  124637. saccharides
  124638. biological
  124639. importance
  124640. challenges
  124641. opportun
  124642. saccharinic
  124643. sachihiko
  124644. sachs
  124645. sachtler
  124646. sacrificial
  124647. sadducts
  124648. sadek
  124649. sadekov
  124650. sadekov
  124651. minkin
  124652. semenov
  124653. shevelev
  124654. doubly
  124655. stabi
  124656. sadekov
  124657. bushkov
  124658. minkin
  124659. synthesis
  124660. struct
  124661. sadekov
  124662. minkin
  124663. vladimir
  124664. tellurium
  124665. containing
  124666. hetero
  124667. sadova
  124668. sadova
  124669. khaikin
  124670. vilkov
  124671. problems
  124672. stere
  124673. sadovnikova
  124674. sadovnikova
  124675. belikov
  124676. industrial
  124677. applications
  124678. amino
  124679. sadowski
  124680. sadowski
  124681. gasteiger
  124682. johann
  124683. atoms
  124684. bonds
  124685. three
  124686. sadykov
  124687. saegusa
  124688. saenger
  124689. saenger
  124690. niemann
  124691. herbst
  124692. hinrichs
  124693. steiner
  124694. crystal
  124695. saeva
  124696. safener
  124697. safety
  124698. safety
  124699. precautions
  124700. organic
  124701. peroxy
  124702. compounds
  124703. safracins
  124704. saframycins
  124705. saginaev
  124706. sagitullin
  124707. sahakitpichan
  124708. saini
  124709. sainsburyW
  124710. sainsbury
  124711. modern
  124712. methods
  124713. formation
  124714. sainsbury
  124715. polycyclic
  124716. compounds
  124717. fused
  124718. condensed
  124719. cyclic
  124720. saito
  124721. saito
  124722. matsuura
  124723. oxidations
  124724. electron
  124725. aromatic
  124726. saito
  124727. absolute
  124728. stereochemistry
  124729. chelate
  124730. complexes
  124731. sajdl
  124732. sakae
  124733. sakai
  124734. sakakura
  124735. sakamoto
  124736. sakamoto
  124737. yamanaka
  124738. conversion
  124739. simple
  124740. pyrimidines
  124741. sakata
  124742. sakhno
  124743. sakhnrov
  124744. sakuraba
  124745. sakuragi
  124746. sakurai
  124747. sakurai
  124748. hideki
  124749. metamorphosis
  124750. synthetic
  124751. strategies
  124752. salad
  124753. salakhov
  124754. salas
  124755. salaun
  124756. saleh
  124757. salem
  124758. salenG
  124759. salerno
  124760. salicylic
  124761. salicylidenamino
  124762. salomon
  124763. salomon
  124764. claudio
  124765. ernesto
  124766. recent
  124767. developments
  124768. chemic
  124769. saloutin
  124770. effects
  124771. organic
  124772. organometallic
  124773. chemistry
  124774. salter
  124775. saltiel
  124776. saltiel
  124777. charlton
  124778. trans
  124779. isomerization
  124780. olefins
  124781. salts
  124782. salts
  124783. salts/ions
  124784. salvadori
  124785. salvadori
  124786. piero
  124787. bertucci
  124788. carlo
  124789. rosini
  124790. carlo
  124791. circular
  124792. dichroi
  124793. salvadori
  124794. piero
  124795. dario
  124796. rosini
  124797. carlo
  124798. bertucci
  124799. carlo
  124800. uccel
  124801. salvage
  124802. salvilenone
  124803. salzbrenner
  124804. salzer
  124805. samadi
  124806. samankumara
  124807. samarai
  124808. samarium
  124809. samarium
  124810. ytterbium
  124811. reagents
  124812. samarium
  124813. diiodide
  124814. induced
  124815. reduction
  124816. amorphous
  124817. selenium
  124818. samarium
  124819. diiodide
  124820. mediated
  124821. deoxygenation
  124822. taxol
  124823. samarium
  124824. iodide
  124825. organie
  124826. synthesis
  124827. samarium
  124828. iodide
  124829. induced
  124830. radical
  124831. cyclization
  124832. samarium
  124833. iodide
  124834. induced
  124835. radical
  124836. cyclizations
  124837. samarium
  124838. iodide
  124839. mediated
  124840. intermolecular
  124841. ketone-oefin
  124842. samarium
  124843. iodide
  124844. promoted
  124845. contraction
  124846. carbohydrate
  124847. samarium
  124848. iodide
  124849. preparation
  124850. reactions
  124851. samarium
  124852. iodide
  124853. induced
  124854. intramolecular
  124855. glycoside
  124856. formation
  124857. samarium
  124858. iodide
  124859. reductive
  124860. addition
  124861. phenylsulfones
  124862. sambasivarao
  124863. sambucinol
  124864. sammes
  124865. sammes
  124866. sammes
  124867. yahioglu
  124868. phenanthroline
  124869. versatile
  124870. ligand
  124871. samodurova
  124872. sample
  124873. samuel
  124874. samuelsson
  124875. samuilov
  124876. sanchez
  124877. sanchez
  124878. ribot
  124879. design
  124880. hybrid
  124881. organic
  124882. inorganic
  124883. materia
  124884. sandanayake
  124885. sande
  124886. sander
  124887. sander
  124888. wolfram
  124889. bucher
  124890. goetz
  124891. wierlacher
  124892. stefan
  124893. carbenes
  124894. sanders
  124895. sanders
  124896. spectral
  124897. change
  124898. probe
  124899. chlorophyll
  124900. sandhu
  124901. sandler
  124902. sandler
  124903. stanley
  124904. sourcebook
  124905. advanced
  124906. organic
  124907. sandorfy
  124908. sandorfy
  124909. ultraviolet
  124910. absorption
  124911. spectra
  124912. organic
  124913. sandri
  124914. sandrini
  124915. sandro
  124916. sandstrom
  124917. sandwich
  124918. sandwiches
  124919. sanfilippo
  124920. sanford
  124921. sangwan
  124922. sanien
  124923. sanner
  124924. sannigrabi
  124925. sansone
  124926. santaniello
  124927. santaniello
  124928. ferraboschi
  124929. patrizia
  124930. grisenti
  124931. paride
  124932. manzoc
  124933. santavy
  124934. santavy
  124935. alkaloids
  124936. plants
  124937. subfamily
  124938. wurmbaeoide
  124939. santavy
  124940. papaveraceae
  124941. alkaloids
  124942. alkaloids
  124943. santelli
  124944. santhanakrishnan
  124945. santos
  124946. santoyo
  124947. santoyo
  124948. gonzalez
  124949. francisco
  124950. hernandez
  124951. mateo
  124952. fernando
  124953. synthesi
  124954. santry
  124955. santus
  124956. santus
  124957. bazin
  124958. aubailly
  124959. nature
  124960. identification
  124961. proper
  124962. saobah
  124963. saoud
  124964. sapogeninsX
  124965. saponin
  124966. saponinsX
  124967. sappa
  124968. sapphyrins
  124969. sapphyrins
  124970. expanded
  124971. porphyrin
  124972. sapphyrns
  124973. saraf
  124974. saraf
  124975. proton
  124976. magnetic
  124977. resonance
  124978. spectra
  124979. acridizinium
  124980. saraf
  124981. absorption
  124982. spectra
  124983. benzologs
  124984. quinolizinium
  124985. saraf
  124986. chemistry
  124987. benzo
  124988. benzo
  124989. quinoli
  124990. sarah
  124991. sarain
  124992. sarcocapnine
  124993. sarel
  124994. sarel
  124995. sarel
  124996. metal
  124997. induced
  124998. rearrangements
  124999. insertions
  125000. sargent
  125001. sargeson
  125002. sarkar
  125003. sarlo
  125004. sarma
  125005. sarpagin
  125006. sarybaeva
  125007. sarybaeva
  125008. afanas'ev
  125009. zaikov
  125010. shchelokhova
  125011. sasaki
  125012. sasaki
  125013. typed
  125014. heterocyclic
  125015. compounds
  125016. hetero
  125017. sason
  125018. sastry
  125019. satchell
  125020. satge
  125021. sativa
  125022. sativene
  125023. fumie
  125024. kobayashi
  125025. yuichi
  125026. synthesis
  125027. enantiomerically
  125028. satoh
  125029. satoh
  125030. tsuyoshi
  125031. yamakawa
  125032. organic
  125033. synthesis
  125034. sulfinyl
  125035. satoh
  125036. tsuyoshi
  125037. yamakawa
  125038. recent
  125039. developments
  125040. organic
  125041. satoru
  125042. satoshi
  125043. sattanasin
  125044. sattur
  125045. saturated
  125046. saturated
  125047. unsaturated
  125048. hydrocarbons
  125049. saturated
  125050. bicyclic
  125051. ring-fused
  125052. systems
  125053. bridgehead
  125054. saturated
  125055. carbon-hydrogen
  125056. activation
  125057. saturated
  125058. nitrogen
  125059. heterocycles
  125060. saturated
  125061. oxygen
  125062. heterocycles
  125063. satyavan
  125064. sauer
  125065. sauer
  125066. sustmann
  125067. mechanistic
  125068. aspects
  125069. diels
  125070. alder
  125071. reacti
  125072. saulnier
  125073. saumitra
  125074. saunders
  125075. saunders
  125076. chandrasekhar
  125077. schleyer
  125078. rearrangements
  125079. saunders
  125080. martin
  125081. jimenez
  125082. vazquez
  125083. recent
  125084. studies
  125085. sauvage
  125086. sauvage
  125087. dietrich
  125088. buchecker
  125089. interlocked
  125090. knotted
  125091. savage
  125092. savard
  125093. saveantq
  125094. saveant
  125095. mechanisms
  125096. reactivity
  125097. electron
  125098. transfer
  125099. savin
  125100. savinykh
  125101. savona
  125102. sawada
  125103. sawada
  125104. hideo
  125105. fluorinated
  125106. organic
  125107. peroxides
  125108. their
  125109. decompositi
  125110. sawada
  125111. hideo
  125112. synthesis
  125113. perfluoro
  125114. alkylated
  125115. compounds
  125116. sawamura
  125117. sawamura
  125118. masaya
  125119. yoshihiko
  125120. catalytic
  125121. asymmetric
  125122. synthesis
  125123. sawflies
  125124. saxena
  125125. saxena
  125126. hosmane
  125127. narayan
  125128. recent
  125129. advances
  125130. chemi
  125131. saxitoxin
  125132. saxton
  125133. saxton
  125134. recent
  125135. progress
  125136. chemistry
  125137. indole
  125138. alkalo
  125139. sayakhov
  125140. sbraletta
  125141. scaiano
  125142. scaiano
  125143. lissi
  125144. encina
  125145. chemistry
  125146. biradicals
  125147. scale
  125148. scalemic
  125149. scales
  125150. scales
  125151. nucleophilicity
  125152. electrophilicity
  125153. system
  125154. scaling
  125155. scalsno
  125156. scand
  125157. scandinavica
  125158. scandium
  125159. scandium
  125160. perchlorate
  125161. novel
  125162. catalyst
  125163. scandium
  125164. trifluoromethanesulf
  125165. novel
  125166. catalyst
  125167. friedel
  125168. scandola
  125169. scandola
  125170. photochemical
  125171. rearrangements
  125172. coordination
  125173. scanlon
  125174. scanlon
  125175. thomas
  125176. schulz
  125177. peter
  125178. recent
  125179. advances
  125180. catalytic
  125181. scartazzini
  125182. scartazzini
  125183. bickel
  125184. orally
  125185. active
  125186. cephalosporins
  125187. scavenging
  125188. scavenging
  125189. hydrated
  125190. electrons
  125191. hydrophobic
  125192. solutes
  125193. sceletium
  125194. scent
  125195. scettri
  125196. schaap
  125197. schaap
  125198. zaklika
  125199. cycloaddition
  125200. reactions
  125201. singlet
  125202. schacht
  125203. schack
  125204. schack
  125205. christe
  125206. reactions
  125207. electropositive
  125208. chlorine
  125209. schaefer
  125210. schaefer
  125211. hydrogen
  125212. shift
  125213. common
  125214. vehicle
  125215. schaefer
  125216. stejskal
  125217. resolution
  125218. solid
  125219. schafer
  125220. schafer
  125221. andrea
  125222. herbert
  125223. fiedler
  125224. wolfgang
  125225. guggisberg
  125226. schafer
  125227. anodic
  125228. cathodic
  125229. formation
  125230. schaffner
  125231. schaffner
  125232. schaffner
  125233. demuth
  125234. photochemical
  125235. rearrangements
  125236. conjuga
  125237. schaller
  125238. schamp
  125239. scharf
  125240. scharf
  125241. frauenrach
  125242. mycotoxin
  125243. moniliformin
  125244. relat
  125245. schaumann
  125246. schaverien
  125247. schaverien
  125248. colin
  125249. organometallic
  125250. chemistry
  125251. lanthanid
  125252. scheeren
  125253. scheffer
  125254. scheffold
  125255. scheffold
  125256. modern
  125257. synthetic
  125258. methods
  125259. verlag
  125260. scheinmann
  125261. scheithauer
  125262. scheithauer
  125263. mayer
  125264. dithiocarbolcylic
  125265. acids
  125266. schell
  125267. schellenberger
  125268. schellenberger
  125269. volker
  125270. jakubke
  125271. dieter
  125272. protease
  125273. catalyzed
  125274. schemes
  125275. schenck
  125276. schenk
  125277. schenkluhn
  125278. scherer
  125279. scheuer
  125280. scheuer
  125281. varied
  125282. fascinating
  125283. chemistry
  125284. marine
  125285. scheunemann
  125286. schick
  125287. schiemann
  125288. schiff
  125289. schildknecht
  125290. schildknecht
  125291. irritant
  125292. defense
  125293. substances
  125294. higher
  125295. schindler
  125296. schionato
  125297. schizandrin
  125298. schlegel
  125299. schleicher
  125300. schleyer
  125301. schlogl
  125302. schlosser
  125303. schlosser
  125304. organometallics
  125305. synthesis
  125306. wiley
  125307. chichester
  125308. schlosser
  125309. introduction
  125310. fluorine
  125311. organic
  125312. molecules
  125313. schlosser
  125314. manfred
  125315. desponds
  125316. olivier
  125317. lehmann
  125318. moret
  125319. etienn
  125320. schlunegger
  125321. schlunegger
  125322. advanced
  125323. spectrometry
  125324. applications
  125325. schmalz
  125326. schmalz
  125327. gunther
  125328. chromium
  125329. carbene
  125330. complexes
  125331. organic
  125332. schmehl
  125333. schmeltz
  125334. schmid
  125335. schmidbaur
  125336. schmidbaur
  125337. hubert
  125338. concepts
  125339. chemistry
  125340. schmidt
  125341. schmidt
  125342. bromotrimethylsilane
  125343. iodotrimethylsilane
  125344. schmidt
  125345. reactions
  125346. squaric
  125347. derivatives
  125348. schmidt
  125349. preparative
  125350. chemistry
  125351. cyclobutendi
  125352. schmidt
  125353. synthesis
  125354. cyclobutenedione
  125355. schmidt
  125356. chemistry
  125357. squaraines
  125358. oxocarbons
  125359. schmidt
  125360. bifunctional
  125361. thioethers
  125362. complex
  125363. ligands
  125364. schmidt
  125365. hausler
  125366. ohler
  125367. poisel
  125368. dehydroamino
  125369. acids
  125370. schmit
  125371. schmittel
  125372. schmittel
  125373. michael
  125374. umpolung
  125375. ketones
  125376. radical
  125377. catio
  125378. schmittgen
  125379. schmitz
  125380. schmitz
  125381. three
  125382. membered
  125383. rings
  125384. heteroatoms
  125385. schmuck
  125386. schnapp
  125387. schnatter
  125388. schneider
  125389. schneider
  125390. histidine
  125391. enzyme
  125392. active
  125393. centers
  125394. schneider
  125395. linear
  125396. energy
  125397. relationships
  125398. pairwise
  125399. schneider
  125400. joerg
  125401. supramolecular
  125402. chemistry
  125403. spectro
  125404. schneider
  125405. frontiers
  125406. supramolecular
  125407. organic
  125408. schneider
  125409. mechanisms
  125410. molecular
  125411. recognition
  125412. schneller
  125413. schnoes
  125414. schock
  125415. schoemaker
  125416. schoemaker
  125417. chemistry
  125418. lignin
  125419. biodegradation
  125420. schoemaker
  125421. chemistry
  125422. lignin
  125423. biodegradation
  125424. schoffstall
  125425. schollkopf
  125426. schomburg
  125427. schomburg
  125428. chromatography
  125429. practical
  125430. course
  125431. weinhe
  125432. schon
  125433. schonberg
  125434. schonberg
  125435. singer
  125436. chemistry
  125437. ninhydrin
  125438. other
  125439. cyclic
  125440. schoofs
  125441. schreiber
  125442. schreiber
  125443. stuart
  125444. albers
  125445. rosen
  125446. michael
  125447. schreiber
  125448. stuart
  125449. verdine
  125450. gregory
  125451. protein
  125452. overproduction
  125453. schripsema
  125454. schriver
  125455. schrock
  125456. schrock
  125457. alkylidene
  125458. complexes
  125459. niobium
  125460. tantalum
  125461. schrock
  125462. recent
  125463. advances
  125464. chemistry
  125465. application
  125466. schroder
  125467. schneider
  125468. frontiers
  125469. supramolecular
  125470. organic
  125471. schroder
  125472. osmium
  125473. tetraoxide
  125474. hydroxylation
  125475. unsaturate@
  125476. schuster
  125477. chemiluminescence
  125478. organic
  125479. peroxides
  125480. science
  125481. scovery@
  125482. secondg
  125483. second-row@
  125484. seevers@
  125485. selective
  125486. selective
  125487. alkylation
  125488. pyridone
  125489. solvent
  125490. condition@
  125491. selective
  125492. catalytic
  125493. oxidative
  125494. cleavage
  125495. oximes
  125496. carbonyl@
  125497. selective
  125498. oxidation
  125499. organometallics
  125500. hydroperoxide@
  125501. selective
  125502. oxygenation
  125503. t-butyl
  125504. hydroperoxide@
  125505. selectivity
  125506. selenium
  125507. tellurium-c
  125508. ntred
  125509. radicals@
  125510. selenosulfonation@
  125511. sellergren@
  125512. seyden
  125513. penne
  125514. jacqueline
  125515. reductions
  125516. alumino
  125517. borohy@
  125518. shapiro@
  125519. sheldon
  125520. shevchenko
  125521. apushkinskii
  125522. quinone
  125523. methides
  125524. chem@
  125525. shigeru
  125526. shinkai
  125527. functionalization
  125528. crown
  125529. ethers
  125530. calixarenes
  125531. shono
  125532. tatsuya
  125533. electroorganic
  125534. synthesis
  125535. academic
  125536. london
  125537. schroder
  125538. osmium
  125539. tetraoxide
  125540. hydroxylation
  125541. unsaturate
  125542. schroth
  125543. schryver
  125544. schubert
  125545. schubert
  125546. ulrich
  125547. formation
  125548. breaking
  125549. review
  125550. schuchardt
  125551. schuchardt
  125552. carvalho
  125553. wagner
  125554. alves
  125555. spinace
  125556. estevam
  125557. vitorio
  125558. schuchmann
  125559. schuda
  125560. schuda
  125561. aflatoxin
  125562. chemistry
  125563. syntheses
  125564. schudde
  125565. schuddeboom
  125566. schuetz
  125567. schug
  125568. schuhert
  125569. schulenberg
  125570. schultz
  125571. schulz
  125572. schumann
  125573. schumann
  125574. herbert
  125575. group
  125576. metallocenes
  125577. substituted
  125578. schurig
  125579. schurig
  125580. volker
  125581. betschinger
  125582. frank
  125583. metal
  125584. mediated
  125585. enantioselec
  125586. schuster
  125587. schuster
  125588. mechanisms
  125589. photochemical
  125590. transformations
  125591. schuster
  125592. photochemical
  125593. rearrangements
  125594. enones
  125595. rearrang
  125596. schuster
  125597. david
  125598. george
  125599. kaprinidis
  125600. nikolas
  125601. insight
  125602. schuster
  125603. chemiluminescence
  125604. organic
  125605. peroxides
  125606. schwab
  125607. schwark
  125608. schwartz
  125609. schwartz
  125610. labinger
  125611. patterns
  125612. organometallic
  125613. chemistry
  125614. schwartz
  125615. laufer
  125616. physical
  125617. chemistry
  125618. aqueo
  125619. schwarz
  125620. schwarz
  125621. pyramidal
  125622. carbocations
  125623. angewandte
  125624. schwarz
  125625. aspects
  125626. spectrometric
  125627. ortho
  125628. effec
  125629. schwarz
  125630. helmut
  125631. mechanism
  125632. fullerene
  125633. formation
  125634. angewand
  125635. schwarzenbach
  125636. schwarzenbach
  125637. gschwend
  125638. philip
  125639. imboden
  125640. dieter
  125641. schwegler
  125642. schweizer
  125643. schwemlein
  125644. schwerdtfeger
  125645. schwertfeger
  125646. schwetlich
  125647. schwetlick
  125648. schwind
  125649. schwind
  125650. gilligan
  125651. gussier
  125652. developing
  125653. commerci
  125654. schwing
  125655. schyja
  125656. scienceQ
  125657. science
  125658. science1994
  125659. sciences
  125660. scientific
  125661. scientist
  125662. scission
  125663. scissor
  125664. scola
  125665. scolastico
  125666. scopadulcic
  125667. scopadulciol
  125668. scope
  125669. scottm
  125670. scott
  125671. biosynthesis
  125672. vitamin
  125673. search
  125674. porph
  125675. scott
  125676. indole
  125677. alkaloid
  125678. biosynthesis
  125679. scott
  125680. nature
  125681. synthesizes
  125682. vitamin
  125683. survey
  125684. scott
  125685. discovery
  125686. nature's
  125687. pathway
  125688. vitamin
  125689. scott
  125690. genetically
  125691. engineered
  125692. synthesis
  125693. complex
  125694. scott
  125695. mechanistic
  125696. aspects
  125697. biosynthesis
  125698. vitam
  125699. scouten
  125700. scovery
  125701. screening
  125702. screttas
  125703. scribner
  125704. scripta
  125705. scriven
  125706. scrowston
  125707. scrowston
  125708. recent
  125709. advances
  125710. chemistry
  125711. benzo
  125712. scudder
  125713. scudder
  125714. electron
  125715. organic
  125716. chemistry
  125717. wiley
  125718. sculpting
  125719. se-se
  125720. seaman
  125721. seaman
  125722. bohlmann
  125723. zdero
  125724. mabry
  125725. diterpenoids
  125726. flower
  125727. search
  125728. search
  125729. configurationally
  125730. stable
  125731. aracemic
  125732. amino
  125733. organol
  125734. searching
  125735. searching
  125736. techniques
  125737. databases
  125738. three
  125739. dimensional
  125740. searle
  125741. seasons
  125742. sebastian
  125743. sebek
  125744. secen
  125745. secies
  125746. seco-acids
  125747. secodine
  125748. secoisoquinoline
  125749. secondW
  125750. secondg
  125751. second-row
  125752. anomeric
  125753. interactions
  125754. involv
  125755. phosphor
  125756. second-sphere
  125757. secondary
  125758. secondary
  125759. orbital
  125760. effects
  125761. fluorine
  125762. compounds
  125763. seconi
  125764. section
  125765. sections
  125766. seddon
  125767. sediments
  125768. seebach
  125769. seebach
  125770. methods
  125771. reactivity
  125772. umpolung
  125773. 197918
  125774. angewand
  125775. seebach
  125776. dieter
  125777. stumbled
  125778. peptide
  125779. chemistry
  125780. seeger
  125781. christian
  125782. vogtle
  125783. fritz
  125784. molecules
  125785. large
  125786. cavities
  125787. seeman
  125788. seemayer
  125789. seetha
  125790. seevers
  125791. segal
  125792. segment
  125793. segments
  125794. seguin
  125795. sehuchmann
  125796. seibl
  125797. seige
  125798. seiichiro
  125799. seiji
  125800. seikaly
  125801. seitembetova
  125802. seitz
  125803. seitz
  125804. thioxocarbon
  125805. dianions
  125806. their
  125807. derivatives
  125808. oxocar
  125809. seitz
  125810. gunther
  125811. imming
  125812. peter
  125813. oxocarbons
  125814. pseudooxocarbons
  125815. selected
  125816. selected
  125817. applications
  125818. organic
  125819. synthesis
  125820. intramolecular
  125821. selected
  125822. methods
  125823. oxidation
  125824. carbohydrate
  125825. chemistry
  125826. selected
  125827. topics
  125828. wittig
  125829. reaction
  125830. synthesis
  125831. selected
  125832. transformations
  125833. cyclopropylidene
  125834. oxaspiro
  125835. selectin
  125836. selectins
  125837. selection
  125838. selective
  125839. selective
  125840. pyridone
  125841. solvent
  125842. condition
  125843. selective
  125844. anodic
  125845. partial
  125846. fluorination
  125847. heteroatom
  125848. compound
  125849. selective
  125850. biocatalysis
  125851. synthetic
  125852. approach
  125853. selective
  125854. formation
  125855. based
  125856. organosilicon
  125857. reagents
  125858. selective
  125859. carbanion
  125860. chemistry
  125861. anion-cation
  125862. interactions
  125863. selective
  125864. catalytic
  125865. oxidative
  125866. cleavage
  125867. oximes
  125868. carbonyl
  125869. selective
  125870. cleavage
  125871. alkyl
  125872. ethers
  125873. thioethers
  125874. selen
  125875. selective
  125876. demethylation
  125877. demethoxy
  125878. thioalkylation
  125879. selective
  125880. deoxygenation
  125881. allylic
  125882. alcohols
  125883. acetates
  125884. selective
  125885. deprotection
  125886. allyl
  125887. amines
  125888. using
  125889. palladium
  125890. selective
  125891. electrophilic
  125892. activation
  125893. alkanes
  125894. selective
  125895. formation
  125896. propargylsilanes
  125897. allenylsilanes
  125898. selective
  125899. functionalization
  125900. conformational
  125901. properties
  125902. selective
  125903. generation
  125904. radicals
  125905. epoxides
  125906. using
  125907. selective
  125908. hydrogenation
  125909. simple
  125910. functionalized
  125911. conjuga
  125912. selective
  125913. hydrogenation
  125914. unsaturated
  125915. ketones
  125916. acetylene
  125917. selective
  125918. lithiation
  125919. bromoarylalkanoic
  125920. acids
  125921. amides
  125922. selective
  125923. methylation
  125924. arylacetonitriles
  125925. methyl
  125926. selective
  125927. oxidation
  125928. alpha
  125929. beta-unsaturated
  125930. ketones
  125931. selective
  125932. oxidations
  125933. peroxid
  125934. based
  125935. reagents
  125936. selective
  125937. oxygenation
  125938. t-butyl
  125939. hydroperoxide
  125940. selective
  125941. reactions
  125942. using
  125943. allyli
  125944. metals
  125945. selective
  125946. reactions
  125947. organoaluminium
  125948. compounds
  125949. selective
  125950. reductions
  125951. simple
  125952. technique
  125953. achieve
  125954. selective
  125955. removal
  125956. protecting
  125957. group
  125958. presen
  125959. selective
  125960. removal
  125961. protecting
  125962. group
  125963. prese
  125964. selective
  125965. replacement
  125966. hydrogen
  125967. saturated
  125968. carbon
  125969. selective
  125970. ring-opening
  125971. cross
  125972. metathesis
  125973. short
  125974. synthesis
  125975. selective
  125976. synthesis
  125977. lewis
  125978. acids
  125979. presence
  125980. selective
  125981. synthesis
  125982. aromatic
  125983. compounds
  125984. using
  125985. positional
  125986. selectively
  125987. selectivities
  125988. selectivities
  125989. palladium
  125990. catalyzed
  125991. synthesis
  125992. dimeth
  125993. selectivity
  125994. selectivity
  125995. selectivity
  125996. mechanism
  125997. catalytical
  125998. asymmetric
  125999. synthesi
  126000. selectivity
  126001. synthetic
  126002. applications
  126003. radical
  126004. reactions
  126005. selectivity
  126006. palladium
  126007. catalyzed
  126008. allylic
  126009. substitution
  126010. selena
  126011. selenadiazoles
  126012. selenenylating
  126013. selenide
  126014. selenides
  126015. selenium
  126016. selenium
  126017. tellurium
  126018. centered
  126019. radicals
  126020. selenium
  126021. tellurium
  126022. reagents
  126023. preparation
  126024. thetic
  126025. selenium
  126026. tellurium-c
  126027. ntred
  126028. radicals
  126029. selenium
  126030. dioxide
  126031. oxidation
  126032. selenium
  126033. dioxide
  126034. oxidation
  126035. norman
  126036. rabjohn
  126037. organic
  126038. reactions
  126039. selenium
  126040. natural
  126041. product
  126042. synthesis
  126043. selenium
  126044. induced
  126045. stereoselective
  126046. cyclization
  126047. substitute
  126048. selenium
  126049. reagents
  126050. intermediates
  126051. organic
  126052. synthesis
  126053. selenium
  126054. reagents
  126055. organic
  126056. synthesis
  126057. selenium
  126058. stabilization
  126059. selenium-assisted
  126060. selenium-assisted
  126061. carbonylation
  126062. carbon
  126063. monoxide
  126064. selenium-containing
  126065. selenium-nitrogen
  126066. selenium-stabilized
  126067. selenium-stabilized
  126068. carbanions
  126069. seleno
  126070. seleno-2-silylethene
  126071. seleno-sugar
  126072. selenocyclopropanes
  126073. selenoesters
  126074. selenoesters
  126075. oxidation
  126076. states
  126077. selenoethers
  126078. selenoglycopyranoses
  126079. selenolate
  126080. selenolesters
  126081. selenomalonitriles
  126082. selenones
  126083. selenophenes
  126084. selenophenes
  126085. tellurophenes
  126086. their
  126087. benzo
  126088. derivatives
  126089. selenopyrans
  126090. selenosulfonation
  126091. selenoxide
  126092. assembly
  126093. macromolecular
  126094. design
  126095. condensation
  126096. arylthioacetamides
  126097. novel
  126098. syntheses
  126099. self-assembly
  126100. self-assembly
  126101. organic
  126102. synthesis
  126103. self-assembly
  126104. fullerenes
  126105. self-organization
  126106. self-recognition
  126107. selvaraj
  126108. semenov
  126109. semesters
  126110. semiconductor
  126111. semiconductors
  126112. semicorrins
  126113. semicyclic
  126114. semiempirical
  126115. semihydrogenation
  126116. semikolenov
  126117. semikolenov
  126118. modern
  126119. approaches
  126120. preparation
  126121. seminar
  126122. semiochemicals
  126123. semioxocarbons
  126124. semipinacol
  126125. semmelhack
  126126. semple
  126127. semple
  126128. joullie
  126129. synthesis
  126130. reduced
  126131. furans
  126132. senanni
  126133. sener
  126134. sener
  126135. recent
  126136. results
  126137. search
  126138. bioactive
  126139. compounds
  126140. sener
  126141. recent
  126142. results
  126143. search
  126144. bioactive
  126145. compounds
  126146. senga
  126147. sengupta
  126148. seniz
  126149. senning
  126150. sense
  126151. sensitised
  126152. sensitised
  126153. photooxygenation
  126154. olefins
  126155. sensitive
  126156. sensitized
  126157. sensitized
  126158. photooxygenation
  126159. olefins
  126160. denny
  126161. nicko
  126162. sensor
  126163. sensors
  126164. seoane
  126165. seoane
  126166. quinteiro
  126167. synthetic
  126168. approaches
  126169. separate_
  126170. separated
  126171. separation
  126172. separations
  126173. sepnration
  126174. seppelt
  126175. seppelt
  126176. konrad
  126177. fluorine
  126178. stabilized
  126179. sulfur
  126180. carbon
  126181. multiple
  126182. seppelt
  126183. konrad
  126184. structure
  126185. color
  126186. chemistry
  126187. pentaaryl
  126188. sequence
  126189. sequence-selective
  126190. sequence-specific
  126191. sequences
  126192. sequencing
  126193. sequential
  126194. sequential
  126195. photocycloaddition
  126196. rearrangement
  126197. subst
  126198. sequential
  126199. alkoxy
  126200. radical
  126201. fragmentation
  126202. cyclopropylcarbinyl
  126203. sequential
  126204. benzannulation
  126205. nucleophilic
  126206. aromatic
  126207. addition
  126208. sequential
  126209. cross-coupling
  126210. reactions
  126211. versatile
  126212. synthetic
  126213. sequential
  126214. reactions
  126215. annelaction
  126216. procedure
  126217. sequential
  126218. radical
  126219. macrocyclisation
  126220. transannulation
  126221. approach
  126222. sequential
  126223. expansion
  126224. ketene
  126225. elimination
  126226. reactions
  126227. sequential
  126228. promoted
  126229. electron
  126230. reactions
  126231. sequential
  126232. transformations
  126233. organic
  126234. chemistry
  126235. synthetic
  126236. serafino
  126237. serebryakov
  126238. seredkina
  126239. serendipity
  126240. serge
  126241. sergeev
  126242. sergeev
  126243. subbotin
  126244. spectroscopy
  126245. substituted
  126246. sergeev
  126247. shitikov
  126248. nedel'kin
  126249. arylene
  126250. sulphide
  126251. sergei
  126252. sergio
  126253. serhan
  126254. seriesQ
  126255. serinal
  126256. serine
  126257. serjeant
  126258. dempsey
  126259. ionization
  126260. constants
  126261. organic
  126262. acids
  126263. serotonin
  126264. serotonin-3
  126265. serov
  126266. serpone
  126267. serpone
  126268. terzian
  126269. lawless
  126270. darren
  126271. herrmann
  126272. marie
  126273. serrano
  126274. serratosa
  126275. sertraline
  126276. serum/urine
  126277. servi
  126278. services
  126279. sesbanimide
  126280. seshimoto
  126281. sesquicentenary
  126282. sesquifulvalenes
  126283. sesquiterpene
  126284. sesquiterpenes
  126285. sesquiterpenoids[
  126286. sesquiterpenoids
  126287. sessler
  126288. sessler
  126289. burrell
  126290. sapphyrins
  126291. sessler
  126292. burrell
  126293. sapphyrns
  126294. sessler
  126295. jonathan
  126296. michael
  126297. furuta
  126298. hiroyuki
  126299. vladimir
  126300. sessler
  126301. jonathan
  126302. hemmi
  126303. gregory
  126304. tarak
  126305. murai
  126306. toshiaki
  126307. sesterterpenes
  126308. sesterterpenoidsZ
  126309. setkina
  126310. setsuko
  126311. setsune
  126312. setsuo
  126313. setting
  126314. seven
  126315. seven-membered
  126316. seven-membered
  126317. rings
  126318. heteroatoms
  126319. seven-memebered
  126320. seventy
  126321. several
  126322. severin
  126323. sexsmith
  126324. sextet
  126325. sexual
  126326. seyam
  126327. seyden
  126328. seyden
  126329. penne
  126330. selective
  126331. carbanion
  126332. chemistry
  126333. anion
  126334. catio
  126335. seyden
  126336. penne
  126337. jacqueline
  126338. reductions
  126339. alumino
  126340. borohy
  126341. seyferth
  126342. seyhold
  126343. seymour
  126344. shaban
  126345. shaban
  126346. mohammed
  126347. mamdouh
  126348. sharshira
  126349. essam
  126350. synth
  126351. shafiee
  126352. shafii
  126353. shafran
  126354. shahrokh
  126355. shaik
  126356. shaik
  126357. sason
  126358. schlegel
  126359. bernhard
  126360. wolfe
  126361. theoretical
  126362. shainyan
  126363. shainyan
  126364. mirskova
  126365. carbon
  126366. nitrogen
  126367. triad
  126368. prototro
  126369. shambayati
  126370. shamma
  126371. shamma
  126372. hindenlang
  126373. carbon
  126374. shift
  126375. assignments
  126376. shamma
  126377. moniot
  126378. isoquinoline
  126379. alkaloids
  126380. research
  126381. shamsevaleev
  126382. shankar
  126383. shannon
  126384. shanro
  126385. shanzer
  126386. shanzer
  126387. yakirevitch
  126388. gottlieb
  126389. libman
  126390. polytopic
  126391. shapakin
  126392. shape
  126393. shape
  126394. chemistry
  126395. introduc
  126396. molecular
  126397. shape
  126398. shape-conformation
  126399. shaped
  126400. shapes
  126401. shapiro
  126402. shapiro
  126403. dyatkin
  126404. nefedov
  126405. carbene
  126406. reactions
  126407. shapiro
  126408. polyols
  126409. unique
  126410. class
  126411. compound
  126412. russian
  126413. shapley
  126414. sharma
  126415. sharma
  126416. thiophosgene
  126417. organic
  126418. synthesis
  126419. synthesi
  126420. sharpless
  126421. verhoeven
  126422. selective
  126423. oxygenation
  126424. sharpless
  126425. barry
  126426. coelacanths
  126427. catalysis
  126428. tetrahedron
  126429. sharpless's
  126430. sharshira
  126431. sharts
  126432. shaum
  126433. shaun
  126434. shawali
  126435. shawali
  126436. ahmad
  126437. reactions
  126438. heterocyclic
  126439. compounds
  126440. shchegolev
  126441. shchelokhova
  126442. shcherbakova
  126443. recent
  126444. developments
  126445. synthesis
  126446. structure
  126447. sheet
  126448. sheets
  126449. sheikh
  126450. sheinker
  126451. sheinker
  126452. garnovskii
  126453. osipov
  126454. advances
  126455. study
  126456. shekell
  126457. sheldon
  126458. sheldon
  126459. sheldon
  126460. homogeneous
  126461. heterogeneous
  126462. catalytic
  126463. oxidatio
  126464. sheldon
  126465. kochi
  126466. metal
  126467. catalyzed
  126468. oxidations
  126469. organic
  126470. sheldon
  126471. roger
  126472. chirotechnology
  126473. industrial
  126474. synthesis
  126475. sheldon
  126476. roger
  126477. organic
  126478. synthesis
  126479. present
  126480. future
  126481. sheldrake
  126482. sheldrick
  126483. sheldrick
  126484. stereochemistry
  126485. penta
  126486. hexacoordinate
  126487. shelf
  126488. shell
  126489. shellfish
  126490. sheludyakov
  126491. sheludyakov
  126492. mironov
  126493. organosilicon
  126494. carbonates
  126495. sheng
  126496. shenna
  126497. shepherd
  126498. shepherd
  126499. cyclobutarenes
  126500. chemistry
  126501. benzocyclobuten
  126502. sheppard
  126503. sheppard
  126504. partial
  126505. synthesis
  126506. peptides
  126507. proteins
  126508. sheri
  126509. sheridan
  126510. sherif
  126511. sherington
  126512. sherle
  126513. shermaQ
  126514. sherman|
  126515. shermolovich
  126516. sherri
  126517. sherrington
  126518. sherrod
  126519. sherwood
  126520. shevchenko
  126521. shevchenko
  126522. apushkinskii
  126523. quinone
  126524. methides
  126525. shevelev
  126526. shevko
  126527. shevlin
  126528. shevlin
  126529. preparation
  126530. reactions
  126531. atomic
  126532. carbon
  126533. shiba
  126534. shibata
  126535. shibata
  126536. ikuya
  126537. organotin
  126538. enolates
  126539. organic
  126540. synthe
  126541. shibuya
  126542. shida
  126543. shield
  126544. shielded
  126545. shift
  126546. shifts
  126547. shigeru
  126548. shigeru
  126549. shiitake
  126550. shikimate
  126551. shikimic
  126552. shikimic
  126553. metabolism
  126554. metabolites
  126555. shilov
  126556. shilov
  126557. dinitrogen
  126558. fixation
  126559. solution
  126560. presence
  126561. shilov
  126562. shul'pin
  126563. activation
  126564. carbon
  126565. hydrogen
  126566. shilovskii
  126567. shima
  126568. shimizu
  126569. shimizu
  126570. nobujiro
  126571. silicon
  126572. effects
  126573. solvolysis
  126574. related
  126575. shimohigashi
  126576. shimokawa
  126577. shimomura
  126578. shine
  126579. shinhama
  126580. shinichi
  126581. shinichiro
  126582. shinkai
  126583. shinkai
  126584. bhupathy
  126585. chemoenzymic
  126586. synthesis
  126587. novel
  126588. shinkai
  126589. ichiro
  126590. practical
  126591. asymmetric
  126592. synthesis
  126593. novel
  126594. shinkai
  126595. ichiro
  126596. sigal
  126597. nolan
  126598. chemistry
  126599. biology
  126600. shinkai
  126601. functionalization
  126602. crown
  126603. ethers
  126604. calixarenes
  126605. shinkai
  126606. seiji
  126607. calixarenes
  126608. third
  126609. supramolecular
  126610. shinkai
  126611. seiji
  126612. calixarenes
  126613. third
  126614. generation
  126615. supramolec
  126616. shinsaku
  126617. shinya
  126618. shinzi
  126619. shioiri
  126620. shioiri
  126621. matsuura
  126622. hamada
  126623. groups
  126624. shionoya
  126625. shiozawa
  126626. shipchandler
  126627. shipchandler
  126628. utility
  126629. nitroacetic
  126630. shipov
  126631. shirley
  126632. shiro
  126633. shiroshi
  126634. shiroshita
  126635. shirwaikar
  126636. shishkina
  126637. shishkina
  126638. berezhnaya
  126639. photochemistry
  126640. dialkyl
  126641. shitikov
  126642. shizuka
  126643. shizuka
  126644. haruo
  126645. intramolecular
  126646. charge
  126647. transfer
  126648. emission
  126649. shklover
  126650. shklover
  126651. struchkov
  126652. structure
  126653. organocyclosilo
  126654. shkol'nikova
  126655. shmaryahu
  126656. shmaryhau
  126657. shnitko
  126658. shobana
  126659. shockman
  126660. shockor
  126661. shoji
  126662. shokol
  126663. shono
  126664. shono
  126665. tatsuya
  126666. electroorganic
  126667. synthesis
  126668. academic
  126669. london
  126670. shoolery
  126671. shore
  126672. shore
  126673. pauson
  126674. khand
  126675. cycloaddition
  126676. reaction
  126677. short
  126678. stereoselective
  126679. synthesis
  126680. dihydrosesamin
  126681. short
  126682. contact
  126683. reactions
  126684. large
  126685. organic
  126686. radicals
  126687. short
  126688. interactions
  126689. between
  126690. heterocyclic
  126691. sulfur
  126692. atoms
  126693. short
  126694. synthesis
  126695. dynemicin
  126696. structure
  126697. unusual
  126698. shorter
  126699. shreeve
  126700. shreeve
  126701. tetracoordinate
  126702. fluorosulfur
  126703. shriner
  126704. shriver
  126705. shtefan
  126706. shteingarts
  126707. shuan
  126708. shubin
  126709. shudo
  126710. shuji
  126711. shukla
  126712. shul'pin
  126713. shunichi
  126714. shunji
  126715. shusherina
  126716. shuttle
  126717. shvachkin
  126718. shvekhgeimer
  126719. shvetsov
  126720. shyamal
  126721. shono
  126722. tatsuya
  126723. electroorganic
  126724. synthesis
  126725. academic
  126726. london
  126727. short
  126728. stereoselective
  126729. synthesis
  126730. dihydrosesamin
  126731. siegel
  126732. wimmele
  126733. synthesis
  126734. intermediates
  126735. rhodium
  126736. sigma-organoplatinum
  126737. compounds
  126738. signal@
  126739. silanes
  126740. silicon
  126741. containing
  126742. carbonyl
  126743. equivalents@
  126744. siliranes@
  126745. siloxycyclopropanes
  126746. silyl
  126747. silylformylation
  126748. simple
  126749. simple
  126750. relationships
  126751. between
  126752. carbocation
  126753. lifetime
  126754. singh
  126755. vinod
  126756. practical
  126757. useful
  126758. methods
  126759. enantiose@
  126760. kaminsky
  126761. ziegler
  126762. natta
  126763. catalysis
  126764. advances
  126765. situ-generated@
  126766. six-membered
  126767. sladkov
  126768. gol'ding
  126769. reactions
  126770. copper
  126771. silver
  126772. orga@
  126773. small
  126774. smithers@
  126775. kenso
  126776. seiji
  126777. enantioselective
  126778. addition
  126779. organozin@
  126780. society
  126781. sogani@
  126782. solenolide@
  126783. solid
  126784. supports
  126785. catalysts
  126786. organic
  126787. synthesis@
  126788. solution
  126789. solvating@
  126790. shyamal
  126791. shyamali
  126792. shyamaprosad
  126793. si-m'-ge
  126794. sialic
  126795. sialic
  126796. derivatives
  126797. glycolipoids
  126798. sialo-compounds
  126799. sialosides
  126800. sialyl
  126801. chemistry
  126802. methoxy
  126803. methylamides
  126804. applications
  126805. sibille
  126806. sibiryak
  126807. membered
  126808. mesoionic
  126809. heterocycles
  126810. quinodimethane
  126811. sickinger
  126812. sidduri
  126813. side}
  126814. reactions
  126815. aromatic
  126816. nitration
  126817. synthetic
  126818. aspects
  126819. reactions
  126820. peptide
  126821. synthesis
  126822. side-chains
  126823. sidearms
  126824. sidechains
  126825. siderophores
  126826. sieber
  126827. siebert
  126828. siebert
  126829. boron
  126830. heterocycles
  126831. ligands
  126832. transition
  126833. metal
  126834. siebert
  126835. sandwich
  126836. triple
  126837. decker
  126838. organometallic
  126839. siedle
  126840. siegel
  126841. siegel
  126842. wimmele
  126843. synthesis
  126844. intermediates
  126845. rhodium
  126846. siegemund
  126847. sieger
  126848. siegfried
  126849. siegrist
  126850. sieve
  126851. sievers
  126852. sieves
  126853. sigal
  126854. sigel
  126855. sigeru
  126856. siggel
  126857. sigma
  126858. sigma
  126859. pi-rearrangements
  126860. organotransition
  126861. metal
  126862. compounds
  126863. sigma-bonded
  126864. sigma-bonded
  126865. organic
  126866. derivatives
  126867. elements
  126868. sigma-bonds
  126869. sigma-organocobalt
  126870. sigma-organocobalt
  126871. compounds
  126872. sigma-organoiridium
  126873. sigma-organoiridium
  126874. compounds
  126875. sigma-organoiron
  126876. sigma-organoiron
  126877. compounds
  126878. sigma-organomanganes
  126879. sigma-organomanganes
  126880. compounds
  126881. sigma-organonickel
  126882. sigma-organonickel
  126883. compounds
  126884. sigma-organoosmium
  126885. sigma-organoosmium
  126886. compounds
  126887. sigma-organopalladiu
  126888. sigma-organopalladiu
  126889. compounds
  126890. sigma-organoplatinum
  126891. sigma-organoplatinum
  126892. compounds
  126893. sigma-organoplatinum
  126894. compounds
  126895. sigma-organorhenium
  126896. sigma-organorhenium
  126897. pounds
  126898. sigma-organorhodium
  126899. sigma-organorhodium
  126900. compounds
  126901. sigma-organorutheniu
  126902. sigma-organorutheniu
  126903. compounds
  126904. sigmatropic
  126905. signalling
  126906. significance
  126907. silabenzene
  126908. silacyclopentane
  126909. silaethylenes
  126910. silafunctional
  126911. silane
  126912. silane
  126913. blocking
  126914. agents
  126915. silane
  126916. coupling
  126917. agent
  126918. chemistry
  126919. silane
  126920. coupling
  126921. reagents
  126922. silane-terminated
  126923. silanes
  126924. silanes
  126925. silanols
  126926. silaorganometallic
  126927. silatrane
  126928. silatranes
  126929. silatropic
  126930. silene
  126931. silene-t
  126932. silenes
  126933. silicaH
  126934. silica
  126935. supported
  126936. borohydride
  126937. novel
  126938. reagent
  126939. silicates
  126940. silicon
  126941. mistry
  126942. silicon
  126943. containing
  126944. carbonyl
  126945. equivalents
  126946. silicon
  126947. effects
  126948. electron-transfer
  126949. reactions
  126950. silicon-su
  126951. silicon
  126952. effects
  126953. solvolysis
  126954. related
  126955. reactions
  126956. silicon
  126957. hydrides
  126958. organic
  126959. synthesis
  126960. silicon
  126961. organic
  126962. sythesis
  126963. silicon
  126964. reagents
  126965. organic
  126966. synthesis
  126967. silicon
  126968. reagents
  126969. organic
  126970. synth
  126971. silicon
  126972. stabilization
  126973. silicon
  126974. ylide
  126975. chemistry
  126976. silicon-carbon
  126977. silicon-containing
  126978. silicon-containing
  126979. 13-alkenynes
  126980. unsaturated
  126981. compoun
  126982. silicon-heteroatom
  126983. silicon-hydrogen
  126984. silicon-mediated
  126985. silicon-mediated
  126986. stereochemically
  126987. controlled
  126988. reactions
  126989. silicon-silicon
  126990. silicon-substituted
  126991. silicone
  126992. silicone
  126993. organic
  126994. synthesis
  126995. silirene
  126996. siloxane
  126997. siloxane-tethered
  126998. siloxanes
  126999. siloxanes
  127000. temporary
  127001. tethers
  127002. photocycloadditions
  127003. siloxy
  127004. siloxy
  127005. dienes
  127006. total
  127007. synthesis
  127008. siloxycyclopropanes
  127009. siloxycyclopropanes
  127010. siloxycyclopropanes
  127011. useful
  127012. synthetic
  127013. intermediates
  127014. siloxydiene
  127015. silva
  127016. silvana
  127017. silver
  127018. silver
  127019. catalyzed
  127020. heterocyclization
  127021. first
  127022. total
  127023. synthesis
  127024. silver
  127025. oxide
  127026. assisted
  127027. palladium
  127028. catalyzed
  127029. cross
  127030. coupling
  127031. silverstein
  127032. silvester
  127033. silvester
  127034. michael
  127035. fluoroheterocyclic
  127036. compounds
  127037. synthesis
  127038. silvester
  127039. michael
  127040. landmarks
  127041. organofluorine
  127042. chemistry
  127043. silvester
  127044. michael
  127045. recent
  127046. advances
  127047. fluoro
  127048. heterocyclic
  127049. silvestre
  127050. silvio
  127051. silwa
  127052. silyl
  127053. silyl
  127054. ether
  127055. organic
  127056. synthesis
  127057. review
  127058. silyl
  127059. ethers
  127060. synthesis
  127061. silyl
  127062. ethers
  127063. synthesis
  127064. silyl
  127065. esters
  127066. phosph
  127067. rus-common
  127068. intermediates
  127069. synthesis
  127070. silyl
  127071. ethers
  127072. protective
  127073. groups
  127074. alcohols
  127075. oxidative
  127076. silyl
  127077. substituted
  127078. conjugated
  127079. dienes
  127080. review
  127081. silyl-substituted
  127082. silyl-substituted
  127083. conjugated
  127084. dienes
  127085. versatile
  127086. building
  127087. block
  127088. silyl-substituted
  127089. cyclopropanes
  127090. versatile
  127091. hetic
  127092. reage
  127093. silylamines
  127094. silylaminoenones
  127095. silylated
  127096. silylated
  127097. synthons
  127098. silylating
  127099. silylation
  127100. silylation
  127101. alkenenitriles
  127102. alkenenitriles
  127103. silylcarbinols
  127104. silylcarbocyclizatio
  127105. silylcuprate
  127106. silylcyclopropanes
  127107. silylene
  127108. silylenes
  127109. silylethers
  127110. silylformylation
  127111. silylformylation
  127112. silylhydroformylatio
  127113. silylhydroxylamines
  127114. silylhydroxylamines
  127115. compounds
  127116. unusual
  127117. nitrogen
  127118. coordina
  127119. silylmetallation
  127120. silylmethyl
  127121. silyloxiranes
  127122. silyloxy
  127123. simandi
  127124. simandi
  127125. barna
  127126. szeverenyi
  127127. nemeth
  127128. homogeneous
  127129. cataly
  127130. simanek
  127131. simchen
  127132. similar
  127133. similarities
  127134. similarity
  127135. simkinO
  127136. simkin
  127137. minkin
  127138. glukhovtsev
  127139. concept
  127140. aromat
  127141. simmons
  127142. simmons-smith
  127143. simon
  127144. simoneau
  127145. simonet
  127146. simonetta
  127147. simonoff
  127148. simonov
  127149. simonova
  127150. simonova
  127151. nefedov
  127152. toropova
  127153. kirillov
  127154. current
  127155. simons
  127156. simonyi
  127157. simonyi
  127158. chiral
  127159. molecules
  127160. akademiai
  127161. kiado
  127162. budapest
  127163. hunga
  127164. simpkins
  127165. simpkins
  127166. nigel
  127167. sulphones
  127168. organic
  127169. synthesis
  127170. tetrahedron
  127171. simple
  127172. simple
  127173. simple
  127174. effective
  127175. approaches
  127176. coumestans
  127177. azacoumest
  127178. simple
  127179. carbohydrates
  127180. starting
  127181. materials
  127182. organic
  127183. synthe
  127184. simple
  127185. enols
  127186. simple
  127187. yield
  127188. synthesis
  127189. unsymmetrically
  127190. functionalize
  127191. simple
  127192. indolizidine
  127193. alkaloids
  127194. simple
  127195. method
  127196. controlling
  127197. stereoselection
  127198. mannich
  127199. simple
  127200. methods
  127201. preparation
  127202. cryptands
  127203. simple
  127204. organometallic
  127205. reagents
  127206. elaboration
  127207. simple
  127208. methods
  127209. synthesis
  127210. carbonyl
  127211. compounds
  127212. simple
  127213. relationships
  127214. between
  127215. carbocation
  127216. lifetime
  127217. simplex
  127218. simplicity
  127219. simplified
  127220. simpson
  127221. simpson
  127222. biosynthesis
  127223. polyketides
  127224. natural
  127225. applications
  127226. marine
  127227. simulati
  127228. simulati
  127229. peptide
  127230. conformational
  127231. dynamics
  127232. thermodyn
  127233. simulating
  127234. simulation
  127235. simulations
  127236. sinay
  127237. sinay
  127238. pierre
  127239. recent
  127240. advances
  127241. glycosylation
  127242. reactions
  127243. since
  127244. sinchai
  127245. sinclair
  127246. sinegovskaya
  127247. sinev
  127248. singaram
  127249. singer
  127250. singh
  127251. singh
  127252. nakshatra
  127253. singh
  127254. singh
  127255. narendra
  127256. organic
  127257. solid
  127258. singh
  127259. parmar
  127260. raman
  127261. stenberg
  127262. chemistry
  127263. singh
  127264. sternberg
  127265. parmar
  127266. photochemistry
  127267. alkaloi
  127268. singh
  127269. vinod
  127270. practical
  127271. useful
  127272. methods
  127273. enantiose
  127274. single
  127275. single
  127276. double
  127277. nucleophilic
  127278. addition
  127279. coordinated
  127280. hydro
  127281. single
  127282. electron
  127283. transfer
  127284. review
  127285. single
  127286. electron
  127287. transfer
  127288. nucleophilic
  127289. substitution
  127290. single
  127291. electron-transfer
  127292. processes
  127293. perfluoroalkyl
  127294. halide
  127295. single-electron
  127296. single-electron
  127297. transfer
  127298. major
  127299. reaction
  127300. pathway
  127301. organic
  127302. singlet
  127303. singlet
  127304. methylcarbene
  127305. equilibrium
  127306. geometry
  127307. transition
  127308. singlet
  127309. oxygen
  127310. singlet
  127311. oxygen
  127312. organic
  127313. synthesis
  127314. singleton
  127315. sinha
  127316. sinha
  127317. regioselective
  127318. catalysts
  127319. sinha
  127320. technical
  127321. services
  127322. sinkovic
  127323. kaminsky
  127324. ziegler
  127325. natta
  127326. catalysis
  127327. advances
  127328. sinnott
  127329. sinotova
  127330. sinta
  127331. sinyashin
  127332. sirenin
  127333. siskin
  127334. siskin
  127335. michael
  127336. katritzky
  127337. reactivity
  127338. organic
  127339. compou
  127340. lawrence
  127341. heavy
  127342. metal
  127343. organic
  127344. chemistry
  127345. building
  127346. selective
  127347. formation
  127348. valent
  127349. titanium
  127350. reagents
  127351. selective
  127352. hydrogen
  127353. metal
  127354. exchange
  127355. competition
  127356. coope
  127357. selectivity
  127358. crucial
  127359. intermediates
  127360. reactions
  127361. sites
  127362. sivaram
  127363. six-membered
  127364. six-membered
  127365. six-membered
  127366. rings
  127367. oxygen
  127368. sulfur
  127369. sixfold
  127370. sixty
  127371. sized
  127372. sizov
  127373. skancke
  127374. skarchenko
  127375. skarchenko
  127376. oxidative
  127377. dehydrogenation
  127378. hydrocarbons
  127379. skeleta
  127380. skeletal
  127381. skeletal
  127382. rearrangements
  127383. organoalkali
  127384. metal
  127385. pounds
  127386. skeletal
  127387. reorganizations
  127388. chain
  127389. extension
  127390. expansion
  127391. skeleton
  127392. skeletons
  127393. skell
  127394. skell
  127395. ground
  127396. state
  127397. excited
  127398. state
  127399. chemistry
  127400. skerlj
  127401. skipped
  127402. skonieczny
  127403. skonieczny
  127404. reactions
  127405. acridine
  127406. derivatives
  127407. skorobogatova
  127408. skraup
  127409. skrunts
  127410. skvortsov
  127411. skvortsov
  127412. advances
  127413. study
  127414. stereochemistry
  127415. sladkov
  127416. sladkov
  127417. gol'ding
  127418. reactions
  127419. copper
  127420. silver
  127421. slavenuiter
  127422. slippage
  127423. sliskovic
  127424. slivinskii
  127425. sliwa
  127426. sliwa
  127427. phenantbroline
  127428. complexes
  127429. sliwa
  127430. cycloaddition
  127431. reactions
  127432. pyridines
  127433. sliwa
  127434. zamarlik
  127435. polyazaphenanthrenes
  127436. heterocy
  127437. sliwa
  127438. wanda
  127439. bachowska
  127440. barbara
  127441. zelichowicz
  127442. natalia
  127443. chemistry
  127444. sliwa
  127445. wanda
  127446. chrzastek
  127447. lidia
  127448. mielniczak
  127449. marian
  127450. guest
  127451. sliwa
  127452. wanda
  127453. reactivity
  127454. acridinium
  127455. salts
  127456. related
  127457. slotin
  127458. slough
  127459. slowed
  127460. slowed
  127461. tripodal
  127462. rotation
  127463. arene-chromium
  127464. complexes
  127465. steric
  127466. sm/smi2
  127467. smadja
  127468. smadja
  127469. william
  127470. acyclic
  127471. diastereofacial
  127472. selection
  127473. intermol
  127474. small
  127475. small
  127476. small
  127477. strained
  127478. cyclophanes
  127479. small
  127480. carboranes
  127481. building
  127482. blocks
  127483. designed
  127484. organometall
  127485. small
  127486. cyclophanes
  127487. benzene
  127488. business
  127489. small
  127490. molecule
  127491. potential
  127492. oxalyl
  127493. chloride
  127494. small
  127495. compounds
  127496. containing
  127497. sulfur
  127498. atoms
  127499. small
  127500. compounds
  127501. organic
  127502. synthesis
  127503. small
  127504. propellanes
  127505. small-ring
  127506. small-ring
  127507. organo-silicon
  127508. germanium
  127509. ompounds
  127510. smalley
  127511. smalley
  127512. assembly
  127513. fullerenes
  127514. smalley
  127515. halogenoquinolines
  127516. quinoline
  127517. derivatives
  127518. smalley
  127519. chemistry
  127520. indoxazenes
  127521. anthranils
  127522. smallridge
  127523. smeby
  127524. smeby
  127525. fermandjian
  127526. conformation
  127527. angiotensin
  127528. chemi
  127529. smeets
  127530. smegel
  127531. smell
  127532. induced
  127533. asymmetric
  127534. reduction
  127535. benzil
  127536. presence
  127537. mediated
  127538. reductive
  127539. addition
  127540. phenylsulfones
  127541. smi2-promoted
  127542. smiles
  127543. smirnov
  127544. smirnova
  127545. zefirov
  127546. bodrikov
  127547. krimer
  127548. episulfonium
  127549. smith
  127550. smith
  127551. dieter
  127552. promoted
  127553. decomposition
  127554. smith
  127555. transformations
  127556. phosphorus
  127557. stabilized
  127558. anions
  127559. smith
  127560. diane
  127561. supramolecular
  127562. chemistry
  127563. chemistry
  127564. industr
  127565. smith
  127566. solid
  127567. supports
  127568. catalysts
  127569. organic
  127570. synthesis
  127571. smith
  127572. protoporphyrin
  127573. recent
  127574. research
  127575. smith
  127576. michael
  127577. compendium
  127578. organic
  127579. synthetic
  127580. methods
  127581. smith
  127582. robin
  127583. vellekoop
  127584. samuel
  127585. addition
  127586. reactions
  127587. smithers
  127588. smithrud
  127589. smoke
  127590. smsov
  127591. additions
  127592. organocopper
  127593. reagents
  127594. vinyloxiranes
  127595. approaches
  127596. organocopper
  127597. reagents
  127598. vinyl
  127599. oxiranes
  127600. prime
  127601. addition
  127602. organo
  127603. copper
  127604. reagents
  127605. tovinyl
  127606. oxirane
  127607. sn2-type
  127608. sncl4
  127609. snider
  127610. snider
  127611. lewis
  127612. catalyzed
  127613. reactions
  127614. snider
  127615. barry
  127616. carbofunctionalizati
  127617. alkenes
  127618. chemtracts
  127619. snieckus
  127620. snieckus
  127621. combined
  127622. directed
  127623. ortho
  127624. metalation
  127625. cross
  127626. coupling
  127627. snieckus
  127628. heterocyclic
  127629. compounds
  127630. alkaloid
  127631. synthesis
  127632. snieckus
  127633. streith
  127634. diazepines
  127635. vista
  127636. heterocycl
  127637. sns2-xsex
  127638. snyder
  127639. kenso
  127640. seiji
  127641. enantioselective
  127642. addition
  127643. organozin
  127644. sobenina
  127645. sobolev
  127646. soccer-ball
  127647. soccolini
  127648. social
  127649. societe
  127650. society
  127651. society
  127652. sodano
  127653. sodeau
  127654. sodeau
  127655. photoreactions
  127656. formaldehyde
  127657. soderquist
  127658. soderquist
  127659. samarium
  127660. iodide
  127661. organic
  127662. synthesis
  127663. sodium
  127664. sodium
  127665. cyanoborohydride
  127666. highly
  127667. effective
  127668. reducing
  127669. agent
  127670. sodium
  127671. trimethylsilanethiol
  127672. novel
  127673. cyclizations
  127674. synthe
  127675. sodium/mercury
  127676. soedin
  127677. sogani
  127678. soichi
  127679. sojka
  127680. sokolov
  127681. sokolov
  127682. aleksandrov
  127683. organic
  127684. peroxides
  127685. alkali
  127686. sokolov
  127687. advances
  127688. chemistry
  127689. azoles
  127690. sokolov
  127691. stankevich
  127692. fullerenes
  127693. allotropic
  127694. sokolov
  127695. viatcheslav
  127696. chirality
  127697. optical
  127698. activity
  127699. sokolov
  127700. viatcheslav
  127701. introduction
  127702. theoretical
  127703. stereochem
  127704. sokolovskii
  127705. sokolyanskaya
  127706. sokolyuk
  127707. sokolyuk
  127708. romanov
  127709. pisulina
  127710. naphthacenequinones
  127711. solamin
  127712. solanum
  127713. solar
  127714. soldatenkov
  127715. solid
  127716. solid
  127717. phase
  127718. peptite
  127719. synthesis
  127720. practical
  127721. approach
  127722. solid
  127723. state
  127724. chemistry
  127725. molecular
  127726. metal
  127727. oxide
  127728. clusters
  127729. solid
  127730. state
  127731. organic
  127732. reactions
  127733. solid
  127734. supports
  127735. catalysts
  127736. organic
  127737. synthesis
  127738. solid-phase
  127739. solid-phase
  127740. solution
  127741. segment
  127742. condensation
  127743. peptide
  127744. synthe
  127745. solid-state
  127746. solid-supported
  127747. solid-supported
  127748. oxidants
  127749. solids
  127750. soline
  127751. solladie
  127752. solladie
  127753. antonio
  127754. carmen
  127755. asymmetric
  127756. synthesis
  127757. natura
  127758. solladie
  127759. asymmetric
  127760. synthesis
  127761. using
  127762. nucleophilic
  127763. reagents
  127764. solodenko
  127765. solodovnikov
  127766. solodovnikov
  127767. bubnov
  127768. prokof'ef
  127769. stereochemistry
  127770. soloshonok
  127771. solouki
  127772. solov'ev
  127773. solov'ev
  127774. kadentsev
  127775. chizhov
  127776. spectrometry
  127777. solov'eva
  127778. solov'yanov
  127779. solov'yanov
  127780. beletskaya
  127781. reactivity
  127782. carbanions
  127783. solubilities
  127784. solubility
  127785. soluble
  127786. solutes
  127787. solution
  127788. solution
  127789. solution
  127790. structure
  127791. lithio
  127792. dithianes
  127793. solution
  127794. complex
  127795. stereochemical
  127796. problems
  127797. solution
  127798. phase
  127799. chemistry
  127800. radical
  127801. cations
  127802. solution
  127803. spray
  127804. flash
  127805. vacuum
  127806. pyrolysis
  127807. method
  127808. prepar
  127809. solution
  127810. structure
  127811. allenyl
  127812. propargyllithium
  127813. reagents
  127814. solution
  127815. structures
  127816. lithium
  127817. dialkylamides
  127818. related
  127819. solution
  127820. thermodynamics
  127821. amino
  127822. acid-18
  127823. crown
  127824. amino
  127825. solutions
  127826. solvated
  127827. solvating
  127828. solvation
  127829. solvation
  127830. electrophilic
  127831. driving
  127832. force
  127833. ionic
  127834. brominati
  127835. solvatochromic
  127836. solvatochromism
  127837. solvent
  127838. decarbonylation
  127839. radicals
  127840. studi
  127841. solvent
  127842. effects
  127843. molecular
  127844. recognition
  127845. solvent
  127846. effects
  127847. hetero
  127848. diels
  127849. alder
  127850. reactions
  127851. sulfur
  127852. solvent
  127853. effects
  127854. mechanism
  127855. selectivities
  127856. asymme
  127857. solvent
  127858. effects
  127859. opening
  127860. cyclopropanones
  127861. solvent
  127862. pressure
  127863. effects
  127864. radical
  127865. reactions
  127866. reconci
  127867. solvent-induced
  127868. solvent-induced
  127869. changes
  127870. selectivity
  127871. solvolyses
  127872. solvents
  127873. solvents
  127874. solvents
  127875. solvent
  127876. effects
  127877. organic
  127878. chemistry
  127879. solving
  127880. solvolyses
  127881. solvolysis
  127882. solvolytic
  127883. solvomercuration-dem
  127884. solvomercuration-dem
  127885. reactions
  127886. aminophosphinocarbox
  127887. acids
  127888. their
  127889. derivatives
  127890. applications
  127891. metal
  127892. carbonyl
  127893. anions
  127894. synthesis
  127895. applications
  127896. chloride
  127897. synthetic
  127898. organic
  127899. aspects
  127900. biocatalysis
  127901. organic-solvents
  127902. aspects
  127903. nometallic
  127904. chemistry
  127905. non-transition
  127906. aspects
  127907. silicon
  127908. radical
  127909. chemistry
  127910. aspects
  127911. chemistry
  127912. biological
  127913. activity
  127914. aspects
  127915. organic
  127916. chemistry
  127917. cobalt
  127918. aspects
  127919. reactivity
  127920. hypervalent
  127921. species
  127922. chemistry
  127923. hindered
  127924. organoboranes
  127925. chemistry
  127926. pentakis
  127927. methoxycarbonyl
  127928. cyclopentadiene
  127929. chiral
  127930. approaches
  127931. syntheses
  127932. bioactive
  127933. indolizidin
  127934. elecrophilic
  127935. fluorination
  127936. agents
  127937. aspects
  127938. hydroxamic
  127939. acids
  127940. chemistry
  127941. concepts
  127942. chemistry
  127943. p-block
  127944. elements
  127945. strategies
  127946. protection
  127947. activation
  127948. direction
  127949. observations
  127950. palladium
  127951. catalyzed
  127952. triflate
  127953. arene
  127954. carbon-carbon
  127955. formation
  127956. reacti
  127957. problems
  127958. stereochemistry
  127959. nitrogen
  127960. compounds
  127961. recent
  127962. advances
  127963. chemistry
  127964. imines
  127965. particula
  127966. recent
  127967. developments
  127968. synthetic
  127969. organic
  127970. sulfur
  127971. chemist
  127972. recent
  127973. synthetic
  127974. routes
  127975. thioketones
  127976. thioaldehyde
  127977. transformation
  127978. reactions
  127979. sulfur
  127980. containing
  127981. routes
  127982. sulfoxides
  127983. enantiomeric
  127984. studies
  127985. proximal
  127986. addition
  127987. elimination
  127988. procedures
  127989. studies
  127990. bromoethyl
  127991. iodoethyl
  127992. synthetically
  127993. useful
  127994. reactions
  127995. elemental
  127996. sulfur
  127997. silicone
  127998. compounds
  127999. organic
  128000. synthesis
  128001. somei
  128002. somers
  128003. sommelet
  128004. sommerfeld
  128005. somorjai
  128006. somsak
  128007. somsak
  128008. laszlo
  128009. ferrier
  128010. robert
  128011. radical
  128012. mediated
  128013. brominations
  128014. sonawane
  128015. sonawane
  128016. harikisan
  128017. bellur
  128018. nanjundiah
  128019. ahuja
  128020. jaimala
  128021. sonawane
  128022. harikisan
  128023. bellur
  128024. nanjundiah
  128025. kulkarni
  128026. dilip
  128027. soncini
  128028. sondheimer
  128029. sonnet
  128030. sonnet
  128031. olefin
  128032. inversion
  128033. tetrahedron
  128034. review
  128035. sonntag
  128036. sonochemical
  128037. sonochemical
  128038. cleavage
  128039. bromomethyl
  128040. aziridines
  128041. sonochemical
  128042. cleavage
  128043. bromomethyl
  128044. aziridine
  128045. sonochemistry
  128046. sonochemistry
  128047. ultrasound
  128048. chemistry
  128049. sonochemistry
  128050. theory
  128051. applications
  128052. ultrasound
  128053. sonochemistry-the
  128054. synthetically
  128055. useful
  128056. reactions
  128057. elemental
  128058. sulfur
  128059. sonochemistry-the
  128060. space@
  128061. spacers@
  128062. spatial@
  128063. species
  128064. spectrometric
  128065. spectroscopy
  128066. spiro
  128067. hepta-46-dienes
  128068. synthesis
  128069. chemical
  128070. reactions@
  128071. spirooxyphosphoranyl@
  128072. splitter
  128073. janet
  128074. turecek
  128075. frantisek
  128076. applications
  128077. spec@
  128078. sprintschnik@
  128079. squaraines@
  128080. stabilized
  128081. stancoviv
  128082. charles
  128083. schreiber
  128084. stuart
  128085. molecular
  128086. design
  128087. stanoeva
  128088. startsev@
  128089. state
  128090. stategies@
  128091. steckhan
  128092. electroenzymatic
  128093. synthesis
  128094. stemona@
  128095. intramoleular
  128096. diels-alder
  128097. reac@
  128098. stereochemistry@
  128099. stereochemistry
  128100. sigmatropic
  128101. rearrangements@
  128102. stereochemistry
  128103. thermolytic
  128104. catalysed
  128105. decarboxylatio@
  128106. stereocontrolled
  128107. 5-exo-trig
  128108. cyclization
  128109. imidoyl
  128110. radicals
  128111. stereoconvergent
  128112. tandem
  128113. wittig
  128114. anionic
  128115. sonochemistry-the
  128116. sonochemistry-the
  128117. ultrasonic
  128118. waves
  128119. synthetic
  128120. organ
  128121. sonoda
  128122. sonoda
  128123. noboru
  128124. selenium
  128125. assistedcarbonylatio
  128126. carbon
  128127. electronic
  128128. structure
  128129. organic
  128130. conductors
  128131. sophisticated
  128132. sorba
  128133. sorbate
  128134. sorenson
  128135. sorokin
  128136. soroosh
  128137. sorrell
  128138. sosna
  128139. sosnovsky
  128140. soucek
  128141. soumillion
  128142. soumillion
  128143. philippe
  128144. photoinduced
  128145. electron
  128146. transfer
  128147. source
  128148. source
  128149. intramolecular
  128150. enzymatic
  128151. reactivity
  128152. sourcebook
  128153. sources
  128154. sources
  128155. strategies
  128156. formation
  128157. chiral
  128158. compounds
  128159. southon
  128160. sp2-carbanionic
  128161. space-filler-enes
  128162. spacer
  128163. spacers
  128164. spada
  128165. spagnolo
  128166. spande
  128167. spande
  128168. hydroxyindoles
  128169. indole
  128170. alcohols
  128171. indolethiols
  128172. spanget
  128173. spangler
  128174. spanning
  128175. spargo
  128176. spargo
  128177. organic
  128178. halides
  128179. contemporary
  128180. organic
  128181. synthesis
  128182. sparteine
  128183. sparteine-mediated
  128184. sparteine-mediated
  128185. a-lithiation
  128186. n-boc-n-methylbenzyl
  128187. special
  128188. features
  128189. synthesis
  128190. peptides
  128191. containing
  128192. special
  128193. polymers
  128194. polymers
  128195. condensed
  128196. heterocyclic
  128197. rings
  128198. speciality
  128199. speciest
  128200. species
  128201. specific
  128202. specific
  128203. interactions
  128204. intermolecular
  128205. forces
  128206. steric
  128207. requireme
  128208. specific
  128209. reactions
  128210. organylmetal
  128211. complexes
  128212. unsaturate
  128213. specifically
  128214. specification
  128215. specification
  128216. molecular
  128217. chirality
  128218. specificity
  128219. speckamp
  128220. speckamp
  128221. aspects
  128222. reactions
  128223. cations
  128224. radica
  128225. speckamp
  128226. recent
  128227. developments
  128228. alkaloid
  128229. synthesis
  128230. spectraL
  128231. spectral
  128232. spectral
  128233. structural
  128234. properties
  128235. heterocyclic
  128236. ketene
  128237. spectrometric
  128238. spectrometric
  128239. spectrometry
  128240. spectrophotometric
  128241. spectrophysics
  128242. spectroscopic
  128243. spectroscopies
  128244. spectroscopy
  128245. spectroscopy
  128246. spects
  128247. speculations
  128248. speier
  128249. speier
  128250. homogeneous
  128251. catalysis
  128252. hydrosilation
  128253. transit
  128254. spencer
  128255. spengler
  128256. speranza
  128257. speranza
  128258. maurizio
  128259. tritium
  128260. generation
  128261. carbocations
  128262. spermidine
  128263. spermine
  128264. spero
  128265. sphere
  128266. sphereelectrontransf
  128267. spheres
  128268. spherical
  128269. sphin-oxides
  128270. sphingosine
  128271. spiders
  128272. spielman
  128273. spillane
  128274. control
  128275. organic
  128276. molecules
  128277. spin-label
  128278. spin-spin
  128279. spinace
  128280. spinelli
  128281. spinpolycarbenes
  128282. spirans
  128283. spiro_
  128284. spiro
  128285. hepta
  128286. triene
  128287. spiro
  128288. hepta-46-dienes
  128289. synthesis
  128290. chemical
  128291. reactions
  128292. spiro-o-benzoquinone
  128293. spiroacetal
  128294. spiroacetals
  128295. spiroannelation
  128296. spiroannulation
  128297. spirobenzopyran
  128298. spirobenzylisoquinol
  128299. spiroconjugation
  128300. spirocyclic
  128301. spirocyclic
  128302. dipeptides
  128303. amino
  128304. cyclohexanecarboxyli
  128305. spirocyclization
  128306. spirocycloalkane
  128307. spirocycloheptadiene
  128308. spirocyclohexanes
  128309. spirodecane
  128310. spirodiaza
  128311. spiroheterocyclic
  128312. spiroheterocyclic
  128313. systems
  128314. substituted
  128315. spiroheterocycli
  128316. spiroimidazolones
  128317. spiroindolenine
  128318. spiroketal
  128319. spiroketal
  128320. equilibration
  128321. interconversion
  128322. dioxaspiro
  128323. spiroketal-containin
  128324. spiroketals
  128325. spirone
  128326. spiropyrans
  128327. spiropyrans
  128328. structural
  128329. features
  128330. photochemical
  128331. properties
  128332. spiropyrrolidines
  128333. spiros
  128334. splitter
  128335. splitter
  128336. janet
  128337. turecek
  128338. frantisek
  128339. applications
  128340. splitting
  128341. spoerri
  128342. sponge
  128343. sponge
  128344. phospholipids
  128345. sponge
  128346. sterols
  128347. origins
  128348. biosynthesis
  128349. sponges
  128350. spontaneous
  128351. sporn
  128352. sprague
  128353. spray
  128354. springerR
  128355. springerverlag
  128356. springs
  128357. sprintschnik
  128358. spunta
  128359. spurgeon
  128360. squalene
  128361. squalestatin
  128362. squalestatins
  128363. squire
  128364. squires
  128365. squires
  128366. robert
  128367. phase
  128368. carbanion
  128369. chemistry
  128370. 199225
  128371. srebnik
  128372. srinivas
  128373. srinivasan
  128374. reactions
  128375. iodobicyclo
  128376. 4.1.0
  128377. heptane
  128378. carbanion
  128379. stabilised
  128380. stabilised
  128381. vinyl
  128382. cations
  128383. stabilities
  128384. stability
  128385. stabilization
  128386. stabilization
  128387. reactive
  128388. aldehydes
  128389. complexation
  128390. stabilization-activa
  128391. stabilized
  128392. stabilized
  128393. stabilized
  128394. nucleophiles
  128395. electron
  128396. deficient
  128397. alkenes
  128398. stabilizing
  128399. stableJ
  128400. stacey
  128401. stack
  128402. stacking
  128403. stadlbauer
  128404. stadlbauer
  128405. wolfgang
  128406. kappe
  128407. thomas
  128408. simple
  128409. effective
  128410. approa
  128411. stadnichuk
  128412. stadnichuk
  128413. voropaeva
  128414. silicon
  128415. containing
  128416. alkenynes
  128417. stadtmueller
  128418. stage
  128419. stages
  128420. stahl
  128421. staib
  128422. staley
  128423. staley
  128424. dustman
  128425. carbanions
  128426. reactive
  128427. intermediate
  128428. stalick
  128429. stammer
  128430. stancoviv
  128431. stancoviv
  128432. charles
  128433. schreiber
  128434. stuart
  128435. molecular
  128436. design
  128437. standaert
  128438. standingx
  128439. stanek
  128440. stang
  128441. stang
  128442. rappoport
  128443. subramanian
  128444. hanack
  128445. vinyl
  128446. cations
  128447. stang
  128448. small
  128449. strained
  128450. compounds
  128451. unsaturated
  128452. stang
  128453. unsaturated
  128454. carbenes
  128455. chemical
  128456. reviews
  128457. stang
  128458. vinyl
  128459. triflate
  128460. chemistry
  128461. unsaturated
  128462. cations
  128463. stang
  128464. peter
  128465. alkynyl
  128466. alkenyl
  128467. phenyl
  128468. iodonium
  128469. compounds
  128470. stang
  128471. peter
  128472. alkynyl
  128473. carboxylate
  128474. phosphate
  128475. sulfonate
  128476. staninets
  128477. stanislav
  128478. stanislaw
  128479. stankevich
  128480. stanley
  128481. stannane
  128482. stannanes
  128483. stannyl
  128484. stannylacetylenes
  128485. stannylamines
  128486. stannylcyanocuprates
  128487. stannylenes
  128488. stanoeva
  128489. stanoeva
  128490. stanovnik
  128491. stanovnik
  128492. branko
  128493. dipolar
  128494. cycloadditions
  128495. diazoalkanes
  128496. stanton
  128497. starandsy
  128498. starburst
  128499. starburst
  128500. cascade
  128501. dendrimers
  128502. fundamental
  128503. building
  128504. blocks
  128505. starburst/cascade
  128506. starburst/cascade
  128507. dendrimers
  128508. fundamenta
  128509. building
  128510. blocks
  128511. starch
  128512. stark
  128513. starks
  128514. starks
  128515. liotta
  128516. phase
  128517. transfer
  128518. catalysis
  128519. academic
  128520. press
  128521. starks
  128522. charles
  128523. liotta
  128524. charles
  128525. halpern
  128526. phase
  128527. transfe
  128528. starodub
  128529. stars
  128530. start
  128531. starting
  128532. startsev
  128533. mechanism
  128534. hydrogenolysis
  128535. thiophene
  128536. state
  128537. state
  128538. stategies
  128539. employed
  128540. synthesis
  128541. prostacyclins
  128542. stategies
  128543. macrolide
  128544. synthesis
  128545. concise
  128546. approach
  128547. states
  128548. static
  128549. statine
  128550. stationary
  128551. statistical
  128552. status
  128553. stauber
  128554. stauber
  128555. margaret
  128556. debiak
  128557. krook
  128558. therese
  128559. miller
  128560. marvin
  128561. staudinger
  128562. staunton
  128563. stavaux
  128564. wojciech
  128565. andrzej
  128566. stereocontrolled
  128567. synthesis
  128568. steckhank
  128569. steckhan
  128570. electroenzymatic
  128571. synthesis
  128572. steel
  128573. steel
  128574. patrick
  128575. aldehydes
  128576. ketones
  128577. contemporary
  128578. organic
  128579. steele
  128580. steele
  128581. saturated
  128582. nitrogen
  128583. heterocycles
  128584. contemporary
  128585. steen
  128586. steer
  128587. steer
  128588. structure
  128589. decay
  128590. dynamics
  128591. electronic
  128592. excited
  128593. stefan
  128594. stefano
  128595. stegel
  128596. steggerda
  128597. steglich
  128598. stein
  128599. stein
  128600. stephen
  128601. thermal
  128602. reactions
  128603. properties
  128604. polycycl
  128605. steinborn
  128606. steinborn
  128607. influence
  128608. heteroatoms
  128609. alpha
  128610. steiner
  128611. stejskal
  128612. steliou
  128613. steliou
  128614. kosta
  128615. diatomic
  128616. sulfur
  128617. accts
  128618. research
  128619. stella
  128620. stemodane
  128621. stenberg
  128622. stenhouse
  128623. stephan
  128624. stephane
  128625. stephen
  128626. stephenson
  128627. steppan
  128628. stepping
  128629. steps
  128630. stepwise
  128631. stepwise
  128632. electrophilic
  128633. addition
  128634. novel
  128635. synthetic
  128636. ramific
  128637. stercochemistry
  128638. stereisomerization
  128639. stereo
  128640. stereo
  128641. regiochemical
  128642. aspects
  128643. mitsunobu
  128644. reaction
  128645. regiochemistry
  128646. claisen
  128647. rearrangement
  128648. stereo
  128649. regiochemistry
  128650. claisen
  128651. rearrangement
  128652. appli
  128653. stereo
  128654. regiocontrol
  128655. complex
  128656. induced
  128657. proximity
  128658. effects
  128659. stereo
  128660. regioselective
  128661. metal
  128662. catalyzed
  128663. alkynylation
  128664. stereo-differentiati
  128665. stereo-differentiati
  128666. reactions
  128667. nature
  128668. asymmetric
  128669. stereo-electronic
  128670. stereoanalysis
  128671. stereocenters
  128672. stereocentres
  128673. stereochem
  128674. stereochemical
  128675. ochemical
  128676. dichotomies
  128677. olefin-forming
  128678. stereochemical
  128679. synthetic
  128680. studies
  128681. intramolecular
  128682. stereochemical
  128683. aspects
  128684. bisquinolizidine
  128685. alkaloids
  128686. spartei
  128687. stereochemical
  128688. aspects
  128689. radical
  128690. reactions
  128691. stereochemical
  128692. aspects
  128693. tellurium
  128694. complexes
  128695. sulfur
  128696. stereochemical
  128697. aspects
  128698. formation
  128699. chiral
  128700. allenes
  128701. stereochemical
  128702. aspects
  128703. intramoleular
  128704. diels-alder
  128705. stereochemical
  128706. aspects
  128707. synthesis
  128708. 12-epoxides
  128709. stereochemical
  128710. control
  128711. metal
  128712. catalyzed
  128713. cycloadditions
  128714. stereochemical
  128715. control
  128716. synthesis
  128717. acyclic
  128718. systems
  128719. appli
  128720. stereochemical
  128721. control
  128722. transition-metal
  128723. complexes
  128724. stereochemical
  128725. course
  128726. tungsten-promoted
  128727. cyclocarbonylatio
  128728. stereochemical
  128729. course
  128730. anionic
  128731. ylide
  128732. rearrangements
  128733. stereochemical
  128734. features
  128735. vinylic
  128736. radical
  128737. processes
  128738. stereochemical
  128739. investigation
  128740. dipolar
  128741. cycloaddition
  128742. stereochemical
  128743. studies
  128744. addition
  128745. allylstannanes
  128746. stereochemically
  128747. stereochemistry
  128748. ochemistry
  128749. catalysis
  128750. zirconium
  128751. complexes
  128752. stereochemistry
  128753. mechanism
  128754. wittig
  128755. reaction
  128756. stereochemistry
  128757. mechanism
  128758. allylic
  128759. aldehyde
  128760. conden
  128761. stereochemistry
  128762. mechanism
  128763. ketone
  128764. reductions
  128765. hydrid
  128766. stereochemistry
  128767. silicon
  128768. stereochemistry
  128769. carbenoid
  128770. formation
  128771. bromine
  128772. lithium
  128773. stereochemistry
  128774. sigmatropic
  128775. rearrangements
  128776. stereochemistry
  128777. allyl
  128778. sulfone
  128779. carbanion
  128780. alkylation
  128781. stereochemistry
  128782. allylation
  128783. phenylsulfinylethyl
  128784. stereochemistry
  128785. arenetricarbonylchro
  128786. complexes
  128787. useful
  128788. stereochemistry
  128789. catalyzed
  128790. addition
  128791. thiophenol
  128792. stereochemistry
  128793. cyclopropane
  128794. cleavage
  128795. electrophiles
  128796. stereochemistry
  128797. heterocyclic
  128798. compounds
  128799. stereochemistry
  128800. intramolecular
  128801. free-radical
  128802. cyclization
  128803. stereochemistry
  128804. metabolic
  128805. reactions
  128806. amino
  128807. acids
  128808. stereochemistry
  128809. organic
  128810. compounds
  128811. stereochemistry
  128812. organometallic
  128813. compound
  128814. addition
  128815. keton
  128816. stereochemistry
  128817. radical
  128818. cyclizations
  128819. chain
  128820. olefin
  128821. stereochemistry
  128822. addition
  128823. product
  128824. aminosuccinimid
  128825. stereochemistry
  128826. base-promoted
  128827. michael
  128828. addition
  128829. reacti
  128830. stereochemistry
  128831. reactions
  128832. transition
  128833. metal-carbon
  128834. stereochemistry
  128835. thermolytic
  128836. catalysed
  128837. decarboxylatio
  128838. stereocomplementary
  128839. stereocomplementary
  128840. construction
  128841. ethynyl
  128842. hydroxytetra
  128843. stereocontolled
  128844. stereocontrol
  128845. cycloaddition
  128846. aldimine
  128847. deriv
  128848. stereocontrol
  128849. radical
  128850. cyclizations
  128851. sugar
  128852. templates
  128853. stereocontrol
  128854. dipolar
  128855. cycloaddition
  128856. reaction
  128857. stereocontrol
  128858. synthesis
  128859. acyclic
  128860. systems
  128861. applicatio
  128862. stereocontroled
  128863. stereocontrolled
  128864. stereocontrolled
  128865. 5-exo-trig
  128866. cyclization
  128867. imidoyl
  128868. radicals
  128869. stereocontrolled
  128870. catalytic
  128871. asymmetric
  128872. reduction
  128873. ketones
  128874. stereocontrolled
  128875. construction
  128876. complex
  128877. cyclic
  128878. ketones
  128879. stereocontrolled
  128880. convergent
  128881. total
  128882. synthesis
  128883. furaquinocin
  128884. ontrolled
  128885. double
  128886. expansion
  128887. fused
  128888. allylidenecy
  128889. stereocontrolled
  128890. elaboration
  128891. quaternary
  128892. carbon
  128893. centers
  128894. stereocontrolled
  128895. nucleophilic
  128896. additions
  128897. b-bis
  128898. methoxyme
  128899. stereocontrolled
  128900. syntheses
  128901. p-chiral
  128902. analogues
  128903. nucleosi
  128904. stereocontrolled
  128905. synthesis
  128906. 3-acyl-4-alkoxy-5-ar
  128907. pentatr
  128908. stereocontrolled
  128909. synthesis
  128910. c-glycosides
  128911. stereocontrolled
  128912. synthesis
  128913. hapalindole
  128914. stereocontrolled
  128915. synthesis
  128916. isocomene
  128917. novel
  128918. photocycl
  128919. stereocontrolled
  128920. synthesis
  128921. oligo
  128922. nucleoside
  128923. phosphorothio
  128924. stereocontrolled
  128925. synthesis
  128926. chiral
  128927. aziridines
  128928. stereocontrolled
  128929. total
  128930. synthesis
  128931. paraherquamide
  128932. stereoconvergent
  128933. stereoconvergent
  128934. tandem
  128935. wittig
  128936. anionic
  128937. stereodefined
  128938. stereodefined
  128939. substituted
  128940. cyclopropyl
  128941. reagents
  128942. stereodifferentiatin
  128943. stereodifferentiatio
  128944. stereodifferentintin
  128945. stereodirected
  128946. stereodivergent
  128947. stereodivergent
  128948. additions
  128949. allylic
  128950. chromium
  128951. reagents
  128952. stereodynamics
  128953. stereoel
  128954. stereoelectric
  128955. stereoelectronic
  128956. stereoelectronic
  128957. control
  128958. reactions
  128959. ketones
  128960. stereoelectronic
  128961. effects
  128962. carboxyl
  128963. oxygen
  128964. stereoelectronic
  128965. effects
  128966. silicon
  128967. phosphorus
  128968. sulfur
  128969. stereoelectronic
  128970. effects
  128971. formatio
  128972. 6-membered
  128973. stereoelectronic
  128974. effects
  128975. formation
  128976. membere
  128977. stereoelectronic
  128978. effects
  128979. formation
  128980. stereoelectronic
  128981. effects
  128982. cetal
  128983. hydrolysis
  128984. stereoelectronic
  128985. origin
  128986. intrinsic
  128987. barrier
  128988. stereoelectronic
  128989. rules
  128990. addition
  128991. reactions
  128992. stereoelectronic
  128993. rules
  128994. addition
  128995. reactions
  128996. cram's
  128997. stereoface
  128998. stereoface
  128999. differentiation
  129000. asymmetric
  129001. synthesis
  129002. using
  129003. stereogenic
  129004. stereogenicity
  129005. stereoigomers
  129006. stereoisomeric
  129007. stereoisomerism
  129008. stereoisomers
  129009. stereolabile
  129010. stereorationale
  129011. stereoregular
  129012. stereoregulated
  129013. stereos
  129014. stereosclective
  129015. stereoseiective
  129016. stereoselection
  129017. stereoselection
  129018. chromium
  129019. mediated
  129020. intramolecular
  129021. stereoselectiveD
  129022. stereoelectronic
  129023. effects
  129024. formation
  129025. membere@
  129026. stereoinformation@
  129027. stereoselective
  129028. stereoselective
  129029. addition
  129030. cf3sime3
  129031. azirines
  129032. synthesis
  129033. stereoselective
  129034. approaches
  129035. bioactive
  129036. carbohydrates
  129037. stereoselective
  129038. construction
  129039. tetrahydrofuran
  129040. stereoselective
  129041. preparation
  129042. tetracycle
  129043. aspido@
  129044. stereoselective
  129045. synthesis
  129046. alkenes
  129047. using
  129048. unimolecular
  129049. stereoselective
  129050. synthesis
  129051. lactones
  129052. containing
  129053. alkox@
  129054. stereoselective
  129055. synthesis
  129056. retro-isomers
  129057. n-glucoaspargi@
  129058. part@
  129059. stokes@
  129060. strategies
  129061. strauss
  129062. structural
  129063. structure
  129064. structure
  129065. reactivity
  129066. cycloimmonium
  129067. ylides@
  129068. structure
  129069. small
  129070. large
  129071. rings@
  129072. strunin
  129073. studies
  129074. studies
  129075. directed
  129076. cyclopropanation
  129077. a-allenic
  129078. alcoho@
  129079. studies
  129080. intramolecular
  129081. cycloaddition
  129082. reaction
  129083. meso@
  129084. stuhl
  129085. stereoselective
  129086. stereoselective
  129087. oselective
  129088. addition
  129089. cf3sime3
  129090. azirines
  129091. synthesis
  129092. stereoselective
  129093. addition
  129094. organocopper
  129095. reagents
  129096. cyclic
  129097. stereoselective
  129098. addition
  129099. triphenylsilyl
  129100. magnesium
  129101. bromide
  129102. stereoselective
  129103. addition
  129104. reaction
  129105. organolithium
  129106. reagents
  129107. stereoselective
  129108. additions
  129109. chiral
  129110. functionalized
  129111. organozin
  129112. stereoselective
  129113. additions
  129114. nucleophilic
  129115. alkenes
  129116. chiral
  129117. stereoselective
  129118. aldol
  129119. condensations
  129120. stereoselective
  129121. alkylation
  129122. methyl
  129123. tributylstannyl
  129124. tetra
  129125. stereoselective
  129126. alkylation
  129127. reactions
  129128. chiral
  129129. metal
  129130. enolate
  129131. stereoselective
  129132. annulations
  129133. palladium
  129134. catalyzed
  129135. reaction
  129136. stereoselective
  129137. annulations
  129138. palladium-catalyzed
  129139. reaction
  129140. stereoselective
  129141. construction
  129142. tetrahydrofuran
  129143. stereoselective
  129144. construction
  129145. complete
  129146. ingenane
  129147. stereoselective
  129148. control
  129149. dipolar
  129150. cycloaddition
  129151. nitro
  129152. stereoselective
  129153. cyclization
  129154. mediated
  129155. samarium
  129156. iodide
  129157. stereoselective
  129158. cyclization
  129159. zirconocene
  129160. catalyzed
  129161. intram
  129162. stereoselective
  129163. dioxygenation
  129164. allylstannanes
  129165. synthesis
  129166. stereoselective
  129167. glycolization
  129168. allylic
  129169. alcohols
  129170. osmium
  129171. stereoselective
  129172. hydride
  129173. reductions
  129174. chiral
  129175. tolylsulfin
  129176. stereoselective
  129177. hydrogen
  129178. transfer
  129179. reactions
  129180. involving
  129181. acycli
  129182. stereoselective
  129183. hydrogen
  129184. transfer
  129185. acyclic
  129186. radicals
  129187. tetrah
  129188. stereoselective
  129189. intramolecular
  129190. bis-silyation
  129191. alkenes
  129192. stereoselective
  129193. manipulation
  129194. acetals
  129195. derived
  129196. stereoselective
  129197. organometallic
  129198. reactions
  129199. force
  129200. field
  129201. study
  129202. stereoselective
  129203. photocycloaddition
  129204. silyl
  129205. ethers
  129206. stereoselective
  129207. preparation
  129208. tetracycle
  129209. aspido
  129210. stereoselective
  129211. preparation
  129212. trifluoromethylated
  129213. organic
  129214. stereoselective
  129215. radical
  129216. cyclization
  129217. epoxy
  129218. silyl
  129219. stereoselective
  129220. reactions
  129221. alpha-carbon
  129222. organo
  129223. stereoselective
  129224. reactions
  129225. mediated
  129226. functionalized
  129227. diorgan
  129228. stereoselective
  129229. reactions
  129230. imide
  129231. substituted
  129232. radicals
  129233. stereoselective
  129234. routes
  129235. toward
  129236. synthesis
  129237. unusual
  129238. amino
  129239. stereoselective
  129240. additions
  129241. enantioenriched
  129242. allylic
  129243. stereoselective
  129244. syntheses
  129245. building-blocks
  129246. consecut
  129247. stereoselective
  129248. syntheses
  129249. carbohydrate
  129250. radicals
  129251. stereoselective
  129252. synthesis
  129253. organic
  129254. chemistry
  129255. stereoselective
  129256. synthesis
  129257. 12-trans-ribofuranos
  129258. 1-hyd
  129259. stereoselective
  129260. synthesis
  129261. disubstituted
  129262. piperidine
  129263. stereoselective
  129264. synthesis
  129265. dihydrofuranones
  129266. additi
  129267. stereoselective
  129268. synthesis
  129269. diamino
  129270. nitriles
  129271. amino
  129272. stereoselective
  129273. synthesis
  129274. lactones
  129275. containing
  129276. alkox
  129277. stereoselective
  129278. synthesis
  129279. b-mannopyranosides
  129280. stereoselective
  129281. synthesis
  129282. diastereomeric
  129283. amino
  129284. alcohols
  129285. stereoselective
  129286. synthesis
  129287. differentially
  129288. protected
  129289. deriva
  129290. stereoselective
  129291. synthesis
  129292. enantiomerically
  129293. natural
  129294. stereoselective
  129295. synthesis
  129296. erythro
  129297. a-amino
  129298. epoxides
  129299. stereoselective
  129300. synthesis
  129301. fused
  129302. lactams
  129303. intramolecul
  129304. stereoselective
  129305. synthesis
  129306. highly
  129307. substituted
  129308. lactones
  129309. stereoselective
  129310. synthesis
  129311. hydroxyethylene
  129312. dipeptide
  129313. isost
  129314. stereoselective
  129315. synthesis
  129316. chain
  129317. polyols
  129318. sequentia
  129319. stereoselective
  129320. synthesis
  129321. oxazolidinones
  129322. tandem
  129323. cycli
  129324. stereoselective
  129325. synthesis
  129326. polyfunctional
  129327. trisubsti
  129328. stereoselective
  129329. synthesis
  129330. protected
  129331. amino
  129332. alkyl
  129333. epoxides
  129334. tereoselective
  129335. synthesis
  129336. tetrahydrofurans
  129337. tetrahydro
  129338. stereoselective
  129339. synthesis
  129340. tetrahydrofurans
  129341. lewis
  129342. stereoselective
  129343. synthesis
  129344. bis-tetrahyrrofuran
  129345. fragmen
  129346. stereoselective
  129347. synthesis
  129348. trans-45-disubstitut
  129349. 13-imidazo
  129350. ective
  129351. synthesis
  129352. zirconium
  129353. complexe
  129354. stereoselective
  129355. total
  129356. syntheses
  129357. desoxoprosopinine
  129358. stereoselective
  129359. transformations
  129360. mediated
  129361. chiral
  129362. monocyclo
  129363. stereoselective
  129364. ynthesis
  129365. stereoselectivites
  129366. stereoselectivities
  129367. stereoselectivity
  129368. stereoselectivity
  129369. during
  129370. cycloadditions
  129371. leading
  129372. functiona
  129373. stereoselectivity
  129374. intramolecular
  129375. diene
  129376. cycloaromatization
  129377. stereoselectivity
  129378. reactions
  129379. 12-dioxy-substituted
  129380. radic
  129381. stereoselectivity
  129382. reactions
  129383. bicyclo
  129384. 3.3.0
  129385. stereoselectivity
  129386. diels
  129387. alder
  129388. reaction
  129389. effect
  129390. stereoselectivity
  129391. peterson
  129392. reaction
  129393. application
  129394. stereoselectivity
  129395. wittig
  129396. reaction
  129397. aromatic
  129398. ketones
  129399. stereoselectivity
  129400. 13-dipolar
  129401. cycloaddition
  129402. glycosyl
  129403. stereoselectivity
  129404. intramolecular
  129405. cyclisations
  129406. nitrones
  129407. stereoselectivity
  129408. transfer
  129409. hydrogen
  129410. atoms
  129411. cycli
  129412. stereospecific}
  129413. stereospecific
  129414. a-alkoxystannane
  129415. couplings
  129416. chloride
  129417. stereospecific
  129418. annulation
  129419. sequential
  129420. opening
  129421. stereospecific
  129422. cyclic
  129423. ketone
  129424. formation
  129425. anatomy
  129426. stereospecific
  129427. dehydrative
  129428. alkylation
  129429. sulfones
  129430. stereospecific
  129431. dehydrative
  129432. alkylation
  129433. sulfones
  129434. reduct
  129435. stereospecific
  129436. dehydrative
  129437. alkylation
  129438. bis-sulfones
  129439. synthe
  129440. stereospecific
  129441. deoxygenation
  129442. epoxides
  129443. olefins
  129444. stereospecific
  129445. insertion
  129446. carbene
  129447. ligand
  129448. fisher
  129449. stereospecific
  129450. intramolecular
  129451. diels
  129452. alder
  129453. reaction
  129454. stereospecific
  129455. palladium
  129456. copper
  129457. cocatalyzed
  129458. cross
  129459. coupling
  129460. stereospecific
  129461. palladium/copper
  129462. cocatalyzed
  129463. cross-coupling
  129464. stereospecific
  129465. preparation
  129466. reactivity
  129467. utility
  129468. polyflu
  129469. stereospecific
  129470. reaction
  129471. nitrilium
  129472. analogous
  129473. stereospecific
  129474. reduction
  129475. nitrile
  129476. formation
  129477. stereospecific
  129478. synthesis
  129479. olefins
  129480. through
  129481. sequential
  129482. cross
  129483. stereospecific
  129484. synthesis
  129485. temarotene
  129486. structural
  129487. isomer
  129488. stereospecific
  129489. telluride
  129490. mediated
  129491. conversion
  129492. epoxides
  129493. stereospecificity
  129494. stereospecificity
  129495. enzymology
  129496. place
  129497. evolution
  129498. stereostructural
  129499. stereostructure
  129500. stereotriads
  129501. steric
  129502. steric
  129503. steric
  129504. control
  129505. based
  129506. alkyl
  129507. substituents
  129508. sigmatr
  129509. steric
  129510. course
  129511. mechanism
  129512. 13-dipolar
  129513. cycloadditions
  129514. steric
  129515. course
  129516. kinetic
  129517. 12-addition
  129518. anions
  129519. conjug
  129520. steric
  129521. effect
  129522. trifluoromethyl
  129523. group
  129524. based
  129525. result
  129526. steric
  129527. effects
  129528. phosphorus
  129529. ligands
  129530. organometallic
  129531. chemi
  129532. steric
  129533. influence
  129534. trimethyl
  129535. silyl
  129536. group
  129537. organic
  129538. steric
  129539. influence
  129540. trimethyl
  129541. silyl
  129542. group
  129543. inorganic
  129544. steric
  129545. influence
  129546. trimethylsilyl
  129547. group
  129548. organic
  129549. steric
  129550. interaction
  129551. organic
  129552. chemistry
  129553. spatial
  129554. requirements
  129555. steric
  129556. interactions
  129557. double
  129558. bonds
  129559. sterically
  129560. sterically
  129561. crowded
  129562. organic
  129563. molecules
  129564. synthesis
  129565. structure
  129566. stern
  129567. sternbach
  129568. sternberg
  129569. sternson
  129570. steroid
  129571. steroid
  129572. reactions
  129573. partial
  129574. synthesis
  129575. steroid
  129576. total
  129577. synthesis
  129578. steroidal
  129579. steroidal
  129580. oligoglycosides
  129581. polyhydroxysteroids
  129582. echin
  129583. steroidsY
  129584. steroids
  129585. asstructural
  129586. components
  129587. molecular
  129588. engineering
  129589. steroids
  129590. reactions
  129591. partial
  129592. syntheses
  129593. steroids
  129594. chain
  129595. containing
  129596. heterocyclic
  129597. fragmen
  129598. sterol
  129599. stetter
  129600. stetter
  129601. hermann
  129602. kuhlmann
  129603. heinrich
  129604. catalyzed
  129605. nucleophilic
  129606. stevan
  129607. steve
  129608. steven
  129609. stevens
  129610. stevens
  129611. stevenson
  129612. stevioside
  129613. stevioside
  129614. related
  129615. sweet
  129616. diterpenoid
  129617. glycosides
  129618. stewart
  129619. stewart
  129620. benkovic
  129621. stephen
  129622. catalytic
  129623. antibodies
  129624. mechan
  129625. stewart
  129626. srinivasan
  129627. proton
  129628. activating
  129629. factors
  129630. general
  129631. steyn
  129632. steyn
  129633. biosynthesis
  129634. mycotoxins
  129635. academic
  129636. press
  129637. steynberg
  129638. stibabenzene
  129639. stibides
  129640. stibine
  129641. stibonium
  129642. stibr
  129643. stibr
  129644. bohumil
  129645. carboranes
  129646. other
  129647. c2biohl2
  129648. stick
  129649. stidsen
  129650. stief
  129651. stiff
  129652. stigmasterol
  129653. stilbene
  129654. stilbene-amine
  129655. stilbenes
  129656. stilbenes
  129657. potential
  129658. biological
  129659. activity
  129660. still
  129661. stille
  129662. stille
  129663. coupling
  129664. reaction
  129665. using
  129666. trimethylsilyl
  129667. 2-butenylsta
  129668. stimczyk
  129669. stimulant
  129670. stirling
  129671. stirling
  129672. chemistry
  129673. sulphonium
  129674. group
  129675. stirling
  129676. evaluation
  129677. strain
  129678. effects
  129679. reactivit
  129680. stirling
  129681. leaving
  129682. groups
  129683. nucleofugality
  129684. eliminat
  129685. stirling
  129686. nucleophilic
  129687. eliminative
  129688. fission
  129689. stitution
  129690. stmcture
  129691. stobbe
  129692. stock
  129693. stock
  129694. wasielewski
  129695. charge
  129696. delocalization
  129697. stock
  129698. wasielewski
  129699. trifluoromethyl
  129700. group
  129701. chemi
  129702. stoddard
  129703. stoddart
  129704. stoddart
  129705. fraser
  129706. making
  129707. molecules
  129708. order
  129709. chemistry
  129710. brita
  129711. stoddart
  129712. fraser
  129713. cyclodextrins
  129714. shelf
  129715. components
  129716. stoeva
  129717. stoianova
  129718. stoianova
  129719. ivanova
  129720. composition
  129721. bulgarian
  129722. flower
  129723. stoichiometric
  129724. stoichiometric
  129725. applications
  129726. organotransition
  129727. metal
  129728. comple
  129729. stoichiometric
  129730. reactions
  129731. organo-pi-metal
  129732. complexes
  129733. stokes
  129734. stoll
  129735. stoller
  129736. stoltefuss
  129737. stolyarov
  129738. stolze
  129739. stone
  129740. stone
  129741. gordon
  129742. leaving
  129743. stone
  129744. unturned
  129745. pathways
  129746. organ
  129747. stone
  129748. pressure
  129749. spectrometric
  129750. studies
  129751. silico
  129752. stone
  129753. stabilization
  129754. carbenium
  129755. silicon
  129756. stones
  129757. stoodley
  129758. stoodley
  129759. thiazines
  129760. their
  129761. dihydro
  129762. derivatives
  129763. stool
  129764. stopped
  129765. storage
  129766. storck
  129767. stores
  129768. stork
  129769. stork
  129770. gilbert
  129771. hutchinson
  129772. okabe
  129773. parker
  129774. choon
  129775. story
  129776. stoss
  129777. stoss
  129778. peter
  129779. hemmer
  129780. reinhard
  129781. 14:36
  129782. dianhydro
  129783. hexitols
  129784. stothers
  129785. stott
  129786. stout
  129787. stowell
  129788. stowell
  129789. neoglycoproteins
  129790. preparation
  129791. stowell
  129792. carbanions
  129793. organic
  129794. synthesis
  129795. wiley
  129796. interscien
  129797. stowell
  129798. intermediate
  129799. organic
  129800. chemistry
  129801. wiley
  129802. stpanov
  129803. strachan
  129804. strack
  129805. straight
  129806. straightforward
  129807. strain
  129808. strain
  129809. assisted
  129810. syntheses
  129811. strain
  129812. effects
  129813. amine
  129814. basicity
  129815. strained
  129816. bridgehead
  129817. alcohols
  129818. derivatives
  129819. strained
  129820. bridgehead
  129821. double
  129822. bonds
  129823. strained
  129824. bridgehead
  129825. double
  129826. bonds
  129827. strain
  129828. bredt
  129829. strained
  129830. cyclic
  129831. cumulenes
  129832. strained
  129833. olefins
  129834. structure
  129835. reactivity
  129836. nonplanar
  129837. carbo
  129838. strained
  129839. organic
  129840. molecules
  129841. strained
  129842. policyclic
  129843. systems
  129844. effect
  129845. strain
  129846. chemical
  129847. stranded
  129848. stransky
  129849. strategiesx
  129850. strategies
  129851. synthesis
  129852. prostacyclins
  129853. strategies
  129854. liquid
  129855. chromatographic
  129856. resolution
  129857. enantiom
  129858. strategies
  129859. macrolide
  129860. synthesis
  129861. concise
  129862. approach
  129863. strategies
  129864. synthesis
  129865. heterocyclic
  129866. natural
  129867. product
  129868. strategies
  129869. optical
  129870. resolutions
  129871. strategy
  129872. strauss
  129873. strauss
  129874. strauss
  129875. steven
  129876. search
  129877. larger
  129878. weakly
  129879. coord
  129880. strazewski
  129881. strazzolini
  129882. streit
  129883. streith
  129884. streitwieser
  129885. streitwieser
  129886. juaristie
  129887. nebenzahl
  129888. equilibrium
  129889. strekova
  129890. strekowski
  129891. strekowski
  129892. lucjan
  129893. molecular
  129894. basis
  129895. enhancement
  129896. strength
  129897. streptonigrin
  129898. streptonigrone
  129899. stretch
  129900. strings
  129901. stripping
  129902. strittmatter
  129903. strobilurins
  129904. strohl
  129905. strokin
  129906. stroll
  129907. strominger
  129908. strong
  129909. strontium
  129910. strouf
  129911. struchkov
  129912. structurai
  129913. structuralO
  129914. structural
  129915. structural
  129916. characterization
  129917. calicheamicin-dna
  129918. complex
  129919. structural
  129920. characterization
  129921. organocopper
  129922. complexes
  129923. structural
  129924. characterization
  129925. organocuprate
  129926. reagents
  129927. exafs
  129928. consequences
  129929. bonding
  129930. transition
  129931. metal
  129932. carbe
  129933. structural
  129934. elucidation
  129935. chiral
  129936. syntheses
  129937. insect
  129938. pherom
  129939. structural
  129940. features
  129941. reactivity
  129942. tetrahalomethanes
  129943. structural
  129944. mechanistic
  129945. theoretical
  129946. aspects
  129947. chelation-
  129948. structural
  129949. prope
  129950. organocobalt
  129951. coenzyme
  129952. models
  129953. structural
  129954. relationships
  129955. silatrane
  129956. molecules
  129957. structurally
  129958. structurally
  129959. characterized
  129960. organometallic
  129961. hydroxo
  129962. complexes
  129963. structure
  129964. structure
  129965. structure
  129966. biosynthesis
  129967. cyclopropane-contain
  129968. sterols
  129969. structure
  129970. bonding
  129971. compounds
  129972. structure
  129973. dynamics
  129974. phosphorus
  129975. stabilized
  129976. carbanions
  129977. structure
  129978. reactivities
  129979. pentacoordinate
  129980. organosilicon
  129981. structure
  129982. reactivity
  129983. organometallic
  129984. chemistry
  129985. structure
  129986. reactivity
  129987. alkali
  129988. metal
  129989. enolates
  129990. structure
  129991. reactivity
  129992. carbenes
  129993. having
  129994. substituent
  129995. structure
  129996. reactivity
  129997. cycloimmonium
  129998. ylides
  129999. structure
  130000. reactivity
  130001. cyclopropanones
  130002. triaful
  130003. structure
  130004. reactivity
  130005. halosulfonium
  130006. salts
  130007. structure
  130008. reactivity
  130009. halosulphonium
  130010. salts
  130011. structure
  130012. reactivity
  130013. enolates
  130014. pinacolone
  130015. structure
  130016. reactivity
  130017. organic
  130018. radical
  130019. cations
  130020. structure
  130021. reactivity
  130022. radical
  130023. structure
  130024. stereochemistry
  130025. transition
  130026. states
  130027. structure
  130028. determination
  130029. analyses
  130030. organosilicon
  130031. compou
  130032. structure
  130033. dynamics
  130034. electronic
  130035. properties
  130036. cobaltocene
  130037. structure
  130038. benzylpotassium
  130039. benzylrubidium
  130040. structure
  130041. five-membered
  130042. rings
  130043. heteroatom
  130044. structure
  130045. five-membered
  130046. rings
  130047. heteroatom
  130048. structure
  130049. lithium
  130050. hexamethyldisilazide
  130051. spectroscopic
  130052. structure
  130053. hydrocarbon
  130054. solution
  130055. assignmen
  130056. structure
  130057. six-membered
  130058. rings
  130059. structure
  130060. small
  130061. large
  130062. rings
  130063. structure-activity
  130064. structure-behavior
  130065. structure-behavior
  130066. relationship
  130067. enantiosele
  130068. structure-directed
  130069. structure-effectivit
  130070. structure-stereochem
  130071. structuresL
  130072. structures
  130073. carbenes
  130074. stereochemistry
  130075. carbene
  130076. structures
  130077. lithium
  130078. enolates
  130079. phenolates
  130080. solution
  130081. structures
  130082. intermediate
  130083. complexes
  130084. friedel-crafts
  130085. structuring
  130086. strukul
  130087. strukul
  130088. georgio
  130089. catalytic
  130090. oxidations
  130091. hydrogen
  130092. peroxi
  130093. strunin
  130094. strunin
  130095. strunin
  130096. chemical
  130097. transformations
  130098. aminoglycoside
  130099. antib
  130100. struve
  130101. strychnine
  130102. strychnos
  130103. stuart
  130104. stubenrauch
  130105. stuchkov
  130106. studabaker
  130107. student's
  130108. studied
  130109. studiesV
  130110. studies
  130111. studies
  130112. directed
  130113. synthesis
  130114. unusual
  130115. cardiotoxic
  130116. studies
  130117. molecular
  130118. recognition
  130119. studies
  130120. porphyrin
  130121. chemistry
  130122. synthetic
  130123. approach
  130124. invited
  130125. studies
  130126. sesquiterpene
  130127. synthesis
  130128. quadrone
  130129. phyllanthoci
  130130. studies
  130131. directed
  130132. cyclopropanation
  130133. a-allenic
  130134. alcoho
  130135. studies
  130136. transmetalation
  130137. cyclopropyl
  130138. vinyl
  130139. studies
  130140. intramolecular
  130141. diels
  130142. alder
  130143. reactions
  130144. intro
  130145. studies
  130146. organic
  130147. oligo
  130148. polyradicals
  130149. means
  130150. studies
  130151. chromone
  130152. derivatives
  130153. regioselective
  130154. dipolar
  130155. studies
  130156. claisen
  130157. rearrangement
  130158. substituted
  130159. allyloxyin
  130160. studies
  130161. dynemicin
  130162. nonradical
  130163. cycloaromatization
  130164. pathway
  130165. studies
  130166. intramolecular
  130167. higher-order
  130168. cycloaddition
  130169. reactio
  130170. studies
  130171. isocyanides
  130172. related
  130173. compounds
  130174. novel
  130175. synthes
  130176. studies
  130177. isocyanides
  130178. related
  130179. compounds
  130180. unusual
  130181. studies
  130182. organosilicon
  130183. chemistry
  130184. reaction
  130185. oxirany
  130186. studies
  130187. oxazoline
  130188. thiazoline
  130189. oxidations
  130190. reliable
  130191. studies
  130192. alkylation
  130193. chiral
  130194. enolates
  130195. application
  130196. studies
  130197. chemistry
  130198. mitomycins
  130199. studies
  130200. enantiospecific
  130201. synthesis
  130202. oxindole
  130203. alkaloi
  130204. studies
  130205. intramolecular
  130206. cycloaddition
  130207. reaction
  130208. studies
  130209. photochemistry
  130210. taxol
  130211. studies
  130212. oxonia
  130213. rearrangement
  130214. studies
  130215. selective
  130216. acyliminium
  130217. cyclization
  130218. studies
  130219. synthesis
  130220. solenolide
  130221. mediated
  130222. studies
  130223. synthesis
  130224. strychnos
  130225. indole
  130226. alkaloids
  130227. synth
  130228. study
  130229. lithiation
  130230. substituted
  130231. carbolines
  130232. study
  130233. regioselectivity
  130234. palladium
  130235. catalyzed
  130236. monocou
  130237. study
  130238. reaction
  130239. without
  130240. medium
  130241. under
  130242. microwave
  130243. studying
  130244. studzinskii
  130245. stuhl
  130246. stuhl
  130247. stumbled
  130248. stumer
  130249. stumpf
  130250. sturgess
  130251. sturkovich
  130252. sturmer
  130253. stuttgartu
  130254. style
  130255. stypoldione
  130256. styren
  130257. styren
  130258. amine
  130259. stilbene-amine
  130260. intramolecular
  130261. addition
  130262. styrene
  130263. styrenes
  130264. styrylchromones
  130265. catalytic
  130266. codimerization
  130267. ethylene
  130268. butadiene
  130269. suami
  130270. suaveoline
  130271. subbotin
  130272. subergorgic
  130273. subfamily
  130274. subgroup
  130275. subhas
  130276. subhash
  130277. subheterocyclic
  130278. suboxide
  130279. subramanian
  130280. subsequent
  130281. quent
  130282. introduction
  130283. amino
  130284. group
  130285. peptides
  130286. subsequent
  130287. introduction
  130288. alpha-carboxy
  130289. group
  130290. peptides
  130291. substance
  130292. substances
  130293. stuhl
  130294. subsequent
  130295. introduction
  130296. amino
  130297. group
  130298. peptides@
  130299. olecular
  130300. diels-alde@
  130301. substituted
  130302. substitution
  130303. substitution
  130304. addition
  130305. reactions
  130306. thiocyanogen@
  130307. substitutive
  130308. subtypes@
  130309. sulfenyl@
  130310. sulfinylcycloalkanon
  130311. sulfonium
  130312. sulfoxides
  130313. sulfur
  130314. sulfuranyl@
  130315. summers@
  130316. superphanes@
  130317. supramolecular
  130318. surrogates
  130319. sutton
  130320. derek
  130321. organometallic
  130322. diazo
  130323. compounds
  130324. chemical
  130325. reviews@
  130326. swindell
  130327. charles
  130328. taxane
  130329. diterpene
  130330. synthesis
  130331. strategies
  130332. symmetrical@
  130333. synchronization@
  130334. synth
  130335. syntheses
  130336. syntheses
  130337. 3-amino-2-azetidinon
  130338. literature
  130339. survey
  130340. tetrah@
  130341. syntheses
  130342. first
  130343. selenium
  130344. containing
  130345. bicyclic
  130346. lactam@
  130347. synthesis
  130348. 2-alkyl-13-cyclopent
  130349. substances
  130350. substantive
  130351. substi
  130352. substituent
  130353. ituent
  130354. solvent
  130355. effects
  130356. intramolecular
  130357. diels-alde
  130358. substituent
  130359. structural
  130360. effects
  130361. ozonolysis
  130362. substituent
  130363. effects
  130364. diastereoselective
  130365. cycloaddit
  130366. substituent
  130367. effects
  130368. rearrangement
  130369. alkyl
  130370. substituent
  130371. effects
  130372. photochemical
  130373. hydrogen
  130374. abstraction
  130375. substituent
  130376. effects
  130377. strength
  130378. bonds
  130379. kinetic
  130380. substituent-free
  130381. substituents
  130382. substitut
  130383. substituted
  130384. substituted
  130385. substituted
  130386. triazolium
  130387. ylides
  130388. dipoles
  130389. synthons
  130390. substituted
  130391. 123-triazolium-1-yli
  130392. 13-dipoles
  130393. synthons
  130394. substituted
  130395. azides
  130396. selenium
  130397. promoted
  130398. deselenenylation
  130399. substituted
  130400. lithium
  130401. tosyl
  130402. propenolates
  130403. useful
  130404. intermediat
  130405. substituted
  130406. vinyl
  130407. azides
  130408. synthesis
  130409. substituted123
  130410. substitutedhex
  130411. substitutes
  130412. substitutionq
  130413. substitution
  130414. addition
  130415. reactions
  130416. thiocyanogen
  130417. substitution
  130418. addition
  130419. reactions
  130420. thiocyanogen
  130421. substitution
  130422. allylic
  130423. functional
  130424. acetates
  130425. stereoselective
  130426. substitution
  130427. reactions
  130428. using
  130429. organocopper
  130430. reagents
  130431. substitution
  130432. reactions
  130433. using
  130434. organocopper
  130435. reagents
  130436. substitution
  130437. reactions
  130438. which
  130439. radical
  130440. anion
  130441. inter
  130442. substitutions
  130443. substitutive
  130444. substitutive
  130445. substoichiometric
  130446. substrate
  130447. substrate
  130448. controlled
  130449. aldol
  130450. reaction
  130451. chiral
  130452. ethyl
  130453. ketones
  130454. substrate
  130455. controlled
  130456. group
  130457. selective
  130458. radical
  130459. cyclizations
  130460. substrate
  130461. regulation
  130462. product
  130463. distribution
  130464. reaction
  130465. substrate-directable
  130466. substrate-directable
  130467. chemical
  130468. reactions
  130469. substrate-directed
  130470. substrate-directed
  130471. synthesis
  130472. rapid
  130473. assembly
  130474. novel
  130475. substrates
  130476. subunitc
  130477. subunits
  130478. successful
  130479. successive
  130480. succinaldehyde
  130481. succinic
  130482. succinimides
  130483. succinimidoyl
  130484. suckling
  130485. sucrose
  130486. sucrose
  130487. derivatives
  130488. sucrow
  130489. sudhir
  130490. sudnev
  130491. suecica
  130492. sueros
  130493. sufur
  130494. sugar
  130495. sugars
  130496. sugars
  130497. chiral
  130498. auxiliaries
  130499. synthesis
  130500. enantiomer
  130501. sugden
  130502. suggested
  130503. suggestions
  130504. sugimoto
  130505. sugimura
  130506. suguna
  130507. suhasp
  130508. suicide
  130509. suitable
  130510. sujino
  130511. sujit
  130512. sukhbmder
  130513. sukumaran
  130514. sulfamic
  130515. sulfamide
  130516. sulfamides
  130517. sulfanes
  130518. sulfanyl
  130519. sulfate
  130520. sulfated
  130521. sulfates
  130522. sulfenamides
  130523. their
  130524. derivatives
  130525. sulfenates
  130526. sulfenes
  130527. sulfenes
  130528. their
  130529. derivatives
  130530. sulfenic
  130531. sulfenyl
  130532. sulfenylated
  130533. sulfenylating
  130534. sulfenylation
  130535. sulfide
  130536. sulfides
  130537. sulfides
  130538. organic
  130539. synthesis
  130540. applications
  130541. sulfides
  130542. sulfides
  130543. synthesis
  130544. properties
  130545. sulfilimines
  130546. sulfilr
  130547. sulfimides
  130548. sulfinate
  130549. sulfinates
  130550. sulfine
  130551. sulfine
  130552. chemistry
  130553. sulfines
  130554. sulfines
  130555. their
  130556. derivatives
  130557. sulfinic
  130558. sulfinic
  130559. acids
  130560. their
  130561. derivatives
  130562. sulfinyl
  130563. sulfinylallyl
  130564. sulfinylcycloalkanon
  130565. sulfinylcycloalkanon
  130566. sulfinylfurfural
  130567. sulfinyloxiranes
  130568. sulfites
  130569. sulfolene
  130570. sulfolenes
  130571. sulfonamide
  130572. sulfonamides
  130573. sulfonate
  130574. sulfonates
  130575. sulfonation
  130576. sulfone
  130577. sulfone
  130578. chemistry
  130579. review
  130580. sulfone
  130581. directed
  130582. alkylative
  130583. bridge
  130584. cleavage
  130585. oxabicyclic
  130586. sulfones
  130587. sulfones
  130588. their
  130589. derivatives
  130590. sulfones
  130591. organic
  130592. synthesis
  130593. sulfones
  130594. substitution
  130595. c-nucleophiles
  130596. sulfonic
  130597. sulfonic
  130598. acids
  130599. their
  130600. derivatives
  130601. sulfonium
  130602. sulfonium
  130603. sulfonium
  130604. salts
  130605. coordination
  130606. number
  130607. heteroorganosulfo
  130608. sulfonium
  130609. salts
  130610. coordination
  130611. number
  130612. sulfonyl
  130613. sulfonyl
  130614. esters
  130615. preparation
  130616. dichloromethyl
  130617. sulfones
  130618. sulfonyl
  130619. mechanisms
  130620. evidence
  130621. stereoelectronic
  130622. effect
  130623. sulfonylalkanesulfen
  130624. sulfonylamino
  130625. sulfonylaminoalkyl
  130626. sulfonylenamines
  130627. sulfonyloxaziridines
  130628. sulfonyloxiranes
  130629. sulforaphane
  130630. sulfosylic
  130631. sulfoxide
  130632. sulfoxide-stabilized
  130633. sulfoxides
  130634. sulfoxides
  130635. sulfoxides
  130636. stereochemical
  130637. control
  130638. organometallic
  130639. sulfoxides
  130640. their
  130641. derivatives
  130642. sulfoximides
  130643. sulfoximine
  130644. sulfoximines
  130645. sulfoxy
  130646. sulfoxyl
  130647. sulfoxyl
  130648. cations
  130649. sulfoxyl
  130650. derivatives
  130651. sulfur
  130652. sulfur
  130653. sulfur
  130654. analogs
  130655. polycyclic
  130656. aromatic
  130657. hydrocarbons
  130658. thiaarene
  130659. sulfur
  130660. phosphorus
  130661. peroxides
  130662. sulfur
  130663. seleno-sugar
  130664. modified
  130665. nucleosides
  130666. synthesis
  130667. chemi
  130668. sulfur
  130669. extrusion
  130670. reactions-scope
  130671. mechanistic
  130672. aspects
  130673. sulfur
  130674. stabilization
  130675. sulfur
  130676. stabilized
  130677. carbenium
  130678. salts
  130679. sulfur
  130680. ylide
  130681. vinylation
  130682. halides
  130683. mesylates
  130684. sulfur
  130685. ylide
  130686. vinylation
  130687. halides
  130688. mesylation
  130689. sulfur
  130690. ylides
  130691. sulfur-carbon
  130692. sulfur-containing
  130693. sulfur-mediated
  130694. sulfur-mediated
  130695. expansions
  130696. total
  130697. synthesis
  130698. sulfur-rich
  130699. sulfuranes
  130700. sulfuranes
  130701. organic
  130702. reactions
  130703. synthesis
  130704. sulfuranyl
  130705. sulfurated
  130706. sulfuric
  130707. sulfuric
  130708. derivatives
  130709. sulfurous
  130710. sulfuryl
  130711. sullivan
  130712. sullivan
  130713. chiral
  130714. lanthanide
  130715. shift
  130716. reagents
  130717. sulphenes
  130718. sulphenic
  130719. sulphenylating
  130720. sulphide
  130721. sulphides
  130722. sulphilimines
  130723. sulphinic
  130724. sulphinylaniline
  130725. sulphonamides
  130726. sulphones
  130727. sulphonic
  130728. sulphonium
  130729. sulphonyl
  130730. sulphonyl
  130731. transfer
  130732. reactions
  130733. sulphoxide
  130734. sulphoxides
  130735. sulphoximides
  130736. sulphur
  130737. sulphur-containing
  130738. sultam
  130739. sultams
  130740. sultana
  130741. sultanbawa
  130742. sultanbawa
  130743. xanthonoids
  130744. tropical
  130745. plants
  130746. sultone
  130747. sultone
  130748. chemistry
  130749. sults
  130750. sumiya
  130751. summary
  130752. summary
  130753. katritzky
  130754. research
  130755. group
  130756. scientific
  130757. results
  130758. summers
  130759. summers
  130760. phenanthrolines
  130761. advances
  130762. hetero
  130763. summit
  130764. sundaralingam
  130765. sundarameurthy
  130766. sundberg
  130767. sungsook
  130768. sunil
  130769. sunjic
  130770. sunko
  130771. sunlight
  130772. super
  130773. super
  130774. bases
  130775. derived
  130776. hexenyllithium
  130777. alkali
  130778. metal
  130779. super
  130780. phanes
  130781. superacid
  130782. superacids
  130783. superacids-efficient
  130784. superbases
  130785. superbases
  130786. their
  130787. organic
  130788. synthesis
  130789. superbases
  130790. powerful
  130791. tools
  130792. organic
  130793. syntheses
  130794. superbases
  130795. organic
  130796. synthesis
  130797. superbasic
  130798. superconductors
  130799. supercritical
  130800. supercritical
  130801. fluid
  130802. chromatography
  130803. micro-hplc
  130804. progress
  130805. superelectrophiles
  130806. superior
  130807. superoxide
  130808. superoxide
  130809. oxidation
  130810. reagent
  130811. superoxide
  130812. review
  130813. superphane
  130814. superphanes
  130815. supersonic
  130816. supertripodal
  130817. supinidine
  130818. suppan
  130819. supplement
  130820. supplement
  130821. chemistry
  130822. sulfur
  130823. containing
  130824. functional
  130825. supplementsW
  130826. support
  130827. supported
  130828. supported
  130829. metal
  130830. complex
  130831. catalysts
  130832. supported
  130833. reagents
  130834. preparation
  130835. analysi
  130836. applications
  130837. supported
  130838. rhodium
  130839. catalysts
  130840. aspects
  130841. formation
  130842. supports
  130843. suppots
  130844. supracyclopentadieny
  130845. suprafaciality
  130846. suprafaciality
  130847. thermal
  130848. alkenylhydroxylamine
  130849. cyclizati
  130850. suprafaciality
  130851. thermal
  130852. n-4-alkenylhydroxyla
  130853. cyclizations
  130854. supramolecul
  130855. supramolecul
  130856. metallocatalysts
  130857. cleavage
  130858. amino
  130859. supramolecular
  130860. supramolecular
  130861. supramolecular
  130862. assemblies
  130863. based
  130864. calixarenes
  130865. supramolecular
  130866. chemistry
  130867. introduction
  130868. supramolecular
  130869. control
  130870. molecular
  130871. electronic
  130872. behaviour
  130873. supramolecules
  130874. surface
  130875. surface-bound
  130876. surface-bound
  130877. metal
  130878. hydrocarbyls
  130879. organometallic
  130880. connections
  130881. surfaces
  130882. surfactant
  130883. surkov
  130884. surpateanu
  130885. surprises
  130886. surprising
  130887. surprisingly
  130888. surprisingly
  130889. diastereoselection
  130890. aldol
  130891. reactions
  130892. surrel
  130893. surrogate
  130894. surrogates
  130895. surrogates
  130896. surrounded
  130897. survey
  130898. surveys
  130899. survival
  130900. surya
  130901. surzur
  130902. susan
  130903. suschitzky
  130904. suska
  130905. suska
  130906. alina
  130907. grajkowski
  130908. andrzej
  130909. andrzej
  130910. uznanski
  130911. bogdan
  130912. suspension
  130913. georg
  130914. cooperative
  130915. effect
  130916. complexes
  130917. sustman
  130918. sustmann
  130919. susumu
  130920. sutbeyaz
  130921. suter
  130922. sutherland
  130923. sutherland
  130924. initiation
  130925. cyclization
  130926. using
  130927. methylc
  130928. sutton
  130929. sutton
  130930. derek
  130931. organometallic
  130932. diazo
  130933. compounds
  130934. chemical
  130935. reviews
  130936. suzuki
  130937. suzuki
  130938. akira
  130939. synthetic
  130940. transformations
  130941. organoboron
  130942. suzuki
  130943. novel
  130944. lewis
  130945. catalysis
  130946. organic
  130947. synthesis
  130948. suzuki
  130949. total
  130950. synthesis
  130951. glycoside
  130952. antibiotics
  130953. suzukib
  130954. sveda
  130955. svendsen
  130956. sviridov
  130957. svistunova
  130958. svoboda
  130959. svoronos
  130960. swainsonine
  130961. swartling
  130962. swarts
  130963. sweeney
  130964. sweeney
  130965. joseph
  130966. alcohols
  130967. phenols
  130968. ethers
  130969. contemporary
  130970. sweeny
  130971. sweet
  130972. sweetening
  130973. sweigart
  130974. swenton
  130975. swern
  130976. swierczewski
  130977. swinbourne
  130978. swinbourne
  130979. klinkert
  130980. advances
  130981. indolizine
  130982. swincer
  130983. swindell
  130984. swindell
  130985. charles
  130986. taxane
  130987. diterpene
  130988. synthesis
  130989. strategies
  130990. swindell
  130991. charles
  130992. taxane
  130993. diterpene
  130994. synthesis
  130995. strategies
  130996. swingle
  130997. swinholide
  130998. switches
  130999. switching
  131000. switzerland
  131001. sydia
  131002. sydney
  131003. sydnone
  131004. sydnones
  131005. syhthesis
  131006. sykes
  131007. sylvie
  131008. symmetric
  131009. symmetry
  131010. symmetry-driven
  131011. symmetry-driven
  131012. synthesis
  131013. indole
  131014. alkaloids
  131015. asymmetric
  131016. symposia
  131017. symposium
  131018. syn-3
  131019. syn-b
  131020. synaptosome
  131021. synchronization
  131022. synchronous
  131023. synergism
  131024. synlettx
  131025. synlett
  131026. overview
  131027. total
  131028. synthesis
  131029. pyrroli
  131030. synlett
  131031. metal
  131032. carbene
  131033. synthon
  131034. introduc
  131035. synposium
  131036. applications
  131037. phosphoryl-stabilise
  131038. anions
  131039. synth
  131040. synth
  131041. synthase
  131042. synthe
  131043. synthe
  131044. quinones
  131045. syntheis
  131046. synthes
  131047. synthes
  131048. reactivity
  131049. tricarbonyl
  131050. complexes
  131051. syntheses|
  131052. syntheses
  131053. syntheses
  131054. chemical
  131055. behaviors
  131056. persistent
  131057. thioaminyl
  131058. syntheses
  131059. molecular
  131060. structures
  131061. organolanthanoids
  131062. syntheses
  131063. reactions
  131064. alkyl
  131065. cyclopentanediones
  131066. syntheses
  131067. reactions
  131068. arsenides
  131069. stibides
  131070. bismuthides
  131071. syntheses
  131072. reactions
  131073. fluoroorganic
  131074. acyclic
  131075. thiocarbeni
  131076. syntheses
  131077. reactions
  131078. polyelementorganic
  131079. compo
  131080. syntheses
  131081. separations
  131082. using
  131083. functional
  131084. polymers
  131085. syntheses
  131086. 3-amino-2-azetidinon
  131087. literature
  131088. survey
  131089. tetrah
  131090. syntheses
  131091. aliphatic
  131092. azacrown
  131093. compounds
  131094. syntheses
  131095. cyclic
  131096. ureas
  131097. alpha-ureidoalkylati
  131098. syntheses
  131099. deoxy
  131100. oligosaccharides
  131101. syntheses
  131102. enantiomerically
  131103. compound
  131104. syntheses
  131105. syntheses
  131106. heterocycles
  131107. intramolecular
  131108. cyclization
  131109. syntheses
  131110. heterocycles
  131111. alkylidenephosphor
  131112. syntheses
  131113. heterocyclic
  131114. compounds
  131115. involving
  131116. aromatic
  131117. lithi
  131118. syntheses
  131119. indolizidine
  131120. alkaloids
  131121. review
  131122. 1979-1985
  131123. syntheses
  131124. medium
  131125. sized
  131126. rings
  131127. expansion
  131128. reactions
  131129. syntheses
  131130. novel
  131131. bicyclic
  131132. lactams
  131133. intramolecular
  131134. syntheses
  131135. organic
  131136. compounds
  131137. presence
  131138. fused
  131139. syntheses
  131140. polycyclic
  131141. natural
  131142. products
  131143. employing
  131144. intra
  131145. syntheses
  131146. prismanes
  131147. syntheses
  131148. seven
  131149. five-membered
  131150. rings
  131151. allyl
  131152. cation
  131153. syntheses
  131154. natural
  131155. products
  131156. using
  131157. zirconium-promoted
  131158. syntheses
  131159. first
  131160. selenium
  131161. containing
  131162. bicyclic
  131163. lactam
  131164. syntheses
  131165. structures
  131166. properties
  131167. methanofullerenes
  131168. syntheses
  131169. structures
  131170. bonding
  131171. reactivity
  131172. group
  131173. syntheses
  131174. vinyl
  131175. sulfones
  131176. highly
  131177. efficient
  131178. synthesis
  131179. syntheses
  131180. polyfunctional
  131181. organomagnesium
  131182. compounds
  131183. synthesi
  131184. synthesisD
  131185. synthesis
  131186. synthesis
  131187. synthesis
  131188. synthesis
  131189. synthesis
  131190. synthesis
  131191. synthesis
  131192. synthesis
  131193. synthesis
  131194. synthesis
  131195. synthesis
  131196. synthesis
  131197. synthesis
  131198. synthesis
  131199. synthesis
  131200. synthesis
  131201. synthesis
  131202. synthesis
  131203. synthesis
  131204. synthesis
  131205. synthesis
  131206. asymmetric
  131207. diels
  131208. alder
  131209. reactions
  131210. chiral
  131211. synthesis
  131212. asymmetric
  131213. diels-alder
  131214. reactions
  131215. chiral
  131216. synthesis
  131217. biological
  131218. activities
  131219. condensed
  131220. heterocyclo
  131221. synthesis
  131222. biological
  131223. activity
  131224. novel
  131225. synthesis
  131226. biological
  131227. evaluation
  131228. epibatidine
  131229. conge
  131230. synthesis
  131231. biological
  131232. properties
  131233. selected
  131234. nucleoside
  131235. synthesis
  131236. characterization
  131237. coumarin-crown
  131238. ethers
  131239. synthesis
  131240. characterization
  131241. expanded
  131242. thiophene
  131243. synthesis
  131244. characterization
  131245. nine-membered
  131246. cyclic
  131247. enedi
  131248. synthesis
  131249. characterization
  131250. anhydro
  131251. cyclodextri
  131252. synthesis
  131253. characterization
  131254. rhenium
  131255. metallocarboxylate
  131256. synthesis
  131257. chemistry
  131258. silanes
  131259. synthesis
  131260. chemistry
  131261. benzocyclopropenes
  131262. synthesis
  131263. chemistry
  131264. cubanes
  131265. synthesis
  131266. chemistry
  131267. homocubanes
  131268. bishomocubanes
  131269. synthesis
  131270. chemistry
  131271. heteroatom
  131272. systems
  131273. containing
  131274. synthesis
  131275. chemistry
  131276. heteroatom
  131277. systems
  131278. containing
  131279. synthesis
  131280. conformation
  131281. phosphodiester
  131282. synthesis
  131283. conformational
  131284. analysis
  131285. sugars
  131286. synthesis
  131287. diels
  131288. alder
  131289. reactions
  131290. facially
  131291. dissymmetr
  131292. synthesis
  131293. flash
  131294. vacuum
  131295. pyrolysis
  131296. isoxazolo
  131297. pyrim
  131298. synthesis
  131299. hypolipidemic
  131300. activity
  131301. novel
  131302. benzo
  131303. synthesis
  131304. mechanism
  131305. formation
  131306. lactams
  131307. synthesis
  131308. mercury
  131309. trifluoroacetate
  131310. mediated
  131311. cyclizati
  131312. synthesis
  131313. photophysical
  131314. study
  131315. monoaza
  131316. crown
  131317. synthesis
  131318. properties
  131319. trimethylphenylboran
  131320. mesityl
  131321. synthesis
  131322. properties
  131323. alpha-amino
  131324. nitriles
  131325. synthesis
  131326. properties
  131327. double-calix
  131328. arenes
  131329. doubly-cro
  131330. synthesis
  131331. properties
  131332. tetramethyloctadehyd
  131333. synthesis
  131334. prototropic
  131335. tautomerism
  131336. alkyl
  131337. methyl
  131338. synthesis
  131339. reaction
  131340. thioaldehydes
  131341. wittig
  131342. reagents
  131343. synthesis
  131344. reactions
  131345. 2-alkyl-13-cyclopent
  131346. synthesis
  131347. reactions
  131348. trimethylsilyl
  131349. furan
  131350. diels
  131351. synthesis
  131352. reactions
  131353. trifluoromethanesulf
  131354. enecarbama
  131355. synthesis
  131356. reactions
  131357. alkynylamines
  131358. synthesis
  131359. reactions
  131360. alpha-haloalkyl
  131361. isocyanates
  131362. synthesis
  131363. reactions
  131364. alpha-hydroxylamino
  131365. oximes
  131366. synthesis
  131367. reactions
  131368. fluoroalkanesulfonyl
  131369. azides
  131370. synthesis
  131371. reactions
  131372. functionalized
  131373. silyl
  131374. ethers
  131375. synthesis
  131376. reactions
  131377. glutaconaldehyde
  131378. 5-amino-24-p
  131379. synthesis
  131380. reactions
  131381. ketenimines
  131382. synthesis
  131383. reactions
  131384. lithiated
  131385. monocyclic
  131386. azoles
  131387. conta
  131388. synthesis
  131389. reactions
  131390. methylene
  131391. sulfones
  131392. synthesis
  131393. reactions
  131394. monosilylated
  131395. hexatriyne
  131396. synthesis
  131397. reactions
  131398. n-substituted
  131399. pyrimidinones
  131400. synthesis
  131401. reactions
  131402. phosphine-boranes
  131403. synthesis
  131404. reactions
  131405. novel
  131406. tropono
  131407. oxepines
  131408. synthesis
  131409. reactions
  131410. 2-alkyl-13-cyclopent@
  131411. synthesis
  131412. reactions
  131413. optic
  131414. lly-active
  131415. cyanohydrins@
  131416. synthesis
  131417. structures
  131418. functionalized
  131419. cyclopropylsilane@
  131420. synthesis
  131421. substituted
  131422. indoles
  131423. substituted
  131424. triazi@
  131425. synthesis
  131426. substituted
  131427. enoic
  131428. acids
  131429. palladium
  131430. synthesis
  131431. amino
  131432. acids
  131433. addition
  131434. putative
  131435. azido
  131436. synthesis
  131437. aldehydes
  131438. ketones
  131439. carboxylic
  131440. acids
  131441. synthesis
  131442. arylcycloalkanes
  131443. alkenyl
  131444. benzylselenides@
  131445. synthesis
  131446. biologically
  131447. active
  131448. pseudo-oligosacchari@
  131449. synthesis
  131450. castasterone
  131451. formal
  131452. synthesis
  131453. brassinoli@
  131454. synthesis
  131455. cyclohexene
  131456. dicarbaldehydes
  131457. diels
  131458. alder
  131459. synthesis
  131460. enantiomeric
  131461. amino
  131462. ketones
  131463. dipolar
  131464. synthesis
  131465. haloesters
  131466. ketoesters
  131467. homolytic
  131468. addi@
  131469. synthesis
  131470. imidazolinones
  131471. azetidinones
  131472. formazans
  131473. synthesis
  131474. phenylsulfonyl
  131475. protected
  131476. pyrroles
  131477. synthesis
  131478. reactions
  131479. optic
  131480. lly-active
  131481. cyanohydrins
  131482. synthesis
  131483. reactions
  131484. stable
  131485. nitroxyl
  131486. radicals
  131487. synthe
  131488. synthesis
  131489. reactions
  131490. alkynylamines
  131491. synthesis
  131492. reactions
  131493. vinylic
  131494. organoboranes
  131495. synthesis
  131496. reactivity
  131497. substituted
  131498. pyrrolo
  131499. synthesis
  131500. reactivity
  131501. lambda5-phosphazenes
  131502. synthesis
  131503. reactivity
  131504. n-substituted
  131505. aminoamides
  131506. antiar
  131507. synthesis
  131508. reactivity
  131509. oxazolopiperidines
  131510. oxazolopi
  131511. synthesis
  131512. reactivity
  131513. thiochroman
  131514. diones
  131515. synthesis
  131516. reactivity
  131517. sugars
  131518. branches
  131519. synthesis
  131520. reactivity
  131521. first
  131522. crown
  131523. ether
  131524. enediy
  131525. synthesis
  131526. properties
  131527. alkenyl
  131528. carbanions
  131529. stabiliz
  131530. synthesis
  131531. spectroscopic
  131532. properties
  131533. phthalocyanine
  131534. synthesis
  131535. structure
  131536. soluble
  131537. organosamarium
  131538. synthesis
  131539. structure
  131540. first
  131541. titanium
  131542. amino
  131543. synthesis
  131544. structures
  131545. functionalized
  131546. cyclopropylsilane
  131547. synthesis
  131548. synthetic
  131549. applications
  131550. donor
  131551. substituted
  131552. synthesis
  131553. synthetic
  131554. applications
  131555. 1-donor
  131556. substituted
  131557. synthesis
  131558. synthetic
  131559. applications
  131560. 1-metallo-1-seleno-c
  131561. synthesis
  131562. synthetic
  131563. potential
  131564. acylsilanes
  131565. synthesis
  131566. synthetic
  131567. utility
  131568. halolactones
  131569. synthesis
  131570. therapeutic
  131571. potential
  131572. hydroxamic
  131573. based
  131574. synthesis
  131575. acids
  131576. synthesis
  131577. utilisation
  131578. compounds
  131579. chiral
  131580. nitrogen
  131581. synthesis
  131582. utilization
  131583. compounds
  131584. chiral
  131585. silicon
  131586. synthesis
  131587. structure
  131588. zirconocene
  131589. complex
  131590. synthesis
  131591. indispensable
  131592. study
  131593. chemical
  131594. synthesis
  131595. conformations
  131596. x-ray
  131597. structure
  131598. analysis
  131599. synthesis
  131600. electronic
  131601. structure
  131602. reactivity
  131603. metallacycl
  131604. synthesis
  131605. alkylimidazoles
  131606. synthesis
  131607. silyl
  131608. indolene
  131609. anionic
  131610. silyl
  131611. group
  131612. synthesis
  131613. substituted
  131614. indoles
  131615. substituted
  131616. triazi
  131617. synthesis
  131618. dicarbonyl
  131619. compounds
  131620. cyclopentenones
  131621. synthesis
  131622. diketones
  131623. review
  131624. synthesis
  131625. 14-dicarbonyl
  131626. compounds
  131627. cyclopentenones
  131628. synthesis
  131629. 14-dihydropyridines
  131630. cyclocondensation
  131631. reacti
  131632. synthesis
  131633. methano
  131634. annulenopyridines
  131635. tandem
  131636. synthesis
  131637. 16-didehydro
  131638. annulene
  131639. observation
  131640. synthesis
  131641. fluoro-substituted
  131642. nucleosides
  131643. direct
  131644. synthesis
  131645. tributylstannyl
  131646. alkenes
  131647. tributylstan
  131648. synthesis
  131649. 2-pyrazolines
  131650. 35-pyrazolidinedione
  131651. synthesis
  131652. 2.2.3
  131653. cyclazines
  131654. 2.2.3
  131655. cyclazines
  131656. their
  131657. synthesis
  131658. pyrazolo
  131659. pyridin
  131660. cyclization
  131661. synthesis
  131662. alkynylpyridazines
  131663. trifluoromethanesul
  131664. synthesis
  131665. alkylamino
  131666. acetophenones
  131667. benzyne
  131668. synthesis
  131669. dihydroisoquinolines
  131670. ethyl
  131671. synthesis
  131672. substituted
  131673. enoic
  131674. acids
  131675. palladium
  131676. synthesis
  131677. 3-pyridylpropenoic
  131678. esters
  131679. couplin
  131680. synthesis
  131681. disubstituted
  131682. pyrroles
  131683. bearing
  131684. substituents
  131685. synthesis
  131686. benzotriazepines
  131687. aryltetrazoles
  131688. synthesis
  131689. hydroxy
  131690. alkoxyquinolinequino
  131691. using
  131692. synthesis
  131693. disubstituted
  131694. dihydro
  131695. furanones
  131696. contain
  131697. synthesis
  131698. membered
  131699. phosphorus
  131700. heterocycles
  131701. synthesis
  131702. 7-membered
  131703. phosphorus
  131704. heterocycles
  131705. synthesis
  131706. substituted
  131707. guanines
  131708. synthesis
  131709. 9-substituted
  131710. guanines
  131711. synthesis
  131712. membered
  131713. intramolecular
  131714. synthesis
  131715. tetrasubstituted
  131716. lactones
  131717. ketone
  131718. synthesis
  131719. dialkoxy
  131720. imines
  131721. acetals
  131722. synthesis
  131723. alkinylenamines
  131724. trimethylsilanolate
  131725. induce
  131726. synthesis
  131727. amidoketones
  131728. application
  131729. multi
  131730. synthesis
  131731. amino
  131732. acids
  131733. addition
  131734. putative
  131735. azido
  131736. synthesis
  131737. azido
  131738. aldehydes
  131739. stereoselective
  131740. formal
  131741. access
  131742. synthesis
  131743. epoxyesters
  131744. homolytically
  131745. induced
  131746. decomp
  131747. synthesis
  131748. benzylamidine
  131749. derived
  131750. mannose
  131751. potent
  131752. synthesis
  131753. taxinine
  131754. intermediate
  131755. using
  131756. synthesis
  131757. cancer
  131758. growth-inhibiting
  131759. diterpene
  131760. spatol
  131761. synthesis
  131762. dynamycin
  131763. analogue
  131764. bergman-type
  131765. synthesis
  131766. intermediate
  131767. preparation
  131768. didehy
  131769. synthesis
  131770. stable
  131771. tributylstannyl
  131772. butadiene
  131773. precurs
  131774. synthesis
  131775. trimethylsilylalleno
  131776. synthesis
  131777. a-amido
  131778. ketones
  131779. application
  131780. multi
  131781. synthesis
  131782. model
  131783. system
  131784. taxol
  131785. allylation
  131786. synthesis
  131787. acetals
  131788. alkenes
  131789. hydroformylatio
  131790. synthesis
  131791. halides
  131792. anhydrides
  131793. related
  131794. compounds
  131795. synthesis
  131796. alcohols
  131797. ethers
  131798. synthesis
  131799. aldehydes
  131800. ketones
  131801. carboxylic
  131802. acids
  131803. synthesis
  131804. alkaloidal
  131805. compounds
  131806. using
  131807. electrochemical
  131808. synthesis
  131809. alkyl
  131810. substituted
  131811. pyridines
  131812. synthesis
  131813. alkynes
  131814. ethers
  131815. synthesis
  131816. allenes
  131817. palladium
  131818. catalyzed
  131819. cross
  131820. coupling
  131821. synthesis
  131822. alpha
  131823. omega
  131824. alkanediols
  131825. review
  131826. synthesis
  131827. alpha
  131828. omega-alkanediols
  131829. review
  131830. synthesis
  131831. alpha-amino
  131832. aldehydes
  131833. alpha-amino
  131834. ketones
  131835. synthesis
  131836. amides
  131837. related
  131838. compounds
  131839. synthesis
  131840. amines
  131841. ammonium
  131842. salts
  131843. synthesis
  131844. amines
  131845. intermolecular
  131846. schmidt
  131847. reaction
  131848. synthesis
  131849. elicitor-active
  131850. analogue
  131851. one-pot
  131852. synthesis
  131853. angular
  131854. benzodipyrazoles
  131855. related
  131856. systems
  131857. synthesis
  131858. anthracyclinones
  131859. electrophilic
  131860. nucleophi
  131861. synthesis
  131862. antibiotic
  131863. hygromycin-a
  131864. derivatives
  131865. synthesis
  131866. aromatic
  131867. heterocycles
  131868. palladium-catalyzed
  131869. synthesis
  131870. arylcycloalkanes
  131871. alkenyl
  131872. benzylselenides
  131873. synthesis
  131874. aza-crown
  131875. ethers
  131876. synthesis
  131877. azaphenalenes
  131878. synthesis
  131879. alkylserine
  131880. carboxyanhydrides
  131881. through
  131882. synthesis
  131883. hydroxy
  131884. trimethylsilyl
  131885. butyrolactone
  131886. synthesis
  131887. hydroxy
  131888. nitriles
  131889. indium
  131890. induced
  131891. coupling
  131892. synthesis
  131893. lactams
  131894. condensation
  131895. enolates
  131896. synthesis
  131897. trimethylsilyl
  131898. unsaturated
  131899. ketones
  131900. synthesis
  131901. b-lactam
  131902. derivatives
  131903. cycloaddition
  131904. synthesis
  131905. benzo
  131906. naphthyridines
  131907. palladium
  131908. catalyze
  131909. synthesis
  131910. benzoquinones
  131911. oxidation
  131912. synthesis
  131913. benzoquinones
  131914. oxidation
  131915. james
  131916. cason
  131917. organic
  131918. synthesis
  131919. beta-lactams
  131920. unsaturated
  131921. sugars
  131922. isocya
  131923. synthesis
  131924. beta-oxygenated
  131925. gamma-amino
  131926. acids
  131927. gamma-oxy
  131928. synthesis
  131929. bioactive
  131930. sialosides
  131931. synthesis
  131932. biologically
  131933. active
  131934. compounds
  131935. composed
  131936. carba
  131937. synthesis
  131938. biologically
  131939. active
  131940. pseudo-oligosacchari
  131941. synthesis
  131942. biologically
  131943. active
  131944. sialo-compounds
  131945. synthesis
  131946. bridgehead
  131947. enones
  131948. synthesis
  131949. glycosides
  131950. synthesis
  131951. c-aryl
  131952. glycosides
  131953. synthesis
  131954. carbazole
  131955. alkaloids
  131956. synthesis
  131957. carbo
  131958. heterocyclic
  131959. compounds
  131960. radical
  131961. synthesis
  131962. carbocyclic
  131963. nucleosides
  131964. synthesis
  131965. carbocyclic
  131966. spiro
  131967. compounds
  131968. rearrangement
  131969. synthesis
  131970. carbocyclic
  131971. systems
  131972. radical
  131973. induced
  131974. epoxide
  131975. synthesis
  131976. carboxylic
  131977. acids
  131978. esters
  131979. carbonylation
  131980. synthesis
  131981. carboxylic
  131982. acids
  131983. esters
  131984. their
  131985. derivatives
  131986. synthesis
  131987. carboxylic
  131988. carbonic
  131989. ortho
  131990. esters
  131991. synthesis
  131992. carcinogenic
  131993. acridines
  131994. synthesis
  131995. carcinogenic
  131996. acridines
  131997. review
  131998. synthesis
  131999. carcinogenic
  132000. oxygenated
  132001. derivatives
  132002. synthesis
  132003. carpyrinic
  132004. related
  132005. pyridines
  132006. synthesis
  132007. castasterone
  132008. formal
  132009. synthesis
  132010. brassinoli
  132011. synthesis
  132012. cembranoid
  132013. natural
  132014. products
  132015. intramolecular
  132016. synthesis
  132017. chiral
  132018. bioactive
  132019. fluoroorganic
  132020. compounds
  132021. synthesis
  132022. chiral
  132023. carbocyclic
  132024. nucleosides
  132025. synthesis
  132026. chiral
  132027. d-unsaturated
  132028. amino
  132029. acids
  132030. asymmetri
  132031. synthesis
  132032. chiral
  132033. lactams
  132034. templates
  132035. enzyme
  132036. inhibito
  132037. synthesis
  132038. compounds
  132039. containing
  132040. adjacent
  132041. labels
  132042. synthesis
  132043. condensed
  132044. 124-triazol
  132045. heter
  132046. cycles
  132047. synthesis
  132048. condensed
  132049. heteroaromatic
  132050. compounds
  132051. using
  132052. pallad
  132053. synthesis
  132054. condensed
  132055. thiazolo
  132056. yrimidine
  132057. systems
  132058. synthesis
  132059. conformationally
  132060. restricted
  132061. amino
  132062. acids
  132063. synthesis
  132064. coumarins
  132065. 3:4-fused
  132066. systems
  132067. their
  132068. synthesis
  132069. related
  132070. zirconocene
  132071. synthesis
  132072. cularine
  132073. sarcocapnine
  132074. enium
  132075. synthesis
  132076. curacin
  132077. powerful
  132078. antimitotic
  132079. cyano
  132080. synthesis
  132081. cyclohexene
  132082. dicarbaldehydes
  132083. diels
  132084. alder
  132085. synthesis
  132086. cyclopenta
  132087. indoles
  132088. formal
  132089. addition
  132090. synthesis
  132091. cyclopentylamines
  132092. using
  132093. zirconium
  132094. chemistry
  132095. synthesis
  132096. cyclopropane
  132097. amino
  132098. acids
  132099. their
  132100. incorporatio
  132101. synthesis
  132102. cyclopropyl
  132103. ethers
  132104. cyclopropanols
  132105. carben
  132106. synthesis
  132107. cyclopropylcarbinyl
  132108. compounds
  132109. synthesis
  132110. oxazolines
  132111. oxazines
  132112. using
  132113. potas
  132114. synthesis
  132115. deoxy
  132116. xylolactone
  132117. glycerol
  132118. derivatives
  132119. synthesis
  132120. polyphosphane
  132121. phosphene
  132122. transiti
  132123. synthesis
  132124. diallylamines
  132125. triallylamines
  132126. acetoxy
  132127. synthesis
  132128. dicarboxylic
  132129. acids
  132130. transition-metal
  132131. alyze
  132132. synthesis
  132133. dihydropyranones
  132134. their
  132135. application
  132136. synthesis
  132137. diquinane
  132138. triquinane
  132139. sesquiterpenes
  132140. diterpe
  132141. synthesis
  132142. interactive
  132143. pyrrolo
  132144. benzodiazepines
  132145. synthesis
  132146. dna-interactive
  132147. pyrrolo
  132148. benzodiazepines
  132149. synthesis
  132150. enantiomeric
  132151. amino
  132152. ketones
  132153. dipolar
  132154. synthesis
  132155. enantiomerically
  132156. substituted
  132157. synthesis
  132158. enantiomerically
  132159. anti-aldols
  132160. highly
  132161. synthesis
  132162. enantiomerically
  132163. difluorocyclohexane
  132164. synthesis
  132165. enantiomerically
  132166. secondary
  132167. amma-halo
  132168. allyl
  132169. synthesis
  132170. enantiopure
  132171. malonylvinyl
  132172. sulfoxides
  132173. addit
  132174. synthesis
  132175. enediynes
  132176. diels
  132177. alder
  132178. addition
  132179. synthesis
  132180. esters
  132181. activated
  132182. esters
  132183. lactones
  132184. synthesis
  132185. exo-enynes
  132186. ruthenium-catalyzed
  132187. cross
  132188. couplin
  132189. synthesis
  132190. five-membered
  132191. aromatic
  132192. heterocycles
  132193. synthesis
  132194. five-membered
  132195. rings
  132196. heteroatom
  132197. synthesis
  132198. five-membered
  132199. rings
  132200. heteroatom
  132201. synthesis
  132202. fredericamycin
  132203. synthesis
  132204. functionalised
  132205. vinyl
  132206. triflates
  132207. terminal
  132208. synthesis
  132209. functionalized
  132210. hydroazulenes
  132211. approach
  132212. ynthesis
  132213. fused
  132214. heterocycles
  132215. synthesis
  132216. haloesters
  132217. ketoesters
  132218. homolytic
  132219. synthesis
  132220. glycol
  132221. synthesis
  132222. glycosides
  132223. synthesis
  132224. glycosyl
  132225. phosphonates
  132226. related
  132227. compounds
  132228. synthesis
  132229. halides
  132230. synthesis
  132231. helically
  132232. chiral
  132233. molecules
  132234. stereoselective
  132235. rocycles
  132236. aza-wittig
  132237. reaction
  132238. synthesis
  132239. heterocycles
  132240. aminoamide
  132241. oximes
  132242. synthesis
  132243. heterocycles
  132244. azadienes
  132245. synthesis
  132246. heterocycles
  132247. ketene
  132248. dithioacetals
  132249. synthesis
  132250. heterocycles
  132251. using
  132252. aminoacetals
  132253. synthesis
  132254. heterocycles
  132255. using
  132256. thioamide
  132257. groups
  132258. synthesis
  132259. heterocyclic
  132260. compounds
  132261. involving
  132262. aromatic
  132263. lithi
  132264. synthesis
  132265. highly
  132266. functionalized
  132267. 7-azabicyclo
  132268. 2.2.1
  132269. heptad
  132270. synthesis
  132271. homochiral
  132272. amino
  132273. alcohols
  132274. aziridines
  132275. synthesis
  132276. homopeptides
  132277. amino
  132278. acids
  132279. synthesis
  132280. homopeptides
  132281. amino
  132282. acids
  132283. other
  132284. compoun
  132285. synthesis
  132286. homopropargyl
  132287. cycloalkanols
  132288. palladium
  132289. cataly
  132290. synthesis
  132291. imidazolinones
  132292. azetidinones
  132293. formazans
  132294. synthesis
  132295. iminium
  132296. salts
  132297. orthoesters
  132298. related
  132299. compounds
  132300. synthesis
  132301. indenones
  132302. palladium
  132303. catalyzed
  132304. annulation
  132305. synthesis
  132306. insect
  132307. pheromones
  132308. synthesis
  132309. inversely-fused
  132310. bicyclic
  132311. b-lactams
  132312. synthesis
  132313. jatrophone
  132314. synthesis
  132315. lactones
  132316. lactams
  132317. updates
  132318. chemistry
  132319. synthesis
  132320. laurencin
  132321. synthesis
  132322. leukotrienes
  132323. lipoxygenase
  132324. products
  132325. synthesis
  132326. lycorines
  132327. intramolecular
  132328. aryne
  132329. cycloaddition
  132330. synthesis
  132331. macrocyclic
  132332. compounds
  132333. enlargement
  132334. synthesis
  132335. macrocyclic
  132336. trichothecene
  132337. mycotoxins
  132338. synthesis
  132339. macrolides
  132340. synthesis
  132341. materials
  132342. molecular
  132343. electronic
  132344. applications
  132345. synthesis
  132346. medio-and
  132347. macrocyclic
  132348. compounds
  132349. dilutio
  132350. synthesis
  132351. medium
  132352. large
  132353. rings
  132354. synthesis
  132355. bridge
  132356. synthesis
  132357. medium
  132358. cycloalkynes
  132359. synthesis
  132360. phenylsulfonyl
  132361. protected
  132362. pyrroles
  132363. synthesis
  132364. phenylsulfonyl
  132365. protected
  132366. pyrroles
  132367. synthesis
  132368. naphthoquinone
  132369. nucleus
  132370. awamycin
  132371. synthesis
  132372. naphthyridinomycin
  132373. synthesis
  132374. natural
  132375. products
  132376. isoxazoles
  132377. synthesis
  132378. substituted
  132379. furyl
  132380. pyrans
  132381. synthesis
  132382. spiropyrrolidines
  132383. michael
  132384. addition
  132385. synthesis
  132386. taxoids
  132387. synthesis
  132388. torands
  132389. torands
  132390. synthesis
  132391. nitro-derivatives
  132392. triazoles
  132393. synthesis
  132394. nitrogen
  132395. containing
  132396. heterocycles
  132397. imino
  132398. synthesis
  132399. nitrogen
  132400. heterocycles
  132401. using
  132402. tandem
  132403. radical
  132404. synthesis
  132405. nitroso
  132406. nitro
  132407. related
  132408. compounds
  132409. synthesis
  132410. non-natural
  132411. products
  132412. challenge
  132413. reward
  132414. synthesis
  132415. nonaromatic
  132416. heterocyclic
  132417. compounds
  132418. through
  132419. synthesis
  132420. novel
  132421. diaryltetrahydro
  132422. oxazine
  132423. thion
  132424. synthesis
  132425. novel
  132426. benzenoid
  132427. molecules
  132428. valent
  132429. titaniu
  132430. synthesis
  132431. novel
  132432. benzenoid
  132433. molecules
  132434. valent-titaniu
  132435. synthesis
  132436. novel
  132437. oligosaccharides
  132438. synthesis
  132439. novel
  132440. taxoids
  132441. synthesis
  132442. nucleosides
  132443. containing
  132444. condensed
  132445. pyrimidine
  132446. synthesis
  132447. nucleosides
  132448. derived
  132449. other
  132450. heterocyclic
  132451. synthesis
  132452. nuphar
  132453. piperidine
  132454. alkaloids
  132455. anhydronupharamine
  132456. synthesis
  132457. oligonucleotide
  132458. analogs
  132459. modified
  132460. backbones
  132461. synthesis
  132462. oligosaccharides
  132463. 2-amino-2-deoxy
  132464. sugars
  132465. synthesis
  132466. oligosaccharides
  132467. related
  132468. bacterial
  132469. o-antigen
  132470. synthesis
  132471. oligosaccharides
  132472. related
  132473. plant
  132474. vertebrate
  132475. synthesis
  132476. optical
  132477. active
  132478. pheromones
  132479. synthesis
  132480. optically
  132481. active
  132482. isopropylidene
  132483. trimethy
  132484. synthesis
  132485. optically
  132486. active
  132487. alpha-amino
  132488. acids
  132489. synthesis
  132490. optically
  132491. active
  132492. calanolides
  132493. synthesis
  132494. optically
  132495. active
  132496. carotenoids
  132497. review
  132498. synthesis
  132499. optically
  132500. active
  132501. compounds
  132502. large
  132503. scale
  132504. perspe
  132505. synthesis
  132506. optically
  132507. active
  132508. muscone
  132509. synthesis
  132510. optically
  132511. active
  132512. pheromones
  132513. synthesis
  132514. novel
  132515. oligosaccharides@
  132516. synthesis
  132517. optically
  132518. active
  132519. tetracyclic
  132520. quassinoid
  132521. skeleto@
  132522. synthesis
  132523. perfluoro-oxa-alkyla
  132524. compounds
  132525. synthesis
  132526. poylcyclic
  132527. cyclobutane
  132528. derivatives
  132529. tandem
  132530. synthesis
  132531. quassinoids
  132532. review@
  132533. synthesis
  132534. substituted
  132535. pyridines
  132536. thieno
  132537. synthesis
  132538. taxol
  132539. baccatin
  132540. oxazoline
  132541. interme@
  132542. synthesis
  132543. indole
  132544. alkaloid
  132545. alpha-cyclopiazonic
  132546. synthesis
  132547. unsymmetrical
  132548. biaryls
  132549. kinetic
  132550. higher
  132551. order
  132552. synthesis
  132553. structure
  132554. reactivity
  132555. cyclopenta
  132556. annulated
  132557. synthetic
  132558. synthetic
  132559. applications
  132560. enantioselective
  132561. organotransition-@
  132562. synthetic
  132563. approaches
  132564. ellipticines
  132565. other
  132566. derivatives
  132567. synthetic
  132568. chemistry
  132569. stable
  132570. nitroxides@
  132571. synthetic
  132572. organoindium
  132573. chemistry
  132574. makes
  132575. indium
  132576. appeal@
  132577. synthetic
  132578. routes
  132579. 25-disubstituted
  132580. tetrahydrofurans@
  132581. synthesis
  132582. optically
  132583. active
  132584. tetracyclic
  132585. quassinoid
  132586. skeleto
  132587. synthesis
  132588. optically
  132589. gosisin
  132590. total
  132591. synthesis
  132592. synthesis
  132593. organophospho
  132594. compounds
  132595. coordination
  132596. synthesis
  132597. oxabicyclo
  132598. undecenone
  132599. derivatives
  132600. synthesis
  132601. oxygen-containing
  132602. heterocycles
  132603. using
  132604. palladium
  132605. synthesis
  132606. peptides
  132607. containing
  132608. a-dialkyl
  132609. aminoacids
  132610. synthesis
  132611. peptides
  132612. mixed
  132613. anhydrides
  132614. synthesis
  132615. peptidyl
  132616. ruthenium
  132617. p-arene
  132618. complexes
  132619. applicatio
  132620. synthesis
  132621. peri-annelated
  132622. heterocyclic
  132623. systems
  132624. synthesis
  132625. phenanthrenes
  132626. synthesis
  132627. phorbol
  132628. ester
  132629. pyrylinn
  132630. alkene
  132631. cycloadd
  132632. synthesis
  132633. phosphonium
  132634. ylides
  132635. synthesis
  132636. phosphorus-containin
  132637. macrocycles
  132638. cryptands
  132639. synthesis
  132640. podophyllotoxin
  132641. related
  132642. compounds
  132643. synthesis
  132644. polycyclics
  132645. aryne
  132646. arylation
  132647. reactions
  132648. synthesis
  132649. polyenes
  132650. phosphonium
  132651. ylides
  132652. synthesis
  132653. polypeptides
  132654. synthesis
  132655. poylcyclic
  132656. cyclobutane
  132657. derivatives
  132658. tandem
  132659. synthesis
  132660. primary
  132661. allylic
  132662. amines
  132663. synthesis
  132664. primory
  132665. allylic
  132666. amines
  132667. synthesis
  132668. proaporphine
  132669. alkaloids
  132670. synthesis
  132671. prostaglandins
  132672. synthesis
  132673. prostaglandins
  132674. conjugate
  132675. addition
  132676. alkyla
  132677. synthesis
  132678. protected
  132679. oxopipecolic
  132680. oxolysine
  132681. synthesis
  132682. pseudohalides
  132683. nitriles
  132684. related
  132685. compounds
  132686. synthesis
  132687. pyran
  132688. pyrazoles
  132689. synthesis
  132690. pyranotropanes
  132691. enantioselective
  132692. deprotonati
  132693. synthesis
  132694. pyridoacridines
  132695. synthesis
  132696. pyrimidine
  132697. derivatives
  132698. their
  132699. related
  132700. compou
  132701. synthesis
  132702. pyrimidine
  132703. nucleosides
  132704. synthesis
  132705. pyrroles
  132706. aliphatic
  132707. compounds
  132708. synthesis
  132709. pyrrolidine
  132710. piperidine
  132711. palladium
  132712. cataly
  132713. synthesis
  132714. pyrrolidines
  132715. piperidines
  132716. palladium
  132717. synthesis
  132718. pyrrolidinones
  132719. radical
  132720. cyclisations
  132721. synthesis
  132722. pyrrolizidine
  132723. oximes
  132724. novel
  132725. alkaloid
  132726. synthesis
  132727. quassinoids
  132728. review
  132729. synthesis
  132730. 78-epoxy-4-basmen-6
  132731. transannular
  132732. cycli
  132733. synthesis
  132734. rac-78-epoxy-4-basme
  132735. transannular
  132736. cyclizat
  132737. synthesis
  132738. rac-78-epoxy-4-basme
  132739. transannular
  132740. strategy
  132741. synthesis
  132742. racemic
  132743. epibatidine
  132744. natural
  132745. product
  132746. synthesis
  132747. radiolabeled
  132748. compounds
  132749. organometallic
  132750. inter
  132751. synthesis
  132752. regiospecifically
  132753. substituted
  132754. pyrimidyl
  132755. derivat
  132756. synthesis
  132757. rearranged
  132758. taxane
  132759. analogs
  132760. synthesis
  132761. saframycins
  132762. efficient
  132763. synthesis
  132764. synthesis
  132765. selenium
  132766. tellurium
  132767. ylides
  132768. carbanions
  132769. synthesis
  132770. seven-membered
  132771. heterocycles
  132772. pericyclic
  132773. synthesis
  132774. several
  132775. substituted
  132776. amino
  132777. pyridones
  132778. synthesis
  132779. sialic
  132780. analogs
  132781. their
  132782. behavior
  132783. towards
  132784. synthesis
  132785. six-membered
  132786. rings
  132787. synthesis
  132788. small
  132789. large
  132790. rings
  132791. synthesis
  132792. small
  132793. cyclophanes
  132794. synthesis
  132795. substituted
  132796. pyridines
  132797. thieno
  132798. synthesis
  132799. substituted
  132800. pyridines
  132801. thieno
  132802. synthesis
  132803. bridgehead
  132804. bridgehead
  132805. disubstituted
  132806. bicycl
  132807. synthesis
  132808. carbocyclic
  132809. nucleoside
  132810. analogues
  132811. based
  132812. synthesis
  132813. uridine
  132814. derivatives
  132815. formation
  132816. synthesis
  132817. spirodecane
  132818. system
  132819. through
  132820. allylsilane
  132821. synthesis
  132822. spirone
  132823. piperidine-4
  132824. c'n-hetero
  132825. carbo
  132826. cycles
  132827. synthesis
  132828. stereodefined
  132829. enynes
  132830. nickel
  132831. catalyzed
  132832. synthesis
  132833. stilbenes
  132834. synthesis
  132835. strychnine
  132836. wieland-gumlich
  132837. aldehyde
  132838. synthesis
  132839. substituted
  132840. cyclooctanols
  132841. samarium
  132842. synthesis
  132843. substituted
  132844. dioxabicyclo
  132845. alkanes
  132846. through
  132847. synthesis
  132848. substituted
  132849. ferrocenes
  132850. other
  132851. cyclopentadien
  132852. synthesis
  132853. sulfides
  132854. sulfoxides
  132855. sulfones
  132856. synthesis
  132857. sulfoxides
  132858. oxidation
  132859. thioesters
  132860. synthesis
  132861. sulfoxides
  132862. oxidation
  132863. thioethers
  132864. synthesis
  132865. homopropargylic
  132866. allenic
  132867. alcoho
  132868. synthesis
  132869. taxol
  132870. baccatin
  132871. oxazoline
  132872. interme
  132873. synthesis
  132874. amaryllidaceae
  132875. alkaloids
  132876. synthesis
  132877. anthraquinone
  132878. dynemicin
  132879. diels
  132880. synthesis
  132881. bicycl
  132882. 5.3.1
  132883. undecane
  132884. moiety
  132885. system
  132886. synthesis
  132887. bicyclic
  132888. zaragozic
  132889. acids
  132890. squale
  132891. 25-furanocyclic
  132892. system
  132893. synthesis
  132894. taxol
  132895. derivatives
  132896. control
  132897. atropisomerism
  132898. synthesis
  132899. tetracyclic
  132900. mitomycin
  132901. skeleton
  132902. dialky
  132903. synthesis
  132904. tricyclo
  132905. 6.2.1.038
  132906. undecan
  132907. skeleton
  132908. synthesis
  132909. therapeutically
  132910. useful
  132911. prostaglandin
  132912. prosta
  132913. synthesis
  132914. thieno
  132915. naphthyridine
  132916. cyanoprop
  132917. synthesis
  132918. substituted
  132919. seleno
  132920. substituted
  132921. methano
  132922. synthesis
  132923. thioamides
  132924. thiolactams
  132925. synthesis
  132926. thioesters
  132927. thiolactones
  132928. synthesis
  132929. trifluorolactic
  132930. epoxy
  132931. trifluor
  132932. synthesis
  132933. tylonolide
  132934. aglycone
  132935. tylosin
  132936. synthesis
  132937. unsymmetrical
  132938. biaryls
  132939. kinetic
  132940. higher
  132941. order
  132942. synthesis
  132943. unsymmetrically
  132944. substituted
  132945. triazoles
  132946. synthesis
  132947. vicinally-substitute
  132948. nitropyridine
  132949. derivatives
  132950. synthesis
  132951. vinca
  132952. alkaloids
  132953. related
  132954. compounds
  132955. synthe
  132956. synthesis
  132957. vinyl
  132958. triflates
  132959. synthesis
  132960. vinylcyclopropanes
  132961. epoxides
  132962. synthesis
  132963. zaragozic
  132964. squalestatin
  132965. synthesis
  132966. reactions
  132967. properties
  132968. oxygen-nitrogen-oxyg
  132969. synthesis
  132970. reactions
  132971. structure
  132972. 1246-thiatriazines
  132973. synthesis
  132974. routes
  132975. metal-alkylidene
  132976. complexes
  132977. synthesis
  132978. stability
  132979. antimicrobial
  132980. activity
  132981. obafluorin
  132982. synthesis
  132983. stereochemistry
  132984. stability
  132985. optically
  132986. active
  132987. synthesis
  132988. structure
  132989. mechanism
  132990. immunophilin
  132991. research
  132992. synthesis
  132993. structure
  132994. reactivity
  132995. rhenium
  132996. vinylalk
  132997. synthesis
  132998. structure
  132999. reactivity
  133000. alpha
  133001. trihalomethyl
  133002. synthesis
  133003. structure
  133004. reactivity
  133005. binuclear
  133006. rhodium
  133007. synthesis
  133008. structure
  133009. reactivity
  133010. cyclopenta
  133011. annulated
  133012. synthesis
  133013. structure
  133014. reactivity
  133015. sulfur-rich
  133016. cyclopenta
  133017. synthesis
  133018. structure
  133019. spectroscopy
  133020. metal-metal
  133021. dimers
  133022. synthesis
  133023. stuttgart
  133024. oxidation
  133025. alcohols
  133026. activat
  133027. synthesis
  133028. stuttgart
  133029. aspects
  133030. stereosclective
  133031. synthesis
  133032. using
  133033. alkyne-derived
  133034. alkenyl
  133035. alkynylaluminium
  133036. synthesis
  133037. oxyphosphoranes
  133038. synthesis
  133039. vinyl
  133040. sulfones
  133041. amelioration
  133042. leaving
  133043. synthesis
  133044. radicals
  133045. formation
  133046. organotin
  133047. synthesis-new
  133048. synthesised
  133049. synthesisof
  133050. synthesized
  133051. synthesizes
  133052. synthesizing
  133053. synthests
  133054. synthet
  133055. synthet
  133056. approaches
  133057. toward
  133058. molecular
  133059. polymeric
  133060. carbon
  133061. syntheticJ
  133062. synthetic
  133063. synthetic
  133064. synthetic
  133065. synthetic
  133066. synthetic
  133067. plications
  133068. organotransition-met
  133069. redox
  133070. reactio
  133071. synthetic
  133072. kinetic
  133073. studies
  133074. substituent
  133075. effects
  133076. synthetic
  133077. anthracyclines
  133078. anthraquinones
  133079. synthetic
  133080. anthracyclines
  133081. anthraquinones
  133082. invited
  133083. review
  133084. synthetic
  133085. application
  133086. pummerer
  133087. reaction
  133088. synthetic
  133089. applications
  133090. involvi
  133091. halogenated
  133092. ketenes
  133093. synthetic
  133094. applications
  133095. dithian
  133096. indoles
  133097. synthetic
  133098. applications
  133099. chlorotrimethylsilan
  133100. synthetic
  133101. applications
  133102. chromium
  133103. tricarbonyl
  133104. stabilized
  133105. synthetic
  133106. applications
  133107. cyanotrimethylsilane
  133108. iodotrimethyl
  133109. synthetic
  133110. applications
  133111. dealkoxycarbonylatio
  133112. malonate
  133113. synthetic
  133114. applications
  133115. diaryl
  133116. ether
  133117. photochemistry
  133118. synthetic
  133119. applications
  133120. diaryl
  133121. ether
  133122. photochemistry
  133123. synthetic
  133124. applications
  133125. dipolar
  133126. cycloaddition
  133127. reactions
  133128. synthetic
  133129. applications
  133130. enantioselective
  133131. organotransition-
  133132. synthetic
  133133. applications
  133134. homolytic
  133135. addition
  133136. telomerisat
  133137. synthetic
  133138. applications
  133139. imidotitanium-alkyne
  133140. cycloaddi
  133141. synthetic
  133142. applications
  133143. intramolecular
  133144. enone
  133145. olefin
  133146. photoc
  133147. synthetic
  133148. applications
  133149. intramolecular
  133150. enone-olefin
  133151. photoc
  133152. synthetic
  133153. applications
  133154. isoxazoles
  133155. synthetic
  133156. applications
  133157. mercury
  133158. photosensitization
  133159. synthetic
  133160. applications
  133161. metalated
  133162. phosphonium
  133163. ylides
  133164. synthetic
  133165. applications
  133166. organoantimony
  133167. compounds
  133168. synthetic
  133169. applications
  133170. organotellurium
  133171. chemistry
  133172. synthetic
  133173. applications
  133174. tellurium
  133175. reagents
  133176. synthetic
  133177. applications
  133178. palladium-cat
  133179. lysed
  133180. oxidation
  133181. synthetic
  133182. applications
  133183. retro-ene
  133184. reaction
  133185. synthetic
  133186. approach
  133187. cuparane
  133188. herbertane
  133189. sesquiterpenoi
  133190. synthetic
  133191. approaches
  133192. biologically
  133193. active
  133194. peptides
  133195. synthetic
  133196. approaches
  133197. butenolides
  133198. synthetic
  133199. approaches
  133200. ellipticines
  133201. other
  133202. derivatives
  133203. synthetic
  133204. approaches
  133205. heteropolynuclear
  133206. pentahalop
  133207. synthetic
  133208. approaches
  133209. stereoisomers
  133210. analogs
  133211. castano
  133212. synthetic
  133213. approaches
  133214. stereoisomers
  133215. analogues
  133216. casta
  133217. synthetic
  133218. approaches
  133219. elliptic
  133220. alkaloids
  133221. metala
  133222. synthetic
  133223. approaches
  133224. vitamin
  133225. synthetic
  133226. approaches
  133227. toward
  133228. antitumor
  133229. quassinoids
  133230. synthetic
  133231. aspects
  133232. applications
  133233. asymmetric
  133234. epoxidation
  133235. synthetic
  133236. aspects
  133237. cycloadditions
  133238. synthetic
  133239. aspects
  133240. aminodeoxy
  133241. sugars
  133242. antibio
  133243. synthetic
  133244. aspects
  133245. diels
  133246. alder
  133247. cycloadditions
  133248. heterod
  133249. synthetic
  133250. aspects
  133251. diels-alder
  133252. ycloadditions
  133253. heterodi
  133254. synthetic
  133255. aspects
  133256. electron-transfer
  133257. chemistry
  133258. synthetic
  133259. aspects
  133260. chemistry
  133261. unsaturated
  133262. amines
  133263. synthetic
  133264. aspects
  133265. fluorination
  133266. organic
  133267. compounds
  133268. synthetic
  133269. aspects
  133270. oxadi
  133271. methane
  133272. rearrangement
  133273. synthetic
  133274. chemistry
  133275. stable
  133276. nitroxides
  133277. synthetic
  133278. developments
  133279. host-guest
  133280. chemistry
  133281. synthetic
  133282. equivalents
  133283. taxol
  133284. system
  133285. examinati
  133286. synthetic
  133287. equivalents
  133288. substituted
  133289. acetylenes
  133290. cycloaddi
  133291. synthetic
  133292. fluorine
  133293. chemistry
  133294. synthetic
  133295. methodology
  133296. based
  133297. n-sulphinyl
  133298. dienophile
  133299. synthetic
  133300. methods
  133301. using
  133302. alpha-heterosubstitu
  133303. organometallics
  133304. synthetic
  133305. modifications
  133306. biologically
  133307. interesting
  133308. natural
  133309. synthetic
  133310. modifications
  133311. erythromycin-a
  133312. macrolactone
  133313. synthetic
  133314. molecular
  133315. knots
  133316. synthetic
  133317. oxidations
  133318. hypochlorites
  133319. synthetic
  133320. oxidations
  133321. hypochlorites
  133322. review
  133323. synthetic
  133324. peptides
  133325. user's
  133326. guide
  133327. synthetic
  133328. perspectives
  133329. photoinduced
  133330. electron
  133331. transfer
  133332. synthetic
  133333. potential
  133334. tertiary
  133335. amine
  133336. catalyzed
  133337. reaction
  133338. synthetic
  133339. potential
  133340. tertiary-amine-catal
  133341. reaction
  133342. synthetic
  133343. procedures
  133344. involving
  133345. organocopper
  133346. reagents
  133347. synthetic
  133348. routes
  133349. 25-disubstituted
  133350. tetrahydrofurans
  133351. synthetic
  133352. routes
  133353. cyclopentanoid-fused
  133354. unnatural
  133355. natur
  133356. synthetic
  133357. routes
  133358. forskolin
  133359. synthetic
  133360. routes
  133361. novel
  133362. homochiral
  133363. sulfenyl
  133364. sulfonium
  133365. synthetic
  133366. routes
  133367. tetrahydrofuran
  133368. tetrahydropyran
  133369. synthetic
  133370. saccharide
  133371. photochemistry
  133372. synthetic
  133373. strategies
  133374. directed
  133375. antitumour
  133376. alkaloids
  133377. synthetic
  133378. strategies
  133379. construction
  133380. 3-pyrrolidinol
  133381. synthetic
  133382. strategy
  133383. construction
  133384. furanohydroph
  133385. synthetic
  133386. studies
  133387. halicondrin
  133388. antitumor
  133389. polyether
  133390. synthetic
  133391. studies
  133392. tandem
  133393. enediyne-mono
  133394. bis-radica
  133395. synthetic
  133396. studies
  133397. active
  133398. forms
  133399. vitamin-d
  133400. their
  133401. synthetic
  133402. studies
  133403. molecular
  133404. recognition
  133405. synthetic
  133406. studies
  133407. pentacyclic
  133408. quassinoids
  133409. synthetic
  133410. studies
  133411. taxol
  133412. fragmentation
  133413. alkoxy
  133414. radic
  133415. synthetic
  133416. studies
  133417. tunicamycin
  133418. antibiotics
  133419. preparation
  133420. synthetic
  133421. studies
  133422. toward
  133423. ciguatoxin
  133424. stereocontrolled
  133425. constru
  133426. synthetic
  133427. studies
  133428. toward
  133429. illudins
  133430. ptaquilosin
  133431. highly
  133432. synthetic
  133433. studies
  133434. towards
  133435. taxol
  133436. analogs
  133437. chemoselective
  133438. cleav
  133439. synthetic
  133440. studies
  133441. cross-coupling
  133442. reaction
  133443. organob
  133444. synthetic
  133445. studies
  133446. natural
  133447. oxazoles
  133448. thiazoles
  133449. synthetic
  133450. study
  133451. antitumor
  133452. antibiotic
  133453. rhizoxin
  133454. using
  133455. synthetic
  133456. transformations
  133457. vinyl
  133458. triflates
  133459. synthetic
  133460. transformations
  133461. using
  133462. arenesulfonyloxy
  133463. groups
  133464. synthetic
  133465. anodic
  133466. substitution
  133467. reactions
  133468. synthetic
  133469. boranes
  133470. synthetic
  133471. dithiane
  133472. group
  133473. synthetic
  133474. 13-dithiane
  133475. group
  133476. 1977-1988
  133477. synthetic
  133478. utility
  133479. alkenylcyclobutenedi
  133480. monoketals
  133481. michael
  133482. synthetic
  133483. utility
  133484. amine
  133485. n-oxides
  133486. synthetic
  133487. utility
  133488. mcpba
  133489. oxidation
  133490. alkyl
  133491. phenyl
  133492. selenid
  133493. synthetic
  133494. utility
  133495. selenium
  133496. carbon
  133497. monoxide
  133498. water
  133499. reaction
  133500. synthetic
  133501. utilization
  133502. highly
  133503. stereoselective
  133504. conjugate
  133505. synthetically
  133506. synthetically
  133507. useful
  133508. extrusion
  133509. reactions
  133510. organic
  133511. sulfur
  133512. synthetically
  133513. useful
  133514. reactions
  133515. epoxides
  133516. synthon
  133517. synthon
  133518. model
  133519. organic
  133520. chemistry
  133521. synthesis
  133522. design
  133523. synthons
  133524. synthons
  133525. parent
  133526. vinyl
  133527. carbene
  133528. complex
  133529. benzann
  133530. synthsis
  133531. synthysis
  133532. synzymes
  133533. system
  133534. system
  133535. systematic
  133536. synthesis
  133537. gangliosides
  133538. toward
  133539. elucidation
  133540. systematization
  133541. systematized
  133542. systems^
  133543. systems
  133544. systems-does
  133545. iesters
  133546. cyclic
  133547. enediol
  133548. phosphoryl
  133549. sytinskii
  133550. sytinskii
  133551. soldatenkov
  133552. conformation
  133553. gamma
  133554. sytnik
  133555. szabo
  133556. szabo
  133557. chiral
  133558. starting
  133559. materials
  133560. reagents
  133561. szabo
  133562. chiral
  133563. starting
  133564. materials
  133565. reagents
  133566. szabolics
  133567. szafran
  133568. szajdzinska
  133569. szajdzinska
  133570. pietek
  133571. gebicki
  133572. scavenging
  133573. hydrat
  133574. szantay
  133575. szantay
  133576. csaba
  133577. dornyei
  133578. gabor
  133579. blasko
  133580. gabor
  133581. morphine
  133582. alkalo
  133583. szeimies
  133584. szele
  133585. szepesi
  133586. szepesi
  133587. gabor
  133588. reverse
  133589. phase
  133590. szeverenyi
  133591. sztaricskai
  133592. szabo
  133593. chiral
  133594. starting
  133595. materials
  133596. reagents
  133597. inclusio@
  133598. kametani
  133599. fukumoto
  133600. methods
  133601. total
  133602. syntheses@
  133603. mukaiyama
  133604. angew
  133605. oxidation
  133606. reduction@
  133607. t-butoxide@
  133608. taddolates@
  133609. takahashi@
  133610. takeya@
  133611. tandem
  133612. tandem
  133613. cyclization
  133614. cycloaddition
  133615. reaction
  133616. rhodium
  133617. carbeni@
  133618. htoush@
  133619. taxonomic
  133620. techniques
  133621. tellurides
  133622. telrazolium@
  133623. terpenoid
  133624. testa
  133625. bernard
  133626. trager
  133627. william
  133628. racemates
  133629. versus
  133630. enantiomers
  133631. tetracoordina@
  133632. tetrahedron
  133633. tetrahedron
  133634. asymmetric
  133635. synthesis
  133636. lignans
  133637. tetrahydropyran
  133638. derivatives
  133639. hexonolactones@
  133640. tetrasubstituted
  133641. furans
  133642. novel
  133643. photocycloaddition
  133644. blumenkopf
  133645. overman
  133646. vinylsil
  133647. cassar
  133648. carbonylation
  133649. organic
  133650. halides
  133651. inclusio
  133652. bailey
  133653. scriven
  133654. heterocycl
  133655. compd
  133656. chemistry
  133657. organosilicon
  133658. compounds
  133659. hogen
  133660. pairing
  133661. effects
  133662. carbanion
  133663. reactions
  133664. fujita
  133665. nishioka
  133666. analysis
  133667. ortho
  133668. effect
  133669. synthesis
  133670. macrocyclic
  133671. lactones
  133672. approaches
  133673. gnewuch
  133674. sosnovsky
  133675. labeled
  133676. alkene
  133677. synthesis
  133678. functionalized
  133679. organosilicon
  133680. acids
  133681. bases
  133682. nakagawa
  133683. oxidation
  133684. indoles
  133685. triplet
  133686. hiraoka
  133687. sugimura
  133688. saito
  133689. kobayashi
  133690. recent
  133691. advances
  133692. olefin
  133693. metathesis
  133694. reaction
  133695. advances
  133696. marks
  133697. accounts
  133698. actinide
  133699. organometall
  133700. bradshaw
  133701. hutchinson
  133702. substituted
  133703. pyrimidine
  133704. kametani
  133705. fukumoto
  133706. accounts
  133707. total
  133708. kametani
  133709. fukumoto
  133710. methods
  133711. total
  133712. syntheses
  133713. kametani
  133714. fukumoto
  133715. syntheses
  133716. quinazolone
  133717. alkaloids
  133718. kametani
  133719. honda
  133720. heterocycl
  133721. appli
  133722. kametani
  133723. total
  133724. synthesis
  133725. isoquinoline
  133726. alkaloids
  133727. koizumi
  133728. tetrahedron
  133729. disproof
  133730. kunieda
  133731. takizawa
  133732. radical
  133733. telomerization
  133734. gilchrist
  133735. moody
  133736. chemistry
  133737. sulfilimines
  133738. tetrahedron
  133739. chemoselectivity
  133740. organometal
  133741. tetrahedron
  133742. chemoselectivity
  133743. organometal
  133744. acids
  133745. bases
  133746. principle
  133747. applicati
  133748. harris
  133749. harris
  133750. synthesis
  133751. polyketide
  133752. aromatic
  133753. mitchell
  133754. organomet
  133755. transition
  133756. metal
  133757. matsuura
  133758. biomimetic
  133759. oxygenation
  133760. tetrahedron
  133761. mukai
  133762. kumagai
  133763. seshimoto
  133764. photochemical
  133765. thermal
  133766. mukaiyama
  133767. asami
  133768. chiral
  133769. mukaiyama
  133770. angew
  133771. oxidation
  133772. reduction
  133773. mukaiyama
  133774. compounds
  133775. mukaiyama
  133776. titanium
  133777. tetrachloride
  133778. organic
  133779. synthesis
  133780. gerasimova
  133781. orlova
  133782. fluor
  133783. synth
  133784. nakai
  133785. mikami
  133786. wittig
  133787. sigmatro
  133788. nishiwaki
  133789. synthesis
  133790. synthesis
  133791. heterocycles
  133792. govindachari
  133793. parthasarathy
  133794. alkaloids
  133795. ancistro
  133796. rosen
  133797. heathcock
  133798. tetrahedron
  133799. synth
  133800. rosenfeld
  133801. honig
  133802. ottolenghi
  133803. hurley
  133804. ebrey
  133805. greenwood
  133806. london
  133807. reactors
  133808. sorenson
  133809. carbocations
  133810. pericyclic
  133811. reactions
  133812. saegusa
  133813. synthesis
  133814. synthesis
  133815. cyclic
  133816. saegusa
  133817. spontaneous
  133818. alternating
  133819. copolymerization
  133820. zwitt
  133821. uchida
  133822. matsumoto
  133823. synthesis
  133824. methods
  133825. wagner
  133826. jauregg
  133827. synthesis
  133828. reactions
  133829. azines
  133830. t-butoxide
  133831. t-butyl
  133832. tabakovic
  133833. taber
  133834. table
  133835. table
  133836. conformational
  133837. energies
  133838. tables
  133839. tabushi
  133840. tacamonine
  133841. tacconi
  133842. tachibana
  133843. tachibana
  133844. akimoto
  133845. kawauchi
  133846. susumu
  133847. yamabe
  133848. tokio
  133849. tachikawa
  133850. tachimori
  133851. tacke
  133852. tacke
  133853. wannagat
  133854. syntheses
  133855. properties
  133856. bioactive
  133857. tackx
  133858. tactical
  133859. tactically
  133860. tactics
  133861. tactics
  133862. organic
  133863. synthesis
  133864. tadao
  133865. tadashi
  133866. taddolate
  133867. tadeusz
  133868. taeboem
  133869. tagaki
  133870. tailor
  133871. tailored
  133872. tailoring
  133873. tailoring
  133874. reactivity
  133875. small
  133876. building
  133877. blocks
  133878. tajima
  133879. takaaki
  133880. takabatake
  133881. takada
  133882. takagi
  133883. takahashi
  133884. takahashi
  133885. kametani
  133886. synthetic
  133887. studies
  133888. mitomycins
  133889. takahashi
  133890. kazuko
  133891. conjugation
  133892. extended
  133893. assemblies
  133894. takahashi
  133895. masaki
  133896. okazaki
  133897. renji
  133898. chemistry
  133899. thionitroso
  133900. takahata
  133901. takahata
  133902. hiroki
  133903. momose
  133904. takefumi
  133905. simple
  133906. indolizidine
  133907. alkaloid
  133908. takahiro
  133909. takaki
  133910. takako
  133911. takaku
  133912. takamizawa
  133913. takamizawa
  133914. matsumoto
  133915. iwata
  133916. makino
  133917. chemistry
  133918. takamuku
  133919. takano
  133920. takao
  133921. takashi
  133922. takata
  133923. takaya
  133924. takayama
  133925. takayama
  133926. mitsuo
  133927. fukai
  133928. toshio
  133929. yoshio
  133930. nomura
  133931. takayuki
  133932. takeda
  133933. takefumi
  133934. takemoto
  133935. takemoto
  133936. kiichi
  133937. miyata
  133938. mikiji
  133939. inclusion
  133940. polymerization
  133941. takeo
  133942. takeru
  133943. takeshi
  133944. takeshita
  133945. takeuchi
  133946. takeya
  133947. takhistov
  133948. takhistov
  133949. rodin
  133950. maksimova
  133951. spectrometry
  133952. taking
  133953. takita
  133954. takizawa
  133955. takken
  133956. takuo
  133957. takuwa
  133958. talib
  133959. tallec
  133960. talyzed
  133961. tamao
  133962. tamao
  133963. kohei
  133964. kobayashi
  133965. kenji
  133966. yoshihiko
  133967. nickel
  133968. mediated
  133969. tamaru
  133970. tamayo
  133971. tamejiro
  133972. tamelen
  133973. tamio
  133974. christoph
  133975. liver
  133976. esterase
  133977. catalyzed
  133978. hydrolysis
  133979. subst
  133980. tamminen
  133981. tamotsu
  133982. tamura
  133983. tamura
  133984. kamimura
  133985. noboru
  133986. displacement
  133987. aliphati
  133988. tamura
  133989. ikeda
  133990. advances
  133991. chemistry
  133992. heteroaromatic
  133993. tanaka
  133994. tanaka
  133995. kazuhiko
  133996. stereoface
  133997. differentiation
  133998. asymmetric
  133999. tanaka
  134000. takita
  134001. pepleomycin
  134002. second
  134003. generation
  134004. bleomyci
  134005. tandem
  134006. tandem
  134007. tandem
  134008. sigmatropic
  134009. rearrangements
  134010. ansamycin
  134011. stereos
  134012. tandem
  134013. alkylation
  134014. trialkyl
  134015. silyl
  134016. dithiane
  134017. preparat
  134018. tandem
  134019. bisalkylation
  134020. trialkylsilyl
  134021. dithiane
  134022. tandem
  134023. conjugate
  134024. addition
  134025. silylcuprate
  134026. benzenesulfeny
  134027. tandem
  134028. rearrangements
  134029. phosphates
  134030. electr
  134031. tandem
  134032. cyclopropanation/cop
  134033. rearrangement
  134034. general
  134035. method
  134036. tandem
  134037. diels
  134038. alder
  134039. double
  134040. intramolecular
  134041. alkyne
  134042. annulati
  134043. tandem
  134044. eneyne
  134045. allene
  134046. radical
  134047. cyclization
  134048. sigmatropic
  134049. tandem
  134050. enyne
  134051. allene
  134052. radical
  134053. cyclization
  134054. sigmatropic
  134055. tandem
  134056. fragmentation
  134057. cyclopropylcarbinyl
  134058. radicals
  134059. tandem
  134060. organic
  134061. reactions
  134062. tandem
  134063. oxidative
  134064. cleavage
  134065. cyclisation
  134066. reactions
  134067. tandem
  134068. oxidative
  134069. cleavage
  134070. cyclization
  134071. reactions
  134072. tandem
  134073. catalyzed
  134074. carbonylation
  134075. intramolecular
  134076. tandem
  134077. radical
  134078. cycloaddition
  134079. remarkable
  134080. silyl
  134081. substituen
  134082. tandem
  134083. radical
  134084. cyclizations
  134085. general
  134086. strategy
  134087. synth
  134088. tandem
  134089. silica
  134090. catalysed
  134091. rearrangements
  134092. subsequent
  134093. tandem
  134094. syntheses
  134095. cyclohexane
  134096. derivatives
  134097. sequential
  134098. tandem
  134099. transesterification
  134100. diastereoselective
  134101. intramolec
  134102. tandem
  134103. transformations
  134104. initiated
  134105. migration
  134106. silyl
  134107. tandem
  134108. transformations
  134109. allenyl
  134110. amines
  134111. indoles
  134112. tandem
  134113. transformations
  134114. alkyl
  134115. allenylmethylaniline
  134116. tandem
  134117. vicinal
  134118. difunctionalization
  134119. beta-addition
  134120. alpha
  134121. taneja
  134122. tanikaga
  134123. tanimoto
  134124. tanko
  134125. tanner
  134126. tanner
  134127. david
  134128. chiral
  134129. aziridines
  134130. their
  134131. synthesis
  134132. tannins
  134133. tanshinone
  134134. tantalum
  134135. phosphinidene
  134136. complexes
  134137. phospha-wittig
  134138. reagent
  134139. tantazole
  134140. tantisewie
  134141. tantisewie
  134142. bamrung
  134143. ruchirawat
  134144. somsak
  134145. alkaloids
  134146. tarak
  134147. tarasevich
  134148. tarasova
  134149. tarbell
  134150. tarbet
  134151. tarburton
  134152. tarburton
  134153. kingsbury
  134154. cromwell
  134155. stereostructural
  134156. target
  134157. targeted
  134158. targeting
  134159. targeting
  134160. minor
  134161. groove
  134162. control
  134163. biological
  134164. targets
  134165. targetted
  134166. tarja
  134167. tarnowski
  134168. tartakovskii
  134169. tartaric
  134170. tarun
  134171. tarunin
  134172. tashiro
  134173. tashiro
  134174. selective
  134175. synthesis
  134176. aromatic
  134177. compounds
  134178. using
  134179. tashma
  134180. tashma
  134181. rachel
  134182. rappoport
  134183. solvent
  134184. induced
  134185. changes
  134186. tashner
  134187. tashtoush
  134188. tasting
  134189. tatar
  134190. tatarinova
  134191. taticchi
  134192. tatlow
  134193. tatlow
  134194. aspects
  134195. organofluorine
  134196. chemistry
  134197. chemistr
  134198. tatsuji
  134199. tatsumi
  134200. tatsunori
  134201. tatsuo
  134202. tatsuta
  134203. tatsuya
  134204. taube
  134205. taube
  134206. henry
  134207. aspects
  134208. binding
  134209. osmium
  134210. ammines
  134211. taurins
  134212. tautomeric
  134213. tautomerism
  134214. tautomers
  134215. tautomycin
  134216. tavares
  134217. taweel
  134218. taxane
  134219. rpene
  134220. synthesis
  134221. strategies
  134222. taxanes
  134223. taxinine
  134224. taxoids
  134225. taxol
  134226. taxol
  134227. taxotere
  134228. discovery
  134229. chemistry
  134230. structure-activit
  134231. taxonomic
  134232. taxonomic
  134233. taxotere
  134234. taxus
  134235. taxusin
  134236. taylorf
  134237. taylor
  134238. turchi
  134239. dipolar
  134240. cyclizations
  134241. taylor
  134242. natural
  134243. products
  134244. containing
  134245. taylor
  134246. stephen
  134247. biosynthetic
  134248. biomimetic
  134249. related
  134250. epoxide
  134251. tbsotf-tea
  134252. tbucu
  134253. tchoubar
  134254. te-bonds
  134255. te-organo
  134256. te-organo
  134257. tellurocarbonates
  134258. te-organotellurocarb
  134259. te-te
  134260. teach
  134261. teaching
  134262. tebben
  134263. technetium
  134264. technetium
  134265. radiopharmaceuticals
  134266. fundamentals
  134267. synthesis
  134268. struc
  134269. technical
  134270. technique
  134271. techniquesQ
  134272. techniques
  134273. technological
  134274. technology
  134275. tedder
  134276. tedder
  134277. walton
  134278. directive
  134279. effects
  134280. phase
  134281. radical
  134282. tedder
  134283. walton
  134284. halogenation
  134285. cycloalkane
  134286. tedder
  134287. walton
  134288. importance
  134289. polarity
  134290. steric
  134291. tedford
  134292. oswald
  134293. stabilization
  134294. transition
  134295. states
  134296. cyclo
  134297. teisseire
  134298. teisseire
  134299. chemistry
  134300. fragrant
  134301. substances
  134302. tel'noi
  134303. tel'noi
  134304. rabinovich
  134305. thermochemistry
  134306. organic
  134307. compou
  134308. teller
  134309. tellur
  134310. telluranes
  134311. telluranes
  134312. synthesis
  134313. structure
  134314. reactivity
  134315. tellurates
  134316. tellurenic
  134317. tellurenic
  134318. acids
  134319. derivatives
  134320. r-te-oh
  134321. telluri
  134322. telluric
  134323. telluride
  134324. tellurides
  134325. tellurides
  134326. tellurinic
  134327. tellurinic
  134328. acids
  134329. derivatives
  134330. organotellurium
  134331. compounds
  134332. tellurium
  134333. tellurium
  134334. compounds
  134335. group
  134336. tellurium
  134337. organic
  134338. synthesis
  134339. tellurium
  134340. reagents
  134341. organic
  134342. synthesis
  134343. recent
  134344. advances
  134345. tellurium-c
  134346. tellurium-containing
  134347. tellurium-containing
  134348. heterocycles
  134349. heteroatoms
  134350. telluriumorganic
  134351. telluriums
  134352. tellurocarbonates
  134353. tellurocyanates
  134354. tellurocyanates
  134355. r-te-ocn
  134356. tellurolates
  134357. tellurolates
  134358. r-te-m
  134359. tellurols
  134360. tellurols
  134361. r-teh
  134362. telluronic
  134363. telluronic
  134364. acids
  134365. derivatives
  134366. tellurophene
  134367. tellurophenes
  134368. tellurophosphates
  134369. tellurous
  134370. telluroxylic
  134371. telomerisation
  134372. telomerization
  134373. telomers
  134374. telrazolium
  134375. teluropyrans
  134376. temarotene
  134377. temparature
  134378. temparature
  134379. effects
  134380. organic
  134381. photochemistry
  134382. tempe
  134383. temperature
  134384. temperature
  134385. solvent
  134386. effect
  134387. nucleophilic
  134388. addition
  134389. endence
  134390. primary
  134391. kinetic
  134392. isotope
  134393. effect
  134394. temperatures
  134395. template
  134396. template
  134397. effects
  134398. distannoxanes
  134399. template
  134400. syntheses
  134401. template-assem
  134402. templated
  134403. templates
  134404. temple
  134405. temple
  134406. triazoles
  134407. chemistry
  134408. heterocyclic
  134409. compound
  134410. templeton
  134411. temporary
  134412. temporary
  134413. magnesium
  134414. aluminum
  134415. connections
  134416. cycloadd
  134417. temporary
  134418. tethering
  134419. strategies
  134420. pyrone
  134421. alkene
  134422. cycload
  134423. ten-membered
  134424. tennant
  134425. tensors
  134426. teplyakov
  134427. teplyakov
  134428. trimerisation
  134429. polycondensation
  134430. aromatic
  134431. terada
  134432. terahara
  134433. terahara
  134434. haneishi
  134435. methylenomycin
  134436. antibiotic
  134437. terashima
  134438. terence
  134439. terent'ev
  134440. terent'ev
  134441. vasil'eva
  134442. synthesis
  134443. reactivity
  134444. terent'eva
  134445. teretifoline
  134446. teriary
  134447. termediates
  134448. terminal
  134449. terminal-unsaturated
  134450. terminally
  134451. terminally
  134452. substituted
  134453. conjugated
  134454. polyenes
  134455. synthesis
  134456. terminated
  134457. terminating
  134458. termination
  134459. terminators
  134460. terminus
  134461. terms
  134462. ternansky
  134463. terocycles
  134464. terpene
  134465. terpenes
  134466. terpenoid
  134467. terpenoid
  134468. terpenoid
  134469. glycosides
  134470. terpenoid
  134471. phytoalexins
  134472. terpenoids
  134473. terpstra
  134474. terrell
  134475. terrier
  134476. terrier
  134477. francois
  134478. nucleophilic
  134479. aromatic
  134480. displacement
  134481. terry
  134482. tert-amino
  134483. tert-amino
  134484. effect
  134485. heterocyclic
  134486. synthesis
  134487. closure
  134488. tert-butyldimethylsi
  134489. tert-butylhydroxyl
  134490. tertiary
  134491. tertiary
  134492. phosphane
  134493. tetrachloromethane
  134494. versatile
  134495. reagent
  134496. tertiary-amine-catal
  134497. teruaki
  134498. teruhisa
  134499. teruo
  134500. terzian
  134501. tessek
  134502. testa
  134503. testa
  134504. bernard
  134505. carrupt
  134506. pierre
  134507. alain
  134508. joseph
  134509. called
  134510. testa
  134511. bernard
  134512. trager
  134513. william
  134514. racemates
  134515. versus
  134516. enantiomers
  134517. testaferri
  134518. testing
  134519. tests
  134520. tests
  134521. purity
  134522. purification
  134523. synthetic
  134524. peptides
  134525. tests
  134526. racemization
  134527. peptide
  134528. construction
  134529. methods
  134530. tethered
  134531. tethering
  134532. tethers
  134533. tetra
  134534. tetra-n-propylammoni
  134535. tetra-nuclear
  134536. tetra-tert-butyltetr
  134537. tetraacetate
  134538. tetraalkyl
  134539. tetraalkylhydrazines
  134540. tetraalkylstannanes
  134541. tetraalkyltin
  134542. tetraallyltin
  134543. tetraaryl
  134544. tetraazamacrocycles
  134545. tetrabenzocyclyne
  134546. tetrabutylammonium
  134547. tetracarbonylferrate
  134548. tetracarbonylhydrido
  134549. tetracarbonylhydrido
  134550. versatile
  134551. tools
  134552. organic
  134553. tetracarbonylhydroco
  134554. tetracarbonylhydroco
  134555. quintessential
  134556. catalyst
  134557. tetrachloride
  134558. tetrachloromethane
  134559. tetracoordina
  134560. tetracoordinate
  134561. tetracoordinated
  134562. tetracyanoethylene
  134563. tetracyanoquinodimet
  134564. tetracycle
  134565. tetracyclic
  134566. tetracyclo
  134567. tetradecane
  134568. tetraenes
  134569. tetraester
  134570. tetraethyl
  134571. tetrafluoride
  134572. tetrafluoroborate
  134573. tetrafluoroborates
  134574. tetrafluroborate
  134575. tetrahalides
  134576. tetrahalomethanes
  134577. tetrahedral
  134578. tetrahedrane
  134579. tetrahedronm
  134580. tetrahedron
  134581. tetrahedron
  134582. tetrahedron
  134583. reviews
  134584. synthetic
  134585. applications
  134586. tetrahedron
  134587. reviews
  134588. selectivity
  134589. synthetic
  134590. tetrahedron
  134591. reviews
  134592. recent
  134593. aspects
  134594. organoselen
  134595. tetrahedron
  134596. reviews
  134597. application
  134598. newer
  134599. organome
  134600. tetrahedron
  134601. asymmetric
  134602. synthesis
  134603. lignans
  134604. tetrahedron
  134605. alpha
  134606. oxoketenes
  134607. acetal
  134608. aceta
  134609. tetrahedron
  134610. glycosidation
  134611. sialic
  134612. okamoto
  134613. tetrahedron
  134614. applications
  134615. liver
  134616. esterases
  134617. tetrahedron
  134618. chemistry
  134619. vinyl
  134620. sulfones
  134621. simpk
  134622. tetrahedron
  134623. asymmetry
  134624. boron
  134625. boranes
  134626. organic
  134627. tetraheterofulvalene
  134628. tetrahydro
  134629. tetrahydro-14-oxazin
  134630. tetrahydrobenz
  134631. tetrahydrobenzofuran
  134632. tetrahydrofuran
  134633. tetrahydrofurans
  134634. tetrahydropyrans
  134635. iodocyclizations
  134636. tetrahydrofurans
  134637. oxonium
  134638. cyclizations
  134639. ketene
  134640. tetrahydroisoquinoli
  134641. tetrahydromevinic
  134642. tetrahydroprotoberbe
  134643. tetrahydropyran
  134644. tetrahydropyran
  134645. derivatives
  134646. hexonolactones
  134647. tetrahydropyrans
  134648. tetrahydropyranyl
  134649. tetrahydropyridines
  134650. tetrahydropyridinium
  134651. tetrahydroquinoxalin
  134652. tetrahydrothiophenes
  134653. tetrahymanol
  134654. tetrahymena
  134655. tetrakis
  134656. tetralones
  134657. tetramer
  134658. tetramethyl
  134659. tetramethylazodicarb
  134660. tetramethylene
  134661. tetramethylethylened
  134662. tetramethyloctadehyd
  134663. tetramic
  134664. tetraorganosilanes
  134665. tetraorganosulfurane
  134666. tetraorganotellurium
  134667. tetraorganotellurium
  134668. alkylidenediorganote
  134669. compounds
  134670. tetraoxide
  134671. tetrapeptide
  134672. tetraphenyl
  134673. tetraphenylene
  134674. tetrapropylv
  134675. tetrapropylammonium
  134676. tetrapropylammonium
  134677. perruthenate
  134678. catalytic
  134679. tetrapropylammonium
  134680. perruthenate
  134681. catalytic
  134682. tetraselenafulvalene
  134683. tetrasubstituted
  134684. tetrasubstituted
  134685. furans
  134686. novel
  134687. photocycloaddition
  134688. tetrasulfides
  134689. tetrathiafulvalenes
  134690. tetrathiafulvalenes
  134691. building-blocks
  134692. supramolecular
  134693. tetrathianes
  134694. tetrathiofulvalene
  134695. tetrazines
  134696. tetrazocines
  134697. tetrazole
  134698. tetrazoles
  134699. tetronomycin
  134700. tetroxide
  134701. tetroxides
  134702. tetsuo
  134703. tetsuro
  134704. tetsuya
  134705. teuber
  134706. teucrium
  134707. texaphyrins
  134708. texaphyrins
  134709. synthesis
  134710. applications
  134711. textbook
  134712. synthesis
  134713. acetylenes
  134714. thailand
  134715. thallium
  134716. thallium
  134717. organic
  134718. synthesis
  134719. thatcher
  134720. thayer
  134721. hydrogen
  134722. shift
  134723. common
  134724. vehicle
  134725. disappearance@
  134726. reaction
  134727. group
  134728. group
  134729. enolates@
  134730. application
  134731. thermolytic
  134732. reactions
  134733. synthesis
  134734. baeyer-villiger
  134735. oxidation
  134736. ketones
  134737. catalyzed
  134738. nickel@
  134739. biocatalytic
  134740. approach
  134741. preparation
  134742. enantiomeric@
  134743. catalyzed
  134744. nucleophilic
  134745. addition
  134746. aldehydes
  134747. electrop@
  134748. chemistry
  134749. 4-azaazulenes
  134750. chemistry
  134751. azaphosphorins@
  134752. chemistry
  134753. diimine@
  134754. chemistry
  134755. ketenes
  134756. allenes
  134757. related
  134758. compounds@
  134759. chemistry
  134760. pyrroloindoles@
  134761. chemistry
  134762. fullerenes
  134763. overview@
  134764. chemistry
  134765. vicinal
  134766. polyketones@
  134767. clemmensen
  134768. reduction
  134769. elmore
  134770. martin
  134771. organic
  134772. reactions
  134773. elimination
  134774. sulfoxide
  134775. elimination
  134776. related
  134777. therm@
  134778. design
  134779. application
  134780. radical
  134781. chain
  134782. reactions
  134783. cycloaddition
  134784. azodicarboxylates
  134785. cyclic
  134786. vinyl
  134787. 9-fluorenylmethy
  134788. oxycarbonyl
  134789. family
  134790. base-sensitive
  134791. aceto
  134792. acetic
  134793. ester
  134794. condensation
  134795. certain
  134796. related
  134797. acetoacetic
  134798. ester
  134799. condensation
  134800. certain
  134801. related
  134802. react
  134803. promoted
  134804. decomposition
  134805. alpha-diazoketones
  134806. acylation
  134807. aromatic
  134808. compounds
  134809. friedel
  134810. crafts
  134811. acylation
  134812. ketones
  134813. diketones
  134814. aldehydes
  134815. acyloin
  134816. condensation
  134817. acyloin
  134818. condensation
  134819. jordan
  134820. bloomfield
  134821. dennis
  134822. owsley
  134823. acyloins
  134824. acyloins
  134825. mcelvain
  134826. organic
  134827. reactions
  134828. volume
  134829. addition
  134830. trimethylsilyl
  134831. allylboronates
  134832. imines
  134833. addition
  134834. organometallic
  134835. reagents
  134836. oxabicyclo
  134837. adventure
  134838. playground
  134839. aldol
  134840. addition
  134841. reaction
  134842. aldol
  134843. condensation
  134844. aldol
  134845. condensation
  134846. arnold
  134847. nielsen
  134848. william
  134849. houlih
  134850. aldol
  134851. reaction
  134852. general
  134853. catalysis
  134854. aldol
  134855. reaction
  134856. group
  134857. group
  134858. enolates
  134859. aldol
  134860. reaction
  134861. group
  134862. enolates
  134863. aldol
  134864. reaction
  134865. transition
  134866. metal
  134867. enolates
  134868. aliphatic
  134869. friedel-crafts
  134870. reaction
  134871. alkylation
  134872. aromatic
  134873. compounds
  134874. friedel-crafts
  134875. alkylation
  134876. esters
  134877. nitriles
  134878. allylcobalt
  134879. system
  134880. aluminum
  134881. amalgam
  134882. reduction
  134883. nitroalkanols
  134884. promoted
  134885. amination
  134886. heterocyclic
  134887. bases
  134888. alkali
  134889. amides
  134890. amination
  134891. heterocyclic
  134892. bases
  134893. alkali
  134894. amides
  134895. revie
  134896. anomeric
  134897. effect
  134898. associated
  134899. stereoelectronic
  134900. effects
  134901. anomeric
  134902. effect
  134903. related
  134904. stereoelectronic
  134905. effects
  134906. phase
  134907. heterogeneous-cataly
  134908. hydrogenation
  134909. carbony
  134910. app-klingemann
  134911. reaction
  134912. applicability
  134913. asymmetric
  134914. homogeneous
  134915. catalytic
  134916. hydrog
  134917. application
  134918. friedlander
  134919. fischer
  134920. methodologies
  134921. application
  134922. low-valent
  134923. titanium
  134924. reagents
  134925. organic
  134926. application
  134927. thermolytic
  134928. reactions
  134929. synthesis
  134930. arndt
  134931. eistert
  134932. reaction
  134933. bachmann
  134934. struve
  134935. organ
  134936. arndt-eistert
  134937. reaction
  134938. asymmetric
  134939. michael
  134940. addit
  134941. reaction
  134942. using
  134943. chiral
  134944. imines
  134945. asymmetric
  134946. michael
  134947. reaction
  134948. using
  134949. chiral
  134950. imines
  134951. under
  134952. asymmetric
  134953. synthesis
  134954. alkaloids
  134955. alpha-alkylation
  134956. asymmetric
  134957. synthesis
  134958. quinocarcin
  134959. 13-dipolar
  134960. cyclo
  134961. asymmetric
  134962. ullmann
  134963. reaction
  134964. application
  134965. first
  134966. methane
  134967. rearrangement
  134968. unsaturated
  134969. oximes
  134970. wittig
  134971. reaction
  134972. heterocyclic
  134973. synthesis
  134974. review
  134975. aza-wittig
  134976. reaction
  134977. heterocyclic
  134978. synthesis
  134979. azetidines
  134980. recent
  134981. synthetic
  134982. developments
  134983. azide
  134984. method
  134985. peptide
  134986. synthesis
  134987. scope
  134988. limitati
  134989. azinyl-azinylid
  134990. tautomerism
  134991. azinylmethanes
  134992. baeyer-villiger
  134993. oxidation
  134994. aldehydes
  134995. ketones
  134996. baeyer-villiger
  134997. oxidation
  134998. ketones
  134999. aldehydes
  135000. baeyer-villiger
  135001. oxidation
  135002. ketones
  135003. catalyzed
  135004. nickel
  135005. baeyer-villiger
  135006. reactions
  135007. barbier
  135008. reaction
  135009. related
  135010. processes
  135011. barbier
  135012. reaction
  135013. related
  135014. one-step
  135015. processes
  135016. barbier
  135017. reaction-a
  135018. alternative
  135019. syntheses
  135020. promoted
  135021. rearrangements
  135022. quaternary
  135023. ammonium
  135024. base-promoted
  135025. rearrangements
  135026. quaternary
  135027. ammonium
  135028. battle
  135029. calicheamicin
  135030. gamma1
  135031. rings
  135032. taxol
  135033. photocycloaddition
  135034. beckmann
  135035. related
  135036. reactions
  135037. beckmann
  135038. reactions
  135039. rearrangements
  135040. elimination
  135041. additions
  135042. beckmann
  135043. rearrangement
  135044. beckmann
  135045. rearrangement
  135046. donaruma
  135047. walter
  135048. heldt
  135049. beirut
  135050. reaction
  135051. benzoin
  135052. related
  135053. anion
  135054. equivalent
  135055. reactions
  135056. bimolecular
  135057. aliphatic
  135058. mannich
  135059. related
  135060. reactions
  135061. bimolecular
  135062. aromatic
  135063. friedel-crafts
  135064. reaction
  135065. bimolecular
  135066. aromatic
  135067. mannich
  135068. reaction
  135069. biocatalytic
  135070. approach
  135071. preparation
  135072. enantiomeric
  135073. biochemical
  135074. reactions
  135075. organometallics
  135076. enzymes
  135077. biological
  135078. activity
  135079. selenium
  135080. sulfide
  135081. biosynthesis
  135082. synthesis
  135083. shikimic
  135084. chorismic
  135085. biosynthesis
  135086. plant
  135087. alkaloids
  135088. nitrogenous
  135089. microbia
  135090. biosynthesis
  135091. tropane
  135092. alkaloids
  135093. birch
  135094. reduction
  135095. aromatic
  135096. compounds
  135097. bonding
  135098. properties
  135099. cyclopropane
  135100. their
  135101. chemical
  135102. boron
  135103. approach
  135104. asymmetric
  135105. synthesis
  135106. borylation
  135107. aromatic
  135108. compounds
  135109. dehalogenation
  135110. produ
  135111. bryostatins
  135112. bucherer
  135113. reaction
  135114. bucherer
  135115. reaction
  135116. nathan
  135117. drake
  135118. organic
  135119. reactions
  135120. volum
  135121. apman
  135122. rearrangement
  135123. calicheamicins
  135124. cannizzaro
  135125. reaction
  135126. cannizzaro
  135127. reaction
  135128. geissman
  135129. organic
  135130. reactions
  135131. volum
  135132. captodative
  135133. effect
  135134. carboxylic
  135135. group
  135136. effective
  135137. director
  135138. ortho
  135139. catalyzed
  135140. nucleophilic
  135141. addition
  135142. aldehydes
  135143. electrop
  135144. mistry
  135145. pyrazolidinones
  135146. champagne
  135147. route
  135148. avermectins
  135149. milbemycins
  135150. chapman
  135151. rearrangement
  135152. schulenberg
  135153. archer
  135154. organ
  135155. chemical
  135156. properties
  135157. buckminsterfullerene
  135158. chemical
  135159. synthesis
  135160. oligonucleotides
  135161. chemical
  135162. synthesis
  135163. peptides
  135164. chemistry
  135165. biochemistry
  135166. n-substituted
  135167. porphyrins
  135168. chemistry
  135169. derivatives
  135170. supplement
  135171. chemistry
  135172. 12-carbonyl
  135173. transposition
  135174. chemistry
  135175. 12-dithiins
  135176. chemistry
  135177. dioximes
  135178. brief
  135179. review
  135180. chemistry
  135181. thiazolinone
  135182. hydroxy
  135183. thiazole
  135184. chemistry
  135185. 13-dioximes
  135186. chemistry
  135187. 14-dioxene
  135188. 23-dihydro-14-dioxin
  135189. chemistry
  135190. orthocyclophanes
  135191. classes
  135192. ionophor
  135193. chemistry
  135194. oxazolines
  135195. present
  135196. chemistry
  135197. 2-oxazolines
  135198. 1985-present
  135199. chemistry
  135200. 4-azaazulenes
  135201. chemistry
  135202. 4-azaazulenes
  135203. chemistry
  135204. dihydro
  135205. oxazoles
  135206. chemistry
  135207. 4h-13-dithiins
  135208. chemistry
  135209. oxodihydroisoxazoles
  135210. photolysis
  135211. chemistry
  135212. oxodihydroisoxazoles
  135213. annelated
  135214. pyrimidi
  135215. chemistry
  135216. acetylcyclopropane
  135217. chemistry
  135218. vatives
  135219. supplement
  135220. chemistry
  135221. cyanides
  135222. chemistry
  135223. halides
  135224. chemistry
  135225. tellurides
  135226. generation
  135227. trapping
  135228. chemistry
  135229. alkanes
  135230. cycloalkanes
  135231. chemistry
  135232. alkenes
  135233. chemistry
  135234. allyl
  135235. crotyl
  135236. grignard
  135237. reagents
  135238. chemistry
  135239. alpha
  135240. ketones
  135241. related
  135242. species
  135243. chemistry
  135244. alpha-halo
  135245. ketones
  135246. alpha-halo
  135247. aldehydes
  135248. chemistry
  135249. amides
  135250. chemistry
  135251. amidines
  135252. imidates
  135253. chemistry
  135254. amino
  135255. nitroso
  135256. nitro
  135257. compounds
  135258. their
  135259. chemistry
  135260. antitumor
  135261. antibiotics
  135262. chemistry
  135263. azadirachtin
  135264. chemistry
  135265. azaphosphorins
  135266. chemistry
  135267. benzazetes
  135268. chemistry
  135269. boron
  135270. analogs
  135271. biomolecules
  135272. tetrahedron
  135273. chemistry
  135274. carbenoids
  135275. other
  135276. thermolabile
  135277. organolit
  135278. chemistry
  135279. carboxylic
  135280. derivatives
  135281. supplement
  135282. chemistry
  135283. carboxylic
  135284. acids
  135285. esters
  135286. chemistry
  135287. chloral
  135288. chemistry
  135289. conjugated
  135290. compounds
  135291. chemistry
  135292. cyanates
  135293. their
  135294. derivatives
  135295. chemistry
  135296. cyanotrimethylsilane
  135297. chemistry
  135298. cyclobutendione
  135299. reactions
  135300. allyl
  135301. alhenyl
  135302. chemistry
  135303. cycloocta
  135304. dipyridine
  135305. chemistry
  135306. cyclopro
  135307. ylmethyl
  135308. related
  135309. radicals
  135310. chemistry
  135311. cyclopropylmethyl
  135312. related
  135313. radicals
  135314. chemistry
  135315. cymantrene
  135316. chemistry
  135317. ddathf
  135318. 510-dideaza-5678-tet
  135319. antitum
  135320. chemistry
  135321. diazonium
  135322. diazo
  135323. groups
  135324. chemistry
  135325. dichloromethyleneamm
  135326. salts
  135327. phosgenammonium
  135328. chemistry
  135329. diimine
  135330. chemistry
  135331. diphosphenes
  135332. their
  135333. heavy
  135334. congeners
  135335. chemistry
  135336. disulfides
  135337. chemistry
  135338. double-bonded
  135339. functional
  135340. groups
  135341. chemistry
  135342. double-bonded
  135343. functional
  135344. groups
  135345. supplement
  135346. chemistry
  135347. enaminonitriles
  135348. versatile
  135349. reagents
  135350. chemistry
  135351. ethers
  135352. chemistry
  135353. enols
  135354. chemistry
  135355. enones
  135356. chemistry
  135357. ethers
  135358. crown
  135359. ethers
  135360. hydroxyl
  135361. groups
  135362. chemistry
  135363. formamide
  135364. acetals
  135365. chemistry
  135366. gibberellins
  135367. overview
  135368. chemistry
  135369. halides
  135370. pseudohalides
  135371. azides
  135372. supplement
  135373. chemistry
  135374. higher
  135375. order
  135376. organocuprates
  135377. chemistry
  135378. hydroxamic
  135379. acids
  135380. n-hydroxyimides
  135381. chemistry
  135382. hydroxyl
  135383. ether
  135384. peroxide
  135385. groups
  135386. suppleme
  135387. chemistry
  135388. icarbonylcyclopentad
  135389. complexes
  135390. progres
  135391. chemistry
  135392. iminoboranes
  135393. chemistry
  135394. iodine
  135395. azide
  135396. chemistry
  135397. isatoic
  135398. anhydride
  135399. chemistry
  135400. ketenes
  135401. allenes
  135402. related
  135403. compounds
  135404. chemistry
  135405. lactams
  135406. chemistry
  135407. macrocyclic
  135408. ligand
  135409. lexes
  135410. chemistry
  135411. mixed
  135412. rganosulfur-silicon
  135413. compounds
  135414. chemistry
  135415. molten
  135416. acetamide
  135417. acetamide
  135418. complexes
  135419. chemistry
  135420. n-pentenyl
  135421. glycosides
  135422. synthetic
  135423. theoretical
  135424. chemistry
  135425. nitrile
  135426. sulfides
  135427. dipolar
  135428. cycloaddition
  135429. chemistry
  135430. nitrile
  135431. sulphides
  135432. chemistry
  135433. organic
  135434. selenium
  135435. tellurium
  135436. compounds
  135437. chemistry
  135438. organic
  135439. selenium
  135440. tellurium
  135441. compounds
  135442. chemistry
  135443. organophosphorus
  135444. compounds
  135445. chemistry
  135446. organophosphorus
  135447. compounds
  135448. phosphine
  135449. oxides
  135450. chemistry
  135451. perfluoroalkyl-subst
  135452. dicyanoethylenes
  135453. chemistry
  135454. peroxides
  135455. chemistry
  135456. peroxonium
  135457. dioxygen
  135458. ylides
  135459. chemistry
  135460. phosgene
  135461. chemistry
  135462. polyfunctional
  135463. organozinc
  135464. copper
  135465. reagen
  135466. chemistry
  135467. pyrazolidinones
  135468. review
  135469. chemistry
  135470. pyrroloindoles
  135471. chemistry
  135472. sulfenamides
  135473. chemistry
  135474. sulfenic
  135475. acids
  135476. chemistry
  135477. sulfenic
  135478. acids
  135479. their
  135480. derivatives
  135481. chemistry
  135482. sulfilimines
  135483. chemistry
  135484. sulfinic
  135485. acids
  135486. esters
  135487. their
  135488. derivatives
  135489. chemistry
  135490. sulfones
  135491. sulfoxides
  135492. chemistry
  135493. sulfonic
  135494. acids
  135495. esters
  135496. their
  135497. derivatives
  135498. chemistry
  135499. sulfur-containing
  135500. functional
  135501. groups
  135502. chemistry
  135503. superoxide
  135504. chemistry
  135505. sydnones
  135506. chemistry
  135507. amidines
  135508. imidates
  135509. chemistry
  135510. amino
  135511. group
  135512. chemistry
  135513. azido
  135514. group
  135515. chemistry
  135516. carbon-carbon
  135517. triple
  135518. chemistry
  135519. carbon-halogen
  135520. chemistry
  135521. carbon-nitrogen
  135522. double
  135523. chemistry
  135524. carbonyl
  135525. group
  135526. chemistry
  135527. cyano
  135528. group
  135529. chemistry
  135530. cyclopropyl
  135531. group
  135532. chemistry
  135533. ether
  135534. linkage
  135535. chemistry
  135536. fullerenes
  135537. overview
  135538. chemistry
  135539. hydrazo
  135540. azoxy
  135541. groups
  135542. chemistry
  135543. hydroxyl
  135544. group
  135545. chemistry
  135546. metal-carbon
  135547. chemistry
  135548. metal-carbon
  135549. carbon-carbon
  135550. chemistry
  135551. metal-carbon
  135552. nature
  135553. cleavag
  135554. chemistry
  135555. metal-carbon
  135556. organometa
  135557. chemistry
  135558. metal-carbon
  135559. volume
  135560. structur
  135561. chemistry
  135562. nitro
  135563. nitroso
  135564. groups
  135565. chemistry
  135566. quinonoid
  135567. compounds
  135568. chemistry
  135569. sulfonium
  135570. group
  135571. chemistry
  135572. thiol
  135573. group
  135574. chemistry
  135575. thiohydroxamic
  135576. acids
  135577. chemistry
  135578. thioketenes
  135579. chemistry
  135580. thionitroso
  135581. compounds
  135582. chemistry
  135583. thioph
  135584. salts
  135585. thiophenium
  135586. ylides
  135587. chemistry
  135588. triple-bonded
  135589. functional
  135590. groups
  135591. supplement
  135592. chemistry
  135593. unsaturated
  135594. nitrogen-heterocycli
  135595. compounds
  135596. chemistry
  135597. vicinal
  135598. polyketones
  135599. chemistry
  135600. vinyl
  135601. nitroxides
  135602. chemistry
  135603. vinyl
  135604. sulfones
  135605. chemistry
  135606. vinyl
  135607. sulfones
  135608. brief
  135609. review
  135610. article
  135611. chemistry
  135612. vitamin
  135613. vision
  135614. chiral
  135615. auxiliary
  135616. asymmetric
  135617. synthesi
  135618. chiral
  135619. source
  135620. enantioselective
  135621. catalysts
  135622. claisen
  135623. rearrangements
  135624. claisen
  135625. rearrangements
  135626. rhoads
  135627. claisen
  135628. rearrangement
  135629. claisen
  135630. rearrangement
  135631. stanley
  135632. tarbell
  135633. organic
  135634. reaction
  135635. claisen
  135636. rearrangement
  135637. claisen
  135638. rearrangement
  135639. organic
  135640. synthesis
  135641. claisen
  135642. rearrangement
  135643. propargyloxycoumarin
  135644. formatio
  135645. classical
  135646. permangana
  135647. still
  135648. novel
  135649. oxidant
  135650. cleavage
  135651. enolizable
  135652. ketones
  135653. sodium
  135654. amide
  135655. cleavage
  135656. non-enolizable
  135657. ketones
  135658. sodium
  135659. amide
  135660. clemmensen
  135661. reduction
  135662. clemmensen
  135663. reduction
  135664. elmore
  135665. martin
  135666. organic
  135667. reactions
  135668. combination
  135669. hydrogen
  135670. fluoride
  135671. organic
  135672. bases
  135673. composition
  135674. grignard
  135675. compounds
  135676. ether
  135677. solvents
  135678. concept
  135679. aromaticity
  135680. heterocyclic
  135681. chemistry
  135682. concept
  135683. strain
  135684. organic
  135685. chemistry
  135686. configurational
  135687. stability
  135688. chiral
  135689. lithio
  135690. amino
  135691. carba
  135692. conformation
  135693. hydroxylamines
  135694. conformational
  135695. analysis
  135696. 14-cyclohexadienes
  135697. 14-dihydro
  135698. conformational
  135699. analysis
  135700. cyclohexenes
  135701. cyclohexadienes
  135702. conformational
  135703. analysis
  135704. heterocyclic
  135705. compounds
  135706. conformational
  135707. analysis
  135708. organoelemental
  135709. nomet
  135710. consequences
  135711. strain
  135712. structure
  135713. aliphatic
  135714. contrasting
  135715. behavior
  135716. oxirane
  135717. oxetane
  135718. cationic
  135719. conversion
  135720. carbohydrate
  135721. derivatives
  135722. functiona
  135723. coordination
  135724. chemistry
  135725. organometallic
  135726. chemistry
  135727. elimination
  135728. sulfoxide
  135729. elimination
  135730. related
  135731. therm
  135732. coupling
  135733. diazonium
  135734. salts
  135735. alipbatic
  135736. carbon
  135737. atoms
  135738. coupling
  135739. diazonium
  135740. salts
  135741. aliphatic
  135742. carbon
  135743. atoms
  135744. cross
  135745. coupling
  135746. reactions
  135747. organic
  135748. halides
  135749. organic
  135750. current
  135751. dynamic
  135752. change
  135753. within
  135754. cyclooctatetraenes
  135755. curtius
  135756. reaction
  135757. curtius
  135758. reaction
  135759. peter
  135760. smith
  135761. organic
  135762. reactions
  135763. volum
  135764. cycloaddition
  135765. approach
  135766. alpha-hydroxy
  135767. carbonyls
  135768. cycloaddition
  135769. allyl
  135770. cations
  135771. dienes
  135772. general
  135773. cycloaddition
  135774. allyl
  135775. cations
  135776. 13-dienes
  135777. general
  135778. cyclobutadiene
  135779. problem
  135780. cyclopropyl
  135781. radical
  135782. dakin-west
  135783. reaction
  135784. darzens
  135785. glycidic
  135786. ester
  135787. condensation
  135788. darzens
  135789. glycidic
  135790. ester
  135791. condensation
  135792. melvin
  135793. newman
  135794. decomposition
  135795. alkyl
  135796. nitrites
  135797. reactions
  135798. demjanov
  135799. tiffeneau-demjanov
  135800. nsions
  135801. description
  135802. stereochemistry
  135803. design
  135804. application
  135805. radical
  135806. chain
  135807. reactions
  135808. design
  135809. construction
  135810. synthetic
  135811. protein
  135812. mimics
  135813. design
  135814. synthesis
  135815. immune
  135816. regulatory
  135817. agents
  135818. targets
  135819. design
  135820. chemoselective
  135821. reduction
  135822. catalyst
  135823. development
  135824. concepts
  135825. chiral
  135826. discrimination
  135827. development
  135828. organometallic
  135829. methodologies
  135830. methane
  135831. oxa-di
  135832. methane
  135833. rearrangements
  135834. methane
  135835. rearrangement
  135836. methane
  135837. rearrangement
  135838. systems
  135839. simple
  135840. vinyl
  135841. diagnosis
  135842. concerted
  135843. organic
  135844. mechanisms
  135845. dieckmann
  135846. condensation
  135847. dieckmann
  135848. condensation
  135849. schaefer
  135850. jordan
  135851. diels
  135852. alder
  135853. reaction
  135854. ethylenic
  135855. acetylenic
  135856. dienophile
  135857. diels
  135858. alder
  135859. reaction
  135860. quinones
  135861. other
  135862. cyclenones
  135863. lewis
  135864. diels
  135865. alder
  135866. reaction
  135867. maleic
  135868. anhydride
  135869. milton
  135870. diels-alder
  135871. reaction
  135872. ethylenic
  135873. acetylenic
  135874. dienophile
  135875. diels-alder
  135876. reaction
  135877. quinones
  135878. other
  135879. cyclenones
  135880. diels-alder
  135881. reaction
  135882. maleic
  135883. anhydride
  135884. diradical
  135885. mechanism
  135886. 13-dipolar
  135887. cycloadditions
  135888. direct
  135889. synthesis
  135890. non-transition-metal
  135891. organo
  135892. derivati
  135893. directed
  135894. aldol
  135895. reaction
  135896. directed
  135897. ortho
  135898. metalation
  135899. reaction
  135900. methodology
  135901. applicati
  135902. directed
  135903. pauson
  135904. khand
  135905. reaction
  135906. alkenes
  135907. alkynes
  135908. directed
  135909. synthesis
  135910. biaryl
  135911. compounds
  135912. modern
  135913. concepts
  135914. discovery
  135915. crown
  135916. ethers
  135917. diverse
  135918. reactivity
  135919. benzothiazol
  135920. ylthio
  135921. benzotriazol
  135922. diyne
  135923. reaction
  135924. 17-diynes
  135925. transition
  135926. dna-esperamicin
  135927. complex
  135928. model
  135929. based
  135930. solvated
  135931. double
  135932. carbonylation
  135933. diiodomethane
  135934. catalysed
  135935. rhodi
  135936. effect
  135937. fluorination
  135938. enolates
  135939. enolate
  135940. equivalen
  135941. effect
  135942. fluorine
  135943. substituent
  135944. selected
  135945. properti
  135946. effect
  135947. cleavage
  135948. potency
  135949. tethering
  135950. simple
  135951. diels-alder
  135952. reaction
  135953. quinones
  135954. other
  135955. cyclenones@
  135956. reaction@
  135957. favorskii
  135958. rearrangement
  135959. haloketones@
  135960. first
  135961. example
  135962. transition
  135963. metal
  135964. catalyzed
  135965. thioformylat@
  135966. friedel-crafts
  135967. acylation
  135968. alkenes@
  135969. generation
  135970. nitrogen
  135971. radicals
  135972. their
  135973. cyclizations
  135974. dole-23-quinodimetha
  135975. strategy
  135976. synthesis
  135977. intramolecular
  135978. trapping
  135979. reaction
  135980. useful
  135981. kinetics
  135982. ylide
  135983. forming
  135984. reaction
  135985. between
  135986. triplet
  135987. diphe@
  135988. mechanism
  135989. organocuprate
  135990. 14-addition
  135991. reactions
  135992. nature
  135993. radicals
  135994. involved
  135995. grignard
  135996. reagent
  135997. formatio@
  135998. orgin
  135999. regioselectivity
  136000. allenyllithium
  136001. reagent@
  136002. oxenoid
  136003. character
  136004. metalated
  136005. hydroperoxides
  136006. persulfate
  136007. oxidation
  136008. phenols
  136009. arylamines
  136010. pictet
  136011. spengler
  136012. synthesis
  136013. tetrahydroisoquinoli
  136014. acetic
  136015. esters
  136016. alkenes
  136017. alkynes
  136018. hete@
  136019. reaction
  136020. reaction
  136021. louis
  136022. fieser
  136023. organic
  136024. reactions
  136025. volume
  136026. electrochemistry
  136027. transition
  136028. metal
  136029. complexes
  136030. electrocyclic
  136031. opening
  136032. fluorinated
  136033. cyclobutene
  136034. electronic
  136035. structure
  136036. stereochemistry
  136037. simple
  136038. carbo
  136039. electrophilic
  136040. amination
  136041. organolithiums
  136042. methyllit
  136043. electrophilic
  136044. substitution
  136045. allylsilanes
  136046. vinylsila
  136047. elusive
  136048. zirconium
  136049. reaction
  136050. energetic
  136051. advantage
  136052. 5-exo
  136053. versus
  136054. 6-endo
  136055. epoxide
  136056. openi
  136057. ether
  136058. synthesis
  136059. polyenes
  136060. enol-keto
  136061. trigger
  136062. initiating
  136063. arene
  136064. diradical
  136065. formatio
  136066. eschenmoser
  136067. coupling
  136068. reactions
  136069. ester
  136070. enolate
  136071. imine
  136072. condensation
  136073. route
  136074. lactams
  136075. ester
  136076. enolate-imine
  136077. condensation
  136078. route
  136079. lactams
  136080. evolution
  136081. higher
  136082. order
  136083. cyanocup
  136084. fascinating
  136085. organometallic
  136086. chemistry
  136087. phosphaalkynes
  136088. favorskii
  136089. rearrangement
  136090. favorskii
  136091. rearrangement
  136092. haloketones
  136093. first
  136094. asymmetric
  136095. synthesis
  136096. lycorine
  136097. alkaloid
  136098. total
  136099. first
  136100. enantioselective
  136101. synthesis
  136102. chemotactic
  136103. first
  136104. examples
  136105. carbon
  136106. monoxide
  136107. trapping
  136108. manganes
  136109. first
  136110. heterobimetallic
  136111. multifunctional
  136112. asymmetric
  136113. cataly
  136114. first
  136115. isolable
  136116. dithiirane
  136117. oxidation
  136118. dithietane
  136119. first
  136120. total
  136121. syntheses
  136122. taxol
  136123. fluorinated
  136124. natural-products
  136125. fluorine
  136126. cation-stabilizing
  136127. auxiliary
  136128. biomi
  136129. folding
  136130. squalene
  136131. problem
  136132. results
  136133. formation
  136134. bonds
  136135. alpha-halogeno
  136136. formation
  136137. cyclic
  136138. ketones
  136139. intramolecular
  136140. acylation
  136141. formation
  136142. cyclic
  136143. ketones
  136144. intramolecular
  136145. acylation
  136146. formation
  136147. distannanes
  136148. hydrides
  136149. friedel
  136150. crafts
  136151. reaction
  136152. aliphatic
  136153. dibasic
  136154. friedel
  136155. crats
  136156. reaction
  136157. iphatic
  136158. dibasic
  136159. friedel-crafts
  136160. acylation
  136161. alkenes
  136162. friedlander
  136163. synthesis
  136164. quinolines
  136165. fries
  136166. reaction
  136167. fries
  136168. reaction
  136169. blatt
  136170. organic
  136171. reactions
  136172. volume
  136173. fujimoto-belleau
  136174. reaction
  136175. fullerenes
  136176. allotropic
  136177. forms
  136178. carbon
  136179. molecular
  136180. fullerenes
  136181. horizons
  136182. chemistry
  136183. physics
  136184. functional
  136185. group
  136186. selectivity
  136187. complex
  136188. hydride
  136189. reducing
  136190. functionalization
  136191. oligon
  136192. cleotides
  136193. phosphoramidit
  136194. gabriel
  136195. reaction
  136196. anomalies
  136197. revisited
  136198. gabriel
  136199. synthesis
  136200. primary
  136201. amines
  136202. gamma
  136203. alkylation
  136204. gamma
  136205. arylation
  136206. dianions
  136207. gamma-alkylation
  136208. gamma-arylation
  136209. dianons
  136210. beta-
  136211. gattermann
  136212. reaction
  136213. nathan
  136214. crounse
  136215. organic
  136216. reacti
  136217. gattermann
  136218. synthesis
  136219. aldehydes
  136220. gattermann-koch
  136221. reaction
  136222. gauche
  136223. effect
  136224. stereochemical
  136225. consequences
  136226. adjace
  136227. generation
  136228. double
  136229. bonds
  136230. specific
  136231. geometry
  136232. regio
  136233. generation
  136234. nitrogen
  136235. radicals
  136236. their
  136237. cyclizations
  136238. halogen
  136239. metal
  136240. interconversion
  136241. reaction
  136242. organolithiu
  136243. halogen-metal
  136244. interconversion
  136245. reaction
  136246. organolithiu
  136247. helicenes
  136248. henry
  136249. nitroaldol
  136250. reaction
  136251. hetero
  136252. rearrangement
  136253. organic
  136254. synthesis
  136255. hetero-cope
  136256. rearrangement
  136257. organic
  136258. synthesis
  136259. histrionicotoxins
  136260. ynthesis
  136261. 1-azaspiro
  136262. undecane
  136263. hoesch
  136264. synthesis
  136265. hoesch
  136266. synthesis
  136267. spoerri
  136268. adrien
  136269. dubois
  136270. hofmann
  136271. reaction
  136272. hofmann
  136273. reaction
  136274. everett
  136275. wallis
  136276. organi
  136277. homoaldol
  136278. reaction
  136279. overcome
  136280. problems
  136281. regio
  136282. hunsdiecker
  136283. related
  136284. reactions
  136285. hydrides
  136286. aluminum
  136287. gallium
  136288. indium
  136289. thallium
  136290. reeva
  136291. hydrogenolysis
  136292. organic
  136293. halides
  136294. hypoiodite
  136295. reaction
  136296. introduction
  136297. intramolecular
  136298. dole-23-quinodimetha
  136299. strategy
  136300. synthesis
  136301. dole-23-quinodimetha
  136302. strategy
  136303. synthesis
  136304. importance
  136305. intramolecular
  136306. solvation
  136307. organomagnesiu
  136308. importance
  136309. polarity
  136310. steric
  136311. effects
  136312. determining
  136313. importance
  136314. polarity
  136315. strength
  136316. steric
  136317. factors
  136318. inclusion
  136319. pyrrolizidine
  136320. alkaloids
  136321. cyclodextrins
  136322. initiation
  136323. cyclisation
  136324. using
  136325. 3-methylcyclohe
  136326. 2-enone
  136327. inositol
  136328. phosphates
  136329. chemical
  136330. synthesis
  136331. biological
  136332. insertion
  136333. alkynes
  136334. metal-metal
  136335. bonds
  136336. organic-
  136337. insertion
  136338. olefins
  136339. metal-carbon
  136340. bonds
  136341. interaction
  136342. silicon
  136343. positively
  136344. charged
  136345. carbon
  136346. interaction
  136347. thiolo
  136348. selenolesters
  136349. phosphorus
  136350. intramolecular
  136351. aromatic
  136352. friedel-crafts
  136353. reaction
  136354. intramolecular
  136355. diels-ald
  136356. reaction
  136357. intramolecular
  136358. diels-alder
  136359. reaction
  136360. intramolecular
  136361. diels-alder
  136362. reaction
  136363. 14-membered
  136364. intramolecular
  136365. trapping
  136366. reaction
  136367. useful
  136368. intramolecular
  136369. trapping
  136370. reaction
  136371. useful
  136372. intramolecular
  136373. mannich
  136374. related
  136375. reactions
  136376. intramolecular
  136377. silyl
  136378. modified
  136379. sakurai
  136380. reaction
  136381. intramolecular
  136382. reaction
  136383. introduction
  136384. functional
  136385. groups
  136386. unsaturated
  136387. syste
  136388. introduction
  136389. nitrile
  136390. groups
  136391. heterocycles
  136392. ionic
  136393. reduction
  136394. vinyl
  136395. stannanes
  136396. ireland-claisen
  136397. rearrangement
  136398. isocyani
  136399. e-cyanide
  136400. rearrangement
  136401. mechanism
  136402. preparati
  136403. isoinversion
  136404. principle
  136405. general
  136406. model
  136407. chemical
  136408. selec
  136409. isomerisation
  136410. olefins
  136411. base-catalysed
  136412. isomerisa
  136413. isoxazoline
  136414. route
  136415. molecules
  136416. nature
  136417. jacobsen
  136418. reaction
  136419. jacobsen
  136420. reaction
  136421. irvin
  136422. smith
  136423. organic
  136424. reactions
  136425. klingemann
  136426. reaction
  136427. robert
  136428. phillips
  136429. organic
  136430. react
  136431. kinetic
  136432. range
  136433. carbene
  136434. pyridine
  136435. ylide
  136436. forming
  136437. reaction
  136438. kinetics
  136439. thermodynamics
  136440. radical
  136441. reactions
  136442. kinetics
  136443. ylide
  136444. forming
  136445. reaction
  136446. between
  136447. triplet
  136448. diphe
  136449. knoevenagel
  136450. condensation
  136451. knoevenagel
  136452. condensation
  136453. jones
  136454. organic
  136455. reactions
  136456. volum
  136457. knoevenagel
  136458. reaction
  136459. lanthanide
  136460. induced
  136461. shift
  136462. technique
  136463. applications
  136464. confo
  136465. lateral
  136466. metalation
  136467. isoxazoles
  136468. lateral
  136469. metalation
  136470. isoxazoles
  136471. review
  136472. least
  136473. motion
  136474. principle
  136475. concertedness
  136476. mechanisms
  136477. leimgruber
  136478. batcho
  136479. indole
  136480. synthesis
  136481. leimgruber
  136482. batcho
  136483. indole
  136484. synthesis
  136485. using
  136486. nitro
  136487. aromatics
  136488. familiar
  136489. reactions
  136490. organocadmium
  136491. reagents
  136492. leuckart
  136493. reaction
  136494. leuckart
  136495. reaction
  136496. maurice
  136497. moore
  136498. organic
  136499. reactions
  136500. lithium
  136501. reexamined
  136502. logic
  136503. chemical
  136504. synthesis
  136505. logic
  136506. chemical
  136507. synthesis
  136508. multistep
  136509. synthesis
  136510. compl
  136511. mannich
  136512. reaction
  136513. mannich
  136514. reaction
  136515. blicke
  136516. organic
  136517. reactions
  136518. volume
  136519. mechanism
  136520. epoxidation
  136521. olefins
  136522. mechanism
  136523. organocuprate
  136524. 14-addition
  136525. reactions
  136526. mechanism
  136527. allylperoxyl
  136528. rearrangement
  136529. radical
  136530. mechanism
  136531. dehydration
  136532. alcohols
  136533. hydration
  136534. mechanism
  136535. lithium
  136536. halogen
  136537. interchange
  136538. reaction
  136539. mechanism
  136540. mitsunobu
  136541. azide
  136542. modification
  136543. mechanisms
  136544. nucleophilic
  136545. substitution
  136546. aliphati
  136547. photocycloaddition
  136548. arenes
  136549. alkenes
  136550. metal-ammonia
  136551. reduction
  136552. aromatic
  136553. compounds
  136554. metallation
  136555. reaction
  136556. organolithium
  136557. compounds
  136558. michael
  136559. reaction
  136560. microbiological
  136561. transformation
  136562. diterpenoids
  136563. mitsunobu
  136564. reaction
  136565. molecular
  136566. basis
  136567. biological
  136568. order
  136569. amide-amide
  136570. molecular
  136571. orbital
  136572. modeling
  136573. radical
  136574. diels-ald
  136575. molecules
  136576. r2c-x-cr2
  136577. including
  136578. azomethine
  136579. carbonyl
  136580. n-carboxylic
  136581. acids
  136582. nitrogen
  136583. heterocycles
  136584. nature
  136585. radicals
  136586. involved
  136587. grignard
  136588. reagent
  136589. formatio
  136590. nazarov
  136591. cyclisation
  136592. nazarov
  136593. cyclization
  136594. reaction
  136595. nitration
  136596. phenyl-substituted
  136597. heterocycles
  136598. nitrile
  136599. oxide
  136600. isoxazoline
  136601. route
  136602. higher
  136603. carbon
  136604. dialdos
  136605. nitrosation
  136606. aliphatic
  136607. carbon
  136608. atoms
  136609. nitrosation
  136610. aliphatic
  136611. carbon
  136612. atoms
  136613. oscar
  136614. touster
  136615. oppenaner
  136616. oxidation
  136617. djerassi
  136618. organic
  136619. reactions
  136620. oppenauer
  136621. oxidation
  136622. organic
  136623. chemistry
  136624. synthesis
  136625. organic
  136626. chemistry
  136627. marine
  136628. products
  136629. organic
  136630. chemistry
  136631. polycoordinated
  136632. iodine
  136633. organic
  136634. chemistry
  136635. superoxide
  136636. organometallic
  136637. chemistry
  136638. group
  136639. elements
  136640. organometallic
  136641. chemistry
  136642. transition
  136643. metals
  136644. organosulfur
  136645. chemistry
  136646. genus
  136647. allium
  136648. implications
  136649. orgin
  136650. greater
  136651. 200:1
  136652. enantioselectivity
  136653. overlap
  136654. component
  136655. stereoelectronic
  136656. factor
  136657. remote
  136658. oxenoid
  136659. character
  136660. metalated
  136661. hydroperoxides
  136662. oxidation
  136663. oxazolines
  136664. oxazoles
  136665. oxidation
  136666. organic
  136667. nitrogen
  136668. compounds
  136669. tetraa
  136670. oxygenation
  136671. vinylcyclopropanes
  136672. entry
  136673. stereD
  136674. palladium
  136675. catalyzed
  136676. asymmetric
  136677. a-allylation
  136678. carbonyl
  136679. palladium
  136680. catalyzed
  136681. cross
  136682. coupling
  136683. reactions
  136684. organoti
  136685. palladium-catalysed
  136686. cross-coupling
  136687. reactions
  136688. organoti
  136689. palladium-catalyzed
  136690. hydroarylation
  136691. drovinylation
  136692. partial
  136693. catalytic
  136694. oxidation
  136695. methane
  136696. oxygen-co
  136697. passerini
  136698. reactions
  136699. paterno-buchi
  136700. reaction
  136701. pauson-khand
  136702. cycloaddition
  136703. reaction
  136704. synthesis
  136705. pauson-khand
  136706. reactions
  136707. pechmann
  136708. reaction
  136709. pecific
  136710. synthesis
  136711. pyridines
  136712. oligopyridines
  136713. perkin
  136714. reaction
  136715. perkin
  136716. reaction
  136717. related
  136718. reactions
  136719. perkin
  136720. reaction
  136721. related
  136722. reactions
  136723. johnson
  136724. persulfate
  136725. oxidation
  136726. phenols
  136727. arylamines
  136728. peterson
  136729. olefination
  136730. reaction
  136731. peterson
  136732. reaction
  136733. phenylenes
  136734. photo-oxygenation
  136735. olefins
  136736. zwitterioni
  136737. photochemical-synthe
  136738. chemicals
  136739. sunlight
  136740. photochemistry
  136741. spectroscopy
  136742. gamma
  136743. unsaturate
  136744. photochemistry
  136745. acetylenic
  136746. ethers
  136747. novel
  136748. carbon
  136749. oxyge
  136750. photochemistry
  136751. azines
  136752. photochemistry
  136753. carbenium
  136754. related
  136755. species
  136756. photochemistry
  136757. coumarins
  136758. photochemistry
  136759. enamides
  136760. photochemistry
  136761. imines
  136762. photochemistry
  136763. iminium
  136764. salts
  136765. related
  136766. heteroaromat
  136767. photochemistry
  136768. polyhalocompounds
  136769. dehalogenation
  136770. photochemistry
  136771. thiocar
  136772. compounds
  136773. photoexited
  136774. states
  136775. organic
  136776. anions
  136777. photoreactivity
  136778. thiocarbonyl
  136779. compounds
  136780. pictet
  136781. spengler
  136782. reaction
  136783. biogenic
  136784. tryptamines
  136785. format
  136786. pictet
  136787. spengler
  136788. synthesis
  136789. tetrahydroisoquinoli
  136790. pictet-spengler
  136791. condensation
  136792. direction
  136793. pinacol
  136794. rearrangement
  136795. polonovski
  136796. reaction
  136797. polyketide
  136798. metabolites
  136799. porphyrins
  136800. annulene
  136801. chemist's
  136802. perspective
  136803. paration
  136804. ketones
  136805. reaction
  136806. organolithiu
  136807. preparartion
  136808. methylated
  136809. pyridinium
  136810. salts
  136811. preparation
  136812. chemical
  136813. properties
  136814. thioamides
  136815. preparation
  136816. reactions
  136817. diazomethane
  136818. preparation
  136819. dihydroisoquinolines
  136820. related
  136821. compo
  136822. preparation
  136823. 34-dihydroisoquinoli
  136824. related
  136825. compound
  136826. preparation
  136827. aliphatic
  136828. fluorine
  136829. compounds
  136830. preparation
  136831. aliphatic
  136832. fluorine
  136833. compounds
  136834. albert
  136835. preparation
  136836. amines
  136837. reductive
  136838. alkylation
  136839. preparation
  136840. amines
  136841. reductive
  136842. alkylation
  136843. william
  136844. preparation
  136845. aromatic
  136846. arsonic
  136847. arsinic
  136848. acids
  136849. preparation
  136850. glucals
  136851. palladium
  136852. catalyzed
  136853. preparation
  136854. grignard
  136855. reagents
  136856. hydromagnesiati
  136857. preparation
  136858. acylpyrazoles
  136859. their
  136860. behavior
  136861. toward
  136862. preparation
  136863. olefins
  136864. pyrolysis
  136865. xanthates
  136866. preparation
  136867. pyrrole
  136868. carboxylates
  136869. vinyl
  136870. sulfone
  136871. preparation
  136872. thiazoles
  136873. preparation
  136874. thiazoles
  136875. richard
  136876. wiley
  136877. england
  136878. preparation
  136879. thiophenes
  136880. tetrahydrothiophenes
  136881. preparation
  136882. unsymmetrical
  136883. biaryls
  136884. diazo
  136885. reacti
  136886. preparative
  136887. chemistry
  136888. n-functional
  136889. orthocarboni
  136890. prepuration
  136891. thiophenes
  136892. tetrahydrothiophenes
  136893. donal
  136894. present
  136895. state
  136896. chemistry
  136897. aminonitrenes
  136898. pressure
  136899. effect
  136900. pericyclic
  136901. rearrangements
  136902. principle
  136903. least
  136904. nuclear
  136905. motion
  136906. stereoelectronic
  136907. principle
  136908. least
  136909. nuclear
  136910. motion
  136911. theory
  136912. prins
  136913. carbonyl
  136914. reactions
  136915. prins
  136916. reaction
  136917. properties
  136918. organic
  136919. liquids
  136920. relevant
  136921. their
  136922. pschorr
  136923. synthesis
  136924. related
  136925. diazonium
  136926. closure
  136927. pummerer
  136928. cyclization
  136929. route
  136930. ibophyllidine
  136931. alkaloid
  136932. pummerer
  136933. reaction
  136934. sulfinyl
  136935. compounds
  136936. pursuit
  136937. selectivity
  136938. radical
  136939. reactions
  136940. pyridoacridine
  136941. alkaloids
  136942. pyrolytic
  136943. rearrangement
  136944. alkynoyl
  136945. methylpyrazoles
  136946. quantitative
  136947. description
  136948. amino
  136949. peptide
  136950. prote
  136951. quinolizinium
  136952. analogs
  136953. radical
  136954. cyclization
  136955. approach
  136956. morphine
  136957. models
  136958. ramberg-backlund
  136959. rearrangement
  136960. range
  136961. radical
  136962. processes
  136963. nitration
  136964. nitric
  136965. rapid
  136966. steps
  136967. nucleophilic
  136968. vinylic
  136969. addition-elimination
  136970. reaction
  136971. active
  136972. methylene
  136973. reagents
  136974. sulfur
  136975. reaction
  136976. carbon
  136977. radicals
  136978. sulfur
  136979. convenient
  136980. reaction
  136981. diazoacetic
  136982. esters
  136983. alkenes
  136984. alkynes
  136985. reaction
  136986. diazomethane
  136987. derivatives
  136988. aldehy
  136989. reaction
  136990. ethyl
  136991. diazoacetate
  136992. styrene
  136993. oxide
  136994. reaction
  136995. halogens
  136996. silver
  136997. salts
  136998. carboxylic
  136999. reaction
  137000. isatin
  137001. azomethine
  137002. ylides
  137003. oxoindolin
  137004. reaction
  137005. nitriles
  137006. chlorides
  137007. presence
  137008. reaction
  137009. sodium
  137010. hydrogen
  137011. telluride
  137012. unsaturat
  137013. reactions
  137014. dianions
  137015. carboxylic
  137016. acids
  137017. ester
  137018. reactions
  137019. diazoacetic
  137020. esters
  137021. alkenes
  137022. alkynes
  137023. reactions
  137024. dinitrogen
  137025. transition
  137026. metal
  137027. complex
  137028. reactivity
  137029. acridinium
  137030. salts
  137031. related
  137032. compounds
  137033. reactivity
  137034. cyclic
  137035. acetals
  137036. aldoses
  137037. aldosides
  137038. reactivity
  137039. phosphorus-containin
  137040. sulfenyl
  137041. chlorides
  137042. reactivity-selectivi
  137043. principle
  137044. fiction
  137045. reduction
  137046. organic
  137047. compounds
  137048. salts
  137049. reformatsky
  137050. reaction
  137051. reformatsky
  137052. reaction
  137053. reformatsky
  137054. reaction
  137055. michael
  137056. rathke
  137057. organic
  137058. reactions
  137059. reformatsky
  137060. reaction
  137061. ralph
  137062. shriner
  137063. organic
  137064. reactions
  137065. regioselective
  137066. hydroformylation
  137067. vinylsilanes
  137068. remark
  137069. reimer-tiemann
  137070. reaction
  137071. relationship
  137072. between
  137073. order
  137074. lengt
  137075. relevance
  137076. chirality
  137077. study
  137078. biological
  137079. activi
  137080. resolution
  137081. alcohols
  137082. resolution
  137083. alcohols
  137084. ingersoll
  137085. organic
  137086. reactions
  137087. ritter
  137088. reaction
  137089. ritter
  137090. reaction
  137091. krimen
  137092. donald
  137093. organic
  137094. robinson
  137095. annelation
  137096. related
  137097. reactions
  137098. aromatic
  137099. interactions
  137100. molecular
  137101. recognition
  137102. carbenes
  137103. chemistry
  137104. coordinated
  137105. carbenes
  137106. chemistry
  137107. low-coordinated
  137108. high-pressure
  137109. methods
  137110. organic
  137111. chemistry
  137112. interactions
  137113. chemistry
  137114. reformatsky
  137115. reaction
  137116. metal
  137117. centers
  137118. reduction
  137119. carboxylation
  137120. aminosugar
  137121. helix
  137122. binding
  137123. thiol-in@
  137124. dimethyl
  137125. sulphoxide@
  137126. stille
  137127. coupling
  137128. reaction
  137129. triflates
  137130. allene
  137131. synthesis
  137132. novel
  137133. reactivity
  137134. heterodinucle@
  137135. synthesis
  137136. 6h-pyrido
  137137. carbazoles@
  137138. synthesis
  137139. insect
  137140. pheromones
  137141. synthesis
  137142. polysaccharides
  137143. 1986@
  137144. ermal
  137145. addition
  137146. carbon-carbon
  137147. multiple
  137148. bonds
  137149. stra@
  137150. total
  137151. synthesis
  137152. racemic
  137153. gelsimine@
  137154. chiral
  137155. organoboranes
  137156. organic
  137157. synthesis@
  137158. zeolit
  137159. organic
  137160. reactions@
  137161. wittig
  137162. olefination
  137163. reaction
  137164. carbonyl
  137165. compounds
  137166. othe@
  137167. their
  137168. theis@
  137169. theodore@
  137170. theory
  137171. thermal
  137172. light
  137173. induced
  137174. electron
  137175. transfer
  137176. reactions
  137177. thermal
  137178. rearrangements
  137179. alkynes
  137180. under
  137181. flash
  137182. vacuum
  137183. pyrolys@
  137184. thermolysis
  137185. metal
  137186. centers
  137187. reduction
  137188. carboxylation
  137189. metals
  137190. carbene
  137191. synthon
  137192. introduction
  137193. secondary
  137194. orbital
  137195. interactions
  137196. controlling
  137197. silver
  137198. salts
  137199. organic
  137200. processes
  137201. solid-phase
  137202. fragment
  137203. condensation
  137204. peptid
  137205. sulfur
  137206. functionalities
  137207. activating
  137208. directi
  137209. sulphur
  137210. functionality
  137211. activating
  137212. directin
  137213. alpha-effect
  137214. thermolysis
  137215. photolysis
  137216. tmscl
  137217. gilman
  137218. cuprate
  137219. 14-addtion
  137220. reactions
  137221. carbenoids
  137222. organic
  137223. synthesis
  137224. roles
  137225. silver
  137226. salts
  137227. organic
  137228. processes
  137229. rosenmund
  137230. reduction
  137231. chlorides
  137232. aldehydes
  137233. rosenmund
  137234. reduction
  137235. chlorides
  137236. aldehydes
  137237. erich
  137238. meyer-schuster
  137239. rearrangements
  137240. schlosser
  137241. butyllithium
  137242. butoxide
  137243. mixtures
  137244. schmidt
  137245. reaction
  137246. schmidt
  137247. reaction
  137248. wolff
  137249. organic
  137250. reactions
  137251. volume
  137252. schmidt
  137253. reaction
  137254. dialkyl
  137255. acylphosphonates
  137256. scope
  137257. mechanism
  137258. cyclopropyliminium
  137259. rearra
  137260. selective
  137261. functionalization
  137262. saturated
  137263. hydrocarbons
  137264. semipinacol
  137265. other
  137266. rearrangements
  137267. sesterterpenoids
  137268. significance
  137269. molecular
  137270. shape
  137271. complementarity
  137272. significance
  137273. lengths
  137274. orders
  137275. silicon-heteroatom
  137276. simple
  137277. preparation
  137278. aldehydes
  137279. ketones
  137280. photo
  137281. single
  137282. electron
  137283. shift
  137284. fundamental
  137285. process
  137286. organi
  137287. skraup
  137288. synthesis
  137289. quinolines
  137290. skraup
  137291. synthesis
  137292. quinolines
  137293. manske
  137294. marshall
  137295. smiles
  137296. related
  137297. rearrangements
  137298. aromatic
  137299. systems
  137300. smiles
  137301. related
  137302. rearrangements
  137303. aromatic
  137304. systems
  137305. smiles
  137306. rearrangement
  137307. polyfluoroaromatic
  137308. series
  137309. anrorc
  137310. mechanism
  137311. mechanism
  137312. nucleophilic
  137313. dimethyl
  137314. sulphoxide
  137315. sommelet
  137316. reaction
  137317. stabilization
  137318. reactivity
  137319. strained
  137320. cyclic
  137321. alkynes
  137322. stereochemistry
  137323. cyclobutane
  137324. heterocyclic
  137325. analogs
  137326. stereochemistry
  137327. cyclohexyl
  137328. vinylic
  137329. radicals
  137330. stereochemistry
  137331. electrophilic
  137332. additions
  137333. olefins
  137334. stereochemistry
  137335. germanium
  137336. compounds
  137337. stereochemistry
  137338. nucleophilic
  137339. substitution
  137340. tetracoo
  137341. stereochemistry
  137342. organometallic
  137343. compounds
  137344. rhodium
  137345. stereochemistry
  137346. organometallic
  137347. compounds
  137348. prepa
  137349. stereochemistry
  137350. organosilicon
  137351. compounds
  137352. stereochemistry
  137353. rearrangements
  137354. hetaryl
  137355. stereoselective
  137356. functionalisation
  137357. tributylstan
  137358. stereoselectivity
  137359. intramolecular
  137360. radical
  137361. reactio
  137362. steric
  137363. factor
  137364. medicinal
  137365. chemistry
  137366. dissymmetric
  137367. probes
  137368. stevens
  137369. related
  137370. rearrangements
  137371. stille
  137372. coupling
  137373. reaction
  137374. triflates
  137375. allene
  137376. stille
  137377. coupling
  137378. reaction
  137379. triflates
  137380. tribut
  137381. stobbe
  137382. condensation
  137383. stobbe
  137384. condensation
  137385. william
  137386. johnson
  137387. guido
  137388. structure
  137389. mechanism
  137390. formation
  137391. ozonides
  137392. structure
  137393. properties
  137394. complexes
  137395. simulating
  137396. molecul
  137397. structure
  137398. equimolar
  137399. complexes
  137400. halides
  137401. structure
  137402. lithium
  137403. coumpounds
  137404. sulfones
  137405. sulfoximides
  137406. structure
  137407. lithium
  137408. cuprates
  137409. lower
  137410. order
  137411. structure
  137412. lithium
  137413. compounds
  137414. sulfones
  137415. structure-directed
  137416. synthesis
  137417. cyclacene
  137418. polyacene
  137419. surface
  137420. nature
  137421. grignard
  137422. reagent
  137423. formation
  137424. steric
  137425. course
  137426. bimolecular
  137427. olefin-forming
  137428. utility
  137429. alpha-amino
  137430. alkoxides
  137431. synthesis
  137432. induced
  137433. cycloaromatization
  137434. diene
  137435. synthesis
  137436. glycosidation
  137437. n-acetylneuraminic
  137438. synthesis
  137439. novel
  137440. reactivity
  137441. heterodinucle
  137442. synthesis
  137443. properties
  137444. covalent
  137445. organic
  137446. perchlorate
  137447. synthesis
  137448. properties
  137449. 23-epoxypropyl
  137450. carbazoles
  137451. synthesis
  137452. properties
  137453. organized
  137454. polyaza
  137455. cavity-sha
  137456. synthesis
  137457. properties
  137458. thioaldehydes
  137459. synthesis
  137460. properties
  137461. unsaturated
  137462. nitro
  137463. compounds
  137464. synthesis
  137465. reactions
  137466. prismanes
  137467. recent
  137468. developments
  137469. synthesis
  137470. stereochemistry
  137471. chiral
  137472. organic
  137473. molecule
  137474. synthesis
  137475. transformations
  137476. uronic
  137477. nucleosides
  137478. synthesis
  137479. thienopyrroles
  137480. synthesis
  137481. 2-aminobenzophenones
  137482. synthesis
  137483. phanes
  137484. synthesis
  137485. functionalized
  137486. chloro
  137487. methyl
  137488. synthesis
  137489. 3-substituted
  137490. pyrroles
  137491. pyrrole
  137492. synthesis
  137493. hydroxyindoles
  137494. nenitzescu
  137495. reaction
  137496. synthesis
  137497. 5-hydroxyindoles
  137498. nenitzescu
  137499. reaction
  137500. synthesis
  137501. 6h-pyrido
  137502. carbazoles
  137503. synthesis
  137504. acetylenes
  137505. thomas
  137506. jacobs
  137507. organic
  137508. reaction
  137509. synthesis
  137510. aldehydes
  137511. carboxylic
  137512. acids
  137513. synthesis
  137514. aliphatic
  137515. alicyclic
  137516. nitro
  137517. compounds
  137518. synthesis
  137519. alpha-methylene
  137520. lactones
  137521. synthesis
  137522. benzoins
  137523. synthesis
  137524. benzoins
  137525. walter
  137526. johannes
  137527. synthesis
  137528. brassinosteroid
  137529. synthesis
  137530. carbocyclic
  137531. eight-membered
  137532. rings
  137533. synthesis
  137534. carbohydrate
  137535. derivatives
  137536. acyclic
  137537. precu
  137538. synthesis
  137539. cyclic
  137540. ethers
  137541. molybdenum
  137542. alkyliden
  137543. synthesis
  137544. drimane
  137545. sesquiterpenoids
  137546. synthesis
  137547. episulphones
  137548. olefins
  137549. sulphenes
  137550. synthesis
  137551. fomannosin
  137552. illudol
  137553. synthesis
  137554. heterocycles
  137555. indolin
  137556. derivatives
  137557. synthesis
  137558. heterocyclic
  137559. compounds
  137560. starting
  137561. lacton
  137562. synthesis
  137563. insect
  137564. juvenile
  137565. hormones
  137566. their
  137567. analogue
  137568. synthesis
  137569. insect
  137570. pheromones
  137571. synthesis
  137572. insect
  137573. pheromones
  137574. synthesis
  137575. isoquinolines
  137576. pomeranz
  137577. fritsch
  137578. react
  137579. synthesis
  137580. isoquinolines
  137581. pomeranz-fritsch
  137582. react
  137583. synthesis
  137584. ketones
  137585. halides
  137586. organometalli
  137587. synthesis
  137588. ketones
  137589. hdides
  137590. organometallic
  137591. synthesis
  137592. lactams
  137593. synthesis
  137594. macrocyclic
  137595. lactones
  137596. approaches
  137597. complex
  137598. synthesis
  137599. mevinic
  137600. acids
  137601. synthesis
  137602. modified
  137603. oligonucleotides
  137604. phosphoram
  137605. synthesis
  137606. natural
  137607. heterocyclic
  137608. products
  137609. hetero
  137610. synthesis
  137611. natural
  137612. lactam
  137613. antibiotics
  137614. synthesis
  137615. nucleotides
  137616. synthesis
  137617. optically
  137618. active
  137619. phenylthio
  137620. aldehydes
  137621. synthesis
  137622. organochlorine
  137623. compounds
  137624. one-carbon
  137625. synthesis
  137626. phosphonic
  137627. phosphinic
  137628. acids
  137629. synthesis
  137630. phosphonic
  137631. phosphinic
  137632. acids
  137633. gennady
  137634. synthesis
  137635. polyquinanes
  137636. polyquinenes
  137637. weiss
  137638. synthesis
  137639. polysaccharides
  137640. synthesis
  137641. prostaglandin
  137642. synthesis
  137643. pyridines
  137644. quinolines
  137645. other
  137646. related
  137647. synthesis
  137648. radiolabeled
  137649. compounds
  137650. organometallic
  137651. synthesis
  137652. specific
  137653. ribonucleotides
  137654. unrelated
  137655. synthesis
  137656. stable
  137657. isolable
  137658. planar-tetracoordina
  137659. carbon
  137660. synthesis
  137661. substituted
  137662. ferrocenes
  137663. other
  137664. cyclope
  137665. synthesis
  137666. substituted
  137667. pyrrolidines
  137668. samarium
  137669. synthesis
  137670. unusual
  137671. organic
  137672. molecules
  137673. alkanes
  137674. synthesis
  137675. unusual
  137676. organic
  137677. molecules
  137678. azoalkanes
  137679. synthetic
  137680. methodology
  137681. nonracemic
  137682. glycidol
  137683. related
  137684. synthetic
  137685. potentialities
  137686. nitriles
  137687. heterocyclic
  137688. synthetic
  137689. utility
  137690. 2-oxazolines
  137691. synthetic
  137692. utility
  137693. alpha
  137694. amino
  137695. alkoxides
  137696. synthetic
  137697. utility
  137698. oxazolines
  137699. aromatic
  137700. substitution
  137701. synthetic
  137702. utility
  137703. oxyallyl
  137704. cations
  137705. ermal
  137706. addition
  137707. carbon-carbon
  137708. multiple
  137709. bonds
  137710. taxane
  137711. alkaloids
  137712. termination
  137713. palladium
  137714. catalysed
  137715. insertion
  137716. reacti
  137717. thermal
  137718. aliphatic
  137719. claisen
  137720. rearrangement
  137721. thermal
  137722. cyclisation
  137723. unsaturated
  137724. carbonyl
  137725. compounds
  137726. thermal
  137727. gas-phase
  137728. synthesis
  137729. heterocycli
  137730. compounds
  137731. thermal
  137732. rearrangement
  137733. dimethylbicyclo
  137734. 3.2.0
  137735. thiele-winter
  137736. acetoxylation
  137737. quinones
  137738. third
  137739. allotropic
  137740. carbon
  137741. torsion
  137742. angle
  137743. concept
  137744. conformational
  137745. analysis
  137746. total
  137747. synthesis
  137748. amphoteronolide
  137749. amphotericin
  137750. total
  137751. synthesis
  137752. epibatidine
  137753. total
  137754. synthesis
  137755. gibberellic
  137756. total
  137757. synthesis
  137758. ionophores
  137759. total
  137760. synthesis
  137761. macrocyclic
  137762. lactones
  137763. total
  137764. synthesis
  137765. natural
  137766. products
  137767. chiron
  137768. approach
  137769. total
  137770. synthesis
  137771. naturally
  137772. occurring
  137773. quinones
  137774. total
  137775. synthesis
  137776. neolemnane
  137777. 14-deoxyisoamijiol
  137778. total
  137779. synthesis
  137780. racemic
  137781. gelsimine
  137782. total
  137783. synthesis
  137784. retigeranic
  137785. total
  137786. synthesis
  137787. saxitoxin
  137788. total
  137789. synthesis
  137790. scopadulcic
  137791. acids
  137792. scopadu
  137793. total
  137794. synthesis
  137795. spiroketal-containin
  137796. natural
  137797. products
  137798. total
  137799. synthesis
  137800. tricyclic
  137801. tetracyclic
  137802. diterpenes
  137803. transformation
  137804. aromatics
  137805. regio-and
  137806. stereocontrol
  137807. transformations
  137808. alkenes
  137809. lactones
  137810. using
  137811. iodoester
  137812. tropane
  137813. alkaloids
  137814. tropane
  137815. alkaloids
  137816. alkaloids
  137817. ullmann
  137818. synthesis
  137819. biaryls
  137820. unambiguous
  137821. specification
  137822. steric
  137823. course
  137824. asymme
  137825. uncatalyzed
  137826. alcoholysis
  137827. furyl
  137828. oxirane
  137829. mechanistic
  137830. unusual
  137831. unexpected
  137832. photoc
  137833. unusual
  137834. stevens
  137835. rearrangements
  137836. dialkylsulfi
  137837. trimethylsilyl
  137838. unsaturated
  137839. ketones
  137840. arene
  137841. cis-diols
  137842. synthesis
  137843. chiral
  137844. organoboranes
  137845. organic
  137846. synthesis
  137847. cyclohexa-35-diene-1
  137848. enantiospecific
  137849. synthesis
  137850. diethylazodicarboxyl
  137851. triphenylphosphine
  137852. enzymes
  137853. catalysis
  137854. reactions
  137855. insoluble
  137856. polymer
  137857. supports
  137858. general
  137859. organic
  137860. isocyanides
  137861. heterocyclic
  137862. synthesis
  137863. isocyanides
  137864. heterocyclic
  137865. synthesis
  137866. review
  137867. butoxycarbonyl
  137868. hydroxylamine
  137869. samarium
  137870. diiodide
  137871. organic
  137872. lymer
  137873. synthesi
  137874. selenium-containing
  137875. intermediates
  137876. mediate
  137877. shape
  137878. selective
  137879. stationary
  137880. phases
  137881. bifunctional
  137882. reagents
  137883. organic
  137884. synthesis
  137885. bifunctional
  137886. reagents
  137887. organic
  137888. synthesis
  137889. thiocarbonyl
  137890. compounds
  137891. carbon-carbon
  137892. compounds
  137893. carbohydrate
  137894. nucleoside
  137895. zeolit
  137896. organic
  137897. reactions
  137898. utilisation
  137899. sulfoximines
  137900. derivatives
  137901. reagents
  137902. utility
  137903. nitroacetic
  137904. esters
  137905. organic
  137906. utility
  137907. pummerer
  137908. rearrangement
  137909. intermediates
  137910. variety
  137911. thermal
  137912. pericyclic
  137913. reactions
  137914. versatile
  137915. chemistry
  137916. thiophenes
  137917. effects
  137918. vilsmeier
  137919. reaction
  137920. dithioketals
  137921. facile
  137922. method
  137923. vilsmeier-haack
  137924. reaction
  137925. vinylcyclopropane-cy
  137926. rearrangement
  137927. virtue
  137928. methylenecyclopropan
  137929. terminators
  137930. intramolec
  137931. braun
  137932. cyanogen
  137933. bromide
  137934. reaction
  137935. braun
  137936. cyanogen
  137937. bromide
  137938. reaction
  137939. howard
  137940. hapman
  137941. lgerodt
  137942. reaction
  137943. willgerodt
  137944. reaction
  137945. willgerodt
  137946. reaction
  137947. marvin
  137948. carmack
  137949. spielman
  137950. wittig
  137951. olefination
  137952. modifications
  137953. involving
  137954. phosphory
  137955. wittig
  137956. olefination
  137957. reaction
  137958. modifications
  137959. involving
  137960. wittig
  137961. olefination
  137962. reaction
  137963. carbonyl
  137964. compounds
  137965. wittig
  137966. reaction
  137967. wittig
  137968. reaction
  137969. review
  137970. wittig
  137971. reaction
  137972. adalbert
  137973. maercker
  137974. organic
  137975. reactions
  137976. wittig
  137977. reaction
  137978. industrial
  137979. practice
  137980. wittig
  137981. reaction
  137982. industrial
  137983. practice
  137984. review
  137985. wittig
  137986. rearrangement
  137987. kishner
  137988. reducbon
  137989. david
  137990. organic
  137991. reactions
  137992. volum
  137993. wolff
  137994. rearrangement
  137995. wolff
  137996. rearrangement
  137997. alpha-diazocarbonyl
  137998. compounds
  137999. wolff
  138000. rearrangement
  138001. diazo
  138002. carbonyl
  138003. compounds
  138004. wolff
  138005. rearrangement
  138006. oxirene
  138007. ketene
  138008. interconversion
  138009. wolff-kishner
  138010. reduction
  138011. erful
  138012. world
  138013. organosilicon
  138014. chemistry
  138015. zinin
  138016. reduction
  138017. nitroarenes
  138018. zinin
  138019. reduction
  138020. nitroarenes
  138021. porter
  138022. organic
  138023. reacti
  138024. theander
  138025. thebtaranonth
  138026. thebtaranonth
  138027. thebtaranonth
  138028. cyclization
  138029. reactions
  138030. thechemistry
  138031. theimer
  138032. their
  138033. their
  138034. their
  138035. theme
  138036. themodern
  138037. theodora
  138038. theodore
  138039. theophil
  138040. theopold
  138041. theoretical
  138042. theoretical
  138043. experimental
  138044. study
  138045. regioselectivity
  138046. theoretical
  138047. investigations
  138048. thermochemistry
  138049. therma
  138050. theoretical
  138051. secondary
  138052. kinetic
  138053. isotope
  138054. effects
  138055. interp
  138056. theoretical
  138057. studies
  138058. effects
  138059. hydration
  138060. organic
  138061. theoretical
  138062. studies
  138063. carbometalation
  138064. cyclopropene
  138065. trans
  138066. theoretical
  138067. study
  138068. wittig
  138069. olefination
  138070. reaction
  138071. theoretically
  138072. theories
  138073. theoryR
  138074. theory
  138075. theory
  138076. mechanism
  138077. allylidenecyclopropa
  138078. methylen
  138079. theory
  138080. gas-phase
  138081. solution
  138082. stereoselectivites
  138083. hydri
  138084. therapeutic
  138085. therapeutically
  138086. therapy
  138087. there
  138088. therese
  138089. thermal
  138090. thermal
  138091. sigmatropic
  138092. rearrangements
  138093. thermal
  138094. catalyzed
  138095. diels
  138096. alder
  138097. reactions
  138098. chiral
  138099. thermal
  138100. light
  138101. induced
  138102. electron
  138103. transfer
  138104. reactions
  138105. thermal
  138106. photochemical
  138107. addition
  138108. dienophiles
  138109. arenes
  138110. thermal
  138111. photochemical
  138112. reaction
  138113. acetylindole
  138114. thermal
  138115. photochemical
  138116. transformations
  138117. hetero
  138118. thermal
  138119. cyclization
  138120. dienes
  138121. enynes
  138122. enones
  138123. related
  138124. unsat
  138125. thermal
  138126. cycloaddition
  138127. reactions
  138128. thiocarbonyl
  138129. compounds
  138130. thermal
  138131. cycloadditions
  138132. thermal
  138133. cyclobutane
  138134. formation
  138135. thermal
  138136. decomposition
  138137. aliphatic
  138138. nitro
  138139. compounds
  138140. thermal
  138141. decomposition
  138142. thiirane
  138143. methylthiirane
  138144. thermal
  138145. electrocyclic
  138146. reactions
  138147. thermal
  138148. electrocyclic
  138149. spirocyclization
  138150. benzoquinoneimin
  138151. thermal
  138152. photochemical
  138153. transition
  138154. metal
  138155. mediated
  138156. routes
  138157. thermal
  138158. reaction
  138159. cyclopropanone
  138160. ketals
  138161. scope
  138162. applicat
  138163. thermal
  138164. reactions
  138165. thiyl
  138166. radicals
  138167. thermal
  138168. rearrangements
  138169. propargyl
  138170. rearrangement
  138171. thermal
  138172. rearrangements
  138173. alkynes
  138174. under
  138175. flash
  138176. vacuum
  138177. pyrolys
  138178. thermal
  138179. rearrangements
  138180. aromatic
  138181. compounds
  138182. thermal
  138183. rearrangements
  138184. fluorine-containing
  138185. cyclopropanes
  138186. thermal
  138187. ring-opening
  138188. cyclopropyl
  138189. derivatives
  138190. activat
  138191. thermally
  138192. thermochemical
  138193. thermochemistry
  138194. thermochromic
  138195. thermochromic
  138196. distibines
  138197. dibismuthines
  138198. thermochromism
  138199. thermodynamic
  138200. thermodynamic
  138201. kinetic
  138202. macrocycle
  138203. interaction
  138204. thermodynamic
  138205. kinetic
  138206. macrocycle
  138207. interactions
  138208. thermodynamic
  138209. properties
  138210. isomerization
  138211. reactions
  138212. thermodynamical
  138213. thermodynamical
  138214. geometrical
  138215. characterization
  138216. molecula
  138217. thermodynamically
  138218. thermodynamics
  138219. thermolabile
  138220. thermolysis
  138221. thermolysis
  138222. thermolysis
  138223. photolysis
  138224. sugar
  138225. diazides
  138226. thermolysis
  138227. phenylmethyl
  138228. dioxetane
  138229. radical
  138230. thermolysis
  138231. substituted
  138232. norbornadienes
  138233. thermolysis
  138234. azidomethyl
  138235. ketone
  138236. methyl
  138237. phenylsufo
  138238. thermolysis
  138239. diazotetraphenylcycl
  138240. presence
  138241. amine
  138242. thermolysis
  138243. oxadiazoline
  138244. solution
  138245. remarkable
  138246. cascade
  138247. thermolytic
  138248. thermotropic
  138249. thermotropic
  138250. liquid
  138251. crystals
  138252. reaction
  138253. media
  138254. mechanist
  138255. thernlochemistry
  138256. these
  138257. theses
  138258. thesis
  138259. thetic
  138260. thetotal
  138261. thexylborane
  138262. thexylborane
  138263. highly
  138264. versatile
  138265. reagent
  138266. organic
  138267. synthesi
  138268. thf/hmpa
  138269. thiaalkenyl
  138270. thiaarenes
  138271. thiacrown
  138272. thiacrown
  138273. compounds
  138274. 12-dicyano-12-dithio
  138275. units
  138276. thiacyclobutenes
  138277. thiadiazines
  138278. thiadiazines
  138279. adjacent
  138280. sulfur
  138281. nitrogen
  138282. atoms
  138283. thiadiazol
  138284. thiadiazole
  138285. thiadiazoles
  138286. thian
  138287. thianes
  138288. thianthrenes
  138289. thiaphenothiazines
  138290. thiaspirane
  138291. thiasteroids
  138292. thiation
  138293. thiatriazoles
  138294. thiazaspirocycloalka
  138295. thiazenes
  138296. thiazines
  138297. thiazino
  138298. thiazol
  138299. thiazole
  138300. thiazoles
  138301. thiazoles
  138302. their
  138303. benzo
  138304. derivatives
  138305. thiazolidine
  138306. thiazolidines
  138307. thiazolidinones
  138308. thiazoline
  138309. thiazolines
  138310. thiazolinone
  138311. thiazolium
  138312. thiazolo
  138313. thiazolobenzimidazol
  138314. thiazolyl
  138315. thibblin
  138316. thibblin
  138317. mechanisms
  138318. solvolytic
  138319. alkene
  138320. forming
  138321. elimina
  138322. thiacrown
  138323. compounds
  138324. 12-dicyano-12-dithio
  138325. units@
  138326. thibblin
  138327. mechanisms
  138328. solvolytic
  138329. alkene
  138330. forming
  138331. elimina
  138332. thio@
  138333. thiocarboxylic
  138334. s-ester
  138335. imides@
  138336. thiol-induced@
  138337. thiolesters@
  138338. thionolactones@
  138339. thiophenes
  138340. their
  138341. benzo
  138342. derivatives
  138343. reactivity@
  138344. thiopyrans@
  138345. thoamide
  138346. thioester
  138347. cyclopentane
  138348. synthesis
  138349. trimethylt@
  138350. threading
  138351. molecular
  138352. strings
  138353. molecular
  138354. rings
  138355. synthesis
  138356. three-dimensional@
  138357. threo
  138358. through-bond@
  138359. tikhonov@
  138360. organic
  138361. synthesis
  138362. effective
  138363. synthesis
  138364. titanium
  138365. titanium
  138366. zirconium
  138367. derivatives
  138368. organic
  138369. synthesis@
  138370. titanocene@
  138371. tmsi@
  138372. o-methylbouvardin
  138373. o-methyl-@
  138374. total
  138375. synthesis
  138376. indolizomycin@
  138377. total
  138378. synthesis
  138379. polycarbocyclic
  138380. sesquiterpenes
  138381. survey
  138382. total
  138383. synthesis
  138384. gilvocarcins@
  138385. toward
  138386. thibblin
  138387. mechanisms
  138388. solvolytic
  138389. alkene
  138390. forming
  138391. elimina
  138392. thiel
  138393. thiele-winter
  138394. thiels
  138395. thiem
  138396. thieme
  138397. thieno
  138398. thienopyridines
  138399. thienopyrroles
  138400. thienopyrrolizines
  138401. thienopyrrolizines
  138402. condensed
  138403. triheterocyclic
  138404. systems
  138405. thiepanes
  138406. thiepin
  138407. thiepins
  138408. thiericke
  138409. thietanes
  138410. thietanes
  138411. thietes
  138412. fused-ring
  138413. derivatives
  138414. thiete
  138415. thietes
  138416. thiinium
  138417. thiirane
  138418. thiiranes
  138419. thiiranes
  138420. thiirenes
  138421. thiiranium
  138422. thiiranium
  138423. reaction
  138424. intermediates
  138425. thiiranoradialenes
  138426. thiirans
  138427. thiirenes
  138428. thiirenium
  138429. thilivhali
  138430. thinK
  138431. thin-layer
  138432. thin-layer
  138433. chromatography
  138434. reagents
  138435. detection
  138436. methods
  138437. things
  138438. thinking
  138439. claisen
  138440. rearrangements
  138441. asymmetric
  138442. synthesis
  138443. 44-di
  138444. thioacetals
  138445. thioacetamides
  138446. thioacetates
  138447. thioacid
  138448. thioacylating
  138449. thioaldehydes
  138450. thioaldehydes
  138451. thioketones
  138452. thioalkyl
  138453. thioalkylation
  138454. thioamide
  138455. thioamides
  138456. thioaminyl
  138457. thiobenzophenone
  138458. thioboration
  138459. thiocar
  138460. thiocarbamoyl
  138461. thiocarbenium
  138462. thiocarbonyl
  138463. thiocarbonyl
  138464. compounds
  138465. organic
  138466. synthesis
  138467. 14-addition
  138468. thiocarbonyls
  138469. thiocarboxylic
  138470. thiocarboxylic
  138471. amides
  138472. thiocarboxylic
  138473. chlorides
  138474. thiocarboxylic
  138475. o-esters
  138476. thiocarboxylic
  138477. s-ester
  138478. imides
  138479. thiocarboxylic
  138480. esters
  138481. salts
  138482. thiocarboxylic
  138483. s-esters
  138484. thiochroman
  138485. thiocoumarins
  138486. thiocyanate
  138487. thiocyanates
  138488. thiocyanidate
  138489. thiocyanidate-isothi
  138490. thiocyanidates
  138491. thiocyanogen
  138492. thiodicarboxylic
  138493. thioester
  138494. thioesters
  138495. thioether
  138496. thioethers
  138497. thiofluorenone
  138498. thioformyl
  138499. thioformyl
  138500. compounds
  138501. synthesis
  138502. structure
  138503. properties
  138504. thioformylation
  138505. thiofulminic
  138506. thiofuranosides
  138507. thiohydroxamates
  138508. thiohydroxamic
  138509. thioimide
  138510. thioisomunchnones
  138511. thioketene
  138512. thioketenes
  138513. thioketenes
  138514. their
  138515. derivatives
  138516. thioketones
  138517. thiol
  138518. thiolactams
  138519. thiolactones
  138520. thiolate
  138521. thiolates
  138522. thiolation
  138523. thiolesters
  138524. thiolo
  138525. thiols
  138526. thiols
  138527. synthons
  138528. thiols
  138529. sulfides
  138530. sulfoxides
  138531. sulfones
  138532. thiols
  138533. unsymmetrical
  138534. sulfides
  138535. thioacetals
  138536. thiomide
  138537. thionation
  138538. thionation
  138539. reactions
  138540. lawesson's
  138541. reagent
  138542. thione
  138543. thiones
  138544. thionitrites
  138545. thionitroso
  138546. thionitroso
  138547. compounds
  138548. thionitrosoarenes
  138549. thionitrosoheteroare
  138550. thionium
  138551. thionocarbonates
  138552. thionoesters
  138553. thionyl
  138554. thioorganic
  138555. thiooxophosphanes
  138556. thioph
  138557. thiophene
  138558. thiophene
  138559. derivatives
  138560. thiophene-23-dione
  138561. thiophenes
  138562. thiophenes
  138563. their
  138564. benzo
  138565. derivatives
  138566. structure
  138567. thiophenes
  138568. their
  138569. benzo
  138570. derivatives
  138571. reactivity
  138572. thiophenes
  138573. their
  138574. benzo
  138575. derivatives
  138576. synthesis
  138577. thiophenethiols
  138578. thiophenium
  138579. thiophenol
  138580. thiophenoxide
  138581. thiophens
  138582. thiophosgene
  138583. thiophosphate
  138584. thiophosphonamide-st
  138585. thiophosphoryl-stabi
  138586. thiophosphorylated
  138587. thiopropionates
  138588. thiopyrans
  138589. fused
  138590. thiopyrans
  138591. thiopyroglutamates
  138592. thiopyrylium
  138593. thiopyrylium
  138594. salts
  138595. thiinium
  138596. salts
  138597. thiosulfonate
  138598. thiosulfonates
  138599. thiosulfonates
  138600. synthesis
  138601. reactions
  138602. practical
  138603. application
  138604. thiosulfonium
  138605. thiourea
  138606. thiovinyl
  138607. thioxanthylium
  138608. thioxanthylium
  138609. salts
  138610. dibenzo
  138611. opyrylium
  138612. salts
  138613. thioxo
  138614. thioxocarbon
  138615. thirdQ
  138616. third
  138617. order
  138618. nonlinear
  138619. optical
  138620. response
  138621. organic
  138622. materials
  138623. thiyl
  138624. thoamide
  138625. thoamide
  138626. thioester
  138627. cyclopentane
  138628. synthesis
  138629. trimethylt
  138630. thomas
  138631. thomas
  138632. bessiere
  138633. synthesis
  138634. monoterpenes
  138635. thomas
  138636. cytochalasan
  138637. synthesis
  138638. macrocycle
  138639. formation
  138640. thomas
  138641. turning
  138642. points
  138643. catalysis
  138644. angew
  138645. thomas
  138646. susan
  138647. organic
  138648. synthesis
  138649. roles
  138650. boron
  138651. thompson
  138652. thompson
  138653. charles
  138654. green
  138655. diana
  138656. recent
  138657. advances
  138658. dianio
  138659. thompson
  138660. marine
  138661. natural
  138662. products
  138663. chemistry
  138664. thoms
  138665. thomson
  138666. thomson
  138667. chemistry
  138668. natural
  138669. products
  138670. thornley
  138671. those
  138672. thought
  138673. thoughts
  138674. threading
  138675. threading
  138676. molecular
  138677. strings
  138678. molecular
  138679. rings
  138680. synthesis
  138681. threads
  138682. three
  138683. three
  138684. one-half
  138685. approaches
  138686. synthesis
  138687. pederin
  138688. three
  138689. carben
  138690. homologating
  138691. agents
  138692. three
  138693. center
  138694. electron
  138695. bonds
  138696. organic
  138697. chemistry
  138698. three
  138699. component
  138700. intramolecular
  138701. alkyne
  138702. annulations
  138703. three
  138704. component
  138705. palladium
  138706. catalysed
  138707. cyclisation
  138708. carbonylatio
  138709. three-carbon
  138710. three-center
  138711. three-center
  138712. two-electron
  138713. c-h-c
  138714. bonds
  138715. organic
  138716. chemistry
  138717. three-component
  138718. three-membered
  138719. three-membered
  138720. rings
  138721. heteroatoms
  138722. fused-ring
  138723. threedimensional
  138724. threefold
  138725. threitol
  138726. threo
  138727. threo
  138728. threonine
  138729. threose
  138730. thromboxane
  138731. thromboxanes
  138732. through
  138733. reaction
  138734. centers
  138735. remote
  138736. substi
  138737. through-bond-mediate
  138738. throughbond
  138739. thummel
  138740. thummel
  138741. benzocyclobutene
  138742. related
  138743. compounds
  138744. 198013
  138745. thummel
  138746. randolph
  138747. application
  138748. friedlander
  138749. fische
  138750. thummel
  138751. randolph
  138752. synthesis
  138753. properties
  138754. organized
  138755. thurston
  138756. thurston
  138757. david
  138758. subhas
  138759. synthesisof
  138760. interactive
  138761. thyagarajan
  138762. thymefaeaceae
  138763. thymelaeaceae
  138764. thymidine
  138765. thymine
  138766. ticl4
  138767. tidwell
  138768. tidwell
  138769. sterically
  138770. crowded
  138771. organic
  138772. molecules
  138773. synthesis
  138774. tiecco
  138775. tiecco
  138776. radical
  138777. attack
  138778. substitution
  138779. aromat
  138780. tiemann
  138781. tienam
  138782. tienes
  138783. tietze
  138784. tietze
  138785. beifuss
  138786. sequential
  138787. transformations
  138788. tiffeneau-demjanov
  138789. tigliane
  138790. tilak
  138791. gogte
  138792. syntheses
  138793. rearrangements
  138794. timashev
  138795. times
  138796. timofeeva
  138797. timokhin
  138798. timokhina
  138799. timothy
  138800. timpe
  138801. organic
  138802. synthesis
  138803. effective
  138804. synthesis
  138805. enolates
  138806. aldol
  138807. michael
  138808. related
  138809. reactions
  138810. organic
  138811. synthesis
  138812. acetylides
  138813. overview
  138814. mediated
  138815. stereoselective
  138816. synthesis
  138817. epoxides
  138818. radical
  138819. addition
  138820. alkynyl
  138821. sulfides
  138822. reactivity
  138823. reagents
  138824. organic
  138825. synthesis
  138826. tin-copper
  138827. tin-copper
  138828. transmetalation
  138829. cross-coupling
  138830. a-heteroatom-su
  138831. tin-tin
  138832. tinyakova
  138833. tions
  138834. tippse-br
  138835. tipson
  138836. tiripicchio
  138837. tirthankar
  138838. tisler
  138839. tisler
  138840. stanovnik
  138841. recent
  138842. advances
  138843. pyridazine
  138844. chemistry
  138845. tissue
  138846. titaniumH
  138847. titanium
  138848. onium
  138849. derivatives
  138850. organic
  138851. synthesis
  138852. titanium
  138853. catalyzed
  138854. cascade
  138855. carboalumination
  138856. dienes
  138857. titanium
  138858. enolates
  138859. complexes
  138860. disubstituted
  138861. titanium
  138862. organic
  138863. synthesis
  138864. titanium
  138865. chloride
  138866. catalyzed
  138867. cyanation
  138868. benzylic
  138869. halides
  138870. titanium
  138871. mediated
  138872. additions
  138873. borohydride
  138874. alkenes
  138875. titanium
  138876. mediation
  138877. aldol
  138878. reactions
  138879. fridamycin
  138880. titanium
  138881. metallacycles
  138882. intermediates
  138883. synthesis
  138884. titanium
  138885. tetrachloride
  138886. organic
  138887. synthesis
  138888. titanium-alkyne
  138889. titanium-based
  138890. titanium-catalyzed
  138891. titanium-catalyzed
  138892. reductive
  138893. cyclization
  138894. e-unsaturated
  138895. titanium-catalyzed
  138896. reductive
  138897. cyclization
  138898. unsaturated
  138899. titanium-mediated
  138900. titanium-mediated
  138901. cyclizations
  138902. b-keto
  138903. esters
  138904. acetals
  138905. titanocene
  138906. tives
  138907. tiwari
  138908. tkachenko
  138909. tkhaper
  138910. tmhdiol
  138911. tmscl
  138912. tmsi-hmds
  138913. recognition
  138914. solid
  138915. state
  138916. advances
  138917. todesco
  138918. todres
  138919. todres
  138920. todres
  138921. electron
  138922. transfer
  138923. substitution
  138924. todres
  138925. electron
  138926. transfer
  138927. stage
  138928. reacti
  138929. together
  138930. togni
  138931. togni
  138932. antonio
  138933. pastor
  138934. stephen
  138935. cooperativity
  138936. chirality
  138937. togni
  138938. antonio
  138939. venanzi
  138940. luigi
  138941. nitrogen
  138942. donors
  138943. organometal
  138944. tohru
  138945. tokio
  138946. tokumaru
  138947. tokunaga
  138948. tokuno
  138949. tokuno
  138950. kenji
  138951. miyoshi
  138952. fumihisa
  138953. tsutomu
  138954. ohashi
  138955. applications
  138956. tokyo
  138957. tokyo
  138958. tolbert
  138959. tolerantz
  138960. tolkachev
  138961. tolkachev
  138962. nakova
  138963. evstigneeva
  138964. synthesis
  138965. bisben
  138966. tolman
  138967. tolstikov
  138968. tolstikov
  138969. tolstikov
  138970. glycals
  138971. enantiospecific
  138972. synth
  138973. tolstikov
  138974. borisova
  138975. cherkashin
  138976. komarov
  138977. arzam
  138978. toluene
  138979. toluenes
  138980. toluenesulfinyl
  138981. toluenesulfonate
  138982. toluenesulfonyl
  138983. toluenesulfonylhydra
  138984. toluenesulphonate
  138985. toluidines
  138986. tolylcarbene
  138987. tolylsulfinyl
  138988. tolylsulfinylacrolei
  138989. tolylsulfinylcycloal
  138990. tomalia
  138991. tomalia
  138992. donald
  138993. durst
  138994. dupont
  138995. genealogically
  138996. directed
  138997. tomalia
  138998. donald
  138999. starburst
  139000. cascade
  139001. dendrimers
  139002. fundamental
  139003. tomas
  139004. tomasik
  139005. tombo
  139006. tometsko
  139007. tomikazu
  139008. tomilov
  139009. tomilov
  139010. dokichev
  139011. dzhemilev
  139012. nefedov
  139013. catalyti
  139014. tominaga
  139015. tomioka
  139016. tomita
  139017. tomlinson
  139018. tomlinson
  139019. chandross
  139020. photochemistry
  139021. rhodopsins
  139022. tommasi
  139023. tomoda
  139024. tomoya
  139025. tonani
  139026. tonellato
  139027. toner
  139028. toniolo
  139029. toofan
  139030. toogood
  139031. tools
  139032. toomey
  139033. toone
  139034. chemistry
  139035. pseudo
  139036. sugars
  139037. suami
  139038. metal
  139039. homoenolates
  139040. siloxycyclopr
  139041. preparation
  139042. selectively
  139043. alkylated
  139044. synthesis
  139045. deoxy
  139046. oligosaccharides
  139047. synthesis
  139048. glycolipids
  139049. synthetic
  139050. saccharide
  139051. photochemistry
  139052. brief
  139053. history
  139054. photoinduced
  139055. elect
  139056. dihalocyclopropanes
  139057. organic
  139058. through
  139059. modulation
  139060. reaction
  139061. electron
  139062. transfer
  139063. processes
  139064. imagin
  139065. fundamental
  139066. concepts
  139067. photoinduced
  139068. photoinduced
  139069. electron
  139070. transfer
  139071. photoinduced
  139072. electron
  139073. transfer
  139074. oxygen
  139075. photoinduced
  139076. electron
  139077. transfer
  139078. photoinduced
  139079. electron
  139080. transfer
  139081. polyme
  139082. chemical
  139083. reactions
  139084. induced
  139085. probed
  139086. topic
  139087. topical
  139088. topically
  139089. topics
  139090. topics
  139091. topochemical
  139092. topological
  139093. topological
  139094. stereochemistry
  139095. topologically
  139096. topology
  139097. topotecan
  139098. topuzyan
  139099. topuzyan
  139100. nesunts
  139101. reactions
  139102. dihydro
  139103. torands
  139104. torbjoern
  139105. torchia
  139106. torchia
  139107. vanderhart
  139108. power
  139109. double
  139110. resonance
  139111. studi
  139112. torgasheva
  139113. torii
  139114. tormented
  139115. toromanoff
  139116. toromanoff
  139117. dynamic
  139118. stereochemistry
  139119. membere
  139120. toropova
  139121. torrance
  139122. torrance
  139123. difference
  139124. between
  139125. metallic
  139126. insulating
  139127. torroba
  139128. torsell
  139129. torsion
  139130. torsional
  139131. torsten
  139132. tortix
  139133. toshiaki
  139134. toshikazu
  139135. toshiki
  139136. toshiko
  139137. toshima
  139138. toshima
  139139. kazunobu
  139140. tatsuta
  139141. kuniaki
  139142. recent
  139143. progress
  139144. glycos
  139145. toshimasa
  139146. toshio
  139147. toshiro
  139148. toshiyasu
  139149. tosmic
  139150. tosmic
  139151. useful
  139152. synthetic
  139153. reagent
  139154. organic
  139155. chemistry
  139156. tosyl
  139157. tosylaldimines
  139158. tosylalkanoates
  139159. tosylamide
  139160. tosylated
  139161. tosylated
  139162. lithium
  139163. lithiomethyl
  139164. propen
  139165. olate
  139166. alkoxi
  139167. tosylhydrazadines
  139168. tosylhydrazones
  139169. tosyloxy
  139170. tosyloxycarbamate
  139171. tosylpropene
  139172. total
  139173. total
  139174. total
  139175. total
  139176. synthesis
  139177. determination
  139178. absolute
  139179. configurat
  139180. total
  139181. synthesis
  139182. preliminary
  139183. evaluation
  139184. duocar
  139185. total
  139186. synthesis
  139187. human
  139188. breast
  139189. tumor
  139190. associated
  139191. antigen
  139192. total
  139193. synthesis
  139194. silphiperfolane
  139195. derivative
  139196. intra
  139197. total
  139198. synthesis
  139199. altemicidin
  139200. novel
  139201. exploitation
  139202. total
  139203. synthesis
  139204. amaryllidaceae
  139205. alkaloids
  139206. 511-metha
  139207. total
  139208. synthesis
  139209. antibiotic
  139210. benzyne-furan
  139211. cycloadditi
  139212. total
  139213. synthesis
  139214. balanol
  139215. total
  139216. synthesis
  139217. balanol
  139218. designed
  139219. analogues
  139220. total
  139221. synthesis
  139222. bouvardin
  139223. o-methylbouvardin
  139224. o-methyl-
  139225. total
  139226. synthesis
  139227. brevetoxin
  139228. first
  139229. generation
  139230. strategie
  139231. total
  139232. synthesis
  139233. brevetoxin
  139234. second
  139235. generation
  139236. strategi
  139237. total
  139238. synthesis
  139239. brevetoxin
  139240. final
  139241. strategy
  139242. complet
  139243. total
  139244. synthesis
  139245. dactomelynes
  139246. total
  139247. synthesis
  139248. dactylol
  139249. novel
  139250. annulation
  139251. appro
  139252. total
  139253. synthesis
  139254. deoxypancratistatin
  139255. radical
  139256. cyclization
  139257. total
  139258. synthesis
  139259. methyl
  139260. dynamycin
  139261. methyl
  139262. total
  139263. synthesis
  139264. oxogelsemine
  139265. total
  139266. synthesis
  139267. dl-21-oxogelsemine
  139268. total
  139269. synthesis
  139270. dynemycin
  139271. total
  139272. synthesis
  139273. ebelacatone
  139274. total
  139275. synthesis
  139276. fk506
  139277. total
  139278. synthesis
  139279. ginkgolide
  139280. total
  139281. synthesis
  139282. gypsetin
  139283. total
  139284. synthesis
  139285. heliannuol
  139286. intramolecular
  139287. julia
  139288. coupl
  139289. total
  139290. synthesis
  139291. himbacine
  139292. himbelline
  139293. total
  139294. synthesis
  139295. hitachimycin
  139296. total
  139297. synthesis
  139298. indolizomycin
  139299. total
  139300. synthesis
  139301. ionophore
  139302. antibiotic
  139303. x-14547a
  139304. indanomycin
  139305. total
  139306. synthesis
  139307. lactacystin
  139308. glutamate
  139309. total
  139310. synthesis
  139311. lactone
  139312. sesquiterpenes
  139313. using
  139314. intramolecul
  139315. total
  139316. synthesis
  139317. laurencin
  139318. acetal-vinyl
  139319. sulfide
  139320. total
  139321. synthesis
  139322. leinamycin
  139323. total
  139324. synthesis
  139325. macbecin
  139326. total
  139327. synthesis
  139328. mevinolin
  139329. compactin
  139330. total
  139331. synthesis
  139332. mitomycins
  139333. total
  139334. synthesis
  139335. montanine
  139336. amaryllidaceae
  139337. alkaloids
  139338. total
  139339. synthesis
  139340. myrocin
  139341. total
  139342. synthesis
  139343. natural
  139344. ent-fredericamycin
  139345. desacetamido
  139346. total
  139347. synthesis
  139348. paeoniflorigenin
  139349. paeoniflorin
  139350. total
  139351. synthesis
  139352. paeoniflorigenin
  139353. paeoniforin
  139354. total
  139355. synthesis
  139356. paeoniflorin
  139357. total
  139358. synthesis
  139359. papuamine
  139360. stereospecific
  139361. intramolecul
  139362. total
  139363. synthesis
  139364. piperazinomycin
  139365. total
  139366. synthesis
  139367. polycarbocyclic
  139368. sesquiterpenes
  139369. survey
  139370. total
  139371. synthesis
  139372. pyripyropene
  139373. potent
  139374. orally
  139375. bioavailab
  139376. evans-tishchenko
  139377. fragm
  139378. total
  139379. synthesis
  139380. rapamycin
  139381. novel
  139382. titanium-mediated
  139383. total
  139384. synthesis
  139385. streptonigrone
  139386. total
  139387. synthesis
  139388. subergorgic
  139389. total
  139390. synthesis
  139391. sulfated
  139392. oligosacharid
  139393. total
  139394. synthesis
  139395. swinholide
  139396. hemiswinholide
  139397. total
  139398. synthesis
  139399. tantazole
  139400. total
  139401. synthesis
  139402. tautomycin
  139403. total
  139404. synthesis
  139405. taxusin
  139406. initial
  139407. toward
  139408. taxol
  139409. total
  139410. synthesis
  139411. amoryllidaceae
  139412. alkaloids
  139413. total
  139414. synthesis
  139415. angucycline
  139416. antibiotics
  139417. urdamycinone
  139418. total
  139419. synthesis
  139420. antimalarial
  139421. sesquiterpene
  139422. peroxide
  139423. total
  139424. synthesis
  139425. cembranoid
  139426. diterpene
  139427. lactone
  139428. clemeoli
  139429. total
  139430. synthesis
  139431. cembranoid
  139432. diterpene
  139433. lactone
  139434. cleomeol
  139435. total
  139436. synthesis
  139437. fk506/fkbp
  139438. complex
  139439. total
  139440. synthesis
  139441. gilvocarcins
  139442. total
  139443. synthesis
  139444. immunosuppressive
  139445. agent
  139446. discodermolid
  139447. total
  139448. synthesis
  139449. lycopodium
  139450. alkaloids
  139451. magellanine
  139452. total
  139453. synthesis
  139454. macrolide
  139455. antibiotic
  139456. rutamycin
  139457. total
  139458. synthesis
  139459. macrolide
  139460. antitumor
  139461. antibiotic
  139462. lankac
  139463. total
  139464. synthesis
  139465. novel
  139466. benzopentathiepin
  139467. varacinium
  139468. total
  139469. synthesis
  139470. phenalenone
  139471. diterpene
  139472. salvilenone
  139473. total
  139474. synthesis
  139475. spiro-o-benzoquinone
  139476. stypoldione
  139477. total
  139478. synthesis
  139479. unusual
  139480. marine
  139481. alkaloid
  139482. papuamine
  139483. total
  139484. synthesis
  139485. trehazolin
  139486. optically
  139487. active
  139488. spirocyclohep
  139489. westiellamide
  139490. totally
  139491. totleben
  139492. totowa
  139493. touchard
  139494. touchstone
  139495. toullec
  139496. tourwe
  139497. tourwe
  139498. binst
  139499. carbon
  139500. nuclear
  139501. magnetic
  139502. resonance
  139503. touster
  139504. tovinyl
  139505. toward
  139506. toward
  139507. toward
  139508. understanding
  139509. enantioselectivity
  139510. chemical
  139511. synthesis
  139512. proteins
  139513. toward
  139514. developement
  139515. general
  139516. chiral
  139517. auxiliary
  139518. towards
  139519. towards
  139520. novel
  139521. organic-synthesis
  139522. multimetallic
  139523. centers
  139524. townsend
  139525. townsend
  139526. leroy
  139527. chemistry
  139528. nucleosides
  139529. nucleotides
  139530. townsend
  139531. leroy
  139532. tipson
  139533. stuart
  139534. nucleic
  139535. chemistry
  139536. toxic
  139537. toxication
  139538. toxicities
  139539. toxicity
  139540. toxicity
  139541. heterocycles
  139542. toxicology
  139543. toxicology
  139544. organic
  139545. peroxy
  139546. compounds
  139547. toxigenic
  139548. toxin
  139549. toxins
  139550. toyota
  139551. yoshifuji
  139552. masaaki
  139553. extremely
  139554. bulky
  139555. lithium
  139556. trialk
  139557. tpapv
  139558. tetra-n-propylammoni
  139559. perruthenate
  139560. convenient
  139561. trace
  139562. tracing
  139563. tracy
  139564. traditional
  139565. trager
  139566. trahanovsky
  139567. trail
  139568. traldi
  139569. traldi
  139570. vettori
  139571. clerici
  139572. spectrometry
  139573. oxazoles
  139574. tramontini
  139575. tranfer
  139576. trans
  139577. trans
  139578. dithiane
  139579. dioxide
  139580. chiral
  139581. anion
  139582. equival
  139583. trans-12-diarylethyl
  139584. trans-12-disubstitut
  139585. trans-2021-didehydro
  139586. trans-25-disubstitut
  139587. trans-45-disubstitut
  139588. trans-a
  139589. trans-bicyclic
  139590. trans-bicyclo
  139591. trans-chelating
  139592. trans-cycloalkenes
  139593. trans-cycloalkenes
  139594. betweenanenes
  139595. molecular
  139596. toyota
  139597. yoshifuji
  139598. masaaki
  139599. extremely
  139600. bulky
  139601. lithium
  139602. trialk
  139603. trans-fused@
  139604. transfer
  139605. transformation
  139606. transformations
  139607. phosphorus-stabilise
  139608. anions
  139609. stereosele@
  139610. transition
  139611. transition
  139612. main-group
  139613. metals
  139614. cyclic
  139615. phosphazanes
  139616. transition
  139617. metal
  139618. catalyzed
  139619. strategies
  139620. synthesis
  139621. transition
  139622. metal
  139623. promoted
  139624. higher
  139625. order
  139626. cycloaddition
  139627. reactio@
  139628. transition
  139629. metals
  139630. synthesis
  139631. functionalisation
  139632. transition-metals
  139633. organic-synthesis
  139634. hydroformylation
  139635. redu@
  139636. trapping
  139637. treger
  139638. trialkylsilylperfluo
  139639. highly
  139640. reactive
  139641. silylating
  139642. agents
  139643. tribute
  139644. tricyclic
  139645. trifluoromethanesulf
  139646. triisobutylaluminium
  139647. trimethylsilylcarben
  139648. triple
  139649. trivalent
  139650. phosphorus
  139651. amides
  139652. phosphorylating
  139653. agents
  139654. troponoid@
  139655. tryk@
  139656. tsumuraya
  139657. takeshi
  139658. batcheller
  139659. scott
  139660. masamune
  139661. satoru
  139662. compoun@
  139663. tunicaminyluracil
  139664. toyota
  139665. yoshifuji
  139666. masaaki
  139667. extremely
  139668. bulky
  139669. lithium
  139670. trialk@
  139671. transacylation@
  139672. transformation@
  139673. transition
  139674. metal
  139675. catalyzed
  139676. strategies
  139677. synthesis
  139678. trimethylsilylacetyl@
  139679. turner
  139680. biocatalytic
  139681. reductions
  139682. useful
  139683. hydrolytic
  139684. enzymes
  139685. proteases
  139686. lipases
  139687. nitrilases@
  139688. vedejs@
  139689. vicarious
  139690. nucleophilic
  139691. aromatic
  139692. substitution
  139693. trapping
  139694. weisshaar@
  139695. wittig@
  139696. promoted
  139697. reactions
  139698. cyano
  139699. group
  139700. ketone
  139701. alcohol@
  139702. transacylation
  139703. transaminase
  139704. transannular
  139705. transannular
  139706. diels-alder
  139707. intramolecular
  139708. aldol
  139709. tandem
  139710. reactio
  139711. nnular
  139712. electrophilic
  139713. cyclizations
  139714. transannulation
  139715. transbenzhydrylation
  139716. transcarboxylation
  139717. transesterification
  139718. transesterifications
  139719. transferq
  139720. transfer
  139721. transfer/nickel
  139722. transfers
  139723. transfor
  139724. transform
  139725. transformation
  139726. transformation
  139727. transformation
  139728. aldehydes
  139729. alkenylboronic
  139730. esters
  139731. formations
  139732. transformations
  139733. hydroxyalkyl
  139734. selenides
  139735. aldehydes
  139736. transformations
  139737. chloroarenes
  139738. atalyzed
  139739. transition-metal
  139740. transformations
  139741. hydroxyalkyl
  139742. selenides
  139743. aldehydes
  139744. transformations
  139745. phosphorus-stabilise
  139746. anions
  139747. stereosele
  139748. transformations
  139749. phosphorus-stabilise
  139750. anions
  139751. po-activat
  139752. transformations
  139753. phosphorus-stabilise
  139754. anions
  139755. reactions
  139756. transformations
  139757. phosphorus-stabilise
  139758. anions
  139759. heterocycl
  139760. transient
  139761. transimination
  139762. transistion
  139763. transition
  139764. transition
  139765. transition
  139766. main-group
  139767. metals
  139768. cyclic
  139769. phosphazanes
  139770. transition
  139771. metal
  139772. enzyme
  139773. catalyzed
  139774. reactions
  139775. transition
  139776. metal
  139777. assisted
  139778. reactions
  139779. diazo
  139780. compounds
  139781. transition
  139782. metal
  139783. carbene
  139784. complexes
  139785. organic
  139786. synthesis
  139787. transition
  139788. metal
  139789. catalysed
  139790. rearrangement
  139791. small
  139792. organ
  139793. transition
  139794. metal
  139795. catalysis
  139796. organotin
  139797. chemistry
  139798. transition
  139799. metal
  139800. catalyzed
  139801. addition
  139802. certain
  139803. nucleophiles
  139804. transition
  139805. metal
  139806. catalyzed
  139807. annulation
  139808. reactions
  139809. palladium
  139810. transition
  139811. metal
  139812. catalyzed
  139813. chlorine
  139814. transfer
  139815. radical
  139816. cycliza
  139817. transition
  139818. metal
  139819. catalyzed
  139820. clasen
  139821. rearrangements
  139822. transition
  139823. metal
  139824. catalyzed
  139825. decomposition
  139826. diazo
  139827. trialkylsi
  139828. transition
  139829. metal
  139830. catalyzed
  139831. epoxidations
  139832. transition
  139833. metal
  139834. catalyzed
  139835. oxidation
  139836. peroxometal
  139837. transition
  139838. metal
  139839. catalyzed
  139840. reactions
  139841. organozinc
  139842. reagents
  139843. transition
  139844. metal
  139845. catalyzed
  139846. reactions
  139847. unsaturated
  139848. diazo
  139849. transition
  139850. metal
  139851. catalyzed
  139852. strategies
  139853. synthesis
  139854. transition
  139855. metal
  139856. catalyzed
  139857. synthesis
  139858. seven
  139859. membered
  139860. carbo
  139861. transition
  139862. metal
  139863. clusters
  139864. homogeneous
  139865. catalysis
  139866. transition
  139867. metal
  139868. complexes
  139869. ilylenes
  139870. silenes
  139871. disilenes
  139872. transition
  139873. metal
  139874. complexes
  139875. unsaturated
  139876. carbenes
  139877. synthesis
  139878. transition
  139879. metal
  139880. complexes
  139881. terminal
  139882. carbyne
  139883. ligands
  139884. transition
  139885. metal
  139886. diene
  139887. complexes
  139888. organic
  139889. synthesis
  139890. transition
  139891. metal
  139892. mediated
  139893. cycloaddition
  139894. reactions
  139895. alkynes
  139896. transition
  139897. metal
  139898. mediated
  139899. cycloadditions
  139900. comprehensive
  139901. organ
  139902. transition
  139903. metal
  139904. mediated
  139905. three
  139906. component
  139907. coupling
  139908. reactions
  139909. transition
  139910. metal
  139911. organometallics
  139912. synthesis
  139913. transition
  139914. metal
  139915. organometallics
  139916. organic
  139917. synthesis
  139918. transition
  139919. metal
  139920. peroxides
  139921. related
  139922. compounds
  139923. transition
  139924. metal
  139925. pi-complexes
  139926. transition
  139927. metal
  139928. promoted
  139929. acetylene
  139930. isomerisation
  139931. reactions
  139932. transition
  139933. metal
  139934. promoted
  139935. radical
  139936. reactions
  139937. organic
  139938. transition
  139939. metal
  139940. promoted
  139941. higher
  139942. order
  139943. cycloaddition
  139944. reactio
  139945. transition
  139946. metal
  139947. promoted
  139948. higher-order
  139949. cycloadditio
  139950. reaction
  139951. transition
  139952. metal
  139953. sandwiches
  139954. reservoirs
  139955. electrons
  139956. proto
  139957. transition
  139958. metal
  139959. templates
  139960. catalysts
  139961. selective
  139962. organi
  139963. transition
  139964. metal
  139965. templates
  139966. guides
  139967. cycloadditions
  139968. transition
  139969. metal-carbene
  139970. complexes
  139971. transition
  139972. metal-catalysed
  139973. reaction
  139974. organic
  139975. halides
  139976. transition
  139977. metal-catalyzed
  139978. hydroboration
  139979. additio
  139980. transition
  139981. metal-promoted
  139982. free-radical
  139983. reactions
  139984. organic
  139985. transition
  139986. metal-stabilized
  139987. carbocations
  139988. organic
  139989. synthesi
  139990. transition
  139991. metal-tin
  139992. chemistry
  139993. transition
  139994. metals
  139995. olefins
  139996. promising
  139997. personal
  139998. transition
  139999. metals
  140000. organic
  140001. synthesis
  140002. transition
  140003. metals
  140004. organic
  140005. synthesis
  140006. hydroformylation
  140007. transition
  140008. metals
  140009. organic
  140010. synthesis
  140011. principles
  140012. transit
  140013. transition
  140014. metals
  140015. synthesis
  140016. functionalization
  140017. transition
  140018. metals
  140019. synthesis
  140020. functionalisation
  140021. transition
  140022. metals
  140023. total
  140024. synthesis
  140025. transition
  140026. structures
  140027. rocarbon
  140028. pericyclic
  140029. reactions
  140030. transition-metal
  140031. transition-metal
  140032. catalyzed
  140033. silylmetallation
  140034. acetylenes
  140035. transition-metal
  140036. fluoro
  140037. compounds
  140038. containing
  140039. carbonyl
  140040. phosph
  140041. transition-metal
  140042. promoted
  140043. hydroborations
  140044. alkenes
  140045. emerging
  140046. transition-metal
  140047. radicals
  140048. chameleon
  140049. structure
  140050. catalytic
  140051. transition-metal
  140052. templates
  140053. selectivity
  140054. organic
  140055. synthe
  140056. transition-metal-car
  140057. transition-metal-cat
  140058. transition-metal-cat
  140059. epoxidations
  140060. transition-metal-med
  140061. transition-metal-med
  140062. cleavage
  140063. reactions
  140064. transition-metal-med
  140065. reactions
  140066. organic
  140067. isocyanates
  140068. transition-metals
  140069. transition-metals
  140070. organic-synthesis
  140071. annual
  140072. survey
  140073. coverin
  140074. transition-metals
  140075. organic-synthesis
  140076. hydroformylation
  140077. transition-state
  140078. transition-state
  140079. modeling
  140080. empirical
  140081. force
  140082. fields
  140083. transitionmetal
  140084. transitionmetal
  140085. coordination
  140086. chemistry
  140087. sulfoxides
  140088. transitions
  140089. transitionstate
  140090. transiton
  140091. transl
  140092. translated
  140093. translation
  140094. translocating
  140095. translocation
  140096. transmembrane
  140097. transmetalation
  140098. transmetalation
  140099. reactions
  140100. organocopper
  140101. chemistry
  140102. transmetallation
  140103. transmetallation
  140104. involving
  140105. organotin
  140106. thiolate
  140107. amide
  140108. transmission
  140109. transport
  140110. transporters
  140111. transporting
  140112. transposition
  140113. transpositiong
  140114. transpositions
  140115. trapping
  140116. trapping
  140117. trapping
  140118. evidence
  140119. dinitrospiropentene
  140120. trash
  140121. trass
  140122. trattner
  140123. travaux
  140124. traven
  140125. traven
  140126. valery
  140127. frontier
  140128. orbitals
  140129. properties
  140130. organic
  140131. traven
  140132. valery
  140133. shapakin
  140134. sergei
  140135. charge
  140136. transfer
  140137. complexes
  140138. traylor
  140139. traylor
  140140. synthetic
  140141. model
  140142. compounds
  140143. hemoproteins
  140144. 19811
  140145. traynham
  140146. traynham
  140147. substitution
  140148. radical
  140149. aromatic
  140150. treated
  140151. treatment
  140152. treatment
  140153. conjugated
  140154. azoalkenes
  140155. tosylhydraz
  140156. tredgoldK
  140157. tredgold
  140158. order
  140159. organic
  140160. films
  140161. cambridge
  140162. presK
  140163. trees
  140164. treger
  140165. treger
  140166. trehalose-based
  140167. trehazolin
  140168. tremillon
  140169. trends
  140170. trends
  140171. synthetic
  140172. carbohydrate
  140173. chemistry
  140174. trevor
  140175. tri-n-butyl
  140176. tri-n-butyl
  140177. hydride
  140178. reagent
  140179. organic
  140180. synthesis
  140181. tri-n-butylstannanes
  140182. triacetic
  140183. triad
  140184. triadenylates
  140185. triaful
  140186. triafulvalenes
  140187. trialkoxyethyllithiu
  140188. trialkyl
  140189. trialkylborane
  140190. trialkylboranes
  140191. trialkylborohydrides
  140192. trialkylborohydrides
  140193. versatile
  140194. reducing
  140195. agents
  140196. trialkylborohydrides
  140197. versatile
  140198. reducing
  140199. agents
  140200. trialkylsilane
  140201. trialkylsilyl
  140202. trialkylsilyl
  140203. perfluoroalkane
  140204. sulfonates
  140205. silylating
  140206. agent
  140207. trialkylsilylperfluo
  140208. trialkylsilylperfluo
  140209. highly
  140210. reactive
  140211. silylating
  140212. agents
  140213. trialkylstannyllithi
  140214. trialkylstannylmethy
  140215. triallylamines
  140216. trianions
  140217. trianions
  140218. regio
  140219. stereoselective
  140220. lithiation
  140221. diallyl
  140222. trianthine
  140223. triaryl
  140224. triarylcarbenium
  140225. triarylcarbenium
  140226. catalysts
  140227. mukaiyama
  140228. aldol
  140229. triaryltellurium
  140230. triaryltrifluorotell
  140231. triaryltrifluorotell
  140232. triaryltellurium
  140233. trifluoride
  140234. triarylvinyl
  140235. triaza
  140236. triazapentadienes
  140237. triazapentalenoinden
  140238. triazenes
  140239. triazine
  140240. triazines
  140241. triazinium
  140242. triazinoindoles
  140243. triazo
  140244. triazocines
  140245. triazol
  140246. triazole
  140247. triazoles
  140248. triazoles
  140249. tetrazoles
  140250. fused
  140251. six-membered
  140252. rings
  140253. triazolines
  140254. triazolium
  140255. triazolopyridines
  140256. tribactams
  140257. tribromide
  140258. tribute
  140259. tribute
  140260. tributylallenyl
  140261. tributylstannane
  140262. tributylstannyl
  140263. tributylstannylindol
  140264. tributyltin
  140265. tricarbonic
  140266. tricarbonic
  140267. derivatives
  140268. tricarbonyl
  140269. tricarbonyl
  140270. diene
  140271. complexes
  140272. synthetically
  140273. useful
  140274. proper
  140275. tricarbonyl
  140276. eta-6-arene
  140277. chromium
  140278. complexes
  140279. organic
  140280. synthe
  140281. tricarbonyliron
  140282. tricarbonyliron
  140283. lactone
  140284. complexes
  140285. organic
  140286. synthesis
  140287. tricarbonyls
  140288. tricarbonyltropylium
  140289. tricarboxylates
  140290. trichloride
  140291. trichloroacetimidate
  140292. trichloroethane
  140293. trichloroethane
  140294. organic
  140295. synthesis
  140296. trichloromethyl
  140297. trichothecanes
  140298. trichothecene
  140299. trichothecenes
  140300. tricoordinate
  140301. tricoordinnte
  140302. tricyclic
  140303. tricyclic
  140304. tricyclo
  140305. tricyclo
  140306. 2.1.0.0
  140307. pentane
  140308. derivatives
  140309. tridentate
  140310. trideoxy
  140311. trideoxyhexoses
  140312. triene
  140313. trienes
  140314. trienomycins
  140315. triesters
  140316. triethoxysilane
  140317. triethyl
  140318. triethylborane
  140319. triethylenediamine
  140320. triethylsilane
  140321. triflate
  140322. triflate-promoted
  140323. triflates
  140324. triflic
  140325. triflic
  140326. derivatives
  140327. triflones
  140328. trifluo
  140329. trifluorid
  140330. trifluoride
  140331. trifluoro
  140332. trifluoroacetate
  140333. trifluoroacetic
  140334. trifluoroacetylation
  140335. trifluoroethyl
  140336. trifluorolactic
  140337. trifluorometanesulfo
  140338. trifluoromethanesulfz
  140339. trifluoromethanesulf
  140340. trifluoromethanesulf
  140341. derivatives
  140342. trifluoromethyl
  140343. trifluoromethyl
  140344. perfluoroalkyl
  140345. derivatives
  140346. azoles
  140347. trifluoromethyl-cont
  140348. trifluoromethyl-cont
  140349. transition
  140350. metal
  140351. complexes
  140352. trifluoromethylated
  140353. trifluoromethylation
  140354. trifluoromethylation
  140355. related
  140356. reactions
  140357. organic
  140358. chemis
  140359. trifluoromethylsulfo
  140360. trifluoropropane
  140361. trifluorostyrene
  140362. triflyloxy
  140363. trifonov
  140364. trifyl
  140365. trifyl
  140366. ation
  140367. organic
  140368. synthesis
  140369. trigger
  140370. triglycerides
  140371. trihaloanilines
  140372. trihalomethyl
  140373. trihapto-allyl
  140374. triheteroatomic
  140375. triheterocarbonates
  140376. triheterocyclic
  140377. triheteromethyl
  140378. triiodoethylene
  140379. triiodoethylene
  140380. product
  140381. thermal
  140382. decomposition
  140383. triisobutylaluminium
  140384. triisobutylaluminium
  140385. triisobutylaluminum
  140386. triisopropyl
  140387. triisopropylsilaneth
  140388. triisopropylsilyl
  140389. triketones
  140390. trimer
  140391. trimerisation
  140392. trimerization
  140393. trimethoxyborohydrid
  140394. trimethyl
  140395. trimethylaluminium
  140396. trimethylaluminum
  140397. trimethylene
  140398. trimethylenebis
  140399. trimethylenemethane
  140400. trimethylenemethanes
  140401. trimethylgermyl
  140402. trimethylphenylboran
  140403. trimethylsilane
  140404. trimethylsilanethiol
  140405. trimethylsilanolate
  140406. trimethylsiloxy
  140407. trimethylsiloxyketon
  140408. trimethylsiloxymethy
  140409. trimethylsilyl
  140410. trimethylsilyl-subst
  140411. trimethylsilylazide
  140412. trimethylsilylcarben
  140413. trimethylsilylcarben
  140414. trimethylsilylcarben
  140415. trimethylsilyl
  140416. formaldehyde
  140417. trimethylsilyldiazom
  140418. trimethylsilyldiazom
  140419. versatile
  140420. synthon
  140421. organic
  140422. synthes
  140423. trimethylsilylfluoro
  140424. trimethylsilylmethyl
  140425. trimethylsilyloxy
  140426. trimethylstannyl
  140427. trimethyltin
  140428. trimethysilane
  140429. trinajstic
  140430. trinitrato
  140431. triols
  140432. triorganoboron
  140433. triorganotellurium
  140434. triorganozincates
  140435. trioxide
  140436. tripalladium
  140437. tripeptide
  140438. triphase
  140439. triphenyl
  140440. triphenylenes
  140441. triphenylmethane
  140442. triphenylphosphine
  140443. triphenylphosphine
  140444. catalyzed
  140445. isomerizations
  140446. enynes
  140447. triphenylphosphorane
  140448. triphenylphosphorany
  140449. triphenylpyrylium
  140450. triphenylsilyl
  140451. triplatinum
  140452. triple
  140453. triple
  140454. triple
  140455. bonds
  140456. small
  140457. rings
  140458. testing
  140459. limits
  140460. chemical
  140461. triple-bonded
  140462. triplet
  140463. triplets
  140464. tripodal
  140465. tripropylsilyl
  140466. triptycene
  140467. triptycenes
  140468. triquinane
  140469. triquinanes
  140470. triruthenium
  140471. pentafluorophenyl
  140472. boron
  140473. efficient
  140474. catalyst
  140475. trinitrato
  140476. paraperiodate
  140477. efficient
  140478. heterogeneo
  140479. trishomocubanes
  140480. trisubstitutedG
  140481. trisubstituted
  140482. benzoate
  140483. synthesis
  140484. carbopalladation
  140485. trisubstituted
  140486. carbenium
  140487. triterpenes
  140488. triterpenoidsW
  140489. trithianes
  140490. trithiophenes
  140491. tritium
  140492. trityl
  140493. tritylation
  140494. trivalent
  140495. trivalent
  140496. phosphorus
  140497. amides
  140498. phosphorylating
  140499. agents
  140500. triynes
  140501. trna's
  140502. trnnsformation
  140503. troev
  140504. troev
  140505. koljo
  140506. dialkyl
  140507. hydrogen
  140508. phosphonates
  140509. structures
  140510. troev
  140511. koljo
  140512. dialkyl
  140513. hydrogen
  140514. phosphonates
  140515. substitution
  140516. trofimov
  140517. trofimov
  140518. rakhmatulina
  140519. gusarova
  140520. malysheva
  140521. eleme
  140522. trofimov
  140523. reactions
  140524. acetylene
  140525. superbasic
  140526. media
  140527. trofimov
  140528. sokolyanskaya
  140529. senning
  140530. divinyl
  140531. disulfides
  140532. trofimov
  140533. boris
  140534. mikhaleva
  140535. al'bina
  140536. further
  140537. development
  140538. trofimov
  140539. boris
  140540. nedolya
  140541. strategy
  140542. synthe
  140543. trogen
  140544. trogler
  140545. tropane
  140546. aloids
  140547. tropenes
  140548. trophiles
  140549. tropical
  140550. tropolenes
  140551. tropoloisoquinoline
  140552. tropolone
  140553. tropolonic
  140554. tropone
  140555. tropones
  140556. tropono
  140557. troponoid
  140558. tropoquinone
  140559. tropsch
  140560. tropylium
  140561. trost
  140562. trost
  140563. alpha
  140564. sulfenylated
  140565. carbonyl
  140566. compounds
  140567. organic
  140568. trost
  140569. enhanced
  140570. synthetic
  140571. efficiency
  140572. towards
  140573. natural
  140574. trost
  140575. aspects
  140576. organosulfur
  140577. mediated
  140578. synthetic
  140579. trost
  140580. transition
  140581. metal
  140582. templates
  140583. selectivity
  140584. trost
  140585. barry
  140586. fleming
  140587. comprehensive
  140588. organic
  140589. synthesis
  140590. trost
  140591. barry
  140592. biological
  140593. catalysis
  140594. synthetic
  140595. efficienc
  140596. trost
  140597. barry
  140598. economy
  140599. search
  140600. synthetic
  140601. effici
  140602. trotter
  140603. trouble
  140604. troubleshooting
  140605. troupel
  140606. troxides
  140607. trozzolo
  140608. truce
  140609. tructure
  140610. peptide
  140611. synthesis
  140612. trueblood
  140613. trumper
  140614. truncated
  140615. truscheit
  140616. truscheit
  140617. frommer
  140618. junge
  140619. muller
  140620. schmidt
  140621. wingender
  140622. tryptamines
  140623. trypto
  140624. tryptophan
  140625. tryptophane
  140626. tryptophans
  140627. trytophan
  140628. trzhtsinskaya
  140629. trzhtsinskaya
  140630. abramova
  140631. imidazole
  140632. thiones
  140633. synthesis
  140634. tsang
  140635. tsang
  140636. griffin
  140637. metabolic
  140638. activation
  140639. polynuclear
  140640. tselinskii
  140641. tsil'ko
  140642. tskiyama
  140643. tsotinis
  140644. tsoungas
  140645. tsuchida
  140646. tsuchiya
  140647. tsuda
  140648. tsuge
  140649. tsuge
  140650. synthesis
  140651. heterocycles
  140652. using
  140653. heterocumulenes
  140654. tsuji
  140655. tsuji
  140656. applications
  140657. palladium
  140658. catalyzed
  140659. promoted
  140660. tsuji
  140661. organic
  140662. synthesis
  140663. palladium
  140664. compounds
  140665. springer
  140666. tsuji
  140667. palladium
  140668. catalyzed
  140669. reactions
  140670. butadiene
  140671. isopr
  140672. tsujiaki
  140673. tsukiyama
  140674. tsumuraya
  140675. tsumuraya
  140676. takeshi
  140677. batcheller
  140678. scott
  140679. masamune
  140680. satoru
  140681. compoun
  140682. tsunashima
  140683. tsunashima
  140684. cadmium
  140685. photosensitized
  140686. reactions
  140687. tsuneki
  140688. tsuneo
  140689. tsung
  140690. tsutomu
  140691. tsutsui
  140692. tsuyoshi
  140693. tsvetkov
  140694. oxygenated
  140695. flavin
  140696. intermediates
  140697. bacterial
  140698. lucifera
  140699. tuberine
  140700. tucker
  140701. tuena
  140702. tufariello
  140703. tufariello
  140704. alkaloids
  140705. nitrones
  140706. 197912
  140707. accounts
  140708. tugushi
  140709. tullock
  140710. tumer
  140711. tumor
  140712. tumour
  140713. tumour
  140714. targetted
  140715. boranes
  140716. coupling
  140717. closo
  140718. carboranes
  140719. tunable
  140720. tunable
  140721. stereoselectivity
  140722. addition
  140723. lithiothiazol
  140724. tundo
  140725. tundo
  140726. pietro
  140727. continuous
  140728. methods
  140729. organic
  140730. synthesis
  140731. tungsten
  140732. tungsten-promoted
  140733. tunicaminyluracil
  140734. tunicaminyluracil
  140735. tunicamycin
  140736. tunicamycin-v
  140737. tunichrome
  140738. tuning
  140739. tuning
  140740. reactivity
  140741. metals
  140742. rigid
  140743. ligand
  140744. envir
  140745. tunnel
  140746. tunneling
  140747. turbanova
  140748. turbanova
  140749. petrov
  140750. perfluoroalkyl
  140751. acetylenes
  140752. turchi
  140753. turchi
  140754. dewar
  140755. chemistry
  140756. oxazoles
  140757. turchi
  140758. oxazole
  140759. chemistry
  140760. review
  140761. recent
  140762. advances
  140763. turchi
  140764. oxazoles
  140765. oxazoles
  140766. chemistry
  140767. heterocyclic
  140768. turck
  140769. turck
  140770. queguiner
  140771. metalation
  140772. diazines
  140773. heterocycle
  140774. turecek
  140775. turgorins
  140776. turing
  140777. turkish
  140778. turnbull
  140779. turner
  140780. turner
  140781. steroids
  140782. reactions
  140783. partial
  140784. syntheses
  140785. turner
  140786. steroids
  140787. reactions
  140788. partial
  140789. synthesis
  140790. turner
  140791. steroids
  140792. reactions
  140793. partial
  140794. synthesis
  140795. natural
  140796. turner
  140797. biocatalytic
  140798. reductions
  140799. turner
  140800. recent
  140801. advances
  140802. enzyme
  140803. catalyzed
  140804. turning
  140805. turnover
  140806. turro
  140807. braeutler
  140808. magnetic
  140809. field
  140810. magnetic
  140811. isotope
  140812. turro
  140813. gratzel
  140814. braun
  140815. photophysical
  140816. photochemica
  140817. turro
  140818. mcvey
  140819. ramamurthy
  140820. lechtken
  140821. adiabatic
  140822. photorea
  140823. turro
  140824. ramamurthy
  140825. chemical
  140826. generation
  140827. excited
  140828. states
  140829. turro
  140830. ramamurthy
  140831. cherry
  140832. farneth
  140833. effect
  140834. turro
  140835. modern
  140836. molecular
  140837. photochemistry
  140838. benjamin/cummings
  140839. turro
  140840. nicholas
  140841. modern
  140842. molecular
  140843. photochemistry
  140844. university
  140845. tursch
  140846. tursch
  140847. braekman
  140848. daloze
  140849. kaisin
  140850. terpenoids
  140851. turuta
  140852. turuta
  140853. voishvillo
  140854. kamernetskii
  140855. microbiological
  140856. tustin
  140857. tuticorin
  140858. tutte
  140859. tvaroska
  140860. tweel
  140861. tweezers
  140862. twelfth
  140863. twenty
  140864. turner
  140865. biocatalytic
  140866. reductions
  140867. turro@
  140868. twenty-five@
  140869. fused
  140870. five-membered
  140871. rings
  140872. containing
  140873. heteroatom@
  140874. pandit
  140875. reaction
  140876. carbenes
  140877. pyrimidines
  140878. isoquin@
  140879. ultraviolet
  140880. photoelectron
  140881. studies
  140882. unstable
  140883. molecules
  140884. with@
  140885. undecenone@
  140886. unexpected
  140887. cycloaddition
  140888. between
  140889. ethyl
  140890. dimethylami@
  140891. unfunctionalized@
  140892. hidemitsu
  140893. suzukib
  140894. hitomi
  140895. nucleophilic
  140896. perfluoroalkylatio@
  140897. unsaturated
  140898. unstable@
  140899. unusual
  140900. unusual
  140901. electrophilic
  140902. aromatic
  140903. substitution
  140904. synthesis@
  140905. updated
  140906. synthesis
  140907. non-heterocycles@
  140908. benzocyclobutenes
  140909. intramolecular
  140910. diels
  140911. alder
  140912. reac@
  140913. sacrificial
  140914. anodes
  140915. electrochemical
  140916. functionalizati@
  140917. koten
  140918. asymmetric
  140919. catalysis
  140920. chiral
  140921. organocopper
  140922. varma
  140923. rajender
  140924. synthesis
  140925. oligonucleotide
  140926. analogs
  140927. twenty-five
  140928. twenty-five
  140929. years
  140930. dimethylsulfoxonium
  140931. methylide
  140932. rey's
  140933. twigg
  140934. twisted
  140935. carbon
  140936. expansion
  140937. through
  140938. cyclobutylcarbinyl
  140939. dimensional
  140940. studies
  140941. using
  140942. technique
  140943. dimensional
  140944. obtain
  140945. vicinal
  140946. proton
  140947. connectivities
  140948. directional
  140949. chain
  140950. synthesis
  140951. terminus
  140952. differentiation
  140953. fused
  140954. five-membered
  140955. heterocyclic
  140956. rings
  140957. classical
  140958. syste
  140959. fused
  140960. five-membered
  140961. heterocyclic
  140962. rings
  140963. non-classical
  140964. fused
  140965. five-membered
  140966. heterocyclic
  140967. rings
  140968. lambda4-
  140969. fused
  140970. five-membered
  140971. rings
  140972. containing
  140973. heteroatom
  140974. syntheses
  140975. manoalide
  140976. heteroatom
  140977. assisted
  140978. alkyne
  140979. types
  140980. stereocontrol
  140981. formation
  140982. spiro
  140983. skeleto
  140984. two-carbon
  140985. two-carbon
  140986. elongation/annulatio
  140987. alcohols
  140988. nitriles
  140989. two-directional
  140990. two-directional
  140991. chain
  140992. synthesis
  140993. terminus
  140994. differentiation
  140995. two-electron
  140996. two-metal
  140997. two-metal
  140998. catalyst
  140999. system
  141000. redox
  141001. isomerization
  141002. proparg
  141003. two-phase
  141004. twofold
  141005. tyler
  141006. tyler
  141007. david
  141008. electron
  141009. organometallic
  141010. adducts
  141011. accts
  141012. tylonolide
  141013. tylosin
  141014. tyltin
  141015. tyman
  141016. tyman
  141017. isoprenoid
  141018. chain
  141019. phenols
  141020. typed
  141021. types
  141022. tyuleneva
  141023. tyuleneva
  141024. rokhlin
  141025. knunyants
  141026. fluorine
  141027. containing
  141028. tyutin
  141029. pandit
  141030. reaction
  141031. carbenes
  141032. pyrimidines
  141033. isoquin
  141034. dzhemilev
  141035. 0rganomet
  141036. homogeneous
  141037. dzhemilev
  141038. zirconium
  141039. compl
  141040. dzhemilev
  141041. vostrikova
  141042. ibragimov
  141043. schmidt
  141044. syntheses
  141045. interconversions
  141046. alpha
  141047. mercapto
  141048. schollkopf
  141049. recent
  141050. applieations
  141051. alpha
  141052. metalated
  141053. isocyani
  141054. uccello
  141055. uchida
  141056. uchiyama
  141057. uddin
  141058. udenaite
  141059. udodong
  141060. mitsuru
  141061. direct
  141062. polycondensation
  141063. synlett
  141064. uemura
  141065. uemura
  141066. motokazu
  141067. chiral
  141068. arene
  141069. chromium
  141070. complexes
  141071. organi
  141072. uggeri
  141073. component
  141074. synthesis
  141075. peptides
  141076. specia
  141077. bauer
  141078. johannes
  141079. klemens
  141080. dengler
  141081. dietz
  141082. andre
  141083. uhlmann
  141084. ukharov
  141085. ul'ev
  141086. ul'ev
  141087. shtefan
  141088. vvedenskii
  141089. thiophenethiols
  141090. uleine
  141091. ulendeeva
  141092. ullmann
  141093. ullrich
  141094. ullrich
  141095. brugger
  141096. prostacyclin
  141097. thromboxane
  141098. synthase
  141099. ullrich
  141100. cytochrome
  141101. biological
  141102. hydroxylation
  141103. react
  141104. ulrich
  141105. ultimat
  141106. ultimate
  141107. ultimately
  141108. ultimatereagents
  141109. ultrasonic
  141110. ultrasonics
  141111. ultrasonics
  141112. organoborane
  141113. chemistry
  141114. powerful
  141115. method
  141116. ultrasound
  141117. ultrasound
  141118. pressure
  141119. microwave
  141120. heating
  141121. organic
  141122. ultrasound
  141123. organic
  141124. synthesis
  141125. ultrasound
  141126. synthesis
  141127. ultrasound
  141128. chemical
  141129. physical
  141130. biological
  141131. effects
  141132. ultraviolet
  141133. ultraviolet
  141134. photoelectron
  141135. studies
  141136. unstable
  141137. molecules
  141138. umberto
  141139. umemoto
  141140. umemoto
  141141. teruo
  141142. recent
  141143. development
  141144. fluorinating
  141145. agents
  141146. umezawa
  141147. umezawa
  141148. recent
  141149. chemical
  141150. studies
  141151. bioactive
  141152. microbial
  141153. umpoled
  141154. umpoled
  141155. synthons
  141156. survey
  141157. sources
  141158. synthesis
  141159. umpolung
  141160. umpolung
  141161. amine
  141162. reactivity
  141163. nucleophilic
  141164. alpha
  141165. secondary
  141166. umpolung
  141167. ketones
  141168. radical
  141169. cations
  141170. umpolung
  141171. reactivity
  141172. carbonyl
  141173. compounds
  141174. through
  141175. sulfur
  141176. umpolung
  141177. reactivity
  141178. carbonyl
  141179. compounds
  141180. through
  141181. umsaturated
  141182. unactivated
  141183. unambiguous
  141184. unappreciated
  141185. uncatalyzed
  141186. uncharged
  141187. unchelated
  141188. uncommon
  141189. unconventional
  141190. undecan
  141191. undecan-11-one
  141192. undecane
  141193. undecanes
  141194. undecenone
  141195. underE
  141196. underberg
  141197. understanding
  141198. understanding
  141199. controlling
  141200. diastereofacial
  141201. selectivity
  141202. underutilized
  141203. undheim
  141204. undheim
  141205. novel
  141206. dihydrothiazolo
  141207. pyridinium
  141208. olate
  141209. undheim
  141210. kjell
  141211. benneche
  141212. metalation
  141213. metal
  141214. assisted
  141215. undirected
  141216. unexpected
  141217. cycloaddition
  141218. between
  141219. ethyl
  141220. dimethylami
  141221. unexpected
  141222. arylation
  141223. tertiary
  141224. propargylic
  141225. alcohols
  141226. during
  141227. unexpected
  141228. course
  141229. darzens
  141230. reaction
  141231. phenyl
  141232. esters
  141233. unexpected
  141234. outcome
  141235. reaction
  141236. sugar
  141237. lactones
  141238. unfunctionalised
  141239. unfunctionalized
  141240. ungemach
  141241. ungemach
  141242. spiroindolenine
  141243. intermediate
  141244. revie
  141245. unger
  141246. unger
  141247. chemistry
  141248. biological
  141249. significance
  141250. unified
  141251. unimetal
  141252. unimetal
  141253. super
  141254. bases
  141255. unimolecular
  141256. union
  141257. unique
  141258. unitf
  141259. united
  141260. united
  141261. strategy
  141262. alkaloids
  141263. yohimb
  141264. units
  141265. univK
  141266. universe
  141267. university
  141268. unknown
  141269. unnamed
  141270. unnatural
  141271. hidemitsu
  141272. suzukib
  141273. hitomi
  141274. nucleophilic
  141275. perfluoroalkylatio
  141276. unpaired
  141277. unprecedented
  141278. unprecedented
  141279. rearrangement
  141280. benzoyl
  141281. substituted
  141282. bicycli
  141283. unprecidented
  141284. unprecidented
  141285. nucleophilic
  141286. addition
  141287. organolithiums
  141288. unraveling
  141289. unrelated
  141290. unsat
  141291. unsaturate
  141292. unsaturated
  141293. unsaturated
  141294. unsaturated
  141295. carbenes
  141296. unsaturated
  141297. carbenes
  141298. review
  141299. unsaturated
  141300. dimetal
  141301. cyclopentadienyl
  141302. carbonyl
  141303. complexes
  141304. unsaturated
  141305. lactones
  141306. synthesis
  141307. applications
  141308. unsaturated
  141309. silicon
  141310. alcohols
  141311. glycols
  141312. ethers
  141313. acetals
  141314. unsolved
  141315. unstabilized
  141316. unsubstituted
  141317. unsymetrical
  141318. unsymmetric
  141319. unsymmetrical
  141320. unsymmetrically
  141321. unsymmetrization
  141322. unturned
  141323. unusual
  141324. unusual
  141325. unusual
  141326. anti-selective
  141327. reduction
  141328. a-methyl
  141329. b-alkylketo
  141330. aromatic
  141331. series
  141332. unusual
  141333. isomerization
  141334. under
  141335. lawesson
  141336. thiation
  141337. conditions
  141338. unusual
  141339. molecules-unusual
  141340. reactions
  141341. tetra-tert-butyltet
  141342. unusual
  141343. properties
  141344. phosphorus
  141345. functions
  141346. 7-phosphan
  141347. unusual
  141348. reaction
  141349. nitrones
  141350. diazoles
  141351. unusual
  141352. rhodium
  141353. promoted
  141354. reaction
  141355. vinylcyclopropene
  141356. unusual
  141357. saturated
  141358. hydrocarbons
  141359. interaction
  141360. between
  141361. theoretic
  141362. unusually
  141363. unusually
  141364. facile
  141365. oxathioacetal
  141366. transfer
  141367. reaction
  141368. efficien
  141369. unverzagt
  141370. unverzagt
  141371. carlo
  141372. sugar
  141373. based
  141374. designer
  141375. against
  141376. influenz
  141377. uozumi
  141378. up-scaling
  141379. up-scaling
  141380. photochemical
  141381. reactions
  141382. update
  141383. updated
  141384. updated
  141385. updates
  141386. upendra
  141387. upper
  141388. urabe
  141389. uracil
  141390. uracils
  141391. uracils
  141392. versatile
  141393. starting
  141394. materials
  141395. heterocyclic
  141396. synthes
  141397. urans
  141398. urated
  141399. urban
  141400. urbanski
  141401. urdamycinone
  141402. ureas
  141403. uridine
  141404. uronate
  141405. uronic
  141406. uroporphyrinogen
  141407. ursula
  141408. usalysis
  141409. synthesis
  141410. non-heterocycles
  141411. 111333
  141412. hexamethyldisilazane
  141413. trimethylsily
  141414. activation
  141415. methods
  141416. organozinc
  141417. reagents
  141418. intramolecular
  141419. dipolar
  141420. nitrone
  141421. cycloaddition
  141422. azadienes
  141423. diels
  141424. alder
  141425. reaction
  141426. heterocycli
  141427. benzocyclobutenes
  141428. intramolecular
  141429. diels
  141430. alder
  141431. carbonyl
  141432. derivatives
  141433. heterocyclic
  141434. synthesis
  141435. cyclopropanes
  141436. their
  141437. derivatives
  141438. organic
  141439. synthe
  141440. cyclopropanes
  141441. their
  141442. organic
  141443. synthesis
  141444. diazo
  141445. ketone
  141446. alkoxy
  141447. alkyne
  141448. reaction
  141449. total
  141450. synthesi
  141451. dioxiranes
  141452. chemoselective
  141453. oxidation
  141454. tertia
  141455. enzymatic
  141456. aldol
  141457. reactions
  141458. synthesis
  141459. naked
  141460. fluoride
  141461. reagents
  141462. desilylation
  141463. review
  141464. nitro
  141465. acetonitriles
  141466. carbon
  141467. participant
  141468. optically
  141469. active
  141470. naphthylethyl
  141471. amine
  141472. resolution
  141473. organoiron
  141474. compounds
  141475. organic
  141476. synthesis
  141477. organonick
  141478. compounds
  141479. organic
  141480. synthesis
  141481. organorhodium
  141482. compounds
  141483. organic
  141484. synthesis
  141485. organosilicon
  141486. reagents
  141487. protective
  141488. groups
  141489. organi
  141490. pseudoephedine
  141491. practical
  141492. chiral
  141493. auxilary
  141494. sacrificial
  141495. anodes
  141496. electrochemical
  141497. functionalizati
  141498. samarium
  141499. diiodide
  141500. alternative
  141501. sodium/mercury
  141502. silicone
  141503. organic
  141504. synthesis
  141505. sodium
  141506. acetylide
  141507. organic
  141508. synthesis
  141509. sodium
  141510. acetylide
  141511. organic
  141512. synthesis
  141513. review
  141514. cover
  141515. soluble
  141516. magnesium
  141517. anthracene
  141518. reagent
  141519. initiate
  141520. basis
  141521. gausian
  141522. calculations
  141523. organic
  141524. substituted
  141525. 3-sulfolenes
  141526. precursors
  141527. 13-butadie
  141528. butyl
  141529. hydroperoxide
  141530. oxygenations
  141531. olefins
  141532. mitsunobu
  141533. reaction
  141534. synthesis
  141535. polyamines
  141536. tosmic
  141537. organic
  141538. synthesis
  141539. leading
  141540. tosmic
  141541. reagent
  141542. heterocyclic
  141543. synthesis
  141544. transition
  141545. metals
  141546. organic
  141547. synthesis
  141548. review
  141549. transition
  141550. organometallic
  141551. compounds
  141552. heterocyclic
  141553. water-soluble
  141554. ligands
  141555. homogeneous
  141556. catalysis
  141557. zeolites
  141558. organic
  141559. reactions
  141560. usefu
  141561. useful
  141562. useful
  141563. designs
  141564. synthesis
  141565. trans-fused
  141566. polyether
  141567. ser's
  141568. bromotrimethylsilane
  141569. iodotrimethylsilane
  141570. fries
  141571. rearrangement
  141572. preparation
  141573. hydro
  141574. usingF
  141575. using
  141576. using
  141577. khina
  141578. voronkov
  141579. thioformyl
  141580. compounds
  141581. ustenko
  141582. ustus
  141583. usuki
  141584. usyatinskii
  141585. utilisation
  141586. utilisation
  141587. oxygen
  141588. specific
  141589. oxidation
  141590. organic
  141591. utility
  141592. utility
  141593. utility
  141594. cyanoacetamide
  141595. heterocyclic
  141596. synthesis
  141597. utility
  141598. highly
  141599. electrophili
  141600. peroxides
  141601. functionalizati
  141602. utility
  141603. unsaturated
  141604. nitriles
  141605. heterocyclic
  141606. synthesis
  141607. utilization
  141608. zation
  141609. dimethyl
  141610. butylspiro
  141611. utilization
  141612. serine
  141613. oxime
  141614. olefin
  141615. cycloaddition
  141616. utilization
  141617. me3sisnbu3
  141618. organic
  141619. synthesis
  141620. reaction
  141621. utilizing
  141622. utimoto
  141623. utitlity
  141624. utlilizing
  141625. utrecht
  141626. uumberto
  141627. uzlova
  141628. uznanski
  141629. amarnath
  141630. broom
  141631. chemical
  141632. synthesis
  141633. oligonucleoti
  141634. amarnath
  141635. madhav
  141636. synthesis
  141637. survey
  141638. metho
  141639. mochalin
  141640. porschnev
  141641. advances
  141642. chemistry
  141643. ermakova
  141644. arsenor
  141645. cherkashin
  141646. kisilitsa
  141647. platonov
  141648. yakobson
  141649. synthesis
  141650. applica
  141651. andrianov
  141652. eremeev
  141653. heterocycl
  141654. compds
  141655. granik
  141656. zhidkova
  141657. glushkov
  141658. acetals
  141659. amides
  141660. kelarev
  141661. shvekhgeimer
  141662. heterocycl
  141663. compounds
  141664. nowlan
  141665. tidwell
  141666. structural
  141667. effects
  141668. pogorelyi
  141669. hydrogen
  141670. bonds
  141671. russian
  141672. chemic
  141673. kampars
  141674. neilands
  141675. electron
  141676. affinities
  141677. organic
  141678. karnojitzky
  141679. autooxidation
  141680. compounds
  141681. rusinov
  141682. petrov
  141683. chupakhin
  141684. heterocycl
  141685. gryaznov
  141686. smirnov
  141687. ovrutskii
  141688. protsenko
  141689. azirine
  141690. chemistry
  141691. heter
  141692. ramamurthy
  141693. venkatesan
  141694. photochem
  141695. ramamurthy
  141696. tetrahedron
  141697. 0rganic
  141698. photochemistry
  141699. petrosyan
  141700. spectra
  141701. structures
  141702. organotin
  141703. compou
  141704. simanek
  141705. preininger
  141706. pseudobase
  141707. formation
  141708. quatern
  141709. orekhov
  141710. reactions
  141711. organic
  141712. compounds
  141713. higher
  141714. fluor
  141715. pochinok
  141716. condensed
  141717. tetra
  141718. v2cl3
  141719. vacuum
  141720. vadapalli
  141721. vahrenkamp
  141722. vahrenkamp
  141723. heinrich
  141724. ligand
  141725. sphere
  141726. reactivity
  141727. organometall
  141728. vaillancourt
  141729. vainer
  141730. vaisberg
  141731. vaisman
  141732. valdes
  141733. valence
  141734. valence-bond
  141735. valent
  141736. valent-titanium
  141737. valentine
  141738. valentine
  141739. asymmetric
  141740. synthesis
  141741. synthesis
  141742. valerie
  141743. valerii
  141744. valerij
  141745. valerolactone
  141746. valerolactone
  141747. annulation
  141748. application
  141749. total
  141750. synthesis
  141751. valery
  141752. validation
  141753. validity
  141754. valko
  141755. vallee
  141756. vallee
  141757. yannick
  141758. applications
  141759. flash
  141760. vacuum
  141761. thermolysis
  141762. valley
  141763. valois
  141764. valters
  141765. valuable
  141766. values
  141767. synthesis
  141768. oligoribonucleotides
  141769. phosphotr
  141770. broek
  141771. vermaas
  141772. heskamp
  141773. boeckel
  141774. auweraer
  141775. schryver
  141776. verbeek
  141777. helsen
  141778. modifying
  141779. reactions
  141780. pyrimidines
  141781. anrorc
  141782. mechanism
  141783. mechanism
  141784. steen
  141785. koten
  141786. gerard
  141787. syntheses
  141788. amino
  141789. dienst
  141790. bakker
  141791. wouter
  141792. iwema
  141793. engbersen
  141794. johan
  141795. doorn
  141796. verboom
  141797. willem
  141798. reinhoudt
  141799. david
  141800. molecular
  141801. koten
  141802. asymmetric
  141803. catalysis
  141804. chiral
  141805. organocopper
  141806. koten
  141807. vrieze
  141808. interaction
  141809. metal
  141810. centres
  141811. verboom
  141812. reinhoudt
  141813. selective
  141814. functionaliza
  141815. veggel
  141816. frank
  141817. verboom
  141818. willem
  141819. reinhoudt
  141820. david
  141821. vanadium
  141822. vanadium
  141823. peroxide
  141824. complexes
  141825. vance
  141826. vancomycin
  141827. vanderhart
  141828. vanderwaals
  141829. vandewalle
  141830. vanishing
  141831. vapor
  141832. vapors
  141833. varacin
  141834. varacinium
  141835. varezhkin
  141836. varfolomeev
  141837. varfolomeev
  141838. rainina
  141839. lozinskii
  141840. cryoimmobilized
  141841. vargas
  141842. variable
  141843. variant
  141844. variation
  141845. variations
  141846. varied
  141847. varieties
  141848. variety
  141849. varinder
  141850. various
  141851. various
  141852. nucleophilic
  141853. aromatic
  141854. substitution
  141855. trapping
  141856. variously
  141857. varlamov
  141858. varma
  141859. varma
  141860. rajender
  141861. synthesis
  141862. oligonucleotide
  141863. analogs
  141864. varnaeva
  141865. varney
  141866. vartanyan
  141867. varvoglis
  141868. varvoglis
  141869. anastassios
  141870. organic
  141871. chemistry
  141872. polycoordinat
  141873. varying
  141874. vasella
  141875. vasella
  141876. andrea
  141877. approach
  141878. synthesis
  141879. glycosides
  141880. vasella
  141881. andrea
  141882. reactions
  141883. intermediates
  141884. involving
  141885. vasil'ev
  141886. vasil'eva
  141887. vasilevskii
  141888. vassilev
  141889. vassilios
  141890. vasuari
  141891. vasvari
  141892. vatives
  141893. vaughan
  141894. vaughan
  141895. stevens
  141896. monoalkyltriazenes
  141897. chemic
  141898. vaupel
  141899. vazquez
  141900. vdorin
  141901. vedejs
  141902. vedejs
  141903. vedejs
  141904. peterson
  141905. stereochemistry
  141906. mechanism
  141907. vedeneev
  141908. veenstra
  141909. veeraraghavan
  141910. vegetable
  141911. veggel
  141912. vehicle
  141913. vehicles
  141914. veillard
  141915. veillard
  141916. alain
  141917. initio
  141918. calculations
  141919. transition
  141920. metal
  141921. veinberg
  141922. veinberg
  141923. lukevics
  141924. organosilicon
  141925. organotin
  141926. compound
  141927. veith
  141928. velarde
  141929. velden
  141930. veldhuizen
  141931. velichko
  141932. vellaccio
  141933. vellekoop
  141934. veltheer
  141935. venanzi
  141936. venepalli
  141937. venkataraghavan
  141938. venkataramu
  141939. venkatesan
  141940. ventures
  141941. veratrole
  141942. veratrum
  141943. verbacine
  141944. verbaskine
  141945. verbeek
  141946. verboom
  141947. verdazyl
  141948. verdine
  141949. vereshchagin
  141950. vereshechagin
  141951. vergeychik
  141952. verhe
  141953. verhoeven
  141954. verhoeven
  141955. scherer
  141956. willemse
  141957. solvent
  141958. effects
  141959. vedejs
  141960. verbascenine@
  141961. verhoeven
  141962. sigma
  141963. assistance
  141964. modulation
  141965. intramolecu@
  141966. vernon
  141967. versatile
  141968. methylenecyclopentan
  141969. annulations
  141970. unactivate@
  141971. versitile
  141972. viability@
  141973. ylcopper@
  141974. vinylidenecyclopropa@
  141975. viola
  141976. collins
  141977. filipp
  141978. intramolecular
  141979. pericyclic
  141980. react@
  141981. aryku
  141982. ozonolytic
  141983. transformations
  141984. labdane
  141985. vogtle
  141986. rossa
  141987. pyrolysis
  141988. sulfones
  141989. synthetic
  141990. method@
  141991. volume
  141992. vuorinen@
  141993. durckheimer
  141994. blumbach
  141995. lattrell
  141996. scheunemann
  141997. ange@
  141998. speckamp
  141999. hiemstra
  142000. tetrahedron
  142001. intramo@
  142002. wada@
  142003. waichiro@
  142004. peter
  142005. shukla
  142006. deepak
  142007. utility
  142008. behavior
  142009. warwel
  142010. siegfried
  142011. sojka
  142012. michael
  142013. rusch
  142014. klaas
  142015. synthesi@
  142016. watson
  142017. wehrli
  142018. nishida
  142019. natural
  142020. products
  142021. verhoeven
  142022. sigma
  142023. assistance
  142024. modulation
  142025. intramolecu
  142026. verification
  142027. verkhovskaya
  142028. verkhovskaya
  142029. yamskov
  142030. enzymic
  142031. methods
  142032. resolving
  142033. verlag
  142034. verlagsgesellschaft
  142035. verley
  142036. vermaas
  142037. vernin
  142038. vernon
  142039. vernon
  142040. veronique
  142041. verpoorte
  142042. verpoorte
  142043. robert
  142044. heiden
  142045. robert
  142046. gulik
  142047. walter
  142048. versatile
  142049. methylenecyclopentan
  142050. annulations
  142051. unactivate
  142052. versatile
  142053. roles
  142054. lewis
  142055. acids
  142056. reactions
  142057. allylic
  142058. versatility
  142059. version
  142060. versitile
  142061. versitile
  142062. verstegen
  142063. versus
  142064. vertebrate
  142065. verweij
  142066. verweij
  142067. vroom
  142068. industrial
  142069. transformations
  142070. veschambres
  142071. veselov
  142072. veselovskii
  142073. vesicles
  142074. vessiere
  142075. vesterhoff
  142076. vettori
  142077. ional
  142078. vibrations
  142079. vic-bis
  142080. vicarious
  142081. vicarious
  142082. nucleophilic
  142083. aromatic
  142084. substitution
  142085. trapping
  142086. vicarious
  142087. nucleophilic
  142088. substitution
  142089. hydrogen
  142090. chemi
  142091. vicens
  142092. vicente
  142093. vicinal
  142094. vicinally-substitute
  142095. vicinity
  142096. vicinol
  142097. vicinol
  142098. cyclic
  142099. thionocarbonates
  142100. cyclic
  142101. sulfates
  142102. vicky
  142103. victor
  142104. victoria
  142105. vidya
  142106. viehe
  142107. viehe
  142108. merenyi
  142109. stella
  142110. janousek
  142111. capto
  142112. dative
  142113. substit
  142114. vienna
  142115. views
  142116. vigabatrin
  142117. vigabatrin
  142118. synthesis
  142119. thermal
  142120. rearrangements
  142121. vigato
  142122. vil'davskaya
  142123. viliam
  142124. vilkov
  142125. villani
  142126. villiger
  142127. villiger
  142128. vilsmaier
  142129. vilsmeier
  142130. vilsmeier-haack
  142131. vinader
  142132. vinamidinium
  142133. vinayak
  142134. vinblastine
  142135. vinca
  142136. vincamine
  142137. vincent
  142138. vincenti
  142139. vincenti
  142140. marco
  142141. pelizzetti
  142142. dalcanale
  142143. enrico
  142144. soncini
  142145. vincenzo
  142146. vineomycinone
  142147. vinhlastine
  142148. vining
  142149. vinnik
  142150. vinod
  142151. vinogradov
  142152. vinogradova
  142153. vinylC
  142154. vinyl
  142155. vinyl
  142156. acetals
  142157. related
  142158. compounds
  142159. organic
  142160. synthesis
  142161. vinyl
  142162. cations
  142163. vinyl
  142164. alkoxy
  142165. radicals
  142166. organic
  142167. synthesis
  142168. vinyl
  142169. anion
  142170. acetylide
  142171. equivalents
  142172. functions
  142173. vinyl
  142174. boranes
  142175. trans
  142176. dihydroxyethylene
  142177. equivalents
  142178. vinyl
  142179. carboxylate
  142180. acylating
  142181. reagent
  142182. selective
  142183. acylati
  142184. vinyl
  142185. cations
  142186. vinyl
  142187. radical
  142188. based
  142189. cyclization
  142190. substituted
  142191. deoxy
  142192. vinyl
  142193. substitutions
  142194. organopalladium
  142195. intermediates
  142196. vinyl
  142197. tellur
  142198. synthesis
  142199. properties
  142200. vinyl
  142201. triflate
  142202. chemistry
  142203. unsaturated
  142204. cations
  142205. carbenes
  142206. vinylacetylenes
  142207. vinylacrylic
  142208. vinylalkylidene
  142209. vinylallenes
  142210. vinylarenes
  142211. vinylation
  142212. vinylation
  142213. indole
  142214. position
  142215. palladium
  142216. catalyzed
  142217. vinylaziridenes
  142218. vinylcarbene
  142219. vinylcarbenoids
  142220. vinylcopper
  142221. vinylcycloalkenes
  142222. vinylcyclobutanol
  142223. vinylcyclohexanols
  142224. vinylcyclopropane
  142225. vinylcyclopropane
  142226. rearrangement
  142227. ethyl
  142228. ethenylbicyclo
  142229. vinylcyclopropane
  142230. rearrangements
  142231. vinylcyclopropane
  142232. rearrangements
  142233. organic
  142234. synthesis
  142235. vinylcyclopropane-cy
  142236. vinylcyclopropanesD
  142237. vinylcyclopropene
  142238. vinylcycopentane
  142239. vinyldiazomethanes
  142240. vinylene
  142241. vinylhydroxylamine
  142242. vinylic
  142243. vinylic
  142244. arylic
  142245. oxidation
  142246. vinylic
  142247. selenides
  142248. vinylic
  142249. substitution
  142250. vinyl
  142251. tellurides
  142252. cuprates
  142253. vinylic
  142254. tellurides
  142255. precursors
  142256. vinyllithium
  142257. vinylcoppe
  142258. vinylictellurides
  142259. vinyliden
  142260. vinylidene
  142261. vinylidene
  142262. allenylidene
  142263. metal
  142264. complexes
  142265. vinylidenecyclopropa
  142266. vinylidenes
  142267. vinylidenes
  142268. intermediates
  142269. thermal
  142270. cyclopropene
  142271. vinylimino
  142272. vinylindole
  142273. vinylindoles
  142274. vinylketenes
  142275. vinylketenimines
  142276. vinyllithium
  142277. vinyllithium
  142278. dynamic
  142279. behavior
  142280. tetrahydrofuran
  142281. solution
  142282. vinylmetals
  142283. vinylmorpholine
  142284. vinylogous
  142285. vinylogs
  142286. vinylogues
  142287. vinyloxirane
  142288. vinyloxiranes
  142289. vinylph
  142290. vinylphosphonates
  142291. vinylphosphonates
  142292. organic
  142293. synthesis
  142294. vinylphosphonium
  142295. vinylsilane
  142296. vinylsilane-and
  142297. vinylsilane-and
  142298. alkynylsilane-termin
  142299. cyclisation
  142300. reactions
  142301. vinylsilanes
  142302. vinylstannanes
  142303. vinylstannyl
  142304. vinylsulfoxyallenes
  142305. vinylthionium
  142306. vinyltrimethylstanna
  142307. vinylzirconation
  142308. viola
  142309. viola
  142310. collins
  142311. filipp
  142312. intramolecular
  142313. pericyclic
  142314. react
  142315. violations
  142316. violations
  142317. hund's
  142318. kekule
  142319. hydrocarbons
  142320. theoret
  142321. violet
  142322. viologens
  142323. viqar
  142324. viridine
  142325. virtually
  142326. virtually
  142327. complete
  142328. blocking
  142329. unsaturated
  142330. aldehyde
  142331. virtually
  142332. complete
  142333. blocking
  142334. b-unsaturated
  142335. aldehyde
  142336. virtue
  142337. viscosity
  142338. visentin
  142339. vision
  142340. vismara
  142341. visser
  142342. visser
  142343. herman
  142344. reinhoudt
  142345. david
  142346. feike
  142347. carrier
  142348. vista
  142349. vistas
  142350. visual
  142351. vitaminm
  142352. vitamin-d
  142353. vitamins
  142354. vitorio
  142355. vitro
  142356. vivona
  142357. vivona
  142358. nicolo
  142359. buscemi
  142360. silvestre
  142361. frenna
  142362. vincenzo
  142363. cusmano
  142364. aryku
  142365. ozonolytic
  142366. transformations
  142367. labdane
  142368. vladimir
  142369. vladmmir
  142370. vladuchick
  142371. vlasov
  142372. vlasov
  142373. fluoride
  142374. nucleophile
  142375. leaving
  142376. group
  142377. vlasta
  142378. vlastimil
  142379. vliegenihari
  142380. vliegenthart
  142381. vliegenthart
  142382. enzymic
  142383. enzymic
  142384. oxidation
  142385. vocabulary
  142386. voegelein
  142387. voegtle
  142388. voegtle
  142389. fritz
  142390. knops
  142391. peter
  142392. pigments
  142393. visual
  142394. differentiatio
  142395. voelter
  142396. voelter
  142397. stoeva
  142398. kaiser
  142399. grubler
  142400. mihelic
  142401. echner
  142402. vogel
  142403. vogel
  142404. bridged
  142405. annulenes
  142406. israel
  142407. journal
  142408. vogel
  142409. emanuel
  142410. porphyrins
  142411. annulene
  142412. chemist's
  142413. vogtle
  142414. vogtle
  142415. fascinating
  142416. molecules
  142417. organic
  142418. chemistry
  142419. vogtle
  142420. hohner
  142421. multibridged
  142422. multilayered
  142423. multistepped
  142424. vogtle
  142425. rossa
  142426. pyrolysis
  142427. sulfones
  142428. synthetic
  142429. method
  142430. vogtle
  142431. sieger
  142432. muller
  142433. complexation
  142434. uncharged
  142435. molec
  142436. vogtle
  142437. supramolecular
  142438. chemistry
  142439. introduction
  142440. wiley
  142441. vogtle
  142442. weber
  142443. multidentate
  142444. acyclic
  142445. neutral
  142446. ligands
  142447. voishvillo
  142448. voitsekhovskii
  142449. vol'kenshtein
  142450. vol'pim
  142451. vol'pin
  142452. volatile
  142453. volke
  142454. volke
  142455. liska
  142456. electrochemistry
  142457. organic
  142458. synthesis
  142459. spring
  142460. volker
  142461. volkov
  142462. volkov
  142463. immunoassay
  142464. alkaloids
  142465. russian
  142466. chemical
  142467. reviews
  142468. volkova
  142469. vollhardt
  142470. vollhardt
  142471. peter
  142472. phenylenes
  142473. applied
  142474. chemistr
  142475. vollherdt
  142476. volmer
  142477. volodarskii
  142478. volodarskyJ
  142479. volodarsky
  142480. reznikov
  142481. ovcharenko
  142482. synthetic
  142483. chemistJ
  142484. volodarsky
  142485. leonid
  142486. reznikov
  142487. vladimir
  142488. ovcharenko
  142489. victor
  142490. volume
  142491. volume
  142492. volume
  142493. volume
  142494. volumes
  142495. kowarsch
  142496. heteropentalenes
  142497. heterocyclic
  142498. ferrocen
  142499. sonntag
  142500. radical
  142501. reactions
  142502. carbohydrates
  142503. sonntag
  142504. clemens
  142505. schuchmann
  142506. heinz
  142507. peter
  142508. elucidation
  142509. vonoids
  142510. vorbrueggen
  142511. vorbruggen
  142512. voronenkov
  142513. voronkov
  142514. voronkov
  142515. chernov
  142516. mixed
  142517. organic
  142518. derivatives
  142519. mercur
  142520. voronkov
  142521. deryagina
  142522. thermal
  142523. reactions
  142524. thiyl
  142525. radica
  142526. voronkov
  142527. maletina
  142528. roman
  142529. heterosiloxanes
  142530. voronkow
  142531. voronkow
  142532. biological
  142533. activity
  142534. silatranes
  142535. voronov
  142536. voropaeva
  142537. vorspohl
  142538. voskanyan
  142539. vostrikova
  142540. samarai
  142541. functionalized
  142542. carbodiimides
  142543. vrieze
  142544. vroom
  142545. vuilleumier
  142546. vulcanization
  142547. vuorinen
  142548. vurov
  142549. vvedenskii
  142550. vyazankin
  142551. vygodskii
  142552. vyplel
  142553. vyshinskaya
  142554. vyunov
  142555. vyunov
  142556. ginak
  142557. mechanism
  142558. electrophilic
  142559. browne
  142560. ladybug
  142561. alkaloids
  142562. including
  142563. szabo
  142564. chlorosulfonyl
  142565. isocyanate
  142566. aldrichimica
  142567. chemistry
  142568. dioxetanes
  142569. advances
  142570. alkenyl
  142571. nitroalkyl
  142572. radicals
  142573. radical
  142574. chain
  142575. reactions
  142576. ylide
  142577. formation
  142578. rearrangement
  142579. reaction
  142580. munslow
  142581. delia
  142582. syntheses
  142583. dmowski
  142584. fluor
  142585. advances
  142586. fluorination
  142587. dopke
  142588. lactonalkaloide
  142589. amaryllidaceen
  142590. hetero
  142591. durckheimer
  142592. anqew
  142593. tetracyclines
  142594. durckheimer
  142595. blumbach
  142596. lattrell
  142597. scheunemann
  142598. truce
  142599. klinger
  142600. brand
  142601. sulfones
  142602. sulfoximine
  142603. flitsch
  142604. schindler
  142605. synthesis
  142606. alkenylation
  142607. kunau
  142608. angew
  142609. chemistry
  142610. biochem
  142611. hehre
  142612. topsom
  142613. initio
  142614. calculations
  142615. kantlehner
  142616. funke
  142617. kienitz
  142618. maier
  142619. kirmse
  142620. angew
  142621. nitrogen
  142622. leaving
  142623. klopffer
  142624. intramolecular
  142625. proton
  142626. transfer
  142627. electronically
  142628. kutzelnigg
  142629. quantum
  142630. chemical
  142631. studies
  142632. related
  142633. weeks
  142634. rohrer
  142635. crystal
  142636. structures
  142637. armarego
  142638. stereochemistry
  142639. heterocyclic
  142640. compounds
  142641. cheletropic
  142642. reactions
  142643. pericyclic
  142644. reactions
  142645. sachtler
  142646. sanien
  142647. surface
  142648. composition
  142649. jones
  142650. brinker
  142651. pericyclic
  142652. reactions
  142653. carbe
  142654. jones
  142655. carbene
  142656. carbene
  142657. rearrangements
  142658. solution
  142659. speckamp
  142660. hiemstra
  142661. tetrahedron
  142662. intramo
  142663. oppolzer
  142664. intramolecular
  142665. cycloadditions
  142666. oppolzer
  142667. tetrahedron
  142668. synthetic
  142669. applications
  142670. jencks
  142671. gilbert
  142672. general
  142673. catalysis
  142674. weber
  142675. gokel
  142676. phase
  142677. transfer
  142678. catalysis
  142679. organic
  142680. mckean
  142681. biochemistry
  142682. steroids
  142683. other
  142684. johnson
  142685. angew
  142686. biomimetic
  142687. polyene
  142688. sliwa
  142689. thomas
  142690. heterocycles
  142691. chemistry
  142692. sliwa
  142693. matusiak
  142694. postawka
  142695. heterocycles
  142696. steglich
  142697. jeschke
  142698. buschmann
  142699. tagaki
  142700. sulfides
  142701. organic
  142702. chemistry
  142703. sulfur
  142704. plenu
  142705. dower
  142706. vollhardt
  142707. tetrahedron
  142708. therm
  142709. verboom
  142710. reinhoudt
  142711. recent
  142712. wehrli
  142713. ansamycins
  142714. chemistry
  142715. biosynthesis
  142716. activity
  142717. w-dienes
  142718. wachter
  142719. wacker
  142720. wadepohl
  142721. wadepohl
  142722. hubert
  142723. benzene
  142724. derivatives
  142725. bridging
  142726. wadsworth
  142727. wadsworth
  142728. synthetic
  142729. applications
  142730. phosphoryl
  142731. stabil
  142732. wadsworth-emmons
  142733. orth-emmons
  142734. reaction
  142735. revisite
  142736. waegall
  142737. waegell
  142738. wagenknecht
  142739. waghela
  142740. wagle
  142741. wagner
  142742. wagner
  142743. jauregg
  142744. thermal
  142745. photochemical
  142746. addition
  142747. dieno
  142748. wagner
  142749. jauregg
  142750. thermal
  142751. photochemical
  142752. additions
  142753. wagner
  142754. findeisen
  142755. schafer
  142756. dietrich
  142757. diisocyanatoca
  142758. wagner
  142759. photorearrangements
  142760. biradicals
  142761. simple
  142762. wagner
  142763. peter
  142764. photoinduced
  142765. hydrogen
  142766. wagner-meerwein
  142767. wagner-meerwein
  142768. rearrangements
  142769. wahba
  142770. wahlberg
  142771. wahlberg
  142772. eklund
  142773. cembranoids
  142774. pseudopteranoids
  142775. cubit
  142776. wahlberg
  142777. eklund
  142778. cyclized
  142779. cembranoids
  142780. natural
  142781. occurr
  142782. waichiro
  142783. waigh
  142784. wakabayashi
  142785. wakefield
  142786. wakefield
  142787. wright
  142788. isoxazole
  142789. chemistry
  142790. since
  142791. wakeham
  142792. wakselman
  142793. wakselman
  142794. claude
  142795. single
  142796. electron
  142797. transfer
  142798. processes
  142799. perfl
  142800. walborsky
  142801. walborsky
  142802. cyclopropyl
  142803. radical
  142804. tetrahedr
  142805. waldeck
  142806. waldeck
  142807. david
  142808. photoisomerization
  142809. dynamics
  142810. stilbenes
  142811. waldemar
  142812. waldmannw
  142813. waldmann
  142814. asymmetric
  142815. hetero
  142816. diels
  142817. alder
  142818. reactions
  142819. synthesisw
  142820. waldmann
  142821. herbert
  142822. braun
  142823. matthias
  142824. amino
  142825. esters
  142826. chiral
  142827. waldmann
  142828. herbert
  142829. licio4
  142830. ether
  142831. unusual
  142832. solvent
  142833. angew
  142834. waldmann
  142835. herbert
  142836. sebastian
  142837. dagmar
  142838. enzymic
  142839. protecting
  142840. group
  142841. walenta
  142842. rearrangements
  142843. bicyclic
  142844. compounds
  142845. walker
  142846. walker
  142847. andrew
  142848. asymmetric
  142849. carbon
  142850. carbon
  142851. formation
  142852. walker
  142853. transformations
  142854. phosphorus
  142855. stabilized
  142856. anions
  142857. wallace
  142858. wallace
  142859. hydroxylamine
  142860. sulfonic
  142861. versatile
  142862. synthe
  142863. wallbaum
  142864. wallbaum
  142865. sabine
  142866. martens
  142867. jurgen
  142868. asymmetric
  142869. syntheses
  142870. walling
  142871. walling
  142872. cheves
  142873. fifty
  142874. years
  142875. radicals
  142876. profiles
  142877. pathway
  142878. walling
  142879. cheves
  142880. nature
  142881. radicals
  142882. involved
  142883. grignard
  142884. wallington
  142885. wallington
  142886. dagaut
  142887. kurylo
  142888. absorption
  142889. cross
  142890. secti
  142891. wallis
  142892. walls
  142893. walsh
  142894. walsh
  142895. synthesis
  142896. aminobenzophenones
  142897. walter
  142898. walters
  142899. walton
  142900. walton
  142901. bridgehead
  142902. radicals
  142903. 199221
  142904. chemical
  142905. walton
  142906. bridgehead
  142907. radicals
  142908. chemical
  142909. society
  142910. reviews
  142911. theory
  142912. applications
  142913. chemically
  142914. induced
  142915. peter
  142916. shukla
  142917. deepak
  142918. utility
  142919. behavior
  142920. wanda
  142921. wander
  142922. wandering
  142923. wandless
  142924. wands
  142925. bradshaw
  142926. izatt
  142927. applications
  142928. spectral
  142929. wangnic
  142930. wannagat
  142931. warcup
  142932. david
  142933. peptide
  142934. pharmaceuticals
  142935. approaches
  142936. lignans
  142937. neolignans
  142938. related
  142939. compounds
  142940. natural
  142941. synthesis
  142942. podophyllotoxin
  142943. related
  142944. compounds
  142945. robert
  142946. bifunctional
  142947. compounds
  142948. oxford
  142949. chemistry
  142950. primer
  142951. waring
  142952. warman
  142953. warman
  142954. jonker
  142955. stephan
  142956. schuddeboom
  142957. wouter
  142958. warner
  142959. warnhoff
  142960. warren
  142961. warren
  142962. phosphorus
  142963. sulphur
  142964. reagents
  142965. synthesis
  142966. warren
  142967. reagents
  142968. natural
  142969. product
  142970. synthesis
  142971. based
  142972. warsaw
  142973. warsz
  142974. warwel
  142975. warwel
  142976. siegfried
  142977. sojka
  142978. michael
  142979. rusch
  142980. klaas
  142981. synthesi
  142982. washburne
  142983. washington
  142984. wasielewski
  142985. wasps
  142986. wasserman
  142987. wasserman
  142988. singlet
  142989. oxygen
  142990. organic
  142991. synthesis
  142992. wasserman
  142993. lipshutz
  142994. reactions
  142995. singlet
  142996. oxygen
  142997. waste
  142998. watanabe
  142999. wataru
  143000. watch
  143001. wateru
  143002. organic
  143003. reactions
  143004. water-promoted
  143005. water-promoted
  143006. organic-reactions
  143007. water-soluble
  143008. water-soluble
  143009. ligands
  143010. metal
  143011. complexes
  143012. complex
  143013. catalysts
  143014. water-tolerant
  143015. watsonn
  143016. watson
  143017. watthey
  143018. watts
  143019. wavelength
  143020. waves
  143021. waxman
  143022. waymouth
  143023. wayne
  143024. wayner
  143025. wayner
  143026. danial
  143027. parker
  143028. vernon
  143029. energies
  143030. solution
  143031. weakly
  143032. geoffrey
  143033. winfield
  143034. routes
  143035. alternative
  143036. haloca
  143037. thomas
  143038. wilcox
  143039. craig
  143040. enantioselective
  143041. anddiastereose
  143042. webber
  143043. weber
  143044. weber
  143045. vogtle
  143046. crown
  143047. compounds
  143048. introductory
  143049. overvi
  143050. weber
  143051. homoleptic
  143052. noble
  143053. metal
  143054. carbonyl
  143055. cations
  143056. angew
  143057. weber
  143058. gokel
  143059. phase
  143060. transfer
  143061. catalysis
  143062. applications
  143063. webster
  143064. weedon
  143065. weeks
  143066. weghorn
  143067. wehinger
  143068. wehrli
  143069. wehrli
  143070. nishida
  143071. natural
  143072. products
  143073. weidmann
  143074. weight
  143075. weill
  143076. weinheim
  143077. weinheimer
  143078. weinheimer
  143079. chang
  143080. matson
  143081. naturally
  143082. occurring
  143083. weinreb
  143084. weinreb
  143085. levin
  143086. synthesis
  143087. nitrogen
  143088. containing
  143089. heter
  143090. weinstein
  143091. weirich
  143092. weishan
  143093. weisman
  143094. weiss
  143095. weiss
  143096. norrish
  143097. reaction
  143098. cycloalkanone
  143099. photo
  143100. weiss
  143101. edwards
  143102. biosynthesis
  143103. aromatic
  143104. compounds
  143105. weissberger
  143106. weissermel
  143107. weissermel
  143108. klaus
  143109. jurgen
  143110. industrial
  143111. organic
  143112. chemist
  143113. weisshaar
  143114. weisshaar
  143115. james
  143116. transition
  143117. metal
  143118. atoms
  143119. weitz
  143120. weiyuan
  143121. weizmann
  143122. welch
  143123. weldon
  143124. welker
  143125. welker
  143126. cycloaddition
  143127. reactions
  143128. transition
  143129. wells
  143130. welter
  143131. weltner
  143132. wenchen
  143133. wender
  143134. wender
  143135. cribbs
  143136. cynthia
  143137. computer
  143138. assisted
  143139. molecular
  143140. wendt
  143141. wendy
  143142. wenger
  143143. wenieb
  143144. wenjie
  143145. wenkert
  143146. wenkert
  143147. oxycyclopropanes
  143148. organochemical
  143149. synthesis
  143150. wenqi
  143151. wentrup
  143152. wentrup
  143153. carbenes
  143154. nitrenes
  143155. heterocyclic
  143156. chemistry
  143157. wentrup
  143158. behavior
  143159. arylcarbenes
  143160. nitrenes
  143161. wentrup
  143162. kambouns
  143163. peter
  143164. sulfides
  143165. dinitrogen
  143166. sulfide
  143167. wentworth
  143168. gerhard
  143169. cyclodextrins
  143170. building
  143171. blocks
  143172. supramolec
  143173. werner
  143174. weisshaar@
  143175. werner
  143176. what's@
  143177. which
  143178. widmer@
  143179. wiley
  143180. william
  143181. williams
  143182. robert
  143183. early
  143184. carboranes
  143185. their
  143186. structural
  143187. lega@
  143188. winterfeldt@
  143189. withanolides@
  143190. fgang
  143191. carbon
  143192. carbon
  143193. coupling
  143194. constants
  143195. compilation
  143196. thebtaranonth
  143197. synthesis
  143198. yakobson
  143199. furin
  143200. antimony
  143201. pentahalides
  143202. catalysis
  143203. yamamoto
  143204. yoshinori
  143205. shida
  143206. naomi
  143207. stereochemistry
  143208. mechanism
  143209. yasuhiro@
  143210. ylide
  143211. ylides
  143212. stabilized
  143213. fluoro
  143214. perfluoroalkyl
  143215. sulfonyl
  143216. groups@
  143217. younes
  143218. mansour
  143219. ismail
  143220. hussein
  143221. metwally
  143222. saoud
  143223. gevaza
  143224. staninets
  143225. heterocycl
  143226. compounds
  143227. zahir@
  143228. zassinovich
  143229. grazia
  143230. mestroni
  143231. giovanni
  143232. gladiali
  143233. serafino
  143234. asymm@
  143235. zemskov
  143236. zhubanov@
  143237. werner
  143238. werner
  143239. novel
  143240. types
  143241. metal
  143242. metal
  143243. bonded
  143244. complexes
  143245. contain
  143246. werner-type
  143247. werstiuk
  143248. wessjohann
  143249. barton
  143250. organosilicon
  143251. chemistry
  143252. parts
  143253. chemistry
  143254. oxocarbons
  143255. israel
  143256. journa
  143257. history
  143258. oxocarbons
  143259. oxocarbons
  143260. academic
  143261. westerhoff
  143262. westheimer
  143263. westheimer
  143264. monomeric
  143265. metaphosphates
  143266. chemical
  143267. westheimer
  143268. polytopal
  143269. rearrangement
  143270. phosphorus
  143271. westiellamide
  143272. westley
  143273. westmoreland
  143274. weston
  143275. westwood
  143276. wet-alumina
  143277. wetter
  143278. wetzel
  143279. whaley
  143280. whangbo
  143281. wheller
  143282. where
  143283. whetten
  143284. which
  143285. which
  143286. which
  143287. factors
  143288. determine
  143289. reactivity
  143290. regioselectivity
  143291. whisky
  143292. whistler
  143293. whitall
  143294. white
  143295. white
  143296. david
  143297. coville
  143298. quantification
  143299. steric
  143300. effects
  143301. whitesell
  143302. whitesell
  143303. james
  143304. cyclohexyl
  143305. based
  143306. chiral
  143307. auxiliaries
  143308. whitesides
  143309. whitesides
  143310. george
  143311. mathias
  143312. christopher
  143313. molecu
  143314. whiting
  143315. whittaker
  143316. whitten
  143317. whitten
  143318. photochemical
  143319. reactions
  143320. surfactant
  143321. molecules
  143322. whitten
  143323. photochemistry
  143324. porphyrins
  143325. their
  143326. metal
  143327. whitten
  143328. photoinduced
  143329. electron
  143330. transfer
  143331. reactions
  143332. whittlesey
  143333. whitton
  143334. whizz
  143335. whole
  143336. wiberg
  143337. wiberley
  143338. wicha
  143339. widdig
  143340. widdowson
  143341. widing
  143342. widmer
  143343. widmer
  143344. synthetic
  143345. advances
  143346. wieczorek
  143347. wiegand
  143348. wiegand
  143349. benjamin
  143350. friend
  143351. cynthia
  143352. model
  143353. studies
  143354. wiejak
  143355. wieland
  143356. wieland
  143357. bodanszky
  143358. world
  143359. peptides
  143360. brief
  143361. history
  143362. wieland-gumlich
  143363. wielstra
  143364. wierenga
  143365. wierenga
  143366. total
  143367. synthesis
  143368. ionophores
  143369. total
  143370. wierlacher
  143371. wiersum
  143372. wiersum
  143373. isobenzofuran
  143374. related
  143375. quinonoid
  143376. systems
  143377. wierzchleyski
  143378. wieslaw
  143379. wiesner
  143380. wiesner
  143381. strategy
  143382. synthesis
  143383. polycyclic
  143384. polysubsti
  143385. wigfield
  143386. wigfield
  143387. stereochemistry
  143388. mechanism
  143389. ketone
  143390. reducti
  143391. wiiliam
  143392. wijesekera
  143393. wijesekera
  143394. tilak
  143395. dolphin
  143396. david
  143397. bromo
  143398. methylbiladienes
  143399. wijnand
  143400. wijnberg
  143401. wilberth
  143402. wilby
  143403. wilcox
  143404. wilds
  143405. wilen
  143406. wileyL
  143407. wiley
  143408. wiley
  143409. wilfred
  143410. wilfried
  143411. wilhelm
  143412. wiliam
  143413. wilkinson
  143414. wilkinson
  143415. recent
  143416. advances
  143417. selective
  143418. formation
  143419. willem
  143420. willemse
  143421. willen
  143422. willett
  143423. willgerodt
  143424. willi
  143425. william
  143426. william
  143427. williams
  143428. williams
  143429. ibrahim
  143430. carbodiimide
  143431. chemistry
  143432. recent
  143433. advance
  143434. williams
  143435. diagnosis
  143436. concerted
  143437. organic
  143438. mechanisms
  143439. williams
  143440. andrew
  143441. effective
  143442. charge
  143443. transition
  143444. state
  143445. struct
  143446. williams
  143447. charles
  143448. harpp
  143449. david
  143450. sulfur
  143451. extrusion
  143452. reactions
  143453. williams
  143454. buncel
  143455. aromatic
  143456. cationic
  143457. reactions
  143458. isotopes
  143459. williams
  143460. dudley
  143461. molecular
  143462. basis
  143463. biological
  143464. order
  143465. williams
  143466. interplay
  143467. theory
  143468. experiment
  143469. williams
  143470. electrical
  143471. conduction
  143472. organic
  143473. solids
  143474. williams
  143475. richard
  143476. kurtz
  143477. henry
  143478. homoaromaticity
  143479. advances
  143480. williams
  143481. robert
  143482. early
  143483. carboranes
  143484. their
  143485. structural
  143486. williams
  143487. robert
  143488. polyborane
  143489. carborane
  143490. carbocation
  143491. conti
  143492. williams
  143493. robert
  143494. asymmetric
  143495. syntheses
  143496. alpha
  143497. amino
  143498. acids
  143499. williams
  143500. robert
  143501. hendrix
  143502. james
  143503. asymmetric
  143504. synthesis
  143505. williams
  143506. robert
  143507. robinson
  143508. chemist
  143509. extraordinary
  143510. clarendon
  143511. williamson
  143512. willima
  143513. willis
  143514. willner
  143515. wills_
  143516. wills
  143517. polycarbocyclic
  143518. compounds
  143519. separate
  143520. systems_
  143521. wills
  143522. studley
  143523. asymmetric
  143524. reduction
  143525. ketones
  143526. willy
  143527. wilman
  143528. wilson
  143529. wilson
  143530. marshall
  143531. schnapp
  143532. karlyn
  143533. intensity
  143534. laser
  143535. wilson
  143536. stephen
  143537. anion
  143538. assisted
  143539. sigmatropic
  143540. rearrangements
  143541. wimmele
  143542. wimmer
  143543. winans
  143544. winfield
  143545. wingender
  143546. winiarski
  143547. winnik
  143548. winnik
  143549. cyclization
  143550. conformation
  143551. hydrocarbon
  143552. winstein-holness
  143553. winter
  143554. winterfeldt
  143555. winterfeldt
  143556. ekkehard
  143557. directedstereoselect
  143558. alkaloid
  143559. synthe
  143560. winterfeldt
  143561. ekkehard
  143562. enantiomerically
  143563. cyclopentadienes
  143564. winters
  143565. wintgens
  143566. wintner
  143567. wintner
  143568. edward
  143569. morgan
  143570. rebek
  143571. julius
  143572. studies
  143573. wipke
  143574. wiseman
  143575. wiseman
  143576. introduction
  143577. industrial
  143578. organic
  143579. chemistry
  143580. wiswesser
  143581. witczak
  143582. witczak
  143583. synthesis
  143584. glycosyl
  143585. compounds
  143586. other
  143587. with_
  143588. witkop
  143589. wittenberger
  143590. wittenberger
  143591. recent
  143592. developments
  143593. tetrazole
  143594. chemistry
  143595. wittig
  143596. wittig
  143597. fination
  143598. reaction
  143599. carbonyl
  143600. compounds
  143601. other
  143602. wittig-horner
  143603. witulski
  143604. wladislaw
  143605. wladislaw
  143606. blanka
  143607. marzorati
  143608. liliana
  143609. reactions
  143610. sulfinyl
  143611. wladyslaw
  143612. wlodzimierz
  143613. wlodzmmierz
  143614. stanislaw
  143615. sulfur
  143616. seleno
  143617. sugar
  143618. modified
  143619. nucleoside
  143620. woggon
  143621. woggon
  143622. dietrich
  143623. fretz
  143624. heinz
  143625. mechanism
  143626. cytochrome
  143627. woiff
  143628. wojcicki
  143629. wojcicki
  143630. andrew
  143631. mononuclear
  143632. transition
  143633. metal
  143634. propargyl/a
  143635. wojciech
  143636. wolber
  143637. wolfe
  143638. wolfe
  143639. ogliaruso
  143640. synthesis
  143641. carboxylic
  143642. acids
  143643. esters
  143644. wolff
  143645. wolff-kishner
  143646. wolfgang
  143647. wolfgang
  143648. wolfram
  143649. wolken
  143650. wolter
  143651. wolters
  143652. wongi
  143653. kevin
  143654. kajimoto
  143655. tetsuya
  143656. lihren
  143657. whitesides
  143658. george
  143659. enzymes
  143660. synthetic
  143661. organ
  143662. cyclopropanes
  143663. second
  143664. supplements
  143665. woodgate
  143666. woodward
  143667. words
  143668. works
  143669. world
  143670. wortmann
  143671. wortmann
  143672. ruediger
  143673. schmittgen
  143674. detzer
  143675. norbert
  143676. photoinduce
  143677. wotter
  143678. wouter
  143679. wovkulich
  143680. wozniak
  143681. wozniak
  143682. marian
  143683. amination
  143684. nitroazaarom
  143685. wrackmeyer
  143686. wrackmeyer
  143687. carbon
  143688. spectroscopy
  143689. boron
  143690. compounds
  143691. carbon
  143692. carbon
  143693. coupling
  143694. constants
  143695. compilation
  143696. wright
  143697. wright
  143698. axelson
  143699. physical
  143700. chemical
  143701. applicatio
  143702. wright
  143703. orthosomycins
  143704. family
  143705. antibiotics
  143706. wrighton
  143707. writing
  143708. wrobel
  143709. wubbels
  143710. wubbles
  143711. wucherer
  143712. chemical
  143713. properties
  143714. buckminsterfullerene
  143715. wuest
  143716. wulff
  143717. wulfman
  143718. wulfman
  143719. poling
  143720. metal
  143721. catalyzed
  143722. carbenoids
  143723. reactiv
  143724. wurmbaeoideae
  143725. wydawn
  143726. wyman
  143727. wynberg
  143728. wynberg
  143729. chance
  143730. necessity
  143731. asymmetric
  143732. catalysis
  143733. wysocki
  143734. systems
  143735. potential
  143736. dipoles
  143737. decarboxylative
  143738. x-14547a
  143739. x-double
  143740. x-ray
  143741. x-ray
  143742. structural
  143743. analyses
  143744. organomagnesium
  143745. compounds
  143746. x-ray
  143747. structural
  143748. analysis
  143749. organolithium
  143750. compounds
  143751. xanes
  143752. xanthate
  143753. xanthate
  143754. transfer
  143755. addition
  143756. glycine
  143757. radical
  143758. equivalent
  143759. xanthates
  143760. xanthine
  143761. xanthones
  143762. xanthonoids
  143763. xanthylium
  143764. xanthylium
  143765. salts
  143766. dibenzo
  143767. pyrylium
  143768. salts
  143769. xavier
  143770. xenobiotics
  143771. xenon
  143772. xenon
  143773. difluoride
  143774. fluorinating
  143775. agents
  143776. organic
  143777. synthesi
  143778. xestoquinone
  143779. xestospongin
  143780. xiang
  143781. xiangfu
  143782. xiaofeng
  143783. xiaoping
  143784. xiaoyong
  143785. xidation
  143786. xidation
  143787. nitrogen
  143788. phosphorus
  143789. xidative
  143790. xidative
  143791. coupling
  143792. phenols
  143793. phenol
  143794. ethers
  143795. fluorospectrochemist
  143796. within
  143797. cyclodex
  143798. pseudomonas
  143799. fluorescens
  143800. lipase
  143801. asymmetric
  143802. xihai
  143803. xikui
  143804. xiyan
  143805. zhifu
  143806. benjamin
  143807. moore
  143808. jeffrey
  143809. stiff
  143810. dendritic
  143811. macro
  143812. xuegong
  143813. xylolactone
  143814. xylose
  143815. xylylenes
  143816. asakawa
  143817. takemoto
  143818. sesquiterpene
  143819. lactones
  143820. heterocy
  143821. freimanis
  143822. kikovskaya
  143823. heterocycl
  143824. compounds
  143825. inubushi
  143826. ibuak
  143827. synthesis
  143828. pumiliotoxin
  143829. toxic
  143830. izumi
  143831. stereo
  143832. differentiating
  143833. reactions
  143834. natur
  143835. kishi
  143836. synthetic
  143837. studies
  143838. kurasawa
  143839. takada
  143840. heterocycles
  143841. recent
  143842. mazur
  143843. functionalization
  143844. recent
  143845. advances
  143846. chemistr
  143847. shimizu
  143848. dinoflagellate
  143849. toxins
  143850. marine
  143851. natural
  143852. products
  143853. takeuchi
  143854. furusaki
  143855. chemistry
  143856. isoxazolidines
  143857. tamura
  143858. minamikawa
  143859. ikeda
  143860. mesitylenesulfonylhy
  143861. thebtaranonth
  143862. synthesis
  143863. international
  143864. symposium
  143865. yamamoto
  143866. anqew
  143867. selective
  143868. yablokov
  143869. yablokov
  143870. mechanisms
  143871. rearrangements
  143872. peroxid
  143873. yablokova
  143874. yadav
  143875. yagupol'skii
  143876. yagupolskii
  143877. yagupolsky
  143878. yagupolsky
  143879. ylides
  143880. stabilized
  143881. fluoro
  143882. perfluoroalkyl
  143883. yahioglu
  143884. yajima
  143885. yakhimovich
  143886. yakhimovich
  143887. synthesis
  143888. active
  143889. metabolites
  143890. yakhontov
  143891. yakhontov
  143892. recent
  143893. advances
  143894. quinuclidine
  143895. chemistry
  143896. yakhot
  143897. yakhot
  143898. what's
  143899. excimers
  143900. 197811
  143901. advances
  143902. yakirevitch
  143903. yakobson
  143904. yakobson
  143905. furin
  143906. antimony
  143907. pentahalides
  143908. catalysis
  143909. yakugaku
  143910. yakugaku
  143911. zasshi
  143912. pharm
  143913. studies
  143914. total
  143915. yalkowsky
  143916. yalkowsky
  143917. samuel
  143918. banerjee
  143919. sujit
  143920. aqueous
  143921. solubility
  143922. methods
  143923. yalpani
  143924. yamabe
  143925. yamada
  143926. yamada
  143927. yamamoto
  143928. yoshinori
  143929. development
  143930. reacti
  143931. yamaguchi
  143932. yamakawa
  143933. yamamoto
  143934. yamamoto
  143935. carbon
  143936. oxygen
  143937. activation
  143938. transition
  143939. yamamoto
  143940. nozaki
  143941. selective
  143942. reactions
  143943. organoaluminum
  143944. yamamoto
  143945. extended
  143946. systems
  143947. closed
  143948. helicene
  143949. synthesis
  143950. yamamoto
  143951. yoshinori
  143952. entry
  143953. carbanion
  143954. chemistry
  143955. yamamoto
  143956. yoshinori
  143957. naoki
  143958. selective
  143959. reactions
  143960. using
  143961. yamamoto
  143962. yoshinori
  143963. molecular
  143964. design
  143965. synthesis
  143966. boron
  143967. yamamoto
  143968. yoshinori
  143969. shida
  143970. naomi
  143971. stereochemistry
  143972. mechanism
  143973. yamamoto
  143974. yoshinori
  143975. shida
  143976. naomi
  143977. stereochemistry
  143978. mechanism
  143979. yamamura
  143980. yamanaka
  143981. yamanaka
  143982. hiroshi
  143983. contributions
  143984. professor
  143985. masatomo
  143986. hamana
  143987. yamano
  143988. yamashita
  143989. yamazaki
  143990. yamazaki
  143991. benedetti
  143992. goodman
  143993. conformational
  143994. requi
  143995. yamazaki
  143996. kawai
  143997. hydrogenolytic
  143998. behavior
  143999. asymmetric
  144000. yambushev
  144001. yambushev
  144002. savin
  144003. stereochemistry
  144004. organoarsenic
  144005. yamskov
  144006. yanada
  144007. yanada
  144008. reiko
  144009. harayama
  144010. takashi
  144011. yoneda
  144012. fumio
  144013. chemistry
  144014. yandewalle
  144015. yandovskii
  144016. yandovskii
  144017. gidaspov
  144018. tselinskii
  144019. formation
  144020. yandovskii
  144021. gidaspov
  144022. tselinskii
  144023. formation
  144024. yannick
  144025. yannoni
  144026. yanovskaya
  144027. yaozeng
  144028. yasar
  144029. yashin
  144030. yashina
  144031. yashina
  144032. vereshchagin
  144033. natural
  144034. synthetic
  144035. acetyleni
  144036. yashwamt
  144037. yasuda
  144038. yasufumi
  144039. yasuhiro
  144040. yasumasa
  144041. yasuo
  144042. yasutaka
  144043. yasutake
  144044. yates
  144045. yates
  144046. huckel
  144047. molecular
  144048. orbital
  144049. theory
  144050. academic
  144051. press
  144052. ycles
  144053. ycloadditions
  144054. mckervey
  144055. anthony
  144056. organic
  144057. synthesis
  144058. diazo
  144059. yeajer
  144060. yearm
  144061. years
  144062. yeast
  144063. yicens
  144064. yield
  144065. yielding
  144066. yields
  144067. yingtai
  144068. yingzhaosu
  144069. ylamines
  144070. ylate
  144071. ylcarboxylate
  144072. ylide
  144073. ylide
  144074. ylide
  144075. formation
  144076. rearrangement
  144077. reaction
  144078. carbene
  144079. ylide
  144080. formation
  144081. rearrangemment
  144082. reaction
  144083. carben
  144084. ylide
  144085. formation
  144086. reaction
  144087. carbenes
  144088. carbenoids
  144089. ylide-alkene
  144090. ylide-forming
  144091. ylidene
  144092. ylidenebutenolides
  144093. ylidenemalonodinitri
  144094. ylidenemalononitrile
  144095. ylidenetetronic
  144096. ylides
  144097. ylides
  144098. imines
  144099. phosphorus
  144100. ylides
  144101. desilyl
  144102. alpha-silyl
  144103. onium
  144104. salts
  144105. ylides
  144106. stabilized
  144107. fluoro
  144108. perfluoroalkyl
  144109. sulfonyl
  144110. groups
  144111. ylids
  144112. ylmethyl
  144113. yltellurium
  144114. ylthio
  144115. yltributylstannane
  144116. ymers
  144117. ymmetric
  144118. ynals
  144119. ynamine
  144120. ynamine
  144121. versatile
  144122. organic
  144123. synthesis
  144124. ynamines
  144125. ynols
  144126. ynones
  144127. ynthesis
  144128. ynthons
  144129. yoakim
  144130. yohei
  144131. yohimane
  144132. yohimban
  144133. yohimbine
  144134. yohimboid
  144135. yohimbone
  144136. yokomatsu
  144137. yokomatsu
  144138. tsutomu
  144139. yuasa
  144140. shibuya
  144141. shiroshi
  144142. synthesis
  144143. yokota
  144144. yokoyama
  144145. yolande
  144146. yonashiro
  144147. yoneda
  144148. yoneda
  144149. norihiko
  144150. combination
  144151. hydrogen
  144152. fluoride
  144153. yonemitsu
  144154. mariano
  144155. patrick
  144156. mechanistic
  144157. synthetic
  144158. yoram
  144159. yorkO
  144160. yoshi
  144161. yoshida
  144162. yoshida
  144163. murata
  144164. toshiki
  144165. matsunaga
  144166. shinichiro
  144167. maekawa
  144168. yoshida
  144169. masato
  144170. kamigata
  144171. nobumasa
  144172. recent
  144173. progress
  144174. perfluor
  144175. yoshida
  144176. masato
  144177. utility
  144178. highly
  144179. electrophilic
  144180. peroxides
  144181. yoshida
  144182. takashi
  144183. hatano
  144184. tsutomu
  144185. kuwajima
  144186. takako
  144187. okuda
  144188. takuo
  144189. yoshifuji
  144190. yoshifumi
  144191. yoshihide
  144192. yoshihiko
  144193. yoshihisa
  144194. yoshikawa
  144195. yoshiki
  144196. yoshikoshi
  144197. yoshimitsu
  144198. yoshimura
  144199. yoshino
  144200. yoshinori
  144201. yoshinosuke
  144202. yoshio
  144203. yoshioka
  144204. yoshiro
  144205. yoshito
  144206. yoshitsugu
  144207. yoshiya
  144208. youhua
  144209. younes
  144210. younes
  144211. mansour
  144212. ismail
  144213. hussein
  144214. metwally
  144215. saoud
  144216. young
  144217. young
  144218. douglas
  144219. stereochemistry
  144220. metabolic
  144221. reactions
  144222. young
  144223. spectroscopy
  144224. carbanions
  144225. carbocations
  144226. yousaf
  144227. yousef
  144228. yoyori
  144229. yoyori
  144230. organic
  144231. synthesis
  144232. polybromo
  144233. ketone
  144234. yrimidine
  144235. yrylium
  144236. ysahunskii
  144237. ysahunskii
  144238. kholodov
  144239. chemistry
  144240. sydnone
  144241. imines
  144242. ytterbium
  144243. gevaza
  144244. staninets
  144245. heterocycl
  144246. compds
  144247. gevaza
  144248. staninets
  144249. heterocycl
  144250. compounds
  144251. mitin
  144252. zapelevova
  144253. methods
  144254. peptide
  144255. synthesis
  144256. yuasa
  144257. yudevich
  144258. yudevich
  144259. sokolov
  144260. ionin
  144261. phosphinates
  144262. hypophosphit
  144263. yufit
  144264. yuichi
  144265. yukishige
  144266. yukito
  144267. yunusov
  144268. yunusov
  144269. diterpenoid
  144270. alkaloids
  144271. natural
  144272. product
  144273. reports
  144274. yur'eva
  144275. yuriy
  144276. yurtanov
  144277. yusaku
  144278. yusuke
  144279. yutaka
  144280. yuvenskii
  144281. yuxiang
  144282. yuxiang
  144283. boren
  144284. jiarong
  144285. shuan
  144286. jianjun
  144287. huiping
  144288. yuzuriha
  144289. yuzuru
  144290. yvonne
  144291. yysen
  144292. alkylidene
  144293. dihydro
  144294. hydroxy
  144295. methyl
  144296. furanones
  144297. reactions
  144298. alpha
  144299. heterocarbanions
  144300. synthesis
  144301. properties
  144302. triazo
  144303. diisopropyllidene-a
  144304. allyl
  144305. tributylstannane
  144306. rappoport
  144307. mechanistic
  144308. selective
  144309. synthesis
  144310. homoallylic
  144311. alcohols
  144312. alkenyla
  144313. todres
  144314. tetrahedron
  144315. radical
  144316. organic
  144317. zvonkova
  144318. structural
  144319. chemistry
  144320. substituted
  144321. benzenes
  144322. zabirov
  144323. zabirov
  144324. shamsevaleev
  144325. cherkasov
  144326. phosphorylated
  144327. zablocka
  144328. zabolotskii
  144329. zabotina
  144330. zabusova
  144331. zachariasse
  144332. zachariasse
  144333. klaas
  144334. thomas
  144335. hebecker
  144336. leinho
  144337. zahia
  144338. zahir
  144339. zahner
  144340. zahradnik
  144341. zaichenko
  144342. zaikin
  144343. zaikov
  144344. zainullin
  144345. zajdel
  144346. zakharkin
  144347. zakharkin
  144348. guseva
  144349. chemistry
  144350. cyclododecatri
  144351. zaklika
  144352. zakrewski
  144353. zalewsli
  144354. zalewsli
  144355. romuald
  144356. krygowski
  144357. tadeusz
  144358. shorter
  144359. zaman
  144360. zaman
  144361. sharma
  144362. aspects
  144363. chemistry
  144364. zamaraev
  144365. zamaraev
  144366. khairutdinov
  144367. photoinduced
  144368. electron
  144369. tunnelin
  144370. zamarlik
  144371. zamecka
  144372. zamir
  144373. zamoiski
  144374. zander
  144375. zanello
  144376. zanello
  144377. piero
  144378. chains
  144379. clusters
  144380. inclusion
  144381. compounds
  144382. paramag
  144383. zangrando
  144384. zanirato
  144385. zaoral
  144386. zapelevova
  144387. zappala
  144388. zaragoza
  144389. zaragozic
  144390. zaraiskii
  144391. zaraiskii
  144392. structural
  144393. factors
  144394. reactivity
  144395. biphe
  144396. zarini
  144397. zarraga
  144398. zarzycki
  144399. zasshi
  144400. zassinovich
  144401. zassinovich
  144402. grazia
  144403. mestroni
  144404. giovanni
  144405. gladiali
  144406. serafino
  144407. asymm
  144408. zaugg
  144409. zavada
  144410. zavalishina
  144411. zayed
  144412. zbigniew
  144413. zbiral
  144414. zbiral
  144415. transformations
  144416. phosphorus
  144417. stabilized
  144418. anions
  144419. zdanovich
  144420. zdenek
  144421. zdero
  144422. zebovitz
  144423. zecchi
  144424. zecchi
  144425. gaetano
  144426. electrocyclic
  144427. reactions
  144428. alpha
  144429. zecchi
  144430. gaetano
  144431. chemistry
  144432. azidohydrazones
  144433. developments
  144434. zeelenY
  144435. zeelen
  144436. steroids
  144437. second
  144438. supplements
  144439. edition
  144440. zefirov
  144441. zefirov
  144442. koz'min
  144443. abramenkov
  144444. problem
  144445. tetrah
  144446. zefirov
  144447. makhon'kov
  144448. advances
  144449. chemistry
  144450. zefirov
  144451. nikolai
  144452. nikolai
  144453. beloglazkina
  144454. elena
  144455. kutatel
  144456. zehani
  144457. zehavi
  144458. zeifman
  144459. zeisig
  144460. zelewski
  144461. zelichowicz
  144462. zeller
  144463. zeller
  144464. mewes
  144465. ehninger
  144466. blanz
  144467. formation
  144468. reactive
  144469. zemskov
  144470. zemskov
  144471. zenes
  144472. zenichi
  144473. formation
  144474. benzophenanthridine
  144475. alkaloids
  144476. zenneck
  144477. zeolit
  144478. zeolite
  144479. zeolites
  144480. zerbetto
  144481. zerovalent
  144482. zetirova
  144483. zettlmeier
  144484. zgierski
  144485. zhabinskii
  144486. zhadonva
  144487. zhangR
  144488. zhdankin
  144489. zhdanov
  144490. zhdanov
  144491. alekseev
  144492. kompantseva
  144493. vergeychik
  144494. zhdanov
  144495. uzlova
  144496. glebova
  144497. ketophosphonic
  144498. zhelebva
  144499. zhengming
  144500. zhidkova
  144501. zhifu
  144502. zhilina
  144503. zhinkin
  144504. zhitang
  144505. zhivich
  144506. zhmurova
  144507. zhong
  144508. xiang
  144509. total
  144510. synthesis
  144511. antimalar
  144512. hutchins
  144513. robert
  144514. hutchins
  144515. marygail
  144516. asymmetric
  144517. zhubanov
  144518. zidovudine
  144519. ziegler
  144520. ziegler-natta
  144521. ziling
  144522. zimmer
  144523. zimmer
  144524. reinhold
  144525. alkoxyallenes
  144526. building
  144527. blocks
  144528. organic
  144529. zimmerman
  144530. zimmerman
  144531. methane
  144532. zimmerman
  144533. rearrangement
  144534. zimmerman
  144535. howard
  144536. methane
  144537. rearrangement
  144538. organic
  144539. zimmerman
  144540. molecular
  144541. tweezers
  144542. synthetic
  144543. receptors
  144544. zimmerman
  144545. steven
  144546. rigid
  144547. molecular
  144548. tweezers
  144549. hosts
  144550. zimmermann
  144551. zimmi
  144552. borohydride
  144553. reducing
  144554. agent
  144555. potential
  144556. chloride
  144557. radical
  144558. initiator
  144559. chelating
  144560. enolates
  144561. reformatsky
  144562. blaise
  144563. reactions
  144564. halide
  144565. mediated
  144566. nucleophilic
  144567. attack
  144568. thioacid
  144569. salts
  144570. promoted
  144571. reactions
  144572. cyano
  144573. group
  144574. zinc-copper
  144575. zincate
  144576. zinczuk
  144577. zines
  144578. zinin
  144579. zinner
  144580. zinsmeister
  144581. zinsmeister
  144582. dietmar
  144583. becker
  144584. eicher
  144585. theophil
  144586. bryophi
  144587. zipper
  144588. zipper-mode
  144589. zipper-mode
  144590. cascade
  144591. carbometalation
  144592. construction
  144593. zircocene
  144594. zircocene
  144595. alkene
  144596. complexes
  144597. their
  144598. formation
  144599. structure
  144600. zirconium
  144601. zirconium
  144602. catalyzed
  144603. asymmetric
  144604. carbomagnesation
  144605. zirconium
  144606. catalyzed
  144607. highly
  144608. regioselective
  144609. carbon-carbon
  144610. zirconium
  144611. catalyzed
  144612. kinetic
  144613. resolution
  144614. pyrans
  144615. zirconium
  144616. catalyzed
  144617. kinetic
  144618. resolutions
  144619. pyrans
  144620. zirconium
  144621. mediated
  144622. highly
  144623. diastereoselective
  144624. contractio
  144625. zirconium-mediated
  144626. promoted
  144627. reactions
  144628. cyano
  144629. group
  144630. zirconium
  144631. cataylzed
  144632. enantioselective
  144633. methylalumination
  144634. zirconium-mediated
  144635. highly
  144636. diastereoselective
  144637. contractio@
  144638. zollinger
  144639. nitrogen
  144640. leaving
  144641. group
  144642. dediazoniation
  144643. arom@
  144644. zweifel
  144645. chloride
  144646. allyl
  144647. silane@
  144648. alcohol
  144649. alcohol
  144650. amine@
  144651. aldehyde
  144652. alcohol
  144653. alkene
  144654. aldehyde@
  144655. amide@
  144656. aminoacid@
  144657. aniline
  144658. iodoaniline@
  144659. chloro
  144660. ether
  144661. allyl
  144662. ether@
  144663. epoxide
  144664. aldehyde@
  144665. halide@
  144666. ketone
  144667. alcohol@
  144668. zirconium-mediated
  144669. highly
  144670. diastereoselective
  144671. contractio
  144672. zirconium-promoted
  144673. zirconium-promoted
  144674. bicyclization
  144675. enynes
  144676. zirconoceneF
  144677. zirconocene
  144678. compleses
  144679. unsaturated
  144680. organic
  144681. molecules
  144682. zirconocene-alkene
  144683. zirconocene-alkene
  144684. complexes
  144685. their
  144686. formation
  144687. structure
  144688. zirconocene-derived
  144689. zirconocenes
  144690. zirconocenyl
  144691. ziyang
  144692. zlatkis
  144693. zlomskii
  144694. zlotin
  144695. zlotin
  144696. luk'yanov
  144697. regioselective
  144698. methods
  144699. synthesis
  144700. zlotskii
  144701. zlotsky
  144702. zn2cl6
  144703. znbr2
  144704. catalysed
  144705. versus
  144706. cycloaddition
  144707. allyltrime
  144708. zobova
  144709. zoellner
  144710. zofia
  144711. zoller
  144712. zoller
  144713. three
  144714. membered
  144715. rings
  144716. containing
  144717. sulfur
  144718. small
  144719. zollinger
  144720. zollinger
  144721. color
  144722. chemistry
  144723. syntheses
  144724. properties
  144725. applica
  144726. zollinger
  144727. nitrogen
  144728. leaving
  144729. group
  144730. dediazoniation
  144731. zolotukhina
  144732. zolotukhina
  144733. krutikov
  144734. lavrent'ev
  144735. derivatives
  144736. zoltewicz
  144737. zoltewicz
  144738. deady
  144739. quaternization
  144740. heteroaromatic
  144741. zomalonic
  144742. zomer
  144743. zorin
  144744. zorkii
  144745. zouhair
  144746. zschage
  144747. zsolt
  144748. zubarev
  144749. zubarev
  144750. belevskii
  144751. bugaenko
  144752. trapp
  144753. zubkov
  144754. zubrick
  144755. zubrick
  144756. james
  144757. organic
  144758. survival
  144759. manual
  144760. stude
  144761. zuckermann
  144762. zufan
  144763. zuman
  144764. zuman
  144765. addition
  144766. reduction
  144767. oxidation
  144768. reactions
  144769. zupan
  144770. zupan
  144771. photochemistry
  144772. fluorosubstituted
  144773. aromatic
  144774. zurabyan
  144775. zurita
  144776. zverev
  144777. zverev
  144778. kitaev
  144779. photoelectron
  144780. spectroscopy
  144781. zvezdina
  144782. zvolinskii
  144783. zvonkova
  144784. zwanenburg
  144785. zweifel
  144786. zweifel
  144787. zweifel
  144788. versatile
  144789. alkenylalanes
  144790. alkenylboranes
  144791. zwittazido
  144792. zwitterionic
  144793. zwitterionic
  144794. rhodium
  144795. complex
  144796. catalyzed
  144797. silylhydroformy
  144798. zwitterions
  144799. zwitterions
  144800. diradicals
  144801. zybill
  144802. zybill
  144803. christian
  144804. handwerker
  144805. hermann
  144806. friedrich
  144807. holger
  144808. silaorg
  144809. 13-diene
  144810. 13-diene
  144811. 14-diene
  144812. 14-diene
  144813. acetal
  144814. acetal
  144815. furan
  144816. acetal
  144817. cyclic
  144818. ether
  144819. acetate
  144820. acetylene
  144821. acetylene
  144822. alkene
  144823. acetylene
  144824. allene
  144825. acetylene
  144826. enyne
  144827. acetylene
  144828. alkene
  144829. acetylenic
  144830. acetylenic
  144831. ketone
  144832. alcohol
  144833. acetylenic
  144834. ketone
  144835. enone
  144836. aldehyde
  144837. alcohol
  144838. aldehyde
  144839. alkene
  144840. aldehyde
  144841. alkyne
  144842. alcohol
  144843. aldehyde
  144844. benzyl
  144845. alcohol
  144846. aldehyde
  144847. diene
  144848. aldehyde
  144849. aldehyde
  144850. ether
  144851. aldehyde
  144852. homoallylic
  144853. alcohol
  144854. aldehyde
  144855. homoallylic
  144856. alcohol
  144857. ether
  144858. aldehyde
  144859. ketone
  144860. alkene
  144861. aldehyde
  144862. alcohol
  144863. aldehyde
  144864. homoallylic
  144865. alcohol
  144866. aldehyde
  144867. ketone
  144868. aldehyde
  144869. vinyl
  144870. boronic
  144871. ester
  144872. alkane
  144873. alkane
  144874. cyclopropane
  144875. alkene
  144876. alkene
  144877. alcohol
  144878. amide
  144879. amide
  144880. amine
  144881. amide
  144882. ketone
  144883. amine
  144884. amine
  144885. lactam
  144886. odoaniline
  144887. arene
  144888. amide
  144889. iodoaryl
  144890. amide
  144891. aryllithium
  144892. bromide
  144893. alcohol
  144894. bromide
  144895. amine
  144896. halide
  144897. ether
  144898. silane
  144899. phenol
  144900. aryllithium
  144901. azide
  144902. azide
  144903. amine
  144904. azide
  144905. isocyanate
  144906. amide
  144907. azide
  144908. lactam
  144909. azido
  144910. aziridine
  144911. b-ketophosphine
  144912. b-ketophosphine
  144913. oxide
  144914. alkene
  144915. benzyl
  144916. boronic
  144917. bromide
  144918. bromoalcohol
  144919. bromoalcohol
  144920. epoxide
  144921. bromoketone
  144922. bromoketone
  144923. bromoalcohol
  144924. carbamate
  144925. carbamate
  144926. amine
  144927. carbonate
  144928. carboxylic
  144929. chloride
  144930. chloro
  144931. chloro
  144932. acetal
  144933. epoxide
  144934. aldehyde
  144935. epoxide
  144936. tetrahydrofuran
  144937. epoxide
  144938. azido
  144939. alcohol
  144940. epoxide
  144941. unsaturated
  144942. ketone
  144943. epoxy
  144944. epoxy
  144945. ketone
  144946. ester
  144947. ester
  144948. ester
  144949. alcohol
  144950. ester
  144951. amide
  144952. ester
  144953. cyclopropanol
  144954. ester
  144955. ether
  144956. ester
  144957. ketone
  144958. ester
  144959. ketone
  144960. alcohol
  144961. ester
  144962. lactone
  144963. ester
  144964. lactone
  144965. ether
  144966. ether
  144967. furan
  144968. imine
  144969. amine
  144970. indole
  144971. indole
  144972. indolone
  144973. indole
  144974. oxindole
  144975. indolone
  144976. iodide
  144977. iodoaniline
  144978. iodoaryl
  144979. isocyanate
  144980. ketoaldehyde
  144981. ketoaldehyde
  144982. ketone
  144983. oxide
  144984. oxime
  144985. oxime
  144986. amine
  144987. oxindole
  144988. peroxide
  144989. phenol
  144990. phenol
  144991. ketophenol
  144992. propargyl
  144993. propargyl
  144994. alcohol
  144995. silane
  144996. solfone
  144997. stannane
  144998. stannyl
  144999. stannyl
  145000. acetal
  145001. carboxylic
  145002. triflate
  145003. triflate
  145004. alkene
  145005. unsaturated
  145006. unsaturated
  145007. lactone
  145008. lactone
  145009. vinyl
  145010. vinyl
  145011. iodide
  145012. allylic
  145013. alcohol
  145014. vinyl
  145015. iodide
  145016. ketone
  145017. vinyl
  145018. iodide
  145019. allylic
  145020. alcohol
  145021. vinyl
  145022. sulfone
  145023. alkene
  145024. diene
  145025. ch3nh
  145026. ADDRESS
  145027. ALPHA
  145028. AUTHOR
  145029. BOOLEAN
  145030. CARD NUMBER
  145031. D    CHECKPASS
  145032. CREATED BY
  145033. CREATED ON
  145034. CREATOR
  145035. FILES
  145036. FUNCTIONAL GROUPS
  145037. GOTO SEARCH PAGE
  145038. GRAPHICMARKER
  145039.     KEYWORD 1
  145040. LINKS
  145041. LOCATION
  145042. NEW CARD
  145043. NEW PASS
  145044. u    NEXT CARD
  145045. NOTES
  145046. NUMBER
  145047. OLD PASS
  145048. OWNER
  145049. PASS2
  145050. PERFORM SEARCH
  145051. PREVIOUS CARD
  145052. PRINT?
  145053. ?    REFERENCE
  145054. REFNAME
  145055. REFPAGE
  145056. 6    REFSEARCH
  145057. REFYEAR
  145058. SCREEN PREFS
  145059. SEARCH DATE
  145060. SEARCH TERM 2
  145061. SEARCH TERM 3
  145062. SEARCH TERM 4
  145063. SEARCH TERM 5
  145064. SEARCH TERMS
  145065. SEARCHANDOR
  145066. SEARCHANDOR2
  145067. SEARCHANDOR3
  145068. SEARCHPREFS
  145069. SEARCHRESULTS PREFS
  145070. SEARCHTERM
  145071. SEARCHVARIABLE
  145072. SEARCHVARIABLE COPY
  145073. SEARCHVARIABLE COPY2
  145074. SEARCHVARIABLE1
  145075. SEARCHVARIABLE10
  145076. SEARCHVARIABLE11
  145077. SEARCHVARIABLE12
  145078. SEARCHVARIABLE13
  145079. SEARCHVARIABLE14
  145080. SEARCHVARIABLE15
  145081. SEARCHVARIABLE2
  145082. SEARCHVARIABLE3
  145083. SEARCHVARIABLE4
  145084. SEARCHVARIABLE5
  145085. SEARCHVARIABLE6
  145086. Sunday
  145087. Monday
  145088. Tuesday
  145089.     Wednesday
  145090. Thursday
  145091. Friday
  145092. Saturday
  145093. January
  145094. February
  145095. March
  145096. April
  145097. August
  145098.     September
  145099. October
  145100. November
  145101. December
  145102. 1st Quarter
  145103. 2nd Quarter
  145104. 3rd Quarter
  145105. 4th Quarter
  145106. 6/2/966
  145107. Cards
  145108. Credits
  145109. Cards Help
  145110. Search Help
  145111. Search List
  145112. Search List w/ Structures
  145113. Splash
  145114. 12" Monitor
  145115. 17" Monitor
  145116. Field Help
  145117. Import/Export Help
  145118. Globals
  145119. Master Search
  145120. Preferences
  145121. 17" Monitor UnReg
  145122. 12" Monitor Un-Registered
  145123. Cards Un-Registered
  145124. Pass Confirm
  145125. Master Form Search
  145126. Theilheimer Help
  145127. Search List w/ StructuresUnreg
  145128. Search ListUnreg
  145129. Registration
  145130. A    Passwords
  145131. Brakpuhr
  145132. CardsB
  145133. SEARCHVARIABLE7
  145134. SEARCHVARIABLE8
  145135. SEARCHVARIABLE9
  145136. SEARCHYESNO
  145137. SEARCHYESNO2
  145138. SEARCHYESNO3
  145139. SITES
  145140. SPLASH PREFS
  145141. l    STRUCTURE
  145142. SYNTHON
  145143. SYNTHON SEARCH
  145144. THIELBREAK
  145145. H    THIELFORM
  145146. THIELHEIMER
  145147. Z    THIELTYPE
  145148. THIELTYPE2
  145149. THIELTYPE3
  145150. THIELTYPE4
  145151. THIELTYPE5
  145152. TITLE
  145153.     TRANSFORM
  145154. UNREG
  145155. USER PREFS
  145156. VIEW PREFS
  145157. WEB CONNECTIONS
  145158. AuthorB
  145159. A    ReferenceB
  145160. A    Keyword 1B
  145161.     A    StructureB
  145162. NotesB
  145163. LinksB
  145164. 22646
  145165. Created OnB
  145166. Goto Search PageB
  145167. New CardB
  145168. A    Next CardB
  145169. Previous CardB
  145170. Perform SearchB
  145171. TitleB
  145172. YearB
  145173. PageB
  145174. Number
  145175. FilesB
  145176. Search TermsB
  145177. Created ByB
  145178. Gabriel Weatherhead
  145179. GABRIEL WEATHERHEAD
  145180. BooleanB
  145181. Search Term 2B
  145182. Search Term 3B
  145183. Search Term 4B
  145184. Search Term 5B
  145185. 3A    refsearchB
  145186. refyearB
  145187. refnameB
  145188. refpageB
  145189. Functional GroupsB
  145190. 8A    TransformB
  145191. LocationB
  145192. synthonB
  145193. Synthon SearchB
  145194. Print?B
  145195. OwnerB
  145196. Card NumberB
  145197. 21638
  145198. Search DateB
  145199. FA    thielformB
  145200. GA    thieltypeB
  145201. thielbreakB
  145202. thieltype2B
  145203. thieltype3B
  145204. thieltype4B
  145205. thieltype5B
  145206. searchandorB
  145207. searchvariable1B
  145208. searchvariable2B
  145209. searchvariable3B
  145210. searchyesnoB
  145211. searchyesno2B
  145212. searchyesno3B
  145213. thielheimerB
  145214. F &  
  145215. G &  
  145216. searchvariableB
  145217. searchandor2B
  145218. searchandor3B
  145219. searchvariable4B
  145220. searchvariable5B
  145221. searchvariable6B
  145222. searchvariable7B
  145223. searchvariable8B
  145224. searchvariable9B
  145225. searchvariable CopyB
  145226. searchvariable Copy2B
  145227. searchvariable10B
  145228. searchvariable11B
  145229. searchvariable12B
  145230. searchvariable13B
  145231. searchvariable14B
  145232. searchvariable15B
  145233. splash prefsB
  145234. screen prefsB
  145235. user prefsB
  145236. searchresults prefsB
  145237. view prefsB
  145238. creatorB
  145239. passB
  145240. pass2B
  145241. new passB
  145242. old passB
  145243. searchprefsB
  145244. web connectionsB
  145245. sitesB
  145246. addressB
  145247. betaB
  145248. alphaB
  145249. searchtermB
  145250. graphicmarkerB
  145251. unregB
  145252. A    checkpassB
  145253. indolen
  145254. splash
  145255. Gabriel Weatherhead
  145256. list w/ structure
  145257. proteus
  145258. Button
  145259. Tetrahedron
  145260. CreditsB
  145261. Go BackaUIf you have any ideas you would like to see implemented, please let me know via email
  145262.     ...
  145263. Invalid Date    
  145264. View as Listk    Vol : No.l
  145265. pagem
  145266. Synthonsn
  145267. Fileso
  145268. Locationq
  145269. Transformationr
  145270. Titlev
  145271. Notesw
  145272. Keywordsz
  145273. Gabriel Weatherhead|
  145274. Created By
  145275. entered by:
  145276. Thielheimer
  145277. Owner:
  145278. Credits
  145279. vI would like to thank the people that helped with testing this new release as well as providing references and ideas.
  145280. John Dankwardt (The Referencc Maniac that entered the majority of the references)
  145281. Sharon Dankwardt (Supplier of many ideas for the program and interface as well as                  references)
  145282. Jacob Berger (Testing and helped with port to PC)
  145283. Brad Loe
  145284. Leon Lin
  145285. Cards HelpB
  145286. Gabriel.Weatherhead@syntex.com
  145287. This reference program was created by Gabriel Weatherhead on Filemaker Pro (copyright Claris Software). The initial idea, as well as the initial 800 references for this program were provided by  John & Sharon Dankwardt. Any distribution of this software is encouraged as long as the initial database is not altered in any way. Please feel free to change any aspect of this database (I hate those FileMaker records that lock you out of the Layout editing. That
  145288. s the best part of FileMaker.). Bucopyright Claris Software). The initial idea, as well as the initial 800 references for this program were provided by  John & Sharon Dankwardt. Any distribution of this software is encouraged as long as the initial database is not altered in any way. Please feel free to change any aspect of this database (I hate those FileMaker records that lock you out of the Layout editing. That
  145289. s the best part of FileMaker.). Bu
  145290. t please, please, please only distribute the original file. If you want to share your references, export them and distribute the file. If you use this program, all that I ask is to send me your references via email. Export your records to a text file and email the file to me with a note about which export method you used. Even if you do not send references, I would still like to see how many people use this program. Please email me anyway.  Thanks for supporting SEMI-FREEWARE!
  145291. Search HelpB
  145292. Click the Help Topic BelowjVGrow and shrink Buttons. These take you between normal, small, and large monitor mode.l
  145293. Go Back To Cardsm
  145294. The Date Created field is for your information only. The program places the date that the BLANK card was created in the box automatically.
  145295. Click the Help Topic BelowjVGrow and shrink Buttons. These take you between normal, small, and large monitor mode.l
  145296. Go Back To Cardsm
  145297. The Date Created field is for your information only. The program places the date that the BLANK card was created in the box automatically.
  145298. The ID field can not and should not be altered. This is used by the program for record keeping. Each new card is assigned a unique ID when it is created. The ID number is no indication of the card number however.p
  145299. Static Fieldsq
  145300. Delete current card|
  145301. Create blank card}
  145302. Go forward one card~
  145303. Go back one card
  145304. Goto front of stack
  145305. Goto end of stack
  145306. A>Not surprisingly, this button prints the card you are viewing.
  145307. This button takes you to the searching page. The type of search page is determined by the preference setting you have chosen. See Search Help Above for more help on Searching.
  145308. This button refinds all of the cards after search results have been viewed. It
  145309. s just an alternative to using the menu command.
  145310. The Buttons
  145311. Press the pencil button
  145312. GfPress the 
  145313.  button on the button pad to create a new blank card.
  145314. Fill in all the pertinent fields.
  145315. Creating a card
  145316. JNThis button takes you to the preferences page to adjust your personal settings
  145317. This button activates Netscape and connects to the site chosen in the menu. You MUST have applescript installed for this to work.
  145318. Fields
  145319. N    Searching
  145320. Theilheimer
  145321. Import / Export
  145322. Free Registration
  145323. Un takes you to the preferences page to adjust your personal settings
  145324. This button activates Netscape and connects to the site chosen in the menu. You MUST have applescript installed for this to work.
  145325. Fields
  145326. N    Searching
  145327. Theilheimer
  145328. Import / Export
  145329. Free Registration
  145330. 8These are used to easily enter special characters. Place the cursor where you would like the character and press either the beta or the pi button to insert the character. The alpha character is not a button , but rather a field to copy and paste from. Feel free to enter any other special characters in this box.
  145331. Search ListB
  145332. gjEnter the date criteria and click the search button. This ONLY searches the creation dates of the records.h
  145333. Date Searchi
  145334. Go To Searchj
  145335. Go Back To Helpk
  145336. If you have already performed a search, and another search is started, all previous results will be lost.
  145337. There is no subset searching. This means you can not narrow down the search hits by doing another search.l
  145338. Limitations
  145339. gjEnter the date criteria and click the search button. This ONLY searches the creation dates of the records.h
  145340. Date Searchi
  145341. Go To Searchj
  145342. Go Back To Helpk
  145343. If you have already performed a search, and another search is started, all previous results will be lost.
  145344. There is no subset searching. This means you can not narrow down the search hits by doing another search.l
  145345. Limitations
  145346. Functional Group Transformation
  145347. 1the Transformation box of the cards. If your records contain multiple transformations, which is sometimes necessary, and you wish to find an exact Transformation, enter the search data as below:
  145348. aldehyde -> alcohol
  145349. with the quotes. If you wish to simply find all transformation that contain the term aldehyde, then enter as follows:
  145350. aldehyde
  145351. with NO quotes. This will find all records that contain the term aldehyde, regardless of whether it is the starting or enBZding point. If you want the aldehyde as a product then enter in this manner:
  145352. -> aldehyde
  145353. Functional Group Transformation
  145354. Searching Tipst
  145355. Form Search
  145356. This search format has the most versatility, however, it is more complex to use. Enter the term you wish to look for in one of the boxes. If you want to look for the term in any of the fields, then:
  145357. If you want to search in a particular field
  145358. 1)  Type the term in the green Box in the upper left field
  145359. 2)  Press the button corresponding to the field you want searched
  145360. 3)  Press the search button
  145361. If you want to look for a term in any field
  145362. 1)  Type the term in the green Box in the upper le
  145363. Jft corner
  145364. 2)  Press the 
  145365. Any Field
  145366.  button. Search requests will then be created
  145367. 3)  Press the search button
  145368. If you want to look for one term but NOT another then:
  145369. 1)  Follow above directions
  145370. 2)  Press the 
  145371.  button
  145372. 3)  Type the word to exclude from the results. (optionally press the 
  145373. Any Field
  145374. 4)  Press the search button
  145375. Theilheimer Codesx
  145376. Enter the code just as you would like the result to appear. Optionally leaving out either the bond formed or broken as well as the type of reaction. See the corresponding Help section for the code definitions.y
  145377. Deletes Queryz
  145378. Cancels Search{    ID Search|
  145379. This searches for the Card ID}
  145380. Performs Search~
  145381. Adds New Search
  145382. Boolean  Search
  145383. This is the most simple search method.  Another advantage is that the List View contains the term used for searching in its header
  145384. 1) Enter the term to search for in the box. 
  145385. 2) If you have no other criteria then check the 
  145386.  button below the term. If you want another term to exist within the found set, check the 
  145387.  button. If another term can be substituted, check the 
  145388.  button.
  145389. 3) Check the fields that you would like to have searched to the right of the search terms.
  145390. 4) PerforBKm the search
  145391. The search term format for the Form Search applies here also.
  145392. D9NOTE: The 
  145393.  search automatically searches all fields.
  145394. Go Back To Help
  145395. Go To Search
  145396. Search List w/ StructuresB
  145397. Find Marked\
  145398. Include Graphic]
  145399. Unmark Records^
  145400. Print Records_
  145401. Print Marked`
  145402. Printa
  145403. Search Termsb
  145404. Files:d
  145405. Pagee
  145406. Card IDg
  145407. Keywordsh
  145408. Journalj
  145409. Title / Authort
  145410. Go To Default View
  145411. SplashB
  145412. Exclude Graphic\
  145413. Unmark Records]
  145414. Print Records^
  145415. Print Marked_
  145416. Print`
  145417. Search Termsa
  145418. Files:c
  145419. Paged
  145420. CardIDf
  145421. Keywordsg
  145422. Yearh
  145423. Journali
  145424. Title / Authorn
  145425. Go To Default View
  145426. 12" MonitorB
  145427. AgreeB
  145428. CreditsC
  145429. HelpD
  145430. V. 3.0E
  145431. SYNTHETIC REFERENCESF/In Essence: I don
  145432. t profit so you won
  145433. t profit!G_Reproduction of this database  (excluding graphics) for resale purposes is strictly prohibited.HSLimited use is permitted, barring sale or trade of this database for personal gain.I
  145434. Chemdraw Copyright CSC SoftwareJ(File Maker Pro Copyright Claris SoftwareKfAll Ideas, scripts, and layouts pertained herein are the intellectual property of Gabriel Weatherhead.L%COPYRIGHT 1996 By Gabriel WeatherheadM"An Organic Chemists Reference ToolR
  145435. UnlockS
  145436. PrefsU
  145437. Distribution of the original UNALTERED database is permitted. Distributing a modified version is permitted only by explicit agreement with the author.VeThe author is not responsible for the content of the database, nor any damage incurred during its useference ToolR
  145438. UnlockS
  145439. PrefsU
  145440. Distribution of the original UNALTERED database is permitted. Distributing a modified version is permitted only by explicit aggreement with the author.
  145441. 17" MonitorB
  145442. Gabriel Weatherhead|
  145443. Created By
  145444. Created By
  145445. Gabriel Weatherhead
  145446. Keywords
  145447. Notes
  145448. Title
  145449. Transformation
  145450. Help Me
  145451. Location
  145452. Files
  145453. Synthons
  145454.     Vol : No.
  145455. View as List
  145456. entered by:
  145457. Owner:
  145458. Field HelpB
  145459. Yesf)x
  145460. Owner:k    Vol : No.l
  145461. pagem
  145462. Synthonsn
  145463. Fileso
  145464. Locationq
  145465. Transformationr
  145466. Notesw
  145467. Keywordsz
  145468. Gabriel Weatherhead|
  145469. Created By
  145470. Thielheimer
  145471. entered by:
  145472. Created By Gabriel Weatherhead
  145473. Import/Export HelpB
  145474. Go Back To Help
  145475. Go Back To Help
  145476. This box is to specify the owner of the database.  This filed is printed with the reference, so that the recipient will recognize the source at a later date. Feel free to change this box by entering the layout mode and typing a new name.C    Owner BoxD
  145477. The Date Created field is for your information only. The program places the date that the BLANK card was created in the box automatically.
  145478. The ID field can not and should not be altered. This is used by the program for record keeping. Each new card is assigned a unique ID when it is created. The ID number is no indication of the card number however.F
  145479. Static FieldsG
  145480. These are pull down menus. Simply click and hold to get a listing of the most common Journals. Select the pertinent journal. If the Journal name is not present, simply select 
  145481. Other...
  145482.  and type the name. The date field operates similarlyH
  145483. Journal Fields
  145484. This box is a pointer to where the paper is in your personal files. This box is generally not used for searching, therefore it is personal preference as to the format.J
  145485. The Files BoxK
  145486. This box is used to record the Umpoled Synthons pertinent to the reference. Again, the format is not important, as long as you are consistent. I use the the format 
  145487. The Synthons Box
  145488. yUse this box to specify the particular type of transformation. This area may be searched independently of the other areas thus making a quick transformation search possible. Some of the references already contain this information. The format of the information is not important, as long as you are consistent throughout the entire stack. I use the format 
  145489. aldehyde -> alcohol
  145490. The Transformation BoxO
  145491. Created By Box
  145492. Location BoxR
  145493. This refers to the University or Corporation that the Author is representing. This field is for personal use only. It is not searchable.
  145494. is field is for personal use only. It is not searchable.
  145495. GlobalsB
  145496. A*Importing and Exporting in Generic Formats
  145497. ]Example: Transfer a weeks worth of record entries from home to work. Perform a 
  145498. Find Date
  145499.  with the date as 
  145500. >10/20/95
  145501. . Save a blank database to a floppy. Open the blank database. Use the Import command from the 
  145502.  menu. Choose the database file in which you performed the 
  145503. Find Date
  145504.  Click the 
  145505. Match Fields
  145506.  button. Click Import. You
  145507. re Done.
  145508. The superior method for transferring a small number of records (i.e. between home and work) is to create a blank database and import the desired records into it.D
  145509. Importing And ExportingE
  145510. Go Back To Helpase file in which you performed the 
  145511. Find Date
  145512.  Click the 
  145513. Match Fields
  145514.  button. Click Import. You
  145515. re Done.
  145516. The superior method for transferring a small number of records (i.e. between home and work) is to create a blank database and import the desired records into it.D
  145517. Importing And ExportingE
  145518. Go Back To Help
  145519. Go to the import option under the menu item 
  145520. . Choose the file format to import from and then perform the import. Make sure to match the fields before importingG
  145521. To Import RecordsHbPerform a Find in the standard way, and then simply use the Export menu under the main menu 
  145522. To Export Found Records
  145523. Master SearchB
  145524. Yesf)x
  145525. Yesf)x
  145526. Yesf)x
  145527. Yesf)x
  145528. Yesf)x
  145529. pass2V
  145530. betaX
  145531. alpha\
  145532. pass2V
  145533. betaX
  145534. alpha\
  145535. Untitled preferences-2
  145536. count
  145537. currentpoint 192837465
  145538. currentpoint
  145539. save/chemsave exch def
  145540. %%BeginProcSet: chemdict30 24 10
  145541. % ChemDraw Laser Prep
  145542. % Copyright 198
  145543. 6-1993, Cambridge Scientific Computing, Inc.
  145544. userdict/chemdict30 210 dict put
  145545. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  145546. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  145547. PreferencesB
  145548. Search Term(s)~
  145549. Fields To Search
  145550. Title
  145551. Author
  145552. Keywords
  145553. Notes
  145554. Synthon
  145555. Title
  145556. Author
  145557. Keywords
  145558. Notes
  145559. x    Transform
  145560. Synthon
  145561. {    Transform
  145562. Cancel Search
  145563. Perform
  145564. 17" Monitor UnRegB
  145565. Yesf)x
  145566. Change PasswordQ
  145567. Old PasswordR
  145568. New PasswordV
  145569. Method of Searching:W
  145570. Unlock DatabaseX
  145571. Open Database To:Y
  145572. Monitor Setting:Z
  145573. Database Owner:[
  145574. Show Search Results As:]
  145575. Password Verification
  145576. Change PasswordQ
  145577. Old PasswordR
  145578. New PasswordV
  145579. Method of Searching:W
  145580. Unlock DatabaseX
  145581. Open Database To:Y
  145582. Monitor Setting:Z
  145583. Database Owner:[
  145584. Show Search Results As:]
  145585. Password Verification
  145586. 12" Monitor Un-RegisteredB
  145587. Yesf)x
  145588. Gabriel Weatherhead|
  145589. Created By
  145590. UN-REGISTERED COPY
  145591. Created By
  145592. Gabriel Weatherhead
  145593. Keywords
  145594. Notes
  145595. Transformation
  145596. Location
  145597. Files
  145598. Synthons
  145599.     Vol : No.
  145600. Owner:
  145601. Thielheimer
  145602. entered by:
  145603. UNREGISTERED COPY
  145604. SEE HELP FOR FREE REGISTRATION
  145605. EE HELP FOR FREE REGISTRATION
  145606. CSC ChemDraw will be opened automatically and a new window will be created.
  145607. Draw the reaction or structure as normal.
  145608. Select all
  145609. Switch back to File Maker Pro
  145610. Press the continue button to the left of the card.
  145611. The structure will be automatically sized and pasted.
  145612. Cards Un-RegisteredB
  145613. Created By
  145614. Gabriel Weatherhead
  145615. Author
  145616. Keywords
  145617. Notes
  145618. Title
  145619. Transformation
  145620. Help Me
  145621. Location
  145622. Files
  145623. Synthons
  145624. ]    Vol : No.
  145625. View as List
  145626. entered by:
  145627. Owner:
  145628. UN-REGISTERED COPY
  145629. SEE HELP FOR FREE REGISTRATION
  145630. Pass ConfirmB
  145631. confirmD$Please Confirm Registration PasswordE
  145632. You only have to do this onceG    forget it
  145633. Gabriel Weatherhead|
  145634. Created By
  145635. UN-REGISTERED COPY
  145636. SEE HELP FOR FREE REGISTRATION
  145637. Created By
  145638. Gabriel Weatherhead
  145639. Keywords
  145640. Notes
  145641.     ...
  145642. Invalid Date    
  145643. Title
  145644. Transformation
  145645. Location
  145646. Files
  145647. Synthons
  145648.     Vol : No.
  145649. View as List
  145650. entered by:
  145651. Thielheimer
  145652. Owner:
  145653. Master Form SearchB
  145654. Theilheimer HelpB
  145655.     Any Field
  145656. Entry Date
  145657. Thielheimer
  145658. Transformation
  145659. Synthons
  145660. Title
  145661. Author
  145662. Keywords
  145663. Notes
  145664. New Item
  145665. Cancel Search
  145666. Perform
  145667. Search List w/ StructuresUnregB
  145668. Go Back To Help
  145669. The Theilheimer reaction code is adopted from a series of books cataloging reactions according to the bonds breaking and forming in a reaction. I have attempted to institute this method so as to make reaction searching easier. Unfortunately I made this modification after the database was assembled. This means that almost none of the references have the Theilheimer code associated with them. On the positive side, to assign a code you simply use the pull down menus provided.
  145670. The Theilheimer Wayo
  145671. This new category allows for powerful cataloging and searching features based on the type of reaction presented. Feel free to reader further about Theilheimer codes and the set of books published by KARGER publishers.
  145672. 1eaction presented. Feel free to reader further about Theilheimer codes and the set of books published by KARGER publishers.
  145673. r    The Codes
  145674. Indicates an ADDITION reaction
  145675. <A!Indicates an ELIMINATION reaction
  145676. Indicates an EXCHANGE reaction
  145677. >A"Indicates a REARRANGEMENT reaction
  145678. >A"Indicates a REARRANGEMENT reaction
  145679. Search ListUnregB
  145680. Exclude Graphic\
  145681. Unmark Records]
  145682. Print Records^
  145683. Print Marked_
  145684. Print`
  145685. Search Termsa
  145686. Files:c
  145687. Paged
  145688. CardIDf
  145689. Keywordsg
  145690. Yearh
  145691. Journali
  145692. Title / Authorj
  145693. Un-Registered Copyk
  145694. See Help for Free Registrationn
  145695. Go To Default View
  145696. RegistrationB
  145697. Find Marked\
  145698. Include Graphic]
  145699. Unmark Records
  145700. Print Records_
  145701. Print Marked`
  145702. Printa
  145703. Search Termsb
  145704. Files:c
  145705. Go To Default Viewd
  145706. Pagee
  145707. Card IDg
  145708. Keywordsh
  145709. Yeari
  145710. Journalj
  145711. Title / Authorr
  145712. Un-Registered Copys
  145713. See Help for Free Registration
  145714. )A    PasswordsB
  145715. To Unlock:B71)  Goto the preferences.
  145716. 2)  Click the 
  145717. Unlock
  145718.  ButtonCn3)  Type in the registration password
  145719. 4)  Click the 
  145720. Confirm
  145721.  button
  145722. 5)  Follow the instructions that  follow.
  145723. BrakpuhrB
  145724. Yesf)x
  145725. Registration is free for anyone in academics. Professors, instructors, Students, Postdocs, Personnel. The origin of your email (i.e. the return address) will be proof of affiliation. BMRegistration is $15.00 for any non-academics.  Please make checks payable to:C
  145726. Once your check is received, I will mail it off to Project Seed and email (or postal mail) you the password to unlock all of the features of the database.D%EMAIL: gabriel.weatherhead@syntex.comF8Email your request for registration to the address belowG
  145727. Go Back To Help
  145728. dThe registration fee will be forwarded to the American Chemical Societies Project Seed which helps underprivileged high school students experience a summer of chemistry. I receive no part of this money. My payment is your contribution to the program. If you have any questions about Project Seed, please call the American Chemical Society at 1-800-333-9511
  145729. PROJECT SEED
  145730. ROSSI RB
  145731. ORG PREP PROCEDURE INTM
  145732. 6015N
  145733. 2/28/96V
  145734. PALLADIUM
  145735.  AND/OR COPPER
  145736. MEDIATED CROSS
  145737. COUPLING REACTIONS BETWEEN 1
  145738. ALKYNES AND VINYL, ARYL, 1
  145739. ALKYNYL, 1,2
  145740. PROPADIENYL, PROPARGYL AND ALLYLIC HALIDES OR RELATED COMPOUNDS. A REVIEWW
  145741. 1995 APRX
  145742.  27(2)a
  145743. GABRIEL WEATHERHEAD
  145744. FELDMAN B
  145745. SYNLETTCGCYCLOPROPANE VINYL RADICAL ADDITION THIO OXYGEN DIOL REVIEW OXYGENATIONM
  145746. 6016N
  145747. 2/28/96VYTHE OXYGENATION OF VINYLCYCLOPROPANES AS AN ENTRY INTO STEREOSELECTIVE 1,3-DIOL SYNTHESISW
  145748. 1995 P 217a
  145749. GABRIEL WEATHERHEAD
  145750. J ORG CHEMCRYAMAMOTO EPOXIDE AMINE PAYNE REARRANGEMENT AZIRIDINE INTRODUCTION REVIEW SHARPLESSM
  145751. 6017N
  145752. 2/28/96VbAZA PAYNE REARRANGEMENT OF ACTIVATED 2-AZIRIDINE METHANOLS AND EPOXY AMINES UNDER BASIC CONDITIONSW
  145753. VOL 60 1995 P 2044a
  145754. GABRIEL WEATHERHEAD
  145755. SYNLETTCaHANZAWA SYNLETT ZIRCONIUM ZIRCOCENE ALLYL ADDITION ALKENE METAL ORGANOMETALLIC ZIRCONOCENE REVIEWM
  145756. 6018N
  145757. 2/28/96
  145758. EnterC!Please confirm the Password belowE
  145759. Leave blank for Limited Access
  145760. indole|
  145761. indolew
  145762. indoleV
  145763. indole3
  145764. indoleC
  145765. indoleK
  145766. indole|
  145767. indolew
  145768. indoleV
  145769. indole
  145770. indole3
  145771. indoleK
  145772. indole|
  145773. indolew
  145774. indoleV
  145775. indole
  145776. indole
  145777. indole3
  145778. indole|
  145779. indolew
  145780. indole
  145781. indole
  145782. indole
  145783. indole
  145784. indole3
  145785. indole
  145786. indole
  145787. indole
  145788. indole
  145789. indole
  145790. indole|
  145791. indole3
  145792. A    disulfide|
  145793. indole
  145794. C    disulfide|
  145795. indole
  145796. K    disulfide|
  145797. indole
  145798. indoledisulfide
  145799. w    disulfide|
  145800. indole
  145801. V    disulfidew
  145802. indole
  145803.  A    disulfidew
  145804. indole
  145805. !C    disulfidew
  145806. indole
  145807. "K    disulfidew
  145808. indole
  145809. indole|    disulfide
  145810. indoledisulfide
  145811. VAFORMATION OF CARBON-CARBON BONDS USING ZIRCONOCENE BUTENE COMPLEXW
  145812. 1995 P 299a
  145813. GABRIEL WEATHERHEAD
  145814. SYNLETTCTKATSUKI CHIRAL EPOXIDE EPOXIDATION SALEN MANGANESE ASYMMETRIC CATALYST REVIEW ALKENEM
  145815. 6019N
  145816. 2/28/96VUMANGANESE SALEN CATALYZED ASYMMETRIC EPOXIDATION OF CONJUGATED TRISUBSTITUTED OLEFINSW
  145817. 1995 P 197a
  145818. GABRIEL WEATHERHEAD
  145819. CHEM COMMUNCJMAYORAL EPOXIDE EPOXIDATION METAL ORGANOMETALLIC CATALYZED REVIEW TITANIUMM
  145820. 6020N
  145821. 2/28/96VgA NEW TITANIUM SILICA CATALYST FOR 5THE EXPOXIDATION OF NON-FUNCTIONALIZED ALKENES AND ALLYLIC ALCOHOLSW
  145822. 1995 P 539a
  145823. GABRIEL WEATHERHEAD
  145824. J ORG CHEMCyJORGENSON COMPUTER INTRODUCTION REVIEW FELKIN
  145825. ANH CRAM DIASTEREOSELECTIVE STEREOCHEM COURSE BURGI DUNITZ TRAJECTORY CAMEOM
  145826. 6021N
  145827. 2/28/96VJDIASTEREOSELECTIVE ADDITIONS USING CAMEO CRAM
  145828. S RULE 
  145829.  ASYMMETRIC ADDITIONW
  145830. VOL 60 1995 P 490a
  145831. GABRIEL WEATHERHEAD
  145832. 6022N
  145833. 2/28/96
  145834. VOLODARSKY, L. B.; REZNIKOV, V. A.; OVCHARENKO, V. I.; SYNTHETIC CHEMISTRY OF STABLE NITROXIDES. CRC: BOCA RATON, FL, 1994. A REVIEWa
  145835. GABRIEL WEATHERHEAD
  145836. 6023N
  145837. 2/28/96VbTREDGOLD, R. H.; ORDER IN THIN ORGANIC FILMS. CAMBRIDGE UNIV. PRESS: CAMBRIDGE, UK, 1994. A REVIEWa
  145838. GABRIEL WEATHERHEAD
  145839. 6024N
  145840. 2/28/96V
  145841. ROEGES, N. P. G.; A GUIDE TO THE COMPLETE INTERPRETATION OF INFRARED SPECTRA OF ORGANIC STRUCTURES. WILEY: CHICHESTER, UK. 1994. A REVIEWa
  145842. GABRIEL WEATHERHEAD
  145843. 6025N
  145844. 2/28/96V
  145845. PEREKALIN, V. V.; LIPINA, E. S.; BERESTOVITSKAYA, V. M.; EFREMOV, D. A.; NITROALKENES: CONJUGATED NITRO COMPOUNDS. WILEY: CHICHESTER, UK, 1994. A REVIEWa
  145846. GABRIEL WEATHERHEAD
  145847. 6026N
  145848. 2/28/96VwPATAI, S.; ED.; THE CHEMISTRY OF ORGANIC ARSENIC, ANTIMONY AND BISMUTH COMPOUNDS. WILEY: CHICHESTER, UK, 1994. A REVIEWa
  145849. GABRIEL WEATHERHEAD
  145850. 6027N
  145851. 2/28/96
  145852. MINKIN, V. I.; GLUKHOVTSEV, M. N.; SIMKIN, B. Y.; AROMATICITY AND ANTI AROMATICITY: ELECTRONIC AND STRUCTURAL ASPECTS. WILEY: NEW YORK, N.Y., 1994. A REVIEWa
  145853. GABRIEL WEATHERHEAD
  145854. 6028N
  145855. 2/28/96V
  145856. LEE, Y. C.; LEE, R. T.; EDS.; NEOGLYCOCONJUGATES: PREPARATION AND APPLICATIONS.   ACADEMIC: SAN DIEGO, CALIFORNIA, 1994. A REVIEWa
  145857. GABRIEL WEATHERHEAD
  145858. 6029N
  145859. 2/28/96V
  145860. FRIED, B.; SHERMA, J.; THIN
  145861. LAYER CHROMATOGRAPHY: TECHNIQUES AND APPLICATIONS, THIRD EDITION, REVISED AND EXPANDED. (CHROMATO GRAPHIC SCIENCE SERIES, VOL. 66). DEKKER: NEW YORK, N.Y, 1994. A REVIEWa
  145862. GABRIEL WEATHERHEAD
  145863. 6030N
  145864. 2/28/96V
  145865. CYVIN, S. J.; BRUNVOLL, J.; CHEN, R. S.; CYVIN, B. N.; ZHANG, F. J.; THEORY OF CORONOID HYDROCARBONS II. (LECTURE NOTES CHEMISTRY, VOL. 62).  SPRINGER: BERLIN, GERMANY. 1994. A REVIEWa
  145866. GABRIEL WEATHERHEAD
  145867. 6031N
  145868. 2/28/96
  145869. CHENG, W.
  145870. H.; KUNG, H. H.; EDS.; METHANOL PRODUCTION AND USE. (CHEMISTRY AND INDUSTRY, VOL. 57).  DEKKER: NEW YORK, NY, 1994. A REVIEWa
  145871. GABRIEL WEATHERHEAD
  145872. 6032N
  145873. 2/28/96VyBATESON, J. H.; MITCHELL, M. B.; EDS.; ORGANOMETALLIC REAGENTS IN ORGANIC SYNTHESIS. ACADEMIC: LONDON, UK, 1994. A REVIEWa
  145874. GABRIEL WEATHERHEAD
  145875. 6033N
  145876. 2/28/96V
  145877. BASAVA, C.; ANANTHARAMAIAH, G. M.; EDS.; PEPTIDES: DESIGN, SYNTHESIS AND BIOLOGICAL ACTIVITY.  BIRKHAEUSER: BOSTON, MA. 1994. A REVIEWa
  145878. GABRIEL WEATHERHEAD
  145879. 6034N
  145880. 2/28/96V
  145881. RAHMAN; ED.; STEREOSELECTIVE SYNTHESIS (PART I). (STUDIES IN NATURAL PRODUCT CHEMISTRY, VOL. 14). ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145882. GABRIEL WEATHERHEAD
  145883. 6035N
  145884. 2/28/96
  145885. CONNOLLY, J. D.; HILL, R. A.; TRITERPENOIDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145886. GABRIEL WEATHERHEAD
  145887. 6036N
  145888. 2/28/96V
  145889. MAHATO, S. B.; GLYCOSIDES, SAPONINS AND SAPOGENINS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145890. GABRIEL WEATHERHEAD
  145891. 6037N
  145892. 2/28/96V
  145893. ZEELEN, F. J.; STEROIDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145894. GABRIEL WEATHERHEAD
  145895. 6038N
  145896. 2/28/96
  145897. HANSON, J. R.; DITERPENOIDS AND SESTERTERPENOIDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145898. GABRIEL WEATHERHEAD
  145899. 6039N
  145900. 2/28/96V
  145901. HEWESON, A. T.; THE SESQUITERPENOIDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145902. GABRIEL WEATHERHEAD
  145903. 6040N
  145904. 2/28/96V
  145905. LIVINGSTONE, R.; BICARBOCYCLIC NATURAL PRODUCTS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145906. GABRIEL WEATHERHEAD
  145907. 6041N
  145908. 2/28/96
  145909. MARCHAND, A. P.; POLYCARBOCYCLIC BRIDGED RING COMPOUNDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145910. GABRIEL WEATHERHEAD
  145911. 6042N
  145912. 2/28/96V
  145913. SAINSBURY, M.; POLYCYCLIC COMPOUNDS. FUSED OR CONDENSED CYCLIC SYSTEMS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145914. GABRIEL WEATHERHEAD
  145915. 6043N
  145916. 2/28/96
  145917. WILLS, M.; POLYCARBOCYCLIC COMPOUNDS WITH SEPARATE RING SYSTEMS, AND SPIRO COMPOUNDS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEW
  145918. GABRIEL WEATHERHEAD
  145919. 6044N
  145920. 2/28/96
  145921. EWING, D. F.; LARGE ALICYCLIC RING SYSTEMS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145922. GABRIEL WEATHERHEAD
  145923. 6045N
  145924. 2/28/96V
  145925. EWING, D. F.; THE CYCLOHEPTANES AND CYCLOOCTANES.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145926. GABRIEL WEATHERHEAD
  145927. 6046N
  145928. 2/28/96V
  145929. PEARSON, A. J.; CYCLOHEXADIENES  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145930. GABRIEL WEATHERHEAD
  145931. 6047N
  145932. 2/28/96
  145933. GRIBBLE, G. W.; NATURAL PRODUCTS CONTAINING A CYCLOHEXANE, CYCLO HEXENE, OR CYCLOHEXADIENE SUBUNIT.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEW
  145934. GABRIEL WEATHERHEAD
  145935. 6048N
  145936. 2/28/96V
  145937. BOLTON, R.; CYCLOHEXANE AND ITS DERIVATIVES  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145938. GABRIEL WEATHERHEAD
  145939. 6049N
  145940. 2/28/96V
  145941. EWING, D. F.; CYCLOPENTADIENE.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145942. GABRIEL WEATHERHEAD
  145943. 6050N
  145944. 2/28/96
  145945. %TAYLOR, R. J. K.; PYKE, S. G.; PYKE, S. M.; NATURAL PRODUCTS CONTAINING THE CYCLOPENTANE SUB
  145946. UNIT: PROSTAGLANDINS.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEW
  145947. GABRIEL WEATHERHEAD
  145948. 6051N
  145949. 2/28/96V
  145950. HURST, D. T.; THE CYCLOPENTANES.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145951. GABRIEL WEATHERHEAD
  145952. 6052N
  145953. 2/28/96V
  145954. HURST, D. T.; THE CYCLOBUTANES.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145955. GABRIEL WEATHERHEAD
  145956. 6053N
  145957. 2/28/96
  145958. WONG, H. N. C.; THE CYCLOPROPANES.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COMPOUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEWa
  145959. GABRIEL WEATHERHEAD
  145960. 6054N
  145961. 2/28/96
  145962. CRABB, T. A.; PATEL, A.V.; ALICYCLIC HYDROCARBONS, CONFORMATION AND STEREOCHEMISTRY.  SECOND SUPPLEMENTS TO THE 2ND EDITION OF RODD'S CHEMISTRY OF CARBON COMPOUNDS, VOL. 2. ALICYCLIC COM POUNDS.  SAINSBURY, M.;  ED. ELSEVIER: AMSTERDAM, NETHERLANDS, 1994. A REVIEW
  145963. GABRIEL WEATHERHEAD
  145964. 6055N
  145965. 2/28/96VVSTECKHAN, E.; ELECTROENZYMATIC SYNTHESIS.  TOP. CUR. CHEM. 1994, 170, 83
  145966. 111. A REVIEWa
  145967. GABRIEL WEATHERHEAD
  145968. 6056N
  145969. 2/28/96VoFUCHIGAMI, T.; ELECTROCHEMICAL REACTIONS OF FLUOROORGANIC COMPOUNDS.  TOP. CUR. CHEM. 1994, 170, 1
  145970. 37. A REVIEWa
  145971. GABRIEL WEATHERHEAD
  145972. 6057N
  145973. 2/28/96
  145974. SCOTT, A. I.; THE DISCOVERY OF NATURE'S PATHWAY TO VITAMIN B12, A 25 YEAR ODYSSEY. TETRAHEDRON 1994, 50(47), 13315
  145975. 33. A REVIEWa
  145976. GABRIEL WEATHERHEAD
  145977. 6058N
  145978. 2/28/96V
  145979. MIDDLEMISS, D.; WATSON, S. P.; A MEDICINAL CHEMISTRY CASE STUDY: AN ACCOUNT OF AN ANGIOTENSIN II ANTAGONIST DRUG DISCOVERY PROGRAM. TETRAHEDRON 1994, 50(46), 13049
  145980. 80. A REVIEWa
  145981. GABRIEL WEATHERHEAD
  145982. 6059N
  145983. 2/28/96VgMORIN, C.; THE CHEMISTRY OF BORON ANALOGS OF BIOMOLECULES. TETRAHEDRON 1994, 50(44), 12521
  145984. 69. A REVIEWa
  145985. GABRIEL WEATHERHEAD
  145986. 6060N
  145987. 2/28/96V
  145988. AGROFOGLIO, L.; SUHAS, E.; FARESE, A.; CONDOM, R.; CHALLAND, S. R.; EARL, R. A.; GUEDJ, R.; SYNTHESIS OF CARBOCYCLIC NUCLEOSIDES. TETRAHEDRON 1994, 50(36), 10611
  145989. 70. A REVIEWa
  145990. GABRIEL WEATHERHEAD
  145991. 6061N
  145992. 2/28/96V
  145993. ANT, J.
  145994. M.; MECHANISMS AND REACTIVITY IN ELECTRON TRANSFER INDUCED AROMATIC NUCLEOPHILIC SUBSTITUTION. RECENT ADVANCES. TETRAHEDRON 1994, 50(34), 10117
  145995. 65. A REVIEW
  145996. GABRIEL WEATHERHEAD
  145997. 6062N
  145998. 2/28/96VyCOLE, D. C.; RECENT STEREOSELECTIVE SYNTHETIC APPROACHES TO BETA
  145999. AMINO ACIDS. TETRAHEDRON 1994, 50(32), 9517
  146000. 82. A REVIEWa
  146001. GABRIEL WEATHERHEAD
  146002. 6063N
  146003. 2/28/96V}BESSE, P.; VESCHAMBRE, H.; CHEMICAL AND BIOLOGICAL SYNTHESIS OF CHIRAL EPOXIDES. TETRAHEDRON 1994, 50(30), 8885
  146004. 927. A REVIEWa
  146005. GABRIEL WEATHERHEAD
  146006. 6064N
  146007. 2/28/96V
  146008. O'DONNELL, M. J.; WU, S. D.; HUFFMAN, J. C.; A NEW ACTIVE CATALYST SPECIES FOR ENANTIOSELECTIVE ALKYLATION BY PHASE
  146009. TRANSFER CATALYSIS. TETRAHEDRON 1994, 50(15), 4507
  146010. 18. A REVIEWa
  146011. GABRIEL WEATHERHEAD
  146012. 6065N
  146013. 2/28/96VxLUBINEAU, A.; AUG
  146014. , J.; QUENEAU, Y.; WATER
  146015. PROMOTED ORGANIC REACTIONS.  SYNTHESIS
  146016. STUTTGART 1994, (8),  741
  146017. 60. A REVIEWa
  146018. GABRIEL WEATHERHEAD
  146019. 6066N
  146020. 2/28/96
  146021. LEY, S. V.; NORMAN, J.; GRIFFITH, W. P.; MARSDEN, S. P.; TETRAPROPYL AMMONIUM PERRUTHENATE, PR4N+RUO4
  146022. , TPAP: A CATALYTIC OXIDANT FOR ORGANIC SYNTHESIS.  SYNTHESIS
  146023. STUTTGART 1994, (7), 639
  146024. 66. A REVIEWa
  146025. GABRIEL WEATHERHEAD
  146026. 6067N
  146027. 2/28/96VgWALDMANN, H.; ASYMMETRIC HETERO
  146028. DIELS
  146029. ALDER REACTIONS. SYNTHESIS
  146030.  STUTTGART 1994, (6), 535
  146031. 51. A REVIEWa
  146032. GABRIEL WEATHERHEAD
  146033. 6068N
  146034. 2/28/96V
  146035. BOIADJIEV, S. E.; LIGHTNER, D. A.; SYNTHETIC STRATEGIES FOR UNDER STANDING BILIRUBIN STEREOCHEMISTRY. SYNLETT 1994, (10), 777
  146036. 85. A REVIEWa
  146037. GABRIEL WEATHERHEAD
  146038. 6069N
  146039. 2/28/96V
  146040. LEE, W. Y.; THE CHEMISTRY OF {1N} ORTHOCYCLOPHANES 
  146041.  NEW CLASSES OF IONOPHORES, STARANDS AND KETONANDS. SYNLETT 1994, (10), 765
  146042. 76. A REVIEWa
  146043. GABRIEL WEATHERHEAD
  146044. 6070N
  146045. 2/28/96V
  146046. KOBAYASHI, S.; RARE EARTH METAL TRIFLUOROMETHANESULFONATES AS WATER
  146047. TOLERANT LEWIS ACID CATALYSTS IN ORGANIC SYNTHESIS. SYNLETT 1994, (9), 689
  146048. 701. A REVIEW
  146049. GABRIEL WEATHERHEAD
  146050. 6071N
  146051. 2/28/96VRMOODY, C. J.; SYNTHESIS OF CARBAZOLE ALKALOIDS. SYNLETT 1994, (9), 681
  146052. 8. A REVIEWa
  146053. GABRIEL WEATHERHEAD
  146054. 6072N
  146055. 2/28/96V}BURGESS, K.; HO, K.
  146056. K.; MOYE
  146057. SHERMAN, D.; ASYMMETRIC SYNTHESES OF 2,3
  146058. METHANOAMINO ACIDS. SYNLETT 1994, (8), 575
  146059. 83. A REVIEWa
  146060. GABRIEL WEATHERHEAD
  146061. 6073N
  146062. 2/28/96V
  146063. FARINA,V.; KANT, J.; THE DEVELOPMENT OF ORGANOMETALLIC METHOD OLOGIES FOR THE STEREOSPECIFIC INTRODUCTION OF CEPHALOSPORIN SIDE CHAINS. SYNLETT 1994, (8), 565
  146064. 74. A REVIEWa
  146065. GABRIEL WEATHERHEAD
  146066. 6074N
  146067. 2/28/96V
  146068. LIEBSCHER, J.; G
  146069. AMINOALKYLHETEROCYCLES 
  146070.  ACTUAL ASPECTS OF THE CHEMISTRY OF HISTAMINE ANALOGS. SYNLETT 1994, (7), 471
  146071. 8. A REVIEWa
  146072. GABRIEL WEATHERHEAD
  146073. 6075N
  146074. 2/28/96
  146075. CAMPORA, J.; PANEQUE, M.; POVEDA, M. L.; CARMONA, E.; ORGANONICKEL CHEMISTRY IN ORGANIC SYNTHESIS. SOME APPLICATIONS OF ALKYL AND METALLACYCLIC DERIVATIVES. SYNLETT 1994, (7), 465
  146076. 70. A REVIEWa
  146077. GABRIEL WEATHERHEAD
  146078. 6076N
  146079. 2/28/96V
  146080. FANG, J. M.; WONG, C. H.; ENZYMES IN ORGANIC SYNTHESIS: ALTERATION OF REVERSABLE REACTIONS TO IRREVERSIBLE PROCESSES. SYNLETT 1994, (6), 393
  146081. 402. A REVIEWa
  146082. GABRIEL WEATHERHEAD
  146083. 6077N
  146084. 2/28/96V
  146085. BELSHAW, P. J.; MEYER, S. D.; JOHNSON, D. D.; ROMO, D.; IKEDA, Y.; ANDRUS, M.; ALBERG, D. G.; SCHULTZ, L. W.; CLARDY, J.; SCHREIBER, S. L.; SYNTHESIS, STRUCTURE AND MECHANISM IN IMMUNOPHILIN RESEARCH. SYNLETT 1994, (6), 381
  146086. 92. A REVIEWa
  146087. GABRIEL WEATHERHEAD
  146088. 6078N
  146089. 2/28/96V
  146090. MONNERET, C.; FLORENT, J.
  146091. C.; ISOSACCHARINO
  146092.  AND GLUCOSACCHARINO
  146093.  LACTONES AS CHIRONS FOR THE SYNTHESES OF NATURAL COMPOUNDS AND ANALOGS OF BIOLOGICAL RELEVANCE. SYNLETT 1994, (5), 305
  146094. 18. A REVIEWa
  146095. GABRIEL WEATHERHEAD
  146096. 6079N
  146097. 2/28/96V
  146098. PRAKASH, O.; SAINI, N.; SHARMA, P. K.; HYPERVALENT IODINE REAGENTS IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS.  SYNLETT 1994, (4), 221
  146099. 7. A REVIEWa
  146100. GABRIEL WEATHERHEAD
  146101. 6080N
  146102. 2/28/96V
  146103. HARADA, T.; OKU, A.; ENANTIODIFFERENTIATING TRANSFORMATION OF PROCHIRAL POLYOLS BY USING MENTHONE AS CHIRAL TEMPLATE. SYNLETT 1994, (2), 95
  146104. 104. A REVIEWa
  146105. GABRIEL WEATHERHEAD
  146106. 6081N
  146107. 2/28/96VqNEDOLYA, N. A.; TROFIMOV, B. A. SULFUR DERIVATIVES OF VINYL ETHERS.  SULFUR REPORTS 1994, 15(3), 339
  146108. 80. A REVIEWa
  146109. GABRIEL WEATHERHEAD
  146110. 6082N
  146111. 2/28/96V
  146112. MCKINNON, D. M.; SOME INVESTIGATIONS ON BRIDGED AND POTENTIALLY BRIDGED ISOTHIAZOLES.  SULFUR REPORTS 1994, 15(2), 317
  146113. 34. A REVIEWa
  146114. GABRIEL WEATHERHEAD
  146115. 6083N
  146116. 2/28/96VoNEDOLYA, N. A.; TROFIMOV, B. A.; SULFUR
  146117. CONTAINING VINYL ETHERS.  SULFUR REPORTS 1994, 15(2), 237
  146118. 316. A REVIEWa
  146119. GABRIEL WEATHERHEAD
  146120. 6084N
  146121. 2/28/96
  146122. HVzBATTERSBY, A. R.; HOW NATURE BUILDS THE PIGMENTS OF LIFE: THE CONQUEST OF VITAMIN B12.  SCIENCE1994, 264, 1551
  146123. 7. A REVIEWa
  146124. GABRIEL WEATHERHEAD
  146125. 6085N
  146126. 2/28/96V
  146127. ZELLER, K.
  146128. P.; MEWES, K.; EHNINGER, G.; BLANZ, J.; FORMATION OF REACTIVE INTERMEDIATES BY CYTOCHROME P
  146129. 450 MEDIATED OXIDATION OF THE ANTI
  146130. CANCER DRUG MITOXANTRONE.  PURE APPL. CHEM. 1994, 66(10/11), 2415
  146131. 18. A REVIEWa
  146132. GABRIEL WEATHERHEAD
  146133. 6086N
  146134. 2/28/96VkPFANDER,  H.;  C
  146135. CAROTENOIDS AND  C
  146136. CAROTENOIDS.  PURE APPL. CHEM. 1994, 66(10/11), 2369
  146137. 74. A REVIEWa
  146138. GABRIEL WEATHERHEAD
  146139. 6087N
  146140. 2/28/96V
  146141. PARIZA, R. J.; FREIBERG, L. A.; ERYTHROMYCIN: NEW CHEMISTRY ON AN OLD COMPOUND.  PURE APPL. CHEM. 1994, 66(10/11), 2365
  146142. 8. A REVIEWa
  146143. GABRIEL WEATHERHEAD
  146144. 6088N
  146145. 2/28/96V
  146146. MAHIDOL, C.; SAHAKITPICHAN, P.; RUCHIRAWAT, S.; BIOACTIVE NATURAL PRODUCTS FROM THAI PLANTS.  PURE APPL. CHEM. 1994, 66(10/11), 2353
  146147. 6. A REVIEWa
  146148. GABRIEL WEATHERHEAD
  146149. 6089N
  146150. 2/28/96V
  146151. GUIDI, A.; CANFARINI, F.; GIOLITTI, A.; PASQUI, F.; PESTELLINI, V.; ARCAMONE, F.; SYNTHESIS OF NEW ANTITUMOR ANTHRACYCLINES: DERIVATIVES BEARING A FLUORINE SUBSTITUTION AT POSITION 8 OR 10.  PURE APPL. CHEM. 1994, 66(10/11), 2319
  146152. 22. A REVIEWa
  146153. GABRIEL WEATHERHEAD
  146154. 6090N
  146155. 2/28/96
  146156. APSIMON, J. W.; BLACKWELL, B. A.; EDWARDS, O. E.; FRUCHIER, A.; MILLER, J. D.; SAVARD, M.; YOUNG J. C.; THE CHEMISTRY OF FUMONISINS AND RELATED COMPOUNDS. FUMONISINS FROM FUSARIUM MONILIFORME: CHEMISTRY, STRUCTURE AND BIOSYNTHESIS.  PURE APPL. CHEM. 1994, 66(10/11), 2315
  146157. 18. A REVIEW
  146158. GABRIEL WEATHERHEAD
  146159. 6091N
  146160. 2/28/96V
  146161. SENER, B.; RECENT RESULTS IN THE SEARCH FOR BIOACTIVE COMPOUNDS FROM TURKISH MEDICINAL
  146162. PLANTS.  PURE APPL. CHEM. 1994, 66(10/11), 2295
  146163. 8. A REVIEWa
  146164. GABRIEL WEATHERHEAD
  146165. 6092N
  146166. 2/28/96
  146167. CORDELL, G. A.; ANGERHOFER, C. K.; PEZZUTO, J. M.; RECENT STUDIES ON CYTOTOXIC, ANTI
  146168. HIV AND ANTIMALARIAL AGENTS FROM PLANTS.  PURE APPL. CHEM. 1994, 66(10/11), 2283
  146169. 6. A REVIEWa
  146170. GABRIEL WEATHERHEAD
  146171. 6093N
  146172. 2/28/96VwNISHIBE, S.; BIOACTIVE PHENOLIC COMPOUNDS IN TRADITIONAL MEDICINES. PURE APPL. CHEM.  1994, 66(10/11), 2263
  146173. 6. A REVIEWa
  146174. GABRIEL WEATHERHEAD
  146175. 6094N
  146176. 2/28/96V
  146177. NAKATANI, K.; FUKUDA,Y.; TERASHIMA, S.; SYNTHESIS AND CYTOTOXICITY OF NATURAL (+)
  146178. DUOCARMYCIN A AND ITS THREE POSSIBLE STEREOISOMERS.  PURE APPL. CHEM. 1994, 66(10/11), 2255
  146179. 8. A REVIEWa
  146180. GABRIEL WEATHERHEAD
  146181. 6095N
  146182. 2/28/96VqKAMERLING, J. P.; STRUCTURAL STUDIES ON GLYCOPROTEIN GLYCANS.  PURE APPL. CHEM. 1994, 66(10/11), 2235
  146183. 8. A REVIEWa
  146184. GABRIEL WEATHERHEAD
  146185. 6096N
  146186. 2/28/96
  146187. BLOCK, E.; DEORAZIO, R.; CHEMISTRY IN A SALAD BOWL: COMPARATIVE ORGANOSULFUR CHEMISTRY OF GARLIC, ONION AND SHIITAKE MUSHROOMS.  PURE APPL. CHEM. 1994, 66(10/11), 2205
  146188. 6. A REVIEWa
  146189. GABRIEL WEATHERHEAD
  146190. 6097N
  146191. 2/28/96V
  146192. OGASAWARA, K.; ENANTIOCONTROLLED ROUTE TO NATURAL PRODUCTS USING CHIRAL EQUIVALENTS OF CYCLOPENTENONE AND CYCLOHEXENONE.  PURE APPL. CHEM. 1994, 66(10/11), 2119
  146193. 22 (ENGLISH). A REVIEWa
  146194. GABRIEL WEATHERHEAD
  146195. 6098N
  146196. 2/28/96V
  146197. WITCZAK, Z. J.; SYNTHESIS OF C
  146198. GLYCOSYL COMPOUNDS AND OTHER NATURAL PRODUCTS FROM LEVOGLUCOSENONE.  PURE APPL. CHEM. 1994, 66(10/11), 2189
  146199. 92. A REVIEWa
  146200. GABRIEL WEATHERHEAD
  146201. 6099N
  146202. 2/28/96VpSUZUKI, K.; TOTAL SYNTHESIS OF ARYL C
  146203. GLYCOSIDE ANTIBIOTICS.  PURE APPL. CHEM. 1994, 66(10/11), 2175
  146204. 8. A REVIEWa
  146205. GABRIEL WEATHERHEAD
  146206. 6100N
  146207. 2/28/96
  146208. SOLLADIE, G.; ANTONIO, A.; CARMEN D.; ASYMMETRIC SYNTHESIS OF NATURAL PRODUCTS MONITORED BY CHIRAL SULFOXIDES.  PURE APPL. CHEM. 1994, 66(10/11), 2159
  146209. 62. A REVIEWa
  146210. GABRIEL WEATHERHEAD
  146211. 6101N
  146212. 2/28/96V
  146213. SNIECKUS, V.; COMBINED DIRECTED ORTHO METALATION
  146214. CROSS COUPLING STRATEGIES. DESIGN FOR NATURAL PRODUCT SYNTHESIS.  PURE APPL. CHEM. 1994, 66(10/11), 2155
  146215. 8. A REVIEWa
  146216. GABRIEL WEATHERHEAD
  146217. 6102N
  146218. 2/28/96V
  146219. SHIOIRI, T.; MATSUURA, F.; HAMADA, Y.; USE OF THE ARYL GROUPS AS THE CARBOXYL SYNTHON. APPLICATION TO THE SYNTHESIS OF SOME NATURAL PRODUCTS CONTAINING HYDROXY AMINO ACID FUNCTIONS.  PURE APPL. CHEM. 1994, 66(10/11), 2151
  146220. 4. A REVIEWa
  146221. GABRIEL WEATHERHEAD
  146222. 6103N
  146223. 2/28/96V
  146224. PARKER, K. A.; NOVEL METHODS FOR THE SYNTHESIS OF C
  146225. ARYL GLYCOSIDE NATURAL PRODUCTS.  PURE APPL. CHEM. 1994, 66(10/11), 2135
  146226. 8. A REVIEWa
  146227. GABRIEL WEATHERHEAD
  146228. 6104N
  146229. 2/28/96
  146230. MIYATA, O.; NAITO, T.; NINOMIYA, I.; STEREOSPECIFIC ADDITION OF THIO PHENOL TO ELECTRON
  146231. DEFICIENT DOUBLE BOND AND ITS APPLICATION TO NATURAL PRODUCT SYNTHESIS. 1994, 66(10/11), 2115
  146232. 18. A REVIEWa
  146233. GABRIEL WEATHERHEAD
  146234. 6105N
  146235. 2/28/96V
  146236. MOODY, C. J.; DOYLE, K. J.; ELLIOTT, M. C.; MOWLEM, T. J.; SYNTHESIS OF HETEROCYCLIC NATURAL PRODUCTS: MODEL STUDIES TOWARDS DIAZONAMIDE A.  PURE APPL. CHEM. 1994, 66(10/11), 2107
  146237. 10. A REVIEWa
  146238. GABRIEL WEATHERHEAD
  146239. 6106N
  146240. 2/28/96V
  146241. LEY, S. V.; SYNTHESIS AND CHEMISTRY OF THE INSECT ANTIFEEDANT AZADIRACHTIN.  PURE APPL. CHEM. 1994, 66(10/11), 2099
  146242. 102. A REVIEWa
  146243. GABRIEL WEATHERHEAD
  146244. 6107N
  146245. 2/28/96V
  146246. KROTO, H. W.; TAYLOR, R.; WALTON, D. R. M.; THE STRUCTURE AND REACTIVITY OF C60.  PURE APPL. CHEM. 1994, 66(10/11), 2091
  146247. 4. A REVIEWa
  146248. GABRIEL WEATHERHEAD
  146249. 6108N
  146250. 2/28/96
  146251. KOZIKOWSKI, A. P.; MA, D.; DU, L.; LEWIN, N. E.; BLUMBERG, P. M.; A PALLADIUM CATALYZED ROUTE TO A BENZOFURAN ANALOG OF INDOLACTAM V (ILV): EFFECTS ON PKC ISOTYPE SELECTIVITY.  PURE APPL. CHEM. 1994, 66(10/11), 2087
  146252. 90. A REVIEWa
  146253. GABRIEL WEATHERHEAD
  146254. 6109N
  146255. 2/28/96V
  146256. KITAHARA, T.; KINOSHITA, Y.; AONO, S.; MIYAKE, M.; HASEGAWA, T.; WATANABE, H.; MORI, K.; SYNTHETIC STUDIES ON PHENAZINE ANTIBIOTICS AND ANTHERIDIC ACID.  PURE APPL. CHEM. 1994, 66(10/11), 2083
  146257. 6. A REVIEWa
  146258. GABRIEL WEATHERHEAD
  146259. 6110N
  146260. 2/28/96V
  146261. JEFFORD, C. W.; LU, Z.; WANG, J. B.; CONCISE ENANTIOSPECIFIC SYNTHESES OF A
  146262. HYDROXY
  146263. AMINO ACIDS AND INDOLIZIDINES OF NATURAL ORIGIN.  PURE APPL. CHEM. 1994, 66(10/11), 2075
  146264. 8. A REVIEWa
  146265. GABRIEL WEATHERHEAD
  146266. 6111N
  146267. 2/28/96V
  146268. HUDLICKY, T.; ENANTIOSELECTIVE SYNTHESIS OF ALKALOIDS AND CARBO HYDRATES VIA CHEMOENZYMIC METHODS.  PURE APPL. CHEM. 1994, 66(10/11), 2067
  146269. 70. A REVIEWa
  146270. GABRIEL WEATHERHEAD
  146271. 6112N
  146272. 2/28/96
  146273. +HELQUIST, P.; BERGDAHL, M.; HETT, R.; GANGLOFF, A. R.; DEMILLEQUAND, M.; COTTARD, M.; MADER, M. M.; FRIEBE, T.; IQBAL, J.; WU, Y.; 
  146274. KERMARK, B.; REIN, T.; KANN, N.; SYNTHESIS OF MACROCYCLIC LACTAM/LACTONE DERIVATIVES HAVING ANTIMICROBIAL ACTIVITY.  PURE APPL. CHEM. 1994, 66(10/11), 2063
  146275. 6. A REVIEW
  146276. GABRIEL WEATHERHEAD
  146277. 6113N
  146278. 2/28/96
  146279. DE GROOT, A.; JANSEN, B. J. M.; VERSTEGEN
  146280. HAAKSMA, A. A.; SWARTS, H. J.; ORRU, R. V. A.; STORK, G. A.; WIJNBERG, J. B. P. A.; RECENT DEVELOPMENTS IN THE SYNTHESIS OF DRIMANE AND LACTARANE SESQUITERPENES.  PURE APPL. CHEM. 1994,  66(10/11), 2053
  146281. 6. A REVIEW
  146282. GABRIEL WEATHERHEAD
  146283. 6114N
  146284. 2/28/96V
  146285. AHMAR, M.; DUYCK, C.; FLEMING, I.; STEREOCONTROL USING SILICON: A SYNTHESIS OF METHYL (+)
  146286. NONACTATE.  PURE APPL. CHEM. 1994, 66(10/11), 2049
  146287. 52. A REVIEWa
  146288. GABRIEL WEATHERHEAD
  146289. 6115N
  146290. 2/28/96
  146291. BRUNNER, H.; NATURAL PRODUCTS BY ENANTIOSELECTIVE CATALYSIS WITH TRANSITION METAL COMPOUNDS.  PURE APPL. CHEM. 1994, 66(10/11), 2033
  146292. 6. A REVIEWa
  146293. GABRIEL WEATHERHEAD
  146294. 6116N
  146295. 2/28/96V
  146296. ATEEQ, H. S.; HIGHER
  146297. ORDER CYCLOADDITION REACTIONS IN NATURAL PRODUCT SYNTHESIS.  PURE APPL. CHEM. 1994, 66(10/11), 2029
  146298. 32. A REVIEWa
  146299. GABRIEL WEATHERHEAD
  146300. 6117N
  146301. 2/28/96VqZENK, M. H.; THE FORMATION OF BENZOPHENANTHRIDINE ALKALOIDS.  PURE APPL. CHEM. 1994,  66(10/11), 2023
  146302. 8. A REVIEWa
  146303. GABRIEL WEATHERHEAD
  146304. 6118N
  146305. 2/28/96V
  146306. VOELTER, W.; STOEVA, S.; KAISER, T.; GRUBLER, G.; MIHELIC, M.; ECHNER, H.; HARITOS, A. A.; SEEGER, H.; LIPPERT, T. H. DESIGN AND DEVELOPMENT OF SYNTHETIC PEPTIDE ANTIGENS.  PURE APPL. CHEM. 1994, 66(10/11), 2015
  146307. 22. A REVIEWa
  146308. GABRIEL WEATHERHEAD
  146309. 6119N
  146310. 2/28/96
  146311. TROST, B. M.; ENHANCED SYNTHETIC EFFICIENCY TOWARDS NATURAL PRODUCTS VIA TRANSITION METAL CATALYZED REACTIONS.  PURE APPL. CHEM. 1994, 66(10/11), 2007
  146312. 14. A REVIEWa
  146313. GABRIEL WEATHERHEAD
  146314. 6120N
  146315. 2/28/96VzMORI, K.; SYNTHETIC AND STEREOCHEMICAL ASPECTS OF PHEROMONE CHEMISTRY.  PURE APPL. CHEM. 1994, 66(10/11), 1991
  146316. 8. A REVIEWa
  146317. GABRIEL WEATHERHEAD
  146318. 6121N
  146319. 2/28/96V
  146320. RAHMAN; CHOUDHARY, M. I.; RECENT DISCOVERIES IN THE CHEMISTRY OF NATURAL PRODUCTS.  PURE APPL. CHEM. 1994, 66(10/11), 1967
  146321. 74. A REVIEWa
  146322. GABRIEL WEATHERHEAD
  146323. 6122N
  146324. 2/28/96V
  146325. LEHN, J.
  146326. M.; PERSPECTIVES IN SUPRAMOLECULAR CHEMISTRY: FROM MOLECULAR RECOGNITION TOWARDS SELF
  146327. ORGANIZATION.  PURE APPL. CHEM. 1994, 66(10/11), 1961
  146328. 6. A REVIEWa
  146329. GABRIEL WEATHERHEAD
  146330. 6123N
  146331. 2/28/96V
  146332. BARTON, D. H. R.; THE INVENTION OF CHEMICAL REACTIONS OF RELEVANCE TO THE CHEMISTRY OF NATURAL PRODUCTS.  PURE APPL. CHEM. 1994, 66(10/11), 1943
  146333. 54. A REVIEW
  146334. GABRIEL WEATHERHEAD
  146335. 6124N
  146336. 2/28/96V
  146337. PEIJNENBURG, W. J. G. M.; STRUCTURE
  146338. ACTIVITY
  146339. RELATIONSHIPS FOR BIODEGRADATION 
  146340.  A CRITICAL REVIEW.  PURE APPL. CHEM. 1994, 66(9), 1931
  146341. 41. A REVIEWa
  146342. GABRIEL WEATHERHEAD
  146343. 6125N
  146344. 2/28/96
  146345. JIANG, X. K.; NEW CONCEPTS FOR STUDYING AND UNDERSTANDING THE AGGREGATION, COAGGREGATION, DE
  146346. AGGREGATION AND SELF
  146347. COILING OF ORGANIC MOLECULES 
  146348.  WHY ARE CHOLESTEROLS AND TRIGLYCERIDES CULPRITS OF ARTERIOSCLEROSIS.  PURE APPL. CHEM. 1994, 66(8),1621
  146349. 8. A REVIEW
  146350. GABRIEL WEATHERHEAD
  146351. 6126N
  146352. 2/28/96V
  146353. ERNST, R. R.; RECENT DEVELOPMENT IN NMR METHODOLOGY FOR THE STUDY OF MOLECULAR STRUCTURE AND DYNAMICS.  PURE APPL. CHEM. 1994, 66(8), 1583
  146354. 8. A REVIEWa
  146355. GABRIEL WEATHERHEAD
  146356. 6127N
  146357. 2/28/96V]RICHARDS, W. G.; COMPUTER
  146358. AIDED DRUG DESIGN.  PURE APPL. CHEM. 1994, 66(8), 1589
  146359. 96. A REVIEWa
  146360. GABRIEL WEATHERHEAD
  146361. 6128N
  146362. 2/28/96
  146363. GRIFFITHS, S. L.; MARCOS, C. F.; PERRIO, S.; SABERI, S. P.; THOMAS, S. E.; TUSTIN, G. J.; WIERZCHLEYSKI, A. T.; SULFOXIDES AND STEREOCHEMICAL CONTROL IN ORGANOMETALLIC CHEMISTRY.  PURE APPL. CHEM. 1994, 66(7), 1565
  146364. 72. A REVIEWa
  146365. GABRIEL WEATHERHEAD
  146366. 6129N
  146367. 2/28/96VmSUZUKI, K.; NOVEL LEWIS ACID CATALYSIS IN ORGANIC SYNTHESIS.  PURE APPL. CHEM. 1994, 66(7), 1557
  146368. 64. A REVIEWa
  146369. GABRIEL WEATHERHEAD
  146370. 6130N
  146371. 2/28/96V
  146372. RAJANBABU, T. V.; CASALNUOVO, A. L.; ELECTRONIC EFFECTS IN ASYMMETRIC CATALYSIS: ENANTIOSELECTIVE CARBON
  146373. CARBON BOND
  146374. FORMING PROCESSES.  PURE APPL. CHEM. 1994, 66(7), 1535
  146375. 42. A REVIEWa
  146376. GABRIEL WEATHERHEAD
  146377. 6131N
  146378. 2/28/96V
  146379. MONTANARI, F.; BIOMIMETIC OXYGENATIONS CATALYZED BY METALLO PORPHYRINS AND METALLOPORPHINOIDS BEARING CO
  146380. CATALYTIC FUNCTIONS.  PURE APPL. CHEM. 1994, 66(7), 1519
  146381. 26. A REVIEWa
  146382. GABRIEL WEATHERHEAD
  146383. 6132N
  146384. 2/28/96
  146385. LU, X.; MA, S.; JI, J.; ZHU, G.; JIANG, H.; CONSTRUCTION OF ALPHA
  146386. ALKYLIDENE
  146387.  GAMMA
  146388. BUTYROLACTONES FROM ACYCLIC ESTER PRECURSORS.  PURE APPL. CHEM. 1994, 66(7), 1501
  146389. 8. A REVIEWa
  146390. GABRIEL WEATHERHEAD
  146391. 6133N
  146392. 2/28/96V
  146393. LIPSCHUTZ, B. H.; BHANDARI, A.; LINDSLEY, C.; KEIL, R.; WOOD, M. R.; NEW SYNTHETIC METHODS BASED ON ORGANOZIRCONIUM AND ORGANOCOPPER CHEMISTRY.  PURE APPL. CHEM. 1994, 66(7), 1493
  146394. 500. A REVIEWa
  146395. GABRIEL WEATHERHEAD
  146396. 6134N
  146397. 2/28/96VkKOGA, K.; ASYMMETRIC SYNTHESIS MEDIATED BY CHIRAL LIGANDS.  PURE APPL. CHEM. 1994, 66(7), 1487
  146398. 92. A REVIEWa
  146399. GABRIEL WEATHERHEAD
  146400. 6135N
  146401. 2/28/96
  146402. HOPPE, D.; HINTZE, F.; TEBBEN, P.; PAETOW, M.; AHRENS, H.; SCHWERDTFEGER, J.; SOMMERFELD, P.; HALLER, J.; GUARNIERI, W.; KOLCZEWSKI, S.; HENSE, T.; HOPPE, I.; ENANTIOSELECTIVE SYNTHESIS VIA SPARTEINE
  146403. INDUCED ASYMMETRIC DEPROTONATION.  PURE APPL. CHEM. 1994, 66(7), 1479
  146404. 86. A REVIEW
  146405. GABRIEL WEATHERHEAD
  146406. 6136N
  146407. 2/28/96V
  146408. HIYAMA, T.; HATANAKA, Y.; PALLADIUM
  146409. CATALYZED CROSS
  146410. COUPLING REACTION OF ORGANOMETALLOIDS THROUGH ACTIVATION WITH FLUORIDE ION.  PURE APPL. CHEM. 1994, 66(7), 1471
  146411. 8. A REVIEWa
  146412. GABRIEL WEATHERHEAD
  146413. 6137N
  146414. 2/28/96V
  146415. FALLER, J. W.; MAZZIERI, M. R.; NGUYEN, J. T.; PARR, J.; TOKUNAGA, M.; CONTROLLING STEREOCHEMISTRY IN C
  146416. C AND C
  146417. H BOND FORMATION WITH ELECTRONICALLY ASYMMETRIC ORGANOMETALLICS AND CHIRAL POISONS.  PURE APPL. CHEM. 1994, 66(7), 1463
  146418. 9. A REVIEWa
  146419. GABRIEL WEATHERHEAD
  146420. 6138N
  146421. 2/28/96V
  146422. VAN KOTEN, G.; ASYMMETRIC CATALYSIS WITH CHIRAL ORGANOCOPPER
  146423.  COPPER ARENETHIOLATES.  PURE APPL. CHEM. 1994, 66(7), 1455
  146424. 62. A REVIEWa
  146425. GABRIEL WEATHERHEAD
  146426. 6139N
  146427. 2/28/96V
  146428. SCHROCK, R. R.; RECENT ADVANCES IN THE CHEMISTRY AND APPLICATIONS OF HIGH OXIDATION STATE ALKYLIDENE COMPLEXES.  PURE APPL. CHEM. 1994, 66(7), 1447
  146429. 54. A REVIEWa
  146430. GABRIEL WEATHERHEAD
  146431. 6140N
  146432. 2/28/96
  146433. OVERMAN, L. E.; APPLICATION OF INTRAMOLECULAR HECK REACTIONS FOR FORMING CONGESTED QUATERNARY CARBON CENTERS IN COMPLEX MOLECULE TOTAL SYNTHESIS.  PURE APPL. CHEM. 1994, 66(7), 1423
  146434. 30. A REVIEWa
  146435. GABRIEL WEATHERHEAD
  146436. 6141N
  146437. 2/28/96VtLEY, S. V.; TRICARBONYLIRON LACTONE COMPLEXES IN ORGANIC SYNTHESIS.  PURE APPL. CHEM. 1994, 66(7), 1415
  146438. 22. A REVIEWa
  146439. GABRIEL WEATHERHEAD
  146440. 6142N
  146441. 2/28/96
  146442. AVENT, A. G.; BIRKETT, P. R.; CHRISTIDES, C.; CRANE, J. D.; DARWISH, A. D.; HITCHCOCK, P. B.; KROTO, H. W.; MEIDINE, M. F.; PRASSIDES, K.; TAYLOR, R.; WALTON, D. R. M.; THE FULLERENES 
  146443.  PRECURSORS FOR 21ST CENTURY MATERIALS.  PURE APPL. CHEM. 1994, 66(6), 1389
  146444. 96. A REVIEW
  146445. GABRIEL WEATHERHEAD
  146446. 6143N
  146447. 2/28/96V
  146448. ITO, M.; YAMANO, Y.; SUMIYA, S.; WADA, A.; RECENT PROGRESS IN CAROTENOID AND RETINOID SYNTHESIS.  PURE APPL. CHEM. 1994, 66(5), 939
  146449. 46. A REVIEWa
  146450. GABRIEL WEATHERHEAD
  146451. 6144N
  146452. 2/28/96
  146453. V^MAYER, H.; REFLECTIONS ON CAROTENOID SYNTHESIS.  PURE APPL. CHEM. 1994, 66(5), 931
  146454. 8. A REVIEWa
  146455. GABRIEL WEATHERHEAD
  146456. 6145N
  146457. 2/28/96V
  146458. BOGER, D. L.; DESIGN, SYNTHESIS, AND EVALUATION OF DNA MINOR
  146459. GROOVE BINDING AGENTS 
  146460.  THE DUOCARMYCINS.  PURE APPL. CHEM. 1994, 66(4), 837
  146461. 44. A REVIEWa
  146462. GABRIEL WEATHERHEAD
  146463. 6146N
  146464. 2/28/96V
  146465. KOBAYASHI, M.; KITAGAWA, I.; BIOACTIVE SUBSTANCES ISOLATED FROM MARINE SPONGE. A MINIATURE CONGLOMERATE OF VARIOUS ORGANISMS.  PURE APPL. CHEM. 1994, 66(4), 819
  146466. 26. A REVIEWa
  146467. GABRIEL WEATHERHEAD
  146468. 6147N
  146469. 2/28/96V
  146470. BONAR
  146471. LAW, R. P.; MACKAY, L. G.; WALTER, C. J.; MARVAUD, V.; SANDERS, J. K. M.; TOWARDS SYNTHETIC ENZYMES BASED ON PORPHYRINS AND STEROIDS.  PURE APPL. CHEM. 1994, 66(4), 803
  146472. 10. A REVIEWa
  146473. GABRIEL WEATHERHEAD
  146474. 6148N
  146475. 2/28/96VsPATWARDHAN, S. A; SYNTHESIS OF A, G
  146476. ALKANEDIOLS 
  146477. . A REVIEW.  ORG. PREP. PROCED. INT. 1994, 26(6), 645
  146478. 70. A REVIEWa
  146479. GABRIEL WEATHERHEAD
  146480. 6149N
  146481. 2/28/96V
  146482. BLIZZARD, T. A.; RECENT PROGRESS IN THE SYNTHESIS OF AVERMECTINS AND MILBEMYCINS 
  146483. . A REVIEW.  ORG. PREP. PROCED. INT. 1994, 26(6), 617
  146484. 44. A REVIEWa
  146485. GABRIEL WEATHERHEAD
  146486. 6150N
  146487. 2/28/96V
  146488. WITTENBERGER, S. J.; RECENT DEVELOPMENTS IN TETRAZOLE CHEMISTRY 
  146489. . A REVIEW.  ORG. PREP. PROCED. INT. 1994, 26(5), 499
  146490. 531. A REVIEWa
  146491. GABRIEL WEATHERHEAD
  146492. 6151N
  146493. 2/28/96V
  146494. ELGEMEIE, G. E. H.; ELEZBAWY, S. R.; ALI, H. A.; MANSOUR, A. K.; SYNTHESIS OF SEVERAL N
  146495. SUBSTITUTED AMINO
  146496. PYRIDONES.  ORG. PREP. PROCED. INT. 1994, 26(4), 465
  146497. 8. A REVIEWa
  146498. GABRIEL WEATHERHEAD
  146499. 6152N
  146500. 2/28/96V
  146501. MOTOHASHI, N.; KAWASE, M.; EMRANI, J.; SYNTHESIS OF CARCINOGENIC OXYGENATED DERIVATIVES OF BENZ{C}ACRIDINES 
  146502. . A REVIEW.  ORG. PREP. PROCED. INT. 1994, 26(4), 393
  146503. 420. A REVIEWa
  146504. GABRIEL WEATHERHEAD
  146505. 6153N
  146506. 2/28/96
  146507. BERTRAND, M. P.; RECENT PROGRESS IN THE USE OF SULFONYL RADICALS IN ORGANIC SYNTHESIS 
  146508. . A REVIEW.  ORG. PREP. PROCED. INT. 1994, 26(3), 257
  146509.  90. A REVIEWa
  146510. GABRIEL WEATHERHEAD
  146511. 6154N
  146512. 2/28/96V
  146513. BOUILLON, J. P., ATES, C.; MALIVERNEY, C.; JANOUSEK, Z.; VIEHE, H. G.; B
  146514. TRIFLUOROACETYLATION OF LACTAMS AND BENZOLACTAMS.  ORG. PREP. PROCED. INT. 1994, 26(2), 249
  146515. 55. A REVIEWa
  146516. GABRIEL WEATHERHEAD
  146517. 6155N
  146518. 2/28/96V
  146519. BABU, B. R.; BALASUBRAMANIAM, K. K.; SIMPLE AND FACILE OXIDATION OF ALDEHYDES TO CARBOXYLIC
  146520. ACIDS.  ORG. PREP. PROCED. INT. 1994, 26(1), 123
  146521. 5. A REVIEWa
  146522. GABRIEL WEATHERHEAD
  146523. 6156N
  146524. 2/28/96V
  146525. SANCHEZ, C.; RIBOT, F.; DESIGN OF HYBRID ORGANIC
  146526. INORGANIC MATERIALS SYNTHESIZED VIA SOL
  146527. GEL CHEMISTRY.  NEW J. CHEM. 1994, 18(10), 1007
  146528. 47. A REVIEWa
  146529. GABRIEL WEATHERHEAD
  146530. 6157N
  146531. 2/28/96
  146532. V{OHARE, D.; ORGANIC AND ORGANOMETALLIC GUESTS INTERCALATED IN LAYERED LATTICES.  NEW J. CHEM. 1994. 18(10), 989
  146533. 98. A REVIEWa
  146534. GABRIEL WEATHERHEAD
  146535. 6158N
  146536. 2/28/96V
  146537. DAVE, B. C.; CZERNUSZEWICZ, R. S.; COORDINATION CHEMISTRY OF MANGANESE WITH 2,2'
  146538. BIPYRIDINE 
  146539.  SYNTHETIC ACCESS TO HIGH
  146540. VALENT POLYNUCLEAR OXOMANGANESE COMPLEXES OF BIOLOGICAL RELEVANCE.  NEW J. CHEM. 1994, 18(1), 149
  146541. 55. A REVIEWa
  146542. GABRIEL WEATHERHEAD
  146543. 6159N
  146544. 2/28/96V
  146545. MASUDA, T.; TACHIMORI, H.; DESIGN, SYNTHESIS, AND PROPERTIES OF SUBSTITUTED POLYACETYLENES.  J.  MACRO. SCI.
  146546. PURE  APPL. CHEM. 1994, 31(11), 1675
  146547. 90. A REVIEWa
  146548. GABRIEL WEATHERHEAD
  146549. 6160N
  146550. 2/28/96V
  146551. WANG, T. M.; BRADSHAW, J. S.; IZATT, R. M.; APPLICATIONS OF NMR. SPECTRAL TECHNIQUES FOR THE STUDY OF MACROCYCLE HOST
  146552. ORGANIC GUEST INTERACTIONS 
  146553.  A SHORT REVIEW.  J. HETEROCYCL. CHEM. 1994, 31(5), 1097
  146554. 114. A REVIEWa
  146555. GABRIEL WEATHERHEAD
  146556. 6161N
  146557. 2/28/96
  146558. IDDON, B.; NGOCHINDO, R. I.; SYNTHESIS AND REACTIONS OF LITHIATED MONOCYCLIC AZOLES CONTAINING 2 OR MORE HETERO
  146559. ATOMS. PART 4: IMIDAZOLES.  HETEROCYCLES 1994, 38(11), 2487
  146560. 568. A REVIEWa
  146561. GABRIEL WEATHERHEAD
  146562. 6162N
  146563. 2/28/96V
  146564. VEINBERG, G. A.; LUKEVICS, E.; ORGANOSILICON AND ORGANOTIN COMPOUNDS IN THE SYNTHESIS AND TRANSFORMATION OF B
  146565. LACTAMS.  HETEROCYCLES 1994, 38(10), 2309
  146566. 42. A REVIEWa
  146567. GABRIEL WEATHERHEAD
  146568. 6163N
  146569. 2/28/96V
  146570. YUXIANG, O.; BOREN, C. JIARONG, L. SHUAN, D.; JIANJUN, L. HUIPING, J. SYNTHESIS OF NITRO
  146571. DERIVATIVES OF TRIAZOLES.  HETEROCYCLES 1994, 38(7), 1651
  146572. 64. A REVIEWa
  146573. GABRIEL WEATHERHEAD
  146574. 6164N
  146575. 2/28/96VfTURCK, A.; PL
  146576. , N.; QU
  146577. GUINER, G.; METALATION OF DIAZINES. HETEROCYCLES 1994, 37(3), 2149
  146578. 72. A REVIEWa
  146579. GABRIEL WEATHERHEAD
  146580. 6165N
  146581. 2/28/96
  146582. GRIMMETT, M. R; IDDON, B.; SYNTHESIS AND REACTIONS OF LITHIATED MONOCYCLIC AZOLES CONTAINING TWO OR MORE HETERO
  146583. ATOMS. PART 3: PYRAZOLES.  HETEROCYCLES 1994, 37(3), 2087
  146584. 147. A REVIEWa
  146585. GABRIEL WEATHERHEAD
  146586. 6166N
  146587. 2/28/96VzKORBONITS, D.; HORV
  146588. TH, K.; SYNTHESIS OF HETEROCYCLES FROM AMINOAMIDE OXIMES.  HETEROCYCLES 1994, 37(3), 2051
  146589. 68. A REVIEWa
  146590. GABRIEL WEATHERHEAD
  146591. 6167N
  146592. 2/28/96
  146593. BELEN'KII, L. I.; RELATIVE STABILITIES OF HETARENIUM IONS 
  146594.  FACTORS CONTROLLING POSITIONAL SELECTIVITIES OF ELECTROPHILIC SUBSTITUTION AND ACID
  146595. INDUCED TRANSFORMATIONS OF PYRROLE, FURAN AND THIO PHENE DERIVATIVES.  HETEROCYCLES 1994, 37(3), 2029
  146596. 49. A REVIEW
  146597. GABRIEL WEATHERHEAD
  146598. 6168N
  146599. 2/28/96VZMCNAB, H.; THORNLEY, C.; PYRROLIZIN
  146600. ONES.  HETEROCYCLES 1994, 37(3), 1977
  146601. 2008. A REVIEWa
  146602. GABRIEL WEATHERHEAD
  146603. 6169N
  146604. 2/28/96
  146605. BALASUBRAMANIAN, M.; KEAY, J. G.; SCRIVEN, E. F. V.; SHOBANA, N. APPROACHES TO THE SYNTHESIS OF 1
  146606. SUBSTITUTED 1,2,4
  146607. TRIAZOLES.  HETEROCYCLES 1994, 37(3), 1951
  146608. 75. A REVIEWa
  146609. GABRIEL WEATHERHEAD
  146610. 6170N
  146611. 2/28/96V
  146612. ROBOZ, J.; DIAGNOSIS AND MONITORING OF DISSEMINATED CANDIDIASIS BASED ON SERUM/URINE D/L ARABINITOL RATIOS.  CHIRALITY 1994, 6(2),51
  146613. 57. A REVIEWa
  146614. GABRIEL WEATHERHEAD
  146615. 6171N
  146616. 2/28/96V
  146617. ROGAN, M. M.; ALTRIA, K. D.; GOODALL, D. M.; ENANTIOSELECTIVE SEPARATIONS USING CAPILLARY ELECTROPHORESIS.  CHIRALITY 1994, 6(1), 25
  146618. 40. A REVIEWa
  146619. GABRIEL WEATHERHEAD
  146620. 6172N
  146621. 2/28/96VjIZUMI, Y.; IWASAWA, Y.; CO
  146622. BREATHING RUTHENIUM AND RHODIUM CLUSTERS.  CHEMTECH 1994, 24(7), 20
  146623. 7. A REVIEWa
  146624. GABRIEL WEATHERHEAD
  146625. 6173N
  146626. 2/28/96
  146627. MURUGAN, R.; GRENDZE, M. P.; TOOMEY, J. E., JR.; KATRITZKY, A. R.; KARELSON, M.; LOBANOV, V.; RACHWAL, P.; PREDICTING PHYSICAL PROPERTIES FROM MOLECULAR STRUCTURE.  CHEMTECH 1994, 24(6), 17
  146628. 23. A REVIEWa
  146629. GABRIEL WEATHERHEAD
  146630. 6174N
  146631. 2/28/96VeMILGROM, L. R.; VITAMIN B12 : THE VIEW FROM THE SUMMIT.  CHEM. IN BRIT. 1994, 31(11), 923
  146632. 7. A REVIEWa
  146633. GABRIEL WEATHERHEAD
  146634. 6175N
  146635. 2/28/96VSTURNER, N. J.; BIOCATALYTIC REDUCTIONS.  CHEM. AND IND. 1994. (15), 592
  146636. 5. A REVIEWa
  146637. GABRIEL WEATHERHEAD
  146638. 6176N
  146639. 2/28/96VdMOORE, J. S.; LEE, S.; CRAFTING MOLECULAR BASED SOLIDS.  CHEM. AND IND. 1994. (14), 556
  146640. 60. A REVIEWa
  146641. GABRIEL WEATHERHEAD
  146642. 6177N
  146643. 2/28/96VkWILLS, M.; STUDLEY, J. R.; THE ASYMMETRIC REDUCTION OF KETONES.  CHEM. AND IND. 1994. (14), 552
  146644. 5. A REVIEWa
  146645. GABRIEL WEATHERHEAD
  146646. 6178N
  146647. 2/28/96
  146648. BLACKBURN, G. M.; WENTWORTH, P.; CATALYTIC ANTIBODIES : THE GENERATION OF NOVEL BIOCATALYSTS.  CHEM. AND IND. 1994. (9), 338
  146649. 42. A REVIEWa
  146650. GABRIEL WEATHERHEAD
  146651. 6179N
  146652. 2/28/96ViJOEL, S. P.; TAXOL AND TAXOTERE : FROM YEW TREE TO TUMOUR CELL. CHEM. AND IND. 1994. (5), 172
  146653. 5. A REVIEWa
  146654. GABRIEL WEATHERHEAD
  146655. 6180N
  146656. 2/28/96V[CONSTABLE, E. C.; METALLOSUPRAMOLECULAR CHEMISTRY. CHEM. AND IND. 1994, (2), 56
  146657. 9. A REVIEWa
  146658. GABRIEL WEATHERHEAD
  146659. 6181N
  146660. 2/28/96V{PALOU, J.; OXIDATION OF SOME ORGANIC COMPOUNDS BY AQUEOUS BROMINE SOLUTIONS.  CHEM. SOC. REV. 1994, 23(5), 357
  146661. 62. A REVIEWa
  146662. GABRIEL WEATHERHEAD
  146663. 6182N
  146664. 2/28/96V
  146665. ADAMS, R. D.; THE INSERTION OF ALKYNES INTO METAL
  146666. METAL BONDS AND ORGANIC CHEMISTRY OF THE DIMETALLED OLEFIN COMPLEXES.  CHEM. SOC. REV. 1994, 23(5), 335
  146667. 9. A REVIEWa
  146668. GABRIEL WEATHERHEAD
  146669. 6183N
  146670. 2/28/96
  146671. VtSAMMES, P. G.; YAHIOGLU, G.; 1,10
  146672. PHENANTHROLINE: A VERSATILE LIGAND.  CHEM. SOC. REV. 1994, 23(5), 327
  146673. 34. A REVIEWa
  146674. GABRIEL WEATHERHEAD
  146675. 6184N
  146676. 2/28/96V
  146677. ALMOND, M. J.; PHOTOOXIDATION REACTIONS OF TRANSITION METAL CARBONYLS IN LOW
  146678. TEMPERATURE MATRICE;  CHEM. SOC. REV. 1994, 23(5), 309
  146679. 17. A REVIEWa
  146680. GABRIEL WEATHERHEAD
  146681. 6185N
  146682. 2/28/96V
  146683. DIEDERICH, F.; ISAACS, L.; PHILP, D.; SYNTHESIS, STRUCTURES, AND PROPERTIES OF METHANOFULLERENES,  CHEM. SOC. REV. 1994, 23(4), 243
  146684. 55. A REVIEWa
  146685. GABRIEL WEATHERHEAD
  146686. 6186N
  146687. 2/28/96V
  146688. SCHNEIDER, H.
  146689. J.; LINEAR FREE ENERGY RELATIONSHIPS AND PAIRWISE INTERACTIONS IN SUPRAMOLECULAR CHEMISTRY.  CHEM. SOC. REV. 1994, 23(4), 227
  146690. 34. A REVIEWa
  146691. GABRIEL WEATHERHEAD
  146692. 6187N
  146693. 2/28/96V
  146694. MEHROTRA, R. C.; SINGH, A.; SOGANI, S.; HOMO
  146695.  AND HETERO
  146696. METALLIC ALKALOIDS OF GROUP 1, 2 AND 12 METALS.  CHEM. SOC. REV. 1994, 23(3), 215
  146697. 25. A REVIEWa
  146698. GABRIEL WEATHERHEAD
  146699. 6188N
  146700. 2/28/96V
  146701. CRAYSTON, J. A.; IRAQI, A.; WALTON, J. C.; POLYRADICALS : SYNTHESIS, SPECTROSCOPY AND CATALYSIS.  CHEM. SOC. REV. 1994, 23(3), 147
  146702. 53. A REVIEWa
  146703. GABRIEL WEATHERHEAD
  146704. 6189N
  146705. 2/28/96V
  146706. MEHROTRA, R. C.; SINGH, A.; SOGANI, S.; RECENT ADVANCES IN THE CHEMISTRY OF HOMO
  146707.  AND HETEROMETALLIC ALKOXIDES OF P
  146708. BLOCK METAL(LOID)S,  CHEM. REV. 1994, 94(6), 1643
  146709. 60. A REVIEWa
  146710. GABRIEL WEATHERHEAD
  146711. 6190N
  146712. 2/28/96V~ZUMAN, P.; SHAH, B.; ADDITION, REDUCTION AND OXIDATION REACTIONS OF NITROSOBENZENE.  CHEM. REV. 1994, 94(6), 1621
  146713. 41. A REVIEWa
  146714. GABRIEL WEATHERHEAD
  146715. 6191N
  146716. 2/28/96V
  146717. JUNGHEIM, L. N.; SHEPHERD, T. A.; DESIGN OF ANTITUMOR PRODRUGS: SUBSTRATES FOR ANTIBODY TARGETED ENZYMES.  CHEM. REV. 1994, 94(6), 1553
  146718. 66. A REVIEWa
  146719. GABRIEL WEATHERHEAD
  146720. 6192N
  146721. 2/28/96V
  146722. GUPTA, S. P.; QUANTITATIVE STRUCTURE
  146723. ACTIVITY RELATIONSHIP STUDIES ON ANTICANCER DRUGS.  CHEM. REV. 1994, 94(6), 1507
  146724. 51. A REVIEW
  146725. GABRIEL WEATHERHEAD
  146726. 6193N
  146727. 2/28/96V
  146728. HADJIPAVLOU
  146729. LITINA, D.; HANSCH, C.; QUANTITATIVE STRUCTURE
  146730. ACTIVITY RELATIONSHIPS OF THE BENZODIAZEPINES. A REVIEW AND REEVALUATION.  CHEM. REV. 1994, 94(6), 1483
  146731. 505. A REVIEWa
  146732. GABRIEL WEATHERHEAD
  146733. 6194N
  146734. 2/28/96V
  146735. GAUMONT, A. C.; DENIS, J.
  146736. M.; PREPARATION, CHARACTERIZATION AND SYNTHETIC POTENTIAL OF UNSTABLE COMPOUNDS CONTAINING PHOSPHORUS
  146737. CARBON MULTIPLE BONDS.  CHEM. REV. 1994, 94(5), 1413
  146738. 39. A REVIEWa
  146739. GABRIEL WEATHERHEAD
  146740. 6195N
  146741. 2/28/96V
  146742. GORENSTEIN, D. G.; CONFORMATION AND DYNAMICS OF DNA AND PROTEIN
  146743.  DNA COMPLEXES BY 31P NMR.  CHEM. REV. 1994, 94(5), 1315
  146744. 38. A REVIEWa
  146745. GABRIEL WEATHERHEAD
  146746. 6196N
  146747. 2/28/96V
  146748. CAVELL K. J. METAL CHELATE SYSTEMS AS CATALYSTS FOR OLEFIN AND CARBON
  146749. MONOXIDE CONVERSION REACTIONS.  AUST. J. CHEM. 1994, 47(5), 769
  146750. 97. A REVIEWa
  146751. GABRIEL WEATHERHEAD
  146752. 6197N
  146753. 2/28/96
  146754. CORNILS, B.; HERRMANN, W. A.; RASCH, M.; OTTO, R., PIONEER IN INDUSTRIAL HOMOGENEOUS CATALYSIS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(21), 2144
  146755. 63. A REVIEWa
  146756. GABRIEL WEATHERHEAD
  146757. 6198N
  146758. 2/28/96V
  146759. FAWCETT, W. R.; OPALLO, M.; THE KINETICS OF HETEROGENEOUS ELECTRON TRANSFER REACTIONS IN POLAR SOLVENTS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(21), 2131
  146760. 43. A REVIEWa
  146761. GABRIEL WEATHERHEAD
  146762. 6199N
  146763. 2/28/96V
  146764. ESSER, P.; POHLMANN, B.; SCHARF, H.
  146765. D.; THE PHOTOCHEMICAL SYNTHESIS OF FINE CHEMICALS WITH SUNLIGHT.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(20), 2009
  146766. 23. A REVIEWa
  146767. GABRIEL WEATHERHEAD
  146768. 6200N
  146769. 2/28/96V
  146770. HENSCHLER, D.; TOXICITY OF CHLORINATED ORGANIC COMPOUNDS : EFFECTS OF THE INTRODUCTION OF CHLORINE IN ORGANIC MOLECULES.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(19), 1920
  146771. 35. A REVIEWa
  146772. GABRIEL WEATHERHEAD
  146773. 6201N
  146774. 2/28/96
  146775. ULLRICH, V.; BRUGGER, R.; PROSTACYCLIN AND THROMBOXANE SYNTHASE: NEW ASPECTS OF HEMETHIOLATE CATALYSIS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(19), 1911
  146776. 19. A REVIEWa
  146777. GABRIEL WEATHERHEAD
  146778. 6202N
  146779. 2/28/96V
  146780. PADWA, A.; AUSTIN, D. J.; LIGAND EFFECTS ON THE CHEMOSELECTIVITY OF TRANSITION METAL CATALYZED REACTIONS OF A
  146781. DIAZO CARBONYL COMPOUNDS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(18), 1797
  146782. 815. A REVIEWa
  146783. GABRIEL WEATHERHEAD
  146784. 6203N
  146785. 2/28/96VuGANTE, J.; PEPTIDOMIMETICS 
  146786.  TAILORED ENZYME INHIBITORS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(17), 1699
  146787. 720. A REVIEWa
  146788. GABRIEL WEATHERHEAD
  146789. 6204N
  146790. 2/28/96ViLASIC, D. D.; STERICALLY STABILIZED VESICLES.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(17), 1685
  146791. 98. A REVIEWa
  146792. GABRIEL WEATHERHEAD
  146793. 6205N
  146794. 2/28/96
  146795. GIBSON, V. C.; LIGANDS AS "COMPASS NEEDLES": HOW ORIENTATIONS OF ALKENE, ALKYNE AND ALKYLIDENE LIGANDS REVEAL P
  146796. BONDING FEATURES IN TETRAHEDRAL TRANSITION METAL COMPLEXES.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(15/16), 1565
  146797. 72. A REVIEWa
  146798. GABRIEL WEATHERHEAD
  146799. 6206N
  146800. 2/28/96V
  146801. EFFENBERGER, F.; SYNTHESIS AND REACTIONS OF OPTICALLY ACTIVE CYANOHYDRINS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(15/16), 1555
  146802. 64. A REVIEWa
  146803. GABRIEL WEATHERHEAD
  146804. 6207N
  146805. 2/28/96V
  146806. COLLMAN, J. P.; WAGENKNECHT, P. S.; HUTCHINSON, J. E.; MOLECULAR CATALYSTS FOR MULTIELECTRON REDOX REACTIONS OF SMALL MOLECULES: THE "COFACIAL METALLODIPORPHYRIN" APPROACH.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(15/16), 1537
  146807. 54. A REVIEWa
  146808. GABRIEL WEATHERHEAD
  146809. 6208N
  146810. 2/28/96V
  146811. YAMAZAKI, T.; BENEDETTI, E.; KENT, D.; GOODMAN, M.; CONFORMATIONAL REQUIREMENTS FOR SWEET
  146812. TASTING PEPTIDES AND PEPTIDOMIMETICS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(14), 1437
  146813. 52. A REVIEW
  146814. GABRIEL WEATHERHEAD
  146815. 6209N
  146816. 2/28/96VhFISCHER, G.; ISOMERASES AND THEIR EFFECTORS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(14), 1415
  146817. 36. A REVIEWa
  146818. GABRIEL WEATHERHEAD
  146819. 6210N
  146820. 2/28/96V
  146821. BILLUPS, W. E.; MCCORD, D. J.; GAS
  146822. PHASE SYNTHESIS OF REACTIVE MOLECULES USING ADSORBED REAGENTS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(13), 1332
  146823. 43. A REVIEWa
  146824. GABRIEL WEATHERHEAD
  146825. 6211N
  146826. 2/28/96V
  146827. LENTZ, D.; FLUORINATED ISOCYANIDES 
  146828.  MORE THAN LIGANDS WITH UNUSUAL PROPERTIES.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(13), 1315
  146829. 31. A REVIEWa
  146830. GABRIEL WEATHERHEAD
  146831. 6212N
  146832. 2/28/96V
  146833. LAMBERT, C.; SCHLEYER, P. VON R.; ARE POLAR ORGANOMETALLIC COMPOUNDS "CARBANIONS"? THE GEGENION EFFECT ON STRUCTURE AND ENERGIES OF ALKALI
  146834. METAL COMPOUNDS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(11), 1129
  146835. 40. A REVIEWa
  146836. GABRIEL WEATHERHEAD
  146837. 6213N
  146838. 2/28/96
  146839. VnWEBER, L.; HOMOLEPTIC NOBLE METAL CARBONYL CATIONS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(10), 1077
  146840. 8. A REVIEWa
  146841. GABRIEL WEATHERHEAD
  146842. 6214N
  146843. 2/28/96V
  146844. BUNZ, U. H. F.; POLYYNES 
  146845.  FASCINATING MONOMERS FOR THE CONSTRUCTION OF CARBON NETWORKS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(10), 1073
  146846. 6. A REVIEWa
  146847. GABRIEL WEATHERHEAD
  146848. 6215N
  146849. 2/28/96V
  146850. MAYR, H.; PATZ, M.; SCALES OF NUCLEOPHILICITY AND ELECTROPHILICITY: A SYSTEM FOR ORDERING POLAR ORGANIC AND ORGANOMETALLIC REACTIONS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(9), 938
  146851. 58. A REVIEWa
  146852. GABRIEL WEATHERHEAD
  146853. 6216N
  146854. 2/28/96VeTHOMAS, M. J.; TURNING POINTS IN CATALYSIS.  ANGEW. CHEM. INT. ED. ENG. 1994, 33(9), 913
  146855. 37. A REVIEWa
  146856. GABRIEL WEATHERHEAD
  146857. 6217N
  146858. 2/28/96V
  146859. DAHL, T.; THE NATURE OF STACKING INTERACTIONS BETWEEN ORGANIC MOLECULES ELUCIDATED BY ANALYSIS OF CRYSTAL STRUCTURES. ACTA CHEM SCAND 1994, 48, 95
  146860. 106. A REVIEWa
  146861. GABRIEL WEATHERHEAD
  146862. 6218N
  146863. 2/28/96V
  146864. COOKS, R. G.; AST, T.; PRADEEP, T.; WYSOCKI, V.; REACTIONS OF IONS WITH ORGANIC
  146865. SURFACES. ACCT CHEM. RES. 1994, 27(11), 316
  146866. 23. A REVIEWa
  146867. GABRIEL WEATHERHEAD
  146868. 6219N
  146869. 2/28/96V
  146870. BURROWS, C. J.; ROKITA, S. E.; RECOGNITION OF GUANINE STRUCTURE IN NUCLEIC ACIDS BY NICKEL
  146871. COMPLEXES. ACCT CHEM. RES. 1994, 27(10), 295
  146872. 301. A REVIEWa
  146873. GABRIEL WEATHERHEAD
  146874. 6220N
  146875. 2/28/96V
  146876. LIU, M. T. H.; LASER FLASH PHOTOLYSIS STUDIES: 1,2
  146877. HYDROGEN MIGRATION TO A CARBENE. ACCT CHEM. RES. 1994, 27(10), 287
  146878. 94. A REVIEWa
  146879. GABRIEL WEATHERHEAD
  146880. 6221N
  146881. 2/28/96VhCOLLINS, T. J.; DESIGNING LIGANDS FOR OXIDIZING COMPLEXES. ACCT CHEM. RES. 1994, 27(9), 279
  146882. 85. A REVIEWa
  146883. GABRIEL WEATHERHEAD
  146884. ORG PREP PROCEDURE INTC    ELGUERO JM
  146885. 6222N
  146886. 2/28/96VATRIFLUOROMETHYL AND PERFLUOROALKYL DERIVATIVES OF AZOLES.A REVIEWW
  146887. 1995 FEBX
  146888.  27(1)a
  146889. GABRIEL WEATHERHEAD
  146890. CHEM COMMUN
  146891. CUMESSEGUER CHEMOSELECTIVE EPOXIDATION EPOXIDE OXIDATION DIOXIRANE AMINE N
  146892. OXIDE REVIEWM
  146893. 6223N
  146894. 2/28/96V]USE OF DIOXIRANES FOR THE CHEMOSELECTIVE OXIDATION OF TERTIARY AMINES BEARING ALKENE MOIETIESW
  146895. 1995 P 293a
  146896. GABRIEL WEATHERHEAD
  146897. ACCTS CHEM RESC`HOUK PERICYCLIC CONCERTED REVIEW CYCLOADDITION DIPOLAR COPE DIRADICAL CALCULATION WRITING THEORYM
  146898. 6224N
  146899. 2/28/96V%PERICYCLIC REACTION TRANSITION STATESW    1995 P 81a
  146900. GABRIEL WEATHERHEAD
  146901. J ORG CHEMCrCOXON HOUK CRAM FELKIN
  146902. ANH KARABATSOS REVIEW MODEL CARBONYL STEREOCHEM CIEPLAK FMO CALCULATIONS FACIAL SELECTIVITYM
  146903. 6225N
  146904. 2/28/96VYFACTORS WHICH CONTROL PI FACIAL SELECTION IN THE REDUCTION OF 5
  146905. SUBSTITUTED ADAMANTANONESW
  146906. VOL 60 1995 P 418a
  146907. GABRIEL WEATHERHEAD
  146908. SYNLETTC;MAIER REVIEW ENEYNE DRUG BERGMAN DIRADICAL TRIGGER AROMATICM
  146909. 6226N
  146910. 2/28/96V
  146911. DESIGN OF ENEDIYNE PRODRUGSW    1995 P 13a
  146912. GABRIEL WEATHERHEAD
  146913. SYNLETT
  146914. C]KLUMP REVIEW HETEROCYCLIC PALLADIUM ALLYL ZINC CYCLIZATION TRIMETHYLENE METHANE REAGENT TROSTM
  146915. 6227N
  146916. 2/28/96VrPREPARATION OF CARBOCYCLIC AND HETEROCYCLIC COMPOUNDS BY THE USE OF AN ALLYL ZINC AND AN ALLYL PALLADIUM IN TANDEMW
  146917. 1995 P 1a
  146918. GABRIEL WEATHERHEAD
  146919. SYNLETTClMORI ENE YNE METAL METATHESIS REVIEW CYCLIZATION INTRAMOLECULAR AMINE GRUBBS WRITING ENYNE RUTHENIUM RHODIUMM
  146920. 6228N
  146921. 2/28/96V$RUTHENIUM CATALYZED ENYNE METATHESISW
  146922. 1994 P 1020a
  146923. GABRIEL WEATHERHEAD
  146924. SYNLETTCGKATAOKA KETO SULFONE REVIEW PREPARATION IMINE SULFENE ENAMINE SYNTHESISM
  146925. 6229N
  146926. 2/28/96VfA NEW SYNTHESIS OF BETA KETO AND BETA FORMYL SULFONES BY THE REACTION OF IMINES AND SULFONYL CHLORIDESW
  146927. 1994 P 1017a
  146928. GABRIEL WEATHERHEAD
  146929. SYNLETTC{WICHA SILICON SILYL EPOXIDE ANION GROUP TRANSFER REARRANGEMENT DISPLACEMENT CYCLOPROPENE REVIEW ALKOXIDE ELIMINATION ALKENEM
  146930. 6230N
  146931. 2/28/96
  146932. VvTANDEM TRANSFORMATIONS INITIATED BY THE MIGRATION OF A SILYL GROUP.  SOME NEW SYNTHETIC APPLICATIONS OF SILYL OXIRANESW
  146933. 1994 P 985a
  146934. GABRIEL WEATHERHEAD
  146935. ACC CHEM RESC`CABRI HECK PALLADIUM REVIEWS LIGAND CATALYST CATALYSED MECHANISM OXIDATIVE ADDITION VINYL ALKENEM
  146936. 6231N
  146937. 2/28/96V=RECENT DEVELOPMENTS AND NEW PERSPECTIVES IN THE HECK REACTIONW
  146938. VOL 28 1995 P 2a
  146939. GABRIEL WEATHERHEAD
  146940. J ORG CHEMCqTAKEUCHI WITTIG REACTION STEREOSELECTIVITY PHOSPHOROUS YLIDE STEREOCHEM CIS TRANS STABILIZED REVIEW NONSTABILIZEDM
  146941. 6232N
  146942. 2/28/96ViSTEREOSELECTIVITY IN THE WITTIG REACTION OF AROMATIC KETONES ORIGIN OF PREFERENCE FOR THE OLEFIN GEOMETRYW
  146943. VOL 60 1995 P 156a
  146944. GABRIEL WEATHERHEAD
  146945. JACSCIRADOM DIAZO KETONE WOLFF REARRANGEMENT OXIRENE KETO CARBENE REVIEW THEORYM
  146946. 6233N
  146947. 2/28/96V8THE WOLFF REARRANGEMENT.  OXIRENE
  146948. KETENE INTERCONVERSIONW
  146949. VOL 116 1994 P 10159a
  146950. GABRIEL WEATHERHEAD
  146951. ORG PREP PROCEDURE INT
  146952. PATWARDHAN SAM
  146953. 6234N
  146954. 2/28/96V.SYNTHESIS OF ALPHA,OMEGA
  146955. ALKANEDIOLS. A REVIEWW
  146956. 1994 DECX
  146957.  26(6)a
  146958. GABRIEL WEATHERHEAD
  146959. TETRAHEDRONCUA REVIEW ON ALL RECENT ROUTES TO BETA AMINO ACIDS ENANTIOSELECTIVE AND OTHERS  COLE DM
  146960. 6235N
  146961. 2/28/96V$ASYMMETRIC SYNTHESIS OF B
  146962. AMINOACIDSW
  146963. 1994  50  9517a
  146964. GABRIEL WEATHERHEAD
  146965. CHEM REVIEWSC
  146966. REVIEW WITH EXTENSIVE REFERENCES OF ALL  TYPES OF DIAZO CARBONYLS WOLFF REARRANGEMENT TRANSITION METAL CATALYZED REACTIONS  M.A. MCKERVEYM
  146967. 6236N
  146968. 2/28/96V
  146969. CYCLIZATIONS WITH DIAZOKETONESW
  146970. 1994  94   1091a
  146971. GABRIEL WEATHERHEAD
  146972. ANGEW CHEM INT EDCbA REVIEW ON TRHE SYNTHETIC USES OF CHIRAL AZITRIDINES AS PRECURSORS FOR CHIRAL MOLECULES  TANNER DM
  146973. 6237N
  146974. 2/28/96V
  146975. CHIRAL AZIRIDINES
  146976. A REVIEWW
  146977. 1994 33  599a
  146978. GABRIEL WEATHERHEAD
  146979. TETRAHEDRONCoA SURVEY OF VARIOUS STOICHIOMETRIC AND CATALYTIC ASYMMETRIC SYNTHESES AND THEIR INDUSTRIAL POSSIBILITIES  KOTHAM
  146980. 6238N
  146981. 2/28/96
  146982. V4REVIEW   ASYMMETRIC SYNTHESIS AN INDUSTRIAL PROSPECTW
  146983. 1994  3639a
  146984. GABRIEL WEATHERHEAD
  146985. TETRAHEDRONC
  146986. A REVIEW RING EXPANSION METHODS USING YLIDES ARENE
  146987. ALKYNE  2+2 PRODUCTS PHOTOADDITION AMINO LACTAMS OPTICALLY ACTIVE ETHER LACTAMS PATERNO
  146988. BUCHI SPIRO QUATERNARY AMMONIUM SALTS ROXBURGH C.JM
  146989. 6239N
  146990. 2/28/96V$MEDIUM SIZED RINGS BY RING EXPANSIONW
  146991. 1993  49  10749a
  146992. GABRIEL WEATHERHEAD
  146993. ANGEW CHEMC
  146994. SEQUENTIAL MICHAEL ADDITIONS POLYCYCLIC COMPOUNDS MICHAEL
  146995. ALDOL MICHAEL
  146996. MICHAEL
  146997. MICHAEL POLYCYCLIC NATURAL PRODUCTS REVIEW FUKUMOTOM
  146998. 6240N
  146999. 2/28/96V'INTRAMOLECULAR MICHAEL ADDITIONS REVIEWW
  147000. 1993 32 1010a
  147001. GABRIEL WEATHERHEAD
  147002. HETEROCYCLESC!REVIEW ON OXAZOLES ALFRED HASSNERM
  147003. 6241N
  147004. 2/28/96V#NEW CHEMISTRY OF OXAZOLES
  147005.  A REVIEWW
  147006. 1993 35 1441a
  147007. GABRIEL WEATHERHEAD
  147008. B    SYNTHESISCqSILYL DIENES WITTIG REACTIONS PETERSON REACTIONE VINYL HALIDES DIENES  ENEYNES DIELS
  147009. ALDER DITHIOACETALS  LUH T
  147010. 6242N
  147011. 2/28/96
  147012. V.SILYL  SUBSTITUTED CONJUGATED DIENES
  147013.  A REVIEWW
  147014. 1993   349a
  147015. GABRIEL WEATHERHEAD
  147016. ORG PREP PROCEDURE INTC
  147017. WITTENBERGER SJM
  147018. 6243N
  147019. 2/28/96V5RECENT DEVELOPMENTS IN TETRAZOLE CHEMISTRY 
  147020.  A REVIEWW
  147021. 1994 OCTX
  147022.  26(5)a
  147023. GABRIEL WEATHERHEAD
  147024. CHEM REVC
  147025. HADJIPAVLOULITINA DM
  147026. 6244N
  147027. 2/28/96V`QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIPS OF THE BENZODIAZEPINES 
  147028.  A REVIEW AND REEVALUATIONW
  147029. 1994 SEP
  147030.  1483
  147031. 1505Y
  147032.  94(6)a
  147033. GABRIEL WEATHERHEAD
  147034. 6245N
  147035. 2/28/96V
  147036. ZANELLO, PIERO, ED. CHAINS, CLUSTERS, INCLUSION COMPOUNDS, PARAMAGNETIC LABELS, AND ORGANIC RINGS. (STEREOCHEMISTRY OF ORGANOMETALLIC AND INORGANIC COMPOUNDS, VOL. 5). ELSEVIER: AMSTERDAM, 1994. A REVIEWa
  147037. GABRIEL WEATHERHEAD
  147038. 6246N
  147039. 2/28/96VtWONG, CHI
  147040. HUEY; WHITESIDES, GEORGE M. ENZYMES IN SYNTHETIC ORGANIC CHEMISTRY. PERGAMON: OXFORD, U.K., 1994. A REVIEWa
  147041. GABRIEL WEATHERHEAD
  147042. 6247N
  147043. 2/28/96
  147044. V|WARD, ROBERT S. BIFUNCTIONAL COMPOUNDS (OXFORD CHEMISTRY PRIMERS 17). OXFORD UNIVERSITY PRESS: OXFORD, U. K., 1994. A REVIEWa
  147045. GABRIEL WEATHERHEAD
  147046. 6248N
  147047. 2/28/96V[VOLKE, J; LISKA, F. ELECTROCHEMISTRY IN ORGANIC SYNTHESIS. SPRINGER: BERLIN, 1994. A REVIEWa
  147048. GABRIEL WEATHERHEAD
  147049. 6249N
  147050. 2/28/96VUTEISSEIRE, PAUL JOSE. CHEMISTRY OF FRAGRANT SUBSTANCES. VCH: NEW YORK, 1994. A REVIEWa
  147051. GABRIEL WEATHERHEAD
  147052. 6250N
  147053. 2/28/96V
  147054. STARKS, CHARLES M.; LIOTTA, CHARLES L.; HALPERN, MARC. PHASE
  147055. TRANSFER CATALYSIS. FUNDAMENTALS, APPLICATIONS, AND INDUSTRIAL PERSPECTIVES. CHAPMAN & HALL: NEW YORK, 1994. A REVIEWa
  147056. GABRIEL WEATHERHEAD
  147057. 6251N
  147058. 2/28/96V~SHELDON, ROGER A. CHIROTECHNOLOGY: INDUSTRIAL SYNTHESIS OF OPTICALLY ACTIVE COMPOUNDS. MARCEL DEKKER: NEW YORK, 1993. A REVIEWa
  147059. GABRIEL WEATHERHEAD
  147060. 6252N
  147061. 2/28/96
  147062. VXSCHLOSSER, M., ED. ORGANOMETALLICS IN SYNTHESIS. WILEY: CHICHESTER, U.K., 1994. A REVIEWa
  147063. GABRIEL WEATHERHEAD
  147064. 6253N
  147065. 2/28/96V
  147066. RUFF, F. ORGANIC REACTIONS: EQUILIBRIA, KINETICS AND MECHANISM. (STUDIES IN ORGANIC CHEMISTRY, VOL. 50). ELSEVIER: AMSTERDAM, 1994. A REVIEWa
  147067. GABRIEL WEATHERHEAD
  147068. 6254N
  147069. 2/28/96V\RAUK, ARVI. ORBITAL INTERACTION THEORY OF ORGANIC CHEMISTRY. WILEY: NEW YORK, 1994. A REVIEWa
  147070. GABRIEL WEATHERHEAD
  147071. 6255N
  147072. 2/28/96V
  147073. RAHMAN, ATTA
  147074. UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 14: STEREOSELECTIVE SYNTHESIS, PART I. ELSEVIER: AMSTERDAM, 1994. A REVIEWa
  147075. GABRIEL WEATHERHEAD
  147076. 6256N
  147077. 2/28/96VZPETRAGNANI, NICOLA. TELLURIUM IN ORGANIC SYNTHESIS. ACADEMIC PRESS: LONDON, 1994. A REVIEWa
  147078. GABRIEL WEATHERHEAD
  147079. 6257N
  147080. 2/28/96VZPEARSON, A. J. IRON COMPOUNDS IN ORGANIC SYNTHESIS. ACADEMIC PRESS: LONDON, 1994. A REVIEWa
  147081. GABRIEL WEATHERHEAD
  147082. 6258N
  147083. 2/28/96
  147084. ;PANICO, ROBERT; POWELL, WARREN H., RICHER, JEAN CLAUDE, EDS. A GUIDE TO IUPAC NOMENCLATURE OF ORGANIC COMPOUNDS: RECOMMENDATIONS 1993. INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY (IUPAC) ORGANIC CHEMISTRY DIVISION, COMMISION ON NOMENCLATURE OF ORGANIC CHEMISTRY (III.1). BLACKWELL: OXFORD, U.K.,1993. A REVIEW
  147085. GABRIEL WEATHERHEAD
  147086. 6259N
  147087. 2/28/96V
  147088. OHLOFF, GUTHER. SCENT AND FRAGRANCES (TRANSLATION OF "RIECHSTOFFE UND GERUCHSINN" BY WILHELM PICKENHAGEN. AND BRIAN M. LAWRENCE). SPRINGER
  147089. VERLAG: BERLIN, 1994. A REVIEWa
  147090. GABRIEL WEATHERHEAD
  147091. 6260N
  147092. 2/28/96VlOHASHI, Y., ED. REACTIVITY IN MOLECULAR CRYSTALS. KODANSHA: TOKYO AND VCH: WEINHEIM, GERMANY, 1993. A REVIEWa
  147093. GABRIEL WEATHERHEAD
  147094. 6261N
  147095. 2/28/96V
  147096. OGURA, HARUO; HASEGAWA, AKIRA, SUAMI, TETSUO EDS. CARBOHYDRATES. SYNTHETIC METHODS AND APPLICATIONS IN MEDICINAL CHEMISTRY. KODANSHA: TOKYO AND VCH: WEINHEIM, GERMANY, 1992. A REVIEW
  147097. GABRIEL WEATHERHEAD
  147098. 6262N
  147099. 2/28/96V}NYE, MARY JO. FROM CHEMICAL PHILOSOPHY TO THEORETICAL CHEMISTRY. UNIVERSITY OF CALIFORNIA PRESS: BERKELEY, CA, 1993. A REVIEWa
  147100. GABRIEL WEATHERHEAD
  147101. 6263N
  147102. 2/28/96VYNOYORI, RYOJI. ASYMMETRIC CATALYSIS IN ORGANIC SYNTHESIS. WILEY: NEW YORK, 1994. A REVIEWa
  147103. GABRIEL WEATHERHEAD
  147104. 6264N
  147105. 2/28/96VpNOYORI, R. ORGANIC SYNTHESIS IN JAPAN: PAST PRESENT AND FUTURE. TOKYO KAGAKU DOZIN: TOKYO, JAPAN, 1992. A REVIEWa
  147106. GABRIEL WEATHERHEAD
  147107. 6265N
  147108. 2/28/96V
  147109. LUKACS, GABOR, ED. RECENT PROGRESS IN THE CHEMICAL SYNTHESIS OF ANTIBIOTICS AND RELATED MICROBIAL PRODUCTS, VOL. 2. SPRINGER
  147110. VERLAG: BERLIN, GERMANY, A REVIEWa
  147111. GABRIEL WEATHERHEAD
  147112. 6266N
  147113. 2/28/96V
  147114. KROTO, H. W.; WALTON, D, R. M., EDS. THE FULLERENES: NEW HORIZONS FOR THE CHEMISTRY, PHYSICS AND ASTROPHYSICS OF CARBON. CAMBRIDGE UNIVERSITY PRESS: NEW YORK, 1993. A REVIEWa
  147115. GABRIEL WEATHERHEAD
  147116. 6267N
  147117. 2/28/96V
  147118. IZQUIERDO, IVAN; MEDINA, JORGE, EDS. NATURALLY OCCURRING BENZODIAZEPINES. STRUCTURE, DISTRIBUTION AND FUNCTION. ELLIS HORWOOD: NEW YORK, 1993. A REVIEWa
  147119. GABRIEL WEATHERHEAD
  147120. 6268N
  147121. 2/28/96V
  147122. HORNBY, MICHAEL; PEACH, JOSEPHINE. FOUNDATIONS OF ORGANIC CHEMISTRY. (OXFORD UNIVERSITY PRIMERS 9). OXFORD UNIVERSITY PRESS: NEW YORK, 1993. A REVIEWa
  147123. GABRIEL WEATHERHEAD
  147124. 6269N
  147125. 2/28/96VJHO, TSE
  147126. LOK. TACTICS OF ORGANIC SYNTHESIS. WILEY: NEW YORK, 1994. A REVIEWa
  147127. GABRIEL WEATHERHEAD
  147128. 6270N
  147129. 2/28/96V
  147130. HASSNER, A.; STUMER, C. ORGANIC SYNTHESES BASED ON NAME REACTIONS AND UNNAMED REACTIONS. PERGAMON: OXFORD, U.K., 1994. A REVIEWa
  147131. GABRIEL WEATHERHEAD
  147132. 6271N
  147133. 2/28/96VtHARBORNE, JEFFREY BARRY, ED. THE FLAVONOIDS: ADVANCES IN RESEARCH SINCE 1986. CHAPMAN & HALL: LONDON, 1994. A REVIEWa
  147134. GABRIEL WEATHERHEAD
  147135. 6272N
  147136. 2/28/96
  147137. FUHRHOP, JURGEN; PENZLIN, GUSTAV. ORGANIC SYNTHESIS: CONCEPTS, METHODS, STARTING MATERIALS, 2ND ED. VCH: NEW YORK, 1994. A REVIEWa
  147138. GABRIEL WEATHERHEAD
  147139. 6273N
  147140. 2/28/96VcFABER, K. BIOTRANSFORMATIONS IN ORGANIC CHEMISTRY. SPRINGER
  147141. VERLAG: BERLIN, GERMANY, 1992. A REVIEWa
  147142. GABRIEL WEATHERHEAD
  147143. 6274N
  147144. 2/28/96VyELIEL, ERNEST L.; WILEN, SAMUEL H., MANDER LEWIS N. STEREOCHEMISTRY OF ORGANIC COMPOUNDS. WILEY: NEW YORK, 1994. A REVIEWa
  147145. GABRIEL WEATHERHEAD
  147146. 6275N
  147147. 2/28/96V|DIAS, JERRY RAY. MOLECULAR ORBITAL CALCULATIONS USING CHEMICAL GRAPH THEORY. SPRINGER
  147148. VERLAG: BERLIN GERMANY, 1993. A REVIEWa
  147149. GABRIEL WEATHERHEAD
  147150. 6276N
  147151. 2/28/96V
  147152. CLARK, JAMES H.; KYBETT, ADRIAN P.; MACQUARRIE DUNCAN J. SUPPORTED REAGENTS: PREPARATION, ANALYSIS AND APPLICATIONS. VCH: NEW YORK, 1992. A REVIEWa
  147153. GABRIEL WEATHERHEAD
  147154. 6277N
  147155. 2/28/96
  147156. CHALONER, PENNY A. HOMOGENEOUS HYDROGENATION. (CATALYSIS BY METAL COMPLEXES, VOL. 15). KLUWER: DORDRECHT, THE NETHERLANDS, 1994. A REVIEWa
  147157. GABRIEL WEATHERHEAD
  147158. 6278N
  147159. 2/28/96V
  147160. BUCKINGHAM, A. D.; LEGON, A. C.; ROBERTS, S. M. EDS. PRINCIPLES OF MOLECULAR RECOGNITION. BLACKIE ACADEMIC AND PROFESSIONAL: LONDON, 1993. A REVIEWa
  147161. GABRIEL WEATHERHEAD
  147162. 6279N
  147163. 2/28/96V
  147164. BRUNNER, HENRI; ZETTLMEIER, WOLFGANG. HANDBOOK OF ENANTIOSELECTIVE CATALYSIS. VOL. I: PRODUCTS AND CATALYSTS; VOL. II: LIGANDS. REFERENCES. VCH: WEINHEIM, GERMANY, 1993. A REVIEWa
  147165. GABRIEL WEATHERHEAD
  147166. 6280N
  147167. 2/28/96VmBLAU, KARL; HALKET, JOHN. HANDBOOK OF DERIVATIVES FOR CHROMATOGRAPHY, 2ND ED. WILEY: NEW YORK, 1993. A REVIEWa
  147168. GABRIEL WEATHERHEAD
  147169. 6281N
  147170. 2/28/96V
  147171. BILLINGTON, D. C. THE INOSITOL PHOSPHATES: CHEMICAL SYNTHESIS AND BIOLOGICAL SIGNIFICANCE. VCH: WEINHEIM, GERMANY, 1993. A REVIEWa
  147172. GABRIEL WEATHERHEAD
  147173. 6282N
  147174. 2/28/96V
  147175. AYER, WILLIMA A.; TRIFONOV, LATCHEZAR, S. LICOPODIUM ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 45. GOEFFREY A. CORDELL AND A. BROSSI, EDS. ACADEMIC PRESS: NEW YORK, 1994. A REVIEWa
  147176. GABRIEL WEATHERHEAD
  147177. 6283N
  147178. 2/28/96V
  147179. SZANTAY, CSABA; DORNYEI, GABOR; BLASKO, GABOR. THE MORPHINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 45. GOEFFREY A. CORDELL AND A. BROSSI, EDS. ACADEMIC PRESS: NEW YORK, 1994. A REVIEWa
  147180. GABRIEL WEATHERHEAD
  147181. 6284N
  147182. 2/28/96
  147183. SCHAFER, ANDREA; BENZ, HERBERT; FIEDLER, WOLFGANG; GUGGISBERG, ARMIN; BIENZ, STEFAN; HESSE, MANFRED. POLYAMINE TOXINS FROM SPIDERS AND WASPS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 45. GOEFFREY A. CORDELL AND A. BROSSI, EDS. ACADEMIC PRESS: NEW YORK, 1994. A REVIEW
  147184. GABRIEL WEATHERHEAD
  147185. 6285N
  147186. 2/28/96
  147187. BAKER, GREGORY R.; YOUNG, JAMES K. A SYSTEMATIC NOMENCLATURE FOR CASCADE (DENDRITIC) POLYMERS. ADVANCES IN DENDRITIC MACROMOLECULES. VOLUME 1. GEORGE R. NEWKOME, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  147188. GABRIEL WEATHERHEAD
  147189. 6286N
  147190. 2/28/96V
  147191. RAJCA, ANDRZEJ. HIGH
  147192. SPIN POLYARYLMETHYL POLYRADICALS. ADVANCES IN DENDRITIC MACROMOLECULES. VOLUME 1. GEORGE R. NEWKOME, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  147193. GABRIEL WEATHERHEAD
  147194. 6287N
  147195. 2/28/96
  147196. NEENAN, THOMAS X.; MILLER, TIMOTHY M., KWOCK, ELIZABETH W.; BAIR, HARVEY E. PREPARATION AND PROPERTIES OF MONODISPERSE AROMATIC DENDRITIC MACROMOLECULES. ADVANCES IN DENDRITIC MACROMOLECULES. VOLUME 1. GEORGE R. NEWKOME, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEW
  147197. GABRIEL WEATHERHEAD
  147198. 6288N
  147199. 2/28/96
  147200. XU, ZHIFU; KYAN, BENJAMIN; MOORE, JEFFREY S. STIFF DENDRITIC MACROMOLECULES BASED ON POLYACETYLENES. ADVANCES IN DENDRITIC MACROMOLECULES. VOLUME 1. GEORGE R. NEWKOME, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  147201. GABRIEL WEATHERHEAD
  147202. 6289N
  147203. 2/28/96V
  147204. MOOREFIELD, CHARLES N.; NEWKOME, GEORGE R. A REVIEW OF DENDRITIC MACROMOLECULES. ADVANCES IN DENDRITIC MACROMOLECULES. VOLUME 1. GEORGE R. NEWKOME, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  147205. GABRIEL WEATHERHEAD
  147206. 6290N
  147207. 2/28/96V
  147208. SINGH, NAKSHATRA B.; SINGH, RAM J.; SINGH, NARENDRA P. ORGANIC SOLID STATE REACTIVITY. TETRAHEDRON, 1994, 50(22), 6441
  147209. 93. A REVIEWa
  147210. GABRIEL WEATHERHEAD
  147211. 6291N
  147212. 2/28/96V
  147213. KANE, VINAYAK V.; DE WOLF, WILLEM H.; BICKELHAUPT, FRIEDRICH. SYNTHESIS OF SMALL CYCLOPHANES. TETRAHEDRON, 1994,50(16),4575
  147214. 622. A REVIEWa
  147215. GABRIEL WEATHERHEAD
  147216. 6292N
  147217. 2/28/96
  147218. VtNOYORI, RYOJI. ORGANOMETALLIC WAYS FOR THE MULTIPLICATION OF CHIRALITY. TETRAHEDRON, 1994, 50(15), 4259
  147219. 92. A REVIEWa
  147220. GABRIEL WEATHERHEAD
  147221. 6293N
  147222. 2/28/96VZSHARPLESS, K. BARRY. COELACANTHS AND CATALYSIS. TETRAHEDRON, 1994,50(15),4235
  147223. 58. A REVIEWa
  147224. GABRIEL WEATHERHEAD
  147225. 6294N
  147226. 2/28/96V
  147227. ANZAI, JUN ICHI; OSA, TETSUO. PHOTOSENSITIVE ARTIFICIAL MEMBRANES BASED ON AZOBENZENE AND SPIROBENZOPYRAN DERIVATIVES. TETRAHEDRON, 1994, 50(14), 4039
  147228. 70. A REVIEWa
  147229. GABRIEL WEATHERHEAD
  147230. 6295N
  147231. 2/28/96V
  147232. KOTHA, SAMBASIVARAO. OPPORTUNITIES IN ASYMMETRIC SYNTHESIS: AN INDUSTRIAL PROSPECT. TETRAHEDRON, 1994, 50(12), 3639
  147233. 62. A REVIEWa
  147234. GABRIEL WEATHERHEAD
  147235. 6296N
  147236. 2/28/96V
  147237. BURTON, DONALD J.; YANG, ZHEN YU; MORKEN, PETER A. FLUORINATED ORGANOMETALLICS: VINYL, ALKYNYL, ALLYL, BENZYL, PROPARGYL AND ARYL FLUORINATED ORGANOMETALLIC REAGENTS IN ORGANIC SYNTHESIS. TETRAHEDRON, 1994, 50(10), 2993
  147238. 3063. A REVIEW
  147239. GABRIEL WEATHERHEAD
  147240. 6297N
  147241. 2/28/96V
  147242. KATRITZKY, ALAN R.; LAN, XIANGFU; FAN, WEI QIANG. BENZOTRIAZOLE AS A SYNTHETIC AUXILIARY: BENZOTRIAZOLYLALKYLATIONS AND BENZOTRIAZOLE
  147243. MEDIATED HETEROALKYLATION. SYNTHESIS, 1994, (5), 445
  147244. 56. A REVIEWa
  147245. GABRIEL WEATHERHEAD
  147246. 6298N
  147247. 2/28/96V
  147248. BONINI, CARLO; RIGHI, GIULIANA. REGIO
  147249.  AND CHEMOSELECTIVE SYNTHESIS OF HALOHYDRINS BY CLEAVAGE OF OXIRANES WITH METAL HALIDES. SYNTHESIS, 1994, (3), 225
  147250. 38. A REVIEWa
  147251. GABRIEL WEATHERHEAD
  147252. 6299N
  147253. 2/28/96V
  147254. BENZ, HERBERT. THE ROLE OF SOLID
  147255. PHASE FRAGMENT CONDENSATION (SPFC) IN PEPTIDE SYNTHESIS. SYNTHESIS, 1994, (4), 337
  147256. 58. A REVIEWa
  147257. GABRIEL WEATHERHEAD
  147258. 6300N
  147259. 2/28/96V
  147260. PRAKASH, OM; SAINI, NEENA; SHARMA, PAWAN K. HYPERVALENT IODINE REAGENTS IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. SYNLETT, 1994, (4), 221
  147261. 7. A REVIEWa
  147262. GABRIEL WEATHERHEAD
  147263. 6301N
  147264. 2/28/96
  147265. !VmCORNELIS, ANDRE; LASZLO, PIERRE. MOLDING CLAYS INTO EFFICIENT CATALYSTS. SYNLETT, 1994, (3), 155
  147266. 61. A REVIEWa
  147267. GABRIEL WEATHERHEAD
  147268. 6302N
  147269. 2/28/96V
  147270. HARADA, TOSHIRO; OKU, AKIRA. ENANTIODIFFERENTIATING TRANSFORMATION OF PROCHIRAL POLYOLS BY USING MENTHONE AS CHIRAL TEMPLATE. SYNLETT, 1994, (2), 95
  147271. 104. A REVIEWa
  147272. GABRIEL WEATHERHEAD
  147273. 6303N
  147274. 2/28/96V
  147275. BRANDUKOVA, N. E.; VYGODSKII, YA. S.; VINOGRADOVA,S. V. THE USE OF SAMARIUM DIIODIDE IN ORGANIC AND POLYMER SYNTHESIS. RUSSIAN CHEMICAL REVIEWS, 1994, 63(4), 345. A REVIEWa
  147276. GABRIEL WEATHERHEAD
  147277. 6304N
  147278. 2/28/96VdKOVAL', I. V. SULFIDES: SYNTHESIS AND PROPERTIES. RUSSIAN CHEMICAL REVIEWS, 1994,63(4),323. A REVIEWa
  147279. GABRIEL WEATHERHEAD
  147280. 6305N
  147281. 2/28/96V
  147282. NAZIN, G. M.; MANELIS, G. B. THERMAL DECOMPOSITION OF ALIPHATIC NITRO COMPOUNDS. RUSSIAN CHEMICAL REVIEWS, 1994, 63(4), 197. A REVIEWa
  147283. GABRIEL WEATHERHEAD
  147284. 6306N
  147285. 2/28/96
  147286. TERENT'EV, A. B.; VASIL'EVA, T. T. THE SYNTHESIS AND REACTIVITY OF ORGANOBROMINE COMPOUNDS IN HOMOLYTIC ADDITION AND TELOMERIZATION PROCESSES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(3), 269. A REVIEWa
  147287. GABRIEL WEATHERHEAD
  147288. 6307N
  147289. 2/28/96V
  147290. GRIGHCHUK, B. D.; GORBOVOI, P. M., GANUSHCHAK, N. I.; DOMBROVSKII, A. V. REACTIONS OF AROMATIC DIAZONIUM SALTS WITH UNSATURATED COMPOUNDS IN THE PRESENCE OF NUCLEOPHILES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(3), 257. A REVIEWa
  147291. GABRIEL WEATHERHEAD
  147292. 6308N
  147293. 2/28/96V
  147294. PUTALA, M.; LEMENOVSKII, D. A. REACTIONS OF DIAZOALKANES WITH TRANSITION METAL COMPLEXES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(3),197. A REVIEWa
  147295. GABRIEL WEATHERHEAD
  147296. 6309N
  147297. 2/28/96V
  147298. GRIGOR'EVA, N. YA.; PINSKER, O. A. NEW METHODS OF SYNTHESIS OF LINEAR FUNCTIONALIZED (Z)
  147299. ISOPRENOIDS AND THEIR 2,3
  147300. DIHYDRO
  147301. DERIVATIVES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(2), 169. A REVIEWa
  147302. GABRIEL WEATHERHEAD
  147303. 6310N
  147304. 2/28/96
  147305. *V{KOVAL', I. V. SULFIDES IN ORGANIC SYNTHESIS. APPLICATIONS OF SULFIDES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(2), 147. A REVIEWa
  147306. GABRIEL WEATHERHEAD
  147307. 6311N
  147308. 2/28/96V
  147309. SHISHKINA, R. P.; BEREZHNAYA, V. N. PHOTOCHEMISTRY OF 2
  147310. DIALKYL AMINO
  147311.  NAPHTHOQUINONES. RUSSIAN CHEMICAL REVIEWS, 1994, 63(2), 139. A REVIEWa
  147312. GABRIEL WEATHERHEAD
  147313. 6312N
  147314. 2/28/96V
  147315. GOL'DSHLEGER, N. F.; MORAVSKII, A. P. REACTIONS OF HYDROCARBONS WITH ELECTROPHILIC TRANSITION METAL COMPLEXES IN TRIFLUOROACETIC ACID. RUSSIAN CHEMICAL REVIEWS, 1994, 63(2), 125. A REVIEWa
  147316. GABRIEL WEATHERHEAD
  147317. 6313N
  147318. 2/28/96V
  147319. NIFANT'EV, E. E.; PREDVODITELEV, D. A. DERIVATIVES OF TRIVALENT PHOSPHORUS IN THE SYNTHESIS OF GLYCEROPHOSPHATIDES AND RELATED PHOSPHOLIPIDS. RUSSIAN CHEMICAL REVIEWS, 1994, 63(1), 71. A REVIEWa
  147320. GABRIEL WEATHERHEAD
  147321. 6314N
  147322. 2/28/96
  147323. JANSEN, R. J. J.; VAN VELDHUIZEN, H. M.; SCHWEGLER, M. A.; VAN BEKKUM, H. RECENT (1987
  147324. 1993) DEVELOPMENTS IN HETEROPOLYACID CATALYSTS IN ACID CATALYZED REACTIONS AND OXIDATION CATALYSIS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147325. BAS, 1994,113(3),115
  147326. 35. A REVIEW
  147327. GABRIEL WEATHERHEAD
  147328. 6315N
  147329. 2/28/96V
  147330. LISKAMP, ROB M. J. CONFORMATIONALLY RESTRICTED AMINO ACIDS AND DIPEPTIDES, (NON)PEPTIDOMIMETICS AND SECONDARY STRUCTURE MIMETICS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147331. BAS, 1994,113(1), 1
  147332. 19. A REVIEWa
  147333. GABRIEL WEATHERHEAD
  147334. 6316N
  147335. 2/28/96V
  147336. KOVACS, LAJOS. METHODS FOR THE SYNTHESIS OF ALPHA
  147337. KETO ESTERS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147338. BAS, 1993,112(9), 471
  147339. 96. A REVIEWa
  147340. GABRIEL WEATHERHEAD
  147341. 6317N
  147342. 2/28/96V
  147343. PANDIT, UPENDRA K. PROGRAMMED ANTIBODIES AS TAILOR
  147344. MADE CATALYSTS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147345. BAS, 1993,112(7
  147346. 8), 431
  147347. 43. A REVIEWa
  147348. GABRIEL WEATHERHEAD
  147349. 6318N
  147350. 2/28/96
  147351. SCHNEIDER, HANS JOERG. SUPRAMOLECULAR CHEMISTRY. 36 NMR SPECTROSCOPY AND MOLECULAR
  147352. MECHANICS CALCULATIONS IN SUPRAMOLECULAR CHEMISTRY. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147353. BAS, 1993,112(6), 412
  147354. 19. A REVIEWa
  147355. GABRIEL WEATHERHEAD
  147356. 6319N
  147357. 2/28/96
  147358. JVAN DEN BROEK, L. A. G. M.; VERMAAS, D. J.; HESKAMP, B. M.; VAN BOECKEL, C. A. A.; TAN, M. C. A. A.; BOLSCHER, J. G. M.; PLOEGH, H. L.; ET AL. CHEMICAL MODIFICATION OF AZA SUGARS, INHIBITORS OF N
  147359. GLYCOPROTEIN
  147360.  PROCESSING GLYCOSIDASES AND OF HIV
  147361. I INFECTION. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  147362. BAS, 1993, 112(2),82
  147363. 94. A REVIEW
  147364. GABRIEL WEATHERHEAD
  147365. 6320N
  147366. 2/28/96V
  147367. JAIN, D. V. S.; DHAR, N. S. THERMODYNAMICS OF BINARY MIXTURES OF ALKYLBENZENES: ROLE OF ORIENTATIONAL ORDER IN BENZENE + ALKYLBENZENE MIXTURES. PURE AND APPLIED CHEMISTRY, 1994, 66(3), 399
  147368. 404. A REVIEWa
  147369. GABRIEL WEATHERHEAD
  147370. 6321N
  147371. 2/28/96
  147372. SUZUKI, AKIRA. NEW SYNTHETIC TRANSFORMATIONS VIA ORGANOBORON COMPOUNDS. PURE AND APPLIED CHEMISTRY, 1994, 66(2), 213
  147373. 22. A REVIEWa
  147374. GABRIEL WEATHERHEAD
  147375. 6322N
  147376. 2/28/96VsPELTER, ANDREW. SOME CHEMISTRY OF HINDERED ORGANOBORANES. PURE AND APPLIED CHEMISTRY, 1994, 66(2), 223
  147377. 33. A REVIEWa
  147378. GABRIEL WEATHERHEAD
  147379. 6323N
  147380. 2/28/96V
  147381. BROWN, HERBERT C.; RAMACHANDRAN, P. V. RECENT ADVANCES IN THE BORON ROUTE TO ASYMMETRIC SYNTHESIS. PURE AND APPLIED CHEMISTRY, 1994,66(2),201
  147382. 12. A REVIEWa
  147383. GABRIEL WEATHERHEAD
  147384. 6324N
  147385. 2/28/96V
  147386. FROMAN, MARK A. THE SYNTHESIS AND REACTIONS OF PRISMANES. RECENT DEVELOPMENTS. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994, 26(3), 291
  147387.  320. A REVIEWa
  147388. GABRIEL WEATHERHEAD
  147389. 6325N
  147390. 2/28/96V
  147391. BERTRAND, MICHELE P. RECENT PROGRESS IN THE USE OF SULFONYL RADICALS IN ORGANIC SYNTHESIS. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994, 26(3), 257
  147392. 90. A REVIEW
  147393. GABRIEL WEATHERHEAD
  147394. 6326N
  147395. 2/28/96V
  147396. ARESTA, MICHELE; QUARANTA, EUGENIO; TOMMASI, IMMACOLATA. THE ROLE OF METAL CENTERS IN REDUCTION AND CARBOXYLATION REACTIONS UTILIZING CARBON DIOXIDE. NEW JOURNAL OF CHEMISTRY, 1994, 18(1),133
  147397. 42. A REVIEWa
  147398. GABRIEL WEATHERHEAD
  147399. 6327N
  147400. 2/28/96V
  147401. WOJCICKI, ANDREW. MONONUCLEAR TRANSITION
  147402. METAL 173
  147403. PROPARGYL/ALLENYL COMPLEXES: SYNTHESIS, STRUCTURE AND REACTION CHEMISTRY. NEW JOURNAL OF CHEMISTRY, 1994,18(1), 61 
  147404. 8. A REVIEWa
  147405. GABRIEL WEATHERHEAD
  147406. 6328N
  147407. 2/28/96V
  147408. OGINO, HIROSHI. THREADING MOLECULAR STRINGS ONTO MOLECULAR RINGS. SYNTHESIS OF ROTAXANES BY USE OF CYCLODEXTRINS. NEW JOURNAL OF CHEMISTRY, 1993,17(10
  147409. 11), 683
  147410. 8. A REVIEWa
  147411. GABRIEL WEATHERHEAD
  147412. 6329N
  147413. 2/28/96VqCONNOLLY, J. D.; HILL, R. A.; NGADJUI, B. T. TRITERPENOIDS. NATURAL PRODUCT REPORTS, 1994,11(1), 91
  147414. 117. A REVIEWa
  147415. GABRIEL WEATHERHEAD
  147416. 6330N
  147417. 2/28/96
  147418. >V^GILL, M. PIGMENTS OF FUNGI (MACROMYCETES). NATURAL PRODUCT REPORTS, 1994,11(1),67
  147419. 90. A REVIEWa
  147420. GABRIEL WEATHERHEAD
  147421. 6331N
  147422. 2/28/96V
  147423. HASLAM, E.; CAI, Y. PLANT POLYPHENOLS (VEGETABLE TANNINS): GALLIC ACID METABOLISM. NATURAL PRODUCT REPORTS, 1994, 11(1), 41
  147424. 66. A REVIEWa
  147425. GABRIEL WEATHERHEAD
  147426. 6332N
  147427. 2/28/96VmMICHAEL, J. P. INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDS. NATURAL PRODUCT REPORTS, 1994,11(1), 17
  147428. 39. A REVIEWa
  147429. GABRIEL WEATHERHEAD
  147430. 6333N
  147431. 2/28/96V
  147432. TURNER, N. J. RECENT ADVANCES IN THE USE OF ENZYME
  147433. CATALYZED REACTIONS IN ORGANIC SYNTHESIS. NATURAL PRODUCT REPORTS, 1994, 11(1),1
  147434. 15 A REVIEWa
  147435. GABRIEL WEATHERHEAD
  147436. 6334N
  147437. 2/28/96V
  147438. CLOUGH, J. M. THE STROBILURINS, OUDEMANSINS AND MYXOTHIAZOLS, FUNGICIDAL DERIVATIVES OF BETA
  147439. METHOXYACRYLIC ACIDS. NATURAL PRODUCT REPORTS, 1993,10(6), 565
  147440. 74. A REVIEWa
  147441. GABRIEL WEATHERHEAD
  147442. 6335N
  147443. 2/28/96
  147444. HIRST, JACK. MECHANISMS OF AROMATIC NUCLEOPHILIC SUBSTITUTION REACTIONS BY AMINES IN SOLVENTS OF LOW RELATIVE PERMITTIVITY. JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1994, 7(2), 68
  147445. 79. A REVIEWa
  147446. GABRIEL WEATHERHEAD
  147447. 6336N
  147448. 2/28/96V
  147449. NAKAGAKI, RYOICHI; TANIMOTO, YOSHIFUMI; MUTAI, KIYOSHI. MAGNETIC FIELD EFFECTS UPON PHOTOCHEMISTRY OF BIFUNCTIONAL CHAIN MOLECULES. JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1993, 6(7), 381
  147450. 92. A REVIEWa
  147451. GABRIEL WEATHERHEAD
  147452. 6337N
  147453. 2/28/96V
  147454. MODERHACK, DIETRICH. OXO
  147455.  AND IMINO
  147456. FUNCTIONALIZED 1,2
  147457. OXAZETIDINES. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30(3), 579
  147458. 91. A REVIEWa
  147459. GABRIEL WEATHERHEAD
  147460. 6338N
  147461. 2/28/96V
  147462. CATSOULACOS, P.; CATSOULACOS, D. FORMATION OF HOMO
  147463. STEROIDS AND DERIVATIVES BY BECKMANN REARRANGEMENT. ANTITUMOR ACTIVITY OF STEREOISOMERS HOMO
  147464. STEROIDAL ESTERS. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30(1), 1
  147465. 10. A REVIEWa
  147466. GABRIEL WEATHERHEAD
  147467. 2/28/96V
  147468. PACIOREK, K. J. L.; KRATZER, R. H. STABILITY OF PERFLUOROALKYLETHERS. JOURNAL OF FLUORINE CHEMISTRY, 1994, 67(2), 169
  147469. 75. A REVIEWa
  147470. GABRIEL WEATHERHEAD
  147471. 6340N
  147472. 2/28/96V
  147473. GERASIMOVA, T. N.; KOLCHINA, E. F. THE SMILES REARRANGEMENT IN THE POLYFLUOROAROMATIC SERIES. JOURNAL OF FLUORINE CHEMISTRY, 1994 66(1), 69
  147474. 74. A REVIEWa
  147475. GABRIEL WEATHERHEAD
  147476. 6341N
  147477. 2/28/96V
  147478. PANDIEWICZ, KRZYSZTOF W., WATANABE, KYOICHI A. SYNTHESIS OF 2'
  147479. FLUORO
  147480. SUBSTITUTED NUCLEOSIDES BY A DIRECT APPROACH. JOURNAL OF FLUORINE CHEMISTRY, 1993, 64(1
  147481. 2), 15
  147482. 36. A REVIEWa
  147483. GABRIEL WEATHERHEAD
  147484. 6342N
  147485. 2/28/96V
  147486. SAWADA, HIDEO. SYNTHESIS OF PERFLUORO
  147487. ALKYLATED COMPOUNDS BY THE USE OF PERFLUORO
  147488. ALKANOYL PEROXIDES AND THEIR APPLICATIONS. JOURNAL OF FLUORINE CHEMISTRY, 1993, 61(3). 253
  147489. 72. A REVIEWa
  147490. GABRIEL WEATHERHEAD
  147491. 6343N
  147492. 2/28/96
  147493. VLASOV, V. M. FLUORIDE ION AS A NUCLEOPHILE AND A LEAVING GROUP IN AROMATIC NUCLEOPHILIC SUBSTITUTION REACTIONS. JOURNAL OF FLUORINE CHEMISTRY, 1993, 61(3), 193
  147494. 216. A REVIEWa
  147495. GABRIEL WEATHERHEAD
  147496. 6344N
  147497. 2/28/96V
  147498. WAKSELMAN, CLAUDE. SINGLE ELECTRON
  147499. TRANSFER PROCESSES IN PERFLUOROALKYL HALIDE REACTIONS. JOURNAL OF FLUORINE CHEMISTRY, 1992, 59(3) 367
  147500. 78. A REVIEWa
  147501. GABRIEL WEATHERHEAD
  147502. 6345N
  147503. 2/28/96V
  147504. HUANG, WEIYUAN. PERFLUOROALKYLATION INITIATED WITH SODIUM DITHIONITE AND RELATED REAGENT SYSTEMS. JOURNAL OF FLUORINE CHEMISTRY, 1992, 58(1), 1
  147505. 8. A REVIEWa
  147506. GABRIEL WEATHERHEAD
  147507. 6346N
  147508. 2/28/96V
  147509. ANDREEV, V. G.; KOLOMIETS, A. F.; FOKIN, A. V. [3,3]
  147510. SIGMATROPIC REARRANGEMENTS OF FLUOROCARBANIONS. JOURNAL OF FLUORINE CHEMISTRY, 1992, 56(3), 259
  147511. 69. A REVIEWa
  147512. GABRIEL WEATHERHEAD
  147513. 6347N
  147514. 2/28/96
  147515. DANELON, GERARDO O.; MASCARETTI, ORESTE A. FLUORINATED PENICILLINS AND OTHER BETA
  147516. LACTAMS: CHEMISTRY AND BIOLOGICAL ACTIVITY. JOURNAL OF FLUORINE CHEMISTRY, 1992, 56(2), 109
  147517. 40. A REVIEWa
  147518. GABRIEL WEATHERHEAD
  147519. 6348N
  147520. 2/28/96V
  147521. JOSHI, KRISHNA C.; JAIN, RENUKA; DANDIA, ANSHU SHARMA, KANTI. FLUORINE
  147522. CONTAINING BIOACTIVE BENZIMIDAZOLES. JOURNAL OF FLUORINE CHEMISTRY, 1992, 56(1), 1
  147523. 27. A REVIEWa
  147524. GABRIEL WEATHERHEAD
  147525. 6349N
  147526. 2/28/96V
  147527. YOSHIDA, MASATO; KAMIGATA, NOBUMASA. RECENT PROGRESS IN PERFLUOROALKYLATION BY RADICAL SPECIES WITH SPECIAL REFERENCE TO THE USE OF BIS(PERFLUOROALKANOYL) PEROXIDES. JOURNAL OF FLUORINE CHEMISTRY, 1990, 49(1), 1
  147528. 20. A REVIEWa
  147529. GABRIEL WEATHERHEAD
  147530. 6350N
  147531. 2/28/96V
  147532. RODIONOV, P. P.; FURIN, G. G. KINETICS OF NUCLEOPHILIC SUBSTITUTION REACTIONS OF POLYFLUOROAROMATIC COMPOUNDS. JOURNAL OF FLUORINE CHEMISTRY, 1990, 47(3), 361
  147533. 434. A REVIEWa
  147534. GABRIEL WEATHERHEAD
  147535. 6351N
  147536. 2/28/96
  147537. KOBRINA, L. S. SOME PECULIARITIES OF RADICAL REACTIONS OF POLYFLUOROAROMATIC COMPOUNDS. JOURNAL OF FLUORINE CHEMISTRY, 1989, 42(3) 301 
  147538. 44. A REVIEWa
  147539. GABRIEL WEATHERHEAD
  147540. 6352N
  147541. 2/28/96V
  147542. JARMAN, M. PERFLUOROARENES AS NOVEL AND SELECTIVE PROTECTING REAGENTS; APPLICATIONS IN ANTICANCER DRUG DEVELOPMENT. JOURNAL OF FLUORINE CHEMISTRY, 1989, 42(1), 3
  147543. 15. A REVIEWa
  147544. GABRIEL WEATHERHEAD
  147545. 6353N
  147546. 2/28/96VgGROMOV, SERGEI P.; KOST, ALEKSEI N. ENAMINE REARRANGEMENT. HETEROCYCLES, 1994, 38(5), 1127
  147547. 55. A REVIEWa
  147548. GABRIEL WEATHERHEAD
  147549. 6354N
  147550. 2/28/96VtSLIWA, WANDA. THE REACTIVITY OF ACRIDINIUM SALTS AND RELATED COMPOUNDS. HETEROCYCLES, 1994, 38(4), 897
  147551. 922. A REVIEWa
  147552. GABRIEL WEATHERHEAD
  147553. 6355N
  147554. 2/28/96V
  147555. PRAKASH, O. M., SAINI, NEENA, SHARMA, PAWAN. [HYDROXY(TOSYLOXY) IODO]BENZENE: A USEFUL HYPERVALENT IODINE REAGENT FOR THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. HETEROCYCLES, 1994, 38(2), 409
  147556. 31. A REVIEW
  147557. GABRIEL WEATHERHEAD
  147558. 6356N
  147559. 2/28/96VaANDO, KAORI; TAKAYAMA, HIROAKI. HETEROAROMATIC FUSED 3
  147560. SULFOLENES. 1994, 37(2), 1417
  147561. 39. A REVIEWa
  147562. GABRIEL WEATHERHEAD
  147563. 6357N
  147564. 2/28/96V
  147565. BREWSTER, MARCUS E.; POP, EMIL; HUANG, MING JU; BODOR, NICHOLAS. CONTRIBUTIONS OF MOLECULAR ORBITAL TECHNIQUES TO THE STUDY OF DIHYDROPYRIDINES. HETEROCYCLES, 1994, 37(2) 1373
  147566. 415. A REVIEWa
  147567. GABRIEL WEATHERHEAD
  147568. 6358N
  147569. 2/28/96VhOAE, SHIGERU. SMALL RING COMPOUNDS CONTAINING SULFUR ATOMS. HETEROCYCLES, 1994, 37(2), 1359
  147570. 71. A REVIEWa
  147571. GABRIEL WEATHERHEAD
  147572. 6359N
  147573. 2/28/96VZKUTHAN, JOSEF. EXTENSION OF DECKER OXIDATION. HETEROCYCLES, 1994, 37(2), 1347
  147574. 57. A REVIEWa
  147575. GABRIEL WEATHERHEAD
  147576. 6360N
  147577. 2/28/96V
  147578. IDDON, BRIAN. SYNTHESIS AND REACTIONS OF LITHIATED MONOCYCLIC AZOLES CONTAINING TWO OR MORE HETEROATOMS. PART II: OXAZOLES. HETEROCYCLES, 1994, 37(2), 1321
  147579. 46. A REVIEWa
  147580. GABRIEL WEATHERHEAD
  147581. 6361N
  147582. 2/28/96V
  147583. IDDON, BRIAN. SYNTHESIS AND REACTIONS OF LITHIATED MONOCYCLIC AZOLES CONTAINING TWO OR MORE HETEROATOMS. PART I: ISOXAZOLES. HETEROCYCLES, 1994, 37(2), 1263
  147584. 320. A REVIEWa
  147585. GABRIEL WEATHERHEAD
  147586. 6362N
  147587. 2/28/96ViHUANG, ZHITANG; WANG, MEIXIANG. HETEROCYCLIC KETENE AMINALS. HETEROCYCLES, 1994, 37(2), 1233
  147588. 62. A REVIEWa
  147589. GABRIEL WEATHERHEAD
  147590. 6363N
  147591. 2/28/96V
  147592. TROFIMOV, BORIS A.; MIKHALEVA, AL'BINA I. FURTHER DEVELOPMENT OF THE KETOXIME
  147593. BASED PYRROLE SYNTHESIS. HETEROCYCLES, 1994, 37(2), 1193
  147594. 232. A REVIEWa
  147595. GABRIEL WEATHERHEAD
  147596. 6364N
  147597. 2/28/96V
  147598. FARCASIU, DAN; BALABAN, ALEXANDRU T.; BOLOGNA, URSULA L. ONE
  147599. ELECTRON TRANSFER REACTIONS OF PYRYLIUM CATIONS. HETEROCYCLES, 1994, 37(2), 1165
  147600. 92. A REVIEWa
  147601. GABRIEL WEATHERHEAD
  147602. 6365N
  147603. 2/28/96VlKNIGHT, D. W. SYNTHETIC APPROACHES TO BUTENOLIDES. CONTEMPORARY ORGANIC SYNTHESIS, 1994, 1(4), 287. A REVIEWa
  147604. GABRIEL WEATHERHEAD
  147605. 6366N
  147606. 2/28/96V
  147607. KILBURN, JEREMY, D., PATEL, HITESH K. SYNTHETIC DEVELOPMENTS IN HOST
  147608. GUEST CHEMISTRY. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(4), 259. A REVIEWa
  147609. GABRIEL WEATHERHEAD
  147610. 6367N
  147611. 2/28/96VgSWEENEY, JOSEPH. ALCOHOLS, PHENOLS, AND ETHERS. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(4),243. A REVIEWa
  147612. GABRIEL WEATHERHEAD
  147613. 6368N
  147614. 2/28/96V
  147615. MOTHERWELL, W. B., NUTLEY, C. J. THE ROLE OF ZINC CARBENOIDS IN ORGANIC SYNTHESIS. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(4), 219. A REVIEWa
  147616. GABRIEL WEATHERHEAD
  147617. 6369N
  147618. 2/28/96V
  147619. GILCHRIST, THOMAS L. SYNTHESIS OF FIVE
  147620. MEMBERED AROMATIC HETEROCYCLES. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(3), 205. A REVIEWa
  147621. GABRIEL WEATHERHEAD
  147622. 6370N
  147623. 2/28/96V{RAYNER, CHRISTOPHER M. THIOLS, SULFIDES, SULFOXIDES, AND SULFONES. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(3), 191. A REVIEWa
  147624. GABRIEL WEATHERHEAD
  147625. 6371N
  147626. 2/28/96
  147627. gVsCOUSINS, R. P. C. SATURATED AND UNSATURATED HYDROCARBONS. CONTEMPORARY ORGANIC SYNTHESIS, 1994, 1(3), 173. A REVIEWa
  147628. GABRIEL WEATHERHEAD
  147629. 6372N
  147630. 2/28/96V
  147631. GRIBBLE, GORDON W. RECENT DEVELOPMENTS IN INDOLE RING SYNTHESIS
  147632. METHODOLOGY AND APPLICATIONS. CONTEMPORARY ORGANIC SYNTHESIS, 1994, 1(3),145. A REVIEWa
  147633. GABRIEL WEATHERHEAD
  147634. 6373N
  147635. 2/28/96V
  147636. BLAGG, JULIAN. STOICHIOMETRIC APPLICATIONS OF ORGANOTRANSITION METAL COMPLEXES IN ORGANIC SYNTHESIS. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(2),125. A REVIEWa
  147637. GABRIEL WEATHERHEAD
  147638. 6374N
  147639. 2/28/96VXSPARGO, P. L. ORGANIC HALIDES. CONTEMPORARY ORGANIC SYNTHESIS, 1994, 1(2), 113. A REVIEWa
  147640. GABRIEL WEATHERHEAD
  147641. 6375N
  147642. 2/28/96VfSTEELE, JOHN. SATURATED NITROGEN HETEROCYCLES. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(2), 95. A REVIEWa
  147643. GABRIEL WEATHERHEAD
  147644. 6376N
  147645. 2/28/96
  147646. DAWSON, GRAHAM J.; WILLIAMS, JONATHAN M. J. CATALYTIC APPLICATIONS OF TRANSITION METALS IN ORGANIC : SYNTHESIS. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(2), 77. A REVIEWa
  147647. GABRIEL WEATHERHEAD
  147648. 6377N
  147649. 2/28/96V
  147650. BOA, A. N., JENKINS, P. R.; LAWRENCE, N. J. RECENT PROGRESS IN THE SYNTHESIS OF TAXANES. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(1), 47. A REVIEWa
  147651. GABRIEL WEATHERHEAD
  147652. 6378N
  147653. 2/28/96VzMASCAL, MARK. NONCOVALENT DESIGN PRINCIPLES AND THE NEW SYNTHESIS. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(1), 31. A REVIEWa
  147654. GABRIEL WEATHERHEAD
  147655. 6379N
  147656. 2/28/96VpBURNS, CHRISTOPHER, J. SATURATED OXYGEN HETEROCYCLES . CONTEMPORARY ORGANIC SYNTHESIS, 1994, 1 (1), 23. A REVIEWa
  147657. GABRIEL WEATHERHEAD
  147658. 6380N
  147659. 2/28/96V`STEEL, PATRICK, G. ALDEHYDES AND KETONES. CONTEMPORARY ORGANIC SYNTHESIS, 1994,1(1), 1. A REVIEWa
  147660. GABRIEL WEATHERHEAD
  147661. 6381N
  147662. 2/28/96
  147663. PONNAMPERUMA, CYRIL, MACDERMOTT, ALEXANDRA J. COSMIC ASYMMETRY: THE MEANING OF LIFE. CHEMISTRY IN BRITAIN, 1994, 30(6), 384
  147664. 6. A REVIEWa
  147665. GABRIEL WEATHERHEAD
  147666. 6382N
  147667. 2/28/96V^DIAS, JERRY RAY. SETTING BENZENOIDS TO ORDER. CHEMISTRY IN BRITAIN, 1994,30(5),384
  147668. 6. A REVIEWa
  147669. GABRIEL WEATHERHEAD
  147670. 6383N
  147671. 2/28/96VzCAMILLERI, PATRICK; DE BIASI, VERN; HUTT, ANDREW. RESOLVING THE PROBLEM. CHEMISTRY IN BRITAIN, 1994, 30(1), 43
  147672. 6. A REVIEWa
  147673. GABRIEL WEATHERHEAD
  147674. 6384N
  147675. 2/28/96VfNICOLAOU, KYRIACOS. THE MAGIC OF ENEDIYNE CHEMISTRY. CHEMISTRY IN BRITAIN, 1994, 30(1), 33
  147676. 6. A REVIEWa
  147677. GABRIEL WEATHERHEAD
  147678. 6385N
  147679. 2/28/96V_CAREY, JOE. NEW RESOLUTIONS IN DRUG DESIGN. CHEMISTRY IN BRITAIN, 1993, 29(12),1053
  147680. 6. A REVIEWa
  147681. GABRIEL WEATHERHEAD
  147682. 6386N
  147683. 2/28/96V
  147684. JACKSON, ARTHUR; ANGOH, GAE. SMALL MOLECULE, BIG POTENTIAL (OXALYL CHLORIDE). CHEMISTRY IN BRITAIN, 1993, 29(12), 1046
  147685. 648. A REVIEW
  147686. GABRIEL WEATHERHEAD
  147687. 6387N
  147688. 2/28/96VyBRAITHWAITE, NALCOLM; KETTEMAN, CLARE L. TAKING OUT THE TRASH. CHEMISTRY IN BRITAIN, 1993, 29(12),1042
  147689. 44, 1048. A REVIEWa
  147690. GABRIEL WEATHERHEAD
  147691. 6388N
  147692. 2/28/96VUKEELER, JAMES. KNOWING THE UNKNOWN. CHEMISTRY IN BRITAIN, 1993, 29(7),593
  147693. 5. A REVIEWa
  147694. GABRIEL WEATHERHEAD
  147695. 6389N
  147696. 2/28/96VdSMITH, DIANE R. SUPRAMOLECULAR CHEMISTRY. CHEMISTRY AND INDUSTRY (LONDON), 1994, (1),14
  147697. 17. A REVIEWa
  147698. GABRIEL WEATHERHEAD
  147699. 6390N
  147700. 2/28/96V
  147701. NIXON, JOHN F. THE FASCINATING ORGANOMETALLIC CHEMISTRY OF PHOSPHAALKYNES. CHEMISTRY AND INDUSTRY (LONDON), 1993, (11), 404
  147702. 7. A REVIEWa
  147703. GABRIEL WEATHERHEAD
  147704. 6391N
  147705. 2/28/96VzSHELDON, ROGER A. ORGANIC SYNTHESIS
  147706. PAST, PRESENT AND FUTURE. CHEMISTRY AND INDUSTRY (LONDON), 1992, 23, 903
  147707. 906. A REVIEWa
  147708. GABRIEL WEATHERHEAD
  147709. 6392N
  147710. 2/28/96
  147711. RAMSDEN, CHRISTOPHER A. NON
  147712. BONDING MOLECULAR ORBITALS AND THE CHEMISTRY OF NON
  147713. CLASSICAL ORGANIC MOLECULES. CHEMICAL SOCIETY REVIEWS, 1994, 23(2), 111
  147714. 18. A REVIEWa
  147715. GABRIEL WEATHERHEAD
  147716. 6393N
  147717. 2/28/96V
  147718. HUNTER, CHRISTOPHER A. THE ROLE OF AROMATIC INTERACTIONS IN MOLECULAR RECOGNITION. CHEMICAL SOCIETY REVIEWS, 1994, 23(2),101
  147719. 9. A REVIEWa
  147720. GABRIEL WEATHERHEAD
  147721. 6394N
  147722. 2/28/96VsWILLIAMS, A. THE DIAGNOSIS OF CONCERTED ORGANIC MECHANISMS. CHEMICAL SOCIETY REVIEWS, 1994, 23(2), 93
  147723. 100. A REVIEWa
  147724. GABRIEL WEATHERHEAD
  147725. 6395N
  147726. 2/28/96V
  147727. VISSER, HERMAN C.; REINHOUDT, DAVID N.; DE JONG, FEIKE. CARRIER
  147728. MEDIATED TRANSPORT THROUGH LIQUID MEMBRANES. CHEMICAL SOCIETY REVIEWS, 1994, 23(2), 75
  147729. 81. A REVIEWa
  147730. GABRIEL WEATHERHEAD
  147731. 6396N
  147732. 2/28/96
  147733. JORGENSEN, TINE, HANSEN, THOMAS KRUSE; BECHER, JAN . TETRATHIAFULVALENES AS BUILDING
  147734. BLOCKS IN SUPRAMOLECULAR CHEMISTRY. CHEMICAL SOCIETY REVIEWS, 1994, 23(1), 41
  147735. 51. A REVIEWa
  147736. GABRIEL WEATHERHEAD
  147737. 6397N
  147738. 2/28/96V
  147739. AAKEROY, CHRISTER B.; SEDDON, KENNETH R. THE HYDROGEN BOND AND CRYSTAL ENGINEERING. CHEMICAL SOCIETY REVIEWS, 1993, 22(6), 397
  147740. 407. A REVIEWa
  147741. GABRIEL WEATHERHEAD
  147742. 6398N
  147743. 2/28/96V
  147744. YE, TAO, MCKERVEY, M. ANTHONY. ORGANIC SYNTHESIS WITH A
  147745. DIAZO CARBONYL COMPOUNDS. CHEMICAL REVIEWS, 1994, 94(4), 1091
  147746. 160. A REVIEWa
  147747. GABRIEL WEATHERHEAD
  147748. 6399N
  147749. 2/28/96V
  147750. MIRANDA MIGUEL A.; GARCIA, HERMENEGILDO. 2,4,6
  147751. TRIPHENYLPYRYLIUM TETRAFLUOROBORATE AS AN ELECTRON TRANSFER PHOTOSENSITIZER. CHEMICAL REVIEWS, 1994, 94(4), 1063
  147752. 89. A REVIEWa
  147753. GABRIEL WEATHERHEAD
  147754. 6400N
  147755. 2/28/96
  147756. GRUSHIN, VLADIMIR V., ALPER, HOWARD. TRANSFORMATIONS OF CHLOROARENES, CATALYZED BY TRANSITION
  147757. METAL COMPLEXES. CHEMICAL REVIEWS, 1994, 94(4), 1047
  147758. 62. A REVIEWa
  147759. GABRIEL WEATHERHEAD
  147760. 6401N
  147761. 2/28/96V
  147762. AN, HAOYUN; BRADSHAW, JERALD S.; IZATT, REED M.; YAN, ZHENGMING. BIS
  147763.  AND OLIGO(BENZOCROWN ETHER)S. CHEMICAL REVIEWS, 1994,94(4),939
  147764. 91. A REVIEWa
  147765. GABRIEL WEATHERHEAD
  147766. 6402N
  147767. 2/28/96VzWALDMANN, HERBERT; SEBASTIAN, DAGMAR. ENZYMIC PROTECTING GROUP TECHNIQUES. CHEMICAL REVIEWS, 1994, 94(4), 911
  147768. 37. A REVIEWa
  147769. GABRIEL WEATHERHEAD
  147770. 6403N
  147771. 2/28/96V
  147772. GILGE, JOHN W.; ROESKY, HERBERT W. STRUCTURALLY CHARACTERIZED ORGANOMETALLIC HYDROXO COMPLEXES OF THE F
  147773.  AND D
  147774. BLOCK METALS. CHEMICAL REVIEWS, 1994, 94(4), 895
  147775. 910 . A REVIEWa
  147776. GABRIEL WEATHERHEAD
  147777. 6404N
  147778. 2/28/96V
  147779. RAJCA, ANDRZEJ. ORGANIC DIRADICALS AND POLYRADICALS: FROM SPIN COUPLING TO MAGNETISM? CHEMICAL REVIEWS, 1994, 94(4),871
  147780. 93. A REVIEW
  147781. GABRIEL WEATHERHEAD
  147782. 6405N
  147783. 2/28/96V
  147784. NESPER, REINHARD. FULLERCAGES WITHOUT CAR BON
  147785. FULLERANES, FULLERENES, SPACE
  147786. FILLER
  147787. ENES? ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(8), 843
  147788. 6. A REVIEWa
  147789. GABRIEL WEATHERHEAD
  147790. 6406N
  147791. 2/28/96V
  147792. WENZ, GERHARD. CYCLODEXTRINS AS BUILDING BLOCKS FOR SUPRAMOLECULAR STRUCTURES AND FUNCTIONAL UNITS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994,33(8),803
  147793. 22. A REVIEWa
  147794. GABRIEL WEATHERHEAD
  147795. 6407N
  147796. 2/28/96V
  147797. KAUPP, GERHARD. RESOLUTION OF RACEMATES BY DISTILLATION WITH INCLUSION COMPOUNDS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(7), 728
  147798. 9. A REVIEWa
  147799. GABRIEL WEATHERHEAD
  147800. 6408N
  147801. 2/28/96V
  147802. METZGER, JORG W. LADDER SEQUENCING OF PEPTIDES AND PROTEINS
  147803. A COMBINATION OF EDMAN DEGRADATION AND MASS SPECTROMETRY. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(7), 723
  147804. 5. A REVIEWa
  147805. GABRIEL WEATHERHEAD
  147806. 6409N
  147807. 2/28/96V
  147808. STEC, WOJCIECH J.; WILK, ANDRZEJ. STEREOCONTROLLED SYNTHESIS OF OLIGO(NUCLEOSIDE PHOSPHOROTHIOATE)S. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(7),709
  147809. 22. A REVIEWa
  147810. GABRIEL WEATHERHEAD
  147811. 6410N
  147812. 2/28/96V
  147813. BUTENSCHON, HOLGER. CONSTRUCTION OF CARBON FRAME WORKS WITH THE HELP OF RUTHENIUM COMPLEXES: 1,5
  147814. CYCLOOCTADIENE AS REACTANT IN TRANSITION METAL CATALYZED REACTIONS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(6), 636
  147815. 8. A REVIEWa
  147816. GABRIEL WEATHERHEAD
  147817. 6411N
  147818. 2/28/96V
  147819. TANNER, DAVID. CHIRAL AZIRIDINES. THEIR SYNTHESIS AND USE IN STEREOSELECTIVE TRANSFORMATIONS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(6), 599
  147820. 619. A REVIEWa
  147821. GABRIEL WEATHERHEAD
  147822. 6412N
  147823. 2/28/96VsKIRBY, ANTHONY J. ENZYME MIMICS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(5), 551
  147824. 53. A REVIEWa
  147825. GABRIEL WEATHERHEAD
  147826. 6413N
  147827. 2/28/96
  147828. LANG, HEINRICH. NOVEL CARBON COMPOUNDS WITH "NAKED" CN UNITS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(5), 547
  147829. 50. A REVIEWa
  147830. GABRIEL WEATHERHEAD
  147831. 6414N
  147832. 2/28/96V
  147833. BERTRAND, GUY; WENTRUP, CURT. NITRILE IMINES: FROM MATRIX CHARACTERIZATION TO STABLE COMPOUNDS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994 33(5), 527
  147834. 45. A REVIEWa
  147835. GABRIEL WEATHERHEAD
  147836. 6415N
  147837. 2/28/96V
  147838. TOGNI, ANTONIO; VENANZI, LUIGI M. NITROGEN DONORS IN ORGANOMETALLIC CHEMISTRY AND HOMOGENEOUS CATALYSIS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(5), 497
  147839. 526. A REVIEWa
  147840. GABRIEL WEATHERHEAD
  147841. 6416N
  147842. 2/28/96V
  147843. LAATSCH, HARTMUT. CONOCURVONE
  147844. PROTOTYPE OF A NEW CLASS OF ANTI
  147845. HIV ACTIVE COMPOUND? ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(4), 422
  147846. 4. A REVIEWa
  147847. GABRIEL WEATHERHEAD
  147848. 6417N
  147849. 2/28/96
  147850. GIANNIS, ATHANASSIOS. THE SIALYL LEWIS
  147851. X GROUP AND ITS ANALOGS AS LIGANDS FOR SELECTINS: CHEMOENZYMATIC SYNTHESES AND BIOLOGICAL FUNCTIONS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH, 1994, 33(2),178
  147852. 80. A REVIEWa
  147853. GABRIEL WEATHERHEAD
  147854. 6418N
  147855. 2/28/96VvWILLIAMS, RICHARD V.; KURTZ, HENRY A. HOMOAROMATICITY. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY, 1994, 29, 273. A REVIEWa
  147856. GABRIEL WEATHERHEAD
  147857. 6419N
  147858. 2/28/96V
  147859. KOCHI, JAY K. ELECTRON TRANSFER IN THE THERMAL AND PHOTOCHEMICAL ACTIVATION OF ELECTRON DONOR
  147860. ACCEPTOR COMPLEXES IN ORGANIC AND ORGANOMETALLIC REACTIONS. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY, 1994 29, 185. A REVIEWa
  147861. GABRIEL WEATHERHEAD
  147862. 6420N
  147863. 2/28/96V
  147864. KIRBY, ANTHONY J. CRYSTALLOGRAPHIC APPROACHES TO TRANSITION STATE STRUCTURES. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY, 1994, 29, 87. A REVIEWa
  147865. GABRIEL WEATHERHEAD
  147866. 6421N
  147867. 2/28/96
  147868. TEE, OSWALD S. THE STABILIZATION OF TRANSITION STATES BY CYCLODEXTRINS AND OTHER CATALYSTS. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY, 1994, 29,1. A REVIEWa
  147869. GABRIEL WEATHERHEAD
  147870. 6422N
  147871. 2/28/96V
  147872. SCHAVERIEN, COLIN J. ORGANOMETALLIC CHEMISTRY OF THE LANTHANIDES. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 283. A REVIEWa
  147873. GABRIEL WEATHERHEAD
  147874. 6423N
  147875. 2/28/96V
  147876. ZYBILL, CHRISTIAN; HANDWERKER, HERMANN; FRIEDRICH, HOLGER. SILAORGANOMETALLIC CHEMISTRY ON THE BASIS OF MULTIPLE BONDING. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 229. A REVIEWa
  147877. GABRIEL WEATHERHEAD
  147878. 6424N
  147879. 2/28/96V
  147880. HILL, ANTHONY F. ORGANOTRANSITION METALLIC CHEMISTRY OF SULFUR DIOXIDE ANALOGS. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 159. A REVIEWa
  147881. GABRIEL WEATHERHEAD
  147882. 6425N
  147883. 2/28/96
  147884. WHITE, DAVID; COVILLE, NEIL J. QUANTIFICATION OF STERIC EFFECTS IN ORGANOMETALLIC CHEMISTRY. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 95. A REVIEWa
  147885. GABRIEL WEATHERHEAD
  147886. 6426N
  147887. 2/28/96VtBOWSER, J. R. ORGANOMETALLIC DERIVATIVES OF FULLERENES. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 57. A REVIEWa
  147888. GABRIEL WEATHERHEAD
  147889. 6427N
  147890. 2/28/96V}WILLIAMS, ROBERT E. EARLY CARBORANES AND THEIR STRUCTURAL LEGACY. ADVANCES IN ORGANOMETALLIC CHEMISTRY, 1994, 36, 1. A REVIEWa
  147891. GABRIEL WEATHERHEAD
  147892. 6428N
  147893. 2/28/96V
  147894. GRIMMETT, M. ROSS. HALOGENATION OF HETEROCYCLES: III. HETEROCYCLES FUSED TO OTHER AROMATIC OR HETEROAROMATIC RINGS. ADVANCES IN HETEROCYCLIC CHEMISTRY, 1994, 59, 246. A REVIEWa
  147895. GABRIEL WEATHERHEAD
  147896. 6429N
  147897. 2/28/96V
  147898. KUTHAN, J.; SEBEK, P.; BOHM, S. DEVELOPMENTS IN THE CHEMISTRY OF THIOPYRANS, SELENOPYRANS, AND TELUROPYRANS. ADVANCES IN HETEROCYCLIC CHEMISTRY, 1994, 59, 180. A REVIEW
  147899. GABRIEL WEATHERHEAD
  147900. 6430N
  147901. 2/28/96V
  147902. EL ASHRY, E. S. H.; RASHED, N.; TAHA, M.; RAMADAN, E. CONDENSED 1,2,4
  147903. TRIAZINES: I. FUSED TO HETEROCYCLES WITH THREE
  147904. , FOUR
  147905. , AND FIVE
  147906. MEMBERED RINGS. ADVANCES IN HETEROCYCLIC CHEMISTRY, 1994, 59, 41. A REVIEWa
  147907. GABRIEL WEATHERHEAD
  147908. 6431N
  147909. 2/28/96V
  147910. SILVESTER, MICHAEL J. RECENT ADVANCES IN FLUORO
  147911. HETEROCYCLIC CHEMISTRY. ADVANCES IN HETEROCYCLIC CHEMISTRY, 1994, 59, 1. A REVIEWa
  147912. GABRIEL WEATHERHEAD
  147913. 6432N
  147914. 2/28/96V
  147915. ZHOU, WEI
  147916. SHAN; XU, XING
  147917. XIANG. TOTAL SYNTHESIS OF THE ANTIMALARIAL SESQUITERPENE PEROXIDE QINGHAOSU AND YINGZHAOSU A. ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27(7), 211
  147918. 16. A REVIEWa
  147919. GABRIEL WEATHERHEAD
  147920. 6433N
  147921. 2/28/96V
  147922. WINTNER, EDWARD A.; CONN, M. MORGAN; REBEK, JULIUS, JR. STUDIES IN MOLECULAR RECOGNITION. ACCOUNTS OF CHEMICAL RESEARCH, 1994 27(7), 198
  147923. 210. A REVIEWa
  147924. GABRIEL WEATHERHEAD
  147925. 6434N
  147926. 2/28/96
  147927. SITA, LAWRENCE R. HEAVY
  147928. METAL ORGANIC CHEMISTRY: BUILDING WITH TIN. ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27(7), 191
  147929. 7. A REVIEWa
  147930. GABRIEL WEATHERHEAD
  147931. 6435N
  147932. 2/28/96V
  147933. LIFSHITZ, CHAVA. TROPYLIUM ION FORMATION FROM TOLUENE: SOLUTION OF AN OLD PROBLEM IN ORGANIC MASS SPECTROMETRY. ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27(5), 138
  147934. 44. A REVIEWa
  147935. GABRIEL WEATHERHEAD
  147936. 6436N
  147937. 2/28/96V
  147938. NEGISHI, EI
  147939. ICHI; TAKAHASHI, TAMOTSU. PATTERNS OF STOICHIOMETRIC AND CATALYTIC REACTIONS OF ORGANOZIRCONIUM AND RELATED COMPLEXES OF SYNTHETIC INTEREST. ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27(5), 124
  147940. 30. A REVIEWa
  147941. GABRIEL WEATHERHEAD
  147942. Tet. Lett.C|SHEA DIELS
  147943. ALDER ENANTIOSELECTIVITY REVIEW INTRODUCTION TETHER REGIOCHEM SILICON CHIRALITY ENANTIOSELECTIVITY INTRAMOLECULARM
  147944. 6437N
  147945. 2/28/96VjROLE OF CHIRAL AUXILIARIES IN TYPE 2 INTRAMOLECULAR DIELS
  147946. ALDER REACTION INFLUENCE ON DIASTEREOSELECTIVITYW
  147947. 1994 P 7311a
  147948. GABRIEL WEATHERHEAD
  147949. SYNLETTCkMOODY REVIEW CARBAZOLE ALKALOID PYRONE DIELS
  147950. ALDER RETROSYNTHETIC COURSE ELLIPTICINE TARGET WRITING STUDENTM
  147951. 6438N
  147952. 2/28/96V SYNTHESIS OF CARBAZOLE ALKALOIDSW
  147953. 1994 P 681a
  147954. GABRIEL WEATHERHEAD
  147955. B    SYNTHESISCmPIANCATELLI COURSE FURAN HETEROCYCLE REVIEW HYDROLYSIS RING OPENING CYCLOPENTENONE DICARBONYL DIAZO OXIDATIONM
  147956. 6439N
  147957. 2/28/96VESYNTHESIS OF 1,4
  147958. DICARBONYL COMPOUNDS AND CYCLOPENTENONES FROM FURANSW
  147959. 1994 P 867a
  147960. GABRIEL WEATHERHEAD
  147961. B    SYNTHESISCsLUBINEAU WATER SOLVENT HYDROPHOBIC EFFECT AQUEOUS MEDIUM RATE ACCELERATION DIELS
  147962. ALDER DIPOLAR
  147963. CYCLOADDITION REVIEWM
  147964. 6440N
  147965. 2/28/96V WATER PROMOTED ORGANIC REACTIONSW
  147966. 1994 P 741a
  147967. GABRIEL WEATHERHEAD
  147968. ORG PREP PROCEDURE INTC
  147969. ZHU QCM
  147970. 6441N
  147971. 2/28/96V@ASYMMETRIC REDUCTIONS OF CARBON
  147972. NITROGEN DOUBLE BONDS 
  147973.  A REVIEWW
  147974. 1994 APRX
  147975.  26(2)a
  147976. GABRIEL WEATHERHEAD
  147977. ORG PREP PROCEDURE INTC
  147978. KOTALI AM
  147979. 6442N
  147980. 2/28/96
  147981. HYDROXYARYL KETONES IN ORGANIC SYNTHESIS 
  147982.  A REVIEWW
  147983. 1994 APRX
  147984.  26(2)a
  147985. GABRIEL WEATHERHEAD
  147986. ORG PREP PROCEDURE INTC
  147987. OH TM
  147988. 6443N
  147989. 2/28/96V>REAGENT
  147990. CONTROLLED ASYMMETRIC DIELS
  147991. ALDER REACTIONS 
  147992.  A REVIEWW
  147993. 1994 APRX
  147994.  26(2)a
  147995. GABRIEL WEATHERHEAD
  147996. J ORG CHEMCHRUANO DIELS
  147997. ALDER ASYMMETRIC REVIEW SULFOXIDE LEWIS ACID 2,3
  147998. SIGMATROPICM
  147999. 6445N
  148000. 2/28/96V
  148001. FIRST DIELS
  148002. ALDER REACTIONS OF ENANTIOMERICALLY PURE 1
  148003. TOLYLSULFINYL DIENES.  STRAIGHTFORWARD ACCESS TO CYCLOHEXENOLS THROUGH TANDEM CYCLOADDITION 2,3
  148004. SIGMATROPIC REARRANGEMENTW
  148005. VOL 59 1994 P 3421a
  148006. GABRIEL WEATHERHEAD
  148007. ORG. PREP. PROC. INTCKBERTRAND, M. P.; ALKENE, RADICAL, SULFONE, CYCLIZATION, LACTAM, PYRROLIDINEM
  148008. 6446N
  148009. 2/28/96VORECENT PROGRESS IN THE USE OF SULFONYL RADICALS IN ORGANIC SYNTHESIS.  A REVIEWW
  148010. 1994 26 259
  148011. GABRIEL WEATHERHEAD
  148012. ADV. HETEROCYCL. CHEM
  148013. CVESKER, J. L.; NEWCOMB, M.; RADICAL, NITROGEN, AMINYL, CYCLIZATION, PYRROLIDINE, REVIEWM
  148014. 6447N
  148015. 2/28/96VjTHE GENERATION OF NITROGEN RADICALS AND THEIR CYCLIZATIONS FOR THE CONSTRUCTION OF THE PYRROLIDINE NUCLEUSW
  148016. 1993 58 1
  148017. GABRIEL WEATHERHEAD
  148018. NAT. PROD. REPORTSC8LEWIS, J.R.; REVIEW, AMARYLLIDACEAE, SCELETIUM ALKALOIDSM
  148019. 6448N
  148020. 2/28/96V&AMARYLLIDACEAE AND SCELETIUM ALKALOIDSW
  148021. 1993 10 291
  148022. GABRIEL WEATHERHEAD
  148023. ACCTS. CHEM. RESCFJOHNSON, C.D.; REVIEW, BALDWIN'S RULES, STEREOELECTRONIC, RING CLOSUREM
  148024. 6449N
  148025. 2/28/96VbSTEREOELECTRONIC EFFECTS IN THE FORMATION OF 5
  148026.  AND 6
  148027. MEMBERED RINGS:  THE ROLE OF BALDWIN'S RULESW
  148028. 1993 26 476
  148029. GABRIEL WEATHERHEAD
  148030. J. ORG. CHEMC
  148031. GARNER; AZIRIDINE, 2
  148032. ACYL, CHIRAL AUXILIARY, THERMAL RING OPENING, DIPOLAR CYCLOADDITION, PYRROLIDINE, ASYMMETRIC, GLYCINE IMINE, PROTOTROPIC SHIFTM
  148033. 6450N
  148034. 2/28/96VVAUXILIARY CONTROLLED 1,3
  148035. DIPOLAR CYCLOADDITIONS OF CHIRAL STABILIZED AZOMETHINE YLIDES
  148036. 1994 59 4
  148037. GABRIEL WEATHERHEAD
  148038. RES. CHEM. INTERMEDCmMAJETICH; MICROWAVE, REVIEW, DIELS
  148039. ALDER, CLAISEN REARRANGEMENT, ENE, SUBSTITUTION, OXIDATION, ESTERIFICATIONM
  148040. 6451N
  148041. 2/28/96V7APPLICATIONS OF MICROWAVE ACCELERATED ORGANIC CHEMISTRYW
  148042. 1994 20 61
  148043. GABRIEL WEATHERHEAD
  148044. 6452N
  148045. 2/28/96V
  148046. WALLING, CHEVES. FIFTY YEARS OF FREE RADICALS (PROFILES, PATHWAYS AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS, JEFFREY I. SEEMAN, ED.). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1994. A REVIEWa
  148047. GABRIEL WEATHERHEAD
  148048. 6453N
  148049. 2/28/96V
  148050. PATAI, SAUL; RAPPOPORT, ZVI, EDS. SUPPLEMENT S: THE CHEMISTRY OF SULFUR
  148051. CONTAINING FUNCTIONAL GROUPS (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U. K., 1993. A REVIEWa
  148052. GABRIEL WEATHERHEAD
  148053. 6454N
  148054. 2/28/96V9HUISGEN, ROLF. THE ADVENTURE PLAYGROUND ON THE . A REVIEWa
  148055. GABRIEL WEATHERHEAD
  148056. 6455N
  148057. 2/28/96
  148058. VaHASLAM, EDWIN. SHIKIMIC ACID. METABOLISM AND METABOLITES. WILEY: CHICHESTER, U.K., 1993. A REVIEWa
  148059. GABRIEL WEATHERHEAD
  148060. 6456N
  148061. 2/28/96V
  148062. CASY, ALAN F. THE STERIC FACTOR IN MEDICINAL CHEMISTRY. DISSYMMETRIC PROBES OF PHARMACOLOGICAL RECEPTORS. PLENUM: NEW YORK, 1993. A REVIEWa
  148063. GABRIEL WEATHERHEAD
  148064. 6457N
  148065. 2/28/96V
  148066. BLOMBERG, CORNELIS. THE BARBIER REACTION AND RELATED ONE
  148067. STEP PROCESSES (REACTIVITY AND STRUCTURE. CONCEPTS IN ORGANIC CHEMISTRY, VOL. 31). SPRINGERVERLAG: BERLIN, 1993. A REVIEWa
  148068. GABRIEL WEATHERHEAD
  148069. 6458N
  148070. 2/28/96VyBARTON, DEREK H. R. HALF A CENTURY OF FREE RADICAL CHEMISTRY. CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, U.K., 1993. A REVIEWa
  148071. GABRIEL WEATHERHEAD
  148072. 6459N
  148073. 2/28/96V
  148074. UEMURA, MOTOKAZU. CHIRAL (N6
  148075. ARENE)CHROMIUM COMPLEXES IN ORGANIC SYNTHESIS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148076. GABRIEL WEATHERHEAD
  148077. 6460N
  148078. 2/28/96
  148079. 7OKUBO, MASAO; MATSUO, KOJI. N
  148080. MG REAGENTS: VARIETY OF REACTION MODES FOR C
  148081. N AND N
  148082. N BOND FORMATION
  148083. REACTIVITY OF N
  148084. MG AND C
  148085. MG REAGENTS SYSTEMATIZED IN TERMS OF RELATIVE SINGLE
  148086. ELECTRON TRANSFER EFFICIENCY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994.  . A REVIEW
  148087. GABRIEL WEATHERHEAD
  148088. 6461N
  148089. 2/28/96V
  148090. TANAKA, KAZUHIKO. STEREOFACE DIFFERENTIATION IN ASYMMETRIC SYNTHESIS USING CHIRAL 3
  148091. AMINO
  148092. HYDROXYBORNANES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148093. GABRIEL WEATHERHEAD
  148094. 6462N
  148095. 2/28/96V
  148096. FUCHIGAMI, TOSHIO. SELECTIVE ANODIC PARTIAL FLUORINATION OF HETEROATOM COMPOUNDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148097. GABRIEL WEATHERHEAD
  148098. 6463N
  148099. 2/28/96
  148100. UMEMOTO, TERUO. RECENT DEVELOPMENT OF FLUORINATING AGENTS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148101. GABRIEL WEATHERHEAD
  148102. 6464N
  148103. 2/28/96V
  148104. TROEV, KOLJO. DIALKYL HYDROGEN PHOSPHONATES. 2. SUBSTITUTION REACTIONS AT PHOSPHORUS ATOM. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148105. GABRIEL WEATHERHEAD
  148106. 6465N
  148107. 2/28/96V
  148108. MEMMESHEIMER, HOLGER; REGITZ, MANFRED. 1
  148109. PHOSPHIRENES: SYNTHESIS AND PREPARATIVE SIGNIFICANCE IN ORGANOPHOSPHORUS CHEMISTRY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148110. GABRIEL WEATHERHEAD
  148111. 6466N
  148112. 2/28/96V
  148113. OGAWA, AKIYA; SONODA, NOBORU. SYNTHETIC UTILITY OF SELENIUM
  148114. CARBON MONOXIDE
  148115. WATER REACTION SYSTEM. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148116. GABRIEL WEATHERHEAD
  148117. 6467N
  148118. 2/28/96V
  148119. RYASHENTSEVA, MARAGARITA A. CATALYTIC SYNTHESIS OF THIOPHENE AND ALKYLTHIOPHENES VIA HETEROCYCLIZATION REACTION. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148120. GABRIEL WEATHERHEAD
  148121. 6468N
  148122. 2/28/96V
  148123. LOZAC'H, NOEL. FACTS AND WORDS IN HETEROATOMIC NOMENCLATURE. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 10. SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1994. A REVIEWa
  148124. GABRIEL WEATHERHEAD
  148125. 6469N
  148126. 2/28/96V
  148127. CHAKRABORTY, D. P. CHEMISTRY AND BIOLOGY OF CARBAZOLE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 44. GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORK, 1993. A REVIEWa
  148128. GABRIEL WEATHERHEAD
  148129. 6470N
  148130. 2/28/96V
  148131. TAKAHATA, HIROKI; MOMOSE, TAKEFUMI. SIMPLE INDOLIZIDINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 44. GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORK, 1993. A REVIEWa
  148132. GABRIEL WEATHERHEAD
  148133. 6471N
  148134. 2/28/96V
  148135. ROBINS, RICHARD J.; WALTON, NICHOLAS J. THE BIOSYNTHESIS OF TROPANE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 44. GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORK, 1993. A REVIEWa
  148136. GABRIEL WEATHERHEAD
  148137. 6472N
  148138. 2/28/96V
  148139. LAUNASMAA, MAURI; TAMMINEN, TARJA. THE TROPANE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 44. GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORK, 1993. A REVIEWa
  148140. GABRIEL WEATHERHEAD
  148141. 6473N
  148142. 2/28/96
  148143. GORDON, M. S.; FRANCISCO, J. S.; SCHLEGEL, H. B. THEORETICAL INVESTIGATIONS OF THE THERMOCHEMISTRY AND THERMAL DECOMPOSITION OF SILANES, HALOSILANES, AND ALKYLSILANES.  ADVANCES IN SILICON CHEMISTRY. VOLUME 2. GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEW
  148144. GABRIEL WEATHERHEAD
  148145. 6474N
  148146. 2/28/96
  148147. DAMRAUER, ROBERT. GAS PHASE STUDIES ON THE NEGATIVE ION CHEMISTRY OF SILICON.  ADVANCES IN SILICON CHEMISTRY. VOLUME 2. GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  148148. GABRIEL WEATHERHEAD
  148149. 6475N
  148150. 2/28/96V
  148151. HUDRLIK, PAUL F.; HUDRLIK, ANNE M. A,,B
  148152. EPOXYSILANES. ADVANCES IN SILICON CHEMISTRY. VOLUME 2. GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  148153. GABRIEL WEATHERHEAD
  148154. 6476N
  148155. 2/28/96V
  148156. MASUYAMA, YOSHIRO. PALLADIUM
  148157. CATALYZED CARBONYL ALLYLATION VIA PI
  148158. ALLYLPALLADIUM COMPLEXES. ADVANCES IN METAL
  148159. ORGANIC CHEMISTRY. VOLUME 3. LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148160. GABRIEL WEATHERHEAD
  148161. 6477N
  148162. 2/28/96V
  148163. MURAHASHI, SHUN
  148164.  NAOTA, TAKESHI. RUTHENIUM
  148165. CATALYZED OXIDATIVE TRANSFORMATIONS OF ALCOHOLS. ADVANCES IN METAL
  148166. ORGANIC CHEMISTRY. VOLUME 3. LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148167. GABRIEL WEATHERHEAD
  148168. 2/28/96V
  148169. LAROCK, RICHARD C. PALLADIUM
  148170. CATALYZED VINYLIC SUBSTITUTION. ADVANCES IN METAL
  148171. ORGANIC CHEMISTRY. VOLUME 3. LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148172. GABRIEL WEATHERHEAD
  148173. 6479N
  148174. 2/28/96
  148175. 9HERNDON, JAMES W.; TUMER, SENIZ U.; MCMULLEN, LEONARD A.; MATASI, JULIUS J.; SCHNATTER, WAYNE F. K. CYCLOPROPYLCARBENE
  148176. CHROMIUM COMPLEXES: VERSATILE REAGENTS FOR THE SYNTHESIS OF FIVE
  148177. MEMBERED RINGS. ADVANCES IN METAL
  148178. ORGANIC CHEMISTRY. VOLUME 3. LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEW
  148179. GABRIEL WEATHERHEAD
  148180. 6480N
  148181. 2/28/96V
  148182. MAIN, LYNDSAY; NICHOLSON, BRIAN K. ORTHOMAN GANATED ARYL KETONES AND RELATED COMPOUNDS IN ORGANIC SYNTHESIS .ADVANCES IN METAL
  148183. ORGANIC CHEMISTRY. VOLUME 3. LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148184. GABRIEL WEATHERHEAD
  148185. 6481N
  148186. 2/28/96
  148187. BAILEY, WILLIAM F.; OVASKA, TIMO V. GENERATION AND CYCLIZATION OF UNSATURATED ORGANOLITHIUMS.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148188. GABRIEL WEATHERHEAD
  148189. 6482N
  148190. 2/28/96V
  148191. BENJES, PAUL A.; GRIMMETT, M. ROSS. N
  148192. ALKYLATION OF NITROGEN AZOLES.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148193. GABRIEL WEATHERHEAD
  148194. 6483N
  148195. 2/28/96V
  148196. OTERA, JUNZO. TEMPLATE EFFECTS OF DISTANNOXANES.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148197. GABRIEL WEATHERHEAD
  148198. 6484N
  148199. 2/28/96V
  148200. COXON, JAMES A.; MCDONALD, D. QUENTIN; STEEL, PETER J. DIASTEREOFACIAL SELECTIVITY IN THE DIELS
  148201. ALDER REACTION.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148202. GABRIEL WEATHERHEAD
  148203. 6485N
  148204. 2/28/96V
  148205. SMITH, ROBIN A. J.; VELLEKOOP, A. SAMUEL. 1,4 ADDITION REACTIONS OF ORGANOCUPRATES WITH A,B
  148206. UNSATURATED KETONES.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148207. GABRIEL WEATHERHEAD
  148208. 6486N
  148209. 2/28/96V
  148210. MIKAMI, KOICHI; SHIMIZU, MASAKI. STEREOELECTRONIC RULES IN ADDITION REACTIONS: "CRAM'S RULE" IN OLEFINIC SYSTEMS.  ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148211. GABRIEL WEATHERHEAD
  148212. 6487N
  148213. 2/28/96V
  148214. YAMAMOTO, YOSHINORI; SHIDA, NAOMI. STEREOCHEMISTRY AND MECHANISM OF ALLYLIC TIN
  148215. ALDEHYDE CONDENSATION REACTIONS. ADVANCES IN DETAILED REACTION MECHANISMS. VOLUME 3. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148216. GABRIEL WEATHERHEAD
  148217. 6488N
  148218. 2/28/96
  148219. MEMMESHEIMER, HOLGER; REGITZ, MANFRED. THE ROLE OF CARBENES IN THE CHEMISTRY OF LOW
  148220. COORDINATED PHOSPHORUS. ADVANCES IN CARBENE CHEMISTRY. VOLUME 1. UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148221. GABRIEL WEATHERHEAD
  148222. 6489N
  148223. 2/28/96V
  148224. JONES, MAITLAND, JR. CARBENES AND CARBORANES. ADVANCES IN CARBENE CHEMISTRY. VOLUME 1. UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148225. GABRIEL WEATHERHEAD
  148226. 6490N
  148227. 2/28/96V
  148228. JACKSON, JAMES E.; PLATZ, MATTHEW S. LASER FLASHPHOTOLYSIS STUDIES OF YLIDE
  148229. FORMING REACTIONS OF CARBENES. ADVANCES IN CARBENE CHEMISTRY. VOLUME 1. UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148230. GABRIEL WEATHERHEAD
  148231. 6491N
  148232. 2/28/96V
  148233. MOSS, ROBERT A. ABSOLUTE KINETICS OF INTRAMOLECULAR ALKLYCARBENE REACTIONS.  ADVANCES IN CARBENE CHEMISTRY. VOLUME 1. UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148234. GABRIEL WEATHERHEAD
  148235. 6492N
  148236. 2/28/96
  148237. KIRMSE, WOLFGANG. CARBENES AND THE O
  148238. H BOND. ADVANCES IN CARBENE CHEMISTRY. VOLUME 1. UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CT, 1994. A REVIEWa
  148239. GABRIEL WEATHERHEAD
  148240. 6493N
  148241. 2/28/96V
  148242. BURES, MARK G.; MARTIN, YVONNE C.; WILLETT, PETER. SEARCHING TECHNIQUES FOR DATABASES OF THREEDIMENSIONAL CHEMICAL STRUCTURES. TOPICS IN STEREOCHEMISTRY, 1994, 21, 467
  148243. 511. A REVIEWa
  148244. GABRIEL WEATHERHEAD
  148245. 6494N
  148246. 2/28/96V
  148247. YOUNG, DOUGLAS W. STEREOCHEMISTRY OF METABOLIC REACTIONS OF AMINO ACIDS. TOPICS IN STEREOCHEMISTRY, 1994, 21, 381
  148248. 465. A REVIEWa
  148249. GABRIEL WEATHERHEAD
  148250. 6495N
  148251. 2/28/96V
  148252. DODZIUK, HELENA. UNUSUAL SATURATED HYDROCARBONS: INTERACTION BETWEEN THEORETICAL AND SYNTHETIC CHEMISTRY. TOPICS IN STEREOCHEMISTRY, 1994, 21, 351
  148253. 380. A REVIEWa
  148254. GABRIEL WEATHERHEAD
  148255. 6496N
  148256. 2/28/96
  148257. GRACZYK, PIOTR P.; MIKOLAJCZYK, MARIAN. ANOMERIC EFFECT: ORIGIN AND CONSEQUENCES. TOPICS IN STEREOCHEMISTRY, 1994, 21, 159
  148258. 349. A REVIEWa
  148259. GABRIEL WEATHERHEAD
  148260. 6497N
  148261. 2/28/96V
  148262. VEDEJS, E.; PETERSON, M. J. STEREOCHEMISTRY AND MECHANISM IN THE WITTIG REACTION. TOPICS IN STEREOCHEMISTRY, 1994, 21,1
  148263. 157. A REVIEWa
  148264. GABRIEL WEATHERHEAD
  148265. 6498N
  148266. 2/28/96V
  148267. FOOTE, CHRISTOPHER S. PHOTOPHYSICAL AND PHOTOCHEMICAL PROPERTIES OF FULLERENES. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 347. A REVIEWa
  148268. GABRIEL WEATHERHEAD
  148269. 6499N
  148270. 2/28/96V
  148271. MIZUNO,KAZUHIKO;OTSUJI,YOSHIO. ADDITION AND CYCLOADDITION REACTIONS VIA PHOTOINDUCED ELECTRON TRANSFER. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 301. A REVIEWa
  148272. GABRIEL WEATHERHEAD
  148273. 6500N
  148274. 2/28/96
  148275. RETTIG, WOLFGANG. PHOTOINDUCED CHARGE SEPARATION VIA TWISTED INTRAMOLECULAR CHARGE TRANSFER STATES. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 253. A REVIEWa
  148276. GABRIEL WEATHERHEAD
  148277. 6501N
  148278. 2/28/96V
  148279. KAIM, WOLFGANG. THERMAL AND LIGHT INDUCED ELECTRON TRANSFER REACTIONS OF MAIN GROUP METAL HYDRIDES AND ORGANOMETALLICS. TOPICS IN CURRENT CHEMISTRY, 1994, 169 (ELECTRON TRANSFER I), 231. A REVIEWa
  148280. GABRIEL WEATHERHEAD
  148281. 6502N
  148282. 2/28/96V
  148283. SCHMITTEL, MICHAEL. UMPOLUNG OF KETONES VIA ENOL RADICAL CATIONS. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 183. A REVIEWa
  148284. GABRIEL WEATHERHEAD
  148285. 6503N
  148286. 2/28/96V
  148287. MEMMING, RUDIGER. PHOTOINDUCED CHARGE TRANSFER PROCESSES AT SEMICONDUCTOR ELECTRODES AND PARTICLES. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 105. A REVIEWa
  148288. GABRIEL WEATHERHEAD
  148289. 6504N
  148290. 2/28/96
  148291. BAUMGARTEN, MARTIN; MULLEN, KLAUS. RADICAL IONS: WHERE ORGANIC CHEMISTRY MEETS MATERIALS SCIENCES. TOPICS IN CURRENT CHEMISTRY, 1994,169 (ELECTRON TRANSFER I), 1. A REVIEWa
  148292. GABRIEL WEATHERHEAD
  148293. 6505N
  148294. 2/28/96
  148295. 2BISSELL, RICHARD A.; DESILVA, A. PRASANNA; GUNARATNE, H. Q. NIMAL; LYNCH, P. L. MARK; MAGUIRE, GLENN E. M.; MCCOY, COLIN P.; SANDANAYAKE, K. R. A. SAMANKUMARA. FLUORESCENT PET (PHOTOINDUCED ELECTRON TRANSFER) SENSORS. TOPICS IN CURRENT CHEMISTRY, 1993, 168 (PHOTOINDUCED ELECTRON TRANSFER V), 223. A REVIEW
  148296. GABRIEL WEATHERHEAD
  148297. 6506N
  148298. 2/28/96V
  148299. PANDEY, GANESH. PHOTOINDUCED ELECTRON TRANSFER (PET) IN ORGANIC SYNTHESIS. TOPICS IN CURRENT CHEMISTRY, 1993, 168 (PHOTOINDUCED ELECTRON TRANSFER V), 175. A REVIEWa
  148300. GABRIEL WEATHERHEAD
  148301. 6507N
  148302. 2/28/96
  148303. ALBINI, ANGE LO; FASANI, ELISA; MELLA, MARIELLA. PET
  148304. REACTIONS OF AROMATIC COMPOUNDS. TOPICS IN CURRENT CHEMISTRY, 1993,168 (PHOTO INDUCED ELECTRON TRANSFER V), 143. A REVIEWa
  148305. GABRIEL WEATHERHEAD
  148306. 6508N
  148307. 2/28/96V
  148308. SOUMILLION, JEAN
  148309. PHILIPPE. PHOTOINDUCED ELECTRON TRANSFER EMPLOYING ORGANIC ANIONS. TOPICS IN CURRENT CHEMISTRY, 1993,168 (PHOTO INDUCED ELECTRON TRANSFER V), 93. A REVIEWa
  148310. GABRIEL WEATHERHEAD
  148311. 6509N
  148312. 2/28/96V
  148313. FREEMAN, PETER K.; HATLEVIG, SUSAN A. THE PHOTOCHEMISTRY OF POLYHALOCOMPOUNDS, DEHALOGENATION BY PHOTO INDUCED ELECTRON TRANSFER, NEW METHODS OF TOXIC WASTE DISPOSAL. TOPICS IN CURRENT CHEMISTRY, 1993,168 (PHOTOINDUCED ELECTRON TRANSFER V), 47. A REVIEWa
  148314. GABRIEL WEATHERHEAD
  148315. 6510N
  148316. 2/28/96V
  148317. MASLAK, PRZEMYSLAW . FRAGMENTATIONS BY PHOTOINDUCED ELECTRON TRANSFER. FUNDAMENTALS AND PRACTICAL .SPECTS. TOPICS IN CURRENT CHEMISTRY, 1993,168 (PHOTOINDUCED ELECTRON TRANSFER V), 1. A REVIEWa
  148318. GABRIEL WEATHERHEAD
  148319. 6511N
  148320. 2/28/96VyGANT, THOMAS G.; MEYERS, A. I. THE CHEMISTRY OF 2
  148321. OXAZOLINES (1985
  148322. PRESENT). TETRAHEDRON, 1994, 50(8), 2297
  148323. 360. A REVIEWa
  148324. GABRIEL WEATHERHEAD
  148325. 6512N
  148326. 2/28/96V
  148327. DUTHALER, RUDOLF O. RECENT DEVELOPMENTS IN THE STEREOSELECTIVE SYNTHESIS OF A
  148328. AMINO ACIDS. TETRAHEDRON, 1994, 50(6), 1539
  148329. 660. A REVIEWa
  148330. GABRIEL WEATHERHEAD
  148331. 6513N
  148332. 2/28/96V
  148333. MAGNUS, PHILIP. A GENERAL STRATEGY USING N2 CO2(CO)6 ACETYLENE COMPLEXES FOR THE SYNTHESIS OF THE ENEDIYNE ANTITUMOR AGENTS ESPERAMICIN, CALICHEAMICIN, DYNEMICIN AND NEOCARZINOSTATIN. TETRAHEDRON, 1994, 50(5),1397
  148334. 418. A REVIEWa
  148335. GABRIEL WEATHERHEAD
  148336. 6514N
  148337. 2/28/96V
  148338. ALBINI, ANGELO; MELLA, MARIELLA; FRECCERO, MAURO. A NEW METHOD IN RADICAL CHEMISTRY: GENERATION OF RADICALS BY PHOTO
  148339. INDUCED ELECTRON TRANSFER AND FRAGMENTATION OF THE RADICAL CATION. TETRAHEDRON, 1994, 50(3), 575
  148340. 607. A REVIEWa
  148341. GABRIEL WEATHERHEAD
  148342. 6515N
  148343. 2/28/96
  148344. DIAS, JERRY RAY. DECIPHERING THE INFORMATION CONTENT OF POLYCYCLIC CONJUGATED HYDROCARBON FORMULAS
  148345. FROM BENZENOIDS TO FULLERENES. TETRAHEDRON, 1993, 49(41), 9207
  148346. 20. A REVIEWa
  148347. GABRIEL WEATHERHEAD
  148348. 6516N
  148349. 2/28/96V
  148350. OSTERHOUT, MARTIN H.; NADLER, WILLIAM R.; PADWA, ALBERT. RECENT ADVANCES IN THE CYCLOADDITION CHEMISTRY OF ISOMUNCHNONES AND THIOISOMUNCHNONES, AN UNDERUTILIZED CLASS OF MESOIONIC COMPOUNDS.  SYNTHESIS, 1994, (2),123
  148351. 141. A REVIEWa
  148352. GABRIEL WEATHERHEAD
  148353. 6517N
  148354. 2/28/96VhJARAMILLO, CARLOS; KNAPP, SPENCER. SYNTHESIS OF C
  148355. ARYL GLYCOSIDES.  SYNTHESIS, 1994, (1), 1
  148356. 20. A REVIEWa
  148357. GABRIEL WEATHERHEAD
  148358. 6518N
  148359. 2/28/96VwRODRIGUEZ, JEAN; DULCERE, JEAN PIERRE. COHALOGENATION IN ORGANIC SYNTHESIS.  SYNTHESIS, 1993, (12), 1177
  148360. 1205. A REVIEWa
  148361. GABRIEL WEATHERHEAD
  148362. 6519N
  148363. 2/28/96
  148364. BANFI, LUCA; GUANTI, GIUSEPPE. ASYMMETRIZED 2
  148365. METHYL
  148366. PROPANEDIOL AND ITS EQUIVALENTS: PREPARATION AND SYNTHETIC APPLICATIONS.  SYNTHESIS, 1993, (11), 1029
  148367. 56. A REVIEWa
  148368. GABRIEL WEATHERHEAD
  148369. 6520N
  148370. 2/28/96V
  148371. KEGLEVICH, GYORGY. SYNTHESIS OF 6
  148372.  AND 7
  148373. MEMBERED PHOSPHORUS HETEROCYCLES BY RING ENLARGEMENT. SYNTHESIS, 1993, (10), 931
  148374. 42. A REVIEWa
  148375. GABRIEL WEATHERHEAD
  148376. 6521N
  148377. 2/28/96V
  148378. ELNAGDI, MOHAMED HILMY; NEGM, ABDALLA MOHAMED; SADEK, KAMAL USEF. ALKYLHETEROAROMATICS AS BUILDING BLOCKS FOR THE SYNTHESIS OF CONDENSED POLYFUNCTIONALLY SUBSTITUTED HETEROCYCLES. SYNLETT, 1994, (1), 27
  148379. 37. A REVIEWa
  148380. GABRIEL WEATHERHEAD
  148381. 6522N
  148382. 2/28/96V
  148383. SMADJA, WILLIAM. ACYCLIC DIASTEREOFACIAL SELECTION IN INTERMOLECULAR RADICAL REACTIONS. STERIC VS. ELECTRONIC CONTROLS. SYNLETT, 1994, (1), 1
  148384. 26. A REVIEWa
  148385. GABRIEL WEATHERHEAD
  148386. 6523N
  148387. 2/28/96
  148388. VoRANU, BRINDABAN C. ZINC BOROHYDRIDE
  148389. A REDUCING AGENT WITH HIGH POTENTIAL. SYNLETT, 1993, (12), 885
  148390. 92. A REVIEWa
  148391. GABRIEL WEATHERHEAD
  148392. 6524N
  148393. 2/28/96
  148394. (SONAWANE, HARIKISAN R.; BELLUR, NANJUNDIAH S.; KULKARNI, DILIP G.; AHUJA, JAIMALA R. PHOTOINDUCED VINYLCYCLOPROPANE
  148395. CYCLOPENTENE REARRANGEMENT (PHOTO
  148396. CP): A METHODOLOGY FOR CHIRAL BICYCLO[3.2.0]HEPTENES AND THEIR APPLICATION IN NATURAL PRODUCT SYNTHESES. SYNLETT, 1993, (12), 875
  148397. 84. A REVIEW
  148398. GABRIEL WEATHERHEAD
  148399. 6525N
  148400. 2/28/96V
  148401. KAHN, MICHAEL. PEPTIDE SECONDARY STRUCTURE MIMETICS: RECENT ADVANCES AND FUTURE CHALLENGES. SYNLETT, 1993, (11), 821
  148402. 6. A REVIEWa
  148403. GABRIEL WEATHERHEAD
  148404. 6526N
  148405. 2/28/96VaNORTH, MICHAEL. CATALYTIC ASYMMETRIC CYANOHYDRIN SYNTHESIS. SYNLETT, 1993, (11), 807
  148406. 20. A REVIEWa
  148407. GABRIEL WEATHERHEAD
  148408. 6527N
  148409. 2/28/96
  148410. ASFARI, ZOUHAIR; WEISS, JEAN; VICENS, JACQUES. DOUBLE
  148411. CALIXARENE DESIGN, SYNTHESIS, AND PROPERTIES. SYNLETT, 1993, (10), 719
  148412. 25. A REVIEWa
  148413. GABRIEL WEATHERHEAD
  148414. 6528N
  148415. 2/28/96V
  148416. ZEFIROV, NIKOLAI S.; ZYK, NIKOLAI V.; BELOGLAZKINA, ELENA K.; KUTATELADZE, ANDREI G. THIOSULFONATES: SYNTHESIS, REACTIONS AND PRACTICAL APPLICATIONS. SULFUR REPORTS, 1993, 14, 223
  148417. 40. A REVIEWa
  148418. GABRIEL WEATHERHEAD
  148419. 6529N
  148420. 2/28/96VwKOVAL, IVAN V. ADVANCES IN THE CHEMISTRY OF SULFIMIDES AND RELATED COMPOUNDS. SULFUR REPORTS, 1993,14,149
  148421. 215. A REVIEWa
  148422. GABRIEL WEATHERHEAD
  148423. 6530N
  148424. 2/28/96VyTAKAHASHI, MASAKI; OKAZAKI, RENJI. THE CHEMISTRY OF THIONITROSO COMPOUNDS. SULFUR REPORTS, 1993, 13(2), 293
  148425. 341. A REVIEWa
  148426. GABRIEL WEATHERHEAD
  148427. 6531N
  148428. 2/28/96V
  148429. MITCHELL, S. C.; NICKSON, R. M.; WARING, R. H. THE BIOLOGICAL ACTIVITY OF SELENIUM SULFIDE. SULFUR REPORTS, 1993,13(2), 279
  148430.  92. A REVIEWa
  148431. GABRIEL WEATHERHEAD
  148432. 6532N
  148433. 2/28/96VrFIELD, LAMAR. FORTY
  148434. FIVE YEARS WITH A HYDRA, ORGANOSULFUR CHEMISTRY. SULFUR REPORTS, 1993,13(2), 197
  148435. 277. A REVIEWa
  148436. GABRIEL WEATHERHEAD
  148437. 6533N
  148438. 2/28/96VyMITCHELL, S. C.; NICKSON, R. M. METABOLISM OF SULFUR
  148439. CONTAINING XENOBIOTICS. SULFUR REPORTS, 1993,13(2), 161
  148440. 95. A REVIEWa
  148441. GABRIEL WEATHERHEAD
  148442. 6534N
  148443. 2/28/96V
  148444. DERYAGINA, E. N.; VORONKOV, M. G.; KORCHEVIN, N. A. SELENIUM
  148445.  AND TELLURIUM
  148446. CENTRED RADICALS. RUSSIAN CHEMICAL REVIEWS, 1993, 62(12), 1107. A REVIEWa
  148447. GABRIEL WEATHERHEAD
  148448. 6535N
  148449. 2/28/96V
  148450. ESIPENKO, A. A.; SAMARAI, L. I. CYCLOADDITION OF NITRILE OXIDES TO MULTIPLE BONDS CONTAINING A HETEROATOM. RUSSIAN CHEMICAL REVIEWS, 1993, 62(12), 1097. A REVIEWa
  148451. GABRIEL WEATHERHEAD
  148452. 6536N
  148453. 2/28/96V;USOV, A. I. OLIGOSACCHARINS
  148454. A NEW CLASS OF SIGNAL. A REVIEWa
  148455. GABRIEL WEATHERHEAD
  148456. 6537N
  148457. 2/28/96
  148458. VcGINZBURG, A. G. THE CHEMISTRY OF CYMANTRENE. RUSSIAN CHEMICAL REVIEWS, 1993, 62(11), 1025. A REVIEWa
  148459. GABRIEL WEATHERHEAD
  148460. 6538N
  148461. 2/28/96V
  148462. SOKOLYUK, N. T.; ROMANOV, V. V.; PISULINA, L. P. NAPHTHACENEQUINONES: SYNTHESIS AND PROPERTIES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(11), 1005. A REVIEWa
  148463. GABRIEL WEATHERHEAD
  148464. 6539N
  148465. 2/28/96V
  148466. KARTASHOV, V. R.; SKOROBOGATOVA, E. V.; ZEFIROV, N. S. REACTIONS OF CYCLOPROPENE DERIVATIVES WITH ELECTROPHILES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(10), 935. A REVIEWa
  148467. GABRIEL WEATHERHEAD
  148468. 6540N
  148469. 2/28/96V
  148470. BRODSKAYA, E. I.; RATOVSKII, G. V.; VORONKOV, M. G. ORBITAL INTERACTION THROUGH SPACE AND THROUGH O
  148471. BONDS. RUSSIAN CHEMICAL REVIEWS, 1993, 62(10), 919. A REVIEWa
  148472. GABRIEL WEATHERHEAD
  148473. 6541N
  148474. 2/28/96VfAVOTINS, F. AMINOACIDS OF THE CYCLOBUTANE SERIES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(9), 897. A REVIEWa
  148475. GABRIEL WEATHERHEAD
  148476. 6542N
  148477. 2/28/96
  148478. KDORFMAN, YA. A.; ALESHKOVA, M. M.; POLIMBETOVA, G. S.; LEVINA, L. V.; PETROVA, T. V.; ABDREIMOVA, R. R.; DOROSHKEVICH, D. M. NEW REACTIONS INVOLVING THE OXIDATIVE O
  148479. , AND C
  148480. PHOSPHORYLATION OF ORGANIC COMPOUNDS BY PHOSPHORUS AND PHOSPHIDES IN THE PRESENCE OF METAL COMPLEXES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(9), 877. A REVIEW
  148481. GABRIEL WEATHERHEAD
  148482. 6543N
  148483. 2/28/96V
  148484. KULINKOVICH, O. G. ACTIVATED CYCLOPROPANES IN THE SYNTHESIS OF FIVE
  148485. MEMBERED CARBOCYCLES AND HETEROCYCLES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(9), 839. A REVIEWa
  148486. GABRIEL WEATHERHEAD
  148487. 6544N
  148488. 2/28/96V
  148489. TOMILOV, YU. V.; DOKICHEV, V. A.; DZHEMILEV, U. M.; NEFEDOV, O. M. CATALYTIC DECOMPOSITION OF DIAZOMETHANE AS A GENERAL METHOD FOR THE METHYLENATION OF CHEMICAL COMPOUNDS. RUSSIAN CHEMICAL REVIEWS, 1993, 62(9), 803. A REVIEWa
  148490. GABRIEL WEATHERHEAD
  148491. 6545N
  148492. 2/28/96
  148493. V[VOLKOV, S. K. IMMUNOASSAY OF ALKALOIDS. RUSSIAN CHEMICAL REVIEWS, 1993,62(8), 787. A REVIEWa
  148494. GABRIEL WEATHERHEAD
  148495. 6546N
  148496. 2/28/96VVKOVAL', I. V. THIOLS AS SYNTHONS. RUSSIAN CHEMICAL REVIEWS, 1993, 62(8), 769. A REVIEWa
  148497. GABRIEL WEATHERHEAD
  148498. 6547N
  148499. 2/28/96V
  148500. KEIKO, N. A., VORONKOV, M. G. METHODS OF SYNTHESIS OF ACROLEIN AND ITS A
  148501. SUBSTITUTED DERIVATIVES. RUSSIAN CHEMICAL REVIEWS, 1993, 62(8), 751. A REVIEWa
  148502. GABRIEL WEATHERHEAD
  148503. 6548N
  148504. 2/28/96V
  148505. AMABILINO, DAVID B.; STODDART, J. FRASER. SELF ASSEMBLY AND MACROMOLECULAR DESIGN. PURE AND APPLIED CHEMISTRY, 1993, 65(11), 2351
  148506. 9. A REVIEWa
  148507. GABRIEL WEATHERHEAD
  148508. 6549N
  148509. 2/28/96V
  148510. BRODESSER, G.; CUETHER, R.; HOSS, R.; MEIER, S.; OTTENS, HILDEBRANDT S.; SCHMITZ, J.; VOEGTLE, F. NEW TAILORED HOSTS: FROM MOLECULAR RECOGNITION TO MECHANICAL BONDS. PURE AND APPLIED CHEMISTRY, 1993, 65(11), 2325
  148511. 8. A REVIEWa
  148512. GABRIEL WEATHERHEAD
  148513. 2/28/96
  148514. MURAKAMI, YUKITO; HAYASHIDA, OSAMU; ONO, KA ZUYA; HISAEDA, YOSHIO. THERMODYNAMICAL AND GEOMETRICAL CHARACTERIZATION OF MOLECULAR RECOGNITION BY CAGE
  148515. TYPE AND PEPTIDE AZAPARACYCLOPHANES IN AQUEOUS MEDIA. PURE AND APPLIED CHEMISTRY, 1993, 65(11), 2319
  148516. 24. A REVIEW
  148517. GABRIEL WEATHERHEAD
  148518. 6551N
  148519. 2/28/96V
  148520. ANDREU, CECILIA; BEERLI, RENE; BRANDA, NEIL; CONN, MORGAN; DE, MENDOZA JAVIER; GALAN, AMALIA; HUC, IVAN; ET AL. REPLICATION AND ASSEMBLY. PURE AND APPLIED CHEMISTRY, 1993, 65(11), 2313
  148521.  18. A REVIEWa
  148522. GABRIEL WEATHERHEAD
  148523. 6552N
  148524. 2/28/96V
  148525. BELOV, YURI P. CHIRAL MOBILE PHASES IN THE ENANTIOMERIC ANALYSIS AND IN THE EVALUATION OF STABILITY CONSTANTS OF PI
  148526. PI COMPLEXES. PURE AND APPLIED CHEMISTRY, 1993, 65(10), 2273
  148527. 80. A REVIEWa
  148528. GABRIEL WEATHERHEAD
  148529. 6553N
  148530. 2/28/96
  148531. ENGEWALD, W.; REINHARDT, R.; STEINBORN, A. THE USE OF SHAPE
  148532. SELECTIVE STATIONARY PHASES IN GC. PART 1: CYCLODEXTRIN PHASES. PURE AND APPLIED CHEMISTRY, 1993, 65(10), 2253
  148533. 6. A REVIEWa
  148534. GABRIEL WEATHERHEAD
  148535. 6554N
  148536. 2/28/96
  148537. LETARD, J. F.; LAPOUYADE, R.; RETTIG, W. SYNTHESIS AND PHOTOPHYSICAL STUDY OF 4
  148538. MONOAZA
  148539. CROWN
  148540. 5)STILBENES FORMING TWISTED INTRAMOLECULAR CHARGE TRANSFER STATES AND THEIR COMPLEXATION WITH CATIONS. PURE AND APPLIED CHEMISTRY, 1993, 65(8), 1705
  148541. 12. A REVIEW
  148542. GABRIEL WEATHERHEAD
  148543. 6555N
  148544. 2/28/96V
  148545. SZAJDZINSKA, PIETEK E.; GEBICKI, J. L.; KROH, J. SCAVENGING OF HYDRATED ELECTRONS BY HYDROPHOBIC SOLUTES IN IONIC MICELLAR SOLUTIONS. PURE AND APPLIED CHEMISTRY, 1993, 65(8), 1617
  148546. 23. A REVIEWa
  148547. GABRIEL WEATHERHEAD
  148548. 6556N
  148549. 2/28/96
  148550. ZHU, QI CONG; HUTCHINS, ROBERT O.; HUTCHINS, MARYGAIL K. ASYMMETRIC REDUCTIONS OF CARBON
  148551. NITROGEN DOUBLE BONDS. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994, 26(2), 193
  148552. 236. A REVIEWa
  148553. GABRIEL WEATHERHEAD
  148554. 6557N
  148555. 2/28/96V
  148556. KOTALI, ANTIGONI; HARRIS, PHILIP A. O
  148557. HYDROXYARYL KETONES IN ORGANIC SYNTHESIS.  ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994, 26(2), 159
  148558. 92. A REVIEWa
  148559. GABRIEL WEATHERHEAD
  148560. 6558N
  148561. 2/28/96V
  148562. OH, TAEBOEM; REILLY, MICHAEL. REAGENT
  148563. CONTROLLED ASYMMETRIC DIELS
  148564. ALDER REACTIONS. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994. 26(2). 129
  148565. 58. A REVIEWa
  148566. GABRIEL WEATHERHEAD
  148567. 6559N
  148568. 2/28/96VbSHIBATA, IKUYA; BABA, AKIO. ORGANOTIN ENOLATES IN ORGANIC SYNTHESIS. 1994, 26(1), 85
  148569. 100. A REVIEWa
  148570. GABRIEL WEATHERHEAD
  148571. 6560N
  148572. 2/28/96
  148573. ALLEN, ANGELA J.; VAILLANCOURT, VALERIE; ALBIZATI, KIM F. FURANOSESQUITERPENE SYNTHESIS. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1994, 26(1), 1
  148574. 84. A REVIEWa
  148575. GABRIEL WEATHERHEAD
  148576. 6561N
  148577. 2/28/96V
  148578. HUGHES, DAVID L. PROGRESS IN THE FISCHER INDOLE REACTION. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1993, 25(6), 607
  148579. 32. A REVIEWa
  148580. GABRIEL WEATHERHEAD
  148581. 6562N
  148582. 2/28/96V
  148583. NATALE, NICHOLAS R.; MIRZAEI, YOUSEF R. THE LATERAL METALATION OF ISOXAZOLES. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1993, 25(5), 515
  148584. 56. A REVIEWa
  148585. GABRIEL WEATHERHEAD
  148586. 6563N
  148587. 2/28/96V
  148588. KARP, GARY M. PREPARATION AND REACTIONS OF INDOLIN
  148589. 2(3H)
  148590. ONES. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1993, 25(5), 481
  148591. 513. A REVIEWa
  148592. GABRIEL WEATHERHEAD
  148593. 6564N
  148594. 2/28/96
  148595. CLAUSEN, FINN PRIESS; JUHL, CHRISTENSEN JOERGEN. SYNTHESIS OF 9
  148596. SUBSTITUTED GUANINES. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL, 1993, 25(4), 375
  148597. 401. A REVIEWa
  148598. GABRIEL WEATHERHEAD
  148599. 6565N
  148600. 2/28/96VyO'HAGAN, D. BIOSYNTHESIS OF FATTY ACID AND POLYKETIDE METABOLITES. NATURAL PRODUCT REPORTS, 1993,10(6), 593
  148601. 624. A REVIEWa
  148602. GABRIEL WEATHERHEAD
  148603. 6566N
  148604. 2/28/96V
  148605. HERBERT, R. B. THE BIOSYNTHESIS OF PLANT ALKALOIDS AND NITROGENOUS MICROBIAL METABOLITES. NATURAL PRODUCT REPORTS, 1993, 10(6), 575
  148606. 92. A REVIEWa
  148607. GABRIEL WEATHERHEAD
  148608. 6567N
  148609. 2/28/96V
  148610. MURPHY, J. A.; GRIF3LTHS, J. A SURVEY OF NATURAL PRODUCTS WHICH ABSTRACT HYDROGEN ATOMS FROM NUCLEIC ACIDS. NATURAL PRODUCT REPORTS, 1993,10(6), 551
  148611. 64. A REVIEWa
  148612. GABRIEL WEATHERHEAD
  148613. 6568N
  148614. 2/28/96VgENDO, A.; HASUMI, K HMG
  148615. COA REDUCTASE INHIBITORS. NATURAL PRODUCT REPORTS, 1993,10(6), 541
  148616. 50. A REVIEWa
  148617. GABRIEL WEATHERHEAD
  148618. 2/28/96V
  148619. MODERHACK, DIETRICH. OXO
  148620.  AND IMINO
  148621. FUNCTIONALIZED 1,2
  148622. OXAZETIDINES. AN OVERVIEW. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30(3), 579. A REVIEWa
  148623. GABRIEL WEATHERHEAD
  148624. 6570N
  148625. 2/28/96V
  148626. CATSOULACOS, P.; CATSOULACOS, D. FORMATION OF HOMO
  148627. STEROIDS AND DERIVATIVES BY BECKMANN REARRANGEMENT. ANTITUMOR ACTIVITY OF STEREOISOMERS HOMOAZA
  148628. STEROIDAL ESTERS. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30(1),1
  148629. 10. A REVIEWa
  148630. GABRIEL WEATHERHEAD
  148631. 6571N
  148632. 2/28/96V
  148633. DEGA, SZAFRAN ZOFIA; SZAFRAN, MIROSLAW. COMPLEXES OF CARBOXYLIC ACIDS WITH PYRIDINES AND PYRIDINE N
  148634. OXIDES. HETEROCYCLES, 1994, 37(1), 627
  148635. 59. A REVIEWa
  148636. GABRIEL WEATHERHEAD
  148637. 6572N
  148638. 2/28/96V}PIOZZI, FRANCO. F'URTHER RESEARCHES ON THE FUROCLE RODANES FROM TEUCRIUM SPECIES. HETEROCYCLES, 1994, 37(1), 603
  148639. 26. A REVIEWa
  148640. GABRIEL WEATHERHEAD
  148641. 6573N
  148642. 2/28/96
  148643. MORENO, MANAS MARCIAL; PLEIXATS, ROSER. BICYCLIC COMPOUNDS STRUCTURALLY RELATED TO DEHYDROACETIC ACID AND TRIACETIC ACID LACTONE. HETEROCYCLES, 1994, 37(1), 585
  148644. 601. A REVIEWa
  148645. GABRIEL WEATHERHEAD
  148646. 6574N
  148647. 2/28/96V
  148648. BUTLER, RICHARD N.; OSHEA, DONAL F. SUBSTITUTED1,2,3
  148649. TRIAZOLIUM
  148650. YLIDES AS 1,3
  148651. DIPOLES: SYNTHONS FOR A RANGE OF AZIMINE AND 1,2,3
  148652. TRIAZA SYSTEMS. HETEROCYCLES, 1994, 37(1), 571
  148653. 84. A REVIEWa
  148654. GABRIEL WEATHERHEAD
  148655. 6575N
  148656. 2/28/96V
  148657. PELTER, ANDREW; WARD, ROBERT S. REACTIONS OF 2,6-DIARYL
  148658. DIOXABICYCLO[3.3.0]OCTANE LIGNANS. HETEROCYCLES, 1994, 37(1), 137
  148659. 47. A REVIEWa
  148660. GABRIEL WEATHERHEAD
  148661. 6576N
  148662. 2/28/96V
  148663. KATRITZKY, ALAN R. SUMMARY OF KATRITZKY RESEARCH GROUP SCIENTIFIC RESULTS (1954
  148664. 1993). HETEROCYCLES, 1994, 37(1), 3
  148665. 130. A REVIEWa
  148666. GABRIEL WEATHERHEAD
  148667. 6577N
  148668. 2/28/96
  148669. PRICE, WILLIAM A.; SILVA, ARTUR M. S.; CAVALEIRO,JOSE A. S. 2
  148670. STYRYLCHROMONES: BIOLOGICAL ACTION, SYNTHESIS AND REACTIVITY. HETEROCYCLES, 1993, 36(11), 2601
  148671. 11. A REVIEWa
  148672. GABRIEL WEATHERHEAD
  148673. 6578N
  148674. 2/28/96V
  148675. SLIWA, WANDA; CHRZASTEK, LIDIA; MIELNICZAK, MARIAN. HOST
  148676. GUEST COMPLEXES OF AZAAROMATIC QUATERNARY SALTS. HETEROCYCLES, 1993, 36(7),1645
  148677. 78. A REVIEWa
  148678. GABRIEL WEATHERHEAD
  148679. 6579N
  148680. 2/28/96VoHADDADIN. MAKHLUF J.; ISSIDORIDES, COSTAS H. THE BEIRUT REACTION.  HETEROCYCLES, 1993, 35(2), 1503
  148681. 25. A REVIEWa
  148682. GABRIEL WEATHERHEAD
  148683. 6580N
  148684. 2/28/96VgHASSNER, ALFRED; FISCHER, BILHA. NEW CHEMISTRYOF OXAZOLES. HETEROCYCLES, 1993, 35(2), 1441
  148685. 65. A REVIEWa
  148686. GABRIEL WEATHERHEAD
  148687. 6581N
  148688. 2/28/96V
  148689. MURRAY, WILLIAM V. ANGIOTENSIN II RECEPTORANTAGONISTS: THE NEXT STEP IN THE EVOLUTION OF ANTIHYPERTENSIVE THERAPY. CHEMTRACTS: ORGANIC CHEMISTRY, 1994, 6(5), 263
  148690. 284. A REVIEWa
  148691. GABRIEL WEATHERHEAD
  148692. 6582N
  148693. 2/28/96V
  148694. LOWN, J. WILLIAM. TARGETING THE DNA MINORGROOVE FOR CONTROL OF BIOLOGICAL FUNCTION: PROGRESS, CHALLENGES, AND PROSPECTS. CHEMTRACTS: ORGANIC CHEMISTRY, 1994, 6(4), 205
  148695. 237. A REVIEWa
  148696. GABRIEL WEATHERHEAD
  148697. 6583N
  148698. 2/28/96V
  148699. THIBBLIN, ALF. MECHANISMS OF SOLVOLYTIC ALKENE FORMING ELIMINATION REACTIONS. CHEMICAL SOCIETY REVIEWS, 1993, 22(6), 427
  148700. 33. A REVIEWa
  148701. GABRIEL WEATHERHEAD
  148702. 6584N
  148703. 2/28/96V
  148704. MARCUS, Y. THE PROPERTIES OF ORGANIC LIQUIDS THAT ARE RELEVANT TO THEIR USE AS SOLVATING SOLVENTS. CHEMICAL SOCIETY REVIEWS, 1993, 22(6) 409
  148705. 16. A REVIEWa
  148706. GABRIEL WEATHERHEAD
  148707. 6585N
  148708. 2/28/96V
  148709. WEBB, THOMAS H.; WILCOX, CRAIG S. ENANTIOSELECTIVE ANDDIASTEREOSELECTIVE MOLECULAR RECOGNITION OF NEUTRAL MOLECULES. CHEMICAL SOCIETY REVIEWS, 1993, 22(6), 383
  148710. 95. A REVIEWa
  148711. GABRIEL WEATHERHEAD
  148712. 6586N
  148713. 2/28/96
  148714. HOLLAS, J. MICHAEL. DETERMINATION OF MOLECULAR CONFORMATION FROM LARGE AMPLITUDE VIBRATIONS IN ELECTRONICSPECTRA OF ORGANIC MOLECULES IN A SUPERSONIC JET. CHEMICAL SOCIETY REVIEWS, 1993,22(6),371
  148715. 82. A REVIEWa
  148716. GABRIEL WEATHERHEAD
  148717. 6587N
  148718. 2/28/96VwPERUTZ, ROBIN N. ORGANOMETALLIC INTERMEDIATES: ULTIMATEREAGENTS. CHEMICAL SOCIETY REVIEWS, 1993, 22(6), 361
  148719. 9. A REVIEWa
  148720. GABRIEL WEATHERHEAD
  148721. 6588N
  148722. 2/28/96V
  148723. DAVIS, ANTHONY P. CHOLAPHANESET AL. STEROIDS ASSTRUCTURAL COMPONENTS IN MOLECULAR ENGINEERING. CHEMICAL SOCIETY REVIEWS, 1993, 22(4),243
  148724. 53. A REVIEWa
  148725. GABRIEL WEATHERHEAD
  148726. 6589N
  148727. 2/28/96V
  148728. IQBAL, JAVED; BHATIA, BEENA; NAYYAR, NARESH K. TRANSITION METAL
  148729. PROMOTED FREE
  148730. RADICAL REACTIONS IN ORGANICSYNTHESIS: THE FORMATION OF CARBON
  148731. CARBON BONDS.  CHEMICAL REVIEWS, 1994, 94(2), 519
  148732. 64. A REVIEWa
  148733. GABRIEL WEATHERHEAD
  148734. 6590N
  148735. 2/28/96
  148736. THURSTON, DAVID E.; BOSE, D. SUBHAS. SYNTHESISOF DNA
  148737. INTERACTIVE PYRROLO[2, 1 
  148738. C][ 1 ,4]BENZODIAZEPINES.  CHEMICAL REVIEWS, 1994, 94(2), 433
  148739. 65. A REVIEWa
  148740. GABRIEL WEATHERHEAD
  148741. 6591N
  148742. 2/28/96V
  148743. KIPLINGER, JAQUELINE L.; RICHMOND, THOMAS G.;OSTERBERG, CAROLYN E. ACTIVATION OF CARBON
  148744. FLUORINE BONDS BY METAL COMPLEXES.  CHEMICAL REVIEWS, 1994, 94(2), 373
  148745. 431. A REVIEWa
  148746. GABRIEL WEATHERHEAD
  148747. 6592N
  148748. 2/28/96V
  148749. MONTFORTS, FRANZ PETER; GERLACH, BENJAMIN; HOEPER, FRANK. DISCOVERY AND SYNTHESIS OF LESS COMMON NATURAL HYDROPORPHYRINS.  CHEMICAL REVIEWS, 1994, 94(2), 327
  148750. 47. A REVIEWa
  148751. GABRIEL WEATHERHEAD
  148752. 6593N
  148753. 2/28/96V
  148754. HAIDUC, I.; KING, R. B.; NEWTON, M. G. STEREOCHEMICAL ASPECTS OF TELLURIUM COMPLEXES WITH SULFUR LIGANDS: MOLECULAR COMPOUNDS AND SUPRAMOLECULAR ASSOCIATIONS.  CHEMICAL REVIEWS, 1994, 94(2), 301
  148755. 26. A REVIEWa
  148756. GABRIEL WEATHERHEAD
  148757. 6594N
  148758. 2/28/96
  148759. VAN VEGGEL, FRANK C. J. M.; VERBOOM, WILLEM; REINHOUDT, DAVID N. METALLOMACROCYCLES: SUPRAMOLECULAR CHEMISTRY WITH HARD AND SOFT METAL CATIONS IN ACTION.  CHEMICAL REVIEWS, 1994, 94(2), 279
  148760. 99. A REVIEWa
  148761. GABRIEL WEATHERHEAD
  148762. 6595N
  148763. 2/28/96V
  148764. BREDAS, J. L.; ADANT, C.; TACKX, P.; PERSOONS, A.;PIERCE, B. M. THIRD
  148765. ORDER NONLINEAR OPTICAL RESPONSE IN ORGANIC MATERIALS: THEORETICAL AND EXPERIMENTAL ASPECTS. CHEMICAL REVIEWS, 1994, 94(1), 243
  148766. 78. A REVIEWa
  148767. GABRIEL WEATHERHEAD
  148768. 6596N
  148769. 2/28/96V7SCHUBERT, ULRICH. FORMATION AND BREAKING SI
  148770. E. A REVIEWa
  148771. GABRIEL WEATHERHEAD
  148772. 6597N
  148773. 2/28/96V
  148774. BACH, T. CATALYTIC ENANTIOSELECTIVE C
  148775. C COUPLING ALLYL TRANSFER AND MUKAIYAMA ALDOL REACTION. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(4), 417
  148776. 19. A REVIEWa
  148777. GABRIEL WEATHERHEAD
  148778. 6598N
  148779. 2/28/96
  148780. JVzHOSS, R.; VOGTLE, F. TEMPLATE SYNTHESES. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(4), 375
  148781. 84. A REVIEWa
  148782. GABRIEL WEATHERHEAD
  148783. 6599N
  148784. 2/28/96V
  148785. LISKAMP, ROB M. J. A NEW APPLICATION OF MODIFIED PEPTIDES AND PEPTIDOMIMETICS: POTENTIAL ANTICANCER AGENTS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(3), 305
  148786. 7. A REVIEWa
  148787. GABRIEL WEATHERHEAD
  148788. 6600N
  148789. 2/28/96V
  148790. SCHMALZ, HANS
  148791. GUNTHER. CHROMIUM CARBENE COMPLEXES IN ORGANIC SYNTHESIS: RECENT DEVELOPMENTS AND PERSPECTIVES. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(3), 303
  148792. 5. A REVIEWa
  148793. GABRIEL WEATHERHEAD
  148794. 6601N
  148795. 2/28/96V
  148796. HERGES, RAINER. ORGANIZING PRINCIPLE OF COMPLEX REACTIONS AND THEORY OF COARCTATE TRANSITION STATES. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(3), 255
  148797. 76. A REVIEWa
  148798. GABRIEL WEATHERHEAD
  148799. 6602N
  148800. 2/28/96
  148801. AGGARWAL, VARINDER KUMAR. ENANTIOSELECTIVE TRANSFORMATIONS AND RACEMIZATION STUDIES OF HETEROATOM SUBSTITUTED ORGANOLITHIUM COMPOUNDS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(2),175
  148802.  7. A REVIEWa
  148803. GABRIEL WEATHERHEAD
  148804. 6603N
  148805. 2/28/96V
  148806. LEITNER, WALTER. A NICKEL COMPLEX FOR PHOTOCHEMICAL ACTIVATION OF CARBON DIOXIDE.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(2),173
  148807. 4. A REVIEWa
  148808. GABRIEL WEATHERHEAD
  148809. 6604N
  148810. 2/28/96V
  148811. HULLIGER, JUERG. CHEMISTRY AND CRYSTAL GROWTH.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(2), 143
  148812. 62. A REVIEWa
  148813. GABRIEL WEATHERHEAD
  148814. 6605N
  148815. 2/28/96V
  148816. REISER, OLIVIER. OXIDATION OF WEAKLY ACTIVATEDC
  148817. H BONDS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(1), 69
  148818. 72. A REVIEWa
  148819. GABRIEL WEATHERHEAD
  148820. 6606N
  148821. 2/28/96
  148822. FINK, GEORG. COOPERATIVE EFFECT IN RH2 COMPLEXES: HIGH CATALYTIC ACTIVITY AND HIGH REGIOSELECTIVITY IN THE HYDROFORMYLATION OF OLEFINS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1994, 33(1), 67
  148823. 9. A REVIEWa
  148824. GABRIEL WEATHERHEAD
  148825. 6607N
  148826. 2/28/96V
  148827. NICOLAOU, KYRIACOS COSTA; DAI, WEI
  148828. MIN; GUY, RODNEY KIPLIN. CHEMISTRY AND BIOLOGY OF TAXOL. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH. A REVIEWa
  148829. GABRIEL WEATHERHEAD
  148830. 6608N
  148831. 2/28/96V
  148832. UNVERZAGT, CARLO. A SUGAR
  148833. BASED DESIGNER DRUG AGAINST INFLUENZA? ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(12), 1691
  148834. 3. A REVIEWa
  148835. GABRIEL WEATHERHEAD
  148836. 6609N
  148837. 2/28/96V
  148838. PRAKASH, OM; SINGH, SHIV P. IODOBENZENE DIACETATE AND RELATED HYPERVALENT IODINE REAGENTS IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. ALDRICHIMICA ACTA 1994, 27(1), 1523. A REVIEWa
  148839. GABRIEL WEATHERHEAD
  148840. 6610N
  148841. 2/28/96
  148842. JUARISTI, EUSEBIO; QUINTANA, DELIA; ESCALANTE, JAIME. ENANTIOSELECTIVE SYNTHESIS OF 
  148843. AMINO ACIDS. ALDRICHIMICA ACTA 1994, 27(1), 3
  148844. 11. A REVIEWa
  148845. GABRIEL WEATHERHEAD
  148846. 6611N
  148847. 2/28/96VzJONES, J. BRYAN. PROBING THE SPECIFICITY OF SYNTHETICALLY USEFUL ENZYMES. ALDRICHIMICA ACTA 1994, 26(4), 105
  148848. 112. A REVIEWa
  148849. GABRIEL WEATHERHEAD
  148850. 6612N
  148851. 2/28/96V
  148852. TOMALIA, DONALD A. STARBURST
  148853. /CASCADE DENDRIMERS: FUNDAMENTAL BUILDING BLOCKS FOR A NEW NANOSCOPIC CHEMISTRY SET. ALDRICHIMICA ACTA 1994, 26(4), 91
  148854. 101. A REVIEWa
  148855. GABRIEL WEATHERHEAD
  148856. 6613N
  148857. 2/28/96V
  148858. BORDEN, WESTON THATCHER; IWAMURA, HIIZU;BERSON, JEROME A. VIOLATIONS OF HUND'S RULE IN NON
  148859. KEKULE HYDROCARBONS: THEORETICAL PREDICTION AND EXPERIMENTAL VERIFICATION. ACCOUNTS OF CHEMICAL RESEARCH 1994, 27(4),109
  148860. 16. A REVIEWa
  148861. GABRIEL WEATHERHEAD
  148862. 6614N
  148863. 2/28/96
  148864. PARSONS, SIMON; PASSMORE, JACK. RINGS, RADICALS, AND SYNTHETIC METALS: THE CHEMISTRY OF SNS+  .ACCOUNTS OF CHEMICAL RESEARCH 1994, 27(4), 101
  148865. 8. A REVIEWa
  148866. GABRIEL WEATHERHEAD
  148867. 6615N
  148868. 2/28/96V
  148869. GRIESBECK, AXEL G.; MAUDER, HARALD; STADTMUELLER, STEFAN. INTERSYSTEM CROSSING IN TRIPLET 1,4
  148870. BIRADICALS: CONFORMATIONAL MEMORY EFFECTS ON THE STEREOSELECTIVITY OF PHOTOCYCLOADDITION REACTIONS. ACCOUNTS OF CHEMICAL RESEARCH 1994, 27(3), 70
  148871. 5. A REVIEWa
  148872. GABRIEL WEATHERHEAD
  148873. 6616N
  148874. 2/28/96V
  148875. GERSON, FABIAN. APPLICATIONS OF ENDOR SPECTROSCOPY TO RADICAL CATIONS IN EON MATRIXES. ACCOUNTS OF CHEMICAL RESEARCH 1994, 27(3), 63
  148876. 9. A REVIEWa
  148877. GABRIEL WEATHERHEAD
  148878. 6617N
  148879. 2/28/96V
  148880. ADAM, WALDEMAR; RICHTER, MARKUS J. METAL
  148881. CATALYZED DIRECT HYDROXY
  148882. EPOXIDATION OF OLEFINS.  ACCOUNTS OF CHEMICAL RESEARCH1994, 27(2), 57
  148883. 62. A REVIEWa
  148884. GABRIEL WEATHERHEAD
  148885. 6618N
  148886. 2/28/96
  148887. SESSLER, JONATHAN L.; HEMMI, GREGORY; MODY, TARAK, D., MURAI, TOSHIAKI; BURRELL, ANTHONY; YOUNG, STUART W. TEXAPHYRINS: SYNTHESIS AND APPLICATIONS. ACCOUNTS OF CHEMICAL RESEARCH1994, 27(2), 43
  148888. 50. A REVIEWa
  148889. GABRIEL WEATHERHEAD
  148890. 6619N
  148891. 2/28/96V
  148892. PADDON
  148893. ROW, MICHAEL, N. INVESTIGATING LONG
  148894. RANGE ELECTRON
  148895. TRANSFER PROCESSES WITH RIGID, COVALENTLY LINKED DONOR
  148896. (NORBORNYLOGOUS BRIDGE)
  148897. ACCEPTOR SYSTEMS. ACCOUNTS OF CHEMICAL RESEARCH1994, 27(1), 18
  148898. 25. A REVIEWa
  148899. GABRIEL WEATHERHEAD
  148900. 6620N
  148901. 2/28/96V
  148902. POSS, CHRISTOPHER S.; SCHREIBER, STUART L. TWO
  148903. DIRECTIONAL CHAIN SYNTHESIS AND TERMINUS DIFFERENTIATION. ACCOUNTS OF CHEMICAL RESEARCH 1994, 27(1), 9
  148904. 17. A REVIEWa
  148905. GABRIEL WEATHERHEAD
  148906. ADV. HET. CHEMCKESKER, JOHN L.; NEWCOMB, M.; REVIEW, AMINYL RADICALS, PYRROLIDINE SYNTHESISM
  148907. 6621N
  148908. 2/28/96VjTHE GENERATION OF NITROGEN RADICALS AND THEIR CYCLIZATIONS FOR THE CONSTRUCTION OF THE PYRROLIDINE NUCLEUSW
  148909. 1993  58  1
  148910. GABRIEL WEATHERHEAD
  148911. Tet. Lett.CcRAWAL AZIDE ACYL ESTER CONVERSION DIETHYLALUMINUM ALUMINUM CURTIUS PREPARATION REARRANGEMENT REVIEWM
  148912. 6622N
  148913. 2/28/96VHONE STEP CONVERSION OF ESTERS TO ACYL AZIDES USING DIETHYLALUMINUM AZIDEW
  148914. 1994 P 4947a
  148915. GABRIEL WEATHERHEAD
  148916. ORG PREP PROCEDURE INTC
  148917. BERTRAND MPM
  148918. 6623N
  148919. 2/28/96VORECENT PROGRESS IN THE USE OF SULFONYL RADICALS IN ORGANIC SYNTHESIS 
  148920.  A REVIEWW
  148921. 1994 JUNX
  148922.  26(3)a
  148923. GABRIEL WEATHERHEAD
  148924. J ORG CHEMC:DIKETENE REVIEW REFERENCES ADDITIVE ALDRICH TIN DICARBONYLM
  148925. 6624N
  148926. 2/28/96V;DIKETENE 
  148927.  LEADING REFERENCES SEE BACK OF VOL 59 J ORG CHEMW
  148928. VOL 59 1994a
  148929. GABRIEL WEATHERHEAD
  148930. JACSChEVANS COPPER CATALYST AZIRIDINE AZIRIDINATION CHIRAL ASYMMETRIC NITRENOID MANGANESE SALEN REVIEW WRITINGM
  148931. 6625N
  148932. 2/28/96VADEVELOPMENT OF THE COPPER
  148933. CATALYZED OLEFIN AZIRIDINATION REACTIONW
  148934. VOL 116 1994 P 2742a
  148935. GABRIEL WEATHERHEAD
  148936. ORG PREP PROCEDURE INTC    SHIBATA IM
  148937. 6626N
  148938. 2/28/96V3ORGANOTIN ENOLATES IN ORGANIC SYNTHESIS 
  148939.  A REVIEW.W
  148940. 1994 FEBX
  148941. 26(1)a
  148942. GABRIEL WEATHERHEAD
  148943. ORG PREP PROCEDURE INTC
  148944. ALLEN AJM
  148945. 6627N
  148946. 2/28/96V2FURANOSESQUITERPENE SYNTHESIS 
  148947.  AN UPDATED REVIEW.W
  148948. 1994 FEBX
  148949. 26(1)a
  148950. GABRIEL WEATHERHEAD
  148951. 6628N
  148952. 2/28/96V
  148953. VOLODARSKY, LEONID B.; REZNIKOV, VLADIMIR A.; OVCHARENKO, VICTOR I.  SYNTHETIC CHEMISTRY OF STABLE NITROXIDES.  CRC PRESS:  BOCA RATON, FL, 1994. A REVIEWa
  148954. GABRIEL WEATHERHEAD
  148955. 6629N
  148956. 2/28/96V
  148957. THOMSON, R. C., ED. THE CHEMISTRY OF NATURAL PRODUCTS, 2ND ED. BLACKIE ACADEMIC AND PROFESSIONAL: GLASGOW, U.K., 1993. A REVIEWa
  148958. GABRIEL WEATHERHEAD
  148959. 6630N
  148960. 2/28/96VeTHEBTARANONTH, C.; THEBTARANONTH, Y. CYCLIZATION REACTIONS. CRC PRESS: BOCA RATON, FL, 1994. A REVIEWa
  148961. GABRIEL WEATHERHEAD
  148962. 6631N
  148963. 2/28/96
  148964. kVXSTOWELL, JOHN C. INTERMEDIATE ORGANIC CHEMISTRY, 2ND ED. WILEY: NEW YORK, 1993. A REVIEWa
  148965. GABRIEL WEATHERHEAD
  148966. 6632N
  148967. 2/28/96V
  148968. STONE, F. GORDON A. LEAVING NO STONE UNTURNED: PATHWAYS IN ORGANOMETALLIC CHEMISTRY (PROFILES, PATHWAYS AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS, JEFFREY I. SEEMAN, ED.). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1993. A REVIEWa
  148969. GABRIEL WEATHERHEAD
  148970. 6633N
  148971. 2/28/96V
  148972. SPLITTER, JANET S.; TURECEK, FRANTISEK. APPLICATIONS OF MASS SPECTROMETRY TO ORGANIC STEREOCHEMISTRY. VCH: NEW YORK, 1994. A REVIEWa
  148973. GABRIEL WEATHERHEAD
  148974. 6634N
  148975. 2/28/96VsPURDIE, NEIL; BRITTAIN, HARRY G. ANALYTICAL APPLICATIONS OF CIRCULAR DICHROISM. ELSEVIER: AMSTERDAM, 1994. A REVIEWa
  148976. GABRIEL WEATHERHEAD
  148977. 6635N
  148978. 2/28/96V
  148979. NORMAN, RICHARD O. C.; COXON, JAMES M. PRINCIPLES OF ORGANIC SYNTHESIS, 3RD ED. BLACKIE ACADEMIC AND PROFESSIONAL: LONDON, 1993. A REVIEWa
  148980. GABRIEL WEATHERHEAD
  148981. 6636N
  148982. 2/28/96VqMEZEY, PAUL G. SHAPE IN CHEMISTRY. AN INTRODUCTION TO MOLECULAR SHAPE AND TOPOLOGY. VCH: NEW YORK, 1993. A REVIEWa
  148983. GABRIEL WEATHERHEAD
  148984. 6637N
  148985. 2/28/96VtLEWIS, KENRICH M.; RETHWISCH, DAVID G.  CATALYZED DIRECT REACTIONS OF SILICON.  ELSEVIER:  AMSTERDAM, 1993. A REVIEWa
  148986. GABRIEL WEATHERHEAD
  148987. 6638N
  148988. 2/28/96V
  148989. LARSON, RICHARD A.; WEBER, ERIC J. REACTION MECHANISMS IN ENVIRONMENTAL ORGANIC CHEMISTRY. LEWIS PUBLISHERS: BOCA RATON, FL, 1993. A REVIEWa
  148990. GABRIEL WEATHERHEAD
  148991. 6639N
  148992. 2/28/96V
  148993. KROHN, KARSTEN K.; KIRST, HERBERT A.; MAAG, HANS. ANTIBIOTICS AND ANTIVIRAL COMPOUNDS. CHEMICAL SYNTHESIS AND MODIFICATIONS. VCH: NEW YORK, 1993. A REVIEWa
  148994. GABRIEL WEATHERHEAD
  148995. 6640N
  148996. 2/28/96V
  148997. HUDLICKY, TOMAS; CEBULAK, MARY. CYCLITOLS AND THEIR DERIVATIVES: A HANDBOOK OF PHYSICAL, SPECTRAL, AND SYNTHETIC DATA. VCH: NEW YORK, 1993. A REVIEWa
  148998. GABRIEL WEATHERHEAD
  148999. 6641N
  149000. 2/28/96
  149001. uVhFRENKEL, MICHAEL, ED. THERMOCHEMISTRY AND EQUILIBRIA OF ORGANIC COMPOUNDS. VCH: NEW YORK, 1993. A REVIEWa
  149002. GABRIEL WEATHERHEAD
  149003. 6642N
  149004. 2/28/96V
  149005. FILLER, ROBERT, ED. ORGANOFLUORINE COMPOUNDS IN MEDICINAL CHEMISTRY AND BIOMEDICAL APPLICATIONS (STUDIES IN ORGANIC CHEMISTRY, VOL. 48). ELSEVIER: AMSTERDAM, 1993 A REVIEWa
  149006. GABRIEL WEATHERHEAD
  149007. 6643N
  149008. 2/28/96VcCHAPMAN, J. R. PRACTICAL ORGANIC MASS SPECTROMETRY, 2ND ED. WILEY: CHICHESTER, U.K., 1993. A REVIEWa
  149009. GABRIEL WEATHERHEAD
  149010. 6644N
  149011. 2/28/96VcBODANSZKY, MIKLOS. PRINCIPLES OF PEPTIDE SYNTHESIS, 2ND ED. SPRINGER
  149012. VERLAG: BERLIN, 1993. A REVIEWa
  149013. GABRIEL WEATHERHEAD
  149014. 6645N
  149015. 2/28/96VkBODANSZKY, MIKLOS. PEPTIDE CHEMISTRY. A PRACTICAL TEXTBOOK, 2ND ED. SPRINGER
  149016. VERLAG: BERLIN, 1993. A REVIEWa
  149017. GABRIEL WEATHERHEAD
  149018. 6646N
  149019. 2/28/96
  149020. AGRAWAL, SUDHIR, ED. PROTOCOLS FOR OLIGONUCLEOTIDES AND ANALOGS: SYNTHESIS AND PROPERTIES (METHODS IN MOLECULAR BIOLOGY, 20). HUMANA: TOTOWA, NJ, 1993. A REVIEWa
  149021. GABRIEL WEATHERHEAD
  149022. 6647N
  149023. 2/28/96V
  149024. VAN DOORN, ARIE R.; VERBOOM, WILLEM; REINHOUDT, DAVID N. MOLECULAR RECOGNITION OF NEUTRAL MOLECULES BY SYNTHETIC RECEPTORS.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149025. GABRIEL WEATHERHEAD
  149026. 6648N
  149027. 2/28/96V
  149028. CZARNIK, ANTHONY W. FLUORESCENT CHEMOSENSORS FOR METAL AND NON
  149029. METAL IONS IN AQUEOUS SOLUTION BASED ON THE 'CHEF' PARADIGM.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149030. GABRIEL WEATHERHEAD
  149031. 6649N
  149032. 2/28/96V
  149033. SHINKAI, SEIJI. CALIXARENES AS THE THIRD SUPRAMOLECULAR HOST.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEW
  149034. GABRIEL WEATHERHEAD
  149035. 6650N
  149036. 2/28/96V
  149037. KADEN, THOMAS A. FUNCTIONALIZED TETRAAZAMACROCYCLES: LIGANDS WITH MANY ASPECTS.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149038. GABRIEL WEATHERHEAD
  149039. 6651N
  149040. 2/28/96V
  149041. TAKEMOTO, KIICHI; MIYATA, MIKIJI. INCLUSION POLYMERIZATION IN STEROIDAL CANAL COMPLEXES.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149042. GABRIEL WEATHERHEAD
  149043. 6652N
  149044. 2/28/96V
  149045. COLLET, ANDRE; DUTASTA, JEAN
  149046. PIERRE; LOZACH BENEDICT. CRYPTOPHANES: RECEPTORS FOR TETRAHEDRAL MOLECULES.  ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 3. GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149047. GABRIEL WEATHERHEAD
  149048. 6653N
  149049. 2/28/96
  149050. LUEF, WOLFGANG; KEESE, REINHART. PLANARIZING DISTORTIONS IN CARBON COMPOUNDS.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY.  VOLUME 3. BRIAN HALTON, ED., JAI PRESS: GREENWICH,  CT, 1993. A REVIEWa
  149051. GABRIEL WEATHERHEAD
  149052. 6654N
  149053. 2/28/96V
  149054. BICKELHAUPT, FRIEDRICH; DE WOLF, WILLEN. SMALL AND STRAINED CYCLOPHANES.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY.  VOLUME 3. BRIAN HALTON, ED., JAI PRESS: GREENWICH,  CT, 1993. A REVIEWa
  149055. GABRIEL WEATHERHEAD
  149056. 6655N
  149057. 2/28/96V
  149058. TODA, FIMUO. DIMETHYLENECYCLOBUTENE, BENZOCYCLOBUTADIENE, BENZODICYCLOBUTADIENE AND THEIR RELATED COMPOUNDS.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY.  VOLUME 3. BRIAN HALTON, ED., JAI PRESS: GREENWICH,  CT, 1993. A REVIEWa
  149059. GABRIEL WEATHERHEAD
  149060. 6656N
  149061. 2/28/96V
  149062. KABE, YOSHIO; ANDO, WATARU. SMALL
  149063. RING ORGANO
  149064. SILICON, GERMANIUM, AND TIN COMPOUNDS.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY.  VOLUME 3. BRIAN HALTON, ED., JAI PRESS: GREENWICH,  CT, 1993. A REVIEW
  149065. GABRIEL WEATHERHEAD
  149066. 6657N
  149067. 2/28/96V
  149068. DOLBIER, WILLIAM. THERMAL REARRANGEMENTS OF FLUORINE
  149069. CONTAINING CYCLOPROPANES.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY.  VOLUME 3. BRIAN HALTON, ED., JAI PRESS: GREENWICH,  CT, 1993. A REVIEWa
  149070. GABRIEL WEATHERHEAD
  149071. 6658N
  149072. 2/28/96V
  149073. GUENGERICH, F. PETER; MACDONALD, TIMOTHY L. SEQUENTIAL ELECTRON TRANSFER REACTIONS CATALYZED BY CYTOCHROME P
  149074. 450 ENZYMES.  ADVANCES IN ELECTRON TRANSFER CHEMISTRY. VOLUME 3. PATRICK S. MARIANO, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149075. GABRIEL WEATHERHEAD
  149076. 6659N
  149077. 2/28/96V
  149078. NELSEN, STEPHEN F. INTERNAL GEOMETRY RELAXATION EFFECTS ON ELECTRON TRANSFER RATES OF AMINO CENTERED SYSTEMS.  ADVANCES IN ELECTRON TRANSFER CHEMISTRY. VOLUME 3. PATRICK S. MARIANO, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149079. GABRIEL WEATHERHEAD
  149080. 6660N
  149081. 2/28/96
  149082. SERPONE, NICK; TERZIAN, RITA; LAWLESS, DARREN; HERRMANN, JEAN
  149083. MARIE. LIGHT
  149084. INDUCED ELECTRON TRANSFER IN INORGANIC SYSTEMS IN HOMOGENEOUS AND HETEROGENEOUS PHASES.  ADVANCES IN ELECTRON TRANSFER CHEMISTRY. VOLUME 3. PATRICK S. MARIANO, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEW
  149085. GABRIEL WEATHERHEAD
  149086. 6661N
  149087. 2/28/96V
  149088. JONES, GUILFORD, II; FARAHAT, MOHAMMAD S. PHOTOINDUCED ELECTRON TRANSFER IN FLEXIBLE BIARYL DONOR
  149089. ACCEPTOR MOLECULES.  ADVANCES IN ELECTRON TRANSFER CHEMISTRY. VOLUME 3. PATRICK S. MARIANO, ED., JAI PRESS: GREENWICH, CT, 1993. A REVIEWa
  149090. GABRIEL WEATHERHEAD
  149091. 6662N
  149092. 2/28/96V
  149093. GERWICK, WILLIAM H.; NAGLE, DALE G.; PROTEAU, PHILIP J. OXYLIPINS FROM MARINE INVERTEBRATES. TOPICS IN CURRENT CHEMISTRY 1993,167 (MARINE NATURAL PRODUCTS
  149094. DIVERSITY AND BIOSYNTHESIS), 117
  149095. 80. A REVIEWa
  149096. GABRIEL WEATHERHEAD
  149097. 6663N
  149098. 2/28/96
  149099. CIMINO, GUIDO; SODANO, GUIDO. BIOSYNTHESIS OF SECONDARY METABOLITES IN MARINE MOLLUSCS. TOPICS IN CURRENT CHEMISTRY 1993,167 (MARINE NATURAL PRODUCTS
  149100. DIVERSITY AND BIOSYNTHESIS), 77
  149101. 115. A REVIEWa
  149102. GABRIEL WEATHERHEAD
  149103. 6664N
  149104. 2/28/96V
  149105. CHANG, CLIFFORD W. J. MARINE ISOCYANO COMPOUNDS. TOPICS IN CURRENT CHEMISTRY 1993,167 (MARINE NATURAL PRODUCTS
  149106. DIVERSITY AND BIOSYNTHESIS), 33
  149107. 75. A REVIEWa
  149108. GABRIEL WEATHERHEAD
  149109. 6665N
  149110. 2/28/96V
  149111. BAKER, BILL J.; KERR, RUSSELL G. BIOSYNTHESIS OF MARINE STEROLS. TOPICS IN CURRENT CHEMISTRY 1993,167 (MARINE NATURAL PRODUCTS DIVERSITY AND BIOSYNTHESIS), 1
  149112. 31. A REVIEWa
  149113. GABRIEL WEATHERHEAD
  149114. 6666N
  149115. 2/28/96V
  149116. LLOYD
  149117. WILLIAMS, PAUL; ALBERICIO, FERNANDO; GIRALT, ERNEST. CONVERGENT SOLID
  149118. PHASE PEPTIDE SYNTHESIS. TETRAHEDRON 1993, 49(48), 11065
  149119. 133. A REVIEWa
  149120. GABRIEL WEATHERHEAD
  149121. 6667N
  149122. 2/28/96
  149123. V{ROXBURGH, CRAIG J. SYNTHESES OF MEDIUM SIZED RINGS BY RING EXPANSION REACTIONS. TETRAHEDRON 1993, 49(47),10749
  149124. 84. A REVIEWa
  149125. GABRIEL WEATHERHEAD
  149126. 6668N
  149127. 2/28/96V
  149128. BEAUCAGE, SERGE L.; IYER, RADHAKRISHNAN P. THE SYNTHESIS OF SPECIFIC RIBONUCLEOTIDES AND UNRELATED PHOSPHORYLATED BIOMOLECULES BY THE PHOSPHORAMIDITE METHOD. TETRAHEDRON 1993, 49(46), 10441
  149129. 88. A REVIEWa
  149130. GABRIEL WEATHERHEAD
  149131. 6669N
  149132. 2/28/96
  149133. SCHLOSSER, MANFRED; DESPONDS, OLIVIER; LEHMANN, RUTH; MORET, ETIENNE; RAUCHSCHWALBE, GUNTER. POLAR ALLYL TYPE ORGANOMETALLICS AS KEY INTERMEDIATES IN REGIO
  149134.  AND STEREOCONTROLLED REACTIONS: CONFORMATIONAL MOBILITIES.  TETRAHEDRON 1993, 49(45), 10175
  149135. 203. A REVIEW
  149136. GABRIEL WEATHERHEAD
  149137. 6670N
  149138. 2/28/96V
  149139. WNUK, STANISLAW F. SULFUR
  149140.  AND SELENO
  149141. SUGAR MODIFIED NUCLEOSIDES. SYNTHESIS, CHEMICAL TRANSFORMATIONS AND BIOLOGICAL PROPERTIES. TETRAHEDRON 1993, 49(44), 9877
  149142. 936. A REVIEWa
  149143. GABRIEL WEATHERHEAD
  149144. 6671N
  149145. 2/28/96V
  149146. NIYAZYMBETOV, MURAT E.; EVANS, DENNIS H. THE UTILITY OF CARBANIONS AND HETEROATOM
  149147. ANIONS IN ELECTRO
  149148. ORGANIC SYNTHESIS. TETRAHEDRON 1993, 49(43), 9627
  149149. 88. A REVIEWa
  149150. GABRIEL WEATHERHEAD
  149151. 6672N
  149152. 2/28/96VzRESNATI, GIUSEPPE. SYNTHESIS OF CHIRAL AND BIOACTIVE FLUOROORGANIC COMPOUNDS. TETRAHEDRON 1993, 49(42), 9385
  149153. 445. A REVIEWa
  149154. GABRIEL WEATHERHEAD
  149155. 6673N
  149156. 2/28/96VoSHINKAI, SEIJI. CALIXARENES
  149157. THE THIRD GENERATION OF SUPRAMOLECULES. TETRAHEDRON 1993, 49(40), 8933
  149158. 68. A REVIEWa
  149159. GABRIEL WEATHERHEAD
  149160. 6674N
  149161. 2/28/96V
  149162. DALE, JOHANNES. THE CONTRASTING BEHAVIOR OF OXIRANE AND OXETANE IN CATIONIC CYCLOOLOGOMERIZATION AND POLYMERIZATION. TETRAHEDRON 1993, 49(39), 8707
  149163. 25. A REVIEWa
  149164. GABRIEL WEATHERHEAD
  149165. 6675N
  149166. 2/28/96V
  149167. FERINGA, BEN L.; JAGER, WOLTER F.; DE LANGE, BEN. ORGANIC MATERIALS FOR REVERSIBLE OPTICAL STORAGE. TETRAHEDRON 1993, 49(37), 8267
  149168. 310. A REVIEWa
  149169. GABRIEL WEATHERHEAD
  149170. 6676N
  149171. 2/28/96V
  149172. NISHIGAICHI, YUTAKA; TAKUWA, AKIO; NARUTA, YOSHINORI; MARUYAMA, KAZUHIRO. VERSATILE ROLES OF LEWIS ACIDS IN THE REACTIONS OF ALLYLIC TIN COMPOUNDS. TETRAHEDRON 1993, 49(34), 7395
  149173. 426. A REVIEWa
  149174. GABRIEL WEATHERHEAD
  149175. 6677N
  149176. 2/28/96VsKAPPE, C. OLIVER. 100 YEARS OF THE BIGINELLI DIHYDROPYRIDINE SYNTHESIS. TETRAHEDRON 1993, 49(32), 6937
  149177. 63. A REVIEWa
  149178. GABRIEL WEATHERHEAD
  149179. 6678N
  149180. 2/28/96V
  149181. BEAUCAGE, SERGE L.; IYER, RADHAKRISHNAN P. THE SYNTHESIS OF MODIFIED OLIGONUCLEOTIDES BY THE PHOSPHORAMIDITE APPROACH AND THEIR APPLICATIONS. TETRAHEDRON 1993, 49(28), 6123
  149182. 94. A REVIEWa
  149183. GABRIEL WEATHERHEAD
  149184. 6679N
  149185. 2/28/96V
  149186. AGER, DAVID J.; EAST, MICHAEL B. THE SYNTHESIS OF CARBOHYDRATE DERIVATIVES FROM ACYCLIC PRECURSORS. TETRAHEDRON 1993, 49(26), 5683
  149187. 765. A REVIEWa
  149188. GABRIEL WEATHERHEAD
  149189. 6680N
  149190. 2/28/96
  149191. VrMELIKYAN, GAGIK G. MANGANESE(III) MEDIATED REACTIONS OF UNSATURATED SYSTEMS. SYNTHESIS 1993, (9), 833
  149192. 50. A REVIEWa
  149193. GABRIEL WEATHERHEAD
  149194. 6681N
  149195. 2/28/96VjRITTER, KURT. SYNTHETIC TRANSFORMATIONS OF VINYL AND ARYL TRIFLATES. SYNTHESIS 1993, (8), 735
  149196. 62. A REVIEWa
  149197. GABRIEL WEATHERHEAD
  149198. 6682N
  149199. 2/28/96V
  149200. SCHUCHARDT, ULF; CARVALHO, WAGNER ALVES; SPINACE, ESTEVAM VITORIO. WHY IS IT INTERESTING TO STUDY CYCLOHEXANE OXIDATION? SYNLETT 1993, (10), 713
  149201. 18. A REVIEWa
  149202. GABRIEL WEATHERHEAD
  149203. 6683N
  149204. 2/28/96VtVARMA, RAJENDER S. SYNTHESIS OF OLIGONUCLEOTIDE ANALOGS WITH MODIFIED BACKBONES. SYNLETT 1993, (9), 621
  149205. 37. A REVIEWa
  149206. GABRIEL WEATHERHEAD
  149207. 6684N
  149208. 2/28/96V
  149209. KRAKOWIAK, KRYZSZTOF E.; BRADSHAW, JERALD S.; IZATT, REED M. IMPROVED METHODS FOR THE SYNTHESIS OF AZA
  149210. CROWN MACROCYCLES AND CRYPTANDS. SYNLETT 1993, (9), 611
  149211. 20. A REVIEWa
  149212. GABRIEL WEATHERHEAD
  149213. 6685N
  149214. 2/28/96
  149215. MCCOMBIE, STUART W.; ORTIZ, CLAUDIO; COX, BRIAN; GANGULY, ASHIT K. CONTROLLING BENZYLIC AND ANOMERIC FUNCTIONALITY AND STEREOCHEMISTRY: METHODOLOGY AND SYNTHESES UTILIZING INTRAMOLECULAR IONIC HYDROGENATION.  SYNLETT 1993, (8), 541
  149216. 7. A REVIEWa
  149217. GABRIEL WEATHERHEAD
  149218. 6686N
  149219. 2/28/96V
  149220. BARANOVSKII, A. B.; LITVINOVSKAYA, R. P.; KHRIPACH, V. A. STEROIDS WITH A SIDE CHAIN CONTAINING A HETEROCYCLIC FRAGMENT: SYNTHESIS AND TRANSFORMATIONS. RUSSIAN CHEMICAL REVIEWS 1993, 62(7), 661. A REVIEWa
  149221. GABRIEL WEATHERHEAD
  149222. 6687N
  149223. 2/28/96V
  149224. ZOLOTUKHINA, M. M.; KRUTIKOV, V. I.; LAVRENT'EV, A. N. DERIVATIVES OF DIPHOSPHONIC ACIDS: SYNTHESIS AND BIOLOGICAL ACTIVITY. RUSSIAN CHEMICAL REVIEWS 1993, 62(7), 647. A REVIEWa
  149225. GABRIEL WEATHERHEAD
  149226. 6688N
  149227. 2/28/96V|TOLSTIKOV, A. G.; TOLSTIKOV, G. A. GLYCALS IN ENANTIOSPECIFIC SYNTHESIS. RUSSIAN CHEMICAL REVIEWS 1993, 62(6), 579. A REVIEWa
  149228. GABRIEL WEATHERHEAD
  149229. 6689N
  149230. 2/28/96
  149231. ANDREEV, V. G.; KOLOMIETS, A. F. [3,3]
  149232. SIGMATROPIC REARRANGEMENTS AS A METHOD OF ORGANOFLUORINE SYNTHESIS RUSSIAN CHEMICAL REVIEWS 1993, 62(6), 553. A REVIEWa
  149233. GABRIEL WEATHERHEAD
  149234. 6690N
  149235. 2/28/96V
  149236. BARASHKOV, N. N.; SAKHNO, T. V.; NURMUKHAMETOV, R. N.; KHAKHEL', O. A. EXCIMERS OF ORGANIC MOLECULES. RUSSIAN CHEMICAL REVIEWS 1993, 62(6), 539. A REVIEWa
  149237. GABRIEL WEATHERHEAD
  149238. 6691N
  149239. 2/28/96V
  149240. KOZHEVNIKOV, I. V. FINE ORGANIC SYNTHESIS WITH THE AID OF HETEROPOLYCOMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1993, 62(5), 473. A REVIEWa
  149241. GABRIEL WEATHERHEAD
  149242. 6692N
  149243. 2/28/96V
  149244. SHAPIRO, E. A.; DYATKIN, A. B.; NEFEDOV, O. M. CARBENE REACTIONS OF DIAZOESTERS WITH O
  149245. BONDS AS AN EFFECTIVE METHOD FOR THE ALKOXYCARBONYLMETHYLENATION OF ORGANIC COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1993, 62(5), 447. A REVIEWa
  149246. GABRIEL WEATHERHEAD
  149247. 6693N
  149248. 2/28/96
  149249. SOKOLOV, V. I.; STANKEVICH, I. V. THE FULLERENES
  149250. NEW ALLOTROPIC FORMS OF CARBON: MOLECULAR AND ELECTRONIC STRUCTURE, AND CHEMICAL PROPERTIES. RUSSIAN CHEMICAL REVIEWS 1993, 62(5), 419. A REVIEWa
  149251. GABRIEL WEATHERHEAD
  149252. 6694N
  149253. 2/28/96V
  149254. CZESKIS, B. A.; IVANOVA, N. M.; MOISEENKOV, A. M.; NEFEDOV, O. M. THE CHEMISTRY OF ACETYLCYCLOPROPANE. RUSSIAN CHEMICAL REVIEWS 1993, 62(4), 337. A REVIEWa
  149255. GABRIEL WEATHERHEAD
  149256. 6695N
  149257. 2/28/96V
  149258. GRABOWSKI, ZBIGNIEW R. ELECTRON TRANSFER IN FLEXIBLE MOLECULES AND MOLECULAR IONS. PURE AND APPLIED CHEMISTRY 1993, 65(8),1751
  149259. 6. A REVIEWa
  149260. GABRIEL WEATHERHEAD
  149261. 6696N
  149262. 2/28/96V
  149263. ZACHARIASSE, KLAAS A.; VON DER HAAR, THOMAS; HEBECKER, AXEL; LEINHOS, UWE; KUEHNLE, WOLFGANG. INTRAMOLECULAR CHARGE TRANSFER IN AMINOBENZONITRILES: REQUIREMENTS FOR DUAL FLUORESCENCE. PURE AND APPLIED CHEMISTRY 1993, 65(8),1745
  149264. 50. A REVIEWa
  149265. GABRIEL WEATHERHEAD
  149266. 6697N
  149267. 2/28/96
  149268. GHONEIM, NAGWA; SUPPAN, PAUL. SOLVATION OF TICT STATES IN SOLVENT MIXTURES. PURE AND APPLIED CHEMISTRY 1993, 65(8),1739
  149269. 43.  A REVIEWa
  149270. GABRIEL WEATHERHEAD
  149271. 6698N
  149272. 2/28/96V
  149273. WORTMANN, RUEDIGER; SCHMITTGEN, RALF; DETZER, NORBERT. PHOTOINDUCED CHARGE SEPARATION AND BROKEN SYMMETRY IN FRANCK
  149274. CONDON EXCITED PI PI'* STATES OF TETRAPHENYL PENTATETRAENES. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1733
  149275. 8. A REVIEWa
  149276. GABRIEL WEATHERHEAD
  149277. 6699N
  149278. 2/28/96V
  149279. BAUMANN, WOLFRAM; NAGY, ZSOLT. PHOTOINDUCED CHARGE TRANSFER AS REVEALED BY GROUND AND EXCITED STATE DIPOLE MOMENTS. PURE AND APPLIED CHEMISTRY 1993, 65(8),1729
  149280. 32. A REVIEWa
  149281. GABRIEL WEATHERHEAD
  149282. 6700N
  149283. 2/28/96
  149284. CWARMAN, JOHN M.; JONKER, STEPHAN A.; SCHUDDEBOOM, WOUTER; DE HAAS, MATTHIJS P.; PADDON
  149285. ROW, MICHAEL N.; VERHOEVEN, JAN W.; ZACHARIASSE, KLAAS A. STRAIGHT, BENT AND TWISTED INTRAMOLECULAR CHARGE SEPARATED STATES AS SEEN BY TIME
  149286. RESOLVED MICROWAVE CONDUCTIVITY (TRMC). PURE AND APPLIED CHEMISTRY 1993, 65(8), 1723
  149287. 8. A REVIEW
  149288. GABRIEL WEATHERHEAD
  149289. 6701N
  149290. 2/28/96V
  149291. VERHOEVEN, J. W.; SCHERER, T.; WILLEMSE, R. J. SOLVENT EFFECTS ON THE STRUCTURE OF FLUORESCENT EXCIPLEXES IN RIGIDLY, FLEXIBLY, AND NONBRIDGED DONOR
  149292. ACCEPTOR SYSTEMS. PURE AND APPLIED CHEMISTRY 1993, 65(8),1717
  149293. 22. A REVIEWa
  149294. GABRIEL WEATHERHEAD
  149295. 6702N
  149296. 2/28/96V
  149297. FOX, MARYE ANNE; SUN, YA PING. EXPERIMENTAL PROBES OF EXCITED STATE CHARACTER IN SUPERCRITICAL FLUIDS. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1713
  149298. 16. A REVIEWa
  149299. GABRIEL WEATHERHEAD
  149300. 6703N
  149301. 2/28/96
  149302. ROOS, BJOERN O.; SERRANO, ANDRES LUIS; MERCHAN, MANUELA. MULTICONFIGURATIONAL SECOND ORDER PERTURBATION THEORY APPLIED TO THE CALCULATION OF ELECTRONIC SPECTRA OF CONJUGATED SYSTEMS. PURE AND APPLIED CHEMISTRY 1993, 65(8),1693
  149303. 8. A REVIEWa
  149304. GABRIEL WEATHERHEAD
  149305. 6704N
  149306. 2/28/96V
  149307. JOHNSON, ALAN E.; TOMINAGA, KEISUKE; WALKER, GILBERT C.; JARZEBA, WLODZIMIERZ; BARBARA, PAUL F. FEMTOSECOND ELECTRON TRANSFER: EXPERIMENT AND THEORY. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1677
  149308. 80. A REVIEWa
  149309. GABRIEL WEATHERHEAD
  149310. 6705N
  149311. 2/28/96
  149312. VAN DER AUWERAER, M.; DE SCHRYVER, F. C.; VERBEEK, G.; VAES, A.; HELSEN, N.; VAN HAVER, P.; DEPAEMELAERE, S.; TERRELL, D.; DE MEUTTER, S. PHOTOINDUCED ELECTRON TRANSFER IN POLYCHROMOPHORIC SYSTEMS. PURE AND APPLIED CHEMISTRY, 1993, 65(8), 1665
  149313. 70. A REVIEW
  149314. GABRIEL WEATHERHEAD
  149315. 6706N
  149316. 2/28/96
  149317. LIM, EDWARD C. PHOTOASSOCIATION IN THE LOWEST TRIPLET STATE OF AROMATIC MOLECULES: TRIPLET EXCIMERS AND EXCIPLEXES. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1659
  149318. 64. A REVIEWa
  149319. GABRIEL WEATHERHEAD
  149320. 6707N
  149321. 2/28/96V
  149322. KOEHLER, GOTTFRIED; RECHTHALER, KARL. SOLVENT EFFECTS ON EXCITED STATE RELAXATION PHENOMENA. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1647
  149323. 52. A REVIEWa
  149324. GABRIEL WEATHERHEAD
  149325. 6708N
  149326. 2/28/96VwKASHA, M.; SYTNIK, A.; DELLINGER, B. SOLVENT CAGE SPECTROSCOPY. PURE AND APPLIED CHEMISTRY 1993, 65(8),1641
  149327. 6. A REVIEWa
  149328. GABRIEL WEATHERHEAD
  149329. 6709N
  149330. 2/28/96V
  149331. SHIZUKA, HARUO. INTRAMOLECULAR CHARGE TRANSFER EMISSION FROM EXCITED PHENYLDISILANES WITHOUT TWISTED INTRAMOLECULAR CHARGE TRANSFER (TICT). PURE AND APPLIED CHEMISTRY 1993, 65(8),1635
  149332. 40. A REVIEWa
  149333. GABRIEL WEATHERHEAD
  149334. 6710N
  149335. 2/28/96
  149336. ITOH, MICHIYA. FLUORESCENCE STUDIES OF THE EXCITED
  149337. STATE PROTON TRANSFER IN SUBSTITUTED 3
  149338. HYDROXYCHROMONES IN SUPERSONIC JET. PURE AND APPLIED CHEMISTRY 1993, 65(8),1629
  149339. 34. A REVIEWa
  149340. GABRIEL WEATHERHEAD
  149341. 6711N
  149342. 2/28/96V
  149343. KENSY, UWE; GRELLMANN, KARL HEINZ; MOSQUERA, GONZALEZ MANUEL. COMPETITION BETWEEN TUNNEL AND VISCOSITY EFFECTS ON BIMOLECULAR HYDROGEN
  149344. TRANSFER REACTION. PURE AND APPLIED CHEMISTRY 1993, 65(8), 1625
  149345. 8. A REVIEWa
  149346. GABRIEL WEATHERHEAD
  149347. 6712N
  149348. 2/28/96V
  149349. MATAGA, NOBORU. PHOTOINDUCED ELECTRON TRANSFER AND MULTIPLE STATES MECHANISMS. PURE AND APPLIED CHEMISTRY 1993, 65(8),1605
  149350. 10. A REVIEWa
  149351. GABRIEL WEATHERHEAD
  149352. 6713N
  149353. 2/28/96
  149354. ZCOSTAMAGNA, JUAN; CANALES, JUAN; VARGAS, JUAN; CAMALLI, MERCEDES; CARUSO, FRANCESCO; RIVAROLA, ELEANORA. PRECURSORS OF AZA
  149355. MACROCYCLES: CHARACTERIZATION OF SUBSTITUTED PHENANTHROLINES AND RELATED BASES. CRYSTAL AND MOLECULAR STRUCTURE OF DICHLORODI
  149356. BUTYL(2,2',6,6'
  149357. BIPYRIMIDINE)
  149358. TIN(IV). PURE AND APPLIED CHEMISTRY 1993, 65(7), 1521
  149359. 6. A REVIEW
  149360. GABRIEL WEATHERHEAD
  149361. 6714N
  149362. 2/28/96V
  149363. VINCENTI, MARCO; PELIZZETTI, EZIO; DALCANALE, ENRICO SONCINI, PAOLO. MOLECULAR RECOGNITION IN THE GAS PHASE. PURE AND APPLIED CHEMISTRY 1993, 65(7), 1507
  149364. 12. A REVIEWa
  149365. GABRIEL WEATHERHEAD
  149366. 6715N
  149367. 2/28/96V
  149368. ATWOOD, JERRY L.; ORR, G. WILLIAM; JUNEJA, RAVINDAR K.; BOTT, SIMON G.; HAMADA, FUMIO. SUPRAMOLECULAR ASSEMBLIES BASED ON CALIXARENES. PURE AND APPLIED CHEMISTRY 1993, 65(7),1471
  149369. 6. A REVIEWa
  149370. GABRIEL WEATHERHEAD
  149371. 6716N
  149372. 2/28/96V^FAULKNER, D. J. MARINE NATURAL PRODUCTS. NATURAL PRODUCT REPORTS 1993, 10(5),497
  149373. 539. A REVIEW
  149374. GABRIEL WEATHERHEAD
  149375. 6717N
  149376. 2/28/96V[ROBINS, D. J. PYRROLIZIDINE ALKALOIDS. NATURAL PRODUCT REPORTS 1993,10(5), 487
  149377. 96. A REVIEWa
  149378. GABRIEL WEATHERHEAD
  149379. 6718N
  149380. 2/28/96VZYUNUSOV, M. S. DITERPENOID ALKALOIDS. NATURAL PRODUCT REPORTS 1993,10(5), 471
  149381. 86. A REVIEWa
  149382. GABRIEL WEATHERHEAD
  149383. 6719N
  149384. 2/28/96V{BENTLEY, K. W., BETA
  149385. PHENYLETHYLAMINES AND THE ISOQUINOLINE ALKALOIDS. NATURAL PRODUCT REPORTS 1993,10(5), 449
  149386. 70. A REVIEWa
  149387. GABRIEL WEATHERHEAD
  149388. 6720N
  149389. 2/28/96V^GROVE, J. F. MACROCYCLIC TRICHOTHECENES. NATURAL PRODUCT REPORTS 1993, 10(5), 429
  149390. 48. A REVIEWa
  149391. GABRIEL WEATHERHEAD
  149392. 6721N
  149393. 2/28/96V
  149394. EDMONDS, J. S.; FRANCESCONI, K. A.; STICK, R. V. ARSENIC COMPOUNDS FROM MARINE ORGANISMS. NATURAL PRODUCT REPORTS 1993,10(4), 421
  149395. 8. A REVIEWa
  149396. GABRIEL WEATHERHEAD
  149397. 6722N
  149398. 2/28/96
  149399. V[FRAGA, B. M. NATURAL SESQUITERPENOIDS. NATURAL PRODUCT REPORTS 1993,10(4),397
  149400. 419. A REVIEWa
  149401. GABRIEL WEATHERHEAD
  149402. 6723N
  149403. 2/28/96V
  149404. SAXTON, J. E. RECENT PROGRESS IN THE CHEMISTRY OF INDOLE ALKALOIDS AND MOLD METABOLITES. NATURAL PRODUCT REPORTS 1993,10(4), 349
  149405. 95. A REVIEWa
  149406. GABRIEL WEATHERHEAD
  149407. 6724N
  149408. 2/28/96VcHARBORNE, J. B. ADVANCES IN CHEMICAL ECOLOGY. NATURAL PRODUCT REPORTS 1993, 10(4), 327
  149409. 48. A REVIEWa
  149410. GABRIEL WEATHERHEAD
  149411. 6725N
  149412. 2/28/96VSHANSON, J. R. STEROID REACTIONS AND PARTIAL SYNTHESIS. 1993,10(4), 313
  149413. 25. A REVIEWa
  149414. GABRIEL WEATHERHEAD
  149415. 6726N
  149416. 2/28/96V
  149417. HANSON, J. R.; DE OLIVEIRA, B. H. STEVIOSIDE AND RELATED SWEET DITERPENOID GLYCOSIDES. NATURAL PRODUCT REPORTS 1993,10(3), 301
  149418. 9. A REVIEWa
  149419. GABRIEL WEATHERHEAD
  149420. 6727N
  149421. 2/28/96VUDEWICK, P. M. THE BIOSYNTHESIS OF SHIKIMATE METABOLITES. 1993,10(3), 233
  149422. 63. A REVIEWa
  149423. GABRIEL WEATHERHEAD
  149424. 6728N
  149425. 2/28/96V
  149426. ALPEGIANI, MARCO; BISSOLINO, PIERLUIGI; BORGHI, DANIELA; SBRALETTA, PIETRO; TONANI, ROBERTO; PERRONE, ETTORE.  FUNCTIONALIZATION OF THE DIHYDROTHIAZINE RING OF CEPHEM SULFONES.  HETEROCYCLES, 1993, 36(8), 1747
  149427. 62. A REVIEWa
  149428. GABRIEL WEATHERHEAD
  149429. 6729N
  149430. 2/28/96V
  149431. GOSWAMI, SHYAMAPROSAD. MOLYBDENUM COFACTOR: ITS BIOLOGICAL SIGNIFICANCE, STRUCTURAL, AND SYNTHETIC ASPECTS. HETEROCYCLES 1993, 35(2), 1551
  149432. 70. A REVIEWa
  149433. GABRIEL WEATHERHEAD
  149434. 6730N
  149435. 2/28/96V
  149436. DURUCASU, INCI. THE CHEMISTRY OF DDATHF (5,10
  149437. DIDEAZA
  149438. 5,6,7,8
  149439. TETRA HYDROFOLIC ACID) AS ANTITUMOR AGENT. HETEROCYCLES 1993, 35(2), 1527
  149440. 49. A REVIEWa
  149441. GABRIEL WEATHERHEAD
  149442. 6731N
  149443. 2/28/96VuITOKAWA, HIDEJI; TAKEYA, KOICHI. ANTITUMOR SUBSTANCES FROM HIGHER PLANTS. HETEROCYCLES 1993, 35(2),1467
  149444. 501. A REVIEWa
  149445. GABRIEL WEATHERHEAD
  149446. 6732N
  149447. 2/28/96
  149448. STADLBAUER, WOLFGANG; KAPPE, THOMAS. SIMPLE AND EFFECTIVE APPROACHES TO COUMESTANS AND AZACOUMESTANS. HETEROCYCLES 1993, 35(2), 1425
  149449. 40. A REVIEWa
  149450. GABRIEL WEATHERHEAD
  149451. 6733N
  149452. 2/28/96V
  149453. STAUBER, MARGARET J.; DEBIAK
  149454. KROOK, THERESE; MILLER, MARVIN J. ALKYLATION OF AMBIDENT NUCLEOPHILIC HYDROXAMATES WITH 4
  149455. SUBSTITUTED 2
  149456. AZETIDINONES: FORMATION OF BICYCLIC 
  149457. LACTAM INTERMEDIATES. HETEROCYCLES 1993, 35(2),1205
  149458. 35. A REVIEWa
  149459. GABRIEL WEATHERHEAD
  149460. 6734N
  149461. 2/28/96V
  149462. TESTA, BERNARD; CARRUPT, PIERRE
  149463. ALAIN; GAL, JOSEPH. THE SO
  149464. CALLED "INTERCONVERSION" OF STEREOISOMERIC DRUGS: AN ATTEMPT AT CLARIFICATION. CHIRALITY 1993, 5(3),105
  149465. 11. A REVIEWa
  149466. GABRIEL WEATHERHEAD
  149467. 6735N
  149468. 2/28/96V
  149469. GASPARRINI, F.; MISITI, D.; VILLANI, C. CHROMATOGRAPHIC OPTICAL RESOLUTION ON TRANS
  149470. DIAMINOCYCLOHEXANE DERIVATIVES: THEORY AND APPLICATIONS. CHIRALITY 1992, 4(7), 447
  149471. 58. A REVIEWa
  149472. GABRIEL WEATHERHEAD
  149473. 6736N
  149474. 2/28/96
  149475. MANNSCHRECK, ALBRECHT. CHIROPTICAL DETECTION DURING LIQUID CHROMATOGRAPHY: PART 4. APPLICATIONS TO STEREOANALYSIS AND STEREODYNAMICS. CHIRALITY 1992, 4(3),163
  149476. 9. A REVIEWa
  149477. GABRIEL WEATHERHEAD
  149478. 6737N
  149479. 2/28/96V
  149480. SALVADORI, PIERO; PINI, DARIO; ROSINI, CARLO; BERTUCCI, CARLO; UCCELLO
  149481. BARRETTA, GLORIA. CHIRAL DISCRIMINATIONS WITH CINCHONA ALKALOIDS. CHIRALITY 1992, 4(1), 43
  149482. 9. A REVIEWa
  149483. GABRIEL WEATHERHEAD
  149484. 6738N
  149485. 2/28/96V
  149486. NONHEBEL, DEREK C. THE CHEMISTRY OF CYCLOPROPYLMETHYL AND RELATED RADICALS. CHEMICAL SOCIETY REVIEWS 1993, 22(5), 347
  149487. 59. A REVIEWa
  149488. GABRIEL WEATHERHEAD
  149489. 6739N
  149490. 2/28/96V
  149491. CACCIAPAGLIA, R.; MANDOLINI, L. CATALYSIS BY METAL IONS IN REACTIONS OF CROWN ETHER SUBSTRATES. CHEMICAL SOCIETY REVIEWS 1993, 22(4), 221
  149492. 31. A REVIEWa
  149493. GABRIEL WEATHERHEAD
  149494. 6740N
  149495. 2/28/96VkSPERANZA, MAURIZIO. TRITIUM FOR GENERATION OF CARBOCATIONS. CHEMICAL REVIEWS 1993, 93(8), 2933
  149496. 80. A REVIEW
  149497. GABRIEL WEATHERHEAD
  149498. 6741N
  149499. 2/28/96V
  149500. FERRIER, ROBERT J.; MIDDLETON, SYDNEY. THE CONVERSION OF CARBOHYDRATE DERIVATIVES INTO FUNCTIONALIZED CYCLOHEXANES AND CYCLOPENTANES. CHEMICAL REVIEWS 1993, 93(8), 2779
  149501. 831. A REVIEWa
  149502. GABRIEL WEATHERHEAD
  149503. 6742N
  149504. 2/28/96V
  149505. SHAWALI, AHMAD SAMI. REACTIONS OF HETEROCYCLIC COMPOUNDS WITH NITRILIMINES AND THEIR PRECURSORS. CHEMICAL REVIEWS 1993, 93(8), 2731
  149506. 77. A REVIEWa
  149507. GABRIEL WEATHERHEAD
  149508. 6743N
  149509. 2/28/96V
  149510. BRILL, THOMAS B.; JAMES, KENNETH J. KINETICS AND MECHANISMS OF THERMAL DECOMPOSITION OF NITROAROMATIC EXPLOSIVES. CHEMICAL REVIEWS 1993, 93(8), 2667
  149511. 92. A REVIEWa
  149512. GABRIEL WEATHERHEAD
  149513. 6744N
  149514. 2/28/96V
  149515. SADOWSKI, JENS; GASTEIGER, JOHANN. FROM ATOMS AND BONDS TO THREE
  149516. DIMENSIONAL ATOMIC COORDINATES: AUTOMATIC MODEL BUILDERS. CHEMICAL REVIEWS 1993, 93(7), 2567
  149517. 81. A REVIEWa
  149518. GABRIEL WEATHERHEAD
  149519. 6745N
  149520. 2/28/96
  149521. MARLOW, GAIL E.; PERKYNS, JOHN S.; PETTITT, B. MONTGOMERY. SALT EFFECTS IN PEPTIDE SOLUTIONS: THEORY AND SIMULATIONS. CHEMICAL REVIEWS 1993, 93(7), 2503
  149522. 21. A REVIEWa
  149523. GABRIEL WEATHERHEAD
  149524. 6746N
  149525. 2/28/96V
  149526. BROOKS, CHARLES, III; CASE, DAVID A. SIMULATIONS OF PEPTIDE CONFORMATIONAL DYNAMICS AND THERMODYNAMICS. CHEMICAL REVIEWS 1993, 93(7), 2487
  149527. 502. A REVIEWa
  149528. GABRIEL WEATHERHEAD
  149529. 6747N
  149530. 2/28/96V
  149531. LIPKOWITZ, KENNY B.; PETERSON, MICHAEL A. MOLECULAR MECHANICS IN ORGANIC SYNTHESIS. CHEMICAL REVIEWS 1993, 93(7), 2463
  149532. 86. A REVIEWa
  149533. GABRIEL WEATHERHEAD
  149534. 6748N
  149535. 2/28/96V
  149536. EKSTEROWICZ, JOHN E.; HOUK, K. N. TRANSITION
  149537. STATE MODELING WITH EMPIRICAL FORCE FIELDS. CHEMICAL REVIEWS 1993, 93(7), 2439
  149538.  A REVIEWa
  149539. GABRIEL WEATHERHEAD
  149540. 6749N
  149541. 2/28/96V
  149542. COHEN, N.; BENSON, S. W. ESTIMATION OF HEATS OF FORMATION OF ORGANIC COMPOUNDS BY ADDITIVITY METHODS. CHEMICAL REVIEWS, 1993, 93(7), 2419
  149543. 38. A REVIEW
  149544. GABRIEL WEATHERHEAD
  149545. 6750N
  149546. 2/28/96VzBERRY, R. STEPHEN. POTENTIAL SURFACES AND DYNAMICS: WHAT CLUSTERS TELL US. CHEMICAL REVIEWS 1993, 93(7), 2379
  149547. 94. A REVIEWa
  149548. GABRIEL WEATHERHEAD
  149549. 6751N
  149550. 2/28/96V
  149551. DYKSTRA, CLIFFORD E. ELECTROSTATIC INTERACTION POTENTIALS IN MOLECULAR FORCE FIELDS. CHEMICAL REVIEWS 1993, 93(7), 2339
  149552. 53. A REVIEWa
  149553. GABRIEL WEATHERHEAD
  149554. 6752N
  149555. 2/28/96V{YAMAMOTO, YOSHINORI; ASAO, NAOKI. SELECTIVE REACTIONS USING ALLYLIC METALS. CHEMICAL REVIEWS 1993, 93(6), 2207
  149556. 93. A REVIEWa
  149557. GABRIEL WEATHERHEAD
  149558. 6753N
  149559. 2/28/96V
  149560. KNOCHEL, PAUL; SINGER, ROBERT D. PREPARATION AND REACTIONS OF POLYFUNCTIONAL ORGANOZINC REAGENTS IN ORGANIC SYNTHESIS. CHEMICAL REVIEWS 1993, 93(6), 2117
  149561. 88. A REVIEWa
  149562. GABRIEL WEATHERHEAD
  149563. 6754N
  149564. 2/28/96
  149565. ERIAN, AYMAN WAHBA. THE CHEMISTRY OF BETA
  149566. ENAMINONITRILES AS VERSATILE REAGENTS IN HETEROCYCLIC SYNTHESIS. CHEMICAL REVIEWS 1993,93(6),1991
  149567. 2005. A REVIEWa
  149568. GABRIEL WEATHERHEAD
  149569. 6755N
  149570. 2/28/96VpCORNFORTH, JOHN WARCUP. THE TROUBLE WITH SYNTHESIS. AUSTRALIAN JOURNAL OF CHEMISTRY 1993, 46(2),157
  149571. 70. A REVIEWa
  149572. GABRIEL WEATHERHEAD
  149573. 6756N
  149574. 2/28/96V
  149575. CAMBIE, RICHARD C.; RUTLEDGE, PETER S.; WOODGATE, PAUL D. TRANSFORMATIONS OF PODOCARPIC ACID. AUSTRALIAN JOURNAL OF CHEMISTRY 1993, 46(10), 1447
  149576. 71. A REVIEWa
  149577. GABRIEL WEATHERHEAD
  149578. 6757N
  149579. 2/28/96V
  149580. HUNTER, CHRISTOPHER A. ARENE
  149581. ARENE INTERACTIONS: ELECTROSTATIC OR CHARGE
  149582. TRANSFER? ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(11),1584
  149583. 86. A REVIEWa
  149584. GABRIEL WEATHERHEAD
  149585. 6758N
  149586. 2/28/96
  149587. BLOKZIJL, WILFRIED; ENGBERTS, JAN B. F. N. HYDROPHOBIC EFFECTS: OPINIONS AND FACTS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(11),1545
  149588. 79. A REVIEWa
  149589. GABRIEL WEATHERHEAD
  149590. 6759N
  149591. 2/28/96V
  149592. HERRMANN, WOLFGANG A.; KOHLPAINTNER, CHRISTIAN W. WATER
  149593. SOLUBLE LIGANDS, METAL COMPLEXES, AND COMPLEX CATALYSTS: SYNERGISM OF HOMOGENEOUS AND HETEROGENEOUS CATALYSIS. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(11), 1524
  149594. 44. A REVIEWa
  149595. GABRIEL WEATHERHEAD
  149596. 6760N
  149597. 2/28/96V
  149598. SCHWARZ, HELMUT. THE MECHANISM OF FULLERENE FORMATION. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(10), 1412
  149599. 15. A REVIEWa
  149600. GABRIEL WEATHERHEAD
  149601. 6761N
  149602. 2/28/96V
  149603. KURRECK, HARRY. TRIPLET STATES IN ORGANIC CHEMISTRY. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993,32(10),1409
  149604. 11. A REVIEWa
  149605. GABRIEL WEATHERHEAD
  149606. 6762N
  149607. 2/28/96
  149608. NICOLAOU, K. C. THE BATTLE OF CALICHEAMICIN 1. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993,32(10),5377
  149609. 85. A REVIEWa
  149610. GABRIEL WEATHERHEAD
  149611. 6763N
  149612. 2/28/96V
  149613. LEUMANN, CHRISTIAN. NEW DEVELOPMENTS IN THE CHEMISTRY OF CATALYTIC ANTIBODIES. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(9),1291
  149614. 93. A REVIEWa
  149615. GABRIEL WEATHERHEAD
  149616. 6764N
  149617. 2/28/96V
  149618. GIANNIS, ANTHANASSIOS; KOLTER, THOMAS. PEPTIDO
  149619. MIMETICS FOR RECEPTOR LIGANDS
  149620. DISCOVERY, DEVELOPMENT, AND MEDICAL PERSPECTIVES. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(9),1244
  149621. 67. A REVIEWa
  149622. GABRIEL WEATHERHEAD
  149623. 6765N
  149624. 2/28/96V
  149625. SCOTT, A. I. HOW NATURE SYNTHESIZES VITAMIN B12
  149626. A SURVEY OF THE LAST FOUR BILLION YEARS ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(9), 1223
  149627. 43. A REVIEWa
  149628. GABRIEL WEATHERHEAD
  149629. 6766N
  149630. 2/28/96
  149631. GRIMMETT, M. ROSS. HALOGENATION OF HETEROCYCLES: II. SIX
  149632.  AND SEVEN
  149633. MEMBERED RINGS. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993, 58, 271
  149634. 345. A REVIEWa
  149635. GABRIEL WEATHERHEAD
  149636. 6767N
  149637. 2/28/96V
  149638. HURST, DEREK T. THE NITRATION OF PHENYL
  149639. SUBSTITUTED HETEROCYCLES. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993, 58, 215
  149640. 269. A REVIEWa
  149641. GABRIEL WEATHERHEAD
  149642. 6768N
  149643. 2/28/96V
  149644. COSTERO, ANA M. THE CHEMISTRY OF UNSATURATED NITROGEN
  149645. HETEROCYCLIC COMPOUNDS CONTAINING CARBONYL GROUPS. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993, 58, 171
  149646. 214. A REVIEWa
  149647. GABRIEL WEATHERHEAD
  149648. 6769N
  149649. 2/28/96VnBLACKMAN, ALLAN. REACTIONS OF COORDINATED LIGANDS. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993,58,123
  149650. 70. A REVIEWa
  149651. GABRIEL WEATHERHEAD
  149652. 6770N
  149653. 2/28/96V
  149654. SADEKOV, IGOR D.; MINKIN, VLADIMIR I. TELLURIUM
  149655. CONTAINING HETEROCYCLES WITH TWO HETEROATOMS. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993, 58, 47
  149656. 121. A REVIEWa
  149657. GABRIEL WEATHERHEAD
  149658. 6771N
  149659. 2/28/96V
  149660. ESKER, JOHN L.; NEWCOMB, MARTIN. THE GENERATION OF NITROGEN RADICALS AND THEIR CYCLIZATIONS FOR THE CONSTRUCTION OF THE PYRROLIDINE NUCLEUS. ADVANCES IN HETEROCYCLIC CHEMISTRY 1993, 58,1
  149661. 45. A REVIEWa
  149662. GABRIEL WEATHERHEAD
  149663. 6772N
  149664. 2/28/96V
  149665. DELAUDE, LIONEL; LASZLO, PIERRE; SMITH, KEITH. HEIGHTENED SELECTIVITY IN AROMATIC NITRATIONS AND CHLORINATIONS BY THE USE OF SOLID SUPPORTS AND CATALYSTS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(12),607
  149666. 13. A REVIEWa
  149667. GABRIEL WEATHERHEAD
  149668. 6773N
  149669. 2/28/96V
  149670. CRAMER, CHRISTOPHER J.; FAMINI, GEORGE R.; LOWREY, ALFRED H. USE OF CALCULATED QUANTUM CHEMICAL PROPERTIES AS SURROGATES FOR SOLVATOCHROMIC PARAMETERS IN STRUCTURE
  149671. ACTIVITY RELATIONSHIPS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(11), 599
  149672. 605. A REVIEWa
  149673. GABRIEL WEATHERHEAD
  149674. 6774N
  149675. 2/28/96
  149676. RIGBY, JAMES H. TRANSITION METAL PROMOTED HIGHER
  149677. ORDER CYCLOADDITION REACTIONS IN ORGANIC SYNTHESIS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(11),579
  149678. 85. A REVIEWa
  149679. GABRIEL WEATHERHEAD
  149680. 6775N
  149681. 2/28/96V
  149682. KUTNEY, JAMES P. PLANT CELL CULTURE COMBINED WITH CHEMISTRY: A POWERFUL ROUTE TO COMPLEX NATURAL PRODUCTS. ACCOUNTS OF CHEMICAL RESEARCH 1993,26(10),559
  149683. 66. A REVIEWa
  149684. GABRIEL WEATHERHEAD
  149685. 6776N
  149686. 2/28/96V
  149687. HILVERT, DONALD. ANTIBODY CATALYSIS OF CARBON
  149688. CARBON BOND FORMATION AND CLEAVAGE. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(10), 552
  149689. 58. A REVIEWa
  149690. GABRIEL WEATHERHEAD
  149691. HOUBEN
  149692. WEYLC
  149693. HANACK; BOOK, REVIEW, CARBANION, ORGANOMETALLIC, ACYL ANION, ALKENYL, ALPHA AMINO, ALPHA ALKOXY, TIN LITHIUM EXCHANGE, SELENIUM, SULFUR, TIN, HALOGEN.M
  149694. 6777N
  149695. 2/28/96V+CARBANIONEN
  149696. METHODEN DER ORGANISCHEN CHEMIEW
  149697. 1993  E19Da
  149698. GABRIEL WEATHERHEAD
  149699. THEBTARARONTH; BOOK, REVIEW, CATIONIC, RADICAL, ANIONIC, METAL
  149700. CATALYZED CYCLIZATIONS, IMINIUM IONS, OXONIUM, SUBSTITUTION, CONJUGATE ADDITIONM
  149701. 6778N
  149702. 2/28/96V
  149703. CYCLIZATION REACTIONSW
  149704. 1994a
  149705. GABRIEL WEATHERHEAD
  149706. ORG. PREP. PROC. INT.C^OH; DIELS
  149707. ALDER, ASYMMETRIC, REVIEW, CATALYSIS, HETERO, IMINE, ALDEHYDE, DIENE, INTRAMOLECULARM
  149708. 6779N
  149709. 2/28/96V?REAGENT
  149710. CONTROLLED ASYMMETRIC DIELS
  149711. ALDER REACTIONS.  A REVIEW.W
  149712. 1994  26  129
  149713. GABRIEL WEATHERHEAD
  149714. ORG. PREP. PROC. INT.C
  149715. HUTCHINS; IMINE, AMINE, IMINIUM, HYDRAZONE, KETOXIME, PHOSPHINYL IMINES, SULFINAMIDES, SULFONYLIMINES, REDUCTION, REVIEW, PYRROLINEM
  149716. 6780N
  149717. 2/28/96VAASYMMETRIC REDUCTIONS OF CARBON
  149718. NITROGEN DOUBLE BONDS.  A REVIEW.W
  149719. 1994  26  193
  149720. GABRIEL WEATHERHEAD
  149721. TETRAHEDRONC#DUTHALER, R.O.; AMINO ACIDS, REVIEWM
  149722. 6781N
  149723. 2/28/96VIRECENT DEVELOPMENTS IN THE STEREOSELECTIVE SYNTHESIS OF ALPHA AMINO ACIDSW
  149724. 1994  50  1539
  149725. 1650a
  149726. GABRIEL WEATHERHEAD
  149727. CHEM. SOC. REV.CGNONHEBEL, D.C.; RADICAL, CYCLOPROPYLMETHYL, CYCLOPROPYLCARBINYL, REVIEWM
  149728. 6782N
  149729. 2/28/96V7THE CHEMISTRY OF CYCLOPROPYLMETHYL AND RELATED RADICALSW
  149730. 1993  23  347a
  149731. GABRIEL WEATHERHEAD
  149732. NAT. PROD. REPORTSC}MICHAEL, J.P.; REVIEW, INDOLIZIDINE, QUINOLIZIDINE, SLAFRAMINE, CASTANOSPERMINE, SWAINSONINE, ANALOGS, MONOMORINE, PICLAVINESM
  149733. 6783N
  149734. 2/28/96V(INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDSW
  149735. 1994  1  17
  149736. GABRIEL WEATHERHEAD
  149737. RECUIEL TRAV. CHIM.CjLISKAMP, R.M.J.; PEPTIDE, AMINO ACID, REVIEW, CONFORMATIONALLY RESTRICTED, INDOLIZIDINE, N
  149738. ACYLIMINIUM IONM
  149739. 6784N
  149740. 2/28/96VnCONFORMATIONALLY RESTRICTED AMINO ACIDS AND DIPEPTIDES, (NON) PEPTIDOMIMETICS AND SECONDARY STRUCTURE MIMETICSW
  149741. 1994  113  1
  149742. GABRIEL WEATHERHEAD
  149743. BOOKC7LOUNASMAA, M.; TAMMINEN, T.;  TROPANE ALKALOIDS, REVIEWM
  149744. 6785N
  149745. 2/28/96V)THE TROPANE ALKALOIDS, IN "THE ALKALOIDS"W
  149746. 1993  44  1
  149747. GABRIEL WEATHERHEAD
  149748. C1THATCHER, G. R. J.; BOOK, ANOMERIC EFFECT, REVIEWM
  149749. 6786N
  149750. 2/28/96V;THE ANOMERIC EFFECT AND ASSOCIATED STEREOELECTRONIC EFFECTSW
  149751. 1993a
  149752. GABRIEL WEATHERHEAD
  149753. JOCCRERKER; IMINE, ENAMINE, TAUTOMERIC EQUILIBRIUM, ISONITRILE, ZIRCONIUM DIENE COMPLEXM
  149754. 6787N
  149755. 2/28/96V9FORMATION OF STABLE, ISOLABLE CONJUGATED PRIMARY ENAMINESW
  149756. 1993  58  6771
  149757. 6778a
  149758. GABRIEL WEATHERHEAD
  149759. SYNLETTC
  149760. SMADJA, W.; RADICAL, STEREOCENTER, ASYMETRIC, DIASTEREOFACIAL CONTROL, REVIEW, CRAM, FELKIN, FLEMING, HOUK MODELS, ALPHA AMINO RADICALSM
  149761. 6788N
  149762. 2/28/96VEACYCLIC DIASTEREOFACIAL SELECTION IN INTERMOLECULAR RADICAL REACTIONSW
  149763. 1994  1
  149764. GABRIEL WEATHERHEAD
  149765. NAT. PROD. REPORTSC=MICHAEL, J. P.; INDOLIZIDINE, QUINOLIZIDINE, ALKALOID, REVIEWM
  149766. 6789N
  149767. 2/28/96V(INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDSW
  149768. 1993  10  51
  149769. GABRIEL WEATHERHEAD
  149770. J. HET. CHEM.C&SPECKAMP; REVIEW, RADICAL, IMINIUM IONM
  149771. 6790N
  149772. 2/28/96
  149773. VMNEW ASPECTS OF OLD REACTIONS.  CATIONS AND RADICALS IN HETEROCYCLIC CHEMISTRYW
  149774. 1992  29  653
  149775. GABRIEL WEATHERHEAD
  149776. ANG. CHEM., INT. ED. ENGL.CHREISER, O.; PI ALLYL PALLADIUM, ASYMMETRIC, REVIEW, ALLYLIC SUBSTITUTIONM
  149777. 6791N
  149778. 2/28/96V:PALLADIUM CATALYZED, ENANTIOSELECTIVE ALLYLIC SUBSTITUTIONW
  149779. 1993  32  547
  149780. GABRIEL WEATHERHEAD
  149781. ACTA CHEM. SCAND.CBMARTIN, A. R.; YANG, Y.; REVIEW, SUZUKI COUPLING, CROSS, PALLADIUMM
  149782. 6792N
  149783. 2/28/96V^PALLADIUM CATALYZED CROSS COUPLING REACTIONS OF ORGANOBORONIC ACIDS WITH ORGANIC ELECTROPHILESW
  149784. 1993  47  221
  149785. GABRIEL WEATHERHEAD
  149786. ACCTS. CHEM. RES.C;WONG; AZA SUGAR, ENZYME, GLYCOPROCESSING INHIBITORS, REVIEWM
  149787. 6793N
  149788. 2/28/96V{ENZYME
  149789. CATALYZED ORGANIC SYNTHESIS:  PRACTICAL ROUTES TO AZA SUGARS AND THEIR ANALOGS FOR USE AS GLYCOPROCESSING INHIBITORSW
  149790. 1993  26  182
  149791. GABRIEL WEATHERHEAD
  149792. TETRAHEDRONC,BACKVALL; REVIEW, ORGANOPALLADIUM, PALLADIUMM
  149793. 2/28/96V=PALLADIUM IN ORGANIC SYNTHESIS
  149794. TETRAHEDRON SYMPOSIUM IN PRINTW
  149795. 1994  50  ISSUE #10a
  149796. GABRIEL WEATHERHEAD
  149797. ADV. HET. CHEM.C
  149798. ESKER; J. L.; NEWCOMB, M.; RADICAL, N
  149799. CENTERED, AMINYL, AMIDYL, PYRROLIDINE, CHLORAMINE, SULFENAMIDE, AMINIUM CATION RADICALS, ADDITION TO ALKENES, REVIEW, TETRAZENESM
  149800. 6795N
  149801. 2/28/96VjTHE GENERATION OF NITROGEN RADICALS AND THEIR CYCLIZATIONS FOR THE CONSTRUCTION OF THE PYRROLIDINE NUCLEUSW
  149802. 1993  58  1
  149803. GABRIEL WEATHERHEAD
  149804. ACC CHEM RESCOADAM EPOXIDE EPOXIDATION SINGLET OXYGEN REVIEW SHARPLESS ALKENE TITANIUM CHIRALM
  149805. 6796N
  149806. 2/28/96V5METAL CATALYZED DIRECT HYDROXY EPOXIDATION OF OLEFINSW
  149807. VOL 27 1994 P 57a
  149808. GABRIEL WEATHERHEAD
  149809. ORG PREP PROCEDURE INTC    HUGHES DLM
  149810. 6797N
  149811. 2/28/96V2PROGRESS IN THE FISCHER INDOLE REACTION 
  149812.  A REVIEWW
  149813. 1993 DECX
  149814. 25(6)a
  149815. GABRIEL WEATHERHEAD
  149816. ORG PREP PROCEDURE INTC    NATALE NRM
  149817. 6798N
  149818. 2/28/96
  149819. V/THE LATERAL METALATION OF ISOXAZOLES 
  149820.  A REVIEWW
  149821. 1993 OCTX
  149822. 25(5)a
  149823. GABRIEL WEATHERHEAD
  149824. ORG PREP PROCEDURE INTC
  149825. KARP GMM
  149826. 6799N
  149827. 2/28/96V:PREPARATION AND REACTIONS OF INDOLIN
  149828. 2(3H)
  149829. ONES 
  149830.  A REVIEWW
  149831. 1993 OCTX
  149832. 25(5)a
  149833. GABRIEL WEATHERHEAD
  149834. 6800N
  149835. 2/28/96V
  149836. KANEMATSU, KEN. MOLECULAR DESIGN AND SYNTHESES OF BIOLOGICALLY ACTIVE COMPOUNDS VIA INTRAMOLECULAR ALLENE CYCLOADDITION REACTION STRATEGY. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149837. GABRIEL WEATHERHEAD
  149838. 6801N
  149839. 2/28/96V
  149840. TROFIMOV, BORIS A.; NEDOLYA, NINA A. A NEW STRATEGY IN THE SYNTHESIS OF EPOXY RESINS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149841. GABRIEL WEATHERHEAD
  149842. 6802N
  149843. 2/28/96
  149844. KUMADAKI, ITSUMARO. STERIC EFFECT OF A TRIFLUO ROMETHYL GROUP BASED ON THE RESULTS OF ENE REACTION OF TRIFLUOROMETHYL CARBONYL COMPOUNDS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149845. GABRIEL WEATHERHEAD
  149846. 6803N
  149847. 2/28/96V
  149848. SHIMIZU, NOBUJIRO. SILICON EFFECTS IN SOLVOLYSIS AND RELATED REACTIONS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149849. GABRIEL WEATHERHEAD
  149850. 6804N
  149851. 2/28/96V
  149852. NEGORO, TAKESHI; OAE, SHIGERU. LIGAND COUPLING WITH HYPERVALENT SPECIES II. ON COPPER ATOM. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149853. GABRIEL WEATHERHEAD
  149854. 6805N
  149855. 2/28/96V
  149856. NITTA, MAKOTO. REACTIONS OF (VINYLIMINO)PHOSPHORANES AND RELATED COMPOUNDS. NOVEL SYNTHESIS OF NITROGEN HETEROCYCLES. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149857. GABRIEL WEATHERHEAD
  149858. 6806N
  149859. 2/28/96V
  149860. COMASSETO,JOAOV. VINYLICTELLURIDES: PRECURSORS OF VINYLLITHIUM AND VINYLCOPPER REAGENTS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149861. GABRIEL WEATHERHEAD
  149862. 6807N
  149863. 2/28/96V
  149864. WLADISLAW, BLANKA; MARZORATI, LILIANA. REACTIONS OF SULFINYL AND SULFONYL CARBANIONS WITH SULFENYLATING AGENTS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149865. GABRIEL WEATHERHEAD
  149866. 6808N
  149867. 2/28/96V
  149868. MARKOVSKY, LEONID N.; PENKOVSKY, VLADIMIR V.; SHERMOLOVICH, YURI G. THIONITROSO COMPOUNDS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149869. GABRIEL WEATHERHEAD
  149870. 6809N
  149871. 2/28/96V
  149872. FREEMAN, FILLMORE; AREGULLIN, MANUEL; RODRIGUEZ, ELOY. NATURALLY OCCURRING 1,2
  149873. DITHIINS. REVIEWS ON HETEROATOM CHEMISTRY, VOLUME 9.  SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1993.a
  149874. GABRIEL WEATHERHEAD
  149875. 6810N
  149876. 2/28/96V
  149877. KUK'HAR, V. P.; SVISTUNOVA, N. YU.; SOLODENKO, V. A.; SOLOSHONOK, V. A. ASYMMETRIC SYNTHESIS OF FLUORINE AND PHOSPHORUS
  149878. CONTAINING ANALOGUES OF AMINOACIDS. RUSSIAN CHEMICAL REVIEWS 1993, 62(3), 261.a
  149879. GABRIEL WEATHERHEAD
  149880. 6811N
  149881. 2/28/96V
  149882. FURIN,G.G. PHOSPHORUS
  149883. CONTAININGNUCLEOPHILES IN REACTIONS WITH POLYFLUORINATED ORGANIC COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1993, 62(3), 243.a
  149884. GABRIEL WEATHERHEAD
  149885. 6812N
  149886. 2/28/96V
  149887. KARAKHANOV, R. A.; KELAREV, V. I.; POLIVIN, YU. N. THE SYNTHESIS AND PROPERTIES OF UNSATURATED NITRO COMPOUNDS OF THE FURAN SERIES. RUSSIAN CHEMICAL REVIEWS 1993, 62(2),169.a
  149888. GABRIEL WEATHERHEAD
  149889. 6813N
  149890. 2/28/96V
  149891. ZLOTIN, S. G.; LUK'YANOV, O. A. REGIOSELECTIVE METHODS OF SYNTHESIS OF ASYMMETRICALLY SUBSTITUTED DIAZENE OXIDES. RUSSIAN CHEMICAL REVIEWS 1993, 62(2), 143.a
  149892. GABRIEL WEATHERHEAD
  149893. 6814N
  149894. 2/28/96
  149895. KNORRE, D. G.; FEDOROVA, O. S.; FROLOVA, E. I. OXIDATIVE DEGRADATION OF NUCLEIC ACIDS. RUSSIAN CHEMICAL REVIEWS 1993, 62(1), 65.a
  149896. GABRIEL WEATHERHEAD
  149897. 6815N
  149898. 2/28/96V
  149899. TOPUZYAN, V. O.; NESUNTS, N. S. REACTIONS OF 4,5
  149900.  DIHYDRO
  149901. OXAZOLES WITH OXYGEN
  149902. CONTAINING NUCLEOPHILES. RUSSIAN CHEMICAL REVIEWS 1993, 62(1), 51.a
  149903. GABRIEL WEATHERHEAD
  149904. 6816N
  149905. 2/28/96V
  149906. NABIVACH, V. M.; DMITRIKOV, V. P. THE USE OF CORRELATION EQUATIONS FOR THE PREDICTION OF RETENTION PARAMETERS IN GAS
  149907. LIQUID CHROMATOGRAPHY. RUSSIAN CHEMICAL REVIEWS 1993, 62(1), 23.a
  149908. GABRIEL WEATHERHEAD
  149909. 6817N
  149910. 2/28/96V
  149911. WILLIAMS, IANH. INTERPLAY OF THEORY AND EXPERIMENT IN THE DETERMINATION OF TRANSITION
  149912. STATE STRUCTURE. CHEMICAL SOCIETY REVIEWS 1993, 22(4),277
  149913. GABRIEL WEATHERHEAD
  149914. 6818N
  149915. 2/28/96
  149916. DAVIS, ANTHONY P. CHOLAPHANES ET AL.; STEROIDS AS STRUCTURAL COMPONENTS IN MOLECULAR ENGINEERING. CHEMICAL SOCIETY REVIEWS 1993, 22(4),243
  149917. GABRIEL WEATHERHEAD
  149918. 6819N
  149919. 2/28/96V
  149920. STEWART, JON D.; BENKOVIC, STEPHEN J. CATALYTIC ANTIBODIES: MECHANISTIC AND PRACTICAL CONSIDERATIONS. CHEMICAL SOCIETY REVIEWS 1993, 22(4),213
  149921. GABRIEL WEATHERHEAD
  149922. 6820N
  149923. 2/28/96V
  149924. MCGREGOR, WILLIAM M.; SHERRINGTON, DAVID C. SOME RECENT SYNTHETIC ROUTES TO THIOKETONES AND THIOALDEHYDES. CHEMICAL SOCIETY REVIEWS 1993,22(3),199
  149925. 204.a
  149926. GABRIEL WEATHERHEAD
  149927. 6821N
  149928. 2/28/96V
  149929. LOWN, J. WILLIAM. DISCOVERY AND DEVELOPMENT OF ANTHRACYCLINE ANTITUMOUR ANTIBIOTICS. CHEMICAL SOCIETY REVIEWS 1993, 22(3),165
  149930.  76.a
  149931. GABRIEL WEATHERHEAD
  149932. 6822N
  149933. 2/28/96V
  149934. LEGON, A. C. THE NATURE OF AMMONIUM AND METHYLAMMONIUM HALIDES IN THE VAPOR PHASE: HYDROGEN BONDING VERSUS PROTON TRANSFER. CHEMICAL SOCIETY REVIEWS 1993, 22(3),153FF3.
  149935. GABRIEL WEATHERHEAD
  149936. 6823N
  149937. 2/28/96VwBECKWITH, ATHELSTAN L. J. THE PURSUIT OF SELECTIVITY IN RADICAL REACTIONS. CHEMICAL SOCIETY REVIEWS 1993, 22(3),143
  149938. GABRIEL WEATHERHEAD
  149939. 6824N
  149940. 2/28/96V
  149941. BARRON, ANDREW R. REACTIONS OF GROUP 13 ALKYLS WITH DIOXYGEN AND ELEMENTAL CHALCOGENS: FROM CARELESSNESS TO CHEMISTRY. CHEMICAL SOCIETY REVIEWS 1993, 22(2), 93
  149942. GABRIEL WEATHERHEAD
  149943. 6825N
  149944. 2/28/96VKCAUBERE, PAUL. UNIMETAL SUPER BASES. CHEMICAL REVIEWS 1993, 93(6), 2317
  149945. GABRIEL WEATHERHEAD
  149946. 6826N
  149947. 2/28/96V
  149948. ABE, IKURO; ROHMER, MICHEL; PRESTWICH, GLENN D. ENZYMATIC CYCLIZATION OF SQUALENE AND OXIDOSQUALENE TO STEROLS AND TRITERPENES. CHEMICAL REVIEWS 1993, 93(6), 2189
  149949. 206.a
  149950. GABRIEL WEATHERHEAD
  149951. 6827N
  149952. 2/28/96V~DOWD, PAUL; ZHANG, WEI. FREE RADICAL
  149953. MEDIATED RING EXPANSION AND RELATED ANNULATIONS. CHEMICAL REVIEWS 1993, 93(6), 2091
  149954.  115.a
  149955. GABRIEL WEATHERHEAD
  149956. 6828N
  149957. 2/28/96VKNEWKOME, GEORGE R. PYRIDYLPHOSPHINES. CHEMICAL REVIEWS 1993, 93(6),2067
  149958. GABRIEL WEATHERHEAD
  149959. 6829N
  149960. 2/28/96VeFUJI, KAORU. ASYMMETRIC CREATION OF QUATERNARY CARBON CENTERS. CHEMICAL REVIEWS 1993, 93(6), 2037FF6.a
  149961. GABRIEL WEATHERHEAD
  149962. 6830N
  149963. 2/28/96V
  149964. LI, CHAO JUN. ORGANIC REACTIONS IN AQUEOUS MEDIA
  149965. WITH A FOCUS ON CARBON
  149966. CARBON BOND FORMATION. CHEMICAL REVIEWS 1993, 93(6),2023
  149967. GABRIEL WEATHERHEAD
  149968. 6831N
  149969. 2/28/96V
  149970. MYERS, RICHARD A.; CRUZ, LOURDES J.; RIVIER, JEAN E.; OLIVERA, BALDOMERO M. CONUS PEPTIDES AS CHEMICAL PROBES FOR RECEPTORS AND ION CHANNELS. CHEMICAL REVIEWS 1923, 93(5),1923
  149971.  36.a
  149972. GABRIEL WEATHERHEAD
  149973. 6832N
  149974. 2/28/96V
  149975. MOLINSKI, TADEUSZ F. MARINE PYRIDOACRIDINE ALKALOIDS: STRUCTURE, SYNTHESIS, AND BIOLOGICAL CHEMISTRY. CHEMICAL REVIEWS 1993,93(5),1825
  149976. GABRIEL WEATHERHEAD
  149977. WILEY
  149978. 5CRJOHNSON; YLIDE, WITTIG, AZA
  149979. WITTIG, IMINO PHOSPHORANE, ALKENE, IMINE, REVIEW, BOOKM
  149980. 6833N
  149981. 2/28/96V
  149982. YLIDES AND IMINES OF PHOSPHORUSW
  149983. 1993a
  149984. GABRIEL WEATHERHEAD
  149985. WILEYC,HO; REVIEW, BOOK, HETEROCYCLIC FRAGMENTATIONM
  149986. 6834N
  149987. 2/28/96V/HETEROCYCLIC FRAGMENTATION OF ORGANIC MOLECULESW
  149988. 1993a
  149989. GABRIEL WEATHERHEAD
  149990. WILEYCILEFFLER; BOOK, REVIEW, RADICAL, ELECTRON TRANSFER, SYNTHETIC APPLICATIONSM
  149991. 6835N
  149992. 2/28/96V AN INTRODUCTION TO FREE RADICALSW
  149993. 1993a
  149994. GABRIEL WEATHERHEAD
  149995. WILEYC.MORRISON; PHOTOCHEMICAL SWITCHES, BOOK, REVIEWM
  149996. 6836N
  149997. 2/28/96V-BIOLOGICAL APPLICATIONS OF MOLECULAR SWITCHESW
  149998. 1993 2a
  149999. GABRIEL WEATHERHEAD
  150000. WILEYCwKOSKINEN; BOOK, REVIEW, ASYMMETRIC SYNTHESIS, CARBOHYDRATES, AMINO ACIDS, PEPTIDES, NUCLEOSIDES, ISOPRENOIDS, ALKALOIDSM
  150001. 6837N
  150002. 2/28/96V(ASYMMETRIC SYNTHESIS OF NATURAL PRODUCTSW
  150003. 1993a
  150004. GABRIEL WEATHERHEAD
  150005. J. WILEY
  150006. :CSELIEL, WILEN; STEREOCHEMISTRY, SYMMETRY, RESOLUTION CONFORMATIONAL ANALYSIS, REVIEWM
  150007. 6838N
  150008. 2/28/96V$STEREOCHEMISTRY OF ORGANIC COMPOUNDSW
  150009. 1994a
  150010. GABRIEL WEATHERHEAD
  150011. FALCK; BIS SULFONE, ALCOHOL, MITSUNOBU, CYCLOPENTANE, CYCLOBUTANE, CYCLOPROPANE, CYCLOHEXANE FORMATION, REVIEW OF BIS SULFONE TRANSFORMATIONS, INCLUDING REDUCTION, REDUCTIVE ALKYLATION, JULIA COUPLING, CONVERSION TO KETONEM
  150012. 6839N
  150013. 2/28/96V5STEREOSPECIFIC DEHYDRATIVE ALKYLATION OF BIS SULFONESW
  150014. 1993 58 5892
  150015. 5894a
  150016. GABRIEL WEATHERHEAD
  150017. ADV. THEOR. INT. MOL.CFLEASE AND SHEA; REVIEW, STRAINED ALKENE, AMIDE, BRIDGEHEAD, ANTI BREDTM
  150018. 6840N
  150019. 2/28/96VXA COMPILATION AND ANALYSIS OF STRUCTURAL DATA OF DISTORTED BRIDGEHEAD OLEFINS AND AMIDESW
  150020. 1992 2a
  150021. GABRIEL WEATHERHEAD
  150022. TOP. CURR. CHEM.C"ADAM; DIOXIRANE, OXIDATION, REVIEWM
  150023. 6841N
  150024. 2/28/96V*DIOXIRANES:  OXIDATION CHEMISTRY MADE EASYW
  150025. 1993 164 45
  150026. GABRIEL WEATHERHEAD
  150027. TETRAHEDRON: ASYMM.
  150028. >CMWALLBAUM; OXAZABOROLIDINE, REVIEW, CHIRAL, REDUCTION, CYCLOADDITION, ADDITIONM
  150029. 6842N
  150030. 2/28/96V1ASYMMETRIC SYNTHESIS WITH CHIRAL OXAZABOROLIDINESW
  150031. 1992 3 1475
  150032. 1504a
  150033. GABRIEL WEATHERHEAD
  150034. ?B    SYNTHESISCdLOHRAY; REVIEW, CYCLIC SULFATES, SULFITES, ALKYLATION, SN2, EPOXIDE LIKE, DISPLACEMENT, SUBSTITUTIONM
  150035. 6843N
  150036. 2/28/96V;CYCLIC SULFITES AND CYCLIC SULFATES:  EPOXIDE LIKE SYNTHONSW
  150037. 1992  1035
  150038. 1052a
  150039. GABRIEL WEATHERHEAD
  150040. RUSS. CHEM. REV.C SIMONOVA; NITRENIUM IONS, REVIEWM
  150041. 6844N
  150042. 2/28/96V1CURRENT APPROACH TO THE PROBLEM OF NITRENIUM IONSW
  150043. 1992 61 584a
  150044. GABRIEL WEATHERHEAD
  150045. ORG. REACT.C+RABIDEAU; BIRCH REDUCTION, AROMATIC, REVIEWM
  150046. 6845N
  150047. 2/28/96V)THE BIRCH REDUCTION OF AROMATIC COMPOUNDSW
  150048. 1992 42 1
  150049. GABRIEL WEATHERHEAD
  150050. ORG. PREP. PROC. INT.CXSIBI, M.; REVIEW, N
  150051. METHOXY
  150052. METHYLAMIDES, ACYLATION, CARBANION, KETONE, AMIDE, WEINREBM
  150053. 6846N
  150054. 2/28/96
  150055. BVACHEMISTRY OF N
  150056. METHOXY
  150057. METHYLAMIDES.  APPLICATIONS IN SYNTHESISW
  150058. 1993 25 15
  150059. GABRIEL WEATHERHEAD
  150060. SYNLETTC
  150061. BLACK; REVIEW, INDOLE, ELECTROPHILIC SUBSTITUTION, 2,2'
  150062. BIINDOLES, NITRONE CYCLOADDITIONS, HECK REACTION, PALLADIUM OXIDATIVE COUPLINGM
  150063. 6847N
  150064. 2/28/96V"NEW DIMENSIONS IN INDOLE CHEMISTRYW
  150065. 1993  246
  150066. GABRIEL WEATHERHEAD
  150067. SYNLETTC
  150068. JURCZAK; AMINO HYDROXY ACIDS, CARBOHYDRATE SERINE, THREONINE, CHIRON, CHIRAL POOL, 4+2 CYCLOADDITION, PYRAN, ALDEHYDE, CYCLOCONDENSATION, REVIEWM
  150069. 6848N
  150070. 2/28/96VEALPHA AMINO BETA HYDROXY ACIDS IN THE TOTAL SYNTHESIS OF AMINO SUGARSW
  150071. 1993  241
  150072. GABRIEL WEATHERHEAD
  150073. BOOKCMMCQUILLIN, PARKER, STEPHENSON; BOOK, TRANSITION METAL ORGANOMETALLICS, REVIEWM
  150074. 6849N
  150075. 2/28/96V6TRANSITION METAL ORGANOMETALLICS FOR ORGANIC SYNTHESISW
  150076. 1991a
  150077. GABRIEL WEATHERHEAD
  150078. ADV. CYCLOADDITIONCPKANEMASA; REVIEW, AZOMETHINE YLIDE, 2
  150079. AZAALLYL ANION, CYCLOADDITION, PYRROLIDINEM
  150080. 2/28/96V
  150081. METALATED AZOMETHINE YLIDESW
  150082. 1993 3a
  150083. GABRIEL WEATHERHEAD
  150084. ADV. CYCLOADDITIONC8BUNNELLE; OZONOLYSIS, CARBONYL OXIDE, TRIOXOLANE, REVIEWM
  150085. 6852N
  150086. 2/28/96VPSUBSTITUENT AND STRUCTURAL EFFECTS IN THE OZONOLYSIS OF CYCLIC VINYLOGOUS ESTERSW
  150087. 1993 3a
  150088. GABRIEL WEATHERHEAD
  150089. IB    SYNTHESISCAMITCHELL; REVIEW, STILLE COUPLING, ORGANOSTANNANE, TIN, PALLADIUMM
  150090. 6853N
  150091. 2/28/96V4PALLADIUM CATALYZED REACTIONS OF ORGANOTIN COMPOUNDSW
  150092. 1992  803
  150093. GABRIEL WEATHERHEAD
  150094. ADV. CARBANION CHEM.C/HUA; SULFINYL ANIONS, IMINES, ALKALOIDS, REVIEWM
  150095. 6854N
  150096. 2/28/96V7CHIRAL SULFINYLALLYL AND ALPHA SULFINYL KETIMINE ANIONSW
  150097. 1992 1a
  150098. GABRIEL WEATHERHEAD
  150099. ADV. CARBANION CHEM.CHBRAUN; SNIECKUS, ED.; CARBANION, ENOLATE, ALDOL, STEREOSELECTIVE, REVIEWM
  150100. 6855N
  150101. 2/28/96V6RECENT DEVELOPMENTS IN STEREOSELECTIVE ALDOL REACTIONSW
  150102. 1992 1a
  150103. GABRIEL WEATHERHEAD
  150104. SYNLETTC&KNOELKER; ORGANOIRON, ALKALOID, REVIEWM
  150105. 2/28/96V[IRON
  150106. MEDIATED SYNTHESIS OF HETEROCYCLIC RING SYSTEMS AND APPLICATIONS IN ALKALOID CHEMISTRYW
  150107. 1992  371
  150108. GABRIEL WEATHERHEAD
  150109. NATURAL PROD. REPORTSC'ROBINS; PYRROLIZIDINE ALKALOIDS, REVIEWM
  150110. 6857N
  150111. 2/28/96V
  150112. PYRROLIZIDINE ALKALOIDSW
  150113. 1992 9 313
  150114. GABRIEL WEATHERHEAD
  150115. CHEM. REV.CGKAGAN; DIELS ALDER, CYCLOADDITION, CHIRAL, CATALYTIC ASYMMETRIC, REVIEWM
  150116. 6858N
  150117. 2/28/96V*CATALYTIC ASYMMETRIC DIELS
  150118. ALDER REACTIONSW
  150119. 1992 92 1007
  150120. 1009a
  150121. GABRIEL WEATHERHEAD
  150122. CHEM. REV.C+WHITESELL; CHIRAL AUXILIARY, LIGAND, REVIEWM
  150123. 6859N
  150124. 2/28/96V#CYCLOHEXYL
  150125. BASED CHIRAL AUXILIARIESW
  150126. 1992 92 953
  150127. GABRIEL WEATHERHEAD
  150128. CHEM. REV.C7DAVIS; OXAZIRIDINE, OXIDATION, ENOLATE, ALCOHOL, REVIEWM
  150129. 6860N
  150130. 2/28/96V@ASYMMETRIC HYDROXYLATION OF ENOLATES WITH N
  150131. SULFONYLOXAZIRIDINESW
  150132. 1992 92 919
  150133. GABRIEL WEATHERHEAD
  150134. CHEM. REV.C8WILLIAMS; ASYMMETRIC ALKYLATION, GLYCINE ENOLATE, REVIEWM
  150135. 2/28/96V$ASYMMETRIC SYNTHESIS OF ARYLGLYCINESW
  150136. 1992 92 889
  150137. GABRIEL WEATHERHEAD
  150138. CHEM. REV.C1SCHURIG; OXIRANE, EPOXIDE, ALKENE, CHIRAL, REVIEWM
  150139. 6862N
  150140. 2/28/96VpMETAL
  150141. MEDIATED ENANTIOSELECTIVE ACCESS TO UNFUNCTIONALIZED ALIPHATIC OXIRANES:  PROCHIRAL AND CHIRAL RECOGNITIONW
  150142. 1992 92 873
  150143. GABRIEL WEATHERHEAD
  150144. CHEM. REV.CIROSSITER; CONJUGATE ADDITION, ASYMMETRIC, REVIEW, CHIRAL LIGANDS, CUPRATEM
  150145. 6863N
  150146. 2/28/96V
  150147. ASYMMETRIC CONJUGATE ADDITIONW
  150148. 1992 92 771
  150149. GABRIEL WEATHERHEAD
  150150. ANGEW. CHEM., INT. ED. ENGL.CHPATERSON; EPOXIDE, MESO, CHIRAL LEWIS ACID, NUCLEOPHILIC OPENING, REVIEWM
  150151. 6864N
  150152. 2/28/96VrMESO
  150153. EPOXIDES IN ASYMMETRIC SYNTHESIS:  ENANTIOSELECTIVE OPENING BY NUCLEOPHILES IN PRESENCE OF CHIRAL LEWIS ACIDSW
  150154. 1992 31 1179
  150155. 1180a
  150156. GABRIEL WEATHERHEAD
  150157. ANGEW. CHEM., INT. ED. ENGL.CBLOHRAY; OXAZABOROLIDINE, CATALYSIS, REDUCTION, DIELS
  150158. ALDER, REVIEWM
  150159. 6865N
  150160. 2/28/96
  150161. UVDOXAZABOROLIDINES AND DIOXABOROLIDINES IN ENANTIOSELECTIVE CATALYSIS.W
  150162. 1992 31 729
  150163. GABRIEL WEATHERHEAD
  150164. ALDRICHIMICA ACTACGWILLIAMS; ALPHA AMINO ACIDS, CHIRAL ENOLATE, GLYCINE, OXAZINONE, REVIEWM
  150165. 6866N
  150166. 2/28/96V)ASYMMETRIC SYNTHESES OF ALPHA AMINO ACIDSW
  150167. 1992 24 11
  150168. 13, 15
  150169. GABRIEL WEATHERHEAD
  150170. ACCTS. CHEM. RES.C5COLLUM; TMEDA, DIAMINE, ORGANOLITHIUM, LIGAND, REVIEWM
  150171. 6867N
  150172. 2/28/96VBIS N,N,N',N'
  150173. TETRAMETHYLETHYLENEDIAMINE A GOOD LIGAND FOR LITHIUM?W
  150174. 1992 25 448
  150175. GABRIEL WEATHERHEAD
  150176. ACCTS. CHEM. RES.C&OVERMAN; CATIONIC CYCLIZATIONS, REVIEWM
  150177. 6868N
  150178. 2/28/96V2CHARGE IN REACTION DESIGN.  CATIONIC CYCLIZATIONS.W
  150179. 1992 25 352
  150180. GABRIEL WEATHERHEAD
  150181. J. CHEM. SOC., PERKIN TRANS. IIC"FORD, G.; REVIEW ON NITRENIUM IONSM
  150182. 6869N
  150183. 2/28/96V
  150184. NITRENIUM IONSW    1991  607a
  150185. GABRIEL WEATHERHEAD
  150186. SYNLETT
  150187. ZClSMADJA REVIEW RADICAL STEREOCHEM DIASTEREOSELECTIVE FELKIN ANH CRAM TRANSITION STATE STEREOELECTRONIC CHIRALM
  150188. 6870N
  150189. 2/28/96VgACYCLIC DIASTEREOFACIAL SELECTION IN INTERMOLECULAR RADICAL REACTIONS STERIC VERSUS ELECTRONIC CONTROLSW
  150190. 1994 P 1a
  150191. GABRIEL WEATHERHEAD
  150192. ACC CHEM RESChRIGBY TRANSITION METAL HIGHER ORDER 6+4 CYCLOADDITION CHROMIUM TARGET REVIEW TROPONE PHOTOCHEM CATALYTICM
  150193. 6871N
  150194. 2/28/96VSTRANSITION METAL PROMOTED HIGHER ORDER CYCLOADDITION REACTIONS IN ORGANIC SYNTHESISW
  150195. VOL 26 1993 P 579a
  150196. GABRIEL WEATHERHEAD
  150197. Tet. Lett.CAPEI REDUCTION AZIDE AMINE HYDRIDE REDUCING AGENT ISOXAZOLE REVIEWM
  150198. 6872N
  150199. 2/28/96VPA FACILE AND CHEMOSELECTIVE REDUCTION OF AZIDE TO AMINE USING SODIUM BOROHYDRIDEW
  150200. 1993 P 7509a
  150201. GABRIEL WEATHERHEAD
  150202. J ORG CHEMCYFALCK SULFONE BIS BISSULFONE REDUCTION WRITING NIH REVIEW LITERATURE CARBANION ALKYLATIONM
  150203. 6873N
  150204. 2/28/96
  150205. ]VoSTEREOSPECIFIC DEHYDRATIVE ALKYLATION OF BIS SULFONES.  REDUCTION AND CHEMISTRY OF BIS PHENYLSULFONYL COMPOUNDSW
  150206. VOL 58 1993 P 5892a
  150207. GABRIEL WEATHERHEAD
  150208. SYNLETTC
  150209. ACYLDIHYDROPYRIDONES GRIGNARD
  150210. REAGENTS TITANIUM REAGENTS ORTHO
  150211. METALATION DIRECTED LITHIATION AROMATIC
  150212. ALDEHYDES INSITU PROTECTION KETONES BROMOBENZALDEHYDES CALICHEAMICINONE COMINS DLM
  150213. 6874N
  150214. 2/28/96V/THE SYNTHETIC UTILITY OF ALPHA
  150215. AMINO ALKOXIDES.W
  150216. 1992 AUGX
  150217. GABRIEL WEATHERHEAD
  150218. SYNLETT
  150219. 4HETEROCYCLIC RING
  150220. SYSTEMS MARINE NATURAL
  150221. PRODUCTS CIS
  150222. ETHYL
  150223. FORMYL
  150224. 3,4,7,8
  150225. DIHYDRO
  150226. OXOCIN
  150227. ONE 3
  150228. ETHYLENE ACETAL CONCISE TOTAL SYNTHESIS RED TIDE ORGANISM STEREOSELECTIVE REDUCTION CARBONYL
  150229. COMPOUNDS ZINC BOROHYDRIDE (+)
  150230. (S,S)
  150231. METHYLTETRAHYDROPYRAN
  150232. YL)ACETIC ACID CIVET CONSTITUENT KOTSUKI H
  150233. 6875N
  150234. 2/28/96VlBICYCLIC KETALS 
  150235.  VERSATILE INTERMEDIATES FOR THE STEREOCONTROLLED CONSTRUCTION OF CYCLIC ETHER DERIVATIVES.W
  150236. 1992 FEBX
  150237. GABRIEL WEATHERHEAD
  150238. SYNLETTC
  150239. ORGANIC
  150240. SYNTHESIS SILYLATIVE DECARBONYLATION CONVENIENT SYNTHESIS BOND FORMATION HALIDES REAGENTS ORGANOSTANNANES SALTS ROUTE ORGANOFLUOROSILICATES HATANAKA YM
  150241. 6876N
  150242. 2/28/96VwHIGHLY SELECTIVE CROSS
  150243. COUPLING REACTIONS OF ORGANOSILICON COMPOUNDS MEDIATED BY FLUORIDE ION AND A PALLADIUM CATALYST.W
  150244. 1991 DECX
  150245. (12)a
  150246. GABRIEL WEATHERHEAD
  150247. SYNLETTC
  150248. PREPARING ALPHA
  150249. LITHIOSILANES 1
  150250. BROMOCYCLOPROPYLTRIMETHYLSILANE DERIVATIVES TRIARYLSILYLMETHYLMETALLIC REAGENTS GENERAL PROCEDURE CHELATION CONTROL LOBESIA
  150251. BOTRANA BOMBYX
  150252. MORI ALDEHYDES VINYLSILANES PHEROMONES BARRETT AGMM
  150253. 6877N
  150254. 2/28/96V4RECENT STUDIES ON THE PETERSON OLEFINATION REACTION.W
  150255. 1991 NOVX
  150256. (11)a
  150257. GABRIEL WEATHERHEAD
  150258. J ORG CHEMCaNAKAMURA FELKIN
  150259. ANh CRAM CHELATION ZINC COPPER DIASTEREOSELECTIVE WRITING REVIEW ALLYLATION METALM
  150260. 6878N
  150261. 2/28/96
  150262. bVW1,2
  150263. ASYMMETRIC INDUCTION IN THE SN2' ALLYLATION OF ORGANOCOPPER AND ORGANOZINC REAGENTSW
  150264. VOL 58 1993 P 5121a
  150265. GABRIEL WEATHERHEAD
  150266. SYNLETTCpHEANEY TRIFLATE REVIEW TRIMETHYLSILYL SILICON CATALYST FLUOROSULFONATE INTRODUCTION LIPSHUTZ PREPARATION SEMONESM
  150267. 6879N
  150268. 2/28/96V^A CONVENIENT ALTERNATIVE ROUTE TO TRIMETHYLSILYLFLUOROSULFONATE FOR SUE IN CATALYTIC REACTIONSW
  150269. 1993 P 583a
  150270. GABRIEL WEATHERHEAD
  150271. ACC CHEM RESC
  150272. JOHNSON BALDWIN RULES DUNITZ TRAJECTORY EXO ENDO DIG TRIG KEITH STUDENT WRITING ALKYNE INTRAMOLECULAR CYCLIZATION STEREOELECTRONIC REVIEW ALKOXIDE GEOMETRYM
  150273. 6880N
  150274. 2/28/96VfSTEREOELECTRONIC EFFECTS IN THE FORMATION OF FIVE AND SIX MEMBERED RINGS.  THE ROLE OF BALDWIN'S RULESW
  150275. VOL 26 1993 P 476a
  150276. GABRIEL WEATHERHEAD
  150277. Tet. Lett.CxKUWAJIMA CYCLOPENTANE 3+2 ZWITTERION SILYL ENOL ETHER CYCLOPROPANE CYCLOADDITION THIO LEWIS ACID TRANSITION STATE REVIEWM
  150278. 6881N
  150279. 2/28/96
  150280. DIASTEREOSELECTIVE 3+2 CYCLOADDITION OF 2
  150281. PHENYLTHIOCYCLOPROPYL KETONE WITH ENOL SILYL ETHERS.  SYNTHESIS OF FUNCTIONALIZED CYCLOPENTENESW
  150282. 1993 P 6077a
  150283. GABRIEL WEATHERHEAD
  150284. 6882N
  150285. 2/28/96VjWEISSERMEL, KLAUS; ARPE, HANS
  150286. JURGEN. INDUSTRIAL ORGANIC CHEMISTRY, 2ND ED.; VCH: NEW YORK, 1993. A REVIEWa
  150287. GABRIEL WEATHERHEAD
  150288. 6883N
  150289. 2/28/96V
  150290. STRUKUL, GEORGIO, ED. CATALYTIC OXIDATIONS WITH HYDROGEN PEROXIDE AS OXIDANT. KLUWER ACADEMIC PUBL.:DORDRECHT, THE NETHERLANDS, 1992. A REVIEWa
  150291. GABRIEL WEATHERHEAD
  150292. 6884N
  150293. 2/28/96VqSMITH, K., ED. SOLID SUPPORTS AND CATALYSTS IN ORGANIC SYNTHESIS. ELLIS HORWOOD: CHICHESTER, U.K., 1992. A REVIEWa
  150294. GABRIEL WEATHERHEAD
  150295. 6885N
  150296. 2/28/96V
  150297. SANDLER, STANLEY R.; KARO, WOLF. SOURCEBOOK OF ADVANCED ORGANIC LABORATORY PREPARATIONS. ACADEMIC: SAN DIEGO, CA, 1992. A REVIEWa
  150298. GABRIEL WEATHERHEAD
  150299. 6886N
  150300. 2/28/96
  150301. jVuRAHMAN, ATTA
  150302. UR; SHAH, ZAHIR. STEREOSELECTIVE SYNTHESIS IN ORGANIC CHEMISTRY. SPRINGER
  150303. VERLAG: BERLIN, 1993. A REVIEWa
  150304. GABRIEL WEATHERHEAD
  150305. 6887N
  150306. 2/28/96V
  150307. RAHMAN, ATTA
  150308. UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 11: STEREOSELECTIVE SYNTHESIS, PART G. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1992. A REVIEWa
  150309. GABRIEL WEATHERHEAD
  150310. 6888N
  150311. 2/28/96V
  150312. RAHMAN, ATTA
  150313. UR; BASHA, FATIMA A., EDS. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 13: BIOACTIVE NATURAL PRODUCTS, PART A. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1993. A REVIEWa
  150314. GABRIEL WEATHERHEAD
  150315. 6889N
  150316. 2/28/96V
  150317. PETERS, K. E.; MOLDOWAN, J. M. THE BIOMARKER GUIDE: INTERPRETING MOLECULAR FOSSILS IN PETROLEUM AND ANCIENT SEDIMENTS. PRENTICE HALL: ENGLEWOOD CLIFF, NJ, 1993. A REVIEWa
  150318. GABRIEL WEATHERHEAD
  150319. 6890N
  150320. 2/28/96
  150321. PATAI, SAUL, ED. SUPPLEMENT B: THE CHEMISTRY OF ACID DERIVATIVES, VOL. 2, PART 2 (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1992. A REVIEWa
  150322. GABRIEL WEATHERHEAD
  150323. 6891N
  150324. 2/28/96VyPAGE, MICHAEL I., ED. THE CHEMISTRY OF ,B
  150325. LACTAMS.BLACKIE ACADEMIC & PROFESSIONAL/CHAPMAN AND HALL:LONDON, 1992. A REVIEWa
  150326. GABRIEL WEATHERHEAD
  150327. 6892N
  150328. 2/28/96V
  150329. OKI, MICHINORI. CHEMISTRY OF ROTATIONAL ISOMERS. (REACTIVITY AND STRUCTURE, VOL. 31). SPRINGER
  150330. VERLAG: BERLIN, GERMANY, 1993. A REVIEWa
  150331. GABRIEL WEATHERHEAD
  150332. 6893N
  150333. 2/28/96V
  150334. MARK, HERMAN. FROM SMALL MOLECULES TO LARGE: A CENTURY OF PROGRESS. (PROFILES, PATHWAYS AND DREAMS:AUTOBIOGRAPHIES OF EMINENT CHEMISTS, JEFFREY I. SEEMAN,ED.) AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1993. A REVIEWa
  150335. GABRIEL WEATHERHEAD
  150336. 6894N
  150337. 2/28/96VnKLESSINGER, M.; MICHL, J. EXCITED STATES AND PHOTOCHEMISTRY OF ORGANIC MOLECULES. VCH: NEW YORK,1993. A REVIEW
  150338. GABRIEL WEATHERHEAD
  150339. 6895N
  150340. 2/28/96VcKAGAN,JACQUES. ORGANICPHOTOCHEMISTRY. PRINCIPLES AND APPLICATIONS. ACADEMIC: LONDON, 1993. A REVIEWa
  150341. GABRIEL WEATHERHEAD
  150342. 6896N
  150343. 2/28/96V
  150344. GOLDBERG, YURI. PHASE TRANSFER CATALYSIS. SELECTED PROBLEMS AND APPLICATIONS. GORDON AND BREACH: PHILADELPHIA, PA, 1992. A REVIEWa
  150345. GABRIEL WEATHERHEAD
  150346. 6897N
  150347. 2/28/96V
  150348. FURIN, G. G. SYNTHETIC ASPECTS OF THE FLUORINATION OF ORGANIC COMPOUNDS. HARWOOD ACADEMIC PUBL.: READING, BERKSHIRE, U.K., 1991. A REVIEWa
  150349. GABRIEL WEATHERHEAD
  150350. 6898N
  150351. 2/28/96V^DEHMLOW, E. V.; DEHMLOW, S. S. PHASE TRANSFER CATALYSIS, 3RD ED. VCH: NEW YORK, 1993. A REVIEWa
  150352. GABRIEL WEATHERHEAD
  150353. 6899N
  150354. 2/28/96VZCINTAS, P. ACTIVATED METALS IN ORGANIC SYNTHESIS.CRC PRESS: BOCA RATON, FL, 1993. A REVIEWa
  150355. GABRIEL WEATHERHEAD
  150356. 6900N
  150357. 2/28/96
  150358. BRADSHAW, JERALD S.; KRAKOWIAK, KRZYSZTOF E.; IZATT, REED M. AZA
  150359. CROWN MACROCYCLES. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 51). WILEY: NEW YORK,1993. A REVIEWa
  150360. GABRIEL WEATHERHEAD
  150361. 6901N
  150362. 2/28/96VdBILLUPS, W. EDWARD; CIUFOLINI, MARCO A., EDS. BUCKMINSTERFULLERENENES. VCH: NEW YORK, 1993. A REVIEWa
  150363. GABRIEL WEATHERHEAD
  150364. 6902N
  150365. 2/28/96V
  150366. BEMILLER, JAMES N.; WHISTLER, ROY L.; SHAW, DERIK H, EDS. LIPOPOLYSACCHARIDES, SEPARATION AND ANALYSIS, GLYCOSYLATED POLYMERS (METHODS IN CARBOHYDRATE CHEMISTRY, VOL. 9). WILEY: NEW YORK, 1993. A REVIEWa
  150367. GABRIEL WEATHERHEAD
  150368. 6903N
  150369. 2/28/96VaANON. THE BRANDON AMINO ACID AND PEPTIDE GUIDE. BRANDON ASSOCIATES, MERRIMACK, NH, 1992. A REVIEWa
  150370. GABRIEL WEATHERHEAD
  150371. 6904N
  150372. 2/28/96VLANDO, WATARU, ED. ORGANIC PEROXIDES. WILEY: CHICHESTER, U.K., 1992. A REVIEWa
  150373. GABRIEL WEATHERHEAD
  150374. 6905N
  150375. 2/28/96
  150376. AITKEN, R. A.; KILENYI, S. N., EDS. ASYMMETRIC SYNTHESIS. BLACKIE ACADEMIC & PROFESSIONAL/CHAPMAN AND HALL: LONDON, 1992. A REVIEWa
  150377. GABRIEL WEATHERHEAD
  150378. 6906N
  150379. 2/28/96
  150380. TOMALIA, DONALD A.; DURST, H. DUPONT. GENEALOGICALLY DIRECTED SYNTHESIS: STARBURST/CASCADE DENDRIMERS AND HYPERBRANCHED STRUCTURES.  TOPICS IN CURRENT CHEMISTRY 1993,165 (SUPRAMOLECULAR CHEMISTRY DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION), 193
  150381. 313. A REVIEW
  150382. GABRIEL WEATHERHEAD
  150383. 6907N
  150384. 2/28/96V
  150385. MISUMI, SOICHI. RECOGNITORY COLORATION OF CATIONS WITH CHROMOCARCERANDS.  TOPICS IN CURRENT CHEMISTRY 1993,165 (SUPRAMOLECULAR CHEMISTRY I
  150386. DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION), 163
  150387. 192. A REVIEWa
  150388. GABRIEL WEATHERHEAD
  150389. 6908N
  150390. 2/28/96
  150391. CHAMBRON, JEAN
  150392. CLAUDE; DIETRICH
  150393. BUCHECKER, CHRISTIANE; SAUVAGE, JEAN
  150394. PIERRE. FROM CLASICAL CHIRALITY TO TOPOLOGICALLY CHIRAL CATENANDS AND KNOTS.  TOPICS IN CURRENT CHEMISTRY 1993,165 (SUPRAMOLECULAR CHEMISTRY I
  150395. DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION), 131
  150396. 162. A REVIEW
  150397. GABRIEL WEATHERHEAD
  150398. 6909N
  150399. 2/28/96
  150400. PCOLLET, ANDRE; DUTASTA, JEAN
  150401. PIERRE; LOZACH, BENEDICTE; CANCEILL, JOSETTE. CYCLOTRIVERATRYLENES AND CRYPTOPHANES: THEIR SYNTHESIS AND APPLICATIONS TO HOST
  150402. GUEST CHEMISTRY AND TO THE DESIGN OF NEW MATERIALS.  TOPICS IN CURRENT CHEMISTRY 1993, 165 (SUPRAMOLECULAR CHEMISTRY DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION), 103
  150403. 129. A REVIEW
  150404. GABRIEL WEATHERHEAD
  150405. 6910N
  150406. 2/28/96V
  150407. ZIMMERMAN, STEVEN C. RIGID MOLECULAR TWEEZERS AS HOSTS FOR THE COMPLEXATION OF NEUTRAL GUESTS.  TOPICS IN CURRENT CHEMISTRY 1993,165 (SUPRAMOLECULAR CHEMISTRY I
  150408. DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION), 71
  150409. 102. A REVIEW
  150410. GABRIEL WEATHERHEAD
  150411. 6911N
  150412. 2/28/96
  150413. ;KOHNKE, FRANZ H.; MATHIAS, JOHN P.; STODDART, J. FRASER. SUBSTRATE
  150414. DIRECTED SYNTHESIS: THE RAPID ASSEMBLY OF NOVEL MACROPOLYCYCLIC STRUCTURES VIA STEREOREGULAR DIELS
  150415. ALDER OLIGOMERIZATION.  TOPICS IN CURRENT CHEMISTRY 1993,165 (SUPRAMOLECULAR CHEMISTRY I
  150416. DIRECTED SYNTHESIS AND MOLECULAR RECOGNITION),1
  150417. 69. A REVIEW
  150418. GABRIEL WEATHERHEAD
  150419. 6912N
  150420. 2/28/96V
  150421. ROTH, HEINZ D. STRUCTURE AND REACTIVITY OF ORGANIC RADICAL CATIONS.  TOPICS IN CURRENT CHEMISTRY 1992,163 (PHOTOINDUCED ELECTRON TRANSFER IV), 131
  150422. 245. A REVIEWa
  150423. GABRIEL WEATHERHEAD
  150424. 6913N
  150425. 2/28/96V
  150426. ZAMARAEV, K. I.; KHAIRUTDINOV, R. F. PHOTOINDUCED ELECTRON TUNNELING REACTIONS IN CHEMISTRY AND BIOLOGY.  TOPICS IN CURRENT CHEMISTRY 1992, 163 (PHOTOINDUCED ELECTRON TRANSFER IV) 1
  150427. 94. A REVIEWa
  150428. GABRIEL WEATHERHEAD
  150429. 6914N
  150430. 2/28/96
  150431. SALOMON, CLAUDIO,; MATA, ERNESTO G.. RECENT DEVELOPMENTS IN CHEMICAL DEPROTECTION OF ESTER FUNCTIONALGROUPS.  TETRAHEDRON 1993,49(18),3691
  150432. 3748. A REVIEWa
  150433. GABRIEL WEATHERHEAD
  150434. 6915N
  150435. 2/28/96VjGORBATENKO, VICTOR I. CHEMISTRY OF CHLOROCARBONYL ISOCYANATE.  TETRAHEDRON 1993, 49(16), 3227
  150436. 57. A REVIEWa
  150437. GABRIEL WEATHERHEAD
  150438. 6916N
  150439. 2/28/96V
  150440. BEAUCAGE, SERGE L.; IYER, RADHAKRISHNAN P. THE FUNCTIONALIZATION OF OLIGONUCLEOTIDES VIA PHOSPHORAMIDITE DERIVATIVES. TETRAHEDRON. 1993, 49(10),1925
  150441. 63. A REVIEWa
  150442. GABRIEL WEATHERHEAD
  150443. 6917N
  150444. 2/28/96V
  150445. LUH, TIEN
  150446. YAU; WONG, KEN
  150447. TSUNG. SILYL
  150448. SUBSTITUTED CONJUGATED DIENES: VERSATILE BUILDING BLOCKS OF ORGANIC SYNTHESIS.  SYNTHESIS 1993, (4), 349
  150449. 70. A REVIEWa
  150450. GABRIEL WEATHERHEAD
  150451. 6918N
  150452. 2/28/96V[ALBINI, ANGELO. SYNTHETIC UTILITY OF AMINE N
  150453. OXIDES.  SYNTHESIS 1993, (3), 263
  150454. 77. A REVIEWa
  150455. GABRIEL WEATHERHEAD
  150456. 6919N
  150457. 2/28/96
  150458. CAMPBELL, M. M.; SAINSBURY, M.; SEARLE, P. A. THE BIOSYNTHESIS AND SYNTHESIS OF SHIKIMIC ACID, CHORISMIC ACID, AND RELATED COMPOUNDS.  SYNTHESIS 1993, (2),179
  150459. 93. A REVIEWa
  150460. GABRIEL WEATHERHEAD
  150461. 6920N
  150462. 2/28/96VjZIMMER,REINHOLD. ALKOXYALLENES
  150463. BUILDING BLOCKS IN ORGANIC SYNTHESIS.  SYNTHESIS 1993, (2),165
  150464. 78. A REVIEWa
  150465. GABRIEL WEATHERHEAD
  150466. 6921N
  150467. 2/28/96V
  150468. BLACK, DAVID ST. C. NEW DIMENSIONS IN INDOLE CHEMISTRY: FROM LIGAND DESIGN TO NATURAL PRODUCTS.  SYNLETT 1993,(4),246
  150469. 52. A REVIEWa
  150470. GABRIEL WEATHERHEAD
  150471. 6922N
  150472. 2/28/96V
  150473. GOLEBIOWSKI, ADAM; JURCZAK, JANUSZ. A
  150474. AMINO
  150475. HYDROXY ACIDS IN THE TOTAL SYNTHESIS OF AMINO SUGARS.  SYNLETT 1993,(4),241
  150476. 5. A REVIEWa
  150477. GABRIEL WEATHERHEAD
  150478. 6923N
  150479. 2/28/96V
  150480. LAUTENS, MARK. RING OPENING REACTIONS OF OXABICYCLIC COMPOUNDS AS A ROUTE TO CYCLIC AND ACYCLIC COMPOUNDS WITH MULTIPLE STEREOCENTERS.  SYNLETT 1993, (3), 177
  150481. 85. A REVIEWa
  150482. GABRIEL WEATHERHEAD
  150483. 6924N
  150484. 2/28/96V
  150485. BENNETAU, BERNARD; DUNOGUES, JACQUES. UNUSUAL ELECTROPHILIC SUBSTITUTION IN THE AROMATIC SERIES VIA ORGANOSILICON INTERMEDIATES.  SYNLETT 1993, (3),171
  150486. 6. A REVIEWa
  150487. GABRIEL WEATHERHEAD
  150488. 6925N
  150489. 2/28/96V
  150490. BROOK, MICHAEL A.; HENRY, COURTNEY; JUESCHKKE, RALF; MODI, PANKAJ. BALANCING LEAVING GROUP ABILITY AND THE ,B
  150491. EFFECT: EXPLORING THE SYNTHETIC UTILITY OF CHLOROSILYL GROUPS.  SYNLETT 1993,(2),97
  150492. 104. A REVIEWa
  150493. GABRIEL WEATHERHEAD
  150494. 6926N
  150495. 2/28/96V
  150496. UNO, HIDEMITSU; SUZUKIB, HITOMI. NUCLEOPHILIC PERFLUOROALKYLATION USING PERFLUOROALKYLLITHIUMS.  SYNLETT 1993, (2),91
  150497. 6. A REVIEWa
  150498. GABRIEL WEATHERHEAD
  150499. 6927N
  150500. 2/28/96V
  150501. LE GUILLANTON, GEORGES. ELECTROCHEMICAL ACTIVATION OF SULFUR IN ORGANIC SOLVENTS
  150502. NEW SYNTHESES OF THIOORGANIC COMPOUNDS WITH A SACRIFICIAL CARBON
  150503. SULFUR ELECTRODE.  SULFUR REPORTS 1992, 12(2), 405
  150504. 35. A REVIEWa
  150505. GABRIEL WEATHERHEAD
  150506. 6928N
  150507. 2/28/96
  150508. VnRAO, V. PUSHKARA. THE PHOTOREACTIVITY OF THIOCARBONYL COMPOUNDS.  SULFUR REPORTS 1992,12(2), 359
  150509. 403. A REVIEWa
  150510. GABRIEL WEATHERHEAD
  150511. 6929N
  150512. 2/28/96VtGHOSH, TIRTHANKAR. REACTION OF CARBENES WITH DIVALENT SULFUR COMPOUNDS.  SULFUR REPORTS 1992,12(2), 339
  150513. 57. A REVIEWa
  150514. GABRIEL WEATHERHEAD
  150515. 6930N
  150516. 2/28/96V
  150517. BRILLON, DENIS. RECENT DEVELOPMENTS IN THE AREA OF THIONATION METHODS AND RELATED SYNTHETIC APPLICATIONS.  SULFUR REPORTS 1992,12(2),297
  150518. 338. A REVIEWa
  150519. GABRIEL WEATHERHEAD
  150520. 6931N
  150521. 2/28/96V
  150522. DRABOWICZ, JOZEF; KIELBASINSKI, PIOTR; LYZWA, PIOTR. STEREOSELECTIVE REACTIONS AT THE A
  150523. CARBON ATOM IN ORGANOSULFUR COMPOUNDS.  SULFUR REPORTS 1992,12(2), 213
  150524. 96. A REVIEWa
  150525. GABRIEL WEATHERHEAD
  150526. 6932N
  150527. 2/28/96VWJAEGER, L.; KOEHLER, H. PSEUDOCHALCOGENS.  SULFUR REPORTS 1992, 12(2),159
  150528. 212. A REVIEWa
  150529. GABRIEL WEATHERHEAD
  150530. 6933N
  150531. 2/28/96
  150532. USOV, V. A.; TIMOKHINA, L. V.; VORONKOV, M. G. THIOFORMYL COMPOUNDS. SYNTHESIS, STRUCTURE AND PROPERTIES.  SULFUR REPORTS 1992, 12(2), 95
  150533. 158. A REVIEWa
  150534. GABRIEL WEATHERHEAD
  150535. 6934N
  150536. 2/28/96VkPYNE, STEPHEN G. DIASTEREOSELECTIVE REACTIONS OF SULFOXIMINES.  SULFUR REPORTS 1992, 12(1), 57
  150537. 89. A REVIEWa
  150538. GABRIEL WEATHERHEAD
  150539. 6935N
  150540. 2/28/96V
  150541. TROFIMOV, B. A.; SOKOLYANSKAYA, L. V.; SENNING, A. DIVINYL DISULFIDES: SYNTHESIS AND PROPERTIES.  SULFUR REPORTS 1992, 12(1),1
  150542. 50. A REVIEWa
  150543. GABRIEL WEATHERHEAD
  150544. 6936N
  150545. 2/28/96V
  150546. MARSHALL, W. S.; CARUTHERS, M. H. PHOSPHORODITHIOATE DNA AS A POTENTIAL THERAPEUTIC DRUG.  SCIENCE (WASHINGTON, D.C. 1883
  150547. ) 1993, 259(5101), 1564
  150548. 70. A REVIEWa
  150549. GABRIEL WEATHERHEAD
  150550. 6937N
  150551. 2/28/96VlCASEY, CHARLES P. ORGANORHENIUM CHEMISTRY.  SCIENCE (WASHINGTON, D.C. 1883
  150552. ) 1993,259(5101),1552
  150553. 8. A REVIEWa
  150554. GABRIEL WEATHERHEAD
  150555. 6938N
  150556. 2/28/96
  150557. NUGENT, WILLIAM A.; RAJANBABU, T. V.; BURK, MARK J. BEYOND NATURE'S CHIRAL POOL: ENANTIOSELECTIVE CATALYSIS IN INDUSTRY.  SCIENCE (WASHINGTON, D.C. 1883
  150558. ) 1993, 259(5094), 479
  150559. 83. A REVIEWa
  150560. GABRIEL WEATHERHEAD
  150561. 6939N
  150562. 2/28/96V
  150563. BARANOV, G. M.; PEREKALIN, V. V. ALIPHATIC ORGANOPHOSPHORUS NITRO
  150564. COMPOUNDS.  RUSSIAN CHEMICAL REVIEWS 1992, 61(12),1220. A REVIEWa
  150565. GABRIEL WEATHERHEAD
  150566. 6940N
  150567. 2/28/96V
  150568. SADOVA, N. I.; KHAIKIN, L. S.; VILKOV, L. V. SOME PROBLEMS IN THE STEREOCHEMISTRY OF NITROGEN COMPOUNDS IN THE GAS PHASE.  RUSSIAN CHEMICAL REVIEWS 1992, 61(12),1169. A REVIEWa
  150569. GABRIEL WEATHERHEAD
  150570. 6941N
  150571. 2/28/96V
  150572. KHARITONOV, A. S.; SOBOLEV, V. I.; PANOV, G. I. HYDROXYLATYION OF AROMATIC COMPOUNDS WITH NITROUS OXIDE.NEW POSSIBILITIES OF OXIDATIVE CATALYSTS ON ZEOLITES.  RUSSIAN CHEMICAL REVIEWS 1992,61(11), 1130. A REVIEWa
  150573. GABRIEL WEATHERHEAD
  150574. 6942N
  150575. 2/28/96
  150576. KRYLOV, O. V. THE PARTIAL CATALYTIC OXIDATION OF METHANE TO GIVE OXYGEN
  150577. CONTAINING COMPOUNDS.  RUSSIAN CHEMICAL REVIEWS 1992, 61(11),1118. A REVIEWa
  150578. GABRIEL WEATHERHEAD
  150579. 6943N
  150580. 2/28/96V
  150581. STADNICHUK, M. D.; VOROPAEVA, T. I. SILICON
  150582.  CONTAINING 1,3
  150583. ALKENYNES AND MORE UNSATURATED COMPOUNDS.  RUSSIAN CHEMICAL REVIEWS 1992, 61(11), 1091. A REVIEWa
  150584. GABRIEL WEATHERHEAD
  150585. 6944N
  150586. 2/28/96V
  150587. GATILOV, YU. V.; BARKHASH, V. A. INVESTIGATION OF MOLECULAR CARBONIUM ION REARRANGEMENTS BY THE MOLECULAR MECHANICS METHODS.  RUSSIAN CHEMICAL REVIEWS 1992, 61(11),1077. A REVIEWa
  150588. GABRIEL WEATHERHEAD
  150589. 6945N
  150590. 2/28/96V
  150591. TURUTA, A. M.; VOISHVILLO, N. E.; KAMERNETSKII, A. V. MICROBIOLOGICAL HYDROXYLATION OF 5A
  150592. STEROIDS.  RUSSIAN CHEMICAL REVIEWS 1992, 61 (10),1033. A REVIEWa
  150593. GABRIEL WEATHERHEAD
  150594. 6946N
  150595. 2/28/96
  150596. CHVERTKINA, L. V.; KHOKLOV, P. S.; MIRONOV, V. F. PHOSPHORUS DERIVATIVES OF SALICYLIC ACID.  RUSSIAN CHEMICAL REVIEWS 1992, 61(10),1009. A REVIEWa
  150597. GABRIEL WEATHERHEAD
  150598. 6947N
  150599. 2/28/96V
  150600. AKULOV, P. KINETIC ISOTOPE EFFECTS IN THE ENZYMIC REACTIONS OF TRITIUM
  150601.  AND DEUTERIUM
  150602. CONTAINING SUBSTRATES.  RUSSIAN CHEMICAL REVIEWS 1992, 61 (10), 999. A REVIEWa
  150603. GABRIEL WEATHERHEAD
  150604. 6948N
  150605. 2/28/96V
  150606. VERWEIJ, JAN; DE, VROOM ERIK. INDUSTRIAL TRANSFORMATIONS OF PENICILLINS AND CEPHALOSPORINS.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150607. BAS 1993, 112 (2), 66
  150608. 81. A REVIEWa
  150609. GABRIEL WEATHERHEAD
  150610. 6949N
  150611. 2/28/96V
  150612. KOOMEN, G. J. SYNTHESIS AND BIOLOGICAL PROPERTIES OF SELECTED NUCLEOSIDE ANALOGS.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150613. BAS 1993, 112 (2), 51
  150614. 65. A REVIEWa
  150615. GABRIEL WEATHERHEAD
  150616. 6950N
  150617. 2/28/96
  150618. HENDRICKSON, JAMES B. DESCRIPTIONS OF REACTIONS: THEIR LOGIC AND APPLICATIONS.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150619. BAS 1992, 111 (6), 324
  150620. 35. A REVIEWa
  150621. GABRIEL WEATHERHEAD
  150622. 6951N
  150623. 2/28/96V
  150624. DOGANE, I.; TAKABATAKE, T.; BERSOHN, M. COMPUTER
  150625. EXECUTED SYNTHESIS PLANNING, A PROGRESS REPORT.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150626. BAS 1992, 111(6),291
  150627. 6. A REVIEWa
  150628. GABRIEL WEATHERHEAD
  150629. 6952N
  150630. 2/28/96V
  150631. GASTEIGER, J.; IHLENFELDT, W. D.; ROSE, P. A COLLECTION OF COMPUTER METHODS FOR SYNTHESIS DESIGN AND REACTION PREDICTION.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150632. BAS 1992,111(6), 270
  150633. 90. A REVIEWa
  150634. GABRIEL WEATHERHEAD
  150635. 6953N
  150636. 2/28/96V
  150637. DENGLER, ALF; FONTAIN, ERIC; KNAUER, MICHAEL; STEIN, NATALIE; UGI, IVAR. COMPETING CONCEPTS IN CAOS.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150638. BAS 1992, 111(6), 262
  150639. 9. A REVIEWa
  150640. GABRIEL WEATHERHEAD
  150641. 6954N
  150642. 2/28/96
  150643. OTT, MARTIN A.; NOORDIK, JAN H. COMPUTER TOOLS FOR REACTION RETRIEVAL AND SYNTHESIS PLANNING IN ORGANIC CHEMISTRY. A BRIEF REVIEW OF THEIR HISTORY, METHODS, AND PROGRAMS.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150644. BAS 1992,111(6), 239
  150645. 46. A REVIEWa
  150646. GABRIEL WEATHERHEAD
  150647. 6955N
  150648. 2/28/96V
  150649. LI, HAIFANG; LE NOBLE, WILLIAM J. COMPETING CONCEPTS IN ELECTRONIC CONTROL OF FACE SELECTION.  RECUEIL DES TRAVAUX CHIMIQUES DES PAYS
  150650. BAS 1992, 111(5), 199
  150651. 210. A REVIEWa
  150652. GABRIEL WEATHERHEAD
  150653. 6956N
  150654. 2/28/96V
  150655. BIEMANN, KLAUS. ANALYTICAL TECHNIQUES FOR TRACE ORGANIC COMPOUNDS
  150656. IV. TANDEM MASS SPECTROMETRY FOR ORGANIC TRACE ANALYSIS.  PURE AND APPLIED CHEMISTRY 1993, 65(5),1021
  150657. 7. A REVIEWa
  150658. GABRIEL WEATHERHEAD
  150659. 6957N
  150660. 2/28/96V
  150661. SAENGER, W.; NIEMANN, C.; HERBST, R.; HINRICHS, W.; STEINER, T. CRYSTAL STRUCTURES OF LINEAR AND CYCLIC OLIGOSACCHARIDES: AN OVERVIEW.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 809
  150662. 17. A REVIEWa
  150663. GABRIEL WEATHERHEAD
  150664. 6958N
  150665. 2/28/96V
  150666. GOTO, FUMITAKA; OGAWA, TOMOYA. RECENT ASPECTS OF GLYCOCONJUGATE SYNTHESIS: A SYNTHETIC APPROACH TO THE LINKAGE REGION OF PROTEOGLYCANS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 793
  150667. 801. A REVIEWa
  150668. GABRIEL WEATHERHEAD
  150669. 6959N
  150670. 2/28/96VnCONRAD, H. E. DISSECTION OF HEPARIN
  150671. PAST AND FUTURE.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 787
  150672. 91. A REVIEWa
  150673. GABRIEL WEATHERHEAD
  150674. 6960N
  150675. 2/28/96V
  150676. FRASER
  150677. REID, BERT; MERRITT, J. ROBERT; HANDLON, ANTHONY L.; ANDREWS, C. WEBSTER. THE CHEMISTRY OF N
  150678. PENTENYL GLYCOSIDES: SYNTHETIC, THEORETICAL, AND MECHANISTIC RAMIFICATIONS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 779
  150679. 86. A REVIEWa
  150680. GABRIEL WEATHERHEAD
  150681. 6961N
  150682. 2/28/96V
  150683. KISHI, YOSHITO. PREFERRED SOLUTION CONFORMATION OF MARINE NATURAL PRODUCT PALYTOXIN AND OF C
  150684. GLYCOSIDES AND THEIR PARENT GLYCOSIDES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 771
  150685. 8. A REVIEWa
  150686. GABRIEL WEATHERHEAD
  150687. 2/28/96V
  150688. ITO, YUKISHIGE; GAUDINO, JOHN J.; PAULSON, JAMES C. SYNTHESIS OF BIOACTIVE SIALOSIDES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 753
  150689. 62. A REVIEWa
  150690. GABRIEL WEATHERHEAD
  150691. 6963N
  150692. 2/28/96VyVASELLA, ANDREA. A NEW APPROACH TO THE SYNTHESIS OF GLYCOSIDES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 731
  150693. 52. A REVIEWa
  150694. GABRIEL WEATHERHEAD
  150695. 6964N
  150696. 2/28/96
  150697. SUSKA, ALINA; GRAJKOWSKI, ANDRZEJ; WILK, ANDRZEJ; UZNANSKI, BOGDAN; BLASZCZYK, JERZY; WIECZOREK, MICHAL; STEC, WOJCIECH J. ANTISENSE OLIGONUCLEOTIDES: STEREOCONTROLLED SYNTHESIS OF PHOSPHOROTHIOATE OLIGONUCLEOTIDES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 707
  150698. 14. A REVIEW
  150699. GABRIEL WEATHERHEAD
  150700. 6965N
  150701. 2/28/96V~SONODA,NOBORU. SELENIUM
  150702. ASSISTEDCARBONYLATION WITH CARBON MONOXIDE.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 699
  150703. 706. A REVIEWa
  150704. GABRIEL WEATHERHEAD
  150705. 6966N
  150706. 2/28/96
  150707. SCHMIDBAUR, HUBERT. SOME NEW CONCEPTS IN THE CHEMISTRY OF THE P
  150708. BLOCK ELEMENTS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 691
  150709. 8. A REVIEWa
  150710. GABRIEL WEATHERHEAD
  150711. 6967N
  150712. 2/28/96V
  150713. NAGASE, SHIGERU. THEORETICAL STUDY OF HETEROATOM
  150714. CONTAINING COMPOUNDS. FROM AROMATIC AND POLYCYCLIC MOLECULES TO HOLLOW CAGE CLUSTERS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 675
  150715. 82. A REVIEWa
  150716. GABRIEL WEATHERHEAD
  150717. 6968N
  150718. 2/28/96V
  150719. MARINO, J. P. ASYMMETRIC SYNTHESIS VIA OPTICALLY ACTIVE VINYL SULFOXIDES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 667
  150720. 74. A REVIEWa
  150721. GABRIEL WEATHERHEAD
  150722. 6969N
  150723. 2/28/96V
  150724. KIM, YONG HAE; LIM, SANG CHUL; KIM, KYUNG SU. ACTIVATION OF SUPEROXIDE: APPLICATION OF PEROXYSULFUR INTERMEDIATES TO ORGANIC SYNTHESIS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 661
  150725. 6. A REVIEWa
  150726. GABRIEL WEATHERHEAD
  150727. 6970N
  150728. 2/28/96
  150729. V|IMAMOTO, TSUNEO. SYNTHESIS AND REACTIONS OF NEW PHOSPHINE
  150730. BORANES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 655
  150731. 60. A REVIEWa
  150732. GABRIEL WEATHERHEAD
  150733. 6971N
  150734. 2/28/96
  150735. FREEMAN, RICHARD; HAYNES, RICHARD K.; LOUGHLIN, WENDY A.; MITCHELL, CRAIG; STOKES, JOHN V. SYNTHETIC UTILIZATION OF HIGHLY STEREOSELECTIVE CONJUGATE ADDITION REACTIONS OF PHOSPHORUS AND SULFUR STABILIZED ALLYLIC CARBANIONS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 647
  150736. 54. A REVIEW
  150737. GABRIEL WEATHERHEAD
  150738. 6972N
  150739. 2/28/96V
  150740. GARBESI, ANNA; GOTTARELLI, GIOVANNI; MARIANI, PAOLO; SPADA, GIAN PIERO. OLIGODEOXYGUANYLATES: A CASE OF SELF
  150741. ASSEMBLY LEADING TO LYOTROPIC LIQUID CRYSTALS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 641
  150742. 6. A REVIEWa
  150743. GABRIEL WEATHERHEAD
  150744. 6973N
  150745. 2/28/96V
  150746. BICKELHAUPT, FRIEDRICH. CARBENOID ROUTES TO SUBSTITUTED PHOSPHAALKENES AND PHOSPHABENZENES.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 621
  150747. 4. A REVIEWa
  150748. GABRIEL WEATHERHEAD
  150749. 6974N
  150750. 2/28/96V
  150751. BESTMANN, H. J. SYNTHESES AND REACTIONS OF MONO AND POLYELEMENTORGANIC COMPOUNDS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 617
  150752. 20. A REVIEWa
  150753. GABRIEL WEATHERHEAD
  150754. 6975N
  150755. 2/28/96V
  150756. BARTON, DEREK H. R.; PAREKH, SHYAMAL I. LIGAND COUPLING BASED ON HETEROATOM CHEMISTRY.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 603
  150757. 10. A REVIEWa
  150758. GABRIEL WEATHERHEAD
  150759. 6976N
  150760. 2/28/96V
  150761. BACHI, MARIO D.; BALANOV, ANNA; BAR
  150762. NER, NIRA; BOSCH, ERIC; DENENMARK, DANIELLA; MIZHIRITSKII, MICHAEL. SYNTHESIS OF NONAROMATIC HETEROCYCLIC COMPOUNDS THROUGH FREE
  150763. RADICAL REACTIONS.  PURE AND APPLIED CHEMISTRY 1993, 65(4), 595
  150764. 601. A REVIEWa
  150765. GABRIEL WEATHERHEAD
  150766. 6977N
  150767. 2/28/96V
  150768. CACCIAPAGLIA, ROBERTA; MANDOLINI, LUIGI. SPECIFIC TRANSITION STATE STABILIZATION BY METAL IONS IN REACTIONS OF FUNCTIONALIZED CROWN ETHERS.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 533
  150769. 8. A REVIEWa
  150770. GABRIEL WEATHERHEAD
  150771. 6978N
  150772. 2/28/96
  150773. LUENING, ULRICH; BAUMSTARK, ROLAND; WANGNIC CARSTEN; MUELLER, MICHAEL; SCHYJA, WOLFGANG; GERST, MATTHIAS; GELBERT, MARKUS. CONCAVE REAGENTS.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 527
  150774. 32. A REVIEWa
  150775. GABRIEL WEATHERHEAD
  150776. 6979N
  150777. 2/28/96V
  150778. KRAKOWIAK, KRZYSZTOF E.; BRADSHAW, JERALD S.; AN, HAOYUN; IZATT, REED M. SIMPLE METHODS FOR THE PREPARATION OF CRYPTANDS.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 511
  150779. 14. A REVIEWa
  150780. GABRIEL WEATHERHEAD
  150781. 6980N
  150782. 2/28/96V
  150783. ISNIN, RAHIMAH; KAIFER, ANGEL E. A NEW APPROACH TO CYCLODEXTRIN
  150784. BASED ROTAXANES.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 495
  150785. 8. A REVIEWa
  150786. GABRIEL WEATHERHEAD
  150787. 6981N
  150788. 2/28/96V
  150789. JEDLINSKI, Z. ALKALI METAL SUPRAMOLECULAR COMPLEXES AND THEIR SIGNIFICANCE IN ORGANIC CHEMISTRY.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 483
  150790. 8. A REVIEWa
  150791. GABRIEL WEATHERHEAD
  150792. 6982N
  150793. 2/28/96
  150794. HOLDT, H. J. THIACROWN COMPOUNDS WITH 1,2
  150795. DICYANO
  150796. DITHIOETHENE UNITS.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 477
  150797. 82. A REVIEWa
  150798. GABRIEL WEATHERHEAD
  150799. 6983N
  150800. 2/28/96
  150801. bDANIL DE NAMOR, ANGELA F.; BLACKETT, PETER M.; GARRIDO PARDO, MARIA T.; PACHECO TANAKA, DAVID A.; SUEROS VELARDE, FELIX J.; CABALEIRO, MERCEDES C. FROM MOLECULES TO ELECTROLYTES. ELECTROCHEMICAL AND THERMODYNAMIC ASPECTS OF THE INTERACTION OF PHENOL
  150802.  AND RESORCINOL
  150803. BASED CALIXARENES WITH AMINES.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 415
  150804. 22. A REVIEW
  150805. GABRIEL WEATHERHEAD
  150806. 6984N
  150807. 2/28/96V
  150808. BOEHMER, VOLKER; VOGT, WALTER. CALIX[4]ARENES, BRIDGED AT THE UPPER RIM.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 403
  150809. 8. A REVIEWa
  150810. GABRIEL WEATHERHEAD
  150811. 6985N
  150812. 2/28/96
  150813. SESSLER, JONATHAN L.; CYR, MICHAEL; FURUTA, HIROYUKI; KRAL, VLADIMIR; MODY, TARAK; MORISHIMA, TAKASHI; SHIONOYA, MITSUHIKO; WEGHORN, STEVEN. ANION BINDING: A NEW DIRECTION IN PORPHYRIN
  150814. RELATED RESEARCH.  PURE AND APPLIED CHEMISTRY 1993, 65(3),393
  150815. 8. A REVIEW
  150816. GABRIEL WEATHERHEAD
  150817. 6986N
  150818. 2/28/96V
  150819. VAN DIENST, ERIK; BAKKER, WOUTER I. IWEMA; ENGBERSEN, JOHAN F. J.; VERBOOM, WILLEM; REINHOUDT, DAVID N. CALIXARENES, CHEMICAL CHAMELEONS.  PURE AND APPLIED CHEMISTRY 1993, 65(3), 387
  150820. 92. A REVIEWa
  150821. GABRIEL WEATHERHEAD
  150822. 6987N
  150823. 2/28/96V
  150824. DANIL DE NAMOR, ANGELA F. THERMODYNAMICS OF SUPRAMOLECULAR SYSTEMS: RECENT DEVELOPMENTS.  PURE AND APPLIED CHEMISTRY 1993, 65(2), 193
  150825. 202. A REVIEWa
  150826. GABRIEL WEATHERHEAD
  150827. 6988N
  150828. 2/28/96V
  150829. YAMAMOTO, KOJI. EXTENDED SYSTEMS OF CLOSED HELICENE. SYNTHESIS AND CHARACTERIZATION OF [7] AND [7.7]
  150830. CIRCULENE. 1993, 65(1),157
  150831. 63. A REVIEWa
  150832. GABRIEL WEATHERHEAD
  150833. 2/28/96V`VOLLHARDT, K. PETER C. THE PHENYLENES.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 153
  150834. 56. A REVIEWa
  150835. GABRIEL WEATHERHEAD
  150836. 6990N
  150837. 2/28/96V
  150838. VOGEL, EMANUEL. THE PORPHYRINS FROM THE ANNULENE CHEMIST'S PERSPECTIVE.  PURE AND APPLIED CHEMISTRY 1993, 65(1),143
  150839. 52. A REVIEWa
  150840. GABRIEL WEATHERHEAD
  150841. 6991N
  150842. 2/28/96V
  150843. GIRRESER, ULRICH; GIUFFRIDA, DANIELE; KOHNKE, FRANZ H.; MATHIAS, JOHN P.; PHILP, DOUGLAS; STODDART, J. FRASER. THE STRUCTURE
  150844. DIRECTED SYNTHESIS OF CYCLACENE AND POLYACENE DERIVATIVES.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 119
  150845. 25. A REVIEWa
  150846. GABRIEL WEATHERHEAD
  150847. 6992N
  150848. 2/28/96V
  150849. RABINOVITZ, MORDECAI; AYALON, ARI. 1R
  150850. CONJUGATED POLYCYCLIC ANIONS; INTERPLAY BETWEEN TOPOLOGY, ELECTRONIC STRUCTURE AND PATTERNS OF CHARGE DISTRIBUTION.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 111
  150851. 18. A REVIEWa
  150852. GABRIEL WEATHERHEAD
  150853. 6993N
  150854. 2/28/96
  150855. MURATA, ICHIRO. NOVEL BONDING STRUCTURE OF SOME NONALTERNANT POLYCYCLIC SYSTEMS.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 97
  150856. 103. A REVIEWa
  150857. GABRIEL WEATHERHEAD
  150858. 6994N
  150859. 2/28/96V
  150860. LAI, YEE HING; CHEN, PU; PECK, THIAN GUAN. DIHYDROPYRENES: FURTHER INSIGHT INTO EFFECTS OF ANNULENOANNELATION, BENZANNELATION, CONJUGATION AND ISOANNELATION.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 81
  150861. 7. A REVIEWa
  150862. GABRIEL WEATHERHEAD
  150863. 6995N
  150864. 2/28/96V
  150865. HOPF, HENNING; WITULSKI, BERNHARD. CYANOALKYNES: MAGIC WANDS FOR THE PREPARATION OF NOVEL AROMATIC COMPOUNDS.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 47
  150866. 56. A REVIEWa
  150867. GABRIEL WEATHERHEAD
  150868. 6996N
  150869. 2/28/96VrHART, HAROLD. IPTYCENES, CUPPEDOPHANES AND CAPPEDOPHANES.  PURE AND APPLIED CHEMISTRY 1993, 65(1), 27
  150870. 34. A REVIEWa
  150871. GABRIEL WEATHERHEAD
  150872. 6997N
  150873. 2/28/96
  150874. HAYASHI, TAMIO; UOZUMI, YASUHIRO. CATALYTIC ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE ALCOHOLS VIA HYDROSILYLATION OF OLEFINS WITH A CHIRAL MONOPHOSPHINE
  150875. PALLADIUM CATALYST.  PURE AND APPLIED CHEMISTRY 1992, 64(12), 1911
  150876. 16. A REVIEWa
  150877. GABRIEL WEATHERHEAD
  150878. 6998N
  150879. 2/28/96V
  150880. DESLONGCHAMPS, PIERRE. TRANSANNULAR DIELS
  150881. ALDER REACTION ON MACROCYCLES. A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYCYCLIC COMPOUNDS.  PURE AND APPLIED CHEMISTRY 1992, 64(12),1831
  150882. 47. A REVIEWa
  150883. GABRIEL WEATHERHEAD
  150884. 6999N
  150885. 2/28/96V
  150886. KINGSTON, D. G. I.; MOLINERO, A. A.; RIMOLDI, J. M. THE TAXANE ALKALOIDS.  PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS 1993, 61,1
  150887. 192. A REVIEWa
  150888. GABRIEL WEATHERHEAD
  150889. 7000N
  150890. 2/28/96VzHARCOURT, RICHARD D. VALENCE BOND STRUCTURES AND ORGANIC CHEMISTRY.  NEW JOURNAL OF CHEMISTRY 1992,16(6), 667
  150891. 70. A REVIEWa
  150892. GABRIEL WEATHERHEAD
  150893. 7001N
  150894. 2/28/96
  150895. VpEPHRITIKHINE, MICHEL. RECENT ADVANCES IN ORGANOCHEMISTRY.  NEW JOURNAL OF CHEMISTRY 1992,16(4), 451
  150896. 69. A REVIEWa
  150897. GABRIEL WEATHERHEAD
  150898. 7002N
  150899. 2/28/96V
  150900. BADOR, PASCAL; SURREL, MARIE NOELLE. COMPUTER SYSTEMS FOR SEARCHING OF CHEMICAL REACTION DATABASES AND SYSTEMS FOR COMPUTER
  150901. AIDED DESIGN OF ORGANIC SYNTHESIS. NEW JOURNAL OF CHEMISTRY 1992, 16(3), 413
  150902. 23. A REVIEWa
  150903. GABRIEL WEATHERHEAD
  150904. 7003N
  150905. 2/28/96V
  150906. ASTRUC, DIDIER. TRANSITION METAL SANDWICHES AS RESERVOIRS OF ELECTRONS, PROTONS, HYDROGEN ATOMS AND HYDRIDES: MOLECULAR ACTIVATION AND ELECTRONICS.  NEW JOURNAL OF CHEMISTRY 1992,16(1
  150907. 2), 305
  150908. 28. A REVIEWa
  150909. GABRIEL WEATHERHEAD
  150910. 7004N
  150911. 2/28/96VuDIETRICH, BUCHECKER C.; SAUVAGE, J. P. SYNTHETIC MOLECULAR KNOTS.  NEW JOURNAL OF CHEMISTRY 16(1
  150912. 2), 277
  150913. 85. A REVIEWa
  150914. GABRIEL WEATHERHEAD
  150915. 7005N
  150916. 2/28/96
  150917. SHILOV, A. E. DINITROGEN FIXATION IN SOLUTION IN THE PRESENCE OF IRON COMPLEXES. INTERMEDIATES AND MECHANISM.  NEW JOURNAL OF CHEMISTRY 1992, 16(1
  150918. 2), 213
  150919. 18. A REVIEWa
  150920. GABRIEL WEATHERHEAD
  150921. 7006N
  150922. 2/28/96V
  150923. MEUNIER, BERNARD. POTASSIUM MONOPERSULFATE: JUST ANOTHER PRIMARY OXIDANT OR A HIGHLY VERSATILE OXYGEN ATOM DONOR IN METALLOPORPHYRIN
  150924. MEDIATED OXYGENATION AND OXIDATION REACTIONS.  NEW JOURNAL OF CHEMISTRY 1992, 16(1
  150925. 2), 203
  150926. 11. A REVIEWa
  150927. GABRIEL WEATHERHEAD
  150928. 7007N
  150929. 2/28/96V
  150930. EBERSON,LENNART. OUTER
  150931. SPHEREELECTRONTRANSFER REACTIONS, RARE EVENTS IN ORGANIC CHEMISTRY?  NEW JOURNAL OF CHEMISTRY 1992,16(1
  150932. 2), 151
  150933. 6. A REVIEWa
  150934. GABRIEL WEATHERHEAD
  150935. 7008N
  150936. 2/28/96VgFODOR, G.; DHARANIPRAGADA, R. TROPANE ALKALOIDS. NATURAL PRODUCT REPORTS 1993, 10(2), 199
  150937. 206. A REVIEWa
  150938. GABRIEL WEATHERHEAD
  150939. 7009N
  150940. 2/28/96VPHANSON, J. R. DITERPENOIDS.  NATURAL PRODUCT REPORTS 1993,10(2),159
  150941. 74. A REVIEW
  150942. GABRIEL WEATHERHEAD
  150943. 7010N
  150944. 2/28/96VpLEY,S.V.;DENHOLM,A.A.;WOOD,A. THECHEMISTRY OF AZADIRACHTIN.  NATURAL PRODUCT REPORTS 1993,10(2),109
  150945. 57. A REVIEWa
  150946. GABRIEL WEATHERHEAD
  150947. 7011N
  150948. 2/28/96VuMICHAEL, J. P. QUINOLINE, QUINAZOLINE, AND ACRIDONE ALKALOIDS.  NATURAL PRODUCT REPORTS 1993, 10(2), 99
  150949. 108. A REVIEWa
  150950. GABRIEL WEATHERHEAD
  150951. 7012N
  150952. 2/28/96VvDICKINSON, J. M. MICROBIAL PYRAN
  150953. ONES AND DIHYDROPYRAN
  150954. ONES.  NATURAL PRODUCT REPORTS 1993, 10(1), 71
  150955. 98. A REVIEWa
  150956. GABRIEL WEATHERHEAD
  150957. 7013N
  150958. 2/28/96VnMICHAEL, J. P. INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDS.  NATURAL PRODUCT REPORTS 1993, 10(1), 51
  150959. 70. A REVIEWa
  150960. GABRIEL WEATHERHEAD
  150961. 7014N
  150962. 2/28/96V
  150963. LEWIS, J. R. MUSCARINE, OXAZOLE, IMIDAZOLE, THIAZOLE, AND PEPTIDE ALKALOIDS AND OTHER MISCELLANEOUS ALKALOIDS.  NATURAL PRODUCT REPORTS 1993,10(1),29
  150964. 50. A REVIEWa
  150965. GABRIEL WEATHERHEAD
  150966. 7015N
  150967. 2/28/96
  150968. VlWARD, R. S. LIGNANS, NEOLIGNANS, AND RELATED COMPOUNDS.  NATURAL PRODUCT REPORTS 1993, 10(1), 1
  150969. 28. A REVIEWa
  150970. GABRIEL WEATHERHEAD
  150971. 7016N
  150972. 2/28/96V
  150973. CATSOULACOS, P.; CATSOULACOS, D. ON THE SYNTHESIS OF PYRIDO[3,2,1
  150974. KL]PHENOTHIAZINE, QUINO[8,1
  150975. BC] [1,4]
  150976. BENZOTHIAZEPINE AND THEIR DERIVATIVES.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(4), 675
  150977. 82. A REVIEWa
  150978. GABRIEL WEATHERHEAD
  150979. 7017N
  150980. 2/28/96V
  150981. SPECKAMP, W. N. NEW ASPECTS OF OLD REACTIONS. CATIONS AND RADICALS IN HETEROCYCLIC SYNTHESIS.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 653
  150982. 74. A REVIEWa
  150983. GABRIEL WEATHERHEAD
  150984. 7018N
  150985. 2/28/96V}REES, CHARLES W. POLYSULFUR
  150986. NITROGEN HETEROCYCLIC CHEMISTRY.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 639
  150987. 51. A REVIEWa
  150988. GABRIEL WEATHERHEAD
  150989. 7019N
  150990. 2/28/96V
  150991. WINTERFELDT,EKKEHARD. DIRECTEDSTEREOSELECTIVITY IN ALKALOID SYNTHESIS.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 631
  150992. 38. A REVIEW
  150993. GABRIEL WEATHERHEAD
  150994. 7020N
  150995. 2/28/96V
  150996. SHINKAI, ICHIRO. A PRACTICAL ASYMMETRIC SYNTHESIS OF A NOVEL TOPICALLY ACTIVE CARBONIC ANHYDRASE INHIBITOR.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 627
  150997. 30. A REVIEWa
  150998. GABRIEL WEATHERHEAD
  150999. 7021N
  151000. 2/28/96V
  151001. ISOBE, MINORU; NISHIKAWA, TOSHIO; YAMAMOTO, NOBORU; TSKIYAMA, TAKAHIRO; INO, AKIRA; OKITA, TAKAAKI. METHODOLOGIES FOR SYNTHESIS OF HETEROCYCLIC COMPOUNDS.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 619
  151002. 24. A REVIEWa
  151003. GABRIEL WEATHERHEAD
  151004. 7022N
  151005. 2/28/96V
  151006. PATTENDEN, GERALD. SYNTHETIC STUDIES WITH NATURAL OXAZOLES AND THIAZOLES.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 607
  151007. 18. A REVIEWa
  151008. GABRIEL WEATHERHEAD
  151009. 7023N
  151010. 2/28/96V
  151011. PFLEIDERER, WOLFGANG. PTERIDINES. PROPERTIES, REACTIVITIES, AND BIOLOGICAL SIGNIFICANCE.  JOURNAL OF HETEROCYCLIC CHEMISTRY 1992, 29(3), 583
  151012. 605. A REVIEWa
  151013. GABRIEL WEATHERHEAD
  151014. 7024N
  151015. 2/28/96
  151016. CHIMIRRI, ALBA; GITTO, ROSARIA; GRASSO, SILVANA; MONFORTE, ANNA MARIA; ROMEO, GIOVANNI; ZAPPALA, MARIA. ANNULATED 1,5
  151017. BENZODIAZEPINES. PART II. SIX MEMBERED RINGS.  HETEROCYCLES 1993, 36(4), 865
  151018. 90. A REVIEWa
  151019. GABRIEL WEATHERHEAD
  151020. 7025N
  151021. 2/28/96V
  151022. CHIMIRRI, ALBA; GITTO, ROSARIA; GRASSO, SILVANA; MONFORTE, ANNA MARIA; ROMEO, GIOVANNI; ZAPPALA, MARIA. ANNULATED 1,5
  151023. BENZODIAZEPINES. PART I. THREE, FOUR, AND FIVE MEMBERED RINGS.  HETEROCYCLES 1993, 36(3), 601
  151024. 37. A REVIEWa
  151025. GABRIEL WEATHERHEAD
  151026. 7026N
  151027. 2/28/96V
  151028. LI, WEN
  151029. REN; HAN, SO
  151030. YEOP; JOULLIE, MADELEINE M. THE DETOXIN COMPLEX
  151031. A NATURALLY OCCURRING SAFENER.  HETEROCYCLES 1993, 36(2), 359
  151032. 88. A REVIEWa
  151033. GABRIEL WEATHERHEAD
  151034. 7027N
  151035. 2/28/96V
  151036. MARTIN, MICHAEL J.; DORN, LINDA J.; COOK, JAMES M.NOVEL PYRIDODIINDOLES, AZADIINDOLES, AND INDOLOPYRIDOIMIDAZOLES VIA THE FISCHER
  151037. INDOLE CYCLIZATION.  HETEROCYCLES 1993, 36(1), 157
  151038. 89. A REVIEWa
  151039. GABRIEL WEATHERHEAD
  151040. 7028N
  151041. 2/28/96V
  151042. COHN, OTTO. THE SYNTHESIS OF PYRIDINES, QUINOLINES AND OTHER RELATED SYSTEMS BY THE VILSMEIER ANDTHE REVERSE VILSMEIER METHOD.  HETEROCYCLES 1993, 35(1), 539
  151043. 57. A REVIEWa
  151044. GABRIEL WEATHERHEAD
  151045. 7029N
  151046. 2/28/96
  151047. HAIDER, NORBERT; HEINISCH, GOTTFRIED. RECENT ADVANCES IN THE CHEMISTRY OF CONDENSED PYRIDAZINES: SYNTHESIS OF BI
  151048.  AND TRICYCLIC SYSTEMS BY ANNELATION OF FIVE
  151049. , SIX
  151050. , AND SEVEN
  151051. MEMBERED RINGS TO A PREFORMED 1,2
  151052. DIAZINENUCLEUS.  HETEROCYCLES 1993, 35(1), 519
  151053. 38. A REVIEW
  151054. GABRIEL WEATHERHEAD
  151055. 7030N
  151056. 2/28/96V
  151057. KATRITZKY, ALAN R.; GORDEEV, MIKHAIL F. HETEROCYCLIC REARRANGEMENTS OF BENZOFUROXANS AND RELATED COMPOUNDS.  HETEROCYCLES 1993, 35(1), 483
  151058. 518. A REVIEWa
  151059. GABRIEL WEATHERHEAD
  151060. 7031N
  151061. 2/28/96V
  151062. YANADA, REIKO; HARAYAMA, TAKASHI; YONEDA, FUMIO. CHEMISTRY ON THE DAMAGE AND REPAIR OF THYMINE AND THYMIDINE DERIVATIVES.  HETEROCYCLES 1993, 35(1), 461
  151063. 81. A REVIEWa
  151064. GABRIEL WEATHERHEAD
  151065. 7032N
  151066. 2/28/96V
  151067. BAUDLER, MARIANNE; GLINKA, KLAUS. CONTRIBUTIONS TO THE CHEMISTRY OF PHOSPHORUS. 218. MONOCYCLIC AND POLYCYCLIC PHOSPHINES.  CHEMICAL REVIEWS 1993, 93(4),1623
  151068. 67. A REVIEWa
  151069. GABRIEL WEATHERHEAD
  151070. 7033N
  151071. 2/28/96V
  151072. SANDER, WOLFRAM; BUCHER, GOETZ; WIERLACHER, STEFAN. CARBENES IN MATRIXES: SPECTROSCOPY, STRUCTURE, AND REACTIVITY.  CHEMICAL REVIEWS 1993, 93(4),1583
  151073. 621. A REVIEWa
  151074. GABRIEL WEATHERHEAD
  151075. 7034N
  151076. 2/28/96V
  151077. COLLINS, PAUL W.; DJURIC, STEVAN W. SYNTHESIS OF THERAPEUTICALLY USEFUL PROSTAGLANDIN AND PROSTACYCLIN ANALOGS.  CHEMICAL REVIEWS 1993, 93(4),1533
  151078. 64. A REVIEWa
  151079. GABRIEL WEATHERHEAD
  151080. 7035N
  151081. 2/28/96V
  151082. TOSHIMA, KAZUNOBU; TATSUTA, KUNIAKI. RECENT PROGRESS IN O
  151083. GLYCOSYLATION METHODS AND ITS APPLICATION TO NATURAL PRODUCTS SYNTHESIS.  CHEMICAL REVIEWS 1993, 93(4),1503
  151084. 31. A REVIEWa
  151085. GABRIEL WEATHERHEAD
  151086. 7036N
  151087. 2/28/96
  151088. VROTERA, JUNZO. TRANSESTERIFICATION.  CHEMICAL REVIEWS 1993, 93(4),1449
  151089. 70. A REVIEWa
  151090. GABRIEL WEATHERHEAD
  151091. 7037N
  151092. 2/28/96V
  151093. CHUIT, CLAUDE; CORRIU, ROBERTJ. P.; REYE, CATHERINE; YOUNG. J. COLIN. REACTIVITY OF PENTA
  151094.  AND HEXACOORDINATE SILICON COMPOUNDS AND THEIR ROLE AS REACTION INTERMEDIATES.  CHEMICAL REVIEWS 1993,93(4),1371
  151095. 448. A REVIEWa
  151096. GABRIEL WEATHERHEAD
  151097. 7038N
  151098. 2/28/96V
  151099. HOVEYDA, AMIR H.; EVANS, DAVID A.; FU, GREGORY C. SUBSTRATE
  151100. DIRECTABLE CHEMICAL REACTIONS.  CHEMICAL REVIEWS 1993, 93(4),1307
  151101. 70. A REVIEWa
  151102. GABRIEL WEATHERHEAD
  151103. 7039N
  151104. 2/28/96V
  151105. FEHLHAMMER, WOLF P.; FRITZ, MARCUS. EMERGENCE OF A CNH AND CYANO COMPLEX BASED ORGANOMETALLIC CHEMISTRY.  CHEMICAL REVIEWS 1993, 93(3),1243
  151106. 80. A REVIEWa
  151107. GABRIEL WEATHERHEAD
  151108. 7040N
  151109. 2/28/96
  151110. SAXENA, ANIL K.; HOSMANE, NARAYAN S. RECENT ADVANCES IN THE CHEMISTRY OF CARBORANE METAL COMPLEXES INCORPORATING D
  151111.  AND F
  151112. BLOCK ELEMENTS.  CHEMICAL REVIEWS 1993, 93(3),1081
  151113. 124. A REVIEWa
  151114. GABRIEL WEATHERHEAD
  151115. 7041N
  151116. 2/28/96V
  151117. HANUSA, TIMOTHY P. LIGAND INFLUENCES ON STRUCTURE AND REACTIVITY IN ORGANOALKALINE EARTH CHEMISTRY.  CHEMICAL REVIEWS 1993, 93(3),1023
  151118. 36. A REVIEWa
  151119. GABRIEL WEATHERHEAD
  151120. 7042N
  151121. 2/28/96V^SUTTON, DEREK. ORGANOMETALLIC DIAZO COMPOUNDS.  CHEMICAL REVIEWS 1993,93(3),995
  151122. 1022. A REVIEWa
  151123. GABRIEL WEATHERHEAD
  151124. 7043N
  151125. 2/28/96V}STRAUSS, STEVEN H. THE SEARCH FOR LARGER AND MORE WEAKLY COORDINATING ANIONS.  CHEMICAL REVIEWS 1993, 93(3), 927
  151126. 42. A REVIEWa
  151127. GABRIEL WEATHERHEAD
  151128. 7044N
  151129. 2/28/96V|HEINEKEY, D. M.; OLDHAM, WARREN J. JR. COORDINATION CHEMISTRY OF DIHYDROGEN.  CHEMICAL REVIEWS 1993, 93(3), 913
  151130. 26. A REVIEWa
  151131. GABRIEL WEATHERHEAD
  151132. 7045N
  151133. 2/28/96
  151134. PARKIN, GERARD. BOND
  151135. STRETCH ISOMERISM IN TRANSITION METAL COMPLEXES: A REEVALUATION OF CRYSTALLOGRAPHIC DATA.  CHEMICAL REVIEWS 1993, 93(3), 887
  151136. 911. A REVIEWa
  151137. GABRIEL WEATHERHEAD
  151138. 7046N
  151139. 2/28/96VnWINTERFELDT, EKKEHARD. ENANTIOMERICALLY PURE CYCLOPENTADIENES.  CHEMICAL REVIEWS 1993, 93(2), 827
  151140. 43. A REVIEWa
  151141. GABRIEL WEATHERHEAD
  151142. 7047N
  151143. 2/28/96V
  151144. LISSI, E. A.; ENCINAS, M. V.; LEMP, E.; RUBIO, M. A. SINGLET OXYGEN 02(1G) BIMOLECULAR PROCESSES. SOLVENT AND COMPARTMENTALIZATION EFFECTS.  CHEMICAL REVIEWS 1993, 93(2), 699
  151145. 723. A REVIEWa
  151146. GABRIEL WEATHERHEAD
  151147. 7048N
  151148. 2/28/96V
  151149. KAUPP, GERD; HAAK, MICHAEL. ABSOLUTE ASYMMETRIC SYNTHESIS BY IRRADIATION OF CHIRAL CRYSTALS.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(5), 694
  151150. 95. A REVIEWa
  151151. GABRIEL WEATHERHEAD
  151152. 7049N
  151153. 2/28/96
  151154. REISER, OLIVER. PALLADIUM
  151155. CATALYZED,ENANTIOSELECTIVE ALLYLIC SUBSTITUTION.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(4), 547
  151156. 49. A REVIEWa
  151157. GABRIEL WEATHERHEAD
  151158. 7050N
  151159. 2/28/96V
  151160. MULLER, HANS
  151161. MARTIN; SEEBACH, DIETER. POLY(HYDROXYBUTANOATES): A FIFTH CLASS OF PHYSIOLOGICALLY IMPORTANT ORGANIC BIOPOLYMERS. 1993, 32(4), 477
  151162. 502. A REVIEWa
  151163. GABRIEL WEATHERHEAD
  151164. 7051N
  151165. 2/28/96V
  151166. KESSLER, HORST. PEPTOIDS
  151167. A NEW APPROACH TO THE DEVELOPMENT OF KEY PHARMACEUTICALS.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(4), 543
  151168. 4. A REVIEWa
  151169. GABRIEL WEATHERHEAD
  151170. 7052N
  151171. 2/28/96V
  151172. KUNZ, HORST; RUCK, KAROLA. CARBOHYDRATES AS CHIRAL AUXILIARIES IN STEREOSELECTIVE SYNTHESIS.  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH 1993, 32(3), 336
  151173. 58. A REVIEWa
  151174. GABRIEL WEATHERHEAD
  151175. 7053N
  151176. 2/28/96
  151177. NECKERS, DOUGLAS C.; VALDES
  151178. AGUILERA OSCAR M. PHOTOCHEMISTRY OF THE XANTHINE DYES.  ADVANCES IN PHOTOCHEMISTRY 1993, 18, 315. A REVIEWa
  151179. GABRIEL WEATHERHEAD
  151180. 7054N
  151181. 2/28/96V
  151182. BRAUN, ANDRE M.; JAKOB, LAURENT; OLIVEROS, ESTHER; OLLER DO NASCIMENTO, CLAUDIO A. UP
  151183. SCALING PHOTOCHEMICAL REACTIONS.  ADVANCES IN PHOTOCHEMISTRY 1993,18, 235. A REVIEWa
  151184. GABRIEL WEATHERHEAD
  151185. 7055N
  151186. 2/28/96V
  151187. RAMAMURTHY, V.; WEISS, RICHARD G.; HAMMOND, GEORGE S. A MODEL FOR THE INFLUENCE OF ORGANIZED MEDIA ON PHOTOCHEMICAL REACTIONS.  ADVANCES IN PHOTOCHEMISTRY 1993,18, 67. A REVIEWa
  151188. GABRIEL WEATHERHEAD
  151189. 7056N
  151190. 2/28/96V
  151191. FRINGUELLI, FRANCESCO; MINUTI, LUCIO; PIZZO, FERDINANDO; TATICCHI, ALDO. REACTIVITY AND SELECTIVITY IN LEWIS ACID
  151192. CATALYZED DIELS
  151193. ALDER REACTIONS OF 2
  151194. CYCLOHEXENONES.  ACTA CHEMICA SCANDINAVICA 1993, 47(3), 255
  151195. 63. A REVIEWa
  151196. GABRIEL WEATHERHEAD
  151197. 7057N
  151198. 2/28/96
  151199. FUNICELLO, MARIA; SPAGNOLO, PIERO; ZANIRATO, PAOLO INTRAMOLECULAR CYCLIZATIONS AND RING
  151200. CLEAVAGE REACTIONS OF FIVE
  151201. MEMBERED HETEROARYLNITRENES AND THEIR PRECURSORS  ACTA CHEMICA SCANDINAVICA 1993, 47(3), 231
  151202. 43. A REVIEWa
  151203. GABRIEL WEATHERHEAD
  151204. 7058N
  151205. 2/28/96V
  151206. MARTIN, ARNOLD R.; YANG, YOUHUA. PALLADIUM CATALYZED CROSS
  151207. COUPLING REACTIONS OF ORGANOBORONIC ACIDS WITH ORGANIC ELECTROPHILES.  ACTA CHEMICA SCANDINAVICA 1993, 47(3), 221
  151208. 30. A REVIEWa
  151209. GABRIEL WEATHERHEAD
  151210. 7059N
  151211. 2/28/96V
  151212. UNDHEIM, KJELL; BENNECHE, TORE. METALATION AND METAL
  151213. ASSISTED BOND FORMATION IN 7R
  151214. ELECTRON DEFICIENT HETEROCYCLES.  ACTA CHEMICA SCANDINAVICA 1993, 47(2),102
  151215. 21. A REVIEWa
  151216. GABRIEL WEATHERHEAD
  151217. 7060N
  151218. 2/28/96V
  151219. WOZNIAK, MARIAN; VAN DER PLAS, HENK C. AMINATION OF NITROAZAAROMATICS.  ACTA CHEMICA SCANDINAVICA 1993, 47(2), 95
  151220. 101. A REVIEWa
  151221. GABRIEL WEATHERHEAD
  151222. 7061N
  151223. 2/28/96
  151224. GUERRIERO, PAOLO; VIGATO, PIETRO ALESSANDRO; FENTON, DAVID E.; HELLIER, PAUL C. SYNTHESIS AND APPLICATION OF MACROCYCLIC AND MACROACYCLIC SCHIFF BASES.  ACTA CHEMICA SCANDINAVICA 1992, 46(11), 1025
  151225. 46. A REVIEWa
  151226. GABRIEL WEATHERHEAD
  151227. 7062N
  151228. 2/28/96V
  151229. CHANON, MICHEL. THE VARIETY OF MOLECULAR SCHEMES AT THE BORDER BETWEEN POLAR AND ELECTRON
  151230. TRANSFER (ET) MECHANISMS.  ACTA CHEMICA SCANDINAVICA 1992, 46(8), 695
  151231. 706. A REVIEWa
  151232. GABRIEL WEATHERHEAD
  151233. 7063N
  151234. 2/28/96V
  151235. HOZ, SHMARYHAU. THE ANTI
  151236. TRADITIONAL INTERPRETATION OF THE LFER MECHANISTIC MESSAGE.  ACTA CHEMICA SCANDINAVICA 1992, 46(6), 503
  151237. 507. A REVIEWa
  151238. GABRIEL WEATHERHEAD
  151239. 7064N
  151240. 2/28/96V
  151241. BICKELHAUPT, FRIEDRICH. THE IMPORTANCE OF (INTRAMOLECULAR) SOLVATION IN ORGANOMAGNESIUM CHEMISTRY.  ACTA CHEMICA SCANDINAVICA 1992,46(5),409
  151242. 17. A REVIEWa
  151243. GABRIEL WEATHERHEAD
  151244. 7065N
  151245. 2/28/96
  151246. FAMULOK, MICHALE; NOWICK, JAMES, S.; REBEK, JR., JULIUS. SELF
  151247. REPLICATING SYSTEMS.  ACTA CHEMICA SCANDINAVICA 1992, 46(4), 315
  151248. 124. A REVIEWa
  151249. GABRIEL WEATHERHEAD
  151250. 7066N
  151251. 2/28/96V
  151252. DIEDERICH, FRANCOIS; SMITHRUD, DAVID B.; SANFORD, ELIZABETH M.; WYMAN, TARA B.; FERGUSON, STEPHEN B.; CARCANAGUE, DANIEL R.; CHAO, ITO; HOUK, K. N. SOLVENT EFFECTS IN MOLECULAR RECOGNITION. ACTA CHEMICA SCANDINAVICA 1992, 46(3), 205
  151253. 15. A REVIEWa
  151254. GABRIEL WEATHERHEAD
  151255. 7067N
  151256. 2/28/96V
  151257. IWAMURA, HIIZU; KOGA, NOBORU. STUDIES OF ORGANIC DI
  151258. , OLIGO
  151259. , AND POLYRADICALS BY MEANS OF THEIR BULK MAGNETIC PROPERTIES. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(6), 346
  151260. 51. A REVIEWa
  151261. GABRIEL WEATHERHEAD
  151262. 7068N
  151263. 2/28/96V
  151264. PFALTZ, ANDREAS. CHIRAL SEMICORRINS AND RELATED NITROGEN HETEROCYCLES AS LIGANDS IN ASYMMETRIC CATALYSIS. ACCOUNTS OF CHEMICAL RESEARCH 1993,26(6),339
  151265. 45. A REVIEWa
  151266. GABRIEL WEATHERHEAD
  151267. 7069N
  151268. 2/28/96
  151269. FIFE, THOMAS H. KINETIC AND MECHANISTIC EFFECTS OF EASE OF C
  151270. N BOND BREAKING IN AMIDE HYDROLYSIS. THE MECHANISMS OF HYDROLYSIS OF N
  151271. ACYLIMIDAZOLES AND N
  151272. ACYLBENZIMIDAZOLES. ACCOUNTS OF CHEMICAL RESEARCH 1993. 26(6). .325
  151273. 31. A REVIEWa
  151274. GABRIEL WEATHERHEAD
  151275. 7070N
  151276. 2/28/96VeGLEITER, ROLF; KRATZ, DETLEF. SUPERPHANES. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(6),311
  151277. 18. A REVIEWa
  151278. GABRIEL WEATHERHEAD
  151279. 7071N
  151280. 2/28/96V
  151281. MCADOO, DAVIDJ.; MORTON, THOMAS HELLMAN. GAS
  151282. PHASE ANALOGS OF CAGE EFFECTS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(6), 295
  151283. 302. A REVIEWa
  151284. GABRIEL WEATHERHEAD
  151285. 7072N
  151286. 2/28/96V
  151287. WAYNER, DANIAL D. M.; PARKER, VERNON D. BOND ENERGIES IN SOLUTION FROM ELECTRODE POTENTIALS AND THERMOCHEMICAL CYCLES. A SIMPLIFIED AND GENERAL APPROACH. ACCOUNTS OF CHEMICAL RESEARCH 1993,26(5),287
  151288. 94. A REVIEWa
  151289. GABRIEL WEATHERHEAD
  151290. 7073N
  151291. 2/28/96
  151292.  GRUSHIN, VLADIMIR V. REDUCTIVE ELIMINATION OF HYDROGEN CHLORIDE FROM CHLORO HYDRIDO TRANSITION METAL COMPLEXES: AN EFFICIENT AND SIMPLE METHOD FOR GENERATION OF ELECTRON
  151293. RICH, COORDINATIVELY UNSATURATED, REACTIVE IN
  151294. TERMEDIATES. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(5), 279
  151295. 86. A REVIEW
  151296. GABRIEL WEATHERHEAD
  151297. 7074N
  151298. 2/28/96V
  151299. LENGYEL, ISTVAN; EPSTEIN, IRVING R. TURING STRUCTURES IN SIMPLE CHEMICAL REACTIONS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(5), 235
  151300. 40. A REVIEWa
  151301. GABRIEL WEATHERHEAD
  151302. 7075N
  151303. 2/28/96V
  151304. COLLUM, DAVID B. SOLUTION STRUCTURES OF LITHIUM DIALKYLAMIDES AND RELATED N
  151305. LITHIATED SPECIES: RESULTS FROM 6LI
  151306. L5N DOUBLE LABELING EXPERIMENTS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(5), 227
  151307. 34. A REVIEWa
  151308. GABRIEL WEATHERHEAD
  151309. 7076N
  151310. 2/28/96
  151311. WEISSHAAR, JAMES C. BARE TRANSITION METAL ATOMS IN THE GAS PHASE: REACTIONS OF M, M+, AND M2+ WITH HYDROCARBONS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(4), 213
  151312. 19. A REVIEWa
  151313. GABRIEL WEATHERHEAD
  151314. 7077N
  151315. 2/28/96V~MENGER, FREDRIC M. ENZYME REACTIVITY FROM AN ORGANIC PERSPECTIVE. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(4), 206
  151316. 212. A REVIEWa
  151317. GABRIEL WEATHERHEAD
  151318. 7078N
  151319. 2/28/96V
  151320. LOOK, GARY C.; FOTSCH, CHRISTOPHER H.; WONG, CHI HUEY. ENZYME
  151321. CATALYZED ORGANIC SYNTHESIS: PRACTICAL ROUTES TO AZA SUGARS AND THEIR ANALOGS FOR USE AS GLYCO
  151322. PROCESSING INHIBITORS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(4),182
  151323. 90. A REVIEWa
  151324. GABRIEL WEATHERHEAD
  151325. 7079N
  151326. 2/28/96V
  151327. GUENARD, DANIEL; GUERITTE
  151328. VOEGELEIN, FRANCOISE; POTIER, PIERRE. TAXOL AND TAXOTERE: DISCOVERY, CHEMISTRY, AND STRUCTURE
  151329. ACTIVITY RELATIONSHIPS. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(4),160
  151330. 7. A REVIEWa
  151331. GABRIEL WEATHERHEAD
  151332. 7080N
  151333. 2/28/96
  151334. HANSCH, CORWIN. QUANTITATIVE STRUCTURE
  151335. ACTIVITY RELATIONSHIPS AND THE UNNAMED SCIENCE. ACCOUNTS OF CHEMICAL RESEARCH 1993, 26(4),147
  151336. 53. A REVIEWa
  151337. GABRIEL WEATHERHEAD
  151338. 7081N
  151339. 2/28/96V
  151340. IKEKAWA, NOBUO; MORISAKI, MASUO; FUJIMOTO, YOSHI
  151341. NORI. STEROL METABOLISM IN INSECTS: DEALKYLATION OF PHYTOSTEROL TO CHOLESTEROL. 1993, ACCOUNTS OF CHEMICAL RESEARCH 26(4),139
  151342. 46. A REVIEWa
  151343. GABRIEL WEATHERHEAD
  151344. SYNLETTCaRUDORF CONJUGATE ADDITION MICHAEL INTRAMOLECULAR ALKYNE BALDWIN RULE ACETYLENE NUCLEOPHILE REVIEWM
  151345. 7082N
  151346. 2/28/96VOINTRAMOLECULAR MICHAEL AND ANTI MICHAEL ADDITIONS TO CARBON
  151347. CARBON TRIPLE BONDSW
  151348. 1993 P 369a
  151349. GABRIEL WEATHERHEAD
  151350. ACC CHEM RESCoPFALTZ REVIEW CATALYST CHIRAL CYCLOPROPANE CYCLOPROPANATION DIAZO CORRIN ASYMMETRIC INDUCTION CARBENE CARBENOIDM
  151351. 7083N
  151352. 2/28/96VOCHIRAL SEMICORRINS AND NITROGEN HETEROCYCLES AS LIGANDS IN ASYMMETRIC CATALYSISW
  151353. VOL 26 1993 P 339a
  151354. GABRIEL WEATHERHEAD
  151355. ORG PREP PROCEDURE INTC
  151356. NAGAI TM
  151357. 7084N
  151358. 2/28/96VaRECENT PROGRESS IN THE PREPARATION AND SYNTHETIC USES OF THE REACTIONS OF 3H
  151359. PYRAZOLES 
  151360.  A REVIEWW
  151361. 1993 AUGX
  151362. 25(4)a
  151363. GABRIEL WEATHERHEAD
  151364. ORG PREP PROCEDURE INTC
  151365. MOTOHASHI NM
  151366. 7085N
  151367. 2/28/96V5SYNTHESIS OF CARCINOGENIC BENZ[C]ACRIDINES 
  151368.  A REVIEWW
  151369. 1993 JUNX
  151370. 25(3)a
  151371. GABRIEL WEATHERHEAD
  151372. 7086N
  151373. 2/28/96VyTRAVEN, VALERY F. FRONTIER ORBITALS AND PROPERTIES OF ORGANIC MOLECULES. ELLIS HORWOOD: CHICHESTER, U. K., 1992. A REVIEWa
  151374. GABRIEL WEATHERHEAD
  151375. 7087N
  151376. 2/28/96V
  151377. SIMPKINS, NIGEL S. SULPHONES IN ORGANIC SYNTHESIS (TETRAHEDRON ORGANIC CHEMISTRY SERIES, VOL. 10). PERGAMON: OXFORD, U. K., 1993. A REVIEWa
  151378. GABRIEL WEATHERHEAD
  151379. 7088N
  151380. 2/28/96V
  151381. SCHWARZENBACH, RENE P.; GSCHWEND, PHILIP M.; IMBODEN, DIETER M. ENVIRONMENTAL ORGANIC CHEMISTRY. WILEY: NEW YORK, 1993. A REVIEWa
  151382. GABRIEL WEATHERHEAD
  151383. 7089N
  151384. 2/28/96
  151385. 5V|SCHEFFOLD, ROLF, ED. MODERN SYNTHETIC METHODS 1992, VOL. 6. VERLAG HELVETICA CHIMICA ACTA: BASEL SWITZERLAND, 1992. A REVIEWa
  151386. GABRIEL WEATHERHEAD
  151387. 7090N
  151388. 2/28/96ViPOPPE, L.; NOVAK, L. SELECTIVE BIOCATALYSIS. A SYNTHETIC APPROACH. VCH: WEINHEIM, GERMANY, 1992. A REVIEWa
  151389. GABRIEL WEATHERHEAD
  151390. 7091N
  151391. 2/28/96VPPATONAY, GABOR, ED. HPLC DETECTION. NEWER METHODS. VCH: NEW YORK, 1992. A REVIEWa
  151392. GABRIEL WEATHERHEAD
  151393. 7092N
  151394. 2/28/96V
  151395. MCLAFFERTY, FRED W.; TURECEK, FRANTISEK. INTERPRETATION OF MASS SPECTRA, 4TH ED. UNIVERSITY SCIENCE BOOKS: MILL VALLEY, CA, 1993. A REVIEWa
  151396. GABRIEL WEATHERHEAD
  151397. 7093N
  151398. 2/28/96V
  151399. MAYO, D. W.; PIKE, R. M.; BUTCHER, S. S.; TRUMPER, P. K. MICROSCALE TECHNIQUES FOR THE ORGANIC LABORATORY. WILEY: NEW YORK, 1991. A REVIEWa
  151400. GABRIEL WEATHERHEAD
  151401. 7094N
  151402. 2/28/96
  151403. :VjMARCINIEC, BOGDAN, ED. COMPREHENSIVE HANDBOOK OF HYDRO SILYLATION. PERGAMON: OXFORD, U. K., 1992. A REVIEWa
  151404. GABRIEL WEATHERHEAD
  151405. 7095N
  151406. 2/28/96VtMALKIN, JACOB. PHOTOPHYSICAL AND PHOTOCHEMICAL PROPERTIES OF AROMATIC COMPOUNDS. CRC: BOCA RATON, FL, 1992. A REVIEWa
  151407. GABRIEL WEATHERHEAD
  151408. 7096N
  151409. 2/28/96V
  151410. JONES, R. ALAN, ED. PYRROLES. PART 2. THE SYNTHESIS, REACTIVITY, AND PHYSICAL PROPERTIES OF SUBSTITUTED PYRROLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 48, PART 2). WILEY: NEW YORK, 1992. A REVIEWa
  151411. GABRIEL WEATHERHEAD
  151412. 7097N
  151413. 2/28/96V
  151414. IZUMI, YUSUKE; URABE, KAZUO; ONAKA, MAKOTO. ZEOLITE, CLAY, AND HETEROPOLY ACID IN ORGANIC REACTIONS. VCH: NEW YORK AND KODANSHA LTD.: TOKYO, JAPAN, 1992. A REVIEWa
  151415. GABRIEL WEATHERHEAD
  151416. 7098N
  151417. 2/28/96V\HO, TSE
  151418. LOK. HETEROLYTIC FRAGMENTATION OF ORGANIC MOLECULES. WILEY: NEW YORK, 1993. A REVIEWa
  151419. GABRIEL WEATHERHEAD
  151420. 7099N
  151421. 2/28/96
  151422. HERMECZ, ISTVAN; KERESZTURI, GEZA; VASVARI
  151423. DEBRECZY, LELLE. AMINOMETHYLENEMALONATES AND THEIR USE IN HETEROCYCLIC SYNTHESIS (ADVANCES IN HETEROCYCLIC CHEMISTRY, VOL. 54). ACADEMIC: SAN DIEGO, CA, 1992. A REVIEWa
  151424. GABRIEL WEATHERHEAD
  151425. 7100N
  151426. 2/28/96V
  151427. HERBST, WILLY; HUNGER, KLAUS. INDUSTRIAL ORGANIC PIGMENTS. PRODUCTION, PROPERTIES, APPLICATIONS. VCH: WEINHEIM, GERMANY, 1993. A REVIEWa
  151428. GABRIEL WEATHERHEAD
  151429. 7101N
  151430. 2/28/96V
  151431. HEILBRONNER, EDGAR; DUNITZ, JACK D. REFLECTIONS ON SYMMETRY IN CHEMISTRY.... AND ELSEWHERE. VERLAG HELVETICA CHIMICA ACTA: BASEL, SWITZERLAND, 1993. A REVIEWa
  151432. GABRIEL WEATHERHEAD
  151433. 7102N
  151434. 2/28/96V
  151435. HALGAS, JAN. BIOCATALYSTS IN ORGANIC SYNTHESIS (STUDIES IN ORGANIC CHEMISTRY. 46). ELSEVIER: AMSTERDAM, NETHERLANDS, 1992. A REVIEWa
  151436. GABRIEL WEATHERHEAD
  151437. 7103N
  151438. 2/28/96
  151439. GOMEZ
  151440. PUYOUG, ARMANDO; DARSZON, ALBERTO; TUENA DE GOMEZ
  151441. PUYOUG, MARIETTA, EDS. BIOMOLECULES IN ORGANIC SOLVENTS. CRC PRESS: BOCA RATON, FL, 1992. A REVIEWa
  151442. GABRIEL WEATHERHEAD
  151443. 7104N
  151444. 2/28/96VRGEORG, GUNDA I., ED. ORGANIC CHEMISTRY OF 
  151445. LACTAMS. VCH: NEW YORK, 1992. A REVIEWa
  151446. GABRIEL WEATHERHEAD
  151447. 7105N
  151448. 2/28/96VcCOOPER, STEPHEN, R., ED. CROWN COMPOUNDS: TOWARD FUTURE APPLICATIONS. VCH: NEW YORK, 1992. A REVIEWa
  151449. GABRIEL WEATHERHEAD
  151450. 7106N
  151451. 2/28/96V
  151452. COLLINS, A. N.; SHELDRAKE, G. N.; CROSBY, J., EDS. CHIRALITY IN INDUSTRY: THE COMMERCIAL MANUFACTURE AND APPLICATIONS OF OPTICALLY ACTIVE COMPOUNDS. WILEY: NEW YORK, 1993. A REVIEWa
  151453. GABRIEL WEATHERHEAD
  151454. 7107N
  151455. 2/28/96V
  151456. BUNCEL, E.; SAUNDERS, W. H., JR., EDS. ISOTOPES IN ORGANIC CHEMISTRY, VOL. 8: HEAVY ATOM ISOTOPE EFFECTS. ELSEVIER: AMSTERDAM, NETHERLANDS, 1992. A REVIEWa
  151457. GABRIEL WEATHERHEAD
  151458. 7108N
  151459. 2/28/96
  151460. BREITMAIER, E. STRUCTURE ELUCIDATION BY NMR IN ORGANIC CHEMISTRY (TRANSLATED BY JULIA WADE). WILEY: CHICHESTER, U. K., 1993. A REVIEWa
  151461. GABRIEL WEATHERHEAD
  151462. 7109N
  151463. 2/28/96VcBIDLINGMEYER, BRIAN A. PRACTICAL HPLC METHODOLOGY AND APPLICATIONS. WILEY: NEW YORK, 1992. A REVIEWa
  151464. GABRIEL WEATHERHEAD
  151465. 7110N
  151466. 2/28/96VgBALOGH, M.; LASZLO, P. ORGANIC CHEMISTRY USING CLAYS. SPRINGER
  151467.  VERLAG: BERLIN, GERMANY, 1993. A REVIEWa
  151468. GABRIEL WEATHERHEAD
  151469. 7111N
  151470. 2/28/96V
  151471. MORI, MIWAKO. SYNTHESES OF SOME NATURAL PRODUCTS USING ZIRCONIUM
  151472. PROMOTED REDUCTIVE CYCLIZATION, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151473. GABRIEL WEATHERHEAD
  151474. 7112N
  151475. 2/28/96V
  151476. MALETINA, I. I.; MIRONOVA, A. A.; ORDA, V. V.; YAGUPOLSKII, L. M. ARYLPERFLUOROALKYL
  151477.  AND ARYLPOLYFLUOROALKYLIODONIUM SALTS, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151478. GABRIEL WEATHERHEAD
  151479. 7113N
  151480. 2/28/96
  151481. SAWADA, HIDEO. FLUORINATED ORGANIC PEROXIDES
  151482.  THEIR DECOMPOSITION BEHAVIOR AND APPLICATIONS, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151483. GABRIEL WEATHERHEAD
  151484. 7114N
  151485. 2/28/96V
  151486. OKAMOTO, YOSHIKI; TAKAMUKU, SETSUO. PHOTOCHEMICAL C
  151487. P BOND CLEAVAGE OF ALKYLPHOSPHONIC ACID, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151488. GABRIEL WEATHERHEAD
  151489. 7115N
  151490. 2/28/96V
  151491. TROEV, KOLJO. DIALKYL HYDROGEN PHOSPHONATES 1. STRUCTURES OF DIALKYL HYDROGEN PHOSPHONATES, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151492. GABRIEL WEATHERHEAD
  151493. 7116N
  151494. 2/28/96V
  151495. BARANIAK, JANINA; STEC, WOJCIECH J. STEREOCONTROLLED SYNTHESES OF P
  151496. CHIRAL ANALOGUES OF NUCLEOSIDE CYCLIC 3',5'
  151497. PHOSPHATES, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151498. GABRIEL WEATHERHEAD
  151499. 7117N
  151500. 2/28/96
  151501. KUDO, TAKAKO; NAGASE, SHIGERU. CATIONS OF STRAINED POLYCYCLIC COMPOUNDS WITH SI, GE, SN, AND PB SKELETONS: THEORETICAL STUDY OF STRUCTURES AND PROPERTIES, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151502. GABRIEL WEATHERHEAD
  151503. 7118N
  151504. 2/28/96V
  151505. YOSHIDA, MASATO. UTILITY OF HIGHLY ELECTROPHILIC PEROXIDES FOR FUNCTIONALIZATIONS OF AROMATIC RINGS, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151506. GABRIEL WEATHERHEAD
  151507. 7119N
  151508. 2/28/96V`CHOU, TA
  151509. SHUE. HETEROAROMATIC ORTHO
  151510. QUINODIMETHANES, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151511. GABRIEL WEATHERHEAD
  151512. 7120N
  151513. 2/28/96V
  151514. EIKI, TOSHIO; TAGAKI, WAICHIRO. METAL ION EFFECTS IN THE REACTIONS OF PHOSPHOSULFATES, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151515. GABRIEL WEATHERHEAD
  151516. 7121N
  151517. 2/28/96
  151518. TOKUNO, KENJI; MIYOSHI, FUMIHISA; TSUTOMU, OHASHI. APPLICATIONS OF SOLID
  151519. STATE REACTIONS FOR ALKYLATION, ESTERIFICATION AND OTHER RELATED REACTIONS, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151520. GABRIEL WEATHERHEAD
  151521. 7122N
  151522. 2/28/96V
  151523. VALLEE, YANNICK. APPLICATIONS OF FLASH VACUUM THERMOLYSIS TO THE SYNTHESIS OF REACTIVE THIOCARBONYL COMPOUNDS, REVIEW ON HETEROATOM CHEM. VOL. 8. A REVIEWa
  151524. GABRIEL WEATHERHEAD
  151525. 7123N
  151526. 2/28/96
  151527. HLADKA, EVA; KOCA, JAROSLAV; KRATOCHVLL, MILAN; KVASNICKA, VLADIMIR; MATYSKA, LUDEK; POSPICHAL, JIRI; POTUCEK, VLADIMIR. THE SYNTHON MODEL AND THE PROGRAM PEGAS FOR COMPUTER ASSISTED ORGANIC SYNTHESIS. 1993, 166 (ORGANIC PEROXYGEN CHEMISTRY), 121
  151528. 197 TOPICS IN CURRENT CHEM. A REVIEW
  151529. GABRIEL WEATHERHEAD
  151530. 7124N
  151531. 2/28/96
  151532. CYVIN, SVEN J.; CYVIN, BJORG N.; BRUNVOLL, JON. ENUMERATION OF BENZENOID CHEMICAL ISOMERS WITH A STUDY OF CONSTANT
  151533. ISOMER SERIES. 1993,166 (ORGANIC PEROXYGEN CHEMISTRY), 65
  151534. 119 TOPICS IN CURRENT CHEM. A REVIEWa
  151535. GABRIEL WEATHERHEAD
  151536. 7125N
  151537. 2/28/96V
  151538. CARLSON, ROLF; NORDAHL, AKE. EXPLORING ORGANIC SYNTHETIC EXPERIMENTAL PROCEDURES. 1993,166 (ORGANIC PEROXYGEN CHEMISTRY), 1
  151539. 64 TOPICS IN CURRENT CHEM. A REVIEWa
  151540. GABRIEL WEATHERHEAD
  151541. 7126N
  151542. 2/28/96V
  151543. DEAR, K. M. CLEANING
  151544. UP OXIDATIONS WITH HYDROGEN PEROXIDE. 1993,164 (COMPUTER CHEMISTRY), 115
  151545. 125 TOPICS IN CURRENT CHEM. A REVIEWa
  151546. GABRIEL WEATHERHEAD
  151547. 7127N
  151548. 2/28/96V
  151549. FOSSEY, JACQUES; LEFORT, DANIEL; SORBA, JANINE. PERACIDS AND FREE RADICALS: A THEORETICAL AND EXPERIMENTAL APPROACH. 1993,164 (COMPUTER CHEMISTRY), 99
  151550. 113 TOPICS IN CURRENT CHEM. A REVIEWa
  151551. GABRIEL WEATHERHEAD
  151552. 7128N
  151553. 2/28/96
  151554. WARWEL, SIEGFRIED; SOJKA, MICHAEL; RUSCH GEN. KLAAS, MARK. SYNTHESIS OF DICARBOXYLIC ACIDS BY TRANSITION
  151555. METAL CATALYZED OXIDATIVE CLEAVAGE OF TERMINAL
  151556. UNSATURATED FATTY ACIDS. 1993,164 (COMPUTER CHEMISTRY), 79
  151557. 98 TOPICS IN CURRENT CHEM. A REVIEWa
  151558. GABRIEL WEATHERHEAD
  151559. 7129N
  151560. 2/28/96V
  151561. HOFT, EUGEN. ENANTIOSELECTIVE EPOXIDATION WITH PEROXIDIC OXYGEN. 1993,164 (COMPUTER CHEMISTRY), 63
  151562. 77 TOPICS IN CURRENT CHEM. A REVIEWa
  151563. GABRIEL WEATHERHEAD
  151564. 7130N
  151565. 2/28/96V
  151566. ADAM, WALDEMAR; HADJIARAPOGLOU, LAZAROS. DIOXIRANES: OXIDATION CHEMISTRY MADE EASY. 1993,164 (COMPUTER CHEMISTRY), 45
  151567. 62 TOPICS IN CURRENT CHEM. A REVIEWa
  151568. GABRIEL WEATHERHEAD
  151569. 7131N
  151570. 2/28/96V
  151571. SHELDON, R. A. HOMOGENEOUS AND HETEROGENEOUS CATALYTIC OXIDATIONS WITH PEROXIDE REAGENTS. 1993,164 (COMPUTER CHEMISTRY), 21
  151572. 43 TOPICS IN CURRENT CHEM. A REVIEWa
  151573. GABRIEL WEATHERHEAD
  151574. 7132N
  151575. 2/28/96
  151576. HEANEY, HARRY. NOVEL ORGANIC PEROXYGEN REAGENTS FOR USE IN ORGANIC SYNTHESIS. 1993,164 (COMPUTER CHEMISTRY), 1
  151577. 19 TOPICS IN CURRENT CHEM. A REVIEWa
  151578. GABRIEL WEATHERHEAD
  151579. 7133N
  151580. 2/28/96V
  151581. WALLBAUM, SABINE; MARTENS, JURGEN. ASYMMETRIC SYNTHESES WITH CHIRAL OXAZABOROLIDINES. 1992, 3(12),1475
  151582. 504 TETRAHEDRON: ASYMMETRY. A REVIEWa
  151583. GABRIEL WEATHERHEAD
  151584. 7134N
  151585. 2/28/96V
  151586. LOHRAY, BRAJ B. RECENT ADVANCES IN THE ASYMMETRIC DIHYDROXYLATION OF ALKENES. 1992, 3(11),1317
  151587. 49 TETRAHEDRON: ASYMMETRY. A REVIEWa
  151588. GABRIEL WEATHERHEAD
  151589. 7135N
  151590. 2/28/96V~NEWCOMB, MARTIN. COMPETITION METHODS AND SCALES FOR ALKYL
  151591.  RADICAL REACTION KINETICS. 1993,49(6),1151
  151592. 76 TETRAHEDRON. A REVIEWa
  151593. GABRIEL WEATHERHEAD
  151594. 7136N
  151595. 2/28/96V
  151596. KIM, BYEANG HYEAN; CURRAN, DENNIS P. ASYMMETRIC THERMAL REACTIONS WITH OPPOLZER'S CAMPHOR SULTAM. 1993, 49(2), 293
  151597. 318 TETRAHEDRON. A REVIEWa
  151598. GABRIEL WEATHERHEAD
  151599. 7137N
  151600. 2/28/96
  151601. eV^BALZANI, VINCENZO. SUPRAMOLECULAR PHOTOCHEMISTRY. 1992, 48(48),10443
  151602. 514 TETRAHEDRON. A REVIEWa
  151603. GABRIEL WEATHERHEAD
  151604. 7138N
  151605. 2/28/96V
  151606. AFARINKIA, KAMYAR; VINADER, VICTORIA; NELSON, TODD D.; POSNER, GARY H. DIELS
  151607. ALDER CYCLOADDITIONS OF 2
  151608. PYRONES AND 2
  151609. PYRIDONES. 1992, 48(42), 9111
  151610. 71 TETRAHEDRON. A REVIEWa
  151611. GABRIEL WEATHERHEAD
  151612. 7139N
  151613. 2/28/96V
  151614. MUZART, JACQUES. SILYL ETHERS AS PROTECTIVE GROUPS FOR ALCOHOLS: OXIDATIVE DEPROTECTION AND STABILITY UNDER ALCOHOL OXIDATION CONDITIONS. 1993, (1),11
  151615. 27 SYNTHESIS. A REVIEWa
  151616. GABRIEL WEATHERHEAD
  151617. 7140N
  151618. 2/28/96V
  151619. LEMMEN, P.; RICHTER, W.; WERNER, B.; KARL, R.; STUMPF, R.; UGI, I. FIVE
  151620.  MEMBERED CYCLIC PHOSPHORYLATING REAGENTS AND RELATED COMPOUNDS. 1993, (1),1
  151621. 10 SYNTHESIS. A REVIEWa
  151622. GABRIEL WEATHERHEAD
  151623. 7141N
  151624. 2/28/96V
  151625. METZNER, PATRICK. THE USE OF THIOCARBONYL COMPOUNDS IN CARBON
  151626. CARBON BOND FORMING REACTIONS. 1992, (12), 1185
  151627. 1199 SYNTHESIS. A REVIEW
  151628. GABRIEL WEATHERHEAD
  151629. 7142N
  151630. 2/28/96VrLOHRAY, BRAJ B. CYCLIC SULFITES AND CYCLIC SULFATES: EPOXIDE LIKE SYNTHONS. 1992, (11),1035
  151631. 52 SYNTHESIS. A REVIEWa
  151632. GABRIEL WEATHERHEAD
  151633. 7143N
  151634. 2/28/96V
  151635. BROWN, ROGER F. C.; EASTWOOD, FRANK W. GAS PHASE CHEMISTRY OF KETENES, CARBENES, ACETYLENES AND ARYNES: SYNTHETIC CONSEQUENCES. 1993, (1), 9
  151636. 19 SYNLETT. A REVIEWa
  151637. GABRIEL WEATHERHEAD
  151638. 7144N
  151639. 2/28/96V
  151640. BRANDI, ALBERTO; CORDERO, FRANCA M.; DE SARLO, FRANCESCO; GOTI, ANDREA; GUARNA, ANTONIO. NEW SYNTHESIS OF AZAHETEROCYCLES BY REARRANGEMENT OF ISOXAZOLINE
  151641. SPIROCYCLOALKANE COMPOUNDS. 1993, (1),1
  151642. 8 SYNLETT. A REVIEWa
  151643. GABRIEL WEATHERHEAD
  151644. 7145N
  151645. 2/28/96V
  151646. CURRAN, DENNIS P.; FEVIG, THOMAS L.; JASPERSE, CRAIG P.; TOTLEBEN, MICHAEL J. NEW MECHANISTIC INSIGHTS INTO REDUCTIONS OF HALIDES AND RADICALS WITH SAMARIUM(II) IODIDE. 1992, (12), 943
  151647. 61 SYNLETT. A REVIEWa
  151648. GABRIEL WEATHERHEAD
  151649. 2/28/96
  151650. FRASER
  151651. REID, BERT; UDODONG, UKO E.; WU, ZUFAN; OTTOSSON, HAKAN; MERRITT, J. ROBERT; RAO, C. SRINIVAS; ROBERTS, CARMICHAEL; MADSEN, ROBERT. N
  151652. PENTENYL GLYCOSIDES IN ORGANIC CHEMISTRY: A CONTEMPORARY EXAMPLE OF SERENDIPITY. 1992, (12), 927
  151653. 42 SYNLETT. A REVIEW
  151654. GABRIEL WEATHERHEAD
  151655. 7147N
  151656. 2/28/96VtZECCHI, GAETANO. CHEMISTRY OF C
  151657. AZIDOHYDRAZONES: DEVELOPMENTS AND PERSPECTIVES. 1992, (11), 858
  151658. 60 SYNLETT. A REVIEWa
  151659. GABRIEL WEATHERHEAD
  151660. 7148N
  151661. 2/28/96V
  151662. SATO, FUMIE; KOBAYASHI, YUICHI. SYNTHESIS OF ENANTIOMERICALLY PURE SECONDARY 
  151663. HALO ALLYLIC ALCOHOLS AND THEIR USE IN THE SYNTHESIS OF LEUKOTRIENES. 1992, (11), 849
  151664. 57 SYNLETT. A REVIEWa
  151665. GABRIEL WEATHERHEAD
  151666. 7149N
  151667. 2/28/96V
  151668. RESHETOVA, I. G.; TKHAPER, R. K.; KAMERNITSKII, A. V. PROGRESS IN THE FIELD OF PHYSIOLOGICALLY ACTIVE LANOSTEROL COMPOUNDS. 1992, 61(8), 859 RUSSIAN CHEM. REV. A REVIEWa
  151669. GABRIEL WEATHERHEAD
  151670. 7150N
  151671. 2/28/96
  151672. KRYLOV, O. V. METHODS FOR INCREASING THE EFFICIENCY OF CATALYSIS FOR THE OXIDATIVE CONDENSATION OF METHANE. 1992, 61(8), 851 RUSSIAN CHEM. REV. A REVIEWa
  151673. GABRIEL WEATHERHEAD
  151674. 7151N
  151675. 2/28/96VyOSIPOV, S. N.; KOLOMIETS, A. F.; FOKIN, A. V. FLUORINE
  151676. CONTAINING KETIMINES. 1992, 61(8), 798 RUSSIAN CHEM. REV. A REVIEWa
  151677. GABRIEL WEATHERHEAD
  151678. 7152N
  151679. 2/28/96V
  151680. GOLUBEV, A. S.; KOLOMIETS, A. F.; FOKIN, A. V. REACTIONS OF POLYFLUORO KETONES WITH UNSATURATED COMPOUNDS. 1992, 61(8), 779 RUSSIAN CHEM. REV. A REVIEWa
  151681. GABRIEL WEATHERHEAD
  151682. 7153N
  151683. 2/28/96V
  151684. FOKIN, A. V.; TYUTIN, V. YU.; CHKANIKOV, N. D. THE CHEMISTRY OF PERFLUOROALKYL
  151685. SUBSTITUTED DICYANOETHYLENES. 1992, 61(8), 766 RUSSIAN CHEM. REV. A REVIEWa
  151686. GABRIEL WEATHERHEAD
  151687. 7154N
  151688. 2/28/96
  151689. ODINOKOV, V. N.; KUKOVINETS, O. S.; ZAINULLIN, R. A.; TOLSTIKOV, G. A. THE SYNTHESIS OF INSECT JUVENILE HORMONES AND THEIR ANALOGUES. 1992, 61(7), 731 RUSSIAN CHEM. REV. A REVIEWa
  151690. GABRIEL WEATHERHEAD
  151691. 7155N
  151692. 2/28/96VzVLAD, P. F.; ARYKU, A. N. OZONOLYTIC TRANSFORMATIONS OF LABDANE DITERPENOIDS. 1992, 61(7), 716 RUSSIAN CHEM. REV. A REVIEWa
  151693. GABRIEL WEATHERHEAD
  151694. 7156N
  151695. 2/28/96V
  151696. BARABANOV, V. G.; GOLOVIN, A. V.; RODIN, A. A.; USTENKO, A. A. THE ELECTRONIC STRUCTURE AND REACTIVITY OF ALKENES. 1992, 61(7), 697 RUSSIAN CHEM. REV. A REVIEWa
  151697. GABRIEL WEATHERHEAD
  151698. 7157N
  151699. 2/28/96VnKUZNETSOVA, N. A.; KALIYA, O. L. THE PHOTOCHEMISTRY OF COUMARINS. 1992, 61(7), 683 RUSSIAN CHEM. REV. A REVIEWa
  151700. GABRIEL WEATHERHEAD
  151701. 7158N
  151702. 2/28/96V
  151703. BASILEVSKII, M. V.; FAUSTOV, V. I. MODERN THEORIES OF CHEMICAL REACTIONS IN CONDENSED PHASES. 1992, 61(7), 651 RUSSIAN CHEM. REV. A REVIEWa
  151704. GABRIEL WEATHERHEAD
  151705. 7159N
  151706. 2/28/96V
  151707. EGOROCHKIN, A. N. CONJUNCTION (SIC) IN ORGANIC COMPOUNDS OF SILICON
  151708. SUBGROUP ELEMENTS. 1992, 61(6), 600 RUSSIAN CHEM. REV. A REVIEWa
  151709. GABRIEL WEATHERHEAD
  151710. 7160N
  151711. 2/28/96V
  151712. SIMONOVA, T. P.; NEFEDOV, V. D.; TOROPOVA, M. A.; KIRILLOV, N. F. CURRENT APPROACH TO THE PROBLEM OF NITRENIUM IONS. 1992, 61(6), 584 RUSSIAN CHEM. REV. A REVIEWa
  151713. GABRIEL WEATHERHEAD
  151714. 7161N
  151715. 2/28/96V
  151716. ZHDANOV, YU A.; ALEKSEEV, YU E.; KOMPANTSEVA, E. V.; VERGEYCHIK, E. N. INDUCED OPTICAL ACTIVITY IN CYCLODEXTRIN COMPLEXES. 1992, 61(6), 563 RUSSIAN CHEM. REV. A REVIEWa
  151717. GABRIEL WEATHERHEAD
  151718. 7162N
  151719. 2/28/96V
  151720. ROUSSEL, CHRISTIAN; PIRAS, PATRICK. CHIRBASE: A MOLECULAR DATABASE FOR STORAGE AND RETRIEVAL OF CHROMATOGRAPHIC CHIRAL SEPARATIONS. 1993, 65(2), 235
  151721. 44 PURE AND APPLIED CHEM. A REVIEWa
  151722. GABRIEL WEATHERHEAD
  151723. 7163N
  151724. 2/28/96
  151725. TAKAHASHI, KAZUKO. CONJUGATION
  151726. EXTENDED RING ASSEMBLIES WITH CENTRAL HETEROCYCLES. NEW MULTISTAGE REDOX SYSTEMS. 1993, 65(1), 127
  151727. 34 PURE AND APPLIED CHEM. A REVIEWa
  151728. GABRIEL WEATHERHEAD
  151729. 7164N
  151730. 2/28/96VhPASCAL, ROBERT A., JR. TORMENTED AROMATIC COMPOUNDS. 1993, 65(1), 105
  151731. 10 PURE AND APPLIED CHEM. A REVIEWa
  151732. GABRIEL WEATHERHEAD
  151733. 7165N
  151734. 2/28/96V
  151735. KOMATSU, KOICHI. THE CHEMISTRY OF CYCLIC 
  151736. SYSTEMS SURROUNDED BY RIGID 
  151737. FRAMEWORKS: BLENDING A 
  151738. FLAVOR INTO THE AROMATICS. 1993, 65(1), 73
  151739. 80. A REVIEWa
  151740. GABRIEL WEATHERHEAD
  151741. 7166N
  151742. 2/28/96V
  151743. GINGRICH, HENRY L.; GHOSH, TIRTHANKAR; HUANG, QIURONG; LI, JI; JONES, MAITLAND, JR. CARBORANYLCARBENES AND DEHYDROCARBORANES. 1993, 65(1), 65
  151744. 71 PURE AND APPLIED CHEM. A REVIEWa
  151745. GABRIEL WEATHERHEAD
  151746. 7167N
  151747. 2/28/96
  151748. HIBERTY, P. C.; OHANESSIAN, G.; SHAIK, S. S.; FLAMENT, J. P. THE DELOCALIZATION OF 1R ELECTRONIC SYSTEMS AS A DESTABILIZING CONSTRAINT IMPOSED BY THE A FRAME. ALLYL, BENZENE, CYCLOBUTADIENE AND RELATED HETEROANNULENES. 1993, 65(1), 35
  151749. 45 PURE AND APPLIED CHEM. A REVIEW
  151750. GABRIEL WEATHERHEAD
  151751. 7168N
  151752. 2/28/96V
  151753. BALABAN, ALEXANDRU T. BENZENOID CATAFUSENES: PERFECT MATCHINGS, ISOMERIZATION, AUTOMERIZATION. 1993, 65(1),1
  151754. 9 PURE AND APPLIED CHEM. A REVIEWa
  151755. GABRIEL WEATHERHEAD
  151756. 7169N
  151757. 2/28/96V
  151758. BHUPATHY, M.; HUGHES, D. L.; AMATO, J. S.; BERGAN, J. J.; LEAZER, J. L.; LOVELACE, T. C.; MCNAMARA, J. M.; ET AL. ENZYMES AND PRACTICAL ASYMMETRIC SYNTHESIS. 1939, 64(12),1939
  151759. 44 PURE AND APPLIED CHEM. A REVIEWa
  151760. GABRIEL WEATHERHEAD
  151761. 7170N
  151762. 2/28/96
  151763. ROBERTS, S. M. THE USE OF ENZYMES FOR THE CATALYSIS OF KEY REACTIONS IN THE SYNTHESIS OF BIOLOGICALLY ACTIVE NATURAL PRODUCTS AND ANALOGS. 1992, 64(12),1933
  151764. 7 PURE AND APPLIED CHEM. A REVIEWa
  151765. GABRIEL WEATHERHEAD
  151766. 7171N
  151767. 2/28/96V
  151768. CHARETTE, ANDRE B.; MELLON, CHRISTOPHE; ROUILLARD, LANGIS; MALENFANT, ERIC. DESIGN, SYNTHESIS, AND APPLICATIONS OF NEW OXYGENATED CHIRAL AUXILIARIES. 1992, 64(12), 1925
  151769. 31 PURE AND APPLIED CHEM. A REVIEWa
  151770. GABRIEL WEATHERHEAD
  151771. 7172N
  151772. 2/28/96V
  151773. BELOKON, YURI N. CHIRAL COMPLEXES OF NICKEL(II), COPPER(II) AND COPPER(I) AS REAGENTS, CATALYSTS AND RECEPTORS FOR ASYMMETRIC SYNTHESIS AND CHIRAL RECOGNITION OF AMINO ACIDS. 1917, 64(12),1917
  151774. 24 PURE AND APPLIED CHEM. A REVIEWa
  151775. GABRIEL WEATHERHEAD
  151776. 7173N
  151777. 2/28/96
  151778. DUTHALER, RUDOLF O.; HAFNER, ANDREAS; ALSTERS, PAUL L.; ROTHE, STREIT PETRA; RIHS, GRETY. STEREOSELECTIVE TRANSFORMATIONS MEDIATED BY CHIRAL MONOCYCLOPENTADIENYL TITANIUM, ZIRCONIUM, AND HAFNIUM COMPLEXES. 1992, 64(12), 1897
  151779. 910 PURE AND APPLIED CHEM. A REVIEW
  151780. GABRIEL WEATHERHEAD
  151781. 7174N
  151782. 2/28/96V
  151783. NARASAKA, KOICHI. CHIRAL REAGENTS FOR ASYMMETRIC CONSTRUCTION OF CARBON FRAMEWORKS. 1992, 64(12),1889
  151784. 96 PURE AND APPLIED CHEM. A REVIEWa
  151785. GABRIEL WEATHERHEAD
  151786. 7175N
  151787. 2/28/96V
  151788. COSSY, JANINE. REGIO
  151789.  AND STEREOSELECTIVE CYCLIZATIONS. APPLICATION TO NATURAL PRODUCTS SYNTHESIS. 1992, 64(12),1883
  151790. 8 PURE AND APPLIED CHEM. A REVIEWa
  151791. GABRIEL WEATHERHEAD
  151792. 7176N
  151793. 2/28/96VzLAUTENS, MARK. NEW METHODS FOR THE CONTROL OF MULTIPLE STEREOCENTERS. 1992, 64(12),1873
  151794. 82 PURE AND APPLIED CHEM. A REVIEWa
  151795. GABRIEL WEATHERHEAD
  151796. 7177N
  151797. 2/28/96
  151798. FERINGA, BEN L.; DE LANGE, BEN; JANSEN, JOHAN F. G. A.; DE JONG, JOHANNES C.; LUBBEN, MARCEL; FABER, WIJNAND; SCHUDDE, EBE P. NEW APPROACHES IN ASYMMETRIC SYNTHESIS USING 
  151799. ALKOXYBUTENOLIDES. 1992, 64(12),1865
  151800. 71 PURE AND APPLIED CHEM. A REVIEWa
  151801. GABRIEL WEATHERHEAD
  151802. 7178N
  151803. 2/28/96V
  151804. NORMANT, JEAN F.; MAREK, ILANE; LEFRANCOIS, JEAN MICHEL. ORGANOBIS METALLIC ZINC REAGENTS: THEIR PREPARATION AND USE IN DIASTEREO SELECTIVE REACTIONS. 1992, 64(12), 1857
  151805. 64 PURE AND APPLIED CHEM. A REVIEWa
  151806. GABRIEL WEATHERHEAD
  151807. 7179N
  151808. 2/28/96V
  151809. GHOSEZ, LEON; GENICOT, CHRISTOPHE; GOUVERNEUR, VERONIQUE. CHIRAL AMIDES IN ASYMMETRIC SYNTHESIS. 1992, 64(12),1849
  151810. 56 PURE AND APPLIED CHEM. A REVIEWa
  151811. GABRIEL WEATHERHEAD
  151812. 7180N
  151813. 2/28/96V
  151814. PATERSON, IAN. NEW METHODS AND STRATEGIES FOR THE STEREOCONTROLLED SYNTHESIS OF POLYPROPIONATE
  151815. DERIVED NATURAL PRODUCTS. 1992, 64(12),1821
  151816. 30 PURE AND APPLIED CHEM. A REVIEWa
  151817. GABRIEL WEATHERHEAD
  151818. 7181N
  151819. 2/28/96V
  151820. OVERMAN, LARRY E.; ABELMAN, MATTHEW M.; KUCERA, DAVID J.; TRAN, VINH D.; RICCA, DANIEL J. PALLADIUM
  151821. CATALYZED POLYENE CYCLIZATIONS. 1992, 64(12),1813
  151822. 19 PURE AND APPLIED CHEM. A REVIEWa
  151823. GABRIEL WEATHERHEAD
  151824. 7182N
  151825. 2/28/96V
  151826. STORK, GILBERT; HUTCHINSON, D.; OKABE, M.; PARKER, D.; RA, CHOON SUP; RIBEREAU, F.; SUZUKI, T.; ZEBOVITZ, T. A TOTAL SYNTHESIS OF CALCITRIOL. 1992, 64(12),1809
  151827. 12 PURE AND APPLIED CHEM. A REVIEWa
  151828. GABRIEL WEATHERHEAD
  151829. 7183N
  151830. 2/28/96V
  151831. ENGBERTS, JAN B. F. N. CATALYSIS BY SURFACTANT AGGREGATES IN AQUEOUS SOLUTIONS. 1992, 64(11),1653
  151832. 60 PURE AND APPLIED CHEM. A REVIEWa
  151833. GABRIEL WEATHERHEAD
  151834. 7184N
  151835. 2/28/96V
  151836. SIMANDI, L. I.; BARNA, T.; SZEVERENYI, Z.; NEMETH, S. HOMOGENEOUS CATALYTIC OXIDATION OF O
  151837. SUBSTITUTED ANILINES WITH DIOXYGEN IN THE PRESENCE OF COBALT AND MANGANESE COMPLEXES. 1992, 64(10),1511
  151838. 18 PURE AND APPLIED CHEM. A REVIEWa
  151839. GABRIEL WEATHERHEAD
  151840. 2/28/96V
  151841. LEVASHOV, A. V. MICROHETEROGENEOUS SURFACTANT
  151842. BASED SYSTEMS AS THE MEDIA FOR ENZYMIC REACTIONS. 1992, 64(8),1125
  151843. 8 PURE AND APPLIED CHEM. A REVIEWa
  151844. GABRIEL WEATHERHEAD
  151845. 7186N
  151846. 2/28/96V
  151847. BASAVAIAH, DEEVI; KRISHNA, PEDDINTI RAMA. ENANTIOSELECTIVE SYNTHESIS USING CRUDE ENZYMES. 1992, 64(8), 1067
  151848. 72 PURE AND APPLIED CHEM. A REVIEWa
  151849. GABRIEL WEATHERHEAD
  151850. 7187N
  151851. 2/28/96V
  151852. PETITOU, M.; VAN BOECKEL, C. A. A. CHEMICAL SYNTHESIS OF HEPARIN FRAGMENTS AND ANALOGUES. 1992, 60, 143
  151853. 210 PROGRESS IN THE CHEM. OF ORG. NATURAL PRODUCTS. A REVIEWa
  151854. GABRIEL WEATHERHEAD
  151855. 7188N
  151856. 2/28/96V
  151857. WAHLBERG, I.; EKLUND, A.
  151858. M. CYCLIZED CEMBRANOIDS OF NATURAL OCCURRENCE. 1992, 60,1
  151859. 141 PROGRESS IN THE CHEM. OF ORG. NATURAL PRODUCTS. A REVIEWa
  151860. GABRIEL WEATHERHEAD
  151861. 7189N
  151862. 2/28/96
  151863. WAHLBERG, I.; EKLUND, A.
  151864. M. CEMBRANOIDS, PSEUDOPTERANOIDS, AND CUBITANOIDS OF NATURAL OCCURRENCE. 1992,59,141
  151865. 294 PROGRESS IN THE CHEM. OF ORG. NATURAL PRODUCTS. A REVIEWa
  151866. GABRIEL WEATHERHEAD
  151867. 7190N
  151868. 2/28/96VwHATANAKA, SHIN
  151869. ICHI. AMINO ACIDS FROM MUSHROOMS. 1992,59,1
  151870. 140 PROGRESS IN THE CHEM. OF ORG. NATURAL PRODUCTS. A REVIEWa
  151871. GABRIEL WEATHERHEAD
  151872. 7191N
  151873. 2/28/96
  151874. KAMLET, MORTIMER J. LINEAR SOLVATION ENERGY RELATIONSHIPS: AN IMPROVED EQUATION FOR CORRELATION AND PREDICTION OF AQUEOUS SOLUBILITIES OF AROMATIC SOLUTES INCLUDING POLYCYCLIC AROMATIC HYDROCARBONS AND POLYCHLORINATED BIPHENYLS. 1993,19, 295
  151875. 317 PROGRESS IN PHYS. ORG. CHEM. A REVIEW
  151876. GABRIEL WEATHERHEAD
  151877. 7192N
  151878. 2/28/96V
  151879. EXNER, OTTO; FRIEDL, ZDENEK; TESSEK LABORATORY. TRANSMISSION OF SUBSTITUENT EFFECTS: THE THROUGH
  151880. SPACE AND THROUGH
  151881. BOND MODELS AND THEIR EXPERIMENTAL VERIFICATION. 1993,19, 259
  151882. 94 PROGRESS IN PHYS. ORG. CHEM. A REVIEW
  151883. GABRIEL WEATHERHEAD
  151884. 7193N
  151885. 2/28/96V
  151886. EDLUND, ULF; BUNCEL, ERWIN. ELECTRONIC CONFIGURATION, STRUCTURE, AND SOLVATION OF PHENYL
  151887. SUBSTITUTED GROUP IVA ANIONS. 1993,19, 225
  151888. 58 PROGRESS IN PHYS. ORG. CHEM. A REVIEWa
  151889. GABRIEL WEATHERHEAD
  151890. 7194N
  151891. 2/28/96V
  151892. BOWDEN, KENNETH; GRUBBS, EDWARD J. ANGULAR DEPENDENCE OF DIPOLAR SUBSTITUENT EFFECTS. 1993,19,183
  151893. 224 PROGRESS IN PHYS. ORG. CHEM. A REVIEWa
  151894. GABRIEL WEATHERHEAD
  151895. 7195N
  151896. 2/28/96V
  151897. ABBOUD, JOSE
  151898. LUIS M.; NOTARIO, RAFAEL; BERTRAN, JUAN; SOLA, MIQUEL. ONE CENTURY OF PHYSICAL ORGANIC CHEMISTRY: THE MENSHUTKIN REACTION. 1993,19,1
  151899. 182 PROGRESS IN PHYS. ORG. CHEM. A REVIEWa
  151900. GABRIEL WEATHERHEAD
  151901. 7196N
  151902. 2/28/96VtKROW, GRANT R. THE BAYER
  151903. VILLIGER OXIDATION OF KETONES AND ALDEHYDES. 1993, 43, 251
  151904. 798 ORGANIC. REACTIONS. A REVIEWa
  151905. GABRIEL WEATHERHEAD
  151906. 7197N
  151907. 2/28/96
  151908. VkWILSON, STEPHEN R. ANION
  151909. ASSISTED SIGMATROPIC REARRANGEMENTS. 1993, 43, 93
  151910. 250 ORGANIC. REACTIONS. A REVIEWa
  151911. GABRIEL WEATHERHEAD
  151912. 7198N
  151913. 2/28/96V
  151914. PINE, STANLEY H. CARBONYL METHYLENATION AND ALKYLIDENATION USING TITANIUM
  151915. BASED REAGENTS. 1993, 43, 1
  151916. 92 ORGANIC. REACTIONS. A REVIEWa
  151917. GABRIEL WEATHERHEAD
  151918. 7199N
  151919. 2/28/96VVHUGHES, DAVID L. THE MITSUNOBU REACTION. 1992, 42,335
  151920. 656 ORGANIC. REACTIONS. A REVIEWa
  151921. GABRIEL WEATHERHEAD
  151922. 7200N
  151923. 2/28/96V~RABIDEAU, PETER W.; MARCINOW, ZBIGNIEW. THE BIRCH REDUCTION OF AROMATIC COMPOUNDS. 1992, 42,1
  151924. 334 ORGANIC. REACTIONS. A REVIEWa
  151925. GABRIEL WEATHERHEAD
  151926. 7201N
  151927. 2/28/96V
  151928. MARCACCINI, S.; TORROBA, T. THE USE OF ISOCYANIDES IN HETEROCYCLIC SYNTHESIS. 1993, 25(2),141
  151929. 208 ORG. PREP. AND PROC. INT. A REVIEWa
  151930. GABRIEL WEATHERHEAD
  151931. 7202N
  151932. 2/28/96
  151933. CRIMMINS, M. T.; NANTERMET, P. G. HOMOENOLATES AND OTHER FUNCTIONALIZED ORGANOMETALLICS. 1993, 25(1), 41
  151934. 81 ORG. PREP. AND PROC. INT. A REVIEWa
  151935. GABRIEL WEATHERHEAD
  151936. 7203N
  151937. 2/28/96V
  151938. SIBI, M. P. CHEMISTRY OF N
  151939. METHOXY
  151940. METHYLAMIDES. APPLICATIONS IN SYNTHESIS. 1993, 25(1),15
  151941. 40 ORG. PREP. AND PROC. INT. A REVIEWa
  151942. GABRIEL WEATHERHEAD
  151943. 7204N
  151944. 2/28/96V
  151945. POLLARD, RENEE; WAN, PETER. SYNTHETIC APPLICATIONS OF DIARYL ETHER PHOTOCHEMISTRY. 1993, 25(1),1
  151946. 14 ORG. PREP. AND PROC. INT. A REVIEWa
  151947. GABRIEL WEATHERHEAD
  151948. 7205N
  151949. 2/28/96VmHANSON, J. R. STEROIDS: REACTIONS AND PARTIAL SYNTHESES. 1992, 9(6), 581
  151950. 95 NATURAL PRODUCT REPORTS. A REVIEWa
  151951. GABRIEL WEATHERHEAD
  151952. 7206N
  151953. 2/28/96VZFRAGA, B. M. NATURAL SESQUITERPENOIDS. 1992,9(6), 557
  151954. 80 NATURAL PRODUCT REPORTS. A REVIEWa
  151955. GABRIEL WEATHERHEAD
  151956. 7207N
  151957. 2/28/96
  151958. VSGRAYSON, D. H. MONOTERPENOIDS. 1992, 9(6), 531
  151959. 56 NATURAL PRODUCT REPORTS. A REVIEWa
  151960. GABRIEL WEATHERHEAD
  151961. 7208N
  151962. 2/28/96V
  151963. HERBERT, R. B. THE BIOSYNTHESIS OF PLANT ALKALOIDS AND NITROGENOUS MICROBIAL METABOLITES. 1992, 9(6), 507
  151964. 29 NATURAL PRODUCT REPORTS. A REVIEWa
  151965. GABRIEL WEATHERHEAD
  151966. 7209N
  151967. 2/28/96V
  151968. PINDER, A. R. AZETIDINE, PYRROLE, PYRROLIDINE, PIPERIDINE, AND PYRIDINE ALKALOIDS. 1992, 9(5), 491
  151969. 504 NATURAL PRODUCT REPORTS. A REVIEWa
  151970. GABRIEL WEATHERHEAD
  151971. 7210N
  151972. 2/28/96VlO'HAGAN, DAVID. BIOSYNTHESIS OF POLYKETIDE METABOLITES. 1992, 9(5), 447
  151973. 79 NATURAL PRODUCT REPORTS. A REVIEWa
  151974. GABRIEL WEATHERHEAD
  151975. 7211N
  151976. 2/28/96V
  151977. SAXTON, J. E. RECENT PROGRESS IN THE CHEMISTRY OF INDOLE ALKALOIDS AND MOLD METABOLITES. 1992, 9(5), 393
  151978. 446 NATURAL PRODUCT REPORTS. A REVIEWa
  151979. GABRIEL WEATHERHEAD
  151980. 7212N
  151981. 2/28/96
  151982. VmALVAREZ, MERCEDES; JOULE, JOHN A. SYNTHESIS OF PYRIDOACRIDINES. 1992, 34(12), 2385
  151983. 405 HETEROCYCLES. A REVIEWa
  151984. GABRIEL WEATHERHEAD
  151985. 7213N
  151986. 2/28/96V
  151987. KATRITZKY, ALAN R.; FAN, WEI QIANG. MECHANISMS AND RATES OF ELECTRO PHILIC SUBSTITUTION REACTIONS OF HETEROCYCLES. 1992, 34(11), 2179
  151988. 229 HETEROCYCLES. A REVIEWa
  151989. GABRIEL WEATHERHEAD
  151990. 7214N
  151991. 2/28/96V
  151992. RADL, STANISLAV; BOUZARD, DANIEL. RECENT ADVANCES IN THE SYNTHESIS OF ANTIBACTERIAL QUINOLINES. 1992, 34(11), 2143
  151993. 77 HETEROCYCLES. A REVIEWa
  151994. GABRIEL WEATHERHEAD
  151995. 7215N
  151996. 2/28/96V
  151997. BOX, VERNON G. S. THE SIGNIFICANCE OF THE BOND LENGTHS AND BOND ORDERS OF CONJUGATED UNSATURATED ORGANIC MOLECULES. THE ROLE OF HETERO
  151998. AROMATICITY IN THE TERTIARY STRUCTURES OF DNA. 1992, 34(8),1631
  151999. 59 HETEROCYCLES. A REVIEWa
  152000. GABRIEL WEATHERHEAD
  152001. 7216N
  152002. 2/28/96VkSILVESTER, MICHAEL J. LANDMARKS IN ORGANOFLUORINE CHEMISTRY. 1993, 29(3), 215
  152003. 18 CHEM. IN BRITAIN. A REVIEW
  152004. GABRIEL WEATHERHEAD
  152005. 7217N
  152006. 2/28/96V`HARRIS, KENNETH D. M. MOLECULAR CONFINEMENT. 1993, 29(2), 132
  152007. 36, 138 CHEM. IN BRITAIN. A REVIEWa
  152008. GABRIEL WEATHERHEAD
  152009. 7218N
  152010. 2/28/96VkNOE, CHRISTIAN; BADER, ALFRED. FACTS ARE BETTER THAN DREAMS. 1993, 29(2), 126
  152011. 36 CHEM. IN BRITAIN. A REVIEWa
  152012. GABRIEL WEATHERHEAD
  152013. 7219N
  152014. 2/28/96VYENGEL, MICHAEL. A PROJECTION ON FISCHER. 1992, 28(12), 1106
  152015. 09 CHEM. IN BRITAIN. A REVIEWa
  152016. GABRIEL WEATHERHEAD
  152017. 7220N
  152018. 2/28/96VhHUTCHINGS, GRAHAM. CATALYSIS IN INTRACRYSTALLINE SPACE. 1992, 28(11), 1006
  152019. 09 CHEM. IN BRITAIN. A REVIEWa
  152020. GABRIEL WEATHERHEAD
  152021. 7221N
  152022. 2/28/96V{WEBB, GEOFFREY; WINFIELD, JOHN. NEW ROUTES TO ALTERNATIVE HALOCARBONS. 1992, 28(11), 996
  152023. 97,1002 CHEM. IN BRITAIN. A REVIEWa
  152024. GABRIEL WEATHERHEAD
  152025. 7222N
  152026. 2/28/96
  152027. VpMEYER, MARION; O'HAGAN, DAVID, RARE FLUORINATED NATURAL PRODUCTS. 1992, 28(9), 785
  152028. 88 CHEM. IN BRITAIN. A REVIEWa
  152029. GABRIEL WEATHERHEAD
  152030. 7223N
  152031. 2/28/96VvMCKERVEY, ANTHONY; BOHMER, VOLKER. CALIXARENES
  152032. SUPRAMOLECULAR PURSUITS. 1992, 28(8), 724
  152033. 27 CHEM. IN BRITAIN. A REVIEWa
  152034. GABRIEL WEATHERHEAD
  152035. 7224N
  152036. 2/28/96V
  152037. JEFFORD, CHARLES W. THE PHOTO
  152038. OXYGENATION OF OLEFINS AND THE ROLE OF ZWITTERIONIC PEROXIDES. 1993, 22(1), 59
  152039. 66 CHEM. SOC. REV. A REVIEWa
  152040. GABRIEL WEATHERHEAD
  152041. 7225N
  152042. 2/28/96VyBROWN, JOHN M. SELECTIVITY AND MECHANISM IN CATALYTICAL ASYMMETRIC SYNTHESIS. 1993, 22(1), 25
  152043. 41 CHEM. SOC. REV. A REVIEWa
  152044. GABRIEL WEATHERHEAD
  152045. 7226N
  152046. 2/28/96V
  152047. ARNETT, EDWARD M.; FLOWERS, ROBERT A., II. BOND CLEAVAGE ENERGIES OF MOLECULES AND THEIR ASSOCIATED RADICAL IONS. 1993, 22(1), 9
  152048. 15 CHEM. SOC. REV. A REVIEWa
  152049. GABRIEL WEATHERHEAD
  152050. 7227N
  152051. 2/28/96
  152052. LICKISS, PAUL D. TRANSITION METAL COMPLEXES OF SILYLENES, SILENES, DISILENES, AND RELATED SPECIES. 1992,21(4), 271
  152053. 9 CHEM. SOC. REV. A REVIEWa
  152054. GABRIEL WEATHERHEAD
  152055. 7228N
  152056. 2/28/96VoDELOUX, LAURENT; SREBNIK, MORRIS. ASYMMETRIC BORON
  152057. CATALYZED REACTIONS. 1993, 93(2), 763
  152058. 84 CHEM. REV. A REVIEWa
  152059. GABRIEL WEATHERHEAD
  152060. 7229N
  152061. 2/28/96V
  152062. PINDUR, ULF; LUTZ, GUNDULA; OTTO, CHRISTIAN. ACCELERATION AND SELECTIVITY ENHANCEMENT OF DIELS
  152063. ALDER REACTIONS BY SPECIAL AND CATALYTIC METHODS. 1993, 93(2), 741
  152064. 61 CHEM. REV. A REVIEWa
  152065. GABRIEL WEATHERHEAD
  152066. 7230N
  152067. 2/28/96V
  152068. RUDCHENKO, VLADIMIR F. SYNTHESIS, REACTIONS AND PROPERTIES OF OXYGEN
  152069. NITROGEN
  152070. OXYGEN SYSTEMS. 1993, 93(2), 725
  152071. 39 CHEM. REV. A REVIEWa
  152072. GABRIEL WEATHERHEAD
  152073. 7231N
  152074. 2/28/96VjCORNELISSE, JAN. THE META PHOTOCYCLOADDITION OF ARENES TO ALKENES. 1993, 93(2), 615
  152075. 69 CHEM. REV. A REVIEWa
  152076. GABRIEL WEATHERHEAD
  152077. 7232N
  152078. 2/28/96
  152079. WAN, PETER; SHUKLA, DEEPAK. UTILITY OF ACID
  152080. BASE BEHAVIOR OF EXCITED STATES OF ORGANIC MOLECULES. 1993, 93(1), 571
  152081. 84 CHEM. REV. A REVIEWa
  152082. GABRIEL WEATHERHEAD
  152083. 7233N
  152084. 2/28/96V
  152085. BHATTACHARYYA, KANKAN; CHOWDHURY, MIHIR. ENVIRONMENTAL AND MAGNETIC FIELD EFFECTS ON EXCIPLEX AND TWISTED CHARGE TRANSFER EMISSION. 1993, 93(1), 507
  152086. 35 CHEM. REV. A REVIEWa
  152087. GABRIEL WEATHERHEAD
  152088. 7234N
  152089. 2/28/96V
  152090. LEIGH, WILLIAM J. TECHNIQUES AND APPLICATIONS OF FAR
  152091. UV PHOTOCHEMISTRY IN SOLUTION. THE PHOTOCHEMISTRY OF THE C3H4 AND C4H6 HYDROCARBONS. 1993, 93(1), 487
  152092. 505 CHEM. REV. A REVIEWa
  152093. GABRIEL WEATHERHEAD
  152094. 7235N
  152095. 2/28/96V
  152096. DUXBURY, DEBRA FAYE. THE PHOTOCHEMISTRY AND PHOTOPHYSICS OF TRIPHENYLMETHANE DYES IN SOLID AND LIQUID MEDIA. 1993, 93(1), 381
  152097. 433 CHEM. REV. A REVIEWa
  152098. GABRIEL WEATHERHEAD
  152099. 7236N
  152100. 2/28/96
  152101. DE KEUKELEIRE, DENIS; HE, SHU LIN. PHOTOCHEMICAL STRATEGIES FOR THE CONSTRUCTION OF POLYCYCLIC MOLECULES. 1993, 93(1), 359
  152102. 80 CHEM. REV. A REVIEWa
  152103. GABRIEL WEATHERHEAD
  152104. 7237N
  152105. 2/28/96VbJOHNSTON, L. J. PHOTOCHEMISTRY OF RADICALS AND BIRADICALS. 1993, 93(1), 251
  152106. 66 CHEM. REV. A REVIEWa
  152107. GABRIEL WEATHERHEAD
  152108. 7238N
  152109. 2/28/96V
  152110. WILSON, R. MARSHALL; SCHNAPP, KARLYN A. HIGH INTENSITY LASER PHOTOCHEMISTRY OF ORGANIC MOLECULES IN SOLUTION. 1993, 93(1), 223
  152111. 49 CHEM. REV. A REVIEWa
  152112. GABRIEL WEATHERHEAD
  152113. 7239N
  152114. 2/28/96V
  152115. GEHLEN, MARCELO H.; DE SCHRYVER, FRANS C. TIME
  152116. RESOLVED FLUORESCENCE QUENCHING IN MICELLAR ASSEMBLIES. 1993, 93(1), 199
  152117. 221 CHEM. REV. A REVIEWa
  152118. GABRIEL WEATHERHEAD
  152119. 7240N
  152120. 2/28/96VgBECKER, HANS DIETER. UNIMOLECULAR PHOTOCHEMISTRY OF ANTHRACENES. 1993, 93(1),145
  152121. 72 CHEM. REV. A REVIEWa
  152122. GABRIEL WEATHERHEAD
  152123. 7241N
  152124. 2/28/96
  152125. MUELLER, FELIX; MATTAY, JOCHEN. PHOTOCYCLOADDITIONS: CONTROL BY ENERGY AND ELECTRON TRANSFER. 1993, 93(1), 99
  152126. 117 CHEM. REV. A REVIEWa
  152127. GABRIEL WEATHERHEAD
  152128. 7242N
  152129. 2/28/96V
  152130. MACIEJEWSKI, ANDRZEJ; STEER, RONALD P. THE PHOTOPHYSICS, PHYSICAL PHOTOCHEMISTRY, AND RELATED SPECTROSCOPY OF THIOCARBONYLS. 1993, 93(1), 67
  152131. 98 CHEM. REV. A REVIEWa
  152132. GABRIEL WEATHERHEAD
  152133. 7243N
  152134. 2/28/96VwGIVENS, RICHARD S.; KUEPER, L. WILLIAM, III. PHOTOCHEMISTRY OF PHOSPHATE ESTERS. 1993, 93(1), 55
  152135. 66 CHEM. REV. A REVIEWa
  152136. GABRIEL WEATHERHEAD
  152137. 7244N
  152138. 2/28/96VXKOHLER, BRYAN E. OCTATETRAENE PHOTOISOMERIZATION. 1993, 93(1), 41
  152139. 54 CHEM. REV. A REVIEWa
  152140. GABRIEL WEATHERHEAD
  152141. 7245N
  152142. 2/28/96V
  152143. ARAI, TATSUO; TOKUMARU, KATSUMI. PHOTOCHEMICAL ONE
  152144. WAY ADIABATIC ISOMERIZATION OF AROMATIC OLEFINS. 1993, 93(1), 23
  152145. 39 CHEM. REV. A REVIEWa
  152146. GABRIEL WEATHERHEAD
  152147. 7246N
  152148. 2/28/96
  152149. SCHUSTER, DAVID I.; LEM, GEORGE; KAPRINIDIS, NIKOLAS A. NEW INSIGHTS INTO AN OLD MECHANISM: [2 + 2] PHOTOCYCLOADDITION OF ENONES TO ALKENES. 1993, 93(1), 3
  152150. 22 CHEM. REV. A REVIEWa
  152151. GABRIEL WEATHERHEAD
  152152. 7247N
  152153. 2/28/96V
  152154. BOLM, CARSTEN. ENANTIOSELECTIVE TRANSITION METAL
  152155. CATALYZED HYDROGENATION FOR THE ASYMMETRIC SYNTHESIS OF AMINES. 1993, 32(2), 232
  152156. 3 ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152157. GABRIEL WEATHERHEAD
  152158. 7248N
  152159. 2/28/96
  152160. 7UGI, IVAR; BAUER, JOHANNES; BLEY, KLEMENS; DENGLER, ALF; DIETZ, ANDREAS; FONTAIN, ERIC; GRUBER, BERNHARD, ET AL. COMPUTER
  152161. ASSISTED SOLUTION OF CHEMICAL PROBLEMS. THE HISTORICAL DEVELOPMENT AND THE PRESENT STATE OF THE ART OF A NEW DISCIPLINE OF CHEMISTRY. 1993, 32(2), 201
  152162. 27 ANGE CHEM., INT. ED. ENGL. A REVIEW
  152163. GABRIEL WEATHERHEAD
  152164. 7249N
  152165. 2/28/96VuFURSTNER, ALOIS. CHEMISTRY OF AND WITH HIGHLY REACTIVE METALS. 1993, 32(2),164
  152166. 89 ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152167. GABRIEL WEATHERHEAD
  152168. 7250N
  152169. 2/28/96V
  152170. TIETZE, LUTZ F.; BEIFUSS, UWE. SEQUENTIAL TRANSFORMATIONS IN ORGANIC CHEMISTRY: A SYNTHETIC STRATEGY WITH A FUTURE. 1993, 32(2),131
  152171. 63 ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152172. GABRIEL WEATHERHEAD
  152173. 7251N
  152174. 2/28/96V
  152175. MICHAEL, JOSEPH P.; PATTENDEN, GERALD. MARINE METABOLITES AND METAL ION CHELATION: THE FACTS AND THE FANTASIES. 1993, 32(1), 1
  152176. 23 ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152177. GABRIEL WEATHERHEAD
  152178. 7252N
  152179. 2/28/96V
  152180. MEKELBURGER, HANS BERNHARD; JAWOREK, WILFRIED; VOGTLE, FRITZ. DENDRIMERS, ARBOROLS AND CASCADE MOLECULES: BREAKTHROUGH INTO GENERATIONS OF NEW MATERIALS. 1992, 31(12), 1571
  152181. 6.  ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152182. GABRIEL WEATHERHEAD
  152183. 7253N
  152184. 2/28/96V
  152185. LICHTENTHALER, FRIEDER W. EMIL FISCHER'S PROOF OF THE CONFIGURATION OF SUGARS. A CENTENNIAL TRIBUTE. 1992, 31(12), 1541
  152186. 56 ANGE CHEM., INT. ED. ENGL. A REVIEWa
  152187. GABRIEL WEATHERHEAD
  152188. 7254N
  152189. 2/28/96
  152190. VtPEREIRA, SCHUBERT; SREBNIK, MORRIS. THE IRELAND
  152191. CLAISEN REARRANGEMENT. 1993, 26(1),17
  152192. 29 ALDRICHIMICA ACTA. A REVIEWa
  152193. GABRIEL WEATHERHEAD
  152194. 7255N
  152195. 2/28/96VcFRY, ALBERT J. ELECTROCHEMISTRY IN ORGANIC SYNTHESIS. 1993, 26(1), 3
  152196. 11 ALDRICHIMICA ACTA. A REVIEWa
  152197. GABRIEL WEATHERHEAD
  152198. 7256N
  152199. 2/28/96V}MOTHERWELL, WILLIAM B. A CURIOSITY DRIVEN RESEARCH FOR NEW CHEMICAL REACTIONS. 1992, 25(3), 71
  152200. 80 ALDRICHIMICA ACTA. A REVIEWa
  152201. GABRIEL WEATHERHEAD
  152202. 7257N
  152203. 2/28/96VgSEEBACH, DIETER. HOW WE STUMBLED INTO PEPTIDE CHEMISTRY. 1992, 25(3), 59
  152204. 66 ALDRICHIMICA ACTA. A REVIEWa
  152205. GABRIEL WEATHERHEAD
  152206. 7258N
  152207. 2/28/96V
  152208. SIMKIN, B. YA.; MINKIN, V. I.; GLUKHOVTSEV, M. N. THE CONCEPT OF AROMATICITY IN HETEROCYCLIC CHEMISTRY. 1993, 56, 304 ADVANCES IN HETEROCYCLIC CHEMISTRY. A REVIEWa
  152209. GABRIEL WEATHERHEAD
  152210. 7259N
  152211. 2/28/96
  152212. REWCATLE, GORDON W.; KATRITZKY, ALAN R. GENERATION AND REACTIONS OF SP2
  152213. CARBANIONIC CENTERS IN THE VICINITY OF HETEROCYCLIC NITROGEN ATOMS. 1993, 56,157 ADVANCES IN HETEROCYCLIC CHEMISTRY. A REVIEWa
  152214. GABRIEL WEATHERHEAD
  152215. 7260N
  152216. 2/28/96V
  152217. VIVONA, NICOLO; BUSCEMI, SILVESTRE; FRENNA, VINCENZO; CUSMANO, GIUSEPPE. RING TRANSFORMATIONS OF FIVE
  152218. MEMBERED HETEROCYCLES. 1993, 56, 50 ADVANCES IN HETEROCYCLIC CHEMISTRY. A REVIEWa
  152219. GABRIEL WEATHERHEAD
  152220. 7261N
  152221. 2/28/96V
  152222. LLOYD, DOUGLAS; MCNAB, HAMISH. 2,3
  152223. DIHYDRO
  152224. DIAZEPINES AND 2,3
  152225. DIHYDRO
  152226. DIAZEPINIUM SALTS. 1993, 56, 1 ADVANCES IN HETERO CYCLIC CHEMISTRY. A REVIEWa
  152227. GABRIEL WEATHERHEAD
  152228. 7262N
  152229. 2/28/96VxFLOSS, HEINZ, G.; LEE, SUNGSOOK. CHIRAL METHYL GROUPS: SMALL IS BEAUTIFUL. 1993, 26 (3),116
  152230. 22 ACC. CHEM. RES.  A REVIEWa
  152231. GABRIEL WEATHERHEAD
  152232. 7263N
  152233. 2/28/96
  152234. VpDAVIS, MARK E. NEW VISTAS IN ZEOLITE AND MOLECULAR SIEVE CATALYSIS. 1993, 26 (3) 111
  152235. 15 ACC. CHEM. RES. A REVIEWa
  152236. GABRIEL WEATHERHEAD
  152237. 7264N
  152238. 2/28/96V
  152239. CARNAHAN, EDMUND M.; PROTASIEWICZ, JOHN D.; LIPPARD, STEPHEN J. 15 YEARS OF REDUCTIVE COUPLING: WHAT HAVE WE LEARNED? 1993, 26(3), 90
  152240. 7 ACC. CHEM. RES. A REVIEWa
  152241. GABRIEL WEATHERHEAD
  152242. 7265N
  152243. 2/28/96V
  152244. NICKON, ALEX. NEW PERSPECTIVES ON CARBENE REARRANGEMENTS: MIGRATORY APTITUDES, BYSTANDER ASSISTANCE, AND GEMINAL EFFICIENCY. 1993, 26(3), 84
  152245. 9 ACC. CHEM. RES. A REVIEWa
  152246. GABRIEL WEATHERHEAD
  152247. 7266N
  152248. 2/28/96V
  152249. HOZ, SHMARYAHU. IS THE TRANSITION STATE INDEED INTERMEDIATE BETWEEN REACTANTS AND PRODUCTS? THE MICHAEL ADDITION REACTION AS A CASE STUDY. 1993, 26(2), 69
  152250. 74 ACC. CHEM. RES. A REVIEWa
  152251. GABRIEL WEATHERHEAD
  152252. 7267N
  152253. 2/28/96V{PAQUETTE, LEO A. THE CURRENT VIEW OF DYNAMIC CHANGE WITHIN CYCLOOCTATETRAENES.  1993, 26(2), 57
  152254. 62 ACC. CHEM. RES. A REVIEW
  152255. GABRIEL WEATHERHEAD
  152256. 7268N
  152257. 2/28/96V
  152258. LEGZDINS, PETER; VELTHEER, JOHN E. CP'M(NO)R2: 16
  152259. ELECTRON PIANO
  152260. STOOL MOLECULES OF MOLYBDENUM AND TUNGSTEN. 1993, 26(2), 41
  152261. 8 ACC. CHEM. RES. A REVIEWa
  152262. GABRIEL WEATHERHEAD
  152263. ORG PREP PROCEDURE INTC
  152264. MARCACCINI SM
  152265. 7269N
  152266. 2/28/96V;THE USE OF ISOCYANIDES IN HETEROCYCLIC SYNTHESIS 
  152267.  A REVIEWW
  152268. 1993 APRX
  152269. 25(2)a
  152270. GABRIEL WEATHERHEAD
  152271. J ORGANOMETAL CHEMC
  152272. SCHMAUCKS GM
  152273. 7270N
  152274. 2/28/96V8ORGANOSILOXANES WITH FUNCTIONAL GROUPS 
  152275.  A SHORT REVIEW.W
  152276. 1993 MAR 9X
  152277. 446(1
  152278. GABRIEL WEATHERHEAD
  152279. J ORG CHEMCsDITTMER CHIRAL ASYMMETRIC EPOXIDATION TELLURIUM SHARPLESS
  152280. KATSUKI REVIEW KINETIC RESOLUTION ALLYLIC EPOXIDE ALCOHOLM
  152281. 7271N
  152282. 2/28/96V
  152283. A TELLURIUM TRANSPOSITION ROUTE TO ALLYLIC ALCOHOLS.  OVERCOMING SOME LIMITATIONS OF THE SHARPLESS
  152284. KATSUKI ASYMMETRIC EPOXIDATIONW
  152285. VOL 58 1993 P 718a
  152286. GABRIEL WEATHERHEAD
  152287. CYYAN ALDOL ASYMMETRIC REVIEW CHIRAL METAL CHELATION EVANS DIASTEREOSELECTIVITY OXAZOLIDONEM
  152288. 7272N
  152289. 2/28/96VwASYMMETRIC ALDOL REACTIONS.  A NOVEL MODEL FOR SWITCHING BETWEEN CHELATION AND NON CHELATION CONTROLLED ALDOL REACTIONSW
  152290. VOL 115 1993 P 2613a
  152291. GABRIEL WEATHERHEAD
  152292. ACC CHEM RESC_PAQUETTE CYCLOOCTATETRAENE RING INVERSION REVIEW RACEMIZATION SUBSTITUTION ANNULATED BOND SHIFTM
  152293. 7273N
  152294. 2/28/96V<THE CURRENT VIEW OF DYNAMIC CHANGE WITHIN CYCLOOCTATETRAENESW
  152295. VOL 26 1993 P 57a
  152296. GABRIEL WEATHERHEAD
  152297. SYNLETTC:BROWN REVIEW CARBENE FLASH REARRANGEMENT KETENES EXTRUSIONM
  152298. 7274N
  152299. 2/28/96VYGAS PHASE CHEMISTRY OF KETENES, CARBENES, ACETYLENES AND ARYNES.  FLASH VACUUM PYROLYSIS.W
  152300. 1993 P 9a
  152301. GABRIEL WEATHERHEAD
  152302. J ORG CHEMCgCRIMMINS CONJUGATE ADDITION 3+2 ENOLATE ZINC ALKYNE ESTER ACETYLENE CYCLOPENTENONE REVIEW CYCLOHEXENONEM
  152303. 7275N
  152304. 2/28/96VZADDITION OF ZINC HOMOENOLATES TO ACETYLENIC ESTERS AND AMIDES.  A FORMAL 3+2 CYCLOADDITION
  152305. VOL 58 1993 P 1038a
  152306. GABRIEL WEATHERHEAD
  152307. ORG PREP PROCEDURE INTC
  152308. DOUBLE
  152309. HYDROXYLATION REACTION COPPER REAGENTS RCU(CN)ZNI ALPHA
  152310. METHYLENE KETONES TIN
  152311. LITHIUM EXCHANGE ZINC HOMOENOLATE REFORMATSKY REACTION BETA
  152312. ZINC 3
  152313. CARBOETHOXY PROPYLZINC IODIDE 1,4
  152314. DICARBONYL COMPOUNDS PROPIONATE HOMOENOLATE CRIMMINS MTM
  152315. 7276N
  152316. 2/28/96VAHOMOENOLATES AND OTHER FUNCTIONALIZED ORGANOMETALLICS 
  152317.  A REVIEW.W
  152318. 1993 FEBX
  152319. 25(1)a
  152320. GABRIEL WEATHERHEAD
  152321. ORG PREP PROCEDURE INTC
  152322. ALPHA
  152323. AMINO
  152324. ACIDS ORGANOMETALLIC ADDITION
  152325. REACTIONS PROGENITOR PAR EXCELLENCE KETO ESTER DERIVATIVES METAL
  152326. HALOGEN EXCHANGE 3
  152327. SUBSTITUTED PYRROLES EFFICIENT SYNTHESIS IMMUNOSUPPRESSANT (
  152328. 506 PYRANOSIDIC HOMOLOGATION BIS
  152329. HETEROANNULATION SIBI MPM
  152330. 7277N
  152331. 2/28/96VMCHEMISTRY OF N
  152332. METHOXY
  152333. METHYLAMIDES 
  152334.  APPLICATIONS IN SYNTHESIS 
  152335.  A REVIEW.W
  152336. 1993 FEBX
  152337. 25(1)a
  152338. GABRIEL WEATHERHEAD
  152339. ORG PREP PROCEDURE INT
  152340. CbARYL VINYL ETHERS AQUEOUS
  152341. SOLUTION P
  152342. DIOXINS PHOTOCYCLIZATION PHOTOCONVERSION PHOTOLYSIS POLLARD RM
  152343. 7278N
  152344. 2/28/96VASYNTHETIC APPLICATIONS OF DIARYL ETHER PHOTOCHEMISTRY 
  152345.  A REVIEW.W
  152346. 1993 FEBX
  152347. 25(1)a
  152348. GABRIEL WEATHERHEAD
  152349. ORG. REACT.CYLIPSHUTZ; ORGANOCOPPER, SUBSTITUTION, COPPER, CONJUGATE ADDITION, CARBOMETALATION, REVIEWM
  152350. 7279N
  152351. 2/28/96VnORGANOCOPPER REAGENTS: SUBSTITUTION, CONJUGATE ADDITION, CARBOCUPRATION, METALOCUPRATION, AND OTHER REACTIONS.W
  152352. 1992   41   135
  152353. GABRIEL WEATHERHEAD
  152354. NATURAL PRODUCTS REPORTSC8LEWIS, J.R.; ALKALOID, AMARYLLIDACEAE, SCELETIUM, REVIEWM
  152355. 7280N
  152356. 2/28/96V&AMARYLLIDACEAE AND SCELETIUM ALKALOIDSW
  152357. 1992   9   183
  152358. GABRIEL WEATHERHEAD
  152359. TETRAHEDRONCKPOSTEMA; CARBOHYDRATE, REVIEW, CARBON GLYCOSIDE, WITTIG, PALLADIUM, RADICALM
  152360. 7281N
  152361. 2/28/96V4RECENT DEVELOPMENTS IN THE SYNTHESIS OF C
  152362. GLYCOSIDESW
  152363. 1992   48   8545
  152364. 8599a
  152365. GABRIEL WEATHERHEAD
  152366. ClGIULIANO; FRANCK; LOPEZ; HORTON; LEBLANC; DESHONG; KUNZ; LUBINEAU; CARBOHYDRATE, CYCLOADDITION, REVIEW DIENEM
  152367. 7282N
  152368. 2/28/96V1CYCLOADDITION REACTIONS IN CARBOHYDRATE CHEMISTRYW
  152369. 1992a
  152370. GABRIEL WEATHERHEAD
  152371. SULFUR REPORTSC
  152372. S.G. PYNE; SULFOXIMINE, CARBANION, ADDITION TO CARBONYLS, IMINES, ALKYLATION, ASYMMETRIC SYNTHESIS OF OXIRANES, OXETANES, AZIRIDINES, CYCLOPROPANES, REVIEWM
  152373. 7283N
  152374. 2/28/96V,DIASTEREOSELECTIVE REACTIONS OF SULFOXIMINESW
  152375. 1992   12   57
  152376. GABRIEL WEATHERHEAD
  152377. 7284N
  152378. 2/28/96V
  152379. ZUBRICK, JAMES W. THE ORGANIC CHEM LAB SURVIVAL MANUAL: A STUDENT'S GUIDE TO TECHNIQUES, 3RD ED. WILEY: NEW YORK, 1992  A REVIEWa
  152380. GABRIEL WEATHERHEAD
  152381. 7285N
  152382. 2/28/96V
  152383. VOGTLE, F., ET AL. FASCINATING MOLECULES IN ORGANIC CHEMISTRY (TRANSLATED BY G. V. BOYD). WILEY: CHICHESTER, U.K., 1992  A REVIEWa
  152384. GABRIEL WEATHERHEAD
  152385. 7286N
  152386. 2/28/96
  152387. VfVARVOGLIS, ANASTASSIOS. THE ORGANIC CHEMISTRY OF POLYCOORDINATED IODINE. VCH: NEW YORK, 1992  A REVIEWa
  152388. GABRIEL WEATHERHEAD
  152389. 7287N
  152390. 2/28/96V
  152391. RAHMAN, ATTA
  152392. UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 9: STRUCTURE AND CHEMISTRY, PT. B. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1991  A REVIEWa
  152393. GABRIEL WEATHERHEAD
  152394. 7288N
  152395. 2/28/96VXPLUEDDEMANN, EDWIN P. SILANE COUPLING REAGENTS, 2ND ED. PLENUM: NEW YORK, 1991  A REVIEWa
  152396. GABRIEL WEATHERHEAD
  152397. 7289N
  152398. 2/28/96VnPERLMUTTER, P. CONJUGATE ADDITION REACTIONS IN ORGANIC SYNTHESIS. PERGAMON PRESS: OXFORD, U.K., 1992  A REVIEWa
  152399. GABRIEL WEATHERHEAD
  152400. 7290N
  152401. 2/28/96V
  152402. PATAI, SAUL; RAPPOPORT, ZVI, EDS. THE CHEMISTRY OF ALKANES AND CYCLOALKANES (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1992  A REVIEWa
  152403. GABRIEL WEATHERHEAD
  152404. 7291N
  152405. 2/28/96
  152406. VXOSAWA, EIJI; YONEMITSU, OSAMU. CARBOCYCLIC CAGE COMPOUNDS. VCH: NEW YORK, 1992  A REVIEWa
  152407. GABRIEL WEATHERHEAD
  152408. 7292N
  152409. 2/28/96V
  152410. OLAH, GEORGE A.; PRAKASH, G. K. SURYA; CHAMBERS, RICHARD D., EDS. SYNTHETIC FLUORINE CHEMISTRY. WILEY: NEW YORK, 1992  A REVIEWa
  152411. GABRIEL WEATHERHEAD
  152412. 7293N
  152413. 2/28/96VkMILLER, AUDREY. WRITING REACTION MECHANISMS IN ORGANIC CHEMISTRY. ACADEMIC PRESS: SAN DIEGO, 1992  A REVIEWa
  152414. GABRIEL WEATHERHEAD
  152415. 7294N
  152416. 2/28/96VQMARCH, JERRY. ADVANCED ORGANIC CHEMISTRY, 4TH ED. WILEY: NEW YORK, 1992  A REVIEWa
  152417. GABRIEL WEATHERHEAD
  152418. 7295N
  152419. 2/28/96VtLOUPY, A.; TCHOUBAR, B. SALT EFFECTS IN ORGANIC AND ORGANOMETALLIC CHEMISTRY. VCH: WEINHEIM, GERMANY, 1992  A REVIEWa
  152420. GABRIEL WEATHERHEAD
  152421. 7296N
  152422. 2/28/96VuLIJINSKY, WILLIAM. CHEMISTRY AND BIOLOGY OF N
  152423. NITROSO COMPOUNDS. CAMBRIDGE UNIVERSITY PRESS: NEW YORK, 1992  A REVIEWa
  152424. GABRIEL WEATHERHEAD
  152425. 7297N
  152426. 2/28/96V
  152427. JONES, JOHN. AMINO ACID AND PEPTIDE SYNTHESIS (OXFORD CHEMISTRY PRIMERS. 7). OXFORD UNIVERSITY PRESS: OXFORD, U.K., 1992  A REVIEWa
  152428. GABRIEL WEATHERHEAD
  152429. 7298N
  152430. 2/28/96V
  152431. JENKINS, PAUL R. ORGANOMETALLIC REAGENTS IN SYNTHESIS (OXFORD CHEMISTRY PRIMERS. 3). OXFORD UNIVERSITY PRESS: OXFORD, U.K., 1992  A REVIEWa
  152432. GABRIEL WEATHERHEAD
  152433. 7299N
  152434. 2/28/96VFHO, TSE
  152435. LOK. TANDEM ORGANIC REACTIONS. WILEY: NEW YORK, 1992  A REVIEWa
  152436. GABRIEL WEATHERHEAD
  152437. 7300N
  152438. 2/28/96V
  152439. HIRAOKA, MICHIO, ED. CROWN ETHERS AND ANALOGOUS COMPOUNDS (STUDIES IN ORGANIC CHEMISTRY. 45). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1992  A REVIEWa
  152440. GABRIEL WEATHERHEAD
  152441. 7301N
  152442. 2/28/96VaHARWOOD, LAURENCE M., ED. POLAR REARRANGEMENTS. OXFORD UNIVERSITY PRESS: NEW YORK, 1992  A REVIEWa
  152443. GABRIEL WEATHERHEAD
  152444. 7302N
  152445. 2/28/96
  152446. HARTLEY, FRANK R., ED. THE CHEMISTRY OF ORGANOPHOSPHORUS COMPOUNDS, VOL. 2: PHOSPHINE OXIDES, SULFIDES, SELENIDES, AND TELLURIDES (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1992  A REVIEWa
  152447. GABRIEL WEATHERHEAD
  152448. 7303N
  152449. 2/28/96VhHARVEY, RONALD J. POLYCYCLIC AROMATIC HYDROCARBONS. CAMBRIDGE UNIVERSITY PRESS: NEW YORK, 1992  A REVIEWa
  152450. GABRIEL WEATHERHEAD
  152451. 7304N
  152452. 2/28/96VuGUTMAN, IVAN, ED. NUCLEOPHILIC AROMATIC DISPLACEMENT: THE INFLUENCE OF THE NITRO GROUP. VCH: NEW YORK, 1991  A REVIEWa
  152453. GABRIEL WEATHERHEAD
  152454. 7305N
  152455. 2/28/96V
  152456. GRONOWITZ, SALO, ED. THIOPHENE AND ITS DERIVATIVES, PT. 5 (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 44, PT. 5). WILEY: NEW YORK, 1992  A REVIEWa
  152457. GABRIEL WEATHERHEAD
  152458. 7306N
  152459. 2/28/96VSGILCHRIST, T. L. HETEROCYCLIC CHEMISTRY, 2ND ED. WILEY: ESSEX, U.K., 1992  A REVIEWa
  152460. GABRIEL WEATHERHEAD
  152461. 7307N
  152462. 2/28/96
  152463. VWENGEL, ROBERT. HANDBOOK OF ORGANOPHOSPHORUS CHEMISTRY. DEKKER: NEW YORK, 1992  A REVIEWa
  152464. GABRIEL WEATHERHEAD
  152465. 7308N
  152466. 2/28/96VpECKSTEIN, FRITZ, ED. OLIGONUCLEOTIDES AND ANALOGS: A PRACTICAL APPROACH. IRL PRESS: OXFORD, U.K., 1991  A REVIEWa
  152467. GABRIEL WEATHERHEAD
  152468. 7309N
  152469. 2/28/96V
  152470. DAVIES, DAVID T. AROMATIC HETEROCYCLIC CHEMISTRY (OXFORD CHEMISTRY PRIMERS. 2). OXFORD UNIVERSITY PRESS: NEW YORK, 1992  A REVIEWa
  152471. GABRIEL WEATHERHEAD
  152472. 7310N
  152473. 2/28/96V
  152474. ANON. ORGANIC SYNTHESIS IN JAPAN: PAST, PRESENT, AND FUTURE, IN COMMEMORATION OF THE 50TH ANNIVERSARY OF THE SOCIETY OF SYNTHETIC ORGANIC CHEMISTRY, JAPAN. TOKYO KAGAKU DOJIN CO., LTD.: TOKYO, JAPAN, 1992  A REVIEWa
  152475. GABRIEL WEATHERHEAD
  152476. 7311N
  152477. 2/28/96
  152478. SCANLON, THOMAS; SCHULZ, PETER G. RECENT ADVANCES IN CATALYTIC ANTIBODIES ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152479. GABRIEL WEATHERHEAD
  152480. 7312N
  152481. 2/28/96V
  152482. SCOTT, A. IAN. MECHANISTIC ASPECTS OF THE BIOSYNTHESIS OF VITAMIN B12 ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152483. GABRIEL WEATHERHEAD
  152484. 7313N
  152485. 2/28/96V
  152486. WOGGON, WOLF
  152487. DIETRICH;FRETZ,HEINZ. MECHANISM OF CYTOCHROME P
  152488. 450 CATALYZED OXIDATIONS ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152489. GABRIEL WEATHERHEAD
  152490. 7314N
  152491. 2/28/96
  152492.  STREKOWSKI, LUCJAN. MOLECULAR BASIS FOR THE ENHANCEMENT AND INHIBITION OF BELOMYCIN
  152493. MEDIATED DEGRADATION OF DNA BY DNA BINDING COMPOUNDS ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEW
  152494. GABRIEL WEATHERHEAD
  152495. 7315N
  152496. 2/28/96V
  152497. JEFFORD, C. W. NON
  152498. HEME DIOXYGENASES: A UNIFIED MECHANISTIC INTERPRETATION OF THEIR MODE OF ACTION ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152499. GABRIEL WEATHERHEAD
  152500. 7316N
  152501. 2/28/96
  152502. ABELL, ANDERS D. LATENT REACTIVITY: THE STUDY OF ENZYME MECHANISMS AND THE DESIGN OF ENZYME INACTIVATORS ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 2, MECHANISMS OF BIOLOGICAL IMPORTANCE. JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEW
  152503. GABRIEL WEATHERHEAD
  152504. 2/28/96V
  152505. HUA, DUY H. CHIRAL SULFINYLALLYL AND A
  152506. SULFINYL KETIMINE ANIONS IN ORGANIC SYNTHESIS.  ADVANCES IN CARBANION CHEMISTRY. VOLUME 1.  VICTOR SNIECKUS, ED., JAI PRESS: GREENWICH, CT, 1992   A REVIEWa
  152507. GABRIEL WEATHERHEAD
  152508. 7318N
  152509. 2/28/96V
  152510. BRAUN, MANFRED. RECENT DEVELOPMENTS IN STEREOSELECTIVE ALDOL REACTIONS ADVANCES IN CARBANION CHEMISTRY. VOLUME 1.  VICTOR SNIECKUS, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152511. GABRIEL WEATHERHEAD
  152512. 7319N
  152513. 2/28/96V
  152514. BAUER, WALTER; SCHLEYER, PAUL VON RAGUE. RECENT RESULTS IN NMR SPECTROSCOPY OF ORGANOLITHIUM COMPOUNDS.  ADVANCES IN CARBANION CHEMISTRY. VOLUME 1.  VICTOR SNIECKUS, ED., JAI PRESS: GREENWICH, CT, 1992  A REVIEWa
  152515. GABRIEL WEATHERHEAD
  152516. 7320N
  152517. 2/28/96V
  152518. JACKMAN, LLOYD M.; BORTIATYNSKI, JACQUELINE. STRUCTURES OF LITHIUM ENOLATES AND PHENOLATES IN SOLUTION.  ADVANCES IN CARBANION CHEMISTRY. VOLUME 1.  VICTOR SNIECKUS, ED., JAI PRESS: GREENWICH, CT, 1992   A REVIEW
  152519. GABRIEL WEATHERHEAD
  152520. 7321N
  152521. 2/28/96V
  152522. MORDINI, ALESSANDRO. SUPERBASES AND THEIR USE IN ORGANIC SYNTHESIS. ADVANCES IN CARBANION CHEMISTRY. VOLUME 1.  VICTOR SNIECKUS, ED., JAI PRESS: GREENWICH, CT, 1992   A REVIEWa
  152523. GABRIEL WEATHERHEAD
  152524. 7322N
  152525. 2/28/96V
  152526. GREENHILL, JOHN V.; GRAYSHAN, PAUL. THE CEVANE GROUP OF VERATRUM ALKALOIDS THE ALKALOIDS. CHEMISTRY AND PHAMACOLOGY. VOL. 41. A. BROSSI AND G. A. CORDELL, EDS., ACADEMIC PRESS, NEW YORK, 1992  A REVIEWa
  152527. GABRIEL WEATHERHEAD
  152528. 7323N
  152529. 2/28/96V
  152530. BOYE, OLIVIER; BROSSI, ARNOLD. TROPOLONIC COLCHICUM ALKALOIDS AND ALLO CONGENERS THE ALKALOIDS. CHEMISTRY AND PHAMACOLOGY. VOL. 41. A. BROSSI AND G. A. CORDELL, EDS., ACADEMIC PRESS, NEW YORK, 1992  A REVIEWa
  152531. GABRIEL WEATHERHEAD
  152532. 7324N
  152533. 2/28/96
  152534. KOBAYASHI, JUN'ICHI; ISHIBASHI, MASAMI. MARINE ALKALOIDS. II THE ALKALOIDS. CHEMISTRY AND PHAMACOLOGY. VOL. 41. A. BROSSI AND G. A. CORDELL, EDS., ACADEMIC PRESS, NEW YORK, 1992  A REVIEWa
  152535. GABRIEL WEATHERHEAD
  152536. 7325N
  152537. 2/28/96V
  152538. TANTISEWIE, BAMRUNG; RUCHIRAWAT, SOMSAK. ALKALOIDS FROM THE PLANTS OF THAILAND THE ALKALOIDS. CHEMISTRY AND PHAMACOLOGY. VOL. 41. A. BROSSI AND G. A. CORDELL, EDS., ACADEMIC PRESS, NEW YORK, 1992  A REVIEWa
  152539. GABRIEL WEATHERHEAD
  152540. 7326N
  152541. 2/28/96V
  152542. FROST, CHRISTOPHER; HOWARTH, JOSHUA; WILLIAMS, JONATHAN M. J. SELECTIVITY IN PALLADIUM CATALYZED ALLYLIC SUBSTITUTION. 1992, 3(9) 1089
  152543. 1122 TETRAHEDRON: ASYMMETRY  A REVIEWa
  152544. GABRIEL WEATHERHEAD
  152545. 7327N
  152546. 2/28/96V
  152547. WALKER, ANDREW J. ASYMMETRIC CARBON
  152548. CARBON BOND FORMATION USING SULFOXIDE
  152549. STABILIZED CARBANIONS. 1992, 3(8), 961
  152550. 998 TETRAHEDRON: ASYMMETRY  A REVIEWa
  152551. GABRIEL WEATHERHEAD
  152552. 7328N
  152553. 2/28/96
  152554. CARLESS, HOWARD, A. J. THE USE OF CYCLOHEXA
  152555. DIENE
  152556. DIOLS IN ENANTIOSPECIFIC SYNTHESIS. 1992, 3(7), 795
  152557. 826 TETRAHEDRON: ASYMMETRY  A REVIEWa
  152558. GABRIEL WEATHERHEAD
  152559. 7329N
  152560. 2/28/96V
  152561. D'ANGELO, JEAN; DESMAELE, DIDIER; DUMAS, FRANCOISE; GUINGANT, ANDRE. THE ASYMMETRIC MICHAEL ADDITION REACTION USING CHIRAL IMINES. 1992, 3(4), 459
  152562. 505 TETRAHEDRON: ASYMMETRY  A REVIEWa
  152563. GABRIEL WEATHERHEAD
  152564. 7330N
  152565. 2/28/96V
  152566. PETASIS, NICOS A.; PATANE, MICHAEL A. THE SYNTHESIS OF CARBOCYCLIC EIGHT
  152567. MEMBERED RINGS. 1992, 48(28), 5757
  152568. 821 TETRAHEDRON  A REVIEWa
  152569. GABRIEL WEATHERHEAD
  152570. 7331N
  152571. 2/28/96V
  152572. PADWA, ALBERT; KRUMPE, KEITH E. APPLICATION OF INTRAMOLECULAR CARBENOID REACTIONS IN ORGANIC SYNTHESIS. 1992, 48(26), 5385
  152573. 453 TETRAHEDRON  A REVIEWa
  152574. GABRIEL WEATHERHEAD
  152575. 7332N
  152576. 2/28/96VvJUARISTI, EUSEBIO; CUEVAS, GABRIEL. RECENT STUDIES ON THE ANOMERIC EFFECT. 1992, 48(24), 5019
  152577. 87 TETRAHEDRON  A REVIEWa
  152578. GABRIEL WEATHERHEAD
  152579. 7333N
  152580. 2/28/96V
  152581. BURGESS, KEVIN; HENDERSON, IAN. SYNTHETIC APPROACHES TO STEREOISOMERS AND ANALOGS OF CASTANOSPERMINE. 1992, 48(20), 4045
  152582. 66 TETRAHEDRON  A REVIEWa
  152583. GABRIEL WEATHERHEAD
  152584. 7334N
  152585. 2/28/96V
  152586. BRADSHAW, JERALD S.; KRAKOWIAK, KRZYSZTOF E.; IZATT, REED M. PREPARATION OF DIAMINO ETHERS AND POLYAMINES. 1992, 48(22), 4475
  152587. 515 TETRAHEDRON  A REVIEWa
  152588. GABRIEL WEATHERHEAD
  152589. 7335N
  152590. 2/28/96V
  152591. BEAUCAGE, SERGE L.; IYER, RADHAKRISHNAN P. ADVANCES IN THE SYNTHESIS OF OLIGONUCLEOTIDES BY THE PHOSPHORAMIDITE APPROACH. 1992, 48(12), 2223
  152592. 311 TETRAHEDRON  A REVIEWa
  152593. GABRIEL WEATHERHEAD
  152594. 7336N
  152595. 2/28/96VeWARD, R. S. SYNTHESIS OF PODOPHYLLOTOXIN AND RELATED COMPOUNDS. 1992, (8), 719
  152596. 30 SYNTHESIS  A REVIEWa
  152597. GABRIEL WEATHERHEAD
  152598. 7337N
  152599. 2/28/96V
  152600. SINGH, VINOD K. PRACTICAL AND USEFUL METHODS FOR THE ENANTIOSELECTIVE REDUCTION OF UNSYMMETRICAL KETONES. 1992, (7), 607
  152601. 17 SYNTHESIS  A REVIEW
  152602. GABRIEL WEATHERHEAD
  152603. 7338N
  152604. 2/28/96V
  152605. ROSINI, CARLO; FRANZINI, LIVIA; RAFFAELLI, ANDREA; SALVADORI, PIERO. SYNTHESIS AND APPLICATIONS OF BINAPHTHYLIC C2
  152606. SYMMETRY DERIVATIVES AS CHIRAL AUXILIARIES IN ENANTIOSELECTIVE REACTIONS. 1992, (6), 503
  152607. 17 SYNTHESIS  A REVIEWa
  152608. GABRIEL WEATHERHEAD
  152609. 7339N
  152610. 2/28/96VKUEDA, MITSURU. DIRECT POLYCONDENSATION. 1992, (8), 605
  152611. 14 SYNLETT  A REVIEWa
  152612. GABRIEL WEATHERHEAD
  152613. 7340N
  152614. 2/28/96V
  152615. PANDEY, GANESH. SYNTHETIC PERSPECTIVES OF PHOTOINDUCED ELECTRON TRANSFER GENERATED AMINE RADICAL CATIONS. 1992, (7), 546
  152616. 52 SYNLETT  A REVIEWa
  152617. GABRIEL WEATHERHEAD
  152618. 7341N
  152619. 2/28/96V
  152620. TAMAO, KOHEI; KOBAYASHI, KENJI; ITO, YOSHIHIKO. NICKEL(0)
  152621. MEDIATED INTRAMOLECULAR CYCLIZATIONS OF ENYNES, DIENYNES, BIS
  152622. DIENES, AND DIYNES. 1992, (7), 539
  152623. 46 SYNLETT  A REVIEWa
  152624. GABRIEL WEATHERHEAD
  152625. 7342N
  152626. 2/28/96
  152627. REGER, DANIEL L. POLY(PYRAZOLYL)BORATE COMPLEXES OF TIN(II) AND LEAD(II). THE QUEST FOR A COORDINATION COMPLEX WITH A STEREOCHEMICALLY INACTIVE LONE PAIR. 1992, (6), 469
  152628. 75 SYNLETT  A REVIEWa
  152629. GABRIEL WEATHERHEAD
  152630. 7343N
  152631. 2/28/96V
  152632. SATOH, TSUYOSHI; YAMAKAWA, KOJI. RECENT DEVELOPMENTS IN ORGANIC SYNTHESIS WITH 1
  152633. HALOALKYL ARYL SULFOXIDES. 1992, (6), 455
  152634. 68 SYNLETT  A REVIEWa
  152635. GABRIEL WEATHERHEAD
  152636. 7344N
  152637. 2/28/96V
  152638. KNOELKER, HANS JOACHIM. IRON
  152639. MEDIATED SYNTHESIS OF HETEROCYCLIC RING SYSTEMS AND APPLICATIONS IN ALKALOID CHEMISTRY. 1992, (5), 371
  152640. 87 SYNLETT  A REVIEWa
  152641. GABRIEL WEATHERHEAD
  152642. 7345N
  152643. 2/28/96V
  152644. MATHEY, FRANCOIS; MARINETTI, ANGELA; MERCIER, FRANCOIS. SYNTHESIS OF ORGANOPHOSPHORUS COMPOUNDS VIA THE COORDINATION SPHERES OF TRANSITION METALS: SOME NONCLASSICAL EXAMPLES. 1992, (5), 363
  152645. 70 SYNLETT  A REVIEWa
  152646. GABRIEL WEATHERHEAD
  152647. 7346N
  152648. 2/28/96
  152649. 6VpDZHAFAROV, M. K. RETRO
  152650. ALDOL PROCESSES IN STEROID CHEMISTRY. 1992, 61(3), 363 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152651. GABRIEL WEATHERHEAD
  152652. 7347N
  152653. 2/28/96V
  152654. NIKONOV, G. N.; BALYEVA, A. S. COMPOUNDS CONTAINING PHOSPHORUS AND BORON. 1992, 61(3), 335
  152655. 351 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152656. GABRIEL WEATHERHEAD
  152657. 7348N
  152658. 2/28/96V
  152659. KHASKIN, B. A.; MOLODOVA, O. D.; TORGASHEVA, N. A. REACTIONS OF PHOSPHORUS
  152660. CONTAINING COMPOUNDS WITH DIAZO COMPOUNDS AND CARBENES. 1992, 61(3), 306
  152661. 334 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152662. GABRIEL WEATHERHEAD
  152663. 7349N
  152664. 2/28/96VsVOVK, M. V.; SAMARAI, L. I. N
  152665. FUNCTIONALIZED CARBODIIMIDES. 1992, 61(3), 297
  152666. 305 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152667. GABRIEL WEATHERHEAD
  152668. 7350N
  152669. 2/28/96VvNEFEDOV, V. D.; SINOTOVA, E. N.; LEBEDEV, V. P. VINYL CATIONS. 1992, 61(3), 283
  152670. 296 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152671. GABRIEL WEATHERHEAD
  152672. 7351N
  152673. 2/28/96
  152674. LAKHVICH, F. A.; PASHKOVSKII, F. S.; KOROLEVA, E. V. HETEROPROSTANOIDS: SYNTHESIS AND BIOLOGICAL ACTIVITY. 1992,61(2),243 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152675. GABRIEL WEATHERHEAD
  152676. 7352N
  152677. 2/28/96V
  152678. BEL'SKII, F. I.; POLIKARPOV, YU. M.; KABACHNIK, M. I. CYCLOPENDANT LIGANDS. 1992, 61(2), 221
  152679. 242 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152680. GABRIEL WEATHERHEAD
  152681. 7353N
  152682. 2/28/96V
  152683. STARTSEV, A. N. MECHANISM OF THE HYDROGENOLYSIS OF THIOPHENE ON BIMETALLIC SULPHIDE CATALYSTS. 1992, 61(2), 175
  152684. 87 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152685. GABRIEL WEATHERHEAD
  152686. 7354N
  152687. 2/28/96V
  152688. SEMIKOLENOV, V. A. MODERN APPROACHES TO THE PREPARATION OF "PALLADIUM ON CHARCOAL" CATALYSTS. 1992, 61(2),168
  152689. 74 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152690. GABRIEL WEATHERHEAD
  152691. 7355N
  152692. 2/28/96V
  152693. GERASIMOV, O. V.; PARMON, V. N. PHOTOCATALYSIS BY TRANSITION METAL COMPLEXES. 1992, 61(2),154
  152694. 67 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152695. GABRIEL WEATHERHEAD
  152696. 7356N
  152697. 2/28/96V
  152698. SHEVCHENKO, S. M.; APUSHKINSKII, A. G. QUINONE METHIDES IN THE CHEMISTRY OF WOOD. 1992, 61(1),105 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152699. GABRIEL WEATHERHEAD
  152700. 7357N
  152701. 2/28/96V
  152702. DEEV, L. E.; NAZARENKO, T. I.; PASHKEVICH, K. I.; PONOMAREV,V. G. IODOPERFLUOROALKANES. 1992,61(1),4054 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152703. GABRIEL WEATHERHEAD
  152704. 7358N
  152705. 2/28/96V
  152706. BUDYKA, M. F.; KANTOR, M. M.; ALFIMOV, M. V. PHOTOCHEMISTRY OF PHENYL AZIDE. 1992, 61(1), 25
  152707. 39 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152708. GABRIEL WEATHERHEAD
  152709. 7359N
  152710. 2/28/96V
  152711. ARUTYUNOV, V. S.; VEDENEEV, V. I. PYROLYSIS OF METHANE IN THE TEMPERATURE RANGE 100 1700 K. 1991, 60(12),1384
  152712. 97 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152713. GABRIEL WEATHERHEAD
  152714. 7360N
  152715. 2/28/96V
  152716. KUROYAN, R. A. SYNTHESIS OF SPIRONE
  152717. [PIPERIDINE4,C'N
  152718. HETERO(CARBO)CYCLES]. 1991,60(12),1368
  152719. 83 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152720. GABRIEL WEATHERHEAD
  152721. 7361N
  152722. 2/28/96V
  152723. TROFIMOV, B. A.; RAKHMATULINA, T. N.; GUSAROVA, N. K.; MALYSHEVA, S. ELEMENTAL PHOSPHORUS
  152724. STRONG BASE AS A SYSTEM FOR THE SYNTHESIS OF ORGANOPHOSPHORUS COMPOUNDS 1991,60(12),1360
  152725. 67 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152726. GABRIEL WEATHERHEAD
  152727. 7362N
  152728. 2/28/96V
  152729. ABALONIN, B. E. INVESTIGATIONS ON THE ARBUZOV AND RETRO
  152730. ARBUZOV REACTIONS AMONG THE ORGANIC DERIVATIVES OF ARSENIC. 1991, 60(12), 1346
  152731. 59 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152732. GABRIEL WEATHERHEAD
  152733. 7363N
  152734. 2/28/96V
  152735. RYBAKOVA, I. A.; PRILEZHAEVA, E. N.; LITVINOV, V. P. METHODS OF REPLACING HALOGEN IN AROMATIC COMPOUNDS BY RS
  152736. FUNCTIONS. 1991, 60(12), 1331
  152737. 45 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152738. GABRIEL WEATHERHEAD
  152739. 7364N
  152740. 2/28/96V
  152741. GUKASYAN, A. O.; GALSTYAN, L. KH; AVETISYAN, A. A. SYNTHESIS, STRUCTURE, AND REACTIVITY OF A
  152742. (TRIHALOMETHYL)CARBINOLS. 1991, 60(12), 1318
  152743. 30 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152744. GABRIEL WEATHERHEAD
  152745. 2/28/96VzUL'EV, M. V.; SHTEFAN, E. D.; VVEDENSKII, V. YU. THIOPHENETHIOLS. 1991, 60(12), 1309
  152746. 17 RUSSIAN CHEMICAL REVIEWS  A REVIEWa
  152747. GABRIEL WEATHERHEAD
  152748. 7366N
  152749. 2/28/96V
  152750. WONG, CHI HUEY; LIU, KEVIN K. C.; KAJIMOTO, TETSUYA; CHEN, LIHREN; ZHONG, ZIYANG; DUMAS, DAVID P.; LIU, JENNIFER L. C.; ET AL. ENZYMES FOR CARBOHYDRATE AND PEPTIDE SYNTHESES. 1992, 64(8),1197
  152751. 202 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152752. GABRIEL WEATHERHEAD
  152753. 7367N
  152754. 2/28/96V
  152755. VARFOLOMEEV, S. D.; RAININA, E. I.; LOZINSKII, V. I. CRYOIMMOBILIZED ENZYMES AND CELLS IN ORGANIC SYNTHESIS. 1992, 64(8), 1193
  152756. 6 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152757. GABRIEL WEATHERHEAD
  152758. 7368N
  152759. 2/28/96V
  152760. TAMM, CHRISTOPH. PIG LIVER ESTERASE CATALYZED HYDROLYSIS: SUBSTRATE SPECIFICITY AND STEREOSELECTIVITY. 1992, 64(8), 1187
  152761. 91 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152762. GABRIEL WEATHERHEAD
  152763. 7369N
  152764. 2/28/96
  152765. SHINKAI, I.; BHUPATHY, M. CHEMOENZYMIC SYNTHESIS OF A NOVEL LTD4 ANTAGONIST. 1992, 64(8),1177
  152766. 80 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152767. GABRIEL WEATHERHEAD
  152768. 7370N
  152769. 2/28/96V
  152770. ROBERTS, S. M. EXPLOITATION OF MICROBIOLOGICAL METHODS FOR THE SYNTHESIS OF BIOLOGICALLY ACTIVE NATURAL PRODUCTS AND ANALOGS. 1992, 64(8),1153
  152771. 5 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152772. GABRIEL WEATHERHEAD
  152773. 7371N
  152774. 2/28/96V
  152775. RAO, K. RAMA. NEW TRENDS IN BIOCATALYSIS IN THE PRESENCE OF CYCLODEXTRINS. 1992, 64(8),1141
  152776. 5 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152777. GABRIEL WEATHERHEAD
  152778. 7372N
  152779. 2/28/96V
  152780. PARMAR, V. S.; PRASAD, A. K.; B ISHT, K. S.; SINHA, RITA; TANEJA, POONAM. POTENTIAL APPLICATIONS OF ENZYME
  152781. MEDIATED TRANSESTERIFICATIONS IN THE SYNTHESIS OF BIOACTIVE COMPOUNDS. 1992, 64(8),1135
  152782. 9 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152783. GABRIEL WEATHERHEAD
  152784. 7373N
  152785. 2/28/96
  152786. HULT, KARL; NORIN, TORBJOERN. ENANTIOSELECTIVITY OF SOME LIPASES: CONTROL AND PREDICTION. 1992,64(8),112934 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152787. GABRIEL WEATHERHEAD
  152788. 7374N
  152789. 2/28/96V
  152790. JOHNSON, CARL R.; ADAMS, JOSEPH P.; BIS, SCOTT J.; DE JONG, RANDALL L.; GOLEBIOWSKI, ADAM; MEDICH, JOHN R.; PENNING, THOMAS D.; ET AL. APPLICATIONS OF ENZYMES IN THE SYNTHESIS OF BIOACTIVE POLYOLS. 1992, 64(8),111520 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152791. GABRIEL WEATHERHEAD
  152792. 7375N
  152793. 2/28/96V
  152794. HUDLICKY, TOMAS; FAN, RULIN; LUNA, HECTOR; OLIVO, HORACIO; PRICE, JOHN. ENZYMIC HYDROXYLATION OF ARENE AND SYMMETRY CONSIDERATIONS IN EFFICIENT SYNTHETIC DESIGN OF OXYGENATED NATURAL PRODUCTS. 1992, 64(8),1109
  152795. 13 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152796. GABRIEL WEATHERHEAD
  152797. 7376N
  152798. 2/28/96V]HILVERT, DONALD. ANTIBODY CATALYSIS. 1992, 64(8), 1103
  152799. 8 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152800. GABRIEL WEATHERHEAD
  152801. 7377N
  152802. 2/28/96
  152803. FRONZA, GIOVANNI; FUGANTI, CLAUDIO; GRASSELLI, PIERO; PEDROCCHI, FANTONI GIUSEPPE; SERVI, STEFANO. MINOR SYNTHETIC CAPACITIES OF BAKERS' YEAST TOWARDS UNNATURAL SUBSTRATES. 1992, 64(8), 1099
  152804. 101 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152805. GABRIEL WEATHERHEAD
  152806. 7378N
  152807. 2/28/96V
  152808. FRANSSEN, M. C. R.; BOAVIDA, DOS SANTOS P. M. A. C.; CAMACHO, MONDRIL N. L. F. L.; DE GROOT, A. ENZYMIC SYNTHESIS OF A CHIRAL BUILDING BLOCK FOR PERHYDROFURO[2,3B]FURANS. 1992, 64(8), 1089
  152809. 92 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152810. GABRIEL WEATHERHEAD
  152811. 7379N
  152812. 2/28/96V
  152813. BERGER, BRIGITTE; DE RAADT, ANNA; GRIENGL, HERFRIED; HAYDEN, WALTER; HECHTBERGER, PETRA; KLEMPIER, NORBERT; FABER, KURT. USEFUL HYDROLYTIC ENZYMES: PROTEASES, LIPASES AND NITRILASES. 1992, 64(8),1085
  152814. 8 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152815. GABRIEL WEATHERHEAD
  152816. 7380N
  152817. 2/28/96
  152818. ALBRIGHT, T. A.; HALEVI, E. A. GUIDELINES FOR THE PRESENTATION OF QUANTUM MECHANICAL COMPUTATIONAL DATA IN ORGANIC CHEMISTRY. 1992, 64(8),1203
  152819. 9 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152820. GABRIEL WEATHERHEAD
  152821. 7381N
  152822. 2/28/96V
  152823. ADER, U.; ANDERSCH, P.; BERGER, M.; GOERGENS, U.; SEEMAYER, R.; SCHNEIDER, M. HYDROLASES IN ORGANIC SYNTHESIS: PREPARATION OF ENANTIOMERICALLY PURE COMPOUNDS. 1992, 64(8),1165
  152824. 70 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152825. GABRIEL WEATHERHEAD
  152826. 7382N
  152827. 2/28/96V
  152828. DRENTH, W. GUIDELINES FOR THE PUBLICATION OF RESEARCH IN EXPERIMENTAL ORGANIC CHEMISTRY. 1992, 64(7), 989
  152829. 90 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152830. GABRIEL WEATHERHEAD
  152831. 7383N
  152832. 2/28/96V
  152833. LEBEDEV, YA S.; RAKHIMOV, R. R.; PROKOF'EV, A. I.; BREZGUNOV, A. YU. FAST MOLECULAR DYNAMICS: NOVEL EFFECTS STUDIED BY 3 CM AND 2 MM BAND EPR. 1992, 64(6), 87381 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152834. GABRIEL WEATHERHEAD
  152835. 7384N
  152836. 2/28/96
  152837. ICHIKAWA, TSUNEKI. APPLICATION OF ESE SPECTROSCOPY TO THE STUDY OF RADICAL REACTIONS IN SOLIDS. 1992, 64(6), 841
  152838. 6 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152839. GABRIEL WEATHERHEAD
  152840. 7385N
  152841. 2/28/96V
  152842. GROENEN, E. J. J.; KOK, P.; ROS, M. FROM POLYENALS TO RETINAL: AN ELECTRON
  152843. ECHO STUDY OF THE TRIPLET STATE. 1992, 64(6), 833
  152844. 9 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152845. GABRIEL WEATHERHEAD
  152846. 7386N
  152847. 2/28/96V
  152848. HAYASHI, TAMIO; KUBO, AKIHIKO; OZAWA, FUMIYUKI. CATALYTIC ASYMMETRIC ARYLATION OF OLEFINS. 1992, 64(3), 4217 PURE AND APPLIED CHEMISTRY  A REVIEWa
  152849. GABRIEL WEATHERHEAD
  152850. 7387N
  152851. 2/28/96V
  152852. VAN, LOON J. D.; VERBOOM, W.; REINHOUDT, D. N. SELECTIVE FUNCTIONALIZATION AND CONFORMATIONAL PROPERTIES OF CALIX[4]ARENES. 1992, 24(4), 437
  152853. 62 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152854. GABRIEL WEATHERHEAD
  152855. 7388N
  152856. 2/28/96
  152857. MARTIN, ROBERT. USES OF THE FRIES REARRANGEMENT FOR THE PREPARATION OF HYDROXYARYL KETONES. 1992, 24(4), 369
  152858. 435 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152859. GABRIEL WEATHERHEAD
  152860. 7389N
  152861. 2/28/96V
  152862. MOUTET, JEAN CLAUDE. ELECTROCATALYTIC HYDROGENATION ON HYDROGEN
  152863. ACTIVE ELECTRODES. 1992, 24(3), 30925 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152864. GABRIEL WEATHERHEAD
  152865. 7390N
  152866. 2/28/96V
  152867. GALLI, CARLO. "CESIUM ION EFFECT" AND MACROCYCLIZATION. 1992, 24(3), 285
  152868. 307 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152869. GABRIEL WEATHERHEAD
  152870. 7391N
  152871. 2/28/96V
  152872. TAYLOR, STEPHEN K. BIOSYNTHETIC, BIOMIMETIC AND RELATED EPOXIDE CYCLIZATIONS. 1992, 24(3), 245 84 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152873. GABRIEL WEATHERHEAD
  152874. 7392N
  152875. 2/28/96
  152876. EGUCHI, SHOJI; MATSUSHITA, YUJI; YAMASHITA, KEIZO. THE AZA
  152877. WITTIG REACTION IN HETEROCYCLIC SYNTHESIS. 1992, 24(2),209
  152878. 243 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  A REVIEWa
  152879. GABRIEL WEATHERHEAD
  152880. 7393N
  152881. 2/28/96V[ROBINS, D. J. PYRROLIZIDINE ALKALOIDS. 1992, 9(4), 313
  152882. 21 NATURAL PRODUCT REPORTS  A REVIEWa
  152883. GABRIEL WEATHERHEAD
  152884. 7394N
  152885. 2/28/96VeMERRITT, A. T.; LEY, S. V. CLERODANE DITERPENOIDS. 1992,9(3),243
  152886. 87 NATURAL PRODUCT REPORTS  A REVIEWa
  152887. GABRIEL WEATHERHEAD
  152888. 7395N
  152889. 2/28/96V[FRAGA, B. M. NATURAL SESQUITERPENOIDS. 1992, 9(3), 217
  152890. 41 NATURAL PRODUCT REPORTS  A REVIEWa
  152891. GABRIEL WEATHERHEAD
  152892. 7396N
  152893. 2/28/96V
  152894. BUGG, T. D. H.; WALSH, C. T. INTRACELLULAR STEPS OF BACTERIAL CELL WALL PEPTIDOGLYCAN BIOSYNTHESIS: ENZYMOLOGY, ANTIBIOTICS, AND ANTIBIOTIC RESISTANCE. 1992, 9(3),199
  152895. 215 NATURAL PRODUCT REPORTS  A REVIEWa
  152896. GABRIEL WEATHERHEAD
  152897. 7397N
  152898. 2/28/96
  152899. CROMBIE, L. NATURAL PRODUCTS AND THE SESQUICENTENARY OF THE ROYAL SOCIETY OF CHEMISTRY: SOME RANDOM COMMENTS. 1992, 9(3), 193
  152900. 8 NATURAL PRODUCT REPORTS  A REVIEWa
  152901. GABRIEL WEATHERHEAD
  152902. 7398N
  152903. 2/28/96VkROHR, J.; THIERICKE, R. ANGUCYCLINE GROUP ANTIBIOTICS. 1992, 9(2), 103
  152904. 37 NATURAL PRODUCT REPORTS  A REVIEWa
  152905. GABRIEL WEATHERHEAD
  152906. 7399N
  152907. 2/28/96VxGRIFFITHS, WILLIAM P. RUTHENIUM OXO COMPLEXES AS ORGANIC OXIDANTS. 1992, 21(3),179
  152908. 85 CHEMICAL SOCIETY REVIEWS  A REVIEWa
  152909. GABRIEL WEATHERHEAD
  152910. 7400N
  152911. 2/28/96V
  152912. REICHARDT, C. SOLVATOCHROMISM, THERMOCHROMISM, PIEZOCHROMISM, HALOCHROMISM, AND CHIRO
  152913. SOLVATOCHROMISM OF PYRIDINIUM N
  152914. PHENOXIDE BETAINE DYES. 1992, 21(3),14753 CHEMICAL SOCIETY REVIEWS  A REVIEWa
  152915. GABRIEL WEATHERHEAD
  152916. 7401N
  152917. 2/28/96
  152918. O'HARE, D. STRUCTURE, DYNAMICS, AND ELECTRONIC PROPERTIES OF COBALTOCENE IN TIN SULFIDE SELENIDE (SNS2
  152919. XSEX) {0 
  152920.  2}. 1992,21(2),121
  152921. 6 CHEMICAL SOCIETY REVIEWS  A REVIEWa
  152922. GABRIEL WEATHERHEAD
  152923. 7402N
  152924. 2/28/96VZWALTON, JOHN C. BRIDGEHEAD RADICALS. 1992,21(2), 105
  152925. 12 CHEMICAL SOCIETY REVIEWS  A REVIEWa
  152926. GABRIEL WEATHERHEAD
  152927. 7403N
  152928. 2/28/96V
  152929. LI, SONG; PURDY, WILLIAM C. CYCLODEXTRINS AND THEIR APPLICATIONS IN ANALYTICAL CHEMISTRY. 1992, 92(6),145770 CHEMICAL REVIEWS  A REVIEWa
  152930. GABRIEL WEATHERHEAD
  152931. 7404N
  152932. 2/28/96V
  152933. MEUNIER, BERNARD. METALLOPORPHYRINS AS VERSATILE CATALYSTS FOR OXIDATION REACTIONS AND OXIDATIVE DNA CLEAVAGE. 1992, 92(6), 1411
  152934. 56 CHEMICAL REVIEWS  A REVIEWa
  152935. GABRIEL WEATHERHEAD
  152936. 7405N
  152937. 2/28/96
  152938. IZATT, REED M.; BRADSHAW, JERALD S.; PAWLAK, KRYSTYNA; BRUENING, RONALD L.; TARBET, BRYON J. THERMODYNAMIC AND KINETIC DATA FOR MACROCYCLE INTERACTION WITH NEUTRAL MOLECULES. 1992, 92(6),1261
  152939. 354 CHEMICAL REVIEWS  A REVIEWa
  152940. GABRIEL WEATHERHEAD
  152941. 7406N
  152942. 2/28/96VoSEITZ, GUNTHER; IMMING, PETER. OXOCARBONS AND PSEUDOOXOCARBONS. 1992, 92(6), 1227
  152943. 60 CHEMICAL REVIEWS  A REVIEWa
  152944. GABRIEL WEATHERHEAD
  152945. 7407N
  152946. 2/28/96V
  152947. BANOUB, JOSEPH; BOULLANGER, PAUL; LAFONT, DOMINIQUE. SYNTHESIS OF OLIGOSACCHARIDES OF 2
  152948. AMINO
  152949. DEOXY SUGARS. 1992, 92(6), 1167
  152950. 95. CHEMICAL REVIEWS  A REVIEWa
  152951. GABRIEL WEATHERHEAD
  152952. 7408N
  152953. 2/28/96V
  152954. LOUPY, ANDRE; TCHOUBAR, BIANKA; ASTRUC, DIDIER. SALT EFFECTS RESULTING FROM EXCHANGE BETWEEN TWO ION
  152955. PAIRS AND THEIR CRITICAL ROLE ON REACTION PATHWAYS. 1992, 92(6), 1141
  152956. 1165 CHEMICAL REVIEWS  A REVIEWa
  152957. GABRIEL WEATHERHEAD
  152958. 7409N
  152959. 2/28/96
  152960. SANTANIELLO, ENZO; FERRABOSCHI, PATRIZIA; GRISENTI, PARIDE; MANZOCCHI, ADA. THE BIOCATALYTIC APPROACH TO THE PREPARATION OF ENANTIOMERICALLY PURE CHIRAL BUILDING BLOCKS. 1992, 92(5), 1071
  152961. 140 CHEMICAL REVIEWS  A REVIEWa
  152962. GABRIEL WEATHERHEAD
  152963. 7410N
  152964. 2/28/96V
  152965. ZASSINOVICH, GRAZIA; MESTRONI, GIOVANNI; GLADIALI, SERAFINO. ASYMMETRIC HYDROGEN TRANSFER REACTIONS PROMOTED BY HOMOGENEOUS TRANSITION METAL CATALYSTS. 1992, 92(5), 1051
  152966. 69 CHEMICAL REVIEWS  A REVIEWa
  152967. GABRIEL WEATHERHEAD
  152968. 7411N
  152969. 2/28/96V~MIKAMI, KOICHI; SHIMIZU, MASAKI. ASYMMETRIC ENE REACTIONS IN ORGANIC SYNTHESIS. 1992, 92(5),1021
  152970. 50 CHEMICAL REVIEWS  A REVIEWa
  152971. GABRIEL WEATHERHEAD
  152972. 7412N
  152973. 2/28/96V{KAGAN, HENRI B.; RIANT, OLIVIER. CATALYTIC ASYMMETRIC DIELS
  152974. ALDER REACTIONS. 1992, 92(5),1007
  152975. 19 CHEMICAL REVIEWS  A REVIEWa
  152976. GABRIEL WEATHERHEAD
  152977. 7413N
  152978. 2/28/96
  152979. yV}CHAN, T. H.; WANG, D. CHIRAL ORGANOSILICON COMPOUNDS IN ASYMMETRIC SYNTHESIS. 1992, 92(5), 9951006 CHEMICAL REVIEWS  A REVIEWa
  152980. GABRIEL WEATHERHEAD
  152981. 7414N
  152982. 2/28/96VUWHITESELL, JAMES K. CYCLOHEXYL
  152983. BASED CHIRAL AUXILIARIES 1992, 92(5), 953
  152984. 64  A REVIEWa
  152985. GABRIEL WEATHERHEAD
  152986. 7415N
  152987. 2/28/96V
  152988. BLASER, HANS
  152989. ULRICH. THE CHIRAL POOL AS A SOURCE OF ENANTIOSELECTIVE CATALYSTS AND AUXILIARIES. 1992, 92(5), 93552 CHEMICAL REVIEWS  A REVIEWa
  152990. GABRIEL WEATHERHEAD
  152991. 7416N
  152992. 2/28/96V
  152993. DAVIS, FRANKLIN A.; CHEN, BANG
  152994. CHI. ASYMMETRIC HYDROXYLATION OF ENOLATES WITH N
  152995. SULFONYLOXAZIRIDINES. 1992, 92(5), 919
  152996. 34 CHEMICAL REVIEWS  A REVIEWa
  152997. GABRIEL WEATHERHEAD
  152998. 7417N
  152999. 2/28/96V|WILLIAMS, ROBERT M.; HENDRIX, JAMES A. ASYMMETRIC SYNTHESIS OF ARYLGLYCINES. 1992, 92(5), 889
  153000. 917 CHEMICAL REVIEWS  A REVIEWa
  153001. GABRIEL WEATHERHEAD
  153002. 7418N
  153003. 2/28/96
  153004. SCHURIG, VOLKER; BETSCHINGER, FRANK. METAL
  153005. MEDIATED ENANTIOSELECTIVE ACCESS TO UNFUNCTIONALIZED ALIPHATIC OXIRANES: PROCHIRAL AND CHIRAL RECOGNITION. 1992, 92(5), 873
  153006. 88 CHEMICAL REVIEWS  A REVIEWa
  153007. GABRIEL WEATHERHEAD
  153008. 7419N
  153009. 2/28/96V
  153010. SAWAMURA, MASAYA; ITO, YOSHIHIKO. CATALYTIC ASYMMETRIC SYNTHESIS BY MEANS OF SECONDARY INTERACTION BETWEEN CHIRAL LIGANDS AND SUBSTRATES. 1992, 92(5), 85771 CHEMICAL REVIEWS  A REVIEWa
  153011. GABRIEL WEATHERHEAD
  153012. 7420N
  153013. 2/28/96V
  153014. SOAI, KENSO; NIWA, SEIJI. ENANTIOSELECTIVE ADDITION OF ORGANOZINC REAGENTS TO ALDEHYDES. 1992, 92(5), 833
  153015. 56 CHEMICAL REVIEWS  A REVIEWa
  153016. GABRIEL WEATHERHEAD
  153017. 7421N
  153018. 2/28/96V
  153019. DUTHALER, RUDOLF O.; HAFNER, ANDREAS. CHIRAL TITANIUM COMPLEXES FOR ENANTIOSELECTIVE ADDITION OF NUCLEOPHILES TO CARBONYL GROUPS. 1992, 92(5), 807
  153020. 32 CHEMICAL REVIEWS  A REVIEWa
  153021. GABRIEL WEATHERHEAD
  153022. 7422N
  153023. 2/28/96
  153024. VuROSSITER, BRYANTE.; SWINGLE, NICOLE M. ASYMMETRIC CONJUGATE ADDITION. 1992, 92(5), 771
  153025. 806 CHEMICAL REVIEWS  A REVIEWa
  153026. GABRIEL WEATHERHEAD
  153027. 7423N
  153028. 2/28/96VpINOUE, YOSHIHISA. ASYMMETRIC PHOTOCHEMICAL REACTIONS IN SOLUTION. 1992, 92(5), 741
  153029. 70 CHEMICAL REVIEWS  A REVIEWa
  153030. GABRIEL WEATHERHEAD
  153031. 7424N
  153032. 2/28/96V
  153033. WALLINGTON, T. J.; DAGAUT, P.; KURYLO, M. J. UV ABSORPTION CROSS SECTIONS AND REACTION KINETICS AND MECHANISMS FOR PEROXY RADICALS IN THE GAS PHASE. 1992, 92(4), 667
  153034. 710 CHEMICAL REVIEWS  A REVIEWa
  153035. GABRIEL WEATHERHEAD
  153036. 7425N
  153037. 2/28/96V
  153038. BRUNNER, HENRI. ENANTIOSELECTIVE RHODIUM(II) CATALYSTS. 1992, 31(9), 1183
  153039. 5 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153040. GABRIEL WEATHERHEAD
  153041. 7426N
  153042. 2/28/96
  153043. PATERSON, IAN; BERRISFORD, DAVID J. MESO
  153044. EPOXIDES IN ASYMMETRIC SYNTHESIS: ENANTIOSELECTIVE OPENING BY NUCLEOPHILES IN THE PRESENCE OF CHIRAL LEWIS ACIDS. 1992, 31(9), 1179
  153045. 80 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153046. GABRIEL WEATHERHEAD
  153047. 7427N
  153048. 2/28/96V
  153049. BUDA, ANDRZEJ B.; AUF DER HEYDE, THOMAS; MISLOW, KURT. ON QUANTIFYING CHIRALITY. 1992, 31(8), 989
  153050. 1007 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153051. GABRIEL WEATHERHEAD
  153052. 7428N
  153053. 2/28/96V
  153054. HOPF, HENNING; MAAS, GERHARD. PREPARATION AND PROPERTIES, REACTIONS AND APPLICATIONS OF RADIALENES. 1992, 31(8), 931
  153055. 54 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153056. GABRIEL WEATHERHEAD
  153057. 7429N
  153058. 2/28/96V
  153059. STODDART, J. FRASER. CYCLODEXTRINS: OFF
  153060. SHELF COMPONENTS FOR THE CONSTRUCTION OF MECHANICALLY INTERLOCKED MOLECULAR SYSTEMS. 1992, 31(7), 846
  153061. 8 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153062. GABRIEL WEATHERHEAD
  153063. 7430N
  153064. 2/28/96V
  153065. BOCHE, GERNOT. PENETRATED ION PAIRS: A NEW FORM OF ION PAIR. 1992, 31(6), 731
  153066. 2 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153067. GABRIEL WEATHERHEAD
  153068. 7431N
  153069. 2/28/96V
  153070. LOHRAY, BRAJ B.; BHUSHAN, VIDYA. OXAZABOROLIDINES AND DIOXABOROLIDINES IN ENANTIOSELECTIVE CATALYSIS. 1992, 31(6), 729
  153071. 30 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153072. GABRIEL WEATHERHEAD
  153073. 7432N
  153074. 2/28/96V
  153075. HOUK, KENDALL, N.; LI, YI; EVANSECK, JEFFREY D. TRANSITON STRUCTURES OF HYDROCARBON PERICYCLIC REACTIONS. 1992, 31(6), 682
  153076. 708 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153077. GABRIEL WEATHERHEAD
  153078. 7433N
  153079. 2/28/96V
  153080. HEATHCOCK, CLAYTON H. THE ENCHANTING ALKALOIDS OF YUZURIHA. 1992, 31(6), 665
  153081. 81 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153082. GABRIEL WEATHERHEAD
  153083. 7434N
  153084. 2/28/96
  153085. BOCK, HANS; RUPPERT, KLAUS; NATHER, CHRISTIAN; HAVLAS, ZDENEK; HERRMANN, HANS
  153086. FRIEDRICH; ARAD, CLAUDIA; GOBEL, AIKA; JOHN, ANDREAS; MEURET, JOCHEN; NICK, SABINE; RAUSCHENBACH, ANDREAS; SEITZ, WOLFGANG; VAUPEL, TORSTEN; SOLOUKI, BAHMAN. STRUCTURE OF CHARGE
  153087. PERTURBED STERICALLY OVERCROWDED MOLECULES. 20. DISTORTED MOLECULES: PERTURBATION DESIGN, PREPARATION AND STRUCTURES. 1992, 31(5), 550
  153088. 81 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEW
  153089. GABRIEL WEATHERHEAD
  153090. 7435N
  153091. 2/28/96V
  153092. SEEL, CHRISTIAN; VOGTLE, FRITZ. MOLECULES WITH LARGE CAVITIES IN SUPRAMOLECULAR CHEMISTRY. 1992, 31(5), 52 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  A REVIEWa
  153093. GABRIEL WEATHERHEAD
  153094. 7436N
  153095. 2/28/96V
  153096. FU, XIAOYONG; COOK, JAMES M. THE SYNTHESIS OF POLYQUINANES AND POLYQUINENES VIA THE WEISS REACTION. 1992,25(2),43
  153097. 55 ALDRICHIMICA ACTA  A REVIEWa
  153098. GABRIEL WEATHERHEAD
  153099. 7437N
  153100. 2/28/96
  153101. NEWKOME, GEORGE R.; MOOREFIELD, CHARLES N.; BAKER, GREGORY R. .BUILDING BLOCKS FOR DENDRITIC MACROMOLECULES. 1992,25(2),31
  153102. 38 ALDRICHIMICA ACTA  A REVIEWa
  153103. GABRIEL WEATHERHEAD
  153104. 7438N
  153105. 2/28/96VrWILLIAMS, ROBERT M. ASYMMETRIC SYNTHESES OF ALPHA
  153106. AMINO ACIDS. 1992, 24(1),11
  153107. 13,15
  153108. 25 ALDRICHIMICA ACTA  A REVIEWa
  153109. GABRIEL WEATHERHEAD
  153110. 7439N
  153111. 2/28/96VHABELES, ROBERT H. A METHIONINE SALVAGE PATHWAY. 1992,25(1),3
  153112. 7  A REVIEWa
  153113. GABRIEL WEATHERHEAD
  153114. 7440N
  153115. 2/28/96V
  153116. MCGLINCHEY, MICHAEL J. SLOWED TRIPODAL ROTATION IN ARENE
  153117. CHROMIUM COMPLEXES: STERIC AND ELECTRONIC BARRIERS. 1992, 34, 285
  153118. 326 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153119. GABRIEL WEATHERHEAD
  153120. 7441N
  153121. 2/28/96V
  153122. FALCK, PHILLIPE; MONTEIL, FANNY. USE OF WATER
  153123. SOLUBLE LIGANDS IN HOMOGENEOUS CATALYSIS. 1992, 34, 21 284 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153124. GABRIEL WEATHERHEAD
  153125. 7442N
  153126. 2/28/96
  153127. SEPPELT, KONRAD. STRUCTURE, COLOR, AND CHEMISTRY OF PENTAARYL BISMUTH COMPOUNDS. 1992, 34, 207
  153128. 218 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153129. GABRIEL WEATHERHEAD
  153130. 7443N
  153131. 2/28/96V
  153132. TRAVEN, VALERY F.; SHAPAKIN, SERGEI YU. CHARGE
  153133. TRANSFER COMPLEXES OF ORGANOSILICON COMPOUNDS. 1992, 34, 149
  153134. 206 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153135. GABRIEL WEATHERHEAD
  153136. 7444N
  153137. 2/28/96V
  153138. YAMAMOTO, AKIO. CARBON
  153139. OXYGEN BOND ACTIVATION BY TRANSITION METAL COMPLEXES. 1992, 34,111
  153140. 148 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153141. GABRIEL WEATHERHEAD
  153142. 7445N
  153143. 2/28/96V
  153144. KISCH, HORST; HOLZMEIER, PETER. ORGANOMETALLIC CHEMISTRY OF THE N=N GROUP. 1992, 34, 67
  153145. 110 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153146. GABRIEL WEATHERHEAD
  153147. 7446N
  153148. 2/28/96
  153149. BUYERS, PETER K.; CANTY, ALLAN J.; HONEYMAN, THOMAS. ORGANOMETALLIC CHEMISTRY OF PALLADIUM AND PLATINUM WITH POLY(PYRAZOL
  153150. YL)ALKANES AND POLY(PYRAZOL
  153151. YL)BORANES. 1992, 34, 1
  153152. 66 ADVANCES IN ORGANOMETALLIC CHEMISTRY  A REVIEWa
  153153. GABRIEL WEATHERHEAD
  153154. 7447N
  153155. 2/28/96VkSQUIRES, ROBERT R. GAS
  153156. PHASE CARBANION CHEMISTRY. 1992,25(10),461
  153157. 7 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153158. GABRIEL WEATHERHEAD
  153159. 7448N
  153160. 2/28/96V
  153161. RAPPOPORT, ZVI. THE RAPID STEPS IN NUCLEOPHILIC VINYLIC ADDITION
  153162. ELIMINATION SUBSTITUTION. RECENT DEVELOPMENTS. 1992, 25(10), 474
  153163. 9 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153164. GABRIEL WEATHERHEAD
  153165. 7449N
  153166. 2/28/96V
  153167. COLLUM, DAVID B. IS N,N,N',N'
  153168. TETRAMETHYLETHYLENEDIAMINE A GOOD LIGAND FOR LITHIUM? 1992, 25(10), 44854 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153169. GABRIEL WEATHERHEAD
  153170. 7450N
  153171. 2/28/96
  153172. OURISSON, GUY; ROHMER, MICHEL. HOPANOIDS. 2. GEOHOPANOIDS: A NOVEL CLASS OF BACTERIAL LIPIDS. 1992, 25(9),403
  153173. 408 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153174. GABRIEL WEATHERHEAD
  153175. 7451N
  153176. 2/28/96V
  153177. OURISSON, GUY; ALBRECHT, PIERRE. HOPANOIDS. 1. GEOHOPANOIDS: THE MOST ABUNDANT NATURAL PRODUCTS ON EARTH? 1992, 25(9), 398
  153178. 402 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153179. GABRIEL WEATHERHEAD
  153180. 7452N
  153181. 2/28/96V
  153182. OHFUNE, YASUFUMI. STEREOSELECTIVE ROUTES TOWARD THE SYNTHESIS OF UNUSUAL AMINO ACIDS. 1992, 25(8), 360
  153183. 6 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153184. GABRIEL WEATHERHEAD
  153185. 7453N
  153186. 2/28/96V
  153187. OVERMAN, LARRY E. CHARGE AS A KEY COMPONENT IN REACTION DESIGN. THE INVENTION OF CATIONIC CYCLIZATION REACTIONS OF IMPORTANCE IN SYNTHESIS. 1992, 25(8), 352
  153188. 9 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153189. GABRIEL WEATHERHEAD
  153190. 7454N
  153191. 2/28/96
  153192. HARMONY, MARLIN D. THE ELUSIVE EQUILIBRIUM BOND LENGTH IN ORGANIC POLYATOMIC MOLECULES: FINALLY OBTAINABLE FROM SPECTROSCOPY 1992, 25(8), 321
  153193. 7 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153194. GABRIEL WEATHERHEAD
  153195. 7455N
  153196. 2/28/96V
  153197. OSTOVIC, DRAZEN; BRUICE, THOMAS C. MECHANISM OF ALKENE EPOXIDATION BY IRON, CHROMIUM, AND MANGANESE HIGHER VALENT OXO
  153198. METALLOPORPHYRINS. 1992, 25(7), 31430 ACCOUNTS OF CHEMICAL RESEARCH  A REVIEWa
  153199. GABRIEL WEATHERHEAD
  153200. ORG PREP PROCEDURE INT
  153201. CYTOCHROME
  153202. 450 MODEL COMPOUNDS MONO
  153203. OXYGENASE MODEL METALLOPORPHYRIN
  153204. CATALYZED OXYGENATION AQUEOUS SODIUM
  153205. HYPOCHLORITE PHASE
  153206. TRANSFER CATALYSIS OLEFIN EPOXIDATION CALCIUM HYPOCHLORITE MANGANESE(III) PORPHYRIN SELECTIVE OXIDATION 2
  153207. PHASE CONDITIONS SKARZEWSKI J
  153208. 7456N
  153209. 2/28/96V3SYNTHETIC OXIDATIONS WITH HYPOCHLORITES 
  153210.  A REVIEW.W
  153211. 1992 DECX
  153212. 24(6)a
  153213. GABRIEL WEATHERHEAD
  153214. CPHARWOOD INTRAMOLECULAR REVIEW THEORY CALCULATIONS DIELS
  153215. ALDER PRESSURE FURAN MM2M
  153216. 7457N
  153217. 2/28/96V$INTRAMOLECULAR DIELS
  153218. ALDER OF FURANSW
  153219. VOL 114 1992 P 10739a
  153220. GABRIEL WEATHERHEAD
  153221. SYNLETTCcCURRAN SMI2 REVIEW SAMARIUM DIIODIDE BARBIER RADICAL CYCLIZATION SAMARIUM REAGENT MECHANISM WRITINGM
  153222. 7458N
  153223. 2/28/96V[NEW MECHANISTIC INSIGHTS INTO REDUCTION OF HALIDES AND RADICALS WITH SAMARIUM DIIODIDE SMI2W
  153224. 1992 P 943a
  153225. GABRIEL WEATHERHEAD
  153226. TETRAHEDRONClSTANOUNIK DIAZO HETEROAROMATIC REVIEW DIPOLE DIPOLAR CYCLOADDITION AZOMETHINE IMINE HETERO PYRIDAZINE REVIEWM
  153227. 7459N
  153228. 2/28/96Vb1,3
  153229. DIPOLAR CYCLOADDITIONS OF DIAZO ALKANONONES TO SOME NITROGEN CONTAINING HETEROAROMATIC SYSTEMSW
  153230. 1992 P 2925a
  153231. GABRIEL WEATHERHEAD
  153232. ACC CHEM RESCyNICOLAOU ENEDIYNE REVIEW ANTITUMOR CALCHEAMICIN BERGMAN DIRADICAL TRIGGER BIOLOGICAL MM2 RAMBERG BACKLUND ACETYLENE DIENEM
  153233. 7460N
  153234. 2/28/96V3MOLECULAR DESIGN AND BIOLOGICAL ACTION OF ENEDIYNESW
  153235. VOL 25 1992 P 497
  153236. GABRIEL WEATHERHEAD
  153237. SYNLETTC:KASAI MITOMYCIN TARGET AZIRIDINE NIH REVIEW BIOLOGY CANCERM
  153238. 7461N
  153239. 2/28/96V&STUDIES ON THE CHEMISTRY OF MITOMYCINSW
  153240. 1992 P 778a
  153241. GABRIEL WEATHERHEAD
  153242. SYNLETTCQIBUKA REVIEW COPPER CUPRATE ADDITION ENEONE CONJUGATE CHIRAL INDUCTION ASYMMETRICM
  153243. 7462N
  153244. 2/28/96VNNEW ASPECTS OF ORGANOCOPPER REAGENTS.  CHIRAL INDUCTION AND REACTION MECHANISMW
  153245. 1992 P 769a
  153246. GABRIEL WEATHERHEAD
  153247. BOOKC(MOTHERWELL, CRICH; REVIEW, BOOK, RADICALM
  153248. 7463N
  153249. 2/28/96V1FREE
  153250. RADICAL CHAIN REACTIONS IN ORGANIC CHEMISTRYW
  153251. 1991a
  153252. GABRIEL WEATHERHEAD
  153253. B    SYNTHESISC1PETRAGNANI; TELLURIUM, RADICAL, CARBANION, REVIEWM
  153254. 7464N
  153255. 2/28/96V@TELLURIUM REAGENTS IN ORGANIC SYNTHESIS; RECENT ADVANCES, PART 2W
  153256. 1991   897
  153257. GABRIEL WEATHERHEAD
  153258. SYNLETTCSBARRETT; SILANE, CARBANION, PETERSON, OLEFINATION, ALKENE, ALDEHYDE, KETONE, REVIEWM
  153259. 7465N
  153260. 2/28/96
  153261. V3RECENT STUDIES ON THE PETERSON OLEFINATION REACTIONW
  153262. 1991   764
  153263. GABRIEL WEATHERHEAD
  153264. RUSS. CHEM. REV.C4MOISEENKOV; PUMMERER, REARRANGEMENT, SULFIDE, REVIEWM
  153265. 7466N
  153266. 2/28/96V.SYNTHETIC APPLICATION OF THE PUMMERER REACTIONW
  153267. 1991  60  643
  153268. GABRIEL WEATHERHEAD
  153269. PURE APPL. CHEM.CMELIEL; CHELATION, ADDITION, CRAM'S RULE, ALDEHYDE, ALCOHOL, CARBANION, REVIEWM
  153270. 7467N
  153271. 2/28/96V.ASYMMETRIC SYNTHESIS AND CRAM'S (CHELATE) RULEW
  153272. 1991  63  1591
  153273. 1598a
  153274. GABRIEL WEATHERHEAD
  153275. NAT. PROD. REPORTSC<J.P. MICHAEL;  QUINOLIZIDINE, INDOLIZIDINE, ALKALOID, REVIEWM
  153276. 7468N
  153277. 2/28/96V(INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDSW
  153278. 1991  8  553
  153279. GABRIEL WEATHERHEAD
  153280. CHEM. REV.C/MOLANDER; REVIEW, SAMARIUM, LANTHANIDE, RADICALM
  153281. 7469N
  153282. 2/28/96V7APPLICATION OF LANTHANIDE REAGENTS IN ORGANIC SYNTHESISW
  153283. 1992  29
  153284. GABRIEL WEATHERHEAD
  153285. ANGEW, CHEM. INT. ED. ENGL.
  153286. C7M.T. REETZ; AMINO ACID, AMINE, ALDEHYDE, CHIRAL, REVIEWM
  153287. 7470N
  153288. 2/28/96VWNEW APPROACHES TO THE USE OF AMINO ACIDS AS CHIRAL BUILDING BLOCKS IN ORGANIC SYNTHESISW
  153289. 1992  30  1531
  153290. 1546a
  153291. GABRIEL WEATHERHEAD
  153292. ANGEW. CHEM. INT. ED. ENGL.CBH. WALDMANN; LITHIUM PERCHLORATE, SOLVOLYSIS, SUBSTITUTION, REVIEWM
  153293. 7471N
  153294. 2/28/96V1LITHIUM PERCHLORATE IN ETHER 
  153295.  AN UNUSUAL SOLVENTW
  153296. 1992  30  1306
  153297. 1308a
  153298. GABRIEL WEATHERHEAD
  153299. ACCTS. CHEM. RES.C:CHATGILIALOGLU; SILANE, REDUCTION, HALIDE, RADICAL, REVIEWM
  153300. 7472N
  153301. 2/28/96V;ORGANOSILANES AS RADICAL
  153302. BASED REDUCING AGENTS IN SYNTHESISW
  153303. 1992  25  188
  153304. GABRIEL WEATHERHEAD
  153305. ACCTS. CHEM. RES.C9BROWN; REDUCTION, ALCOHOL, CHIRAL, BORANE, REVIEW, PINENEM
  153306. 7473N
  153307. 2/28/96VDASYMMETRIC REDUCTION WITH CHIRAL ORGANOBORANES BASED ON ALPHA PINENEW
  153308. 1992  25  16
  153309. GABRIEL WEATHERHEAD
  153310. TETRAHEDRON
  153311. CWK. BURGESS, I. HENDERSON; CASTANOSPERMINE, INDOLIZIDINE, GLYCOSIDASAE INHIBITOR, REVIEWM
  153312. 7474N
  153313. 2/28/96VFSYNTHETIC APPROACHES TO STEREOISOMERS AND ANALOGUES OF CASTANOSPERMINEW
  153314. 1992  48  4045
  153315. 4066a
  153316. GABRIEL WEATHERHEAD
  153317. TETRAHEDRONCCE. JUARISTI, G. CUEVAS; ANOMERIC EFFECT, ACETAL, ORTHOESTER, REVIEWM
  153318. 7475N
  153319. 2/28/96V%RECENT STUDIES OF THE ANOMERIC EFFECTW
  153320. 1992  48  5019
  153321. 5087a
  153322. GABRIEL WEATHERHEAD
  153323. TETRAHEDRONC
  153324. PADWA; CARBENE, RHODIUM, DIAZO CARBONYL, CYCLOPROPANE, VINYL, REARRANGEMENT, C
  153325. H INSERTION, FURAN, ALKYNE, 1,3
  153326. DIPOLAR CYCLOADDITION, YLIDE FORMATION, SULFONIUM YLIDE, THIOCARBONYL, OXONIUM, CARBONYL YLIDE, AMMONIUM YLIDE, REVIEWM
  153327. 7476N
  153328. 2/28/96VFAPPLICATION OF INTRAMOLECULAR CARBENOID REACTIONS IN ORGANIC SYNTHESISW
  153329. 1992  48  5385
  153330. 5353a
  153331. GABRIEL WEATHERHEAD
  153332. CHEM. REV.C+MOLANDER; SAMARIUM IODIDE, DIIODIDE, REVIEWM
  153333. 7477N
  153334. 2/28/96W
  153335. 1992  92  29a
  153336. GABRIEL WEATHERHEAD
  153337. CHEM. REV.
  153338. CURRAN; RADICAL, REVIEWM
  153339. 7478N
  153340. 2/28/96W
  153341. 1991  91  1237a
  153342. GABRIEL WEATHERHEAD
  153343. CAN. J. CHEM.C)FALLIS; RADICAL, ALPHA HETEROATOM, REVIEWM
  153344. 7479N
  153345. 2/28/96V%ALPHA HETEROATOM SUBSTITUTED RADICALSW
  153346. 1991  69  779a
  153347. GABRIEL WEATHERHEAD
  153348. B    SYNTHESISC
  153349. T.N. MITCHELL; STILLE COUPLING, PALLADIUM, TIN, STANNANE, ALKENE, DIENE, ALKYNE, HALIDE, REVIEW, VINYL TRIFLATE, KETONE, ACID CHLORIDEM
  153350. 7480N
  153351. 2/28/96V4PALLADIUM
  153352. CATALYZED REACTIONS OF ORGANOTIN COMPOUNDSW
  153353. 1992   803
  153354. GABRIEL WEATHERHEAD
  153355. TETRAHEDRONCfPAQUETTE; SUBSTITUTION, ALLYLIC, CYCLOPROPANE, CYCLOBUTANE, N
  153356. YLIDE, SIGMATROPIC REARRANGEMENT, REVIEWM
  153357. 7481N
  153358. 2/28/96V
  153359. THE INTRAMOLECULAR SN' REACTIONW
  153360. 1992  48  7383
  153361. 7423a
  153362. GABRIEL WEATHERHEAD
  153363. TETRAHEDRON ASYMM.CwA.J. WALKER; SULFOXIDE, OXIDATION OF SULFIDES, CARBANION, ADDITION, IMINE, CARBONYL, CONJUGATE ADDITION, REVIEW, CHIRALM
  153364. 7482N
  153365. 2/28/96
  153366. VMASYMMETRIC CARBON
  153367. CARBON BOND FORMATION USING SULFOXIDE
  153368. STABILIZED CARBANIONSW
  153369. 1992  3  961
  153370. GABRIEL WEATHERHEAD
  153371. ADVANCES IN PHOTOCHEMISTRYC.T.J. DOUGHERTY; CANCER, PHOTOCHEMISTRY, REVIEWM
  153372. 7483N
  153373. 2/28/96V)PHOTOCHEMISTRY IN THE TREATMENT OF CANCERW
  153374. 1992  17  275
  153375. GABRIEL WEATHERHEAD
  153376. ORG. REACT.C/MITSUNOBU, REVIEW, ALCOHOL, ESTER, AZIDE, AMIDEM
  153377. 7484N
  153378. 2/28/96V
  153379. THE MITSUNOBU REACTIONW
  153380. 1992  42a
  153381. GABRIEL WEATHERHEAD
  153382. ALDRICHIMICA ACTAC(R.M. WILLIAMS AMINO ACID, CHIRAL, REVIEWM
  153383. 7485N
  153384. 2/28/96V)ASYMMETRIC SYNTHESES OF ALPHA AMINO ACIDSW
  153385. 1992  25  11
  153386. GABRIEL WEATHERHEAD
  153387. TETRAHEDRON ASYMMETRYCJP.J. COX, N.S. SIMPKINS LITHIUM AMIDE BASE, CHIRAL, AMINE, ENOLATE, REVIEWM
  153388. 7486N
  153389. 2/28/96V9ASYMMETRIC SYNTHESIS USING HOMOCHIRAL LITHIUM AMIDE BASESW
  153390. 1991  2  1a
  153391. GABRIEL WEATHERHEAD
  153392. CHEM. REV.C6C.P. JASPERSE, D.P. CURRAN, T.L. FEVIG RADICAL, REVIEWM
  153393. 7487N
  153394. 2/28/96
  153395. 1991  91  1237a
  153396. GABRIEL WEATHERHEAD
  153397. VARIOUSC.VARIOUS  RADICAL, KETYL, CYCLIZATION, SAMARIUMM
  153398. 7488N
  153399. 2/28/96V REVIEWS OF SAMARIUM II CHEMISTRYa
  153400. GABRIEL WEATHERHEAD
  153401. ORG PREP PROCEDURE INTC
  153402. DIELS
  153403. ALDER REACTION PIPECOLIC ACID
  153404. DERIVATIVES FORMAL TOTAL SYNTHESIS PROMOTED BECKMANN REARRANGEMENT L
  153405. GLUTAMIC ACID FIRE ANT VENOM STEREOSELECTIVE SYNTHESIS ASYMMETRIC
  153406. SYNTHESIS CYCLO
  153407. ADDITION REDUCTIVE AMINOCYCLIZATION WANG CLJM
  153408. 7489N
  153409. 2/28/96VURECENT PROGRESS IN THE SYNTHESIS AND REACTIONS OF SUBSTITUTED PIPERIDINES 
  153410.  A REVIEW.W
  153411. 1992 OCTX
  153412. 24(5)a
  153413. GABRIEL WEATHERHEAD
  153414. ORG PREP PROCEDURE INTC
  153415. ASYMMETRIC CLAISEN REARRANGEMENT AXIALLY DISSYMMETRIC MOLECULES ALUMINUM
  153416. HYDRIDE REAGENTS ENANTIOSELECTIVE REDUCTION ACYL SILANES ALPHA,BETA
  153417. UNSATURATED ACYLSILANES NUCLEOPHILIC
  153418. ADDITION ORGANIC
  153419. SYNTHESIS KETONES ALDEHYDES CIRILLO PFM
  153420. 7490N
  153421. 2/28/96V;RECENT PROGRESS IN THE CHEMISTRY OF ACYLSILANES 
  153422.  A REVIEW.W
  153423. 1992 OCTX
  153424. 24(5)a
  153425. GABRIEL WEATHERHEAD
  153426. ORG PREP PROCEDURE INTC1KATRITZKY AR SULTAM REVIEW SULFAMYL FRIEDEL CRAFTM
  153427. 7491N
  153428. 2/28/96V
  153429. PREPARATION OF 6 MEMBERED, 7 MEMBERED AND 8 MEMBERED SULTAMS BY FRIEDEL CRAFTS CYCLIZATION OF OMEGA PHENYLALKANESULFAMOYL CHLORIDES.W
  153430. 1992 AUGX
  153431. 463 467Y
  153432. 24(4)a
  153433. GABRIEL WEATHERHEAD
  153434. ORG PREP PROCEDURE INTC
  153435. X RAY CRYSTAL ASYMMETRICALLY SUBSTITUTED CALIX<4>ARENE IONOPHORIC CALIXARENE ESTERS KINETICALLY STABLE COMPLEXES OPPOSITE PARA POSITIONS LOWER RIM OPTICAL RESOLUTION ALKALI CATIONS RIGIDIFIED CALIX<4>ARENES MOLECULAR STRUCTURE VANLOON JDM
  153436. 7492N
  153437. 2/28/96VWSELECTIVE FUNCTIONALIZATION AND CONFORMATIONAL PROPERTIES OF CALIX<4>ARENES   A REVIEW.W
  153438. 1992 AUGX
  153439. 437 462Y
  153440. 24(4)a
  153441. GABRIEL WEATHERHEAD
  153442. H.M. WALBORSKY , M. TOPOLSKI  CARBANION   GRIGNARD REAGENT  ORGANOMAGNESIUM  RIEKE RECENT REVIEWS (CITED HEREIN) COVER MECHANISM OF GRIGNARD REAGENT FORMATION. HERE, EVIDENCE THAT IT HAPPENS ON SURFACE IS PRESENTED, RATHER THAN AFTER DIFFUSING FROM SURFACE. MAGNESIUM
  153443. 7493N
  153444. 2/28/96V0THE SURFACE NATURE OF GRIGNARD REAGENT FORMATIONW
  153445. 1992  114  3455  3459a
  153446. GABRIEL WEATHERHEAD
  153447. ACCTS CHEM RESCVOVERMAN CATION CYCLIZATION ALKALOID REVIEW WRITING IMINIUM ION COPE CHARGE AZA MANNICHM
  153448. 7494N
  153449. 2/28/96VyCHARGE AS A KEY COMPONENT IN REACTION DESIGN.  THE INVENTION OF CATIONIC CYCLIZATION REACTIONS OF IMPORTANCE IN SYNTHESISW
  153450. VOL 25 1992 P 352a
  153451. GABRIEL WEATHERHEAD
  153452. 7495N
  153453. 2/28/96V
  153454. YALKOWSKY, SAMUEL H.; BANERJEE, SUJIT. AQUEOUS SOLUBILITY: METHODS FOR ESTIMATION OF ORGANIC COMPOUNDS. DEKKER: NEW YORK, 1992. A REVIEWa
  153455. GABRIEL WEATHERHEAD
  153456. 7496N
  153457. 2/28/96
  153458. VORONKOV, M. G.; MALETINA, E. A.; ROMAN, V. K. HETEROSILOXANES, VOL. II: DERIVATIVES OF NITROGEN AND PHOSPHORUS (TRANSLATED BY PAUL CURTIS). HARWOOD ACADEMIC PUBL.: CHUR, SWITZERLAND, 1991. A REVIEWa
  153459. GABRIEL WEATHERHEAD
  153460. 7497N
  153461. 2/28/96VlTUNDO, PIETRO. CONTINUOUS FLOW METHODS IN ORGANIC SYNTHESIS. ELLIS HORWOOD: CHICHESTER, U.K., 1991. A REVIEWa
  153462. GABRIEL WEATHERHEAD
  153463. 7498N
  153464. 2/28/96VzTHOMAS, SUSAN E.; ED. ORGANIC SYNTHESIS: THE ROLES OF BORON AND SILICON. OXFORD UNIVERSITY PRESS: NEW YORK, 1991. A REVIEWa
  153465. GABRIEL WEATHERHEAD
  153466. 7499N
  153467. 2/28/96VuTERRIER, FRANCOIS. NUCLEOPHILIC AROMATIC DISPLACEMENT THE INFLUENCE OF THE NITRO GROUP. VCH: NEW YORK, 1991. A REVIEWa
  153468. GABRIEL WEATHERHEAD
  153469. 7500N
  153470. 2/28/96VbSMITH, MICHAEL B. COMPENDIUM OF ORGANIC SYNTHETIC METHODS, VOL. 7. WILEY: NEW YORK, 1992. A REVIEWa
  153471. GABRIEL WEATHERHEAD
  153472. 7501N
  153473. 2/28/96
  153474. SHAIK, SASON S.; SCHLEGEL, H. BERNHARD; WOLFE, SAUL. THEORETICAL ASPECTS OF PHYSICAL ORGANIC CHEMISTRY. THE SN2 MECHANISMS. WILEY: NEW YORK, 1992. A REVIEWa
  153475. GABRIEL WEATHERHEAD
  153476. 7502N
  153477. 2/28/96V{RAHMAN, ATTA
  153478. UR; AHMAD, VIQAR UDDIN, EDS. 13C
  153479. NMR OF NATURAL PRODUCTS. VOL. 2. DITERPENES. PLENUM: NEW YORK, 1992. A REVIEWa
  153480. GABRIEL WEATHERHEAD
  153481. 7503N
  153482. 2/28/96V
  153483. PATAI, SAUL; RAPPOPORT, ZVI, EDS. THE CHEMISTRY OF AMIDINES AND IMIDATES, VOL. 2. (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1991. A REVIEWa
  153484. GABRIEL WEATHERHEAD
  153485. 7504N
  153486. 2/28/96VnPATAI, SAUL. PATAI'S 1992 GUIDE TO THE CHEMISTRY OF FUNCTIONAL GROUPS. WILEY: CHICHESTER, U.K., 1992. A REVIEWa
  153487. GABRIEL WEATHERHEAD
  153488. 7505N
  153489. 2/28/96V
  153490. PASTO, DANIEL, J.; JOHNSON, CARL, R.; MILLER, MARVIN J. EXPERIMENTS AND TECHNIQUES IN ORGANIC CHEMISTRY. PRENTICE HALL: ENGLEWOOD CLIFFS, NJ, 1992. A REVIEWa
  153491. GABRIEL WEATHERHEAD
  153492. 7506N
  153493. 2/28/96VSO'HAGAN, DAVID. THE POLYKETIDE METABOLITES. ELLIS HORWOOD: NEW YORK, 1991. A REVIEWa
  153494. GABRIEL WEATHERHEAD
  153495. 7507N
  153496. 2/28/96V
  153497. NIESSEN, W. M. A.; VAN DER GREEF, J. LIQUID CHROMATOGRAPHY
  153498. MASS SPECTROMETRY. PRINCIPLES AND APPLICATIONS (CHROMATOGRAPHIC SCIENCE SERIES, VOL. 58). DEKKER: NEW YORK, 1992. A REVIEWa
  153499. GABRIEL WEATHERHEAD
  153500. 7508N
  153501. 2/28/96V
  153502. LUND, HENNING; BAIZER, MANUEL M.; EDS. ORGANIC ELECTROCHEMISTRY. AN INTRODUCTION AND A GUIDE, 3RD. ED., REVISED AND EXPANDED. DEKKER: NEW YORK, 1991. A REVIEWa
  153503. GABRIEL WEATHERHEAD
  153504. 7509N
  153505. 2/28/96VxLUKEVICS, EDMUNDS.; ZABLOCKA, ALLA. NUCLEOSIDE SYNTHESIS, ORGANOSILICON METHODS. ELLIS HORWOOD: NEW YORK, 1991. A REVIEWa
  153506. GABRIEL WEATHERHEAD
  153507. 7510N
  153508. 2/28/96VrLINDBERG, THOMAS, ED. STRATEGIES AND TACTICS IN ORGANIC SYNTHESIS, VOL. 3. ACADEMIC: SAN DIEGO, CA, 1991. A REVIEWa
  153509. GABRIEL WEATHERHEAD
  153510. 7511N
  153511. 2/28/96
  153512. KARCHER, W.; DEVILLERS, J.; GARRIGUES, PH.; JACOB, T., EDS. SPECTRAL ATLAS OF POLYCYCLIC AROMATIC COMPOUNDS, VOL. 3. KLUWER ACADEMIC PUBLISHERS: DORDRECHT, THE NETHERLANDS, 1991. A REVIEWa
  153513. GABRIEL WEATHERHEAD
  153514. 7512N
  153515. 2/28/96VqHO, TSE
  153516. LOK. ENANTIOSELECTIVE SYNTHESIS OF NATURAL PRODUCTS FROM CHIRAL TERPENES. WILEY: NEW YORK, 1992. A REVIEWa
  153517. GABRIEL WEATHERHEAD
  153518. 7513N
  153519. 2/28/96V
  153520. HEFTMANN, ERICH, ED. CHROMATOGRAPHY, 5TH ED. FUNDAMENTALS AND APPLICATIONS OF CHROMATOGRAPHY AND RELATED DIFFERENTIAL MIGRATION METHODS, PT B: APPLICATIONS (JOURNAL OF CHROMATOGRAPHY LIBRARY, VOL. 51B). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1992. A REVIEWa
  153521. GABRIEL WEATHERHEAD
  153522. 7514N
  153523. 2/28/96V
  153524. HILL, R. A.; ET AL., EDS. DICTIONARY OF STEROIDS: CHEMICAL DATA, STRUCTURES AND BIBLIOGRAPHIES, VOLS. 1 AND 2. CHAPMAN AND HALL: LONDON, 1991. A REVIEWa
  153525. GABRIEL WEATHERHEAD
  153526. 7515N
  153527. 2/28/96
  153528. V|HALEVI, E. AMITAI. ORBITAL SYMMETRY AND REACTION MECHANISM. THE OCAMS VIEW. SPRINGER
  153529. VERLAG: BERLIN, GERMANY, 1992. A REVIEWa
  153530. GABRIEL WEATHERHEAD
  153531. 7516N
  153532. 2/28/96VjFIESER, MARY. FIESER AND FIESER'S REAGENTS FOR ORGANIC SYNTHESIS, VOL. 16. WILEY: NEW YORK, 1992. A REVIEWa
  153533. GABRIEL WEATHERHEAD
  153534. 7517N
  153535. 2/28/96V
  153536. ATWOOD, J. L.; DAVIES, J. E. D.; MACNICOL, D. D.; EDS. INCLUSION COMPOUNDS, VOL. 4: KEY ORGANIC HOST SYSTEMS. OXFORD UNIV. PRESS: OXFORD, U.K., 1991. A REVIEWa
  153537. GABRIEL WEATHERHEAD
  153538. 7518N
  153539. 2/28/96V
  153540. ALBIZATI, K. F.; MARTIN, V. A.; AGHARAHIMI, M. R.; STOLZE D. A.; EDS. BIOORGANIC MARINE CHEMISTRY, VOL 6: SYNTHESIS OF MARINE NATURAL PRODUCTS 2. NONTERPENOIDS. SPRINGER: BERLIN, GERMANY, 1992. A REVIEWa
  153541. GABRIEL WEATHERHEAD
  153542. 7519N
  153543. 2/28/96
  153544. ALBIZATI, K. F.; MARTIN, V. A.; AGHARAHIMI, M. R.; STOLZE, D. A.; EDS. BIOORGANIC MARINE CHEMISTRY, VOL. 5: SYNTHESIS OF MARINE NATURAL PRODUCTS 1. TERPENOIDS. SPRINGER: BERLIN, GERMANY, 1992. A REVIEWa
  153545. GABRIEL WEATHERHEAD
  153546. 7520N
  153547. 2/28/96VeAPSIMON, JOHN; ED. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOLUME 9. WILEY: NEW YORK, 1992. A REVIEWa
  153548. GABRIEL WEATHERHEAD
  153549. 7521N
  153550. 2/28/96V
  153551. TODA, FUMIO. MOLECULAR RECOGNITION IN THE SOLID STATE. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 2, GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153552. GABRIEL WEATHERHEAD
  153553. 7522N
  153554. 2/28/96V
  153555. MITOV, M. D.; FAUCON, J. F.; MELEARD, P.; BOROTHEL, P. THERMAL FLUCTUATIONS OF MEMBRANES. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 2, GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153556. GABRIEL WEATHERHEAD
  153557. 7523N
  153558. 2/28/96
  153559. AOYAMA, YASUHIRO. ACCUMULATION OF UNIT
  153560. BINDING SITES: HYDROGEN BONDING FIXATION IN MULTI
  153561. FUNCTIONAL POLAR ORGANIC MOLECULES. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 2, GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153562. GABRIEL WEATHERHEAD
  153563. 7524N
  153564. 2/28/96V
  153565. FUBRHOP, JURGEN
  153566. HEINRICH; BACH, REINHARD. MONOLAYER LIPID MEMBRANES (MLMS) FROM BIOAMPHIPHILES. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 2, GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153567. GABRIEL WEATHERHEAD
  153568. 7525N
  153569. 2/28/96V
  153570. KAIFER, ANGEL. CYCLODEXTRIN COMPLEXATION OF AMPHIPHILIC COMPOUNDS. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 2, GEORGE W. GOKEL, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153571. GABRIEL WEATHERHEAD
  153572. 7526N
  153573. 2/28/96
  153574. KRANTZ, ALAN. SOME THOUGHTS ON ENZYME INHIBITORS AND THE QUIESCENT AFFINITY LABEL CONCEPT. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153575. GABRIEL WEATHERHEAD
  153576. 7527N
  153577. 2/28/96V
  153578. ALBRECHT, HARRY A.; CHRISTENSON, JAMES G. MECHANISM
  153579. BASED
  153580. ACTION CEPHALOSPORINS. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153581. GABRIEL WEATHERHEAD
  153582. 7528N
  153583. 2/28/96V
  153584. KOZIKOVVSKI, ALAN P.; THIELS, EDDA; TANG, X. C.; HANIN, ISRAEL. HUPERAZINE A
  153585. A POSSIBLE LEAD STRUCTURE IN THE TREATMENT OF ALZHEIMER'S DISEASE. A REVIEWa
  153586. GABRIEL WEATHERHEAD
  153587. 7529N
  153588. 2/28/96V
  153589. LIVINGSTON, DOUGLAS A. APPLICATION OF SILICON CHEMISTRY IN THE CORTICOSTEROID FIELD. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEW
  153590. GABRIEL WEATHERHEAD
  153591. 7530N
  153592. 2/28/96V
  153593. MUCHOWSKI, JOSEPH M. THE DEVELOPMENT OF KETOROLAC: IMPACT ON PYRROLE CHEMISTRY AND ON PAIN THERAPY. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153594. GABRIEL WEATHERHEAD
  153595. 7531N
  153596. 2/28/96V
  153597. SHINKAI, ICHIRO; SIGAL, NOLAN H. CHEMISTRY AND BIOLOGY OF THE IMMUNOSUPPRESSANT (
  153598. 504. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153599. GABRIEL WEATHERHEAD
  153600. 7532N
  153601. 2/28/96V
  153602. WENDER, PAUL A.; CRIBBS, CYNTHIA M. COMPUTER ASSISTED MOLECULAR DESIGN RELATED TO THE PROTEIN KINASE C RECEPTOR. ADVANCES IN MEDICINAL CHEMISTRY. VOLUME 1, BRUCE E. MARYANOFF, CYNTHIA A. MARYANOFF, EDS., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153603. GABRIEL WEATHERHEAD
  153604. 7533N
  153605. 2/28/96
  153606. MOODY, CHRISTOPHER J.; REES, CHARLES W.; THOMAS, ROBERT. THE PYRIDOACRIDINE ALKALOIDS. ADVANCES IN HETEROCYCLIC NATURAL PRODUCT SYNTHESIS VOLUME 2, WILLIAM H. PEARSON, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153607. GABRIEL WEATHERHEAD
  153608. 7534N
  153609. 2/28/96
  153610. %HARRING, SCOTT R.; EDSTROM, ERIC D.; LIVINGHOUSE, TOM. EPISULFONIUM IONS AND EPISELENONIUM IONS. VERSATILE HETEROCYCLIC CATIONS FOR THE SYNTHESIS OF NATURAL PRODUCTS. ADVANCES IN HETEROCYCLIC NATURAL PRODUCT SYNTHESIS VOLUME 2, WILLIAM H. PEARSON, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEW
  153611. GABRIEL WEATHERHEAD
  153612. 7535N
  153613. 2/28/96V
  153614. JACOBI, PETER A. BIS
  153615. HETERIANNULATION: TOTAL SYNTHESIS OF FURANOTERPENES, BUTENOLIDES, LACTONES AND RELATED MATERIALS. ADVANCES IN HETEROCYCLIC NATURAL PRODUCT SYNTHESIS VOLUME 2, WILLIAM H. PEARSON, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153616. GABRIEL WEATHERHEAD
  153617. 7536N
  153618. 2/28/96
  153619. FUKUYAMA, TOHRU. SYNTHESIS OF NAPHTHYRIDINOMYCIN. ADVANCES IN HETEROCYCLIC NATURAL PRODUCT SYNTHESIS VOLUME 2, WILLIAM H. PEARSON, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEWa
  153620. GABRIEL WEATHERHEAD
  153621. 7537N
  153622. 2/28/96
  153623. (BOGER, DALE L. DESIGN, SYNTHESIS AND EVALUATION OF FUNCTIONAL ANALOGS OF CC
  153624. 1065 AND THE OUARCARMYCINS: A STUDY OF STRUCTURAL FEATURES EFFECTING DNA BINDING SELECTIVITY. ADVANCES IN HETEROCYCLIC NATURAL PRODUCT SYNTHESIS VOLUME 2, WILLIAM H. PEARSON, ED., JAI PRESS: GREENWICH, CT, 1992. A REVIEW
  153625. GABRIEL WEATHERHEAD
  153626. 7538N
  153627. 2/28/96V
  153628. MARSON, CHARLES M. REACTIONS OF CARBONYL COMPOUNDS WITH (MONOHALO) METHYLENIMINIUM SALTS (VILSMEIER REAGENTS). TETRAHEDRON 1992, 48(18), 3659
  153629. 726. A REVIEWa
  153630. GABRIEL WEATHERHEAD
  153631. 7539N
  153632. 2/28/96
  153633. CHEN, JIANXIN; SCHEFFER, JOHN R.; TROTTER, JAMES. DIFFERENCES IN PHOTOCHEMICAL REACTIVITY OF 9,10
  153634. ETHENOANTHRACENE DERIVATIVES IN LIQUID AND CRYSTALLINE MEDIA TETRAHEDRON 1992, 48(16), 3251
  153635. 74. A REVIEWa
  153636. GABRIEL WEATHERHEAD
  153637. 7540N
  153638. 2/28/96V
  153639. AGER DAVID J.; EAST, MICHAEL B. METHODOLOGY TO ESTABLISH 1,2
  153640.  AND 1,3
  153641. DIFUNCTIONALITY FOR THE SYNTHESIS OF CARBOHYDRATE DERIVATIVES. TETRAHEDRON 1992, 48(14), 2803
  153642. 94. A REVIEWa
  153643. GABRIEL WEATHERHEAD
  153644. 7541N
  153645. 2/28/96VxSCOTT, A. IAN. GENETICALLY ENGINEERED SYNTHESIS OF COMPLEX NATURAL PRODUCTS. TETRAHEDRON 1992, 48(13), 2559
  153646. 78. A REVIEWa
  153647. GABRIEL WEATHERHEAD
  153648. 7542N
  153649. 2/28/96V
  153650. SCHREIBER, STUART L.; LIU, JUN
  153651.  ALBERS, MARK W.; ROSEN MICHAEL K.; STANDAERT, ROBERT F.; WANDLESS, THOMAS J.; SOMERS, PATRICIA K. MOLECULAR RECOGNITION OF IMMUNOPHILINS AND IMMUNOPHILIN
  153652. LIGAND COMPLEXES. TETRAHEDRON 1992, 48(13), 2545
  153653. 58. A REVIEWa
  153654. GABRIEL WEATHERHEAD
  153655. 7543N
  153656. 2/28/96
  153657. VvBARTON, D. H. R. THE INVENTION OF CHEMICAL REACTIONS: THE LAST FIVE YEARS. TETRAHEDRON 1992, 48(13), 2529
  153658. 44. A REVIEWa
  153659. GABRIEL WEATHERHEAD
  153660. 7544N
  153661. 2/28/96V
  153662. FERREIRA, DANEEL; STEYNBERG, JAN P.; ROUX, DAVID G.; BRANDT, E. VINCENT. DIVERSITY OF STRUCTURE AND FUNCTION IN OLIGOMERIC FLAVANOIDS. TETRAHEDRON 1992, 48(10),1743
  153663. 803. A REVIEWa
  153664. GABRIEL WEATHERHEAD
  153665. 7545N
  153666. 2/28/96V
  153667. KALININ, V. N. CARBON
  153668. CARBON BOND FORMATION IN HETEROCYCLES USING NICKEL AND PALLADIUM CATALYZED REACTIONS. SYNTHESIS 1992, (5), 413
  153669. 32. A REVIEWa
  153670. GABRIEL WEATHERHEAD
  153671. 7546N
  153672. 2/28/96VnMINAMI, TORU; MOTOYOSHIYA, JIRO. VINYLPHOSPHONATES IN ORGANIC SYNTHESIS. SYNTHESIS 1992, (4), 333
  153673. 49. A REVIEWa
  153674. GABRIEL WEATHERHEAD
  153675. 7547N
  153676. 2/28/96V
  153677. CINTAS, PEDRO. ADDITION OF ORGANOCHROMIUM COMPOUNDS TO ALDEHYDES: THE NOZAKI
  153678. HIYAMA REACTION. SYNTHESIS 1992, (3), 248
  153679. 57. A REVIEWa
  153680. GABRIEL WEATHERHEAD
  153681. 7548N
  153682. 2/28/96
  153683. DEMIR, AYHAN S., JEGANATHAN, ALWARSAMY. SELECTIVE OXIDATION OF ALPHA,BETA
  153684. UNSATURATED KETONES AT THE ALPHA'
  153685. POSITION. SYNTHESIS 1992, (3), 235
  153686. 47. A REVIEWa
  153687. GABRIEL WEATHERHEAD
  153688. 7549N
  153689. 2/28/96V
  153690. DUEHOLM, KIM L.; PEDERSEN, ERIK B. 2,3
  153691. DIDEOXYFURANOSES IN CONVERGENT SYNTHESES OF 2',3'
  153692. DIDEOXY NUCLEOSIDES. SYNTHESIS 1992, (1
  153693. 22. A REVIEWa
  153694. GABRIEL WEATHERHEAD
  153695. 7550N
  153696. 2/28/96V
  153697. MIKAMI, KOICHI; TERADA, MASAHIRO; NARISAWA, SATOSHI; NAKAI, TAKESHI. ASYMMETRIC CATALYSIS FOR CARBONYL
  153698. ENE REACTION. SYNLETT 1992, (4), 255
  153699. 65. A REVIEWa
  153700. GABRIEL WEATHERHEAD
  153701. 7551N
  153702. 2/28/96V
  153703. BERGSTROM, DON; LIN, XIAOPING, WANG, GUANGYI; ROTSTEIN, DAVID; BEAL, PETER; NORRIX, KATHRYN; RUTH, JERRY. C
  153704. 5 SUBSTITUTED NUCLEOSIDE ANALOGS. SYNLETT 1992, (3),179
  153705. 88. A REVIEWa
  153706. GABRIEL WEATHERHEAD
  153707. 7552N
  153708. 2/28/96
  153709. INOGUCHI, KIYOSHI; SAKURABA, SHUNJI; ACHIWA, KAZUO. DESIGN CONCEPTS FOR DEVELOPING HIGHLY EFFICIENT CHIRAL BISPHOSPHINE LIGANDS IN RHODIUM
  153710. CATALYZED ASYMMETRIC HYDROGENATIONS. SYNLETT 1992, (3),169
  153711. 78. A REVIEWa
  153712. GABRIEL WEATHERHEAD
  153713. 7553N
  153714. 2/28/96V
  153715. DAHL, OTTO. PREPARATION OF NUCLEOSIDE PHOSPHOROTHIOATES PHOSPHORODITHIOATES AND RELATED COMPOUNDS. SULFUR REPORTS 1991,11(1) 167
  153716. 92. A REVIEWa
  153717. GABRIEL WEATHERHEAD
  153718. 7554N
  153719. 2/28/96V
  153720. BABU, B. RAMESH; RAMANA, D. V.; RAMADAS, S. R. SYNTHESIS OF CONDENSED THIAZOLO[3,2
  153721. ALPHA]PYRIMIDINE SYSTEMS. SULFUR REPORTS 1991, 11(1), 143
  153722. 65. A REVIEWa
  153723. GABRIEL WEATHERHEAD
  153724. 7555N
  153725. 2/28/96VsRUDORF, WOLF DIETER. REACTIONS OF CARBON DISULFIDE WITH C
  153726. NUCLEOPHILES. SULFUR REPORTS 1991,11(1), 51
  153727. 141. A REVIEWa
  153728. GABRIEL WEATHERHEAD
  153729. 7556N
  153730. 2/28/96
  153731. GUSAROVA, N. K.; TATARINOVA, A. A.; SINEGOVSKAYA, L. M. VINYL TELLURIDES: SYNTHESIS AND PROPERTIES. SULFUR REPORTS 1991,11(1),1
  153732. 50. A REVIEWa
  153733. GABRIEL WEATHERHEAD
  153734. 7557N
  153735. 2/28/96V
  153736. TROST, BARRY M. THE ATOM ECONOMY: A SEARCH FOR SYNTHETIC EFFICIENCY. SCIENCE (WASHINGTON, D.C. 1883
  153737. ) 1991, 254(5037),1471
  153738. 7. A REVIEWa
  153739. GABRIEL WEATHERHEAD
  153740. 7558N
  153741. 2/28/96V
  153742. WHITESIDES, GEORGE M.
  153743.  MATHIAS, JOHN P., SETO, CHRISTOPHER T. MOLECULAR SELF
  153744. ASSEMBLY AND NANOCHEMISTRY: A CHEMICAL STRATEGY FOR THE SYNTHESIS OF NANOSTRUCTURES. SCIENCE (WASHINGTON, D.C. 1883
  153745. ) 1991, 254(5036), 1312
  153746. 19. A REVIEWa
  153747. GABRIEL WEATHERHEAD
  153748. 7559N
  153749. 2/28/96V
  153750. SISKIN, MICHAEL; KATRITZKY, ALAN R. REACTIVITY OF ORGANIC COMPOUNDS IN HOT WATER: GEOCHEMICAL AND TECHNOLOGICAL IMPLICATIONS. SCIENCE (WASHINGTON, D.C. 1883
  153751. ) 1991, 254(5029), 231
  153752. 7. A REVIEWa
  153753. GABRIEL WEATHERHEAD
  153754. 7560N
  153755. 2/28/96
  153756. HUGHES, R. C.; RICCO, A. J.; BUTLER, M. A.; MARTIN, S. J. CHEMICAL MICROSENSORS. SCIENCE (WASHINGTON, D.C. 1883
  153757. ) 1991, 254(5028), 74
  153758. 80. A REVIEWa
  153759. GABRIEL WEATHERHEAD
  153760. 7561N
  153761. 2/28/96V
  153762. CHIANG, YVONNE; KRESGE, A. JERRY. ENOLS AND OTHER REACTIVE SPECIES. SCIENCE (WASHINGTON, D.C. 1883
  153763. ) 1991, 253(5018), 395
  153764. 400. A REVIEWa
  153765. GABRIEL WEATHERHEAD
  153766. 7562N
  153767. 2/28/96V
  153768. VERKHOVSKAYA, M. A.; YAMSKOV, I. A. ENZYMIC METHODS OF RESOLVING RACEMATES OF AMINO ACIDS AND THEIR DERIVATIVES. RUSSIAN CHEMICAL REVIEWS 1991, 60(10), 1163
  153769. 79. A REVIEWa
  153770. GABRIEL WEATHERHEAD
  153771. 7563N
  153772. 2/28/96V
  153773. ZABIROV, N. G.; SHAMSEVALEEV, F. M.; CHERKASOV, R. A. N
  153774. PHOSPHORYLATED AMIDES AND THIOAMIDES. RUSSIAN CHEMICAL REVIEWS 1991, 60(10), 1128
  153775. 44. A REVIEWa
  153776. GABRIEL WEATHERHEAD
  153777. 7564N
  153778. 2/28/96V
  153779. MASTRYUKOVA, T. A.; KABACHNIK, M. I. ENOLIZATION OF THE PHOSPHORYL GROUP. RUSSIAN CHEMICAL REVIEWS 1991, 60(10),1115
  153780. 27. A REVIEWa
  153781. GABRIEL WEATHERHEAD
  153782. 7565N
  153783. 2/28/96V
  153784. TAKHISTOV, V. V.; RODIN, A. A.; MAKSIMOVA, B. N. MASS SPECTROMETRY OF HALOGEN
  153785. CONTAINING ORGANIC COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(10), 1101
  153786. 1114. A REVIEWa
  153787. GABRIEL WEATHERHEAD
  153788. 7566N
  153789. 2/28/96V
  153790. MAIRANOVSKII, S. G. THE ELECTROREDUCTION OF ORGANIC COMPOUNDS IN THE PRESENCE OF CATALYSTS CAUSING CATALYTIC EVOLUTION OF HYDROGEN AND THE ELECTROSYNTHESIS OF CHIRAL COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(10), 1085
  153791. 1100. A REVIEWa
  153792. GABRIEL WEATHERHEAD
  153793. 7567N
  153794. 2/28/96V
  153795. DVORKO, G. F.; PONOMAREVA, E. A. THE VERDAZYL METHOD FOR THE STUDY OF THE KINETICS AND MECHANISMS OF THE UNIMOLECULAR HETEROLYSIS REACTIONS OF ORGANIC COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1991 60(10), 1071
  153796. 84. A REVIEWa
  153797. GABRIEL WEATHERHEAD
  153798. 7568N
  153799. 2/28/96
  153800. KUKHAR, V. P.; YAGUPOL'SKII, YU L.; GERUS, I. I.; KOLYCHEVA, M. T. FLUORINE
  153801. CONTAINING AROMATIC AMINO ACIDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(9), 1050
  153802. 58. A REVIEWa
  153803. GABRIEL WEATHERHEAD
  153804. 7569N
  153805. 2/28/96VoSHAPIRO, YU. M. GEM
  153806. POLYOLS
  153807. A UNIQUE CLASS OF COMPOUND. RUSSIAN CHEMICAL REVIEWS 1991, 60(9), 1035
  153808. 49. A REVIEWa
  153809. GABRIEL WEATHERHEAD
  153810. 7570N
  153811. 2/28/96V
  153812. ANDRUSHKEVICH, T. V.; POPOVA, G. YA. MECHANISM OF THE HETEROGENEOUS OXIDATION OF ACROLEIN TO ACRYLIC ACID. RUSSIAN CHEMICAL REVIEWS 1991, 60(9), 1023
  153813. 1234. A REVIEWa
  153814. GABRIEL WEATHERHEAD
  153815. 7571N
  153816. 2/28/96VoKLABUNOVSKII, E. I. ASYMMETRIC HYDROGENATION ON METALS. RUSSIAN CHEMICAL REVIEWS 1991, 60(9), 980
  153817. 995. A REVIEWa
  153818. GABRIEL WEATHERHEAD
  153819. 7572N
  153820. 2/28/96V
  153821. RYAKHOVSKII, V. V.; AGAFONOV, S. V.; KOSYREV, YU. M. SPECIAL FEATURES OF THE SYNTHESIS OF PEPTIDES CONTAINING SECONDARY AMINO ACIDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(8), 924
  153822. 33. A REVIEW
  153823. GABRIEL WEATHERHEAD
  153824. 7573N
  153825. 2/28/96V
  153826. ISHCHENKO, A. A. STRUCTURE AND SPECTRAL
  153827. LUMINESCENT PROPERTIES OF POLYMETHINE DYES. RUSSIAN CHEMICAL REVIEWS 1991, 60(8), 865
  153828. 84. A REVIEWa
  153829. GABRIEL WEATHERHEAD
  153830. 7574N
  153831. 2/28/96V
  153832. KUKHAR', V. P.; SOLOSHONOK, V. A. ALIPHATIC FLUORINE
  153833. CONTAINING AMINO ACIDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(8), 850
  153834. 64. A REVIEWa
  153835. GABRIEL WEATHERHEAD
  153836. 7575N
  153837. 2/28/96V
  153838. KOVAL', I. V. PROGRESS IN THE CHEMISTRY OF PERHALOMETHANESULPHENYL HALIDES. RUSSIAN CHEMICAL REVIEWS RUSSIAN CHEMICAL REVIEWS 1991, 60(8), 830
  153839. 49. A REVIEWa
  153840. GABRIEL WEATHERHEAD
  153841. 7576N
  153842. 2/28/96V
  153843. GALKIN, V. I.; SAYAKHOV, R. D.; CHAERKASOV, R. A. STERIC EFFECTS: THE PROBLEM OF THEIR QUANTITATIVE ASSESSMENT AND MANIFESTATION IN THE REACTIVITY OF HETERO
  153844. ORGANIC COMPOUNDS. RUSSIAN CHEMICAL REVIEWS 1991, 60(8), 815
  153845. 29. A REVIEWa
  153846. GABRIEL WEATHERHEAD
  153847. 7577N
  153848. 2/28/96
  153849. STONE, J. A. HIGH PRESSURE MASS SPECTROMETRIC STUDIES OF SILICON
  153850. CONTAINING IONS. RESEARCH ON CHEMICAL INTERMEDIATES 199L, 16(3), 257
  153851. 78. A REVIEWa
  153852. GABRIEL WEATHERHEAD
  153853. 7578N
  153854. 2/28/96V
  153855. XIE, R. Q.; LIU, Y. C.; LEI, X. G. FLUOROSPECTROCHEMISTRY WITHIN CYCLODEXTRIN CAVITIES. RESEARCH ON CHEMICAL INTERMEDIATES 1991,16(1), 71
  153856. 95. A REVIEWa
  153857. GABRIEL WEATHERHEAD
  153858. 7579N
  153859. 2/28/96V
  153860. KEVAN, L.; YU, J. S. COPPER ION CATALYSIS OF COMPLETE AND PARTIAL OXIDATION OF PROPYLENE ON X AND Y ZEOLITES: CORRELATION OF ELECTRON SPIN RESONANCE AND PRODUCT ANALYSIS. RESEARCH ON CHEMICAL INTERMEDIATES 1991, 15(1), 67
  153861. 80. A REVIEWa
  153862. GABRIEL WEATHERHEAD
  153863. 7580N
  153864. 2/28/96V
  153865. RICCI, A.; REGINATO, G.; DEGL'INNOCENTI, A.; SECONI, G. ORGANOMETALLIC POLYSYNTHONS: A NOVEL STRATEGY FOR SELECTIVELY POLYFUNCTIONALIZED MOLECULES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 439
  153866. 46. A REVIEWa
  153867. GABRIEL WEATHERHEAD
  153868. 7581N
  153869. 2/28/96
  153870. BACKVALL, JAN
  153871. E. PALLADIUM
  153872. CATALYZED INTRAMOLECULAR 1,4
  153873. ADDITIONS TO CONJUGATED DIENES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 429
  153874. 37. A REVIEWa
  153875. GABRIEL WEATHERHEAD
  153876. 7582N
  153877. 2/28/96V
  153878. HAYASHI, TAMIO; KUBO, AKIHITO; OZAWA, FUMIYUKI. CATALYTIC ASYMMETRIC ARYLATION OF OLEFINS. PURE AND APPLIED CHEMISTRY 1992, 64(3), 421
  153879. 27. A REVIEWa
  153880. GABRIEL WEATHERHEAD
  153881. 7583N
  153882. 2/28/96VxKELLOGG, RICHARD M. ENZYME MODELS AND ORGANOMETALLIC CHEMISTRY. PURE AND APPLIED CHEMISTRY 1992, 64(3), 413
  153883. 20. A REVIEWa
  153884. GABRIEL WEATHERHEAD
  153885. 7584N
  153886. 2/28/96V
  153887. MURAHASHI, SHUNICHI. BIOMIMETIC OXIDATION IN ORGANIC SYNTHESIS USING TRANSITION METAL CATALYSTS. PURE AND APPLIED CHEMISTRY 1992, 64(3), 403
  153888. 12. A REVIEWa
  153889. GABRIEL WEATHERHEAD
  153890. 7585N
  153891. 2/28/96V|ERKER, GERHARD. STEREOSELECTIVE SYNTHESIS WITH ZIRCONIUM COMPLEXES. PURE AND APPLIED CHEMISTRY 1992, 64(3),393
  153892. 401. A REVIEWa
  153893. GABRIEL WEATHERHEAD
  153894. 7586N
  153895. 2/28/96
  153896. ALEXAKIS, ALEX. STEREOCHEMICAL ASPECTS OF THE FORMATION OF CHIRAL ALLENES FROM PROPARGYLIC ETHERS AND EPOXIDES PURE AND APPLIED CHEMISTRY 1992, 64(3),387
  153897. 92. A REVIEWa
  153898. GABRIEL WEATHERHEAD
  153899. 7587N
  153900. 2/28/96V
  153901. DAVIES, STEPHEN G.; DONOHOE, TIMOTHY J.; WILLIAMS, JONATHAN M. J. STEREOSELECTIVE MANIPULATION OF ACETALS DERIVED FROM O
  153902. SUBSTITUTED BENZALDEHYDE CHROMIUM TRICARBONYL COMPLEXES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 379
  153903. 86. A REVIEWa
  153904. GABRIEL WEATHERHEAD
  153905. 7588N
  153906. 2/28/96V
  153907. HILL, LAWRENCE; RICHARDS, CHRISTOPHER J.; SABERI, STEPHEN P.; THOMAS, SUSAN E. SYNTHESIS AND REACTIVITY OF IRON TRICARBONYL COMPLEXES OF VINYLKETENES, VINYLKETENIMINES AND VINYLALLENES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 371
  153908. 7. A REVIEWa
  153909. GABRIEL WEATHERHEAD
  153910. 7589N
  153911. 2/28/96
  153912. KNOCHEL, PAUL; ROZEMA, MICHAEL J.; TUCKER, CHARLES E.; RETHERFORD, CAROLE; FURLONG, MICHAEL; RAO, SIDDURI ACHYUTHA. THE CHEMISTRY OF POLYFUNCTIONAL ORGANOZINC AND COPPER REAGENTS. PURE AND APPLIED CHEMISTRY 1992, 64(3), 361
  153913. 9. A REVIEWa
  153914. GABRIEL WEATHERHEAD
  153915. 7590N
  153916. 2/28/96V
  153917. REETZ, M. T. METAL, LIGAND AND PROTECTIVE GROUP TUNING AS A MEANS TO CONTROL SELECTIVITY. PURE AND APPLIED CHEMISTRY 1992, 64(3), 351
  153918. 9. A REVIEWa
  153919. GABRIEL WEATHERHEAD
  153920. 7591N
  153921. 2/28/96V
  153922. KISHI, YOSHITO. APPLICATIONS OF NICKEL(II)/CHROMIUM(II)
  153923. MEDIATED COUPLING REACTIONS TO NATURAL PRODUCTS SYNTHESES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 343
  153924. 50. A REVIEWa
  153925. GABRIEL WEATHERHEAD
  153926. 7592N
  153927. 2/28/96V
  153928. PFEFFER, MICHEL SELECTED APPLICATIONS TO ORGANIC SYNTHESIS OF INTRAMOLECULAR C
  153929. H ACTIVATION REACTIONS BY TRANSITION METALS. PURE AND APPLIED CHEMISTRY 1992, 64(3), 335
  153930. 42. A REVIEWa
  153931. GABRIEL WEATHERHEAD
  153932. 7593N
  153933. 2/28/96
  153934. NEGISHI, EIICHI. ZIPPER
  153935. MODE CASCADE CARBOMETALATION FOR CONSTRUCTION OF POLYCYCLIC STRUCTURES. PURE AND APPLIED CHEMISTRY 1992, 64(3), 323
  153936. 34. A REVIEWa
  153937. GABRIEL WEATHERHEAD
  153938. 7594N
  153939. 2/28/96VzTROST, BARRY, M. A BIOLOGICAL CATALYSIS FOR SYNTHETIC EFFICIENCY. PURE AND APPLIED CHEMISTRY 1992, 64(3), 315
  153940. 22. A REVIEWa
  153941. GABRIEL WEATHERHEAD
  153942. 7595N
  153943. 2/28/96V
  153944. LIPSHUTZ, BRUCE H.; SENGUPTA, SAUMITRA. ORGANOCOPPER REAGENTS: SUBSTITUTION, CONJUGATE ADDITION, CARBO/METALLOCUPRATION, AND OTHER REACTIONS. ORGANIC REACTIONS 1992, 41,135
  153945. 632. A REVIEWa
  153946. GABRIEL WEATHERHEAD
  153947. 7596N
  153948. 2/28/96V
  153949. HUDLICKY, TOMAS; FAN, RULIN; REED, JOSEPHINE W.; GADAMASETTI, KUMAR G. DIVINYLCYCLOPROPANE
  153950. CYCLOHEPTADIENE REARRANGEMENT. ORGANIC REACTIONS 1992,41,1
  153951. 134. A REVIEWa
  153952. GABRIEL WEATHERHEAD
  153953. 7597N
  153954. 2/28/96
  153955. STETTER, HERMANN
  153956.  KUHLMANN, HEINRICH. THE CATALYZED NUCLEOPHILIC ADDITION OF ALDEHYDES TO ELECTROPHILIC DOUBLE BOND. ORGANIC REACTIONS 1991,40,407
  153957. 496. A REVIEWa
  153958. GABRIEL WEATHERHEAD
  153959. 7598N
  153960. 2/28/96V
  153961. DE LUCCHI, OTTORINO; MIOTTI, UMBERTO; MODENA, GIORGIO. THE PUMMERER REACTION OF SULFINYL COMPOUNDS. ORGANIC REACTIONS 1991, 40, 157
  153962. 406. A REVIEWa
  153963. GABRIEL WEATHERHEAD
  153964. 7599N
  153965. 2/28/96VWPASTO, DANIEL J.; TAYLOR, RICHARD T. REDUCTION WITH DIIMIDE. 199L, 40, 91
  153966. 156. A REVIEWa
  153967. GABRIEL WEATHERHEAD
  153968. 7600N
  153969. 2/28/96V
  153970. SHORE, NEIL E. THE PAUSON
  153971. KHAND CYCLOADDITION REACTION FOR SYNTHESIS OF CYCLOPENTENONES. ORGANIC REACTIONS 1991, 40,1
  153972. 90. A REVIEWa
  153973. GABRIEL WEATHERHEAD
  153974. 7601N
  153975. 2/28/96V
  153976. SEYDEN
  153977. PENNE, J. SELECTIVE CARBANION CHEMISTRY AND ANION
  153978. CATION INTERACTIONS IN SOLUTION: A SURVEY. NEW JOURNAL OF CHEMISTRY 1992, 16(1
  153979. 2), 251
  153980. 4. A REVIEWa
  153981. GABRIEL WEATHERHEAD
  153982. 7602N
  153983. 2/28/96
  153984. 6VgRANDIC, MILAN. ORTHOGONAL MOLECULAR DESCRIPTORS. NEW JOURNAL OF CHEMISTRY 1991, 16(7), 517
  153985. 25. A REVIEWa
  153986. GABRIEL WEATHERHEAD
  153987. 7603N
  153988. 2/28/96V
  153989. DJERASSI, C.; DOSS, G. A. STRUCTURE AND BIOSYNTHESIS OF CYCLOPROPANE
  153990. CONTAINING STEROLS OF MARINE ORIGIN. NEW JOURNAL OF CHEMISTRY 1990, 14(10), 713
  153991. 19. A REVIEWa
  153992. GABRIEL WEATHERHEAD
  153993. 7604N
  153994. 2/28/96V
  153995. MARKOVSKII, L. N.; KALCHENKO, V. I.; NEGREBETSKII, V. V. AMIDINE DERIVATIVES OF HEXACOORDINATE PHOSPHORUS. NEW JOURNAL OF CHEMISTRY 1990, 14(5), 339
  153996. 51. A REVIEWa
  153997. GABRIEL WEATHERHEAD
  153998. 7605N
  153999. 2/28/96ViLEWIS, J. R. AMARYLLIDACEAE AND SCELETIUM ALKALOIDS. NATURAL PRODUCT REPORTS 1992, 9(2), 183
  154000. 91. A REVIEWa
  154001. GABRIEL WEATHERHEAD
  154002. 7606N
  154003. 2/28/96VmDEWICK, P. M. THE BIOSYNTHESIS OF SHIKIMATE METABOLITES. NATURAL PRODUCT REPORTS 1992, 9(2), 153
  154004. 81. A REVIEWa
  154005. GABRIEL WEATHERHEAD
  154006. 7607N
  154007. 2/28/96
  154008. ;VvHANSON, J. R. THE MICROBIOLOGICAL TRANSFORMATION OF DITERPENOIDS. NATURAL PRODUCT REPORTS 1992, 9(2), 139
  154009. 51. A REVIEWa
  154010. GABRIEL WEATHERHEAD
  154011. 7608N
  154012. 2/28/96V
  154013. BROWN, DEARG S.; PAQUETTE, LEO A. A SURVEY OF 6,9
  154014. EPOXYCYCLODECA[B]FURAN SESQUITERPENES. HETEROCYCLES 1992, 34(4), 807
  154015. 34. A REVIEWa
  154016. GABRIEL WEATHERHEAD
  154017. 7609N
  154018. 2/28/96V
  154019. AFARINKIA, KAMYAR. FOUR
  154020. MEMBERED HETEROCYCLES CONTAINING ONE PHOSPHORUS AND ONE OTHER HETEROATOM. HETEROCYCLES 1992, 34(2), 369
  154021. 85. A REVIEWa
  154022. GABRIEL WEATHERHEAD
  154023. 7610N
  154024. 2/28/96V
  154025. BEGTRUP, MIKAEL. A GENERAL DESCRIPTION OF THE REACTIVITY OF HETEROAROMATIC COMPOUNDS BASED ON THE DONOR
  154026. ACCEPTOR CONCEPT. HETEROCYCLES 1992, 33(2), 1129
  154027. 53. A REVIEWa
  154028. GABRIEL WEATHERHEAD
  154029. 7611N
  154030. 2/28/96V
  154031. BOCZON, WLADYSLAW. STEREOCHEMICAL ASPECTS OF BISQUINOLIZIDINE ALKALOIDS SPARTEINE TYPE. HETEROCYCLES 1992, 33(2),1101
  154032. 28. A REVIEWa
  154033. GABRIEL WEATHERHEAD
  154034. 7612N
  154035. 2/28/96
  154036. HOSOKAWA, TAKAHIRO; MURAHASHI, SHUNICHI. SYNTHESIS OF OXYGEN
  154037. CONTAINING HETEROCYCLES USING PALLADIUM(II) CATALYSTS. HETEROCYCLES 1992, 33(2), 1079
  154038. 100. A REVIEWa
  154039. GABRIEL WEATHERHEAD
  154040. 7613N
  154041. 2/28/96V
  154042. YOKOMATSU, TSUTOMU; YUASA, YOKO; SHIBUYA, SHIROSHI. SYNTHESIS OF BETA
  154043. OXYGENATED GAMMA
  154044. AMINO ACIDS AND GAMMA
  154045. OXYGENATED DELTA
  154046. AMINO ACIDS FROM ALPHA
  154047. AMINO ACIDS. HETEROCYCLES 1992, 33(2),1051
  154048. 78. A REVIEWa
  154049. GABRIEL WEATHERHEAD
  154050. 7614N
  154051. 2/28/96V
  154052. KATRITZKY, ALAN R.; LAM, JAMSHED N. HETEROCYCLIC N
  154053. OXIDES AND N
  154054. IMIDES. HETEROCYCLES HETEROCYCLES 1992, 33(2),1011
  154055. 49. A REVIEWa
  154056. GABRIEL WEATHERHEAD
  154057. 7615N
  154058. 2/28/96V
  154059. AVALOS, MARTIN; BABIANO, REYES; CINTAS, PEDRO; JIMENEZ, JOSE LUIS; PALACIOS, JUAN CARLOS. HALOALKYL ISOTHIOCYANATES, USEFUL AND VERSATILE REAGENTS IN HETEROCYCLIC CHEMISTRY. HETEROCYCLES 1992, 33(2), 973
  154060. 1010. A REVIEWa
  154061. GABRIEL WEATHERHEAD
  154062. 7616N
  154063. 2/28/96
  154064. CHUPAKHIN, 0.; ALEKSEEV, S.; RUDAKOV, B.; CHARUSHIN, V. RECENT ADVANCES IN THE CHEMISTRY OF AS
  154065. TRIAZINIUM SALTS. HETEROCYCLES 1992, 33(2), 931
  154066. 72. A REVIEWa
  154067. GABRIEL WEATHERHEAD
  154068. 7617N
  154069. 2/28/96V
  154070. YOSHIDA, TAKASHI; HATANO, TSUTOMU; KUWAJIMA, TAKAKO; OKUDA, TAKUO. OLIGOMERIC HYDROLYZABLE TANNINS
  154071. THEIR PROTON NMR SPECTRA AND PARTIAL DEGRADATION. HETEROCYCLES 1992, 33(1), 463
  154072. 82. A REVIEWa
  154073. GABRIEL WEATHERHEAD
  154074. 7618N
  154075. 2/28/96V
  154076. MORIMOTO, TOSHIAKI; CHIBA, MITSUO; ACHIWA, KAZUO. DEVELOPMENT OF MODIFIED CHIRAL DIOXOLANE BISPHOSPHINE LIGANDS AND THEIR USE IN EFFICIENT ASYMMETRIC SYNTHESIS OF NATURALLY OCCURRING LIGNANS. HETEROCYCLES 1992, 33(1), 435
  154077. 62. A REVIEWa
  154078. GABRIEL WEATHERHEAD
  154079. 7619N
  154080. 2/28/96V
  154081. TAKAYAMA, MITSUO; FUKAI, TOSHIO; HANO, YOSHIO; NOMURA, TARO. MASS SPECTROMETRY OF PRENYLATED &VONOIDS. HETEROCYCLES 1992, 33(1), 405
  154082. 34. A REVIEWa
  154083. GABRIEL WEATHERHEAD
  154084. 7620N
  154085. 2/28/96
  154086. YAMANAKA, HIROSHI. CONTRIBUTIONS OF PROFESSOR MASATOMO HAMANA IN HETEROCYCLIC CHEMISTRY. RESEARCH LIFE OF A SCIENTIST IN HETEROAROMATIC N
  154087. OXIDE CHEMISTRY. HETEROCYCLES 1992, 33(1), 1
  154088. 15. A REVIEWa
  154089. GABRIEL WEATHERHEAD
  154090. 7621N
  154091. 2/28/96V
  154092. CHELA, FLORES JULIAN. COMMENTS ON A NOVEL APPROACH TO THE ROLE OF CHIRALITY IN THE ORIGIN OF LIFE. CHIRALITY 1991, 3(5), 389
  154093. 92. A REVIEWa
  154094. GABRIEL WEATHERHEAD
  154095. 7622N
  154096. 2/28/96V~SALVADORI, PIERO; BERTUCCI, CARLO; ROSINI, CARLO. CIRCULAR DICHROISM DETECTION IN HPLC. CHIRALITY 1991, 3(4), 376
  154097. 85. A REVIEWa
  154098. GABRIEL WEATHERHEAD
  154099. 7623N
  154100. 2/28/96V
  154101. BOTTEGHI, CARLO; PAGANELLI, STEFANO; SCHIONATO, ALBERTO; MARCHETTI, MAURO. ASYMMETRIC HYDROFORMYLATION IN THE SYNTHESIS OF PHARMACEUTICALS. CHIRALITY 1991, 3(4), 355
  154102. 69. A REVIEWa
  154103. GABRIEL WEATHERHEAD
  154104. 7624N
  154105. 2/28/96
  154106. TOGNI, ANTONIO; PASTOR, STEPHEN D. COOPERATIVITY OF CHIRALITY IN HOMOGENEOUS CATALYSIS: THE GOLD(I)
  154107. CATALYZED ALDOL REACTION AND THE VANADIUM(IV)
  154108. CATALYZED HETERO
  154109. DIELS
  154110. ALDER CYCLOADDITION. CHIRALITY 1991, 3(4), 331
  154111. 40. A REVIEWa
  154112. GABRIEL WEATHERHEAD
  154113. 7625N
  154114. 2/28/96VeMASON, STEPHEN F. PREBIOTIC SOURCES OF BIOMOLECULAR HANDEDNESS. CHIRALITY 1991, 3(4), 223
  154115. 6. A REVIEWa
  154116. GABRIEL WEATHERHEAD
  154117. 7626N
  154118. 2/28/96V
  154119. TESTA, BERNARD; TRAGER, WILLIAM F. RACEMATES VERSUS ENANTIOMERS IN DRUG DEVELOPMENT: DOGMATISM OR PRAGMATISM? CHIRALITY 1990, 2(3), 129
  154120. 33. A REVIEWa
  154121. GABRIEL WEATHERHEAD
  154122. 7627N
  154123. 2/28/96
  154124. PAQUETTE, L. A. INVESTIGATIONS INTO FURANOCEMBRANOLIDE DITERPENE CONSTRUCTION. TOTAL SYNTHESIS OF DIHYDROPSEUDOPTEROLIDE, GORGIACERONE, AND ACEROSOLIDE. REVERSIBLE INTERCONVERSION OF PSEUDOPTEROLIDE AND TOBAGOLIDE. CHEMTRACTS: ORGANIC CHEMISTRY 1992, 5(3), 141. A REVIEW
  154125. GABRIEL WEATHERHEAD
  154126. 2/28/96V
  154127. MARSHALL, JAMES A. CHIRAL ALKOXYALLYLIC AND ALLENIC STANNANES AS REAGENTS FOR DIASTEREO
  154128.  AND ENANTIOSELECTIVE SYNTHESIS. CHEMTRACTS: ORGANIC CHEMISTRY 1992, 5(2), 75. A REVIEWa
  154129. GABRIEL WEATHERHEAD
  154130. 7629N
  154131. 2/28/96VeMCLAFFERTY, FRED W.; MICHNOWICZ, JOHN A. STATE
  154132. ART GC/MS. CHEMTECH 1992, 22(3),182
  154133. 9. A REVIEWa
  154134. GABRIEL WEATHERHEAD
  154135. 7630N
  154136. 2/28/96VLMARGOLIN, ALEXEY L. ENZYMES: USE THEM. CHEMTECH 1991, 21(3), 160
  154137. 7. A REVIEWa
  154138. GABRIEL WEATHERHEAD
  154139. 7631N
  154140. 2/28/96V
  154141. BANISTER, A. J.; RAWSON, J. M. DITHIADIAZOLES: A NEW FAMILY OF FREE RADICALS. CHEMISTRY IN BRITAIN 1992, 28(2),148
  154142. 52. A REVIEWa
  154143. GABRIEL WEATHERHEAD
  154144. 7632N
  154145. 2/28/96V^STODDART, FRASER. MAKING MOLECULES TO ORDER. CHEMISTRY IN BRITAIN 1991, 27(8) 714
  154146. 18. A REVIEWa
  154147. GABRIEL WEATHERHEAD
  154148. 7633N
  154149. 2/28/96
  154150. UVwPOTIER, PIERRE. SEARCH AND DISCOVERY OF NEW ANTITUMOR COMPOUNDS. CHEMICAL SOCIETY REVIEWS 1992, 21(2), 113
  154151. 19. A REVIEWa
  154152. GABRIEL WEATHERHEAD
  154153. 7634N
  154154. 2/28/96V\WALTON, JOHN C. BRIDGEHEAD RADICALS. CHEMICAL SOCIETY REVIEWS 1992, 21(2), 105
  154155. 112. A REVIEWa
  154156. GABRIEL WEATHERHEAD
  154157. 7635N
  154158. 2/28/96V
  154159. BUTLER, ANTHONY R.; WU, YU
  154160. LIN. ARTEMISININ (QINGHAOSU). A NEW TYPE OF ANTIMALARIAL DRUG. CHEMICAL SOCIETY REVIEWS 1992, 21(2), 85
  154161. 90. A REVIEWa
  154162. GABRIEL WEATHERHEAD
  154163. 7636N
  154164. 2/28/96V
  154165. ESCHENMOSER, ALBERT; LEOWENTHAL, E. I. CHEMISTRY OF POTENTIALLY PREBIOLOGICAL NATURAL PRODUCTS. CHEMICAL SOCIETY REVIEWS 1992, 21(1),1
  154166. 16. A REVIEWa
  154167. GABRIEL WEATHERHEAD
  154168. 7637N
  154169. 2/28/96V
  154170. WILKINSON, JOHN A. RECENT ADVANCES IN THE SELECTIVE FORMATION OF THE CARBON
  154171. FLUORINE BOND. CHEMICAL REVIEWS 1992, 92(4), 505
  154172. 19. A REVIEWa
  154173. GABRIEL WEATHERHEAD
  154174. 7638N
  154175. 2/28/96
  154176. WIEGAND, BENJAMIN C.; FRIEND, CYNTHIA M. MODEL STUDIES OF THE DESULFURIZATION REACTIONS ON METAL SURFACES AND IN ORGANOMETALLIC COMPLEXES. CHEMICAL REVIEWS 1992, 92(4), 491
  154177. 504. A REVIEWa
  154178. GABRIEL WEATHERHEAD
  154179. 7639N
  154180. 2/28/96VlMANDER, LEWIS N. THE CHEMISTRY OF GIBBERELLINS: AN OVERVIEW. CHEMICAL REVIEWS 1992, 92(4), 573
  154181. 612. A REVIEWa
  154182. GABRIEL WEATHERHEAD
  154183. 7640N
  154184. 2/28/96
  154185. JORDAN, KENNETH D.; PADDON
  154186. ROW, MICHAEL N. ANALYSIS OF THE INTERACTIONS RESPONSIBLE FOR LONG
  154187. RANGE THROUGHBOND
  154188. MEDIATED ELECTRONIC COUPLING BETWEEN REMOTE CHROMOPHORES ATTACHED TO RIGID POLYNORBORNYL BRIDGES. CHEMICAL REVIEWS 1992, 92(3), 395
  154189. 410. A REVIEW
  154190. GABRIEL WEATHERHEAD
  154191. 7641N
  154192. 2/28/96VyBRAGA, DARIO. DYNAMICAL PROCESSES IN CRYSTALLINE ORGANOMETALLIC COMPLEXES. CHEMICAL REVIEWS 1992, 92(4), 633
  154193. 65. A REVIEWa
  154194. GABRIEL WEATHERHEAD
  154195. 7642N
  154196. 2/28/96
  154197. AN, HAOYUN; BRADSHAW, JERALD S.; IZATT, REED M. MACROPOLYCYCLIC POLYETHERS (CAGES) AND RELATED COMPOUNDS. CHEMICAL REVIEWS 1992, 92(4), 543
  154198. 72. A REVIEWa
  154199. GABRIEL WEATHERHEAD
  154200. 7643N
  154201. 2/28/96VuBOHLMANN, ROLF. THE FOLDING OF SQUALENE: AN OLD PROBLEM HAS NEW RESULTS. ANG CHEM INT ED 1992, 31(5), 582
  154202. 4. A REVIEWa
  154203. GABRIEL WEATHERHEAD
  154204. 7644N
  154205. 2/28/96V
  154206. KAUPP, GERD. [4 + 4]
  154207. CYCLOADDITION REACTION IN THE TOTAL SYNTHESIS OF EIGHT MEMBERED RING CONTAINING NATURAL PRODUCTS. ANG CHEM INT ED 1992, 31(4), 422
  154208. 4. A REVIEWa
  154209. GABRIEL WEATHERHEAD
  154210. 7645N
  154211. 2/28/96V
  154212. STEINBORN, DIRK. ON THE INFLUENCE OF HETEROATOMS IN ALPHA AND BETA
  154213. FUNCTIONALIZED ALKYL TRANSITION METAL COMPOUNDS. ANG CHEM INT ED 1992, 31(4), 401
  154214. 21. A REVIEWa
  154215. GABRIEL WEATHERHEAD
  154216. 7646N
  154217. 2/28/96V
  154218. JUNG, GUENTHER; BECK
  154219. SICKINGER, ANNETTE G. MULTIPLE PEPTIDE SYNTHESIS METHODS AND THEIR APPLICATIONS. ANG CHEM INT ED 1992, 31(4), 367
  154220. 83. A REVIEW
  154221. GABRIEL WEATHERHEAD
  154222. 7647N
  154223. 2/28/96VgJANOSCHEK, RUDOLF. STRUCTURES, STRUCTURES, AND STRUCTURES. ANG CHEM INT ED 1992, 31(3), 290
  154224. 2. A REVIEWa
  154225. GABRIEL WEATHERHEAD
  154226. 7648N
  154227. 2/28/96V
  154228. REISSIG, HANS
  154229. ULRICH. SUGARS AS CHIRAL AUXILIARIES FOR THE SYNTHESIS OF ENANTIOMERICALLY PURE COMPOUNDS. ANG CHEM INT ED 1992, 31(3), 288
  154230. 90. A REVIEWa
  154231. GABRIEL WEATHERHEAD
  154232. 7649N
  154233. 2/28/96VdMAYER, JAMES M. BOND
  154234. STRETCH ISOMERS. FACT OR ARTIFACT? ANG CHEM INT ED 1992, 31(3), 286
  154235. 7. A REVIEWa
  154236. GABRIEL WEATHERHEAD
  154237. 7650N
  154238. 2/28/96VmSTANG, PETER J. ALKYNYL
  154239.  AND ALKENYL(PHENYL)IODONIUM COMPOUNDS. ANG CHEM INT ED 1992, 31(3), 274
  154240. 85. A REVIEWa
  154241. GABRIEL WEATHERHEAD
  154242. 7651N
  154243. 2/28/96V
  154244. WADEPOHL, HUBERT. BENZENE AND ITS DERIVATIVES AS BRIDGING LIGANDS IN TRANSITION METAL COMPLEXES. ANG CHEM INT ED 1992, 31(3), 247
  154245. 62. A REVIEWa
  154246. GABRIEL WEATHERHEAD
  154247. 7652N
  154248. 2/28/96
  154249. KROTO, HAROLD W. C60. BUCKMINSTERFULLERENE, THE CELESTIAL SPHERE THAT FELL TO EARTH. ANG CHEM INT ED 1992, 31(2),111
  154250. 29. A REVIEWa
  154251. GABRIEL WEATHERHEAD
  154252. 7653N
  154253. 2/28/96V
  154254. LEE, T. RANDALL; WHITESIDES, GEORGE M. HETEROGENEOUS, PLATINUM
  154255. CATALYZED HYDROGENATIONS OF (DIOLEFIN)DIALKYLPLATINUM(II) COMPLEXES. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(6), 266
  154256. 72. A REVIEWa
  154257. GABRIEL WEATHERHEAD
  154258. 7654N
  154259. 2/28/96V
  154260. YOON, UNG CHAN; MARIANO, PATRICK S. MECHANISTIC AND SYNTHETIC ASPECTS OF AMINE
  154261. ENONE SINGLE ELECTRON TRANSFER. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(5), 233
  154262. 40. A REVIEWa
  154263. GABRIEL WEATHERHEAD
  154264. 7655N
  154265. 2/28/96VyESPENSON, JAMES H. CHEMISTRY OF ORGANOCHROMIUM(III) COMPLEXES. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(5), 222
  154266. 7. A REVIEWa
  154267. GABRIEL WEATHERHEAD
  154268. 7656N
  154269. 2/28/96
  154270. BEAK, PETER. DETERMINATIONS OF TRANSITION
  154271. STATE GEOMETRIES BY THE ENDOCYCLIC RESTRICTION TEST: MECHANISMS OF SUBSTITUTION AT NONSTEREOGENIC ATOMS. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(5), 215
  154272. 22. A REVIEWa
  154273. GABRIEL WEATHERHEAD
  154274. 7657N
  154275. 2/28/96V
  154276. JOHNSON, ROBERT D.; BETHUNE, DONALD S.; YANNONI, COSTANTINO, S. FULLERENE STRUCTURE AND DYNAMICS: A MAGNETIC RESONANCE POTPOURRI. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(3),169
  154277. 75. A REVIEWa
  154278. GABRIEL WEATHERHEAD
  154279. 7658N
  154280. 2/28/96V
  154281. MCELVANY, STEPHEN W.; ROSS, MARK M.
  154282.  CALLAHAN, JOHN H. CHARACTERIZATION OF FULLERENES BY MASS SPECTROMETRY. ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(3), 162
  154283. 8. A REVIEWa
  154284. GABRIEL WEATHERHEAD
  154285. 7659N
  154286. 2/28/96V
  154287. DIEDERICH, FRANCOIS; WHETTEN, ROBERT L. BEYOND C60: THE HIGHER FULLERENES.  ACCOUNTS OF CHEMICAL RESEARCH 1992, 25(3),119
  154288. 26. A REVIEWa
  154289. GABRIEL WEATHERHEAD
  154290. 7660N
  154291. 2/28/96
  154292. pVLSMALLEY, R. E. SELF
  154293. ASSEMBLY OF THE FULLERENES 1992, 25(3), 98
  154294. 105. A REVIEWa
  154295. GABRIEL WEATHERHEAD
  154296. 7661N
  154297. 2/28/96V
  154298. DJERASSI, CARL; SILVA, CHRISTOPHER, J. SPONGE STEROLS: ORIGINS AND BIOSYNTHESIS ACCOUNTS OF CHEMICAL RESEARCH 1991, 24(12), 371
  154299. 78. A REVIEWa
  154300. GABRIEL WEATHERHEAD
  154301. 7662N
  154302. 2/28/96VsTROST BARRY; FLEMING, I., EDS. COMPREHENSIVE ORGANIC SYNTHESIS. VOLS. 1
  154303. 9. PERGAMON: OXFORD, U.K., 1991.   A REVIEWa
  154304. GABRIEL WEATHERHEAD
  154305. 7663N
  154306. 2/28/96VkTOWNSEND, LEROY B., ED. CHEMISTRY OF NUCLEOSIDES AND NUCLEOTIDES, VOL. 2. PLENUM: NEW YORK, 1991.  A REVIEWa
  154307. GABRIEL WEATHERHEAD
  154308. 7664N
  154309. 2/28/96VMSZEPESI, GABOR. HOW TO USE REVERSE
  154310. PHASE HPLC. VCH: NEW YORK, 1992.  A REVIEWa
  154311. GABRIEL WEATHERHEAD
  154312. 7665N
  154313. 2/28/96VzSEYDEN
  154314. PENNE, JACQUELINE. REDUCTIONS BY THE ALUMINO
  154315.  AND BOROHYDRIDES IN ORGANIC SYNTHESIS. VCH: NEW YORK, 1991.  A REVIEWa
  154316. GABRIEL WEATHERHEAD
  154317. 7666N
  154318. 2/28/96VUSCUDDER, PAUL H. ELECTRON FLOW IN ORGANIC CHEMISTRY. WILEY: NEW YORK, 1992.  A REVIEWa
  154319. GABRIEL WEATHERHEAD
  154320. 7667N
  154321. 2/28/96VxRAHMAN, ATTA
  154322. UR. 13C
  154323. NMR OF NATURAL PRODUCTS. VOL. 1. MONOTERPENES AND SESQUITERPENES. PLENUM: NEW YORK, 1992.  A REVIEWa
  154324. GABRIEL WEATHERHEAD
  154325. 7668N
  154326. 2/28/96V
  154327. NOELS, A. F.; GRAZIANI, M.; HUBERT, A. J., EDS. CATALYSIS BY METAL COMPLEXES, VOL. 12: METAL PROMOTED SELECTIVITY. KLUWER: DORDRECHT, THE NETHERLANDS, 1991.  A REVIEWa
  154328. GABRIEL WEATHERHEAD
  154329. 7669N
  154330. 2/28/96V
  154331. MOTHERWELL, WILLIAM B.; CRICH DAVID. FREE
  154332. RADICAL CHAIN REACTIONS IN ORGANIC CHEMISTRY. ACADEMIC: SAN DIEGO, CA, 1991.  A REVIEWa
  154333. GABRIEL WEATHERHEAD
  154334. 7670N
  154335. 2/28/96VnMEHROTRA, R. C. SINGH, ANIRUDH. ORGANOMETALLIC CHEMISTRY. A UNIFIED APPROACH. WILEY: NEW YORK, 1991.  A REVIEWa
  154336. GABRIEL WEATHERHEAD
  154337. 7671N
  154338. 2/28/96
  154339. LAMBERT JOSEPH B.; TAKEUCHI, YOSHITO, EDS. CYCLIC ORGANONITROGEN STEREODYNAMICS (METHODS IN STEREOCHEMICAL ANALYSIS). VCH: NEW YORK, 1992.   A REVIEWa
  154340. GABRIEL WEATHERHEAD
  154341. 7672N
  154342. 2/28/96V
  154343. LAMBERT, JOSEPH B.; TAKEUCHI, YOSHITO, EDS. ACYCLIC ORGANONITROGEN STEREODYNAMICS (METHODS IN STEREOCHEMICAL ANALYSIS). VCH: NEW YORK, 1992.  A REVIEWa
  154344. GABRIEL WEATHERHEAD
  154345. 7673N
  154346. 2/28/96V
  154347. FUJIHARA, HISASHI; FURUKAWA, NAOMICHI. DISULFIDE DI
  154348.  CATIONS FROM CYCLIC BIS
  154349. SULFIDES.   REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154350. GABRIEL WEATHERHEAD
  154351. 7674N
  154352. 2/28/96V
  154353. PADWA, ALBERT; MURPHREE, S. SHAUN. CYCLOADDITION AND CYCLIZATION REACTIONS OF UNSATURATED SULFONES IN ORGANIC SYNTHESIS. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154354. GABRIEL WEATHERHEAD
  154355. 7675N
  154356. 2/28/96
  154357. SATOH, TSUYOSHI; YAMAKAWA, KOJI. ORGANIC SYNTHESIS WITH SULFINYLOXIRANES AND SULFONYLOXIRANES. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154358. GABRIEL WEATHERHEAD
  154359. 7676N
  154360. 2/28/96
  154361. ,ARAI, YOSHITSUGU; KOIZUMI, TORU. SYNTHESIS AND ASYM
  154362.  METRIC DIELS
  154363. ALDER REACTIONS OF CHIRAL  ALPHA,BETA
  154364. UNSATURATED SULFOXIDES BEARING A 2
  154365. HYDROXY
  154366. BORNYL GROUP AS AN EFFICIENT LIGAND ON THE SULFUR CENTER. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEW
  154367. GABRIEL WEATHERHEAD
  154368. 7677N
  154369. 2/28/96V
  154370. NEGISHI, EI
  154371. ICHI; TAKAHASHI, TAMOTSU. ZIRCONOCENE
  154372.  ALKENE COMPLEXES: THEIR FORMATION, STRUCTURE, AND REACTIONS. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154373. GABRIEL WEATHERHEAD
  154374. 7678N
  154375. 2/28/96
  154376. HISATOME, MASAO. [M]FERROCENOPHANES AND MULTI
  154377.  BRIDGED [MN]FERROCENOPHANES. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154378. GABRIEL WEATHERHEAD
  154379. 7679N
  154380. 2/28/96
  154381. MONTANARI, FERNANDO; BANFI, STEFANO; POZZI, GIANLUCA; QUICI, SILVIO. DESIGN OF CHEMICALLY ROBUST METALLO
  154382. PORPHYRINS AS EFFICIENT BIOMIMETIC CATALYSTS IN OXYGENATION REACTIONS. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEW
  154383. GABRIEL WEATHERHEAD
  154384. 7680N
  154385. 2/28/96V
  154386. TACHIBANA, AKIMOTO; KAWAUCHI, SUSUMU YAMABE, TOKIO. THE BOND NATURE AND REACTIVITY OF SILICON COMPOUNDS. REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154387. GABRIEL WEATHERHEAD
  154388. 7681N
  154389. 2/28/96
  154390. HORVATH, ARI L. MOLECULAR DESIGN. CHEMICAL STRUCTURE GENERATION FROM THE PROPERTIES OF PURE ORGANIC COMPOUNDS (STUDIES IN PHYSICAL AND THEORETICAL CHEMISTRY, VOL. 75). ELSEVIER: AMSTERDAM, 1992.   A REVIEWa
  154391. GABRIEL WEATHERHEAD
  154392. 7682N
  154393. 2/28/96V]HOLLAND, HERBERT L. ORGANIC SYNTHESIS WITH OXIDATIVE ENZYMES. VCH: NEW YORK, 1991.   A REVIEWa
  154394. GABRIEL WEATHERHEAD
  154395. 7683N
  154396. 2/28/96
  154397. HEFTMANN, ERICH, ED. CHROMATOGRAPHY, 5TH. ED. FUN
  154398.  DAMENTALS AND APPLICATIONS OF CHROMATOGRAPHY AND RELATED DIFFERENTIAL MIGRATION METHODS, PT. A FUNDAMENTALS AND TECHNIQUES (JOURNAL OF CHROMATOGRAPHY LIBRARY, VOL. 51A). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1992.  A REVIEW
  154399. GABRIEL WEATHERHEAD
  154400. 7684N
  154401. 2/28/96V
  154402. ELSCHENBROICH, CHRISTOPH.; SALZER, ALBRECHT. ORGANO
  154403.  METALLICS. A CONCISE INTRODUCTION, 2ND ED. VCH: WEINHEIM, FRG, 1992.  A REVIEWa
  154404. GABRIEL WEATHERHEAD
  154405. 7685N
  154406. 2/28/96
  154407. DESMURS, JEAN ROGER; GERARD, BERNARD EDS. ADVANCES IN ORGANOBROMINE CHEMISTRY I (INDUSTRIAL CHEMISTRY LIBRARY, VOL. 3). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1991.  A REVIEWa
  154408. GABRIEL WEATHERHEAD
  154409. 7686N
  154410. 2/28/96V
  154411. CLEMENT, R. E.; SIU, K. W. M.; HILL, HERBERT H., JR., EDS. INSTRUMENTATION FOR TRACE ORGANIC MONITORING. LEWIS: CHELSEA, MI 1992.  A REVIEWa
  154412. GABRIEL WEATHERHEAD
  154413. 7687N
  154414. 2/28/96VfAPSIMON, JOHN, ED. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOLUME 8. WILEY: NEW YORK, 1992.  A REVIEWa
  154415. GABRIEL WEATHERHEAD
  154416. 7688N
  154417. 2/28/96V
  154418. ARMITAGE, D. A. THE SILICON
  154419. HETEROATOM BOND (UPDATES FROM THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: NEW YORK, 1991.  A REVIEWa
  154420. GABRIEL WEATHERHEAD
  154421. 7689N
  154422. 2/28/96
  154423. GOLOLOBOV, YURI G.; BALITSKY, YURI V. 
  154424. AMINOCARBONYL AND RELATED COMPOUNDS IN THE SYNTHESES OF THE DERIVATIVES OF 1,3,2
  154425. OXAZAPHOSPHOLE.  REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154426. GABRIEL WEATHERHEAD
  154427. 7690N
  154428. 2/28/96V
  154429. MATHEY, FRANCOIS. A DECADE OF RESEARCH IN PHOSPHIN  IMINE CHEMISTRY.   REV ON HETEROATOM CHEM VOL 6, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1992.   A REVIEWa
  154430. GABRIEL WEATHERHEAD
  154431. 7691N
  154432. 2/28/96V
  154433. DOLBIER, WILLIAM R. CYCLOADDITIONS OF ALLENES. REACTIONS OF UNUSUAL MECHANISTIC PERSPECUITY. ADVANCES IN DETAILED REACTION MECHANISMS.  A REVIEWa
  154434. GABRIEL WEATHERHEAD
  154435. 7692N
  154436. 2/28/96V
  154437. EASTON, CHRISTOPHER J. CARBON
  154438. CENTERED RADICALS FROM AMINO ACIDS AND THEIR DERIVATIVES.  ADVANCES IN DETAILED REACTION MECHANISMS.  A REVIEWa
  154439. GABRIEL WEATHERHEAD
  154440. 7693N
  154441. 2/28/96
  154442. DAVIS, MICHAEL J.; GILBERT, BRICE C. FREE RADICAL RE  ACTIONS: FRAGMENTATION AND REARRANGEMENT IN AQUEOUS SOLUTIONS ADVANCES IN DETAILED REACTION MECHANISMS.  A REVIEWa
  154443. GABRIEL WEATHERHEAD
  154444. 7694N
  154445. 2/28/96V
  154446. NEWCOMB, MARTIN. RADICAL KINETICS AND MECHANISTIC PROBE STUDIES.  ADVANCES IN DETAILED REACTION MECHANISMS.  VOLUME 1, RADICAL, SINGLE ELECTRON TRANSFERS AND CONCERTED REACTIONS JAMES M. COXON, ED., JAI PRESS: GREENWICH, CT, 1991.   A REVIEWa
  154447. GABRIEL WEATHERHEAD
  154448. 7695N
  154449. 2/28/96
  154450. SONAWANE, HARIKISAN R.; BELLUR, NANJUNDIAH S.; AHUJA, JAIMALA R.; KULKARNI, DILIP G. RECENT DEVELOPMENTS IN THE SYNTHESIS OF OPTICALLY ACTIVE LY
  154451. ARYLPROPANOIC ACIDS: AN IMPORTANT CLASS OF NON
  154452. STEROIDAL ANTI
  154453. INFLAMMATORY AGENTS. TETRAHEDRON: ASYMMETRY 1992, 3(2), 163
  154454. 92.  A REVIEW
  154455. GABRIEL WEATHERHEAD
  154456. 7696N
  154457. 2/28/96
  154458. BLASER, HANS ULRICH. ENANTIOSELECTIVE SYNTHESIS USING CHIRAL HETEROGENEOUS CATALYSTS. TETRAHEDRON: ASYMMETRY 1991, 2(9), 843
  154459. 66.  A REVIEWa
  154460. GABRIEL WEATHERHEAD
  154461. 7697N
  154462. 2/28/96V|XIE, ZHUO FENG. PSEUDOMONAS FLUORESCENS LIPASE IN ASYMMETRIC SYNTHESIS. TETRAHEDRON: ASYMMETRY 1991, 2(8), 733
  154463. 50.  A REVIEWa
  154464. GABRIEL WEATHERHEAD
  154465. 7698N
  154466. 2/28/96V
  154467. BURGESS, VICKY A.; DAVIES, STEPHEN G.; SKERLJ, RENATO T. NADH MIMICS FOR THE STEREOSELECTIVE REDUCTION OF BENZOYLFORMATES TO THE CORRESPONDING MANDELATES. TETRAHEDRON: ASYMMETRY 1991, 2(5),299
  154468. 328.  A REVIEWa
  154469. GABRIEL WEATHERHEAD
  154470. 7699N
  154471. 2/28/96V
  154472. COX, PAUL J.; SIMPKINS, NIGEL S. ASYMMETRIC SYNTHESIS USING HOMOCHIRAL LITHIUM AMIDE BASES. TETRAHEDRON: ASYMMETRY 1991, 2(1),1
  154473. 26.  A REVIEWa
  154474. GABRIEL WEATHERHEAD
  154475. 7700N
  154476. 2/28/96
  154477. BRAVO, PIERFRANCESCO; RESNATI, GUISEPPE. PREPARATION AND PROPERTIES OF CHIRAL FLUOROORGANIC COMPOUNDS. TETRAHEDRON: ASYMMETRY 1990, 1(10),661
  154478. 92.  A REVIEWa
  154479. GABRIEL WEATHERHEAD
  154480. 7701N
  154481. 2/28/96V
  154482. ALEXAKIS, ALEXANDRE; MANGENEY, PIERRE. CHIRAL ACETALS IN ASYMMETRIC SYNTHESIS. TETRAHEDRON: ASYMMETRY 1990,1(8), 477
  154483. 511.  A REVIEWa
  154484. GABRIEL WEATHERHEAD
  154485. 7702N
  154486. 2/28/96VzGOLOLOBOV, YU. G.; KASUKHIN, L. F. RECENT ADVANCES IN THE STAUDINGER REACTION. TETRAHEDRON 1992, 48(8),1353
  154487. 406.  A REVIEWa
  154488. GABRIEL WEATHERHEAD
  154489. 7703N
  154490. 2/28/96V
  154491. COLOMBO MARIA I.; ZINCZUK, JUAN; RUVEDA, EDMUNDO A. SYNTHETIC ROUTES TO FORSKOLIN. TETRAHEDRON 1992, 48(6), 963
  154492. 1037.  A REVIEWa
  154493. GABRIEL WEATHERHEAD
  154494. 7704N
  154495. 2/28/96V~BORTHWICK, ALAN D.; BIGGADIKE, KEITH. SYNTHESIS OF CHIRAL CARBOCYCLIC NUCLEOSIDES. TETRAHEDRON 1992, 48(4), 517
  154496. 623.  A REVIEWa
  154497. GABRIEL WEATHERHEAD
  154498. 7705N
  154499. 2/28/96
  154500. BURTON, DONALD J.; YANG, ZHEN YU. FLUORINATED ORGANOMETALLICS: PERFLUOROALKYL AND FUNCTIONALIZED PERFLUOROALKYL ORGANOMETALLIC REAGENTS IN ORGANIC SYNTHESIS. TETRAHEDRON L992,48(2),189
  154501. 275.  A REVIEWa
  154502. GABRIEL WEATHERHEAD
  154503. 7706N
  154504. 2/28/96V
  154505. RUFFOLO, ROBERT R., JR. CHIRALITY IN ALPHA
  154506.  AND BETA
  154507. ADRENOCEPTOR AGONISTS AND ANTAGONISTS. TETRAHEDRON 1991, 47(48), 9953
  154508. 80.  A REVIEWa
  154509. GABRIEL WEATHERHEAD
  154510. 7707N
  154511. 2/28/96V
  154512. ROMO, DANIEL; MEYERS, A. I. CHIRAL NON
  154513. RACEMIC BICYCLIC LACTAMS. VEHICLES FOR THE CONSTRUCTION OF NATURAL AND UNNATURAL PRODUCTS CONTAINING QUATERNARY CARBON. TETRAHEDRON 1991, 47(46),9503
  154514. 69.  A REVIEWa
  154515. GABRIEL WEATHERHEAD
  154516. 7708N
  154517. 2/28/96VsEVANS, P. ANDREW; HOLMES, ANDREW B. MEDIUM RING NITROGEN HETEROCYCLES. TETRAHEDRON 1991, 47(44), 9131
  154518. 66.  A REVIEWa
  154519. GABRIEL WEATHERHEAD
  154520. 7709N
  154521. 2/28/96
  154522. JOULLIE, MADELEINE M.; THOMPSON, TRACY R. NINHYDRIN AND NINHYDRIN ANALOGS. SYNTHESES AND APPLICATIONS. TETRAHEDRON 1991, 47(42), 8791
  154523. 830.  A REVIEWa
  154524. GABRIEL WEATHERHEAD
  154525. 7710N
  154526. 2/28/96V
  154527. VAN DER STEEN, FRED H.; VAN KOTEN, GERARD. SYNTHESES OF 3
  154528. AMINO
  154529. AZETIDINONES: A LITERATURE SURVEY. 19GL, 47(36), 7503
  154530. 24.  A REVIEWa
  154531. GABRIEL WEATHERHEAD
  154532. 7711N
  154533. 2/28/96V
  154534. BOLAND, WILHELM; FROESSL, CHRISTIAN; LORENZ, MICHAEL. ESTEROLYTIC AND LIPOLYTIC ENZYMES IN ORGANIC SYNTHESIS. SYNTHESIS 1991, (12), 1049
  154535. 72.  A REVIEWa
  154536. GABRIEL WEATHERHEAD
  154537. 7712N
  154538. 2/28/96V
  154539. PETRAGNANI, N.; COMASSETO, J. V. TELLURIUM REAGENTS IN ORGANIC SYNTHESIS; RECENT ADVANCES. PART 2. SYNTHESIS 1991, (11), 897
  154540. 919.  A REVIEWa
  154541. GABRIEL WEATHERHEAD
  154542. 7713N
  154543. 2/28/96
  154544. LITTLE, R. DANIEL; MASJEDIZADEH, MOHAMMAD R.; MOELLER, KEVIN D.; DANNECKER, DOERIG INGEBORG. FACTORS AFFECTING REGIOSELECTIVITY IN THE INTRAMOLECULAR DIYL TRAPPING REACTION. SYNLETT 1992, (2), 107
  154545. 13.  A REVIEWa
  154546. GABRIEL WEATHERHEAD
  154547. 7714N
  154548. 2/28/96V
  154549. KOTSUKI, HIYOSHIZO. BICYCLIC KETALS: VERSATILE INTERMEDIATES FOR THE STEREOCONTROLLED CONSTRUCTION OF CYCLIC ETHER DERIVATIVES. SYNLETT L992, (2), 97
  154550. 106.  A REVIEWa
  154551. GABRIEL WEATHERHEAD
  154552. 7715N
  154553. 2/28/96V
  154554. DOXSEE, KENNETH, M.; MOUSER, JOHN K. M.; FARAHI, JUDAH B. TITANIUM METALLACYCLES AS INTERMEDIATES IN THE SYNTHESIS OF ACYCLIC AND HETEROCYCLIC COMPOUNDS. SYNLETT L992, (1),13
  154555. 21.  A REVIEWa
  154556. GABRIEL WEATHERHEAD
  154557. 7716N
  154558. 2/28/96V
  154559. THUMMEL, RANDOLPH P. THE APPLICATION OF FRIEDLANDER AND FISCHER METHODOLOGIES TO THE SYNTHESIS OF ORGANIZED POLYAZA CAVITIES. SYNLETT L992, (1),1
  154560. 12.  A REVIEWa
  154561. GABRIEL WEATHERHEAD
  154562. 7717N
  154563. 2/28/96
  154564. HATANAKA, YASUO; HIYAMA, TAMEJIRO. HIGHLY SELECTIVE CROSS
  154565. COUPLING REACTIONS OF ORGANOSILICON COMPOUNDS MEDIATED BY FLUORIDE ION AND A PALLADIUM CATALYST. SYNLETT L99L, (12), 845
  154566. 53.  A REVIEWa
  154567. GABRIEL WEATHERHEAD
  154568. 7718N
  154569. 2/28/96V
  154570. BARRETT, ANTHONY G. M.; HILL, JASON M.; WALLACE, ELI M.; FLYGARE, JOHN A. RECENT STUDIES ON THE PETERSON OLEFINATION REACTION. SYNLETT L99L, (11), 764
  154571. 70.  A REVIEWa
  154572. GABRIEL WEATHERHEAD
  154573. 7719N
  154574. 2/28/96V
  154575. BRUNEAU, CHRISTIAN; NEVEUX, MURIEL; KABOUCHE, ZAHIA; RUPPIN, CHRISTOPHE; DIXNEUF, PIERRE H. RUTHENIUM
  154576. CATALYZED ADDITIONS TO ALKYNES: SYNTHESIS OF ACTIVATED ESTERS AND THEIR USE IN ACYLATION REACTIONS. SYNLETT L99L, (11), 755
  154577. 63.  A REVIEWa
  154578. GABRIEL WEATHERHEAD
  154579. 7720N
  154580. 2/28/96VwSIEBERT, W. FROM SANDWICH AND TRIPLE
  154581. DECKER TO ORGANOMETALLIC POLYMERS. RUSSIAN CHEM REV L99L, 60(7), 784
  154582. 91.  A REVIEWa
  154583. GABRIEL WEATHERHEAD
  154584. 7721N
  154585. 2/28/96
  154586. VkABDULGANEVA, S. A.; ERZHANOV, K. B. ACETYLENIC AMINO ACIDS. RUSSIAN CHEM REV L99L, 60(6), 676
  154587. 88.  A REVIEWa
  154588. GABRIEL WEATHERHEAD
  154589. 7722N
  154590. 2/28/96V
  154591. LAKHVICH, F. A.; KHRIPACH, V. A.; ZHABINSKII, V. N. SYNTHESIS OF BRASSINOSTEROIDS: A NEW CLASS OF GROWTH HORMONES. RUSSIAN CHEM REV L991, 60(6), 658
  154592. 75.  A REVIEWa
  154593. GABRIEL WEATHERHEAD
  154594. 7723N
  154595. 2/28/96V
  154596. MOISEENKOV, A. M.; DRAGAN, V. A.; VESELOVSKII, V. V. SYNTHETIC APPLICATION OF THE PUMMERER REACTION. RUSSIAN CHEM REV L99L, 60(6), 643
  154597. 57.  A REVIEWa
  154598. GABRIEL WEATHERHEAD
  154599. 7724N
  154600. 2/28/96V
  154601. ORLINKOV, A. V.; AKHREM, I. S.; VOL'PIN, M. E. THE STRUCTURE OF EQUIMOLAR COMPLEXES OF ACID HALIDES WITH LEWIS ACIDS. RUSSIAN CHEM REV L99L, 60(5), 524
  154602. 38.  A REVIEWa
  154603. GABRIEL WEATHERHEAD
  154604. 7725N
  154605. 2/28/96VoTURBANOVA, E. S.; PETROV, A. A. PERFLUOROALKYL(ARYL)ACETYLENES. RUSSIAN CHEM REV L99L, 60(5), 501
  154606. 23.  A REVIEWa
  154607. GABRIEL WEATHERHEAD
  154608. 2/28/96V
  154609. MIKAYA, A. I.; VARLAMOV, A. V.; ZAIKIN, V. G.; PROSTAKOV, N. S. MASS SPECTROMETRY OF DERIVATIVES AND HETEROCYCLIC ANALOGS OF 9,10
  154610. DIHYDROANTHRACENE. RUSSIAN CHEM REV L99L, 60(5), 489
  154611. 500.  A REVIEWa
  154612. GABRIEL WEATHERHEAD
  154613. 7727N
  154614. 2/28/96V
  154615. KISLENKO, V. N.; BERLIN, A. A. KINETICS AND MECHANISM OF THE OXIDATION OF ORGANIC COMPOUNDS BY HYDROGEN PEROXIDE. RUSSIAN CHEM REV 1991, 60(5), 470
  154616. 88.  A REVIEWa
  154617. GABRIEL WEATHERHEAD
  154618. 7728N
  154619. 2/28/96V
  154620. BREN', V. A.; DUBONOSOV, A. D.; MINKIN, V. I.; CHERNOIVANOV, V. A. NORBORNADIENE
  154621. QUADRICYCLANE
  154622. AN EFFECTIVE MOLECULAR SYSTEM FOR THE STORAGE OF SOLAR ENERGY. RUSSIAN CHEM REV L99L, 60(5), 451
  154623. 69.  A REVIEWa
  154624. GABRIEL WEATHERHEAD
  154625. 7729N
  154626. 2/28/96
  154627. NEFEDOV, O. M.; EGOROV, M. P.; IOFFE, A. I.; MENCHIKOV, L. G.; ZUEV, P. S.; MINKIN, V. I.; SIMKIN, B. YA.; GLUKHOVTSEV, M. N. CRITICAL COMPILATION OF PHYSICAL PROPERTIES OF SHORT
  154628. LIVED INTERMEDIATES. CARBENES AND CARBENE ANALOGS. PURE AND AP CHEM L992, 64(2), 265
  154629. 314.  A REVIEW
  154630. GABRIEL WEATHERHEAD
  154631. 7730N
  154632. 2/28/96VrMURRAY, R. D. H. NATURALLY OCCURRING PLANT COUMARINS. PROG IN THE CHEM OF ORG NAT PROD 1991, 58, 83
  154633. 316.  A REVIEWa
  154634. GABRIEL WEATHERHEAD
  154635. 7731N
  154636. 2/28/96V
  154637. ROBINSON, J. A. CHEMICAL AND BIOLOGICAL ASPECTS OF POLYETHER
  154638. IONOPHORE ANTIBIOTIC BIOSYNTHESIS. PROG IN THE CHEM OF ORG NAT PROD L991, 58,1
  154639. 81.  A REVIEWa
  154640. GABRIEL WEATHERHEAD
  154641. 7732N
  154642. 2/28/96V[PETTIT, G. R. THE BRYOSTATINS. PROG IN THE CHEM OF ORG NAT PROD L99L, 57,153
  154643. 195.  A REVIEWa
  154644. GABRIEL WEATHERHEAD
  154645. 7733N
  154646. 2/28/96
  154647. VxCHAKRABORTY, D. P.; ROY, SHYAMALI. CARBAZOLE ALKALOIDS III. PROG IN THE CHEM OF ORG NAT PROD 199L, 57, 71
  154648. 152.  A REVIEWa
  154649. GABRIEL WEATHERHEAD
  154650. 7734N
  154651. 2/28/96
  154652. METZGER, P.; LARGEAU, C.; CASADEVALL, E. LIPIDS AND MACROMOLECULAR LIPIDS OF THE HYDROCARBON
  154653. RICH MICROALGA BOTRYOCOCCUS BRAUNII. CHEMICAL STRUCTURE AND BIOSYNTHESIS. GEOCHEMICAL AND BIOTECHNOLOGICAL IMPORTANCE. PROG IN THE CHEM OF ORG NAT PROD 199L, 57, 1
  154654. 70.  A REVIEW
  154655. GABRIEL WEATHERHEAD
  154656. 7735N
  154657. 2/28/96V
  154658. LEWIS, J. R. MUSCARINE, OXAZOLE, THIAZOLE, IMIDAZOLE AND PEPTIDE ALKALOIDS AND OTHER MISCELLANEOUS ALKALOIDS. NAT PROD RPTS 1992, 9(1), 81
  154659. 101.  A REVIEWa
  154660. GABRIEL WEATHERHEAD
  154661. 7736N
  154662. 2/28/96VcTURNER, A. B. STEROIDS: REACTIONS AND PARTIAL SYNTHESES. NAT PROD RPTS I992, 9(1), 37
  154663. 79.  A REVIEWa
  154664. GABRIEL WEATHERHEAD
  154665. 7737N
  154666. 2/28/96
  154667. VmMICHAEL, J. P. QUINOLINE, QUINAZOLINE, AND ACRIDONE ALKALOIDS. NATURAL PROD RPTS 1992, 9(1), 25
  154668. 35.  A REVIEWa
  154669. GABRIEL WEATHERHEAD
  154670. 7738N
  154671. 2/28/96VuPINDER, A. R. PYRROLE, PYRROLIDINE, PIPERIDINE, AND AZEPINE ALKALOIDS. NATURAL PROD RPTS 1992, 9(1), 17
  154672. 23.  A REVIEWa
  154673. GABRIEL WEATHERHEAD
  154674. 7739N
  154675. 2/28/96VHHANSON, J. R. DITERPENOIDS. NATURAL PROD RPTS 1992, 9(1),1
  154676. 16.  A REVIEWa
  154677. GABRIEL WEATHERHEAD
  154678. 7740N
  154679. 2/28/96V_FODOR, G.; DHARANIPRAGADA, R. TROPANE ALKALOIDS. NATURAL PROD RPTS 1991, 8(6),603
  154680. 12.  A REVIEWa
  154681. GABRIEL WEATHERHEAD
  154682. 7741N
  154683. 2/28/96V`SIMPSON, T. J. THE BIOSYNTHESIS OF POLYKETIDES. NATURAL PROD RPTS 1991 8(6),573 FF O2.  A REVIEWa
  154684. GABRIEL WEATHERHEAD
  154685. 7742N
  154686. 2/28/96VfMICHAEL, J. P. INDOLIZIDINE AND QUINOLIZIDINE ALKALOIDS. NATURAL PROD RPTS 1991,8(6),553
  154687. 72.  A REVIEWa
  154688. GABRIEL WEATHERHEAD
  154689. 7743N
  154690. 2/28/96
  154691. AKHTAR, M.; WRIGHT, J. N. A UNIFIED MECHANISTIC VIEW OF OXIDATIVE REACTIONS CATALYZED BY P
  154692. 450 AND RELATED IRONCONTAINING ENZYMES. NATURAL PROD RPTS 1991, 8(6), 527
  154693. 51.  A REVIEWa
  154694. GABRIEL WEATHERHEAD
  154695. 7744N
  154696. 2/28/96V
  154697. RUASSE, MARIE
  154698. FRANCOISE; MOTALLEBI, SHAHROKH. SOLVATION, THE ELECTROPHILIC DRIVING FORCE OF IONIC BROMINATION OF ETHYLENIC COMPOUNDS. THE ADDITION
  154699. SOLVOLYSIS ANALOGY. J PHYS ORG CHEM 1991,4,527
  154700. 535.  A REVIEWa
  154701. GABRIEL WEATHERHEAD
  154702. 7745N
  154703. 2/28/96V
  154704. DIAS, JERRY RAY. THE CURRENT STATUS OF ISOMER ENUMERATION OF USEFUL BENZENOIDS AND A NEW TOPOLOGICAL PARADIGM. J PHYS ORG CHEM 1990, 3, 765
  154705. 783.  A REVIEWa
  154706. GABRIEL WEATHERHEAD
  154707. 7746N
  154708. 2/28/96VrSLIWA, WANDA; BACHOWSKA, BARBARA; ZELICHOWICZ, NATALIA. CHEMISTRY OF VIOLOGENS. 1991, 32(11), 2241
  154709. 2273.  A REVIEWa
  154710. GABRIEL WEATHERHEAD
  154711. 7747N
  154712. 2/28/96
  154713. BOX, VERNON G. S. THE RELATIONSHIP BETWEEN BOND TYPE BOND ORDER AND BOND LENGTH. A RE
  154714. EVALUATION OF THE AROMATICITY OF SOME HETEROCYCLIC MOLECULES. HETEROCYCLES1991, 32(10), 2023
  154715. 2041.  A REVIEWa
  154716. GABRIEL WEATHERHEAD
  154717. 7748N
  154718. 2/28/96V
  154719. COLONNA, MARTINO; POLONI, MARINO. THE ROLE OF THE ALPHA
  154720. EFFECT IN THERMOLYSIS, PHOTOLYSIS AND ELECTRON
  154721. TRANSFER PROCESSES. GAZZETTA CHIMICA ITALIANA 1991,121(10), 461
  154722. 70.  A REVIEWa
  154723. GABRIEL WEATHERHEAD
  154724. 7749N
  154725. 2/28/96V
  154726. MAYR, HERBERT; BARAN, JANUSZ; HEIGL, ULRICH W. 3,3,4,4,5,5
  154727. HEXAMETHYL1,2
  154728. BIS(METHYLENE)CYCLOPENTANE: A NOVEL PROBE FOR THE STUDY OF CYCLOADDITION MECHANISMS. GAZZETTA CHIMICA ITALIANA 1991, 121(8), 373
  154729. 81.  A REVIEWa
  154730. GABRIEL WEATHERHEAD
  154731. 7750N
  154732. 2/28/96V
  154733. BRANDI, ALBERTO; CICCHI, STEFANO; GOTI, ANDREA; PIETRUSIEWICZ, K. MICHAL. REGIO
  154734.  AND STEREOSELECTIVE SYNTHESIS OF ISOXAZOLIDINES BEARING PHOSPHINYL SUBSTITUENTS. GAZZETTA CHIMICA ITALIANA 1991, 121(6), 285
  154735. 95.  A REVIEW
  154736. GABRIEL WEATHERHEAD
  154737. 7751N
  154738. 2/28/96V
  154739. WALDMANN, HERBERT; BRAUN, MATTHIAS. AMINO ACID ESTERS AS CHIRAL AUXILIARIES IN ASYMMETRIC CYCLOADDITIONS. GAZZETTA CHIMICA ITALIANA 1991, 121(6), 277
  154740. 84.  A REVIEWa
  154741. GABRIEL WEATHERHEAD
  154742. 7752N
  154743. 2/28/96V
  154744. YOUNES, MANSOUR ISMAIL; ATTA, ALY HUSSEIN; METWALLY, SAOUD A. M.; ELNAGDI, MOHAMED HILMY. SYNTHESIS OF PYRANOPYRAZOLES. GAZZETTA CHIMICA ITALIANA 1991,121(4), 185
  154745. 95.  A REVIEWa
  154746. GABRIEL WEATHERHEAD
  154747. 7753N
  154748. 2/28/96VvKUCZKOWSKI, ROBERT L. THE STRUCTURE AND MECHANISM OF FORMATION OF OZONIDES. CHEM SOC REV 1992, 21(1), 79
  154749. 83.  A REVIEWa
  154750. GABRIEL WEATHERHEAD
  154751. 7754N
  154752. 2/28/96VzGOKEL, GEORGE W. LARIAT ETHERS: FROM SIMPLE SIDEARMS TO SUPRAMOLECULAR SYSTEMS. CHEM SOC REV 1992, 21(1), 39
  154753. 47.  A REVIEWa
  154754. GABRIEL WEATHERHEAD
  154755. 7755N
  154756. 2/28/96
  154757. VzGREEN, MALCOLM L. H.
  154758.  MOUNTFORD, PHILIP. CYCLOPENTADIENYL MOLYBDENUM AND TUNGSTEN DIHALIDES. 1992, 21(1), 29
  154759. 38.  A REVIEWa
  154760. GABRIEL WEATHERHEAD
  154761. 7756N
  154762. 2/28/96
  154763. RUDLER, H.; AUDOUIN, M.; CHELAIN, E.; DENISE, B.; GOUMONT, R. AMINOCARBENE COMPLEXES OF CHROMIUM AND MOLYBDENUM: INITIATORS FOR CASCADE REACTIONS WITH ALKYNES LEADING TO NEW HETEROCYCLIC COMPOUNDS VIA NITROGEN YLIDES. CHEM SOC REV 1991, 20(4), 503
  154764. 31.  A REVIEW
  154765. GABRIEL WEATHERHEAD
  154766. 7757N
  154767. 2/28/96V
  154768. LEITES, L. A. VIBRATIONAL SPECTROSCOPY OF CARBORANES AND PARENT BORANES AND ITS CAPABILITIES IN CARBORANE CHEMISTRY. CHEM REV 1992, 92(2), 279
  154769. 323.  A REVIEWa
  154770. GABRIEL WEATHERHEAD
  154771. 7758N
  154772. 2/28/96VoPLESEK, JAROMIR. POTENTIAL APPLICATIONS OF THE BORON CLUSTER COMPOUNDS. CHEM REV 1992, 92(2), 269
  154773. 78.  A REVIEWa
  154774. GABRIEL WEATHERHEAD
  154775. 7759N
  154776. 2/28/96
  154777. VqGRIMES, RUSSELL N. BORON
  154778. CARBON RING LIGANDS IN ORGANOMETALLIC SYNTHESIS. CHEM REV 1992, 92(2), 251
  154779. 68.  A REVIEWa
  154780. GABRIEL WEATHERHEAD
  154781. 7760N
  154782. 2/28/96VMSTIBR, BOHUMIL. CARBORANES OTHER THAN C2BIOHL2. 1992, 92(2) 225
  154783. 50.  A REVIEWa
  154784. GABRIEL WEATHERHEAD
  154785. 7761N
  154786. 2/28/96VsBREGADZE, V. I. DICARBA
  154787. CLOSO
  154788. DODECABORANES C2BIOHI2 AND THEIR DERIVATIVES. CHEM REV 1992, 92(2), 209
  154789. 23.  A REVIEWa
  154790. GABRIEL WEATHERHEAD
  154791. 7762N
  154792. 2/28/96V
  154793. WILLIAMS, ROBERT E. THE POLYBORANE, CARBORANE, CARBOCATION CONTINUUM: ARCHITECTURAL PATTERNS. CHEM REV 1992, 92(2), 177
  154794. 207.  A REVIEWa
  154795. GABRIEL WEATHERHEAD
  154796. 7763N
  154797. 2/28/96VfMUZART, J. CHROMIUM
  154798. CATALYZED OXIDATIONS IN ORGANIC SYNTHESIS. CHEM REV 1992, 92(1), 113
  154799. 40.  A REVIEWa
  154800. GABRIEL WEATHERHEAD
  154801. 7764N
  154802. 2/28/96
  154803. WELKER, MARK E. 3 + 2 CYCLOADDITION REACTIONS OF TRANSITION
  154804. METAL 2
  154805. ALKYNYL AND 
  154806. ALLYL COMPLEXES AND THEIR UTILIZATION IN FIVE
  154807. MEMBERED
  154808. RING COMPOUND SYNTHESES. CHEM REV 1992, 92(1), 97
  154809. 112.  A REVIEWa
  154810. GABRIEL WEATHERHEAD
  154811. 7765N
  154812. 2/28/96V
  154813. OLAH, GEORGE A.; REDDY, V. PRAKASH; PRAKASH, G. K. SURYA LONG
  154814. LIVED CYCLOPROPYLCARBINYL CATIONS. CHEM REV 1992, 92(1), 69
  154815. 95.  A REVIEWa
  154816. GABRIEL WEATHERHEAD
  154817. 7766N
  154818. 2/28/96VqMOLANDER, GARY A. APPLICATION OF LANTHANIDE REAGENTS IN ORGANIC SYNTHESIS. CHEM REV 1992, 92(1), 29
  154819. 68.  A REVIEWa
  154820. GABRIEL WEATHERHEAD
  154821. 7767N
  154822. 2/28/96V
  154823. ROUNDHILL, D. MAX. TRANSITION METAL AND ENZYME CATALYZED REACTIONS INVOLVING REACTIONS WITH AMMONIA AND AMINES. CHEM REV 1992, 92(1), 1
  154824. 27.  A REVIEWa
  154825. GABRIEL WEATHERHEAD
  154826. 7768N
  154827. 2/28/96
  154828. CAMBIE, RICHARD C.; RUTLEDGE, PETER S.; WOODGATE, PAUL D. SYNTHETIC ANTHRACYCLINES FROM ANTHRAQUINONES. AUSTRALIAN JOC 1992, 45(3), 483
  154829. 512.  A REVIEWa
  154830. GABRIEL WEATHERHEAD
  154831. 7769N
  154832. 2/28/96V
  154833. PINHEY, JOHN T. ORGANOLEAD(IV) TRICARBOXYLATES, NEW REAGENTS FOR ORGANIC SYNTHESIS. AUSTRALIAN JOC1991, 44(10),1353
  154834. 82.  A REVIEWa
  154835. GABRIEL WEATHERHEAD
  154836. 7770N
  154837. 2/28/96VsCLEZY, PETER S. STUDIES IN PORPHYRIN CHEMISTRY: A SYNTHETIC APPROACH. 1991, AUSTRALIAN JOC 44(9),1163
  154838. 93.  A REVIEWa
  154839. GABRIEL WEATHERHEAD
  154840. 7771N
  154841. 2/28/96VSBANWELL, MARTIN G. NEW METHODS FOR THE SYNTHESIS OF TROPONOID COMPOUNDS.   A REVIEWa
  154842. GABRIEL WEATHERHEAD
  154843. 7772N
  154844. 2/28/96V}BRUCE, MICHAEL I.; WHITE, ALLAN H. SOME CHEMISTRY OF PENTAKIS(METHOXYCARBONYL)CYCLOPENTADIENE. 1990, 43(6), 949
  154845. 95.  A REVIEWa
  154846. GABRIEL WEATHERHEAD
  154847. 7773N
  154848. 2/28/96
  154849. GLEITER, ROLF. CYCLOALKADIYNES
  154850. FROM BENT TRIPLE BONDS TO STRAINED CAGE COMPOUNDS. ANGEW CHEM, INT ED ENG 1992, 31(1), 27
  154851. 44.  A REVIEWa
  154852. GABRIEL WEATHERHEAD
  154853. 7774N
  154854. 2/28/96V
  154855. LOCKHOFF, OSWALD. GLYCOLIPIDS AS IMMUNOMODULATORS
  154856.  SYNTHESIS AND PROPERTIES. ANGEW CHEM, INT ED ENG 1991, 30(12),1611
  154857. 20.  A REVIEWa
  154858. GABRIEL WEATHERHEAD
  154859. 7775N
  154860. 2/28/96V
  154861. GOLDMANN, SIEGFRIED; STOLTEFUSS, JURGEN. 1,4
  154862. DIHYDROPYRIDINES: EFFECT OF CHIRALITY AND CONFORMATION ON THE CALCIUM ANTAGONISTIC AND CALCIUM AGONISTIC ACTIVITIES. ANGEW CHEM, INT ED ENG 1991, 30(12), 1559
  154863. 78.  A REVIEWa
  154864. GABRIEL WEATHERHEAD
  154865. 7776N
  154866. 2/28/96V
  154867. REETZ, MANFRED T. NEW APPROACHES TO THE USE OF AMINO ACIDS AS CHIRAL BUILDING BLOCKS IN ORGANIC SYNTHESIS. ANGEW CHEM, INT ED ENG 1991, 30(12), 1531
  154868. 46.  A REVIEWa
  154869. GABRIEL WEATHERHEAD
  154870. 7777N
  154871. 2/28/96
  154872. VrMULZER, JOHANN. ERYTHROMYCIN SYNTHESIS
  154873. A NEVER ENDING STORY? ANGEW CHEM, INT ED ENG 1991, 30(11),1452
  154874. 4.  A REVIEWa
  154875. GABRIEL WEATHERHEAD
  154876. 7778N
  154877. 2/28/96V
  154878. SCHELLENBERGER, VOLKER; JAKUBKE, HANS DIETER. PROTEASE
  154879. CATALYZED KINETICALLY CONTROLLED PEPTIDE SYNTHESIS. ANGEW CHEM, INT ED ENG 1991, 30(11), 1437
  154880. 49.  A REVIEWa
  154881. GABRIEL WEATHERHEAD
  154882. 7779N
  154883. 2/28/96V
  154884. SCHNEIDER, HANS
  154885. JORG. MECHANISMS OF MOLECULAR RECOGNITION: INVESTIGATION OF ORGANIC HOST
  154886. GUEST COMPLEXES. ANGEW CHEM, INT ED ENG 1991, 30(11), 1417
  154887. 36.  A REVIEWa
  154888. GABRIEL WEATHERHEAD
  154889. 7780N
  154890. 2/28/96V
  154891. NICOLAOU, K. C.; DAI, W.
  154892. M. CHEMISTRY AND BIOLOGY OF ENEDIYNE ANTICANCER ANTIBIOTICS. ANGEW CHEM, INT ED ENG 1991, 30(11),1387
  154893. 1416.  A REVIEWa
  154894. GABRIEL WEATHERHEAD
  154895. 7781N
  154896. 2/28/96V
  154897. CONSTABLE, EDWIN C. HELICES, SUPRAMOLECULAR CHEMISTRY AND METAL
  154898. DIRECTED SELF ASSEMBLY. ANGEW CHEM, INT ED ENG 1991, 30(11), 1450
  154899. 1.  A REVIEWa
  154900. GABRIEL WEATHERHEAD
  154901. 7782N
  154902. 2/28/96VmWALDMANN, HERBERT. LICIO4 IN ETHER
  154903. AN UNUSUAL SOLVENT. ANGEW CHEM, INT ED ENG 1991, 30(10), 1306
  154904. 8.  A REVIEWa
  154905. GABRIEL WEATHERHEAD
  154906. 7783N
  154907. 2/28/96V
  154908. TASHMA, RACHEL; RAPPOPORT, ZVI. SOLVENT
  154909. INDUCED CHANGES IN THE SELECTIVITY OF SOLVOLYSES IN AQUEOUS ALCOHOLS AND RELATED MISTURES. ADV PHYS ORG CHEM 1992, 27, 239
  154910. 291.  A REVIEWa
  154911. GABRIEL WEATHERHEAD
  154912. 7784N
  154913. 2/28/96VqBERNASCONI, CLAUDE F. THE PRINCIPLE OF NON
  154914. PERFECT SYNCHRONIZATION. ADV PHYS ORG CHEM1992, 27, 119
  154915. 238.  A REVIEWa
  154916. GABRIEL WEATHERHEAD
  154917. 7785N
  154918. 2/28/96V
  154919. LEE, CHOON. CROSS
  154920. INTERACTION CONSTANTS AND TRANSITIONSTATE STRUCTURE IN SOLUTION. ADV PHYS ORG CHEM 1992, 27, 57
  154921. 117.  A REVIEWa
  154922. GABRIEL WEATHERHEAD
  154923. 7786N
  154924. 2/28/96V|WILLIAMS, ANDREW. EFFECTIVE CHARGE AND TRANSITION
  154925. STATE STRUCTURE IN SOLUTION. ADV IN PHY ORG CHEM 1992, 27,1
  154926. 55.   A REVIEWa
  154927. GABRIEL WEATHERHEAD
  154928. 7787N
  154929. 2/28/96
  154930. JANIAK, CHRISTOPH; SCHUMANN, HERBERT. BULKY OR SUPRACYCLOPENTADIENYL DERIVATIVES IN ORGANOMETALLIC CHEMISTRY. ADV IN ORGANOMETALLIC CHEM 1991, 33, 291
  154931. 393.     A REVIEWa
  154932. GABRIEL WEATHERHEAD
  154933. 7788N
  154934. 2/28/96V
  154935. FRIEDRICH, HOLGER B.; MOSS, JOHN R. HALOGENOALKYL COMPLEXES OF TRANSITION METALS. ADV IN ORGANOMETALLIC CHEM 1991, 33, 235
  154936. 290.  A REVIEWa
  154937. GABRIEL WEATHERHEAD
  154938. 7789N
  154939. 2/28/96VaMOLLOY, KIERAN C. ORGANOTIN HETEROCYCLES. ADV IN ORGANOMETALLIC CHEM 1991, 33, 171
  154940. 234.  A REVIEWa
  154941. GABRIEL WEATHERHEAD
  154942. 7790N
  154943. 2/28/96V
  154944. GREV, ROGER S. STRUCTURE AND BONDING IN THE PARENT HYDRIDES AND MULTIPLY BONDED SILICON AND GERMANIUM COMPOUNDS: FROM MHN TO R2M=M'R2 AND RM=M'R. ADV IN ORGANOMETALLIC CHEM 1991, 33, 125
  154945. 170.  A REVIEWa
  154946. GABRIEL WEATHERHEAD
  154947. 7791N
  154948. 2/28/96V}KOCHI, JAY K.; BOCKMAN, T. MICHAEL. ORGANOMETALLIC IONS AND ION PAIRS. ADV IN ORGANOMETALLIC CHEM 1991, 33, 52
  154949. 124.  A REVIEWa
  154950. GABRIEL WEATHERHEAD
  154951. 7792N
  154952. 2/28/96V
  154953. JORDAN, RICHARD F. CHEMISTRY OF CATIONIC DICYCLO PENTADIENYL GROUP 4 METAL
  154954. ALKYL COMPLEXES. ADV IN ORGANOMETALLIC CHEM 1991, 32, 325
  154955. 387.  A REVIEWa
  154956. GABRIEL WEATHERHEAD
  154957. 7793N
  154958. 2/28/96V
  154959. MAYR, ANDREAS; HOFFMAIESTER, HANS. RECENT ADVANCES IN THE CHEMISTRY OF METAL
  154960. CARBON TRIPLE BONDS. ADV IN ORGANOMETALLIC CHEM 1991, 32, 227
  154961. 324.  A REVIEWa
  154962. GABRIEL WEATHERHEAD
  154963. 7794N
  154964. 2/28/96V
  154965. MARKIES, PETER R.; AKKERMAN, OTTO S.; BICKELHAUPT, FRIEDRICH; SMEETS, WILBERTH J. J.; SPEK, ANTHONY L. X
  154966. RAY STRUCTURAL ANALYSES OF ORGANOMAGNESIUM COMPOUNDS. ADV IN ORGANOMETALLIC CHEM 1991, 32, 147
  154967. 226.  A REVIEWa
  154968. GABRIEL WEATHERHEAD
  154969. 7795N
  154970. 2/28/96V
  154971. KALCK, PHILIPPE; PERES, YOLANDE; JENCK, JEAN. HYDROFORMYLATION CATALYZED BY RUTHENIUM COMPLEXES. ADV IN ORGANOMETALLIC CHEM 1991, 32, 121
  154972. 146.  A REVIEWa
  154973. GABRIEL WEATHERHEAD
  154974. 7796N
  154975. 2/28/96
  154976. LINFORD, LORNA; RAUBENHEIMER HELGARD G. FORMATION AND REACTIONS OF ORGANOSULFUR AND ORGANOSELENIUM ORGANOMETALLIC COMPOUNDS. ADV IN ORGANOMETALLIC CHEM 1991, 32,1
  154977. 120.  A REVIEWa
  154978. GABRIEL WEATHERHEAD
  154979. 7797N
  154980. 2/28/96V
  154981. GARG, HARI; LYON, NANCY. STRUCTURE OF COLLAGEN FIBRIL ASSOCIATED, SMALL PROTEOGLYCANS OF MAMMALIAN ORIGIN. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 239
  154982. 261.     A REVIEWa
  154983. GABRIEL WEATHERHEAD
  154984. 7798N
  154985. 2/28/96V
  154986. DAVID, SERGE; AUGE, CLAUDINE; GAUTHERON, CHRISTINE. ENZYMIC METHODS IN PREPARATIVE CARBOHYDRATE CHEMISTRY. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 176
  154987. 237.  A REVIEWa
  154988. GABRIEL WEATHERHEAD
  154989. 7799N
  154990. 2/28/96V|STOSS, PETER; HEMMER, REINHARD. 1,4:3,6
  154991. DIANHYDRO HEXITOLS. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 93
  154992. 173.  A REVIEWa
  154993. GABRIEL WEATHERHEAD
  154994. 7800N
  154995. 2/28/96
  154996. SOMSAK, LASZLO; FERRIER, ROBERT J. RADICAL
  154997. MEDIATED BROMINATIONS AT RING POSITIONS OF CARBOHYDRATES. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 37
  154998. 92.  A REVIEWa
  154999. GABRIEL WEATHERHEAD
  155000. 7801N
  155001. 2/28/96V
  155002. ANGYAL, STEPHEN J. THE COMPOSITION OF REDUCING SUGARS IN SOLUTION: CURRENT ASPECTS. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49,19
  155003. 36.   A REVIEWa
  155004. GABRIEL WEATHERHEAD
  155005. 7802N
  155006. 2/28/96VuPERCHERON, FRANCOIS. COURTOIS, JEAN EMILE, 1907
  155007. 1989. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 11
  155008. 18.  A REVIEWa
  155009. GABRIEL WEATHERHEAD
  155010. 7803N
  155011. 2/28/96V
  155012. LIPTAK, ANDRAS; NANASI, PAL; SZTARICSKAI, FERENC. BOGNAR, REZNO, 1913
  155013. 1990. ADV IN CARBOHYDRATE CHEM AND BIOCHEM 1991, 49, 3
  155014. 10.  A REVIEWa
  155015. GABRIEL WEATHERHEAD
  155016. 7804N
  155017. 2/28/96V
  155018. CHATGILIALOGLU, CHRYSSOSTOMOS. ORGANOSILANES AS RADICAL
  155019. BASED REDUCING AGENTS IN SYNTHESIS. ACC CHEM RES 1992, 25(4),188
  155020. 94.     A REVIEWa
  155021. GABRIEL WEATHERHEAD
  155022. 7805N
  155023. 2/28/96VmHUANG, YAOZENG. SYNTHETIC APPLICATIONS OF ORGANOANTIMONY COMPOUNDS. ACC CHEM RES 1992, 25(4),182
  155024. 7.  A REVIEWa
  155025. GABRIEL WEATHERHEAD
  155026. 7806N
  155027. 2/28/96V
  155028. WUDL, FRED. THE CHEMICAL PROPERTIES OF BUCKMINSTERFULLERENE (C60) AND THE BIRTH AND INFANCY OF FULLEROIDS. ACC CHEM RES 1992, 25(3), 157
  155029. 61.  A REVIEWa
  155030. GABRIEL WEATHERHEAD
  155031. 7807N
  155032. 2/28/96V
  155033. FAGAN, PAUL J.; CALABRESE, JOSEPH C.; MALONE, BRIAN. METAL COMPLEXES OF BUCKMINSTERFULLERENE (C60). ACC CHEM RES 1992, 25(3), 134
  155034. 42.  A REVIEWa
  155035. GABRIEL WEATHERHEAD
  155036. 7808N
  155037. 2/28/96V
  155038. MATHEY, FRANCOIS. EXPANDING THE ANALOGY BETWEEN PHOSPHORUS
  155039. CARBON AND CARBON CARBON DOUBLE BONDS. ACC CHEM RES 1992, 25(2), 90
  155040. 6.  A REVIEWa
  155041. GABRIEL WEATHERHEAD
  155042. 7809N
  155043. 2/28/96
  155044. CANTY, ALLAN J. DEVELOPMENT OF ORGANOPALLADIUM(IV) CHEMISTRY: FUNDAMENTAL ASPECTS AND SYSTEMS FOR STUDIES OF MECHANISM IN ORGANOMETALLIC CHEMISTRY AND CATALYSIS. ACC CHEM RES 1992, 25(2), 83
  155045. 90.  A REVIEWa
  155046. GABRIEL WEATHERHEAD
  155047. 7810N
  155048. 2/28/96V
  155049. MARKS, TOBIN J. SURFACE
  155050. BOUND METAL HYDROCARBYLS. ORGANOMETALLIC CONNECTIONS BETWEEN HETEROGENEOUS AND HOMOGENEOUS CATALYSIS. ACC CHEM RES 1992, 25(2), 57
  155051. 65.  A REVIEWa
  155052. GABRIEL WEATHERHEAD
  155053. 7811N
  155054. 2/28/96V
  155055. MCMURRY, JOHN E.; LECTKA, THOMAS. THREE
  155056. CENTER, TWO
  155057. ELECTRON C
  155058. C BONDS IN ORGANIC CHEMISTRY. ACC CHEM RES 1992, 25(1), 47
  155059. 53.  A REVIEWa
  155060. GABRIEL WEATHERHEAD
  155061. 7812N
  155062. 2/28/96V
  155063. KOCHI, JAY K. INNER
  155064. SPHERE ELECTRON TRANSFER IN ORGANIC CHEMISTRY. RELEVANCE TO ELECTROPHILIC AROMATIC NITRATION. ACC CHEM RES 1992, 25(1), 39
  155065. 47.  A REVIEWa
  155066. GABRIEL WEATHERHEAD
  155067. 7813N
  155068. 2/28/96
  155069. CREARY, XAVIER. REACTIONS OF HALODIAZIRINES BY SN2' AND ELECTRON TRANSFER INITIATED PROCESSES. ACC CHEM RES 1992, 25(1), 31
  155070. 8.  A REVIEWa
  155071. GABRIEL WEATHERHEAD
  155072. 7814N
  155073. 2/28/96V
  155074. BROWN, HERBERT C.; RAMACHANDRAN, P. VEERARAGHAVAN. ASYMMETRIC REDUCTION WITH CHIRAL ORGANOBORANES BASED ON ALPHA
  155075. PINENE. ACC CHEM RES 1992, 25(1), 16
  155076. 24.  A REVIEWa
  155077. GABRIEL WEATHERHEAD
  155078. 7815N
  155079. 2/28/96V
  155080. BERNASCONI, CLAUDE F. THE PRINCIPLE OF NONPERFECT SYNCHRONIZATION: MORE THAN A QUALITATIVE CONCEPT? ACC CHEM RES 1992, 25(1),9
  155081. 16.  A REVIEWa
  155082. GABRIEL WEATHERHEAD
  155083. 7816N
  155084. 2/28/96VvBUNNETT, JOSEPH F. RADICAL
  155085. CHAIN, ELECTRON
  155086. TRANSFER DEHALOGENATION REACTIONS. ACC CHEM RES 1992, 25(1), 2
  155087. 9.  A REVIEWa
  155088. GABRIEL WEATHERHEAD
  155089. SYNLETTCoPANDEY REVIEW AMINE PHOTOCHEM ELECTRON TRANSFER IMINIUM AZOMETHINE YLIDE DIPOLE DESILYLATION CYCLIZATION REVIEWM
  155090. 7817N
  155091. 2/28/96
  155092. VXSYNTHETIC PERSPECTIVES OF PHOTOINDUCED ELECTRON TRANSFER GENERATED AMINE RADICAL CATIONSW
  155093. 1992 P 546a
  155094. GABRIEL WEATHERHEAD
  155095. SYNLETTCbITO NICKEL CATALYST CYCLIZATION INTRAMOLECULAR ENYNE ISONITRILE INSERTION REVIEW MECHANISM SILICONM
  155096. 7818N
  155097. 2/28/96VXNICKEL (O) MEDIATED INTRAMOLECULAR CYCLIZATIONS OF ENEYNE, DIENES, BIS
  155098. DIENES AND DIYNESW
  155099. 1992 P 539a
  155100. GABRIEL WEATHERHEAD
  155101. SYNLETTCPSATOH HALO SULFOXIDE REVIEW SYNTHESIS CARBANION EPOXIDE REARRANGEMENT STEREOCHEMM
  155102. 7819N
  155103. 2/28/96VBRECENT DEVELOPMENTS IN ORGANIC SYNTHESIS WITH HALO ARYL SULFOXIDESW
  155104. 1992 P 455a
  155105. GABRIEL WEATHERHEAD
  155106. CHEM TRACTCbMARSHALL REVIEW TIN STANNANE LEWIS ACID ALLYL ADDITION CARBONYL STEREOCHEM CHIRAL ENANTIOSELECTIVEM
  155107. 7820N
  155108. 2/28/96VlCHIRAL ALKOXYALLYLIC AND ALLENIC STANNANES AS REAGENTS FOR DIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESISW    1992 P 75a
  155109. GABRIEL WEATHERHEAD
  155110. ORG PREP PROCEDURE INT
  155111. RING CLOSURE REACTIONS MANY MEMBERED RINGS ALKALI METAL BIFUNCTIONAL CHAINS DIMETHYL SULFOXIDE FREE ENERGIES REACTIVITY MOLECULES ETHERS SALTS GALLI CM
  155112. 7821N
  155113. 2/28/96V='CESIUM ION EFFECT' AND MACROCYCLIZATION   A CRITICAL REVIEW.W
  155114. 1992 JUNX
  155115. 24(3)a
  155116. GABRIEL WEATHERHEAD
  155117. ORG PREP PROCEDURE INTC
  155118. FRIEDEL CRAFTS CYCLIALKYLATIONS ORGANIC SYNTHESIS STEREOSELECTIVE CYCLIZATION PEA SEEDLINGS ACID ALLYLSILANES CYCLASE 2,3 OXIDOSQUALENE MECHANISM (+/ ) APHIDICOLIN TAYLOR SKM
  155119. 7822N
  155120. 2/28/96VDBIOSYNTHETIC, BIOMIMETIC AND RELATED EPOXIDE CYCLIZATIONS  A REVIEW.W
  155121. 1992 JUNX
  155122. 24(3)a
  155123. GABRIEL WEATHERHEAD
  155124. SYNLETTCrACHIWA REVIEW CHIRAL ASYMMETRIC HYDROGENATION REDUCTION LIGAND PHOSPHINE PHOSPHOROUS RHODIUM WILKINSON BIPHOSPHINEM
  155125. 7823N
  155126. 2/28/96V}DESIGN CONCEPTS FOR DEVELOPING HIGHLY EFFICIENT CHIRAL BISPHOSPHINE LIGANDS IN THE RHODIUM CATALYZED ASYMMETRIC HYDROGENATIONW
  155127. 1992 P 169a
  155128. GABRIEL WEATHERHEAD
  155129. Tet. Lett.
  155130. CaMOLINA INTRAMOLECULAR AZIDE DIPOLAR CYCLOADDITION EPOXIDE STAUDINGER AZIRIDINE REVIEW PHOSPHOROUSM
  155131. 7824N
  155132. 2/28/96VaA REGIOSELECTIVE ENTRY TO AZIRINO INDOLE BY EPOXIDATION STAUDINGER REACTION OF ALLYLPHENYL AZIDESW
  155133. 1992 P 2387a
  155134. GABRIEL WEATHERHEAD
  155135. ACCOUNTS CHEM RESClBEAK TRANSITION STATE THEORY MECHANISM REVIEW SN2 DISPLACEMENT GEOMETRY INTRAMOLECULAR ENDO RESTRICTION TESTM
  155136. 7825N
  155137. 2/28/96VwDETERMINATION OF TRANSITION STATE GEOMETRIES BY ENDO RESTRICTION TEST MECHANISM OF SUBSTITUTION AT NONSTEREOGENIC ATOMSW
  155138. VOL 25 1992 P 215a
  155139. GABRIEL WEATHERHEAD
  155140. REV HETEROATOM CHEMCQNEGISHI ZIRCONIUM ZIRCOCENE COMPLEX CYCLIZATION HETEROCYCLE ORGANOMETALLIC REVIEWM
  155141. 7826N
  155142. 2/28/96VEZIRCOCENE ALKENE COMPLEXES.  THEIR FORMATION, STRUCTURE AND REACTIONSW
  155143. VOL 6 1992 P 177a
  155144. GABRIEL WEATHERHEAD
  155145. REV HETEROATOM CHEMC]PADWA VINYL SULFONE ALLENE REVIEW CYCLIZATION CYCLOADDITION DIELS ALDER DIPOLAR CYCLOADDITIONM
  155146. 7827N
  155147. 2/28/96
  155148. VTCYCLOADDITION AND CYCLIZATION REACTIONS OF UNSATURATED SULFONES IN ORGANIC SYNTHESISW
  155149. VOL 6 1992 P 241a
  155150. GABRIEL WEATHERHEAD
  155151. REV HETEROATOM CHEMCkSATOH REVIEW EPOXIDE SULFONE SULFONYL SULFOXIDE OXIRANE REARRANGEMENT CARBANION RING OPENING INTRAMOLECULARM
  155152. 7828N
  155153. 2/28/96V>ORGANIC SYNTHESIS WITH SULFINYL OXIRANES AND SULFONYL OXIRANESW
  155154. VOL 6 1992 P 218a
  155155. GABRIEL WEATHERHEAD
  155156. REV HETEROATOM CHEMCJARAI CHIRAL SULFOXIDE REVIEW LIGAND ALLENE DIELS ALDER DIASTEROSELECTIVITYM
  155157. 7829N
  155158. 2/28/96V
  155159. SYNTHESIS AND ASYMMETRIC DIELS ALDER REACTIONS OF CHIRAL UNSATURATED SULFOXIDES BEARING A BORNYL GROUP AS AN EFFICIENT LIGAND ON THE SULFUR CENTERW
  155160. VOL 6 1992 P 202a
  155161. GABRIEL WEATHERHEAD
  155162. ORG PREP PROCEDURE INT
  155163. IMINOPHOSPHORANE MEDIATED SYNTHESIS ELECTROCYCLIC RING CLOSURE ONE POT SYNTHESIS N VINYLIC LAMBDA 5 PHOSPHAZENES TRIVALENT PHOSPHORUS COMPOUNDS STAUDINGER REACTION DIETHYL AZODICARBOXYLATE CONJUGATED CARBODIIMIDES ISOQUINOLINE DERIVATIVES QUINAZOLINE DERIVATIVES EGUCHI S
  155164. 7830N
  155165. 2/28/96V=THE AZA WITTIG REACTION IN HETEROCYCLIC SYNTHESIS   A REVIEW.W
  155166. 1992 APRX
  155167. 24(2)a
  155168. GABRIEL WEATHERHEAD
  155169. J ORG CHEMCWTOSMIC REAGENT PYRROLE PREPARATION SULFONE HETEROCYCLE REVIEW PHENYLSULFONYL VAN LEUSENM
  155170. 7831N
  155171. 2/28/96VlSYNTHESIS OF 3,4 DISUBSTITUTED PYRROLES BEARING SUBSTITUENTS THAT ARE BOTH ELECTRON WITHDRAWING AND DONATINGW
  155172. VOL 57 1992 P 2245a
  155173. GABRIEL WEATHERHEAD
  155174. SYNLETTCXDIYL DIRADICAL EXTRUSION NITROGEN TRAPPING REVIEW REGIOSELECTIVITY INTRAMOLECULAR LITTLEM
  155175. 7832N
  155176. 2/28/96VOFACTORS AFFECTING REGIOSELECTIVITY IN THE INTRAMOLECULAR DIYL TRAPPING REACTIONW
  155177. 1992 P 107a
  155178. GABRIEL WEATHERHEAD
  155179. SYNLETT
  155180. C;BICYCLIC KETAL ETHER CYCLIC REVIEW ENANTIOSELECTIVE KOTSUKIM
  155181. 7833N
  155182. 2/28/96VkBICYCLIC KETALS.  VERSATILE INTERMEDIATES FOR THE STEREOCONTROLLED CONSTRUCTION OF CYCLIC ETHER DERIVATIVESW    1992 P 97a
  155183. GABRIEL WEATHERHEAD
  155184. 7834N
  155185. 2/28/96V_WILLIAMS, T. I. ROBERT ROBINSON
  155186. CHEMIST EXTRAORDINARY. CLARENDON PRESS: OXFORD, 1990. A REVIEW.a
  155187. GABRIEL WEATHERHEAD
  155188. 7835N
  155189. 2/28/96V
  155190. WIELAND, T.; BODANSZKY, M. THE WORLD OF PEPTIDES. A BRIEF HISTORY OF PEPTIDE CHEMISTRY. SPRINGER VERLAG: HEIDELBERG, FRG, 1991. A REVIEW.a
  155191. GABRIEL WEATHERHEAD
  155192. 7836N
  155193. 2/28/96VqSOKOLOV, VIATCHESLAV I. INTRODUCTION TO THEORETICAL STEREOCHEMISTRY. GORDON AND BREACH: NEW YORK, 1991. A REVIEW.a
  155194. GABRIEL WEATHERHEAD
  155195. 7837N
  155196. 2/28/96V
  155197. SOKOLOV, VIATCHESLAV I. CHIRALITY AND OPTICAL ACTIVITY IN ORGANOMETALLIC COMPOUNDS. GORDON AND BREACH: NEWYORK, 1991. A REVIEW.a
  155198. GABRIEL WEATHERHEAD
  155199. 7838N
  155200. 2/28/96
  155201. "VXSCHOMBURG, G. GAS CHROMATOGRAPHY
  155202. A PRACTICAL COURSE. VCH  WEINHEIM, FRG, 1990. A REVIEW.a
  155203. GABRIEL WEATHERHEAD
  155204. 7839N
  155205. 2/28/96V
  155206. SCHNEIDER, HANS JORG, ED. FRONTIERS IN SUPRAMOLECULAR ORGANIC CHEMISTRY AND PHOTOCHEMISTRY. VCH: WEINHEIM, FRG, 1991. A REVIEW.a
  155207. GABRIEL WEATHERHEAD
  155208. 7840N
  155209. 2/28/96V
  155210. OAE, SHIGERU; DOI, JOYCE T. ORGANIC SULFUR CHEMISTRY. VOL. 1. STRUCTURE AND MECHANISM. CRC PRESS: BOCA RATON, FL, 1991. A REVIEW.a
  155211. GABRIEL WEATHERHEAD
  155212. 7841N
  155213. 2/28/96VXKOPECKY, JAN. ORGANIC PHOTOCHEMISTRY. A VISUAL APPROACH.  VCH: NEW YORK, 1991. A REVIEW.a
  155214. GABRIEL WEATHERHEAD
  155215. 7842N
  155216. 2/28/96V
  155217. JORDAN, ROBERT B. REACTION MECHANISMS OF INORGANIC AND ORGANOMETALLIC SYSTEMS. OXFORD UNIVERSITY PRESS: NEW YORK, 1991. A REVIEW.a
  155218. GABRIEL WEATHERHEAD
  155219. 7843N
  155220. 2/28/96
  155221. IZUTSU, KOSUKE. ACID BASE DISSOCIATION CONSTANTS IN DIPOLAR APROTIC SOLVENTS (IUPAC SERIES). BLACKWELL SCIENTIFIC PUBLICATIONS: OXFORD, U.K., 1990. A REVIEW.a
  155222. GABRIEL WEATHERHEAD
  155223. 7844N
  155224. 2/28/96VeIKAN, RAPHAEL. NATURAL PRODUCTS. A LABORATORY GUIDE, 2ND ED. ACADEMIC: SAN DIEGO, CA, 1991. A REVIEW.a
  155225. GABRIEL WEATHERHEAD
  155226. 7845N
  155227. 2/28/96V
  155228. HAUFE, G.; MANN, G. CHEMISTRY OF ALICYCLIC COMPOUNDS. STRUCTURE AND CHEMICALTRANSFORMATIONS. ELSEVIER: AMSTERDAM, 1989. A REVIEW.a
  155229. GABRIEL WEATHERHEAD
  155230. 7846N
  155231. 2/28/96V
  155232. DELIA, THOMAS J.; WARNER, JOHN C. FUSED PYRIMIDINES, PART 4. MISCELLANEOUS SYSTEMS (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 24, PT. 4). WILEY: NEW YORK, 1992. A REVIEW.a
  155233. GABRIEL WEATHERHEAD
  155234. 7847N
  155235. 2/28/96VaCARLSON, ROLF. DESIGN AND OPTIMIZATION IN ORGANIC SYNTHESIS. ELSEVIER: AMSTERDAM, 1992. A REVIEW.a
  155236. GABRIEL WEATHERHEAD
  155237. 7848N
  155238. 2/28/96
  155239. ,VmBOCHKOV, A. F.; ZAIKOV, G. E.; AFANASIEV, V. A. CARBOHYDRATES. VSP: UTRECHT, THE NETHERLANDS, 1991. A REVIEW.a
  155240. GABRIEL WEATHERHEAD
  155241. 7849N
  155242. 2/28/96V
  155243. MINAMI, TORU; YAMAMOTO, IWAO. CHEMISTRY OF PHOSPHONIUM SALTS CONTAINING RING SYSTEMS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155244. GABRIEL WEATHERHEAD
  155245. 7850N
  155246. 2/28/96
  155247. YAMADA, JUN ICHI; YAMAMOTO, YOSHINORI. DEVELOPMENT OF NEW REACTIVITIES AND SELECTIVITIES VIA STABILIZATION ACTIVATION PROCEDURE OF ANIONIC SPECIES WITH GERMANIUM, TIN AND LEAD.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.
  155248. GABRIEL WEATHERHEAD
  155249. 7851N
  155250. 2/28/96V
  155251. STONE, JOHN A. THE STABILIZATION OF CARBENIUM IONS BY SILICON SUBSTITUENTS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155252. GABRIEL WEATHERHEAD
  155253. 7852N
  155254. 2/28/96
  155255. 2YOSHIDA, JUN ICHI; MURATA, TOSHIKI; MATSUNAGA, SHINICHIRO; MAEKAWA, TSUYOSHI; SHIOZAWA, SATOSHI; ISOE, SACHIHIKO. BETA SILICON EFFECTS IN ELECTRON TRANSFER REACTIONS OF SILICON SUBSTITUTED HETEROATOM COMPOUNDS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.
  155256. GABRIEL WEATHERHEAD
  155257. 7853N
  155258. 2/28/96V
  155259. ANDO, WATARU. SYNTHESIS AND STRUCTURES OF FUNCTIONALIZED CYCLOPOLYSILANES AND RELATED COMPOUNDS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155260. GABRIEL WEATHERHEAD
  155261. 7854N
  155262. 2/28/96
  155263. 4TOYOTA, KOZO; YOSHIFUJI, MASAAKI. EXTREMELY BULKY LITHIUM TRIALKYLSILYL (2,4,6 TRI T BUTYLPHENYL)PHOSPHIDES. SYNTHETIC APPLICATIONS TO STERICALLY PROTECTED PHOSPHAETHYLENES, PHOSPHAALLENES, AND RELATED COMPOUNDS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.
  155264. GABRIEL WEATHERHEAD
  155265. 7855N
  155266. 2/28/96V
  155267. YAGUPOLSKY, YURI L. YLIDES STABILIZED BY (FLUORO, PERFLUOROALKYL) SULFONYL GROUPS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155268. GABRIEL WEATHERHEAD
  155269. 7856N
  155270. 2/28/96V
  155271. OHTA, HIROMICHI. MICROBIAL OXIDATION OF ORGANIC SULFUR COMPOUNDS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155272. GABRIEL WEATHERHEAD
  155273. 7857N
  155274. 2/28/96V
  155275. OGURA, KATSUYUKI. HOW DOES THE COMBINATION OF A THIO GROUP AND A SULFONYL GROUP CONTRIBUTE TO ORGANIC SYNTHESIS?  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155276. GABRIEL WEATHERHEAD
  155277. 7858N
  155278. 2/28/96V
  155279. KATRITZKY, ALAN R.; KARELSON, MATI; HITCHINGS, GREGORY J. CYCLOADDITIONS OF SIX MEMBERED HETEROAROMATIC BETAINES.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155280. GABRIEL WEATHERHEAD
  155281. 7859N
  155282. 2/28/96V
  155283. NOJIMA, MASATOMO. CHEMISTRY OF CARBONYL OXIDES GENERATED FROM THE OZONOLYSIS OF VINYL ETHERS.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155284. GABRIEL WEATHERHEAD
  155285. 7860N
  155286. 2/28/96V
  155287. ARBUZOV, BORIZ A. OUR PATH IN SCIENCE.  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 5, SHIGERU OAE, ED., MYU TOKYO, JAPAN, 1991. A REVIEW.a
  155288. GABRIEL WEATHERHEAD
  155289. 7861N
  155290. 2/28/96V
  155291. ANTKOWIAK, ROZA; ANTKOWIAK, WIESLAW. ALKALOIDS FROM MUSHROOMS.  THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY.VOLUME 40, A. BROSSI, ED., ACADEMIC PRESS: NEWYORK, 1991. A REVIEW.a
  155292. GABRIEL WEATHERHEAD
  155293. 7862N
  155294. 2/28/96
  155295. VERPOORTE, ROBERT; VAN DER HEIDEN, ROBERT, VAN GULIK, WALTER M.; TEN HOOPEN, HENS J. G. PLANT BIOTECHNOLOGY FOR THE PRODUCTION OF ALKALOIDS: PRESENT STATUS AND PROSPECTS.  THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY.VOLUME 40, A. BROSSI, ED., ACADEMIC PRESS: NEWYORK, 1991. A REVIEW.
  155296. GABRIEL WEATHERHEAD
  155297. 7863N
  155298. 2/28/96VuISAACS, NEIL S. THE ROLE OF HIGH PRESSURE METHODS IN ORGANIC CHEMISTRY. TETRAHEDRON, 1991, 47(40), 8463 97. A REVIEW.a
  155299. GABRIEL WEATHERHEAD
  155300. 7864N
  155301. 2/28/96V`KUTYREV, A. A. NUCLEOPHILIC REACTIONS OF QUINONES. TETRAHEDRON, 1991, 47(38), 8043 65. A REVIEW.a
  155302. GABRIEL WEATHERHEAD
  155303. 7865N
  155304. 2/28/96V
  155305. THUMMEL, RANDOLPH P. THE SYNTHESIS AND PROPERTIES OF ORGANIZED POLYAZA CAVITY SHAPED MOLECULES. TETRAHEDRON, 1991, 47(34), 6851 86. A REVIEW.a
  155306. GABRIEL WEATHERHEAD
  155307. 7866N
  155308. 2/28/96V
  155309. CINTAS, P. ASYMMETRIC SYNTHESIS OF ALPHA AMINO ACIDS FROM CARBOHYDRATES AS CHIRAL TEMPLATES. TETRAHEDRON, 1991, 47(32), 6079 111. A REVIEW.a
  155310. GABRIEL WEATHERHEAD
  155311. 7867N
  155312. 2/28/96
  155313. CROCKETT, NIGEL; ALEFOUNDER, PETER R.; BATTERSBY, ALAN R.; ABELL, CHRIS. UROPORPHYRINOGEN III SYNTHASE: STUDIES ON ITS MECHANISM OF ACTION, MOLECULAR BIOLOGY AND BIOCHEMISTRY. TETRAHEDRON, 1991, 47(31), 6003 14. A REVIEW.a
  155314. GABRIEL WEATHERHEAD
  155315. 7868N
  155316. 2/28/96V
  155317. KUTCHAN, T. M.; DITTRICH, H.; BRACHER, D.; ZENK, M. H. ENZYMOLOGY AND MOLECULAR BIOLOGY OF ALKALOID BIOSYNTHESIS. TETRAHEDRON, 1991, 47(31), 5945 54. A REVIEW.a
  155318. GABRIEL WEATHERHEAD
  155319. 7869N
  155320. 2/28/96V
  155321. PETRAGNANI, N.; COMASSETO, J. V. TELLURIUM REAGENTS IN ORGANIC SYNTHESIS; RECENT ADVANCES. PART 1. SYNTHESIS, 1991, (10), 793 817. A REVIEW.a
  155322. GABRIEL WEATHERHEAD
  155323. 7870N
  155324. 2/28/96V|OTSUKA, SEI; TANI, KAZUHIDE. CATALYTIC ASYMMETRIC HYDROGEN MIGRATION OF ALLYLAMINES. SYNTHESIS, 1991, (9), 665 80. A REVIEW.a
  155325. GABRIEL WEATHERHEAD
  155326. 7871N
  155327. 2/28/96
  155328. CVvGOKEL, GEORGE W.; MEDINA, JULIO C.; LI, CHENSHENG. PROPERTY DIRECTED SYNTHESIS. SYNLETT, 1991, (10), 677 83. A REVIEW.a
  155329. GABRIEL WEATHERHEAD
  155330. 7872N
  155331. 2/28/96V
  155332. KING, R. B. PHOSPHORUS BRIDGING CARBONYL DERIVATIVES: ORGANOPHOSPHORUS ANALOGS OF ALDEHYDES AND KETONES. SYNLETT, 1991, (10), 671 6. A REVIEW.a
  155333. GABRIEL WEATHERHEAD
  155334. 7873N
  155335. 2/28/96VeFUJI, K.; NODE, M. CHIRAL NITRO OLEFINS FOR ENANTIOSELECTIVE REACTIONS. 1991, (10), 603 10. A REVIEW.a
  155336. GABRIEL WEATHERHEAD
  155337. 7874N
  155338. 2/28/96V
  155339. FERGUSON, RICHARD R.; KRAJNIK, PAUL; CRABTREE, ROBERT H. THE DEVELOPMENT OF MERCURY PHOTOSENSITIZED REACTIONS FOR FUNCTIONALIZING UNACTIVATED CARBON HYDROGEN BONDS IN ORGANIC COMPOUNDS. SYNLETT, 1991, (9), 597 603. A REVIEW.a
  155340. GABRIEL WEATHERHEAD
  155341. 7875N
  155342. 2/28/96V
  155343. TRZHTSINSKAYA, B. V.; ABRAMOVA, N. D. IMIDAZOLE  THIONES: SYNTHESIS, STRUCTURE, PROPERTIES. SULFUR REPORTS, 1991, 10(4), 389 430. A REVIEW.a
  155344. GABRIEL WEATHERHEAD
  155345. 7876N
  155346. 2/28/96VxMASHKINA, A. V. CATALYTIC SYNTHESIS OF SULFIDES, SULFOXIDES AND SULFONES. SULFUR REPORTS, 1991,10(4), 279 388. A REVIEW.a
  155347. GABRIEL WEATHERHEAD
  155348. 7877N
  155349. 2/28/96V
  155350. TOLSTIKOV, G. A.; BORISOVA, E. YA; CHERKASHIN, M. I.; KOMAROV, V. M.; ARZAMASTSEV, E. V. SYNTHESIS AND REACTIVITY OF N SUBSTITUTED AMINOAMIDES, ANTIARRYTHMIC AND LOCAL ANESTHETIC ACTIVITY. RUSSIAN CHEM REV, 1991, 60(4), 420 34. A REVIEW.a
  155351. GABRIEL WEATHERHEAD
  155352. 7878N
  155353. 2/28/96VmKOLODYAZHNYI, O. I. P HALOGEN SUBSTITUTED PHOSPHORUS YLIDS. RUSSIAN CHEM REV, 1991, 60(4), 391 409. A REVIEW.a
  155354. GABRIEL WEATHERHEAD
  155355. 7879N
  155356. 2/28/96V
  155357. LERMAN B. M. SKELETAL REARRANGEMENTS IN CAGE COMPOUNDS WITH MEDIUM SIZED RINGS. RUSSIAN CHEM REV, 1991, 60(4), 736 63. A REVIEW.a
  155358. GABRIEL WEATHERHEAD
  155359. 7880N
  155360. 2/28/96
  155361. KALININ, V. N. FUNCTIONALIZATION OF HETEROCYCLES BY NI AND PD CATALYZED REACTIONS. RUSSIAN CHEM REV, 1991, 60(2),173 91. A REVIEW.a
  155362. GABRIEL WEATHERHEAD
  155363. 7881N
  155364. 2/28/96V
  155365. DIANOVA, E. N., ZABOTINA, E. YA. COMPOUNDS OF DICOORDINATE ARSENIC: CHEMICAL PROPERTIES. RUSSIAN CHEM REV, 1991, 60(2), 162 72. A REVIEW.a
  155366. GABRIEL WEATHERHEAD
  155367. 7882N
  155368. 2/28/96VsGUSAR, N. I. SYNTHESIS OF HETEROCYCLES BY THE AZA WITTIG REACTION. RUSSIAN CHEM REV, 1991, 60(2), 146 61. A REVIEW.a
  155369. GABRIEL WEATHERHEAD
  155370. 7883N
  155371. 2/28/96Vi RAIFEL'D, YU E.; VAISMAN, A. M. ASYMMETRIC EPOXIDATION. RUSSIAN CHEM REV, 1991, 60(2), 123 45. A REVIEW.a
  155372. GABRIEL WEATHERHEAD
  155373. 7884N
  155374. 2/28/96V
  155375. BIEMANN, KLAUS. ANALYTICAL TECHNIQUES FOR TRACE ORGANIC COMPOUNDS. III. MASS SPECTROMETRY IN TRACE ORGANIC ANALYSIS. PURE AND APPLIED CHEM, 1991, 63(11), 1637 46. A REVIEW.a
  155376. GABRIEL WEATHERHEAD
  155377. 7885N
  155378. 2/28/96
  155379. HAAS, ALOIS. PERIODIC SYSTEM OF FUNCTIONAL GROUPS: FORMALISM ONLY OR HEURISTIC PRINCIPLES. PURE AND APPLIED CHEM, 1991, 63(11),1577 90. A REVIEW.a
  155380. GABRIEL WEATHERHEAD
  155381. 7886N
  155382. 2/28/96V
  155383. BARTON, DEREK, H. R.; DOLLER, DARIO. THE SELECTIVE FUNCTIONALIZATION OF SATURATED HYDROCARBONS: GIF ALL THAT. PURE AND APPLIED CHEM, 1991, 63(11), 1567 76. A REVIEW.a
  155384. GABRIEL WEATHERHEAD
  155385. 7887N
  155386. 2/28/96
  155387. DANIL DE NAMOR, ANGELA F.; RITT, MARIE CLAUDE; LEWIS, DAVID F. V.; SCHWING WEILL, MARIE JOSE; NEW, FRANCOISE ARNAUD. SOLUTION THERMODYNAMICS OF AMINO ACID 18 CROWN 6 AND AMINO ACID CRYPTAND 222 COMPLEXATION REACTIONS. PURE AND APPLIED CHEM, 1991, 63(10), 1435 9. A REVIEW.
  155388. GABRIEL WEATHERHEAD
  155389. 7888N
  155390. 2/28/96V
  155391. SHANZER, A.; YAKIREVITCH, P.; GOTTLIEB, H.; TOR, Y.; LIBMAN, J. POLYTOPIC CHIRAL BINDERS. PURE AND APPLIED CHEM, 1990, 62(6),1111 14. A REVIEW.a
  155392. GABRIEL WEATHERHEAD
  155393. 7889N
  155394. 2/28/96
  155395. ABRAMOVITCH, RUDOLPH A. APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A. ORG PREP AND PROC INT, 1991, 23(6), 683 711. A REVIEW.a
  155396. GABRIEL WEATHERHEAD
  155397. 7890N
  155398. 2/28/96V
  155399. KOTALI, ANTIGONI; PAPAGEORGIOU, VASSILIOS P. THE CHEMISTRY OF 1,3 DIOXIMES. ORG PREP AND PROC INT, 1991, 23(5), 593 610. A REVIEW.a
  155400. GABRIEL WEATHERHEAD
  155401. 7891N
  155402. 2/28/96V
  155403. COSSU, SERGIO; DE LUCCHI, OTTORINO; FABBRI, DAVIDE; LICINI, GIULIA; PASQUATO,LUCIA. 1,2 BIS(ARYLSULFONYL)ALKENES. ORG PREP AND PROC INT, 1991, 23(5), 571 92. A REVIEW.a
  155404. GABRIEL WEATHERHEAD
  155405. 7892N
  155406. 2/28/96V]YUNUSOV, M. S. DITERPENOID ALKALOIDS. NATURAL PRODUCT REPORTS, 1991, 8(5), 499 526. A REVIEW.a
  155407. GABRIEL WEATHERHEAD
  155408. 7893N
  155409. 2/28/96V`KERR, R. G.; BAKER, B. J. MARINE STEROLS. NATURAL PRODUCT REPORTS, 1991, 8(5), 465 97. A REVIEW.a
  155410. GABRIEL WEATHERHEAD
  155411. 7894N
  155412. 2/28/96
  155413. ZV\AYER, W. A. THE LYCOPODIUM ALKALOIDS. NATURAL PRODUCT REPORTS, 1991, 8(5), 455 63. A REVIEW.a
  155414. GABRIEL WEATHERHEAD
  155415. 7895N
  155416. 2/28/96VoBEALE, M. H. BIOSYNTHESIS OF C5 C20 TERPENOID COMPOUNDS. NATURAL PRODUCT REPORTS, 1991, 8(5), 441 54. A REVIEW.a
  155417. GABRIEL WEATHERHEAD
  155418. 7896N
  155419. 2/28/96V
  155420. ZAMAN, SYED S.; SHARMA, RAM P. SOME ASPECTS OF THE CHEMISTRY AND BIOLOGICAL ACTIVITY OF ARTEMISININ AND RELATED ANTIMALARIALS. HETEROCYCLES, 1991, 32(8),1593 638. A REVIEW.a
  155421. GABRIEL WEATHERHEAD
  155422. 7897N
  155423. 2/28/96V
  155424. ALVAREZ, MERCEDES; SALAS, MARISA; JOULE, JOHN A. MARINE NITROGEN CONTAINING HETEROCYCLIC NATURAL PRODUCTS. STRUCTURES AND SYNTHESES OF COMPOUNDS CONTAINING INDOLE UNITS. HETEROCYCLES, 1991, 32(7), 1391 429. A REVIEW.a
  155425. GABRIEL WEATHERHEAD
  155426. 7898N
  155427. 2/28/96VnSNIDER,BARRY. CARBOFUNCTIONALIZATION OF ALKENES. CHEMTRACTS: ORGANIC CHEMISTRY, 1991, 4(6), 403 419. A REVIEW.a
  155428. GABRIEL WEATHERHEAD
  155429. 7899N
  155430. 2/28/96V
  155431. BOGER, DALE L. DUOCARMYCINS: A NEW CLASS OF SEQUENCE SELECTIVE DNA MINOR GROOVE ALKYLATING AGENTS. CHEMTRACTS: ORGANIC CHEMISTRY, 1991, 4(5), 329 49. A REVIEW.a
  155432. GABRIEL WEATHERHEAD
  155433. 7900N
  155434. 2/28/96V
  155435. YAMAMOTO, YOSHINORI. A NEW ENTRY INTO CARBANION CHEMISTRY. NEW SELECTIVITIES AND REACTIVITIES VIA STABILIZATION ACTIVATION PROCEDURE OF ANIONIC SPECIES WITH GROUP 14 ORGANOMETALLICS. CHEMTRACTS: ORGANIC CHEMISTRY, 1991, 4(4), 255 71. A REVIEW.a
  155436. GABRIEL WEATHERHEAD
  155437. 7901N
  155438. 2/28/96VjHOULTON, SARAH. FK506 AND ORGAN TRANSPLANTS. CHEMISTRY AND INDUSTRY (LONDON), 1991, (11), 386 7. A REVIEW.a
  155439. GABRIEL WEATHERHEAD
  155440. 7902N
  155441. 2/28/96V
  155442. LEWIS, NORMAN; MITCHELL, MICHAEL. DRUG PROCESS RESEARCH AND DEVELOPMENT. CHEMISTRY AND INDUSTRY (LONDON), 1991, (11), 374 8. A REVIEW.a
  155443. GABRIEL WEATHERHEAD
  155444. 7903N
  155445. 2/28/96
  155446. cV}LEE, ROB. BUCKMINSTERFULLERENE: THE THIRD ALLOTROPE OF CARBON. CHEMISTRY AND INDUSTRY (LONDON), 1991, (10), 349 50. A REVIEW.a
  155447. GABRIEL WEATHERHEAD
  155448. 7904N
  155449. 2/28/96VaMOODY, ANDREW. FULLERENE CHEMISTRY. CHEMISTRY AND INDUSTRY (LONDON), 1991, (10), 346 7. A REVIEW.a
  155450. GABRIEL WEATHERHEAD
  155451. 7905N
  155452. 2/28/96VnREHOREK, DETLEF. SPIN TRAPPING OF INORGANIC RADICALS. CHEMICAL SOCIETY REVIEWS, 1991, 20(3), 341 53. A REVIEW.a
  155453. GABRIEL WEATHERHEAD
  155454. 7906N
  155455. 2/28/96V
  155456. DAVIES, H. GEOFFREY; GREEN, RICHARD H. AVERMECTINS AND MILBEMYCINS. PART II. CHEMICAL SOCIETY REVIEWS, 1991, 20(3), 271 339. A REVIEW.a
  155457. GABRIEL WEATHERHEAD
  155458. 7907N
  155459. 2/28/96V
  155460. IZATT, REED M.; PAWLAK, KRYSTYNA; BRADSHAW, JERALD S.; BRUENING, RONALD L. THERMODYNAMIC AND KINETIC DATA FOR MACROCYCLE INTERACTIONS WITH CATIONS AND ANIONS. CHEMICAL REVIEWS, 1991, 91(8), 1721 85. A REVIEW.a
  155461. GABRIEL WEATHERHEAD
  155462. 7908N
  155463. 2/28/96
  155464. MAZZUCATO, UGO; MOMICCHIOLI, FABIO. ROTATIONAL ISOMERISM IN TRANS 1,2 DIARYLETHYLENES. CHEMICAL REVIEWS, 1991, 91(8),1679 719. A REVIEW.a
  155465. GABRIEL WEATHERHEAD
  155466. 7909N
  155467. 2/28/96VmCREARY, XAVIER. ELECTRONEGATIVELY SUBSTITUTED CARBOCATIONS. CHEMICAL REVIEWS, 1991, 91 (8),1625 78. A REVIEW.a
  155468. GABRIEL WEATHERHEAD
  155469. 7910N
  155470. 2/28/96VjPARKER, DAVID. NMR DETERMINATION OF ENANTIOMERIC PURITY. CHEMICAL REVIEWS, 1991, 91(7), 1441 57. A REVIEW.a
  155471. GABRIEL WEATHERHEAD
  155472. 7911N
  155473. 2/28/96VqHORVATH, ISTVAN T.; MILLAR, JOHN M. NMR UNDER HIGH GAS PRESSURE. CHEMICAL REVIEWS, 1991, 91(7),1339 51. A REVIEW.a
  155474. GABRIEL WEATHERHEAD
  155475. 7912N
  155476. 2/28/96V
  155477. HIRSCHMANN, RALPH. MEDICINAL CHEMISTRY IN THE GOLDEN AGE OF BIOLOGY. LESSONS FROM STEROID AND PEPTIDE RESEARCH. ANGEW CHEMIE INT ED ENG, 1991, 30(10), 1278 1301. A REVIEW.a
  155478. GABRIEL WEATHERHEAD
  155479. 7913N
  155480. 2/28/96
  155481. KENNARD, OLGA; HUNTER, WILLIAM N. SINGLE CRYSTAL X RAY STRUCTURE ANALYSIS OF OLIGONUCLEOTIDES AND THEIR COMPLEXES. ANGEW CHEMIE INT ED ENG, 1991, 30(10), 1254 77. A REVIEW.a
  155482. GABRIEL WEATHERHEAD
  155483. 7914N
  155484. 2/28/96V
  155485. VON SONNTAG, CLEMENS; SCHUCHMANN, HEINZ PETER. ELUCIDATION OF PEROXYL RADICAL REACTIONS IN AQUEOUS SOLUTION WITH RADIATION CHEMISTRY TECHNOLOGY. ANGEW CHEMIE INT ED ENG, 1991, 30(10),1229 53. A REVIEW.a
  155486. GABRIEL WEATHERHEAD
  155487. 7915N
  155488. 2/28/96V
  155489. RAMOS TOMBO, GERARDO M.; BELLUS, DANIEL. CHIRALITY AND CROP PROTECTION. ANGEW CHEMIE INT ED ENG, 1991, 30(10),1193 1215. A REVIEW.a
  155490. GABRIEL WEATHERHEAD
  155491. 7916N
  155492. 2/28/96VqHOPF, H. ATOMS AND REACTIVE MOLECULES IN A CLOSED SYSTEM. ANGEW CHEMIE INT ED ENG, 1991, 30(9), 1117 8. A REVIEW.a
  155493. GABRIEL WEATHERHEAD
  155494. 7917N
  155495. 2/28/96
  155496. BURSTEN, BRUCE E.; STRITTMATTER, RICHARD J. CYCLOPENTADIENYL COMPLEXES OF ACTINIDES FORMATION AND ELECTRON CONFIGURATION. ANGEW CHEMIE INT ED ENG, 1991, 30(9), 1069 85. A REVIEW.a
  155497. GABRIEL WEATHERHEAD
  155498. 7918N
  155499. 2/28/96V
  155500. VOEGTLE, FRITZ; KNOPS, PETER. PIGMENTS FOR VISUAL DIFFERENTIATION OF ENANTIOMERS: CROWN ETHERS AS OPTICAL SENSORS FOR CHIRAL COMPOUNDS. ANGEW CHEMIE INT ED ENG, 1991, 30(8), 958 60. A REVIEW.a
  155501. GABRIEL WEATHERHEAD
  155502. 7919N
  155503. 2/28/96V
  155504. KOELLE, ULRICH. ENERGETIC AND CONSTITUTIONAL HYSTERESIS IN BISTABLE MOLECULES. ANGEW CHEMIE INT ED ENG, 1991, 30(8), 956 8. A REVIEW.a
  155505. GABRIEL WEATHERHEAD
  155506. 7920N
  155507. 2/28/96
  155508. TSUMURAYA, TAKESHI; BATCHELLER, SCOTT A.; MASAMUNE, SATORU. COMPOUNDS WITH SILICON SILICON, GERMANIUM GERMANIUM, AND TIN TIN DOUBLE BONDS IN ADDITION TO STRAINED RING SYSTEMS WITH THE SILICON , GERMANIUM , AND TIN FRAMEWORK. ANGEW CHEMIE INT ED ENG, 1991, 30(8), 902 30. A REVIEW.
  155509. GABRIEL WEATHERHEAD
  155510. 7921N
  155511. 2/28/96VmWILLIAMS, DUDLEY H. THE MOLECULAR BASIS OF BIOLOGICAL ORDER. ALDRICHIMICA ACTA, 1991, 24(3), 71 80. A REVIEW.a
  155512. GABRIEL WEATHERHEAD
  155513. 7922N
  155514. 2/28/96VnGRIECO, PAUL A. ORGANIC CHEMISTRY IN UNCONVENTIONAL SOLVENTS. ALDRICHIMICA ACTA, 1991, 24(3), 59 66. A REVIEW.a
  155515. GABRIEL WEATHERHEAD
  155516. 7923N
  155517. 2/28/96V
  155518. DESLONGCHAMPS, PIERRE. TRANSANNULAR DIELS ALDER REACTION ON MACROCYCLES: A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYCYCLIC COMPOUNDS. ALDRICHIMICA ACTA, 1991, 24(2), 43 56. A REVIEW.a
  155519. GABRIEL WEATHERHEAD
  155520. 7924N
  155521. 2/28/96V
  155522. SILVESTER, MICHAEL J. FLUOROHETEROCYCLIC COMPOUNDS: SYNTHESIS, REACTIONS AND COMMERCIAL APPLICATIONS. ALDRICHIMICA ACTA, 1991, 24(2), 31 38. A REVIEW.a
  155523. GABRIEL WEATHERHEAD
  155524. 7925N
  155525. 2/28/96
  155526. QUEGUINER, GUY; MARSAIS, FRANCIS; SNIECKUS, VICTOR; EPSZTAJN, JAN. DIRECTED METALATION AND PI DEFICIENT AZAAROMATICS: STRATEGIES OF FUNCTIONALIZATION OF PYRIDINES, QUINOLINES, AND DIAZINES. ADVANCES IN HETEROCYCLIC CHEM, 1991, 52,189 295. A REVIEW.a
  155527. GABRIEL WEATHERHEAD
  155528. 7926N
  155529. 2/28/96V
  155530. HAZAI, LASZLO. 3(2H) ISOQUINOLONES AND THEIR SATURATED DERIVATIVES. ADVANCES IN HETEROCYCLIC CHEM, 1991, 52, 156 188. A REVIEW.a
  155531. GABRIEL WEATHERHEAD
  155532. 7927N
  155533. 2/28/96V
  155534. SHABAN, MOHAMMED A. E.; TAHA, MAMDOUH A. M.; SHARSHIRA, ESSAM M. SYNTHESIS AND BIOLOGICAL ACTIVITIES OF CONDENSED HETEROCYCLO[N,M A, B, OR C]QUINAZOLINES. ADVANCES IN HETEROCYCLIC CHEM, 1991, 52, 5 155. A REVIEW.a
  155535. GABRIEL WEATHERHEAD
  155536. 7928N
  155537. 2/28/96V
  155538. KAZANSKII, VLADIMIR B. THE NATURE OF ADSORBED CARBENIUM IONS AS ACTIVE INTERMEDIATES IN CATALYSIS BY SOLID ACIDS. ACCTS OF CHEM RESEARCH 1991, 24(12), 379 83. A REVIEW.a
  155539. GABRIEL WEATHERHEAD
  155540. 2/28/96V^BOWEN,RICHARD D. ION NEUTRAL COMPLEXES. ACCTS OF CHEM RESEARCH 1991, 24(12), 364 71. A REVIEW.a
  155541. GABRIEL WEATHERHEAD
  155542. 7930N
  155543. 2/28/96V
  155544. STEIN, STEPHEN E. THERMAL REACTIONS AND PROPERTIES OF POLYCYCLIC AROMATIC. ACCTS OF CHEM RESEARCH 1991, 24(11), 350 6. A REVIEW.a
  155545. GABRIEL WEATHERHEAD
  155546. 7931N
  155547. 2/28/96VWSTELIOU, KOSTA. DIATOMIC SULFUR. ACCTS OF CHEM RESEARCH 1991, 24(11), 341 50. A REVIEW.a
  155548. GABRIEL WEATHERHEAD
  155549. 7932N
  155550. 2/28/96VjTYLER, DAVID R. 19 ELECTRON ORGANOMETALLIC ADDUCTS. ACCTS OF CHEM RESEARCH 1991, 24(11), 325 31. A REVIEW.a
  155551. GABRIEL WEATHERHEAD
  155552. 7933N
  155553. 2/28/96V|STANG, PETER J. ALKYNYL CARBOXYLATE, PHOSPHATE, AND SULFONATE ESTERS. ACCTS OF CHEM RESEARCH 1991, 24(10), 304 10. A REVIEW.a
  155554. GABRIEL WEATHERHEAD
  155555. 7934N
  155556. 2/28/96
  155557. PORTER, NED A.; GIESE, BERND; CURRAN, DENNIS P. ACYCLIC STEREOCHEMICAL CONTROL IN FREE RADICAL REACTIONS. ACCTS OF CHEM RESEARCH 1991, 24(10), 296 304. A REVIEW.a
  155558. GABRIEL WEATHERHEAD
  155559. 7935N
  155560. 2/28/96VkRAGNARSSON, ULF; GREHN, LEIF. NOVEL GABRIEL REAGENTS. ACCTS OF CHEM RESEARCH 1991, 24(10), 285 9. A REVIEW.a
  155561. GABRIEL WEATHERHEAD
  155562. AUST J CHEMC
  155563. CLAISEN REARRANGEMENT (+/ ) 4 DEMETHOXYDAUNOMYCINONE HYDROXYANTHRAQUINONES MICROMONOSPORA INTERMEDIATE DAUNOMYCIN ADRIAMYCIN CAMBIE RCM
  155564. 7936N
  155565. 2/28/96V=SYNTHETIC ANTHRACYCLINES FROM ANTHRAQUINONES   INVITED REVIEWW
  155566. 1992X
  155567. 483 512Y
  155568. 45(3)a
  155569. GABRIEL WEATHERHEAD
  155570. B ASPECTS OF HOMOGENEOUS CATALYSISC
  155571. NOELS FISCHER LIGAND INSERTION SYNTHETIC REVIEW CARBENE YLIDE RHODIUM APPLICATIONS TRANSITION CARBENOID CYCLOADDITION CHROMIUM METAL ALKYLIDENE TITANIUM CATALYSIS DIAZO CYCLOPROPANATION COPPERM
  155572. 7937N
  155573. 2/28/96
  155574. VqRECENT ASPECTS OF TRANSITION METAL CATALYZED REACTIONS OF CARBENES IN THE REALM OF BIOLOGICALLY ACTIVE SUBSTANCESW
  155575. V 6 1988 P 199a
  155576. GABRIEL WEATHERHEAD
  155577. CHEM SOC REVCEREVIEW CARBENOID FISCHER COMPLEX CYCLISATION YLIDE AMINE METAL RUDLERM
  155578. 7938N
  155579. 2/28/96V
  155580. AMINO CARBENE COMPLEXES OF CH AND MO  FOR CASCADE REACTIONS WITH ALKYNES LEADING TO NEW HETEROCYCLIC COMPOUNDS VIA NITROGEN YLIDESW
  155581. VOL 20 1991 P 503a
  155582. GABRIEL WEATHERHEAD
  155583. ACC CHEM RESCOCHIRAL REVIEW ORGANOBORANE ASYMMETRIC BORON PINENE VEERANAGHANAN RAMEICHANAURANM
  155584. 7939N
  155585. 2/28/96VWREVIEW OF ASYMMETRIC REDUCTION OF CARBONYL GROUPS BY BORON REAGENTS BASED UPON A PINENEW
  155586. VOL 25 1992 P 2a
  155587. GABRIEL WEATHERHEAD
  155588. ANGEW CHEM INT ED ENGLCCLOCKHOFF REVIEW GLYCOLIPIDS SYNTHESIS PROPERTIES GLYCOSPHINGOLIPIDSM
  155589. 7940N
  155590. 2/28/96V:GLYCOLIPIDS AS IMMUNOMODULATORS:  SYNTHESIS AND PROPERTIESW
  155591. VOL 30 1990 P 1611a
  155592. GABRIEL WEATHERHEAD
  155593. ANGEW CHEM INT ED ENGL
  155594. C@FREITAG POLYCARBONATE REVIEW STRUCTURE PROPERTY POLYMER MATERIALM
  155595. 7941N
  155596. 2/28/96VGROUTES TO NEW AROMATIC POLYCARBONATES WITH SPECIAL MATERIAL PROPERITIESW
  155597. VOL 30 1991 P 1598a
  155598. GABRIEL WEATHERHEAD
  155599. ANGEW CHEM INT ED ENGLCZGOLDMAN REVIEW SYNTHESIS ENANTIOSELECTIVE DIHYDRO PYRIDINE CHIRALITY CONFORMATION ACTIVITYM
  155600. 7942N
  155601. 2/28/96Vu1,4 DIHYDROPYRIDINES:  EFFECTS OF CHIRALITY AND CONFORMATION ON THE CALCIUM ANTAGONIST AND CALCIUM AGONIST ACTIVITIESW
  155602. VOL 30 1991 P 1559a
  155603. GABRIEL WEATHERHEAD
  155604. ANGEW CHEM INT ED ENGCgREETZ REVIEW AMINO ACID STEREOSELECTIVE DIELS ALDER WITTIG MICHAEL CYCLOADDITION CHIRAL BUILDING BLOCKSM
  155605. 7943N
  155606. 2/28/96VSNEW APPROACHES TO USE OF AMINO ACIDS AS CHIRAL BUILDING BLOCKS IN ORGANIC SYNTHESISW
  155607. VOL 30 1991 P 1531a
  155608. GABRIEL WEATHERHEAD
  155609. ACC CHEM RESCKDIAZO CARBENE SUBSTITUTION CATION MECHANISM ELECTRON TRANSFER REVIEW CREARYM
  155610. 7944N
  155611. 2/28/96
  155612. VMREACTION OF HALODIAZIRIDINES BY SN2 AND ELECTRON TRANSFER INITIATED PROCESSESW
  155613. VOL 25 1992 P 31a
  155614. GABRIEL WEATHERHEAD
  155615. TETRAHEDRONCUSYNTHESIS OXAZIRIDINE REVIEW RING LACTAM HETEROCYCLE ANNULATION NITROGEN MEDIUM EVANSM
  155616. 7945N
  155617. 2/28/96V!MEDIUM RING NITROGEN HETEROCYCLESW
  155618. VOL 47 1991 P 9131a
  155619. GABRIEL WEATHERHEAD
  155620. TET LETTCGEPOXIDE AMINE AZIRIDINE PAYNE REARRANGEMENT SULFONAMIDE REVIEW MOULINESM
  155621. 7946N
  155622. 2/28/96VGPAYNE LIKE REARRANGEMENT OF TOSYL EPOXIDES TO FUNCTIONALIZED AZIRIDINESW
  155623. 1992 P 487a
  155624. GABRIEL WEATHERHEAD
  155625. CHEMTRACTSCYREVIEW 2+2 KETENE CYCLOBUTANONE INTRAMOLECULAR VINYL MANGANESE RADICAL CYCLIZATION SNIDERM
  155626. 7947N
  155627. 2/28/96VbCARBOFUNCTIONALIZATION OF ALKENES BY INTRAMOLECULAR 2+2 CYCLOADDITIONS OF AND MN (II) CYCLIZATIONSW
  155628. 1991 P 403a
  155629. GABRIEL WEATHERHEAD
  155630. EXPERIENTIACNJERINA NIH SHIFT ARENE OXIDE HYDROGEN BIOLOGICAL REVIEW WITKOP BENZENE EPOXIDEM
  155631. 7948N
  155632. 2/28/96
  155633. VcARENE OXIDES AND THE NIH SHIFT.  THE METABOLISM, TOXICITY AND CARCINOGENICITY OF AROMATIC COMPOUNDSW
  155634. VOL 28 1972 P1129a
  155635. GABRIEL WEATHERHEAD
  155636. J ORG CHEMC=EPOXIDE RING OPENING TIN STANNYL CUPRATE HYDRIDE REVIEW CHONGM
  155637. 7949N
  155638. 2/28/96VWRING OPENING REACTIONS OF ALPHA STANNYL EPOXIDES WITH METAL HYDRIDES AND ORGANOCUPRATESW
  155639. VOL 57 1992 P46a
  155640. GABRIEL WEATHERHEAD
  155641. JACSC[FISCHER CHROMIUM CARBENE WRITING REVIEW INTRODUCTION CYCLIZATION TANDEM KETENE PHENOL WULFFM
  155642. 7950N
  155643. 2/28/96V
  155644. TANDEM DIELS ALDER DOUBLE INTRAMOLECULAR TWO ALKYNE ANNULATIONS OF FISCHER CARBENE COMPLEXES.  A ONE POT CONSTRUCTION OF ALL FOUR RINGS OF A STEROID SYSTEMW
  155645. V 113 1991 P 9873a
  155646. GABRIEL WEATHERHEAD
  155647. ACC CHEM RESC^CATION REVIEW CARBONIUM ION NOVEL BRIDGEHEAD BICYCLIC INSIDE OUTSIDE MCMURRY COUPLING TITANIUMM
  155648. 7951N
  155649. 2/28/96V9THREE CENTER, TWO ELECTRON CHC BONDS IN ORGANIC CHEMISTRYW
  155650. V 25 1992 P 47a
  155651. GABRIEL WEATHERHEAD
  155652. ACC CHEM RES
  155653. CJHALO DIAZIRENE EXTRUSION NITROGEN REVIEW RING OPENING CARBENE SIMON CREARYM
  155654. 7952N
  155655. 2/28/96VLREACTIONS OF HALODIAZIRINES BY SN2 AND ELECTRON TRANSFER INITIATED PROCESSESW
  155656. V 25 1992 P 31a
  155657. GABRIEL WEATHERHEAD
  155658. TET LETTCKSULFIDE OXIDATION SULFONE REVIEW REAGENT EXPERIMENTAL OSMIUM N OXIDE PRIEBEM
  155659. 7953N
  155660. 2/28/96V8A FACILE AND SELECTIVE OXIDATION OF SULFIDES TO SULFONESW
  155661. 1991 P 7353a
  155662. GABRIEL WEATHERHEAD
  155663. SYNLETTC`REVIEW COUPLING CROSS PALLADIUM CATALYST SILICON SILYL HYPERVALENT TIN STANNANE HECK ARYL HIYAMAM
  155664. 7954N
  155665. 2/28/96VvHIGHLY SELECTIVE CROSS COUPLING REACTIONS OF ORGANOSILICON COMPOUNDS MEDIATED BY FLUORIDE ION AND A PALLADIUM CATALYSTW
  155666. 1991 P 845a
  155667. GABRIEL WEATHERHEAD
  155668. JACSCUWITTIG THEORY STEREOCHEMISTRY REVIEW WRITING BETAINE PHOSPHOROUS YLIDE GEOMETRY LATHIM
  155669. 7955N
  155670. 2/28/96VSTHEORETICAL STUDY OF THE WITTIG OLEFINATION REACTION TO RATIONALIZE STEREOCHEMISTRYW
  155671. V 114 1992 P 813a
  155672. GABRIEL WEATHERHEAD
  155673. J ORG CHEMC^SIMMONS SMITH CYCLOPROPANATION CYCLOPROPANE ZINC REVIEW WRITING ORGANOMETALLIC REAGENT DENMARKM
  155674. 7956N
  155675. 2/28/96VJA COMPARISON OF CHLOROMETHYL AND IODOMETHYL ZINC CYCLOPROPANATION REAGENTSW
  155676. V 56 1991 P 6974a
  155677. GABRIEL WEATHERHEAD
  155678. 7957N
  155679. 2/28/96V
  155680. FLOSS, HEINZ G.; STROHL, WILLIAM R. GENETIC ENGINEERING OF HYBRID ANTIBIOTICS. A PROGRESS REPORT. TETRAHEDRON 1991, 47(31), PG 6045 58. A REVIEW.a
  155681. GABRIEL WEATHERHEAD
  155682. 7958N
  155683. 2/28/96V
  155684. YONEDA, NORIHIKO. THE COMBINATION OF HYDROGEN FLUORIDE WITH ORGANIC BASES AS FLUORINATION AGENTS. TETRAHEDRON 1991, 47(29), PG 5329 65. A REVIEW.a
  155685. GABRIEL WEATHERHEAD
  155686. 7959N
  155687. 2/28/96V
  155688. CROSBY, JOHN. SYNTHESIS OF OPTICALLY ACTIVE COMPOUNDS: A LARGE SCALE PERSPECTIVE. TETRAHEDRON 1991, 47(27), PG 4789 846. A REVIEW.a
  155689. GABRIEL WEATHERHEAD
  155690. 7960N
  155691. 2/28/96
  155692. V~THOMPSON, CHARLES M.; GREEN, DIANA L. C. RECENT ADVANCES IN DIANION CHEMISTRY. TETRAHEDRON 1991, 47(25), PG 4223 85. A REVIEW.a
  155693. GABRIEL WEATHERHEAD
  155694. 7961N
  155695. 2/28/96V
  155696. CORDELL, GEOFFREY; KINGHORN, A. DOUGLAS. ONE DIMENSIONAL PROTON CARBON CORRELATIONS FOR THE STRUCTURE DETERMINATION OF NATURAL PRODUCTS. TETRAHEDRON 1991, 47(22), PG 3521 34. A REVIEW.a
  155697. GABRIEL WEATHERHEAD
  155698. 7962N
  155699. 2/28/96V
  155700. MIKAMI, KOICHI; NAKAI, TAKESHI. ACYCLIC STEREOCONTROL VIA [2,3] WITTIG SIGMATROPIC REARRANGEMENT. SYNTHESIS 1991, (8), PG 594 604. A REVIEW.a
  155701. GABRIEL WEATHERHEAD
  155702. 7963N
  155703. 2/28/96VyDENINNO, MICHAEL P. THE SYNTHESIS AND GLYCOSIDATION OF N ACETYLNEURAMINIC ACID. SYNTHESIS 1991, (8), PG 583 93. A REVIEW.a
  155704. GABRIEL WEATHERHEAD
  155705. 7964N
  155706. 2/28/96
  155707. DRUECKHAMMER, DALE G.; HENNEN, WILLIAM J.; PEDERSON, RICHARD L.; BARBAS, CARLOS F. III; GAUTHERON, CHRISTINE M.; KRACH, THOMAS; WONG, CHI HUEY. ENZYME CATALYSIS IN SYNTHETIC CARBOHYDRATE CHEMISTRY. SYNTHESIS 1991, (7), PG 499 525. A REVIEW.a
  155708. GABRIEL WEATHERHEAD
  155709. 7965N
  155710. 2/28/96V
  155711. TAMURA, RUI; KAMIMURA, AKIO; ONO, NOBORU. DISPLACEMENT OF ALIPHATIC NITRO GROUPS BY CARBON AND HETEROATOM NUCLEOPHILES. SYNTHESIS 1991, (6), PG 423 34. A REVIEW.a
  155712. GABRIEL WEATHERHEAD
  155713. 7966N
  155714. 2/28/96VhNAKAMURA, EIICHI. NEW TOOLS IN SYNTHETIC ORGANOCOPPER CHEMISTRY. SYNLETT 1991, (8), PG 539 47. A REVIEW.a
  155715. GABRIEL WEATHERHEAD
  155716. 7967N
  155717. 2/28/96V
  155718. MASH, EUGENE A. STEREOCONTROLLED MANIPULATIONS OF CHROMATOGRAPHICALLY RESOLVED PYRANOSIDES. SYNLETT 1991, (8), PG 529 38. A REVIEW.a
  155719. GABRIEL WEATHERHEAD
  155720. 7968N
  155721. 2/28/96VpPHILP, DOUGLAS; STODDART, J. FRASER. SELF ASSEMBLY IN ORGANIC SYNTHESIS. SYNLETT 1991, (7), PG 445 58. A REVIEW.
  155722. GABRIEL WEATHERHEAD
  155723. 7969N
  155724. 2/28/96V
  155725. GROTJAHN, D. B.; DOTZ, K. H. CARBENE COMPLEXES OF CHROMIUM BEARING NITROGEN SUBSTITUENTS. SYNLETT 1991, (6), PG 381 90. A REVIEW.a
  155726. GABRIEL WEATHERHEAD
  155727. 7970N
  155728. 2/28/96
  155729. ASTRUC, DIDIER. THE TRANSFORMATION OF AROMATICS INTO REGIO  AND STEREOCONTROLLED HETEROBIFUNCTIONAL CYCLOHEXADIENES MEDIATED BY TEMPORARY SANDWICH COMPLEXATION. ROLES OF ELECTRON, PROTON, HYDRIDE AND HYDROGEN ATOM TRANSFERS. SYNLETT 1991, (6), PG 369 80. A REVIEW.
  155730. GABRIEL WEATHERHEAD
  155731. 7971N
  155732. 2/28/96V
  155733. PANETTA, CHARLES A.; HEIMER, NORMAN E.; HUSSEY, CHARLES L.; METZGER, ROBERT M. FUNCTIONALIZED TETRACYANOQUINODIMETHANE TYPE ELECTRON ACCEPTORS: SUITABLE PRECURSORS FOR MATERIALS. SYNLETT 1991, (5), PG 301 309. A REVIEW.a
  155734. GABRIEL WEATHERHEAD
  155735. 7972N
  155736. 2/28/96
  155737. GRIBBLE, GORDON W. APPROACHES TO THE SYNTHESIS OF THE ANTITUMOR PYRIDOCARBAZOLE ALKALOIDS. SYNLETT 1991, (5), PG 289 300. A REVIEW.a
  155738. GABRIEL WEATHERHEAD
  155739. 7973N
  155740. 2/28/96V
  155741. ROSEN, TERRY; NAGEL, ARTHUR A.; RIZZI, JAMES P. NOVEL SEROTONIN 3 RECEPTOR ANTAGONISTS. SYNLETT 1991, (4), PG 213 21. A REVIEW.a
  155742. GABRIEL WEATHERHEAD
  155743. 7974N
  155744. 2/28/96V
  155745. BARRY, CLIF E. III; BATES, ROBERT B.; BEAVERS, WIILIAM A.; CAMOU, FERNANDO A.; GORDON, BERNARD, III; HSU, HOWARD F. J.; MILLS, NANCY S.; ET AL. DELOCALIZED CARBANIONS IN SYNTHESIS. SYNLETT 1991, (4), PG 207 12. A REVIEW.a
  155746. GABRIEL WEATHERHEAD
  155747. 7975N
  155748. 2/28/96V
  155749. MANDER, LEWIS N. EXPLOITATION OF ARYL SYNTHONS IN THE SYNTHESIS OF POLYCYCLIC NATURAL PRODUCTS. SYNLETT 1991, (3) PG 134 44. A REVIEW.a
  155750. GABRIEL WEATHERHEAD
  155751. 7976N
  155752. 2/28/96V
  155753. SESSLER, J. L.; CYR, M. J.; BURRELL, A. K. SAPPHYRINS: NEW LIFE FOR AN OLD EXPANDED PORPHYRIN. SYNLETT 1991, (3), PG 127 34. A REVIEW.
  155754. GABRIEL WEATHERHEAD
  155755. 7977N
  155756. 2/28/96VyMARCHAND, ALAN P. POLYCYCLIC CAGE COMPOUNDS AS INTERMEDIATES IN ORGANIC SYNTHESIS. SYNLETT 1991, (2), PG 73 79. A REVIEW.a
  155757. GABRIEL WEATHERHEAD
  155758. 7978N
  155759. 2/28/96VgCURRAN, DENNIS P. RADICAL REACTIONS AND RETROSYNTHETIC PLANNING. SYNLETT 1991, (2), PG 63 72. A REVIEW.a
  155760. GABRIEL WEATHERHEAD
  155761. 7979N
  155762. 2/28/96V
  155763. KUTNEY, JAMES P. PLANT CELL CULTURES AND SYNTHETIC CHEMISTRY
  155764. A POTENTIALLY POWERFUL ROUTE TO COMPLEX NATURAL PRODUCTS. SYNLETT 1991, (1), PG 11 19. A REVIEW.a
  155765. GABRIEL WEATHERHEAD
  155766. 7980N
  155767. 2/28/96V
  155768. HERNDON, JAMES W.; WU, CHAO; HARP, JILL J.; KREUTZER KRISTINA A. EXPLORATION OF THE [3 + 2] CYCLOADDITION REACTION BETWEEN ALLYLSTANNANES AND,UNSATURATED ACYLIRON COMPLEXES. SYNLETT 1991, (1), PG 1 10. A REVIEW.a
  155769. GABRIEL WEATHERHEAD
  155770. 7981N
  155771. 2/28/96
  155772. DUBOIS, JACQUES EMILE; COSSE BARBI, ALIETTE. STRAIN RELEASE IN CONFORMATIONAL AND GEOMETRIC ADAPTATION OF MODERATELY AND HIGHLY CONGESTED SYSTEMS: INTERPLAY OF SMALL STRUCTURAL EFFECTS. STRUCTURAL CHEM 1991, 2, PG 89 105. A REVIEW.a
  155773. GABRIEL WEATHERHEAD
  155774. 7982N
  155775. 2/28/96V
  155776. KLEBE, GERHARD. THE USE OF CRYSTAL DATA TOGETHER WITH OTHER EXPERIMENTAL AND COMPUTATIONAL RESULTS TO DISCUSS STRUCTURE REACTIVITY AND ACTIVITY RELATIONSHIPS. STRUCTURAL CHEM 1990, 1, PG 597 616. A REVIEW.a
  155777. GABRIEL WEATHERHEAD
  155778. 7983N
  155779. 2/28/96V{GREENBERG, ARTHUR; WU, GUANLI. STRUCTURAL RELATIONSHIPS IN SILATRANE MOLECULES. STRUCTURAL CHEM 1990,1, PG 79 85. A REVIEW.a
  155780. GABRIEL WEATHERHEAD
  155781. 7984N
  155782. 2/28/96VsKUTYREV, A. A.; MOSKVA, V. V. NUCLEOPHILIC REACTIONS OF QUINONES. RUSSIAN CHEM REV 1991, 60(1), PG 72 78. A REVIEW.a
  155783. GABRIEL WEATHERHEAD
  155784. 7985N
  155785. 2/28/96
  155786. V{MARETINA, I. A. SYNTHETIC ASPECTS OF THE CHEMISTRY OF UNSATURATED AMINES. RUSSIAN CHEM REV 1991, 60(1), PG 57 71. A REVIEW.a
  155787. GABRIEL WEATHERHEAD
  155788. 7986N
  155789. 2/28/96V
  155790. KHRISTOV, V. KH.; ANGELOV, KH. M.; PETROV, A. A. 1,3ALKADIENES AND THEIR DERIVATIVES IN REACTIONS WITH ELECTROPHILIC REAGENTS. RUSSIAN CHEM REV 1991, 60(1), PG 39 56. A REVIEW.a
  155791. GABRIEL WEATHERHEAD
  155792. 7987N
  155793. 2/28/96V
  155794. BANERJEE, AJOY KUMAR; GONZALEZ, NIEVES CANUDAS. METHODS FOR ANGULAR ALKOXYCARBONYLATION IN FUSED RINGS AND ITS APPLICATION TO THE SYNTHESIS OF TERPENOID COMPOUNDS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS 1991, 110(9), PG 353 67. A REVIEW.a
  155795. GABRIEL WEATHERHEAD
  155796. 7988N
  155797. 2/28/96V
  155798. DOYLE, MICHAEL P. CHIRAL CATALYSTS FOR ENANTIOSELECTIVE CARBENOID CYCLOPROPANATION REACTIONS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS 1991, 110(7 8), PG 305 16. A REVIEW.a
  155799. GABRIEL WEATHERHEAD
  155800. 7989N
  155801. 2/28/96
  155802.     NAEFF, HAN S. D.; FRANSSEN, MAURICE C. R.; VAN DER PLAS, HENK C. QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIP (QSAR) STUDIES OF THE INHIBITION OF XANTHINE OXIDASE BY HETEROCYCLIC COMPOUNDS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS 1991,110(5),PG 139 50. A REVIEW.
  155803. GABRIEL WEATHERHEAD
  155804. 7990N
  155805. 2/28/96V
  155806. ELFERINK, V. H. M.; BREITGOFF, D.; KLOOSTERMAN, M.; KAMPHUIS, J.; VAN DEN TWEEL, W. J. J.; MEIJER, E. M. INDUSTRIAL DEVELOPMENTS IN BIOCATALYSIS. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS 1991,110(3), PG 63 74. A REVIEW.a
  155807. GABRIEL WEATHERHEAD
  155808. 7991N
  155809. 2/28/96V
  155810. SCHOEMAKER, H. E. ON THE CHEMISTRY OF LIGNIN BIODEGRADATION. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS 1990,109(4), PG 255 72. A REVIEW.a
  155811. GABRIEL WEATHERHEAD
  155812. 7992N
  155813. 2/28/96VuKAGAN, J. NATURALLY OCCURRING DI  AND TRITHIOPHENES. PROG CHEM ORGANIC NATURAL PRODUCTS1991, 56, PG 87 169. A REVIEW.a
  155814. GABRIEL WEATHERHEAD
  155815. 2/28/96V
  155816. ASSELINEAU, J. BACTERIAL LIPIDS CONTAINING AMINO ACIDS OR PEPTIDES LINKED BY AMIDE BONDS. PROG CHEM ORGANIC NATURAL PRODUCTS 1991, 56, PG 1 85. A REVIEW.a
  155817. GABRIEL WEATHERHEAD
  155818. 7994N
  155819. 2/28/96V
  155820. PADWA, ALBERT; MURPHREE, S. SHAUN. RECENT DEVELOPMENTS IN THE AREA OF ANNULATED FURANS. ORGANIC PREP AND PROC INT 1991, 23(4), PG 545 68. A REVIEW.a
  155821. GABRIEL WEATHERHEAD
  155822. 7995N
  155823. 2/28/96VxSWINDELL, CHARLES S. TAXANE DITERPENE SYNTHESIS STRATEGIES. ORGANIC PREP AND PROC INT 1991, 23(4), PG 465 543. A REVIEW.a
  155824. GABRIEL WEATHERHEAD
  155825. 7996N
  155826. 2/28/96VoGLOTTER, E. WITHANOLIDES AND RELATED ERGOSTANE TYPE STEROIDS. NATURAL PROD REP 1991, 8(4), PG 415 40. A REVIEW.a
  155827. GABRIEL WEATHERHEAD
  155828. 7997N
  155829. 2/28/96VjMARSTON, A.  HOSTETTMANN, K. MODERN SEPARATION METHODS. NATURAL PROD REP 1991, 8(4), PG 391 413. A REVIEW.a
  155830. GABRIEL WEATHERHEAD
  155831. 7998N
  155832. 2/28/96
  155833. ViBROOKS, C. J. W.; WATSON, D. G. TERPENOID PHYTOALEXINS. NATURAL PROD REP 1991, 8(4), PG 367 89. A REVIEW.a
  155834. GABRIEL WEATHERHEAD
  155835. 7999N
  155836. 2/28/96VxBENTLEY, K. W. ,BETA PHENYLETHYLAMINES AND THE ISOQUINOLINE ALKALOIDS. NATURAL PROD REP 1991, 8(4), PG 339 66. A REVIEW.a
  155837. GABRIEL WEATHERHEAD
  155838. 8000N
  155839. 2/28/96V{JANSEN, B. J. M.; DE GROOT, A. THE SYNTHESIS OF DRIMANE SESQUITERPENOIDS. NATURAL PROD REP 1991, 8(3), PG 319 37. A REVIEW.a
  155840. GABRIEL WEATHERHEAD
  155841. 8001N
  155842. 2/28/96V
  155843. JANSEN, B. J. M.; DE GROOT, A. THE OCCURRENCE AND BIOLOGICAL ACTIVITY OF DRIMANE SESQUITERPENOIDS. NATURAL PROD REP 1991, 8(3), PG 309 18. A REVIEW.a
  155844. GABRIEL WEATHERHEAD
  155845. 8002N
  155846. 2/28/96V
  155847. SAXTON, J. E. RECENT PROGRESS IN THE CHEMISTRY OF INDOLE ALKALOIDS AND MOLD METABOLITES. NATURAL PROD REP 1991, 8(3), PG 251 307. A REVIEW.a
  155848. GABRIEL WEATHERHEAD
  155849. 8003N
  155850. 2/28/96
  155851. V]BRITTON, G. CAROTENOIDS AND POLYTERPENOIDS. NATURAL PROD REP 1991, 8(3), PG 223 49. A REVIEW.a
  155852. GABRIEL WEATHERHEAD
  155853. 8004N
  155854. 2/28/96V
  155855. HERBERT, R. B. THE BIOSYNTHESIS OF PLANT ALKALOIDS AND NITROGENOUS MICROBIAL METABOLITES. NATURAL PROD REP 1991, 8(2), PG 185 209. A REVIEW.a
  155856. GABRIEL WEATHERHEAD
  155857. 8005N
  155858. 2/28/96V
  155859. LEWIS, J. R. MUSCARINE, OXAZOLE, THIAZOLE, IMIDAZOLE, AND PEPTIDE ALKALOIDS, AND OTHER MISCELLANEOUS ALKALOIDS. NATURAL PROD REP 1991, 8(2), PG 171 83. A REVIEW.a
  155860. GABRIEL WEATHERHEAD
  155861. 8006N
  155862. 2/28/96ViDEWICK, P. M. THE BIOSYNTHESIS OF SHIKIMATE METABOLITES. NATURAL PROD REP 1991,8(2), PG 149 70. A REVIEW.a
  155863. GABRIEL WEATHERHEAD
  155864. 8007N
  155865. 2/28/96VVFAULKNER, D. J. MARINE NATURAL PRODUCTS. NATURAL PROD REP 1991, 8(2) 97 147. A REVIEW.a
  155866. GABRIEL WEATHERHEAD
  155867. 8008N
  155868. 2/28/96V]PFANDER, H.; STOLL, H. TERPENOID GLYCOSIDES. NATURAL PROD REP 1991, 8(1), PG 69 95. A REVIEW.
  155869. GABRIEL WEATHERHEAD
  155870. 8009N
  155871. 2/28/96VoMICHAEL, J. P. QUINOLINE, QUINAZOLINE, AND ACRIDONE ALKALOIDS. NATURAL PROD REP 1991, 8(1), PG 53 68. A REVIEW.a
  155872. GABRIEL WEATHERHEAD
  155873. 8010N
  155874. 2/28/96VhTURNER, A. B. STEROIDS: REACTIONS AND PARTIAL SYNTHESIS. NATURAL PROD REP 1991,8(1), PG 17 52. A REVIEW.a
  155875. GABRIEL WEATHERHEAD
  155876. 8011N
  155877. 2/28/96V
  155878. BOX, VERNON G. S. THE ROLE OF LONE PAIR INTERACTIONS IN THE CHEMISTRY OF THE MONOSACCHARIDES. STEREO ELECTRONIC EFFECTS IN UNSATURATED MONOSACCHARIDES. HETEROCYCLES 1991, 32(4) PG 795 807. A REVIEW.a
  155879. GABRIEL WEATHERHEAD
  155880. 8012N
  155881. 2/28/96V
  155882. ALVAREZ, MERCEDES; SALAS, MARISA; JOULE, JOHN A. MARINE NITROGEN CONTAINING HETEROCYCLIC NATURAL PRODUCTS. STRUCTURES AND SYNTHESES OF COMPOUNDS CONTAINING QUINOLINE AND/OR ISOQUINOLINE UNITS. HETEROCYCLES 1991, 32(4), PG 759 94. A REVIEW.a
  155883. GABRIEL WEATHERHEAD
  155884. 8013N
  155885. 2/28/96
  155886. KATRITZKY, ALAN R.; KARELSON, MATI; HARRIS, PHILIP A PROTOTROPIC TAUTOMERISM OF HETEROAROMATIC COMPOUNDS HETEROCYCLES 1991, 32(2), PG 329 69. A REVIEW.a
  155887. GABRIEL WEATHERHEAD
  155888. 8014N
  155889. 2/28/96V
  155890. KATRITZKY, ALAN R.; KARELSON, MATI; MALHOTRA, NAGESHWAR HETEROCYCLIC AROMATICITY. HETEROCYCLES 1991, 32(1), PG 127 61. A REVIEW.a
  155891. GABRIEL WEATHERHEAD
  155892. 8015N
  155893. 2/28/96V
  155894. PEET, NORTON P.; LETOURNEAU, MICHAEL E. SYNTHESIS OF ANGULAR BENZODIPYRAZOLES AND RELATED SYSTEMS. HETEROCYCLES 1991, 32(1) PG 41 72. A REVIEW.a
  155895. GABRIEL WEATHERHEAD
  155896. 8016N
  155897. 2/28/96VmROBERTS, STANLEY M. SUGAR MIMICS
  155898. POTENTIAL ANTI INFECTIVES  CHEM IN BRITAIN 1991, 27(6), PG 518 20. A REVIEW.a
  155899. GABRIEL WEATHERHEAD
  155900. 8017N
  155901. 2/28/96V
  155902. JASPERSE, CRAIG P.; CURRAN, DENNIS P.; FEVIG, THOMAS RADICAL REACTIONS IN NATURAL PRODUCT SYNTHESIS. CHEM REV 1991, 91(6) PG 1237 86. A REVIEW.a
  155903. GABRIEL WEATHERHEAD
  155904. 8018N
  155905. 2/28/96
  155906. VnKROTO, H. W.; ALLAF, A. W.; BALM, S. P. C60: BUCKMINSTERFULLERENE. CHEM REV 1991, 91(6), PG 1213 35. A REVIEW.a
  155907. GABRIEL WEATHERHEAD
  155908. 8019N
  155909. 2/28/96V
  155910. BURGESS, KEVIN; OHLMEYER, MICHAEL J. TRANSITION METAL PROMOTED HYDROBORATIONS OF ALKENES, EMERGING METHODOLOGY FOR ORGANIC TRANSFORMATIONS. CHEM REV 1991, 91(6), PG 1179 91. A REVIEW.a
  155911. GABRIEL WEATHERHEAD
  155912. 8020N
  155913. 2/28/96VwELLER, KARSTEN; SCHWARZ, HELMUT. ORGANOMETALLIC CHEMISTRY IN THE GAS PHASE. CHEM REV 1991, 91(6), PG 1121 77. A REVIEW.a
  155914. GABRIEL WEATHERHEAD
  155915. 8021N
  155916. 2/28/96V~BADER, RICHARD F. W. A QUANTUM THEORY OF MOLECULAR STRUCTURE AND ITS APPLICATIONS. CHEM REV 1991, 91(5), PG 893 928. A REVIEW.a
  155917. GABRIEL WEATHERHEAD
  155918. 8022N
  155919. 2/28/96V
  155920. ORLANDI, GIORGIO; ZERBETTO, FRANCESCO; ZGIERSKI, MAREK Z. THEORETICAL ANALYSIS OF SPECTRA OF SHORT POLYENES. CHEM REV 1991 91(5), PG 867 91. A REVIEW.a
  155921. GABRIEL WEATHERHEAD
  155922. 8023N
  155923. 2/28/96
  155924. NEWTON, MARSHALL D. QUANTUM CHEMICAL PROBES OF ELECTRON TRANSFER KINETICS: THE NATURE OF DONOR ACCEPTOR INTERACTIONS. CHEM REV 1991, 91(5), PG 767 92. A REVIEW.a
  155925. GABRIEL WEATHERHEAD
  155926. 8024N
  155927. 2/28/96V
  155928. VEILLARD, ALAIN. AB INITIO CALCULATIONS OF TRANSITION METAL ORGANOMETALLICS: STRUCTURE AND MOLECULAR PROPERTIES. CHEM REV 1991 91(5),PG 743 66. A REVIEW.a
  155929. GABRIEL WEATHERHEAD
  155930. 8025N
  155931. 2/28/96V
  155932. NICOLAOU, K. C.; RAMPHAL, J. Y.; PETASIS, N. A.; SERHAN C. N. LIPOXINS AND RELATED EICOSANOIDS: BIOSYNTHESIS, BIOLOGICAL PROPERTIES, AND CHEMICAL SYNTHESIS. ANG CHEM INT ENG 1991, 30(9), PG 1100 16. A REVIEW.a
  155933. GABRIEL WEATHERHEAD
  155934. 8026N
  155935. 2/28/96VwMENGER, F. M. GROUPS OF ORGANIC MOLECULES THAT OPERATE COLLECTIVELY. ANG CHEM INT ENG 1991, 30(9),PG 1086 99. A REVIEW.a
  155936. GABRIEL WEATHERHEAD
  155937. 8027N
  155938. 2/28/96
  155939. RYABOV, ALEXANDER D. THE BIOCHEMICAL REACTIONS OF ORGANOMETALLICS WITH ENZYMES. ANG CHEM INT ENG 1991, 30(8), PG 931 941. A REVIEW.a
  155940. GABRIEL WEATHERHEAD
  155941. 8028N
  155942. 2/28/96V
  155943. RUCHARDT, CHRISTOPH; MEIER, MICHAEL; HAAF, KLAUS; PAKUSCH, JOACHIM, WOLBER, ERWIN K. A., MULLER, BARBARA. THE ISOCYANIDE CYANIDE REARRANGEMENT; MECHANISM AND PREPARATIVE APPLICATIONS. ANG CHEM INT ENG 1991, 30(8), PG 893 901. A REVIEW.a
  155944. GABRIEL WEATHERHEAD
  155945. 8029N
  155946. 2/28/96V|EUGSTER, CONRAD H.; MARKI FISCHER, EDITH. THE CHEMISTRY OF ROSE PIGMENTS. ANG CHEM INT ENG 1991, 30(6), PG 654 72. A REVIEW.a
  155947. GABRIEL WEATHERHEAD
  155948. 8030N
  155949. 2/28/96V
  155950. ENGLISCH, UWE; GAUSS, DIETER H. CHEMICALLY MODIFIED OLIGONUCLEOTIDES AS PROBES AND INHIBITORS. ANG CHEM INT ENG 1991, 30(6) PG 612 29. A REVIEW.a
  155951. GABRIEL WEATHERHEAD
  155952. 8031N
  155953. 2/28/96VpCARUTHERS, MARVIN H. CHEMICAL SYNTHESIS OF DNA AND DNA ANALOGS. ACCTS CHEM RES 1991, 24(9), PG 278 84. A REVIEW.
  155954. GABRIEL WEATHERHEAD
  155955. 8032N
  155956. 2/28/96VYBLEEKE, JOHN R. METALLABENZENE CHEMISTRY. ACCTS CHEM RES 1991, 24(9), PG 271 7. A REVIEW.a
  155957. GABRIEL WEATHERHEAD
  155958. 8033N
  155959. 2/28/96V}LUH, TIEN YAU. NEW SYNTHETIC APPLICATIONS OF THE DITHIOACETAL FUNCTIONALITY. ACCTS CHEM RES 1991, 24(9), PG 257 63. A REVIEW.a
  155960. GABRIEL WEATHERHEAD
  155961. 8034N
  155962. 2/28/96V
  155963. WALLING, CHEVES. THE NATURE OF RADICALS INVOLVED IN GRIGNARD REAGENT FORMATION. ACCTS CHEM RES 1991, 24(9), PG 255 6. A REVIEW.a
  155964. GABRIEL WEATHERHEAD
  155965. 8035N
  155966. 2/28/96V
  155967. THOMAS, ERIC J. CYTOCHALASAN SYNTHESIS: MACROCYCLE FORMATION VIA INTRAMOLECULAR DIELS ALDER REACTIONS. ACCTS CHEM RES 1991 24(8), PG 229 35. A REVIEW.a
  155968. GABRIEL WEATHERHEAD
  155969. 8036N
  155970. 2/28/96
  155971. BERSON, JEROME A. THE OVERLAP COMPONENT OF THE STEREOELECTRONIC FACTOR. REMOTE CONTROL OF STEREOGENICITY TRANSFER THROUGH THE ANISOTROPIC INFLUENCE OF A RING. ACCTS CHEM RES 1991, 24(7), PG 215 22. A REVIEW.a
  155972. GABRIEL WEATHERHEAD
  155973. 8037N
  155974. 2/28/96V
  155975. OAE, SHIGERU; UCHIDA, YUZURU. LIGAND COUPLING REACTIONS OF HYPERVALENT SPECIES. ACCTS CHEM RES 1991, 24(7), PG 202 8. A REVIEW.a
  155976. GABRIEL WEATHERHEAD
  155977. TETRAHEDRONC
  155978. BERSON JA REVIEWM
  155979. 8038N
  155980. 2/28/96VTDISCOVERIES MISSED, DISCOVERIES MADE   CREATIVITY, INFLUENCE, AND FAME IN CHEMISTRY.W
  155981. 1992 JAN 3X
  155982. 3 17Y
  155983. 48(1)a
  155984. GABRIEL WEATHERHEAD
  155985. TETRAHEDRONCGKATRITZKY SYNTHON SYNTHESIS REVIEW AMINE NITROGEN AUXILIARY HETEROCYCLEM
  155986. 8039N
  155987. 2/28/96V+BENZOTRIAZOLE:  A NOVEL SYNTHETIC AUXILIARYW
  155988. VOL 47 P 2683 1991a
  155989. GABRIEL WEATHERHEAD
  155990. TETRAHEDRONCQSTANOVNIK DIPOLAR CYCLOADDITION REVIEW NITROGEN HETEROCYCLE SYNTHESIS DIAZOALKANEM
  155991. 8040N
  155992. 2/28/96
  155993. V\1,3 DIPOLAR CYCLOADDITION OF DIAZOALKANES TO SOME NITROGEN CONTAINING HETEROAROMATIC SYSTEMSW
  155994. VOL 47 P 2925 1991a
  155995. GABRIEL WEATHERHEAD
  155996. TETRAHEDRONC,BEGUE FLUORINE REVIEW SYNTHESIS FLUORINATIONM
  155997. 8041N
  155998. 2/28/96V"PREPARATION OF FLUORINATED KETONESW
  155999. VOL 47 P 3207 1991a
  156000. GABRIEL WEATHERHEAD
  156001. TET LETTCQASYMMETRIC EPOXIDATION EPOSIDE METAL NICKEL SALEN REVIEW CHIRAL INDUCTION KATSUKIM
  156002. 8042N
  156003. 2/28/96V@CATALYTIC EPOXIDATION WITH MOLECULAR OXYGEN USING NICKEL COMPLEXW
  156004. P 6891 1991a
  156005. GABRIEL WEATHERHEAD
  156006. TET LETTCCMITSUNOBA PHOSPHOROUS CARBON DISPLACEMENT SUBSTITUTION REVIEW MACORM
  156007. 8043N
  156008. 2/28/96VWUSE OF O NITRO ARYL ACETONITRILES AS CARBON ACID PARTICIPANTS IN THE MITSUNOBU REACTIONW
  156009. P 7195 1991a
  156010. GABRIEL WEATHERHEAD
  156011. J ORG CHEMC}OLEFIN ALKENE REAGENT IODONIUM AZIRIDINE REVIEW CHIRAL METAL COPPER CATALYST AZIRIDINATION INDUCTION ENANTIOSELECTIVITY EVANSM
  156012. 8044N
  156013. 2/28/96
  156014. VTCOPPER CATALYZED AZIRIDINATION OF OLEFINS BY P TOLUENESULFONYL IMINO PHENYL IODINANEW
  156015. VOL 56 P 6744 1991a
  156016. GABRIEL WEATHERHEAD
  156017. SYNLETTCYEPOXIDE TITANIUM RING OPENING AZIDE REVIEW LEWIS ACID ORGANOMETALLIC METAL CATALYST OGUNIM
  156018. 8045N
  156019. 2/28/96V\ASYMMETRIC RING OPENING OF EPOXIDE WITH TRIMETHYLSILYL AZIDE USING CHIRAL TITANIUM COMPLEXESW
  156020. P 774 1991a
  156021. GABRIEL WEATHERHEAD
  156022. SYNLETTC[OLEFIN SILICON ALKENE PETERSON ALKOXIDE REVIEW STEREOCHEM SILYL ELIMINATION ALCOHOL BARRETTM
  156023. 8046N
  156024. 2/28/96V3RECENT STUDIES OF THE PETERSON OLEFINATION REACTIONW
  156025. P 764 1991a
  156026. GABRIEL WEATHERHEAD
  156027. 8047N
  156028. 2/28/96V
  156029. ZALEWSLI, ROMUALD I., KRYGOWSKI, TADEUSZ M., SHORTER JOHN, EDS. SIMILARITY MODELS IN ORGANIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY, 42). ELSEVIER: AMSTERDAM, 1991.  REVIEWa
  156030. GABRIEL WEATHERHEAD
  156031. 8048N
  156032. 2/28/96
  156033. WOLFE, J. F.; OGLIARUSO, M. A. SYNTHESIS OF CARBOXYLIC ACIDS, ESTERS AND THEIR DERIVATIVES (UPDATES TO THE CHEM  ISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1991.  REVIEWa
  156034. GABRIEL WEATHERHEAD
  156035. 8049N
  156036. 2/28/96V]VOGTLE, F. SUPRAMOLECULAR CHEMISTRY. AN INTRODUCTION.  WILEY: CHICHESTER, U.K., 1991.  REVIEWa
  156037. GABRIEL WEATHERHEAD
  156038. 8050N
  156039. 2/28/96VjTURRO, NICHOLAS. MODERN MOLECULAR PHOTOCHEMISTRY. UNIVERSITY SCIENCE BOOKS: MILL VALLEY, CA, 1991.  REVIEWa
  156040. GABRIEL WEATHERHEAD
  156041. 8051N
  156042. 2/28/96VfSINHA, S. S. REGIOSELECTIVE CATALYSTS. SINHA TECHNICAL SERVICES: DOMBIVLI (EAST), INDIA, 1990.  REVIEWa
  156043. GABRIEL WEATHERHEAD
  156044. 8052N
  156045. 2/28/96VISHONO TATSUYA. ELECTROORGANIC SYNTHESIS. ACADEMIC:  LONDON, 1991.  REVIEWa
  156046. GABRIEL WEATHERHEAD
  156047. 8053N
  156048. 2/28/96
  156049. SEAMAN, F.; BOHLMANN, F.; ZDERO, C.; MABRY, T. J.  DITERPENOIDS OF FLOWERING PLANTS. COMPOSITAE (ASTERACEAE). SPRINGER VERLAG: NEW YORK, 1990.  REVIEWa
  156050. GABRIEL WEATHERHEAD
  156051. 8054N
  156052. 2/28/96V
  156053. RUBIRALTA, MARIO; GIRALT, ERNEST, DIEZ, A. PIPERIDINE. STRUCTURE, PREPARATION, REACTIVITY AND SYNTHETIC APPLICA  TIONS OF PIPERIDINE AND ITS DERIVATIVES. (STUDIES IN ORGANIC CHEMISTRY, 43). ELSEVIER: AMSTERDAM, 1991.  REVIEWa
  156054. GABRIEL WEATHERHEAD
  156055. 8055N
  156056. 2/28/96V
  156057. ROOD, DEAN. A PRACTICAL GUIDE TO THE CARE,  MAINTENANCE, AND TROUBLESHOOTING OF CAPILLARY GAS CHROMATO  GRAPHIC SYSTEMS. HUTHIG: HEIDELBERG, FRG, 1991.  REVIEWa
  156058. GABRIEL WEATHERHEAD
  156059. 8056N
  156060. 2/28/96V
  156061. ROBERTS, JOHN D. THE RIGHT PLACE AT THE RIGHT TIME (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EM  INENT CHEMISTS). AMERICAN CHEMICAL SOCIETY WASHINGTON, DC, 1990.  REVIEWa
  156062. GABRIEL WEATHERHEAD
  156063. 8057N
  156064. 2/28/96
  156065. V;RIZK, ABDEL FATTAH M., ED. NATURALLY OCCURRING PYR   REVIEWa
  156066. GABRIEL WEATHERHEAD
  156067. 8058N
  156068. 2/28/96V
  156069. RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 8: STEREOSELECTIVE SYNTHESIS, PART E. ELSEVIER: AMSTERDAM, 1991.  REVIEWa
  156070. GABRIEL WEATHERHEAD
  156071. 8059N
  156072. 2/28/96V
  156073. RAHMAN, ATTA UR. HANDBOOK OF NATURAL PRODUCTS DATA, VOL. 1: DITERPENOID AND STEROIDAL ALKALOIDS. ELSEVIER: AMSTERDAM, 1990.  REVIEWa
  156074. GABRIEL WEATHERHEAD
  156075. 8060N
  156076. 2/28/96V
  156077. PRELOG, VLADIMIR. MY 128 SEMESTERS OF STUDIES OF CHEMISTRY. (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY WASHINGTON, DC, 1990.  REVIEWa
  156078. GABRIEL WEATHERHEAD
  156079. 8061N
  156080. 2/28/96V|PELLETIER, S. WILLIAM, ED. ALKALOIDS: CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 7. SPRINGER VERLAG: NEW YORK, 1991.  REVIEWa
  156081. GABRIEL WEATHERHEAD
  156082. 8062N
  156083. 2/28/96
  156084. PATAI, SAUL; RAPPOPORT, ZVI, EDS. THE CHEMISTRY OF SULFONIC ACIDS ESTERS, AND THEIR DERIVATIVES (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1991.  REVIEWa
  156085. GABRIEL WEATHERHEAD
  156086. 8063N
  156087. 2/28/96V
  156088. NAKANISHI, KOJI, ED. ONE DIMENSIONAL AND TWO DIMENSIONAL NMR SPECTRA BY MODERN PULSE TECHNIQUES. UNIVERSITY SCIENCE BOOKS: MILL VALLEY, CA, 1991.  REVIEWa
  156089. GABRIEL WEATHERHEAD
  156090. 8064N
  156091. 2/28/96V
  156092. METANOMSKI, W. V. COMPENDIUM OF MACROMOLECULAR NOMENCLATURE (INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY, MACROMOLECULAR DIVISION, COMMISSION ON MACROMOLECULAR NOMENCLATURE). BLACKWELL SCIENTIFIC PUBLICATIONS: LONDON, U.K., 1991.  REVIEWa
  156093. GABRIEL WEATHERHEAD
  156094. 8065N
  156095. 2/28/96VnMATSUMOTO, KIYOSHI; ACHESON, R MORRIN, EDS. ORGANIC SYNTHESIS AT HIGH PRESSURES. WILEY: NEW YORK 1991.  REVIEWa
  156096. GABRIEL WEATHERHEAD
  156097. 8066N
  156098. 2/28/96
  156099. MASON, T. J., ED. SONOCHEMISTRY: THE USES OF ULTRASOUND IN CHEMISTRY. ROYAL SOCIETY OF CHEMISTRY: CAMBRIDGE, U.K., 1990.  REVIEWa
  156100. GABRIEL WEATHERHEAD
  156101. 8067N
  156102. 2/28/96V
  156103. LOENING, K., MERRITT, J.; LATER, D.; WRIGHT, W. POLYNUCLEAR AROMATIC HYDROCARBONS. NOMENCLATURE GUIDE. 1ST ED. BATTELLE PRESS: COLUMBUS, OH, 1990.  REVIEWa
  156104. GABRIEL WEATHERHEAD
  156105. 8068N
  156106. 2/28/96V
  156107. LINGEMAN, H.; UNDERBERG, W. J. M., EDS. DETECTION ORIENTED DERIVATIZATION TECHNIQUES IN LIQUID CHROMATOGRAPHY. DEKKER: NEW YORK, 1990.  REVIEWa
  156108. GABRIEL WEATHERHEAD
  156109. 8069N
  156110. 2/28/96VMKEMP, WILLIAM. ORGANIC SPECTROSCOPY. 3RD ED. FREEMAN: NEW YORK, 1991.  REVIEWa
  156111. GABRIEL WEATHERHEAD
  156112. 8070N
  156113. 2/28/96V
  156114. HARTLEY, FRANK R., ED. THE CHEMISTRY OF ORGANOPHOSPHORUS COMPOUNDS, VOL. 1 (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1990.  REVIEWa
  156115. GABRIEL WEATHERHEAD
  156116. 8071N
  156117. 2/28/96
  156118. VaHANSEN, LEE D., ED. ORGANIC CHEMISTRY OF THE ATMOSPHERE. CRC PRESS: BOCA RATON, FL, 1991.  REVIEWa
  156119. GABRIEL WEATHERHEAD
  156120. 8072N
  156121. 2/28/96V
  156122. GRONOWITZ, SALO, ED. THIOPHENE AND ITS DERIVATIVES, PT. 4 (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 44, PT. 4). WILEY; NEW YORK, 1991.  REVIEWa
  156123. GABRIEL WEATHERHEAD
  156124. 8073N
  156125. 2/28/96V
  156126. GRANT, DAVID J. W., HIGUCHI, TAKERU. SOLUBILITY BEHAVIOR OF ORGANIC COMPOUMDS (TECHNIQUES OF CHEMISTRY, VOL. 21). WILEY: NEW YORK, 1990.  REVIEWa
  156127. GABRIEL WEATHERHEAD
  156128. 8074N
  156129. 2/28/96V
  156130. CRAM, DONALD J. FROM DISCOVERY TO DESIGN IN ORGANIC CHEMISTRY. (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY WASHINGTON, DC, 1990  REVIEWa
  156131. GABRIEL WEATHERHEAD
  156132. 8075N
  156133. 2/28/96V
  156134. ELIEL, ERNEST L. FROM COLOGNE TO CHAPEL HILL (PROFLLES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1990.  REVIEW
  156135. GABRIEL WEATHERHEAD
  156136. 8076N
  156137. 2/28/96V
  156138. DJERASSI, CARL. STEROIDS MADE IT POSSIBLE (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1990.  REVIEWa
  156139. GABRIEL WEATHERHEAD
  156140. 8077N
  156141. 2/28/96V^DIEDERICH, FRANCOIS N. CYCLOPHANES. ROYAL SOCIETY OF CHEMISTRY: CAMBRIDGE, U.K., 1991.  REVIEWa
  156142. GABRIEL WEATHERHEAD
  156143. 8078N
  156144. 2/28/96V
  156145. CYVIN, S. J.; BRUNVOLL, J.; CYVIN, B. N. THEORY OF CORONOID HYDROCARBONS (LECTURE NOTES IN CHEMISTRY, VOL. 54). SPRINGER VERLAG: BERLIN, 1991.  REVIEWa
  156146. GABRIEL WEATHERHEAD
  156147. 8079N
  156148. 2/28/96VoBRANDSMA, L., ET AL. PREPARATIVE POLAR ORGANOMETALLIC CHEMISTRY, VOL. 2. SPRINGER VERLAG: BERLIN, 1990.  REVIEWa
  156149. GABRIEL WEATHERHEAD
  156150. 8080N
  156151. 2/28/96ViBOYKIN, DAVID W., ED. 17O NMR SPECTROSCOPY IN ORGANIC CHEMISTRY. CRC PRESS: BOCA RATON, FL, 1991.  REVIEWa
  156152. GABRIEL WEATHERHEAD
  156153. 2/28/96ViBLACKBURN, G. MICHAEL, ED. NUCLEIC ACIDS IN CHEMISTRY AND BIOLOGY. IRL PRESS. OXFORD, U.K., 1990.  REVIEWa
  156154. GABRIEL WEATHERHEAD
  156155. 8082N
  156156. 2/28/96V
  156157. BERNAL, IVAN, ED. STEREOCHEMISTRY OF ORGANOMETALLIC AND INORGANIC COMPOUNDS, VOL. 4,  STEREOCHEMICAL CONTROL, BONDING, AND STERIC REARRANGEMENTS. ELSEVIER: AMSTERDAM 1990.  REVIEWa
  156158. GABRIEL WEATHERHEAD
  156159. 8083N
  156160. 2/28/96VYBAILEY P. D. AN INTRODUCTION TO PEPTIDE CHEMISTRY. WILEY: CHICHESTER, U.K., 1990.  REVIEWa
  156161. GABRIEL WEATHERHEAD
  156162. 8084N
  156163. 2/28/96VyATHERTON, E., SHEPPARD, R. C. SOLID PHASE PEPTIDE SYNTHESIS: A PRACTICAL APPROACH. IRL PRESS: OXFORD, U.K., 1989.  REVIEWa
  156164. GABRIEL WEATHERHEAD
  156165. 8085N
  156166. 2/28/96
  156167. AITKEN, R. ALAN, ARMSTRONG, DAVID P.; MESHER, SHAUN T. E. OXIDATION OF FIVE MEMBERED RING HETEROCYCLES CONTAINING N AND S.  PROGRESS IN HETEROCYCLIC CHEMISTRY. VOLUME 2, H. SUSCHITZKY AND E. F. V. SCRIVEN, EDS., PERGAMON PRESS, OXFORD, U.K., 1990.  REVIEWa
  156168. GABRIEL WEATHERHEAD
  156169. 8086N
  156170. 2/28/96V
  156171. MEIER, HERBERT. CYCLIC ALKYNES, ENYNES AND DIENYNES: A SYNTHETIC CHALLENGE.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156172. GABRIEL WEATHERHEAD
  156173. 8087N
  156174. 2/28/96V
  156175. LEE RUFF, ED. NEW SYNTHETIC PATHWAYS FROM CYCLOBUTANONES.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156176. GABRIEL WEATHERHEAD
  156177. 8088N
  156178. 2/28/96
  156179. PADWA, ALBERT; FRYXELL, GLEN E. CYCLIZATION AND CYCLOADDITION REACTIONS OF CYCLOPROPENES.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156180. GABRIEL WEATHERHEAD
  156181. 8089N
  156182. 2/28/96V
  156183. BAIRD, MARK S. 1 HALO  AND 1,2 DIHALOCYCLOPROPENES IN CHEMICAL SYNTHESIS.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156184. GABRIEL WEATHERHEAD
  156185. 8090N
  156186. 2/28/96V
  156187. BANWELL, MARTIN G.; REUM, MONICA E. GEM DIHALOCYCLOPROPANES IN CHEMICAL SYNTHESIS.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156188. GABRIEL WEATHERHEAD
  156189. 8091N
  156190. 2/28/96V
  156191. HALTON, BRIAN. PREFACE. STRAIN IN ORGANIC CHEMISTRY: A PERSPECTIVE.  ADVANCES IN STRAIN IN ORGANIC CHEMISTRY, VOLUME 1, BRIAN HALTON, ED., JAI PRESS, INC. GREENWICH, CT, 1991.  REVIEWa
  156192. GABRIEL WEATHERHEAD
  156193. 8092N
  156194. 2/28/96V
  156195. GUPTA, ASHOK K.; FU, XIAOYONG, SNYDER, JAMES P.; COOK, JAMES M. GENERAL APPROACH FOR THE SYNTHESIS OF POLYQUINENES VIA THE WEISS REACTION. 1991, 47(23), 3665 710. TETRAHEDRON  REVIEWa
  156196. GABRIEL WEATHERHEAD
  156197. 8093N
  156198. 2/28/96V
  156199. BEGUE, JEAN PIERRE; BONNET DELPON, DANIELE. PREPARATION OF TRIFLUOROMETHYL KETONES AND RELATED FLUORINATED KETONES. 1991, 47(20 21), 3207 58. TETRAHEDRON  REVIEWa
  156200. GABRIEL WEATHERHEAD
  156201. 8094N
  156202. 2/28/96V
  156203. STANOVNIK, BRANKO. 1,3 DIPOLAR CYCLOADDITIONS OF DIAZOALKANES TO SOME NITROGEN CONTAINING HETEROAROMATIC SYSTEMS. 1991, 47(18 19), 2925 45. TETRAHEDRON  REVIEWa
  156204. GABRIEL WEATHERHEAD
  156205. 8095N
  156206. 2/28/96V
  156207. KATRITZKY, ALAN R.; RACHWAL, STANISLAW HITCHINGS, GREGORY J. BENZOTRIAZOLE: A NOVEL SYNTHETIC AUXIHARY. 1991, 47(16 17), 2683 732. TETRAHEDRON  REVIEWa
  156208. GABRIEL WEATHERHEAD
  156209. 8096N
  156210. 2/28/96
  156211. SCHREIBER, STUART L., VERDINE, GREGORY L. PROTEIN OVERPRODUCTION FOR ORGANIC CHEMISTS. 1991, 47(14 15), 2543 62. TETRAHEDRON  REVIEWa
  156212. GABRIEL WEATHERHEAD
  156213. 8097N
  156214. 2/28/96V
  156215. ADAMS, JULIAN; SPERO, DENICE M. RHODIUM(II) CATALYZED REACTIONS OF DIAZO CARBONYL COMPOUNDS. 1991, 47(10 11), 1765 808. TETRAHEDRON  REVIEWa
  156216. GABRIEL WEATHERHEAD
  156217. 8098N
  156218. 2/28/96V
  156219. MATVEEV, YU. I.; GORBATENKO, V. I.; SAMARAI, L. I. 1,1 DIHALOALKYL HETEROCUMULENES: SYNTHESIS AND REACTIONS. 1991, 47(9), 1563 601. TETRAHEDRON  REVIEWa
  156220. GABRIEL WEATHERHEAD
  156221. 8099N
  156222. 2/28/96VzCLENNAN, EDWARD L. SYNTHETIC AND MECHANISTIC ASPECTS OF 1,3 DIENE PHOTOOXIDATION. 1991, 47(8),1343 82. TETRAHEDRON  REVIEWa
  156223. GABRIEL WEATHERHEAD
  156224. 8100N
  156225. 2/28/96V
  156226. HOFFMAN, ROBERT V. SYNTHETIC TRANSFORMATIONS USING ARENESULFONYLOXY GROUPS, FIRST AS ELECTROPHILES, THEN AS LEAVING GROUPS. 1991, 47(7), 1109 35. TETRAHEDRON  REVIEWa
  156227. GABRIEL WEATHERHEAD
  156228. 8101N
  156229. 2/28/96V
  156230. MUELLER WESTERHOFF, ULRICH T.; VANCE, BLAKE; YOON, DONG IHL. THE SYNTHESIS OF DITHIOLENE DYES WITH STRONG NEAR IR ABSORPTION. 1991, 47(6), 909 32. TETRAHEDRON  REVIEWa
  156231. GABRIEL WEATHERHEAD
  156232. 8102N
  156233. 2/28/96VuANDREAE, SIEGFRIED, SCHMITZ, ERNST. ELECTROPHILIC AMINATIONS WITH OXAZIRIDINES. 1991, (5), 327 341. SYNTHESIS  REVIEWa
  156234. GABRIEL WEATHERHEAD
  156235. 8103N
  156236. 2/28/96V
  156237. MARTIN, STEPHEN F.; GUINN, DENISE E. PRELOG DJERASSI LACTONIC ACID. A TARGET FOR DESIGN AND DEVELOPMENT OF STEREOSELECTIVE SYNTHETIC METHODS. 1991, (4), 245 262. SYNTHESIS  REVIEWa
  156238. GABRIEL WEATHERHEAD
  156239. 8104N
  156240. 2/28/96V
  156241. ZECCHI, GAETANO. 1,7 ELECTROCYCLIC REACTIONS OF ALPHA, BETA, GAMMA, DELTA UNSATURATED 1,3 DIPOLES AS A SYNTHETIC ROUTE TO SEVEN MEMBERED HETEROCYCLES. 1991, (3),181 188. SYNTHESIS  REVIEWa
  156242. GABRIEL WEATHERHEAD
  156243. 8105N
  156244. 2/28/96
  156245. -V~OISHI, TAKESHI; NAKATA, TADASHI. NEW ASPECTS OF STEREOSELECTIVE SYNTHESIS OF 1,3 POLYOLS. 1990, (B), 635 45. SYNTHESIS  REVIEWa
  156246. GABRIEL WEATHERHEAD
  156247. 8106N
  156248. 2/28/96V
  156249. SANTOYO GONZALEZ, FRANCISCO HERNANDEZ MATEO, FERNANDO. SYNTHESIS AND REACTIVITY OF SUGARS WITH TWO BRANCHES AT C 3. 1990, (12), 715. SYNLETT  REVIEWa
  156250. GABRIEL WEATHERHEAD
  156251. 8107N
  156252. 2/28/96V
  156253. ROESKY, HERBERT W. CHEMISTRY WITHOUT BORDERS BETWEEN MAIN GROUP AND TRANSITION ELEMENTS: METAL CONTAINING CYCLIC PHOSPHAZENES AND SILOXANES. 1990, (11), 651. SYNLETT  REVIEWa
  156254. GABRIEL WEATHERHEAD
  156255. 8108N
  156256. 2/28/96V
  156257. PIKE, R. D.; SWEIGART, D. A. SINGLE AND DOUBLE NUCLEOPHILIC ADDITION TO COORDINATED PI HYDROCARBONS: MANGANESE MEDIATED FUNCTIONALIZATION OF ARENES. 1990, (10), 564. SYNLETT  REVIEWa
  156258. GABRIEL WEATHERHEAD
  156259. 8109N
  156260. 2/28/96VtBHADURI, AMIYA P. KEY SYNTHETIC INTERMEDIATES FOR BIOLOGICALLY ACTIVE HETEROCYCLES. 1990, (10), 557. SYNLETT  REVIEW
  156261. GABRIEL WEATHERHEAD
  156262. 8110N
  156263. 2/28/96V
  156264. MCGOVERN, PATRICIA A., VOLLHARDT, K. PETER C. THE SYNTHESIS AND NOVEL REACTIVITY OF HOMO  AND HETERODINUCLEAR FULVALENE METAL CARBONYLS. 1990, (9), 493. SYNLETT  REVIEWa
  156265. GABRIEL WEATHERHEAD
  156266. 8111N
  156267. 2/28/96VcNOZAKI, HITOSI. THE ROLE OF METALS IN CARBENE SYNTHON INTRODUCTION. 1990, (8), 441. SYNLETT  REVIEWa
  156268. GABRIEL WEATHERHEAD
  156269. 8112N
  156270. 2/28/96V
  156271. HUDLICKY, TOMAS; SEOANE, GUSTAVO; PRICE, JOHN D.; GADAMASETTI KUMAR G. AN OVERVIEW OF THE TOTAL SYNTHESIS OF PYRROLIZIDINE ALKALOIDS VIA [4 + L] AZIDE DIENE ANNULATION METHODOLOGY. 1990, (8), 433. SYNLETT  REVIEWa
  156272. GABRIEL WEATHERHEAD
  156273. 8113N
  156274. 2/28/96V
  156275. MORIARTY, ROBERT M.; VAID, RADHE K.; KOSER, GERALD F. [HYDROXY(ORGANOSULFONYLOXY)IODO]ARENES IN ORGANIC SYNTHESIS. 1990, (7), 365. SYNLETT  REVIEWa
  156276. GABRIEL WEATHERHEAD
  156277. 8114N
  156278. 2/28/96
  156279. MORI, AKIRA; TAKESHITA, HITOSHI. ANODIC OXIDATION FOR THE SYNTHESES OF O  AND P TROPOQUINONE MONO  AND BISACETALS. 1990, (6), 301. SYNLETT  REVIEWa
  156280. GABRIEL WEATHERHEAD
  156281. 8115N
  156282. 2/28/96VjNAGATA, RYN; SAITO, ISAO. SELECTIVE OXIDATIONS BY PEROXIDE BASED REAGENTS. 1990, (6), 291. SYNLETT  REVIEWa
  156283. GABRIEL WEATHERHEAD
  156284. 8116N
  156285. 2/28/96V^ITO, YOSHIHIKO, MURAKAMI, MASAHIRO. METALATION OF ISOCYANIDES. 1990, (5), 245. SYNLETT  REVIEWa
  156286. GABRIEL WEATHERHEAD
  156287. 8117N
  156288. 2/28/96V
  156289. WIJESEKERA, TILAK P.; DOLPHIN, DAVID. 1 BROMO L9 METHYLBILADIENES AC; USEFUL PRECURSORS TO PORPHYRINS. 1990, (5) 235. SYNLETT  REVIEWa
  156290. GABRIEL WEATHERHEAD
  156291. 8118N
  156292. 2/28/96VxJUNG, MICHAEL E. SUBSTITUENT AND SOLVENT EFFECTS IN INTRAMOLECULAR DIELS ALDER REACTIONS. 1990, (4),186. SYNLETT  REVIEWa
  156293. GABRIEL WEATHERHEAD
  156294. 8119N
  156295. 2/28/96
  156296. BARLUENGA, J.; JOGLAR, J.; GONZALEZ, F. J.; FUSTERO, S. ELECTRONICALLY NEUTRAL 2 AZA 1,3 DIENES: ARE THEY USEFUL INTERMEDIATES IN ORGANIC SYNTHESIS? 1990, (3), 129. SYNLETT  REVIEWa
  156297. GABRIEL WEATHERHEAD
  156298. 8120N
  156299. 2/28/96V_LIPSHUTZ, BRUCE H. THE EVOLUTION OF HIGHER ORDER CYANOCUPRATES. 1990, (3), 119. SYNLETT  REVIEWa
  156300. GABRIEL WEATHERHEAD
  156301. 8121N
  156302. 2/28/96V
  156303. PIERS, WARREN E.; SHAPIRO, PAMELA J.; BUNEL, EMILIO E.; BERCAW, JOHN E. COPING WITH EXTREME LEWIS ACIDITY: STRATEGIES FOR THE SYNTHESIS OF STABLE, MONONUCLEAR ORGANOMETALLIC DERIVATIVES OF SCANDIUM. 1990, (2), 74. SYNLETT  REVIEWa
  156304. GABRIEL WEATHERHEAD
  156305. 8122N
  156306. 2/28/96V
  156307. PAQUETTE, LEO A. CARBONYL GROUP REGENERATION WITH SUBSTANTIVE ENHANCEMENT OF STRUCTURAL COMPLEXITY. 1990, (2), 67. SYNLETT  REVIEWa
  156308. GABRIEL WEATHERHEAD
  156309. 8123N
  156310. 2/28/96
  156311. DE MEIJERE, ARMIN; WESSJOHANN, LUDGER. TAILORING THE REACTIVITY OF SMALL RING BUILDING BLOCKS FOR ORGANIC SYNTHESIS. 1990, (1), 20. SYNLETT  REVIEWa
  156312. GABRIEL WEATHERHEAD
  156313. 8124N
  156314. 2/28/96V
  156315. PEARSON, ANTHONY J. MULTIPLE STEREOCONTROL USING ORGANOMETALLIC COMPLEXES. APPLICATIONS IN ORGANIC SYNTHESIS AND CONSIDERATION OF FUTURE PROSPECTS. 1990, (1),10. SYNLETT  REVIEWa
  156316. GABRIEL WEATHERHEAD
  156317. 8125N
  156318. 2/28/96V
  156319. OKAMURA, WILLIAM H.; CURTIN, MICHAEL L. PERICYCLIZATION OF VINYLALLENES IN ORGANIC SYNTHESIS: ON THE INTRAMOLECULAR DIELS ALDER REACTION. 1990, (1) 1. SYNLETT  REVIEWa
  156320. GABRIEL WEATHERHEAD
  156321. 8126N
  156322. 2/28/96V
  156323. BALDWIN, J. E.; ALDOUS, D. J.; CHAN, C., HARWOOD, L. M.; O'NEIL, I. A. PEACH, J. M. THE TOTAL SYNTHESIS OF ( ) ISONITRIN B (BEOXYTRICHOVIRIDIN). 1989, (1), 9. SYNLETT  REVIEWa
  156324. GABRIEL WEATHERHEAD
  156325. 8127N
  156326. 2/28/96
  156327. SAKURAI, HIDEKI. METAMORPHOSIS OF SYNTHETIC STRATEGIES WITH ALLYLIC SILANES: TETRACOORDINATED ALLYLIC SILANES INTO PENTACOORDINATED ALLYLIC SILICATES. 1989, (1),1. SYNLETT  REVIEWa
  156328. GABRIEL WEATHERHEAD
  156329. 8128N
  156330. 2/28/96V
  156331. FRANEK, WALTER. 1,2,4,5 TETRATHIANES. II. STRUCTURE AND SPECTROSCOPIC PROPERTIES, ELECTROCHEMISTRY, AROMA RESEARCH AND USES. 1991,10(3), 233 78. SULFUR REPORTS  REVIEWa
  156332. GABRIEL WEATHERHEAD
  156333. 8129N
  156334. 2/28/96VlFRANEK, WALTER. 1,2,4,5 TETRATHIANES. 1. SYNTHESES AND REACTIONS. 1991,10(3) 193 232. SULFUR REPORTS  REVIEWa
  156335. GABRIEL WEATHERHEAD
  156336. 8130N
  156337. 2/28/96V
  156338. WILLIAMS, CHARLES R.; HARPP, DAVID N. SULFUR EXTRUSION REACTIONS SCOPE AND MECHANISTIC ASPECTS. 1990, 10(2), 103 82. SULFUR REPORTS  REVIEWa
  156339. GABRIEL WEATHERHEAD
  156340. 8131N
  156341. 2/28/96
  156342. MINACHEV, KH. M.; DERGACHEV, A. A. AROMATIZATION OF LOW MOLECULAR WEIGHT PARAFFINS ON PENTASIL ZEOLITES. 1990, 59(9), 885 905.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156343. GABRIEL WEATHERHEAD
  156344. 8132N
  156345. 2/28/96V
  156346. SHILOV, A. E.; SHUL'PIN, G. B. ACTIVATION OF THE CARBON HYDROGEN BOND BY METAL COMPLEXES. 1990, 59(9), 853 867.  RUSSIAN  CHEMICAL REVIEWS   REVIEWa
  156347. GABRIEL WEATHERHEAD
  156348. 8133N
  156349. 2/28/96V|KUKUSHKIN, V. YU. DEOXYGENATION OF COORDINATED AND FREE SULFOXIDES. 1990, 59(9), 844 852.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156350. GABRIEL WEATHERHEAD
  156351. 8134N
  156352. 2/28/96V
  156353. PETROV, K. A.; RUDNEV, G. V.; SOROKIN, V. D. SULFENAMIDES AND THEIR DERIVATIVES. 1990, 59(9), 832 843.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156354. GABRIEL WEATHERHEAD
  156355. 8135N
  156356. 2/28/96VpKOVAL, I. V. PROGRESS IN THE CHEMISTRY OF SULFILIMINES. 1990, 59(9), 819 831.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156357. GABRIEL WEATHERHEAD
  156358. 8136N
  156359. 2/28/96
  156360. GUBNITSKAYA, E. S.; PERESYPKINA, L. P.; SAMARAI, L. I. BETA AMINOPHOSPHONATES AND BETA AMMOPHOSPHINATES, SYNTHESIS AND PROPERTIES. 1990, 59(8), 807 817.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156361. GABRIEL WEATHERHEAD
  156362. 8137N
  156363. 2/28/96V
  156364. VORONKOV, M. G.; DERYAGINA, E. N. THERMAL REACTIONS OF THIYL RADICALS. 1990, 59(8), 778 791.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156365. GABRIEL WEATHERHEAD
  156366. 8138N
  156367. 2/28/96V
  156368. ARTAMKINA, G. A.; KOVALENKO, S. V.; BELETSKAYA, I. P.; REUTOV, 0. A. CARBON CARBON BOND FORMATION IN ELECTRON DEFICIENT AROMATIC COMPOUNDS. 1990, 59(8), 750 777.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156369. GABRIEL WEATHERHEAD
  156370. 8139N
  156371. 2/28/96V
  156372. AKSE'NOV, V. V., VLASOV, V. M.; SHNITKO, G. N. INTERCALATION COMPOUNDS OF ALKALI METALS IN GRAPHITE IN FINE ORGANIC SYNTHESIS. 1990, 59(8), 738 749.  RUSSIAN  CHEMICAL REVIEWS  REVIEWa
  156373. GABRIEL WEATHERHEAD
  156374. 8140N
  156375. 2/28/96
  156376. BURSTEN, BRUCE E. SOME COMMENTS ON APPROXIMATE LCAO MOLECULAR ORBITAL THEORY IN ORGANOMETALLIC CHEMISTRY GETTING MORE BY DOING LESS? 1991, 63(6), 839 44. PURE AND APPLIED CHEMISTRY  REVIEWa
  156377. GABRIEL WEATHERHEAD
  156378. 8141N
  156379. 2/28/96V
  156380. BREGADZE, V. I.; KAMPEL, V. TS.; USYATINSKII, A. YA.GODOVIKOV, N. N. CARBORANYL DERIVATIVES OF NONTRANSITION METALS. 1991, 63(6), 835 8. PURE AND APPLIED CHEMISTRY  REVIEWa
  156381. GABRIEL WEATHERHEAD
  156382. 8142N
  156383. 2/28/96V
  156384. LEE, T. RANDALL; LAIBINIS, PAUL E.; FOLKERS, JOHN P. WHITESIDES, GEORGE M. HETEROGENEOUS CATALYSIS ON PLATINUM AND SELF ASSEMBLED MONOLAYERS ON METAL AND METAL OXIDE SURFACES. 1991, 63(6), 821 8. PURE AND APPLIED CHEMISTRY  REVIEWa
  156385. GABRIEL WEATHERHEAD
  156386. 8143N
  156387. 2/28/96V
  156388. SCHUMANN, HERBERT. MAIN GROUP METALLOCENES WITH SUBSTITUTED CYCLOPENTADIENYL LIGANDS: FROM BONDING PROBLEMS TO DISCOTIC PHASES. 1991, 63(6), 813 20. PURE AND APPLIED CHEMISTRY  REVIEWa
  156389. GABRIEL WEATHERHEAD
  156390. 8144N
  156391. 2/28/96V
  156392. ERKER, GERHARD. STEREOCHEMISTRY AND CATALYSIS WITH ZIRCONIUM COMPLEXES. 1991, 63(6), 797 806. PURE AND APPLIED CHEMISTRY  REVIEWa
  156393. GABRIEL WEATHERHEAD
  156394. 8145N
  156395. 2/28/96VqTAUBE, HENRY. ASPECTS OF ETA 2 BINDING BY OSMIUM AMMINES. 1991, 63(5), 651 64. PURE AND APPLIED CHEMISTRY  REVIEWa
  156396. GABRIEL WEATHERHEAD
  156397. 8146N
  156398. 2/28/96V
  156399. VAHRENKAMP, HEINRICH. LIGAND SPHERE REACTIVITY OF ORGANOMETALLIC CLUSTERS. L991, 63(5), 643 9. PURE AND APPLIED CHEMISTRY  REVIEWa
  156400. GABRIEL WEATHERHEAD
  156401. 8147N
  156402. 2/28/96V
  156403. NICOLAOU, K. C.; CAULFIELD, T. J.; GRONEBERG, R. D. SYNTHESIS OF NOVEL OLIGOSACCHARIDES. L991, 63(4), 555 60. PURE AND APPLIED CHEMISTRY  REVIEWa
  156404. GABRIEL WEATHERHEAD
  156405. 8148N
  156406. 2/28/96VrSINAY, PIERRE. RECENT ADVANCES IN GLYCOSYLATION REACTIONS. 1991, 63(4), 519 28. PURE AND APPLIED CHEMISTRY  REVIEWa
  156407. GABRIEL WEATHERHEAD
  156408. 8149N
  156409. 2/28/96
  156410. VASELLA, ANDREA. NEW REACTIONS AND INTERMEDIATES INVOLVING THE ANOMERIC CENTER. 1991, 63(4), 507 18. PURE AND APPLIED CHEMISTRY  REVIEWa
  156411. GABRIEL WEATHERHEAD
  156412. 8150N
  156413. 2/28/96V
  156414. YAMAMOTO, YOSHINORI. MOLECULAR DESIGN AND SYNTHESIS OF BORON 10 CARRIERS FOR NEUTRON CAPTURE THERAPY. 1991, 63(3), 423 6. PURE AND APPLIED CHEMISTRY  REVIEWa
  156415. GABRIEL WEATHERHEAD
  156416. 8151N
  156417. 2/28/96V{ENGLERT, GERHARD. NMR OF CAROTENOIDS: NOVEL EXPERIMENTAL TECHNIQUES. 1991, 63(1), 59 70. PURE AND APPLIED CHEMISTRY  REVIEWa
  156418. GABRIEL WEATHERHEAD
  156419. 8152N
  156420. 2/28/96VyPAUST, J. RECENT PROGRESS IN COMMERCIAL RETINOIDS AND CAROTENOIDS. 1991, 63(1), 45 58. PURE AND APPLIED CHEMISTRY  REVIEWa
  156421. GABRIEL WEATHERHEAD
  156422. 8153N
  156423. 2/28/96V
  156424. BERNHARD, KURT; MAYER, HANS. RECENT ADVANCES IN THE SYNTHESIS OF ACHIRAL CAROTENOIDS. 1991, 63(1), 35 44. PURE AND APPLIED CHEMISTRY  REVIEWa
  156425. GABRIEL WEATHERHEAD
  156426. 8154N
  156427. 2/28/96
  156428. ABAD, ANTONIO; AGULLO, CONSUELO; ARNO, MANUEL; DOMINGO, LUIS R.; ZARAGOZA, RAMON J. CONVERSION OF RESIN ACIDS INTO STEROIDAL COMPOUNDS. 1991, 23(3), 321 56. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  REVIEWa
  156429. GABRIEL WEATHERHEAD
  156430. 8155N
  156431. 2/28/96V
  156432. CLARAMUNT, ROSA MARIA; ELGUERO, JOSE. THE CHEMISTRY OF PYRAZOLIDINONES. 1991, 23(3), 273 320. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL  REVIEWa
  156433. GABRIEL WEATHERHEAD
  156434. 8156N
  156435. 2/28/96V
  156436. EFFENBERGER, FRANZ; WOLF, HANS CHRISTOPH. TERMINALLY SUBSTITUTED CONJUGATED POLYENES: SYNTHESIS AND ENERGY TRANSFER PROPERTIES. 1991,15(2 3),117 23. NEW JOURNAL OF CHEMISTRY  REVIEWa
  156437. GABRIEL WEATHERHEAD
  156438. 8157N
  156439. 2/28/96VjLIAAEN JENSEN S. MARINE CAROTENOIDS SELECTED TOPICS 1990, 14(10), 747 59. NEW JOURNAL OF CHEMISTRY  REVIEWa
  156440. GABRIEL WEATHERHEAD
  156441. 8158N
  156442. 2/28/96V^CHEN, BANG CHI. MELDRUM'S ACID IN ORGANIC SYNTHESIS. 1991, 32(3), 529 97. HETEROCYCLES  REVIEW
  156443. GABRIEL WEATHERHEAD
  156444. 8159N
  156445. 2/28/96V
  156446. CHANDRASEKHAR, VADAPALLI, MURALIDHARA, MADALIGAR GOPALAKRISHNA RAO; SELVARAJ, IYKKIAM IMMANUEL. REACTIONS OF CHLOROCYCLO PHOSPHAZENES WITH DIFUNCTIONAL REAGENTS. L990, 31(12), 2231 66.  HETEROCYCLES  REVIEWa
  156447. GABRIEL WEATHERHEAD
  156448. 8160N
  156449. 2/28/96VtNICOLAOU, K. C. CHEMICAL SYNTHESIS OF GLYCOSPHINGOLIPIDS. 1991, 4(3), 181 198. CHEMTRACTS: ORGANIC CHEMISTRY  REVIEWa
  156450. GABRIEL WEATHERHEAD
  156451. 8161N
  156452. 2/28/96V
  156453. JORGENSEN, WILLIAM L. COMPUTATIONAL INSIGHTS ON INTERMOLECULAR INTERACTIONS AND BINDING IN SOLUTION. 1991, 4(2), 91 119. CHEMTRACTS: ORGANIC CHEMISTRY  REVIEWa
  156454. GABRIEL WEATHERHEAD
  156455. 8162N
  156456. 2/28/96V
  156457. STANCOVIV, CHARLES J.; SCHREIBER, STUART, L. MOLECULAR DESIGN OF TRANSMEMBRANE ION CHANNELS. 1991, 4(1),1 20. CHEMTRACTS: ORGANIC CHEMISTRY  REVIEWa
  156458. GABRIEL WEATHERHEAD
  156459. 8163N
  156460. 2/28/96
  156461. NICOLAOU, K. C., OGILVIE, W. W. THE TOTAL SYNTHESIS OF AMPHOTERONOLIDE B AND AMPHOTERICIN B. 1990, 3(5), 327 349. CHEMTRACTS: ORGANIC CHEMISTRY  REVIEWa
  156462. GABRIEL WEATHERHEAD
  156463. 8164N
  156464. 2/28/96V
  156465. DAVIES, H. GEOFFREY;  GREEN, RICHARD H. AVERMECTINS AND MILBEMYCINS PART 1. 1991, 20(2), 211 269. CHEMICAL SOCIETY REVIEWS  REVIEWa
  156466. GABRIEL WEATHERHEAD
  156467. 8165N
  156468. 2/28/96V}RIDD, J. H. THE RANGE OF RADICAL PROCESSES IN NITRATION BY NITRIC ACID. 1991, 20(2),149 165. CHEMICAL SOCIETY REVIEWS  REVIEWa
  156469. GABRIEL WEATHERHEAD
  156470. 8166N
  156471. 2/28/96VyBARRETT, ANTHONY G. M. HETEROSUBSTITUTED NITROALKENES IN SYNTHESIS. 1991, 20(1), 95 127. CHEMICAL SOCIETY REVIEWS  REVIEWa
  156472. GABRIEL WEATHERHEAD
  156473. 8167N
  156474. 2/28/96V
  156475. MINGOS, D. MICHAEL P.; BAGHURST, DAVID R. APPLICATIONS OF MICROWAVE DIELECTRIC HEATING EFFECTS TO SYNTHETIC PROBLEMS IN CHEMISTRY. 1991, 20(1),1 47. CHEMICAL SOCIETY REVIEWS  REVIEWa
  156476. GABRIEL WEATHERHEAD
  156477. 8168N
  156478. 2/28/96V
  156479. CAMINADE, ANNE MARIE; MAJORAL, JEAN PIERRE; MATHIEU, RENE. SYNTHESIS OF DI , TRI , AND POLYPHOSPHANE AND PHOSPHENE TRANSITION METAL COMPLEXEX. 1991, 91(4), 575 612. CHEMICAL REVIEWS  REVIEWa
  156480. GABRIEL WEATHERHEAD
  156481. 8169N
  156482. 2/28/96V
  156483. DOHERTY, NANCY M.; HOFFMANN, NORRIS W. TRANSITION METAL FLUORO COMPOUNDS CONTAINING CARBONYL, PHOSPHINE, ARSINE, AND STIBINE LIGANDS. 1991, 91(4), 553 73. CHEMICAL REVIEWS  REVIEWa
  156484. GABRIEL WEATHERHEAD
  156485. 8170N
  156486. 2/28/96V
  156487. POLI, RINALDO. MONOCYCLOPENTADIENYL HALIDE COMPLEXES OF THE D  AND F BLOCK ELEMENTS. 1991, 91(4), 509 51. CHEMICAL REVIEWS  REVIEWa
  156488. GABRIEL WEATHERHEAD
  156489. 8171N
  156490. 2/28/96V
  156491. NDOU, THILIVHALI T; WARNER, ISIAH M. APPLICATIONS OF MULTIDIMENSIONAL ABSORPTION AND LUMINESCENCE SPECTROSCOPIES IN ANALYTICAL CHEMISTRY. 1991, 91(4), 493 507. CHEMICAL REVIEWS  REVIEWa
  156492. GABRIEL WEATHERHEAD
  156493. 8172N
  156494. 2/28/96
  156495. pVzLIPCZYNSKA, KOCHANY EWA. PHOTOCHEMISTRY OF HYDROXAMIC ACIDS AND DERIVATIVES. 1991, 91(4), 477 91. CHEMICAL REVIEWS  REVIEWa
  156496. GABRIEL WEATHERHEAD
  156497. 8173N
  156498. 2/28/96V
  156499. HANSON, ROBERT M. THE SYNTHETIC METHODOLOGY OF NONRACERNIC GLYCIDOL AND RELATED 2,3 EPOXY ALCOHOLS. 1991, 91(4), 437 76. CHEMICAL REVIEWS  REVIEWa
  156500. GABRIEL WEATHERHEAD
  156501. 8174N
  156502. 2/28/96VhWALDECK DAVID H. PHOTOISOMERIZATION DYNAMICS OF STILBENES. 1991, 91(3), 415 36. CHEMICAL REVIEWS  REVIEWa
  156503. GABRIEL WEATHERHEAD
  156504. 8175N
  156505. 2/28/96VoENGELKING, PAUL C. SPECTROSCOPY OF JET COOLED IONS AND RADICALS. 1991, 91(3), 399 414. CHEMICAL REVIEWS  REVIEWa
  156506. GABRIEL WEATHERHEAD
  156507. 8176N
  156508. 2/28/96VxSAUNDERS, MARTIN, JIMENEZ VAZQUEZ, HUGO A. RECENT STUDIES OF CARBOCATIONS. 1991, 91(3), 375 97. CHEMICAL REVIEWS  REVIEWa
  156509. GABRIEL WEATHERHEAD
  156510. 8177N
  156511. 2/28/96
  156512. WENTRUP CURT; KAMBOUNS, PETER. N SULFIDES. DINITROGEN SULFIDE, THIOFULMINIC ACID, AND NITRILE SULFIDES. 1991, 91(3), 363 73. CHEMICAL REVIEWS  REVIEWa
  156513. GABRIEL WEATHERHEAD
  156514. 8178N
  156515. 2/28/96V}BUNNELLE, WILLIAM H. PREPARATION, PROPERTIES, AND REACTIONS OF CARBONYL OXIDES. 1991, 91(3), 335 62. CHEMICAL REVIEWS  REVIEWa
  156516. GABRIEL WEATHERHEAD
  156517. 8179N
  156518. 2/28/96V]NEUMANN, WILHELM P. GERMYLENES AND STANNYLENES. 1991, 91(3), 311 34. CHEMICAL REVIEWS  REVIEWa
  156519. GABRIEL WEATHERHEAD
  156520. 8180N
  156521. 2/28/96V
  156522. PADWA, ALBERT; HORNBUCKLE, SUSAN F. YLIDE FORMATION FROM THE REACTION OF CARBENES AND CARBENOIDS WITH HETEROATOM LONE PAIRS. 1991, 91(3), 263 309. CHEMICAL REVIEWS  REVIEWa
  156523. GABRIEL WEATHERHEAD
  156524. 8181N
  156525. 2/28/96
  156526. BUSCHMANN, HELMUT; SCHARF, HANS DIETER; HOFFMANN, NORBERT; ESSER PETER. THE ISOINVERSION PRINCIPLE. A GENERAL MODEL OF CHEMICAL SELECTIVITY. 1991, 30(5), 477 515. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156527. GABRIEL WEATHERHEAD
  156528. 8182N
  156529. 2/28/96V
  156530. COREY, ELIAS JAMES. THE LOGIC OF CHEMICAL SYNTHESIS: MULTISTEP SYNTHESIS OF COMPLEX CARBOGENIC MOLECULES. (NOBEL LECTURE). 1991, 30(5), 455 65. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156531. GABRIEL WEATHERHEAD
  156532. 8183N
  156533. 2/28/96V
  156534. SEPPELT, KONRAD. FLUORINE STABILIZED SULFUR CARBON MULTIPLE BONDS. 1991, 30(4), 361 74. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156535. GABRIEL WEATHERHEAD
  156536. 8184N
  156537. 2/28/96V
  156538. HEIMGARTNER, HEINZ. 3 AMINO 2H AZIRINE. SYNTHONS FOR ALPHA, ALPHA DISUBSTITUTED ALPHA AMINO ACIDS IN HETEROCYCLE AND PEPTIDE SYNTHESIS. 1991, 30(3), 238 65  ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156539. GABRIEL WEATHERHEAD
  156540. 8185N
  156541. 2/28/96V
  156542. NIECKE, EDGAR; GUDAT, DIETRICH. IMINOPHOSPHINES: UNCONVENTIONAL COMPOUNDS OF MAIN GROUP ELEMENTS. 1991, 30(3), 217 37. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156543. GABRIEL WEATHERHEAD
  156544. 8186N
  156545. 2/28/96V
  156546. ZINSMEISTER, HANS DIETMAR;  BECKER, HANS; EICHER, THEOPHIL. BRYOPHITES, A SOURCE OF BIOLOGICALLY ACTIVE, NATURALLY OCCURRING MATERIAL. 1991, 30(2),130 47. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156547. GABRIEL WEATHERHEAD
  156548. 8187N
  156549. 2/28/96V
  156550. BAYER, ERNST. TOWARD THE CHEMICAL SYNTHESIS OF PROTEINS. 1991, 30(2), 113 29. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH  REVIEWa
  156551. GABRIEL WEATHERHEAD
  156552. 8188N
  156553. 2/28/96ViSODERQUIST JOHN A. SAMARIUM(II) IODIDE IN ORGANIC SYNTHESIS. 1991, 24(1),15 23. ALDRICHIMICA ACTA  REVIEWa
  156554. GABRIEL WEATHERHEAD
  156555. 8189N
  156556. 2/28/96
  156557. ALPER, HOWARD. SIMPLE, NOVEL METHODS FOR THE SYNTHESIS OF CARBONYL COMPOUNDS USING METAL COMPLEXES AS CATALYSTS. 1991, 24(1) 3 7. ALDRICHIMICA ACTA  REVIEWa
  156558. GABRIEL WEATHERHEAD
  156559. 8190N
  156560. 2/28/96VgGRAY, HARRY B. LONG RANGE ELECTRON TRANSFER IN PROTEINS. I990, 23(4), 87 93.  ALDRICHIMICA ACTA  REVIEWa
  156561. GABRIEL WEATHERHEAD
  156562. 8191N
  156563. 2/28/96V
  156564. BRESLOW, RONALD. HYDROPHOBIC EFFECTS ON SIMPLE ORGANIC REACTIONS IN WATER. 1991, 24(6),159 64.  ACCOUNTS OF CHEMICAL RESEARCH  REVIEWa
  156565. GABRIEL WEATHERHEAD
  156566. 8192N
  156567. 2/28/96V
  156568. RAJANBABU, T. V. STEREOCHEMISTRY OF INTRAMOLECULAR FREE RADICAL CYCLIZATION REACTIONS. 1991, 24(5),139 45.  ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  156569. GABRIEL WEATHERHEAD
  156570. 8193N
  156571. 2/28/96V
  156572. ZOLLINGER, H. COLOR CHEMISTRY.  SYNTHESES, PROPERTIES AND APPLICATIONS OF ORGANIC DYES AND PIGMENTS, 2ND ED. VCH: WEINHEIM, FRG, 1991. REVIEWa
  156573. GABRIEL WEATHERHEAD
  156574. 8194N
  156575. 2/28/96
  156576. VvWARD, DAVID J., ED. PEPTIDE PHARMACEUTICALS. APPROACHES TO THE DESIGN OF NOVEL DRUGS. ELSEVIER: NEW YORK, 1991. REVIEWa
  156577. GABRIEL WEATHERHEAD
  156578. 8195N
  156579. 2/28/96V
  156580. TOWNSEND, LEROY B.; TIPSON, R. STUART, EDS. NUCLEIC ACID CHEMISTRY, PT. 4. IMPROVED AND NEW SYNTHETIC PROCEDURES, METHODS, AND TECHNIQUES. WILEY: NEW YORK, 1991 REVIEWa
  156581. GABRIEL WEATHERHEAD
  156582. 8196N
  156583. 2/28/96VSSIMONYI, M., ED. CHIRAL MOLECULES. AKADEMIAI KIADO: BUDAPEST, HUNGARY, 1990. REVIEWa
  156584. GABRIEL WEATHERHEAD
  156585. 8197N
  156586. 2/28/96V
  156587. SHEPHERD, M. K. CYCLOBUTARENES. THE CHEMISTRY OF BENZOCYCLOBUTENE, BIPHENYLENE, AND RELATED COMPOUNDS. ELSEVIER: AMSTERDAM, 1991. REVIEWa
  156588. GABRIEL WEATHERHEAD
  156589. 8198N
  156590. 2/28/96VoRIZK, ABDEL FATTAH M., ED. NATURALLY OCCURRING PYRROLIZIDINE ALKALOIDS. CRC PRESS: BOCA RATON, FL, 1990. REVIEWa
  156591. GABRIEL WEATHERHEAD
  156592. 8199N
  156593. 2/28/96
  156594. RAHMAN, ATTA UR. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 7: STRUCTURE AND CHEMISTRY, PT. A. ELSEVIER: AMSTERDAM, 1989. REVIEWa
  156595. GABRIEL WEATHERHEAD
  156596. 8200N
  156597. 2/28/96ViOLAH, GEORGE A.; SQUIRE, DAVID R. CHEMISTRY OF ENERGETIC MATERIALS. ACADEMIC: SAN DIEGO, CA, 1991. REVIEWa
  156598. GABRIEL WEATHERHEAD
  156599. 8201N
  156600. 2/28/96V
  156601. NOZOE, TETSUO. SEVENTY YEARS IN ORGANIC CHEMISTRY (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON DC, 1990. REVIEWa
  156602. GABRIEL WEATHERHEAD
  156603. 8202N
  156604. 2/28/96V{NASIPURI, D. STEREOCHEMISTRY OF ORGANIC COMPOUNDS. PRINCIPLES NND APPLICATIONS. WILEY EASTERN LTD.: NEW DELHI, 1991. REVIEWa
  156605. GABRIEL WEATHERHEAD
  156606. 8203N
  156607. 2/28/96V
  156608. NAKANISHI, KOJI. A WANDERING NATURAL PRODUCTS CHEMIST (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1991. REVIEWa
  156609. GABRIEL WEATHERHEAD
  156610. 8204N
  156611. 2/28/96V
  156612. MINKIN, V. I., SIMKIN, B. YA.; MINAYAEV, R. M. QUANTUM CHEMISTRY OF ORGANIC COMPOUNDS MECHANISMS OF REACTIONS. SPRINGER VERLAG: HEIDELBERG, FRG, 1990. REVIEWa
  156613. GABRIEL WEATHERHEAD
  156614. 8205N
  156615. 2/28/96V
  156616. MCQUILLIN, F. J.; PARKER, D. G., STEPHENSON, G. R. TRANSITION METAL ORGANOMETALLICS FOR ORGANIC SYNTHESIS. CAMBRIDGE UNIVERSITY PRESS: NEW YORK, 1991. REVIEWa
  156617. GABRIEL WEATHERHEAD
  156618. 8206N
  156619. 2/28/96V
  156620. LIN VIEN, DAIMAY, COLTHUP, NORMAN B.; FATELEY, WILLIAM G.; GRASELLI, JEANETTE G. THE HANDBOOK OF INFRARED AND RAMAN CHARACTERISTIC FREQUENCIES OF ORGANIC MOLECULES. ACADEMIC: SAN DIEGO, CA, 1991. REVIEWa
  156621. GABRIEL WEATHERHEAD
  156622. 8207N
  156623. 2/28/96V
  156624. LEMIEUX, RAYMOND U. EXPLORATIONS WITH SUGARS: HOW SWEET IT WAS (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC 1990 REVIEWa
  156625. GABRIEL WEATHERHEAD
  156626. 8208N
  156627. 2/28/96
  156628. VXKALSI, P. S. STEREOCHEMISTRY: CONFORMATION AND MECHANISM. WILEY: NEW DELHI, 1990. REVIEWa
  156629. GABRIEL WEATHERHEAD
  156630. 8209N
  156631. 2/28/96VmJUARISTI, EUSEBIO. INTRODUCTION TO STEREOCHEMISTRY AND CONFORMATIONAL ANALYSIS. WILEY: NEW YORK, 1991. REVIEWa
  156632. GABRIEL WEATHERHEAD
  156633. 8210N
  156634. 2/28/96
  156635. JORK, HELLMUT; FUNK, WERNER;  FISCHER, WALTER; WIMMER, HANS. THIN LAYER CHROMATOGRAPHY: REAGENTS AND DETECTION METHODS, VOL. 1A: PHYSICAL AND CHEMICAL DETECTION METHODS: FUMDAMENTALS, REAGENTS 1 (TRANSLATED FROM THE GERMAN). VCH: WEINHEIM, FRG, 1990. REVIEW
  156636. GABRIEL WEATHERHEAD
  156637. 8211N
  156638. 2/28/96V\JONES, JOHN. THE CHEMICAL SYNTHESIS OF PEPTIDES. CLARENDON PRESS: OXFORD, U.K., 1991. REVIEWa
  156639. GABRIEL WEATHERHEAD
  156640. 8212N
  156641. 2/28/96VJHO, TSE LOK. POLARITY CONTROL FOR SYNTHESIS. WILEY: NEW YORK, 1991. REVIEWa
  156642. GABRIEL WEATHERHEAD
  156643. 8213N
  156644. 2/28/96
  156645. VWHESSE, MANFRED. RING ENLARGEMENT IN ORGANIC CHEMISTRY. VCH: WEINHEIM, FRG, 1991. REVIEWa
  156646. GABRIEL WEATHERHEAD
  156647. 8214N
  156648. 2/28/96V
  156649. HAVINGA, EGBERT. ENJOYING ORGANIC CHEMISTRY, 1927 1987 (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1991. REVIEWa
  156650. GABRIEL WEATHERHEAD
  156651. 8215N
  156652. 2/28/96VtGREENE, THEODORA W.; WUTS, PETER G. M. PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, 2ND ED. WILEY: NEW YORK, 1991. REVIEWa
  156653. GABRIEL WEATHERHEAD
  156654. 8216N
  156655. 2/28/96VfGOKEL, GEORGE W. CROWN ETHERS AND CRYPTANDS. ROYAL SOCIETY OF CHEMISTRY: CAMBRIDGE, U.K., 1991. REVIEWa
  156656. GABRIEL WEATHERHEAD
  156657. 8217N
  156658. 2/28/96V
  156659. GILBERT, ANDREW; BAGGOTT, JIM. ESSENTIALS OF MOLECULAR PHOTOCHEMISTRY. BLACKWELL SCIENTIFIC PUBLICATIONS: OXFORD U.K., 1991. REVIEWa
  156660. GABRIEL WEATHERHEAD
  156661. 8218N
  156662. 2/28/96
  156663. VlFUJITA, SHINSAKU. SYMMETRY AND COMBINATORIAL ENUMERATION IN CHEMISTRY. SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156664. GABRIEL WEATHERHEAD
  156665. 8219N
  156666. 2/28/96V
  156667. FRYER, R. IAN, ED. BICYCLIC DIAZEPINES. DIAZEPINES WITH AN ADDITIONAL RING (CHEMISTRY OF HETEROCYCLIC COMPOUNDS VOL. 50). WILEY: NEW YORK, 1991 . REVIEWa
  156668. GABRIEL WEATHERHEAD
  156669. 8220N
  156670. 2/28/96V
  156671. DEWAR, MICHAEL J. S. A SEMIEMPIRICAL LIFE (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1990. REVIEWa
  156672. GABRIEL WEATHERHEAD
  156673. 8221N
  156674. 2/28/96V
  156675. COLQUHOUN, H. M.; THOMPSON, D. J.; TWIGG, M. V. CARBONYLATION. DIRECT SYNTHESIS OF CARBONYL COMPOUNDS. PLENUM: NEW YORK, 1991. REVIEWa
  156676. GABRIEL WEATHERHEAD
  156677. 8222N
  156678. 2/28/96VUBROWN, C., ED. CHIRALITY IN DRUG DESIGN AND SYNTHESIS. ACADEMIC: LONDON, 1990. REVIEWa
  156679. GABRIEL WEATHERHEAD
  156680. 8223N
  156681. 2/28/96
  156682. BLOCK, ERIC, ED. CYCLOPHANES (MONOGRAPHS IN SUPRAMOLECULAR CHEMISTRY). ROYAL SOCIETY OF CHEMISTRY CAMBRIDGE, U.K., 1991. REVIEWa
  156683. GABRIEL WEATHERHEAD
  156684. 8224N
  156685. 2/28/96V
  156686. BARTON, DEREK H. R., SIR. SOME RECOLLECTIONS OF GAP JUMPMG (PROFILES, PATHWAYS, AND DREAMS: AUTOBIOGRAPHIES OF EMINENT CHEMISTS). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1990. REVIEWa
  156687. GABRIEL WEATHERHEAD
  156688. 8225N
  156689. 2/28/96VqBALZANI, VINCENZO; SCANDOLA, FRANCO. SUPRAMOLECULAR PHOTOCHEMISTRY. ELLIS HORWOOD: CHICHESTER, U.K., 1991. REVIEWa
  156690. GABRIEL WEATHERHEAD
  156691. 8226N
  156692. 2/28/96V
  156693. PLATZ, MATTHEW S.; LEYVA, ELISA; HAIDER, KARL. SELECTED TOPICS IN THE MATRIX PHOTOCHEMISTRY OF NITRENES, CARBENES, AND EXCITED TRIPLET STATES. ORGANIC PHOTOCHEMISTRY. VOLUME 11, ALBERT PADWA, ED., DEKKER: NEW YORK, 1991. REVIEWa
  156694. GABRIEL WEATHERHEAD
  156695. 8227N
  156696. 2/28/96
  156697. WAGNER, PETER J.; PARK, BONG SER. PHOTOINDUCED HYDROGEN ATOM ABSTRACTION BY CARBONYL COMPOUNDS. ORGANIC PHOTOCHEMISTRY. VOLUME 11, ALBERT PADWA, ED., DEKKER: NEW YORK, 1991. REVIEWa
  156698. GABRIEL WEATHERHEAD
  156699. 8228N
  156700. 2/28/96V
  156701. CHILDS, RONALD F., SHAW, GARY B. THE PHOTOCHEMISTRY OF CARBENIUM IONS AND RELATED SPECIES. ORGANIC PHOTOCHEMISTRY. VOLUME 11, ALBERT PADWA, ED., DEKKER: NEW YORK, 1991. REVIEWa
  156702. GABRIEL WEATHERHEAD
  156703. 8229N
  156704. 2/28/96V
  156705. DEMUTH, MARTIN. SYNTHETIC ASPECTS OF THE OXADI PI METHANE REARRANGEMENT. ORGANIC PHOTOCHEMISTRY. VOLUME 11, ALBERT PADWA, ED., DEKKER: NEW YORK, 1991. REVIEWa
  156706. GABRIEL WEATHERHEAD
  156707. 8230N
  156708. 2/28/96V
  156709. ZIMMERMAN, HOWARD, E. THE DI PI METHANE REARRANGEMENT. ORGANIC PHOTOCHEMISTRY. VOLUME 11, ALBERT PADWA, ED., DEKKER: NEW YORK, 1991. REVIEWa
  156710. GABRIEL WEATHERHEAD
  156711. 8231N
  156712. 2/28/96
  156713. SAUVAGE, J. P.; DIETRICH BUCHECKER C. INTERLOCKED AND KNOTTED RINGS IN BIOLOGY AND CHEMISTRY. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156714. GABRIEL WEATHERHEAD
  156715. 8232N
  156716. 2/28/96V
  156717. CHIN, J., BANASZCZYK, M., JUBIAN, V., KIM, J. H., MREJEN K. ARTIFICIAL HYDROLYTIC METALLOENZYMES: A UNIFIED APPROACH. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156718. GABRIEL WEATHERHEAD
  156719. 8233N
  156720. 2/28/96V
  156721. HAMILTON, A. D. SYNTHETIC STUDIES ON MOLECULAR RECOGNITION. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156722. GABRIEL WEATHERHEAD
  156723. 8234N
  156724. 2/28/96V
  156725. MURAKAMI, Y.; KIKUCHI, J. SUPRAMOLECULAR ASSEMBLIES FORMED WITH SYNTHETIC PEPTIDE LIPIDS. FUNCTIONAL MODELS OF BIOMEMBRANES AND ENZYMES. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156726. GABRIEL WEATHERHEAD
  156727. 8235N
  156728. 2/28/96V
  156729. ZIMMERMAN, S. C. MOLECULAR TWEEZERS: SYNTHETIC RECEPTORS FOR PI SANDWICH COMPLEXATION OF AROMATIC SUBSTRATES. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156730. GABRIEL WEATHERHEAD
  156731. 8236N
  156732. 2/28/96V
  156733. COREY, D. R., ZUCKERMANN, R. N., SCHULTZ, P. G. HYBRID ENZYMES AND THE SEQUENCE SPECIFIC CLEAVAGE OF NUCLEIC ACIDS. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 2, H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1991. REVIEWa
  156734. GABRIEL WEATHERHEAD
  156735. 8237N
  156736. 2/28/96V
  156737. SHINKAI, S. FUNCTIONALIZATION OF CROWN ETHERS AND CALIXARENES: NEW APPLICATIONS AS LIGANDS, CARRIERS AND HOST MOLECULES. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 1,  H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1990. REVIEWa
  156738. GABRIEL WEATHERHEAD
  156739. 8238N
  156740. 2/28/96
  156741. EBMEYER, F.; VOGTLE, F. ON THE WAY FROM SMALL TO VERY LARGE MOLECULAR CAVITIES. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 1,  H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1990. REVIEWa
  156742. GABRIEL WEATHERHEAD
  156743. 8239N
  156744. 2/28/96V
  156745. GOKEL, G. W.; ECBEGOYEN, L. LARIAT ETHERS IN MEMBRANES AND AS MEMBRANES. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 1,  H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1990. REVIEWa
  156746. GABRIEL WEATHERHEAD
  156747. 8240N
  156748. 2/28/96V
  156749. FYLES, T. M. BIOMIMETIC ION TRANSPORT WITH SYNTHETIC TRANSPORTERS. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 1,  H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1990. REVIEWa
  156750. GABRIEL WEATHERHEAD
  156751. 8241N
  156752. 2/28/96V
  156753. BENNER, S. A.; ELLINGTON, A. D. EVOLUTION AND STRUCTURAL THEORY: THE FRONTIER BETWEEN CHEMISTRY AND BIOLOGY. BIOORGANIC CHEMISTRY FRONTIERS. VOLUME 1,  H. DUGAS, ED., SPRINGER VERLAG: BERLIN, 1990. REVIEWa
  156754. GABRIEL WEATHERHEAD
  156755. 8242N
  156756. 2/28/96
  156757. BAUMSTARK, A. L.; BOYKIN, D. W. 17 O NMR SPECTROSCOPY APPLICATIONS TO STRUCTURAL PROBLEMS IN ORGANIC CHEMISTRY. ADVANCES IN OXYGENATED PROCESSES, VOLUME 3 ALFONS L. BAUMSTARK, ED., JAI PRESS, INC.: GREENWICH, CT, 1991. REVIEWa
  156758. GABRIEL WEATHERHEAD
  156759. 8243N
  156760. 2/28/96V
  156761. TU, S. C. OXYGENATED FLAVIN INTERMEDIATES OF BACTERIAL LUCIFERASE AND FLAVOPROTEIN AROMATIC HYDROXYLASES: ENZYMOLOGY AND CHEMICAL MODELS. ADVANCES IN OXYGENATED PROCESSES, VOLUME 3 ALFONS L. BAUMSTARK, ED., JAI PRESS, INC.: GREENWICH, CT, 1991. REVIEWa
  156762. GABRIEL WEATHERHEAD
  156763. 8244N
  156764. 2/28/96V
  156765. EISENBERG, W. C. ATMOSPHERIC GAS PHASE GENERATION OF SINGLET DELTA OXYGEN. ADVANCES IN OXYGENATED PROCESSES, VOLUME 3 ALFONS L. BAUMSTARK, ED., JAI PRESS, INC.: GREENWICH, CT, 1991. REVIEWa
  156766. GABRIEL WEATHERHEAD
  156767. 8245N
  156768. 2/28/96
  156769. HOFFMAN, R. V. OXIDATIVE ATTACHMENT OF ARENESULFONYLOXY GROUPS WITH ARENESULFONYL PEROXIDES. ADVANCES IN OXYGENATED PROCESSES, VOLUME 3 ALFONS L. BAUMSTARK, ED., JAI PRESS, INC.: GREENWICH, CT, 1991. REVIEWa
  156770. GABRIEL WEATHERHEAD
  156771. 8246N
  156772. 2/28/96V
  156773. KUCZKOWSKI, R. L. OZONOLYSIS OF VINYL ETHERS. ADVANCES IN OXYGENATED PROCESSES, VOLUME 3 ALFONS L. BAUMSTARK, ED., JAI PRESS, INC.: GREENWICH, CT, 1991. REVIEWa
  156774. GABRIEL WEATHERHEAD
  156775. 8247N
  156776. 2/28/96V
  156777. FLOSS, HEINZ G., STROHL, WILLIAM R. GENETIC ENGINEERING OF HYBRID ANTIBIOTICS. A PROGRESS REPORT. 1991, 47(31), 6045 58. TETRAHEDRON REVIEWa
  156778. GABRIEL WEATHERHEAD
  156779. 8248N
  156780. 2/28/96V
  156781. YONEDA, NORIHIKO. THE COMBINATION OF HYDROGEN FLUORIDE WITH ORGANIC BASES AS FLUORINATION AGENTS. 1991, 47(29), 5329 65. TETRAHEDRON REVIEWa
  156782. GABRIEL WEATHERHEAD
  156783. 8249N
  156784. 2/28/96
  156785. V|CROSBY, JOHN. SYNTHESIS OF OPTICALLY ACTIVE COMPOUNDS: A LARGE SCALE PERSPECTIVE. 1991, 47(27), 4789 846. TETRAHEDRON REVIEWa
  156786. GABRIEL WEATHERHEAD
  156787. 8250N
  156788. 2/28/96VxTHOMPSON, CHARLES M.; GREEN, DIANA L. C. RECENT ADVANCES IN DIANION CHEMISTRY. 1991, 47(25), 4223 85. TETRAHEDRON REVIEWa
  156789. GABRIEL WEATHERHEAD
  156790. 8251N
  156791. 2/28/96V
  156792. CORDELL, GEOFFREY; KINGHORN, A. DOUGLAS. ONE DIMENSIONAL PROTON CARBON CORRELATIONS FOR THE STRUCTURE DETERMINATION OF NATURAL PRODUCTS. 1991, 47(22), 3521 34. TETRAHEDRON REVIEWa
  156793. GABRIEL WEATHERHEAD
  156794. 8252N
  156795. 2/28/96V
  156796. MIKAMI KOICHI  NAKAI, TAKESHI. ACYCLIC STEREOCONTROL VIA [2,3] WITTIG SIGMATROPIC REARRANGEMENT. 1991, (8), 594 6O4. SYNTHESIS REVIEWa
  156797. GABRIEL WEATHERHEAD
  156798. 8253N
  156799. 2/28/96VsDENINNO, MICHAEL P. THE SYNTHESIS AND GLYCOSIDATION OF N ACETYLNEURAMINIC ACID. 1991, (8), 583 93. SYNTHESIS REVIEWa
  156800. GABRIEL WEATHERHEAD
  156801. 8254N
  156802. 2/28/96
  156803. DRUECKHAMMER, DALE G.; HENNEN, WILLIAM J.; PEDERSON, RICHARD L.; BARBAS, CARLOS F. III; GAUTHERON, CHRISTINE M.; KRACH, THOMAS; WONG, CHI HUEY. ENZYME CATALYSIS IN SYNTHETIC CARBOHYDRATE CHEMISTRY. 1991, (7), 499 525. SYNTHESIS REVIEWa
  156804. GABRIEL WEATHERHEAD
  156805. 8255N
  156806. 2/28/96V
  156807. TAMURA, RUI; KAMIMURA, AKIO; ONO, NOBORU. DISPLACEMENT OF ALIPHATIC NITRO GROUPS BY CARBON AND HETEROATOM NUCLEOPHILES. 1991, (6), 423 34. SYNTHESIS REVIEWa
  156808. GABRIEL WEATHERHEAD
  156809. 8256N
  156810. 2/28/96VaNAKAMURA EIICHI. NEW TOOLS IN SYNTHETIC ORGANOCOPPER CHEMISTRY. 1991, (8), 539 47. SYNLETT REVIEWa
  156811. GABRIEL WEATHERHEAD
  156812. 8257N
  156813. 2/28/96V}MASH, EUGENE A. STEREOCONTROLLED MANIPULATIONS OF CHROMATOGRAPHICALLY RESOLVED PYRANOSIDES. 1991, (8), 529 38. SYNLETT REVIEWa
  156814. GABRIEL WEATHERHEAD
  156815. 8258N
  156816. 2/28/96VjPHILP, DOUGLAS; STODDART, J. FRASER. SELF ASSEMBLY IN ORGANIC SYNTHESIS. 1991, (7), 445 58. SYNLETT REVIEWa
  156817. GABRIEL WEATHERHEAD
  156818. 8259N
  156819. 2/28/96V{GROTJAHN, D. B.; DOTZ, K. H. CARBENE COMPLEXES OF CHROMIUM BEARING NITROGEN SUBSTITUENTS. 1991, (6), 381 90. SYNLETT REVIEWa
  156820. GABRIEL WEATHERHEAD
  156821. 8260N
  156822. 2/28/96
  156823. ASTRUC, DIDIER. THE TRANSFORMATION OF AROMATICS INTO REGIO  AND STEREOCONTROLLED HETEROBIFUNCTIONAL CYCLOHEXADIENES MEDIATED BY TEMPORARY SANDWICH COMPLEXATION. ROLES OF ELECTRON, PROTON, HYDRIDE AND HYDROGEN ATOM TRANSFERS. 1991, (6), 369 80. SYNLETT REVIEW
  156824. GABRIEL WEATHERHEAD
  156825. 8261N
  156826. 2/28/96V
  156827. PANETTA, CHARLES A.; HEIMER, NORMAN E.; HUSSEY, CHARLES L.; METZGER, ROBERT M. FUNCTIONALIZED TETRACYANOQUINODIMETHANE TYPE ELECTRON ACCEPTORS: SUITABLE PRECURSORS FOR D SIGMA A MATERIALS. 1991, (5), 301 309. SYNLETT REVIEWa
  156828. GABRIEL WEATHERHEAD
  156829. 8262N
  156830. 2/28/96V}GRIBBLE, GORDON W. APPROACHES TO THE SYNTHESIS OF THE ANTITUMOR PYRIDOCARBAZOLE ALKALOIDS. 1991, (5), 289 300. SYNLETT REVIEWa
  156831. GABRIEL WEATHERHEAD
  156832. 8263N
  156833. 2/28/96VyROSEN, TERRY; NAGEL, ARTHUR A.; RIZZI, JAMES P. NOVEL SEROTONIN 3 RECEPTOR ANTNGONISTS. 1991, (4), 213 21. SYNLETT REVIEWa
  156834. GABRIEL WEATHERHEAD
  156835. 8264N
  156836. 2/28/96V
  156837. BARRY, CLIF E. III; BATES, ROBERT B.; BEAVERS, WILLIAM A.; CAMOU, FERNANDO A.; GORDON, BERNARD, III; HSU, HOWARD F. J.; MILLS, NANCY S.; ET AL. DELOCALIZED CARBANIONS IN SYNTHESIS. 1991, (4), 207 12. SYNLETT REVIEWa
  156838. GABRIEL WEATHERHEAD
  156839. 8265N
  156840. 2/28/96V
  156841. MANDER, LEWIS N. EXPLOITATION OF ARYL SYNTHONS IN THE SYNTHESIS OF POLYCYCLIC NATURAL PRODUCTS. 1991, (3),134 44. SYNLETT REVIEWa
  156842. GABRIEL WEATHERHEAD
  156843. 8266N
  156844. 2/28/96V
  156845. SESSLER, J. L.; CYR, M. J.; BURRELL, A. K. SAPPHYRNS: NEW LIFE FOR AN OLD "EXPANDED PORPHYRIN". 1991, (3), 127 34. SYNLETT REVIEWa
  156846. GABRIEL WEATHERHEAD
  156847. 8267N
  156848. 2/28/96VsMARCHAMD, ALAN P. POLYCYCLIC CAGE COMPOUNDS AS INTERMEDIATES IN ORGANIC SYNTHESIS. 1991, (2), 73 79. SYNLETT REVIEW
  156849. GABRIEL WEATHERHEAD
  156850. 8268N
  156851. 2/28/96V`CURRAN, DENNIS P. RADICAL REACTIONS AND RETROSYNTHETIC PLANNING. 1991 (2), 63 72. SYNLETT REVIEWa
  156852. GABRIEL WEATHERHEAD
  156853. 8269N
  156854. 2/28/96V
  156855. KUTNEY, JAMES P. PLANT CELL CULTURES AND SYNTHETIC CHEMISTRY A POTENTIALLY POWERFUL ROUTE TO COMPLEX NATURAL PRODUCTS. 1991, (1), 11 19. SYNLETT REVIEWa
  156856. GABRIEL WEATHERHEAD
  156857. 8270N
  156858. 2/28/96V
  156859. HERNDON, JAMES W.; WU, CHAO; HARP, JILL J.; KREUTZER, KRISTINA A. EXPLORATION OF THE [3 + 2] CYCLOADDITION REACTION BETWEEN ALLYLSTANNANES AND ALPHA, BETA UMSATURATED ACYLIRON COMPLEXES. 1991, (1), 1 10. SYNLETT REVIEWa
  156860. GABRIEL WEATHERHEAD
  156861. 8271N
  156862. 2/28/96V
  156863. DUBOIS, JACQUES EMILE; COSSE BARBI, ALIETTE. STRAIN RELEASE IN CONFORMATIONAL AND GEOMETRIC ADAPTATION OF MODERATELY AND HIGHLY CONGESTED SYSTEMS: INTERPLAY OF SMALL STRUCTURAL EFFECTS. 1991, 2, 89 105. STRUCTURAL CHEMISTRY REVIEWa
  156864. GABRIEL WEATHERHEAD
  156865. 2/28/96V
  156866. KLEBE, GERHARD. THE USE OF CRYSTAL DATA TOGETHER WITH OTHER EXPERIMENTAL AND COMPUTATIONAL RESULTS TO DISCUSS STRUCTURE REACTIVITY AND ACTIVITY RELATIONSHIPS. 1990, 1, 597 616. STRUCTURAL CHEMISTRY REVIEWa
  156867. GABRIEL WEATHERHEAD
  156868. 8273N
  156869. 2/28/96VzGREENBERG, ARTHUR; WU GUANLI. STRUCTURAL RELATIONSHIPS IN SILATRANE MOLECULES. 1990, 1, 79 85. STRUCTURAL CHEMISTRY REVIEWa
  156870. GABRIEL WEATHERHEAD
  156871. 8274N
  156872. 2/28/96VuKUTYREV, A. A.; MOSKVA, V. V. NUCLEOPHILIC REACTIONS OF QUINONES. 1991, 60(1), 72 78. RUSSIAN CHEMICAL REVIEWS REVIEWa
  156873. GABRIEL WEATHERHEAD
  156874. 8275N
  156875. 2/28/96V
  156876. MARETINA, I. A. SYNTHETIC ASPECTS OF THE CHEMISTRY OF P,PI UNSATURATED AMINES. 1991, 60(1), 57 71. RUSSIAN CHEMICAL REVIEWS REVIEWa
  156877. GABRIEL WEATHERHEAD
  156878. 8276N
  156879. 2/28/96
  156880. KHRISTOV, V. KH.; ANGELOV, KH. M.; PETROV, A. A. 1,3 ALKADIENES AND THEIR DERIVATIVES IN REACTIONS WITH ELECTROPHILIC REAGENTS. 1991, 60(1), 39 56. RUSSIAN CHEMICAL REVIEWS REVIEWa
  156881. GABRIEL WEATHERHEAD
  156882. 8277N
  156883. 2/28/96V
  156884. BANERJEE, AJAY KUMAR; GONZALEZ, NIEVES CANUDAS. METHODS FOR ANGULAR ALKOXYCARBONYLATION IN FUSED RINGS AND ITS APPLICATION TO THE SYNTHESIS OF TERPENOID COMPOUNDS. 1991, 110(9), 353 67. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS REVIEWa
  156885. GABRIEL WEATHERHEAD
  156886. 8278N
  156887. 2/28/96V
  156888. DOYLE, MICHAEL P. CHIRAL CATALYSTS FOR ENANTIOSELECTIVE CARBENOID CYCLOPROPANATION REACTIONS. 1991, 110(7 8), 305 16. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS REVIEWa
  156889. GABRIEL WEATHERHEAD
  156890. 8279N
  156891. 2/28/96
  156892. NAEFF, HAN S. D.; FRANSSEN, MAURICE C. R.; VAN DER PLAS HENK C. QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIP (QSAR) STUDIES OF THE INHIBITION OF XANTHINE OXIDASE BY HETEROCYCLIC COMPOUNDS. 1991,110(5),139 50. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS REVIEW
  156893. GABRIEL WEATHERHEAD
  156894. 8280N
  156895. 2/28/96V
  156896. ELFERINK, V. H. M.; BREITGOFF, D.; KLOOSTERMNN, M.; KAMPHUIS, J.; VAN DEN TWEEL, W. J. J.; MEIJER, E. M. INDUSTRIAL DEVELOPMENTS IN BIOCATALYSIS. 1991,110(3), 63 74. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS REVIEWa
  156897. GABRIEL WEATHERHEAD
  156898. 8281N
  156899. 2/28/96V
  156900. SCHOEMAKER, H. E. ON THE CHEMISTRY OF LIGNIN BIODEGRADATION. 1990,109(4), 255 72. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS REVIEWa
  156901. GABRIEL WEATHERHEAD
  156902. 8282N
  156903. 2/28/96V
  156904. KAGAN, J. NATURALLY OCCURRING DI  AND TRITHIOPHENES. 1991, 56, 87 169. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS REVIEWa
  156905. GABRIEL WEATHERHEAD
  156906. 8283N
  156907. 2/28/96
  156908. ASSELINEAU, J. BACTERIAL LIPIDS CONTAINING AMINO ACIDS OR PEPTIDES LINKED BY AMIDE BONDS. 1991, 56,1 85. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS REVIEWa
  156909. GABRIEL WEATHERHEAD
  156910. 8284N
  156911. 2/28/96V
  156912. PADWA, ALBERT; MURPHREE, S. SHAUM. RECENT DEVELOPMENTS IN THE AREA OF ANNULATED FURANS. 1991, 23(4), 545 68. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL REVIEWa
  156913. GABRIEL WEATHERHEAD
  156914. 8285N
  156915. 2/28/96V
  156916. SWINDELL, CHARLES S. TAXANE DITERPENE SYNTHESIS STRATEGIES. 1991, 23(4), 465 543. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL REVIEWa
  156917. GABRIEL WEATHERHEAD
  156918. 8286N
  156919. 2/28/96VpGLOTTER, E. WITHANOLIDES AND RELATED ERGOSTANE TYPE STEROIDS. 1991, 8(4), 415 40. NATURAL PRODUCT REPORTS REVIEWa
  156920. GABRIEL WEATHERHEAD
  156921. 8287N
  156922. 2/28/96VjMARSTON, A.; HOSTETTMANN, K. MODERN SEPNRATION METHODS 1991, 8(4), 391 413. NATURAL PRODUCT REPORTS REVIEWa
  156923. GABRIEL WEATHERHEAD
  156924. 8288N
  156925. 2/28/96
  156926. ViBROOKS, C. J. W.; WATSON, D. G. TERPENOID PHYTOALEXINS 1991, 8(4), 367 89. NATURAL PRODUCT REPORTS REVIEWa
  156927. GABRIEL WEATHERHEAD
  156928. 8289N
  156929. 2/28/96VxBENTLEY, K. W. BETA PHENYLETHYLAMINES AND THE ISOQUINOLINE ALKALOIDS. 1991, 8(4), 339 66. NATURAL PRODUCT REPORTS REVIEWa
  156930. GABRIEL WEATHERHEAD
  156931. 8290N
  156932. 2/28/96V|JANSEN, B. J. M.; DE GROOT, A. THE SYNTHESIS OF DRIMANE SESQUITERPENOIDS. 1991, 8(3), 319 37. NATURAL PRODUCT REPORTS REVIEWa
  156933. GABRIEL WEATHERHEAD
  156934. 8291N
  156935. 2/28/96V
  156936. JAMSEN, B. J. M.; DE GROOT, A. THE OCCURRENCE AND BIOLOGICAL ACTIVITY OF DRIMANE SESQUITERPENOIDS. 1991, 8(3), 309 18. NATURAL PRODUCT REPORTS REVIEWa
  156937. GABRIEL WEATHERHEAD
  156938. 8292N
  156939. 2/28/96V
  156940. SAXTON, J. E. RECENT PROGRESS IN THE CHEMISTRY OF INDOLE ALKALOIDS  AND MOLD METABOLITES. 1991, 8(3), 251 307. NATURAL PRODUCT REPORTS REVIEWa
  156941. GABRIEL WEATHERHEAD
  156942. 8293N
  156943. 2/28/96
  156944. V]BRITTON,G. CAROTENOIDS AND POLYTERPENOIDS. 1991, 8(3), 223 49. NATURAL PRODUCT REPORTS REVIEWa
  156945. GABRIEL WEATHERHEAD
  156946. 8294N
  156947. 2/28/96VYROBINS, D. J. PYRROLIZIDINE ALKALOIDS. 1991, 8(3), 213 21. NATURAL PRODUCT REPORTS REVIEWa
  156948. GABRIEL WEATHERHEAD
  156949. 8295N
  156950. 2/28/96V
  156951. HERBERT, R. B. THE BIOSYNTHESIS OF PLANT ALKALOIDS AND NITROGENOUS MICROBIAL METABOLITES. 1991, 8(2), 185 209. NATURAL PRODUCT REPORTS REVIEWa
  156952. GABRIEL WEATHERHEAD
  156953. 8296N
  156954. 2/28/96V
  156955. LEWIS, J. R. MUSCARINE, OXAZOLE, THIAZOLE, IMIDAZOLE, AND PEPTIDE ALKALOIDS, AND OTHER MISCELLANEOUS ALKALOIDS. 1991, 8(2), 171 83. NATURAL PRODUCT REPORTS REVIEWa
  156956. GABRIEL WEATHERHEAD
  156957. 8297N
  156958. 2/28/96VkDEWICK, P. M. THE BIOSYNTHESIS OF SHIKIMATE METABOLITES. 1991, 8(2), 149 70. NATURAL PRODUCT REPORTS REVIEWa
  156959. GABRIEL WEATHERHEAD
  156960. 8298N
  156961. 2/28/96V[FAULKNER, D. J. MARINE NATURAL PRODUCTS. 1991, 8(2), 97 147. NATURAL PRODUCT REPORTS REVIEW
  156962. GABRIEL WEATHERHEAD
  156963. 8299N
  156964. 2/28/96V^PFANDER, H.; STOLL, H. TERPENOID GLYCOSIDES. 1991, 8(1), 69 95. NATURAL PRODUCT REPORTS REVIEWa
  156965. GABRIEL WEATHERHEAD
  156966. 8300N
  156967. 2/28/96VpMICHAEL, J. P. QUINOLINE, QUINAZOLINE, AND ACRIDONE ALKALOIDS. 1991, 8(1), 53 68. NATURAL PRODUCT REPORTS REVIEWa
  156968. GABRIEL WEATHERHEAD
  156969. 8301N
  156970. 2/28/96VjTURNER, A. B. STEROIDS: REACTIONS AND PARTIAL SYNTHESIS. 1991, 8(1), 17 52. NATURAL PRODUCT REPORTS REVIEWa
  156971. GABRIEL WEATHERHEAD
  156972. 8302N
  156973. 2/28/96VLHANSON, J. R. DITERPENOIDS. 1991, 8(1), 1 16. NATURAL PRODUCT REPORTS REVIEWa
  156974. GABRIEL WEATHERHEAD
  156975. 8303N
  156976. 2/28/96V
  156977. BOX, VERNON G. S. THE ROLE OF LONE PAIR INTERACTIONS IN THE CHEMISTRY OF THE MONOSACCHARIDES. STEREO ELECTRONIC EFFECTS IN UNSATURATED MONOSACCHARIDES. 1991, 32(4), 795 807. HETEROCYCLES REVIEWa
  156978. GABRIEL WEATHERHEAD
  156979. 8304N
  156980. 2/28/96
  156981. ALVAREZ, MERCEDES; SALAS, MARISA; JOULE, JOHN A. MARINE NITROGEN CONTAINING HETEROCYCLIC NATURAL PRODUCTS. STRUCTURES AND SYNTHESES OF COMPOUNDS CONTAINING QUINOLINE AND/OR ISOQUINOLINE UNITS. 1991, 32(4), 759 94. HETEROCYCLES REVIEWa
  156982. GABRIEL WEATHERHEAD
  156983. 8305N
  156984. 2/28/96V
  156985. KATRITZKY, ALAN R.; KARELSON, MATI; HARRIS, PHILIP A. PROTOTROPIC TAUTOMERISM OF HETEROAROMATIC COMPOUNDS. 1991, 32(2), 329 69. HETEROCYCLES REVIEWa
  156986. GABRIEL WEATHERHEAD
  156987. 8306N
  156988. 2/28/96VyKATRITZKY, ALAM R; KARELSON, MATI; MALHOTRA, NAGESHWAR. HETEROCYCLIC AROMATICITY. 1991, 32(1),127 61. HETEROCYCLES REVIEWa
  156989. GABRIEL WEATHERHEAD
  156990. 8307N
  156991. 2/28/96V
  156992. PEET, NORTON P.; LETOURNEAU, MICHAEL E. SYNTHESIS OF ANGULAR BENZODIPYRAZOLES AND RELATED SYSTEMS. 1991, 32(1), 41 72. HETEROCYCLES REVIEWa
  156993. GABRIEL WEATHERHEAD
  156994. 8308N
  156995. 2/28/96VkROBERTS, STANLEY M. SUGAR MIMICS POTENTIAL ANTI INFECTIVES 1991, 27(6), 518 20. CHEMISTRY IN BRITAIN REVIEW
  156996. GABRIEL WEATHERHEAD
  156997. 8309N
  156998. 2/28/96V
  156999. COOPER, DAVID L., ROBB, MICHAEL A., WILLIAMS, IAN H. ORGANIC REACTIVITY NEW LIGHT ON OLD CONCEPTS. 1990, 26(11), 1085 9 CHEMISTRY IN BRITAIN REVIEWa
  157000. GABRIEL WEATHERHEAD
  157001. 8310N
  157002. 2/28/96V
  157003. JASPERSE, CRAIG P.; CURRAN, DENNIS P.; FEVIG, THOMAS L. RADICAL REACTIONS IN NATURAL PRODUCT SYNTHESIS. 1991, 91(6), 1237 86. CHEMICAL REVIEWS REVIEWa
  157004. GABRIEL WEATHERHEAD
  157005. 8311N
  157006. 2/28/96VpKROTO, H. W.; ALLAF, A. W.; BALM, S. P. C60: BUCKMINSTERFULLERENE. 1991, 91 (6),1213 35. CHEMICAL REVIEWS REVIEWa
  157007. GABRIEL WEATHERHEAD
  157008. 8312N
  157009. 2/28/96V
  157010. BURGESS, KEVIN; OHLMEYER, MICHAEL J. TRANSITION METAL PROMOTED HYDROBORATIONS OF ALKENES, EMERGING METHODOLOGY FOR ORGANIC TRANSFORMATIONS. 1991, 91(6), 1179 91. CHEMICAL REVIEWS REVIEWa
  157011. GABRIEL WEATHERHEAD
  157012. 8313N
  157013. 2/28/96
  157014. VxELLER, KARSTEN; SCHWARZ, HELMUT. ORGANOMETALLIC CHEMISTRY IN THE GAS PHASE. 1991, 91(6),1121 77. CHEMICAL REVIEWS REVIEWa
  157015. GABRIEL WEATHERHEAD
  157016. 8314N
  157017. 2/28/96V
  157018. BADER, RICHARD F. W. A QUANTUM THEORY OF MOLECULAR STRUCTURE AND ITS APPLICATIONS. 1991. 91(5), 893 928. CHEMICAL REVIEWS REVIEWa
  157019. GABRIEL WEATHERHEAD
  157020. 8315N
  157021. 2/28/96V
  157022. ORLANDI, GIORGIO; ZERBETTO, FRANCESCO; ZGIERSKI, MAREK Z. THEORETICAL ANALYSIS OF SPECTRA OF SHORT POLYENES. 1991 91(5), 867 91. CHEMICAL REVIEWS REVIEWa
  157023. GABRIEL WEATHERHEAD
  157024. 8316N
  157025. 2/28/96V
  157026. NEWTON, MARSHALL D. QUANTUM CHEMICAL PROBES OF ELECTRON TRANSFER KINETICS: THE NATURE OF DONOR ACCEPTOR INTERACTIONS. 1991, 91(5), 767 92. CHEMICAL REVIEWS REVIEWa
  157027. GABRIEL WEATHERHEAD
  157028. 8317N
  157029. 2/28/96V
  157030. VEILLARD, ALAIN. AB INITIO CALCULATIONS OF TRANSITION METAL ORGANOMETALLICS: STRUCTURE AND MOLECULAR PROPERTIES. 1991 91(5), 743 66. CHEMICAL REVIEWS REVIEWa
  157031. GABRIEL WEATHERHEAD
  157032. 8318N
  157033. 2/28/96V
  157034. NICOLAOU, K. C.; RAMPHAL, J. Y.; PETASIS, N. A.; SERHAN, C. N. LIPOXINS AND RELATED EICOSANOIDS: BIOSYNTHESIS, BIOLOGICAL PROPERTIES, AND CHEMICAL SYNTHESIS. 1991, 30(9),1100 16. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEWa
  157035. GABRIEL WEATHERHEAD
  157036. 8319N
  157037. 2/28/96V
  157038. MENGER, F. M. GROUPS OF ORGANIC MOLECULES THAT OPERATE COLLECTIVELY. 1991, 30(9), 1086 99. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEWa
  157039. GABRIEL WEATHERHEAD
  157040. 8320N
  157041. 2/28/96V
  157042. RYABOV, ALEXANDER D. THE BIOCHEMICAL REACTIONS OF ORGANOMETALLICS WITH ENZYMES. 1991, 30(8), 931 941. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEWa
  157043. GABRIEL WEATHERHEAD
  157044. 8321N
  157045. 2/28/96
  157046. RUCHARDT, CHRISTOPH; MEIER, MICHAEL; HAAF, KLAUS, PAKUSCH, JOACHIM; WOLBER, ERWIN K A.; MULLER, BARBARA. THE ISOCYANIDE CYANIDE REARRANGEMENT; MECHANISM AND PREPARATIVE APPLICATIONS. 1991, 30(8), 893 901. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEW
  157047. GABRIEL WEATHERHEAD
  157048. 8322N
  157049. 2/28/96V
  157050. EUGSTER, CONRAD H.; MARKI FISCHER, EDITH. THE CHEMISTRY OF ROSE PIGMENTS. 1991, 30(6), 654 72. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEWa
  157051. GABRIEL WEATHERHEAD
  157052. 8323N
  157053. 2/28/96V
  157054. ENGLISCH. UWE; GAUSS, DIETER H. CHEMICALLY MODIFIED OLIGONUCLEOTIDES AS PROBES AND INHIBITORS. 1991, 30(6) 612 29. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH REVIEWa
  157055. GABRIEL WEATHERHEAD
  157056. 8324N
  157057. 2/28/96VyCARUTHERS, MARVIN H. CHEMICAL SYNTHESIS OF DNA AND DNA ANALOGS. 1991, 24(9), 278 84. ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  157058. GABRIEL WEATHERHEAD
  157059. 8325N
  157060. 2/28/96
  157061.     VbBLEEKE, JOHN R. METALLABENZENE CHEMISTRY. 1991, 24(9), 271 7. ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  157062. GABRIEL WEATHERHEAD
  157063. 8326N
  157064. 2/28/96V
  157065. WALLING, CHEVES. THE NATURE OF RADICALS INVOLVED IN GRIGNARD REAGENT FORMATION 1991, 24(9), 255 6. ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  157066. GABRIEL WEATHERHEAD
  157067. 8327N
  157068. 2/28/96V
  157069. THOMAS, ERIC J. CYTOCHALASAN SYNTHESIS: MACROCYCLE FORMATION VIA INTRAMOLECULAR DIELS ALDER REACTIONS. 1991, 24(8), 229 35. ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  157070. GABRIEL WEATHERHEAD
  157071. 8328N
  157072. 2/28/96V
  157073. BERSON, JEROME A. THE OVERLAP COMPONENT OF THE STEREOELECTRONIC FACTOR. REMOTE CONTROL OF STEREOGENICITY TRANSFER THROUGH THE ANISOTROPIC INFLUENCE OF A RING. 1991 24(7), 215 22. ACCOUNTS OF CHEMICAL RESEARCH REVIEWa
  157074. GABRIEL WEATHERHEAD
  157075. 8329N
  157076. 2/28/96V
  157077. OAE, SHIGERU; UCHIDA, YUZURU. LIGAND COUPLING REACTIONS OF HYPERVALENT SPECIES. 1991, 24(7), 202 8. ACCOUNTS OF CHEMICAL RESEARCH REVIEW
  157078. GABRIEL WEATHERHEAD
  157079. ORG PREP PROCEDURE INTC
  157080. DIELS ALDER REACTION AMINO ACID ANALYSIS EPOXY RESINS CONVENIENT SYNTHESIS ORGANOMETALLIC COMPOUNDS PROTEIN HYDROLYSIS PULSED IRRADIATION INORGANIC SOLIDS OPIUM ALKALOIDS OVEN ABRAMOVITCH RAM
  157081. 8330N
  157082. 2/28/96VAAPPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY   A REVIEW.W
  157083. 1991 DECX
  157084. 685 711Y
  157085. 23(6)a
  157086. GABRIEL WEATHERHEAD
  157087. ANGEW. CHEM.C6NICKEL CATALYZED NICKEL REVIEW  KEIM ORGANONICKEL KEIMM
  157088. 8331N
  157089. 2/28/96VNNICKEL: AN ELEMENT WITH WIDE APPLICATIONS IN INDUSTRIAL HOMOGENEOUS CATALYSIS.W
  157090. INT. VOL 29   1990  P 235a
  157091. GABRIEL WEATHERHEAD
  157092. ORG PREP PROCEDURE INTC9LEAD TETRAACETATE DIOXIMES DERIVATIVES COMPLEXES KOTALI AM
  157093. 8332N
  157094. 2/28/96V/THE CHEMISTRY OF 1,3 DIOXIMES   A BRIEF REVIEW.W
  157095. 1991 OCTX
  157096. 593 610Y
  157097. 23(5)a
  157098. GABRIEL WEATHERHEAD
  157099. ORG PREP PROCEDURE INT
  157100. DIELS ALDER REACTIONS CYCLOADDITION REACTIONS SYN SESQUINORBORNATRIENE ORGANIC SYNTHESIS DOUBLE BOND PHOTOELECTRON SPECTROSCOPY <4>PERISTYLANE PERIMETER ORBITAL INTERACTIONS HIGH PRESSURE BIS SULFONES COSSU SM
  157101. 8333N
  157102. 2/28/96V(1,2 BIS(ARYLSULFONYL)ALKENES   A REVIEW.W
  157103. 1991 OCTX
  157104. 571 592Y
  157105. 23(5)a
  157106. GABRIEL WEATHERHEAD
  157107. AUST J CHEMC
  157108. BETA DICARBONYL COMPOUNDS ARYL LEAD TRIACETATES ARYLLEAD(IV) TRICARBOXYLATES NITRONATE SALTS COUPLING REACTIONS ALK 1 ENYL LEAD TRIACETATES ELECTROPHILIC ARYLATION CONVENIENT ROUTE COPPER CATALYSIS FACILE SYNTHESIS PINHEY JTM
  157109. 8334N
  157110. 2/28/96VTORGANOLEAD(IV) TRICARBOXYLATES, NEW REAGENTS FOR ORGANIC SYNTHESIS   INVITED REVIEW.W
  157111. 1991X    1353 1382Y
  157112. 44(10)a
  157113. GABRIEL WEATHERHEAD
  157114. TET LETTCZEPOXIDE CHIRAL ASYMMETRIC GRIGNARD NITRILE KETO ADDITION CYANO DIASTEREOSELECTIVITY REVIEWM
  157115. 8335N
  157116. 2/28/96V(A NEW ROUTE TO CHIRAL EPOXY BUTANE DIOLSW
  157117. P 6731  1991a
  157118. GABRIEL WEATHERHEAD
  157119. TET LETT
  157120. CDEPOXIDE ALKYNE ACETYLIDE RING OPENING REVIEW CARBANION METAL ALCOHOLM
  157121. 8336N
  157122. 2/28/96VGSTEREO AND REGIOSELECTIVE METAL SALT CATALYZED ALKYNYLATION OF EPOXIDESW
  157123. P 6617  1991a
  157124. GABRIEL WEATHERHEAD
  157125. JACSC=FISCHER CHROMIUM CARBENE COMPLEX REVIEW WRITING ALKYNE PHENOLM
  157126. 8337N
  157127. 2/28/96VmSUBSTRATE REGULATION OF PRODUCT DISTRIBUTION IN THE REACTIONS OF ARYL CHROMIUM CARBENE COMPLEXES WITH ALKYNESW
  157128. VOL 113  P 9293  1991a
  157129. GABRIEL WEATHERHEAD
  157130. JOCCWHOFFMAN TRICARBONYL PREPARATION REVIEW WRITING EXPERIMENTAL KETO AMIDE STUDENT NEW IDEAM
  157131. 8338N
  157132. 2/28/96VrA SIMPLE SYNTHESIS OF 1,2,3 TRICARBONYL COMPOUNDS 2,3 DIKETO AMIDES USING P NITROBENZENE SULFINIC ACID ELIMINATIONW
  157133. VOL 56 P 6435 1991a
  157134. GABRIEL WEATHERHEAD
  157135. WENDER INTRAMOLECULAR DIPOLAR CYCLOADDITION DIPOLE CARBONYL YLIDE PYRYLIUM OXIDE REVIEW PHORBOL ZWITTERION CYCLOADDITION SALT FLUORIDEM
  157136. 8339N
  157137. 2/28/96
  157138. A NEW 5+2 CYCLOADDITION METHOD AND ITS APPLICATION TO THE SYNTHESIS OF PHORBOL AND ITS DERIVATIVES USING A PYRLIUM OXIDE DIPOLEW
  157139. VOL 56 P 6267 1991a
  157140. GABRIEL WEATHERHEAD
  157141. TETRAHEDRONCPREVIEW LACTAM REARRANGEMENT REGIOSELECTIVE RING EXPANSION OXIME HETEROCYCLE KROWM
  157142. 8340N
  157143. 2/28/96V7NITROGEN INSERTION REACTION OF BRIDGED BICYCLIC KETONESW
  157144. VOL 37 P 1283 1981a
  157145. GABRIEL WEATHERHEAD
  157146. JACSCeEPOXIDE EPOXIDATION CHIRAL CATALYST REVIEW ASYMMETRIC INDUCTION ENANTIOSELECTIVITY SHARPLESS JACOBSENM
  157147. 8341N
  157148. 2/28/96VQHIGHLY ENANTIOSELECTIVE EPOXIDATION CATALYSTS DERIVED FROM 1,2 DIAMINOCYCLOHEXANEW
  157149. 1991 VOL. 113 P. 7063a
  157150. GABRIEL WEATHERHEAD
  157151. JACSC]FLASH VACUUM PYROLYSIS SPRAY ALKYNE CYCLOBUTANE TECHNIQUE METHOD EXPERIMENTAL REVIEW DIEDRICHM
  157152. 8342N
  157153. 2/28/96VJSOLUTION SPRAY FLASH VACUUM PYROLYSIS. A NEW METHOD TO PREPARE POLYALKYNESW
  157154. 1991 VOL. 113 P. 6943a
  157155. GABRIEL WEATHERHEAD
  157156. SYN. LETT.
  157157. CvCONJUGATE ADDITION CUPRATE COPPER REVIEW CATALYZED REAGENT CHIRAL ENONE HOMOENOLATE SILICON SILYL CYCLOPROPYL NAKAMURAM
  157158. 8343N
  157159. 2/28/96VNCHLOROTRIMETHYL SILYL ACCELERATED CONJUGATE ADDITION OF ORGANO COPPER REAGENTSW
  157160. 1991 P. 539a
  157161. GABRIEL WEATHERHEAD
  157162. BULL. SOC. CHIM. FR.CCRADICAL STEREOCHEM SILICON CYCLIZATION REVIEW ACETAL TIN HALO STORKM
  157163. 8344N
  157164. 2/28/96V
  157165. A SURVEY OF RADICAL MEDIATED CYCLIZATION OF HALO ACETALS OF CYCLIC ALLYL ALCOHOLS AS A GENERAL ROUTE TO CONTROL VICINAL REGIO AND STEREOCHEMISTRYW
  157166. 1990 P. 675a
  157167. GABRIEL WEATHERHEAD
  157168. B&ADVANCES IN PHYSICAL ORGANIC CHEMISTRYC3RADICAL CAPTODATIVE REVIEW MESOMERIC STABLE SUSTMANM
  157169. 8345N
  157170. 2/28/96V
  157171. THE CAPTODATIVE EFFECTW
  157172. 1991a
  157173. GABRIEL WEATHERHEAD
  157174. ACCTS. CHEM. RES.CSDIELS ALDER CYCLOADDITION RATE HYDROPHOBIC EFFECT REVIEW AGGREGATE PRESSURE BRESLOWM
  157175. 8346N
  157176. 2/28/96V8HYDROPHOBIC EFFECTS ON SIMPLE ORGANIC REACTIONS IN WATERW
  157177. 1991 VOL. 24 P. 159a
  157178. GABRIEL WEATHERHEAD
  157179. JOCCmDIASTEREOSELECTIVE ALDOL CHIRAL ASYMMETRIC REVIEW STEREOCHEM BORON ENOLATE FELKIN ANH TRANSITION STATE ROUSCHM
  157180. 8347N
  157181. 2/28/96VhCONCERNING THE DIASTEROFACIAL SELECTIVITY OF THE ALDOL REACTIONS OF CHIRAL ALDEHYDES WITH BORON ENOLATESW
  157182. 1991 VOL. 56 PG. 4151a
  157183. GABRIEL WEATHERHEAD
  157184. JOCCmBENZENE SULFONYL ALLYL VINYL SULFONE WRITING INTRODUCTION CONDENSATION REVIEW DIELS ALDER PERICYCLIC HOFFMANNM
  157185. 8348N
  157186. 2/28/96V2SYNTHESIS AND REACTIONS OF METHYLENE KETO SULFONESW
  157187. 1991 VOL. 56 PG. 4098a
  157188. GABRIEL WEATHERHEAD
  157189. JOCCQJACOBSEN EPOXIDE ASYMMETRIC SYNTHESIS WRITING REVIEW EPOXIDATION CHIRAL INDUCTIONM
  157190. 8349N
  157191. 2/28/96VZASYMMETRIC OLEFIN EPOXIDATION WITH SODIUM HYPOCHLORITE CATALYZED BY CHIRAL SALEN COMPLEXESW
  157192. 1991 VOL. 56 PAGE 2296a
  157193. GABRIEL WEATHERHEAD
  157194. "B    SYNTHESISCASARKAR ALLYL SILANE ALLYLSILANE SILICON ALKENE REVIEW PREPARATIONM
  157195. 8350N
  157196. 2/28/96V4METHODS FOR THE SYNTHESIS OF ALLYLSILANES. TWO PARTSW
  157197. 1990 PAGE 969
  157198. GABRIEL WEATHERHEAD
  157199. NEW JOURN. CHEM.C:BACKVALL PALLADIUM ANNUALTION DIENE SULFONE REVIEW ACETATEM
  157200. 8351N
  157201. 2/28/96V=STEREOSELECTIVE ANNULATIONS VIA PALLADIUM CATALYZED REACTIONSW
  157202. 1990 VOL. 14 PAGE 447a
  157203. GABRIEL WEATHERHEAD
  157204. NEW JOURN. CHEM.C9DOETZ CARBENE FISCHER COMPLEX CYCLOADDITION REVIEW ALKYNEM
  157205. 8352N
  157206. 2/28/96V<CARBENE COMPLEXES IN STEREOSELECTIVE CYCLOADDITION REACTIONSW
  157207. 1990 VOL. 14 PAGE 433a
  157208. GABRIEL WEATHERHEAD
  157209. CHEM. SOC. REV.C(PAGE ACYL SILANE REVIEW SILICON CARBONYLM
  157210. 8353N
  157211. 2/28/96V'SYNTHESIS AND CHEMISTRY OF ACYL SILANESW
  157212. 1990 VOL. 19 PAGE 147a
  157213. GABRIEL WEATHERHEAD
  157214. Tet. Lett.CCSUSTMANN ENDO REVIEW INTRODUCTION DIELS ALDER FMO MO FAILURE THEORYM
  157215. 8354N
  157216. 2/28/96VNENDO/EXO SELECTIVITY IN CYCLOADDITIONS OF DIHYDROPYRIDINE WITH METHYL ACRYLATEW
  157217. 1991 PAGE 1401a
  157218. GABRIEL WEATHERHEAD
  157219. JOCCLWUEST EPOXIDE RING OPENING REVIEW CYCLOPROPANE TIN ELIMINATION EPOXY STANNES
  157220. 8355N
  157221. 2/28/96Va1,3 ELIMINATION REACTIONOS OF EPOXY BUTYL STANNANES. AN APPROACH TO CYCLOPROPYL CARBINYL ALCOHOLSW
  157222. 1991 VOL. 56 PAGE 2066a
  157223. GABRIEL WEATHERHEAD
  157224. ANG. CHEM. INT. ED. ENG.C,STODDART SYNTHESIS CYCLODEXTRIN REVIEW X RAYM
  157225. 8356N
  157226. 2/28/96V?SYNTHESIS AND CHARACTERIZATION OF PER 3,6 ANHYDRO CYCLODEXTRINSW
  157227. 1991 PAGE 80a
  157228. GABRIEL WEATHERHEAD
  157229. ANG. CHEM. INT. ED. ENG.CVNOYORI REVIEW ORGANOMETALLIC ENANTIOSELECTIVE MAGNESIUM ZINC LITHIUM ADDITION CARBONYLM
  157230. 8357N
  157231. 2/28/96V
  157232. ENANTIOSELECTIVE ADDITION OF ORGANOMETALLIC REAGENTS TO CARBONYL COMPOUNDS: CHIRALITY TRANSFER, MULTIPLICATION AND AMPLIFICATIONW
  157233. 1991 PAGE 49a
  157234. GABRIEL WEATHERHEAD
  157235. HELV. CHIM. ACTACQOBRECHT REVIEW REGIOSELECTIVITY ALKYNE DIENE DIHYDROPYRONE ALCOHOL INTRAMOLECULARM
  157236. 8358N
  157237. 2/28/96V
  157238. SYNTHESIS OF DIHYDROPYRANONES AND THEIR APPLICATION FOR THE IN SITU PREPARATION OF DIENES IN CARBONYL ALKYNE EXCHANGE WITH ACETYLENESW
  157239. 1991 PAGE 27a
  157240. GABRIEL WEATHERHEAD
  157241. +B    SYN. LETTCJGRIBBLE ALKALOID BENZYNE DIELS ALDER CANCER REVIEW OXIDATION ISOBENZOFURANM
  157242. 8359N
  157243. 2/28/96VUAPPROACHES TO THE SYNTHESIS OF THE PYRIDOCARBAZOLE ALKALOIDS USING ARYNES AND INDOLESW
  157244. 1991 PAGE 289a
  157245. GABRIEL WEATHERHEAD
  157246. ORG PREP PROCEDURE INTCUSUBSTITUTED FURANS CYCLO ADDITIONS DERIVATIVES ANNELATION ACETYLENES PRODUCTS PADWA AM
  157247. 8360N
  157248. 2/28/96V?RECENT DEVELOPMENTS IN THE AREA OF ANNULATED FURANS   A REVIEW.W
  157249. 1991 AUGX
  157250. 23(4)a
  157251. GABRIEL WEATHERHEAD
  157252. AUST J CHEMC
  157253. PYRROLIC COMPOUNDS OIL SHALE OXIDATIVE CYCLIZATION BILENES B RING SYSTEMS INTRAMOLECULAR CYCLIZATION SUBSTITUTED PORPHYRINS PROTOPORPHYRIN IX PROSTHETIC GROUP DIMETHYL ESTER CLEZY PSM
  157254. 8361N
  157255. 2/28/96VGSTUDIES IN PORPHYRIN CHEMISTRY   A SYNTHETIC APPROACH   INVITED REVIEW.W
  157256. 1991X    1163 1193Y
  157257. 44(9)a
  157258. GABRIEL WEATHERHEAD
  157259. ORG PREP PROCEDURE INT
  157260. 1,3 DIPOLAR CYCLO ADDITION ANTIBACTERIAL AGENTS AZOMETHINE IMINES ELECTROCHEMICAL OXIDATION BICYCLIC PYRAZOLIDINONES STRETCHING VIBRATION THERMIC BEHAVIOR POLAR COMPOUNDS PYRAZOLIDONE (3) AZOMETHINEIMINES 1 PHENYLPYRAZOLIDIN 3 ONES CLARAMUNT RMM
  157261. 8362N
  157262. 2/28/96V,THE CHEMISTRY OF PYRAZOLIDINONES   A REVIEW.W
  157263. 1991 JUNX
  157264. 273 320Y
  157265. 23(3)a
  157266. GABRIEL WEATHERHEAD
  157267. 8363N
  157268. 2/28/96VxA REVIEW. WEBER, W. P. SILICON REAGENTS FOR ORGANIC SYNTHESIS (CONCEPTS IN ORGANIC CHEMISTRY, VOL. 14). SPRINGER VERLAG:a
  157269. GABRIEL WEATHERHEAD
  157270. 8364N
  157271. 2/28/96VkA REVIEW. UGO, R., ED. ASPECTS OF HOMOGENEOUS CATALYSIS, VOL. 4. D. REIDEL PUBLISHING CO.: DORDRECHT, 1981.a
  157272. GABRIEL WEATHERHEAD
  157273. 8365N
  157274. 2/28/96V
  157275. A REVIEW. PIZEY, J. S., ED. SYNTHETIC REAGENTS, VOL. 4. MERCURIC ACETATE, PERIODIC ACID AND SULFURYL CHLORIDE. BLLIS HORWOOD, LTD., CHICHESTER AND WILEY: NEW YORK, 1981.a
  157276. GABRIEL WEATHERHEAD
  157277. 8366N
  157278. 2/28/96
  157279. A REVIEW. MURRAY, JR., R. D. H.; MENDEZ, J.; BROWN, S. A. THE NATURAL COUMARINS: OCCURRENCE, CHEMISTRY AND BIOCHEMISTRY. WILEY INTERSCIENCE: NEW YORK, 1982.a
  157280. GABRIEL WEATHERHEAD
  157281. 8367N
  157282. 2/28/96V^A REVIEW. MUCCINO, R. R. ORGANIC SYNTHESIS WITH CARBON 14. WILEY INTERSCIENCE: NEW YORK, 1982.a
  157283. GABRIEL WEATHERHEAD
  157284. 8368N
  157285. 2/28/96VZA REVIEW. KLUMPP, G. REACTIVITY IN ORGANIC CHEMISTRY.  WILEY INTERSCIENCE: NEW YORK, 1982.a
  157286. GABRIEL WEATHERHEAD
  157287. 8369N
  157288. 2/28/96V
  157289. A REVIEW. KIRBY, A. J. THE ANOMERIC EFFECT AND RELATED STEREOELECTRONIC EFFECTS AT OXYGEN (CONCEPTS IN ORGANIC CHEMISTRY, VOL. 12), SPRINGER VERLAG: NEW YORK, 1982.a
  157290. GABRIEL WEATHERHEAD
  157291. 8370N
  157292. 2/28/96VhA REVIEW. KENNEDY, J. P.; MARECHAL, E. CARBOCATIONIC POLYMERIZATION. WILEY INTERSCIENCE: NEW YORK, 1981.a
  157293. GABRIEL WEATHERHEAD
  157294. 8371N
  157295. 2/28/96
  157296. A REVIEW. GOKEL, G. W.; KORZENIOWSKI, S. H. MACROCYCLIC POLYETHER SYNTHESES (CONCEPTS IN ORGANIC CHEMISTRY, VOL. 13). SPRINGER VERLAG: NEW YORK, 1982.a
  157297. GABRIEL WEATHERHEAD
  157298. 8372N
  157299. 2/28/96VUA REVIEW. ERSHOV, V. V.; NIKIFOROV, G. A. QUINONE DIAZIDES. ELSEVIER: NEW YORK, 1981.a
  157300. GABRIEL WEATHERHEAD
  157301. 8373N
  157302. 2/28/96V
  157303. A REVIEW. DEJONG, F.; REINHOUDT, D. N. STABILITY AND REACTIVITY OF CROWN ETHER COMPLEXES. ACADEMIC PRESS, INC.: NEW YORK, 1981.a
  157304. GABRIEL WEATHERHEAD
  157305. 8374N
  157306. 2/28/96V|A REVIEW. BARLIN, GORDON B. THE PYRAZINES, CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 41. WILEY INTERSCIENCE: NEW YORK, 1982.a
  157307. GABRIEL WEATHERHEAD
  157308. 8375N
  157309. 2/28/96V
  157310. A REVIEW. SAEGUSA, T. NEW DEVELOPMENTS IN POLYMER SYNTHESIS. 982, 100, 75. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157311. GABRIEL WEATHERHEAD
  157312. 8376N
  157313. 2/28/96
  157314. A REVIEW. ZIMMERMAN, H. E. TOPICS IN PHOTOCHEMISTRY. 1982 00, 45. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157315. GABRIEL WEATHERHEAD
  157316. 8377N
  157317. 2/28/96V
  157318. A REVIEW. ANDERS, E.; HAYATSU, R. ORGANIC COMPOUNDS IN METERORITES AND THEIR ORIGINS. 1981, 99,1. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157319. GABRIEL WEATHERHEAD
  157320. 8378N
  157321. 2/28/96V
  157322. A REVIEW. ADAM, W.; BLOODWORTH, A. J. CHEMISTRY OF SATURATED BICYCLIC PEROXIDES
  157323. THE PROSTAGLANDIN CONNECTION. 1981, 97, 121. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157324. GABRIEL WEATHERHEAD
  157325. 8379N
  157326. 2/28/96V
  157327. A REVIEW. REGITZ, M.; MAAS, G. SHORT LIVED PHOSPHORUS(V) COMPOUNDS HAVING COORDINATION NUMBER 3. 1981, 97, 71. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157328. GABRIEL WEATHERHEAD
  157329. 8380N
  157330. 2/28/96V
  157331. A REVIEW. MURATA, L; NAKASUKI, K. RECENT ADVANCES IN THIEPIN CHEMISTRY. 1981, 97, 33. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157332. GABRIEL WEATHERHEAD
  157333. 8381N
  157334. 2/28/96V
  157335. A REVIEW. SCHWARZ, H. RADICAL ELIMINATIONS FROM GASEOUS CATION RADICALS VIA MULTISTEP PATHWAYS
  157336. THE CONCEPT OF  HIDDEN  HYDROGEN REARRANGEMENTS. 1981, 97,1. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1981 AND 982.a
  157337. GABRIEL WEATHERHEAD
  157338. 8382N
  157339. 2/28/96V
  157340. A REVIEW. MARKO, L.; MARKO MONOSTORY, B. COMPLEXES WITH SULPHUR CONTAINING LIGANDS, P 283. THE ORGANIC CHEMISTRY OF IRON, VOL. 2 E. A. K. VON GUSTORF, F. W. GREVELS, AND 1. FISCHLER, EDS. ACADEMIC PRESS: NEW YORK, 1981.a
  157341. GABRIEL WEATHERHEAD
  157342. 8383N
  157343. 2/28/96
  157344. A REVIEW. CHINI, P. COMPOUNDS WITH IRON METAL BONDS AND CLUSTERS, P 189. THE ORGANIC CHEMISTRY OF IRON, VOL. 2 E. A. K. VON GUSTORF, F. W. GREVELS, AND 1. FISCHLER, EDS. ACADEMIC PRESS: NEW YORK, 1981.a
  157345. GABRIEL WEATHERHEAD
  157346. 8384N
  157347. 2/28/96V
  157348. A REVIEW. KING, R. B. ARENE COMPLEXES, P 155. THE ORGANIC CHEMISTRY OF IRON, VOL. 2 E. A. K. VON GUSTORF, F. W. GREVELS, AND 1. FISCHLER, EDS. ACADEMIC PRESS: NEW YORK, 1981.a
  157349. GABRIEL WEATHERHEAD
  157350. 8385N
  157351. 2/28/96V
  157352. A REVIEW. KERBER, R. C. IRON COMPLEXES OF TRIENES, TETRAENES AND POLYENES, P 1. THE ORGANIC CHEMISTRY OF IRON, VOL. 2 E. A. K. VON GUSTORF, F. W. GREVELS, AND 1. FISCHLER, EDS. ACADEMIC PRESS: NEW YORK, 1981.a
  157353. GABRIEL WEATHERHEAD
  157354. 8386N
  157355. 2/28/96V
  157356. A REVIEW. MCGRATH, J. E.; RIFFLE, J. S. POLYMERIZATION OF CYCLOSILOXANES, P 62. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157357. GABRIEL WEATHERHEAD
  157358. 8387N
  157359. 2/28/96
  157360. A REVIEW. ARKLES, B. TECHNIQUES FOR SILYLATION P 56 SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157361. GABRIEL WEATHERHEAD
  157362. 8388N
  157363. 2/28/96V
  157364. A REVIEW. WEST, R. ORGANOPOLYSILANES, P 46. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157365. GABRIEL WEATHERHEAD
  157366. 8389N
  157367. 2/28/96V
  157368. A REVIEW. KOGA, I. REDUCTIONS USING HYDROSILANES, P 36. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157369. GABRIEL WEATHERHEAD
  157370. 8390N
  157371. 2/28/96V
  157372. A REVIEW. BARTON, T. J. REACTIVE INTERMEDIATES IN ORGANOSILICON CHEMISTRY, P 26. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157373. GABRIEL WEATHERHEAD
  157374. 8391N
  157375. 2/28/96
  157376. A REVIEW. HUDRLIK, P. F.; HURDLIK, A. M. ORGANOSILICON COMPOUNDS IN ORGANIC SYNTHESIS, P 14. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157377. GABRIEL WEATHERHEAD
  157378. 8392N
  157379. 2/28/96V
  157380. A REVIEW. WASHBURNE, S. S. AN ORGANOSILICON PRIMER, P 8. SILICON COMPOUNDS. REGISTER AND REVIEW, S. S. PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1982.a
  157381. GABRIEL WEATHERHEAD
  157382. 8393N
  157383. 2/28/96V
  157384. A REVIEW. UGI, I.; MARQUARDING, D.; URBAN, R. THE SYNTHESIS OF PEPTIDES BY FOUR COMPONENT CONDENSATION. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157385. GABRIEL WEATHERHEAD
  157386. 8394N
  157387. 2/28/96V
  157388. A REVIEW. CHILTON, W. S. SECONDARY AMINO ACIDS OF MUSHROOMS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157389. GABRIEL WEATHERHEAD
  157390. 8395N
  157391. 2/28/96
  157392. A REVIEW. BENEDETTI, E. STRUCTURE AND CONFORMATION OF PEPTIDES AS DETERMINED BY X RAY CRYSTALLOGRAPHY. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157393. GABRIEL WEATHERHEAD
  157394. 8396N
  157395. 2/28/96V
  157396. A REVIEW. PICKART, L. PEPTIDE AND PROTEIN COMPLEXES OF TRANSITION METALS AS MODULATORS OF CELL GROWTH. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157397. GABRIEL WEATHERHEAD
  157398. 8397N
  157399. 2/28/96V
  157400. A REVIEW. STAMMER, C. H. DEHYDROAMINO ACIDS AND PROTEINS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157401. GABRIEL WEATHERHEAD
  157402. 8398N
  157403. 2/28/96
  157404. A REVIEW. HILL, W. E. RIBOSOMAL PROTEIN SYNTHESIS AND STRUCTURE. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 6, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1982.a
  157405. GABRIEL WEATHERHEAD
  157406. 8399N
  157407. 2/28/96V
  157408. A REVIEW. DOPKE, W. THE EBURNAMINE VINCAMINE ALKALOIDS. THE ALKALOIDS, R. G. A. RODRIGO, ED., VOL. 20, ACADEMIC PRESS: NEW YORK, 1982.a
  157409. GABRIEL WEATHERHEAD
  157410. 8400N
  157411. 2/28/96VxA REVIEW. SAXTON, E. BISINDOLE ALKALOIDS. THE ALKALOIDS, R. G. A. RODRIGO, ED., VOL. 20, ACADEMIC PRESS: NEW YORK, 1982.a
  157412. GABRIEL WEATHERHEAD
  157413. 8401N
  157414. 2/28/96VoA REVIEW. MIKOLAJCZYK, M. DRABOWICZ, J. CHIRAL ORGANOSULFUR COMPOUNDS. 1982, 13, 333. TOPICS IN STEREOCHEMISTRYa
  157415. GABRIEL WEATHERHEAD
  157416. 8402N
  157417. 2/28/96VmA REVIEW. MIKOLAJCZYK, M.; DRABOWICA, J. NMR CHIRAL SOLVATING AGENTS. 1982,13, 263. TOPICS IN STEREOCHEMISTRYa
  157418. GABRIEL WEATHERHEAD
  157419. 8403N
  157420. 2/28/96
  157421. WVyA REVIEW. STEWART, M.; ARNETT, E. M. CHIRAL MONOLAYERS AT THE AIR WATER INTERFACE. 1982,13,195. TOPICS IN STEREOCHEMISTRYa
  157422. GABRIEL WEATHERHEAD
  157423. 8404N
  157424. 2/28/96V
  157425. A REVIEW. OSAWA, E.; MUSSO, H. APPLICATIONS OF MOLECULAR MECHANICS CALCULATIONS TO ORGANIC CHEMISTRY. 1982,13,117. TOPICS IN STEREOCHEMISTRYa
  157426. GABRIEL WEATHERHEAD
  157427. 8405N
  157428. 2/28/96V~A REVIEW. EVANS, D. A.; NELSON, J. V.; TABER, T. R. STEREOSELECTIVE ALDOL CONDENSATIONS. 1982,13, 1. TOPICS IN STEREOCHEMISTRYa
  157429. GABRIEL WEATHERHEAD
  157430. 8406N
  157431. 2/28/96VZA REVIEW. LAROCK, R. C. ORGANOMERCURIALS IN ORGANIC SYNTHESIS. 1982, 38, 1713. TETRAHEDRONa
  157432. GABRIEL WEATHERHEAD
  157433. 8407N
  157434. 2/28/96VfA REVIEW. FREY, P. A. STEREOCHEMISTRY OF ENZYMATIC REACTIONS OF PHOSPHATES. 1982, 38,1541. TETRAHEDRONa
  157435. GABRIEL WEATHERHEAD
  157436. 8408N
  157437. 2/28/96
  157438. A REVIEW. ALBRIGHT, T. A. STRUCTURE AND REACTIVITY IN ORGANOMETALLIC CHEMISTRY. AN APPLIED MOLECULAR ORBITAL APPROACH. 1982, 38,1339. TETRAHEDRONa
  157439. GABRIEL WEATHERHEAD
  157440. 8409N
  157441. 2/28/96V
  157442. A REVIEW. WOOD, G. W. SOME RECENT APPLICATION OF FIELD IONIZATION/FIELD DESORPTION MASS SPECTROMETRY TO ORGANIC CHEMISTRY. 1982, 38, 1125. TETRAHEDRONa
  157443. GABRIEL WEATHERHEAD
  157444. 8410N
  157445. 2/28/96VgA REVIEW. WALSH, C. SUICIDE SUBSTRATES: MECHANISM BASED ENZYME INACTIVATORS. 1982, 38, 871. TETRAHEDRONa
  157446. GABRIEL WEATHERHEAD
  157447. 8411N
  157448. 2/28/96VQA REVIEW. CHILDS,R.F. CIRCUMAMBULATORY REARRANGEMENTS. 1982, 38, 567. TETRAHEDRONa
  157449. GABRIEL WEATHERHEAD
  157450. 8412N
  157451. 2/28/96V?A REVIEW. REINECKE, M. G. HETARYNES. 1982, 38, 427. TETRAHEDRONa
  157452. GABRIEL WEATHERHEAD
  157453. 8413N
  157454. 2/28/96
  157455. A REVIEW. TEDDER, J. M. THE IMPORTANCE OF POLARITY, BOND STRENGTH AND STERIC EFFECTS IN DETERMINING THE SITE ATTACK AND THE RATE OF FREE RADICAL SUBSTITUTION IN ALIPHATIC COMPOUNDS. 1982, 38, 313. TETRAHEDRONa
  157456. GABRIEL WEATHERHEAD
  157457. 8414N
  157458. 2/28/96VyA REVIEW. LOUNASMAA, M. NEMES, A. THE SYNTHESIS OF BIS INDOLE ALKALOIDS AND THEIR DERIVATIVES. 1982, 38, 223. TETRAHEDRONa
  157459. GABRIEL WEATHERHEAD
  157460. 8415N
  157461. 2/28/96V
  157462. A REVIEW. GAWRONSKI, J. K. CIRCULAR DICHROISM AND STEREOCHEMISTRY OF CHIRAL CONJUGATED CYCLOHEXENONES. 1982, 38, 3. TETRAHEDRONa
  157463. GABRIEL WEATHERHEAD
  157464. 8416N
  157465. 2/28/96V
  157466. A REVIEW. ARBUZOV, B. A., ZOBOVA, N. N. ADDITION OF ALIPHATIC AND AROMATIC ACYL ISOCYANATES TO UNSATURATED COMPOUNDS. 1982, 433. SYNTHESISa
  157467. GABRIEL WEATHERHEAD
  157468. 8417N
  157469. 2/28/96V
  157470. A REVIEW. DARBARWAR, M.; SUNDARAMEURTHY, V. SYNTHESIS OF COUMARINS WITH 3:4 FUSED RING SYSTEMS AND THEIR PHYSIOLOGICAL ACTIVITY. 1982, 337. SYNTHESIS
  157471. GABRIEL WEATHERHEAD
  157472. 8418N
  157473. 2/28/96V
  157474. A REVIEW. PIANCATELLI, G.; SCETTRI, A.; D'AURIA, M. PYRIDINIUM CHLOROCHROMATE: A VERSATILE OXIDANT IN ORGANIC SYNTHESIS. 1982, 245. SYNTHESISa
  157475. GABRIEL WEATHERHEAD
  157476. 8419N
  157477. 2/28/96VXA REVIEW. KOBER, F. AMINOARSANES AS PREPARATIVE REAGENTS (IN GER.). 1982, 173. SYNTHESISa
  157478. GABRIEL WEATHERHEAD
  157479. 8420N
  157480. 2/28/96V
  157481. A REVIEW. STANG, P. J., HANACK, M., SUBRAMANIAN, L. R. PERFLUOROALKANESULFONIC ESTERS: METHODS OF PREPARATION AND APPLICATIONS IN ORGANIC CHEMISTRY. 1982, 85. SYNTHESISa
  157482. GABRIEL WEATHERHEAD
  157483. 8421N
  157484. 2/28/96
  157485. 'A REVIEW. EMDE, H.; DOMSCH, D.; FEGER, H.; FRICK, U.; GOTZ, A.; HERGOTT, H. H., HOFMANN, K.; KOBER, W.; KRAGELOB, K.; OESTERLE, T.; STEPPAN, W.; WEST, W.; SIMCHEN, G. TRIALKYLSILYL PERFLUOROALKANESULFONATES: HIGHLY REACTIVE SILYLATING AGENTS AND LEWIS ACIDS IN ORGANIC SYNTHESIS. 1982, SYNTHESIS
  157486. GABRIEL WEATHERHEAD
  157487. 8422N
  157488. 2/28/96V
  157489. A REVIEW. KORSHAK, V. V.; RUSANOV, A. L.; TUGUSHI, D. S. REDUCTIVE POLYHETEROCYCLISATION
  157490. NEW METHOD OF PREPARATION OF POLYHETEROARYLENES. 1981, 50, 1177. RUSSIAN CHEMICAL REVIEWSa
  157491. GABRIEL WEATHERHEAD
  157492. 8423N
  157493. 2/28/96V
  157494. A REVIEW. VAREZHKIN, YU. M.; ZHINKIN, D. YA.; MORGUNOVA, M. M. THE STRUCTURE AND PROPERTIES OF ORGANOCYCLODISILAZANES. 1981, 50, 1158. RUSSIAN CHEMICAL REVIEWSa
  157495. GABRIEL WEATHERHEAD
  157496. 8424N
  157497. 2/28/96V
  157498. A REVIEW. MNDZHOYAN, 0. L.; TOPUZYAN, V. 0. METHODS OF SYNTHESIS AND PROPERTIES OF B DIMETHYLAMINOETHYL AND CHOLINE ESTERS OF AMINOACIDS AND PEPTIDES. 1981, 50, 1151.RUSSIAN CHEMICAL REVIEWSa
  157499. GABRIEL WEATHERHEAD
  157500. 8425N
  157501. 2/28/96V
  157502. A REVIEW. BABICHEV, F. S.; KOVTUNENKO, V. A.; TYLTIN, A. K. ADVANCES IN THE CHEMISTRY OF ISOINDOLE. 1981, 50,1087. RUSSIAN CHEMICAL REVIEWSa
  157503. GABRIEL WEATHERHEAD
  157504. 8426N
  157505. 2/28/96
  157506. A REVIEW. BADANYAN, SH. 0.; VOSKANYAN, M. G.; CHOBANYAN, ZH. A. COPPER SALTS IN CATALYTIC REACTIONS OF ORGANIC COMPOUNDS. 1981, 50, 1074. RUSSIAN CHEMICAL REVIEWSa
  157507. GABRIEL WEATHERHEAD
  157508. 8427N
  157509. 2/28/96V
  157510. A REVIEW. BRAGIN, O. V. CATALYTIC CYCLO OLIGOMERISATION REACTIONS OF LOWER OLEFINS AND ALKANES WITH FORMATION OF AROMATIC HYDROCARBONS. 1981, 50, 1045. RUSSIAN CHEMICAL REVIEWSa
  157511. GABRIEL WEATHERHEAD
  157512. 8428N
  157513. 2/28/96VkA REVIEW. KARNOJITZKY, V. OXIDATION OF KETONES BY MOLECULAR OXYGEN. 1981, 50, 888. RUSSIAN CHEMICAL REVIEWSa
  157514. GABRIEL WEATHERHEAD
  157515. 8429N
  157516. 2/28/96VzA REVIEW. GAMAYUROVA, V. S. THE BASICITY AND NUCLEOPHILICITY OF ARSENYL COMPOUNDS. 1981, 50, 836. RUSSIAN CHEMICAL REVIEWSa
  157517. GABRIEL WEATHERHEAD
  157518. 8430N
  157519. 2/28/96VgA REVIEW. POZHARSKII, A. F.; DAL'NIKOVSKAYA, V. V. PERIMIDINES. 1981, 50, 816. RUSSIAN CHEMICAL REVIEWSa
  157520. GABRIEL WEATHERHEAD
  157521. 8431N
  157522. 2/28/96
  157523. sV~A REVIEW. FURMANOVA, N. G. THE CRYSTAL STRUCTURES OF POTENTIALLY TAUTOMERIC COMPOUNDS. 1981, 50, 775. RUSSIAN CHEMICAL REVIEWSa
  157524. GABRIEL WEATHERHEAD
  157525. 8432N
  157526. 2/28/96V
  157527. A REVIEW. RAKHMANKULOV, D. L.; ZLOTSKII, S. S.; ZORIN, V. V., IMASHEV, U. B.; KARAKHANOV, R. A. RADICAL CHAIN REACTIONS OF ACETALS IN SOLUTION. 1981, 50, 762. RUSSIAN CHEMICAL REVIEWSa
  157528. GABRIEL WEATHERHEAD
  157529. 8433N
  157530. 2/28/96VdA REVIEW. SHTEINGARTS, V. D. POLYFLUORINATED ARENONIUM IONS. 1981, 50, 735. RUSSIAN CHEMICAL REVIEWSa
  157531. GABRIEL WEATHERHEAD
  157532. 8434N
  157533. 2/28/96VuA REVIEW. MARTINEK, K.; SEMENOV, A. N. ENZYME CATALYSIS IN ORGANIC SYNTHESIS. 1981, 50, 718. RUSSIAN CHEMICAL REVIEWSa
  157534. GABRIEL WEATHERHEAD
  157535. 8435N
  157536. 2/28/96V
  157537. A REVIEW. FEDOROV, L. A.; KRAVTSOV, D. N.; PEREGUDOV, A. S. METALLOTROPIC TAUTOMERIC TRANSFORMATIONS OF THE S,S TYPE IN ORGANOMETALLIC AND COMPLEX COMPOUNDS. 1981, 50, 682. RUSSIAN CHEMICAL REVIEWSa
  157538. GABRIEL WEATHERHEAD
  157539. 8436N
  157540. 2/28/96VzA REVIEW. MIRONOV, V. A.; FEDOROVICH, A. D.; AKHREM, A. A. THE 1,5 SHIFT REACTION. 1981, 50, 666. RUSSIAN CHEMICAL REVIEWSa
  157541. GABRIEL WEATHERHEAD
  157542. 8437N
  157543. 2/28/96V
  157544. A REVIEW. MARETINA, I. A.; TSIL'KO, A. E.; ZAICHENKO, YU. A. THE SYNTHESIS OF HETEROCYCLES FROM VINYLACETYLENES OR DIACETYLENES AND NITROGEN CONTAINING DINUCLEOPHILES. 1981, 50, 657. RUSSIAN CHEMICAL REVIEWSa
  157545. GABRIEL WEATHERHEAD
  157546. 8438N
  157547. 2/28/96V
  157548. A REVIEW. ODINOKOV, V. N.; TOLSTIKOV, G. A. OZONOLYSIS
  157549. A MODERN METHOD IN THE CHEMISTRY OF OLEFINS. 1981, 50, 636. RUSSIAN CHEMICAL REVIEWSa
  157550. GABRIEL WEATHERHEAD
  157551. 8439N
  157552. 2/28/96V
  157553. A REVIEW. YAKHONTOV, L. N.; KRASNOKUTSKAYA, D. M. ADVANCES IN THE CHEMISTRY OF A,A' DISUBSTITUTED PYRIDINES. 1981, 50, 565. RUSSIAN CHEMICAL REVIEWSa
  157554. GABRIEL WEATHERHEAD
  157555. 8440N
  157556. 2/28/96
  157557. |VwA REVIEW. SHCHEGOLEV, A. A.; KANISHCHEV, M. I. REARRANGEMENTS IN VINYL CATIONS. 1981, 50, 553. RUSSIAN CHEMICAL REVIEWSa
  157558. GABRIEL WEATHERHEAD
  157559. 8441N
  157560. 2/28/96V
  157561. A REVIEW. BELETSKAYA, I. P., MAKHON'KOV, D. I. OXIDATION OF ALKYL DERIVATIVES OF AROMATIC HYDROCARBONS BY TRANSITION METAL SALTS. 1981, 50, 534. RUSSIAN CHEMICAL REVIEWSa
  157562. GABRIEL WEATHERHEAD
  157563. 8442N
  157564. 2/28/96V
  157565. A REVIEW. BUCK H.M. SPECTROPHYSICS AND PHOTOCHEMISTRY OFTHE FORMALDEHYDE MOLECULE. PART I. 1982,101,193. RECUEIL: JOURNAL ROYAL NETHERLANDS CHEMICAL SOCIETYa
  157566. GABRIEL WEATHERHEAD
  157567. 8443N
  157568. 2/28/96V
  157569. A REVIEW. STEGGERDA, J. J.; BOUR, J. J.; VAN DER VELDEN, J. W. A.  PREPARATION AND PROPERTIES OF GOLD CLUSTER COMPOUNDS. 1982, 101, 164. RECUEIL: JOURNAL ROYAL NETHERLANDS CHEMICAL SOCIETYa
  157570. GABRIEL WEATHERHEAD
  157571. 8444N
  157572. 2/28/96VtA REVIEW. ZWANENBURG, B. THE CHEMISTRY OF SULFINES. 1982, 101, 1 RECUEIL: JOURNAL ROYAL NETHERLANDS CHEMICAL SOCIETY
  157573. GABRIEL WEATHERHEAD
  157574. 8445N
  157575. 2/28/96ViA REVIEW. HECK, R. F. PALLADIUM CATALYZED VINYLATION OF ORGANIC HALIDES. 1982, 27, 345. ORGANIC REACTIONSa
  157576. GABRIEL WEATHERHEAD
  157577. 8446N
  157578. 2/28/96V
  157579. A REVIEW. BIELLMANN, J. F.; DUCEP, J. B. ALLYLIC AND BENZYLIC CARBANIONS SUBSTITUTED BY HETEROATOMS. 1982, 27,1. ORGANIC REACTIONSa
  157580. GABRIEL WEATHERHEAD
  157581. 8447N
  157582. 2/28/96VyA REVIEW. WALLACE, R. G. HYDROXYLAMINE O SULPHONIC ACID. 1982, 14, 265. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  157583. GABRIEL WEATHERHEAD
  157584. 8448N
  157585. 2/28/96V
  157586. A REVIEW. OSHRY, L.; ROSENFELD, S. M. SYNTHESIS AND USES OF B KETO ACIDS. 1982,14, 249. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  157587. GABRIEL WEATHERHEAD
  157588. 8449N
  157589. 2/28/96V}A REVIEW. SUCROW, W. REACTIONS OF ACETYLENES WITH HYDRAZINES. 1982, 14, 91. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  157590. GABRIEL WEATHERHEAD
  157591. 8450N
  157592. 2/28/96
  157593. A REVIEW. DRABOWICZ, J.; MIKOLAJCZYK, M. SYNTHESIS OF SULFOXIDES. 1982, 14, 45. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  157594. GABRIEL WEATHERHEAD
  157595. 8451N
  157596. 2/28/96V
  157597. A REVIEW. JOLLEY, S. T.; BRADSHAW, J. S.; IZATT, R. M. SYNTHETIC CHIRAL MACROCYCLIC CROWN LIGANDS. 1982,19, 3. JOURNAL OF HETEROCYCLIC CHEMISTRYa
  157598. GABRIEL WEATHERHEAD
  157599. 8452N
  157600. 2/28/96V
  157601. A REVIEW. CATSOULACOS, P.; CAMOUTSIS, C. STEROIDAL THIAZOLES, ISOTHIAZOLES, THIAZOLINES, AND THIAZOLIDINES. 1981,18,1485. JOURNAL OF HETEROCYCLIC CHEMISTRYa
  157602. GABRIEL WEATHERHEAD
  157603. 8453N
  157604. 2/28/96V
  157605. A REVIEW. BARBER, J.; NAKATANI, H. Y.; MANSFIELD, R. PHOTOSYNTHETIC OXYGEN EVOLUTION AND THE WATER SPLITTING ENZYME. 1981, 21,243 ISRAEL JOURNAL OF CHEMISTRYa
  157606. GABRIEL WEATHERHEAD
  157607. 8454N
  157608. 2/28/96VuA REVIEW. AFZAL, M.; AL ORIQUAT, G. BIOSYNTHESIS OF ISOFLAVONOID AND RELATED PHYTOALEXINS. 1982,19,1295. HETEROCYCLESa
  157609. GABRIEL WEATHERHEAD
  157610. 8455N
  157611. 2/28/96V
  157612. A REVIEW. SARAF, S.; KHAN, M. A.; AL MOUSAWI, S. PROTON MAGNETIC RESONANCE OF PHENOTHIAZINE DERIVATIVES. 1982,19,1148. HETEROCYCLESa
  157613. GABRIEL WEATHERHEAD
  157614. 8456N
  157615. 2/28/96V
  157616. A REVIEW. FRIEDRICHSEN, W.; KAPPE, T.; BOTTCHER, A. SIX MEMBERED MESOIONIC HETEROCYCLES ON THE M QUINODIMETHANE DIANION TYPE. 1982,19, 1083. HETEROCYCLESa
  157617. GABRIEL WEATHERHEAD
  157618. 8457N
  157619. 2/28/96VqA REVIEW. SARAF, S.; KHAN, M. A.; AL MOUSAWI, S. ABSORPTION SPECTRA OF PHENOTHIAZINES. 1982,19, 935. HETEROCYCLESa
  157620. GABRIEL WEATHERHEAD
  157621. 8458N
  157622. 2/28/96V
  157623. A REVIEW. RAMADA, S. R.; CHENCHAIAH, P. C., CHANDRA KUMAR, N. S.; KRISHNA, M. V.; SRINIVAS, P. S.; KAMESWARA SASTRY, V. V. S.; RAO, J. A. A REVIEW ON THE PARTIAL AND TOTAL SYNTHESES OF THIASTEROIDS. 1982,19, 861. HETEROCYCLESa
  157624. GABRIEL WEATHERHEAD
  157625. 8459N
  157626. 2/28/96
  157627. A REVIEW. BREMNER, J. B.; BROWNE, E. J.; GUNAWARDANA, I. W. K. OXAZA AND DIOXAZA MEDIUM SIZED HETEROCYCLES AND BENZ FUSED DERIVATIVES. 1982,19, 709. HETEROCYCLESa
  157628. GABRIEL WEATHERHEAD
  157629. 8460N
  157630. 2/28/96VwA REVIEW. ELNAGDI, M. H.; ZAYED, E. M.; ABDOU, S. CHEMISTRY OF HETEROCYCLIC DIAZO COMPOUNDS. 1982,19, 559. HETEROCYCLESa
  157631. GABRIEL WEATHERHEAD
  157632. 8461N
  157633. 2/28/96VvA REVIEW. WOZNIAK, M.; VAN DER PLAS, H. C. ADVANCES IN THE CHEMISTRY OF 1,7 NAPHTHYRIDINES. 1982,19, 363. HETEROCYCLESa
  157634. GABRIEL WEATHERHEAD
  157635. 8462N
  157636. 2/28/96VpA REVIEW. BLENDERMAN, W. G.; JOULLIE, M. M. SYNTHETIC APPROACHES TO DIHYDROTHIOPHENES. 1982,19,111. HETEROCYCLESa
  157637. GABRIEL WEATHERHEAD
  157638. 8463N
  157639. 2/28/96V
  157640. A REVIEW.  PAUDLER, W. W., JOVANOVIC, M. V. BACKDONATION AND IRRELATIONSHIPS BETWEEN 15N, 13C CHEMICAL SHIFTS AND INFRARED ABSORPTION FREQUENCIES IN HETEROCYCLIC N OXIDES. 1982, 19, 93. HETEROCYCLESa
  157641. GABRIEL WEATHERHEAD
  157642. 8464N
  157643. 2/28/96V~A REVIEW. DAHLHOFF, W. V.; KOSTER, R. SOME NEW O ETHYLBORON ASSISTED CARBOHYDRATE TRANSFORMATIONS. 1982, 18, 421. HETEROCYCLESa
  157644. GABRIEL WEATHERHEAD
  157645. 8465N
  157646. 2/28/96VXA REVIEW. KANNER, B. 2,6 DI T BUTYLPYRIDINE
  157647. AN UNUSUAL BASE. 1982, 18, 411. HETEROCYCLESa
  157648. GABRIEL WEATHERHEAD
  157649. 8466N
  157650. 2/28/96VaA REVIEW. LAROCK, R. C. NEW ORGANOMETALLIC APPROACHES TO HETEROCYCLES. 1982,18, 397. HETEROCYCLESa
  157651. GABRIEL WEATHERHEAD
  157652. 8467N
  157653. 2/28/96V
  157654. A REVIEW.  SINGARAM, B.; PAI, G. G. ADDITION COMPOUNDS OF BORON TRIFLUORIDE, BORANES, AND ALANE WITH N,N,N',N' TETRAMETHYLETHYLENEDIAMINE AND TRIETHYLENEDIAMINE. 1982,18, 387. HETEROCYCLESa
  157655. GABRIEL WEATHERHEAD
  157656. 8468N
  157657. 2/28/96V
  157658. A REVIEW. YAMAMOTO, Y.; MARUYAMA, K. ORGANOMETALLIC COMPOUNDS FOR STEREOREGULATED SYNTHESIS OF ACYLIC SYSTEMS. THEIR APPLICATION TO THE SYNTHESIS OF THE PRELOG DJERASSI LACTONIC ACID. 1982,18, 357. HETEROCYCLESa
  157659. GABRIEL WEATHERHEAD
  157660. 8469N
  157661. 2/28/96V
  157662. A REVIEW. TRUCE, W. E.; DEAN, B. D. CYCLOADDUCTS DERIVED FROM SULFENES OR KETENES AND TROPONE OR ANALOGS OF TROPONE. 1982, 18, 343. HETEROCYCLESa
  157663. GABRIEL WEATHERHEAD
  157664. 8470N
  157665. 2/28/96V
  157666. A REVIEW. MIZUNO, Y.; ITOH, T.; NOMURA, A. AZANUCLEOSIDES AND DEAZANUCLEOSIDES OF BIOLOGICAL INTEREST. 1982,17, 615. HETEROCYCLESa
  157667. GABRIEL WEATHERHEAD
  157668. 8471N
  157669. 2/28/96V
  157670. A REVIEW. CHU, Y. L.; CHU, J. H. STUDIES ON THE DITERPENE ALKALOIDS OF THE CHINESE DRUGE, ACONITUM SPP. 1982 17, 607. HETEROCYCLESa
  157671. GABRIEL WEATHERHEAD
  157672. 8472N
  157673. 2/28/96V
  157674. A REVIEW. WASSERMAN, H. H.; WU, J. S. THE TOTAL SYNTHESIS OF MACROCYCLIC SPERMINE AND SPERMIDINE ALKALOIDS. 1982,17, 581. HETEROCYCLESa
  157675. GABRIEL WEATHERHEAD
  157676. 8473N
  157677. 2/28/96
  157678. A REVIEW. SETO, H.; OTAKE, N. THE 13C NMR SPECTRA OF POLYETHER ANTIBIOTICS AND SOME EMPIRICAL RULES FOR STRUCTURAL STUDIES OF POLYETHER ANTIBIOTICS. 1982,17, 555. HETEROCYCLESa
  157679. GABRIEL WEATHERHEAD
  157680. 8474N
  157681. 2/28/96V
  157682. A REVIEW. NAGAO, Y.; FUJITA, E. A NEW PRACTICAL SYNTHETIC METHOD: MONITORED AMINOLYSIS OF 3 ACYL 1,3 THIAZOLIDINE 2 THIONE. HETEROCYCLESa
  157683. GABRIEL WEATHERHEAD
  157684. 8475N
  157685. 2/28/96V
  157686. A REVIEW. INUBUSHI, Y.; IBUKA, T. SYNTHESES OF L AZASPIRO [5.5]UNDECANES: STEREOSELECTIVE SYNTHESES OF PERHYDRO  AND OCTAHYDROHISTRIONICOTOXIN. 1982, 17, 507. HETEROCYCLESa
  157687. GABRIEL WEATHERHEAD
  157688. 8476N
  157689. 2/28/96VoA REVIEW.  KAMETANI, T.; FUKUMOTO, K.; IHARA, M. SYNTHESIS OF CARBAPENEM ANTIBIOTICS. 1982,17, 463 HETEROCYCLESa
  157690. GABRIEL WEATHERHEAD
  157691. 8477N
  157692. 2/28/96V
  157693. A REVIEW.  RIPPERGER, H.; SCHREIBER, K. NICOTIANAMINE AND ANALOGOUS AMINO ACIDS, ENDOGENOUS IRON CARRIERS IN HIGHER PLANTS. 1982,17, 447. HETEROCYCLES
  157694. GABRIEL WEATHERHEAD
  157695. 8478N
  157696. 2/28/96VmA REVIEW. WITKOP, B. PROBING ION CHANNELS WITH NATURAL AND SYNTHETIC HETEROCYCLES. 1982,17, 431. HETEROCYCLESa
  157697. GABRIEL WEATHERHEAD
  157698. 8479N
  157699. 2/28/96VhA REVIEW. AGRAWAL, P. K.; RASTOGI, R. P. 13C NMR SPECTROSCOPY OF FLAVONOIDS. 1981,16, 2181. HETEROCYCLESa
  157700. GABRIEL WEATHERHEAD
  157701. 8480N
  157702. 2/28/96V}A REVIEW.  BELSON, D. J.; STRACHAN, A. N. PREPARATION AND PROPERTIES OF ISOCYANIC ACID. 1982,11, 41. CHEMICAL SOCIETY REVIEWSa
  157703. GABRIEL WEATHERHEAD
  157704. 8481N
  157705. 2/28/96V
  157706. A REVIEW. HEELIS, P. F. THE PHOTOPHYSICAL AND PHOTOCHEMICAL PROPERTIES OF FLAVINS (ISOALLOXAZINES). 1982,11,15. CHEMICAL SOCIETY REVIEWSa
  157707. GABRIEL WEATHERHEAD
  157708. 8482N
  157709. 2/28/96V{A REVIEW.  STOUT, D. M.;MEYERS, A. I. RECENT ADVANCES IN THE CHEMISTRY OF DIHYDROPYRIDINES. 1982, 82, 223. CHEMICAL REVIEWSa
  157710. GABRIEL WEATHERHEAD
  157711. 8483N
  157712. 2/28/96
  157713. VtA REVIEW. TERRIER, F. RATE AND EQUILIBRIUM STUDIES IN JACKSON MEISENHEIMER COMPLEXES. 1982, 82, 77. CHEMICAL REVIEWSa
  157714. GABRIEL WEATHERHEAD
  157715. 8484N
  157716. 2/28/96V
  157717. A REVIEW.  MIRBACH, M. F.; MIRBACH, M. J.; SAUS, A. HIGH PRESSURE PHOTOCHEMISTRY AND ULTRAVIOLET SPECTROSCOPY IN GAS LIQUID SYSTEMS. 1982, 82, 59. CHEMICAL REVIEWSa
  157718. GABRIEL WEATHERHEAD
  157719. 8485N
  157720. 2/28/96V
  157721. A REVIEW. FREEDMAN, L. D.; DOAK, G. O. PREPARATION, REACTIONS AND PHYSICAL PROPERTIES OF ORGANOBISMUTH COMPOUNDS. 1982, 82, 15. CHEMICAL REVIEWSa
  157722. GABRIEL WEATHERHEAD
  157723. 8486N
  157724. 2/28/96VjA REVIEW. GAVEZZOTTI, A.; SIMONETTA, M. CRYSTAL CHEMISTRY IN ORGANIC SOLIDS. 1982, 82, 1. CHEMICAL REVIEWSa
  157725. GABRIEL WEATHERHEAD
  157726. 8487N
  157727. 2/28/96V
  157728. A REVIEW. KAUFFMANN, T. NEW POSSIBLE APPLICATIONS OF HEAVY MAIN GROUP ELEMENTS IN ORGANIC SYNTHESIS [NEW SYNTHETIC METHODS (36)]. 1982, 21, 410. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157729. GABRIEL WEATHERHEAD
  157730. 8488N
  157731. 2/28/96V
  157732. A REVIEW. FRANCK, B. TOPICAL PROBLEMS M THE BIOSYNTHESIS OF RED BLOOD PIGMENT. 1982, 21, 343. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157733. GABRIEL WEATHERHEAD
  157734. 8489N
  157735. 2/28/96
  157736. A REVIEW.  WENDT, H. THE REACTIVITY OF PRIMARY FREE RADICAL IONS, MASS TRANSFER, AND ELECTROSORPTION
  157737. THE FUNDAMENTAL FACTORS FOR SELECTIVITY IN ELECTROCHEMICAL SYNTHESES OF ORGNNIC COMPOUNDS. 1982, 21, 256. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  157738. GABRIEL WEATHERHEAD
  157739. 8490N
  157740. 2/28/96V
  157741. A REVIEW.  KABBE, H. J.; WIDDIG, A. SYNTHESIS AND REACTIONS OF 4 CHROMANONES. 1982, 21, 247. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157742. GABRIEL WEATHERHEAD
  157743. 8491N
  157744. 2/28/96V
  157745. A REVIEW. SCHAUMANN, E.; KETCHAM, R. [2 + 2] CYCLOREVERSIONS. 1982, 21, 225. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157746. GABRIEL WEATHERHEAD
  157747. 8492N
  157748. 2/28/96
  157749. A REVIEW. PAULSEN, H. ADVANCES IN SELECTIVE CHEMICAL SYNTHESES OF COMPLEX OLIGOSACCHARIDES. 1982, 21 155. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157750. GABRIEL WEATHERHEAD
  157751. 8493N
  157752. 2/28/96V
  157753. A REVIEW.  HERRMANN, W. A. ORGANOMETALLIC ASPECTS OF THE FISCHER TROPSCH SYNTHESIS. 1982, 21,117. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157754. GABRIEL WEATHERHEAD
  157755. 8494N
  157756. 2/28/96V
  157757. A REVIEW. REETZ, M. T. LEWIS ACID INDUCED A AIKYLATION OF CARBONYL COMPOUNDS [NEW SYNTHETIC METHODS (35)]. 1982, 21, 96. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157758. GABRIEL WEATHERHEAD
  157759. 8495N
  157760. 2/28/96V
  157761. A REVIEW. GROB C. A. THE NORBORNYL CATION: PROTOTYPE OF A 1,3 BRIDGED CARBOCATION. 1982, 21, 87. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157762. GABRIEL WEATHERHEAD
  157763. 8496N
  157764. 2/28/96
  157765. A REVIEW. HUNIG, S., SCHALLER, R. THE CHEMISTRY OF ACYL CYANIDES [NEW SYNTHETIC METHODS (34)]. 1982, 21, 36. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157766. GABRIEL WEATHERHEAD
  157767. 8497N
  157768. 2/28/96V
  157769. A REVIEW. CHANON, M.; TOBE, M. L. ELECTRON TRANSFER CATALYSIS: A MECHANISTIC CONCEPT FOR INORGANIC AND ORGANIC CHEMISTRY. 1982, 21, 1. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  157770. GABRIEL WEATHERHEAD
  157771. 8498N
  157772. 2/28/96VwA REVIEW. BLACK, T. H. RECENT APPLICATIONS OF HOMOGENEOUS CATALYSIS TO ORGANIC SYNTHESIS. 1982,15,13. ALDRICHIMICA ACTAa
  157773. GABRIEL WEATHERHEAD
  157774. 8499N
  157775. 2/28/96V
  157776. A REVIEW.  SCHUSTER, G. B., SCHMIDT, S. P. CHEMILUMINESCENCE OF ORGANIC COMPOUNDS. 1982,18,187. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  157777. GABRIEL WEATHERHEAD
  157778. 8500N
  157779. 2/28/96V|A REVIEW.  EBERSON, L. ELECTRON TRANSFER REACTIONS IN ORGANIC CHEMISTRY. 1982,18, 79. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  157780. GABRIEL WEATHERHEAD
  157781. 8501N
  157782. 2/28/96V
  157783. A REVIEW. TOULLEC, J. ENOLISATION OF SIMPLE CARBONYL COMPOUNDS AND RELATED REACTIONS. 1982,18,1. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  157784. GABRIEL WEATHERHEAD
  157785. 8502N
  157786. 2/28/96V
  157787. A REVIEW.  THAYER, J. S., BRINHNAN, F. E. THE BIOLOGICAL METHYLATION OF METALS AND METALLOIDS. 1982, 20, 314. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157788. GABRIEL WEATHERHEAD
  157789. 8503N
  157790. 2/28/96V
  157791. A REVIEW. CORRIU, R. J. P., GUERIN, C. NUCLEOPHILIC DISPLACEMENT AT SILICON: RECENT DEVELOPMENTS AND MECHANISTIC IMPLICATIONS. 1982, 20, 265. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157792. GABRIEL WEATHERHEAD
  157793. 8504N
  157794. 2/28/96VbA REVIEW. HERRMANN, W. A. THE METHYLENE BRIDGE. 1982, 20,160. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157795. GABRIEL WEATHERHEAD
  157796. 8505N
  157797. 2/28/96VcA REVIEW. HUANG, Y. Z.; SHEN, Y. C. ARSONIUM YLIDES. 1982, 20, ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157798. GABRIEL WEATHERHEAD
  157799. 2/28/96VcA REVIEW. ANDERSON, G. K. THE ORGANIC CHEMISTRY OF GOLD. 1982, ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157800. GABRIEL WEATHERHEAD
  157801. 8507N
  157802. 2/28/96VmA REVIEW. GLADYSZ, J. A. TRANSITION METAL FORMYL COMPLEXES. 1982, 20, 1. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  157803. GABRIEL WEATHERHEAD
  157804. 8508N
  157805. 2/28/96V
  157806. A REVIEW. DAVIDSON, J. L., PRESTON, P. N. USE OF TRANSITION ORGANOMETALLIC COMPOUNDS IN HETEROCYCLIC SYNTHESIS. 1982, 30, 321. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157807. GABRIEL WEATHERHEAD
  157808. 8509N
  157809. 2/28/96V|A REVIEW.  REID, S. T. PHOTOCHEMISTRY OF NITROGEN CONTAINING HETEROCYCLES. 1982, 30, 239. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157810. GABRIEL WEATHERHEAD
  157811. 8510N
  157812. 2/28/96VrA REVIEW. DEAN, F. M. RECENT ADVANCES IN FURAN CHEMISTRY. PART I. 1982, 30,168. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157813. GABRIEL WEATHERHEAD
  157814. 8511N
  157815. 2/28/96
  157816. VYA REVIEW. HORNFELDT, A. B. SELENOPHENES. 1982, 30,127. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157817. GABRIEL WEATHERHEAD
  157818. 8512N
  157819. 2/28/96VWA REVIEW. SASAKI, T. HETEROADAMANTANE. 1982, 30, 80. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157820. GABRIEL WEATHERHEAD
  157821. 8513N
  157822. 2/28/96VyA REVIEW.  DAVIS, M. SULFUR TRANSFER REAGENTS IN HETEROCYCLIC SYNTHESIS. 1982, 30, 48. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157823. GABRIEL WEATHERHEAD
  157824. 8514N
  157825. 2/28/96VyA REVIEW.  MOODY, C. J. AZODICARBONYL COMPOUNDS IN HETEROCYCLIC SYNTHESIS. 1982, 30,1. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  157826. GABRIEL WEATHERHEAD
  157827. 8515N
  157828. 2/28/96V
  157829. A REVIEW.  CERVENY, L.; RUZICKA, V. SOLVENT AND STRUCTURE EFFECTS IN HYDROGENATION OF UNSATURATED SUBSTANCES ON SOLID CATALYSTS. 1981, 30. ADVANCES IN CATALYSISa
  157830. GABRIEL WEATHERHEAD
  157831. 8516N
  157832. 2/28/96
  157833. A REVIEW. BILOEN, P.; SACHTLER, W. M. H. MECHANISM OF HYDROCARBON SYNTHESIS OVER FISCHER TROPSCH CATALYSTS. 1981, 30. ADVANCES IN CATALYSISa
  157834. GABRIEL WEATHERHEAD
  157835. 8517N
  157836. 2/28/96V
  157837. A REVIEW. GRASSELLI, R. K.; BURRINGTON, J. D. SELECTIVE OXIDATION AND AMMOXIDATION OF PROPYLENE BY HETEROGENEOUS CATALYSIS. 1981, 30. ADVANCES IN CATALYSISa
  157838. GABRIEL WEATHERHEAD
  157839. 8518N
  157840. 2/28/96VvA REVIEW. GAULT, F. G. MECHANISMS OF SKELETAL ISOMERIZATION OF HYDROCARBONS ON METALS. 1981, 30. ADVANCES IN CATALYSISa
  157841. GABRIEL WEATHERHEAD
  157842. 8519N
  157843. 2/28/96VsA REVIEW. SUZUKI A. ORGANOBORATES IN NEW SYNTHETIC REACTIONS. 1982, 15 178. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157844. GABRIEL WEATHERHEAD
  157845. 8520N
  157846. 2/28/96V
  157847. A REVIEW.  ROSSI, R. A. PHENOMENON OF RADICAL ANION FRAGMENTATION IN THE COURSE OF AROMATIC SHN1 REACTIONS. 1982,15,164. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157848. GABRIEL WEATHERHEAD
  157849. 8521N
  157850. 2/28/96
  157851. A REVIEW. OPPOLZER, W. INTRAMOLECULAR [2 + 2] PHOTOADDITION/ CYCLOBUTANE FRAGMENTATION SEQUENCE M ORGANIC SYNTHESIS. 1982, 15, 135. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157852. GABRIEL WEATHERHEAD
  157853. 8522N
  157854. 2/28/96V
  157855. A REVIEW.  LEONARD, N. J. DIMENSIONAL PROBES OF ENZYME COENZYME BINDING SITES. 1982,15,128. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157856. GABRIEL WEATHERHEAD
  157857. 8523N
  157858. 2/28/96V
  157859. A REVIEW. BENTRUDE, W. G. PHOSPHORANYL RADICALS: THEIR STRUCTURE, FORMATION, AND REACTIONS. 1982,15,117. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157860. GABRIEL WEATHERHEAD
  157861. 8524N
  157862. 2/28/96V{A REVIEW. HUANG, N. Z.; SONDHEIMER, F. THE PLANAR DEHYDRO[8]ANNULENES. 1982,15, 96. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157863. GABRIEL WEATHERHEAD
  157864. 8525N
  157865. 2/28/96V
  157866. A REVIEW. MATTES, S. L., FARID, S. PHOTOCHEMICAL CYCLOADDITIONS VIA EXCIPLEXES, EXCITED COMPLEXES, AND RADICAL IONS. 1982, 15, 80. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  157867. GABRIEL WEATHERHEAD
  157868. 8526N
  157869. 2/28/96V
  157870. A REVIEW.  TABUSHI, I. CYCLODEXTRIN CATALYSIS AS A MODEL FOR ENZYME ACTION. 1982,15, 66. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157871. GABRIEL WEATHERHEAD
  157872. 8527N
  157873. 2/28/96V_A REVIEW.  DIMROTH, K. THE L5 PHOSPHORINS. 1982,15, 58. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157874. GABRIEL WEATHERHEAD
  157875. 8528N
  157876. 2/28/96VxA REVIEW. SCOTT, L. T. THERMAL REARRANGEMENT OF AROMATIC COMPOUNDS. 1982,15, 52. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157877. GABRIEL WEATHERHEAD
  157878. 8529N
  157879. 2/28/96V
  157880. A REVIEW. FARCASIU, D. PROTONATION OF SIMPLE AROMATICS IN SUPERACIDS. A REEXAMINATION. 1982,15, 46. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157881. GABRIEL WEATHERHEAD
  157882. 8530N
  157883. 2/28/96V
  157884. A REVIEW. MAIER, J. P. OPEN SHELL ORGANIC CATIONS: SPECTROSCOPIC STUDIES BY MEANS OF THEIR RADIATIVE DECAY IN THE GAS PHASE. 1982,15, 18. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157885. GABRIEL WEATHERHEAD
  157886. 8531N
  157887. 2/28/96VpA REVIEW. BOCK, H.; KAIM, W. ORGANOSILICON RADICAL CATIONS. 1982, 15, 9. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  157888. GABRIEL WEATHERHEAD
  157889. 8532N
  157890. 2/28/96V
  157891. A REVIEW. DEV, S.; YADAV, J. S., NARULA, A. CRC HANDBOOK OF TERPENOIDS. MONOTERPENOIDS. VOLUMES I AND II, CRC PRESS: BOCA RATON, FL, 1982.a
  157892. GABRIEL WEATHERHEAD
  157893. 8533N
  157894. 2/28/96VQA REVIEW. SANDSTROM, J. DYNAMIC NMR SPECTROSCOPY, ACADEMIC PRESS: NEW YORK, 1982.a
  157895. GABRIEL WEATHERHEAD
  157896. 8534N
  157897. 2/28/96V`A REVIEW.  SALEM, L. ELECTRONS IN CHEMICAL REACTIONS: FIRST PRINCIPLES, WILEY: NEW JERSEY, 1982.a
  157898. GABRIEL WEATHERHEAD
  157899. 8535N
  157900. 2/28/96V
  157901. A REVIEW. NEWKOME, G. R., PAUDLER, W. W. CONTEMPORARY HETEROCYCLIC CHEMISTRY: SYNTHESES, REACTIONS, AND APPLICATIONS, WILEY: NEW JERSEY, 1982.a
  157902. GABRIEL WEATHERHEAD
  157903. 8536N
  157904. 2/28/96
  157905. V[A REVIEW.  MEMORY, J. D.; WILSON, N. K. NMR OF AROMATIC COMPOUNDS, WILEY: NEW JERSEY, 1982.a
  157906. GABRIEL WEATHERHEAD
  157907. 8537N
  157908. 2/28/96VpA REVIEW.  MANN, B. E.; TAYLOR, B. F. 13C NMR DATA FOR ORGANOMETALLIC COMPOUNDS, ACADEMIC PRESS: NEW YORK, 1981.a
  157909. GABRIEL WEATHERHEAD
  157910. 8538N
  157911. 2/28/96VsA REVIEW. KRSTULOVIC, A. M.; BROWN, P. R. REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY, WILEY: NEW JERSEY,a
  157912. GABRIEL WEATHERHEAD
  157913. 8539N
  157914. 2/28/96VmA REVIEW. GOKEL, G. W.; KORZENIOWSKI, S. H. MACROCYCLIC POLYETHER SYNTHESES, SPRINGER VERLAG: NEW YORK, 1982.a
  157915. GABRIEL WEATHERHEAD
  157916. 8540N
  157917. 2/28/96ViA REVIEW.  DE LA MARE, P. B. D. ELECTROPHILIC ADDITIONS TO UNSATURATED SYSTEMS, ELSEVIER: NEW YORK, 1982.a
  157918. GABRIEL WEATHERHEAD
  157919. 8541N
  157920. 2/28/96VBA REVIEW.  BORDEN, W. T., ED. DIRADICALS, WILEY: NEW JERSEY, 1982.a
  157921. GABRIEL WEATHERHEAD
  157922. 8542N
  157923. 2/28/96
  157924. A REVIEW. BALABAN, A. T.; FISCHER, G. W.; DINCULESCU, A.; DOROFEENKO, G. N.; KOBLIK, A. V.; MEZHERITSKII, V. V., SCHROTH W. PYRYLIUM SALTS. SYNTHESES, REACTIONS, AND PHYSICAL PROPERTIES. ACADEMIC PRESS: NEW YORK, 1982.a
  157925. GABRIEL WEATHERHEAD
  157926. 8543N
  157927. 2/28/96V
  157928. A REVIEW. SETO, H.; OTAKE, N. 13C NMR SPECTRA OF POLYETHER ANTIBIOTICS. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.a
  157929. GABRIEL WEATHERHEAD
  157930. 8544N
  157931. 2/28/96
  157932. A REVIEW.  ANTEUNIS, M. J. O. STRUCTURE, CONFORMATION AND MECHANISM OF ACTION OF POLYETHER ANTIBIOTICS AS REVEALED BY PROTON NMR. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.
  157933. GABRIEL WEATHERHEAD
  157934. 8545N
  157935. 2/28/96
  157936. A REVIEW. OCCOLOWITZ, J. L.; HAMILL, R. L. MASS SPECTROMETRY OF POLYETHER ANTIBIOTICS. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.a
  157937. GABRIEL WEATHERHEAD
  157938. 8546N
  157939. 2/28/96V
  157940. A REVIEW. DUESLER, E. N., PAUL, I. C. THE X RAY STRUCTURES OF THE POLYETHER ANTIBIOTICS. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.a
  157941. GABRIEL WEATHERHEAD
  157942. 8547N
  157943. 2/28/96V
  157944. A REVIEW. WESTLEY, J. W. CHEMICAL TRANSFORMATIONS OF POLYETHER ANTIBIOTICS. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.a
  157945. GABRIEL WEATHERHEAD
  157946. 8548N
  157947. 2/28/96
  157948. A REVIEW. KISHI, Y. CHEMICAL SYNTHESIS. POLYETHER ANTIBIOTICS. NATURALLY OCCURRING ACID IONOPHORES, VOLUME 2: CHEMISTRY, J. W. WESTLEY, ED., MARCEL DEKKER: NEW YORK, 1983.a
  157949. GABRIEL WEATHERHEAD
  157950. 8549N
  157951. 2/28/96V
  157952. A REVIEW. HAYATSU, R.; SCOTT, R. G.; WINANS, R. E. OXIDATION OF COAL. ORGANIC CHEMISTRY. OXIDATION IN ORGANIC CHEMISTRY, PART D, W. S. TRAHANOVSKY, ED. ACADEMIC PRESS: NEW YORK, 1982.a
  157953. GABRIEL WEATHERHEAD
  157954. 8550N
  157955. 2/28/96V
  157956. A REVIEW. DHINGRA, O. P. INTRAMOLECULAR OXIDATIVE COUPLING OF AROMATIC SUBSTRATES. ORGANIC CHEMISTRY. OXIDATION IN ORGANIC CHEMISTRY, PART D, W. S. TRAHANOVSKY, ED. ACADEMIC PRESS: NEW YORK, 1982.a
  157957. GABRIEL WEATHERHEAD
  157958. 8551N
  157959. 2/28/96V
  157960. A REVIEW. LEE, D. G. PHASE TRANSFER ASSISTED PERMANGANATE OXIDATIONS. ORGANIC CHEMISTRY. OXIDATION IN ORGANIC CHEMISTRY, PART D, W. S. TRAHANOVSKY, ED. ACADEMIC PRESS: NEW YORK, 1982.a
  157961. GABRIEL WEATHERHEAD
  157962. 8552N
  157963. 2/28/96
  157964. A REVIEW.  RUBOTTOM, G. M. OXIDATIONS WITH LEAD TETRAACETATE. ORGANIC CHEMISTRY. OXIDATION IN ORGANIC CHEMISTRY, PART D, W. S. TRAHANOVSKY, ED. ACADEMIC PRESS: NEW YORK, 1982.a
  157965. GABRIEL WEATHERHEAD
  157966. 8553N
  157967. 2/28/96V
  157968. A REVIEW. TAYLOR, R. J. K. SYNTHESIS OF PGI2 (PROSTACYCLIN) ANALOGUES. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157969. GABRIEL WEATHERHEAD
  157970. 8554N
  157971. 2/28/96V
  157972. A REVIEW. TAYLOR, R. J. K. SYNTHESIS OF THROMBOXANE ANALOGUES. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157973. GABRIEL WEATHERHEAD
  157974. 8555N
  157975. 2/28/96V
  157976. A REVIEW. TAYLOR, R. J. K. SYNTHESIS OF ANALOGUES OF PROSTAGLANDIN ENDOPEROXIDES. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157977. GABRIEL WEATHERHEAD
  157978. 8556N
  157979. 2/28/96
  157980. A REVIEW.  TAYLOR, R. J. K. SYNTHESIS OF NATURALLY OCCURRING PROSTAGLANDIN ENDOPEROXIDES, THROMBOXANES AND PROSTAGLANDIN I2 (PROSTACYCLIN). NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.
  157981. GABRIEL WEATHERHEAD
  157982. 8557N
  157983. 2/28/96V
  157984. A REVIEW. CATON, M. P. L. RECENT SYNTHESES OF PROSTAGLANDINS VIA CONJUGATE ADDITION TO CYCLOPENTENONES. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157985. GABRIEL WEATHERHEAD
  157986. 8558N
  157987. 2/28/96V
  157988. A REVIEW.  NEWTON, R. F. RECENT SYNTHESES OF PROSTAGLANDINS VIA POLYCYCLIC INTERMEDIATES. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157989. GABRIEL WEATHERHEAD
  157990. 8559N
  157991. 2/28/96
  157992. A REVIEW. ROBERTS, S. M. SYNTHETIC ROUTES TO PROSTAGLANDINS PUBLISHED BEFORE 1977. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157993. GABRIEL WEATHERHEAD
  157994. 8560N
  157995. 2/28/96V
  157996. A REVIEW. SCHEINMANN, F. INTRODUCTION, NOMENCLATURE AND BIOSYNTHESIS OF EICOSANOIDS. NEW SYNTHETIC ROUTES TO PROSTAGLANDINS AND THROMBOXANES, S. M. ROBERTS AND F. SCHEINMANN EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  157997. GABRIEL WEATHERHEAD
  157998. 8561N
  157999. 2/28/96V
  158000. A REVIEW. THEIMER, E. T. BENZENE DERIVED CYCLIC CARBINOLS. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158001. GABRIEL WEATHERHEAD
  158002. 8562N
  158003. 2/28/96V
  158004. A REVIEW.  HEROUT, V. SESQUITERPENE ALCOHOLS. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158005. GABRIEL WEATHERHEAD
  158006. 8563N
  158007. 2/28/96
  158008. A REVIEW. TRASS, P. C. ADVANCES IN THE CHEMISTRY OF SOME INTERESTING CYCLIC MONOTERPENE ALCOHOLS. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158009. GABRIEL WEATHERHEAD
  158010. 8564N
  158011. 2/28/96V
  158012. A REVIEW.  BOELENS, H. ACYCLIC MONOTERPENE ALCOHOLS WITH 2,6 DIMETHYLOCTANE SKELETON. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158013. GABRIEL WEATHERHEAD
  158014. 8565N
  158015. 2/28/96V
  158016. A REVIEW.  BEETS, M. G. J. ODOR AND STIMULANT STRUCTURE. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158017. GABRIEL WEATHERHEAD
  158018. 8566N
  158019. 2/28/96V
  158020. A REVIEW. AMOORE, J. E. ODOR THEORY AND ODOR CLASSIFICATION. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158021. GABRIEL WEATHERHEAD
  158022. 8567N
  158023. 2/28/96
  158024. A REVIEW. GETCHELL, T. V.; GETCHELL, M. L. PHYSIOLOGY OF VERTEBRATE OLFACTORY CHEMORECEPTION. FRAGRANCE CHEMISTRY. THE SCIENCE OF THE SENSE OF SMELL, E. T. THEIMER, ED., ACADEMIC PRESS: NEW YORK, 1982.a
  158025. GABRIEL WEATHERHEAD
  158026. 8568N
  158027. 2/28/96V
  158028. A REVIEW. JONES, G.; BATY, D. J. QUINOLINE N OXIDES, P 377. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. QUINOLINES, PART II, G. JONES, ED., WILEY INTERSCIENCE: NEW YORK, 1982.a
  158029. GABRIEL WEATHERHEAD
  158030. 8569N
  158031. 2/28/96V
  158032. A REVIEW. POPP, F. D. REISSERT COMPOUNDS AND RELATED N ACYLDIHYDROQUINOLINES, P 353. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. QUINOLINES, PART II, G. JONES, ED., WILEY INTERSCIENCE: NEW YORK, 1982.a
  158033. GABRIEL WEATHERHEAD
  158034. 8570N
  158035. 2/28/96V
  158036. A REVIEW.  CLARET, P. A.; OSBORNE, A. G. ALKYLQUINOLINES AND ARYLQUINOLINES, P 1. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. QUINOLINES, PART II, G. JONES, ED., WILEY INTERSCIENCE: NEW YORK, 1982.a
  158037. GABRIEL WEATHERHEAD
  158038. 8571N
  158039. 2/28/96
  158040. A REVIEW. LANDOR, P. D. EXPERIMENTAL TECHNIQUES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158041. GABRIEL WEATHERHEAD
  158042. 8572N
  158043. 2/28/96V
  158044. A REVIEW.  RUNGE, W. SPECTRA OF ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158045. GABRIEL WEATHERHEAD
  158046. 8573N
  158047. 2/28/96V
  158048. A REVIEW.  CLAESSON, A.; OLSSON, L. I. ALLENIC INTERMEDIATES IN ORGANIC SYNTHESIS. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158049. GABRIEL WEATHERHEAD
  158050. 8574N
  158051. 2/28/96V
  158052. A REVIEW. CLAESSON, A. BIOLOGICALLY ACTIVE ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158053. GABRIEL WEATHERHEAD
  158054. 8575N
  158055. 2/28/96V
  158056. A REVIEW. LANDOR, S. R. NATURALLY OCCURRING ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158057. GABRIEL WEATHERHEAD
  158058. 8576N
  158059. 2/28/96V
  158060. A REVIEW. RUNGE, W. STEREOCHEMISTRY OF ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 3. STEREOCHEMICAL, SPECTROSCOPIC AND SPECIAL ASPECTSa
  158061. GABRIEL WEATHERHEAD
  158062. 8577N
  158063. 2/28/96V
  158064. A REVIEW. LANDOR, S. R.; HOPF, H.; JACOBS, T. L. REACTIONS OF ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 2. REACTIONSa
  158065. GABRIEL WEATHERHEAD
  158066. 8578N
  158067. 2/28/96V
  158068. A REVIEW. LANDOR, P. D. SYNTHESIS OF ALLENES AND CONJUGATED ALLENES. THE CHEMISTRY OF ALLENES, S. R. LANDOR, ED., ACADEMIC PRESS: NEW YORK, 1983. VOLUME 1. SYNTHESISa
  158069. GABRIEL WEATHERHEAD
  158070. 8579N
  158071. 2/28/96
  158072. A REVIEW.  KOSTER, W. H.; CIMARUSTI, C. M.; SYKES, R. B. MONOBACTAMS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158073. GABRIEL WEATHERHEAD
  158074. 8580N
  158075. 2/28/96
  158076.  A REVIEW. SHOCKMAN, G. D.; DANEO MOORE, L.; MCDOWELL, T. D.; WONG, W. THE RELATIONSHIP BETWEEN INHIBITION OF CELL WALL SYNTHESIS AND BACTERIAL LETHALITY. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRY
  158077. GABRIEL WEATHERHEAD
  158078. 8581N
  158079. 2/28/96V
  158080. A REVIEW. KAMMER, R. B. B LACTAM ANTIBIOTICS IN CLINICAL MEDICINE. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158081. GABRIEL WEATHERHEAD
  158082. 8582N
  158083. 2/28/96
  158084. A REVIEW. WAXMAN D. J. STROMINGER, J. L. B LACTAM ANTIBIOTICS: BIOCHEMICAL MODES OF ACTION. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158085. GABRIEL WEATHERHEAD
  158086. 8583N
  158087. 2/28/96V
  158088. A REVIEW.  SYKES, R. B.; BUSH, K. PHYSIOLOGY, BIOCHEMISTRY, AND INACTIVATION OF B LACTAMASES. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158089. GABRIEL WEATHERHEAD
  158090. 8584N
  158091. 2/28/96V
  158092. A REVIEW. ELANDER, R. P.; AOKI, H. ,B LACTAM PRODUCING MICROORGANISMS: THEIR BIOLOGY AND FERMENTATION BEHAVIOR. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158093. GABRIEL WEATHERHEAD
  158094. 8585N
  158095. 2/28/96
  158096. A REVIEW. QUEENER, S. W.; NEUSS, N. THE BIOSYNTHESIS OF B LACTAM ANTIBIOTICS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 3. BIOCHEMISTRYa
  158097. GABRIEL WEATHERHEAD
  158098. 8586N
  158099. 2/28/96V
  158100. A REVIEW.  CHERRY, P. C.; NEWALL, C. E. CLAVULANIC ACID. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 2. NONTRADITIONAL B LACTAM ANTIBIOTICSa
  158101. GABRIEL WEATHERHEAD
  158102. 8587N
  158103. 2/28/96V
  158104. A REVIEW. RATCLIFFE, R. W.; ALBERS SCHONBERG, G. THE PENEMS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 2. NONTRADITIONAL B LACTAM ANTIBIOTICSa
  158105. GABRIEL WEATHERHEAD
  158106. 8588N
  158107. 2/28/96
  158108. A REVIEW.  KAMIYA, T.; AOKI, H.; MINE, Y. NOCARDICINS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 2. NONTRADITIONAL B LACTAM ANTIBIOTICSa
  158109. GABRIEL WEATHERHEAD
  158110. 8589N
  158111. 2/28/96
  158112. A REVIEW.  HOLDEN, K. G. TOTAL SYNTHESIS OF PENICILLINS, CEPHALOSPORINS AND THEIR NUCLEAR ANALOGS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 2. NONTRADITIONAL B LACTAM ANTIBIOTICS
  158113. GABRIEL WEATHERHEAD
  158114. 8590N
  158115. 2/28/96
  158116. A REVIEW. NAGATA, W., NARISADA, M., YOSHIDA, T. PARTIAL SYNTHESIS OF NUCLEAR ANALOGS OF CEPHALOSPORINS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 2. NONTRADITIONAL B LACTAM ANTIBIOTICS
  158117. GABRIEL WEATHERHEAD
  158118. 8591N
  158119. 2/28/96
  158120. A REVIEW. BOYD, D. B. THEORETICAL AND PHYSICOCHEMICAL STUDIES ON B LACTAM ANTIBIOTICS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 1. PENICILLINS AND CEPHALOSPORINSa
  158121. GABRIEL WEATHERHEAD
  158122. 8592N
  158123. 2/28/96
  158124. A REVIEW. WEBBER, J. A.; WHELLER, W. J. ANTIMICROBIAL AND PHARMACOKINETIC PROPERTIES OF NEWER PENICILLINS AND CEPHALOSPORINS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 1. PENICILLINS AND CEPHALOSPORINS
  158125. GABRIEL WEATHERHEAD
  158126. 8593N
  158127. 2/28/96V
  158128. A REVIEW. GORDON, E. M.; SYKES, R. B. CEPHAMYCIN ANTIBIOTICS. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 1. PENICILLINS AND CEPHALOSPORINSa
  158129. GABRIEL WEATHERHEAD
  158130. 8594N
  158131. 2/28/96
  158132. A REVIEW. KUKOLJA, S.; CHAUVETTE, R. R. CEPHALOSPORIN ANTIBIOTICS PREPARED AT THE C 3 POSITION. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 1. PENICILLINS AND CEPHALOSPORINSa
  158133. GABRIEL WEATHERHEAD
  158134. 8595N
  158135. 2/28/96V
  158136. A REVIEW. COOPER, R. D. G.; KOPPEL, G. A. THE CHEMISTRY OF PENICILLIN SULFOXIDE. CHEMISTRY AND BIOLOGY OF B LACTAM ANTIBIOTICS, R. B. MORIN AND M. GORMAN, EDS., ACADEMIC PRESS: NEW YORK, 1982. VOLUME 1. PENICILLINS AND CEPHALOSPORINSa
  158137. GABRIEL WEATHERHEAD
  158138. 8596N
  158139. 2/28/96V
  158140. A REVIEW. DURAN, N. SINGLET OXYGEN IN BIOLOGICAL PROCESSES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158141. GABRIEL WEATHERHEAD
  158142. 8597N
  158143. 2/28/96
  158144. A REVIEW. ALLEN, R. C. BIOCHEMIEXCITATION: CHEMILUMINESCENCE AND THE STUDY OF BIOLOGICAL OXYGENATION REACTIONS. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158145. GABRIEL WEATHERHEAD
  158146. 8598N
  158147. 2/28/96V
  158148. A REVIEW. CILENTE, G. ELECTRONIC EXCITATION IN DARK BIOLOGICAL PROCESSES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158149. GABRIEL WEATHERHEAD
  158150. 8599N
  158151. 2/28/96V
  158152. A REVIEW. SHIMOMURA, O. MECHANISM OF BIOLUMINESCENCE. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158153. GABRIEL WEATHERHEAD
  158154. 8600N
  158155. 2/28/96V
  158156. A REVIEW. SCHUSTER, G. B.; HORN, K. A. CHEMICALLY INITIATED ELECTRON EXCHANGE LUMINESCENCE. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158157. GABRIEL WEATHERHEAD
  158158. 8601N
  158159. 2/28/96V
  158160. A REVIEW.  FAULKNER, L. R.; GLASS, R. S. ELECTROCHEMIIUMINESCENCES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158161. GABRIEL WEATHERHEAD
  158162. 8602N
  158163. 2/28/96V
  158164. A REVIEW.  ADAM, W.; ZINNER, K. DETERMINATION OF ACTIVATION PARAMETERS AND THE THERMAL STABILITY OF 1 2 DIOXETANES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158165. GABRIEL WEATHERHEAD
  158166. 8603N
  158167. 2/28/96V
  158168. A REVIEW. ADAM, W. DETERMINATION OF CHEMI EXCITATION YIELDS IN THE THERMAL GENERATION OF ELECTRONIC EXCITATION FROM 1,2 DIOXETANES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158169. GABRIEL WEATHERHEAD
  158170. 8604N
  158171. 2/28/96
  158172. A REVIEW. KOPECKY, K. R. SYNTHESIS OF 1,2 DIOXETANES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158173. GABRIEL WEATHERHEAD
  158174. 8605N
  158175. 2/28/96V
  158176. A REVIEW. BOGAN, D. J. GAS PHASE DIOXETANE CHEMILUMINESCENCES. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158177. GABRIEL WEATHERHEAD
  158178. 8606N
  158179. 2/28/96V
  158180. A REVIEW. QUNIA, F. H. PHOTOPHYSICAL CONCEPTS IN CONDENSED MEDIA. CHEMICAL AND BIOLOGICAL GENERATION OF EXCITED STATES, W. ADAM AND G. CILENTO, EDS., ACADEMIC PRESS: NEW YORK, 1982.a
  158181. GABRIEL WEATHERHEAD
  158182. 8607N
  158183. 2/28/96VcA REVIEW. MARGARETHA, P. PREPARATIVE ORGANIC PHOTOCHEMISTRY. 1982, 103. TOPICS IN CURRENT CHEMISTRYa
  158184. GABRIEL WEATHERHEAD
  158185. 8608N
  158186. 2/28/96
  158187. $V~A REVIEW.  MONTANARI, F.; LANDINI, D.; ROLLA, F. PHASE TRANSFER CATALYZED REACTIONS. 1982,102,147. TOPICS IN CURRENT CHEMISTRYa
  158188. GABRIEL WEATHERHEAD
  158189. 8609N
  158190. 2/28/96V
  158191. A REVIEW. KELLOGG, R. M. BIOORGANIC MODELLING
  158192. STEREOSELECTIVE REACTIONS WITH CHIRAL NEUTRAL LIGAND COMPLEXES AS MODEL SYSTEMS FOR ENZYME CATALYSIS. 1982,102,111. TOPICS IN CURRENT CHEMISTRYa
  158193. GABRIEL WEATHERHEAD
  158194. 8610N
  158195. 2/28/96V
  158196. A REVIEW. PAINTER, G. R.; PRESSMAN, B. C. DYNAMIC ASPECTS OF IONOPHORE MEDIATED MEMBRANE TRANSPORT. 1982,102, 83. TOPICS IN CURRENT CHEMISTRYa
  158197. GABRIEL WEATHERHEAD
  158198. 8611N
  158199. 2/28/96V
  158200. A REVIEW. HILGENFELD, R.; SAENGER, W. STRUCTURAL CHEMISTRY OF NATURAL AND SYNTHETIC IONOPHORES AND THEIR COMPLEXES WITH CATIONS. 1982,102, 1. TOPICS IN CURRENT CHEMISTRYa
  158201. GABRIEL WEATHERHEAD
  158202. 8612N
  158203. 2/28/96ViA REVIEW.  NEWTON, C. G., RAMSDEN, C. A. MESO IONIC HETEROCYCLES (1976 1980). 1982, 38, 2965. TETRAHEDRON
  158204. GABRIEL WEATHERHEAD
  158205. 8613N
  158206. 2/28/96VfA REVIEW.  VEDEJS, E.; KRAFFT, G. A. CYCLIC SULFIDES IN ORGANIC SYNTHESIS. 1982, 38, 2857. TETRAHEDRONa
  158207. GABRIEL WEATHERHEAD
  158208. 8614N
  158209. 2/28/96VkA REVIEW.  TAYLOR, K. G. CARBENEGS AND CARBENOIDS WITH NEIGHBORING HETEROATOMS. 1982, 38, 2751. TETRAHEDRONa
  158210. GABRIEL WEATHERHEAD
  158211. 8615N
  158212. 2/28/96VjA REVIEW.  WILSON, G. E., JR. STRUCTURE AND REACTIVITY OF HALOSULFONIUM SALTS. 1982, 38, 2597. TETRAHEDRONa
  158213. GABRIEL WEATHERHEAD
  158214. 8616N
  158215. 2/28/96V
  158216. A REVIEW.  WHITTEN, D. G.; RUSSELL, J. C.; SCHMEHL, R. H. PHOTOCHEMICAL REACTIONS IN ORGANIZED ASSEMBLIES: ENVIRONMENTAL EFFECTS ON REACTIONS OCCURRING IN MICELLES, VESICLES, FILMS AND MULTILAYER ASSEMBLIES AND AT INTERFACES. 1982, 38, 2455. TETRAHEDRONa
  158217. GABRIEL WEATHERHEAD
  158218. 8617N
  158219. 2/28/96VsA REVIEW.  OLAH, G. A.; NARANG S. C. IODOTRIMETHYLSILANE
  158220. A VERSATILE SYNTHETIC REAGENT. 1982, 38, 2225. TETRAHEDRON
  158221. GABRIEL WEATHERHEAD
  158222. 8618N
  158223. 2/28/96V
  158224. A REVIEW. HICKMOTT, P. W. ENAMINES: RECENT ADVANCES IN SYNTHETIC, SPECTROSCOPIC, MECHANISTIC, AND STEREOCHEMICAL ASPECTS
  158225. 1. 1982, 38 1975. TETRAHEDRONa
  158226. GABRIEL WEATHERHEAD
  158227. 8619N
  158228. 2/28/96VgA REVIEW. KRAPCHO A. P. SYNTHETIC APPLICATIONS OF DEALKOXYCARBONYLATIONS. PART II. 1982, 893. SYNTHESISa
  158229. GABRIEL WEATHERHEAD
  158230. 8620N
  158231. 2/28/96V
  158232. A REVIEW. KRAPCHO, A. P. SYNTHETIC APPLICATIONS OF DEALKOXYCARBONYLATIONS OF MALONATE ESTERS, B KETO ESTERS, A CYANO ESTERS AND RELATED COMPOUNDS IN DIPOLAR APROTIC MEDIA
  158233. PART 1. 1982, 805. SYNTHESISa
  158234. GABRIEL WEATHERHEAD
  158235. 8621N
  158236. 2/28/96V
  158237. A REVIEW.  DEEM, M. L. EXPANDED RING SYSTEMS FROM CYCLOPROPENES: 1,3 DIPOLAR AND [2 + 2] ADDITIONS ACROSS THE CYCLOPROPENYL P BOND. 1982, 701. SYNTHESISa
  158238. GABRIEL WEATHERHEAD
  158239. 8622N
  158240. 2/28/96
  158241. A REVIEW.  TRAMONTINI, M. STEREOSELECTIVE SYNTHESIS OF DIASTEREOMERIC AMINO ALCOHOLS FROM CHIRAL AMINOCARBONYL COMPOUNDS BY REDUCTION OR BY ADDITION OF ORGANOMETALLIC REAGENTS. 1982, 605. SYNTHESISa
  158242. GABRIEL WEATHERHEAD
  158243. 8623N
  158244. 2/28/96V~A REVIEW. PETRAGNANI, N., YONASHIRO, M. THE REACTIONS OF DIANIONS OF CARBOXYLIC ACIDS AND ESTER ENOLATES. 1982, 521. SYNTHESISa
  158245. GABRIEL WEATHERHEAD
  158246. 8624N
  158247. 2/28/96V
  158248. A REVIEW. AGABABYAN, A. G., GEVORGYAN, G. A.; MNDZHOYAN, 0. L. AMINO ACIDS AS THE AMINE COMPONENT IN THE MANNICH REACTION. 1982, 51, 387. RUSSIAN CHEMICAL REVIEWSa
  158249. GABRIEL WEATHERHEAD
  158250. 8625N
  158251. 2/28/96V
  158252. A REVIEW. AFANAS'EV, V. A.; DZHAMANBAEV, ZH. A. ZAIKOV, G. E. DERIVATIVES OF CARBOHYDRATES WITH CARBAMIDE FRAGMENTS. 1982, 51, 377. RUSSIAN CHEMICAL REVIEWSa
  158253. GABRIEL WEATHERHEAD
  158254. 8626N
  158255. 2/28/96
  158256. A REVIEW. CHUKOVSKAYA, E. TS. THE SYNTHESIS OF SUBSTITUTED CYCLOPROPANES AND CYCLOPROPENES BY THE REDUCTIVE CYCLIZATION OF POLYCHLOROALKANES. 1982, 51, 368. RUSSIAN CHEMICAL REVIEWSa
  158257. GABRIEL WEATHERHEAD
  158258. 8627N
  158259. 2/28/96V
  158260. A REVIEW. MINKIN, V. I.; MINYAEV, R. M. POLYHEDRAL ORGANIC MOLECULES AND IONS
  158261. STRUCTURAL ANALOGUES OF ORGANOMETALLIC CLUSTERS. 1982, 51, 332. RUSSIAN CHEMICAL REVIEWSa
  158262. GABRIEL WEATHERHEAD
  158263. 8628N
  158264. 2/28/96VvA REVIEW. KHARDIN, A. P.; RADCHENKO S. S. POLYMERIC DERIVATIVES OF ADAMANTANE. 1982, 51, 272. RUSSIAN CHEMICAL REVIEWSa
  158265. GABRIEL WEATHERHEAD
  158266. 8629N
  158267. 2/28/96V
  158268. A REVIEW. PETROV, K. A.; CHAUZOV, V. A.; AGAFONOV, S. V. A ALKOXY COMPOUNDS OF PHOSPHORUS AND SOME OF THEIR ANALOGUES. 1982, 51, 234. RUSSIAN CHEMICAL REVIEWSa
  158269. GABRIEL WEATHERHEAD
  158270. 8630N
  158271. 2/28/96
  158272. A REVIEW. LYAPINA, N. K. THE PRESENT STATE OF RESEARCH INTO ORGANOSULFUR COMPOUNDS IN PETROLEUM. 1982, 51, 189. RUSSIAN CHEMICAL REVIEWSa
  158273. GABRIEL WEATHERHEAD
  158274. 8631N
  158275. 2/28/96V
  158276. A REVIEW. SHVACHKIN, YU. P.; MISHIN, G. P.; KORHSUNOVA, G. A. ADVANCES AND PROSPECTS IN THE CHEMISTRY OF NUCLEOAMINOACIDS AND NUCLEOPEPTIDES. 1982, 51,178. RUSSIAN CHEMICAL REVIEWSa
  158277. GABRIEL WEATHERHEAD
  158278. 8632N
  158279. 2/28/96V
  158280. A REVIEW. RAZVODOVSKAYA, L. V.; GRAPOV, A. F.; MEL'NIKOV, N. N. PHOSPHORYLATED AND THIOPHOSPHORYLATED AMINOHETEROCYCLES. 1982, 51, 135. RUSSIAN CHEMICAL REVIEWSa
  158281. GABRIEL WEATHERHEAD
  158282. 8633N
  158283. 2/28/96V
  158284. A REVIEW. GRANIK, V. G. INFLUENCE OF RING SIZE ON PROPERTIES AND REACTIVITY OF CYCLIC SYSTEMS. 1982, 51, 119. RUSSIAN CHEMICAL REVIEWSa
  158285. GABRIEL WEATHERHEAD
  158286. 8634N
  158287. 2/28/96
  158288. A REVIEW. GRAGEROV, I. P.; SKRUNTS, L. K.; GELLER, B. A. KINETICS AND MECHANISM OF THE OXIDATION OF ALIPHATIC AMINES. 1982, 51, 68. RUSSIAN CHEMICAL REVIEWSa
  158289. GABRIEL WEATHERHEAD
  158290. 8635N
  158291. 2/28/96V
  158292. A REVIEW. TYULENEVA, V. V.; ROKHLIN, E. M.; KNUNYANTS, I. L. FLUORINE CONTAINING PHOSPHORUS YLIDES. 1982, 51,1. RUSSIAN CHEMICAL REVIEWSa
  158293. GABRIEL WEATHERHEAD
  158294. 8636N
  158295. 2/28/96V
  158296. A REVIEW. WIERSUM, U. E. FLASH VACUUM THERMOLYSIS, A VERSATILE METHOD IN ORGANIC CHEMISTRY. PART I. GENERAL ASPECTS AND TECHNIQUES. 1982, 101, 317. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  158297. GABRIEL WEATHERHEAD
  158298. 8637N
  158299. 2/28/96V
  158300. A REVIEW. REINHOUDT, D. N. THIEPINS AND BENZOTHIEPINS; THE CONQUEST OF ELUSIVE SULFUR HETEROCYCLES. 1982,101, 277. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  158301. GABRIEL WEATHERHEAD
  158302. 8638N
  158303. 2/28/96
  158304. A REVIEW. BUCK, H. M. SPECTROPHYSICS AND PHOTOCHEMISTRY OF THE FORMALDEHYDE MOLECULE. PART II. 1982,101, 225. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  158305. GABRIEL WEATHERHEAD
  158306. 8639N
  158307. 2/28/96V
  158308. A REVIEW. DALY, J. W. ALKALOIDS OF NEOTROPICAL POISON FROGS (DENDROBATIDAE). 1982, 41, 205. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  158309. GABRIEL WEATHERHEAD
  158310. 8640N
  158311. 2/28/96VxA REVIEW. ROBINS, D. J. THE PYRROLIZIDINE ALKALOIDS. 1982, 41,115. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  158312. GABRIEL WEATHERHEAD
  158313. 8641N
  158314. 2/28/96V
  158315. A REVIEW. ROUX, D. G.; FERREIRA, D. THE DIRECT BIOMIMETIC SYNTHESIS, STRUCTURE AND ABSOLUTE CONFIGURATION OF ANGULAR AND LINEAR CONDENSED TANNINS. 1982, 41, 47. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  158316. GABRIEL WEATHERHEAD
  158317. 8642N
  158318. 2/28/96
  158319. A REVIEW. HASLAM, E. THE METABOLISM OF GALLIC ACID AND HEXAHYDROXYDIPHENIC ACID IN HIGHER PLANTS. 1982, 41,1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  158320. GABRIEL WEATHERHEAD
  158321. 8643N
  158322. 2/28/96VPA REVIEW. MUKAIYAMA, T. THE DIRECTED ALDOL REACTION. 1982, 28, ORGANIC REACTIONSa
  158323. GABRIEL WEATHERHEAD
  158324. 8644N
  158325. 2/28/96VkA REVIEW. CHENG, C. C.; YAN, S. J. THE FRIEDLANDER SYNTHESIS OF QUINOLINES. 1982, 28, 37. ORGANIC REACTIONSa
  158326. GABRIEL WEATHERHEAD
  158327. 8645N
  158328. 2/28/96V_A REVIEW. WYNBERG, H.; MEIJER, E. W. THE REIMER TIEMANN REACTION. 1982, 28,1. ORGANIC REACTIONSa
  158329. GABRIEL WEATHERHEAD
  158330. 8646N
  158331. 2/28/96V
  158332. A REVIEW. ROBINS, R. K. PURINE NUCLEOSIDE 3',5' CYCLIC MONOPHOSPHATES AS HORMONAL MODULATORS OF CELLULAR PROLIFERATION, METASTASES, AND LYMPHOCYTE RESPONSE. 1982,1, 204. NUCLEOSIDES AND NUCLEOTIDESa
  158333. GABRIEL WEATHERHEAD
  158334. 8647N
  158335. 2/28/96
  158336. A REVIEW.  ROBINS, R. K. NUCLEOSIDE AND NUCLEOTIDE INHIBITORS OF INOSINE MONOPHOSPHATE (IMP) DEHYDROGENASE AS POTENTIAL ANTITUMOR AGENTS. 1982,1, 35. NUCLEOSIDES AND NUCLEOTIDESa
  158337. GABRIEL WEATHERHEAD
  158338. 8648N
  158339. 2/28/96V
  158340. A REVIEW.  BERGSTROM, D. E. ORGANOMETALLIC INTERMEDIATES IN THE SYNTHESIS OF NUCLEOSIDE ANALOGS. 1982,1, 1. NUCLEOSIDES AND NUCLEOTIDESa
  158341. GABRIEL WEATHERHEAD
  158342. 8649N
  158343. 2/28/96V
  158344. A REVIEW. BESTMANN, H. J.; SCHMID, G.; KISIELOWSKI, L. SYNTHESIS OF THREE MEMBERED RINGS BY MEANS OF PHOSPHORUS YLIDES. 1982, 22, 45. ISRAEL JOURNAL OF CHEMISTRYa
  158345. GABRIEL WEATHERHEAD
  158346. 8650N
  158347. 2/28/96V
  158348. A REVIEW. QUAST, H.; FUSS, A. PHOTOLYSIS OF SATURATED FOUR MEMBERED RINGS WITH TWO EXOCYCLIC DOUBLE BONDS  A PHOTOEXTRUSION ROUTE TO (HETERO)METHYLENECYCLOPROPANES. 1982, 22, 31. ISRAEL JOURNAL OF CHEMISTRYa
  158349. GABRIEL WEATHERHEAD
  158350. 8651N
  158351. 2/28/96
  158352. A REVIEW. THUMMEL, R. P. THE EFFECT OF RING STRAIN ON ORTHO ANNELATED AROMATIC MOLECULES. 1982, 22,11. ISRAEL JOURNAL OF CHEMISTRYa
  158353. GABRIEL WEATHERHEAD
  158354. 8652N
  158355. 2/28/96V
  158356. A REVIEW.  KANEKO, C., NAITO, T. SYNTHESES AND REACTIONS OF CYCLOBUTANE FUSED SIX MEMBERED HETEROAROMATICS. 1982,19, 2183 HETEROCYCLESa
  158357. GABRIEL WEATHERHEAD
  158358. 8653N
  158359. 2/28/96V
  158360. A REVIEW.  BLONDET, D.; MORIN, C. SYNTHESIS AND REACTIVITY OF 2 AZABICYCLO[2.2.1]HEPTANES. HEPTENES AND HEPTADIENES. 1982, 19, 2155. HETEROCYCLESa
  158361. GABRIEL WEATHERHEAD
  158362. 8654N
  158363. 2/28/96V
  158364. A REVIEW. BOX, V. G. S. SOME CONSEQUENCES OF LONE PAIR INTERACTIONS IN THE CHEMISTRY OF MONOSACCHARIDES. 1982,19 1939. HETEROCYCLESa
  158365. GABRIEL WEATHERHEAD
  158366. 8655N
  158367. 2/28/96VfA REVIEW. PIANCATELLI, G. ADVANCES IN CYCLOPENTENONE SYNTHESIS FROM FURANS. 1982,19,1735. HETEROCYCLESa
  158368. GABRIEL WEATHERHEAD
  158369. 8656N
  158370. 2/28/96
  158371. TViA REVIEW. WITCZAK, Z. J.; WHISTLER, R. L. CARBOHYDRATES CONTAINING SELENIUM. 1982, 19, 1719. HETEROCYCLESa
  158372. GABRIEL WEATHERHEAD
  158373. 8657N
  158374. 2/28/96VHA REVIEW. ONG, C. W. TRICHOTHECANES
  158375. A REVIEW. 1982,19,1685. HETEROCYCLESa
  158376. GABRIEL WEATHERHEAD
  158377. 8658N
  158378. 2/28/96VqA REVIEW. PELTER, A. CARBON CARBON BOND FORMATION INVOLVING BORON REAGENTS. 1982,11,191. CHEMICAL SOCIETY REVIEWSa
  158379. GABRIEL WEATHERHEAD
  158380. 8659N
  158381. 2/28/96VoA REVIEW. TROST, B. M. CYCLOPENTANOIDS: A CHALLENGE FOR NEW METHODOLOGY. 1982,11, 141. CHEMICAL SOCIETY REVIEWSa
  158382. GABRIEL WEATHERHEAD
  158383. 8660N
  158384. 2/28/96VmA REVIEW. LIU, M. T. H. THE THERMOLYSIS AND PHOTOLYSIS OF DIAZIRINES. 1982, 11, 127. CHEMICAL SOCIETY REVIEWSa
  158385. GABRIEL WEATHERHEAD
  158386. 8661N
  158387. 2/28/96VeA REVIEW. WARD, R. S. THE SYNTHESIS OF LIGNANS AND NEOLIGNANS. 1982, 11, 75. CHEMICAL SOCIETY REVIEWSa
  158388. GABRIEL WEATHERHEAD
  158389. 8662N
  158390. 2/28/96
  158391. ZVmA REVIEW. HOLLAND, H. L. METHYL GROUP REMOVAL IN STEROID BIOSYNTHESIS. 1981,10, 435. CHEMICAL SOCIETY REVIEWSa
  158392. GABRIEL WEATHERHEAD
  158393. 8663N
  158394. 2/28/96VeA REVIEW. LINDBERG, B. STRUCTURAL STUDIES OF POLYSACCHARIDES. 1981, 10, 409. CHEMICAL SOCIETY REVIEWSa
  158395. GABRIEL WEATHERHEAD
  158396. 8664N
  158397. 2/28/96V^A REVIEW.  VARVOGLIS, A. ARYLIODINE(III) DICARBOXYLATES. 1981,10, 377 CHEMICAL SOCIETY REVIEWSa
  158398. GABRIEL WEATHERHEAD
  158399. 8665N
  158400. 2/28/96VhA REVIEW. JENCKS, W. P. HOW DOES A REACTION CHOOSE ITS MECHANISM? 1981,10, 345. CHEMICAL SOCIETY REVIEWSa
  158401. GABRIEL WEATHERHEAD
  158402. 8666N
  158403. 2/28/96V
  158404. A REVIEW. JONES, J. R.; TAYLOR, S. E. ISOTOPIC HYDROGEN EXCHANGE IN PURINES
  158405. MECHANISMS AND APPLICATIONS. 1981,10, 329. CHEMICAL SOCIETY REVIEWSa
  158406. GABRIEL WEATHERHEAD
  158407. 8667N
  158408. 2/28/96V}A REVIEW.  MOORE, H. W.; GHEORGHIU, M. D. CYANOKETENES: SYNTHESIS AND CYCLOADDITIONS. 1981, 10, 289. CHEMICAL SOCIETY REVIEWS
  158409. GABRIEL WEATHERHEAD
  158410. 8668N
  158411. 2/28/96V
  158412. A REVIEW. MUETTERTIES, E. L.; BLEEKE, J. R.; WUCHERER, E. J., ALBRIGHT T. A. STRUCTURAL, STEREOCHEMICAL, AND ELECTRONIC FEATURES OF ARENE METAL COMPLEXES. 1982, 82, 499. CHEMICAL REVIEWSa
  158413. GABRIEL WEATHERHEAD
  158414. 8669N
  158415. 2/28/96V
  158416. A REVIEW. ARTAMKINA, G. A.; EGOROV, M. P.; BELETSKAYA, 1. P. SOME ASPECTS OF ANIONIC S COMPLEXES. 1982, 82, 427. CHEMICAL REVIEWSa
  158417. GABRIEL WEATHERHEAD
  158418. 8670N
  158419. 2/28/96VhA REVIEW. KUTNEY, G. W.; TURNBULL, K. COMPOUNDS CONTAINING THE S=S BOND. 1982, 82, 333. CHEMICAL REVIEWSa
  158420. GABRIEL WEATHERHEAD
  158421. 8671N
  158422. 2/28/96VVA REVIEW.  HOLDER, N. L. THE CHEMISTRY OF HEXENULOSES. 1982, 82, 287. CHEMICAL REVIEWSa
  158423. GABRIEL WEATHERHEAD
  158424. 8672N
  158425. 2/28/96
  158426. A REVIEW. DEMUTH, M.; SCHAFFNER, K. TRICYCLO[3.3.0.02,8]OCTAN 3 ONES: PHOTOCHEMICALLY PREPARED BUILDING BLOCKS FOR ENANTIOSPECIFIC TOTAL SYNTHESES OF CYCLOPENTANOID NATURAL PRODUCTS. 1982, 21, 820. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158427. GABRIEL WEATHERHEAD
  158428. 8673N
  158429. 2/28/96V
  158430. A REVIEW. UGI, I. FROM ISOCYANIDES UIA  FOUR COMPONENT CONDENSATIONS TO ANTIBIOTIC SYNTHESES. 1982, 21, 810. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158431. GABRIEL WEATHERHEAD
  158432. 8674N
  158433. 2/28/96V
  158434. A REVIEW. FUKUI, K. THE ROLE OF FRONTIER ORBITALS IN CHEMICAL REACTIONS (NOBEL LECTURE). 1982, 21, 801. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158435. GABRIEL WEATHERHEAD
  158436. 8675N
  158437. 2/28/96V
  158438. A REVIEW. BARTMANN, W.; BECK, G. PROSTACYCLIN AND SYNTHETIC ANALOGUES. 1982, 21, 751. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158439. GABRIEL WEATHERHEAD
  158440. 8676N
  158441. 2/28/96
  158442. A REVIEW. MIMOUN, H. OXYGEN TRANSFER FROM INORGANIC AND ORGANIC PEROXIDES TO ORGANIC SUBSTRATES: A COMMON MECHANISM? 1982, 21, 734. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158443. GABRIEL WEATHERHEAD
  158444. 8677N
  158445. 2/28/96V
  158446. A REVIEW. HOFFMANN, R. BUILDING BRIDGES BETWEEN INORGANIC AND ORGANIC CHEMISTRY (NOBEL LECTURE). 1982, 21, 711. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158447. GABRIEL WEATHERHEAD
  158448. 8678N
  158449. 2/28/96V
  158450. A REVIEW. PUSCH, W.; WATCH, A. SYNTHETIC MEMBRANES
  158451.  PREPARATION, STRUCTURE, AND APPLICATION. 1982, 21, 660. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158452. GABRIEL WEATHERHEAD
  158453. 8679N
  158454. 2/28/96V
  158455. A REVIEW. SEEBACH, D.; PRELOG, V. THE UNAMBIGUOUS SPECIFICATION OF THE STERIC COURSE OF ASYMMETRIC SYNTHESES. 1982, 21, 654. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158456. GABRIEL WEATHERHEAD
  158457. 8680N
  158458. 2/28/96
  158459. A REVIEW. JAENICKE, L., BOLAND, W. SIGNAL SUBSTANCES AND THEIR RECEPTION IN THE SEXUAL CYCLE OF MARINE BROWN ALGAE. 1982, 21, 643. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158460. GABRIEL WEATHERHEAD
  158461. 8681N
  158462. 2/28/96V
  158463. A REVIEW. DRAUZ, K., KLEEMANN, A., MARTENS, J. INDUCTION OF ASYMMETRY BY AMINO ACIDS. 1982, 21, 584. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158464. GABRIEL WEATHERHEAD
  158465. 8682N
  158466. 2/28/96V
  158467. A REVIEW.  PRELOG, V., HELMCHEN, H. BASIC PRINCIPLES OF THE CIP SYSTEM AND PROPOSALS FOR A REVISION. 1982, 21, 567. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158468. GABRIEL WEATHERHEAD
  158469. 8683N
  158470. 2/28/96V
  158471. A REVIEW. HOFFMANN, R. W. DIASTEREOGENIC ADDITION OF CROTYLMETAL COMPOUNDS TO ALDEHYDES. 1982, 21, 555. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158472. GABRIEL WEATHERHEAD
  158473. 8684N
  158474. 2/28/96
  158475. A REVIEW. J KESSLER, H. CONFORMATION AND BIOLOGICAL ACTIVITY OF CYCLIC PEPTIDES. 1982, 2I, 512. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158476. GABRIEL WEATHERHEAD
  158477. 8685N
  158478. 2/28/96V
  158479. A REVIEW. BAUDLER, M. CHAIN AND RING PHOSPHORUS COMPOUNDS
  158480.  ANALOGIES BETWEEN PHOSPHORUS AND CARBON CHEMISTRY. L982, 21, 492. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158481. GABRIEL WEATHERHEAD
  158482. 8686N
  158483. 2/28/96V
  158484. A REVIEW. HARRE, M.; RADDATZ, P.; WALENTA, R.; WINTERFELDT, E. 4 0XO 2 CYCLOPENTENYL ACETATE
  158485. A SYNTHETIC INTERMEDIATE. 1982, 21, 480. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158486. GABRIEL WEATHERHEAD
  158487. 8687N
  158488. 2/28/96V
  158489. A REVIEW.  KLEINSCHROTH, J.; HOPF, H. THE CHEMICAL BEHAVIOR OF MULTIBRIDGED [2N]CYCLOPHANES. 1982, 21, 469. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158490. GABRIEL WEATHERHEAD
  158491. 8688N
  158492. 2/28/96
  158493. A REVIEW.  TEDDER, J. M. WHICH FACTORS DETERMINE THE REACTIVITY AND REGIOSELECTIVITY OF FREE RADICAL SUBSTITUTION AND ADDITION REACTIONS? 1982, 21, 401. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158494. GABRIEL WEATHERHEAD
  158495. 8689N
  158496. 2/28/96V
  158497. A REVIEW. SIGEL, H. HYDROPHOBIC AND METAL ION COORDINATING PROPERTIES OF A LIPOIC ACID
  158498. AN EXAMPLE OF INTRAMOLECULAR EQUILIBRIA IN METAL ION COMPLEXES. 1982, 21, 389. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  158499. GABRIEL WEATHERHEAD
  158500. 8690N
  158501. 2/28/96V
  158502. A REVIEW. HASE, T. A.; KOSKIMIES, J. K. A COMPILATION OF REFERENCES ON R FUNCTIONAL ACYL ANION SYNTHONS, RCO . 1982, 2, 35. ALDRICHIMICA ACTAa
  158503. GABRIEL WEATHERHEAD
  158504. 8691N
  158505. 2/28/96V
  158506. A REVIEW. EVANS, D. A. STUDIES IN ASYMMETRIC SYNTHESIS. THE DEVELOPMENT OF PRACTICAL CHIRAL ENOLATE SYNTHONS. 1982, 2, 23. ALDRICHIMICA ACTAa
  158507. GABRIEL WEATHERHEAD
  158508. 8692N
  158509. 2/28/96
  158510. xVtA REVIEW. DEAN, F. M. RECENT ADVANCES IN FURAN CHEMISTRY. PART II. 1982, 31, 238. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158511. GABRIEL WEATHERHEAD
  158512. 8693N
  158513. 2/28/96V
  158514. A REVIEW.  METH COHN, O., TARNOWSKI, B. CYCLIZATIONS UNDER VILSMEIER CONDITIONS. 1982, 31, 207. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158515. GABRIEL WEATHERHEAD
  158516. 8694N
  158517. 2/28/96V
  158518. A REVIEW. KOBAYASHI, Y., KUMADAKI, I. DEWAR HETEROCYCLES AND RELATED COMPOUNDS. 1982, 31,169. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158519. GABRIEL WEATHERHEAD
  158520. 8695N
  158521. 2/28/96VhA REVIEW. PERLMUTTER, H. D.; TRATTNER, R. B. AZOCINES. 1982, 31, 116. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158522. GABRIEL WEATHERHEAD
  158523. 8696N
  158524. 2/28/96VzA REVIEW. PEDERSEN, C. TH. 1,2 DITHIOLE 3 THIONES AND 1,2 DITHIOL 3 ONES. 1982, 31, 63. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158525. GABRIEL WEATHERHEAD
  158526. 8697N
  158527. 2/28/96
  158528. }V[A REVIEW.  JONES, G. AROMATIC QUINOLIZINES. 1982, 31, 2. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  158529. GABRIEL WEATHERHEAD
  158530. 8698N
  158531. 2/28/96V}A REVIEW. BUTLER, G. B. CYCLOPOLYMERIZATION AND CYCLOCOPOLYMERIZATION. 1982, 15, 370. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158532. GABRIEL WEATHERHEAD
  158533. 8699N
  158534. 2/28/96V
  158535. A REVIEW. STANG, P. J. RECENT DEVELOPMENTS IN UNSATURATED CARBENES AND RELATED CHEMISTRY. 1982,15, 348. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158536. GABRIEL WEATHERHEAD
  158537. 8700N
  158538. 2/28/96V
  158539. A REVIEW. NEGISHI, E. I. PALLADIUM  OR NICKEL CATALYZED CROSS COUPLING. A NEW SELECTIVE METHOD FOR CARBON CARBON BOND FORMATION. 1982,15, 340. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158540. GABRIEL WEATHERHEAD
  158541. 8701N
  158542. 2/28/96V
  158543. A REVIEW. HALPERN, J. FORMATION OF CARBON HYDROGEN BONDS BY REDUCTIVE ELIMINATION. 1982,15, 332. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158544. GABRIEL WEATHERHEAD
  158545. 8702N
  158546. 2/28/96
  158547. A REVIEW.  ZIMMERMAN, H. E. SOME THEORETICAL ASPECTS OF ORGANIC PHOTOCHEMISTRY. 1982, 15, 312. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158548. GABRIEL WEATHERHEAD
  158549. 8703N
  158550. 2/28/96V
  158551. A REVIEW. BEAK, P.; SNIECKUS, V. DIRECTED LITHIATION OF AROMATIC TERTIARY AMIDES: AN EVOLVING SYNTHETIC METHODOLOGY FOR POLYSUBSTITUTED AROMATICS. 1982,15, 306. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158552. GABRIEL WEATHERHEAD
  158553. 8704N
  158554. 2/28/96V
  158555. A REVIEW.  PARHAM, W. E.; BRADSHER, C. K. AROMATIC ORGANOLITHIUM REAGENTS BEARING ELECTROPHILIC GROUPS. PREPARATION BY HALOGEN LITHIUM EXCHANGE. 1982,15, 300. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158556. GABRIEL WEATHERHEAD
  158557. 8705N
  158558. 2/28/96V|A REVIEW.  GANEM, B. NEW CHEMISTRY OF NATURALLY OCCURRING POLYAMINES. 1982, 15, 290. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158559. GABRIEL WEATHERHEAD
  158560. 8706N
  158561. 2/28/96
  158562. A REVIEW. SCHAEFER, H. F., III THE SILICON CARBON DOUBLE BOND: A HEALTHY RIVALRY BETWEEN THEORY AND EXPERIMENT. 1982, 15, 283. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158563. GABRIEL WEATHERHEAD
  158564. 8707N
  158565. 2/28/96V
  158566. A REVIEW. KOSOWER, E. M. INTRAMOLECULAR DONOR ACCEPTOR SYSTEMS. 9. EXCITED STATE INTRAMOLECULAR CHARGE TRANSFER. 1982, 15, 259. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158567. GABRIEL WEATHERHEAD
  158568. 8708N
  158569. 2/28/96V
  158570. A REVIEW. SCAIANO, J. C. LASER FLASH PHOTOLYSIS STUDIES OF THE REACTIONS OF SOME 1,4 BIRADICALS. 1982,15, 262. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158571. GABRIEL WEATHERHEAD
  158572. 8709N
  158573. 2/28/96V
  158574. A REVIEW. PADDON ROW, M. N. SOME ASPECTS OF ORBITAL INTERACTIONS THROUGH BONDS: PHYSICAL AND CHEMICAL CONSEQUENCES. 1982, Z5, 245. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158575. GABRIEL WEATHERHEAD
  158576. 8710N
  158577. 2/28/96
  158578. VvA REVIEW. LIPSCOMB, W. N. ACCELERATION OF REACTIONS BY ENZYMES. 1982, 15, 232. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158579. GABRIEL WEATHERHEAD
  158580. 8711N
  158581. 2/28/96V
  158582. A REVIEW. LYERLA, J. R.; YANNONI, C. S.; FYFE, C. A. CHEMICAL APPLICATIONS OF VARIABLE TEMPERATURE CPMAS NMR SPECTROSCOPY IN SOLIDS. 1982, 15, 208. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  158583. GABRIEL WEATHERHEAD
  158584. 8712N
  158585. 2/28/96V\A REVIEW.  WARREN, S. ORGANIC SYNTHESIS: THE DISCONNECTION APPROACH. WILEY: NEWJERSEY, 1982.a
  158586. GABRIEL WEATHERHEAD
  158587. 8713N
  158588. 2/28/96VcA REVIEW. TOUCHSTONE, J. C. PRACTICE OF THIN LAYER CHROMATOGRAPHY, 2ND ED. WILEY: NEW JERSEY, 1983.a
  158589. GABRIEL WEATHERHEAD
  158590. 8714N
  158591. 2/28/96VYA REVIEW.  ROBINSON, B. THE FISCHER INDOLE SYNTHESIS. WILEY INTERSCIENCE: NEW YORK, 1982.a
  158592. GABRIEL WEATHERHEAD
  158593. 8715N
  158594. 2/28/96
  158595. A REVIEW. RETEY, J.; ROBINSON, J. A. STEREOSPECIFICITY IN ORGANIC CHEMISTRY AND ENZYMOLOGY, VOLUME 13. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1982.a
  158596. GABRIEL WEATHERHEAD
  158597. 8716N
  158598. 2/28/96VoA REVIEW.  PELLETIER, S. W. ALKALOIDS. CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOLUME 1. WILEY: NEW JERSEY, 1983.a
  158599. GABRIEL WEATHERHEAD
  158600. 8717N
  158601. 2/28/96V
  158602. A REVIEW. ROSSI, R. A.; DE ROSSI, R. H. AROMATIC SUBSTITUTION BY THE SRN1 MECHANISM. AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, 1983.a
  158603. GABRIEL WEATHERHEAD
  158604. 8718N
  158605. 2/28/96VUA REVIEW. PETTIT, G. R. SYNTHETIC PEPTIDES, VOLUME 6. ACADEMIC PRESS: NEW YORK, 1982.a
  158606. GABRIEL WEATHERHEAD
  158607. 8719N
  158608. 2/28/96V
  158609. A REVIEW. MARSHALL J. L. CARBON CARBON AND CARBON PROTON NMR COUPLINGS: APPLICATIONS TO ORGANIC STEREOCHEMISTRY AND CONFORMATIONAL ANALYSIS, VOLUMES 2. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1982.a
  158610. GABRIEL WEATHERHEAD
  158611. 8720N
  158612. 2/28/96
  158613. A REVIEW.  MARCHAND, A. P. STEREOCHEMICAL APPLICATIONS OF NMR STUDIES IN RIGID BICYCLIC SYSTEMS, VOLUME 1. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1982.a
  158614. GABRIEL WEATHERHEAD
  158615. 8721N
  158616. 2/28/96VBA REVIEW. HIRAOKA, M. CROWN COMPOUNDS. KODANSHA LTD.: TOKYO, 1982.a
  158617. GABRIEL WEATHERHEAD
  158618. 8722N
  158619. 2/28/96VlA REVIEW. BURKERT, U.; ALLINGER, N. L. MOLECULAR MECHANICS. AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1982.a
  158620. GABRIEL WEATHERHEAD
  158621. 8723N
  158622. 2/28/96V
  158623. A REVIEW. BERDY, J. CRC HANDBOOK OF ANTIBIOTIC COMPOUNDS VOLUMES V VII (1981); VOLUMES VIII X (1982). CRC PRESS BOCA RATON, FL.a
  158624. GABRIEL WEATHERHEAD
  158625. 8724N
  158626. 2/28/96V
  158627. A REVIEW. BUNDS, R. E. PREPARATION, PROPERTIES, AND INDUSTRIAL APPLICATIONS OF ORGANOFLUORINE COMPOUNDS. WILEY: NEW JERSEY, 1982.a
  158628. GABRIEL WEATHERHEAD
  158629. 8725N
  158630. 2/28/96VeA REVIEW. BAERHEIM SVENDSEN, A.; VERPOORTE, R. CHROMATOGRAPHY OF ALKALOIDS. ELSEVIER: NEW YORK, 1983.
  158631. GABRIEL WEATHERHEAD
  158632. 8726N
  158633. 2/28/96V}A REVIEW. RAPPOPORT, Z. VINYL CATIONS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158634. GABRIEL WEATHERHEAD
  158635. 8727N
  158636. 2/28/96V
  158637. A REVIEW. BRUN, P.; WAEGALL, B. SYNTHETIC APPLICATIONS AND REACTIVITY OF ALKOXYL RADICALS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158638. GABRIEL WEATHERHEAD
  158639. 8728N
  158640. 2/28/96V
  158641. A REVIEW. SZEIMIES, G. BRIDGEHEAD OLEFINS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158642. GABRIEL WEATHERHEAD
  158643. 8729N
  158644. 2/28/96V
  158645. A REVIEW. BENTRUDE, W. G. PHOSPHORANYL RADICALS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158646. GABRIEL WEATHERHEAD
  158647. 8730N
  158648. 2/28/96
  158649. A REVIEW. WILT, J. W. RADICAL REACTIONS OF SILANES. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158650. GABRIEL WEATHERHEAD
  158651. 8731N
  158652. 2/28/96V
  158653. A REVIEW. TIECCO, M.; TESTAFERRI, L. HOMOLYTIC AROMATIC SUBSTITUTION BY ALKYL RADICALS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 3. 1982a
  158654. GABRIEL WEATHERHEAD
  158655. 8732N
  158656. 2/28/96V
  158657. A REVIEW.  BARETTA, A.; WAEGELL, B. FAVORSKII REARRANGEMENT MECHANISMS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158658. GABRIEL WEATHERHEAD
  158659. 8733N
  158660. 2/28/96V
  158661. A REVIEW.  REINECKE, M. G. FIVE MEMBERED HETARYNES. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158662. GABRIEL WEATHERHEAD
  158663. 8734N
  158664. 2/28/96
  158665. A REVIEW. TANG, Y. N. REACTIONS IN SILICON ATOMS AND SILYLENES. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158666. GABRIEL WEATHERHEAD
  158667. 8735N
  158668. 2/28/96V
  158669. A REVIEW.  SURZUR, J. M. CYCLIZATIONS BY INTRAMOLECULAR ADDITIONS. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158670. GABRIEL WEATHERHEAD
  158671. 8736N
  158672. 2/28/96V
  158673. A REVIEW. PADWA, A.; CARLSEN, J. H. J. NITRILE YLIDES AND NITRENES FROM 2H AZIRINES. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158674. GABRIEL WEATHERHEAD
  158675. 8737N
  158676. 2/28/96V
  158677. A REVIEW. SCRIVEN, E. F. V. SOLUTION CHEMISTRY OF ARYL NITRENES. REACTIVE INTERMEDIATES, R. A. ABRAMOVITCH, ED., PLENUM PRESS: NEW YORK. VOLUME 2. 1982a
  158678. GABRIEL WEATHERHEAD
  158679. 8738N
  158680. 2/28/96
  158681. A REVIEW.  ABBOUD, J. L. M.; KAMLET, M. J.; TAFT, R. W. AN EXAMINATION OF LINEAR SOLVATION ENERGY RELATIONSHIPS, P 485. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158682. GABRIEL WEATHERHEAD
  158683. 8739N
  158684. 2/28/96V
  158685. A REVIEW.  RUNGE, W. SUBSTITUENT EFFECTS IN ALLENES AND CUMULENES, P 315. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158686. GABRIEL WEATHERHEAD
  158687. 8740N
  158688. 2/28/96V
  158689. A REVIEW. STOCK, L. M.; WASIELEWSKI, M. R. THE TRIFLUOROMETHYL GROUP IN CHEMISTRY AND SPECTROSCOPY CARBON FLUORINE HYPERCONJUGATION, P 253. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158690. GABRIEL WEATHERHEAD
  158691. 8741N
  158692. 2/28/96
  158693. A REVIEW.  CHARTON, M. ELECTRICAL EFFECT SUBSTITUENT CONSTANTS FOR CORRELATION ANALYSIS P 119. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158694. GABRIEL WEATHERHEAD
  158695. 8742N
  158696. 2/28/96V
  158697. A REVIEW. GODLESKI, S. A.; SCHLEYER, P. V. R.; OSAWA, E., WIPKE, W. T. THE SYSTEMATIC PREDICTION OF THE MOST STABLE NEUTRAL HYDROCARBON ISOMER, P 63. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158698. GABRIEL WEATHERHEAD
  158699. 8743N
  158700. 2/28/96V
  158701. A REVIEW.  PROSS, A.; RADOM, L. A THEORETICAL APPROACH TO SUBSTITUENT INTERACTIONS IN SUBSTITUTED BENZENES, P 1. PROGRESS IN PHYAICAL ORGANIC CHEMISTRY, VOLUME 13, R. TAFT, ED., WILEY INTERSCIENCE: NEW YORK, 1983.a
  158702. GABRIEL WEATHERHEAD
  158703. 8744N
  158704. 2/28/96
  158705. A REVIEW. JOHANSEN, J. T. ENZYMATIC SYNTHESIS OF PEPTIDES. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158706. GABRIEL WEATHERHEAD
  158707. 8745N
  158708. 2/28/96V
  158709. A REVIEW.  ROBERTS, D. C.; VELLACCIO, F. UNUSUAL AMINO ACIDS IN PEPTIDE SYNTHESIS. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158710. GABRIEL WEATHERHEAD
  158711. 8746N
  158712. 2/28/96V
  158713. A REVIEW. NODA, K.; SHIMOHIGASHI, Y.; IZUMIYA, N. A,B DEHYDROPEPTIDES. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158714. GABRIEL WEATHERHEAD
  158715. 8747N
  158716. 2/28/96
  158717. A REVIEW. BENOITON, N. L. QUANTITATION AND SEQUENCE DEPENDENCE OF RACEMIZATION IN PEPTIDE SYNTHESIS. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.
  158718. GABRIEL WEATHERHEAD
  158719. 8748N
  158720. 2/28/96V
  158721. A REVIEW. BODANSZKY, M.; MARTINEZ, J. SIDE REACTIONS IN PEPTIDE SYNTHESIS. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158722. GABRIEL WEATHERHEAD
  158723. 8749N
  158724. 2/28/96V
  158725. A REVIEW. YAJIMA, H.; JUJII, M. ACIDOLYTIC DEPROTECTION PROCEDURES IN PEPTIDE SYNTHESIS. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158726. GABRIEL WEATHERHEAD
  158727. 8750N
  158728. 2/28/96
  158729. A REVIEW. WETZEL R., GOEDDEL, D. V. SYNTHESIS OF POLYPEPTIDES BY RECOMBINANT DNA METHODS. THE PEPTIDES. ANALYSIS, SYNTHESIS, BIOLOGY, VOLUME 5, SPECIAL METHODS IN PEPTIDE SYNTHESIS, E. GROSS AND J. MEIENHOFER, EDS., ACADEMIC PRESS: NEW YORK, 1983.a
  158730. GABRIEL WEATHERHEAD
  158731. 8751N
  158732. 2/28/96V
  158733. A REVIEW. CRISTOL, S.; BINDEL, T. A. PHOTOSOLVOLYSES AND ATTENDANT PHOTOREACTIONS INVOLVING CARBOCATIONS. ORGANIC PHOTOCHEMISTRY, VOLUME 6, A. PADWA, ED., MARCELL DEKKER: NEW YORK, 1983.a
  158734. GABRIEL WEATHERHEAD
  158735. 8752N
  158736. 2/28/96V
  158737. A REVIEW. FARID, S., MATTES, S. L. PHOTOCHEMICAL ELECTRON TRANSFER REACTIONS OF OLEFINS AND RELATED COMPOUNDS. ORGANIC PHOTOCHEMISTRY, VOLUME 6, A. PADWA, ED., MARCELL DEKKER: NEW YORK, 1983.a
  158738. GABRIEL WEATHERHEAD
  158739. 8753N
  158740. 2/28/96V
  158741. A REVIEW. TOLBERT, L. M. THE PHOTOCHEMISTRY OF ORGANIC ANIONS. ORGANIC PHOTOCHEMISTRY, VOLUME 6, A. PADWA, ED., MARCELL DEKKER: NEW YORK, 1983.a
  158742. GABRIEL WEATHERHEAD
  158743. 8754N
  158744. 2/28/96V
  158745. A REVIEW.  SUNDBERG, R. J. CHLOROACETAMIDE PHOTOCYCLIZATIONS AND OTHER AROMATIC ALKYLATIONS INITIATED BY PHOTO INDUCED ELECTRON TRANSFER. ORGANIC PHOTOCHEMISTRY, VOLUME 6, A. PADWA, ED., MARCELL DEKKER: NEW YORK, 1983.a
  158746. GABRIEL WEATHERHEAD
  158747. 8755N
  158748. 2/28/96V
  158749. A REVIEW. SCHULTZ, A. G.; MOTYKA, L. PHOTOCHEMICAL HETEROCYCLIZATIONS OF SYSTEMS ISOELECTRONIC WITH PENTADIENYL ANION. ORGANIC PHOTOCHEMISTRY, VOLUME 6, A. PADWA, ED., MARCELL DEKKER: NEW YORK, 1983.a
  158750. GABRIEL WEATHERHEAD
  158751. 8756N
  158752. 2/28/96V
  158753. A REVIEW. ZOLLER, V. THREE MEMBERED RINGS CONTAINING SULFUR. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 1, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983. THIIRANES THIIRENESa
  158754. GABRIEL WEATHERHEAD
  158755. 8757N
  158756. 2/28/96V
  158757. A REVIEW.  NAIR, V. AZIRINES. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 1, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158758. GABRIEL WEATHERHEAD
  158759. 8758N
  158760. 2/28/96V
  158761. A REVIEW. DEYRUP, J. A. AZIRIDINES. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 1, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158762. GABRIEL WEATHERHEAD
  158763. 8759N
  158764. 2/28/96V
  158765. A REVIEW.  COLLINS, M. A. MAMMALIAN ALKALOIDS. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158766. GABRIEL WEATHERHEAD
  158767. 8760N
  158768. 2/28/96V
  158769. A REVIEW. LUNDSTROM, J. SIMPLE ISOQUINOLINE ALKALOIDS. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158770. GABRIEL WEATHERHEAD
  158771. 8761N
  158772. 2/28/96V
  158773. A REVIEW.  WITKOP, B.; COSSINGER, E. AMPHIBIAN ALKALOIDS. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158774. GABRIEL WEATHERHEAD
  158775. 8762N
  158776. 2/28/96
  158777. A REVIEW. ARAL, T.; KUBO, A. ISOQUINOLINEQUINONES FROM ACTINOMYCETES AND SPONGES. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983. 1 155a
  158778. GABRIEL WEATHERHEAD
  158779. 8763N
  158780. 2/28/96V
  158781. A REVIEW. BERGMAN, J. THE QUINAZOLINOCARBOLINE ALKALOIDS. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158782. GABRIEL WEATHERHEAD
  158783. 8764N
  158784. 2/28/96V
  158785. A REVIEW. GERZON K.; SVOBODA, G. H. ACRIDONE ALKALOIDS: EXPERIMENTAI ANTITUMOR ACTIVITY OF ACRONYCINE. THE ALKALOIDS, VOLUME 21. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  158786. GABRIEL WEATHERHEAD
  158787. 8765N
  158788. 2/28/96V
  158789. A REVIEW. HAUBENSTOCK, H. ASYMMETRIC REDUCTIONS WITH CHIRAL COMPLEX ALUMINUM HYDRIDES AND TRICOORDINNTE ALUMINUM REAGENTS. 1983,14, 213. TOPICS IN STEREOCHEMISTRYa
  158790. GABRIEL WEATHERHEAD
  158791. 8766N
  158792. 2/28/96
  158793. VzA REVIEW. HIRSCHMANN, H.; HANSON, K. R. ON FACTORING CHIRALITY AND STEREOISOMERISM. 1983,14,183. TOPICS IN STEREOCHEMISTRYa
  158794. GABRIEL WEATHERHEAD
  158795. 8767N
  158796. 2/28/96V
  158797. A REVIEW. SANDSTROM, J. STATIC AND DYNAMIC STEREOCHEMISTRY OF PUSH PULL AND STRAINED ETHYLENES. 1983,14, 83. TOPICS IN STEREOCHEMISTRYa
  158798. GABRIEL WEATHERHEAD
  158799. 8768N
  158800. 2/28/96VYA REVIEW. OKI, M. RECENT ADVANCES IN ATROPISOMERISM. 1983,14, 1 TOPICS IN STEREOCHEMISTRYa
  158801. GABRIEL WEATHERHEAD
  158802. 8769N
  158803. 2/28/96VyA REVIEW. PILLAI, V. N. R. NEW PERSPECTIVES IN POLYMER SUPPORTED PEPTIDE SYNTHESIS. 1982,106. TOPICS IN CURRENT CHEMISTRYa
  158804. GABRIEL WEATHERHEAD
  158805. 8770N
  158806. 2/28/96V
  158807. A REVIEW. MAJECTIC, V. K.; NEWKOME, G. R. PYRIDINOPHANES, PYRIDINOCROWNS, AND PYRIDOCRYPTANDS. 1982,106. TOPICS IN CURRENT CHEMISTRYa
  158808. GABRIEL WEATHERHEAD
  158809. 8771N
  158810. 2/28/96
  158811. A REVIEW.  SIGEL, H. J. LITHIUM HALOCARBENOIDS. CARBANIONS OF HIGH SYNTHETIC VERSATILITY. 1982,106. TOPICS IN CURRENT CHEMISTRYa
  158812. GABRIEL WEATHERHEAD
  158813. 8772N
  158814. 2/28/96V
  158815. A REVIEW. REETZ, M. T. ORGANOTITANIUM REAGENTS IN ORGANIC SYNTHESIS. A SIMPLE MEANS TO ADJUST REACTIVITY AND SELECTIVITY OF CARBANIONS. 1982,106. TOPICS IN CURRENT CHEMISTRYa
  158816. GABRIEL WEATHERHEAD
  158817. 8773N
  158818. 2/28/96V
  158819. A REVIEW. ASHE, A. J., III. THE GROUP 5 HETEROBENZENES
  158820.  ARSABENZENE, STIBABENZENE AND BISMABENZENE. 1982,105. TOPICS IN CURRENT CHEMISTRYa
  158821. GABRIEL WEATHERHEAD
  158822. 8774N
  158823. 2/28/96VeA REVIEW. CONSIGLIO, G.; PINO, P. ASYMMETRIC HYDROFORMYLATION. 1982, 105. TOPICS IN CURRENT CHEMISTRYa
  158824. GABRIEL WEATHERHEAD
  158825. 8775N
  158826. 2/28/96VaA REVIEW.  ELIEL, E. L. PROSTEREOISOMERISM (PROCHIRALITY). 1982, 105. TOPICS IN CURRENT CHEMISTRYa
  158827. GABRIEL WEATHERHEAD
  158828. 8776N
  158829. 2/28/96
  158830. A REVIEW. RZAEV, Z. M. 0. COORDINATION EFFECTS IN FORMATION AND CROSS LINKING RENCTIONS OF ORGANOTIN MACROMOLECULES. 1982, 104. TOPICS IN CURRENT CHEMISTRYa
  158831. GABRIEL WEATHERHEAD
  158832. 8777N
  158833. 2/28/96V
  158834. A REVIEW. GIELEN, M. CHIRALITY, STATIC AND DYNAMIC STEREOCHEMISTRY OF ORGANOTIN COMPOUNDS. 1982,104. TOPICS IN CURRENT CHEMISTRYa
  158835. GABRIEL WEATHERHEAD
  158836. 8778N
  158837. 2/28/96V
  158838. A REVIEW. VEITH, M.; RECKTENWAL, 0. STRUCTURE AND REACTIVITY OF MONOMERIC, MOLECULAR TIN(II) COMPOUNDS. 1982, 104. TOPICS IN CURRENT CHEMISTRYa
  158839. GABRIEL WEATHERHEAD
  158840. 8779N
  158841. 2/28/96V
  158842. A REVIEW. RAO, A. S., PAKNIKAR, S. K., KIRTANE, J. G. RECENT ADVNNCES IN THE PREPARATION OF SYNTHETIC APPLICATIONS OF OXIRANES. 1983, 39, 2323. TETRAHEDRONa
  158843. GABRIEL WEATHERHEAD
  158844. 8780N
  158845. 2/28/96V~A REVIEW. GINSBURG, D. THE ROLE OF SECONDARY ORBITAL INTERACTIONS IN CONTROL OF ORGANIC REACTIONS. 1983, 39, 2095. TETRAHEDRONa
  158846. GABRIEL WEATHERHEAD
  158847. 8781N
  158848. 2/28/96VPA REVIEW. GREEN, R. H.; LAMBETH, P. F. LEUKOTRIENES. 1983, 39, 1687. TETRAHEDRONa
  158849. GABRIEL WEATHERHEAD
  158850. 8782N
  158851. 2/28/96VrA REVIEW.  CROFT, A. P.; BARTSCH, R. A. SYNTHESIS OF CHEMICALLY MODIFIED CYCLODEXTRINS. 1983, 39,1417. TETRAHEDRONa
  158852. GABRIEL WEATHERHEAD
  158853. 8783N
  158854. 2/28/96V
  158855. A REVIEW.  PARRY, R. J. BIOSYNTHESIS OF SOME SULFUR CONTAINING NATURAL PRODUCTS. INVESTIGATIONS OF THE MECHNNISM OF CARBON SULFUR BOND FORMATION. 1983, 39,1215. TETRAHEDRONa
  158856. GABRIEL WEATHERHEAD
  158857. 8784N
  158858. 2/28/96VdA REVIEW.  MENGER, F. M. DIRECTIONALITY OF ORGANIC REACTIONS IN SOLUTION. 1983, 39,1013. TETRAHEDRONa
  158859. GABRIEL WEATHERHEAD
  158860. 8785N
  158861. 2/28/96V`A REVIEW. GASC, M. B.; LATTES, A.; PERIE, J. J. AMINATION OF ALKENES. 1983, 39, 703. TETRAHEDRONa
  158862. GABRIEL WEATHERHEAD
  158863. 8786N
  158864. 2/28/96VjA REVIEW. SALOMON, R. G. HOMOGENEOUS METAL CATALYSIS IN ORGANIC PHOTOCHEMISTRY. 1983, 39, 485. TETRAHEDRON
  158865. GABRIEL WEATHERHEAD
  158866. 8787N
  158867. 2/28/96V
  158868. A REVIEW. KANE, V. V.; SINGH, V.; MARTIN, A., DOYLE, D. L. THE CHEMISTRY OF 1,2 CARBONYL TRANSPOSITION. 1983, 39, 345. TETRAHEDRONa
  158869. GABRIEL WEATHERHEAD
  158870. 8788N
  158871. 2/28/96V
  158872. A REVIEW.  WERSTIUK, N. H. HOMOENOLATE ANIONS NND HOMOENOLATE ANION EQUIVALENTS. MECHANISTIC ASPECTS AND SYNTHETIC APPLICATIONS. 1983, 39, 205. TETRAHEDRONa
  158873. GABRIEL WEATHERHEAD
  158874. 8789N
  158875. 2/28/96V@A REVIEW.  NARANG, S. A. DNA SYNTHESIS. 1983, 39, 3. TETRAHEDRONa
  158876. GABRIEL WEATHERHEAD
  158877. 8790N
  158878. 2/28/96VvA REVIEW. L'ABBE, G. SOME RING TRNNSFORMATION RENATIONS OF SULFUR CONTAINING HETEROCYCLES. 1982, 38, 3537. TETRAHEDRONa
  158879. GABRIEL WEATHERHEAD
  158880. 8791N
  158881. 2/28/96V
  158882. A REVIEW.  HICKMOTT, P. W. ENAMINES: RECENT ADVANCES IN SYNTHETIC, SPECTROSCOPIC, MECHANISTIC, AND STEREOCHEMICAL ASPECTS
  158883. II. 1982, 38, 3363. TETRAHEDRONa
  158884. GABRIEL WEATHERHEAD
  158885. 8792N
  158886. 2/28/96
  158887. VaA REVIEW.  MORTON, T. H. GAS PHASE ANALOGUES OF SOLVOLYSIS REACTIONS. 1982, 38, 3195. TETRAHEDRONa
  158888. GABRIEL WEATHERHEAD
  158889. 8793N
  158890. 2/28/96V
  158891. A REVIEW. WEINREB, S. M.; STAIB, R. R. SYNTHETIC ASPECTS OF DIELS ALDER CYCLOADDITIONS WITH HETERODIENOPHILES. 1982, 38, 3087. TETRAHEDRONa
  158892. GABRIEL WEATHERHEAD
  158893. 8794N
  158894. 2/28/96VZA REVIEW. SANTELLI ROUVIER, C.; SANTELLI, M. THE NAZAROV CYCLIZATION. 1983, 429. SYNTHESISa
  158895. GABRIEL WEATHERHEAD
  158896. 8795N
  158897. 2/28/96VDA REVIEW. BECKER, K. B. SYNTHESIS OF STILBENES. 1983, 341. SYNTHESISa
  158898. GABRIEL WEATHERHEAD
  158899. 8796N
  158900. 2/28/96VPA REVIEW. BHATT, M. V.; KULKARNI, S. U. CLEAVAGE OF ETHERS. 1983, 249. SYNTHESISa
  158901. GABRIEL WEATHERHEAD
  158902. 8797N
  158903. 2/28/96VlA REVIEW. YAKOBSON, G. G., AKHMETOVA, N. E. ALKALI METAL FLUORIDES IN ORGANIC SYNTHESIS. 1983,169. SYNTHESISa
  158904. GABRIEL WEATHERHEAD
  158905. 8798N
  158906. 2/28/96
  158907. VUA REVIEW. BROWNBRIDGE, P. SILYL ENOL ETHERS IN SYNTHESIS
  158908. PART II. 1983, 85. SYNTHESISa
  158909. GABRIEL WEATHERHEAD
  158910. 8799N
  158911. 2/28/96VSA REVIEW.  BROWNBRIDGE, P. SILYL ENOL ETHERS IN SYNTHESIS
  158912. PART I. 1983, 1 SYNTHESISa
  158913. GABRIEL WEATHERHEAD
  158914. 8800N
  158915. 2/28/96V
  158916. A REVIEW.  GOKEL, G. W.; DISHONG, D. M.; SCHULTZ, R. A.; GATTO, V. J. SYNTHESES OF ALIPHATIC AZACROWN COMPOUNDS. 1982, 997. SYNTHESISa
  158917. GABRIEL WEATHERHEAD
  158918. 8801N
  158919. 2/28/96V
  158920. A REVIEW. PORSHNEV, YU. N.; MOCHALIN, V. B.; CHERKASHIN, M. I. POLYCYCLIC AZULENOID SYSTEMS. 1982, 51,1089. RUSSIAN CHEMICAL REVIEWSa
  158921. GABRIEL WEATHERHEAD
  158922. 8802N
  158923. 2/28/96VmA REVIEW.  DENISOVA DYATLOVN, 0. A.; GLYZIN, V. I. NATURAL XANTHONES. 1982, 51,1007. RUSSIAN CHEMICAL REVIEWSa
  158924. GABRIEL WEATHERHEAD
  158925. 8803N
  158926. 2/28/96
  158927. A REVIEW. MILAEVA, E. R.; RUBEZHOV, A. Z.; PROKOF
  158928. EV, A. I.; OKHLOBYSTIN, 0. YU. THE UNPAIRED ELECTRON IN TRANSITION METAL COMPLEXES. 1982, 51, 942. RUSSIAN CHEMICAL REVIEWSa
  158929. GABRIEL WEATHERHEAD
  158930. 8804N
  158931. 2/28/96V
  158932. A REVIEW. NIFANT'EV, E. E.; ZAVALISHINA, A. I. ADVANCES IN THE CHEMISTRY OF PHOSPHORUS(III) 1,3,2 DIHETEROPHOSPHORINANES. 1982, 51, 921. RUSSIAN CHEMICAL REVIEWSa
  158933. GABRIEL WEATHERHEAD
  158934. 8805N
  158935. 2/28/96VZA REVIEW.  GILYAROV, V. A. PHOSPHORUS ACID AZIDES. 1982, 51, 909. RUSSIAN CHEMICAL REVIEWSa
  158936. GABRIEL WEATHERHEAD
  158937. 8806N
  158938. 2/28/96V
  158939. A REVIEW.  VUROV, S. V.; SMIRNOVA, M. P. PROTECTION OF THE AMINO GROUP IN PEPTIDE SYNTHESIS. 1982, 51, 902. RUSSIAN CHEMICAL REVIEWSa
  158940. GABRIEL WEATHERHEAD
  158941. 8807N
  158942. 2/28/96VoA REVIEW. MAVROV, M. V. ADVANCES IN THE CHEMISTRY OF A HALOGENOALLENES. 1982, 51, 887. RUSSIAN CHEMICAL REVIEWSa
  158943. GABRIEL WEATHERHEAD
  158944. 8808N
  158945. 2/28/96
  158946. A REVIEW.  KAMERNITSKII, A. V., TURUTA, A. M. REACTIVITY AND CONFORMATION OF SYSTEMS CONTAINING A THREE MEMBERED HETEROCYCLE CONJUGATED VITH AN UNSATURATED GROUP. 1982 51, 872. RUSSIAN CHEMICAL REVIEWSa
  158947. GABRIEL WEATHERHEAD
  158948. 8809N
  158949. 2/28/96V
  158950. A REVIEW. VORONKOV, M. G.; KNUTOV, V. I. ADVANCES IN THE CHEMISTRY OF SULPHUR CONTAINING MACROHETEROCYCLES. 1982, 51, 856 RUSSIAN CHEMICAL REVIEWSa
  158951. GABRIEL WEATHERHEAD
  158952. 8810N
  158953. 2/28/96V
  158954. A REVIEW. VALTERS, R. THE ELECTRONIC AND STERIC EFFECTS IN HETEROLYTIC INTRAMOLECULAR CYCLIZATION REACTIONS. 1982, 51, 788. RUSSIAN CHEMICAL REVIEWSa
  158955. GABRIEL WEATHERHEAD
  158956. 8811N
  158957. 2/28/96V
  158958. A REVIEW. KOZINA, M. P.; MASTRYUKOV, V. S.; MIL'VITSKAYA, E. M. THE STRAIN ENERGY, GEOMETRICAL STRUCTURE, AND SPIN SPIN COUPLING CONSTANTS OF CYCLIC HYDROCARBONS. 1982, 51, 765. RUSSIAN CHEMICAL REVIEWSa
  158959. GABRIEL WEATHERHEAD
  158960. 8812N
  158961. 2/28/96
  158962. A REVIEW. CHERKASOV, R. A.; OVCHINNIKOV, V. V.; PUDOVIK M. A. ;PUDOVIK A. N. THE REACTIVITY OF 1,3,2 DIHETEROPHOSPHOLANS AND 1,3,2 DIHETEROPHOSPHORINANES WITH A TETRACOORDINATE PHOSPHORUS ATOM. 1982, 51, 746. RUSSIAN CHEMICAL REVIEWSa
  158963. GABRIEL WEATHERHEAD
  158964. 8813N
  158965. 2/28/96V
  158966. A REVIEW. DALOUTIN, V. I.; PASHKEVICH, K. I.; POSTOVSKII, I. YA. FLUORINE CONTAINING A DICARBONYL COMPOUNDS AND THEIR DERIVATIVES. 1982, 51, 736. RUSSIAN CHEMICAL REVIEWSa
  158967. GABRIEL WEATHERHEAD
  158968. 8814N
  158969. 2/28/96V
  158970. A REVIEW.  FOKIN, A. V.; SUDNEV, YU. N.; KUZNETSOVA, L. D.; KROTOVICH, I. N. REACTIONS OF PEROXYDISULPHURYL DIFLUORIDE AND HALOGEN FLUOROSULPHATES WITH ORGANIC COMPOUNDS. 1982 51, 719. RUSSIAN CHEMICAL REVIEWSa
  158971. GABRIEL WEATHERHEAD
  158972. 8815N
  158973. 2/28/96V
  158974. A REVIEW. ZDANOVICH, V. I.; SEITEMBETOVA, A. ZH.; SETKINA, V. N. TRANSITION METAL COMPLEXES OF CYCLOPENTADIENYLIDES AND PENTAFULVENES. 1982, 51, 659. RUSSIAN CHEMICAL REVIEWSa
  158975. GABRIEL WEATHERHEAD
  158976. 8816N
  158977. 2/28/96VvA REVIEW. VLAD, P. F. THE CHEMISTRY OF PERFUMES BASED ON LABDANE DITERPENOIDS. 1982, 51, 644. RUSSIAN CHEMICAL REVIEWSa
  158978. GABRIEL WEATHERHEAD
  158979. 8817N
  158980. 2/28/96V
  158981. A REVIEW.  KLABUNOVSKII, E. I. ADVANCES IN ENANTIOSELECTIVE HYDROGENATION IN THE PRESENCE OF CHIRAL COMPLEXES OF RHODIUM PALLADIUM, AND COBALT. 1982, 51, 630. RUSSIAN CHEMICAL REVIEWSa
  158982. GABRIEL WEATHERHEAD
  158983. 8818N
  158984. 2/28/96VrA REVIEW. BOGATSKII, A. V.; ZHILINA, Z. I. STERICALLY HINDERED PORPHYRINS. 1982, 51, 592. RUSSIAN CHEMICAL REVIEWSa
  158985. GABRIEL WEATHERHEAD
  158986. 8819N
  158987. 2/28/96V
  158988. A REVIEW. FILIPPOVA, T. V.; BLYUMBERG, E. A. MECHANISM OF THE EPOXIDATION OF ALKENES BY MOLECULAR OXYGEN. 1982, 51, 582. RUSSIAN CHEMICAL REVIEWSa
  158989. GABRIEL WEATHERHEAD
  158990. 8820N
  158991. 2/28/96V
  158992. A REVIEW. KASHIN, A. N.; KELETSKAYA, I. P. OXIDATION OF ORGANOMETALLIC COMPOUNDS BY TRANSITION METAL SALTS. 1982, 51 503. RUSSIAN CHEMICAL REVIEWS
  158993. GABRIEL WEATHERHEAD
  158994. 8821N
  158995. 2/28/96V
  158996. A REVIEW.  ZVEZDINA, E. A., ZHADONVA, M. P., DOROFEENKO, G. N. REACTIONS OF PYRYLIUM SALTS WITH NITROGEN CONTAINING NUCLEOPHILES. 1982, 51, 469. RUSSIAN CHEMICAL REVIEWSa
  158997. GABRIEL WEATHERHEAD
  158998. 8822N
  158999. 2/28/96VgA REVIEW. DOMBROVSKII, A. V. HALOGEN DERIVATIVES OF 1,4 DIOXAN. 1982, 51, 457. RUSSIAN CHEMICAL REVIEWSa
  159000. GABRIEL WEATHERHEAD
  159001. 8823N
  159002. 2/28/96VxA REVIEW. STARODUB, V. A., KRIVOSHEI, I. V. HIGHLY ANISOTROPIC MOLECULAR SOLIDS. 1982, 51, 439. RUSSIAN CHEMICAL REVIEWSa
  159003. GABRIEL WEATHERHEAD
  159004. 8824N
  159005. 2/28/96
  159006. A REVIEW. LAARHOVEN, W. H. PHOTOCHEMICAL CYCLIZATIONS AND INTRAMOLECULAR CYCLOADDITIONS OF CONJUGATED ARYLOLEFINS. PART 2: PHOTOCYCLIZATIONS WITHOUT DEHYDROGENATION OF PHOTOCYCLOADDITIONS. 1983, 102, 241. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETY
  159007. GABRIEL WEATHERHEAD
  159008. 8825N
  159009. 2/28/96
  159010. A REVIEW. LAARHOVEN, W. H. PHOTOCHEMICAL CYCLIZATIONS AND INTRAMOLECULAR CYCLOADDITIONS OF CONJUGATED ARYLOLEFINS. 1983, 102, 185. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  159011. GABRIEL WEATHERHEAD
  159012. 8826N
  159013. 2/28/96V
  159014. A REVIEW. ALTONA, C. CONFORMATIONAL ANALYSIS OF NUCLEIC ACIDS. DETERMINATION OF BACKBONE GEOMETRY OF SINGLE HELICAL RNA AND DNA IN AQUEOUS SOLUTION. 1982,101, 413. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  159015. GABRIEL WEATHERHEAD
  159016. 8827N
  159017. 2/28/96V
  159018. A REVIEW. WIERSUM, U. E. FLASH VACUUM THERMOLYSIS, A VERSATILE METHOD IN ORGANIC CHEMISTRY. PART II, FRAGMENTATION PATTERNS IN SPECIFIC CLASSES. 1982, LOL, 365. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  159019. GABRIEL WEATHERHEAD
  159020. 8828N
  159021. 2/28/96V
  159022. A REVIEW.  KOSKINEN, A.; LOUNASMAA, M. THE SARPAGIN AJMALINE GROUP OF INDOLE ALKALOIDS. 1983, 43, 267. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  159023. GABRIEL WEATHERHEAD
  159024. 8829N
  159025. 2/28/96V
  159026. A REVIEW. INGHAM, J. I. NATURALLY OCCURRING ISOFLAVONOIDS (1855 1981). 1983, 43, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  159027. GABRIEL WEATHERHEAD
  159028. 8830N
  159029. 2/28/96V
  159030. A REVIEW. ASAKAWA, Y. CHEMICAL CONSTITUENTS OF THE HEPATICAE. 1982, 42, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  159031. GABRIEL WEATHERHEAD
  159032. 8831N
  159033. 2/28/96VqA REVIEW.  CRANDALL, J. K.; APPARU, M. BASE PROMOTED ISOMERIZATIONS OF EPOXIDES. 1983, 29, 345. ORGANIC REACTIONSa
  159034. GABRIEL WEATHERHEAD
  159035. 8832N
  159036. 2/28/96V
  159037. A REVIEW.  NOYORI, R.; HAYAKAWA, Y. REDUCTIVE DEHALOGENATION OF POLYHALO KETONES WITH LOW VALENT METALS AND RELATED REDUCING AGENTS. 1983, 29, 163. ORGANIC REACTIONSa
  159038. GABRIEL WEATHERHEAD
  159039. 8833N
  159040. 2/28/96V
  159041. A REVIEW. CASTRO, B. R. REPLACEMENT OF ALCOHOLIC HYDROXYL GROUPS BY HALOGENS AND OTHER NUCLEOPHILES VIA OXYPHOSPHONIUM INTERMEDIATES. 1983, 29, 1. ORGANIC REACTIONS
  159042. GABRIEL WEATHERHEAD
  159043. 8834N
  159044. 2/28/96V
  159045. A REVIEW. DE KIMPE, N.; SCHAMP, N. REACTIVITY OF ,B HALOENAMINES. 1983, 15, 71. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  159046. GABRIEL WEATHERHEAD
  159047. 8835N
  159048. 2/28/96V{A REVIEW. WITCZAK, Z. J. SYNTHESIS AND PREPARATIVE APPLICATIONS OF MONOSACCHARIDE THIOCYANATES. 1983, 20,1435. HETEROCYCLESa
  159049. GABRIEL WEATHERHEAD
  159050. 8836N
  159051. 2/28/96V
  159052. A REVIEW. SHIN, C. G. STEREOSELECTIVE SYNTHESIS OF THE GEOMETRIC AND OPTICAL ISOMERS OF UNSATURATED 3 MONO  AND 3,6 DISUBSTITUTED 2,5 PIPERAZINEDIONES. 1983, 20, 1407. HETEROCYCLESa
  159053. GABRIEL WEATHERHEAD
  159054. 8837N
  159055. 2/28/96V
  159056. A REVIEW. COCAGNE, P.; ELGUERO, J.; GALLO, R. THE PRESENT USE AND THE POSSIBILITIES OF PHASE TRANSFER CATALYSIS IN DRUG SYNTHESIS. 1983, 20,1379. HETEROCYCLESa
  159057. GABRIEL WEATHERHEAD
  159058. 8838N
  159059. 2/28/96
  159060. VwA REVIEW.  IDDON, B. CYCLOADDITION, RING OPENING, AND OTHER NOVEL REACTIONS OF THIOPHENES. 1983, 20, 1127. HETEROCYCLESa
  159061. GABRIEL WEATHERHEAD
  159062. 8839N
  159063. 2/28/96V
  159064. A REVIEW. BROADBENT, T. A.; PAUL, E. G. CARBON 13 NUCLEAR MAGNETIC RESONANCE IN ALKALOID CHEMISTRY. 1983, 20, 863. HETEROCYCLESa
  159065. GABRIEL WEATHERHEAD
  159066. 8840N
  159067. 2/28/96
  159068. A REVIEW. BOX, V. G. S. THE ROLE OF LONE PAIR INTERACTIONS IN THE SELECTIVE FUNCTIONALIZATION OF SOME 4,6 0 BENZYLIDENEHEXOPYRANOSIDES BY BOTH THE PHASE TRANSFER ESTERIFICATION REACTIONS AND THE TIN MEDIATED ESTERIFICATION AND ALKYLATION REACTIONS. 1983, 20, 677. HETEROCYCLES
  159069. GABRIEL WEATHERHEAD
  159070. 8841N
  159071. 2/28/96V
  159072. A REVIEW. ELNAGDI, M. H.; ELFAHHAM, H. A.; ELGEMEIE, G. E. H. UTILITY OF A,B UNSATURATED NITRILES IN HETEROCYCLIC SYNTHESIS. 1983, 20, 519. HETEROCYCLESa
  159073. GABRIEL WEATHERHEAD
  159074. 8842N
  159075. 2/28/96
  159076. VqA REVIEW.  SARAF, S.; KHAN, M. A.; AL MOUSAWI, S. INFRARED SPECTRA OF PHENOTHIAZINES. 1983, 20, 283. HETEROCYCLESa
  159077. GABRIEL WEATHERHEAD
  159078. 8843N
  159079. 2/28/96VXA REVIEW. LEE, S. J.; COOK, J. M. SYNTHESIS OF AZAPHENALENES. 1983, 20, 87. HETEROCYCLESa
  159080. GABRIEL WEATHERHEAD
  159081. 8844N
  159082. 2/28/96VgA REVIEW. SLIWA, W.; THOMAS, A. FUSED 1,2,5 THIADIAZOLES AND SELENADIAZOLES. 1983, 20, 71. HETEROCYCLESa
  159083. GABRIEL WEATHERHEAD
  159084. 8845N
  159085. 2/28/96VnA REVIEW. MURPHY, W. 5.; SATTANASIN, S. ANIONIC CYCLIZATION OF PHENOLS. 1983,12, 213. CHEMICAL SOCIETY REVIEWSa
  159086. GABRIEL WEATHERHEAD
  159087. 8846N
  159088. 2/28/96V
  159089. A REVIEW.  SCRIVEN, E. F. V. 4 DIALKYLAMINOPYRIDINES: SUPER ACYLATION AND ALKYLATION CATALYSTS. 1983,12,129. CHEMICAL SOCIETY REVIEWSa
  159090. GABRIEL WEATHERHEAD
  159091. 8847N
  159092. 2/28/96V|A REVIEW. REDPATH, J.; ZEELEN, F. J. STEREOSELECTIVE SYNTHESIS OF STEROID SIDE CHAINS. 1983,12, 75. CHEMICAL SOCIETY REVIEWS
  159093. GABRIEL WEATHERHEAD
  159094. 8848N
  159095. 2/28/96VfA REVIEW. GILCHRIST, T. L. NITROSO ALKENES AND NITROSO ALKYNES. 1983, 12, 53. CHEMICAL SOCIETY REVIEWSa
  159096. GABRIEL WEATHERHEAD
  159097. 8849N
  159098. 2/28/96VgA REVIEW.  AGER, D. J. SILICON CONTAINING CARBONYL EQUIVALENTS. 1982, 11, 493. CHEMICAL SOCIETY REVIEWSa
  159099. GABRIEL WEATHERHEAD
  159100. 8850N
  159101. 2/28/96V^A REVIEW.  MORRIS, D. G. CARBONYL GROUP TRANSPOSITIONG. 1982,11, 397. CHEMICAL SOCIETY REVIEWSa
  159102. GABRIEL WEATHERHEAD
  159103. 8851N
  159104. 2/28/96VzA REVIEW. HOLLAND, H. L. THE MECHANISM OF THE MICROBIAL HYDROXYLATION OF STEROIDS. 1982, 11, 371. CHEMICAL SOCIETY REVIEWSa
  159105. GABRIEL WEATHERHEAD
  159106. 8852N
  159107. 2/28/96V
  159108. A REVIEW. ACKROYD, J.; SCHEINMANN, F. THE SYNTHESIS OF LEUKOTRIENES: A NEW CLASS OF BIOLOGICALLY ACTIVE COMPOUNDS INCLUDING SRS A. 1982,11, 321. CHEMICAL SOCIETY REVIEWSa
  159109. GABRIEL WEATHERHEAD
  159110. 8853N
  159111. 2/28/96
  159112. VlA REVIEW. MUETTERTIES, E. L. HYDROCARBON REACTIONS AT METAL CENTRES. 1982, 11, 283. CHEMICAL SOCIETY REVIEWSa
  159113. GABRIEL WEATHERHEAD
  159114. 8854N
  159115. 2/28/96V
  159116. A REVIEW. SEEMAN, J. I. EFFECT OF CONFORMATIONAL CHANGE ON REACTIVITY IN ORGANIC CHEMISTRY. EVALUATIONS, APPLICATIONS AND EXTENSIONS OF CURTIN HAMMETT/WINSTEIN HOLNESS KINETICS. 1983, 83, 83. CHEMICAL REVIEWSa
  159117. GABRIEL WEATHERHEAD
  159118. 8855N
  159119. 2/28/96V~A REVIEW. DILLING, W. L. POLYMERIZATION OF UNSATURATED COMPOUNDS BY PHOTOCYCLOADDITION REACTIONS. 1983, 83,1. CHEMICAL REVIEWSa
  159120. GABRIEL WEATHERHEAD
  159121. 8856N
  159122. 2/28/96V_A REVIEW. ZEFIROV, N. S.; MAKHON'KOV, D. I. X PHILIC REACTIONS. 1982, 82, 615. CHEMICAL REVIEWSa
  159123. GABRIEL WEATHERHEAD
  159124. 8857N
  159125. 2/28/96V
  159126. A REVIEW.  FABRE, P. L.; DEVYNCK, J.; TREMILLON, B. THERMODYNAMIC BEHAVIOR OF ALKANES IN SUPERACID MEDIA. 1982, 82, 591. CHEMICAL REVIEWSa
  159127. GABRIEL WEATHERHEAD
  159128. 8858N
  159129. 2/28/96
  159130. A REVIEW.  SEEVERS, R. H.; COUNSELL, R. E. RADIOIODINATION TECHNIQUES FOR SMALL ORGANIC MOLECULES. 1982, 82, 575. CHEMICAL REVIEWSa
  159131. GABRIEL WEATHERHEAD
  159132. 8859N
  159133. 2/28/96V
  159134. A REVIEW. HALL, H. K., JR. BOND FORMING INITIATION IN SPONTANEOUS ADDITION AND POLYMERIZATION REACTIONS OF ALKENES. 1983, 22, 440. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159135. GABRIEL WEATHERHEAD
  159136. 8860N
  159137. 2/28/96V
  159138. A REVIEW.  PRAKASH, C. K. S.; RAWDAH, T. N.; OLAH, G. A. STABLE CARBODICATIONS. 1983, 22, 390. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159139. GABRIEL WEATHERHEAD
  159140. 8861N
  159141. 2/28/96V
  159142. A REVIEW.  STELLA, L. HOMOLYTIC CYCLIZATION OF N CHLOROALKENYLAMINES [NEW SYNTHETIC METHODS (38)]. 1983, 22, 337. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159143. GABRIEL WEATHERHEAD
  159144. 8862N
  159145. 2/28/96
  159146. A REVIEW. MARTIN, H. D.; MAYER B. PROXIMITY EFFECTS IN ORGANIC CHEMISTRY
  159147. THE PHOTOELECTRON SPECTROSCOPIC INVESTIGATION OF NON BONDING AND TRANSANNULAR INTERACTIONS. 1983, 22 283. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159148. GABRIEL WEATHERHEAD
  159149. 8863N
  159150. 2/28/96V
  159151. A REVIEW. VAN DE SANDE, C. C. DYE DIFFUSION SYSTEMS IN COLOR PHOTOGRAPHY. 1983, 22,191. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159152. GABRIEL WEATHERHEAD
  159153. 8864N
  159154. 2/28/96V
  159155. A REVIEW.  KAIM, W. THE VERSATILE CHEMISTRY OF 1,4 DIAZINES: ORGANIC, INORGANIC AND BIOCHEMICAL ASPECTS. 1983, 22,171. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159156. GABRIEL WEATHERHEAD
  159157. 8865N
  159158. 2/28/96V
  159159. A REVIEW.  WEIDMANN, B.; SEEBACH, D. ORGANOMETALLIC COMPOUNDS OF TITANIUM AND ZIRCONIUM AS SELECTIVE NUCLEOPHILIC REAGENTS IN ORGANIC SYNTHESIS. 1983, 22, 31. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159160. GABRIEL WEATHERHEAD
  159161. 8866N
  159162. 2/28/96
  159163. A REVIEW.  OSAWA, E.; MUSSO, H. MOLECULAR MECHANICS CALCULATIONS IN ORGANIC CHEMISTRY: EXAMPLES OF THE USEFULNESS OF THIS SIMPLE NON QUANTUM MECHANICAL MODEL. 1983, 22,1. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159164. GABRIEL WEATHERHEAD
  159165. 8867N
  159166. 2/28/96V
  159167. A REVIEW. SAMUELSSON, B. THE LEUKOTRIENES. HIGHLY BIOLOGICALLY ACTIVE SUBSTANCES INVOLVED IN ALLERGY AND INFLAMMATION. 1982, 21, 902. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  159168. GABRIEL WEATHERHEAD
  159169. 8868N
  159170. 2/28/96VrA REVIEW. WHITESIDES, G. M.; WONG, C. H. ENZYMES AS CATALYSTS IN ORGANIC SYNTHESIS. 1983,16, 27. ALDRICHIMICA ACTAa
  159171. GABRIEL WEATHERHEAD
  159172. 8869N
  159173. 2/28/96VfA REVIEW. STANG, P. J.; WHITE, M. R. TRIFLIC ACID AND ITS DERIVATIVES. 1983, 16, 15. ALDRICHIMICA ACTAa
  159174. GABRIEL WEATHERHEAD
  159175. 8870N
  159176. 2/28/96VdA REVIEW.  BLACK, T. H. THE PREPARATION AND REACTIONS OF DIAZOMETHANE. 1983,16, 3. ALDRICHIMICA ACTAa
  159177. GABRIEL WEATHERHEAD
  159178. 8871N
  159179. 2/28/96V
  159180. A REVIEW. MASAMUNE, S.; CHOY, W. ADVANCES IN STEREOCHEMICAL CONTROL: THE 1,2  AND 1,3 DIOL SYSTEMS. 1982, 15 47. ALDRICHIMICA ACTAa
  159181. GABRIEL WEATHERHEAD
  159182. 8872N
  159183. 2/28/96ViA REVIEW. WILLIAMS, D. L. H. NITROSATION MECHANISMS. 1983,19, 381. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  159184. GABRIEL WEATHERHEAD
  159185. 8873N
  159186. 2/28/96V
  159187. A REVIEW.  AHLBERG, P., JONSALL, ENGDAHL, C. DEGENERATE CARBOCATION REARRANGEMENTS. 1983, 19, 223 ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  159188. GABRIEL WEATHERHEAD
  159189. 8874N
  159190. 2/28/96V
  159191. A REVIEW. PARKER, V. D. THE STUDY OF REACTIVE INTERMEDIATES BY ELECTROCHEMICAL METHODS. 1983,19,131. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  159192. GABRIEL WEATHERHEAD
  159193. 8875N
  159194. 2/28/96V
  159195. A REVIEW. DAVIDSON, R. S. THE CHEMISTRY OF EXCITED COMPLEXES: A SURVEY OF REACTIONS. 1983,19,1. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  159196. GABRIEL WEATHERHEAD
  159197. 8876N
  159198. 2/28/96
  159199. 0VkA REVIEW.  SATGE, J. MULTIPLY BONDED GERMANIUM SPECIES. 1983, 21, 241. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  159200. GABRIEL WEATHERHEAD
  159201. 8877N
  159202. 2/28/96V
  159203. A REVIEW. VAN KOTEN, G.; VRIEZE, K. 1,4 DIAZA 1,3 BUTADIENE (A DIIMINE) LIGANDS: THEIR COORDINATION MODES AND THE REACTIVITY OF THEIR METAL COMPLEXES. 1983, 21,152. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  159204. GABRIEL WEATHERHEAD
  159205. 8878N
  159206. 2/28/96V
  159207. A REVIEW.  DARENSBOURG, D. J. MECHANISTIC PATHWAYS FOR LIGAND SUBSTITUTION PROCESSES IN METAL CARBONYLS. 1983, 21,113. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  159208. GABRIEL WEATHERHEAD
  159209. 8879N
  159210. 2/28/96V
  159211. A REVIEW. HOUSECROFT, C. E.; FEHLNER, T. P. METALLOBORANES: THEIR RELATIONSHIPS TO METAL HYDROCARBON COMPLEXES AND CLUSTERS. 1983, 21, 57. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  159212. GABRIEL WEATHERHEAD
  159213. 8880N
  159214. 2/28/96
  159215. A REVIEW. MACOMBER, D. W., HART, W. P., RAUSCH, M. D. FUNCTIONALLY SUBSTITUTED CYCLOPENTADIENYL METAL COMPOUNDS. 1983, 21, 1. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  159216. GABRIEL WEATHERHEAD
  159217. 8881N
  159218. 2/28/96V|A REVIEW. HERMECZ, I.; MESZAROS, Z. CHEMISTRY OF PYRIDO[1,2 A]PYRIMIDINES. 1983, 33, 242. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159219. GABRIEL WEATHERHEAD
  159220. 8882N
  159221. 2/28/96VhA REVIEW. TIMPE, H. J.; EL'TSOV, A. V. PSEUDOAZULENES. 1983, 33, 185. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159222. GABRIEL WEATHERHEAD
  159223. 8883N
  159224. 2/28/96V
  159225. A REVIEW. PAUDLER, W. W., SHEETS, R. M. RECENT DEVELOPMENTS IN NAPHTHYRIDINE CHEMISTRY. 1983, 33,147. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159226. GABRIEL WEATHERHEAD
  159227. 8884N
  159228. 2/28/96V
  159229. A REVIEW. VAN DER PLAS, H. C.; WOZNIAK, M.; VAN DEN HANK, H. J. W. REACTIVITY OF NAPHTHYRIDINES TOWARD NITROGEN NUCLEOPHILES. 1983, 33, 96. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159230. GABRIEL WEATHERHEAD
  159231. 8885N
  159232. 2/28/96V
  159233. A REVIEW. REID, S. T. THE PHOTOCHEMISTRY OF OXYGEN  AND SULFUR CONTAINING HETEROCYCLES. 1983, 33,1. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159234. GABRIEL WEATHERHEAD
  159235. 8886N
  159236. 2/28/96VZA REVIEW. KURZER, F. 1 2,4 THIADIAZOLES. 1982, 32, 286. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159237. GABRIEL WEATHERHEAD
  159238. 8887N
  159239. 2/28/96VsA REVIEW. SAMMES, M. P.; KATRITZKY, A. R. THE 2H  AND 3H PYRROLES. 1982 32, 234. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159240. GABRIEL WEATHERHEAD
  159241. 8888N
  159242. 2/28/96V
  159243. A REVIEW. KLEMM, L. H. SYNTHESES OF TETRACYCLIC AND PENTACYCLIC CONDENSED THIOPHENE SYSTEMS. 1982, 32,127. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159244. GABRIEL WEATHERHEAD
  159245. 8889N
  159246. 2/28/96VvA REVIEW.  BARKER, J. M. GEM DIETHIENYLALKANES AND THEIR DERIVATIVES. 1982, 32, 83. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159247. GABRIEL WEATHERHEAD
  159248. 8890N
  159249. 2/28/96
  159250. >VyA REVIEW. ALBERT, A. ANNELATION OF A PYRIMIDINE RING TO AN EXISTING RING. 1982, 32, 3. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  159251. GABRIEL WEATHERHEAD
  159252. 8891N
  159253. 2/28/96V
  159254. A REVIEW.  ZAMOISKI, A., BANASZEK, A.; GRYNKIEWICZ, G. THE SYNTHESIS OF SUGARS FROM NON CARBOHYDRATE SUBSTRATES. 1982, 40, 1 ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  159255. GABRIEL WEATHERHEAD
  159256. 8892N
  159257. 2/28/96VmA REVIEW. LOWE, G. CHIRAL [L6O,L7O,18O]PHOSPHATE ESTER. 1983,16, 244. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159258. GABRIEL WEATHERHEAD
  159259. 8893N
  159260. 2/28/96V
  159261. A REVIEW. SCHULTZ, A. G. PHOTOCHEMICAL SIX ELECTRON HETEROCYCLIZATION REACTIONS. 1983,16, 210. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159262. GABRIEL WEATHERHEAD
  159263. 8894N
  159264. 2/28/96VgA REVIEW. MILLER, L. L. ORGANIC PLASMA CHEMISTRY. 1983,16, 194. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159265. GABRIEL WEATHERHEAD
  159266. 8895N
  159267. 2/28/96
  159268. A REVIEW. FUKUTO, J. M.; JENSEN, F. R. MECHANISMS OF SE2 REACTIONS: EMPHASIS ON ORGANOTIN COMPOUNDS. 1983,16,177. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159269. GABRIEL WEATHERHEAD
  159270. 8896N
  159271. 2/28/96V~A REVIEW. SERRATOSA, F. ACETYLENE DIETHERS: A LOGAL ENTRY TO OXOCARBONS. 1983,16, 170. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159272. GABRIEL WEATHERHEAD
  159273. 8897N
  159274. 2/28/96V[A REVIEW.  GUTSCHE, C. D. CALIXARENES. 1983,16,161. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159275. GABRIEL WEATHERHEAD
  159276. 8898N
  159277. 2/28/96V
  159278. A REVIEW. ALLEN, F. H., KENNARD, O., TAYLOR, R. SYSTEMATIC ANALYSIS OF STRUCTURAL DATA AS A RESEARCH TECHNIQUE IN ORGANIC CHEMISTRY. 1983,16, 146. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159279. GABRIEL WEATHERHEAD
  159280. 8899N
  159281. 2/28/96V
  159282. A REVIEW. MARIANO, P. S. ELECTRON TRANSFER MECHANISMS IN PHOTOCHEMICAL TRANSFORMATIONS OF IMINIUM SALTS. 1983, 16 140. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159283. GABRIEL WEATHERHEAD
  159284. 8900N
  159285. 2/28/96V
  159286. A REVIEW. GUTHRIE, J. P. THERMODYNAMICS OF METASTABLE INTERMEDIATES IN SOLUTION. 1983, 16,122. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159287. GABRIEL WEATHERHEAD
  159288. 8901N
  159289. 2/28/96VgA REVIEW. KNOWLES, W. S. ASYMMETRIC HYDROGENATION. 1983,16, 106 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159290. GABRIEL WEATHERHEAD
  159291. 8902N
  159292. 2/28/96V
  159293. A REVIEW. OKAMURA, W. H. PERICYCLIC REACTIONS OF VINYLALLENES: FROM CALCIFEROLS TO RETINOIDS AND DRIMANES. 1983, 16, 81. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159294. GABRIEL WEATHERHEAD
  159295. 8903N
  159296. 2/28/96V
  159297. A REVIEW. SWENTON, J. S. QUINONE BIS  AND MONOKETALS VIA ELECTROCHEMICAL OXIDATION. VERSATILE INTERMEDIATES FOR ORGANIC SYNTHESIS. 1983,16, 74. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159298. GABRIEL WEATHERHEAD
  159299. 8904N
  159300. 2/28/96
  159301. A REVIEW. SHANZER, A.; LIBMAN, J.; FROLOW, F. MACROCYCLIC CARBONYL COMPOUNDS AS STRUCTURAL MODELS OF NATURAL ION CARRIERS. 1983, 16, 60. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159302. GABRIEL WEATHERHEAD
  159303. 8905N
  159304. 2/28/96V
  159305. A REVIEW. ADLINGTON, R. M.; BARRETT, A. G. M. RECENT APPLICATIONS OF THE SHAPIRO REACTION. 1983,16, 55. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159306. GABRIEL WEATHERHEAD
  159307. 8906N
  159308. 2/28/96V
  159309. A REVIEW.  MANDER, L. N. NEW STRATEGIES FOR THE CONSTRUCTION OF HIGHLY FUNCTIONALIZED ORGANIC MOLECULES: APPLICATIONS TO CL9 GIBBERELLIN SYNTHESIS. 1983,16, 48. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159310. GABRIEL WEATHERHEAD
  159311. 8907N
  159312. 2/28/96VwA REVIEW. KUCZKOWSKI, R. L. FORMATION AND STRUCTURES OF OZONIDES. 1983, 16, 42. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159313. GABRIEL WEATHERHEAD
  159314. 8908N
  159315. 2/28/96
  159316. A REVIEW. KANAMORI, K.; ROBERTS, J. D. 15N NMR STUDIES OF BIOLOGICAL SYSTEMS. 1983, 16, 35. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159317. GABRIEL WEATHERHEAD
  159318. 8909N
  159319. 2/28/96V
  159320. A REVIEW. MINISCI, F.; CITTERIO, A.; GIORDANO, C. ELECTRON TRANSFER PROCESSES: PEROXYDISULFATE, A USEFUL AND VERSATILE REAGENT IN ORGANIC CHEMISTRY. 1983,16, 27. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159321. GABRIEL WEATHERHEAD
  159322. 8910N
  159323. 2/28/96V
  159324. A REVIEW. HUTCHINSON, C. R. BIOSYNTHETIC STUDIES OF MACROLIDE AND POLYETHER ANTIBIOTICS. 1983,16, 7. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159325. GABRIEL WEATHERHEAD
  159326. 8911N
  159327. 2/28/96V
  159328. A REVIEW. WILLIAMS, F.; SPRAGUE, E. D. NOVEL RADICAL ANIONS AND HYDROGEN ATOM TUNNELING IN THE SOLID STATE. 1982,15, 408. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159329. GABRIEL WEATHERHEAD
  159330. 8912N
  159331. 2/28/96
  159332. A REVIEW.  KWART, H. TEMPERATURE DEPENDENCE OF THE PRIMARY KINETIC HYDROGEN ISOTOPE EFFECT AS A MECHANISTIC CRITERION. 1982, 15, 401. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159333. GABRIEL WEATHERHEAD
  159334. 8913N
  159335. 2/28/96V
  159336. A REVIEW. HAYASHI, T., KUMADA, M. ASYMMETRIC SYNTHESIS CATALYZED BY TRANSITION METAL COMPLEXES WITH FUNCTIONALIZED CHIRAL FERROCENYLPHOSPHINE LIGANDS. 1982, 15, 395. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159337. GABRIEL WEATHERHEAD
  159338. 8914N
  159339. 2/28/96V
  159340. A REVIEW. JARVIS, B. B.; MAZZOLA, E. P. MACROCYCLIC AND OTHER NOVEL TRICHOTHECENES: THEIR STRUCTURE, SYNTHESIS, AND BIOLOGICAL SIGNIFICANCE. 1982,15, 388. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159341. GABRIEL WEATHERHEAD
  159342. 8915N
  159343. 2/28/96V
  159344. A REVIEW. LOWN, J. W. NEWER APPROACHES TO THE STUDY OF THE MECHANISMS OF ACTION OF ANTITUMOR ANTIBIOTICS. 1982,15, 381. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159345. GABRIEL WEATHERHEAD
  159346. 8916N
  159347. 2/28/96
  159348. A REVIEW. YOSHIDA, K. ELECTROOXIDATION IN ORGANIC CHEMISTRY. THE ROLE OF CATION RADICALS AS SYNTHETIC INTERMEDIATES. WILEY INTERSCIENCE: NEW YORK, 1983.a
  159349. GABRIEL WEATHERHEAD
  159350. 8917N
  159351. 2/28/96V
  159352. A REVIEW. WATSON, W. H., ED. STEREOCHEMISTRY AND REACTIVITY OF SYSTEMS CONTAINING P ELECTRONS. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1983.a
  159353. GABRIEL WEATHERHEAD
  159354. 8918N
  159355. 2/28/96VxA REVIEW. VERNIN, G., ED. CHEMISTRY OF HETEROCYCLIC COMPOUNDS IN FLAVORS AND AROMAS. WILEY INTERSCIENCE: NEW YORK, 1983.a
  159356. GABRIEL WEATHERHEAD
  159357. 8919N
  159358. 2/28/96V_A REVIEW. TURNER, W. B., ALDRIDGE, D. C. FUNGAL METABOLITES II. ACADEMIC PRESS: NEW YORK, 1983.a
  159359. GABRIEL WEATHERHEAD
  159360. 8920N
  159361. 2/28/96VhA REVIEW. SCHEFFOLD, R., ED. TRANSITION METALS IN ORGANIC SYNTHESIS. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159362. GABRIEL WEATHERHEAD
  159363. 8921N
  159364. 2/28/96
  159365. ]VqA REVIEW. SAXTON, J. E., ED. INDOLES: MONOTERPENOID INDOLE ALKALOIDS, PART 4. WILEY INTERSCIENCE: NEW YORK, 1983.a
  159366. GABRIEL WEATHERHEAD
  159367. 8922N
  159368. 2/28/96V
  159369. A REVIEW. PORTER, J. W.; SPURGEON, S. L., EDS. BIOSYNTHESIS OF ISOPRENOID COMPOUNDS, VOLUME 2. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159370. GABRIEL WEATHERHEAD
  159371. 8923N
  159372. 2/28/96V
  159373. A REVIEW. PIZEY, J. S., ED. SYNTHETIC REAGENTS, VOLUME 5, THALLIUM(III) ACETATE AND TRIFLUOROACETATE; AMMONIA; IODINE MONOCHLORIDE. WILEY INTERSCIENCE: NEW YORK, 1983.a
  159374. GABRIEL WEATHERHEAD
  159375. 8924N
  159376. 2/28/96VdA REVIEW. NES, W. D. FULLER, G., TSAI, L. S. ISOPENTENOIDS IN PLANTS. MARCEL DEKKER: NEW YORK, 1984.a
  159377. GABRIEL WEATHERHEAD
  159378. 8925N
  159379. 2/28/96VIA REVIEW.  IVIN, K. J. OLEFIN METATHESIS. ACADEMIC PRESS: NEW YORK, 1983.a
  159380. GABRIEL WEATHERHEAD
  159381. 8926N
  159382. 2/28/96VcA REVIEW. HANESSIAN, S. SYNTHETIC DESIGN WITH CHIRAL TEMPLATES. PERGAMON PRESS: ELMSFORD, NY, 1983.
  159383. GABRIEL WEATHERHEAD
  159384. 8927N
  159385. 2/28/96V`A REVIEW.  FUHRHOP, J.; PENZLIN, G. ORGANIC SYNTHESIS. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1983.a
  159386. GABRIEL WEATHERHEAD
  159387. 8928N
  159388. 2/28/96VjA REVIEW.  DICKSON, R. S. ORGANOMETALLIC CHEMISTRY OF RHODIUM AND IRIDIUM. ACADEMIC PRESS: NEW YORK, 1983.a
  159389. GABRIEL WEATHERHEAD
  159390. 8929N
  159391. 2/28/96VnA REVIEW. DESLONGCHAMPS, P. STEREOELECTRONIC EFFECTS IN ORGANIC CHEMISTRY. PERGAMON PRESS: ELMSFORD, NY, 1983.a
  159392. GABRIEL WEATHERHEAD
  159393. 8930N
  159394. 2/28/96VYA REVIEW. BUCHEL, K. H., ED. CHEMISTRY OF PESTICIDES. WILEY INTERSCIENCE: NEW YORK, 1983.a
  159395. GABRIEL WEATHERHEAD
  159396. 8931N
  159397. 2/28/96VSA REVIEW. BROSSI, A., ED. THE ALKALOIDS, VOLUME 21. ACADEMIC PRESS: NEW YORK, 1983.a
  159398. GABRIEL WEATHERHEAD
  159399. 8932N
  159400. 2/28/96VXA REVIEW. BENSON, F. R. THE HIGH NITROGEN COMPOUNDS. WILEY LNTERSCIENCE: NEW YORK, 1983.a
  159401. GABRIEL WEATHERHEAD
  159402. 2/28/96VYA REVIEW. BATES, R. B.; OGLE, C. A. CARBANION CHEMISTRY. SPRINGER VERLAG: NEW YORK, 1983.a
  159403. GABRIEL WEATHERHEAD
  159404. 8934N
  159405. 2/28/96VbA REVIEW. BAIZER, M. M.; LUND, H. ORGANIC ELECTROCHEMISTRY, 2ND ED. MARCEL DEKKER: NEW YORK, 1983.a
  159406. GABRIEL WEATHERHEAD
  159407. 8935N
  159408. 2/28/96V
  159409. A REVIEW.  APSIMON, J., ED. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOLUME 5, SESQUITERPENES. WILEY LNTERSCIENCE: NEW YORK, 1983.a
  159410. GABRIEL WEATHERHEAD
  159411. 8936N
  159412. 2/28/96V
  159413. A REVIEW. MORRIS, D. G. RECENT ADVANCES IN THE CHEMISTRY OF YLIDES. SURVEY OF PROGRESS IN CHEMISTRY, VOLUME 10, G. A. WUBBLES, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159414. GABRIEL WEATHERHEAD
  159415. 8937N
  159416. 2/28/96V
  159417. A REVIEW. SHIMIZU, Y.; KAMIYA, H. BIOACTIVE MARINE BIOPOLYMERS. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159418. GABRIEL WEATHERHEAD
  159419. 8938N
  159420. 2/28/96
  159421. A REVIEW. BURNELL, D. J.; APSIMON, J. W. ECHINODERM SAPONINS. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159422. GABRIEL WEATHERHEAD
  159423. 8939N
  159424. 2/28/96V
  159425. A REVIEW. CHRISTOPHERSON, C. MARINE INDOLES. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159426. GABRIEL WEATHERHEAD
  159427. 8940N
  159428. 2/28/96V
  159429. A REVIEW. ERICKSON, K. L. CONSTITUENTS OF LAURENCIA. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159430. GABRIEL WEATHERHEAD
  159431. 8941N
  159432. 2/28/96V
  159433. A REVIEW. WITHERS, N. DINOFLAGELLATE STEROLS. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159434. GABRIEL WEATHERHEAD
  159435. 8942N
  159436. 2/28/96V
  159437. A REVIEW. BARROW, K. D. BIOSYNTHESIS OF MARINE METABOLITES. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159438. GABRIEL WEATHERHEAD
  159439. 2/28/96V
  159440. A REVIEW.  BERGQUIST, R. P. WELLS, R. J. CHEMOTAXONOMY OF THE PORIFERA: THE DEVELOPMENT OF CURRENT STATUS OF THE FIELD. MARINE NATURAL PRODUCTS, VOLUME 5, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159441. GABRIEL WEATHERHEAD
  159442. 8944N
  159443. 2/28/96V
  159444. A REVIEW. SUTHERLAND, I. CYCLOPHANES AS SYNTHETIC ANALOGUES OF ENZYMES AND RECEPTORS. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159445. GABRIEL WEATHERHEAD
  159446. 8945N
  159447. 2/28/96V
  159448. A REVIEW. ODASHIMA, K.; KOGA, K. CYCLOPHANES IN HOST GUEST CHEMISTRY. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159449. GABRIEL WEATHERHEAD
  159450. 8946N
  159451. 2/28/96VnA REVIEW.  MISUMI, S. MULTILAYERED CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159452. GABRIEL WEATHERHEAD
  159453. 8947N
  159454. 2/28/96VkA REVIEW. HOPF, H. MULTIBRIDGED CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159455. GABRIEL WEATHERHEAD
  159456. 8948N
  159457. 2/28/96V
  159458. A REVIEW. ITO, S.; FUJISE, Y.; FUKAZAWA, Y. NON BENZENOID PHANES.  CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159459. GABRIEL WEATHERHEAD
  159460. 8949N
  159461. 2/28/96VgA REVIEW. PAUDLER, W. HETEROCYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159462. GABRIEL WEATHERHEAD
  159463. 8950N
  159464. 2/28/96VwA REVIEW. ROSENFELD, S. M.; CHOE, K. A. [N] CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159465. GABRIEL WEATHERHEAD
  159466. 8951N
  159467. 2/28/96V
  159468. A REVIEW.  MITCHELL, R. H. NUCLEAR MAGNETIC RESONANCE PROPERTIES AND CONFORMATIONAL BEHAVIOR OF CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159469. GABRIEL WEATHERHEAD
  159470. 8952N
  159471. 2/28/96VtA REVIEW. KEEHN, P. CRYSTAL STRUCTURE OF CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159472. GABRIEL WEATHERHEAD
  159473. 8953N
  159474. 2/28/96
  159475. A REVIEW. LIEBMAN, J. F. THE CONCEPTUAL CHEMISTRY OF CYCLOPHANES. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159476. GABRIEL WEATHERHEAD
  159477. 8954N
  159478. 2/28/96VtA REVIEW. CRAM, D. J. CYCLOPHANES
  159479. A PERSONAL ACCOUNT. CYCLOPHANES, P. M. KEEHN, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159480. GABRIEL WEATHERHEAD
  159481. 8955N
  159482. 2/28/96V
  159483. A REVIEW.  HEINE, H. DIAZIRIDINES, DIAZIRINES, DIAZIRIDINONES, DIAZIRIDINIMINES. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 2, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159484. GABRIEL WEATHERHEAD
  159485. 8956N
  159486. 2/28/96V
  159487. A REVIEW. RICHTER, R.; ULRICH, H. FOUR MEMBERED RINGS WITH TWO N ATOMS. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 2, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983. DIAZETIDINESa
  159488. GABRIEL WEATHERHEAD
  159489. 8957N
  159490. 2/28/96
  159491. A REVIEW. KOPPEL, G. A. SYNTHESIS OF THE BETA LACTAM FUNCTION. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 2, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159492. GABRIEL WEATHERHEAD
  159493. 8958N
  159494. 2/28/96V
  159495. A REVIEW.  MOORE, J. A.; AYERS, R. S. AZETIDINES. CHEMISTRY OF HETEROCYCLIC COMPOUNDS. SMALL RING HETEROCYCLES PART 2, A. HASSNER, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  159496. GABRIEL WEATHERHEAD
  159497. 8959N
  159498. 2/28/96
  159499. BA REVIEW. SPATOLA, A. F. PEPTIDE BACKBONE MODIFICATIONS: A STRUCTURE ACTIVITY ANALYSIS OF PEPTIDES CONTAMING AMIDE BOND SURROGATES, CONFORMATIONAL CONSTRAINTS, AND RELATED BACKBONE REPLACEMENTS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOLUMES 7, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1983.
  159500. GABRIEL WEATHERHEAD
  159501. 8960N
  159502. 2/28/96
  159503. A REVIEW.  ROESKE, R. W.; KENNEDY, S. J. ION TRANSPORTING PEPTIDES. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOLUMES 7, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1983.a
  159504. GABRIEL WEATHERHEAD
  159505. 8961N
  159506. 2/28/96V
  159507. A REVIEW. TEMPE, J. CHEMISTRY AND BIOCHEMISTRY OF OPEN CHAIN IMINO ACIDS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOLUMES 7, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1983.a
  159508. GABRIEL WEATHERHEAD
  159509. 8962N
  159510. 2/28/96
  159511. A REVIEW.  ROCCHI, R.; GLORMANI, V. GLYCOPROTEINS: COVALENT ATTACHMENT OF CARBOHYDRATES OR CARBOHYDRATE DERIVATIVES TO AMINO ACIDS, PEPTIDES, AND PROTEINS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOLUMES 7, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1983.
  159512. GABRIEL WEATHERHEAD
  159513. 8963N
  159514. 2/28/96
  159515. A REVIEW. OLSEN, R. K. THE QUINOXALINE DEPSIPEPTIDE ANTIBIOTICS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOLUMES 7, B. WEINSTEIN, ED., MARCEL DEKKER: NEW YORK, 1983.a
  159516. GABRIEL WEATHERHEAD
  159517. 8964N
  159518. 2/28/96V
  159519. A REVIEW. FLOSS, H. G., TSAI, M. D. STEREOCHEMISTRY OF BIOLOGICAL REACTIONS AT PROPROCHIRAL CENTERS. 1984,15. TOPICS IN STEREOCHEMISTRYa
  159520. GABRIEL WEATHERHEAD
  159521. 8965N
  159522. 2/28/96V
  159523. A REVIEW. NAKAZAKI, M. THE SYNTHESIS AND STEREOCHEMISTRY OF CHIRAL ORGANIC MOLECULES WITH HIGH SYMMETRY. 1984,15. TOPICS IN STEREOCHEMISTRYa
  159524. GABRIEL WEATHERHEAD
  159525. 8966N
  159526. 2/28/96VxA REVIEW.  CURRIU, R. J. P.; GUERIN, C.; MOREAU, J. J. E. STEREOCHEMISTRY AT SILICON. 1984,15. TOPICS IN STEREOCHEMISTRYa
  159527. GABRIEL WEATHERHEAD
  159528. 8967N
  159529. 2/28/96VdA REVIEW. KLARNER, F. G. WALK REARRANGEMENTS IN (N.1.0) SYSTEMS. 1984, 15. TOPICS IN STEREOCHEMISTRYa
  159530. GABRIEL WEATHERHEAD
  159531. 8968N
  159532. 2/28/96
  159533. VwA REVIEW. MURAKAMI, Y. FUNCTIONALIZED CYCLOPHANES AS CATALYSTS AND ENZYME MODELS. 1983,115. TOPICS IN CURRENT CHEMISTRYa
  159534. GABRIEL WEATHERHEAD
  159535. 8969N
  159536. 2/28/96V{A REVIEW. GERSON, F. RADICAL IONS OF PHANES AS STUDIED BY ESR AND ENDOR SPECTROSCOPY. 1983,115. TOPICS IN CURRENT CHEMISTRYa
  159537. GABRIEL WEATHERHEAD
  159538. 8970N
  159539. 2/28/96V
  159540. A REVIEW. HEILBRONNER, E.; YANG, Z. THE ELECTRONIC STRUCTURE OF CYCLOPHANES AS SUGGESTED BY THEIR PHOTOELECTRON SPECTRA. 1983, 115. TOPICS IN CURRENT CHEMISTRYa
  159541. GABRIEL WEATHERHEAD
  159542. 8971N
  159543. 2/28/96V{A REVIEW. TABUSHI, I.; YAMAMURA, K. WATER SOLUBLE CYCLOPHANES AS HOSTS AND CATALYSTS. 1983,113. TOPICS IN CURRENT CHEMISTRYa
  159544. GABRIEL WEATHERHEAD
  159545. 8972N
  159546. 2/28/96VrA REVIEW. BOEKELHEIDE, V. SYNTHESES AND PROPERTIES OF THE [2N] CYCLOPHANES. 1983, 113. TOPICS IN CURRENT CHEMISTRYa
  159547. GABRIEL WEATHERHEAD
  159548. 8973N
  159549. 2/28/96
  159550. A REVIEW. ROSSA, L.; VOGTLE, F. SYNTHESIS OF MEDIO  AND MACROCYCLIC COMPOUNDS BY HIGH DILUTION PRINCIPLE TECHNIQUES. 1983, 113. TOPICS IN CURRENT CHEMISTRYa
  159551. GABRIEL WEATHERHEAD
  159552. 8974N
  159553. 2/28/96VyA REVIEW. KAS, J.; RAUCH, P. LABELED PROTEINS, THEIR PREPARATION AND APPLICATIONS. 1983, 112. TOPICS IN CURRENT CHEMISTRYa
  159554. GABRIEL WEATHERHEAD
  159555. 8975N
  159556. 2/28/96VYA REVIEW. KOSOWER, E. M. STABLE PYRIDINYL RADICALS. 1983,112. TOPICS IN CURRENT CHEMISTRYa
  159557. GABRIEL WEATHERHEAD
  159558. 8976N
  159559. 2/28/96VrA REVIEW. SUZUKI, A. SOME ASPECTS OF ORGANIC SYNTHESIS USING ORGANOBORATES. 1983, 112. TOPICS IN CURRENT CHEMISTRYa
  159560. GABRIEL WEATHERHEAD
  159561. 8977N
  159562. 2/28/96V|A REVIEW.  SZELE, I.; ZOLLINGER, H. AZO COUPLING REACTIONS
  159563.  STRUCTURES AND MECHANISMS. 1983,112. TOPICS IN CURRENT CHEMISTRYa
  159564. GABRIEL WEATHERHEAD
  159565. 8978N
  159566. 2/28/96
  159567. VxA REVIEW. ASTRUC, D. ORGANO IRON COMPLEXES OF AROMATIC COMPOUNDS. APPLICATIONS IN SYNTHESIS. 1983, 39, 4027. TETRAHEDRONa
  159568. GABRIEL WEATHERHEAD
  159569. 8979N
  159570. 2/28/96V|A REVIEW. MARIANO, P. S. THE PHOTOCHEMISTRY OF IMINIUM SALTS AND RELATED HETEROAROMATIC SYSTEMS. 1983, 39, 3845. TETRAHEDRONa
  159571. GABRIEL WEATHERHEAD
  159572. 8980N
  159573. 2/28/96V
  159574. A REVIEW. ALBRIGHT, J. D. REACTIONS OF ACYL ANION EQUIVALENTS DERIVED FROM CYANOHYDRINS, PROTECTED CYANOHYDRINS AND X DIALKYLAMINONITRILES. 1983, 39, 3207. TETRAHEDRONa
  159575. GABRIEL WEATHERHEAD
  159576. 8981N
  159577. 2/28/96V
  159578. A REVIEW. IACOBUCCI, G. A., SWEENY, J. G. THE CHEMISTRY OF ANTHOCYANINS, ANTHOCYANIDINS AND RELATED FLAVYLIUM SALTS. 1983, 39, 3005. TETRAHEDRONa
  159579. GABRIEL WEATHERHEAD
  159580. 8982N
  159581. 2/28/96VVA REVIEW. BOGER, D. L. DIELS ALDER REACTIONS OF AZADIENES. 1983, 39, 2869. TETRAHEDRONa
  159582. GABRIEL WEATHERHEAD
  159583. 8983N
  159584. 2/28/96
  159585. A REVIEW. KLEIN, J. DIRECTIVE EFFECTS IN ALLYLIC AND BENZYLIC POLYMETALATIONS: THE QUESTION OF U STABILIZATION, Y AROMATICITY AND CROSS CONJUGATION. 1983, 39, 2733. TETRAHEDRONa
  159586. GABRIEL WEATHERHEAD
  159587. 8984N
  159588. 2/28/96VkA REVIEW. HARTWIG, W. MODERN METHODS FOR THE RADICAL DEOXYGENATION OF ALCOHOLS. 1983, 39, 2609. TETRAHEDRONa
  159589. GABRIEL WEATHERHEAD
  159590. 8985N
  159591. 2/28/96VbA REVIEW. RASTOGI, R.; SHARMA, S. 2 AMINOBENZIMIDAZOLES IN ORGANIC SYNTHESES. 1983, 861. SYNTHESISa
  159592. GABRIEL WEATHERHEAD
  159593. 8986N
  159594. 2/28/96V
  159595. A REVIEW.  CHUKOVSKAYA, E. C.; FREIDLINA, R. KH.; KUZ'MINA, N. A. REDUCTION OF TRICHLOROMETHYL COMPOUNDS BY HYDROGEN DONORS INDUCED BY TRANSITION METAL CARBONYLS, THEIR COMPLEXES, OR THEIR SALTS. 1983, 773. SYNTHESISa
  159596. GABRIEL WEATHERHEAD
  159597. 8987N
  159598. 2/28/96V
  159599. A REVIEW. CHEIKH, R. B.; CHAABOUNI, R.; LAURENT, A.; MISON, P.; NAFTI, A. SYNTHESIS OF PRIMARY ALLYLIC AMINES. 1983, 685. SYNTHESISa
  159600. GABRIEL WEATHERHEAD
  159601. 8988N
  159602. 2/28/96V
  159603. A REVIEW. RAMADAS, S. R.; SRINIVASAN, P. S.; RAMACHANDRAN, J.; SASTRY, V. V. S. K. METHODS OF SYNTHESIS OF DITHIOCARBOXYLIC ACIDS AND ESTERS. 1983, 605. SYNTHESISa
  159604. GABRIEL WEATHERHEAD
  159605. 8989N
  159606. 2/28/96V
  159607. A REVIEW.  WHITESELL, J. K.; WHITESELL, M. A. ALKYLATION OF KETONES AND ALDEHYDES VIA THEIR NITROGEN DERIVATIVES. 1983, 517. SYNTHESISa
  159608. GABRIEL WEATHERHEAD
  159609. 8990N
  159610. 2/28/96VwA REVIEW. KORSHAK, V. V.; RUSANOV, A. L. PHENYL SUBSTITUTED POLYHETEROARYLENES. 1983, 52, 459. RUSSIAN CHEMICAL REVIEWSa
  159611. GABRIEL WEATHERHEAD
  159612. 8991N
  159613. 2/28/96V
  159614. A REVIEW.  GOLOLOBOV, YU. G.; GUSAR', N. I.; TARASEVICH, A. S. THREE MEMBERED ORGANOPHOSPHORUS HETEROCYCLES. 1983, 52, 446. RUSSIAN CHEMICAL REVIEWSa
  159615. GABRIEL WEATHERHEAD
  159616. 8992N
  159617. 2/28/96
  159618. A REVIEW.  GODOVIKOVA, T. I., RAKITIN, O. A.; KHMEL'NITSKII, L. I. DIAZOTIZATION OF WEAKLY BASIC AROMATIC AND HETEROCYCLIC AMINES IN STRONGLY ACID MEDIA. 1983, 52, 440. RUSSIAN CHEMICAL REVIEWSa
  159619. GABRIEL WEATHERHEAD
  159620. 8993N
  159621. 2/28/96VoA REVIEW. KOLESOV, V. P., PAPINA, T. S. THERMOCHEMISTRY OF HALOETHANES. 1983, 52, 425. RUSSIAN CHEMICAL REVIEWSa
  159622. GABRIEL WEATHERHEAD
  159623. 8994N
  159624. 2/28/96
  159625. A REVIEW. MARINA, N. G.; MONAKOV, YU. B.; RAFIKOV, S. R., PONOMARENKO, V. I. RELATION BETWEEN THE NATURE OF THE COMPONENTS OF TITANIUM CONTAINING ZIEGLER SYSTEMS AND THEIR ACTIVITY AND STEREOSPECIFICITY IN THE POLYMERIZATION OF DIENES. 1983, 52, 413. RUSSIAN CHEMICAL REVIEWS
  159626. GABRIEL WEATHERHEAD
  159627. 8995N
  159628. 2/28/96VgA REVIEW.  GRANIK, V. G. ADVANCES IN THE CHEMISTRY OF AMIDINES. 1983, 52, 377. RUSSIAN CHEMICAL REVIEWSa
  159629. GABRIEL WEATHERHEAD
  159630. 8996N
  159631. 2/28/96
  159632. A REVIEW.  PUDOVIK, M. A.; OVCHINNIKOV, V. V.; CHERKASOV, R. A.; PUDOVIK, A. N. THE REACTIVITY OF 1,3,2 DIHETEROPHOSPHOLANS CONTAINING A TRICOORDINATE PHOSPHORUS ATOM. 1983, 52, 361. RUSSIAN CHEMICAL REVIEWSa
  159633. GABRIEL WEATHERHEAD
  159634. 8997N
  159635. 2/28/96V
  159636. A REVIEW. RAKHMANKULOV, D. L.; ZORIN, V. V.; LATYPOVA, F. N.; ZLOMSKII, S. S.; KARAKHANOV, R. A. THE SYNTHESIS AND REACTIONS OF 1,3 0XATHIACYCLOALKANES. 1983, 52, 360. RUSSIAN CHEMICAL REVIEWSa
  159637. GABRIEL WEATHERHEAD
  159638. 8998N
  159639. 2/28/96V
  159640. A REVIEW. GUK, YU. V.; HYUSHIN, M. A.; GOLOD, E. L.; GIDASPOV, B. V. NITRONIUM SALTS IN ORGANIC CHEMISTRY. 1983, 52, 284. RUSSIAN CHEMICAL REVIEWSa
  159641. GABRIEL WEATHERHEAD
  159642. 8999N
  159643. 2/28/96V
  159644. A REVIEW. SERGEEV, G. B.; SMIRNOV, V. V., ROSTOVSHCHIKOVA, T. N. HYDROCHLORINATION OF UNSATURATED COMPOUNDS. 1983, 52, 259. RUSSIAN CHEMICAL REVIEWSa
  159645. GABRIEL WEATHERHEAD
  159646. 9000N
  159647. 2/28/96
  159648. A REVIEW. KOZHEVNIKOV, I. V. THE MECHANISM OF THE OXIDATIVE COUPLING OF UNSATURATED HYDROCARBONS UNDER THE INFLUENCE OF PALLADIUM(II). 1983, 52,138. RUSSIAN CHEMICAL REVIEWSa
  159649. GABRIEL WEATHERHEAD
  159650. 9001N
  159651. 2/28/96V
  159652. A REVIEW.  MIRONOV, V. A.; FEDEROVICH, A. D.; AKHREM, A. A. SYNTHETIC METHODS FOR CYCLOHEXA 1,3 DIENES. 1983, 61, 43. RUSSIAN CHEMICAL REVIEWSa
  159653. GABRIEL WEATHERHEAD
  159654. 9002N
  159655. 2/28/96V
  159656. A REVIEW. BLOXSIDGE, J. P.; ELVIDGE, J. A. PRACTICAL ASPECTS OF TRITIUM MAGNETIC RESONANCE. 1983,16, 99. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  159657. GABRIEL WEATHERHEAD
  159658. 9003N
  159659. 2/28/96V
  159660. A REVIEW. GORENSTEIN, D. G. NON BIOLOGICAL ASPECTS OF PHOSPHORUS 31 NMR SPECTROSCOPY. 1983,16,1. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  159661. GABRIEL WEATHERHEAD
  159662. 9004N
  159663. 2/28/96
  159664. A REVIEW. SANDERS, J. K. M.; MERSH, J. D. NUCLEAR MAGNETIC DOUBLE RESONANCE; THE USE OF DIFFERENCE SPECTROSCOPY. 1982,15, 353. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  159665. GABRIEL WEATHERHEAD
  159666. 9005N
  159667. 2/28/96V
  159668. A REVIEW.  RINALDI, P. L. THE DETERMINATION OF ABSOLUTE CONFIGURATION USING NUCLEAR MAGNETIC RESONANCE TECHNIQUES. 1982, 15, 291. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  159669. GABRIEL WEATHERHEAD
  159670. 9006N
  159671. 2/28/96V
  159672. A REVIEW. GRAY, N. A. B. COMPUTER ASSISTED ANALYSIS OF CARBON 13 NMR SPECTRAL DATA. 1982,15, 201. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  159673. GABRIEL WEATHERHEAD
  159674. 9007N
  159675. 2/28/96VcA REVIEW. BLOCK, E. OLEFIN SYNTHESIS BY DEOXYGENATION OF VICINAL DIOLS. 1984, 30. ORGANIC REACTIONSa
  159676. GABRIEL WEATHERHEAD
  159677. 9008N
  159678. 2/28/96VyA REVIEW. MALLORY, F. B.; MALLORY, C. W. PHOTOCYCLIZATION OF STILBENES AND RELATED MOLECULES. 1984, 30. ORGANIC REACTIONSa
  159679. GABRIEL WEATHERHEAD
  159680. 9009N
  159681. 2/28/96VmA REVIEW. SHAWALI, A. S. REACTIONS OF HYDRAZIDOYL HALIDES WITH SULFUR COMPOUNDS. 1983, 20, 2239. HETEROCYCLESa
  159682. GABRIEL WEATHERHEAD
  159683. 9010N
  159684. 2/28/96VLA REVIEW. WITKOP, B. FORTY YEARS OF TRYPTO FUN. 1983, 20, 2059. HETEROCYCLESa
  159685. GABRIEL WEATHERHEAD
  159686. 9011N
  159687. 2/28/96V
  159688. A REVIEW. WONG, H. N. C.; NG, T. K.; WONG, T. Y. ARENE SYNTHESES BY EXTRUSION OF HETEROATOMS FROM 7 HETEROATOM BICYCLO[2.2.1]HEPTENE SYSTEMS. 1983, 20,1815. HETEROCYCLESa
  159689. GABRIEL WEATHERHEAD
  159690. 9012N
  159691. 2/28/96V
  159692. A REVIEW. BOX, V. G. S. THE ROLE OF LONE PAIR INTERACTIONS IN THE CHEMISTRY OF MONOSACCHARIDES. THE SELECTIVE ESTERIFICATION OF 4,6 O BENZYLIDENE HEXOPYRANOSIDES. 1983, 20, 1641. HETEROCYCLESa
  159693. GABRIEL WEATHERHEAD
  159694. 9013N
  159695. 2/28/96VzA REVIEW. DABOUN H. A., ABDOU, S. E. RECENT DEVELOPMENTS IN THE CHEMISTRY OF YLIDENE AZOLONES. 1983, 20,1615. HETEROCYCLESa
  159696. GABRIEL WEATHERHEAD
  159697. 9014N
  159698. 2/28/96V
  159699. A REVIEW. TISLER, M. HETEROCYCLIC AMIDINES AND HYDROXYAMIDINES AS SYNTHONS FOR BI  AND POLYCYCLIC HETEROCYCLES. 1983, 20, 1591. HETEROCYCLESa
  159700. GABRIEL WEATHERHEAD
  159701. 9015N
  159702. 2/28/96VyA REVIEW. MAKELA, M. J.; KORPELA, T. K. CHEMICAL MODELS OF ENZYMIC TRANSIMINATION. 1983,12, 309. CHEMICAL SOCIETY REVIEWSa
  159703. GABRIEL WEATHERHEAD
  159704. 9016N
  159705. 2/28/96VoA REVIEW. GUPTA, S. P., SINGH, P.; BINDAL, M. C. QSAR STUDIES ON HALLUCINOGENS. 1983, 83, 633. CHEMICAL REVIEWSa
  159706. GABRIEL WEATHERHEAD
  159707. 9017N
  159708. 2/28/96VPA REVIEW. SALAUN, J. CYCLOPROPANONE HEMIACETALS. 1983, 83, 619. CHEMICAL REVIEWSa
  159709. GABRIEL WEATHERHEAD
  159710. 9018N
  159711. 2/28/96V
  159712. A REVIEW. HALL, H. K., JR.; EL SHEKELL, A. ANTI BREDT BRIDGEHEAD NITROGEN COMPOUNDS IN RING OPENING POLYMERIZATION. 1983, 83, 549. CHEMICAL REVIEWSa
  159713. GABRIEL WEATHERHEAD
  159714. 9019N
  159715. 2/28/96
  159716. VYA REVIEW.  RAU, H. ASYMMETRIC PHOTOCHEMISTRY IN SOLUTION. 1983, 83, 535. CHEMICAL REVIEWSa
  159717. GABRIEL WEATHERHEAD
  159718. 9020N
  159719. 2/28/96VAA REVIEW. LEWARS, E. G. OXIRENES. 1983, 83, 519. CHEMICAL REVIEWSa
  159720. GABRIEL WEATHERHEAD
  159721. 9021N
  159722. 2/28/96V
  159723. A REVIEW.  BALLAH, V.; JEYARAMAN, R.; CHANDRASEKARAN, L. SYNTHESIS OF 2,6 DISUBSTITUTED PIPERIDINES, OXANES, AND THIANES. 1983, 83, 379. CHEMICAL REVIEWSa
  159724. GABRIEL WEATHERHEAD
  159725. 9022N
  159726. 2/28/96V
  159727. A REVIEW. SMITH, H. E. THE SALICYLIDENAMINO CHIRALITY RULE: A METHOD FOR THE ESTABLISHMENT OF THE ABSOLUTE CONFIGURATIONS OF CHIRAL PRIMARY AMINES BY CIRCULAR DICHROISM. 1983, 83, 359. CHEMICAL REVIEWSa
  159728. GABRIEL WEATHERHEAD
  159729. 9023N
  159730. 2/28/96V
  159731. A REVIEW.  COOPER, A. J. L.; GINOS, J. Z.; MEISTER, A. SYNTHESIS AND PROPERTIES OF THE A KETO ACIDS. 1983, 83, 321. CHEMICAL REVIEWSa
  159732. GABRIEL WEATHERHEAD
  159733. 9024N
  159734. 2/28/96
  159735. A REVIEW. SMADJA, W. ELECTROPHILIC ADDITION TO ALLENIC DERIVATIVES:  CHEMO , REGIO , AND STEREOCHEMISTRY AND MECHANISMS. 1983, 83, 263. CHEMICAL REVIEWSa
  159736. GABRIEL WEATHERHEAD
  159737. 9025N
  159738. 2/28/96VaA REVIEW. FREEMAN, J. P. D4 ISOXAZOLINES (2,3 DIHYDROISOXAZOLES). 1983, 83, 241. CHEMICAL REVIEWSa
  159739. GABRIEL WEATHERHEAD
  159740. 9026N
  159741. 2/28/96V
  159742. A REVIEW. GLESE, B. FORMATION OF CC BONDS BY ADDITION OF FREE RADICALS TO ALKENES. 1983, 22, 753. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159743. GABRIEL WEATHERHEAD
  159744. 9027N
  159745. 2/28/96V
  159746. A REVIEW. VANE, J. R. ADVENTURES AND EXCURSIONS IN BIOASSAY: THE STEPPING STONES IN PROSTACYCLIN. 1983, 22, 741. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159747. GABRIEL WEATHERHEAD
  159748. 9028N
  159749. 2/28/96
  159750. A REVIEW.  SCHILDKNECHT, H. TURGORINS. HORMONES OFTHEENDOGENEOUS DAILY RHYTHMS OF HIGHER ORGANIZED PLANTS
  159751.  DETECTION, ISOLATION, STRUCTURE, SYNTHESIS, AND ACTIVITY. 1983, 22, 695. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159752. GABRIEL WEATHERHEAD
  159753. 9029N
  159754. 2/28/96V
  159755. A REVIEW. QUINKERT, G.; STARK, H. STEREOSELECTIVE SYNTHESIS OF ENANTIOMERICALLY PURE NATURAL PRODUCTS. 1983, 22, 637. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159756. GABRIEL WEATHERHEAD
  159757. 9030N
  159758. 2/28/96V
  159759. A REVIEW. CAUBERE, P. COMPLEX REDUCING AGENTS (CRA'S)
  159760.  VERSATILE, NOVEL WAYS OF USING SODIUM HYDRIDE IN ORGANIC SYNTHESIS [NEW SYNTHETIC METHODS (39)]. 1983, 22, 599. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159761. GABRIEL WEATHERHEAD
  159762. 9031N
  159763. 2/28/96
  159764. A REVIEW.  ADAM, W.; CILENTO, G. FOUR MEMBERED RING PEROXIDES AS EXCITED STATE EQUIVALENTS: A NEW DIMENSION IN BIOORGANIC CHEMISTRY. 1983, 22, 529. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159765. GABRIEL WEATHERHEAD
  159766. 9032N
  159767. 2/28/96V
  159768. A REVIEW. WEBER, L. METAL COMPLEXES OF SULFUR YLIDES: COORDINATION CHEMISTRY, PREPARATIVE ORGANIC CHEMISTRY, AND BIOCHEMISTRY. 1983, 22, 516. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159769. GABRIEL WEATHERHEAD
  159770. 9033N
  159771. 2/28/96V
  159772. A REVIEW. STAHL, E. A QUARTER CENTURY OF THIN LAYER CHROMATOGRAPHY
  159773. AN INTERIM REPORT. 1983, 22, 507. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLIGHa
  159774. GABRIEL WEATHERHEAD
  159775. 9034N
  159776. 2/28/96V
  159777. A REVIEW.  BEHRENS, C. H. NEW TRANSFORMATIONS OF 2,3 EPOXY ALCOHOLS AND RELATED DERIVATIVES. EASY ROUTES TO HOMOCHIRAL SUBSTANCES. 1983,16, 67. ALDRICHIMICA ACTAa
  159778. GABRIEL WEATHERHEAD
  159779. 9035N
  159780. 2/28/96
  159781. VdA REVIEW. GILL, S. K. NEW DEVELOPMENTS IN CHEMILUMINESCENCE RESEARCH. 1983,16, 59. ALDRICHIMICA ACTAa
  159782. GABRIEL WEATHERHEAD
  159783. 9036N
  159784. 2/28/96VXA REVIEW. CROCKETT, G. C. THE CHEMICAL SYNTHESIS OF DNA. 1983, 16, 47. ALDRICHIMICA ACTAa
  159785. GABRIEL WEATHERHEAD
  159786. 9037N
  159787. 2/28/96
  159788. A REVIEW.  VLIEGENIHARI, J. F. G.; DORLAND, L.; VAN HALBEEK, H. HIGH RESOLUTION, 1H NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY AS A TOOL IN THE STRUCTURAL ANALYSIS OF CARBOHYDRATES RELATED TO GLYCOPROTEINS. 1983, 41, 209. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY
  159789. GABRIEL WEATHERHEAD
  159790. 9038N
  159791. 2/28/96V
  159792. A REVIEW. BARRETO BERGTER, E.; CORIN, P. A. J. STRUCTURAL CHEMISTRY OF POLYSACCHARIDES FROM FUNGI AND LICHENS. 1983, 41, 68. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  159793. GABRIEL WEATHERHEAD
  159794. 9039N
  159795. 2/28/96
  159796. A REVIEW. BOCK, K.; PEDERSEN, C. CARBON 13 NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY OF MONOSACCHARIDES. 1983, 41, 27 ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  159797. GABRIEL WEATHERHEAD
  159798. 9040N
  159799. 2/28/96V|A REVIEW. WAGNER, P. J. CONFORMATIONAL FLEXIBILITY AND PHOTOCHEMISTRY. 1983,16, 461. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159800. GABRIEL WEATHERHEAD
  159801. 9041N
  159802. 2/28/96V
  159803. A REVIEW. WALLING, C. AN INNOCENT BYSTANDER LOOKS AT THE 2 NORBORNYL CATION. 1983,16, 448. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159804. GABRIEL WEATHERHEAD
  159805. 9042N
  159806. 2/28/96V
  159807. A REVIEW. OLAH, G. A., PRAKASH, G. K. S., SAUNDERS, M. CONCLUSION OF THE CLASSICAL NONCLASSICAL ION CONTROVERSY BASED ON THE STRUCTURAL STUDY OF THE 2 NORBORNYL CATION. 1983,16, 440. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159808. GABRIEL WEATHERHEAD
  159809. 9043N
  159810. 2/28/96
  159811. A REVIEW.  BROWN, H. C. THE ENERGY OF THE TRANSITION STATES AND THE INTERMEDIATE CATION IN THE IONIZATION OF 2 NORBORNYL DERIVATIVES. WHERE IS THE NONCLASSICAL STABILIZATION ENERGY? 1983,16, 432. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159812. GABRIEL WEATHERHEAD
  159813. 9044N
  159814. 2/28/96VvA REVIEW. GROB, C. A. INDUCTIVITY AND BRIDGING IN CARBOCATIONS. 1983, 16, 426. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159815. GABRIEL WEATHERHEAD
  159816. 9045N
  159817. 2/28/96VqA REVIEW. STEC, W. J. WADSWORTH EMMONS REACTION REVISITED. 1983, 16, 411. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159818. GABRIEL WEATHERHEAD
  159819. 9046N
  159820. 2/28/96V~A REVIEW. MCMURRY, J. E. TITANIUM INDUCED DICARBONYL COUPLING REACTIONS. 1983,16, 405. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159821. GABRIEL WEATHERHEAD
  159822. 9047N
  159823. 2/28/96V
  159824. A REVIEW. HUFFMAN, J. W. METAL AMMONIA REDUCTIONS OF CYCLIC ALIPHATIC KETONES. 1983,16, 399. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159825. GABRIEL WEATHERHEAD
  159826. 9048N
  159827. 2/28/96V
  159828. A REVIEW. MCCLELLAND, R. A.; SANTRY, L. J. REACTIVITY OF TETRAHEDRAL INTERMEDIATES. 1983,16, 394. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159829. GABRIEL WEATHERHEAD
  159830. 9049N
  159831. 2/28/96V
  159832. A REVIEW. PROSS, A.; SHAIK, S. S. A QUALITATIVE VALENCE BOND APPROACH TO ORGANIC REACTIVITY. 1983,16, 363. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159833. GABRIEL WEATHERHEAD
  159834. 9050N
  159835. 2/28/96V
  159836. A REVIEW.  BACKVALL, J. E. PALLADIUM IN SOME SELECTIVE OXIDATION REACTIONS. 1983,16, 335. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159837. GABRIEL WEATHERHEAD
  159838. 9051N
  159839. 2/28/96V
  159840. A REVIEW. GLEITER, R.; PAQUETTE, L. A. S/P INTERACTION AS A CONTROLLING FACTOR IN THE STEREOSELECTIVITY OF ADDITION REACTIONS. 1983, 16, 328. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159841. GABRIEL WEATHERHEAD
  159842. 9052N
  159843. 2/28/96
  159844. A REVIEW. ALDER, R. W. MEDIUM RING BICYCLIC COMPOUNDS AND INTRABRIDGEHEAD CHEMISTRY. 1983,16, 321. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159845. GABRIEL WEATHERHEAD
  159846. 9053N
  159847. 2/28/96V
  159848. A REVIEW. FOX, M. A. ORGANIC HETEROGENEOUS PHOTOCATALYSIS: CHEMICAL CONVERSIONS SENSITIZED BY IRRADIATED SEMICONDUCTORS. 1983, 16, 314. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159849. GABRIEL WEATHERHEAD
  159850. 9054N
  159851. 2/28/96V
  159852. A REVIEW. RUBINOVITZ, M.; WILLNER, I.; MINSKY, A. FROM CHARGED TO SUPER CHARGED SYSTEMS: THE PROBLEM OF  AROMATICITY  IN POLYCYCLIC LONS. 1983,16, 298. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159853. GABRIEL WEATHERHEAD
  159854. 9055N
  159855. 2/28/96V
  159856. A REVIEW. TOPSOM, R. D. CONTRIBUTION OF THEORETICAL CHEMISTRY TO AN UNDERSTANDING OF ELECTRONIC SUBSTITUENT EFFECTS. 1983 16, 292. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159857. GABRIEL WEATHERHEAD
  159858. 9056N
  159859. 2/28/96
  159860. VvA REVIEW.  WUBBELS, G. G. CATALYSIS OF PHOTOCHEMICAL REACTIONS. 1983, 16, 285. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159861. GABRIEL WEATHERHEAD
  159862. 9057N
  159863. 2/28/96V
  159864. A REVIEW. GASSMAN, P. G. TIDWELL, T. T. ELECTRON DEFICIENT CARBOCATIONS. 1983, 16, 279. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  159865. GABRIEL WEATHERHEAD
  159866. 9058N
  159867. 2/28/96VMA REVIEW. WENTRUP C. REACTIVE MOLECULES. WILEY INTERSCIENCE:  NEW YORK, 1984.a
  159868. GABRIEL WEATHERHEAD
  159869. 9059N
  159870. 2/28/96VlA REVIEW.  WATTHEY, J. W. H.; STANTON, J.; PEET, N. P. AZEPINES, PART 2. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159871. GABRIEL WEATHERHEAD
  159872. 9060N
  159873. 2/28/96VkA REVIEW. TABER, D. F. INTRAMOLECULAR DIELS ALDER AND ALDER ENE REACTIONS. SPRINGER VERLAG: NEW YORK, 1984.a
  159874. GABRIEL WEATHERHEAD
  159875. 9061N
  159876. 2/28/96VrA REVIEW.  ROBERTS, R. M., KHALAF, A. A. FRIEDEL CRAFTS ALKYLATION CHEMISTRY. MARCEL DEKKER, INC.: NEW YORK, 1984.a
  159877. GABRIEL WEATHERHEAD
  159878. 9062N
  159879. 2/28/96VhA REVIEW. RENFROE, B.; HARRINGTON, C.; PROCTOR, G. AZEPINES, PART 1. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159880. GABRIEL WEATHERHEAD
  159881. 9063N
  159882. 2/28/96VmA REVIEW.  RAHMAN, A U.; BASHA, A. BIOSYNTHESIS OF INDOLE ALKALOIDS. OXFORD UNIVERSITY PRESS: NEW YORK, 1983.a
  159883. GABRIEL WEATHERHEAD
  159884. 9064N
  159885. 2/28/96VvA REVIEW. OAE, S.; FURUKAWA, N. SULFILIMINES AND RELATED DERIVATIVES. AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1984.a
  159886. GABRIEL WEATHERHEAD
  159887. 9065N
  159888. 2/28/96VhA REVIEW. LINDBERG, T., ED. STRATEGIES AND TACTICS IN ORGANIC SYNTHESIS. ACADEMIC PRESS: NEW YORK, 1984.a
  159889. GABRIEL WEATHERHEAD
  159890. 9066N
  159891. 2/28/96VyA REVIEW. KIRBY, A. J. THE ANOMERIC EFFECT AND RELATED STEREOELECTRONIC EFFECTS AT OXYGEN. SPRINGER VERLAG: BERLIN, 1983.a
  159892. GABRIEL WEATHERHEAD
  159893. 9067N
  159894. 2/28/96
  159895. A REVIEW.  HOUT, JR., R. F.; HEHRE, W. J.; PIETRO, W. J. A PICTORIAL APPROACH TO MOLECULAR STRUCTURE AND REACTIVITY. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159896. GABRIEL WEATHERHEAD
  159897. 9068N
  159898. 2/28/96V
  159899. A REVIEW. DESIMONI, G.; TACCONI, G.; BARCO, A.; POLLINI, G. P. NATURAL PRODUCTS SYNTHESIS THROUGH PERICYCLIC REACTIONS. AMERICAN CHEMICAL SOCIETY: NEW YORK, 1983.a
  159900. GABRIEL WEATHERHEAD
  159901. 9069N
  159902. 2/28/96V
  159903. A REVIEW.  COLQUHOUN, H. M.; HOLTON, J.; THOMPSON, D. J.; TWIGG M. V. NEW PATHWAYS FOR ORGANIC SYNTHESIS. PLENUM: NEW YORK, 1984.a
  159904. GABRIEL WEATHERHEAD
  159905. 9070N
  159906. 2/28/96VlA REVIEW. CARPENTER, B. K. DETERMINATION OF ORGANIC REACTION MECHANISMS. WILEY INTERSCIENCE: NEW YORK, 1984.a
  159907. GABRIEL WEATHERHEAD
  159908. 9071N
  159909. 2/28/96V
  159910. A REVIEW. BARTMANN, W., TROST, B. M., EDS. SELECTIVITY A GOAL FOR SYNTHETIC EFFICIENCY. VERLAG CHEMIE: DEERFIELD BEACH, FL, 1983.a
  159911. GABRIEL WEATHERHEAD
  159912. 9072N
  159913. 2/28/96
  159914. A REVIEW. DURST, T. TECHNIQUES IN CARBANION CHEMISTRY. COMPREHENSIVE CARBANION CHEMISTRY, PART B: SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1984.a
  159915. GABRIEL WEATHERHEAD
  159916. 9073N
  159917. 2/28/96V
  159918. A REVIEW.  HEATHCOCK, C. H. STEREOSELECTIVE ALDOL CONDENSATION. COMPREHENSIVE CARBANION CHEMISTRY, PART B: SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1984.a
  159919. GABRIEL WEATHERHEAD
  159920. 9074N
  159921. 2/28/96V
  159922. A REVIEW. EPSZTEIN, R. THE FORMATION AND TRANSFORMATION OF ALLENIC A ACETYLENIC CARBANIONS. COMPREHENSIVE CARBANION CHEMISTRY, PART B: SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1984.a
  159923. GABRIEL WEATHERHEAD
  159924. 9075N
  159925. 2/28/96
  159926. A REVIEW. FRASER, R. R. THE SYN EFFECT AND THE USE OF ENOLATE EQUIVALENTS IN SYNTHESIS. COMPREHENSIVE CARBANION CHEMISTRY, PART B: SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1984.a
  159927. GABRIEL WEATHERHEAD
  159928. 9076N
  159929. 2/28/96V
  159930. A REVIEW.  HEGEDUS, L. S. FORMATION OF CARBON CARBON BONDS VIA 7R ALLYL COMPLEXES OF TRANSITION METAL. COMPREHENSIVE CARBANION CHEMISTRY, PART B: SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1984.a
  159931. GABRIEL WEATHERHEAD
  159932. 9077N
  159933. 2/28/96V
  159934. A REVIEW.  HILL, R. K. CHIRALITY TRANSFER VIA SIGMATROPIC REARRANGEMENTS. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159935. GABRIEL WEATHERHEAD
  159936. 9078N
  159937. 2/28/96V
  159938. A REVIEW. PAQUETTE, L. A. ASYMMETRIC CYCLOADDITION REACTIONS. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159939. GABRIEL WEATHERHEAD
  159940. 2/28/96V
  159941. A REVIEW. BARTLETT, P. A. OLEFIN CYCLIZATION PROCESSES THAT FORM CARBON CARBON BONDS. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159942. GABRIEL WEATHERHEAD
  159943. 9081N
  159944. 2/28/96VwA REVIEW. ENDERS, D. ALKYLATION OF CHIRAL HYDRAZONES. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159945. GABRIEL WEATHERHEAD
  159946. 9082N
  159947. 2/28/96V
  159948. A REVIEW. LUTOMSKI, K. A.; MEYERS, A. I. ASYMMETRIC SYNTHESIS VIA CHIRAL OXAZOLINES. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159949. GABRIEL WEATHERHEAD
  159950. 9083N
  159951. 2/28/96VyA REVIEW. HEATHCOCK, C. H. THE ALDOL ADDITION REACTION. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159952. GABRIEL WEATHERHEAD
  159953. 9084N
  159954. 2/28/96V
  159955. A REVIEW. EVANS, D. A. STEREOSELECTIVE ALKYLATION REACTIONS OF CHIRAL METAL ENOLATES. VOLUME 3, STEREODIFFERENTINTING ADDITION REACTIONS, PART B, 1984.a
  159956. GABRIEL WEATHERHEAD
  159957. 9085N
  159958. 2/28/96V
  159959. A REVIEW. BERGBRETTER, D. E.; NEWCOMB, M. ALKYLATION OF IMINE AND ENAMINE SALTS. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159960. GABRIEL WEATHERHEAD
  159961. 9086N
  159962. 2/28/96V
  159963. A REVIEW. POSNER, G. H. ADDITION OF ORGANOMETALLIC REAGENTS TO CHIRAL VINYLIC SULFOXIDES. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159964. GABRIEL WEATHERHEAD
  159965. 9087N
  159966. 2/28/96V
  159967. A REVIEW. TOMIOKA, K.; KOGA, K. NONCATALYTIC ADDITIONS TO Q,DUNSATURATED CARBONYL COMPOUNDS. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159968. GABRIEL WEATHERHEAD
  159969. 9088N
  159970. 2/28/96V
  159971. A REVIEW. SOLLADIE, G. ADDITION OF CHIRAL NUCLEOPHILES TO ALDEHYDES AND KETONES. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159972. GABRIEL WEATHERHEAD
  159973. 9089N
  159974. 2/28/96
  159975. A REVIEW. ELIEL, E. L. APPLICATION OF CRAM'S RULE: ADDITION OF ACHIRAL NUCLEOPHILES TO CHIRAL SUBSTRATES. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159976. GABRIEL WEATHERHEAD
  159977. 9090N
  159978. 2/28/96V
  159979. A REVIEW. INOUYE, Y. ODA, J.  BABA, N. REDUCTIONS WITH CHIRAL DIHYDROPYRIDINE REAGENTS. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159980. GABRIEL WEATHERHEAD
  159981. 9091N
  159982. 2/28/96V
  159983. A REVIEW. GRANDBOIS, E. R., HOWARD, S. I.; MORRISON, J. D. REDUCTIONS WITH CHIRAL MODIFICATIONS OF LITHIUM ALUMINUM HYDRIDE. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159984. GABRIEL WEATHERHEAD
  159985. 9092N
  159986. 2/28/96V
  159987. A REVIEW. MIDLAND, M. M. REDUCTIONS WITH CHIRAL BORON REAGENTS. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159988. GABRIEL WEATHERHEAD
  159989. 9093N
  159990. 2/28/96
  159991. A REVIEW. BROWN, H. C., JADHAV, P. K. ASYMMETRIC HYDROBORATION. VOLUME 2. STEREODIFFERENTIATING ADDITION REACTIONS, PART A, 1983.a
  159992. GABRIEL WEATHERHEAD
  159993. 9094N
  159994. 2/28/96V
  159995. A REVIEW. FRASER, R. R. NUCLEAR MAGNETIC RESONANCE ANALYSIS USING CHIRAL SHIFT REAGENTS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  159996. GABRIEL WEATHERHEAD
  159997. 9095N
  159998. 2/28/96V
  159999. A REVIEW. WEISMAN, G. R. NUCLEAR MAGNETIC RESONANCE ANALYSIS USING CHIRAL SOLVATING AGENTS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160000. GABRIEL WEATHERHEAD
  160001. 9096N
  160002. 2/28/96V
  160003. A REVIEW. YAMAGUCHI, S. NUCLEAR MAGNETIC RESONANCE ANALYSIS USING CHIRAL DERIVATIVES. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160004. GABRIEL WEATHERHEAD
  160005. 9097N
  160006. 2/28/96
  160007. A REVIEW. PIRKLE, W. H., FINN, J. SEPARATION OF ENANTIOMERS BY LIQUID CHROMATOGRAPHIC METHODS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160008. GABRIEL WEATHERHEAD
  160009. 9098N
  160010. 2/28/96V
  160011. A REVIEW. SCHURIG, V. GAS CHROMATOGRAPHIC METHODS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160012. GABRIEL WEATHERHEAD
  160013. 9099N
  160014. 2/28/96V
  160015. A REVIEW. ANDERSEN, K. K., GASH, D. M.; ROBERTSON, J. D. ISOTOPE DILUTION TECHNIQUES. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160016. GABRIEL WEATHERHEAD
  160017. 9100N
  160018. 2/28/96V
  160019. A REVIEW. SCHOOFS, A. R.; GUETTE, J. P. COMPETITIVE REACTION METHODS FOR THE DETERMINATION OF MAXIMUM SPECIFIC ROTATIONS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160020. GABRIEL WEATHERHEAD
  160021. 9101N
  160022. 2/28/96V
  160023. A REVIEW. LYLE, G. G.  LYLE, R. E. POLARIMETRY. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160024. GABRIEL WEATHERHEAD
  160025. 9102N
  160026. 2/28/96V
  160027. A REVIEW. MORRISON, J. D. A SUMMARY OF WAYS TO OBTAIN OPTICALLY ACTIVE COMPOUNDS. ASYMMETRIC SYNTHESIS, J. D. MORRISON, ED., ACADEMIC PRESS: NEW YORK. VOLUME 1. ANALYTICAL METHODS, 1983.a
  160028. GABRIEL WEATHERHEAD
  160029. 9103N
  160030. 2/28/96V
  160031. A REVIEW.  MAAT, L.; BEYERMAN, H. C. THE IMIDAZOLE ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 22, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  160032. GABRIEL WEATHERHEAD
  160033. 9104N
  160034. 2/28/96V
  160035. A REVIEW. NINOMIYA, I.; NAITO, T. THE APPLICATION OF ENAMIDE CYCLIZATION IN ALKALOID SYNTHESIS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 22, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  160036. GABRIEL WEATHERHEAD
  160037. 9105N
  160038. 2/28/96
  160039. A REVIEW. GUGGISBERG, A.  HESSE, M. PUTRESCINE, SPERMIDINE, SPERMINE, AND RELATED POLYAMINE ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 22, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  160040. GABRIEL WEATHERHEAD
  160041. 9106N
  160042. 2/28/96V
  160043. A REVIEW. KARLE, I. L. ELUCIDATION OF STRUCTURAL FORMULA, CONFIGURATION AND CONFORMATION OF ALKALOIDS BY X RAY DIFFRACTION. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 22, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  160044. GABRIEL WEATHERHEAD
  160045. 9107N
  160046. 2/28/96V
  160047. A REVIEW. FUJII, T.; OHBA, M. IPECAC ALKALOIDS AND B CARBOLINE CONGENERS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 22, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1983.a
  160048. GABRIEL WEATHERHEAD
  160049. 9108N
  160050. 2/28/96VtA REVIEW. BALDWIN, J. E.; PERLMUTTER P. BRIDGED, CAPPED AND FENCED PORPHYRINS. 1984,12I. TOPICS IN CURRENT CHEMISTRYa
  160051. GABRIEL WEATHERHEAD
  160052. 9109N
  160053. 2/28/96
  160054. A REVIEW.  KADEN, T. A. SYNTHESIS AND METAL COMPLEXES OF AZAMACROCYCLES WITH PENDANT ARMS HAVING ADDITIONAL LIGATING GROUPS. 1984, 121. TOPICS IN CURRENT CHEMISTRYa
  160055. GABRIEL WEATHERHEAD
  160056. 9110N
  160057. 2/28/96VjA REVIEW. SMID, J.; SINTA R. MACROHETEROCYCLIC LIGANDS ON POLYMERS. 1984, 121. TOPICS IN CURRENT CHEMISTRYa
  160058. GABRIEL WEATHERHEAD
  160059. 9111N
  160060. 2/28/96V
  160061. A REVIEW. SHINKAI, S.; MANABE, 0. PHOTOCONTROL OF ION EXTRACTION AND ION TRANSPORT BY PHOTOFUNCTIONAL CROWN ETHERS. 1984, 121 TOPICS IN CURRENT CHEMISTRYa
  160062. GABRIEL WEATHERHEAD
  160063. 9112N
  160064. 2/28/96V
  160065. A REVIEW. TAKAGI, M.  UENO K. CROWN COMPOUNDS AS ALKALI AND ALKALINE EARTH METAI ION SELECTIVE CHROMOGENIC REAGENTS. 1984, 121. TOPICS IN CURRENT CHEMISTRYa
  160066. GABRIEL WEATHERHEAD
  160067. 9113N
  160068. 2/28/96VtA REVIEW.  TAKEDA, Y. THE SOLVENT EXTRACTION OF METAL IONS BY CROWN COMPOUNDS. 1984,121. TOPICS IN CURRENT CHEMISTRYa
  160069. GABRIEL WEATHERHEAD
  160070. 2/28/96V{A REVIEW. PAQUETTE, L. A. RECENT SYNTHETIC DEVELOPMENTS IN POLYQUINANE  CHEMISTRY. 1984, I L 9. TOPICS IN CURRENT CHEMISTRYa
  160071. GABRIEL WEATHERHEAD
  160072. 9115N
  160073. 2/28/96VlA REVIEW.  SHUBIN, V. G. REARRANGEMENTS OF CARBOCATIONS BY 1,2SHIFTS. 1984, 117. TOPICS IN CURRENT CHEMISTRYa
  160074. GABRIEL WEATHERHEAD
  160075. 9116N
  160076. 2/28/96VYA REVIEW. BARKASH, V. A. NONCLASSICAL CARBOCATIONS. 1984,116. TOPICS IN CURRENT CHEMISTRYa
  160077. GABRIEL WEATHERHEAD
  160078. 9117N
  160079. 2/28/96V|A REVIEW. LIU, R. S. H.; ASATO, A. E. PHOTOCHEMISTRY AND SYNTHESIS OF STEREOIGOMERS OF VITAMIN A. 1984, 40,1931. TETRAHEDRONa
  160080. GABRIEL WEATHERHEAD
  160081. 9118N
  160082. 2/28/96VkA REVIEW. LINDLEY, J. COPPER ASSISTED NUCLEOPHILIC SUBSTITUTION OF ARYL HALOGEN. 1984, 40,1433. TETRAHEDRONa
  160083. GABRIEL WEATHERHEAD
  160084. 9119N
  160085. 2/28/96
  160086. A REVIEW. FERRIS, J. P. HAGAN, JR. W. J. HCN AND CHEMICAL EVOLUTION: THE POSSIBLE ROLE OF CYANO COMPOUNDS IN PREBIOTIC SYNTHESIS. 1984, 40,1093. TETRAHEDRONa
  160087. GABRIEL WEATHERHEAD
  160088. 9120N
  160089. 2/28/96VlA REVIEW. BAIZER, M. M. RECENT DEVELOPMENTS IN ORGAMIC SYNTHESIS BY ELECTROLYSIS. 1984, 40, 935. TETRAHEDRONa
  160090. GABRIEL WEATHERHEAD
  160091. 9121N
  160092. 2/28/96V]A REVIEW. SHONO, T. ELECTROORGANIC CHEMISTRY IN ORGANIC SYNTHESIS. 1984, 40, 811. TETRAHEDRONa
  160093. GABRIEL WEATHERHEAD
  160094. 9122N
  160095. 2/28/96VuA REVIEW.  ERDIK, E. COPPER(I) CATALYZED REACTIONS OF ORGANOLITHIUM AND GRIGNARD REAGENTS. 1984, 40, 641. TETRAHEDRONa
  160096. GABRIEL WEATHERHEAD
  160097. 9123N
  160098. 2/28/96V]A REVIEW.  TABUSHI, I. DESIGN AND SYNTHESIS OF ARTIFICIAL ENZYMES. 1984, 40, 269. TETRAHEDRONa
  160099. GABRIEL WEATHERHEAD
  160100. 9124N
  160101. 2/28/96
  160102. A REVIEW. NEWTON, R. F., ROBERTS, S. M.; TAYLOR, R. J. K. STRATEGIES EMPLOYED IN THE SYNTHESIS OF PROSTACYCLINS AND THROMBOXANES. 1984, 449. SYNTHESISa
  160103. GABRIEL WEATHERHEAD
  160104. 9125N
  160105. 2/28/96VAA REVIEW. AGER, D. J. THE PETERSON REACTION. 1984, 384. SYNTHESISa
  160106. GABRIEL WEATHERHEAD
  160107. 9126N
  160108. 2/28/96V{A REVIEW. TSUJI, J. SYNTHETIC APPLICATIONS OF THE PALLADIUM CATALYZED OXIDATION OF OLEFINS TO KETONES. 1984, 369. SYNTHESISa
  160109. GABRIEL WEATHERHEAD
  160110. 9127N
  160111. 2/28/96V
  160112. A REVIEW.  HEWLINS, M. J. E.; OLIVEIRA CAMPOS, A. M.; SHANNON, P. V. R. SYNTHETIC APPROACHES TO ELLIPTICINES AND OTHER DERIVATIVES AND ANALOGUES OF 6H PYRIDO[4,3 B]CARBAZOLE. 1984, 289. SYNTHESISa
  160113. GABRIEL WEATHERHEAD
  160114. 9128N
  160115. 2/28/96VbA REVIEW.  ZAUGG, H. E. A AMIDOALKYLATION AT CARBON: RECENT ADVANCES PART II. 1984, 181. SYNTHESISa
  160116. GABRIEL WEATHERHEAD
  160117. 9129N
  160118. 2/28/96
  160119. -V`A REVIEW.  ZAUGG, H. E. A AMIDOALKYLATION AT CARBON: RECENT ADVANCES PART I. 1984, 85. SYNTHESISa
  160120. GABRIEL WEATHERHEAD
  160121. 9130N
  160122. 2/28/96V{A REVIEW. ELNAGDI, M. H.; ELMOGHAYAR, M. R. H.; ELGEMEIE, G. E. H. THE CHEMISTRY OF 3 0XOALKANENITRILES. 1984, 1. SYNTHESISa
  160123. GABRIEL WEATHERHEAD
  160124. 9131N
  160125. 2/28/96V
  160126. A REVIEW.  NARISIMBAN, N. S., MALI, R. S. SYNTHESES OF HETEROCYCLIC COMPOUNDS INVOLVING AROMATIC LITHIATION REACTIONS IN THE KEY STEP. 1983, 957. SYNTHESISa
  160127. GABRIEL WEATHERHEAD
  160128. 9132N
  160129. 2/28/96VvA REVIEW. BUCKUS, P. THE DEBENZHYDRYLATION AND TRANSBENZHYDRYLATION REACTIONS. 1983, 52,1203. RUSSIAN CHEMICAL REVIEWSa
  160130. GABRIEL WEATHERHEAD
  160131. 9133N
  160132. 2/28/96V
  160133. A REVIEW. SVEDA, V., GALAEV, I. U. ENZYMIC CONVERSION OF RACEMATES INTO AMINOACID ENANTIOMERS. 1983, 52,1184. RUSSIAN CHEMICAL REVIEWSa
  160134. GABRIEL WEATHERHEAD
  160135. 9134N
  160136. 2/28/96
  160137. A REVIEW. RAEVSKII, 0. A.; IGNAT'EVA, T. I. CONFORMATIONAL ANALYSIS OF PHOSPHORYL COMPOUNDS WITH PHOSPHORUS CARBON BONDS. 1983, 52, 1156. RUSSIAN CHEMICAL REVIEWSa
  160138. GABRIEL WEATHERHEAD
  160139. 9135N
  160140. 2/28/96VqA REVIEW. PETROV, E. S. THE EQUILIBRIUM NH ACIDITY OF ORGANIC COMPOUNDS. 1983, 52, 1144. RUSSIAN CHEMICAL REVIEWSa
  160141. GABRIEL WEATHERHEAD
  160142. 9136N
  160143. 2/28/96V~A REVIEW. KOLODYAZHNYI 0. I.; KUKHAR', V. P. P; HETERO SUBSTITUTED PHOSPHORUS YLIDES. 1983, 52, 1096. RUSSIAN CHEMICAL REVIEWSa
  160144. GABRIEL WEATHERHEAD
  160145. 9137N
  160146. 2/28/96V
  160147. A REVIEW. VERESHECHAGIN, A. N. CONFORMATIONS OF SIX MEMBERED CARBON RINGS WITH PLANAR GROUPS. 1983, 52,1081. RUSSIAN CHEMICAL REVIEWSa
  160148. GABRIEL WEATHERHEAD
  160149. 9138N
  160150. 2/28/96V~A REVIEW. KONOVALOV, A. I. THE REACTIVITY OF ADDENDS IN THE DIENE SYNTHESIS REACTION. 1983, 52, 1064. RUSSIAN CHEMICAL REVIEWSa
  160151. GABRIEL WEATHERHEAD
  160152. 9139N
  160153. 2/28/96
  160154. A REVIEW. PETROV, A. A., DOGADINA, A. V., IONIN, B. I.; GARIBINA, V. A.; LEONOV, A. A. THE ARBUZOV REARRANGEMENT WITH PARTICIPATION OF HALOGENOACETYLENES AS A METHOD OF SYNTHESIS OF ETHYNYLPHOSPHONATES AND OTHER ORGANOPHOSPHORUS COMPOUNDS. 1983, 52, 1030. RUSSIAN CHEMICAL REVIEWS
  160155. GABRIEL WEATHERHEAD
  160156. 9140N
  160157. 2/28/96V
  160158. A REVIEW. MASTRYUKOVA, T. A.; KABACHNIK, M. L THE PHOSPHORUS CARBON PROTOTROPIC TAUTOMERISM. 1983, 52,1012. RUSSIAN CHEMICAL REVIEWSa
  160159. GABRIEL WEATHERHEAD
  160160. 9141N
  160161. 2/28/96V
  160162. A REVIEW. YAGUPOL'SKII, L. M.; IL'CHENKO A. YA., GANDEL'SMAN, L. Z. FLUORINE CONTAINING DYES. 1983, 52, 993. RUSSIAN CHEMICAL REVIEWSa
  160163. GABRIEL WEATHERHEAD
  160164. 9142N
  160165. 2/28/96VtA REVIEW. BAGRII, E. I.; SAGINAEV, A. T. UNSATURATED ADAMANTANE DERIVATIVES. 1983, 52, 881. RUSSIAN CHEMICAL REVIEWSa
  160166. GABRIEL WEATHERHEAD
  160167. 9143N
  160168. 2/28/96
  160169. A REVIEW. MATNISHYAN, A. A.; KOBRYANSKII, V. M. CHARACTERISTIC FEATURES OF THE POLYMERISATION OF ACETYLENE AND ITS DERIVATIVES. 1983, 52, 751. RUSSIAN CHEMICAL REVIEWSa
  160170. GABRIEL WEATHERHEAD
  160171. 9144N
  160172. 2/28/96V
  160173. A REVIEW. LYUBOVSKAYA, R. N. ORGANIC METALS AND SUPERCONDUCTORS BASED ON TETRATHIOFULVALENE DERIVATIVES. 1983, 52, 736. RUSSIAN CHEMICAL REVIEWSa
  160174. GABRIEL WEATHERHEAD
  160175. 9145N
  160176. 2/28/96V
  160177. A REVIEW. MELENT'EVA, T. A. THE STRUCTURE AND REACTIVITY OF  OCTADEHYDROCORRINS AND CORROLES. 1983, 52, 641. RUSSIAN CHEMICAL REVIEWSa
  160178. GABRIEL WEATHERHEAD
  160179. 9146N
  160180. 2/28/96VwA REVIEW. PANKRATOV, V. A.; FRENKEL', TS. M.; FAINLEIB, A. M. 2 OXAZOLIDINONES. 1983, 52, 576. RUSSIAN CHEMICAL REVIEWSa
  160181. GABRIEL WEATHERHEAD
  160182. 9147N
  160183. 2/28/96V
  160184. A REVIEW.  KNUNYANTS, I. L.; SIZOV, YU. A. UKHAROV, 0. V. THE SYNTHESIS AND PROPERTIES OF ALIPHATIC FLUORONITROSO COMPOUNDS. 1983, 52, 554. RUSSIAN CHEMICAL REVIEWSa
  160185. GABRIEL WEATHERHEAD
  160186. 9148N
  160187. 2/28/96V
  160188. A REVIEW. AKHREM, I. S., CHISTOVALOVA, N. M.; VOL'PIM, M. E. THE SPLITTING OF THE SILICON CARBON BOND BY COMPOUNDS OF PLATINUM AND PALLADIUM. 1983, 52, 542. RUSSIAN CHEMICAL REVIEWSa
  160189. GABRIEL WEATHERHEAD
  160190. 9149N
  160191. 2/28/96V
  160192. A REVIEW. KICHOOM, A. P. G.; VAN BEKKUM, H. ASPECTS OF THE CHEMICAL CONVERSION OF GLUCOSE. 1984,103,1. RECUEIL: JOURNAL OF THE ROYAL NETHERLANDS CHEMICAL SOCIETYa
  160193. GABRIEL WEATHERHEAD
  160194. 9150N
  160195. 2/28/96V
  160196. A REVIEW. TAFT, R. W. PROTONIC ACIDITIES AND BASICITIES M THE GAS PHASE AND IN SOLUTION: SUBSTITUENT AND SOLVENT EFFECTS. 1983, 14, 247. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160197. GABRIEL WEATHERHEAD
  160198. 9151N
  160199. 2/28/96V
  160200. A REVIEW. SUNKO, D. E.; HEHRE, W. J. SECONDARY DEUTERIUM ISOTOPE EFFECTS ON REACTIONS PROCEEDING THROUGH CARBOCATIONS. 1983, Z4, 205. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160201. GABRIEL WEATHERHEAD
  160202. 9152N
  160203. 2/28/96
  160204. DVhA REVIEW. REYNOLDS, W. F. POLAR SUBSTITUENT EFFECTS. 1983,14,165. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160205. GABRIEL WEATHERHEAD
  160206. 9153N
  160207. 2/28/96VgA REVIEW. GALLO, R. J. TREATMENT OF STERIC EFFECTS. 1983,14,115. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160208. GABRIEL WEATHERHEAD
  160209. 9154N
  160210. 2/28/96V
  160211. A REVIEW. FUJITA, T. SUBSTITUENT EFFECTS IN THE PARTITION COEFFICIENT OF DISUBSTITUTED BENZENES: BIDIRECTIONAL HAMMETT TYPE RELATIONSHIPS. 1983,14, 75. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160212. GABRIEL WEATHERHEAD
  160213. 9155N
  160214. 2/28/96V
  160215. A REVIEW. CRAIK, D. J.; BROWNLEE, T. C. SUBSTITUENT EFFECTS ON CHEMICAL SHIFTS IN THE SIDECHAINS OF AROMATIC SYSTEMS. 1983, 14, 1. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  160216. GABRIEL WEATHERHEAD
  160217. 9156N
  160218. 2/28/96V|A REVIEW. BUCHANAN, J. G. THE C NUCLEOSIDE ANTIBIOTICS. 1984, 44, 243. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160219. GABRIEL WEATHERHEAD
  160220. 2/28/96V
  160221. A REVIEW. NAYLOR, S., HANKE, F. J.  MAMES, L. V.; CREWS, P. CHEMICAL AND BIOLOGICAL ASPECTS OF MARINE MONOTERPENES. 1984, 44, 189. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160222. GABRIEL WEATHERHEAD
  160223. 9158N
  160224. 2/28/96V
  160225. A REVIEW. MONDON, A.; EPE, B. BITTER PRINCIPLES OF CNEORACEAE. 1984, 44, 101. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160226. GABRIEL WEATHERHEAD
  160227. 9159N
  160228. 2/28/96V
  160229. A REVIEW. EVANS, F. J.; TAYLOR, S. E. PRO INFLAMMATORY, TUMOUR PROMOTING AND ANTI TUMOUR DITERPENES OF THE PLANT FAMILIES EUPHORBIACEAE AND THYMEFAEACEAE. 1984, 44,1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160230. GABRIEL WEATHERHEAD
  160231. 9160N
  160232. 2/28/96V
  160233. A REVIEW. ARSENIYADIS, S., KYLER, K. S., WATT, D. S. ADDITION AND SUBSTITUTION REACTIONS OF NITRILE STABILIZED CARBANIONS. 1984, 31. ORGANIC REACTIONSa
  160234. GABRIEL WEATHERHEAD
  160235. 9161N
  160236. 2/28/96
  160237. A REVIEW. WONG, H. N. C.; NG, T. K.; WONG, T. Y.; XING, Y. D. ARENE SYNTHESES BY DEHYDRATION OF 7 0XABICYCLO[2.2.1]HEPTENE SYSTEMS. 1984, 22, 875. HETEROCYCLESa
  160238. GABRIEL WEATHERHEAD
  160239. 9162N
  160240. 2/28/96V
  160241. A REVIEW. OHSHIRO, Y. HIRAO, T. HETEROCYCLIC SYNTHESIS BY METAL CARBONYL INDUCED CYCLIZATION REACTION. 1984, 22, 859. HETEROCYCLESa
  160242. GABRIEL WEATHERHEAD
  160243. 9163N
  160244. 2/28/96VqA REVIEW. ATTA UR RAHMAN, SULTANA, M. SYNTHETIC APPROACHES TO THE HUNTERIA ALKALOIDS. 1984, 22, 841. HETEROCYCLESa
  160245. GABRIEL WEATHERHEAD
  160246. 9164N
  160247. 2/28/96V
  160248. A REVIEW. RAKHMANKULOV, D. L.; ZORIN, V. V.; PASTUSHENKO, E. V.; ZLOTSKY, S. S. FREE RADICAL TRANSFORMATIONS OF CYCLIC ACETALS. 1984, 22, 817. HETEROCYCLESa
  160249. GABRIEL WEATHERHEAD
  160250. 9165N
  160251. 2/28/96
  160252. A REVIEW. GOVUNDACHARI, T. R.; CHINNASAMY, P.; RAJESWARI, S.; CHANDRASEKARAM, S.; PREMILA, M. S.; NATARAJAN, S.; NAGARAJAM, K.; PAI, B. R. SOME RECENT WORK ON SCHIFF BASES IMINES AND IMINIUM SALTS IN SYNTHETIC HETEROCYCLIC CHEMISTRY A REVIEW. 1984, 22, 585. HETEROCYCLES
  160253. GABRIEL WEATHERHEAD
  160254. 9166N
  160255. 2/28/96VgA REVIEW. CLARK, R. D.; REPKE, D. B. THE LEIMGRUBER BATCHO INDOLE SYNTHESIS. 1984, 22,195. HETEROCYCLESa
  160256. GABRIEL WEATHERHEAD
  160257. 9167N
  160258. 2/28/96V
  160259. A REVIEW. SEEMAN, J. I. RECENT STUDIES IN NICOTINE CHEMISTRY. COMFORMATIONAL ANALYSIS, CHEMICAL REACTIVITY STUDIES, AND THEORETICAL MODELING. 1984, 22,165. HETEROCYCLESa
  160260. GABRIEL WEATHERHEAD
  160261. 9168N
  160262. 2/28/96V
  160263. A REVIEW. BOSCH, J.; BENNASAR, M. L. ELABORATION OF THE ETHYLIDENE SUBSTITUENT IN THE SYNTHESIS OF INDOLE ALKALOIDS. 1983, 20, 2471. HETEROCYCLESa
  160264. GABRIEL WEATHERHEAD
  160265. 9169N
  160266. 2/28/96
  160267. A REVIEW. ELNAGDI, M. H.; ABDEL GALIL, F. M.; RIAD, B. Y.; ELGEMEIE, G. E. H. RECENT DEVELOPMENTS IN CHEMISTRY OF 3(5) AMINOPYRAZOLES. 1983, 20, 2437. HETEROCYCLESa
  160268. GABRIEL WEATHERHEAD
  160269. 9170N
  160270. 2/28/96VoA REVIEW. JONES, P. G. CRYSTAL STRUCTURE DETERMINATION: A CRITICAL VIEW. 1984,13, 157. CHEMICAL SOCIETY REVIEWSa
  160271. GABRIEL WEATHERHEAD
  160272. 9171N
  160273. 2/28/96VoA REVIEW. MARKOV, P. LIGHT INDUCED TAUTOMERISM OF B DICARBONYL COMPOUNDS. 1984,13, 69. CHEMICAL SOCIETY REVIEWSa
  160274. GABRIEL WEATHERHEAD
  160275. 9172N
  160276. 2/28/96V
  160277. A REVIEW.  KATRITZKY, A. R.; MUSUMARRA, G. NEW INSIGHTS INTO ALIPHATIC NUCLEOPHILIC SUBSTITUTION REACTIONS FROM THE USE OF PYRIDINES AS LEAVING GROUPS. 1984,13, 37. CHEMICAL SOCIETY REVIEWSa
  160278. GABRIEL WEATHERHEAD
  160279. 9173N
  160280. 2/28/96VlA REVIEW. SIMONETTA, M. ORGANIC REACTION PATHS: A THEORETICAL APPROACH. 1984, 13,1. CHEMICAL SOCIETY REVIEWSa
  160281. GABRIEL WEATHERHEAD
  160282. 9174N
  160283. 2/28/96
  160284. ZVVA REVIEW. VIC DISULFOXIDES AND OS SULFENYL SULFINATES. 1984, 84, 117. CHEMICAL REVIEWSa
  160285. GABRIEL WEATHERHEAD
  160286. 9175N
  160287. 2/28/96VnA REVIEW. ALBINI, A.; ALPEGIANI, M. THE PHOTOCHEMISTRY OF THE N OXIDE FUNCTION. 1984, 84, 43. CHEMICAL REVIEWSa
  160288. GABRIEL WEATHERHEAD
  160289. 9176N
  160290. 2/28/96V
  160291. A REVIEW.  JONES, B. A.; BRADSHAW, J. S. SYNTHESIS AND REDUCTION OF  CHEMICAL REVIEWS THIOCARBOXYLIC O ESTERS. 1984, 84,17. CHEMICAL REVIEWSa
  160292. GABRIEL WEATHERHEAD
  160293. 9177N
  160294. 2/28/96VgA REVIEW. LIN, T. S. ELECTRON SPIN ECHO SPECTROSCOPY OF ORGANIC TRIPLETS. 1984, 84, 1. CHEMICAL REVIEWSa
  160295. GABRIEL WEATHERHEAD
  160296. 9178N
  160297. 2/28/96V
  160298. A REVIEW. SOLLADIE, G.; ZIMMERMANN, R. G. LIQUID CRYSTALS: A TOOL FOR STUDIES ON CHIRALITY. 1984, 23, 348. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160299. GABRIEL WEATHERHEAD
  160300. 9179N
  160301. 2/28/96
  160302. A REVIEW. MEINEL, C.  ... TO MAKE CHEMISTRY MORE APPLICABLE AND GENERALLY BENEFICIAL  THE TRANSITION TO SCIENTIFIC PERSPECTIVE IN EIGHTEENTH CENTURY CHEMISTRY. 1984, 23, 339. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160303. GABRIEL WEATHERHEAD
  160304. 9180N
  160305. 2/28/96V
  160306. A REVIEW. TAUBE, H. ELECTRON TRANSFER BETWEEN METAL COMPLEXES A RETROSPECTIVE VIEW. 1984, 23, 329. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160307. GABRIEL WEATHERHEAD
  160308. 9181N
  160309. 2/28/96V
  160310. A REVIEW. LOZAC'H, N.; GOODSON, A. L. NODAL NOMENCLATURE II. SPECIFIC NOMENCLATURE FOR PARENT HYDRIDES, FREE RADICALS IONS, AND SUBSTITUENTS. L984, 23, 33. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160311. GABRIEL WEATHERHEAD
  160312. 9182N
  160313. 2/28/96VuA REVIEW. TIDWELL, T. T. DESTABILIZED CARBOCATIONS. 1984, 23, 20. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160314. GABRIEL WEATHERHEAD
  160315. 9183N
  160316. 2/28/96
  160317. A REVIEW.  HOFFMANN, H. M. R. THE CYCLOADDITION OF ALLYL CATIONS TO 1,3 DIENES: GENERAL METHODS FOR THE SYNTHESIS OF SEVEN MEMBERED CARBOCYCLES. 1984, 23,1. ANGEWANDTE CHIMIE, INTERNATIONAL EDITION IN ENGLISHa
  160318. GABRIEL WEATHERHEAD
  160319. 9184N
  160320. 2/28/96V{A REVIEW. SINGLETON, E.; OOSTHUIZEN, H. ES. METAL ISOCYANIDE COMPLEXES. 1983, 22, 209. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160321. GABRIEL WEATHERHEAD
  160322. 9185N
  160323. 2/28/96VlA REVIEW.  VAHRENKAMP, H. BASIC METAL CLUSTER REACTIONS. 1983, 22, 169. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160324. GABRIEL WEATHERHEAD
  160325. 9186N
  160326. 2/28/96V
  160327. A REVIEW. DARENSBOURG, D. J.; KUDAROSKI, R. A. THE ACTIVATION OF CARBON DIOXIDE BY METAL COMPLEXES. 1983, 22,129. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160328. GABRIEL WEATHERHEAD
  160329. 9187N
  160330. 2/28/96V
  160331. A REVIEW. BRUCE, M. I.; SWINCER A. G. VINYLIDENE AND PROPADIENYLIDENE (ALLENYLIDENE) METAL COMPLEXES. 1983, 22, 60. ADVANCES IN ORGANOMETALLIC CHEMISTRY
  160332. GABRIEL WEATHERHEAD
  160333. 9188N
  160334. 2/28/96VvA REVIEW.  BRADLEY, J. S. THE CHEMISTRY OF CARBIDOCARBONYL CLUSTERS. 1983, 22, 1. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160335. GABRIEL WEATHERHEAD
  160336. 9189N
  160337. 2/28/96V
  160338. A REVIEW. ILLUMINATI, G.; STEGEL, F. THE FORMATION OF ANIONIC SADDUCTS FROM HETEROAROMATIC COMPOUNDS: STRUCTURES, RATES, AND EQUILIBRIA. 1983, 34, 306. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160339. GABRIEL WEATHERHEAD
  160340. 9190N
  160341. 2/28/96VmA REVIEW.  KUTHAN, J. PYRANS, THIOPYRANS, AND SELENOPYRANS. I983, 34, 146. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160342. GABRIEL WEATHERHEAD
  160343. 9191N
  160344. 2/28/96V~A REVIEW. JONES, G.; SLISKOVIC, D. R. THE CHEMISTRY OF THE TRIAZOLOPYRIDINES. L983, 34, 80. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160345. GABRIEL WEATHERHEAD
  160346. 9192N
  160347. 2/28/96VlA REVIEW. SAMMES, M. P.; KATRITZKY, A. R. THE 4H PYRAZOLES. I9B3, 34, 54. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160348. GABRIEL WEATHERHEAD
  160349. 9193N
  160350. 2/28/96VkA REVIEW. SAMMES, M. P.; KATRITZKY, A. R. THE 3H PYRAZOLES. 1983, 34, 2. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160351. GABRIEL WEATHERHEAD
  160352. 9194N
  160353. 2/28/96VuA REVIEW. TABUSHI, I.; KURODA Y. CYCLODEXTRINS AND CYCLOPHANES AS ENZYME MODELS. 1983, 32, 417. ADVANCES IN CATALYSISa
  160354. GABRIEL WEATHERHEAD
  160355. 9195N
  160356. 2/28/96V
  160357. A REVIEW. DOMBEK, B. D. HOMOGENEOUS CATALYTIC HYDROGENATION OF CARBON MONOXIDE: ETHYLENE GLYCOL AND ETHANOL FROM SYNTHESIS GAS. 1983, 32, 326. ADVANCES IN CATALYSISa
  160358. GABRIEL WEATHERHEAD
  160359. 9196N
  160360. 2/28/96V
  160361. A REVIEW.  HAPPEL, J.; SELLERS, P. H. ANALYSIS OF THE POSSIBLE MECHANISMS FOR A CATALYTIC REACTION SYSTEM. 1983, 32, 274. ADVANCES IN CATALYSISa
  160362. GABRIEL WEATHERHEAD
  160363. 9197N
  160364. 2/28/96V
  160365. A REVIEW.  IZUMI, Y. MODIFIED RANEY NICKEL (MRNI) CATALYST: HETEROGENEOUS ENANTIO DIFFERENTIATING (ASYMMETRIC) CATALYST. 1983, 32, 215. ADVANCES IN CATALYSISa
  160366. GABRIEL WEATHERHEAD
  160367. 9198N
  160368. 2/28/96VgA REVIEW.  RONEC, V. CATALYSIS BY ALLOYS IN HYDROCARBON REACTIONS. 1983, 32, 149. ADVANCES IN CATALYSISa
  160369. GABRIEL WEATHERHEAD
  160370. 9199N
  160371. 2/28/96V
  160372. A REVIEW. CHE, M.; TENCH, A. J. CHARACTERIZATION AND REACTIVITY OF MOLECULAR OXYGEN SPECIES ON OXIDE SURFACES. 1983, 32, 2 ADVANCES IN CATALYSISa
  160373. GABRIEL WEATHERHEAD
  160374. 9200N
  160375. 2/28/96V
  160376. A REVIEW. WUDL, F. FROM ORGANIC METALS TO SUPERCONDUCTORS: MANAGING CONDUCTION ELECTRONS IN ORGANIC SOLIDS. 1984, 17, 227 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160377. GABRIEL WEATHERHEAD
  160378. 9201N
  160379. 2/28/96V
  160380. A REVIEW. MILSTEM, D. CIS ALKYL  AND CIS ACYLRHODIUM AND  IRIDIUM HYDRIDES: MODEL INTERMEDIATES IN HOMOGENEOUS CATALYSIS. 1984, 17, 221. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160381. GABRIEL WEATHERHEAD
  160382. 9202N
  160383. 2/28/96
  160384. A REVIEW. KABALKA, G. S. INCORPORATION OF STABLE AND RADIOACTIVE ISOTOPES VIA ORGANOBORANE CHEMISTRY. 1984,17, 215. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160385. GABRIEL WEATHERHEAD
  160386. 9203N
  160387. 2/28/96V
  160388. A REVIEW.  MEOT NER (MAUTNER), M. STRUCTURALLY COMPLEX ORGANIC IONS: THERMOCHEMISTRY AND NONCOVALENT INTERACTIONS. 1984, 17, 186. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160389. GABRIEL WEATHERHEAD
  160390. 9204N
  160391. 2/28/96V
  160392. A REVIEW. SHIDA, T.; HASELBACH, E.; BALLY, T. ORGANIC RADICAL IONS IN RIGID SYSTEMS. 1984,17,180. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160393. GABRIEL WEATHERHEAD
  160394. 9205N
  160395. 2/28/96V
  160396. A REVIEW. SKELL, P. S., TRAYNHAM, J. G. RADICAL BROMINATIONS OF ALKYL BROMIDES AND THE NNTURE OF B BROMOALKYL RADICALS. 1984, 17, 160. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160397. GABRIEL WEATHERHEAD
  160398. 9206N
  160399. 2/28/96VnA REVIEW.  OKI, M. REACTIVITY OF CONFORMATIONAL ISOMERS. 1984,17, 154. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  160400. GABRIEL WEATHERHEAD
  160401. 9207N
  160402. 2/28/96V
  160403. A REVIEW. PAGE, M. I. THE MECHANISMS OF REACTIONS OF B LACTAM ANTIBIOTICS. 1984,17, 144. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160404. GABRIEL WEATHERHEAD
  160405. 9208N
  160406. 2/28/96V
  160407. A REVIEW. KROPP P. J. PHOTOBEHAVIOR OF ALKYL HALIDES IN SOLUTION: RADICAL, CARBOCATION, AND CARBENE INTERMEDIATES. 1984, 17, 131. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160408. GABRIEL WEATHERHEAD
  160409. 9209N
  160410. 2/28/96V
  160411. A REVIEW.  BARTOLI, G. CONJUGATE ADDITION OF ALKYL GRIGNARD REAGENTS TO MONONITROARENES. 1984,17,109 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160412. GABRIEL WEATHERHEAD
  160413. 9210N
  160414. 2/28/96V
  160415. A REVIEW. TSUJI, T.; NISHIDU, S. THERMAL RING OPENING CYCLOADDITIONS OF CYCLOPROPYL DERIVATIVES WITH ACTIVATED OLEFINS. 1984, 17, 56. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160416. GABRIEL WEATHERHEAD
  160417. 9211N
  160418. 2/28/96
  160419. A REVIEW. MAGNUS, P.; GALLAGHER, T.; BROWN, P.; PAPPALARDO, P. THE INDOLE 2,3 QUINODIMETHANE STRATEGY FOR THE SYNTHESIS OF INDOLE ALKALOIDS. 1984,17, 35. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160420. GABRIEL WEATHERHEAD
  160421. 9212N
  160422. 2/28/96VhA REVIEW. LIOTTA,D. NEW ORGANOSELENIUM METHODOLOGY. 1984,17, 28. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  160423. GABRIEL WEATHERHEAD
  160424. 9213N
  160425. 2/28/96V
  160426. A REVIEW.  1184a
  160427. GABRIEL WEATHERHEAD
  160428. 9214N
  160429. 2/28/96VjA REVIEW.  THAYER, J. S. ORGANOMETALLIC COMPOUNDS AND LIVING ORGANISMS. ACADEMIC PRESS: ORLANDO, FL, 1984.a
  160430. GABRIEL WEATHERHEAD
  160431. 9215N
  160432. 2/28/96VnA REVIEW. SPORN, M. B.; GOODMAN, D. S., EDS. THE RETINOIDS VOLUMES 1 AND 2. ACADEMIC PRESS: ORLANDO, FL, 1984.a
  160433. GABRIEL WEATHERHEAD
  160434. 9216N
  160435. 2/28/96VpA REVIEW. SCRIVEN, E. F. Y., ED. AZIDES AND NITRENES. REACTIVITY AND UTILITY. ACADEMIC PRESS: ORLANDO, FL, 1984.a
  160436. GABRIEL WEATHERHEAD
  160437. 9217N
  160438. 2/28/96V^A REVIEW. SCHUSTER, H. F., COPPOLA, G. M. ALLENES IN ORGANIC SYNTHESIS. WILEY: NEW YORK, 1984.a
  160439. GABRIEL WEATHERHEAD
  160440. 9218N
  160441. 2/28/96V
  160442. A REVIEW. RIDEOUT, J. L.; HENRY, D. W., BEACHAM, L. M., III, EDS. NUCLEOSIDES, NUCLEOTIDES, AND THEIR BIOLOGICAL APPLICATIONS. ACADEMIC PRESS: ORLANDO, FL, 1983.a
  160443. GABRIEL WEATHERHEAD
  160444. 9219N
  160445. 2/28/96VTA REVIEW. PADWA, A., ED. 1,3 DIPOLAR CYCLOADDITION CHEMISTRY. WILEY: NEW YORK, 1984.a
  160446. GABRIEL WEATHERHEAD
  160447. 9220N
  160448. 2/28/96ViA REVIEW. NUDELMAN, A, CHEMISTRY OF OPTICALLY ACTIVE SULFUR COMPOUNDS. GORDON AND BREACH: NEW YORK, 1984.a
  160449. GABRIEL WEATHERHEAD
  160450. 9221N
  160451. 2/28/96VqA REVIEW. NICOLAOU, K. C.; PETAISIS, N. A. SELENIUM IN NATURAL PRODUCTS SYNTHESIS. CIS, INC.: PHILADELPHIA, 1984.a
  160452. GABRIEL WEATHERHEAD
  160453. 9222N
  160454. 2/28/96V]A REVIEW. LLOYD, D. NON BENZENOID CONJUGATED CARBOCYCLIC COMPOUNDS. ELSEVIER: NEW YORK, 1984.a
  160455. GABRIEL WEATHERHEAD
  160456. 9223N
  160457. 2/28/96VqA REVIEW. LEDNICER, D.; MITSCHER, L. A. THE ORGANIC CHEMISTRY OF DRUG SYNTHESIS, VOLUME 3. WILEY: NEW YORK, 1984.a
  160458. GABRIEL WEATHERHEAD
  160459. 9224N
  160460. 2/28/96V\A REVIEW. HUDLICKY, M. REDUCTION IN ORGANIC CHEMISTRY. ELLIS HORWOOD LTD.: CHICHESTER, 1984.a
  160461. GABRIEL WEATHERHEAD
  160462. 9225N
  160463. 2/28/96VnA REVIEW. HARTLEY, F. R; PATAI, S.. EDS. THE NATURE AND CLEAVAGE OF METAL CARBON BONDS. WILEY: NEW YORK, 1985.a
  160464. GABRIEL WEATHERHEAD
  160465. 9226N
  160466. 2/28/96V^A REVIEW. GUPTA, R. R., ED. PHYSICAL METHODS IN HETEROCYCLIC CHEMISTRY. WILEY: NEW YORK, 1984.a
  160467. GABRIEL WEATHERHEAD
  160468. 9227N
  160469. 2/28/96V
  160470. A REVIEW. COLQUHOUN, H. M.; HOLTON, J.; THOMPSON, D. J.; TWIGG, M. V  NEW PATHWAYS FOR ORGANIC SYNTHESIS PRACTICAL APPLICATIONS OF TRANSITION METALS. PLENUM PRESS NEW YORK, 1984.a
  160471. GABRIEL WEATHERHEAD
  160472. 9228N
  160473. 2/28/96
  160474. A REVIEW. CHVALOVSKY, V.; BELLAMA, J. M., EDS. CARBON FUNCTIONAL ORGANOSILICON COMPOUNDS. PLENUM PRESS: NEW YORK AND LONDON, 1984.a
  160475. GABRIEL WEATHERHEAD
  160476. 9229N
  160477. 2/28/96VZA REVIEW.  BASSINDALE, A. THE THIRD DIMENSION IN ORGANIC CHEMLSTRY. WILEY: NEW YORK, 1984.a
  160478. GABRIEL WEATHERHEAD
  160479. 9230N
  160480. 2/28/96V
  160481. A REVIEW.  ATWOOD, J. L.; DAVIES, J. E. D. INCLUSION COMPOUNDS, VOLUME 3. PHYSICAL PROPERTIES AND APPLICATIONS. ACADEMIC PRESS: ORLANDO, FL, 1984.a
  160482. GABRIEL WEATHERHEAD
  160483. 9231N
  160484. 2/28/96V
  160485. A REVIEW. ATWOOD, J. L.; DAVIES, J. E. D. INCLUHION COMPOUNDS VOLUME 2. STRUCTURAL ASPECTS OF INCLUSION COMPOUNDS FORMED BY ORGANIC HOST LATTICES. ACADEMIC PRESS: ORIANDO, FL, 1984.a
  160486. GABRIEL WEATHERHEAD
  160487. 9232N
  160488. 2/28/96V
  160489. A REVIEW.  ATWOOD, J. L.; DAVIES J. E. D. INCLUSION COMPOUNDS, VOLUME 1. STRUCTURAI ASPECTS OF INCLUSION COMPOUNDS FORMED BY INORGANIC AND ORGANOMETALLIC HOST LATTICES. ACADEMIC PRESS: ORLANDO, FL, 1984.
  160490. GABRIEL WEATHERHEAD
  160491. 9233N
  160492. 2/28/96VcA REVIEW. APSIMON J., ED. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOLUME 6. WILEY: NEW YORK, 1984.a
  160493. GABRIEL WEATHERHEAD
  160494. 9234N
  160495. 2/28/96V
  160496. A REVIEW.  FISCHER, H. MECHANISTIC ASPECTS OF CARBENE COMPLEXES REACTIONS. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160497. GABRIEL WEATHERHEAD
  160498. 9235N
  160499. 2/28/96V
  160500. A REVIEW. WEISS, K. CARBENE COMPLEXES AS INTERMEDIATES IN CATALYTIC REACTIONS. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160501. GABRIEL WEATHERHEAD
  160502. 9236N
  160503. 2/28/96V
  160504. A REVIEW. DOTZ, K. H. CARBENE COMPLEXES IN ORGANIC SYNTHESIS. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160505. GABRIEL WEATHERHEAD
  160506. 9237N
  160507. 2/28/96
  160508. A REVIEW.  KREISSL, F. R. METAL COMPLEXES FROM CARBENE COMPLEXES: SELECTED REACTIONS. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160509. GABRIEL WEATHERHEAD
  160510. 9238N
  160511. 2/28/96V
  160512. A REVIEW. HOFMANN, P. ELECTRONIC STRUCTURES OF TRANSITION METAL CARBENE COMPLEXES TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160513. GABRIEL WEATHERHEAD
  160514. 9239N
  160515. 2/28/96V
  160516. A REVIEW. SCHUBERT, U. SOLID STATE STRUCTURES OF CARBENE COMPLEXES. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160517. GABRIEL WEATHERHEAD
  160518. 9240N
  160519. 2/28/96V
  160520. A REVIEW. FISCHER, H.; KREISSL, F. R. SPECTROSCOPIC PROPERTIES OF TRANSITION METAL CARBENE COMPLEXES. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160521. GABRIEL WEATHERHEAD
  160522. 9241N
  160523. 2/28/96
  160524. A REVIEW.  FISCHER, H. THE SYNTHESIS OF CARBENE COMPLEXES. TRANSITION METAL COMPLEXES, VERLAG CHEMIE INTERNATIONAI: DEERFIELD BEACH, FL, 1983.a
  160525. GABRIEL WEATHERHEAD
  160526. 9242N
  160527. 2/28/96V
  160528. A REVIEW.  PETERSON, W. R.; ANDERSON, R. SILANE BLOCKING AGENTS, P 60. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160529. GABRIEL WEATHERHEAD
  160530. 9243N
  160531. 2/28/96V
  160532. A REVIEW.  MULLER, R ORGANOFLUOROSILICATE CHEMISTRY, P 60. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160533. GABRIEL WEATHERHEAD
  160534. 9244N
  160535. 2/28/96V~A REVIEW. WEST, R. ORGANOPOLYSILANES, P 41. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160536. GABRIEL WEATHERHEAD
  160537. 9245N
  160538. 2/28/96V
  160539. A REVIEW. BROOK, A. G. SILENE CHEMISTRY, P 33. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160540. GABRIEL WEATHERHEAD
  160541. 2/28/96V
  160542. A REVIEW.  LARSON, C. L. A SILYL CARBONYL COMPOUNDS SYNTHESIS AND REACTIONS, P 22. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160543. GABRIEL WEATHERHEAD
  160544. 9247N
  160545. 2/28/96V
  160546. A REVIEW.  CUNICO, R F. SYNTHETIC ASPECTS OF ACYLSILANE CHEMISTRY, P 15. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS, INC.: BRISTOL, PA, 1984.a
  160547. GABRIEL WEATHERHEAD
  160548. 9248N
  160549. 2/28/96V
  160550. A REVIEW. CASPAR, P. SILYLENES, P 333. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160551. GABRIEL WEATHERHEAD
  160552. 9249N
  160553. 2/28/96V
  160554. A REVIEW. LWOWSKI, W. NITRENES, P 306. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160555. GABRIEL WEATHERHEAD
  160556. 9250N
  160557. 2/28/96
  160558. A REVIEW. KAPLAN, L. FREE RADICALS, P 227. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160559. GABRIEL WEATHERHEAD
  160560. 9251N
  160561. 2/28/96V
  160562. A REVIEW.  ARNETT, E. M.; HOFELICH, T. C.; SCHRIVER, C. W. CARBOCATIONS, P 189. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160563. GABRIEL WEATHERHEAD
  160564. 9252N
  160565. 2/28/96V
  160566. A REVIEW. BORDEN, W. T. DIRADICALS, P 161. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160567. GABRIEL WEATHERHEAD
  160568. 9253N
  160569. 2/28/96V
  160570. A REVIEW. CASEY, C. P. METAL CARBENE COMPLEXES, P. 109. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160571. GABRIEL WEATHERHEAD
  160572. 9254N
  160573. 2/28/96
  160574. A REVIEW.  MOSS, R. A., JONES, M., JR. CARBENES, P 46. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160575. GABRIEL WEATHERHEAD
  160576. 9255N
  160577. 2/28/96V
  160578. A REVIEW.  STALEY, S. W. CARBANIONS, P 19. REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160579. GABRIEL WEATHERHEAD
  160580. 9256N
  160581. 2/28/96V
  160582. A REVIEW.  LEVIN, R H. ARYNES, P 1 REACTIVE INTERMEDIATES, VOLUME 3, M. JONES, JR. AND R. A. MOSS, EDS., WILEY LNTERSCIENCE: NEW YORK. 1984,a
  160583. GABRIEL WEATHERHEAD
  160584. 9257N
  160585. 2/28/96
  160586. A REVIEW. SIMS, L. B.; LEWIS, D. E. BOND ORDER METHODS FOR CALCULATING ISOTOPE EFFECTS IN ORGANIC REACTIONS. ISOTOPES IN ORGANIC CHEMISTRY, VOLUME 6. ISOTOPIC EFFECTS: RECENT DEVELOPMENTS IN THEORY AND EXPERIMENT, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1984.
  160587. GABRIEL WEATHERHEAD
  160588. 9258N
  160589. 2/28/96
  160590. A REVIEW. TURRO, N. J.; KRAEUTLER, B. MAGNETIC ISOTOPE EFFECTS. ISOTOPES IN ORGANIC CHEMISTRY, VOLUME 6. ISOTOPIC EFFECTS: RECENT DEVELOPMENTS IN THEORY AND EXPERIMENT, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1984.a
  160591. GABRIEL WEATHERHEAD
  160592. 9259N
  160593. 2/28/96V
  160594. A REVIEW. ISAACS, N. S. THE EFFECTS OF PRESSURE ON KINETIC ISOTOPE EFFECTS. ISOTOPES IN ORGANIC CHEMISTRY, VOLUME 6. ISOTOPIC EFFECTS: RECENT DEVELOPMENTS IN THEORY AND EXPERIMENT, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1984.a
  160595. GABRIEL WEATHERHEAD
  160596. 9260N
  160597. 2/28/96V
  160598. A REVIEW.  FORSYTH, D. A. ISOTOPE EFFECTS ON 13C NMR SHIFTS AND COUPLING CONSTANTS. ISOTOPES IN ORGANIC CHEMISTRY, VOLUME 6. ISOTOPIC EFFECTS: RECENT DEVELOPMENTS IN THEORY AND EXPERIMENT, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1984.a
  160599. GABRIEL WEATHERHEAD
  160600. 9261N
  160601. 2/28/96
  160602. +A REVIEW.  MARYANOFF, C. A., MARYANOFF, B. E. SYNTHESIS AND UTILIZATION OF COMPOUNDS WITH CHIRAL SILICON CENTERS. ASYMMETRIC SYNTHESIS, VOLUME 4. THE CHIRAL CARBON POOL AND CHIRAL SULFUR, NITROGEN PHOSPHORUS, AND SILICON CENTERS, J. D. MORRISON AND J. W. SCOTT, EDS., ACADEMIC PRESS: NEW YORK, 1984.
  160603. GABRIEL WEATHERHEAD
  160604. 9262N
  160605. 2/28/96
  160606. *A REVIEW. DAVIS, F. A.; JENKINS, R. H., JR. SYNTHESIS AND UTILIZATION OF COMPOUNDS WITH CHIRAL NITROGEN CENTERS. ASYMMETRIC SYNTHESIS, VOLUME 4. THE CHIRAL CARBON POOL AND CHIRAL SULFUR, NITROGEN PHOSPHORUS, AND SILICON CENTERS, J. D. MORRISON AND J. W. SCOTT, EDS., ACADEMIC PRESS: NEW YORK, 1984.
  160607. GABRIEL WEATHERHEAD
  160608. 9263N
  160609. 2/28/96
  160610. (A REVIEW. VALENTINE, D., JR. PREPARATION OF THE ENANTIOMERS OF COMPOUNDS CONTAINING CHIRAL PHOSPHORUS CENTERS. ASYMMETRIC SYNTHESIS, VOLUME 4. THE CHIRAL CARBON POOL AND CHIRAL SULFUR, NITROGEN PHOSPHORUS, AND SILICON CENTERS, J. D. MORRISON AND J. W. SCOTT, EDS., ACADEMIC PRESS: NEW YORK, 1984.
  160611. GABRIEL WEATHERHEAD
  160612. 9264N
  160613. 2/28/96
  160614. 6A REVIEW. JOHNSON, C. R.; BARBACHYN, M. R. OPTICAL ACTIVATION AND UTILIZATION OF COMPOUNDS CONTAINING CHIRAL SULFUR CENTERS. ASYMMETRIC SYNTHESIS, VOLUME 4. THE CHIRAL CARBON POOL AND CHIRAL SULFUR, NITROGEN PHOSPHORUS, AND SILICON CENTERS, J. D. MORRISON AND J. W. SCOTT, EDS., ACADEMIC PRESS: NEW YORK, 1984.
  160615. GABRIEL WEATHERHEAD
  160616. 9265N
  160617. 2/28/96
  160618. A REVIEW.  SCOTT, J. W. READILY AVAILABLE CHIRAL CARBON FRAGMENTS AND THEIR USE IN SYNTHESIS. ASYMMETRIC SYNTHESIS, VOLUME 4. THE CHIRAL CARBON POOL AND CHIRAL SULFUR, NITROGEN PHOSPHORUS, AND SILICON CENTERS, J. D. MORRISON AND J. W. SCOTT, EDS., ACADEMIC PRESS: NEW YORK, 1984.
  160619. GABRIEL WEATHERHEAD
  160620. 9266N
  160621. 2/28/96V
  160622. A REVIEW. WANG, P.; JOULLIE, M. MUSCARINE ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160623. GABRIEL WEATHERHEAD
  160624. 9267N
  160625. 2/28/96V
  160626. A REVIEW.  BUCK, K. T. AZAFLUORANTHENE AND TROPOLOISOQUINOLINE ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160627. GABRIEL WEATHERHEAD
  160628. 9268N
  160629. 2/28/96
  160630. A REVIEW.  SUZUKI, T., IWAI, K. CONSTITUENTS OF RED PEPPER SPECIES: PUNGENT PRINCIPLE OF CAPSICUM SPECIES. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160631. GABRIEL WEATHERHEAD
  160632. 9269N
  160633. 2/28/96V
  160634. A REVIEW.  HUANG, L.; XUE, Z. CEPHALOTASUS ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160635. GABRIEL WEATHERHEAD
  160636. 9270N
  160637. 2/28/96V
  160638. A REVIEW.  REIDER, P. J., ROLAND, D. M. MAYTANSINOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160639. GABRIEL WEATHERHEAD
  160640. 9271N
  160641. 2/28/96V
  160642. A REVIEW.  CAPRARO, H., BROSSI, A. TROPOLONIC COLCHICUM ALKALOIDS. THE ALKALOIDS, CHEMISTRY AND PHARMACOLOGY, VOLUME 23, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1984.a
  160643. GABRIEL WEATHERHEAD
  160644. 9272N
  160645. 2/28/96
  160646. VSA REVIEW. GUTSCHE, C. D. THE CALIXARENES. 1984, 123, 1. TOPICS IN CURRENT CHEMISTRYa
  160647. GABRIEL WEATHERHEAD
  160648. 9273N
  160649. 2/28/96V
  160650. A REVIEW. KOPTYUG, V. A. CONTEMPORARY PROBLEMS IN CARBONIUM ION CHEMISTRY III. ARENIUM IONS  STRUCTURE SND REACTIVITY. 1984, 122, 1. TOPICS IN CURRENT CHEMISTRYa
  160651. GABRIEL WEATHERHEAD
  160652. 9274N
  160653. 2/28/96V
  160654. A REVIEW.  LIPSHUTZ, B. H.; WILHELM, R. S.; KOZLOWSKI, J. A. THE CHEMISTRY OF HIGHER ORDER ORGANOCUPRATES. 1984, 40, 5005. TETRAHEDRONa
  160655. GABRIEL WEATHERHEAD
  160656. 9275N
  160657. 2/28/96VsA REVIEW. SHAMMA, M.; GUINAUDEAU, H. BIOGENETIC PATHWAYS FOR THE APORPHINOID ALKALOIDS. 1984, 40, 4795. TETRAHEDRONa
  160658. GABRIEL WEATHERHEAD
  160659. 9276N
  160660. 2/28/96VqA REVIEW. PAGNI, R. M. MULTIPLY CHARGED CARBOCATIONS AND RELATED SPECIES IN SOLUTION. 1984, 40, 4161. TETRAHEDRONa
  160661. GABRIEL WEATHERHEAD
  160662. 9277N
  160663. 2/28/96
  160664. VcA REVIEW.  MICHL, J. MAGNETIC CIRCULAR DICHROISM OF AROMATIC MOLECULES. 1984, 40, 3845. TETRAHEDRONa
  160665. GABRIEL WEATHERHEAD
  160666. 9278N
  160667. 2/28/96VhA REVIEW.  SANTHANAKRISHNAN, T. S. BIOHYDROXLYLATION OF TERPENES IN MAMMALS. 1984, 40, 3697. TETRAHEDRONa
  160668. GABRIEL WEATHERHEAD
  160669. 9279N
  160670. 2/28/96V
  160671. A REVIEW. RABAN, M.; KOST, D. STEREOLABILE CONFIGURATIONAL UNITS. TORSIONAL AND INVERSIONAL STEREOCHEMISTRY IN SULFENAMIDES AND HYDROXYLAMINES. 1984, 40, 3345. TETRAHEDRONa
  160672. GABRIEL WEATHERHEAD
  160673. 9280N
  160674. 2/28/96V
  160675. A REVIEW.  INCH, T. D. FORMATION OF CONVENIENT CHIRAL INTERMEDIATES FROM CARBOHYDRATES AND THEIR USE IN SYNTHESIS. 1984, 40, 3161. TETRAHEDRONa
  160676. GABRIEL WEATHERHEAD
  160677. 9281N
  160678. 2/28/96VoA REVIEW.  HICKMOTT, P. W. RECENT ADVANCES IN THE CHEMISTRY OF CONJUGATED ENAMINES. 1984, 40, 2989. TETRAHEDRONa
  160679. GABRIEL WEATHERHEAD
  160680. 9282N
  160681. 2/28/96
  160682. V\A REVIEW.  PASTO, D. J. RECENT DEVELOPMENTS IN ALLENE CHEMISTRY. 1984, 40, 2806. TETRAHEDRONa
  160683. GABRIEL WEATHERHEAD
  160684. 9283N
  160685. 2/28/96VpA REVIEW. DELUCCHI, O., MODENA, G. ACETYLENE EQUIVALENTS IN CYCLOADDITION REACTIONS. 1984, 40, 2686. TETRAHEDRONa
  160686. GABRIEL WEATHERHEAD
  160687. 9284N
  160688. 2/28/96VfA REVIEW.  HEGEDUS, L. S. PALLADIUM(II) ASSISTED REACTIONS OF MONOOLEFINS. 1984, 40, 2416. TETRAHEDRONa
  160689. GABRIEL WEATHERHEAD
  160690. 9285N
  160691. 2/28/96V`A REVIEW.  YOKOYAMA, M.; IMAMOTO, T. ORGANIC REACTIONS OF CARBON DISULFIDE. 1984, 797. SYNTHESISa
  160692. GABRIEL WEATHERHEAD
  160693. 9286N
  160694. 2/28/96V^A REVIEW. VARVOGLIS, A. POLYVALENT LODINE COMPOUNDS IN ORGANIC SYNTHESIS. 1984, 709. SYNTHESISa
  160695. GABRIEL WEATHERHEAD
  160696. 9287N
  160697. 2/28/96VXA REVIEW.  SMITH, J. G. SYNTHETICALLY USEFUL REACTIONS OF EPOXIDES. 1984, 629. SYNTHESISa
  160698. GABRIEL WEATHERHEAD
  160699. 9288N
  160700. 2/28/96
  160701. V_A REVIEW.  RAMAIAH, M. CYCLOPENTANNELLTION REACTIONS IN ORGANIC SYNTHESIS. 1984, 529. SYNTHESISa
  160702. GABRIEL WEATHERHEAD
  160703. 9289N
  160704. 2/28/96V
  160705. A REVIEW. KARAEV, S. F.; GORAEVA, SH. V.; SLADKOV, A. M. PROPARGYL COMPOUNDS IN THE SYNTHESIS OF CARBOCYCLES SND HETEROCYCLES. 1984, 53, 492. RUSSIAN CHEMICAL REVIEWSa
  160706. GABRIEL WEATHERHEAD
  160707. 9290N
  160708. 2/28/96V
  160709. A REVIEW. EGOROCHKIN, A. N. THE SPECTROSCOPY OF ORGANIC COMPOUNDS OF SILICON SUBGROUP ELEMENTS AND HYPERCONJUGATION. 1984, 53, 446. RUSSIAN CHEMICAL REVIEWSa
  160710. GABRIEL WEATHERHEAD
  160711. 9291N
  160712. 2/28/96V
  160713. A REVIEW. DOMBROVSKII V. A; FONSKII. D. YU; MIRONOV, V. S THE SYNTHSIS OF PROSTAGLANDINS FROM CYCLOPENTANE DERIVATIVES 1984, 53, 401. RUSSIAN CHEMICAL REVIEWSa
  160714. GABRIEL WEATHERHEAD
  160715. 9292N
  160716. 2/28/96VeA REVIEW. GRANIK, V. C. ADVANCES IN THE CHEMISTRY OF ENAMINES. 1984, 53, 369 RUSSIAN CHEMICAL REVIEWSa
  160717. GABRIEL WEATHERHEAD
  160718. 9293N
  160719. 2/28/96
  160720. A REVIEW. ERASTOV, O. A.; NIKONOV, G. N. TERTIARY PHOSPHINES WITH FUNCTIONAL GROUP SUBSTITUENTS 1984, 53, 369. RUSSIAN CHEMICAL REVIEWSa
  160721. GABRIEL WEATHERHEAD
  160722. 9294N
  160723. 2/28/96VxA REVIEW. MERKUHHEV, E. V. ADVANCES IN THE SYNTHESIS OF AROMATIC IODO COMPOUNDS. 1984, 53, 343. RUSSIAN CHEMICAL REVIEWSa
  160724. GABRIEL WEATHERHEAD
  160725. 9295N
  160726. 2/28/96V
  160727. A REVIEW. SAMUILOV, YA. D.; KONOVALOV, A. I. THE REACTIVITY OF ADDENDS IN THE 1,3 DIPOLAR CYCLOADDITION REACTION. 1984, 53, 332. RUSSIAN CHEMICAL REVIEWSa
  160728. GABRIEL WEATHERHEAD
  160729. 9296N
  160730. 2/28/96V
  160731. A REVIEW.  REUTOV, O. A. SOME REARRANGEMENTS OF FREE ALKYL RADICALS AND ALKYL CATIONS IN SOLUTIONS. 1984, 53, 274. RUSSIAN CHEMICAL REVIEWSa
  160732. GABRIEL WEATHERHEAD
  160733. 9297N
  160734. 2/28/96V
  160735. A REVIEW.  ZEIFMAN, YU. V.; TER GABRIELYAN, E. G.; GAMIBARYAN, N. P.; KNUNYANTS, I. L. THE CHEMISTRY OF PERFLUOROISOBUTENE. 1984, 53, 256. RUSSIAN CHEMICAL REVIEWSa
  160736. GABRIEL WEATHERHEAD
  160737. 9298N
  160738. 2/28/96V}A REVIEW. FOKIN, A. V.; KOLOMIETS, A. F.; VASIL'EV, N. V. FLUORINE CONTAINING IMINES. 1984, 53, 238. RUSSIAN CHEMICAL REVIEWSa
  160739. GABRIEL WEATHERHEAD
  160740. 9299N
  160741. 2/28/96V
  160742. A REVIEW.  DOLGOPLOSK, B. A.; KORSHAK, YU. V. ORGANOMETALLIC CATSLYSIS IN DIENE AND CYCLO OLEFIN POLYMERIZATION PROCESSES. II. THE METATHESIS REACTION IN POLYMER CHEMISTRY. 1984, 53, 36. RUSSIAN CHEMICAL REVIEWSa
  160743. GABRIEL WEATHERHEAD
  160744. 9300N
  160745. 2/28/96V
  160746. A REVIEW. DOLGOPLOSK, B. A.; TINYAKOVA, E. 1. ORGANOMETALLIC CATSLYSIS IN DIENE AND CYCLO OLEFIN POLYMERIZATION PROCESSES. I. 1984, 53, 22. RUSSIAN CHEMICAL REVIEWSa
  160747. GABRIEL WEATHERHEAD
  160748. 9301N
  160749. 2/28/96VwA REVIEW. SHIMIZU, Y. PARALYTIC SHELLFISH POISONS. 1984, 45, 236. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160750. GABRIEL WEATHERHEAD
  160751. 9302N
  160752. 2/28/96
  160753. A REVIEW. ELIZ, I. A.; WHITTON, A. A.; SARGENT, M. V. RECENT PROGRESS IN THE CHEMISTRY OF LICHEN SUBSTANCES. 1984, 45, 103. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160754. GABRIEL WEATHERHEAD
  160755. 9303N
  160756. 2/28/96V
  160757. A REVIEW.  TAYLOR, D. A. H. THE CHEMISTRY OF THE LIMONOIDS FROM MELIACEAE. 1984, 45, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  160758. GABRIEL WEATHERHEAD
  160759. 9304N
  160760. 2/28/96V
  160761. A REVIEW. HUDLICKY, T., KUTCHAN, T. M.; NAQVI, S. M. THE VINYLCYCLOPROPANE CYCLOPENTENE REARRANGEMENT. 1985, 33, 247. ORGANIC REACTIONSa
  160762. GABRIEL WEATHERHEAD
  160763. 9305N
  160764. 2/28/96V
  160765. A REVIEW. NEGISHI, E. I., IDACAVAGE, M. J. FORMATION OF CARBON CARBON AND CARBON HETEROATOM BONDS VIA ORGANOBORANES AND ORGANOBORATES. 1985, 33, 1. ORGANIC REACTIONSa
  160766. GABRIEL WEATHERHEAD
  160767. 9306N
  160768. 2/28/96
  160769. A REVIEW. ZWEIFEL, G.; MILLER, J. A. SYNTHESIS USING ALKYNE DERIVED ALKENYL  AND ALKYNYLALUMINUM COMPOUNDS. 1984, 32. ORGANIC REACTIONSa
  160770. GABRIEL WEATHERHEAD
  160771. 9307N
  160772. 2/28/96VZA REVIEW. CIGANEK, E. THE INTRAMOLECULAR DIELS ALDER REACTION. 1984, 32. ORGANIC REACTIONSa
  160773. GABRIEL WEATHERHEAD
  160774. 9308N
  160775. 2/28/96V
  160776. A REVIEW.  HUTCHINS, R O., LEANR, K., NAZER B.; PYTLEWSKI, D. PELTER A. AMINE BORANES AS SELECTIVE; REDUCING AND HYDROBORATING AGENTS. 1984, 16, 335. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160777. GABRIEL WEATHERHEAD
  160778. 9309N
  160779. 2/28/96V
  160780. A REVIEW. HEARN, M. J.; LEVY, F. RECENT PROGRESS IN THE SYNTHESIS AND REACTIONS OF 1,2,3  AND 1,2,4 TRIAZINES. 1984,16,199. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160781. GABRIEL WEATHERHEAD
  160782. 9310N
  160783. 2/28/96
  160784. A REVIEW. MILLS, J. E.; MARYANOFF, C. A.; COSGROVE. R. M.; SCOTT, L; MCCOMSEY, D. F. THE REACTION OF AMINES WITH METHYLENE CHLORIDE. 1984, 16, 97. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160785. GABRIEL WEATHERHEAD
  160786. 9311N
  160787. 2/28/96V
  160788. A REVIEW. MCDERMOTT, S. D., SPILLANE, W. J. SYNTHESIS AND REACTIONS IN SULFAMIDES. 1984, 16. 49. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160789. GABRIEL WEATHERHEAD
  160790. 9312N
  160791. 2/28/96VyA REVIEW. NATALE, N. R. LANTHANIDES IN ORGANIC SYNTHESIS 1983, 15, 387. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160792. GABRIEL WEATHERHEAD
  160793. 9313N
  160794. 2/28/96V
  160795. A REVIEW.  PINNICK, H. W. POTASSIUM HYDRIDE IN ORGANIC SYNTHESIS. 1983, 15, 199. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  160796. GABRIEL WEATHERHEAD
  160797. 9314N
  160798. 2/28/96V
  160799. A REVIEW. OAE, S.; SHINHAMA, K. ORGANIC THIONITRITES AND RELATED SUBSTANCES. 1983,15, 165. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL
  160800. GABRIEL WEATHERHEAD
  160801. 9315N
  160802. 2/28/96VwA REVIEW. LABIA, R.; MORIN, C. STEREOSPECIFIC CONSTRUCTIONS OF CHIRAL B LACTAMS. 1984, 37, 1103. JOURNAL OF ANTIBIOTICSa
  160803. GABRIEL WEATHERHEAD
  160804. 9316N
  160805. 2/28/96VrA REVIEW.  MARKGRAF, J. H. INFRARED CARBONYL FREQUENCIES OF THIOLACTONES AND LACTONES 1984, 22, 2601. HETEROCYCLESa
  160806. GABRIEL WEATHERHEAD
  160807. 9317N
  160808. 2/28/96V
  160809. A REVIEW. FIFE, W. K.; SCRIVEN, E. R. CYANATION IN THE PYRIDINE SERIES: SYNTHETIC APPLICATIONS OF THE REISSERT HENZE AND RELATED REACTIONS. 1984, 22, 2375. HETEROCYCLESa
  160810. GABRIEL WEATHERHEAD
  160811. 9318N
  160812. 2/28/96VoA REVIEW. SURPATEANU, G., LABLACHE COMBIER, A. REACTIVITY OF CYCLOIMMONIUM YLIDES. 1984, 22, 2079. HETEROCYCLESa
  160813. GABRIEL WEATHERHEAD
  160814. 9319N
  160815. 2/28/96V
  160816. A REVIEW. HAFEZ. E. A. A.; ABED, N. M.; ELMOGHAYER, M. R. H.; EL AGAMEY, A. G. A.  HYDRAZINES AND HYDRAZINE DERIVATIVES IN HETEROCYCLIC SYNTHESIS. 1984, 22,1821. HETEROCYCLES
  160817. GABRIEL WEATHERHEAD
  160818. 9320N
  160819. 2/28/96VzA REVIEW. LOUNASMAN, M. KOSKINEN, A. MODIFIED POLONOVSKI REACTION, A VERSATILE SYNTHETIC TOOL. 1984, 22,1591. HETEROCYCLESa
  160820. GABRIEL WEATHERHEAD
  160821. 9321N
  160822. 2/28/96VJA REVIEW. SLIWA, W. THE CHEMISTRY OF FURAZANS. 1984, 22,1571. HETEROCYCLESa
  160823. GABRIEL WEATHERHEAD
  160824. 9322N
  160825. 2/28/96VuA REVIEW.  ATTYGALLE, A. B.; MORGAN, E. D. CHEMICALS FROM THE GLANDS OF ANTS. 1984, 13, 245. CHEMICAL SOCIETY REVIEWSa
  160826. GABRIEL WEATHERHEAD
  160827. 9323N
  160828. 2/28/96VZA REVIEW. MULLEN, K. REDUCTION AND OXIDATION OF ANNULENES. 1984, 84, 603. CHEMICAL REVIEWSa
  160829. GABRIEL WEATHERHEAD
  160830. 9324N
  160831. 2/28/96VuA REVIEW. BERGERON, R. J. SYNTHESIS AND SOLUTION STRUCTURE OF MICROBIAL SIDEROPHORES. 1984, 84, 587. CHEMICAL REVIEWSa
  160832. GABRIEL WEATHERHEAD
  160833. 9325N
  160834. 2/28/96VcA REVIEW. ZOELLNER, R. W.; KLABUNDE. K. J. ALKYNES AND METAL ATOMS. 1984, 84, 545. CHEMICAL REVIEWS
  160835. GABRIEL WEATHERHEAD
  160836. 9326N
  160837. 2/28/96V
  160838. A REVIEW. KANE MAGUIRE, L. A. P.; HONIG, E. D.; SWEIGART, D. A. NUCLEOPHILIC ADDITION TO COORDINATED CYCLIC P HYDROCARBONS: MECHANISTIC AND SYNTHETIC STUDIES. 1984, 84, 525. CHEMICAL REVIEWSa
  160839. GABRIEL WEATHERHEAD
  160840. 9327N
  160841. 2/28/96V
  160842. A REVIEW.  BEAK, P.; ZAJDEL, W. J.; REITZ, D. B. METALATION AND ELECTROPHILIC SUBSTITUTION OF AMINE DERIVATIVES ADJACENT TO NITROGEN A METALLO AMINE SYNTHETIC EQUIVALENTS. 1984, 84, 471 CHEMICAL REVIEWSa
  160843. GABRIEL WEATHERHEAD
  160844. 9328N
  160845. 2/28/96VYA REVIEW. STOWELL, J. C. THREE CARBON HOMOLOGATING AGENTS. 1984 84, 409. CHEMICAL REVIEWSa
  160846. GABRIEL WEATHERHEAD
  160847. 9329N
  160848. 2/28/96V
  160849. A REVIEW.  BLANEY, J. M. STRUCTURE ACTIVITY RELATIONSHIPS OF DIHYDROFOLATE REDUCTASE INHIBITORS 1984, 84, 333. CHEMICAL REVIEWSa
  160850. GABRIEL WEATHERHEAD
  160851. 9330N
  160852. 2/28/96
  160853. VjA REVIEW.  SCHON, I. SODIUM LIQUID AMMONIA REDUCTION IN PEPTIDE CHEMISTRY. 1984, 84, 287. CHEMICAL REVIEWSa
  160854. GABRIEL WEATHERHEAD
  160855. 9331N
  160856. 2/28/96V`A REVIEW.  TODY, S. CHEMILUMINESCENCE IN THE REACTIONS OF OZONE. 1984, 84, 277. CHEMICAL REVIEWSa
  160857. GABRIEL WEATHERHEAD
  160858. 9332N
  160859. 2/28/96V
  160860. A REVIEW. BUTLER, R. N. COMPARATIVE REACTIONS OF NITROGEN COMPOUNDS WITH THE ISOELECTRONIC SERIES MERCURY(II), THALLIUM(III), AND LEAD(IV) ACETATES. PRINCIPLES OF OXIDATION REACTIONS. 1984, 84, 249. CHEMICAL REVIEWSa
  160861. GABRIEL WEATHERHEAD
  160862. 9333N
  160863. 2/28/96VgA REVIEW. LUTZ, R. P. CATALYSIS OF THE COPE AND CLAISEN REARRANGEMENTS. 1984, 84, 205. CHEMICAL REVIEWSa
  160864. GABRIEL WEATHERHEAD
  160865. 9334N
  160866. 2/28/96V
  160867. A REVIEW.  OPPOLZER, W. ASYMMETRIC DIELS ALDER AND ENE REACTIONS IN ORGANIC SYNTHESIS. 1984, 23, 876. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160868. GABRIEL WEATHERHEAD
  160869. 9335N
  160870. 2/28/96
  160871. A REVIEW.  NOYORI, R; SUZUKI, M. PROSTAGLANDIN SYNTHESIS BY THREE COMPONENT COUPLING. 1984, 23, 847. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160872. GABRIEL WEATHERHEAD
  160873. 9336N
  160874. 2/28/96V
  160875. A REVIEW.  KELLOGG, R M.  CHIRAL MACROCYCLES AS REAGENTS AND CATALYSTS     1984, 23, 782 ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160876. GABRIEL WEATHERHEAD
  160877. 9337N
  160878. 2/28/96V
  160879. A REVIEW. ALT, H. G. PHOTOCHEMISTRY OF ALKYLTRANSITION METAL COMPLEXES 1984, 23, 766 ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160880. GABRIEL WEATHERHEAD
  160881. 9338N
  160882. 2/28/96V
  160883. A REVIEW. SCHURIG, V. GAS CHROMATOGRAPHIC SEPARATION OF ENANTIOMERS ON METAL COMPLEX FREE STATIONARY PHASES. 1984, 23, 747. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160884. GABRIEL WEATHERHEAD
  160885. 9339N
  160886. 2/28/96
  160887. A REVIEW. WILLIAMS, D. J. ORGANIC POLYMERIC AND NON POLYMERIC MATERIALS WITH LARGE OPTICAL NON LINEARITIES 1984, 23, 690 ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160888. GABRIEL WEATHERHEAD
  160889. 9340N
  160890. 2/28/96V
  160891. A REVIEW.  DOTZ, K. H. CARBENE COMPLEXES IN ORGANIC SYNTHESIS. 1984, 23, 687. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160892. GABRIEL WEATHERHEAD
  160893. 9341N
  160894. 2/28/96V
  160895. A REVIEW. OVERMAN, L. E. MERCURY(II)  AND PALLADIUM(II) CATALYZED [3.3]SIGMATROPIC REARRANGEMENTS. 1984, 23, 679. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160896. GABRIEL WEATHERHEAD
  160897. 9342N
  160898. 2/28/96V
  160899. A REVIEW. SIH, C. J.; CHEN, C. S. MICROBIAL ASYMMETRIC CATALYSIS
  160900. ENANTIOSELECTIVE REDUCTION OF KETONES. 1984, 23, 670. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160901. GABRIEL WEATHERHEAD
  160902. 9343N
  160903. 2/28/96
  160904. A REVIEW. REETZ, M. T. CHELALION OR NON CHELATION CONTROL IN ADDITION REACTIONS OF CHLRAL A  AND B AIKOXY CARBONYL COMPOUNDS. 1984, 23, 556. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160905. GABRIEL WEATHERHEAD
  160906. 9344N
  160907. 2/28/96V
  160908. A REVIEW. VOLLHARDT, K. P. C. COBALT MEDIATED [2 + 2 + 2] CYCLOADDITIONS: A MATURING SYNTHETIC STRATEGY. 1984, 23. 539. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160909. GABRIEL WEATHERHEAD
  160910. 9345N
  160911. 2/28/96V
  160912. A REVIEW. FRANCK B. MYCOTOXINS FROM MOLD FUNGI: STRUCTURES BIOLOGICAL ACTIVITY, BIOSYNTHESIS, AND PRECAUTIONS. 1984, 23, 493. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160913. GABRIEL WEATHERHEAD
  160914. 9346N
  160915. 2/28/96VsA REVIEW. SCHUMANN, H. ORGANOLANTHANOID COMPOUNDS. 1984, 23, 474. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160916. GABRIEL WEATHERHEAD
  160917. 9347N
  160918. 2/28/96
  160919. A REVIEW.  KATRITZKY, A. R., MARSON, C. M. PYRILIUM MEDIATED TRANSFORMATIONS OF PRIMARY AMINE GROUPS INTO OTHER FUNCTIONAL GROUPS. 1984, 23, 420. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160920. GABRIEL WEATHERHEAD
  160921. 9348N
  160922. 2/28/96V
  160923. A REVIEW. GIORDANO, C.; CASTALDI, G.; UGGERI, F. SYNTHESIS OF ANTI INFLAMMATORY A ARYLALKANOIC ACIDS BY 1 2 ARYL SHIFT. 1984, 23, 413. ANGEWANTE CHEMIE INTERNATIONAL EDITION IN ENGLISHa
  160924. GABRIEL WEATHERHEAD
  160925. 9349N
  160926. 2/28/96VZA REVIEW. BRISTOW, C. S. TIN REAGENTS FOR ORGANIC SYNTHESIS. 1984, 17,75 ALDRICHIMICA ACTAa
  160927. GABRIEL WEATHERHEAD
  160928. 9350N
  160929. 2/28/96ViA REVIEW.  DESONGCHAMPS, P. THE CONCEPT OF STRATEGY IN ORGANIC SYNTHESIS. 1984, 17, 69. ALDRICHIMICA ACTAa
  160930. GABRIEL WEATHERHEAD
  160931. 9351N
  160932. 2/28/96V
  160933. A REVIEW. PAQUETTE, L. A. SYNTHETIC ROUTES TO CYCLOPENENOID FUSED UNNATURAL AND NATURAL PRODUCTS. 1984,17, 43. ALDRICHIMICA ACTAa
  160934. GABRIEL WEATHERHEAD
  160935. 9352N
  160936. 2/28/96V
  160937. A REVIEW. WIERSUM, U. E. PREPARATIVE FLASH VACUUM THERMOLYSIS. THE REVIVAL OF PYROLYTIC SYNTHESIS. 1984,17, 31. ALDRICHIMICA ACTAa
  160938. GABRIEL WEATHERHEAD
  160939. 9353N
  160940. 2/28/96V
  160941. A REVIEW. DAVIDSON, R. S.; GOODIN, J. W.; KEMP, G. THE PHOTOCHEMISTRY OF ARYL HALIDES AND RELATED COMPOUNDS. 1984, 20. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  160942. GABRIEL WEATHERHEAD
  160943. 9354N
  160944. 2/28/96V
  160945. A REVIEW.  HAMMERICH, O.; PARKER, V. D. KINETICS AND MECHANISM OF REACTIONS OF ORGANIC CATION RADICALS IN SOLUTION. 1984, 20. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  160946. GABRIEL WEATHERHEAD
  160947. 9355N
  160948. 2/28/96V
  160949. A REVIEW. GOULD, I. R.; TURRO, N. J.; ZIMMI, M. B. MAGNETIC FIELD AND MAGNETIC ISOTOPE EFFECTS ON THE PRODUCTS OF ORGANIC REACTIONS. 1984, 20. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  160950. GABRIEL WEATHERHEAD
  160951. 9356N
  160952. 2/28/96
  160953. A REVIEW. HORWITZ, C. P.; SHRIVER, D. F.  C  AND O BONDED METAL CARBONYL: FORMATION, STRUCTURES, AND REACTIONS. 1984, 23. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160954. GABRIEL WEATHERHEAD
  160955. 9357N
  160956. 2/28/96V
  160957. A REVIEW. BLINKA, T. A.; HELMER, B. J.; WEST, R. POLARIZATION TRANSFER NMR SPECTROSCOPY FOR SILICON 29, THE INEPT AND DEPT TECHNIQUES. 1984, 23. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160958. GABRIEL WEATHERHEAD
  160959. 9358N
  160960. 2/28/96V
  160961. A REVIEW. WIBERG, N. SILYL, GERMYL, AND STANNYL DERIVATIVES OF AZENES NNHN: PART 1: DERIVATIVES OF DIAZENE N2H2. 1984, 23. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160962. GABRIEL WEATHERHEAD
  160963. 9359N
  160964. 2/28/96V
  160965. A REVIEW. GARROU, P. E:. REDISTRIBUTION REACTIORS OF TRANSITION METAL ORGANOMETALLIC COMPLEXES  1984, 23. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160966. GABRIEL WEATHERHEAD
  160967. 9360N
  160968. 2/28/96
  160969. A REVIEW. CONNELLY, N. G.; GEIGER, W. E. THE ELECTRON TRANSFER REACTIONA OF MONONUCLEAR ORGANOTRANSITION METAL COMPLEXES. 1984, 23. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  160970. GABRIEL WEATHERHEAD
  160971. 9361N
  160972. 2/28/96VfA REVIEW. HARDY, C. R. THE CHEMISTRY OF PYRAZOLOPYRIDINES. 1984, 36 ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160973. GABRIEL WEATHERHEAD
  160974. 9362N
  160975. 2/28/96V
  160976. A REVIEW. LUND, H.; TABAKOVIC, I. ELECTROLYSIS OF N HETEROCYCLIC COMPOUNDS (PART II). 1984, 36. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160977. GABRIEL WEATHERHEAD
  160978. 9363N
  160979. 2/28/96V
  160980. A REVIEW.  GALLO, R. J.; MAKOSZA, M.; DOU, H. J. M., HASSANALY, P. APPLICATIONS OF PHASE TRANFER CATALYSIS IN HETEROCYCLIC CHEMISTRY 1984, 36. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160981. GABRIEL WEATHERHEAD
  160982. 9364N
  160983. 2/28/96V
  160984. A REVIEW. CRASS, T. A.; KATRITZKY, A. R. CONFORMATIONAL EQUILIBRIA IN NITROGEN CONTAINING SATURATED SIX MEMBERED RINGS. 1984, 36 ADVANCES IN HETEROCYCLIC CHEMISTRY
  160985. GABRIEL WEATHERHEAD
  160986. 9365N
  160987. 2/28/96VnA REVIEW. SAMMES, M. P.; KATRITZKY, A. R. THE 4H LMIDAZOLES. 1984, 35, 414. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160988. GABRIEL WEATHERHEAD
  160989. 9366N
  160990. 2/28/96VnA REVIEW. SAMMES, M. P.; KATRITZKY, A. R. THE 2H LMIDAZOLES. 1984, 35, 376. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160991. GABRIEL WEATHERHEAD
  160992. 9367N
  160993. 2/28/96V[A REVIEW. SUMMERS, L. A. THE BIPYRIDINES. 1984, 35, 282. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160994. GABRIEL WEATHERHEAD
  160995. 9368N
  160996. 2/28/96V~A REVIEW. RIED, W.; HEINZ B. FOUR MEMBERED RINGS CONTAINING ONE SULFUR ATOM. 1984, 35, 200. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  160997. GABRIEL WEATHERHEAD
  160998. 9369N
  160999. 2/28/96V{A REVIEW. JOULE, J. A. RECENT ADVANCES IN THE CHEMISTRY OF 9H CARBAZOLES. 1984 , 35, 84. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161000. GABRIEL WEATHERHEAD
  161001. 9370N
  161002. 2/28/96
  161003. VgA REVIEW. SARGENT, M. V.; STRANSKY, P. O. DIBENZOFURANS. 1984, 35, 2 ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161004. GABRIEL WEATHERHEAD
  161005. 9371N
  161006. 2/28/96VkA REVIEW. ANTONAKIS, K. KETONUCLEOSIDES. 1984, 42, 227. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  161007. GABRIEL WEATHERHEAD
  161008. 9372N
  161009. 2/28/96V
  161010. A REVIEW. BOCK, K.; PEDERSEN, C.; PEDERSEN, H. CARBON 13 NUCLEAR MAGNETIC RESONANCE DATA FOR OLIGOSACCHARIDES. 1984, 42, 193. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  161011. GABRIEL WEATHERHEAD
  161012. 9373N
  161013. 2/28/96V
  161014. A REVIEW. YAMAMOTO, H.; INOKAWA, S. SUGAR ANALOGS HAVING PHOSPHORUS IN THE HEMIACETAL RING. 1984, 42,136. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  161015. GABRIEL WEATHERHEAD
  161016. 9374N
  161017. 2/28/96V|A REVIEW. YOSHIMURA J. SYNTHESIS OF BRANCHED CHAIN SUGARS. 1984, 42, 69. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  161018. GABRIEL WEATHERHEAD
  161019. 9375N
  161020. 2/28/96
  161021. A REVIEW. ANGYAL, S. J. THE COMPOSITION OF REDUCING SUGARS IN SOLUTION. 1984, 42, 16. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  161022. GABRIEL WEATHERHEAD
  161023. 9376N
  161024. 2/28/96VhA REVIEW. GIESE, B. THE ISOSELECTIVE RELATIONSHIP. 1984,17, 438. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161025. GABRIEL WEATHERHEAD
  161026. 9377N
  161027. 2/28/96V
  161028. A REVIEW.  WILLIAMS, A. EFFECTIVE CHARGE SND LEFFER'S INDEX AS MECHANISTIC TOOLS FOR REACTIONS IN SOLUTION. 1984,17. 425. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161029. GABRIEL WEATHERHEAD
  161030. 9378N
  161031. 2/28/96V
  161032. A REVIEW.  LIGHTNER, D. A.; MCDONAGH, A. F. MOLECULAR MECHANISMS OF PHOTOTHERAPY FOR NEONATAL JAUNDICE. 1984, 17, 417. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161033. GABRIEL WEATHERHEAD
  161034. 9379N
  161035. 2/28/96V
  161036. A REVIEW. KOZIKOWSKI, A. P. THE ISOXAZOLINE ROUTE TO THE MOLECULES OF NATURE. 1984, 17, 410. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161037. GABRIEL WEATHERHEAD
  161038. 2/28/96V
  161039. A REVIEW. HASHIMOTO, Y.; SHUDO, K.; OKAMOTO, T. MUTAGENIC CHEMISTRY OF HETEROAROMATIC AMINES AND MITOMYCIN C. 1984, 17, 403. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161040. GABRIEL WEATHERHEAD
  161041. 9381N
  161042. 2/28/96V
  161043. A REVIEW. HOLLAND, H. L. BIOTRANSFORMATIONS OF D4 3 KETOSTEROIDS BY THE FUNGUS RHIZOPUS ARRHIZUS. 1984,17, 398. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161044. GABRIEL WEATHERHEAD
  161045. 9382N
  161046. 2/28/96VyA REVIEW. WANG, Y. A TOTAL SYNTHESIS OF YEAST ALANINE TRANSFER RNA. 1984,17, 393. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161047. GABRIEL WEATHERHEAD
  161048. 9383N
  161049. 2/28/96VkA REVIEW. WIBERG, K. B. INVERTED GEOMETRIES AT CARBON. 1984,17, 379 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161050. GABRIEL WEATHERHEAD
  161051. 9384N
  161052. 2/28/96V
  161053. A REVIEW. WILLIAMS, D. H. STRUCTURAL STUDIES ON SOME ANTIBIOTICS OF THE VANCOMYCIN GROUP, AND ON THE ANTIBIOTIC RECEPTOR COMPLEXES, BY 1H NMR. 1984,17, 364. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  161054. GABRIEL WEATHERHEAD
  161055. 9385N
  161056. 2/28/96V~A REVIEW. VEDEJS, E. SUFUR MEDIATED RING EXPANSIONS IN TOTAL SYNTHESIS. 1984, 17, 358. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161057. GABRIEL WEATHERHEAD
  161058. 9386N
  161059. 2/28/96VwA REVIEW. STREITWIESER, A., JR. CARBANION ION PAIRS AND TRIPLETS. 1984, 17, 353 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161060. GABRIEL WEATHERHEAD
  161061. 9387N
  161062. 2/28/96VyA REVIEW. CHILDS, R. F. THE HOMOTROPYLIUM ION AND HOMOAROMATICITY. 1984, 17, 347. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161063. GABRIEL WEATHERHEAD
  161064. 9388N
  161065. 2/28/96V
  161066. A REVIEW. OISHI, T.; NAKATA, T. AN INTRODUCTION OF CHIRAL CENTERS INTO ACYCLIC SYSTEMS BASED ON STEREOSELECTIVE KETONE REDUCTION. 1984, 17, 338. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161067. GABRIEL WEATHERHEAD
  161068. 9389N
  161069. 2/28/96
  161070. A REVIEW.  GLADYSZ, J. A. NEW SYNTHETIC CHEMISTRY OF TRANSITION METAL TRIALKYLSILANE COMPLEXES. 1984, 17, 326 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161071. GABRIEL WEATHERHEAD
  161072. 9390N
  161073. 2/28/96V
  161074. A REVIEW. TAYLOR, R.; KENNARD, O. HYDROGEN BOND GEOMETRY IN ORGANIC CRYSTALS. 1984 17, 320. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161075. GABRIEL WEATHERHEAD
  161076. 9391N
  161077. 2/28/96V|A REVIEW. KIRBY, A. J. STEREOELECTRONIC EFFECTS ON ACETAL HYDROLYSIS. 1984, 17, 305. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161078. GABRIEL WEATHERHEAD
  161079. 9392N
  161080. 2/28/96V
  161081. A REVIEW. STEVENS, R. V. NUCLEOPHILIC ADDITIONS TO TETRAHYDROPYRIDINIUM SALTS. APPLICATIONS TO ALKALOID SYNTHESES. 1984, 17, 289 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161082. GABRIEL WEATHERHEAD
  161083. 9393N
  161084. 2/28/96V
  161085. A REVIEW. CRILLER, D.; NAZRAN, A. S.; SCAIANO, J. C. FLASH PHOTOLYSIS STUDIES OF CARBENES AND THEIR REACTION KINETICS. 1984, 17, 283. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  161086. GABRIEL WEATHERHEAD
  161087. 9394N
  161088. 2/28/96V
  161089. A REVIEW. SIMON, J. D.; PETERS, K. S. PICOSECOND STUDIES OF ORGANIC PHOTOREACTIONS. 1984, 17, 277 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161090. GABRIEL WEATHERHEAD
  161091. 9395N
  161092. 2/28/96V
  161093. A REVIEW. REBEK, J., JR. BINDING FORCES, EQUILIBRIA, AND RATES: NEW MODES FOR ENZYMIC CATALYSIS. 1984, 17, 258. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161094. GABRIEL WEATHERHEAD
  161095. 9396N
  161096. 2/28/96V
  161097. A REVIEW.  PARKER V. D. REACTION PATHWAYS OF THE CATION RADICALS OF AROMATIC COMPOUNDS RELATED TO THE ANTHRACENES. 1984, 17, 243. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161098. GABRIEL WEATHERHEAD
  161099. 9397N
  161100. 2/28/96VQA REVIEW. WAKEFIELD, B. J. ORGANOLITHIUM METHODS. ACADEMIC PRESS: NEW YORK, 1988.a
  161101. GABRIEL WEATHERHEAD
  161102. 9398N
  161103. 2/28/96VsA REVIEW. TOWNSEND, LEROY B., ED. CHEMISTRY OF NUCLEOSIDES AND NUCLEOTIDES, VOLUME 1. PLENUM PRESS: NEW YORK, 1988.a
  161104. GABRIEL WEATHERHEAD
  161105. 9399N
  161106. 2/28/96V
  161107. A REVIEW. TORSELL, K. B. G. NITRILE OXIDES, NITRONES AND NITRONATES IN ORGANIC SYNTHESIS. NOVEL STRATEGIES IN SYNTHESIS. VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG, 1988.a
  161108. GABRIEL WEATHERHEAD
  161109. 9400N
  161110. 2/28/96V{A REVIEW. SHERRINGTON, D. C.; HODGE, P. SYNTHESES AND SEPARATIONS USING FUNCTIONAL POLYMERS. WILEY: CHICHESTER, U.K., 1988.a
  161111. GABRIEL WEATHERHEAD
  161112. 9401N
  161113. 2/28/96VeA REVIEW. REMERS, WILLIAM A. THE CHEMISTRY OF ANTITUMOR ANTIBIOTICS, VOLUME 2. WILEY: NEW YORK, 1988.a
  161114. GABRIEL WEATHERHEAD
  161115. 9402N
  161116. 2/28/96V
  161117. A REVIEW. REICHARDT, CHRISTIAN. SOLVENTS AND SOLVENT EFFECTS IN ORGANIC CHEMISTRY, 2ND ED. VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG, 1988.a
  161118. GABRIEL WEATHERHEAD
  161119. 9403N
  161120. 2/28/96VwA REVIEW.  RAHMAN, ATTA UR; LEQUESNE, PHILIP WILLIAM, EDS. NATURAL PRODUCTS CHEMISTRY III. SPRINGER: BERLIN, FRG, 1988.a
  161121. GABRIEL WEATHERHEAD
  161122. 9404N
  161123. 2/28/96
  161124. @VoA REVIEW.  PELTER, ANDREW, SMITH, KEITH, BROWN, HERBERT C. BORANE REAGENTS. ACADEMIC PRESS: LONDON, U.K., 1988.a
  161125. GABRIEL WEATHERHEAD
  161126. 9405N
  161127. 2/28/96V
  161128. A REVIEW. PATAI, SAUL; RAPPOPORT, ZVI; EDS. THE CHEMISTRY OF THE QUINONOID COMPOUNDS, VOLUME 2, PTS. 1 AND 2. WILEY: CHICHESTER, U.K., 1988.a
  161129. GABRIEL WEATHERHEAD
  161130. 9406N
  161131. 2/28/96VpA REVIEW. MUNDY, B. P.; ELLERD, M. G. NAME REACTIONS AND REAGENTS IN ORGANIC SYNTHESIS. WILEY: CHICHESTER, U.K.,a
  161132. GABRIEL WEATHERHEAD
  161133. 9407N
  161134. 2/28/96V
  161135. A REVIEW. LIPCZYNSKA KOCHANY, EWA. SOME NEW ASPECTS OF HYDROXAMIC ACIDS CHEMISTRY. WYDAWN. POLITECH. WARSZ.: WARSAW, POLAND, 1988.a
  161136. GABRIEL WEATHERHEAD
  161137. 9408N
  161138. 2/28/96VwA REVIEW. LINDBERG, THOMAS, ED. STRATEGIES AND TACTICS IN ORGANIC SYNTHESIS, VOLUME 2. ACADEMIC PRESS: SAN DIEGO, 1988.a
  161139. GABRIEL WEATHERHEAD
  161140. 9409N
  161141. 2/28/96
  161142. A REVIEW. LE NOBLE, W. J., ED. ORGANIC HIGH PRESSURE CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY, VOL. 37). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1988.a
  161143. GABRIEL WEATHERHEAD
  161144. 9410N
  161145. 2/28/96VzA REVIEW. KRIEF, A.; HEVESI, L. ORGANOSELENIUM CHEMISTRY I. FUNCTIONAL GROUP TRANSFORMATIONS. SPRINGER: BERLIN, FRG, 1988.a
  161146. GABRIEL WEATHERHEAD
  161147. 9411N
  161148. 2/28/96V
  161149. A REVIEW.  KRASOVITSKII, B. M.; BOLOTIN, B. M. ORGANIC LUMINESCENT MATERIALS. VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG (TRANSLATED FROM THE RUSSIAN), 1988.a
  161150. GABRIEL WEATHERHEAD
  161151. 9412N
  161152. 2/28/96V
  161153. A REVIEW. HORTON, DEREK, HAWKINS, LYNN D., MCGARVEY, GLENN J. EDS. TRENDS IN SYNTHETIC CARBOHYDRATE CHEMISTRY (ACS SYMPOSIUM SERIES, NO. 386). AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC, 1989.a
  161154. GABRIEL WEATHERHEAD
  161155. 9413N
  161156. 2/28/96VlA REVIEW. HO, TSE LOK. CARBOCYCLE CONSTRUCTION IN TERPENE SYNTHESIS. VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG,a
  161157. GABRIEL WEATHERHEAD
  161158. 9414N
  161159. 2/28/96
  161160. A REVIEW. HARGITTAI, ISTVAN; HARGITTAI, MAGDOLNA, EDS. STEREOCHEMICAL APPLICATIONS OF GAS PHASE ELECTRON DIFFRACTION PART B: STRUCTURAL INFORMATION FOR SELECTED CLASSES OF COMPOUNDS. [IN: METHODS STEREOCHEM. ANAL., 1988, 10] VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG, 1988.
  161161. GABRIEL WEATHERHEAD
  161162. 9415N
  161163. 2/28/96VqA REVIEW. HARBORNE, J. B., ED. THE FLAVONOIDS. ADVANCES IN RESEARCH SINCE 1980. CHAPMAN AND HALL: NEW YORK, 1988.a
  161164. GABRIEL WEATHERHEAD
  161165. 9416N
  161166. 2/28/96V
  161167. A REVIEW. GUPTA, R. R., ED. BIOACTIVE MOLECULES, VOL. 4: PHENOTHIAZINES AND 1,4 BENZOTHIAZINES: CHEMICAL AND BIOMEDICAL ASPECTS. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1988.a
  161168. GABRIEL WEATHERHEAD
  161169. 9417N
  161170. 2/28/96V
  161171. A REVIEW. FISCHER, H.; HOFMANN, P.; KREISSL, F. R.; SCHROCK, R. R.; SCHUBERT, U., WEISS, K. CARBYNE COMPLEXES. VCH VERLAGSGESELLSCHAFT: WEINHEIM, FRG, 1988.a
  161172. GABRIEL WEATHERHEAD
  161173. 2/28/96V
  161174. A REVIEW.  DE KIMPE, ROBERT; VERHE, ROLAND. THE CHEMISTRY OF A HALO KETONES, A HALO ALDEHYDES, AND A HALO IMINES. WILEY: CHICHESTER, U.K., 1988.a
  161175. GABRIEL WEATHERHEAD
  161176. 9419N
  161177. 2/28/96V
  161178. A REVIEW. BRANDSMA, L., ED. PREPARATIVE ACETYLENIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY, VOL. 34), 2ND ED. ELSEVIER, AMSTERDAM, THE NETHERLANDS, 1988.a
  161179. GABRIEL WEATHERHEAD
  161180. 9420N
  161181. 2/28/96VfA REVIEW. APSIMON, JOHN, ED. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOLUME 7. WILEY: NEW YORK, 1988.a
  161182. GABRIEL WEATHERHEAD
  161183. 9421N
  161184. 2/28/96V
  161185. A REVIEW. ALLENMARK, STIG G. CHROMATOGRAPHIC ENANTIOSEPARATION: METHODS AND APPLICATIONS. ELLIS HORWOOD LTD./WILEY: CHICHESTER, U.K., 1988.a
  161186. GABRIEL WEATHERHEAD
  161187. 9422N
  161188. 2/28/96
  161189. ?A REVIEW.  LIEBMAN, J. F. FLUORINE CHEMISTRY WITHOUT FLUORINE: SUBSTITUENT EFFECTS AND EMPIRICAL MIMICRY. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161190. GABRIEL WEATHERHEAD
  161191. 9423N
  161192. 2/28/96
  161193. ;A REVIEW. BERGSTROM, D. E., SWARTLING, D. J. FLUORINE SUBSTITUTED ANALOGS OF NUCLEIC ACID COMPONENTS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161194. GABRIEL WEATHERHEAD
  161195. 9424N
  161196. 2/28/96
  161197. *A REVIEW. PETERS, N. J. S., ALLEN, L. C. STRUCTURE AND BONDING IN N, O, F COMPOUNDS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161198. GABRIEL WEATHERHEAD
  161199. 9425N
  161200. 2/28/96
  161201. A REVIEW. JACHE, A. W. THE INORGANIC CHEMISTRY OF HYDROGEN FLUORIDE. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161202. GABRIEL WEATHERHEAD
  161203. 9426N
  161204. 2/28/96
  161205. NA REVIEW.  BURTON, D. J. STEREOSPECIFIC PREPARATION, REACTIVITY, AND UTILITY OF POLYFLUORINATED ALKENYL ORGANOMETALLICS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161206. GABRIEL WEATHERHEAD
  161207. 9427N
  161208. 2/28/96
  161209. ?A REVIEW. WELCH, J. T. ESWARAKRISHNAN, S. THE EFFECT OF FLUORINATION OF ENOLATES AND ENOLATE EQUIVALENTS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161210. GABRIEL WEATHERHEAD
  161211. 9428N
  161212. 2/28/96
  161213. ?A REVIEW.  KOCH, H. F.; KOCH, J. G. PARTITIONING OF CARBANION INTERMEDIATES GENERATED IN ALCOHOLIC MEDIA. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161214. GABRIEL WEATHERHEAD
  161215. 9429N
  161216. 2/28/96
  161217. 2A REVIEW. BUMGARDNER, C. L.; WHANGBO, M. H. SECONDARY ORBITAL EFFECTS IN FLUORINE COMPOUNDS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161218. GABRIEL WEATHERHEAD
  161219. 9430N
  161220. 2/28/96
  161221. LA REVIEW.  DOLBIER, W. R., JR.; KORONIAK, H. K. THE ELECTROCYCLIC RING OPENING OF FLUORINATED CYCLOBUTENE DERIVATIVES. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161222. GABRIEL WEATHERHEAD
  161223. 9431N
  161224. 2/28/96
  161225. SA REVIEW. SKANCKE, A. THE EFFECT OF FLUORINE AS A SUBSTITUENT ON SELECTED PROPERTIES OF NEUTRAL AND CHARGED AROMATIC SYSTEMS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161226. GABRIEL WEATHERHEAD
  161227. 9432N
  161228. 2/28/96
  161229. >A REVIEW. FILLER, R. NONBONDED INTERACTIONS BETWEEN ARENES AND POLYFLUOROARENES: STRUCTURE AND DYNAMICS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161230. GABRIEL WEATHERHEAD
  161231. 9433N
  161232. 2/28/96
  161233. ;A REVIEW. RAHMAN, M.; MCKEE, M. L.; SHEVLIN, P. B. THE REACTIONS OF ATOMIC CARBON WITH FLUOROCARBONS. FLUORINE CONTAINING MOLECULES. STRUCTURE, REACTIVITY, SYNTHESIS AND APPLICATIONS (MOLECULAR STRUCTURE AND ENERGETICS, VOL. 8), J. F. LIEBMAN, A. GREENBERG, W. R. DOLBIER, JR., EDS., VCH PUBLISHERS: NEW YORK, 1988.
  161234. GABRIEL WEATHERHEAD
  161235. 9434N
  161236. 2/28/96V
  161237. A REVIEW.  HIEMSTRA, H., SPECKAMP, W. N. N ACYLIMINIUM IONS AS INTERMEDIATES IN ALKALOID SYNTHESIS. THE ALKALOIDS, VOLUME 32. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.
  161238. GABRIEL WEATHERHEAD
  161239. 9435N
  161240. 2/28/96V
  161241. A REVIEW. GRUNDON, M. F. QUINOLINE ALKALOIDS RELATED TO ANTHRANILIC ACID. THE ALKALOIDS, VOLUME 32. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  161242. GABRIEL WEATHERHEAD
  161243. 9436N
  161244. 2/28/96V
  161245. A REVIEW. RAHMAN, ATTA UR; MUZAFFAR, A. STEROIDAL ALKALOIDS OF APOCYNACEAE AND BUXACEAE. THE ALKALOIDS, VOLUME 32. CHEMISTRY AND PHARMACOLOGY, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  161246. GABRIEL WEATHERHEAD
  161247. 9437N
  161248. 2/28/96V
  161249. A REVIEW. CURRAN, D. P. THE CYCLOADDITION APPROACH TO ALPHA HYDROXY CARBONYLS: AN EMERGING ALTERNATIVE TO THE ALDOL STRATEGY. ADVANCES IN CYCLOADDITION. VOLUME 1, D. P. CURRAN, ED., JAI PRESS, INC.: GREENWICH, CT, 1988.a
  161250. GABRIEL WEATHERHEAD
  161251. 9438N
  161252. 2/28/96
  161253. A REVIEW. DESHONG, P.; LANDER, S. W., JR.; LEGINUS, J. M.; DIEKSON, C. M. DIPOLAR CYCLOADDITIONS OF NITRONES WITH VINYL ETHERS AND SILANE DERIVATIVES. ADVANCES IN CYCLOADDITION. VOLUME 1, D. P. CURRAN, ED., JAI PRESS, INC.: GREENWICH, CT, 1988.a
  161254. GABRIEL WEATHERHEAD
  161255. 9439N
  161256. 2/28/96V
  161257. A REVIEW. SCHULTZ, A. G. MOLECULAR REARRANGEMENTS OCCURRING FROM PRODUCTS OF INTRAMOLECULAR 1,3 DIPOLAR CYCLOADDITIONS: SYNTHETIC AND MECHANISTIC ASPECTS. ADVANCES IN CYCLOADDITION. VOLUME 1, D. P. CURRAN, ED., JAI PRESS, INC.: GREENWICH, CT, 1988.a
  161258. GABRIEL WEATHERHEAD
  161259. 9440N
  161260. 2/28/96V
  161261. A REVIEW. VEDEJS, E. NONSTABILIZED AZOMETHINE YLIDES. ADVANCES IN CYCLOADDITION. VOLUME 1, D. P. CURRAN, ED., JAI PRESS, INC.: GREENWICH, CT, 1988.a
  161262. GABRIEL WEATHERHEAD
  161263. 9441N
  161264. 2/28/96
  161265. A REVIEW.  HUISGEN, R. STERIC COURSE AND MECHANISM OF 1,3 DIPOLAR CYCLOADDITIONS. ADVANCES IN CYCLOADDITION. VOLUME 1, D. P. CURRAN, ED., JAI PRESS, INC.: GREENWICH, CT, 1988.a
  161266. GABRIEL WEATHERHEAD
  161267. 9442N
  161268. 2/28/96VdA REVIEW. KAGAN, H. B.; FIAUD, J. C. KINETIC RESOLUTION. 1988,18, 249 330. TOPICS IN STEREOCHEMISTRYa
  161269. GABRIEL WEATHERHEAD
  161270. 9443N
  161271. 2/28/96V
  161272. A REVIEW. BRUNNER, HENRI. ENANTIOSELECTIVE SYNTHESIS OF ORGANIC COMPOUNDS WITH OPTICALLY ACTIVE TRANSITION METAL CATALYSTS IN SUBSTOICHIOMETRIC QUANTITIES. 1988,18,129 247. TOPICS IN STEREOCHEMISTRYa
  161273. GABRIEL WEATHERHEAD
  161274. 9444N
  161275. 2/28/96V
  161276. A REVIEW. PORTER, N. A.; KREBS, P. J. STEREOCHEMICAL ASPECTS OF RADICAL PAIR REACTIONS. 1988,18, 97 127. TOPICS IN STEREOCHEMISTRYa
  161277. GABRIEL WEATHERHEAD
  161278. 9445N
  161279. 2/28/96VnA REVIEW. BONNER, WILLIAM A. ORIGINS OF CHIRAL HOMOGENEITY IN NATURE. 1988,18, 1 96. TOPICS IN STEREOCHEMISTRYa
  161280. GABRIEL WEATHERHEAD
  161281. 9446N
  161282. 2/28/96V
  161283. A REVIEW. TODA, F. REACTION CONTROL OF GUEST COMPOUNDS IN HOST GUEST INCLUSION COMPLEXES. 1988,149(MOLECULAR INCLUSION & MOLEC. RECOGNITION CLATHRATES 2), 211 238. TOPICS IN CURRENT CHEMISTRYa
  161284. GABRIEL WEATHERHEAD
  161285. 9447N
  161286. 2/28/96V
  161287. A REVIEW.  REBEK, J., JR. RECENT PROGRESS IN MOLECULAR RECOGNITION. 1988, 149(MOLECULAR INCLUSION & MOLEC. RECOGNITION CLATHRATES 2), 189 210. TOPICS IN CURRENT CHEMISTRYa
  161288. GABRIEL WEATHERHEAD
  161289. 9448N
  161290. 2/28/96V
  161291. A REVIEW. BISHOP, R.; DANCE, I. G. NEW TYPES OF HELICAL CANAL INCLUSION NETWORKS. 1988,149(MOLECULAR INCLUSION & MOLEC. RECOGNITION CLATHRATES 2), 137 188. TOPICS IN CURRENT CHEMISTRYa
  161292. GABRIEL WEATHERHEAD
  161293. 9449N
  161294. 2/28/96V
  161295. A REVIEW. WEBER, E.; CZUGLER, M. FUNCTIONAL GROUP ASSISTED CLATHRATE FORMATION
  161296. SCISSOR LIKE AND ROOF SHAPED HOST MOLECULES. 1988,149(MOLECULAR INCLUSION & MOLEC. RECOGNITION CLATHRATES 2), 45 135. TOPICS IN CURRENT CHEMISTRY
  161297. GABRIEL WEATHERHEAD
  161298. 9450N
  161299. 2/28/96V
  161300. A REVIEW.  GOLDBERG, I. THE SIGNIFICANCE OF MOLECULAR TYPE, SHAPE AND COMPLEMENTARITY IN CLATHRATE INCLUSION. 1988, 149 (MOLECULAR INCLUSION & MOLEC. RECOGNITION CLATHRATES 2), 1 44. TOPICS IN CURRENT CHEMISTRYa
  161301. GABRIEL WEATHERHEAD
  161302. 9451N
  161303. 2/28/96V
  161304. A REVIEW. RABINOVITZ,MORDECAI. POLYCYCLIC ANIONS: FROM DOUBLY TO HIGHLY CHARGED P CONJUGATED SYSTEMS. 1988,146(PHYS. ORG. CHEM.), 99 169. TOPICS IN CURRENT CHEMISTRYa
  161305. GABRIEL WEATHERHEAD
  161306. 9452N
  161307. 2/28/96V
  161308. A REVIEW. KAUPP, GERD. COMPLEX ELIMINATIONS; ELIMINATIONS WITH REARRANGEMENTS. 1988,146(PHYS. ORG. CHEM.), 57 98. TOPICS IN CURRENT CHEMISTRYa
  161309. GABRIEL WEATHERHEAD
  161310. 9453N
  161311. 2/28/96VuA REVIEW. BOCHE, GERNOT. REARRANGEMENTS OF CARBANIONS. 1988, 146(PHYS. ORG. CHEM.), 1 56. TOPICS IN CURRENT CHEMISTRYa
  161312. GABRIEL WEATHERHEAD
  161313. 9454N
  161314. 2/28/96
  161315. A REVIEW. BAIRD, MARK S. FUNCTIONALIZED CYCLOPROPENES AS SYNTHETIC INTERMEDIATES. 1988,144(SMALL RING COMPD. ORG. SYNTH. 3), 137 209. TOPICS IN CURRENT CHEMISTRYa
  161316. GABRIEL WEATHERHEAD
  161317. 9455N
  161318. 2/28/96V
  161319. A REVIEW. REISSIG, HANS ULRICH. DONOR ACCEPTOR SUBSTITUTED CYCLOPROPANES: VERSATILE BUILDING BLOCKS IN ORGANIC SYNTHESIS. 1988,144(SMALL RING COMPD. ORG. SYNTH. 3), 73 135. TOPICS IN CURRENT CHEMISTRYa
  161320. GABRIEL WEATHERHEAD
  161321. 9456N
  161322. 2/28/96V
  161323. A REVIEW. SALAUN, JACQUES R. Y. SYNTHESIS AND SYNTHETIC APPLICATIONS OF L DONOR SUBSTITUTED CYCLOPROPANES WITH ETHYNYL, VINYL, AND CARBONYL GROUPS. 1988,144(SMALL RING COMPD. ORG. SYNTH. 3),1 71. TOPICS IN CURRENT CHEMISTRYa
  161324. GABRIEL WEATHERHEAD
  161325. 9457N
  161326. 2/28/96V
  161327. A REVIEW. OBERHAUSER, T.; FABER, K.; GRIENGL, H. A SUBSTRATE MODEL FOR THE ENZYMIC RESOLUTION OF ESTERS OF BICYCLIC ALCOHOLS BY CANDIDA CYLINDRACEA LIPASE. 1989, 45(6),1679 82. TETRAHEDRONa
  161328. GABRIEL WEATHERHEAD
  161329. 9458N
  161330. 2/28/96VlA REVIEW.  SORRELL, THOMAS N. SYNTHETIC MODELS FOR BINUCLEAR COPPER PROTEINS. 1989, 45(1), 3 68. TETRAHEDRONa
  161331. GABRIEL WEATHERHEAD
  161332. 9459N
  161333. 2/28/96V\A REVIEW. CREMER, DIETER. PROS AND CONS OF S AROMATICITY. 1988, 44(24), 7427 54. TETRAHEDRONa
  161334. GABRIEL WEATHERHEAD
  161335. 9460N
  161336. 2/28/96VuA REVIEW.  THIEL, WALTER. SEMIEMPIRICAL METHODS: CURRENT STATUS AND PERSPECTIVES. 1988, 44(24), 7393 408. TETRAHEDRONa
  161337. GABRIEL WEATHERHEAD
  161338. 9461N
  161339. 2/28/96V
  161340. A REVIEW. DE LUCCHI, OTTORINO; PASQUATO, LUCIA. THE ROLE OF SULFUR FUNCTIONALITIES IN ACTIVATING AND DIRECTING OLEFINS IN CYCLOADDITION REACTIONS. 1988, 44(22), 6755 94. TETRAHEDRONa
  161341. GABRIEL WEATHERHEAD
  161342. 9462N
  161343. 2/28/96VhA REVIEW. MADESELAIRE, MICHEL. REDUCTION OF SULFOXIDES TO THIOETHERS. 1988, 44(21), 6537 80. TETRAHEDRONa
  161344. GABRIEL WEATHERHEAD
  161345. 9463N
  161346. 2/28/96
  161347. A REVIEW. GUZIEC, FRANK S., JR.; SANFILIPPO, LYNN JAMES. SYNTHETICALLY USEFUL EXTRUSION REACTIONS OF ORGANIC SULFUR, SELENIUM AND TELLURIUM COMPOUNDS. 1988, 44(20), 6241 85. TETRAHEDRONa
  161348. GABRIEL WEATHERHEAD
  161349. 9464N
  161350. 2/28/96V
  161351. A REVIEW. BRESLOW, RONALD; CHMIELEWSKI, DEAN; FOLEY, DIANE; JOHNSON, BRUCE, KUMABE, NAOFUMI, VARNEY, MICHAEL; MEHRA, RAJ. OPTICALLY ACTIVE AMINO ACID SYNTHESIS BY ARTIFICIAL TRANSAMINASE ENZYMES. 1988, 44(17), 5515 24. TETRAHEDRONa
  161352. GABRIEL WEATHERHEAD
  161353. 9465N
  161354. 2/28/96V
  161355. A REVIEW.  DREWES, SIEGFRIED E.; ROOS, GREGORY H. P. SYNTHETIC POTENTIAL OF THE TERTIARY AMINE CATALYZED REACTION OF ACTIVATED VINYL CARBANIONS WITH ALDEHYDES. 1988, 44(15), 4653 70. TETRAHEDRONa
  161356. GABRIEL WEATHERHEAD
  161357. 9466N
  161358. 2/28/96V
  161359. A REVIEW. WEISS, RIEHARD G. THERMOTROPIC LIQUID CRYSTALS AS REACTION MEDIA FOR MECHANISTIC INVESTIGATIONS. 1988, 44(12), 3413 75. TETRAHEDRONa
  161360. GABRIEL WEATHERHEAD
  161361. 9467N
  161362. 2/28/96
  161363. A REVIEW. RODRIGO, RUSSELL. PROGRESS IN THE CHEMISTRY OF ISOBENZOFURANS, APPLICATIONS TO THE SYNTHESIS OF NATURAL PRODUCTS AND POLYAROMATIC HYDROCARBONS. 1988, 44(8), 2093 135. TETRAHEDRONa
  161364. GABRIEL WEATHERHEAD
  161365. 9468N
  161366. 2/28/96VoA REVIEW. BILLUPS, W. E., RODIN, WAYNE A., HALEY, MICHAEL M. CYCLOPROPARENES. 1988, 44(5), 1305 38. TETRAHEDRONa
  161367. GABRIEL WEATHERHEAD
  161368. 9469N
  161369. 2/28/96V
  161370. A REVIEW. CHUPAKHIN, O. N.; CHARUSHIN, V. N.; VAN DER PLAS, HENK C. NUCLEOPHILIC SUBSTITUTION OF HYDROGEN IN AZINES. 1988 44(1), 1 34. TETRAHEDRONa
  161371. GABRIEL WEATHERHEAD
  161372. 9470N
  161373. 2/28/96VAA REVIEW.  GANTE, J. AZAPEPTIDES. 1989, NO. 6, 405 413. SYNTHESISa
  161374. GABRIEL WEATHERHEAD
  161375. 9471N
  161376. 2/28/96VuA REVIEW. GREE, R. ACYCLIC BUTADIENE IRON TRICARBONYL COMPLEXES IN ORGANIC SYNTHESIS. 1989, NO. 5, 341 355. SYNTHESISa
  161377. GABRIEL WEATHERHEAD
  161378. 9472N
  161379. 2/28/96
  161380. ViA REVIEW. MATTAY, J. PHOTOINDUCED ELECTRON TRANSFER IN ORGANIC SYNTHESIS. 1989, NO. 4, 233 252. SYNTHESISa
  161381. GABRIEL WEATHERHEAD
  161382. 9473N
  161383. 2/28/96VzA REVIEW. DEMUTH, M.; MIKHAIL, G. NEW DEVELOPMENTS IN THE FIELD OF PHOTOCHEMICAL SYNTHESIS. 1989, NO. 3,145 162. SYNTHESISa
  161384. GABRIEL WEATHERHEAD
  161385. 9474N
  161386. 2/28/96VgA REVIEW. BLECHERT, S. THE HETERO COPE REARRANGEMENT IN ORGANIC SYNTHESIS. 1989, NO. 2,71 82. SYNTHESISa
  161387. GABRIEL WEATHERHEAD
  161388. 9475N
  161389. 2/28/96VjA REVIEW.  COOLEY, J. H. ELVAIN, E. J. AMINE DEALKYLATIONS WITH ACYL CHLORIDES. 1989, NO. 1,1 7. SYNTHESISa
  161390. GABRIEL WEATHERHEAD
  161391. 9476N
  161392. 2/28/96
  161393. A REVIEW. KAISER, EMIL THOMAS; MIHARA, HISAKAZU; LAFORET, GENEVIEVE A., KELLEY, JEFFERY W., WALTERS, LEE; FINDEIS MARK A.; SASAKI, TOMIKAZU. PEPTIDE AND PROTEIN SYNTHESIS BY SEGMENT SYNTHESIS CONDENSATION. 1989, 243(4888), 187 92. SCIENCE (WASHINGTON, DC 1883 )
  161394. GABRIEL WEATHERHEAD
  161395. 9477N
  161396. 2/28/96VoA REVIEW.  KROTO, HAROLD. SPACE, STARS, C60, AND SOOT. 1988, 242(4882), 1139 45. SCIENCE (WASHINGTON, DC 1883 )a
  161397. GABRIEL WEATHERHEAD
  161398. 9478N
  161399. 2/28/96V
  161400. A REVIEW. ARSHINOVA, R. P. CONTEMPORARY IDEAS ABOUT THE CONFORMATIONS OF EIGHT MEMBERED CYCLIC SYSTEMS WITH PLANAR FRAGMENTS. 1988, 57(12), 1142 1161. RUSSIAN CHEMICAL REVIEWSa
  161401. GABRIEL WEATHERHEAD
  161402. 9479N
  161403. 2/28/96V
  161404. A REVIEW. KAZANSKII, V. B. MODERN IDEAS ABOUT THE MECHANISM OF HOMOGENEOUS AND HETEROGENEOUS ACID CATALYSIS: SIMILARITIES AND DIFFERENCES. 1988, 57(12),1109 1123. RUSSIAN CHEMICAL REVIEWSa
  161405. GABRIEL WEATHERHEAD
  161406. 9480N
  161407. 2/28/96V
  161408. A REVIEW.  USYATINSKII, A. YA.; BREGADZE, V. 1. ARYL DERIVATIVES OF THALLIUM(ILI): PREPARATION AND USE IN ORGANIC SYNTHESIS. 1988, 57(11) 1054 1068. RUSSIAN CHEMICAL REVIEWSa
  161409. GABRIEL WEATHERHEAD
  161410. 9481N
  161411. 2/28/96
  161412. A REVIEW. ZEFIROV, N. S., ZHDANKIN, V. V., KOZ'MIN, A. S. THE SYNTHESIS AND PROPERTIES OF COVALENT ORGANIC PERCHLORATES. 1988, 57(11), 1041 1053. RUSSIAN CHEMICAL REVIEWSa
  161413. GABRIEL WEATHERHEAD
  161414. 9482N
  161415. 2/28/96VeA REVIEW. FEDOROV, L. A. NMR SPECTROSCOPY OF AZO DYES. 1988 57(10), 941 955. RUSSIAN CHEMICAL REVIEWSa
  161416. GABRIEL WEATHERHEAD
  161417. 9483N
  161418. 2/28/96V|A REVIEW.  KARPYSHEV, N. N. PHOSPHITE SYNTHESIS OF OLIGODEOXYRIBONUCLEOTIDES. 1988, 57(9), 886 896. RUSSIAN CHEMICAL REVIEWSa
  161419. GABRIEL WEATHERHEAD
  161420. 9484N
  161421. 2/28/96VqA REVIEW. KADRYOV, A. A.; ROKHLIN, E. M. FLUORALKENYLPHOSPHONATES. 1988, 57(9), 852 863. RUSSIAN CHEMICAL REVIEWSa
  161422. GABRIEL WEATHERHEAD
  161423. 9485N
  161424. 2/28/96V
  161425. A REVIEW. BAKHMUTOV, V. I.; GALAKHOV, M. V. NMR SPECTROSCOPY OF POLYFLUORINATED ALLYL CATIONS. 1988, 57(9), 839 851. RUSSIAN CHEMICAL REVIEWSa
  161426. GABRIEL WEATHERHEAD
  161427. 9486N
  161428. 2/28/96
  161429. A REVIEW. KHRAMTSOV, V. V.; VAINER, L. M. PHOTON TRANSFER REACTIONS IN FREE RADICALS. SPIN PH PROBES. 1988, 57(9) 824 838. RUSSIAN CHEMICAL REVIEWSa
  161430. GABRIEL WEATHERHEAD
  161431. 9487N
  161432. 2/28/96V
  161433. A REVIEW. HO, T. L. CONTRAPOLARIZATION, A NEW CONCEPT IN ORGANIC REACTIVITY. 1989, 11(2), 157 224. RESEARCH ON CHEMICAL INTERMEDIATESa
  161434. GABRIEL WEATHERHEAD
  161435. 9488N
  161436. 2/28/96V{A REVIEW.  ANKLAM, E., MARGARETHA, P. ORGANIC SULFURANYL RADICALS. 1989, 11(2), 127 155. RESEARCH ON CHEMICAL INTERMEDIATESa
  161437. GABRIEL WEATHERHEAD
  161438. 9489N
  161439. 2/28/96V
  161440. A REVIEW. OLOFSON, ROY A. NEW, USEFUL REACTIONS OF NOVEL HALOFORMATES AND RELATED REAGENTS. 1988, 60(11),1715 24. PURE AND APPLIED CHEMISTRYa
  161441. GABRIEL WEATHERHEAD
  161442. 9490N
  161443. 2/28/96
  161444. A REVIEW. GUINDON, YVAN; ANDERSON, PAUL C.; YOAKIM, CHRISTIANE; GIRARD, YVES, BERTHIAUME, SYLVIE, MORTON, HOWARD E. NEW SYNTHETIC APPLICATIONS OF DIALKYLBORON HALIDE REAGENTS. 1988, 60(11), 1705 14. PURE AND APPLIED CHEMISTRYa
  161445. GABRIEL WEATHERHEAD
  161446. 9491N
  161447. 2/28/96V
  161448. A REVIEW.  SOLLADIE, GUY. RECENT RESULTS IN THE FIELD OF ASYMMETRIC SYNTHESIS USING CHIRAL SULFOXIDES. 1988, 60(11),1699 704. PURE AND APPLIED CHEMISTRYa
  161449. GABRIEL WEATHERHEAD
  161450. 9492N
  161451. 2/28/96V
  161452. A REVIEW. GUETTE, JEAN PAUL; CREENE, NOEL, BULLIOT, HENRI, DESMURS JEAN ROGER; IGERSHEIM, FRANCOISE. AUTOMATION IN THE ORGANIC CHEMISTRY LABORATORY: WHY? HOW? 1988, 60(11),1669 78 PURE AND APPLIED CHEMISTRYa
  161453. GABRIEL WEATHERHEAD
  161454. 9493N
  161455. 2/28/96V
  161456. A REVIEW. SURZUR, JEAN MARIE; BERTRAND, MICHELE PAULA. LACTONE SYNTHESIS BY ELECTRON TRANSFER AND RADICAL CHEMISTRY. 1988, 60(11), 1659 68. PURE AND APPLIED CHEMISTRYa
  161457. GABRIEL WEATHERHEAD
  161458. 9494N
  161459. 2/28/96
  161460. V}A REVIEW. GIESE, BERND. STEREOSELECTIVE SYNTHESES WITH CARBOHYDRATE RADICALS. 1988, 60(11),1655 8. PURE AND APPLIED CHEMISTRYa
  161461. GABRIEL WEATHERHEAD
  161462. 9495N
  161463. 2/28/96VqA REVIEW. SCHLOSSER, MANFRED. SUPERBASES FOR ORGANIC SYNTHESIS. 1988, 60(11), 1627 34. PURE AND APPLIED CHEMISTRYa
  161464. GABRIEL WEATHERHEAD
  161465. 9496N
  161466. 2/28/96V
  161467. A REVIEW.  REETZ, MANFRED T. ASYMMETRIC CARBON CARBON BOND FORMATION USING ORGANOMETALLIC CHEMISTRY. 1988, 60(11), 1607 14. PURE AND APPLIED CHEMISTRYa
  161468. GABRIEL WEATHERHEAD
  161469. 9497N
  161470. 2/28/96V
  161471. A REVIEW. MASAMUNE, SATORU. ASYMMETRIC SYNTHESIS AND ITS APPLICATIONS: TOWARD THE SYNTHESIS OF BRYOSTATIN 1. 1988 60(11), 1587 96. PURE AND APPLIED CHEMISTRYa
  161472. GABRIEL WEATHERHEAD
  161473. 9498N
  161474. 2/28/96
  161475. 9A REVIEW. UGI, IVAR K.; BAUER, JOHANNES; BAUMGARTNER, REGINA; FONTAIN, ERIC  FORSTMEYER, DIETMAR; LOHBERGER, SEVERIN. COMPUTER ASSISTANCE IN THE DESIGN OF SYNTHESIS AND A NEW GENERATION OF COMPUTER PROGRAMS FOR THE SOLUTION OF CHEMICAL PROBLEMS BY MOLECULAR LOGIC. 1988, 60(11),1573 86. PURE AND APPLIED CHEMISTRY
  161476. GABRIEL WEATHERHEAD
  161477. 9499N
  161478. 2/28/96V
  161479. A REVIEW. BARTON, DEREK H. R.; GERO, S. D.; QUICLET SIRE, B.; SAMADI, M.; OZBALIK, NUBAR; SARMA, JADAB C.; OZBALIK, N.; RAMESH, M. NEW REACTIONS FOR USE IN NATURAL PRODUCTS CHEMISTRY. 1988, 60(11), 1549 54. PURE AND APPLIED CHEMISTRYa
  161480. GABRIEL WEATHERHEAD
  161481. 9500N
  161482. 2/28/96VnA REVIEW. MEHROTRA, RAM C. CHEMISTRY OF METAL ,B DIKETONATES. 1988, 60(8), 1349 56. PURE AND APPLIED CHEMISTRYa
  161483. GABRIEL WEATHERHEAD
  161484. 9501N
  161485. 2/28/96ViA REVIEW. SIEBERT, WALTER. POLYDECKER SANDWICH COMPLEXES. 1988, 60(8), 1345 8. PURE AND APPLIED CHEMISTRYa
  161486. GABRIEL WEATHERHEAD
  161487. 9502N
  161488. 2/28/96V
  161489. A REVIEW. SHEN, QI; CHEN, WENQI; JIN, YINGTAI; SHAN, CHENGJI. SYNTHESES AND MOLECULAR STRUCTURES OF ORGANOLANTHANOIDS. 1988, 60(8), 1251 6. PURE AND APPLIED CHEMISTRYa
  161490. GABRIEL WEATHERHEAD
  161491. 9503N
  161492. 2/28/96V
  161493. A REVIEW. KAESZ, H. D.; XUE, ZILING; CHEN, YEAJER; KNOBLER, CAROLYN B.; KRONE SCHMIDT, W., SIEBER, W. J.  BOAG, N. M. REACTION OF ACETYLENES WITH EDGE DOUBLE BRIDGED TRIRUTHENIUM COMPLEXES. 1988, 60(8),1245 50. PURE AND APPLIED CHEMISTRYa
  161494. GABRIEL WEATHERHEAD
  161495. 9504N
  161496. 2/28/96V
  161497. A REVIEW. SCHULTZ, ARTHUR G. NEW PHOTOCHEMISTRY OF 2,5 CYCLOHEXADIEN L ONES AND RELATED COMPOUNDS. 1988, 60(7), 981 8. PURE AND APPLIED CHEMISTRYa
  161498. GABRIEL WEATHERHEAD
  161499. 9505N
  161500. 2/28/96V
  161501. A REVIEW. COYLE, JOHN D. ELECTRON TRANSFER PHOTOCHEMISTRY OF ORGANIC AMIDES AND IMIDES. 1988, 60(7), 941 6. PURE AND APPLIED CHEMISTRYa
  161502. GABRIEL WEATHERHEAD
  161503. 9506N
  161504. 2/28/96
  161505. A REVIEW.  ROTH, HEINZ D. MAGNETIC RESONANCE METHODS IN THE MECHANISTIC PHOTOCHEMISTRY OF KETONES, OLEFINS, AND OXIMES. 1988, 60(7), 933 40. PURE AND APPLIED CHEMISTRYa
  161506. GABRIEL WEATHERHEAD
  161507. 9507N
  161508. 2/28/96V
  161509. A REVIEW. BALCH,ALAN L. METALLOMACROCYCLES: NOVEL AMPHOTERIC MACROCYCLES WITH METAL IONS AND TRADITIONAL LEWIS BASES AS BINDING SITES. 1988, 60(4), 555 9. PURE AND APPLIED CHEMISTRYa
  161510. GABRIEL WEATHERHEAD
  161511. 9508N
  161512. 2/28/96V
  161513. A REVIEW.  GUTSCHE, C. D.  IQBAL, M.  NAM, K. S., SEE, K.; ALAM I. CONFORMATIONAL AND COMPLEXATIONAL CHARACTERISTICS OF CALIXARENES. 1988, 60(4), 483 8. PURE AND APPLIED CHEMISTRYa
  161514. GABRIEL WEATHERHEAD
  161515. 9509N
  161516. 2/28/96V
  161517. A REVIEW. STODDART, J. FRASER. CONCEPTION AND BIRTH OF NEW RECEPTOR CHEMISTRY FROM DIBENZO 18 CROWN 6. 1988, 60(4), 467 72. PURE AND APPLIED CHEMISTRYa
  161518. GABRIEL WEATHERHEAD
  161519. 9510N
  161520. 2/28/96
  161521. A REVIEW. GOKEL, GEORGE W.; ARNOLD, K. A.; DELGADO, M., ECHEVERRIA, L.; GATTO, V. J.; GUSTOWSKI, D. A.; HERNANDEZ, J.; KAIFER, A.; MILLER, S. R.; ECHEGOYEN, LUIS. LARIAT ETHERS: FROM CATION COMPLEXATION TO SUPRAMOLECULAR ASSEMBLIES. 1988 60(4), 461 5. PURE AND APPLIED CHEMISTRY
  161522. GABRIEL WEATHERHEAD
  161523. 9511N
  161524. 2/28/96V
  161525. A REVIEW.  DARENSBOURG, MARCETTA Y.; ASH, C. E.; KAO, S. C.; SILVA, R.; SPRINGS, J. MECHANISMS OF GROUP TRANSFER IN ANIONIC TRANSITION METAL HYDRIDES AND ALKYLS. 1988, 60(1),131 6. PURE AND APPLIED CHEMISTRYa
  161526. GABRIEL WEATHERHEAD
  161527. 9512N
  161528. 2/28/96V
  161529. A REVIEW. HOFFMANN, REINHARD W. A CHIRAL ALLYLBORONATES. REAGENTS FOR ASYMMETRIC SYNTHESIS. 1988, 60(1),123 30. PURE AND APPLIED CHEMISTRYa
  161530. GABRIEL WEATHERHEAD
  161531. 9513N
  161532. 2/28/96V
  161533. A REVIEW. KUWAJIMA, ISAO. L ALKOXY L SILOXYCYCLOPROPANES AS HOMOENOLATE NUCLEOPHILES OF ESTERS. 1988, 60(1) 115 22. PURE AND APPLIED CHEMISTRYa
  161534. GABRIEL WEATHERHEAD
  161535. 9514N
  161536. 2/28/96V
  161537. A REVIEW. PIERS, EDWARD. THE USE OF SOME BIFUNCTIONAL REAGENTS IN ORGANIC SYNTHESIS. 1988, 60(1),107 14. PURE AND APPLIED CHEMISTRYa
  161538. GABRIEL WEATHERHEAD
  161539. 9515N
  161540. 2/28/96V
  161541. A REVIEW. CORRIU, R. SOME ASPECTS OF THE REACTIVITY OF HYPERVALENT SPECIES OF SILICON IN ORGANIC SYNTHESIS. 1988, 60(1), 99 106. PURE AND APPLIED CHEMISTRYa
  161542. GABRIEL WEATHERHEAD
  161543. 9516N
  161544. 2/28/96V
  161545. A REVIEW. KEINAN, EHUD; EREN, DORON. TOTAL SYNTHESIS OF POLYPRENOID NATURAL PRODUCTS VIA PALLADIUM(0) CATALYZED OLIGOMERIZATIONS. 1988, 60(1), 89 98. PURE AND APPLIED CHEMISTRYa
  161546. GABRIEL WEATHERHEAD
  161547. 9517N
  161548. 2/28/96V
  161549. A REVIEW. SCHWARTZ, JEFFREY; ARVANITIS, GEORGIA M., SMEGEL, JOHN A.; MEIER, INGRID K.; CLIFT, SUSAN M.; VAN ENGEN, DONNA. NEW ORGANOMETALLIC REAGENTS FOR OLEFIN SYNTHESIS. 1988 60(1), 65 70. PURE AND APPLIED CHEMISTRYa
  161550. GABRIEL WEATHERHEAD
  161551. 9518N
  161552. 2/28/96
  161553. A REVIEW. OPPOLZER, WOLFGANG. METAL DIRECTED STEREOSELECTIVE FUNCTIONALIZATIONS OF ALKENES IN ORGANIC SYNTHESIS. 1988, 60(1), 39 48. PURE AND APPLIED CHEMISTRYa
  161554. GABRIEL WEATHERHEAD
  161555. 9519N
  161556. 2/28/96V
  161557. A REVIEW. YAMAMOTO, HISASHI, MARUOKA, KEIJI. ORGANOALUMINUM REAGENTS FOR SELECTIVE REACTIONS. 1988, 60(1), 21 6. PURE AND APPLIED CHEMISTRYa
  161558. GABRIEL WEATHERHEAD
  161559. 9520N
  161560. 2/28/96V
  161561. A REVIEW. DAVIES, STEPHEN G. ASYMMETRIC SYNTHESIS VIA THE IRON CHIRAL AUXILIARY [(ETA5 C5H5)FE(CO)(PPH3)]. 1988, 60(1), 13 20. PURE AND APPLIED CHEMISTRYa
  161562. GABRIEL WEATHERHEAD
  161563. 9521N
  161564. 2/28/96
  161565. A REVIEW. BURKHARDT, ELIZABETH R., DONEY, JEFFREY J., SLOUGH, GREG A.; STACK, JEFFREY M.; HEATHCOCK, CLAYTON H.; BERGMAN, ROBERT G. CARBON CARBON BOND FORMING REACTIONS OF ORGANOTRANSITION METAL ENOLATE COMPLEXES. 1988, 60(1),1 6. PURE AND APPLIED CHEMISTRY
  161566. GABRIEL WEATHERHEAD
  161567. 9522N
  161568. 2/28/96
  161569. A REVIEW. AKITT, J. W. MULTINUCLEAR STUDIES OF ALUMINUM COMPOUNDS. 1988, 21(1 2), 1 149. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  161570. GABRIEL WEATHERHEAD
  161571. 9523N
  161572. 2/28/96V
  161573. A REVIEW. STEPHENSON, DAVID S. LINEAR PREDICTION AND MAXIMUM ENTROPY  METHODS IN NMR SPECTROSCOPY. 1988, 20(6), PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  161574. GABRIEL WEATHERHEAD
  161575. 9524N
  161576. 2/28/96V
  161577. A REVIEW. HINTON, J. F.; METZ, K. R.; BRIGGS, R. W. THALLIUM NMR SPECTROSCOPY. 1988, 20(5), 423 513. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  161578. GABRIEL WEATHERHEAD
  161579. 9525N
  161580. 2/28/96V
  161581. A REVIEW. MURAKAMI, T.; TANAKA, N. OCCURRENCE, STRUCTURE AND TAXONOMIC IMPLICATIONS OF FERN CONSTITUENTS. 1988, 54,1 329.   PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  161582. GABRIEL WEATHERHEAD
  161583. 9526N
  161584. 2/28/96
  161585. A REVIEW. NOMURA, T. PHENOLIC COMPOUNDS OF THE MULBERRY TREE AND RELATED PLANTS. 1988, 53, 87 201. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  161586. GABRIEL WEATHERHEAD
  161587. 9527N
  161588. 2/28/96V
  161589. A REVIEW. ALVES, L. F. CHEMICAL ECOLOGY AND THE SOCIAL BEHAVIOR OF ANIMALS. 1988, 53, 1 85. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  161590. GABRIEL WEATHERHEAD
  161591. 9528N
  161592. 2/28/96V
  161593. A REVIEW. MALEK, JAROSLAV. REDUCTIONS BY METAL ALKOXYALUMINUM HYDRIDES. PART II. CARBOXYLIC ACIDS AND DERIVATIVES, NITROGEN COMPOUNDS, AND SULFUR COMPOUNDS. 1988, 36, 249 590. ORGANIC REACTIONSa
  161594. GABRIEL WEATHERHEAD
  161595. 9529N
  161596. 2/28/96V
  161597. A REVIEW. BLACK, T. HOWARD. RECENT PROGRESS IN THE CONTROL OF CARBON VERSUS OXYGEN ACYLATION OF ENOLATE ANIONS. 1988, 21(2), 179 217. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  161598. GABRIEL WEATHERHEAD
  161599. 9530N
  161600. 2/28/96
  161601. A REVIEW. LUZZIO, FREDERICK A.; GUZIEC, FRANK S., JR. RECENT APPLICATIONS OF OXOCHROMIUMAMINE COMPLEXES AS OXIDANTS IN ORGANIC SYNTHESIS. 1988, 20(6), 533 84. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  161602. GABRIEL WEATHERHEAD
  161603. 9531N
  161604. 2/28/96V
  161605. A REVIEW. RZESZOTARSKA, BARBARA, MASIUKIEWICZ, ELZBIETA. ARGININE, HISTIDINE AND TRYPTOPHAN IN PEPTIDE SYNTHESIS. THE GUANIDINO FUNCTION OF ARGININE. 1988, 20(5), 427 64. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  161606. GABRIEL WEATHERHEAD
  161607. 9532N
  161608. 2/28/96V
  161609. A REVIEW. AGUERO, ALINA; OSBORN, JOHN A. SYNTHESIS ROUTES TO METAL ALKYLIDENE COMPLEXES. 1988,12(2 3),111 18. NEW JOURNAL OF CHEMISTRYa
  161610. GABRIEL WEATHERHEAD
  161611. 9533N
  161612. 2/28/96V
  161613. A REVIEW. VORBRUEGGEN, HELMUT; MAAS, MANFRED. CARBON SUBSTITUTION OF NITROGEN HETEROCYCLES. 1988, 27(11), 2659 776. HETEROCYCLESa
  161614. GABRIEL WEATHERHEAD
  161615. 9534N
  161616. 2/28/96
  161617. A REVIEW. TOMINAGA, YOSHINORI; SHIROSHITA, YOSHIHIDE; HOSOMI, AKIRA. SYNTHESIS OF [2.2.3]CYCLAZINES, AZA[2.2.3]CYCLAZINES AND THEIR RELATED COMPOUNDS. 1988, 27(9), 2251 88. HETEROCYCLESa
  161618. GABRIEL WEATHERHEAD
  161619. 9535N
  161620. 2/28/96V
  161621. A REVIEW. SAKAMOTO, TAKAO; KONDO, YOSHINORI; YAMANAKA, HIROSHI. SYNTHESIS OF CONDENSED HETEROAROMATIC COMPOUNDS USING PALLADIUM CATALYZED REACTION. 1988, 27(9), 2225 49. HETEROCYCLESa
  161622. GABRIEL WEATHERHEAD
  161623. 9536N
  161624. 2/28/96V
  161625. A REVIEW.  CHIMIRRI, ALBA, GRASSO, SILVANA, ROMEO, GIOVANNI; ZAPPALA, MARIA. THIAZOLOBENZIMIDAZOLES. 1988, 27(8), 1975 2003. HETEROCYCLESa
  161626. GABRIEL WEATHERHEAD
  161627. 9537N
  161628. 2/28/96V
  161629. A REVIEW. TAKAHATA, HIROKI, YAMAZAKI, TAKAO. SYNTHESIS OF HETEROCYCLES USING THIOAMIDE GROUPS. 1988, 27(8), 1953 73. HETEROCYCLESa
  161630. GABRIEL WEATHERHEAD
  161631. 9538N
  161632. 2/28/96
  161633. A REVIEW. MANHAS, MAGHAR S.; WAGLE, DILIP R.; CHIANG, JUIIAN; BOSE, AJAY K. STUDIES ON LACTAMS. 79. CONVERSION OF B LACTAMS TO VERSATILE SYNTHONS VIA MOLECULAR REARRANGEMENT AND LACTAM CLEAVAGE. 1988, 27(7),1755 802. HETEROCYCLESa
  161634. GABRIEL WEATHERHEAD
  161635. 9539N
  161636. 2/28/96V
  161637. A REVIEW. NAKAYAMA, JUZO, KONISHI, TORU, HOSHINO MASAMATSU. PREPARATION OF THIOPHENE OLIGOMERS. 1988, 27(7) 1731 54. HETEROCYCLESa
  161638. GABRIEL WEATHERHEAD
  161639. 9540N
  161640. 2/28/96VyA REVIEW. RAJOPADHYE, MILIND; POPP, FRANK D. CHEMISTRY OF BENZO[B]THIOPHENE 2,3 DIONE. 1988, 27(6),1489 502. HETEROCYCLESa
  161641. GABRIEL WEATHERHEAD
  161642. 9541N
  161643. 2/28/96V
  161644. A REVIEW. IKEDA, MASAZUMI, SATO, TATSUNORI, ISHIBASHI, HIROYUKI. RECENT ADVANCES IN THE SYNTHESIS OF PYRROLIZIDINES. 1988, 27(6), 1465 87. HETEROCYCLESa
  161645. GABRIEL WEATHERHEAD
  161646. 9542N
  161647. 2/28/96
  161648. A REVIEW. SHIOIRI, TAKAYUKI, HAMADA, YASUMASA. NATURAL PRODUCT SYNTHESES UTILIZING 4 ALKOXYCARBONYLOXAZOLES AS B HYDROXY A AMINO ACID SYNTHONS. 1988, 27(4),1035 50. HETEROCYCLESa
  161649. GABRIEL WEATHERHEAD
  161650. 9543N
  161651. 2/28/96VqA REVIEW. MISLOW, K. MOLECULAR MACHINERY IN ORGANIC CHEMISTRY. 1989, 2(3), 151 174. CHEMTRACTS: ORGANIC CHEMISTRYa
  161652. GABRIEL WEATHERHEAD
  161653. 9544N
  161654. 2/28/96VsA REVIEW. WIBERG, K. B. RESONANCE INTERACTIONS IN ACYCLIC SYSTEMS. 1989, 2(2), 85 93. CHEMTRACTS: ORGANIC CHEMISTRYa
  161655. GABRIEL WEATHERHEAD
  161656. 9545N
  161657. 2/28/96V
  161658. A REVIEW. TROST, BARRY M. TRANSITION METAL TEMPLATES AS CATALYSTS FOR SELECTIVE ORGANIC TRANSFORMATIONS. 1988,1(6), 415 35. CHEMTRACTS: ORGANIC CHEMISTRYa
  161659. GABRIEL WEATHERHEAD
  161660. 9546N
  161661. 2/28/96VlA REVIEW. BROWN, HERBERT C. ASYMMETRIC SYNTHESIS MADE EASY. 1988, 1(1), 77 88. CHEMTRACTS: ORGANIC CHEMISTRYa
  161662. GABRIEL WEATHERHEAD
  161663. 9547N
  161664. 2/28/96
  161665. A REVIEW. GOLDING, BERNARD T. SYNTHESIS AND REACTIONS OF CHIRAL C3 UNITS. 1989, NO. 19, 617 21. CHEMISTRY AND INDUSTRY (LONDON)a
  161666. GABRIEL WEATHERHEAD
  161667. 9548N
  161668. 2/28/96VlA REVIEW. BROWN, JOHN M. CATALYTIC KINETIC RESOLUTION. 1988, NO. 19, 612 17. CHEMISTRY AND INDUSTRY (LONDON)a
  161669. GABRIEL WEATHERHEAD
  161670. 9549N
  161671. 2/28/96V
  161672. A REVIEW. WILD, HANNES. MODERN SYNTHETIC ROUTES TOWARDS IMPORTANT FLAVOR RAW MATERIALS. 1988, NO. 18, 580 3, 586. CHEMISTRY AND INDUSTRY (LONDON)a
  161673. GABRIEL WEATHERHEAD
  161674. 9550N
  161675. 2/28/96VdA REVIEW. PRATT, ANDREW J. ENZYMES IN ASYMMETRIC SYNTHESIS. 1989, 25(3), 282 6. CHEMISTRY IN BRITAINa
  161676. GABRIEL WEATHERHEAD
  161677. 9551N
  161678. 2/28/96VbA REVIEW. BROWN, J. M. ASYMMETRIC HOMOGENEOUS CATALYSIS. 1989, 25(3), 276 80. CHEMISTRY IN BRITAINa
  161679. GABRIEL WEATHERHEAD
  161680. 9552N
  161681. 2/28/96VZA REVIEW. DAVIES, STEPHEN G. CHIRAL AUXILIARIES. 1989, 25(3), 268 72. CHEMISTRY IN BRITAIN
  161682. GABRIEL WEATHERHEAD
  161683. 9553N
  161684. 2/28/96V
  161685. A REVIEW. DAVIES, STEPHEN G.; BROWN, JOHN M.; PRATT, ANDY, J.; FLEET, GEORGE. ASYMMETRIC SYNTHESIS
  161686. MEETING THE CHALLENGE. 1989, 25(3), 259 63. CHEMISTRY IN BRITAINa
  161687. GABRIEL WEATHERHEAD
  161688. 9554N
  161689. 2/28/96VUA REVIEW. STODDARD, FRASER. MOLECULAR LEGO. 1988, 24(12),1203 8. CHEMISTRY IN BRITAINa
  161690. GABRIEL WEATHERHEAD
  161691. 9555N
  161692. 2/28/96V~A REVIEW. BAGGOTT, JIM E. BOND SELECTIVITY: IN SEARCH OF THE CHEMISTS' DREAM. 1988, 24(9), 908 9, 911 12. CHEMISTRY IN BRITAINa
  161693. GABRIEL WEATHERHEAD
  161694. 9556N
  161695. 2/28/96VrA REVIEW. SHEPPARD, R. C. TRUE AUTOMATION OF PEPTIDE SYNTHESIS. 1988, 24(6), 557, 559, 561 2. CHEMISTRY IN BRITAINa
  161696. GABRIEL WEATHERHEAD
  161697. 9557N
  161698. 2/28/96V
  161699. A REVIEW. KERRIDGE, D. H. THE CHEMISTRY OF MOLTEN ACETAMIDE AND ACETAMIDE COMPLEXES. 1988,17(2),181 227. CHEMICAL SOCIETY REVIEWSa
  161700. GABRIEL WEATHERHEAD
  161701. 9558N
  161702. 2/28/96
  161703. VtA REVIEW. COREY, E. J. RETROSYNTHETIC THINKING ESSENTIALS AND EXAMPLES. 1988,17(2), 111 33. CHEMICAL SOCIETY REVIEWSa
  161704. GABRIEL WEATHERHEAD
  161705. 9559N
  161706. 2/28/96V]A REVIEW. BUCHANAN,G.L. THE DAKIN WEST REACTION. 1988,17(2), 91 109. CHEMICAL SOCIETY REVIEWSa
  161707. GABRIEL WEATHERHEAD
  161708. 9560N
  161709. 2/28/96V
  161710. A REVIEW. MURPHY, P. J., BRENNAN, J. THE WITTIG OLEFINATION REACTION WITH CARBONYL COMPOUNDS OTHER THAN ALDEHYDES AND KETONES. 1988,17(1), 1 30. CHEMICAL SOCIETY REVIEWSa
  161711. GABRIEL WEATHERHEAD
  161712. 9561N
  161713. 2/28/96V{A REVIEW. KEEFER, LARRY K.; LUNN, GEORGE. NICKEL ALUMINUM ALLOY AS A REDUCING AGENT. 1989, 89(3), 459 502. CHEMICAL REVIEWSa
  161714. GABRIEL WEATHERHEAD
  161715. 9562N
  161716. 2/28/96V
  161717. A REVIEW. JOHNSTON, L. J.; SCAIANO, J. C. TIME RESOLVED STUDIES OF BIRADICAL REACTIONS IN SOLUTION. 1989, 89(3), 521 47. CHEMICAL REVIEWSa
  161718. GABRIEL WEATHERHEAD
  161719. 9563N
  161720. 2/28/96
  161721. A REVIEW. PIRKLE, WILLIAM H.; POCHAPSKY, THOMAS C. CONSIDERATIONS OF CHIRAL RECOGNITION RELEVANT TO THE LIQUID CHROMATOGRAPHY SEPARATION OF ENANTIOMERS. 1989, 89(2), 347 62. CHEMICAL REVIEWSa
  161722. GABRIEL WEATHERHEAD
  161723. 9564N
  161724. 2/28/96V
  161725. A REVIEW. CONSIGLIO, GIAMBATTISTA; WAYMOUTH, ROBERT M. ENANTIOSELECTIVE HOMOGENEOUS CATALYSIS INVOLVING TRANSITIONMETAL ALLYL INTERMEDIATES. 1989, 89(1), 257 76. CHEMICAL REVIEWSa
  161726. GABRIEL WEATHERHEAD
  161727. 9565N
  161728. 2/28/96V
  161729. A REVIEW. WONG, HENRY N. C.; HON, MOON YUEN; TSE, CHUN WAH; YIP, YU CHI; TANKO, JAMES; HUDLICKY, TOMAS. USE OF CYCLOPROPANES AND THEIR DERIVATIVES IN ORGANIC SYNTHESIS. 1989, 89(1), 165 98. CHEMICAL REVIEWSa
  161730. GABRIEL WEATHERHEAD
  161731. 9566N
  161732. 2/28/96V
  161733. A REVIEW. JURCZAK, JANUSZ; GOLEBIOWSKI, ADAM. OPTICALLY ACTIVE N PROTECTED A AMINO ALDEHYDES IN ORGANIC SYNTHESIS. 1989, 89(1), 149 64. CHEMICAL REVIEWSa
  161734. GABRIEL WEATHERHEAD
  161735. 9567N
  161736. 2/28/96
  161737. A REVIEW. DUBOIS, MARY RAKOWSKI. CATALYTIC APPLICATIONS OF TRANSITION METAL COMPLEXES WITH SULFIDE LIGANDS. 1989, 89(1), 1 9. CHEMICAL REVIEWSa
  161738. GABRIEL WEATHERHEAD
  161739. 9568N
  161740. 2/28/96V
  161741. A REVIEW.  ENGELS, D. W.; UHLMANN, E. GENE SYNTHESIS. 1989, 28(6), 716 734. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161742. GABRIEL WEATHERHEAD
  161743. 9569N
  161744. 2/28/96V
  161745. A REVIEW.  CHEN, C. S.; SIH, C. J. GENERAL ASPECTS AND OPTIMIZATION OF ENANTIOSELECTIVE BIOCATALYSIS IN ORGANIC SOLVENTS: THE USE OF LIPASES. 1989, 28(6), 695 707. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161746. GABRIEL WEATHERHEAD
  161747. 9570N
  161748. 2/28/96V
  161749. A REVIEW. FABIAN, J.; ZAHRADNIK, R. THE SEARCH FOR HIGHLY COLORED ORGANIC COMPOUNDS. 1989, 28(6), 677 694. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161750. GABRIEL WEATHERHEAD
  161751. 9571N
  161752. 2/28/96
  161753. A REVIEW. DURR, H. PERSPECTIVES IN PHOTOCHROISM. A NOVEL SYSTEM BASED ON THE 1,5 ELECTROCYCLIZATION OF HETEROANALOGOUS PENTADIENYL ANIONS. 1989, 28(4), 413 431. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161754. GABRIEL WEATHERHEAD
  161755. 9572N
  161756. 2/28/96V
  161757. A REVIEW. ERKER, G. METALLOCENE CARBENE COMPLEXES AND RELATED COMPOUNDS OF TITANIUM, ZIRCONIUM AND HAFNIUM. 1989, 28(4), 397 412. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161758. GABRIEL WEATHERHEAD
  161759. 9573N
  161760. 2/28/96V
  161761. A REVIEW. BOCHE, G. THE STRUCTURE OF LITHIUM COMPOUNDS OF SULFONES, SULFOXIMIDES, SULFOXIDES, THIOETHERS, AND 1,3 DITHIANES, NITRILES, NITRO COMPOUNDS AND HYDRAZONES. 1989, 28(3), 277 297. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161762. GABRIEL WEATHERHEAD
  161763. 9574N
  161764. 2/28/96V
  161765. A REVIEW. FLOSS, H. G.; BEALE, J. M. BIOSYNTHETIC STUDIES ON ANTIBIOTICS. 1989, 28(2), 146 177. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161766. GABRIEL WEATHERHEAD
  161767. 9575N
  161768. 2/28/96V
  161769. A REVIEW. OPPOLZER, W. INTRAMOLECULAR, STOICHIOMETRIC (LI, MG, ZN) AND CATALYTIC (NI, PD, PT) METALLO ENE REACTIONS IN ORGANIC SYNTHESIS. 1989, 28(1), 38 52. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  161770. GABRIEL WEATHERHEAD
  161771. 9576N
  161772. 2/28/96V
  161773. A REVIEW. HANESSIAN, S. DESIGN AND IMPLEMENTATION OF TACTICAL NOVEL STRATEGIES FOR STEREOCHEMICAL CONTROL USING THE CHIRON APPROACH. 1989, 22(1), 3 14. ALDRICHIMICA ACTAa
  161774. GABRIEL WEATHERHEAD
  161775. 9577N
  161776. 2/28/96V
  161777. A REVIEW. LASZLO, PIERRE; CORNELIS, ANDRE. CLAY SUPPORTED CUPRIC NITRITE CLAYCOP, A USER FRIENDLY OXIDIZING AND NITRATING REAGENT. 1988, 21(4), 97 103. ALDRICHIMICA ACTAa
  161778. GABRIEL WEATHERHEAD
  161779. 9578N
  161780. 2/28/96
  161781. A REVIEW. BRUICE, THOMAS C. THE MECHANISMS OF OXYGEN TRANSFER FROM ACYL AND ALKYL HYDROPEROXIDES TO METAL(III) PORPHYRINS AND THE EPOXIDATION OF ALKENES BY THE RESULTANT HYPERVALENT METAL OXO PORPHYRIN PRODUCTS. 1989, 21(4), 87 94. ALDRICHIMICA ACTAa
  161782. GABRIEL WEATHERHEAD
  161783. 9579N
  161784. 2/28/96V
  161785. A REVIEW. IRELAND, R. E. SYNTHETIC METHODOLOGY IN THE CONTEXT OF NATURAL PRODUCT TOTAL SYNTHESIS. 1988, 21(3), 59 69. ALDRICHIMICA ACTAa
  161786. GABRIEL WEATHERHEAD
  161787. 9580N
  161788. 2/28/96VaA REVIEW. ABDULLA, RIAZ F. ULTRASOUND IN ORGANIC SYNTHESIS. 1988, 21(2), 31 42. ALDRICHIMICA ACTAa
  161789. GABRIEL WEATHERHEAD
  161790. 9581N
  161791. 2/28/96V
  161792. A REVIEW. HEWITT, CHRISTOPHER D.; SILVESTER, MICHAEL J. FLUOROAROMATIC COMPOUNDS: SYNTHESIS, REACTIONS AND COMMERCIAL APPLICATIONS. 1988, 21(1), 3 10. ALDRICHIMICA ACTAa
  161793. GABRIEL WEATHERHEAD
  161794. 9582N
  161795. 2/28/96
  161796. A REVIEW. SINNOTT, MICHAEL L. THE PRINCIPLE OF LEAST NUCLEAR MOTION AND THE THEORY OF STEREOELECTRONIC CONTROL. 1988, 24, 113 204. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  161797. GABRIEL WEATHERHEAD
  161798. 9583N
  161799. 2/28/96VqA REVIEW.  WATT, C. IAN F. HYDRIDE SHIFTS AND TRANSFERS. 1988, 24, 57 112. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  161800. GABRIEL WEATHERHEAD
  161801. 9584N
  161802. 2/28/96V}A REVIEW. NIBBERING, NICO M. M. GAS PHASE REACTIONS OF ORGANIC ANIONS. 1988, 24, 1 55. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  161803. GABRIEL WEATHERHEAD
  161804. 9585N
  161805. 2/28/96V
  161806. A REVIEW. GEOFFROY, GREGORY L.; BASSNER, SHERRI L. INTERACTION OF KETENES WITH ORGANOMETALLIC COMPOUNDS: KETENE, KETENYL, AND KETENYLIDENE COMPLEXES. 1988, 28,1 83. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  161807. GABRIEL WEATHERHEAD
  161808. 9586N
  161809. 2/28/96
  161810. A REVIEW. CHARUSHIN, V. N.; CHUPAKHIN, O. N.; VAN DER PLAS, HENK C. REACTIONS OF AZINES WITH BIFUNCTIONAL NUCLEOPHILES: CYCLIZATIONS AND RING TRANSFORMATIONS. 1988, 43, 304 53. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161811. GABRIEL WEATHERHEAD
  161812. 9587N
  161813. 2/28/96V
  161814. A REVIEW. GALLO, ROGER; ROUSSEL, CHRISTIAN; BERG, ULF. THE QUANTITATIVE ANALYSIS OF STERIC EFFECTS IN HETEROAROMATICS. 1988, 43, 173 299. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161815. GABRIEL WEATHERHEAD
  161816. 9588N
  161817. 2/28/96V
  161818. A REVIEW. GRIMMETT, M. R.; KEENE, B. R. T. REACTIONS OF ANNULAR NITROGENS OF AZINES WITH ELECTROPHILES. 1988, 43, 127 71. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161819. GABRIEL WEATHERHEAD
  161820. 9589N
  161821. 2/28/96V
  161822. A REVIEW. FLITSCH, WILHELM. HYDROGENATED PORPHYRIN DERIVATIVES: HYDROPORPHYRINS. 1988, 43, 73 126. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161823. GABRIEL WEATHERHEAD
  161824. 9590N
  161825. 2/28/96
  161826. VpA REVIEW.  FLITSCH, WILHELM. THE CHEMISTRY OF 4 AZAAZULENES. 1988, 43, 35 72. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161827. GABRIEL WEATHERHEAD
  161828. 9591N
  161829. 2/28/96VmA REVIEW.  HEWITT, DAVID. THE CHEMISTRY OF AZAPHOSPHORINS. 1988, 43, 1 34. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  161830. GABRIEL WEATHERHEAD
  161831. 9592N
  161832. 2/28/96V
  161833. A REVIEW. HOFFMAN, ROBERT V.; BARTSCH, RICHARD A.; CHO, BONG RAE. BASE PROMOTED, IMINE FORMING 1,2 ELIMINATION REACTIONS. 1989, 22(6), 211 217. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161834. GABRIEL WEATHERHEAD
  161835. 9593N
  161836. 2/28/96V
  161837. A REVIEW. ADAM, WALDEMAR; CURCI, RUGGERO; EDWARDS, J. O. DIOXIRANES: A NEW CLASS OF POWERFUL OXIDANTS. 1989, 22(6), 205 211. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161838. GABRIEL WEATHERHEAD
  161839. 9594N
  161840. 2/28/96V
  161841. A REVIEW. DOUBLEDAY, CHARLES, JR.; TURRO, NICHOLAS J.; WANG, JINFENG. DYNAMICS OF FLEXIBLE TRIPLET BIRADICALS. 1989, 22(6), 199 205. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  161842. GABRIEL WEATHERHEAD
  161843. 9595N
  161844. 2/28/96VtA REVIEW. HOLMES, ROBERT R. ORGANOTIN CLUSTER CHEMISTRY. 1989, 22(5), 190 7. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161845. GABRIEL WEATHERHEAD
  161846. 9596N
  161847. 2/28/96V
  161848. A REVIEW. JORGENSEN, WILLIAM L. FREE ENERGY CALCULATIONS: A BREAKTHROUGH FOR MODELING ORGANIC CHEMISTRY IN SOLUTION. 1989, 22(5), 184 9. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161849. GABRIEL WEATHERHEAD
  161850. 9597N
  161851. 2/28/96V
  161852. A REVIEW. COHEN, THEODORE; BHUPATHY, MAHADEVAN. ORGANOALKALI COMPOUNDS BY RADICAL ANION INDUCED REDUCTIVE METALATION OF PHENYL THIOETHERS. 1989, 22(4),152 61. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161853. GABRIEL WEATHERHEAD
  161854. 9598N
  161855. 2/28/96V
  161856. A REVIEW. WONG, HENRY N. C. SYNTHESIS OF NOVEL BENZENOID MOLECULES BY LOW VALENT TITANIUM DEOXYGENATION. 1989, 22(4),145 52. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161857. GABRIEL WEATHERHEAD
  161858. 9599N
  161859. 2/28/96
  161860. A REVIEW.  GARIN, FRANCOIS; MAIRE, GILBERT. POSSIBLE SURFACE INTERMEDIATES IN ALKANE REACTIONS ON METALLIC CATALYSTS. 1989, 22(3), 100 6. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161861. GABRIEL WEATHERHEAD
  161862. 9600N
  161863. 2/28/96V
  161864. A REVIEW. JONES, WILLIAM D.; FEHER, FRANK J. COMPARATIVE REACTIVITIES OF HYDROCARBON CARBON HYDROGEN BONDS WITH A TRANSITION METAL COMPLEX. 1989 22(3), 91 100. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161865. GABRIEL WEATHERHEAD
  161866. 9601N
  161867. 2/28/96V
  161868. A REVIEW. WAGNER, PETER J. 1,5 BIRADICALS AND FIVE MEMBERED RINGS GENERATED BY D HYDROGEN ABSTRACTION IN PHOTOEXCITED KETONES. 1989, 22(3), 83 91. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161869. GABRIEL WEATHERHEAD
  161870. 9602N
  161871. 2/28/96V
  161872. A REVIEW.  KAISER, E. T. SYNTHETIC APPROACHES TO BIOLOGICALLY ACTIVE PEPTIDES AND PROTEINS INCLUDING ENZYMES. 1989, 22(2), 47 54 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161873. GABRIEL WEATHERHEAD
  161874. 9603N
  161875. 2/28/96
  161876. A REVIEW. EFFENBERGER, FRANZ. 1,3,5 TRIS(DIALKYLAMINO)BENZENES: MODEL COMPOUNDS FOR THE ELECTROPHILIC SUBSTITUTION AND OXIDATION OF AROMATIC COMPOUNDS. 1989, 22(1), 27 35. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161877. GABRIEL WEATHERHEAD
  161878. 9604N
  161879. 2/28/96VtA REVIEW. MOSS, ROBERT A. CARBENIC REACTIVITY REVISITED. 1989, 22(1), 15 21. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161880. GABRIEL WEATHERHEAD
  161881. 9605N
  161882. 2/28/96V
  161883. A REVIEW. INGOLD, K. U.; WALTON, J. C. PROBING RING CONFORMATIONS WITH EPR SPECTROSCOPY. 1989, 22(1), 8 14. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161884. GABRIEL WEATHERHEAD
  161885. 9606N
  161886. 2/28/96V
  161887. A REVIEW. RUSSELL, GLEN A. FREE RADICAL CHAIN REACTIONS INVOLVING ALKYL  AND ALKENYLMERCURIALS. 1989, 22(1),1 8. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  161888. GABRIEL WEATHERHEAD
  161889. 9607N
  161890. 2/28/96
  161891. A REVIEW. YOSHIOKA, M. PARVEZ, S., MIYAZAKI, T., PARVEZ, H., EDS. SUPERCRITICAL FIUID CHROMATOGRAPHY AND MICRO HPLC (PROGRESS IN HPLC. VOL. 4) VSP: UTRECHT, THE NETHERLANDS, 1989.a
  161892. GABRIEL WEATHERHEAD
  161893. 9608N
  161894. 2/28/96V
  161895. A REVIEW.  VO, DINH TUAN, ED. CHEMICAL ANALYSIS OF POLYCYCLIC AROMATIC COMPOUNDS (CHEMICAL ANALYSIS, VOL. 101). WILEY: NEW YORK, 1989.a
  161896. GABRIEL WEATHERHEAD
  161897. 9609N
  161898. 2/28/96VfA REVIEW. WILLIAMS, ROBERT M. SYNTHESIS OF OPTICALLY ACTIVE AMINO ACIDS. PERGAMON: OXFORD, U.K., 1989.a
  161899. GABRIEL WEATHERHEAD
  161900. 9610N
  161901. 2/28/96V
  161902. A REVIEW. SANDLER, STANLEY R.; KARO, WOLF. ORGANIC FUNCTIONAL GROUP PREPARATION, VOLUME 3. 2ND ED. ACADEMIC PRESS: NEW YORK, 1989.a
  161903. GABRIEL WEATHERHEAD
  161904. 9611N
  161905. 2/28/96V
  161906. A REVIEW. RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOLUME 4: STEREOSELECTIVE SYNTHESIS, PART C. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1989.a
  161907. GABRIEL WEATHERHEAD
  161908. 9612N
  161909. 2/28/96V
  161910. A REVIEW.  RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOLUME 3: STEREOSELECTIVE SYNTHESIS, PART B. ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1989.a
  161911. GABRIEL WEATHERHEAD
  161912. 9613N
  161913. 2/28/96V
  161914. A REVIEW. RABIDEAU, PETER W., ED. THE CONFORMATIONAL ANALYSIS OF CYCLOHEXENES, CYCLOHEXADIENES, AND RELATED HYDROAROMATIC COMPOUNDS. VCH PUBLISHERS: NEW YORK, 1989.a
  161915. GABRIEL WEATHERHEAD
  161916. 9614N
  161917. 2/28/96V
  161918. A REVIEW.  PRETSCH, E.; CLERC, T., SEIBL, J., SIMON W. TABLES OF SPECTRAL DATA FOR STRUCTURE DETERMINATION OF ORGANIC COMPOUNDS, 2ND ED. SPRINGER: HEIDELBERG, FRG, 1989.a
  161919. GABRIEL WEATHERHEAD
  161920. 9615N
  161921. 2/28/96VjA REVIEW. PATAI, SAUL. PATAI'S GUIDE TO THE CHEMISTRY OF FUMCTIONAL GROUPS. WILEY: CHICHESTER, U.K., 1989.a
  161922. GABRIEL WEATHERHEAD
  161923. 9616N
  161924. 2/28/96
  161925. A REVIEW. PATAI, SAUL; RAPPOPORT, ZVI; EDS. THE CHEMISTRY OF ENONES, PT. 2 (THE CHEMISTRY OF FUNCTIONAL GROUPS) WILEY: CHICHESTER, U.K., 1989.a
  161926. GABRIEL WEATHERHEAD
  161927. 9617N
  161928. 2/28/96V
  161929. A REVIEW. PATAI, SAUL, RAPPOPORT, ZVI, EDS. THE CHEMISTRY OF ENONES, PT. 1 (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1989.a
  161930. GABRIEL WEATHERHEAD
  161931. 9618N
  161932. 2/28/96V}A REVIEW. PATAI, SAUL; RAPPOPORT, ZVI; EDS. THE CHEMISTRY OF ORGANIC SILICON COMPOUNDS, PT. 2. WILEY: CHICHESTER, U.K., 1989.a
  161933. GABRIEL WEATHERHEAD
  161934. 9619N
  161935. 2/28/96VwA REVIEW. PATAI, SAUL; RAPPOPORT, ZVI; EDS. THE CHEMISTRY OF ORGANIC SILICON COMPOUNDS, PT. 1. WILEY: CHICHESTER, U.K.,a
  161936. GABRIEL WEATHERHEAD
  161937. 9620N
  161938. 2/28/96V
  161939. A REVIEW.  OMAE, I. ORGANOTIN CHEMISTRY (JOURNAL OF ORGANOMETALLIC CHEMISTRY LIBRARY. 21). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1989.a
  161940. GABRIEL WEATHERHEAD
  161941. 9621N
  161942. 2/28/96
  161943. VtA REVIEW. OLAH, G. A., MALHOTRA, R., NARANG S. C. NITRATION. METHODS AND MECHANISMS. VCH PUBLISHERS: NEW YORK, 1989.a
  161944. GABRIEL WEATHERHEAD
  161945. 9622N
  161946. 2/28/96V
  161947. A REVIEW. NYIREDY, SZABOLICS, ED. OPTIMIZATION OF MOBILE PHASE. [IN: J. LIQ. CHROMATOGR.; 1989;12(1 2)]. MARCEL DEKKER: NEW YORK, 1989.a
  161948. GABRIEL WEATHERHEAD
  161949. 9623N
  161950. 2/28/96V
  161951. A REVIEW. LAZAR, MILAN; RYCHLY, JOZEF; KLIMO, VILIAM; PELIKAN, PETER; VALKO, LADISLAV. FREE RADICALS IN CHEMISTRY AND BIOLOGY. CRC PRESS: BOCA RATON, FL, 1989.a
  161952. GABRIEL WEATHERHEAD
  161953. 9624N
  161954. 2/28/96VcA REVIEW. KRSTULOVIC, A. M.; ED. CHIRAL SEPARATIONS BY HPLC. ELLIS HORWOOD: CHICHESTER, U.K., 1989.a
  161955. GABRIEL WEATHERHEAD
  161956. 9625N
  161957. 2/28/96V
  161958. A REVIEW. KOCA, J.; KRATOCHVIL, M.; KVASNICKA, V.; MATYSKA, T,.; POSPICHAL, J.  SYNTHON MODEL OF ORGANIC CHEMISTRY AND SYNTHESIS DESIGN (LECTURE NOTES IN CHEMISTRY, VOL. 51). SPRINGER VERLAG: BERLIN, FRG, 1989.a
  161959. GABRIEL WEATHERHEAD
  161960. 9626N
  161961. 2/28/96VcA REVIEW. HILL, CRAIG L., ED. ACTIVATION AND FUNCTIONALIZATION OF ALKANES. WILEY: NEW YORK, 1989. 1a
  161962. GABRIEL WEATHERHEAD
  161963. 9627N
  161964. 2/28/96V
  161965. A REVIEW. HAINES, ALAN H. METHODS FOR THE OXIDATION OF ORGANIC COMPOUNDS: ALCOHOLS, ALCOHOL DERIVATIVES, ALKYL HALIDES NITROALKANES, ALKYL AZIDES, CARBONYL COMPOUNDS, HYDROXYARENES, AND AMINOARENES. ACADEMIC PRESS: LONDON, U.K., 1988.a
  161966. GABRIEL WEATHERHEAD
  161967. 9628N
  161968. 2/28/96VlA REVIEW.  GLASS, RICHARD S., ED. CONFORMATIONAL ANALYSIS OF MEDIUM SIZED HETEROCYCLES. VCH: NEW YORK, 1988.a
  161969. GABRIEL WEATHERHEAD
  161970. 9629N
  161971. 2/28/96V
  161972. A REVIEW. FRESENIUS, PHILLIP. ORGANIC CHEMICAL NOMENCLATURE. INTRODUCTION TO THE BASIC PRINCIPLES. ELLIS HORWOOD: CHICHESTER, U.K. (TRANSLATED FROM THE GERMAN), 1989.a
  161973. GABRIEL WEATHERHEAD
  161974. 9630N
  161975. 2/28/96
  161976. A REVIEW. FISCHER, H.; HOFMANN, P.; KREISSL, F. R.; SCHROCK, R. R.; SCHUHERT, U.; WEISS, K. CARBYNE COMPLEXES. VCH: WEINHEIM, FRG, 1988.a
  161977. GABRIEL WEATHERHEAD
  161978. 9631N
  161979. 2/28/96VwA REVIEW. DUGAS, HERMANN. BIOORGANIC CHEMISTRY. A CHEMICAL APPROACH TO ENZYME ACTION, 2ND ED. SPRINGER: NEW YORK, 1989.a
  161980. GABRIEL WEATHERHEAD
  161981. 9632N
  161982. 2/28/96V
  161983. A REVIEW. DE REUCK, K. M.; ANGUS, S.; COLE, W. A.; CRAVEN, R. J. B., WAKEHAM, W. A., EDS. ETHYLENE (ETHENE). INTERNATIONAL THERMODYNAMIC TABLES OF THE FLUID STATE 10 (IUPAC). BLACKWELL: OXFORD, U.K., 1988.a
  161984. GABRIEL WEATHERHEAD
  161985. 9633N
  161986. 2/28/96V
  161987. A REVIEW. DALLAS, F. A. A.; READ, H.; RUANE, R. J.; WILSON, I. D. RECENT ADVANCES IN THIN LAYER CHROMATOGRAPHY. PLENUM: NEW YORK, 1988.a
  161988. GABRIEL WEATHERHEAD
  161989. 9634N
  161990. 2/28/96V_A REVIEW. COREY, E. J.; CHENG, XUE MIN. THE LOGIC OF CHEMICAL SYNTHESIS. WILEY: NEW YORK, 1989.a
  161991. GABRIEL WEATHERHEAD
  161992. 2/28/96VsA REVIEW. COREY, E. R.; COREY, J. Y.; GASPAR, P. P., EDS. SILICON CHEMISTRY. ELLIS HORWOOD: CHICHESTER, U.K., 1988.a
  161993. GABRIEL WEATHERHEAD
  161994. 9636N
  161995. 2/28/96V
  161996. A REVIEW. BREUER, ELI; AURICH, HANS GUENTHER; NIELSEN, ARNOLD. NITRONES, NITRONATES, AND NITROXIDES. WILEY: CHICHESTER U.K., 1989.a
  161997. GABRIEL WEATHERHEAD
  161998. 9637N
  161999. 2/28/96V}A REVIEW. ATHERTON, E., SHEPPARD, R. C. SOLID PHASE PEPTIDE SYNTHESIS. IRL PRESS/OXFORD UNIVERSITY PRESS: OXFORD, U.K., 1989.a
  162000. GABRIEL WEATHERHEAD
  162001. 9638N
  162002. 2/28/96V
  162003. A REVIEW. AGRAWAL, P. K., ED. CARBON 13 NMR OF FLAVONOIDS (STUDIES IN ORGANIC CHEMISTRY. VOL. 39). ELSEVIER: AMSTERDAM, THE NETHERLANDS, 1989.a
  162004. GABRIEL WEATHERHEAD
  162005. 9639N
  162006. 2/28/96V
  162007. A REVIEW. ROBERTS, S. M. BIOTRANSFORMATIONS RELATING TO HETEROCYCLIC COMPOUNDS. PROGRESS IN HETEROCYCLIC CHEMISTRY. VOLUME 1, H. SUSCHITZKY AND E. F. V. SCRIVEN, EDS., PERGAMON PRESS, OXFORD, U.K., 1989.a
  162008. GABRIEL WEATHERHEAD
  162009. 9640N
  162010. 2/28/96V
  162011. A REVIEW. BOGER, D. L., PATEL, M. RECENT APPLICATIONS OF THE INVERSE ELECTRON DEMAND DIELS ALDER REACTION. PROGRESS IN HETEROCYCLIC CHEMISTRY. VOLUME 1, H. SUSCHITZKY AND E. F. V. SCRIVEN, EDS., PERGAMON PRESS, OXFORD, U.K., 1989.a
  162012. GABRIEL WEATHERHEAD
  162013. 9641N
  162014. 2/28/96
  162015. A REVIEW. KATRITZKY, A. R., LAM J. N., SENGUPTA, S., REWCASTLE G. W. SOME NEW STRATEGIES FOR PROTECTION, ACTIVATION AN DIRECTION IN LITHIATION CHEMISTRY. PROGRESS IN HETEROCYCLIC CHEMISTRY. VOLUME 1, H. SUSCHITZKY AND E. F. V. SCRIVEN, EDS., PERGAMON PRESS, OXFORD, U.K., 1989.
  162016. GABRIEL WEATHERHEAD
  162017. 9642N
  162018. 2/28/96V
  162019. A REVIEW. MAJETICH, GEORGE. ALLYLSILANES IN ORGANIC SYNTHESIS. ORGANIC SYNTHESIS: THEORY AND APPLICATIONS. VOLUME 1, TOMAS HUDLICKY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162020. GABRIEL WEATHERHEAD
  162021. 9643N
  162022. 2/28/96
  162023. A REVIEW. GIGUERE, RAYMOND J. NONCONVENTIONAL REACTION CONDITIONS: ULTRASOUND, HIGH PRESSURE, AND MICROWAVE HEATING IN ORGANIC SYNTHESIS. ORGANIC SYNTHESIS: THEORY AND APPLICATIONS. VOLUME 1, TOMAS HUDLICKY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162024. GABRIEL WEATHERHEAD
  162025. 9644N
  162026. 2/28/96V
  162027. A REVIEW. TASHNER, MICHAEL J. ASYMMETRIC DIELS ALDER REACTIONS. ORGANIC SYNTHESIS: THEORY AND APPLICATIONS. VOLUME 1, TOMAS HUDLICKY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162028. GABRIEL WEATHERHEAD
  162029. 9645N
  162030. 2/28/96V
  162031. A REVIEW. JOHNSON, RICHARD P. CYCLIC CUMULENES. ADVANCES IN THEORETICALLY INTERESTING MOLECULES. VOLUME 1, RANDOLPH P. THUMMEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162032. GABRIEL WEATHERHEAD
  162033. 9646N
  162034. 2/28/96
  162035. A REVIEW. MARCHAND, ALAN P. THE CHEMISTRY OF PENTACYCLO(5.4.0.02,6. 03,10. 05,9) UNDECANE (PCUD) AND RELATED SYSTEMS. ADVANCES IN THEORETICALLY INTERESTING MOLECULES. VOLUME 1, RANDOLPH P. THUMMEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162036. GABRIEL WEATHERHEAD
  162037. 9647N
  162038. 2/28/96V
  162039. A REVIEW. VOGEL, PIERRE. (1.M.N)HERICENES AND RELATED EXOCYCLIC POLYENES. ADVANCES IN THEORETICALLY INTERESTING MOLECULES. VOLUME 1, RANDOLPH P. THUMMEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162040. GABRIEL WEATHERHEAD
  162041. 9648N
  162042. 2/28/96V
  162043. A REVIEW. MITCHELL, REGINALD H. DIHYDROPYRENES: BRIDGED (14) ANNULENES PAR EXCELLENCE. A COMPARISON WITH OTHER BRIDGED ANNULENES. ADVANCES IN THEORETICALLY INTERESTING MOLECULES. VOLUME 1, RANDOLPH P. THUMMEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162044. GABRIEL WEATHERHEAD
  162045. 9649N
  162046. 2/28/96
  162047. A REVIEW. RICKBORN, BRUCE. ISOBENZOFURANS. ADVANCES IN THEORETICALLY INTERESTING MOLECULES. VOLUME 1, RANDOLPH P. THUMMEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162048. GABRIEL WEATHERHEAD
  162049. 9650N
  162050. 2/28/96V
  162051. A REVIEW. WULFF, WILLIAM D. TRANSITION METAL CARBENE COMPLEXES IN ORGANIC SYNTHESIS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162052. GABRIEL WEATHERHEAD
  162053. 9651N
  162054. 2/28/96V
  162055. A REVIEW. NEGISHI, EI ICHI. METAL ORGANIC APPROACH TO STEREOSELECTIVE SYNTHESIS OF EXOCYCLIC ALKENES. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162056. GABRIEL WEATHERHEAD
  162057. 9652N
  162058. 2/28/96V
  162059. A REVIEW. BACKVALL, JAN E. METAL MEDIATED ADDITIONS TO CONJUGATED DIENES. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162060. GABRIEL WEATHERHEAD
  162061. 2/28/96V
  162062. A REVIEW. SOLLADIE CAVALLO, ARLETTE. CHIRAL ARENE CHROMIUM CARBONYL COMPLEXES IN ASYMMETRIC SYNTHESIS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162063. GABRIEL WEATHERHEAD
  162064. 9654N
  162065. 2/28/96V
  162066. A REVIEW. OJIMA, IWAO. NEW CARBONYLATIONS BY MEANS OF TRANSITION METAL CATALYSTS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162067. GABRIEL WEATHERHEAD
  162068. 9655N
  162069. 2/28/96V
  162070. A REVIEW. PEARSON, ANTHONY J. RECENT DEVELOPMENTS IN THE SYNTHETIC APPLICATIONS OF ORGANOIRON AND ORGANOMOLYBDENUM CHEMISTRY. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 1, LANNY S. LIEBESKIND, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162071. GABRIEL WEATHERHEAD
  162072. 9656N
  162073. 2/28/96VkA REVIEW. WONG ET AL., HETEROCYCLES., 26, 1345 (1987). STEREOSPECIFIC DEOXYGENATION OF EPOXIDES TO OLEFINS.a
  162074. GABRIEL WEATHERHEAD
  162075. 2/28/96V
  162076. A REVIEW. G. MAAS, TOP. CURR. CHEM., 137, 75 (1987). TRANSITION METAL CATALYZED DECOMPOSITION OF ALPHATIC DIAZO COMPOUNDS   NEW RESULTS AND APPLICATIONS IN ORGANIC SYNTHESIS .a
  162077. GABRIEL WEATHERHEAD
  162078. 9658N
  162079. 2/28/96V[A REVIEW. M. RAMAIAH, TETRAHEDRON, 43, 3541 (1987). RADICAL REACTIONS IN ORGANIC SYNTHESIS.a
  162080. GABRIEL WEATHERHEAD
  162081. 9659N
  162082. 2/28/96V
  162083. A REVIEW. D. CRICH, ALDRICHIMICA ACTA, 20, 35 (1987). O ACYLTHIOHYDROXAMATES : NEW AND VERSATILE SOURCES OF ALKYL RADICALS FOR USE IN ORGANIC SYNTHESIS.a
  162084. GABRIEL WEATHERHEAD
  162085. 9660N
  162086. 2/28/96V
  162087. A REVIEW. R.W. HOFFMANN, D. HOPPE ET AL., ANGEW. CHEM., INT. ED. ENGL., 26, 1145 (1987). ESTIMATION OF THE CONFIGURATIONAL STABILITY OF CHIRAL ORGANOMETALLIC REAGENTS.a
  162088. GABRIEL WEATHERHEAD
  162089. 9661N
  162090. 2/28/96
  162091. A REVIEW. A.A. SOLOV'YANOV AND I.P. BELETSKAYA, RUSS. CHEM. REV., 56, 465 (1987). REACTIONS OF CARBONYL COMPOUNDS WITH ORGANIC DERIVATIVES OF ALKALI METALS AND HYDRIDE REDUCTANTS: THE EFFECTS OF THE MEDIUM AND THE CATION.a
  162092. GABRIEL WEATHERHEAD
  162093. 9662N
  162094. 2/28/96VeA REVIEW. E. ERDIK, TETRAHEDRON, 43, 2203 (1987). USE OF ACTIVATION METHODS FOR ORGANOZINC REAGENTS .a
  162095. GABRIEL WEATHERHEAD
  162096. 9663N
  162097. 2/28/96V
  162098. A REVIEW. S.J. BLUNDEN, P.A. CUSACK AND P.J. SMITH, J. ORGANOMET. CHEM., 325, 141 (1987). THE USE OF TIN COMPOUNDS IN CARBOHYDRATE AND NUCLEOSIDE CHEMISTRYa
  162099. GABRIEL WEATHERHEAD
  162100. 9664N
  162101. 2/28/96VtA REVIEW. H. TAKAKU, J. SYNTH. ORG. CHEM. JPN., 45, L96 (1987) RECENT DEVELOPMENTS IN PHOSPHORYLATION OF NUCLEOSIDESa
  162102. GABRIEL WEATHERHEAD
  162103. 9665N
  162104. 2/28/96
  162105. A REVIEW. S.G. DAVIES ET AL., BULL SOC. CHIM. FR., 608 (1987). SYNTHESIS AND STEREOSELECTIVE REACTIONS OF A,B UNSATURATED ACYL LIGANDS BOUND TO THE CHIRAL AUXILIARY (ETA5 C5H5)FE(CO)(PPH3)a
  162106. GABRIEL WEATHERHEAD
  162107. 9666N
  162108. 2/28/96V
  162109. A REVIEW. W. OPPOLZER, TETRAHEDRON, 43, 1969 (1987). TETRAHEDRON REPORT 216: CAMPHOR DERIVATIVES AS CHIRAL AUXILIARIES IN ASYMMETRIC SYNTHESISa
  162110. GABRIEL WEATHERHEAD
  162111. 9667N
  162112. 2/28/96V
  162113. A REVIEW. G.H. POSNER, ACC.CHEM. RES., 20, 72 (1987). ASYMMETRIC SYNTHESIS OF CARBON CARBON BONDS USING SULFINYL CYCLOALKENONES, ALKENOLIDES AND PYRONESa
  162114. GABRIEL WEATHERHEAD
  162115. 9668N
  162116. 2/28/96V
  162117. A REVIEW. M. SREBNIK AND P.V. RAMACHANDRAN, ALDRICHIMICA ACTA, 20, 9 (1987 ) . THE UTILITY OF CHIRAL ORGANOBORANES IN THE PREPARATION OF OPTICALLY ACTIVE COMPOUNDSa
  162118. GABRIEL WEATHERHEAD
  162119. 9669N
  162120. 2/28/96
  162121. A REVIEW. S. ITSUNO, J. SYNTH. ORG. CHEM. JPN., 45, 101 (1987). CATALYTIC ASYMMETRIC REDUCTION USING OPTICALLY ACTIVE AMINO ALCOHOL BORANE COMPLEXa
  162122. GABRIEL WEATHERHEAD
  162123. 9670N
  162124. 2/28/96V
  162125. A REVIEW. M. BROOKHART AND W.B. STUDABAKER, CHEM. REV., 87 411 (1987). CYCLOPROPANES FROM REACTIONS OF TRANSITION  METAL CARBENE COMPLEXES WITH OLEFINSa
  162126. GABRIEL WEATHERHEAD
  162127. 9671N
  162128. 2/28/96V
  162129. A REVIEW. D. LLOYD, I. GOSNEY AND R.A. ORMISTON, CHEM. SOC. REV., 16, 45 (1987). ARSONIUM YLIDES (WITH SOME MENTION ALSO OF ARSINIMINES, STIBONIUM AND BISMUTHONIUM YLIDES)a
  162130. GABRIEL WEATHERHEAD
  162131. 9672N
  162132. 2/28/96V
  162133. A REVIEW. L. EBERSON AND F. RADNER, ACC. CHEM. RES., 20, 53 (1987). ELECTRON TRANSFER MECHANISMS IN ELECTROPHILIC AROMATIC NITRATIONa
  162134. GABRIEL WEATHERHEAD
  162135. 9673N
  162136. 2/28/96VvA REVIEW. A.L. CAMPBELL AND G.R. LENZ, SYNTHESIS, 421 (1987). THE GROUND STATE AND EXCITED STATE REACTIONS OF ENAMIDESa
  162137. GABRIEL WEATHERHEAD
  162138. 9674N
  162139. 2/28/96VaA REVIEW. N.L. BAULD ET AL., ACC. CHEM. RES., 20, 371 (1987). CATION RADICAL PERICYCLIC REACTIONSa
  162140. GABRIEL WEATHERHEAD
  162141. 9675N
  162142. 2/28/96VgA REVIEW. J.L. COURTNEIDGE AND A.G. DAVIES, ACC. CHEM. RES., 20, 90 (1987). HYDROCARBON RADICAL CATIONSa
  162143. GABRIEL WEATHERHEAD
  162144. 9676N
  162145. 2/28/96V
  162146. A REVIEW. H.D. ROTH, ACC. CHEM. RES., 20, 343 (1987). ORGANIC RADICAL CATIONS IN FLUID SOLUTION: UNUSUAL STRUCTURES AND REARRANGEMENTSa
  162147. GABRIEL WEATHERHEAD
  162148. 9677N
  162149. 2/28/96V
  162150. A REVIEW. E.T. DENISOV AND I.V. KHUDYAKOV, CHEM. REV., 87, 1313 (1987) MECHANISMS OF ACTION AND REACTIVITIES OF THE FREE RADICALS OF INHIBITORSa
  162151. GABRIEL WEATHERHEAD
  162152. 9678N
  162153. 2/28/96VtA REVIEW. J. MATTAY, ANGEW. CHEM. INT. ED. ENGL., 26, 825 (1987). CHARGE TRANSFER AND RADICAL IONS IN PHOTOCHEMISTRYa
  162154. GABRIEL WEATHERHEAD
  162155. 9679N
  162156. 2/28/96
  162157. A REVIEW. D. CRICH, ALDRICHIMICA ACTA, 20, 35 (1987). O ACYL THIOHYDROXAMATES: NEW AND VERSATILE SOURCES OF ALKYL RADICALS FOR USE IN ORGANIC SYNTHESISa
  162158. GABRIEL WEATHERHEAD
  162159. 9680N
  162160. 2/28/96VrA REVIEW. M. RAMAIAH, TETRAHEDRON, 43, 3541 (1987). TETRAHEDRON REPORT 223: RADICAL REACTIONS IN ORGANIC SYNTHESISa
  162161. GABRIEL WEATHERHEAD
  162162. 9681N
  162163. 2/28/96VzA REVIEW. S. CHANDRASEKHAR, CHEM. SOC. REV., 16, 313 (1987). PRODUCT STABILITY IN KINETICALLY CONTROLLED ORGANIC REACTIONSa
  162164. GABRIEL WEATHERHEAD
  162165. 9682N
  162166. 2/28/96V~A REVIEW. G. L'ABBE, SYNTHESIS, 525 (1987). SIX MEMBERED HETEROCYCLIC ISOCYANATES AND ISOTHIOCYANATES: SYNTHESIS AND REACTIONSa
  162167. GABRIEL WEATHERHEAD
  162168. 9683N
  162169. 2/28/96VYA REVIEW. D.W. ROBERTS AND D.L. WILLIAMS, TETRAHEDRON, 43, 1027 (1987). SULTONE CHEMISTRYa
  162170. GABRIEL WEATHERHEAD
  162171. 9684N
  162172. 2/28/96
  162173. A REVIEW. A.A. MARTIN AND G. BARNIKOW, Z. CHEM., 27, 90 (1987). THIOCARBOXYLIC ANHYDRIDES    A NEW CLASS OF THIOACYLATING REAGENTSa
  162174. GABRIEL WEATHERHEAD
  162175. 9685N
  162176. 2/28/96V
  162177. A REVIEW. M. EVERS, CHEMICA SCRIPTA, 26, 585 (1986). ALKANE THIOLATE AND SELENOLATE ANIONS: USEFUL REAGENTS FOR THE CLEAVAGE OF THE ALKYL CHALCOGEN BOND OF ALKYL ARYL CHALCOGENIDESa
  162178. GABRIEL WEATHERHEAD
  162179. 9686N
  162180. 2/28/96V
  162181. A REVIEW. J. LIEBSCHER, A. KNOLL AND B. ABEGAS, Z. CHEM., 27, 8 (1987). CHEMISTRY OF THE 3 AMINOTHIOACRYLAMIDES   SYNTHESES AND PROPERTIESa
  162182. GABRIEL WEATHERHEAD
  162183. 9687N
  162184. 2/28/96V
  162185. A REVIEW. V.M. DZHEMILEV ET AL., RUSS. CHEM. REV., 56, 36 (1987). NORBORNADIENES IN THE SYNTHESIS OF POLYCYCLIC STRAINED HYDROCARBONS WITH PARTICIPATION OF METAL COMPLEX CATALYSTSa
  162186. GABRIEL WEATHERHEAD
  162187. 9688N
  162188. 2/28/96VWA REVIEW. D. GINSBURG, TOP. CURR.CHEM., 137, 1 (1987). OF PROPELLANES    AND OF SPIRANSa
  162189. GABRIEL WEATHERHEAD
  162190. 9689N
  162191. 2/28/96V
  162192. A REVIEW. L.A. PAVLOVA ET AL., RUSS. CHEM. REV., 55, 1026 (1986). ALKYL ORTHOESTERS AND THEIR APPLICATIONS IN ORGANIC SYNTHESISa
  162193. GABRIEL WEATHERHEAD
  162194. 9690N
  162195. 2/28/96VkA REVIEW. M.G. VINOGRADOV ET AL., RUSS. CHEM. REV., 55, 1130 (1986). OXALLYL COMPLEXES IN ORGANIC SYNTHESISa
  162196. GABRIEL WEATHERHEAD
  162197. 9691N
  162198. 2/28/96V
  162199. A REVIEW. U. PINDUR ET AL., CHEM. SOC. REV., 16, 75 (1987). ORTHO ESTERS AND DIALKOXYCARBENIUM IONS: REACTIVITY, STABILITY, STRUCTURE AND NEW SYNTHETIC APPLICATIONSa
  162200. GABRIEL WEATHERHEAD
  162201. 9692N
  162202. 2/28/96VeA REVIEW. G.R.KROW, TETRAHEDRON, 43, 3 (1987). ONE CARBON RING EXPANSIONS OF BRIDGED BICYCLIC KETONESa
  162203. GABRIEL WEATHERHEAD
  162204. 9693N
  162205. 2/28/96V
  162206. A REVIEW. H. HARTMANN AND D. KLEMM, Z. CHEM., 27, 1 (1987). BIOLOGICALLY ACTIVE FUNCTIONALIZATION OF MACROMOLECULAR ORGANIC COMPOUNDSa
  162207. GABRIEL WEATHERHEAD
  162208. 9694N
  162209. 2/28/96
  162210. A REVIEW. N. CELEBI, FABAD FARM. BIL. DER., 12, 5 (1987). CYCLODEXTRINS. I. PROPERTIES, METHODS OF PREPARATION AND THEIR CLATHRATE COMPOUNDSa
  162211. GABRIEL WEATHERHEAD
  162212. 9695N
  162213. 2/28/96VuA REVIEW. A.W. FRANK, PHOSPHORUS AND SULPHUR, 29, 297 (1987). NON ENZYMIC METHODS FOR THE PHOSPHORYLATION OF PROTEINSa
  162214. GABRIEL WEATHERHEAD
  162215. 9696N
  162216. 2/28/96VaA REVIEW. R. NOACK AND K. SCHWETLICK, Z. CHEM., 27, 77 (1987). INSERTION REACTIONS OF ISOCYANATESa
  162217. GABRIEL WEATHERHEAD
  162218. 9697N
  162219. 2/28/96ViA REVIEW. T. MUKAIYAMA AND M. MURAKAMI, SYNTHESIS, 1043 (1987). CROSS COUPLING REACTIONS BASED ON ACETALSa
  162220. GABRIEL WEATHERHEAD
  162221. 9698N
  162222. 2/28/96VmA REVIEW. M. CHANON, ACC. CHEM. RES., 20, 214 (1987). ELECTRON TRANSFER INDUCED CHAIN REACTIONS AND CATALYSISa
  162223. GABRIEL WEATHERHEAD
  162224. 9699N
  162225. 2/28/96VwA REVIEW. N.S. ZEFIROV, ACC. CHEM. RES., 20, 237 (1987). AN APPROACH TO SYSTEMATIZATION AND DESIGN OF ORGANIC REACTIONS
  162226. GABRIEL WEATHERHEAD
  162227. 9700N
  162228. 2/28/96V
  162229. A REVIEW. A. KAJI, R. TANIKAGA, K. TANAKA AND N. ONO, J. SYNTH. ORG. CHEM., JPN., 45, 421 (1987). STUDIES ON THE DEVELOPMENT OF NEW REACTIONS FOR ORGANIC SYNTHESIS. SYNTHETIC REACTIONS USING ORGANIC SULPHUR AND NITRO COMPOUNDSa
  162230. GABRIEL WEATHERHEAD
  162231. 9701N
  162232. 2/28/96VwA REVIEW. M. MAKOSZA AND J. WINIARSKI, ACC. CHEM. RES., 20, 282 (1987). VICARIOUS NUCLEOPHILIC SUBSTITUTION OF HYDROGENa
  162233. GABRIEL WEATHERHEAD
  162234. 9702N
  162235. 2/28/96V
  162236. A REVIEW. M.L. PETROV AND A.A. PETROV, RUSS. CHEM. REV., 56, 152 (1987). THE 1,3 ANIONIC CYCLOADDITION REACTIONS OF A,B UNSATURATED THIOLATES AND THEIR ANALOGSa
  162237. GABRIEL WEATHERHEAD
  162238. 9703N
  162239. 2/28/96VvA REVIEW. J.L. CHARLTON AND M.M. ALAUDDIN, TETRAHEDRON, 43, 2873 (1987). TETRAHEDRON REPORT 220: ORTHO QUINODIMETHANESa
  162240. GABRIEL WEATHERHEAD
  162241. 9704N
  162242. 2/28/96
  162243. lVvA REVIEW. D. CRAIG, CHEM. SOC. REV., 16, 187 (1987). STEREOCHEMICAL ASPECTS OF THE INTRAMOLECULAR DIELS ALDER REACTIONa
  162244. GABRIEL WEATHERHEAD
  162245. 9705N
  162246. 2/28/96VeA REVIEW. A. ICHIHARA, SYNTHESIS, 207 (1987). RETRO DIELS ALDER STRATEGY IN NATURAL PRODUCT SYNTHESISa
  162247. GABRIEL WEATHERHEAD
  162248. 9706N
  162249. 2/28/96V
  162250. A REVIEW. A.J. FATIADI, SYNTHESIS, 749 (1987). ADDITION AND CYCLOADDITION REACTIONS OF TETRACYANOETHYLENE (TCNE) IN ORGANIC CHEMISTRYa
  162251. GABRIEL WEATHERHEAD
  162252. 9707N
  162253. 2/28/96V
  162254. A REVIEW. M. BRAUN, ANGEW. CHEM. INT. ED. ENGL., 26, 24 (1987). STEREOSELECTIVE ALDOL REACTIONS WITH A UNSUBSTITUTED CHIRAL ENOLATESa
  162255. GABRIEL WEATHERHEAD
  162256. 9708N
  162257. 2/28/96V
  162258. A REVIEW. H.N.C. WONG, C.C.M. FOK AND T. WONG, HETEROCYCLES, 26, 1345 (1987). STEREOSPECIFIC DEOXYGENATION OF EPOXIDES TO OLEFINSa
  162259. GABRIEL WEATHERHEAD
  162260. 9709N
  162261. 2/28/96
  162262. A REVIEW. K. FURUHASHI, J. SYNTH. ORG. CHEM., JPN., 45, 162 (1987). PRODUCTION OF OPTICALLY ACTIVE EPOXIDES BY MICROBIAL OXIDATION OF OLEFINSa
  162263. GABRIEL WEATHERHEAD
  162264. 9710N
  162265. 2/28/96VpA REVIEW. T. KATSUKI, J. SYNTH. ORG. CHEM., JPN., 45, 90 (1987). ''RECENT DEVELOPMENTS IN ASYMMETRIC EPOXIDATIONa
  162266. GABRIEL WEATHERHEAD
  162267. 9711N
  162268. 2/28/96V
  162269. A REVIEW. H. BRUNNER AND H. LEYERER, BULL. SOC. CHIM. BELG., 96, 353 (1987). METHYLBUTYLPHOSPHINES AND THEIR RHODIUM COMPLEXES    ENANTIOSELECTIVE CATALYSTSa
  162270. GABRIEL WEATHERHEAD
  162271. 9712N
  162272. 2/28/96VlA REVIEW. F. TODA, J. SYNTH. ORG. CHEM., JPN., 45, 745 (1987). OPTICAL RESOLUTION BY HOST GUEST COMPLEXATIONa
  162273. GABRIEL WEATHERHEAD
  162274. 9713N
  162275. 2/28/96V
  162276. A REVIEW. L.A. CARPINO, ACC. CHEM. RES., 20, 401 (1987). THE 9 FLUOROENYLMETHOYLOXYCARBONYL FAMILY OF BASE SENSITIVE AMINO PROTECTING GROUPSa
  162277. GABRIEL WEATHERHEAD
  162278. 9714N
  162279. 2/28/96
  162280. A REVIEW. K. TROEV AND G. BORISOV, PHOSPHORUS AND SULPHUR, 29, 129 (1987). CHARACTERISTIC REACTIONS OF THE ALKOXY GROUPS OF THE ACID DIESTERS OF PHOSPHORUS ACIDa
  162281. GABRIEL WEATHERHEAD
  162282. 9715N
  162283. 2/28/96VoA REVIEW. U. HACKSELL AND T. HOGBERG, ACTA PHARM. SUECICA, 23, 6 (1986). PROTECTIVE GROUPS IN ORGANIC SYNTHESISa
  162284. GABRIEL WEATHERHEAD
  162285. 9716N
  162286. 2/28/96V~A REVIEW. B.Y. RIAD, A.M. NEGM, S.E. ABDOU AND H.A. DABOUN, HETROCYCLES, 26, 205 (1987). THE CHEMISTRY OF A CYANOTHIOACETAMIDEa
  162287. GABRIEL WEATHERHEAD
  162288. 9717N
  162289. 2/28/96V
  162290. A REVIEW. M.H. ELNAGDI, S.M. SHERIF AND R.M. MOHAREB, HETEROCYCLES, 26, 497 (1987). THE SYNTHETIC POTENTIALITIES OF NITRILES IN HETEROCYCLIC SYNTHESISa
  162291. GABRIEL WEATHERHEAD
  162292. 9718N
  162293. 2/28/96V
  162294. A REVIEW. S. EGUCHI, T. OKANO AND H. TAKEUCHI, HETEROCYCLES, 26, 3265 (1987). SYNTHESIS OF AZAMODIFIED ADAMANTANE DERIVATIVES VIA BRIDGEHEAD AND BRIDGE IMINESa
  162295. GABRIEL WEATHERHEAD
  162296. 9719N
  162297. 2/28/96V
  162298. A REVIEW. R. GRIGG, CHEM. SOC. REV., 16, 89 (1987). PROTOTROPIC ROUTES TO 1,3  AND 1,5 DIPOLES AND 1,2 YLIDES: APPLICATIONS TO THE SYNTHESIS OF HETEROCYCLIC COMPOUNDSa
  162299. GABRIEL WEATHERHEAD
  162300. 9720N
  162301. 2/28/96V
  162302. A REVIEW. L.D. FREEDMAN AND H.S. FREEMAN, CHEM. REV., 87, Z89 (1987). PREPARATION, REACTIONS, STRUCTURES AND POSSIBLE USES OF 5,10 DIHYDROPHENOPHOSPHAZINE DERIVATIVESa
  162303. GABRIEL WEATHERHEAD
  162304. 9721N
  162305. 2/28/96V
  162306. A REVIEW. C.K. BRADSHER, CHEM. REV., 87, 1277 (1987). FORMATION OF SIX MEMBERED AROMATIC RINGS BY CYCLIALKYLATION OF SOME ALDEHYDES AND KETONESa
  162307. GABRIEL WEATHERHEAD
  162308. 9722N
  162309. 2/28/96VmA REVIEW. T. OHMAYE, J. SYNTH. ORG. CHEM. JPN., 45, 691 (1987). REVIEW ON SYNTHETIC METHODS FOR VINYL ACETATEa
  162310. GABRIEL WEATHERHEAD
  162311. 9723N
  162312. 2/28/96V{A REVIEW. G.R. NEWKOME AND G.R. BAKER, ORG. PREP. PROCED. INT., 8, 117 (1986). THE CHEMISTRY OF METHANETRICARBOXYLIC ESTERSa
  162313. GABRIEL WEATHERHEAD
  162314. 9724N
  162315. 2/28/96VzA REVIEW. G. KRESZE, B. ASCHERL, H. BRAUN AND H. FELBER, ORG. PREP. PROCED. INTL., 19, 329 (1987). A HALONITROSO COMPOUNDSa
  162316. GABRIEL WEATHERHEAD
  162317. 9725N
  162318. 2/28/96V
  162319. A REVIEW. J.E. SAAVEDRA, ORG. PREP. PROCED. INTL., 19, 83 (1987). RECENT SYNTHETIC APPLICATIONS OF N NITROSAMINES AND RELATED COMPOUNDSa
  162320. GABRIEL WEATHERHEAD
  162321. 9726N
  162322. 2/28/96V
  162323. A REVIEW. J.S. SANDHU AND B. SAIN, HETEROCYCLES, 26, 777 (1987). SOME RECENT ADVANCES IN THE CHEMISTRY OF IMINES, IN PARTICULAR CYCLOADDITION REACTIONSa
  162324. GABRIEL WEATHERHEAD
  162325. 9727N
  162326. 2/28/96VsA REVIEW. W. CARRUTHERS, PERGAMON PRESS, ORGANIC CHEMISTRY VOL.7. BOOK: CYCLOADDITION REACTIONS IN ORGANIC SYNTHSISa
  162327. GABRIEL WEATHERHEAD
  162328. 9728N
  162329. 2/28/96V
  162330. A REVIEW. V. RAMAMURTHY, J.R. SCHEFFER AND N.J. TURRO, TETRAHEDRON, 43, 1197 (1987). SYMPOSIUM IN PRINT 29: ORGANIC CHEMISTRY IN ANISOTROPIC MEDIAa
  162331. GABRIEL WEATHERHEAD
  162332. 9729N
  162333. 2/28/96V
  162334. A REVIEW. R.W. HOFFMANN, ANGEW. CHEM. INT. ED. ENGL., 26, 489 (1987). STEREOSELECTIVE SYNTHESES OF BUILDING BLOCKS WITH THREE CONSECUTIVE STEREOGENIC CENTERS: IMPORTANT PRECURSORS OF POLYKETIDE NATURAL PRODUCTSa
  162335. GABRIEL WEATHERHEAD
  162336. 9730N
  162337. 2/28/96V
  162338. A REVIEW. H. KUNZ, ANGEW. CHEM. INT. ED. ENGL., 26, 294 (1987). SYNTHESIS OF GLYCOPEPTIDES, PARTIAL STRUCTURES OF BIOLOGICAL RECOGNITION COMPONENTSa
  162339. GABRIEL WEATHERHEAD
  162340. 9731N
  162341. 2/28/96V~A REVIEW. B.S. JOSHI AND S.W. PELLETIER, HETEROCYCLES, 26, 2503 (1987). X RAY CRYSTAL STRUCTURES OF C L9 DITERPENOID ALKALOIDSa
  162342. GABRIEL WEATHERHEAD
  162343. 9732N
  162344. 2/28/96V
  162345. A REVIEW. F. PIOZZI, B. RODRIGUEZ AND G. SAVONA, HETEROCYCLES, 25, 807 (1987). ADVANCES IN THE CHEMISTRY OF THE FURANODITERPENOIDS FROM TEUCRIUM SPECIESa
  162346. GABRIEL WEATHERHEAD
  162347. 9733N
  162348. 2/28/96
  162349. VyA REVIEW. V.H. RAWAL, R.J. JONES AND M.P. CAVA, HETEROCYCLES, 25, 701 (1987). SYNTHETIC STUDIES TOWARD CC 1065 AND PDE LLa
  162350. GABRIEL WEATHERHEAD
  162351. 9734N
  162352. 2/28/96V`A REVIEW. S. RAJESWARI ET AL., HETEROCYCLES, 25, 659 (1987). SYNTHESES OF INDOLIZIDINE ALKALOIDSa
  162353. GABRIEL WEATHERHEAD
  162354. 9735N
  162355. 2/28/96V
  162356. A REVIEW. J.P. KUTNEY, HETEROCYCLES, 25, 617 (1987). STUDIES IN PLANT TISSUE CULTURE. THE SYNTHESIS AND BIOSYNTHESIS OF INDOLE ALKALOIDSa
  162357. GABRIEL WEATHERHEAD
  162358. 9736N
  162359. 2/28/96V
  162360. A REVIEW. S.J. DANISHEFSKY, ALDRICHIMICA ACTA, 19, 59 (1986). REFLECTIONS ON ORGANIC SYNTHESIS: THE EVOLUTION OF A GENERAL STRATEGY FOR THE STEREOSELECTIVE CONSTRUCTION OF POLYOXYGENATED NATURAL PRODUCTSa
  162361. GABRIEL WEATHERHEAD
  162362. 9737N
  162363. 2/28/96V[A REVIEW. J.J. MCCULLOUGH, CHEM. REV., 87, 811 (1987). PHOTOADDITIONS OF AROMATIC COMPOUNDSa
  162364. GABRIEL WEATHERHEAD
  162365. 9738N
  162366. 2/28/96
  162367. VqA REVIEW. V. RAMAMURTHY AND K. VENKATESAN, CHEM. REV., 87, 433 (1987). PHOTOCHEMICAL REACTIONS OF ORGANIC CYSTALSa
  162368. GABRIEL WEATHERHEAD
  162369. 9739N
  162370. 2/28/96VfA REVIEW. B. ALCERMARK, CHEM. SCR., 27 (1987). SYMPOSIUM: SYNTHETIC SELECTIVITY: A TIME OF OPPORTUNITYa
  162371. GABRIEL WEATHERHEAD
  162372. 9740N
  162373. 2/28/96VcA REVIEW. T. SUAMI, PURE APPL. CHEM., 59, 1509 (1987). SYNTHETIC VENTURES IN PSEUDO SUGAR CHEMISTRYa
  162374. GABRIEL WEATHERHEAD
  162375. 9741N
  162376. 2/28/96VVA REVIEW. G. ADAM AND V. MARQUARDT, Z. CHEM., 41 (1987). SYNTHESIS OF BRASSINOSTEROIDSa
  162377. GABRIEL WEATHERHEAD
  162378. 9742N
  162379. 2/28/96V
  162380. A REVIEW. Z.V. TODRES, TETRAHEDRON, 43, 3839 (1987). TETRAHEDRON REPORT 224: ETHYLENIC COMPOUNDS AS PROBES FOR THE STUDY OF DONOR ACCEPTOR INTERACTIONa
  162381. GABRIEL WEATHERHEAD
  162382. 9743N
  162383. 2/28/96VYA REVIEW. T.W. BASTOCK, SPEC. CHEM., 7, 382 (1987). NEW SYNTHETIC ROUTES TO OLD MOLECULESa
  162384. GABRIEL WEATHERHEAD
  162385. 9744N
  162386. 2/28/96VJA REVIEW. G.A. OLAH ET AL., CHEM. REV., 87, 671 (1987). FORMYLATING AGENTSa
  162387. GABRIEL WEATHERHEAD
  162388. 9745N
  162389. 2/28/96ViA REVIEW. G.P. ELLIS AND T.M. ROMNEY ALEXANDER, CHEM. REV., 87, 779 (1987). CYANATION OF AROMATIC HALIDESa
  162390. GABRIEL WEATHERHEAD
  162391. 9746N
  162392. 2/28/96V
  162393. A REVIEW. A.S. KERTES AND C.J. KING, CHEM. REV., 87, 687 (1987). EXTRACTION CHEMISTRY OF LOW MOLECULAR WEIGHT ALIPHATIC ALCOHOLSa
  162394. GABRIEL WEATHERHEAD
  162395. 9747N
  162396. 2/28/96V
  162397. A REVIEW. C O. BUCHECKER AND J. P. SAUVAGE, CHEM. REV., 87, INTERLOCKING OF MOLECULAR THREADS: FROM THE STATISTICAL APPROACH TO THE TEMPLATED SYNTHESIS OF CATENANDSa
  162398. GABRIEL WEATHERHEAD
  162399. 9748N
  162400. 2/28/96VpA REVIEW. M. TANAKA, J. SYNTH. ORG. CHEM., JPN., 45, 716 (1987). A PERSPECTIVE VIEW OF CARBON MONOXIDE CHEMISTRYa
  162401. GABRIEL WEATHERHEAD
  162402. 9749N
  162403. 2/28/96
  162404. VfA REVIEW. G.R. KROW, TETRAHEDRON, 43, 1 (1987). ONE CARBON RING EXPANSIONS OF BRIDGED BICYCLIC KETONESa
  162405. GABRIEL WEATHERHEAD
  162406. 9750N
  162407. 2/28/96VtA REVIEW. B. HALTON AND P.J. STANG, ACC. CHEM. RES., 20, 443 (1987). ALKYLIDENECYCLOPROPARENES AND RELATED COMPOUNDSa
  162408. GABRIEL WEATHERHEAD
  162409. 9751N
  162410. 2/28/96VpA REVIEW. A. COLLET, TETRAHEDRON, 43, 5725 (1987). TETRAHEDRON REPORT 226: CYCLOTRIVERATRYLENES AND CRYPTOPHANESa
  162411. GABRIEL WEATHERHEAD
  162412. 9752N
  162413. 2/28/96VmA REVIEW. R. WEST, ANGEW. CHEM. INT. ED. ENGL., 26, 1201 (1987). CHEMISTRY OF THE SILICON SILICON DOUBLE BONDa
  162414. GABRIEL WEATHERHEAD
  162415. 9753N
  162416. 2/28/96VVA REVIEW. G.A. OLAH, ACC. CHEM. RES., 20, 422 (1987). ELECTROPHILIC METHANE CONVERSIONa
  162417. GABRIEL WEATHERHEAD
  162418. 9754N
  162419. 2/28/96V~A REVIEW. H. HASHIMOTO AND N.KAWAGUCHI, J. SYNTH. ORG. CHEM., JPN., 45, 408 (1987). NEW CHIRAL SYNTHONS DERIVED FROM D GLUCOSEa
  162420. GABRIEL WEATHERHEAD
  162421. 9755N
  162422. 2/28/96V
  162423. A REVIEW. H. KOSUGI, J. SYNTH. ORG. CHEM., JPN., 45, 472 (1987). ASYMMETRIC SYNTHESIS OF NATURAL PRODUCTS USING CHIRAL SULPHOXIDESa
  162424. GABRIEL WEATHERHEAD
  162425. 9756N
  162426. 2/28/96VsA REVIEW. R.M. WILLIAMS, PERGAMON PRESS, ORGANIC CHEMISTRY VOL.8. BOOK: SYNTHESIS OF OPTICALLY ACTIVE A AMINO ACIDSa
  162427. GABRIEL WEATHERHEAD
  162428. 9757N
  162429. 2/28/96VyA REVIEW. T. NAGAHARA AND T. KAMETANI, HETEROCYCLES, 25, 729 (1987). ENANTIOSELECTIVE SYNTHESES OF CARBAPENAM ANTIBIOTICSa
  162430. GABRIEL WEATHERHEAD
  162431. 9758N
  162432. 2/28/96V
  162433. A REVIEW. H.E. ZIMMERMAN, ACC. CHEM. RES., 20, 263 (1987). KINETIC PROTONATION OF ENOLS, ENOLATES AND ANALOGS. THE STEREOCHEMISTRY OF KETONIZATIONa
  162434. GABRIEL WEATHERHEAD
  162435. 9759N
  162436. 2/28/96VrA REVIEW. Y. YAMAMOTO, ACC. CHEM. RES., 2O, 243 (1987). ACYCLIC STEREOCONTROL VIA ALLYLIC ORGANOMETALLIC COMPOUNDSa
  162437. GABRIEL WEATHERHEAD
  162438. 9760N
  162439. 2/28/96
  162440. A REVIEW. S. SUZUKI AND Y. ONO, J. SYNTH. ORG. CHEM. JPN., 45, 672 (1987). NOVEL SOLID ACID CATALYST    POLYORGANO SILOXANE BEARING S03H GROUPSa
  162441. GABRIEL WEATHERHEAD
  162442. 9761N
  162443. 2/28/96VeA REVIEW. N.S. ISAACS AND A.V. GOERGE, CHEM. BR , 23, 47 (1987). CHEMICAL SYNTHESIS AT HIGH PRESSURESa
  162444. GABRIEL WEATHERHEAD
  162445. 9762N
  162446. 2/28/96VoA REVIEW. D.D. PERRIN AND W.L.F. ARMAREGO, PERGAMON PRESS. BOOK: PURIFICATION OF LABORATORY CHEMICALS (3RD ED.)a
  162447. GABRIEL WEATHERHEAD
  162448. 9763N
  162449. 2/28/96V
  162450. A REVIEW. T.J. SIMPSON, CHEM. SOC. REV., 16, 123 (1987). APPLICATIONS OF MULTINUCLEAR NMR TO STRUCTURAL AND BIOSYNTHETIC STUDIES OF POLYKETIDE MICROBIAL METABOLITESa
  162451. GABRIEL WEATHERHEAD
  162452. 9764N
  162453. 2/28/96
  162454. iA REVIEW. J. LINDLEY AND T.J. MASON, CHEM.SOC. REV., 16, 275 SONOCHEMISTRY. PART 2   SYNTHETIC APPLICATIONS  R. P. SHERIDAN AND R. VENKATARAGHAVAN, ACC. CHEM. RES., 20, 322 (1987). NEW METHODS IN COMPUTER AIDED DRUG DESIGN  A.J. KRESGE, ACC. CHEM. RES., 20, 364 (1987). UNUSUAL REACTIVITY OF PROSTACYCLIN: RATIONAL DRUG DESIGN THROUGH PHYSICAL ORGANIC CHEMISTRY
  162455. GABRIEL WEATHERHEAD
  162456. 9765N
  162457. 2/28/96VJA REVIEW. M.A. PARISH, SPEC. CHEM., 7, 366 (1987). CYCLODEXTRINS, A REVIEWa
  162458. GABRIEL WEATHERHEAD
  162459. 9766N
  162460. 2/28/96VzA REVIEW. B.R. VENEPALLI AND W.C. AGOSTA, CHEM. REV., 87, 399 (1987). FENESTRANES AND THE FLATTENING OF TETRAHEDRAL CARBONa
  162461. GABRIEL WEATHERHEAD
  162462. 9767N
  162463. 2/28/96VdA REVIEW. M. TISLER, ORG. PREP. PROCED. INT., 18, 17 (1986). SYNTHETIC APPROACHES TO BISNAPHTHALENESa
  162464. GABRIEL WEATHERHEAD
  162465. 9768N
  162466. 2/28/96
  162467. VqA REVIEW. J.L. CHARLTON AND M.M. ALAUDDIN, TETRAHEDRON, 43, 2873 (1987). TETRAHEDRON REPORT: ORTHOQUINODIMETHANESa
  162468. GABRIEL WEATHERHEAD
  162469. 9769N
  162470. 2/28/96VXA REVIEW. H. VIOLA, Z.CHEM., 27, 15 (1987). REAGENTS FOR THIOLATION IN ORGANIC CHEMISTRYa
  162471. GABRIEL WEATHERHEAD
  162472. 9770N
  162473. 2/28/96V_A REVIEW. D.J.R. MASSY, SYNTHESIS, 589 (1987). REVIEW A THIOALKYLATION VIA ALDEHYDES AND THIOLSa
  162474. GABRIEL WEATHERHEAD
  162475. 9771N
  162476. 2/28/96V[A REVIEW. E. BREITMAIER ET AL., SYNTHESIS, 1 (1987). 3 ALKOXYACROLEINS IN ORGANIC SYNTHESISa
  162477. GABRIEL WEATHERHEAD
  162478. 9772N
  162479. 2/28/96V
  162480. A REVIEW. B.P. CHO AND R.G. HARVEY, J. ORG. CHEM., 52, 5668 (1987). POLYCYCLIC FLUORANTHENE HYDROCARBONS. 2. A NEW GENERAL SYNTHESISa
  162481. GABRIEL WEATHERHEAD
  162482. 9773N
  162483. 2/28/96VuA REVIEW. J.E. JACKSON ET AL., TETRAHEDRON, 43, 653 (1987). REACTION OF DIFLUOROCARBENE WITH SMALL BICYCLIC MOLECULESa
  162484. GABRIEL WEATHERHEAD
  162485. 9774N
  162486. 2/28/96V
  162487. A REVIEW. J.T. WELCH, TETRAHEDRON, 43, 3123 (1987). TETRAHEDRON REPORT 221: ADVANCES IN THE PREPARATION OF BIOLOGICALLY ACTIVE ORGANOFLUORINE COMPOUNDSa
  162488. GABRIEL WEATHERHEAD
  162489. 9775N
  162490. 2/28/96V
  162491. A REVIEW. T. KITAZUME AND T. YAMAZAKI, J. SYNTH. ORG. CHEM.,JPN., 45, 888 (1987). NEW CATALYTIC REACTIONS OF HYDROLYTIC ENZYMES IN FLUORINE CHEMISTRYa
  162492. GABRIEL WEATHERHEAD
  162493. 9776N
  162494. 2/28/96VpA REVIEW. D.W. RIBBONS ET AL., J. FLUORINE CHEM., 37, 299 (1987). BIOTRANSFORMATIONS OF FLUOROAROMATIC COMPOUNDSa
  162495. GABRIEL WEATHERHEAD
  162496. 9777N
  162497. 2/28/96VxA REVIEW. L.M. YAGUPOLSKII, J. FLUOR. CHEM., 36, 1 (1987). AROMATIC COMPOUNDS WITH NEW FLUORINE  CONTAINING SUBSTITUENTSa
  162498. GABRIEL WEATHERHEAD
  162499. 9778N
  162500. 2/28/96V
  162501. A REVIEW. J. F. NORMANT AND C. WAKSELMAN, BULL. SOC. CHEM. FR., 6, 858 (1986). NEW TRENDS IN FLUORINATED ORGANIC COMPOUNDS CHEMISTRYa
  162502. GABRIEL WEATHERHEAD
  162503. 9779N
  162504. 2/28/96
  162505. A REVIEW. J. FLUORINE CHEM., 35, 1 (1987). SYNPOSIUM: PROCEEDINGS OF THE INTERNATIONAL SYMPOSIUM TO MARK THE CENTENARY OF THE ISOLATION OF FLUORINEa
  162506. GABRIEL WEATHERHEAD
  162507. 9780N
  162508. 2/28/96V
  162509. A REVIEW. A. MAERCKER, ANGEW. CHEM., INT. ED. ENGL., 26, 972 (1987). ETHER CLEAVAGE WITH ORGANO ALKALI METAL COMPOUNDS AND ALKALI METALSa
  162510. GABRIEL WEATHERHEAD
  162511. 9781N
  162512. 2/28/96V
  162513. A REVIEW. A. MAERCKER AND M. THEIS, TOP. CURR. CHEM., 138, 1 (1987). SOME ASPECTS OF THE CHEMSITRY OF POLYLITHIATED ALIPHATIC HYDROCARBONSa
  162514. GABRIEL WEATHERHEAD
  162515. 9782N
  162516. 2/28/96VjA REVIEW. D.H.R. BARTON ET AL., PURE APPL. CHEM., 59, 937 (1987). BISMUTH(V) REAGENTS IN ORGANIC SYNTHESISa
  162517. GABRIEL WEATHERHEAD
  162518. 9783N
  162519. 2/28/96VuA REVIEW. H. SUZUKI, J. SYNTH. ORG. CHEM., JPN., 45, 603 (1987). ORGANIC TRANSFORMATIONS BASED ON TELLURIUM COMPOUNDSa
  162520. GABRIEL WEATHERHEAD
  162521. 9784N
  162522. 2/28/96
  162523. VoA REVIEW. G.L. LARSON, J. ORGANOMET. CHEM., 337, 195 (1987). ORGANOSILICON SURVEY 1985. THE SILICON CARBON BONDa
  162524. GABRIEL WEATHERHEAD
  162525. 9785N
  162526. 2/28/96V{A REVIEW. J.T. MAGUE, J. ORGANOMET.CHEM., 324, 57 (1987). COBALT, RHODIUM AND IRIDIUM: ANNUAL SURVEY COVERING THE YEAR 1985a
  162527. GABRIEL WEATHERHEAD
  162528. 9786N
  162529. 2/28/96VtA REVIEW. G.O. DOAK AND L.D. FREEDMAN, J. ORGANOMET.CHEM., 324, 39 (1987). BISMUTH: ANNUAL SURVEY COVERING YEAR 1985a
  162530. GABRIEL WEATHERHEAD
  162531. 9787N
  162532. 2/28/96VuA REVIEW. L.D. FREEDMAN AND G. DOAK, J. ORGANOMET. CHEM., 324, (1987). ANTIMONY: ANNUAL SURVEY COVERING THE YEAR 1985a
  162533. GABRIEL WEATHERHEAD
  162534. 9788N
  162535. 2/28/96VzA REVIEW. H.B. KAGAN AND J.L. NAMY, TETRAHEDRON, 42, 6573 (1987). TETRAHEDRON REPORT 213: LANTHANIDES IN ORGANIC SYNTHESISa
  162536. GABRIEL WEATHERHEAD
  162537. 9789N
  162538. 2/28/96
  162539. VhA REVIEW. W.H. ILSLEY, J. ORGANOMET. CHEM., 337, 1 (1987). MERCURY: ANNUAL SURVEY COVERING THE YEAR 1980a
  162540. GABRIEL WEATHERHEAD
  162541. 9790N
  162542. 2/28/96VuA REVIEW. P.A. SHAPLEY, J. ORGANOMET. CHEM., 318, 409 (1987). ANNUAL SURVEY OF RUTHENIUM AND OSMIUM FOR THE YEAR 1984a
  162543. GABRIEL WEATHERHEAD
  162544. 9791N
  162545. 2/28/96VsA REVIEW. J.B. KEISTER, J. ORGANOMET. CHEM., 318, 297 (1987). RUTHENIUM AND OSMIUM: ANNUAL SURVEY FOR THE YEAR 1983a
  162546. GABRIEL WEATHERHEAD
  162547. 9792N
  162548. 2/28/96V
  162549. A REVIEW. T. MITSUDO, Y. HORI AND Y. WATANABE, J. ORGANOMET. CHEM., 334, 157 (1987). NOVEL ORGANIC SYNTHESES CATALYZED BY (CYCLOOCTADIENE)(CYCLOOCTATRIENE) RUTHENIUM AND ITS DERIVATIVESa
  162550. GABRIEL WEATHERHEAD
  162551. 9793N
  162552. 2/28/96VwA REVIEW. R.C. KERBER, J. ORQANOMET. CHEM., 318, 157 (1987). ORGANOIRON CHEMISTRY: ANNUAL SURVEY COVERING THE YEAR 1985a
  162553. GABRIEL WEATHERHEAD
  162554. 9794N
  162555. 2/28/96
  162556. V|A REVIEW. B.M. ROCKETT AND G. MARR, J. ORGANOMET. CHEM., 318, 231 ( 1987 ) . FERROCENE: ANNUAL SURVEY COVERING THE YEAR 1985a
  162557. GABRIEL WEATHERHEAD
  162558. 9795N
  162559. 2/28/96VnA REVIEW. M. HIROBE, J. SYNTH. ORG. CHEM., JPN., 45, 755 (1987). CATALYTIC REACTIONS BY IRON SULPHUR COMPLEXESa
  162560. GABRIEL WEATHERHEAD
  162561. 9796N
  162562. 2/28/96V
  162563. A REVIEW. M.H. CHISHOLM, NEW. J. CHEM., 11, 459 (1987). CLEAVAGE AND FORMATION OF CARBON CARBON AND CARBON OXYGEN BONDS IN REACTIONS INVOLVING DIMOLYBDENUM AND DITUNGSTEN HEXAALKOXIDESa
  162564. GABRIEL WEATHERHEAD
  162565. 9797N
  162566. 2/28/96V
  162567. A REVIEW. S. KATO, T. MURAI AND M. ISHIDA, ORG. PREP. PROCED. INT., 18, 369 (1986). SELENIUM AND TELLURIUM ISOLOGUES OF CARBOXYLIC ACID DERIVATIVESa
  162568. GABRIEL WEATHERHEAD
  162569. 9798N
  162570. 2/28/96
  162571. A REVIEW. J. TSUJI AND I. MINAMI, ACC. CHEM. RES., 20, 140 (1987). NEW SYNTHETIC REACTIONS OF ALLYL, ALKYL CARBONATES, ALLYL B KETO CARBOXYLATES AND ALLYL VINYLIC CARBONATES CATALYZED BY PALLADIUM COMPLEXESa
  162572. GABRIEL WEATHERHEAD
  162573. 9799N
  162574. 2/28/96V
  162575. A REVIEW. P.A. CHALONER, J. ORGANOMET. CHEM., 337, 431 (1987). NICKEL, PALLADIUM AND PLATINUM: ANNUAL SURVEY COVERING THE YEAR 1981a
  162576. GABRIEL WEATHERHEAD
  162577. 9800N
  162578. 2/28/96V
  162579. A REVIEW. P.A. CHALONER, J. ORGANOMET. CHEM., 324, 283 (1987). NICKEL, PALLADIUM AND PLATINUM: ANNUAL SURVEY COVERING THE YEAR 1980a
  162580. GABRIEL WEATHERHEAD
  162581. 9801N
  162582. 2/28/96V
  162583. A REVIEW. K. UTIMOTO, J. SYNTH. ORG. CHEM. JPN., 45, 112 (1987). ORGANIC SYNTHESIS WITH PALLADIUM CATALYSTS. INTRAMOLECULAR ADDITION OF OH, NH, AND C02H TO AN ACETYLENE MOIETYa
  162584. GABRIEL WEATHERHEAD
  162585. 9802N
  162586. 2/28/96
  162587. VxA REVIEW. H.C. COLQUHOUN, CHEM. IND.(LONDON), 612 (1987). HOMOGENEOUS, PALLADIUM CATALYZED, CARBON CARBON BOND FORMATIONa
  162588. GABRIEL WEATHERHEAD
  162589. 9803N
  162590. 2/28/96VcA REVIEW. Y. YAMAMOTO, ALDRICHIMICA ACTA, 20, 45 (1987). ALLYLIC TIN COMPOUNDS IN ORGANIC SYNTHESISa
  162591. GABRIEL WEATHERHEAD
  162592. 9804N
  162593. 2/28/96V
  162594. A REVIEW. P.A. SUTTON AND D.A. BUCKINGHAM, ACC. CHEM. RES., 20, 357 (1987). COBALT(III) PROMOTED HYDROLYSIS OF AMINO ACID ESTERS AND PEPTIDES AND THE SYNTHESIS OF SMALL PEPTIDESa
  162595. GABRIEL WEATHERHEAD
  162596. 9805N
  162597. 2/28/96V{A REVIEW. E. ERDIK, TETRAHEDRON, 43, 2203 (1987). TETRAHEDRON REPORT 217: USE OF ACTIVATION METHODS FOR ORGANOZINC REAGENTSa
  162598. GABRIEL WEATHERHEAD
  162599. 9806N
  162600. 2/28/96V
  162601. A REVIEW. E. NEGISHI, ACC. CHEM. RES., 20, 65 (1987). CONTROLLED CARBOMETALLATION AS A NEW TOOL FOR CARBON CARBON BOND FORMATION AND ITS APPLICATION TO CYCLIZATIONa
  162602. GABRIEL WEATHERHEAD
  162603. 9807N
  162604. 2/28/96
  162605. A REVIEW. H. KAGAN, BULL. SOC. CHIM. FR., 4, 607 (1987). CHEMISTRY OF ORGANOMETALLICS AND THEIR APPLICATIONS IN ORGANIC SYNTHESISa
  162606. GABRIEL WEATHERHEAD
  162607. 9808N
  162608. 2/28/96VqA REVIEW. M. VEITH, ANGEW. CHEM. INT. ED. ENGL., 26, 1 (1987). UNSATURATED MOLECULES CONTAINING MAIN GROUP METALSa
  162609. GABRIEL WEATHERHEAD
  162610. 9809N
  162611. 2/28/96VvA REVIEW. B.H. LIPSHUTZ, SYNTHESIS, 3Z5 (1987). APPLICATIONS OF HIGHER ORDER MIXED ORGANOCUPRATES TO ORGANIC SYNTHESISa
  162612. GABRIEL WEATHERHEAD
  162613. 9810N
  162614. 2/28/96VqA REVIEW. A.J. FATIADI, SYNTHESIS, 959 (1987). NEW APPLICATIONS OF TETRACYANOETHYLENE IN ORGANOMETALLIC CHEMISTRYa
  162615. GABRIEL WEATHERHEAD
  162616. 9811N
  162617. 2/28/96V
  162618. A REVIEW. J. DUBAC AND A. LAPORTERIE, CHEM. REV., 87, 319 (1987). ENE AND RETRO ENE REACTIONS OF GROUP 14 ORGANOMETALLIC CHEMISTRYa
  162619. GABRIEL WEATHERHEAD
  162620. 9812N
  162621. 2/28/96
  162622. A REVIEW. J.M. O'CONNOR AND C.P. CASEY, CHEM. REV., 87, 307(1987). RING SLIPPAGE CHEMISTRY OF TRANSITION METAL CYCLOPENTADIENYL AND INDENYL COMPLEXESa
  162623. GABRIEL WEATHERHEAD
  162624. 9813N
  162625. 2/28/96V|A REVIEW. J. I. SETSUNE AND D. DOLPHIN, CAN. J. CHEM., 65, 459 (1987). ORGANOMETALLIC ASPECTS OF CYTOCHROME P 450 METABOLISMa
  162626. GABRIEL WEATHERHEAD
  162627. 9814N
  162628. 2/28/96V
  162629. A REVIEW. J. DUNOGUES, BULL. SOC. CHIM. FR., 659 (1987). COLLOQUIUM SEMINAR: ORGANOSILICONS, SELECTIVE INTERMEDIATES FOR THE SYNTHESIS OF FINE ORGANICSa
  162630. GABRIEL WEATHERHEAD
  162631. 9815N
  162632. 2/28/96V
  162633. A REVIEW. T.A. O'DONNELL, CHEM. SOC. REV., 16, 1 (1987). STABILIZATION OF UNUSUAL CATIONIC SPECIES IN PROTONIC SUPERACIDS AND ACIDIC MELTSa
  162634. GABRIEL WEATHERHEAD
  162635. 9816N
  162636. 2/28/96VnA REVIEW. F. TURECEK, COLL CZECH. CHEM. COMMUN., 1928 (1987). STEREOCHEMISTRY OF ORGANIC IONS IN THE GAS PHASEa
  162637. GABRIEL WEATHERHEAD
  162638. 9817N
  162639. 2/28/96
  162640. V~A REVIEW. K.M. NICHOLAS, ACC. CHEM. RES., 20, 207 (1987). CHEMISTRY AND SYNTHETIC UTILITY OF COBALTCOMPLEXED PROPARGYL CATIONSa
  162641. GABRIEL WEATHERHEAD
  162642. 9818N
  162643. 2/28/96V
  162644. A REVIEW. J.A. CHUDEK AND R. FOSTER, GAZZ. CHIM. ITAL., 117, 629 (1987). FORMATION AND REACTIONS OF SIGMA ANIONIC COMPOUNDS (JACKSON MEISENHEIMER ADDUCTS) IN LIQUID AMMONIA STUDIES BY LH AND 13C NMRa
  162645. GABRIEL WEATHERHEAD
  162646. 9819N
  162647. 2/28/96VvA REVIEW. H. BOCK AND R. DAMMEL, ANGEW. CHEM. INT. ED. ENGL., 26, 504 (1987). THE PYROLYSIS OF AZIDES IN THE GAS PHASEa
  162648. GABRIEL WEATHERHEAD
  162649. 9820N
  162650. 2/28/96ViA REVIEW. 0. METH COHN, ACC. CHEM. RES., 20, 18 (1987). NEW SYNTHETIC APPLICATIONS OF OXYCARBONYLNITRENESa
  162651. GABRIEL WEATHERHEAD
  162652. 9821N
  162653. 2/28/96V
  162654. A REVIEW. YU.G. GOLOLOBOV ET AL., TETRAHEDRON, 43, 2609 (1987). TWENTY FIVE YEARS OF DIMETHYLSULFOXONIUM METHYLIDE (COREY'S REAGENT)a
  162655. GABRIEL WEATHERHEAD
  162656. 9822N
  162657. 2/28/96
  162658. A REVIEW. F. MATHEY, ANGEW. CHEM. INT. ED. ENGL., 26, 275 (1987), THE DEVELOPMENT OF A CARBENE LIKE CHEMISTRY WITH TERMINAL PHOSPHINIDENE COMPLEXESa
  162659. GABRIEL WEATHERHEAD
  162660. 9823N
  162661. 2/28/96V
  162662. A REVIEW. O.A. ATTANASI AND L. CAGLIOTI, ORG. PREP. PROCED. INT., 18, 299 (1986). CONJUGATED AZOALKENES: ATTRACTIVE PRODUCTS AND VERSATILE INTERMEDIATESa
  162663. GABRIEL WEATHERHEAD
  162664. 9824N
  162665. 2/28/96V
  162666. A REVIEW. K.M. SMITH AND J.A.S. CAVALEIRO, HETEROCYCLES, 26, 1947 (1987). PROTOPORPHYRIN IX: SOME USEFUL SUBSTITUENT MANIPULATIONSa
  162667. GABRIEL WEATHERHEAD
  162668. 9825N
  162669. 2/28/96VtA REVIEW. Y. MATSUDA AND H. GOTON, HETEROCYCLES, 26, 2757 (1987). THE CHEMISTRY OF ANTIAROMATIC AZACYCL[3.3.3]AZINESa
  162670. GABRIEL WEATHERHEAD
  162671. 9826N
  162672. 2/28/96V_A REVIEW. S. GRASSO, M. ZAPPALA AND A. CHIMIRRI, HETEROCYCLES, 26, 2477 (1987). BENZODIAZOCINESa
  162673. GABRIEL WEATHERHEAD
  162674. 9827N
  162675. 2/28/96
  162676. A REVIEW. G. MOHIUDDIN, P.S. REDDY, K. AHMED AND C.V. RATNAM, HETEROCYCLES, 24, 3489 (1986). RECENT ADVANCES IN THE SYNTHESIS OF ANNULATED 1,4 BENZODIAZEPINESa
  162677. GABRIEL WEATHERHEAD
  162678. 9828N
  162679. 2/28/96V
  162680. A REVIEW. Y. OKAMOTO AND K. TAKAGI, J. HETEROCYCL. CHEM. 24, 885 (1987) CHEMISTRY OF 4 AMINO 1H 1,5 BENZODIAZEPINE 3 CARBONITRILEa
  162681. GABRIEL WEATHERHEAD
  162682. 9829N
  162683. 2/28/96V
  162684. A REVIEW. I.I. GRANDBERG, L.K. DENISOV AND O.A. POPOVA, CHEM. HETEROCYCL. COMPD. (ENGL. TRANS.), 23, 117 (1987). 7 AMINOCOUMARINSa
  162685. GABRIEL WEATHERHEAD
  162686. 9830N
  162687. 2/28/96VmA REVIEW. A. LEVAL, CHEM. HETEROCYCL. COMPDS., (ENGL. TRANS.), 22, 1161 (1986). SYNTHESIS OF BENZOTHIAZEPINESa
  162688. GABRIEL WEATHERHEAD
  162689. 9831N
  162690. 2/28/96V
  162691. A REVIEW. C.K. GHOSH, C. BANDYOPADHYAY AND J. MAITI, HETEROCYCLES, 26, 1623 (1987). HETEROCYCLES FUSED WITH THE 2,3 BOND OF [1]BENZOPYRANa
  162692. GABRIEL WEATHERHEAD
  162693. 9832N
  162694. 2/28/96
  162695. VzA REVIEW. T.M. ROMNEY ALEXANDER, HETEROCYCLES, 26, 1899 (1987). BENZOPYRAN 4 ONES CONTAINING A 2,3 FUSED HETEROCYCLIC RINGa
  162696. GABRIEL WEATHERHEAD
  162697. 9833N
  162698. 2/28/96V
  162699. A REVIEW. S. SARAF, F. AL OMRAN AND B. AL SALEH, HETEROCYCLES, 26, 239 (1987). RECENT ADVANCES IN THE SYNTHESIS OF PHENOTHIAZINESa
  162700. GABRIEL WEATHERHEAD
  162701. 9834N
  162702. 2/28/96V
  162703. A REVIEW. M.J. HEARN AND F. LEVY. ORG. PREP. PROCED. INTL. 19, 215 (1987) RECENT PROGRESS IN THE SYNTHESIS AND REACTIONS OF TETRAZINESa
  162704. GABRIEL WEATHERHEAD
  162705. 9835N
  162706. 2/28/96V
  162707. A REVIEW. K. SENGA, J. SYNTH. ORG. CHEM. JPN., 45, 318 (1987). SYNTHESIS OF FUSED PYRIMIDINES FROM HYDRAZINOPYRIMIDINES AND THEIR RELATED COMPOUNDSa
  162708. GABRIEL WEATHERHEAD
  162709. 9836N
  162710. 2/28/96V
  162711. A REVIEW. A. KATOH, T. NISHIO AND C. KASHIMA, HETEROCYCLES, 26, 2223 (1987). SYNTHESIS AND REACTIONS OF N SUBSTITUTED 2(1H) PYRIMIDONES AND PYRIMIDINETHIONESa
  162712. GABRIEL WEATHERHEAD
  162713. 9837N
  162714. 2/28/96
  162715. A REVIEW. G. HEINISCH, HETEROCYCLES, 26, 481 (1987). ADVANCES IN THE SYNTHESIS OF SUBSTITUTED PYRIDAZINES VIA INTRODUCTION OF CARBON FUNCTIONAL GROUPS INTO THE PARENT HETEROCYCLEa
  162716. GABRIEL WEATHERHEAD
  162717. 9838N
  162718. 2/28/96V\A REVIEW. G. HALL, J.K. SUGDEN AND M.B. WAGHELA, SYNTHESIS, 10 (1987). PYRRAZOLINE CHEMISTRYa
  162719. GABRIEL WEATHERHEAD
  162720. 9839N
  162721. 2/28/96V
  162722. A REVIEW. N. FURAKAWA, J. SYNTH. ORG. CHEM. JPN., 45, 624 (1987). REACTIONS OF PYRIDYL AND RELATED HETEROAROMATICS ACTIVATED BY SULPHUR FUNCTIONAL GROUPSa
  162723. GABRIEL WEATHERHEAD
  162724. 9840N
  162725. 2/28/96V
  162726. A REVIEW.  V.A. BAKULEV AND V.S. MOKRUSHIN, CHEM. HETEROCYCL. COMPDS., (ENGL. TRANSL.), 22, 811 (1986). STRUCTURES, SYNTHESIS AND PROPERTIES OF 1,2,3 THIADIAZOLESa
  162727. GABRIEL WEATHERHEAD
  162728. 9841N
  162729. 2/28/96VTA REVIEW. B.L. FERINGA, REC. TRAV. CHIM., 106, 469 (1987). PHOTO OXIDATION OF FURANSa
  162730. GABRIEL WEATHERHEAD
  162731. 9842N
  162732. 2/28/96
  162733. A REVIEW. S. GRONOWITZ, J. WILEY (1987). BOOK: THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS. VOLUME 55, PART 3: THIOPHENE AND ITS DERIVATIVESa
  162734. GABRIEL WEATHERHEAD
  162735. 9843N
  162736. 2/28/96V[A REVIEW. A.K. MUKERJEE, HETEROCYCLES, 26, 1077 (1987). AZLACTONES: RETROSPECT AND PROSPECTa
  162737. GABRIEL WEATHERHEAD
  162738. 9844N
  162739. 2/28/96VxA REVIEW.  H. HEIMGARTNER, ISR. J. CHEM., 27, 3 (1986). THE APPLICATION OF 3 AMINO 2H AZIRINES AS AMINO ACID EQUIVALENTSa
  162740. GABRIEL WEATHERHEAD
  162741. 9845N
  162742. 2/28/96V
  162743. A REVIEW. C. KASHIMA AND T. TAJIMA, J. SYNTH. ORG. CHEM., JPN., 45, 863 (1987). THE SYNTHESIS AND REACTIONS OF B IMIDAZOLYL ENONESa
  162744. GABRIEL WEATHERHEAD
  162745. 9846N
  162746. 2/28/96V
  162747. A REVIEW.  L.I. BELEN'KII, CHEM. HETEROCYCL. COMPD., 22 (1986). EFFECT OF THE ACID BASE PROPERTIES OF HETEROAROMATIC COMPOUNDS ON THEIR ELECTROPHILIC SUBSTITUTION REACTIONSa
  162748. GABRIEL WEATHERHEAD
  162749. 9847N
  162750. 2/28/96
  162751. A REVIEW. H.C. VAN DER PLAS, M. SIMONYI, F.C. ALDERWEIRELDT AND J.A. LEPOIURE, ELSEVIER SCIENCE PUBLISHERS, 1986. BOOK: BIO ORGANIC HETEROCYCLES, 1986: SYNTHESIS, MECHANISMS AND BIOACTIVITYa
  162752. GABRIEL WEATHERHEAD
  162753. 9848N
  162754. 2/28/96VPA REVIEW. E. BREUER, ISR. J. CHEM., 27 (1986). HETEROCYCLES IN ORGANIC SYNTHESISa
  162755. GABRIEL WEATHERHEAD
  162756. 9849N
  162757. 2/28/96V~A REVIEW.  A.R. KATRITZKY, C.M. MARSON AND H. FAID ALLAH, HETEROCYCLES, 26, 1657 (1987). HETEROCYCLIC N THIODICARBOXYLIC ACIDSa
  162758. GABRIEL WEATHERHEAD
  162759. 9850N
  162760. 2/28/96V
  162761. A REVIEW.  A.R. KATRITZKY, H. FAID ALLAH AND C.M. MARSON, HETEROCYCLES, 26, 1333 (1987). THE N CARBOXYLIC ACIDS OF NITROGEN HETEROCYCLESa
  162762. GABRIEL WEATHERHEAD
  162763. 9851N
  162764. 2/28/96VtA REVIEW. V.A. DOMBROVSKII ET AL., RUSS. CHEM. REV., 55, 978 (1986). THE SYNTHESIS OF PROSTACYCLIN AND ITS ANALOGUESa
  162765. GABRIEL WEATHERHEAD
  162766. 9852N
  162767. 2/28/96
  162768. VhA REVIEW. E.D. MATVEEVA ET AL., RUSS. CHEM. REV., 55, 672(1987). THE SYNTHESIS OF LEPIDOPTERA PHEROMONESa
  162769. GABRIEL WEATHERHEAD
  162770. 9853N
  162771. 2/28/96V
  162772. A REVIEW. AE. DE GROOT AND T.A. VAN BEEK, RECL. TRAV. CHIM., 106, 1 (1987). TERPENOID ANTIFEEDANTS (PART II). THE SYNTHESIS OF DRIMANE AND CLERODANE INSECT ANTIFEEDANTSa
  162773. GABRIEL WEATHERHEAD
  162774. 9854N
  162775. 2/28/96V
  162776. A REVIEW. H.H. WASSERMAN, ALDRICHIMICA ACTA, 20, 63 (1987). NEW METHODS IN THE FORMATION OF MONOCYCLIC LACTAMS AND LACTONES OF BIOLOGICAL INTERESTa
  162777. GABRIEL WEATHERHEAD
  162778. 9855N
  162779. 2/28/96VgA REVIEW. I. NITTA AND H. VENO, J. SYNTH. ORQ. CHEM., JPN., 45, 445 (1987). NEW SYNTHESES OF CORTICOIDSa
  162780. GABRIEL WEATHERHEAD
  162781. 9856N
  162782. 2/28/96V
  162783. A REVIEW. M.FUJITA AND T. HIYAMA, J. SYNTH. ORG. CHEM. JPN., 45, 664 (1987). NEW APPROACH TO SYNTHETIC PYRETHROIDS HAVING A TRIFLUOROMETHYL GROUPa
  162784. GABRIEL WEATHERHEAD
  162785. 9857N
  162786. 2/28/96
  162787. A REVIEW. P. KOVACIC AND M.B. JONES, CHEM. REV., 87, 357 (1987). DEHYDRO COUPLING OF AROMATIC NUCLEI BY CATALYST OXIDANT SYSTEMS: POLY(P PHENYLENE)a
  162788. GABRIEL WEATHERHEAD
  162789. 9858N
  162790. 2/28/96V
  162791. A REVIEW. N. MIZUNO AND M. MISONO, J. SYNTH.ORG.CHEM.JPN., 45, 258 (1987. SELECTIVE OXIDATION OF LOWER ALKANES OVER OXIDE CATALYSTSa
  162792. GABRIEL WEATHERHEAD
  162793. 9859N
  162794. 2/28/96VxA REVIEW. A.J. FATIADI, SYNTHESIS, 85 (1987). THE CLASSICAL PERMANGANATE ION: STILL A NOVEL OXIDANT IN ORGANIC CHEMISTRYa
  162795. GABRIEL WEATHERHEAD
  162796. 9860N
  162797. 2/28/96V
  162798. A REVIEW. G.A. SHVEKHGEIMER, V.I. ZVOLINSKII AND K.I. KOBRAKOV, CHEM. HETEROCYCL. COMPDS., 22, 353 (1986). SYNTHESIS OF HETEROCYCLES ON THE BASIS OF ALIPHATIC NITRO COMPOUNDSa
  162799. GABRIEL WEATHERHEAD
  162800. 9861N
  162801. 2/28/96V
  162802. A REVIEW. A.R. KATRITZKY, D.L. OSTERCAMP AND T.I. YOUSAF, TETRAHEDRON, 43, 5171 (1987). TETRAHEDRON REPORT 225: THE MECHANISMS OF HETEROCYCLIC RING CLOSURESa
  162803. GABRIEL WEATHERHEAD
  162804. 9862N
  162805. 2/28/96V
  162806. A REVIEW. L.Y. BREZHNEV, M.M. VARTANYAN, T.Y. SOLOV'EVA, V.A. ZETIROVA, N.P. KARZHAVINA AND R.A. KARAKHANOV, CHEM. HETEROCYCL. COMPDS., (ENGL. TRANSL.), 22, 931 (1986). SYNTHESIS AND PROPERTIES OF 1,6 DIOXASPIRO[4.4]NONANE AND ITS DERIVATIVESa
  162807. GABRIEL WEATHERHEAD
  162808. 9863N
  162809. 2/28/96VsA REVIEW. J.M. BOBBITT AND A.J. BOURQUE, HETEROCYCLES, 25, 601 (1987). SYNTHESIS OF HETEROCYCLES USING AMINOACETALSa
  162810. GABRIEL WEATHERHEAD
  162811. 9864N
  162812. 2/28/96V
  162813. A REVIEW. A. KAMAL AND P.B. SATTUR, HETEROCYCLES, 26, 1051 CHLOROSULFONYL ISOCYANATE: A NOVEL REAGENT FOR THE SYNTHESIS OF HETEROCYCLESa
  162814. GABRIEL WEATHERHEAD
  162815. 9865N
  162816. 2/28/96VqA REVIEW. J. TSUJI, HETEROCYCLES, 25, 1 (1987) CONTRIBUTIONS OF PROFESSOR GILBERT STORK IN HETEROCYCLIC CHEMISTRYa
  162817. GABRIEL WEATHERHEAD
  162818. 9866N
  162819. 2/28/96
  162820. VwA REVIEW. J. CHANET RAY AND R. VESSIERE, ORG.PREP. PROCED. INT., 8, 157 (1986). SYNTHESIS AND REACTIONS OF BETA SULTAMSa
  162821. GABRIEL WEATHERHEAD
  162822. 9867N
  162823. 2/28/96V
  162824. A REVIEW. K. TANAKA AND K. MITSUHASHI, J. SYNTH. ORG. CHEM. JPN., 45, 269 (1987) SYNTHESIS OF TRIFLUOROMETHYL AZOLES USING BUILDING BLOCKSa
  162825. GABRIEL WEATHERHEAD
  162826. 9868N
  162827. 2/28/96V
  162828. A REVIEW. Y. TAMARU AND Z. YOSHIDA, J. ORQANOMET. CHEM., 334, HETEROCYCLIC SYNTHESIS BY THE USE OF THE OXIDIZING POTENTIAL OF PALLADIUM (II)a
  162829. GABRIEL WEATHERHEAD
  162830. 9869N
  162831. 2/28/96V
  162832. A REVIEW. E. LUKEVITS AND I.D. SEGAL, CHEM. HETEROCYCL. COMPDS. (ENGL. TRANSL.), 23, 1 (1987). PYRIDYLSILANES IN THE SYNTHESIS OF HETEROCYCLESa
  162833. GABRIEL WEATHERHEAD
  162834. 9870N
  162835. 2/28/96V
  162836. A REVIEW. H. TAKAHATA AND T. YAMAZAKI, J. SYNTH. ORG. CHEM. JPN., 45, 682 (1987). SYNTHESIS OF HETEROCYCLES USING THIOAMIDE GROUPSa
  162837. GABRIEL WEATHERHEAD
  162838. 9871N
  162839. 2/28/96
  162840. A REVIEW. T. HIRAO AND Y. OHSHIRO, J. SYNTH. ORG. CHEM. JPN., 45, 784 (1987). SELECTIVE TRANSFORMATIONS OF FUNCTIONAL GROUPS BY USE OF DIALKYL PHOSPHONATESa
  162841. GABRIEL WEATHERHEAD
  162842. 9872N
  162843. 2/28/96V
  162844. A REVIEW. G.W. KABALKA, J. ORGANOMET. CHEM., 318, 1 (1987). BORON: BORANES IN ORGANIC SYNTHESIS. ANNUAL SURVEY COVERING THE YEAR 1984a
  162845. GABRIEL WEATHERHEAD
  162846. 9873N
  162847. 2/28/96V
  162848. A REVIEW. G.W. KABALKA, J. ORGANOMET. CHEM., 337, 169 (1987). BORON: BORANES IN ORGANIC SYNTHESIS. ANNUAL SURVEY COVERING THE YEAR 1985a
  162849. GABRIEL WEATHERHEAD
  162850. 9874N
  162851. 2/28/96VdA REVIEW. D.S. MATTESON, SYNTHESIS, 973 (1986). THE USE OF CHIRAL ORGANOBORANES IN ORGANIC SYNTHESISa
  162852. GABRIEL WEATHERHEAD
  162853. 9875N
  162854. 2/28/96VnA REVIEW. K. SMITH, CHEM. IND.(LONDON), 603 (1987). ADVANCES IN ORGANOBORON CHEMISTRY   PROSPECTS FOR INDUSTRYa
  162855. GABRIEL WEATHERHEAD
  162856. 9876N
  162857. 2/28/96
  162858. VpA REVIEW. H.C. BROWN AND J.V.N. VARA PRASAD, HETEROCYCLES, 25, 641 (1987). HYDROBORATION OF HETEROCYCLIC OLEFINSa
  162859. GABRIEL WEATHERHEAD
  162860. 9877N
  162861. 2/28/96V
  162862. A REVIEW. K. MULLEN, ANGEW. CHEM. INT. ED. ENGL., 26, 204 (1987). NEW REDUCTIVE TRANSFORMATIONS OF UNSATURATED CYCLIC HYDROCARBONSa
  162863. GABRIEL WEATHERHEAD
  162864. 9878N
  162865. 2/28/96VgA REVIEW. W.P. NEUMANN, SYNTHESIS, 665 (1987). TRI N BUTYLTIN HYDRIDE AS A REAGENT IN ORGANIC SYNTHESISa
  162866. GABRIEL WEATHERHEAD
  162867. 9879N
  162868. 2/28/96VdA REVIEW. J.M. BROWN, ANGEW. CHEM. INT. ED. ENQL., 26, 190 (1987). DIRECTED HOMOGENOUS HYDROGENATIONa
  162869. GABRIEL WEATHERHEAD
  162870. 9880N
  162871. 2/28/96VzA REVIEW. R.V. HOFFMAN, ORG. PREP. PROCED. INT., 18, 179 (1986). THE OXIDATION OF ELECTRON DONORS WITH SULPHONYL PEROXIDESa
  162872. GABRIEL WEATHERHEAD
  162873. 9881N
  162874. 2/28/96
  162875. A REVIEW. S.F. NELSEN, ACC. CHEM. RES., 20, 269 (1987). CATION RADICAL CATALYZED CHAIN OXYGENATION OF ALKYLATED OLEFINS AND DIENESa
  162876. GABRIEL WEATHERHEAD
  162877. 9882N
  162878. 2/28/96VfA REVIEW. P.G. BARALDI ET AL., SYNTHESIS, 52, 857 (1987). SYNTHESIS OF NATURAL PRODUCTS VIA ISOXAZOLESa
  162879. GABRIEL WEATHERHEAD
  162880. 9883N
  162881. 2/28/96V
  162882. A REVIEW. T.L.B. BOIVIN, TETRAHEDRON, 43, 3309 (1987). TETRAHEDRON REPORT. SYNTHETIC ROUTES TO TETRAHYDROFURAN, TETRAHYDROPYRAN AND SPIROKETAL UNITS OF POLYETHER ANTIBIOTICS AND A SURVEY OF SPIROKETALS OF OTHER NATURAL PRODUCTSa
  162883. GABRIEL WEATHERHEAD
  162884. 9884N
  162885. 2/28/96VqA REVIEW. D.M. GOODALL AND I.T. NORTON, ACC. CHEM. RES., 20, 59 (1987). POLYSACCHARIDE CONFORMATIONS AND KINETICSa
  162886. GABRIEL WEATHERHEAD
  162887. 9885N
  162888. 2/28/96V
  162889. A REVIEW. S.J. DANISHEFSKY AND M.P. DENINNO, ANGEW. CHEM. INT. ED. ENGL., 26, 15 (1987). TOTALLY SYNTHETIC ROUTES TO THE HIGHER MONOSACCHARIDESa
  162890. GABRIEL WEATHERHEAD
  162891. 9886N
  162892. 2/28/96V
  162893. A REVIEW. N.K. KOCHETKOV, TETRAHEDRON, 43, 2389 (1987). TETRAHEDRON REPORT 218: SYNTHESIS OF POLYSACCHARIDES WITH A REGULAR STRUCTUREa
  162894. GABRIEL WEATHERHEAD
  162895. 9887N
  162896. 2/28/96VuA REVIEW. J.W. HUFFMAN, TETRAHEDRON, 23, 5467 (1987). SYMPOSIA IN PRINT 30: CURRENT TOPICS IN SESQUITERPENE SYNTHESISa
  162897. GABRIEL WEATHERHEAD
  162898. 9888N
  162899. 2/28/96
  162900. A REVIEW. CHARPENTIER MORIZE, MICHELINE; BONNET DELPON, DANIELE. CARBOCATIONS DESTABILIZED BY ELECTRON WITHDRAWING GROUPS: APPLICATIONS IN ORGANIC SYNTHESIS. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.
  162901. GABRIEL WEATHERHEAD
  162902. 9889N
  162903. 2/28/96V
  162904. A REVIEW. OKAMOTO, KUNIO. GENERATION AND ION PAIR STRUCTURES OF UNSTABLE CARBOCATION INTERMEDIATES IN SOLVOLYTIC REACTIONS. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162905. GABRIEL WEATHERHEAD
  162906. 9890N
  162907. 2/28/96V
  162908. A REVIEW. RICHARD, JOHN P. SIMPLE RELATIONSHIPS BETWEEN CARBOCATION LIFETIME AND THE MECHANISM FOR NUCLEOPHILIC SUBSTITUTION AT SATURATED CARBON. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162909. GABRIEL WEATHERHEAD
  162910. 9891N
  162911. 2/28/96V
  162912. A REVIEW. KRAMER, GEORGE M., SCOUTEN, CHARLES G. THE 2 NORBORNYL CARBONIUM ION STABILIZING CONDITIONS: AN ASSESSMENT OF STRUCTURAL PROBES. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162913. GABRIEL WEATHERHEAD
  162914. 9892N
  162915. 2/28/96V
  162916. A REVIEW. CREARY, XAVIER; HOPKINSON, ALAN C.; LEE RUFF, EDWARD. A CARBONYL CATIONS. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162917. GABRIEL WEATHERHEAD
  162918. 9893N
  162919. 2/28/96
  162920. A REVIEW. ALLEN, ANNETTE D.; TIDWELL, THOMAS T. FLUORINE SUBSTITUTED CARBOCATIONS. ADVANCES IN CARBOCATION CHEMISTRY. VOLUME 1, XAVIER CREARY, ED., JAI PRESS, INC.: GREENWICH, CT, 1989.a
  162921. GABRIEL WEATHERHEAD
  162922. 9894N
  162923. 2/28/96V
  162924. A REVIEW. OARE, DAVID A., HEATHCOCK, CLAYTON H. STEREOCHEMISTRY OF THE BASE PROMOTED MICHAEL ADDITION REACTION. 1989,19, 227 407. TOPICS IN STEREOCHEMISTRYa
  162925. GABRIEL WEATHERHEAD
  162926. 9895N
  162927. 2/28/96V
  162928. A REVIEW. SCOTT, JOHN W. ENANTIOSELECTIVE SYNTHESIS OF NON RACEMIC CHIRAL MOLECULES ON AN INDUSTRIAL SCALE. 1989,19, 209 26. TOPICS IN STEREOCHEMISTRYa
  162929. GABRIEL WEATHERHEAD
  162930. 9896N
  162931. 2/28/96V
  162932. A REVIEW. BENNER, STEVEN A., GLASFELD, ARTHUR, PICCIRILLI, JOSEPH A. STEREOSPECIFICITY IN ENZYMOLOGY: ITS PLACE IN EVOLUTION. 1989, 19, 127 207. TOPICS IN STEREOCHEMISTRYa
  162933. GABRIEL WEATHERHEAD
  162934. 9897N
  162935. 2/28/96
  162936. A REVIEW. SIH, CHARLES, J.; WU, SHIH HSIUNG. RESOLUTION OF ENANTIOMERS VIA BIOCATALYSIS. 1989,19, 63 125. TOPICS IN STEREOCHEMISTRYa
  162937. GABRIEL WEATHERHEAD
  162938. 9898N
  162939. 2/28/96V
  162940. A REVIEW. FACELLI, JULIO C.; GRANT, DAVID M. MOLECULAR STRUCTURE AND CARBON 13 CHEMICAL SHIELD TENSORS OBTAINED FROM NUCLEAR MAGNETIC RESONANCE. 1989,19,1 61. TOPICS IN STEREOCHEMISTRYa
  162941. GABRIEL WEATHERHEAD
  162942. 9899N
  162943. 2/28/96
  162944. +A REVIEW. CLOUTHIER, DENNIS J.; MOULE, DAVID C. PERIODIC GROUP RELATIONSHIPS IN THE SPECTROSCOPY OF THE CARBONYLS, KETENES, AND NITRILES: THE EFFECT OF SUBSTITUTION BY SULFUR, SELENIUM AND PHOSPHORUS. 1989,150 (RELATIONSHIPS AND MECHANISMS IN THE PERIODIC TABLE), 167 247 TOPICS IN CURRENT CHEMISTRY
  162945. GABRIEL WEATHERHEAD
  162946. 9900N
  162947. 2/28/96
  162948. A REVIEW. TORII, SIGERU; TANAKA, HIDEO; INOKUCHI, TSUTOMU. ROLE OF THE ELECTROCHEMICAL METHOD IN THE TRANSFORMATION OL B LACTAM ANTIBIOTICS AND TERPENOIDS. 1988, 148(ELECTROCHEMISTRY 3), 153 94. TOPICS IN CURRENT CHEMISTRYa
  162949. GABRIEL WEATHERHEAD
  162950. 9901N
  162951. 2/28/96V
  162952. A REVIEW. SHONO, TATSUYA. SYNTHESIS OF ALKALOIDAL COMPOUNDS USING AN ELECTROCHEMICAL REACTION AS A KEY STEP. 1988, 148 (ELECTROCHEMISTRY 3), 131 51. TOPICS IN CURRENT CHEMISTRYa
  162953. GABRIEL WEATHERHEAD
  162954. 9902N
  162955. 2/28/96V
  162956. A REVIEW. DEVLIN, JOHN P.; HARGRAVE, KARL D. THE DESIGN AND SYNTHESIS OF IMMUNE REGULATORY AGENTS: TARGETS AND APPROACHES. 1989, 45(14), 4327 69. TETRAHEDRONa
  162957. GABRIEL WEATHERHEAD
  162958. 9903N
  162959. 2/28/96V|A REVIEW. BERNASCONI, CLAUDE F. NUCLEOPHILIC ADDITION TO OLEFINS. KINETICS AND MECHANISM. 1989, 45(13), 4017 90. TETRAHEDRONa
  162960. GABRIEL WEATHERHEAD
  162961. 9904N
  162962. 2/28/96
  162963. A REVIEW. BOYKIN, DAVID W., BAUMSTARK, ALFONS L. OXYGEN 17 NMR SPECTROSCOPY: ASSESSMENT OF STERIC PERTURBATION OF STRUCTURE IN ORGANIC COMPOUNDS. 1989, 45(12), 3613 53. TETRAHEDRONa
  162964. GABRIEL WEATHERHEAD
  162965. 9905N
  162966. 2/28/96VcA REVIEW. MORI, KENJI. SYNTHESIS OF OPTICALLY ACTIVE PHEROMONES. 1989, 45(11), 3233 98. TETRAHEDRONa
  162967. GABRIEL WEATHERHEAD
  162968. 9906N
  162969. 2/28/96V
  162970. A REVIEW. TAMM, CHRISTOPH; JEKER, NICOLAS. SYNTHESIS OF MACROCYCLIC TRICHOTHECENE MYCOTOXINS. 1989, 45(8), 2385 415. TETRAHEDRONa
  162971. GABRIEL WEATHERHEAD
  162972. 9907N
  162973. 2/28/96VtA REVIEW. ZAMIR, LOLITA O. BIOSYNTHESIS OF 3 ACETYLDEOXYNIVALENOL AND SAMBUCINOL. 1989, 45(8), 2277 305. TETRAHEDRONa
  162974. GABRIEL WEATHERHEAD
  162975. 9908N
  162976. 2/28/96V|A REVIEW. MORGAN, MICHAEL R. A. MYCOTOXIN IMMUNOASSAYS (WITH SPECIAL REFERENCE TO ELISAS). 1989, 45(8), 2237 49. TETRAHEDRONa
  162977. GABRIEL WEATHERHEAD
  162978. 9909N
  162979. 2/28/96
  162980. 9VkA REVIEW. MATTESON, DONALD S. BORONIC ESTERS IN STEREODIRECTED SYNTHESIS. 1989, 45(7), 1859 85. TETRAHEDRONa
  162981. GABRIEL WEATHERHEAD
  162982. 9910N
  162983. 2/28/96VqA REVIEW. RABIDEAU, PETER W. THE METAL AMMONIA REDUCTION OF AROMATIC COMPOUNDS. 1989, 45(6),1579 603. TETRAHEDRONa
  162984. GABRIEL WEATHERHEAD
  162985. 9911N
  162986. 2/28/96V
  162987. A REVIEW. HWU, JIH RU; GILBERT, BRYANT A. COUNTERATTACK REAGENTS IN ORGANIC REACTIONS AND IN SYNTHESES. 1989, 45(5),1233 61. TETRAHEDRONa
  162988. GABRIEL WEATHERHEAD
  162989. 9912N
  162990. 2/28/96V
  162991. A REVIEW. NEUMANN WILHELM P. HILLGAERTNER, HORST, BAINES, KIM M.; DICKE, RITA; VORSPOHL, KLAUS; KOBS, UWE; NUSSBEUTEL, UDO. NEW WAYS OF GENERATING ORGANOTIN REACTIVE INTERMEDIATES FOR ORGANIC SYNTHESIS. 1989, 45(4), 951 60. TETRAHEDRONa
  162992. GABRIEL WEATHERHEAD
  162993. 9913N
  162994. 2/28/96
  162995. A REVIEW. BUCHANAN, GERALD W. APPLICATIONS OF NITROGEN 15 NMR SPECTROSCOPY TO THE STUDY OF MOLECULAR STRUCTURE, STEREOCHEMISTRY AND BINDING PHENOMENA. 1989, 45(3), 581 604. TETRAHEDRONa
  162996. GABRIEL WEATHERHEAD
  162997. 9914N
  162998. 2/28/96V
  162999. A REVIEW. RABINOVITZ, MORDECAI; COHEN, YORAM. PROBING THE NATURE OF POLYCYCLIC CONJUGATED DIANIONS. FROM CARBOCYCLIC TO HETEROCYCLIC DIANIONS. NMR STUDIES, P DELOCALIZATION AND ELECTRON STRUCTURE. 1988, 44(23), 6957 94. TETRAHEDRONa
  163000. GABRIEL WEATHERHEAD
  163001. 9915N
  163002. 2/28/96VfA REVIEW. ANAND, NITYA; SINGH, JUJHAR. CHEMISTRY OF LACTAM ACETALS. 1988, 44(19), 5975 99. TETRAHEDRONa
  163003. GABRIEL WEATHERHEAD
  163004. 9916N
  163005. 2/28/96V
  163006. A REVIEW. BARRETT, ANTHONY G. M.; STURGESS, MICHAEL A. APPLICATIONS OF ORGANOMETALLIC REAGENTS IN B LACTAM CHEMISTRY. 1988, 44(18), 5615 52. TETRAHEDRONa
  163007. GABRIEL WEATHERHEAD
  163008. 9917N
  163009. 2/28/96
  163010. AVuA REVIEW. MARUOKA, KEIJI; YAMAMOTO, HISASHI. ORGANOALUMINUMS IN ORGANIC SYNTHESIS. 1988, 44(16), 5001 32. TETRAHEDRONa
  163011. GABRIEL WEATHERHEAD
  163012. 9918N
  163013. 2/28/96VxA REVIEW. FRAUENRATH, HERBERT. VINYL ACETALS AND RELATED COMPOUNDS IN ORGANIC SYNTHESIS. 1989, NO. 10, 721 34. SYNTHESISa
  163014. GABRIEL WEATHERHEAD
  163015. 9919N
  163016. 2/28/96VkA REVIEW. FUERSTNER, ALOIS. RECENT ADVANCEMENTS IN THE REFORMATSKY REACTION. 1989, NO. 8, 571 90. SYNTHESISa
  163017. GABRIEL WEATHERHEAD
  163018. 9920N
  163019. 2/28/96VmA REVIEW. SHARMA, SATYAVAN. ISOTHIOCYANATES IN HETEROCYCLIC SYNTHESIS. 5. 1989, 8(5), 327 469. SULFUR REPORTSa
  163020. GABRIEL WEATHERHEAD
  163021. 9921N
  163022. 2/28/96V
  163023. A REVIEW. KATO, SHINZI; ISHIDA, MASARU. ACYCLIC DITHIOCARBOXYLIC ACID ESTERS
  163024. REACTIONS AND SYNTHESES. 1988, 8(4),155 312. SULFUR REPORTSa
  163025. GABRIEL WEATHERHEAD
  163026. 9922N
  163027. 2/28/96
  163028. A REVIEW. BECHER, JAN, STIDSEN, CARSTEN E. RECENT DEVELOPMENTS IN THE SYNTHESIS AND CHEMISTRY OF 2(1H) PYRIDINETHIONES AND RELATED COMPOUNDS. 1988, 8(3),105 146. SULFUR REPORTSa
  163029. GABRIEL WEATHERHEAD
  163030. 9923N
  163031. 2/28/96V
  163032. A REVIEW. NADDAKA, V. I.; SADEKOV, I. D.; MAKSIMENKO, A. A.; MINKIN, V. I. P TELLURANES: SYNTHESIS, STRUCTURE AND REACTIVITY. 1988, 8(2), 61 100. SULFUR REPORTSa
  163033. GABRIEL WEATHERHEAD
  163034. 9924N
  163035. 2/28/96V
  163036. A REVIEW. CHIMIAK,ANDRZEJ ,MILEWSKA MARIAJ. N HYDROXYAMINOACIDS AND THEIR DERIVATIVES 1988, 53, 203 77 PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  163037. GABRIEL WEATHERHEAD
  163038. 9925N
  163039. 2/28/96V
  163040. A REVIEW. CHA, JIN SOON. RECENT DEVELOPMENTS IN THE SYNTHESIS OF ALDEHYDES BY REDUCTION OF CARBOXYLIC ACIDS AND THEIR DERIVATIVES WITH METAL HYDRIDES. 1989, 21(4), 451 77. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163041. GABRIEL WEATHERHEAD
  163042. 9926N
  163043. 2/28/96
  163044. A REVIEW. FETZER, JOHN C. SYNTHESIS OF LARGE CONDENSED POLYCYCLIC AROMATIC HYDROCARBONS. 1989, 21(1), 47 65. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163045. GABRIEL WEATHERHEAD
  163046. 9927N
  163047. 2/28/96V
  163048. A REVIEW. LOWN, J. WILLIAM. SYNTHETIC CHEMISTRY OF NATURALLY OCCURRING OLIGOPEPTIDE ANTIBIOTICS AND RELATED LEXITROPSINS. 1989, 21(1), 1 46. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163049. GABRIEL WEATHERHEAD
  163050. 9928N
  163051. 2/28/96V
  163052. A REVIEW. POIRIER, JEAN MARIE. SYNTHESIS AND REACTIONS OF FUNCTIONALIZED SILYL ENOL ETHERS. 1988, 20(4), 317 69. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163053. GABRIEL WEATHERHEAD
  163054. 9929N
  163055. 2/28/96V
  163056. A REVIEW. USON, RAFAEL, USON, MIGUEL A. SYNTHETIC APPROACHES TO HOMO  OR HETEROPOLYNUCLEAR PENTAHALOPHENYL PALLADIUM(II) OR PLATINUM(II) COMPLEXES. 1988,12(6 7), 707 13. NEW JOURNAL OF CHEMISTRYa
  163057. GABRIEL WEATHERHEAD
  163058. 9930N
  163059. 2/28/96
  163060. A REVIEW. SAPPA, ENRICO; TIRIPICCHIO, ANTONIO. A TEN YEAR STROLL IN THE CHEMISTRY OF NICKEL CONTAINING HETEROMETALLIC CLUSTERS OF THE IRON TRIAD. SYNTHESIS, STRUCTURE, AND CATALYTIC ACTIVITY. 1988, 12(6 7), 599 611. NEW JOURNAL OF CHEMISTRYa
  163061. GABRIEL WEATHERHEAD
  163062. 9931N
  163063. 2/28/96
  163064. KA REVIEW. ELSEVIER, C. J.; MULLER, F.; VRIEZE, K.; ZOET, R. SITE SELECTIVITY AND CRUCIAL INTERMEDIATES IN THE REACTIONS OF HOMO  AND HETERO BIMETALLIC COMPOUNDS MM'(C0)6(IPRN:C(H)C(H):N I PR) (M = M' = FE, RU; M = FE, M' = RU) WITH MOLECULAR HYDROGEN (MOLECULAR DEUTERIUM) AND ALKYNES. 1988,12(6 7), 571 9. NEW JOURNAL OF CHEMISTRY
  163065. GABRIEL WEATHERHEAD
  163066. 9932N
  163067. 2/28/96V
  163068. A REVIEW. FUNAYAMA, S.; CORDELL, G. A. POLYMERIZATION AND/OR REARRANGEMENT REACTIONS OF ACRONYCINE AND RELATED COMPOUNDS. 1989, 29(4), 815 37. HETEROCYCLESa
  163069. GABRIEL WEATHERHEAD
  163070. 9933N
  163071. 2/28/96
  163072. QVuA REVIEW. GOL'DBERG, YU.; STURKOVICH, R.; LUKEVICS, E. HETEROCYCLIC SONOCHEMISTRY. 1989, 29(3), 597 627. HETEROCYCLESa
  163073. GABRIEL WEATHERHEAD
  163074. 9934N
  163075. 2/28/96VSA REVIEW. SILWA, W. N SUBSTITUTED PYRIDINIUM SALTS. 1989, 29(3) 557 95 HETEROCYCLESa
  163076. GABRIEL WEATHERHEAD
  163077. 9935N
  163078. 2/28/96V
  163079. A REVIEW. MICHALSKA, MARIA, MICHALSKI, JAN. GLYCOSYL THIO , AND SELENO  AND TELLUROPHOSPHATES. 1989, 28(2),1249 56. HETEROCYCLESa
  163080. GABRIEL WEATHERHEAD
  163081. 9936N
  163082. 2/28/96
  163083. A REVIEW. HIRAMA, MASAHIRO; ITO, SHO. ASYMMETRIC INDUCTION IN THE INTRAMOLECULAR CONJUGATE ADDITION OF G  OR D CARBAMOYLOXY  A,B  UNSATURATED ESTERS. A NEW METHOD FOR DIASTEREOSELECTIVE AMINATION AND DIVERGENT SYNTHESIS OF 3 AMINO2,3,6 TRIDEOXYHEXOSES. 1989, 28(2), 1229 47. HETEROCYCLES
  163084. GABRIEL WEATHERHEAD
  163085. 9937N
  163086. 2/28/96
  163087. A REVIEW. KRIEF, A., DUMONT, W., VAN, E. D., HALAZY, S., LABAR D.; LABOUREUR, J. L.; LE, T. Q. ORIGINAL SYNTHESES OF EPOXIDES INVOLVING ORGANOSELENIUM INTERMEDIATES. 1989, 28(2), 1203 28 HETEROCYCLESa
  163088. GABRIEL WEATHERHEAD
  163089. 9938N
  163090. 2/28/96V
  163091. A REVIEW. SCOTT, A. IAN. APPLICATIONS OF NMR AND MOLECULAR BIOLOGY IN STUDIES OF THE ENZYME MECHANISMS OF VITAMIN BL2 BIOSYNTHESIS. 1989, 28(2), 1193 201. HETEROCYCLESa
  163092. GABRIEL WEATHERHEAD
  163093. 9939N
  163094. 2/28/96V
  163095. A REVIEW. GONZALEZ, ANTONIO G.; GALINDO, A.; MANSILLA, H. BIOMIMETIC TRANSFORMATIONS OF SESQUITERPENE LACTONES. 1989 28(1), 529 45. HETEROCYCLESa
  163096. GABRIEL WEATHERHEAD
  163097. 9940N
  163098. 2/28/96V
  163099. A REVIEW. FETIZON, MARCEL, GOULAOUIC, PIERRE HANNA, ISSAM. THE CHEMISTRY OF 1,4 DIOXENE (2,3 DIHYDRO 1,4DIOXIN). PART VIII. 1989, 28(1), 521 7. HETEROCYCLESa
  163100. GABRIEL WEATHERHEAD
  163101. 9941N
  163102. 2/28/96
  163103. A REVIEW. MINISCI, FRANCESCO, VISMARA, ELENA, FONTANA, FRANCESCA. RECENT DEVELOPMENTS OF FREE RADICAL SUBSTITUTIONS OF HETEROAROMATIC BASES. 1989, 28(1), 489 519. HETEROCYCLESa
  163104. GABRIEL WEATHERHEAD
  163105. 9942N
  163106. 2/28/96V
  163107. A REVIEW. BROSSI, ARNOLD. RESEARCH ON BIOACTIVE NATURAL PRODUCTS AT THE NATIONAL INSTITUTES OF HEALTH (1976 1988). 1988 27(12), 2905 11. HETEROCYCLESa
  163108. GABRIEL WEATHERHEAD
  163109. 9943N
  163110. 2/28/96V
  163111. A REVIEW. SAKATA, GOZYO; MAKINO, KENJI; KURASAWA, YOSHIHISA. RECENT PROGRESS IN THE QUINOXALINE CHEMISTRY. SYNTHESIS AND BIOLOGICAL ACTIVITY. 1988, 27(10), 2481 515. HETEROCYCLESa
  163112. GABRIEL WEATHERHEAD
  163113. 9944N
  163114. 2/28/96V
  163115. A REVIEW. ALPEGIANI, MARCO; BEDESCHI, ANGELO; PERRONE, ETTORE; ZARINI, FRANCO, FRANCHESCHI, GIOVANNI. 2 (HETEROATOMSUBSTITUTED)METHYL PENEMS. III. NITROGEN DERIVATIVES. 1988, 27(6), 1329 40. HETEROCYCLESa
  163116. GABRIEL WEATHERHEAD
  163117. 9945N
  163118. 2/28/96
  163119. ]VsA REVIEW. KRECHL, JIRI; CASTULIK, PAVEL. ENZYME MODELS BASED ON CYCLODEXTRIN. 1989, 29(2), 173 80.  CHEMICA SCRIPTAa
  163120. GABRIEL WEATHERHEAD
  163121. 9946N
  163122. 2/28/96V
  163123. A REVIEW. LEMMEN, PETER; BAUMGARTNER, REGINA; UGI, LVAR; RAMIREZ, FAUSTO. THE DEFORMATION OF THE PHOSPHORANE SKELETON AS EVIDENCE FOR REORGANIZATION PATHWAYS. 1988, 28(4), 451 64. CHEMICA SCRIPTAa
  163124. GABRIEL WEATHERHEAD
  163125. 9947N
  163126. 2/28/96V
  163127. A REVIEW. NOYORI, R. CHEMICAL MULTIPLICATION OF CHIRALITY: SCIENCE AND APPIICATIONS. 1989,18(2),187 208. CHEMICAL SOCIETY REVIEWSa
  163128. GABRIEL WEATHERHEAD
  163129. 9948N
  163130. 2/28/96V
  163131. A REVIEW. GORDON, ISABEL M.; MASKILL, H.; RUASSE, MARIE FRANCOISE. SULFONYL TRANSFER REACTIONS. 1989,18(2),123 61. CHEMICAL SOCIETY REVIEWSa
  163132. GABRIEL WEATHERHEAD
  163133. 9949N
  163134. 2/28/96V
  163135. A REVIEW. BILLINGTON, DAVID C. RECENT DEVELOPMENTS IN THE SYNTHESIS OF MYO INOSITOL PHOSPHATES. 1989,18(1), 83 122. CHEMICAL SOCIETY REVIEWSa
  163136. GABRIEL WEATHERHEAD
  163137. 9950N
  163138. 2/28/96VlA REVIEW. PATON, R. MICHAEL. THE CHEMISTRY OF NITRILE SULFIDES. 1989, 18(1), 33 52. CHEMICAL SOCIETY REVIEWSa
  163139. GABRIEL WEATHERHEAD
  163140. 9951N
  163141. 2/28/96V`A REVIEW. MASON,STEPHEN. BIOMOLECULARHOMOCHIRALITY. 1988,17(4), 347 59. CHEMICAL SOCIETY REVIEWSa
  163142. GABRIEL WEATHERHEAD
  163143. 9952N
  163144. 2/28/96V
  163145. A REVIEW. PATTENDEN, GERALD. COBALT MEDIATED RADICAL REACTIONS IN ORGANIC SYNTHESIS. 1988, 17(4), 361 82. CHEMICAL SOCIETY REVIEWSa
  163146. GABRIEL WEATHERHEAD
  163147. 9953N
  163148. 2/28/96VvA REVIEW. GOLDSCHMIDT, Z.; CRAMMER, B. VINYLCYCLOPROPANE REARRANGEMENTS. 1988, 17(3), 229 67. CHEMICAL SOCIETY REVIEWSa
  163149. GABRIEL WEATHERHEAD
  163150. 9954N
  163151. 2/28/96V
  163152. A REVIEW. BOWMAN, W. R. REACTIVITY OF SUBSTITUTED ALIPHATIC NITRO COMPOUNDS WITH NUCLEOPHILES. 1988,17(3), 283 316. CHEMICAL SOCIETY REVIEWSa
  163153. GABRIEL WEATHERHEAD
  163154. 9955N
  163155. 2/28/96
  163156. A REVIEW. BLACKBURN, BRENT K.; DAVIES, STEPHEN G.; SUTTON, KEVIN H.; WHITTAKER, MARK. A CONFORMATIONAL ANALYSIS OF TRANSITION METAL  1  ACYL COMPLEXES: STERIC INTERACTIONS AND STEREOELECTRONIC EFFECTS. 1988,17(2), 147 79. CHEMICAL SOCIETY REVIEWSa
  163157. GABRIEL WEATHERHEAD
  163158. 9956N
  163159. 2/28/96V
  163160. A REVIEW. BRAUNSTEIN, PIERRE NOBEL, DOMINIQUE. TRANSITIONMETAL MEDIATED REACTIONS OF ORGANIC ISOCYANATES. 1927, 89(8), 1927 45. CHEMICAL REVIEWSa
  163161. GABRIEL WEATHERHEAD
  163162. 9957N
  163163. 2/28/96V
  163164. A REVIEW. HOFFMANN, REINHARD W. ALLYLIC 1,3 STRAIN AS A CONTROLLING FACTOR IN STEREOSELECTIVE TRANSFORMATIONS. 1989, 89(8), 184 1 60. CHEMICAL REVIEWSa
  163165. GABRIEL WEATHERHEAD
  163166. 9958N
  163167. 2/28/96V
  163168. A REVIEW. WELTNER, WILLIAM, JR.; VAN ZEE, RICHARD J. CARBON MOLECULES, IONS, AND CLUSTERS. 1989, 89(8), 1713 47. CHEMICAL REVIEWSa
  163169. GABRIEL WEATHERHEAD
  163170. 9959N
  163171. 2/28/96
  163172. A REVIEW. ADAMS, RICHARD D. METAL CLUSTER COMPLEXES CONTAINING HETEROATOM SUBSTITUTED CARBENE LIGANDS. 1989, 89(8), 1703 12. CHEMICAL REVIEWSa
  163173. GABRIEL WEATHERHEAD
  163174. 9960N
  163175. 2/28/96V
  163176. A REVIEW. ALLEN, MARY TEDD, WHITTEN DAVID G. THE PHOTOPHYSICS AND PHOTOCHEMISTRY OF A,W DIPHENYLPOLYENE SINGLET STATES. 1989, 89(8), 1691 702. CHEMICAL REVIEWSa
  163177. GABRIEL WEATHERHEAD
  163178. 9961N
  163179. 2/28/96V
  163180. A REVIEW. PINDUR, ULF; ERFANIAN ABDOUST, HOUSHANG. INDOLO 2,3 QUINODIMETHANES AND STABLE CYCLIC ANALOGS FOR REGIO  AND STEREOCONTROLLED SYNTHESES OF [B] ANNELATED INDOLES. 1989 89(8), 1681 9. CHEMICAL REVIEWSa
  163181. GABRIEL WEATHERHEAD
  163182. 9962N
  163183. 2/28/96V
  163184. A REVIEW. BLYSTONE, SHERI L. SYNTHETIC APPLICATIONS OF ENANTIOSELECTIVE ORGANOTRANSITION METAL MEDIATED REACTIONS. 1989, 89(8), 1663 79. CHEMICAL REVIEWSa
  163185. GABRIEL WEATHERHEAD
  163186. 9963N
  163187. 2/28/96
  163188. oVmA REVIEW. PERRON, FRANCOISE ALBIZATI, KIM F. CHEMISTRY OF SPIROKETALS. 1989, 89(7), 1617 61. CHEMICAL REVIEWSa
  163189. GABRIEL WEATHERHEAD
  163190. 9964N
  163191. 2/28/96V
  163192. A REVIEW. HWU, JIH RU, WANG, NAELONG. STERIC INFLUENCE OF THE TRIMETHYLSILYL GROUP IN ORGANIC REACTIONS. 1989, 89(7), 1599 615. CHEMICAL REVIEWSa
  163193. GABRIEL WEATHERHEAD
  163194. 9965N
  163195. 2/28/96V
  163196. A REVIEW. KRAUS, GEORGE A., HON, YUN SON; THOMAS, P. J.; LARAMAY STEVE; LIRAS, SPIROS; HANSON, JEFF. ORGANIC SYNTHESIS USING BRIDGEHEAD CARBOCATIONS AND BRIDGEHEAD ENONES. 1989 89(7), 1591 8. CHEMICAL REVIEWSa
  163197. GABRIEL WEATHERHEAD
  163198. 9966N
  163199. 2/28/96VjA REVIEW. WHITESELL, JAMES K. C2 SYMMETRY AND ASYMMETRIC INDUCTION. 1989, 89(7), 1581 90. CHEMICAL REVIEWSa
  163200. GABRIEL WEATHERHEAD
  163201. 9967N
  163202. 2/28/96V
  163203. A REVIEW. MILLER, MARVIN J. SYNTHESIS AND THERAPEUTIC POTENTIAL OF HYDROXAMIC ACID BASED SIDEROPHORES AND ANALOGS. 1989, 89(7), 1563 79. CHEMICAL REVIEWSa
  163204. GABRIEL WEATHERHEAD
  163205. 9968N
  163206. 2/28/96VsA REVIEW. MIDLAND, M. MARK. ASYMMETRIC REDUCTIONS WITH ORGANOBORANE REAGENTS. 1989, 89(7),1553 61. CHEMICAL REVIEWSa
  163207. GABRIEL WEATHERHEAD
  163208. 9969N
  163209. 2/28/96V
  163210. A REVIEW. MATTESON, DONALD S. ALPHA HALO BORONIC ESTERS: INTERMEDIATES FOR STEREODIRECTED SYNTHESIS. 1989, 89(7), 1535 51. CHEMICAL REVIEWSa
  163211. GABRIEL WEATHERHEAD
  163212. 9970N
  163213. 2/28/96V
  163214. A REVIEW. WEINREB, STEVEN M., SCOLA, PAUL M. N ACYL IMINES AND RELATED HETERO DIENES IN [4+2] CYCLOADDITION REACTIONS. 1989, 89(7), 1525 34. CHEMICAL REVIEWSa
  163215. GABRIEL WEATHERHEAD
  163216. 9971N
  163217. 2/28/96VwA REVIEW. MCMURRY, JOHN E. CARBONYL COUPLING REACTIONS USING LOW VALENT TITANIUM. 1989, 89(7),1513 24. CHEMICAL REVIEWSa
  163218. GABRIEL WEATHERHEAD
  163219. 9972N
  163220. 2/28/96V|A REVIEW. MARSHALL, JAMES A. SN2' ADDITIONS OF ORGANOCOPPER REAGENTS TO VINYLOXIRANES. 1989, 89(7) 1503 11. CHEMICAL REVIEWSa
  163221. GABRIEL WEATHERHEAD
  163222. 9973N
  163223. 2/28/96
  163224. yVuA REVIEW. FINET, JEAN PIERE. ARYLATION REACTIONS WITH ORGANOBISMUTH REAGENTS. 1989, 89(7), 1487 501. CHEMICAL REVIEWSa
  163225. GABRIEL WEATHERHEAD
  163226. 9974N
  163227. 2/28/96V
  163228. A REVIEW. HUDLICKY, TOMAS; PRICE, JOHN D. ANIONIC APPROACHES TO THE CONSTRUCTION OF CYCLOPENTANOIDS. 1989, 89(7), 1467 86. CHEMICAL REVIEWSa
  163229. GABRIEL WEATHERHEAD
  163230. 9975N
  163231. 2/28/96V
  163232. A REVIEW. HART, DAVID J.; HA, DEOK CHAN. THE ESTER ENOLATE IMINE CONDENSATION ROUTE TO B LACTAMS. 1989, 89(7), 1447 65. CHEMICAL REVIEWSa
  163233. GABRIEL WEATHERHEAD
  163234. 9976N
  163235. 2/28/96V
  163236. A REVIEW. DAVES, G. DOYLE, JR.; HALLBERG, ANDERS. 1,2 ADDITIONS TO HETEROATOM SUBSTITUTED OLEFINS BY ORGANOPALLADIUM REAGENTS. 1989, 89(7),1433 45. CHEMICAL REVIEWSa
  163237. GABRIEL WEATHERHEAD
  163238. 9977N
  163239. 2/28/96V
  163240. A REVIEW. CRICH, DAVID; QUINTERO, LETICIA. RADICAL CHEMISTRY ASSOCIATED WITH THE THIOCARBONYL GROUP. 1989, 89(7),1413 32. CHEMICAL REVIEWSa
  163241. GABRIEL WEATHERHEAD
  163242. 2/28/96V`A REVIEW. SALAUN, JACQUES. OPTICALLY ACTIVE CYCLOPROPANES. 1989 89(5), 1247 70. CHEMICAL REVIEWSa
  163243. GABRIEL WEATHERHEAD
  163244. 9979N
  163245. 2/28/96VdA REVIEW. ALDER, ROGER W. STRAIN EFFECTS ON AMINE BASICITIES. 1989, 89(5), 1215 23. CHEMICAL REVIEWSa
  163246. GABRIEL WEATHERHEAD
  163247. 9980N
  163248. 2/28/96V~A REVIEW. TOCHTERMANN WERNER, OLSSON, GESA. 3 HETEROQUADRICYCLANES IN ORGANIC SYNTHESIS. 1989, 89(5),1203 14. CHEMICAL REVIEWSa
  163249. GABRIEL WEATHERHEAD
  163250. 9981N
  163251. 2/28/96VlA REVIEW. MURRAY, ROBERT W. CHEMISTRY OF DIOXIRANES. 12. DIOXIRANES. 1989, 89(5), 1187 201. CHEMICAL REVIEWSa
  163252. GABRIEL WEATHERHEAD
  163253. 9982N
  163254. 2/28/96ViA REVIEW. HALTON, BRIAN. DEVELOPMENTS IN CYCLOPROPARENE CHEMISTRY. 1989, 89(5), 1161 85. CHEMICAL REVIEWSa
  163255. GABRIEL WEATHERHEAD
  163256. 9983N
  163257. 2/28/96VxA REVIEW. BILLUPS, W. E.; HALEY, MICHAEL M.; LEE, GON ANN. BICYCLO[N.1.0]ALKENES. 1989, 89(5), 1147 59. CHEMICAL REVIEWSa
  163258. GABRIEL WEATHERHEAD
  163259. 9984N
  163260. 2/28/96V
  163261. A REVIEW. HASSENRUCK, KARIN; MARTIN, HANS DIETER; WALSH, ROBIN. CONSEQUENCES OF STRAIN IN (CH)8 HYDROCARBONS. 1989, 89(5), 1125 46. CHEMICAL REVIEWSa
  163262. GABRIEL WEATHERHEAD
  163263. 9985N
  163264. 2/28/96V_A REVIEW. JOHNSON, RICHARD P. STRAINED CYCLIC CUMULENES. 1989, 89(5), 1111 24. CHEMICAL REVIEWSa
  163265. GABRIEL WEATHERHEAD
  163266. 9986N
  163267. 2/28/96VaA REVIEW. BORDEN, WESTON THATCHER. PYRAMIDALIZED ALKENES. 1989, 89(5), 1095 109. CHEMICAL REVIEWSa
  163268. GABRIEL WEATHERHEAD
  163269. 9987N
  163270. 2/28/96VdA REVIEW. WARNER, PHILIP M. STRAINED BRIDGEHEAD DOUBLE BONDS. 1989, 89(5), 1067 93. CHEMICAL REVIEWSa
  163271. GABRIEL WEATHERHEAD
  163272. 9988N
  163273. 2/28/96VpA REVIEW. PAQUETTE, LEO A. DODECAHEDRANES AND ALLIED SPHERICAL MOLECULES. 1989, 89(5), 1051 65. CHEMICAL REVIEWSa
  163274. GABRIEL WEATHERHEAD
  163275. 9989N
  163276. 2/28/96
  163277. A REVIEW. KLUNDER, A. J. H.; ZWANENBURG, B. STRAINED BRIDGEHEAD CAGE ALCOHOLS AND DERIVATIVES. 1989, 89(5),1035 50. CHEMICAL REVIEWSa
  163278. GABRIEL WEATHERHEAD
  163279. 9990N
  163280. 2/28/96V
  163281. A REVIEW. MARCHAND, ALAN P. SYNTHESIS AND CHEMISTRY OF HOMOCUBANES, BISHOMOCUBANES, AND TRISHOMOCUBANES. 1989, 89(5), 1011 33. CHEMICAL REVIEWSa
  163282. GABRIEL WEATHERHEAD
  163283. 9991N
  163284. 2/28/96VxA REVIEW. GRIFFIN, GARY W.; MARCHAND, ALAN P. SYNTHESIS AND CHEMISTRY OF CUBANES. 1989, 89(5) 997 1010. CHEMICAL REVIEWSa
  163285. GABRIEL WEATHERHEAD
  163286. 9992N
  163287. 2/28/96V
  163288. A REVIEW. DOWD, PAUL; IRNGARTINGER, HERMANN. TRICYCLO[2.1.0.02,5]PENTANE AND ITS DERIVATIVES. 1989, 89(5), 985 96. CHEMICAL REVIEWSa
  163289. GABRIEL WEATHERHEAD
  163290. 9993N
  163291. 2/28/96VYA REVIEW. WIBERG, KENNETH B. SMALL RING PROPELLANES. 1989, 89(5), 975 96 CHEMICAL REVIEWSa
  163292. GABRIEL WEATHERHEAD
  163293. 9994N
  163294. 2/28/96
  163295. A REVIEW. KRAKOWIAK, KRZYSZTOF E.; BRADSHAW, JERALD S.; ZAMECKA KRAKOWIAK, DARIA J. SYNTHESIS OF AZA CROWN ETHERS. 1989, 89(4), 929 72. CHEMICAL REVIEWSa
  163296. GABRIEL WEATHERHEAD
  163297. 9995N
  163298. 2/28/96V
  163299. A REVIEW. MARYANOFF BRUCE E., REITZ, ALLEN B. THE WITTIG OLEFINATION REACTION AND MODIFICATIONS INVOLVING PHOSPHORYLSTABILIZED CARBANIONS. STEREOCHEMISTRY, MECHANISM, AND SELECTED SYNTHETIC ASPECTS. 1989, 89(4), 863 927. CHEMICAL REVIEWSa
  163300. GABRIEL WEATHERHEAD
  163301. 9996N
  163302. 2/28/96V
  163303. A REVIEW. KATRITZKY, ALAN R.; DENNIS, NICHOLAS. CYCLOADDITION REACTIONS OF HETEROAROMATIC SIX MEMBERED RINGS. 1989, 89(4), 827 61. CHEMICAL REVIEWSa
  163304. GABRIEL WEATHERHEAD
  163305. 9997N
  163306. 2/28/96VnA REVIEW. CRAINE, LESLIE; RABAN, MORTON. THE CHEMISTRY OF SULFENAMIDES. 1989, 89(4), 689 712. CHEMICAL REVIEWSa
  163307. GABRIEL WEATHERHEAD
  163308. 9998N
  163309. 2/28/96
  163310. A REVIEW. SMITH, KEITH. CONTROLLED ORGANIC SYNTHESIS WITH THE AID OF MICROPOROUS SOLIDS. 1989, NO. 2, 272 8. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163311. GABRIEL WEATHERHEAD
  163312. 9999N
  163313. 2/28/96V|A REVIEW. COLLIN, JACQUELINE. DOUBLE CARBONYLATION REACTIONS. 1988, NO. 6, 976 81. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163314. GABRIEL WEATHERHEAD
  163315. 10000N
  163316. 2/28/96V
  163317. A REVIEW. KAGAN, HENRI B. ASYMMETRIC CATALYSIS IN ORGANIC SYNTHESIS WITH INDUSTRIAL PERSPECTIVES. 1988, NO. 5, 846 53. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163318. GABRIEL WEATHERHEAD
  163319. 10001N
  163320. 2/28/96V
  163321. A REVIEW. AGAMI, CLAUDE. MECHANISM OF THE PROLINE CATALYZED ENANTIOSELECTIVE ALDOL REACTION. RECENT ADVANCES. 1988, NO. 3, 499 507. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163322. GABRIEL WEATHERHEAD
  163323. 10002N
  163324. 2/28/96
  163325. A REVIEW. TONELLATO, UUMBERTO. ESTEROLYTIC REACTIVITY IN MICELLAR ASSEMBLIES AND IN CYCLODEXTRIN MACROCYCLES. 1988, NO. 2, 277 82. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163326. GABRIEL WEATHERHEAD
  163327. 10003N
  163328. 2/28/96V
  163329. A REVIEW. DE MAYER LEO C. M. CHEMICAL RELAXATION METHODS IN ORGANIC CHEMISTRY. 1988, NO. 2, 243 52. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163330. GABRIEL WEATHERHEAD
  163331. 10004N
  163332. 2/28/96V
  163333. A REVIEW. SEYDEN PENNE, JACQUELINE. LITHIUM COORDINATION BY WITTIG HORNER REAGENTS FORMED BY B CARBONYL SUBSTITUTED PHOSPHONATES AND PHOSPHINE OXIDE. 1988, NO. 2, 238 42. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  163334. GABRIEL WEATHERHEAD
  163335. 10005N
  163336. 2/28/96ViA REVIEW. SEOANE, CARLOS. TEACHING ORGANIC SYNTHESIS: WHY, HOW WHAT? 1989, 22(2), 41 6. ALDRICHIMICA ACTAa
  163337. GABRIEL WEATHERHEAD
  163338. 10006N
  163339. 2/28/96
  163340. V|A REVIEW. WISWESSER, WILLIAM J. JOHANN JOSEF LOSCHMIDT (1821 1895): A FORGOTTEN GENIUS. 1989, 22(1),17 19. ALDRICHIMICA ACTAa
  163341. GABRIEL WEATHERHEAD
  163342. 10007N
  163343. 2/28/96V
  163344. A REVIEW. SALTER, IAN D. HETERONUCLEAR CLUSTER CHEMISTRY OF COPPER SILVER, AND GOLD. 1989, 29, 249 343. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  163345. GABRIEL WEATHERHEAD
  163346. 10008N
  163347. 2/28/96V
  163348. A REVIEW. LEBOZEC HUBERT; TOUCHARD, DANIEL; DIXNEUF, PIERRE H. ORGANOMETALLIC CHEMISTRY OF ARENE RUTHENIUM AND OSMIUM COMPLEXES. 1989, 29, 163 247. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  163349. GABRIEL WEATHERHEAD
  163350. 10009N
  163351. 2/28/96V
  163352. A REVIEW. WINTER, MARK J. UNSATURATED DIMETAL CYCLOPENTADIENYL CARBONYL COMPLEXES. 1989, 29, 101 62. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  163353. GABRIEL WEATHERHEAD
  163354. 10010N
  163355. 2/28/96V
  163356. A REVIEW. TEMPLETON, JOSEPH L. FOUR ELECTRON ALKYNE LIGANDS IN MOLYBDENUM(II) AND TUNGSTEN(II) COMPLEXES. 1989, 29, ADVANCES IN ORGANOMETALLIC CHEMISTRY
  163357. GABRIEL WEATHERHEAD
  163358. 10011N
  163359. 2/28/96V
  163360. A REVIEW. TSUGE, O.; KANEMASA, S. RECENT ADVANCES IN AZOMETHINE YLIDE CHEMISTRY. 1989, 45, 231 349. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  163361. GABRIEL WEATHERHEAD
  163362. 10012N
  163363. 2/28/96V
  163364. A REVIEW. BELEN'KII, L. 1. THE LITERATURE OF HETEROCYCLIC CHEMISTRY. PART III. 1988, 44, 269 396. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  163365. GABRIEL WEATHERHEAD
  163366. 10013N
  163367. 2/28/96V
  163368. A REVIEW. COMINS, DANIEL L.; O'CONNOR, SEAN. REGIOSELECTIVE SUBSTITUTION IN AROMATIC SIX MEMBERED NITROGEN HETEROCYCLES. 1988, 44, 199 267. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  163369. GABRIEL WEATHERHEAD
  163370. 10014N
  163371. 2/28/96V
  163372. A REVIEW. ARAN, VICENTE J.; GOYA, PIIAR; OCHOA, CARMEN. HETEROCYCLES CONTAINING THE SULFAMIDE MOIETY. 1988, 44, 81 179. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  163373. GABRIEL WEATHERHEAD
  163374. 10015N
  163375. 2/28/96
  163376. A REVIEW. MCGILL, CHARLES K.; RAPPA, ANGELA. ADVANCES IN THE CHICHIBABIN REACTION. 1988 44, 1 79. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  163377. GABRIEL WEATHERHEAD
  163378. 10016N
  163379. 2/28/96V
  163380. A REVIEW. HARDING, STEPHEN E. THE MACROSTRUCTURE OF MUCUS GLYCOPROTEINS IN SOLUTION. 1989, 47, 345 381. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163381. GABRIEL WEATHERHEAD
  163382. 10017N
  163383. 2/28/96V
  163384. A REVIEW. TOMASIK, PIOTR; WIEJAK, STANISLAW; PALASINSKI, MIECZYSLAW. THE THERMAL DECOMPOSITION OF CARBOHYDRATES. PART II. THE DECOMPOSITION OF STARCH. 1989, 47, 279 343. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163385. GABRIEL WEATHERHEAD
  163386. 10018N
  163387. 2/28/96V
  163388. A REVIEW. TOMASIK, PIOTR, PALASINSKI, MIECZYSLAW, WIEJAK, STANISLAW. THE THERMAL DECOMPOSITION OF CARBOHYDRATES. PART 1. THE DECOMPOSITION OF MONO , DI , AND OLIGOSACCHARIDES. 1989 47, 203 278. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163389. GABRIEL WEATHERHEAD
  163390. 10019
  163391. 2/28/96V
  163392. A REVIEW. KNIREL, YURIY A.; VINOGRADOV, EVGENY V.; MORT, ANDREW J. APPLICATION OF ANHYDROUS HYDROGEN FIUORIDE FOR THE STRUCTURAL ANALYSIS OF POLYSACCHARIDES. 1989, 47,167 202. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163393. GABRIEL WEATHERHEAD
  163394. 10020N
  163395. 2/28/96V
  163396. A REVIEW. DILL, KILIAN; CARTER, R. DOUGLAS. CARBON 13 NUCLEAR MAGNETIC RESONANCE SPECTRAL STUDIES OF THE INTERACTION OF METAL IONS WITH CARBOHYDRATES: USE OF RELAXATION PROBES. 1989, 47, 125 166. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163397. GABRIEL WEATHERHEAD
  163398. 10021N
  163399. 2/28/96V
  163400. A REVIEW. TVAROSKA, IGOR; BLEHA, TOMAS. ANOMERIC AND EXO ANOMERIC EFFECTS IN CARBOHYDRATE CHEMISTRY. 1989, 47, 45 123. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163401. GABRIEL WEATHERHEAD
  163402. 10022N
  163403. 2/28/96V
  163404. A REVIEW. ANGYAL, STEPHEN J. COMPIEXES OF METAL CATIONS WITH CARBOHYDRATES IN SOLUTION. 1989, 47,1 43. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY
  163405. GABRIEL WEATHERHEAD
  163406. 10023N
  163407. 2/28/96V
  163408. A REVIEW. THEANDER, OLOF, NELSON, DAVID A. AQUEOUS, HIGH TEMPERATURE TRANSFORMATION OF CARBOHYDRATES RELATIVE TO UTILIZATION OF BIOMASS. 1988, 46 273 329. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163409. GABRIEL WEATHERHEAD
  163410. 10024N
  163411. 2/28/96V
  163412. A REVIEW. BIERMANN, CHRISTOPHER J. HYDROLYSIS AND OTHER CLEAVAGES OF GLYCOSIDIC LINKAGES IN POLYSACCHARIDES. 1988, 46, 251 271. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163413. GABRIEL WEATHERHEAD
  163414. 10025N
  163415. 2/28/96V
  163416. A REVIEW. CLARKE, RONALD J., COATES, JOHN H., LINCOLN, STEPHEN H. INCLUSION COMPLEXES OF THE CYCLOMALTO OLIGOSACCHARIDES (CYCLODEXTRINS). 1988, 46, 205 249. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163417. GABRIEL WEATHERHEAD
  163418. 10026N
  163419. 2/28/96
  163420. A REVIEW. ZEHAVI, URI. APPLICATIONS OF PHOTOSENSITIVE PROTECTING GROUPS IN CARBOHYDRATE CHEMISTRY. 1988, 46,179 204. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163421. GABRIEL WEATHERHEAD
  163422. 10027N
  163423. 2/28/96V
  163424. A REVIEW. CSUK, RENE; GLANZER, BRIGITTE I. N.M.R. SPECTROSCOPY OF FLUORINATED MONOSACCHARIDES. 1988, 46, 73 177. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163425. GABRIEL WEATHERHEAD
  163426. 10028N
  163427. 2/28/96V
  163428. A REVIEW. HICKS, KEVIN B. HIGH PERFORMANCE LIQUID CHROMATOGRAPHY OF CARBOHYDRATES. 1988, 46, 17 72. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  163429. GABRIEL WEATHERHEAD
  163430. 10029N
  163431. 2/28/96VeA REVIEW. STOCK, LEON. COAL PYROLYSIS. 1989, 22(11), 427 433. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163432. GABRIEL WEATHERHEAD
  163433. 10030N
  163434. 2/28/96V
  163435. A REVIEW. WILLIAMS, ANDREW. CONCERTED MECHANISMS OF ACYL GROUP TRANSFER REACTIONS IN SOLUTION. 1989, 22(11), 387 92. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  163436. GABRIEL WEATHERHEAD
  163437. 10031N
  163438. 2/28/96V
  163439. A REVIEW. JUARISTI, EUSEBIO. CONFORMATIONAL ANALYSIS OF SIX MEMBERED, SULFUR CONTAINING SATURATED HETEROCYCLES. 1989 22(10), 357 64. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163440. GABRIEL WEATHERHEAD
  163441. 10032N
  163442. 2/28/96V
  163443. A REVIEW. GUTHRIE, ROBERT D.; JENCKS, WILIAM P. IUPAC RECOMMENDATIONS FOR THE REPRESENTATION OF REACTION MECHANISMS. 1989, 22(10), 343 49. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163444. GABRIEL WEATHERHEAD
  163445. 10033N
  163446. 2/28/96V
  163447. A REVIEW. ARMENTROUT, P. B.; BEAUCHAMP, J. L. THE CHEMISTRY OF ATOMIC TRANSITION METAL IONS: INSIGHT INTO FUNDAMENTAL ASPECTS OF ORGANOMETALLIC CHEMISTRY. 1989, 22(9), 315 21. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163448. GABRIEL WEATHERHEAD
  163449. 10034N
  163450. 2/28/96V
  163451. A REVIEW. SCHWARZ, HELMUT. REMOTE FUNCTIONALIZATION OF C H AND C C BONDS BY NAKED TRANSITION METAL IONS (COSI FAN TUTTE). 1989, 22(8), 282 7. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCH
  163452. GABRIEL WEATHERHEAD
  163453. 10035N
  163454. 2/28/96V
  163455. A REVIEW. BIEHL, EDWARD R.; KHANAPURE, SUBHASH P. SYNTHESIS OF POLYCYCLICS VIA ARYNE ARYLATION REACTIONS. 1989, 22(8), 275 81 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163456. GABRIEL WEATHERHEAD
  163457. 10036N
  163458. 2/28/96V
  163459. A REVIEW. PERRIN, CHARLES L. PROTON EXCHANGE IN AMIDES: SURPRISES FROM SIMPLE SYSTEMS. 1989, 22(8), 268 75. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  163460. GABRIEL WEATHERHEAD
  163461. 10037N
  163462. 2/28/96V{A REVIEW. YOSHIDA, Z., SHIBA, T.; OHSHIRO, Y.; EDS. NEW ASPECTS OF ORGANIC CHEMISTRY, 1. KODANSHA LTD.: TOKYO, JAPAN, 1990.a
  163463. GABRIEL WEATHERHEAD
  163464. 10038N
  163465. 2/28/96V
  163466. A REVIEW. WEBER, E.; TONER, J. L.; GOLDBERG, 1.; VOEGTLE, F.; LAIDLER, D. A. STODDART, J. F., BARTSCH, R. A., ET AL. CROWN ETHERS AND ANALOGS. WILEY: CHICHESTER, U.K., 1989.a
  163467. GABRIEL WEATHERHEAD
  163468. 10039N
  163469. 2/28/96
  163470. VYA REVIEW. SCHEFFOLD, R. E. MODERN SYNTHETIC METHODS, VOL. 5. SPRINGER: BERLIN, FRG, 1989.a
  163471. GABRIEL WEATHERHEAD
  163472. 10040N
  163473. 2/28/96VfA REVIEW. SCAIANO, J. C., ED. CRC HANDBOOK OF ORGANIC PHOTOCHEMISTRY. CRC PRESS: BOCA RATON, FL, 1989.a
  163474. GABRIEL WEATHERHEAD
  163475. 10041N
  163476. 2/28/96V
  163477. A REVIEW. RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 5: STRUCTURE ELUCIDATION, PART B. ELSEVIER: AMSTERDAM, 1989.a
  163478. GABRIEL WEATHERHEAD
  163479. 10042N
  163480. 2/28/96ViA REVIEW. NEFEDOV, 0. M. CHEMISTRY OF CARBENES AND SMALL SIZED CYCLIC COMPOUNDS. MIR: MOSCOW, USSR, 1989.a
  163481. GABRIEL WEATHERHEAD
  163482. 10043N
  163483. 2/28/96VkA REVIEW. JURCZAK, J., BARANOWSKI B., EDITORS. HIGH PRESSURE CHEMICAL SYNTHESIS. ELSEVIER: AMSTERDAM, 1989.a
  163484. GABRIEL WEATHERHEAD
  163485. 10044N
  163486. 2/28/96VXA REVIEW. GUTSCHE, C. D. CALIXARENES. ROYAL SOCIETY OF CHEMISTRY: CAMBRIDGE, U.K., 1989.a
  163487. GABRIEL WEATHERHEAD
  163488. 10045
  163489. 2/28/96V[A REVIEW. FRY, ALBERT J. SYNTHETIC ORGANIC ELECTROCHEMISTRY, 2ND ED. WILEY: NEW YORK, 1989.a
  163490. GABRIEL WEATHERHEAD
  163491. 10046N
  163492. 2/28/96VpA REVIEW. FALK, HEINZ. THE CHEMISTRY OF LINEAR OLIGOPYRROLES AND BILE PIGMENTS. SPRINGER: VIENNA, AUSTRIA, 1989.a
  163493. GABRIEL WEATHERHEAD
  163494. 10047N
  163495. 2/28/96VjA REVIEW. ELSCHENBROICH, C.; SALZER, A. ORGANOMETALLICS. A CONCISE INTRODUCTION. VCH: WEINHEIM, FRG, 1989.a
  163496. GABRIEL WEATHERHEAD
  163497. 10048N
  163498. 2/28/96VQA REVIEW. EGE, S. N. ORGANIC CHEMISTRY, 2ND ED. D. C. HEATH: LEXINGTON, MA, 1989.a
  163499. GABRIEL WEATHERHEAD
  163500. 10049N
  163501. 2/28/96V}A REVIEW. DUNN A. D., RUDORF, W. D., EDS. CARBON DISULPHIDE IN ORGANIC CHEMISTRY. ELLIS HORWOOD LTD.: CHICHESTER, U.K., 1989.a
  163502. GABRIEL WEATHERHEAD
  163503. 10050N
  163504. 2/28/96VmA REVIEW. DEV, SUKH, ED. CRC HANDBOOK OF TERPENOIDS. TRITERPENOIDS, VOL. II. CRC PRESS: BOCA RATON, FL, 1989.a
  163505. GABRIEL WEATHERHEAD
  163506. 10051N
  163507. 2/28/96VlA REVIEW. DEV, SUKH, ED. CRC HANDBOOK OF TERPENOIDS. TRITERPENOIDS, VOL. 1. CRC PRESS: BOCA RATON, FL, 1989.a
  163508. GABRIEL WEATHERHEAD
  163509. 10052N
  163510. 2/28/96V
  163511. A REVIEW. WENDER, PAUL A.; SIGGEL, LORENZ; NUSS, JOHN M. ARENE ALKENE PHOTOCYCLOADDITION REACTIONS. ORGANIC PHOTOCHEMISTRY. VOLUME 10, ALBERT PADWA, ED., DEKKER: NEW YORK, 1989.a
  163512. GABRIEL WEATHERHEAD
  163513. 10053N
  163514. 2/28/96V
  163515. A REVIEW. SCAIANO, J. C.; JOHNSTON, L. J. PHOTOCHEMISTRY OF REACTION INTERMEDIATES. ORGANIC PHOTOCHEMISTRY. VOLUME 10, ALBERT PADWA, ED., DEKKER: NEW YORK, 1989.a
  163516. GABRIEL WEATHERHEAD
  163517. 10054N
  163518. 2/28/96V
  163519. A REVIEW. LAARHOVEN, WIM H. PHOTOCYCLIZATIONS AND INTRAMOLECULAR PHOTOCYCLOADDITIONS OF CONJUGATED ARYLOLEFINS AND RELATED COMPOUNDS. ORGANIC PHOTOCHEMISTRY. VOLUME 10, ALBERT PADWA, ED., DEKKER: NEW YORK, 1989.a
  163520. GABRIEL WEATHERHEAD
  163521. 10055N
  163522. 2/28/96
  163523. A REVIEW. BECKER, DAN; HADDAD, NIZAR. APPLICATIONS OF INTRAMOLECULAR 2 + 2 PHOTOCYCLOADDITIONS IN ORGANIC SYNTHESIS. ORGANIC PHOTOCHEMISTRY. VOLUME 10, ALBERT PADWA, ED., DEKKER: NEW YORK, 1989.a
  163524. GABRIEL WEATHERHEAD
  163525. 10056N
  163526. 2/28/96V
  163527. A REVIEW. MARKOVSKII, L. N.; PASHINNIK, V. E. FLUORINATION OF ORGANIC COMPOUNDS WITH FLUOROSULFURANES. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163528. GABRIEL WEATHERHEAD
  163529. 10057N
  163530. 2/28/96V
  163531. A REVIEW. BURMAKOV, A. I.; KUNSHENKO, B. V.; ALEKSEEVA, L. A.; YAGUPOLSKII, L. M. NEW USES OF SULFUR TETRAFLUORIDE IN ORGANIC SYNTHESIS. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163532. GABRIEL WEATHERHEAD
  163533. 10058N
  163534. 2/28/96
  163535. A REVIEW. BOGULAVSKAYA, L. S.; CHUVATKIN, N. N. HALOGEN FLUORIDES IN ORGANIC SYNTHESIS. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163536. GABRIEL WEATHERHEAD
  163537. 10059N
  163538. 2/28/96V
  163539. A REVIEW. FURIN, G. G.; BARDIN, V. V. HIGHER FLUORIDES OF GROUP V AND VI ELEMENTS AS FLUORINATING AGENTS IN ORGANIC SYNTHESIS. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163540. GABRIEL WEATHERHEAD
  163541. 10060N
  163542. 2/28/96V
  163543. A REVIEW. MAKHAMETSIN, F. M. HYPOFLUORITES AND THEIR APPLICATION IN ORGANIC SYNTHESIS. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163544. GABRIEL WEATHERHEAD
  163545. 10061N
  163546. 2/28/96V
  163547. A REVIEW. FURIN, G. G. SOME ELECTROPHILIC FLUORINATION AGENTS. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.
  163548. GABRIEL WEATHERHEAD
  163549. 10062N
  163550. 2/28/96V
  163551. A REVIEW. BARDIN, V. V.; YAGUPOLSKII, YU. L. XENON DIFLUORIDE. NEW FLUORINNTING AGENTS IN ORGANIC SYNTHESIS, L. GERMAN AND S. ZEMSKOV, EDS., SPRINGER VERLAG: BERLIN, 1989.a
  163552. GABRIEL WEATHERHEAD
  163553. 10063N
  163554. 2/28/96V
  163555. A REVIEW. OJIMA, IWAO; CLOS, NURIA; BASTOS, CECLIA. RECENT ADVANCES IN CATALYTIC ASYMMETRIC REACTIONS PROMOTED BY TRANSITION METAL COMPLEXES. 1989, 45(22), 6901 39. TETRAHEDRONa
  163556. GABRIEL WEATHERHEAD
  163557. 10064N
  163558. 2/28/96V
  163559. A REVIEW. KABALKA, GEORGE W.; VARMA, RAJENDER S. THE SYNTHESIS OF RADIOLABELED COMPOUNDS VIA ORGANOMETALLIC INTERMEDIATES. 1989, 45(21), 6601 21. TETRAHEDRONa
  163560. GABRIEL WEATHERHEAD
  163561. 10065N
  163562. 2/28/96V~A REVIEW. BASCHANG, G. MURAMYL PEPTIDES AND LIPOPEPTIDES: STUDIES TOWARDS IMMUNOSTIMULANTS. 1989, 45(20), 6331 60. TETRAHEDRONa
  163563. GABRIEL WEATHERHEAD
  163564. 10066N
  163565. 2/28/96
  163566. VsA REVIEW. MARKOVSKII, L. N., ROMANENKO, V. D. PHOSPHAALKYNES AND PHOSPHAALKENES. 1989, 45(19), 6019 90. TETRAHEDRONa
  163567. GABRIEL WEATHERHEAD
  163568. 10067N
  163569. 2/28/96V
  163570. A REVIEW. DAVIS, FRANKLIN A., SHEPPARD, AURELIA C. APPLICATIONS OF OXAZIRIDINES IN ORGANIC SYNTHESIS. 1989, 45(18), 5703 42. TETRAHEDRONa
  163571. GABRIEL WEATHERHEAD
  163572. 10068N
  163573. 2/28/96V
  163574. A REVIEW. TOONE, ERIC J.; SIMON, ETHAN S.; BEDNARSKI, MARK D.; WHITESIDES, GEORGE M. ENZYME CATALYZED SYNTHESIS OF CARBOHYDRATES. 1989, 45(17), 5365 422. TETRAHEDRONa
  163575. GABRIEL WEATHERHEAD
  163576. 10069N
  163577. 2/28/96V~A REVIEW. BAULD, NATHAN L. CATION RADICAL CYCLOADDITIONS AND RELATED SIGMATROPIC REACTIONS. 1989, 45(17), 5307 63. TETRAHEDRONa
  163578. GABRIEL WEATHERHEAD
  163579. 10070N
  163580. 2/28/96V
  163581. A REVIEW. POLLACK, RALPH M. STEREOELECTRONIC CONTROL IN THE REACTIONS OF KETONES AND THEIR ENOL(ATE)S. 1989, 45(16), 4913 38. TETRAHEDRONa
  163582. GABRIEL WEATHERHEAD
  163583. 10071N
  163584. 2/28/96
  163585. A REVIEW. MCDONALD, RICHARD N. GENERATION, THERMOCHEMISTRY AND CHEMISTRY OF CARBENE ANION RADICALS AND RELATED SPECIES. 1989, 45(13), 3993 4015. TETRAHEDRONa
  163586. GABRIEL WEATHERHEAD
  163587. 10072N
  163588. 2/28/96V
  163589. A REVIEW. WOZNIAK, L., CHOJNOWSKI, J. SILYL ESTERS OF PHOSPHORUS
  163590. COMMON INTERMEDIATES IN SYNTHESIS. 1989, 45(9), 2465 524. TETRAHEDRONa
  163591. GABRIEL WEATHERHEAD
  163592. 10073N
  163593. 2/28/96VgA REVIEW. SERVI, STEFANO. BAKERS' YEAST AS A REAGENT IN ORGANIC SYNTHESIS. 1990, NO. 1, 1 25. SYNTHESISa
  163594. GABRIEL WEATHERHEAD
  163595. 10074N
  163596. 2/28/96V
  163597. A REVIEW. LENOIR, DIETER. THE APPLICATION OF LOW VALENT TITANIUM REAGENTS IN ORGANIC SYNTHESIS. 1989, NO. 12, 883 97. SYNTHESISa
  163598. GABRIEL WEATHERHEAD
  163599. 10075N
  163600. 2/28/96V
  163601. A REVIEW. EINHORN, CATHY; EINHORN, JACQUES; LUCHE, JEAN LOUIS. SONOCHEMISTRY
  163602. THE USE OF ULTRASONIC WAVES IN SYNTHETIC ORGANIC CHEMISTRY. 1989, NO. 11, 787 813. SYNTHESISa
  163603. GABRIEL WEATHERHEAD
  163604. 10076
  163605. 2/28/96V
  163606. A REVIEW. RICCI, ALFREDO; DEGL'INNOCENTI, ALESSANDRO. SYNTHESIS AND SYNTHETIC POTENTIAL OF ACYLSILANES. 1989, NO. 9, 647 60. SYNTHESISa
  163607. GABRIEL WEATHERHEAD
  163608. 10077N
  163609. 2/28/96V
  163610. A REVIEW. NOVOTNY, MILOS V. RECENT DEVELOPMENTS IN ANALYTICAL CHROMATOGRAPHY. 1989, 246(4926), 51 57. SCIENCE (WASHINGTON, D.C. 1883 )a
  163611. GABRIEL WEATHERHEAD
  163612. 10078N
  163613. 2/28/96VyA REVIEW. WONG C. H. ENZYMIC CATALYSTS IN ORGANIC SYNTHESIS. 1989, 244(4909), 1145 1152. SCIENCE (WASHINGTON, D.C. 1883 )a
  163614. GABRIEL WEATHERHEAD
  163615. 10079N
  163616. 2/28/96V
  163617. A REVIEW. MCMURRY, THOMAS J.; RAYMOND, KENNETH N.; SMITH, PAUL H. MOLECULAR RECOGNITION AND METAL ION TEMPLATE SYNTHESIS. 1989, 244(4907), 938 943. SCIENCE (WASHINGTON, D.C. 1883 )a
  163618. GABRIEL WEATHERHEAD
  163619. 10080N
  163620. 2/28/96VwA REVIEW. CURL, ROBERT F., SMALLEY, RICHARD E. PROBING C60. 1988 242(4881), 1017 1022. SCIENCE (WASHINGTON, D.C. 1883 )a
  163621. GABRIEL WEATHERHEAD
  163622. 10081N
  163623. 2/28/96V
  163624. A REVIEW. ANTONOVA, A. B.; IOGANSON, A. A. TRANSITION METAL COMPLEXES OF UNSATURATED CARBENES: SYNTHESIS, STRUCTURE AND REACTIVITY. 1989, 58(7), 693 710. RUSSIAN CHEMICAL REVIEWSa
  163625. GABRIEL WEATHERHEAD
  163626. 10082N
  163627. 2/28/96VfA REVIEW. MOISEEV, I. I. CARBENE COMPLEXES IN CATALYSIS. 1989, 58(7), 682 92. RUSSIAN CHEMICAL REVIEWSa
  163628. GABRIEL WEATHERHEAD
  163629. 10083N
  163630. 2/28/96V
  163631. A REVIEW. PROTOPOPOVA, M. N., SHAPIRO, E. A. CARBENE SYNTHESIS AND CHEMICAL REACTIONS OF 3 CYCLOPROPENECARBOXYLATE ESTERS
  163632. PROMISING INTERMEDIATES FOR ORGANIC SYNTHESIS. 1989, 58(7), 667 81. RUSSIAN CHEMICAL REVIEWSa
  163633. GABRIEL WEATHERHEAD
  163634. 10084N
  163635. 2/28/96V
  163636. A REVIEW. KOSTIKOV, R. R., MOLCHANOV A. P., KHLEBNIKOV, A. F. HALOGEN CONTAINING CARBENES. 1989, 58(7), 654 66. RUSSIAN CHEMICAL REVIEWSa
  163637. GABRIEL WEATHERHEAD
  163638. 10085N
  163639. 2/28/96
  163640. A REVIEW. PETROSYAN, V. A.; NIYAZYMBETOV, M. E. ELECTROCHEMICAL METHODS FOR THE GENERATION OF CARBENES AND THEIR ANALOGS. 1989, 58(7), 644 53. RUSSIAN CHEMICAL REVIEWSa
  163641. GABRIEL WEATHERHEAD
  163642. 10086N
  163643. 2/28/96V
  163644. A REVIEW. ZUEV, P. S.; NEFEDOV, 0. M. SPECTROSCOPIC STUDY OF CARBENES IN LOW TEMPERATURE MATRIXES. 1989, 58(7), 636 43. RUSSIAN CHEMICAL REVIEWSa
  163645. GABRIEL WEATHERHEAD
  163646. 10087N
  163647. 2/28/96V
  163648. A REVIEW. MINKIN, V. 1.; SIMKIN, B. YA.; GLUKHOVTSEV, M. N. QUANTUM CHEMICAL STUDIES OF THE STRUCTURE AND REACTIVITY OF CARBENES. 1989, 58(7), 622 35. RUSSIAN CHEMICAL REVIEWSa
  163649. GABRIEL WEATHERHEAD
  163650. 10088N
  163651. 2/28/96V
  163652. A REVIEW. BOROVKOV, V. V., EVSTIGNEEVA, R. P.; STREKOVA, L. N.; FILIPPOVICH, E. I.; KHAIRUTDINOV, R. F. PORPHYRIN QUINONE COMPOUNDS AS SYNTHETIC MODELS OF THE REACTION CENTER IN PHOTOSYNTHESIS. 1989, 58(6), 602 19. RUSSIAN CHEMICAL REVIEWSa
  163653. GABRIEL WEATHERHEAD
  163654. 10089N
  163655. 2/28/96
  163656. A REVIEW. CHERNYSHEV, E. A.; KOMALENKOVA, N. G. THE THERMAL GAS PHASE SYNTHESIS OF HETEROCYCLIC COMPOUNDS WITH ONE OR SEVERAL SILICON ATOMS IN THE RING. 1989, 58(6), 559 74. RUSSIAN CHEMICAL REVIEWSa
  163657. GABRIEL WEATHERHEAD
  163658. 10090N
  163659. 2/28/96V
  163660. A REVIEW. MALETINA I. I.; ORDA, V. V.; YAGUPOL'SKII, L. M. FLUORINE CONTAINING ORGANIC DERIVATIVES OF POLYVALENT HALOGENS. 1989, 58(6), 544 58. RUSSIAN CHEMICAL REVIEWSa
  163661. GABRIEL WEATHERHEAD
  163662. 10091N
  163663. 2/28/96V
  163664. A REVIEW. YABLOKOVA, N. V.; ALEKSANDROV, YU. A. CATALYTIC DECOMPOSITION OF ORGANIC AND ORGANOELEMENTAL PEROXIDES IN THE PRESENCE OF ELECTRON DONORS AND ELECTRON ACCEPTORS. 1989, 58(6), 534 43. RUSSIAN CHEMICAL REVIEWSa
  163665. GABRIEL WEATHERHEAD
  163666. 10092N
  163667. 2/28/96V
  163668. A REVIEW. DERKACH, N. YA.; LEVCHENKO, E. S. AZA ANALOGS OF ORGANIC AND INORGANIC OXYGEN COMPOUNDS OF SELENIUM. 1989, 58(5), 507 16 RUSSIAN CHEMICAL REVIEWSa
  163669. GABRIEL WEATHERHEAD
  163670. 10093N
  163671. 2/28/96
  163672. A REVIEW. MAR'IN, V. P.; VYSHINSKAYA, L. I.; RAZUVAEV, G. A. THERMAL DECOMPOSITION AND PHOTODECOMPOSITION OF BIS(CYCLOPENTADIENYL) COMPLEXES OF TITANIUM, VANADIUM, AND THEIR ANALOGS. 1989, 58(5), 494 506. RUSSIAN CHEMICAL REVIEWSa
  163673. GABRIEL WEATHERHEAD
  163674. 10094N
  163675. 2/28/96V
  163676. A REVIEW. MARKARYAN, E. A.; SAMODUROVA, A. G. ADVANCES IN THE CHEMISTRY OF ISOCHROMAN. 1989, 58(5), 479 93. RUSSIAN CHEMICAL REVIEWSa
  163677. GABRIEL WEATHERHEAD
  163678. 10095N
  163679. 2/28/96VyA REVIEW. ZLOTIN S. G.; VARNAEVA, G. N.; LUK'YANOVA, 0. A. A NITRONITRILES. 1989, 58(5), 470 78. RUSSIAN CHEMICAL REVIEWSa
  163680. GABRIEL WEATHERHEAD
  163681. 10096N
  163682. 2/28/96V
  163683. A REVIEW. PAVLENKO, N. V. THE VAPOR PHASE HETEROGENEOUS CATALYTIC HYDROGENATION OF CARBONYL COMPOUNDS AND CARBON MONOXIDE. 1989, 58(5), 453 69.a
  163684. GABRIEL WEATHERHEAD
  163685. 10097N
  163686. 2/28/96
  163687. V~A REVIEW. GEL
  163688. MBOL'DT, V. 0. ENNAN, A. A. PENTACOORDINATE FLUOROSILICATE ANIONS. 1989, 58(4), 371 80. RUSSIAN CHEMICAL REVIEWSa
  163689. GABRIEL WEATHERHEAD
  163690. 10098N
  163691. 2/28/96V
  163692. A REVIEW. SINYASHIN, 0. G.; BATYEVA, E. S., PUDOVIK, A. N. PROGRESS IN THE CHEMISTRY OF THIO DERIVATIVES OF TRIVALENT PHOSPHORUS ACIDS. 1989, 58(4), 352 70. RUSSIAN CHEMICAL REVIEWSa
  163693. GABRIEL WEATHERHEAD
  163694. 10099N
  163695. 2/28/96V
  163696. A REVIEW. BADANYAN, SH. 0., MELIKYAN, G. G.; MKRTCHYAN, D. A. THE INTRODUCTION OF FUNCTIONAL GROUPS INTO UNSATURATED SYSTEMS BY CARBONYL COMPOUNDS IN THE PRESENCE OF MANGANESE(III) ACETATE. 1989, 58(3), 286 96. RUSSIAN CHEMICAL REVIEWSa
  163697. GABRIEL WEATHERHEAD
  163698. 10100N
  163699. 2/28/96V
  163700. A REVIEW. BURSIAN, N. R.; KOGAN, S. B. CATALYTIC CONVERSION OF PARAFFINIC HYDROCARBONS INTO ISOPARAFFINS AND OLEFINS. 1989, 58(3), 272 85. RUSSIAN CHEMICAL REVIEWSa
  163701. GABRIEL WEATHERHEAD
  163702. 10101N
  163703. 2/28/96
  163704. A REVIEW. MIRSKOVA, A. N., DROZDOVA, T. 1., LEVKOVSKAYA, G. G. VORONKOV, M. G. REACTIONS OF N CHLORAMINES AND N HALOAMIDES WITH UNSATURATED COMPOUNDS. 1989, 58(3) 250 71 . RUSSIAN CHEMICAL REVIEWSa
  163705. GABRIEL WEATHERHEAD
  163706. 10102N
  163707. 2/28/96V
  163708. A REVIEW. KISELEV, V. D.; KONOVALOV, A. I. FACTORS THAT DETERMINE THE REACTIVITY OF REACTANTS IN THE NORMAL AND CATALYZED DIELS ALDER REACTION. 1989, 58(3), 230 49. RUSSIAN CHEMICAL REVIEWSa
  163709. GABRIEL WEATHERHEAD
  163710. 10103N
  163711. 2/28/96V
  163712. A REVIEW. SHKLOVER, V. E.; STRUCHKOV, YU. T.; VORONKOV, M. G. ORGANOSILICON COMPOUNDS WITH NONSTANDARD TYPES OF COORDINATION. 1989, 58(3), 211 29. RUSSIAN CHEMICAL REVIEWSa
  163713. GABRIEL WEATHERHEAD
  163714. 10104N
  163715. 2/28/96V
  163716. A REVIEW. PASYNSKII, A. A., EREMENKO I. L. HETEROMETALLIC SULFIDE BRIDGED CLUSTERS OF TRANSITION ELEMENTS. 1989, 58(2), 181 99. RUSSIAN CHEMICAL REVIEWSa
  163717. GABRIEL WEATHERHEAD
  163718. 10105N
  163719. 2/28/96
  163720. A REVIEW. SOBENINA, L. N.; MIKHALEVA, A. I.; TROFIMOV, B. A. SYNTHESIS OF PYRROLES FROM ALIPHATIC COMPOUNDS. 1989, 58(2), 163 80. RUSSIAN CHEMICAL REVIEWSa
  163721. GABRIEL WEATHERHEAD
  163722. 10106N
  163723. 2/28/96V
  163724. A REVIEW. SHAFRAN, YU. M.; BAKULEV, V. A., MOKRUSHIN, V. S SYNTHESIS AND PROPERTIES OF A AMINO NITRILES. 1989, 58(2) RUSSIAN CHEMICAL REVIEWSa
  163725. GABRIEL WEATHERHEAD
  163726. 10107N
  163727. 2/28/96V
  163728. A REVIEW. LAPIDUS, A. L.; PIROZHKOV, S. D. CATALYTIC SYNTHESIS OF ORGANIC COMPOUNDS BY CARBONYLATION OF UNSATURATED HYDROCARBONS AND ALCOHOLS. 1989, 58(2), 117 37. RUSSIAN CHEMICAL REVIEWSa
  163729. GABRIEL WEATHERHEAD
  163730. 10108N
  163731. 2/28/96V
  163732. A REVIEW. TREGER, YU. A.; ROZANOV, V. N. THE SYNTHESIS OF ORGANOCHLORINE COMPOUNDS FROM ONE CARBON MOLECULES. 1989, 58(1), 84 99. RUSSIAN CHEMICAL REVIEWSa
  163733. GABRIEL WEATHERHEAD
  163734. 10109N
  163735. 2/28/96
  163736. A REVIEW. KORNEEVA, G. A., LOKTEEV, S. M. THE SYNTHESIS OF ETHYLENE GLYCOL FROM FORMALDEHYDE. 1989, 58(1), 73 83. RUSSIAN CHEMICAL REVIEWSa
  163737. GABRIEL WEATHERHEAD
  163738. 10110N
  163739. 2/28/96V
  163740. A REVIEW. SLIVINSKII, E. V.; VOITSEKHOVSKII, YU. P. DEVELOPMENT OF IDEAS CONCERNING THE MECHANISM OF THE FISCHER TROPSCH SYNTHESIS. 1989, 58(1), 57 72. RUSSIAN CHEMICAL REVIEWSa
  163741. GABRIEL WEATHERHEAD
  163742. 10111N
  163743. 2/28/96VuA REVIEW. ROZOVSKII, A. YA. CONTEMPORARY PROBLEMS IN METHANOL SYNTHESIS. 1989, 58(1), 41 56. RUSSIAN CHEMICAL REVIEWSa
  163744. GABRIEL WEATHERHEAD
  163745. 10112N
  163746. 2/28/96V
  163747. A REVIEW. GRYAZNOV, V. M., GUL'YANOVA, S. G., SEROV, YU. M. THE ROLE OF ADSORBED FORMS OF HYDROGEN AND OXYGEN IN TRANSFORMATIONS OF OXYGEN CONTAINING ONE CARBON MOLECULES ON MEMBRANE CATALYSTS. 1989, 58(1), 35 40. RUSSIAN CHEMICAL REVIEWSa
  163748. GABRIEL WEATHERHEAD
  163749. 10113N
  163750. 2/28/96
  163751. A REVIEW. SINEV, M. YU.; KORCHAK, V. N.; KRYLOV, 0. V. THE MECHANISM OF PARTIAL OXIDATION OF METHANE. 1989, 58(1), 22 34. RUSSIAN CHEMICAL REVIEWSa
  163752. GABRIEL WEATHERHEAD
  163753. 10114N
  163754. 2/28/96V
  163755. A REVIEW. SOKOLOVSKII, V. D., YUR'EVA, T. M., MATROS, YU. SH.; IONE K. G.; LIKHOLOBOV, V. A.; PARMON, V. N.; ZAMARAEV, K. I. CATALYTIC CHEMISTRY AND TECHNOLOGY OF ONE CARBON COMPOUNDS. 1989, 58(1), 2 21. RUSSIAN CHEMICAL REVIEWSa
  163756. GABRIEL WEATHERHEAD
  163757. 10115N
  163758. 2/28/96V
  163759. A REVIEW. VAN BEKKUM H., KOUWENHOVEN, H. W. THE USE OF ZEOLITES IN ORGANIC REACTIONS. 1989, 108(9), 283 294. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  163760. GABRIEL WEATHERHEAD
  163761. 10116N
  163762. 2/28/96V
  163763. A REVIEW. WIELSTRA, YYSEN, GAMBAROTTA, SANDRO  CHIANG, MICHAEL Y. THE ELUSIVE ZIRCONIUM(III). 1989,108(1), 1 6. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  163764. GABRIEL WEATHERHEAD
  163765. 10117N
  163766. 2/28/96
  163767. A REVIEW. BROWN, R. F. C. THERMAL REARRANGEMENTS OF ALKYNES UNDER FLASH VACUUM PYROLYSIS CONDITIONS. THE ACETYLENE METHYLENECARBENE REARRANGEMENT. 1988,107(12), 655 661. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  163768. GABRIEL WEATHERHEAD
  163769. 10118N
  163770. 2/28/96V
  163771. A REVIEW. STODDART, J. FRASER; ZARZYCKI, RYSZARD. CYCLODEXTRINS AS SECOND SPHERE LIGANDS FOR TRANSITION METAL COMPLEXES. 1988, 107(9), 515 528. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  163772. GABRIEL WEATHERHEAD
  163773. 10119N
  163774. 2/28/96V
  163775. A REVIEW. BICKELHAUPT, FRIEDRICH; DE WOLF, WILLEM H. BRIDGED VALENCE ISOMERS OF BENZENE AND CYCLOPHANES. 1988,107(7 8), 459 478. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  163776. GABRIEL WEATHERHEAD
  163777. 10120N
  163778. 2/28/96V{A REVIEW. ENGELHARDT, HEINZ. CHROMATOGRAPHIC CHARACTERIZATION OF SURFACES. 1989, 61(11), 2033 6. PURE AND APPLIED CHEMISTRYa
  163779. GABRIEL WEATHERHEAD
  163780. 10121N
  163781. 2/28/96
  163782. A REVIEW. YASHIN, YA I. CHROMATOGRAPHIC RETENTION PARAMETERS AND MOLECULAR STRUCTURE. 1989, 61(11), 2021 6. PURE AND APPLIED CHEMISTRYa
  163783. GABRIEL WEATHERHEAD
  163784. 10122N
  163785. 2/28/96V
  163786. A REVIEW. KADISH, KARL M.; MU, XIHAI; ANDERSON, JAMES E. RECOMMENDED METHODS FOR THE PURIFICATION OF SOLVENTS AND TESTS FOR IMPURITIES. BENZENE AND TOLUENE. 1989, 61(10), 1823 8. PURE AND APPLIED CHEMISTRYa
  163787. GABRIEL WEATHERHEAD
  163788. 10123N
  163789. 2/28/96V
  163790. A REVIEW. VAHRENKAMP, HEINRICH. NEW INTERCONVERSIONS IN THE LIGAND SPHERE OF CLUSTERS. 1989, 61(10),1777 82. PURE AND APPLIED CHEMISTRY . A REVIEWa
  163791. GABRIEL WEATHERHEAD
  163792. 10124N
  163793. 2/28/96V~A REVIEW. DIXNEUF, PIERRE H. ACTIVATION OF ALKYNES WITH RUTHENIUM COMPLEXES. 1989, 61(10), 1763 70. PURE AND APPLIED CHEMISTRYa
  163794. GABRIEL WEATHERHEAD
  163795. 10125N
  163796. 2/28/96VpA REVIEW. KEINAN, EHUD. SILICON HYDRIDES IN ORGANIC SYNTHESIS. 1989, 61(10), 1737 46. PURE AND APPLIED CHEMISTRYa
  163797. GABRIEL WEATHERHEAD
  163798. 10126N
  163799. 2/28/96VvA REVIEW. JUTZI, PETER. MAIN GROUP METALLOCENES: RECENT DEVELOPMENTS. 1989, 61(10), 1731 6. PURE AND APPLIED CHEMISTRYa
  163800. GABRIEL WEATHERHEAD
  163801. 10127N
  163802. 2/28/96V
  163803. A REVIEW. GEOFFROY, GREGORY L.; SHERIDAN, JOHN B.; BASSNER, SHERRI L.; KELLEY, COLLEEN. MIGRATORY INSERTION OF CARBON MONOXIDE INTO METAL ACYL BONDS. 1989, 61(10),1723 9. PURE AND APPLIED CHEMISTRYa
  163804. GABRIEL WEATHERHEAD
  163805. 10128N
  163806. 2/28/96V
  163807. A REVIEW. ERKER, GERHARD. SOME NOVEL STRUCTURAL AND CHEMICAL ASPECTS OF CP SUBSTITUTED BENT METALLOCENE COMPLEXES. 1989, 61(10), 1715 22. PURE AND APPLIED CHEMISTRYa
  163808. GABRIEL WEATHERHEAD
  163809. 10129N
  163810. 2/28/96V
  163811. A REVIEW. CHISHOLM MALCOLM H. CARBON CARBON AND CARBON HYDROGEN BOND ACTIVATION AT DITUNGSTEN CENTERS SUPPORTED BY ALKOXIDE LIGANDS. 1989, 61(10),1707 14. PURE AND APPLIED CHEMISTRYa
  163812. GABRIEL WEATHERHEAD
  163813. 10130N
  163814. 2/28/96
  163815. A REVIEW. CARMONA, ERNESTO; CAMPORA, JUAN; MUNOZ, MIGUEL A.; PANEQUE, MARGARITA; POVEDA, MANUEL L. ELECTRON RICH METAL COMPLEXES FOR CARBON DIOXIDE AND CARBON DISULFIDE INCORPORATION. 1989, 61(10), 1701 6. PURE AND APPLIED CHEMISTRYa
  163816. GABRIEL WEATHERHEAD
  163817. 10131N
  163818. 2/28/96V
  163819. A REVIEW. BENNETT, MARTIN A. THE STABILIZATION AND REACTIVITY OF STRAINED CYCLIC ALKYNES ON TRANSITION METAL CENTERS. 1989, 61(10), 1695 700. PURE AND APPLIED CHEMISTRYa
  163820. GABRIEL WEATHERHEAD
  163821. 10132N
  163822. 2/28/96V
  163823. A REVIEW. VAN KOTEN, GERARD. TUNING THE REACTIVITY OF METALS HELD IN A RIGID LIGAND ENVIRONMENT. 1989, 61(10),1681 94. PURE AND APPLIED CHEMISTRYa
  163824. GABRIEL WEATHERHEAD
  163825. 10133N
  163826. 2/28/96
  163827. A REVIEW. MARKS, TOBIN J., GAGNE, MICHEL R., NOLAN, STEVEN P. SCHOCK, LAUREL E.; SEYAM, AFIF M.; STERN, DAVID. WHAT CAN METAL LIGAND BONDING ENERGETICS TEACH US ABOUT STOICHIOMETRIC AND CATALYTIC ORGANOMETAUIC CHEMISTRY? 1989, 61(10), 1665 72. PURE AND APPLIED CHEMISTRY
  163828. GABRIEL WEATHERHEAD
  163829. 10134N
  163830. 2/28/96V
  163831. A REVIEW. REBEK, JULIUS, JR. MODEL STUDIES IN RECOGNITION USING NEW MOLECULAR SHAPES. 1989, 61(9),1517 22. PURE AND APPLIED CHEMISTRYa
  163832. GABRIEL WEATHERHEAD
  163833. 10135N
  163834. 2/28/96V
  163835. A REVIEW. SCHMIDT, RICHARD R. RECENT DEVELOPMENTS IN THE SYNTHESIS OF GLYCOCONJUGATES. 1989, 61(7),1257 70. PURE AND APPLIED CHEMISTRYa
  163836. GABRIEL WEATHERHEAD
  163837. 10136N
  163838. 2/28/96
  163839. A REVIEW. FRASER REID, BERT; MOOTOO, D.; RANDY  KONRADSSON, PETER UDODONG, UKO E.; ANDREWS, C. WEBB; RATCLIFFE, ANDREW J.; WU, ZUFAN, YU, KOU LONG. NOVEL CARBOHYDRATE TRANSFORMATIONS DISCOVERED EN ROUTE TO NATURAL PRODUCTS. 1989, 61(7), 1243 56. PURE AND APPLIED CHEMISTRY
  163840. GABRIEL WEATHERHEAD
  163841. 10137N
  163842. 2/28/96V
  163843. A REVIEW. MYLES, DAVID C.; DANISHEFSKY, SAMUEL J. THE SYNTHESIS OF POLYOXYGENATED NATURAL PRODUCTS VIA FULLY SYNTHETIC BRANCHED PYRANOSE DERIVATIVES: APPLICATION TO THE ERYTHRONOLIDE PROBLEM. 1989, 61(7),1235 42. PURE AND APPLIED CHEMISTRYa
  163844. GABRIEL WEATHERHEAD
  163845. 10138N
  163846. 2/28/96V
  163847. A REVIEW. BAER, HANS H. RECENT SYNTHETIC STUDIES IN NITROGEN CONTAINING AND DEOXYGENATED SUGARS. 1989, 61(7),1217 34. PURE AND APPLIED CHEMISTRYa
  163848. GABRIEL WEATHERHEAD
  163849. 10139N
  163850. 2/28/96
  163851. A REVIEW. TVAROSKA, IGOR. COMPUTATIONAL METHODS FOR STUDYING OLIGO  AND POLYSACCHARIDE CONFORMATIONS. 1989, 61(7) 1201 16. PURE AND APPLIED CHEMISTRYa
  163852. GABRIEL WEATHERHEAD
  163853. 10140N
  163854. 2/28/96V
  163855. A REVIEW. WESTMORELAND, DAVID G., RHODES, GERALD R. ANALYTICAL TECHNIQUES FOR TRACE ORGANIC COMPOUNDS. II. DETECTORS FOR GAS CHROMATOGRAPHY. 1989, 61(6),1147 60. PURE AND APPLIED CHEMISTRYa
  163856. GABRIEL WEATHERHEAD
  163857. 10141N
  163858. 2/28/96V
  163859. A REVIEW. MEYERSTEIN, DAN. FACTORS AFFECTING THE EQUILIBRIUM CONSTANT OF HOMOLYSIS OF COMPLEXES WITH METAL CARBON S BONDS IN AQUEOUS SOLUTIONS. PULSE RADIOLYSIS STUDIES 1989, 61(5), 885 9. PURE AND APPLIED CHEMISTRYa
  163860. GABRIEL WEATHERHEAD
  163861. 10142N
  163862. 2/28/96V
  163863. A REVIEW. KIMURA, EIICHI. DEVELOPMENTS IN FUNCTIONALIZATION OF MACROCYCLIC POLYAMINES. 1989, 61(5), 823 8. PURE AND APPLIED CHEMISTRYa
  163864. GABRIEL WEATHERHEAD
  163865. 10143N
  163866. 2/28/96
  163867. A REVIEW. GRILLER, DAVID; WAYNER, DANIAL D. M. RADICAL THERMOCHEMISTRY AND ORGANIC REACTIONS. 1989, 61(4), 717 24. PURE AND APPLIED CHEMISTRYa
  163868. GABRIEL WEATHERHEAD
  163869. 10144N
  163870. 2/28/96V
  163871. A REVIEW. SCHWARZ, HELMUT. GENERATION OF ELUSIVE NEUTRALS AND DICATIONS BY NEUTRALIZATION RESP. CHARGE STRIPPING OF MONOCATIONS IN BEAM EXPERIMENTS. 1989, 61(4), 685 92 PURE AND APPLIED CHEMISTRYa
  163872. GABRIEL WEATHERHEAD
  163873. 10145N
  163874. 2/28/96V
  163875. A REVIEW. HARGITTAI, ISTVAN. VARIATIONS OF MOLECULAR GEOMETRY FROM ELECTRON DIFFRACTION. 1989, 61(4), 651 60. PURE AND APPLIED CHEMISTRYa
  163876. GABRIEL WEATHERHEAD
  163877. 10146N
  163878. 2/28/96V
  163879. A REVIEW. HOUK, K. N. AB INITIO AND EMPIRICAL COMPUTATIONS OF MECHANISM AND STEREOSELECTIVITY. 1989 61(4), 643 50. PURE AND APPLIED CHEMISTRYa
  163880. GABRIEL WEATHERHEAD
  163881. 10147N
  163882. 2/28/96
  163883. A REVIEW. HUISGEN, ROLF. KINETICS AND REACTION MECHANISMS: SELECTED EXAMPLES FROM THE EXPERIENCE OF FORTY YEARS. 1989, 61(4), 613 28. PURE AND APPLIED CHEMISTRYa
  163884. GABRIEL WEATHERHEAD
  163885. 10148N
  163886. 2/28/96V
  163887. A REVIEW. OSAWA, EIJI; GOTO, HITOSHI; OISHI, TAKESHI; OHTSUKA, YASUO; CHUMAN, TATSUJI. APPLICATION OF MOLECULAR MECHANICS TO NATURAL PRODUCT CHEMISTRY. 1989, 61(3), 597 600. PURE AND APPLIED CHEMISTRYa
  163888. GABRIEL WEATHERHEAD
  163889. 10149N
  163890. 2/28/96VzA REVIEW. OHNO, MASAJI. FROM NATURAL BLEOMYCINS TO MAN DESIGNED BLEOMYCINS. 1989, 61(3), 581 4. PURE AND APPLIED CHEMISTRYa
  163891. GABRIEL WEATHERHEAD
  163892. 10150N
  163893. 2/28/96V
  163894. A REVIEW. NORIN, TORBJOERN. SYNTHETIC AND CHEMICAL STUDIES ON PHEROMONES OF SOME FOREST PEST INSECTS. 1989, 61(3), 547 50. PURE AND APPLIED CHEMISTRYa
  163895. GABRIEL WEATHERHEAD
  163896. 10151N
  163897. 2/28/96
  163898. A REVIEW. MORI, KENJI; WATANABE, HIDENORI. RECENT RESULTS IN THE SYNTHESIS OF SEMIOCHEMICALS: SYNTHESIS OF GLYCINOECLEPIN A. 1989, 61(3) 543 6. PURE AND APPLIED CHEMISTRYa
  163899. GABRIEL WEATHERHEAD
  163900. 10152N
  163901. 2/28/96V
  163902. A REVIEW. KASHMAN, Y., CARMELY, S., BLASBERGER, D. HIRSCH, S. GREEN, D. MARINE NATURAL PRODUCTS: NEW RESULTS FROM RED SEA INVERTEBRATES. 1989, 61(3), 517 20. PURE AND APPLIED CHEMISTRYa
  163903. GABRIEL WEATHERHEAD
  163904. 10153N
  163905. 2/28/96V
  163906. A REVIEW. BRAEKMAN, J. C.; DALOZE, D.; MOUSSIAUX, B.; STOLLER, C.; DENEUBOURG, F. SPONGE SECONDARY METABOLITES: NEW RESULTS. 1989, 61(3), 509 12. PURE AND APPLIED CHEMISTRYa
  163907. GABRIEL WEATHERHEAD
  163908. 10154N
  163909. 2/28/96V
  163910. A REVIEW. OGURA, KYOZO. ARTIFICIALLY ELICITED CAPABILITIES OF ENZYMES AND THEIR APPLICATION IN NATURAL PRODUCT CHEMISTRY. 1989, 61(3), 477 80. PURE AND APPLIED CHEMISTRYa
  163911. GABRIEL WEATHERHEAD
  163912. 10155N
  163913. 2/28/96
  163914. /ViA REVIEW. ZHOU, WEISHAN. THE SYNTHESIS OF BRASSINOSTEROID. 1989, 61(3), 431 4. PURE AND APPLIED CHEMISTRYa
  163915. GABRIEL WEATHERHEAD
  163916. 10156N
  163917. 2/28/96V
  163918. A REVIEW. YAMAMOTO, HISASHI; MARUOKA, KEIJI; FURUTA, KYOJI; NARUSE, YUJI. NEW APPROACH FOR NATURAL PRODUCT SYNTHESIS USING MAIN GROUP ORGANOMETALLIC REAGENTS. 1989, 61(3), 419 22. PURE AND APPLIED CHEMISTRYa
  163919. GABRIEL WEATHERHEAD
  163920. 10157N
  163921. 2/28/96V
  163922. A REVIEW. MANDER, LEWIS N. SYNTHETIC STUDIES ON GIBBERELLINS AND ANTHERIDIOGENS. 1989, 61(3), 397 400. PURE AND APPLIED CHEMISTRYa
  163923. GABRIEL WEATHERHEAD
  163924. 10158N
  163925. 2/28/96V
  163926. A REVIEW. MATSUDA, FUYUHIKO; KAWASAKI, MOTOJI; TERASHIMA, SHIRO. SYNTHETIC STUDIES ON NOGALAMYCIN CONGENERS. TOTAL SYNTHESES OF (+) NOGARENE, (+) 7 CON 0 METHYLNOGAROL, AND THEIR RELATED COMPOUNDS. 1989, 61(3), 385 8. PURE AND APPLIED CHEMISTRYa
  163927. GABRIEL WEATHERHEAD
  163928. 10159N
  163929. 2/28/96
  163930. 3V}A REVIEW. DEV, SUKH. GUGGULTETROLS: A NEW CLASS OF NATURALLY OCCURRING LIPIDS. 1989, 61(3), 353 6. PURE AND APPLIED CHEMISTRYa
  163931. GABRIEL WEATHERHEAD
  163932. 10160N
  163933. 2/28/96V
  163934. A REVIEW. NAGATA, WATARU. CONTRIBUTIONS TO THE CHEMISTRY OF B LACTAM ANTIBIOTICS: L OXA NUCLEAR ANALOGS OF NATURALLY OCCURRING B LACTAM ANTIBIOTICS. 1989, 61(3), 325 36. PURE AND APPLIED CHEMISTRYa
  163935. GABRIEL WEATHERHEAD
  163936. 10161N
  163937. 2/28/96VpA REVIEW. KISHI, YOSHITO. NATURAL PRODUCTS SYNTHESIS: PALYTOXIN. 1989, 61(3), 313 24. PURE AND APPLIED CHEMISTRYa
  163938. GABRIEL WEATHERHEAD
  163939. 10162N
  163940. 2/28/96V
  163941. A REVIEW. KAGAN, HENRI B.; SASAKI, MITSURU; COLLIN, JACQUELINE. ORGANIC CHEMISTRY WITH LANTHANIDES. 1988, 60(11),1725 30. PURE AND APPLIED CHEMISTRYa
  163942. GABRIEL WEATHERHEAD
  163943. 10163N
  163944. 2/28/96V
  163945. A REVIEW. SCOLASTICO, CARLO. ASYMMETRIC SYNTHESIS VIA NOREPHEDRINE DERIVED 2 ALKENYLOXAZOLIDINES. 1988, 60(11),1689 98. PURE AND APPLIED CHEMISTRY
  163946. GABRIEL WEATHERHEAD
  163947. 10164N
  163948. 2/28/96V
  163949. A REVIEW. CARDILLO, GIULIANA; ORENA, MARIO, SANDRI, SERGIO. STEREOCONTROLLED REACTIONS THROUGH HETEROCYCLIC INTERMEDIATES. 1988, 60(11), 1679 88. PURE AND APPLIED CHEMISTRYa
  163950. GABRIEL WEATHERHEAD
  163951. 10165N
  163952. 2/28/96V
  163953. A REVIEW. VIEHE, HEINZ G., MERENYI, ROBERT, JANOUSEK, ZDENEK. CAPTODATIVE SUBSTITUENT EFFECT. 45. CAPTODATIVE SUBSTITUENT EFFECTS IN RADICAL CHEMISTRY. 1988, 60(11),1635 44. PURE AND APPLIED CHEMISTRYa
  163954. GABRIEL WEATHERHEAD
  163955. 10166N
  163956. 2/28/96V
  163957. A REVIEW. TROST, BARRY M. TRANSITION METAL TEMPLATES AS GUIDE FOR CYCLOADDITIONS. 1988, 60(11),1615 26. PURE AND APPLIED CHEMISTRYa
  163958. GABRIEL WEATHERHEAD
  163959. 10167N
  163960. 2/28/96V
  163961. A REVIEW. DANISHEFSKY, SAMUEL J.; SIMONEAU, BRUNO. SYNTHETIC STUDIES IN THE MEVINOID FIELD. THE TOTAL SYNTHESIS OF ML236A. 1988, 60(11), 1555 62. PURE AND APPLIED CHEMISTRYa
  163962. GABRIEL WEATHERHEAD
  163963. 10168N
  163964. 2/28/96
  163965. A REVIEW. RAYMOND, KENNETH N.; MCMURRY, THOMAS J.; GARRETT, THOMAS M. MACROCYCLIC CATECHOL CONTAINING LIGANDS. 1988 60(4), 545 8. PURE AND APPLIED CHEMISTRYa
  163966. GABRIEL WEATHERHEAD
  163967. 10169N
  163968. 2/28/96V
  163969. A REVIEW. NICHOLSON, JEREMY K., WILSON, IAN D. HIGH RESOLUTION PROTON MAGNETIC RESONANCE SPECTROSCOPY OF BIOLOGICAL FLUIDS. 1989, 21(4 5), 449 501. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  163970. GABRIEL WEATHERHEAD
  163971. 10170N
  163972. 2/28/96V
  163973. A REVIEW. KRIVDIN, L. B., KALABIN, G. A. STRUCTURAL APPLICATIONS OF ONE BOND CARBON CARBON SPIN SPIN COUPLING CONSTNNTS. 1989, 21(4 5), 293 448. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPYa
  163974. GABRIEL WEATHERHEAD
  163975. 10171N
  163976. 2/28/96V
  163977. A REVIEW. JAMES, C. E.; HOUGH, L.; KHAN, R. SUCROSE AND ITS DERIVATIVES. 1989, 55, 117 184. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  163978. GABRIEL WEATHERHEAD
  163979. 10172N
  163980. 2/28/96
  163981. A REVIEW. LOUNASMAA, M.; GALAMBOS, J. INDOLE ALKALOID PRODUCTION IN C.ATHARQNTHUS ROSEUS CELL SUSPENSION CULTURES. 1989, 55, 89 115. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  163982. GABRIEL WEATHERHEAD
  163983. 10173N
  163984. 2/28/96V
  163985. A REVIEW. KROHN, K. BUILDING BLOCKS FOR THE TOTAL SYNTHESIS OF ANTHRACYCLINONES. 1989, 55, 37 88. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  163986. GABRIEL WEATHERHEAD
  163987. 10174N
  163988. 2/28/96V
  163989. A REVIEW. DAVIES COLEMAN, M. T.; RIVETT, D. E. A. NATURALLY OCCURRING 6 SUBSTITUTED 5,6 DIHYDRO A PYRONES. 1989, 55,1 35. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTSa
  163990. GABRIEL WEATHERHEAD
  163991. 10175N
  163992. 2/28/96V
  163993. A REVIEW. AL TALIB, MAHMOUD, TASHTOUSH, HASAN. RECENT ADVANCES IN THE USE OF ACYLIUM SALTS IN ORGANIC SYNTHESIS. L990, 22(1), 1 36. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163994. GABRIEL WEATHERHEAD
  163995. 10176N
  163996. 2/28/96
  163997. A REVIEW. HUNT, DAVID A. MICHAEL ADDITION OF ORGANOLITHIUM COMPOUNDS. A REVIEW. 1989, 21(6), 705 749. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  163998. GABRIEL WEATHERHEAD
  163999. 10177N
  164000. 2/28/96V
  164001. A REVIEW. MIYAKOSHI, TETSUO. PREPARATION AND REACTIONS OF 4 OXO CARBONYL COMPOUNDS. A REVIEW. 1989, 21(6), 659 704. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  164002. GABRIEL WEATHERHEAD
  164003. 10178N
  164004. 2/28/96V
  164005. A REVIEW. KAWADA, KENJI; KIM, MOONSUN; WAAT, DAVID S. SYNTHESIS OF QUASSINOIDS. A REVIEW. 1989, 21(5), 521 618. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  164006. GABRIEL WEATHERHEAD
  164007. 10179N
  164008. 2/28/96V
  164009. A REVIEW. RZESZOTARSKA, BARBARA, MASIUKIEWICZ, ELZBIETA. ARGININE HISTIDINE AND TRYPTOPHAN IN PEPTIDE SYNTHESIS. THE IMIDAZOLE FUNCTION OF HISTIDINE. , 21(4), 393 450. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  164010. GABRIEL WEATHERHEAD
  164011. 10180N
  164012. 2/28/96
  164013. A REVIEW. KOTALI, ANTIGONI, TSOUNGAS, PETROS G. PYRAZOLE L OXIDES 1,2 DIOXIDES AND DERIVATIVES. 1989, 29(8),1615 1648. HETEROCYCLESa
  164014. GABRIEL WEATHERHEAD
  164015. 10181N
  164016. 2/28/96V
  164017. A REVIEW. TOMINAGA, YOSHINORI, KOHRA, SHINYA, HONKAWA, HARUMASA; HOSOMI, AKIRA. SYNTHESIS OF PYRIMIDINE DERIVATIVES AND THEIR RELATED COMPOUNDS USING KETENE DITHIOACETALS. 1989, 29(7), 1409 1429. HETEROCYCLESa
  164018. GABRIEL WEATHERHEAD
  164019. 10182N
  164020. 2/28/96V
  164021. A REVIEW. CAPRARO, HANS GEORGE; LANG, MARC; SCHNEIDER, PETER. SYNTHESIS OF REGIOSPECIFICALLY SUBSTITUTED PYRIMIDYL DERIVATIVES AND THEIR INCORPORATION INTO PENEMS. 1989, 28(2), 643 652. HETEROCYCLESa
  164022. GABRIEL WEATHERHEAD
  164023. 10183N
  164024. 2/28/96V
  164025. A REVIEW. LERNER, RICHARD A., BENKOVIC, STEPHEN J. OBSERVATIONS IN THE INTERFACE BETWEEN IMMUNOCHEMISTRY AND CHEMISTRY. 1990, 3(1), 1 36. CHEMTRACTS: ORGANIC CHEMISTRYa
  164026. GABRIEL WEATHERHEAD
  164027. 10184N
  164028. 2/28/96
  164029. A REVIEW. REBEK, JULIUS, JR. RECOGNITION AND CATALYSIS USING MOLECULAR CLEFTS. 1989, 2(6), 337 52. CHEMTRACTS: ORGANIC CHEMISTRYa
  164030. GABRIEL WEATHERHEAD
  164031. 10185N
  164032. 2/28/96V
  164033. A REVIEW. DANISHEFSKY, SAMUEL. CYCLOADDITION AND CYCLOCONDENSATION REACTIONS OF HIGHLY FUNCTIONALIZED DIENES: APPLICATIONS TO ORGANIC SYNTHESIS. 1989, 2(5), 273 97. CHEMTRACTS: ORGANIC CHEMISTRYa
  164034. GABRIEL WEATHERHEAD
  164035. 10186N
  164036. 2/28/96V
  164037. A REVIEW. BERSON,JEROME A. REACTION SYMMETRY. CRITERIAIN THE DETECTION OF METASTABLE MECHANISTIC INTERMEDIATES: APPLICATION TO [1,3]  AND [3,3] SIGMATROPIC INTERMEDIATES. 1989, 2(4) 213 227 CHEMTRACTS: ORGANIC CHEMISTRYa
  164038. GABRIEL WEATHERHEAD
  164039. 10187N
  164040. 2/28/96VyA REVIEW. LAIRD, TREVOR. THE NEGLECTED SCIENCE OF CHEMICAL DEVELOPMENT. 1989, 25(12),1208 1211,1222. CHEMISTRY IN BRITAINa
  164041. GABRIEL WEATHERHEAD
  164042. 10188N
  164043. 2/28/96
  164044. PVhA REVIEW. NOYORI, RYOJI. PROSTAGLANDINS MADE SIMPLE. 1989, 25(9), 883 884, 887 888. CHEMISTRY IN BRITAINa
  164045. GABRIEL WEATHERHEAD
  164046. 10189N
  164047. 2/28/96VwA REVIEW. CHRISTENSEN, B. G. TIENAM
  164048. FROM NATURAL PRODUCT TO ANTIBIOTIC. 1989, 26(4), 371 372, 374. CHEMISTRY IN BRITAINa
  164049. GABRIEL WEATHERHEAD
  164050. 10190N
  164051. 2/28/96VtA REVIEW. FLEET, GEORGE W. J. HOMOCHIRAL COMPOUNDS FROM SUGARS. 1989, 25(3), 287, 289 290, 292. CHEMISTRY IN BRITAINa
  164052. GABRIEL WEATHERHEAD
  164053. 10191N
  164054. 2/28/96V
  164055. A REVIEW. WESTWOOD, NICHOLAS P., C. ULTRAVIOLET PHOTOELECTRON STUDIES OF UNSTABLE MOLECULES WITH RELEVANCE TO SYNTHESIS, QUANTUM CHEMISTRY, AND SPECTROSCOPY. 1989, 18(3), 317 45. CHEMICAL SOCIETY REVIEWSa
  164056. GABRIEL WEATHERHEAD
  164057. 10192N
  164058. 2/28/96V
  164059. A REVIEW. RANDACCIO, L.; PAHOR, N. BRESCIANI; ZANGRANDO, E.; MARZILLI, L. G. STRUCTURAL PROPERTIES OF ORGANOCOBALT COENZYME BL2 MODELS. 1989, 18(2), 225 50. CHEMICAL SOCIETY REVIEWSa
  164060. GABRIEL WEATHERHEAD
  164061. 10193N
  164062. 2/28/96V
  164063. A REVIEW. GREBENIK, PETER; GRINTER, ROGER, PERUTZ, ROBIN N. METALLOCENES AS REACTION INTERMEDIATES. 1988, 17(4), 453 90. CHEMICAL SOCIETY REVIEWSa
  164064. GABRIEL WEATHERHEAD
  164065. 10194N
  164066. 2/28/96V
  164067. A REVIEW. RYABOV, ALEXANDER D. MECHANISMS OF INTRAMOLECULAR ACTIVATION OF CARBON HYDROGEN BONDS IN TRANSITION METAL COMPLEXES. 1990, 90(2), 403 424. CHEMICAL REVIEWSa
  164068. GABRIEL WEATHERHEAD
  164069. 10195N
  164070. 2/28/96V
  164071. A REVIEW. BARRAU, JACQUES; ESCUDIE, JEAN; SATGE, JACQUES. MULTIPLY BONDED GERMANIUM SPECIES. RECENT DEVELOPMENTS. 1990, 90(1), 283 319. CHEMICAL REVIEWSa
  164072. GABRIEL WEATHERHEAD
  164073. 10196N
  164074. 2/28/96V
  164075. A REVIEW. COLOMER, ERNEST CORRIU, ROBERT J. P., LHEUREUX, MARC. GROUP 14 METALLOLES. 2. IONIC SPECIES AND COORDINATION COMPOUNDS. 1990, 90(1), 265 282. CHEMICAL REVIEWSa
  164076. GABRIEL WEATHERHEAD
  164077. 10197N
  164078. 2/28/96
  164079. A REVIEW. DUBAC, JACQUES; LAPORTERIE, ANDRE; MANUEL, GEORGES. GROUP 14 METALLOLES. 1. SYNTHESIS, ORGANIC CHEMISTRY, AND PHYSICOCHEMICAL DATA. 1990, 90(1), 215 263. CHEMICAL REVIEWSa
  164080. GABRIEL WEATHERHEAD
  164081. 10198N
  164082. 2/28/96V|A REVIEW. REGITZ, MANFRED. PHOSPHAALKYNES: NEW BUILDING BLOCKS IN SYNTHETIC CHEMISTRY. 1990, 90(1),191 213. CHEMICAL REVIEWSa
  164083. GABRIEL WEATHERHEAD
  164084. 10199N
  164085. 2/28/96V
  164086. A REVIEW. DIMAIO, ANTHONY JOSEPH; RHEINGOLD, ARNOLD L. STRUCTURAL CHEMISTRY OF TRANSITION METAL COMPLEXES CONTAINING ARSENIC ARSENIC BONDS. 1990, 90(1), 169 190. CHEMICAL REVIEWSa
  164087. GABRIEL WEATHERHEAD
  164088. 10200N
  164089. 2/28/96V
  164090. A REVIEW. HOLMES, ROBERT R. THE STEREOCHEMISTRY OF NUCLEOPHILIC SUBSTITUTION OF TETRACOORDINATE SILICON. 1990, 90(1),17 31. CHEMICAL REVIEWSa
  164091. GABRIEL WEATHERHEAD
  164092. 10201N
  164093. 2/28/96VdA REVIEW. VEITH, MICHAEL. CAGE COMPOUNDS WITH MAIN GROUP METALS. 1990, 90(1), 3 16. CHEMICAL REVIEWSa
  164094. GABRIEL WEATHERHEAD
  164095. 10202N
  164096. 2/28/96VsA REVIEW. ERDIK, ENDER; AY, MEHMET. ELECTROPHILIC AMINATION OF CARBANIONS. 1989, 89(8), 1947 1980. CHEMICAL REVIEWSa
  164097. GABRIEL WEATHERHEAD
  164098. 10203N
  164099. 2/28/96V
  164100. A REVIEW. REBEK, JULIUS, JR. MOLECULAR RECOGNITION WITH MODEL SYSTEMS. 1990, 29(3), 245 55. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164101. GABRIEL WEATHERHEAD
  164102. 10204N
  164103. 2/28/96
  164104. A REVIEW. ZENNECK, ULRICH. REACTIVE P COMPLEXES OF ELECTRON RICH TRANSITION METALS. 10. HIGHLY REACTIVE INTERMEDIATES FROM CO CONDENSATION REACTIONS OF IRON, COBALT AND NICKEL VAPORS WITH ARENES. 1990, 29(2),126 37. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  164105. GABRIEL WEATHERHEAD
  164106. 10205N
  164107. 2/28/96V
  164108. A REVIEW. STRAZEWSKI, PETER; TAMM, CHRISTOPH. REPLICATION EXPERIMENTS WITH NUCLEOTIDE BASE ANALOGS. 1990, 29(1), 36 57. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164109. GABRIEL WEATHERHEAD
  164110. 10206
  164111. 2/28/96V
  164112. A REVIEW. BOCK, HANS. FUNDAMENTALS OF SILICON CHEMISTRY. MOLECULAR STATES OF SILICON CONTAINING COMPOUNDS. 1989, 28(12), 1627 50. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164113. GABRIEL WEATHERHEAD
  164114. 10207N
  164115. 2/28/96V
  164116. A REVIEW. WACHTER, JOACHIM. SYNTHESIS, STRUCTURE AND REACTIVITY OF SULFUR RICH CYCLOPENTADIENYL TRANSITION METAL COMPLEXES: SULFUR CHEMISTRY FROM AN ORGANOMETALLIC POINT OF VIEW. 1989, 28(12), 1613 26. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164117. GABRIEL WEATHERHEAD
  164118. 10208N
  164119. 2/28/96V
  164120. A REVIEW. LAMMERTSMA, KOOP; SCHLEYER, PAUL V. R.; SCHWARZ, HELMUT. ORGANIC DICATIONS: GAS PHASE EXPERIMENTS AND THEORY IN CONCERT. 1989, 28(10),1321 41. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164121. GABRIEL WEATHERHEAD
  164122. 10209N
  164123. 2/28/96
  164124. A REVIEW. BENNETT, MARTIN A.; SCHWEMLEIN, HEINZ P. METAL COMPLEXES WITH SMALL CYCLOALKYNES AND ARYNES. 1989, 28(10), 1296 1320. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164125. GABRIEL WEATHERHEAD
  164126. 10210N
  164127. 2/28/96V{A REVIEW. SCHULZ, PETER G. CATALYTIC ANTIBODIES. 1989, 28(10), 1283 95. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164128. GABRIEL WEATHERHEAD
  164129. 10211N
  164130. 2/28/96V
  164131. A REVIEW. TROST, BARRY M. CYCLIZATIONS VIA PALLADIUM CATALYZED ALLYLIC AIKYLATION. 1989, 28(9),1173 92. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164132. GABRIEL WEATHERHEAD
  164133. 10212N
  164134. 2/28/96V
  164135. A REVIEW. HAALAND, ARNE. COVALENT VERSUS DATIVE BONDS TO MAIN GROUP METALS: A USEFUL DIFFERENCE. 1989, 28(8), 992 1007. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164136. GABRIEL WEATHERHEAD
  164137. 10213N
  164138. 2/28/96
  164139. A REVIEW. GIESE, BERND. STEREOSELECTIVITY OF INTERMOLECULAR FREE RADICAL REACTIONS. 1989, 28(8), 969 80. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164140. GABRIEL WEATHERHEAD
  164141. 10214N
  164142. 2/28/96V
  164143. A REVIEW. QUACK, MARTIN. STRUCTURE AND DYNAMICS OF CHIRAL MOLECULES. 1989, 28(5), 571 86. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164144. GABRIEL WEATHERHEAD
  164145. 10215N
  164146. 2/28/96V
  164147. A REVIEW. PETER, MARTIN G. CHEMICAL MODIFICATION OF BIOPOLYMERS WITH QUINONES AND QUINONE METHIDES. 1989, 28(5), 555 70. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164148. GABRIEL WEATHERHEAD
  164149. 10216N
  164150. 2/28/96V
  164151. A REVIEW. MUTTER, MANFRED; VUILLEUMIER, STEPHANE. A CHEMICAL APPROACH TO PROTEIN SYNTHESIS: TEMPLATE ASSEMBLED SYNTHETIC PROTEINS (TASP). 1989, 28(5), 535 554. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  164152. GABRIEL WEATHERHEAD
  164153. 10217N
  164154. 2/28/96
  164155. >A REVIEW. CHISHOLM, MALCOLM H.; CLARK, DAVID L., HAMPDEN SMITH MARK J.; HOFFMAN, DAVID M. ALKOXIDE CLUSTERS OF MOLYBDENUM AND TUNGSTEN AS TEMPLATES FOR ORGANOMETALLIC CHEMISTRY; COMPARISON WITH CARBONYL CLUSTERS OF THE LATER TRANSITION ELEMENTS. 1989, 28(4), 432 44. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  164156. GABRIEL WEATHERHEAD
  164157. 10218N
  164158. 2/28/96V
  164159. A REVIEW. BALLESTER, M. PERCHLORO ORGANIC CHEMISTRY: STRUCTURES, SPECTROSCOPY AND REACTION PATHWAYS. 1989, 25, 267 445. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  164160. GABRIEL WEATHERHEAD
  164161. 10219N
  164162. 2/28/96V
  164163. A REVIEW. THATCHER, GREGORY, R. J.; KLUGER, RONALD. MECHANISM AND CATALYSIS OF NUCLEOPHILIC SUBSTITUTION IN PHOSPHATE ESTERS. 1989, 25, 99 265. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  164164. GABRIEL WEATHERHEAD
  164165. 10220N
  164166. 2/28/96
  164167. A REVIEW. BERG, ULF; SANDSTROM, JAN. STERIC AND DYNAMIC STEREOCHEMISTRY OF ALKYL AND ANALOGOUS GROUPS. 1989, 25,1 97. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  164168. GABRIEL WEATHERHEAD
  164169. 10221N
  164170. 2/28/96VdA REVIEW. PERLMUTTER, HOWARD D. 1,4 DIAZOCINES. 1989, 45,185 229. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164171. GABRIEL WEATHERHEAD
  164172. 10222N
  164173. 2/28/96V
  164174. A REVIEW. PORTER, ALEXANDER E. A. THE CHEMISTRY OF THIOPHENIUM SALTS AND THIOPHENIUM YLIDES. 1989, 45,151 184. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164175. GABRIEL WEATHERHEAD
  164176. 10223N
  164177. 2/28/96VcA REVIEW. TISLER, MIHA. HETEROCYCLIC QUINONES. 1989, 45, 37 150. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164178. GABRIEL WEATHERHEAD
  164179. 10224N
  164180. 2/28/96V
  164181. A REVIEW. FUJITA, EIICHI; NAGAO, YOSHIMITSU. CHIRAL INDUCTION USING HETEROCYCLES. 1989, 45 1  36. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164182. GABRIEL WEATHERHEAD
  164183. 10225N
  164184. 2/28/96
  164185. A REVIEW. ETTER, MARGARET C. ENCODING AND DECODING HYDROGEN BOND PATTERNS OF ORGANIC COMPOUNDS. 1990, 23(4),120 126. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164186. GABRIEL WEATHERHEAD
  164187. 10226N
  164188. 2/28/96V
  164189. A REVIEW. KLIBANOV, ALEXANDER M. ASYMMETRIC TRANSFORMATIONS CATALYZED BY ENZYMES IN ORGANIC SOLVENTS. 1990, 23(4), 114 120 A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164190. GABRIEL WEATHERHEAD
  164191. 10227N
  164192. 2/28/96V
  164193. A REVIEW. HOUK, KENDALL N.; TUCKER, JOHN A.; DORIGO, ANDREA E. QUANTITATIVE MODELING OF PROXIMITY EFFECTS ON ORGANIC REACTIVITY. 1990, 23(4), 107 13. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164194. GABRIEL WEATHERHEAD
  164195. 10228N
  164196. 2/28/96V
  164197. A REVIEW. RUASSE, MARIE FRANCOISE. BROMONIUM IONS OR B BROMOCARBOCATIONS IN OLEFIN BROMINATION. A KINETIC APPROACH TO PRODUCT SELECTIVITIES. 1990, 23(3), 87 93. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164198. GABRIEL WEATHERHEAD
  164199. 10229N
  164200. 2/28/96
  164201. A REVIEW. POULTER C. DALE. BIOSYNTHESIS OF NON HEAD TO TAIL TERPENES. FORMATION OF 1' 1 AND 1' 3 LINKAGES. 1990, 23(3), 70 77. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164202. GABRIEL WEATHERHEAD
  164203. 10230N
  164204. 2/28/96V
  164205. A REVIEW. HOSOKAWA, TAKAHIRO; MURAHASHI, SHUN ICHI. NEW ASPECTS OF OXYPALLADATION OF ALKENES. 1990, 23(2), 49 54. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164206. GABRIEL WEATHERHEAD
  164207. 10231N
  164208. 2/28/96V
  164209. A REVIEW. KRESGE, A. JERRY. FLASH PHOTOLYTIC GENERATION AND STUDY OF REACTIVE SPECIES: FROM ENOLS TO YNOLS. 1990, 23(2), 43 48. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164210. GABRIEL WEATHERHEAD
  164211. 10232N
  164212. 2/28/96V
  164213. A REVIEW. TROST, BARRY M. PALLADIUM CATALYZED CYCLOISOMERIZATION OF ENYNES AND RELATED REACTIONS. 1990, 23(2), 34 42. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164214. GABRIEL WEATHERHEAD
  164215. 10233N
  164216. 2/28/96
  164217. A REVIEW. WERNER, HELMUT; ERKER, GERHARD, EDS. ORGANOMETALLICS IN ORGANIC SYNTHESIS. 2. ASPECTS OF A MODERN INTERDISCIPLINARY FIELD. SPRINGER VERLAG: BERLIN, 1989.a
  164218. GABRIEL WEATHERHEAD
  164219. 10234N
  164220. 2/28/96VWA REVIEW. TAYLOR,R. ELECTROPHILIC AROMATIC SUBSTITUTION. WILEY: CHICHESTER, U.K., 1990.a
  164221. GABRIEL WEATHERHEAD
  164222. 10235N
  164223. 2/28/96VXA REVIEW. STEVENSON, D.; WILSON, I. D., EDS. CHIRAL SEPARATIONS. PLENUM: NEW YORK, 1988.a
  164224. GABRIEL WEATHERHEAD
  164225. 10236N
  164226. 2/28/96VqA REVIEW. SOUTHON, I. W., BUCKINGHAM, J., EDS. DICTIONARY OF ALKALOIDS. 2 VOLS. CHAPMAN AND HALL: NEW YORK, 1989.a
  164227. GABRIEL WEATHERHEAD
  164228. 10237N
  164229. 2/28/96VSA REVIEW. SCHUETZ,H. BENZODIAZEPINES II. A HANDBOOK. SPRINGER VERLAG: BERLIN, 1989.a
  164230. GABRIEL WEATHERHEAD
  164231. 10238N
  164232. 2/28/96V
  164233. A REVIEW. RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 6: STEREOSELECTIVE SYNTHESIS, PART D. ELSEVIER: AMSTERDAM 1990.
  164234. GABRIEL WEATHERHEAD
  164235. 10239N
  164236. 2/28/96V
  164237. A REVIEW. PELYVAS, I. F.; MONNERET, C.; HERCZEGH, P. SYNTHETIC ASPECTS OF AMINODEOXY SUGARS OF ANTIBIOTICS. SPRINGER VERLAG: BERLIN, 1988.a
  164238. GABRIEL WEATHERHEAD
  164239. 10240N
  164240. 2/28/96V
  164241. A REVIEW. MORRISON, HARRY, ED. BIOORGANIC PHOTOCHEMISTRY (VOL. 1). PHOTOCHEMISTRY AND THE NUCLEIC ACIDS. WILEY: NEW YORK, 1990.a
  164242. GABRIEL WEATHERHEAD
  164243. 10241N
  164244. 2/28/96VwA REVIEW. LOUGH, W. J., ED. CHIRAL LIQUID CHROMATOGRAPHY. BLACKIE: GLASGOW, U.K., AND CHAPMAN AND HALL: NEW YORK, 1989.a
  164245. GABRIEL WEATHERHEAD
  164246. 10242N
  164247. 2/28/96V
  164248. A REVIEW. LLOYD, DOUGLAS, ED. THE CHEMISTRY OF CONJUGATED COMPOUNDS. TO BE OR NOT TO BE LIKE BENZENE. WILEY: CHICHESTER, U.K., 1989.a
  164249. GABRIEL WEATHERHEAD
  164250. 10243N
  164251. 2/28/96V
  164252. A REVIEW. KATAWALA, F. G.; COPPOLA, GARY M.; SCHUSTER, HERBERT F.; EDS. ISOQUINOLINES, PART 2 (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 38). WILEY: NEW YORK, 1990.
  164253. GABRIEL WEATHERHEAD
  164254. 10244N
  164255. 2/28/96V
  164256. A REVIEW. JONES, R. ALAN, ED. PYRROLES. PART 1. THE SYNTHESIS AND THE PHYSICAL AND CHEMICAL ASPECTS OF THE PYRROLE RING (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 48, PART 1). WILEY: NEW YORK, 1990.a
  164257. GABRIEL WEATHERHEAD
  164258. 10245N
  164259. 2/28/96V
  164260. A REVIEW. HARTLEY, FRANK R., ED. THE CHEMISTRY OF THE METAL CARBON BOND, VOL. 5: ORGANOMETALLIC COMPOUNDS IN ORGANIC AND BIOLOGICAL SYNTHESES. WILEY: CHICHESTER, U.K., 1989.a
  164261. GABRIEL WEATHERHEAD
  164262. 10246N
  164263. 2/28/96V[A REVIEW. HARRINGTON, PETER J. TRANSITION METALS IN TOTAL SYNTHESIS. WILEY: NEW YORK, 1990.a
  164264. GABRIEL WEATHERHEAD
  164265. 10247N
  164266. 2/28/96VCA REVIEW. GILCHRIST,T. HETEROCYCLIC CHEMISTRY. WILEY: NEWYORK 1989.a
  164267. GABRIEL WEATHERHEAD
  164268. 10248N
  164269. 2/28/96V
  164270. A REVIEW. FEUER, HENRY; NIELSEN, ARNOLD T., EDS. NITRO COMPOUNDS. RECENT ADVANCES AND SYNTHESES AND CHEMISTRY. VCH: NEW YORK, 1990.a
  164271. GABRIEL WEATHERHEAD
  164272. 10249N
  164273. 2/28/96V
  164274. A REVIEW. EL'TSOV, A. V. ORGANIC PHOTOCHROMES (TRANSLATED BY Y. E. SVIRIDOV, J. WHITALL, TRANSLATION ED.), CONSULTANTS BUREAU, NEW YORK, 1990.a
  164275. GABRIEL WEATHERHEAD
  164276. 10250N
  164277. 2/28/96V
  164278. A REVIEW. DOLPHIN, DAVID; AVRAMOVIC, OLGA, POULSON, ROZANNE, EDS. GLUTATHIONE: CHEMICAL, BIOCHEMICAL AND MEDICAL ASPECTS. 2 VOLS. (COENZYMES AND COFACTORS, VOL. 3) WILEY: NEW YORK, 1989.a
  164279. GABRIEL WEATHERHEAD
  164280. 10251N
  164281. 2/28/96V
  164282. A REVIEW. CRIPPA, R., HORAK, V.; PROTN, G.; SVORONOS, P.; WOLFRAM, L. CHEMISTRY OF MELANINS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164283. GABRIEL WEATHERHEAD
  164284. 10252N
  164285. 2/28/96V
  164286. A REVIEW. TAKANO, 5., OGASAWARA, K. ALKALOIDS OF THE CALABAR BEAN. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164287. GABRIEL WEATHERHEAD
  164288. 10253N
  164289. 2/28/96
  164290. A REVIEW. KAMETANI, T., KOIZUMI, M. PHENETHYLISOQUINOLINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164291. GABRIEL WEATHERHEAD
  164292. 10254N
  164293. 2/28/96V
  164294. A REVIEW. OHMOTO, T.; KOIKE, K. CANTHIN 6 ONE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164295. GABRIEL WEATHERHEAD
  164296. 10255N
  164297. 2/28/96V
  164298. A REVIEW. HOSHINO, 0., UMEZAWA, B. LEAD TETRAACETATE OXIDATION IN ALKALOID SYNTHESIS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164299. GABRIEL WEATHERHEAD
  164300. 10256N
  164301. 2/28/96V
  164302. A REVIEW. AIMI, N.; SAKAI, 5.; BAN, Y. ALKALOIDS OF STRYCHNOS AND GARDNERIA SPECIES. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY VOLUME 36, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164303. GABRIEL WEATHERHEAD
  164304. 10257N
  164305. 2/28/96
  164306. A REVIEW. JACOBS, H. M.; BURKE, B. A. OXAZOLE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164307. GABRIEL WEATHERHEAD
  164308. 10258N
  164309. 2/28/96V
  164310. A REVIEW. CYBULSKI, J.; WROBEL, J. T. NUPHAR ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164311. GABRIEL WEATHERHEAD
  164312. 10259N
  164313. 2/28/96V
  164314. A REVIEW. CASTEDO, L.; DOMINGUEZ, D. DIBENZAZONINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164315. GABRIEL WEATHERHEAD
  164316. 10260N
  164317. 2/28/96V
  164318. A REVIEW. FUJI, K. LYTHRACEOUS ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164319. GABRIEL WEATHERHEAD
  164320. 10261N
  164321. 2/28/96
  164322. A REVIEW. LUNDSTROM, J. ,B PHENETHYLAMINES AND EPHEDRINES OF PLANT ORIGIN. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164323. GABRIEL WEATHERHEAD
  164324. 10262N
  164325. 2/28/96V
  164326. A REVIEW. CAVE, A.; LEBOEUF, M.; CASSELS, B. K. ALKALOIDS FROM GUATTETIA. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 35, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1989.a
  164327. GABRIEL WEATHERHEAD
  164328. 10263N
  164329. 2/28/96V
  164330. A REVIEW. VERPOORTE, R.; SCHRIPSEMA, J.; VAN DER LEER, T. CINCHONA ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164331. GABRIEL WEATHERHEAD
  164332. 10264N
  164333. 2/28/96V
  164334. A REVIEW. MASSIOT, G.; DELAUDE, C. AFRICAN STRYCHNOS ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164335. GABRIEL WEATHERHEAD
  164336. 10265N
  164337. 2/28/96
  164338. A REVIEW. ONDA, M., TAKAHASHI, H. PROTOPINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164339. GABRIEL WEATHERHEAD
  164340. 10266N
  164341. 2/28/96V
  164342. A REVIEW. AMIYA, T.; BANDO, H. ACONITUM ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164343. GABRIEL WEATHERHEAD
  164344. 10267N
  164345. 2/28/96V
  164346. A REVIEW. MECHOULAM, R. ALKALOIDS IN CANNABIS SATIVA L. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164347. GABRIEL WEATHERHEAD
  164348. 10268N
  164349. 2/28/96V
  164350. A REVIEW. HINO, T.; NAKAGAWA, M. CHEMISTRY AND REACTIONS OF CYCLIC TAUTOMERS OF TRYPTAMINES AND TRYPTOPHANS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 34, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164351. GABRIEL WEATHERHEAD
  164352. 10269N
  164353. 2/28/96
  164354. A REVIEW. MATSUI, M. HASUBANAN ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 33, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164355. GABRIEL WEATHERHEAD
  164356. 10270N
  164357. 2/28/96V
  164358. A REVIEW. ROZWADOWSKA, M. D. SECOISOQUINOLINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 33, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164359. GABRIEL WEATHERHEAD
  164360. 10271N
  164361. 2/28/96V
  164362. A REVIEW. HANAOKA, M. TRANSFORMATION REACTIONS OF PROTOBERBERINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 33, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164363. GABRIEL WEATHERHEAD
  164364. 10272N
  164365. 2/28/96V
  164366. A REVIEW. LIU, Z. H.; LU, R. R. GELSEMIUM ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 33, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164367. GABRIEL WEATHERHEAD
  164368. 10273N
  164369. 2/28/96
  164370. A REVIEW. LOUNASMAA, M. THE TROPANE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY, VOLUME 33, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1988.a
  164371. GABRIEL WEATHERHEAD
  164372. 10274N
  164373. 2/28/96
  164374. dA REVIEW. BOGER, DALE L.; BROTHERTON PLEISS, CHRISTINE E. THERMAL REACTION OF CYCLOPROPANONE KETAL. KEY MECHNNISTIC FEATURES. SCOPE AND APPLICATIONS OF THE CYCLOADDITION REACTIONS OF CYCLOPROPANONE KETALS AND PI DELOCALIZED VINYL CARBENES: THREE CARBON 1, /1,3 DIPOLES. ADVANCES IN CYCLOADDITION, VOLUME 2 D. P. CURRAN, ED., JAI PRESS: GREENWICH, CT, 1990.
  164375. GABRIEL WEATHERHEAD
  164376. 10275N
  164377. 2/28/96V
  164378. A REVIEW. ROUSH, WILLIAM R. STEREOCHEMICAL AND SYNTHETIC STUDIES OF THE INTRAMOLECULAR DIELS ALDER REACTION. ADVANCES IN CYCLOADDITION, VOLUME 2 D. P. CURRAN, ED., JAI PRESS: GREENWICH, CT, 1990.a
  164379. GABRIEL WEATHERHEAD
  164380. 10276N
  164381. 2/28/96
  164382. A REVIEW. PADWA, ALBERT; SCHOFFSTALL, ALLEN M. INTRAMOLECULAR 1,3 DIPOLAR CYCLOADDITION CHEMISTRY. ADVANCES IN CYCLOADDITION, VOLUME 2 D. P. CURRAN, ED., JAI PRESS: GREENWICH, CT, 1990.a
  164383. GABRIEL WEATHERHEAD
  164384. 10277N
  164385. 2/28/96V
  164386. A REVIEW. EL BASIL, SHERIF. CATERPILLAR (GUTMAN) TREES IN CHEMICAL GRAPH THEORY. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 273 89. TOPICS IN CURRENT CHEMISTRYa
  164387. GABRIEL WEATHERHEAD
  164388. 10278N
  164389. 2/28/96V
  164390. A REVIEW. HOSOYA, HARUO. CLAR'S AROMATIC SEXTET AND SEXTET POLYNOMIAL. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 255 72. TOPICS IN CURRENT CHEMISTRYa
  164391. GABRIEL WEATHERHEAD
  164392. 10279N
  164393. 2/28/96
  164394. A REVIEW. CHEN, RONGSI; CYVIN, S. J.; CYVIN, B. N.; BRUNVOLL, J.; KLEIN, D. J. METHODS OF ENUMERATING KEKULE STRUCTURES, EXEMPLIFIED BY APPLICATIONS TO RECTANGLE SHAPED BENZENOIDS. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 227 53. TOPICS IN CURRENT CHEMISTRY
  164395. GABRIEL WEATHERHEAD
  164396. 10280N
  164397. 2/28/96V
  164398. A REVIEW. SHENG, RONGQIN. RAPID WAYS TO RECOGNIZE KEKULEAN BENZENOID SYSTEMS. 1990, 153 (ADV. THEORY BENZENOID HYDROCARBONS) 211 26. TOPICS IN CURRENT CHEMISTRYa
  164399. GABRIEL WEATHERHEAD
  164400. 10281N
  164401. 2/28/96V
  164402. A REVIEW. HE, WENCHEN, HE, WENJIE. PEAK VALLEY PATH METHOD ON BENZENOID AND CORONOID SYSTEMS. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 195 209. TOPICS IN CURRENT CHEMISTRYa
  164403. GABRIEL WEATHERHEAD
  164404. 10282N
  164405. 2/28/96V
  164406. A REVIEW. ZHANG, FUJI; GUO, XIAOFENG, CHEN, RONGSI. THE EXISTENCE OF KEKULE STRUCTURES IN A BENZENOID SYSTEM. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 181 93. TOPICS IN CURRENT CHEMISTRYa
  164407. GABRIEL WEATHERHEAD
  164408. 10283N
  164409. 2/28/96
  164410. A REVIEW. JOHN, PETER; SACHS, HORST. CALCULATING THE NUMBERS OF PERFECT MATCHINGS AND OF SPANNING TREES, PAULING'S ORDERS, THE CHARACTERISTIC POLYNOMIAL, AND THE EIGENVECTORS OF A BENZENOID SYSTEM. 1990, 153 (ADV. THEORY BENZENOID HYDROCARBONS), 145 79. TOPICS IN CURRENT CHEMISTRY
  164411. GABRIEL WEATHERHEAD
  164412. 10284N
  164413. 2/28/96V
  164414. A REVIEW. DIAS, JERRY RAY. A PERIODIC TABLE FOR BENZENOID HYDROCARBONS. 1990, 153 (ADV. THEORY BENZENOID HYDROCARBONS), 123 43. TOPICS IN CURRENT CHEMISTRYa
  164415. GABRIEL WEATHERHEAD
  164416. 10285N
  164417. 2/28/96V
  164418. A REVIEW. ZANDER, MAXIMILIAN. MOLECULAR TOPOLOGY AND CHEMICAL REACTIVITY OF POLYNUCLEAR BENZENOID HYDROCARBONS. 1990 153 (ADV. THEORY BENZENOID HYDROCARBONS), 101 22. TOPICS IN CURRENT CHEMISTRYa
  164419. GABRIEL WEATHERHEAD
  164420. 10286N
  164421. 2/28/96V
  164422. A REVIEW. CIOSLOWSKI, JERZY. SCALING PROPERTIES OF TOPOLOGICAL INVARIANTS. 1990 153 (ADV. THEORY BENZENOID HYDROCARBONS), 85 99 TOPICS IN CURRENT CHEMISTRY
  164423. GABRIEL WEATHERHEAD
  164424. 10287N
  164425. 2/28/96V
  164426. A REVIEW. KLEIN, DOUGLAS J. SEMIEMPIRICAL VALENCE BOND VIEWS FOR BENZENOID HYDROCARBONS. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 57 83. TOPICS IN CURRENT CHEMISTRYa
  164427. GABRIEL WEATHERHEAD
  164428. 10288N
  164429. 2/28/96V
  164430. A REVIEW. COOPER, DAVID L., GERRATT, JOSEPH, RAIMONDI, MARIO. THE SPIN COUPLED VALENCE BOND DESCRIPTION OF BENZENOID AROMATIC MOLECULES. 1990,153 (ADV. THEORY BENZENOID HYDROCARBONS), 41 55. TOPICS IN CURRENT CHEMISTRYa
  164431. GABRIEL WEATHERHEAD
  164432. 10289N
  164433. 2/28/96V
  164434. A REVIEW. HIBERTY, PHILIPPE CHARLES. THE DISTORTIVE TENDENCIES OF DELOCALIZED P ELECTRONIC SYSTEMS. BENZENE, CYCLOBUTADIENE, AND RELATED HETEROANNULENES. 1990, 153 (ADV. THEORY BENZENOID HYDROCARBONS), 27 39. TOPICS IN CURRENT CHEMISTRYa
  164435. GABRIEL WEATHERHEAD
  164436. 10290N
  164437. 2/28/96
  164438. A REVIEW. SCHAFER, HANS JURGEN. RECENT CONTRIBUTIONS OF KOLBE ELECTROLYSIS TO ORGANIC SYNTHESIS. 1990, 152 (ELECTROCHEMISTRY 4), 91 151. TOPICS IN CURRENT CHEMISTRYa
  164439. GABRIEL WEATHERHEAD
  164440. 10291N
  164441. 2/28/96V~A REVIEW. STRAZZOLINI, PAOLO; GIUMANINI, ANGELO G.; CAUCI, SABINA. ACETIC FORMIC ANHYDRIDE. 1990, 46(4), 1081 118. TETRAHEDRONa
  164442. GABRIEL WEATHERHEAD
  164443. 10292N
  164444. 2/28/96VVA REVIEW. ALDER, ROGER W. INTRABRIDGEHEAD CHEMISTRY. 1990, 46(3), 683 713. TETRAHEDRONa
  164445. GABRIEL WEATHERHEAD
  164446. 10293N
  164447. 2/28/96V
  164448. A REVIEW. NISHIO, MOTOHIRO; HIROTA, MINORU. CH/P INTERACTION: IMPLICATIONS IN ORGANIC CHEMISTRY. 1989, 45(23), 7201 45. TETRAHEDRONa
  164449. GABRIEL WEATHERHEAD
  164450. 10294N
  164451. 2/28/96VdA REVIEW. TRUCE, WILLIAM E. FORTY YEARS IN ORGANOSULFUR CHEMISTRY. 1990, 9(4), 351 7. SULFUR REPORTSa
  164452. GABRIEL WEATHERHEAD
  164453. 10295N
  164454. 2/28/96
  164455. A REVIEW. FREEMAN, FILLMORE; KIM, DARRICK S. H. L.; RODRIGUEZ, ELOY. THE CHEMISTRY OF 1,2 DITHIINS. 1989, 9(3), 207 56. SULFUR REPORTSa
  164456. GABRIEL WEATHERHEAD
  164457. 10296N
  164458. 2/28/96VjA REVIEW. LOZAC'H, NOEL. FORTY YEARS OF HETEROCYCLIC SULFUR CHEMISTRY. 1989, 9(3), 153 206. SULFUR REPORTSa
  164459. GABRIEL WEATHERHEAD
  164460. 10297N
  164461. 2/28/96V
  164462. A REVIEW. GUSAROVA, N. K.; VORONKOV, M. G.; TROFIMOV, B. A. DIVINYL SULFOXIDE: SYNTHESIS, PROPERTIES, AND APPLICATIONS. 1989, 9(2), 95 141. SULFUR REPORTSa
  164463. GABRIEL WEATHERHEAD
  164464. 10298N
  164465. 2/28/96V
  164466. A REVIEW. MIRSKOVA, A. N.; SEREDKINA, S. G.; VORONKOV, M. G. (ORGANOTHIO)CHLOROACETYLENES, NEW POLYFUNCTIONAL REAGENTS FOR ORGANIC SYNTHESIS. 1989, 9(2), 75 90. SULFUR REPORTSa
  164467. GABRIEL WEATHERHEAD
  164468. 10299N
  164469. 2/28/96
  164470. A REVIEW. CHAUSSARD, JACQUES, FOLEST, JEAN CLAUDE, NEDELEC, JEAN YVES; PERICHON, JACQUES; SIBILLE, SOLINE; TROUPEL, MICHEL. USE OF SACRIFICIAL ANODES IN ELECTROCHEMICAL FUNCTIONALIZATION OF ORGANIC HALIDES. 1990, NO. 5, 369 81. SYNTHESISa
  164471. GABRIEL WEATHERHEAD
  164472. 10300N
  164473. 2/28/96VvA REVIEW. KOLB, MICHAEL. KETENE DITHIOACETALS IN ORGANIC SYNTHESIS: RECENT DEVELOPMENTS. 1990, NO. 3,171 90. SYNTHESISa
  164474. GABRIEL WEATHERHEAD
  164475. 10301N
  164476. 2/28/96V
  164477. A REVIEW. LUH, TIEN YAU; NI, ZHI JIE. TRANSITION METAL MEDIATED CARBON SULFUR BOND CLEAVAGE REACTIONS. 1990, NO. 2, 89 130. SYNTHESISa
  164478. GABRIEL WEATHERHEAD
  164479. 10302N
  164480. 2/28/96V
  164481. A REVIEW. SCHICK, HANS  EICHHORN, INGE. SYNTHESES AND REACTIONS OF 2 ALKYL 1,3 CYCLOPENTANEDIONES (2 ALKYL 3 HYDROXY 2 CYCLOPENTEN L ONES). 1989, NO. 7, 477 92. SYNTHESISa
  164482. GABRIEL WEATHERHEAD
  164483. 10303N
  164484. 2/28/96
  164485. A REVIEW. JENKS, W. S.; TURRO, N. J. EXCHANGE EFFECTS AND CIDEP (CHEMICALLY INDUCED DYNAMIC ELECTRON POLARIZATION). 1990, 13(3), 237 300. RESEARCH ON CHEMICAL INTERMEDIATESa
  164486. GABRIEL WEATHERHEAD
  164487. 10304N
  164488. 2/28/96V
  164489. A REVIEW. EISCH, JOHN J.; SEXSMITH, STEPHEN R. INTERMEDIATES AND REACTION MECHANISMS IN THE INTERACTION OF NICKEL(0) COMPLEXES WITH ORGANIC SUBSTRATES. 1990,13(2),149 192. RESEARCH ON CHEMICAL INTERMEDIATESa
  164490. GABRIEL WEATHERHEAD
  164491. 10305N
  164492. 2/28/96V
  164493. A REVIEW. LEUENBERGER, H. G. W. INTERRELATIONS OF CHEMISTRY AND BIOTECHNOLOGY. 1. BIOTRANSFORMATION
  164494. A USEFUL TOOL IN ORGANIC CHEMISTRY. 1990, 62(4), 753 68. PURE AND APPLIED CHEMISTRYa
  164495. GABRIEL WEATHERHEAD
  164496. 10306N
  164497. 2/28/96V
  164498. A REVIEW. MANSUY, D. BIOMIMETIC CATALYSTS FOR SELECTIVE OXIDATION IN ORGANIC CHEMISTRY. 1990, 62(4), 741 6. PURE AND APPLIED CHEMISTRYa
  164499. GABRIEL WEATHERHEAD
  164500. 10307N
  164501. 2/28/96
  164502. A REVIEW. WANG, XIU CHUN, WONG, HENRY N. C. THE CHEMISTRY OF CYCLOOCTA[2,1 B:3,4 B]DIPYRIDINE AND ITS DERIVATIVES. 1990, 62(3), 565 8. PURE AND APPLIED CHEMISTRYa
  164503. GABRIEL WEATHERHEAD
  164504. 10308N
  164505. 2/28/96V
  164506. A REVIEW. HAFNER, KLAUS. NOVEL PENTAFULVENES
  164507. VERSATILE BUILDING BLOCKS IN P PERIMETER CHEMISTRY. 1990, 62(3), 531 40. PURE AND APPLIED CHEMISTRYa
  164508. GABRIEL WEATHERHEAD
  164509. 10309N
  164510. 2/28/96V
  164511. A REVIEW. GARRATT, PETER J.; PAYNE, DAVID  TSOTINIS, ANDREW. BATTERED BENZENE AND TWISTED ETHENE. 1990, 62(3), 525 30. PURE AND APPLIED CHEMISTRYa
  164512. GABRIEL WEATHERHEAD
  164513. 10310N
  164514. 2/28/96V
  164515. A REVIEW. ASHE, A. J. III, DRONE F. J., KAUSCH, C. M., KROKER, J. AL, TAWEEL, S. M. BOREPINS AND GROUP 15 ELEMENT HETEROLES. 1990, 62(3), 513 17. PURE AND APPLIED CHEMISTRYa
  164516. GABRIEL WEATHERHEAD
  164517. 10311N
  164518. 2/28/96VqA REVIEW. SUTHERLAND, IAN 0. CYCLOPHANES AS SYNTHETIC RECEPTORS. 1990, 62(3), 499 504. PURE AND APPLIED CHEMISTRY
  164519. GABRIEL WEATHERHEAD
  164520. 10312N
  164521. 2/28/96V
  164522. A REVIEW. GUTSCHE, C. DAVID; ROGERS, JANET S.; STEWART, DONALD; SEE, KEAT AUN. CALIXARENES: PARADOXES AND PARADIGMS IN MOLECULAR BASKETS. 1990, 62(3), 485 91. PURE AND APPLIED CHEMISTRYa
  164523. GABRIEL WEATHERHEAD
  164524. 10313N
  164525. 2/28/96VwA REVIEW. TODA, FUMIO. A MODERN ASPECT OF CLASSICAL AROMATIC COMPOUNDS. 1990, 62(3), 417 22. PURE AND APPLIED CHEMISTRYa
  164526. GABRIEL WEATHERHEAD
  164527. 10314N
  164528. 2/28/96VuA REVIEW. KROTO, HAROLD. C60, FULLERENES, GIANT FULLERENES, AND SOOT. 1990, 62(3), 407 15. PURE AND APPLIED CHEMISTRYa
  164529. GABRIEL WEATHERHEAD
  164530. 10315N
  164531. 2/28/96V
  164532. A REVIEW. HUENIG SIEGFRIED. AROMATIC/QUINOID SYSTEMS: PRINCIPLES AND APPLICATIONS. 1990, 62(3), 395 406. PURE AND APPLIED CHEMISTRYa
  164533. GABRIEL WEATHERHEAD
  164534. 10316N
  164535. 2/28/96
  164536. A REVIEW. BOCK, HANS. NOVEL MAIN GROUP ELEMENT CYCLIC MOLECULES AND THEIR RADICAL IONS: ARE THEY AROMATIC? 1990, 62(3), 383 94. PURE AND APPLIED CHEMISTRYa
  164537. GABRIEL WEATHERHEAD
  164538. 10317N
  164539. 2/28/96V
  164540. A REVIEW. YAMAGUCHI, MASAO; MIYAZAWA, TAKEO; TAKATA, TOSHIKAZU; ENDO, TAKESHI. APPLICATION OF REDOX SYSTEM BASED ON NITROXIDES TO ORGANIC SYNTHESIS. 1990, 62(2), 217 22. PURE AND APPLIED CHEMISTRYa
  164541. GABRIEL WEATHERHEAD
  164542. 10318N
  164543. 2/28/96VwA REVIEW. HIDEG, KALMAN. NOVEL, POTENTIALLY USEFUL SPIN LABEL REAGENTS. 1990, 62(2), 207 12. PURE AND APPLIED CHEMISTRYa
  164544. GABRIEL WEATHERHEAD
  164545. 10319N
  164546. 2/28/96V
  164547. A REVIEW. PERKINS, M. JOHN; BERTI, CORRADO; BROOKS, DEBORAH J.; GRIERSON, LEBERT, GRIMES, JEAN A. M.; JENKINS, TERENCE C. SMITH, SUSAN L. ACYL NITROXIDES: REACTIONS AND REACTIVITY. 1990, 62(2), 195 200. PURE AND APPLIED CHEMISTRYa
  164548. GABRIEL WEATHERHEAD
  164549. 10320N
  164550. 2/28/96
  164551. VbA REVIEW. JIANG, XIKUI. POLYFLUORINATED NITROXIDES. 1990, 62(2), 189 94 PURE AND APPLIED CHEMISTRYa
  164552. GABRIEL WEATHERHEAD
  164553. 10321N
  164554. 2/28/96VqA REVIEW. AURICH, HANS GUENTER. THE CHEMISTRY OF VINYL NITROXIDES. 1990, 62(2), 183 8. PURE AND APPLIED CHEMISTRYa
  164555. GABRIEL WEATHERHEAD
  164556. 10322N
  164557. 2/28/96V|A REVIEW. VOLODARSKII, L. B. ADVANCES IN THE CHEMISTRY OF STABLE NITROXIDES. 1990, 62(2), 177 81. PURE AND APPLIED CHEMISTRYa
  164558. GABRIEL WEATHERHEAD
  164559. 10323N
  164560. 2/28/96V
  164561. A REVIEW. BARONE, GUIDO; GIANCOLA, CONCETTA. PEPTIDE PEPTIDE INTERACTIONS IN WATER AND CONCENTRATED UREA SOLUTIONS. 1990, 62(1), 57 68. PURE AND APPLIED CHEMISTRYa
  164562. GABRIEL WEATHERHEAD
  164563. 10324N
  164564. 2/28/96V
  164565. A REVIEW. GILDAY, JOHN P.; PAQUETTE, LEO A. CARBON CARBON BOND CLEAVAGE BY THE HALLER BAUER AND RELATED REACTIONS. 1990, 22(2), 167 201. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  164566. GABRIEL WEATHERHEAD
  164567. 10325N
  164568. 2/28/96
  164569. A REVIEW. CHOU, TA SHUE, TSO, HSI HWA. USE OF SUBSTITUTED 3 SULFOLENES AS PRECURSORS FOR 1,3 BUTADIENES. 1989, 21(3), 257 96. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  164570. GABRIEL WEATHERHEAD
  164571. 10326N
  164572. 2/28/96V
  164573. A REVIEW. VOL'PIN, M. E.; AKHREM, I. S.; ORLINKOV, A. V. APROTIC ORGANIC SUPERACIDS
  164574. EFFICIENT REAGENTS AND CATALYSTS FOR TRANSFORMATIONS OF ALKANES AND CYCLOALKANES UNDER MILD CONDITIONS. 1989, 13(10 11), 771 90. NEW JOURNAL OF CHEMISTRYa
  164575. GABRIEL WEATHERHEAD
  164576. 10327N
  164577. 2/28/96V
  164578. A REVIEW. SIEDLE, A. R. SOLID STATE CHEMISTRY OF MOLECULAR METAL OXIDE CLUSTERS. CARBON HYDROGEN ACTIVATION REACTIONS OF AN IRIDIUM POLYOXOMETALLATE. 1989,13(10 11), 719 23. NEW JOURNAL OF CHEMISTRYa
  164579. GABRIEL WEATHERHEAD
  164580. 10328N
  164581. 2/28/96V
  164582. A REVIEW. KHENKIN, A. M.; SHILOV, A. E. BIOMIMETIC ALKANE OXIDATION IN THE PRESENCE OF IRON COMPLEXES. 1989,13(10 11), 669 67. NEW JOURNAL OF CHEMISTRYa
  164583. GABRIEL WEATHERHEAD
  164584. 10329N
  164585. 2/28/96VjA REVIEW. WEILL, RAYNAL J. LITTLE STORY OF GREAT SYNTHESES. 1989, 13(8 9), 569 74 NEW JOURNAL OF CHEMISTRYa
  164586. GABRIEL WEATHERHEAD
  164587. 10330N
  164588. 2/28/96V
  164589. A REVIEW. YAMANAKA, HIROSHI, SAKAMOTO, TAKAO; NIITSUMA, SETSUKO. PYRIMIDINE N OXIDES: SYNTHESIS, STRUCTURES, AND CHEMICAL PROPERTIES. 1990, 31(5), 923. HETEROCYCLESa
  164590. GABRIEL WEATHERHEAD
  164591. 10331N
  164592. 2/28/96V
  164593. A REVIEW. FILLOL, LUIS; MIRANDA, MIGUEL A.; MORERA, ISABEL M. SHEIKH, HAMID. PHOTOCHEMISTRY OF 2(3H)  AND 2(5H)FURANONES. 1990, 31(4), 751. HETEROCYCLESa
  164594. GABRIEL WEATHERHEAD
  164595. 10332N
  164596. 2/28/96VaA REVIEW. FREEMAN, FILLMORE. THE CHEMISTRY OF 4H 1,3 DITHIINS. 1990, 31(4), 701 750. HETEROCYCLESa
  164597. GABRIEL WEATHERHEAD
  164598. 10333N
  164599. 2/28/96V
  164600. A REVIEW. ZAKREWSKI, JANUSZ. REACTIONS OF THE ETA5 PYRROLYL LIGAND: A NEW CHALLENGE IN THE CHEMISTRY OF PYRROLES. 1990, 31(2), 383 396. HETEROCYCLESa
  164601. GABRIEL WEATHERHEAD
  164602. 10334N
  164603. 2/28/96
  164604. A REVIEW. MARAMATSU, TAKASHI; IKEGAMI, YUSAKU; HANAYA, KAORU. THE THERMAL AND PHOTOCHEMICNL BEHAVIORS OF THE CYCLOMERS OF ETHYLENEBIS  AND TRIMETHYLENEBIS(PYRIDINYL) DIRADICALS. 1990, 30(SPECIAL ISSUE NO. 2),1307 1318. HETEROCYCLESa
  164605. GABRIEL WEATHERHEAD
  164606. 10335N
  164607. 2/28/96V
  164608. A REVIEW. NOZOE, TETSUO. CYCLOHEPTA[B][1,4]BENZOXAZINE AND ITS RELATED COMPOUNDS. SOME NOVEL ASPECTS IN HETEROCYCLIC CHEMISTRY. 1990, 30(SPECIAL ISSUE NO. 2), 1263 1306. HETEROCYCLESa
  164609. GABRIEL WEATHERHEAD
  164610. 10336N
  164611. 2/28/96V
  164612. A REVIEW. DAI, WEI MIN; NAGAO, YOSHIMITSU; FUJITA, EIICHI. RECENT PROGRESS IN ASYMMETRIC SYNTHESIS OF PYRROLIZIDINES. 1990, 30(SPECIAL ISSUE NO. 2),1231 1262. HETEROCYCLESa
  164613. GABRIEL WEATHERHEAD
  164614. 10337N
  164615. 2/28/96V
  164616. A REVIEW. KLEMM, LEROY H. INTERRELATIONSHIPS AMONG PERI CONDENSED THIOPHENES AND SOME POLYCYCLIC AROMATIC COMPOUNDS. 1990, 30(SPECIAL ISSUE NO. 2),1195 1218. HETEROCYCLESa
  164617. GABRIEL WEATHERHEAD
  164618. 10338
  164619. 2/28/96V
  164620. A REVIEW. OKUDA, TAKUO; YOSHIDA, TAKASHI, HATANO, TSUTOMU. OLIGOMERIC HYDROLYZABLE TANNINS, A NEW CLASS OF PLANT POLYPHENOLS. 1990, 30(SPECIAL ISSUE NO. 2),1195 1218. HETEROCYCLESa
  164621. GABRIEL WEATHERHEAD
  164622. 10339N
  164623. 2/28/96V
  164624. A REVIEW. UNDHEIM, KJELL, BENNECHE, TORE. METALLATION AND METAL ASSISTED BOND FORMATION IN P ELECTRON DEFICIENT HETEROCYCLES. 1990, 30(SPECIAL ISSUE NO. 2),1155 1193. HETEROCYCLESa
  164625. GABRIEL WEATHERHEAD
  164626. 10340N
  164627. 2/28/96V
  164628. A REVIEW. KANEMASA, SHUJI; TSUGE, OTOHIKO. RECENT ADVANCES IN SYNTHETIC APPLICATIONS OF NITRILE OXIDE CYCLOADDITION (1981 1989). 1990, 30(SPECIAL ISSUE NO. 1), 719 736. HETEROCYCLESa
  164629. GABRIEL WEATHERHEAD
  164630. 10341N
  164631. 2/28/96VyA REVIEW. REBEK, JULIUS, JR. HETEROCYCLES AND MOLECULAR RECOGNITION. 1990, 30(SPECIAL ISSUE NO. 1), 707 717. HETEROCYCLESa
  164632. GABRIEL WEATHERHEAD
  164633. 10342N
  164634. 2/28/96
  164635. A REVIEW. MCDANIEL, CHRISTOPHER W.; BRADSHAW, JERALD S.; IZATT, REED M. PROTON IONIZABLE CROWN ETHERS. A SHORT REVIEW. 1990, 30(SPECIAL ISSUE NO. 1), 665 706. HETEROCYCLESa
  164636. GABRIEL WEATHERHEAD
  164637. 10343N
  164638. 2/28/96VwA REVIEW. BROWN, MARK J. LITERATURE REVIEW OF THE ESTER ENOLATE IMINE CONDENSATION. 1989, 29(11), 2225 44. HETEROCYCLESa
  164639. GABRIEL WEATHERHEAD
  164640. 10344N
  164641. 2/28/96VeA REVIEW. KADABA, PANKAJA, K. 1,2,4 TRIAZOLINES. 1989, 46,169 281. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164642. GABRIEL WEATHERHEAD
  164643. 10345N
  164644. 2/28/96V
  164645. A REVIEW. TERASHIMA, MASANAO; ISHIKURA MINORU. BORON SUBSTITUTED HETEROAROMATIC COMPOUNDS. 1989, 46, 143 67. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164646. GABRIEL WEATHERHEAD
  164647. 10346N
  164648. 2/28/96
  164649. A REVIEW. CHARUSHIN, V. N.; ALEKSEEV, S. G.; CHUPAKHIN, 0. N.; VAN DER PLAS, H. C. BEHAVIOR OF MONOCYCLIC 1,2,4 TRIAZINES IN REACTIONS WITH C , N , O , AND S NUCLEOPHILES. 1989, 46, 73 142. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164650. GABRIEL WEATHERHEAD
  164651. 10347N
  164652. 2/28/96VaA REVIEW. PERLMUTTER, HOWARD D. 1,5 DIAZOCINES. 1989, 46,1 72. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  164653. GABRIEL WEATHERHEAD
  164654. 10348N
  164655. 2/28/96V
  164656. A REVIEW. DAVES, G. DOYLE, JR. C GLYCOSIDE SYNTHESIS BY PALLADIUM MEDIATED GLYCAL AGLYCON COUPLING REACTIONS. 1990, 23(6), A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164657. GABRIEL WEATHERHEAD
  164658. 10349N
  164659. 2/28/96V
  164660. A REVIEW. ADAM, WALDEMAR; GRABOWSKI, SVEN; WILSON, R. MARSHALL. LOCALIZED CYCLIC TRIPLET DIRADICALS. LIFETIME DETERMINATION BY TRAPPING WITH OXYGEN. 1990, 23(5),165 72. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  164661. GABRIEL WEATHERHEAD
  164662. 10350N
  164663. 2/28/96
  164664. A REVIEW. ADDITION REACTION OF EPOXY COMPOUNDS WITH ESTERS AND ITS APPLICATION FOR POLYMER SYNTHESIS. NISHIKUBO T.PP. 218 33 J. SYN. ORG. CHEM. JPN. 49(3), 1991a
  164665. GABRIEL WEATHERHEAD
  164666. 10351N
  164667. 2/28/96V{A REVIEW. THE CHEMISTRY OF L HYDROXYINDOLES AND THEIR DERIVATIVES. SOMEI M., PP. 205 17 J. SYN. ORG. CHEM. JPN. 49(3), 1991a
  164668. GABRIEL WEATHERHEAD
  164669. 10352N
  164670. 2/28/96V
  164671. A REVIEW. RECENT PROGESS IN MANUFACTURING TECHNOLOGY FOR AROMATIC ALDEHYDES. MAKI T YOKOYAMA T., PP. 195 204 J. SYN. ORG. CHEM. JPN. 49(3), 1991a
  164672. GABRIEL WEATHERHEAD
  164673. 10353N
  164674. 2/28/96VrA REVIEW. METALATION REACTIONS OF ISOCYANIDES. ITO Y., MURAKAMI M., PP. 184 94 J. SYN. ORG. CHEM. JPN. 49(3), 1991a
  164675. GABRIEL WEATHERHEAD
  164676. 10354N
  164677. 2/28/96V
  164678. A REVIEW. SYNTHETIC TRANSFORMATIONS USING ARENESULFONYLOXY GROUPS, FIRST AS ELECTROPHILES, THEN AS LEAVING GROUPS. HOFFMAN R. V., PP. 1109 35 TETRAHEDRON 47(7), 1991a
  164679. GABRIEL WEATHERHEAD
  164680. 10355N
  164681. 2/28/96V
  164682. A REVIEW. FOUR MEMBERED CYCLIC NITRONES   SYNTHESIS AND REACTIVITY. VERBOOM W., REINHOUDT D. N., PP. 704 13 BULL. SOC. CHIM. FRANCE (6), 1990a
  164683. GABRIEL WEATHERHEAD
  164684. 10356N
  164685. 2/28/96V
  164686. A REVIEW. RECENT ADVANCES IN THE FIELD OF HETEROSUBSTITUTED CARBENIUM IONS   A SURVEY. HEVESI L., PP. 697 703 BULL. SOC. CHIM. FRANCE (6), 1990a
  164687. GABRIEL WEATHERHEAD
  164688. 10357N
  164689. 2/28/96V
  164690. A REVIEW. TRANSFORMATIONS OF BETA HYDROXYALKYL SELENIDES TO ALDEHYDES AND KETONES. KRIEF A. LABOUREUR J. L., DUMONT W., LABAR D., PP. 681 96 BULL. SOC. CHIM. FRANCE (6), 1990a
  164691. GABRIEL WEATHERHEAD
  164692. 10358N
  164693. 2/28/96V
  164694. A REVIEW. A SURVEY OF THE RADICAL MEDIATED CYCLIZATION OF ALPHA HALOACETALS OF CYCLIC ALLYL ALCOHOLS AS A GENERAL ROUTE TO THE CONTROL OF VICINAL REGIO  AND STEREOCHEMISTRY. STORK G.. PP. 675  80 BULL. SOC. CHIM. FRANCE (6), 1990a
  164695. GABRIEL WEATHERHEAD
  164696. 10359N
  164697. 2/28/96
  164698. VmA REVIEW. METHODS FOR THE SYNTHESIS OF ALLYLSILANES. 1. SARKAR T.K, PP. 969 83 SYNTHESIS STUTTGART (11), 1990a
  164699. GABRIEL WEATHERHEAD
  164700. 10360N
  164701. 2/28/96VvA REVIEW. EXPANDING INDUSTRIAL APPLICATIONS OF PALLADIUM CATALYSTS. TSUJI J., PP. 739 49 SYNTHESIS STUTTGART (9), 1990a
  164702. GABRIEL WEATHERHEAD
  164703. 10361N
  164704. 2/28/96V
  164705. A REVIEW. REACTIONS OF GROUP LVB ORGANOBIMETALLIC COMPOUNDS WITH ELECTROPHILIC REAGENTS. BOBROVSKII S. I., BUNDEL Y. G., PP. 121 66 J. ORGANOMETAL. CHEM. 395(2), 1990a
  164706. GABRIEL WEATHERHEAD
  164707. 10362N
  164708. 2/28/96V
  164709. A REVIEW. AT THE CROSSROADS OF CHEMISTRY AND IMMUNOLOGY   CATALYTIC ANTIBODIES. LERNER R. A., BENKOVIC S. J., SCHULTZ P. G., PP. 659 67 SCIENCE 252(5006), 1991a
  164710. GABRIEL WEATHERHEAD
  164711. 10363N
  164712. 2/28/96V
  164713. A REVIEW. CONTROLLING ELECTROCHEMICAL CATALYSIS WITH SURFACTANT MICROSTRUCTURES. RUSLING J. F., PP. 75 81 ACCOUNT CHEM. RES. 24(3), 1991a
  164714. GABRIEL WEATHERHEAD
  164715. 10364
  164716. 2/28/96V
  164717. A REVIEW. PREPARATION AND REACTIONS OF ORGANORUTHENIUM(LV) COMPLEXES. ITOH K., NAGASHIMA H., FUKAHON T., PP. 177 86 NIPPON KAGAKU KAISHI (3), 1991a
  164718. GABRIEL WEATHERHEAD
  164719. 10365N
  164720. 2/28/96V
  164721. A REVIEW. ETHER LIPIDS   SYNTHESIS AND APPLICATION IN TUMOR THERAPY. ZEISIG R., ARNDT D., BRACHWITZ H., PP. 809 18 PHARMAZIE 45(11), 1990a
  164722. GABRIEL WEATHERHEAD
  164723. 10366N
  164724. 2/28/96VtA REVIEW. NEW METHODS FOR THE SYNTHESIS OF TROPONOID COMPOUNDS. BANWELL M. G., PP. 1 36 . AUST. J. CHEM. 44(1), 1991a
  164725. GABRIEL WEATHERHEAD
  164726. 10367N
  164727. 2/28/96V
  164728. A REVIEW. RECENT PROGRESS IN THE SYNTHESIS AND REACTIVITY OF NITROKETONES. ROSINI G., BALLINI R., PETRINI M.. MAROTTA E., RIGHI P., PP. 707 46 ORG. PREP. PROCEDURE INT. 22(6), 1990a
  164729. GABRIEL WEATHERHEAD
  164730. 10368N
  164731. 2/28/96
  164732. A REVIEW. ARGININE, HISTIDINE AND TRYTOPHAN IN PEPTIDE SYNTHESIS   THE INDOLE FUNCTION OF TRYPTOPHAN. RZESZOTARSKA B., MASIUKIEWICZ E.. PP. 655 706 ORG. PREP. PROCEDURE INT. 22(6), 1990a
  164733. GABRIEL WEATHERHEAD
  164734. 10369N
  164735. 2/28/96V
  164736. A REVIEW. ARGININE, HISTIDINE AND TRYTOPHAN IN PEPTIDE SYNTHESIS   THE INDOLE FUNCTION OF TRYPTOPHAN. RZESZOTARSKA B., MASIUKIEWICZ E.. PP. 655 706a
  164737. GABRIEL WEATHERHEAD
  164738. 10370N
  164739. 2/28/96V
  164740. A REVIEW. THE SYNTHESIS OF DITHIOLENE DYES WITH STRONG NEAR IR ABSORPTION. MUELLER VESTERHOFF U. T., VANCE B.. YOON D. 1., PP. 909 32 TETRAHEDRON 47(6), 1991a
  164741. GABRIEL WEATHERHEAD
  164742. 10371N
  164743. 2/28/96V|A REVIEW. BAKERS YEAST MEDIATED TRANSFORMATION IN ORGANIC CHEMISTRY. CSUK R., GLANZER B. 1., PP 49 97 CHEM. REV. 91(1), 1991a
  164744. GABRIEL WEATHERHEAD
  164745. 10372N
  164746. 2/28/96V
  164747. A REVIEW. CHEMISTRY OF THE POLYHEDRAL BORON HALIDES AND THE DIBORON TETRAHALIDES. MORRISON J. A., PP. 35 48 CHEM. REV. 91(1), 1991
  164748. GABRIEL WEATHERHEAD
  164749. 10373N
  164750. 2/28/96VvA REVIEW. ISOTHIOCYANATES IN THE CHEMISTRY OF HETEROCYCLES. MUKERJEE A. K., ASHARE R., PP. 1 24 CHEM. REV. 91(1), 1991a
  164751. GABRIEL WEATHERHEAD
  164752. 10374N
  164753. 2/28/96V
  164754. A REVIEW. SOME NOVEL LON MOLECULE CHEMISTRY WITHIN VANDERWAALS CLUSTERS. GARVEY J. F., PEIFER W. R., COOLBAUGH M. T., PP. 48 54 ACCOUNT CHEM. RES. 24(2), 1991a
  164755. GABRIEL WEATHERHEAD
  164756. 10375N
  164757. 2/28/96V
  164758. A REVIEW. USE OF PREASSEMBLED FE/S AND FE/MO/SI CLUSTERS IN THE STEPWISE SYNTHESIS OF POTENTIAL ANALOGS FOR THE FE/MOLS SITE IN NITROGENASE. COUCOUVANIS D., PP. 1 8 ACCOUNT CHEM. RES. 24(1), 1991a
  164759. GABRIEL WEATHERHEAD
  164760. 10376N
  164761. 2/28/96V
  164762. A REVIEW. CHEMICAL AND BIOCHEMICAL STUDIES ON REACTIVITIES, FORMATIONS AND TOXICITIES OF REACTIVE OXYXEN SPECIES. NAGANO T., PP. 103 19 YAKUGAKU ZASSHI J. PHARM. SOC. J. 111(2), 1991a
  164763. GABRIEL WEATHERHEAD
  164764. 10377N
  164765. 2/28/96
  164766. A REVIEW. STUDIES ON OXACEPHEMS, AN ARTIFCIAL TYPE OF BETA LACTAM ANTIBIOTICS. NAGATA W., NARTSADA M., YOSHIOKA M., YOSHIDA T.. ONOUE H.. PP. 77 102 IN JAPANESE. YAKUGAKU ZASSHI J. PHARM. SOC. J. 111(2), 1991a
  164767. GABRIEL WEATHERHEAD
  164768. 10378N
  164769. 2/28/96V
  164770. A REVIEW. RECENT ADVANCES ON THE ENZYMATIC DEGRADATION OF LIGNIN. LABAT G.; MEUNIER B., PP. 553 64  BULL. SOC. CHIM. FRANCE (4), 1990a
  164771. GABRIEL WEATHERHEAD
  164772. 10379N
  164773. 2/28/96V
  164774. A REVIEW. BICYCLO(4.2.1)NONANE SKELETON   CONFORMATIONAL ANALYSIS, SYNTHESIS, REACTIVITY. CASANOVA J., KOUKOUA G., WAEGELL B., PP. 528 52 BULL. SOC. CHIM. FRANCE (4), 1990a
  164775. GABRIEL WEATHERHEAD
  164776. 10380N
  164777. 2/28/96V
  164778. A REVIEW. STABLE ISOTOPICALLY ENRICHED D GLUCOSE   STRATEGIES TO INTRODUCE CARBON, HYDROGEN AND OXYGEN ISOTOPES AT VARIOUS SITES. SENANNI A. S., VUORINEN T., BONDO P. B., PP. 513 41  J. CARBOHYD. CHEM. 9(5), 1990a
  164779. GABRIEL WEATHERHEAD
  164780. 10381N
  164781. 2/28/96
  164782. A REVIEW. SYNTHETIC PROCEDURES FOR THE PREPARATION OF DEUTERIUM LABELED ANALOGS OF NATURALLY OCCURRING STEROIDS. WUDY S. A., PP. 463 71  STEROIDS 55(10) 1990a
  164783. GABRIEL WEATHERHEAD
  164784. 10382N
  164785. 2/28/96VuA REVIEW. SYNTHESIS OF C 13 1ABELED STEROID HORMONES. ZOMER G., SLAVENUITER J. F. C., PP. 440 2  STEROIDS 55(10) 1990a
  164786. GABRIEL WEATHERHEAD
  164787. 10383N
  164788. 2/28/96V
  164789. A REVIEW. TELRAZOLIUM SULTS. ZHIVICH A.; KOLDOBSKII, G. I.; OSTROVSKII, V. A. 1587 99 KHIM. GETEROTSIKL. SOEDIN. SSSR (12), 1990a
  164790. GABRIEL WEATHERHEAD
  164791. 10384N
  164792. 2/28/96VcA REVIEW. WILMAN, DERRY E. V., ED. THE CHEMISTRY OF ANTITUMOR AGENTS. BLACKIE: GLASGOW, U.K., 1990.a
  164793. GABRIEL WEATHERHEAD
  164794. 10385N
  164795. 2/28/96V
  164796. A REVIEW. TROGLER, WILLIAM C., ED. ORGANOMETALLIC RADICAL PROCESSES (JOURNAL OF ORGANOMETALLIC CHEMISTRY LIBRARY, VOL. 22). ELSEVIER: AMSTERDAM, 1990.a
  164797. GABRIEL WEATHERHEAD
  164798. 10386N
  164799. 2/28/96
  164800. A REVIEW. SMITH, JANICE G.; FIESER, MARY. FIESER AND FIESER'S REAGENTS FOR ORGANIC SYNTHESIS: COLLECTIVE INDEX FOR VOLUMES 1 12. WILEY: NEW YORK, 1990.a
  164801. GABRIEL WEATHERHEAD
  164802. 10387N
  164803. 2/28/96V
  164804. A REVIEW. SEYMOUR, RAYMOND, B.; CARRAHER, CHARLES E. GIANT MOLECULES. ESSENTIAL MATERIALS FOR EVERYDAY LIVING AND PROBLEM SOLVING. WILEY: NEW YORK, 1990.a
  164805. GABRIEL WEATHERHEAD
  164806. 10388N
  164807. 2/28/96V
  164808. A REVIEW. SERRATOSA, FELIX. ORGANIC CHEMISTRY IN ACTION. THE DESIGN OF ORGANIC SYNTHESIS (STUDIES IN ORGANIC CHEMISTRY, VOL. 41). ELSEVIER: AMSTERDAM, 1990.a
  164809. GABRIEL WEATHERHEAD
  164810. 10389N
  164811. 2/28/96V
  164812. A REVIEW. SANDLER, STANLEY R.; KARO, WOLF. ORGANIC FUNCTIONAL GROUP PREPARATIONS, 2ND ED., VOL. III (ORGANIC CHEMISTRY, A SERIES OF MONOGRAPHS, VOL. 12, PT. 3). ACADEMIC PRESS: SAN DIEGO, CA, 1989.a
  164813. GABRIEL WEATHERHEAD
  164814. 10390N
  164815. 2/28/96
  164816. A REVIEW. PATAI, SAUL, ED. THE CHEMISTRY OF SULPHINIC ACIDS ESTERS, AND THEIR DERIVATIVES (THE CHEMISTRY OF FUNCTIONAI GROUPS). WILEY: CHICHESTER, U.K., 1990.a
  164817. GABRIEL WEATHERHEAD
  164818. 10391N
  164819. 2/28/96V
  164820. A REVIEW. PATAI, SAUL, ED. THE CHEMISTRY OF SULPHENIC ACIDS AND THEIR DERIVATIVES (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1990.a
  164821. GABRIEL WEATHERHEAD
  164822. 10392N
  164823. 2/28/96V
  164824. A REVIEW. PATAI, SAUL, ED. THE CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, VOL. 2, PARTS 1 AND 2 (THE CHEMISTRY OF FUNCTIONAL GROUPS: SUPPLEMENT A). WILEY: CHICHESTER U.K., 1989.a
  164825. GABRIEL WEATHERHEAD
  164826. 10393N
  164827. 2/28/96VIA REVIEW. OLAH, GEORGE, A., ED. CAGE HYDROCARBONS. WILEY: NEW YORK, 1990.a
  164828. GABRIEL WEATHERHEAD
  164829. 10394N
  164830. 2/28/96V^A REVIEW. NINOMIYA, 1.; NAITO, T., EDS. PHOTOCHEMICAL SYNTHESIS. ACADEMIC PRESS: LONDON, 1989.a
  164831. GABRIEL WEATHERHEAD
  164832. 10395N
  164833. 2/28/96
  164834. A REVIEW. MUKAYIAMA, TERUAKI. CHALLENGES IN SYNTHETIC ORGANIC CHEMISTRY (BALDWIN, J. E., TRANSLATION ED.). CLARENDON PRESS: OXFORD, U.K., 1990.a
  164835. GABRIEL WEATHERHEAD
  164836. 10396N
  164837. 2/28/96VwA REVIEW. MICHL, JOSEPH; BONACIC KOUTECKY, VLASTA. ELECTRONIC ASPECTS OF ORGANIC PHOTOCHEMISTRY. WILEY: NEW YORK, 1990.a
  164838. GABRIEL WEATHERHEAD
  164839. 10397N
  164840. 2/28/96V
  164841. A REVIEW. LUKEVICS, E., PUDOVA, 0.; STURKOVICH, R. MOLECULAR STRUCTURE OF ORGANOSILICON COMPOUNDS (TRANSLATED BY EIDUSS, J.; AVERTSEV, S.). ELLIS HORWOOD: CHICHESTER, U.K., 1989.a
  164842. GABRIEL WEATHERHEAD
  164843. 10398N
  164844. 2/28/96V
  164845. A REVIEW. LEY, STEVE V., LOW, CAROLINE M. R. ULTRASOUND IN SYNTHESIS (REACTIVITY AND STRUCTURE CONCEPTS IN ORGANIC CHEMISTRY, VOL. 27), SPRINGER VERLAG: BERLIN, 1989.a
  164846. GABRIEL WEATHERHEAD
  164847. 10399N
  164848. 2/28/96V
  164849. A REVIEW. LEDNICER, DANIEL; MITSCHER, LESTER A.; GEORG, GUNDA 1.EDS. THE ORGANIC CHEMISTRY OF DRUG SYNTHESIS, VOL. 4. WILEY: NEW YORK, 1990.
  164850. GABRIEL WEATHERHEAD
  164851. 10400N
  164852. 2/28/96VXA REVIEW. LAROCK, RICHARD C. COMPREHENSIVE ORGANIC TRANSFORMATIONS. VCH: NEW YORK, 1989.a
  164853. GABRIEL WEATHERHEAD
  164854. 10401N
  164855. 2/28/96V
  164856. A REVIEW. KATRITZKY, ALAN R.; TAYLOR, ROGER. ELECTROPHILIC SUBSTITUTION OF HETEROCYCLES: QUANTITATIVE ASPECTS (ADVANCES IN HETEROCYCLIC CHEMISTRY, VOL. 47). ACADEMIC PRESS: SAN DIEGO, CA, 1990.a
  164857. GABRIEL WEATHERHEAD
  164858. 10402N
  164859. 2/28/96VtA REVIEW. HUDLICKY, MILOS. OXIDATIONS IN ORGANIC CHEMISTRY (ACS MONOGRAPH L86). AMERICANCHEMICALSOCIETY: WASHINGTON,a
  164860. GABRIEL WEATHERHEAD
  164861. 10403N
  164862. 2/28/96V
  164863. A REVIEW. HAUFE, GUNTER, MAUN, GERHARD. CHEMISTRY OF ALICYCLIC COMPOUNDS: STRUCTURE AND CHEMICAL TRANSFORMATIONS (STUDIES IN ORGANIC CHEMISTRY, VOL. 38). ELSEVIER: AMSTERDAM, 1989.a
  164864. GABRIEL WEATHERHEAD
  164865. 10404N
  164866. 2/28/96
  164867. (V{A REVIEW. GUTMAN, IVAN; CYVIN, SVEN J. INTRODUCTION TO THE THEORY OF BENZENOID HYDROCARBONS. SPRINGER VERLAG: BERLIN, 1989.a
  164868. GABRIEL WEATHERHEAD
  164869. 10405N
  164870. 2/28/96V
  164871. A REVIEW. GRANT, DAVID, J. W., HIGUCHI, TAKERU. SOLUBILITY BEHAVIOR OF ORGANIC COMPOUNDS (TECHNIQUES OF CHEMISTRY, VOL. 21). WILEY: NEW YORK, 1990.a
  164872. GABRIEL WEATHERHEAD
  164873. 10406N
  164874. 2/28/96VsA REVIEW. GIELEN, MARCEL, ED. TOPICS IN PHYSICAL ORGANOMETALLIC CHEMISTRY, VOL. 3. FREUND PUBLISHING HOUSE: LONDON,a
  164875. GABRIEL WEATHERHEAD
  164876. 10407N
  164877. 2/28/96VxA REVIEW. GIELEN, MARCEL, ED. TOPICS IN PHYSICAL ORGANOMETALLIC CHEMISTRY, VOL. 2. FREUND PUBLISHING HOUSE: LONDON 1988.a
  164878. GABRIEL WEATHERHEAD
  164879. 10408N
  164880. 2/28/96VkA REVIEW. FRINGUELLI, FRANCESCO; TATICCHI, ALDO. DIENES IN THE DIELS ALDER REACTION. WILEY: NEW YORK, 1990.a
  164881. GABRIEL WEATHERHEAD
  164882. 10409N
  164883. 2/28/96
  164884. A REVIEW. DAVIES, H. G.; GREEN, R. H.; KELLY, D. R., ROBERTS, STANLEY M. BIOTRANSFORMATIONS IN PREPARATIVE ORGANIC CHEMISTRY. THE USE OF ISOLATED ENZYMES AND WHOLE CELL SYSTEMS IN SYNTHESIS. ACADEMIC PRESS: LONDON, 1989.a
  164885. GABRIEL WEATHERHEAD
  164886. 10410N
  164887. 2/28/96V{A REVIEW. CASEY, M., LEONARD, J., LYGO, B., PROCTER, G. ADVANCED PRACTICAL ORGANIC CHEMISTRY. BLACKIE: GLASGOW, U.K., 1990.a
  164888. GABRIEL WEATHERHEAD
  164889. 10411N
  164890. 2/28/96V
  164891. A REVIEW. CAREY, FRANCIS A.; SUNDBERG, RICHARD, J. ADVANCED ORGANIC CHEMISTRY, 3RD EDITION. PART A: STRUCTURE AND MECHANISMS. PART B: REACTIONS AND SYNTHESIS. PLENUM NEW YORK, 1990.a
  164892. GABRIEL WEATHERHEAD
  164893. 10412N
  164894. 2/28/96V
  164895. A REVIEW. BOCHE G., WALBORSKY, H. M. CYCLOPROPANE DERIVED REACTIVE INTERMEDIATES (THE CHEMISTRY OF FUNCTIONAL GROUPS. UPDATES). WILEY: CHICHESTER, U.K., 1990.a
  164896. GABRIEL WEATHERHEAD
  164897. 10413N
  164898. 2/28/96
  164899. A REVIEW. BERNAL, IVAN, ED. STEREOCHEMISTRY OF ORGANOMETALLIC AND INORGANIC COMPOUNDS, VOL. 3: CHEMICAL BONDS
  164900. BETTER WAYS TO MAKE THEM AND BREAK THEM. ELSEVIER: AMSTERDAM, 1989.a
  164901. GABRIEL WEATHERHEAD
  164902. 10414N
  164903. 2/28/96V
  164904. A REVIEW. PETERSON, W. R.; ANDERSON, R.; LARSON, G. L. SILANE BLOCKING AGENTS, P 73. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164905. GABRIEL WEATHERHEAD
  164906. 10415N
  164907. 2/28/96V
  164908. A REVIEW. LAUNER, P. J. INFRARED ANALYSIS OF ORGANOSILICON COMPOUNDS, P 69. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164909. GABRIEL WEATHERHEAD
  164910. 10416N
  164911. 2/28/96V
  164912. A REVIEW. BREY, W. S. SILICON 29 NUCLEAR MAGNETIC RESONANCE, P 60. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164913. GABRIEL WEATHERHEAD
  164914. 10417N
  164915. 2/28/96
  164916. A REVIEW. ARKLES, B. SILANE COUPLING AGENT CHEMISTRY, P 54. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164917. GABRIEL WEATHERHEAD
  164918. 10418N
  164919. 2/28/96V
  164920. A REVIEW. TACKE, R. DRUG DESIGN BY SILA SUBSTITUTION AND MICROBIAL TRANSFORMATIONS OF ORGANOSILICON COMPOUNDS: SOME RECENT RESULTS, P 47. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164921. GABRIEL WEATHERHEAD
  164922. 10419N
  164923. 2/28/96V|A REVIEW. KANNER, B. ORGANOFLUOROSILANES, P 40. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164924. GABRIEL WEATHERHEAD
  164925. 10420N
  164926. 2/28/96V
  164927. A REVIEW. PANNELL, K. H. ORGANOSILICON TRANSITION METAL INTERACTIONS, P 32. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164928. GABRIEL WEATHERHEAD
  164929. 10421N
  164930. 2/28/96
  164931. A REVIEW. FLEMING, I. SILICON MEDIATED STEREOCHEMICALLY CONTROLLED REACTIONS, P 21. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164932. GABRIEL WEATHERHEAD
  164933. 10422N
  164934. 2/28/96V
  164935. A REVIEW. LARSON, G. L. AN INTRODUCTION TO ORGANOSILICON CHEMISTRY, P 9. SILICON COMPOUNDS, REGISTER AND REVIEW, PETRARCH SYSTEMS: BRISTOL, PA, 1987.a
  164936. GABRIEL WEATHERHEAD
  164937. 10423N
  164938. 2/28/96V
  164939. A REVIEW. TISLER, MIHA. SYNTHESES OF HETEROCYCLES BY INTRAMOLECULAR CYCLIZATION OF AMIDINES OR AMIDOXIMES AND IN OUT NITROGEN TRANSLOCATION. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164940. GABRIEL WEATHERHEAD
  164941. 10424N
  164942. 2/28/96V
  164943. A REVIEW. DITTMER, DONALD C. EXPLORATIONS INTO CHALCOGEN HETEROCYCLES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164944. GABRIEL WEATHERHEAD
  164945. 10425N
  164946. 2/28/96
  164947. A REVIEW. YOKOYAMA, MASAHKA; WATANABE, SATOSHI; SUJINO, KEIKO. SYNTHESIS OF HETEROCYCLES DIRECTED TOWARD BIOLOGICAL ACTIVITY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164948. GABRIEL WEATHERHEAD
  164949. 10426N
  164950. 2/28/96V
  164951. A REVIEW. METGNER, PATRICK. THIOCARBONYL COMPOUNDS IN ORGANIC SYNTHESIS: 1,4 ADDITION REACTION OF ENETHIOLATES WITH ENONES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164952. GABRIEL WEATHERHEAD
  164953. 10427N
  164954. 2/28/96V
  164955. A REVIEW. MARKOVSKY, LEONID; PASHINNIK, VALERIJ. FLUOROSULFURANES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164956. GABRIEL WEATHERHEAD
  164957. 10428N
  164958. 2/28/96V
  164959. A REVIEW. OCHIAI,MASIHITO. HYPERVALENTALKYLIODINE(III)CHEMISTRY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164960. GABRIEL WEATHERHEAD
  164961. 10429N
  164962. 2/28/96
  164963. A REVIEW. OAE, SHIGERU, UCHIDA, YUZURU. VALIDITY OF OUR NEW CONCEPT OF LIGAND COUPLING THROUGH HYPERVALENT AND SIMILAR VALENCE SHELL EXPANDED INTERMEDIATES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164964. GABRIEL WEATHERHEAD
  164965. 10430N
  164966. 2/28/96V
  164967. A REVIEW. PETRAGNANI, NICOLA; COMASSETO, JOAO. SELENIUM AND TELLURIUM REAGENTS. PREPARATION AND SYNTHETIC APPLICATIONS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164968. GABRIEL WEATHERHEAD
  164969. 10431N
  164970. 2/28/96V
  164971. A REVIEW. MIKOLAJCZYK, MARIAN. A PHOSPHONATE CARBANIONS: FROM SIMPLE REACTIONS TO THE SYNTHESIS OF CYCLOPENTENONES AND CYCLOPENTANONES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164972. GABRIEL WEATHERHEAD
  164973. 10432N
  164974. 2/28/96
  164975. A REVIEW. HORNER, LEOPOLD. A RETROSPECTIVE VIEW OF THE LOGIC OF CHOICE IN SCIENTIFIC STUDY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 2, SHIGERU OAE, ED., MYU KX.: TOKYO, JAPAN, 1989.a
  164976. GABRIEL WEATHERHEAD
  164977. 10433N
  164978. 2/28/96V
  164979. A REVIEW. STEC, WOJCIECH J. NEW OPPORTUNITIES IN BIOORGANIC PHOSPHORUS CHEMISTRY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  164980. GABRIEL WEATHERHEAD
  164981. 10434N
  164982. 2/28/96
  164983. A REVIEW. REMNUD, G.  ZHOU, X. X., OBERG, B., CHATTOPADHYAYA J. SYNTHESIS AND CONFORMATION OF 2' TO 5' AND 3' TO 5' PHOSPHODIESTER LINKED BRANCHED TRIADENYLATES [A23~I~S A]~ REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.
  164984. GABRIEL WEATHERHEAD
  164985. 10435N
  164986. 2/28/96
  164987. A REVIEW. HATA, TSUJIAKI. A SOLUTION OF THE PROHLEM OF 3' 2' 0 PHOSPHORYL MIGRATION IN OLIGORIBONUCLEOTIDE (RNA) SYNTHESIS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  164988. GABRIEL WEATHERHEAD
  164989. 10436N
  164990. 2/28/96V
  164991. A REVIEW. OAE, SHIGERU. LIGAND COUPLING REACTIONS WITH HYPERVALENT SPECIES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  164992. GABRIEL WEATHERHEAD
  164993. 10437N
  164994. 2/28/96V
  164995. A REVIEW. SUZUKI, AKIRA. HALOBORATION AND ITS APPLICATION TO ORGANIC SYNTHESIS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  164996. GABRIEL WEATHERHEAD
  164997. 10438N
  164998. 2/28/96V
  164999. A REVIEW. HU, NAN XING; ASO, YOSHIO; OTSUBO, TETSUO; OGURA, FUMIO. ARENETELLURINIC ANHYDRIDES AS NEW SYNTHETIC REAGENTS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165000. GABRIEL WEATHERHEAD
  165001. 10439N
  165002. 2/28/96V
  165003. A REVIEW. MURAHASHI, SHUN ICHI; NAOTA, TAKESHI. RUTHENIUM CATALYZED OXIDATIVE TRANSFORMATIONS OF ALCOHOLS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165004. GABRIEL WEATHERHEAD
  165005. 10440N
  165006. 2/28/96V
  165007. A REVIEW. WATARU, ANDO. CHEMISTRY OF ALLENE EPISULFIDES AND THIIRANORADIALENES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165008. GABRIEL WEATHERHEAD
  165009. 10441N
  165010. 2/28/96V
  165011. A REVIEW. ZWANENBURG, BINNE. SULFINE CHEMISTRY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165012. GABRIEL WEATHERHEAD
  165013. 10442N
  165014. 2/28/96V
  165015. A REVIEW. DUNN, PETER J.; RESS, CHARLES W. NOVEL POLYSULFUR POLYNITROGEN CHEMISTRY. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165016. GABRIEL WEATHERHEAD
  165017. 10443N
  165018. 2/28/96
  165019. A REVIEW. CAPOZZI, FRANCESCO, CAPOZZI, GIUSEPPE, MENICHETTI STEFANO. INTRAMOLECULAR CYCLIZATION OF ALKENES AND ALKYNES PROMOTED BY SULPHENYLATING AGENTS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165020. GABRIEL WEATHERHEAD
  165021. 10444N
  165022. 2/28/96V
  165023. A REVIEW. BLOCK, ERIC. SYNTHESIS AND CHEMISTRY OF NEW HETEROATOM SYSTEMS CONTAINING BOTH SULFUR AND SILICON. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165024. GABRIEL WEATHERHEAD
  165025. 10445N
  165026. 2/28/96
  165027. A REVIEW. CERVEAU, G.; CHUIT, C.; CORRIU, R. J. P.; REYE, C. REACTIVITY OF DIANIONIC HEXACOORDINATED SILICON COMPLEXES TOWARDS NUCLEOPHILES: A NEW WAY TO ORGANOSILANES DIRECTLY FROM SILICA. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.
  165028. GABRIEL WEATHERHEAD
  165029. 10446N
  165030. 2/28/96
  165031. A REVIEW. DU MONT, WOLF W. PROPERTIES OF SE SE AND TE TE BONDS, VII: ACTIVATION OF HOMONUCLEAR SINGLE BONDS BY STERIC STRAIN. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165032. GABRIEL WEATHERHEAD
  165033. 10447N
  165034. 2/28/96V
  165035. A REVIEW. MUSKER, W. KENNETH, DOI, JOYCE TAKAHASHI. HETEROCYCLIC INTERMEDIATES AND PRODUCTS FORMED ON OXIDATIVE CLEAVAGE OF DISULFIDES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165036. GABRIEL WEATHERHEAD
  165037. 10448N
  165038. 2/28/96V
  165039. A REVIEW. SEPPELT, KONRAD; SCHMUCK, ARNO. STRUCTURE AND BONDING OF PENTAPHENYLBISMUTH, BI(C6H5)5 OR: WHY IS BI(C6H5)5 BLUE VIOLET? REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165040. GABRIEL WEATHERHEAD
  165041. 10449N
  165042. 2/28/96
  165043. A REVIEW. MICHALSKI, JAN; LOPUSINSKI, ANDRZEJ. ORGANOPHOSPHORUS THIOCYANIDATES >P(O)SCN AND THEIR STRUCTURAL ANALOGUES. MECHANISM OF THIOCYANIDATE ISOTHIOCYANIDATE ISOMERIZATION. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.
  165044. GABRIEL WEATHERHEAD
  165045. 10450N
  165046. 2/28/96V
  165047. A REVIEW. KING, J. F.; KHEMANI, K. C.; SKONIECZNY, S.; PAYNE, N. C. SULFONYL MECHANISMS: EVIDENCE FOR A STEREOELECTRONIC EFFECT. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165048. GABRIEL WEATHERHEAD
  165049. 10451N
  165050. 2/28/96V
  165051. A REVIEW. BORTOLINI, OLGA, DI FURIA, FULVIO  LICINI, GIULIA, MODENA GIORGIO. STRUCTURE BEHAVIOR RELATIONSHIP IN THE ENANTIOSELECTIVE OXIDATION OF SULFIDES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165052. GABRIEL WEATHERHEAD
  165053. 10452N
  165054. 2/28/96
  165055. A REVIEW. OKUYAMA, TADASHI. STABILITY AND REACTIVITY OF DITHIO CARBOCATIONS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165056. GABRIEL WEATHERHEAD
  165057. 10453N
  165058. 2/28/96V
  165059. A REVIEW. GLASS, RICHARD S., ANDRUSKI, STEPHEN W., BROEKER JEFFREY L. GEOMETRIC EFFECTS IN SULFUR LONE PAIR INTERACTIONS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165060. GABRIEL WEATHERHEAD
  165061. 10454N
  165062. 2/28/96V
  165063. A REVIEW. IWAMURA,HIIZU. HIGH SPINPOLYCARBENES. INPURSUIT OF ORGANIC FERROMAGNETS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165064. GABRIEL WEATHERHEAD
  165065. 10455N
  165066. 2/28/96V
  165067. A REVIEW. OAE, SHIGERU. CHEMICAL BEHAVIOR OF ELEMENTAL SULFUR. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 1, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1988.a
  165068. GABRIEL WEATHERHEAD
  165069. 10456N
  165070. 2/28/96
  165071. A REVIEW. PEARCE, H. L. MEDICINAL CHEMISTRY OF BISINDOLE ALKALOIDS FROM CATHARANTHUS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 37, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165072. GABRIEL WEATHERHEAD
  165073. 10457N
  165074. 2/28/96V
  165075. A REVIEW. BORMAN, LINDA S., KUEHNE, MARTIN E. FUNCTIONAL HOT SPOT AT THE C 20' POSITION OF VINHLASTINE. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 37, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165076. GABRIEL WEATHERHEAD
  165077. 10458N
  165078. 2/28/96V
  165079. A REVIEW. KUEHNE, MARTIN E., MARKO, ISTVAN. SYNTHESES OF VINBLASTINE TYPE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 37, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165080. GABRIEL WEATHERHEAD
  165081. 10459N
  165082. 2/28/96
  165083. A REVIEW. BLASKO, GABOR  CORDELL, GEOFFREY A. ISOLATION STRUCTURE ELUCIDATION, AND BIOSYNTHESIS OF THE BISINDOLE AIKALOIDS OF CATHARONTHUS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 37, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165084. GABRIEL WEATHERHEAD
  165085. 10460N
  165086. 2/28/96V
  165087. A REVIEW. THIEM, JOACHIM; KLAFFKE, WERNER. SYNTHESES OF DEOXY OLIGOSACCHARIDES. 1990, 154 (CARBOHYDRATE CHEMISTRY), 285 332. TOPICS IN CURRENT CHEMISTRYa
  165088. GABRIEL WEATHERHEAD
  165089. 10461N
  165090. 2/28/96V|A REVIEW. SUAMI, TETSUO. CHEMISTRY OF PSEUDO SUGARS. 1990,154 (CARBOHYDRATE CHEMISTRY), 257 283. TOPICS IN CURRENT CHEMISTRYa
  165091. GABRIEL WEATHERHEAD
  165092. 10462N
  165093. 2/28/96V
  165094. A REVIEW. STANEK, JAN. PREPARATION OF SELECTIVELY ALKYLATED SACCHARIDES AS SYNTHETIC INTERMEDIATES. 1990,154 (CARBOHYDRATE CHEMISTRY), 209 256. TOPICS IN CURRENT CHEMISTRYa
  165095. GABRIEL WEATHERHEAD
  165096. 10463N
  165097. 2/28/96
  165098. A REVIEW. MEYER, BERND. CONFORMATIONAL ASPECTS OF OLIGOSACCHARIDES. 1990, 154 (CARBOHYDRATE CHEMISTRY), 141 208. TOPICS IN CURRENT CHEMISTRYa
  165099. GABRIEL WEATHERHEAD
  165100. 10464N
  165101. 2/28/96V
  165102. A REVIEW. GIGG, .JILL; GIGG, ROY. SYNTHESIS OF GLYCOLIPIDS. 1990,154 (CARBOHYDRATE CHEMISTRY), 77 139. TOPICS IN CURRENT CHEMISTRYa
  165103. GABRIEL WEATHERHEAD
  165104. 10465N
  165105. 2/28/96V
  165106. A REVIEW. DESCOTES, GERARD. SYNTHETIC SACCHARIDE PHOTOCHEMISTRY. 1990, 154 (CARBOHYDRATE CHEMISTRY), 39 76. TOPICS IN CURRENT CHEMISTRYa
  165107. GABRIEL WEATHERHEAD
  165108. 10466N
  165109. 2/28/96V
  165110. A REVIEW. BUNDLE, DAVID R. SYNTHESIS OF OLIGOSACCHARIDES RELATED TO BACTERIAL O ANTIGENS. 1990,154 (CARBOHYDRATE CHEMISTRY), 1 37. TOPICS IN CURRENT CHEMISTRYa
  165111. GABRIEL WEATHERHEAD
  165112. 10467N
  165113. 2/28/96V|A REVIEW. BALCI, METIN; SUTBEYAZ, YASAR; SECEN, HASAN. CONDURITOLS AND RELATED COMPOUNDS. 1990, 46(11), 3715 42. TETRAHEDRONa
  165114. GABRIEL WEATHERHEAD
  165115. 10468
  165116. 2/28/96V
  165117. A REVIEW. CARDILLO, GIULIANA; ORENA, MARIO. STEREOCONTROLLED CYCLOFUNCTIONALIZATIONS OF DOUBLE BONDS THROUGH HETEROCYCLIC INTERMEDIATES. 1990, 46(10), 3321 408. TETRAHEDRONa
  165118. GABRIEL WEATHERHEAD
  165119. 10469N
  165120. 2/28/96VyA REVIEW. LAMBERT, JOSEPH B. THE INTERACTION OF SILICON WITH POSITIVELY CHARGED CARBON. 1990, 46(8), 2677 89. TETRAHEDRONa
  165121. GABRIEL WEATHERHEAD
  165122. 10470N
  165123. 2/28/96V{A REVIEW. STAMMER, CHARLES H. CYCLOPROPANE AMINO ACIDS (2,3  AND 3,4 METHANOMAINO ACIDS). 1990, 46(7), 2231 54. TETRAHEDRONa
  165124. GABRIEL WEATHERHEAD
  165125. 10471N
  165126. 2/28/96V
  165127. A REVIEW. TRAMONTINI, MAURILIO, ANGIOLINI, LUIGI. FURTHER ADVANCES IN THE CHEMISTRY OF MANNICH BASES. 1990, 46(6),1791 1837. TETRAHEDRONa
  165128. GABRIEL WEATHERHEAD
  165129. 10472N
  165130. 2/28/96VxA REVIEW. THEBTARANONTH, C., THEBTARANONTH Y. DEVELOPMENTS IN CYCLIZATION REACTIONS. 1990, 46(5), 1385 1489. TETRAHEDRONa
  165131. GABRIEL WEATHERHEAD
  165132. 10473N
  165133. 2/28/96
  165134. A REVIEW. KROHN, K. SYNTHESIS OF ANTHRACYCLINONES BY ELECTROPHILIC AND NUCLEOPHILIC ADDITION TO ANTHRAQUINONES. 1990, 46(2), 291 318. TETRAHEDRONa
  165135. GABRIEL WEATHERHEAD
  165136. 10474N
  165137. 2/28/96V
  165138. A REVIEW. PAGE, PHILIP C. BULMAN; VAN NIEL, MONIQUE B.; PRODGER, JEREMY C. SYNTHETIC USES OF THE 1,3 DITHIANE GROUPING FROM 1977 TO 1988. 1989, 45(24), 7643 77. TETRAHEDRONa
  165139. GABRIEL WEATHERHEAD
  165140. 10475N
  165141. 2/28/96VqA REVIEW. TOMIOKA, KIYOSHI. ASYMMETRIC SYNTHESIS UTILIZING EXTERNAL CHIRAL LIGANDS. 1990, NO. 7, 541 9. SYNTHESISa
  165142. GABRIEL WEATHERHEAD
  165143. 10476N
  165144. 2/28/96V
  165145. A REVIEW. MORIARTY, ROBERT M.; VAID, RADHE K. CARBON CARBON BOND FORMATION VIA HYPERVALENT IODINE OXIDATIONS. 1990, NO. 6, 431 47. SYNTHESISa
  165146. GABRIEL WEATHERHEAD
  165147. 10477N
  165148. 2/28/96V
  165149. A REVIEW. SATO, TADASHI. ANIONIC ORGANOTIN COMPOUNDS IN ORGANIC SYNTHESIS. TRIALKYLSTANNYLLITHIUM AND TRIALKYLSTANNYLMETHYLLITHIUM. 1990, NO. 4, 259 70. SYNTHESIS
  165150. GABRIEL WEATHERHEAD
  165151. 10478N
  165152. 2/28/96V
  165153. A REVIEW. VINNIK, M. F.; OBRAZTSOV, P. A. THE MECHANISM OF THE DEHYDRATION OF ALCOHOLS AND HYDRATION OF ALKENES IN ACID SOLUTION. 1990, 59(1),106 31. RUSSIAN CHEMICAL REVIEWSa
  165154. GABRIEL WEATHERHEAD
  165155. 10479N
  165156. 2/28/96V
  165157. A REVIEW. KUKHAR', V. P., YAGUPOL'SKII, YU L.; SOLOSHONOK, V. A. ,B FLUORO SUBSTITUTED AMINOACIDS. 1990, 59(1),89 102. RUSSIAN CHEMICAL REVIEWSa
  165158. GABRIEL WEATHERHEAD
  165159. 10480N
  165160. 2/28/96V
  165161. A REVIEW. PROIDAKOV, A. G., KALABIN, G. A., VASILEVSKII, S. F. THE PARAMETERS OF THE CARBON 13 NMR SPECTRA OF SUBSTITUTED ACETYLENES: RELATION WITH ELECTRONIC STRUCTURE AND REACTIVITY. 1990, 59(1), 23 38. RUSSIAN CHEMICAL REVIEWSa
  165162. GABRIEL WEATHERHEAD
  165163. 10481N
  165164. 2/28/96V
  165165. A REVIEW. KAITMAZOVA, G. S.; GAMBARYAN, N. P.; ROKHLIN, E. M. AMINES ACTING AS HYDRIDE ION DONORS IN REACTIONS WITH UNSATURATED ELECTROPHILIC COMPOUNDS. 1989, 58(12),114,~1157. RUSSIAN CHEMICAL REVIEWS
  165166. GABRIEL WEATHERHEAD
  165167. 10482N
  165168. 2/28/96V
  165169. A REVIEW. KOZHUSHKO, B. N.; LOMAKINA, A. V.; SHOKOL, V. A. PHOSPHORUS CONTAINING ALKYL, ALKENYL, ARYL, ACYL AND SULPHONYL ISOCYANATES. 1989, 58(11), 1062 1076. RUSSIAN CHEMICAL REVIEWSa
  165170. GABRIEL WEATHERHEAD
  165171. 10483N
  165172. 2/28/96V
  165173. A REVIEW. LABEISH, N. N.; PETROV, A. A. REACTIONS INVOLVING THE ADDITION OF N HALOGENO AMIDES TO UNSATURATED COMPOUNDS. 1989, 58(11), 1048 61. RUSSIAN CHEMICAL REVIEWSa
  165174. GABRIEL WEATHERHEAD
  165175. 10484N
  165176. 2/28/96V
  165177. A REVIEW. KUZNETSOV, A. I., ZEFIROV, N. S. AZAADAMANTANES WITH NITROGEN ATOMS IN THE BRIDGEHEAD POSITIONS. 1989, 58(11), 1033 47. RUSSIAN CHEMICAL REVIEWSa
  165178. GABRIEL WEATHERHEAD
  165179. 10485N
  165180. 2/28/96V
  165181. A REVIEW. KOLBANOVSKII, YU. A. THE METHOD OF ADIABATIC COMPRESSION IN KINETIC AND MECHANISTIC INVESTIGATIONS OF REACTIONS WITH THE PARTICIPATION OF FLUORINE CONTAINING CARBENES. 1989, 58(11), 1024 32. RUSSIAN CHEMICAL REVIEWS
  165182. GABRIEL WEATHERHEAD
  165183. 10486N
  165184. 2/28/96V
  165185. A REVIEW. GLEBOV, L. S.; KLIGER, G. A. SYNTHESES OF ORGANIC COMPOUNDS IN THE PRESENCE OF THE FUSED IRON CATALYST AND THEIR MECHANISMS AND KINETICS. 1989, 58(10), 977 91. RUSSIAN CHEMICAL REVIEWSa
  165186. GABRIEL WEATHERHEAD
  165187. 10487N
  165188. 2/28/96VpA REVIEW. TROFIMOV, B. A. PROSPECTS FOR THE CHEMISTRY OF PYRROLE. 1989, 58(10), 967 76. RUSSIAN CHEMICAL REVIEWSa
  165189. GABRIEL WEATHERHEAD
  165190. 10488N
  165191. 2/28/96V
  165192. A REVIEW. RADCHENKO, S. I.; PETROV, A. A ACETYLENIC ETHERS AND THEIR ANALOGUES. 1989, 58(10), 948 966. RUSSIAN CHEMICAL REVIEWSa
  165193. GABRIEL WEATHERHEAD
  165194. 10489N
  165195. 2/28/96V
  165196. A REVIEW. MARTYNOV, 1. V.; YURTANOV, A. I. A HALO A NITROCARBOXYLIC ACIDS AND THEIR DERIVATIVES. 1989, 58(9), 848 62. RUSSIAN CHEMICAL REVIEWSa
  165197. GABRIEL WEATHERHEAD
  165198. 10490N
  165199. 2/28/96
  165200. ~VtA REVIEW. MAKOSZA, M. VICARIOUS NUCLEOPHILIC SUBSTITUTION OF HYDROGEN. 1989, 58(8), 747 57. RUSSIAN CHEMICAL REVIEWSa
  165201. GABRIEL WEATHERHEAD
  165202. 10491N
  165203. 2/28/96V
  165204. A REVIEW. KUZNETSOV, M. A.; IOFFE, B. V. THE PRESENT STATE OF THE CHEMISTRY OF AMINONITRENES AND OXYNITRENES. 1989, 58(8), 732 46. RUSSIAN CHEMICAL REVIEWSa
  165205. GABRIEL WEATHERHEAD
  165206. 10492N
  165207. 2/28/96V
  165208. A REVIEW. MANDEL'SHTAM, T. V. CARBONYLCARBENES IN THE SPECIFIC SYNTHESIS OF NATURAL PRODUCTS. 1989, 58(8), 720 31. RUSSIAN CHEMICAL REVIEWSa
  165209. GABRIEL WEATHERHEAD
  165210. 10493N
  165211. 2/28/96V
  165212. A REVIEW. KULINKOVICH 0. G. CARBENE METHODS FOR THE INTRODUCTION OF ACYL AND ACYLMETHYL GROUPS INTO ORGANIC MOLECULES. 1989, 58(8), 711 19. RUSSIAN CHEMICAL REVIEWSa
  165213. GABRIEL WEATHERHEAD
  165214. 10494N
  165215. 2/28/96
  165216. A REVIEW. WENDER, PAUL A.; TERNANSKY, ROBERT; DELONG, MITCH; SINGH, SUNIL; OLIVERO, ALAN; RICE, KEN. ARENE ALKENE CYCLOADDITIONS AND ORGANIC SYNTHESIS. 1990, 62(8),1597 602. PURE AND APPLIED CHEMISTRYa
  165217. GABRIEL WEATHERHEAD
  165218. 10495N
  165219. 2/28/96V
  165220. A REVIEW. JONAS, KLAUS. NEW FINDINGS IN THE ARENE CHEMISTRY OF THE 3D TRANSITION METALS. 1990, 62(6), 1169 74. PURE AND APPLIED CHEMISTRYa
  165221. GABRIEL WEATHERHEAD
  165222. 10496N
  165223. 2/28/96V
  165224. A REVIEW. ASTRUC, D.; HAMON, J. R.; MANDON, D.; MOULINES, F. ASPECTS OF AROMATIC IRON SANDWICHES: APPLICATION TO ORGANIC AND ORGANOMETALLIC SYNTHESIS. 1990, 62(6), 1165 8. PURE AND APPLIED CHEMISTRYa
  165225. GABRIEL WEATHERHEAD
  165226. 10497N
  165227. 2/28/96V
  165228. A REVIEW. VAN KOTEN, GERARD. NOVEL ASPECTS OF H' DIIODINE COORDINATION AND DIIODINE OXIDATIVE ADDITION TO PLATINUM(II) AND HALIDE TRANSFER OXIDATION REACTIONS OF ORGANOPLATINIUM(II) AND CUIIX2. 1990, 62(6),1155 9. PURE AND APPLIED CHEMISTRYa
  165229. GABRIEL WEATHERHEAD
  165230. 10498N
  165231. 2/28/96V
  165232. A REVIEW. TANAKA, MASATO; SAKAKURA, TOSHIYASU. PHOTOCATALYTIC CARBON HYDROGEN ACTIVATION BY RHCL(CO)(PME3)2. 1990, 62(6), 1147 50. PURE AND APPLIED CHEMISTRYa
  165233. GABRIEL WEATHERHEAD
  165234. 10499N
  165235. 2/28/96V
  165236. A REVIEW. WILD, S. BRUCE. HIGHLY STEREOSELECTIVE SYNTHESES OF ARSENIC AND PHOSPHORUS MACROCYCLES AND CAGES. 1990, 62(6), 1139 44. PURE AND APPLIED CHEMISTRYa
  165237. GABRIEL WEATHERHEAD
  165238. 10500N
  165239. 2/28/96VbA REVIEW. COOPER, STEPHEN R. SUPERTRIPODAL LIGANDS. 1990,62(6), 1123 5. PURE AND APPLIED CHEMISTRYa
  165240. GABRIEL WEATHERHEAD
  165241. 10501N
  165242. 2/28/96V
  165243. A REVIEW. PERUTZ, ROBIN N. PHOTOCHEMICAL CARBON HYDROGEN BOND ACTIVATION; NMR, MATRIX, AND LASER KINETIC STUDIES. 1990, 62(6), 1103 6. PURE AND APPLIED CHEMISTRYa
  165244. GABRIEL WEATHERHEAD
  165245. 10502N
  165246. 2/28/96V
  165247. A REVIEW. JUTZI, PETER. P COORDINATION TO MAIN GROUP ELEMENTS
  165248.  SOME NEW RESULTS. 1990, 62(6), 1035 8. PURE AND APPLIED CHEMISTRY
  165249. GABRIEL WEATHERHEAD
  165250. 10503N
  165251. 2/28/96V
  165252. A REVIEW. BRUCE, MICHAEL 1. CARBENES, CARBIDES, AND CARBON. TEN YEARS OF TRANSITION METAL ACETYLENE CHEMISTRY. 1990, 62(6), 1021 6. PURE AND APPLIED CHEMISTRYa
  165253. GABRIEL WEATHERHEAD
  165254. 10504N
  165255. 2/28/96V
  165256. A REVIEW. IMAMOTO, TSUNEO. CARBONYL ADDITION REACTIONS PROMOTED BY CERIUM REAGENTS. 1990, 62(4), 747 52. PURE AND APPLIED CHEMISTRYa
  165257. GABRIEL WEATHERHEAD
  165258. 10505N
  165259. 2/28/96V
  165260. A REVIEW. LEHMKUHL, HERBERT. SPECIFIC REACTIONS OF ORGANYLMETAL COMPLEXES WITH UNSATURATED HYDROCARBONS. 1990, 62(4), 731 40. PURE AND APPLIED CHEMISTRYa
  165261. GABRIEL WEATHERHEAD
  165262. 10506N
  165263. 2/28/96V
  165264. A REVIEW. CACCHI, SANDRO. THE PALLADIUM CATALYZED HYDROARYLATION AND HYDROVINYLATION OF CARBON CARBON MULTIPLE BONDS: NEW PERSPECTIVES IN ORGANIC SYNTHESIS. 1990, 62(4), 713 22. PURE AND APPLIED CHEMISTRYa
  165265. GABRIEL WEATHERHEAD
  165266. 10507N
  165267. 2/28/96
  165268. A REVIEW. MOLANDER GARY A.; MAUTNER, KONRAD. NOVEL PROCESSES FOR STEREOSEIECTIVE ORGANIC SYNTHESIS. 1990, 62(4), 707 12. PURE AND APPLIED CHEMISTRYa
  165269. GABRIEL WEATHERHEAD
  165270. 10508N
  165271. 2/28/96VuA REVIEW. BICKELHAUPT, FRIEDRICH. NEW TRENDS IN DIMETALLIC SYNTHONS. 1990, 62(4), 699 706. PURE AND APPLIED CHEMISTRYa
  165272. GABRIEL WEATHERHEAD
  165273. 10509N
  165274. 2/28/96V
  165275. A REVIEW. HEGEDUS, LOUIS S. CHROMIUM CARBENE COMPLEXES IN THE SYNTHESIS OF MOLECULES OF BIOLOGICAL INTEREST. 1990, 62(4), 691 8. PURE AND APPLIED CHEMISTRYa
  165276. GABRIEL WEATHERHEAD
  165277. 10510N
  165278. 2/28/96V
  165279. A REVIEW. SNIECKUS, V. REGIOSELECTIVE SYNTHETIC PROCESSES BASED ON THE AROMATIC DIRECTED METALATION STRATEGY. 1990, 62(4), 1 80. PURE AND APPLIED CHEMISTRYa
  165280. GABRIEL WEATHERHEAD
  165281. 10511N
  165282. 2/28/96V
  165283. A REVIEW. LAROCK, RICHARD C. NEW APPLICATIONS OF ORGANOPALLADIUM COMPOUNDS IN ORGANIC SYNTHESIS. 1990, 62(4), 653 60. PURE AND APPLIED CHEMISTRYa
  165284. GABRIEL WEATHERHEAD
  165285. 10512N
  165286. 2/28/96V
  165287. A REVIEW. DUTHALER, RUDOLF 0.; HAFNER, ANDREAS; RIEDIKER, MARTIN. ASYMMETRIC CARBON CARBON BOND FORMATION WITH TITANIUM CARBOHYDRATE COMPLEXES. 1990, 62(4), 631 42. PURE AND APPLIED CHEMISTRYa
  165288. GABRIEL WEATHERHEAD
  165289. 10513N
  165290. 2/28/96V
  165291. A REVIEW. CATELLANI MARTA, CHIUSOLI, GIAN PAOLO  COSTA, MIRCO. SOME PALLADIUM CATALYZED CARBON CARBON BOND FORMATION REACTIONS. 1990, 62(4), 623 30. PURE AND APPLIED CHEMISTRYa
  165292. GABRIEL WEATHERHEAD
  165293. 10514N
  165294. 2/28/96V
  165295. A REVIEW. NOYORI, R., UCHIYAMA, M., KATO, H. WAKABAYASHI, S. HAYAKAWA, Y. ORGANOMETALLIC METHODOLOGIES FOR NUCLEIC ACID SYNTHESIS. 1990, 62(4), 613 22. PURE AND APPLIED CHEMISTRYa
  165296. GABRIEL WEATHERHEAD
  165297. 10515N
  165298. 2/28/96
  165299. A REVIEW. CAINELLI, GIANFRANCO, PANUNZIO, MAURO  ANDREOLI, PATRIZIA; MARTELLI, GIORGIO; SPUNTA, GIUSEPPE; GIACOMINI, DARIA; BANDINI, ELISA. METALLO IMINES: USEFUL REAGENTS IN ORGANIC SYNTHESIS. 1990, 62(4), 605 12. PURE AND APPLIED CHEMISTRYa
  165300. GABRIEL WEATHERHEAD
  165301. 10516N
  165302. 2/28/96V
  165303. A REVIEW. BARLUENGA, JOSE. PREPARATION AND SOME APPLICATIONS OF FUNCTIONALIZED ORGANO LITHIUM COMPOUNDS IN ORGANIC SYNTHESIS. 1990, 62(4), 595 604. PURE AND APPLIED CHEMISTRYa
  165304. GABRIEL WEATHERHEAD
  165305. 10517N
  165306. 2/28/96V
  165307. A REVIEW. BRUNNER, HENRI. RIGHT OR LEFT
  165308. THIS IS THE QUESTION (ENANTIOSELECTIVE CATALYSIS WITH TRANSITION METAL COMPOUNDS). 1990, 62(4), 589 94. PURE AND APPLIED CHEMISTRYa
  165309. GABRIEL WEATHERHEAD
  165310. 10518N
  165311. 2/28/96V
  165312. A REVIEW. ITO, YOSHIHIKO. NEW METALATION AND SYNTHETIC APPLICATIONS OF ISONITRILES. 1990, 62(4), 583 8. PURE AND APPLIED CHEMISTRYa
  165313. GABRIEL WEATHERHEAD
  165314. 10519N
  165315. 2/28/96
  165316. A REVIEW. DICKENS, P. J.; GILDAY, J. P.; NEGRI, J. T.; WIDDOWSON, D. A. CHROMIUM DIRECTED REGIO  AND STEREOCONTROL: A NEW CHAPTER IN AROMATIC NATURAL PRODUCT SYNTHESIS. 1990, 62(4), 575 81. PURE AND APPLIED CHEMISTRYa
  165317. GABRIEL WEATHERHEAD
  165318. 10520N
  165319. 2/28/96V^A REVIEW. VOGEL, EMANUEL. NOVEL PORPHYRINOIDS. 1990, 62(3), 557 64. PURE AND APPLIED CHEMISTRYa
  165320. GABRIEL WEATHERHEAD
  165321. 10521N
  165322. 2/28/96V
  165323. A REVIEW. SUGIMOTO, TOYONARI; YOSHIDA, ZENICHI. OVERALL VIEW OF CYCLIC POLYCALICENYLS. 1990, 62(3), 551 6. PURE AND APPLIED CHEMISTRYa
  165324. GABRIEL WEATHERHEAD
  165325. 10522N
  165326. 2/28/96V
  165327. A REVIEW. HALTON, BRIAN. ALKYLIDENECYCLOPROPARENES: STRAINED AND POLAR AROMATICS. 1990, 62(3), 541 6. PURE AND APPLIED CHEMISTRYa
  165328. GABRIEL WEATHERHEAD
  165329. 10523N
  165330. 2/28/96V
  165331. A REVIEW. NAKASUJI, KAZUHIRO. NEW MULTI STAGE REDOX SYSTEMS AND NEW ORGANIC MOLECULAR METALS. 1990, 62(3), 477 82. PURE AND APPLIED CHEMISTRYa
  165332. GABRIEL WEATHERHEAD
  165333. 10524N
  165334. 2/28/96V
  165335. A REVIEW. HARADA, YOSHIYA. PENNING IONIZATION ELECTRON SPECTROSCOPY OF ORGANIC MOLECULES: STEREOCHEMISTRY OF MOLECULAR ORBITALS. 1990, 62(3), 457 62. PURE AND APPLIED CHEMISTRYa
  165336. GABRIEL WEATHERHEAD
  165337. 10525N
  165338. 2/28/96V
  165339. A REVIEW. HOSOYA, H. KUMAZAKI, H.; CHIDA, K.; OHUCHI, M.; GAO, Y. D. HOW DO THE POLYCYCLIC AROMATIC HYDROCARBONS APPROACH INFINITY? 1990, 62(3), 445 50. PURE AND APPLIED CHEMISTRYa
  165340. GABRIEL WEATHERHEAD
  165341. 10526N
  165342. 2/28/96V
  165343. A REVIEW. BICKELHAUPT, FRIEDRICH. SMALL CYCLOPHANES: THE BENT BENZENE BUSINESS. 1990, 62(3), 373 32. PURE AND APPLIED CHEMISTRYa
  165344. GABRIEL WEATHERHEAD
  165345. 10527N
  165346. 2/28/96V
  165347. A REVIEW. KRYGOWSKI, TADEUSZ MAREK. CORRELATION ANALYSIS IN ORGANIC CRYSTAL CHEMISTRY. 1990,17, 239 291. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165348. GABRIEL WEATHERHEAD
  165349. 10528N
  165350. 2/28/96
  165351. A REVIEW. GAL, JEAN FRANC,OIS; MARIA, PIERRE CHARLES. CORRELATION ANALYSIS OF ACIDITY AND BASICITY: FROM THE SOLUTION TO THE GAS PHASE. 1990,17,159 238. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165352. GABRIEL WEATHERHEAD
  165353. 10529N
  165354. 2/28/96V
  165355. A REVIEW. BENTLEY, T. WILLIAM, LLEWELLYN, GARETH. YX SCALES OF SOLVENT IONIZING POWER. 1990, 17, 121 158. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165356. GABRIEL WEATHERHEAD
  165357. 10530N
  165358. 2/28/96V
  165359. A REVIEW. TOPSOM, R. D. THEORETICAL STUDIES OF THE EFFECTS OF HYDRATION ON ORGANIC EQUILIBRIA. 1990,17, 107 120. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165360. GABRIEL WEATHERHEAD
  165361. 10531N
  165362. 2/28/96V
  165363. A REVIEW. GRUNWALD, ERNEST. REACTION COORDINATES AND STRUCTURE ENERGY RELATIONSHIPS. 1990, 17, 55 105. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165364. GABRIEL WEATHERHEAD
  165365. 10532N
  165366. 2/28/96
  165367. VxA REVIEW. GRUNWALD, ERNEST. THERMODYNAMICS OF MOLECULAR SPECIES. 1990, 17, 31 53. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165368. GABRIEL WEATHERHEAD
  165369. 10533N
  165370. 2/28/96VfA REVIEW. SHORTER,JOHN. HAMMETT MEMORIAL LECTURE. 1990,17,1 29. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  165371. GABRIEL WEATHERHEAD
  165372. 10534N
  165373. 2/28/96VSA REVIEW. PINNICK, HAROLD W. THE NEF REACTION. 1990, 38, 655 792. ORGANIC REACTIONSa
  165374. GABRIEL WEATHERHEAD
  165375. 10535N
  165376. 2/28/96V
  165377. A REVIEW. CHAPDELAINE, MARC J.; HULCE, MARTIN. TANDEM VICINAL DIFUNCTIONALIZATION: B ADDITION TO A,B UNSATURATED CARBONYL SUBSTRATES FOLLOWED BY A FUNCTIONALIZATION. 1990, 38, 225 653. ORGANIC REACTIONSa
  165378. GABRIEL WEATHERHEAD
  165379. 10536N
  165380. 2/28/96V^A REVIEW. AGER, DAVID J. THE PETERSON OLEFINATION REACTION. 1990, 38, 1 223. ORGANIC REACTIONSa
  165381. GABRIEL WEATHERHEAD
  165382. 10537N
  165383. 2/28/96
  165384. A REVIEW. FLEMING, IAN; DUNOGUES, JACQUES; SMITHERS, ROGER. THE ELECTROPHILIC SUBSTITUTION OF ALLYLSILANES AND VINYLSILANES. 1989, 37, 57 575. ORGANIC REACTIONSa
  165385. GABRIEL WEATHERHEAD
  165386. 10538N
  165387. 2/28/96V
  165388. A REVIEW. OHNO, MASAJI; OTSUKA, MASAMI. CHIRAL SYNTHONS BY ESTER HYDROLYSIS CATALYZED BY PIG LIVER ESTERASE. 1989, 37,1 55. ORGANIC REACTIONSa
  165389. GABRIEL WEATHERHEAD
  165390. 10539N
  165391. 2/28/96V`A REVIEW. ENGEL, ROBERT. PHOSPHORUS ADDITION AT SP2 CARBON. 1988, 36, 173 248. ORGANIC REACTIONSa
  165392. GABRIEL WEATHERHEAD
  165393. 10540N
  165394. 2/28/96V
  165395. A REVIEW. CONFALONE, PAT N.; HUIE, EDWARD M. THE [3 + 2] NITRONE OLEFIN CYCLOADDITON REACTION. 1988, 36, 1 173. ORGANIC REACTIONSa
  165396. GABRIEL WEATHERHEAD
  165397. 10541N
  165398. 2/28/96V
  165399. A REVIEW. FISHER, LAWRENCE E.; MUCHOWSKI, JOSEPH M. SYNTHESIS OF A AMINO ALDHYDES AND A AMINO KETONES. A REVIEW. 1990, 22(4), 399 484. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  165400. GABRIEL WEATHERHEAD
  165401. 10542N
  165402. 2/28/96V
  165403. A REVIEW. SMITH, MICHAEL B. N DIENYL AMIDES AND LACTAMS. PREPARATION AND DIELS ALDER REACTIVITY. 1990, 22(3), 315 97. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  165404. GABRIEL WEATHERHEAD
  165405. 10543N
  165406. 2/28/96V
  165407. A REVIEW. SCRETTAS, CONSTANTINOS G.; STEELE, BARRY R. ORGANOMETALLIC CARBOXAMIDATION. A REVIEW. 1990, 22(3), 269 314. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  165408. GABRIEL WEATHERHEAD
  165409. 10544N
  165410. 2/28/96V
  165411. A REVIEW. FRINGUELLI, FRANCESO; TATICCHI, ALDO; WENKERT, ERNEST. DIELS ALDER REACTIONS OF CYCLOALKENONES IN ORGANIC SYNTHESIS. A REVIEW. 1990 22(2), 131 65. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  165412. GABRIEL WEATHERHEAD
  165413. 10545N
  165414. 2/28/96V
  165415. A REVIEW. NAKAGAKI, RYOICHI; SAKURAGI, HIROCHIKA; MUTAI, KIYOSHI. SWITCHING OF REACTION PATHWAYS DUE TO METHYLENE CHAIN LENGTH EFFECTS. 1989, 2(3), 187 204. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  165416. GABRIEL WEATHERHEAD
  165417. 10546N
  165418. 2/28/96V
  165419. A REVIEW. KATRITZKY, ALAN R., BRYCKI, BOGUMIL E. NUCLEOPHILIC SUBSTITUTION AT SATURATED CARBON ATOMS. MECHANISMS AND MECHANISTIC BORDERLINES: EVIDENCE FROM STUDIES WITH NEUTRAL IEAVING GROUPS. 1988,1(1), 1 20. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  165420. GABRIEL WEATHERHEAD
  165421. 10547N
  165422. 2/28/96V
  165423. A REVIEW. EBETINO, FRANK H., DEGENHARDT, CHARLES R., JAMIESON, LAURA A.; BRUDSAIL, DON C. RECENT WORK ON THE SYNTHESIS OF PHOSPHONATE CONTAINING, BONE ACTIVE HETEROCYCLES. 1990, 30(SPECIAL ISSUE NO. 2), 855 62. HETEROCYCLESa
  165424. GABRIEL WEATHERHEAD
  165425. 10548N
  165426. 2/28/96
  165427. A REVIEW. ALPEGIANI, MARCO, BEDESCHI, ANGELO, GIUDICI, FRANCO; PERRONE, ETTORE, VISENTIN, GIUSEPPINA, ZARINI, FRANCO FRANCESCHI, GIOVANNI. 2 (HETEROATOM SUBSTITUTED)METHYL PENEMS. IV. OXYGEN DERIVATIVES. 1990, 30(SPECIAL ISSUE NO. 2), 799 812. HETEROCYCLES
  165428. GABRIEL WEATHERHEAD
  165429. 10549N
  165430. 2/28/96
  165431. V{A REVIEW. BURWELL, ROBERT L., JR. MECHANISMS OF HETEROGENEOUS CATALYSIS. 1990, 3(4), 253 279. CHEMTRACTS: ORGANIC CHEMISTRYa
  165432. GABRIEL WEATHERHEAD
  165433. 10550N
  165434. 2/28/96V
  165435. A REVIEW. NOYORI, R.; SUZUKI, M. AN ORGANOMETALLIC WAY TO PROSTAGLANDINS: THE THREE COMPONENT COUPLING SYNTHESIS. 1990, 3(3), 173 197. CHEMTRACTS: ORGANIC CHEMISTRYa
  165436. GABRIEL WEATHERHEAD
  165437. 10551N
  165438. 2/28/96VeA REVIEW. WONG, C. H. ENZYMES IN ORGANIC SYNTHESIS. 1990, 3(2), 91 111. CHEMTRACTS: ORGANIC CHEMISTRYa
  165439. GABRIEL WEATHERHEAD
  165440. 10552N
  165441. 2/28/96V
  165442. A REVIEW. NEGISHI, EIICHI. CYCLIZATION, COUPLING, AND REARRANGEMENT REACTIONS OF ORGANOZIRCONIUM AND RELATED COMPOUNDS. 1989, 29(4), 457 68. CHEMICA SCRIPTAa
  165443. GABRIEL WEATHERHEAD
  165444. 10553N
  165445. 2/28/96
  165446. A REVIEW. ERKER, GERHARD, AULBACH, MICHAEL, MENA, MIGUEL, PFAFF RONALD, SOSNA, FRIEDRICH. CARBON CARBON BOND FORMATION BY MEANS OF ZIRCONOCENE DERIVED CARBENE COMPLEXES. 1989, 29(4), 451 6. CHEMICA SCRIPTAa
  165447. GABRIEL WEATHERHEAD
  165448. 10554N
  165449. 2/28/96V
  165450. A REVIEW. KING, STEVEN A.; MILLER, JOHN B.; WONG, ANTHONY C. C.; SCHWARTZ, JEFFREY. ORGANOZIRCONIUM CHEMISTRY REVISITED: ON THE SURFACE THINGS DON'T LOOK QUITE THE SAME. 1989, 29(4), 411 15. CHEMICA SCRIPTAa
  165451. GABRIEL WEATHERHEAD
  165452. 10555N
  165453. 2/28/96V
  165454. A REVIEW. SATCHELL, DEREK P. N., SATCHELL, ROSEMARY S. MECHANISMS OF HYDROLYSIS OF THIOACETALS. 1990,19(1), 55 81. CHEMICAL SOCIETY REVIEWSa
  165455. GABRIEL WEATHERHEAD
  165456. 10556N
  165457. 2/28/96VrA REVIEW. KOCHETKOV, N. K. MICROBIAL POLYSACCHARIDES: NEW APPROACHES. 1990, 19(1), 29 54. CHEMICAL SOCIETY REVIEWSa
  165458. GABRIEL WEATHERHEAD
  165459. 10557N
  165460. 2/28/96
  165461. A REVIEW. WARD, R. S. NONENZYMIC ASYMMETRIC TRANSFORMATIONS INVOLVING SYMMETRICAL BIFUNCTIONAL COMPOUNDS. 1990,19(1), 1 19. CHEMICAL SOCIETY REVIEWSa
  165462. GABRIEL WEATHERHEAD
  165463. 10558N
  165464. 2/28/96V
  165465. A REVIEW. THIBBLIN, ALF, AHLBERG, PER. REACTION BRANCHING AND EXTREME KINETIC ISOTOPE EFFECTS IN THE STUDY OF REACTION MECHANISMS. 1989,18(2), 209 24. CHEMICAL SOCIETY REVIEWSa
  165466. GABRIEL WEATHERHEAD
  165467. 10559N
  165468. 2/28/96V
  165469. A REVIEW. NOYORI, R. CHEMICAL MULTIPLICATION OF CHIRALITY: SCIENCE AND APPLICATIONS. 1989,18(2),187 208. CHEMICAL SOCIETY REVIEWSa
  165470. GABRIEL WEATHERHEAD
  165471. 10560N
  165472. 2/28/96V
  165473. A REVIEW. GORDON, ISOBEL M.; MASKILL, H.; RUASSE, MARIE FRANCOISE. SULFONYL TRANSFER REACTIONS. 1989, 18(2),123 51. CHEMICAL SOCIETY REVIEWSa
  165474. GABRIEL WEATHERHEAD
  165475. 10562N
  165476. 2/28/96VlA REVIEW. PATON, R. MICHAEL. THE CHEMISTRY OF NITRILE SULFIDES. I989, 18(1), 33 52. CHEMICAL SOCIETY REVIEWSa
  165477. GABRIEL WEATHERHEAD
  165478. 10563N
  165479. 2/28/96V
  165480. A REVIEW. SANNIGRABI, A. B.; KAR, T.; NIYOGI, B. GUHA; HOBZA, PAVEL; SCHLEYER, PAUL V. R. THE LITHIUM BOND REEXAMINED. 1990, 90(6), 1061 76. CHEMICAL REVIEWSa
  165481. GABRIEL WEATHERHEAD
  165482. 10564N
  165483. 2/28/96V
  165484. A REVIEW. BRUNET, J. J. TETRACARBONYLHYDRIDOFERRATES, MHFE(C0)4: VERSATILE TOOLS IN ORGANIC SYNTHESIS AND CATALYSIS. 1990, 90(6), 1041 59. CHEMICAL REVIEWSa
  165485. GABRIEL WEATHERHEAD
  165486. 10565N
  165487. 2/28/96VzA REVIEW. MATHEY, FRANCOIS. CHEMISTRY OF 3 MEMBERED CARBONPHOSPHORUS HETEROCYCLES. 1990, 90(6), 997 1025. CHEMICAL REVIEWSa
  165488. GABRIEL WEATHERHEAD
  165489. 10566N
  165490. 2/28/96V
  165491. A REVIEW. SNIECKUS, VICTOR. DIRECTED ORTHO METALATION. TERTIARY AMIDE AND O CARBAMATE DIRECTORS IN SYNTHETIC STRATEGIES FOR POLYSUBSTITUTED AROMATICS. 1990, 90(6), 879 933. CHEMICAL REVIEWSa
  165492. GABRIEL WEATHERHEAD
  165493. 10567N
  165494. 2/28/96
  165495. A REVIEW. UHLMANN, EUGEN  PEYMAN, ANUSCH. ANTISENSE OLIGONUCLEOTIDES: A NEW THERAPEUTIC PRINCIPLE. 1990, 90(4), 543 84. CHEMICAL REVIEWSa
  165496. GABRIEL WEATHERHEAD
  165497. 10568N
  165498. 2/28/96V
  165499. A REVIEW. PAULSEN, HANS. SYNTHESIS, CONFORMATIONS, AND X RAY STRUCTURE ANALYSIS OF SACCHARIDE CHAINS FROM THE CORE REGIONS OF GLYCOPROTEIN. 1990, 29(8), 823 839. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  165500. GABRIEL WEATHERHEAD
  165501. 10569N
  165502. 2/28/96V
  165503. A REVIEW. KLAUI, WOLFGANG. THE COORDINATION CHEMISTRY AND ORGANOMETALLIC CHEMISTRY OF TRIDENTATE OXYGEN LIGANDS WITH P DONOR PROPERTIES. 1990, 29(6), 627 637. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  165504. GABRIEL WEATHERHEAD
  165505. 10570N
  165506. 2/28/96V
  165507. A REVIEW. PAQUETTE, LEO A. STEREOCONTROLLED CONSTRUCTION OF COMPLEX CYCLIC KETONES BY OXY COPE REARRANGEMENT. 1990, 29(6), 6O9 626. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  165508. GABRIEL WEATHERHEAD
  165509. 10571N
  165510. 2/28/96
  165511. A REVIEW. POWER, PHILIP P. BORON PHOSPHORUS COMPOUNDS AND MULTIPLE BONDING. 1990, 29(5), 449 460. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  165512. GABRIEL WEATHERHEAD
  165513. 10572N
  165514. 2/28/96V
  165515. A REVIEW. SANDER, WOLFRAM. ZWITTERIONS OR DIRADICALS? 1990, 29(4), 344 354. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  165516. GABRIEL WEATHERHEAD
  165517. 10573N
  165518. 2/28/96V
  165519. A REVIEW. HOLLINGSWORTH, MARK D.; MCBRIDE, J. MICHAEL. PHOTOCHEMICAL MECHANISM IN SINGLE CRYSTALS: FTIR STUDIES OF DIACYL PEROXIDES. 1990, 15, 279 379. ADVANCES IN PHOTOCHEMISTRYa
  165520. GABRIEL WEATHERHEAD
  165521. 10574N
  165522. 2/28/96V
  165523. A REVIEW. BECKER, HANS DIETER. EXCITED STATE REACTIVITY AND MOLECULAR TOPOLOGY RELATIONSHIPS IN CHROMOPHORICALLY SUBSTITUTED ANTHRACENES. 1990, 15,139 227. ADVANCES IN PHOTOCHEMISTRYa
  165524. GABRIEL WEATHERHEAD
  165525. 10575N
  165526. 2/28/96
  165527. A REVIEW. HEICKLEN, JULIAN. THE DECOMPOSITION OF ALKYL NITRITES AND THE REACTIONS OF ALKOXYL RADICALS. 1988,14,177 272. ADVANCES IN PHOTOCHEMISTRYa
  165528. GABRIEL WEATHERHEAD
  165529. 10576N
  165530. 2/28/96V
  165531. A REVIEW. COLLIN, GUY J. PHOTOCHEMISTRY OF SIMPLE OLEFINS: CHEMISTRY OF ELECTRONIC EXCITED STATES OR HOT GROUND STATE? 1988, 14, 135 176. ADVANCES IN PHOTOCHEMISTRYa
  165532. GABRIEL WEATHERHEAD
  165533. 10577N
  165534. 2/28/96V
  165535. A REVIEW. TISLER, MIHA  STANOVNIK, BRANKO. ADVANCES IN PYRIDAZINE CHEMISTRY. 1990, 49, 385 474. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165536. GABRIEL WEATHERHEAD
  165537. 10578N
  165538. 2/28/96V
  165539. A REVIEW. SHABAN, MOHAMMED A. E., NASR, ADEL Z. SYNTHESIS OF CONDENSED 1,2,4 TRIAZOL[3,4 Z] HETEROCYCLES. 1990, 49, ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165540. GABRIEL WEATHERHEAD
  165541. 10579N
  165542. 2/28/96
  165543. A REVIEW. CRABB, TREVOR A.JACKSON, DAVID; PATEL, ASMITA V. SATURATED BICYCLIC 6/5 RING FUSED SYSTEMS WITH BRIDGEHEAD NITROGEN AND A SINGLE ADDITIONAL HETEROATOM. 1990, 49, 193 275. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165544. GABRIEL WEATHERHEAD
  165545. 10580N
  165546. 2/28/96V
  165547. A REVIEW. VORBRUGGEN, HELMUT. ADVANCES IN AMINATION OF NITROGEN HETEROCYCLES. 1990, 49 117 192. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165548. GABRIEL WEATHERHEAD
  165549. 10581N
  165550. 2/28/96V\A REVIEW. JOULE, JOHN A. THIANTHRENES. 1990, 48, 301 393. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165551. GABRIEL WEATHERHEAD
  165552. 10582N
  165553. 2/28/96V
  165554. A REVIEW. ELNAGDI, MOHAMED HILMY; ELMOGHAYER, MOHAMED RIFAAT HAMZA  SADEK, KAMAL USEF. CHEMISTRY OF PYRAZOLES CONDENSED TO HETEROAROMATIC FIVE  AND SIX MEMBERED RINGS. 1990, 48, 223 299. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165555. GABRIEL WEATHERHEAD
  165556. 10583N
  165557. 2/28/96
  165558. A REVIEW. BANNEMANN, H.; BRIJOUX, W. ORGANOCOBALT CATALYZED SYNTHESIS OF PYRIDINES. 1990, 48,177 222. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165559. GABRIEL WEATHERHEAD
  165560. 10584N
  165561. 2/28/96V
  165562. A REVIEW. CIRRINCIONE GIROLAMO, ALMERICO, ANNA MARIA; AIELLO, ENRICO; DATTOIO, GAETANO. DIAZOAZOLES. 1990, 48, 65 175. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165563. GABRIEL WEATHERHEAD
  165564. 10585N
  165565. 2/28/96V
  165566. A REVIEW. OAE, SHIGERU; FURUKAWA, NAOMICHI. HETEROAROMATIC SULFOXIDES AND SULFONES: LIGAND EXCHANGE AND COUPLING IN SULFURANES AND IPSO SUBSTITUTIONS. 1990, 48,1 61. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  165567. GABRIEL WEATHERHEAD
  165568. 10586N
  165569. 2/28/96V
  165570. A REVIEW. NOYORI, RYOJI; TAKAYA, HIDEMASA. BINAP: AN EFFICIENT CHIRAL ELEMENT FOR ASYMMETRIC CATALYSIS. 1990, 23(10), 345 50. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165571. GABRIEL WEATHERHEAD
  165572. 10587N
  165573. 2/28/96
  165574. A REVIEW. SAUVAGE, JEAN PIERRE. INTERLACING MOLECULAR THREADS ON TRANSITION METALS: CATENANDS, CATENATES, AND KNOTS. 1990, 23(10), 319 27. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165575. GABRIEL WEATHERHEAD
  165576. 10588N
  165577. 2/28/96V
  165578. A REVIEW. WALBORSKY, H. M. MECHANISM OF GRIGNARD REAGENT FORMATION. THE SURFACE NATURE OF THE REACTION. 1990, 23(9), 286 93. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165579. GABRIEL WEATHERHEAD
  165580. 10589N
  165581. 2/28/96V
  165582. A REVIEW. NIBBERING, NICO M. M. GAS PHASE ION/MOLECULE REACTIONS AS STUDIED BY FOURIER TRANSFORM ION CYCLOTRON RESONANCE. 1990, 23(9), 279 85. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165583. GABRIEL WEATHERHEAD
  165584. 10590N
  165585. 2/28/96V
  165586. A REVIEW. TIDWELL, THOMAS T. KETENE CHEMISTRY: THE SECOND GOLDEN AGE. 1990, 23(9), 273 9. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165587. GABRIEL WEATHERHEAD
  165588. 10591N
  165589. 2/28/96
  165590. A REVIEW. THEOPOLD, KLAUS H. ORGANOCHROMIUM(LII) CHEMISTRY: A NEGLECTED OXIDATION STATE. 1990, 23(8), 263 70. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165591. GABRIEL WEATHERHEAD
  165592. 10592N
  165593. 2/28/96V
  165594. A REVIEW. INGOLD, K. U.; LUSZTYK, J.; RANER, K. D. THE UNUSUAL AND THE UNEXPECTED IN AN OLD REACTION. THE PHOTOCHLORINATION OF ALKANES WITH MOLECULAR CHLORINE IN SOLUTION. 1990, 23(7), 219 25. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165595. GABRIEL WEATHERHEAD
  165596. 10593N
  165597. 2/28/96V
  165598. A REVIEW. SCHULTZ, ARTHUR G. ENANTIOSELECTIVE METHODS FOR CHIRAL CYCLOHEXANE RING SYNTHESIS. 1990 23(7), 207 13. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  165599. GABRIEL WEATHERHEAD
  165600. 10594N
  165601. 2/28/96V
  165602. A REVIEW. RAPPOPORT, ZVI, ED. THE CHEMISTRY OF ENOLS (THE CHEMISTRY OF FUNCTIONAL GROUPS). WILEY: CHICHESTER, U.K., 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165603. GABRIEL WEATHERHEAD
  165604. 10595N
  165605. 2/28/96
  165606. A REVIEW. POSPISIL, JAN  KLEMCHUK, PETER P. EDS. OXIDATION INHIBITION IN ORGANIC MATERIALS, VOLS. I AND 2. CRC PRESS: BOCA RATON, FL 1989. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165607. GABRIEL WEATHERHEAD
  165608. 10596N
  165609. 2/28/96V
  165610. A REVIEW. POPL, MILAN: FAEHNRICH, JAN; TATAR, VLASTIMIL. CHROMATOGRAPHIC ANALYSIS OF ALKALOIDS (CHROMATOGRAPHIC SCIENCE SERIES, VOL. 53). DEKKER: NEW YORK, 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165611. GABRIEL WEATHERHEAD
  165612. 10597N
  165613. 2/28/96V
  165614. A REVIEW. PLATZ, MATTHEW S., ED. KINETICS AND GPECTROSCOPY OF CARBENES AND BIRADICALS. PLENUM: NEW YORK, 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165615. GABRIEL WEATHERHEAD
  165616. 10598N
  165617. 2/28/96
  165618. A REVIEW. MACKIE, R. K., SMITH, D. M.; AITKEN, R. A. GUIDEBOOK TO ORGANIC SYNTHESIS. WILEY: CHICHESTER U.K., 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165619. GABRIEL WEATHERHEAD
  165620. 10599N
  165621. 2/28/96
  165622.  A REVIEW. LEFFLER, JOHN. E.; GRUNWALD, ERNEST. RATES AND EQUILIBRIA OF ORGANIC REACTIONS. AS TREATED BY STATISTICAL, THERMODYNAMIC, AND EXTRATHERMODYNAMIC METHODS. DOVER PUBLICATIONS: NEW YORK, 1989. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.
  165623. GABRIEL WEATHERHEAD
  165624. 10600N
  165625. 2/28/96
  165626. "A REVIEW. JACOB, JUERGEN. SULFUR ANALOGS OF POLYCYCLIC AROMATIC HYDROCARBONS (THIAARENES. ENVIRONMENTAL OCCURRENCE, CHEMICAL AND BIOLOGICAL PROPERTIES. CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, U.K. 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.
  165627. GABRIEL WEATHERHEAD
  165628. 10601N
  165629. 2/28/96
  165630. A REVIEW. JONES, GURNOS; GREENHILL, JOHN V., EDS. QUINOLINES. PART III. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 32). WILEY: NEW YORK, 1990.a
  165631. GABRIEL WEATHERHEAD
  165632. 10602N
  165633. 2/28/96V
  165634. A REVIEW. BENNINGA, H., A HISTORY OF LACTIC ACID MAKING. A CHAPTER IN THE HISTORY OF BIOTECHNOLOGY. KLUWER: DORDRECHT, NETHERLANDS, 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165635. GABRIEL WEATHERHEAD
  165636. 10603N
  165637. 2/28/96V
  165638. A REVIEW. BAILEY, P. D. AN INTRODUCTION TO PEPTIDE CHEMISTRY, WILEY: NEW YORK, 1990. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165639. GABRIEL WEATHERHEAD
  165640. 10604N
  165641. 2/28/96V
  165642. A REVIEW. KIM, YONG HAE, KIM, KYOUNG SOO. ACTIVATION OF SUPEROXIDE: ORGANIC SYNTHESIS USING PEROXYSULFUR INTERMEDIATES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165643. GABRIEL WEATHERHEAD
  165644. 10605
  165645. 2/28/96V
  165646. A REVIEW. VORONKOV, MIKHAIL, G.; DERYAGINA, ELEONORA N. THERMAL REACTIONS OF THIYL RADICALS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165647. GABRIEL WEATHERHEAD
  165648. 10606N
  165649. 2/28/96V
  165650. A REVIEW. YOKOYAMA, MASATAKA, TOGO, HIDEO. SYNTHESIS OF HETEROCYCLES VIA NOVEL REARRANGEMENT. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165651. GABRIEL WEATHERHEAD
  165652. 10607N
  165653. 2/28/96V
  165654. A REVIEW. MIURA, YOZO. SYNTHESES AND CHEMICAL BEHAVIORS OF PERSISTENT THIOAMINYL AND RELATED RADICALS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165655. GABRIEL WEATHERHEAD
  165656. 10608N
  165657. 2/28/96V
  165658. A REVIEW. SATO, RYU. REACTIONS OF ELEMENTAL SULFUR ACTIVATED BY AMMONIA OR AMINES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165659. GABRIEL WEATHERHEAD
  165660. 10609N
  165661. 2/28/96
  165662. A REVIEW. KATRITZKY, ALAN R.; SAVAGE, PAUL G. NEW SENSOR COATINGS FOR THE DETECTION OF ATMOSPHERIC CONTAMINANTS AND WATER. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165663. GABRIEL WEATHERHEAD
  165664. 10610N
  165665. 2/28/96V
  165666. A REVIEW. NAKAYAMA, JUZO; AKIMOTO KEIICHI; HOSHINO, MASAMATSU. SOME SYNTHETICALLY USEFUL REACTIONS OF ELEMENTAL SULFUR AND SELENIUM. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165667. GABRIEL WEATHERHEAD
  165668. 10611N
  165669. 2/28/96V
  165670. A REVIEW. ISHII, YASUTAKA, OGAWA, MASAYA. HYDROGEN PEROXIDE OXIDATION CATALYZED BY HETEROPOLY ACIDS COMBINED WITH CETYLPYRIDINIUM CHLORIDE. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165671. GABRIEL WEATHERHEAD
  165672. 10612N
  165673. 2/28/96
  165674. A REVIEW. UEMURA, SAKAE. SYNTHETIC UTILITY OF MCPBA OXIDATION OF ALKYL PHENYL SELENIDES AND TELLURIDES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165675. GABRIEL WEATHERHEAD
  165676. 10613N
  165677. 2/28/96V
  165678. A REVIEW. IMAMOTO, TSUNEO. NEW SYNTHETIC METHODS WITH LANTHANIDES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165679. GABRIEL WEATHERHEAD
  165680. 10614N
  165681. 2/28/96V
  165682. A REVIEW. INANAGA, JUNJI. REDUCTION OF ORGANIC FUNCTIONS VIA SMI2 PROMOTED ELECTRON TRANSFER PROCESS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165683. GABRIEL WEATHERHEAD
  165684. 10615N
  165685. 2/28/96V
  165686. A REVIEW. QUIN, LOUIS D. UNUSUAL PROPERTIES OF PHOSPHORUS FUNCTIONS IN THE 7 PHOSPHANORBORNENE RING SYSTEM. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165687. GABRIEL WEATHERHEAD
  165688. 10616N
  165689. 2/28/96
  165690. A REVIEW. CAMINADE, ANNE MARIE; MAJORAL, JEAN PIERRE. NEW ROUTES TO PHOSPHORUS THREE  AND FOUR MEMBERED RING. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165691. GABRIEL WEATHERHEAD
  165692. 10617N
  165693. 2/28/96V
  165694. A REVIEW. ARBUZOV, B. A., NIKONOV, G. N. P,B CONTAINING HETEROCYCLES WITH P
  165695. C O B, P C=C O B, P
  165696. B AND P
  165697. B FRAGMENTS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 3 SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN 1990.a
  165698. GABRIEL WEATHERHEAD
  165699. 10618N
  165700. 2/28/96V
  165701. A REVIEW. GRIBBLE, GORDON, W. SYNTHESIS AND ANTITUMOR ACTIVITY OF THE ELLIPTICINE ALKALOIDS AND RELATED COMPOUNDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165702. GABRIEL WEATHERHEAD
  165703. 10619N
  165704. 2/28/96V
  165705. A REVIEW. BLECHERT, SIEGFRIED; GUENARD, DANIEL. TAXUS ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.
  165706. GABRIEL WEATHERHEAD
  165707. 10620N
  165708. 2/28/96V
  165709. A REVIEW. HASHIMOTO, YOHEI; KAWANISHI, KAZUKO; ICHIMNRU, MOMOYO, HISTOCHEMISTRY OF ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165710. GABRIEL WEATHERHEAD
  165711. 10621N
  165712. 2/28/96V
  165713. A REVIEW. CROMBIE, L.; CROMBIE, W. M. L.; WHITING, D. A. THE ALKALOIDS OF KHAT (CATHA EDULIS). THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165714. GABRIEL WEATHERHEAD
  165715. 10622N
  165716. 2/28/96V
  165717. A REVIEW. CASTEDO, LUIS, TOJO, GABRIEL. PHENANTHRENE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165718. GABRIEL WEATHERHEAD
  165719. 10623N
  165720. 2/28/96V
  165721. A REVIEW. ROSS, W. BENZODIAZEPINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165722. GABRIEL WEATHERHEAD
  165723. 10624N
  165724. 2/28/96V
  165725. A REVIEW. STEGLICH, WOLFGANG; STRACK, DIETER. BETALAINS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 39, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165726. GABRIEL WEATHERHEAD
  165727. 10625N
  165728. 2/28/96V
  165729. A REVIEW. ATTA UR RAHMAN; CHOUDHARY, MUHAMMAD IQBAL. PURINE ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 38, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165730. GABRIEL WEATHERHEAD
  165731. 10626N
  165732. 2/28/96V
  165733. A REVIEW. BLASKO, DABOR. SPIROBENZYLISOQUINOLINE AND RELATED ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 38, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165734. GABRIEL WEATHERHEAD
  165735. 10627N
  165736. 2/28/96V
  165737. A REVIEW. NINOMIYA ICHIYA; KIGUCHI, TOSHIKO. ERGOT ALKALOIDS. THE ALKALOIDS. CHEMISTRY AND PHARMACOLOGY. VOLUME 38, A. BROSSI, ED., ACADEMIC PRESS: NEW YORK, 1990.a
  165738. GABRIEL WEATHERHEAD
  165739. 10628N
  165740. 2/28/96
  165741. MA REVIEW. PAINTER, GEORGE R.; SHOCKOR, JOHN P., ANDREWS, C. WEBSTER. APPLICATION OF MOLECULAR MECHANICS TO THE STUDY OF DRUG MEMBRANE INTERACTIONS: THE ROLE OF MOLECULAR CONFORMATION IN THE PASSIVE MEMBRANE PERMEABILITY OF ZIDOVUDINE (AZT). ADVANCES IN MOLECULAR MODELING. VOLUME 2 DENNIS LIOTTA, ED., JAI PRESS: GREENWICH, CT, 1990.
  165742. GABRIEL WEATHERHEAD
  165743. 10629N
  165744. 2/28/96V
  165745. A REVIEW. DURKIN, KATHLEEN, A.; SHERROD, MICHAEL J.; LIOTTA, DENNIS. EMPIRICAL DERIVATION OF MOLECULAR MECHANICS PARAMETER SETS: APPLICATION TO LACTAMS. ADVANCES IN MOLECULAR MODELING. VOLUME 2 DENNIS LIOTTA, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165746. GABRIEL WEATHERHEAD
  165747. 10630N
  165748. 2/28/96V
  165749. A REVIEW. GAJEWSKI, JOSEPH J.; GILBERT, KEVIN E.; MCKELVEY, JOHN. MMX. AN ENHANCED VERSION OF MM2. ADVANCES IN MOLECULAR MODELING. VOLUME 2 DENNIS LIOTTA, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165750. GABRIEL WEATHERHEAD
  165751. 10631N
  165752. 2/28/96
  165753. A REVIEW. DANNENBERG, J. J. THE MOLECULAR ORBITAL MODELING OF FREE RADICAL AND DIELS ALDER REACTIONS. ADVANCES IN MOLECULAR MODELING. VOLUME 2 DENNIS LIOTTA, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165754. GABRIEL WEATHERHEAD
  165755. 10632N
  165756. 2/28/96VeA REVIEW. DANNENBERG, J. J. THE MOLECULAR ORBITAL MODELING OF FREE RADICAL AND DIELS ALDER REACTIONS.a
  165757. GABRIEL WEATHERHEAD
  165758. 10633N
  165759. 2/28/96V
  165760. A REVIEW. DONALDSON, WILLIAM A. PALLADIUM MEDIATED METHYLENECYCLOPROPANE RING OPENING: APPLICATIONS TO ORGANIC SYNTHESIS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.a
  165761. GABRIEL WEATHERHEAD
  165762. 10634N
  165763. 2/28/96
  165764. A REVIEW. CROWE, WILLIAM E.; SCHREIBER, STUART L. P BOND HYBRIDIZATION IN TRANSITION METAL COMPLEXES: A STEREOELECTRONIC MODEL FOR CONFORMATIONAL ANALYSIS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.
  165765. GABRIEL WEATHERHEAD
  165766. 10635N
  165767. 2/28/96V
  165768. A REVIEW. UEMURA, MOTOKAZU. TRICARBONYL (H6 ARENE)CHROMIUM COMPLEXES IN ORGANIC SYNTHESIS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.a
  165769. GABRIEL WEATHERHEAD
  165770. 10636N
  165771. 2/28/96V
  165772. A REVIEW. HELQUIST, PAUL. DEVELOPMENT OF CARBENE COMPLEXES OF IRON AS NEW REAGENTS FOR SYNTHETIC ORGANIC CHEMISTRY. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.a
  165773. GABRIEL WEATHERHEAD
  165774. 10637N
  165775. 2/28/96
  165776. 1A REVIEW. OSHIMA, KOICHIORO. TRANSITION METAL CATALYZED SILYLMETALLATION OF ACETYLENES AND ET3B INDUCED RADICAL ADDITION OF PH3SNH TO ACETYLENES
  165777. SELECTIVE SYNTHESIS OF VINYLSILANES AND VINYLSTANNANES. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.
  165778. GABRIEL WEATHERHEAD
  165779. 10638N
  165780. 2/28/96
  165781. A REVIEW. DAVES, G. DOYLE, JR. PALLADIUM MEDIATED ARYLATION OF ENOL ETHERS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.a
  165782. GABRIEL WEATHERHEAD
  165783. 10639N
  165784. 2/28/96V
  165785. A REVIEW. COOTE, STEVEN, J.; DAVIES, STEPHEN G.; GOODFELLOW, CRAIG, L. SYNTHETIC APPLICATIONS OF CHROMIUM TRICARBONYL STABILIZED BENZYLIC CARBANIONS. ADVANCES IN METAL ORGANIC CHEMISTRY. VOLUME 2, LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CT, 1991.a
  165786. GABRIEL WEATHERHEAD
  165787. 10640N
  165788. 2/28/96V
  165789. A REVIEW. JANZEN, EDWARD G.; HAIRE, D. LARRY. TWO DECADES OF SPIN TRAPPING. ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165790. GABRIEL WEATHERHEAD
  165791. 10641N
  165792. 2/28/96
  165793. A REVIEW. ROSSI, ROBERTO A.; PIERINI, ADRIANA B.; PALACIOS, SARA M. NUCLEOPHILIC SUBSTITUTION BY THE SRN1 MECHANISM ON ALKYL HALIDES. ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165794. GABRIEL WEATHERHEAD
  165795. 10642N
  165796. 2/28/96V
  165797. A REVIEW. WAYNER, DANIEL D. M.; GRILLER, DAVID. FREE RADICAL THERMOCHEMISTRY. ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165798. GABRIEL WEATHERHEAD
  165799. 10643N
  165800. 2/28/96V
  165801. A REVIEW. CURRAN, DENNIS P. TANDEM RADICAL CYCLIZATIONS: A GENERAL STRATEGY FOR THE SYNTHESIS OF TRIQUINANE SESQUITERPENES. ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165802. GABRIEL WEATHERHEAD
  165803. 10644N
  165804. 2/28/96
  165805. A REVIEW. KOCHI, J. K. RADICAL CATIONS AS REACTIVE INTERMEDIATES IN AROMATIC ACTIVATION. ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165806. GABRIEL WEATHERHEAD
  165807. 10645N
  165808. 2/28/96V
  165809. A REVIEW. RUSSELL, GLEN, A. FREE RADICAL REACTIONS INVOLVING SATURATED AND UNSATURATED ALKYLMERCURIALS ADVANCES IN FREE RADICAL CHEMISTRY. VOLUME 1 DENNIS D. TANNER, ED., JAI PRESS: GREENWICH, CT, 1990.a
  165810. GABRIEL WEATHERHEAD
  165811. 10646N
  165812. 2/28/96V
  165813. A REVIEW. LOPEZ, L. PHOTOINDUCED ELECTRON TRANSFER OXYGENATIONS. 1990,156 (PHOTOINDUCED ELECTRON TRANSFER I), 117 166. TOPICS IN CURRENT CHEMISTRYa
  165814. GABRIEL WEATHERHEAD
  165815. 10647N
  165816. 2/28/96V
  165817. A REVIEW. KROGH, E.; WAN, P. PHOTOINDUCED ELECTRON TRANSFER OF CARBANIONS AND CARBOCATIONS. 1990, 156 (PHOTOINDUCED ELECTRON TRANSFER I), 93 116. TOPICS IN CURRENT CHEMISTRYa
  165818. GABRIEL WEATHERHEAD
  165819. 10648N
  165820. 2/28/96
  165821. A REVIEW. SAEVA, F. D. PHOTOINDUCED ELECTRON TRANSFER (PET) BOND CLEAVAGE REACTIONS. 1990, 156 (PHOTOINDUCED ELECTRON TRANSFER I), 59 62. TOPICS IN CURRENT CHEMISTRYa
  165822. GABRIEL WEATHERHEAD
  165823. 10649N
  165824. 2/28/96V
  165825. A REVIEW. ROTH, H. D. A BRIEF HISTORY OF PHOTOINDUCED ELECTRON TRANSFER AND RELATED REACTIONS. 1990, 156 (PHOTOINDUCED ELECTRON TRANSFER I), 1 19. TOPICS IN CURRENT CHEMISTRYa
  165826. GABRIEL WEATHERHEAD
  165827. 10650N
  165828. 2/28/96V
  165829. A REVIEW. HO, T. L. THROUGH BOND MODULATION OF REACTION CENTERS BY REMOTE SUBSTITUENTS. 1990, 155 (SMALL RING COMPOUNDS IN ORGANIC SYNTHESIS IV), 81 158. TOPICS IN CURRENT CHEMISTRYa
  165830. GABRIEL WEATHERHEAD
  165831. 10651N
  165832. 2/28/96V
  165833. A REVIEW. KOSTIKOV, R. R.; MOLCHANOV, A. P.; HOPF, H. GEM DIHALOCYCLOPROPANES IN ORGANIC SYNTHESIS. 1990 155 (SMALL RING COMPOUNDS IN ORGANIC SYNTHESIS IV), 4L 80. TOPICS IN CURRENT CHEMISTRYa
  165834. GABRIEL WEATHERHEAD
  165835. 10652N
  165836. 2/28/96
  165837. A REVIEW. KUWAJIMA, I., NAKAMURA, E. METAL HOMOENOLATES FROM SILOXYCYCLOPROPANES. 1990,155 (SMALL RING COMPOUNDS IN ORGANIC SYNTHESIS IV), 1 39. TOPICS IN CURRENT CHEMISTRYa
  165838. GABRIEL WEATHERHEAD
  165839. 10653N
  165840. 2/28/96V
  165841. A REVIEW. LUEF, WOLFGANG; KEESE, REINHART. STRAINED OLEFINS: STRUCTURE AND REACTIVITY OF NONPLANAR CARBON CARBON DOUBLE BONDS. 1991, 20, 231 318. TOPICS IN STEREOCHEMISTRYa
  165842. GABRIEL WEATHERHEAD
  165843. 10654N
  165844. 2/28/96V
  165845. A REVIEW. ZEFIROV, NIKOLAI S.; PALYULIN, VLADMMIR. CONFORMATIONAL ANALYSIS OF BICYCLO[3.3.1]NONANES AND THEIR HETERO ANALOGS. 1991, 20, 171 230. TOPICS IN STEREOCHEMISTRYa
  165846. GABRIEL WEATHERHEAD
  165847. 10655N
  165848. 2/28/96V
  165849. A REVIEW. OARE, DAVID C.; HEATHCOCK, CLAYTON, H. ACYCLIC STEREOCONTROL IN MICHAEL ADDITION REACTIONS OF ENAMINES AND ENOL ETHERS. 1991 20, 87 170 TOPICS IN STEREOCHEMISTRYa
  165850. GABRIEL WEATHERHEAD
  165851. 10656N
  165852. 2/28/96
  165853. A REVIEW. RIPKA, WILLIAM C.; BLANEY, JEFFREY M. COMPUTER GRAPHICS AND MOLECULAR MODELING IN THE ANALYSIS OF SYNTHETIC TARGETS. 1991 20, 1 85. TOPICS IN STEREOCHEMISTRYa
  165854. GABRIEL WEATHERHEAD
  165855. 10657N
  165856. 2/28/96V`A REVIEW. SIMPKINS, NIGEL S. THE CHEMISTRY OF VINYL SULFONES. 1990, 46(20), 6951 84. TETRAHEDRONa
  165857. GABRIEL WEATHERHEAD
  165858. 10658N
  165859. 2/28/96V
  165860. A REVIEW. ZHU, LIMING; TEDFORD, M. CATRIONA. APPLICATIONS OF PIG LIVER ESTERASES (PLE) IN ASYMMETRIC SYNTHESIS. 1990, 46(19), 6587 611. TETRAHEDRONa
  165861. GABRIEL WEATHERHEAD
  165862. 10659N
  165863. 2/28/96V
  165864. A REVIEW. CHANON, M., RAJZMANN, M. CHANON, F. ONE ELECTRON MORE, ONE ELECTRON LESS. WHAT DOES IT CHANGE? ACTIVATIONS INDUCED BY ELECTRON TRANSFER. THE ELECTRON, AN ACTIVATING MESSENGER. 1990, 46(18), 6193 299. TETRAHEDRONa
  165865. GABRIEL WEATHERHEAD
  165866. 10660N
  165867. 2/28/96VhA REVIEW. OKAMOTO, KAORU; GOTO, TOSHIO. GLYCOSIDATION OF SIALIC ACID. 1990, 46(17), 5835 57. TETRAHEDRON
  165868. GABRIEL WEATHERHEAD
  165869. 10661N
  165870. 2/28/96V
  165871. A REVIEW. JUNJAPPA, H.; ILA, H.; ASOKAN, C. V. A OXOKETENE S,S N,S  AND N,N ACETALS: VERSATILE INTERMEDIATES IN ORGANIC SYNTHESIS. 1990, 46(16), 5423 506. TETRAHEDRONa
  165872. GABRIEL WEATHERHEAD
  165873. 10662N
  165874. 2/28/96VYA REVIEW. WARD, R. S. ASYMMETRIC SYNTHESIS OF LIGNANS. 1990, 46(15), 5029 41. TETRAHEDRONa
  165875. GABRIEL WEATHERHEAD
  165876. 10663N
  165877. 2/28/96
  165878. ?A REVIEW. ROMO, DANIEL; ROMINE, JEFFREY, L.; MIDURA, WANDA; MEYERS, A. I. DIASTEREOSELECTIVE CYCLOPROPANATIONS OF CHIRAL BICYCLIC LACTAMS LEADING TO ENANTIOMERICALLY PURE CYCLOPROPANES. APPLICATION TO THE TOTAL SYNTHESIS OF CIS(LS,3R) DELTAMETHRINIC ACID AND R ( )DICTYOPTERENE C'. 1990, 46(13 14), 4951 94. TETRAHEDRON
  165879. GABRIEL WEATHERHEAD
  165880. 10664N
  165881. 2/28/96VrA REVIEW. LAMARE, VERONIQUE; FURSTOSS, ROLAND. BIOCONVERSION OF SESQUITERPENES. 1990, 46(12), 4109 32. TETRAHEDRONa
  165882. GABRIEL WEATHERHEAD
  165883. 10665N
  165884. 2/28/96VmA REVIEW. SARKAR, TARUN K. METHODS FOR THE SYNTHESIS OF ALLYLSILANES. PART 2. 1990, (12),1101 1111. SYNTHESISa
  165885. GABRIEL WEATHERHEAD
  165886. 10666N
  165887. 2/28/96VkA REVIEW. SARKAR, TARUN K. METHODS FOR THE SYNTHESIS OF ALLYLSILANES. PART 1. 1990, (11), 969 83. SYNTHESISa
  165888. GABRIEL WEATHERHEAD
  165889. 10667N
  165890. 2/28/96V
  165891. A REVIEW. TIDWELL, THOMAS T. OXIDATION OF ALCOHOLS BY ACTIVATED DIMETHYL SULFOXIDE AND RELATED REACTIONS: AN UPDATE. 1990, (10), 857 70. SYNTHESISa
  165892. GABRIEL WEATHERHEAD
  165893. 10668N
  165894. 2/28/96VbA REVIEW. CAMPAIGNE, E. ADVENTURES IN ORGANIC SULFUR CHEMISTRY. 1990, 10(1), 49 99. SULFUR REPORTSa
  165895. GABRIEL WEATHERHEAD
  165896. 10669N
  165897. 2/28/96V
  165898. A REVIEW. YOKOYAMA, MASATAKA; TOGO, HIDEO; KONDO, SHINICHI. SYNTHESIS OF HETEROCYCLES FROM KETENE DITHIOACETALS. 1990, 10(1), 23 47. SULFUR REPORTSa
  165899. GABRIEL WEATHERHEAD
  165900. 10670N
  165901. 2/28/96
  165902. A REVIEW. SADEKOV, I. D.; MAKSIMENKO, A. A.; MINKIN, V. I. PECULIARITIES IN THE REACTIVITY OF TELLURIUM ORGANIC COMPOUNDS IN COMPARISON WITH THEIR SULFUR AND SELENIUM ANALOGS. 1990, 9(5), 359 91. SULFUR REPORTSa
  165903. GABRIEL WEATHERHEAD
  165904. 10671N
  165905. 2/28/96V
  165906. A REVIEW. TEUBER, LENE. NATURALLY OCCURRING 1,2 DITHIOLANES AND 1,2,3 TRITHIANES. CHEMICAL AND BIOLOGICAL PROPERTIES. 1990, 9(4), 267 349. SULFUR REPORTSa
  165907. GABRIEL WEATHERHEAD
  165908. 10672N
  165909. 2/28/96V
  165910. A REVIEW. NOYORI, RYOJI. CHIRAL METAL COMPLEXES AS DISCRIMINATING MOLECULAR CATALYSTS. 1990, 248(4960), 1194 9; 1990, 249(4971), 844. SCIENCE (WASHINGTON, D.C. 1883 )a
  165911. GABRIEL WEATHERHEAD
  165912. 10673N
  165913. 2/28/96V
  165914. A REVIEW. RIEKE, REUBEN, D. PREPARTION OF ORGANOMETALLIC COMPOUNDS FROM HIGHLY REACTIVE METAL POWDERS. 1989, 246(4935), 1260 4. SCIENCE (WASHINGTON, D.C. 1883 )a
  165915. GABRIEL WEATHERHEAD
  165916. 10674N
  165917. 2/28/96
  165918. 6VyA REVIEW. KOVAL', I. V. ADVANCES M THE CHEMISTRY OF SULPHENIC ACID AMIDES. 1990, 59(4), 396 403. RUSSIAN CHEMICAL REVIEWSa
  165919. GABRIEL WEATHERHEAD
  165920. 10675N
  165921. 2/28/96V
  165922. A REVIEW. USOV, V. A.; TIMOKHINA, L. V.; VORONOV, M. G. THE SYNTHESIS AND PROPERTIES OF THIOALDEHYDES. 1990, 59(4), 378 395. RUSSIAN CHEMICAL REVIEWSa
  165923. GABRIEL WEATHERHEAD
  165924. 10676N
  165925. 2/28/96V
  165926. A REVIEW. TIMOFEEVA, T. V.; STRUCHKOV, YU, T. THE CONFORMATIONAL ANALYSIS OF ORGANOELEMENTAL AND ORGANOMETALLIC MOLECULES. 1990, 59(4), 320 343. RUSSIAN CHEMICAL REVIEWSa
  165927. GABRIEL WEATHERHEAD
  165928. 10677N
  165929. 2/28/96V
  165930. A REVIEW. BUCHACHENKO, A. L. ORGANIC AND MOLECULAR FERROMAGNETICS; ADVANCES AND PROBLEMS. 1990, 59(4), 307 319. RUSSIAN CHEMICAL REVIEWSa
  165931. GABRIEL WEATHERHEAD
  165932. 10678N
  165933. 2/28/96
  165934. A REVIEW. KRON, T. E.; TSVETKOV, E. N. NEUTRAL ACYCLIC ANALOGUES OF CROWN ETHERS AND CRYPTANDS AND THEIR COMPLEX FORMING PROPERTIES. 1990, 59(3), 283 298. RUSSIAN CHEMICAL REVIEWS . A REVIEWa
  165935. GABRIEL WEATHERHEAD
  165936. 10679N
  165937. 2/28/96V
  165938. A REVIEW. LAPACHEV, V. V.; PEBRENKO, 0. P.; MAMAEV, V. P. THE AZINYL AZINYLIDENE TAUTOMERISM OF AZINYLMETHANES AND GENERAL PROBLEMS OF THE TAUTOMERISM OF AZINES 1990, 59(3), 268 282 RUSSIAN CHEMICAL REVIEWSa
  165939. GABRIEL WEATHERHEAD
  165940. 10680N
  165941. 2/28/96V
  165942. A REVIEW. GAZIZOV, M. B.; KHAIRULLIN, R. A.; MOSKVA, V. V. REACTIONS OF PHOSPHORUS(III) CHLORIDES WITH CARBONYL COMPOUNDS. 1990, 59(3), 251 267. RUSSIAN CHEMICAL REVIEWSa
  165943. GABRIEL WEATHERHEAD
  165944. 10681N
  165945. 2/28/96V
  165946. A REVIEW. RAEVSKII, 0. A. THE STRUCTURE AND PROPERTIES OF COMPLEXES SIMULATING MOLECULAR RECOGNITION. 1990, 59(3), 219 33 RUSSIAN CHEMICAL REVIEWS . A REVIEWa
  165947. GABRIEL WEATHERHEAD
  165948. 10682N
  165949. 2/28/96
  165950. A REVIEW. TIMOKHIN, B. V. STRUCTURAL FEATURES AND REACTIVITY OF TETRAHALOMETHANES. 1990, 59(2), 193 203. RUSSIAN CHEMICAL REVIEWSa
  165951. GABRIEL WEATHERHEAD
  165952. 10683N
  165953. 2/28/96V
  165954. A REVIEW. MANUILOV, A. V.; BARKHASH, V. A. RECENT TRENDS IN THE THEORY OF THE DEAMINATION OF ALIPHATIC AND ALICYCLIC AMINES 1990, 59(2), 179 192. RUSSIAN CHEMICAL REVIEWSa
  165955. GABRIEL WEATHERHEAD
  165956. 10684N
  165957. 2/28/96VtA REVIEW. MALKIN, YA N.; KUZ'MIN, V. A. THE PHOTOCHEMISTRY OF AZINES. I990~ 59(2), 164 178. RUSSIAN CHEMICAL REVIEWSa
  165958. GABRIEL WEATHERHEAD
  165959. 10685N
  165960. 2/28/96VtA REVIEW. GORELIK, M. V. CURRENT STATE OF THE PROBLEM OF AROMATICITY. 1990, 59(2), 116 133. RUSSIAN CHEMICAL REVIEWSa
  165961. GABRIEL WEATHERHEAD
  165962. 10686N
  165963. 2/28/96V
  165964. A REVIEW. JIANG, ZHI QIN. NOVEL PATHWAYS IN ELECTRON TRANSFER PHOTOOXYGENATIONS. 1990, 14(2)7 185 207. RESEARCH ON CHEMICAL INTERMEDIATESa
  165965. GABRIEL WEATHERHEAD
  165966. 10687N
  165967. 2/28/96
  165968. A REVIEW. XIN, WEN JUAN; ZHAO, BAO LU; LI, XIAO JIE; HOU, JING WU. SCAVENGING EFFECTS OF CHINESE HERBS AND NATURAL HEALTH PRODUCTS ON ACTIVE OXYGEN RADICALS. 1990,14(2),171 83.  RESEARCH ON CHEMICAL INTERMEDIATESa
  165969. GABRIEL WEATHERHEAD
  165970. 10688N
  165971. 2/28/96V
  165972. A REVIEW. LEI, XUEGONG. REACTIONS OF TRIPLET BENZYL RADICAL PAIRS IN CONSTRAINED ENVIRONMENTS. 1990, 14(1),15 46.  RESEARCH ON CHEMICAL INTERMEDIATESa
  165973. GABRIEL WEATHERHEAD
  165974. 10689N
  165975. 2/28/96V
  165976. A REVIEW. SNIECKUS, V. THE DIRECTED ORTHO METALATION REACTION. METHODOLOGY, APPLICATIONS, SYNTHETIC LINKS, AND A NONAROMATIC RAMIFICATION. 1990, 62(10), 2047 56 PURE AND APPLIED CHEMISTRYa
  165977. GABRIEL WEATHERHEAD
  165978. 10690N
  165979. 2/28/96V
  165980. A REVIEW. SEREBRYAKOV, E. P.; NGUYEN CONG HAO; MAVROV, M. V. CHIRAL BUILDING BLOCKS BASED ON TECHNICAL GRADE B CITRONELLENE. 1990, 62(10), 2041 6. PURE AND APPLIED CHEMISTRYa
  165981. GABRIEL WEATHERHEAD
  165982. 10691N
  165983. 2/28/96
  165984. A REVIEW. SEMMELHACK, M. F.; KIM, CHUNG; ZHANG, NAN; BODUROW, C.; SANNER, M.; DOBLER, W.; MEIER, M. INTRAMOLECULAR ALKOXYCARBONYLATION OF HYDROXY ALKENES PROMOTED BY PALLADIUM(II). 1990, 62(10), 2035 40. PURE AND APPLIED CHEMISTRYa
  165985. GABRIEL WEATHERHEAD
  165986. 10692N
  165987. 2/28/96V
  165988. A REVIEW. LASZLO, PIERRE. CATALYSIS OF ORGANIC REACTIONS BY INORGANIC SOLIDS. 1990, 62(10), 2027 30. PURE AND APPLIED CHEMISTRYa
  165989. GABRIEL WEATHERHEAD
  165990. 10693N
  165991. 2/28/96
  165992. ;A REVIEW. ISOBE, MINORU; NISHIKAWA, TOSHIO; HERUNSALEE, ANGKANA; TSUKIYAMA, TAKAHIRO; HIROSE, YUMI; SHIMOKAWA, KENICHIROU; GOTO, TOSHIO. METHODOLOGY FOR STEREOCHEMICAL CONTROL IN BIOACTIVE NATURAL PRODUCT SYNTHESIS
  165993. NEW METHODS TOWARD ENEDIYNE ANTITUMOR ANTIBIOTICS. 1990, 62(10), 2007 12. PURE AND APPLIED CHEMISTRY
  165994. GABRIEL WEATHERHEAD
  165995. 10694N
  165996. 2/28/96
  165997. A REVIEW. FIANDANESE, VITO. SEQUENTIAL CROSS COUPLING REACTIONS AS A VERSATILE SYNTHETIC TOOL. 1990, 62(10),1987S92. PURE AND APPLIED CHEMISTRYa
  165998. GABRIEL WEATHERHEAD
  165999. 10695N
  166000. 2/28/96V
  166001. A REVIEW. BERGMAN, JAN; PELCMAN, BENJAMINA. SYNTHESIS OF CARBAZOLE ALKALOIDS. 1990, 62(10), 1967 76. PURE AND APPLIED CHEMISTRYa
  166002. GABRIEL WEATHERHEAD
  166003. 10696N
  166004. 2/28/96
  166005. (A REVIEW. JORGENSEN, WILLIAM L.; LAIRD, ELLEN R.; GUSHURST, ALAN J.; FLEISCHER, JAN M.; GOTHE, SCOTT A.; HELSON, HAROLD E.; PADERES, GENEVIEVE D.; SINCLAIR, SHENNA. CAMEO: A PROGRAM FOR THE LOGICAL PREDICTION OF THE PRODUCTS OF ORGANIC REACTIONS. 1990, 62(10), 1921 32. PURE AND APPLIED CHEMISTRY
  166006. GABRIEL WEATHERHEAD
  166007. 10697N
  166008. 2/28/96VwA REVIEW. SIMONS, J. P. STEREODYNAMICS OF MOLECULAR PHOTODISSOCIATION. 1990, 62(8), 1573 80. PURE AND APPLIED CHEMISTRYa
  166009. GABRIEL WEATHERHEAD
  166010. 10698N
  166011. 2/28/96
  166012. A REVIEW. SCALSNO J C.; WINTGENS, V.; NETTO FERREIRA, J. C. MECHANISTIC STUDIES OF THE PHOTOGENERATION AND PHOTO  CHEMISTRY OF ORTHO XYLYLENES. 1990, 62(8),1557 64. PURE AND APPLIED CHEMISTRYa
  166013. GABRIEL WEATHERHEAD
  166014. 10699N
  166015. 2/28/96V
  166016. A REVIEW. PERUTZ, ROBIN, N.; BELT, SIMON T.; MCCAMLEY, ANDREW; WHITTLESEY, MICHAEL K. CARBON HYDROGEN BOND ACTIVATION BY ORGANOMETALLICS: THE ROLE OF MATRIX ISOLATION STUDIES. PURE AND APPLIED CHEMISTRYa
  166017. GABRIEL WEATHERHEAD
  166018. 10700N
  166019. 2/28/96V
  166020. A REVIEW. MIYASHI, TSUTOMU; IKEDA, HIROSHI; KOMNO, AKMORI; OKITSU OSAMU; TAKAHASHI, YASUTAKE. PHOTOINDUCED ELECTRON TRANSFER REACTIONS OF THE COPE AND RELATED SYSTEMS. 1990, 62(8), 1531 8. PURE AND APPLIED CHEMISTRYa
  166021. GABRIEL WEATHERHEAD
  166022. 10701N
  166023. 2/28/96
  166024. A REVIEW. RANGANSTHAN, S. RANGANATHAN, D., BAMEZAI, S., SINGH, W. P., BHATTACHARYJA, D.; SINGH, G. P.; RATHI, R.; SAINI, S. JAYARAMSN, N.; PATEL, B. K. CHEMICAL APPROACHES TO THE RE STRUCTURING OF PROTEINS. 1990, 62(7),1437 40. PURE AND APPLIED CHEMISTRYa
  166025. GABRIEL WEATHERHEAD
  166026. 10702N
  166027. 2/28/96V
  166028. A REVIEW. ATTA UR RAHMAN  QURESHI, M. MUNAWER. APPLICATIONS OF MODERN 2D NMR TECHNIQUES IN STRUCTURE ELUCIDATION OF NATURAL PRODUCTS. 1990, 62(7), 1385 8. PURE AND APPLIED CHEMISTRYa
  166029. GABRIEL WEATHERHEAD
  166030. 10703N
  166031. 2/28/96V
  166032. A REVIEW. YADAV J. S., DESBPANDE, PRASSD K.  SHARMA, G. V. M. SYNTHESIS OF BIOLOGICALLY ACTIVE COMPOUNDS OF AGRICULTURAL INTEREST. 1990, 62(7),1333 8. PURE AND APPLIED CHEMISTRYa
  166033. GABRIEL WEATHERHEAD
  166034. 10704N
  166035. 2/28/96ViA REVIEW. KHRIPSCH, V. A. SYNTHESIS OF BRASSINOSTEROIDS. 1990, 62(7), 1319 24. PURE AND APPLIED CHEMISTRYa
  166036. GABRIEL WEATHERHEAD
  166037. 10705N
  166038. 2/28/96
  166039. A REVIEW. GURJAR, MUKUND, K. SYNTHESIS OF ENANTIOMERICALLY PURE COMPOUNDS OF BIOLOGICAL INTEREST. 1990, 62(7),1293 8. PURE AND APPLIED CHEMISTRYa
  166040. GABRIEL WEATHERHEAD
  166041. 10706N
  166042. 2/28/96V
  166043. A REVIEW. COREY, E. J. NEW ENANTIOSELECTIVE ROUTES TO BIOLOGICALLY INTERESTING COMPOUNDS. 1990, 62(7), 1209 16. PURE AND APPLIED CHEMISTRYa
  166044. GABRIEL WEATHERHEAD
  166045. 10707N
  166046. 2/28/96V
  166047. A REVIEW. DONDONI, ALESSANDRO. NEW ORGANOMETALLIC REAGENTS. USE OF 2 (TRIMETHYLSILYL)THIAZOLE IN ACYCLIC STEREOSELECTIVE STRATEGIES. 1990 62(4), 643 52. PURE AND APPLIED CHEMISTRYa
  166048. GABRIEL WEATHERHEAD
  166049. 10708N
  166050. 2/28/96V
  166051. A REVIEW. CHARTON MARVIN. THE QUANTITATIVE DESCRIPTION OF AMINO ACID, PEPTIDE AMD PROTEIN PROPERTIES AND BIOACTIVITIES. 1990, 18, 163 284. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  166052. GABRIEL WEATHERHEAD
  166053. 10709N
  166054. 2/28/96
  166055. A REVIEW. EMER, OTTO. PHYSICOCHEMICAL PRECONDITIONS OF LINEAR FREE ENERGY RELATIONSHIPS. 1990, 18,129 161. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  166056. GABRIEL WEATHERHEAD
  166057. 10710N
  166058. 2/28/96V
  166059. A REVIEW. ZELEWSKI, ROMUALD, 1. APPLICATION OF PRINCIPAL COMPONENT ANALYSIS IN ORGANIC CHEMISTRY. 1990, 18, 77 128. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  166060. GABRIEL WEATHERHEAD
  166061. 10711N
  166062. 2/28/96V
  166063. A REVIEW. HALDNA, U. ESTIMATION OF THE BASICITY CONSTANTS OF WEAK BASES BY THE TARGET TESTING METHOD OF FACTOR ANALYSIS. 1990, 18, 65 75. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  166064. GABRIEL WEATHERHEAD
  166065. 10712N
  166066. 2/28/96V
  166067. A REVIEW. DAHNE, SIEGFRIED  HOFFMANN, KATRIN. FREE ENERGY RELATIONSHIPS IN STRONGLY CONJUGATED SUBSTITUENTS: THE POLYMETHINE APPROACH. 1990, 18,1 64. PROGRESS IN PHYSICAL ORGANIC CHEMISTRYa
  166068. GABRIEL WEATHERHEAD
  166069. 10713N
  166070. 2/28/96
  166071. A REVIEW. BALLINI, R.; PETRINI, M.; MAROTTA, E.; RIGHI, P. RECENT PROGRESS IN THE SYNTHESIS AND REACTIVITY OF NITROKETONES. 1990, 22(6), 707 46. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166072. GABRIEL WEATHERHEAD
  166073. 10714N
  166074. 2/28/96V
  166075. A REVIEW. RZESZOTARSKA, BARBARA; MASIUKIEWICZ, ELZBIETA. ARGININE, HISTIDINE AND TRYPTOPHAN IN PEPTIDE SYNTHESIS. THE INDOLE FUNCTION OF TRYPTOPHAN. 1990, 22(6), 655 706. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166076. GABRIEL WEATHERHEAD
  166077. 10715N
  166078. 2/28/96V
  166079. A REVIEW. MAGNUSSON, G. REARRANGEMENTS OF EPOXY ALCOHOLS AND RELATED COMPOUNDS. 1990, 22(5), 547 574. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166080. GABRIEL WEATHERHEAD
  166081. 10716N
  166082. 2/28/96V
  166083. A REVIEW. JORDAN, RICHARD F., BRADLEY, PRUDENCE K., LAPOINTE, ROBERT E; TAYLOR, DENNIS F. CATIONIC ZIRCONIUM CATALYSTS FOR CARBON CARBON BOND FORMING CHEMISTRY. 1990, 14(6 7), 505 11. NEW JOURNAL OF CHEMISTRYa
  166084. GABRIEL WEATHERHEAD
  166085. 10717N
  166086. 2/28/96V
  166087. A REVIEW. CHIUSOLI, GIAM PAOLO; COSTA, MICRO; PELIZZI, CORRADO. SOME ASPECTS OF THE ORGANIC CHEMISTRY OF COBALT. 1990, 14(6 7), 465 9. NEW JOURNAL OF CHEMISTRYa
  166088. GABRIEL WEATHERHEAD
  166089. 10718N
  166090. 2/28/96V
  166091. A REVIEW. NORMANT,J.F. ORGANOBISMETALLIC REAGENTS. PREPARATION AND USE IN SYNTHESIS 1990, 14(6 7), 461 4. NEW JOURNAL OF CHEMISTRYa
  166092. GABRIEL WEATHERHEAD
  166093. 10719N
  166094. 2/28/96V
  166095. A REVIEW. KAGAN, H. B. DIVALENT SAMARIUM COMPOUNDS: PERSPECTIVES FOR ORGANIC CHEMISTRY. 1990, 14(6 7), 453 60. NEW JOURNAL OF CHEMISTRYa
  166096. GABRIEL WEATHERHEAD
  166097. 10720N
  166098. 2/28/96V
  166099. A REVIEW. BAECKVSLL, JAN E. STEREOSELECTIVE ANNULATIONS VIA PALLADIUM CATALYZED REACTIONS. 1990, 14(6 7), 447 52. NEW JOURNAL OF CHEMISTRYa
  166100. GABRIEL WEATHERHEAD
  166101. 10721N
  166102. 2/28/96V
  166103. A REVIEW. DOETZ, KARL HEINZ. CARBENE COMPLEXES IN STEREOSELECTIVE CYCLOADDITION REACTIONS. 1990, 14(6 7), 433 45. NEW JOURNAL OF CHEMISTRY
  166104. GABRIEL WEATHERHEAD
  166105. 10722N
  166106. 2/28/96V}A REVIEW. KAMAL, AHMED. RECENT ADVANCES IN THE SYNTHETIC USES OF CHLOROCARBONYL ISOCYANATE. 1990, 31(7),1377 91. HETEROCYCLESa
  166107. GABRIEL WEATHERHEAD
  166108. 10723N
  166109. 2/28/96V
  166110. A REVIEW. BOX, VERNON G. S. THE ROLE OF LONE PAIR INTERACTIONS IN THE CHEMISTRY OF THE MONOSACCHARIDES. THE ANOMERIC EFFECT. 1990, 31, 1157 HETEROCYCLESa
  166111. GABRIEL WEATHERHEAD
  166112. 10724N
  166113. 2/28/96V
  166114. A REVIEW. SELLERGREN, BOERJE. MOLECULAR IMPRINTING BY NONCOVALENT INTERACTIONS: TAILOR MADE CHIRAL STATIONARY PHASES OF HIGH SELECTIVITY AND SAMPLE LOAD CAPACITY. 1989, 1(1), 63 8. CHIRALITYa
  166115. GABRIEL WEATHERHEAD
  166116. 10725N
  166117. 2/28/96VnA REVIEW. MASON, STEPHEN F. THE DEVELOPMENT OF CONCEPTS OF CHIRAL DISCRIMINATION. 1989, 1(3), 183 91 CHIRALITYa
  166118. GABRIEL WEATHERHEAD
  166119. 10726N
  166120. 2/28/96
  166121. A REVIEW. LLOYD, DAVID K.; GOODALL, DAVID M. POLARIMETRIC DETECTION IN HIGH PERFORMANCE LIQUID CHROMATOGRAPHY. 1989, 1(4) 251 64. CHIRALITYa
  166122. GABRIEL WEATHERHEAD
  166123. 10727N
  166124. 2/28/96VQA REVIEW. GOLDING, BERNARD T. THE B12 MYSTERY. 1990, 26(10), CHEMISTRY IN BRITAINa
  166125. GABRIEL WEATHERHEAD
  166126. 10728N
  166127. 2/28/96VyA REVIEW. HOUNSELL, ELIZABETH F. SPECTROSCOPIC STUDIES OF COMPLEX CARBOHYDRATES. 1990, 26(7), 684 87 CHEMISTRY IN BRITAINa
  166128. GABRIEL WEATHERHEAD
  166129. 10729N
  166130. 2/28/96VwA REVIEW. BUCKE, C., RASTOLL, R. A. SYNTHESIZING SUGARS BY ENZYMES IN REVERSE. 1990, 26(7), 675 78 CHEMISTRY IN BRITAINa
  166131. GABRIEL WEATHERHEAD
  166132. 10730N
  166133. 2/28/96VjA REVIEW. GAREGG, J. ARTIFICIAL ANTIGENS PROSPECTS FOR MEDICINE. 1990, 26(7); 669 74. CHEMISTRY IN BRITAINa
  166134. GABRIEL WEATHERHEAD
  166135. 10731N
  166136. 2/28/96VqA REVIEW. ABEL, EDWARD. FLIP, FLOP, AND WHIZZ IN METAL SULFUR COMPLEXES. 1990, 26(2), 148 52 CHEMISTRY IN BRITAIN
  166137. GABRIEL WEATHERHEAD
  166138. 10732N
  166139. 2/28/96V
  166140. A REVIEW. KANG, ANGRAY, S.; KINGSBURY, GILLIAN A.; BLACKBURN, G. MICHAEL, BURTON, DENNIS R. CATALYTIC ANTIBODIES DESIGNER ENZYMES. 1990, 26(2), 128 32. CHEMISTRY IN BRITAINa
  166141. GABRIEL WEATHERHEAD
  166142. 10733N
  166143. 2/28/96VhA REVIEW. WRACKMEYER, BERND. MULTINUCLEAR NMR AND TIN CHEMISTRY. 1990, 26(1), 48 9. CHEMISTRY IN BRITAINa
  166144. GABRIEL WEATHERHEAD
  166145. 10734N
  166146. 2/28/96VRA REVIEW. KROTO, HAROLD. GIANT FULLERENES. 1990, 26(1), 40 2. CHEMISTRY IN BRITAINa
  166147. GABRIEL WEATHERHEAD
  166148. 10735N
  166149. 2/28/96ViA REVIEW. LEY, STEVEN V.; TOOGOOD, PETER L. INSECT ANTIFEEDANTS. 1990, 26(1), 31 35. CHEMISTRY IN BRITAINa
  166150. GABRIEL WEATHERHEAD
  166151. 10736N
  166152. 2/28/96V
  166153. A REVIEW. PAGE, PHILIP C. BULMAM; SUKHBMDER, S. KLAIR; ROSENTHAL, STEPHEN. SYNTHESIS AND CHEMISTRY OF ACYL SILANES. 1990 19(2), 147 195. CHEMICAL SOCIETY REVIEWSa
  166154. GABRIEL WEATHERHEAD
  166155. 10737
  166156. 2/28/96V
  166157. A REVIEW. IKCHOON, LEE. STEREOELECTRONIC ORIGINS OF THE INTRINSIC BARRIER TO SN2 REACTIONS. 1990, 19(2),133 145. CHEMICAL SOCIETY REVIEWSa
  166158. GABRIEL WEATHERHEAD
  166159. 10738N
  166160. 2/28/96V
  166161. A REVIEW. KATRITZKY, ALAN R.; BRYCKI, BOGUMIL E. THE MECHANISMS OF NUCLEOPHILIC SUBSTITUTION IN ALIPHATIC COMPOUNDS. 1990, 19(2), 83 105. CHEMICAL SOCIETY REVIEWSa
  166162. GABRIEL WEATHERHEAD
  166163. 10739N
  166164. 2/28/96V}A REVIEW. SCHWAB, JOHN M.; HENDERSON, BARRY S. ENZYME CATALYZED ALLYLIC REARRANGEMENTS. 1990, 90(7),1203 45. CHEMICAL REVIEWSa
  166165. GABRIEL WEATHERHEAD
  166166. 10740N
  166167. 2/28/96V
  166168. A REVIEW. SCHERER, OTTO J. COMPLEXES WITH SUBSTITUENT FREE ACYCLIC AND CYCLIC PHOSPHORUS, ARSENIC, ANTIMONY AND BISMUTH LIGANDS. 1990, 29(10),1104 22. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166169. GABRIEL WEATHERHEAD
  166170. 10741N
  166171. 2/28/96
  166172. A REVIEW. WERNER;HELMUT. COMPLEXES OF CARBON MONOXIDE AND ITS RELATIVES AN ORGANOMETALLIC FAMILY CELEBRATES ITS BIRTHDAY ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166173. GABRIEL WEATHERHEAD
  166174. 10742N
  166175. 2/28/96V
  166176. A REVIEW. VAN GUNSTEREN, WILFRED, F.; BERENDSEN, HERMAN J. C. COMPUTER SIMULATION OF MOLECULAR DYNAMICS. METHODOLOGY, APPLICATIONS AND PERSPECTIVES IN CHEMISTRY. 1990, 29(9), ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166177. GABRIEL WEATHERHEAD
  166178. 10743N
  166179. 2/28/96V
  166180. A REVIEW. BRINGMANN, GERHARD; WELTER, RAINER; WENIEB, ROLF. THE DIRECTED SYNTHESIS OF BIARYL COMPOUNDS: MODERN CONCEPTS AND STRATEGIES. 1990, 29(9), 977 91. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166181. GABRIEL WEATHERHEAD
  166182. 10744N
  166183. 2/28/96V
  166184. A REVIEW. SCHURIG, VOLKER, NOWOTNY, HANS PETER. GAS CHROMATOGRAPHIC SEPARATION OF ENANTIOMERS ON CYCLODEXTRIN DERIVATIVES. 1990, 29(9), 939 57. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  166185. GABRIEL WEATHERHEAD
  166186. 10745N
  166187. 2/28/96V
  166188. A REVIEW. LEDL, FRANZ; SCHLEICHER, ERWIN. NEW ASPECTS OF THE MAILLARD REACTION IN FOODS AND IN THE HUMAN BODY. 1990, 29(6) 565 94 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166189. GABRIEL WEATHERHEAD
  166190. 10746N
  166191. 2/28/96
  166192. A REVIEW. SHAMBAYATI, SOROOSH; CROWE, WILLIAM E.; SCHREIBER, STUART L. ON THE CONFORMATION AND STRUCTURE OF ORGANOMETAL COMPLEXES IN THE SOLID STATE: TWO STUDIES RELEVANT TO CHEMICAL SYNTHESIS. 1990, 29(3), 256 72. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  166193. GABRIEL WEATHERHEAD
  166194. 10747N
  166195. 2/28/96V
  166196. A REVIEW. HEATHCOCK, CLAYTON H. UNDERSTANDING AND CONTROLLING DIASTEREOFACIAL SELECTIVITY IN CARBON CARBON BOND FORMING REACTIONS. 1990, 23(4), 99 111. ALDRICHIMICA ACTAa
  166197. GABRIEL WEATHERHEAD
  166198. 10748N
  166199. 2/28/96VsA REVIEW. KORNBLUM, NATHAN. SYNTHETIC ASPECTS OF ELECTRON TRANSFER CHEMISTRY. 1990, 23(3), 71 78. ALDRICHIMICA ACTA
  166200. GABRIEL WEATHERHEAD
  166201. 10749N
  166202. 2/28/96VVA REVIEW. PRELOG, VLADIMIR. ALBERT ESCHENMOSER. 1990, 23(3), 59 .,4. ALDRICHIMICA ACTAa
  166203. GABRIEL WEATHERHEAD
  166204. 10750N
  166205. 2/28/96VWA REVIEW. KULKARNI YASHWAMT S. CARBOXYOLEFINATION. 1990,23(2), 39 41. ALDRICHIMICA ACTAa
  166206. GABRIEL WEATHERHEAD
  166207. 10751N
  166208. 2/28/96V
  166209. A REVIEW. DAVIES, STEPHEN G. THE CHIRAL AUXILIARY [(PH)FE(CO) (PPH3)] FOR ASYMMETRIC SYNTHESIS. 1990, 23(2), 31 37. ALDRICHIMICA ACTAa
  166210. GABRIEL WEATHERHEAD
  166211. 10752N
  166212. 2/28/96V
  166213. A REVIEW. GRIFFITH, WILLIAM P., LEY, STEPHEN V. TPAP: TETRA NPROPYLAMMONIUM PERRUTHENATE, A MILD AND CONVENIENT OXIDANT FOR ALCOHOLS. 1990, 23(1),13 19. ALDRICHIMICA ACTAa
  166214. GABRIEL WEATHERHEAD
  166215. 10753N
  166216. 2/28/96VgA REVIEW. BARTON, DEREK H. R. THE INVENTION OF CHEMICAL REACTIONS. 1990, 23(1), 3 10. ALDRICHIMICA ACTAa
  166217. GABRIEL WEATHERHEAD
  166218. 10754N
  166219. 2/28/96
  166220. A REVIEW. INGOLD, KEITH U. AT THE ORGANIC CHEMISTRY/BIOSCIENCE INTERFACE: RATE PROCESSES IN COMPLEX SYSTEMS. 1989, 22(3), 69 73. ALDRICHIMICA ACTAa
  166221. GABRIEL WEATHERHEAD
  166222. 10755N
  166223. 2/28/96V
  166224. A REVIEW. KNOWLES, JEREMY R. MECHANISTIC INGENUITY IN ENZYME CATALYSIS: DEHYDROQUINATE SYNTHASE. 1989, 22(3), 59~6. ALDRICHIMICA ACTAa
  166225. GABRIEL WEATHERHEAD
  166226. 10756N
  166227. 2/28/96VdA REVIEW. RUFFING, CHARLES J. RHODIUM CATALYZED HYDROBORATION. 1989, 22(3), 80 81. ALDRICHIMICA ACTAa
  166228. GABRIEL WEATHERHEAD
  166229. 10757N
  166230. 2/28/96V
  166231. A REVIEW. MASSEY, A. G.; HUMPHRIES, R. E. THE DIRECT SYNTHESIS OF NON TRANSITION METAL ORGANO DERIVATIVES 1989, 22(2), ALDRICHIMICA ACTAa
  166232. GABRIEL WEATHERHEAD
  166233. 10758N
  166234. 2/28/96V
  166235. A REVIEW. VEITH, M. ALKYL  AND ARYL SUBSTITUTED MAIN GROUP METAL AMIDES. 1990, 31, 269 300. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166236. GABRIEL WEATHERHEAD
  166237. 10759N
  166238. 2/28/96
  166239. A REVIEW. HUGHES, RUSSELL P. ORGANO TRANSITION METAL COMPOUNDS CONTAINING PERFLUORINATED LIGANDS. 1990, 31,183 267. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166240. GABRIEL WEATHERHEAD
  166241. 10760N
  166242. 2/28/96V
  166243. A REVIEW. ELLIS JOHN, E. HIGHLY REDUCED METAL CARBONYL ANIONS: SYNTHESIS, CHARACTERIZATION, AND CHEMICAL PROPERTIES. 1990, 31, 1 51. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166244. GABRIEL WEATHERHEAD
  166245. 10761N
  166246. 2/28/96V
  166247. A REVIEW. CHOJNOWSKI, JULIAN, STIMCZYK, WLODZMMIERZ. DISSOCIATIVE PATHWAYS IN SUBSTITUTION AT SILICON IN SOLUTION: SILICON CATIONS RSI+ RSI+   NU, AND SILENE TYPE SPECIES R2SI=X AS INTERMEDIATES. 1990, 30, 243 307. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166248. GABRIEL WEATHERHEAD
  166249. 10762N
  166250. 2/28/96V
  166251. A REVIEW. HOSMANE, NARAYAN S.; MAGUIRE, JOHN A. SYNTHESES, STRUCTURES, BONDING AND REACTIVITY OF MAIN GROUP HETERO  CARBORANES 1990, 30, 99 150.  ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166252. GABRIEL WEATHERHEAD
  166253. 10763
  166254. 2/28/96V
  166255. A REVIEW. ASHE, ARTHUR J., III. THERMOCHROMIC DISTIBINES AND DIBISMUTHINES. 1990, 30, 77 97. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166256. GABRIEL WEATHERHEAD
  166257. 10764N
  166258. 2/28/96V
  166259. A REVIEW. DAVIES, STEPHEN G., MCNALLY, JOHN P.; SMALLRIDGE, ANDREW J. CHEMISTRY OF THE CYCLOPENTADIENYL BISPHOSPHINE RUTHENIUM AUXILIARY. 1990, 30, 1 76. ADVANCES IN ORGANOMETALLIC CHEMISTRYa
  166260. GABRIEL WEATHERHEAD
  166261. 10765N
  166262. 2/28/96V
  166263. A REVIEW. TROFIMOV, BORIS A. PREPARATION OF PYRROLES FROM KETOXIMES AND ACETYLENES. 1990, 51,178 301. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166264. GABRIEL WEATHERHEAD
  166265. 10766N
  166266. 2/28/96V
  166267. A REVIEW. ACHESON, R. MORRIN. L HYDROXYPYRROLES, L HYDROXYINDOLES, AND 9 HYDROXYCARBAZOLES 1990, 51, 106 175. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166268. GABRIEL WEATHERHEAD
  166269. 10767N
  166270. 2/28/96
  166271. A REVIEW. MEZHETRITSKII, VALERII V.; TKACHENKO, VERA V. SYNTHESIS OF PERI ANNELATED HETEROCYCLIC SYSTEMS. 1990, 51, 2 103. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166272. GABRIEL WEATHERHEAD
  166273. 10768N
  166274. 2/28/96V
  166275. A REVIEW. BUSBY, REGINALD E. THIADIAZINES WITH ADJACENT SULFUR AND NITROGEN RING ATOMS. 1990, 50, 256 320. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166276. GABRIEL WEATHERHEAD
  166277. 10769N
  166278. 2/28/96V
  166279. A REVIEW. KUZNETSOV, EVGENII, V.; SHCHERBAKOVA, IRINA V.; BALABAN, ALEXANDRU, T. BENZO[C]PYRILIUM SALTS: SYNTHESES, REACTIONS, AND PHYSICAL PROPERTIES. 1990,50,158 254. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166280. GABRIEL WEATHERHEAD
  166281. 10770N
  166282. 2/28/96VlA REVIEW. QUINOU,HERVE; GUILLOTON,ODETTE. 1,3 THIAZINES 1990, 50, 86 156. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166283. GABRIEL WEATHERHEAD
  166284. 10771N
  166285. 2/28/96
  166286. A REVIEW. PERLMUTTER, HOWARD, D. 1,2 DIAZOCINES, 1,3 DIAZOCINES, TRIAZOCINES AND TETRAZOCINES 1990, 50, 2 83. ADVANCES IN HETEROCYCLIC CHEMISTRYa
  166287. GABRIEL WEATHERHEAD
  166288. 10772N
  166289. 2/28/96V
  166290. A REVIEW. PADWA, ALBERT. GENERATION AND UTILIZATION OF CARBONYL YLIDES VIA THE TANDEM CYCLIZATION CYCLOADDITION METHOD. 1991, 24(1), 22 8. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166291. GABRIEL WEATHERHEAD
  166292. 10773N
  166293. 2/28/96V
  166294. A REVIEW. TROGLER, WILLIAM C. SYNTHESIS, ELECTRONIC STRUCTURE, AND REACTIVITY OF METALLACYCLOTETRAAZAPENTADIENES. 1990, 23(12), 426 31. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166295. GABRIEL WEATHERHEAD
  166296. 10774N
  166297. 2/28/96V
  166298. A REVIEW. BERNARDI, FERNANDO; OLIVUCCI, MASSIMO; ROBB, MICHAEL A. PREDICTING FORBIDDEN AND ALLOWED CYCLOADDITION REACTIONS: POTENTIAL SURFACE TOPOLOGY AND ITS RATIONALIZATION. 1990, 23(12), 405 12. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166299. GABRIEL WEATHERHEAD
  166300. 10775N
  166301. 2/28/96
  166302. A REVIEW. REBEK, JULIUS, JR. MOLECULAR RECOGNITION AND BIOPHYSICAL ORGANIC CHEMISTRY. 1990, 23(12), 399 404. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166303. GABRIEL WEATHERHEAD
  166304. 10776N
  166305. 2/28/96V
  166306. A REVIEW. GUTMAN, DAVID. THE CONTROVERSIAL HEAT OF FORMATION OF THE TERT C4H9 RADICAL AND THE TERTIARY CARBON HYDROGEN BOND ENERGY. 1990, 23(11), 375 80. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166307. GABRIEL WEATHERHEAD
  166308. 10777N
  166309. 2/28/96V
  166310. A REVIEW. GLEITER, ROLF; SCHAEFER, WOLFGANG. INTERACTIONS BETWEEN NONCONJUGATED P SYSTEMS. 1990, 23(11), 369 75. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166311. GABRIEL WEATHERHEAD
  166312. 10778N
  166313. 2/28/96V
  166314. A REVIEW. OKI, MICHINORI. L,9 DISUBSTITUTED TRIPTYCENES: AN EXCELLENT PROBE FOR WEAK MOLECULAR INTERACTIONS. 1990, 23(11), 351 6. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166315. GABRIEL WEATHERHEAD
  166316. 10779N
  166317. 2/28/96VQA REVIEW. WHITE, JAMES D., ED. ORGANIC SYNTHESIS, VOL. 68. WILEY. NEW YORK, 1990.
  166318. GABRIEL WEATHERHEAD
  166319. 10780N
  166320. 2/28/96VjA REVIEW. WELCH, JOHN T.; ESWARAKRISHNAN, SEETHA. FLUORINE IN BIOORGANIC CHEMISTRY. WILEY: NEW YORK, 1991.a
  166321. GABRIEL WEATHERHEAD
  166322. 10781N
  166323. 2/28/96V
  166324. A REVIEW. YICENS, J.; BOHMER, V., EDS. CALIXARENES. A VERSATILE CLASS OF MACROCYCLIC COMPOUNDS. (TOPICS IN INCLUSION SCIENCE). KLUWER ACADEMIC PUBLISHERS: BOSTON, 1990.a
  166325. GABRIEL WEATHERHEAD
  166326. 10782N
  166327. 2/28/96V
  166328. A REVIEW. SILVERSTEIN, R. M.; BASSLER, G. CLAYTON; MORRILL, TERENCE C. SPECTROMETRIC IDENTIFICATION OF ORGANIC COMPOUNDS, 5TH ED. WILEY: NEW YORK, 1991.a
  166329. GABRIEL WEATHERHEAD
  166330. 10783N
  166331. 2/28/96V
  166332. A REVIEW. REHACEK, Z.; SAJDL, P. ERGOT ALKALOIDS: CHEMISTRY, BIOLOGICAL EFFECTS, BIOTECHNOLOGY. (BIOACTIVE MOLECULES, 12). ELSEVIER: AMSTERDAM, 1990.a
  166333. GABRIEL WEATHERHEAD
  166334. 10784N
  166335. 2/28/96
  166336. A REVIEW. RAHMAN, ATTA UR, ED. STUDIES IN NATURAL PRODUCTS CHEMISTRY, VOL. 7: STRUCTURE AND CHEMISTRY, PT. A. ELSEVIER: AMSTERDAM, 1990.a
  166337. GABRIEL WEATHERHEAD
  166338. 10785N
  166339. 2/28/96V
  166340. A REVIEW. OLAH, GEORGE A.; WADE, KENNETH; WILLIAMS, ROBERT E. ELECTRON DEFICIENT BORON AND CARBON CLUSTERS. WILEY: NEW YORK, 1990.a
  166341. GABRIEL WEATHERHEAD
  166342. 10786N
  166343. 2/28/96VpA REVIEW. MULZER, JOHANN, ET AL. ORGANIC SYNTHESIS HIGHLIGHTS. VCH: WEINHEIM, FEDERAL REPUBLIC OF GERMANY, 1990.a
  166344. GABRIEL WEATHERHEAD
  166345. 10787N
  166346. 2/28/96V
  166347. A REVIEW. MEZEY, PAUL G., ED. NEW DEVELOPMENTS IN MOLECULAR CHIRALITY. KLUWER ACADEMIC PUBLISHERS: DORDRECHT, NETHERLANDS, 1991.a
  166348. GABRIEL WEATHERHEAD
  166349. 10788N
  166350. 2/28/96VcA REVIEW. LUND, HENNING; BAIZER, MANUEL M., EDS. ORGANIC MASS SPECTROMETRY. DEKKER: NEW YORK, 1990.a
  166351. GABRIEL WEATHERHEAD
  166352. 10789N
  166353. 2/28/96
  166354. A REVIEW. LUKACS, GABOR; OHNO, MASAJI; EDITORS. RECENT PROGRESS IN THE CHEMICAL SYNTHESIS OF ANTIBIOTICS. SPRINGER BERLIN, FEDERAL REPUBLIC OF GERMANY, 1990.a
  166355. GABRIEL WEATHERHEAD
  166356. 10790N
  166357. 2/28/96V
  166358. A REVIEW. LOEWENTHAL, H. J. E.; ZASS, E. A GUIDE FOR THE PERPLEXED ORGANIC EXPERIMENTALIST. 2ND ED. WILEY: CHICHESTER, U.K., 1990.a
  166359. GABRIEL WEATHERHEAD
  166360. 10791N
  166361. 2/28/96V\A REVIEW. LIOTTA, D. C.; VOLMER, M. ORGANIC SYNTHESES REACTION GUIDE. WILEY: NEW YORK, 1991.a
  166362. GABRIEL WEATHERHEAD
  166363. 10792N
  166364. 2/28/96V
  166365. A REVIEW. JONES, R. ALAN, ED. PYRROLES. PART I: THE SYNTHESIS AND THE PHYSICAL AND  CHEMICAL ASPECTS OF THE PYRROLE RING. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 48, PART 1). WILEY: NEW YORK, 1990.a
  166366. GABRIEL WEATHERHEAD
  166367. 10793N
  166368. 2/28/96V
  166369. A REVIEW. INOUE, Y; GOKEL, G. W., EDS. CATION BINDING BY MACROCYCLES: COMPLEXATION OF CATIONIC SPECIES BY CROWN ETHERS. DEKKER NY, 1990.a
  166370. GABRIEL WEATHERHEAD
  166371. 10794N
  166372. 2/28/96V
  166373. A REVIEW. GRUENANGER, PAOLO; VITA FINZI, PAOLA ISOXAZOLES. PART 1. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 49, PART 1). WILEY: NEW YORK, 1991.a
  166374. GABRIEL WEATHERHEAD
  166375. 10795N
  166376. 2/28/96V
  166377. A REVIEW. GRINBERG, NELU, ED. MODERN THIN LAYER CHROMATOGRAPHY. (CHROMATOGRAPHIC SCIENCE SERIES, VOL. 52). DEKKER: NEW YORK, 1990.a
  166378. GABRIEL WEATHERHEAD
  166379. 10796N
  166380. 2/28/96V
  166381. A REVIEW. GREENHILL, JOHN. V. QUINOLINES. PART 3. JONES,GURNOS, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 32, PART 3). WILEY: CHICHESTER, U.K., 1990.a
  166382. GABRIEL WEATHERHEAD
  166383. 10797N
  166384. 2/28/96VbA REVIEW. FREEMAN , JERMIAH P., ED. ORGANIC SYNTHESES. COLLECTIVE VOLUME 7. WILEY: NEW YORK, 1990.a
  166385. GABRIEL WEATHERHEAD
  166386. 10798N
  166387. 2/28/96V
  166388. A REVIEW. DUERR, H; BOUAS LAURNNT, HENRI, EDS. PHOTOCHROMISM: MOLECULES AND SYSTEMS. (STUDIES IN ORGANIC CHEMISTRY, VOL. 40). ELSEVIER. AMSTERDAM, 1990.a
  166389. GABRIEL WEATHERHEAD
  166390. 10799N
  166391. 2/28/96VcA REVIEW. DESIDENO, DOMINIC, M., ED. MASS SPECTROMETRY OF PEPTIDES CRC PRESS: BOCA RATON, FL, 1990.a
  166392. GABRIEL WEATHERHEAD
  166393. 10800N
  166394. 2/28/96V
  166395. A REVIEW. CRIDDLE, W. J.; ELLIS, G. P. SPECTRAL AND CHEMICAL CHARACTERIZATION OF ORGANIC COMPOUNDS A LABORATORY HANDBOOK. 3RD ED. WILEY. CHICHESTER, U.K., 1990.a
  166396. GABRIEL WEATHERHEAD
  166397. 10801N
  166398. 2/28/96V
  166399. A REVIEW. COLTHUP, NORMAN B.; DALY, LAWRENCE H.; WIBERLEY, STEPHEN E. INTRODUCTION TO INFRADED AND RAMAN SPECTROSCOPY, 3RD. ED. ACADEMIC BOSTON, 1990.a
  166400. GABRIEL WEATHERHEAD
  166401. 10802N
  166402. 2/28/96VqA REVIEW. CHURMS, SHIRLEY C., ED. CRC HANDBOOK OF CHROMATOGRAPHY: CARBOHYDRATES. CRC PRESS: BOCA RATON, FL, 1991.a
  166403. GABRIEL WEATHERHEAD
  166404. 10803N
  166405. 2/28/96VcA REVIEW. CARRUTHERS, W. CYCLOADDITION REACTIONS IN ORGANIC SYNTHYSIS PERGAMON: ELMSFORD, NY, 1990.a
  166406. GABRIEL WEATHERHEAD
  166407. 10804N
  166408. 2/28/96
  166409. A REVIEW. BUGG, CHARLES E.; EALICK, STEVEN E., EDS. CRYSTALLOGRAPHIC AND MODELING METHODS IN MOLECULAR DESIGN. SPRINGER: NEW YORK, 1990.a
  166410. GABRIEL WEATHERHEAD
  166411. 10805N
  166412. 2/28/96VvA REVIEW. BELEN'KII, L. I.; EDITOR. CHEMISTRY OF ORGANOSULFUR COMPOUNDA GENENAL PROBLEMS ELLIS HARWOOD NEW YORK,  1990a
  166413. GABRIEL WEATHERHEAD
  166414. 10806N
  166415. 2/28/96VaA REVIEW. ALBINI, ANGELO; PIETRA, SILVIO. HETEROCYCLIC N OXIDES. CRC PRESS: BOCA RATON, FL, 1990.a
  166416. GABRIEL WEATHERHEAD
  166417. 10807N
  166418. 2/28/96V
  166419. A REVIEW. LU, XIYAN. REACTIONS OF LOW VALENT TRANSITION METAL COMPLEXES WITH COMPOUNDS CONTAINING ALLYLIC C O Z BONDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166420. GABRIEL WEATHERHEAD
  166421. 10808N
  166422. 2/28/96
  166423. A REVIEW. TOMODA, SHUJI; USUKI, YOSHINOSUKE; FUJITA, KEN ICHI; IWAOKA, M. NEW ADDITION OF REACTIONS OF ORGANOSELENIUM REAGENTS ACROSS CARBON CARBON MULTIPLE BONDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166424. GABRIEL WEATHERHEAD
  166425. 10809N
  166426. 2/28/96V
  166427. A REVIEW. KAMIGATA, NOBUMASA; SHIMIZU, TOSHIO. SYNTHESIS, STEREOCHEMISTRY, AND STABILITY OF OPTICALLY ACTIVE SELENOXIDE. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166428. GABRIEL WEATHERHEAD
  166429. 10810N
  166430. 2/28/96V
  166431. A REVIEW. OAE, SHIGERU. LIGAND COUPLING REACTIONS WITHIN HYPERVALENT  SPECIES I. ON SULFUR AND RELATED ATOMS OF GROUP VI ELEMENTS.  BONDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166432. GABRIEL WEATHERHEAD
  166433. 10811N
  166434. 2/28/96
  166435. A REVIEW. MATSUBAYASHI, GEN ETSU. STRUCTURES AND PROPERTIES OF C3S2  (DMIT2 )  AND C3SE2  (DSIS2 ) METAL COMPLEXES. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166436. GABRIEL WEATHERHEAD
  166437. 10812N
  166438. 2/28/96
  166439. %A REVIEW. MIURA, MASAHIRO; NOMURA, MASAKATSU. DESULFONYLATIVE  TRANSFORMATION REACTIONS OF ARYLSULFONYL CHLORIDES CATALYZED BY PALLADIUM COMPLEXES IYZED BY PALLADIUM COMPLESES.  COMPLEXES WITH COMPOUNDS REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.
  166440. GABRIEL WEATHERHEAD
  166441. 10813N
  166442. 2/28/96V
  166443. A REVIEW. LUH, TIEN YAU. METAL CARBONYL PROMOTED CARBON   SULFUR BOND CLEAVAGE REACTIONS SELENIUM REAGENTS ACROSS CARBON CARBON MULTIPLE BONDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166444. GABRIEL WEATHERHEAD
  166445. 10814N
  166446. 2/28/96
  166447. A REVIEW. CAUBERE, PAUL. AGGREGATIVE ACTIVATION: A HELPFUL   CONCEPT OF ORGANIC REACTIVITY AND SYNTHESIS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166448. GABRIEL WEATHERHEAD
  166449. 10815N
  166450. 2/28/96
  166451. >A REVIEW. TAKEUCHI, YOSHIO. CHEMISTRY OF MULTIFUNCTIONAL CARBON  PERVALENT SPECIES I. ON SULFILR AND RELATED ATOM~ OF GROUP  COMPOUNDS I. SYNTHETIC STUDIES AND SOME REACTIONS OF  VT F~LEMENT~.  MULTIFUNCTIONAL CARBON COMPOUNDS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.
  166452. GABRIEL WEATHERHEAD
  166453. 10816N
  166454. 2/28/96V
  166455. A REVIEW. JUARISTI, EUSEBIO. RECENT STUDIES OF THE ANOMERIC EFFECT:    THE INVOLVEMENT OF SULFUR.   THE INVOLVEMENT OF SULFUR. REACTIONS WITHIN HY  REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166456. GABRIEL WEATHERHEAD
  166457. 10817N
  166458. 2/28/96
  166459. A REVIEW. YASUDA, MASAHIDE; SHIMA, KENSUKE. AMINATION OF ELECTRON  RICH SUBSTRATES VIA PHOTOCHEMICAL ELECTRON TRANSFER: MECHANISM AND SYNTHETIC APPLICATION. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166460. GABRIEL WEATHERHEAD
  166461. 10818N
  166462. 2/28/96V
  166463. A REVIEW. EBERHARDT, MANFRED K. HOMOLYTIC AROMATIC HYDROXYLATIONS VIA RADIOLYSIS OF AQUEOUS SOLUTIONS AND VIA METAL ION OXYGEN SYSTEMS. REVIEWS ON HETEROATOM CHEMISTRY. VOLUME 4, SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPAN, 1991.a
  166464. GABRIEL WEATHERHEAD
  166465. 10819N
  166466. 2/28/96V
  166467. A REVIEW. MAXTELL, ARTHUR E. PRE ORGANIZATION AND MOLECULAR RECOGNITION IN THE FORMATION AND REACTIONS OF BINUCLEAR METAL COMPLEXES. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 1, GEORGE W. GOKEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166468. GABRIEL WEATHERHEAD
  166469. 10820N
  166470. 2/28/96
  166471. A REVIEW. MURAKAMI, YUKITO; KIKUCCHI, JUN ICHI; OHNO, TERUHISA. MOLECULAR RECOGNITION BY MACROCYCLES HAVING A THREE DIMENSIONALLY EXTENDED HYDROPHOBIC CAVITY. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 1, GEORGE W. GOKEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.
  166472. GABRIEL WEATHERHEAD
  166473. 10821N
  166474. 2/28/96V
  166475. A REVIEW. SUTHERLAND, IAN O. SYNTHETIC DITOPIC RECEPTORS. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 1, GEORGE W. GOKEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166476. GABRIEL WEATHERHEAD
  166477. 10822N
  166478. 2/28/96V
  166479. A REVIEW. HAMILTON, ANDREW D. HYDROGEN BINDING IN BIOLOGICAL AND ARTIFICIAL MOLECULAR RECOGNITION. ADVANCES IN SUPRAMOLECULAR CHEMISTRY. VOLUME 1, GEORGE W. GOKEL, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166480. GABRIEL WEATHERHEAD
  166481. 10823N
  166482. 2/28/96
  166483. A REVIEW. COREY, JOYCE W. DEHYDROGENATIVE COUPLING REACTIONS OF HYDROSILANES. ADVANCES IN SILICON CHEMISTRY, VOLUME 1, GERALD L. LARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166484. GABRIEL WEATHERHEAD
  166485. 10824N
  166486. 2/28/96V
  166487. A REVIEW. ANDERSON, ROY; ANDERSON, SYDIA A. TRIMETHYLSILYLDIAZOMETHANE. ADVANCES IN SILICON CHEMISTRY, VOLUME 1, GERALD L. LARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166488. GABRIEL WEATHERHEAD
  166489. 10825N
  166490. 2/28/96V
  166491. A REVIEW. SIMCHEN, G. CHEMISTRY OF TRIALKYLSILYL PERFLUORALKANE SULFONATES. ADVANCES IN SILICON CHEMISTRY, VOLUME 1, GERALD L. LARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166492. GABRIEL WEATHERHEAD
  166493. 10826N
  166494. 2/28/96V
  166495. A REVIEW. RASMUSSEN, JERALD K.; HELLMANN, STEVEN; KREPSKI, LARRY R. THE CHEMISTRY OF CYANOTRIMETHYLSILANE. ADVANCES IN SILICON CHEMISTRY, VOLUME 1, GERALD L. LARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166496. GABRIEL WEATHERHEAD
  166497. 10827N
  166498. 2/28/96
  166499. A REVIEW. OLAH, GEORGE A.; PRAKACH, G. K. SURYA; KRISHNAMURTHY, RAMESH. IODOTRIMETHYLSILANE. ADVANCES IN SILICON CHEMISTRY, VOLUME 1, GERALD L. LARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166500. GABRIEL WEATHERHEAD
  166501. 10828N
  166502. 2/28/96
  166503. IA REVIEW. KIBAYASHI, CHIHAIRO. STEREOCONTROLLED NUCLEOPHILIC ADDITIONS TO A B BIS (METHOXYMETHYL) CARBONYL AND IMINO COMPOUNDS: APPLICATION TO ENANTIOSELECTIVE SYNTHESIS OF HETEROCYCLIC NATURAL PRODUCTS. ADVANCES IN HETEROCYCLIC NATURAL PRODUCTS SYNTHESIS. VOLUME 1, WILLIAM H. PEARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.
  166504. GABRIEL WEATHERHEAD
  166505. 10829N
  166506. 2/28/96
  166507. 'A REVIEW. HIGHSMITH, THOMAS K.; MEYERS, ALBERT I. THE ASYMMETRIC SYNTHESIS OF ALKALOIDS: THE A ALKYLATION OF NITROGEN HETEROCYCLES FORMAMIDINE MEDIATED CHIRAL CARBANIONS ADVANCES IN HETEROCYCLIC NATURAL PRODUCTS SYNTHESIS. VOLUME 1, WILLIAM H. PEARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.
  166508. GABRIEL WEATHERHEAD
  166509. 10830N
  166510. 2/28/96V
  166511. A REVIEW. GRIBBLE, GORDON W. SYNTHETIC APPROACHES TO THE ELLIPTICINE ALKALOIDS VIA METALATION AND CYCLOADDITION CHEMISTRY. ADVANCES IN HETEROCYCLIC NATURAL PRODUCTS SYNTHESIS. VOLUME 1, WILLIAM H. PEARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.a
  166512. GABRIEL WEATHERHEAD
  166513. 10831N
  166514. 2/28/96
  166515. A REVIEW. BOECKMAN, ROBERT K.; WALTERS, MICHAEL W. THE SCOPE AND MECHANISM OF THE CYCLOPROPYLIMINIUM ION REARRANGEMENT AND APPLICATIONS TO ALKALOID SYNTHESIS ADVANCES IN HETEROCYCLIC NATURAL PRODUCTS SYNTHESIS. VOLUME 1, WILLIAM H. PEARSON, ED., JAI PRESS, INC.: GREENWICH, CT, 1991.
  166516. GABRIEL WEATHERHEAD
  166517. 10832N
  166518. 2/28/96V
  166519. A REVIEW. MAKOSZA, MIECZYSLAW. VICARIOUS NUCLEOPHILIC SUBSTITUTION OF HYDROGEN IN THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS 1991, (2) 103    111. SYNTHESISa
  166520. GABRIEL WEATHERHEAD
  166521. 10833N
  166522. 2/28/96
  166523. VlA REVIEW. NARASAKA, KOICHI. CHIRAL LEWIS ACIDS IN CATALYTIC ASYMMETRIC REACTIONS. 1991, (1), 1 11. SYNTHESISa
  166524. GABRIEL WEATHERHEAD
  166525. 10834N
  166526. 2/28/96V
  166527. A REVIEW. SHKLOVER, V. E.; NAGAPETYAN, S. S.; STUCHKOV, YU. T. THE STRUCTURE OF NOVEL CONDUCTIVE DITHIOLATE COMPLEXES. 1990, 59(7), 686 706. RUSSIAN CHEMICAL REVIEWSa
  166528. GABRIEL WEATHERHEAD
  166529. 10835N
  166530. 2/28/96V
  166531. A REVIEW. ALDOSHIN,S.M. SPIROPYRANS. STRUCTURAL FEATURES AND PHOTOCHEMICAL PROPERTIES. 1990, 59(7), 663 685. RUSSIAN CHEMICAL REVIEWSa
  166532. GABRIEL WEATHERHEAD
  166533. 10836N
  166534. 2/28/96V
  166535. A REVIEW. SHKOL'NIKOVA, L. M.; PORAI KOSHITS, M. N. STMCTURE OF THE UNCHARGED, ANIONIC, AND CATIONIC FORMS OF AMINOALKYLCARBOXYLIC AND AMINOALKYLPHOSPHONIC COMPLEXONES. 1990, 59(7), 643 662. RUSSIAN CHEMICAL REVIEWSa
  166536. GABRIEL WEATHERHEAD
  166537. 10837N
  166538. 2/28/96
  166539. A REVIEW. ANTIPIN, M. YU. LOW TEMPERATURE X RAY DIFFRACTION USALYSIS: POSSIBILITIES IN THE SOLUTION OF CHEMICAL PROBLEMS. 1990, 59(7), 607 626. RUSSIAN CHEMICAL REVIEWSa
  166540. GABRIEL WEATHERHEAD
  166541. 10838N
  166542. 2/28/96V
  166543. A REVIEW. ZORKII, P. M.; MASUNOV, A. E. X RAY DIFFRACTOMETRIC INVESTIGATIONS OF ELECTRON DENSITY IN ORGANIC CRYSTALS. 1990, 59(7), 592 606. RUSSIAN CHEMICAL REVIEWSa
  166544. GABRIEL WEATHERHEAD
  166545. 10839N
  166546. 2/28/96VyA REVIEW. NIKITINA, T. S. A,B,B TRIFLUOROSTYRENE AND POLYMERS BASED ON IT. 1990, 59(6), 575 589. RUSSIAN CHEMICAL REVIEWSa
  166547. GABRIEL WEATHERHEAD
  166548. 10840N
  166549. 2/28/96
  166550. A REVIEW. KIRSH, YU. E.; SMSOV, S. A.; POPKOV, YU. M.; TIMASHEV, S. F. PERFLUORINATED CARBON CHAIN COPOLYMERS WITH FUNCTIONAL GROUPS AND CATION EXCHANGE MEMBRANES BASED ON THEM: SYNTHESIS, STRUCTURE AND PROPERTIES. 1990, 59(6), 560 574. RUSSIAN CHEMICAL REVIEWS
  166551. GABRIEL WEATHERHEAD
  166552. 10841N
  166553. 2/28/96
  166554. VxA REVIEW. TARASOVA, R. I.; MOSKVA, V. V. CYCLIC MONO  AND DIPHOSPHAZENES. 1990, 59(6), 538 559. RUSSIAN CHEMICAL REVIEWSa
  166555. GABRIEL WEATHERHEAD
  166556. 10842N
  166557. 2/28/96V
  166558. A REVIEW. CHEMYSHEV, E. A.; KOMALENKOVA, N. G. GENERATION AND REACTIONS OF SILYLENES IN THE GAS PHASE. 1990, 59(6), 531 537. RUSSIAN CHEMICAL REVIEWSa
  166559. GABRIEL WEATHERHEAD
  166560. 10843N
  166561. 2/28/96V
  166562. A REVIEW. ALEKSEEVA, N. V.; YAKHONTOV, L. N. REACTIONS OF PYRIDINES, PYRIMIDINES, AND 1,3,5 TRIAZINES WITH NUCLEOPHILIC REAGENTS. L990, 59(6), 514 530. RUSSIAN CHEMICAL REVIEWSa
  166563. GABRIEL WEATHERHEAD
  166564. 10844N
  166565. 2/28/96V
  166566. A REVIEW. BOGUSLAVSKAYA, L. S.; KARTASHOV, A. V.; CHUVATKIN, N. N. SELECTIVE REPLACEMENT OF HYDROGEN AT A SATURATED CARBON ATOM UNDER THE ACTION OF OXIDIZING AGENTS. 1990, 59(6), 501 513. RUSSIAN CHEMICAL REVIEWSa
  166567. GABRIEL WEATHERHEAD
  166568. 10845N
  166569. 2/28/96
  166570. A REVIEW. ZABOLOTSKII, D. A.; MYAGKOVA, G. I.; EVSTIGNEEVA, R. P. INHIBITORS OF THE LIPOXYGENASE CONVERSION OF POLYENOIC ACIDS. 1990, 59(5), 482 500. RUSSIAN CHEMICAL REVIEWSa
  166571. GABRIEL WEATHERHEAD
  166572. 10846N
  166573. 2/28/96V
  166574. A REVIEW. AKHMEDOV, KH. M.; KARIMOV, KH. S.; SHCHERBAKOVA, I.  M.; PORSHNEV, YU. N.; CHERKASHIN, M. I. THE SYNTHESIS AND PROPERTIES OF N (2,3 EPOXYPROPYL)CARBAZOLES AND OLIGOMERS BASED ON THEM. 1990, 59(5), 425 439. RUSSIAN CHEMICAL REVIEWSa
  166575. GABRIEL WEATHERHEAD
  166576. 10847N
  166577. 2/28/96V
  166578. A REVIEW. FOKIN, A. V.; ALLAKHVERDIEV, M. A.; KOLOMIETS, A. F. NEW ADVANCES IN THE CHEMISTRY OF THIIRANS. 1990, 59(5), 40S24. RUSSIAN CHEMICAL REVIEWSa
  166579. GABRIEL WEATHERHEAD
  166580. 10848N
  166581. 2/28/96V
  166582. A REVIEW. PFEFFER, MICHEL. REACTIONS OF CYCLOPALLADATED COMPOUNDS AND ALKYNES: NEW PATHWAYS FOR ORGANIC SYNTHESIS? 1990, 109(12), 567 76. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  166583. GABRIEL WEATHERHEAD
  166584. 10849N
  166585. 2/28/96
  166586. A REVIEW. VERBOOM, W.; REINHOUDT, D. N. TERT AMINO EFFECT IN HETEROCYCLIC SYNTHESIS. RING CLOSURE REACTIONS OF N,N DIALKYL 1,3 DIEN 1 AMINES 1990, 109(5), 311 24. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BASa
  166587. GABRIEL WEATHERHEAD
  166588. 10850N
  166589. 2/28/96V
  166590. A REVIEW. SUZUKI, AKIRA. SYNTHETIC STUDIES VIA THE CROSS COUPLING REACTION OF ORGANOBORON DERIVATIVES WITH ORGANIC HALIDES. 1991, 63(3), 419 22. PURE AND APPLIED CHEMISTRYa
  166591. GABRIEL WEATHERHEAD
  166592. 10851N
  166593. 2/28/96V
  166594. A REVIEW. PELTER, ANDREW; SMITH, KEITH; JONES, KEVIN. SYNTHESIS AND SOME PROPERTIES OF ALKENYL CARBANIONS STABILIZED BY AN A BORON ATOM. 1991, 63(3), 403 6. PURE AND APPLIED CHEMISTRYa
  166595. GABRIEL WEATHERHEAD
  166596. 10852N
  166597. 2/28/96V~A REVIEW. PLESEK, J.; HELMANEK, S.; STIBR, B. EARLY BIRDS THE CHIRAL BORANES. 1991, 63(3), 399 401. PURE AND APPLIED CHEMISTRYa
  166598. GABRIEL WEATHERHEAD
  166599. 10853N
  166600. 2/28/96
  166601. A REVIEW. MELLER, ANTON. THE BORYLATION OF AROMATIC COMPOUNDS BY DEHALOGENATION PRODUCTS OF (DIALKYLAMINO)DIHALOBORANES 1991, 63(3), 395 8. PURE AND APPLIED CHEMISTRYa
  166602. GABRIEL WEATHERHEAD
  166603. 10854N
  166604. 2/28/96V
  166605. A REVIEW. KOESTER, ROLAND; YALPANI, MOHAMED. AN OUTLINE OF THE CHEMISTRY OF BIS(9 BORABICYCLO[3.3.1]NONANE). L991, 63(3), 387 94. PURE AND APPLIED CHEMISTRYa
  166606. GABRIEL WEATHERHEAD
  166607. 10855N
  166608. 2/28/96V{A REVIEW. KAUFMANN, DIETER E.; SCHACHT, WOLFGANG. BENZANNELATED CYCLOBORANES 1991, 63(3), 383 6. PURE AND APPLIED CHEMISTRYa
  166609. GABRIEL WEATHERHEAD
  166610. 10856N
  166611. 2/28/96VzA REVIEW. HOSMANE, NARAYAN S. NEW FRONTIERS IN MAIN GROUP HETEROCARBORANES. 1991, 63(3), 375 8. PURE AND APPLIED CHEMISTRYa
  166612. GABRIEL WEATHERHEAD
  166613. 10857N
  166614. 2/28/96V
  166615. A REVIEW. GRIMES, RUSSELL N. SMALL CARBORANES AS BUILDING BLOCKS IN DESIGNED ORGANOMETALLIC SYNTHESIS. 1991, 63(3), 36~72. PURE AND APPLIED CHEMISTRYa
  166616. GABRIEL WEATHERHEAD
  166617. 10858N
  166618. 2/28/96V
  166619. A REVIEW. EISCH, JOHN J.; SHAFII, BABAK; BOLESLAWSKI, MAREK P. DI P METHANELIKE PHOTOREARRANGEMENTS OF A,B UNSATURATED ORGANOBORANES IN THE SYNTHESIS OF BORIRENES AND BORACARBENOID INTERMEDIATES 1991, 63(3), 36~8. PURE AND APPLIED CHEMISTRYa
  166620. GABRIEL WEATHERHEAD
  166621. 10859N
  166622. 2/28/96VZA REVIEW. BUBNOV, YU. N. ALLYLIC BISBORANES 1991, 63(3), 361 4. PURE AND APPLIED CHEMISTRYa
  166623. GABRIEL WEATHERHEAD
  166624. 10860N
  166625. 2/28/96V
  166626. A REVIEW. BREGADZE, V. I.; KAMPEL, V. TS.; USYATINSKII, A. YA.; GODOVIKOV, N. N. CARBORANYL DERIVATIVES OF MERCURY AND THALLIUM AS SYNTHONS FOR BORON SUBSTITUTED CARBORANES. 1991, 63(3), 357 60. PURE AND APPLIED CHEMISTRYa
  166627. GABRIEL WEATHERHEAD
  166628. 10861N
  166629. 2/28/96V
  166630. A REVIEW. NOETH, HEINRICH; GEISBERGER, GILBERT; LINTI, GERALD; LODERER, DIRK; RATTAY, WILFRIED; SALZBRENNER, ERIK. RECENT ADVANCES IN BORON NITROGEN CHEMISTRY. II. 1991, 63(3), 351 5. PURE AND APPLIED CHEMISTRY
  166631. GABRIEL WEATHERHEAD
  166632. 10862N
  166633. 2/28/96VwA REVIEW. PAETZOLD, P. NEW PERSPECTIVES IN BORON NITROGEN CHEMISTRY. I. 1991, 63(3), 345 50. PURE AND APPLIED CHEMISTRYa
  166634. GABRIEL WEATHERHEAD
  166635. 10863N
  166636. 2/28/96V
  166637. A REVIEW. MATTESON, DONALD 5. RECENT ADVANCES IN ASYMMETRIC SYNTHESIS WITH BORONIC ESTERS. 1991, 63(3), 339 44. PURE AND APPLIED CHEMISTRYa
  166638. GABRIEL WEATHERHEAD
  166639. 10864N
  166640. 2/28/96V
  166641. A REVIEW. GREENWOOD, NORMAN N.; KENNEDY, JOHN D. SOME THOUGHT PROVOKING POLYHEDRAL BORANE CHEMISTRY. 1991, 63(3), 317 26. PURE AND APPLIED CHEMISTRYa
  166642. GABRIEL WEATHERHEAD
  166643. 10865N
  166644. 2/28/96V
  166645. A REVIEW. BROWN, HERBERT C.; RAMACHANDRAN, P. VEERARAGHAVAN. THE BORON APPROACH TO ASYMMETRIC SYNTHESIS. 1991, 63(3), 307 16. PURE AND APPLIED CHEMISTRYa
  166646. GABRIEL WEATHERHEAD
  166647. 10866N
  166648. 2/28/96
  166649. A REVIEW. MAIER, GUNTHER. UNUSUAL MOLECULES UNUSUAL REACTIONS: FROM TETRA TERT BUTYLTETRAHEDRANE TO THE DIMER OF CARBON SULFIDE. 1991, 63(2), 275 82. PURE AND APPLIED CHEMISTRYa
  166650. GABRIEL WEATHERHEAD
  166651. 10867N
  166652. 2/28/96V
  166653. A REVIEW. KOCHI, JAY K. CHARGE TRANSFER EXCITATION OF MOLECULAR COMPLEXES IN ORGANIC AND ORGANOMETALLIC CHEMISTRY. 1991, 63(2), 255 64. PURE AND APPLIED CHEMISTRYa
  166654. GABRIEL WEATHERHEAD
  166655. 10868N
  166656. 2/28/96V
  166657. A REVIEW. NEFEDOV, 0. M. GENERATION, LOW TEMPERATURE STABILIZATION, STRUCTURE, AND REACTIVITY OF INTERMEDIATES WITH LOW COORDINATED CARBON, SILICON, AND GERMANIUM ATOMS. 1991, 63(2), PURE AND APPLIED CHEMISTRYa
  166658. GABRIEL WEATHERHEAD
  166659. 10869N
  166660. 2/28/96V
  166661. A REVIEW. PFANDER, HANSPETER. SYNTHESIS OF OPTICALLY ACTIVE CAROTENOIDS: A REVIEW. 1991, 63(1), 23 33. PURE AND APPLIED CHEMISTRYa
  166662. GABRIEL WEATHERHEAD
  166663. 10870N
  166664. 2/28/96
  166665. A REVIEW. ITO, MASAYOSHI. RECENT PROGRESS IN THE SYNTHESIS OF BUTENOLIDE CAROTENOIDS AND RETINOIDS. 1991, 63(1), 13 22. PURE AND APPLIED CHEMISTRYa
  166666. GABRIEL WEATHERHEAD
  166667. 10871N
  166668. 2/28/96V
  166669. A REVIEW. HOPPE, DIETER; KRAERNER, THOMS; SCHWARK, JAN ROBERT; ZSCHAGE, OLIVER. METALATED 2 ALKENYL CARBARHATES: CHIRAL HOMOENOLATE REAGENTS FOR ASYMMETRIC SYNTHESIS. 1990, 62(10), 1999 2006. PURE AND APPLIED CHEMISTRYa
  166670. GABRIEL WEATHERHEAD
  166671. 10872N
  166672. 2/28/96VrA REVIEW. BROWN, ROGER F. C. ARE FLASH PYROLYTIC REACTIONS USEFUL? 1981, 62(10), 1981 6 PURE AND APPLIED CHEMISTRYa
  166673. GABRIEL WEATHERHEAD
  166674. 10873N
  166675. 2/28/96V
  166676. A REVIEW. BARLUENGA, JOSE; AZNAR, FERNANDO; FUSTERO, SANTOS; TOMAS, MIGUEL. NEW PERSPECTIVES OF CARBO  AND HETERO 1,3 DIENES IN ORGANIC SYNTHESIS. 1990, 62(10),1957 66. PURE AND APPLIED CHEMISTRYa
  166677. GABRIEL WEATHERHEAD
  166678. 10874N
  166679. 2/28/96
  166680. A REVIEW. POSNER, GARY H. NEW SYNTHETIC METHODOLOGY USING ORGANOSULFUR COMPOUNDS. 1990, 62(10),1949 56. PURE AND APPLIED CHEMISTRYa
  166681. GABRIEL WEATHERHEAD
  166682. 10875N
  166683. 2/28/96V
  166684. A REVIEW. OPPOLZER, W. REGIO  AND STEREOCONTROLLED CATALYTIC PALLADIUM  AND NICKEL'ENE TYPE' CYCLIZATIONS. 1991, 62(10), 1941 8. PURE AND APPLIED CHEMISTRYa
  166685. GABRIEL WEATHERHEAD
  166686. 10876N
  166687. 2/28/96V
  166688. A REVIEW. HEATHCOCK, CLAYTON H.; PIETTRE, SEIGE; KATH, JOHN. MECHANISTIC INVESTIGATIONS OF A BIOMIMETIC POLYCYCLIZATION PROCESS THAT LEADS TO THE DAPHNIPHYLLUM ALKALOIDS. 1990, 62(10), 1911 20. PURE AND APPLIED CHEMISTRYa
  166689. GABRIEL WEATHERHEAD
  166690. 10877N
  166691. 2/28/96V
  166692. A REVIEW. HANESSIAN, STEPHEN; FRANCO, JONATHAN; LAROUCHE, BENOIT. THE PSYCHOBIOLOGICAL BASIS OF HEURISTIC SYNTHESIS PLANNING   MAN, MACHINE, AND THE CHIRON APPROACH. 1990, 62(10), 1887 910. PURE AND APPLIED CHEMISTRYa
  166693. GABRIEL WEATHERHEAD
  166694. 10878N
  166695. 2/28/96
  166696. VZA REVIEW. BRESLOW, RONALD. ENZYME MIMICS. 1990, 62(10),1859 66. PURE AND APPLIED CHEMISTRYa
  166697. GABRIEL WEATHERHEAD
  166698. 10879N
  166699. 2/28/96VoA REVIEW. SZANTAY, CSABA. INDOLE ALKALOIDS IN HUMAN MEDICINE. 1990, 62(7), 1299 302. PURE AND APPLIED CHEMISTRYa
  166700. GABRIEL WEATHERHEAD
  166701. 10880N
  166702. 2/28/96V
  166703. A REVIEW. TIDWELL, THOMAS, T. OXIDATION OF ALCOHOLS TO CARBONYL COMPOUNDS VIA ALKOXYSULFONIUM YLIDES: THE MOFFATT, SWERN AND RELATED REACTIONS. 1990, 39, 297 572. ORGANIC REACTIONSa
  166704. GABRIEL WEATHERHEAD
  166705. 10881N
  166706. 2/28/96VWA REVIEW. GRIERSON, DAVID. THE POLONOVSKI REACTION. 1990, 39, 85 295. ORGANIC REACTIONSa
  166707. GABRIEL WEATHERHEAD
  166708. 10882N
  166709. 2/28/96V
  166710. A REVIEW. CHAMBERLIN, A. RICHARD; BLOOM, STEVEN H. LITHIOALKENES FROM ARYLSULPHONYLHYDRAZONES. 1990, 39,1 83. ORGANIC REACTIONSa
  166711. GABRIEL WEATHERHEAD
  166712. 10883N
  166713. 2/28/96
  166714. A REVIEW. MARTIN, NAZARIO; SEOANE, CARLOS  HANACK, MICHAEL. RECENT ADVANCES IN O QUINODIMETHANE CHEMISTRY. 1991, 23(2), 237 72. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166715. GABRIEL WEATHERHEAD
  166716. 10884N
  166717. 2/28/96V
  166718. A REVIEW. PODRAZA, KENNETH F. REGIOSPECIFIC ALKYLATION OF CYCLOHEXENONES. A REVIEW. 1991, 23(2), 217 35. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166719. GABRIEL WEATHERHEAD
  166720. 10885N
  166721. 2/28/96V
  166722. A REVIEW. ST. CLAIR BLACK, DAVID; KUMAR, NARESH. PYRROLOQUINOLINES. 1991, 23(1), 67 92. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166723. GABRIEL WEATHERHEAD
  166724. 10886N
  166725. 2/28/96V
  166726. A REVIEW. BARLUENGA, JOSE; PALACIOS, FRANCISCO. SYNTHESIS AND REACTIVITY OF L5 PHOSPHAZENES. USES AS SYNTHETIC INTERMEDIATES. 1991, 23(1), 1 65. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166727. GABRIEL WEATHERHEAD
  166728. 10887N
  166729. 2/28/96
  166730. A REVIEW. ROSINI, GOFFREDO; BALLINI, ROBERTO; PETRINI, MARINO; MAROTTA, EMANUELA; RIGHI, PAOLO. RECENT PROGRESS IN THE SYNTHESIS AND REACTIVITY OF NITRO KETONES. A REVIEW. 1990, 22(6), 707 46. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONALa
  166731. GABRIEL WEATHERHEAD
  166732. 10888N
  166733. 2/28/96V
  166734. A REVIEW. LEWIS, EDWARD S. RATE EQUILIBRIUM LFER CHARACTERIZATION OF TRANSITION STATES: THE INTERPRETATION OF A. 1990, 3(1), 1 8. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  166735. GABRIEL WEATHERHEAD
  166736. 10889N
  166737. 2/28/96V
  166738. A REVIEW. SHINE, HENRY J. REFLECTIONS ON THE P COMPLEX THEORY OF BENZIDINE REARRANGEMENT. 1989, 2(7), 491 506. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  166739. GABRIEL WEATHERHEAD
  166740. 10890N
  166741. 2/28/96V
  166742. A REVIEW. MARUYAMA, KAZUHIRO; KATAGIRI, TOSHIMASA. MECHANISM OF THE GRIGNARD REACTION. 1989, 2(3), 205 13. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  166743. GABRIEL WEATHERHEAD
  166744. 10891N
  166745. 2/28/96
  166746. A REVIEW. NUDELMAN, NORMA S. THE DIMER MECHANISM IN AROMATIC NUCLEOPHILIC SUBSTITUTION BY AMINES IN APROTIC SOLVENTS. 1989, 2(1), 1 14. JOURNAL OF PHYSICAL ORGANIC CHEMISTRYa
  166747. GABRIEL WEATHERHEAD
  166748. 10892N
  166749. 2/28/96V
  166750. A REVIEW. VASELLA, ANDREA; BAUDIN, GISELE; PANZA, LUIGI. SYNTHESIS OF GLYCOSYL PHOSPHONATES AND RELATED COMPOUNDS. 1991, 2(1), 151 61. HETEROATOM CHEMISTRYa
  166751. GABRIEL WEATHERHEAD
  166752. 10893N
  166753. 2/28/96V
  166754. A REVIEW. MASTRYUKOVA, T. A. SOME AMINOPHOSPHINOCARBOXYLIC ACIDS AND THEIR DERIVATIVES. 1991, 2(1),141 50. HETEROATOM CHEMISTRYa
  166755. GABRIEL WEATHERHEAD
  166756. 10894N
  166757. 2/28/96V
  166758. A REVIEW. JUARISTI, EUSEBIO. SECOND ROW ANOMERIC INTERACTIONS: THE INVOLVEMENT OF PHOSPHORUS. 1990, 1(3), 267 76. HETEROATOM CHEMISTRYa
  166759. GABRIEL WEATHERHEAD
  166760. 10895N
  166761. 2/28/96VvA REVIEW. FUJIWARA, YUZO; IINTOKU, TETSURO; TAKAKI, KEN. LOOK WHAT PALLADIUM CATALYZES. 1990, 20(10), 636 40. CHEMTECHa
  166762. GABRIEL WEATHERHEAD
  166763. 10896N
  166764. 2/28/96V
  166765. A REVIEW. BURGOYNE, WILLIAM F.; DISON, DALE D.; CASEY, JEREMIAH P. ALKYLATING ARYL AMINES SELECTIVELY. 1989, 19(11), 690 7. CHEMTECHa
  166766. GABRIEL WEATHERHEAD
  166767. 10897N
  166768. 2/28/96VNA REVIEW. TANAKA, MASATO. TO ACTIVATE, IRRADIATE! 1989, 19(1), 59 64. CHEMTECHa
  166769. GABRIEL WEATHERHEAD
  166770. 10898N
  166771. 2/28/96V
  166772. A REVIEW. AKIYAMA, ALAN; BEDNARSKI, MARK; KIM, MAHN JOO; SIMON, ETHAN S.; WALDMANN, HERBERT; WHITESIDES, GEORGE M. ENZYMES IN ORGANIC SYNTHESIS. 1988, 18(10), 627 34. CHEMTECHa
  166773. GABRIEL WEATHERHEAD
  166774. 10899N
  166775. 2/28/96VoA REVIEW. FENSELAU, CATHERINE. THE NEW MASS SPECTROMETRY: DESORPTION IONIZATION. 1988, 18(10), 616 19. CHEMTECHa
  166776. GABRIEL WEATHERHEAD
  166777. 10900N
  166778. 2/28/96V
  166779. A REVIEW. PARSHALL, GEORGE W.; NUGENT, WILLIAM A. MAKING PHARMACEUTICALS VIA HOMOGENEOUS CATALYSIS. PART 1. 1988, 18(3), 184 90. CHEMTECHa
  166780. GABRIEL WEATHERHEAD
  166781. 10901N
  166782. 2/28/96
  166783. VwA REVIEW. BURGESS, KEVIN. BUCKMINSTERFULLERENE. GREAT BALLS OF CARBON. 1990, (22), 733. CHEMISTRY AND INDUSTRY (LONDON)a
  166784. GABRIEL WEATHERHEAD
  166785. 10902N
  166786. 2/28/96V
  166787. A REVIEW. PAUL, EDWARD. REACTION SYSTEMS FOR BULK PHARMACEUTICAL PRODUCTION. 1990, (10), 320 5. CHEMISTRY AND INDUSTRY (LONDON)a
  166788. GABRIEL WEATHERHEAD
  166789. 10903N
  166790. 2/28/96V
  166791. A REVIEW. SHELDON, ROGER. INDUSTRIAL SYNTHESIS OF OPTICALLY ACTIVE COMPOUNDS. 1990, (7), 212 19. CHEMISTRY AND INDUSTRY (LONDON)a
  166792. GABRIEL WEATHERHEAD
  166793. 10904N
  166794. 2/28/96V{A REVIEW. SIMPKINS, N. S. NEW STEREOSELECTIVE REACTIONS IN ORGANIC SYNTHESIS. 1990, 19(3), 335 54. CHEMICAL SOCIETY REVIEWSa
  166795. GABRIEL WEATHERHEAD
  166796. 10905N
  166797. 2/28/96V
  166798. A REVIEW. LEE, IKCHOON. CHARACTERIZATION OF TRANSITION STATES FOR REACTIONS IN SOLUTION BY CROSS INTERACTION CONSTANTS. 1990, 19(3), 317 33. CHEMICAL SOCIETY REVIEWSa
  166799. GABRIEL WEATHERHEAD
  166800. 10906N
  166801. 2/28/96
  166802. A REVIEW. BRUCE, MICHAEL I. ORGANOMETALLIC CHEMISTRY OF VINYLIDENE AND RELATED UNSATURATED CARBENES. 1991, 91(2),197 257. CHEMICAL REVIEWSa
  166803. GABRIEL WEATHERHEAD
  166804. 10907N
  166805. 2/28/96V
  166806. A REVIEW. HANSCH, CORWIN; LEO, A.; TAFT, R. W. A SURVEY OF HAMMETT SUBSTITUENT CONSTANTS AND RESONANCE AND FIELD PARAMETERS. 1991, 91(2),165 95. CHEMICAL REVIEWSa
  166807. GABRIEL WEATHERHEAD
  166808. 10908N
  166809. 2/28/96V
  166810. A REVIEW. ALLEN, CHRISTOPHER W. REGIO  AND STEREOCHEMICAL CONTROL IN SUBSTITUTION REACTIONS OF CYCLOPHOSPHAZENES. 1991, 91(2), CHEMICAL REVIEWSa
  166811. GABRIEL WEATHERHEAD
  166812. 10909N
  166813. 2/28/96V
  166814. A REVIEW. CSUK, RENE; GLAENZER, BRIGITTE I. BAKER'S YEAST MEDIATED TRANSFORMATIONS IN ORGANIC CHEMISTRY. 1991, 91(1), 49 97. CHEMICAL REVIEWSa
  166815. GABRIEL WEATHERHEAD
  166816. 10910N
  166817. 2/28/96V
  166818. A REVIEW. MORRISON, JOHN A. CHEMISTRY OF THE POLYHEDRAL BORON HALIDES AND THE DIBORON TETRAHALIDES. 1991, 91(1), 35 48. CHEMICAL REVIEWSa
  166819. GABRIEL WEATHERHEAD
  166820. 10911N
  166821. 2/28/96V~A REVIEW. MUKERJEE, ARYA K.; ASHARE, RAM. ISOTHIOCYANATES IN THE CHEMISTRY OF HETEROCYCLES. 1991, 91(1),1 24. CHEMICAL REVIEWSa
  166822. GABRIEL WEATHERHEAD
  166823. 10912N
  166824. 2/28/96V
  166825. A REVIEW. MINTZ, ERIC A. PREPARATION AND REACTIVITY OF A ZIRCONOCENYL THIOETHERS: NEW CARBON CARBON BOND FORMING REACTIONS VIA A TRANSITION METAL HYDROXYMETHYL OR METALLOXIRANE ANALOG. 1989, 29(4), 443 9. CHEMICA SCRIPTAa
  166826. GABRIEL WEATHERHEAD
  166827. 10913N
  166828. 2/28/96V
  166829. A REVIEW. FRYZUK, MICHAEL D. FUNCTIONALIZATION OF ALKYNES, ENYNES AND ARYNES USING ORGANOZIRCONIUM REAGENTS. 1989, 29(4), 427 37. CHEMICA SCRIPTAa
  166830. GABRIEL WEATHERHEAD
  166831. 10914N
  166832. 2/28/96V
  166833. A REVIEW. BUCHWALD, STEPHEN L.; FISHER, RICHARD A. ZIRCONOCENE COMPLEXES OF UNSATURATED ORGANIC MOLECULES. 1989, 29(4), CHEMICA SCRIPTAa
  166834. GABRIEL WEATHERHEAD
  166835. 10915N
  166836. 2/28/96
  166837. A REVIEW. MORI, KENJI. SYNTHESIS AS AN INDISPENSABLE TOOL FOR THE STUDY OF CHEMICAL COMMUNICATION. 1989, 29(4), 395 400. CHEMICA SCRIPTAa
  166838. GABRIEL WEATHERHEAD
  166839. 10916N
  166840. 2/28/96V
  166841. A REVIEW. VERBOOM, W.; REINHOUDT, D. N. FOUR MEMBERED CYCLIC NITRONES. SYNTHESIS AND REACTIVITY: A REVIEW. 1990, (NOV DEC), 704 13. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  166842. GABRIEL WEATHERHEAD
  166843. 10917N
  166844. 2/28/96V
  166845. A REVIEW. KRIEF, A.; LABOUREUR, J. L.; DUMONT, W.; LABAR, D. TRANSFORMATIONS OF B HYDROXYALKYL SELENIDES TO ALDEHYDES AND KETONES: A REVIEW. 1990, (NOV DEC), 681 96. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  166846. GABRIEL WEATHERHEAD
  166847. 10918N
  166848. 2/28/96V
  166849. A REVIEW. STORK, G. A SURVEY OF THE RADICAL MEDIATED CYCLIZATION OF A HALO ACETALS OF CYCLIC ALLYL ALCOHOLS AS A GENERAL ROUTE TO THE CONTROL OF VICINAL REGIO  AND STEREOCHEMISTRY. 1990, (NOV DEC), 675 80. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  166850. GABRIEL WEATHERHEAD
  166851. 10919N
  166852. 2/28/96V
  166853. A REVIEW. KNAUTH, P.; SAOBAH, R. THERNLOCHEMISTRY OF ORGANIC COMPOUNDS. A REVIEW ON EXPERIMENTAL METHODS AND PRESENT DAY RESEARCH ACTIVITIES. 1990, (MAY JUNE), 329 46. BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCEa
  166854. GABRIEL WEATHERHEAD
  166855. 10920N
  166856. 2/28/96V
  166857. A REVIEW. STODDART, J. FRAAER. THE THIRD ALLOTROPIC FORM OF CARBON. 1991, 30(1), 70 71. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166858. GABRIEL WEATHERHEAD
  166859. 10921N
  166860. 2/28/96V
  166861. A REVIEW. NOYORI, RYOJI; KITAMURA, MAAATO. ENANTIOSELECTIVE ADDITION OF ORGANOMETALLIC REAGENTS TO CARBONYL COINPOUNDS: CHIRALITY TRANSFER, MULTIPLICATION AND AMPLIFICATION. 1991, 30(1), 49 69. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166862. GABRIEL WEATHERHEAD
  166863. 10922N
  166864. 2/28/96V
  166865. A REVIEW. POPE, MICHAEL T.; MUELLER, ACHIM. POLYOXOMETALATE CHEMISTRY. AN OLD THEME WITH NEW DIMENSIONS IN SEVERAL DISCIPLINES. 1991, 30(1), 34 48. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH
  166866. GABRIEL WEATHERHEAD
  166867. 10923N
  166868. 2/28/96V
  166869. A REVIEW. GOTO, TOSHIO; KONDO, TADAO. STRUCTURE AND MOLECULAR STACKING OF ANTHOCYANINS. FLOWER COLOR VARIATION. 1991, 30(1), 17 33. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166870. GABRIEL WEATHERHEAD
  166871. 10924N
  166872. 2/28/96V
  166873. A REVIEW. HOFFMANN, ROALD; LASZLO, PIERRE. REPRESENTATION IN CHEMISTRY. 1991, 30(1), 1 16. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166874. GABRIEL WEATHERHEAD
  166875. 10925N
  166876. 2/28/96V
  166877. A REVIEW. MAYR, HERBERT. CARBON CARBON BOND FORMATION BY ADDITION OF CARBENIUM IONS TO ALKENES: KINETICS AND MECHANISM. 1990, 29(12),1371 84. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166878. GABRIEL WEATHERHEAD
  166879. 10926N
  166880. 2/28/96V
  166881. A REVIEW. SEEBACH, DIETER. ORGANIC SYNTHESIS WHERE NOW? L990, 29(11), 1320 67. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166882. GABRIEL WEATHERHEAD
  166883. 10927N
  166884. 2/28/96
  166885. A REVIEW. LEHN, JEHN MARIE. PERSPECTIVES IN SUPRAMOLECULAR CHEMISTRY. FROM MOLECULAR RECOGNITION TOWARD MOLECULAR INFORMATION PROCESSING AND SELF ORGANIZATION. 1990, 29(11), 1304 19. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166886. GABRIEL WEATHERHEAD
  166887. 10928N
  166888. 2/28/96V
  166889. A REVIEW. HENDRICKSON, JAMES B. ORGANIC SYNTHESIS IN THE AGE OF COMPUTERS. 1990, 29(11),1286 95. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISHa
  166890. GABRIEL WEATHERHEAD
  166891. 10929N
  166892. 2/28/96V
  166893. A REVIEW. HIBBERT, FRANK; EMSLEY, JOHN. HYDROGEN BONDING AND CHEMICAL REACTIVITY. 1990, 26, 255 379. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  166894. GABRIEL WEATHERHEAD
  166895. 10930N
  166896. 2/28/96V
  166897. A REVIEW. IWAMURA, HIIZU. HIGH SPIN ORGANIC MOLECULES AND SPIN ALIGNMENT IN ORGANIC MOLECULAR ASSEMBLIES. 1990, 26, 179 253. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  166898. GABRIEL WEATHERHEAD
  166899. 10931N
  166900. 2/28/96
  166901. 7V~A REVIEW. SUSTMAN, REINER; KORTH, HANS GERT. THE CAPTODATIVE EFFECT. L990, 26, 131 178. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  166902. GABRIEL WEATHERHEAD
  166903. 10932N
  166904. 2/28/96V
  166905. A REVIEW. SAVEANT, JEAN MICHEL. SINGLE ELECTRON TRANSFER AND NUCLEOPHILIC SUBSTITUTION. 1990, 26, 1
  166906. 130. ADVANCES IN PHYSICAL ORGANIC CHEMISTRYa
  166907. GABRIEL WEATHERHEAD
  166908. 10933N
  166909. 2/28/96V
  166910. A REVIEW. FORMOSINHO, SABASTIAO J.; ARNAUT, LUIS G. A UNIFIED VIEW OF KETONE PHOTOCHEMISTRY. 1991,16, 67 117. ADVANCES IN PHOTOCHEMISTRYa
  166911. GABRIEL WEATHERHEAD
  166912. 10934N
  166913. 2/28/96V
  166914. A REVIEW. GUST, DEVENS; MOORE, THOMAS A. MIMICKING PHOTOSYNTHETIC ELECTRON AND ENERGY TRANSFER. 1991,16, L 65. ADVANCES IN PHOTOCHEMISTRYa
  166915. GABRIEL WEATHERHEAD
  166916. 10935N
  166917. 2/28/96V
  166918. A REVIEW. LEGLER, GUNTHER. GLYCOSIDE HYDROLASES: MECHANISTIC INFORMATION FROM STUDIES WITH REVERSIBLE AND IRREVERSIBLE INHIBITORS. 1990, 48, 319 384. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY
  166919. GABRIEL WEATHERHEAD
  166920. 10936N
  166921. 2/28/96V
  166922. A REVIEW. LINDBERG, BENGT. COMPONENTS OF BACTERIAL POLYSACCHARIDES. L99O, 48, 279 318. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  166923. GABRIEL WEATHERHEAD
  166924. 10937N
  166925. 2/28/96V
  166926. A REVIEW. TSUCHIYA, TSUTOMU. CHEMISTRY AND DEVELOPMENTS OF FLUORINATED CARBOHYDRATES. 1990, 48, 91 277. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  166927. GABRIEL WEATHERHEAD
  166928. 10938N
  166929. 2/28/96V
  166930. A REVIEW. SUAMI, TETSUO; OGAWA, SEIICHIRO. CHEMISTRY OF CARBA SUGARS (PSEUDO SUGARS) AND THEIR DERIVATIVES. 1990, 48, 21 90. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRYa
  166931. GABRIEL WEATHERHEAD
  166932. 10939N
  166933. 2/28/96V
  166934. A REVIEW. SMITH, MITCHELL J.; KIM, DOOSEOP; HORENSTEIN, BENJAMIN; NAKANISHI, KOJI; KUSTIN, KENNETH. UNRAVELING THE CHEMISTRY OF TUNICHROME. 1991, 24(4),117 24. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166935. GABRIEL WEATHERHEAD
  166936. 10940N
  166937. 2/28/96
  166938. A REVIEW. GARST, JOHN F. GRIGNARD REAGENT FORMATION AND FREELY DIFFUSING RADICAL INTERMEDIATES. 1991, 24(4), 95 7. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166939. GABRIEL WEATHERHEAD
  166940. 10941N
  166941. 2/28/96V}A REVIEW. DOUGHERTY, DENNIS A. SPIN CONTROL IN ORGANIC MOLECULES. 1991, 24(3), 88 94. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166942. GABRIEL WEATHERHEAD
  166943. 10942N
  166944. 2/28/96V
  166945. A REVIEW. MCCLOSKEY JAMES A. STRUCTURAL CHARACTERIZATION OF NATURAL NUCLEOSIDES BY MASS SPECTROMETRY. 1991, 24(3), 81 8. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166946. GABRIEL WEATHERHEAD
  166947. 10943N
  166948. 2/28/96VyA REVIEW. DJERASSI, CARL; LAM, WAI KWAN. SPONGE PHOSPHOLIPIDS. 1991, 24(3) 69 75. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166949. GABRIEL WEATHERHEAD
  166950. 10944N
  166951. 2/28/96V
  166952. A REVIEW. DOLBIER, WILLIAM R., JR. CYCLOADDITIONS OF FLUOROALLENE AND L,L DIFLUOROALLENE. 1991, 24(3), 63 9. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166953. GABRIEL WEATHERHEAD
  166954. 10945N
  166955. 2/28/96V
  166956. A REVIEW. ASTRUC, DIDIER. TRANSITION METAL RADICALS: CHAMELEON STRUCTURE AND CATALYTIC FUNCTION. 1991, 24(2), 36 42. A REVIEW. ACCOUNTS OF CHEMICAL RESEARCHa
  166957. GABRIEL WEATHERHEAD
  166958. 10946N
  166959. 2/28/96
  166960. 5SHELDON, R. A., KOCHI, J. K. METAL CATALYZED OXIDATIONS OF ORGANIC COMPOUNDS. ACADEMIC PRESS: NEW YORK, 1981.SYNTHESIS, MOLECULAR STRUCTURES, PROPERTIES AND REACTIONS OF HALO(AMINO)COPPER(I) AND CARBONYL(AMINE) COPPER(I) COMPLEXES. CAULTON K. G., DAVIES G., HOLT E. M., PP. 2319 51 (113 REFERENCES). A REVIEW.
  166961. GABRIEL WEATHERHEAD
  166962. 10947N
  166963. 2/28/96VgPINES, H. THE CHEMISTRY OF CATALYTIC HYDROCARBON CONVERSIONS. ACADEMIC PRESS: NEW YORK, 1981. A REVIEW.a
  166964. GABRIEL WEATHERHEAD
  166965. 10948N
  166966. 2/28/96VlNATORI, S.; IKEKAWA, N.; SUZUKI, M. ADVANCES IN NATURAL PRODUCTS CHEMISTRY. WILEY: NEW YORK, 1981. A REVIEW.a
  166967. GABRIEL WEATHERHEAD
  166968. 10949N
  166969. 2/28/96
  166970. LEE, D. G. THE OXIDATION OF ORGANIC COMPOUNDS BY PERMANGANATE ION AND HEXAVALENT CHROMIUM. OPEN COURT PUBLISHING COMPANY: LASALLE, ILLINOIS, 1980. A REVIEW.a
  166971. GABRIEL WEATHERHEAD
  166972. 10950N
  166973. 2/28/96V|JACQUES, J.; COLLET, A.; WILEN, S. H. ENANTIOMERS, RACEMATES, AND RESOLUTIONS. WILEY LNTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  166974. GABRIEL WEATHERHEAD
  166975. 10951N
  166976. 2/28/96VmHERBERT, R. B. BIOSYNTHESIS OF SECONDARY METABOLITES. CHAPMAN & HALL METHUEN, INC.: NEW YORK, 1981. A REVIEW.a
  166977. GABRIEL WEATHERHEAD
  166978. 10952N
  166979. 2/28/96V]GAJEWSKI, J. J. HYDROCARBON THERMAL ISOMERIZATIONS. ACADEMIC PRESS: NEW YORK, 1981. A REVIEW.a
  166980. GABRIEL WEATHERHEAD
  166981. 10953N
  166982. 2/28/96VhCOLVIN, E. W. SILICON IN ORGANIC SYNTHESIS. BUTTERWORTH PUBLISHERS, INC.; MASSACHUSETTS, 1981. A REVIEW.a
  166983. GABRIEL WEATHERHEAD
  166984. 10954N
  166985. 2/28/96
  166986. NVlBAKER, J. T.; MURPHY, V. COMPOUNDS FROM MARINE ORGANISMS, VOL. II. CRC PRESS, INC.: FLORIDA, 1981. A REVIEW.a
  166987. GABRIEL WEATHERHEAD
  166988. 10955N
  166989. 2/28/96VkBAKER, J. T.; MURPHY, V. COMPOUNDS FROM MARINE ORGANISMS, VOL. I. CRC PRESS, INC.: FLORIDA, 1981. A REVIEW.a
  166990. GABRIEL WEATHERHEAD
  166991. 10956N
  166992. 2/28/96V_BAILEY, P. S. OZONATION IN ORGANIC CHEMISTRY, VOL. 2. ACADEMIC PRESS: NEW YORK, 1982. A REVIEW.a
  166993. GABRIEL WEATHERHEAD
  166994. 10957N
  166995. 2/28/96V
  166996. ARNDT D. MANGANESE COMPOUNDS AS OXIDIZING AGENTS IN ORGANIC CHEMISTRY. OPEN COURT PUBLISHING COMPANY: LASALLE, ILLINOIS, 1981. A REVIEW.a
  166997. GABRIEL WEATHERHEAD
  166998. 10958N
  166999. 2/28/96V
  167000. BLASIUS, E.; JANZEN, K. P. ANALYTICAL APPLICATIONS OF CROWN COMPOUNDS AND CRYPTANDS. 1981, 98. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNGS), SPRINGER VERLAG: NEW YORK, 1981 A REVIEW.a
  167001. GABRIEL WEATHERHEAD
  167002. 10959N
  167003. 2/28/96
  167004. VOGTLE, F.; SIEGER, H.; MULLER, W. M. COMPLEXATION OF UNCHARGED MOLECULES AND ANIONS BY CROWN TYPE HOST MOLECULES. 1981, 98. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNGS), SPRINGER VERLAG: NEW YORK, 1981 A REVIEW.a
  167005. GABRIEL WEATHERHEAD
  167006. 10960N
  167007. 2/28/96V
  167008. CRAM, D. J.; TRUEBLOOD, K. N. CONCEPT, STRUCTURE, AND BINDING IN COMPLEXATION. 1981, 98. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNGS), SPRINGER VERLAG: NEW YORK, 1981 A REVIEW.a
  167009. GABRIEL WEATHERHEAD
  167010. 10961N
  167011. 2/28/96V
  167012. WEBER, E.; VOGTLE, F. CROWN TYPE COMPOUNDS
  167013. AN INTRODUCTORY OVERVIEW. 1981, 98. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNGS), SPRINGER VERLAG: NEW YORK, 1981 A REVIEW.a
  167014. GABRIEL WEATHERHEAD
  167015. 10962N
  167016. 2/28/96V
  167017. GASPAR, P. P. SILYLENES, P 335. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167018. GABRIEL WEATHERHEAD
  167019. 10963N
  167020. 2/28/96
  167021. WV}LWOWSKI, W. NITRENES, P 315. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167022. GABRIEL WEATHERHEAD
  167023. 10964N
  167024. 2/28/96V
  167025. KAPLAN L. FREE RADICALS, P 251. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167026. GABRIEL WEATHERHEAD
  167027. 10965N
  167028. 2/28/96V
  167029. BETHELL D., WHITTAKER, D. CARBOCATIONS, P 211. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167030. GABRIEL WEATHERHEAD
  167031. 10966N
  167032. 2/28/96V
  167033. BORDEN, W. T. DIRADICALS, P 175. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167034. GABRIEL WEATHERHEAD
  167035. 10967N
  167036. 2/28/96V
  167037. CASEY, C. W. METAL CARBENE COMPLEXES, P 135. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167038. GABRIEL WEATHERHEAD
  167039. 10968N
  167040. 2/28/96
  167041. MOSS, R. A.; JONES, M., JR. CARBENES, P 59. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167042. GABRIEL WEATHERHEAD
  167043. 10969N
  167044. 2/28/96V
  167045. STALEY, S. W., DUSTMAN, C. K. CARBANIONS, P 15. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167046. GABRIEL WEATHERHEAD
  167047. 10970N
  167048. 2/28/96VzLEVIN, R. H. ARYNES, P 1. REACTIVE INTERMEDIATES, M. JONES, JR., R. A. MOSS, EDS., WILEY: NEW YORK, 1981; VOL. 2 A REVIEW.a
  167049. GABRIEL WEATHERHEAD
  167050. 10971N
  167051. 2/28/96V
  167052. BICK, I. R. C. SINCHAI, W. PHENANTHROINDOLIZIDINES AND PHENANTHROQUINOLIZIDINE ALKALOIDS. 1981,19 THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167053. GABRIEL WEATHERHEAD
  167054. 10972N
  167055. 2/28/96V
  167056. RIPPERGER, H.; SCHREIBER, K. SOLANUM STEROID ALKALOIDS. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167057. GABRIEL WEATHERHEAD
  167058. 10973N
  167059. 2/28/96VyJEFFS, P. W. SCELETIUM ALKALOIDS. 1981,19. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167060. GABRIEL WEATHERHEAD
  167061. 10974N
  167062. 2/28/96V
  167063. HOLLAND, H. L. MICROBIAL AND IN VITRO ENZYMIC TRANSFORMATIONS OF ALKALOIDS. 1981,18. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167064. GABRIEL WEATHERHEAD
  167065. 10975N
  167066. 2/28/96V
  167067. GOLEBIEWSKI, W. M.; WROBEL, J. T. THE LYTHRACEAE ALKALOIDS. 1981, 18. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167068. GABRIEL WEATHERHEAD
  167069. 10976N
  167070. 2/28/96V
  167071. HUGHES, D. W., MACLEAN, D. B. THE 13C NMR SPECTRA OF ISOQUINOLINE ALKALOIDS. 1981,18. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167072. GABRIEL WEATHERHEAD
  167073. 10977N
  167074. 2/28/96
  167075. PELLETIER, S. W. MODY, N. V. THE CHEMISTRY OF C20 DITERPENOID ALKALOIDS. 1981,18. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167076. GABRIEL WEATHERHEAD
  167077. 10978N
  167078. 2/28/96V
  167079. DYKE, 5. F.; QUESSY, S. N. ERYTHRINA AND RELATED ALKALOIDS. 1981, 18. THE ALKALOIDS, R. G. A. RODRIGO, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  167080. GABRIEL WEATHERHEAD
  167081. 10979N
  167082. 2/28/96V
  167083. BARTH, G.; DJERASSI, C. CIRCULAR DICHROISM OF MOLECULES WITH ISOTOPICALLY ENGENDERED CHIRALITY. 1981, 37, 4123. TETRAHEDRON A REVIEW.a
  167084. GABRIEL WEATHERHEAD
  167085. 10980N
  167086. 2/28/96V
  167087. VIOLA, A.; COLLINS, J. J.; FILIPP, N. INTRAMOLECULAR PERICYCLIC REACTIONS OF ACETYLENIC COMPOUNDS. 1981, 37, 3765. TETRAHEDRON A REVIEW.a
  167088. GABRIEL WEATHERHEAD
  167089. 10981N
  167090. 2/28/96V
  167091. BROWN, H. C.; JADHAV, P. K.; MANDAL, A. K. ASYMMETRIC SYNTHESIS VIA CHIRAL ORGANOBORANE REAGENTS. 1981, 37 3547. TETRAHEDRON A REVIEW.a
  167092. GABRIEL WEATHERHEAD
  167093. 10982N
  167094. 2/28/96V~KOST, A. N.; GROMOV, S. P.; SAGITULLIN, R. S. PYRIDINE RING NUCLEOPHILIC RECYCLIZATIONS. 1981, 37, 3423. TETRAHEDRON A REVIEW.a
  167095. GABRIEL WEATHERHEAD
  167096. 10983N
  167097. 2/28/96VtBECKWITH, A. L. J. REGIOSELECTIVITY AND STEREOSELECTIVITY IN RADICAL REACTIONS. 1981, 37 3073. TETRAHEDRON A REVIEW.a
  167098. GABRIEL WEATHERHEAD
  167099. 10984N
  167100. 2/28/96VhBRADY, W. T. SYNTHETIC APPLICATIONS INVOLVING HALOGENATED KETENES. 1981, 37, 2949. TETRAHEDRON A REVIEW.a
  167101. GABRIEL WEATHERHEAD
  167102. 10985N
  167103. 2/28/96ViKROW, G. R. OXYGEN INSERTION REACTIONS OF BRIDGED BICYCLIC KETONES. 1981, 37, 2697. TETRAHEDRON A REVIEW.a
  167104. GABRIEL WEATHERHEAD
  167105. 10986N
  167106. 2/28/96VzSMITH, A. B., III; DIETER, R. K. THE ACID PROMOTED DECOMPOSITION OF A DIAZO KETONES. 1981, 37, 2407. TETRAHEDRON A REVIEW.a
  167107. GABRIEL WEATHERHEAD
  167108. 10987N
  167109. 2/28/96VMFREEMAN, F. REACTIONS OF MALONONITRILE DERIVATIVES. 1981, SYNTHESIS A REVIEW.
  167110. GABRIEL WEATHERHEAD
  167111. 10988N
  167112. 2/28/96V
  167113. NORMANT, J. F.; ALEXAKIS, A. C. METALLATION OF ALKYNES: STEREOSPECIFIC SYNTHESIS OF ALKENYL DERIVATIVES. 1981, 841. SYNTHESIS A REVIEW.a
  167114. GABRIEL WEATHERHEAD
  167115. 10989N
  167116. 2/28/96V
  167117. PETRZILKA, M.; GRAYSON, J. I. PREPARATION AND DIELS ALDER REACTIONS OF HETERO SUBSTITUTED 1,3 DIENES. 1981, 753. SYNTHESIS A REVIEW.a
  167118. GABRIEL WEATHERHEAD
  167119. 10990N
  167120. 2/28/96V
  167121. KONIECZNY M., SOSNOVSKY, G. METHODS FOR THE PREPARATION OF SPIN LABELED PHOSPHORUS COMPOUNDS AND APPLICATIONS OF SOME OF THEM TO PHOSPHORYLATIVE SPIN LABELING. 1981, 682. SYNTHESIS A REVIEW.a
  167122. GABRIEL WEATHERHEAD
  167123. 10991N
  167124. 2/28/96VlOKA, K. SOME APPLICATIONS OF THIONYL CHLORIDE IN SYNTHETIC ORGANIC CHEMISTRY. 1981, 661. SYNTHESIS A REVIEW.a
  167125. GABRIEL WEATHERHEAD
  167126. 10992N
  167127. 2/28/96V`LAI, Y. H. GRIGNARD REAGENTS FROM CHEMICALLY ACTIVATED MAGNESIUM. 1981, 585. SYNTHESIS A REVIEW.a
  167128. GABRIEL WEATHERHEAD
  167129. 10993N
  167130. 2/28/96V
  167131. MESKENS, F. A. J. METHODS FOR THE PREPARATION OF ACETALS FROM ALCOHOLS OR OXIRANES AND CARBONYL COMPOUNDS. 1981, 501. SYNTHESIS A REVIEW.a
  167132. GABRIEL WEATHERHEAD
  167133. 10994N
  167134. 2/28/96V
  167135. BELKIN, YU. V.; POLEZHAEVA, N. A. THE CHEMISTRY OF STABILIZED SULFONIUM YLIDES. 1981, 50, 481. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167136. GABRIEL WEATHERHEAD
  167137. 10995N
  167138. 2/28/96V
  167139. MANOV YUVENSKII, V. I.; NEFEDOV, B. K. SYNTHESIS OF NITROGEN CONTAINING COMPOUNDS BY THE INTERACTION OF NITRO COMPOUNDS WITH CARBON MONOXIDE. 1981, 50, 470. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167140. GABRIEL WEATHERHEAD
  167141. 10996N
  167142. 2/28/96V
  167143. SADEKOV, I. D.; MINKIN, V. I.; SEMENOV, V. V.; SHEVELEV S. A. DOUBLY STABILIZED CHALCOGENONIUM YLIDES. 1981, 50, 432. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167144. GABRIEL WEATHERHEAD
  167145. 10997N
  167146. 2/28/96
  167147. SHEINKER, V. N.; GARNOVSKII, A. D.; OSIPOV, O. A. ADVANCES IN THE STUDY OF S CIS TRANS ISOMERISM STEREOCHEMISTRY OF CARBONYL DERIVATIVES OF FIVE MEMBERED HETEROCYCLES. 1981, 50, 336. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167148. GABRIEL WEATHERHEAD
  167149. 10998N
  167150. 2/28/96V~GRAPOV, A. F.; RAZVODOVSKAYN, L. V., MEL'NIKOV, N. N. DIAZADIPHOSPHETIDINES. 1981, 50, 324. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167151. GABRIEL WEATHERHEAD
  167152. 10999N
  167153. 2/28/96V
  167154. PAVLOVA, L. A.; KOMAROVA, T. V.; DAVIDOVISH, YU. A.ROGOZHIN, S. V. ASPARTAME AND ITS ANALOGUES. 1981, 50, RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167155. GABRIEL WEATHERHEAD
  167156. 11000N
  167157. 2/28/96V
  167158. KHOLMANSKII, A. S.; ZUBKOV, A. V.; DYAMAEV, K. M. THE NATURE OF THE PRIMARY PHOTOCHEMICAL STEP IN SPIROPYRANS. 1981, 50, 305. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167159. GABRIEL WEATHERHEAD
  167160. 11001N
  167161. 2/28/96
  167162. TYULENEVA, V. V.; ROKHLIN, E. M., KNUNYANTS, I. L. FLUORINE CONTAINING HALOGENOMETHYLENEPHOSPHORANES. 1981, 50, 280. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167163. GABRIEL WEATHERHEAD
  167164. 11002N
  167165. 2/28/96V
  167166. MIRONOV, V. F.; GAR, T. K.; FEDOTOV, N. S.; EVERT, G. E. ADAMANTANE STRUCTURES IN THE CHEMISTRY OF SILICON, GERMANIUM, AND TIN. 1981, 50, 262. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167167. GABRIEL WEATHERHEAD
  167168. 11003N
  167169. 2/28/96V
  167170. FESHIN, V. P.; ROMANENKO, L. S.; VORONKOV, M. G. THE A EFFECT IN ORGANIC COMPOUNDS OF GROUP IVB ELEMENTS. 1981, 50, 248. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167171. GABRIEL WEATHERHEAD
  167172. 11004N
  167173. 2/28/96V
  167174. PASHKEVICH, K. I.; SALOUTIN, V. I.; POSTAVSKII, I. YA. FLUORINE CONTAINING BETA DIKETONES. 1981, 50,180. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167175. GABRIEL WEATHERHEAD
  167176. 11005N
  167177. 2/28/96
  167178. YANDOVSKII, V. N.; GIDASPOV, B. V.; TSELINSKII, I. V. THE FORMATION OF THE AZOXY GROUP IN THE OXIDATION OF COMPOUNDS WITH NITROGEN NITROGEN BONDS. 1981, 50, 164. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167179. GABRIEL WEATHERHEAD
  167180. 11006N
  167181. 2/28/96V
  167182. VYUNOV, K. A. GINAK, A. I. THE MECHANISM OF THE ELECTROPHILIC ADDITION OF HALOGENS TO A MULTIPLE BOND. 1981, 50, 151. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167183. GABRIEL WEATHERHEAD
  167184. 11007N
  167185. 2/28/96VlTROFIMOV, B. A. REACTIONS OF ACETYLENE IN SUPERBASIC MEDIA. 1981, 50,138. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167186. GABRIEL WEATHERHEAD
  167187. 11008N
  167188. 2/28/96VwLAPIDUS, A. L.; PING, Y. Y. ORGANIC SYNTHESES BASED ON CARBON DIOXIDE. 1981, 50, 63. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167189. GABRIEL WEATHERHEAD
  167190. 10000
  167191. 11009N
  167192. 2/28/96
  167193. MILESHKEVICH, V. P.; NOVIKOVA, N. F. THE USE OF TAFT RELATIONS FOR THE CORRELATION OF THE PROPERTIES OF ORGANOSILICON COMPOUNDS. THE ROLE OF SUBSTITUENT EFFECTS. 1981 50, 49. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  167194. GABRIEL WEATHERHEAD
  167195. 10001
  167196. 11010N
  167197. 2/28/96V|WYNBERG, H. CHANCE, NECESSITY AND ASYMMETRIC CATALYSIS. 1981, 100, 393. RECUEIL DE TRAVAUX; CHIMIQUES DES PAYS BAS A REVIEW.a
  167198. GABRIEL WEATHERHEAD
  167199. 10002
  167200. 11011N
  167201. 2/28/96V
  167202. SPECKAMP, W. N. RECENT DEVELOPMENTS IN ALKALOID SYNTHESIS. 1981, 100, 345. RECUEIL DE TRAVAUX; CHIMIQUES DES PAYS BAS A REVIEW.a
  167203. GABRIEL WEATHERHEAD
  167204. 10003
  167205. 11012N
  167206. 2/28/96
  167207. VAN KOTEN, G.; VRIEZE, K. INTERACTION OF METAL CENTRES WITH THE 1,4 DIAZA 1,3 BUTADIENE (A DIIMINE) LIGAND. VERSATILE COORDINATION CHEMISTRY AND APPLICATIONS IN ORGANIC SYNTHESIS AND CATALYSIS. 1981,100,129. RECUEIL DE TRAVAUX; CHIMIQUES DES PAYS BAS A REVIEW.
  167208. GABRIEL WEATHERHEAD
  167209. 10004
  167210. 11013N
  167211. 2/28/96
  167212. HANSEN, P. E. CARBON HYDROGEN SPIN SPIN COUPLING CONSTANTS. 1981,14, 175. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY A REVIEW.a
  167213. GABRIEL WEATHERHEAD
  167214. 10005
  167215. 11014N
  167216. 2/28/96VuFRIMER, A. A. THE PHOTOSENSITIZED OXIDATION OF STRAINED OLEFINS. 1981, 21, 194. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167217. GABRIEL WEATHERHEAD
  167218. 10006
  167219. 11015N
  167220. 2/28/96V
  167221. GAJEWSKI, J. J. STEREOCHEMISTRY OF THERMALLY INDUCED HOMOLYTIC FISSION OF C C BOND IN SMALL RINGS. 1981, 21, 169. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167222. GABRIEL WEATHERHEAD
  167223. 10007
  167224. 11016N
  167225. 2/28/96V
  167226. PADWA, A.; BLACKLOCK, T. J.; RIEKER, W. F. SYNTHESIS OF POLYCYCLIC RING SYSTEMS VIA INTRAMOLECULAR [2 + 2] CYCLOADDITION REACTIONS OF CYCLOPROPENE DERIVATIVES. 1981, 21, 157. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167227. GABRIEL WEATHERHEAD
  167228. 10008
  167229. 11017N
  167230. 2/28/96ViPAQUETTE, L. A. THE CHEMISTRY OF SILYLCYCLOPROPANES. 1981, 21, 128. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167231. GABRIEL WEATHERHEAD
  167232. 10009
  167233. 11018N
  167234. 2/28/96V|STANG, P. J. SMALL AND STRAINED RING COMPOUNDS VIA UNSATURATED CARBENES. 1981, 21,119. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167235. GABRIEL WEATHERHEAD
  167236. 10010
  167237. 11019N
  167238. 2/28/96V
  167239. STIRLING, C. J. M. EVALUATION OF STRAIN EFFECTS ON THE REACTIVITY OF SMALL RINGS. 1981, 21,111. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  167240. GABRIEL WEATHERHEAD
  167241. 10011
  167242. 11020N
  167243. 2/28/96V}MUKERJEE, A. K.; KUMAR, P. THE CHEMISTRY OF 4,5 DIHYDRO 6 OXO 1,3 OXAZOLES. 1981,16, 1995. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167244. GABRIEL WEATHERHEAD
  167245. 10012
  167246. 11021N
  167247. 2/28/96VvONO, Y. RING TRANSFORMATIONS OF HETEROCYCLES OVER SYNTHETIC ZEOLITES. 1981,16,1755. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167248. GABRIEL WEATHERHEAD
  167249. 10013
  167250. 11022N
  167251. 2/28/96V|LAI, Y. H. THE CONFORMATIONAL BEHAVIOR IN THIA  AND DITHIAMETACYCLOPHANES. 1981,16, 1739. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167252. GABRIEL WEATHERHEAD
  167253. 10014
  167254. 11023N
  167255. 2/28/96
  167256. ISOBE, K.; KAWAGUCHI, S. ORGANOPALLADIUM(II) COMPLEXES CONTAINING CARBON BONDED PYRIDINE AND PICOLINE AS A LIGAND: PREPARATION, STRUCTURES, AND REACTIONS. 1981,16 1603. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167257. GABRIEL WEATHERHEAD
  167258. 10015
  167259. 11024N
  167260. 2/28/96V
  167261. GELAS, J.; HORTON, D. ACETONATION OF CARBOHYDRATES UNDER KINETIC CONTROL BY USE OF 2 ALKOXYPROPENES. 1981,16,1587. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167262. GABRIEL WEATHERHEAD
  167263. 10016
  167264. 11025N
  167265. 2/28/96V
  167266. MATSUMOTO, K.; UCHIDA, T.; ACHESON, R. M. THE SYNTHESIS AND REACTIONS OF HETEROCYCLES UNDER HIGH PRESSURES. 1981, CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167267. GABRIEL WEATHERHEAD
  167268. 10017
  167269. 11026N
  167270. 2/28/96VwBARONE, R., CHANON, M. SYNTHESIS OF ELLIPTICINE: REVIEW AND COMPUTER SUGGESTIONS. 1981,16, 1357. HETEROCYCLES A REVIEW.a
  167271. GABRIEL WEATHERHEAD
  167272. 10018
  167273. 11027N
  167274. 2/28/96VlSARAF, S. D. PROTON MAGNETIC RESONANCE SPECTRA OF ACRIDIZINIUM ADDUCTS. 1981,16,1243. HETEROCYCLES A REVIEW.
  167275. GABRIEL WEATHERHEAD
  167276. 10019
  167277. 11028N
  167278. 2/28/96V
  167279. GRIMSHAW, J.; DE SILVA, A. P. PHOTOCHEMISTRY AND PHOTOCYCLIZATION OF ARYL HALIDES. 1981,10, 181. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  167280. GABRIEL WEATHERHEAD
  167281. 10020
  167282. 11029N
  167283. 2/28/96VnWILLIAMS, A.; IBRAHIM, I. T. CARBODIIMIDE CHEMISTRY RECENT ADVANCES. 1981, 81, 589. CHEMICAL REVIEWS A REVIEW.a
  167284. GABRIEL WEATHERHEAD
  167285. 10021
  167286. 11030N
  167287. 2/28/96V
  167288. AKELAB, A.; SHERRINGTON, D. C. APPLICATION OF FUNCTIONALIZED POLYMERS IN ORGANIC SYNTHESIS. 1981, 81, 557. CHEMICAL REVIEWS A REVIEW.a
  167289. GABRIEL WEATHERHEAD
  167290. 10022
  167291. 11031N
  167292. 2/28/96V
  167293. CURTIN, D. Y.; PAUL, I. C. CHEMICAL CONSEQUENCES OF THE POLAR AXIS IN ORGANIC SOLID STATE CHEMISTRY. 1981, 81, 525. CHEMICAL REVIEWS A REVIEW.a
  167294. GABRIEL WEATHERHEAD
  167295. 10023
  167296. 11032N
  167297. 2/28/96VoWINNIK, M. A. CYCLIZATION AND THE CONFORMATION OF HYDROCARBON CHAINS. 1981, 81, 491. CHEMICAL REVIEWS A REVIEW.a
  167298. GABRIEL WEATHERHEAD
  167299. 10024
  167300. 11033N
  167301. 2/28/96V}ROFER DEPOORTER, C. K. A COMPREHENSIVE MECHANISM FOR THE FISCHER TROPSCH SYNTHESIS. 1981, 81, 447. CHEMICAL REVIEWS A REVIEW.a
  167302. GABRIEL WEATHERHEAD
  167303. 10025
  167304. 11034N
  167305. 2/28/96VrBHATTACHARYA, A. K., THYAGARAJAN G. THE MICHAELIS ARBUZOV REARRANGEMENT. 1981, 81, 4L5. CHEMICAL REVIEWS A REVIEW.a
  167306. GABRIEL WEATHERHEAD
  167307. 10026
  167308. 11035N
  167309. 2/28/96VUWESTHEIMER, F. H. MONOMERIC METAPHOSPHATES. 1981, 81, 313. CHEMICAL REVIEWS A REVIEW.a
  167310. GABRIEL WEATHERHEAD
  167311. 10027
  167312. 11036N
  167313. 2/28/96VpSCHWARZ, H. PYRAMIDAL CARBOCATIONS. 1981, 20, 991. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167314. GABRIEL WEATHERHEAD
  167315. 10028
  167316. 11037N
  167317. 2/28/96V
  167318. SCHAFER, H. J. ANODIC AND CATHODIC CC BOND FORMATION. 1981, 20, 911. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167319. GABRIEL WEATHERHEAD
  167320. 10029
  167321. 11038N
  167322. 2/28/96
  167323. WAGNER, K.; FINDEISEN, K.; SCHAFER, W.; DIETRICH, W. A,W DIISOCYANATOCARBODIIMIDES,  POLYCARBODIIMIDES, AND THEIR DERIVATIVES. 1981, 20, 819. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167324. GABRIEL WEATHERHEAD
  167325. 10030
  167326. 11039N
  167327. 2/28/96V
  167328. BOSSERT, F.; MEYERS, H.; WEHINGER, E. 4 ARYLDIHYDROPYRIDINES, A NEW CLASS OF HIGHLY ACTIVE CALCIUM ANTAGONISTS. 1981, 20, 762. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167329. GABRIEL WEATHERHEAD
  167330. 10031
  167331. 11040N
  167332. 2/28/96V
  167333. TRUSCHEIT, E., FROMMER, W., JUNGE, B.; MULLER, L.; SCHMIDT, D. D.; WINGENDER, W. CHEMISTRY AND BIOCHEMISTRY OF MICROBIAL A GIUCOSIDASE INHIBITORS. 1981, 20, 744 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167334. GABRIEL WEATHERHEAD
  167335. 10032
  167336. 11041N
  167337. 2/28/96V
  167338. APPEL, R.; KNOLL, F.; RUPPERT, I. PHOSPHA ALKENES AND PHOSPHA ALKYNES; THE (P P)P MULTIPLE BOND. 1981, 20, 731. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167339. GABRIEL WEATHERHEAD
  167340. 10033
  167341. 11042N
  167342. 2/28/96V
  167343. ARLT, D.; JAUTELAT, M.; LANTZSCH, R. SYNTHESIS OF PYRETHROID ACIDS. 1981, 20, 703. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167344. GABRIEL WEATHERHEAD
  167345. 10034
  167346. 11043N
  167347. 2/28/96V
  167348. BUDZIKIEWICZ, H. MASS SPECTROMETRY OF NEGATIVE IONS [NEW ANALYTICAL METHODS (22)]. 1981, 20, 624. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167349. GABRIEL WEATHERHEAD
  167350. 10035
  167351. 11044N
  167352. 2/28/96V
  167353. CHRISTL M. BENZVALENE
  167354. PROPERTIES AND SYNTHETIC POTENTIAL. 1981, 20, 529. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167355. GABRIEL WEATHERHEAD
  167356. 10036
  167357. 11045N
  167358. 2/28/96V
  167359. KATRITZKY, A. R., PATEL, R. C., RIDDELL, F. G. N METHYL INVERSION BARRIERS IN SIX MEMBERED RINGS. 1981, 20, 521. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  167360. GABRIEL WEATHERHEAD
  167361. 10037
  167362. 11046N
  167363. 2/28/96
  167364. HASE, T. A.; KOSKIMIES, J. K. A COMPILATION OF REFERENCES OF FORMYL AND ACYL ANION SYNTHONS. 1981,14, 73. ALDRICHIMICA ACTA A REVIEW.a
  167365. GABRIEL WEATHERHEAD
  167366. 10038
  167367. 11047N
  167368. 2/28/96VeLONG, J. R. THE ROLES OF SILVER SALTS IN ORGANIC PROCESSES. 1981, 14, 63. ALDRICHIMICA ACTA A REVIEW.a
  167369. GABRIEL WEATHERHEAD
  167370. 10039
  167371. 11048N
  167372. 2/28/96VfWIERSUM, U. E. ISOBENZOFURAN AND RELATED O QUINONOID SYSTEMS. 1981,14, 53. ALDRICHIMICA ACTA A REVIEW.a
  167373. GABRIEL WEATHERHEAD
  167374. 10040
  167375. 11049N
  167376. 2/28/96VvTROST, B. M. TRANSITION METAL TEMPLATES FOR SELECTIVITY IN ORGANIC SYNTHESIS. 1981,14, 43. ALDRICHIMICA ACTA A REVIEW.a
  167377. GABRIEL WEATHERHEAD
  167378. 10041
  167379. 11050N
  167380. 2/28/96VvBONNETT, R.; NORTH, S. A. THE CHEMISTRY OF THE ISOINDOLES. 1981, 29, 342. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167381. GABRIEL WEATHERHEAD
  167382. 10042
  167383. 11051N
  167384. 2/28/96
  167385. VqGASCO, A.; BOULTON, A. J. FUROXANS AND BENZOFUROXANS. 1981, 29, 252. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167386. GABRIEL WEATHERHEAD
  167387. 10043
  167388. 11052N
  167389. 2/28/96V
  167390. SCROWSTON, R. M. RECENT ADVANCES IN THE CHEMISTRY OF BENZO[B]THIOPHENES. 1981, 29,1972.ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167391. GABRIEL WEATHERHEAD
  167392. 10044
  167393. 11053N
  167394. 2/28/96V
  167395. RUCCIA, M.; VIVONA, N., SPINELLI, D. MONONUCLEAR HETEROCYCLIC REARRANGEMENTS. 1981, 29,142. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167396. GABRIEL WEATHERHEAD
  167397. 10045
  167398. 11054N
  167399. 2/28/96V
  167400. TAMURA, Y.; IKEDA, M. ADVANCES IN THE CHEMISTRY OF HETEROAROMATIC N IMINES AND N AMINOAZONIUM SALTS. 1981, 29, 73. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167401. GABRIEL WEATHERHEAD
  167402. 10046
  167403. 11055N
  167404. 2/28/96V
  167405. SMALLEY R. K. THE CHEMISTRY OF INDOXAZENES AND ANTHRANILS: 1966 1979. 1981, 29, 2. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167406. GABRIEL WEATHERHEAD
  167407. 10047
  167408. 11056N
  167409. 2/28/96
  167410. WENTRUP, C. CARBENES AND NITRENES IN HETEROCYCLIC CHEMISTRY: INTRAMOLECULAR REACTIONS. 1981, 28, 232. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167411. GABRIEL WEATHERHEAD
  167412. 10048
  167413. 11057N
  167414. 2/28/96V
  167415. BRYCE, M. R.; VERNON, J. M. REACTIONS OF BENZYNE WITH HETEROCYCLIC COMPOUNDS. 1981, 28,183. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167416. GABRIEL WEATHERHEAD
  167417. 10049
  167418. 11058N
  167419. 2/28/96V
  167420. KAPPE, T.; STADLBAUER, W. ISATOIC ANHYDRIDES AND THEIR USES IN HETEROCYCLIC SYNTHESIS. 1981, 28,127. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167421. GABRIEL WEATHERHEAD
  167422. 10050
  167423. 11059N
  167424. 2/28/96V
  167425. LOMBARDINO, J. G.; KUHLA, D. E. 1,2  AND 2,1 BENZOTHIAZINES AND RELATED COMPOUNDS. 1981, 28, 73. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167426. GABRIEL WEATHERHEAD
  167427. 10051
  167428. 11060N
  167429. 2/28/96V}CHAMBERS, R. D.; SARGENT, C. R. POLYFLUOROHETEROAROMATIC COMPOUNDS. 1981, 28, 1. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  167430. GABRIEL WEATHERHEAD
  167431. 10052
  167432. 11061N
  167433. 2/28/96VhDANISHEFSKY, S. SILOXY DIENES IN TOTAL SYNTHESIS. 1981, 14, 400. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167434. GABRIEL WEATHERHEAD
  167435. 10053
  167436. 11062N
  167437. 2/28/96V
  167438. SNIECKUS, V.; STREITH, J. 1,2 DIAZEPINES: A NEW VISTA IN HETEROCYCLIC CHEMISTRY. 1981,14, 348. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167439. GABRIEL WEATHERHEAD
  167440. 10054
  167441. 11063N
  167442. 2/28/96V
  167443. CAPON, B.; GHOSH, A. K.; GRIEVE, D. MCL. A. DIRECT OBSERVATION OF SIMPLE TETRAHEDRAL INTERMEDIATES. 1981,14, 306.ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167444. GABRIEL WEATHERHEAD
  167445. 10055
  167446. 11064N
  167447. 2/28/96V
  167448. ISHII, H. NUCLEOPHILIC DISPLACEMENT OF THE METHOXY GROUP IN ABNORMAL FISCHER INDOLIZATION OF 2 METHOXYPHENYLHYDRAZONES. 1981,14, 275. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167449. GABRIEL WEATHERHEAD
  167450. 10056
  167451. 11065N
  167452. 2/28/96VfORCHIN,M. HCO(CO)4,THE QUINTESSENTIAL CATALYST. 1981, 14, 259. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167453. GABRIEL WEATHERHEAD
  167454. 10057
  167455. 11066
  167456. 2/28/96V
  167457. MELLONI, G., MODENA, G., TONELLATO, U. RELATIVE REACTIVITIES OF CARBON CARBON DOUBLE AND TRIPLE BONDS TOWARD ELECTROPHILES. 1981,14, 227. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167458. GABRIEL WEATHERHEAD
  167459. 10058
  167460. 11067N
  167461. 2/28/96VwHARVEY, R. G. ACTIVATED METABOLITES OF CARCINOGENIC HYDROCARBONS. 1981,14, 218. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167462. GABRIEL WEATHERHEAD
  167463. 10059
  167464. 11068N
  167465. 2/28/96V
  167466. MINKIN, V. I.; OLEKHNOVICH, L. P.; ZHDANOV, Y. A. MOLECULAR DESIGN OF TAUTOMERIC COMPOUNDS. 1981,14, 210. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167467. GABRIEL WEATHERHEAD
  167468. 10060
  167469. 11069N
  167470. 2/28/96V~DOLBIER, W. R., JR. THERMAL REARRANGEMENTS OF GEM DIFLUOROCYCLOPROPANES. 1981,14, 195. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  167471. GABRIEL WEATHERHEAD
  167472. 10061
  167473. 11070N
  167474. 2/28/96V
  167475. THE ACYLOIN CONDENSATION: JORDAN J. BLOOMFIELD, DENNIS C. OWSLEY, AND JANICE M. NELKE ORGANIC REACTIONS VOLUME 23 (1976) A REVIEW.a
  167476. GABRIEL WEATHERHEAD
  167477. 10062
  167478. 11071N
  167479. 2/28/96V
  167480. REDUCTION AND RELATED REACTIONS OF ALPHA, BETA UNSATURATED COMPOUNDS WITH METALS IN LIQUID AMMONIA:  DRURY CAINE, ORGANIC REACTIONS VOLUME 23 (1976) A REVIEW.a
  167481. GABRIEL WEATHERHEAD
  167482. 10063
  167483. 11072N
  167484. 2/28/96VYTHE REFORMATSKY REACTION: MICHAEL W. RATHKE, ORGANIC REACTIONS VOLUME 22 (1975) A REVIEW.a
  167485. GABRIEL WEATHERHEAD
  167486. 10064
  167487. 11073N
  167488. 2/28/96VvCLEMMENSEN REDUCTION OF KETONES IN ANHYDROUS ORGANIC SOLVENTS: E. VEDEJS, ORGANIC REACTIONS VOLUME 22 (1975) A REVIEW.a
  167489. GABRIEL WEATHERHEAD
  167490. 10065
  167491. 11074N
  167492. 2/28/96VqSUBSTITUTION REACTIONS USING ORGANOCOPPER REAGENTS:  GARY H. POSNER, ORGANIC REACTIONS VOLUME 22 (1975) A REVIEW.a
  167493. GABRIEL WEATHERHEAD
  167494. 10066
  167495. 11075N
  167496. 2/28/96V|THE CLAISEN AND COPE REARRANGEMENTS:  SARA JANE RHOADS AND N . REBECCA RAULINS, ORGANIC REACTIONS VOLUME 22 (1975) A REVIEW.a
  167497. GABRIEL WEATHERHEAD
  167498. 10067
  167499. 11076N
  167500. 2/28/96
  167501. VzMODERN METHODS TO PREPARE MONOFLUOROALIPHATIC COMPOUNDS: WILLIAM A. SHEPPARD, ORGANIC REACTIONS VOLUME 21 (1974) A REVIEW.a
  167502. GABRIEL WEATHERHEAD
  167503. 10068
  167504. 11077N
  167505. 2/28/96V
  167506. FLUORINATION WITH SULFUR TETRAFLUORIDE:  G. A. BOSWELL, JR., W. C RIPKA, R M. SCRIBNER, AND C. W. TULLOCK ORGANIC REACTIONS VOLUME 21 (1974) A REVIEW.a
  167507. GABRIEL WEATHERHEAD
  167508. 10069
  167509. 11078N
  167510. 2/28/96V_THE ZININ REDUCTION OF NITROARENES:  H. K. PORTER, ORGANIC REACTIONS VOLUME 20 (1973) A REVIEW.a
  167511. GABRIEL WEATHERHEAD
  167512. 10070
  167513. 11079N
  167514. 2/28/96V
  167515. THE SYNTHESIS OF 5 HYDROXYINDOLES BY THE NENITZESCU REACTION: GEORGE R. ALLEN, JR., ORGANIC REACTIONS VOLUME 20 (1973) A REVIEW.a
  167516. GABRIEL WEATHERHEAD
  167517. 10071
  167518. 11080N
  167519. 2/28/96VpSENSITIZED PHOTOOXYGENATION OF OLEFINS:  R. W. DENNY AND A. NICKON, ORGANIC REACTIONS VOLUME 20 (1973) A REVIEW.a
  167520. GABRIEL WEATHERHEAD
  167521. 10072
  167522. 11081N
  167523. 2/28/96
  167524. CYCLOPROPANES FROM UNSATURATED COMPOUNDS, METHYLENE IODIDE, AND ZINC COPPER COUPLE:  H. E. SIMMONS, T. L. CAIRNS, SUSAN A. VLADUCHICK, AND CONNIE M. HOINESS ORGANIC REACTIONS VOLUME 20 (1973) A REVIEW.a
  167525. GABRIEL WEATHERHEAD
  167526. 10073
  167527. 11082N
  167528. 2/28/96V
  167529. OXIDATIVE DECARBOXYLUTION OF ACIDS BY LEAD TETRAACETATE:  ROGER A. SHELDON AND JAY K. KOCHI, ORGANIC REACTIONS VOLUME 19 (1972) A REVIEW.a
  167530. GABRIEL WEATHERHEAD
  167531. 10074
  167532. 11083N
  167533. 2/28/96V
  167534. FORMATION OF CARBON CARBON BONDS VIA PI ALLYLNICKEL COMPOUNDS: MARTIN F. SEMMELHACK, ORGANIC REACTIONS VOLUME 19 (1972) A REVIEW.a
  167535. GABRIEL WEATHERHEAD
  167536. 10075
  167537. 11084N
  167538. 2/28/96VtCONJUGATE ADDITION REACTIONS OF ORGANOCOPPER REAGENTS:  GARY H. POSNER, ORGANIC REACTIONS VOLUME 19 (1972) A REVIEW.a
  167539. GABRIEL WEATHERHEAD
  167540. 10076
  167541. 11085N
  167542. 2/28/96V}THE BASE PROMOTED REARRANGEMENTS OF QUATERNARY AMMONIUM SALTS:  STANLEY H. PINE, ORGANIC REACTIONS VOLUME 18 (1970) A REVIEW.a
  167543. GABRIEL WEATHERHEAD
  167544. 10077
  167545. 11086N
  167546. 2/28/96V
  167547. THE REACTIONS OF DIAZOACETIC ESTERS VITH ALKENES, ALKYNES, HETEROCYCLIC, AND AROMATIC COMPOUNDS:  VINOD DAVID AND E. W. WARNHOFF, ORGANIC REACTIONS VOLUME 18 (1970) A REVIEW.a
  167548. GABRIEL WEATHERHEAD
  167549. 10078
  167550. 11087N
  167551. 2/28/96V
  167552. THE SMILES AND RELATED REARRANGEMENTS OF AROMATIC SYSTEMS:  W. E. TRUCE, EUNICE M. KREIDER, AND WILLIAM W. BRAND, ORGANIC REACTIONS VOLUME 18 (1970) A REVIEW.a
  167553. GABRIEL WEATHERHEAD
  167554. 10079
  167555. 11088N
  167556. 2/28/96V
  167557. PREPARATION OF KETONES FROM THE REACTION OF ORGANOLITHIUM REAGENTS VITH CARBOXYLIC ACIDS:  MARGARET J. JORGENSON, ORGANIC REACTIONS VOLUME 18 (1970) A REVIEW.a
  167558. GABRIEL WEATHERHEAD
  167559. 10080
  167560. 11089N
  167561. 2/28/96VcTHE RITTER REACTION:  L. I. KRIMEN AND DONALD J. COTA, ORGANIC REACTIONS VOLUME 17 (1969) A REVIEW.a
  167562. GABRIEL WEATHERHEAD
  167563. 10081
  167564. 11090N
  167565. 2/28/96
  167566. THE GAMMA ALKYLATION AND GAMMA ARYLATION OF DIANIONS OF BETA DICARBONYL COMPOUNDS:  THOMAS M. HARRIS AND CONSTANCE M. HARNS, ORGANIC REACTIONS VOLUME 17 (1969) A REVIEW.a
  167567. GABRIEL WEATHERHEAD
  167568. 10082
  167569. 11091N
  167570. 2/28/96V
  167571. THE SYNTHESIS OF SUBSTITUTED FERROCENES AND OTHER PI CYCLOPENTADIENYL TRANSITION METAL COMPOUNDS:  DONALD E. BUBLITZ AND KENNETH L. RINEHART, JR., ORGANIC REACTIONS VOLUME 17 (1969) A REVIEW.a
  167572. GABRIEL WEATHERHEAD
  167573. 10083
  167574. 11092N
  167575. 2/28/96VoTHE ALDOL CONDENSATION:  ARNOLD T NIELSEN AND WILLIAM J. HOULIHAN, ORGANIC REACTIONS VOLUME 16 (1968) A REVIEW.a
  167576. GABRIEL WEATHERHEAD
  167577. 10084
  167578. 11093N
  167579. 2/28/96VUTHE KNOEVENAGEL CONDENSATION:  G. JONES, ORGANIC REACTIONS VOLUME 15 (1967) A REVIEW.a
  167580. GABRIEL WEATHERHEAD
  167581. 10085
  167582. 11094N
  167583. 2/28/96VtTHE DIECKMANN CONDENSATION:  JOHN P. SCHAEFER AND JORDAN J. BLOOMFIELD, ORGANIC REACTIONS VOLUME 15 (1967) A REVIEW.a
  167584. GABRIEL WEATHERHEAD
  167585. 10086
  167586. 11095N
  167587. 2/28/96
  167588. VUTHE WITTIG REACTION:  ADALBERT MAERCKER, ORGANIC REACTIONS VOLUME 14 (1965) A REVIEW.a
  167589. GABRIEL WEATHERHEAD
  167590. 10087
  167591. 11096N
  167592. 2/28/96VvALPHA AMIDOALKYLATIONS AT CARBON:  HAROLD E. ZAUGG AND WILLIAM B. MARTIN, ORGANIC REACTIONS VOLUME 14 (1965) A REVIEW.a
  167593. GABRIEL WEATHERHEAD
  167594. 10088
  167595. 11097N
  167596. 2/28/96ViTHE CHAPMAN REARRANGEMENT:  J. W. SCHULENBERG AND S. ARCHER, ORGANIC REACTIONS VOLUME 14 (1965) A REVIEW.a
  167597. GABRIEL WEATHERHEAD
  167598. 10089
  167599. 11098N
  167600. 2/28/96V
  167601. FORMATION OF CARBON HETEROATOM BONDS BY FREE RADICAL CHAIN ADDITIONS TO CARBON CARBON MULTIPLE BONDS:  F. W STACEY AND J. F. HARRIS, JR., ORGANIC REACTIONS VOLUME 13 (1963) A REVIEW.a
  167602. GABRIEL WEATHERHEAD
  167603. 10090
  167604. 11099N
  167605. 2/28/96V
  167606. FREE RADICAL ADDITIONS TO OLEFINS TO FORM CARBON CARBON BONDS: CHEVES WALLING AND EARL S. HUYSER, ORGANIC REACTIONS VOLUME 13 (1963) A REVIEW.a
  167607. GABRIEL WEATHERHEAD
  167608. 10091
  167609. 11100N
  167610. 2/28/96
  167611. V}HALOCYCLOPROPANES FROM HALOCARBENES:  WILLIAM E. PARHAM AND EDWARD E. SCHWEIZER, ORGANIC REACTIONS VOLUME 13 (1963) A REVIEW.a
  167612. GABRIEL WEATHERHEAD
  167613. 10092
  167614. 11101N
  167615. 2/28/96V
  167616. HYDRATION OF OLEFINS, DIENES, AND ACETYLENES VIA HYDROBORATION GEORGE ZWEIFEL AND HERBERT C BROWN, ORGANIC REACTIONS VOLUME 13 (1963) A REVIEW.a
  167617. GABRIEL WEATHERHEAD
  167618. 10093
  167619. 11102N
  167620. 2/28/96V
  167621. CYCLOBUTANE DERIVATIVES FROM THERMAL CYCLOADDITION REACTIONS JOHN D ROBERTS AND CLAY M SHARTS, ORGANIC REACTIONS VOLUME 12 (1962) A REVIEW.a
  167622. GABRIEL WEATHERHEAD
  167623. 10094
  167624. 11103N
  167625. 2/28/96VkTHE BECKMANN REARRANGEMENT  L GUY DONARUMA AND WALTER Z HELDT, ORGANIC REACTIONS VOLUME 11 (1960) A REVIEW.a
  167626. GABRIEL WEATHERHEAD
  167627. 10095
  167628. 11104N
  167629. 2/28/96V]THE JAPP KLINGEMANN REACTION  ROBERT R PHILLIPS, ORGANIC REACTIONS VOLUME 10 (1959) A REVIEW.a
  167630. GABRIEL WEATHERHEAD
  167631. 10096
  167632. 11105N
  167633. 2/28/96
  167634. V}THE COUPLING OF DIAZONIUM SALTS WITH ALIPHATIC CARBON ATOMS STANLEY M PARMERTER, ORGANIC REACTIONS VOLUME 10 (1959) A REVIEW.a
  167635. GABRIEL WEATHERHEAD
  167636. 10097
  167637. 11106N
  167638. 2/28/96V
  167639. THE CLEAVAGE OF NON ENOLIZABLE KETONES WITH SODIUM AMIDE  K E HAMLIN AND ARTHUR W WESTON, ORGANIC REACTIONS VOLUME 9 (1957) A REVIEW.a
  167640. GABRIEL WEATHERHEAD
  167641. 10098
  167642. 11107N
  167643. 2/28/96V
  167644. THE SYNTHESIS OF KETONES FROM ACID HDIDES ND ORGANOMETALLIC COMPOUNDS OF MANESIUM, ZINC, AND CADMIUM  DAVID A SHIRLEY, ORGANIC REACTIONS VOLUME 8 (1954) A REVIEW.a
  167645. GABRIEL WEATHERHEAD
  167646. 10099
  167647. 11108N
  167648. 2/28/96VhCATALYLIC HYDROGENATION OF ESTERS TO ALCOHOLS  HOMER ADKINS, ORGANIC REACTIONS VOLUME 8 (1954) A REVIEW.a
  167649. GABRIEL WEATHERHEAD
  167650. 10100
  167651. 11109N
  167652. 2/28/96V
  167653. EPOXIDATION AND HYDROXYLATION OF ETHYLENIC COMPOUNDS WITH ORGANIC PERACIDS  DANIEL SWERN, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167654. GABRIEL WEATHERHEAD
  167655. 10101
  167656. 11110N
  167657. 2/28/96
  167658. VeTHE NITROSATION OF ALIPHATIC CARBON ATOMS  OSCAR TOUSTER, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167659. GABRIEL WEATHERHEAD
  167660. 10102
  167661. 11111N
  167662. 2/28/96V
  167663. HYDROGENOLYSIS OF BENZYL GROUPS ATTACHED TO OXYGEN, NITROGEN, OR SULFUR WALTER H HARTUNG AND ROBERT SIMONOFF, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167664. GABRIEL WEATHERHEAD
  167665. 10103
  167666. 11112N
  167667. 2/28/96VeTHE VON BRAUN CYANOGEN BROMIDE REACTION  HOWARD A HAPMAN, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167668. GABRIEL WEATHERHEAD
  167669. 10104
  167670. 11113N
  167671. 2/28/96V
  167672. CARBON CARBON ALKYLATIONS WITH AMINES AND AMMONIUM SALTS JAMES H BREWSTER AND ERNEST L ELIEL, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167673. GABRIEL WEATHERHEAD
  167674. 10105
  167675. 11114N
  167676. 2/28/96VpTHE SKRAUP SYNTHESIS OF QUINOLINES  R H F MANSKE AND MARSHALL KULKA, ORGANIC REACTIONS VOLUME 7 (1953) A REVIEW.a
  167677. GABRIEL WEATHERHEAD
  167678. 10106
  167679. 11115N
  167680. 2/28/96
  167681. VdREDUCTIONS BY LITHIUM ALUMINUM HYDRIDE  WELDON G. BROWN, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167682. GABRIEL WEATHERHEAD
  167683. 10107
  167684. 11116N
  167685. 2/28/96V
  167686. THE PREPURATION OF THIOPHENES AND TETRAHYDROTHIOPHENES:  DONALD E. WOLF AND KARL FOLKERS, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167687. GABRIEL WEATHERHEAD
  167688. 10108
  167689. 11117N
  167690. 2/28/96V}THE PREPARATION OF THIAZOLES:  RICHARD H. WILEY, D. C. ENGLAND AND LYELL C. BEHR, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167691. GABRIEL WEATHERHEAD
  167692. 10109
  167693. 11118N
  167694. 2/28/96V
  167695. THE HALOGEN METAL INTERCONVERSION REACTION WITH ORGANOLITHIUM COMPOUNDS: REUBEN G. JONES AND HENRY GILMAN, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167696. GABRIEL WEATHERHEAD
  167697. 10110
  167698. 11119N
  167699. 2/28/96VuTHE SYNTHESIS OF PHOSPHONIC AND PHOSPHINIC ACIDS:  GENNADY M. KOSOLAPOFF, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167700. GABRIEL WEATHERHEAD
  167701. 10111
  167702. 11120N
  167703. 2/28/96
  167704. VTTHE OPPENANER OXIDATION:  CARL DJERASSI, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167705. GABRIEL WEATHERHEAD
  167706. 10112
  167707. 11121N
  167708. 2/28/96V
  167709. THE SYNTHESIS OF ISOQUINOLINES BY THE POMERANZ FRITSCH REACTION: WALTER J. GENSLER, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167710. GABRIEL WEATHERHEAD
  167711. 10113
  167712. 11122N
  167713. 2/28/96V
  167714. THE PICTET SPENGLER SYNTHESIS OF TETRAHYDROISOQUINOLINES AND RELATED COMPOUNDS:  WILSON M. WHALEY AND TUTICORIN R. GOVINDACHAN, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167715. GABRIEL WEATHERHEAD
  167716. 10114
  167717. 11123N
  167718. 2/28/96V
  167719. THE PREPARATION OF 3,4 DIHYDROISOQUINOLINES AND RELATED COMPOUNDS BY THE BISCHLER NAPIERAISKI REACTION:  WILSON M. WHALEY AND TUTICORIN R. GOVINDACHARI, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167720. GABRIEL WEATHERHEAD
  167721. 10115
  167722. 11124N
  167723. 2/28/96VkTHE STOBBE CONDENSATION:  WILLIAM S. JOHNSON AND GUIDO H. DAUB, ORGANIC REACTIONS VOLUME 6 (1951) A REVIEW.a
  167724. GABRIEL WEATHERHEAD
  167725. 10116
  167726. 11125
  167727. 2/28/96V~THE DARZENS GLYCIDIC ESTER CONDENSATION: MELVIN S. NEWMAN AND BARNEY J. MAGERLEIN, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167728. GABRIEL WEATHERHEAD
  167729. 10117
  167730. 11126N
  167731. 2/28/96VgTHE HOESCH SYNTHESIS: PAUL E. SPOERRI AND ADRIEN S. DUBOIS, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167732. GABRIEL WEATHERHEAD
  167733. 10118
  167734. 11127N
  167735. 2/28/96VWSELENIUM DIOXIDE OXIDATION: NORMAN RABJOHN, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167736. GABRIEL WEATHERHEAD
  167737. 10119
  167738. 11128N
  167739. 2/28/96VTTHE LEUCKART REACTION: MAURICE L. MOORE, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167740. GABRIEL WEATHERHEAD
  167741. 10120
  167742. 11129N
  167743. 2/28/96V]THE GATTERMANN KOCH REACTION:  NATHAN N. CROUNSE, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167744. GABRIEL WEATHERHEAD
  167745. 10121
  167746. 11130N
  167747. 2/28/96V
  167748. THE FRIEDEL AND CRATS REACTION WILH A!IPHATIC DIBASIC ACID ANHYDRIDES: ERNST BERLINER, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167749. GABRIEL WEATHERHEAD
  167750. 10122
  167751. 11131N
  167752. 2/28/96V
  167753. PREPARATION OF AROMATIC FLUORINE COMPOUNDS FROM DIAZONIUM FLUOBORATES: THE SCHIEMANN REACTION: ARTHUR ROE, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167754. GABRIEL WEATHERHEAD
  167755. 10123
  167756. 11132N
  167757. 2/28/96V
  167758. THE DIELS ALDER REACTION: QUINONES AND OTHER CYCLENONES:  LEWIS W. BUTZ AND ANTON W. RYTINA, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167759. GABRIEL WEATHERHEAD
  167760. 10124
  167761. 11133N
  167762. 2/28/96VNCYANOETHYLATION: HERMAN A. BRUSON, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167763. GABRIEL WEATHERHEAD
  167764. 10125
  167765. 11134N
  167766. 2/28/96V[THE SYNTHESIS OF ACETYLENES:  THOMAS L. JACOBS, ORGANIC REACTIONS VOLUME 5 (1949) A REVIEW.a
  167767. GABRIEL WEATHERHEAD
  167768. 10126
  167769. 11135N
  167770. 2/28/96VSTHE WOLF KISHNER REDUCBON:  DAVID TODD, ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167771. GABRIEL WEATHERHEAD
  167772. 10127
  167773. 11136N
  167774. 2/28/96
  167775. THE ROSENMUND REDUCTION OF ACID CHLORIDES TO ALDEHYDES:  ERICH MOSETTIG AND RALPH MOZINGO, ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167776. GABRIEL WEATHERHEAD
  167777. 10128
  167778. 11137N
  167779. 2/28/96VbSYNTHESIS OF BENZOQUINONES BY OXIDATION:  JAMES CASON, ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167780. GABRIEL WEATHERHEAD
  167781. 10129
  167782. 11138N
  167783. 2/28/96VkTHE SYNTHESIS OF BENZOINS:  WALTER S. IDE AND JOHANNES S. BUCK,.ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167784. GABRIEL WEATHERHEAD
  167785. 10130
  167786. 11139N
  167787. 2/28/96VJTHE ACYLOINS:  S. M. MCELVAIN, ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167788. GABRIEL WEATHERHEAD
  167789. 10131
  167790. 11140N
  167791. 2/28/96VsTHE PREPARATION OF AMINES BY REDUCTIVE ALKYLATION:  WILLIAM S. EMERSON, ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167792. GABRIEL WEATHERHEAD
  167793. 10132
  167794. 11141N
  167795. 2/28/96VyTHE DIELS ALDER REACTION: ETHYLENIC AND ACETYLENIC DIENOPHILES:  H. L. HOLMES ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167796. GABRIEL WEATHERHEAD
  167797. 10133
  167798. 11142N
  167799. 2/28/96VnTHE DIELS ALDER REACTION WITH MALEIC ANHYDRIDE: MILTON C. KLOETZEL ORGANIC REACTIONS VOLUME 4 (1948) A REVIEW.a
  167800. GABRIEL WEATHERHEAD
  167801. 10134
  167802. 11143N
  167803. 2/28/96VTTHE CURTIUS REACTION:  PETER A. S. SMITH ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167804. GABRIEL WEATHERHEAD
  167805. 10135
  167806. 11144N
  167807. 2/28/96VMTHE SCHMIDT REACTION:  HANS WOLFF ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167808. GABRIEL WEATHERHEAD
  167809. 10136
  167810. 11145N
  167811. 2/28/96VdTHE HOFMANN REACTION:  EVERETT S. WALLIS AND JOHN F LANE ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167812. GABRIEL WEATHERHEAD
  167813. 10137
  167814. 11146N
  167815. 2/28/96VnSUBSTITUTION AND ADDITION REACTIONS OF THIOCYANOGEN:  JOHN L. WOOD ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167816. GABRIEL WEATHERHEAD
  167817. 10138
  167818. 11147N
  167819. 2/28/96VEAZLACTONES:  H. E. CARTER ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167820. GABRIEL WEATHERHEAD
  167821. 10139
  167822. 11148N
  167823. 2/28/96
  167824. DIRECT SULFONATION OF AROMATIC HYDROCARBONS AND THEIR HALOGEN DERIVATIVES: C. M. SUTER AND ARTHUR W. WESTON ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167825. GABRIEL WEATHERHEAD
  167826. 10140
  167827. 11149N
  167828. 2/28/96VtPREPARATION OF KETENES AND KETENE DIMERS:  W E HANFORD AND JOHN C. SAUER ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167829. GABRIEL WEATHERHEAD
  167830. 10141
  167831. 11150N
  167832. 2/28/96VgTHE WILLGERODT REACTION:  MARVIN CARMACK AND M. A. SPIELMAN ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167833. GABRIEL WEATHERHEAD
  167834. 10142
  167835. 11151N
  167836. 2/28/96V~THE ACYLATION OF AROMATIC COMPOUNDS BY THE FRIEDEL CRAFTS METHOD: CHARLES C. PRICE ORGANIC REACTIONS VOLUME 3 (1946) A REVIEW.a
  167837. GABRIEL WEATHERHEAD
  167838. 10143
  167839. 11152N
  167840. 2/28/96V
  167841. THE PREPARATION OF AROMATIC ARSONIC AND ARSINIC ACIDS BY THE BART, BECHAMP, AND ROSENMUND REACTIONS:  CLIFF S. HAMILTON AND JACK F. MORGAN ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  167842. GABRIEL WEATHERHEAD
  167843. 10144
  167844. 11153N
  167845. 2/28/96
  167846. VWTHE RESOLUTION OF ALCOHOLS: A. W. INGERSOLL ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  167847. GABRIEL WEATHERHEAD
  167848. 10145
  167849. 11154N
  167850. 2/28/96VVPERIODIC ACID OXIDATION: ERNEST L. JACKSON ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  167851. GABRIEL WEATHERHEAD
  167852. 10146
  167853. 11155N
  167854. 2/28/96VxREPLACEMENT OF THE AROMATIC PRIMARY AMINO GROUP HY HYDROGEN: NATHAN KORNBLUM ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  167855. GABRIEL WEATHERHEAD
  167856. 10147
  167857. 11156N
  167858. 2/28/96V
  167859. THE PREPARATION OF UNSYMMETRICAL BIARYLS BY THE DIAZO REACTION AND THE NITROSOACETYLAMINE REACTION:  WERNER E. BACHMANN AND ROGER A. HOFFMAN ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  167860. GABRIEL WEATHERHEAD
  167861. 10148
  167862. 11157N
  167863. 2/28/96V
  167864. A. ZLATKIS AND R. E. KAISER, HPTLC HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY, ELSEVIER, NORTH HOLLAND, 1977. REDUCTIONS OF N O AND N=O AND N=N COMPOUNDS WITH NI AL ALLOY LUNN, G.; SANSONE, E. B.; KEEFER, L. K. SYNTHESIS 1104 (1985) A REVIEW.a
  167865. GABRIEL WEATHERHEAD
  167866. 10149
  167867. 11158N
  167868. 2/28/96VlW. P. WEBER AND G. W. GOKEL, PHASE TRANSFER CATALYSIS IN ORGANIC SYNTHESIS, SPRINGER VERLAG, 1977. A REVIEW.a
  167869. GABRIEL WEATHERHEAD
  167870. 10150
  167871. 11159N
  167872. 2/28/96V
  167873. J. S. PIZEY, SYNTHETIC REAGENTS, VOL. 3 (DIBORANE, 2,3 DICHLORO 5,6 DICYANOQUINONE, IODINE, LEAD TETRAACETATE), HALSTED WILEY INTERSCIENCE,  1977. A REVIEW.a
  167874. GABRIEL WEATHERHEAD
  167875. 10151
  167876. 11160N
  167877. 2/28/96V{H. PINES AND W. M. STALICK, BASE CATALYZED REACTIONS OF HYDROCARBONS AND RELATED COMPOUNDS, ACADEMIC PRESS, 1977. A REVIEW.a
  167878. GABRIEL WEATHERHEAD
  167879. 10152
  167880. 11161N
  167881. 2/28/96V]G. R. PETTIT, BIOSYNTHETIC PRODUCTS FOR CANCER CHEMOTHERAPHY, VOL. 1, PLENUM, 1977. A REVIEW.a
  167882. GABRIEL WEATHERHEAD
  167883. 10153
  167884. 11162N
  167885. 2/28/96VrW. R. NES AND M. L. MCKEAN, BIOCHEMISTRY OF STEROIDS AND OTHER ISOPRENOIDS, UNIVERSITY PARK PRESS, 1977. A REVIEW.a
  167886. GABRIEL WEATHERHEAD
  167887. 10154
  167888. 11163N
  167889. 2/28/96
  167890. VJA. MITRA, SYNTHESIS OF PROSTAGLANDINS, WILEY LNTERSCIENCE, 1977. A REVIEW.a
  167891. GABRIEL WEATHERHEAD
  167892. 10155
  167893. 11164N
  167894. 2/28/96VGJ. MANN, SECONDARY METABOLISM, OXFORD UNIVERSITY PRESS, 1977. A REVIEW.a
  167895. GABRIEL WEATHERHEAD
  167896. 10156
  167897. 11165N
  167898. 2/28/96VhD. LEDNICER AND L. A. MITSCHER, ORGANIC CHEMISTRY OF DRUG SYNTHESIS, WILEY INTERSCIENCE, 1977. A REVIEW.a
  167899. GABRIEL WEATHERHEAD
  167900. 10157
  167901. 11166N
  167902. 2/28/96VvH. KWART AND K. KING, D ORBITALS IN THE CHEMISTRY OF SILICON, PHOSPHORUS, AND SULFUR, SPRINGER VERLAG, 1977. A REVIEW.a
  167903. GABRIEL WEATHERHEAD
  167904. 10158
  167905. 11167N
  167906. 2/28/96VVR. A. JONES AND G. P. DEAN, THE CHEMISTRY OF PYRROLES, ACADEMIC PRESS, 1977. A REVIEW.a
  167907. GABRIEL WEATHERHEAD
  167908. 10159
  167909. 11168N
  167910. 2/28/96VyY. IZUMI AND A. TAI, STEREO DIFFERENTIATING REACTIONS
  167911. THE NATURE OF ASYMMETRIC REACTIONS, ACADEMIC PRESS, 1977. A REVIEW.a
  167912. GABRIEL WEATHERHEAD
  167913. 10160
  167914. 11169N
  167915. 2/28/96
  167916. %VxT. L. HO, THE HARD AND SOFT ACIDS AND BASES PRINCIPLE. APPLICATION TO ORGANIC CHEMISTRY, ACADEMIC PRESS, 1977. A REVIEW.a
  167917. GABRIEL WEATHERHEAD
  167918. 10161
  167919. 11170N
  167920. 2/28/96VNA. J. FRY, SYNTHETIC ORGANIC ELECTROCHEMISTRY, HARPER AND ROW, 1977. A REVIEW.a
  167921. GABRIEL WEATHERHEAD
  167922. 10162
  167923. 11171N
  167924. 2/28/96V`I. FLEMING, FRONTIER ORBITALS AND ORGANIC CHEMICAL REACTIONS, WILEY LNTERSCIENCE, 1976 A REVIEW.a
  167925. GABRIEL WEATHERHEAD
  167926. 10163
  167927. 11172N
  167928. 2/28/96VCH. C. BROWN, THE NON CLASSICAL ION PROBLEM, PLENUM, 1977. A REVIEW.a
  167929. GABRIEL WEATHERHEAD
  167930. 10164
  167931. 11173N
  167932. 2/28/96VTJ. S. BINDRA AND R. BINDRA, PROSTAGLANDIN SYNTHESIS, ACADEMIC PRESS, 1977. A REVIEW.a
  167933. GABRIEL WEATHERHEAD
  167934. 10165
  167935. 11174N
  167936. 2/28/96VpW. L. F. ARMAREGO, STEREOCHEMISTRY OF HETEROCYCLIC COMPOUNDS, PARTS 1 AND 2, WILEY LNTERSCIENCE, 1977. A REVIEW.a
  167937. GABRIEL WEATHERHEAD
  167938. 10166
  167939. 11175N
  167940. 2/28/96
  167941. R. V. STEVENS, ALKALOID SYNTHESIS. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. III, J. APSIMON, ED., WILEY LNTERSCIENCE, 1977 A REVIEW.a
  167942. GABRIEL WEATHERHEAD
  167943. 10167
  167944. 11176N
  167945. 2/28/96V
  167946. J. P. KUTNEY, THE SYNTHESIS OF INDOLE ALKALOIDS. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. III, J. APSIMON, ED., WILEY LNTERSCIENCE, 1977 A REVIEW.a
  167947. GABRIEL WEATHERHEAD
  167948. 10168
  167949. 11177N
  167950. 2/28/96V
  167951. T. KAMETANI, THE TOTAL SYNTHESIS OF ISOQUINOLINE ALKALOIDS. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. III, J. APSIMON, ED., WILEY LNTERSCIENCE, 1977 A REVIEW.a
  167952. GABRIEL WEATHERHEAD
  167953. 10169
  167954. 11178N
  167955. 2/28/96VzE. SCHACHT, HYPOLIPIDEMIC ARYLOXYACETIC ACIDS, 72, 99 (1977). TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG, 1977 A REVIEW.a
  167956. GABRIEL WEATHERHEAD
  167957. 10170
  167958. 11179N
  167959. 2/28/96V
  167960. D. ORTH AND H. E. RADUZ, SYNTHESES AND ACTIVITY OF HETEROPROSTANOIDS, 72, 51 (1977). TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG, 1977 A REVIEW.a
  167961. GABRIEL WEATHERHEAD
  167962. 10171
  167963. 11180N
  167964. 2/28/96V
  167965. W. WEHRLI, ANSAMYCINS
  167966. CHEMISTRY, BIOSYNTHESIS AND ACTIVITY, 72, 21(1977). TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG, 1977 A REVIEW.a
  167967. GABRIEL WEATHERHEAD
  167968. 10172
  167969. 11181N
  167970. 2/28/96V
  167971. N. D. EPIOTIS, W. R. CHERRY, S. SHAIK, R. YATES, AND F. BERNARDI, STRUCTURAL THEORY OF ORGANIC CHEMISTRY, 70,1 (1977). TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG, 1977 A REVIEW.a
  167972. GABRIEL WEATHERHEAD
  167973. 10173
  167974. 11182N
  167975. 2/28/96V
  167976. D. M. STURMER SYNTHESES AND PROPERTIES OF CYANINE AND RELATED DYES, 441. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  167977. GABRIEL WEATHERHEAD
  167978. 10174
  167979. 11183N
  167980. 2/28/96V
  167981. A. J. FRITSCH, BORAZAROMATIC COMPOUNDS, 381. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  167982. GABRIEL WEATHERHEAD
  167983. 10175
  167984. 11184N
  167985. 2/28/96V
  167986. K. T. POTTS, HETEROPENTALENES, 317. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  167987. GABRIEL WEATHERHEAD
  167988. 10176
  167989. 11185N
  167990. 2/28/96V
  167991. R. D. HAMILTON AND E. CAMPAIGNE, DITHIOLE AND DITHIOLIUM SYSTEMS, SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  167992. GABRIEL WEATHERHEAD
  167993. 10177
  167994. 11186N
  167995. 2/28/96V
  167996. A. TAURINS, THE CHEMISTRY OF CYCLAZINES, 245. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  167997. GABRIEL WEATHERHEAD
  167998. 10178
  167999. 11187N
  168000. 2/28/96
  168001. G. MAURY, AZAINDOLIZINE SYSTEMS HAVING MORE THAN ONE NITROGEN ATOM IN THE 6 MEMBERED RING, 179. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168002. GABRIEL WEATHERHEAD
  168003. 10179
  168004. 11188N
  168005. 2/28/96V
  168006. H. L. BLEWITT, INDOLIZINE AND AZA DERIVATIVES WITH ADDITIONAL NITROGENS IN THE 5 MEMBERED RING, 117. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A.WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168007. GABRIEL WEATHERHEAD
  168008. 10180
  168009. 11189N
  168010. 2/28/96V
  168011. J. P. PAOLINI, 5,5 SYSTEMS WITH A BRIDGEHEAD NITROGEN ATOM, 1. SPECIAL TOPICS IN HETEROCYCLIC CHEMISTRY, A. WEISSBERGER AND E. C. TAYLOR, EDS. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168012. GABRIEL WEATHERHEAD
  168013. 10181
  168014. 11190N
  168015. 2/28/96
  168016. J. E. BALDWIN, THERMALLY FORBIDDEN REACTIONS. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 2 A REVIEW.a
  168017. GABRIEL WEATHERHEAD
  168018. 10182
  168019. 11191N
  168020. 2/28/96V
  168021. K. N. HOUK, APPLICATIONS OF FRONTIER MOLECULAR ORBITAL THEORY TO PERICYCLIC REACTIONS PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 2 A REVIEW.a
  168022. GABRIEL WEATHERHEAD
  168023. 10183
  168024. 11192N
  168025. 2/28/96V
  168026. W. L. MOCK, CHELETROPIC REACTIONS. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 2 A REVIEW.a
  168027. GABRIEL WEATHERHEAD
  168028. 10184
  168029. 11193N
  168030. 2/28/96V
  168031. L. GHOSEZ AND M. J. O'DONNELL, PERICYCLIC REACTIONS OF CUMULENES. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 2 A REVIEW.a
  168032. GABRIEL WEATHERHEAD
  168033. 10185
  168034. 11194N
  168035. 2/28/96
  168036. T. S. SORENSON AND A. RAUK, CARBOCATIONS. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 2 A REVIEW.a
  168037. GABRIEL WEATHERHEAD
  168038. 10186
  168039. 11195N
  168040. 2/28/96V
  168041. S. W. STALEY, PERICYCLIC REACTIONS OF CARBANIONS. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 1 A REVIEW.a
  168042. GABRIEL WEATHERHEAD
  168043. 10187
  168044. 11196N
  168045. 2/28/96V
  168046. W. M. JONES AND U. H. BRINKER, SOME PERICYCLIC REACTIONS OF CARBENES. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 1 A REVIEW.a
  168047. GABRIEL WEATHERHEAD
  168048. 10188
  168049. 11197N
  168050. 2/28/96V
  168051. H. E. ZIMMERMAN, THE MOBIUS HUCKEL TREATMENT OF ORGANIC SYSTEMS AND REACTIONS AND MO FOLLOWING AS A TECHNIQUE IN ORGANIC CHEMISTRY. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 1 A REVIEW.a
  168052. GABRIEL WEATHERHEAD
  168053. 10189
  168054. 11198N
  168055. 2/28/96
  168056. R. E. LEHR AND A. P. MARCHAND, OPERATIONAL CRITERIA FOR EVALUATION OF CONCERTEDNESS IN POTENTIAL PERICYCLIC REACTIONS. PERICYCLIC REACTIONS, A. P. MARCHAND AND R. E. LEHR, EDS., ACADEMIC PRESS, 1977, VOLUME 1 A REVIEW.a
  168057. GABRIEL WEATHERHEAD
  168058. 10190
  168059. 11199N
  168060. 2/28/96V
  168061. M. F. FARONA, HOMOGENEOUS CATALYSIS BY ARENE GROUP VIB TRICARBONYLS. ORGANOMETALLIC REACTIONS AND SYNTHESES, VOL. 6, E. 1. BECKER AND M. TSUTSUI, EDS., PLENUM, 1977 A REVIEW.a
  168062. GABRIEL WEATHERHEAD
  168063. 10191
  168064. 11200N
  168065. 2/28/96V
  168066. R. N. GRIMES, REACTIONS OF METALLOCARBORANES. ORGANOMETALLIC REACTIONS AND SYNTHESES, VOL. 6, E. 1. BECKER AND M. TSUTSUI, EDS., PLENUM, 1977 A REVIEW.a
  168067. GABRIEL WEATHERHEAD
  168068. 10192
  168069. 11201N
  168070. 2/28/96V
  168071. C. U. PITTMAN, JR., VINYL POLYMERIZATION OF ORGANIC MONOMERS CONTAINING TRANSITION METALS. ORGANOMETALLIC REACTIONS AND SYNTHESES, VOL. 6, E. 1. BECKER AND M. TSUTSUI, EDS., PLENUM, 1977 A REVIEW.a
  168072. GABRIEL WEATHERHEAD
  168073. 10193
  168074. 11202N
  168075. 2/28/96
  168076. J. HALPERN, CATALYSIS OF SYMMETRY RESTRICTED REACTIONS BY TRANSITION METAL COMPOUNDS, 705. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168077. GABRIEL WEATHERHEAD
  168078. 10194
  168079. 11203N
  168080. 2/28/96V
  168081. J. F. HARROD AND A. J. CHALK, HYDROSILATION CATALYZED BY GROUP VLLL COMPLEXES, 673. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168082. GABRIEL WEATHERHEAD
  168083. 10195
  168084. 11204N
  168085. 2/28/96V
  168086. E. S. BROWN, ADDITION OF HYDROGEN CYANIDE TO OLEFINS, 655. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168087. GABRIEL WEATHERHEAD
  168088. 10196
  168089. 11205N
  168090. 2/28/96V
  168091. J. TSUJI, DECARBONYLATION REACTIONS USING TRANSITION METAL COMPOUNDS, 595. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168092. GABRIEL WEATHERHEAD
  168093. 10197
  168094. 11206
  168095. 2/28/96V
  168096. H. ALPER, ORGANIC SYNTHESES WITH IRON PENTACARBONYL, 545. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168097. GABRIEL WEATHERHEAD
  168098. 10198
  168099. 11207N
  168100. 2/28/96V
  168101. T. A. WEIL, L. CASSAR, AND M. FOA, CARBONYLATION OF ORGANIC HALIDES, 517. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168102. GABRIEL WEATHERHEAD
  168103. 10199
  168104. 11208N
  168105. 2/28/96
  168106. P. PINO AND G. BRACA, CARBON MONOXIDE ADDITION TO ACETYLENIC SUBSTRATES: SYNTHESIS OF QUINONES, ACRYLIC AND SUCCINIC ACIDS AND THEIR DERIVATIVES, 419. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.
  168107. GABRIEL WEATHERHEAD
  168108. 10200
  168109. 11209N
  168110. 2/28/96
  168111. G. P. CHIUSOLI AND L. CASSAR, ORGANIC SYNTHESES VIA ALLYLIC COMPLEXES OF METAL CARBONYLS, 297. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168112. GABRIEL WEATHERHEAD
  168113. 10201
  168114. 11210N
  168115. 2/28/96V
  168116. P. PINO, F. PIACENTI, AND M. BIANCHI, HYDROCARBOXYLATION OF OLEFINS WITH CARBON MONOXIDE AND RELATED REACTIONS, 233. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168117. GABRIEL WEATHERHEAD
  168118. 10202
  168119. 11211N
  168120. 2/28/96
  168121. P. PINO, F. PIACENTI, AND M. BIANCHI, REACTIONS OF CARBON MONOXIDE AND HYDROGEN WITH OLEFINIC SUBSTRATES: THE HYDROFORMYLATION (OXO) REACTION, 43. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.
  168122. GABRIEL WEATHERHEAD
  168123. 10203
  168124. 11212N
  168125. 2/28/96
  168126. F. PIACENTI AND M. BIANCHI, CARBONYLATION OF SATURATED OXYGENATED COMPOUNDS, 1. ORGANIC SYNTHESES VIA METAL CARBONYLS, VOL. 2, I. WENDER AND P. PINO, EDS., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168127. GABRIEL WEATHERHEAD
  168128. 10204
  168129. 11213N
  168130. 2/28/96VyE. T. KAISER, REACTIONS OF SULFONATE AND SULFATE ESTERS. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168131. GABRIEL WEATHERHEAD
  168132. 10205
  168133. 11214N
  168134. 2/28/96V{S. OAE AND N. KUNIEDA, SULFINIC ACIDS AND SULFINIC ESTERS. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168135. GABRIEL WEATHERHEAD
  168136. 10206
  168137. 11215N
  168138. 2/28/96V
  168139. W. E. TRUCE, T. C. KLINGER, AND W. W. BRAND, SULFONES AND SULFOXIMINES. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168140. GABRIEL WEATHERHEAD
  168141. 10207
  168142. 11216N
  168143. 2/28/96VdC. J. M. STIRLING, SULFONIUM SALTS. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168144. GABRIEL WEATHERHEAD
  168145. 10208
  168146. 11217N
  168147. 2/28/96
  168148. UVeS. OAE, SULFOXIDES AND SULFILIMINES. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168149. GABRIEL WEATHERHEAD
  168150. 10209
  168151. 11218N
  168152. 2/28/96VgL. FIELD, DISULFIDES AND POLYSULFIDES. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168153. GABRIEL WEATHERHEAD
  168154. 10210
  168155. 11219N
  168156. 2/28/96VUW. TAGAKI, SULFIDES. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168157. GABRIEL WEATHERHEAD
  168158. 10211
  168159. 11220N
  168160. 2/28/96VQA.OHNO, THIONES. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168161. GABRIEL WEATHERHEAD
  168162. 10212
  168163. 11221N
  168164. 2/28/96V\A. OHNO AND S. OAE, THIOLS. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168165. GABRIEL WEATHERHEAD
  168166. 10213
  168167. 11222N
  168168. 2/28/96VdM. PORTER, VULCANIZATION OF RUBBER. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168169. GABRIEL WEATHERHEAD
  168170. 10214
  168171. 11223N
  168172. 2/28/96
  168173. [VnR. MAYER, ELEMENTAL SULFUR AND ITS REACTIONS. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168174. GABRIEL WEATHERHEAD
  168175. 10215
  168176. 11224N
  168177. 2/28/96V\H. A. BENT, SULFUR BONDING. ORGANIC CHEMISTRY OF SULFUR, S. OAE, ED., PLENUM, 1977 A REVIEW.a
  168178. GABRIEL WEATHERHEAD
  168179. 10216
  168180. 11225N
  168181. 2/28/96V
  168182. F. J. SCHMITZ, UNCOMMON MARINE STEROIDS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 1, P. J. SCHEUER, ED., ACADEMIC PRESS, 1977 A REVIEW.a
  168183. GABRIEL WEATHERHEAD
  168184. 10217
  168185. 11226N
  168186. 2/28/96V
  168187. L. MINALE, TERPENOIDS FROM MARINE SPONGES. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 1, P. J. SCHEUER, ED., ACADEMIC PRESS, 1977 A REVIEW.a
  168188. GABRIEL WEATHERHEAD
  168189. 10218
  168190. 11227N
  168191. 2/28/96V
  168192. J. D. MARTIN AND J. DARIAS, ALGAL SESQUITERPENOIDS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 1, P. J. SCHEUER, ED., ACADEMIC PRESS, 1977 A REVIEW.a
  168193. GABRIEL WEATHERHEAD
  168194. 10219
  168195. 11228N
  168196. 2/28/96V
  168197. R. E. MOORE, ALGAL NON LSOPRENOIDS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 1, P. J. SCHEUER, ED., ACADEMIC PRESS, 1977 A REVIEW.a
  168198. GABRIEL WEATHERHEAD
  168199. 10220
  168200. 11229N
  168201. 2/28/96V
  168202. Y. SHIMIZU, DINOFLAGELLATE TOXINS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES, VOL. 1, P. J. SCHEUER, ED., ACADEMIC PRESS, 1977 A REVIEW.a
  168203. GABRIEL WEATHERHEAD
  168204. 10221
  168205. 11230N
  168206. 2/28/96V
  168207. G. P. ELLIS, CHROMONES AND DERIVATIVES, 455. CHROMENES, CHROMANONES, AND CHROMONES, G. P. ELLIS, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168208. GABRIEL WEATHERHEAD
  168209. 10222
  168210. 11231N
  168211. 2/28/96V
  168212. I. M. LOCKHART, CHROMANOLS AND CHROMANONES, 141. CHROMENES, CHROMANONES, AND CHROMONES, G. P. ELLIS, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168213. GABRIEL WEATHERHEAD
  168214. 10223
  168215. 11232N
  168216. 2/28/96
  168217. E. E. SCHWEIZER AND D. MEEDER NYCZ, 2H  AND 4H L BENZOPYRANS, 11. CHROMENES, CHROMANONES, AND CHROMONES, G. P. ELLIS, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE, 1977 A REVIEW.a
  168218. GABRIEL WEATHERHEAD
  168219. 10224
  168220. 11233N
  168221. 2/28/96V
  168222. J. A. ELVIDGE AND N. R. BAROT, IMIDINES AND DIAMIDIDES (1,3,5 TRIAZAPENTADIENES), 1167. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168223. GABRIEL WEATHERHEAD
  168224. 10225
  168225. 11234N
  168226. 2/28/96V
  168227. J. K. STILLE AND D. E. JAMES, TRANSITION METAL CATALYZED CARBONYLATION OF OLEFINS, 1099. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168228. GABRIEL WEATHERHEAD
  168229. 10226
  168230. 11235N
  168231. 2/28/96V
  168232. P. M. HENRY AND G. L. LANGE, OXIDATION OF C=C AND C=N GROUPS, 965. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168233. GABRIEL WEATHERHEAD
  168234. 10227
  168235. 11236N
  168236. 2/28/96
  168237. N. CALDERON, THE OLEFIN METATHESIS REACTION, 913. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168238. GABRIEL WEATHERHEAD
  168239. 10228
  168240. 11237N
  168241. 2/28/96V
  168242. G. H. SCHMID AND D. G. GARRATT, ELECTROPHILIC ADDITIONS TO CARBON CARBON DOUBLE BONDS, 725. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168243. GABRIEL WEATHERHEAD
  168244. 10229
  168245. 11238N
  168246. 2/28/96V
  168247. K. B. BECKER AND C. A. GROB, THE FORMATION OF UNSATURATED GROUPS BY HETEROLYTIC FRAGMENTATION, 653. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168248. GABRIEL WEATHERHEAD
  168249. 10230
  168250. 11239N
  168251. 2/28/96V
  168252. A. P. MARCHAND, REACTIONS OF CARBENES WITH X=Y GROUPS, 533. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168253. GABRIEL WEATHERHEAD
  168254. 10231
  168255. 11240N
  168256. 2/28/96
  168257. G. BIANCHI, C. DE MICHELI, AND R. GANDOLFI, 1,3 DIPOLAR CYCLOADDITIONS INVOLVING X=Y GROUPS, 369. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168258. GABRIEL WEATHERHEAD
  168259. 10232
  168260. 11241N
  168261. 2/28/96V
  168262. A. J. FRY AND R. G. REED, THE ELECTROCHEMISTRY OF X=Y GROUPS, 331. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168263. GABRIEL WEATHERHEAD
  168264. 10233
  168265. 11242N
  168266. 2/28/96V
  168267. A. F. COCKERILL AND R. G. HARRISON, MECHANISMS OF ELIMINATION AND ADDITION REACTIONS INVOLVING THE X=Y GROUP, 149. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168268. GABRIEL WEATHERHEAD
  168269. 10234
  168270. 11243N
  168271. 2/28/96V
  168272. R. SHAW, THERMOCHEMISTRY OF X=Y GROUPS, 131. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168273. GABRIEL WEATHERHEAD
  168274. 10235
  168275. 11244N
  168276. 2/28/96
  168277. J. P. VAN METER, LIQUID CRYSTALS WITH X=Y GROUPS, 93. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168278. GABRIEL WEATHERHEAD
  168279. 10236
  168280. 11245N
  168281. 2/28/96V
  168282. O. EXNER, DIPOLE MOMENTS, CONFIGURATIONS AND CONFORMATIONS OF MOLECULES CONTAINING X=Y GROUPS, 1. CHEMISTRY OF DOUBLE BONDED FUNCTIONAL GROUPS, S. PATAI, ED., WILEY INTERSCIENCE, 1977 A REVIEW.a
  168283. GABRIEL WEATHERHEAD
  168284. 10237
  168285. 11246N
  168286. 2/28/96V
  168287. C. N. C. DREY, CHEMISTRY AND BIOCHEMISTRY OF BETA AMINO ACIDS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 4, B. WEINSTEIN, ED., MARCEL DEKKER, 1977 A REVIEW.a
  168288. GABRIEL WEATHERHEAD
  168289. 10238
  168290. 11247N
  168291. 2/28/96V
  168292. A. B. MAUGER, THE CHEMISTRY OF CYCLIC ALPHA IMINO ACIDS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 4, B. WEINSTEIN, ED., MARCEL DEKKER, 1977 A REVIEW.a
  168293. GABRIEL WEATHERHEAD
  168294. 10239
  168295. 11248N
  168296. 2/28/96
  168297. J. C. POWERS, HALOKETONE INHIBITORS OF PROTEOLYTIC ENZYMES. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 4, B. WEINSTEIN, ED., MARCEL DEKKER, 1977 A REVIEW.a
  168298. GABRIEL WEATHERHEAD
  168299. 10240
  168300. 11249N
  168301. 2/28/96V
  168302. J. H. JONES, SEQUENTIAL POLYPEPTIDE SYNTHESIS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 4, B. WEINSTEIN, ED., MARCEL DEKKER, 1977 A REVIEW.a
  168303. GABRIEL WEATHERHEAD
  168304. 10241
  168305. 11250N
  168306. 2/28/96V
  168307. J. S. DAVIES, OCCURRENCE AND BIOSYNTHESIS OF D AMINO ACIDS. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, VOL. 4, B. WEINSTEIN, ED., MARCEL DEKKER, 1977 A REVIEW.a
  168308. GABRIEL WEATHERHEAD
  168309. 10242
  168310. 11251N
  168311. 2/28/96V
  168312. A. J. WILLI, KINETIC CARBON AND OTHER ISOTOPE EFFECTS IN CLEAVAGE AND FORMATION OF BONDS TO CARBON, 237. CARBON 13 IN ORGANIC CHEMISTRY, E. BUNCEL AND C. E. LEE, EDS. (ISOTOPES IN ORGANIC CHEMISTRY), ELSEVIER, 1977. A REVIEW.a
  168313. GABRIEL WEATHERHEAD
  168314. 10243
  168315. 11252N
  168316. 2/28/96V
  168317. A. S. PERLIN, 13C NMR IN PROBLEMS OF STEREOCHEMISTRY, 171. CARBON 13 IN ORGANIC CHEMISTRY, E. BUNCEL AND C. E. LEE, EDS. (ISOTOPES IN ORGANIC CHEMISTRY), ELSEVIER, 1977. A REVIEW.a
  168318. GABRIEL WEATHERHEAD
  168319. 10244
  168320. 11253N
  168321. 2/28/96V
  168322. G. KUNESCH AND C. POUPAT, BIOSYNTHETIC STUDIES WITH 13C PRECURSORS, 105. CARBON 13 IN ORGANIC CHEMISTRY, E. BUNCEL AND C. E. LEE, EDS. (ISOTOPES IN ORGANIC CHEMISTRY), ELSEVIER, 1977. A REVIEW.a
  168323. GABRIEL WEATHERHEAD
  168324. 10245
  168325. 11254N
  168326. 2/28/96V
  168327. J. HINTON, M. OKA, AND A. FRY, 13C NMR METHODOLOGY AND MECHANISTIC APPLICATIONS, 41. CARBON 13 IN ORGANIC CHEMISTRY, E. BUNCEL AND C. E. LEE, EDS. (ISOTOPES IN ORGANIC CHEMISTRY), ELSEVIER, 1977. A REVIEW.a
  168328. GABRIEL WEATHERHEAD
  168329. 10246
  168330. 11255N
  168331. 2/28/96V
  168332. G. E. DUNN, 13C KINETIC ISOTOPE EFFECTS IN DECARBOXYLATION, 1. CARBON 13 IN ORGANIC CHEMISTRY, E. BUNCEL AND C. E. LEE, EDS. (ISOTOPES IN ORGANIC CHEMISTRY), ELSEVIER, 1977. A REVIEW.a
  168333. GABRIEL WEATHERHEAD
  168334. 10247
  168335. 11256N
  168336. 2/28/96V}W. L. DUAX, C. M. WEEKS, AND D. C. ROHRER, CRYSTAL STRUCTURES OF STEROIDS, 9, 271 (1976). TOPICS IN STEREOCHEMISTRY A REVIEW.a
  168337. GABRIEL WEATHERHEAD
  168338. 10248
  168339. 11257N
  168340. 2/28/96VoJ. DALE, MULTISTEP CONFORMATIONAL INTERCONVERSION MECHANISMS, 9,199 (1976). TOPICS IN STEREOCHEMISTRY A REVIEW.a
  168341. GABRIEL WEATHERHEAD
  168342. 10249
  168343. 11258N
  168344. 2/28/96V
  168345. O. HOFER, THE LANTHANIDE INDUCED SHIFT TECHNIQUE: APPLICATIONS IN CONFORMATIONAL ANALYSIS, 9,111(1976). TOPICS IN STEREOCHEMISTRY A REVIEW.a
  168346. GABRIEL WEATHERHEAD
  168347. 10250
  168348. 11259N
  168349. 2/28/96V~M. M. GREEN, MASS SPECTROMETRY AND THE STEREOCHEMISTRY OF ORGANIC MOLECULES, 9, 35 (1976). TOPICS IN STEREOCHEMISTRY A REVIEW.a
  168350. GABRIEL WEATHERHEAD
  168351. 10251
  168352. 11260N
  168353. 2/28/96VjS. F. MASON, THE FOUNDATIONS OF CLASSICAL STEREOCHEMISTRY, 9, 1(1976). TOPICS IN STEREOCHEMISTRY A REVIEW.a
  168354. GABRIEL WEATHERHEAD
  168355. 10252
  168356. 11261N
  168357. 2/28/96
  168358. P. D. ELLIS AND R. DITCHFIELD, THEORY OF INDIRECT NUCLEAR SPIN SPIN COUPLING CONSTANTS WITH APPLICATIONS TO CARBON 13 NMR, 2, 434 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168359. GABRIEL WEATHERHEAD
  168360. 10253
  168361. 11262N
  168362. 2/28/96VqJ. W. COOPER THE COMPUTER IN FOURIER TRANSFORM NMR, 2, 392 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168363. GABRIEL WEATHERHEAD
  168364. 10254
  168365. 11263N
  168366. 2/28/96V
  168367. F. W. WEHRLI, ORGANIC STRUCTURE ASSIGNMENTS USING 13C SPIN RELAXATION DATA, 2, 343 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168368. GABRIEL WEATHERHEAD
  168369. 10255
  168370. 11264N
  168371. 2/28/96V
  168372. O. A. GANSOW AND W. D. VERNON, CARBON 13 NMR STUDIES OF ORGANOMETALLIC AND TRANSITION METAL COMPLEX COMPOUNDS, 2, 270 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168373. GABRIEL WEATHERHEAD
  168374. 10256
  168375. 11265N
  168376. 2/28/96
  168377. R. A. KOMOROSKI, I. R. PEAT, AND G. C. LEVY, 13C NMR STUDIES OF BIOPOLYMERS, 2,180 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168378. GABRIEL WEATHERHEAD
  168379. 10257
  168380. 11266N
  168381. 2/28/96V
  168382. A. G. MCLNNES, J. A. WALTER, J. L. C. WRIGHT, AND L. C. VINING, 13C NMR BIOSYNTHETIC STUDIES, 2,126 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168383. GABRIEL WEATHERHEAD
  168384. 10258
  168385. 11267N
  168386. 2/28/96
  168387. E. WENKERT, B. L. BUCKWALTER, I. R. BURFITT, M. J. GASIC, H. E. GOTTLIEB, E. W. HAGAMAN, F. M. SCHELL, P. M. WOVKULICH, AND A. ZHELEBVA, CARBON 13 NMR SPECTROSCOPY OF NATURALLY OCCURRING SUBSTANCES, 2, 81(1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.
  168388. GABRIEL WEATHERHEAD
  168389. 10259
  168390. 11268N
  168391. 2/28/96V
  168392. R. DESLAURIERS AND I. C. P. SMITH, CONFORMATION AND STRUCTURE OF PEPTIDES, 2, 2 (1976). TOPICS IN CARBON 13 NMR SPECTROSCOPY A REVIEW.a
  168393. GABRIEL WEATHERHEAD
  168394. 10260
  168395. 11269N
  168396. 2/28/96
  168397. VhC. A. RAMSDEN, MESOMERIC BETAINE DERIVATIVES OF HETEROPENTALENES, 33, 3203 (1977). TETRAHEDRON A REVIEW.a
  168398. GABRIEL WEATHERHEAD
  168399. 10261
  168400. 11270N
  168401. 2/28/96V[N. S. ZEFIROV, THE PROBLEM OF CONFORMATIONAL EFFECTS 33, 3193 (1977). TETRAHEDRON A REVIEW.a
  168402. GABRIEL WEATHERHEAD
  168403. 10262
  168404. 11271N
  168405. 2/28/96V
  168406. C. MORIN AND R. BEUGELMANS, ACTION OF HYDROXYLAMINE HYDRAZINE AND THEIR DERIVATIVES ON GAMMA PYRONES (IN FRENCH), 33, 3183 (1977). TETRAHEDRON A REVIEW.a
  168407. GABRIEL WEATHERHEAD
  168408. 10263
  168409. 11272N
  168410. 2/28/96VxT. G. BACK, SYNTHESIS OF MACROCYCLIC LACTONES. APPROACHES TO MACROLIDE ANTIBIOTICS, 33, 3041(1977) TETRAHEDRON A REVIEW.a
  168411. GABRIEL WEATHERHEAD
  168412. 10264
  168413. 11273N
  168414. 2/28/96V
  168415. R. A. FIRESTONE, DIRADICAL MECHANISM FOR 1,3 DIPOLAR CYCLOADDITIONS AND RELATED PERICYCLIC REACTIONS, 33, 3009 (1977) TETRAHEDRON A REVIEW.a
  168416. GABRIEL WEATHERHEAD
  168417. 10265
  168418. 11274N
  168419. 2/28/96
  168420. VKT. MATSUURA, BIOMIMETIC OXYGENATION, 33, 2869 (1977). TETRAHEDRON A REVIEW.a
  168421. GABRIEL WEATHERHEAD
  168422. 10266
  168423. 11275N
  168424. 2/28/96VyL. M. JACKMANN AND B. C. LANGE, STRUCTURE AND REACTIVITY OF ALKALI METAL ENOLATES, 33, 2737 (1977). TETRAHEDRON A REVIEW.a
  168425. GABRIEL WEATHERHEAD
  168426. 10267
  168427. 11276N
  168428. 2/28/96VpS. J. WILEN, A. COLLET, AND J. JACQUES, STRATEGIES IN OPTICAL RESOLUTION, 33, 2725 (1977). TETRAHEDRON A REVIEW.a
  168429. GABRIEL WEATHERHEAD
  168430. 10268
  168431. 11277N
  168432. 2/28/96VgB. M. TROST, ORGANOPALLADIUM INTERMEDIATES IN ORGANIC SYNTHESIS, 33, 2615 (1977). TETRAHEDRON A REVIEW.a
  168433. GABRIEL WEATHERHEAD
  168434. 10269
  168435. 11278N
  168436. 2/28/96VhD. BRYCE SMITH AND A. GILBERT, ORGANIC PHOTOCHEMISTRY OF BENZENE, 33, 2459 (1977). TETRAHEDRON A REVIEW.a
  168437. GABRIEL WEATHERHEAD
  168438. 10270
  168439. 11279N
  168440. 2/28/96V[S. OAE AND N. FURUKAWA, EI REACTIONS OF SULFILIMINES 33, 2359 (1977). TETRAHEDRON A REVIEW.a
  168441. GABRIEL WEATHERHEAD
  168442. 10271
  168443. 11280N
  168444. 2/28/96
  168445. VlH. C. BROWN AND E. NEGISHI, BORAHETEROCYCLES VIA CYCLIC HYDROBORATION, 33, 2331(1977). TETRAHEDRON A REVIEW.a
  168446. GABRIEL WEATHERHEAD
  168447. 10272
  168448. 11281N
  168449. 2/28/96VxT. M. HARRIS AND C. M. HARRIS, SYNTHESIS OF POLYKETIDE AROMATIC NATURAL PRODUCTS, 33, 2159 (1977). TETRAHEDRON A REVIEW.a
  168450. GABRIEL WEATHERHEAD
  168451. 10273
  168452. 11282N
  168453. 2/28/96V^P. D. MAGNUS, RECENT DEVELOPMENTS IN SULFONE CHEMISTRY, 33, 2019 (1977). TETRAHEDRON A REVIEW.a
  168454. GABRIEL WEATHERHEAD
  168455. 10274
  168456. 11283N
  168457. 2/28/96VYC. A. HENRICK, SYNTHESIS OF INSECT SEX PHEROMONES, 33, 1845 (1977). TETRAHEDRON A REVIEW.a
  168458. GABRIEL WEATHERHEAD
  168459. 10275
  168460. 11284N
  168461. 2/28/96V[S. M. HECHT, ISOMERIC TRNA'S IN PROTEIN BIOSYNTHESIS 33, 1671 (1977). TETRAHEDRON A REVIEW.a
  168462. GABRIEL WEATHERHEAD
  168463. 10276
  168464. 11285N
  168465. 2/28/96V_D. J. ABERHART, BIOSYNTHESIS OF BETA LACTAM ANTIBIOTICS, 33, 1545 (1977). TETRAHEDRON A REVIEW.a
  168466. GABRIEL WEATHERHEAD
  168467. 10277
  168468. 11286N
  168469. 2/28/96
  168470. VYD. J. FAULKNER, MARINE NATURAL PRODUCTS CHEMISTRY, 33, 1421 (1977). TETRAHEDRON A REVIEW.a
  168471. GABRIEL WEATHERHEAD
  168472. 10278
  168473. 11287N
  168474. 2/28/96VNK. C. NICOLAOU, SYNTHESIS OF MACROLIDES, 33, 683 (1977). TETRAHEDRON A REVIEW.a
  168475. GABRIEL WEATHERHEAD
  168476. 10279
  168477. 11288N
  168478. 2/28/96VlK. G. LEWIS AND C. L. MULQUINEY, FORMATION AND USE OF STENHOUSE SALTS, 33, 463 (1977). TETRAHEDRON A REVIEW.a
  168479. GABRIEL WEATHERHEAD
  168480. 10280
  168481. 11289N
  168482. 2/28/96V^R. ROSSI, SYNTHESIS OF ACHIRAL COMPONENTS OF INSECT PHEROMONES, 1977, 817. SYNTHESIS A REVIEW.a
  168483. GABRIEL WEATHERHEAD
  168484. 10281
  168485. 11290N
  168486. 2/28/96V`L. A. SLOTIN, METHODS OF PHOSPHORYLATION OF BIOLOGICAL MOLECULES, 1977, 737. SYNTHESIS A REVIEW.a
  168487. GABRIEL WEATHERHEAD
  168488. 10282
  168489. 11291N
  168490. 2/28/96VSD. R. ADAMS AND S. P. BHATNAGAR, THE PRINS REACTION, 1977, 661. SYNTHESIS A REVIEW.a
  168491. GABRIEL WEATHERHEAD
  168492. 10283
  168493. 11292N
  168494. 2/28/96
  168495. VhG. B. BENNETT, THE CLAISEN REARRANGEMENT IN ORGANIC SYNTHESIS, 1967 1977, 1977, 589. SYNTHESIS A REVIEW.a
  168496. GABRIEL WEATHERHEAD
  168497. 10284
  168498. 11293N
  168499. 2/28/96V
  168500. E. M. KAISER, J. D. PETTY, AND P. L. A. KNUTSON POLYALKALIMETAL DERIVATIVES OF HETEROFUNCTIONAL ORGANIC MOLECULES, 1977, 509. SYNTHESIS A REVIEW.a
  168501. GABRIEL WEATHERHEAD
  168502. 10285
  168503. 11294N
  168504. 2/28/96VUM. SAINSBURY, SYNTHESIS OF 6H PYRIDO[4,3 B]CARBAZOLES, 1977, 437. SYNTHESIS A REVIEW.a
  168505. GABRIEL WEATHERHEAD
  168506. 10286
  168507. 11295N
  168508. 2/28/96V
  168509. B. T. BROBEL AND D. SEEBACH, POLARIZATION REVERSAL IN REACTIVITY OF CARBONYL COMPOUNDS VIA SULFUR CONTAINING REAGENTS, 1977, 357. SYNTHESIS A REVIEW.a
  168510. GABRIEL WEATHERHEAD
  168511. 10287
  168512. 11296N
  168513. 2/28/96VeS. RANGANATHAN, D. RANGANATHAN, AND A. K. MEHROTRA KETENE EQUIVALENTS, 1977, 289. SYNTHESIS A REVIEW.a
  168514. GABRIEL WEATHERHEAD
  168515. 10288
  168516. 11297N
  168517. 2/28/96
  168518. VbH. SUZUKI, SIDE REACTIONS IN AROMATIC NITRATION, SYNTHETIC ASPECTS, 1977, 217. SYNTHESIS A REVIEW.a
  168519. GABRIEL WEATHERHEAD
  168520. 10289
  168521. 11298N
  168522. 2/28/96VvS. M. ALI, T. V. LEE, AND S. M. ROBERT, BICYCLO[3.2.0]HEPTANONES AS VERSATILE. SYNTHONS, 1977,155. SYNTHESIS A REVIEW.a
  168523. GABRIEL WEATHERHEAD
  168524. 10290
  168525. 11299N
  168526. 2/28/96V
  168527. R. K. FRIEDLINA AND F. K. VELICHKO, SYNTHETIC APPLICATIONS OF HOMOLYTIC ADDITIONS AND TELOMERIZATION OF BROMINE CONTAINING ADDENDS, 1977,145. SYNTHESIS A REVIEW.a
  168528. GABRIEL WEATHERHEAD
  168529. 10291
  168530. 11300N
  168531. 2/28/96VrJ. K. RASMUSSEN, O SILYLATED ENOLATES
  168532. VERSATILE INTERMEDIATES FOR ORGANIC SYNTHESIS, 1977, 91. SYNTHESIS A REVIEW.a
  168533. GABRIEL WEATHERHEAD
  168534. 10292
  168535. 11301N
  168536. 2/28/96V
  168537. W. KANTLEHNER, B. FUNKE, E. HAUG, P. SPEH, L. KIENITZ AND T. MAIER, PREPARATIVE CHEMISTRY OF O  AND N FUNCTIONAL ORTHO CARBONIC ACID DERIVATIVES (IN GERMAN), 1977, 73. SYNTHESIS A REVIEW.a
  168538. GABRIEL WEATHERHEAD
  168539. 10293
  168540. 11302N
  168541. 2/28/96
  168542. C. BLOMBERG AND F. A. HARTOG, BARBIER REACTION
  168543.  ONE STEP ALTERNATIVE FOR SYNTHESES UIA ORGANOMAGNESIUM COMPOUNDS, 1977, 18. SYNTHESIS A REVIEW.a
  168544. GABRIEL WEATHERHEAD
  168545. 10294
  168546. 11303N
  168547. 2/28/96V
  168548. Y. TAMURA, J. MINAMIKAWA, AND M. IKEDA, O MESITYLENESULFONYLHYDROXYLAMINE AND RELATED POWERFUL AMINATING REAGENTS, 1977, 1. SYNTHESIS A REVIEW.a
  168549. GABRIEL WEATHERHEAD
  168550. 10295
  168551. 11304N
  168552. 2/28/96V
  168553. E. I. LEVKOEVA AND L. N. YAKHONTOV, SYNTHESIS OF HETEROCYCLIC ANALOGS OF PROSTAGLANDINS, 46, 565 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168554. GABRIEL WEATHERHEAD
  168555. 10296
  168556. 11305N
  168557. 2/28/96V
  168558. L. RASTEIKIENE, D. GREICIUTE, M. G. LIN'KOVA, AND I. L. KNUNYANTS, ADDITION OF SULFENYL CHLORIDES TO UNSATURATED COMPOUNDS, 46, 548 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168559. GABRIEL WEATHERHEAD
  168560. 10297
  168561. 11306N
  168562. 2/28/96V}V. B. MOCHALIN AND Y. N. PORSCHNEV, ADVANCES IN THE CHEMISTRY OF AZULENE, 46, 530 ( 1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.
  168563. GABRIEL WEATHERHEAD
  168564. 10298
  168565. 11307N
  168566. 2/28/96V
  168567. N. I. SHVETSOV SHILOVSKII, R. G. BOBKOVA, N. P. IGNATOVA AND N. N. MELNIKOV, COMPOUNDS OF TWO COORDINATE PHOSPHORUS, 46, 514 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168568. GABRIEL WEATHERHEAD
  168569. 10299
  168570. 11308N
  168571. 2/28/96V
  168572. V. KAMPARS AND O. NEILANDS ELECTRON AFFINITIES OF ORGANIC ELECTRON ACCEPTORS, 46, 945 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168573. GABRIEL WEATHERHEAD
  168574. 10300
  168575. 11309N
  168576. 2/28/96VpZ. V. ZVONKOVA, STRUCTURAL CHEMISTRY OF SUBSTITUTED BENZENES, 46, 479 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168577. GABRIEL WEATHERHEAD
  168578. 10301
  168579. 11310N
  168580. 2/28/96VsYU. V. MITIN AND N. P. ZAPELEVOVA, METHODS OF PEPTIDE SYNTHESIS, 46, 449 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168581. GABRIEL WEATHERHEAD
  168582. 10302
  168583. 11311N
  168584. 2/28/96V
  168585. V. T. OREKHOV, REACTIONS OF ORGANIC COMPOUNDS WITH HIGHER FLUORIDES OF GROUP V AND VI ELEMENTS, 46, 420 RUSSIAN CHEMICAL REVIEWS A REVIEW.
  168586. GABRIEL WEATHERHEAD
  168587. 10303
  168588. 11312N
  168589. 2/28/96VlA. N. VOLKOV AND A. N. NIKOL'SKAYA, ALPHA CYANOACETYLENES 46, 374 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168590. GABRIEL WEATHERHEAD
  168591. 10304
  168592. 11313N
  168593. 2/28/96V
  168594. V. G. GRANIK, A. M. ZHIDKOVA AND R. G. GLUSHKOV, ACETALS OF AMIDES AND LACTAMS, 46 361(1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168595. GABRIEL WEATHERHEAD
  168596. 10305
  168597. 11314N
  168598. 2/28/96VtL. S. KOBRINA, RADICAL REACTIONS OF AROMATIC POLYFLUOROCOMPOUNDS, 46, 348 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168599. GABRIEL WEATHERHEAD
  168600. 10306
  168601. 11315N
  168602. 2/28/96VXV. K. POGORELYI, WEAK HYDROGEN BONDS, 46, 316 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168603. GABRIEL WEATHERHEAD
  168604. 10307
  168605. 11316N
  168606. 2/28/96V]E. LUKEVICS, THE HYDROSILYLATION REACTION, 46, 264 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168607. GABRIEL WEATHERHEAD
  168608. 10308
  168609. 11317N
  168610. 2/28/96
  168611. E. M. CHERKASOVA, S. V. BOGATKOV, AND Z. P. GOLOVINA, TERTIARY AMINES IN ACYL TRANSFER REACTIONS, 46, 246 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168612. GABRIEL WEATHERHEAD
  168613. 10309
  168614. 11318N
  168615. 2/28/96V
  168616. V. D. ERMAKOVA, V. D. ARSENOR, M. I. CHERKASHIN, AND P. O. KISILITSA, PHOTOCHROMIC POLYMERS, 46,145 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168617. GABRIEL WEATHERHEAD
  168618. 10310
  168619. 11319N
  168620. 2/28/96VbV. KARNOJITZKY, AUTOOXIDATION OF AZO COMPOUNDS, 46, 121 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168621. GABRIEL WEATHERHEAD
  168622. 10311
  168623. 11320N
  168624. 2/28/96V
  168625. A. V. IVASHCHENKO AND V. M. DZIOMKO, REACTIONS OF ISATINS WITH AROMATIC AND HETEROCYCLIC ORTHO DIAMINES, 46, 115 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168626. GABRIEL WEATHERHEAD
  168627. 10312
  168628. 11321N
  168629. 2/28/96V
  168630. A. V. EL'TSOV, O. P. STUDZINSKII, AND V. M. GREBENKINA, PHOTOINITIATION OF THE REACTIONS OF QUINONES, 46, 93 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168631. GABRIEL WEATHERHEAD
  168632. 10313
  168633. 11322N
  168634. 2/28/96VtE. S. KRONGAUZ, MONO AND BIS ALPHA DIKETONES AND RELATED POLYMERS, 46, 59 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168635. GABRIEL WEATHERHEAD
  168636. 10314
  168637. 11323N
  168638. 2/28/96V
  168639. R. A. KHMEL'NITSKII AND YU. A. EFREMOV, REARRANGEMENTS IN SULFOXIDES AND SULFONES INDUCED BY ELECTRON IMPACT, 46, 46 (1977). RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  168640. GABRIEL WEATHERHEAD
  168641. 10315
  168642. 11324N
  168643. 2/28/96V
  168644. E. HECKER, NEW TOXIC, IRRITANT AND COCARCINOGENIC DITERPENE ESTERS FROM EUPHORBIACAE AND FROM THYMELAEACEAE, 49,1423 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168645. GABRIEL WEATHERHEAD
  168646. 10316
  168647. 11325N
  168648. 2/28/96VgJ. B. HARBORNE, CHEMOSYSTEMATICS AND COEVOLUTION, 49, 1403 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168649. GABRIEL WEATHERHEAD
  168650. 10317
  168651. 11326N
  168652. 2/28/96V
  168653. D. M. DODDRELL, STRUCTURAL APPLICATIONS OF NUCLEAR SPIN LATTICE RELAXATION TIMES, 49,1385 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168654. GABRIEL WEATHERHEAD
  168655. 10318
  168656. 11327N
  168657. 2/28/96VlK. L. RINEHART, JR., MUTASYNTHESIS OF NEW ANTIBIOTICS, 49, 1361 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168658. GABRIEL WEATHERHEAD
  168659. 10319
  168660. 11328N
  168661. 2/28/96VkR. DESLONGCHAMPS, SYNTHETIC STUDIES TOWARDS RYANODINE, 49,1329 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168662. GABRIEL WEATHERHEAD
  168663. 10320
  168664. 11329N
  168665. 2/28/96V
  168666. H. D. NIALL, MICROSEQUENCE ANALYSIS OF BIOLOGICALLY ACTIVE PROTEINS AND PEPTIDES, 49, 1323 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168667. GABRIEL WEATHERHEAD
  168668. 10321
  168669. 11330N
  168670. 2/28/96V
  168671. H. O. HUISMAN, SYNTHESES OF FUNCTIONALIZED ISOPRENE BUILDING BLOCKS AND THEIR APPLICATION TO DI  AND POLY ISOPRENOID SYNTHESES, 49,1307 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168672. GABRIEL WEATHERHEAD
  168673. 10322
  168674. 11331N
  168675. 2/28/96V
  168676. I. L. KARLE, MOLECULAR FORMULA, CONFIGURATION AND CONFORMATION BY X RAY ANALYSIS, 49,1291(1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168677. GABRIEL WEATHERHEAD
  168678. 10323
  168679. 11332N
  168680. 2/28/96
  168681. VkJ. MEINWALD, AN APPROACH TO THE SYNTHESIS OF PEDERIN, 49, 1275 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168682. GABRIEL WEATHERHEAD
  168683. 10324
  168684. 11333N
  168685. 2/28/96V
  168686. A. R. BATTERSBY, RECENT RESEARCHES ON THE BIOSYNTHESIS OF NATURAL PRODUCTS, 49,1251(1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168687. GABRIEL WEATHERHEAD
  168688. 10325
  168689. 11334N
  168690. 2/28/96V|D.H. R. BARTON, SYNTHESIS OF SPECIFICALLY FLUORINATED NATURAL PRODUCTS, 49,1241 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168691. GABRIEL WEATHERHEAD
  168692. 10326
  168693. 11335N
  168694. 2/28/96V
  168695. S. HANESSIAN AND G. RANCOURT, APPROACHES TO THE TOTAL SYNTHESIS OF NATURAL PRODUCTS FROM CARBOHYDRATES, 49, 1201 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168696. GABRIEL WEATHERHEAD
  168697. 10327
  168698. 11336N
  168699. 2/28/96VyL. SZABO, STRUCTURAL FEATURES OF THE BORDETELLA PERTUSSIS ENDOTOXIN, 49,1187 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168700. GABRIEL WEATHERHEAD
  168701. 10328
  168702. 11337N
  168703. 2/28/96
  168704. V}H. PAULSEN, SYNTHESIS OF AMINO  AND BRANCHED MONO  AND OLIGOSACCHARIDES, 49,1169 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168705. GABRIEL WEATHERHEAD
  168706. 10329
  168707. 11338N
  168708. 2/28/96VhB. COXON, NITROGEN 15 NMR STUDIES OF AMINO SUGARS, 49, 1151 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168709. GABRIEL WEATHERHEAD
  168710. 10330
  168711. 11339N
  168712. 2/28/96V~E. D. T. ATKINS, CONFORMATIONS OF URONIC ACID CONTAINING POLYSACCHARIDES, 49,1135 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168713. GABRIEL WEATHERHEAD
  168714. 10331
  168715. 11340N
  168716. 2/28/96VwG. O. ASPINAL, THE SELECTIVE DEGRADATION OF CARBOHYDRATE POLYMERS, 49,1105 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168717. GABRIEL WEATHERHEAD
  168718. 10332
  168719. 11341N
  168720. 2/28/96VvB. LINDBERG, STRUCTURAL STUDIES OF SOME BACTERIAL POLYSACCHARIDES 49,1085 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168721. GABRIEL WEATHERHEAD
  168722. 10333
  168723. 11342N
  168724. 2/28/96
  168725. L. HOUGH AND A. C. RICHARDSON, RECENT ASPECTS OF THE CHEMISTRY OF DISACCHARIDES 49,1069 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168726. GABRIEL WEATHERHEAD
  168727. 10334
  168728. 11343N
  168729. 2/28/96VkF. H. WESTHEIMER, THE HYDROLYSIS OF PHOSPHATE ESTERS, 49, 1059 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168730. GABRIEL WEATHERHEAD
  168731. 10335
  168732. 11344N
  168733. 2/28/96VyA. RASSAT, STEREOCHEMISTRY OF DISSOLVING METAL REDUCTION OF KETONES, 49,1049 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168734. GABRIEL WEATHERHEAD
  168735. 10336
  168736. 11345N
  168737. 2/28/96V
  168738. J. E. DUBOIS, STRAIN ENERGY MODELING OF SIMPLE AND CROWDED ALIPHATIC KETONES: SPECTROSCOPIC PROPERTIES, 49, 1029 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168739. GABRIEL WEATHERHEAD
  168740. 10337
  168741. 11346N
  168742. 2/28/96V
  168743. W. P. JENCKS AND H. F. GILBERT, GENERAL ACID BASE CATALYSIS OF CARBONYL AND ACYL GROUP REACTIONS, 49, 1021 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168744. GABRIEL WEATHERHEAD
  168745. 10338
  168746. 11347N
  168747. 2/28/96
  168748. VwE. K. EURANTO, MECHANISMS AND CATALYSIS IN VINYL ESTER HYDROLYSIS, 49,1009 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168749. GABRIEL WEATHERHEAD
  168750. 10339
  168751. 11348N
  168752. 2/28/96V
  168753. B. CAPON, MECHANISTIC STUDIES ON THE HYDROLYSIS OF ACETALS AND HEMIACETALS, 49,1001(1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168754. GABRIEL WEATHERHEAD
  168755. 10340
  168756. 11349N
  168757. 2/28/96V
  168758. W. KUTZELNIGG, QUANTUM CHEMICAL STUDIES OF CO, CS AND RELATED DOUBLE BONDS, 49, 981(1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168759. GABRIEL WEATHERHEAD
  168760. 10341
  168761. 11350N
  168762. 2/28/96VeC. A. BUNTON, MICELLAR CATALYSIS AND INHIBITION, 49, 969 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168763. GABRIEL WEATHERHEAD
  168764. 10342
  168765. 11351N
  168766. 2/28/96VkF. G. BORDWELL, EQUILIBRIUM ACIDITIES OF CARBON ACIDS, 49, 963 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168767. GABRIEL WEATHERHEAD
  168768. 10343
  168769. 11352N
  168770. 2/28/96
  168771. H. E. ZIMMERMAN, RECENT MECHANISTIC AND EXPLORATORY ORGANIC PHOTOCHEMISTRY, 49, 389 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168772. GABRIEL WEATHERHEAD
  168773. 10344
  168774. 11353N
  168775. 2/28/96V
  168776. D. G. WHITTEN, F. R. HOPF, F. H. QUINA, G. SPRINTSCHNIK, AND H. W. SPRINTSCHNIK, PHOTOCHEMISTRY OF ORGANIC CHROMOPHORES INCORPORATED INTO FATTY ACID MONOLAYERS, 49, 379 (1977) PURE AND APPLIED CHEMISTRY A REVIEW.a
  168777. GABRIEL WEATHERHEAD
  168778. 10345
  168779. 11354N
  168780. 2/28/96VoH. D. HARTZLER, AROMATIC ALDEHYDE LEUCO DYE PHOTOXIDATION, 49, 353 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168781. GABRIEL WEATHERHEAD
  168782. 10346
  168783. 11355N
  168784. 2/28/96V
  168785. T. ROSENFELD, B. HONIG, M. OTTOLENGHI, J. HURLEY, AND T. G. EBREY, CIS TRANS ISOMERIZATION IN THE PHOTOCHEMISTRY OF VISION, 49, 341(1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168786. GABRIEL WEATHERHEAD
  168787. 10347
  168788. 11356N
  168789. 2/28/96VlK. NAKANISHI, PHOTOCHEMICAL STUDIES OF VISUAL PIGMENTS, 49, 333 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.
  168790. GABRIEL WEATHERHEAD
  168791. 10348
  168792. 11357N
  168793. 2/28/96VxP. COURTOT, R. RUMIN, AND J. Y. SALAUN, PHOTOCHEMISTRY OF POLYENES, 49, 317 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168794. GABRIEL WEATHERHEAD
  168795. 10349
  168796. 11358N
  168797. 2/28/96V
  168798. J. STREITH, THE PHOTOCHEMISTRY OF AROMATIC N YLIDES. REARRANGEMENT AND FRAGMENTATION PATTERNS, 49, 305 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168799. GABRIEL WEATHERHEAD
  168800. 10350
  168801. 11359N
  168802. 2/28/96V
  168803. T. MUKAI, T. KUMAGAI, AND O. SESHIMOTO, PHOTOCHEMICAL AND THERMAL REACTIONS OF HETEROCYCLES CONTAINING C=N
  168804. O OR N=C
  168805. O GROUP, 49, 287 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168806. GABRIEL WEATHERHEAD
  168807. 10351
  168808. 11360N
  168809. 2/28/96V
  168810. P. J. WAGNER, EFFECTS OF METHYL SUBSTITUTION ON RATES OF TRIPLET STATE HYDROGEN ABSTRACTION BY THE BENZOYL GROUP, 49, 259 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168811. GABRIEL WEATHERHEAD
  168812. 10352
  168813. 11361N
  168814. 2/28/96
  168815. J. E. GUIILET, ENERGY TRANSFER AND MOLECULAR MOBILITY IN POLYMER PHOTOCHEMISTRY, 49, 249 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168816. GABRIEL WEATHERHEAD
  168817. 10353
  168818. 11362N
  168819. 2/28/96V
  168820. F. C. DE SCHRYVER, N. BOENS, J. HUYBRECHTS, J. DAEMEN, AND M. DE BRACKELAIRE, PHOTOCHEMISTRY OF BICHROMOPHORIC COMPOUNDS 49, 237 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168821. GABRIEL WEATHERHEAD
  168822. 10354
  168823. 11363N
  168824. 2/28/96VkN. C. BAIRD, AB INITIO CALCULATIONS IN PHOTOCHEMISTRY, 49, 223 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168825. GABRIEL WEATHERHEAD
  168826. 10355
  168827. 11364N
  168828. 2/28/96VLM. BENN, GLUCOSINOLATES, 49,197 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168829. GABRIEL WEATHERHEAD
  168830. 10356
  168831. 11365N
  168832. 2/28/96VxA. MARQUET, NEW ASPECTS OF THE CHEMISTRY OF BIOTIN AND SOME ANALOGS, 49,183 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168833. GABRIEL WEATHERHEAD
  168834. 10357
  168835. 11366N
  168836. 2/28/96
  168837. VsR. T. LALONDE AND C. WONG, SULFUR CONTAINING NUPHAR ALKALOIDS, 49, 169 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168838. GABRIEL WEATHERHEAD
  168839. 10358
  168840. 11367N
  168841. 2/28/96V
  168842. U. SCHMIDT, SYNTHESES AND INTERCONVERSIONS OF ALPHA MERCAPTO ALPHA AMINO ACIDS AND DEHYDRO AMINO ACIDS, 49,163 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168843. GABRIEL WEATHERHEAD
  168844. 10359
  168845. 11368N
  168846. 2/28/96V
  168847. S. OAE, Y. H. KIM, D. FUKUSHIMA, AND T. TAKATA, OXIDATION OF BIOLOGICALLY ACTIVE AND RELATED SULFUR CONTAINING COMPOUNDS, 49,153 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168848. GABRIEL WEATHERHEAD
  168849. 10360
  168850. 11369N
  168851. 2/28/96VzA. KJAER, LOW MOLECULAR WEIGHT SULPHUR CONTAINING COMPOUNDS IN NATURE, 49,137 (1977). PURE AND APPLIED CHEMISTRY A REVIEW.a
  168852. GABRIEL WEATHERHEAD
  168853. 10361
  168854. 11370N
  168855. 2/28/96V
  168856. G. L. NELSON AND E. A. WILLIAMS, ELECTRONIC STRUCTURE AND 13C NMR, 12, 229 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168857. GABRIEL WEATHERHEAD
  168858. 10362
  168859. 11371N
  168860. 2/28/96VwJ. L. JENSEN, HEATS OF HYDROGENATION: A BRIEF SUMMARY, 12, 189 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168861. GABRIEL WEATHERHEAD
  168862. 10363
  168863. 11372N
  168864. 2/28/96
  168865.  W. J. HEHRE, R. W. TAFT, AND R. D. TOPSOM, AB INITIO CALCULATIONS OF CHARGE DISTRIBUTIONS IN MONOSUBSTITUTED BENZENES AND IN META  AND PARA SUBSTITUTED FLUOROBENZENES. COMPARISON WITH LH, 13C, AND L9F NMR SUBSTITUENT SHIFTS, 12,159 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.
  168866. GABRIEL WEATHERHEAD
  168867. 10364
  168868. 11373N
  168869. 2/28/96V
  168870. L. S. LEVITT AND H. F. WIDING, THE ALKYL INDUCTIVE EFFECT. CALCULATION OF INDUCTIVE SUBSTITUENT PARAMETERS, 12, 119 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168871. GABRIEL WEATHERHEAD
  168872. 10365
  168873. 11374N
  168874. 2/28/96V
  168875. S. H. UNGER AND C. HANSCH, QUANTITATIVE MODELS OF STERIC EFFECTS, 12, 91(1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168876. GABRIEL WEATHERHEAD
  168877. 10366
  168878. 11375N
  168879. 2/28/96
  168880. V|T. FUJITA AND T. NISHIOKA, THE ANALYSIS OF THE ORTHO EFFECT, 12, 49 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168881. GABRIEL WEATHERHEAD
  168882. 10367
  168883. 11376N
  168884. 2/28/96VxL. M. STOCK, A CLASSIC MECHANISM FOR AROMATIC NITRATION, 12, 21 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168885. GABRIEL WEATHERHEAD
  168886. 10368
  168887. 11377N
  168888. 2/28/96V
  168889. R. D. TOPSOM, THE NATURE AND ANALYSIS OF SUBSTITUENT ELECTRONIC EFFECTS, 12,1 (1976). PROGRESS IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  168890. GABRIEL WEATHERHEAD
  168891. 10369
  168892. 11378N
  168893. 2/28/96V
  168894. H. H. MANTSCH, H. SAITO AND I. C. P. SMITH, DEUTERIUM MAGNETIC RESONANCE, 11, 211(1977). PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  168895. GABRIEL WEATHERHEAD
  168896. 10370
  168897. 11379N
  168898. 2/28/96VyV. S. PETROSYAN, NMR SPECTRA AND STRUCTURES OF ORGANOTIN COMPOUNDS, 11,115 (1977). PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  168899. GABRIEL WEATHERHEAD
  168900. 10371
  168901. 11380N
  168902. 2/28/96
  168903. VaB. E. MANN, DYNAMIC 13C NMR SPECTROSCOPY, 11, 95 ( 1977) . PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  168904. GABRIEL WEATHERHEAD
  168905. 10372
  168906. 11381N
  168907. 2/28/96VjJ. N. SHOOLERY, QUANTITATIVE APPLICATIONS OF 13C NMR, 11, 79 (1977) PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  168908. GABRIEL WEATHERHEAD
  168909. 10373
  168910. 11382N
  168911. 2/28/96V
  168912. P. HEMMERICH, FLAVIN AND FLAVOCOENZYME CHEMISTRY, 33, 451 (1976). PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  168913. GABRIEL WEATHERHEAD
  168914. 10374
  168915. 11383N
  168916. 2/28/96V
  168917. A. FONTANA AND C. TONIOLO, CHEMISTRY OF TRYPTOPHANE IN PEPTIDES AND PROTEINS 33, 309 (1976). PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  168918. GABRIEL WEATHERHEAD
  168919. 10375
  168920. 11384N
  168921. 2/28/96V
  168922. K. L. RINEHART AND L. S. SHIELD, CHEMISTRY OF THE ANSAMYCIN ANTIBIOTICS, 33, 231(1976). PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  168923. GABRIEL WEATHERHEAD
  168924. 10376
  168925. 11385N
  168926. 2/28/96
  168927. R. M. COATES, BIOGENETIC TYPE REARRANGEMENTS OF TERPENES, 33, 73 (1976). PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  168928. GABRIEL WEATHERHEAD
  168929. 10377
  168930. 11386N
  168931. 2/28/96V
  168932. I,. MINALE, G. CIMINO, S. DE STEFANO, AND G. SODANO, NATURAL PRODUCTS FROM PORIFERA, 33,1(1976). PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  168933. GABRIEL WEATHERHEAD
  168934. 10378
  168935. 11387N
  168936. 2/28/96VSN. RABJOHN, SELENIUM DIOXIDE OXIDATION, 24, 421 (1976). ORGANIC REACTIONS A REVIEW.a
  168937. GABRIEL WEATHERHEAD
  168938. 10379
  168939. 11388N
  168940. 2/28/96V
  168941. C. S. RONDESVEDT, ARYLATION OF UNSATURATED COMPOUNDS BY DIAZONIUM SALTS (MEERWEIN ARYLATION), 24, 225 (1976) . ORGANIC REACTIONS A REVIEW.a
  168942. GABRIEL WEATHERHEAD
  168943. 10380
  168944. 11389N
  168945. 2/28/96V_J. E. MCMURRY, ESTER CLEAVAGE VIA SN2 DEALKYLATION, 24, 187 (1976). ORGANIC REACTIONS A REVIEW.a
  168946. GABRIEL WEATHERHEAD
  168947. 10381
  168948. 11390N
  168949. 2/28/96
  168950. A. J. BIRCH AND D. H. WILLIAMSON, HOMOGENEOUS HYDROGENATION CATALYSTS IN ORGANIC SYNTHESIS, 24,1(1976). ORGANIC REACTIONS A REVIEW.a
  168951. GABRIEL WEATHERHEAD
  168952. 10382
  168953. 11391N
  168954. 2/28/96V
  168955. J. P. KUTNEY, STUDIES IN INDOLE ALKALOID SYNTHESIS. A GENERAL SYNTHETIC ROUTE TO 2 ACYLINDOLE ALKALOIDS AND RELATED COMPOUNDS, 8, 813 (1977). HETEROCYCLES A REVIEW.a
  168956. GABRIEL WEATHERHEAD
  168957. 10383
  168958. 11392N
  168959. 2/28/96V
  168960. I. KITAGAWA AND M. YOSHIKAWA, SELECTIVE CLEAVAGE OF GLUCURONIDE LINKAGE IN OLIGOGLYCOSIDES, 8, 783 (1977). HETEROCYCLES A REVIEW.a
  168961. GABRIEL WEATHERHEAD
  168962. 10384
  168963. 11393N
  168964. 2/28/96VhT. HINO AND M. NAKAGAWA, OXIDATION OF INDOLES WITH TRIPLET OXYGEN, 8, 743 (1977). HETEROCYCLES A REVIEW.a
  168965. GABRIEL WEATHERHEAD
  168966. 10385
  168967. 11394N
  168968. 2/28/96V
  168969. T. HIRAOKA, Y. SUGIMURA, T. SAITO, AND T. KOBAYASHI RECENT ADVANCES IN THE SYNTHESIS OF 7 METHOXYCEPHALOSPORINS (CEPHAMYCINS), 8, 719 (1977). HETEROCYCLES A REVIEW.a
  168970. GABRIEL WEATHERHEAD
  168971. 10386
  168972. 11395N
  168973. 2/28/96V
  168974. R. TACHIKAWA, A. TERADA, K. TOMITA, AND T. IWAOKA SYNTHESIS AND REACTION OF 2 ALLYLINDOLES, 8, 695 (1977). HETEROCYCLES A REVIEW.a
  168975. GABRIEL WEATHERHEAD
  168976. 10387
  168977. 11396N
  168978. 2/28/96V
  168979. T. KUNIEDA AND T. TAKIZAWA, FREE RADICAL TELOMERIZATION OF VINYLENE CARBONATE (1,3 DIOXOL 2 ONE) WITH POLYHALOMETHANES
  168980. CHEMISTRY AND SYNTHETIC APPLICATIONS OF TELOMERS, 8, 661(1977). HETEROCYCLES A REVIEW.a
  168981. GABRIEL WEATHERHEAD
  168982. 10388
  168983. 11397N
  168984. 2/28/96V
  168985. Y. INUBUSHI AND T. IBUAK, SYNTHESIS OF PUMILIOTOXIN C. A TOXIC ALKALOID FROM CENTRAL AMERICAN ARROW POISON FROG, DENDROBATES PUMILIO AND D. AURATUS, 8, 633 (1977). HETEROCYCLES A REVIEW.a
  168986. GABRIEL WEATHERHEAD
  168987. 10389
  168988. 11398N
  168989. 2/28/96V
  168990. U. K. PANDIT, REACTION OF CARBENES WITH PYRIMIDINES AND ISOQUINOLINE DERIVATIVES. APPROACHES TO THE SYNTHESIS OF MODIFIED NUCLEOSIDES AND ALKALOIDS, 8, 609 (1977). HETEROCYCLES A REVIEW.a
  168991. GABRIEL WEATHERHEAD
  168992. 10390
  168993. 11399N
  168994. 2/28/96
  168995. ViS. NAKAMURA AND H. KONDO, A BRIEF REVIEW OF NUCLEOSIDE ANTIBIOTICS, 8, 583 (1977). HETEROCYCLES A REVIEW.a
  168996. GABRIEL WEATHERHEAD
  168997. 10391
  168998. 11400N
  168999. 2/28/96V
  169000. Y. ASAKAWA AND T. TAKEMOTO, SESQUITERPENE LACTONES AND HETEROCYCLIC COMPOUNDS OF BRYOPHYTA, 8, 563 (1977). HETEROCYCLES A REVIEW.a
  169001. GABRIEL WEATHERHEAD
  169002. 10392
  169003. 11401N
  169004. 2/28/96VzT. KAMETANI AND K. FUKUMOTO, NEW METHODS IN THE TOTAL SYNTHESES OF NATURAL PRODUCTS, 8, 465 (1977). HETEROCYCLES A REVIEW.a
  169005. GABRIEL WEATHERHEAD
  169006. 10393
  169007. 11402N
  169008. 2/28/96VWE. FUJITA AND M. NODE, SYNTHESIS OF GIBBERELLINS, 7, 709 (1977). HETEROCYCLES A REVIEW.a
  169009. GABRIEL WEATHERHEAD
  169010. 10394
  169011. 11403N
  169012. 2/28/96V~W. A. AYER AND L. M. BROWNE, THE LADYBUG ALKALOIDS INCLUDING SYNTHESIS AND BIOSYNTHESIS, 7, 685 (1977). HETEROCYCLES A REVIEW.a
  169013. GABRIEL WEATHERHEAD
  169014. 10395
  169015. 11404N
  169016. 2/28/96
  169017. VpT. R. GOVINDACHARI AND P. C. PARTHASARATHY, ALKALOIDS OF ANCISTROCLADACEAE, 7, 661(1977). HETEROCYCLES A REVIEW.a
  169018. GABRIEL WEATHERHEAD
  169019. 10396
  169020. 11405N
  169021. 2/28/96V
  169022. R. BONNETT AND P. NICOLAIDOU, NITRITE AND THE ENVIRONMENT. THE NITROSATION OF O AMINO ACID DERIVATIVES, 7, 637 (1977). HETEROCYCLES A REVIEW.a
  169023. GABRIEL WEATHERHEAD
  169024. 10397
  169025. 11406N
  169026. 2/28/96V
  169027. T. KAMETANI AND K. FUKUMOTO, SYNTHESES OL QUINAZOLONE ALKALOIDS AND BENZOXAZINONES BY RETRO MASS SPECTRAL SYNTHESIS AND RELATED ANALYSIS, 7, 615 (1977). HETEROCYCLES A REVIEW.a
  169028. GABRIEL WEATHERHEAD
  169029. 10398
  169030. 11407N
  169031. 2/28/96VcJ. P. KUTNEY, DIHYDROPYRIDINES IN BIOSYNTHESIS AND SYNTHESIS, 7, 593 (1977). HETEROCYCLES A REVIEW.a
  169032. GABRIEL WEATHERHEAD
  169033. 10399
  169034. 11408N
  169035. 2/28/96VnA. V. KAMERNITZKY AND A. M. TURUTA, SYNTHESIS OF STEROIDAL HETEROCYCLES, 7, 547 (1977). HETEROCYCLES A REVIEW.a
  169036. GABRIEL WEATHERHEAD
  169037. 10400
  169038. 11409N
  169039. 2/28/96
  169040. S. RANGANATHAN AND C. S. PANDA, FASCINATING PROBLEMS IN ORGANIC REACTION MECHANISMS VIII: REACTIONS AND REARRANGEMENTS OF PHENANTHRAQUINONE MONOIMINE, 7, 529 (1977). HETEROCYCLES A REVIEW.a
  169041. GABRIEL WEATHERHEAD
  169042. 10401
  169043. 11410N
  169044. 2/28/96VrS. RAJAPPA, THE SYNTHESIS OF HETEROCYCLES FROM ENAMINES AND ISOTHIOCYANATES, 7, 507 (1977). HETEROCYCLES A REVIEW.a
  169045. GABRIEL WEATHERHEAD
  169046. 10402
  169047. 11411N
  169048. 2/28/96V
  169049. G. W. KRAMER AND H. C. BROWN, A REMARKABLE REARRANGEMENT OF LITHIUM DIALKYL 9 BORABICYCLO[3.3.1]NONANE ATE COMPLEXES, 7, 487 (1977). HETEROCYCLES A REVIEW.a
  169050. GABRIEL WEATHERHEAD
  169051. 10403
  169052. 11412N
  169053. 2/28/96V
  169054. H. C. BROWN AND C. F. LANE, 9 BORABICYCLO[3.3.1]NONANE. A MOST UNUSUAL HETEROCYCLIC DIALKYLBORANE, 7, 453 HETEROCYCLES A REVIEW.a
  169055. GABRIEL WEATHERHEAD
  169056. 10404
  169057. 11413N
  169058. 2/28/96V
  169059. K. GOLANKIEWICZ, SYNTHESIS AND SOME PHYSICAL AND PHOTOCHEMICAL PROPERTIES OF DINUCLEOTIDE ANALOGS, 7, 429 (1977). HETEROCYCLES A REVIEW.a
  169060. GABRIEL WEATHERHEAD
  169061. 10405
  169062. 11414N
  169063. 2/28/96V
  169064. C. O. OKAFOR, CHEMISTRY AND APPLICATIONS OF AZA  AND THIA ANALOGS OF PHENOXAZINE AND RELATED COMPOUNDS, 7, 391 (1977). HETEROCYCLES A REVIEW.a
  169065. GABRIEL WEATHERHEAD
  169066. 10406
  169067. 11415N
  169068. 2/28/96VVV. NAIR AND K. H. KIM, L AZIRINE RING CHEMISTRY, 7, 353 (1977). HETEROCYCLES A REVIEW.a
  169069. GABRIEL WEATHERHEAD
  169070. 10407
  169071. 11416N
  169072. 2/28/96V
  169073. J. STREITH, PHOTOCHEMISTRY IN HETEROCYCLIC SYNTHESIS. FROM PYRIDINIUM N YLIDES TO DIAZEPINES AND BEYOND, 6 2021 (1977). HETEROCYCLES A REVIEW.a
  169074. GABRIEL WEATHERHEAD
  169075. 10408
  169076. 11417N
  169077. 2/28/96VwM. A. KHAN AND J. F. DA ROCHA, PYRROLOQUINOLINES II. LH PYRROLO[3,2 B]QUINOLINES, 6 1927 (1977). HETEROCYCLES A REVIEW.a
  169078. GABRIEL WEATHERHEAD
  169079. 10409
  169080. 11418N
  169081. 2/28/96V
  169082. S. HIBINO, SYNTHETIC APPROACHES TO STREPTONIGRIN AND BIOLOGICAL ACTIVITIES OF THE QUINOLINEQUINONE SYSTEMS, 6 1485 (1977). HETEROCYCLES A REVIEW.a
  169083. GABRIEL WEATHERHEAD
  169084. 10410
  169085. 11419N
  169086. 2/28/96
  169087. V|S. F. DYKE, ISOQUINOLINE ALKALOID BIOSYNTHESIS. SPECULATIONS ON SOME UNSOLVED PROBLEMS, 6,1441(1977). HETEROCYCLES A REVIEW.a
  169088. GABRIEL WEATHERHEAD
  169089. 10411
  169090. 11420N
  169091. 2/28/96V
  169092. B. R. PAI, K. NAGARAJAN, H. SUGUNA, AND S. NATARAJAN, RECENT WORK ON PROTOBERBERINES AND TETRAHYDROPROTOBERBERINES, 6,1377 (1977). HETEROCYCLES A REVIEW.a
  169093. GABRIEL WEATHERHEAD
  169094. 10412
  169095. 11421N
  169096. 2/28/96VwM. A. KHAN AND J. F. DA ROCHA, PYRROLOQUINOLINES I. 1H PYRROLO[2,3 B]QUINOLINES, 6, 1229 (1977). HETEROCYCLES A REVIEW.a
  169097. GABRIEL WEATHERHEAD
  169098. 10413
  169099. 11422N
  169100. 2/28/96VrF. D. POPP AND R. F. WATTS, THE CHEMISTRY OF THE BENZO[A]QUINOLIZINE SYSTEM, 6 1189 (1977). HETEROCYCLES A REVIEW.a
  169101. GABRIEL WEATHERHEAD
  169102. 10414
  169103. 11423N
  169104. 2/28/96VjS. SKONIECZNY, SYNTHESIS OF THE 9 SUBSTITUTED ACRIDINES (1970 1976), 6, 987 (1977). HETEROCYCLES A REVIEW.a
  169105. GABRIEL WEATHERHEAD
  169106. 10415
  169107. 11424N
  169108. 2/28/96
  169109. C. KASHIMA, Y. YAMAMOTO, AND Y. TSUDA, THE REACTION OF 3,5 DIMETHYLISOXAZOLE WITH SOME ELECTROPHILES, 6, 805 (1977). HETEROCYCLES A REVIEW.a
  169110. GABRIEL WEATHERHEAD
  169111. 10416
  169112. 11425N
  169113. 2/28/96V
  169114. J. APSIMON AND A. HOLMES, APPLICATION OF HETEROCYCLES TO THE SYNTHESIS OF CARBONYL COMPOUNDS, 6, 731(1977). HETEROCYCLES A REVIEW.a
  169115. GABRIEL WEATHERHEAD
  169116. 10417
  169117. 11426N
  169118. 2/28/96V\S. OAE AND K. OGINO, REARRANGEMENTS OF T AMINE OXIDES, 6, 583 (1977). HETEROCYCLES A REVIEW.a
  169119. GABRIEL WEATHERHEAD
  169120. 10418
  169121. 11427N
  169122. 2/28/96VSW. DOPKE, LACTONALKALOIDE AUS AMARYLLIDACEEN, 6, 551 (1977). HETEROCYCLES A REVIEW.a
  169123. GABRIEL WEATHERHEAD
  169124. 10419
  169125. 11428N
  169126. 2/28/96V
  169127. V. SIMANEK AND V. PREININGER PSEUDOBASE FORMATION FROM QUATERNARY PYRIDINIUM, QUINOLINIUM AND ISOQUINOLINIUM CATIONS, 6, 475 (1977). HETEROCYCLES A REVIEW.a
  169128. GABRIEL WEATHERHEAD
  169129. 10420
  169130. 11429N
  169131. 2/28/96
  169132. P. GILGEN, H. HEIMGARTNER, H. SCHMID, AND H. J. HANSEN, A REVIEW ON THE PHOTOCHEMISTRY OF 2H AZIRINES, 6,143 (1977). HETEROCYCLES A REVIEW.a
  169133. GABRIEL WEATHERHEAD
  169134. 10421
  169135. 11430N
  169136. 2/28/96V
  169137. B. P. MUNDY, K. B. LIPKOWITZ, AND G. W. DIRKS, CHEMISTRY OF THE 6,8 DIOXABICYCLO[3.2.1]OCTANE SERIES. SOURCES, SYNTHESES, STRUCTURES AND REACTIONS, 6, 51(1977). HETEROCYCLES A REVIEW.a
  169138. GABRIEL WEATHERHEAD
  169139. 10422
  169140. 11431N
  169141. 2/28/96V
  169142. D. J. BURTON AND J. L. HAHNFELD, PREPARATION AND REACTIONS OF FLUOROMETHYLENES, 8,119 (1977). FLUORINE CHEMISTRY REVIEWS A REVIEW.a
  169143. GABRIEL WEATHERHEAD
  169144. 10423
  169145. 11432N
  169146. 2/28/96Vz0. PALETA, IONIC ADDITION REACTIONS OF HALOMETHANES WITH FLUOROOLEFINS, 8, 39 (1977). FLUORINE CHEMISTRY REVIEWS A REVIEW.a
  169147. GABRIEL WEATHERHEAD
  169148. 10424
  169149. 11433N
  169150. 2/28/96VoR. FILLER, THE PENTAFLUOROPHENYL GROUP; EFFECTS ON REACTIVITY, 8, 1(1977). FLUORINE CHEMISTRY REVIEWS A REVIEW.a
  169151. GABRIEL WEATHERHEAD
  169152. 10425
  169153. 11434
  169154. 2/28/96V~A. WILLIAMS AND K. T. DOUGLAS, ACYL GROUP TRANSFER ELIMINATION ADDITION MECHANISM, 1977, 679. CHEMISTRY AND INDUSTRY A REVIEW.a
  169155. GABRIEL WEATHERHEAD
  169156. 10426
  169157. 11435N
  169158. 2/28/96VfH. G. VIEHE, HETEROCYCLIZATIONS WITH NEW IMINIUM SYNTHONS, 1977, 386. CHEMISTRY AND INDUSTRY A REVIEW.a
  169159. GABRIEL WEATHERHEAD
  169160. 10427
  169161. 11436N
  169162. 2/28/96V^R. J. STOODLEY, ASPECTS OF HETEROCYCLIC SYNTHESIS, 1977, 377. CHEMISTRY AND INDUSTRY A REVIEW.a
  169163. GABRIEL WEATHERHEAD
  169164. 10428
  169165. 11437N
  169166. 2/28/96V
  169167. R. J. HAYWARD, M. HTAY, AND O. METH COHN, NOVEL HETEROCYCLES RELATED TO CROWN ETHERS, 1977, 373. CHEMISTRY AND INDUSTRY A REVIEW.a
  169168. GABRIEL WEATHERHEAD
  169169. 10429
  169170. 11438N
  169171. 2/28/96V|D. P. N. SATCHELL, METAL ION PROMOTED REACTIONS OF ORGANOSULFUR COMPOUNDS, 6, 345 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169172. GABRIEL WEATHERHEAD
  169173. 10430
  169174. 11439N
  169175. 2/28/96VNJ. V. GREENHILL, ENAMINONES, 6, 277 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.
  169176. GABRIEL WEATHERHEAD
  169177. 10431
  169178. 11440N
  169179. 2/28/96VcR. L. WAIN, CHEMICALS WHICH CONTROL PLANT GROWTH, 6, 261 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169180. GABRIEL WEATHERHEAD
  169181. 10432
  169182. 11441N
  169183. 2/28/96V^E. LEE RUFF, ORGANIC CHEMISTRY OF SUPEROXIDE, 6,195 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169184. GABRIEL WEATHERHEAD
  169185. 10433
  169186. 11442N
  169187. 2/28/96VnP. E. GEORGHIOU, CHEMISTRY OF VITAMIN D: HORMONE CALCIFEROLS, 6, 83 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169188. GABRIEL WEATHERHEAD
  169189. 10434
  169190. 11443N
  169191. 2/28/96VWA. C. PRATT, PHOTOCHEMISTRY OF IMINES, 6, 63 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169192. GABRIEL WEATHERHEAD
  169193. 10435
  169194. 11444N
  169195. 2/28/96V
  169196. T. K. BRADSHAW AND D. W. HUTCHINSON, 5 SUBSTITUTED PYRIMIDINE NUCLEOSIDES AND NUCLEOTIDES, 6, 43 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169197. GABRIEL WEATHERHEAD
  169198. 10436
  169199. 11445N
  169200. 2/28/96
  169201. 9V^G. W. KIRBY, ELECTROPHILIC C NITROSO COMPOUNDS, 6,1 (1977). CHEMICAL SOCIETY REVIEWS A REVIEW.a
  169202. GABRIEL WEATHERHEAD
  169203. 10437
  169204. 11446N
  169205. 2/28/96VTA. EFRATY, CYCLOBUTADIENEMETAL COMPLEXES, 77, 691 (1977). CHEMICAL REVIEWS A REVIEW.a
  169206. GABRIEL WEATHERHEAD
  169207. 10438
  169208. 11447N
  169209. 2/28/96V
  169210. A. R. KATRITZKY AND R. D. TOPSOM, INFRARED INTENSITIES: A GUIDE TO INTRAMOLECULAR INTERACTIONS IN CONJUGATED SYSTEMS, 77, 639 (1977). CHEMICAL REVIEWS A REVIEW.a
  169211. GABRIEL WEATHERHEAD
  169212. 10439
  169213. 11448N
  169214. 2/28/96V
  169215. H. GUNTHER AND G. JIKELI, NMR SPECTRA OF CYCLIC MONOENES: HYDROCARBONS, KETONES, HETEROCYCLES, AND BENZO DERIVATIVES, 77, 599 (1977). CHEMICAL REVIEWS A REVIEW.a
  169216. GABRIEL WEATHERHEAD
  169217. 10440
  169218. 11449N
  169219. 2/28/96V
  169220. G. R. NEWKOME, J. D. SAUER, J. M. ROPER, AND D. C. HAGER, CONSTRUCTION OF SYNTHETIC MACROCYCLIC COMPOUNDS POSSESSING SUBHETEROCYCLIC RINGS, SPECIFICALLY PYRIDINE, FURAN, AND THIOPHENE, 77, 513 (1977). CHEMICAL REVIEWS A REVIEW.
  169221. GABRIEL WEATHERHEAD
  169222. 10441
  169223. 11450N
  169224. 2/28/96V
  169225. S. BRASLAVSKY AND J. HEICKLEN, THE GAS PHASE THERMAL AND PHOTOCHEMICAL DECOMPOSITION OF HETEROCYCLIC COMPOUNDS CONTAINING NITROGEN, OXYGEN, OR SULFUR, 77, 473 (1977). CHEMICAL REVIEWS A REVIEW.a
  169226. GABRIEL WEATHERHEAD
  169227. 10442
  169228. 11451N
  169229. 2/28/96VfT. L. GILCHRIST AND C. J. MOODY, CHEMISTRY OF SULFILIMINES, 77, 409 (1977). CHEMICAL REVIEWS A REVIEW.a
  169230. GABRIEL WEATHERHEAD
  169231. 10443
  169232. 11452N
  169233. 2/28/96VeR. ENGEL, PHOSPHONATES AS ANALOGUES OF NATURAL PHOSPHATES, 77, 349 (1977). CHEMICAL REVIEWS A REVIEW.a
  169234. GABRIEL WEATHERHEAD
  169235. 10444
  169236. 11453N
  169237. 2/28/96V
  169238. C. A. TOLMAN, STERIC EFFECTS OF PHOSPHORUS LIGANDS IN ORGANOMETALLIC CHEMISTRY AND HOMOGENEOUS CATALYSIS, 77, 313 (1977). CHEMICAL REVIEWS A REVIEW.a
  169239. GABRIEL WEATHERHEAD
  169240. 10445
  169241. 11454N
  169242. 2/28/96V
  169243. I. SCHMELTZ AND D. HOFFMANN, NITROGEN CONTAINING COMPOUNDS IN TOBACCO AND TOBACCO SMOKE, 77, 295 (1977). CHEMICAL REVIEWS A REVIEW.
  169244. GABRIEL WEATHERHEAD
  169245. 10446
  169246. 11455N
  169247. 2/28/96VnV. AMARNATH AND A. D. BROOM, CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDES, 77,183 (1977). CHEMICAL REVIEWS A REVIEW.a
  169248. GABRIEL WEATHERHEAD
  169249. 10447
  169250. 11456N
  169251. 2/28/96V
  169252. S. D. VENKATARAMU, G. D. MACDONELL, W. R. PURDUM, M. EL DEEK, AND K. D. BERLIN POLYCYCLIC CARBON PHOSPHORUS HETEROCYCLES, 77,121 (1977). CHEMICAL REVIEWS A REVIEW.a
  169253. GABRIEL WEATHERHEAD
  169254. 10448
  169255. 11457N
  169256. 2/28/96VoR. D. HOWELLS AND J. D. MCCOWN, TRIFLUOROMETHANESULFONIC ACID AND DERIVATIVES, 77, 69 (1977). REVIEWS A REVIEW.a
  169257. GABRIEL WEATHERHEAD
  169258. 10449
  169259. 11458N
  169260. 2/28/96VeA. PADWA, PHOTOCHEMISTRY OF THE CARBON NITROGEN DOUBLE BOND 77, 37 (1977). CHEMICAL REVIEWS A REVIEW.a
  169261. GABRIEL WEATHERHEAD
  169262. 10450
  169263. 11459N
  169264. 2/28/96V
  169265. D. C. PALMER AND M. J. STRAUSS, BENZOMORPHANS: SYNTHESIS, STEREOCHEMISTRY REACTIONS, AND SPECTROSCOPIC CHARACTERIZATIONS, 77, 1 (1977). CHEMICAL REVIEWS A REVIEW.a
  169266. GABRIEL WEATHERHEAD
  169267. 10451
  169268. 11460N
  169269. 2/28/96V
  169270. H. MEIER AND K. P. ZELLER, THERMAL AND PHOTOCHEMICAL CYCLOELIMINATION OF NITROGEN, 16, 835 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169271. GABRIEL WEATHERHEAD
  169272. 10452
  169273. 11461N
  169274. 2/28/96V
  169275. T. SAEGUSA, SPONTANEOUS ALTERNATING COPOLYMERIZATION UIA ZWITTERIONS, 16, 826 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169276. GABRIEL WEATHERHEAD
  169277. 10453
  169278. 11462N
  169279. 2/28/96V
  169280. T. MUKAIYAMA, TITANIUM TETRACHLORIDE IN ORGANIC SYNTHESIS, 16, 817 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169281. GABRIEL WEATHERHEAD
  169282. 10454
  169283. 11463N
  169284. 2/28/96V
  169285. H. HAGEMANN, SYNTHESIS AND REACTIONS OF N CHLORO  CARBONYL ISOCYANATE, 16, 743 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169286. GABRIEL WEATHERHEAD
  169287. 10455
  169288. 11464N
  169289. 2/28/96
  169290. E. KUHLE AND E. KLAUKE, FLUORINATED ISOCYANATES AND DERIVATIVES AS INTERMEDIATES FOR BIOLOGICALLY ACTIVE COMPOUNDS, 16, 736 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169291. GABRIEL WEATHERHEAD
  169292. 10456
  169293. 11465N
  169294. 2/28/96VxH. ZAHNER, ASPECTS OF ANTIBIOTIC RESEARCH, 16, 687 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169295. GABRIEL WEATHERHEAD
  169296. 10457
  169297. 11466N
  169298. 2/28/96V
  169299. M. J. ARONEY, ELECTRO OPTICAL KERR EFFECT IN CONFORMATIONAL ANALYSIS, 16, 663 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169300. GABRIEL WEATHERHEAD
  169301. 10458
  169302. 11467N
  169303. 2/28/96V
  169304. H. BOCK, MOLECULAR STATES AND MOLECULAR ORBITALS, 16, 613 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169305. GABRIEL WEATHERHEAD
  169306. 10459
  169307. 11468N
  169308. 2/28/96
  169309. S. MASAMUNE, G. S. BATES, AND J. W. CORCORAN, MACROLIDE CHEMISTRY AND BIOCHEMISTRY, 16, 685 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169310. GABRIEL WEATHERHEAD
  169311. 10460
  169312. 11469N
  169313. 2/28/96V
  169314. R. HUISGEN, ELECTROCYCLIC RING OPENING REACTIONS OF ETHYLENE OXIDES, 16, 672 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169315. GABRIEL WEATHERHEAD
  169316. 10461
  169317. 11470N
  169318. 2/28/96V
  169319. J. H. PERLSTEIN, ORGANIC METALS, INTERMOLECULAR MIGRATION OF AROMATICITY, 16, 619 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169320. GABRIEL WEATHERHEAD
  169321. 10462
  169322. 11471N
  169323. 2/28/96V
  169324. E. V. DEHMLOW, ADVANCES IN PHASE TRANSFER CATALYSIS, 16, 493 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169325. GABRIEL WEATHERHEAD
  169326. 10463
  169327. 11472N
  169328. 2/28/96
  169329. H. FORSTER AND F. VOGTLE, STERIC INTERACTIONS IN ORGANIC CHEMISTRY, SPATIAL REQUIREMENTS OF SUBSTITUENTS, 16, 429 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169330. GABRIEL WEATHERHEAD
  169331. 10464
  169332. 11473N
  169333. 2/28/96V
  169334. H. POMMER, THE WITTIG REAETION IN INDUSTRIAL PRAETICE, 16, 423 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169335. GABRIEL WEATHERHEAD
  169336. 10465
  169337. 11474N
  169338. 2/28/96V
  169339. G. SEYHOLD, FLASH THERMOLYSIS OF ORGANIC COMPOUNDS, 16, 366 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169340. GABRIEL WEATHERHEAD
  169341. 10466
  169342. 11475N
  169343. 2/28/96V
  169344. H. J. BESTMANN, PHOSPHACUMULENE YLIDS AND PHOSPHAALLENE YLIDS, 16, 349 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169345. GABRIEL WEATHERHEAD
  169346. 10467
  169347. 11476N
  169348. 2/28/96
  169349. U. SCHOLLKOPF, RECENT APPLIEATIONS OF ALPHA METALATED ISOCYANIDES IN ORGANIC SYNTHESIS, 16, 339 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169350. GABRIEL WEATHERHEAD
  169351. 10468
  169352. 11477N
  169353. 2/28/96V
  169354. B. GIESE, BASIS AND LIMITATIONS OF THE REACTIVITY SELECTIVITY PRINCIPLE, 16,126 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169355. GABRIEL WEATHERHEAD
  169356. 10469
  169357. 11478N
  169358. 2/28/96VtM. I. BRUCE, CYCLOMETALATION REACTIONS, 16, 73 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169359. GABRIEL WEATHERHEAD
  169360. 10470
  169361. 11479N
  169362. 2/28/96V
  169363. W. OPPOLZER, INTRAMOLECULAR [4 + 2] AND [3 + 2] CYCLOADDITIONS IN ORGANIC SYNTHESIS, 16,10 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169364. GABRIEL WEATHERHEAD
  169365. 10471
  169366. 11480N
  169367. 2/28/96V{H. WERNER, NEW VARIETIES OF SANDWICH COMPOUNDS, 16, 1 (1977). ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  169368. GABRIEL WEATHERHEAD
  169369. 10472
  169370. 11481N
  169371. 2/28/96VuK. A. KIME AND R. E. SIEVERS PRAETICAL GUIDE TO LANTHANIDE SHIFT REAGENTS, 10, 64 (1977). ALDRICHIMICA ACTA A REVIEW.a
  169372. GABRIEL WEATHERHEAD
  169373. 10473
  169374. 11482N
  169375. 2/28/96VbC. F. LANE, SELECTIVE REDUCTIONS WITH BORANE COMPLEXES, 10, 41 (1977). ALDRICHIMICA ACTA A REVIEW.a
  169376. GABRIEL WEATHERHEAD
  169377. 10474
  169378. 11483N
  169379. 2/28/96VII. C. P. SMITH, DEUTERIUM NMR, 10, 35 (1977). ALDRICHIMICA ACTA A REVIEW.a
  169380. GABRIEL WEATHERHEAD
  169381. 10475
  169382. 11484N
  169383. 2/28/96VQW. A. SZABO, CHLOROSULFONYL ISOCYANATE, 10 23 (1977). ALDRICHIMICA ACTA A REVIEW.a
  169384. GABRIEL WEATHERHEAD
  169385. 10476
  169386. 11485N
  169387. 2/28/96V
  169388. A. BRANDSTROM, PRINCIPLES OF PHASE TRANSFER CATALYSIS BY QUATERNARY AMMONIUM SALTS, 15, 267 (1977). ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  169389. GABRIEL WEATHERHEAD
  169390. 10477
  169391. 11486N
  169392. 2/28/96V}T. E. HOGEN ESCH, ION PAIRING EFFECTS IN CARBANION REACTIONS, 15,154 (1977). ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.
  169393. GABRIEL WEATHERHEAD
  169394. 10478
  169395. 11487N
  169396. 2/28/96V
  169397. J. M. THOMAS AND (IN PART) S. E. MORSI AND J. P. DESVERGNE, TOPOCHEMICAL PHENOMENA IN ORGANIC SOLID STATE CHEMISTRY, 15, 64 (1977). ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  169398. GABRIEL WEATHERHEAD
  169399. 10479
  169400. 11488N
  169401. 2/28/96VnJ. HINE, THE PRINCIPLE OF LEAST NUCLEAR MOTION, 15, 1 (1977). ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  169402. GABRIEL WEATHERHEAD
  169403. 10480
  169404. 11489N
  169405. 2/28/96V
  169406. F. C. DE SCHRYVER, N. BOENS, AND J. PUT, EXCITED STATE BEHAVIOR OF SOME BICHROMOPHORIC SYSTEMS, 10, 359 (1977). ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  169407. GABRIEL WEATHERHEAD
  169408. 10481
  169409. 11490N
  169410. 2/28/96V
  169411. W. KLOPFFER, INTRAMOLECULAR PROTON TRANSFER IN ELECTRONICALLY EXCITED MOLECULES, 10, 311(1977). ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  169412. GABRIEL WEATHERHEAD
  169413. 10482
  169414. 11491N
  169415. 2/28/96
  169416. C. R. BOCK AND E. A. K. VON GUSTORF, PRIMARY PHOTOPROCESSES OF ORGANO TRANSITION METAL COMPOUNDS, 10, 221 (1977) . ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  169417. GABRIEL WEATHERHEAD
  169418. 10483
  169419. 11492N
  169420. 2/28/96V|R. B. CUNDALL AND L. C. PEREIRA, EXEITATION AND DEEXCITATION OF BENZENE, 10,147 (1977). ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  169421. GABRIEL WEATHERHEAD
  169422. 10484
  169423. 11493N
  169424. 2/28/96V
  169425. C. VON SONNTAG AND H. P. SEHUCHMANN, PHOTOLYSIS OF SATURATED ALCOHOLS, ETHERS, AND AMINES, 10, 59 (1977). ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  169426. GABRIEL WEATHERHEAD
  169427. 10485
  169428. 11494N
  169429. 2/28/96V
  169430. J. EVANS, MOLECULAR REARRANGEMENTS IN POLYNUELEAR TRANSITION METAL COMPLEXES, 16, 319 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169431. GABRIEL WEATHERHEAD
  169432. 10486
  169433. 11495N
  169434. 2/28/96VjT. J. KATZ, THE OLEFIN METATHESIS REACTION, 16, 283 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169435. GABRIEL WEATHERHEAD
  169436. 10487
  169437. 11496N
  169438. 2/28/96
  169439. M. TSUTSUI AND A. COURTNEY, SIGMA PI REARRANGEMENTS OF ORGANOTRANSITION METAL COMPOUNDS, 16, 241(1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169440. GABRIEL WEATHERHEAD
  169441. 10488
  169442. 11497N
  169443. 2/28/96V
  169444. J. W. FALLER, FLUXIONAL AND NONRIGID BEHAVIOR OF TRANSITION METAL ORGANOMETALLIC PI COMPLEXES, 16, 211 (1977) ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169445. GABRIEL WEATHERHEAD
  169446. 10489
  169447. 11498N
  169448. 2/28/96V
  169449. E. GROVENSTEIN, JR. ARYL MIGRATIONS IN ORGANOMETALLIC COMPOUNDS OF THE ALKALI METALS, 16,167 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169450. GABRIEL WEATHERHEAD
  169451. 10490
  169452. 11499N
  169453. 2/28/96ViE. A. HILL, ORGANOMAGNESIUM REARRANGEMENTS, 16,131 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169454. GABRIEL WEATHERHEAD
  169455. 10491
  169456. 11500N
  169457. 2/28/96V
  169458. J. P. OLIVER, REARRANGEMENTS OF ORGANOALUMINUM COMPOUNDS AND THEIR GROUP III ANALOGS, 16,111(1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169459. GABRIEL WEATHERHEAD
  169460. 10492
  169461. 11501N
  169462. 2/28/96V
  169463. J. J. EISCH, REARRANGEMENT OF UNSATURATED ORGANOBORON AND ORGANOALUMINUM COMPOUNDS, 16, 67 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169464. GABRIEL WEATHERHEAD
  169465. 10493
  169466. 11502N
  169467. 2/28/96V
  169468. M. T. REETZ, DYOTROPIC REARRANGEMENTS AND RELATED EXCHANGE PROCESSES, 16, 33 (1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169469. GABRIEL WEATHERHEAD
  169470. 10494
  169471. 11503N
  169472. 2/28/96V
  169473. R. WEST, 1,2 ANIONIC REARRANGEMENTS OF ORGANOSILICON AND GERMANIUM COMPOUNDS, 16,1(1977). ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  169474. GABRIEL WEATHERHEAD
  169475. 10495
  169476. 11504N
  169477. 2/28/96VfW. ADAM, THE CHEMISTRY OF 1,2 DIOXETANES, 21, 438 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169478. GABRIEL WEATHERHEAD
  169479. 10496
  169480. 11505N
  169481. 2/28/96VrR. N. BUTLER, RECENT ADVANCES IN TETRAZOLE CHEMISTRY, 21, 324 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169482. GABRIEL WEATHERHEAD
  169483. 10497
  169484. 11506N
  169485. 2/28/96
  169486. D. N. REINHOUDT, (2 + 2) CYCLOADDITION AND (2 + 2) CYCLOREVERSION REACTIONS OF HETEROCYCLIC COMPOUNDS, 21, 254 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169487. GABRIEL WEATHERHEAD
  169488. 10498
  169489. 11507N
  169490. 2/28/96VzY. TAKEUCHI AND F. FURUSAKI, THE CHEMISTRY OF ISOXAZOLIDINES, 21, 208 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169491. GABRIEL WEATHERHEAD
  169492. 10499
  169493. 11508N
  169494. 2/28/96V
  169495. R. FILLER AND Y. S. RAO, NEW DEVELOPMENTS IN THE CHEMISTRY OF OXAZOLONES, 21,176 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169496. GABRIEL WEATHERHEAD
  169497. 10500
  169498. 11509N
  169499. 2/28/96V
  169500. F. FRINGUELLI, G. MARINO, AND A. TATICCHI, TELLUROPHENE AND RELATED COMPOUNDS, 21,120 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169501. GABRIEL WEATHERHEAD
  169502. 10501
  169503. 11510N
  169504. 2/28/96V^J. M. BARKER, THE THIENOPYRIDINES, 21, 65 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169505. GABRIEL WEATHERHEAD
  169506. 10502
  169507. 11511N
  169508. 2/28/96
  169509. D. E. KUHLA AND J. G. LOMBARDINO, PYRROLODIAZINES WITH A BRIDGEHEAD NITROGEN, 21, 2 (1977). ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  169510. GABRIEL WEATHERHEAD
  169511. 10503
  169512. 11512N
  169513. 2/28/96V
  169514. R. F. HECK TRANSITION METAL CATALYZED REACTIONS OF ORGANIC HALIDES WITH CO, OLEFINS, AND ACETYLENES, 26, 323 (1977). ADVANCES IN CATALYSIS A REVIEW.a
  169515. GABRIEL WEATHERHEAD
  169516. 10504
  169517. 11513N
  169518. 2/28/96VlA. K. GALWEY COMPENSATION EFFECT IN HETEROGENEOUS CATALYSIS, 26, 247 (1977). ADVANCES IN CATALYSIS A REVIEW.a
  169519. GABRIEL WEATHERHEAD
  169520. 10505
  169521. 11514N
  169522. 2/28/96V
  169523. J. A. DUMESIC AND H. TOPSOE, MOSSBAUER SPECTROSCOPY APPLICATIONS TO HETEROGENEOUS CATALYSIS, 26,122 (1977). ADVANCES IN CATALYSIS A REVIEW.a
  169524. GABRIEL WEATHERHEAD
  169525. 10506
  169526. 11515N
  169527. 2/28/96V
  169528. W. M. H. SACHTLER AND R. A. VAN SANIEN, SURFACE COMPOSITION AND SELECTIVITY OF ALLOY CATALYSTS, 26, 69 (1977). ADVANCES IN CATALYSIS A REVIEW.a
  169529. GABRIEL WEATHERHEAD
  169530. 10507
  169531. 11516N
  169532. 2/28/96
  169533. VfG. A. SOMORJAI, ACTIVE SITES IN HETEROGENEOUS CATALYSIS, 26, 2 (1977). ADVANCES IN CATALYSIS A REVIEW.a
  169534. GABRIEL WEATHERHEAD
  169535. 10508
  169536. 11517N
  169537. 2/28/96V
  169538. G. A. JEFFREY AND M. SUNDARALINGAM, BIBLIOGRAPHY OF CRYSTAL STRUCTURES OF CARBOHYDRATES, NUCLEOSIDES, AND NUCLEOTIDES, 1975, 34, 345 (1977). ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  169539. GABRIEL WEATHERHEAD
  169540. 10509
  169541. 11518N
  169542. 2/28/96V
  169543. M. CHEN AND R. L. WHISTLER, METABOLISM OF D FRUCTOSE, 34, 286 (1977). ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  169544. GABRIEL WEATHERHEAD
  169545. 10510
  169546. 11519N
  169547. 2/28/96VwK. IGARASHI, THE KOENIGS KNORR REACTION, 34, 243 .(1977). ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  169548. GABRIEL WEATHERHEAD
  169549. 10511
  169550. 11520N
  169551. 2/28/96V
  169552. A. N. DE BELDER, CYCLIC ACETALS OF THE ALDOSES AND ALDOSIDES, 34,179 (1977). ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  169553. GABRIEL WEATHERHEAD
  169554. 10512
  169555. 11521N
  169556. 2/28/96V
  169557. M. CERNY AND J. STANEK, JR., 1,6 ANHYDRO DERIVATIVES OF ALDOHEXOSES, 34, 24 (1977). ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  169558. GABRIEL WEATHERHEAD
  169559. 10513
  169560. 11522N
  169561. 2/28/96V
  169562. T. H. CHAN, ALKENE SYNTHESIS VIA ,B FUNCTIONALIZED ORGANOSILICON COMPOUNDS, 10, 442 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169563. GABRIEL WEATHERHEAD
  169564. 10514
  169565. 11523N
  169566. 2/28/96VpW. M. JONES, CARBENE CARBENE REARRANGEMENTS IN SOLUTION, 10, 353 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169567. GABRIEL WEATHERHEAD
  169568. 10515
  169569. 11524N
  169570. 2/28/96V
  169571. I. SAITO, T. MATSUURA, M. NAKAGAWA, AND T. HINO, PEROXIDIC INTERMEDIATES IN PHOTOSENSITIZED OXYGENATION OF TRYPTOPHAN DERIVATIVES, 10, 346 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169572. GABRIEL WEATHERHEAD
  169573. 10516
  169574. 11525N
  169575. 2/28/96
  169576. J. B. HENDRICKSON, D. D. STERNBACH, AND K. W. BAIR, TRIFLUOROMETHYLSULFONYL ACTIVATION IN ORGANIC SYNTHESIS, 10, 306 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169577. GABRIEL WEATHERHEAD
  169578. 10517
  169579. 11526N
  169580. 2/28/96V
  169581. V. J. NOWLAN AND T. T. TIDWELL, STRUCTURAL EFFECTS ON THE ACID CATALYZED HYDRATION OF ALKENES, 10, 252 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169582. GABRIEL WEATHERHEAD
  169583. 10518
  169584. 11527N
  169585. 2/28/96V
  169586. S. M. HECHT, UTILIZATION OF ISOMERIC AMINOACYL TRANSFER RIBONUCLEIC ACIDS IN PEPTIDE BOND FORMATION, 10, 239 ( 1977) . ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169587. GABRIEL WEATHERHEAD
  169588. 10519
  169589. 11528N
  169590. 2/28/96V
  169591. F. E. ZIEGLER, STEREO  AND REGIOCHEMISTRY OF THE CLAISEN REARRANGEMENT: APPLICATIONS TO NATURAL PRODUCTS SYNTHESIS, 10, 227 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169592. GABRIEL WEATHERHEAD
  169593. 10520
  169594. 11529N
  169595. 2/28/96
  169596. VuR. HUISGEN, CAN TETRAMETHYLENE INTERMEDIATES BE INTERCEPTED ?, 10,199 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169597. GABRIEL WEATHERHEAD
  169598. 10521
  169599. 11530N
  169600. 2/28/96VmR. V. STEVENS, GENERAL METHODS OF ALKALOID SYNTHESIS, 10, 193 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169601. GABRIEL WEATHERHEAD
  169602. 10522
  169603. 11531N
  169604. 2/28/96V
  169605. P. BEAK, ENERGIES AND ALKYLATIONS OF TAUTOMERIC HETEROCYCLIC COMPOUNDS: OLD PROBLEMS
  169606. NEW ANSWERS, 10, 186 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169607. GABRIEL WEATHERHEAD
  169608. 10523
  169609. 11532N
  169610. 2/28/96V
  169611. W. ANDO, YLIDE FORMATION AND REARRANGEMENT IN THE REACTION OF CARBENE WITH DIVALENT SULFUR COMPOUNDS, 10, 179 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169612. GABRIEL WEATHERHEAD
  169613. 10524
  169614. 11533N
  169615. 2/28/96
  169616. G. BARTOLI AND P. E. TODESCO, NUCLEOPHILIC SUBSTITUTION. LINEAR FREE ENERGY RELATIONSHIPS BETWEEN REACTIVITY AND PHYSICAL PROPERTIES OF LEAVING GROUPS AND SUBSTRATES, 10, 125 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169617. GABRIEL WEATHERHEAD
  169618. 10525
  169619. 11534N
  169620. 2/28/96V
  169621. R. HUISGEN, TETRACYANOETHYLENE AND ENOL ETHERS. A MODEL FOR 2 + 2 CYCLOADDITIONS VIA ZWITTERIONIC INTERMEDIATES, 10 117 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169622. GABRIEL WEATHERHEAD
  169623. 10526
  169624. 11535N
  169625. 2/28/96V
  169626. H. D. ROTH, CHEMICALLY INDUCED NUCLEAR SPIN POLARIZATION IN THE STUDY OF CARBENE REACTION MECHANISMS, 10, 85 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169627. GABRIEL WEATHERHEAD
  169628. 10527
  169629. 11536N
  169630. 2/28/96ViR. E. MOORE, VOLATILE COMPOUNDS FROM MARINE ALGAE, 10, 40 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169631. GABRIEL WEATHERHEAD
  169632. 10528
  169633. 11537N
  169634. 2/28/96VTP. J. SCHEUER, MARINE TOXINS, 10, 33 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.
  169635. GABRIEL WEATHERHEAD
  169636. 10529
  169637. 11538N
  169638. 2/28/96V
  169639. E. WASSERMAN AND R. S. HUTTON, EPR OF TRIPLET STATES: CYCLIC 4 PI ELECTRON SYSTEMS, CH2, AND ENVIRONMENTAL EFFECTS, 10, 27 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169640. GABRIEL WEATHERHEAD
  169641. 10530
  169642. 11539N
  169643. 2/28/96V
  169644. R. KH. FREIDLINA AND A. B. TERENT'EV, FREE RADICAL REARRANGEMENTS IN TELOMERIZATION, 10, 9 (1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169645. GABRIEL WEATHERHEAD
  169646. 10531
  169647. 11540N
  169648. 2/28/96V
  169649. K. P. C. VOLLHARDT, TRANSITION METAL CATALYZED ACETYLENE CYCLIZATIONS IN ORGANIC SYNTHESIS, 10,1(1977). ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  169650. GABRIEL WEATHERHEAD
  169651. 10532
  169652. 11541N
  169653. 2/28/96VnWEISS, U; EDWARDS, J. M. THE BIOSYNTHESIS OF AROMATIC COMPOUNDS; WILEY LNTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  169654. GABRIEL WEATHERHEAD
  169655. 10533
  169656. 11542N
  169657. 2/28/96
  169658. GROS, J. J. C.; BOUREIER, S. ABSOLUTE CONFIGURATIONS OF 6000 SELECTED COMPOUNDS WITH ONE ASYMMETRIC CARBON ATOM (STEREOCHEMISTRY, FUNDAMENTALS AND METHODS, VOL. 4); THIEME VERLAG: STUTTGART, 1977. A REVIEW.a
  169659. GABRIEL WEATHERHEAD
  169660. 10534
  169661. 11543N
  169662. 2/28/96VeGRIFFITHS, J. COLOUR AND CONSTITUTION OF ORGANIC MOLECULES; ACADEMIC PRESS: NEW YORK, 1977. A REVIEW.a
  169663. GABRIEL WEATHERHEAD
  169664. 10535
  169665. 11544N
  169666. 2/28/96VVEPIOTIS, N. D. THEORY OF ORGANIC REACTIONS; SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  169667. GABRIEL WEATHERHEAD
  169668. 10536
  169669. 11545N
  169670. 2/28/96VYBLOCK, E. REACTIONS OF ORGANOSULPHUR COMPOUNDS, ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  169671. GABRIEL WEATHERHEAD
  169672. 10537
  169673. 11546N
  169674. 2/28/96V]BENDER, M. L.; KOMIYAMA, M. CYCLODEXTRIN CHEMISTRY SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  169675. GABRIEL WEATHERHEAD
  169676. 10538
  169677. 11547N
  169678. 2/28/96VWBAILEY, P. S. OZONATION IN ORGANIC CHEMISTRY, ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.
  169679. GABRIEL WEATHERHEAD
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  169683. SCHWARZ, H. SOME NEW ASPECTS OF MASS SPECTROMETRIC ORTHO EFFECTS. 1978, 73, 231. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978 A REVIEW.a
  169684. GABRIEL WEATHERHEAD
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  169687. 2/28/96V
  169688. JUTZ, J. C. AROMATIC AND HETEROAROMATIC COMPOUNDS BY ELECTROCYCLIC RING CLOSURE WITH ELIMINATION. 1978, 73,125. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978 A REVIEW.a
  169689. GABRIEL WEATHERHEAD
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  169693. CAUBERE, P. COMPLEX BASES AND COMPLEX REDUCING AGENTS. NEW TOOLS IN ORGANIC SYNTHESIS. 1978, 73, 49. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978 A REVIEW.a
  169694. GABRIEL WEATHERHEAD
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  169697. 2/28/96V
  169698. SHELDRICK, W. S. STEREOCHEMISTRY OF PENTA  AND HEXACOORDINATE PHOSPHORUS DERIVATIVES. 1978, 73,1. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978 A REVIEW.a
  169699. GABRIEL WEATHERHEAD
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  169702. 2/28/96
  169703. SMALLEY, R. K. HALOGENOQUINOLINES. QUINOLINE AND ITS DERIVATIVES, PART 1. G. JONES, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE: NEW YORK, 1977 A REVIEW.a
  169704. GABRIEL WEATHERHEAD
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  169707. 2/28/96V
  169708. JONES, G. SYNTHESIS OF THE QUINOLINE RING SYSTEM. QUINOLINE AND ITS DERIVATIVES, PART 1. G. JONES, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE: NEW YORK, 1977 A REVIEW.a
  169709. GABRIEL WEATHERHEAD
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  169713. JONES, G. PHYSICAL AND CHEMICAL PROPERTIES OF QUINOLINE. QUINOLINE AND ITS DERIVATIVES, PART 1. G. JONES, ED. (CHEMISTRY OF HETEROCYCLIC COMPOUNDS), WILEY INTERSCIENCE: NEW YORK, 1977 A REVIEW.a
  169714. GABRIEL WEATHERHEAD
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  169717. 2/28/96
  169718. FIAUD, J. C. DETERMINATION OF ABSOLUTE CONFIGURATIONS BY ASYMMETRIC SYNTHESIS, BY RESOLUTION, AND BY ENZYMIC METHODS. DETERMINATION OF CONFIGURATIONS BY CHEMICAL METHODS (VOL. 3, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.
  169719. GABRIEL WEATHERHEAD
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  169723. HOREAU, A. DETERMINATION OF THE CONFIGURATION OF SECONDARY ALCOHOLS BY PARTIAL RESOLUTION. DETERMINATION OF CONFIGURATIONS BY CHEMICAL METHODS (VOL. 3, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.a
  169724. GABRIEL WEATHERHEAD
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  169728. FIAUD, J. C.; KAGAN, H. B. DETERMINATIONS OF STEREOCHEMISTRY BY CHEMICAL CORRELATION METHODS. DETERMINATION OF CONFIGURATIONS BY CHEMICAL METHODS (VOL. 3, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART,1977 A REVIEW.a
  169729. GABRIEL WEATHERHEAD
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  169733. LEGRAND, M.; ROUGIER, M. J. APPLICATIONS OF OPTICAL ACTIVITY TO STEREOCHEMICAL DETERMINATIONS. DETERMINATION OF CONFIGURATIONS BY DIPOLE MOMENTS, CD OR ORD (VOL. 2, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.
  169734. GABRIEL WEATHERHEAD
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  169738.     MINKIN, V. I. DIPOLE MOMENTS AND STEREOCHEMISTRY OF ORGANIC COMPOUNDS. SELECTED APPLICATIONS. DETERMINATION OF CONFIGURATIONS BY DIPOLE MOMENTS, CD OR ORD (VOL. 2, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.
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  169743. PARTHASARATHY, R. DETERMINATION OF RELATIVE AND ABSOLUTE CONFIGURATIONS OF ORGANIC MOLECULES BY X RAY. DETERMINATION OF CONFIGURATIONS BY SPECTROPHOTOMETRIC METHODS (VOL. 1, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.
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  169748. MANDELBAUM, A. APPLICATION OF MASS SPECTROMETRY TO STEREOCHEMICAL PROBLEMS. DETERMINATION OF CONFIGURATIONS BY SPECTROPHOTOMETRIC METHODS (VOL. 1, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.a
  169749. GABRIEL WEATHERHEAD
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  169753. GAUDEMER, A. RELATIVE CONFIGURATIONS BY NMR SPECTROSCOPY. DETERMINATION OF CONFIGURATIONS BY SPECTROPHOTOMETRIC METHODS (VOL. 1, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.a
  169754. GABRIEL WEATHERHEAD
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  169758. GOLFIER, M. DETERMINATION OF CONFIGURATIONS BY INFRARED SPECTROSCOPY. DETERMINATION OF CONFIGURATIONS BY SPECTROPHOTOMETRIC METHODS (VOL. 1, STEREOCHEMISTRY FUNDAMENTALS AND METHODS, H. B. KAGAN, ED.), THIEME VERLAG: STUTTGART, 1977 A REVIEW.a
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  169763. AKHTAR, M.; JONES, C. BIOLOGICAL TRANSFORMATIONS INVOLVING UNSATURATED LINKAGES: CHARGE SEPARATION AND NEUTRALIZATION IN ENZYME CATALYSIS. 1978, 34, 813. TETRAHEDRON A REVIEW.a
  169764. GABRIEL WEATHERHEAD
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  169767. 2/28/96V^GRUNDON, M. F. THE BIOSYNTHESIS OF AROMATIC HEMITERPENES, 1978, 34, 143. TETRAHEDRON A REVIEW.a
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  169771. 2/28/96VpRIPOLL, J. L.; ROUESSAC, F. RECENT APPLICATIONS OF THE DIELS ALDER REACTION. 1978, 34, 19. TETRAHEDRON A REVIEW.a
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  169775. 2/28/96VnSCHLOSSER, M. INTRODUCTION OF FLUORINE INTO ORGANIC MOLECULES: WHY AND HOW. 1978, 34, 3. TETRAHEDRON A REVIEW.a
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  169779. 2/28/96VtROSSI, R. INSECT PHEROMONES; II. SYNTHESIS OF CHIRAL COMPONENTS OF INSECT PHEROMONES. 1978, 413. SYNTHESIS A REVIEW.a
  169780. GABRIEL WEATHERHEAD
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  169784. VMVALENTINE, JR., J. W. S. ASYMMETRIC SYNTHESIS. 1978, 329. SYNTHESIS A REVIEW.a
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  169788. 2/28/96ViFATIADI, A. J. NEW APPLICATIONS OF MALONONITRILE IN ORGANIC CHEMISTRY. 1978,165, 241. SYNTHESIS A REVIEW.a
  169789. GABRIEL WEATHERHEAD
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  169792. 2/28/96VnKRAPCHO, A. P. SYNTHESIS OF CARBOCYCLIC SPIRO COMPOUNDS VIA CYCLOADDITION ROUTE. 1978, 77. SYNTHESIS A REVIEW.a
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  169797. SCHMIDT, A. H., RIED, W. SYNTHESIS OF CYCLOBUTENEDIONE AND ITS ALKYL, ALKENYL AND ARYL DERIVATIVES. 1978,1. SYNTHESIS A REVIEW.a
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  169802. ANDRIANOV, K. A.; EMEL'YANOV, V. N. ORGANOSILOXAZANES
  169803. A NEW LINE OF ADVANCE IN THE CHEMISTRY OF HETERO ORGANIC OLIGOMERS AND POLYMERS. 1977, 46,1092. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169804. GABRIEL WEATHERHEAD
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  169808. VvFOKIN, A. V.; UZUN, A. T.; STOLYAROV, V. P. ORGANIC N FLUOROIMINES. 1977, 46, 1057. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169809. GABRIEL WEATHERHEAD
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  169813. REUTOV, O. A.; KURTS, A. L. ADVANCES IN THE CHEMISTRY OF AMBIDENT ENOLATE AND PHENOXIDE LONS. 1977, 46,1040. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169814. GABRIEL WEATHERHEAD
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  169818. NEFEDOV, O. M.; D'YACHENKO, A. I., PROKOF'EV, A. K. ARYNES AND CARBENES DERIVED FROM ORGANOELEMENT COMPOUNDS. 1977, 46, 941. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169819. GABRIEL WEATHERHEAD
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  169823. LAZURIN, E. A., VORONENKOV, V. V., OSOKIN YU. G. THE MECHANISM AND STEREOCHEMISTRY OF THE OXIDATION OF BICYCLIC HYDROCARBONS WITH A BRIDGE BOND. 1977, 46, 915. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169824. GABRIEL WEATHERHEAD
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  169828. ALEKSANDROV, YU. A.; TARUNIN, B. I. OXIDATION BY OZONE OF HETERO ORGANIC COMPOUNDS OF THE SILICON SUBGROUP. 1977, 46, 905. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169829. GABRIEL WEATHERHEAD
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  169833. BELEN'KII, L. I.; VOL'KENSHTEIN, YU. B.; KARMANOVA, I. B. NEW DATA ON THE CHLOROMETHYLATION OF AROMATIC AND HETEROAROMATIC COMPOUNDS. 1977, 46, 891. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169834. GABRIEL WEATHERHEAD
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  169838. IOFFE, S. L., LEONT'EVA, L. M., TARTAKOVSKII, V. A. CHEMISTRY OF ALPHA NITROHETERO ORGANIC COMPOUNDS. 1977, 46, 872. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169839. GABRIEL WEATHERHEAD
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  169843. KRASIL'NIKOVA, E. A. STRUCTURE AND REACTIVITY OF ESTERS OF THIO ACIDS OF THREE COORDINATED PHOSPHORUS. 1977, 46, 861. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169844. GABRIEL WEATHERHEAD
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  169848. VwBOKANOV, A. I.; STPANOV, B. I. CHEMISTRY OF DIHYDROPHENOPHOSPHAZINES. 1977, 46, 855. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
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  169852. 2/28/96VqBEL'SKII, V. E. KINETICS OF THE HYDROLYSIS OF PHOSPHATE ESTERS. 1977, 46, 828. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169853. GABRIEL WEATHERHEAD
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  169857. ARSHINOVA, R. P. THE KERR EFFECT AND THE STRUCTURE OF ORGANOPHOSPHORUS COMPOUNDS. 1977, 46, 809. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169858. GABRIEL WEATHERHEAD
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  169862. ZVEREV, V. V.; KITAEV, YU. T. THE PHOTOELECTRON SPECTROSCOPY OF ORGANOPHOSPHORUS COMPOUNDS. 1977, 46, 791. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169863. GABRIEL WEATHERHEAD
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  169867. PLISKO, E. A., NUD'GA, L A., DANILOV, S. N. CHITIN AND ITS CHEMICAL TRANSFORMATIONS. 1977, 46, 764. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169868. GABRIEL WEATHERHEAD
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  169872. VxSTRUNIN, B. N. CHEMICAL TRANSFORMATIONS OF AMINOGLYCOSIDE ANTIBIOTICS. 1977, 46, 749. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
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  169876. 2/28/96VnSKARCHENKO, V. K. OXIDATIVE DEHYDROGENATION OL HYDROCARBONS. 1977, 46, 731. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169877. GABRIEL WEATHERHEAD
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  169881. SARYBAEVA, R. I.; AFANAS'EV, V. A., ZAIKOV, G. E., SHCHELOKHOVA, L. S. THE APPLICATIONS OF LEWIS ACIDS IN CARBOHYDRATE CHEMISTRY. 1977, 46, 722. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169882. GABRIEL WEATHERHEAD
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  169886. TEL'NOI, V. I., RABINOVICH, I. B. THERMOCHEMISTRY OF ORGANIC COMPOUNDS OF TRANSITION METALS. 1977, 46, 689. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169887. GABRIEL WEATHERHEAD
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  169890. 2/28/96VkORLOV, YU. E. POLAROGRAPHY OF COUMARINS (CHROMEN 2 ONES). 1977, 46, 671. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169891. GABRIEL WEATHERHEAD
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  169895. VtAVETISYAN, A. A.; DANGYAN, M. T. THE CHEMISTRY OF DAB BUTENOLIDES. 1977, 46, 643. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169896. GABRIEL WEATHERHEAD
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  169900. MAZUR, I. A.; MANDRICHENKO, B. E.; KATKEVICH, R. T. METHODS OF SYNTHESIS OF IMIDAZOPYRIMIDINES WITH A BRIDGEHEAD NITROGEN ATOM AND THEIR BENZO ANALOGS. 1977, 46, 634. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169901. GABRIEL WEATHERHEAD
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  169905. ANSHELES, V. R.; PIS'MAN, I. I. THE REACTIONS OF MONOOLEFINS IN THE PRESENCE OF ALKALI METALS AND THEIR DERIVATIVES. 1977, 46, 620. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  169906. GABRIEL WEATHERHEAD
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  169909. 2/28/96V{HOWARTH, 0. W.; LILLEY, D. M. J. CARBON 13 NMR OF PEPTIDES AND PROTEINS. 1978,12, 1. PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
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  169913. 2/28/96VvCHAKRABORTY, D. P. CARBAZOLE ALKALOIDS. 1977, 34, 300. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.
  169914. GABRIEL WEATHERHEAD
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  169918. OVERTON, K. H.; PICKEN, D. J. SECONDARY METABOLISM WITH PLANT TISSUE CULTURES. 1977, 34, 249. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
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  169923. GROSS, D. PHYTOALEXINE AND RELATED PLANT SUBSTANCES (IN GER.). 1977, 34, 187. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  169924. GABRIEL WEATHERHEAD
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  169928. PINDER, A. R. CHEMISTRY OF EREMOPHILANE AND RELATED SESQUITERPENES. 1977, 34, 81. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  169929. GABRIEL WEATHERHEAD
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  169933. ENZELL, C. R., WAHLBERG, I., AASEN, A. J. ISOPRENOIDS AND ALKALOIDS OF TOBACCO. 1977, 34 PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  169934. GABRIEL WEATHERHEAD
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  169938. SCHMIDT, M. BIFUNCTIONAL THIOETHERS AS COMPLEX LIGANDS WITH D 8 METALS. 1978, 4, 239. PHOSPHORUS AND SULFUR AND THE RELATED ELEMENTS A REVIEW.a
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  169943. OKAFOR, C. O. CHEMISTRY AND BIOLOGICAL ACTIVITY OF NEW AZAPHENOTHIAZINES, THIAPHENOTHIAZINES AND DIBENZOTHIAZEPINES. 1978, 4, 79. PHOSPHORUS AND SULFUR AND THE RELATED ELEMENTS A REVIEW.a
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  169947. 2/28/96VtNAGATA, W.; YOSHIOKA, M. HYDROCYANATION OF CONJUGATED CARBONYL COMPOUNDS. 1977, 25, 255. ORGANIC REACTIONS A REVIEW.a
  169948. GABRIEL WEATHERHEAD
  169949. 10595
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  169951. 2/28/96VwWADSWORTH, JR., W. S. SYNTHETIC APPLICATIONS OF PHOSPHORYL STABILIZED ANIONS. 1977, 25, 73. ORGANIC REACTIONS A REVIEW.a
  169952. GABRIEL WEATHERHEAD
  169953. 10596
  169954. 11605N
  169955. 2/28/96V\PAQUETTE, L. A. THE RAMBERG BACKLUND REARRANGEMENT. 1977, 25, 1. ORGANIC REACTIONS A REVIEW.a
  169956. GABRIEL WEATHERHEAD
  169957. 10597
  169958. 11606N
  169959. 2/28/96
  169960. VxWEBER, W. P., GOKEL, G. W. PHASE TRANSFER CATALYSIS APPLICATIONS. 1978, 54, 429. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  169961. GABRIEL WEATHERHEAD
  169962. 10598
  169963. 11607N
  169964. 2/28/96VwHO, T. L. ANALYSIS OF SYNTHETIC REACTIONS BY THE HSAB PRINCIPLE. 1978, 54, 355. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  169965. GABRIEL WEATHERHEAD
  169966. 10599
  169967. 11608N
  169968. 2/28/96V
  169969. GOKEL, G. W.; WEBER, W. P. PHASE TRANSFER CATALYSIS. GENERAL PRINCIPLES. 1978, 54, 350. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  169970. GABRIEL WEATHERHEAD
  169971. 10600
  169972. 11609N
  169973. 2/28/96V~CHENIER, P. J. FAVORSKII REARRANGEMENT IN BRIDGED POLYCYCLIC COMPOUNDS. 1978, 54, 286. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  169974. GABRIEL WEATHERHEAD
  169975. 10601
  169976. 11610N
  169977. 2/28/96V
  169978. BRAGG, R. W., CHOW, Y.; DENNIS, L., FERGUSON, L. N.; HOWELL, S.; MORGA, G.; OGINO, C.; PUGH, H.; WINTERS, M. SWEET ORGANIC CHEMISTRY. 1978, 54, 281. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  169979. GABRIEL WEATHERHEAD
  169980. 10602
  169981. 11611
  169982. 2/28/96VtBOIS CHOUSSY, M.; BARBIER, M. ISOMERIZATIONS AND CYCLIZATIONS IN BILE PIGMENTS. 1978, 9, 677. HETEROCYCLES A REVIEW.a
  169983. GABRIEL WEATHERHEAD
  169984. 10603
  169985. 11612N
  169986. 2/28/96V
  169987. TOURWE, D., VAN BINST, G. CARBON 13 NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY OF QUINOLIZIDINE DERIVATIVES. 1978, 9, 507. HETEROCYCLES A REVIEW.a
  169988. GABRIEL WEATHERHEAD
  169989. 10604
  169990. 11613N
  169991. 2/28/96VxKAMETANI, T., TAKAHASHI, K. SYNTHESIS OF PYRROLO[1,2 A]INDOLES AND RELATED SYSTEMS. 1978, 9, 293. HETEROCYCLES A REVIEW.a
  169992. GABRIEL WEATHERHEAD
  169993. 10605
  169994. 11614N
  169995. 2/28/96V
  169996. VAN DER PLAS, H. C. RING MODIFYING REACTIONS OF PYRIMIDINES CONTAINING A QUATERNARY NITROGEN. 1978, 9, 33. HETEROCYCLES A REVIEW.a
  169997. GABRIEL WEATHERHEAD
  169998. 10606
  169999. 11615N
  170000. 2/28/96V
  170001. TILAK, B. D.; GOGTE, V. N. SYNTHESES AND REARRANGEMENTS OF SOME FOUR MEMBERED HETEROCYCLIC COMPOUNDS. 1977, 7, 1339. HETEROCYCLES A REVIEW.a
  170002. GABRIEL WEATHERHEAD
  170003. 10607
  170004. 11616N
  170005. 2/28/96
  170006. ViVOLZ, H.; KOWARSCH, H. HETEROPENTALENES AND HETEROCYCLIC FERROCENES. 1977, 7,1319. HETEROCYCLES A REVIEW.a
  170007. GABRIEL WEATHERHEAD
  170008. 10608
  170009. 11617N
  170010. 2/28/96ViDESLONGCHAMPS, P. STEREOELECTRONIC CONTROL IN HYDROLYTIC REACTIONS. 1977, 7, 1271. HETEROCYCLES A REVIEW.a
  170011. GABRIEL WEATHERHEAD
  170012. 10609
  170013. 11618N
  170014. 2/28/96V
  170015. BOSE, A. K.; MANHAS, M. S.; TAVARES, R. F., VAN DER VEEN, J. M.; FUJIWARA, H. NON BONDED ATTRACTION AND THE CONFORMATION OF AROMATIC AMINO ACID DERIVATIVES. 1977, 7, 1227. HETEROCYCLES A REVIEW.a
  170016. GABRIEL WEATHERHEAD
  170017. 10610
  170018. 11619N
  170019. 2/28/96VzVAN BOOM, J. H. SYNTHESIS OF OLIGORIBONUCLEOTIDES VIA PHOSPHOTRIESTER INTERMEDIATES. 1977, 7, 1197. HETEROCYCLES A REVIEW.a
  170020. GABRIEL WEATHERHEAD
  170021. 10611
  170022. 11620N
  170023. 2/28/96V
  170024. MIZUMO, Y., IKEDA, K.; ENDO, T.; TSUCHIDA, K. AROMATIC AMINE N OXIDES IN SYNTHESES OF NUCLEOSIDES AND NUCLEOTIDES. 1977, 7, 1189 HETEROCYCLES A REVIEW.a
  170025. GABRIEL WEATHERHEAD
  170026. 10612
  170027. 11621N
  170028. 2/28/96
  170029. VbSCARTAZZINI, R.; BICKEL, H. NEW ORALLY ACTIVE CEPHALOSPORINS. 1977, 7 1165. HETEROCYCLES A REVIEW.a
  170030. GABRIEL WEATHERHEAD
  170031. 10613
  170032. 11622N
  170033. 2/28/96V]AKIBA, K. Y.; INAMOTO, N. CHEMISTRY OF N NITROSOIMINES. 1977, 7, 1131. HETEROCYCLES A REVIEW.a
  170034. GABRIEL WEATHERHEAD
  170035. 10614
  170036. 11623N
  170037. 2/28/96V
  170038. TAKAMIZAWA, A.; MATSUMOTO, S., IWATA, T.; MAKINO, I. CHEMISTRY OF C4 FUNCTIONALIZED 1,3,2 0XAZAPHOSPHORINANE 2 0XIDES RELATED TO THE ACTIVE METABOLITE OF CYCLOPHOSPHAMIDE. 1977, 7, 1091 HETEROCYCLES A REVIEW.a
  170039. GABRIEL WEATHERHEAD
  170040. 10615
  170041. 11624N
  170042. 2/28/96V^YAKHONTOV, L. RECENT ADVANCES IN QUINUCLIDINE CHEMISTRY. 1977, 7, 1033. HETEROCYCLES A REVIEW.a
  170043. GABRIEL WEATHERHEAD
  170044. 10616
  170045. 11625N
  170046. 2/28/96VeGALPIN, I. CHEMICAL SYNTHESES OF PEPTIDES AND PROTEINS. 1978, 14, 181. CHEMISTRY IN BRITAIN A REVIEW.a
  170047. GABRIEL WEATHERHEAD
  170048. 10617
  170049. 11626N
  170050. 2/28/96
  170051. VVTHOMPSON, R. H. MARINE NATURAL PRODUCTS. 1978, 14, 133. CHEMISTRY IN BRITAIN A REVIEW.a
  170052. GABRIEL WEATHERHEAD
  170053. 10618
  170054. 11627N
  170055. 2/28/96VoHELLER, H. G. PHOTOCHROMIC COMPOUNDS FOR OPTICAL INFORMATION STORES. 1978,193. CHEMISTRY AND INDUSTRY A REVIEW.a
  170056. GABRIEL WEATHERHEAD
  170057. 10619
  170058. 11628N
  170059. 2/28/96VaLAIRD, T. ENERGY STORAGE VIA PHOTOCHEMICAL REACTIONS. 1978, 186. CHEMISTRY AND INDUSTRY A REVIEW.a
  170060. GABRIEL WEATHERHEAD
  170061. 10620
  170062. 11629N
  170063. 2/28/96V`DAVIDSON, R. S. PRACTICAL ASPECTS OF PHOTOCHEMISTRY. 1978, 180. CHEMISTRY AND INDUSTRY A REVIEW.a
  170064. GABRIEL WEATHERHEAD
  170065. 10621
  170066. 11630N
  170067. 2/28/96V[COLVIN, E. W. SILICON IN ORGANIC SYNTHESIS. 1978, 7, 15. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170068. GABRIEL WEATHERHEAD
  170069. 10622
  170070. 11631N
  170071. 2/28/96V
  170072. GIBSON, K. H. PROSTAGLANDINS, THROMBOXANES, PGX: BIOSYNTHETIC PRODUCTS FROM ARACHIDONIC ACID. 1977, 6, 489. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170073. GABRIEL WEATHERHEAD
  170074. 10623
  170075. 11632
  170076. 2/28/96V{SANDERS, J. K. M. NMR SPECTRAL CHANGE AS A PROBE OF CHLOROPHYLL CHEMISTRY. 1977, 6, 467. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170077. GABRIEL WEATHERHEAD
  170078. 10624
  170079. 11633N
  170080. 2/28/96VuCRAMMER, B.; IKAN, R. PROPERTIES AND SYNTHESES OF SWEETENING AGENTS. 1977, 6, 431. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170081. GABRIEL WEATHERHEAD
  170082. 10625
  170083. 11634N
  170084. 2/28/96V
  170085. WIESNER, K. STRATEGY IN THE SYNTHESIS OF POLYCYCLIC POLYSUBSTITUTED NATURAL PRODUCTS: THE ACONITE ALKALOIDS. 1977, 6, 413. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170086. GABRIEL WEATHERHEAD
  170087. 10626
  170088. 11635N
  170089. 2/28/96V
  170090. CRAGG, G. M. L.; KOCH K R. ORGANOBORATES IN ORGANIC SYNTHESIS: THE USE OF ALKENYL , ALKYNYL , AND CYANO BORATES AS SYNTHETIC INTERMEDIATES. 1977, 6, 393. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170091. GABRIEL WEATHERHEAD
  170092. 10627
  170093. 11636N
  170094. 2/28/96V~BEAK, P.; REITZ, D. B. DIPOLE STABILIZED CARBANIONS: NOVEL AND USEFUL INTERMEDIATES. 1978, 78, 275. CHEMICAL REVIEWS A REVIEW.a
  170095. GABRIEL WEATHERHEAD
  170096. 10628
  170097. 11637N
  170098. 2/28/96V
  170099. CHOW, Y. L.; DANEN, W. C.; NELSEN, S. F., ROSENBLATT, D. H. NONAROMATIC AMINIUM RADICALS. 1978, 78, 243. CHEMICAL REVIEWS A REVIEW.a
  170100. GABRIEL WEATHERHEAD
  170101. 10629
  170102. 11638N
  170103. 2/28/96V
  170104. PIATAK, D. M.; WICHA, J. VARIOUS APPROACHES TO THE CONSTRUCTION OF ALIPHATIC SIDE CHAINS OF STEROIDS AND RELATED COMPOUNDS. 1978, 78,199. CHEMICAL REVIEWS A REVIEW.a
  170105. GABRIEL WEATHERHEAD
  170106. 10630
  170107. 11639N
  170108. 2/28/96V
  170109. TURRO, N. J., RAMAMURTHY, V.; CHERRY, W.; FARNETH, W. THE EFFECT OF WAVELENGTH ON ORGANIC PHOTOREACTIONS IN SOLUTION. REACTIONS FROM UPPER EXCITED STATES. 1978, 78, 125. CHEMICAL REVIEWS A REVIEW.a
  170110. GABRIEL WEATHERHEAD
  170111. 10631
  170112. 11640N
  170113. 2/28/96VdCOYLE, J. D. PHOTOCHEMISTRY OF CARBOXYLIC ACID DERIVATIVES. 1978, 78, 97. CHEMICAL REVIEWS A REVIEW.a
  170114. GABRIEL WEATHERHEAD
  170115. 10632
  170116. 11641N
  170117. 2/28/96
  170118. V}CAMPBELL, M. M.; JOHNSON, G. CHLORAMINE T AND RELATED N HALOGENO N METALLO REAGENTS. 1978, 78, 65. CHEMICAL REVIEWS A REVIEW.a
  170119. GABRIEL WEATHERHEAD
  170120. 10633
  170121. 11642N
  170122. 2/28/96V
  170123. KEANA, J. F. W. NEWER ASPECTS OF THE SYNTHESIS AND CHEMISTRY OF NITROXIDE SPIN LABELS. 1978, 78, 37. CHEMICAL REVIEWS A REVIEW.a
  170124. GABRIEL WEATHERHEAD
  170125. 10634
  170126. 11643N
  170127. 2/28/96V
  170128. BENSON, S. W. THERMOCHEMISTRY AND KINETICS OF SULFUR CONTAINING MOLECULES AND RADICALS. 1978, 78, 23. CHEMICAL REVIEWS A REVIEW.a
  170129. GABRIEL WEATHERHEAD
  170130. 10635
  170131. 11644N
  170132. 2/28/96V
  170133. HANACK, M. MECHANISTIC AND PREPARATIVE ASPECTS OF VINYL CATION CHEMISTRY. 1978,17, 333. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170134. GABRIEL WEATHERHEAD
  170135. 10636
  170136. 11645N
  170137. 2/28/96V
  170138. GROVENSTEIN JR., E. SKELETAL REARRANGEMENTS OF ORGANOALKALI METAL COMPOUNDS. 1978,17, 313. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170139. GABRIEL WEATHERHEAD
  170140. 10637
  170141. 11646
  170142. 2/28/96V
  170143. NICOLAOU, K. C.; GASIC, G. P.; BARNETTE, W. E. PROSTAGLANDIN ENDOPEROXIDES, THROMBOXANES, AND PROSTACYCLINS. 1978, 17, 293. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170144. GABRIEL WEATHERHEAD
  170145. 10638
  170146. 11647N
  170147. 2/28/96VsLASZLO, P. SODIUM 23 NMR SPECTROSCOPY. 1978, 17, 254. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170148. GABRIEL WEATHERHEAD
  170149. 10639
  170150. 11648N
  170151. 2/28/96V
  170152. KLEMPERER W. G. 17O NMR SPECTROSCOPY AS A STRUCTURAL PROBE. 1978, 17, 246. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170153. GABRIEL WEATHERHEAD
  170154. 10640
  170155. 11649N
  170156. 2/28/96V
  170157. MASON, R.; MEEK, D. W. TERTIARY PHOSPHINE LIGANDS IN ORGANOMETALLIC CHEMISTRY. 1978,17, 204. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170158. GABRIEL WEATHERHEAD
  170159. 10641
  170160. 11650N
  170161. 2/28/96
  170162. IZUMI, Y.; CHIBATA, I.; ITOH T. PRODUCTION AND UTILIZATION OF AMINO ACIDS. 1978,17, 176. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170163. GABRIEL WEATHERHEAD
  170164. 10642
  170165. 11651N
  170166. 2/28/96V
  170167. YAMAMOTO, H., NOZAKI, H. SELECTIVE REACTIONS WITH ORGANOALUMINUM COMPOUNDS. 1978,17, 169. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170168. GABRIEL WEATHERHEAD
  170169. 10643
  170170. 11652N
  170171. 2/28/96V
  170172. KAUPP, G. PHOTOCHEMICAL REARRANGEMENTS AND FRAGMENTATIONS OF ALKENES AND POLYENES. 1978,17, 150. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170173. GABRIEL WEATHERHEAD
  170174. 10644
  170175. 11653N
  170176. 2/28/96V
  170177. ZOLLINGER, H. NITROGEN AS LEAVING GROUP: DEDIAZONIATION OF AROMATIC DIAZONIUM LONS. 1978,17, 141. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170178. GABRIEL WEATHERHEAD
  170179. 10645
  170180. 11654N
  170181. 2/28/96
  170182. PAQUETTE, L. A. THE REALITIES OF EXTENDED HOMOAROMATICITY. 1978, 17, 106. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170183. GABRIEL WEATHERHEAD
  170184. 10646
  170185. 11655N
  170186. 2/28/96V
  170187. LAROCK, R. C. ORGANOMERCURY COMPOUNDS IN ORGANIC SYNTHESIS. 1978,17, 27. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170188. GABRIEL WEATHERHEAD
  170189. 10647
  170190. 11656N
  170191. 2/28/96V
  170192. FISCHER, M. INDUSTRIAL APPLICATIONS OF PHOTOCHEMICAL SYNTHESES. 1978,17, 16. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170193. GABRIEL WEATHERHEAD
  170194. 10648
  170195. 11657N
  170196. 2/28/96V\BESCHKE, H. REACTIONS OF 2,3 CYCLOALKENOPYRIDINES, 1978, 11, 13. ALDRICHIMICA ACTA A REVIEW.a
  170197. GABRIEL WEATHERHEAD
  170198. 10649
  170199. 11658N
  170200. 2/28/96V
  170201. CHEESEMAN, G. W. H.; WERSTIUK, E. S. G. QUINOXALINE CHEMISTRY: DEVELOPMENTS 1963 1975.1978, 22, 368. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170202. GABRIEL WEATHERHEAD
  170203. 10650
  170204. 11659N
  170205. 2/28/96
  170206. FLITSCH, W.; KRAMER, U. CYCLAZINES AND RELATED N BRIDGED ANNULENES. 1978, 22, 322. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170207. GABRIEL WEATHERHEAD
  170208. 10651
  170209. 11660N
  170210. 2/28/96V
  170211. ELGUERO, J.; CLARAMUNT, R. M.; SUMMERS, A. J. H. THE CHEMISTRY OF AROMATIC AZAPENTALENES. 1978, 22, 184. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170212. GABRIEL WEATHERHEAD
  170213. 10652
  170214. 11661N
  170215. 2/28/96VpHIREMATH, S. P.; HOOPER, M. ISATOGENS AND INDOLONES. 1978, 22, 124. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170216. GABRIEL WEATHERHEAD
  170217. 10653
  170218. 11662N
  170219. 2/28/96V
  170220. ZOLTEWICZ, J. A.; DEADY L. W. QUATERNIZATION OF HETEROAROMATIC COMPOUNDS: QUANTITATIVE ASPECTS. 1978, 22, 72. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170221. GABRIEL WEATHERHEAD
  170222. 10654
  170223. 11663N
  170224. 2/28/96V]SUMMERS, L. A. THE PHENANTHROLINES. 1978, 22, 2. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  170225. GABRIEL WEATHERHEAD
  170226. 10655
  170227. 11664N
  170228. 2/28/96
  170229. VsMISUMI, S.; OTSUBO, T. CHEMISTRY OF MULTILAYERED CYCLOPHANES. 1978,11, 251. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170230. GABRIEL WEATHERHEAD
  170231. 10656
  170232. 11665N
  170233. 2/28/96VsBILLUPS, W. E. SYNTHESIS AND CHEMISTRY OF BENZOCYCLOPROPANES. 1978,11, 245. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170234. GABRIEL WEATHERHEAD
  170235. 10657
  170236. 11666N
  170237. 2/28/96V
  170238. RAMIREZ, F.; MARACEK, J. F. PHOSPHORYLATION BY MEANS OF CYCLIC ENEDIOL PHOSPHATES. 1978,11, 239. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170239. GABRIEL WEATHERHEAD
  170240. 10658
  170241. 11667N
  170242. 2/28/96V
  170243. SAREL, S. METAL INDUCED REARRANGEMENTS AND INSERTIONS INTO CYCLOPROPYL OLEFINS. 1978, 11, 204. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170244. GABRIEL WEATHERHEAD
  170245. 10659
  170246. 11668N
  170247. 2/28/96V
  170248. KOBAYASHI, Y.; KUMADAKI, I. REACTIONS OF AROMATIC TRIFLUOROMETHYL COMPOUNDS WITH NUCLEOPHILIC REAGENTS. 1978, 11, 197. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170249. GABRIEL WEATHERHEAD
  170250. 10660
  170251. 11669N
  170252. 2/28/96
  170253. VbASHE, III, A. J. THE GROUP 5 HETEROBENZENES. 1978,11, 153. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170254. GABRIEL WEATHERHEAD
  170255. 10661
  170256. 11670N
  170257. 2/28/96V
  170258. BERNASCONI, C. F. KINETIC BEHAVIOR OF SHORT LIVED ANIONIC SIGMA COMPLEXES. 1978, 11, 147 .ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170259. GABRIEL WEATHERHEAD
  170260. 10662
  170261. 11671N
  170262. 2/28/96V
  170263. RABIDEAU, P. W. THE CONFORMATIONAL ANALYSIS OF 1,4 CYCLOHEXADIENES, 1,4 DIHYDROBENZENES, 1,4 DIHYDRONAPHTHALENES, AND 9,10 DIHYDROANTHRACENES. 1978,11,141. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170264. GABRIEL WEATHERHEAD
  170265. 10663
  170266. 11672N
  170267. 2/28/96V}STANG, P. J. VINYL TRIFLATE CHEMISTRY: UNSATURATED CATIONS AND CARBENES. 1978,11,107. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170268. GABRIEL WEATHERHEAD
  170269. 10664
  170270. 11673N
  170271. 2/28/96V
  170272. SCHUSTER, D. I. MECHANISMS OF PHOTOCHEMICAL TRANSFORMATIONS OF CROSS CONJUGATED CYCLOHEXADIENONES. 1978,11, 65. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170273. GABRIEL WEATHERHEAD
  170274. 10665
  170275. 11674N
  170276. 2/28/96V
  170277. JOHNSON, M. D. REACTIONS OF ELECTROPHILES WITH SIGMA BONDED ORGANOTRANSITION METAL COMPLEXES. 1978,11, 57. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170278. GABRIEL WEATHERHEAD
  170279. 10666
  170280. 11675N
  170281. 2/28/96V
  170282. LEHN, J. M. CRYPTATES: THE CHEMISTRY OF MACROPOLYCYCLIC INCLUSION COMPLEXES. 1978,11, 49. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170283. GABRIEL WEATHERHEAD
  170284. 10667
  170285. 11676N
  170286. 2/28/96V
  170287. GOLD, V.; MCADAM, M. E. RADIATION LNDUCED ORGANIC HYDROGEN ISOTOPE EXCHANGE REACTIONS IN AQUEOUS SOLUTION. 1978, 1L, 36. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170288. GABRIEL WEATHERHEAD
  170289. 10668
  170290. 11677N
  170291. 2/28/96V
  170292. SCOTT, A. I. BIOSYNTHESIS OF VITAMIN BL2 IN SEARCH OF THE PORPHYRIN CORRIN CONNECTION. 1978 11, 29. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170293. GABRIEL WEATHERHEAD
  170294. 10669
  170295. 11678N
  170296. 2/28/96VyPORTOGHESE, P. S. STEREOISOMERIC LIGANDS AS OPIOID RECEPTOR PROBES. 1978, 11, 21. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170297. GABRIEL WEATHERHEAD
  170298. 10670
  170299. 11679N
  170300. 2/28/96V{NELSEN, S. CONFORMATIONAL STUDIES OF HEXAHYDROPYRIDAZINE DERIVATIVES. 1978, 11, 14. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170301. GABRIEL WEATHERHEAD
  170302. 10671
  170303. 11680N
  170304. 2/28/96V
  170305. CRAM, D. J; CRAM, J. M. DESIGN OF COMPLEXES BETWEEN SYNTHETIC HOSTS AND ORGANIC GUESTS. 1978,11, 8. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170306. GABRIEL WEATHERHEAD
  170307. 10672
  170308. 11681N
  170309. 2/28/96V
  170310. HINE, J. BIFUNCTIONAL CATALYSIS OF ALPHA HYDROGEN EXCHANGE OF ALDEHYDES AND KETONES. 1978,11, 1. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  170311. GABRIEL WEATHERHEAD
  170312. 10673
  170313. 11682N
  170314. 2/28/96VTYATES, K. HUCKEL MOLECULAR ORBITAL THEORY; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170315. GABRIEL WEATHERHEAD
  170316. 10674
  170317. 11683N
  170318. 2/28/96VcTURRO, N. MODERN MOLECULAR PHOTOCHEMISTRY BENJAMIN/CUMMINGS: MENLO PARK, CALIFORNIA 1978. A REVIEW.a
  170319. GABRIEL WEATHERHEAD
  170320. 10675
  170321. 11684N
  170322. 2/28/96
  170323. (V]STARKS, C. M.; LIOTTA, C. PHASE TRANSFER CATALYSIS, ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170324. GABRIEL WEATHERHEAD
  170325. 10676
  170326. 11685N
  170327. 2/28/96VgSHAMMA, M.; MONIOT, J. L. ISOQUINOLINE ALKALOIDS RESEARCH: 1972 1977; PLENUM: NEW YORK, 1978. A REVIEW.a
  170328. GABRIEL WEATHERHEAD
  170329. 10677
  170330. 11686N
  170331. 2/28/96VdPATAI, S., ED. CHEMISTRY OF DIAZONIUM AND DIAZO GROUPS WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170332. GABRIEL WEATHERHEAD
  170333. 10678
  170334. 11687N
  170335. 2/28/96VnPATAI, S., ED. CHEMISTRY OF CYANATES AND THEIR THIO DERIVATIVES; WILEY INTERSCIENCE: NEW YORK, 1977. A REVIEW.a
  170336. GABRIEL WEATHERHEAD
  170337. 10679
  170338. 11688N
  170339. 2/28/96VhNORMAN, R. O. C. PRINCIPLES OF ORGANIC SYNTHESIS, 2ND ED.; WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170340. GABRIEL WEATHERHEAD
  170341. 10680
  170342. 11689N
  170343. 2/28/96
  170344. NEUNHOFFER, H.; WILEY, P. F. CHEMISTRY OF 1,2,3 TRIAZINES AND 1,2,4 TRIAZINES, TETRAZINES AND PENTAZINES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 33); WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170345. GABRIEL WEATHERHEAD
  170346. 10681
  170347. 11690N
  170348. 2/28/96V]MURRELL, J. N.; TEDDER, J. M. THE CHEMICAL BOND WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170349. GABRIEL WEATHERHEAD
  170350. 10682
  170351. 11691N
  170352. 2/28/96V
  170353. KLYNE, W.; BUCKINGHAM, J. ATLAS OF STEREOCHEMISTRY
  170354.  ABSOLUTE CONFIGURATIONS OF ORGANIC MOLECULES, 2ND ED., VOLS. 1 AND 2, OXFORD UNIVERSITY PRESS: NEW YORK 1978. A REVIEW.a
  170355. GABRIEL WEATHERHEAD
  170356. 10683
  170357. 11692N
  170358. 2/28/96VcGREENBERG, A., LIEBMAN, J. F. STRAINED ORGANIC MOLECULES; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170359. GABRIEL WEATHERHEAD
  170360. 10684
  170361. 11693N
  170362. 2/28/96VjFREIFELDER, M. CATALYTIC HYDROGENATION IN ORGANIC SYNTHESIS; WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170363. GABRIEL WEATHERHEAD
  170364. 10685
  170365. 11694N
  170366. 2/28/96
  170367. FRAY, G. I.; SAXTON, R. G. THE CHEMISTRY OF CYCLOOCTATETRAENE AND ITS DERIVATIVES, CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, 1978. A REVIEW.a
  170368. GABRIEL WEATHERHEAD
  170369. 10686
  170370. 11695N
  170371. 2/28/96VoDOLPHIN, D., ED. THE PORPHYRINS, VOL. 5, PHYSICAL CHEMISTRY, PART C., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170372. GABRIEL WEATHERHEAD
  170373. 10687
  170374. 11696N
  170375. 2/28/96VsDOLPHIN, D., ED. THE PORPHYRINS. VOL. 2, STRUCTURE AND SYNTHESIS, PART B; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170376. GABRIEL WEATHERHEAD
  170377. 10688
  170378. 11697N
  170379. 2/28/96VsDOLPHIN, D., ED. THE PORPHYRINS, VOL. 1, STRUCTURE AND SYNTHESIS, PART A; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170380. GABRIEL WEATHERHEAD
  170381. 10689
  170382. 11698N
  170383. 2/28/96VlDAVIES, D. I.; PARROTT, M. J. FREE RADICALS IN ORGANIC SYNTHESIS, SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  170384. GABRIEL WEATHERHEAD
  170385. 10690
  170386. 11699N
  170387. 2/28/96VCCORBRIDGE, D. E. C. PHOSPHORUS; ELSEVIER, NEW YORK, 1978. A REVIEW.a
  170388. GABRIEL WEATHERHEAD
  170389. 10691
  170390. 11700N
  170391. 2/28/96VsCARRUTHERS, W. MODERN METHODS OF ORGANIC SYNTHESIS, 2ND ED.; CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, 1978. A REVIEW.a
  170392. GABRIEL WEATHERHEAD
  170393. 10692
  170394. 11701N
  170395. 2/28/96V
  170396. ALPER, H. OXIDATION, REDUCTION, REARRANGEMENT, AND OTHER SYNTHETICALLY USEFUL PROCESSES. TRANSITION METAL ORGANOMETALLICS IN ORGANIC SYNTHESIS (VOL. 2, H. ALPER, ED.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170397. GABRIEL WEATHERHEAD
  170398. 10693
  170399. 11702N
  170400. 2/28/96V
  170401. JAOUEN, G. ARENE COMPLEXES IN ORGANIC SYNTHESIS. TRANSITION METAL ORGANOMETALLICS IN ORGANIC SYNTHESIS (VOL. 2, H. ALPER, ED.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170402. GABRIEL WEATHERHEAD
  170403. 10694
  170404. 11703N
  170405. 2/28/96
  170406.  NICHOLAS, K. M.; NESTLE, M. O.; SEYFERTH, D. THE POTENTIAL UTILITY OF TRANSITION METAL ALKYNE COMPLEXES AND DERIVED CLUSTER COMPOUNDS AS REAGENTS IN ORGANIC SYNTHESIS. TRANSITION METAL ORGANOMETALLICS IN ORGANIC SYNTHESIS (VOL. 2, H. ALPER, ED.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.
  170407. GABRIEL WEATHERHEAD
  170408. 10695
  170409. 11704N
  170410. 2/28/96V
  170411. KOCH, T. H. ET AL. PHOTOCHEMICAL REACTIVITY OF KETO IMINO ETHERS. 1978, 75, 65. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  170412. GABRIEL WEATHERHEAD
  170413. 10696
  170414. 11705N
  170415. 2/28/96V
  170416. LEWIS, E. S. ISOTOPE EFFECTS IN HYDROGEN ATOM TRANSFERS. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  170417. GABRIEL WEATHERHEAD
  170418. 10697
  170419. 11706N
  170420. 2/28/96V
  170421. VOGTLE, F.; HOHNER, G. MULTIBRIDGED MULTILAYERED AND MULTISTEPPED ORGANIC COMPOUNDS. L978, 74, 1. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1978. A REVIEW.a
  170422. GABRIEL WEATHERHEAD
  170423. 10698
  170424. 11707
  170425. 2/28/96V
  170426. SCHWIND, R. A.; GILLIGAN, T. J.; GUSSIER, E. L. DEVELOPING THE COMMERCIAL POTENTIAL OF MACROCYCLIC MOLECULES. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170427. GABRIEL WEATHERHEAD
  170428. 10699
  170429. 11708N
  170430. 2/28/96V
  170431. LIESEGANG, G. W.; EYRING, E. M. KINETIC STUDIES OF SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170432. GABRIEL WEATHERHEAD
  170433. 10700
  170434. 11709N
  170435. 2/28/96V
  170436. DALLEY, N. K. STRUCTURAL STUDIES OF SYNTHETIC MACROCYCLIC MOLECULES AND THEIR CATION COMPLEXES. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170437. GABRIEL WEATHERHEAD
  170438. 10701
  170439. 11710N
  170440. 2/28/96
  170441. LIOTTA, C. L. APPLICATION OF MACROCYCLIC POLYDENTATE LIGANDS TO SYNTHETIC TRANSFORMATIONS. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170442. GABRIEL WEATHERHEAD
  170443. 10702
  170444. 11711N
  170445. 2/28/96V
  170446. BRADSHAW, J. S. SYNTHESIS OF MULTIDENTATE COMPOUNDS. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170447. GABRIEL WEATHERHEAD
  170448. 10703
  170449. 11712N
  170450. 2/28/96V
  170451. PEDERSEN, C. J. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS. SYNTHETIC MULTIDENTATE MACROCYCLIC COMPOUNDS, R. M. IZATT AND J. J. CHRISTENSEN, EDS., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170452. GABRIEL WEATHERHEAD
  170453. 10704
  170454. 11713N
  170455. 2/28/96V
  170456. HOUK, K. N. THEORY OF REACTIVE INTERMEDIATES AND REACTION MECHANISM. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170457. GABRIEL WEATHERHEAD
  170458. 10705
  170459. 11714N
  170460. 2/28/96V
  170461. GASPAR, P. P. SILYLENES. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170462. GABRIEL WEATHERHEAD
  170463. 10706
  170464. 11715N
  170465. 2/28/96V
  170466. LWOWSKI, W. NITRENES. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170467. GABRIEL WEATHERHEAD
  170468. 10707
  170469. 11716N
  170470. 2/28/96V
  170471. KAPLAN, L. FREE RADICALS. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170472. GABRIEL WEATHERHEAD
  170473. 10708
  170474. 11717N
  170475. 2/28/96V
  170476. BETHELL, D. CARBOCATIONS. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170477. GABRIEL WEATHERHEAD
  170478. 10709
  170479. 11718N
  170480. 2/28/96V
  170481. MOSS, R. A.; JONES, JR. M. CARBENES REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170482. GABRIEL WEATHERHEAD
  170483. 10710
  170484. 11719N
  170485. 2/28/96V
  170486. IE NOBLE, W. J. CARBANIONS. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170487. GABRIEL WEATHERHEAD
  170488. 10711
  170489. 11720N
  170490. 2/28/96V
  170491. LEVIN, R. H. ARYNES. REACTIVE INTERMEDIATES (VOL. 1, M. JONES AND R. A. MOSS, EDS.), WILEY INTERSCIENCE: NEW YORK, 1978. A REVIEW.a
  170492. GABRIEL WEATHERHEAD
  170493. 10712
  170494. 11721N
  170495. 2/28/96V
  170496. CHAKRABARTTY, S. K. ALKALINE HYPOHALITE OXIDATIONS. OXIDATION IN ORGANIC CHEMISTRY, PART C. W. S. TRAHANOVSKY, ED., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170497. GABRIEL WEATHERHEAD
  170498. 10713
  170499. 11722N
  170500. 2/28/96V
  170501. OGATA, Y. OXIDATIONS WITH NITRIC ACID OR NITROGEN OXIDES. OXIDATION IN ORGANIC CHEMISTRY, PART C. W. S. TRAHANOVSKY, ED., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170502. GABRIEL WEATHERHEAD
  170503. 10714
  170504. 11723N
  170505. 2/28/96
  170506. PLESNICAR, B. OXIDATIONS WITH PEROXY ACIDS AND OTHER PEROXIDES. OXIDATION IN ORGANIC CHEMISTRY, PART C. W. S. TRAHANOVSKY, ED., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170507. GABRIEL WEATHERHEAD
  170508. 10715
  170509. 11724N
  170510. 2/28/96V
  170511. JOHNSON, R. A. OXYGENATIONS WITH MICROORGANISMS. OXIDATION IN ORGANIC CHEMISTRY, PART C. W. S. TRAHANOVSKY, ED., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170512. GABRIEL WEATHERHEAD
  170513. 10716
  170514. 11725N
  170515. 2/28/96V
  170516. REICH, H. J. ORGANOSELENIUM OXIDATIONS. OXIDATION IN ORGANIC CHEMISTRY, PART C. W. S. TRAHANOVSKY, ED., ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170517. GABRIEL WEATHERHEAD
  170518. 10717
  170519. 11726N
  170520. 2/28/96V
  170521. LANDESBERG, J. M. STABILIZING OF UNSTABLE SPECIES WITH CARBONYLIRON. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170522. GABRIEL WEATHERHEAD
  170523. 10718
  170524. 11727N
  170525. 2/28/96
  170526. KING, R. B. MONOOLEFIN, ALLYL AND DIENE IRON COMPLEXES. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170527. GABRIEL WEATHERHEAD
  170528. 10719
  170529. 11728N
  170530. 2/28/96V
  170531. BOWDEN, F. L.; WOOD, L. H. COMPOUNDS WITH IRON CARBON SIGMA BONDS. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170532. GABRIEL WEATHERHEAD
  170533. 10720
  170534. 11729N
  170535. 2/28/96V
  170536. BRUNNER, HENRI. OPTICAL ACTIVITY. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170537. GABRIEL WEATHERHEAD
  170538. 10721
  170539. 11730N
  170540. 2/28/96
  170541. KONIG, E. MAGNETIC PROPERTIES AND EPR. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170542. GABRIEL WEATHERHEAD
  170543. 10722
  170544. 11731N
  170545. 2/28/96V
  170546. PARISH, R. V. MOSSBAUER SPECTROSCOPY. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170547. GABRIEL WEATHERHEAD
  170548. 10723
  170549. 11732N
  170550. 2/28/96V
  170551. MULLER, J. MASS SPECTRA. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170552. GABRIEL WEATHERHEAD
  170553. 10724
  170554. 11733N
  170555. 2/28/96
  170556. MARKS, T. J. NMR SPECTROSCOPY OF ORGANOIRON COMPOUNDS. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  170557. GABRIEL WEATHERHEAD
  170558. 10725
  170559. 11734N
  170560. 2/28/96
  170561. KRUGER, C.; BARNETT, B. L.; BRAUER, D, STRUCTURE AND BONDING IN ORGANIC IRON COMPOUNDS. THE ORGANIC CHEMISTRY OF IRON (VOL. 1, ORGANOMETALLIC CHEMISTRY, THE LATE E. A. K. VON GUSTORF, F. W. GREVELS, I. FISCHLER, EDS.), ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.
  170562. GABRIEL WEATHERHEAD
  170563. 10726
  170564. 11735N
  170565. 2/28/96V
  170566. BENOITON, N. L. N OMEGA ALKYLDIAMINO ACIDS: CHEMISTRY AND PROPERTIES. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS (VOL. 5, B. WEINSTEIN, ED.), MARCEL DEKKER: NEW YORK, 1978 A REVIEW.a
  170567. GABRIEL WEATHERHEAD
  170568. 10727
  170569. 11736N
  170570. 2/28/96
  170571. SMEBY, R. R.; FERMANDJIAN, S. CONFORMATION OF ANGIOTENSIN II. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS (VOL. 5, B. WEINSTEIN, ED.), MARCEL DEKKER: NEW YORK, 1978 A REVIEW.a
  170572. GABRIEL WEATHERHEAD
  170573. 10728
  170574. 11737N
  170575. 2/28/96V
  170576. HALPERN. R. APPLICATION OF ALDEHYDE AND KETONE CONDENSATES AS PROTECTING GROUPS IN PEPTIDE CHEMISTRY. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS (VOL. 5, B. WEINSTEIN, ED.), MARCEL DEKKER: NEW YORK, 1978 A REVIEW.a
  170577. GABRIEL WEATHERHEAD
  170578. 10729
  170579. 11738N
  170580. 2/28/96V
  170581. DARFLER, F. J.; TOMETSKO, A. M. APPLICATIONS OF LIGHT SENSITIVE  CHEMICALS FOR PROBING BIOLOGICAL PROCESSES. CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS (VOL. 5, B. WEINSTEIN, ED.), MARCEL DEKKER: NEW YORK, 1978 A REVIEW.a
  170582. GABRIEL WEATHERHEAD
  170583. 10730
  170584. 11739N
  170585. 2/28/96VdSULLIVAN, G. R. CHIRAL LANTHANIDE SHIFT REAGENTS. 1977, 10, 287. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  170586. GABRIEL WEATHERHEAD
  170587. 10731
  170588. 11740N
  170589. 2/28/96VsKAGAN, H. B.; FIAUD, J. C. NEW APPROACHES IN ASYMMETRIC SYNTHESIS. 1977,10,175. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  170590. GABRIEL WEATHERHEAD
  170591. 10732
  170592. 11741N
  170593. 2/28/96ViSAITO, Y. ABSOLUTE STEREOCHEMISTRY OF CHELATE COMPLEXES 1977, 10, 95. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  170594. GABRIEL WEATHERHEAD
  170595. 10733
  170596. 11742N
  170597. 2/28/96V`FUCHS, B. CONFORMATIONS OF FIVE MEMBERED RINGS. 1977, 10, 1. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  170598. GABRIEL WEATHERHEAD
  170599. 10734
  170600. 11743N
  170601. 2/28/96V
  170602. GANEM, B. FROM GLUCOSE TO AROMATICS: RECENT DEVELOPMENTS IN NATURAL PRODUCTS OF THE SHIKIMIC ACID PATHWAY. 1978, 34, 3353. TETRAHEDRON A REVIEW.a
  170603. GABRIEL WEATHERHEAD
  170604. 10735
  170605. 11744N
  170606. 2/28/96VyMACKIEWICZ, P.; FURSTOSS, R. AMIDYL RADICALS; STRUCTURE AND REACTIVITY (IN FRENCH). 1978, 34, 3241. TETRAHEDRON A REVIEW.a
  170607. GABRIEL WEATHERHEAD
  170608. 10736
  170609. 11745N
  170610. 2/28/96
  170611. REESE, C. B. THE CHEMICAL SYNTHESIS OF OLIGO  AND POLY NUCLEOTIDES BY THE PHOSPHOTRIESTER APPROACH. 1978. 34, 3143. TETRAHEDRON A REVIEW.a
  170612. GABRIEL WEATHERHEAD
  170613. 10737
  170614. 11746N
  170615. 2/28/96V
  170616. DAVIES. S. G.; GREEN, M. L. H.; MINGOS, D. M. P. NUCLEOPHILIC ADDITION TO ORGANOTRANSITION METAL CATIONS CONTAINING UNSATURATED HYDROCARBON LIGANDS. A SURVEY AND INTERPRETATION. 1978, 34 , 3047. TETRAHEDRON A REVIEW.a
  170617. GABRIEL WEATHERHEAD
  170618. 10738
  170619. 11747N
  170620. 2/28/96VuREUTOV, O. A. SOME ASPECTS OF ORGANOMETALLIC CHEMISTRY OF NONTRANSITION METALS. 1978, 34, 3827. TETRAHEDRON A REVIEW.a
  170621. GABRIEL WEATHERHEAD
  170622. 10739
  170623. 11748N
  170624. 2/28/96VeBECK, J. R. NUCLEOPHILIC DISPLACEMENT OF AROMATIC NITRO GROUPS. 1978, 34, 2057. TETRAHEDRON A REVIEW.a
  170625. GABRIEL WEATHERHEAD
  170626. 10740
  170627. 11749N
  170628. 2/28/96V
  170629. TIDWELL, T. T. STERICALLY CROWDED ORGANIC MOLECULES: SYNTHESIS, STRUCTURE AND PROPERTIES, 1978, 34, 1855. TETRAHEDRON A REVIEW.a
  170630. GABRIEL WEATHERHEAD
  170631. 10741
  170632. 11750N
  170633. 2/28/96VjMUKERJEE, A. K.; SINGH, A. K. BETA LACTAMS: RETROSPECT AND PROSPECT. 1978, 34, 1731. TETRAHEDRON A REVIEW.a
  170634. GABRIEL WEATHERHEAD
  170635. 10742
  170636. 11751N
  170637. 2/28/96V
  170638. SCHONBERG, A.; SINGER, E. CHEMISTRY OF NINHYDRIN AND OTHER CYCLIC 1,2,3 TRICARBONYL COMPOUNDS (IN GERMAN). 1978, 34, 1285. TETRAHEDRON A REVIEW.a
  170639. GABRIEL WEATHERHEAD
  170640. 10743
  170641. 11752N
  170642. 2/28/96VVCLIVE, D. L. J. MODERN ORGANOSELENIUM CHEMISTRY. 1978, 34, 1049. TETRAHEDRON A REVIEW.a
  170643. GABRIEL WEATHERHEAD
  170644. 10744
  170645. 11753N
  170646. 2/28/96V
  170647. SCHMIDT, A. H.; REID, W. THE PREPARATIVE CHEMISTRY OF CYCLOBUTENDIONE; III. SQUARIC (QUADRATIC) ACID, BENZOCYCLOBUTENONE AND THEIR DERIVATIVES (IN GERMAN). 1978, 869. SYNTHESIS A REVIEW.a
  170648. GABRIEL WEATHERHEAD
  170649. 10745
  170650. 11754N
  170651. 2/28/96VLSHARMA, S. THIOPHOSGENE IN ORGANIC SYNTHESIS. 1978, 803. SYNTHESIS A REVIEW.a
  170652. GABRIEL WEATHERHEAD
  170653. 10746
  170654. 11755N
  170655. 2/28/96
  170656. OPPOLZER, W. INTRAMOLECULAR CYCLOADDITION REACTIONS OF ORTHO QUINODIMETHANES IN ORGANIC SYNTHESIS. 1978, 793. SYNTHESIS A REVIEW.a
  170657. GABRIEL WEATHERHEAD
  170658. 10747
  170659. 11756N
  170660. 2/28/96VlFIELD, L. SOME DEVELOPMENTS IN SYNTHETIC ORGANIC SULFUR CHEMISTRY SINCE 1970. 1978, 713. SYNTHESIS A REVIEW.a
  170661. GABRIEL WEATHERHEAD
  170662. 10748
  170663. 11757N
  170664. 2/28/96V
  170665. KNORR, H., REID, W. THE PREPARATIVE CHEMISTRY OF CYCLOBUTENDIONE; II. REACTIONS OF ALKYL , ALKENYL  AND ARYLCYCLOBUTENDIONES (IN GERMAN). 1978, 649. SYNTHESIS A REVIEW.a
  170666. GABRIEL WEATHERHEAD
  170667. 10749
  170668. 11758N
  170669. 2/28/96V
  170670. BAIOCCHI, CORSI, G.; PALAZZO, G. SYNTHESIS, PROPERTIES, AND REACTIONS OF LH LNDAZOL 3 OLS AND 1,2 DIHYDRO 3H INDAZOL 3 ONES. 1978, 633. SYNTHESIS A REVIEW.a
  170671. GABRIEL WEATHERHEAD
  170672. 10750
  170673. 11759N
  170674. 2/28/96V{MAJORAL, J. P. SYNTHESIS AND REACTIONS OF HETEROCYCLIC COMPOUNDS CONTAINING A P N N LINKAGE. 1978, 557. SYNTHESIS A REVIEW.a
  170675. GABRIEL WEATHERHEAD
  170676. 10751
  170677. 11760
  170678. 2/28/96VJLENZ, G. R. THE PHOTOCHEMISTRY OF ENAMIDES. 1978, 489. SYNTHESIS A REVIEW.a
  170679. GABRIEL WEATHERHEAD
  170680. 10752
  170681. 11761N
  170682. 2/28/96V
  170683. KOCHETKOVA, N. S., KRYNKINA, YU. K. PRACTICAL APPLICATIONS OF CYCLOPENTADIENYL COMPLEXES OF TRANSITION METALS. 1978, 47, 486. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170684. GABRIEL WEATHERHEAD
  170685. 10753
  170686. 11762N
  170687. 2/28/96V
  170688. EGENBURG, I. Z. THE METHODS OF SYNTHESIS AND PROPERTIES OF CONJUGATED ENALLENIC HYDROCARBONS. 1978, 47, 470. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170689. GABRIEL WEATHERHEAD
  170690. 10754
  170691. 11763N
  170692. 2/28/96V
  170693. PROSTAKOV, N. S.; GAIVORONSKAYA, L. A. GAMMA PIPERIDINONES IN ORGANIC SYNTHESIS. 1978, 47, 447. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170694. GABRIEL WEATHERHEAD
  170695. 10755
  170696. 11764N
  170697. 2/28/96VuZARAISKII, A. P. THE STRUCTURAL FACTORS AND REACTIVITY OF BIPHENYL. 1978, 47, 440. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170698. GABRIEL WEATHERHEAD
  170699. 10756
  170700. 11765N
  170701. 2/28/96
  170702. yVuSOLOV'YANOV, A. A.; BELETSKAYA, I. P. THE REACTIVITY OF CARBANIONS. 1978, 47, 425. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170703. GABRIEL WEATHERHEAD
  170704. 10757
  170705. 11766N
  170706. 2/28/96VkLITVINENKO, L. M.; OLEINIK, N. M. BIFUNCTIONAL CATALYSIS. 1978, 47, 401. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170707. GABRIEL WEATHERHEAD
  170708. 10758
  170709. 11767N
  170710. 2/28/96V
  170711. ARKHIPOVA, I. A.; ZHUBANOV, B. A.; RAFIKOV, S. R. NEW HETEROCHAIN POLYMERS BASED ON CYCLIC IMIDES OF CARBOXYLIC ACID. 1978, 47, 368. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170712. GABRIEL WEATHERHEAD
  170713. 10759
  170714. 11768N
  170715. 2/28/96V
  170716. YASHINA, O. G., VERESHCHAGIN, L. I. NATURAL AND SYNTHETIC ACETYLENIC ANTIMYCOTICS. 1978, 47, 307. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170717. GABRIEL WEATHERHEAD
  170718. 10760
  170719. 11769N
  170720. 2/28/96V
  170721. GELLER, B. A. THE MECHANISM OF THE ELIMINATION OF AMMONIA IN THE CONDENSATION OF PRIMARY AMINO COMPOUNDS AND CERTAIN SYNTHESES OF NITROGEN CONTAINING HETEROCYCLES. 1978, 47, 297. RUSSIAN CHEMICAL REVIEWS A REVIEW.
  170722. GABRIEL WEATHERHEAD
  170723. 10761
  170724. 11770N
  170725. 2/28/96V
  170726. SERGEEV, N. M.; SUBBOTIN, O. A. 13C NMR SPECTROSCOPY OF SUBSTITUTED CYCLOHEXANES. 1978, 47, 265. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170727. GABRIEL WEATHERHEAD
  170728. 10762
  170729. 11771N
  170730. 2/28/96V
  170731. PLOTNIKOV, V. G.; OVCHINNIKOV. A. A. THE PHOTOCHEMICAL AND RADIATION CHEMICAL STABILITY OF MOLECULES. UNIMOLECULAR REACTIONS INVOLVING THE ABSTRACTION OF A HYDROGEN ATOM. 1978, 47, 247. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170732. GABRIEL WEATHERHEAD
  170733. 10763
  170734. 11772N
  170735. 2/28/96V{SADOVNIKOVA, M. S.; BELIKOV, V. M. INDUSTRIAL APPLICATIONS OF AMINO ACIDS. 1978 47, 199. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170736. GABRIEL WEATHERHEAD
  170737. 10764
  170738. 11773N
  170739. 2/28/96V
  170740. SOKOLOV, N. A.; ALEKSANDROV, YU A. ORGANIC PEROXIDES OF ALKALI METALS (ALKALI SALTS OF HYDROPEROXIDES). 1978, 47, 172. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170741. GABRIEL WEATHERHEAD
  170742. 10765
  170743. 11774N
  170744. 2/28/96
  170745. ZEFIROV, N. S.; KOZ'MIN, A. S.; ABRAMENKOV, A. V. THE PROBLEM OF TETRAHEDRANE. 1978, 47,163. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170746. GABRIEL WEATHERHEAD
  170747. 10766
  170748. 11775N
  170749. 2/28/96V{TODRES, Z. V. THE ROLE OF ONE ELECTRON TRANSFER IN SUBSTITUTION REACTIONS. 1978, 47,148. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170750. GABRIEL WEATHERHEAD
  170751. 10767
  170752. 11776N
  170753. 2/28/96V
  170754. ALESKEROV, M. A.; YUFIT, S. S., KUCHEROV, V. F. THE MECHANISM OF THE BETA EIIMINATION REACTION. 1978, 47,134. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170755. GABRIEL WEATHERHEAD
  170756. 10768
  170757. 11777N
  170758. 2/28/96V
  170759. KHUDYAKOV, I. V.; KUZ'MIN, V. A. OXIDATION REDUCTION REACTIONS OF FREE RADICALS. 1978, 47, 22. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170760. GABRIEL WEATHERHEAD
  170761. 10769
  170762. 11778N
  170763. 2/28/96V
  170764. KOROL', A. N. GAS CHROMATOGRAPHIC ANALYSIS OF PRODUCTS OF THE DECOMPOSITION OF PROTEINS AND NUCLEIC ACIDS. 1977, 46, 1202. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170765. GABRIEL WEATHERHEAD
  170766. 10770
  170767. 11779
  170768. 2/28/96V
  170769. SHELUDYAKOV, V. D.; MIRONOV, V. F. ORGANOSILICON CARBONATES AND CHLOROCARBONATES. 1977, 46,1167. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170770. GABRIEL WEATHERHEAD
  170771. 10771
  170772. 11780N
  170773. 2/28/96V
  170774. MAKOSZA, M. REACTIONS OF CARBANIONS AND HALOGENOCARBONS IN TWO PHASE SYSTEMS. 1977, 46, 151. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  170775. GABRIEL WEATHERHEAD
  170776. 10772
  170777. 11781N
  170778. 2/28/96V
  170779. SCAIANO, J. C.; LISSI, E. A., ENCINA, M. V. CHEMISTRY OF THE BIRADICALS PRODUCED IN THE NORRISH TYPE II REACTION. 1978, 2, 139. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  170780. GABRIEL WEATHERHEAD
  170781. 10773
  170782. 11782N
  170783. 2/28/96V
  170784. WHITTEN, D. G. PHOTOCHEMISTRY OF PORPHYRINS AND THEIR METAL COMPLEXES IN SOLUTION AND ORGANIZED MEDIA. 1978, 2,107. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  170785. GABRIEL WEATHERHEAD
  170786. 10774
  170787. 11783N
  170788. 2/28/96
  170789. CLAUDEL, B.; BREYSSE, M.; FAURE, L.; GUENIN, M. CHEMILUMINESCENCE AS A MEANS OF REVEALING INTERMEDIATE STAGES IN ADSORPTION AND CATALYSIS. 1978, 2, 75. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  170790. GABRIEL WEATHERHEAD
  170791. 10775
  170792. 11784N
  170793. 2/28/96V
  170794. ARTHUR, N. L.; BELL, T. N. AN EVALUATION OF THE KINETIC DATA FOR HYDROGEN ABSTRACTION FROM SILANES IN THE GAS PHASE. 1978, 2, 37. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  170795. GABRIEL WEATHERHEAD
  170796. 10776
  170797. 11785N
  170798. 2/28/96V
  170799. JACOX, M. E. STABILIZATION AND SPECTRA OF FREE RADICALS AND MOLECULAR IONS IN RARE GAS MATRICES. 1978, 2, 1. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  170800. GABRIEL WEATHERHEAD
  170801. 10777
  170802. 11786N
  170803. 2/28/96VpDAVIES, D. B. CONFORMATIONS OF NUCLEOSIDES AND NUCLEOTIDES. 1978,12, 135. PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  170804. GABRIEL WEATHERHEAD
  170805. 10778
  170806. 11787N
  170807. 2/28/96
  170808. OHIOFF, G. RECENT DEVELOPMENTS IN THE FIELD OF NATURALLY OCCURRING AROMA COMPONENTS. 1978, 35, 431. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  170809. GABRIEL WEATHERHEAD
  170810. 10779
  170811. 11788N
  170812. 2/28/96V
  170813. MURRAY, R. D. H. NATURALLY OCCURRING PLANT COUMARINS. 1978, 35, 199. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  170814. GABRIEL WEATHERHEAD
  170815. 10780
  170816. 11789N
  170817. 2/28/96V
  170818. PATTENDEN, G. NATURAL 4 YLIDENEBUTENOLIDES AND 4 YLIDENETETRONIC ACIDS. 1378, 35, 133. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  170819. GABRIEL WEATHERHEAD
  170820. 10781
  170821. 11790N
  170822. 2/28/96V
  170823. HERRMANN, V. K. HYDROXYCINNAMIC ACID AND HYDROXYBENZOIC ACID CONTAINING NATURAL PRODUCTS IN PLANTS (IN GERMAN). 1978, 35, 73. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  170824. GABRIEL WEATHERHEAD
  170825. 10782
  170826. 11791N
  170827. 2/28/96VhGOTTLIEB, O. R. NEOLIGNANS. 1978, 35, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.
  170828. GABRIEL WEATHERHEAD
  170829. 10783
  170830. 11792N
  170831. 2/28/96V
  170832. SOOS, Z. G. ELECTRONIC STRUCTURE OF ORGANIC CONDUCTORS AND SEMICONDUCTORS, 1978, 55, 546. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  170833. GABRIEL WEATHERHEAD
  170834. 10784
  170835. 11793N
  170836. 2/28/96V
  170837. ZUPAN, M., SKET, B. PHOTOCHEMISTRY OF FLUOROSUBSTITUTED AROMATIC AND HETEROAROMATIC MOLECULES. 1978,17, 92. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170838. GABRIEL WEATHERHEAD
  170839. 10785
  170840. 11794N
  170841. 2/28/96VuHUDLICKY, M. INTRAMOLECULAR NUCLEOPHILIC DISPLACEMENT OF FLUORINE. 1978,17, 80. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170842. GABRIEL WEATHERHEAD
  170843. 10786
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  170845. 2/28/96VrFILLER, R. REACTIONS OF ORGANIC COMPOUNDS WITH XENON FLUORIDES. 1978,17, 71. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170846. GABRIEL WEATHERHEAD
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  170848. 11796N
  170849. 2/28/96V
  170850. HESSE, R. H. APPLICATION OF FLUOROXY COMPOUNDS TO ORGANIC SYNTHESIS: ELECTROPHILIC FLUORINATION OF UNSATURATED MOLECULES. 1978,17, 60. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.
  170851. GABRIEL WEATHERHEAD
  170852. 10788
  170853. 11797N
  170854. 2/28/96V
  170855. KOLLONITSCH, J. NOVEL METHODS FOR SELECTIVE FLUORINATION OF ORGANIC COMPOUNDS: DESIGN AND SYNTHESIS OF FLUORINATED ANTIMETABOLITES. 1978,17, 53. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170856. GABRIEL WEATHERHEAD
  170857. 10789
  170858. 11798N
  170859. 2/28/96V
  170860. SCHACK, C. J.; CHRISTE, K. O. REACTIONS OF ELECTROPOSITIVE CHLORINE COMPOUNDS WITH FLUOROCARBONS. 1978,17, 20, ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170861. GABRIEL WEATHERHEAD
  170862. 10790
  170863. 11799N
  170864. 2/28/96V
  170865. SHREEVE, J. M. TRI  AND TETRACOORDINATE FLUOROSULFUR(IV) AND PENTACOORDINATE FLUOROSULFUR(VI) COMPOUNDS. 1978, ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170866. GABRIEL WEATHERHEAD
  170867. 10791
  170868. 11800N
  170869. 2/28/96V
  170870. ADOLF, W.; HECKER, E. DITERPENOID IRRITANTS AND COCARCINOGENS IN EUPHORBIACEAE AND THYMELAEACEAE: STRUCTURAL RELATIONSHIPS IN VIEW OF THEIR BIOGENESIS. 1977,16, 75. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170871. GABRIEL WEATHERHEAD
  170872. 10792
  170873. 11801N
  170874. 2/28/96
  170875. MACLEAN, D. B. SYNTHESIS AND BIOSYNTHESIS OF SPIROBENZYLISOQUINOLINE ALKALOIDS. 1977,16, 68. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170876. GABRIEL WEATHERHEAD
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  170878. 11802N
  170879. 2/28/96V
  170880. GOTTLIEB, H. E. TECHNIQUES FOR SIGNAL ASSIGNMENT IN 13C NMR SPECTROSCOPY OF NATURALLY OCCURRING AROMATIC COMPOUNDS. 1977,16, 57. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170881. GABRIEL WEATHERHEAD
  170882. 10794
  170883. 11803N
  170884. 2/28/96VzSCHEUER, P. J. THE VARIED AND FASCINATING CHEMISTRY OF MARINE MOLLUSKS. 1977,16, 52. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170885. GABRIEL WEATHERHEAD
  170886. 10795
  170887. 11804N
  170888. 2/28/96V
  170889. GOTTLIEB, O. R. THE FLAVONOIDS: INDISPENSABLE ADDITIONS TO A RECENT COVERAGE. 1977,16, 45. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170890. GABRIEL WEATHERHEAD
  170891. 10796
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  170893. 2/28/96VrHERZ, W. BIOGENETIC ASPECTS OF SESQUITERPENE LACTONE CHEMISTRY, 1977,16, 32. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  170894. GABRIEL WEATHERHEAD
  170895. 10797
  170896. 11806N
  170897. 2/28/96
  170898. V^ROMANCHICK, W. A.; JOULLIE, M. M. 1,2,4 TRIAZINOINDOLES. 1978, 9, 1631. HETEROCYCLES A REVIEW.a
  170899. GABRIEL WEATHERHEAD
  170900. 10798
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  170902. 2/28/96VyKHAN, M. A., FERREIRA DA ROCHA J. PYRROLOQUINOLINES IV. 3H PYRROLO[2,3 C]QUINOLINES. 1978, 9,1617. HETEROCYCLES A REVIEW.a
  170903. GABRIEL WEATHERHEAD
  170904. 10799
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  170906. 2/28/96VjUNGEMACH, F.; COOK, J. M. THE SPIROINDOLENINE INTERMEDIATE, A REVIEW. 1978, 9,1089. HETEROCYCLES A REVIEW.a
  170907. GABRIEL WEATHERHEAD
  170908. 10800
  170909. 11809N
  170910. 2/28/96VxKHAN, M. A.; FERREIRA DA ROCHA, J. PYRROLOQUINOLINES III. PYRROLO[3,4 B]QUINOLINES. 1978, 9,1059. HETEROCYCLES A REVIEW.a
  170911. GABRIEL WEATHERHEAD
  170912. 10801
  170913. 11810N
  170914. 2/28/96V\BICK, I. R. C.; SINCHAI, W. ALKALOIDS OF THE LAURACEAE. 1978, 9, 903. HETEROCYCLES A REVIEW.a
  170915. GABRIEL WEATHERHEAD
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  170917. 11811N
  170918. 2/28/96VCHADDADIN, M. J. ISOBENZOFURAN. 1978, 9. 865. HETEROCYCLES A REVIEW.a
  170919. GABRIEL WEATHERHEAD
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  170921. 11812N
  170922. 2/28/96
  170923. VaRAMSDEN, C. A. SEMIEMPIRICAL MO FOR ORGANIC CHEMISTS 1978,14, 396. CHEMISTRY IN BRITAIN A REVIEW.a
  170924. GABRIEL WEATHERHEAD
  170925. 10804
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  170927. 2/28/96V^HODGE, P. POLYMER SUPPORTS IN ORGANIC SYNTHESIS, 1978, 14, 237. CHEMISTRY IN BRITAIN A REVIEW.a
  170928. GABRIEL WEATHERHEAD
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  170931. 2/28/96VYTATLOW, J. C. ASPECTS OF ORGANOFLUORINE CHEMISTRY, 1978, CHEMISTRY AND INDUSTRY A REVIEW.a
  170932. GABRIEL WEATHERHEAD
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  170935. 2/28/96VcVAUGHAN, K.; STEVENS, M. F. G. MONOALKYLTRIAZENES. 1978, 7, 377. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170936. GABRIEL WEATHERHEAD
  170937. 10807
  170938. 11816N
  170939. 2/28/96VoMCNAB, H. MELDRUM'S ACID (2,2 DIMETHYL 1,3 DIOXANE 4,6 DIONE). 1978, 7, 345. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170940. GABRIEL WEATHERHEAD
  170941. 10808
  170942. 11817N
  170943. 2/28/96
  170944. BOELINS, H.; VAN DER LINDE, L. M.; DE RIJKE, D.; DE VALOIS P. J.; VAN DORT, J. M.; TAKKEN, H. J. MOLECULAR STRUCTURE AND ORGANOLEPTIC QUALITY. 1978, 7,167. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  170945. GABRIEL WEATHERHEAD
  170946. 10809
  170947. 11818N
  170948. 2/28/96VoREICHEN, W. OXYGEN , NITROGEN , AND SULFUR SUBSTITUTED HETEROALLENES. 1978, 78, 569. CHEMICAL REVIEWS A REVIEW.a
  170949. GABRIEL WEATHERHEAD
  170950. 10810
  170951. 11819N
  170952. 2/28/96VcSTIRLING, C. J. M. NUCLEOPHILIC ELIMINATIVE RING FISSION. 1978, 78, 517. CHEMICAL REVIEWS A REVIEW.a
  170953. GABRIEL WEATHERHEAD
  170954. 10811
  170955. 11820N
  170956. 2/28/96V{JONES, P. R.; DESIO, P. J. THE LESS FAMILIAR REACTIONS OF ORGANOCADMIUM REAGENTS. 1978, 78, 491. CHEMICAL REVIEWS A REVIEW.a
  170957. GABRIEL WEATHERHEAD
  170958. 10812
  170959. 11821N
  170960. 2/28/96VqASANO, T.; LE NOBLE, W. J. ACTIVATION AND REACTION VOLUMES IN SOLUTION. 1978, 78, 407. CHEMICAL REVIEWS A REVIEW.a
  170961. GABRIEL WEATHERHEAD
  170962. 10813
  170963. 11822N
  170964. 2/28/96
  170965. VLSTANG, P. J. UNSATURATED CARBENES. 1978, 78, 383. CHEMICAL REVIEWS A REVIEW.a
  170966. GABRIEL WEATHERHEAD
  170967. 10814
  170968. 11823N
  170969. 2/28/96VrTROST, B. M. ALPHA SULFENYLATED CARBONYL COMPOUNDS IN ORGANIC SYNTHESIS. 1978, 78, 363. CHEMICAL REVIEWS A REVIEW.a
  170970. GABRIEL WEATHERHEAD
  170971. 10815
  170972. 11824N
  170973. 2/28/96VyFU, P. P.; HARVEY, R. G. DEHYDROGENATION OF POLYCYCLIC HYDROAROMATIC COMPOUNDS. 1978, 78, 317. CHEMICAL REVIEWS A REVIEW.a
  170974. GABRIEL WEATHERHEAD
  170975. 10816
  170976. 11825N
  170977. 2/28/96V
  170978. OLAH, G. A.; PARKER, D. G.; YONEDA, N. SUPERACID CATALYZED OXYGENATION OF ALKANES. 1978,17, 909. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170979. GABRIEL WEATHERHEAD
  170980. 10817
  170981. 11826N
  170982. 2/28/96V
  170983. DEUCHERT, K.; HUNIG, S. MULTISTAGE ORGANIC REDOX SYSTEMS. A GENERAL STRUCTURAL PRINCIPLE. 1978,17, 875. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170984. GABRIEL WEATHERHEAD
  170985. 10818
  170986. 11827N
  170987. 2/28/96
  170988. HERRMANN, W. A. ORGANOMETALLIC SYNTHESES WITH DIAZOALKANES. 1978, 17, 800. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170989. GABRIEL WEATHERHEAD
  170990. 10819
  170991. 11828N
  170992. 2/28/96VxMANECKE, G.; STORCK, W. POLYMERIC CNTALYSTS. 1978,17, 657. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170993. GABRIEL WEATHERHEAD
  170994. 10820
  170995. 11829N
  170996. 2/28/96V
  170997. HOLLER, E. PROTEIN BIOSYNTHESIS: THE CODON SPECIFIC ACTIVATION OF AMINO ACIDS. 1978,17, 648. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  170998. GABRIEL WEATHERHEAD
  170999. 10821
  171000. 11830N
  171001. 2/28/96V
  171002. GRISEBACH, H., EBEL, J. PHYTOALEXINS CHEMICAL DEFENSE SUBSTANCES OF HIGHER PLANTS? 1978, 17, 635. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171003. GABRIEL WEATHERHEAD
  171004. 10822
  171005. 11831N
  171006. 2/28/96V
  171007. RIESS, J. G. LE BLANC, M. PERFLUORO COMPOUNDS AS BLOOD SUBSTITUTES. 1978, 17, 621. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171008. GABRIEL WEATHERHEAD
  171009. 10823
  171010. 11832N
  171011. 2/28/96V}SCHNEIDER, E. HISTIDINE IN ENZYME ACTIVE CENTERS. 1978 17, 583. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171012. GABRIEL WEATHERHEAD
  171013. 10824
  171014. 11833N
  171015. 2/28/96V
  171016. HOFLE, G.; STEGLICH, W., VORBRUGGEN, H. 4 DIALKYLAMINOPYRIDINES AS HIGHLY ACTIVE ACYLATION CATALYSTS. 1978,17, 569. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171017. GABRIEL WEATHERHEAD
  171018. 10825
  171019. 11834N
  171020. 2/28/96VsDURR, H.; GLEITER, R. SPIROCONJUGATION, 1978,17, 559. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171021. GABRIEL WEATHERHEAD
  171022. 10826
  171023. 11835N
  171024. 2/28/96V
  171025. BONNEMANN, H. COBALT CATALYZED PYRIDINE SYNTHESES FROM ALKYNES AND NITRILES. 1978,17, 505. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171026. GABRIEL WEATHERHEAD
  171027. 10827
  171028. 11836N
  171029. 2/28/96V
  171030. POSNER, G. H. ORGANIC REACTIONS AT ALUMINA SURFACES. 1978, 17, 487. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.
  171031. GABRIEL WEATHERHEAD
  171032. 10828
  171033. 11837N
  171034. 2/28/96V
  171035. OPPOLZER, W.; SNIECKUS V. INTRAMOLECULAR ENE REACTIONS IN ORGANIC SYNTHESIS. 1978, 17, 476. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171036. GABRIEL WEATHERHEAD
  171037. 10829
  171038. 11838N
  171039. 2/28/96VaBLOCK, E. ORGANIC SULFUR COMPOUNDS IN ORGANIC SYNTHESIS. 1978,11, 51. ALDRICHIMICA ACTA A REVIEW.a
  171040. GABRIEL WEATHERHEAD
  171041. 10830
  171042. 11839N
  171043. 2/28/96VbCLIVE, D. L. J. SELENIUM REAGENTS FOR ORGANIC SYNTHESIS. 1978, 11, 43. ALDRICHIMICA ACTA A REVIEW.a
  171044. GABRIEL WEATHERHEAD
  171045. 10831
  171046. 11840N
  171047. 2/28/96V^MASAMUNE, S. RECENT PROGRESS IN MACROLIDE SYNTHESIS. 1978, 11, 23. ALDRICHIMICA ACTA A REVIEW.a
  171048. GABRIEL WEATHERHEAD
  171049. 10832
  171050. 11841N
  171051. 2/28/96VnNEWAZ, S. S. RECENT METHODS FOR THE SYNTHESIS OF CONJUGATED LACTONES. 1977,10, 64. ALDRICHIMICA ACTA A REVIEW.a
  171052. GABRIEL WEATHERHEAD
  171053. 10833
  171054. 11842N
  171055. 2/28/96
  171056. VXYAKHOT, V.; ET AL. WHAT'S NEW IN EXCIMERS? 1978,11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171057. GABRIEL WEATHERHEAD
  171058. 10834
  171059. 11843N
  171060. 2/28/96V
  171061. ATKINSON R., ET AL. KINETICS AND MECHANISMS OF THE REACTIONS OF THE HYDROXYL RADICAL WITH ORGANIC COMPOUNDS IN THE GAS PHASE. 1978,11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171062. GABRIEL WEATHERHEAD
  171063. 10835
  171064. 11844N
  171065. 2/28/96V
  171066. JACOBS, H. J.; HAVINGA, E. PHOTOCHEMISTRY OF VITAMIN D AND ITS ISOMERS AND OF SIMPLE TRIENES. 1978,11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171067. GABRIEL WEATHERHEAD
  171068. 10836
  171069. 11845N
  171070. 2/28/96VqBEAVAN, S. W.; ET AL. PHOTOLUMINESCENCE METHODS IN POLYMER SCIENCE. 1978,11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171071. GABRIEL WEATHERHEAD
  171072. 10837
  171073. 11846N
  171074. 2/28/96ViBELLUS, D. PHYSICAL QUENCHERS OF SINGLET MOLECULAR OXYGEN. 1978, 11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171075. GABRIEL WEATHERHEAD
  171076. 10838
  171077. 11847N
  171078. 2/28/96
  171079. VeDELZENNE, G. A. ORGANIC PHOTOCHEMICAL IMAGING SYSTEMS. 1978, 11. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  171080. GABRIEL WEATHERHEAD
  171081. 10839
  171082. 11848N
  171083. 2/28/96V|DEY, P. M. BIOCHEMISTRY OF PLANT GALACTOMANNANS. 1978 35, 341. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171084. GABRIEL WEATHERHEAD
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  171086. 11849N
  171087. 2/28/96V
  171088. GOLDSTEIN, I. J.; HAYES, C. E. THE LECTINS: CARBOHYDRATE BINDING PROTEINS OF PLANTS AND ANIMALS. 1978, 35, ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171089. GABRIEL WEATHERHEAD
  171090. 10841
  171091. 11850N
  171092. 2/28/96V
  171093. GRISEBACH, H. BIOSYNTHESIS OF SUGAR COMPONENTS OF ANTIBIOTIC SUBSTANCES. 1978, 35, 81. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171094. GABRIEL WEATHERHEAD
  171095. 10842
  171096. 11851N
  171097. 2/28/96VrFERRIER, R. J. CARBOHYDRATE BORONATES. 1978, 35, 31. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171098. GABRIEL WEATHERHEAD
  171099. 10843
  171100. 11852N
  171101. 2/28/96
  171102. ALLERHAND, A. NATURAL ABUNDANCE CARBON 13 NMR SPECTROSCOPY OF PROTEINS. OBSERVATION AND USES OF NONPROTONATED AROMATIC CARBON RESONANCES. 1978,11, 469. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171103. GABRIEL WEATHERHEAD
  171104. 10844
  171105. 11853N
  171106. 2/28/96V
  171107. VAN DER PLAS, H. C. THE SN(ANRORC) MECHANISM: A NEW MECHANISM FOR NUCLEOPHILIC SUBSTITUTION. 1978,11, 462. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171108. GABRIEL WEATHERHEAD
  171109. 10845
  171110. 11854N
  171111. 2/28/96V{TROST, B. M. SOME ASPECTS OF ORGANOSULFUR MEDIATED SYNTHETIC METHODS, 1978,11, 453. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171112. GABRIEL WEATHERHEAD
  171113. 10846
  171114. 11855N
  171115. 2/28/96V
  171116. BERSON, J. A. THE CHEMISTRY OF TRIMETHYLENEMETHANES A NEW CLASS OF BIRADICAL REACTIVE INTERMEDIATES. 1978,11, 446. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171117. GABRIEL WEATHERHEAD
  171118. 10847
  171119. 11856N
  171120. 2/28/96VqBUNNETT, J. F. AROMATIC SUBSTITUTION BY THE SRN1 MECHANISM. 1978,11, 413. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.
  171121. GABRIEL WEATHERHEAD
  171122. 10848
  171123. 11857N
  171124. 2/28/96V
  171125. KANAOKA, Y. PHOTOREACTIONS OF CYCLIC IMIDES. EXAMPLES OF SYNTHETIC ORGANIC PHOTOCHEMISTRY. 1978,11, 407. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171126. GABRIEL WEATHERHEAD
  171127. 10849
  171128. 11858N
  171129. 2/28/96V
  171130. SKELL, P. S.; DAY, J. C. GROUND STATE AND EXCITED STATE CHEMISTRY OF SUCCINIMIDOYL RADICAL AND ITS CONGENERS. 1978, 11, 381. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171131. GABRIEL WEATHERHEAD
  171132. 10850
  171133. 11859N
  171134. 2/28/96V
  171135. MEYERS, A. I. ASYMMETRIC CARBON CARBON BOND FORMATION FROM CHIRAL OXAZOLINES. 1978, 11, 375. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171136. GABRIEL WEATHERHEAD
  171137. 10851
  171138. 11860N
  171139. 2/28/96VsKOZIAR, J. C., COWAN, D. 0. PHOTOCHEMICAL HEAVY ATOM EFFECTS. 1978,11, 334. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171140. GABRIEL WEATHERHEAD
  171141. 10852
  171142. 11861N
  171143. 2/28/96
  171144. LEZNOFF, C. G. THE USE OF INSOLUBLE POLYMER SUPPORTS IN GENERAL ORGANIC SYNTHESIS. 1978,11, 327. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171145. GABRIEL WEATHERHEAD
  171146. 10853
  171147. 11862N
  171148. 2/28/96V
  171149. POULTER, C. D.; RILLING, H. C. THE PRENYL TRANSFER REACTION. ENZYMATIC AND MECHANISTIC STUDIES OF THE 1' 4 COUPLING REACTION IN THE TERPENE BIOSYNTHETIC PATHWAY. 1978,11, 307. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171150. GABRIEL WEATHERHEAD
  171151. 10854
  171152. 11863N
  171153. 2/28/96V
  171154. MAITLIS, P. M. (PENTAMETHYLCYCLOPENTADIENYL)RHODIUM AND  IRIDIUM COMPLEXES: APPROACHES TO NEW TYPES OF HOMOGENEOUS CATALYSTS. 1 1978, 11, 301 . ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171155. GABRIEL WEATHERHEAD
  171156. 10855
  171157. 11864N
  171158. 2/28/96V
  171159. KESSAR, S. V. A NOVEL ROUTE TO CONDENSED POLYNUCLEAR SYSTEMS, REALITY AND ILLUSION OF BENZYNE INTERMEDIACY. I978, 11, 283. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171160. GABRIEL WEATHERHEAD
  171161. 10856
  171162. 11865N
  171163. 2/28/96
  171164. FYFE, C. A.; COCIVERA, M.; DAMJI, S. W. H. FLOW AND STOPPED FLOW NMR INVESTIGATIONS OF INTERMEDIATES IN CHEMICAL REACTIONS. 1978,11, 277. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171165. GABRIEL WEATHERHEAD
  171166. 10857
  171167. 11866N
  171168. 2/28/96V
  171169. STEWART, R.; SRINIVASAN, R. PROTON ACTIVATING FACTORS IN GENERAL ACID AND GENERAL BASE CATALYSIS. 1978,11, 271. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171170. GABRIEL WEATHERHEAD
  171171. 10858
  171172. 11867N
  171173. 2/28/96V
  171174. ZOLLER, U. THREE MEMBERED RINGS CONTAINING SULFUR SMALL RING HETEROCYCLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 42, PART 1, A. HASSNER, ED.), WILEY INTERSCIENCE: NEW YORK, 1983. A REVIEW.a
  171175. GABRIEL WEATHERHEAD
  171176. 10859
  171177. 11868N
  171178. 2/28/96V
  171179. NAIR, V. AZIRINES SMALL RING HETEROCYCLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 42, PART 1, A. HASSNER, ED.), WILEY INTERSCIENCE: NEW YORK, 1983. A REVIEW.a
  171180. GABRIEL WEATHERHEAD
  171181. 10860
  171182. 11869N
  171183. 2/28/96
  171184. DEYRUP, J. A. AZIRIDINES SMALL RING HETEROCYCLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 42, PART 1, A. HASSNER, ED.), WILEY INTERSCIENCE: NEW YORK, 1983. A REVIEW.a
  171185. GABRIEL WEATHERHEAD
  171186. 10861
  171187. 11870N
  171188. 2/28/96V
  171189. TURCHI, I. J. OXAZOLE CHEMISTRY. A REVIEW OF RECENT ADVANCES. 1981, 20, 32. INDUSTRIAL AND ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT A REVIEW.a
  171190. GABRIEL WEATHERHEAD
  171191. 10862
  171192. 11871N
  171193. 2/28/96VaTURCHI, I. J.; DEWAR, M. J. S. THE CHEMISTRY OF OXAZOLES 1975, 75, 389 CHEMICAL REVIEWS A REVIEW.a
  171194. GABRIEL WEATHERHEAD
  171195. 10863
  171196. 11872N
  171197. 2/28/96V
  171198. MARYANOFF, B. E. OXAZOLES AND OXAZOLINES IN ORGANIC SYNTHESIS, P 963. OXAZOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 45, I. J. TURCHI, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. A REVIEW.a
  171199. GABRIEL WEATHERHEAD
  171200. 10864
  171201. 11873N
  171202. 2/28/96
  171203. GINGRICH, H. L.; BAUM, J. S. MESOIONIC OXAZOLES, P 731. OXAZOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 45, I. J. TURCHI, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. A REVIEW.a
  171204. GABRIEL WEATHERHEAD
  171205. 10865
  171206. 11874N
  171207. 2/28/96V
  171208. RAO, Y. S.; FILLER, R. OXAZOLONES, P 361. OXAZOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 45, I. J. TURCHI, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. A REVIEW.a
  171209. GABRIEL WEATHERHEAD
  171210. 10866
  171211. 11875N
  171212. 2/28/96V
  171213. MARYANOFF, C. A. SPECTROSCOPIC PROPERTIES OF OXAZOLES, P 343. OXAZOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 45, I. J. TURCHI, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. A REVIEW.a
  171214. GABRIEL WEATHERHEAD
  171215. 10867
  171216. 11876N
  171217. 2/28/96V
  171218. TURCHI, I. J. OXAZOLES, P 1 OXAZOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 45, I. J. TURCHI, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. A REVIEW.a
  171219. GABRIEL WEATHERHEAD
  171220. 10868
  171221. 11877N
  171222. 2/28/96
  171223. V]STOWELL, J. C. CARBANIONS IN ORGANIC SYNTHESIS; WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171224. GABRIEL WEATHERHEAD
  171225. 10869
  171226. 11878N
  171227. 2/28/96V{SHAMMA, M.; HINDENLANG, D. M. CARBON NMR SHIFT ASSIGNMENTS OF AMINES AND ALKALOIDS; PLENUM PRESS: NEW YORK, 1979. A REVIEW.a
  171228. GABRIEL WEATHERHEAD
  171229. 10870
  171230. 11879N
  171231. 2/28/96VkREMERS, W. A. THE CHEMISTRY OF ANTITUMOR ANTIBIOTICS, VOL. 1; WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171232. GABRIEL WEATHERHEAD
  171233. 10871
  171234. 11880N
  171235. 2/28/96V
  171236. REICHARDT, CHR. SOLVENT EFFECTS IN ORGANIC CHEMISTRY: MONOGRAPHS IN MODERN CHEMISTRY VOL. 3; VERLAG CHEMIE: NEW YORK, 1979. A REVIEW.a
  171237. GABRIEL WEATHERHEAD
  171238. 10872
  171239. 11881N
  171240. 2/28/96VwPATAI, S., ED. CHEMISTRY OF THE CARBON CARBON TRIPLE BOND, PARTS 1 AND 2; WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171241. GABRIEL WEATHERHEAD
  171242. 10873
  171243. 11882N
  171244. 2/28/96
  171245. VnNONHEBEL, D. C., TEDDER, J. M., WALTON, J. C. RADICALS  CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, 1979. A REVIEW.a
  171246. GABRIEL WEATHERHEAD
  171247. 10874
  171248. 11883N
  171249. 2/28/96V
  171250. METZGER, J. V. THIAZOLE AND ITS DERIVATIVES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS SERIES, VOL. 34, PARTS 1, 2, AND 3); WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171251. GABRIEL WEATHERHEAD
  171252. 10875
  171253. 11884N
  171254. 2/28/96VxLEVY, G. C.; LICHTER, R. L. NITROGEN 15 NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; WILEY INTERSCIENCE: NEW YORK. A REVIEW.a
  171255. GABRIEL WEATHERHEAD
  171256. 10876
  171257. 11885N
  171258. 2/28/96VXKOCHI, J. K. ORGANIC MECHANISMS AND CATALYSIS; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  171259. GABRIEL WEATHERHEAD
  171260. 10877
  171261. 11886N
  171262. 2/28/96VlHOUGHTON, R. P. METAL COMPLEXES IN ORGANIC CHEMISTRY, CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, 1979. A REVIEW.a
  171263. GABRIEL WEATHERHEAD
  171264. 10878
  171265. 11887N
  171266. 2/28/96
  171267. HANSCH, C.; LEO, A. SUBSTITUENT CONSTANTS FOR CORRELATION  ANALYSIS IN CHEMISTRY AND BIOLOGY; WILEY  INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171268. GABRIEL WEATHERHEAD
  171269. 10879
  171270. 11888N
  171271. 2/28/96V
  171272. ENGELHARDT, H. (TRANSLATED FROM GERMAN BY G. GUT  NIKOV). HIGH PERFORMANCE LIQUID CHROMATOGRAPHY  SPRINGER VERLAG: NEW YORK, 1979. A REVIEW.a
  171273. GABRIEL WEATHERHEAD
  171274. 10880
  171275. 11889N
  171276. 2/28/96V|DUNITZ, J. D. X RAY ANALYSIS AND THE STRUCTURE OF ORGANIC MOLECULES; CORNELL UNIVERSITY PRESS: ITHACA, N.Y., 1979. A REVIEW.a
  171277. GABRIEL WEATHERHEAD
  171278. 10881
  171279. 11890N
  171280. 2/28/96VoDOLPHIN, D., ED. THE PORPHYRINS, VOL. IV, CHEMICAL CHEMISTRY, PART B; ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  171281. GABRIEL WEATHERHEAD
  171282. 10882
  171283. 11891N
  171284. 2/28/96VpDOLPHIN, D., ED. THE PORPHYRINS, VOL. III, PHYSICAL CHEMISTRY, PART A; ACADEMIC PRESS: NEW YORK, 1978. A REVIEW.a
  171285. GABRIEL WEATHERHEAD
  171286. 10883
  171287. 11892N
  171288. 2/28/96
  171289. DALTON, D. R. THE ALKALOIDS: THE FUNDAMENTAL CHEMISTRY
  171290. A BIOGENETIC APPROACH (STUDIES IN ORGANIC CHEMISTRY SERIES, VOL. 7); MARCEL DEKKER: NEW YORK, 1979. A REVIEW.a
  171291. GABRIEL WEATHERHEAD
  171292. 10884
  171293. 11893N
  171294. 2/28/96VpDALE, J. STEREOCHEMISTRY AND CONFORMATIONAL ANALYSIS VERLAG CHEMIE INTERNATIONAL INC.: NEW YORK, 1978. A REVIEW.a
  171295. GABRIEL WEATHERHEAD
  171296. 10885
  171297. 11894N
  171298. 2/28/96V
  171299. CHEESEMAN, G. W. H.; COOKSON, R. F., EDS. CONDENSED PYRAZINE (CHEMISTRY OF HETEROCYCLIC COMPOUNDS SERIES VOL. 35); WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171300. GABRIEL WEATHERHEAD
  171301. 10886
  171302. 11895N
  171303. 2/28/96VbCHARNEY, E. THE MOLECULAR BASIS OF OPTICAL ACTIVITY; WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171304. GABRIEL WEATHERHEAD
  171305. 10887
  171306. 11896N
  171307. 2/28/96VqBROWN, G. H.; WOLKEN, J. J. LIQUID CRYSTALS AND BIOLOGICAL  STRUCTURES; ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  171308. GABRIEL WEATHERHEAD
  171309. 10888
  171310. 11897N
  171311. 2/28/96
  171312. VwBOHME, H.; VIEHE, H. G., EDS. IMINIUM SALTS IN ORGANIC CHEMISTRY, PART 2; WILEY INTERSCIENCE: NEW YORK, 1979. A REVIEW.a
  171313. GABRIEL WEATHERHEAD
  171314. 10889
  171315. 11898N
  171316. 2/28/96V
  171317. PAQUETTE, L. A. THE DEVELOPMENT OF POLYQUINANE CHEMISTRY. 1979, 79, 41. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  171318. GABRIEL WEATHERHEAD
  171319. 10890
  171320. 11899N
  171321. 2/28/96V
  171322. HOUK, K. N. THEORETICAL AND EXPERIMENTAL INSIGHTS INTO CYCLOADDITION REACTIONS. 1979, 79,1. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  171323. GABRIEL WEATHERHEAD
  171324. 10891
  171325. 11900N
  171326. 2/28/96V
  171327. KRINSKY, N. I. BIOLOGICAL ROLES OF SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171328. GABRIEL WEATHERHEAD
  171329. 10892
  171330. 11901N
  171331. 2/28/96
  171332. KAPLAN, M. L.; TROZZOLO, A. M. ROLE OF SINGLET OXYGEN IN THE DEGRADATION OF POLYMERS. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171333. GABRIEL WEATHERHEAD
  171334. 10893
  171335. 11902N
  171336. 2/28/96V
  171337. SAITO, I.; MATSUURA, T. THE OXIDATIONS OF ELECTRON RICH AROMATIC COMPOUNDS. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171338. GABRIEL WEATHERHEAD
  171339. 10894
  171340. 11903N
  171341. 2/28/96V
  171342. WASSERMAN, H. W.; LIPSHUTZ, B. H. REACTIONS OF SINGLET OXYGEN WITH HETEROCYCLIC SYSTEMS. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171343. GABRIEL WEATHERHEAD
  171344. 10895
  171345. JACSCIRADOM DIAZO KETONE WOLFF REARRANGEMENT OXIRENE KETO CARBENE REVIEW THEORYM
  171346. 11904N
  171347. 2/28/96V8THE WOLFF REARRANGEMENT.  OXIRENE
  171348. KETENE INTERCONVERSIONW
  171349. VOL 116 1994 P 10159a
  171350. GABRIEL WEATHERHEAD
  171351. 10896
  171352. 11905N
  171353. 2/28/96
  171354. BARTLETT, P. D.; LANDIS, M. E. THE 1,2 DIOXETANES. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171355. GABRIEL WEATHERHEAD
  171356. 10897
  171357. 11906N
  171358. 2/28/96V
  171359. SCHAAP, A. P.; ZAKLIKA, K. A. 1,2 CYCLOADDITION REACTIONS OF SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171360. GABRIEL WEATHERHEAD
  171361. 10898
  171362. 11907N
  171363. 2/28/96V
  171364. FOOTE, C. S. QUENCHING OF SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171365. GABRIEL WEATHERHEAD
  171366. 10899
  171367. 11908N
  171368. 2/28/96V
  171369. KEARNS, D. R. SOLVENT AND SOLVENT ISOTOPE EFFECTS ON THE LIFETIME OF SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171370. GABRIEL WEATHERHEAD
  171371. 10900
  171372. 11909N
  171373. 2/28/96
  171374. MURRAY, R. W. CHEMICAL SOURCES OF SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171375. GABRIEL WEATHERHEAD
  171376. 10901
  171377. 11910N
  171378. 2/28/96V
  171379. OGRYZLO, E. A. GASEOUS SINGLET OXYGEN. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171380. GABRIEL WEATHERHEAD
  171381. 10902
  171382. 11911N
  171383. 2/28/96V
  171384. KASHA, M.; BRABHAM, D. E. SINGLET OXYGEN ELECTRONIC STRUCTURE AND PHOTOSENSITIZATION. SINGLET OXYGEN (H. H. WASSERMAN AND R. W. MURRAY, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171385. GABRIEL WEATHERHEAD
  171386. 10903
  171387. 11912N
  171388. 2/28/96V
  171389. SIMS, J. J., ROSE, A. F.; IZAC R. R. APPLICATIONS OF 13C NMR TO MARINE NATURAL PROLUCTS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES (VOL. 2, P. J. SCHEUER, ED.), ACADEMIC PRESS: NEW YORK, 1978 A REVIEW.a
  171390. GABRIEL WEATHERHEAD
  171391. 10904
  171392. 11913N
  171393. 2/28/96
  171394. TURSCH, B.; BRAEKMAN, J. C.; DALOZE, D.; KAISIN, M. TERPENOIDS FROM COELENTERATES. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES (VOL. 2, P. J. SCHEUER, ED.), ACADEMIC PRESS: NEW YORK, 1978 A REVIEW.a
  171395. GABRIEL WEATHERHEAD
  171396. 10905
  171397. 11914N
  171398. 2/28/96V
  171399. FENICAL, W. DITERPENOIDS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES (VOL. 2, P. J. SCHEUER, ED.), ACADEMIC PRESS: NEW YORK, 1978 A REVIEW.a
  171400. GABRIEL WEATHERHEAD
  171401. 10906
  171402. 11915N
  171403. 2/28/96V
  171404. GOAD, L. J. THE STEROLS OF MARINE INVERTEBRATES: COMPOSITION, BIOSYNTHESIS, AND METABOLITES. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES (VOL. 2, P. J. SCHEUER, ED.), ACADEMIC PRESS: NEW YORK, 1978 A REVIEW.a
  171405. GABRIEL WEATHERHEAD
  171406. 10907
  171407. 11916N
  171408. 2/28/96V
  171409. LIAAEN JENSEN, S. MARINE CAROTENOIDS. MARINE NATURAL PRODUCTS, CHEMICAL AND BIOLOGICAL PERSPECTIVES (VOL. 2, P. J. SCHEUER, ED.), ACADEMIC PRESS: NEW YORK, 1978 A REVIEW.a
  171410. GABRIEL WEATHERHEAD
  171411. 10908
  171412. 11917N
  171413. 2/28/96V
  171414. REMERS, W. A. INDOLE ALDEHYDES AND KETONES, P 357. CHEMISTRY OF INDOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 25, PART 3, W. J. HOULIHAN, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  171415. GABRIEL WEATHERHEAD
  171416. 10909
  171417. 11918N
  171418. 2/28/96V
  171419. SPANDE T. F. HYDROXYINDOLES, INDOLE ALCOHOLS, AND INDOLETHIOLS, P 1. CHEMISTRY OF INDOLES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 25, PART 3, W. J. HOULIHAN, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  171420. GABRIEL WEATHERHEAD
  171421. 10910
  171422. 11919N
  171423. 2/28/96V
  171424. BESTMANN, H. J.; ZIMMERMANN, R. ALKYLATIONS AND ACYLATIONS OF PHOSPHONIUM YLIDES. CARBON CARBON BOND FORMATION (TECHNIQUES AND APPLICATIONS IN ORGANIC SYNTHESIS SERIES, VOL. 1, R. L. AUGUSTINE, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  171425. GABRIEL WEATHERHEAD
  171426. 10911
  171427. 11920N
  171428. 2/28/96
  171429. CAINE, D. ALKYLATION AND RELATED REACTIONS OF KETONES AND ALDEHYDES VIA METAL ENOLATES. CARBON CARBON BOND FORMATION (TECHNIQUES AND APPLICATIONS IN ORGANIC SYNTHESIS SERIES, VOL. 1, R. L. AUGUSTINE, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  171430. GABRIEL WEATHERHEAD
  171431. 10912
  171432. 11921N
  171433. 2/28/96V
  171434. HAJOS, Z. G. ALDOL AND RELATED REACTIONS. CARBON CARBON BOND FORMATION (TECHNIQUES AND APPLICATIONS IN ORGANIC SYNTHESIS SERIES, VOL. 1, R. L. AUGUSTINE, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  171435. GABRIEL WEATHERHEAD
  171436. 10913
  171437. 11922N
  171438. 2/28/96V
  171439. NEGISHI, E I. SELECTIVE CARBON CARBON BOND FORMATION UIA TRANSITION METAL CATALYSIS: IS NICKEL OR PALLADIUM BETTER THAN COPPER ?, P 285. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171440. GABRIEL WEATHERHEAD
  171441. 10914
  171442. 11923N
  171443. 2/28/96
  171444. LAROCK, R. C. NEW APPLICATIONS OF ORGANOMERCURY,  PALLADIUM, AND  RHODIUM COMPOUNDS IN ORGANIC SYNTHESIS, P 251. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171445. GABRIEL WEATHERHEAD
  171446. 10915
  171447. 11924N
  171448. 2/28/96V
  171449. ZWEIFEL, G. THE VERSATILE ALKENYLALANES AND ALKENYLBORANES, P 229. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171450. GABRIEL WEATHERHEAD
  171451. 10916
  171452. 11925N
  171453. 2/28/96V
  171454. MIDLAND, M. M. ASYMMETRIC SYNTHESIS VIA BORANES: CHIRAL ALLENIC BORANES AND TRIALKYLBORANE REDUCING AGENTS, P 207. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171455. GABRIEL WEATHERHEAD
  171456. 10917
  171457. 11926N
  171458. 2/28/96V
  171459. KABALKA, G. W. RADIONUCLIDE INCORPORATION VIA ORGANOBORANES, P 199. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.
  171460. GABRIEL WEATHERHEAD
  171461. 10918
  171462. 11927N
  171463. 2/28/96V
  171464. LANE, C. F. SELECTIVE REDUCTIONS USING METAL HYDRIDES, P 181. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171465. GABRIEL WEATHERHEAD
  171466. 10919
  171467. 11928N
  171468. 2/28/96
  171469. CHAMBERS, R. L.; JENSEN, F. R. STEREOCHEMISTRY OF THE SE2 BROMINE CLEAVAGE OF TETRAALKYLTIN COMPOUNDS IN CARBON TETRACHLORIDE AND METHANOL SOLVENTS, P 169. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.
  171470. GABRIEL WEATHERHEAD
  171471. 10920
  171472. 11929N
  171473. 2/28/96
  171474. aROGIC, M. M.; DEMMIN, T. R. COPPER(II) INDUCED OXYGENOLYSIS OF O BENZOQUINONES, CATECHOLS, AND PHENOLS: THE ACTIVE COPPER(II) SPECIES, ROLE OF CUPRIC CHLORIDE AND THE GENERAL QUESTION OF ACTIVATION OF MOLECULAR OXYGEN BY DIOXYGENASES, P 141. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.
  171475. GABRIEL WEATHERHEAD
  171476. 10921
  171477. 11930N
  171478. 2/28/96V
  171479. BANK, S. EFFECTS OF STERIC STRAIN ON THE PREPARATION, STABILITY, AND REACTIONS OF ARYL ANIONS AND AMINES, P 109. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171480. GABRIEL WEATHERHEAD
  171481. 10922
  171482. 11931N
  171483. 2/28/96V
  171484. RUSSELL, G. A. MOLECULAR AND CONFORMATIONAL EQUILIBRIA STUDIED BY ELECTRON SPIN RESONANCE SPECTROSCOPY, P 59. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171485. GABRIEL WEATHERHEAD
  171486. 10923
  171487. 11932N
  171488. 2/28/96V
  171489. STOCK, L. M.; WASIELEWSKI, M. R. CHARGE AND SPIN DELOCALIZATION TO THE TRIFLUOROMETHYL GROUP, P 41. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171490. GABRIEL WEATHERHEAD
  171491. 10924
  171492. 11933N
  171493. 2/28/96
  171494. PETERS, E. N.; RAVINDRANATHAN, M.; BROWN, H. C. THE MECHANISTIC PROBE OF INCREASING ELECTRON DEMAND IN THE STUDY OF SOLVOLYTIC REACTIONS, P 1. ASPECTS OF MECHANISM AND ORGANOMETALLIC CHEMISTRY (J. H. BREWSTER, ED.), PLENUM PRESS: NEW YORK, 1978 A REVIEW.a
  171495. GABRIEL WEATHERHEAD
  171496. 10925
  171497. 11934N
  171498. 2/28/96V
  171499. KAPIL, R. S.; BROWN, R. T. MONOTERPENE ALKALOID GLYCOSIDES. THE ALKALOIDS (VOL. 17, R. H. F. MANSKE AND R. RODRIGO, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171500. GABRIEL WEATHERHEAD
  171501. 10926
  171502. 11935N
  171503. 2/28/96V
  171504. SANTAVY, F. PAPAVERACEAE ALKALOIDS, II. THE ALKALOIDS (VOL. 17, R. H. F. MANSKE AND R. RODRIGO, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171505. GABRIEL WEATHERHEAD
  171506. 10927
  171507. 11936N
  171508. 2/28/96V
  171509. CORDELL, G. A. THE ASPIDOSPERMA ALKALOIDS. THE ALKALOIDS (VOL. 17, R. H. F. MANSKE AND R. RODRIGO, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171510. GABRIEL WEATHERHEAD
  171511. 10928
  171512. 11937N
  171513. 2/28/96
  171514. GRUNDON, M. E. QUINOLINE ALKALOIDS RELATED TO ANTHRANILIC ACID. THE ALKALOIDS (VOL. 17, R. H. F. MANSKE AND R. RODRIGO, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171515. GABRIEL WEATHERHEAD
  171516. 10929
  171517. 11938N
  171518. 2/28/96V
  171519. PELLETIER, S. W.; MODY, N. V. THE STRUCTURE AND SYNTHESIS OF C19 DITERPENOID ALKALOIDS. THE ALKALOIDS (VOL. 17, R. H. F. MANSKE AND R. RODRIGO, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  171520. GABRIEL WEATHERHEAD
  171521. 10930
  171522. 11939N
  171523. 2/28/96VcWRIGHT, D. E. THE ORTHOSOMYCINS, A NEW FAMILY OF ANTIBIOTICS. 1979, 35, 1207. TETRAHEDRON A REVIEW.a
  171524. GABRIEL WEATHERHEAD
  171525. 10931
  171526. 11940N
  171527. 2/28/96VbBROWN, E.; RAGAULT, M. THE SYNTHESES OF C NOR D HOMOSTEROIDS. 1979, 35, 911. TETRAHEDRON A REVIEW.a
  171528. GABRIEL WEATHERHEAD
  171529. 10932
  171530. 11941N
  171531. 2/28/96V]REBECK, JR., J. MECHANISTIC STUDIES USING SOLID SUPPOTS. 1979, 35, 723. TETRAHEDRON A REVIEW.a
  171532. GABRIEL WEATHERHEAD
  171533. 10933
  171534. 11942N
  171535. 2/28/96
  171536. *VgBROWN, H. C.; KRISHNAMURTHY, S. FORTY YEARS OF HYDRIDE REDUCTIONS. 1979, 35, 567. TETRAHEDRON A REVIEW.a
  171537. GABRIEL WEATHERHEAD
  171538. 10934
  171539. 11943N
  171540. 2/28/96V|WIGFIELD, D. C. STEREOCHEMISTRY AND MECHANISM OF KETONE REDUCTIONS BY HYDRIDE REAGENTS. 1979, 35, 449. TETRAHEDRON A REVIEW.a
  171541. GABRIEL WEATHERHEAD
  171542. 10935
  171543. 11944N
  171544. 2/28/96VkMCKILLOP, A., YOUNG, D. W. ORGANIC SYNTHESIS USING SUPPORTED REAGENTS
  171545. PART I. 1979, 40. SYNTHESIS A REVIEW.a
  171546. GABRIEL WEATHERHEAD
  171547. 10936
  171548. 11945N
  171549. 2/28/96VNPETERS,J.A. SYNTHESIS OF BICYCLO[3.3.1]NONANES. 1979, 321. SYNTHESIS A REVIEW.a
  171550. GABRIEL WEATHERHEAD
  171551. 10937
  171552. 11946N
  171553. 2/28/96V
  171554. LIEBSCHER,J. HARTMANN, H. 3 CHLORO 2 PROPENIMINIUM SALTS AS USEFUL SYNTHONS IN ORGANIC CHEMISTRY (IN GER.). 1979, 241. SYNTHESIS A REVIEW.a
  171555. GABRIEL WEATHERHEAD
  171556. 10938
  171557. 11947N
  171558. 2/28/96
  171559. BLAZEVIC, N.; KOLBAH, D.; BELIN, B.; SUNJIC, V.; KAJFEI, F. HEXAMETHYLENETETRAMINE, A VERSATILE REAGENT IN ORGANIC SYNTHESIS. 1979, 161. SYNTHESIS A REVIEW.a
  171560. GABRIEL WEATHERHEAD
  171561. 10939
  171562. 11948N
  171563. 2/28/96V
  171564. PUDOVIK, A. N.; KONOVALOVA, I. V. ADDITION REACTIONS OF ESTERS OF PHOSPHORUS(III) ACIDS WITH UNSATURATED SYSTEMS. 1979, 81. SYNTHESIS A REVIEW.a
  171565. GABRIEL WEATHERHEAD
  171566. 10940
  171567. 11949N
  171568. 2/28/96V
  171569. HO, T. L. REDUCTION OF ORGANIC COMPOUNDS WITH LOW VALENT SPECIES OF GROUP IVB, VB, AND VIB METALS. 1979, 1. SYNTHESIS A REVIEW.a
  171570. GABRIEL WEATHERHEAD
  171571. 10941
  171572. 11950N
  171573. 2/28/96V
  171574. SERGEEV, V. A., SHITIKOV, V. K.; NEDEL'KIN, V. I. POLY(ARYLENE SULPHIDES)
  171575. PREPARATION, STRUCTURE, AND PROPERTIES. 1978, 47, 1095. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171576. GABRIEL WEATHERHEAD
  171577. 10942
  171578. 11951N
  171579. 2/28/96
  171580. KOLDOBSKII, G. 1.; OSTROVSKII, V. A.; GIDASPOV, B. V.  SCHMIDT REACTION WITH ALDEHYDES AND CARBOXYLIC ACIDS. 1978, 47, 1084. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171581. GABRIEL WEATHERHEAD
  171582. 10943
  171583. 11952N
  171584. 2/28/96VlGITIS, S. S.; KAMINSKII, A. YA. JANOVSKY SIGMA COMPLEXES. 1978, 47, 1061. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171585. GABRIEL WEATHERHEAD
  171586. 10944
  171587. 11953N
  171588. 2/28/96V
  171589. POZHARSKII, A. F., SIMONOV, A. M.; DORON'KIN, V. N. ADVANCES IN THE STUDY OF THE CHICHIBABIN REACTION. 1978, 47, 1042. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171590. GABRIEL WEATHERHEAD
  171591. 10945
  171592. 11954N
  171593. 2/28/96V
  171594. MARTIN, D.; BAUER, M.; PANKRATOV, V. A. CYCLOTRIMERIZATION OF CYANO COMPOUNDS INTO 1,3,5 TRIAZINES. 1978, 47, 975. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171595. GABRIEL WEATHERHEAD
  171596. 10946
  171597. 11955N
  171598. 2/28/96V
  171599. ZAKHARKIN, L. I.; GUSEVA, V. V. THE CHEMISTRY OF 1,5,9 CYCLODODECATRIENE AND SYNTHESES BASED ON IT. 1978, 47, 955. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171600. GABRIEL WEATHERHEAD
  171601. 10947
  171602. 11956N
  171603. 2/28/96V
  171604. ISHMAEVA, E. A. THE POLARITY AND STRUCTURE OF UNSATURATED DERIVATIVES OF FOUR COORDINATED PHOSPHORUS. 1978, 47, 896. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171605. GABRIEL WEATHERHEAD
  171606. 10948
  171607. 11957N
  171608. 2/28/96V
  171609. LUTSENKO, I. F.; PROSKURNINA, M. V. ORGANIC PHOSPHORUS COMPOUNDS WITH A P P BOND. 1978, 47, 880. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171610. GABRIEL WEATHERHEAD
  171611. 10949
  171612. 11958N
  171613. 2/28/96V
  171614. GILYAROV, V. A. THE IMIDE AMINE AND IMIDE IMIDE REARRANGEMENTS OF IMIDOPHOSPHORUS COMPOUNDS. 1978, 47, 870. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171615. GABRIEL WEATHERHEAD
  171616. 10950
  171617. 11959N
  171618. 2/28/96V
  171619. NIFANT'EV, E. E. CHEMISTRY OF PHOSPHINYLIDENE COMPOUNDS
  171620. ADVANCES AND PROSPECTS OF DEVELOPMENT. 1978, 47, 835. RUSSIAN CHEMICAL REVIEWS 84a
  171621. GABRIEL WEATHERHEAD
  171622. 10951
  171623. 11960N
  171624. 2/28/96
  171625. KABACHNIK, M. I., MASTRYUKOVA, T. A., FEDIN, E. I. VAISBERG, M. S.; MOROZOV, L. L.; PETROVSKII, P. V.; SHIPOV, A. E. OPTICAL ISOMERS IN SOLUTION INVESTIGATED BY NUCLEAR MAGNETIC RESONANCE. 1978, 47, 821. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171626. GABRIEL WEATHERHEAD
  171627. 10952
  171628. 11961N
  171629. 2/28/96V
  171630. MICHALSKI, J., REIMSCHUSSEL, W., KAMINSKI, R. ORGANIC MONOTHIOPYROPHOSPHATES. 1978, 47, 814. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171631. GABRIEL WEATHERHEAD
  171632. 10953
  171633. 11962N
  171634. 2/28/96V
  171635. KHUSAINOVA, N. G., PUDOVIK, A. N. ORGANOPHOSPHORUS COMPOUNDS IN 1,3 DIPOLAR CYCLOADDITION. 1978, 47, 803. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171636. GABRIEL WEATHERHEAD
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  171638. 11963N
  171639. 2/28/96VrPOLUMBRIK, O. M. ADVANCES IN THE CHEMISTRY OF VERDAZYL RADICALS. 1978, 47, 767. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171640. GABRIEL WEATHERHEAD
  171641. 10955
  171642. 11964N
  171643. 2/28/96
  171644. FRIDLAND, S. V.; CHERNOKAL'SKII, B. D. THE STRUCTURE AND REACTIVITY OF PHOSPHORUS PENTACHLORIDE. 1978, 47, 742. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171645. GABRIEL WEATHERHEAD
  171646. 10956
  171647. 11965N
  171648. 2/28/96V
  171649. KOZHEVNIKOV, I. V.; MATVEEV, K. I. OXIDATIVE COUPLING OF AROMATIC SYSTEMS UNDER THE INFLUENCE OF TRANSITION METAL COMPOUNDS. 1978, 47, 649. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171650. GABRIEL WEATHERHEAD
  171651. 10957
  171652. 11966N
  171653. 2/28/96V
  171654. GREKOV, A. P., VESELOV V. YA. THE ALPHA EFFECT IN THE CHEMISTRY OF ORGANIC COMPOUNDS 1978, 47, 631. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  171655. GABRIEL WEATHERHEAD
  171656. 10958
  171657. 11967N
  171658. 2/28/96V
  171659. COLLIN, G. J. THE FATE OF EXCITED UNSATURATED RADICALS PRODUCED IN THE VACUUM UV PHOTOLYSIS OF GASEOUS OLEFINS. 1979, 2, 377. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171660. GABRIEL WEATHERHEAD
  171661. 10959
  171662. 11968N
  171663. 2/28/96VpCAPOZZI, G.; LUCCHINI, V.; MODENA, G. THIIRENIUM IONS. 1979, 2, 347. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.
  171664. GABRIEL WEATHERHEAD
  171665. 10960
  171666. 11969N
  171667. 2/28/96V
  171668. KIMURA, K. IONIC PHOTODISSOCIATION OF WEAK GROUND STATE ELECTRON DONOR ACCEPTOR COMPLEXES. 1979, 2, 321. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171669. GABRIEL WEATHERHEAD
  171670. 10961
  171671. 11970N
  171672. 2/28/96V
  171673. CSIZMADIA, I. G. THEORETICAL STUDIES ON POSITIVELY CHARGED MOLECULAR SPECIES. 1979, 2, 297. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171674. GABRIEL WEATHERHEAD
  171675. 10962
  171676. 11971N
  171677. 2/28/96V
  171678. FORD, P. C. LIGAND SUBSTITUENT EFFECTS IN TRANSITION METAL PHOTOCHEMISTRY
  171679. THE TUNING OF EXCITED STATES. 1979, 2, 267. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171680. GABRIEL WEATHERHEAD
  171681. 10963
  171682. 11972N
  171683. 2/28/96V
  171684. CORNELISSE, J., LODDER, G., HAVINGA, E. PATHWAYS AND INTERMEDIATES OF NUCLEOPHILIC AROMATIC PHOTOSUBSTITUTION REACTIONS. 1979, 2, 231. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171685. GABRIEL WEATHERHEAD
  171686. 10964
  171687. 11973N
  171688. 2/28/96
  171689. IVuTSUNASHIMA, S.; SATO, S. CADMIUM PHOTOSENSITIZED REACTIONS. 1979, 2, 201. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  171690. GABRIEL WEATHERHEAD
  171691. 10965
  171692. 11974N
  171693. 2/28/96V
  171694. WEINHEIMER, A. J.; CHANG, C. W. J.; MATSON, J. A. NATURALLY OCCURRING CEMBRANES. 1979, 36, 285. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  171695. GABRIEL WEATHERHEAD
  171696. 10966
  171697. 11975N
  171698. 2/28/96V
  171699. OHLOFF, G.; FLAMENT, 1. HETEROATOMIC SUBSTANCES IN AROMA COMPOUNDS. 1979, 36, 231. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  171700. GABRIEL WEATHERHEAD
  171701. 10967
  171702. 11976N
  171703. 2/28/96V
  171704. WEHRLI, F. W., NISHIDA, T. USE OF C 13 NMR IN NATURAL PRODUCTS CHEMISTRY. 1979, 36,1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  171705. GABRIEL WEATHERHEAD
  171706. 10968
  171707. 11977N
  171708. 2/28/96VwKRAUS, M., PATCHORNIK, A. POLYMERIC CARRIERS AS IMMOBILIZING MEDIA. 1978,17, 298. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  171709. GABRIEL WEATHERHEAD
  171710. 10969
  171711. 11978N
  171712. 2/28/96VlMORAWETZ, H. REACTIVITY OF SYSTEMS CONTAINING POLYMERS. 1978, 17, 287. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  171713. GABRIEL WEATHERHEAD
  171714. 10970
  171715. 11979N
  171716. 2/28/96V
  171717. VLIEGENTHART, J. F. G. ENZYMIC AND NON ENZYMIC OXIDATION OF POLYUNSATURATED FATTY ACIDS. 1979, 241. CHEMISTRY AND INDUSTRY A REVIEW.a
  171718. GABRIEL WEATHERHEAD
  171719. 10971
  171720. 11980N
  171721. 2/28/96V|ELLIOTT, M.; JANES, N. F. SYNTHETIC PYRETHROIDS
  171722. A NEW CLASS OF INSECTICIDE. 1978, 7, 473. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  171723. GABRIEL WEATHERHEAD
  171724. 10972
  171725. 11981N
  171726. 2/28/96VnLEMIEUX, R. U. HUMAN BLOOD GROUPS AND CARBOHYDRATE CHEMISTRY. 1978, 7, 423. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  171727. GABRIEL WEATHERHEAD
  171728. 10973
  171729. 11982N
  171730. 2/28/96V_FOX, M. A. THE PHOTOEXCITED STATES OF ORGANIC ANIONS. 1979, 79, 253. CHEMICAL REVIEWS A REVIEW.a
  171731. GABRIEL WEATHERHEAD
  171732. 10974
  171733. 11983N
  171734. 2/28/96
  171735. SV`TAYLOR, E. C.; TURCHI, I. J. 1,5 DIPOLAR CYCLIZATIONS. 1979, 79, 181. CHEMICAL REVIEWS A REVIEW.a
  171736. GABRIEL WEATHERHEAD
  171737. 10975
  171738. 11984N
  171739. 2/28/96V
  171740. BRADSHAW, J. S.; MAAS, G. E.; IZATT, R. M.; CHRISTENSEN, J. J. SYNTHETIC MACROCYCLIC DI  AND TETRAESTER COMPOUNDS. 1979, 79, 37. CHEMICAL REVIEWS A REVIEW.a
  171741. GABRIEL WEATHERHEAD
  171742. 10976
  171743. 11985N
  171744. 2/28/96V
  171745. BOWEN, R. D.; WILLIAMS, D. H.; SCHWARZ, H. THE CHEMISTRY OF ISOLATED CATIONS. 1979,18, 451. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171746. GABRIEL WEATHERHEAD
  171747. 10977
  171748. 11986N
  171749. 2/28/96V
  171750. WHITTEN, D. G. PHOTOCHEMICAL REACTIONS OF SURFACTANT MOLECULES IN CONDENSED MONOLAYER ASSEMBLIES
  171751.  ENVIRONMENTAL CONTROL AND MODIFICATION OF REACTIVITY. 1979, 18, 440. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171752. GABRIEL WEATHERHEAD
  171753. 10978
  171754. 11987N
  171755. 2/28/96
  171756. FRANCK, B. KEY BUILDING BLOCKS OF NATURAL PRODUCTS BIOSYNTHESIS AND THEIR SIGNIFICANCE IN CHEMISTRY AND MEDICINE.1979,18, 429. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171757. GABRIEL WEATHERHEAD
  171758. 10979
  171759. 11988N
  171760. 2/28/96VlREGEN, S. L. TRIPHASE CATALYSIS. 1979,18, 421. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171761. GABRIEL WEATHERHEAD
  171762. 10980
  171763. 11989N
  171764. 2/28/96V
  171765. METIU, H.; ROSS, J.; WHITESIDES, G. M. A BASIS FOR ORBITAL SYMMETRY RULES. 1979,18, 377. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171766. GABRIEL WEATHERHEAD
  171767. 10981
  171768. 11990N
  171769. 2/28/96V
  171770. BOTT, K. ALKENEDIAZONIUM SALTS: A NEW CHAPTER OF CLASSICAL ORGANIC CHEMISTRY. 1979,18, 259. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171771. GABRIEL WEATHERHEAD
  171772. 10982
  171773. 11991N
  171774. 2/28/96VuSEEBACH, D. METHODS OF REACTIVITY UMPOLUNG. 1979,18 239 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171775. GABRIEL WEATHERHEAD
  171776. 10983
  171777. 11992N
  171778. 2/28/96VkNAKAGAWA, M. ANNULENOANNULENES. 1979,18, 202. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171779. GABRIEL WEATHERHEAD
  171780. 10984
  171781. 11993N
  171782. 2/28/96V
  171783. REETZ, M. T. ANCHIMERICALLY ACCELERATED BOND HOMOLYSES. 1979,18, 173. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171784. GABRIEL WEATHERHEAD
  171785. 10985
  171786. 11994N
  171787. 2/28/96V
  171788. REICHARDT, CH. EMPIRICAL PARAMETERS OF SOLVENT POLARITY AS LINEAR FREE ENERGY RELATIONSHIPS. 1979,18, 98. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171789. GABRIEL WEATHERHEAD
  171790. 10986
  171791. 11995N
  171792. 2/28/96V
  171793. KAUFFMANN TH. THE PRINCIPLE OF ARENO ANALOGY HETEROCYCLOPOLYAROMATIC COMPOUNDS. 1979,18,1 ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  171794. GABRIEL WEATHERHEAD
  171795. 10987
  171796. 11996N
  171797. 2/28/96VDEVANS, C. A. SPIN TRAPPING. 1979,12, 23. ALDRICHIMICA ACTA A REVIEW.a
  171798. GABRIEL WEATHERHEAD
  171799. 10988
  171800. 11997N
  171801. 2/28/96
  171802. aViGLADYSZ, J. A. TRIALKYLBOROHYDRIDES IN ORGANOMETALLIC SYNTHESIS. 1979,12, 13. ALDRICHIMICA ACTA A REVIEW.a
  171803. GABRIEL WEATHERHEAD
  171804. 10989
  171805. 11998N
  171806. 2/28/96V|BROWN, H. C.; KRISHNAMURTHY, S. BORANES FOR ORGANIC REDUCTIONS
  171807. A FORTY YEAR ODYSSEY. 1979,12, 3. ALDRICHIMICA ACTA A REVIEW.a
  171808. GABRIEL WEATHERHEAD
  171809. 10990
  171810. 11999N
  171811. 2/28/96V
  171812. BERGER, S. NUCLEAR MAGNETIC RELAXATION: RECENT PROBLEMS AND PROGRESS. 1978,16, 239. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  171813. GABRIEL WEATHERHEAD
  171814. 10991
  171815. 12000N
  171816. 2/28/96VxWILLIAMS, J. O. ELECTRICAL CONDUCTION IN ORGANIC SOLIDS. 1978, 16, 159. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  171817. GABRIEL WEATHERHEAD
  171818. 10992
  171819. 12001N
  171820. 2/28/96VsALBERY, J.; KREEVOY, M. M. METHYL TRANSFER REACTIONS. 1978, 16, 87 ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  171821. GABRIEL WEATHERHEAD
  171822. 10993
  171823. 12002N
  171824. 2/28/96
  171825. TEDDER, J. M.; WALTON, J. C. DIRECTIVE EFFECTS IN GAS PHASE RADICAL ADDITIVE REACTIONS. 1978,16, 51. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  171826. GABRIEL WEATHERHEAD
  171827. 10994
  171828. 12003N
  171829. 2/28/96V
  171830. RIDD, J. H. DIFFUSION CONTROL AND PRE ASSOCIATION IN NITROSATION, NITRATION AND HALOGENATION. 1978,16,1. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  171831. GABRIEL WEATHERHEAD
  171832. 10995
  171833. 12004N
  171834. 2/28/96V}CALDERON, N.; LAWRENCE, J. P.; OFSTEAD, E. A. OLEFIN METATHESIS. 1978,17, 449. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171835. GABRIEL WEATHERHEAD
  171836. 10996
  171837. 12005N
  171838. 2/28/96V
  171839. SPEIER, J. L. HOMOGENEOUS CATALYSIS OF HYDROSILATION BY TRANSITION METALS. 1978,17, 407. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171840. GABRIEL WEATHERHEAD
  171841. 10997
  171842. 12006N
  171843. 2/28/96V
  171844. JAMES, B. R. HYDROGENATION REACTIONS CATALYZED BY TRANSITION METAL COMPLEXES. 1978,17, 319. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171845. GABRIEL WEATHERHEAD
  171846. 10998
  171847. 12007N
  171848. 2/28/96V}SU, A. C. L. CATALYTIC CODIMERIZATION OF ETHYLENE AND BUTADIENE. 1978,17, 269. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171849. GABRIEL WEATHERHEAD
  171850. 10999
  171851. 12008N
  171852. 2/28/96V
  171853. FORSTER, D. MECHANISTIC PATHWAYS IN THE CATALYTIC CARBONYLATION OF METHANOL BY RHODIUM AND IRIDIUM COMPLEXES. 1978,17, 255. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171854. GABRIEL WEATHERHEAD
  171855. 11000
  171856. 12009N
  171857. 2/28/96V
  171858. CHIUSOLI, G. P.; SALERNO, G. SYNTHETIC APPLICATION OF ORGANONICKEL COMPLEXES IN ORGANIC CHEMISTRY. 1978,17, ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171859. GABRIEL WEATHERHEAD
  171860. 11001
  171861. 12010N
  171862. 2/28/96V
  171863. TSUJI, J. PALLADIUM CATALYZED REACTIONS OF BUTADIENE AND ISOPRENE. 1978,1 7,141. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171864. GABRIEL WEATHERHEAD
  171865. 11002
  171866. 12011N
  171867. 2/28/96
  171868. BOGDANOVIC, B. SELECTIVITY CONTROL IN NICKEL CATALYZED OLEFIN OLIGOMERIZATION. 1978,17, 105. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171869. GABRIEL WEATHERHEAD
  171870. 11003
  171871. 12012N
  171872. 2/28/96VeMASTERS, C. THE FISCHER TROPSCH REACTION. 1978,17, 61. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171873. GABRIEL WEATHERHEAD
  171874. 11004
  171875. 12013N
  171876. 2/28/96VYPRUETT, R. L. HYDROFORMYLATION. 1978,17,1. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  171877. GABRIEL WEATHERHEAD
  171878. 11005
  171879. 12014N
  171880. 2/28/96V
  171881. ACHESON, R. M., ELMORE, N. F. REACTIONS OF ACETYLENECARBOXYLIC ESTERS WITH NITROGEN CONTAINING HETEROCYCLES. 1978, 23, 265. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  171882. GABRIEL WEATHERHEAD
  171883. 11006
  171884. 12015N
  171885. 2/28/96VyFLETCHER, I. J.; SIEGRIST, A. E. OLEFIN SYNTHESIS WITH ANILS. 1978, 23, 172. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  171886. GABRIEL WEATHERHEAD
  171887. 11007
  171888. 12016N
  171889. 2/28/96
  171890. SWINBOURNE, F. J.; HUNT, J. H.; KLINKERT, G. ADVANCES IN INDOLIZINE CHEMISTRY. 1978, 23,104. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  171891. GABRIEL WEATHERHEAD
  171892. 11008
  171893. 12017N
  171894. 2/28/96V
  171895. ANASTASSIOU, A. G.; KASMAI, H. S. MEDIUM LARGE AND LARGE PI EXCESSIVE HETEROANNULENES. 1978, 23, 55. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  171896. GABRIEL WEATHERHEAD
  171897. 11009
  171898. 12018N
  171899. 2/28/96VmECKSTEIN, Z.; URBANSKI, T. 1,3 0XAZINE DERIVATIVES. 1978, 23, 2. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  171900. GABRIEL WEATHERHEAD
  171901. 11010
  171902. 12019N
  171903. 2/28/96V
  171904. IKEHARA, M.; OHTSUKA, E.; MARKHAM, A. F. THE SYNTHESIS OF POLYNUCLEOTIDES. 1979, 36,135. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171905. GABRIEL WEATHERHEAD
  171906. 11011
  171907. 12020N
  171908. 2/28/96V
  171909. KEGLEVIC, D. GLYCOSIDURONIC ACIDS AND RELATED COMPOUNDS. 1979, 36, 57. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  171910. GABRIEL WEATHERHEAD
  171911. 11012
  171912. 12021N
  171913. 2/28/96
  171914. yV}GOREWITT, B.; TSUTSUI, M. SIGMA PI REARRANGEMENTS AND THEIR ROLE IN CATALYSIS. 1978, 27, 227. ADVANCES IN CATALYSIS A REVIEW.a
  171915. GABRIEL WEATHERHEAD
  171916. 11013
  171917. 12022N
  171918. 2/28/96V
  171919. KEULKS, G. W., KRENZKE, L. D., NOTERMANN, T. N. SELECTIVE OXIDATION OF PROPYLENE. 1978, 27,183. ADVANCES IN CATALYSIS A REVIEW.a
  171920. GABRIEL WEATHERHEAD
  171921. 11014
  171922. 12023N
  171923. 2/28/96VnECKSTEIN, F. PHOSPHOROTHIOATE ANALOGUES OF NUCLEOTIDES. 1979, 12, 204. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171924. GABRIEL WEATHERHEAD
  171925. 11015
  171926. 12024N
  171927. 2/28/96V
  171928. STIRLING, C. J. M. LEAVING GROUPS AND NUCLEOFUGALITY IN ELIMINATION AND OTHER ORGANIC REACTIONS. 1979,12,198. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171929. GABRIEL WEATHERHEAD
  171930. 11016
  171931. 12025N
  171932. 2/28/96V
  171933. GREEN, B. S.; LAHAV, M.; RABINOVICH, D. ASYMMETRIC SYNTHESIS VIA REACTIONS IN CHIRAL CRYSTALS. 1979,12,191. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171934. GABRIEL WEATHERHEAD
  171935. 11017
  171936. 12026N
  171937. 2/28/96
  171938. HANESSIAN, S. APPROACHES TO THE TOTAL SYNTHESIS OF NATURAL PRODUCTS USING CHIRAL TEMPLATES DERIVED FROM CARBOHYDRATES. 1979,12, 159. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171939. GABRIEL WEATHERHEAD
  171940. 11018
  171941. 12027N
  171942. 2/28/96VrLEWIS, F. D. FORMATION AND REACTIONS OF STILBENE EXCIPLEXES. 1979,12, 152. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171943. GABRIEL WEATHERHEAD
  171944. 11019
  171945. 12028N
  171946. 2/28/96V
  171947. HECK, R. F. PALLADIUM CATALYZED REACTIONS OF ORGANIC HALIDES WITH OLEFINS. 1979,12,146. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171948. GABRIEL WEATHERHEAD
  171949. 11020
  171950. 12029N
  171951. 2/28/96V_PIETRA, F. REVIVAL OF TROPONOID CHEMISTRY. 1979,12,132. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171952. GABRIEL WEATHERHEAD
  171953. 11021
  171954. 12030N
  171955. 2/28/96VVMOORE, H. W. ZWITTAZIDO CLEAVAGE. 1979,12,125. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171956. GABRIEL WEATHERHEAD
  171957. 11022
  171958. 12031N
  171959. 2/28/96
  171960. VaMENGER, F. M. ON THE STRUCTURE OF MICELLES. 1979,12, 111. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171961. GABRIEL WEATHERHEAD
  171962. 11023
  171963. 12032N
  171964. 2/28/96VqSCHROCK, R. R. ALKYLIDENE COMPLEXES OF NIOBIUM AND TANTALUM. 1979,12, 98. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171965. GABRIEL WEATHERHEAD
  171966. 11024
  171967. 12033N
  171968. 2/28/96V
  171969. HECT, S. S.; CHEN, C H. B., HOFFMANN, D. TOBACCO SPECIFIC NITROSAMINES: OCCURRENCE, FORMATION, CARCINOGENICITY, AND METABOLISM. 1979,12, 92. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171970. GABRIEL WEATHERHEAD
  171971. 11025
  171972. 12034N
  171973. 2/28/96V
  171974. TORRANCE, J. B. THE DIFFERENCE BETWEEN METALLIC AND INSULATING SALTS OF TETRACYANOQUINODIMETHANE (TCNQ): HOW TO DESIGN AN ORGANIC METAL. 1979,12, 79. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171975. GABRIEL WEATHERHEAD
  171976. 11026
  171977. 12035N
  171978. 2/28/96VvDANISHEFSKY, S. ELECTROPHILIC CYCLOPROPANES IN ORGANIC SYNTHESIS. 1979,12, 66. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171979. GABRIEL WEATHERHEAD
  171980. 11027
  171981. 12036N
  171982. 2/28/96V
  171983. YOYORI, R. ORGANIC SYNTHESIS VIA THE POLYBROMO KETONE IRON CARBONYL REACTION. 1979,12, 61. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171984. GABRIEL WEATHERHEAD
  171985. 11028
  171986. 12037N
  171987. 2/28/96V
  171988. BUNCEL, E.; WILSON, H. INITIAL STATE AND TRANSITION STATE SOLVENT EFFECTS ON REACTION RATES. 1979,12, 42. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171989. GABRIEL WEATHERHEAD
  171990. 11029
  171991. 12038N
  171992. 2/28/96V
  171993. DRENTH, W.; NOLTE, R. J. M. POLY(IMINOMETHYLENE): RIGID ROD HELICAL POLYMERS. 1979,12, 30. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171994. GABRIEL WEATHERHEAD
  171995. 11030
  171996. 12039N
  171997. 2/28/96V~REICH H. J. FUNCTIONAL GROUP MANIPULATION USING ORGANOSELENIUM REAGENTS. 1979, 12, 22. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  171998. GABRIEL WEATHERHEAD
  171999. 11031
  172000. 12040N
  172001. 2/28/96V
  172002. BATTERSBY, A. R.; MCDONALD E. THE TYPE III PROBLEM IN PORPHYRIN BIOSYNTHESIS. 1979,12,14. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172003. GABRIEL WEATHERHEAD
  172004. 11032
  172005. 12041N
  172006. 2/28/96
  172007. VuGOODMAN, M.; CHOREV, M. LINEAR MODIFIED RETRO PEPTIDE STRUCTURES. 1979,12, 1. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172008. GABRIEL WEATHERHEAD
  172009. 11033
  172010. 12042N
  172011. 2/28/96V~WISEMAN, P. AN INTRODUCTION TO INDUSTRIAL ORGANIC CHEMISTRY, 2ND ED. APPLIED SCIENCE PUBLISHERS LTD.: ENGLAND, 1979. A REVIEW.a
  172012. GABRIEL WEATHERHEAD
  172013. 11034
  172014. 12043N
  172015. 2/28/96VsSTANG, P. J.; RAPPOPORT, Z.; SUBRAMANIAN, L. R., HANACK M. VINYL CATIONS. ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  172016. GABRIEL WEATHERHEAD
  172017. 11035
  172018. 12044N
  172019. 2/28/96VgRYLANDER, P. N. CATALYTIC HYDROGENATION IN ORGANIC SYNTHESES. ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  172020. GABRIEL WEATHERHEAD
  172021. 11036
  172022. 12045N
  172023. 2/28/96VbNORMAN, R. O. C. PRINCIPLES OF ORGANIC SYNTHESIS, 2ND ED. HALSTED PRESS: NEW YORK, 1979. A REVIEW.a
  172024. GABRIEL WEATHERHEAD
  172025. 11037
  172026. 12046N
  172027. 2/28/96VjNEGISHI, E. I. ORGANOMETALLICS IN ORGANIC SYNTHESIS, VOL. 1. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.
  172028. GABRIEL WEATHERHEAD
  172029. 11038
  172030. 12047N
  172031. 2/28/96V
  172032. MUNDY, B. P. CONCEPTS OF ORGANIC SYNTHESIS. CARBOCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY SERIES, VOL. 8). MARCEL DEKKER: NEW YORK, 1979. A REVIEW.a
  172033. GABRIEL WEATHERHEAD
  172034. 11039
  172035. 12048N
  172036. 2/28/96V
  172037. MATHIEU, J.; WEILL RAYNAL, J. FORMATION OF C C BONDS (INTRODUCTION OF AN ALPHA FUNCTIONAL CARBON CHAIN, VOL. III). GEORG THIEME PUBLISHERS: STUTTGART, 1979. A REVIEW.a
  172038. GABRIEL WEATHERHEAD
  172039. 11040
  172040. 12049N
  172041. 2/28/96VxLEDNICER, D.; MITSCHER, L. A. ORGANIC CHEMISTRY OF DRUG SYNTHESIS, VOL. 2. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  172042. GABRIEL WEATHERHEAD
  172043. 11041
  172044. 12050N
  172045. 2/28/96VWHARMON, R. E., ED. ASYMMETRY IN CARBOHYDRATES. MARCEL DEKKER: NEW YORK, 1979. A REVIEW.a
  172046. GABRIEL WEATHERHEAD
  172047. 11042
  172048. 12051N
  172049. 2/28/96ViGEOFFROY, G. L., WRIGHTON, M. S. ORGANOMETALLIC PHOTOCHEMISTRY. ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  172050. GABRIEL WEATHERHEAD
  172051. 11043
  172052. 12052N
  172053. 2/28/96VdDRENTH, W., KWART, H. KINETICS APPLIED TO ORGANIC REACTIONS. MARCEL DEKKER: NEWYORK, 1980. A REVIEW.a
  172054. GABRIEL WEATHERHEAD
  172055. 11044
  172056. 12053N
  172057. 2/28/96VhDEGANELLO, G. TRANSITION METAL COMPLEXES OF CYCLIC POLYOLEFIN. ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  172058. GABRIEL WEATHERHEAD
  172059. 11045
  172060. 12054N
  172061. 2/28/96VgBRADLEY, D. C.; MEHROTRA, R. C.; GAUR, D. P. METAL ALKOXIDES. ACADEMIC PRESS: NEW YORK, 1979. A REVIEW.a
  172062. GABRIEL WEATHERHEAD
  172063. 11046
  172064. 12055N
  172065. 2/28/96VyBLACKBOROW J. R., YOUNG, D. METAL VAPOR SYNTHESIS IN ORGANOMETALIIC CHEMISTRY. SPRINGER VERLAG: NEW YORK, 1979. A REVIEW.a
  172066. GABRIEL WEATHERHEAD
  172067. 11047
  172068. 12056N
  172069. 2/28/96VpBERDY, J., ED. CRC HANDBOOK OF ANTIBIOTIC COMPOUNDS VOL. I, II, III, AND IV. CRC PRESS: FLORIDA, 1980. A REVIEW.a
  172070. GABRIEL WEATHERHEAD
  172071. 11048
  172072. 12057N
  172073. 2/28/96
  172074. VORONKOW, M. G. BIOLOGICAL ACTIVITY OF SILATRANES. 1979, 84, 77. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172075. GABRIEL WEATHERHEAD
  172076. 11049
  172077. 12058N
  172078. 2/28/96V
  172079. TACKE, R.; WANNAGAT, U. SYNTHESES AND PROPERTIES OF BIOACTIVE ORGANO SILICON COMPOUNDS. 1979, 84, 1. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172080. GABRIEL WEATHERHEAD
  172081. 11050
  172082. 12059N
  172083. 2/28/96V
  172084. REDEN, J.; DURCKHEIMER, W. AMINOGLYCOSIDE ANTIBIOTICS
  172085. CHEMISTRY, BIOCHEMISTRY STRUCTURE ACTIVITY RELATIONSHIPS. 1979, 83, 105. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172086. GABRIEL WEATHERHEAD
  172087. 11051
  172088. 12060N
  172089. 2/28/96V
  172090. ULLRICH, V. CYTOCHROME P450 AND BIOLOGICAL HYDROXYLATION REACTIONS. 1979, 83, 67. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172091. GABRIEL WEATHERHEAD
  172092. 11052
  172093. 12061N
  172094. 2/28/96
  172095. DELUCA, H. F.; PAAREN, H. E.; SCHNOES, H. K. VITAMIN D AND CALCIUM METABOLISM. 1979, 83,1. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172096. GABRIEL WEATHERHEAD
  172097. 11053
  172098. 12062N
  172099. 2/28/96V
  172100. KIRMSE, W. REARRANGEMENTS OF CARBOCATIONS. STEREOCHEMISTRY AND MECHANISM. 1979, 80,125. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172101. GABRIEL WEATHERHEAD
  172102. 11054
  172103. 12063N
  172104. 2/28/96V
  172105. HOGEVEEN, H.; VAN KRUCHTEN, E. M. G. A. WAGNER MEERWEIN REARRANGEMENTS IN LONG LIVED POLYMETHYL SUBSTITUTED BICYCLO[3.2.0]HEPTADIENYL CATIONS. 1979, 80, 89. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172106. GABRIEL WEATHERHEAD
  172107. 11055
  172108. 12064N
  172109. 2/28/96V
  172110. OLAH, G. A. FROM BORON TRIFLUORIDE TO ANTIMONY PENTAFLUORIDE IN SEARCH OF STABLE CARBOCATIONS. 1979, 80, 19. TOPICS IN CURRENT CHEMISTRY SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172111. GABRIEL WEATHERHEAD
  172112. 11056
  172113. 12065N
  172114. 2/28/96
  172115. BROWN, H. C. MEERWEIN AND EQUILIBRATING CARBOCATIONS. 1979,  80, 1. TOPICS IN CURRENT CHEMISTRY, SPRINGER VERLAG: NEW YORK, 1979 A REVIEW.a
  172116. GABRIEL WEATHERHEAD
  172117. 11057
  172118. 12066N
  172119. 2/28/96V
  172120. MONIZ, W. B.; PORANSKI, JR., C. F.; SOJKA, S. A. 13C CIDNP AS A MECHANISTIC AND KINETIC PROBE, P 362. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172121. GABRIEL WEATHERHEAD
  172122. 11058
  172123. 12067N
  172124. 2/28/96V
  172125. TORCHIA, D. A., VANDERHART, D. L. HIGH POWER DOUBLE RESONANCE STUDIES OF FIBROUS PROTEINS, PROTEOGLYCANS AND MODEL MEMBRANES, P 325. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172126. GABRIEL WEATHERHEAD
  172127. 11059
  172128. 12068N
  172129. 2/28/96V
  172130. SCHAEFER, J.; STEJSKAL, E. O. HIGH RESOLUTION 13C NMR OF SOLID POLYMERS, P 284. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172131. GABRIEL WEATHERHEAD
  172132. 11060
  172133. 12069N
  172134. 2/28/96V
  172135. ELIEL, E. L., PIETRUSIEWICZ, K. M. 13C NMR OF NONAROMATIC HETEROCYCLIC COMPOUNDS, P 172. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172136. GABRIEL WEATHERHEAD
  172137. 11061
  172138. 12070N
  172139. 2/28/96V
  172140. WRIGHT, D. A.; AXELSON, D. E.; LEVY, G. C. PHYSICAL CHEMICAL APPLICATIONS OF 13C SPIN RELAXATION MEASUREMENTS, P 104. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172141. GABRIEL WEATHERHEAD
  172142. 11062
  172143. 12071N
  172144. 2/28/96
  172145. $ANET, F. A. L., DALRYMPLE, D. L., GRANT, D. M., HILL, H. HOULT, D. I.; JOHNSON, L. F.; SHOOLERY, J. N.; TERPSTRA, D., ZENS, A. P. EXPERIMENTAL TECHNIQUES IN 13C NMR SPECTROSCOPY, P 2. TOPICS IN CARBON 13 NMR SPECTROSCOPY (VOL. 3, G. C. LEVY, ED.), WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.
  172146. GABRIEL WEATHERHEAD
  172147. 11063
  172148. 12072N
  172149. 2/28/96
  172150. WULFMAN, D. S.; POLING, B. METAL SALT CATALYZED CARBENOIDS. REACTIVE INTERMEDIATES (VOL. 1, R. A. ABRAMOVITCH, ED.), PLENUM PUBLISHING CORPORATION: NEW YORK, 1980 A REVIEW.a
  172151. GABRIEL WEATHERHEAD
  172152. 11064
  172153. 12073N
  172154. 2/28/96V
  172155. WENTRUP, C. THE BEHAVIOR OF ARYLCARBENES AND NITRENES IN THE GAS PHASE. REACTIVE INTERMEDIATES (VOL. 1, R. A. ABRAMOVITCH, ED.), PLENUM PUBLISHING CORPORATION: NEW YORK, 1980 A REVIEW.a
  172156. GABRIEL WEATHERHEAD
  172157. 11065
  172158. 12074N
  172159. 2/28/96V
  172160. CHOW, Y L. AMINIUM RADICALS. REACTIVE INTERMEDIATES (VOL. 1, R. A. ABRAMOVITCH, ED.), PLENUM PUBLISHING CORPORATION: NEW YORK, 1980 A REVIEW.a
  172161. GABRIEL WEATHERHEAD
  172162. 11066
  172163. 12075N
  172164. 2/28/96V
  172165. KLABUNDE K. J. METAL ATOMS AS REACTIVE INTERMEDIATES. REACTIVE INTERMEDIATES (VOL. 1, R. A. ABRAMOVITCH, ED.), PLENUM PUBLISHING CORPORATION: NEW YORK, 1980 A REVIEW.a
  172166. GABRIEL WEATHERHEAD
  172167. 11067
  172168. 12076N
  172169. 2/28/96
  172170. SHEVLIN, P. B. THE PREPARATION AND REACTIONS OF ATOMIC CARBON. REACTIVE INTERMEDIATES (VOL. 1, R. A. ABRAMOVITCH, ED.), PLENUM PUBLISHING CORPORATION: NEW YORK, 1980 A REVIEW.a
  172171. GABRIEL WEATHERHEAD
  172172. 11068
  172173. 12077N
  172174. 2/28/96V
  172175. LINDENBAUM, S.; RYTTING, J. H.; STERNSON, L. A. IONOPHORES
  172176. BIOLOGICAL TRANSPORT MEDIATORS, P 219. PROGRESS IN MACROCYCLIC CHEMISTRY (VOL. 1, R. M. IZATT AND J. J. CHRISTENSEN, ED.) WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172177. GABRIEL WEATHERHEAD
  172178. 11069
  172179. 12078N
  172180. 2/28/96
  172181. $REINHOUDT, D. N.; DE JONG, F. CROWN ETHERS AND RELATED MACROCYCLES WITH BIS(METHYLENE)AROMATIC OR  HETEROAROMATIC SUBUNITS: THEIR SYNTHESIS AND COMPLEXATION, P 157. PROGRESS IN MACROCYCLIC CHEMISTRY (VOL. 1, R. M. IZATT AND J. J. CHRISTENSEN, ED.) WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.
  172182. GABRIEL WEATHERHEAD
  172183. 11070
  172184. 12079N
  172185. 2/28/96
  172186. POONIA, N. S. MULTIDENTATE MACROMOLECULES: PRINCIPLES OF COMPLEXATION WITH ALKALI AND ALKALINE EARTH CATIONS P 115. PROGRESS IN MACROCYCLIC CHEMISTRY (VOL. 1, R. M. IZATT AND J. J. CHRISTENSEN, ED.) WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.a
  172187. GABRIEL WEATHERHEAD
  172188. 11071
  172189. 12080N
  172190. 2/28/96
  172191. DYE, J. L. THE ROLE OF CROWN AND CRYPTAND COMPLEXATION OF CATIONS IN THE FORMATION OF METAL AMINE AND METAL ETHER SOLUTIONS, P 63. PROGRESS IN MACROCYCLIC CHEMISTRY (VOL. 1, R. M. IZATT AND J. J. CHRISTENSEN, ED.) WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.
  172192. GABRIEL WEATHERHEAD
  172193. 11072
  172194. 12081N
  172195. 2/28/96
  172196. MORF, W. E.; AMMANN, D.; BISSIG, R.; PRETSCH, E.; SIMON, W. CATION SELECTIVITY OF NEUTRAL MACROCYCLIC AND NONMACROCYCLIC COMPLEXING AGENTS IN MEMBRANES, P 1. PROGRESS IN MACROCYCLIC CHEMISTRY (VOL. 1, R. M. IZATT AND J. J. CHRISTENSEN, ED.) WILEY INTERSCIENCE: NEW YORK, 1979 A REVIEW.
  172197. GABRIEL WEATHERHEAD
  172198. 11073
  172199. 12082
  172200. 2/28/96V
  172201. KEMP, D. S. RACEMIZATION IN PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172202. GABRIEL WEATHERHEAD
  172203. 11074
  172204. 12083N
  172205. 2/28/96V
  172206. MEIENHOFER, J. THE MIXED CARBONIC ANHYDRIDE METHOD OF PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172207. GABRIEL WEATHERHEAD
  172208. 11075
  172209. 12084N
  172210. 2/28/96V
  172211. RICH, D. H., SIGH, J. THE CARBODIIMIDE METHOD. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172212. GABRIEL WEATHERHEAD
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  172216. MEIENHOFER, J. THE AZIDE METHOD IN PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172217. GABRIEL WEATHERHEAD
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  172220. 2/28/96V
  172221. BODANSZKY, M. ACTIVE ESTERS IN PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172222. GABRIEL WEATHERHEAD
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  172224. 12087N
  172225. 2/28/96V
  172226. JONES, J. H. THE FORMATION OF PEPTIDE BONDS: A GENERAL SURVEY. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.a
  172227. GABRIEL WEATHERHEAD
  172228. 11079
  172229. 12088N
  172230. 2/28/96V
  172231. GROSS, E.; MEIENHOFER, J. THE PEPTIDE BOND. THE PEPTIDES (VOL. 1, MAJOR METHODS OF PEPTIDE BOND FORMATION, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1979 A REVIEW.
  172232. GABRIEL WEATHERHEAD
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  172234. 12089N
  172235. 2/28/96V
  172236. PADWA, A. PHOTOCHEMICAL TRANSFORMATIONS OF CYCLOPROPENE DERIVATIVES. ORGANIC PHOTOCHEMISTRY (VOL. 4, A. PADWA, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  172237. GABRIEL WEATHERHEAD
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  172240. 2/28/96V
  172241. HIXSON, S. S. PHOTOCHEMISTRY OF CYCLOPROPANES. ORGANIC PHOTOCHEMISTRY (VOL. 4, A. PADWA, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  172242. GABRIEL WEATHERHEAD
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  172244. 12091N
  172245. 2/28/96V
  172246. MORRISON, H. PHOTOCHEMISTRY OF NONCONJUGATED ARYL OLEFINS. ORGANIC PHOTOCHEMISTRY (VOL. 4, A. PADWA, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  172247. GABRIEL WEATHERHEAD
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  172249. 12092N
  172250. 2/28/96V
  172251. KROPP, P. J. PHOTOCHEMISTRY OF ALKENES IN SOLUTION. ORGANIC PHOTOCHEMISTRY (VOL. 4, A. PADWA, ED.), MARCEL DEKKER: NEW YORK, 1979 A REVIEW.a
  172252. GABRIEL WEATHERHEAD
  172253. 11084
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  172255. 2/28/96
  172256. MARYANOFF, B. E., HUTCHINS, R. O., MARYANOFF, C. A. STEREOCHEMICAL ASPECTS OF PHOSPHORUS CONTAINING CYCLOHEXANES. 1979,11, 187. TOPICS IN STERCOCHEMISTRY A REVIEW.a
  172257. GABRIEL WEATHERHEAD
  172258. 11085
  172259. 12094N
  172260. 2/28/96V
  172261. MALLOY, JR., T. B., BAUMAN, L. E.; CARREIRA, L. A. CONFORMATIONAL BARRIERS AND INTERCONVERSION PATHWAYS IN SOME SMALL RING MOLECULES. 1979,11, 97. TOPICS IN STERCOCHEMISTRY A REVIEW.a
  172262. GABRIEL WEATHERHEAD
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  172265. 2/28/96V
  172266. BOONE, J. R.; ASHBY, E. C. REDUCTION OF CYCLIC AND BICYCLIC KETONES BY COMPLEX METAL HYDRIDES. 1979,11, 53. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  172267. GABRIEL WEATHERHEAD
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  172269. 12096N
  172270. 2/28/96V
  172271. AARON, H. S. CONFORMATIONAL ANALYSIS OF INTRAMOLECULAR HYDROGEN BONDED COMPOUNDS IN DILUTE SOLUTION BY INFRARED SPECTROSCOPY. 1979, 11, 1. TOPICS IN STERCOCHEMISTRY A REVIEW.a
  172272. GABRIEL WEATHERHEAD
  172273. 11088
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  172275. 2/28/96VIEATON, P. E. TOWARDS DODECAHEDRANE. 1979, 35, 2189. TETRAHEDRON A REVIEW.
  172276. GABRIEL WEATHERHEAD
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  172279. 2/28/96VjABDULLA, R. F.; BRINKMEYER, R. S. THE CHEMISTRY OF FORMAMIDE ACETALS. 1979, 35,1675. TETRAHEDRON A REVIEW.a
  172280. GABRIEL WEATHERHEAD
  172281. 11090
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  172283. 2/28/96VxTASHIRO, M. SELECTIVE SYNTHESIS OF AROMATIC COMPOUNDS USING POSITIONAL PROTECTIVE GROUPS. 1979, 921. SYNTHESIS A REVIEW.a
  172284. GABRIEL WEATHERHEAD
  172285. 11091
  172286. 12100N
  172287. 2/28/96VnHABICH D., EFFENBERGER, F. PREPARATION OF ARYL  AND HETEROARYLTRIMETHYLSILANES. 1979, 841. SYNTHESIS A REVIEW.a
  172288. GABRIEL WEATHERHEAD
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  172291. 2/28/96V
  172292. CHAN, T. H.; FLEMING, I. ELECTROPHILIC SUBSTITUTION OF ORGANOSILICON COMPOUNDS
  172293. APPLICATIONS TO ORGANIC SYNTHESIS. 1979, 761. SYNTHESIS A REVIEW.a
  172294. GABRIEL WEATHERHEAD
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  172297. 2/28/96VwSHIPCHANDLER, M. T. THE UTILITY OF NITROACETIC ACID AND ITS ESTERS IN ORGANIC SYNTHESIS. 1979, 666. SYNTHESIS A REVIEW.a
  172298. GABRIEL WEATHERHEAD
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  172301. 2/28/96
  172302. MARTIN, S. F. SYNTHESIS OF ALDEHYDES, KETONES, AND CARBOXYLIC ACIDS FROM LOWER CARBONYL COMPOUNDS BY C C COUPLING REACTIONS. 1979, 633. SYNTHESIS A REVIEW.a
  172303. GABRIEL WEATHERHEAD
  172304. 11095
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  172306. 2/28/96ViMATHIAS, L. J. ESTERIFICATION AND ALKYLATION REACTIONS EMPLOYING ISOUREAS. 1979, 561. SYNTHESIS A REVIEW.a
  172307. GABRIEL WEATHERHEAD
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  172310. 2/28/96VmMCKILLOP, A., YOUNG, D. W. ORGANIC SYNTHESIS USING SUPPORTED REAGENTS
  172311. PART II. 1979, 481. SYNTHESIS A REVIEW.a
  172312. GABRIEL WEATHERHEAD
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  172315. 2/28/96V
  172316. YAMBUSHEV, F. D.; SAVIN, V. I. THE STEREOCHEMISTRY OF ORGANOARSENIC COMPOUNDS. 1979, 48, 582. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172317. GABRIEL WEATHERHEAD
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  172320. 2/28/96VSKUZNETSOV, M. A. DIAZENIUM SALTS. 1979, 48, 563. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172321. GABRIEL WEATHERHEAD
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  172323. 12108N
  172324. 2/28/96
  172325. MARDYKIN, V. P., GAPONIK, P. N., POPOV, A. F. THE ETHERATES OF ORGANOALUMINIUM COMPOUNDS. 1979, 48, 487. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172326. GABRIEL WEATHERHEAD
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  172329. 2/28/96V
  172330. MIRONOV, V. F.; SHELUDYAKOV, V. D.; KOZYUKOV, V. P. PHOSGENE IN THE CHEMISTRY OF ORGANOSILICON COMPOUNDS. 1979, 48, 473. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172331. GABRIEL WEATHERHEAD
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  172334. 2/28/96V
  172335. KHMEL'NITSKII, R. A.; TERENT'EV, P. B. DISSOCIATIVE IONIZATION OF NITRO DERIVATIVES OF ARENES AND HETEROCYCLIC COMPOUNDS. 1979, 48, 463. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172336. GABRIEL WEATHERHEAD
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  172339. 2/28/96V
  172340. BELETSKAYA, I. P.; DROZD, V. N. A NEW MECHANISM OF NUCLEOPHILIC SUBSTITUTION. 1979, 48, 431. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172341. GABRIEL WEATHERHEAD
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  172344. 2/28/96V
  172345. SADEKOV, I. S., BUSHKOV, A. YA.; MINKIN, V. I. THE SYNTHESIS AND STRUCTURE OF TELLURANES. 1979, 48, 343. RUSSIAN CHEMICAL REVIEWS A REVIEW.
  172346. GABRIEL WEATHERHEAD
  172347. 11104
  172348. 12113N
  172349. 2/28/96V
  172350. KALINKIN, M. I.; KOLOMNIKOVA, G. D.; PARNES, Z. N.; KURSANOV, D. N. CATALYTIC IONIC HYDROGENATION. 1979, 48, 332. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172351. GABRIEL WEATHERHEAD
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  172354. 2/28/96VhSOKOLOV, S. D. ADVANCES IN THE CHEMISTRY OF 1,2 AZOLES. 1979, 48 289. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172355. GABRIEL WEATHERHEAD
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  172358. 2/28/96V
  172359. MOVSUM ZADE, E. M. PREPARATION AND REACTIONS OF CHLORO DERIVATIVES OF NITRILES. 1979, 48, 282. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172360. GABRIEL WEATHERHEAD
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  172363. 2/28/96V
  172364. SKVORTSOV, I. M. ADVANCES IN THE STUDY OF THE STEREOCHEMISTRY OF QUINOLIZIDINES, INDOLIZIDINES, AND PYRROLIZIDINES. 1979, 48, 262. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172365. GABRIEL WEATHERHEAD
  172366. 11108
  172367. 12117N
  172368. 2/28/96
  172369. NESMEYANOV, A. N.; RYBINSKAYA, M. I.; RYBIN, L. V. DINUCLEAR IRON CARBONYL COMPLEXES WITH NITROGEN CONTAINING BRIDGES. 1979, 48, 213. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172370. GABRIEL WEATHERHEAD
  172371. 11109
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  172373. 2/28/96VoMOGILEVICH, M. M. OXIDATIVE POLYMERIZATION OF VINYL MONOMERS. 1979, 48, 199. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172374. GABRIEL WEATHERHEAD
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  172377. 2/28/96V
  172378. TEPLYAKOV, M. M. TRIMERISATION POLYCONDENSATION OF AROMATIC ACETYL COMPOUNDS AND THEIR KETALS. 1979, 48, 189. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172379. GABRIEL WEATHERHEAD
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  172381. 12120N
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  172383. SHAINYAN, B. A.; MIRSKOVA, A. N. THE CARBON NITROGEN TRIAD PROTOTROPIC TAUTOMERISM. 1979, 48,107. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  172384. GABRIEL WEATHERHEAD
  172385. 11112
  172386. 12121N
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  172388. SCHMIDT, U.; HAUSLER, J.; OHLER, E.; POISEL, H. DEHYDROAMINO ACIDS, ALPHA HYDROXY ALPHA AMINO ACIDS AND ALPHA MERCAPTO ALPHA AMINO ACIDS. 1979, 37, 251. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  172389. GABRIEL WEATHERHEAD
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  172393. MCNEIL, M.; DARVILL, A. G.; ALBERSHEIM, P. THE STRUCTURAL POLYMERS OF THE PRIMARY CELL WALLS OF DICOTS. 1979, 37,191. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  172394. GABRIEL WEATHERHEAD
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  172398. BRAND, J. M.; YOUNG, J. CHR.; SILVERSTEIN R. M. INSECT PHEROMONES: A CRITICAL REVIEW OF RECENT ADVANCES IN THEIR CHEMISTRY, BIOLOGY, AND APPLICATION. 1979, 37,1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  172399. GABRIEL WEATHERHEAD
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  172401. 12124N
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  172403. WRAY, V. CARBON CARBON COUPLING CONSTANTS: A COMPILATION OF DATA AND A PRACTICAL GUIDE. 1979, 13, 177. PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  172404. GABRIEL WEATHERHEAD
  172405. 11116
  172406. 12125N
  172407. 2/28/96VrYOUNG, R. N. NMR SPECTROSCOPY OF CARBANIONS AND CARBOCATIONS. 1978,12, 261. PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  172408. GABRIEL WEATHERHEAD
  172409. 11117
  172410. 12126N
  172411. 2/28/96VrWRACKMEYER, B. CARBON 13 NMR SPECTROSCOPY OF BORON COMPOUNDS. 1978,12, 227. PROGRESS IN NMR SPECTROSCOPY A REVIEW.a
  172412. GABRIEL WEATHERHEAD
  172413. 11118
  172414. 12127N
  172415. 2/28/96VqBURKE, S. D.; GRIECO, P. A. INTRAMOLECULAR REACTIONS OF DIAZOCARBONYL. 1979, 26, 361. ORGANIC REACTIONS A REVIEW.a
  172416. GABRIEL WEATHERHEAD
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  172419. 2/28/96VnGSCHWEND, H. W., RODRIGUEZ, H. R. HETEROATOM FACILITATED LITHIATIONS. 1979, 26, 1. ORGANIC REACTIONS A REVIEW.a
  172420. GABRIEL WEATHERHEAD
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  172423. 2/28/96VpJUARISTI, E. THE ATTRACTIVE AND REPULSIVE GAUCHE EFFECTS. 1979, 56, 438. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  172424. GABRIEL WEATHERHEAD
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  172427. 2/28/96
  172428. VlKINGSBURY C. A. CONFORMATIONS OF SUBSTITUTED ETHANES. 1979, 56, 431. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  172429. GABRIEL WEATHERHEAD
  172430. 11122
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  172432. 2/28/96V`KASHIMA, C. SYNTHETIC REACTIONS USING ISOXAZOLE COMPOUNDS. 1979,12, 1343. HETEROCYCLES A REVIEW.a
  172433. GABRIEL WEATHERHEAD
  172434. 11123
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  172436. 2/28/96VWSLIWA, W. 1,10 PHENANTBROLINE AND ITS COMPLEXES. 1979, 12, 1207. HETEROCYCLES A REVIEW.a
  172437. GABRIEL WEATHERHEAD
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  172440. 2/28/96V
  172441. TSUGE, O. SYNTHESIS OF HETEROCYCLES USING HETEROCUMULENES CONJUGATED WITH THE CARBONYL GROUP. 1979, 12, 1067. HETEROCYCLES A REVIEW.a
  172442. GABRIEL WEATHERHEAD
  172443. 11125
  172444. 12134N
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  172446. RAKHMANKULOV, D. L.; KANTOR, E. A.; KARAKHANOV, R. A. ACID CATALYZED TRANSFORMATIONS IN 1,3 DIOXACYCLANES IN LIQUID PHASE. 1979, 12, 1039. HETEROCYCLES A REVIEW.a
  172447. GABRIEL WEATHERHEAD
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  172449. 12135N
  172450. 2/28/96
  172451. WEINREB, S. M.; LEVIN, J. I. SYNTHESIS OF NITROGEN CONTAINING HETEROCYCLES BY THE IMINO DIELS ALDER REACTION. 1979, 12, 949. HETEROCYCLES A REVIEW.a
  172452. GABRIEL WEATHERHEAD
  172453. 11127
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  172455. 2/28/96VsKHAN, M. A., DA ROCHA, J. F. PYRROLOQUINOLINES V. 1H PYRROLO[3,2 C]QUINOLINES. 1979,12, 857. HETEROCYCLES A REVIEW.a
  172456. GABRIEL WEATHERHEAD
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  172460. HAYASHI, E.; HIGASHINO, T. REACTIONS OF AROMATIC HETEROCYCLES INVOLVING THE CATALYTIC ACTIONS OF THE CYANIDE ION. 1979,12, 837. HETEROCYCLES A REVIEW.a
  172461. GABRIEL WEATHERHEAD
  172462. 11129
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  172464. 2/28/96VlABOU GHARBIA, M. A. JOULLIE, M. M. REACTIONS OF NITRONES WITH KETENES. 1979, 12, 819. HETEROCYCLES A REVIEW.a
  172465. GABRIEL WEATHERHEAD
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  172468. 2/28/96VSSLIWA, W.; ZAMARLIK, H. POLYAZAPHENANTHRENES. 1979, 12, 529. HETEROCYCLES A REVIEW.a
  172469. GABRIEL WEATHERHEAD
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  172472. 2/28/96
  172473. VuAFZAL, M.; AL HASSAN, J. M. PROTON MAGNETIC RESONANCE SPECTRA OF PHYTOXANTHONES. 1979,12, 421. HETEROCYCLES A REVIEW.a
  172474. GABRIEL WEATHERHEAD
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  172477. 2/28/96VwAFZAL, M.; AL HASSAN, J. M.; AL MASAD, F. N. ABSORPTION SPECTRA OF PHYTOXANTHONES. 1979,12, 269. HETEROCYCLES A REVIEW.a
  172478. GABRIEL WEATHERHEAD
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  172482. MEZHERITSKII, V. V.; WASSERMAN, A. L.; DOROFEENKO, G. N. REACTIONS OF ALPHA  AND GAMMA AIKYL GROUPS IN PYRYLIUM SALTS AND SOME TRANSFORMATIONS AND REACTION PRODUCTS. 1979, 12, 51. HETEROCYCLES A REVIEW.a
  172483. GABRIEL WEATHERHEAD
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  172486. 2/28/96VbELLIOTT M. PROGRESS IN THE DESIGN OF NEW INSECTICIDES. 1979, 757. CHEMISTRY AND INDUSTRY A REVIEW.a
  172487. GABRIEL WEATHERHEAD
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  172490. 2/28/96VZHODGE, P. POLYMER SUPPORTED PROTECTING GROUPS. 1979, 624. CHEMISTRY AND INDUSTRY A REVIEW.a
  172491. GABRIEL WEATHERHEAD
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  172493. 12145N
  172494. 2/28/96
  172495. V`HARDY, P. M. PROTECTING GROUPS IN PEPTIDE SYNTHESIS. 1979, 617. CHEMISTRY AND INDUSTRY A REVIEW.a
  172496. GABRIEL WEATHERHEAD
  172497. 11137
  172498. 12146N
  172499. 2/28/96VgHASLAM, E. ACTIVATION AND PROTECTION OF THE CARBONYL GROUP. 1979, 610. CHEMISTRY AND INDUSTRY A REVIEW.a
  172500. GABRIEL WEATHERHEAD
  172501. 11138
  172502. 12147N
  172503. 2/28/96VhMCOMIE, J. F. W. RECENT DEVELOPMENTS WITH PROTECTING GROUPS. 1979, 603. CHEMISTRY AND INDUSTRY A REVIEW.a
  172504. GABRIEL WEATHERHEAD
  172505. 11139
  172506. 12148N
  172507. 2/28/96V|DOWLE, M. D.; DAVIES, D. I. SYNTHESIS AND SYNTHETIC UTILITY OF HALOLACTONES. 1979, 8,171. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  172508. GABRIEL WEATHERHEAD
  172509. 11140
  172510. 12149N
  172511. 2/28/96V
  172512. NORMAN, R. 0. C. APPLICATIONS OF E.S.R. SPECTROSCOPY TO KINETICS AND MECHANISM IN ORGANIC CHEMISTRY. 1979, 8,1. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  172513. GABRIEL WEATHERHEAD
  172514. 11141
  172515. 12150N
  172516. 2/28/96V@HART, H. SIMPLE ENOLS. 1979, 79, 515. CHEMICAL REVIEWS A REVIEW.a
  172517. GABRIEL WEATHERHEAD
  172518. 11142
  172519. 12151N
  172520. 2/28/96ViCLODE D. M. CARBOHYDRATE CYCLIC ACETAL FORMATION AND MIGRATION. 1979, 79, 491. CHEMICAL REVIEWS A REVIEW.a
  172521. GABRIEL WEATHERHEAD
  172522. 11143
  172523. 12152N
  172524. 2/28/96V
  172525. MUETTERTIES, E. L.; STEIN, J. MECHANISTIC FEATURES OF CATALYTIC CARBON MONOXIDE HYDROGENATION REACTIONS. 1979, 79, 479. CHEMICAL REVIEWS A REVIEW.a
  172526. GABRIEL WEATHERHEAD
  172527. 11144
  172528. 12153N
  172529. 2/28/96VlGEORGE, M. V.; BHAT V. PHOTOOXYGENATIONS OF NITROGEN HETEROCYCLES. 1979, 79, 447. CHEMICAL REVIEWS A REVIEW.a
  172530. GABRIEL WEATHERHEAD
  172531. 11145
  172532. 12154N
  172533. 2/28/96V
  172534. FRIMER, A. A. THE REACTIONS OF SINGLET OXYGEN WITH OLEFINS: THE QUESTION OF MECHANISM. 1979, 79, 359. CHEMICAL REVIEWS A REVIEW.a
  172535. GABRIEL WEATHERHEAD
  172536. 11146
  172537. 12155N
  172538. 2/28/96VsCROMWELL, N.; PHILLIPS, B. THE AZETIDINES. RECENT SYNTHETIC DEVELOPMENTS. 1979, 79, 331. CHEMICAL REVIEWS A REVIEW.a
  172539. GABRIEL WEATHERHEAD
  172540. 11147
  172541. 12156N
  172542. 2/28/96
  172543. V{TRAYNHAM, J. G. IPSO SUBSTITUTION IN FREE RADICAL AROMATIC SUBSTITUTION REACTIONS. 1979, 79 323. CHEMICAL REVIEWS A REVIEW.a
  172544. GABRIEL WEATHERHEAD
  172545. 11148
  172546. 12157N
  172547. 2/28/96V
  172548. OMAE, I. ORGANOMETALLIC INTRAMOLECULAR COORDINATION COMPOUNDS CONTAINING A NITROGEN DONOR LIGAND. 1979, 79, 287. CHEMICAL REVIEWS A REVIEW.a
  172549. GABRIEL WEATHERHEAD
  172550. 11149
  172551. 12158N
  172552. 2/28/96V
  172553. VIEHE, H. G.; MERENYI, R.; STELLA, L.; JANOUSEK, Z. CAPTO DATIVE SUBSTITUENT EFFECTS IN SYNTHESES WITH RADICALS AND RADICOPHILES [NEW SYNTHETIC METHODS (32)]. 1979, 18, 917. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172554. GABRIEL WEATHERHEAD
  172555. 11150
  172556. 12159N
  172557. 2/28/96V
  172558. IDDON, B., METH COHN, O., SCRIVEN, E. F. V., SUSCHITZKY H.; GALLAGHER, P. T. DEVELOPMENTS IN ARYLNITRENE CHEMISTRY: SYNTHESES AND MECHAMISMS [NEW SYNTHETIC METHODS (31)]. 1979, 18, 900. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172559. GABRIEL WEATHERHEAD
  172560. 11151
  172561. 12160N
  172562. 2/28/96
  172563. LOZAC'H, N.; GOODSON, A. L.; POWELL, W. H. NODAL NOMENCLATURE
  172564. GENERAL PRINCIPLES. 1979, 18, 887. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172565. GABRIEL WEATHERHEAD
  172566. 11152
  172567. 12161N
  172568. 2/28/96V
  172569. ACHER, R. NEUROPHYSINS: MOLECULAR AND CELLULAR ASPECTS. 1979, 18, 846. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172570. GABRIEL WEATHERHEAD
  172571. 11153
  172572. 12162N
  172573. 2/28/96V
  172574. MURAI, S., SONODA, N. CATALYTIC REACTIONS WITH HYDROSILAME AND CARBON MONOXIDE [NEW SYNTHETIC METHODS (30)]. 1979, 18, 837. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172575. GABRIEL WEATHERHEAD
  172576. 11154
  172577. 12163N
  172578. 2/28/96V
  172579. KLESSINGER, M.; RADEMACHER, P. CONFORMATIONAL ANALYSIS BY PHOTOELECTRON SPECTROSCOPY. 1979,18, 826. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172580. GABRIEL WEATHERHEAD
  172581. 11155
  172582. 12164N
  172583. 2/28/96
  172584. DE MEIJERE, A. BONDING PROPERTIES OF CYCLOPROPANE AND THEIR CHEMICAL CONSEQUENCES. 1979,18, 809. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172585. GABRIEL WEATHERHEAD
  172586. 11156
  172587. 12165N
  172588. 2/28/96V
  172589. VOGTLE, F.; WEBER, E. MULTIDENTATE ACYCLIC NEUTRAL LIGANDS AND THEIR COMPLEXATION. 1979, 18, 753. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172590. GABRIEL WEATHERHEAD
  172591. 11157
  172592. 12166N
  172593. 2/28/96V
  172594. BIANCHI, G.; DE MICHELI, C.; GANDOLFI, R. 1,3 DIPOLAR CYCLOREVERSIONS. 1979, 18, 721. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172595. GABRIEL WEATHERHEAD
  172596. 11158
  172597. 12167N
  172598. 2/28/96V
  172599. MUKAIYAMA, T. NEW SYNTHETIC REACTIONS BASED ON THE ONIUM SALTS OF AZA ARENES [NEW SYNTHETIC METHODS (29)]. 1979, 18, 707. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172600. GABRIEL WEATHERHEAD
  172601. 11159
  172602. 12168N
  172603. 2/28/96
  172604. VyDYE, J. L. COMPOUNDS OF ALKALI METAL ANIONS. 1979, 18, 587. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172605. GABRIEL WEATHERHEAD
  172606. 11160
  172607. 12169N
  172608. 2/28/96V
  172609. TURRO, N. J.; MCVEY, J.; RAMAMURTHY, V.; LECHTKEN, P. ADIABATIC PHOTOREACTIONS OF ORGANIC MOLECULES. 1979, 18, 572. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172610. GABRIEL WEATHERHEAD
  172611. 11161
  172612. 12170N
  172613. 2/28/96V
  172614. HOFFMANN, R. W. STEREOCHEMISTRY OF [2.3]SIGMATROPIC REARRANGEMENTS. 1979, 18, 563. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172615. GABRIEL WEATHERHEAD
  172616. 11162
  172617. 12171N
  172618. 2/28/96V
  172619. VOGTLE, F.; ROSSA, L. PYROLYSIS OF SULFONES AS A SYNTHETIC METHOD [NEW SYNTHETIC METHODS (28)]. 1979, 18, 514. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172620. GABRIEL WEATHERHEAD
  172621. 11163
  172622. 12172N
  172623. 2/28/96
  172624. BARKER, B. J., ROSENFARB, J., CARUSO, J. A. UREAS AS SOLVENTS FOR CHEMICAL INVESTIGATIONS. 1979, 18, 503. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172625. GABRIEL WEATHERHEAD
  172626. 11164
  172627. 12173N
  172628. 2/28/96V
  172629. MANGOLD H. K. SYNTHESIS AND BIOSYNTHESIS OF ALKOXYLIPIDS. I979, 18, 493. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  172630. GABRIEL WEATHERHEAD
  172631. 11165
  172632. 12174N
  172633. 2/28/96V
  172634. SHARPLESS, K. B., VERHOEVEN T. R. SELECTIVE OXYGENATION WITH TERT BUTYL HYDROPEROXIDE. 1979,12, 63. ALDRICHIMICA ACTA A REVIEW.a
  172635. GABRIEL WEATHERHEAD
  172636. 11166
  172637. 12175N
  172638. 2/28/96V[OLAH, G. A. NEW SYNTHETIC REAGENTS AND REACTIONS. 1979, 12, 43. ALDRICHIMICA ACTA A REVIEW.a
  172639. GABRIEL WEATHERHEAD
  172640. 11167
  172641. 12176N
  172642. 2/28/96V
  172643. KATRITZKY, A. R.; JONES, P. M. THE LITERATURE OF HETEROCYCLIC  CHEMISTRY, PART 2. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172644. GABRIEL WEATHERHEAD
  172645. 11168
  172646. 12177N
  172647. 2/28/96
  172648. HANSON, P. HETEROAROMATIC RADICALS, PART ONE: GENERAL PROPERTIES; RADICALS WITH GROUP V RING HETEROATOMS. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172649. GABRIEL WEATHERHEAD
  172650. 11169
  172651. 12178N
  172652. 2/28/96VvWAKEFIELD, B. J., WRIGHT, D. J. ISOXAZOLE CHEMISTRY SINCE 1963. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172653. GABRIEL WEATHERHEAD
  172654. 11170
  172655. 12179N
  172656. 2/28/96V
  172657. RAJAPPA, S.; NAIR, M. D. RING SYNTHESIS OF HETEROAROMATIC NITRO COMPOUNDS. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172658. GABRIEL WEATHERHEAD
  172659. 11171
  172660. 12180N
  172661. 2/28/96VaNEWKOME, G. R.; NAYAK, A. THIAZOLIDINONES. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172662. GABRIEL WEATHERHEAD
  172663. 11172
  172664. 12181N
  172665. 2/28/96V_BUNTING, J. W. HETEROCYCLIC PSEUDOBASES. 1979, 25. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172666. GABRIEL WEATHERHEAD
  172667. 11173
  172668. 12182N
  172669. 2/28/96
  172670. V~TISLER, M.; STANOVNIK, B. RECENT ADVANCES IN PYRIDAZINE CHEMISTRY. 1979, 24, 363. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172671. GABRIEL WEATHERHEAD
  172672. 11174
  172673. 12183N
  172674. 2/28/96VxSTOODLEY, R. J. 1,4 THIAZINES AND THEIR DIHYDRO DERIVATIVES. 1979, 24, 294. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172675. GABRIEL WEATHERHEAD
  172676. 11175
  172677. 12184N
  172678. 2/28/96VnROBINS, D. J. ADVANCES IN PYRROLIZIDINE CHEMISTRY. 1979, 24, 248. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172679. GABRIEL WEATHERHEAD
  172680. 11176
  172681. 12185N
  172682. 2/28/96V
  172683. LISTER, J. H. CURRENT VIEWS ON SOME PHYSICOCHEMICAL ASPECTS OF PURINES. 1979, 24, 215. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172684. GABRIEL WEATHERHEAD
  172685. 11177
  172686. 12186N
  172687. 2/28/96V
  172688. POPP, F. D. DEVELOPMENTS IN THE CHEMISTRY OF REISSERT COMPOUNDS (1968 1978). 1979, 24, 187. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172689. GABRIEL WEATHERHEAD
  172690. 11178
  172691. 12187N
  172692. 2/28/96
  172693. V]BARTON, J. W. BENZO[C]CINNOLINES. 1979, 24, 152. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172694. GABRIEL WEATHERHEAD
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  172696. 12188N
  172697. 2/28/96V
  172698. LALEZARI, I., SHAFIEE, A., YALPANI, M. SELENIUM NITROGEN HETEROCYCLES. 1979, 24, 109. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172699. GABRIEL WEATHERHEAD
  172700. 11180
  172701. 12189N
  172702. 2/28/96VqSCHMITZ, E. THREE MEMBERED RINGS WITH TWO HETEROATOMS. 1979, 24, 63. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172703. GABRIEL WEATHERHEAD
  172704. 11181
  172705. 12190N
  172706. 2/28/96VYARMAREGO, W. L. F. QUINAZOLINES. 1979, 24,1. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  172707. GABRIEL WEATHERHEAD
  172708. 11182
  172709. 12191N
  172710. 2/28/96V
  172711. ASMUS, K. D. STABILIZATION OF OXIDIZED SULFUR CENTERS IN ORGANIC SULFIDES. RADICAL CATIONS AND ODD ELECTRON SULFUR SULFUR BONDS. 1979,12, 436. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172712. GABRIEL WEATHERHEAD
  172713. 11183
  172714. 12192N
  172715. 2/28/96
  172716. BACIOCCHI, E. BASE DEPENDENCE OF TRANSITION STATE STRUCTURE IN ALKENE FORMING E2 REACTIONS. 1979,12, 430. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172717. GABRIEL WEATHERHEAD
  172718. 11184
  172719. 12193N
  172720. 2/28/96V
  172721. LEONARD, N. J. TRIMETHYLENE BRIDGES AS SYNTHETIC SPACERS FOR THE DETECTION OF INTRAMOLECULAR INTERACTIONS. 1979,12, 423. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172722. GABRIEL WEATHERHEAD
  172723. 11185
  172724. 12194N
  172725. 2/28/96V`TUFARIELLO, J. J. ALKALOIDS FROM NITRONES. 1979,12, 396. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172726. GABRIEL WEATHERHEAD
  172727. 11186
  172728. 12195N
  172729. 2/28/96VoADAM, W. OXYGEN DIRADICALS DERIVED FROM CYCLIC PEROXIDES. 1979,12, 390. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172730. GABRIEL WEATHERHEAD
  172731. 11187
  172732. 12196N
  172733. 2/28/96VvMORRISON, H. PHOTOCHEMISTRY OF ORGANIC BICHROMOPHORIC MOLECULES. 1979,12, 383. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172734. GABRIEL WEATHERHEAD
  172735. 11188
  172736. 12197N
  172737. 2/28/96
  172738. )VlSMITH, K. M. PROTOPORPHYRIN IX: SOME RECENT RESEARCH. 1979, 12, 374. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172739. GABRIEL WEATHERHEAD
  172740. 11189
  172741. 12198N
  172742. 2/28/96VnSCHUSTER, G. B. CHEMILUMINESCENCE OF ORGANIC PEROXIDES. 1979, 12, 366. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172743. GABRIEL WEATHERHEAD
  172744. 11190
  172745. 12199N
  172746. 2/28/96V
  172747. DAVES, JR., G. D. MASS SPECTROMETRY OF INVOLATILE AND THERMALLY UNSTABLE MOLECULES. 1979,12, 359. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172748. GABRIEL WEATHERHEAD
  172749. 11191
  172750. 12200N
  172751. 2/28/96V
  172752. MUETTERTIES, E. L.; BLEEKE, J. R. CATALYTIC HYDROGENATION OF AROMATIC HYDROCARBONS. 1979,12, 324. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172753. GABRIEL WEATHERHEAD
  172754. 11192
  172755. 12201N
  172756. 2/28/96V
  172757. LAMBERT, J. B.; MARK, H. W.; HOLCOMB, A. G.; MAGYAR, E. S. INDUCTIVE ENHANCEMENT OF NEIGHBORING GROUP PARTICIPATION. 1979,12, 317. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172758. GABRIEL WEATHERHEAD
  172759. 11193
  172760. 12202N
  172761. 2/28/96
  172762. .VtPADWA, A. EXCITED STATE CHEMISTRY OF CYCLOPROPENE DERIVATIVES. 1979,12, 310. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172763. GABRIEL WEATHERHEAD
  172764. 11194
  172765. 12203N
  172766. 2/28/96V
  172767. SCHAEFER III, H. F. THE 1,2 HYDROGEN SHIFT: A COMMON VEHICLE FOR THE DISAPPEARANCE OF EVANESCENT MOLECULAR SPECIES. 1979,12, 288. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172768. GABRIEL WEATHERHEAD
  172769. 11195
  172770. 12204N
  172771. 2/28/96V
  172772. SMIT, W. A.; ZEFIROV, N. S.; BODRIKOV, 1. V.; KRIMER, M. Z. EPISULFONIUM IONS: MYTH AND REALITY. 1979,12, 282. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172773. GABRIEL WEATHERHEAD
  172774. 11196
  172775. 12205N
  172776. 2/28/96V
  172777. MADIX, R. J. SURFACE REACTIVITY: HETEROGENEOUS REACTIONS ON SINGLE CRYSTAL SURFACES. 1979,12, 265. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172778. GABRIEL WEATHERHEAD
  172779. 11197
  172780. 12206N
  172781. 2/28/96V
  172782. BRUNNER, H. OPTICAL INDUCTION IN ORGANO TRANSITION METAL COMPOUNDS AND ASYMMETRIC CATALYSIS. 1979,12, 250. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172783. GABRIEL WEATHERHEAD
  172784. 11198
  172785. 12207N
  172786. 2/28/96VxBENSON, S. W.; NANGIA, P. S. PROBLEMS IN OXIDATION AND COMBUSTION. 1979,12, 223. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  172787. GABRIEL WEATHERHEAD
  172788. 11199
  172789. 12208N
  172790. 2/28/96V`TSUJI, J. ORGANIC SYNTHESIS WITH PALLADIUM COMPOUNDS. SPRINGER VERLAG: NEW YORK, 1980. A REVIEW.a
  172791. GABRIEL WEATHERHEAD
  172792. 11200
  172793. 12209N
  172794. 2/28/96V~TSANG, W.; GRIFFIN, G. W. METABOLIC ACTIVATION OF POLYNUCLEAR AROMATIC HYDROCARBONS. PERGAMON PRESS: NEW YORK, 1979. A REVIEW.a
  172795. GABRIEL WEATHERHEAD
  172796. 11201
  172797. 12210N
  172798. 2/28/96V
  172799. SERJEANT, E. P.; DEMPSEY, B. IONIZATION CONSTANTS OF ORGANIC ACIDS IN AQUEOUS SOLUTION. PERGAMON PRESS: NEW YORK, 1979. A REVIEW.a
  172800. GABRIEL WEATHERHEAD
  172801. 11202
  172802. 12211N
  172803. 2/28/96V
  172804. SCHEITHAUER, ST., MAYER, R. THIO  AND DITHIOCARBOLCYLIC ACIDS AND THEIR DERIVATIVES. HEYDEN & SON: PHILADELPHIA, 1979. A REVIEW.a
  172805. GABRIEL WEATHERHEAD
  172806. 11203
  172807. 12212N
  172808. 2/28/96
  172809. 8VbREUTOV, O. A.; BELETSKAYA, I. P.; BUTIN, K. P. CH ACIDS. PERGAMON PRESS: NEW YORK, 1979. A REVIEW.a
  172810. GABRIEL WEATHERHEAD
  172811. 11204
  172812. 12213N
  172813. 2/28/96V}PERRIN, D. D., ARMAREGO, W. L., PERRIN, D. R. PURIFICATION OF LABORATORY CHEMICALS. PERGAMON PRESS: NEW YORK, 1980. A REVIEW.a
  172814. GABRIEL WEATHERHEAD
  172815. 11205
  172816. 12214N
  172817. 2/28/96V
  172818. PATAI, S., ED. THE CHEMISTRY OF KETENES, ALLENES, AND RELATED COMPOUNDS. PARTS 1 AND 2. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  172819. GABRIEL WEATHERHEAD
  172820. 11206
  172821. 12215N
  172822. 2/28/96V
  172823. PARSHALL, G. W. HOMOGENEOUS CATALYSIS. THE APPLICATIONS AND CHEMISTRY OF SOLUBLE TRANSITION METAL COMPLEXES. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  172824. GABRIEL WEATHERHEAD
  172825. 11207
  172826. 12216N
  172827. 2/28/96VhNORGRADI, M. STEREOCHEMISTRY: BASIC CONCEPTS AND APPLICATIONS. PERGAMON PRESS: NEW YORK, 1980. A REVIEW.a
  172828. GABRIEL WEATHERHEAD
  172829. 11208
  172830. 12217N
  172831. 2/28/96
  172832. =V~MATHUR, N. K., NARANG, C. K.; WILLIAMS, R. E. POLYMERS AS AIDS IN ORGANIC CHEMISTRY. ACADEMIC PRESS: NEW YORK, 1980. A REVIEW.a
  172833. GABRIEL WEATHERHEAD
  172834. 11209
  172835. 12218N
  172836. 2/28/96V
  172837. KOCHETKOV, N. K.; KUDRJASHOV, L. I.; CHLENOV, M. A. RADIATION CHEMISTRY OF CARBOHYDRATES. PERGAMON PRESS: NEW YORK, 1979. A REVIEW.a
  172838. GABRIEL WEATHERHEAD
  172839. 11210
  172840. 12219N
  172841. 2/28/96V
  172842. FABIANA, J.; HARTMANN, H. LIGHT ABSORPTION OF ORGANIC COLORANTS (CONCEPTS IN ORGANIC CHEMISTRY, VOL. 12). SPRINGER VERLAG: NEW YORK, 1980. A REVIEW.a
  172843. GABRIEL WEATHERHEAD
  172844. 11211
  172845. 12220N
  172846. 2/28/96V
  172847. DEHMLOW, E., DEHMLOW, S. PHASE TRANSFER CATALYSIS (MONOGRAPHS IN MODERN CHEMISTRY, VOL. 11). VERLAG CHEMIE: WEINHEIM, 1980. A REVIEW.a
  172848. GABRIEL WEATHERHEAD
  172849. 11212
  172850. 12221N
  172851. 2/28/96V
  172852. COLLMAN, J. P., HEGEDUS, L. S. PRINCIPLES AND APPLICATIONS OF ORGANOTRANSITION METAL CHEMISTRY. UNIVERSITY SCIENCE BOOKS: CALIFORNIA, 1980 A REVIEW.a
  172853. GABRIEL WEATHERHEAD
  172854. 11213
  172855. 12222
  172856. 2/28/96V
  172857. BROWN, R. F. C. PYROLYTIC METHODS IN ORGANIC CHEMISTRY. APPLICATIONS OF FLOW AND F. V. P. TECHNIQUES. ACADEMIC PRESS: NEW YORK, 1980. A REVIEW.a
  172858. GABRIEL WEATHERHEAD
  172859. 11214
  172860. 12223N
  172861. 2/28/96VkBOCHKOV, A. F.; ZAIKOV, G. E. CHEMISTRY OF THE O GLYCOSIDIC BOND. PERGAMON PRESS: NEW YORK, 1979. A REVIEW.a
  172862. GABRIEL WEATHERHEAD
  172863. 11215
  172864. 12224N
  172865. 2/28/96V
  172866. ANH, N. T. REGIO  AND STEREO SELECTIVITIES IN SOME NUCLEOPHILIC REACTIONS. 1980, 88. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172867. GABRIEL WEATHERHEAD
  172868. 11216
  172869. 12225N
  172870. 2/28/96V
  172871. MUSZKAT, K. A. THE 4A,7B DIHYDROPHENANTHRENES. 1980, 88. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172872. GABRIEL WEATHERHEAD
  172873. 11217
  172874. 12226N
  172875. 2/28/96
  172876. BIRKHOFER, L.; STUHL, O. SILYLATED SYNTHONS
  172877. FACILE ORGANIC REAGENTS OF GREAT APPLICABILITY. 1980, 88. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172878. GABRIEL WEATHERHEAD
  172879. 11218
  172880. 12227N
  172881. 2/28/96V
  172882. RUCHARDT, C. STERIC EFFECTS IN FREE RADICAL CHEMISTRY. 1980, 88. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172883. GABRIEL WEATHERHEAD
  172884. 11219
  172885. 12228N
  172886. 2/28/96V
  172887. GLEITER, R. PHOTOELECTRON SPECTRA AND BONDING IN SMALL RING HYDROCARBONS. 1980, 86,197. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172888. GABRIEL WEATHERHEAD
  172889. 11220
  172890. 12229N
  172891. 2/28/96V
  172892. GIEITER, R.; SPANGET LARSEN, J. SOME OF ASPECTS OF THE PHOTOELECTRON SPECTROSCOPY OF ORGANIC SULFUR COMPOUNDS. 1980, 86, 139. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172893. GABRIEL WEATHERHEAD
  172894. 11221
  172895. 12230N
  172896. 2/28/96V
  172897. SANDORFY, C. FAR ULTRAVIOLET ABSORPTION SPECTRA OF ORGANIC MOLECULES: VALENCE SHELL AND RYDBERG TRANSITIONS. 1980 86, 91. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  172898. GABRIEL WEATHERHEAD
  172899. 11222
  172900. 12231N
  172901. 2/28/96
  172902. KOVACS, J. RACEMIZATION AND COUPLING RATES OF N2 PROTECTED AMINO ACID AND PEPTIDE ACTIVE ESTERS: PREDICTIVE POTENTIAL. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.
  172903. GABRIEL WEATHERHEAD
  172904. 11223
  172905. 12232N
  172906. 2/28/96V
  172907. SHEPPARD, R. C. PARTIAL SYNTHESIS OF PEPTIDES AND PROTEINS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172908. GABRIEL WEATHERHEAD
  172909. 11224
  172910. 12233N
  172911. 2/28/96
  172912. KISFALUDY, L. PROTEINS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172913. GABRIEL WEATHERHEAD
  172914. 11225
  172915. 12234N
  172916. 2/28/96V
  172917. MUKAIYAMI, T.; MATSUEDA, R.; UEKI, M. THE OXIDATION REDUCTION CONDENSATION. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172918. GABRIEL WEATHERHEAD
  172919. 11226
  172920. 12235N
  172921. 2/28/96V
  172922. UGI, I. THE FOUR COMPONENT SYNTHESIS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172923. GABRIEL WEATHERHEAD
  172924. 11227
  172925. 12236N
  172926. 2/28/96V
  172927. FRIDKIN, M. POLYMERIC REAGENTS IN PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172928. GABRIEL WEATHERHEAD
  172929. 11228
  172930. 12237N
  172931. 2/28/96V
  172932. MUTTER, M.; BAYER, E. THE LIQUID PHASE METHOD FOR PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172933. GABRIEL WEATHERHEAD
  172934. 11229
  172935. 12238N
  172936. 2/28/96V
  172937. BARANY, G.; MERRIFIELD, R. B. SOLID PHASE PEPTIDE SYNTHESIS. THE PEPTIDES (VOL. 2, SPECIAL METHODS IN PEPTIDE SYNTHESIS, PART A, E. GROSS AND J. MEIENHOFER, EDS.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172938. GABRIEL WEATHERHEAD
  172939. 11230
  172940. 12239N
  172941. 2/28/96V
  172942. SNIECKUS, V. HETEROCYCLIC COMPOUNDS IN ALKALOID SYNTHESIS. SURVEY OF PROGRESS IN CHEMISTRY (VOL. 9, A. F. SCOTT, ED.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172943. GABRIEL WEATHERHEAD
  172944. 11231
  172945. 12240N
  172946. 2/28/96V
  172947. MAKOSZA, M. TWO PHASE REACTIONS IN ORGANIC CHEMISTRY SURVEY OF PROGRESS IN CHEMISTRY (VOL. 9, A. F. SCOTT, ED.), ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172948. GABRIEL WEATHERHEAD
  172949. 11232
  172950. 12241N
  172951. 2/28/96
  172952. LITKEI, GY. CHALCONE EPOXIDES IN FLAVONOID CHEMISTRY. RECENT DEVELOPMENTS IN THE CHEMISTRY OF NATURAL CARBON COMPOUNDS (VOL. 9, R. BOGNAR, V. BRUCKNER, AND CS. SZANTAY, EDS.), HEYDEN & SON: PHILADELPHIA, 1979 A REVIEW.a
  172953. GABRIEL WEATHERHEAD
  172954. 11233
  172955. 12242N
  172956. 2/28/96
  172957. STOIANOVA IVANOVA, B. COMPOSITION OF BULGARIAN ROSE FLOWER CONCRETE
  172958. THE STRUCTURE AND BIOGENESIS OF ITS COMPONENTS. RECENT DEVELOPMENTS IN THE CHEMISTRY OF NATURAL CARBON COMPOUNDS (VOL. 9, R. BOGNAR, V. BRUCKNER, AND CS. SZANTAY, EDS.), HEYDEN & SON: PHILADELPHIA, 1979 A REVIEW.
  172959. GABRIEL WEATHERHEAD
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  172961. 12243N
  172962. 2/28/96V
  172963. MORI, K. SYNTHETIC CHEMISTRY OF INSECT PHEROMONES AND JUVENILE HORMONES. RECENT DEVELOPMENTS IN THE CHEMISTRY OF NATURAL CARBON COMPOUNDS (VOL. 9, R. BOGNAR, V. BRUCKNER, AND CS. SZANTAY, EDS.), HEYDEN & SON: PHILADELPHIA, 1979 A REVIEW.a
  172964. GABRIEL WEATHERHEAD
  172965. 11235
  172966. 12244N
  172967. 2/28/96
  172968. RAMAGE, R. ORGANOPHOSPHORUS REAGENTS IN THE SYNTHESIS OF PEPTIDES. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172969. GABRIEL WEATHERHEAD
  172970. 11236
  172971. 12245N
  172972. 2/28/96V
  172973. BURGER, K. PENTACOORDINATE PHOSPHORANES IN SYNTHESIS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172974. GABRIEL WEATHERHEAD
  172975. 11237
  172976. 12246N
  172977. 2/28/96V
  172978. MACKIE, R. K. FUNCTIONAL GROUP CONVERSIONS USING PHOSPHORUS(III) REAGENTS WITH HALIDES AND HALOGENS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172979. GABRIEL WEATHERHEAD
  172980. 11238
  172981. 12247N
  172982. 2/28/96V
  172983. APPEL, R.; HALSTENBERG, M. FUNCTIONAL GROUP CONVERSIONS USING PHOSPHORUS(III) REAGENTS AND POLYHALOGENOALKANES. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172984. GABRIEL WEATHERHEAD
  172985. 11239
  172986. 12248N
  172987. 2/28/96V
  172988. MACKIE, R. K. DESULPHURIZATION VIA PHOSPHORUS(III) REAGENTS: GENERAL FUNCTIONAL GROUP CONVERSIONS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172989. GABRIEL WEATHERHEAD
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  172992. 2/28/96V
  172993. ROWLEY, A. G. DEOXYGENATION USING PHOSPHORUS(III) REAGENTS 1: GENERAL FUNCTIONAL GROUP CONVERSIONS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172994. GABRIEL WEATHERHEAD
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  172996. 12250N
  172997. 2/28/96V
  172998. CADOGAN, J. I. G. DEOXYGENATION VIA PHOSPHORUS(III) REAGENTS 1: HETEROCYCLIC SYNTHESIS USING AROMATIC NITRO COMPOUNDS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  172999. GABRIEL WEATHERHEAD
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  173001. 12251N
  173002. 2/28/96
  173003. ZBIRAL, E. TRANSFORMATIONS VIA PHOSPHORUS STABILIZED ANIONS 4: HETEROCYCLIC SYNTHESIS VIA ALKYLIDENOPHOSPHORANES, IMINOPHOSPHORANES AND VINYLPHOSPHONIUM SALTS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.
  173004. GABRIEL WEATHERHEAD
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  173006. 12252N
  173007. 2/28/96V
  173008. SMITH, D. J. H. TRANSFORMATIONS VIA PHOSPHORUS STABILIZED ANIONS 3: REACTIONS WITH ELECTROPHILES OTHER THAN ALDEHYDES AND KETONES. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173009. GABRIEL WEATHERHEAD
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  173011. 12253N
  173012. 2/28/96V
  173013. WALKER, B. J. TRANSFORMATIONS VIA PHOSPHORUS STABILIZED ANIONS 2: PO ACTIVATED OLEFINATION. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173014. GABRIEL WEATHERHEAD
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  173016. 12254N
  173017. 2/28/96
  173018. GOSNEY, I.; ROWLEY, A. G. TRANSFORMATIONS VIA PHOSPHORUS STABILIZED ANIONS 1: STEREOSELECTIVE SYNTHESES OF ALKENES VIA THE WITTIG REACTIONS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173019. GABRIEL WEATHERHEAD
  173020. 11246
  173021. 12255N
  173022. 2/28/96V
  173023. CADOGAN, J. I. G. TYPES OF ORGANOPHOSPHORUS REAGENTS AND THEIR KEY REACTIONS. ORGANOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS J. I. G. CADOGEN, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173024. GABRIEL WEATHERHEAD
  173025. 11247
  173026. 12256N
  173027. 2/28/96
  173028. 8HULSHOF, L. A.; WYNBERG, H. ON THE VANISHING OPTICAL ACTIVITY OF QUATERNARY HYDROCARBONS, P 373. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173029. GABRIEL WEATHERHEAD
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  173033. REES, C. W. THE CHEMISTRY OF BENZAZETES, P 356. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173034. GABRIEL WEATHERHEAD
  173035. 11249
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  173038. @PADWA, A.; CARLSEN, PER H. J.; KAMIGATA, N. PHOTOCHEMICAL CONSTRUCTION OF HETEROCYCLIC COMPOUNDS, P 341. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173039. GABRIEL WEATHERHEAD
  173040. 11250
  173041. 12259N
  173042. 2/28/96
  173043.  MAGARAJAN, K. DIBENZOXAZEPINES
  173044. CHEMISTRY AND BIOLOGICAL ACTIVITY, P 317. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173045. GABRIEL WEATHERHEAD
  173046. 11251
  173047. 12260N
  173048. 2/28/96
  173049. QMITRA, R. B.; KULKARNI, G. H.; SHIRWAIKAR, G. S.; JAGTAP, R. S. CYCLOADDITION REACTIONS OF TRIHETEROATOMIC AZOLES, P 309. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173050. GABRIEL WEATHERHEAD
  173051. 11252
  173052. 12261N
  173053. 2/28/96
  173054. `KATRITZKY, A. R.; DENNIS, N. RECENT PROGRESS IN THE CYCLOADDITION REACTIONS OF 3 0XIDOPYRIDMIUM BETAINES AND ANALOGOUS COMPOUNDS, P 290. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173055. GABRIEL WEATHERHEAD
  173056. 11253
  173057. 12262N
  173058. 2/28/96
  173059. IDDON, B. RECENT ADVANCES IN THE SYNTHESIS OF BENZO[B]THIOPHENS, P 250. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173060. GABRIEL WEATHERHEAD
  173061. 11254
  173062. 12263N
  173063. 2/28/96
  173064. (HUGHES, A. N. RECENT DEVELOPMENTS IN PHOSPHOLE AND PHOSPHINDOLE CHEMISTRY, P 216. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V.N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173065. GABRIEL WEATHERHEAD
  173066. 11255
  173067. 12264N
  173068. 2/28/96
  173069. 2DEUCHERT, K.; HUNIG, S. SOME 3,5 BIFUNCTIONAL PYRIDINES AND RELATED PYRIDINOPHANES, P 202. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173070. GABRIEL WEATHERHEAD
  173071. 11256
  173072. 12265N
  173073. 2/28/96
  173074. HASSNER, A.; ALEXANIAN, V. RECENT ASPECTS OF AZIRINE CHEMISTRY, P 178. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173075. GABRIEL WEATHERHEAD
  173076. 11257
  173077. 12266N
  173078. 2/28/96
  173079. ABRONIN, I. A.; BALEN KII, L. I., GOL'DFARB, YA. L. ELECTROPHILIC SUBSTITUTION IN THE SERIES OF FIVE MEMBERED HETEROAROMATIC COMPOUNDS: A QUANTUM CHEMICAL STUDY, P 154. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173080. GABRIEL WEATHERHEAD
  173081. 11258
  173082. 12267N
  173083. 2/28/96
  173084. )GOGTE, V. N.; MODAK, H. M. THIIRANIUM SALTS/IONS AS REACTION INTERMEDIATES P 142. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173085. GABRIEL WEATHERHEAD
  173086. 11259
  173087. 12268N
  173088. 2/28/96
  173089. 2DITTMER, D. C. CHEMISTRY OF THIACYCLOBUTENES (THIETES) AND THEIR VALENCE TAUTOMERS, P 130. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173090. GABRIEL WEATHERHEAD
  173091. 11260
  173092. 12269N
  173093. 2/28/96
  173094. {TARBURTON, P.; KINGSBURY, C. A.; CROMWELL N. H. STEREOSTRUCTURAL INVESTIGATIONS OF TRANS  AND CIS 1 ALKYL 2 ARYL(ALKYL) 3 CARBOAZIRIDINES BY 1H AND 13C NMR, P 112. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173095. GABRIEL WEATHERHEAD
  173096. 11261
  173097. 12270N
  173098. 2/28/96
  173099. #BALABAN, A. T. THE PYRYLIUM CATION AS A SYNTHON IN ORGANIC CHEMISTRY, P 79. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173100. GABRIEL WEATHERHEAD
  173101. 11262
  173102. 12271N
  173103. 2/28/96
  173104.  PEACH, J. M.; BAILERY, A. S. THE REACTIONS OF AZIDES WITH INDOLES, P 56. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173105. GABRIEL WEATHERHEAD
  173106. 11263
  173107. 12272N
  173108. 2/28/96
  173109. .AYYANGAR, N. R.; LUGADE, A. G. NAPHTHINDOLIZINE AND NAPHTHIMIDAZOPYRIDINEDIONES, P 34. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173110. GABRIEL WEATHERHEAD
  173111. 11264
  173112. 12273N
  173113. 2/28/96
  173114. (ACHESON, R. M. THE CHEMISTRY, REACTIONS AND PROPERTIES OF L HYDROXYINDOLES, P 1. NEW TRENDS IN HETEROCYCLIC CHEMISTRY (STUDIES IN ORGANIC CHEMISTRY 3, R. B. MITRA, N. R. AYYANGAR, V. N. GOGTE, R. M. ACHESON, AND N. CROMWELL, EDS.), ELSEVIER SCIENTIFIC PUBLISHING COMPANY: NEW YORK, 1979 A REVIEW.
  173115. GABRIEL WEATHERHEAD
  173116. 11265
  173117. 12274N
  173118. 2/28/96V
  173119. MULLEN, A. RING CLOSURE REACTIONS WITH CARBON MONOXIDE. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173120. GABRIEL WEATHERHEAD
  173121. 11266
  173122. 12275N
  173123. 2/28/96VxBAHRMANN, H. KOCH REACTIONS. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173124. GABRIEL WEATHERHEAD
  173125. 11267
  173126. 12276N
  173127. 2/28/96V
  173128. FROHNING, C. D. FISCHER TROPSCH SYNTHESIS. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173129. GABRIEL WEATHERHEAD
  173130. 11268
  173131. 12277N
  173132. 2/28/96
  173133. MULLEN, A. CARBONYLATIONS CATALYZED BY METAL CARBONYLS/REPPE REACTION. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173134. GABRIEL WEATHERHEAD
  173135. 11269
  173136. 12278N
  173137. 2/28/96V
  173138. BAHRMAN, H.; CORNILS, B. HOMOLOGATION OF ALCOHOLS. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173139. GABRIEL WEATHERHEAD
  173140. 11270
  173141. 12279N
  173142. 2/28/96VyCORNILS, B. HYDROFORMYLATION. NEW SYNTHESES WITH CARBON MONOXIDE J. FALBE, ED., SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  173143. GABRIEL WEATHERHEAD
  173144. 11271
  173145. 12280N
  173146. 2/28/96V
  173147. ROBERTS, B. P. THE CHEMISTRY OF PHOSPHORANYL RADICALS. ADVANCES IN FREE RADICAL CHEMISTRY (VOL. 6, G. H. WILLIAMS, ED.), HEYDEN & SON: PHILADELPHIA, 1980 A REVIEW.a
  173148. GABRIEL WEATHERHEAD
  173149. 11272
  173150. 12281N
  173151. 2/28/96
  173152. CADOGEN, J. I. G. THE MECHANISTIC ROLE OF RADICALS, IONS AND ARYNES IN REACTIONS OF ACYLARYLNITROSAMINES. ADVANCES IN FREE RADICAL CHEMISTRY (VOL. 6, G. H. WILLIAMS, ED.), HEYDEN & SON: PHILADELPHIA, 1980 A REVIEW.a
  173153. GABRIEL WEATHERHEAD
  173154. 11273
  173155. 12282N
  173156. 2/28/96V
  173157. TEDDER, J. M.; WALTON, J. C. THE HALOGENATION OF THE CYCLOALKANE AND THEIR DERIVATIVES. ADVANCES IN FREE RADICAL CHEMISTRY (VOL. 6, G. H. WILLIAMS, ED.), HEYDEN & SON: PHILADELPHIA, 1980 A REVIEW.a
  173158. GABRIEL WEATHERHEAD
  173159. 11274
  173160. 12283N
  173161. 2/28/96V
  173162. MINISCI, F.; CITTERIO, A. POLAR EFFECTS IN FREE RADICAL REACTIONS IN SYNTHETIC CHEMISTRY. ADVANCES IN FREE RADICAL CHEMISTRY (VOL. 6, G. H. WILLIAMS, ED.), HEYDEN & SON: PHILADELPHIA, 1980 A REVIEW.a
  173163. GABRIEL WEATHERHEAD
  173164. 11275
  173165. 12284N
  173166. 2/28/96
  173167. FREIDLINA, R. KH.; TERENT'EV, A. B. REARRANGEMENT OF SHORT LIVED RADICALS IN THE LIQUID PHASE. ADVANCES IN FREE RADICAL CHEMISTRY (VOL. 6, G. H. WILLIAMS, ED.), HEYDEN & SON: PHILADELPHIA, 1980 A REVIEW.a
  173168. GABRIEL WEATHERHEAD
  173169. 11276
  173170. 12285N
  173171. 2/28/96V
  173172. FODOR G.; NAGUBANDI, S. CORRELATION OF THE VON BRAUN, RITTER, BISCHLER NAPIERALSKI, BECKMANN AND SCHMIDT REACTIONS VIA NITRILIUM SALT INTERMEDIATES. 1980, 36,1279. TETRAHEDRON A REVIEW.a
  173173. GABRIEL WEATHERHEAD
  173174. 11277
  173175. 12286N
  173176. 2/28/96VkCANE, D. E. THE STEREOCHEMISTRY OF ALLYLIC PYRO  PHOSPHATE METABOLISM. 1980, 36,1109. TETRAHEDRON A REVIEW.a
  173177. GABRIEL WEATHERHEAD
  173178. 11278
  173179. 12287N
  173180. 2/28/96VkMCKERVEY, M. A. SYNTHETIC APPROACHES TO LARGE DIAMONDOID HYDROCARBONS. 1980, 36, 971. TETRAHEDRON A REVIEW.a
  173181. GABRIEL WEATHERHEAD
  173182. 11279
  173183. 12288N
  173184. 2/28/96VzADAM, W.; BALCI, M. CYCLIC POLYEPOXIDES. SYNTHETIC STRUCTURAL AND BIOLOGICAL ASPECTS. 1980, 36, 833. TETRAHEDRON A REVIEW.
  173185. GABRIEL WEATHERHEAD
  173186. 11280
  173187. 12289N
  173188. 2/28/96V
  173189. TEDDER, J. M.; WALTON, J. C. THE IMPORTANCE OF POLARITY AND STERIC EFFECTS IN DETERMINMG THE RATE AND ORIENTATION OF FREE RADICAL ADDITION TO OLEFINS. RULES FOR DETERMINING THE RATE NND PREFERRED ORIENTATION. 1980, 36, 701. TETRAHEDRON A REVIEW.a
  173190. GABRIEL WEATHERHEAD
  173191. 11281
  173192. 12290N
  173193. 2/28/96V
  173194. KATRITZKY, A. R. CONVERSIONS OF PRIMARY AMINO GROUPS INTO OTHER FUNCTIONALITY MEDIATED BY PYRYLIUM CATIONS. 1980, 36, 679. TETRAHEDRON A REVIEW.a
  173195. GABRIEL WEATHERHEAD
  173196. 11282
  173197. 12291N
  173198. 2/28/96VDSONNET, P. E. OLEFIN INVERSION. 1980, 36, 557. TETRAHEDRON A REVIEW.a
  173199. GABRIEL WEATHERHEAD
  173200. 11283
  173201. 12292N
  173202. 2/28/96V
  173203. BRADSHAW, J. S.; STOTT, P. E. PREPARATION OF DERIVATIVES AND ANALOGS OF THE MACROCYCLIC OLIGOMERS OF ETHYLENE OXIDE (CROWN COMPOUNDS). 1980, 36, 461. TETRAHEDRON A REVIEW.a
  173204. GABRIEL WEATHERHEAD
  173205. 11284
  173206. 12293N
  173207. 2/28/96
  173208. VqMARTIN, S. F. METHODOLOGY FOR THE CONSTRUCTION OF QUATERNARY CARBON CENTERS. 1980, 36, 419. TETRAHEDRON A REVIEW.a
  173209. GABRIEL WEATHERHEAD
  173210. 11285
  173211. 12294N
  173212. 2/28/96VLBALLY, T.; MASAMUNE, S. CYCLOBUTADIENE. 1980, 36, 343. TETRAHEDRON A REVIEW.a
  173213. GABRIEL WEATHERHEAD
  173214. 11286
  173215. 12295N
  173216. 2/28/96VRHUCHE, M. ALPHA AIIENIC KETONES (IN FRENCH). 1980, 36, 331.  TETRAHEDRON A REVIEW.a
  173217. GABRIEL WEATHERHEAD
  173218. 11287
  173219. 12296N
  173220. 2/28/96V
  173221. FUSCO, R.; FANNICOLO, F. N N BOND CLEAVAGE AND REARRANGEMENTS OF ARYLHYDRAZONES AND ARYLHYDRAZIDES
  173222. RECENT DEVELOPMENTS. 1980, 36,161. TETRAHEDRON A REVIEW.a
  173223. GABRIEL WEATHERHEAD
  173224. 11288
  173225. 12297N
  173226. 2/28/96V
  173227. BARTLETT, P. A. STEREOCONTROL IN THE SYNTHESIS OF ACYCLIC SYSTEMS: APPLICATIONS TO NATURAL PRODUCT SYNTHESIS. 1980, 36, 2. TETRAHEDRON A REVIEW.a
  173228. GABRIEL WEATHERHEAD
  173229. 11289
  173230. 12298N
  173231. 2/28/96V]MUSSO, H. THE PIGMENTS OF FLY AGARIC, AMANITA MUSCARIA. 1979, 35, 2843. TETRAHEDRON A REVIEW.
  173232. GABRIEL WEATHERHEAD
  173233. 11290
  173234. 12299N
  173235. 2/28/96VlAPSIMON, J. W., SEGUIN, R. P. RECENT ADVANCES IN ASYMMETRIC SYNTHESIS. 1979, 35, 2797. TETRAHEDRON A REVIEW.a
  173236. GABRIEL WEATHERHEAD
  173237. 11291
  173238. 12300N
  173239. 2/28/96VSPINDER, A. R. THE HYDROGENOLYSIS OF ORGANIC HALIDES. 1980, 425. SYNTHESIS A REVIEW.a
  173240. GABRIEL WEATHERHEAD
  173241. 11292
  173242. 12301N
  173243. 2/28/96V
  173244. YAKOBSON, G. G.; FURIN, G. G. ANTIMONY PENTAHALIDES AS CATALYSIS OF FRIEDEL CRAFTS TYPE REACTIONS. 1980, 345. SYNTHESIS A REVIEW.a
  173245. GABRIEL WEATHERHEAD
  173246. 11293
  173247. 12302N
  173248. 2/28/96VsFISCHER, R. H., WEITZ, H. M. PREPARATION AND REACTIONS OF CYCLIC ALPHA NITROKETONES. 1980, 261. SYNTHESIS A REVIEW.a
  173249. GABRIEL WEATHERHEAD
  173250. 11294
  173251. 12303N
  173252. 2/28/96VyWAGNER JAUREGG, T. THERMAL AND PHOTOCHEMICAL ADDITION OF DIENOPHILES TO ARENES (IN GERMAN). 1980,165. SYNTHESIS A REVIEW.a
  173253. GABRIEL WEATHERHEAD
  173254. 11295
  173255. 12304N
  173256. 2/28/96
  173257. VwGORBATENKO, V. I.; SAMARAI, L. I. SYNTHESIS AND REACTIONS OF ALPHA HALOALKYL ISOCYANATES. 1980, 85. SYNTHESIS A REVIEW.a
  173258. GABRIEL WEATHERHEAD
  173259. 11296
  173260. 12305N
  173261. 2/28/96VcPILLAI, V. N. R. PHOTOREMOVABLE PROTECTING GROUPS IN ORGANIC SYNTHESIS. 1980,1. SYNTHESIS A REVIEW.a
  173262. GABRIEL WEATHERHEAD
  173263. 11297
  173264. 12306N
  173265. 2/28/96V
  173266. BERLIN, A. A.; SHERLE, A. I. THE SYNTHESIS AND PROPERTIES OF POLYMERIC AZAPORPHIN COMPOUNDS. 1979, 48,1125. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173267. GABRIEL WEATHERHEAD
  173268. 11298
  173269. 12307N
  173270. 2/28/96V
  173271. MORKOVNIK, A. F.; OKHLOBYSTIN, O. YU. INORGANIC RADICAL IONS AND THEIR ORGANIC REACTIONS. 1979, 48,1055. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173272. GABRIEL WEATHERHEAD
  173273. 11299
  173274. 12308N
  173275. 2/28/96V
  173276. FRUNZE, T. M., KURASHEV, V. V., KOTEL'NIKOV, V. A.VOLKOVA, T. V. ACTIVATORS OF THE ANIONIC POLYMERIZATION OF LACTAMS. 1979, 48, 991. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173277. GABRIEL WEATHERHEAD
  173278. 11300
  173279. 12309N
  173280. 2/28/96
  173281. VORONKOV, M. G.; CHERNOV, N. F. MIXED ORGANIC DERIVATIVES OF MERCURY AND SILICON. 1979, 48, 964. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173282. GABRIEL WEATHERHEAD
  173283. 11301
  173284. 12310N
  173285. 2/28/96V
  173286. SLADKOV, A. M.; GOL'DING, I. R. REACTIONS OF COPPER AND SILVER ORGANOACETYLIDES. 1979, 48, 868. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173287. GABRIEL WEATHERHEAD
  173288. 11302
  173289. 12311N
  173290. 2/28/96V
  173291. FREIDLINA, R. KH.; TERENT'EV, A. B. THE ISOMERIZATION OF UNSTABLE ORGANOELEMENTAL RADICALS IN LIQUID PHASE REACTIONS. 1979, 48, 828. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173292. GABRIEL WEATHERHEAD
  173293. 11303
  173294. 12312N
  173295. 2/28/96VmKABACHNIK, M. I. PROGRESS IN THE THEORY OF ACIDS AND BASES. 1979, 48, 814. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173296. GABRIEL WEATHERHEAD
  173297. 11304
  173298. 12313N
  173299. 2/28/96V
  173300. LOBACH, M. I.; KORMER, V. A. INSERTION OF DIENE HYDROCARBONS IN TRANSITION METAL LIGAND BONDS. 1979, 48, 758. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173301. GABRIEL WEATHERHEAD
  173302. 11305
  173303. 12314
  173304. 2/28/96V
  173305. ZUBAREV, V. E.; BELEVSKII, V. N.; BUGAENKO, L. T. THE USE OF SPIN TRAPPING IN THE STUDY OF THE MECHANISMS OF RADICAL PROCESSES. 1979, 48, 729. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173306. GABRIEL WEATHERHEAD
  173307. 11306
  173308. 12315N
  173309. 2/28/96V
  173310. NASIROVA, R. M.; MURAV'EVA, L. S.; MUSHINA, E. A.; KRENTSEL', B. A. THE REACTIVITY OF AROMATIC DIALKENYL COMPOUNDS IN POLYMERIZATION REACTIONS. 1979, 48, 692. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173311. GABRIEL WEATHERHEAD
  173312. 11307
  173313. 12316N
  173314. 2/28/96VuKOPELEVICH, V. M. MEDICINAL DRUGS BASED ON GAMMA AMINOBUTYRIC ACID. 1979, 48, 679. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173315. GABRIEL WEATHERHEAD
  173316. 11308
  173317. 12317N
  173318. 2/28/96V
  173319. SYTINSKII, I. A.; SOLDATENKOV, A. T. THE CONFORMATION OF GAMMA AMINOBUTYRIC ACID AND ITS ANALOGUES. 1979, 48, 669. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173320. GABRIEL WEATHERHEAD
  173321. 11309
  173322. 12318N
  173323. 2/28/96
  173324. ANDRIANOV, K. A.; SOUCEK, J., KHANANASHVILI, L. M. THE HYDRIDE ADDITION OF ORGANOHYDROSILOXANES TO COMPOUNDS WITH A MULTIPLE CARBON CARBON BOND. 1979, 48, 657. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173325. GABRIEL WEATHERHEAD
  173326. 11310
  173327. 12319N
  173328. 2/28/96V
  173329. SOLOV'EV, A. A.; KADENTSEV, V. I.; CHIZHOV, O. S. MASS SPECTROMETRY WITH CHEMICAL IONIZATION. 1979, 48, 631. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  173330. GABRIEL WEATHERHEAD
  173331. 11311
  173332. 12320N
  173333. 2/28/96V
  173334. CHILDS, R. F. THE PHOTOCHEMISTRY OF PROTONATED UNSATURATED CARBONYL COMPOUNDS. 1980, 3, 285. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  173335. GABRIEL WEATHERHEAD
  173336. 11312
  173337. 12321N
  173338. 2/28/96
  173339. SANTUS, R., BAZIN, M.; AUBAILLY, M. NATURE, IDENTIFICATION AND PROPERTIES OF INTERMEDIATES PRODUCED BY UV EXCITATION OF INDOLE DERIVATIVES AT LOW AND ROOM TEMPERATURES. SOME APPLICATIONS TO TRYPTOPHAN CONTAINING PROTEINS. 1980, 3, 231. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.
  173340. GABRIEL WEATHERHEAD
  173341. 11313
  173342. 12322N
  173343. 2/28/96V
  173344. KASAI, T.; LARSEN P. O. CHEMISTRY AND BIOCHEMISTRY OF GAMMA GIUTAMYL DERIVATIVES FROM PLANTS INCLUDING MUSHROOMS (BASIDIOMYCETES). 1980, 39,173. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173345. GABRIEL WEATHERHEAD
  173346. 11314
  173347. 12323N
  173348. 2/28/96V
  173349. LIAAEN JENSEN, S. STEREOCHEMISTRY OF NATURALLY OCCURRING CAROTENOIDS. 1980 39,123. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173350. GABRIEL WEATHERHEAD
  173351. 11315
  173352. 12324N
  173353. 2/28/96V
  173354. JONES, H.; RASMUSSON, G. H. RECENT ADVANCES IN THE BIOLOGY AND CHEMISTRY OF VITAMIN D. 1980, 39, 63. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173355. GABRIEL WEATHERHEAD
  173356. 11316
  173357. 12325N
  173358. 2/28/96V
  173359. FRASER REID, B.; ANDERSON, R. C. CARBOHYDRATE DERIVATIVES IN THE ASYMMETRIC SYNTHESIS OF NATURAL PRODUCTS. 1980, 39, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173360. GABRIEL WEATHERHEAD
  173361. 11317
  173362. 12326N
  173363. 2/28/96
  173364. FISCHER, N. H.; OLIVIER, E. J.; FISCHER, H. D. THE BIOGENESIS AND CHEMISTRY OF SESQUITERPENE LACTONES. 1979, 38, 47. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173365. GABRIEL WEATHERHEAD
  173366. 11318
  173367. 12327N
  173368. 2/28/96VtFRANCK, R. W. THE MITOMYCIN ANTIBIOTICS. 1979, 38,1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  173369. GABRIEL WEATHERHEAD
  173370. 11319
  173371. 12328N
  173372. 2/28/96V
  173373. SCHWARTZ, J.; LABINGER, J. A. PATTERNS IN ORGANOMETALLIC CHEMISTRY WITH APPLICATION IN ORGANIC SYNTHESIS. 1980, JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  173374. GABRIEL WEATHERHEAD
  173375. 11320
  173376. 12329N
  173377. 2/28/96V{WEST, R.; BARTON, T. J. ORGANOSILICON CHEMISTRY. PARTS I AND II. 1980, 57,165, 334. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  173378. GABRIEL WEATHERHEAD
  173379. 11321
  173380. 12330N
  173381. 2/28/96V
  173382. MCKINNEY, M. A.; HAWORTH, D. T. SIGMA BONDED CYCLOPOLYENYL METAL COMPLEXES. 1980, 57,110. JOURNAL OF CHEMICAL EDUCATION A REVIEW.a
  173383. GABRIEL WEATHERHEAD
  173384. 11322
  173385. 12331N
  173386. 2/28/96V}IKEDA, M.; TAMURA, Y. 3 HALOINDOLENINES
  173387. VERSATILE INTERMEDIATES IN THE INDOLE CHEMISTRY. 1980,14, 867. HETEROCYCLES A REVIEW.a
  173388. GABRIEL WEATHERHEAD
  173389. 11323
  173390. 12332N
  173391. 2/28/96VhTRALDI, P.; VETTORI, U.; CLERICI, A. MASS SPECTROMETRY OF OXAZOLES. 1980,14, 847. HETEROCYCLES A REVIEW.a
  173392. GABRIEL WEATHERHEAD
  173393. 11324
  173394. 12333N
  173395. 2/28/96VdBOSCH, J.; BONJOCH, J. SYNTHESIS OF 2 AZABICYCLO[3.3.1]NONANES. 1980,14, 505. HETEROCYCLES A REVIEW.a
  173396. GABRIEL WEATHERHEAD
  173397. 11325
  173398. 12334N
  173399. 2/28/96V
  173400. BROPHY, J. J.; CAVILL, G. W. K. NATURALLY OCCURRING PYRAZINES AND THEIR MASS SPECTROMETRIC CHARACTERIZATION. 1980, 14, 477. HETEROCYCLES A REVIEW.a
  173401. GABRIEL WEATHERHEAD
  173402. 11326
  173403. 12335N
  173404. 2/28/96VvSEOANE, C.; SOTO, J. L.; QUINTEIRO, M. SYNTHETIC APPROACHES TO THE 4H PYRAN RING. 1980,14, 337. HETEROCYCLES A REVIEW.a
  173405. GABRIEL WEATHERHEAD
  173406. 11327
  173407. 12336N
  173408. 2/28/96
  173409. CASSELS, B. K.; SHAMMA, M. STEREOSTRUCTURE AND SPECIFIC ROTATION FOR THE BISBENZYLISOQUINOLINES. 1980,14, 211. HETEROCYCLES A REVIEW.a
  173410. GABRIEL WEATHERHEAD
  173411. 11328
  173412. 12337N
  173413. 2/28/96VwPANDEY, G. D.; TIWARI, K. P. RECENT ADVANCES IN THE CHEMISTRY OF BERBINE ALKALOIDS. 1980,14, 59. HETEROCYCLES A REVIEW.a
  173414. GABRIEL WEATHERHEAD
  173415. 11329
  173416. 12338N
  173417. 2/28/96VRSASAKI, T. NEW TYPED HETEROCYCLIC COMPOUNDS. 1979, 13, 531. HETEROCYCLES A REVIEW.a
  173418. GABRIEL WEATHERHEAD
  173419. 11330
  173420. 12339N
  173421. 2/28/96VxKAMETANI, T.; IHARA, M. CHEMICAL AND BIOCHEMICAL ASPECTS OF ISOQUINOLINE ALKALOIDS. 1979,13, 497. HETEROCYCLES A REVIEW.a
  173422. GABRIEL WEATHERHEAD
  173423. 11331
  173424. 12340N
  173425. 2/28/96V
  173426. NAKAGAWA, S., NAITO, T.; KAWAGUCHI, H. STRUCTURES OF BU 2312 A AND B, NEW ANTI ANAEROBIC ANTIBIOTICS AND SYNTHESES OF THEIR ANALOGS. 1979,13, 477. HETEROCYCLES A REVIEW.a
  173427. GABRIEL WEATHERHEAD
  173428. 11332
  173429. 12341N
  173430. 2/28/96
  173431. TANAKA, W.; TAKITA, T. PEPLEOMYCIN, THE SECOND GENERATION BLEOMYCIN CHEMICALLY DERIVED FROM BLEOMYCIN A2. 1979, 13, 469. HETEROCYCLES A REVIEW.a
  173432. GABRIEL WEATHERHEAD
  173433. 11333
  173434. 12342N
  173435. 2/28/96VwTAKAHASHI, K.; KAMETANI, T. SYNTHETIC STUDIES ON MITOMYCINS AND RELATED COMPOUNDS. 1979,13, 411. HETEROCYCLES A REVIEW.a
  173436. GABRIEL WEATHERHEAD
  173437. 11334
  173438. 12343N
  173439. 2/28/96VoCONTRERAS, F. G.; LORA TAMAYO, M. TRANSFORMATIONS ON DIAZAQUINONE ADDUCTS. 1979,13, 389. HETEROCYCLES A REVIEW.a
  173440. GABRIEL WEATHERHEAD
  173441. 11335
  173442. 12344N
  173443. 2/28/96VoNAKANO, K I. SYNTHESIS AND BIOLOGICAL ACTIVITIES OF MITOMYCIN DERIVATIVES. 1979,13, 373. HETEROCYCLES A REVIEW.a
  173444. GABRIEL WEATHERHEAD
  173445. 11336
  173446. 12345N
  173447. 2/28/96V
  173448. TERAHARA, A.; HANEISHI, T.; ARAI, M. METHYLENOMYCIN A, AN ANTIBIOTIC WITH CHEMICALLY VERSATILE FUNCTIONS. 1979, 13, 353. HETEROCYCLES A REVIEW.a
  173449. GABRIEL WEATHERHEAD
  173450. 11337
  173451. 12346N
  173452. 2/28/96
  173453. ISONO, K.; SUZUKI, S. THE POLYOXINS: PYRIMIDINE NUCLEOSIDE PEPTIDE ANTIBIOTICS INHIBITING FUNGAL CELL WALL BIOSYNTHESIS. 1979,13, 333. HETEROCYCLES A REVIEW.a
  173454. GABRIEL WEATHERHEAD
  173455. 11338
  173456. 12347N
  173457. 2/28/96VhUMEZAWA, H. RECENT CHEMICAL STUDIES OF BIOACTIVE MICROBIAL PRODUCTS. 1979,13, 23. HETEROCYCLES A REVIEW.a
  173458. GABRIEL WEATHERHEAD
  173459. 11339
  173460. 12348N
  173461. 2/28/96V
  173462. HATHWAY, D. E. THE IMPORTANCE OF (NON ENZYMIC) CHEMICAL REACTION PROCESSES TO THE FATE OF FOREIGN COMPOUNDS IN MAMMALS. 1980, 9, 63. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173463. GABRIEL WEATHERHEAD
  173464. 11340
  173465. 12349N
  173466. 2/28/96V
  173467. FUNK, R. L.;VOLLHERDT, K. P. C. THERMAL, PHOTOCHEMICAL AND TRANSITION METAL MEDIATED ROUTES TO STEROIDS BY INTRAMOLECULAR DIELS ALDER REACTIONS OF O XYLYLENES (OQUINODIMETHANES). 1980, 9, 41. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173468. GABRIEL WEATHERHEAD
  173469. 11341
  173470. 12350N
  173471. 2/28/96
  173472. MALOWSKY, E., JR. THE SYNTHESIS, STRUCTURE, AND VIBRATIONAL SPECTRA OF ORGANOMETHYL COMPOUNDS. 1980, 9, 25. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173473. GABRIEL WEATHERHEAD
  173474. 11342
  173475. 12351N
  173476. 2/28/96V
  173477. DUNKIN, I. R. THE MATRIX ISOLATION TECHNIQUE AND ITS APPLICATION TO ORGANIC CHEMISTRY. 1980, 9,1. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173478. GABRIEL WEATHERHEAD
  173479. 11343
  173480. 12352N
  173481. 2/28/96V
  173482. GARSON, M. J.; STAUNTON, J. NEW NMR METHODS FOR TRACING THE FATE OF HYDROGEN IN BIOSYNTHESIS. 1979, 8, 539. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173483. GABRIEL WEATHERHEAD
  173484. 11344
  173485. 12353N
  173486. 2/28/96VbTYMAN J. H. P. NON ISOPRENOID LONG CHAIN PHENOLS. 1979, 8, 499. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173487. GABRIEL WEATHERHEAD
  173488. 11345
  173489. 12354N
  173490. 2/28/96VkOVERTON, K. H. STEREOCHEMICAL CHOICE IN ENZYMIC REACTIONS. 1979, 8, 447. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173491. GABRIEL WEATHERHEAD
  173492. 11346
  173493. 12355N
  173494. 2/28/96
  173495. VwAMBROZ, H. B.; KEMP T. J. ARYL CATIONS
  173496. NEW LIGHT ON OLD INTERMEDIATES. 1979, 8, 353. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173497. GABRIEL WEATHERHEAD
  173498. 11347
  173499. 12356N
  173500. 2/28/96V
  173501. GILLESPIE, R. J. RING, CAGE, AND CLUSTER COMPOUNDS OF THE MAIN GROUP ELEMENTS. 1979, 8, 315. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  173502. GABRIEL WEATHERHEAD
  173503. 11348
  173504. 12357N
  173505. 2/28/96VsSCHRODER, M. OSMIUM TETRAOXIDE CIS HYDROXYLATION OF UNSATURATED SUBSTRATES. 1980, 2,187. CHEMICAL REVIEWS A REVIEW.a
  173506. GABRIEL WEATHERHEAD
  173507. 11349
  173508. 12358N
  173509. 2/28/96VwBENSON, G. A., SPILLANE, W. J. SULFAMIC ACID AND ITS N SUBSTITUTED DERIVATIVES. 1980, 2,151. CHEMICAL REVIEWS A REVIEW.a
  173510. GABRIEL WEATHERHEAD
  173511. 11350
  173512. 12359N
  173513. 2/28/96V}ENGEL, P. S. MECHANISMS OF THE THERMAL AND PHOTOCHEMICAL DECOMPOSITION OF AZOALKANES. 1980, 2, 99. CHEMICAL REVIEWS A REVIEW.a
  173514. GABRIEL WEATHERHEAD
  173515. 11351
  173516. 12360N
  173517. 2/28/96
  173518. VlBRIEGER, G.; BENNETT, J. N. THE INTRAMOLECULAR DIELS ALDER REACTIONS. 1980,1, 63. CHEMICAL REVIEWS A REVIEW.a
  173519. GABRIEL WEATHERHEAD
  173520. 11352
  173521. 12361N
  173522. 2/28/96V
  173523. RUCHARDT C., BECKHAUS, H. D. TOWARDS AN UNDERSTANDING OF THE CARBON CARBON BOND. 1980, 6, 429. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173524. GABRIEL WEATHERHEAD
  173525. 11353
  173526. 12362N
  173527. 2/28/96V
  173528. BINSCH, G., KESSLER, H. THE KINETIC AND MECHANISTIC EVALUATION OF NMR SPECTRA. 1980, 6,111. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173529. GABRIEL WEATHERHEAD
  173530. 11354
  173531. 12363N
  173532. 2/28/96V
  173533. L'ABBE, G. HETEROCYCLIC ANALOGUES OF METHYLENECYCLOPROPANES. 1980, 4, 276. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173534. GABRIEL WEATHERHEAD
  173535. 11355
  173536. 12364N
  173537. 2/28/96V
  173538. KAUPP, G. PHOTOCHEMICAL REARRANGEMENTS AND FRAGMENTATIONS OF BENZENE DERIVATIVES AND ANNELATED ARENES. 80, 4, 243. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.
  173539. GABRIEL WEATHERHEAD
  173540. 11356
  173541. 12365N
  173542. 2/28/96V
  173543. SIEGEL, H.; WIMMELE, W. SYNTHESIS OF INTERMEDIATES BY RHODIUM CATALYZED HYDROFORMYLATION. 1980, 3,178. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173544. GABRIEL WEATHERHEAD
  173545. 11357
  173546. 12366N
  173547. 2/28/96V
  173548. BOTT, K. COUPLING OF SOLVOLYSIS AND C C LINKAGE: A PROMISING SYNTHETIC ROUTE TO FUNCTIONALIZED CARBOXYLIC ACIDS, ALDEHYDES, AND KETONES. 1980, 3,171. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173549. GABRIEL WEATHERHEAD
  173550. 11358
  173551. 12367N
  173552. 2/28/96V
  173553. EFFENBERGER, F. ELECTROPHILIC REAGENTS
  173554. RECENT DEVELOPMENTS AND THEIR PREPARATIVE APPLICATION. 1980, 3,151. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173555. GABRIEL WEATHERHEAD
  173556. 11359
  173557. 12368N
  173558. 2/28/96V
  173559. CLASCHKE, G. CHROMATOGRAPHIC RESOLUTION OF RACEMATES. 1980, 1, 13. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  173560. GABRIEL WEATHERHEAD
  173561. 11360
  173562. 12369N
  173563. 2/28/96
  173564. SZABO, W. A., LEE, H. T. CHIRAL STARTING MATERIALS AND REAGENTS. AN OUTLINE OF RECENT SYNTHETIC APPLICATIONS. 1980, 13, 13. ALDRICHIMICA ACTA A REVIEW.a
  173565. GABRIEL WEATHERHEAD
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  173568. 2/28/96VtWALLACE, R. G. HYDROXYLAMINE O SULFONIC ACID. A VERSATILE SYNTHETIC REAGENT. 1980,13, 3. ALDRICHIMICA ACTA A REVIEW.a
  173569. GABRIEL WEATHERHEAD
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  173573. WAN, J. K. S. THEORY AND APPLICATIONS OF CHEMICALLY INDUCED MAGNETIC POLARIZATION IN PHOTOCHEMISTRY. 1980 12, 283. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  173574. GABRIEL WEATHERHEAD
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  173577. 2/28/96VxTOMLINSON, W. J.; CHANDROSS, E. A. THE PHOTOCHEMISTRY OF RHODOPSINS. 1980, 12, 201. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  173578. GABRIEL WEATHERHEAD
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  173580. 12373N
  173581. 2/28/96VcOTTOLENGHI, M. THE PHOTOCHEMISTRY OF RHODOPSINS. 1980, 12, 97. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  173582. GABRIEL WEATHERHEAD
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  173586. LEE, E. K. C., LEWIS, R. S. PHOTOCHEMISTRY OF SIMPLE ALDEHYDES AND KETONES IN THE GAS PHASE. 1980,12,1. ADVANCES IN PHOTOCHEMISTRY A REVIEW.a
  173587. GABRIEL WEATHERHEAD
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  173591. SIEBERT, W. BORON HETEROCYCLES AS LIGANDS IN TRANSITION METAL CHEMISTRY. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173592. GABRIEL WEATHERHEAD
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  173596. FESSENDEN, R. J.; FESSENDEN, J. S. TRENDS IN ORGANOSILICON BIOLOGICAL RESEARCH. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173597. GABRIEL WEATHERHEAD
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  173600. 2/28/96VqGLADFELTER, W. L.; GEOFFROY, G. L. MIXED METAL CLUSTERS. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173601. GABRIEL WEATHERHEAD
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  173605. BRUNNER, H. CHIRAL METAL ATOMS IN OPTICALLY ACTIVE, ORGANO TRANSITION METAL COMPOUNDS. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173606. GABRIEL WEATHERHEAD
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  173608. 12379N
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  173610. VhSINN, H.; KAMINSKY, W. ZIEGLER NATTA CATALYSIS. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173611. GABRIEL WEATHERHEAD
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  173613. 12380N
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  173615. HALASA, A. F.; SCHULZ, D. N.; TATE, D. P.; MOCHEL, V. D. ORGANOLITHIUM CATALYSIS OF OLEFIN AND DIENE POLYMERIZATION. 1980, 18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173616. GABRIEL WEATHERHEAD
  173617. 11372
  173618. 12381N
  173619. 2/28/96V
  173620. BEHRENS, H. FOUR DECADES OF METAL CARBONYL CHEMISTRY IN LIQUID AMMONIA: ASPECTS AND PROSPECTS. 1980,18. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  173621. GABRIEL WEATHERHEAD
  173622. 11373
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  173624. 2/28/96VtCSICSERY, S. M. METAL CATALYZED DEHYDROCYCLIZATION OF ALKYLAROMATICS. 1979, 28, 293. ADVANCES IN CATALYSIS A REVIEW.a
  173625. GABRIEL WEATHERHEAD
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  173628. 2/28/96VnBRESLOW, R. BIOMIMETIC CONTROL OF CHEMICAL SELECTIVITY. 1980, 13, 170. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173629. GABRIEL WEATHERHEAD
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  173633. JENCKS, W. P. ENFORCED MECHANISMS OF GENERAL ACID BASE CATALYZED, CARBOCATION, CARBANION, AND LIGAND EXCHANGE REACTIONS. 1980,13,161. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173634. GABRIEL WEATHERHEAD
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  173637. 2/28/96VmGAJEWSKI, J. J. ENERGY SURFACES OF SIGMATROPIC SHIFTS. 1980, 13, 142. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173638. GABRIEL WEATHERHEAD
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  173642. BERGMAN, R. G. ISOTOPE CROSSOVER EXPERIMENTS IN CARBON CARBON BOND FORMING REACTIONS OF BINUCLEAR DIALKYLCOBALT COMPLEXES. 1980,13,113. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173643. GABRIEL WEATHERHEAD
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  173647. CASPI E. BIOSYNTHESIS OF TETRAHYMANOL BY TETRAHYMENA PYRIFORMIS: MECHANISTIC AND EVOLUTIONARY IMPLICATIONS. 1980, 13, 97. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173648. GABRIEL WEATHERHEAD
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  173652. WHITTEN, D. G. PHOTOINDUCED ELECTRON TRANSFER REACTIONS OF METAL COMPLEXES IN SOLUTION. 1980,13, 83. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173653. GABRIEL WEATHERHEAD
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  173656. 2/28/96VyBOWIE, J. H. BIMOLECULAR REACTIONS OF NUCLEOPHILES IN THE GAS PHASE. 1980,13, 76. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173657. GABRIEL WEATHERHEAD
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  173660. 2/28/96VkTHUMMEL, R. P. BENZOCYCLOBUTENE AND RELATED COMPOUNDS. 1980,13, 70. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173661. GABRIEL WEATHERHEAD
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  173664. 2/28/96VtBOEKELHEIDE, V. [2N]CYCLOPHANES: PARACYCLOPHANE TO SUPERPHANE. 1980, 13, 65. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173665. GABRIEL WEATHERHEAD
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  173668. 2/28/96VtMOSS, R. A. CARBENIC SELECTIVITY IN CYCLOPROPANATION REACTIONS. 1980,13, 58. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173669. GABRIEL WEATHERHEAD
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  173673. TIECCO, M. RADICAL IPSO ATTACK AND IPSO SUBSTITUTION IN AROMATIC COMPOUNDS. 1980,13, 51. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173674. GABRIEL WEATHERHEAD
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  173678. CALDWELL, R. A., CREED, D. EXCIPLEX INTERMEDIATES IN [2 + 2] PHOTOCYCLOADDITIONS. 1980,13, 45. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173679. GABRIEL WEATHERHEAD
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  173683. LALONDE, R. T. INTRAMOLECULAR IMINIUM ION SULFIDE CHARGE TRANSFER ASSOCIATION: A RECURRING THEME IN THE STUDY OF THIASPIRANE ALKALOIDS. 1980,13, 39. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173684. GABRIEL WEATHERHEAD
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  173688. MCLAFFERTY, F. W. TANDEM MASS SPECTROMETRY (MS/MS): A PROMISING NEW ANALYTICAL TECHNIQUE FOR SPECIFIC COMPONENT DETERMINATION IN COMPLEX MIXTURES. 1980,13, 33. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173689. GABRIEL WEATHERHEAD
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  173693. VoWENKERT, E. OXYCYCLOPROPANES IN ORGANOCHEMICAL SYNTHESIS. 1980, 13, 27. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  173694. GABRIEL WEATHERHEAD
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  173698. FENDLER, J. H. SURFACTANT VESICLES AS MEMBRANE MIMETIC AGENTS: CHARACTERIZATION AND UTILIZATION. 1980,13, 7. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
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  173703. FURUKAWA, J. STEREOREGULAR AND SEQUENCE REGULAR POLYMERIZATION OF BUTADIENE. 1980,13,1. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
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  173708. GABRIEL WEATHERHEAD
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  173711. 2/28/96VoRIDDELL, F. G. THE CONFORMATIONAL ANALYSIS OF HETEROCYCLIC COMPOUNDS. ACADEMIC PRESS: NEW YORK, 1980. A REVIEW.a
  173712. GABRIEL WEATHERHEAD
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  173716. VuPOSNER, G. H. AN INTRODUCTION TO SYNTHESIS USING ORGANOCOPPER REAGENTS. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  173717. GABRIEL WEATHERHEAD
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  173720. 2/28/96VxOTT, D. G. SYNTHESIS WITH STABLE ISOTOPES OF CARBON, NITROGEN, AND OXYGEN. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  173721. GABRIEL WEATHERHEAD
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  173725. ORCHIN, M.; KAPLAN, F.; MACOMBER, R. S.; WILSON, R. M.; ZIMMER, H. W. THE VOCABULARY OF ORGANIC CHEMISTRY. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  173726. GABRIEL WEATHERHEAD
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  173730. GABRIEL WEATHERHEAD
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  173734. LEVY, G. A.; LICHTER, R. L.; NELSON, G. L. CARBON 13 NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2ND ED. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  173735. GABRIEL WEATHERHEAD
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  173739. VpHENRY, P. M. PALLADIUM CATALYZED OXIDATION OF HYDROCARBONS. D. REDIEL PUBLISHING CO.: DORDRECHT, 1980. A REVIEW.a
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  173744. GRETHE, G., ED. ISOQUINOLINES: CHEMISTRY OF HETEROCYCLIC COMPOUNDS. VOL. 38, PART 1. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  173745. GABRIEL WEATHERHEAD
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  173749. FINLEY, K. T., ED. TRIAZOLES 1,2,3: CHEMISTRY OF HETEROCYCLIC COMPOUNDS. VOL. 39. WILEY LNTERSCIENCE: NEW YORK, 1980. A REVIEW.a
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  173754. SCHUDA, P. F. AFLATOXIN CHEMISTRY AND SYNTHESES. 1980, 91, 75. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980. A REVIEW.a
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  173759. TSUJI, J. APPLICATIONS OF PALLADIUM CATALYZED OR PROMOTED REACTIONS TO NATURAL PRODUCT SYNTHESES. 1980, 91, 29. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.
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  173764. WARREN, S. REAGENTS FOR NATURAL PRODUCT SYNTHESIS BASED ON THE PH2PO AND PHS GROUPS. 1980, 91,1. TOPICS IN CURRENT CHEMISTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
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  173769. SCANDOLA, F. PHOTOCHEMICAL REARRANGEMENTS OF COORDINATION COMPOUNDS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173770. GABRIEL WEATHERHEAD
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  173774. PADWA, A. PHOTOCHEMICAL REARRANGEMENTS OF FIVE MEMBERED RING HETEROCYCLES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173775. GABRIEL WEATHERHEAD
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  173779. NASTASI, M., STREITH J. PHOTOCHEMICAL REARRANGEMENTS INVOLVING THREE MEMBERED RINGS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173780. GABRIEL WEATHERHEAD
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  173784. WAGNER, P. J. PHOTOREARRANGEMENTS VIA BIRADICALS OF SIMPLE CARBONYL COMPOUNDS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173785. GABRIEL WEATHERHEAD
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  173789. BRYCE SMITH, D.; GILBERT, A. REARRANGEMENTS OF THE BENZENE RING. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173790. GABRIEL WEATHERHEAD
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  173794. SCHAFFNER, K.; DEMUTH, M. PHOTOCHEMICAL REARRANGEMENTS OF CONJUGATED CYCLIC DIENONES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173795. GABRIEL WEATHERHEAD
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  173799. SCHUSTER, D. I. PHOTOCHEMICAL REARRANGEMENTS OF ENONES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173800. GABRIEL WEATHERHEAD
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  173804. ZIMMERMAN, H. E. THE DI PI METHANE (ZIMMERMAN) REARRANGEMENT. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173805. GABRIEL WEATHERHEAD
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  173809. DAUBEN, W. G.; MCINNIS, E. L.; MICHNO, D. M. PHOTOCHEMICAL REARRANGEMENTS IN TRIENES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173810. GABRIEL WEATHERHEAD
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  173814. SALTIEL, J., CHARLTON, J. L. CIS TRANS ISOMERIZATION OF OLEFINS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173815. GABRIEL WEATHERHEAD
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  173819. TURRO, N. J.; RAMAMURTHY, V. CHEMICAL GENERATION OF EXCITED STATES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 3 A REVIEW.a
  173820. GABRIEL WEATHERHEAD
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  173824. COTTON, F. A.; HANSON, B. E. FLUXIONAL MOLECULES: REVERSIBLE THERMAL INTRAMOLECULAR REARRANGEMENTS OF METAL CARBONYLS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173825. GABRIEL WEATHERHEAD
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  173829. JACKSON, A. G.; SARGESON, A. M. REARRANGEMENT IN COORDINATION COMPLEXES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173830. GABRIEL WEATHERHEAD
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  173834. WESTHEIMER, F. H. THE POLYTOPAL REARRANGEMENT AT PHOSPHORUS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173835. GABRIEL WEATHERHEAD
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  173837. 12427N
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  173839. BROOK, A. G.; BASSINDALE, A. R. MOLECULAR REARRANGEMENTS OF ORGANOSILICON COMPOUNDS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173840. GABRIEL WEATHERHEAD
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  173842. 12428N
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  173844. PELTER, A. REARRANGEMENTS INVOLVING BORON. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173845. GABRIEL WEATHERHEAD
  173846. 11420
  173847. 12429N
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  173849. EPIOTIS, N.; SHAIK, S.; ZANDER, W. REARRANGEMENTS: A THEORETICAL APPROACH. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 2 A REVIEW.a
  173850. GABRIEL WEATHERHEAD
  173851. 11421
  173852. 12430N
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  173854. HUNTER, D. H.; STOTHERS, J. B.; WARNHOFF, E. W. REARRANGEMENTS IN CARBANIONS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173855. GABRIEL WEATHERHEAD
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  173859. BERSON, J. A. HYPOTHETICAL BIRADICAL PATHWAYS IN THERMAL UNIMOLECULAR REARRANGEMENTS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173860. GABRIEL WEATHERHEAD
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  173862. 12432N
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  173864. BECKWITH, A. L. J.; INGOLD, K. U. FREE RADICAL REARRANGEMENTS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173865. GABRIEL WEATHERHEAD
  173866. 11424
  173867. 12433N
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  173869. JONES, W. M. REARRANGEMENTS OF CARBENES AND NITRENES. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173870. GABRIEL WEATHERHEAD
  173871. 11425
  173872. 12434N
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  173874. BOWEN, R. D.; WILLIAMS, D. H. GAS PHASE ION REARRANGEMENTS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173875. GABRIEL WEATHERHEAD
  173876. 11426
  173877. 12435N
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  173879. SAUNDERS, M.; CHANDRASEKHAR, J.; SCHLEYER, P. V. R. REARRANGEMENTS OF CARBOCATIONS. REARRANGEMENTS IN GROUND AND EXCITED STATES, P. DEMAYO, ED., ACADEMIC PRESS: NEW YORK, 1980. VOLUME 1 A REVIEW.a
  173880. GABRIEL WEATHERHEAD
  173881. 11427
  173882. 12436N
  173883. 2/28/96VnSCHMIDT, A. H. THE CHEMISTRY OF SQUARAINES. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173884. GABRIEL WEATHERHEAD
  173885. 11428
  173886. 12437N
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  173888. BELLUS, D. SYNTHESES OF HIGHLY OXIDIZED CYCLOBUTANES VIA [2 + 2] CYCLOADDITION REACTIONS OF KETENES. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173889. GABRIEL WEATHERHEAD
  173890. 11429
  173891. 12438N
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  173893. FEDER J. THE STRUCTURAL PHASE TRANSITION AND DIELECTRIC PROPERTIES OF SQUARIC ACID. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173894. GABRIEL WEATHERHEAD
  173895. 11430
  173896. 12439N
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  173898. ITO, M.; KAYA, K.; TAKAHASHI, M. RAMAN SPECTRA AND JAHN TELLER EFFECTS OF OXOCARBON DIANIONS. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173899. GABRIEL WEATHERHEAD
  173900. 11431
  173901. 12440N
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  173903. SCHARF, H. D.; FRAUENRACH, H. THE MYCOTOXIN MONILIFORMIN AND RELATED SUBSTANCES. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173904. GABRIEL WEATHERHEAD
  173905. 11432
  173906. 12441N
  173907. 2/28/96V|MICHL, J.; WEST, R. EXCITED STATES OF OXOCARBON DIANIONS. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173908. GABRIEL WEATHERHEAD
  173909. 11433
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  173912. FATIADI, A. J. NEW BOND DELOCALIZED (DICYANOMETHYLIDENE) CROCONATE DERIVATIVES: CROCONATE VIOLET AND CROCONATE BLUE . OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173913. GABRIEL WEATHERHEAD
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  173915. 12443N
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  173917. SCHWARTZ, L. M.; GELB, R. I.; LAUFER, D. A. PHYSICAL CHEMISTRY OF AQUEOUS OXOCARBONS. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173918. GABRIEL WEATHERHEAD
  173919. 11435
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  173921. 2/28/96V|SEITZ, G. H. THIOXOCARBON DIANIONS AND THEIR DERIVATIVES. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173922. GABRIEL WEATHERHEAD
  173923. 11436
  173924. 12445N
  173925. 2/28/96VbWEST, R. HISTORY OF OXOCARBONS. OXOCARBONS, R. WEST, ED., ACADEMIC PRESS: NEW YORK, 1980 A REVIEW.a
  173926. GABRIEL WEATHERHEAD
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  173929. 2/28/96V^SAINSBURY M. MODERN METHODS OF ARYL ARYL BOND FORMATION. 1980, 36, 3327. TETRAHEDRON A REVIEW.a
  173930. GABRIEL WEATHERHEAD
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  173933. 2/28/96VzHORWELL, D. C. SYNTHETIC STRATEGIES TO THE ERGOLINE RING SYSTEMS OF ERGOT ALKALOIDS. 1980, 36, 3123. TETRAHEDRON A REVIEW.a
  173934. GABRIEL WEATHERHEAD
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  173938. TOROMANOFF, E. DYNAMIC STEREOCHEMISTRY OF THE 5 , 6AND 7 MEMBERED RINGS USING THE TORSION ANGLE NOTATION. 1980, 36, 2809. TETRAHEDRON A REVIEW.a
  173939. GABRIEL WEATHERHEAD
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  173943. GREEN, M. M. A STEREOCHEMICAL BRIDGE BETWEEN MASS SPECTROMETRY AND FREE RADICAL CHEMISTRY. 1980, 36, 2687. TETRAHEDRON A REVIEW.a
  173944. GABRIEL WEATHERHEAD
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  173947. 2/28/96VlKRIEF, A. SYNTHETIC METHODS USING A HETEROSUBSTITUTED ORGANOMETALLICS. 1980, 36, 2531. TETRAHEDRON A REVIEW.a
  173948. GABRIEL WEATHERHEAD
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  173952. HASLAM, E. RECENT DEVELOPMENTS IN METHODS FOR THE ESTERIFICATION AND PROTECTION OF THE CARBOXYL GROUP. 1980, 36, 2409. TETRAHEDRON A REVIEW.a
  173953. GABRIEL WEATHERHEAD
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  173956. 2/28/96VVCALUWE, P. HETEROANNELATION OF O AMINOALDEHYDES. 1980, 36, 2359. TETRAHEDRON A REVIEW.a
  173957. GABRIEL WEATHERHEAD
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  173961. )VYCHAN, T. H.; ONG, B. S. CHEMISTRY OF ALLENE OXIDES. 1980, 36, 2269. TETRAHEDRON A REVIEW.a
  173962. GABRIEL WEATHERHEAD
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  173966. NEWTON, R. F., ROBERTS, S. M. STERIC CONTROL IN PROSTAGLANDIN SYNTHESIS INVOLVING BICYCLIC AND TRICYCLIC INTERMEDIATES. 1980, 36, 2163. TETRAHEDRON A REVIEW.a
  173967. GABRIEL WEATHERHEAD
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  173971. HALL, C. R.; INCH, T. D. PHOSPHORUS STEREOCHEMISTRY. MECHANISTIC IMPLICATIONS OF THE OBSERVED STEREOCHEMISTRY OF BOND FORMING AND BREAKING PROCESSES AT PHOSPHORUS IN SOME 5  AND 6 MEMBERED CYCLIC PHOSPHORUS ESTERS. 1980, 36, 2059. TETRAHEDRON A REVIEW.a
  173972. GABRIEL WEATHERHEAD
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  173975. 2/28/96VsBARRETT G. C. THE CHEMISTRY OF 1,3 THIAZOLINONE HYDROXY I,3 THIAZOLE SYSTEMS. 1980, 36, 2023. TETRAHEDRON A REVIEW.a
  173976. GABRIEL WEATHERHEAD
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  173980. MAGID, R. M. NUCLEOPHILIC AND ORGANOMETALLIC DISPLACEMENT REACTIONS OF ALLYLIC COMPOUNDS: STEREO  AND REGIOCHEMISTRY. 1980, 36,1901. TETRAHEDRON A REVIEW.a
  173981. GABRIEL WEATHERHEAD
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  173984. 2/28/96VcBECKER, K. B. CYCLOALKENES BY INTRAMOLECULAR WITTIG REACTION. 1980, 36, 1717. TETRAHEDRON A REVIEW.a
  173985. GABRIEL WEATHERHEAD
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  173989. SHEA, K. RECENT DEVELOPMENTS IN THE SYNTHESIS, STRUCTURE AND CHEMISTRY OF BRIDGEHEAD ALKENES. 1980, 36,1683. TETRAHEDRON A REVIEW.a
  173990. GABRIEL WEATHERHEAD
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  173993. 2/28/96VZSULTANBAWA, M. U. S. XANTHONOIDS OF TROPICAL PLANTS. 1980, 36, 1465. TETRAHEDRON A REVIEW.a
  173994. GABRIEL WEATHERHEAD
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  173997. 2/28/96VhSCHMIDT A. H. REACTIONS OF SQUARIC ACID AND ITS DERIVATIVES (IN GER.). 1980,12, 961. SYNTHESIS A REVIEW.a
  173998. GABRIEL WEATHERHEAD
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  174002. GROUTAS, W. C.; FELKER, D. SYNTHETIC APPLICATIONS OF CYANOTRIMETHYLSILANE, IODOTRIMETHYLSILANE, AZIDOTRIMETHYLSILANE, AND METHYLTHIOMETHYLTRIMETHYLSILANE. 1980, 11, 861. SYNTHESIS A REVIEW.a
  174003. GABRIEL WEATHERHEAD
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  174007. WAGNER JAUREGG, T. THERMAL AND PHOTOCHEMICAL ADDITIONS OF DIENOPHILES TO ARENES AND HETEROCYCLES (IN GER.). 1980, 10, 769. SYNTHESIS A REVIEW.a
  174008. GABRIEL WEATHERHEAD
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  174011. 2/28/96VUWALSH, D. A. THE SYNTHESIS OF 2 AMINOBENZOPHENONES. 1980, 9, 677. SYNTHESIS A REVIEW.a
  174012. GABRIEL WEATHERHEAD
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  174015. 2/28/96VvBECHER, J. SYNTHESIS AND REACTIONS OF GLUTACONALDEHYDE AND 5 AMINO 2,4 PENTADIENALS. 1980, 8, 589. SYNTHESIS A REVIEW.a
  174016. GABRIEL WEATHERHEAD
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  174019. 2/28/96VTCOPPOLA, G. M. THE CHEMISTRY OF ISATOIC ANHYDRIDE. 1980, 7, 505. SYNTHESIS A REVIEW.a
  174020. GABRIEL WEATHERHEAD
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  174022. 12467N
  174023. 2/28/96
  174024. YAKHIMOVICH, R. I. THE SYNTHESIS OF ACTIVE METABOLITES AND ANALOGUES OF VITAMIN D3. 1980, 49, 371. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174025. GABRIEL WEATHERHEAD
  174026. 11459
  174027. 12468N
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  174029. KRUGLAYA, O. A.; VYAZANKIN, N. S. ORGANOMETALLIC DERIVATIVES OF DIAZOALKANES. 1980, 49, 357. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174030. GABRIEL WEATHERHEAD
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  174034. ZEFIROV, N. S., MAKHON'KOV, D. I. ADVANCES IN THE CHEMISTRY OF PERNITRILES (CYANOCARBONS). 1980, 49, 337. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174035. GABRIEL WEATHERHEAD
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  174038. 2/28/96V{SHKLOVER, V. E.; STRUCHKOV, YU. T. THE STRUCTURE OF ORGANOCYCLOSILOXANES. 1980, 49, 272. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174039. GABRIEL WEATHERHEAD
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  174042. 2/28/96VpBUKHTIAROV, A. V.; TOMILOV, A. P. CATHODIC COUPLING REACTIONS. 1980, 49, 249. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174043. GABRIEL WEATHERHEAD
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  174047. YANDOVSKII, V. N.; GIDASPOV, V. B.; TSELINSKII, 1. V. THE FORMATION OF THE AZOXY GROUP IN REACTIONS INVOLVING ANIONS WITH NITROGEN NITROGEN BONDS. 1980, 49, 237. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174048. GABRIEL WEATHERHEAD
  174049. 11464
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  174051. 2/28/96VUGAKHOKIDZ, R. A. SACCHARINIC ACIDS. 1980, 49, 222. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174052. GABRIEL WEATHERHEAD
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  174056. MEL'NIKOV M. YA.; FOK, N. V. PHOTOCHEMICAL REACTIONS OF FREE RALICALS IN THE SOLID PHASE. 1980, 49, 131 RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174057. GABRIEL WEATHERHEAD
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  174061. YUDEVICH, V. I.; SOKOLOV, L. B.; IONIN, B. I. PHOSPHINATES ( HYPOPHOSPHITES ) AND THEIR REACTIVITY. 1980, 49, 46. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174062. GABRIEL WEATHERHEAD
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  174065. 2/28/96VtYSAHUNSKII, V. G.; KHOLODOV, L. E. THE CHEMISTRY OF SYDNONE IMINES. 1980, 49, 28. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174066. GABRIEL WEATHERHEAD
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  174070. KLYUEV, M. V.; KHIDEKEL', M. L. CATALYTIC AMINATION OF ALCOHOLS, ALDEHYDES, AND KETONES. 1980, 49,14. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174071. GABRIEL WEATHERHEAD
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  174075. SOLODOVNIKOV, S. P.; BUBNOV, N. N.; PROKOF'EF, A. I. STEREOCHEMISTRY OF THE REACTIONS OF PHOSPHORUS CONTAINING FREE RADICALS. 1980, 49,1. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174076. GABRIEL WEATHERHEAD
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  174080. NUDELMAN, A. THE CHEMISTRY OF OPTICALLY ACTIVE SULFUR COMPOUNDS. PART IV. 1980, 9,1. PHOSPHORUS AND SULFUR AND THE RELATED ELEMENTS A REVIEW.a
  174081. GABRIEL WEATHERHEAD
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  174084. 2/28/96VZWEST, R. CHEMISTRY OF THE OXOCARBONS. 1980, 20, 300. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174085. GABRIEL WEATHERHEAD
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  174088. 2/28/96VaMITCHELL, R. H. UNDERSTANDING BENZANNULENES. 1980, 20, 294. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174089. GABRIEL WEATHERHEAD
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  174093. ILIC, P.; SINKOVIC, B.; TRINAJSTIC, N. TOPOLOGICAL RESONANCE ENERGIES OF CONJUGATED STRUCTURES. 1980, 20, 258. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174094. GABRIEL WEATHERHEAD
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  174097. 2/28/96VjPAQUETTE, L. A. THE EVOLUTION OF HEPTALENE CHEMISTRY. 1980, 20, 233. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174098. GABRIEL WEATHERHEAD
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  174101. 2/28/96VQVOGEL, E. BRIDGED ANNULENES. 1980, 20, 215. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174102. GABRIEL WEATHERHEAD
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  174105. 2/28/96VoDALE, J. THE CONFORMATION OF FREE AND COMPLEXES OLIGOETHERS. 1980, 20, 3. ISRAEL JOURNAL OF CHEMISTRY A REVIEW.a
  174106. GABRIEL WEATHERHEAD
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  174110. HUGHES, A. N. SYNTHETIC APPLICATIONS OF DIMETHYL ACETYLENEDICARBOXYLATE IN PHOSPHORUS HETEROCYCLIC CHEMISTRY. 1981, 15, 637. HETEROCYCLES A REVIEW.a
  174111. GABRIEL WEATHERHEAD
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  174115. KVgINUBUSHI Y., HARAYAMA, T. TOTAL SYNTHESIS OF LYCOPODIUM ALKALOIDS. 1981,15, 611. HETEROCYCLES A REVIEW.a
  174116. GABRIEL WEATHERHEAD
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  174120. SAKAMOTO, T.; YAMANAKA, H. CONVERSION OF SIMPLE PYRIMIDINES INTO DERIVATIVES WITH A CARBON FUNCTIONAL GROUP. 1981, 15, 583. HETEROCYCLES A REVIEW.a
  174121. GABRIEL WEATHERHEAD
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  174125. NISHIWAKI, T.; ABE, N. RECENT PROGRESS IN THE CHEMISTRY OF AZAAZULENES: SYNTHETIC METHODOLOGY AND CHEMICAL REACTIONS. 1981,15, 547. HETEROCYCLES A REVIEW.a
  174126. GABRIEL WEATHERHEAD
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  174129. 2/28/96VlREBEK, JR., J. PROGRESS IN THE DEVELOPMENT OF NEW EPOXIDATION REAGENTS. 1981,15, 517. HETEROCYCLES A REVIEW.a
  174130. GABRIEL WEATHERHEAD
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  174132. 12491N
  174133. 2/28/96V
  174134. BOBBITT, J. M.; KULKARNI, C. L.; WILLIS, J. P. THE ELECTROOXIDATION OF PYRROLE, INDOLE, CARBAZOLE, AND THEIR DERIVATIVES. 1981,15, 495. HETEROCYCLES A REVIEW.a
  174135. GABRIEL WEATHERHEAD
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  174137. 12492N
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  174139. PVzSEMPLE, J. E.; JOULLIE, M. M. SYNTHESIS OF REDUCED FURANS AND 3(2H) DIHYDROFURANONES. 1980,14,1825. HETEROCYCLES A REVIEW.a
  174140. GABRIEL WEATHERHEAD
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  174143. 2/28/96VVSLIWA, W. CYCLOADDITION REACTIONS OF PYRIDINES. 1980, 14, 1793. HETEROCYCLES A REVIEW.a
  174144. GABRIEL WEATHERHEAD
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  174147. 2/28/96V{KATO, T.; KATAGIRI, N., YAMAMOTO, Y. RECENT ADVANCES IN THE CHEMISTRY OF 1,3 0XAZINES. 1980, 9,1333. HETEROCYCLES A REVIEW.a
  174148. GABRIEL WEATHERHEAD
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  174150. 12495N
  174151. 2/28/96VfSKONIECZNY S. REACTIONS AT C 9 OF ACRIDINE DERIVATIVES. PART XXV. 1980, 7, 985. HETEROCYCLES A REVIEW.a
  174152. GABRIEL WEATHERHEAD
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  174155. 2/28/96VhWARREN, S. PHOSPHORUS AND SULPHUR REAGENTS IN SYNTHESIS. 1980, 20, 824. CHEMISTRY AND INDUSTRY A REVIEW.a
  174156. GABRIEL WEATHERHEAD
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  174158. 12497N
  174159. 2/28/96
  174160. BAKER, R. CARBON CARBON BOND FORMING REACTIONS OF ALLYL COMPLEXES OF NICKEL, PALLADIUM AND IRON. 1980, 20, 816. CHEMISTRY AND INDUSTRY A REVIEW.a
  174161. GABRIEL WEATHERHEAD
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  174164. 2/28/96VVPATTENDEN, G. THE PHOTON IN SYNTHESIS. 1980, 20, 812. CHEMISTRY AND INDUSTRY A REVIEW.a
  174165. GABRIEL WEATHERHEAD
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  174167. 12499N
  174168. 2/28/96V
  174169. SUTHERLAND, J. K. THE INITIATION OF CYCLIZATION USING 3 METHYLCYCLOHEX 2 ENONE DERIVATIVES. 1980, 3, 265. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  174170. GABRIEL WEATHERHEAD
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  174172. 12500N
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  174174. BOYER, J. H. INCREASING THE INDEX OF COVALENT OXYGEN BONDING AT NITROGEN ATTACHED TO CARBON. 1980, 6, 495. CHEMICAL REVIEWS A REVIEW.a
  174175. GABRIEL WEATHERHEAD
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  174177. 12501N
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  174179. BARTSCH, R. A.; ZAVADA, J. STEREOCHEMICAL AND BASE SPECIES DICHOTOMIES IN OLEFIN FORMING E2 ELIMINATIONS. 1980, 6, 453. CHEMICAL REVIEWS A REVIEW.a
  174180. GABRIEL WEATHERHEAD
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  174182. 12502N
  174183. 2/28/96
  174184. ZVbCLARK, J. H. FLUORIDE ION AS A BASE IN ORGANIC SYNTHESIS. 1980, 5, 429. CHEMICAL REVIEWS A REVIEW.a
  174185. GABRIEL WEATHERHEAD
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  174187. 12503N
  174188. 2/28/96VgFREEMAN, F. PROPERTIES AND REACTIONS OF YLIDENEMALONONITRILES. 1980, 4, 329. CHEMICAL REVIEWS A REVIEW.a
  174189. GABRIEL WEATHERHEAD
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  174192. 2/28/96VsSINGH, S. P., STERNBERG, V. I., PARMAR, S. S. PHOTOCHEMISTRY OF ALKALOIDS. 1980, 3, 269. CHEMICAL REVIEWS A REVIEW.a
  174193. GABRIEL WEATHERHEAD
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  174195. 12505N
  174196. 2/28/96V
  174197. COLLET, A.; BRIENNE, M. J.; JACQUES, J. OPTICAL RESOLUTION BY DIRECT CRYSTALLIZATION OF ENANTIOMER MIXTURES. 1980 3, 215. CHEMICAL REVIEWS A REVIEW.a
  174198. GABRIEL WEATHERHEAD
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  174202. GEORGE, M. V.; MITRA, A., SUKUMARAN, K. B. THERMAL AND PHOTOCHEMICAL TRANSFORMATIONS OF HETERO 1,3,5 HEXATRIENES INTO FIVE MEMBERED RINGS
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  174204. GABRIEL WEATHERHEAD
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  174208. HUISGEN, R. 1,5 ELECTROCYCLIZATIONS
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  174210. GABRIEL WEATHERHEAD
  174211. 11499
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  174214. PINO, P.; MULHAUPT, R. STEREOSPECIFIC POLYMERIZATION OF PROPYLENE: AN OVERLOOK. 1980,19, 857. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174215. GABRIEL WEATHERHEAD
  174216. 11500
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  174219. LE NOBLE, W. J.; KELM, H. CHEMISTRY IN COMPRESSED SOLUTIONS. 1980,19, 841. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174220. GABRIEL WEATHERHEAD
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  174224. SAUER, J.; SUSTMANN, R. MECHANISTIC ASPECTS OF DIELS ALDER REACTIONS: A CRITICAL SURVEY. 1980,19, 779. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174225. GABRIEL WEATHERHEAD
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  174229. ADAM, W., DE LUCCHI O. THE SYNTHESIS OF UNUSUAL ORGANIC MOLECULES FROM AZOALKANES [NEW SYNTHETIC METHODS (33)]. 1980,19, 762. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174230. GABRIEL WEATHERHEAD
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  174234. TURRO, N. J.; GRATZEL, M.; BRAUN, A. M. PHOTOPHYSICAL AND PHOTOCHEMICAL PROCESSES IN MICELLAR SYSTEMS. 1980, 19, 675. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174235. GABRIEL WEATHERHEAD
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  174239. JOCHUM, C., GASTEIGERN, J., UGI, I. THE PRINCIPLE OF MINIMUM CHEMICAL DISTANCE. 1980,19, 495. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  174240. GABRIEL WEATHERHEAD
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  174243. 2/28/96VuMAGNUS, P. ORGANOSILICON REACTIONS FOR CARBON CARBON BOND FORMING REACTIONS. 1980,13, 43. ALDRICHIMICA ACTA A REVIEW.a
  174244. GABRIEL WEATHERHEAD
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  174247. 2/28/96V[FRIEDRICHSEN, W. BENZO[C]FURANS. 1980, 26,135. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.
  174248. GABRIEL WEATHERHEAD
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  174251. 2/28/96VfMETH COHN, O.; TARNOWSKI, B. THIOCOUMARINS. 1980, 26 115. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  174252. GABRIEL WEATHERHEAD
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  174254. 12517N
  174255. 2/28/96V
  174256. RAMSDEN, C. A. HETEROCYCLIC BETAIN DERIVATIVES OF ALTERNANT HYDROCARBONS. 1980, 26, 3. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  174257. GABRIEL WEATHERHEAD
  174258. 11509
  174259. 12518N
  174260. 2/28/96V
  174261. DEY, P. M. BIOCHEMISTRY OF A D GALACTOSIDIC LINKAGES IN THE PLANT KINGDOM. 1980, 37, 284. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  174262. GABRIEL WEATHERHEAD
  174263. 11510
  174264. 12519N
  174265. 2/28/96V
  174266. STOWELL, C. P.; LEE, Y. C. NEOGLYCOPROTEINS: THE PREPARATION AND APPLICATION OF SYNTHETIC CYCLOPROTEINS. 1980, 37, 225. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  174267. GABRIEL WEATHERHEAD
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  174269. 12520N
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  174271. CRAWFORD, T. C.; CRAWFORD, S. A. SYNTHESIS OF L ASCORBIC ACID. 1980, 37, 79. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  174272. GABRIEL WEATHERHEAD
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  174274. 12521N
  174275. 2/28/96V
  174276. VON SONNTAG, C. FREE RADICAL REACTIONS OF CARBOHYDRATES BY RADIATION TECHNIQUES. 1980, 37, 7. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  174277. GABRIEL WEATHERHEAD
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  174279. 12522N
  174280. 2/28/96VnPAAL, Z. METAL CATALYZED CYCLIZATION REACTIONS OF HYDROCARBONS. 1980, 29, 273. ADVANCES IN CATALYSIS A REVIEW.a
  174281. GABRIEL WEATHERHEAD
  174282. 11514
  174283. 12523N
  174284. 2/28/96V|YAMAZAKI, Y.; KAWAI, T. HYDROGENOLYTIC BEHAVIOR OF ASYMMETRIC DIARYLMETHANES. 1980, 29, 229. ADVANCES IN CATALYSIS A REVIEW.a
  174285. GABRIEL WEATHERHEAD
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  174288. 2/28/96VgROYER, G. P. ENZYME LIKE SYNTHETIC CATALYSTS (SYNZYMES). 1980, 29, 197. ADVANCES IN CATALYSIS A REVIEW.a
  174289. GABRIEL WEATHERHEAD
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  174291. 12525N
  174292. 2/28/96
  174293. KRAUS, M. ORGANIC SUBSTITUENT EFFECTS AS PROBES FOR THE MECHANISM OF SURFACE CATALYSIS. 1980, 29,151 ADVANCES IN CATALYSIS A REVIEW.a
  174294. GABRIEL WEATHERHEAD
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  174296. 12526N
  174297. 2/28/96V
  174298. MAATMAN, R. W. SITE DENSITY AND ENTROPY CRITERIA IN IDENTIFYING RATE DETERMINING STEPS IN SOLID CATALYZED REACTIONS. 1980, 29, 97. ADVANCES IN CATALYSIS A REVIEW.a
  174299. GABRIEL WEATHERHEAD
  174300. 11518
  174301. 12527N
  174302. 2/28/96VnROBERTS, M. W. PHOTOELECTRON SPECTROSCOPY AND SURFACE CHEMISTRY. 1980, 29, 55. ADVANCES IN CATALYSIS A REVIEW.a
  174303. GABRIEL WEATHERHEAD
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  174305. 12528N
  174306. 2/28/96VzMADIX, R. J. REACTION KINETICS AND MECHANISM ON METAL SINGLE CRYSTAL SURFACES. 1980, 29,1. ADVANCES IN CATALYSIS A REVIEW.a
  174307. GABRIEL WEATHERHEAD
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  174309. 12529N
  174310. 2/28/96V
  174311. PEARSON, A. J. TRICARBONYL(DIENE)IRON COMPLEXES: SYNTHETICALLY USEFUL PROPERTIES. 1980,13, 463. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174312. GABRIEL WEATHERHEAD
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  174316. HEGARTY, A. F. STEREOSPECIFIC REACTIONS OF NITRILIUM LONS AND ANALOGOUS 1,3 DIPOLES. 1980,13, 448. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174317. GABRIEL WEATHERHEAD
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  174320. 2/28/96VgSNIDER, B. B. LEWIS ACID CATALYZED ENE REACTIONS. 1980 13, 426. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174321. GABRIEL WEATHERHEAD
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  174325. TURRO, N. J.; BRAEUTLER, B. MAGNETIC FIELD AND MAGNETIC ISOTOPE EFFECTS IN ORGANIC PHOTOCHEMICAL REACTIONS. 1980 13, 369. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174326. GABRIEL WEATHERHEAD
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  174329. 2/28/96VmOLAH, G. A. SOME NEW SYNTHETIC REAGENTS AND REACTIONS. 1980, 13, 330. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174330. GABRIEL WEATHERHEAD
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  174333. 2/28/96V}MCCULLOUGH, J. J. O XYLYLENES AND ISOINDENES AS REACTION INTERMEDIATES. 1980,13, 270. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174334. GABRIEL WEATHERHEAD
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  174338. HURLEY, L. H. BIOSYNTHETIC PATHWAYS LEADING TO THE PYRROLO[1,4]BENZODIAZEPINE ANTIBIOTICS. 1980,13, 263. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174339. GABRIEL WEATHERHEAD
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  174343. OVERMAN, L. E. ALLYLIC AND PROPARGYLIC IMIDIC ESTERS IN ORGANIC SYNTHESIS. 1980,13, 218. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174344. GABRIEL WEATHERHEAD
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  174348. MARSHALL, J. A. TRANS CYCLOALKENES AND [A.B]BETWEENANENES, MOLECULAR JUMP ROPES AND DOUBLE BOND SANDWICHES. 1980, 13, 213. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174349. GABRIEL WEATHERHEAD
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  174352. 2/28/96VpBEGUE, J. P. CHARPENTIER MORIZE, M. A ACYLCARBENIUM IONS. 1980, 13, 207. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174353. GABRIEL WEATHERHEAD
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  174357. MUSKER, W. K. CHEMISTRY OF ALIPHATIC THIOETHER CATION RADICALS AND DICATIONS. 1980,13, 200. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174358. GABRIEL WEATHERHEAD
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  174362. GRILLER, D.; INGOLD, K. U. ELECTRON PARAMAGNETIC RESONANCE IN PHYSICAL ORGANIC CHEMISTRY. 1980 13,193. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  174363. GABRIEL WEATHERHEAD
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  174366. 2/28/96V{STIRLING, C. J. M., ED. THE CHEMISTRY OF THE SULPHONIUM GROUP: PARTS 1 AND 2. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174367. GABRIEL WEATHERHEAD
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  174370. 2/28/96V[STEYN, P. S., ED. THE BIOSYNTHESIS OF MYCOTOXINS. ACADEMIC PRESS: NEW YORK, 1980. A REVIEW.a
  174371. GABRIEL WEATHERHEAD
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  174375. SCHLUNEGGER, U. P. ADVANCED MASS SPECTROMETRY: APPLICATIONS IN ANALYTICAL AND ORGANIC CHEMISTRY. PERGAMON PRESS: NEW YORK, 1980. A REVIEW.a
  174376. GABRIEL WEATHERHEAD
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  174380. QUIN, L. D. THE HETEROCYCLIC CHEMISTRY OF PHOSPHORUS: SYSTEMS BASED ON THE PHOSPHORUS CARBON BOND. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174381. GABRIEL WEATHERHEAD
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  174383. 12545N
  174384. 2/28/96
  174385. PRESTON, P. N., STEVENS, M. F. G., TENNANT, G. BENZIMIDAZOLES AND CONGENERIC TRICYCLIC COMPOUNDS. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  174386. GABRIEL WEATHERHEAD
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  174388. 12546N
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  174390. PIGMAN, W.; HORTON, D.; WANDER, J. D., EDS. THE CARBOHYDRATES: CHEMISTRY AND BIOCHEMISTRY, SECOND EDITION, VOL. 1B. ACADEMIC PRESS: NEW YORK, 1980. A REVIEW.a
  174391. GABRIEL WEATHERHEAD
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  174394. 2/28/96VsNAUMANN, K. CHEMISTRY OF SYNTHETIC PYRETHRIUM INSECTICIDES (IN GERMAN). SPRINGER VERLAG: HEIDLBERG, 1981. A REVIEW.a
  174395. GABRIEL WEATHERHEAD
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  174397. 12548N
  174398. 2/28/96VaKYRIACOU, D. K. BASICS OF ELECTROORGANIC SYNTHESIS. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174399. GABRIEL WEATHERHEAD
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  174402. 2/28/96VgKENNEDY J. P.; MARECHAL, E. CARBOCATIONIC POLYMERIZATION. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174403. GABRIEL WEATHERHEAD
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  174405. 12550N
  174406. 2/28/96
  174407. VxIZATT, R. M.; CHRISTENSEN, J. J. PROGRESS IN MACROCYCLIC CHEMISTRY, VOL. 2. WILEY INTERSCIENCE: NEW YORK 1981. A REVIEW.a
  174408. GABRIEL WEATHERHEAD
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  174410. 12551N
  174411. 2/28/96V
  174412. HODGE, P.; SHERINGTON, D. C., EDS. POLYMER SUPPORTED REACTIONS IN ORGANIC SYNTHESIS. WILEY INTERSCIENCE: NEW YORK, 1980. A REVIEW.a
  174413. GABRIEL WEATHERHEAD
  174414. 11543
  174415. 12552N
  174416. 2/28/96VoHESS, M.; TRANSLATED FROM GERMAN, R. C. BICK. ALKALOID CHEMISTRY. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174417. GABRIEL WEATHERHEAD
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  174420. 2/28/96VcGREENE, T. W. PROTECTIVE GROUPS IN ORGANIC SYNTHESIS. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174421. GABRIEL WEATHERHEAD
  174422. 11545
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  174424. 2/28/96V`GOLDSTEIN, I. S., ED. ORGANIC CHEMICALS FROM BIOMASS. CRS PRESS: BOCA RATON, FL, 1981. A REVIEW.a
  174425. GABRIEL WEATHERHEAD
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  174429. EMANUEL, N. M.; ZAIKOV, G. E.; MAIZUS, Z. K. OXIDATION OF ORGANIC COMPOUNDS: SOLVENT EFFECTS IN RADICAL REACTIONS. PERGAMON PRESS: NEW YORK, 1981. A REVIEW.a
  174430. GABRIEL WEATHERHEAD
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  174433. 2/28/96VYDOBLER, M. IONOPHORES AND THEIR STRUCTURES. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174434. GABRIEL WEATHERHEAD
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  174437. 2/28/96VkDHAR, D. N. THE CHEMISTRY OF CHALCONES AND RELATED COMPOUNDS. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174438. GABRIEL WEATHERHEAD
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  174441. 2/28/96VnCORDELL, G. A. INTRODUCTION TO ALKALOIDS: A BIOGENETIC APPROACH. WILEY INTERSCIENCE: NEW YORK, 1981. A REVIEW.a
  174442. GABRIEL WEATHERHEAD
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  174445. 2/28/96VbCORCORAN, J. W., ED. BIOSYNTHESIS: ANTIBIOTICS, VOL. 4. SPRINGER VERLAG: NEW YORK, 1981. A REVIEW.a
  174446. GABRIEL WEATHERHEAD
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  174449. 2/28/96VZARCAMONE, F. DOXORUBICIN: ANTICANCER ANTIBIOTICS ACADEMIC PRESS: NEW YORK, 1981. A REVIEW.a
  174450. GABRIEL WEATHERHEAD
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  174454. THOMAS, A. F.; BESSIERE, Y. THE SYNTHESIS OF MONOTERPENES, 1971 1979, P 451. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. 4, J. APSIMON, ED., WILEY INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174455. GABRIEL WEATHERHEAD
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  174459. BINDRA, J. S. THE SYNTHESIS OF PROSTAGLANDINS, P 353. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. 4, J. APSIMON, ED., WILEY INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174460. GABRIEL WEATHERHEAD
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  174464. WIERENGA, W. THE TOTAL SYNTHESIS OF IONOPHORES, P 263. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. 4, J. APSIMON, ED., WILEY INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174465. GABRIEL WEATHERHEAD
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  174469. RAZDAN, R. K. THE TOTAL SYNTHESIS OF CANNABINOIDS, P 185. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. 4, J. APSIMON, ED., WILEY INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174470. GABRIEL WEATHERHEAD
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  174474. MORI, K. THE SYNTHESIS OF INSECT PHEROMONES, P 1. THE TOTAL SYNTHESIS OF NATURAL PRODUCTS, VOL. 4, J. APSIMON, ED., WILEY INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174475. GABRIEL WEATHERHEAD
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  174479. BRATERMAN, P. S. ORBITAL CORRELATION IN THE MAKING AND BREAKING OF TRANSITION METAL CARBON BONDS, P 149. TOPICS IN CURRENT CHEMIGTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  174480. GABRIEL WEATHERHEAD
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  174484. KAUFFMANN, T. IN SEARCH OF NEW ORGANOMETALLIC REAGENTS FOR ORGANIC SYNTHESIS, P 109. TOPICS IN CURRENT CHEMIGTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  174485. GABRIEL WEATHERHEAD
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  174489. HEIMBACH, P., SCHENKLUHN, H. CONTROLLING FACTORS IN HOMOGENOUS TRANSITION METAL CATALYSIS, P 45. TOPICS IN CURRENT CHEMIGTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  174490. GABRIEL WEATHERHEAD
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  174494. HUNIG, S. H.; BERNETH, H. TWO STEP REVERSIBLE REDOX SYSTEMS OF THE WEITZ TYPE, P 1. TOPICS IN CURRENT CHEMIGTRY (FORT. CHEM. FORSCHUNG), SPRINGER VERLAG: NEW YORK, 1980 A REVIEW.a
  174495. GABRIEL WEATHERHEAD
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  174499. ABBOUD, J. L. M., KAMLET, M. J.; TAFT, R. W. AN EXAMINATION OF LINEAR SOLVATION ENERGY RELATIONSHIPS, P 485. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174500. GABRIEL WEATHERHEAD
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  174504. RUNGE, W. SUBSTITUENT EFFECTS IN ALLENES AND CUMULENES, P 315. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174505. GABRIEL WEATHERHEAD
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  174509. STOCK, L. M.; WASIELEWSKI, M. R. THE TRIFLUOROMETHYL GROUP IN CHEMISTRY AND SPECTROSCOPY CARBON FLUORINE HYPERCONJUGATION, P 253. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.
  174510. GABRIEL WEATHERHEAD
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  174514. CHARTON, M. ELECTRICAL EFFECT SUBSTITUENT CONSTANTS FOR CORRELATION ANALYSIS, P 119. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174515. GABRIEL WEATHERHEAD
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  174519. GODLESKI, S. A.; SCHLEYER P. V R.; OSAWA, E.; WIPKE, W. T. THE SYSTEMATIC PREDICTION OF THE MOST STABLE NEUTRAL HYDROCARBON ISOMER, P 63. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174520. GABRIEL WEATHERHEAD
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  174524. PROSS, A.; RADOM, L. A THEORETICAL APPROACH TO SUBSTITUENT INTERACTIONS IN SUBSTITUTED BENZENES, P 1. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, VOL. 13, R. W. TAFT, ED., INTERSCIENCE: NEW YORK, 1981 A REVIEW.a
  174525. GABRIEL WEATHERHEAD
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  174529. HIGA, T. PHENOLIC SUBSTANCES. MARINE NATURAL PRODUCTS, VOL. 4, CHEMICAL AND BIOLOGICAL PERSPECTIVES, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  174530. GABRIEL WEATHERHEAD
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  174534. CHEVOLOT, L. GUANIDINE DERIVATIVES. MARINE NATURAL PRODUCTS, VOL. 4, CHEMICAL AND BIOLOGICAL PERSPECTIVES, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  174535. GABRIEL WEATHERHEAD
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  174539. MOORE, R. E. CONSTITUENTS OF BLUE GREEN ALGAE. MARINE NATURAL PRODUCTS, VOL. 4, CHEMICAL AND BIOLOGICAL PERSPECTIVES, P. J. SCHEUER, ED., ACADEMIC PRESS: NEW YORK, 1981 A REVIEW.a
  174540. GABRIEL WEATHERHEAD
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  174544. WILLIAMS, D. L. H.; BUNCEL, E. AROMATIC CATIONIC REACTIONS. ISOTOPES IN CATIONIC REACTIONS, VOL. 5, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
  174545. GABRIEL WEATHERHEAD
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  174549. ROBERTS, R. M., GIBSON, T. L. APPLICATIONS OF ISOTOPIC LABELING TO THE STUDY OF FRIEDEL CRAFTS REACTIONS. ISOTOPES IN CATIONIC REACTIONS, VOL. 5, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
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  174554. OAE, S.; NUMATA, T. THE PUMMERER AND PUMMERER TYPE OF REACTIONS. ISOTOPES IN CATIONIC REACTIONS, VOL. 5, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
  174555. GABRIEL WEATHERHEAD
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  174559. LEE, C. C. DEGENERATE REARRANGEMENTS IN TRIARYLVINYL CATIONS. ISOTOPES IN CATIONIC REACTIONS, VOL. 5, E. BUNCEL AND C. C. LEE, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
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  174564. STREITWIESER, JR., A.; JUARISTIE, E.; NEBENZAHL, L. L. EQUILIBRIUM CARBON ACIDITIES IN SOLUTION. COMPREHENSIVE CARBANION CHEMISTRY, PART A: STRUCTURE AND REACTIVITY, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
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  174589. PELLERITE, M. J.; BRAUMAN, J. I. GAS PHASE ACIDITIES OF CARBON ACIDS. COMPREHENSIVE CARBANION CHEMISTRY, PART A: STRUCTURE AND REACTIVITY, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
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  174594. BATES, R. B. DIANIONS AND POLYANIONS. COMPREHENSIVE CARBANION CHEMISTRY, PART A:STRUCTURE AND REACTIVITY, E. BUNCEL AND T. DURST, EDS., ELSEVIER: NEW YORK, 1980 A REVIEW.a
  174595. GABRIEL WEATHERHEAD
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  174599. MAZZOCCHI, P. H. THE PHOTOCHEMISTRY OF IMIDES, P 421. ORGANIC PHOTOCHEMISTRY, VOL. 5, A. PADWA, ED., DEKKER: NEW YORK, 1980 A REVIEW.a
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  174604. WEISS, D. S. THE NORRISH TYPE I REACTION IN CYCLOALKANONE PHOTOCHEMISTRY, P 347. ORGANIC PHOTOCHEMISTRY, VOL. 5, A. PADWA, ED., DEKKER: NEW YORK, 1980 A REVIEW.a
  174605. GABRIEL WEATHERHEAD
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  174609. GIVENS, R. S. PHOTOEXTRUSION OF SMALL MOLECULES, P 227. ORGANIC PHOTOCHEMISTRY, VOL. 5, A. PADWA, ED., DEKKER: NEW YORK, 1980 A REVIEW.a
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  174614. BALDWIN, S. W. SYNTHETIC ASPECTS OF 2 + 2 CYCLOADDITIONS OF A,B  UNSATURATED CARBONYL COMPOUNDS, P 123. ORGANIC PHOTOCHEMISTRY, VOL. 5, A. PADWA, ED., DEKKER: NEW YORK, 1980 A REVIEW.a
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  174619. JONES, II, G. SYNTHETIC APPLICATIONS OF THE PATERNO BUCHI REACTION, P 1. ORGANIC PHOTOCHEMISTRY, VOL. 5, A. PADWA, ED., DEKKER: NEW YORK, 1980 A REVIEW.a
  174620. GABRIEL WEATHERHEAD
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  174624. AYER, W. A.; BROWNE, L. M. TERPENOID METABOLITES OF MUSHROOMS AND RELATED BASIDIOMYCETES. 1981, 37, 2199. TETRAHEDRON A REVIEW.a
  174625. GABRIEL WEATHERHEAD
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  174628. 2/28/96VgWASSERMAN, H. H.; IVES, J. L. SINGLET OXYGEN IN ORGANIC SYNTHESIS. 1981, 37,1825. TETRAHEDRON A REVIEW.a
  174629. GABRIEL WEATHERHEAD
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  174632. 2/28/96VOWALBORSKY, H. M. THE CYCLOPROPYL RADICAL. 1981, 37, 1625. TETRAHEDRON A REVIEW.a
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  174636. 2/28/96VoRAJAPPA, S. NITROENAMINES. PREPARATION, STRUCTURE AND SYNTHETIC POTENTIAL. 1981, 37,1453. TETRAHEDRON A REVIEW.a
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  174641. KROW, G. R. NITROGEN INSERTION REACTIONS OF BRIDGED BICYCLIC KETONES. REGIOSELECTIVE LACTAM FORMATION. 1981, 37, 1283. TETRAHEDRON A REVIEW.a
  174642. GABRIEL WEATHERHEAD
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  174645. 2/28/96VqHUTCHINSON C. R. CAMPTOTHECIN: CHEMISTRY, BIOGENESIS AND MEDICINAL CHEMISTRY. 1981 37,1047. TETRAHEDRON A REVIEW.
  174646. GABRIEL WEATHERHEAD
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  174649. 2/28/96VcRIDDELL, F. G. THE CONFORMATIONS OF HYDROXYLAMINE DERIVATIVES. 1981, 37, 849. TETRAHEDRON A REVIEW.a
  174650. GABRIEL WEATHERHEAD
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  174654. FRECHET, J. M. J. SYNTHESIS AND APPLICATIONS OF ORGANIC POLYMERS AS SUPPORTS AND PROTECTING GROUPS. 1981, 37, 663. TETRAHEDRON A REVIEW.a
  174655. GABRIEL WEATHERHEAD
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  174658. 2/28/96V|GOLOLOBOV, YU. G.; ZHMUROVA, I. N.; KASUKHIN, L. F. SIXTY YEARS OF STAUDINGER REACTION. 1981, 37, 437. TETRAHEDRON A REVIEW.a
  174659. GABRIEL WEATHERHEAD
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  174662. 2/28/96VyMIKOYAJCZYK, M.; KIEYBASINSKI, P. RECENT DEVELOPMENTS IN THE CARDODIIMIDE CHEMISTRY. 1981, 37, 233. TETRAHEDRON A REVIEW.a
  174663. GABRIEL WEATHERHEAD
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  174667. KAMETANI, T., NEMOTO, H. RECENT ADVANCES IN THE TOTAL SYNTHESIS OF STEROIDS VIA INTRAMOLECULAR CYCLOADDITION REACTIONS. 1981, 37, 3. TETRAHEDRON A REVIEW.a
  174668. GABRIEL WEATHERHEAD
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  174671. 2/28/96VkJOHNSON, C. D. THE REACTIVITY SELECTIVITY PRINCIPLE: FACT OR FICTION? 1980, 36, 3461. TETRAHEDRON A REVIEW.a
  174672. GABRIEL WEATHERHEAD
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  174676. BOSNICH, B., FRYZUK, M. D. ASYMMETRIC SYNTHESIS MEDIATED BY TRANSITION METAL COMPLEXES. 1981,12,119. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  174677. GABRIEL WEATHERHEAD
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  174681. FLOOD, T. C. STEREOCHEMISTRY OF REACTIONS OF TRANSITION METAL CARBON SIGMA BONDS. 1981,12, 37. TOPICS IN STEREOCHEMISTRY A REVIEW.a
  174682. GABRIEL WEATHERHEAD
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  174685. 2/28/96VhAKELAH, A. HETEROGENEOUS ORGANIC SYNTHESIS USING FUNCTIONALIZED POLYMERS. 1981, 413. SYNTHESIS A REVIEW.a
  174686. GABRIEL WEATHERHEAD
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  174689. 2/28/96V_BODANSZKY, M.; MARTINEZ, J. SIDE REACTIONS IN PEPTIDE SYNTHESIS. 1981, 333. SYNTHESIS A REVIEW.a
  174690. GABRIEL WEATHERHEAD
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  174693. 2/28/96VRALBINI, A. PHOTOSENSITIZATION IN ORGANIC SYNTHESIS. 1981, 249. SYNTHESIS A REVIEW.
  174694. GABRIEL WEATHERHEAD
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  174698. SOLLADIE, G. ASYMMETRIC SYNTHESIS USING NUCLEOPHILIC REAGENTS CONTAINING A CHIRAL SULFOXIDE GROUP. 1981,185. SYNTHESIS A REVIEW.a
  174699. GABRIEL WEATHERHEAD
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  174702. 2/28/96VtMANCUSO, A. J.; SWERN, D. ACTIVATED DIMETHYL SULFOXIDE: USEFUL REAGENTS FOR SYNTHESIS. 1981,165. SYNTHESIS A REVIEW.a
  174703. GABRIEL WEATHERHEAD
  174704. 11605
  174705. 12614N
  174706. 2/28/96VdCAPLAR, V.; COMISSO, G.; SUNJIC. HOMOGENEOUS ASYMMETRIC HYDROGENATION. 1981, 85. SYNTHESIS A REVIEW.a
  174707. GABRIEL WEATHERHEAD
  174708. 11606
  174709. 12615N
  174710. 2/28/96V
  174711. MITSUNOBU, O. THE USE OF DIETHYL AZODICARBOXYLATE AND TRIPHENYLPHOSPHINE IN SYNTHESIS AND TRANSFORMATION OF NATURAL PRODUCTS. 1981,1. SYNTHESIS A REVIEW.a
  174712. GABRIEL WEATHERHEAD
  174713. 11607
  174714. 12616N
  174715. 2/28/96V
  174716. FRIDMAN, A. L.; SURKOV, V. D.; NOVIKOV, S. S. CHEMISTRY OF A HALOGENONITROALKANES. 1980, 49,1068. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174717. GABRIEL WEATHERHEAD
  174718. 11608
  174719. 12617N
  174720. 2/28/96V
  174721. GENOKHOVA, N. S., MELENT'EVA, T. A., BEREZOVSKII, V. M. SYNTHESIS OF CORROLES AND OCTADEHYDROCORRINS. 1980, 49, 1056. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174722. GABRIEL WEATHERHEAD
  174723. 11609
  174724. 12618N
  174725. 2/28/96V
  174726. DYUMAEV, K. M., KOROLEV, B. A. THE INFLUENCE OF SOLVATION ON THE ACID BASE PROPERTIES OF ORGANIC COMPOUNDS IN VARIOUS MEDIA. 1980, 49,1021. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174727. GABRIEL WEATHERHEAD
  174728. 11610
  174729. 12619N
  174730. 2/28/96V
  174731. GALISHEV, V. A., CHISTOKLETOV, V. N.; PETROV, A. A. .A,B UNSATURATED HETEROATOMIC COMPOUNDS IN 1,3 DIPOLAR ADDITION REACTIONS. 1980, 49, 880. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174732. GABRIEL WEATHERHEAD
  174733. 11611
  174734. 12620N
  174735. 2/28/96VdKARAEV, S. F.; GARAEVA, SH. V. PROP 2 YNYL ETHERS. 1980, 49, 865. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174736. GABRIEL WEATHERHEAD
  174737. 11612
  174738. 12621N
  174739. 2/28/96
  174740. KREITSBERGA, YA. N.; NEILAND, O. YA. ARYLATED CYCLOPENTADIENES AND CYCLOPENTADIENYLIDES. 1980, 49, 854. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174741. GABRIEL WEATHERHEAD
  174742. 11613
  174743. 12622N
  174744. 2/28/96V
  174745. ZHDANOV, YU. A., UZLOVA, L. A.; GLEBOVA, Z. I. A KETOPHOSPHONIC ACID ESTERS
  174746. SYNTHESIS, STRUCTURE, AND REACTIONS. 1980, 49, 843. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174747. GABRIEL WEATHERHEAD
  174748. 11614
  174749. 12623N
  174750. 2/28/96VtYABLOKOV, V. A. THE MECHANISMS OF THE REARRANGEMENTS OF PEROXIDES. 1980, 49, 833. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174751. GABRIEL WEATHERHEAD
  174752. 11615
  174753. 12624N
  174754. 2/28/96V
  174755. TOLKACHEV, O. N.; NAKOVA, E. P.; EVSTIGNEEVA, R. P. SYNTHESIS OF BISBENZYLISOQUINOLINE ALKALOIDS. 1980, 49, 784. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174756. GABRIEL WEATHERHEAD
  174757. 11616
  174758. 12625N
  174759. 2/28/96V
  174760. MUKHAMETSHIN, F. M. ADVANCES IN THE CHEMISTRY OF ORGANOFLUORINE HYPOHALITES AND RELATED COMPOUNDS. 1980, 49, 668. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174761. GABRIEL WEATHERHEAD
  174762. 11617
  174763. 12626N
  174764. 2/28/96VnKHALDNA, YU. L. METHODS OF CALCULATING PKBH+ FOR WEAK BASES. 1980, 49, 623. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174765. GABRIEL WEATHERHEAD
  174766. 11618
  174767. 12627N
  174768. 2/28/96V
  174769. KHOMENKO, T. I., SAKHNROV, M. M.; GOLOVINA, O. A. THE SYNTHESIS OF CARBOHYDRATES FROM FORMALDEHYDE. 1980, 49, 570. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174770. GABRIEL WEATHERHEAD
  174771. 11619
  174772. 12628N
  174773. 2/28/96V
  174774. AKSENOV, V. S.; TERENT'EVA, G. A.; SAVINYKH, YU. V. NUCLEOPHILIC SUBSTITUTION REACTIONS OF CYCLOPROPANE DERIVATIVES. 1980, 49, 549. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174775. GABRIEL WEATHERHEAD
  174776. 11620
  174777. 12629N
  174778. 2/28/96V
  174779. LYAPINA, N. K.; LYGIN, V. I.; ULENDEEVA, A. D. MECHANISM OF THE ADSORPTION OF ORGANIC SULFUR COMPOUNDS BY OXIDES AND ZEOLITES. 1980, 49, 526. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174780. GABRIEL WEATHERHEAD
  174781. 11621
  174782. 12630N
  174783. 2/28/96
  174784. V|LAKHONTOV, L. N.; PROKOPOV, A. A. ADVANCES IN THE CHEMISTRY OF AZAINDOLES. 1980, 49, 428. RUSSIAN CHEMICAL REVIEWS A REVIEW.a
  174785. GABRIEL WEATHERHEAD
  174786. 11622
  174787. 12631N
  174788. 2/28/96VxLENZ, G. R. PHOTOCYCLOADDITION REACTIONS OF CONJUGATED ENONES. 1981, 4, 369. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174789. GABRIEL WEATHERHEAD
  174790. 11623
  174791. 12632N
  174792. 2/28/96V^COLEMAN, B.; JONES, JR., M. SILENES. 1981, 4, 297. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174793. GABRIEL WEATHERHEAD
  174794. 11624
  174795. 12633N
  174796. 2/28/96VvSODEAU, J. R.; LEE, E. K. C. PHOTOREACTIONS OF FORMALDEHYDE. 1981, 4, 259. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174797. GABRIEL WEATHERHEAD
  174798. 11625
  174799. 12634N
  174800. 2/28/96VuLAUFER, A. H. KINETICS OF GAS PHASE REACTIONS OF METHYLENE. 1981, 4, 225. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174801. GABRIEL WEATHERHEAD
  174802. 11626
  174803. 12635N
  174804. 2/28/96
  174805. MOGGI, L.; JURIS, A.; SANDRINI, D.; MANFRIN, M. F. PHOTOCATALYSIS BY TRANSITION METAL COORDINATION COMPOUNDS IN HOMOGENEOUS PHASE. 1981, 4,171. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174806. GABRIEL WEATHERHEAD
  174807. 11627
  174808. 12636N
  174809. 2/28/96V
  174810. DE VIOLET, PH. F. POLYHALIDE RADICAL ANIONS AS INTERMEDIATES IN CHEMISTRY. 1981, 4,121. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174811. GABRIEL WEATHERHEAD
  174812. 11628
  174813. 12637N
  174814. 2/28/96V
  174815. LEONE, A. A.; MARIANO, P. S. THE PHOTOCHEMISTRY OF 3 HETEROATOM SUBSTITUTED 1,4 DIENES. 1981, 4, 81. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174816. GABRIEL WEATHERHEAD
  174817. 11629
  174818. 12638N
  174819. 2/28/96V
  174820. PARK, S. M.; TRYK, D. A. EXCITED STATE INTERMEDIATES PROBED BY ELECTROGENERATED CHEMILUMINESCENCE. 1981, 4, 43. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174821. GABRIEL WEATHERHEAD
  174822. 11630
  174823. 12639N
  174824. 2/28/96
  174825. STEER, R. P. STRUCTURE AND DECAY DYNAMICS OF ELECTRONIC EXCITED STATES OF THIOCARBONYL COMPOUNDS. 1981, 4, 1. REVIEWS OF CHEMICAL INTERMEDIATES A REVIEW.a
  174826. GABRIEL WEATHERHEAD
  174827. 11631
  174828. 12640N
  174829. 2/28/96V
  174830. BUCK, H. M. MECHANISTIC ASPECTS OF ORGANOPHOSPHORUS CHEMISTRY. 1981,100, 217. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS A REVIEW.a
  174831. GABRIEL WEATHERHEAD
  174832. 11632
  174833. 12641N
  174834. 2/28/96V
  174835. VERHOEVEN, J. W. SIGMA ASSISTANCE; THE MODULATION OF INTRAMOLECULAR REACTIVITY BY THROUGH BOND INTERACTION. 1980, 99, 369. RECUEIL DES TRAVAUX CHIMIQUES DES PAYS BAS A REVIEW.a
  174836. GABRIEL WEATHERHEAD
  174837. 11633
  174838. 12642N
  174839. 2/28/96V
  174840. INAGAKI, F.; MIYAZAWA, T. NMR ANALYSES OF MOLECULAR CONFORMATIONS AND CONFORMATIONAL EQUILIBRIA WITH THE LANTHANIDE PROBE METHOD. 1981,14, 67. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY A REVIEW.a
  174841. GABRIEL WEATHERHEAD
  174842. 11634
  174843. 12643N
  174844. 2/28/96
  174845. JEFFORD, C. W.; CADBY, P. A. MOLECULAR MECHANISMS OF ENZYME CATALYZED DIOXYGENATION. (AN INTERDISCIPLINARY REVIEW.) 1981, 40, 191. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  174846. GABRIEL WEATHERHEAD
  174847. 11635
  174848. 12644N
  174849. 2/28/96V
  174850. COOKE, R. G.; EDWARDS J. M. NATURALLY OCCURRING PHENALENONES AND RELATED COMPOUNDS. 1981, 40, 153. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  174851. GABRIEL WEATHERHEAD
  174852. 11636
  174853. 12645N
  174854. 2/28/96V
  174855. HELLER, W., TAMM, CH. HOMOISOFLAVANONES AND BIOGENETICALLY RELATED COMPOUNDS. 1981, 40,105. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  174856. GABRIEL WEATHERHEAD
  174857. 11637
  174858. 12646N
  174859. 2/28/96V
  174860. DEV, S. THE CHEMISTRY OF LONGIFOLENE AND ITS DERIVATIVES. 1981, 40, 49. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  174861. GABRIEL WEATHERHEAD
  174862. 11638
  174863. 12647N
  174864. 2/28/96
  174865. LEFRANCIER, P.; LEDERER, E. CHEMISTRY OF SYNTHETIC IMMUNOMODULANT MURAMYL PEPTIDES. 1981, 40, 1. PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS A REVIEW.a
  174866. GABRIEL WEATHERHEAD
  174867. 11639
  174868. 12648N
  174869. 2/28/96V`QUINIOU, H. THIOAMIDE VINYLOGS. 1981,10, 1. PHOSPHORUS AND SULFUR AND RELATED ELEMENTS A REVIEW.a
  174870. GABRIEL WEATHERHEAD
  174871. 11640
  174872. 12649N
  174873. 2/28/96V
  174874. TODRES, Z. V. THE ROLE OF THE ELECTRON TRANSFER STAGE IN REACTIONS OF ORGANOSULFUR COMPOUMDS AND THE PROBLEM OF DIRECTED INFLUENCE ON THESE REACTIONS 1981, 9, 353. PHOSPHORUS AND SULFUR AND RELATED ELEMENTS A REVIEW.a
  174875. GABRIEL WEATHERHEAD
  174876. 11641
  174877. 12650N
  174878. 2/28/96V
  174879. ABEL, E. W.; MUCKLEJOHN, S. A. THE CHEMISTRY OF PHOSPHINIMINES. 1981, 9, 235. PHOSPHORUS AND SULFUR AND RELATED ELEMENTS A REVIEW.a
  174880. GABRIEL WEATHERHEAD
  174881. 11642
  174882. 12651N
  174883. 2/28/96
  174884. DE KIMPE, N.; SCHAMP, N. THE SYNTHESIS OF  ALPHA HALOGENATED ENAMINES. 1981,13, 241. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174885. GABRIEL WEATHERHEAD
  174886. 11643
  174887. 12652N
  174888. 2/28/96V
  174889. HUTCHINS, R. O.  CISTONE, F. UTILITY AND APPLICATIONS OF BORANE DIMETHYLSULFIDE IN ORGANIC SYNTHESIS. 1981,13, 225. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174890. GABRIEL WEATHERHEAD
  174891. 11644
  174892. 12653N
  174893. 2/28/96V
  174894. IKAN, R., WEINSTEIN, V., RAVID, U. SYNTHESIS OF SATURATED  GAMMA LACTONES. 1981,13, 59ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174895. GABRIEL WEATHERHEAD
  174896. 11645
  174897. 12654N
  174898. 2/28/96V
  174899. LAI, Y. H. ORGANIC REDUCTIVE COUPLING WITH TITANIUM  AND VANADIUM CHLORIDES. 1980,12, 361. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174900. GABRIEL WEATHERHEAD
  174901. 11646
  174902. 12655N
  174903. 2/28/96V}MATHIAS, L. J. SYNTHETIC APPLICATIONS OF ISOUREAS. 1980, 12, 309. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.
  174904. GABRIEL WEATHERHEAD
  174905. 11647
  174906. 12656N
  174907. 2/28/96V
  174908. DE KIMPE, N.; VERHE, R., DE BUYCK, L., SCHAMP, N. REACTIVITY OF A HALOGENATED IMINO COMPOUNDS. 1980,12, 49. A REVIEW. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174909. GABRIEL WEATHERHEAD
  174910. 11648
  174911. 12657N
  174912. 2/28/96VqNAGAI, Y. HYDROSILANES AS REDUCING AGENTS. 1980,12,13 ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL A REVIEW.a
  174913. GABRIEL WEATHERHEAD
  174914. 11649
  174915. 12658N
  174916. 2/28/96V
  174917. FRIEDRICHSEN, W.; BOTTCHER, A. RECENT DEVELOPMENTS IN THE CHEMISTRY OF O BENZOQUINONE DIIMINES. 1981,16,1009. HETEROCYCLES A REVIEW.a
  174918. GABRIEL WEATHERHEAD
  174919. 11650
  174920. 12659N
  174921. 2/28/96VkSARAF, S. U. D. ABSORPTION SPECTRA OF BENZOLOGS OF QUINOLIZINIUM IONS. 1981,16, 987. HETEROCYCLES A REVIEW.a
  174922. GABRIEL WEATHERHEAD
  174923. 11651
  174924. 12660N
  174925. 2/28/96VsSARAF, S. U. D. THE CHEMISTRY OF THE BENZO[A]  AND BENZO[C]QUINOLIZINIUM IONS. 1981,16, 803. HETEROCYCLES A REVIEW.a
  174926. GABRIEL WEATHERHEAD
  174927. 11652
  174928. 12661N
  174929. 2/28/96V
  174930. PANDEY, G. D.; TIWARI, K. P. ON THE USE OF LACTONES AS BUILDING BLOCKS IN THE ALKALOID SYNTHESIS
  174931. A REVIEW. 1981, 16, 449. HETEROCYCLES A REVIEW.a
  174932. GABRIEL WEATHERHEAD
  174933. 11653
  174934. 12662N
  174935. 2/28/96VsDOLPHIN, D.; HIOM, J.; PAINE III, J. B. COVALENTLY LINKED DIMERIC PORPHYRINS. 1981, 16, 417. HETEROCYCLES A REVIEW.a
  174936. GABRIEL WEATHERHEAD
  174937. 11654
  174938. 12663N
  174939. 2/28/96V
  174940. KOZIKOWSKI, A. P. SYNTHESIS OF 4 SUBSTITUTED INDOIES AND THEIR ELABORATION TO THE ERGOT ALKALOIDS. 1981,16 267. HETEROCYCLES A REVIEW.a
  174941. GABRIEL WEATHERHEAD
  174942. 11655
  174943. 12664N
  174944. 2/28/96V
  174945. MUKAI, T.; KUMAGAI, T.; YAMASHITA, Y. CYCLIZATION AND CYCLOADDITION REACTIONS OF HETEROEPINS, CONJUGATED SEVEN MEMBERED HETEROCYCLIC COMPOUNDS. 1981, 15 1569. HETEROCYCLES A REVIEW.a
  174946. GABRIEL WEATHERHEAD
  174947. 11656
  174948. 12665N
  174949. 2/28/96V
  174950. NOMURA, T., FUKAI, T. PRENYLFLAVONOIDS FROM THE ROOT BARK OF THE CULTIVATED MULBERRY TREE. 1981, 15, 1531. HETEROCYCLES A REVIEW.
  174951. GABRIEL WEATHERHEAD
  174952. 11657
  174953. 12666N
  174954. 2/28/96VgSANTAVY, F. ALKALOIDS FROM PLANTS OF THE SUBFAMILY WURMBAEOIDEAE. 1981,15, 1505. HETEROCYCLES A REVIEW.a
  174955. GABRIEL WEATHERHEAD
  174956. 11658
  174957. 12667N
  174958. 2/28/96VWPIOZZI, F. THE DITERPENOIDS OF TEUCRIUM SPECIES. 1981, 15, 1489. HETEROCYCLES A REVIEW.a
  174959. GABRIEL WEATHERHEAD
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  174961. 12668N
  174962. 2/28/96V
  174963. NINOMIYA, I.; NAITO, T. ENAMIDE PHOTOCYCLIZATION AND ITS APPLICATION TO THE SYNTHESIS OF HETEROCYCLES. 1981,15, 1433. HETEROCYCLES A REVIEW.a
  174964. GABRIEL WEATHERHEAD
  174965. 11660
  174966. 12669N
  174967. 2/28/96VVKUTNEY, J. P. STUDIES ON PLANT TISSUE CULTURES. 1981, 15, 1405. HETEROCYCLES A REVIEW.a
  174968. GABRIEL WEATHERHEAD
  174969. 11661
  174970. 12670N
  174971. 2/28/96V
  174972. DAUKSAS, V. K.; PURVANECKAS, G. V.; UDENAITE, E. B. GINEITYTE, V. L.; BARAUSKAITE, A. V. RELATIVE REACTIVITY OF THE AROMATIC RING IN BENZO 1,3 DIOXOLE, ITS CYCLOHOMOLOGUES AND VERATROLE. 1981,15,1395. HETEROCYCLES A REVIEW.a
  174973. GABRIEL WEATHERHEAD
  174974. 11662
  174975. 12671N
  174976. 2/28/96V
  174977. UNDHEIM, K. THE NOVEL DIHYDROTHIAZOLO[3,2 A]PYRIDINIUM 8 OLATE AND CLOSELY RELATED SYSTEMS; SYNTHESES AND REACTIONS. 1981,15,1349. HETEROCYCLES A REVIEW.a
  174978. GABRIEL WEATHERHEAD
  174979. 11663
  174980. 12672N
  174981. 2/28/96VxOKUDA, T.; YOSHIDA, T., MORI, K., HATANO, T. TANNINS OF MEDICINAL PLANTS AND DRUGS. 1981,15,1323. HETEROCYCLES A REVIEW.a
  174982. GABRIEL WEATHERHEAD
  174983. 11664
  174984. 12673N
  174985. 2/28/96VaJOSHI, B. S. RECENT CHEMISTRY OF SOME INDIAN PIPER SPECIES. 1981,15, 1309. HETEROCYCLES A REVIEW.a
  174986. GABRIEL WEATHERHEAD
  174987. 11665
  174988. 12674N
  174989. 2/28/96V
  174990. KLEMM, L. H. A CORRELATION OF THE CHEMISTRIES OF TWO THIENOPYRIDINES AND THOSE OF BENZO[B]THIOPHENE AND QUINOLINE. 1981,15, 1285. HETEROCYCLES A REVIEW.a
  174991. GABRIEL WEATHERHEAD
  174992. 11666
  174993. 12675N
  174994. 2/28/96VWSCOTT A. I., ET AL. INDOLE ALKALOID BIOSYNTHESIS. 1981 15, 1257. HETEROCYCLES A REVIEW.a
  174995. GABRIEL WEATHERHEAD
  174996. 11667
  174997. 12676N
  174998. 2/28/96
  174999. VbFUNAYAMA, S.; HIKINO, H. HYPOTENSIVE PRINCIPLES FROM PLANTS. 1981,15, 1239. HETEROCYCLES A REVIEW.a
  175000. GABRIEL WEATHERHEAD
  175001. 11668
  175002. 12677N
  175003. 2/28/96VpFLEMING, I. SOME USES OF SILICON COMPOUNDS IN ORGANIC SYNTHESIS. 1981,10, 83. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  175004. GABRIEL WEATHERHEAD
  175005. 11669
  175006. 12678N
  175007. 2/28/96VkBIRD, C. L.; KUHN, A. T. ELECTROCHEMISTRY OF THE VIOLOGENS. 1981,10, 49. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  175008. GABRIEL WEATHERHEAD
  175009. 11670
  175010. 12679N
  175011. 2/28/96VnKENNEWELL, P. D.; TAYLOR, J. B. THE SULPHOXIMIDES: AN UPDATE. 1980, 9, 477. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  175012. GABRIEL WEATHERHEAD
  175013. 11671
  175014. 12680N
  175015. 2/28/96VqLYTHGOE, B. SYNTHETIC APPROACHES TO VITAMIN D AND ITS RELATIVES. 1980, 9, 449. CHEMICAL SOCIETY REVIEWS A REVIEW.a
  175016. GABRIEL WEATHERHEAD
  175017. 11672
  175018. 12681N
  175019. 2/28/96
  175020. SINGH, S. P.; PARMAR, S. S.; RAMAN, K.; STENBERG, V. I.  CHEMISTRY AND BIOLOGICAL ACTIVITY OF THIAZOLIDINONES. 1981, 81, 175. CHEMICAL REVIEWS A REVIEW.a
  175021. GABRIEL WEATHERHEAD
  175022. 11673
  175023. 12682N
  175024. 2/28/96VmJEYARAMAN, R.; AVILA, S. CHEMISTRY OF 3 AZABICYCLO   [3.3.1]NONANES. 1981, 81,149. CHEMICAL REVIEWS A REVIEW.a
  175025. GABRIEL WEATHERHEAD
  175026. 11674
  175027. 12683N
  175028. 2/28/96VgBALCI, M. BICYCLIC ENDOPEROXIDES AND SYNTHETIC APPLI  CATIONS. 1981, 81, 91. CHEMICAL REVIEWS A REVIEW.a
  175029. GABRIEL WEATHERHEAD
  175030. 11675
  175031. 12684N
  175032. 2/28/96V}KOMECZNY, M., SOSNOVSKY, G. CHEMISTRY OF ORGANO PHOSPHORUS COMPOUNDS CONTAINING THE PEROXIDE BOND. CHEMICAL REVIEWS A REVIEW.a
  175033. GABRIEL WEATHERHEAD
  175034. 11676
  175035. 12685N
  175036. 2/28/96V
  175037. SCHILDKNECHT, H. IRRITANT AND DEFENSE SUBSTANCES OF HIGHER PLANTS
  175038. A CHEMICAL HERBARIUM. 1981, 20, 164. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  175039. GABRIEL WEATHERHEAD
  175040. 11677
  175041. 12686N
  175042. 2/28/96
  175043. HAMPRECHT, G.; KONIG, K. H.; STUBENRAUCH, G. ALKYLSULFAMOYL CHLORIDES AS KEY UNITS IN THE SYNTHESIS OF NOVEL BIOLOGICALLY ACTIVE COMPOUNDS FOR CROP PROTECTION. 1981, 20, 151. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  175044. GABRIEL WEATHERHEAD
  175045. 11678
  175046. 12687N
  175047. 2/28/96V
  175048. REICHERT, D. TOXICATION OF FOREIGN SUBSTANCES BY CONJUGATION REACTIONS. 1981, 20,135. ANGEWANDTE CHEMIE, INTERNATIONAL EDITION IN ENGLISH A REVIEW.a
  175049. GABRIEL WEATHERHEAD
  175050. 11679
  175051. 12688N
  175052. 2/28/96V
  175053. SCHMIDT, A. H. BROMOTRIMETHYLSILANE AND IODOTRIMETHYLSILANE
  175054. VERSATILE REAGENTS FOR ORGANIC SYNTHESIS. 1981, 14, 31. ALDRICHIMICA ACTA A REVIEW.a
  175055. GABRIEL WEATHERHEAD
  175056. 11680
  175057. 12689N
  175058. 2/28/96VFDAWSON D. J. POLYMERIC DYES. 1981, 14, 23. ALDRICHIMICA ACTA A REVIEW.a
  175059. GABRIEL WEATHERHEAD
  175060. 11681
  175061. 12690N
  175062. 2/28/96V
  175063. BROWN, H. C., CAMPBELL, J. B., JR. SYNTHESIS AND APPLICATIONS OF VINYLIC ORGANOBORANES. 1981,14, 3. ALDRICHIMICA ACTA A REVIEW.
  175064. GABRIEL WEATHERHEAD
  175065. 11682
  175066. 12691N
  175067. 2/28/96V
  175068. KUNITAKE, T.; SHINKAI, S. CATALYSIS BY MICELLES, MEMBRANES AND OTHER AQUEOUS AGGREGATES AS MODELS OF ENZYME ACTION. 1981,1 7, 435. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  175069. GABRIEL WEATHERHEAD
  175070. 11683
  175071. 12692N
  175072. 2/28/96V
  175073. DE JONG, F.; REINHOUDT, D. N. STABILITY AND REACTIVITY OF CROWN ETHER COMPLEXES. 1981,17, 279. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  175074. GABRIEL WEATHERHEAD
  175075. 11684
  175076. 12693N
  175077. 2/28/96V
  175078. KIRBY, A. J. EFFECTIVE MOLARITIES FOR INTRAMOLECULAR REACTIONS. 1981, 17, 183. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  175079. GABRIEL WEATHERHEAD
  175080. 11685
  175081. 12694N
  175082. 2/28/96V
  175083. KICE, J. L. MECHANISMS AND REACTIVITY OF ORGANIC OXYACIDS OF SULFUR AND THEIR ANHYDRIDES. 1981,17, 65. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  175084. GABRIEL WEATHERHEAD
  175085. 11686
  175086. 12695N
  175087. 2/28/96
  175088. VYPERKINS, M. J. SPIN TRAPPING. 1981,17,1. ADVANCES IN PHYSICAL ORGANIC CHEMISTRY A REVIEW.a
  175089. GABRIEL WEATHERHEAD
  175090. 11687
  175091. 12696N
  175092. 2/28/96V
  175093. JOLLY, P. W., MYNOTT, R. THE APPLICATION OF 13C NMR SPECTROSCOPY TO ORGANO TRANSITION METAL COMPLEXES. 1981, 19, 257. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175094. GABRIEL WEATHERHEAD
  175095. 11688
  175096. 12697N
  175097. 2/28/96V
  175098. CURTIS, M. D.; EPSTEIN, P. S. REDISTRIBUTION REACTIONS ON SILICON CATALYZED BY TRANSITION METAL COMPLEXES. 1981, 19, 213 ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175099. GABRIEL WEATHERHEAD
  175100. 11689
  175101. 12698N
  175102. 2/28/96V|ALPER, H. PHASE TRANSFER CATALYSIS IN ORGANOMETALLIC CHEMISTRY. 1981,19, 183. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175103. GABRIEL WEATHERHEAD
  175104. 11690
  175105. 12699N
  175106. 2/28/96V
  175107. WERNER, H. NOVEL TYPES OF METAL METAL BONDED COMPLEXES CONTAINING ALLYL AND CYCLOPENTADIENYL BRIDGING LIGANDS. 1981,19, 155. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175108. GABRIEL WEATHERHEAD
  175109. 11691
  175110. 12700N
  175111. 2/28/96V
  175112. CONNOLLY, J. W.; HOFF, C. ORGANIC COMPOUNDS OF DIVALENT TIN AND LEAD. 1981,19,123. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175113. GABRIEL WEATHERHEAD
  175114. 11692
  175115. 12701N
  175116. 2/28/96VrJONAS, K. ALKALI METAL TRANSITION METAL PI COMPLEXES. 1981, 19, 97. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175117. GABRIEL WEATHERHEAD
  175118. 11693
  175119. 12702N
  175120. 2/28/96VyISHIKAWA, M.; KUMADA, M. PHOTOCHEMISTRY OF ORGANOPOLYSILANES. 1981,19, 51. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175121. GABRIEL WEATHERHEAD
  175122. 11694
  175123. 12703N
  175124. 2/28/96V|PEZ, G. P.; ARMOR, J. N. CHEMISTRY OF TITANOCENE AND ZIRCONOCENE. 1981,19, 2. ADVANCES IN ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175125. GABRIEL WEATHERHEAD
  175126. 11695
  175127. 12704N
  175128. 2/28/96VkGRIMMETT, M. R. ADVANCES IN IMIDAZOLE CHEMISTRY. 1981 27, 242. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  175129. GABRIEL WEATHERHEAD
  175130. 11696
  175131. 12705N
  175132. 2/28/96
  175133. %VuLOZAC'H N.; STAVAUX, M. THE 1,2  AND 1,3 DITHIOLIUM LONS. 1981, 27, 152. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  175134. GABRIEL WEATHERHEAD
  175135. 11697
  175136. 12706N
  175137. 2/28/96V
  175138. HANSON, P. HETEROAROMATIC RADICALS, PART II: RADICALS WITH GROUP VL AND GROUPS V AND VI RING HETEROATOMS. 1981, 27, 32. ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  175139. GABRIEL WEATHERHEAD
  175140. 11698
  175141. 12707N
  175142. 2/28/96V
  175143. BLACK, D. ST. C.; DOYLE, J. E. L AZABICYCLO[3.1.0]HEXANES AND ANALOGS WITH FURTHER HETEROATOM SUBSTITUTION. 1981, ADVANCES IN HETEROCYCLIC CHEMISTRY A REVIEW.a
  175144. GABRIEL WEATHERHEAD
  175145. 11699
  175146. 12708N
  175147. 2/28/96V
  175148. UNGER, F. D. THE CHEMISTRY AND BIOLOGICAL SIGNIFICANCE OF 3 DEOXY D MANNO 2 OCTULOSONIC ACID (KDO). 1981, 37, 323. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  175149. GABRIEL WEATHERHEAD
  175150. 11700
  175151. 12709N
  175152. 2/28/96
  175153. CRAWFORD, T. C. THE GULONO 1,4 LACTONES: A REVIEW OF THEIR SYNTHESIS, REACTIONS, AND RELATED DERIVATIVES. 1981, 37, 287. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  175154. GABRIEL WEATHERHEAD
  175155. 11701
  175156. 12710N
  175157. 2/28/96VtPENGLIS, A. A. E. FLUORINATED CARBOHYDRATES. 1981, 37, ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  175158. GABRIEL WEATHERHEAD
  175159. 11702
  175160. 12711N
  175161. 2/28/96V
  175162. BINKLEY, R. W. PHOTOCHEMICAL REACTIONS OF CARBOHYDRATES. 1981, 37, 105. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  175163. GABRIEL WEATHERHEAD
  175164. 11703
  175165. 12712N
  175166. 2/28/96V
  175167. GORIN, P. A. J. CARBON 13 NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY OF POLYSACCHARIDES. 1981, 37,13. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY A REVIEW.a
  175168. GABRIEL WEATHERHEAD
  175169. 11704
  175170. 12713N
  175171. 2/28/96
  175172. DEPUY, C. H., BIERBAUM, V. M. GAS PHASE REACTIONS OF ORGANIC ANIONS AS STUDIES BY THE FLOWING AFTERGLOW TECHNIQUE. 1981,14, 146. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175173. GABRIEL WEATHERHEAD
  175174. 11705
  175175. 12714N
  175176. 2/28/96VsNELSEN, S. F. ONE ELECTRON OXIDATION OF TETRAALKYLHYDRAZINES. 1981,14, 131. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175177. GABRIEL WEATHERHEAD
  175178. 11706
  175179. 12715N
  175180. 2/28/96VpLUKEHART, C. M. METALLA B DIKETONES AND THEIR DERIVATIVES. 1981,14, 109. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175181. GABRIEL WEATHERHEAD
  175182. 11707
  175183. 12716N
  175184. 2/28/96VpTRAYLOR, T. G. SYNTHETIC MODEL COMPOUNDS FOR HEMOPROTEINS. 1981,14, 102. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175185. GABRIEL WEATHERHEAD
  175186. 11708
  175187. 12717N
  175188. 2/28/96V
  175189. ILLUMINATI, G.; MANDOLINI, L. RING CLOSURE REACTIONS OF BIFUNCTIONAL CHAIN MOLECULES. 1981,14, 95. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175190. GABRIEL WEATHERHEAD
  175191. 11709
  175192. 12718N
  175193. 2/28/96
  175194. CAINELLI, G., CARDILLO, G. SOME ASPECTS OF THE STEREOSPECIFIC SYNTHESIS OF TERPENOIDS BY MEANS OF ISOPRENE UNITS. 1981, 14, 89. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175195. GABRIEL WEATHERHEAD
  175196. 11710
  175197. 12719N
  175198. 2/28/96V
  175199. DEV, S. ASPECTS OF LONGIFOLENE CHEMISTRY. AN EXAMPLE OF ANOTHER FACET OF NATURAL PRODUCTS CHEMISTRY. 1981,14, 82. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175200. GABRIEL WEATHERHEAD
  175201. 11711
  175202. 12720N
  175203. 2/28/96V
  175204. KOBAYASHI, Y.; KUMADAKI, I. VALENCE BOND ISOMERS OF AROMATIC COMPOUNDS STABILIZED BY TRIFLUOROMETHYL GROUPS. 1981,14, 76. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175205. GABRIEL WEATHERHEAD
  175206. 11712
  175207. 12721N
  175208. 2/28/96V
  175209. BORDEN, W. T.; DAVIDSON, E. R. THEORETICAL STUDIES OF DIRADICALS CONTAINING FOUR PI ELECTRONS. 1981,14, 69. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175210. GABRIEL WEATHERHEAD
  175211. 11713
  175212. 12722N
  175213. 2/28/96
  175214. RAPPOPORT, Z. NUCLEOPHILIC VINYLIC SUBSTITUTION. A SINGLE MULTI STEP PROCESS 1981,14, 7. ACCOUNTS OF CHEMICAL RESEARCH A REVIEW.a
  175215. GABRIEL WEATHERHEAD
  175216. 11714
  175217. 12723N
  175218. 2/28/96V
  175219. REDUCTION WITH ALUMINUM ALKOXIDES (THE MEERWEIN PONNDORF VERLEY REDUCTION) A L WILDS ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  175220. GABRIEL WEATHERHEAD
  175221. 11715
  175222. 12724N
  175223. 2/28/96VyTHE FORMATION OF CYCLIC KETONES BY INTRAMOLECULAR ACYLATION WILLIAM S JOHNSON ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  175224. GABRIEL WEATHERHEAD
  175225. 11716
  175226. 12725N
  175227. 2/28/96VPTHE CANNIZZARO REACTION T A GEISSMAN ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  175228. GABRIEL WEATHERHEAD
  175229. 11717
  175230. 12726N
  175231. 2/28/96VjTHE PREPARATION OF ALIPHATIC FLUORINE COMPOUNDS ALBERT L HENNE ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  175232. GABRIEL WEATHERHEAD
  175233. 11718
  175234. 12727N
  175235. 2/28/96VWTHE CLAISEN REARRANGEMENT D STANLEY TARBELL ORGANIC REACTIONS VOLUME 2 (1944) A REVIEW.a
  175236. GABRIEL WEATHERHEAD
  175237. 11719
  175238. 12728N
  175239. 2/28/96VQTHE JACOBSEN REACTION LEE IRVIN SMITH ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175240. GABRIEL WEATHERHEAD
  175241. 11720
  175242. 12729N
  175243. 2/28/96VHTHE FRIES REACTION A H BLATT ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175244. GABRIEL WEATHERHEAD
  175245. 11721
  175246. 12730N
  175247. 2/28/96VKTHE MANNICH REACTION F F BLICKE ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175248. GABRIEL WEATHERHEAD
  175249. 11722
  175250. 12731N
  175251. 2/28/96V
  175252. THE ACETOACETIC ESTER CONDENSATION AND CERTAIN RELATED REACTIONS CHARLES R HAUSER AND BOYD E HUDSON, JR. ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175253. GABRIEL WEATHERHEAD
  175254. 11723
  175255. 12732N
  175256. 2/28/96VdTHE PERKIN REACTION AND RELATED REACTIONS JOHN R JOHNSON ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175257. GABRIEL WEATHERHEAD
  175258. 11724
  175259. 12733N
  175260. 2/28/96VTTHE CLEMMENSEN REDUCTION ELMORE L MARTIN ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175261. GABRIEL WEATHERHEAD
  175262. 11725
  175263. 12734N
  175264. 2/28/96
  175265. BVLTHE ELBS REACTION LOUIS F FIESER ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175266. GABRIEL WEATHERHEAD
  175267. 11726
  175268. 12735N
  175269. 2/28/96VPTHE BUCHERER REACTION NATHAN L DRAKE ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175270. GABRIEL WEATHERHEAD
  175271. 11727
  175272. 12736N
  175273. 2/28/96V9ARLIN T LEMER ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175274. GABRIEL WEATHERHEAD
  175275. 11728
  175276. 12737N
  175277. 2/28/96V>THE AMINATION OF HETEROCYCLIC BASES BY ALKALI AMIDES A REVIEW.a
  175278. GABRIEL WEATHERHEAD
  175279. 11729
  175280. 12738N
  175281. 2/28/96VtCHLOROMETHYLATION OF AROMATIC COMPOUNDS REYNOLD C FUSON AND C H MCKEEVER ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175282. GABRIEL WEATHERHEAD
  175283. 11730
  175284. 12739N
  175285. 2/28/96VbTHE ARNDT EISTERT REACTION W E BACHMANN AND W S STRUVE ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175286. GABRIEL WEATHERHEAD
  175287. 11731
  175288. 12740N
  175289. 2/28/96VTTHE REFORMATSKY REACTION RALPH L SHRINER ORGANIC REACTIONS VOLUME I (1942) A REVIEW.a
  175290. GABRIEL WEATHERHEAD
  175291. 11732
  175292. 12741N
  175293. 2/28/96VXJ.K.A. CLARKE, CHEM. REV., 75, 291 (1975)  SELECTIVITY IN CATALYSIS BY ALLOYS  A REVIEW.a
  175294. GABRIEL WEATHERHEAD
  175295. 11733
  175296. 12742N
  175297. 2/28/96VbK . J . KLABUNDE, ACCOUNTS CHEM . RES ., 8, 393 (1975) ORGANIC CHEMISTRY OF METAL VAPORS A REVIEW.a
  175298. GABRIEL WEATHERHEAD
  175299. 11734
  175300. 12743N
  175301. 2/28/96V
  175302. L . S . HEGEDUS, J . ORGANOMETAL . CHEM., 03, 421 (1975) . TRANSITION METALS IN ORGANIC SYNTHESIS; ANNUAL SURVEY COVERING THE YEAR 1974 A REVIEW.a
  175303. GABRIEL WEATHERHEAD
  175304. 11735
  175305. 12744N
  175306. 2/28/96V
  175307. A. H. DAVIDSON, P.K.G. HODGSON, D. HOWELLS, AND S. WARREN, CHEM. AND IND., 455 (1975). SI, P, S: ELEMENTS FOR ORGANIC SYNTHESIS   PART II A REVIEW.a
  175308. GABRIEL WEATHERHEAD
  175309. 11736
  175310. 12745N
  175311. 2/28/96VdIAN FLEMING, CHEM. AND IND., 449 (1975). SI, P, S: ELEMENTS FOR ORGANIC SYNTHESIS   PART I A REVIEW.a
  175312. GABRIEL WEATHERHEAD
  175313. 11737
  175314. 12746N
  175315. 2/28/96
  175316. L. E. GUSEL'NIKOV, N. S. NAMETKIN, V. M. VDORIN, RUSS. CHEM. REV. 43, 620 (1974). UNSTABLE SILICON ANALOGUES OF QLEFINS AND KETONES A REVIEW.a
  175317. GABRIEL WEATHERHEAD
  175318. 11738
  175319. 12747N
  175320. 2/28/96V}D. PAQUER, BULL. SOC. CHIM, FRANCE, 1439 (1975). REACTIONS OF ORGANOMAGNESIUM COMPOUNDS WITH THIOCARBONYL COMPOUNDS A REVIEW.a
  175321. GABRIEL WEATHERHEAD
  175322. 11739
  175323. 12748N
  175324. 2/28/96V
  175325. D. IVANOV, G. VASSILEV, AND I. PANAYOTOV, SYNTHESIS, 83 (1975). SYNTHESES AND REACTIONS OF ORGANOLITHIUM REAGENTS DERIVED FROM WEAKLY ACIDIC C H COMPOUNDS A REVIEW.a
  175326. GABRIEL WEATHERHEAD
  175327. 11740
  175328. 12749N
  175329. 2/28/96VYH. C. BROWN, J. ORGANOMETAL. CHEM., 100, 3 (1975) FOOTSTEPS ON THE BORANE TRAIL A REVIEW.a
  175330. GABRIEL WEATHERHEAD
  175331. 11741
  175332. 12750N
  175333. 2/28/96VpK. SMITH, CHEM. SOC. REV., 3, 443 (1974). PREPARATION OF ORGANOBORANES: REAGENTS FOR ORGANIC SYNTHESIS A REVIEW.a
  175334. GABRIEL WEATHERHEAD
  175335. 11742
  175336. 12751N
  175337. 2/28/96
  175338. E. C. ASHBY AND J. T. LAEMMLE, CHEM. REV., 75, 52L (1975). STEREOCHEMISTRY OF ORGANOMETALLIC COMPOUND ADDITION TO KETONES A REVIEW.a
  175339. GABRIEL WEATHERHEAD
  175340. 11743
  175341. 12752N
  175342. 2/28/96VlR. KEESE, ANGEW. CHEM. INT..ED., 14, 528 (1975). METHODS FOR THE PREPARATION OF BRIDGEHEAD OLEFINS A REVIEW.a
  175343. GABRIEL WEATHERHEAD
  175344. 11744
  175345. 12753N
  175346. 2/28/96V
  175347. N. KORNBLUM, ANGEW. CHEM. INT. ED., 14, 734 (1975). SUBSTITUTION REACTIONS WHICH PROCEED VIA RADICAL ANION INTERMEDIATES A REVIEW.a
  175348. GABRIEL WEATHERHEAD
  175349. 11745
  175350. 12754N
  175351. 2/28/96V
  175352. R. VALTERS, RUSS. CHEM. REV., 43, 665 (1974) RING CHAIN ISOMERIC TRANSFORMATIONS OF HYDROXY , AMINO , AND MERCAPTO DERIVATIVES OF CARBONYL COMPOUNDS AND THEIR HETEROANALOGUES A REVIEW.a
  175353. GABRIEL WEATHERHEAD
  175354. 11746
  175355. 12755N
  175356. 2/28/96VpJ. CORNELISSE AND E. HAVINGA, CHEM. REV., 353 (1975) PHOTOSUBSTITUTION REACTIONS OF AROMATIC COMPOUNDS A REVIEW.a
  175357. GABRIEL WEATHERHEAD
  175358. 11747
  175359. 12756N
  175360. 2/28/96
  175361. XViY. MAZUR, PURE AND APPL. CHEM., 41, 145 (1975). FUNCTIONALIZATION OF NON ACTIVATED CARBON ATOMS A REVIEW.a
  175362. GABRIEL WEATHERHEAD
  175363. 11748
  175364. 12757N
  175365. 2/28/96VPF. I. LUKNITSKII, CHEM. REV., 75, 259 (1975)  THE CHEMISTRY OF CHLORAL A REVIEW.a
  175366. GABRIEL WEATHERHEAD
  175367. 11749
  175368. 12758N
  175369. 2/28/96V[M. REGITZ, ANGEW. CHEM. INT. ED., 14, 222, (1975) CHEMISTRY OF PHOSPHORYLCARBENES A REVIEW.a
  175370. GABRIEL WEATHERHEAD
  175371. 11750
  175372. 12759N
  175373. 2/28/96VTG. L'ABBE, ANGEW. CHEM. INT. ED., 14, 775 (1975) REACTIONS OF VINYL AZIDES A REVIEW.a
  175374. GABRIEL WEATHERHEAD
  175375. 11751
  175376. 12760N
  175377. 2/28/96VqA. L. RUSANOV, RUSS. CHEM. REV., 43, 795 (1974) THE CHEMISTRY OF UNSUBSTITUTED MONO  AND DI AMIDRAZONES A REVIEW.a
  175378. GABRIEL WEATHERHEAD
  175379. 11752
  175380. 12761N
  175381. 2/28/96VzL. A. YANOVSKAYA AND V. A. DOMBROVSKII, RUSS. CHEM. REV., 44, 154 (1975). FUNCTIONALLY SUBSTITUTED CYCLOPROPANES A REVIEW.a
  175382. GABRIEL WEATHERHEAD
  175383. 11753
  175384. 12762N
  175385. 2/28/96
  175386. N. P. BEDNYAGINA, I. YA. POSTOVSKII, A. D. GARNOVSKII, AND O. A. OSIPOV, RUSS. CHEM. REV., 44, 493 (1975) HETARYLFORMAZANS A REVIEW.a
  175387. GABRIEL WEATHERHEAD
  175388. 11754
  175389. 12763N
  175390. 2/28/96VeL. A. PAQUETTE, TETRAHEDRON, 31, 2855 (1975) THE RENAISSANCE IN CYCLOOCTATETRAENE CHEMISTRY A REVIEW.a
  175391. GABRIEL WEATHERHEAD
  175392. 11755
  175393. 12764N
  175394. 2/28/96VlW. FLITSCH AND S. R. SCHINDLER, SYNTHESIS, 685 (1975). ALKENYLATION OF IMIDES AND ACTIVATED AMIDES A REVIEW.a
  175395. GABRIEL WEATHERHEAD
  175396. 11756
  175397. 12765N
  175398. 2/28/96V~R. ESMAIL AND F. KURZER, SYNTHESIS, 301 (1975)  THE CHEMISTRY OF ETHOXYCARBONYL ISOTHIOCYANATE AND RELATED COMPOUNDS A REVIEW.a
  175399. GABRIEL WEATHERHEAD
  175400. 11757
  175401. 12766N
  175402. 2/28/96V
  175403. D.ST.C. BLACK, R. F. CROZIER, AND V. C. DAVIS, SYNTHESIS, 205 (1975). 1,3 DIPOLAR CYCLOADDITION REACTIONS OF NITRONES A REVIEW.a
  175404. GABRIEL WEATHERHEAD
  175405. 11758
  175406. 12767N
  175407. 2/28/96
  175408. R. APPEL, ANGEW. CHEM. INT. ED., 14, 801 (1975) . TERTIARY PHOSPHINE/TETRACHLOROMETHANE, A VERSATILE REAGENT FOR CHLORINATION, DEHYDRATION, AND P N LINKAGE'' A REVIEW.a
  175409. GABRIEL WEATHERHEAD
  175410. 11759
  175411. 12768N
  175412. 2/28/96V[A. W. JOHNSON. CHEM. SOC. REV., 4, 1 (1975 )  PORPHYRINS AND RELATED RING SYSTEMS A REVIEW.a
  175413. GABRIEL WEATHERHEAD
  175414. 11760
  175415. 12769N
  175416. 2/28/96V
  175417. W. DURCKHEIMER, ANQEW. CHEM. INT. ED., 4, 721 (1975). TETRACYCLINES: CHEMISTRY, BIOCHEMISTRY, AND STRUCTURE ACTIVITY RELATIONS A REVIEW.a
  175418. GABRIEL WEATHERHEAD
  175419. 11761
  175420. 12770N
  175421. 2/28/96V
  175422. S. E. ZURABYAN AND A. Y. KHORLIN, RUSS. CHEM. REV., 43, 887 (1974). ADVANCES IN THE SYNTHETIC CHEMISTRY OF AMINOGLYCOSIDES A REVIEW.a
  175423. GABRIEL WEATHERHEAD
  175424. 11762
  175425. 12771N
  175426. 2/28/96VyS. M. WEINREB AND M. F. SEMMELHACK, ACCOUNTS CHEM. RES., 8, 158 (1975). SYNTHESIS OF THE CEPHALOTAXUS ALKALOIDS A REVIEW.a
  175427. GABRIEL WEATHERHEAD
  175428. 11763
  175429. 12772N
  175430. 2/28/96
  175431. hVpD. ARIGONI, PURE AND APPL. CHEM., 41, 219 (1975). STEREOCHEMICAL ASPECTS OF SESQUITERPENE BIOSYNTHESIS A REVIEW.a
  175432. GABRIEL WEATHERHEAD
  175433. 11764
  175434. 12773N
  175435. 2/28/96VwE. E. VAN TAMELEN, ACCOUNTS CHEM. RES., 8, 152 (1975). TOTAL SYNTHESIS OF TETRA AND PENTACYCLIC TRITERPENOIDS A REVIEW.a
  175436. GABRIEL WEATHERHEAD
  175437. 11765
  175438. 12774N
  175439. 2/28/96VtC. DJERASSI, PURE AND APPL. CHEM., 41, 113 (1975). NATURAL PRODUCTS CHEMISTRY 1950 1980    A PERSONAL VIEW A REVIEW.a
  175440. GABRIEL WEATHERHEAD
  175441. 11766
  175442. 12775N
  175443. 2/28/96VdR. N. BUTLER, CHEM. REV., 75, 241 (1975). THE DIAZOTIZATION OF HETEROCYCLIC PRIMARY AMINES A REVIEW.a
  175444. GABRIEL WEATHERHEAD
  175445. 11767
  175446. 12776N
  175447. 2/28/96VmN. P. SHUSHERINA, RUSS. CHEM. REV., 43, 851 (1974) . DIENE SYNTHESIS WITH 2 PYRONES AND 2 PYRIDONES A REVIEW.a
  175448. GABRIEL WEATHERHEAD
  175449. 11768
  175450. 12777N
  175451. 2/28/96VWM. B. RUBIN, CHEM. REV., 75, 177 (1975). THE CHEMISTRY OF VICINAL POLYKETONES A REVIEW.a
  175452. GABRIEL WEATHERHEAD
  175453. 11769
  175454. 12778N
  175455. 2/28/96V
  175456. G. DESIMONI AND G. TACCONI, CHEM. REV., 75, 651 (1975). HETERODIENE SYNTHESES WITH ALPHA, BETA UNSATURATED CARBONYL COMPOUNDS A REVIEW.a
  175457. GABRIEL WEATHERHEAD
  175458. 11770
  175459. 12779N
  175460. 2/28/96V
  175461. C. REICHARDT AND K. HALBRITTER, ANGEW. CHEM. INT. ED., 14, 86 (1975). PREPARATION, STRUCTURE, AND REACTIONS OF HALOMALONDIALDEHYDES A REVIEW.a
  175462. GABRIEL WEATHERHEAD
  175463. 11771
  175464. 12780N
  175465. 2/28/96VxJ. M. CONIA AND P. LE PERCHEC, SYNTHESIS, 1, (1975). THE THERMAL CYCLISATION OF UNSATURATED CARBONYL COMPOUNDS A REVIEW.a
  175466. GABRIEL WEATHERHEAD
  175467. 11772
  175468. 12781N
  175469. 2/28/96V]P. D. KENNEWELL AND J. B. TAYLOR, CHEM. SOC. REV., 4, 189 (1975). THE SULPHOXIMIDES A REVIEW.a
  175470. GABRIEL WEATHERHEAD
  175471. 11773
  175472. 12782N
  175473. 2/28/96VcM. D. COHEN, ANGEW. CHEM. INT. ED., 14, 386 (1975) . THE PHOTOCHEMISTRY OF ORGANIC SOLIDS A REVIEW.a
  175474. GABRIEL WEATHERHEAD
  175475. 11774
  175476. 12783N
  175477. 2/28/96
  175478. V. M. GRYAZNOV AND V. S. SMIRNOV, RUSS. CHEM. REV., 43, 821 (1974). THE REACTIONS OF HYDROCARBONS ON MEMBRANE CATALYSTS A REVIEW.a
  175479. GABRIEL WEATHERHEAD
  175480. 11775
  175481. 12784N
  175482. 2/28/96VPA. I. KESTNER, RUSS. CHEM. REV., 43, 690 (1974 ) . IMMOBILIZED ENZYMES A REVIEW.a
  175483. GABRIEL WEATHERHEAD
  175484. 11776
  175485. 12785N
  175486. 2/28/96VIB.J.F. HUDSON, CHEM. AND IND., 1059 (1975). IMMOBILIZED ENZYMES A REVIEW.a
  175487. GABRIEL WEATHERHEAD
  175488. 11777
  175489. 12786N
  175490. 2/28/96VgC. J. SUCKLING AND K. E. SUCKLING, CHEM. SOC . REV., 3, (1974) . ENZYMES IN ORGANIC SYNTHESIS A REVIEW.a
  175491. GABRIEL WEATHERHEAD
  175492. 11778
  175493. 12787N
  175494. 2/28/96VnT. H. LO. CHEM. REV., 75, 1 (1975). THE HARD SOFT ACIDS BASES (HSAB) PRINCIPLE AND ORGANIC CHEMISTRY A REVIEW.a
  175495. GABRIEL WEATHERHEAD
  175496. 11779
  175497. 12788N
  175498. 2/28/96V[S. TURNER, CHEM. AND IND., 445 (1975). PRINCIPLES OF SYNTHETIC DESIGN IN PRACTICE A REVIEW.a
  175499. GABRIEL WEATHERHEAD
  175500. 11780
  175501. 12789N
  175502. 2/28/96
  175503. yVnK. B. RALL', A. I. VIL'DAVSKAYA, AND A. A. PETROV, RUSS. CHEM. REV., 44, 373 (1975). NITROACETYLENES A REVIEW.a
  175504. GABRIEL WEATHERHEAD
  175505. 11781
  175506. 12790N
  175507. 2/28/96VFE. V. BROWN, SYNTHESIS, 358, (1975). THE WILLGERODT REACTION A REVIEW.a
  175508. GABRIEL WEATHERHEAD
  175509. 11782
  175510. 12791N
  175511. 2/28/96V
  175512. I. L. KNUYNANTS AND V. R. POLISHCHUK, RUSS. CHEM. REV., 44, 339 (1975). ADVANCES IN THE SYNTHESIS AND INVESTIGATION OF ORGANOFLUORINE COMPOUNDS A REVIEW.a
  175513. GABRIEL WEATHERHEAD
  175514. 11783
  175515. 12792N
  175516. 2/28/96V]K. LEY AND F. SENG, SYNTHESIS, 415 (1975) . SYNTHETIC APPLICATIONS OF BENZOFUROXANS A REVIEW.a
  175517. GABRIEL WEATHERHEAD
  175518. 11784
  175519. 12793N
  175520. 2/28/96V
  175521. R. R. SCHMIDT, ANGEW. CHEM. INT. ED., 14, 581 (1975). HETEROCYCLIC SYSTEMS HAVING EIGHT PI ELECTRONS. SYNTHESIS, PROPERTIES, AND SIGNIFICANCE A REVIEW.a
  175522. GABRIEL WEATHERHEAD
  175523. 11785
  175524. 12794N
  175525. 2/28/96
  175526. ~VzD. J. ANDERSON AND A. HASSNER, SYNTHESIS, 483 (1975). SYNTHESIS OF HETEROCYCLES VIA CYCLOADDITIONS TO L AZIRINES A REVIEW.a
  175527. GABRIEL WEATHERHEAD
  175528. 11786
  175529. 12795N
  175530. 2/28/96VyL. J. MATHIAS AND C. G. OVERBERGER, SYNTH. COMM., 5 , 461 (1975) . SYNTHESES OF FORMAMIDINES AND BENZIMIDAZOLES A REVIEW.a
  175531. GABRIEL WEATHERHEAD
  175532. 11787
  175533. 12796N
  175534. 2/28/96V
  175535. T. NISHIWAKI, SYNTHESIS, 20 (1975). SYNTHESIS OF HETEROCYCLES BY MEANS OF THE RING TRANSFORMATION REACTIONS OF MONOCYCLIC AND CONDENSED 1,2 0XAZOLES (ISOXAZOLES) A REVIEW.a
  175536. GABRIEL WEATHERHEAD
  175537. 11788
  175538. 12797N
  175539. 2/28/96V
  175540. A. V. FOLKIN AND A. F. KOLOMIETS, RUSS. CHEM. REV., 44, 138 (1975). THE STRUCTURE AND METHODS OF SYNTHESIS OF THIIRANES A REVIEW.a
  175541. GABRIEL WEATHERHEAD
  175542. 11789
  175543. 12798N
  175544. 2/28/96VyV. AMARNATH AND R. MADHAV, SYNTHESIS, 837 (1974). A SURVEY OF METHODS FOR THE PREPARATION OF PYRROLOPYRIMIDINES A REVIEW.a
  175545. GABRIEL WEATHERHEAD
  175546. 11790
  175547. 12799N
  175548. 2/28/96
  175549. R. B. GAMMILL, C. A. WILSON, AND T. A. BRYSON, SYNTH. COMM., 5, 245 (1975). SYNTHESIS OF ALPHA METHYLENE GAMMA BUTYROLACTONES A REVIEW.a
  175550. GABRIEL WEATHERHEAD
  175551. 11791
  175552. 12800N
  175553. 2/28/96VcP. A. GRIECO, SYNTHESIS, 67 (1975). METHODS FOR THE SYNTHESIS OF ALPHA METHYLENE LACTONES A REVIEW.a
  175554. GABRIEL WEATHERHEAD
  175555. 11792
  175556. 12801N
  175557. 2/28/96VpA. K. MUKERJEE AND A. K. SINGH, SYNTHESIS, 547 (1975). REACTIONS OF NATURAL AND SYNTHETIC BETA LACTAMS A REVIEW.a
  175558. GABRIEL WEATHERHEAD
  175559. 11793
  175560. 12802N
  175561. 2/28/96V
  175562. E. WINTERFELDT, SYNTHESIS, 617 (1975). APPLICATIONS OF DIISOBUTYLALUMINUM HYDRIDE (DIBAH) AND TRIISOBUTYLALUMINUM (TIBA) AS REDUCING AGENTS IN ORGANIC SYNTHESIS A REVIEW.a
  175563. GABRIEL WEATHERHEAD
  175564. 11794
  175565. 12803N
  175566. 2/28/96V
  175567. C. F. LANE, SYNTHESIS, 135 (1975). SODIUM CYANOBOROHYDRIDE   A HIGHLY SELECTIVE REDUCING AGENT OF ORGANIC FUNCTIONAL GROUPS A REVIEW.a
  175568. GABRIEL WEATHERHEAD
  175569. 11795
  175570. 12804N
  175571. 2/28/96
  175572. L. S. HEGEDUS, J. ORGANOMETAL. CHEM., 103, 421 TRANSITION METALS IN ORGANIC SYNTHESIS; ANNUAL SURVEY COVERING THE YEAR 1974. A REVIEW.a
  175573. GABRIEL WEATHERHEAD
  175574. 11796
  175575. 12805N
  175576. 2/28/96VkR. J. HAINES AND G. J. LEIGH, CHEM. SOC. REV. 4, 155 (1975). OLEFIN METATHESIS AND ITS CATALYSIS. A REVIEW.a
  175577. GABRIEL WEATHERHEAD
  175578. 11797
  175579. 12806N
  175580. 2/28/96V
  175581. L. A. PAQUETTE, SYNTHESIS, 1975, 347. PREPARATIVE ASPECTS OF SILVER ION CATALYZED REARRANGEMENTS OF POLYCYCLIC SYSTEMS. A REVIEW.a
  175582. GABRIEL WEATHERHEAD
  175583. 11798
  175584. 12807N
  175585. 2/28/96VuT. SAEGUSA AND Y. ITO, SYNTHESIS, 1975, 291. SYNTHESIS OF CYCLIC COMPOUNDS VIA COPPER ISONITRILE COMPLEXES. A REVIEW.a
  175586. GABRIEL WEATHERHEAD
  175587. 11799
  175588. 12808N
  175589. 2/28/96V
  175590. J. P. COLLMAN, ACC. CHEM. RES., 8, 342 (1975). DISODIUM TETRACARBONYLFERRATE   A TRANSITION METAL ANALOG OF A GRIGNARD REAGENT. A REVIEW.a
  175591. GABRIEL WEATHERHEAD
  175592. 11800
  175593. 12809N
  175594. 2/28/96
  175595. H. FELKIN AND G. SWIERCZEWSKI, TETRAHEDRON, 31, 2735 (1975 ) . ACTIVATION OF GRIGNARD REAGENTS BY TRANSITION METAL COMPOUNDS. A REVIEW.a
  175596. GABRIEL WEATHERHEAD
  175597. 11801
  175598. 12810N
  175599. 2/28/96V
  175600. D . S . MATTESON , SYNTHESIS, 1975, 147 . METHANETETRABORONIC AND METHANETRIBORONIC ESTERS AS SYNTHETIC INTERMEDIATES. A REVIEW.a
  175601. GABRIEL WEATHERHEAD
  175602. 11802
  175603. 12811N
  175604. 2/28/96VvJ. CORNELISSE AND E. HAVINGA, CHEM. REV., 75, 353 (1975). PHOTOSUBSTITUTION REACTIONS OF AROMATIC COMPOUNDS. A REVIEW.a
  175605. GABRIEL WEATHERHEAD
  175606. 11803
  175607. 12812N
  175608. 2/28/96V
  175609. R. MIETHCHEN AND C. F. KROGER, Z. CHEM., 15, 135 (1975) THE REACTION OF AROMATICS WITH ALKANES AND CYCLOALKANES IN THE PRESENCE OF FRIEDEL CRAFTS CATALYSTS. A REVIEW.a
  175610. GABRIEL WEATHERHEAD
  175611. 11804
  175612. 12813N
  175613. 2/28/96V
  175614. G. DESIMONI AND G. TACCONI, CHEM. REV., 75, 651 (1975). HETERODIENE SYNTHESIS WITH ALPHA, BETA UNSATURATED CARBONYL COMPOUNDS. ONLY THERMAL CYCLOADDITIONS ARE COVERED. A REVIEW.
  175615. GABRIEL WEATHERHEAD
  175616. 11805
  175617. 12814N
  175618. 2/28/96VvJ. M. CONIA AND P. LEPERCHEC, SYNTHESIS, 1975, 1. THE THERMAL CYCLISATION OF UNSATURATED CARBONYL COMPOUNDS. A REVIEW.a
  175619. GABRIEL WEATHERHEAD
  175620. 11806
  175621. 12815N
  175622. 2/28/96V
  175623. L. A. YANOVSKAYA AND Y. A. DOMBROVSKII, RUSS. CHEM. REV., 44, 154 (1975). FUNCTIONALLY SUBSTITUTED CYCLOPROPANES. INCLUDES A SECTION ON THE SYNTHESIS OF THESE COMPOUNDS. A REVIEW.a
  175624. GABRIEL WEATHERHEAD
  175625. 11807
  175626. 12816N
  175627. 2/28/96V}K.P.C.VOLLHARDT, SYNTHESIS, 1975, 765. BIS WITTIG REACTIONS IN THE SYNTHESIS OF NONBENZENOID AROMATIC RING SYSTEMS. A REVIEW.a
  175628. GABRIEL WEATHERHEAD
  175629. 11808
  175630. 12817N
  175631. 2/28/96V
  175632. K. M. MINACHEV, Y. S. KHODAKOV, AND V. S. NAKHSHUNOV, RUSS. CHEM. REV., 45, 142 (1976). HYDROGENATION OF ALKENES ON OXIDE CATALYSTS A REVIEW.a
  175633. GABRIEL WEATHERHEAD
  175634. 11809
  175635. 12818N
  175636. 2/28/96
  175637. VvR. N. BUTLER, CHEM. AND IND., 499 (1976). LEAD TETRAACETATE ACETOXYLATION OF THE HETEROALLYLIC SYSTEM C=X YH A REVIEW.a
  175638. GABRIEL WEATHERHEAD
  175639. 11810
  175640. 12819N
  175641. 2/28/96VkA. J. FATIADI, SYNTHESIS, 65, 133 (1976). ACTIVE MANGANESE DIOXIDE OXIDATION IN ORGANIC CHEMISTRY A REVIEW.a
  175642. GABRIEL WEATHERHEAD
  175643. 11811
  175644. 12820N
  175645. 2/28/96VnA. H. HAINES, CHEM. AND IND., 883 (1976). SOME RECENT DEVELOPMENTS IN OXIDATION IN ORGANIC CHEMISTRY A REVIEW.a
  175646. GABRIEL WEATHERHEAD
  175647. 11812
  175648. 12821N
  175649. 2/28/96VqS. A. MASLOV AND E. A. BLYUMBERG, RUSS. CHEM. REV., 45, 155 (1976). LIQUID PHASE OXIDATION OF ALDEHYDES A REVIEW.a
  175650. GABRIEL WEATHERHEAD
  175651. 11813
  175652. 12822N
  175653. 2/28/96VqF. MINISCI, FORTSCHR. CHEM. FORSCH., 62, 1 (1976). RECENT ADVANCES OF HOMOLYTIC AROMATIC SUBSTITUTIONS. A REVIEW.a
  175654. GABRIEL WEATHERHEAD
  175655. 11814
  175656. 12823N
  175657. 2/28/96
  175658. E. HAVINGA AND J. CORNELISSE, PURE AND APPL. CHEM., 47, 1 (1976). PLENARY LECTURE: AROMATIC PHOTOSUBSTITUTION REACTIONS. A REVIEW.a
  175659. GABRIEL WEATHERHEAD
  175660. 11815
  175661. 12824N
  175662. 2/28/96V
  175663. R. HUISGEN, R. SCHUG, AND G. STEINER, BULL. SOC. CHIM. FR., 1976, 1813. CYCLOADDITIONS 2 + 2 PAR DES INTERMEDIAIRES DIPOLAIRES 1,4. A REVIEW.a
  175664. GABRIEL WEATHERHEAD
  175665. 11816
  175666. 12825N
  175667. 2/28/96V
  175668. H. STETTER, ANGEW. CHEM. INT. ED. ENGL., 5, 639 (1976). CATALYZED ADDITION OF ALDEHYDES TO ACTIVATED DOUBLE BONDS 
  175669.  A NEW SYNTHETIC APPROACH . A REVIEW.a
  175670. GABRIEL WEATHERHEAD
  175671. 11817
  175672. 12826N
  175673. 2/28/96VuG. WITTIG, FORTSCHR. CHEM. FORSCH., 67, 1 (1976). OLD AND NEW IN THE FIELD OF DIRECTED ALDOL CONDENSATIONS. A REVIEW.a
  175674. GABRIEL WEATHERHEAD
  175675. 11818
  175676. 12827N
  175677. 2/28/96
  175678. G. W. H. CHEESEMAN, R. F. COOKSON, ED.), WILEY INTERSCIENCE: NEW YORK, 1979. CONDENSED IMIDAZOLES 5,5 RING SYSTEMS (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 46, P. N. PRESTON, ED.), WILEY INTERSCIENCE: NEW YORK, 1986. 7 MEMBERED HETEROCYCLIC COMPOUNDS CONTAINING OXYGEN AND SULFUR(CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 26, A. ROSOWSKY, ED.), WILEY INTERSCIENCE: NEW YORK, 1972. THIEPIN OXEPIN A REVIEW.
  175679. GABRIEL WEATHERHEAD
  175680. 11819
  175681. 12828N
  175682. 2/28/96
  175683. 4A. MCKILLOP, PURE AND APPL. CHEM., 43, 463 (1975 ) . APPLICATIONS OF THALLIUM(III)NITRATE (TTN) TO ORGANIC SYNTHESIS PYRIDAZINES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 28, R. N. CASTLE, ED.), WILEY INTERSCIENCE: NEW YORK, 1973. CONDENSED PYRAZINES (CHEMISTRY OF HETEROCYCLIC COMPOUNDS, VOL. 35, A REVIEW.
  175684. GABRIEL WEATHERHEAD
  175685. 11820
  175686. 12829N
  175687. 2/28/96V}P. J. SMITH, CHEM. AND IND., 1025 (1976). ORGANIC SYNTHESIS VIA ORGANOTIN INTERMEDIATES    SOME RECENT DEVELOPMENTS A REVIEW.
  175688. GABRIEL WEATHERHEAD
  175689. 11821
  175690. 12830N
  175691. 2/28/96V
  175692. I. P. BELETSKAYA, G. A. ARTAMKINA, AND O. A. REUTOV, RUSS. CHEM. REV., 45, 330 (1976). THE INTERACTION OF ORGANOMETALLIC DERIVATIVES WITH INORGANIC HALIDES A REVIEW.a
  175693. GABRIEL WEATHERHEAD
  175694. 11822
  175695. 12831N
  175696. 2/28/96V]T. J. MARKS, ACCOUNTS CHEM. RES., 9, 223 (1976) . ACTINIDE ORGANOMETALLIC CHEMISTRY A REVIEW.a
  175697. GABRIEL WEATHERHEAD
  175698. 11823
  175699. 12832N
  175700. 2/28/96V
  175701. P. BEAK, ACCOUNTS CHEM. RES., 9, 230 SILVER ASSISTED REACTIONS OF CHLOROFORMATES: A NEW ROUTE TO REACTIVE CARBOCATIONS A REVIEW.a
  175702. GABRIEL WEATHERHEAD
  175703. 11824
  175704. 12833N
  175705. 2/28/96V
  175706. R. D. RIEKE, FORTSCHRITTE DER CHEM. FORSCHUNG, 59, 1 (1975). USE OF ACTIVATED METALS IN ORGANIC AND ORGANOMETALLIC SYNTHESIS A REVIEW.a
  175707. GABRIEL WEATHERHEAD
  175708. 11825
  175709. 12834N
  175710. 2/28/96V
  175711. J. SCHWARTZ AND J. A. LABINGER, ANGEW. CHEM. INT. ED., 15, 333 (1976). HYDROZIRCONATION: A NEW TRANSITION METAL REAGENT FOR ORGANIC SYNTHESIS A REVIEW.
  175712. GABRIEL WEATHERHEAD
  175713. 11826
  175714. 12835N
  175715. 2/28/96VjA. P. KOZIKOWSKI AND H. F. WETTER, SYNTHESIS, 561 (1976). TRANSITION METALS IN ORGANIC SYNTHESIS A REVIEW.a
  175716. GABRIEL WEATHERHEAD
  175717. 11827
  175718. 12836N
  175719. 2/28/96V
  175720. H. G. AURICH AND W. WEISS, FORTSCHRITTE DER CHEM. FORSCHUNG, 59, 65 (1975). FORMATION AND REACTIONS OF AMINYLOXIDES (NITROXIDES) A REVIEW.a
  175721. GABRIEL WEATHERHEAD
  175722. 11828
  175723. 12837N
  175724. 2/28/96VrW. H. KUNAU, ANGEW. CHEM. INT. ED., 15, 61 (1976). CHEMISTRY AND BIOCHEMISTRY OF UNSATURATED FATTY ACIDS A REVIEW.a
  175725. GABRIEL WEATHERHEAD
  175726. 11829
  175727. 12838N
  175728. 2/28/96V[P. VOLLHARDT, FORTSCHRITTE DER CHEM. FORSCHUNG, 59, 113 (1975). CYCLOBUTADIENOIDS A REVIEW.a
  175729. GABRIEL WEATHERHEAD
  175730. 11830
  175731. 12839N
  175732. 2/28/96V{N. V. AVERINA AND N. S. ZEFIROV, RUSS. CHEM. REV., 45, 544 (1976). ADVANCES IN THE SYNTHESIS OF HETEROADAMANTANES A REVIEW.a
  175733. GABRIEL WEATHERHEAD
  175734. 11831
  175735. 12840N
  175736. 2/28/96
  175737. VmA. J. FLOYD, S. F. DYKE, AND S. E. WARD, CHEM. REV., 76, 509 (1976). THE SYNTHESIS OF PHENANTHRENES A REVIEW.a
  175738. GABRIEL WEATHERHEAD
  175739. 11832
  175740. 12841N
  175741. 2/28/96VvH. POMMER AND A. NURRENBACH, PURE AND APPL. CHEM., 43, 527 (1975). INDUSTRIAL SYNTHESIS OF TERPENE COMPOUNDS A REVIEW.a
  175742. GABRIEL WEATHERHEAD
  175743. 11833
  175744. 12842N
  175745. 2/28/96VlB.C.L. WEEDON, PURE AND APPL. CHEM., 47, 161 (1976). SYNTHESIS OF CAROTENOIDS AND RELATED POLYENES A REVIEW.a
  175746. GABRIEL WEATHERHEAD
  175747. 11834
  175748. 12843N
  175749. 2/28/96VbF. KIENZLE, PURE AND APPL. CHEM., 47, 183 (1976). THE TECHNICAL SYNTHESES OF CAROTENOIDS A REVIEW.a
  175750. GABRIEL WEATHERHEAD
  175751. 11835
  175752. 12844N
  175753. 2/28/96VmN. COHEN, ACCOUNTS CHEM. RES., 9, 412 (1976). ASYMMETRIC INDUCTION IN 19 NORSTEROID TOTAL SYNTHESIS A REVIEW.a
  175754. GABRIEL WEATHERHEAD
  175755. 11836
  175756. 12845N
  175757. 2/28/96VoI. ERNEST, ANGEW. CHEM. INT. ED., 15, 207 (1976). A SYNTHESIS OF PROSTAGLANDINS: STRATEGY AND REALITY A REVIEW.a
  175758. GABRIEL WEATHERHEAD
  175759. 11837
  175760. 12846N
  175761. 2/28/96V|F. J. MCQUILLIN, CHEM. AND IND., 941 (1976). HOMOGENEOUS CATALYSIS IN THE FUNCTIONALISATION OF ALKENES AND ALKANES A REVIEW.a
  175762. GABRIEL WEATHERHEAD
  175763. 11838
  175764. 12847N
  175765. 2/28/96VcT. WAGNER JAUREGG, SYNTHESIS, 349 (1976). REACTIONS OF AZINES AND IMINES WITH DIENOPHILES A REVIEW.a
  175766. GABRIEL WEATHERHEAD
  175767. 11839
  175768. 12848N
  175769. 2/28/96ViE. CAMPAIGNE AND S. W. SCHNELLER, SYNTHESIS, 705 (1976). CYCLIZATION OF YLIDENEMALONODINITRILES A REVIEW.a
  175770. GABRIEL WEATHERHEAD
  175771. 11840
  175772. 12849N
  175773. 2/28/96V^C. W. SPANGLER, CHEM. REV., 76, 187 (1976). THERMAL [L,J] SIGMATROPIC REARRANGEMENTS A REVIEW.a
  175774. GABRIEL WEATHERHEAD
  175775. 11841
  175776. 12850N
  175777. 2/28/96VmA. PADWA, ANGEW. CHEM. INT. ED., 15, 123 (1976). INTRAMOLECULAR 1,3 DIPOLAR CYCLOADDITION REACTIONS A REVIEW.a
  175778. GABRIEL WEATHERHEAD
  175779. 11842
  175780. 12851N
  175781. 2/28/96
  175782. VlJ. F. LIEBMAN AND A. GREENBERG, CHEM. REV., 76, 311 (1976). A SURVEY OF STRAINED ORGANIC MOLECULES A REVIEW.a
  175783. GABRIEL WEATHERHEAD
  175784. 11843
  175785. 12852N
  175786. 2/28/96VqA. P. KRAPCHO, SYNTHESIS, 425 (1976). SYNTHESIS OF CARBOCYCLIC SPIRO COMPOUNDS VIA REARRANGEMENT ROUTES A REVIEW.a
  175787. GABRIEL WEATHERHEAD
  175788. 11844
  175789. 12853N
  175790. 2/28/96V]W. S. JOHNSON, ANGEW. CHEM. INT. ED., 15, 9 (1976). BIOMIMETIC POLYENE CYCLIZATIONS A REVIEW.a
  175791. GABRIEL WEATHERHEAD
  175792. 11845
  175793. 12854N
  175794. 2/28/96V
  175795. H. STETTER, ANGEW. CHEM. INT. ED., 15, 639 (1976). CATALYZED ADDITIONS OF ALDEHYDES TO ACTIVATED DOUBLE BONDS   A NEW SYNTHETIC APPROACH A REVIEW.a
  175796. GABRIEL WEATHERHEAD
  175797. 11846
  175798. 12855N
  175799. 2/28/96V\R. E. GAWLEY, SYNTHESIS, 777 (1975). THE ROBINSON ANNELATION AND RELATED REACTIONS A REVIEW.a
  175800. GABRIEL WEATHERHEAD
  175801. 11847
  175802. 12856N
  175803. 2/28/96VrJ. D'ANGELO, TETRAHEDRON, 32, 2979 (1976). KETONE ENOLATES: REGIOSPECIFIC PREPARATION AND SYNTHETIC USES A REVIEW.
  175804. GABRIEL WEATHERHEAD
  175805. 11848
  175806. 12857N
  175807. 2/28/96V
  175808. R. A. ABRAMOVITCH AND I. SHINKAI ACCOUNTS CHEM. RES., 9, 192 (1976). AROMATIC SUBSTITUTION VIA NEW REARRANGEMENTS OF HETEROAROMATIC N OXIDES A REVIEW.a
  175809. GABRIEL WEATHERHEAD
  175810. 11849
  175811. 12858N
  175812. 2/28/96V
  175813. J. A. ZOLTEWICZ. FORTSCHRITTE DER CHEM. FORSCHUNG, 59, 33 (1975). NEW DIRECTIONS IN AROMATIC NUCLEOPHILIC SUBSTITUTION A REVIEW.a
  175814. GABRIEL WEATHERHEAD
  175815. 11850
  175816. 12859N
  175817. 2/28/96VxF. MINISCI, FORTSCHRITTE DER CHEM. FORSCHUNG, 62, 1 (1976). RECENT ASPECTS OF HOMOLYTIC AROMATIC SUBSTITUTIONS A REVIEW.a
  175818. GABRIEL WEATHERHEAD
  175819. 11851
  175820. 12860N
  175821. 2/28/96V\K. A. KORINEK, CHEM. AND IND., 931 (1976). ELECTRO ORGANIC OXIDATION AND REDUCTION A REVIEW.a
  175822. GABRIEL WEATHERHEAD
  175823. 11852
  175824. 12861N
  175825. 2/28/96V^T. MUKAIYAMA. ANGEW. CHEM. INT. ED., 15, 94 (1976). OXIDATION REDUCTION CONDENSATION A REVIEW.a
  175826. GABRIEL WEATHERHEAD
  175827. 11853
  175828. 12862N
  175829. 2/28/96
  175830. VqW. KIRMSE, ANGEW. CHEM. INT. ED., 15, 251 (1976). NITROGEN AS A LEAVING GROUP: ALIPHATIC DIAZONIUM IONS A REVIEW.a
  175831. GABRIEL WEATHERHEAD
  175832. 11854
  175833. 12863N
  175834. 2/28/96V
  175835. J. K. RASMUSSEN AND A. HASSNER, CHEM. REV., 76, 389 (1976). RECENT DEVELOPMENTS IN THE SYNTHETIC USES OF CHLOROSULFONYL ISOCYANATE A REVIEW.a
  175836. GABRIEL WEATHERHEAD
  175837. 11855
  175838. 12864N
  175839. 2/28/96V}J. J. RENARD AND H. I. BOLKER, CHEM. REV., 76, 487 (1976). THE CHEMISTRY OF CHLORINE MONOXIDE (DICHLORINE MONOXIDE) A REVIEW.a
  175840. GABRIEL WEATHERHEAD
  175841. 11856
  175842. 12865N
  175843. 2/28/96V[D. H. KIM, J. HET. CHEM., 13, 179 (1976). ACETIC ANHYDRIDE AS A SYNTHETIC REAGENT A REVIEW.a
  175844. GABRIEL WEATHERHEAD
  175845. 11857
  175846. 12866N
  175847. 2/28/96ViG. OHLOFF, PURE AND APPL. CHEM., 43, 481 (1975). SINGLET OXYGEN: A REAGENT IN ORGANIC SYNTHESIS A REVIEW.a
  175848. GABRIEL WEATHERHEAD
  175849. 11858
  175850. 12867N
  175851. 2/28/96V_H. C. BROWN, PURE AND APPL. CHEM., 47. 49 (1976). ORGANOBORANES    THE MODERN MIRACLE A REVIEW.
  175852. GABRIEL WEATHERHEAD
  175853. 11859
  175854. 12868N
  175855. 2/28/96V
  175856. A. PATCHORNIK AND M. A. KRAUS, PURE AND APPL. CHEM., 46, 183 (1976). RECENT ADVANCES IN THE USE OF POLYMERS AS CHEMICAL REAGENTS A REVIEW.a
  175857. GABRIEL WEATHERHEAD
  175858. 11860
  175859. 12869N
  175860. 2/28/96V
  175861. J. I. CROWLEY AND H. RAPOPORT, ACCOUNTS CHEM. RES., 9, 135 (1976). SOLID PHASE ORGANIC SYNTHESIS: NOVELTY OR FUNDAMENTAL CONCEPT? A REVIEW.a
  175862. GABRIEL WEATHERHEAD
  175863. 11861
  175864. 12870N
  175865. 2/28/96V|G. W. GOKEL AND H. D. DURST, SYNTHESIS, 168 (1976). PRINCIPLES AND SYNTHETIC APPLICATIONS IN CROWN ETHER CHEMISTRY A REVIEW.a
  175866. GABRIEL WEATHERHEAD
  175867. 11862
  175868. 12871N
  175869. 2/28/96V
  175870. T. KAMETANI AND K. FUKUMOTO, ACCOUNTS CHEM. RES., 9, 319 (1976). TOTAL SYNTHESIS OF NATURAL PRODUCTS BY RETERO MASS SPECTRAL SYNTHESIS A REVIEW.a
  175871. GABRIEL WEATHERHEAD
  175872. 11863
  175873. 12872N
  175874. 2/28/96V_M. BERSOHN AND A. ESACK, CHEM. REV., 76, 269 (1976) . COMPUTERS AND ORGANIC SYNTHESIS A REVIEW.a
  175875. GABRIEL WEATHERHEAD
  175876. 11864
  175877. 12873N
  175878. 2/28/96V
  175879. J. B. HENDRICKSON, FORTACHRITTE DER CHEM. FORSCHUNG, 62, 49 (1976). A GENERAL PROTOCOL FOR SYSTEMATIC SYNTHESIS DESIGN A REVIEW.a
  175880. GABRIEL WEATHERHEAD
  175881. 11865
  175882. 12874N
  175883. 2/28/96VZJ. D. COYLE, CHEM. SOC. REV., 4, 523  PHOTOCHEMISTRY OF ORGANIC SULFUR COMPOUNDS A REVIEW.a
  175884. GABRIEL WEATHERHEAD
  175885. 11866
  175886. 12875N
  175887. 2/28/96VaS. M. MAKIN, PURE AND APPL. CHEM.. 47, 173 (1976). THE ENOL ETHER SYNTHESIS OF POLYENES A REVIEW.a
  175888. GABRIEL WEATHERHEAD
  175889. 11867
  175890. 12876N
  175891. 2/28/96V
  175892. G. RIO AND A. LECAS NAWRACKA, BULL. SOC. CHIM. FRANCE, 317 (1976). PREPARATION OF SATURATED AND UNSATURATED 1,4 DIKETONES A REVIEW.a
  175893. GABRIEL WEATHERHEAD
  175894. 11868
  175895. 12877N
  175896. 2/28/96V
  175897. C. WENTRUP, FORTSCHRITTE DER CHEM. FORSCHUNG, 62, 173 (1976). REARRANGEMENTS AND INTERCONVERSIONS OF CARBENES AND NITRENES A REVIEW.a
  175898. GABRIEL WEATHERHEAD
  175899. 11869
  175900. 12878N
  175901. 2/28/96
  175902. M. MAKOSZA, PURE AND APPL. CHEM., 43, 439 (1975) TWO PHASE REACTIONS IN THE CHEMISTRY OF CARBANIONS AND HALOCARBENES. A USEFUL TOOL IN ORGANLC SYNTHESIS. A REVIEW.a
  175903. GABRIEL WEATHERHEAD
  175904. 11870
  175905. 12879N
  175906. 2/28/96VNE. SCHMITZ, RUSS. CHEM. REV., 45, 16 (1976). ELECTROPHILIC AMINATION A REVIEW.a
  175907. GABRIEL WEATHERHEAD
  175908. 11871
  175909. 12880N
  175910. 2/28/96VzG. G. YAKOBSON AND V. M. VLASOV SYNTHESIS, 652 (1976). RECENT SYNTHETIC METHODS FOR POLYFLUOROAROMATIC COMPOUNDS A REVIEW.a
  175911. GABRIEL WEATHERHEAD
  175912. 11872
  175913. 12881N
  175914. 2/28/96V
  175915. V. E. PLATONOV AND G. G. YAKOBSON, SYNTHESIS, 374 (1976). THE APPLICATION OF THERMOLYTIC REACTIONS FOR THE SYNTHESES OF FLUORO ORGANIC COMPOUNDS A REVIEW.a
  175916. GABRIEL WEATHERHEAD
  175917. 11873
  175918. 12882N
  175919. 2/28/96VsW. D. MUNSLOW AND T. J. DELIA, J. HET. CHEM., 13, 675 (1976). SYNTHESES OF THE ISOMERIC BENZOQUINAZOLINES A REVIEW.a
  175920. GABRIEL WEATHERHEAD
  175921. 11874
  175922. 12883N
  175923. 2/28/96
  175924. M. NARITA AND C. U. PITTMAN, JR., SYNTHESIS, 489 (1976). PREPARATION OF TETRATHIAFULVALENES (TTF) AND THEIR SELENIUM ANALOGS   TETRASELENAFULVALENES (TSEF) A REVIEW.a
  175925. GABRIEL WEATHERHEAD
  175926. 11875
  175927. 12884N
  175928. 2/28/96VWV. Y. POCHINOK ET AL., RUSS. CHEM. REV., 45, 183 (1976). CONDENSED TETRAZOLES A REVIEW.a
  175929. GABRIEL WEATHERHEAD
  175930. 11876
  175931. 12885N
  175932. 2/28/96VwA. I. MEYERS AND E. D. MIHELICH, ANGEW. CHEM. INT. ED., 15, 270 (1976). THE SYNTHETIC UTILITY OF 2 OXAZOLINES A REVIEW.a
  175933. GABRIEL WEATHERHEAD
  175934. 11877
  175935. 12886N
  175936. 2/28/96V}J. M. PATTERSON, SYNTHESIS, 281 (1976). RECENT SYNTHETIC METHODS FOR PYRROLES AND PYRROLENINES (2H  OR 3H PYRROLES) A REVIEW.a
  175937. GABRIEL WEATHERHEAD
  175938. 11878
  175939. 12887N
  175940. 2/28/96VtT. UCHIDA AND K. MATSUMOTO, SYNTHESIS, 209 (1976) . METHODS FOR THE CONSTRUCTION OF THE INDOLIZINE NUCLEUS A REVIEW.a
  175941. GABRIEL WEATHERHEAD
  175942. 11879
  175943. 12888N
  175944. 2/28/96
  175945. VbF. KROHNKE. SYNTHESIS, 1 (1976). THE SPECIFIC SYNTHESIS OF PYRIDINES AND 0LIGOPYRIDINES  A REVIEW.a
  175946. GABRIEL WEATHERHEAD
  175947. 11880
  175948. 12889N
  175949. 2/28/96ViY. S. RAO, CHEM. REV., 76, 625 (1976). RECENT ADVANCES IN THE CHEMISTRY OF UNSATURATED LACTONES A REVIEW.a
  175950. GABRIEL WEATHERHEAD
  175951. 11881
  175952. 12890N
  175953. 2/28/96V
  175954. Y. KISHI, PURE AND APPL. CHEM., 43, 423 (1975) SYNTHETIC STUDIES IN THE FIELDS OF NATURAL PRODUCTS (PENICILLINS AND CEPHALOSPORINS) A REVIEW.a
  175955. GABRIEL WEATHERHEAD
  175956. 11882
  175957. 12891N
  175958. 2/28/96VcP. G. SAMMES, CHEM. REV., 76, 113 (1976). RECENT CHEMISTRY OF THE BETA LACTAM ANTIBIOTICS A REVIEW.a
  175959. GABRIEL WEATHERHEAD
  175960. 11883
  175961. 12892N
  175962. 2/28/96VXN. S. ISAACS, CHEM. SOC. REV., 5, 181 (1976). SYNTHETIC ROUTES TO BETA LACTAMS A REVIEW.a
  175963. GABRIEL WEATHERHEAD
  175964. 11884
  175965. 12893N
  175966. 2/28/96
  175967. H. B. KAGAN, PURE AND APPL. CHEM., 43, 401 (1975). ASYMMETRIC CATALYSIS BY CHIRAL RHODIUM COMPLEXES IN HYDROGENATION AND HYDROSILYLATION REACTIONS A REVIEW.a
  175968. GABRIEL WEATHERHEAD
  175969. 11885
  175970. 12894N
  175971. 2/28/96V
  175972. O. N. CHUPAKHIN AND I. YA. POSTOVSKII, RUSS. CHEM. REV., 45, 454 (1976). NUCLEOPHILIC SUBSTITUTION OF HYDROGEN IN AROMATIC SYSTEMS A REVIEW.a
  175973. GABRIEL WEATHERHEAD
  175974. 11886
  175975. 12895N
  175976. 2/28/96V{E.R.H. WALKER, CHEM. SOC. REV., 5. 23 (1976). THE FUNCTIONAL GROUP SELECTIVITY OF COMPLEX HYDRIDE REDUCING AGENTS A REVIEW.a
  175977. GABRIEL WEATHERHEAD
  175978. 11887
  175979. 12896N
  175980. 2/28/96V
  175981. D. J. RABER AND W. C. GUIDA, J. ORG. CHEM., 41, 690 (1976). USE OF BU4NBH4 AS A REDUCING AGENT. VERY SIMILAR TO NABH4, BUT MAY BE USED IN CH2C12 SOLUTION. A REVIEW.a
  175982. GABRIEL WEATHERHEAD
  175983. 11888
  175984. 12897N
  175985. 2/28/96V^C. F. LANE, CHEM. REV., 76, 773 (1976). REDUCTION OF ORGANIC COMPOUNDS WITH DIBORANE A REVIEW.a
  175986. GABRIEL WEATHERHEAD
  175987. 11889
  175988. 12898N
  175989. 2/28/96
  175990. H. C. BROWN, S. KRISHNAMURTHY, AND N. M. YOON, J. ORG. CHEM., 41, 1778 (1976). AN EXHAUSTIVE REVIEW OF THE USES OF 9 BBN AS A REDUCING AGENT IN ORGANIC CHEMISTRY. A REVIEW.a
  175991. GABRIEL WEATHERHEAD
  175992. 11890
  175993. 12899N
  175994. 2/28/96VqC. F. LANE AND G. W. KABALKA, TETRAHEDRON, 32, 981 (1976). CATECHOLBORANE. A NEW HYDROBORATION REAGENT. A REVIEW.a
  175995. GABRIEL WEATHERHEAD
  175996. 11891
  175997. 12900N
  175998. 2/28/96VbA. PELTER. CHEM. AND IND., 888 (1976). REDUCTIONS INVOLVING DIBORANE AND ITS DERIVATIVES A REVIEW.a
  175999. GABRIEL WEATHERHEAD
  176000. 11892
  176001. 12901N
  176002. 2/28/96V
  176003. I . P . BELETSKAYA , G. A. ARTAMKINA , AND 0. A. REUTOV , RUSS. CHEM. REV ., 45 , 330 (1976) . THE INTERACTION OF ORGANOMETALLIC DERIVATIVES WITH ORGANIC HALIDES. A REVIEW.a
  176004. GABRIEL WEATHERHEAD
  176005. 11893
  176006. 12902N
  176007. 2/28/96V
  176008. K. C. BISHOP, III, CHEM. REV., 76, 461 (1976) . TRANSITION METAL CATALYZED REARRANGEMENTS OF SMALL RING ORGANIC MOLECULES. A REVIEW.a
  176009. GABRIEL WEATHERHEAD
  176010. 11894
  176011. 12903
  176012. 2/28/96V
  176013. G . HENRICI  OLIVE' AND S . OLIVE' , FORTSCHR. CHEM. FORSH., 67, 107 (1976). OLEFIN INSERTION IN TRANSITION METAL CATALYSIS. A REVIEW.a
  176014. GABRIEL WEATHERHEAD
  176015. 11895
  176016. 12904N
  176017. 2/28/96VjA. P. KOZIKOWSKI AND H. F. WETTER, SYNTHESIS, 1976, 561. TRANSITION METALS IN ORGANIC SYNTHESIS. A REVIEW.a
  176018. GABRIEL WEATHERHEAD
  176019. 11896
  176020. 12905N
  176021. 2/28/96V
  176022. J. SCHWARTZ AND J. A. LABINGER, ANGEW. CHEM. INT. ED. ENGL., 15, 333 (1976). HYDROZIRCONATION: A NEW TRANSITION METAL REAGENT FOR ORGANIC SYNTHESIS. A REVIEW.a
  176023. GABRIEL WEATHERHEAD
  176024. 11897
  176025. 12906N
  176026. 2/28/96V
  176027. P. J. SMITH, CHEM. IND. (LONDON), 1976, 1025 . ORGANIC SYNTHESIS VIA ORGANIC TIN INTERMEDIATES
  176028. SOME RECENT DEVELOPMENTS. A REVIEW.a
  176029. GABRIEL WEATHERHEAD
  176030. 11898
  176031. 12907N
  176032. 2/28/96V
  176033. S. WASHBURNE, J. ORGANOMET. CHEM., 123, (1976) . SILICON APPLICATION TO ORGANIC SYNTHESIS. ANNUAL SURVEY COVERING THE YEAR 1974. A REVIEW.a
  176034. GABRIEL WEATHERHEAD
  176035. 11899
  176036. 12908N
  176037. 2/28/96
  176038. V]E. I. NEGISHI, J. ORGANOMETAL. CHEM., 108, 281 (1976) . CHEMISTRY OF ORGANOBORATES. A REVIEW.a
  176039. GABRIEL WEATHERHEAD
  176040. 11900
  176041. 12909N
  176042. 2/28/96VsB. M. MIKHAILOV, RUSS. CHEM. REV., 45 , 557 (1976) . METHODS OF SYNTHESIS AND PROPERTIES OF ALLYLBORANES. A REVIEW.a
  176043. GABRIEL WEATHERHEAD
  176044. 11901
  176045. 12910N
  176046. 2/28/96ViJ. WEILL RAYNAL, SYNTHESIS, 1976, 633. FORMATION OF CARBON CARBON BONDS BY USING ORGANOBORANES. A REVIEW.a
  176047. GABRIEL WEATHERHEAD
  176048. 11902
  176049. 12911N
  176050. 2/28/96VoC. F. LANE AND G. W. KABALKA, TETRAHEDRON, 32, 981 (1976). CATECHOLBORANE. A NEW HYDROBORATION AGENT. A REVIEW.a
  176051. GABRIEL WEATHERHEAD
  176052. 11903
  176053. 12912N
  176054. 2/28/96VnH. C. BROWN, PURE AND APPL. CHEM., 47,49 (1976 ) . PLENARY LECTURE: ORGANOBORANES
  176055. THEMODERN MIRACLE. A REVIEW.a
  176056. GABRIEL WEATHERHEAD
  176057. 11904
  176058. 12913N
  176059. 2/28/96
  176060. M. ODA, PURE APPL CHEM., 58, 7 (1986). NOVEL POLYCYCLIC CONJUGATED COMPOUNDS CONTAINING AN EIGHT MEMBERED RING: ON THE AROMATICITY OF [4N]ANNULENO [4N]ANNULENES. A REVIEW.a
  176061. GABRIEL WEATHERHEAD
  176062. 11905
  176063. 12914N
  176064. 2/28/96V
  176065. M. NEUENSCHWANDER, PURE APPL. CHEM., 58, 55 (1986). SYNTHETIC AND NMR SPECTROSCOPIC INVESTIGATION OF FULVENES AND FULVALENES. A REVIEW.a
  176066. GABRIEL WEATHERHEAD
  176067. 11906
  176068. 12915N
  176069. 2/28/96V
  176070. A. KRIEF, TETRAHEDRON, 42, 1209 (1986). SYNTHESES OF TETRAHETEROFULVALENES AND OF VINYLENE TRIHETEROCARBONATES   STRATEGY AND PRACTICE. A REVIEW.a
  176071. GABRIEL WEATHERHEAD
  176072. 11907
  176073. 12916N
  176074. 2/28/96V|H. HART, A. BASHIR HASHEMI, J. LUO AND M.A. MEADOR, TETRAHEDRON, 42, 1641 (1986). IPTYCENES, EXTENDED TRIPTYCENES. A REVIEW.a
  176075. GABRIEL WEATHERHEAD
  176076. 11908
  176077. 12917N
  176078. 2/28/96V|P.E. EATON, Y.S. OR, S.J. BRANCA AND B.K.R. SHANKAR, TETRAHEDRON, 42, 1621 (1986). THE SYNTHESIS OF PENTAPRISMANE. A REVIEW.a
  176079. GABRIEL WEATHERHEAD
  176080. 11909
  176081. 12918N
  176082. 2/28/96VoC.D. GUTSCHE AND L.G. LIN, TETRAHEDRON, 42, 1633 (1986). THE SYNTHESIS OF FUNCTIONALIZED CALIXARENES. A REVIEW.a
  176083. GABRIEL WEATHERHEAD
  176084. 11910
  176085. 12919N
  176086. 2/28/96V
  176087. H.N.C. WONG, K.L. LAU AND K.F. TAM, TOP. CURR. CHEM., 133, 83 (1986). THE APPLICATION OF CYCLOBUTANE DERIVATIVES IN ORGANIC SYNTHESIS. A REVIEW.a
  176088. GABRIEL WEATHERHEAD
  176089. 11911
  176090. 12920N
  176091. 2/28/96V
  176092. O. A. ATTANASI AND L. CAGLIOTI, ORG. PREP. PROCED. INT., 18, 299 (1986). CONJUGATED AZOALKENES: ATTRACTIVE PRODUCTS AND VERSATILE INTERMEDIATES. A REVIEW.a
  176093. GABRIEL WEATHERHEAD
  176094. 11912
  176095. 12921N
  176096. 2/28/96VkS. BRAVERMAN, CHEMISTRY OF ALLENES , WEIZMANN PRESS, JERUSALEM, 1985. BOOK: CHEMISTRY OF ALLENES. A REVIEW.a
  176097. GABRIEL WEATHERHEAD
  176098. 11913
  176099. 12922N
  176100. 2/28/96VkB. TROFIMOV, Z. CHEM., 26, 41 (1986). NEW INTERMEDIATES FOR ORGANIC SYNTHESIS BASED ON ACETYLENE. A REVIEW.a
  176101. GABRIEL WEATHERHEAD
  176102. 11914
  176103. 12923N
  176104. 2/28/96
  176105. V^P.J. GARRATT, PURE APPL. CHEM., 58, 1 (1986). SYMPOSIUM: NOVEL AROMATIC COMPOUNDS.'' A REVIEW.a
  176106. GABRIEL WEATHERHEAD
  176107. 11915
  176108. 12924N
  176109. 2/28/96VnJ.T. GUPTON, ALDRICHIMICA ACTA, 19, 43 (1986). SOME USEFUL SYNTHETIC APPLICATIONS OF GOLD'S REAGENT. A REVIEW.a
  176110. GABRIEL WEATHERHEAD
  176111. 11916
  176112. 12925N
  176113. 2/28/96VkA.J. FATIADI, SYNTHESIS, 249 (1986). NEW APPLICATIONS OF TETRACYANOETHYLENE IN ORGANIC CHEMISTRY. A REVIEW.a
  176114. GABRIEL WEATHERHEAD
  176115. 11917
  176116. 12926N
  176117. 2/28/96VHG. PIMENTEL, CHEMTECH., 16, 150 (1986). NEW REACTION PATHWAYS. A REVIEW.a
  176118. GABRIEL WEATHERHEAD
  176119. 11918
  176120. 12927N
  176121. 2/28/96VbF.E. ZIEGLER, TETRAHEDRON, 42, 2777 (1986). SYMPOSIA IN PRINT: NEW SYNTHETIC METHODS II. A REVIEW.a
  176122. GABRIEL WEATHERHEAD
  176123. 11919
  176124. 12928N
  176125. 2/28/96VgJ.B. HENDRICKSON, ACC. CHEM. RES., 19, 274 (1986). APPROACHING THE LOGIC OF SYNTHESIS DESIGN. A REVIEW.a
  176126. GABRIEL WEATHERHEAD
  176127. 11920
  176128. 12929N
  176129. 2/28/96
  176130. R.J. BERGERON, ACC. CHEM. RES., 19, 105 (1986). METHODS FOR THE SELECTIVE MODIFICATION OF SPERMIDINE AND ITS HOMOLOGUES. A REVIEW.a
  176131. GABRIEL WEATHERHEAD
  176132. 11921
  176133. 12930N
  176134. 2/28/96V
  176135. Y.F. FREIMANIS AND K. KIKOVSKAYA, CHEM. HETEROCYCL. COMPOUNDS, 22, 471 (1986). ANALOGS OF PROSTACYCLIN (PGI2) MODIFIED IN THE 2 0XABICYCLO[3.3.0]OCTANE FRAGMENT. A REVIEW.a
  176136. GABRIEL WEATHERHEAD
  176137. 11922
  176138. 12931N
  176139. 2/28/96V
  176140. R.P. EVSTIGNEEVA AND G.I. MYAGKOVA, RUSS. CHEM. REV., 55, 455 (1986). LEUKOTRIENES    NATURAL BIOLOGICALLY ACTIVE METABOLITES OF POLYUNSATURATED ACIDS. A REVIEW.a
  176141. GABRIEL WEATHERHEAD
  176142. 11923
  176143. 12932N
  176144. 2/28/96V
  176145. S.J. DANISHEFSKY, ALDRICHIMICA ACTA, 19, 59 (1986). THE EVOLUTION OF GENERAL STRATEGY FOR THE STEREOSELECTIVE CONSTRUCTION OF POLYOXYGENATED NATURAL PRODUCTS. A REVIEW.a
  176146. GABRIEL WEATHERHEAD
  176147. 11924
  176148. 12933N
  176149. 2/28/96VeK. KROHN, ANGEW. CHEM., INT. ED. ENGL., 25, 790 (1986). TOTAL SYNTHESIS OF ANTHRACYCLINONE. A REVIEW.
  176150. GABRIEL WEATHERHEAD
  176151. 11925
  176152. 12934N
  176153. 2/28/96VxC. THEBTARANONTH AND Y. THEBTARANONTH, ACC. CHEM. RES., 19, 84 (1986). NATURALLY OCCURRING CYCLOHEXENE OXIDES. A REVIEW.a
  176154. GABRIEL WEATHERHEAD
  176155. 11926
  176156. 12935N
  176157. 2/28/96V
  176158. R.R. SCHMIDT, ANGEW. CHEM., INT. ED. ENGL., 25, 212 (1986). NEW METHODS FOR THE SYNTHESIS OF GLYCOSIDES AND OLIGOSACCHARIDES   ARE THERE ALTERNATIVES TO THE KOENIGS KNORR METHOD? A REVIEW.a
  176159. GABRIEL WEATHERHEAD
  176160. 11927
  176161. 12936N
  176162. 2/28/96V^T. GNEWUCH AND G. SOSNOVSKY, CHEM. REV., 86, 203 (1986). SPIN LABELED CARBOHYDRATES. A REVIEW.a
  176163. GABRIEL WEATHERHEAD
  176164. 11928
  176165. 12937N
  176166. 2/28/96V
  176167. F.M. HAUSER AND S.R. ELLENBERGER, CHEM. REV., 86, 35 (1986). SYNTHESES OF 2,3,6 TRIDEOXY 3 AMINO AND 2,3,6 TRIDEOXY 3 NITROHEXOSES. A REVIEW.a
  176168. GABRIEL WEATHERHEAD
  176169. 11929
  176170. 12938N
  176171. 2/28/96
  176172. A.A. VAN BOECKEL, REC. TRAV. CHIM., 105, 35 (1986). SOME RECENT APPLICATIONS OF CARBOHYDRATES AND THEIR DERIVATIVES IN THE PHARMACEUTICAL INDUSTRY. A REVIEW.a
  176173. GABRIEL WEATHERHEAD
  176174. 11930
  176175. 12939N
  176176. 2/28/96VtY. THEBTARANONTH, PURE APPL. CHEM., 58, 781 (1986). SYNTHESIS AND CHEMISTRY OF CYCLOPENTENOID ANTIBIOTICS. A REVIEW.a
  176177. GABRIEL WEATHERHEAD
  176178. 11931
  176179. 12940N
  176180. 2/28/96VkC. TANN, PURE APPL. CHEM., 58, 773 (1986). STRUCTURAL STUDIES ON BIOACTIVE MICROBIAL METABOLITES. A REVIEW.a
  176181. GABRIEL WEATHERHEAD
  176182. 11932
  176183. 12941N
  176184. 2/28/96V
  176185. M. DEMUTH. PURE APPL. CHEM., 58, 1233 (1986). SYNTHESIS OF NATURAL PRODUCTS BASED ON PHOTOCHEMICAL KEY TRANSFORMATIONS. A REVIEW.a
  176186. GABRIEL WEATHERHEAD
  176187. 11933
  176188. 12942N
  176189. 2/28/96V
  176190. G. STORK AND S.D. RYCHNOVSKY, PURE APPL. CHEM., 58, 767 (1986). A GENERAL METHOD FOR THE STEREOCONTROLLED SYNTHESIS OF POLYPROPIONATE DERIVED SEQUENCES. A REVIEW.a
  176191. GABRIEL WEATHERHEAD
  176192. 11934
  176193. 12943N
  176194. 2/28/96
  176195. D.H.R. BARTON AND S.Z. ZARD, PURE APPL. CHEM., 58, 675 (1986). INVENTION OF NEW REACTIONS USEFUL IN THE CHEMISTRY OF NATURAL PRODUCTS. A REVIEW.a
  176196. GABRIEL WEATHERHEAD
  176197. 11935
  176198. 12944N
  176199. 2/28/96VdT. ROSEN AND C.H. HEATHCOCK, TETRAHEDRON, 42, 4909 (1986). THE SYNTHESIS OF MEVINIC ACIDS. A REVIEW.a
  176200. GABRIEL WEATHERHEAD
  176201. 11936
  176202. 12945N
  176203. 2/28/96V
  176204. J.D. MARTIN, J.M. PALAZON, C. PEREZ AND J.L. RAVELO, PURE APPL. CHEM., 58, 395 (1986). SYNTHESES OF MARINE MOLECULES. A REVIEW.a
  176205. GABRIEL WEATHERHEAD
  176206. 11937
  176207. 12946N
  176208. 2/28/96V
  176209. Y. WANG, PURE APPL. CHEM., 58, 653 (1986). INTERNATIONAL SYMPOSIUM ON ORGANIC CHEMISTRY OF MEDICINAL NATURAL PRODUCTS. A REVIEW.a
  176210. GABRIEL WEATHERHEAD
  176211. 11938
  176212. 12947N
  176213. 2/28/96V`M.B. GROEN AND F.J. ZEELEN, REC. TRAV. CHIM., 05, 465 (1986). STEROID TOTAL SYNTHESIS. A REVIEW.a
  176214. GABRIEL WEATHERHEAD
  176215. 11939
  176216. 12948N
  176217. 2/28/96
  176218. P.E. EATON, TETRAHEDRON, 42 1549 (1986) SYMPOSIUM IN PRINT 26: SYNTHESIS OF NON NATURAL PRODUCTS: CHALLENGE AND REWARD. A REVIEW.a
  176219. GABRIEL WEATHERHEAD
  176220. 11940
  176221. 12949N
  176222. 2/28/96VkR.E. BANKS AND J.C. TATLOW, J. FLUOR. CHEM. 33, 227 (1986). A GUIDE TO MODERN FLUORINE CHEMISTRY. A REVIEW.a
  176223. GABRIEL WEATHERHEAD
  176224. 11941
  176225. 12950N
  176226. 2/28/96V
  176227. G.A. OLAH, P.S. IYER AND G.K.S. PRAKASH, SYNTHESIS, 513 (1986). PERFLUORINATED RESINSULFONIC ACID (NAFION H) CATALYSIS IN SYNTHESIS. A REVIEW.a
  176228. GABRIEL WEATHERHEAD
  176229. 11942
  176230. 12951N
  176231. 2/28/96V
  176232. S.T. PURRINGTON, B.S. KAGEN AND T.B. PATRICK, CHEM. REV., 86, 997 (1986). THE APPLICATION OF ELEMENTAL FLUORINE IN ORGANIC SYNTHESIS. A REVIEW.a
  176233. GABRIEL WEATHERHEAD
  176234. 11943
  176235. 12952N
  176236. 2/28/96V|L. DOLBY GLOVER, CHEM. IND. (LONDON), 518 (1986). FLUOROORGANIC COMPOUNDS IN INDUSTRY: APPLICATIONS AND SYNTHESIS. A REVIEW.a
  176237. GABRIEL WEATHERHEAD
  176238. 11944
  176239. 12953N
  176240. 2/28/96
  176241. G.A. OLAH, J.G. SHIH AND G.K.S. PRAKASH, J. FLUOR. CHEM., 33, 377 (1986). FLUORINE CONTAINING REAGENTS IN ORGANIC SYNTHESIS. A REVIEW.a
  176242. GABRIEL WEATHERHEAD
  176243. 11945
  176244. 12954N
  176245. 2/28/96V
  176246. W. DMOWSKI, J. FLUOR. CHEM., 32, 255 (1986). ADVANCES IN FLUORINATION OF ORGANIC COMPOUNDS WITH SULFUR TETRAFLUORIDE. A REVIEW.a
  176247. GABRIEL WEATHERHEAD
  176248. 11946
  176249. 12955N
  176250. 2/28/96V
  176251. U.M. DZHEMILEV, O.S. VOSTRIKOVA AND A.G. IBRAGIMOV, RUSS. CHEM. REV., 55, 66 (1986). ZIRCONIUM COMPLEXES IN SYNTHESIS AND CATALYSIS. A REVIEW.a
  176252. GABRIEL WEATHERHEAD
  176253. 11947
  176254. 12956N
  176255. 2/28/96VxR.C. KERBER, J. ORGANOMETALLIC CHEM., 298, 77 (1986). ORGANOIRON CHEMISTRY. ANNUAL SURVEY FOR THE YEAR 1984 .  A REVIEW.a
  176256. GABRIEL WEATHERHEAD
  176257. 11948
  176258. 12957N
  176259. 2/28/96VsG. MARR AND B.W. ROCKETT, J. ORGANOMETALLIC. CHEM., 298, 133 ( 1986) . FERROCENE. ANNUAL SURVEY FOR 1984. A REVIEW.a
  176260. GABRIEL WEATHERHEAD
  176261. 11949
  176262. 12958N
  176263. 2/28/96
  176264. L.S. HEGEDUS, J. ORGANOMETALL. CHEM., 298, 207 ( 1986) . TRANSITION METALS IN ORGANIC SYNTHESIS. ANNUAL SURVEY FOR 1984 .  A REVIEW.a
  176265. GABRIEL WEATHERHEAD
  176266. 11950
  176267. 12959N
  176268. 2/28/96VjJ. WOLTERS AND D. DE VOS, J. ORGANOMETALL. CHEM., 313, 413 (1986). LEAD. ANNUAL SURVEY FOR 1983. A REVIEW.a
  176269. GABRIEL WEATHERHEAD
  176270. 11951
  176271. 12960N
  176272. 2/28/96V~G.0. DOAK AND L.D. FREEDMAN, J. ORGANOMETALL. CHEM., 298, 67 (1986) . BISMUTH. ANNUAL SURVEY COVERING THE YEAR 1984. A REVIEW.a
  176273. GABRIEL WEATHERHEAD
  176274. 11952
  176275. 12961N
  176276. 2/28/96VuL.D. FREEDMAN AND G.O. DOAK, J. ORGANOMETALL. CHEM., 298, 37 (1986). ANTIMONY. ANNUAL SURVEY COVERING 1984. A REVIEW.a
  176277. GABRIEL WEATHERHEAD
  176278. 11953
  176279. 12962N
  176280. 2/28/96VnN. PETRAGNANI AND J.V. COMASSETO, SYNTHESIS, 1 (1986). SYNTHETIC APPLICATIONS OF TELLURIUM REAGENTS. A REVIEW.a
  176281. GABRIEL WEATHERHEAD
  176282. 11954
  176283. 12963N
  176284. 2/28/96
  176285. S. KATO, T. MURAI AND M. ISHIDA, ORG. PREP. PROCED. INT., 18, 369 (1986). SELENIUM AND TELLURIUM ISOLOGUES OF CARBOXYLIC ACID DERIVATIVES. A REVIEW.a
  176286. GABRIEL WEATHERHEAD
  176287. 11955
  176288. 12964N
  176289. 2/28/96VzG.L. LARSON, J. ORGANOMETALL. CHEM., 313, 14 (1986). SILICON    THE SILICON CARBON BOND. ANNUAL SURVEY FOR 1984. A REVIEW.a
  176290. GABRIEL WEATHERHEAD
  176291. 11956
  176292. 12965N
  176293. 2/28/96V
  176294. J.Y. COREY, J. ORGANOMETALL. CHEM., 313, 1 (1986). SILAFUNCTIONAL COMPOUNDS: SYNTHESIS AND REACTIVITY. ANNUAL SURVEY FOR 1984. A REVIEW.a
  176295. GABRIEL WEATHERHEAD
  176296. 11957
  176297. 12966N
  176298. 2/28/96V
  176299. B. GANEM AND J.O. OSBY, CHEM. REV., 86, 763 (1986). SYNTHETICALLY USEFUL REACTIONS WITH METAL BORIDE AND ALUMINIDE CATALYSTS. A REVIEW.a
  176300. GABRIEL WEATHERHEAD
  176301. 11958
  176302. 12967N
  176303. 2/28/96VoG.W. KABALKA, ALDRICHIMICA ACTA, 19, 11 (1986). THE SYNTHESIS OF LABELED COMPOUNDS VIA ORGANOBORANES. A REVIEW.a
  176304. GABRIEL WEATHERHEAD
  176305. 11959
  176306. 12968N
  176307. 2/28/96
  176308. Y. YAMAMOTO, ANQEW. CHEM., INT. ED. ENGL., 25, 947 (1986). SELECTIVE SYNTHESIS BY USE OF LEWIS ACIDS IN THE PRESENCE OF ORGANOCOPPER AND RELATED REAGENTS. A REVIEW.a
  176309. GABRIEL WEATHERHEAD
  176310. 11960
  176311. 12969N
  176312. 2/28/96V
  176313. P. BEAK AND A.I. MEYERS, ACC. CHEM. RES., 19, 356 (1986). STEREO  AND REGIOCONTROL BY COMPLEX INDUCED PROXIMITY EFFECTS: REACTIONS OF ORGANOLITHIUM COMPOUNDS. A REVIEW.a
  176314. GABRIEL WEATHERHEAD
  176315. 11961
  176316. 12970N
  176317. 2/28/96VXR. MULLER, Z. CHEM., 193 (1986). ON THE CHEMISTRY OF ORGANOMETALLIC COMPOUNDS. A REVIEW.a
  176318. GABRIEL WEATHERHEAD
  176319. 11962
  176320. 12971N
  176321. 2/28/96V
  176322. K. SCHLOGL AND O. HOFER, PURE APPL. CHEM. 58, 481 (1986). TWELFTH INTERNATIONAL CONFERENCE ON ORGANOMETALLIC CHEMISTRY. A REVIEW.a
  176323. GABRIEL WEATHERHEAD
  176324. 11963
  176325. 12972N
  176326. 2/28/96VjM. EPHRITIKHINE, NOUV. J. CHIM., 10, 9 (1986). ACTIVATION OF ALKANE CH BONDS BY ORGANOMETALLICS. A REVIEW.a
  176327. GABRIEL WEATHERHEAD
  176328. 11964
  176329. 12973N
  176330. 2/28/96
  176331. 1VfM.P. DOYLE, CHEM. REV., 86, 919 (1986). CATALYTIC METHODS FOR METAL CARBENE TRANSFORMATIONS. A REVIEW.a
  176332. GABRIEL WEATHERHEAD
  176333. 11965
  176334. 12974N
  176335. 2/28/96V|H.D. ROTH, TETRAHEDRON, 42, 6097 (1986). SYMPOSIA IN PRINT # 28: STRUCTURE AND REACTIVITY OF ORGANIC RADICAL IONS. A REVIEW.a
  176336. GABRIEL WEATHERHEAD
  176337. 11966
  176338. 12975N
  176339. 2/28/96V]L.M. TOLBERT, ACC. CHEM. RES., 19, 268 (1986). PHOTOEXCITED STATES OF ALLYL ANIONS. A REVIEW.a
  176340. GABRIEL WEATHERHEAD
  176341. 11967
  176342. 12976N
  176343. 2/28/96VuE. VEDEJS AND F.G. WEST, CHEM. REV., 86, 941 (1986). YLIDES BY THE DESILYLATION OF ALPHA SILYL ONIUM SALTS. A REVIEW.a
  176344. GABRIEL WEATHERHEAD
  176345. 11968
  176346. 12977N
  176347. 2/28/96V[J. MANN, TETRAHEDRON, 42, 4611 (1986). THE SYNTHETIC UTILITY OF OXYALLYL CATIONS. A REVIEW.a
  176348. GABRIEL WEATHERHEAD
  176349. 11969
  176350. 12978N
  176351. 2/28/96
  176352. M. RABINOVITZ, Y. COHEN AND M. HALPERN, ANGEW. CHEM., INT. ED. ENGL., 25, 960 (1986). HYDROXIDE ION INITIATED REACTIONS UNDER PHASE TRANSFER CATALYSIS CONDITIONS:  MECHANISM AND IMPLICATIONS. A REVIEW.a
  176353. GABRIEL WEATHERHEAD
  176354. 11970
  176355. 12979N
  176356. 2/28/96VuF.D. LEWIS, ACC. CHEM. RES., I9, 401 (1986). PROTON TRANSFER REACTIONS OF PHOTOGENERATED RADICAL ION PAIRS. A REVIEW.a
  176357. GABRIEL WEATHERHEAD
  176358. 11971
  176359. 12980N
  176360. 2/28/96V
  176361. A.J.H. KLUNDER, G.J.A. ARIAANS, E.A.R.M. VAN DER LOOP AND B. ZWANENBURG, TETRAHEDRON, 42, 1903 (1986). CONTROL OF CAGE OPENING REACTIONS IN THE 1,3 BISHOMOCUBANE AND HOMOCUBANE SYSTEMS. A REVIEW.a
  176362. GABRIEL WEATHERHEAD
  176363. 11972
  176364. 12981N
  176365. 2/28/96V
  176366. R.D. LITTLE, CHEM. REV., 86, 875 (1986). THE INTRAMOLECULAR DIYL TRAPPING REACTION. A USEFUL TOOL FOR ORGANIC SYNTHESIS. A REVIEW.a
  176367. GABRIEL WEATHERHEAD
  176368. 11973
  176369. 12982N
  176370. 2/28/96
  176371. :VqG.H. POSNER, CHEM. REV., 86, 831 (1986). MULTICOMPONENT ONE POT ANNULATIONS FORMING THREE TO SIX BONDS. A REVIEW.a
  176372. GABRIEL WEATHERHEAD
  176373. 11974
  176374. 12983N
  176375. 2/28/96V
  176376. H. HIGUCHI, E. KOBAYASHI, Y. SAKATA AND S. MISUMI, TETRAHEDRON, 42, 1731 (1986). PHOTODIMERIZATION OF BENZENES IN STRAINED DIHETERA[3.3]METACYCLOPHANES. A REVIEW.a
  176377. GABRIEL WEATHERHEAD
  176378. 11975
  176379. 12984N
  176380. 2/28/96V
  176381. R.R. SCHMIDT, ACC. CHEM. RES., 19, 250 (1986). HETERO DIELS ALDER REACTION IN HIGHLY FUNCTIONALIZED NATURAL PRODUCT SYNTHESIS. A REVIEW.a
  176382. GABRIEL WEATHERHEAD
  176383. 11976
  176384. 12985N
  176385. 2/28/96VwH. PRINZBACH AND L. KNOTHE, PURE APPL. CHEM., 58, 25 (1986). MULTI ELECTRON (12PI  20PI)PERICYCLIC PROCESSES. A REVIEW.a
  176386. GABRIEL WEATHERHEAD
  176387. 11977
  176388. 12986N
  176389. 2/28/96V
  176390. B.M. TROST, ANGEW. CHEM.,INT. ED. ENQL., 25, 1 (1986). [3+2] CYCLOADDITION APPROACHES TO FIVE MEMBERED RINGS VIA TRIMETHYLENE METHANE AND ITS EQUIVALENTS. A REVIEW.a
  176391. GABRIEL WEATHERHEAD
  176392. 11978
  176393. 12987N
  176394. 2/28/96V
  176395. J. JURCZAK, S. PIKUL AND T. BAUER, TETRAHEDRON, 42, 447 (1986). (R)  AND (S) 2,3 O ISOPROPYLIDENE GLYCERALDEHYDE IN STEREOSELECTIVE ORGANIC SYNTHESIS. A REVIEW.a
  176396. GABRIEL WEATHERHEAD
  176397. 11979
  176398. 12988N
  176399. 2/28/96V|A.D. BAXTER AND S.M. ROBERTS, CHEM. IND. (LONDON), 510 (1986). ASYMMETRIC SYNTHESES OF THE PRIMARY PROSTAGLANDINS. A REVIEW.a
  176400. GABRIEL WEATHERHEAD
  176401. 11980
  176402. 12989N
  176403. 2/28/96VMD. BREMNER, CHEM. IN BRITAIN, 22, 633 (1986). CHEMICAL ULTRASONICS. A REVIEW.a
  176404. GABRIEL WEATHERHEAD
  176405. 11981
  176406. 12990N
  176407. 2/28/96VaV. RAMAMURTHY, TETRAHEDRON, 42, 5753 (1986). 0RGANIC PHOTOCHEMISTRY IN ORGANIZED MEDIA. A REVIEW.a
  176408. GABRIEL WEATHERHEAD
  176409. 11982
  176410. 12991N
  176411. 2/28/96VoR.S. DAVIDSON, PURE APPL. CHEM., 58, 1171 (1986). ELEVENTH INTERNATIONAL SYMPOSIUM ON PHOTOCHEMISTRY. A REVIEW.a
  176412. GABRIEL WEATHERHEAD
  176413. 11983
  176414. 12992N
  176415. 2/28/96
  176416. DViP. LASZLO, ACC. CHEM. RES., 19, 121 (1986). CATALYSIS OF ORGANIC REACTIONS BY INORGANIC SOLIDS. A REVIEW.a
  176417. GABRIEL WEATHERHEAD
  176418. 11984
  176419. 12993N
  176420. 2/28/96VcH. TOMINAGA, PURE APPL. CHEM., 58, 1317 (1986). SEVENTH INTERNATIONAL ZEOLITE CONFERENCE. A REVIEW.a
  176421. GABRIEL WEATHERHEAD
  176422. 11985
  176423. 12994N
  176424. 2/28/96V
  176425. J.I.G. CADOGAN, C.L. HICKSON AND H. MCNAB, TETRAHEDRON, 42, 2135 (1986) SHORT CONTACT TIME REACTIONS OF LARGE ORGANIC FREE RADICALS. A REVIEW.a
  176426. GABRIEL WEATHERHEAD
  176427. 11986
  176428. 12995N
  176429. 2/28/96VdS.G. DAVIES, CHEM. IND. (LONDON), 506 (1986). ASYMMETRIC SYNTHESIS PROSPECTS FOR INDUSTRY. A REVIEW.a
  176430. GABRIEL WEATHERHEAD
  176431. 11987
  176432. 12996N
  176433. 2/28/96VtJ.W. APSIMON AND T.L. COLLIER, TETRAHEDRON, 42, 5157 (1986). RECENT ADVANCES IN ASYMMETRIC SYNTHESIS II.'' A REVIEW.a
  176434. GABRIEL WEATHERHEAD
  176435. 11988
  176436. 12997N
  176437. 2/28/96
  176438. IVwG.B. GILL AND D.A. WHITING, ALDRICHIMICA ACTA, 9, 31 (1986). GUIDELINES FOR HANDLING AIR SENSITIVE COMPOUNDS. A REVIEW.a
  176439. GABRIEL WEATHERHEAD
  176440. 11989
  176441. 12998N
  176442. 2/28/96VQJ.B. JONES, TETRAHEDRON, 42, 3351 (1986). ENZYMES IN ORGANIC SYNTHESIS. A REVIEW.a
  176443. GABRIEL WEATHERHEAD
  176444. 11990
  176445. 12999N
  176446. 2/28/96VJP. LAVALLE, SPEC. CHEM., 6, 16 (1986). PHASE TRANSFER CATALYSIS. A REVIEW.a
  176447. GABRIEL WEATHERHEAD
  176448. 11991
  176449. 13000N
  176450. 2/28/96VuF.J.S. REED, SPEC. CHEM., 6, 3 (1986). CONTINUOUS FLOW PEPTIDE SYNTHESIS, THE ROUTE TO DRUGS OF THE FUTURE. A REVIEW.a
  176451. GABRIEL WEATHERHEAD
  176452. 11992
  176453. 13001N
  176454. 2/28/96VlN.M.M. NIBBERING, REC. TRAV. CHIM., 105, 245 (1986). GAS PHASE ORGANIC REACTIONS AT LOW PRESSURES. A REVIEW.a
  176455. GABRIEL WEATHERHEAD
  176456. 11993
  176457. 13002N
  176458. 2/28/96V
  176459. N.M. ALPATOVA, S.E. ZABUSOVA AND A.P. TOMILOV, RUSS. CHEM. REV., 55, 99 (1986). THE REDUCTION OF ORGANIC COMPOUNDS BY SOLVATED ELECTRONS GENERATED ELECTROCHEMICALLY. A REVIEW.
  176460. GABRIEL WEATHERHEAD
  176461. 11994
  176462. 13003N
  176463. 2/28/96V
  176464. E. STECKHAN, ANGEW. CHEM., INT. ED. ENGL., 25, 683 (1986). INDIRECT ELECTRO ORGANIC SYNTHESIS A MODERN CHAPTER OF ORGANIC ELECTROCHEMISTRY. A REVIEW.a
  176465. GABRIEL WEATHERHEAD
  176466. 11995
  176467. 13004N
  176468. 2/28/96VsJ. SIMONET AND G. LE GUILLANTON, BULL. SOC. CHIM.FR., 221 (1986). ELECTROCHEMICALLY INDUCED CYCLIZATIONS. A REVIEW.a
  176469. GABRIEL WEATHERHEAD
  176470. 11996
  176471. 13005N
  176472. 2/28/96V
  176473. C.K. CHU AND S.J. CUTLER, J. HETEROCYCL. CHEM., 23, 289 (1986). CHEMISTRY AND ANTIVIRAL ACTIVITIES OF ACYCLONUCLEOSIDES. A REVIEW.a
  176474. GABRIEL WEATHERHEAD
  176475. 11997
  176476. 13006N
  176477. 2/28/96VjV.M. OVRUTSKII AND L.D. PROTSENKO, RUSS. CHEM. REV., 55, 343 (1986). PHOSPHORUS ACID HYDRAZIDES. A REVIEW.a
  176478. GABRIEL WEATHERHEAD
  176479. 11998
  176480. 13007N
  176481. 2/28/96VkJ.L. MORRIS AND C.W. REES, CHEM. SOC. REV., 5, 1 (1986). 0RGANIC POLY(SULFUR NITROGEN) CHEMISTRY. A REVIEW.a
  176482. GABRIEL WEATHERHEAD
  176483. 11999
  176484. 13008N
  176485. 2/28/96
  176486. TVzJ. CHENET RAY AND R. VESSIERE, ORG. PREP. PROCED. INT., 18, 157 (1986). SYNTHESIS AND REACTIONS OF BETA SULTAMS. A REVIEW.a
  176487. GABRIEL WEATHERHEAD
  176488. 12000
  176489. 13009N
  176490. 2/28/96V
  176491. R.K. DIETER, TETRAHEDRON, 42, 3029 (1986). ALPHA OXO KETENE DITHIOACETALS AND RELATED COMPOUNDS: VERSATILE THREE CARBON SYNTHONS. A REVIEW.a
  176492. GABRIEL WEATHERHEAD
  176493. 12001
  176494. 13010N
  176495. 2/28/96VjM. MADESCLAIR, TETRAHEDRON, 42, 5459 (1986). SYNTHESIS OF SULFOXIDES BY OXIDATION OF THIOETHERS. A REVIEW.a
  176496. GABRIEL WEATHERHEAD
  176497. 12002
  176498. 13011N
  176499. 2/28/96V
  176500. P.L. FUCHS AND T.F. BRAISH, CHEM. REV., 86, 903 (1986). MULTIPLY CONVERGENT SYNTHESES VIA CONJUGATE ADDITION REACTIONS TO CYCLOALKENYL SULFONES. A REVIEW.a
  176501. GABRIEL WEATHERHEAD
  176502. 12003
  176503. 13012N
  176504. 2/28/96VRF. BECK, SPEC. CHEM., 6, 10 (1986). THIOUREA    A MULTIPURPOSE CHEMICAL. A REVIEW.a
  176505. GABRIEL WEATHERHEAD
  176506. 12004
  176507. 13013N
  176508. 2/28/96
  176509. YVtB.M. DILWORTH AND M.A.MCKERVEY, TETRAHEDRON, 42, 3731 (1986). ORGANIC SYNTHESIS WITH ALPHA CHLOROSULFIDES. A REVIEW.a
  176510. GABRIEL WEATHERHEAD
  176511. 12005
  176512. 13014N
  176513. 2/28/96V
  176514. A.G.M. BARRETT AND G.G. GRABOSKI, CHEM. REV., 86, 751 (1986). CONJUGATED NITROALKENES: VERSATILE INTERMEDIATES IN ORGANIC SYNTHESIS. A REVIEW.a
  176515. GABRIEL WEATHERHEAD
  176516. 12006
  176517. 13015N
  176518. 2/28/96V|L.B. VOLODARSKY AND A. YA. TIKHONOV, SYNTHESIS, 704 (1986). SYNTHESIS AND REACTIONS OF ALPHA HYDROXYLAMINO OXIMES. A REVIEW.a
  176519. GABRIEL WEATHERHEAD
  176520. 12007
  176521. 13016N
  176522. 2/28/96V
  176523. R. NOACK AND K. SCHWETLICH, Z. CHEM., 26, 117 (1986). CYCLOADDITIONS WITH ISOCYANATES  POTENTIALS, KINETICS, MECHANISMS. A REVIEW.a
  176524. GABRIEL WEATHERHEAD
  176525. 12008
  176526. 13017N
  176527. 2/28/96V
  176528. A.N. PUDOVIK, I.V. KONOVALOVA AND L.A. BURNAEVA, SYNTHESIS, 793 (1986). REACTIONS OF ISOCYANATO  AND SUBSTITUTED METHYLENEAMINO PHOSPHINE DERIVATIVES WITH COMPOUNDS CONTAINING MULTIPLE BONDS. A REVIEW.a
  176529. GABRIEL WEATHERHEAD
  176530. 12009
  176531. 13018N
  176532. 2/28/96V|D.N. DHAR AND K.S.K. MURTHY, SYNTHESIS, 437 (1986). RECENT ADVANCES IN THE CHEMISTRY OF CHLOROSULFONYL ISOCYANATE. A REVIEW.a
  176533. GABRIEL WEATHERHEAD
  176534. 12010
  176535. 13019N
  176536. 2/28/96VzD.L. BOGER, CHEM. REV., 86, 781 (1986). DIELS ALDER REACTIONS OF HETEROCYCLIC AZADIENES: SCOPE AND APPLICATIONS. A REVIEW.a
  176537. GABRIEL WEATHERHEAD
  176538. 12011
  176539. 13020N
  176540. 2/28/96VeH.R. SEIKALY AND T.T. TIDWELL, TETRAHEDRON, 42, 2587 (1986). ADDITION REACTIONS OF KETENES. A REVIEW.a
  176541. GABRIEL WEATHERHEAD
  176542. 12012
  176543. 13021N
  176544. 2/28/96V=R.J. CLEMENS, CHEM. REV., 86, 241 (1986). DIKETENE. A REVIEW.a
  176545. GABRIEL WEATHERHEAD
  176546. 12013
  176547. 13022N
  176548. 2/28/96V~H.C.J. OTTENHEIJM AND J.D.M. HERSCHEID, CHEM. REV., 86 697 (1986). N HYDROXY ALPHA AMINO ACIDS IN ORGANIC CHEMISTRY. A REVIEW.a
  176549. GABRIEL WEATHERHEAD
  176550. 12014
  176551. 13023N
  176552. 2/28/96
  176553. cV}G.R. NEWKOME AND G.R. BAKER, ORG. PREP. PROCED. INT., 18, 117 (1986). THE CHEMISTRY OF METHANETRICARBOXYLIC ESTERS. A REVIEW.a
  176554. GABRIEL WEATHERHEAD
  176555. 12015
  176556. 13024N
  176557. 2/28/96V
  176558. J. P. RIEN, A. BOUCHERE, H. COUSSE AND G. MOUZIN TETRAHEDRON, 42, 4095 (1986). METHODS FOR THE SYNTHESIS OF ANTIINFLAMMATORY 2 ARYLPROPIONIC ACIDS. A REVIEW.a
  176559. GABRIEL WEATHERHEAD
  176560. 12016
  176561. 13025N
  176562. 2/28/96V
  176563. H.H. WASSERMAN, K.E. MCCARTHY AND K.S. PROWSE, CHEM. REV., 86, 845 (1986). OXAZOLES IN CARBOXYLATE PROTECTION AND ACTIVATION. A REVIEW.a
  176564. GABRIEL WEATHERHEAD
  176565. 12017
  176566. 13026N
  176567. 2/28/96VUA. ALBERT, ADV. HETEROCYCL. CHEM., 40, 130 (1986). 4 AMINO 1,2,3 TRIAZOLES. A REVIEW.a
  176568. GABRIEL WEATHERHEAD
  176569. 12018
  176570. 13027N
  176571. 2/28/96VkJ. KNABE, ADV. HETEROCYCL. CHEM., 40, 105 (1986). 1,2 DIHYDROISOQUINOLINES AND RELATED COMPOUNDS. A REVIEW.a
  176572. GABRIEL WEATHERHEAD
  176573. 12019
  176574. 13028N
  176575. 2/28/96
  176576. I. HERMECZ AND L. VASUARI DEBRECZY, ADV. HETEROCYCL. CHEM., 39, 282 (1986). TRICYCLIC COMPOUNDS WITH A CENTRAL PYRIMIDINE RING AND ONE BRIDGEHEAD NITROGEN. A REVIEW.a
  176577. GABRIEL WEATHERHEAD
  176578. 12020
  176579. 13029N
  176580. 2/28/96V
  176581. T. KAMETANI AND T. HONDA, ADV. HETEROCYCL. CHEM., 39, 182 (1986). APPLICATION OF AZIRIDINES TO THE SYNTHESIS OF NATURAL PRODUCTS. A REVIEW.a
  176582. GABRIEL WEATHERHEAD
  176583. 12021
  176584. 13030N
  176585. 2/28/96VWA. LABERT, ADV. HETEROCYCL. CHEM., 39, 118 (1986). CHEMISTRY OF 8 AZAPURINES. A REVIEW.a
  176586. GABRIEL WEATHERHEAD
  176587. 12022
  176588. 13031N
  176589. 2/28/96V~J.G. KEAY, ADV. HETEROCYCL. CHEM., 39, 2 (1986)  THE REDUCTION OF NITROGEN HETEROCYCLES WITH COMPLEX METAL HYDRIDES. A REVIEW.a
  176590. GABRIEL WEATHERHEAD
  176591. 12023
  176592. 13032N
  176593. 2/28/96VuJ.C. SARMA AND R.P. SHARMA, HETEROCYCLES, 24 441 (1986). SYNTHESIS OF ALPHA METHYLENE GAMMA BUTYROLACTONES. A REVIEW.a
  176594. GABRIEL WEATHERHEAD
  176595. 12024
  176596. 13033N
  176597. 2/28/96
  176598. mVxM.J. MILLER, ACC. CHEM. RES., 19, 49 (1986). HYDROXAMATE APPROACH TO THE SYNTHESIS OF BETA LACTAM ANTIBIOTICS. A REVIEW.a
  176599. GABRIEL WEATHERHEAD
  176600. 12025
  176601. 13034N
  176602. 2/28/96V
  176603. G. MOHIUDDIN, P.S. REDDY, K. AHMED AND C.V. RATNAM, HETEROCYCLES, 24, 3489 (1986).  RECENT ADVANCES IN THE SYNTHESIS OF ANNELATED 1,4 BENZODIAZEPINES. A REVIEW.a
  176604. GABRIEL WEATHERHEAD
  176605. 12026
  176606. 13035N
  176607. 2/28/96V
  176608. G.A. MIRONOVA, V.N. KUKLIN, E.N. KIRILLOVA AND B.A. IVIN, CHEM. HETEROCYCL. COMPOUNDS, 22, 1 (1986). OXO  AND THIOXO 1,3 THIAZINES. A REVIEW.a
  176609. GABRIEL WEATHERHEAD
  176610. 12027
  176611. 13036N
  176612. 2/28/96VzW. VERBOOM AND D.N. REINHOUDT, REC. TRAV. CHIM., 05, 199 (1986). RECENT APPROACHES TO THE PYRROLO[1,2 A]INDOLES. A REVIEW.a
  176613. GABRIEL WEATHERHEAD
  176614. 12028
  176615. 13037N
  176616. 2/28/96VaM. CHRISTL, GAZZ. CHIM. ITAL., 116, 1 (1986). CYCLOADDITIONS OF 1,3,4 0XADIAZIN 6 ONES. A REVIEW.a
  176617. GABRIEL WEATHERHEAD
  176618. 12029
  176619. 13038N
  176620. 2/28/96
  176621. A.L. WEISS AND H.C. VAN DER PLAS, HETEROCYCLES, 24, 1433 (1986). DIHYDROPYRIMIDINES: SYNTHESIS, STRUCTURE AND TAUTOMERISM. A REVIEW.a
  176622. GABRIEL WEATHERHEAD
  176623. 12030
  176624. 13039N
  176625. 2/28/96V
  176626. W. STEGLICH, R. JESCHKE AND E. BUSCHMANN, GAZZ. CHIM. ITAL., 116, 361 (1986). 1,3 0XAZIN 6 ONES: VERSATILE INTERMEDIATES IN HETEROCYCLIC SYNTHESIS. A REVIEW.a
  176627. GABRIEL WEATHERHEAD
  176628. 12031
  176629. 13040N
  176630. 2/28/96VqP.G. SAMMES, GAZZ. CHIM. ITAL., 116, 109 (1986). RECENT STUDIES ON 3 0XIDOPYRYLIUM AND ITS DERIVATIVES. A REVIEW.a
  176631. GABRIEL WEATHERHEAD
  176632. 12032
  176633. 13041N
  176634. 2/28/96V
  176635. Q.B. BROXTERMAN, H. HOGEVEEN AND R.F. KINGMA, PURE AND APPL. CHEM., 58, 89 (1986). CYCLOBUTADIENE RADICAL CATIONS AND 2 AZAPYRYLIUM IONS. A REVIEW.a
  176636. GABRIEL WEATHERHEAD
  176637. 12033
  176638. 13042N
  176639. 2/28/96V
  176640. V.I. KELAREV AND G.A. SHVEKHGEIMER, CHEM. HETEROCYCL. COMPOUNDS, 22, 109 (1986). METHODS FOR THE SYNTHESIS OF AZOLES CONTAINING INDOLE SUBSTITUENTS. A REVIEW.a
  176641. GABRIEL WEATHERHEAD
  176642. 12034
  176643. 13043N
  176644. 2/28/96VsH. SUSCHITZKY, CROAT. CHEM. ACTA, 59, 57 (1986). 2H BENZIMIDAZOLES AS SYNTHONS IN HETEROCYCLIC CHEMISTRY. A REVIEW.a
  176645. GABRIEL WEATHERHEAD
  176646. 12035
  176647. 13044N
  176648. 2/28/96V~B.H. LIPSHUTZ, CHEM. REV., 86, 795 (1986). FIVE MEMBERED HETEROAROMATIC RINGS AS INTERMEDIATES IN ORGANIC SYNTHESIS. A REVIEW.a
  176649. GABRIEL WEATHERHEAD
  176650. 12036
  176651. 13045N
  176652. 2/28/96V
  176653. N. PETRAGNANI, H.M.C. FERRAZ AND G.V.J. SILVA, SYNTHESIS, 157 (1986). ADVANCES IN THE SYNTHESIS OF ALPHA METHYLENELACTONES. A REVIEW.a
  176654. GABRIEL WEATHERHEAD
  176655. 12037
  176656. 13046N
  176657. 2/28/96V
  176658. C.M. CIMARUSTI, GAZZ. CHIM. ITAL., 116, 169 (1986). MONOBACTAMS: EXPEDITIOUS SYNTHESIS OF AZETIDINONE 1 SULFONATES AND SELECTED ALTERNATIVELY ACTIVATED ANALOGS. A REVIEW.a
  176659. GABRIEL WEATHERHEAD
  176660. 12038
  176661. 13047N
  176662. 2/28/96V
  176663. YU.I. GEVAZA AND V.I. STANINETS, CHEM. HETEROCYCL. COMPOUNDS, 22, 231 (1986). ELECTROPHILIC HETEROCYCLIZATION OF UNSATURATED SULFUR AND PHOSPHORUS COMPOUNDS. A REVIEW.
  176664. GABRIEL WEATHERHEAD
  176665. 12039
  176666. 13048N
  176667. 2/28/96VaA.F. KLUGE, HETEROCYCLES, 24, 1699 (1986). SYNTHESIS OF 1,7 DIOXASPIRO [5.5] UNDECANES. A REVIEW.a
  176668. GABRIEL WEATHERHEAD
  176669. 12040
  176670. 13049N
  176671. 2/28/96VzL.S. HEGEDUS ET AL., GAZZ. CHIM. ITAL., 116, 213 (1986). PALLADIUM CATALYSIS IN THE SYNTHESIS OF INDOLOQUINONES. A REVIEW.a
  176672. GABRIEL WEATHERHEAD
  176673. 12041
  176674. 13050N
  176675. 2/28/96V
  176676. F.M. ABDEL GALIL, S.M. SHERIF AND M.H. ELNAGDI, HETEROCYCLES, 24, 2023 (1986). UTILITY OF CYANOACETAMIDE IN HETEROCYCLIC SYNTHESIS. A REVIEW.a
  176677. GABRIEL WEATHERHEAD
  176678. 12042
  176679. 13051N
  176680. 2/28/96V~R.S. VARMA AND G.W. KABALKA, HETEROCYCLES, 24, 2645 (1986). NITROALKANES IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. A REVIEW.a
  176681. GABRIEL WEATHERHEAD
  176682. 12043
  176683. 13052N
  176684. 2/28/96V
  176685. G.A. SHVEKHGEIMER, V.I. ZVOLINSKII AND K.L. KOBRAKOV, CHEM. HETEROCYCL. COMPOUNDS, 22, 353 (1986). SYNTHESIS OF HETEROCYCLES ON THE BASIS OF ALIPHATIC NITRO COMPOUNDS. A REVIEW.
  176686. GABRIEL WEATHERHEAD
  176687. 12044
  176688. 13053N
  176689. 2/28/96VxN. ONO AND A. KAJI, SYNTHESIS, 693 (1986). REDUCTIVE CLEAVAGE OF ALIPHATIC NITRO GROUPS IN ORGANIC SYNTHESIS.' A REVIEW.a
  176690. GABRIEL WEATHERHEAD
  176691. 12045
  176692. 13054N
  176693. 2/28/96VdT.S. GREENWOOD, CHEM. IND. (LONDON), 94 (1986). LOOP REACTORS FOR CATALYTIC HYDROGENATION. A REVIEW.a
  176694. GABRIEL WEATHERHEAD
  176695. 12046
  176696. 13055N
  176697. 2/28/96VrS. TORII, SYNTHESIS, 873 (1986). THE NEW ROLE OF ELECTROREDUCTIVE MEDIATORS IN ELECTROORGANIC SYNTHESIS. A REVIEW.a
  176698. GABRIEL WEATHERHEAD
  176699. 12047
  176700. 13056N
  176701. 2/28/96V
  176702. S.K. PRADHAN, TETRAHEDRON, 42, 6351 (1986). MECHANISM AND STEREOCHEMISTRY OF ALKALI METAL REDUCTIONS OF CYCLIC SATURATED AND UNSATURATED KETONES IN PROTIC SOLVENTS. A REVIEW.a
  176703. GABRIEL WEATHERHEAD
  176704. 12048
  176705. 13057N
  176706. 2/28/96V
  176707. J.D. WUEST, TETRAHEDRON, 42, 941 (1986). SYMPOSIUM IN PRINT 25: FORMAL TRANSFERS OF HYDRIDE FROM CARBON HYDROGEN BONDS. A REVIEW.a
  176708. GABRIEL WEATHERHEAD
  176709. 12049
  176710. 13058N
  176711. 2/28/96V
  176712. S. ZEHANI AND G. GELBARD, NOUV. J. CHEM., 0, 511 ( 1986) . REDUCTIONS BY NADH ANALOGS: MECHANISM AND USE IN SYNTHESIS. A REVIEW.a
  176713. GABRIEL WEATHERHEAD
  176714. 12050
  176715. 13059N
  176716. 2/28/96V
  176717. M. FOLLET, CHEM. IND (LONDON), 123 (1986). USE OF COMPLEXES OF DIBORANE AND ORGANOBORANES ON A LABORATORY AND INDUSTRIAL SCALE. A REVIEW.a
  176718. GABRIEL WEATHERHEAD
  176719. 12051
  176720. 13060N
  176721. 2/28/96V{G.W. KABALKA, J. ORGANOMETALL. CHEM., 298, 1 (1986). BORON: BORANES IN ORGANIC SYNTHESIS: ANNUAL SURVEY FOR 1983. A REVIEW.a
  176722. GABRIEL WEATHERHEAD
  176723. 12052
  176724. 13061N
  176725. 2/28/96VzR.V. HOFFMAN, ORG. PREP. PROCED. INT., 18, 181 (1986) . THE OXIDATION OF ELECTRON DONORS WITH SULFONYL PEROXIDES A REVIEW.a
  176726. GABRIEL WEATHERHEAD
  176727. 12053
  176728. 13062N
  176729. 2/28/96VjM. MADESCLAIRE, TETRAHEDRON, 42, 5459 (1986). SYNTHESIS OF SULFOXIDES BY OXIDATION OF THIOETHERS A REVIEW.a
  176730. GABRIEL WEATHERHEAD
  176731. 12054
  176732. 13063N
  176733. 2/28/96
  176734. VpR.M. MORIARTY AND O. PRAKASH, ACC. CHEM. RES. 9, 244 ( 1986) . HYPERVALENT IODINE IN ORGANIC SYNTHESIS A REVIEW.a
  176735. GABRIEL WEATHERHEAD
  176736. 12055
  176737. 13064N
  176738. 2/28/96VtA. PFENNINGER, SYNTHESIS, 89 (1986). ASYMMETRIC EPOXIDATION OF ALLYLIC ALCOHOLS: THE SHARPLESS EPOXIDATION A REVIEW.a
  176739. GABRIEL WEATHERHEAD
  176740. 12056
  176741. 13065N
  176742. 2/28/96V
  176743. H. FIROUZABADI, N. IRANPOOR, F. KIAEEZADEH AND J. TOOFAN, TETRAHEDRON, 42, 719 (1986). COMPARISON OF SOME CR(VL) BASED OXIDANTS A REVIEW.a
  176744. GABRIEL WEATHERHEAD
  176745. 12057
  176746. 13066N
  176747. 2/28/96V
  176748. T. NAKAI AND K. MIKAMI, CHEM. REV., 86, 885 (1986). [ 2,3 ]   WITTIG SIGMATROPIC REARRANGEMENTS IN ORGANIC SYNTHESIS. A REVIEW.a
  176749. GABRIEL WEATHERHEAD
  176750. 12058
  176751. 13067N
  176752. 2/28/96VtG.P. CHIUSOLI, J. ORGANOMET. CHEM., 300, 57 (1986). GROUP VIII METAL CATALYZED C C BOND FORMING SEQUENCES. A REVIEW.a
  176753. GABRIEL WEATHERHEAD
  176754. 12059
  176755. 13068N
  176756. 2/28/96
  176757. VdH.B. KAGAN AND J.L. NAMY, TETRAHEDRON, 42, 6573 (1986).  LANTHANIDES IN ORGANIC SYNTHESIS. A REVIEW.a
  176758. GABRIEL WEATHERHEAD
  176759. 12060
  176760. 13069N
  176761. 2/28/96VdJ. TSUJI, J. ORGANOMET. CHEM., 300, 281 (1986). 25 YEARS IN THE ORGANIC CHEMISTRY OF LEAD. A REVIEW.a
  176762. GABRIEL WEATHERHEAD
  176763. 12061
  176764. 13070N
  176765. 2/28/96VcJ. WOTTER AND 0. DE VOS, J. ORGANOMET. CHEM., 313, 413 (1986). ANNUAL SURVEY: LEAD (1983) A REVIEW.a
  176766. GABRIEL WEATHERHEAD
  176767. 12062
  176768. 13071N
  176769. 2/28/96V
  176770. A. KRIEF, TOP. CURR. CHEM., 135, 1 (1986). SYNTHESIS AND SYNTHETIC APPLICATIONS OF 1 METALLO 1 SELENOCYCLOPROPANES AND  CYCLOBUTANES AND RELATED 1 METALLO 1 SILYLCYCLOPROPANES. A REVIEW.a
  176771. GABRIEL WEATHERHEAD
  176772. 12063
  176773. 13072N
  176774. 2/28/96V
  176775. T.A. BLUMENKOPF AND L.E. OVERMAN, CHEM. REV., 86, 857 (1986). VINYLSILANE  AND ALKYNYLSILANE   TERMINATED CYCLIZATION REACTIONS. A REVIEW.a
  176776. GABRIEL WEATHERHEAD
  176777. 12064
  176778. 13073N
  176779. 2/28/96
  176780. M. ROSENBLUM, J. ORGANOMET. CHEM., 300, 191 (1986). THE CHEMISTRY OF DICARBONYLCYCLOPENTADIENYLIRON COMPLEXES: PROGRESS AND PROSPECTS. A REVIEW.a
  176781. GABRIEL WEATHERHEAD
  176782. 12065
  176783. 13074N
  176784. 2/28/96V
  176785. U.M. DZHEMILEV ET AL., J. 0RGANOMET. CHEM., 304, 17 (1986). HOMOGENEOUS ZIRCONIUM BASED CATALYSTS IN ORGANIC SYNTHESIS. A REVIEW.a
  176786. GABRIEL WEATHERHEAD
  176787. 12066
  176788. 13075N
  176789. 2/28/96VqU.M. DZHEMILEV ET AL., RUSS. CHEM. REV., 55, 66 (1986). ZIRCONIUM COMPLEXES IN SYNTHESIS AND CATALYSIS. A REVIEW.a
  176790. GABRIEL WEATHERHEAD
  176791. 12067
  176792. 13076N
  176793. 2/28/96V
  176794. ANNUAL SURVEY: ORGANIC REACTIONS OF SELECTED PI  COMPLEXES (1984) . Y. YAMAMOTO, ANGEW. CHEM., INT. ED. ENGL., 25, 947 (1986). SELECTIVE SYNTHESIS BY USE OF LEWIS ACIDS IN THE PRESENCE OF ORGANOCOPPER AND RELATED REAGENTS. A REVIEW.a
  176795. GABRIEL WEATHERHEAD
  176796. 12068
  176797. 13077N
  176798. 2/28/96VIB.W. ROCKETT AND G. MARR, J. ORGANOMET. CHEM., 305, 199 (1986). A REVIEW.a
  176799. GABRIEL WEATHERHEAD
  176800. 12069
  176801. 13078N
  176802. 2/28/96V
  176803. J. TSUJI, TETRAHEDRON, 42, 4361 (1986). NEW GENERAL SYNTHETIC METHODS INVOLVING PI  ALLYLPALLADIUM COMPLEXES AS INTERMEDIATES AND NEUTRAL REACTION CONDITIONS. A REVIEW.a
  176804. GABRIEL WEATHERHEAD
  176805. 12070
  176806. 13079N
  176807. 2/28/96VxJ. TSUJI, PURE APPL. CHEM., 58, 869 (1986). LECTURE: NEW SYNTHETIC REACTIONS CATALYZED BY PALLADIUM COMPLEXES. A REVIEW.a
  176808. GABRIEL WEATHERHEAD
  176809. 12071
  176810. 13080N
  176811. 2/28/96V
  176812. J. K. STILLE, ANGEW.CHEM., INT. ED. ENGL., 25, 508 (1986). THE PALLADIUM   CATALYZED CROSS   COUPLING REACTIONS OF ORGANOTIN REAGENTS WITH ORGANIC ELECTROPHILES. A REVIEW.a
  176813. GABRIEL WEATHERHEAD
  176814. 12072
  176815. 13081N
  176816. 2/28/96VqT.M. MITCHELL, J. ORGANOMET. CHEM., 304, 1 (1986). TRANSITION   METAL CATALYSIS IN ORGANOTIN CHEMISTRY. A REVIEW.a
  176817. GABRIEL WEATHERHEAD
  176818. 12073
  176819. 13082N
  176820. 2/28/96V
  176821. S. SIVARAM ET AL., CHEM REV., 86, 353 (1986). DIMERIZATION OF ETHYLENE AND PROPYLENE CATALYZED BY TRANSITION   METAL COMPLEXES. A REVIEW.
  176822. GABRIEL WEATHERHEAD
  176823. 12074
  176824. 13083N
  176825. 2/28/96V
  176826. G. JAOUEN, PURE APPL. CHEM., 58, 597 (1986). LECTURE: THE EFFECT OF TRANSITION METAL BENZYL AND PROPARGYL SPECIES ON THE BEHAVIOR OF STEROIDAL HORMONES. A REVIEW.a
  176827. GABRIEL WEATHERHEAD
  176828. 12075
  176829. 13084N
  176830. 2/28/96VvH. BRUNNER, J. ORGANOMET. CHEM., 300, 39 (1986). ENANTIOSELECTIVE CATALYSIS WITH TRANSITION METAL COMPLEXES. A REVIEW.a
  176831. GABRIEL WEATHERHEAD
  176832. 12076
  176833. 13085N
  176834. 2/28/96VmA. YAMAMOTO, J. ORGANOMET. CHEM., 300, 347 (1986). TRANSITION METAL ALKYLS, A PERSONAL PERSPECTIVE. A REVIEW.a
  176835. GABRIEL WEATHERHEAD
  176836. 12077
  176837. 13086N
  176838. 2/28/96V
  176839. B.M. TROST, J. ORGANOMET. CHEM., 300, 263 (1986). TRANSITION METALS AND OLEFINS. A PROMISING LAND: A PERSONAL ACCOUNT. A REVIEW.a
  176840. GABRIEL WEATHERHEAD
  176841. 12078
  176842. 13087N
  176843. 2/28/96V
  176844. J. HALPERN, PURE APPL. CHEM., 58, 575 (1986). LECTURE: FREE RADICAL MECHANISMS IN ORGANOMETALLIC AND BIOORGANOMETALLIC CHEMISTRY. A REVIEW.a
  176845. GABRIEL WEATHERHEAD
  176846. 12079
  176847. 13088N
  176848. 2/28/96V
  176849. L. MARKO, J. ORGANOMET CHEM., 305, 333 (1986). REVIEW; TRANSITION METALS IN ORGANIC SYNTHESIS: HYDROFORMYLATION, REDUCTION AND OXIDATION. ANNUAL SURVEY COVERING THE YEAR 1984. A REVIEW.a
  176850. GABRIEL WEATHERHEAD
  176851. 12080
  176852. 13089N
  176853. 2/28/96VyH. ALPER, J. ORGANOMET. CHEM., 300, 1 (1986). HOMOGENEOUS AND PHASE TRANSFER CATALYZED CARBONYLATION REACTIONS. A REVIEW.a
  176854. GABRIEL WEATHERHEAD
  176855. 12081
  176856. 13090N
  176857. 2/28/96V
  176858. A. SUZUKI, PURE APPL. CHEM., 58, 629 (1986). LECTURE: NEW APPLICATIONS OF ORGANOBORON COMPOUNDS IN ORGANIC SYNTHESIS. A REVIEW.a
  176859. GABRIEL WEATHERHEAD
  176860. 12082
  176861. 13091N
  176862. 2/28/96V
  176863. M. FOLLET, CHEM. IND., 123 (1986). USE OF COMPLEXES OF DIBORANE AND ORGANOBORANES ON A LABORATORY AND INDUSTRIAL SCALE. A REVIEW.a
  176864. GABRIEL WEATHERHEAD
  176865. 12083
  176866. 13092N
  176867. 2/28/96
  176868. H.W. MOORE AND O.H.W. DECKER, CHEM. REV., 86, 821 (1986). CONJUGATED KETENES: NEW ASPECTS OF THEIR SYNTHESIS AND SELECTED UTILITY FOR THE SYNTHESIS OF PHENOLS, HYDROQUINONES AND QUINONES. A REVIEW.a
  176869. GABRIEL WEATHERHEAD
  176870. 12084
  176871. 13093N
  176872. 2/28/96VnM. TISLER, ORG. PREP. PROCED. INT., 18, 19 (1986). SYNTHETIC APPROACHES TO BINAPHTHALENES. A REVIEW. A REVIEW.a
  176873. GABRIEL WEATHERHEAD
  176874. 12085
  176875. 13094N
  176876. 2/28/96V
  176877. R. BOLTON AND G. H. WILLIAMS, CHEM. SOC. REV., 15, 261 (1986). HOMOLYTIC ARYLATION OF AROMATIC AND POLYFLUOROAROMATIC COMPOUNDS. A REVIEW.a
  176878. GABRIEL WEATHERHEAD
  176879. 12086
  176880. 13095N
  176881. 2/28/96V
  176882. M. KARPF, ANGEW. CHEM., INT. ED. ENGL., 25, 414 (1986). 0RGANIC SYNTHESIS AT HIGH TEMPERATURES. GAS PHASE FLOW THERMOLYSIS. A REVIEW.a
  176883. GABRIEL WEATHERHEAD
  176884. 12087
  176885. 13096N
  176886. 2/28/96
  176887. F. FRINGUELLI, A. TATICCHI, E. WENKERT ET AL., J. ORG. CHEM., 51, 5177 (1986). DIELS ALDER REACTIONS OF CYCLOALKENONES. 11. REGIOSELECTIVITY OF 2 CYCLOHEXENONES. A REVIEW.a
  176888. GABRIEL WEATHERHEAD
  176889. 12088
  176890. 13097N
  176891. 2/28/96V
  176892. W.V. DOWER AND K .P. C. VOLLHARDT, TETRAHEDRON, 42, 1873 (1986). THERMAL CONVERSION OF 1,5,9 TRIYNES. [ 2+2+2 ] CYCLOADDITIONS OR [ 3,3 ] SIGMATROPIC SHIFTS. A REVIEW.a
  176893. GABRIEL WEATHERHEAD
  176894. 12089
  176895. 13098N
  176896. 2/28/96V
  176897. J.W. SCHEEREN, REC. TRAV. CHIM., 105, 71 (1986). SYNTHETIC AND MECHANISTIC ASPECTS OF THERMAL (2+2) CYCLOADDITIONS OF KETENE ACETALS WITH ELECTRON POOR ALKENES AND CARBONYL COMPOUNDS. A REVIEW.a
  176898. GABRIEL WEATHERHEAD
  176899. 12090
  176900. 13099N
  176901. 2/28/96VuL.A. PAQUETTE, CHEM. REV., 86, 733 (1986). SILYL SUBSTITUTED CYCLOPROPANES AS VERSATILE SYNTHETIC REAGENTS. A REVIEW.a
  176902. GABRIEL WEATHERHEAD
  176903. 12091
  176904. 13100N
  176905. 2/28/96
  176906. H. MEIER ET AL., TETRAHEDRON, 42, 1711 (1986). STRAINED CYCLOALKENYNES. CARBENE OR CARBENOID ADDITIONS TO A MULTIPLE BOND A REVIEW.a
  176907. GABRIEL WEATHERHEAD
  176908. 12092
  176909. 13101N
  176910. 2/28/96V
  176911. B.M. TROST, ANGEW. CHEM., INT. ED. ENGL., 25, 1 (1986). [ 3 + 2 ] CYCLOADDITION APPROACHES TO 5 MEMBERED RINGS VIA TRIMETHYLENEMETHANE AND ITS EQUIVALENTS. A REVIEW.a
  176912. GABRIEL WEATHERHEAD
  176913. 12093
  176914. 13102N
  176915. 2/28/96V
  176916. J. SIMONET AND G. LE GUILLANTON, BULL. SOC. CHIM. FR., 221 (1986). CYCLIZATION BY ELECTROCHEMICAL ACTIVATION. I. INTRAMOLECULAR REACTIONS. A REVIEW.a
  176917. GABRIEL WEATHERHEAD
  176918. 12094
  176919. 13103N
  176920. 2/28/96V
  176921. M.P. DOYLE, ACC. CHEM. RES., 19, 348 (1986). ELECTROPHILIC METAL CARBENES AS REACTION INTERMEDIATES IN CATALYTIC REACTIONS. A REVIEW.a
  176922. GABRIEL WEATHERHEAD
  176923. 12095
  176924. 13104N
  176925. 2/28/96
  176926. P.L. FUCHS AND T.F. BRAISH, CHEM. REV., 86, 903 (1986). MULTIPLY CONVERGENT SYNTHESES VIA CONJUGATE ADDITION REACTIONS TO CYCLOALKENYL SULFONES. CONJUGATE ADDITIONS OF ORGANOMETALLIC REAGENTS A REVIEW.a
  176927. GABRIEL WEATHERHEAD
  176928. 12096
  176929. 13105N
  176930. 2/28/96V}G.R. NEWKOME AND G.R. BAKER, ORG. PREP. PROCED. INT., 18, 119 (1986). THE CHEMISTRY OF METHANETRICARBOXYLIC ESTERS. A REVIEW.a
  176931. GABRIEL WEATHERHEAD
  176932. 12097
  176933. 13106N
  176934. 2/28/96V
  176935. T. MUKAIYAMA, PURE APPL. CHEM., 58, 505 (1986). TIN (II) COMPOUNDS AS SYNTHETIC CONTROL ELEMENTS IN ORGANIC SYNTHESIS. A REVIEW.a
  176936. GABRIEL WEATHERHEAD
  176937. 12098
  176938. 13107N
  176939. 2/28/96
  176940. R.E. GAWLEY ET AL. ,IBID, 5L, 3076 (1986).  OXYGEN  AND NITROGEN  ASSISTED LITHIATION AND CARBOLITHIATION OF NON AROMATIC COMPOUNDS; PROPERTIES OF NON AROMATIC ORGANOLITHIUM COMPOUNDS CAPABLE OF INTRAMOLECULAR COORDINATION TO OXYGEN AND NITROGEN.' A REVIEW.
  176941. GABRIEL WEATHERHEAD
  176942. 12099
  176943. 13108N
  176944. 2/28/96
  176945. G.W. KLUMPP, REC. TRAV. CHIM., 105, 1 (1986). FOR EXAMPLES SEE: A.I. MEYERS AND T. R. BAILEY, J. ORG. CHEM., 51, 872 (1986); A REVIEW.a
  176946. GABRIEL WEATHERHEAD
  176947. 12100
  176948. 13109N
  176949. 2/28/96VhR. PARDO AND M. SANTELLI, BULL. CHIM. SOC. FR., 98 (1985). SYNTHESIS OF VITAMIN D METABOLITES. A REVIEW.a
  176950. GABRIEL WEATHERHEAD
  176951. 12101
  176952. 13110N
  176953. 2/28/96V
  176954. K. WIESNER, TETRAHEDRON, 41, 485 (1985). SOME HIGHLIGHTS IN THE STRUCTURAL AND SYNTHETIC CHEMISTRY OF THE ACONITE ALKALOIDS. A REVIEW.a
  176955. GABRIEL WEATHERHEAD
  176956. 12102
  176957. 13111N
  176958. 2/28/96VvM.J. BROADHURST, C.H. HASSALL AND G.J. THOMAS, CHEM. IND. (LONDON), 106 (1985). SYNTHESIS OF ANTHRACYCLINES. A REVIEW.a
  176959. GABRIEL WEATHERHEAD
  176960. 12103
  176961. 13112N
  176962. 2/28/96V
  176963. P. J. SCHEUER, TETRAHEDRON, 41, 979 (1985). THE ORGANIC CHEMISTRY OF MARINE NATURAL PRODUCTS. (SYMPOSIUM IN PRINT   14 PAPERS) A REVIEW.a
  176964. GABRIEL WEATHERHEAD
  176965. 12104
  176966. 13113N
  176967. 2/28/96
  176968. F. PIETRA, GAZZ. CHIM. ITAL., 115, 443 (1985). TOTAL SYNTHESIS OF MARINE NATURAL PRODUCTS: A POWERFUL CONTRIBUTION TO THE UNDERSTANDING AND DEVELOPMENT OF MARINE ORGANIC CHEMISTRY. A REVIEW.a
  176969. GABRIEL WEATHERHEAD
  176970. 12105
  176971. 13114N
  176972. 2/28/96V
  176973. M. VANDEWALLE AND P. DE CLERCQ, TETRAHEDRON, 41, 1767 (1985). THE TOTAL SYNTHESIS OF POLYCARBOCYCLIC SESQUITERPENES. A SURVEY OF NOVEL METHODS AND REACTIONS. A REVIEW.a
  176974. GABRIEL WEATHERHEAD
  176975. 12106
  176976. 13115N
  176977. 2/28/96V
  176978. M. YALPANI, TETRAHEDRON, 41, 2957 (1985). A SURVEY OF RECENT ADVANCES IN SELECTIVE CHEMICAL AND ENZYMIC POLYSACCHARIDE MODIFICATIONS. A REVIEW.a
  176979. GABRIEL WEATHERHEAD
  176980. 12107
  176981. 13116N
  176982. 2/28/96V
  176983. R.M WENGER, ANGEW. CHEM., INT. ED. ENGL., 24, 77 (1985). SYNTHESIS OF CYCLOSPORINE AND ANALOGUES: STRUCTURAL REQUIREMENTS FOR IMMUNOSUPPRESIVE ACTIVITY. A REVIEW.a
  176984. GABRIEL WEATHERHEAD
  176985. 12108
  176986. 13117N
  176987. 2/28/96
  176988. H. MILLAUER, W. SCHWERTFEGER AND G. SIEGEMUND, ANGEW. CHEM. INT. ED. ENGL., 24, 161 (1985). HEXAFLUOROPROPENE OXIDE   A KEY COMPOUND IN ORGANOFLUORINE CHEMISTRY. A REVIEW.a
  176989. GABRIEL WEATHERHEAD
  176990. 12109
  176991. 13118N
  176992. 2/28/96VlL. DOLBY GLOVER, SPEC. CHEM., 5, 4 (1985). SPECIALITY INTERMEDIATES   THE ROLE OF FLUOROAROMATICS. A REVIEW.a
  176993. GABRIEL WEATHERHEAD
  176994. 12110
  176995. 13119N
  176996. 2/28/96V
  176997. T. N. GERASIMOVA AND N.A. ORLOVA, J. FLUOR. CHEM., 28, 361 (1985). SYNTHESIS OF 1,2 DISUBSTITUTED POLYFLUOROBENZENES. A REVIEW.a
  176998. GABRIEL WEATHERHEAD
  176999. 12111
  177000. 13120N
  177001. 2/28/96V_H. VYPLEL. CHIMIA, 39, 305 (1985). PREPARATIVE FLUORINATIONS WITH MOLECULAR FLUORINE. A REVIEW.a
  177002. GABRIEL WEATHERHEAD
  177003. 12112
  177004. 13121N
  177005. 2/28/96V}A. HAAS AND M. LIEB, CHIMIA. 39, 134 (1985). MODERN SYNTHETIC PROCEDURES FOR THE FLUORINATION OF ORGANIC MOLECULES. A REVIEW.a
  177006. GABRIEL WEATHERHEAD
  177007. 12113
  177008. 13122N
  177009. 2/28/96
  177010. VvS. ROZEN AND R. FILLER, TETRAHEDRON, 41, 1111 (1985).  ALPHA FLUOROCARBONYL COMPOUNDS AND RELATED CHEMISTRY. A REVIEW.a
  177011. GABRIEL WEATHERHEAD
  177012. 12114
  177013. 13123N
  177014. 2/28/96V
  177015. R.A. CHERKASOV, G.A. KUTYREV AND A.N. PUDOVIK, TETRAHEDRON, 41, 2567 (1985). ORGANOTHIOPHOSPHORUS REAGENTS IN ORGANIC SYNTHESIS. A REVIEW.a
  177016. GABRIEL WEATHERHEAD
  177017. 12115
  177018. 13124N
  177019. 2/28/96VjL. ENGMAN, ACC. CHEM. RES., 18, 274 (1985). SYNTHETIC APPLICATIONS OF ORGANOTELLURIUM DHEMISTRY. A REVIEW.a
  177020. GABRIEL WEATHERHEAD
  177021. 12116
  177022. 13125N
  177023. 2/28/96V
  177024. M.R. BRYCE, ALDRICHIMICA ACTA, 18, 73 (1985). TETRATHIAFULVALENES (TTF) AND THEIR SELENIUM AND TELLURIUM ANALOGS (TSF AND TTEF): ELECTRON DONORS FOR ORGANIC MOLECULES. A REVIEW.a
  177025. GABRIEL WEATHERHEAD
  177026. 12117
  177027. 13126N
  177028. 2/28/96V
  177029. D. LIOTTA, TETRAHEDRON, 41, 4727 (1985). RECENT ASPECTS OF ORGANOSELENIUM CHEMISTRY. (SYMPOSIUM IN PRINT   17 PAPERS) A REVIEW.a
  177030. GABRIEL WEATHERHEAD
  177031. 12118
  177032. 13127N
  177033. 2/28/96
  177034. K.C. NICOLAOU, N.A. PETASIS AND D.A. CLAREMON, TETRAHEDRON, 41, 4835 (1985). N PHENYLSELENOPHTHALIMIDE (NPSP) A VALUABLE SELENENYLATING AGENT. A REVIEW.a
  177035. GABRIEL WEATHERHEAD
  177036. 12119
  177037. 13128N
  177038. 2/28/96V
  177039. S. Y. LEY, CHEM. IND.(LONDON), 101 (1985). SYNTHETIC APPLICATIONS OF YNES, ENES AND ONES. ORGANOSELENIUM MEDIATED CYCLIZATION REACTIONS IN ORGANIC SYNTHESIS. A REVIEW.a
  177040. GABRIEL WEATHERHEAD
  177041. 12120
  177042. 13129N
  177043. 2/28/96V
  177044. K. MARUOKA AND H. YAMAMOTO, ANGEW. CHEM. LNT. ED. ENGL., 24, 668 (1985). SELECTIVE REACTIONS USING ORGANOALUMINUM CHEMISTRY. A REVIEW.a
  177045. GABRIEL WEATHERHEAD
  177046. 12121
  177047. 13130N
  177048. 2/28/96VgH.C. BROWN, ISRAEL J. CHEM., 25, 84 (1985). THE BORANE ADVENTURE   PAST, PRESENT, AND FUTURE. A REVIEW.a
  177049. GABRIEL WEATHERHEAD
  177050. 12122
  177051. 13131N
  177052. 2/28/96V
  177053. S. DAVID AND S. HANESSIAN, TETRAHEDRON, 41, 643 (1985). REGIOSELECTIVE MANIPULATION OF HYDROXYL GROUPS VIA ORGANOTIN DERIVATIVES. A REVIEW.a
  177054. GABRIEL WEATHERHEAD
  177055. 12123
  177056. 13132N
  177057. 2/28/96VTR. MULLER, Z. CHEM., 25, 309 (1985). THE CHEMISTRY OF ORGANOCHLOROSILANES. A REVIEW.a
  177058. GABRIEL WEATHERHEAD
  177059. 12124
  177060. 13133N
  177061. 2/28/96VqI. KUWAJIMA AND E. NAKAMURA, ACC. CHEM. RES., 8, 181 (1985). 
  177062. REACTIVE ENOLATES FROM SILYL ENOL ETHERS. A REVIEW.a
  177063. GABRIEL WEATHERHEAD
  177064. 12125
  177065. 13134N
  177066. 2/28/96VdR. ANDERSON, SYNTHESIS, 717 (1985). SYNTHETIC APPLICATIONS OF CHLOROMETHYLTRIMETHYLSILANE. A REVIEW.a
  177067. GABRIEL WEATHERHEAD
  177068. 12126
  177069. 13135N
  177070. 2/28/96V
  177071. B. GIESE, ANGEW. CHEM., INT. ED. ENGL., 24, 553 (1985). SYNTHESES WITH RADICALS   C C BOND FORMATION VIA ORGANOTIN AND ORGANOMERCURY COMPOUNDS. A REVIEW.a
  177072. GABRIEL WEATHERHEAD
  177073. 12127
  177074. 13136N
  177075. 2/28/96V[A. RYABOV, SYNTHESIS, 233 (1985). CYCLOPALLADATED COMPLEXES IN ORGANIC SYNTHESIS. A REVIEW.a
  177076. GABRIEL WEATHERHEAD
  177077. 12128
  177078. 13137N
  177079. 2/28/96
  177080. H. BONNEMANN, ANGEW. CHEM., INT. ED. ENGL., 24, 248 (1985). ORGANOCOBALT COMPOUNDS IN THE SYNTHESIS OF PYRIDINES   AN EXAMPLE OF STRUCTURE EFFECTIVITY RELATIONSHIP IN HOMOGENEOUS CATALYSIS. A REVIEW.a
  177081. GABRIEL WEATHERHEAD
  177082. 12129
  177083. 13138N
  177084. 2/28/96V
  177085. E. NEGISHI AND T. TAKAHASHI, ALDRICHIMICA ACTA, 8, 31 (1985). ORGANOZIRCONIUM COMPOUNDS AS NEW REAGENTS AND INTERMEDIATES. A REVIEW.a
  177086. GABRIEL WEATHERHEAD
  177087. 12130
  177088. 13139N
  177089. 2/28/96VhP.L. WATSON AND G.W. PARSHALL, ACC. CHEM. PES., 18, 51 (1985). ORGANOLANTHANIDES IN CATALYSIS. A REVIEW.a
  177090. GABRIEL WEATHERHEAD
  177091. 12131
  177092. 13140N
  177093. 2/28/96VXJ.R. LANG, ALDRICHIMICA ACTA, 18, 87 (1985). LANTHANIDES IN ORGANIC SYNTHESIS. A REVIEW.a
  177094. GABRIEL WEATHERHEAD
  177095. 12132
  177096. 13141N
  177097. 2/28/96
  177098. B. BOGDANOVIC, ANGEW. CHEM. INT. ED; ENGL., 24, 262 (1985). CATALYTIC SYNTHESIS OF ORGANOLITHIUM AND ORGANOMAGNESIUM COMPOUNDS AND OF LITHIUM AND MAGNESIUM HYDRIDES   APPLICATIONS IN ORGANIC SYNTHESIS AND HYDROGEN STORAGE. A REVIEW.a
  177099. GABRIEL WEATHERHEAD
  177100. 12133
  177101. 13142N
  177102. 2/28/96V
  177103. M. SEMMELHACK, TETRAHEDRON, 41, 5741 (1985). APPLICATION OF NEWER ORGANOMETALLIC REAGENTS TO THE TOTAL SYNTHESIS OF NATURAL PRODUCTS. (SYMPOSIUM IN PRINT   L8 PAPERS) A REVIEW.a
  177104. GABRIEL WEATHERHEAD
  177105. 12134
  177106. 13143N
  177107. 2/28/96V~F. PETIT, BULL. SOC. CHIM. FR., 203 (1985). ORGANIC CHEMISTRY MEDIATED BY ELECTROREDUCED TRANSITION METAL COMPLEXES. A REVIEW.a
  177108. GABRIEL WEATHERHEAD
  177109. 12135
  177110. 13144N
  177111. 2/28/96V]R.H. CRABTREE, CHEM. REV., 85, 245 (1985). THE ORGANOMETALLIC CHEMISTRY OF ALKANES. A REVIEW.a
  177112. GABRIEL WEATHERHEAD
  177113. 12136
  177114. 13145N
  177115. 2/28/96
  177116. C. NARAYANA AND M. PERIASAMY. SYNTHESIS, 253 (1985). ORGANIC SYNTHESIS VIA CARBONYLATION OF ORGANOMETALLIC REAGENTS WITH CARBON MONOXIDE. A REVIEW.a
  177117. GABRIEL WEATHERHEAD
  177118. 12137
  177119. 13146N
  177120. 2/28/96V\T. L. HO, TETRAHEDRON, 41, 1 (1985). CHEMOSELECTIVITY OF ORGANOMETALLIC REACTIONS. A REVIEW.a
  177121. GABRIEL WEATHERHEAD
  177122. 12138
  177123. 13147N
  177124. 2/28/96VmN. BALASUFRAMANIAN, ORG. PREP. PROC. INT., 7, 25 (1985). RECENT SYNTHETIC APPLICATIONS OF NITRONES. A REVIEW.a
  177125. GABRIEL WEATHERHEAD
  177126. 12139
  177127. 13148N
  177128. 2/28/96V
  177129. I. SAITO AND T. MATSUURA, TETRAHEDRON, 41, 2037 (1985). RECENT ASPECTS OF SINGLET OXYGEN CHEMISTRY OF PHOTOOXIDATION. (SYMPOSIUM IN PRINT   24 PAPERS) A REVIEW.a
  177130. GABRIEL WEATHERHEAD
  177131. 12140
  177132. 13149N
  177133. 2/28/96VwM. PLATZ, TETRAHEDRON, 41, 1423 (1985). RECENT ASPECTS OF CARBENE CHEMISTRY. (SYMPOSIUM IN PRINT   20 PAPERS) A REVIEW.a
  177134. GABRIEL WEATHERHEAD
  177135. 12141
  177136. 13150N
  177137. 2/28/96
  177138. C. BOTTEGHI AND F. SOCCOLINI, SYNTHESIS, 592 (1985). MALONALDEHYDE, SUCCINALDEHYDE AND GLUTARALDEHYDE MONOACETALS: SYNTHESES AND APPLICATIONS. A REVIEW.a
  177139. GABRIEL WEATHERHEAD
  177140. 12142
  177141. 13151N
  177142. 2/28/96V
  177143. L. BAIOCCHI ET AL., GAZZ. CHIM. ITAL., 115, 199 (1985). ARENES FROM ALKANES OR CYCLOALKANES THROUGH DEHYDRATION OR REARRANGEMENT WITH PYRIDINIUM CHLORIDE. A REVIEW.a
  177144. GABRIEL WEATHERHEAD
  177145. 12143
  177146. 13152N
  177147. 2/28/96V
  177148. J. E. MILLS, C. A. MARYANOFF ET AL., ORG. PREP. PROC. INT., 6, 97 (1984). THE REACTION OF AMINES WITH METHYLENE CHLORIDE. A REVIEW.a
  177149. GABRIEL WEATHERHEAD
  177150. 12144
  177151. 13153N
  177152. 2/28/96V
  177153. A. YOSHIKOSHI AND M. MIYASHITA, ACC. CHEM. RES., 8, 284 (1985). OXOALKYLATION OF CARBONYL COMPOUNDS WITH CONJUGATED NITRO OLEFINS. A REVIEW.a
  177154. GABRIEL WEATHERHEAD
  177155. 12145
  177156. 13154N
  177157. 2/28/96V
  177158. B. GIESE, TETRAHEDRON, 41, 3887 (1985). SELECTIVITY AND SYNTHETIC APPLICATIONS OF RADICAL REACTIONS. (SYMPOSIUM IN PRINT   29 PAPERS) A REVIEW.
  177159. GABRIEL WEATHERHEAD
  177160. 12146
  177161. 13155N
  177162. 2/28/96V
  177163. W. OPPOLZER, TETRAHEDRON, 41, 3447 (1985). SYNTHETIC APPLICATIONS OF DIPOLAR CYCLOADDITION REACTIONS. (SYMPOSIUM IN PRINT   11 PAPERS) A REVIEW.a
  177164. GABRIEL WEATHERHEAD
  177165. 12147
  177166. 13156N
  177167. 2/28/96V~M. C. LASNE AND J. L. RIPOLL, SYNTHESIS, 121 (1985). NEW SYNTHETIC DEVELOPMENTS OF THE [4 PI + 2 PI] CYCLOREVERSION. A REVIEW.a
  177168. GABRIEL WEATHERHEAD
  177169. 12148
  177170. 13157N
  177171. 2/28/96V
  177172. S. MASAMUNE. W. CHOY, J.S. PETERSEN AND L.R. SITA, ANGEW. CHEM., INT. ED. ENGL., 24, 1 (1985). DOUBLE ASYMMETRIC SYNTHESIS AND A NEW STRATEGY FOR STEREOCHEMICAL CONTROL IN ORGANIC SYNTHESIS. A REVIEW.a
  177173. GABRIEL WEATHERHEAD
  177174. 12149
  177175. 13158N
  177176. 2/28/96V
  177177. H. SIMON ET AL., ANGEW. CHEM., INT. ED. ENGL., 24, 539 (1985). CHIRAL COMPOUNDS SYNTHESIZED BY BIOCATALYTIC REDUCTIONS. A REVIEW.a
  177178. GABRIEL WEATHERHEAD
  177179. 12150
  177180. 13159N
  177181. 2/28/96
  177182. V`S. GRONOWITZ, CHEM. SCRIPTA, 25 (1985). NOBEL SYMPOSIUM: ASYMMETRIC ORGANIC SYNTHESIS. A REVIEW.a
  177183. GABRIEL WEATHERHEAD
  177184. 12151
  177185. 13160N
  177186. 2/28/96V`A. TALLEC, BULL. SOC. CHIM. FR., 743 (1985). ASYMMETRIC SYNTHESIS BY ELECTROCHEMISTRY. A REVIEW.a
  177187. GABRIEL WEATHERHEAD
  177188. 12152
  177189. 13161N
  177190. 2/28/96VtR. BOWEN AND S. PUGH, CHEM. IND.(LONDON), 323 (1985). REDOX ENZYMES IN INDUSTRIAL FINE CHEMICAL SYNTHESES. A REVIEW.a
  177191. GABRIEL WEATHERHEAD
  177192. 12153
  177193. 13162N
  177194. 2/28/96V
  177195. G.M. WHITESIDES AND C. H. WONG, ANGEW. CHEM. INT. ED. ENGL., 24, 617 (1985). ENZYMES AS CATALYSTS IN SYNTHETIC ORGANIC CHEMISTRY. A REVIEW.a
  177196. GABRIEL WEATHERHEAD
  177197. 12154
  177198. 13163N
  177199. 2/28/96V
  177200. P. HODGE AND D.C. SHERRINGTON, BRIT. POLYMER. J., 6, 163 (1984). SECOND INTERNATIONAL SYMPOSIUM ON POLYMER SUPPORTED REACTIONS IN ORGANIC CHEMISTRY. A REVIEW.a
  177201. GABRIEL WEATHERHEAD
  177202. 12155
  177203. 13164N
  177204. 2/28/96
  177205. C. E. PEISHOFF AND W. L. JORGENSEN, J. ORG. CHEM., 50, 3174 (1985). COMPUTER ASSISTED MECHANISTIC EVALUATION OF ORGANIC REACTIONS. IO STEREOCHEMISTRY. A REVIEW.a
  177206. GABRIEL WEATHERHEAD
  177207. 12156
  177208. 13165N
  177209. 2/28/96V}B. J. MCARDLE AND J. N. SHERWOOD, CHEM. IND.(LONDON), 268 (1985). THE PURITY AND PURIFICATION OF ORGANIC MATERIALS. A REVIEW.a
  177210. GABRIEL WEATHERHEAD
  177211. 12157
  177212. 13166N
  177213. 2/28/96V
  177214. R. CARLSON, T. LUNDSTEDT AND C. ALBANO, ACTA CHEM. SCAND. B, 39, 79 (1985). SCREENING OF SUITABLE SOLVENTS IN ORGANIC SYNTHESIS. STRATEGIES FOR SOLVENT SELECTION. A REVIEW.a
  177215. GABRIEL WEATHERHEAD
  177216. 12158
  177217. 13167N
  177218. 2/28/96VlK. MATSUMOTO, A. SERA AND T. UCHIDA, SYNTHESIS, 1 (1985). ORGANIC SYNTHESIS UNDER HIGH PRESSURE I. A REVIEW.a
  177219. GABRIEL WEATHERHEAD
  177220. 12159
  177221. 13168N
  177222. 2/28/96VdK. MATSUMOTO AND A. SERA, SYNTHESIS, 999 (1985). ORGANIC SYNTHESIS UNDER HIGH PRESSURE II. A REVIEW.a
  177223. GABRIEL WEATHERHEAD
  177224. 12160
  177225. 13169N
  177226. 2/28/96
  177227. A. RABENAU, ANGEW. CHEM. INT. ED. ENGL., 24, 1026 (1985). THE ROLE OF HYDROTHERMAL SYNTHESIS IN PREPARATIVE CHEMISTRY. A REVIEW.a
  177228. GABRIEL WEATHERHEAD
  177229. 12161
  177230. 13170N
  177231. 2/28/96V
  177232. E. LEETE AND J. PORWOLL, ALDRICHIMICA ACTA, 8, 13 (1985). THE USE OF CARBON 13 LABELED COMPOUNDS IN ORGANIC CHEMISTRY, BIOCHEMISTRY AND MEDICINE. A REVIEW.a
  177233. GABRIEL WEATHERHEAD
  177234. 12162
  177235. 13171N
  177236. 2/28/96V
  177237. J. BAUER, R. HERGES, E. FOUNTAIN AND I. UGI, CHIMIA, 39, 43 (1985). IGOR AND COMPUTER ASSISTED INNOVATION IN CHEMISTRY. A REVIEW.a
  177238. GABRIEL WEATHERHEAD
  177239. 12163
  177240. 13172N
  177241. 2/28/96VrS. TOMA AND V. KALISTA, CHEM. LISTY, 79, 578 (1985). UTILIZATION OF ULTRASOUND IN IN ORGANIC SYNTHESIS.
  177242.  A REVIEW.a
  177243. GABRIEL WEATHERHEAD
  177244. 12164
  177245. 13173N
  177246. 2/28/96VrM.P. CAVA AND M.I. LEVINSON, TETRAHEDRON, 41, 5061 (1985). 'THIONATION REACTIONS OF LAWESSON'S REAGENTS. A REVIEW.a
  177247. GABRIEL WEATHERHEAD
  177248. 12165
  177249. 13174N
  177250. 2/28/96
  177251. VcC.R. JOHNSON, ALDRICHIMICA ACTA, 18, 3 (1985). APPLICATIONS OF SULFOXIMINES IN SYNTHESIS. A REVIEW.a
  177252. GABRIEL WEATHERHEAD
  177253. 12166
  177254. 13175N
  177255. 2/28/96VaJ.D. COYLE, TETRAHEDRON, 41, 5393 (1985). THE PHOTOCHEMISTRY OF THIOCARBONYL COMPOUNDS. A REVIEW.a
  177256. GABRIEL WEATHERHEAD
  177257. 12167
  177258. 13176N
  177259. 2/28/96V
  177260. H.C. HANSEN AND A. SENNING, ORG. PREP. PROC. INT., 7, 275 (1985). REACTIONS OF THIOCARBONYL COMPOUNDS WITH CHLORINE AND WITH SULFUR DIOXIDE. A REVIEW.a
  177261. GABRIEL WEATHERHEAD
  177262. 12168
  177263. 13177N
  177264. 2/28/96VeS. HOARE, SPEC. CHEM., 5 (4), 22 (1985). SYNTHETIC PEPTIDES   FROM MILLIGRAMS TO KILOGRAMS. A REVIEW.a
  177265. GABRIEL WEATHERHEAD
  177266. 12169
  177267. 13178N
  177268. 2/28/96V
  177269. H. D. JAKUBKE, P. KUHL AND A. KONNECKE, ANGEW. CHEM. INT. ED. ENGL., 85, 93 (1985). BASIC PRINCIPLES OF PROTEASE CATALYZED PEPTIDE BOND FORMATION. A REVIEW.a
  177270. GABRIEL WEATHERHEAD
  177271. 12170
  177272. 13179N
  177273. 2/28/96
  177274. VnR.B. MERRIFIELD, ANGEW. CHEM. INT. ED. ENGL., 24, 799 (1985). SOLID PHASE SYNTHESIS (NOBEL LECTURE). A REVIEW.a
  177275. GABRIEL WEATHERHEAD
  177276. 12171
  177277. 13180N
  177278. 2/28/96VWM. ZAORAL, CHEM. LISTY, 79, 860 (1985). PEPTIDE SYNTHESIS IN THE SOLID STATE. A REVIEW.a
  177279. GABRIEL WEATHERHEAD
  177280. 12172
  177281. 13181N
  177282. 2/28/96V
  177283. F.J. RAMIREZ AND J.F. MARACEK, SYNTHESIS, 449 (1985). SYNTHESIS OF PHOSPHODIESTERS: THE CYCLIC ENEDIOL PHOSPHORYL METHOD. A REVIEW.a
  177284. GABRIEL WEATHERHEAD
  177285. 12173
  177286. 13182N
  177287. 2/28/96V
  177288. M. LALONDE AND T.H. CHAN, SYNTHESIS, 817 (1985). USE OF ORGANOSILICON REAGENTS AS PROTECTIVE GROUPS IN ORGANIC SYNTHESIS. A REVIEW.a
  177289. GABRIEL WEATHERHEAD
  177290. 12174
  177291. 13183N
  177292. 2/28/96V
  177293. E. J. COREY, A. K. LONG, T.W. GREENE AND J. W. MILLER, J. ORG. CHEM., 50, 1920 (1985). COMPUTER ASSISTED ANALYSIS. SELECTION OF PROTECTIVE GROUPS FOR MULTISTEP ORGANIC SYNTHESES. A REVIEW.a
  177294. GABRIEL WEATHERHEAD
  177295. 12175
  177296. 13184N
  177297. 2/28/96
  177298. YU. I. GEVAZA AND V.I. STANINETS, CHEM. HETEROCYCL. COMPDS., 359 (1985). ELECTROPHILIC HETEROCYCLIZATION OF UNSATURATED AMINO COMPOUNDS IN THE SYNTHESIS OF NITROGEN CONTAINING HETEROCYCLES. A REVIEW.a
  177299. GABRIEL WEATHERHEAD
  177300. 12176
  177301. 13185N
  177302. 2/28/96V
  177303. W.N. SPECKAMP AND H. HIEMSTRA, TETRAHEDRON, 41, 4367 (1985). INTRAMOLECULAR REACTIONS OF N ACYLIMINIUM INTERMEDIATES. A REVIEW.a
  177304. GABRIEL WEATHERHEAD
  177305. 12177
  177306. 13186N
  177307. 2/28/96VhF.D. POPP AND B.C. UFF, HETEROCYCLES, 23, 731 (1985). RING ANNELATIONS VIA REISSERT COMPOUNDS. A REVIEW.a
  177308. GABRIEL WEATHERHEAD
  177309. 12178
  177310. 13187N
  177311. 2/28/96V
  177312. E.R. STANOEVA AND M.A. KHAIMOVA, CHEM. HETEROCYCL. COMPDS., 20, 1305 (1984). HOMOPHTHALIC ANHYDRIDES AND THEIR APPLICATION TO THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. A REVIEW.a
  177313. GABRIEL WEATHERHEAD
  177314. 12179
  177315. 13188N
  177316. 2/28/96V
  177317. V.L. RUSINOV, A.YU. PETROV AND O.N. CHUPAKHIN, CHEM. HETEROCYCL. COMPOUNDS, 113 (1985). NITROAZINES. METHODS OF SYNTHESIS. A REVIEW.
  177318. GABRIEL WEATHERHEAD
  177319. 12180
  177320. 13189N
  177321. 2/28/96V
  177322. A.V. EREMEEV AND R.S. EL'KINSONM, CHEM. HETEROCYCLIC COMPDS., 20, 579 (1984). ADDITION REACTIONS IN THE 1 AZIRINE SERIES. A REVIEW.a
  177323. GABRIEL WEATHERHEAD
  177324. 12181
  177325. 13190N
  177326. 2/28/96V
  177327. J. LIEBSCHER AND H. HARTMANN, HETEROCYCLES, 23, 997 (1985). 3,5 DIARYL 1,2,4 DITHIAZOLIUM SALTS AS SYNTHONS FOR OPEN CHAINED AND HETEROCYCLIC COMPOUNDS. A REVIEW.a
  177328. GABRIEL WEATHERHEAD
  177329. 12182
  177330. 13191N
  177331. 2/28/96VZW. SLIWA AND A. THOMAS, HETEROCYCLES, 23, 399 (1985). THE CHEMISTRY OF FUROXANS. A REVIEW.a
  177332. GABRIEL WEATHERHEAD
  177333. 12183
  177334. 13192N
  177335. 2/28/96VdV.G. ANDRIANOV AND A.V. EREMEEV, CHEM. HETEROCYCL. COMPDS., 20, 937 (1984). AMINOFURAZANS. A REVIEW.a
  177336. GABRIEL WEATHERHEAD
  177337. 12184
  177338. 13193N
  177339. 2/28/96V
  177340. M. REUMAN AND A.I. MEYERS, TETRAHEDRON, 41, 837 (1985). THE SYNTHETIC UTILITY OF OXAZOLINES IN AROMATIC SUBSTITUTION. A REVIEW.a
  177341. GABRIEL WEATHERHEAD
  177342. 12185
  177343. 13194N
  177344. 2/28/96
  177345. Y. KURASAWA AND A. TAKADA, HETEROCYCLES, 23(8), 2083 (1985). RECENT PROGRESS IN THE QUINOXALINE I CHEMISTRY: UTILITY OF 3 ALKOXYCARBONYL METHYLENE 2 OXO 1,2,3,4 TETRAHYDROQUINOXALINES AS STARTING MATERIALS. A REVIEW.a
  177346. GABRIEL WEATHERHEAD
  177347. 12186
  177348. 13195N
  177349. 2/28/96VdH.C. VAN DER PLAS, TETRAHEDRON, 41, 237 (1985). RING DEGENERATE TRANSFORMATIONS OF AZINES. A REVIEW.a
  177350. GABRIEL WEATHERHEAD
  177351. 12187
  177352. 13196N
  177353. 2/28/96V}N.R. EL RAYYES AND N.A. AT AWADI, SYNTHESIS, IL 1028 (1985). SYNTHESIS OF 2 PYRAZOLINES AND 3,5 PYRAZOLIDINEDIONES. A REVIEW.a
  177354. GABRIEL WEATHERHEAD
  177355. 12188
  177356. 13197N
  177357. 2/28/96V
  177358. M H. ELNAGDI, G.E.H. ELGEMIE AND F.A. ABD ELAAL, HETEROCYCLES, 23, 3121 (1985). RECENT DEVELOPMENTS IN THE SYNTHESIS OF PYRAZOLE DERIVATIVES. A REVIEW.a
  177359. GABRIEL WEATHERHEAD
  177360. 12189
  177361. 13198N
  177362. 2/28/96VrB. IDDON, HETEROCYCLES, 23, 417 (1985). METALLATION AND METAL HALOGEN EXCHANGE REACTIONS OF IMIDAZOLES.' A REVIEW.a
  177363. GABRIEL WEATHERHEAD
  177364. 12190
  177365. 13199N
  177366. 2/28/96V
  177367. M.R. EUERBY, R.D. WAIGH, I.H. HILLIER AND J.P. HUKE, J. CHEM. SOC., PERKIN II, 1151 (1985). A THEORETICAL STUDY OF THE SITE OF ACTIVATING METHYLTHIO AND METHOXY GROUPS IN THE SYNTHESIS OF ISOQUINOLINES. A REVIEW.a
  177368. GABRIEL WEATHERHEAD
  177369. 12191
  177370. 13200N
  177371. 2/28/96V
  177372. W. SLIWA, G. MATUSIAK AND A. POSTAWKA, HETEROCYCLES, 23, 1513 (1985). THE CHEMISTRY OF N SUBSTITUTED PYRIDINIUM SALTS. A REVIEW.a
  177373. GABRIEL WEATHERHEAD
  177374. 12192
  177375. 13201N
  177376. 2/28/96V
  177377. H. BONNEMANN AND W. BRIJOUX, BULL. SOC. CHIM. BELG., 94, 635 (1985). ORGANOCOBALT COMPOUNDS IN THE SYNTHESIS OF PYRIDINES. A REVIEW.a
  177378. GABRIEL WEATHERHEAD
  177379. 12193
  177380. 13202N
  177381. 2/28/96V
  177382. T.D. BAILEY, G.L. GOE AND E.F.V. SCRIVEN, CHEM. HETEROCYCL. COMPD., 14, (PT.5), 1 (1984). SYNTHETIC AND NATURAL SOURCES OF THE PYRIDINE RING. A REVIEW.a
  177383. GABRIEL WEATHERHEAD
  177384. 12194
  177385. 13203N
  177386. 2/28/96
  177387. VtK.L. BHAT, S.Y. CHEN AND M.M. JOULLIE, HETEROCYCLES, 23, 691 (1985). D RIBONOLACTONE IN ORGANIC SYNTHESIS. A REVIEW.a
  177388. GABRIEL WEATHERHEAD
  177389. 12195
  177390. 13204N
  177391. 2/28/96V
  177392. H.M.R. HOFFMAN AND J. RABE, ANGEW. CHEM., INT. ED. ENGL., 24, 94 (1985). SYNTHESIS AND BIOLOGICAL ACTIVITY OF ALPHA METHYLENE GAMMA BUTYROLACTONES. A REVIEW.a
  177393. GABRIEL WEATHERHEAD
  177394. 12196
  177395. 13205N
  177396. 2/28/96V
  177397. M. HATANAKA, H. NITTA AND T. ISHIMARU, MEM. INST. SCI. IND. RES., OSAKA UNIV., 42, 41 52 (1985); CHEM. ABSTR., 103, 87674 (1985). SYNTHESIS OF NEW BETA LACTAM ANTIBIOTICS. A REVIEW.a
  177398. GABRIEL WEATHERHEAD
  177399. 12197
  177400. 13206N
  177401. 2/28/96V
  177402. W. DURCKHEIMER, J. BLUMBACH, R. LATTRELL AND K.H. SCHEUNEMANN, ANGEW. CHEM., INT. ED. ENGL., 24(3), 180 (1985). RECENT DEVELOPMENTS IN THE FIELD OF BETA LACTAM ANTIBIOTICS. A REVIEW.a
  177403. GABRIEL WEATHERHEAD
  177404. 12198
  177405. 13207N
  177406. 2/28/96
  177407. A.G. BROWN AND S.M. ROBERTS, ROYAL SOCIETY OF CHEMISTRY, 1984. RECENT ADVANCES IN THE CHEMISTRY OF BETA LACTAM ANTIBIOTICS. A REVIEW.a
  177408. GABRIEL WEATHERHEAD
  177409. 12199
  177410. 13208N
  177411. 2/28/96VnS. MICKEL, ALDRICHIMICA ACTA, 18, 95 (1985). 4 ACETOXY 2 AZETIDINONE: A USEFUL HETEROCYCLIC SYNTHON. A REVIEW.a
  177412. GABRIEL WEATHERHEAD
  177413. 12200
  177414. 13209N
  177415. 2/28/96V
  177416. G.W. GRIBBLE AND M.G. SAULNIER, HETEROCYCLES, 23, 1277 (1985). SYNTHESES OF ELLIPTICINE AND RELATED PYRIDOCARBAZOLE ALKALOIDS. A REVIEW.a
  177417. GABRIEL WEATHERHEAD
  177418. 12201
  177419. 13210N
  177420. 2/28/96V}E. AKGUN AND H. PINDUR, J. HETEROCYCLIC CHEM., 22; 585 (1985). CHEMICAL PROPERTIES AND SYNTHESIS OF 3 VINYLINDOLES. A REVIEW.a
  177421. GABRIEL WEATHERHEAD
  177422. 12202
  177423. 13211N
  177424. 2/28/96VhK.C. JOSHI, R. JAIN AND P. CHAND, HETEROCYCLES, 23, 957 (1985). INDOLES WITH A C 3 SPIRO ATOM. A REVIEW.a
  177425. GABRIEL WEATHERHEAD
  177426. 12203
  177427. 13212N
  177428. 2/28/96
  177429. R.A.W. JOHNSTONE, A.H. WILBY AND I.D. ENTWHISTLE, CHEM. REV.. 85, 129 (1985). HETEROGENEOUS CATALYTIC TRANSFER HYDROGENATION AND ITS RELATION TO OTHER METHODS FOR REDUCTION OF ORGANIC COMPOUNDS. A REVIEW.a
  177430. GABRIEL WEATHERHEAD
  177431. 12204
  177432. 13213N
  177433. 2/28/96V
  177434. O. STROUF, B. CASENSKY AND V. KUBANEK, 
  177435. SODIUM DIHYDRO BIS(2 METHOXYETHOXOYALUMINATE (SDMA). A VERSATILE ORGANOMETALLIC HYDRIDE. , ELSEVIER, AMSTERDAM, 1985. A REVIEW.a
  177436. GABRIEL WEATHERHEAD
  177437. 12205
  177438. 13214N
  177439. 2/28/96V
  177440. A. CLERICI AND O. PORTA, CHIM. IND. (MILAN), 67, 187 (1985). REDUCTIVE REACTIONS OF CARBONYL COMPOUNDS PROMOTED BY AQUEOUS TITANIUM TRICHLORIDE. NOVEL METHOD FOR THE SYNTHESIS OF SYMMETRICAL AND UNSYMMETRICAL PINACOLS. A REVIEW.a
  177441. GABRIEL WEATHERHEAD
  177442. 12206
  177443. 13215N
  177444. 2/28/96V
  177445. G.W. GRIBBLE AND C.F. NUTAITIS, ORG. PREP. PROC. INT., 17, 317 (1985). SODIUM BOROHYDRIDE IN CARBOXYLIC ACID MEDIA. A REVIEW OF THE SYNTHETIC UTILITY OF ACYLOXYBOROHYDRIDES. A REVIEW.a
  177446. GABRIEL WEATHERHEAD
  177447. 12207
  177448. 13216N
  177449. 2/28/96V
  177450. K.M. DEAR, CHIM. IND. (MILAN), 67, 39 (1985). PERACETIC ACID IN ORGANIC SYNTHESIS. P.N. RYLANDER, HYDROGENATION METHODS, ACADEMIC, LONDON, 1985. A DETAILED ACCOUNT, WITH EXPERIMENTAL, OF IMPORTANT SYNTHETIC METHODS IS GIVEN. A REVIEW.a
  177451. GABRIEL WEATHERHEAD
  177452. 12208
  177453. 13217N
  177454. 2/28/96VqS. TORII, ELECTROORGANIC SYNTHESIS. METHODS AND APPLICATIONS. PART I: OXIDATIONS , VCH, WEINHEIM, 1985. A REVIEW.a
  177455. GABRIEL WEATHERHEAD
  177456. 12209
  177457. 13218N
  177458. 2/28/96V
  177459. A. H. HAINES, METHODS FOR THE OXIDATION OF ORGANIC COMPOUNDS: ALKANES, ALKENES, ALKYNES AND ARENES , ACADEMIC, LONDON, 1985. A REVIEW.a
  177460. GABRIEL WEATHERHEAD
  177461. 12210
  177462. 13219N
  177463. 2/28/96V
  177464. K. INOUE, T. MATSUURA AND 1. SAITO, TETRAHEDRON, 41, 2177 (1985). RECENT ASPECTS OF SINGLET OXYGEN CHEMISTRY OF PHOTOOXIDATION. (SYMPOSIUM IN PRINT) A REVIEW.a
  177465. GABRIEL WEATHERHEAD
  177466. 12211
  177467. 13220N
  177468. 2/28/96
  177469. A. CORNELIS AND P. LASZLO, SYNTHESIS, 909 (1985). CLAY SUPPORTED COPPER(II) AND IRON(III) NITRATES: NOVEL MULTIPURPOSE REAGENTS FOR ORGANIC SYNTHESIS. A REVIEW.a
  177470. GABRIEL WEATHERHEAD
  177471. 12212
  177472. 13221N
  177473. 2/28/96VhJ. HALPERN. ANGEW. CHEM. INT. ED. ENGL. 24, 274 (1985). OXIDATION OF ORGANOMETALLIC COMPOUNDS. A REVIEW.a
  177474. GABRIEL WEATHERHEAD
  177475. 12213
  177476. 13222N
  177477. 2/28/96VhR. SHELDON, BULL. SOC. CHEM. BELG., 94, 651 (1985). CATALYTIC OXIDATIONS IN ORGANIC SYNTHESIS. A REVIEW.a
  177478. GABRIEL WEATHERHEAD
  177479. 12214
  177480. 13223N
  177481. 2/28/96V
  177482. L.G. LEE AND G. M. WHITESIDES, J. AM. CHEM. SOC., 107, 6999 (1985). ENZYME CATALYZED ORGANIC SYNTHESIS A COMPARISON OF STRATEGIES FOR TN SITU REGENERATION OF NAD FROM NADH. A REVIEW.a
  177483. GABRIEL WEATHERHEAD
  177484. 12215
  177485. 13224N
  177486. 2/28/96V
  177487. N. S. ENIKOLPYAN, RUSS. CHEM. REV. 54, 215 (1985). CATALYSIS BY METALLOPORPHYRINS OF REACTIONS INVOLVING OXIDATION BY MOLECULAR OXYGEN CONTAINING COMPOUNDS. A REVIEW.a
  177488. GABRIEL WEATHERHEAD
  177489. 12216
  177490. 13225N
  177491. 2/28/96V
  177492. J.T. GROVES AND W.J. KRUPER, JR , ISR. J. CHEM., 25, 148 (1985). METALLOPORPHYRINS IN OXIDATIVE CATALYSIS. OXYGEN TRANSFER REACTIONS OF OXOCHROMIUMPORPHYRINS. A REVIEW.a
  177493. GABRIEL WEATHERHEAD
  177494. 12217
  177495. 13226N
  177496. 2/28/96V
  177497. S. COLONNA, S. BANFI AND A. PAPAGNI, GAZZ. CHIM. ITAL., 115. 81 (1985). REVIEW; CATALYTTC ASYMETRIC EPOXIDATION IN THE PRESENCE OF CYCLODEXTRINS.
  177498.  A REVIEW.a
  177499. GABRIEL WEATHERHEAD
  177500. 12218
  177501. 13227N
  177502. 2/28/96V
  177503. H.D. GESSER, N. R. HUNTER AND C.B. PRAKASH, CHEM, REV., 85, 235 (1985). THE DIRECT CONVERSION OF METHANE TO METHANOL BY CONTROLLED OXIDATION. A REVIEW.a
  177504. GABRIEL WEATHERHEAD
  177505. 12219
  177506. 13228N
  177507. 2/28/96
  177508. J. ORGANOMETAL. CHEM., 283 (1985). ANNUAL SURVEYS: TRANSITION METALS IN ORGANIC SYNTHESIS ('83).4 TRANSITION METALS IN ORGANIC SYNTHESIS: HYDROFORMYLATION, REDUCTION AND OXIDATION ('83). COMPLEXES CONTAINING HETERONUCLEAR METAL METAL BONDS ('82 3). IRON ('82). A REVIEW.
  177509. GABRIEL WEATHERHEAD
  177510. 12220
  177511. 13229N
  177512. 2/28/96V_J. ORGANOMETAL. CHEM., 285 (1985). ORGANOMETALLICS IN ORGANIC SYNTHESIS. (46 PAPERS). A REVIEW.a
  177513. GABRIEL WEATHERHEAD
  177514. 12221
  177515. 13230N
  177516. 2/28/96V|PURE APPL. CHEM., 57 (12) (1985). REVIEWS: ORGANOMETALLIC CHEMISTRY DIRECTED TOWARD ORGANIC SYNTHESIS (20 PAPERS). A REVIEW.a
  177517. GABRIEL WEATHERHEAD
  177518. 12222
  177519. 13231N
  177520. 2/28/96V
  177521. TETRAHEDRON, 41 (24) (1985). REVIEWS: APPLICATION OF NEWER ORGANOMETALLIC REAGENTS TO THE TOTAL SYNTHESIS OF NATURAL PRODUCTS. (SYMPOSIUM IN PRINT   18 PAPERS) A REVIEW.a
  177522. GABRIEL WEATHERHEAD
  177523. 12223
  177524. 13232N
  177525. 2/28/96V
  177526. E. I. NEGISHI AND T. TAKAHASHI, ALDRICHIMICA ACTA, 18, 31 (1985). ORGANOZIRCONIUM COMPOUNDS AS NEW REAGENTS AND INTERMEDIATES. A REVIEW.a
  177527. GABRIEL WEATHERHEAD
  177528. 12224
  177529. 13233N
  177530. 2/28/96VjL. ENGMAN, ACC. CHEM. RES., 18, 274 (1985). SYNTHETIC APPLICATIONS OF ORGANOTELLURIUM CHEMISTRY. A REVIEW.a
  177531. GABRIEL WEATHERHEAD
  177532. 12225
  177533. 13234N
  177534. 2/28/96V~D. C. BILLINGTON, CHEM. SOC. REV., 14. 93 (1985). PI ALLYLNICKEL HALIDES AS SELECTIVE REAGENTS IN ORGANIC SYNTHESIS. A REVIEW.a
  177535. GABRIEL WEATHERHEAD
  177536. 12226
  177537. 13235N
  177538. 2/28/96VdP. W. JOLLY, ANGEW. CHEM., INT. ED. ENGL., 24, 283 (1985). ETA 3 ALLYLPALLADIUM COMPOUNDS. A REVIEW.a
  177539. GABRIEL WEATHERHEAD
  177540. 12227
  177541. 13236N
  177542. 2/28/96V^A. D. RYABOV, SYNTHESIS, 233 (1985). CYCLOPALLADATED COMPLEXES IN ORGANIC SYNTHESIS. A REVIEW.a
  177543. GABRIEL WEATHERHEAD
  177544. 12228
  177545. 13237N
  177546. 2/28/96VpA. D. RYABOV, RUSS. CHEM. REV., 54, 153 (1985). APPLICATION OF CYCLOPALLADIZED COMPOUNDS IN SYNTHESIS. A REVIEW.a
  177547. GABRIEL WEATHERHEAD
  177548. 12229
  177549. 13238N
  177550. 2/28/96V
  177551. H. YASUDA, K. TATSUMI AND A. NAKAMURA, ACC. CHEM. RES., 18, 120 (1985). UNIQUE CHEMICAL BEHAVIOR AND BONDING OF EARLY TRANSITION METAL DIENE COMPLEXES. A REVIEW.a
  177552. GABRIEL WEATHERHEAD
  177553. 12230
  177554. 13239N
  177555. 2/28/96
  177556. K. JONAS, ANGEW. CHEM., INT. ED. ENGL., 24, 295 (1985). REACTIVE ORGANOMETALLIC COMPOUNDS OBTAINED FROM METALLOCENES AND RELATED COMPOUNDS AND THEIR SYNTHETIC APPLICATIONS. A REVIEW.a
  177557. GABRIEL WEATHERHEAD
  177558. 12231
  177559. 13240N
  177560. 2/28/96V
  177561. B. BOGDANOVIC, ANGEW. CHEM., INT. ED. ENGL.. 24, 262 CATALYTIC SYNTHESIS OF ORGANOLITHIUM AND ORGANOMAGNESIUM COMPOUNDS AND OF LITHIUM AND MAGNESIUM HYDRIDES   APPLICATIONS IN ORGANIC SYNTHESIS AND HYDROGEN STORAGE. A REVIEW.a
  177562. GABRIEL WEATHERHEAD
  177563. 12232
  177564. 13241N
  177565. 2/28/96V
  177566. K. MARUOKA AND H. YAMAMOTO, ANGEW. CHEM., INT. ED. ENGL., 24, 668 (1985). SELECTIVE REACTIONS USING ORGANOALUMINUM REAGENTS. A REVIEW.a
  177567. GABRIEL WEATHERHEAD
  177568. 12233
  177569. 13242N
  177570. 2/28/96VnT. L. HO, TETRAHEDRON, 41, 3 (1985). CHEMOSELECTIVITY OF ORGANOMETALLIC REACTIONS. A HSAB APPRAISAL. A REVIEW.a
  177571. GABRIEL WEATHERHEAD
  177572. 12234
  177573. 13243N
  177574. 2/28/96
  177575. ?V{D. S. MATTESON ET AL., J. ORGANOMETAL. CHEM., 281, 15 (1985). 
  177576. DIRECTED ASYMMETRIC SYNTHESIS WITH BORONIC ESTERS. A REVIEW.a
  177577. GABRIEL WEATHERHEAD
  177578. 12235
  177579. 13244N
  177580. 2/28/96V_WIDMER, PURE APPL. CHEM., 57, 741 (1985). SYNTHETIC ADVANCES IN THE CAROTENOID FIELD. A REVIEW.a
  177581. GABRIEL WEATHERHEAD
  177582. 12236
  177583. 13245N
  177584. 2/28/96VrH. PFANDER, PURE APPL. CHEM., 57, 735 (1985). ADVANCES IN THE SYNTHESIS OF OPTICALLY ACTIVE CAROTENOIDS. A REVIEW.a
  177585. GABRIEL WEATHERHEAD
  177586. 12237
  177587. 13246N
  177588. 2/28/96VePARDO AND M. SANTELLI, BULL. SOC. CHIM. FR., 98 (1985). SYNTHESIS OF VITAMIN D METABOLITES. A REVIEW.a
  177589. GABRIEL WEATHERHEAD
  177590. 12238
  177591. 13247N
  177592. 2/28/96V_J. FINK AND M. REGITZ, SYNTHESIS, 569 (1985). ELECTROPHILIC DIAZOALKANE SUBSTITUTION. A REVIEW.a
  177593. GABRIEL WEATHERHEAD
  177594. 12239
  177595. 13248N
  177596. 2/28/96
  177597. M YANDEWALLE AND P. DECLERCQ, TETRAHEDRON, 41, 1767 (1985) TOTAL SYNTHESIS OF POLYCARBOCYCLIC SESQUITERPENES. A SURVEY OF NOVEL METHODS AND REACTIONS. A REVIEW.a
  177598. GABRIEL WEATHERHEAD
  177599. 12240
  177600. 13249N
  177601. 2/28/96V
  177602. I. PATERSON AND M. M. MANSURI, TETRAHEDRON, 41, 3569 (1985). RECENT DEVELOPMENTS IN THE TOTAL SYNTHESIS OF MACROLIDE ANTIBIOTICS. A REVIEW.a
  177603. GABRIEL WEATHERHEAD
  177604. 12241
  177605. 13250N
  177606. 2/28/96VvJ. ROKACH AND J. ADAMS, ACC. CHEM. RES., 18. 87 (1985). SYNTHESIS OF LEUKOTRIENES AND LIPOXYGENASE PRODUCTS. A REVIEW.a
  177607. GABRIEL WEATHERHEAD
  177608. 12242
  177609. 13251N
  177610. 2/28/96V
  177611. N. S. ZEFIROV AND A. S. KOZ'MIN, ACC. CHEM. RES., 8, 154 (1985). COMPETITIVE BINDING OF NUCLEOFUGAL ANIONS IN CARBOCATIONIC LIKE PROCESSES. A REVIEW.a
  177612. GABRIEL WEATHERHEAD
  177613. 12243
  177614. 13252N
  177615. 2/28/96VYB. M. TROST, SCIENCE, 2Z7, 908 (1985). SCULPTING HORIZONS IN ORGANIC CHEMISTRY. A REVIEW.a
  177616. GABRIEL WEATHERHEAD
  177617. 12244
  177618. 13253N
  177619. 2/28/96
  177620. IVzR. SCHEFFOLD, CHIMIA, 39, 203 (1985). VITAMIN BL2. CATALYST FOR CC BOND FORMATION IN ORGANIC CHEMICAL SYNTHESIS. A REVIEW.a
  177621. GABRIEL WEATHERHEAD
  177622. 12245
  177623. 13254N
  177624. 2/28/96VlJ. M. LEHN, SCIENCE, Z27, 849 (1985). SUPRAMOLECULAR CHEMISTRY: RECEPTORS, CATALYSTS AND CARRIERS. A REVIEW.a
  177625. GABRIEL WEATHERHEAD
  177626. 12246
  177627. 13255N
  177628. 2/28/96VeJ. K. WHITESELL, ACC. CHEM. RES., 18, 280 (1985). NEW PERSPECTIVES IN ASYMMETRIC INDUCTION. A REVIEW.a
  177629. GABRIEL WEATHERHEAD
  177630. 12247
  177631. 13256N
  177632. 2/28/96V
  177633. S. MASAMUNE ET AL., ANGEW. CHEM., INT. ED. ENGL., 24, 1 (1985). DOUBLE ASYMMETRIC SYNTHESIS AND A NEW STRATEGY FOR STEREOCHEMICAL CONTROL IN ORGANIC SYNTHESIS. A REVIEW.a
  177634. GABRIEL WEATHERHEAD
  177635. 12248
  177636. 13257N
  177637. 2/28/96V
  177638. T. MUKAIYAMA AND M. ASAMI, TOP. CURR. CHEM., 127, 133 (1985). CHIRAL PYRROLIDINE DIAMINES AS EFFICIENT LIGANDS IN ASYMMETRIC SYNTHESIS. A REVIEW.a
  177639. GABRIEL WEATHERHEAD
  177640. 12249
  177641. 13258N
  177642. 2/28/96
  177643. TETRAHEDRON, 41 (19) (1985). REVIEWS: SELECTIVITY AND SYNTHETIC APPLICATIONS OF RADICAL REACTIONS. (SYMPOSIUM IN PRINT   29 PAPERS) A REVIEW.a
  177644. GABRIEL WEATHERHEAD
  177645. 12250
  177646. 13259N
  177647. 2/28/96VTZ. V. TODRES, TETRAHEDRON, 41, 2771 (1985). ION RADICAL ORGANIC REACTIONS. A REVIEW.a
  177648. GABRIEL WEATHERHEAD
  177649. 12251
  177650. 13260N
  177651. 2/28/96VVH. G. VIEHE ET AL., ACC. CHEM. RES., 18, 148 (1985). THE CAPTODATIVE EFFECT. A REVIEW.a
  177652. GABRIEL WEATHERHEAD
  177653. 12252
  177654. 13261N
  177655. 2/28/96VmR. J. K. TAYLOR, SYNTHESIS, 364 (1985). ORGANOCOPPER CONJUGATE ADDITION ENOLATE TRAPPING REACTIONS. A REVIEW.a
  177656. GABRIEL WEATHERHEAD
  177657. 12253
  177658. 13262N
  177659. 2/28/96V
  177660. A. YOSHIKOSHI AND M. MIYASHITA, ACC. CHEM. RES., 8, 284 (1985) . OXOALKYLATION OF CARBONYL COMDOUNDS WITH CONJUGATED NITRO OLEFINS. A REVIEW.a
  177661. GABRIEL WEATHERHEAD
  177662. 12254
  177663. 13263N
  177664. 2/28/96
  177665. C. BOTTEGHI AND F. SOCCOLINI, SYNTHESIS, 592 (1985). MALONALDEHYDE, SUCCINALDEHYDE AND GLUTARALDEHYDE MONOACETALS: SYNTHESIS AND APPLICATIONS. A REVIEW.a
  177666. GABRIEL WEATHERHEAD
  177667. 12255
  177668. 13264N
  177669. 2/28/96V^R. ANDERSON, SYNTHESIS, 717 (1985). SYNTHETIC APPLICATIONS OF CHLOROTRIMETHYLSILANE. A REVIEW.a
  177670. GABRIEL WEATHERHEAD
  177671. 12256
  177672. 13265N
  177673. 2/28/96VyS. V. LEY, CHEM. IND. (LONDON), 101 (1985). ORGANOSELENIUM MEDIATED CYCLISATION REACTIONS IN ORGANIC SYNTHESIS. A REVIEW.a
  177674. GABRIEL WEATHERHEAD
  177675. 12257
  177676. 13266N
  177677. 2/28/96V~TETRAHEDRON, 41 (21 ) (1985) . REVIEWS: RECENT ASPECTS OF ORGANOSELENIUM CHEMISTRY. (SYMPOSIUM IN PRINT   17 PAPERS) A REVIEW.a
  177678. GABRIEL WEATHERHEAD
  177679. 12258
  177680. 13267N
  177681. 2/28/96V
  177682. A. I. MEYERS, ALDRICHIMICA ACTA, 18, 59 (1985). FORMAMIDINES AS PRECURSORS TO ALPHA AMINO CARBANIONS AND THEIR APPLICATION TO ASYMMETRIC C C BOND FORMING REACTIONS. A REVIEW.a
  177683. GABRIEL WEATHERHEAD
  177684. 12259
  177685. 13268N
  177686. 2/28/96
  177687. XVqI. KUWAJIMA AND E. NAKAMURA, ACC. CHEM. RES., 18, 181 (1985). REACTIVE ENOLATES FROM ENOL SILYL ETHERS. A REVIEW.a
  177688. GABRIEL WEATHERHEAD
  177689. 12260
  177690. 13269N
  177691. 2/28/96VkH. C. BROWN AND B. SINGARAM, CHEMTECH, 572 (1985). AN ASYMMETRIC SYNTHESIS THAT'S REALLY GENERAL. A REVIEW.a
  177692. GABRIEL WEATHERHEAD
  177693. 12261
  177694. 13270N
  177695. 2/28/96V
  177696. E. I. NEGISHI AND M. J. IDACAVAGE, ORG. REACTIONS, 33, 1 (1985) FORMATION OF CARBON CARBON AND CARBON HETEROATOM BONDS VIA ORGANOBORANES AND ORGANOBORATES.
  177697.  A REVIEW.a
  177698. GABRIEL WEATHERHEAD
  177699. 12262
  177700. 13271N
  177701. 2/28/96VpN. BALASUBRAMANIAN, ORG. PREP. PROCED. INT., 17, 23 (1985). RECENT SYNTHETIC APPLICATIONS OF NITRONES. A REVIEW.a
  177702. GABRIEL WEATHERHEAD
  177703. 12263
  177704. 13272N
  177705. 2/28/96V
  177706. TETRAHEDRON, 41 (17) (1985). REVIEWS: SYNTHETIC APPLICATIONS OF DIPOLAR CYCLOADDITION REACTIONS. (SYMPOSIUM IN PRINT   11 PAPERS) A REVIEW.a
  177707. GABRIEL WEATHERHEAD
  177708. 12264
  177709. 13273N
  177710. 2/28/96
  177711. ]VeD. MODERHACK, SYNTHESIS, 1083 (1985). FOUR MEMBERED RINGS FROM ISOCYANIDES RECENT ADVANCES. A REVIEW.a
  177712. GABRIEL WEATHERHEAD
  177713. 12265
  177714. 13274N
  177715. 2/28/96VtS. L. SCHREIBER, SCIENCE, 227, 857 (1985). [2+2] PHOTOCYCLOADDITIONS IN THE SYNTHESIS OF CHIRAL MOLECULES. A REVIEW.a
  177716. GABRIEL WEATHERHEAD
  177717. 12266
  177718. 13275N
  177719. 2/28/96V
  177720. S. M. WEINREB, ACC. CHEM. RES., 18, 16 (1985). ALKALOID TOTAL SYNTHESIS BY INTRAMOLECULAR IMINO DIELS ALDER CYCLOADDITIONS. A REVIEW.a
  177721. GABRIEL WEATHERHEAD
  177722. 12267
  177723. 13276N
  177724. 2/28/96VnC. J. M. STIRLING, TETRAHEDRON, 41. 1613 (1985). EVALUATION OF THE EFFECT OF STRAIN UPON REACTIVITY. A REVIEW.a
  177725. GABRIEL WEATHERHEAD
  177726. 12268
  177727. 13277N
  177728. 2/28/96V
  177729. E. VILSMAIER, BULL. SOC. CHIM. BELG., 94. 521 (1985). DIACYLMETHYLENE CYCLOPROPANES AS INTERMEDIATES IN A CYCLOPROPANE SUBSTITUTION IN AMINOCYCLOPROPANES. A REVIEW.a
  177730. GABRIEL WEATHERHEAD
  177731. 12269
  177732. 13278N
  177733. 2/28/96
  177734. B. FRASER REID, ACC. CHEM. RES., 18, 347 (1985). SOME PROGENY OF 2,3 UNSATURATED SUGARS THEY LITTLE RESEMBLE GRANDFATHER GLUCOSE: TEN YEARS LATER.
  177735.  A REVIEW.a
  177736. GABRIEL WEATHERHEAD
  177737. 12270
  177738. 13279N
  177739. 2/28/96V
  177740. H. M. R. HOFFMANN AND J. RABE, ANGEW. CHEM., INT. ED. ENGL., 24, 94 (1985). SYNTHESIS AND BIOLOGICAL ACTIVITY OF ALPHA METHYLENE GAMMA BUTYROLACTONES. A REVIEW.a
  177741. GABRIEL WEATHERHEAD
  177742. 12271
  177743. 13280N
  177744. 2/28/96V
  177745. Z. RAPPOPORT, REC. TRAV. CHIM., 104. 309 (1985). THE RICH MECHANISTIC WORLD OF NUCLEOPHILIC VINYLIC (SNV) SUBSTITUTION. A REVIEW.a
  177746. GABRIEL WEATHERHEAD
  177747. 12272
  177748. 13281N
  177749. 2/28/96V_M. JULIA, PURE APPL. CHEM., 57, 763 (1985). RECENT ADVANCES IN DOUBLE BOND FORMATION. A REVIEW.a
  177750. GABRIEL WEATHERHEAD
  177751. 12273
  177752. 13282N
  177753. 2/28/96VsB. E. MARYANOFF ET AL., J. AM. CHEM. SOC., 107, 217, 1068 (1985). STEREOCHEMISTRY OF THE WITTIG REACTION. A REVIEW.a
  177754. GABRIEL WEATHERHEAD
  177755. 12274
  177756. 13283N
  177757. 2/28/96
  177758. gV_J. LUGTENBURG, PURE APPL. CHEM 57, 753 (1985). THE SYNTHESIS OF L3C LABELED RETINALS. A REVIEW.a
  177759. GABRIEL WEATHERHEAD
  177760. 12275
  177761. 13284N
  177762. 2/28/96V
  177763. BULL. SOC. CHIM. BELG. 99(9), 1990 ALPHA,ALPHA' OLIGOPYRIDINES   A SOURCE OF NEW MATERIALS. POTTS K. T., PP. 741 68 (36 REFERENCES). A REVIEW.a
  177764. GABRIEL WEATHERHEAD
  177765. 12276
  177766. 13285N
  177767. 2/28/96V
  177768. BULL. SOC. CHIM. BELG. 99(9), 1990 ENANTIOSELECTIVE CATALYSIS WITH METAL COMPLEXES CONTAINING HETEROCYCLIC LIGANDS. PFALTZ A., PP. 729 39 (16 REFERENCES). A REVIEW.a
  177769. GABRIEL WEATHERHEAD
  177770. 12277
  177771. 13286N
  177772. 2/28/96V
  177773. BULL. SOC. CHIM. BELG. 99(9), 1990 SYNTHESIS OF INDOLE ALKALOIDS AND RETATED MOLECULES ALONG NONBIOGENETIC ROUTES. MASSIOT G., PP. 717 28 (10 REFERENCES). A REVIEW.a
  177774. GABRIEL WEATHERHEAD
  177775. 12278
  177776. 13287N
  177777. 2/28/96V
  177778. BULL. SOC. CHIM. BELG. 99(9), 1990 SYNTHESIS AND REACTIONS OF 2H BENZIMIDAZOLE 2 SPIROCYCLOHEXANES   AN APPLICATION OF UMPOLUNG. IDDON B., PP. 673 701 (34 REFERENCES). A REVIEW.
  177779. GABRIEL WEATHERHEAD
  177780. 12279
  177781. 13288N
  177782. 2/28/96
  177783. BULL. SOC. CHIM. BELG. 99(9), 1990 FLUORINATED HETEROCYCLES   TARGETS IN THE SEARCH FOR BIOACTIVE COMPOUNDS AND TOOLS FOR THEIR PREPARATION. DIFFERDING E., FRICK W., LANG R. W., MARTIN P., SCHMIT C., VEENSTRA S., GREUTER H., PP. 647 71 (39 REFERENCES). A REVIEW.
  177784. GABRIEL WEATHERHEAD
  177785. 12280
  177786. 13289N
  177787. 2/28/96V
  177788. BULL. SOC. CHIM. BELG. 99(9), 1990 MODEL STUDIES DIRECTED TOWARDS MICROALGA POLYETHER TOXINS. ALVAREZ E., DIAZ M. T., ZURITA D., ZARRAGA M., MARTIN J. D., PP. 635 45 (23 REFERENCES). A REVIEW.a
  177789. GABRIEL WEATHERHEAD
  177790. 12281
  177791. 13290N
  177792. 2/28/96V
  177793. BULL. SOC. CHIM. BELG. 99(9), 1990 DESIGN, SYNTHESIS, AND PROPERTIES OF MACROCYCLIC RECEPTORS FOR TETRAHEDRAL SUBSTRATES. COLLET A., DUTASTA J. P., LOZACH B., PP. 617 33 (21 REFERENCES). A REVIEW.a
  177794. GABRIEL WEATHERHEAD
  177795. 12282
  177796. 13291N
  177797. 2/28/96
  177798. BULL. SOC. CHIM. BELG. 99(9), 1990 DIELS ALDER REACTION OF AZADIENES   SCOPE AND APPLICATIONS. BOGER D. L., PP. 599 615 (59 REFERENCES). A REVIEW.a
  177799. GABRIEL WEATHERHEAD
  177800. 12283
  177801. 13292N
  177802. 2/28/96V
  177803. KHIM. FARM. ZH. SSSR 24(11), 1990 IMMUNOTROPIC ACTIVITG OF AZOLE DERIVATIVES AND THEIR CONDENSED HETEROCYCLIC SYSTEMS. SIBIRYAK S. V., STROKIN Y. V., SADYKOV R. F., DIANOV V. M., PP. 19 24 (59 REFERENCES). IN RUSSIAN. A REVIEW.a
  177804. GABRIEL WEATHERHEAD
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  177806. 13293N
  177807. 2/28/96V
  177808. KHIM. FARM. ZH. SSSR 24(11), 1990 PROSTAGLANDINS AND MALIGNANT NEOPLASMS. IGNATOVICH L. G., FREIMANIS Y. F., PP. 4 10 (104 REFERENCES). IN RUSSIAN. A REVIEW.a
  177809. GABRIEL WEATHERHEAD
  177810. 12285
  177811. 13294N
  177812. 2/28/96V
  177813. KHIM. PRIR. SOEDIN. SSSR (3), 1990 ALANTOLACTONES AND ISOALANTOLACTONES. MILMAN 1. A., PP. 307  20 (148 REFERENCES). IN RUSSIAN. A REVIEW.a
  177814. GABRIEL WEATHERHEAD
  177815. 12286
  177816. 13295N
  177817. 2/28/96
  177818. PHAKMAZIE 45(12), 1990 CHEMICAL AND ENZYMATIC METHODS FOR THE SYNTHESIS OF THE PEPTIDE SWEETENING AGENT ASPARTAME. KUHL P., PP. 881 7 (174 REFERENCES). HN GERMAN. A REVIEW.a
  177819. GABRIEL WEATHERHEAD
  177820. 12287
  177821. 13296N
  177822. 2/28/96V
  177823. SYNTHESIS STUTTGART (10),1990 OXIDATION OF ALCOHOLS BY ACTIVATED DIMETHYL SULFOXIDE AND RELATED RESCTIONS   AN UPDATE. TIDWELL T. T., PP. 857 70 (148 REFERENCES). A REVIEW.a
  177824. GABRIEL WEATHERHEAD
  177825. 12288
  177826. 13297N
  177827. 2/28/96VvNEW J. CHEM. 14(10), 1990 MARINE CAROTENOIDS   SELECTED TOPICS. LIAAENJENSEN S., PP. 747 59 (91 REFERENCES). A REVIEW.a
  177828. GABRIEL WEATHERHEAD
  177829. 12289
  177830. 13298N
  177831. 2/28/96V
  177832. NEW J. CHEM. 14(10), 1990 STRUCTURE AND BIOSYNTHESIS OF CYCLOPROPANE CONTAINING STEROLS OF MARINE ORIGIN. DJERASSI C., DOSS G. A., PP. 713 9 (80 REFERENCES). A REVIEW.a
  177833. GABRIEL WEATHERHEAD
  177834. 12290
  177835. 13299N
  177836. 2/28/96
  177837. NEW J. CHEM. 14(10), 1990 RECENT DEVELOPMENTS IN RESEARCH ON METABOLITES FROM RED SEA INVERTEBRATES. KASHRNAN Y., RUDI A., HIRSH S., ISAACS S., GREEN D., BLASBERGER D., CARRNELY S., PP. 729 40 (38 REFERENCES). A REVIEW.a
  177838. GABRIEL WEATHERHEAD
  177839. 12291
  177840. 13300N
  177841. 2/28/96VsTETRAHEDRON 46(17), 1990 GLYCOSIDATION OF SIALIC ACID. OKAMOTO K., GOTO T., PP. 5835 57 (134 REFERENCES). A REVIEW.a
  177842. GABRIEL WEATHERHEAD
  177843. 12292
  177844. 13301N
  177845. 2/28/96V
  177846. KHIM. GETEROTSIKL. SOEDIN. SSSR (11), 1990 SYNTHESIS OF FURAZANS BY REARRANGEMENT OF 3 ACYL L OXA 2 AZOLE OXIMES. ANDRIANOV V. G., EREMEEV A. V., PP. 1443 59 (96 REFERENCES). IN RUSSIAN. A REVIEW.a
  177847. GABRIEL WEATHERHEAD
  177848. 12293
  177849. 13302N
  177850. 2/28/96V
  177851. Z. CHEM. 30(11), 1990 REACTIONS OF ALPHA HETEROCARBANIONS WITH SULFUR CONTAINING HETEROCUMULENES. AUGUSTIN M., DOLLING W., PP. 395 403 (129 REFERENCES). IN GERMAN. A REVIEW.a
  177852. GABRIEL WEATHERHEAD
  177853. 12294
  177854. 13303N
  177855. 2/28/96
  177856. PHYTOCHEMISTRY 30(1), 1991 ACETYLENES AND RELATED COMPOUNDS IN HELIANTHEAE. CHRISTENSEN L, P., LAM J., PP. 11 49(246 REFERENCES). A REVIEW.a
  177857. GABRIEL WEATHERHEAD
  177858. 12295
  177859. 13304N
  177860. 2/28/96VuSYNLETT. (8), 1990 THE ROLE OF METAL IN CARBENE SYNTHON INTRODUCTION. NOZAKI H., PP. 441 4 (18 REFERENCES). A REVIEW.a
  177861. GABRIEL WEATHERHEAD
  177862. 12296
  177863. 13305N
  177864. 2/28/96V
  177865. SYNLETT. (8), 1990 AN OVERVIEW OF THE TOTAL SYNTHESIS OF PYRROLIZIDINE ALKALOIDS VIA (4+1) AZIDE DIENE ANNULATION METHODOLOGY. HUDLICKY T., SEOANE G., PRICE J. D., GADAMASETTI K. G., PP. 433 40 (28 REFERENCES). A REVIEW.a
  177866. GABRIEL WEATHERHEAD
  177867. 12297
  177868. 13306N
  177869. 2/28/96V
  177870. NIPPON KAGAKU KAISHI (1), 1991  DYE RELEASERS FOR INSTANT COLOR PHOTOGRAPHY   MOLECULAR DESIGN AND SYNTHETIC DESIGN. FUJITA S., KOYARNA K., ONO S., PP. 1  12 (19 REFERENCES). IN JAPANESE. A REVIEW.a
  177871. GABRIEL WEATHERHEAD
  177872. 12298
  177873. 13307N
  177874. 2/28/96
  177875. YAKUGAKU ZASSHI J. PHARM. SOC. J. 111(1), 1991  STUDIES ON TOTAL SYNTHESES OF CYTOTOXIC CYCLIC PEPTIDES OF MARINE ORIGIN. HAMATLA Y., PP. 1 18 (55 REFERENCES). IN JAPANESE. A REVIEW.a
  177876. GABRIEL WEATHERHEAD
  177877. 12299
  177878. 13308N
  177879. 2/28/96V
  177880. TOP. CURR. CHEM. 157, 1990 CHEMICAL REACTIONS INDUCED AND PROBED BY POSITIVE MUONS. ITO Y., PP. 93 128 (73 REFERENCES). A REVIEW.a
  177881. GABRIEL WEATHERHEAD
  177882. 12300
  177883. 13309N
  177884. 2/28/96VvTOP. CURR. CHEM. 156, 1990 ELECTRON TRANSFER PROCESSES IN IMAGING. EATON D. F., PP. 199 225 (68 REFERENCES). A REVIEW.a
  177885. GABRIEL WEATHERHEAD
  177886. 12301
  177887. 13310N
  177888. 2/28/96V}TOP. CURR. CHEM. 156, 1990 PHOTOINDUCED ELECTRON TRANSFER POLYMERIZATION. TIMPE H. J., PP. 167 97 (182 REFERENCES). A REVIEW.a
  177889. GABRIEL WEATHERHEAD
  177890. 12302
  177891. 13311N
  177892. 2/28/96V
  177893. ANGEW. CHEM. INT. ED. 29(8), 1990 NONMOLECULAR METAL CHALCOGENIDE HALIDE SOLIDS AND THEIR MOLECULAR CLUSTER ANALOGS. LEE S. C., HOLM R. H., PP 840 56 (194 REFERENCES). A REVIEW.
  177894. GABRIEL WEATHERHEAD
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  177896. 13312N
  177897. 2/28/96
  177898. EORG. PREP. PROCEDURE INT. 22(4), 1990 SYNTHESIS OF ALPHA AMINOALDEHYDES AND ALPHA AMINOKETONES. FISHER L. E., MUCHOWSKI J. M., PP. 399 484 (206 REFERENCES). SYNTHESES, CONFORMATIONS AND X RAY STRUCTURE ANALYSES OF THE SACCHARIDE CHAINS FROM THE CORE REGIONS OF GLYCOPROTEINS. PAULSEN H.. PP. 823 39 (90 REFERENCCS). A REVIEW.
  177899. GABRIEL WEATHERHEAD
  177900. 12304
  177901. 13313N
  177902. 2/28/96V
  177903. KHIM. GETEROTSIKL. SOEDIN. SSSR (10), 1990 THREE MEMBERED HELEROCYCLES IN THE SYNTHESIS OF CROWN COMPOUNDS AND CRYPTANDS. VORONKOV M. G.. KNUTOV V. 1., SHEVKO O. N., PP. 1299 315 (85 REFERENCCS) IN RUSSIAN. A REVIEW.a
  177904. GABRIEL WEATHERHEAD
  177905. 12305
  177906. 13314N
  177907. 2/28/96V
  177908. TETRAHEDRON 46(16), 1990 ALPHA OXOKETENES S,S ACETAL, N,S ACETAL AND N,N ACETAL   VERSATILE INTERMEDIATES IN ORGANIC SYNTHESIS. JUNJAPPA H., LLA H., ASOKAN C. V., PP. 5423 506 (225 REFERENCES). A REVIEW.a
  177909. GABRIEL WEATHERHEAD
  177910. 12306
  177911. 13315N
  177912. 2/28/96VkTETRAHEDRON 46(15), 1990 ASYMMETRIC SYNTHESIS OF LIGNANS. WARD R. S. PP. 5029 41 (23 REFERENCES). A REVIEW.a
  177913. GABRIEL WEATHERHEAD
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  177915. 13316N
  177916. 2/28/96V
  177917. J. SYN. ORG. CHEM. JPN. 49(1), 1991  MICROBIAL CARBONYL REDUCTASES   THEIR DIVERSITY AND APPLICATION TO THE SYNTHESIS OF OPTICALLY ACTIVE ALCOHOLS. SHIMIZU S. YAMADA H., PP 52 70 (27 REFERENCES). IN JAPANESE. A REVIEW.a
  177918. GABRIEL WEATHERHEAD
  177919. 12308
  177920. 13317N
  177921. 2/28/96V
  177922. J. SYN. ORG. CHEM. JPN. 49(1), 1991 ESTER AND PEPTIDE SYNTHESIS BY PROTEASES IN ORGANIC SOLVENTS. KISE H., PP 42 51 (106 REFERENCES). IN JAPANESE. A REVIEW.a
  177923. GABRIEL WEATHERHEAD
  177924. 12309
  177925. 13318N
  177926. 2/28/96V
  177927. J. SYN. ORG. CHEM. JPN. 49(1), 1991 CHEMISTRY OF ASPARTIC ACID AND ITS APPLICATION TO DRUG SYNTHESIS. MATSUMOTO K., SEKI M., PP. 26 41 (68 REFERENCES). IN JAPANESE. A REVIEW.a
  177928. GABRIEL WEATHERHEAD
  177929. 12310
  177930. 13319N
  177931. 2/28/96
  177932. J. SYN. ORG. CHEM. JPN. 49(1), 1991 DESIGN AND SYNTHESIS OF METABOLICALLY STABLE ANALOG OF DYNORPHIN A. TACHIBANA S., YOSHINO H., PP. 16 25 (32 REFERENCES). IN JAPANESE. A REVIEW.a
  177933. GABRIEL WEATHERHEAD
  177934. 12311
  177935. 13320N
  177936. 2/28/96V
  177937. J. SYN. ORG. CHEM. JPN. 48(12), 1990 GENERATION OF REACTIVE SPECIES OF ORGANOMETALLIC COMPOUNDS AND THEIR APPLICATIONS IN ORGANIC SYNTHESIS. OTSUJI Y., PP. 2 15 (47 REFERENCES). IN JAPANESE. A REVIEW.a
  177938. GABRIEL WEATHERHEAD
  177939. 12312
  177940. 13321N
  177941. 2/28/96V
  177942. J. SYN. ORG. CHEM. JPN. 48(12), 1990 RECENT ADVANCES IN ORGANIC SYNTHESIS USING HALOBORATION REACTIONS. HARA 5., PP. 1125 37 (13 REFERENCES). IN JAPANESE. A REVIEW.a
  177943. GABRIEL WEATHERHEAD
  177944. 12313
  177945. 13322N
  177946. 2/28/96V
  177947. J. SYN. ORG. CHEM. JPN. 48(12), 1990 SYNTHESIS OF POLY(CROWN ETHER)S VIA CYCLOPOLYMERIZATION AND THEIR HOST PROPERTY. KAKUCHI T., YOKOTA K., PP. 1106 14 (29 REFERENCES). IN JAPANESE. A REVIEW.a
  177948. GABRIEL WEATHERHEAD
  177949. 12314
  177950. 13323N
  177951. 2/28/96
  177952. J. SYN. ORG. CHEM. JPN. 48(12), 1990 RECENT PROGRESS IN 1,3 POLYOL SYNTHESIS. MORI Y., PP. 1092 105 (60 REFERENCES). IN JAPANESE. A REVIEW.a
  177953. GABRIEL WEATHERHEAD
  177954. 12315
  177955. 13324N
  177956. 2/28/96V
  177957. RECENT ADVANCES IN THE SYNTHESIS OF VITAMIN D ANALOGS. ANDO K., TAKAYAMA H.. PP. 1082 91 (56 REFERENCES). IN JAPANESE. A REVIEW.a
  177958. GABRIEL WEATHERHEAD
  177959. 12316
  177960. 13325N
  177961. 2/28/96V
  177962. J. ORGANOMETAL. CHEM. 394(1 3), 1990 BIS(DIPHENYLPHOSPHINO)METHANIDE OR BIS(DIPHENYLPHOSPHINO)AMIDE AND ITS DERIVATIVES AS LIGANDS IN GOLD CHEMISTRY. LAGUNA A., LAGUNA M., PP. 743 56 (28 REFERENCES). A REVIEW.a
  177963. GABRIEL WEATHERHEAD
  177964. 12317
  177965. 13326N
  177966. 2/28/96V
  177967. J. ORGANOMETAL. CHEM. 394(1 3), 1990 THE STEREOSPECIFIC SYNTHESIS OF MONONUCLEAR AND BINUCLEAR (LIGAND BRIDGED) CARBONYL COMPLEXES OF MANGANESE. CAMEDO G. A., RIERA V., PP 275 83 (37 REFERENCES). A REVIEW.a
  177968. GABRIEL WEATHERHEAD
  177969. 12318
  177970. 13327N
  177971. 2/28/96
  177972. KHIM. FARM. ZH. SSSR 24(10), 1990 PREGNA D' PENTARANES   SYNTHESIS, MODIFCATIONS, STRUCTURE. LEVINA I. S., KARNERNITSKY A. V., PP. 31 9 (80 REFERENCES). IN RUSSIAN. A REVIEW.a
  177973. GABRIEL WEATHERHEAD
  177974. 12319
  177975. 13328N
  177976. 2/28/96V
  177977. TETRAHEDRON 46(19), 1990 APPLICATIONS OF PIG LIVER ESTERASES (PLE) IN ASYMMETRIC SYNTHESIS. ZHN L. M., TEDFORD M. C., PP. 6587 611 (76 REFERENCES). A REVIEW.a
  177978. GABRIEL WEATHERHEAD
  177979. 12320
  177980. 13329N
  177981. 2/28/96V
  177982. SYNTHESIS STUTTGART (8),1990 NEW ASPECTS OF STEREOSCLECTIVE SYNTHESTS OF 1,3 POLYOLS. OISHI T., NAKATA T., PP. 635 45 (49 REFERENCES). A REVIEW.a
  177983. GABRIEL WEATHERHEAD
  177984. 12321
  177985. 13330N
  177986. 2/28/96V
  177987. POLYHEDRON 9(23), 1990 COORDINATELY UNSATURATED TRIPALLADIUM AND TRIPLATINUM CLUSTERS   MODELS FOR REACTIONS ON METAL SURFACES. PUDDEPHATT R. J., MANOJLOVICMUIR L., MUIR K. W., PP. 2767 802 (100 REFERENCES). A REVIEW.a
  177988. GABRIEL WEATHERHEAD
  177989. 12322
  177990. 13331N
  177991. 2/28/96
  177992. POLYHEDRON 9(13), 1990 KINETICS AND MECHANISM OF CO SUBSTITUTION OF METAL CARBONYLS. BASOLO F., PP 1503 35 (157 REFERENCES). A REVIEW.a
  177993. GABRIEL WEATHERHEAD
  177994. 12323
  177995. 13332N
  177996. 2/28/96VqTETRAHEDRON 46(20), 1990 THE CHEMISTRY OF VINYL SULFONES. SIMPKINS N. S., PP. 6951 84 (132 REFERENCES). A REVIEW.a
  177997. GABRIEL WEATHERHEAD
  177998. 12324
  177999. 13333N
  178000. 2/28/96V
  178001. ANGEW. CHEM. INT. ED. 29(9), 1990 THE DIRECTED SYNTHESIS OR BIARYL COMPOUNDS   MODERN CONCEPTS AND STRATEGIES. BRINGMANN G.. WALTER R., WEIRICH R., PP. 977 91 (157 REFERENCES). A REVIEW.a
  178002. GABRIEL WEATHERHEAD
  178003. 12325
  178004. 13334N
  178005. 2/28/96V
  178006. Z. CHEM. 30(9), 1990 SYNTHESIS AND PROPERTIES OF SYM TRIAZO(1,5 A)PYRIMIDINES. FISCHER G PP. 305 15 (213 REFERENCES). IN GERMAN. A REVIEW.a
  178007. GABRIEL WEATHERHEAD
  178008. 12326
  178009. 13335N
  178010. 2/28/96VxTOP. CURR. CHEM. 156, 1990 PHOTOINDUCED ELECTRON TRANSFER OXYGENATIONS. LOPEZ L., PP. 117 66 (233 REFERENCES). A REVIEW.a
  178011. GABRIEL WEATHERHEAD
  178012. 12327
  178013. 13336N
  178014. 2/28/96V
  178015. TOP. CURR. CHEM. 156, 1990 PHOTOINDUCED ELECTRON TRANSFER OF CARBANIONS AND CARBOCATIONS. KROGH E., WAU P., PP. 93 116 (81 REFERENCES). A REVIEW.a
  178016. GABRIEL WEATHERHEAD
  178017. 12328
  178018. 13337N
  178019. 2/28/96V
  178020. TOP. CURR. CHEM. 156, 1990 PHOTOINDUCED ELECTRON TRANSFER (PET) BOND CLEAVAGE REACTIONS. SAEVA F. D., PP. 59 92 (97 REFERENCES). A REVIEW.a
  178021. GABRIEL WEATHERHEAD
  178022. 12329
  178023. 13338N
  178024. 2/28/96V
  178025. TOP. CURR. CHEM. 156, 1990 FUNDAMENTAL CONCEPTS OF PHOTOINDUCED ELECTRON TRANSFER. KAVARNOS G. J., PP. 21 58 (69 REFERENCES) A REVIEW.a
  178026. GABRIEL WEATHERHEAD
  178027. 12330
  178028. 13339N
  178029. 2/28/96V
  178030. TOP. CURR. CHEM. 155, 1990 A BRIEF HISTORY OF PHOTOINDUCED ELECTRON TRANSFER AND RELATED REACTIONS. ROTH H. D., PP. 1 19 (149 REFERENCES). A REVIEW.a
  178031. GABRIEL WEATHERHEAD
  178032. 12331
  178033. 13340N
  178034. 2/28/96V
  178035. TOP. CURR. CHEM. 155, 1990 THROUGH BOND MODULATION OF REACTION CENTERS BY REMOTE SUBSTITUENTS. HO T. L., PP. 81 158 (275 REFERENCES). A REVIEW.
  178036. GABRIEL WEATHERHEAD
  178037. 12332
  178038. 13341N
  178039. 2/28/96V
  178040. TOP. CURR. CHEM. 155, 1990 GEM DIHALOCYCLOPROPANES IN ORGANIC SYNTHESIS. KOSTIKOV R. R., MOLCHANOV A. P., HOPF H., PP. 41 80 (238 REFERENCES). A REVIEW.a
  178041. GABRIEL WEATHERHEAD
  178042. 12333
  178043. 13342N
  178044. 2/28/96V
  178045. TOP. CURR. CHEM. 154, 1990 METAL HOMOENOLATES FROM SILOXYCYCLOPROPANES. KUWAJIMA I., NAKAMURA E., PP. 1 39 (64 REFERENCES). A REVIEW.a
  178046. GABRIEL WEATHERHEAD
  178047. 12334
  178048. 13343N
  178049. 2/28/96V}TOP. CURR. CHEM. 154, 1990 SYNTHESIS OF DEOXY OLIGOSACCHARIDES. THIEM J., KLAFFKE W., PP. 285 332 (138 REFERENCES). A REVIEW.a
  178050. GABRIEL WEATHERHEAD
  178051. 12335
  178052. 13344N
  178053. 2/28/96VfTOP. CURR. CHEM. 154, 1990 CHEMISTRY OF PSEUDO SUGARS. SUAMI T., PP. 257 83 (55 REFERENCES). A REVIEW.a
  178054. GABRIEL WEATHERHEAD
  178055. 12336
  178056. 13345N
  178057. 2/28/96V
  178058. TOP. CURR. CHEM. 154, 1990 PREPARATION OF SELECTIVELY ALKYLATED SACCHARIDES AS SYNTHETIC INTERMEDIATES STANEK J., PP. 209 56 ( 449 REFERENCES). A REVIEW.
  178059. GABRIEL WEATHERHEAD
  178060. 12337
  178061. 13346N
  178062. 2/28/96VmTOP. CURR. CHEM. 154, 1990 SYNTHESIS OF GLYCOLIPIDS. GIGG J., GIGG R., PP. 77 139 (313 REFERENCES). A REVIEW.a
  178063. GABRIEL WEATHERHEAD
  178064. 12338
  178065. 13347N
  178066. 2/28/96VrTOP. CURR. CHEM. 154, 1990 SYNTHETIC SACCHARIDE PHOTOCHEMISTRY. DESCOLES G., PP. 39 76 (116 REFERENCES). A REVIEW.a
  178067. GABRIEL WEATHERHEAD
  178068. 12339
  178069. 13348N
  178070. 2/28/96V
  178071. CHEM. SOC. REV. 16(4), 1987 SYNTHESIS OF OLIGOSACCHARIDES RELATED TO BACTERIAL O ANTIGENS. BUNONE D. R., PP. 1 37 (137 REFERENCES) A REVIEW.a
  178072. GABRIEL WEATHERHEAD
  178073. 12340
  178074. 13349N
  178075. 2/28/96V
  178076. RES. CHEM. INTERMEDIATES 12(2), 1989 MODERN METHODS FOR THE INTRODUCTION OF FLUORINE INTO ORGANIC MOLECULES   AN APPROACH TO COMPOUNDS WITH ALTERED CHEMICAL AND BIOLOGICAI ACTIVITIES. MANN J.,PP. 381 436 (160 REFERENCES). A REVIEW.a
  178077. GABRIEL WEATHERHEAD
  178078. 12341
  178079. 13350N
  178080. 2/28/96
  178081. RES. CHEM. INTERMEDIATES 12(2), 1989 PHOTOCHEMISTRY AND PHOTOPHYSICS FROM THE EXCITED STATES OF DIARYL KETYL RADICALS NETTOFERREIRA J. C., SCAIANO J. C, PP. 187  201 (41 REFERENCES); A REVIEW.a
  178082. GABRIEL WEATHERHEAD
  178083. 12342
  178084. 13351N
  178085. 2/28/96V
  178086. RES. CHEM. INTERMEDIATES 12(2), 1989 STRUCTURE, SPECTROSCOPY AND KINETICS OF THE METHYLENE AMIDOGEN (H2CN) RADICAL. MARSTON G., STIEF L. J., PP. 161 86 (82 REFERENCES). A REVIEW.a
  178087. GABRIEL WEATHERHEAD
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  178089. 13352N
  178090. 2/28/96V
  178091. NATURAL PRODUCTS REPORTS 6(6) 1989 PROTONATED (PROTOSOLVATED) ONIUM LONS (ONIUM DICATIONS). OLAH G. A., PRAKASH G. K. S. LAMMERTSMA K., PP. 141 59 (49 REFERENCES). A REVIEW.a
  178092. GABRIEL WEATHERHEAD
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  178094. 13353N
  178095. 2/28/96V
  178096. NATURAL PRODUCTS REPORTS 6(6) 1989 RECENT ADVANCES IN THE USE OF ENZYME CATALYZED REACTION IN ORGANIC SYNTHESIS. TURNER N. J., PP. 625 44 (158 REFERENCES). A REVIEW.a
  178097. GABRIEL WEATHERHEAD
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  178100. 2/28/96
  178101. J SYN. ORG. CHEM. JPN. 49(2), 1991 STEROIDS   REACTIONS AND PARTIAL SYNTHESIS. TURNER A. B., PP. 539 75 (267 REFERENCES). NATURAL PRODUCTS REPORTS 6(6) 1989 PYRROLIZIDINE ALKALOIDS. ROBINS D. J., PP. 577 89 (101 REFERENCES). A REVIEW.a
  178102. GABRIEL WEATHERHEAD
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  178104. 13355N
  178105. 2/28/96V
  178106. J SYN. ORG. CHEM. JPN. 49(2), 1991 SYNTHESIS OF ENKEPHALIN ANALOGS WITH ABILITY TO RECOGNIZE DISCRIMINATIVELY THE OPIOID RECEPTOR SUBTYPES. SHIMOHIGASHI Y., PP. 147 57 (68 REFERENCES). IN JAPANESE. A REVIEW.a
  178107. GABRIEL WEATHERHEAD
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  178110. 2/28/96V
  178111. J SYN. ORG. CHEM. JPN. 49(2), 1991 LIVING POLYMERIZATION OF SUBSTITUTED ACETYLENES BY TRANSITION METAL CATALYSTS. MASUDA T., (37 REFERENCES). IN JAPANESE. A REVIEW.a
  178112. GABRIEL WEATHERHEAD
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  178115. 2/28/96
  178116. J SYN. ORG. CHEM. JPN. 49(2), 1991 DEVELOPMENT OF HIGHLY SELECTIVE METHODS FOR INTRODUCTION OF CARBON SUBSTITUENTS TO NITROGEN HETEROCYCLES BY MEANS OF ORGANOTIN REAGENTS AND APPLICATION TO SYNTHESIS OF NITROGEN POLYCYCLES. YAMAGUCHI R., PP 128 37 (36 REFERENCES). IN JAPANESE. A REVIEW.
  178117. GABRIEL WEATHERHEAD
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  178120. 2/28/96V
  178121. J SYN. ORG. CHEM. JPN. 49(2), 1991 VERSATILE CHIRAL SYNTHONS FOR 2 AMINO ALCOHOLS. ISHIZUKA T., KUNIEDA T., PP. 118 27( 30 REFERENCES). A REVIEW.a
  178122. GABRIEL WEATHERHEAD
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  178124. 13359N
  178125. 2/28/96V
  178126. J SYN. ORG. CHEM. JPN. 49(2), 1991 STEREOCHEMICAL CONTROL IN MICROBIAL REDUCTION. NAKAMURA K., OHMO A., PP. 110 7 (25 REFERENCES). IN JAPANESE. A REVIEW.a
  178127. GABRIEL WEATHERHEAD
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  178129. 13360N
  178130. 2/28/96V
  178131. ACTA. CHEM. SCAND. 44(8), L990 SYNTHETIC STUDIES ON OPTICALLY ACTIVE AND BIOLOGICALLY ACTIVE COMPOUNDS. TERASHIMA S.,PP. 98 109 (74 REFERENCES). A REVIEW.a
  178132. GABRIEL WEATHERHEAD
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  178136. J. ORGANOMETAL. CHEM. 392(1 3), 1990 RATES AND MECHANISMS OF ELECTRON TRANSFER/NICKEL CATALYZED HOMOCOUPLING AND CARBOXYLATION REACTIONS   AN ELECTROCHEMICAL APPROACH. AMATORE C., JUTAND A., PP. 755 64 (20 REFERENCES). A REVIEW.a
  178137. GABRIEL WEATHERHEAD
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  178139. 13362N
  178140. 2/28/96V
  178141. J. ORGANOMETAL. CHEM. 392(1 3), 1990 TRANSITION METALS IN ORGANIC SYNTHESIS   ANNUAL SURVEY COVERING THE YEAR 1989. HEGEDUS L. S., PP. 285 607 (992 REFERENCES). A REVIEW.a
  178142. GABRIEL WEATHERHEAD
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  178145. 2/28/96V
  178146. J. ORGANOMETAL. CHEM. 392(1 3), 1990 ORGANIC REACTIONS OF SELECTED PI COMPLEXES   ANNUAL SURVEY COVERING THE YEAR 1988. ROCKETT B. W., MARR G., PP. 161 283 (335 REFERENCES). A REVIEW.a
  178147. GABRIEL WEATHERHEAD
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  178149. 13364N
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  178151. J. ORGANOMETAL. CHEM. 392(1 3), 1990 FERROCENE   ANNUAL SURVEY COVERING THE YEAR 1988. MARR G., ROCKETT B. W., PP. 93 160 (174 REFERENCES). A REVIEW.a
  178152. GABRIEL WEATHERHEAD
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  178155. 2/28/96
  178156. J. ORGANOMETAL. CHEM. 392(1 3), 1990 LANTHANIDES AND ACTINIDES   ANNUAL SURVEY COVERING THE YEAR 1982. ERNST R. D., PP. 51 92 (75 REFERENCES). A REVIEW.a
  178157. GABRIEL WEATHERHEAD
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  178160. 2/28/96V
  178161. TETRAHEDRON ASYMMETRY 1(8), 1990 BORON   BORANES IN ORGANIC SYNTHESIS   ANNUAL SURVEY COVERING THE YEAR 1987. KABALKA G. W., GUINDI L. H. M., PP. 1 49 (135 REFERENCES). A REVIEW.a
  178162. GABRIEL WEATHERHEAD
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  178165. 2/28/96VmPOLYHEDRON 9(19) 1990 CHIRAL ACETALS IN ASYMMETRIC SYNTHESIS. ALEXAKIS A., MANGENEY P., PP. 477 511 A REVIEW.a
  178166. GABRIEL WEATHERHEAD
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  178170. N.M. PRZHEVAL'SKII AND I.I. GRANDBERG, RUSS. CHEM. REV., 56, 477 (1987). THE COPE AZA REARRANGEMENT IN ORGANIC SYNTHESIS. A REVIEW.a
  178171. GABRIEL WEATHERHEAD
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  178174. 2/28/96
  178175. R. DOLBIER, JR. ET AL., J. AM. CHEM. SOC., 109, 3046 (1987). KINETIC AND STEREOCHEMICAL EFFECT OF A FLUORINE SUBSTITUENT ON THE COPE AND THE HOMODIENYL 1,5 HYDROGEN SHIFT REARRANGEMENTS A REVIEW.a
  178176. GABRIEL WEATHERHEAD
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  178180. G.W. KABALKA, J. ORGANOMET. CHEM., 337, 169 (1987). BORANES IN ORGANIC SYNTHESIS. ANNUAL SURVEY COVERING THE YEAR 1985. PURE AND APPL. CHEM., 59, 837 914 (1987). 6TH INTERNATIONAL SYMPOSIUM ON BORON CHEMISTRY, BECHYNE, CZECHOSLOVAKIA, 22 26 JUNE 1987. A REVIEW.
  178181. GABRIEL WEATHERHEAD
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  178184. 2/28/96VfK. SMITH, CHEM. IND., 603 L987). ADVANCES IN ORGANOBORON CHEMISTRY   PROSPECTS FOR INDUSTRY. A REVIEW.a
  178185. GABRIEL WEATHERHEAD
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  178188. 2/28/96V
  178189. C.K. BRADSHER, CHEM. REV., 87, 1277 (1987). FORMATION OF SIX MEMBERED AROMATIC RINGS BY CYCLIALKYATION OF SOME ALDEHYDES AND KETONES. A REVIEW.a
  178190. GABRIEL WEATHERHEAD
  178191. 12364
  178192. 13373N
  178193. 2/28/96
  178194. T.C.W. MAK AND H.N.C. WONG, TOP. CURR. CHEM.. 140, 141 (1987). INCLUSION PROPERTIES OF TETRAPHENYLENE AND SYNTHESIS OF ITS DERIVATIVES. A REVIEW.a
  178195. GABRIEL WEATHERHEAD
  178196. 12365
  178197. 13374N
  178198. 2/28/96VXA. COLLET TETRAHEDRON, 43, 5725 (1987). CYCLOTRIVERATRYLENES AND CRYPTOPHANES. A REVIEW.a
  178199. GABRIEL WEATHERHEAD
  178200. 12366
  178201. 13375N
  178202. 2/28/96VkG.P. ELLIS AND T.M. ROMNEY ALEXANDER, CHEM. REV., 87, 779 (1987). CYANATION OF AROMATIC HALIDES.  A REVIEW.a
  178203. GABRIEL WEATHERHEAD
  178204. 12367
  178205. 13376N
  178206. 2/28/96V\J.J. MCCULLOUGH, CHEM. REV., 87, 811 (1987). PHOTOADDITIONS OF AROMATIC COMPOUNDS. A REVIEW.a
  178207. GABRIEL WEATHERHEAD
  178208. 12368
  178209. 13377N
  178210. 2/28/96VsV. RAMAMURTHY AND K. VENKATESAN, CHEM. REV. 87, 433 (1987).  PHOTOCHEMICAL REACTIONS OF ORGANIC CRYSTALS. A REVIEW.a
  178211. GABRIEL WEATHERHEAD
  178212. 12369
  178213. 13378N
  178214. 2/28/96
  178215. M.A. FOX ET AL., J. ORG. CHEM., 52, 1469 (1987). STERIC EFFECTS VS. SECONDARY ORBITAL OVERLAP IN DIELS ALDER REACTIONS. MNDO AND AM1 STUDIES. A REVIEW.a
  178216. GABRIEL WEATHERHEAD
  178217. 12370
  178218. 13379N
  178219. 2/28/96V
  178220. R.M. OTTENBRITE ET AL., J. ORG. CHEM., 52, 391 (1987). AN AB INITIO MOLECULAR ORBITAL EVALUATION OF LEWIS ACID CATALYSIS ON DIELS ALDER REACTIONS OF ACROLEIN. A REVIEW.a
  178221. GABRIEL WEATHERHEAD
  178222. 12371
  178223. 13380N
  178224. 2/28/96V
  178225. J. MLCOCH AND E. STECKHAN, TETRAHEDRON LETT., 28, 1081 (1987). ELECTROCHEMICALLY INDUCED [4+2] CYCLOADDITIONS A MECHANISTIC INTERPRETATION OF THE CATION RADICAL DIELS ALDER REACTION BASED ON PREPARATIVE RESULTS. A REVIEW.a
  178226. GABRIEL WEATHERHEAD
  178227. 12372
  178228. 13381N
  178229. 2/28/96
  178230. J.J. GAJEWSKI ET AL., J. AM. CHEM. SOC., 109, 5545 (1987). TRANSITION STATE STRUCTURE VARIATION IN THE DIE1S ALDER REACTION FROM SECONDARY DEUTERIUM KINETIC ISOTOPE EFFECTS: THE REACTION OF A NEARLY SYMMETRICAL DIENE AND DIENOPHILE IS NEARLY SYNCHRONOUS. A REVIEW.
  178231. GABRIEL WEATHERHEAD
  178232. 12373
  178233. 13382N
  178234. 2/28/96V
  178235. T. KOIZUMI ET AL., TETRAHEDRON LETT., 28, 3689 (1897). A DISPROOF OF KAHN HEHRE'S PROPOSAL ON THE GROUND STATE CONFORMATIONS AND THE STERIC COURSE OF THE DIELS ALDER REACTION OF VINYL SULFOXIDES. A REVIEW.a
  178236. GABRIEL WEATHERHEAD
  178237. 12374
  178238. 13383N
  178239. 2/28/96V
  178240. N.L. BAULD ET AL., J. AM. CHEM. SOC., 109, 4960 (1987). MECHANISTIC DIAGNOSIS OF AMINIUM SALT INITIATED DIELS ALDER CYCLOADDITIONS IN THE DIENE/DIENE FORMAT.  A REVIEW.a
  178241. GABRIEL WEATHERHEAD
  178242. 12375
  178243. 13384N
  178244. 2/28/96V
  178245. H. J. SCHNEIDER AND N.K. SANGWAN, ANGEW. CHEM., INT. ED. ENGL., 26, 896 (1987). CHANGES OF STEREOSELECTIVITY IN DIELS ALDER REACTIONS BY HYDROPHOBIC SOLVENT EFFECTS AND BY B CYCLODEXTRIN. A REVIEW.a
  178246. GABRIEL WEATHERHEAD
  178247. 12376
  178248. 13385N
  178249. 2/28/96
  178250. P. NANJAPPAN AND A.W. CZARNIK, J. AM. CHEM. SOC., 09, 1826 (1987). METAL ION CATALYZED REACTIONS OF ACRYLONITRILE, ACRYLAMIDE AND ETHYL ACRYLATE BY WAY OF THEIR DIELS ALDER CYCLOADDUCTS. A REVIEW.a
  178251. GABRIEL WEATHERHEAD
  178252. 12377
  178253. 13386N
  178254. 2/28/96V
  178255. R. SUSTMANN ET AL., CHEM. BER., 120, 1315 AND 1323 (1987). CHARGE TRANSFER COMPLEXES AND REACTIVITY IN DIELS ALDER CYCLOADDITIONS. A REVIEW.a
  178256. GABRIEL WEATHERHEAD
  178257. 12378
  178258. 13387N
  178259. 2/28/96V
  178260. K.V. RADHA KISHAN AND G.R. DESIRAJU, J. ORG. CHEM., 52, 4641 (1987). CRYSTAL ENGINEERING A SOLID STATE DIELS ALDER REACTION. A REVIEW.a
  178261. GABRIEL WEATHERHEAD
  178262. 12379
  178263. 13388N
  178264. 2/28/96VrS. MISUMI, PURE APPL. CHEM., 59, 1627 (1987). SYMPOSIUM LECTURE: CYCLOADDITION REACTIONS OF CYCLOPHANES. A REVIEW.a
  178265. GABRIEL WEATHERHEAD
  178266. 12380
  178267. 13389N
  178268. 2/28/96VfA. ICHIHARA, SYNTHESIS, 207 (1987). RETRO DIELS ALDER STRATEGY IN NATURAL PRODUCT SYNTHESIS. A REVIEW.a
  178269. GABRIEL WEATHERHEAD
  178270. 12381
  178271. 13390
  178272. 2/28/96VbN.L. BAULD ET AL., ACC. CHEM. RES., 20, 371 (1987). CATION RADICAL PERICYCLIC REACTIONS. A REVIEW.a
  178273. GABRIEL WEATHERHEAD
  178274. 12382
  178275. 13391N
  178276. 2/28/96V^J.L. CHARLTON AND M.M. ALAUDDIN, TETRAHEDRON, 43,2873 (1987).  ORTHOQUINODIMETHANES. A REVIEW.a
  178277. GABRIEL WEATHERHEAD
  178278. 12383
  178279. 13392N
  178280. 2/28/96V
  178281. A.J. FATIADI, SYNTHESIS, 749 (1987). ADDITION AND CYCLOADDITION REACTIONS OF TETRACYANOETHYLENE (TCNE) IN ORGANIC CHEMISTRY. A REVIEW.a
  178282. GABRIEL WEATHERHEAD
  178283. 12384
  178284. 13393N
  178285. 2/28/96VwD. CRAIG, CHEM. SOC. REV., 16, L87 (1987). STEREOCHEMICAL ASPECTS OF THE INTRAMOLECULAR DIELS ALDER REACTION. A REVIEW.a
  178286. GABRIEL WEATHERHEAD
  178287. 12385
  178288. 13394N
  178289. 2/28/96VqM.S. SALAKHOV AND S.A. ISMAILOV, RUSS. CHEM. REV., 55, 1145 (1986). INTRAMOLECULAR [4+2] CYCLOADDITION. A REVIEW.a
  178290. GABRIEL WEATHERHEAD
  178291. 12386
  178292. 13395N
  178293. 2/28/96VhA. DE MEIJERE, CHEM. BRIT., 23, 865 (1987). CYCLOPROPYL BUILDING BLOCKS FOR ORGANIC SYNTHESIS. A REVIEW.
  178294. GABRIEL WEATHERHEAD
  178295. 12387
  178296. 13396N
  178297. 2/28/96VuB. HALTON AND P.J. STANG, ACC. CHEM. RES., 20, 443 (1987). ALKYLIDENECYCLOPROPARENES AND RELATED COMPOUNDS. A REVIEW.a
  178298. GABRIEL WEATHERHEAD
  178299. 12388
  178300. 13397N
  178301. 2/28/96VuB.A. TROFIMOV, J. ORG. CHEM. (USSR), 22, 1788 (1986). MINI  SUPERBASIC MEDIA IN THE CHEMISTRY OF ACETYLENE. A REVIEW.a
  178302. GABRIEL WEATHERHEAD
  178303. 12389
  178304. TET. LETT.CNCYCLOPENTENONE WITTIG INTERNAL CYCLIZATION PREPARATION REVIEW HALO KETONE UEDAM
  178305. 13398N
  178306. 2/28/96V_CYCLOPENTENONE SYNTHESIS FROM ALLYLIDENE TRIPHENYLPHOSPHORANE AND ALPHA HALO CARBONYL COMPOUNDSW
  178307. P 4521 (1991)a
  178308. GABRIEL WEATHERHEAD
  178309. 12390
  178310. B    SYNTHESISCuREVIEW DIELS ALDER [2+2] CYCLOADDITION ENE REACTION ASYMMETRIC EPOXIDE CARBONYL LEWIS ACID CHIRAL AUXILLIARY NARASAKAM
  178311. 13399N
  178312. 2/28/96V4CHIRAL LEWIS ACIDS IN CATALYTIC ASYMMETRIC REACTIONSW
  178313. P 1 (1991)a
  178314. GABRIEL WEATHERHEAD
  178315. 12391
  178316. ORG PREP PROCEDURE INT
  178317. ALPHA NITRO KETONES ALPHA,BETA UNSATURATED CARBONYL COMPOUNDS CATALYZED ALLYLIC ALKYLATION SIDE CHAIN NITRATION MICHAEL ADDITION NEUTRAL CONDITIONS GENERAL SYNTHESIS RING ENLARGEMENT 1,5 DICARBONYL COMPOUNDS CONJUGATED NITROALKENES ROSINI GM
  178318. 13400N
  178319. 2/28/96VKRECENT PROGRESS IN THE SYNTHESIS AND REACTIVITY OF NITROKETONES   A REVIEW.W
  178320. 1990 DECX
  178321. 22(6)a
  178322. GABRIEL WEATHERHEAD
  178323. 12392
  178324. BULL SOC CHIM FRANCEC
  178325. CYCLOADDITION REACTIONS THERMAL ISOMERIZATION RING TRANSFORMATIONS CRYSTAL STRUCTURE BETA LACTAMS CHEMISTRY 1 HYDROXYAZETIDINES YNAMINES CONVERSION NUCLEOPHILES VERBOOM WM
  178326. 13401N
  178327. 2/28/96VA4 MEMBERED CYCLIC NITRONES   SYNTHESIS AND REACTIVITY   A REVIEW.W
  178328. 1990 NOV DECX
  178329. 704 713Y
  178330. GABRIEL WEATHERHEAD
  178331. 12393
  178332. BULL SOC CHIM FRANCE
  178333. ION CATALYZED HOMOLOGATION EPOXIDE CARBONYL REARRANGEMENT RING ENLARGEMENT REACTION CYCLIC KETONES PINACOL REARRANGEMENT DIAZOACETIC ESTERS ORIGINAL SYNTHESES REGIOSELECTIVE SYNTHESES ASYMMETRIC SYNTHESIS EFFICIENT SYNTHESIS KRIEF AM
  178334. 13402N
  178335. 2/28/96VSTRANSFORMATIONS OF BETA HYDROXYALKYL SELENIDES TO ALDEHYDES AND KETONES   A REVIEW.W
  178336. 1990 NOV DECX
  178337. 681 696Y
  178338. GABRIEL WEATHERHEAD
  178339. 12394
  178340. ORG PREP PROCEDURE INTC#ANNULATION CARVONE TRANS PODRAZA KFM
  178341. 13403N
  178342. 2/28/96V6REGIOSPECIFIC ALKYLATION OF CYCLOHEXENONES   A REVIEW.W
  178343. 1991 APRX
  178344. 23(2)a
  178345. GABRIEL WEATHERHEAD
  178346. 12395
  178347. ORG PREP PROCEDURE INT
  178348. ALPHA NITRO KETONES; ALPHA,BETA UNSATURATED CARBONYL COMPOUNDS; CATALYZED ALLYLIC ALKYLATION; SIDE CHAIN NITRATION; MICHAEL ADDITION; NEUTRAL CONDITIONS; GENERAL SYNTHESIS; RING ENLARGEMENT; 1,5 DICARBONYL COMPOUNDS; CONJUGATED NITROALKENEST 10 25/75 88; FLOW POLYAMIDE METHOD
  178349. 13404N
  178350. 2/28/96
  178351. VKRECENT PROGRESS IN THE SYNTHESIS AND REACTIVITY OF NITROKETONES   A REVIEW.W
  178352. 1990 DECX
  178353. 22(6)a
  178354. GABRIEL WEATHERHEAD
  178355. 12396
  178356. ORG PREP PROCEDURE INTC
  178357. DIASTEREOSELECTIVE CONJUGATE ADDITION; SILYL ETHER REARRANGEMENTS; RING CONTRACTION; MARASMIC ACID; ISOPRENE UNITS; LITHIUM TRIETHYLBOROHYDRIDE; PARA TOLUENESULFONATES; MYCINOLIDE IV; DERIVATIVES; 2,3 EPOXYCYCLOHEXANOLS MAGNUSSON GM
  178358. 13405N
  178359. 2/28/96VBREARRANGEMENTS OF EPOXY ALCOHOLS AND RELATED COMPOUNDS   A REVIEW.W
  178360. 1990 OCTX
  178361. 22(5)a
  178362. GABRIEL WEATHERHEAD
  178363. 12397
  178364. ANGEW. CHEM. INT. ED. ENGL.COCARBENE REVIEW INSERTION STEREOSPECIFIC MECHANISM FISHER CARBENE COMPLEX RESSIGM
  178365. 13406N
  178366. 2/28/96VaSTEREOSPECIFIC INSERTION OF THE CARBENE LIGAND OF A FISHER CARBENE COMPLEX INTO OLEFINIC C H BONDW
  178367. VOL 29   1990  PG 1129a
  178368. GABRIEL WEATHERHEAD
  178369. 12398
  178370. ANGEW. CHEM. INT. ED.ENGL.C=REVIEW CARBON MONOXIDE ORGANOMETALLIC CO COMPLEX METAL WERNERM
  178371. 13407N
  178372. 2/28/96
  178373. V`COMPLEXES OF CARBON MONOXIDE AND ITS RELATIVES: AN ORGANOMETALLIC FAMILY CELEBRATES ITS BIRTHDAYW
  178374. VOL 29   1990  PG 1077a
  178375. GABRIEL WEATHERHEAD
  178376. 12399
  178377. TET LETTCKCATALYST LEWIS ACID REVIEW WRITING DIELS ALDER LIBF4 LITHIUM CHELATION HOUKM
  178378. 13408N
  178379. 2/28/96VCLIBF4   A MILD LEWIS ACID FOR INTRAMOLECULAR DIELS ALDER  REACTIONSW
  178380. VOL 0   1991  PG 1549a
  178381. GABRIEL WEATHERHEAD
  178382. 12400
  178383. SYNLETTC?DIAZO KETONE CYCLIZATION TARGET REVIEW ADDITION AROMATIC MANDERM
  178384. 13409N
  178385. 2/28/96V;DIAZOKETONE CYCLIZATIONS AND THEIR AMPLICATION IN SYNTHESISW
  178386. VOL 0   1991  PG 134a
  178387. GABRIEL WEATHERHEAD
  178388. 12401
  178389. TET. LETT.CKADAM DIMETHYLDIOXIRANE DIOXIRANE EPOXIDATION OXYGEN TRANSFER EPOXIDE REVIEWM
  178390. 13410N
  178391. 2/28/96VSDIMETHYLDIOXIRANE EPOXIDATION OF ALKENES BEARING TWO ELECTRON DONATING SUBSTITUENTSW
  178392. VOL 0   1991  PG 1295a
  178393. GABRIEL WEATHERHEAD
  178394. 12402
  178395. JACSCWPAUSON KHAND ALKYNE CYCLOPENTENONE ORGANOMETALLIC COBALT REGIOSELECTIVITY REVIEW KRAFFTM
  178396. 13411N
  178397. 2/28/96
  178398. VFTHE DIRECTED PAUSON KHAND REACTION OF ALKENES ALKYNES, CO  AND COLBALTW
  178399. VOL 113   1991  PG 1693a
  178400. GABRIEL WEATHERHEAD
  178401. 12403
  178402. HETEROCYCLESCCFURAN ANNULATION ALLENE SULFONIUM REVIEW WRITING DIKETONE KANEMATSUM
  178403. 13412N
  178404. 2/28/96VJFURAN ANNULATION STRATEGY AN EFFICIENT SYNTHESIS OF FUSED  3 METHYL FURANSW
  178405. VOL 31   1990  PG 1003a
  178406. GABRIEL WEATHERHEAD
  178407. 12404
  178408. JOCCCWRITING ALCOHOL REVIEW DIKETENE DIOXINONE ACETOACETYLATION WITZEMANM
  178409. 13413N
  178410. 2/28/96V=TRANSACETATE WITH T BUTYL ACETOACETATE SYNTHETIC APPLICATIONSW
  178411. VOL 56   1991  PG 1713a
  178412. GABRIEL WEATHERHEAD
  178413. 12405
  178414. B    TET. LETTCMDIOXIRANE EPOXIDE WRITING REVIEW OXIDATION INTRODUCTION C H INSERTION MARPLESM
  178415. 13414N
  178416. 2/28/96V8DIOXIRANE MEDIATED ALKENE EPOXIDATION WITH A GOOD REVIEWW
  178417. VOL 91   1991  PG 533a
  178418. GABRIEL WEATHERHEAD
  178419. 12406
  178420. JACSCMEPOXIDE AZIRIDINE DEOXYGENATION REVIEW ORGANO TRANSITION METAL TUNGSTEN MAYERM
  178421. 13415N
  178422. 2/28/96
  178423. VPMECHANISM OF OXYGEN ATOM OR NITROGEN ATOM TRANSFER WITH   EPOXIDES OR AZIRIDINESW
  178424. VOL 113   1991  PG 870a
  178425. GABRIEL WEATHERHEAD
  178426. 12407
  178427. CHEM. COMM.C@AZIRIDINE REVIEW DIOL VICINAL CONVERSION SULFITE AZIDE REDUCTIONM
  178428. 13416N
  178429. 2/28/96V5SYNTHESIS OF HOMOCHIRAL AMINO ALCOHOLS AND AZIRIDINESW
  178430. VOL 95   1990  PG 0a
  178431. GABRIEL WEATHERHEAD
  178432. 12408
  178433. J. ORG .CHEM.C=ACYL SILANE SILICON REVIEW METHOD CARBANION ADDITION CARBONYLM
  178434. 13417N
  178435. 2/28/96VKA NEW METHOD FOR THE SYNTHESIS OF ACYL SILANES AND A REVIEW OF PAST METHODSW
  178436. VOL 56   1991  PG 1307a
  178437. GABRIEL WEATHERHEAD
  178438. 12409
  178439. TET LETTC@EPOXIDE CARBANION LITHIATE STANNANE TIN ADDITION CARBONYL REVIEWM
  178440. 13418N
  178441. 2/28/96V>GENERATION OF OXIRANYL LITHIUM COMPOUNDS FROM STANNYL EPOXIDESW
  178442. VOL 0   1991  PG 615a
  178443. GABRIEL WEATHERHEAD
  178444. 12410
  178445. SYN LETTCHRADICAL CYCLIZATION REVIEW SYNTHESIS TARGET RETROSYNTHESIS TANDEM CURRANM
  178446. 13419N
  178447. 2/28/96
  178448. VARADICAL REACTIONS AND RETROSYNTHETIC PLANNING   AN OVERALL REVIEWW
  178449. VOL 0   1991  PG 63a
  178450. GABRIEL WEATHERHEAD
  178451. 12411
  178452. SYN LETTC4WRITING REVIEW TIN ALLYL ACYL IRON 3+2 CYCLOADDITIONM
  178453. 13420N
  178454. 2/28/96VjEXPLORATION OF THE [3+2] CYCLOADDITION REACTION BETWEEN ALLYL STANNANES AND UNSATURATED ACYLIRON COMPLEXESW
  178455. VOL 0   1991  PG 1a
  178456. GABRIEL WEATHERHEAD
  178457. 12412
  178458. TET LETTCAAZIRIDINE REVIEW PREPARATION IMINE SILYL SILICON ADDITION ENOLATEM
  178459. 13421N
  178460. 2/28/96VkN METALLO IMINES   SYNTHESIS OF AZIRIDINES FROM N TRIMETHYLSILYL IMINES AND LITHIUM ENOLATES OF HALO ESTERSW
  178461. VOL 0   1991  PG 121a
  178462. GABRIEL WEATHERHEAD
  178463. 12413
  178464. JACSCPREAGENT CHIRAL EPOXIDATION EPOXIDE ASYMMETRIC SHARPLESS REVIEW TITANIUM TARTRATEM
  178465. 13422N
  178466. 2/28/96V?MECHANISM OF ASYMMETRIC EPOXIDATION USING THE SHARPLESS REAGENTW
  178467. VOL 113   1991  PG 106a
  178468. GABRIEL WEATHERHEAD
  178469. 12414
  178470. JOCCPALKALOID DIENE AZIDE INTRAMOLECULAR DIPOLAR CYCLOADDITION REVIEW NITRENE PEARSONM
  178471. 13423N
  178472. 2/28/96
  178473. V{INTRAMOLECULAR CYCLOADDITION OF AZIDES WITH ELECTRON RICH  DIENES   EQUIVALENT OF A NITRENE DIENE CYCLOADDITION FOR ALKALOIW
  178474. VOL 55   1990  PG 5719a
  178475. GABRIEL WEATHERHEAD
  178476. 12415
  178477. ANGEW. CHEM. INT. ED. ENGL.C;SYNTHESIS ARYL STRATEGY BIARYL CYCLIZATION REVIEW BRINGMANNM
  178478. 13424N
  178479. 2/28/96VJTHE DIRECTED SYNTHESIS OF BIARYL COMPOUNDS: MODERN CONCEPTS AND STRATEGIESW
  178480. VOL 29   1990  PG 977a
  178481. GABRIEL WEATHERHEAD
  178482. 12416
  178483. ACC. CHEM. RES.CFMETAL ENE YNE CYCLIZATION PALLADIUM REVIEW ALKYNE INTRAMOLECULAR TROSTM
  178484. 13425N
  178485. 2/28/96VHPALLADIUM CATALYZED CYCLOISOMERIZATIONS OF ENYNES AND RELATED  REACTIONSW
  178486. VOL 23   1990  PG 34a
  178487. GABRIEL WEATHERHEAD
  178488. 12417
  178489. ANGEW. CHEM. INT. ED. ENGLCHCARBOCATION REVIEW REACTION ADDITION MECHANISM REARRANGEMENT ALKENE MAYRM
  178490. 13426N
  178491. 2/28/96V%ADDITION OF CARBENIUM IONS TO ALKENESW
  178492. VOL 29   1990  PG 1371a
  178493. GABRIEL WEATHERHEAD
  178494. 12418
  178495. TET LETTC;DIOXIRANE OXIDATION REAGENT EPOXIDE EPOXIDATION REVIEW ADAMM
  178496. 13427
  178497. 2/28/96V0DIMETHYLDIOXIRANE EPOXIDATION OF ENOL PHOSPHATESW
  178498. VOL 0   1990  PG 6517a
  178499. GABRIEL WEATHERHEAD
  178500. 12419
  178501. CHEM REVCLCYCLOPROPANE ASYMMETRIC RHODIUM DIAZO TRANSITION METAL CARBENE REVIEW SALAUNM
  178502. 13428N
  178503. 2/28/96VoCOPPER OR RHODIUM CATALYZED DECOMPOSITION OF DIAZO COMPOUNDS IN THE SYNTHESIS OF OPTICALLY ACTIVE CYCLOPROPANESW
  178504. VOL 89   1989  PG 1247a
  178505. GABRIEL WEATHERHEAD
  178506. 12420
  178507. TETRAHEDRONC;BARRETT REVIEW NITRO RADICAL CYCLOADDITION SYNTHESIS ALKENEM
  178508. 13429N
  178509. 2/28/96V*NITROALKANES AND NITROALKENES IN SYNTHESISW
  178510. VOL 26   1990  PG 7313a
  178511. GABRIEL WEATHERHEAD
  178512. 12421
  178513. TETRAHEDRONCUCARDILLO CYCLIZATION ELECTROPHILIC METAL REVIEW STEREOSELECTIVE ALKENE INTRAMOLECULARM
  178514. 13430N
  178515. 2/28/96V[STEREOCONTROLLED CYCLOFUNCTIONALIZATIONS OF DOUBLE BONDS THROUGH HETEROCYCLIC INTERMEDIATESW
  178516. VOL 46   1990  PG 3321a
  178517. GABRIEL WEATHERHEAD
  178518. 12422
  178519. TETRAHEDRONCECHANON ELECTRON TRANSFER REVIEW PHYSICAL ORGANIC RADICAL CATION ANIONM
  178520. 13431N
  178521. 2/28/96
  178522. V#SINGLE ELECTRON TRANSFER   A REVIEWW
  178523. VOL 46   1990  PG 6193a
  178524. GABRIEL WEATHERHEAD
  178525. 12423
  178526. TETRAHEDRONCDTHEBTARANONTH REVIEW CYCLIZATION REACTION CATION RADICAL ANION METALM
  178527. 13432N
  178528. 2/28/96V%DEVELOPMENTS IN CYCLIZATION REACTIONSW
  178529. VOL 46   1990  PG 1385a
  178530. GABRIEL WEATHERHEAD
  178531. 12424
  178532. TETRAHEDRONC5ZHU REVIEW ASYMMETRIC ESTER HYDROLYSIS ENZYME REAGENTM
  178533. 13433N
  178534. 2/28/96V:APPLICATIONS OF PIG LIVER ESTERASE IN ASYMMETRIC SYNTHESISW
  178535. VOL 46   1990  PG 6587a
  178536. GABRIEL WEATHERHEAD
  178537. 12425
  178538. JOCC=CHIRAL OXAZIRIDINE REVIEW OXIDATION REAGENT HETEROCYCLE DAVISM
  178539. 13434N
  178540. 2/28/96VXCHEMISTRY OF OXAZIRIDINES   ASYMMETRIC OXIDATIONS USING HETEROCYCLIC CHIRAL OXAZIRIDINESW
  178541. VOL 56   1991  PG 809a
  178542. GABRIEL WEATHERHEAD
  178543. 12426
  178544. JOCCVEPOXIDE VINYLCYCLOPROPANE CONVERSION ALLYL ANION SULFIDE RING OPENING REVIEW SCHAUMANNM
  178545. 13435N
  178546. 2/28/96V-SYNTHESIS OF VINYLCYCLOPROPANES FROM EPOXIDESW
  178547. VOL 56   1991  PG 717a
  178548. GABRIEL WEATHERHEAD
  178549. 12427
  178550. JOCCAEPOXIDE REVIEW METAL PALLADIUM COUPLING RING OPENING CROSS LAROCKM
  178551. 13436N
  178552. 2/28/96VaPALLADIUM CATALYZED CROSS COUPLING OF ARYL HALIDES AND OLEFINIC  EPOXIDES VIA PALLADIUM MIGRATIONW
  178553. VOL 55   1990  PG 6244a
  178554. GABRIEL WEATHERHEAD
  178555. 12428
  178556. JOCCLBACKCOVER REVIEW DIOL ALCOHOL DEOXYGENATION REDUCTION BARTON REAGENT ALDRICHM
  178557. 13437N
  178558. 2/28/96VXDEOXYGENATION OF ALCOHOLS AND VICINAL DIOLS USING A VARIETY OF DIFFERENT REDUCING AGENTSW
  178559. VOL 55   1990  PG 6232a
  178560. GABRIEL WEATHERHEAD
  178561. 12429
  178562. JOCCOPUMMERER REVIEW SULFOXIDE SULFONIUM STEREOCHEM DIASTEREOCHEM THIONIUM HEATHCOCKM
  178563. 13438N
  178564. 2/28/96VISTEREOSELECTIVE ADDITIONS OF NUCLEOPHILIC ALKENES TO CHIRAL THIONIUM IONSW
  178565. VOL 55   1990  PG 5966a
  178566. GABRIEL WEATHERHEAD
  178567. 12430
  178568. JOCCWALLENE EPOXIDATION DIMETHYLDIOXIRENE EPOXIDE REVIEW CYCLIZATION INTRAMOLECULAR CRANDALLM
  178569. 13439N
  178570. 2/28/96V<ALLENE EPOXIDATION. OXIDATIVE CYCLIZATIONS OF ALLENYL ACIDESW
  178571. VOL 55   1990  PG 5929a
  178572. GABRIEL WEATHERHEAD
  178573. 12431
  178574. JOCCLHOMOLOGATION ALCOHOL METAL CATALYST CARBON MONOXIDE REVIEW INSERTION SILICONM
  178575. 13440N
  178576. 2/28/96VSA COBALT CATALYZED METHOD FOR THE HOMOLOGATION OF ALCOHOLS REVIEW OF THE LITERATUREW
  178577. VOL 55   1990  PG 5923a
  178578. GABRIEL WEATHERHEAD
  178579. 12432
  178580. JOCCKFURAN CARBENOID RHODIUM DIAZO CARBONYL ADDITION RING OPENING REVIEW WENKERTM
  178581. 13441N
  178582. 2/28/96VsMETAL CATALYZED REACTION OF FURANS AND ENOL ETHERS WITH ALPHA DIAZO CARBONYL COMPOUNDS CATALYZED BY RHODIUM ACETATEW
  178583. VOL 55   1990  PG 6203a
  178584. GABRIEL WEATHERHEAD
  178585. 12433
  178586. JOCCDTHIOAMIDE THIO PREPARATION REVIEW REAGENT LAWESSONS LAWESSON DEBRUINM
  178587. 13442N
  178588. 2/28/96VeA NEW ROUTE TO MONOSUBSTITUTED THIOAMIDES AND A REVIEW OF LITERATURE FOR OLDER METHODS OF PREPARATIONW
  178589. VOL 55   1990  PG 6091a
  178590. GABRIEL WEATHERHEAD
  178591. 12434
  178592. JOCCCCYCLOADDITION ALLYL CATION REVIEW 4+3 LEWIS TIN CHLORIDE GENERATIONM
  178593. 13443N
  178594. 2/28/96
  178595. V_4+3 CYCLOADDITION REACTION OF SOME SILYL ENOL ETHERS HAVING A  CONJUGATE CARBONYL FUNCTIONALITYW
  178596. VOL 55   1990  PG 6086a
  178597. GABRIEL WEATHERHEAD
  178598. 12435
  178599. PATAI SERIESCEALLENE SIGMATROPIC 2,3 REARRANGEMENT PERICYCLIC REVIEW COPE BRAVERMANM
  178600. 13444N
  178601. 2/28/96V REARRANGEMENTS INVOLVING ALLENESW
  178602. VOL 14   1989  PG 0a
  178603. GABRIEL WEATHERHEAD
  178604. 12436
  178605. CHEM. TRACTSCHEPOXIDE REVIEW RING OPENING PAYNE ALCOHOL REARRANGEMENT STEREOCHEM GANEMM
  178606. 13445N
  178607. 2/28/96VXISOMER SELECTIVITY IN THE STEREOCONTROLLED PAYNE REARRANGEMENT EPOXIDE CLEAVAGE REACTIONW
  178608. VOL 0   1990  PG 381a
  178609. GABRIEL WEATHERHEAD
  178610. 12437
  178611. CHEM. TRACTSCODIOXIRENE REAGENT OXIDIZING REVIEW DIMETHYLDIOXIRENE AMINE HYDROXYL AMINE GANEMM
  178612. 13446N
  178613. 2/28/96VaOXIDATION OF BIOLOGICALLY INTERESTING AMINES TO HYDROXYLAMINES USING DIMETHYLOXIRANE AS A REAGENTW
  178614. VOL 0   1990  PG 363a
  178615. GABRIEL WEATHERHEAD
  178616. 12438
  178617. CHEM TRACTS
  178618. CMEPOXIDE REVIEW CHIRAL EPOXIDATION CATALYST ASYMMETRIC ENANTIOSELECTIVITY HOUKM
  178619. 13447N
  178620. 2/28/96VYENANTIOSELECTIVE EPOXIDATION OF UNFUNCTIONALIZED ALKENES CATALYZED BY MANGANESE COMPLEXESW
  178621. VOL 0   1990  PG 350a
  178622. GABRIEL WEATHERHEAD
  178623. 12439
  178624. Tet. Lett.CDBUTENOLIDE TARGET EPOXIDE REVIEW RING OPENING CYCLIZATION ESTER CORYM
  178625. 13448N
  178626. 2/28/96V[A VERSATILE SYNTHESIS OF BUTENOLIDES FROM UNSATURATED ESTERS. EPOXIDATION AND REARRANGEMENTW
  178627. VOL 0   1990  PG 6789a
  178628. GABRIEL WEATHERHEAD
  178629. 12440
  178630. CHEM REVC@TRICARBONYL REVIEW PHOTOCHEM DIAZO DIELS ALDER TETRAKETONE RUBINM
  178631. 13449N
  178632. 2/28/96V$THE CHEMISTRY OF VICINAL POLYKETONESW
  178633. VOL 75   1975]   PG 177a
  178634. GABRIEL WEATHERHEAD
  178635. 12441
  178636. TETRAHEDRONCLVINYL SULFONE CONJUGATE ADDITION PREPARATION REVIEW DESULFONYLATION SIMPKINSM
  178637. 13450N
  178638. 2/28/96V7THE CHEMISTRY OF VINYL SULFONES. A BRIEF REVIEW ARTICLEW
  178639. VOL 46   1990  PG 6951a
  178640. GABRIEL WEATHERHEAD
  178641. 12442
  178642. TETRAHEDRON
  178643. CJREVIEW REAGENT KETENE HETEROATOM ACETAL KETENE ACETAL CYCLOADDITION ASOKANM
  178644. 13451N
  178645. 2/28/96V?OXOKETENE ACETALS. VERSATILE INTERMEDIATES IN ORGANIC SYNTHESISW
  178646. VOL 46   1990  PG 5423a
  178647. GABRIEL WEATHERHEAD
  178648. 12443
  178649. TETRAHEDRONC7REVIEW SYNTHESIS CYCLIZATION CYCLOADDITION THEBTARANOTHM
  178650. 13452N
  178651. 2/28/96V%DEVELOPMENTS IN CYCLIZATION REACTIONSW
  178652. VOL 46   1990  PG 1385a
  178653. GABRIEL WEATHERHEAD
  178654. 12444
  178655. TETRAHEDRONCNREVIEW DITHIANE CARBANION ALKYLATION DEPROTECTION HYDROLYSIS EQUIVALENT BULMANM
  178656. 13453N
  178657. 2/28/96VASYNTHETIC USES OF THE 1,3 DITHIANE GROUP FROM 1977 1988  A REVIEWW
  178658. VOL 45   1989  PG 7643a
  178659. GABRIEL WEATHERHEAD
  178660. 12445
  178661. TETRAHEDRONCHREVIEW CATALYST ORGANOMETALLIC REAGENT CHIRAL ASYMMETRIC SYNTHESIS OJIMAM
  178662. 13454N
  178663. 2/28/96VXRECENT ADVANCES IN CATALYTIC ASYMMETRIC REACTIONS PROMOTED BY TRANSITION METAL COMPLEXESW
  178664. VOL 45   1989  PG 6901a
  178665. GABRIEL WEATHERHEAD
  178666. 12446
  178667. TETRAHEDRON
  178668. CGOXIDATION REVIEW CHIRAL OXAZIRIDINE SULFONYL INDUCTION ASYMMETRIC DAVISM
  178669. 13455N
  178670. 2/28/96V1APPLICATIONS OF OXAZIRIDINES IN ORGANIC SYNTHESISW
  178671. VOL 45   1989  PG 5703a
  178672. GABRIEL WEATHERHEAD
  178673. 12447
  178674. TETRAHEDRONC*REVIEW REAGENT COUNTERATTACK SYNTHESIS HWUM
  178675. 13456N
  178676. 2/28/96V+COUNTERATTACK REAGENTS IN ORGANIC SYNTHESISW
  178677. VOL 45   1989  PG 1233a
  178678. GABRIEL WEATHERHEAD
  178679. 12448
  178680. TETRAHEDRONCODIELS ALDER SULFONE DEPROTECTION DESULFONYLATION REVIEW CYCLOADDITION DE LUCCHIM
  178681. 13457N
  178682. 2/28/96VbTHE ROLE OF SULFUR FUNCTIONALITIES IN ACTIVATING AND DIRECTING  OLEFINS IN CYCLOADDITION REACTIONSW
  178683. VOL 44   1988  PG 6755a
  178684. GABRIEL WEATHERHEAD
  178685. 12449
  178686. TETRAHEDRONC8REVIEW VINYL ANION ADDITION CARBONYL METHOD ENONE DREWESM
  178687. 13458N
  178688. 2/28/96ViSYNTHETIC POTENTIAL OF THE TERTIARY AMINE CATALYZED REACTION OF ACTIVATED VINYL CARBANIONS WITH ALDEHYDESW
  178689. VOL 44   1988  PG 4653a
  178690. GABRIEL WEATHERHEAD
  178691. 12450
  178692. B    SYNTHESIS
  178693. CECARBANION DIONE DICARBONYL DIKETONE ALKYLATION AMBIDENT REVIEW SCHICKM
  178694. 13459N
  178695. 2/28/96V9SYNTHESES AND REACTIONS OF 2 ALKYL 1,3 CYCLOPENTANEDIONESW
  178696. VOL 7   1989  PG 477a
  178697. GABRIEL WEATHERHEAD
  178698. 12451
  178699. B#ORGANIC PREPARATIONS AND PROCEDURESCRHALLER BAUER AMIDE CARBOXYLIC ACID SAPONIFICATION CLEAVAGE SYNTHESIS REVIEW GILDAYM
  178700. 13460N
  178701. 2/28/96VFCARBON CARBON BOND CLEAVAGE BY THE HALLER BAUER AND RELATED  REACTIONSW
  178702. VOL 22   1990  PG 167a
  178703. GABRIEL WEATHERHEAD
  178704. 12452
  178705. HETEROCYCLESCKLITHIATE METALLATION CHELATION HETEROCYCLE ALKYLATION METAL REVIEW BENNECHEM
  178706. 13461N
  178707. 2/28/96VTMETALLATION AND METAL ASSISTED BOND FORMATION IN PI ELECTRON  DEFICIENT HETEROCYCLESW
  178708. VOL 30   1990  PG 1155a
  178709. GABRIEL WEATHERHEAD
  178710. 12453
  178711. HETEROCYCLESCMDIPOLAR CYCLOADDITION NITRILE OXIDE DIPOLE REVIEW TARGET INTRAMOLECULAR TSUGEM
  178712. 13462N
  178713. 2/28/96VIRECENT ADVANCES IN SYNTHETIC APPLICATIONS OF NITRILE OXIDE CYCLOADDITIONSW
  178714. VOL 30   1990  PG 719a
  178715. GABRIEL WEATHERHEAD
  178716. 12454
  178717. HETEROCYCLESC?ANION IMINE ESTER ENOLATE ADDITION CARBONYL CONDENSATION REVIEWM
  178718. 13463N
  178719. 2/28/96V5LITERATURE REVIEW OF ESTER ENOLATE IMINE CONDENSATIONW
  178720. VOL 29   1989  PG 2225a
  178721. GABRIEL WEATHERHEAD
  178722. 12455
  178723. JOCCUPROSTAGLANDIN CYCLOPENTENONE CUPRATE ALKYLATION REVIEW INTRODUCTION WRITING PATTERSONM
  178724. 13464N
  178725. 2/28/96V\SYNTHESIS OF PROSTAGLANDINS BY CONJUGATE ADDITION AND ALKYLATION   OF A DIRECTED ENOLATE IONW
  178726. VOL 55   1990  PG 5528a
  178727. GABRIEL WEATHERHEAD
  178728. 12456
  178729. JOCC^RADICAL CLOCK CYCLOPROPYL CARBINYL RING OPENING RATE REVIEW INTRODUCTION PHYSICAL ORGANIC BEAKM
  178730. 13465N
  178731. 2/28/96VZREARRANGEMENT OF RIGID CYCLOPROPYL CARBINYL RADICALS   DETECTION   OF SHORT LIVED RADICALSW
  178732. VOL 55   1990  PG 5454a
  178733. GABRIEL WEATHERHEAD
  178734. 12457
  178735. TETRAHEDRONCEREVIEW ISOBENZOFURAN METHODOLOGY DIELS ALDER TARGET SYNTHESIS RODRIGOM
  178736. 13466N
  178737. 2/28/96V]PROGRESS IN THE CHEMISTRY OF ISOBENZOFURANS APPLICATIONS TO THE SYNTHESIS OF NATURAL PRODUCTS
  178738. VOL 44   1988  PG 2093a
  178739. GABRIEL WEATHERHEAD
  178740. 12458
  178741. TETRAHEDRONCHREVIEW THF TETRAHYDROFURAN POLYCYCLIC ETHER ANTIBIOTIC SPIROKETAL BUIVINM
  178742. 13467N
  178743. 2/28/96VcSYNTHETIC ROUTES TO TETRAHYDROFURAN, TETRAHYDROPYRAN AND  SPIROKETAL UNITS OF POLYETHER ANTIBIOTICSW
  178744. VOL 43   1987  PG 3309a
  178745. GABRIEL WEATHERHEAD
  178746. 12459
  178747. TETRAHEDRONCCREVIEW CHIRAL INDUCTION BICYCLIC CAMPHOR SULTAM ASYMMETRIC OPPOLZERM
  178748. 13468N
  178749. 2/28/96VACAMPHOR DERIVATIVES AS CHIRAL AUXILIARIES IN ASYMMETRIC SYNTHESISW
  178750. VOL 43   1987  PG 1969a
  178751. GABRIEL WEATHERHEAD
  178752. 12460
  178753. TETRAHEDRONCHREVIEW SULFONE WRITING CARBANION UNSATURATED VINYL CYCLOADDITION ROBERTSM
  178754. 13469N
  178755. 2/28/96V
  178756. SULFONE CHEMISTRY   A REVIEWW
  178757. VOL 43   1987  PG 1027a
  178758. GABRIEL WEATHERHEAD
  178759. 12461
  178760. TETRAHEDRONCBREVIEW SULFOXIDE OXIDATION SULFIDE THIO SULFUR REAGENT MADESCLAIREM
  178761. 13470N
  178762. 2/28/96V2SYNTHESIS OF SULFOXIDES BY OXIDATION OF THIOESTERSW
  178763. VOL 42   1986  PG 5459a
  178764. GABRIEL WEATHERHEAD
  178765. 12462
  178766. TETRAHEDRONC.OXY ALLYL CATION REVIEW CYCLOADDITION 4+2 MANNM
  178767. 13471N
  178768. 2/28/96V)THE SYNTHETIC UTILITY OF OXYALLYL CATIONSW
  178769. VOL 42   1986  PG 4611a
  178770. GABRIEL WEATHERHEAD
  178771. 12463
  178772. TETRAHEDRONC:REVIEW PALLADIUM SYNTHESIS ALLYL COMPLEX METHODOLOGY TSUJIM
  178773. 13472N
  178774. 2/28/96VkNEW GENERAL METHODS INVOLVING PI ALLYL PALLADIUM COMPLEXES AS INTERMEDIATES AND NEUTRAL REACTION CONDITIONSW
  178775. VOL 42   1986  PG 4361a
  178776. GABRIEL WEATHERHEAD
  178777. 12464
  178778. JOCC?OXIRANE RING OPENING REVIEW TANDEM BARTON ALCOHOL RADICAL RAWALM
  178779. 13473N
  178780. 2/28/96VLSYNTHESIS OF CARBOCYCLIC SYSTEMS VIA RADICAL INDUCED EPOXIDE   FRAGMENTATIONW
  178781. VOL 55   1990  PG 5181a
  178782. GABRIEL WEATHERHEAD
  178783. 12465
  178784. TETRAHEDRONCOREVIEW IMINIUM ALKALOID STEREOSELECTIVE ALKYNE OVERMAN REARRANGEMENT THIOIUMIONM
  178785. 13474N
  178786. 2/28/96VMCATIONIC CYCLIZATIONS OF IMINIUM IONS AND THEIR 3,3 SIGMATROPIC COPE REACTIONW
  178787. VOL 46   1990  PG 1385a
  178788. GABRIEL WEATHERHEAD
  178789. 12466
  178790. TETRAHEDRON
  178791. 'C@REAGENT FLAVONE NATURAL PROUDCTS FORMYLATION METAL COMPLEX DIAZOM
  178792. 13475N
  178793. 2/28/96V#ACETIC FORMIC ANHYDRIDE REVIEW  C13W
  178794. VOL 46   1990  PG 1081a
  178795. GABRIEL WEATHERHEAD
  178796. 12467
  178797. JOCC7 REVIEW COHEN EPOXIDE REDUCTIVE CLEAVAGE REGIOSELECTIVEM
  178798. 13476N
  178799. 2/28/96V8REDUCTIVE THIATION OF DIEPOXIDES TO FORM LITHIOALKOXIDESW
  178800. VOL 55 1990 PG 1528a
  178801. GABRIEL WEATHERHEAD
  178802. 12468
  178803. )B    SYNTHESISCJREVIEW CHIRAL INDUCTION ASYMMETRIC CYCLOADDITION SYNTHESIS WRITING TASHNERM
  178804. 13477N
  178805. 2/28/96V;ADVANCES IN ORG. SYNTHESIS ASYMMETRIC DIELS ALDER REACTIONSW
  178806. VOL 0   1989  PG 0a
  178807. GABRIEL WEATHERHEAD
  178808. 12469
  178809. ADVANCES IN ORG. SYNTHESISCCREVIEW PRESSURE ULTRA SOUND CYCLOADDITION SYNTHESIS WRITING GIGUEREM
  178810. 13478N
  178811. 2/28/96VDULTRASOUND, HIGH PRESSURE AND MICROWAVE HEATING IN ORGANIC SYNTHESISW
  178812. VOL 0   1989  PG 0a
  178813. GABRIEL WEATHERHEAD
  178814. 12470
  178815. TOPICS IN CURRENT CHEMISTRYCBSYNTHESIS REVIEW ALKALOID AMINE METHOXY CATION RADICAL ELECTROCHEMM
  178816. 13479N
  178817. 2/28/96
  178818. +VQSYNTHESIS OF ALKALOIDAL COMPOUNDS USING AN ELECTROCHEMICAL REACTION AS A KEY STEPW
  178819. VOL 0   1990]  PG 0a
  178820. GABRIEL WEATHERHEAD
  178821. 12471
  178822. TETRAHEDRONC&SILICON COUNTERATTACK DISPLACEMENT HWUM
  178823. 13480N
  178824. 2/28/96V=COUNTERATTACK REAGENTS IN ORGANIC SYNTHESIS REVIEW    REAGENTW
  178825. VOL 45   1989  PG 1233a
  178826. GABRIEL WEATHERHEAD
  178827. 12472
  178828. -B    SYNTHESISC8BROMO ESTER REFORMATSKY EXPERIMENTAL SYNTHESIS FUERSTNERM
  178829. 13481N
  178830. 2/28/96V<RECENT ADVANCES IN THE REFORMATSKY REACTION ZINC      REVIEWW
  178831. VOL 8   1989  PG 571a
  178832. GABRIEL WEATHERHEAD
  178833. 12473
  178834. CHEM. REV.C#NITRILE DIPOLE REVIEW SULFUR  PATONM
  178835. 13482N
  178836. 2/28/96VBTHE CHEMISTRY OF NITRILE SULFIDES DIPOLAR CYCLOADDITION    SULFIDEW
  178837. VOL 89   1989  PG 33a
  178838. GABRIEL WEATHERHEAD
  178839. 12474
  178840. CHEM. REV.CHVINYL CYCLOPROPANE CYCLOPENTENE REARRANGEMENT REVIEW THERMAL GOLDSCHMIDTM
  178841. 13483N
  178842. 2/28/96V5VINYLCYCLOPROPANE REARRANGEMENTS IN ORGANIC SYNTHESISW
  178843. VOL 88   1988  PG 229a
  178844. GABRIEL WEATHERHEAD
  178845. 12475
  178846. CHEM. REV.C:REVIEW CONFORMATION ALLYL STEREOCHEM 1,3  STRAIN BOLTZMANNM
  178847. 13484N
  178848. 2/28/96VMALLYLIC 1,3 STRAIN AS A CONTROLLING FACTOR IN STEREOSELECTIVE TRANSFORMATIONSW
  178849. VOL 89   1989  PG 1841a
  178850. GABRIEL WEATHERHEAD
  178851. 12476
  178852. CHEM. REV.C$KETAL SYNTHESIS PREPARATION ALBIZATIM
  178853. 13485N
  178854. 2/28/96V*CHEMISTRY OF SPIRO KETALS SPIRO     REVIEWW
  178855. VOL 89   1989  PG 1617a
  178856. GABRIEL WEATHERHEAD
  178857. 12477
  178858. CHEM. REV.C<HWU SILICON REVIEW STERIC TRIMETHYL SILYL SILYL DESILYLATIONM
  178859. 13486N
  178860. 2/28/96VASTERIC INFLUENCE OF THE TRIMETHYL SILYL GROUP INORGANIC REACTIONSW
  178861. VOL 89   1989  PG 1599a
  178862. GABRIEL WEATHERHEAD
  178863. 12478
  178864. CHEM. REV.CDWEINREB DIELS ALDER HETERO IMINE REVIEW ALKALOID IMINE CYCLOADDITIONM
  178865. 13487N
  178866. 2/28/96VFN ACYL IMINES AND RELATED HETERO DIENES IN 4+2 CYCLOADDITION CHEMISTRYW
  178867. VOL 89   1989  PG 1525a
  178868. GABRIEL WEATHERHEAD
  178869. 12479
  178870. CHEM. REV.C>PINACOL COUPLING ALKENE CARBONYL TITANIUM METAL REAGENT REVIEWM
  178871. 13488N
  178872. 2/28/96
  178873. 4V5CARBANYL COUPLING REACTIONS USING LOW VALENT TITANIUMW
  178874. VOL 89   1989  PG 1513a
  178875. GABRIEL WEATHERHEAD
  178876. 12480
  178877. CHEM. REV.CKVINYL EPOXIDE RING OPENING CUPRATE DISPLACEMENT SUBSTITUTION OXIRANE REVIEWM
  178878. 13489N
  178879. 2/28/96V=SN2 PRIME ADDITION OF ORGANO COPPER REAGENTS TOVINYL OXIRANESW
  178880. VOL 89   1989  PG 1503a
  178881. GABRIEL WEATHERHEAD
  178882. 12481
  178883. CHEM. REV.CCIMINE LACTAM PREPARATION 2+2 CARBANION ENOLATE CYCLOADDITION REVIEWM
  178884. 13490N
  178885. 2/28/96V6ESTER ENOLATE IMINE CONDENSATION ROUTE TO BETA LACTAMSW
  178886. VOL 89   1989  PG 1447a
  178887. GABRIEL WEATHERHEAD
  178888. 12482
  178889. CHEM. REV.C?RADICAL CYCLIZATION ALCOHOL REAGENT SULFUR THIO CARBONYL REVIEWM
  178890. 13491N
  178891. 2/28/96V8RADICAL CHEMISTRY ASSOCIATED WITH THE THIOCARBONYL GROUPW
  178892. VOL 89   1989  PG 1413a
  178893. GABRIEL WEATHERHEAD
  178894. 12483
  178895. CHEM. REV.C>BENZO AROMATIC CYCLOPROPENE PREPARATION REACTIVITY ELIMINATIONM
  178896. 13492N
  178897. 2/28/96V8DEVELOPMENTS INCYCLOPROPARENE CHEMISTRY REVIEW    STRAINW
  178898. VOL 89   1989  PG 1161
  178899. GABRIEL WEATHERHEAD
  178900. 12484
  178901. CHEM. REV.C3BICYCLIC BRIDGE ALKENE CYCLOADDITION TORSION REVIEWM
  178902. 13493N
  178903. 2/28/96V0STRAINED BRIDGEHEAD DOUBLE BONDS STRAIN    BREDTW
  178904. VOL 89   1989  PG 1067a
  178905. GABRIEL WEATHERHEAD
  178906. 12485
  178907. CHEM. REV.CKPHOSPHOROUS REVIEW WITTIG REAGENT CONDITIONS EXPERIMENTAL ALKENE CONVERSIONM
  178908. 13494N
  178909. 2/28/96V\THE WITTIG OLEFINATION REACTION AND MODIFICATIONS INVOLVING PHOSPHORYL STABILIZED CARBANIONSW
  178910. VOL 89   1989  PG 863a
  178911. GABRIEL WEATHERHEAD
  178912. 12486
  178913. CHEM. REV.CVDIPOLAR CYCLOADDITION REVIEW AZOMETHINE YLIDE PYRIDINE HYDROXY 6+4 DIMERIZATION DENNISM
  178914. 13495N
  178915. 2/28/96V<CYCLOADDITION REACTIONS OF HETEROAROMATIC SIX MEMBERED RINGSW
  178916. VOL 89   1989  PG 827a
  178917. GABRIEL WEATHERHEAD
  178918. 12487
  178919. ADV. IN HETEROCYCLIC CHEM.C-  PYRIDINE HETEROAROMATIC SUBSTITUTION REVIEWM
  178920. 13496N
  178921. 2/28/96VK REGIOSELECTIVE SUBSTITUTION IN AROMATIC SIX MEMBERED NITROGEN HETEROCYCLESW
  178922. VOL 44 1988 PG 199a
  178923. GABRIEL WEATHERHEAD
  178924. 12488
  178925. JOCCGEPOXIDE REVIEW RING OPENING TELLURIDE ALKENE CHIRAL RACEMATE RESOLUTIONM
  178926. 13497N
  178927. 2/28/96V|STEREOSPECIFIC TELLURIDE MEDIATED CONVERSION OF EPOXIDES TO ALLYL ALCOHOLS. AN EXTENSION OF THE SHARPLESS KINETIC RESOLUTIONW
  178928. VOL 55   1990  PG 1414a
  178929. GABRIEL WEATHERHEAD
  178930. 12489
  178931. TET LETTCZAZOMETHINE YLIDE CARBENE PYRIDINE REVIEW THIOCARBONYL YLIDE DIPHENYLCARBENE KINETICS PLATZM
  178932. 13498N
  178933. 2/28/96VSTHE KINETICS OF YLIDE FORMING REACTION BETWEEN TRIPLET DIPHENYLCARBENE AND PYRIDINEW
  178934. VOL 0   1990  PG 953a
  178935. GABRIEL WEATHERHEAD
  178936. 12490
  178937. JOCCGOXAZIRIDINE OXIDATION REAGENT REVIEW SULFONE PHENYLSULFONYL IMINE DAVISM
  178938. 13499N
  178939. 2/28/96VdCHEMISTRY OF OXAZIRIDINES. SYNTHESIS, REACTIONS AND CHIRAL INDUCTION OF SULFONYL SUBSTITUTED SYSTEMSW
  178940. VOL 55   1990  PG 1254a
  178941. GABRIEL WEATHERHEAD
  178942. 12491
  178943. SYN LETTCESILICONE SILANE ALLYL ADDITION CARBONYL FLUORIDE DESILYLATION SAKURAIM
  178944. 13500N
  178945. 2/28/96VIA REVIEW OF THE SAKURAI REACTION USING ALLYLIC SILANES WITH ELECTROPHILES
  178946. VOL 1   1989  PG 1a
  178947. GABRIEL WEATHERHEAD
  178948. 12492
  178949. SYN LETTCcVINYL REARRANGEMENT ALLENE DIELS ALDER CYCLIZATION INTRAMOLECULAR SULFOXIDE 2,3 SIGMATROPIC OKAMURAM
  178950. 13501N
  178951. 2/28/96ViPERICYCLIZATION OF VINYLALLENES IN ORGANIC SYNTHESIS ON THE INTRAMOLECULAR DIELS ALDER REACTION. A REVIEWW
  178952. VOL 1   1990  PG 1a
  178953. GABRIEL WEATHERHEAD
  178954. 12493
  178955. TET LETTERSCFEPOXIDE OXIRANE PAYNE RING OPENING CYCLIZATION STEREOCHEM NOVEL REVIEWM
  178956. 13502N
  178957. 2/28/96VaSTEREOSELECTIVE SYNTHESIS OF OXAZOLIDINONES VIA TANDEM CYCLIZATION SEQUENTIAL PAYNE REARRANGEMENTW
  178958. VOL 0   1990  PG 515a
  178959. GABRIEL WEATHERHEAD
  178960. 12494
  178961. JOCCFEPOXIDE PREPARATION REVIEW RADICAL CLOSURE ORGANOMETALLIC METAL SNIDERM
  178962. 13503N
  178963. 2/28/96VEPREPARATION OF EPOXIDES BY OXIDATIVE DECARBONYLATION OF HYDROXY ACIDSW
  178964. VOL 55   1990  PG 1965a
  178965. GABRIEL WEATHERHEAD
  178966. 12495
  178967. JOCCADIAZO KETONE AZIDE TRANSFER REVIEW EXPERIMENTAL WRITING DANHEISERM
  178968. 13504N
  178969. 2/28/96
  178970. DV;AN IMPROVED METHOD FOR THE SYNTHESIS OF ALPHA DIAZO KETONESW
  178971. VOL 55   1990  PG 1959a
  178972. GABRIEL WEATHERHEAD
  178973. 12496
  178974. TET LETTERSCESILYL EPOXIDE AZIDE RING OPENING ELIMINATION VINYL REVIEW CHAKRABORTYM
  178975. 13505N
  178976. 2/28/96VBREGIOSELECTIVE RING OPENING OF SILYL EPOXY ALCOHOLS WITH AZIDE IONW
  178977. VOL 0   1990  PG 1335a
  178978. GABRIEL WEATHERHEAD
  178979. 12497
  178980. REC TRAV. CHIM.C1REVIEW ZEOLITE SYNTHESIS PREPARATION EXPERIMENTALM
  178981. 13506N
  178982. 2/28/96V$USE OF ZEOLITES IN ORGANIC REACTIONSW
  178983. VOL 108   1989  PG 283a
  178984. GABRIEL WEATHERHEAD
  178985. 12498
  178986. CHEM. REV.CDHETEROCYCLE REVIEW ALKALOID PYRROLIZIDINE NIH BIOLOGY BIOCHEM ROBINSM
  178987. 13507N
  178988. 2/28/96V'BIOSYNTHESIS OF PYRROLIZIDINE ALKALOIDSW
  178989. VOL 89   1989  PG 375a
  178990. GABRIEL WEATHERHEAD
  178991. 12499
  178992. CHEM. REV.CEREVIEW SPIRO KETAL PREPARATION SYNTHESIS CARBONYL PROTECTION ALBIZATIM
  178993. 13508N
  178994. 2/28/96V
  178995. CHEMISTRY OF SPIROKETALSW
  178996. VOL 89   1989  PG 1617a
  178997. GABRIEL WEATHERHEAD
  178998. 12500
  178999. CHEM. REV.
  179000. IC.REVIEW STERIC HINDRANCE SILICON SILYL SIZE HWUM
  179001. 13509N
  179002. 2/28/96VBSTERIC INFLUENCE OF THE TRIMETHYL SILYL GROUP IN ORGANIC REACTIONSW
  179003. VOL 89   1989  PG 1599a
  179004. GABRIEL WEATHERHEAD
  179005. 12501
  179006. CHEM. REV.CJBORON ORGANOBORON REDUCTION CHIRAL ASYMMETRIC HYDROBORATION REVIEW MIDLANDM
  179007. 13510N
  179008. 2/28/96V0ASYMMETRIC REDUCTIONS WITH ORGANOBORANE REAGENTSW
  179009. VOL 89   1989  PG 1553a
  179010. GABRIEL WEATHERHEAD
  179011. 12502
  179012. CHEM. REV.CGDIELS ALDER IMINE REVIEW CYCLOADDITION HETEROCYCLIC SCHIFF BASE WEINREBM
  179013. 13511N
  179014. 2/28/96VEN ACYLIMINES AND RELATED HETERO DIENES IN 4+2 CYCLOADDITION REACTIONSW
  179015. VOL 89   1989  PG 1525a
  179016. GABRIEL WEATHERHEAD
  179017. 12503
  179018. CHEM. REV.CLREVIEW SUBSTITUTION EPOXIDE CUPRATE RING OPENING VINYL DISPLACEMENT MARSHALLM
  179019. 13512N
  179020. 2/28/96V:SN2' APPROACHES OF ORGANOCOPPER REAGENTS TO VINYL OXIRANESW
  179021. VOL 89   1989  PG 1503a
  179022. GABRIEL WEATHERHEAD
  179023. 12504
  179024. CHEM. REV.C<2+2 IMINE LACTAM ENOLATE CYCLOADDITION SYNTHESIS REVIEW HARTM
  179025. 13513N
  179026. 2/28/96
  179027. MV:THE ESTER ENOLATE IMINE CONDENSATION ROUTE TO BETA LACTAMSW
  179028. VOL 89   1989  PG 1447a
  179029. GABRIEL WEATHERHEAD
  179030. 12505
  179031. CHEM. REV.C5THIO SULFUR RADICAL CYCLIZATION REVIEW CARBONYL CRICHM
  179032. 13514N
  179033. 2/28/96V8RADICAL CHEMISTRY ASSOCIATED WITH THE THIOCARBONYL GROUPW
  179034. VOL 89   1989  PG 1413a
  179035. GABRIEL WEATHERHEAD
  179036. 12506
  179037. TETRAHEDRONCVREVIEW ELECTRON TRANSFER ELECTROCYCLIZATION DIELS ALDER RADICAL CATION MECHANISM BAULDM
  179038. 13515N
  179039. 2/28/96V?CATION RADICAL CYCLOADDITIONS AND RELATED SIGMATROPIC REACTIONSW
  179040. VOL 45   1989  PG 5307a
  179041. GABRIEL WEATHERHEAD
  179042. 12507
  179043. PB    SYNTHESISCHREVIEW ZINC BROMO CONDENSATION ADDITION ORGANOMETALLIC CARBONYL FURSTNERM
  179044. 13516N
  179045. 2/28/96V+RECENT ADVANCES IN THE REFORMATSKY REACTIONW
  179046. VOL 8   1989  PG 571a
  179047. GABRIEL WEATHERHEAD
  179048. 12508
  179049. QB    GAZZ CHIMC[STEREOCHEM DIPOLAR CYCLOADDITION NITRILE OXIDE NITRONE REVIEW TRANSITION STATE DIPOLE COZZIM
  179050. 13517N
  179051. 2/28/96
  179052. QVaSTEREOCONTROL IN THE 1,3 DIPOLAR CYCLOADDITION REACTION OF NITRILE OXIDES AND NITRONES TO ALKENESW
  179053. VOL 119   1989  PG 253a
  179054. GABRIEL WEATHERHEAD
  179055. 12509
  179056. TETRAHEDRONCEAMIDINE CARBENOID EPOXIDE CARBENE REVIEW IMINE DIAZO AZOMETHINE YLIDEM
  179057. 13518N
  179058. 2/28/96V0STRUCTURE AND REACTIVITY OF CYCLOIMMONIUM YLIDESW
  179059. VOL 32   1976]   PG 2647a
  179060. GABRIEL WEATHERHEAD
  179061. 12510
  179062. ANGEW. CHEM.CUREVIEW SYNTHESIS ORGANOMETALLIC SULFONE ENANTIOSELECTIVITY MACROCYCLE MECHANISM TROSTM
  179063. 13519N
  179064. 2/28/96V8CYCLIZATIONS VIA PALLADIUM CATALYZED ALLYLIC ALKYLATIONSW
  179065. VOL 28   1989  PG 1173a
  179066. GABRIEL WEATHERHEAD
  179067. 12511
  179068. ANGEW. CHEM.CKREVIEW CYCLIZATION STEREOSELECTIVITY CYCLIC ACYCLIC VINYL MECHANISM RADICALM
  179069. 13520N
  179070. 2/28/96V$INTRAMOLECULAR FREE RADICAL REACTIONW
  179071. VOL 28   1989  PG 969a
  179072. GABRIEL WEATHERHEAD
  179073. 12512
  179074. ACC. CHEM. RES.CQREVIEW NMR SPECTROSCOPY MECHANISM PHYSICAL ORGANIC DIOXETANE DITHIANE INTERACTIONM
  179075. 13521N
  179076. 2/28/96
  179077. UVQCONFORMATIONAL ANALYSIS OF SIX MEMBERED, SULFUR CONTAINING SATURATED HETEROCYCLESW
  179078. VOL 22   1989  PG 357a
  179079. GABRIEL WEATHERHEAD
  179080. 12513
  179081. TETRAHEDRONC<REVIEW BORANE SILANE GRIGNARD REAGENT ORGANO LITHIUM ISOTOPEM
  179082. 13522N
  179083. 2/28/96VDSYNTHESIS OF RADIOLABELED COMPOUNDS VIA ORGANOMETALLIC INTERMEDIATESW
  179084. VOL 45   1989  PG 6601a
  179085. GABRIEL WEATHERHEAD
  179086. 12514
  179087. TETRAHEDRONCOREVIEW PHOSPHORUS APPLICATION SYNTHESIS REACTIVITY REACTION PHOSPHATE MARKOVSKIM
  179088. 13523N
  179089. 2/28/96V#PHOSPHO ALKYNES AND PHOSPHO ALKENESW
  179090. VOL 45   1989  PG 6019a
  179091. GABRIEL WEATHERHEAD
  179092. 12515
  179093. TETRAHEDRONCKREVIEW SULFONYL ASYMMETRIC OXIDATION AZIRIDINE HYDRAZINE NUCLEOPHILE CHIRALM
  179094. 13524N
  179095. 2/28/96V/APPLICATION OF OXAZIRIDINE IN ORGANIC SYNTHESISW
  179096. VOL 45   1989  PG 5703a
  179097. GABRIEL WEATHERHEAD
  179098. 12516
  179099. J. CHEM. SOC.CHPYRIDINIUM YLIDE DIAZO CARBENE REARRANGEMENT AMINE PYRIDINE YLIDE REVIEWM
  179100. 13525N
  179101. 2/28/96
  179102. YVHTHERMOLYSIS OF DIAZOTETRAPHENYLCYCLOPENTADIENE IN THE PRESENCE OF AMINESW
  179103. VOL 0   1971]   PG 2939a
  179104. GABRIEL WEATHERHEAD
  179105. 12517
  179106. JACSCTCARBENE CARBONYL KETONE REVIEW CARBONYL YLIDE DIAZIRINE DIPOLAR CYCLOADDITION CHLOROM
  179107. 13526N
  179108. 2/28/96VGA LASER FLASH PHOTOLYSIS STUDY OF CARBONYL YLIDES OF ARYLCHLOROCARBENESW
  179109. VOL 112   1990  PG 744a
  179110. GABRIEL WEATHERHEAD
  179111. 12518
  179112. JOCCLPYRROLIDINE WRITING INTRODUCTION REFERENCES REVIEW DIENE TOSYLAMINE BACKVALLM
  179113. 13527N
  179114. 2/28/96VFA STEREOCONTROLLED ORGANOPALLADIUM ROUTE TO DISUBSTITUTED PYRROLIDINESW
  179115. VOL 55   1990  PG 826a
  179116. GABRIEL WEATHERHEAD
  179117. 12519
  179118. JOCC:GRIGNARD REAGENT INITIATION EXPERIMENTAL REVIEW REFERENCESM
  179119. 13528N
  179120. 2/28/96VSUSE OF SOLUBLE MAGNESIUM ANTHRACENE REAGENT TO INITIATE DIFFICULT GRIGNARD REAGENTSW
  179121. VOL 55   1990  PG 788a
  179122. GABRIEL WEATHERHEAD
  179123. 12520
  179124. HETEROCYCLESC2LACTAM RING OPENING REVIEW REARRANGEMENT BETA BOSEM
  179125. 13529N
  179126. 2/28/96
  179127. ]V`CONVERSION OF BETA LACTAMS TO VERSATILE SYNTHONS VIA MOLECULAR REARRANGEMENT AND LACTAM CLEAVAGEW
  179128. VOL 27   1988  PG 1953a
  179129. GABRIEL WEATHERHEAD
  179130. 12521
  179131. PURE & APPL. CHEMISTRYC
  179132. UMPOLUNG REVIEW SYNTHON ` HOM
  179133. 13530N
  179134. 2/28/96V5CONRAPOLARIZATION A NEW CONCEPT IN ORGANIC REACTIVITYW
  179135. VOL 11   1989  PG 157a
  179136. GABRIEL WEATHERHEAD
  179137. 12522
  179138. CHEM. COMM.CLBARLUENGA DIELS ALDER SILICON SULFUR INTRAMOLECULAR HETEROCYCLE REVIEW IMINEM
  179139. 13531N
  179140. 2/28/96VfCYCLOADDITION REACTIONS OF HETERO AZADIENES. INTRAMOLECULAR DIELS ALDER REACTION OF THIA AZABUTADIENESW
  179141. VOL 0   1989  PG 1487a
  179142. GABRIEL WEATHERHEAD
  179143. 12523
  179144. TETRAHEDRONC@SYNTHESIS REVIEW CARBANION VINYL ADDITION AMINE ALKYNE CARBANIONM
  179145. 13532N
  179146. 2/28/96ViSYNTHETIC POTENTIAL OF THE TERTIARY AMINE CATALYZED REACTION OF ACTIVATED VINYL CARBANIONS WITH ALDEHYDESW
  179147. VOL 44   1988  PG 4653a
  179148. GABRIEL WEATHERHEAD
  179149. 12524
  179150. TETRAHEDRON
  179151. aCQBENZOCYCLOPROPENE AROMATICITY CARBENE SYNTHESIS BENZO REVIEW CYCLOPROPENE BILLUPSM
  179152. 13533N
  179153. 2/28/96V,METHODS FOR THE SYNTHESIS OF CYCLOPROPARENESW
  179154. VOL 44   1988  PG 1305a
  179155. GABRIEL WEATHERHEAD
  179156. 12525
  179157. bB    SYNTHESISCEREARRANGEMENT HETEROCYCLE SIGMATROPIC 3,3 REVIEW ALLENE COPE BLECHERTM
  179158. 13534N
  179159. 2/28/96V2THE HETERO COPE REARRANGEMENT IN ORGANIC SYNTHESISW
  179160. VOL 2   1989  PG 71a
  179161. GABRIEL WEATHERHEAD
  179162. 12526
  179163. PURE & APPLIED CHEMISTRYCBREVIEW INDUCTION CHIRAL ASYMMETRIC CHIRAL SULFOXIDE VINYL SOLLADIEM
  179164. 13535N
  179165. 2/28/96VHRECENT ADVANCES IN FIELD OF ASYMMETRIC SYNTHESIS USING CHIRAL SULFOXIDESW
  179166. VOL 60   1988  PG 1699a
  179167. GABRIEL WEATHERHEAD
  179168. 12527
  179169. PURE AND APPLIED CHEM.C9SYNTHESIS CYCLIZATION METAL REVIEW ENE MAGNESIUM OPPOLZERM
  179170. 13536N
  179171. 2/28/96VPMETAL DIRECTED STEREOSELECTIVE FUNCTIONALIZATION OF ALKENES IN ORGANIC SYNTHESISW
  179172. VOL 60   1990  PG 39a
  179173. GABRIEL WEATHERHEAD
  179174. 12528
  179175. HETEROCYCLES
  179176. eCATAKAHATA THIOAMIDE REVIEW HETEROCYCLE METHOD SYNTHESIS THIO AMIDEM
  179177. 13537N
  179178. 2/28/96V0SYNTHESIS OF HETEROCYCLES USING THIOAMIDE GROUPSW
  179179. VOL 27   1988  PG 1953a
  179180. GABRIEL WEATHERHEAD
  179181. 12529
  179182. PURE & APPL. CHEM.C5PALLADIUM SYNTHESIS REVIEW BIFUNCTIONAL REAGENT PIERSM
  179183. 13538N
  179184. 2/28/96V;THE USE OF SOME BIFUNCTIONAL REAGENTS JIN ORGANIC SYNTHESISW
  179185. VOL 60   1988  PG 107a
  179186. GABRIEL WEATHERHEAD
  179187. 12530
  179188. HETEROCYCLESCASATO ALKALOID REVIEW SYNTHESIS HETEROCYCLES PYRROLIZIDINE METHODSM
  179189. 13539N
  179190. 2/28/96V.RECENT ADVANCES IN SYNTHESIS OF PYRROLIZIDINESW
  179191. VOL 27   1988  PG 1465a
  179192. GABRIEL WEATHERHEAD
  179193. 12531
  179194. CHEM. REV.C@REVIEW COLUMN PIRKLE CHROMATOGRAPHY SEPARATION ENANTIOMER CHIRALM
  179195. 13540N
  179196. 2/28/96V`CONSIDERATIONS OF CHIRAL RECOGNITION RELEVANT TO LIQUID CHROMATOGRAPHY FOR ENANTIOMER SEPARATIONW
  179197. VOL 89   1989  PG 347a
  179198. GABRIEL WEATHERHEAD
  179199. 12532
  179200. CHEM. SOC. REV.C?ALKENE ANHYDRIDE AMIDE ESTER CARBONYL REVIEW WITTIG PHOSPHOROUSM
  179201. 13541N
  179202. 2/28/96
  179203. iVSWITTIG OLEFINATION REACTION WITH CARBONYL COMPOUNDS OTHER THAN ALDEHYDES OR KETONESW
  179204. VOL 17   1988  PG 1a
  179205. GABRIEL WEATHERHEAD
  179206. 12533
  179207. ANG. CHEM. INT. ED.C@LITHIUM LITHIATE STEREOCHEM REVIEW SULFONE X RAY STRUCTURE BOCHEM
  179208. 13542N
  179209. 2/28/96V2THE STRUCTURE OF THE LITHIUM COMPOUNDS OF SULFONESW
  179210. VOL 28   1989  PG 277a
  179211. GABRIEL WEATHERHEAD
  179212. 12534
  179213. CHEM. REV.CRASYMMETRIC CHIRAL EPOXIDATION TITANIUM TRANSITION METAL REVIEW PREPARATION EPOXIDEM
  179214. 13543N
  179215. 2/28/96V'TRANSITION METAL CATALYZED EPOXIDATIONSW
  179216. VOL 89   1989  PG 431a
  179217. GABRIEL WEATHERHEAD
  179218. 12535
  179219. CHEM. SOC. REV.C>RETROSYNTHESIS ANALYSIS] REVIEW SYNTHESIS RETRO TEACHING COREYM
  179220. 13544N
  179221. 2/28/96V0RETROSYNTHETIC THINKING. ESSENTIALS AND EXAMPLESW
  179222. VOL 17   1988  PG 111a
  179223. GABRIEL WEATHERHEAD
  179224. 12536
  179225. ACADEMIC PRESSCDEXPERIMENTAL LITHIATE REVIEW CARBANION LITHIUM METAL TRITRATION BOOKM
  179226. 13545N
  179227. 2/28/96V*ORGANOLITHIUM METHODS IN ORGANIC CHEMISTRYW
  179228. VOL 0   1988  PG 0
  179229. GABRIEL WEATHERHEAD
  179230. 12537
  179231. ELSEVIERC?BOOK REVIEW HIGH PRESSURE CYCLOADDITION PRESSURE THEORY LENOBLEM
  179232. 13546N
  179233. 2/28/96V
  179234. ORGANIC HIGH PRESSURE CHEMISTRYW
  179235. VOL 0   1988  PG 0a
  179236. GABRIEL WEATHERHEAD
  179237. 12538
  179238. WILEYC;HALO CHLORO ALPHA CARBONYL KETONE CHEMISTRY REVIEW DE KIMPEM
  179239. 13547N
  179240. 2/28/96V7THE CHEMISTRY OF ALPHA HALO KETONES AND RELATED SPECIESW
  179241. VOL 0   1988  PG 0a
  179242. GABRIEL WEATHERHEAD
  179243. 12539
  179244. TOPICS IN CURRENT CHEMCSTHEORY LITHIATE CARBANION REVIEW CHEMISTRY STRUCTURE PHYSICAL ORGANIC REARRANGEMENTM
  179245. 13548N
  179246. 2/28/96V
  179247. REARRANGEMENT OF CARBANIONSW
  179248. VOL 146   1988  PG 1a
  179249. GABRIEL WEATHERHEAD
  179250. 12540
  179251. TOPICS IN CURRENT CHEMISTRYC:CYCLOPROPENE CARBENE VINYL ADDITION REVIEW SYNTHESIS BAIRDM
  179252. 13549N
  179253. 2/28/96V7FUNCTIONALIZED CYCLOPROPENES AS SYNTHETIC INTERMEDIATESW
  179254. VOL 0   1988  PG 73a
  179255. GABRIEL WEATHERHEAD
  179256. 12541
  179257. TOPICS IN CURRENT CHEMISTRY
  179258. rCSREISSIG SILOXYL CYCLOPROPANE RING OPENING DESILYLATION HOMOENOLATE REVIEW CARBANIONM
  179259. 13550N
  179260. 2/28/96VXDONOR ACCEPTOR SUBSTITUTED CYCLOPROPANES. VERSATILE BUILDING BLOCKS IN ORGANIC SYNTHESISW
  179261. VOL 0   1988  PG 73a
  179262. GABRIEL WEATHERHEAD
  179263. 12542
  179264. TOPICS IN CURRENT CHEMISTRYC7METHODOLOGY REVIEW ALKYNE SYNTHESIS CYCLOPROPANE SALAUNM
  179265. 13551N
  179266. 2/28/96VqSYNTHESIS AND SYNTHETIC APPLICATIONS OF 1 DONOR SUBSTITUTED CYCLOPROPANES WITH ETHYNYL, VINYL AND CARBONYL GROUPSW
  179267. VOL 3   1988  PG 1a
  179268. GABRIEL WEATHERHEAD
  179269. 12543
  179270. CHEM. REV.C&CYCLOPROPANE REVIEW SYNTHESIS HUDLICKYM
  179271. 13552N
  179272. 2/28/96V7USE OF CYCLOPROPANES AND THEIR USE IN ORGANIC SYNTHESISW
  179273. VOL 89   1989  PG 165a
  179274. GABRIEL WEATHERHEAD
  179275. 12544
  179276. ADV. PHYS. ORG. CHEM.CAPRINCIPLE STEREOELECTRONIC STEREOCHEM REVIEW LEAST MOTION SINNOTTM
  179277. 13553N
  179278. 2/28/96VBTHE PRINCIPLE OF LEAST NUCLEAR MOTION AND STEREOELECTRONIC CONTROLW
  179279. VOL 24   1988  PG 113a
  179280. GABRIEL WEATHERHEAD
  179281. 12545
  179282. vCHUNSATURATED RHODIUM KETONE DIAZO INSERTION REVIEW CYCLOPENTENONE WENKERTM
  179283. 13554N
  179284. 2/28/96VsA GENERAL CYCLOPENTENONE SYNTHESIS INVOLVING A RHODIUM (II) INTRAMOLECULAR CARBON HYDROGEN INSERTIONOF DIAZOKETONESW
  179285. VOL 55   1990  PG 811a
  179286. GABRIEL WEATHERHEAD
  179287. 12546
  179288. JOCCSPHYSICAL ORGANIC COMPUTER CYCLIZATION BIMOLECULAR ADDITION REVIEW RADICAL JORGENSONM
  179289. 13555N
  179290. 2/28/96V-KEY ASPECTS OF ORGANIC FREE RADICAL CHEMISTRYW
  179291. VOL 55   1990  PG 10a
  179292. GABRIEL WEATHERHEAD
  179293. 12547
  179294. Tet. Lett.C=ASYMMETRIC CHIRAL STEREOCHEM ALDOL BORON BORINATE ENOL REVIEWM
  179295. 13556N
  179296. 2/28/96V+REVIEW ON ALDOL CHEMISTRY OF ENOL BORINATESW
  179297. VOL 0   1989  PG 7121a
  179298. GABRIEL WEATHERHEAD
  179299. 12548
  179300. JOCCIRHODIUM REFERENCES REVIEW WRITING SYNTHESIS CARBENOID INTRODUCTION COPPERM
  179301. 13557N
  179302. 2/28/96VAGENERATION AND REACTIONS OF NOVEL COPPER CARBENOIDS FOR SYNTHESISW
  179303. VOL 55   1990  PG 329a
  179304. GABRIEL WEATHERHEAD
  179305. 12549
  179306. CHEMTRACTS
  179307. zCLSYNTHESIS CARBOHYDRATE CARBONYL CHIRAL REVIEW DANISHEFSKY REVIEW DIELS ALDERM
  179308. 13558N
  179309. 2/28/96VqCYCLOADDITION AND CYCLOCONDENSATION REACTIONS OF HIGHLY FUNCTIONALIZED DIENES.  APPLICATIONS TO ORGANIC SYNTHESISW
  179310. VOL 2   1989  PG 273a
  179311. GABRIEL WEATHERHEAD
  179312. 12550
  179313. JACSCUSYNTHESIS REFERENCE WRITING DIPOLE DIPOLAR CYCLOADDITION REVIEW CARBONYL YLIDE WENDERM
  179314. 13559N
  179315. 2/28/96VNSYNTHESIS OF PHORBOL ESTER BY A PYRYLINN ION ALKENE CYCLOADDITION   SEE REF 12W
  179316. VOL 111   1989  PG 8954a
  179317. GABRIEL WEATHERHEAD
  179318. 12551
  179319. ACC. CHEM. RESEARCHCINITRENE 2,3 SIGMATROPIC REARRANGEMENT STEVENS REVIEW DIAZO SULFONIUM ANDOM
  179320. 13560N
  179321. 2/28/96V\YLIDE FORMATION AND REARRANGEMMENT IN THE REACTION OF CARBENE WITH DIVALENT SULFUR COMPOUNDSW
  179322. VOL 10   1977]   PG 179a
  179323. GABRIEL WEATHERHEAD
  179324. 12552
  179325. TETREDRON LETT.C?REVIEW EPOXIDE DIAZO PHOTOLYSIS YLIDE OXONIUM CARBENOID NOZAZKIM
  179326. 13561N
  179327. 2/28/96V5THE REACTION OF ETHYL DIAZOACETATE WITH STYRENE OXIDEW
  179328. VOL 30   1965]   PG 2563
  179329. GABRIEL WEATHERHEAD
  179330. 12553
  179331. ANGEW. CHEM. INT. ED. ENGL.C>BOCHE REVIEW DITHIANE LITHIATE ANION DIANION SULFONE CARBANIONM
  179332. 13562N
  179333. 2/28/96VULITHIUM STRUCTURE OF SULFONES, SULFOXIDES, THIOETHERS, NITRILES, NITRO AND HYDRAZONESW
  179334. VOL 28   1989  PG 277a
  179335. GABRIEL WEATHERHEAD
  179336. 12554
  179337. JACSC9NUGENT EPOXIDE ACRYLATE METAL LACTONE REVIEW RING OPENINGM
  179338. 13563N
  179339. 2/28/96VUBIMOLECULAR ADDITION OF EPOXIDES TO ACTIVATED OLEFINS A NEW REACTION TO MAKE LACTONESW
  179340. VOL 111   1989  PG 4525a
  179341. GABRIEL WEATHERHEAD
  179342. 12555
  179343. Tet. Lett.CIREVIEW KETONE ENOL ENOLATE MECHANISM STEREOSELECTIVITY STEREOCHEM POLLACKM
  179344. 13564N
  179345. 2/28/96VISTEREOELECTRONIC CONTROL IN THE REACTIONS OF KETONES AND THEIR ENOL(ATE)SW
  179346. VOL 45   1989  PG 4913a
  179347. GABRIEL WEATHERHEAD
  179348. 12556
  179349. TETRAHEDRONCKREVIEW CATION RADICAL CYCLOADDITION SIGMATROPIC DIELS ALDER MECHANISM BAULDM
  179350. 13565N
  179351. 2/28/96V>CATION RADICAL CYCLOADDITION AND RELATED SIGMATROPIC REACTIONSW
  179352. VOL 45   1989  PG 5307
  179353. GABRIEL WEATHERHEAD
  179354. 12557
  179355. TETRAHEDRONC@BOYKIN REVIEW NMR SPECTROSCOPY STRUCTURE ORGANIC COMPOUND OXYGENM
  179356. 13566N
  179357. 2/28/96VU17O NMR SPECTROSCOPY: ASSESSMENT OF STERIC PERTURBATION OF STRUCTURE IN ORG. COMPONDSW
  179358. VOL 45   1989  PG 3613a
  179359. GABRIEL WEATHERHEAD
  179360. 12558
  179361. TETRAHEDRONCKBERNASCONI REVIEW OLEFIN NUCLEOPHILIC ADDITION KINETICS MECHANISM CHEMISTRYM
  179362. 13567N
  179363. 2/28/96V8NUCLEOPHILIC ADDITION TO OLEFINS. KINETICS AND MECHANISMW
  179364. VOL 45   1989  PG 4017a
  179365. GABRIEL WEATHERHEAD
  179366. 12559
  179367. TETRAHEDRONCBMCDONALD REVIEW CARBENE ANION RADICAL GENERATION CHEMISTRY THERMALM
  179368. 13568N
  179369. 2/28/96VCGENERATION, THERMOCHEMISTRY AND CHEMISTRY OF CARBENE ANION RADICALSW
  179370. VOL 45   1989  PG 3993a
  179371. GABRIEL WEATHERHEAD
  179372. 12560
  179373. TETRAHEDRONCIMORI REVIEW SYNTHESIS ASYMMETRIC NATURAL PRODUCT CHIRAL PHEROMONES TARGETM
  179374. 13569N
  179375. 2/28/96V&SYNTHESIS OF OPTICAL ACTIVE PHEROMONESW
  179376. VOL 45   1989  PG 3233a
  179377. GABRIEL WEATHERHEAD
  179378. 12561
  179379. ACCOUNTS OF CHEMICAL RESEARCHC9TURRO REVIEW RADICAL TRIPLET PHOTOCHEM MECHANISM REACTIONM
  179380. 13570N
  179381. 2/28/96V'DYNAMICS OF FLEXIBLE TRIPLET BIRADICALSW
  179382. VOL 22   1989  PG 199a
  179383. GABRIEL WEATHERHEAD
  179384. 12562
  179385. ACCOUNTS OF CHEMICAL RESEARCHC;PERRIN REVIEW AMIDE MECHANISM CHEMISTRY NMR EXCHANGE PROTONM
  179386. 13571N
  179387. 2/28/96V8PROTON EXCHANGE IN AMIDES: SURPRISES FROM SIMPLE SYSTEMSW
  179388. VOL 22   1989  PG 268a
  179389. GABRIEL WEATHERHEAD
  179390. 12563
  179391. ACCOUNTS OF CHEMICAL RESEARCHCKBIEHL REVIEW SYNTHESIS HETEROCYCLE ARYLATION BENZYNE ANNULATION CYCLIZATIONM
  179392. 13572N
  179393. 2/28/96V6SYNTHESIS OF POLYCYCLICS VIA ARYNE ARYLATION REACTIONSW
  179394. VOL 22   1989  PG 275a
  179395. GABRIEL WEATHERHEAD
  179396. 12564
  179397. ACCOUNTS OF CHEMICAL RESEARCHCAADAM REVIEW REAGENT OXIDATION KETONE REACTIVITY MECHANISM OXIRANEM
  179398. 13573N
  179399. 2/28/96V,DIOXIRANES: A NEW CLASS OF POWERFUL OXIDANTSW
  179400. VOL 22   1989  PG 205a
  179401. GABRIEL WEATHERHEAD
  179402. 12565
  179403. CISCHLEYER REVIEW INTRODUCTION ORTHO LITHIATION CHELATION WRITING MO THEORYM
  179404. 13574N
  179405. 2/28/96V2MECHANISTIC EVIDENCE FOR ORTHO DIRECTED LITHIATIONW
  179406. VOL 111   1989  PG 7191a
  179407. GABRIEL WEATHERHEAD
  179408. 12566
  179409. ACC. CHEM. RES.C@BIEHL REVIEW ARYNE CYCLIZATION TARGET SYNTHESIS BENZENE ALKALOIDM
  179410. 13575N
  179411. 2/28/96VLANNULATIONS INVOLVING ARYNE SIDE CHAIN CYCLIZATIONS SYNTHESIS OF POLYCYCLICSW
  179412. VOL 22   1989  PG 275a
  179413. GABRIEL WEATHERHEAD
  179414. 12567
  179415. JOCCNINTRODUCTION WRITING SPIRO ALKALOID SYNTHESIS REVIEW PERHYDRO HISTRIONICOTOXINM
  179416. 13576N
  179417. 2/28/96V
  179418. PERHYDRO HISTRIONICOTOXINW
  179419. VOL 54   1989  PG 4419a
  179420. GABRIEL WEATHERHEAD
  179421. 12568
  179422. JACSCCNELSON BICYCLIC AMINE NMR INVERSION NITROGEN REVIEW BICYCLIC EFFECTM
  179423. 13577N
  179424. 2/28/96VKNITROGEN INVERSION BARRIER TO BICYCLIC AMINES AND ENERGY OF FREE ACTIVATIONW
  179425. VOL 111   1989  PG 1776a
  179426. GABRIEL WEATHERHEAD
  179427. 12569
  179428. JOCCDTANNER REVIEW ALKALOID PERHYDRO HISTRIONICOTOXIN EPOXY KETONE TARGETM
  179429. 13578N
  179430. 2/28/96
  179431. VGA STEREOSELECTIVE ORGANOPALLADIUM ROUTE TOWARD PERHYDROHISTRIONICOTOXINW
  179432. VOL 54   1989  PG 3374a
  179433. GABRIEL WEATHERHEAD
  179434. 12570
  179435. B    SYNTHESISC:ROSINI CARBANION REVIEW NITRO SYNTHON SYNTHESIS ALKYLATIONM
  179436. 13579N
  179437. 2/28/96VGFUNCTIONALIZED NITROALKANES AS USEFUL REAGENTS FOR ALKYL ANION SYNTHONSW
  179438. VOL 11   1989  PG 833a
  179439. GABRIEL WEATHERHEAD
  179440. 12571
  179441. ANGEW CHEM INT ED ENGLCFHEGEDUS REVIEW PALLADIUM CYCLIZATION INDOLE ORTHO ORGANOMETALLIC METALM
  179442. 13580N
  179443. 2/28/96V?TRANSITION METALS IN SYNTHESIS AND FUNCTIONALIZATION OF INDOLESW
  179444. VOL 27   1989  PG 1113a
  179445. GABRIEL WEATHERHEAD
  179446. 12572
  179447. B    SYNTHESISC?SCHINZER ALLYL SILYL PROPARGYL SAKURAI ANNELATION REVIEW SILANEM
  179448. 13581N
  179449. 2/28/96VDINTRAMOLECULAR ADDITION REACTIONS OF ALLYLIC AND PROPARGYLIC SILANESW
  179450. VOL 0   1988  PG 263a
  179451. GABRIEL WEATHERHEAD
  179452. 12573
  179453. TETRAHEDRONC;MATTESON BORON REVIEW ESTER CHIRAL STEREOCHEM HYDROBORATIONM
  179454. 13582N
  179455. 2/28/96V*BORONIC ESTERS IN STEREODIRECTED SYNTHESIS
  179456. VOL 45   1989  PG 1859a
  179457. GABRIEL WEATHERHEAD
  179458. 12574
  179459. JOCC=YUS SULFONE VINYL REVIEW CARBANION ADDITION CARBONYL ALKOXIDEM
  179460. 13583N
  179461. 2/28/96VSSUBSTITUTED LITHIUM TOSYL PROPENOLATES AS USEFUL INTERMEDIATES IN ORGANIC SYNTHESISW
  179462. VOL 54   1989  PG 1491a
  179463. GABRIEL WEATHERHEAD
  179464. 12575
  179465. JACSCEGAWLEY OXAZOLINE CHIRAL LITHIUM LITHIATE REVIEW ALKYLATION ASYMMETRICM
  179466. 13584N
  179467. 2/28/96VoCHIRAL DIPOLE STABILIZED ANIONS STEREOSELECTIVE DEPROTONATION AND SELECTIVE ALKYLATIONS OF LITHIATED OXAZOLINESW
  179468. VOL 111   1989  PG 2211a
  179469. GABRIEL WEATHERHEAD
  179470. 12576
  179471. ACC CHEM RESCMWONG DEOXYGENATION TITANIUM REVIEW ISOBENZOFURAN ALKYNE ACETYLENE DIELS ALDERM
  179472. 13585N
  179473. 2/28/96VKSYNTHESIS OF NOVEL BENZENOID MOLECULES BY LOW VALENT TITANIUM DEOXYGENATIONW
  179474. VOL 22   1989  PG 145a
  179475. GABRIEL WEATHERHEAD
  179476. 12577
  179477. ACC CHEM RESCKCOHEN LITHIATE SULFUR THIO THIOPHENYL ELECTRON TRANSFER CYCLOPROPANE REVIEWM
  179478. 13586N
  179479. 2/28/96
  179480. V?RADICAL ANION INDUCED REDUCTIVE ALKYLATION OF PHENYL THIOETHERSW
  179481. VOL 22   1989  PG 152a
  179482. GABRIEL WEATHERHEAD
  179483. 12578
  179484. ANGEW CHEM INTERNAT EDITC3VIEHE YNAMINE REVIEW AMINO ALKYNE AMINE PREPARATIONM
  179485. 13587N
  179486. 2/28/96V(SYNTHESIS AND REACTIONS OF ALKYNYLAMINESW
  179487. VOL 6   1967]   PG 767a
  179488. GABRIEL WEATHERHEAD
  179489. 12579
  179490. CHEMTRACTS ORG CHEMC6TROST REVIEW TRANSITION METAL CATALYST PALLADIUM METALM
  179491. 13588N
  179492. 2/28/96V@REVIEW OF TRANSITION METAL CATALYZED SELECTIVE ORGANIC REACTIONSW
  179493. VOL 1   1988  PG 415a
  179494. GABRIEL WEATHERHEAD
  179495. 12580
  179496. HETEROCYCLESCOLUKEVICS REVIEW SONICATION HETEROCYCLE SOUND ALKYLATION REDUCTION CYCLOADDITIONM
  179497. 13589N
  179498. 2/28/96V
  179499. HETEROCYCLIC SONOCHEMISTRYW
  179500. VOL 29   1989  PG 597a
  179501. GABRIEL WEATHERHEAD
  179502. 12581
  179503. CHEM REVCGSCHORE REVIEW CYCLOADDITION METAL TRANSITION CATALYZED ALKYNE SYNTHESISM
  179504. 13590N
  179505. 2/28/96VQTRANSITION METAL MEDIATED CYCLOADDITION REACTIONS OF ALKYNES IN ORGANIC SYNTHESISW
  179506. VOL 88   1988  PG 1081
  179507. GABRIEL WEATHERHEAD
  179508. 12582
  179509. CHEM REVCEOJIMA REVIEW METAL TRANSITION CATALYZED CARBONYLATION CARBON MONOXIDEM
  179510. 13591N
  179511. 2/28/96VNNEW ASPECTS OF CARBONYLATION REACTIONS CATALYZED BY TRANSITION METAL COMPLEXESW
  179512. VOL 88   1988  PG 1011a
  179513. GABRIEL WEATHERHEAD
  179514. 12583
  179515. ACCOUNT CHEM RESEARCHCIWAGNER PHOTOCHEM HYDROGEN ABSTRACTION REVIEW KETONE DELTA NORRISH TYPE IIM
  179516. 13592N
  179517. 2/28/96Vf1,5 BIRADICALS AND FIVE MEMBERED RINGS GENERATED BY DELTA HYDROGEN ABSTRACTION IN PHOTOEXCITED KETONESW
  179518. VOL 22   1989  PG 83a
  179519. GABRIEL WEATHERHEAD
  179520. 12584
  179521. CHEM REVC@ZIEGLER REVIEW THERMAL REARRANGEMENT CLAISEN ALIPHATIC SYNTHESISM
  179522. 13593N
  179523. 2/28/96V+THE THERMAL ALIPHATIC CLAISEN REARRANGEMENTW
  179524. VOL 88   1988  PG 1423a
  179525. GABRIEL WEATHERHEAD
  179526. 12585
  179527. CHEM REVC@CRIMMINS REVIEW PHOTOCHEM INTRAMOLECULAR CYCLOADDITION ENONE 2+2M
  179528. 13594N
  179529. 2/28/96VISYNTHETIC APPLICATIONS OF INTRAMOLECULAR ENONE OLEFIN PHOTOCYCLOADDITIONSW
  179530. VOL 88   1988  PG 1453a
  179531. GABRIEL WEATHERHEAD
  179532. 12586
  179533. HETEROCYCLESCBTAKAHATA HETEROCYCLIC THIOAMIDE SULFUR SYNTHESIS REVIEW THIO AMIDEM
  179534. 13595N
  179535. 2/28/96V0SYNTHESIS OF HETEROCYCLES USING THIOAMIDE GROUPSW
  179536. VOL 27   1988  PG 1953a
  179537. GABRIEL WEATHERHEAD
  179538. 12587
  179539. TOP CURR CHEMCJSHONO REVIEW ELECTROCHEM ALKALOID SYNTHESIS ELECTROLYSIS ELECTRON TRANSFERM
  179540. 13596N
  179541. 2/28/96VQSYNTHESIS OF ALKALOIDAL COMPOUNDS USING AN ELECTROCHEMICAL REACTION AS A KEY STEPW
  179542. VOL 148   1988  PG 131a
  179543. GABRIEL WEATHERHEAD
  179544. 12588
  179545. CHEM REVC;WONG CYCLOPROPANE REVIEW SYNTHESIS SMALL RING STRAIN TARGETM
  179546. 13597N
  179547. 2/28/96V?USE OF CYCLOPROPANES AND THEIR DERIVATIVES IN ORGANIC SYNTHESISW
  179548. VOL 89   1989  PG 165a
  179549. GABRIEL WEATHERHEAD
  179550. 12589
  179551. ANGEW. CHEM. INT.C
  179552. AUTHORS = TROST,BM  TOPICS =  TROST; TROST REVIEW; ALLYLIC ALKYLATION; PALLADIUM CATALYZED;  PI ALLYL PALLADIUM; ALLYLPALLADIUM; ALLYL PALLADIUM;  PI ALLYLPALLADIUMM
  179553. 13598N
  179554. 2/28/96V8CYCLIZATIONS VIA PALLADIUM CATALYZED ALLYLIC ALKYLATIONS
  179555. W%VOL = 28/9     YEAR = 1989  PP = 1173a
  179556. GABRIEL WEATHERHEAD
  179557. 12590
  179558. TET. LETT.CnAUTHORS = MOODY,CJ; BECK,AL; COATES,WJ  TOPICS = ERGOT ALKALOIDS; INDOLE; INDOLOQUINONE; ERGOT ALKALOID REVIEWM
  179559. 13599N
  179560. 2/28/96V:PREPARATION OF TETRAHYDROBENZ[CD]INDOLES FROM 1 TETRALONESW
  179561. VOL = 30  YR = 1989  PP = 4017a
  179562. GABRIEL WEATHERHEAD
  179563. 12591
  179564. TETRAHEDRONC
  179565. AUTHORS = DAVID,S; HANNESSIAN,S  TOPICS = TIN; ORGANOTIN; ORGANOTIN ALKOXIDE; TIN REVIEW; ORGANOTIN REVIEW;  TIN ALKOXIDE; TIN OXYGENM
  179566. 13600N
  179567. 2/28/96VPORGANOTIN ALKOXIDE REVIEW. INCREASED NUCLEOPHILICITY WITHOUT INCREASED BASICITY.W
  179568. VOL = 41  YR = 1985  PP = 643a
  179569. GABRIEL WEATHERHEAD
  179570. 12592
  179571. CHEM. REV.C^AUTHORS = ZIEGLER,FE  TOPICS = ZIEGLER; CLAISEN; CLAISEN REARRANGEMENT; REVIEW; CLAISEN REVIEWM
  179572. 13601N
  179573. 2/28/96V,THE THERMAL, ALIPHATIC CLAISEN REARRANGEMENTW
  179574. VOL = 88  YR = 1988  PP = 1423a
  179575. GABRIEL WEATHERHEAD
  179576. 12593
  179577. HETEROCYCLES
  179578. C@ACETAMIDE HETEROCYCLE CYANO THIO SYNTHESIS REVIEW PYRROLE INDOLEM
  179579. 13602N
  179580. 2/28/96V4 UTILITY OF CYANOACETAMIDE IN HETEROCYCLIC SYNTHESISW
  179581. VOL 24   1986  PG 2023a
  179582. GABRIEL WEATHERHEAD
  179583. 12594
  179584. B    SYNTHESISC'REVIEW DBN DBU ELIMINATION BASE REAGENTM
  179585. 13603N
  179586. 2/28/96V! A REVIEW OF DBN AND DBU REAGENTSW
  179587. VOL 0   1972  PG 591a
  179588. GABRIEL WEATHERHEAD
  179589. 12595
  179590. ANGEW. CHEM. INT. ED. ENGL.,C'REVIEW CARBANION HMPA CHELATION REAGENTM
  179591. 13604N
  179592. 2/28/96V
  179593.  REVIEW OF HMPAW
  179594. VOL 6   YR[67]   PG 1046a
  179595. GABRIEL WEATHERHEAD
  179596. 12596
  179597. ANG. CHEM. INT. ED. ENGLCOTROST REVIEW [3+2] CYCLOADDITION ORGANOMETALLIC CYCLOPENTANE CARBOCYCLE SILICONM
  179598. 13605N
  179599. 2/28/96VV [3+2] CYCLOADDITION APPROACH TO 5 MEMBERED RINGS VIA TRIMETHYLENE AND ITS EQUIVALENTSW
  179600. VOL 25   1986  PG 1a
  179601. GABRIEL WEATHERHEAD
  179602. 12597
  179603. HETEROCYCLESC?KABALKA PYRROLE ALKENE NITRONE OXAZOLE REVIEW NITRO HETEROCYCLEM
  179604. 13606N
  179605. 2/28/96V. NITROALKENES IN THE SYNTHESIS OF HETEROCYCLESW
  179606. VOL 24   1986  PG 2645
  179607. GABRIEL WEATHERHEAD
  179608. 12598
  179609. ANGCJSTILLE REVIEW COUPLING CATALYZED PALLADIUM ELECTROPHILE TIN ORGANOMETALLICM
  179610. 13607N
  179611. 2/28/96Vb THE PALLADIUM CATALYZED CROSS COUPLING REACTIONS OF ORGANOTIN REAGENTS WITH ORGANIC ELECTROPHILESW
  179612. VOL 25   1986  PG 508a
  179613. GABRIEL WEATHERHEAD
  179614. 12599
  179615. TET LETTCLMANN CHRYSANTHEMIC ACID INSECTISIDE CYCLOPROPANE CARBOXYLIC SYNTHESIS REVIEWM
  179616. 13608N
  179617. 2/28/96V& NOVEL APPROACH TO CHRYSANTHEMIC ACIDSW
  179618. VOL 0   1986  PG 3533a
  179619. GABRIEL WEATHERHEAD
  179620. 12600
  179621. JACSCZCHIRAL INDUCTION DIPOLAR CYCLOADDITION ASYMMETRIC NITRONE DIASTEREOSELECTIVE DIPOLE REVIEWM
  179622. 13609N
  179623. 2/28/96V; ASYMMETRIC 1,3  DIPOLAR CYCLOADDITION REACTION OF NITRONESW
  179624. VOL 108   1986  PG 4647a
  179625. GABRIEL WEATHERHEAD
  179626. 12601
  179627. B    SYNTHESISCHOLAH NATION H ALKYLATION POLYMERIZATION SYNTHESIS POLYMER REAGENT REVIEWM
  179628. 13610N
  179629. 2/28/96V' POLYMERS IN ORGANIC SYNTHESIS (REVIEW)W
  179630. VOL 7   1986  PG 513a
  179631. GABRIEL WEATHERHEAD
  179632. 12602
  179633. TET LETT
  179634. CBSTREITH HETERO COPE HYDROXYL AMINE CLEAVAGE NITROGEN OXYGEN REVIEWM
  179635. 13611N
  179636. 2/28/96VE HETEROCOPE REARRANGEMENTS OF N PHENYL VINYLHYDROXYLAMINE DERIVATIVESW
  179637. VOL 0   1986  PG 3138a
  179638. GABRIEL WEATHERHEAD
  179639. 12603
  179640. TET LETTCFSOLLHUBER ULTRASOUND REVIEW REFERENCE STRECKER CYANO AMINE METHODOLOGYM
  179641. 13612N
  179642. 2/28/96V' APPLICATION OF ULTRASOUND IN SYNTHESISW
  179643. VOL 0   1986  PG 3285a
  179644. GABRIEL WEATHERHEAD
  179645. 12604
  179646. B    CHEM COMMCCATKINSON CHIRAL ASYMMETRIC NITRENE AZIRIDINE INDUCTION AMINO REVIEWM
  179647. 13613N
  179648. 2/28/96V  CHIRAL AZIRIDINATION OF ALKENESW
  179649. VOL 0   1986  PG 832a
  179650. GABRIEL WEATHERHEAD
  179651. 12605
  179652. JACSCYHUDLICKY ALKALOID PYROLIZIDINE REVIEW AZIDE INTRAMOLECULAR DIPOLAR CYCLOADDITION NITROGENM
  179653. 13614N
  179654. 2/28/96VX REVIEW OF PYROLIZIDINE ALKALOID SYNTHESIS USING THE INTRAMOLECULAR PYRROLINE ANNULATIONW
  179655. VOL 108   1986  PG 3755a
  179656. GABRIEL WEATHERHEAD
  179657. 12606
  179658. JOCCAMARYANOFF ACYL IMINIUM ION ALKALOID CYCLIZATION REVIEW STEREOCHEMM
  179659. 13615N
  179660. 2/28/96
  179661. VN REVIEW OF N ACYLIMINIUM ION CYCLIZATIONS AND STEREOSELECTIVITY OF THE PROCESSW
  179662. VOL 51   1986  PG 1341a
  179663. GABRIEL WEATHERHEAD
  179664. 12607
  179665. JACSC6PORTER RADICAL CYCLIZATION MACRO LARGE RING TIN REVIEWM
  179666. 13616N
  179667. 2/28/96V
  179668.  FREE RADICAL MACROCYCLIZATIONW
  179669. VOL 108   1986  PG 2787a
  179670. GABRIEL WEATHERHEAD
  179671. 12608
  179672. JACSCBHOUK GAUSIAN THEORY MO CALCULATIONS STO 3G PHYSICAL ORGANIC REVIEWM
  179673. 13617N
  179674. 2/28/96VB USE OF STO 3G BASIS SET GAUSIAN CALCULATIONS IN ORGANIC CHEMISTRYW
  179675. VOL 108   1986  PG 2659a
  179676. GABRIEL WEATHERHEAD
  179677. 12609
  179678. TET LETTCCHOLTON VINYL CARBANION SULFUR ENOLATE CYCLIZATION ANNULATION REVIEWM
  179679. 13618N
  179680. 2/28/96V) A NEW STEREOSPECIFIC ANNULATION REACTIONW
  179681. VOL 0   1986  PG 2087a
  179682. GABRIEL WEATHERHEAD
  179683. 12610
  179684. JOCC6BUYNAK ALLENE CYCLOADDITION REVIEW PREPARATION SULFONEM
  179685. 13619N
  179686. 2/28/96V- CYCLOADDITION REACTION OF ALLENES   A REVIEWW
  179687. VOL 51   1986  PG 1571a
  179688. GABRIEL WEATHERHEAD
  179689. 12611
  179690. C<KRAUS ENONE BRIDGED PROCEDURE REVIEW ALKENE STRAIN SYNTHESISM
  179691. 13620N
  179692. 2/28/96V
  179693.  SYNTHESIS OF BRIDGEHEAD ENONESW
  179694. VOL 1   1985  PG 116a
  179695. GABRIEL WEATHERHEAD
  179696. 12612
  179697. JOCCHEGUCHI THIO CARBONYL REVIEW WRITING CYCLOADDITION INTRODUCTION REFERENCEM
  179698. 13621N
  179699. 2/28/96V: THERMAL CYCLOADDITION REACTIONS OF THIOCARBONYL COMPOUNDSW
  179700. VOL 51   1986  PG 314a
  179701. GABRIEL WEATHERHEAD
  179702. 12613
  179703. B    SYNTHESISCGMATSUMOTO HIGH PRESSURE REACTION ORGANIC SYNTHESIS REVIEW HIGH PRESSUREM
  179704. 13622N
  179705. 2/28/96V& ORGANIC SYNTHESIS UNDER HIGH PRESSUREW
  179706. VOL 0   1985  PG 999a
  179707. GABRIEL WEATHERHEAD
  179708. 12614
  179709. ACC CHEM RESC2SCHMIDBAUR REVIEW YLIDE SILICON PHOSPHOROUS SULFURM
  179710. 13623N
  179711. 2/28/96V
  179712. SILICON YLIDE CHEMISTRYW
  179713. VOL 8   1975  PG 62a
  179714. GABRIEL WEATHERHEAD
  179715. 12615
  179716. JACSC<CHAPMAN WOLFF REARRANGEMENT DIAZO REVIEW KETONE CARBENE KETOM
  179717. 13624N
  179718. 2/28/96V.MECHANISM AND STUDY OF THE WOIFF REARRANGEMENTW
  179719. VOL 107   1985  PG 7597a
  179720. GABRIEL WEATHERHEAD
  179721. 12616
  179722. CASNIDER ENE REACTION MECHANISM REVIEW ISOTOPE DEUTERIUM LEWIS ACIDM
  179723. 13625N
  179724. 2/28/96V3MECHANISM OF THE LEWIS ACID CAT6ALYZED ENE REACTIONW
  179725. VOL 107   1985  PG 8160a
  179726. GABRIEL WEATHERHEAD
  179727. 12617
  179728. ALDR. CHEM ACTACLMEYERS FORMAMIDINE CHELATION LITHIATE CARBANION ALKYLATION ASYMMETRIC REVIEWM
  179729. 13626N
  179730. 2/28/96V`FORMAMIDINES AS PRECURSORS TO ALPHA AMINO CARBANIONS AND THEIR APPLICATION TO ASYMMETRIC SYNTHESW
  179731. VOL 18   1985  PG 59a
  179732. GABRIEL WEATHERHEAD
  179733. 12618
  179734. J HET CHEMCHGHOSEZ AZA DIENE DIELS ALDER INTRAMOLECULAR REVIEW AZIRINE CYCLOADDITIONM
  179735. 13627N
  179736. 2/28/96VGUSE OF AZADIENES IN THE DIELS ALDER REACTION FOR HETEROCYCLIC SYNTHESISW
  179737. VOL 69   1985  PG 0a
  179738. GABRIEL WEATHERHEAD
  179739. 12619
  179740. JACSC<SCHLEYER ANOMERIC EFFECT THEORY WRITING INTRODUCTION STUDENTM
  179741. 13628N
  179742. 2/28/96V%ANOMERIC EFFECTS   REFERENCE & REVIEWW
  179743. VOL 107   1985  PG 6393a
  179744. GABRIEL WEATHERHEAD
  179745. 12620
  179746. JACSCHJOHNSON RADICAL CATION WRITING REVIEW PHOTOCHEM ALLENE ELECTRON TRANSFER
  179747. 13629N
  179748. 2/28/96V+SOLUTION PHASE CHEMISTRY OF RADICAL CATIONSW
  179749. VOL 107   1985  PG 6615a
  179750. GABRIEL WEATHERHEAD
  179751. 12621
  179752. BULL SOC CHIM FRC6QUANG REVIEW DIPOLAR CYCLOADDITION ALLENE DIAZO DIPOLEM
  179753. 13630N
  179754. 2/28/96V2DIPOLAR CYCLOADDITIONS WITH MONOFUNCTIONAL ALLENESW
  179755. VOL 0   1978  PG 401a
  179756. GABRIEL WEATHERHEAD
  179757. 12622
  179758. TETRAHEDRONC?PASTO ALLENE REVIEW DIPOLAR CYCLOADDITION REVIEW WRITING THEORYM
  179759. 13631N
  179760. 2/28/96V'RECENT DEVELOPMENTS IN ALLENE CHEMISTRYW
  179761. VOL 0   1984  PG 2805a
  179762. GABRIEL WEATHERHEAD
  179763. 12623
  179764. ACC CHEM RESC<YOSHIKOSHI NITRO ALKENE CONJUGATE ADDITION REVIEW SILYL ENOLM
  179765. 13632N
  179766. 2/28/96VAOXYALKYLATION OF CARBONYL COMPOUNDS WITH CONJUGATED NITRO OLEFINSW
  179767. VOL 18   1985  PG 284a
  179768. GABRIEL WEATHERHEAD
  179769. 12624
  179770. TET LETTCDPINTO ANOMERIC WRITING EFFECT SULFUR REFERENCE REVIEW CONFORMATIONALM
  179771. 13633N
  179772. 2/28/96V ANOMORIC EFFECT IN 1,3 DITHIANESW
  179773. VOL 0   1985  PG 5235a
  179774. GABRIEL WEATHERHEAD
  179775. 12625
  179776. CFANDERSON ENE INTRAMOLECULAR LEWIS ACID ALDEHYDE REVIEW SYNTHESIS PRINSM
  179777. 13634N
  179778. 2/28/96V/INTRAMOLECULAR ENE REACTION OF OLEFIN ALDEHYDESW
  179779. VOL 50   1985  PG 4144a
  179780. GABRIEL WEATHERHEAD
  179781. 12626
  179782. ACCT CHEM RES.18CLHOFFMAN NORBORNADIENE THERMAL REARRANGEMENT EXTRUSION REVIEW CARBENE METHOXYM
  179783. 13635N
  179784. 2/28/96V+THERMOLYSIS OF 7 SUBSTITUTED NORBORNADIENESW
  179785. VOL 0   1985  PG 248a
  179786. GABRIEL WEATHERHEAD
  179787. 12627
  179788. CHEM REVC%BURWELL ETHER CLEAVAGE REVIEW REAGENTM
  179789. 13636N
  179790. 2/28/96V
  179791. CLEAVAGE OF ETHERSW
  179792. VOL 54   YR[54]   PG 615a
  179793. GABRIEL WEATHERHEAD
  179794. 12628
  179795. B    SYNTHESISC:REGITZ REVIEW DIAZO DIAZOALKANE ELECTROPHILIC SUBSTITUTIONM
  179796. 13637N
  179797. 2/28/96V&ELECTROPHILIC DIAZOALKANE SUBSTITUTIONW
  179798. VOL 0   1985  PG 569a
  179799. GABRIEL WEATHERHEAD
  179800. 12629
  179801. HETEROCYCLESC1KURASAWA REVIEW HETEROCYCLE SYNTHESIS QUINOXALINEM
  179802. 13638N
  179803. 2/28/96V
  179804. RECENT PROGRESS IN THE QUINOXALINE CHEMISTRY:UTILITY OF 3 ALKOXY CARBONYLMETHYLENE 2 OXO 1,2,3,4 TETRAHYDROQUINOXALINES AS START
  179805. VOL 23   1985  PG 2083a
  179806. GABRIEL WEATHERHEAD
  179807. 12630
  179808. JOCC-MARTIN REVIEW NMR COSY 2D PROTON SPECTROSCOPYM
  179809. 13639N
  179810. 2/28/96V5TWO DIMENSIONAL NMR STUDIES USING THE COSY TECHNIQUE.W
  179811. VOL 50   1985  PG 2383a
  179812. GABRIEL WEATHERHEAD
  179813. 12631
  179814. JACSCQVINYL CYCLOPROPANE CYCLOPENTENE CARBANION SULFONE REARRANGEMENT ALKYLATION REVIEWM
  179815. 13640N
  179816. 2/28/96V6CARBANION ACCELERATED VINYLCYCLOPROPANE REARRANGEMENT.W
  179817. VOL 107   1985  PG 4579a
  179818. GABRIEL WEATHERHEAD
  179819. 12632
  179820. COMPREHENSIVE ORG. CHEMISTRYC.DURST CARBANION SULFONE REVIEW ALKYLATION BASEM
  179821. 13641N
  179822. 2/28/96V=REVIEW OF THE CHEMISTRY OF SULFONYL CARBANION AND ALKYLATION.W
  179823. VOL 0   1979  PG 171a
  179824. GABRIEL WEATHERHEAD
  179825. 12633
  179826. TETRAHEDRONC/MAGNUS CARBANION SULFONE REVIEW ALKYLATION BASEM
  179827. 13642N
  179828. 2/28/96VEANOTHER REVIEW OF THE ALKYLATION OF CARBANIONS DERIVED FROM SULFONES.W
  179829. VOL 33   1977  PG 2019a
  179830. GABRIEL WEATHERHEAD
  179831. 12634
  179832. ACC CHEM RES
  179833. CBMENGER INTRAMOLECULAR REVIEW LACTONIZATION ENZYME PHYSICAL ORGANICM
  179834. 13643N
  179835. 2/28/96V2SOURCE OF INTRAMOLECULAR AND ENZYMATIC REACTIVITY.W
  179836. VOL 18   1985  PG 128a
  179837. GABRIEL WEATHERHEAD
  179838. 12635
  179839. ACC CHEM RESCNVIEHE CAPTODATIVE MEROSTABILIZATION RADICAL DIMERIZATION DONOR ACCEPTOR REVIEWM
  179840. 13644N
  179841. 2/28/96V
  179842. THE CAPTODATIVE EFFECTW
  179843. VOL 18   1985  PG 148a
  179844. GABRIEL WEATHERHEAD
  179845. 12636
  179846. JCS PERKIN 1CGDIAZO ALDEHYDE REDUCTION LITHIATE ESTER CARBANION CONDENSATION ADDITIONM
  179847. 13645N
  179848. 2/28/96VeREDUCTION OF DIAZO B HYDROXY ESTERS TO HYDROXY ESTERS. (INCLUDES REVIEW ON REDUCTION OF DIAZO GROUP).W
  179849. VOL 0   1985  PG 493a
  179850. GABRIEL WEATHERHEAD
  179851. 12637
  179852. TETCACARBOXYL ESTERIFICATION THIO ESTER AMIDE PROTECTION REVIEW KETONEM
  179853. 13646N
  179854. 2/28/96VLREVIEW OF METHODS FOR ESTERIFICATION AND PROTECTION OF THE CAR  BOXYL GROUP.W
  179855. VOL 36   1980  PG 2409a
  179856. GABRIEL WEATHERHEAD
  179857. 12638
  179858. CUBARTLETT SYNTHESIS NATURAL PRODUCT STEREOSELECTIVE ASYMMETRIC INDUCTION REVIEW CHIRALM
  179859. 13647N
  179860. 2/28/96VdSTEREOCHEMICAL CONTROL IN SYNTHESIS OF ACYCLIC SYSTEMS: APPLI  CATIONS TO NATURAL PRODUCT SYNTHESIS.W
  179861. VOL 36   1980  PG 3a
  179862. GABRIEL WEATHERHEAD
  179863. 12639
  179864. JOCCGALONSO METAL DIAZO TRANSITION WRITING CYCLOADDITION CYCLOPROPANE REVIEWM
  179865. 13648N
  179866. 2/28/96V7TRANSITION METAL ASSISTED REACTIONS OF DIAZO COMPOUNDS.W
  179867. VOL 50   1985  PG 988a
  179868. GABRIEL WEATHERHEAD
  179869. 12640
  179870. TET LETTC=BROWN ULTRASOUND REVIEW REFERENCE HYDROBORATION WRITING BORONM
  179871. 13649N
  179872. 2/28/96VNULTRASONICS IN ORGANOBORANE CHEMISTRY POWERFUL METHOD FOR RAPID HYDROBORATION.W
  179873. VOL 0   1985  PG 2187a
  179874. GABRIEL WEATHERHEAD
  179875. 12641
  179876. CHEM SOC REVCMREVIEW NICKEL ORGANOMETALLIC CYCLIZATION ALLYLIC RING CLOSURE METAL SYNTHESISM
  179877. 13650N
  179878. 2/28/96VDPI ALLYLNICKEL HALIDES AS SELECTIVE REAGENTS IN ORGANIC SYN  THESIS.W
  179879. VOL 14   1985  PG 94a
  179880. GABRIEL WEATHERHEAD
  179881. 12642
  179882. CHEM REV
  179883. CQJOHNSTONE REVIEW HYDROGENATION REDUCTION CATALYST EXPERIMENTAL PALLADIUM HYDROGENM
  179884. 13651N
  179885. 2/28/96VQHETEROGENOUS CATALYTIC TRANSFER HYDROGENATION FOR REDUCTION OF ORGANIC COMPOUNDS.W
  179886. VOL 85   1985  PG 129a
  179887. GABRIEL WEATHERHEAD
  179888. 12643
  179889. B    SYNTHESISCLPARNES SYNTHESIS SILICON DESILYLATION EQUIVALENT LEWIS ACID CARBANION REVIEWM
  179890. 13652N
  179891. 2/28/96V.REVIEW OF LEWIS ACID DESILYLATION IN SYNTHESISW
  179892. VOL 0   1984  PG 992a
  179893. GABRIEL WEATHERHEAD
  179894. 12644
  179895. TETCAREVIEW PREPARATION THIOPHOSGENE THIOAMIDE HALIDE THIO AMIDE SILYLM
  179896. 13653N
  179897. 2/28/96V'PREPARATION OF THIOCARBAMOYL CHLORIDES.W
  179898. VOL 36   1980  PG 539a
  179899. GABRIEL WEATHERHEAD
  179900. 12645
  179901. TETCHISOMERIZATION REVIEW OLEFIN EPOXIDE THIIRANE AZIRIDINE ALKENE EPISULFIDEM
  179902. 13654N
  179903. 2/28/96V
  179904. REVIEW: OLEFIN INVERSION.W
  179905. VOL 36   1980  PG 557a
  179906. GABRIEL WEATHERHEAD
  179907. 12646
  179908. JACSCBCLAISEN COPE TRANSITION METAL CATALYST INTRODUCTION WRITING REVIEWM
  179909. 13655N
  179910. 2/28/96
  179911. V7TRANSITION METAL CATALYZED CLASEN REARRANGEMENTS. _____W
  179912. VOL 107   1985  PG 2058a
  179913. GABRIEL WEATHERHEAD
  179914. 12647
  179915. TETC<KATRITZKY AMINE PYRYLIUM CATION PYRIDINIUM REVIEW CONVERSIONM
  179916. 13656N
  179917. 2/28/96VYREVIEW: CONVERSION OF PRIMARY AMINO GROUPS INTO OTHER FUNCTION  ALITY BY YRYLIUM CATIONS.W
  179918. VOL 36   1980  PG 679a
  179919. GABRIEL WEATHERHEAD
  179920. 12648
  179921. TETC2FODOR ISOQUINOLINE NITRILIUM SALT MECHANISM REVIEWM
  179922. 13657N
  179923. 2/28/96VdBISCHLER NAPIERALSKI AND RELATED REACTIONS REVIEW AND MECHA  NISMS VIA NITRILIUM SALT INTERMEDIATES.W
  179924. VOL 36   1980  PG 1279a
  179925. GABRIEL WEATHERHEAD
  179926. 12649
  179927. TETRAHEDRONCCPLATZ CARBENE THEORY REVIEW WRITING SPECTROSCOPY CYCLOPROPENE DIAZOM
  179928. 13658N
  179929. 2/28/96V/RECENT ASPECTS OF CARBENE CHEMISTRY. A REVIEW .W
  179930. VOL 0   YR[0]   PG 1423a
  179931. GABRIEL WEATHERHEAD
  179932. 12650
  179933. ACTA CHEM SCANDA BCPTORSSELL DIPOLAR CYCLOADDITION ISOXAZOLIDINE NITRILE NITRONE OXIME REVIEW ALKENEM
  179934. 13659N
  179935. 2/28/96V*1,3 DIPOLAR ADDITION OF OXIMES TO OLEFINS.
  179936. VOL 38   1984  PG 423a
  179937. GABRIEL WEATHERHEAD
  179938. 12651
  179939. B    SYNTHESISCBREVIEW CONJUGATE ADDITION CUPRATE ENONE TRAP TRAPPING ELECTROPHILEM
  179940. 13660N
  179941. 2/28/96V;ORGANOCOPPER CONJUGATE ADDITION ENOLATE TRAPPING REACTIONS.W
  179942. VOL 0   1985  PG 364a
  179943. GABRIEL WEATHERHEAD
  179944. 12652
  179945. B    J CHEM EDC)MACOMBER NMR FT REVIEW SPECTROSCOPY TEACHM
  179946. 13661N
  179947. 2/28/96V/A PRIMER ON FOURIER TRANSFORM  NMR SPECTROSCOPYW
  179948. VOL 62   1985  PG 213a
  179949. GABRIEL WEATHERHEAD
  179950. 12653
  179951. CHEM SOC REVC@BILLINGTON NICKEL REVIEW PI ALLYL METAL ORGANOMETALLIC SYNTHESISM
  179952. 13662N
  179953. 2/28/96VCPI ALLYL NICKEL HALIDES AS SELECTIVE REAGENTS IN ORGANIC SYNTHESIS.W
  179954. VOL 0   1985  PG 93a
  179955. GABRIEL WEATHERHEAD
  179956. 12654
  179957. JOCCHTALLEY QUINONE ORTHO METHIDE INTRAMOLECULAR DIELS ALDER REVIEW REFERENCEM
  179958. 13663N
  179959. 2/28/96VLSTEREOSPECIFIC INTRAMOLECULAR DIELS ALDER REACTION OF AN O QUI  NONE METHIDEW
  179960. VOL 50   1985  PG 1695a
  179961. GABRIEL WEATHERHEAD
  179962. 12655
  179963. C7FLUORIDE ION NAKED BASE CROWN ETHER DESILYLATION REVIEWM
  179964. 13664N
  179965. 2/28/96VQNAKED FLUORIDE CHEMISTRY A REVIEW OF AVAILABLE REAGENTS FROM FLUKA ON COVER SHEETW
  179966. VOL 50   1985  PG 1350a
  179967. GABRIEL WEATHERHEAD
  179968. 12656
  179969. BULL SOC CHIM BELGCEHUISGEN THIOCARBONYL YLIDE REVIEW DIPOLAR CYCLOADDITION SULFUR DIPOLEM
  179970. 13665N
  179971. 2/28/96V<RECENT DEVELOPMENTS OF THE CHEMISTRY OF THIOCARBONYL YLIDES.W
  179972. VOL 93   1984  PG 511a
  179973. GABRIEL WEATHERHEAD
  179974. 12657
  179975. JACSC@CRAM CHIRAL INDUCTION ADDITION ASYMMETRIC CARBONYL FELKIN REVIEWM
  179976. 13666N
  179977. 2/28/96V4ASYMMETRIC ELECTROPHILIC ADDITION WITH 1,2 INDUCTIONW
  179978. VOL 107   1985  PG 3603a
  179979. GABRIEL WEATHERHEAD
  179980. 12658
  179981. B    SYNTHESISCORIPOLL CYCLOREVERSION SYNTHESIS HETEROCYCLE CARBOCYCLE RETRO DIELS ALDER REVIEWM
  179982. 13667N
  179983. 2/28/96VJEXTENSIVE REVIEW WITH NUMEROUS HETEROCYCLIC EXAMPLES CONC SINCE 1980 OR SOW
  179984. VOL 0   1985  PG 122a
  179985. GABRIEL WEATHERHEAD
  179986. 12659
  179987. ANGEW CHEM INT ED ENGL
  179988. CLMASAMUNE REVIEW ASYMMETRIC SYNTHESIS STEREOCHEM CHIRAL INDUCTION DIELS ALDERM
  179989. 13668N
  179990. 2/28/96VaDOUBLE ASYMMETRIC SYNTHESIS AND A NEW STRATEGY FOR STEREO  CHEMICAL CONTROL IN ORGANIC SYNTHESIS.W
  179991. VOL 24   1985  PG 1a
  179992. GABRIEL WEATHERHEAD
  179993. 12660
  179994. B    SYNTHESISC3REVIEW AMINE STERIC HINDRANCE BASE NITROGEN HARPOONM
  179995. 13669N
  179996. 2/28/96V'REVIEW ON HINDERED AMINES (PIPERIDINES)W
  179997. VOL 0   1984  PG 896a
  179998. GABRIEL WEATHERHEAD
  179999. 12661
  180000. B    SYNTHESISC4YOKUYAMA REVIEW SULFUR CARBON DISULFIDE CS2 ADDITIONM
  180001. 13670N
  180002. 2/28/96V&REACTIONS OF CARBON DISULFIDE (REVIEW)W
  180003. VOL 84   1984  PG 798a
  180004. GABRIEL WEATHERHEAD
  180005. 12662
  180006. J ORGANOMETALLIC CHEMC@HEGEDUS REVIEW ORGANOMETALLIC METAL TRANSITION SYNTHESIS ORGANICM
  180007. 13671N
  180008. 2/28/96V6USE OF TRANSITION METALS IN ORGANIC SYNTHESIS A REVIEWW
  180009. VOL 283   1985  PG 1a
  180010. GABRIEL WEATHERHEAD
  180011. 12663
  180012. RECUEIL TRAV CHIMC7WIERSUM FLASH REVIEW PYROLYSIS VACUUM SYNTHESIS WRITINGM
  180013. 13672N
  180014. 2/28/96
  180015. V`FLASH VACUUM PYROLYSIS   A VERSATILE METHOD IN ORGANIC CHEMISTRY SEE NEXT ISSUE FOR CONTINUATIONW
  180016. VOL 82   1982  PG 317a
  180017. GABRIEL WEATHERHEAD
  180018. 12664
  180019. RECUEIL TRAV CHIMCEZWANENBURG SULFUR SULFENE REVIEW PREPARATION CYCLOADDITION STEREOCHEMM
  180020. 13673N
  180021. 2/28/96V/A REVIEW DEALING WITH THE CHEMISTRY OF SULFINESW
  180022. VOL 101   1982  PG 1a
  180023. GABRIEL WEATHERHEAD
  180024. 12665
  180025. RECUEIL CHIM TRAVC:PETERS NMR LANTHANIDE SHIFT REVIEW STRUCTURE DETERMINATIONM
  180026. 13674N
  180027. 2/28/96VmMULTINUCLEAR NMR USING LANTHANIDE SHIFT REAGENTS AS AN ANALYTICAL TOOL FOR STRUCTURE DETERMINATION INSOLUTIONW
  180028. VOL 102   1983  PG 381a
  180029. GABRIEL WEATHERHEAD
  180030. 12666
  180031. TETRAHEDRONCCHEGEDUS PALLADIUM CYCLIZATION AMINE ALKENE HETEROCYCLE REVIEW METALM
  180032. 13675N
  180033. 2/28/96VUPALLADIUM ASSISTED REACTIONS OF MONO OLEFINS TO CYCLIZE INTO HETEROAROMATIC COMPOUNDSW
  180034. VOL 13   1984  PG 2416a
  180035. GABRIEL WEATHERHEAD
  180036. 12667
  180037. TETRAHEDRON
  180038. CKALKYNE EQUIVALENT SULFONE SULFONYL ACETYLENE CYCLOADDITION REVIEW REDUCTIONM
  180039. 13676N
  180040. 2/28/96V0ACETYLENE EQUIVALENTS IN CYCLOADDITION PROCESSESW
  180041. VOL 14   1984  PG 2585a
  180042. GABRIEL WEATHERHEAD
  180043. 12668
  180044. TETRAHEDRONCGHICKMOTT REVIEW ENAMINE CONJUGATE BUTADIENE BUTADIENYL DIENYL DIENAMINEM
  180045. 13677N
  180046. 2/28/96V7RECENT ADVANCES IN THE CHEMISTRY OF CONJUGATED ENAMINESW
  180047. VOL 40   1984  PG 2989a
  180048. GABRIEL WEATHERHEAD
  180049. 12669
  180050. TETRAHEDRONCCLIPSHUTZ CUPRATE REVIEW HIGHER ORDER NITRILE CYANO COPPER CONJUGATEM
  180051. 13678N
  180052. 2/28/96V,THE CHEMISTRY OF HIGHER ORDER ORGANOCUPRATESW
  180053. VOL 40   1984  PG 5005a
  180054. GABRIEL WEATHERHEAD
  180055. 12670
  180056. TETRAHEDRONCAREVIEW HARD SOFT ACID BASE CHEMOSELECTIVITY REGIOCHEM SELECTIVITYM
  180057. 13679N
  180058. 2/28/96VSCHEMOSELECTIVITY OF ORGANOMETALLIC REACTIONS USING PRINCIPLE OF HARD SOFT ACID BASEW
  180059. VOL 41   1984  PG 3a
  180060. GABRIEL WEATHERHEAD
  180061. 12671
  180062. B    SYNTHESISCLRAMAIH ANNELATION FIVE RING ENONE REVIEW CYCLOPENTENONE ALDOL INTRAMOLECULARM
  180063. 13680
  180064. 2/28/96V5CYCLOPENTA ANNELLATION REACTIONS IN ORGANIC SYNTHESISW
  180065. VOL 0   1984  PG 530a
  180066. GABRIEL WEATHERHEAD
  180067. 12672
  180068. B    SYNTHESISCQREVIEW EPOXIDE OXIRANE RING OPENING SYNTHESIS NUCLEOPHILIC EXPERIMENTAL REFERENCEM
  180069. 13681N
  180070. 2/28/96V*SYNTHETICALLY USEFUL REACTIONS OF EPOXIDESW
  180071. VOL 0   1984  PG 631a
  180072. GABRIEL WEATHERHEAD
  180073. 12673
  180074. B    SYNTHESISC?FLUKA SODIUM ACETYLIDE REAGENT ALKYNE ACETYLENE ADDITION REVIEWM
  180075. 13682N
  180076. 2/28/96VXUSE OF SODIUM ACETYLIDE IN ORGANIC SYNTHESIS   REVIEW ON COVER PAGE WITH MANY REFERENCESW
  180077. VOL 0   1984  PG 708a
  180078. GABRIEL WEATHERHEAD
  180079. 12674
  180080. B    SYNTHESISC>FLUKA NAKED FLUORIDE REVIEW REAGENT SILICON DESILYLATION CROWNM
  180081. 13683N
  180082. 2/28/96VGUSE OF NAKED FLUORIDE REAGENTS FOR DESILYLATION   REVIEW ON FRONT COVERW
  180083. VOL 0   1984  PG 796a
  180084. GABRIEL WEATHERHEAD
  180085. 12675
  180086. B    SYNTHESISC6YOKOYAMA CARBON DISULFIDE REVIEW CS2 REAGENT REFERENCEM
  180087. 13684N
  180088. 2/28/96V7ORGANIC REACTION OF CARBON DISULFIDE AND OVERALL REVIEWW
  180089. VOL 0   1984  PG 798
  180090. GABRIEL WEATHERHEAD
  180091. 12676
  180092. B    SYNTHESISC0DAGONNEAN HINDERED BASE AMINE PREPARATION REVIEWM
  180093. 13685N
  180094. 2/28/96V6PREPARATION AND USE OF HIGHLY HINDERED AMINES AS BASESW
  180095. VOL 0   1984  PG 895a
  180096. GABRIEL WEATHERHEAD
  180097. 12677
  180098. B    SYNTHESISC?PARNES SILICON LEWIS ACID ALLYL SILYL REVIEW DESILYLATION VINYLM
  180099. 13686N
  180100. 2/28/96VKCLEAVAGE OF SILICON CARBON BONDS AND THEIR APPLICATION TO ORGANIC SYNTHESISW
  180101. VOL 0   1984  PG 991a
  180102. GABRIEL WEATHERHEAD
  180103. 12678
  180104. B    SYNTHESISC:AGER PETERSON ALKENE SYNTHESIS SILICON ALCOHOL BASE OLEFINM
  180105. 13687N
  180106. 2/28/96V!A REVIEW OF THE PETERSON REACTIONW
  180107. VOL 0   1984  PG 370a
  180108. GABRIEL WEATHERHEAD
  180109. 12679
  180110. B    SYNTHESISC>TSUJI ALKENE TERMINAL OXIDATION METHYL KETONE REVIEW PALLADIUMM
  180111. 13688N
  180112. 2/28/96VlPALLADIUM CATALYZERD OXIDATION OF TERMINAL ALKENES TO METHYL KETONES. BEST PROTECTING GROUP FOR METYL KETONEW
  180113. VOL 0   1984  PG 369a
  180114. GABRIEL WEATHERHEAD
  180115. 12680
  180116. ACTA CHEM SCAND
  180117. CHMALMBERG WRITING ELECTROCHEM REVIEW AMIDE STUDENT INTRODUCTION OXIDATIONM
  180118. 13689N
  180119. 2/28/96V>ELECTROCHEMICAL PREPARATION AND USE OF AMIDOALKYLATION REAGENTW
  180120. VOL 0   1984  PG 87a
  180121. GABRIEL WEATHERHEAD
  180122. 12681
  180123. CAN J CHEMCZFALLIS DIELS ALDER REVIEW INTRAMOLECULAR INTRODUCTION WRITING DIPOLAR CYCLOADDITION TARGETM
  180124. 13690N
  180125. 2/28/96VPSTUDIES OF INTRAMOLECULAR DIELS ALDER REACTIONS   A GOOD INTRODUCTION OF WRITINGW
  180126. VOL 62   1984  PG 1709a
  180127. GABRIEL WEATHERHEAD
  180128. 12682
  180129. CHEM REVC6LUTZ CATALYST CATALYSIS COPE CLAISEN ACID REVIEW METALM
  180130. 13691N
  180131. 2/28/96V0CATALYSIS OF THE COPE AND CLAISEN REARRANGEMENTSW
  180132. VOL 84   1984  PG 206a
  180133. GABRIEL WEATHERHEAD
  180134. 12683
  180135. CHEM REVC@STOWELL REVIEW CARBON THREE HOMOLOGATION REAGENT ENONE EXTENSIONM
  180136. 13692N
  180137. 2/28/96V THREE CARBEN HOMOLOGATING AGENTSW
  180138. VOL 84   1984  PG 409a
  180139. GABRIEL WEATHERHEAD
  180140. 12684
  180141. CHEM REVC=BEAK DIPOLE STABILIZED AMIDE CARBANION AMINE CHELATION REVIEWM
  180142. 13693N
  180143. 2/28/96
  180144. V)ALPHA METALLO AMINE SYNTHETIC EQUIVALENTSW
  180145. VOL 84   1984  PG 471a
  180146. GABRIEL WEATHERHEAD
  180147. 12685
  180148. HEREROCYCLESCHHETEROCYCLE IMIDAZOLE CARBANION ALKYLATION REVIEW METAL LITHIUM EXCHANGEM
  180149. 13694N
  180150. 2/28/96V>METALLATION AND METAL HALOGEN EXCHANGE REACTIONS OF IMIDAZOLESW
  180151. VOL 23   1985  PG 417a
  180152. GABRIEL WEATHERHEAD
  180153. 12686
  180154. HETEROCYCLESC8INDOLE SYNTHESIS NITRO AROMATIC REDUCTION ENAMINE REVIEWM
  180155. 13695N
  180156. 2/28/96V<THE LEIMGRUBER BATCHO INDOLE SYNTHESIS USING NITRO AROMATICSW
  180157. VOL 22   1985  PG 195a
  180158. GABRIEL WEATHERHEAD
  180159. 12687
  180160. HETEROCYCLESC\SPECKAMP AZOMETHINE YLIDE REVIEW ELECTROCYCLIZATION ELECTROCYCLIC VINYL CYCLIZATION ALKALOIDM
  180161. 13696N
  180162. 2/28/96VX1,5 ELECTROCYCLIZATION OF AZOMETHINE YLIDES AND THEIR APPLICATION FOR ALKALOID SYNTHESISW
  180163. VOL 21   1984  PG 213a
  180164. GABRIEL WEATHERHEAD
  180165. 12688
  180166. HETEROCYCLESC7SASAKI ALKYNE AMINE ADDITION HETEROCYCLE REVIEW WRITINGM
  180167. 13697N
  180168. 2/28/96
  180169. VAA ROUTE TO FUSED HETEROCYCLES INVOLVING AMINE ADDITION TO ALKYNESW
  180170. VOL 22   1984  PG 1225a
  180171. GABRIEL WEATHERHEAD
  180172. 12689
  180173. HETEROCYCLESCdLABLACH COMBIER AZOMETHINE YLIDE REVIEW HETEROAROMATIC DIPOLAR CYCLOADDITION IMINIUM CYCLIC AROMATICM
  180174. 13698N
  180175. 2/28/96V"REACTIVITY OF CYCLOIMMONIUM YLIDESW
  180176. VOL 22   1984  PG 2079a
  180177. GABRIEL WEATHERHEAD
  180178. 12690
  180179. J HET CHEMCAL'ABBE HETEROCYCLE REARRANGEMENT DIMROTH REVIEW THERMAL FIVE RINGM
  180180. 13699N
  180181. 2/28/96V?MOLECULAR REARRANGEMENTS OF FIVE MEMBRANE RING HETEROMONOCYCLESW
  180182. VOL 21   1984  PG 627a
  180183. GABRIEL WEATHERHEAD
  180184. 12691
  180185. J HET CHEMC)CASTLE NMR 2D SPECTROSCOPY REVIEW WRITINGM
  180186. 13700N
  180187. 2/28/96V;TWO DIMENSIONAL NMR TO OBTAIN VICINAL PROTON CONNECTIVITIESW
  180188. VOL 21   1984  PG 929a
  180189. GABRIEL WEATHERHEAD
  180190. 12692
  180191.     B    SYNTHESISCLRIPOLL RETRO CYCLOADDITION CYCLOREVERSION REVIEW DIELS ALDER FLASH SYNTHESISM
  180192. 13701N
  180193. 2/28/96VQNEW SYNTHETIC DEVELOPMENTS OF THE 4+2 CYCLOREVERSION REACTION A REVIEW SINCE 1976
  180194. VOL 0   1985  PG 121a
  180195. GABRIEL WEATHERHEAD
  180196. 12693
  180197. B    SYNTHESISC>UCHIDA REVIEW HIGH PRESSURE CYCLOADDITION WRITING INTRODUCTIONM
  180198. 13702N
  180199. 2/28/96V%ORGANIC SYNTHESIS UNDER HIGH PRESSUREW
  180200. VOL 0   1985  PG 0a
  180201. GABRIEL WEATHERHEAD
  180202. 12694
  180203. JACSC?TROST STEREOCHEM CARBANION SULFONE ASYMMETRIC ALKYLATION REVIEWM
  180204. 13703N
  180205. 2/28/96V5STEREOCHEMISTRY OF ALLYL SULFONE CARBANION ALKYLATIONW
  180206. VOL 107   1985  PG 391a
  180207. GABRIEL WEATHERHEAD
  180208. 12695
  180209. CHEM REVCMHURD PREPARATION HYDROLYSIS CONDENSATION THIOAMIDE OXIDATION REDUCTION REVIEWM
  180210. 13704N
  180211. 2/28/96V5THE PREPARATION AND CHEMICAL PROPERTIES OF THIOAMIDESW
  180212. VOL 61   YR[61]   PG 45a
  180213. GABRIEL WEATHERHEAD
  180214. 12696
  180215. JCS QUARTERLY REVIEWC<TRIPPETT REVIEW METHODOLOGY PHOSPHERANE WITTIG BETAINE YLIDEM
  180216. 13705N
  180217. 2/28/96V
  180218. THE WITTIG REACTION: A REVIEWW
  180219. VOL 0   YR[0]   PG 406a
  180220. GABRIEL WEATHERHEAD
  180221. 12697
  180222. B    SYNTHESISC*REVIEW METHODOLOGY CATALYST PHASE TRANSFERM
  180223. 13706N
  180224. 2/28/96
  180225. V"REVIEW OF PHASE TRANSFER CATALYSTSW
  180226. VOL 0   1973  PG 441a
  180227. GABRIEL WEATHERHEAD
  180228. 12698
  180229. TET LETTCBKITA ANHYDRIDE SYNTHESIS SILICON PREPARATION REAGENT DIACID REVIEWM
  180230. 13707N
  180231. 2/28/96V4A MILD AND FACILE SYNTHESIS OF CARBOXYLIC ANHYDRIDESW
  180232. VOL 0   1984  PG 6027a
  180233. GABRIEL WEATHERHEAD
  180234. 12699
  180235. J MED CHEMC?CONJUGATE ENONE PREPARATION SUCCINIMIDE REVIEW IMIDE ALKYLATIONM
  180236. 13708N
  180237. 2/28/96V)PREPARATION OF N SUBSTITUTED SUCCINIMIDESW
  180238. VOL 28   1985  PG 9a
  180239. GABRIEL WEATHERHEAD
  180240. 12700
  180241. CHEM INDC,VIEHE IMINIUM REVIEW CYCLIZATION HETEROCYCLEM
  180242. 13709N
  180243. 2/28/96VFFORMATION OF HETEROCYCLES FROM IMINIUM SALTS: BY CYCLIZATION REACTIONSW
  180244. VOL 0   1977  PG 386a
  180245. GABRIEL WEATHERHEAD
  180246. 12701
  180247. ALDRICHIMICA ACTAC/SZABO REVIEW ISOCYANATE REAGENT CHLORO SULFONYLM
  180248. 13710N
  180249. 2/28/96V0CHLOROSULFONYL ISOCYANATE AS A SYNTHETIC REAGENTW
  180250. VOL 10   1977  PG 23a
  180251. GABRIEL WEATHERHEAD
  180252. 12702
  180253. ANGE. CHEMIE
  180254. CGNOYORI PROSTAGLANDIN ENOLATE ENONE ACETAL EPOXIDE ORGANOMETALLIC REVIEWM
  180255. 13711N
  180256. 2/28/96V3PROSTAGLANDIN SYNTHESIS BY THREE COMPONENT COUPLINGW
  180257. VOL 23   1984  PG 847a
  180258. GABRIEL WEATHERHEAD
  180259. 12703
  180260. ALDRICH CHIM ACTAC7DOLPHIN CHEMISTRY ORGANIC STUDENT WOODWARD NOBEL REVIEWM
  180261. 13712N
  180262. 2/28/96V&AN ARTICLE ABOUT ROBERT BURNS WOODWARDW
  180263. VOL 10   1977  PG 3a
  180264. GABRIEL WEATHERHEAD
  180265. 12704
  180266. ALDRICH CHIM ACTAC=HASE ACYL REVIEW FORMYL SYNTHON CARBANION UMPOLUNG ALKYLATIONM
  180267. 13713N
  180268. 2/28/96V=A COMPILATION OF REFERENCES ON FORMYL AND ACYL ANION SYNTHONSW
  180269. VOL 14   1984  PG 73a
  180270. GABRIEL WEATHERHEAD
  180271. 12705
  180272. ALDRICH CHIM ACTAC3PHASE TRANSFER CATALYST REAGENT REVIEW EXPERIMENTALM
  180273. 13714N
  180274. 2/28/96V!PHASE TRANSFER CATALYSTS   A LISTW
  180275. VOL 9   1976  PG 45a
  180276. GABRIEL WEATHERHEAD
  180277. 12706
  180278. ALDRICH CHIM ACTACCWALLACE REVIEW HYDROXYL AMINE SULFONIC ACID REAGENT AMINE AMINATIONM
  180279. 13715N
  180280. 2/28/96V=HYDROXYLAMINE O SULFONIC ACID. A VERSATILE SYNTHETIC REAGENT.
  180281. VOL 13   1980  PG 3a
  180282. GABRIEL WEATHERHEAD
  180283. 12707
  180284. ALDRICH CHIM ACTACCLONG REVIEW SILVER OXIDATION REARRANGEMENT CYCLOADDITION ALKYLATIONM
  180285. 13716N
  180286. 2/28/96V-THE ROLE OF SILVER SALTS IN ORGANIC PROCESSESW
  180287. VOL 14   1984  PG 0a
  180288. GABRIEL WEATHERHEAD
  180289. 12708
  180290. ALDRICH CHIM ACTACHCROWN SYNTHESIS SELECTIVITY COMPLEX PHASE TRANSFER CATALYST REVIEW ETHERM
  180291. 13717N
  180292. 2/28/96V+CROWN ETHERS: MACROCYCLIC COMPLEXING AGENTSW
  180293. VOL 11   1978  PG 35a
  180294. GABRIEL WEATHERHEAD
  180295. 12709
  180296. ALDRICH CHIM ACTACMCLEAVAGE ESTER ETHER CONVERSION SILICON REVIEW REAGENT TRIMETHYL SILYL IODIDEM
  180297. 13718N
  180298. 2/28/96V
  180299. IODOTRIMETHYLSILANEW
  180300. VOL 11   1978  PG 39a
  180301. GABRIEL WEATHERHEAD
  180302. 12710
  180303. ALDRICH CHIM ACTAC=BRISTOW TIN REAGENT SYNTHESIS ORGANOMETALLIC REVIEW CARBANIONM
  180304. 13719N
  180305. 2/28/96V"TIN REAGENTS FOR ORGANIC SYNTHESISW
  180306. VOL 17   1984  PG 75a
  180307. GABRIEL WEATHERHEAD
  180308. 12711
  180309. ALDRICH CHIM ACTA
  180310. CISIEVERS NMR SPECTROSCOPY REAGENT PHYSICAL ORGANIC SHIFT LANTHANIDE REVIEWM
  180311. 13720N
  180312. 2/28/96V-PRACTICAL REVIEW OF LANTHANIDE SHIFT REAGENTSW
  180313. VOL 10   1977  PG 54a
  180314. GABRIEL WEATHERHEAD
  180315. 12712
  180316. ALDRICH CHIM ACTACKBESCHKE HETEROCYCLE PYRIDINE ALKYLATION NITROGEN OXIDATION REDUCTION REVIEWM
  180317. 13721N
  180318. 2/28/96V!REACTIONS OF CYCLOALKENOPYRIDINESW
  180319. VOL 10   1978  PG 13a
  180320. GABRIEL WEATHERHEAD
  180321. 12713
  180322. ALDRICH CHIM ACTACJNEWAZ SYNTHESIS LACTONE CYCLIZATION METHYLENE METHODOLOGY BUTENOLIDE ALPHAM
  180323. 13722N
  180324. 2/28/96V*REVIEW ON SYNTHESIS OF CONJUGATED LACTONESW
  180325. VOL 10   1977  PG 64a
  180326. GABRIEL WEATHERHEAD
  180327. 12714
  180328. ALDRICH CHIM ACTACFCROWN PHASE TRANSFER ALKYLATION ELIMINATION REDUCTION CHELATION REVIEWM
  180329. 13723N
  180330. 2/28/96V
  180331. REACTIONS WITH CROWN ETHERSW
  180332. VOL 10   1978  PG 17a
  180333. GABRIEL WEATHERHEAD
  180334. 12715
  180335. TETRAHEDRONCKHICKMOTT ENAMINE CONJUGATION NITROGEN SYNTHESIS ALKYLATION REVIEW CONJUGATEM
  180336. 13724N
  180337. 2/28/96V*REVIEW ON CHEMISTRY OF CONJUGATED ENAMINES
  180338. VOL 0   1985  PG 2989a
  180339. GABRIEL WEATHERHEAD
  180340. 12716
  180341. TETRAHEDRONC@PASTO ALLENE SYNTHESIS CYCLOADDITION ALKENE REVIEW PHOTOCHEM 2+2M
  180342. 13725N
  180343. 2/28/96V&RECENT DEVELOPMENT IN ALLENE CHEMISTRYW
  180344. VOL 0   1985  PG 2805a
  180345. GABRIEL WEATHERHEAD
  180346. 12717
  180347. ALDRICH CHIM ACTAC/BROWN BORON HYDROBORATION REVIEW REAGENT BORANEM
  180348. 13726N
  180349. 2/28/96V
  180350. SYNTHETIC USES OF BORANESW
  180351. VOL 7   1974  PG 43a
  180352. GABRIEL WEATHERHEAD
  180353. 12718
  180354. ALDRICH CHIM ACTAC?BROWN BORON REVIEW REDUCTION ETHER EPOXIDE KETONE HYDROBORATIONM
  180355. 13727N
  180356. 2/28/96V5TRIALKYLBOROHYDRIDES AS NEW VERSATILE REDUCING AGENTSW
  180357. VOL 7   1974  PG 55a
  180358. GABRIEL WEATHERHEAD
  180359. 12719
  180360. ALDRICH CHIM ACTAC>BROWN REVIEW BORON HYDROBORATION STEREOSELECTIVE ALKYNE ALKENEM
  180361. 13728N
  180362. 2/28/96V3SYNTHESIS AND APPLICATIONS OF VINYLIC ORGANOBORANESW
  180363. VOL 14   1981  PG 3a
  180364. GABRIEL WEATHERHEAD
  180365. 12720
  180366. ALDRICH CHIM ACTACUREVIEW CATALYST PHASE TRANSFER DICHLORO PREPARATION CARBENE DISPLACEMENT EXPERIMENTAL
  180367. 13729N
  180368. 2/28/96V=APPLICATIONS OF PHASE TRANSFER CATALYSIS IN ORGANIC SYNTHESISW
  180369. VOL 9   1976  PG 35a
  180370. GABRIEL WEATHERHEAD
  180371. 12721
  180372. ALDRICH CHIM ACTAC/PROTECTION ACID T BOC DEPROTECTION AMINE REVIEWM
  180373. 13730N
  180374. 2/28/96V#BOC ON   NEW AMINO PROTECTING GROUPW
  180375. VOL 9   1976  PG 47a
  180376. GABRIEL WEATHERHEAD
  180377. 12722
  180378. ALDRICH CHIM ACTAC(REVIEW HYDRAZINE AMINE OXIDATION DIIMIDEM
  180379. 13731N
  180380. 2/28/96V)HYDRAZINE   ROCKET FUEL TO SYNTHETIC TOOLW
  180381. VOL 13   1984  PG 33a
  180382. GABRIEL WEATHERHEAD
  180383. 12723
  180384. ALDRICH CHIM ACTACISCHMIDT IODOTRIMETHYLSILANE DESILYLATION REVIEW SILYL ETHER ESTER ALCOHOLM
  180385. 13732N
  180386. 2/28/96V4USES OF BROMOTRIMETHYLSILANE AND IODOTRIMETHYLSILANEW
  180387. VOL 2   1981  PG 31a
  180388. GABRIEL WEATHERHEAD
  180389. 12724
  180390. ALDRICH CHIM ACTACDSHARPLESS REVIEW EPOXIDATION ALCOHOL ALLYLIC EPOXIDE PEROXIDE CHIRALM
  180391. 13733N
  180392. 2/28/96VCUSE OF T BUTYL HYDROPEROXIDE OXYGENATIONS OF OLEFINS AND ACETYLENESW
  180393. VOL 4   1979  PG 63a
  180394. GABRIEL WEATHERHEAD
  180395. 12725
  180396. NATURAL PRODUCT REPORTSC?BENTLY ALKALOID REVIEW SYNTHESIS PHENYLETHYL AMINE ISOQUINOLINEM
  180397. 13734N
  180398. 2/28/96V0PHENYLETHYLAMINES AND THE ISOQUINOLINE ALKALOIDSW
  180399. VOL 0   1984  PG 355a
  180400. GABRIEL WEATHERHEAD
  180401. 12726
  180402. SMOLIN AND RAPOPORT (BOOK)CHSMOLIN AMINE PREPARATION IMINE REVIEW FORMALDEHYDE TRIAZINE RING OPENINGM
  180403. 13735N
  180404. 2/28/96VCPREPARATION OF 1,3,5 HEXAHYDROTRIAZINES S TRIAZINES AND DERIVATIVESW
  180405. VOL 0   YR[59]   PG 477a
  180406. GABRIEL WEATHERHEAD
  180407. 12727
  180408. ,B    SYNTHESISC8VARVOGLIS REVIEW IODINE SYNTHESIS HYPERVALENT IODINATIONM
  180409. 13736N
  180410. 2/28/96V0POLYVALENT IODINE COMPOUNDS IN ORGANIC SYNTHESISW
  180411. VOL 8   1984  PG 709a
  180412. GABRIEL WEATHERHEAD
  180413. 12728
  180414. TETRAHEDRONCQDELUCCHI ALKYNE CYCLOADDITION DIELS ALDER SYNTHESIS METHODOLOGY EQUIVALENT ALKENEM
  180415. 13737N
  180416. 2/28/96V:REVIEW OF ACETYLENE EQUIVALENTS IN CYCLOADDITION REACTIONSW
  180417. VOL 0   1984  PG 2586a
  180418. GABRIEL WEATHERHEAD
  180419. 12729
  180420. .B    SYNTHESIS
  180421. .CASMITH EPOXIDE REVIEW SYNTHESIS METHODOLOGY REDUCTION RING OPENINGM
  180422. 13738N
  180423. 2/28/96V*SYNTHETICALLY USEFUL REACTIONS OF EPOXIDESW
  180424. VOL 8   1984  PG 629a
  180425. GABRIEL WEATHERHEAD
  180426. 12730
  180427. JACSC>MARTIN NIH REVIEW ALKALOID WRITING TARGET ALDOL INTRAMOLECULARM
  180428. 13739N
  180429. 2/28/96V)SYNTHESIS OF THE AMARYLLIDACEAE ALKALOIDSW
  180430. VOL 106   1984  PG 6432a
  180431. GABRIEL WEATHERHEAD
  180432. 12731
  180433. JACSC:DANISHEFSHY NIH BIOLOGY REVIEW WRITING MITOMYCIN AZIRIDINEM
  180434. 13740N
  180435. 2/28/96V9REVIEW OF MITOMYCIN BEHAVIOR AND BIOLOGICAL JUSTIFICATIONW
  180436. VOL 106   1984  PG 6424a
  180437. GABRIEL WEATHERHEAD
  180438. 12732
  180439. 1B    SYNTHESISCETAYLOR REVIEW SYNTHESIS PROSTAGLANDIN STRATEGY TARGET NATURAL PRODUCTM
  180440. 13741N
  180441. 2/28/96VESTATEGIES EMPLOYED IN THE SYNTHESIS OF PROSTACYCLINS AND THROMBOXANESW
  180442. VOL 6   1984  PG 449a
  180443. GABRIEL WEATHERHEAD
  180444. 12733
  180445. 2B    SYNTHESISCJZAUGG ALKYLATION AMIDE SYNTHESIS REVIEW NUCLEOPHILIC SUBSTITUTION NITROGENM
  180446. 13742N
  180447. 2/28/96V#AMIDOALKYLATION REACTIONS AT CARBON
  180448. VOL 0   1984  PG 85a
  180449. GABRIEL WEATHERHEAD
  180450. 12734
  180451. BULL SOC CHIM BELGC]GRIGG AZOMETHINE YLIDE DIPOLAR CYCLOADDITION IMINE TAUTOMER PROTOTROPIC HYDROGEN SHIFT REVIEWM
  180452. 13743N
  180453. 2/28/96VTNEW PROTOTROPIC PROCESSES IN THE SYNTHESIS OF HETEROCYCLES VIA DIPOLAR CYCLOADDITIONW
  180454. VOL 0   1984  PG 593a
  180455. GABRIEL WEATHERHEAD
  180456. 12735
  180457. JOCC:KOHN INTRAMOLECULAR IMINIUM HART SPECKAMP CYCLIZATION ACYLM
  180458. 13744N
  180459. 2/28/96VEINTRAMOLECULAR INITIATED CYCLIZATION OF N ACYLIMINIUM SALTS. A REVIEWW
  180460. VOL 49   1984  PG 3812a
  180461. GABRIEL WEATHERHEAD
  180462. 12736
  180463. JOCC*REVIEW SILICON NAKED FLUORIDE REAGENT BASEM
  180464. 13745N
  180465. 2/28/96VKNAKED FLUORIDE CHEMISTRY AS A TECHNIQUE FOR DESILYLATION REACTIONS   REVIEWW
  180466. VOL 0   1984  PG 3676a
  180467. GABRIEL WEATHERHEAD
  180468. 12737
  180469. ORG REACTIONSCAWATT NITRILE CARBANION OXYGEN OXYGENATION ALKYLATION REVIEW CYANOM
  180470. 13746N
  180471. 2/28/96VDADDITION AND SUBSTITUTION REACTIONS OF NITRILE STABILIZED CARBANIONSW
  180472. VOL 0   1984  PG 32a
  180473. GABRIEL WEATHERHEAD
  180474. 12738
  180475. TETRAHEDRONCLHEGEDUS ALKENE METAL CATALYST PALLADIUM ORGANOMETALLIC SUBSTITUTION ADDITIONM
  180476. 13747N
  180477. 2/28/96V^A REVIEW COVERING P INDUCED NUCLEOPHILIC SUBSTITUTION OF ALKENES BY A VARIETY OF NUCLEOPHILES.W
  180478. VOL 0   1984  PG 2415a
  180479. GABRIEL WEATHERHEAD
  180480. 12739
  180481. 8B    SYNTHESISCLRAMAIAH REVIEW ANNELATION CYCLOPENTANE SYNTHESIS WITTIG NAZAROV CYCLOPROPANEM
  180482. 13748N
  180483. 2/28/96V4CYCLOPENTAUNNELLATION REACTIONS IN ORGANIC SYNTHESISW
  180484. VOL 7   1984  PG 529a
  180485. GABRIEL WEATHERHEAD
  180486. 12740
  180487. 9B    CHEM COMMCEACETYLIDE SODIUM ALKYLATION CARBANION REVIEW ALKYNE ADDITION CARBONYLM
  180488. 13749N
  180489. 2/28/96V,USE OF SODIUM ACETYLIDE IN ORGANIC SYNTHESISW
  180490. VOL 0   1984  PG 1196a
  180491. GABRIEL WEATHERHEAD
  180492. 12741
  180493. TET LETTC:KRAUS RADICAL REVIEW CYCLIZATION ALKENE LACTONE TIN IODIDEM
  180494. 13750N
  180495. 2/28/96V=THE TRANSFORMATIONS OF ALKENES INTO LACTONES USING IODOESTERSW
  180496. VOL 0   1984  PG 3939a
  180497. GABRIEL WEATHERHEAD
  180498. 12742
  180499. ALDRICH CHIM ACTA
  180500. ;CHWENTRUP FLASH REVIEW WRITING PYROLYSIS SIGMATROPIC REACTIVE INTERMEDIATEM
  180501. 13751N
  180502. 2/28/96V[PREPARATIVE FLASH VACUUM PYROLYSIS. A REVIEW OF FLASH VACUUM PYROLYSIS WITH MANY REFERENCESW
  180503. VOL 0   1984  PG 31a
  180504. GABRIEL WEATHERHEAD
  180505. 12743
  180506. <B    SYNTHESISCCSTANG TRIFLATE VINYL SYNTHESIS TRIFLIC ANHYDRIDE REVIEW PREPARATIONM
  180507. 13752N
  180508. 2/28/96V
  180509. SYNTHESIS OF VINYL TRIFLATESW
  180510. VOL 0   1980  PG 283a
  180511. GABRIEL WEATHERHEAD
  180512. 12744
  180513. =B    SYNTHESISCBSHANNON REVIEW SYNTHESIS TARGET SKELETON CARBAZOLE INDOLE ALKALOIDM
  180514. 13753N
  180515. 2/28/96V_SYNTHETIC APPROACHES TO ELLIPTICINES AND OTHER DERIVATIVES AND ANALOGUES OF 6H PYRIDO CARBAZOLEW
  180516. VOL 4   1984  PG 289a
  180517. GABRIEL WEATHERHEAD
  180518. 12745
  180519. >B    SYNTHESISC:BECKER REVIEW STILBENE PREPARATION ALKENE SYNTHESIS METHODM
  180520. 13754N
  180521. 2/28/96V
  180522. SYNTHESIS OF STILBENESW
  180523. VOL 5   1984  PG 341a
  180524. GABRIEL WEATHERHEAD
  180525. 12746
  180526. ?B#CURRENT TRENDS IN ORGANIC SYNTHESIS
  180527. ?CUSTORK REVIEW RADICAL CYCLIZATION INTRAMOLECULAR ADDITION STEREOELECTRONIC HETEROCYCLEM
  180528. 13755N
  180529. 2/28/96V3VINYL AND BETA ALKOXY RADICALS IN ORGANIC SYNTHESISW
  180530. VOL 0   1982  PG 5a
  180531. GABRIEL WEATHERHEAD
  180532. 12747
  180533. JOCCQJORGENSEN DIELS ALDER DIPOLAR SIGMATROPIC ELECTROCYCLIC PROGRAM PERICYCLIC REVIEWM
  180534. 13756N
  180535. 2/28/96V>GENERAL TREATMENT OF PERISELECTIVITY:  CAMEO  COMPUTER PROGRAMW
  180536. VOL 49   1984  PG 3001a
  180537. GABRIEL WEATHERHEAD
  180538. 12748
  180539. TETRAHEDRONC>BAIZER ELECTROCHEM SYNTHESIS METHODOLOGY CARBONYL REVIEW KOLBEM
  180540. 13757N
  180541. 2/28/96V.ELECTROCHEMISTRY IN ORGANIC SYNTHESIS (REVIEW)W
  180542. VOL 0   1984  PG 935a
  180543. GABRIEL WEATHERHEAD
  180544. 12749
  180545. JCS PERKIN IC;KATRITZKY YLIDE PYRIDINE REVIEW PYRIDINIUM SALT PREPARATIONM
  180546. 13758N
  180547. 2/28/96V
  180548. REACTION OF PYRIDINIUM YLIDESW
  180549. VOL 0   1984  PG 941a
  180550. GABRIEL WEATHERHEAD
  180551. 12750
  180552. TET LETTC3PIERS WRITING ANNULATION RING FUSION REVIEW STUDENTM
  180553. 13759N
  180554. 2/28/96
  180555. CVCA NEW ANNULATION SEQUENCE USING TRIMETHYLSTANNYL UNSATURATED ESTERSW
  180556. VOL 0   1984  PG 3155a
  180557. GABRIEL WEATHERHEAD
  180558. 12751
  180559. TET LETTCCLASZLO CONVERSION HYDROLYSIS KETONE HYDRAZONE CATALYST METAL REVIEWM
  180560. 13760N
  180561. 2/28/96VWCONVERSION OF DIMETHYLHYDRAZONES TO CARBONYL COMPOUNDS BY CLAY SUPPORTED FERRIC NITRATEW
  180562. VOL 0   1984  PG 3309a
  180563. GABRIEL WEATHERHEAD
  180564. 12752
  180565. ACCT CHEM RESCWOKI REVIEW CONFORMATION ROTATION ROTOMER PHYSICAL ORGANIC CONFORMATIONAL CURTIN HAMMETTM
  180566. 13761N
  180567. 2/28/96V$REACTIVITY OF CONFORMATIONAL ISOMERSW
  180568. VOL 17   1984  PG 154a
  180569. GABRIEL WEATHERHEAD
  180570. 12753
  180571. ACCT CHEM RESCCSKELL BROMINATION RADICAL BROMIDE MECHANISM PHYSICAL ORGANIC REVIEWM
  180572. 13762N
  180573. 2/28/96V'RADICAL BROMINATIONS OF ALLKYL BROMIDESW
  180574. VOL 17   1984  PG 160a
  180575. GABRIEL WEATHERHEAD
  180576. 12754
  180577. ANGEW CHEMCWCONIA REVIEW CYCLOBUTANE CYCLOPROPANE REARRANGEMENT CATALYST AZIRIDINE RING CONTRACTIONM
  180578. 13763N
  180579. 2/28/96
  180580. GVhRING CONTRACTIONS AND EXPANSIONS OF VICINALLY DISUBSTITUTED CYCLOBUTANES AND CYCLOPROPYLMETHYL COMPOUNDSW
  180581. VOL 14   1975  PG 473a
  180582. GABRIEL WEATHERHEAD
  180583. 12755
  180584. TETRAHEDRONC;SHONO OXIDATION AMINE ELECTROCHEM REVIEW ELECTROLYSIS KOLBEM
  180585. 13764N
  180586. 2/28/96V-ELECTROORGANIC CHEMISTRY IN ORGANIC SYNTHESISW
  180587. VOL 40   1984  PG 811a
  180588. GABRIEL WEATHERHEAD
  180589. 12756
  180590. TETRAHEDRONCQBAIZER ELECTROLYSIS SYNTHESIS ADDITION ELIMINATION CYCLIZATION ELECTROCHEM REVIEWM
  180591. 13765N
  180592. 2/28/96V8RECENT DEVELOPMENTS IN ORGANIC SYNTHESIS BY ELECTROLYSISW
  180593. VOL 40   1981  PG 935a
  180594. GABRIEL WEATHERHEAD
  180595. 12757
  180596. ANGEW CHEMC:MEIER REVIEW WOLFF REARRANGEMENT DIAZO KETONE KETENE METALM
  180597. 13766N
  180598. 2/28/96V3THE WOLFF REARRANGEMENT OF DIAZO CARBONYL COMPOUNDSW
  180599. VOL 14   1975  PG 32a
  180600. GABRIEL WEATHERHEAD
  180601. 12758
  180602. ANGEW CHEMCWADAM DIOXETANE CHEMILUMINESCENCE DECOMPOSITION FORMALDEHYDE PREPARATION PEROXIDE REVIEWM
  180603. 13767N
  180604. 2/28/96
  180605. KVK1,2 DIOXETANE: SYNTHESIS, CHARACTERIZATION, STABILITY AND CHEMILUMINESCENCEW
  180606. VOL 23   1984  PG 166a
  180607. GABRIEL WEATHERHEAD
  180608. 12759
  180609. ANGEW CHEMCEJENNER REVIEW PRESSURE DIELS ALDER COPE PERICYCLIC HIGH PRESSURE HIGHM
  180610. 13768N
  180611. 2/28/96VNHIGH PRESSURE KINETIC INVESTIGATIONS IN ORGANIC AND MACROMOLE  CULAR CHEMISTRYW
  180612. VOL 14   1975  PG 137a
  180613. GABRIEL WEATHERHEAD
  180614. 12760
  180615. ANGEW CHEMCIBREITMAIER REVIEW C13 SPECTROSCOPY PHYSICAL ORGANIC HINDERED ROTATION NMRM
  180616. 13769N
  180617. 2/28/96VS13C SPIN LATTICE RELAXATION TIMES AND THE MOBILITY OF ORGANIC MOLECULES IN SOLUTIONW
  180618. VOL 14   1975  PG 144a
  180619. GABRIEL WEATHERHEAD
  180620. 12761
  180621. REVIEW CHEM INTCISTEINMETZ REVIEW CYCLOPROPENE ALLENE VINYL CARBENE PHOTOCHEM CYCLOPROPANEM
  180622. 13770N
  180623. 2/28/96VBREACTIVE INTERMEDIATES IN THE INTERCONVERSION OF C3H4 HYDROCARBONSW
  180624. VOL 5   1984  PG 57a
  180625. GABRIEL WEATHERHEAD
  180626. 12762
  180627. BULL CHEM SOC JPNC7HIRAI LACTAM REVIEW CYCLOADDITION SYNTHESIS BIOLOGY NIHM
  180628. 13771N
  180629. 2/28/96
  180630. OV8REVIEW DEALING WITH SYNTHESIS OF BETA LACTAMS (SEE CARD)W
  180631. VOL 0   1984  PG 0a
  180632. GABRIEL WEATHERHEAD
  180633. 12763
  180634. PB    CHEM COMMCNVAN LEUSEN REVIEW TOSMIC HETEROCYCLE OXAZOLE REARRANGEMENT ISOCYANIDE SULFONYLM
  180635. 13772N
  180636. 2/28/96VDUSE OF TOSMIC IN ORGANIC SYNTHESIS. SEE CARD FOR LEADING REFERENCES.W
  180637. VOL 0   1984  PG 68a
  180638. GABRIEL WEATHERHEAD
  180639. 12764
  180640. JOCCFCOMINS ORTHO PROTECTION AMINE CARBANION ALKYLATION REVIEW BENZALDEHYDEM
  180641. 13773N
  180642. 2/28/96VQORTHO METALATION DIRECTED BY AMINO ALKOXIDES. SEE ARTICLE FOR LEADING REFERENCES.W
  180643. VOL 49   1984  PG 1078a
  180644. GABRIEL WEATHERHEAD
  180645. 12765
  180646. HETEROCYCLESC9CLARK REVIEW INDOLE SYNTHESIS NITRO REDUCTION ENAMINE DMFM
  180647. 13774N
  180648. 2/28/96V&THE LEIMGRUBER BATCHO INDOLE SYNTHESISW
  180649. VOL 22   1984  PG 195a
  180650. GABRIEL WEATHERHEAD
  180651. 12766
  180652. CAN J CHEMC7FALLIS REVIEW INTRAMOLECULAR DIELS ALDER TARGET WRITINGM
  180653. 13775N
  180654. 2/28/96VPINTRAMOLECULAR DIELS ALDER REACTIONS. RECENT ADVANCES AND SYNTHETIC APPLICATIONS
  180655. VOL 0   1984  PG 183a
  180656. GABRIEL WEATHERHEAD
  180657. 12767
  180658. ANGEW CHEM INT ED ENGLCJHOFFMANN ALLYL CATION EQUIVALENT REVIEW CYCLOADDITION DIENE CYCLOHEPTENONEM
  180659. 13776N
  180660. 2/28/96VTCYCLOADDITION OF ALLYL CATIONS TO 1,3 DIENES AS A METHOD TO PREPARE 7 MEMBERED RINGSW
  180661. VOL 0   1984  PG 2a
  180662. GABRIEL WEATHERHEAD
  180663. 12768
  180664. TETRAHEDRONCIWENDER REVIEW METHODOLOGY MACROCYCLE RING EXPANSION MEDIUM RING SYNTHESISM
  180665. 13777N
  180666. 2/28/96V5MACROEXPANSION METHODOLOGY: SYNTHESIS OF MEDIUM RINGSW
  180667. VOL 37   1981  PG 3967a
  180668. GABRIEL WEATHERHEAD
  180669. 12769
  180670. HETEROCYCLESC?FRIEDRICHSEN MESOIONIC REVIEW DIPOLAR CYCLOADDITION HETEROCYCLEM
  180671. 13778N
  180672. 2/28/96VFSIC MEMBERED MESOIONIC HETEROCYCLES OF THE QUINODIMETHANE DIANION TYPEW
  180673. VOL 19   1982  PG 1083a
  180674. GABRIEL WEATHERHEAD
  180675. 12770
  180676. PHOSPHOROUS AND SULFURC@THIO REVIEW ALKYLATION C13 ENAMIDE SPECTROSCOPY SULFUR THIOAMIDEM
  180677. 13779N
  180678. 2/28/96
  180679. WVuALKYLATION REACTIONS OF THIOAMIDES, ALKYLATION OF VINYLOGOUS THIOAMIDES + STEREOCHEMISTRY OF THE ALKYLATION PRODUCTS.W
  180680. VOL 17   YR[0]   PG 367a
  180681. GABRIEL WEATHERHEAD
  180682. 12771
  180683. XB    SYNTHESISCGNARASIMHAN AROMATIC ANION LITHIATION HETEROCYCLE REVIEW ORTHO CARBANIONM
  180684. 13780N
  180685. 2/28/96V3HETEROCYCLIC SYNTHESES BASED ON AROMATIC LITHIATIONW
  180686. VOL 0   1983  PG 958a
  180687. GABRIEL WEATHERHEAD
  180688. 12772
  180689. ANGEW CHEM INT ED ENGLCDTIDWELL CARBONIUM CATION REVIEW SOLVOLYSIS KINETICS UNSTABLE NITRILEM
  180690. 13781N
  180691. 2/28/96V
  180692. DESTABILIZED CARBOCATIONSW
  180693. VOL 23   1984  PG 20a
  180694. GABRIEL WEATHERHEAD
  180695. 12773
  180696. ANGEW CHEM INT ED ENGLCIHOFFMANN REVIEW ALLYL CATION BUTADIENE GENERATION CYCLOADDITION MECHANISMM
  180697. 13782N
  180698. 2/28/96VpTHE CYCLOADDITION OF ALLYL CATIONS TO 1,3 DIENES: GENERAL METHOD FOR THE SYNTHESIS OF SEVEN MEMBERED CARBOCYCLESW
  180699. VOL 23   1984  PG 1a
  180700. GABRIEL WEATHERHEAD
  180701. 12774
  180702. [B    SYNTHESISCHOXIDATION SELECTIVE REAGENT PREPARATION REVIEW MANGANESE DIOXIDE ALCOHOL
  180703. 13783N
  180704. 2/28/96V!OXIDATION USING MANGANESE DIOXIDEW
  180705. VOL 0   1976  PG 65a
  180706. GABRIEL WEATHERHEAD
  180707. 12775
  180708. TET LETTCBSCHLOSSER REVIEW BASE SUPER SCHLOSSER BUTYLLITHIUM BUTOXIDE ACTIVEM
  180709. 13784N
  180710. 2/28/96VFTHE SCHLOSSER BASE BUTYLLITHIUM AND TERT BUTOXIDE MIXTURES. (SEE CARD)W
  180711. VOL 0   1984  PG 741a
  180712. GABRIEL WEATHERHEAD
  180713. 12776
  180714. ]B    SYNTHESISCANITRILE SYNTHESIS AMINE ALKENE ALLYL REVIEW PREPARATION REDUCTIONM
  180715. 13785N
  180716. 2/28/96V#SYNTHESIS OF PRIMORY ALLYLIC AMINESW
  180717. VOL 0   1983  PG 685a
  180718. GABRIEL WEATHERHEAD
  180719. 12777
  180720. ^B    SYNTHESISCVSANTELLI NAZAROV CYCLIZATION REVIEW CYCLOPENTENONE ELECTROCYCLIC ACID ORBITAL SYMMETRYM
  180721. 13786N
  180722. 2/28/96V
  180723. NAZAROV CYCLIZATION. A REVIEWW
  180724. VOL 0   1983  PG 429a
  180725. GABRIEL WEATHERHEAD
  180726. 12778
  180727. _B    SYNTHESISCGNARASIMHAN AROMATIC ORTHO HETEROCYCLE CARBANION REVIEW ALKYLATION AMINEM
  180728. 13787N
  180729. 2/28/96VKSYNTHESIS OF HETEROCYCLIC COMPOUNDS INVOLVING AROMATIC LITHIATION REACTIONSW
  180730. VOL 0   1983  PG 957a
  180731. GABRIEL WEATHERHEAD
  180732. 12779
  180733. `B    SYNTHESISCFWHITESELL ENOLATE IMINE HYDRAZONE CARBANION ALKYLATION REVIEW NITROGENM
  180734. 13788N
  180735. 2/28/96VBALKYLATION OF KETONES AND ALDEHYDES VIA THEIR NITROGEN DERIVATIVESW
  180736. VOL 0   1984  PG 517a
  180737. GABRIEL WEATHERHEAD
  180738. 12780
  180739. TETRAHEDRONCAKIELBASINSKI CARBODIIMIDE IMIDE REVIEW ESTERIFICATION REAGENT DCCM
  180740. 13789N
  180741. 2/28/96V,RECENT DEVELOPMENT OF CARBODIIMIDE CHEMISTRYW
  180742. VOL 37   1981  PG 233a
  180743. GABRIEL WEATHERHEAD
  180744. 12781
  180745. CHIMIAC)SEEBACH REVIEW NITRO CONVERSION SYNTHESISM
  180746. 13790N
  180747. 2/28/96VCNITROALIPHATIC COMPOUNDS IDEAL INTERMEDIATES IN ORGANIC SYNTHESIS ?W
  180748. VOL 33   1979  PG 3a
  180749. GABRIEL WEATHERHEAD
  180750. 12782
  180751. JOCC;WARKENTIN CARBENE YLIDE HETEROATOM ADDITION TRAPPING REVIEWM
  180752. 13791N
  180753. 2/28/96V>CARBENE REACTION WITH HETEROATOMS TO GENERATE YLIDES. A REVIEWW
  180754. VOL 49   1984  PG 343a
  180755. GABRIEL WEATHERHEAD
  180756. 12783
  180757. CHEM REVCRSALAUN CYCLOPROPANE CYCLOPROPANONE HEMIACETAL ACETAL REVIEW SYNTHESIS RING OPENINGM
  180758. 13792N
  180759. 2/28/96
  180760. dVRCHEMISTRY OF CYCLOPROPANONE HEMIACETALS AND THEIR APPLICATION IN ORGANIC SYNTHESISW
  180761. VOL 83   1983  PG 619a
  180762. GABRIEL WEATHERHEAD
  180763. 12784
  180764. HETEROCYCLESCIBICYCLIC EXTRUSION HETEROATOM AROMATIC ARENE PREPARATION SYNTHESIS REVIEWM
  180765. 13793N
  180766. 2/28/96VYARENE SYNTHESES BY EXTRUSION OF HETEROATOMS FROM 7 HETEROBI  CYCLO[2.2.1]HEPTANE SYSTEMS.W
  180767. VOL 20   1983  PG 1816a
  180768. GABRIEL WEATHERHEAD
  180769. 12785
  180770. JACSCFSANCHEZ ALKALOID NIH WRITING STUDENT BIOLOGICAL REVIEW AMIDOALKYLATIONM
  180771. 13794N
  180772. 2/28/96V/TOTAL SYNTHESIS OF THE AMORYLLIDACEAE ALKALOIDSW
  180773. VOL 105   1983  PG 7640a
  180774. GABRIEL WEATHERHEAD
  180775. 12786
  180776. CHEM REVC?STANG CARBENE REVIEW ALKENE VINYL ADDITION TRIFLATE METHODOLOGYM
  180777. 13795N
  180778. 2/28/96V
  180779. UNSATURATED CARBENES. A REVIEWW
  180780. VOL 78   1978  PG 383a
  180781. GABRIEL WEATHERHEAD
  180782. 12787
  180783. JCS PERKIN ICBHOLMES CYCLOREVERSION DIPOLE DIPOLAR REVIEW WRITING METATHESIS NIHM
  180784. 13796N
  180785. 2/28/96VGFUNCTIONALIZATION OF ALKENES BY A CYCLOADDITION CYCLOREVERSION SEQUENCE
  180786. VOL 1   1983  PG 1243a
  180787. GABRIEL WEATHERHEAD
  180788. 12788
  180789. JCS PERKIN ICHPELTER INTRAMOLECULAR DIELS ALDER CYCLOADDITION FURAN HETEROCYCLE REVIEWM
  180790. 13797N
  180791. 2/28/96VFINTRAMOLECULAR DIELS ALDER REACTION OF FURANS AND RELATED HETEROCYCLESW
  180792. VOL 1   1983  PG 1383a
  180793. GABRIEL WEATHERHEAD
  180794. 12789
  180795. CHEM SOC REVC2GILCHRIST NITROSO ALKENE ALKYNE REVIEW DIELS ALDERM
  180796. 13798N
  180797. 2/28/96V#NITROSO ALKENES AND NITROSO ALKYNESW
  180798. VOL 12   1983  PG 53a
  180799. GABRIEL WEATHERHEAD
  180800. 12790
  180801. TETRAHEDRONCINEWKOME REVIEW CARBANION HETEROCYCLE AMINE ALKYLATION HETEROATOM NITROGENM
  180802. 13799N
  180803. 2/28/96V:HETEROATOM DIRECTED METALLATIONS IN HETEROCYCLIC SYNTHESISW
  180804. VOL 39   1983  PG 1955a
  180805. GABRIEL WEATHERHEAD
  180806. 12791
  180807. TETRAHEDRONC,BALDWIN LACTAM REVIEW PENICILLIN WRITING NIHM
  180808. 13800N
  180809. 2/28/96V/RECENT ASPECTS OF THE CHEMISTRY OF BETA LACTAMSW
  180810. VOL 39   1983  PG 2445a
  180811. GABRIEL WEATHERHEAD
  180812. 12792
  180813. TETRAHEDRON
  180814. mCIUTIMOTO REAGENT SILICON NITRILE CYANO CYANOTRIMETHYLSILANE REVIEW WRITINGM
  180815. 13801N
  180816. 2/28/96VQCYANOTRIMETHYLSILANE AS A VERSATILE REAGENT FOR INTRODUCING CYANIDE FUNCTIONALITYW
  180817. VOL 39   1983  PG 967a
  180818. GABRIEL WEATHERHEAD
  180819. 12793
  180820. TETRAHEDRONC5REICH REVIEW SILICON TARGET SYNTHESIS WRITING EPOXIDEM
  180821. 13802N
  180822. 2/28/96V>RECENT DEVELOPMENTS IN THE USE OF SILICON IN ORGANIC SYNTHESISW
  180823. VOL 39   1983  PG 841a
  180824. GABRIEL WEATHERHEAD
  180825. 12794
  180826. TETRAHEDRONC;MENGER DIRECTIONALITY ANGLE TRANSITION STATE BALDWIN REVIEWM
  180827. 13803N
  180828. 2/28/96V/DIRECTIONALITY OF ORGANIC REACTIONS IN SOLUTIONW
  180829. VOL 39   1983  PG 1013a
  180830. GABRIEL WEATHERHEAD
  180831. 12795
  180832. TETRAHEDRONC)KUEHNE INDOLE ALKALOID REVIEW NIH BIOLOGYM
  180833. 13804N
  180834. 2/28/96V#NEW DEVELOPMENT IN INDOLE ALKALOIDSW
  180835. VOL 39   1983  PG 3629a
  180836. GABRIEL WEATHERHEAD
  180837. 12796
  180838. TETRAHEDRONC@ALBRIGHT CARBANION ALKYLATION AMINE AMINO NITRILE REVIEW WRITINGM
  180839. 13805N
  180840. 2/28/96
  180841. qVOREACTIONS OF ACYL ANION EQUIVALENTS DERIVED FROM CYANOHYDRINS AND AMINONITRILESW
  180842. VOL 39   1983  PG 3207a
  180843. GABRIEL WEATHERHEAD
  180844. 12797
  180845. TETRAHEDRONCCRAO EPOXIDE OXIRANE PREPARATION EPOXIDATION CHIRAL REVIEW SHARPLESSM
  180846. 13806N
  180847. 2/28/96VIRECENT ADVANCES IN THE PREPARATION AND SYNTHETIC APPLICATIONS OF OXIRANESW
  180848. VOL 39   1983  PG 2323a
  180849. GABRIEL WEATHERHEAD
  180850. 12798
  180851. TETRAHEDRONCEBOGER TETRAZINE DIELS ALDER IMINE AZADIENE REVIEW HETEROCYCLE WRITINGM
  180852. 13807N
  180853. 2/28/96VPDIELS ALDER REACTIONS OF AZADIENES AND HETEROCYCLES CONTAINING A C N DOUBLE BONDW
  180854. VOL 39   1983  PG 2870a
  180855. GABRIEL WEATHERHEAD
  180856. 12799
  180857. HETEROCYCLESCCIDDON THIOPHENE CYCLOADDITION RING OPENING PHOTOCHEM CARBENE REVIEWM
  180858. 13808N
  180859. 2/28/96V=CYCLOADDITION, RING OPENING AND OTHER REACTIONS OF THIOPHENESW
  180860. VOL 20   1983  PG 1127a
  180861. GABRIEL WEATHERHEAD
  180862. 12800
  180863. TETRAHEDRONC6ASTRUC REVIEW IRON COMPLEX SYNTHESIS METHODOLOGY METALM
  180864. 13809N
  180865. 2/28/96
  180866. uVEORGANO IRON COMPLEXES OF AROMATIC COMPOUNDS. APPLICATION IN SYNTHESISW
  180867. VOL 39   1983  PG 4027a
  180868. GABRIEL WEATHERHEAD
  180869. 12801
  180870. TETRAHEDRONCKMARIANO REVIEW PHOTOCHEM IMINIUM AROMATIC SILICON ELECTRON TRANSFER WRITINGM
  180871. 13810N
  180872. 2/28/96VFTHE PHOTOCHEMISTRY OF IMINIUM SALTS AND RELATED HETEROAROMATIC SYSTEMSW
  180873. VOL 39   1983  PG 3845a
  180874. GABRIEL WEATHERHEAD
  180875. 12802
  180876. TETRAHEDRONC>REVIEW ACYL ANION EQUIVALENT CYANOHYDRIN NITRILE AMINE ALCOHOLM
  180877. 13811N
  180878. 2/28/96VmREACTIONS OF ACYL ANION EQUIVALENTS DERIVED FROM CYANOHYDRINS PROTECTED CYANOHYDRINS AND DIALKYLAMINONITRILESW
  180879. VOL 0   1983  PG 0a
  180880. GABRIEL WEATHERHEAD
  180881. 12803
  180882. ANGEW CHEM INT ED ENGLC<VIEHE REVIEW CAPTODATIVE MEROSTABILIZATION RADICAL STABILITYM
  180883. 13812N
  180884. 2/28/96V CAPTO DATIVE SUBSTITUTION EFFECTW
  180885. VOL 18   1979  PG 917a
  180886. GABRIEL WEATHERHEAD
  180887. 12804
  180888. TET LETTC<KISHI STEREOCHEM OSMIUM OXIDATION ALKENE DIOL REAGENT REVIEWM
  180889. 13813N
  180890. 2/28/96
  180891. yVESTEREOSELECTIVE GLYCOLIZATION OF ALLYLIC ALCOHOLS BY OSMIUM TETROXIDEW
  180892. VOL 0   1983  PG 3943a
  180893. GABRIEL WEATHERHEAD
  180894. 12805
  180895. HETEROCYCLESCDWONG ARENE EXTRUSION ALKYNE FURAN CYCLOADDITION AROMATIC DIELS ALDERM
  180896. 13814N
  180897. 2/28/96VfREVIEW OF ARENE SYNTHESIS BY EXTRUSION OF HETEROATOMS FROM 7 HETEROATOM BICYCLO[2.2.1]HEPTENE SYSTEMS.W
  180898. VOL 20   1983  PG 1815a
  180899. GABRIEL WEATHERHEAD
  180900. 12806
  180901. CHEM REVCGLEWARS OXIRENE PREPARATION REVIEW SMALL RING HETEROCYCLE PERACID ALKYNEM
  180902. 13815N
  180903. 2/28/96V$OXIRENES   PREPARATION AND CHEMISTRYW
  180904. VOL 83   1983  PG 519a
  180905. GABRIEL WEATHERHEAD
  180906. 12807
  180907. ANGEW CHEM INT ED ENGLCRADAM DIOXETANE SYNTHESIS PHOTOCHEM CHEMILUMINESCENCE REVIEW SINGLET OXYGEN BIOLOGYM
  180908. 13816N
  180909. 2/28/96VbFOUR MEMBERED RING PEROXIDES AS EXCITED STATE EQUIVALENTS: A NEW DIMENSION IN BIOORGANIC CHEMISTRYW
  180910. VOL 22   1983  PG 529a
  180911. GABRIEL WEATHERHEAD
  180912. 12808
  180913. ANGEW CHEM INT ED ENGL
  180914. }CGSTELLA INTRAMOLECULAR CYCLIZATION RADICAL CATION REVIEW PHOTOCHEM AMINEM
  180915. 13817N
  180916. 2/28/96V/HOMOLYTIC CYCLIZATIONS OF N CHLOROALKENYLAMINESW
  180917. VOL 22   1983  PG 339a
  180918. GABRIEL WEATHERHEAD
  180919. 12809
  180920. HETEROCYCLESCKTISLER AMIDINE HETEROCYCLE SYNTHESIS CYCLIZATION REVIEW PREPARATION REAGENTM
  180921. 13818N
  180922. 2/28/96VaREVIEW: HEREROCYCLIC AMIDINES AND HYDROXYAMIDINES AS SYNTHONS FOR BI  AND POLYCYCLIC HETEROCYCLESW
  180923. VOL 20   1983  PG 1591a
  180924. GABRIEL WEATHERHEAD
  180925. 12810
  180926. HETEROCYCLESCEDABOUN HETEROCYCLE NITROGEN SYNTHESIS REVIEW IMINE KETONE OXAZOLINONEM
  180927. 13819N
  180928. 2/28/96V@REVIEW: RECENT DEVELOPMENTS IN THE CHEMISTRY OF YLIDENE AZOLONESW
  180929. VOL 20   1983  PG 1615a
  180930. GABRIEL WEATHERHEAD
  180931. 12811
  180932. TETRAHEDRONCSHARTWIG REVIEW DEOXYGENATION ALCOHOL ALKANE RADICAL ION ELECTRON TRANSFER REDUCTIONM
  180933. 13820N
  180934. 2/28/96V8MODERN METHODS FOR THE RADICAL DEOXYGEMATION OF ALCOHOLSW
  180935. VOL 39   1983  PG 2609a
  180936. GABRIEL WEATHERHEAD
  180937. 12812
  180938. TETRAHEDRON
  180939. C:BOGER REVIEW DIELS ALDER AZADIENE NITROGEN AZA DIENE IMINEM
  180940. 13821N
  180941. 2/28/96V"DIELS ALDER REACTIONS OF AZADIENESW
  180942. VOL 39   1983  PG 2869a
  180943. GABRIEL WEATHERHEAD
  180944. 12813
  180945. TETRAHEDRONCCKLEIN REVIEW METALATION ALLYLIC BENZYL CARBANION ALKYLATION ENOLATEM
  180946. 13822N
  180947. 2/28/96V{DIRECT EFFECTS IN ALLYLIC AND BENZYLIC POLYMETALATIONS. THE QUESTION OF U STABILIZATION,Y AROMATICITY AND CROSS CONJUGATIONW
  180948. VOL 39   1983  PG 2733a
  180949. GABRIEL WEATHERHEAD
  180950. 12814
  180951. HETERO CHEMCDVAN LEUSEN REVIEW TOSMIC REAGENT NITRILE HETEROCYCLE PYRROLE OXAZOLEM
  180952. 13823N
  180953. 2/28/96VATOSMIC   USEFUL SYNTHETIC REAGENT IN ORGANIC CHEMISTRY (SEE CARD)W
  180954. VOL 5   1980  PG 5111a
  180955. GABRIEL WEATHERHEAD
  180956. 12815
  180957. B    SYNTHESISC$KUIVILA REDUCTION TIN HYDRIDE REVIEWM
  180958. 13824N
  180959. 2/28/96V4REDUCTION OF ORGANIC COMPOUNDS BY ORGANOTIN HYDRIDESW
  180960. VOL 0   1970  PG 499a
  180961. GABRIEL WEATHERHEAD
  180962. 12816
  180963. TET LETTC<HOOZ ENOL SILYL SILICON ETHER REVIEW PREPARATION METHODOLOGYM
  180964. 13825N
  180965. 2/28/96
  180966. VQRECENT REVIEW ON SYNTHESIS AND APPLICATIONS OF ENOL SILYL ETHERS  (SEE REF. NO.1)W
  180967. VOL 0   1983  PG 5695a
  180968. GABRIEL WEATHERHEAD
  180969. 12817
  180970. ANGEW CHEM INT ED ENGLC@BIANCHI RETRO DIPOLAR CYCLOADDITION REVIEW CYCLOREVERSION DIPOLEM
  180971. 13826N
  180972. 2/28/96V%REVIEW ON 1,3 DIPOLAR CYCLOREVERSION.W
  180973. VOL 18   1979  PG 721a
  180974. GABRIEL WEATHERHEAD
  180975. 12818
  180976. ANGEW CHEM INT ED ENGLC<HUENG REVIEW CYANIDE ACYL NITRILE PREPARATION CYANO CARBONYLM
  180977. 13827N
  180978. 2/28/96V
  180979. THE CHEMISTRY OF ACYL CYANIDESW
  180980. VOL 21   1982  PG 36a
  180981. GABRIEL WEATHERHEAD
  180982. 12819
  180983. TETRAHEDRONC[GINSBURG REVIEW DIPOLAR CYCLOADDITION ORBITAL SYMMETRY REGIOCHEM DIELS ALDER DIPOLAR THEORYM
  180984. 13828N
  180985. 2/28/96VKTHE ROLE OF SECONDARY ORBITAL INTERACTIONS IN CONTROLLING ORGANIC REACTIONSW
  180986. VOL 39   1983  PG 2095a
  180987. GABRIEL WEATHERHEAD
  180988. 12820
  180989. TETRAHEDRONCFROSNATI DIAZO MIGRATION CARBONIUM REARRANGEMENT REACTION REVIEW KETONEM
  180990. 13829N
  180991. 2/28/96
  180992. V{REACTIONS OF ALPHA DIAZOKETONES. ETHER OXYGEN PARTICIPATION IN THE ACETOLYSIS OF PHENOXY  AND DIPHENYLMETHOXY DIAZOKETONES.W
  180993. VOL 39   1983  PG 2259a
  180994. GABRIEL WEATHERHEAD
  180995. 12821
  180996. ACCT CHEM RESCOGASSMAN REVIEW CARBONIUM ELECTRON TRANSFER DEFICIENT WITH DRAWING NITRILE CYANOM
  180997. 13830N
  180998. 2/28/96V*ELECTRON DEFICIENT CARBOCATIONS. A REVIEW.W
  180999. VOL 16   1983  PG 279a
  181000. GABRIEL WEATHERHEAD
  181001. 12822
  181002. HETERO CHEMCJLEUSEN TOSMIC ISONITRILE CARBANION HETEROCYCLE REVIEW EXPERIMENTAL REAGENTM
  181003. 13831N
  181004. 2/28/96V0USE OF TOSMIC REAGENT FOR HETEROCYCLIC SYNTHESISW
  181005. VOL 5   1980  PG 111a
  181006. GABRIEL WEATHERHEAD
  181007. 12823
  181008. ANGEW CHEM INT ED ENGLCCCAUBERE REDUCTION CARBONYL REAGENT REVIEW HYDRIDE BORON METHODOLOGYM
  181009. 13832N
  181010. 2/28/96VQCOMPLEX REDUCING AGENTS   NOVEL WAYS OF USING SODIUM HYDRIDE IN ORGANIC SYNTHESISW
  181011. VOL 22   1983  PG 599a
  181012. GABRIEL WEATHERHEAD
  181013. 12824
  181014. HETEROCYCLESC.BROADBENT NMR ALKALOID SPECTROSCOPY C13 REVIEWM
  181015. 13833N
  181016. 2/28/96
  181017. V+CARBON 13 NMR IN ALKALOID CHEMISTRY. REVIEWW
  181018. VOL 20   1983  PG 863a
  181019. GABRIEL WEATHERHEAD
  181020. 12825
  181021. JACSC=TROST SULFUR THIO ENOL ETHER PREPARATION ALKYLATION CARBANIONM
  181022. 13834N
  181023. 2/28/96VTENOL THIOETHERS AS ENOL SUBSTITUTES AND THEIR USE IN ALKYLATION SEQUENCES. A REVIEW.W
  181024. VOL 105   1983  PG 5075a
  181025. GABRIEL WEATHERHEAD
  181026. 12826
  181027. CHEM REVCKSEEMAN REVIEW THEORY PHYSICAL ORGANIC CURTIN HAMMETT HAMMETT PRINCIPLE RATEM
  181028. 13835N
  181029. 2/28/96VPA REVIEW OF THE CURTIN HAMMETT PRINCIPLE AND ISTS ANALYSIS ON RATES OF REACTIONSW
  181030. VOL 83   1983  PG 84a
  181031. GABRIEL WEATHERHEAD
  181032. 12827
  181033. ANGEW CHEM INT ED ENGLCFSTELLA AMINE CHLORO RADICAL ADDITION REVIEW CYCLIZATION INTRAMOLECULARM
  181034. 13836N
  181035. 2/28/96V/HOMOLYTIC CYCLIZATIONS OF N CHLOROALKENYLAMINESW
  181036. VOL 0   1983  PG 338a
  181037. GABRIEL WEATHERHEAD
  181038. 12828
  181039. CHEM FUNCT GROUPS PATAI SERIESC:FATIADI REVIEW CYANO NITRILE PREPARATION SYNTHESIS REAGENTM
  181040. 13837N
  181041. 2/28/96
  181042. VUPREPARATION AND SYNTHETIC APPLICATIONS OF CYANO COMPOUNDS. A REVIEW OF THE LITERATUREW
  181043. VOL 0   1983  PG 30a
  181044. GABRIEL WEATHERHEAD
  181045. 12829
  181046. TETRAHEDRONC5MUKERJEE LACTAM AZETIDINONE REVIEW SYNTHESIS REACTIONM
  181047. 13838N
  181048. 2/28/96V/BETA LACTAMS: RETROSPECT AND PROSPECT. A REVIEWW
  181049. VOL 34   1978  PG 1731a
  181050. GABRIEL WEATHERHEAD
  181051. 12830
  181052. TETRAHEDRONCFZIMMERMAN DI PI METHANE PHOTOREARRANGEMENT SYNTHESIS STEREOCHEM REVIEWM
  181053. 13839N
  181054. 2/28/96VDTHE DI P METHANE REARRANGEMENT OF SYSTEMS WITH SIMPLE VINYL MOIETIESW
  181055. VOL 34   1978  PG 1775a
  181056. GABRIEL WEATHERHEAD
  181057. 12831
  181058. TETRAHEDRONCNNEWTON REVIEW MESOIONIC DIPOLE DIPOLAR DIPOLAR CYCLOADDITION SYDNONE MUNCHNONEM
  181059. 13840N
  181060. 2/28/96V
  181061. MESO IONIC HETEROCYCLESW
  181062. VOL 38   1982  PG 2966a
  181063. GABRIEL WEATHERHEAD
  181064. 12832
  181065. TETRAHEDRONC>HICKMOTT ENAMINE REVIEW SYNTHESIS CHEMISTRY REACTION MECHANISMM
  181066. 13841N
  181067. 2/28/96V]ENAMINES:RECENT ADVANCES IN SYNTHETIC, SPECTROSCOPIC, MECHANISTIC AND STEREO CHEMICAL ASPECTS
  181068. VOL 38   1982  PG 3363a
  181069. GABRIEL WEATHERHEAD
  181070. 12833
  181071. B    SYNTHESISC=BROWNBRIDGE REVIEW SYNTHESIS SILICON REAGENT SILYL ENOL ETHERM
  181072. 13842N
  181073. 2/28/96V&SILYL ENOL ETHERS IN SYNTHESIS PART IIW
  181074. VOL 2   1983  PG 85a
  181075. GABRIEL WEATHERHEAD
  181076. 12834
  181077. B    SYNTHESISC=BROWNBRIDGE SYNTHESIS REVIEW SILICON REAGENT SILYL ENOL ETHERM
  181078. 13843N
  181079. 2/28/96V
  181080. SILYL ENOL ETHERS IN SYNTHESISW
  181081. VOL 0   1983  PG 3a
  181082. GABRIEL WEATHERHEAD
  181083. 12835
  181084. JOCC?ELIEL AMINE CHIRAL NAPHTHYL RESOLUTION OPTICAL INDUCTION REVIEWM
  181085. 13844N
  181086. 2/28/96V:USE OF OPTICALLY ACTIVE NAPHTHYLETHYL AMINE FOR RESOLUTIONW
  181087. VOL 0   1983  PG 48a
  181088. GABRIEL WEATHERHEAD
  181089. 12836
  181090. HETEROCYCLESC#COUTTS REVIEW HYDROXYL AMINE CYCLICM
  181091. 13845N
  181092. 2/28/96VFCYCLIC HYDROXYLAMINES: A REVIEW OF PREPARATIVE METHODS AND PROPERTIES.W
  181093. VOL 0   1974  PG 689a
  181094. GABRIEL WEATHERHEAD
  181095. 12837
  181096. TETRAHEDRONC7GASC REVIEW AMINE ALCOHOL ALKENE PREPARATION CONVERSIONM
  181097. 13846N
  181098. 2/28/96V
  181099. AMINATION OF ALKENES
  181100. VOL 39   1983  PG 702a
  181101. GABRIEL WEATHERHEAD
  181102. 12838
  181103. TETRAHEDRONC+L'ABBE REVIEW SULFUR CONVERSION HETEROCYCLEM
  181104. 13847N
  181105. 2/28/96VDSOME RING TRANSFORMATION REACTIONS OF SULFUR CONTAINING HETEROCYCLESW
  181106. VOL 24   1982  PG 3537a
  181107. GABRIEL WEATHERHEAD
  181108. 12839
  181109. TETRAHEDRONC=CLIVE REVIEW SELENIUM UMPOLUNG METHODOLOGY ALKYLATION EPOXIDEM
  181110. 13848N
  181111. 2/28/96V
  181112. MODERN ORGANOSELENIUM CHEMISTRYW
  181113. VOL 34   1978  PG 1049a
  181114. GABRIEL WEATHERHEAD
  181115. 12840
  181116. HETEROCYCLESC=COOK SYNTHESIS AZINE HETEROCYCLE REVIEW AZAPHENALENE AROMATICM
  181117. 13849N
  181118. 2/28/96V
  181119. SYNTHESIS OF AZAPHENALENESW
  181120. VOL 20   1983  PG 87a
  181121. GABRIEL WEATHERHEAD
  181122. 12841
  181123. ANGEW CHEM INT ED ENGLCFHUISGEN DIPOLE VINYL ELECTROCYCLIC CYCLIZATION REVIEW ORBITAL SYMMETRYM
  181124. 13850N
  181125. 2/28/96V+1,5 ELECTROCYCLIZATION OF VINYL 1,3 DIPOLESW
  181126. VOL 19   1980  PG 946a
  181127. GABRIEL WEATHERHEAD
  181128. 12842
  181129. JOCCDMACDONALD ALKALOID NIH WRITING CANCER REVIEW PYRAZOLIDINE REFERENCESM
  181130. 13851N
  181131. 2/28/96
  181132. V.PYRROLIZIDINE ALKALOID SYNTHESIS OF SUPINIDINEW
  181133. VOL 48   1983  PG 1129a
  181134. GABRIEL WEATHERHEAD
  181135. 12843
  181136. JOCCPMASAMUNE CYCLOADDITION DIELS ALDER REVIEW INDUCTION ASYMMETRIC STEREOCHEM CHIRALM
  181137. 13852N
  181138. 2/28/96V=ASYMMETRIC DIELS ALDER REACTION: DESIGN OF CHIRAL DIENOPHILESW
  181139. VOL 48   1983  PG 1137a
  181140. GABRIEL WEATHERHEAD
  181141. 12844
  181142. B    SYNTHESISCNMITSUNOBU ALCOHOL DISPLACEMENT PHOSPHOROUS AZO CARBOXYLATE METHODOLOGY REAGENTM
  181143. 13853N
  181144. 2/28/96VSREVIEW OF THE MITSUNOBU REACTION INVOLVING TRIPHENYL PHOSPHINE AND AZODICARBOXYLATEW
  181145. VOL 0   1981  PG 1a
  181146. GABRIEL WEATHERHEAD
  181147. 12845
  181148. ANGEW CHEM INT ED ENGLCUL'ABBE REVIEW HETEROCYCLE CYCLOPROPANE HETEROCYCLE REARRANGEMENT SMALL RING CHEMISTRYM
  181149. 13854N
  181150. 2/28/96V0HETEROCYCLIC ANALOGUES OF METHYLANECYCLOPROPANESW
  181151. VOL 19   1980  PG 277a
  181152. GABRIEL WEATHERHEAD
  181153. 12846
  181154. ANGEW CHEM INT ED ENGLC=KAUP PHOTOREARRANGEMENT REVIEW BENZENE FRAGMENTATION AROMATICM
  181155. 13855N
  181156. 2/28/96
  181157. VZPHOTOCHEMICAL REARRANGEMENTS AND FRAGMENTATIONS OF BENZENE DERIVATIVE AND ANNELATED ARENESW
  181158. VOL 19   1980  PG 243a
  181159. GABRIEL WEATHERHEAD
  181160. 12847
  181161. ANGEW CHEM INT ED ENGLCHTURRO REVIEW ENERGY TRANSFER H ABSTRACTION DIMERIZATION PHOTOCHEM MICELLM
  181162. 13856N
  181163. 2/28/96V=PHOTOPHYSICAL AND PHOTOCHEMICAL PROCESSES IN MICELLAR SYSTEMSW
  181164. VOL 19   1980  PG 675a
  181165. GABRIEL WEATHERHEAD
  181166. 12848
  181167. ANGEW CHEM INT ED ENGLC:ADAM SYNTHESIS ALKANE DIAZO PHOTOCHEM THERMAL NOVEL REVIEWM
  181168. 13857N
  181169. 2/28/96V:THE SYNTHESIS OF UNUSUAL ORGANIC MOLECULES FROM AZOALKANESW
  181170. VOL 19   1980  PG 760a
  181171. GABRIEL WEATHERHEAD
  181172. 12849
  181173. ANGEW CHEM INT ED ENGLCZSTEGELMEIER AZEPINE SYNTHESIS SPECTROSCOPY SUBSTITUTION AROMATICITY TAUTOMERIZATION REVIEWM
  181174. 13858N
  181175. 2/28/96V<1FH AZEPINE  NMR SPECTROSCOPIC AND CHEMICAL CHARACTERIZATIONW
  181176. VOL 19   1980  PG 1016a
  181177. GABRIEL WEATHERHEAD
  181178. 12850
  181179. ANGEW CHEM INT ED ENGL
  181180. COCHRISTL SYNTHESIS SPECTROSCOPY PHOTOREARRANGEMENT BENZVALENE REVIEW PREPARATIONM
  181181. 13859N
  181182. 2/28/96V,BENVALENE PROPERTIES AND SYNTHETIC POTENTIALW
  181183. VOL 20   1981  PG 530a
  181184. GABRIEL WEATHERHEAD
  181185. 12851
  181186. HETEROCYCLESCGELNAGDI NITRILE HETEROCYCLE SYNTHESIS REAGENT REVIEW UNSATURATED ALKENEM
  181187. 13860N
  181188. 2/28/96V:UTILITY OF UNSATURATED NITRILES IN HETEROCYCLIC SYNTHESIS.W
  181189. VOL 20   1983  PG 519a
  181190. GABRIEL WEATHERHEAD
  181191. 12852
  181192. TETRAHEDRONC^KELLOGG DIPOLE AZOMETHINE YLIDE CARBONYL YLIDE THIOCARBONYL YLIDE CYCLOADDITION REVIEW WRITINGM
  181193. 13861N
  181194. 2/28/96VWGENERATION OF AZOMETHINE CARBONYL AND THIOCARBONYL YLIDES. THEIR SYNTHESES, PROPERTIES,W
  181195. VOL 32   1976  PG 2165a
  181196. GABRIEL WEATHERHEAD
  181197. 12853
  181198. TETRAHEDRONCGOLAH REAGENT REVIEW SILICON TRIMETHYL SILYL IODIDE CLEAVAGE ESTER ETHERM
  181199. 13862N
  181200. 2/28/96V<IODOTRIMETHYLSILANE A VERSATILE SYNTHETIC REAGENT A OVERVIEWW
  181201. VOL 0   1982  PG 2225a
  181202. GABRIEL WEATHERHEAD
  181203. 12854
  181204. TETRAHEDRON
  181205. CLRAMSDEN MESOIONIC HETEROCYCLE ZWITTERION DIPOLE CYCLOADDITION REVIEW SYDNONEM
  181206. 13863N
  181207. 2/28/96V0MEROIONIC HETEROCYCLES FROM 1976 1980. A REVIEW.W
  181208. VOL 38   1982  PG 2964a
  181209. GABRIEL WEATHERHEAD
  181210. 12855
  181211. TETRAHEDRONCMWEINREB DIELS ALDER REVIEW HETEROCYCLE IMINE CARBONYL CYCLOADDITION SYNTHESISM
  181212. 13864N
  181213. 2/28/96VFSYNTHETIC ASPECTS OF DIELS ALDER CYCLOADDITIONS WITH HETERODIENOPHILESW
  181214. VOL 38   1982  PG 3087a
  181215. GABRIEL WEATHERHEAD
  181216. 12856
  181217. TETRAHEDRONCAWERSTIUK REVIEW HOMO ENOLATE HOMOENOLATE ANION MECHANISM UMPOLUNGM
  181218. 13865N
  181219. 2/28/96VaHOMOLATE ANIONS AND HOMOENOLATE ANION EQUIVALENTS, MECHANISTIC ASPECTS AND SYNTHETIC APPLICATIONSW
  181220. VOL 39   1983  PG 205a
  181221. GABRIEL WEATHERHEAD
  181222. 12857
  181223. B    CHEM LETTC3YAMADA NIH ALKALOID SYNTHESIS CANCER WRITING REVIEWM
  181224. 13866N
  181225. 2/28/96VLA CONVENIENT SYNTHESIS OF RETRONECINE A MEMBER OF THE PYRROLIZIDINE ALKOLOIDW
  181226. VOL 0   1983  PG 128a
  181227. GABRIEL WEATHERHEAD
  181228. 12858
  181229. B    SYNTHESIS
  181230. CBPETRAGNANI ANION DIANION ACID ESTER ALKYLATION EXPERIMENTAL REVIEWM
  181231. 13867N
  181232. 2/28/96VFREACTIONS OF DIANIONS OF CARBOXYLIC ACIDS AND ESTER ENOLATES. A REVIEWW
  181233. VOL 0   1982  PG 521a
  181234. GABRIEL WEATHERHEAD
  181235. 12859
  181236. B    SYNTHESISC5BROWNBRIDGE ENOL ETHER SILICON SILYL REVIEW CHEMISTRYM
  181237. 13868N
  181238. 2/28/96V/SILYL ENOL ETHER IN ORGANIC SYNTHESIS. A REVIEWW
  181239. VOL 0   1983  PG 20a
  181240. GABRIEL WEATHERHEAD
  181241. 12860
  181242. CHEM SOC REVCCAGER SILICON REVIEW ALKENE EQUIVALENT ALKYLATION CARBANION UMPOLUNGM
  181243. 13869N
  181244. 2/28/96V'SILICON CONTAINING CARBONYL EQUIVALENTSW
  181245. VOL 0   1982  PG 493a
  181246. GABRIEL WEATHERHEAD
  181247. 12861
  181248. ACCT CHEM RESCDBARRETT TOSYLHYDRAZONE SHAPIRO HYDRAZONE NAME VINYL CARBANION REVIEWM
  181249. 13870N
  181250. 2/28/96V*RECENT APPLICATIONS OF THE SHANRO REACTIONW
  181251. VOL 16   1983  PG 55a
  181252. GABRIEL WEATHERHEAD
  181253. 12862
  181254. B    SYNTHESISC8BHATT ETHER CLEAVAGE REAGENT REVIEW SILANE SILYL SILICONM
  181255. 13871N
  181256. 2/28/96V'CLEAVAGE OF ETHERS IN ORGANIC SYNTHESISW
  181257. VOL 0   1983  PG 249
  181258. GABRIEL WEATHERHEAD
  181259. 12863
  181260. ALDRICH CHIM ACTAC0BLACK DIAZO DIAZOMETHANE REVIEW REAGENT REACTIONM
  181261. 13872N
  181262. 2/28/96V-THE PREPARATION AND REACTIONS OF DIAZOMETHANEW
  181263. VOL 16   1983  PG 1a
  181264. GABRIEL WEATHERHEAD
  181265. 12864
  181266. ALDRICH CHIM ACTAC@STANG TRIFLATE TRIFLIC FLUORINE SULFONYL REACTION REVIEW REAGENTM
  181267. 13873N
  181268. 2/28/96V TRIFLIC ACID AND ITS DERIVATIVESW
  181269. VOL 16   1983  PG 15a
  181270. GABRIEL WEATHERHEAD
  181271. 12865
  181272. JOCC;WENZEL REVIEW NMR SPECTROSCOPY SHIFT REAGENT METAL EUROPIUMM
  181273. 13874N
  181274. 2/28/96V,NMR SHIFT REAGENTS FOR OLEFINS AND AROMATICSW
  181275. VOL 48   1983  PG 1951a
  181276. GABRIEL WEATHERHEAD
  181277. 12866
  181278. JOCC:SNIDER ENE LEWIS ACID ENONE ALUMINUM ACRYLATE ESTER REVIEWM
  181279. 13875N
  181280. 2/28/96V5SEQUENTIAL ENE REACTIONS. A NEW ANNELACTION PROCEDUREW
  181281. VOL 48   1983  PG 1822a
  181282. GABRIEL WEATHERHEAD
  181283. 12867
  181284. TETRAHEDRONC<BRINKMEYER REVIEW ACETAL FORMAMIDE DMF CONDENSATION ADDITIONM
  181285. 13876N
  181286. 2/28/96V(REVIEW OF CHEMISTRY OF FORMAMIDE ACETALS
  181287. VOL 35   1979  PG 1675a
  181288. GABRIEL WEATHERHEAD
  181289. 12868
  181290. ACCT CHEM RESC8KWART TEMPERATURE REVIEW ENE ISOTOPE DEUTERIUM MECHANISMM
  181291. 13877N
  181292. 2/28/96VVTEMPERATURE DEPENDENCE OF THE PRIMARY KINETIC ISOTOPE EFFECT AS A MECHANISTIC CRITERIAW
  181293. VOL 15   1982  PG 401a
  181294. GABRIEL WEATHERHEAD
  181295. 12869
  181296. TETRAHEDRONCDWIESNER STEREOCHEM PHOTOCYCLOADDITION NONE ALKENE CYCLOBUTANE REVIEWM
  181297. 13878N
  181298. 2/28/96VOON THE STEREOCHEMISTRY OF PHOTOADDITION BETWEEN UNSATURATED KETONES AND OLEFINSW
  181299. VOL 36   1980  PG 719a
  181300. GABRIEL WEATHERHEAD
  181301. 12870
  181302. TETRAHEDRONCIBECKER ALKENE CYCLOALKENE KETONE WITTIG INTRAMOLECULAR REVIEW PHOSPHOROUSM
  181303. 13879N
  181304. 2/28/96V.CYCLOALKENES BY INTRAMOLECULAR WITTIG REACTIONW
  181305. VOL 36   1980  PG 1717a
  181306. GABRIEL WEATHERHEAD
  181307. 12871
  181308. TETRAHEDRONCFBARRETT REVIEW CHEMISTRY THIAZOLINE HETEROCYCLE SULFUR TAUTOMERIZATIONM
  181309. 13880N
  181310. 2/28/96VBTHE CHEMISTRY OF 1,3 THIAZOLINONE AND HYDROXY 1,3 THIAZOLE SYSTEMSW
  181311. VOL 36   1980  PG 2023
  181312. GABRIEL WEATHERHEAD
  181313. 12872
  181314. TETRAHEDRONCLFUSCO HYDRAZINE HYDRAZIDOYL CHLORIDE SIGMATROPIC REARRANGEMENT INDOLE REVIEWM
  181315. 13881N
  181316. 2/28/96VbN N BOND CLEAVAGE AND REARRANGEMENTS OF ARYLHYDRAZONES AND ARYL  HYDRAZIDES   RECENT DEVELOPEMENTSW
  181317. VOL 36   1980  PG 161a
  181318. GABRIEL WEATHERHEAD
  181319. 12873
  181320. TETRAHEDRONCINEWTON HETEROCYCLE FIVE RING MESOIONIC REVIEW DIPOLE ZWITTERION MUNCHNONEM
  181321. 13882N
  181322. 2/28/96V*MESO IONIC HETEROCYCLES (1976 1980 REVIEW)W
  181323. VOL 38   1982  PG 2965a
  181324. GABRIEL WEATHERHEAD
  181325. 12874
  181326. TETRAHEDRONC/WILSON REVIEW SULFUR SULFONIUM PUMMERER HALOGENM
  181327. 13883N
  181328. 2/28/96V/STRUCTURE AND REACTIVITY OF HALOSULFONIUM SALTSW
  181329. VOL 38   1982  PG 2597a
  181330. GABRIEL WEATHERHEAD
  181331. 12875
  181332. TETRAHEDRONCQHICKMOTT REVIEW ENAMINE PREPARATION SPECTROSCOPY ALKYLATION REACTIVITY STEREOCHEMM
  181333. 13884N
  181334. 2/28/96V\ENAMINES: RECENT ADVANCES IN SYNTHETIC, SPECTROSCOPIC, MECHANISTICAND STEREOCHEMICAL ASPECTSW
  181335. VOL 38   1982  PG 1975a
  181336. GABRIEL WEATHERHEAD
  181337. 12876
  181338. B    SYNTHESISCBDEEM DIPOLAR CYCLOADDITION CYCLOPROPENE REVIEW STRAIN ADDITION 2+2M
  181339. 13885N
  181340. 2/28/96V~EXPANDED RING SYSTEMS FROM CYCLOPROPENES; 1,3 DIPOLAR AND [2+2]  ADDITIONS ACROSS THE CYCLOPROPENYL   BOND, (A REVIEW ARTICLE)W
  181341. VOL 0   1982  PG 701a
  181342. GABRIEL WEATHERHEAD
  181343. 12877
  181344. ACCT CHEM RESCJSCHULTZ PHOTOREARRANGEMENT CYCLIZATION ELECTROCYCLIC YLIDE TRAPPING REVIEWM
  181345. 13886N
  181346. 2/28/96V6PHOTOCHEMICAL SIX ELECTRON HETEROCYCLIZATION REACTIONSW
  181347. VOL 16   1983  PG 210a
  181348. GABRIEL WEATHERHEAD
  181349. 12878
  181350. B    SYNTHESISCCDEMUTH REVIEW TRIFLATE SILICON ALKYLATION PREPARATION REAGENT SILYLM
  181351. 13887N
  181352. 2/28/96VZA CONVENIENT IN SITU PREPARATION OF TRIMETHYLSILYL TRIFLUORO  METHANE SULFONATE [SEE CARD]W
  181353. VOL 0   1982  PG 827a
  181354. GABRIEL WEATHERHEAD
  181355. 12879
  181356. ACCT CHEM RESCPZIEGLER REVIEW CLAISEN REARRANGEMENT REGIOCHEM STEREOCHEM NATURAL PRODUCT TARGETM
  181357. 13888N
  181358. 2/28/96
  181359. VbSTEREO  AND REGIOCHEMISTRY OF THE CLAISEN REARRANGEMENT:APPLICA  TION TO NATURAL PRODUCT SYNTHESISW
  181360. VOL 10   1977  PG 227a
  181361. GABRIEL WEATHERHEAD
  181362. 12880
  181363. B    SYNTHESISCABENNETT REVIEW CLAISEN SIGMATROPIC REARRANGEMENT ORBITAL SYMMETRYM
  181364. 13889N
  181365. 2/28/96V1THE CLAISEN REARRANGEMENT IN ORG. SYN., 1967 1977W
  181366. VOL 0   YR[67]   PG 589a
  181367. GABRIEL WEATHERHEAD
  181368. 12881
  181369. ANGEW CHEM INT ED ENGLC8OPPOLZER REVIEW DIELS ALDER DIPOLAR CYCLOADDITION DIPOLEM
  181370. 13890N
  181371. 2/28/96VBINTRAMOLECULAR [4+2] AND [3+2] CYCLOADDITIONS IN ORGANIC SYNTHESISW
  181372. VOL 16   1977  PG 10a
  181373. GABRIEL WEATHERHEAD
  181374. 12882
  181375. ANGEW CHEM INT ED ENGLC;POMMER REVIEW WITTIG ALKYLATION PHOSPHOROUS INDUSTRY ALKENEM
  181376. 13891N
  181377. 2/28/96V3THE WITTIG REACTION IN INDUSTRIAL PRACTICE (REVIEW)W
  181378. VOL 16   1977  PG 423a
  181379. GABRIEL WEATHERHEAD
  181380. 12883
  181381. B    SYNTHESISCBBROWN BORON REVIEW BROWN HYDROBORATION ORGANOBORANE ALKENE ALCOHOLM
  181382. 13892N
  181383. 2/28/96V&REVIEWS ON BORANE CHEMISTRY (SEE CARD)W
  181384. VOL 0   1977  PG 695
  181385. GABRIEL WEATHERHEAD
  181386. 12884
  181387. CHEM SOC REVCBLEE RUFF SUPEROXIDE REVIEW OXYGEN SINGLET OXYGEN ELECTRON TRANSFERM
  181388. 13893N
  181389. 2/28/96V
  181390. SUPEROXIDE REVIEWW
  181391. VOL 6   1977  PG 195a
  181392. GABRIEL WEATHERHEAD
  181393. 12885
  181394. FORTSCHRITTE DER CHEM FORSCHUNGCHWENTRUP REVIEW REARRANGEMENT REACTIVE INTERMEDIATE CARBENE NITRENE FLASHM
  181395. 13894N
  181396. 2/28/96V<REARRANGEMENTS AND INTERCONVERSIONS OF CARBENES AND NITRENESW
  181397. VOL 62   1976  PG 173a
  181398. GABRIEL WEATHERHEAD
  181399. 12886
  181400. TETRAHEDRONC>FICINI REVIEW YNAMINE SYNTHESIS INTERMEDIATE CYCLOADDITION 2+2M
  181401. 13895N
  181402. 2/28/96V.YNAMINE: A VERSATILE TOOL IN ORGANIC SYNTHESISW
  181403. VOL 32   1976  PG 1449a
  181404. GABRIEL WEATHERHEAD
  181405. 12887
  181406. CHEM REVCbSPANGLER SIGMATROPIC REARRANGEMENT THERMAL REVIEW ORBITAL SYMMETRY MOLECULAR ORBITAL ELECTROCYCLICM
  181407. 13896N
  181408. 2/28/96V(THERMAL [1,j] SIGMATROPIC REARRANGEMENTSW
  181409. VOL 76   1976  PG 187a
  181410. GABRIEL WEATHERHEAD
  181411. 12888
  181412. TETRAHEDRON
  181413. CGD'ANGELO REVIEW ALKYLATION KETONE METHODOLOGY EXPERIMENTAL ENOLATE ENOLM
  181414. 13897N
  181415. 2/28/96V=KETONE ENOLATES: REGIOSPECIFIC PREPARATION AND SYNTHETIC USESW
  181416. VOL 32   1976  PG 2979a
  181417. GABRIEL WEATHERHEAD
  181418. 12889
  181419. PURE AND APPL CHEMCDBESTMANN WITTIG REVIEW STEREOCHEM MECHANISM PHOSPHOROUS YLIDE ALKENEM
  181420. 13898N
  181421. 2/28/96V,SYNTHESIS OF POLYENES VIA PHOSPHONIUM YLIDESW
  181422. VOL 51   1979  PG 515a
  181423. GABRIEL WEATHERHEAD
  181424. 12890
  181425. B    SYNTHESISCCFLEMING REVIEW SILICON SILANE ALKENE EQUIVALENT REAGENT METHODOLOGYM
  181426. 13899N
  181427. 2/28/96VxALLYLSILANES IN ORGANIC SYNTHESIS: A METHOD FOR THE INTRODUC  TION OF TWO CARBON SUBSTITUENTS IN PACE OF CARBONYL OXYGENW
  181428. VOL 0   1979  PG 446a
  181429. GABRIEL WEATHERHEAD
  181430. 12891
  181431. UNKNOWNCAHAJOS ALDOL CONDENSATION METHODOLOGY REVIEW ALDEHYDE EXPERIMENTALM
  181432. 13900N
  181433. 2/28/96V5ALDOL CONDENSATIONS   PROCEDURES AVAILABLE (SEE CARD)W
  181434. VOL 1   1979  PG 1a
  181435. GABRIEL WEATHERHEAD
  181436. 12892
  181437. TET LETT
  181438. C<YAMAMOTO EXPERIMENTAL MICHAEL NAME CONJUGATE ADDITION REVIEWM
  181439. 13901N
  181440. 2/28/96V*15 METHODS FOR MICHAEL ADDITION (SEE CARD)W
  181441. VOL 0   1982  PG 3711a
  181442. GABRIEL WEATHERHEAD
  181443. 12893
  181444. TETRAHEDRONCZKAMETANI REVIEW BENZOCYCLOBUTENE QUINONE METHIDE STEROID TARGET INTRAMOLECULAR DIELS ALDERM
  181445. 13902N
  181446. 2/28/96VaUSE OF BENZOCYCLOBUTENES AND INTRAMOLECULAR DIELS ALDER REACTION FOR STEROID SYNTHESIS (SEE CARD)W
  181447. VOL 37   1981  PG 31a
  181448. GABRIEL WEATHERHEAD
  181449. 12894
  181450. ALDRICH CHIM ACTACGHASE UMPOLUNG REVIEW EQUIVALENT CARBANION ALKYLATION METHODOLOGY SULFURM
  181451. 13903N
  181452. 2/28/96V?A COMPILATION OF REFERENCES ON R FUNCTIONAL ACYL ANION SYNTHONSW
  181453. VOL 15   1982  PG 35a
  181454. GABRIEL WEATHERHEAD
  181455. 12895
  181456. UNKNOWNC<STANG ALKENE VINYL CATION TRIFLATE REVIEW BOOK REARRANGEMENTM
  181457. 13904N
  181458. 2/28/96V
  181459. VINYL CATIONSW
  181460. VOL 0   1979  PG 20a
  181461. GABRIEL WEATHERHEAD
  181462. 12896
  181463. UNKNOWNC@NEGISHI ORGANOMETALLIC REVIEW LITHIUM GRIGNARD SYNTHESIS LITHIUMM
  181464. 13905N
  181465. 2/28/96
  181466. V$ORGANOMETALLICS IN ORGANIC SYNTHESISW
  181467. VOL 1   1980  PG 0a
  181468. GABRIEL WEATHERHEAD
  181469. 12897
  181470. HETEROCYCLESCEWEINREB DIELS ALDER REVIEW HETEROCYCLE AZA IMINE CYCLOADDITION TARGETM
  181471. 13906N
  181472. 2/28/96VOSYNTHESIS OF NITROGEN CONTAINING HETEROCYCLES BY THE IMINO DIELS ALDER REACTIONW
  181473. VOL 12   1979  PG 949a
  181474. GABRIEL WEATHERHEAD
  181475. 12898
  181476. HETEROCYCLESCKABOU GHARBIA NITRONE DIPOLAR CYCLOADDITION DIPOLE KETENE HETEROCYCLE REVIEWM
  181477. 13907N
  181478. 2/28/96V"REACTIONS OF NITRONES WITH KETENESW
  181479. VOL 12   1979  PG 819a
  181480. GABRIEL WEATHERHEAD
  181481. 12899
  181482. ORGANIC PHOTOCHEMC7HIXSON CYCLOPROPANE PHOTOREARRANGEMENT DIRADICAL REVIEWM
  181483. 13908N
  181484. 2/28/96V
  181485. PHOTOCHEMISTRY OF CYCLOPROPANESW
  181486. VOL 4   1979  PG 0a
  181487. GABRIEL WEATHERHEAD
  181488. 12900
  181489. ADV HETERO CHEMC>WAKEFIELD ISOXAZOLE REVIEW CHEMISTRY NIH BIOLOGY REARRANGEMENTM
  181490. 13909N
  181491. 2/28/96V
  181492. ISOXAZOLE CHEMISTRY SINCE 1963W
  181493. VOL 25   1979  PG 147a
  181494. GABRIEL WEATHERHEAD
  181495. 12901
  181496. ORG REACTIONS
  181497. CMGSCHWEND LITHIUM CARBANION HETEROCYCLE REVIEW ALKYLATION EXPERIMENTAL LITHIUMM
  181498. 13910N
  181499. 2/28/96V"HETEROATOM FACILITATED LITHIATIONSW
  181500. VOL 26   1979  PG 1a
  181501. GABRIEL WEATHERHEAD
  181502. 12902
  181503. ORG REACTIONSCIGRIECO DIAZO KETONE CATALYST INTRAMOLECULAR CYCLOADDITION REVIEW ADDITIONM
  181504. 13911N
  181505. 2/28/96V3INTRAMOLECULAR REACTIONS OF DIAZOCARBONYL COMPOUNDSW
  181506. VOL 26   1979  PG 361a
  181507. GABRIEL WEATHERHEAD
  181508. 12903
  181509. CHEM INDC?MCOMIE PROTECTION DEPROTECTION REVIEW CARBONYL ACID DIENE AMINEM
  181510. 13912N
  181511. 2/28/96V*RECENT DEVELOPMENTS WITH PROTECTING GROUPSW
  181512. VOL 0   1979  PG 603a
  181513. GABRIEL WEATHERHEAD
  181514. 12904
  181515. CHEM & INDCIHASLAM ACID PARAMETER CONVERSION ESTER METHODOLOGY REVIEW CARBOXYLIC ACIDM
  181516. 13913N
  181517. 2/28/96V/ACTIVATION AND PROTECTION OF THE CARBOXYL GROUPW
  181518. VOL 0   1979  PG 610a
  181519. GABRIEL WEATHERHEAD
  181520. 12905
  181521. ANGEW CHEM INT ED ENGLCMMETH COHN REVIEW NITRENE AROMATIC CYCLIZATION MULTIPLICITY INSERTION ADDITIONM
  181522. 13914N
  181523. 2/28/96
  181524. V?DEVELOPMENTS IN ARYLNITRENE CHEMISTRY: SYNTHESES AND MECHANISMSW
  181525. VOL 18   1979  PG 900a
  181526. GABRIEL WEATHERHEAD
  181527. 12906
  181528. ANGEW CHEM INT ED ENGLCIBIANCHI CYCLOREVERSION REVIEW DIPOLE DIPOLAR AZIDE DIAZO AZOMETHINE YLIDEM
  181529. 13915N
  181530. 2/28/96V
  181531. 1,3 DIPOLAR CYCLOREVERSIONSW
  181532. VOL 18   1979  PG 72a
  181533. GABRIEL WEATHERHEAD
  181534. 12907
  181535. ANGEW CHEM INT ED ENGLCFMUKAIYAMA CONVERSION ACID ALCOHOL ESTER HETEROCYCLE METHODOLOGY REVIEWM
  181536. 13916N
  181537. 2/28/96V>NEW SYNTHETIC REACTIONS BASED ON THE ONIUM SALTS OF AZA ARENESW
  181538. VOL 18   1979  PG 707a
  181539. GABRIEL WEATHERHEAD
  181540. 12908
  181541. ANGEW CHEM INT ED ENGLCCTURRO THEORY PHOTOCHEM ADIABATIC REVIEW PHYSICAL ORGANIC SENSITIZERM
  181542. 13917N
  181543. 2/28/96V-ADIABATIC PHOTOREACTIONS OF ORGANIC MOLECULESW
  181544. VOL 18   1979  PG 572a
  181545. GABRIEL WEATHERHEAD
  181546. 12909
  181547. ANGEW CHEM INT ED ENGLCYHOFFMANN REVIEW SIGMATROPIC THEORY ORBITAL SYMMETRY HETEROCYCLE HETEROCYCLE REARRANGEMENTM
  181548. 13918N
  181549. 2/28/96V3STEREOCHEMISTRY OF [2,3] SIGMATROPIC REARRANGEMENTS
  181550. VOL 18   1979  PG 563a
  181551. GABRIEL WEATHERHEAD
  181552. 12910
  181553. ACCT CHEM RESCHTUFARIELLO REVIEW NITRONE ALKALOID SYNTHESIS TARGET DIPOLE CYCLOADDITIONM
  181554. 13919N
  181555. 2/28/96V
  181556. ALKALOIDS FROM NITRONESW
  181557. VOL 0   YR[0]   PG 0a
  181558. GABRIEL WEATHERHEAD
  181559. 12911
  181560. ACCT CHEM RESCLMORRISON REVIEW BICHROMOPHORE CARBONYL KETONE PHOTOCHEM ALKENE ISOMERIZATIONM
  181561. 13920N
  181562. 2/28/96V2PHOTOCHEMISTRY OF ORGANIC BICHROMOPHORIC MOLECULESW
  181563. VOL 12   1979  PG 383a
  181564. GABRIEL WEATHERHEAD
  181565. 12912
  181566. ACCT CHEM RESCBSCHAEFER REVIEW MIGRATION SIGMATROPIC CARBENE NITRENE VINYL ALKENEM
  181567. 13921N
  181568. 2/28/96V]THE 1,2 HYDROGEN SHIFT: A COMMON VEHICLE FOR THE DISAPPEARANCE OF EVANESCENT MOLECULAR SECIESW
  181569. VOL 12   1979  PG 288a
  181570. GABRIEL WEATHERHEAD
  181571. 12913
  181572. B    SYNTHESISCFMARTIN REVIEW ALDEHYDE KETONE COUPLING TITANIUM CARBANION DIMERIZATIONM
  181573. 13922N
  181574. 2/28/96VlSYNTHESIS OF ALDEHYDES, KETONES AND CARBOXYLIC ACIDS FROM LOWER CARBONYL COMPOUNDS BY C C COUPLING REACTIONSW
  181575. VOL 0   1979  PG 633
  181576. GABRIEL WEATHERHEAD
  181577. 12914
  181578. B    SYNTHESISCHMATHIAS REVIEW CONVERSION ACID ESTER CATALYST DEHYDROGENATION ALKYLATIONM
  181579. 13923N
  181580. 2/28/96V;ESTERIFICATIONS AND ALKYLATION REACTIONS EMPLOYING ISOUREASW
  181581. VOL 0   1979  PG 561a
  181582. GABRIEL WEATHERHEAD
  181583. 12915
  181584. TETRAHEDRONCLVIOLA REVIEW FLASH ALKYNE ELECTROCYCLIC INTRAMOLECULAR CARBENE REARRANGEMENTM
  181585. 13924N
  181586. 2/28/96V;INTRAMOLECULAR PERICYCLIC REACTIONS OF ACETYLENIC COMPOUNDSW
  181587. VOL 37   1981  PG 3764a
  181588. GABRIEL WEATHERHEAD
  181589. 12916
  181590. IND ENG CHEM PROD RES DEVCPTURCHI HETEROCYCLE REVIEW OXAZOLE REACTION HETEROCYCLE REARRANGEMENT PREPARATIONM
  181591. 13925N
  181592. 2/28/96V.OXAZOLE CHEMISTRY. A REVIEW OF RECENT ADVANCESW
  181593. VOL 20   1981  PG 32a
  181594. GABRIEL WEATHERHEAD
  181595. 12917
  181596. ACCT CHEM RESCRSTEPHENSON ENE MECHANISM ISOTOPE EFFECT STEREOCHEM REGIOCHEM SINGLET OXYGEN REVIEWM
  181597. 13926N
  181598. 2/28/96V@MECHANISM OF THE ENE REACTION BETWEEN SINGLET OXYGEN AND OLEFINSW
  181599. VOL 13   1980  PG 419a
  181600. GABRIEL WEATHERHEAD
  181601. 12918
  181602. ACCT CHEM RESCDSNIDER ENE MECHANISM STEREOCHEM REGIOCHEM CATALYST LEWIS ACID REVIEWM
  181603. 13927N
  181604. 2/28/96V"LEWIS ACID CATALYZED ENE REACTIONSW
  181605. VOL 13   1980  PG 426a
  181606. GABRIEL WEATHERHEAD
  181607. 12919
  181608. ACCT CHEM RESC@HEGARTY NITRILE DIPOLE IMINE DIPOLAR NITRILIUM ALKYLATION REVIEWM
  181609. 13928N
  181610. 2/28/96VDSTEREOSPECIFIC REACTION OF NITRILIUM IONS AND ANALOGOUS 1,3  DIPOLESW
  181611. VOL 13   1980  PG 448a
  181612. GABRIEL WEATHERHEAD
  181613. 12920
  181614. B$NEW TRENDS IN HETEROCYCLIC CHEMISTRYCHREES AZETE CYCLOADDITION HETEROCYCLE REVIEW BENZAZETE EXTRUSION NITROGENM
  181615. 13929N
  181616. 2/28/96V
  181617. THE CHEMISTRY OF BENZAZETESW
  181618. VOL 0   1979  PG 356a
  181619. GABRIEL WEATHERHEAD
  181620. 12921
  181621. ACCT CHEM RESCWBOEKELHEIDE CYCLOPHANE CYCLOADDITION SYNTHESIS METHODOLOGY O XYLENE DIMERIZATION REVIEWM
  181622. 13930N
  181623. 2/28/96V.[2N]CYCLOPHANES: PARACYCLOPHANES TO SUPERPHANEW
  181624. VOL 13   1980  PG 65a
  181625. GABRIEL WEATHERHEAD
  181626. 12922
  181627. ACCT CHEM RES
  181628. CXTHUMMEL BENZOCYCLOBUTENE EXTRUSION CYCLOADDITION SYNTHESIS SULFONE SULFUR DIOXIDE REVIEWM
  181629. 13931N
  181630. 2/28/96V'BENZOCYCLOBUTENES AND RELATED COMPOUNDSW
  181631. VOL 13   1980  PG 70a
  181632. GABRIEL WEATHERHEAD
  181633. 12923
  181634. B$NEW TRENDS IN HETEROCYCLIC CHEMISTRYCYKATRITSKY AZOMETHINE YLIDE PYRIDINIUM DIPOLAR CYCLOADDITION HETEROCYCLE ZWITTERION REVIEWM
  181635. 13932N
  181636. 2/28/96VdRECENT PROGRESS IN THE CYCLOADDITION REACTIONS OF 3 OXIDO  PYRIDINIUM BETAINES & ANALOGOUS COMPOUNDSW
  181637. VOL 0   1979  PG 290a
  181638. GABRIEL WEATHERHEAD
  181639. 12924
  181640. B$NEW TRENDS IN HETEROCYCLIC CHEMISTRYCHDITTMER CYCLOBUTENE SULFUR THIETE SYNTHESIS HETEROCYCLE FOUR RING REVIEWM
  181641. 13933N
  181642. 2/28/96VCCHEMISTRY OF THIACYCLOBUTENES (THIETES) AND THEIR VALENCE TAUTOMERSW
  181643. VOL 0   1979  PG 130a
  181644. GABRIEL WEATHERHEAD
  181645. 12925
  181646. ADV HETERO CHEMCDRAMSDEN DIPOLE CYCLOADDITION ZWITTERION HETEROCYCLE MESOIONIC REVIEWM
  181647. 13934N
  181648. 2/28/96V9HETEROCYCLIC BETAIN DERIVATIVES OF ALTERNATE HYDROCARBONSW
  181649. VOL 26   1980  PG 3a
  181650. GABRIEL WEATHERHEAD
  181651. 12926
  181652. ANGEW CHEM INT ED ENGLC:ADAM AZO ALKANE STRAIN NITROGEN EXTRUSION DIRADICAL REVIEWM
  181653. 13935N
  181654. 2/28/96V;THE SYNTHESIS OF UNUSUAL ORGANIC MOLECULES FROM AZO ALKANESW
  181655. VOL 19   1980  PG 762a
  181656. GABRIEL WEATHERHEAD
  181657. 12927
  181658. ANGEW CHEM INT ED ENGLCRSUKUMARAN PHOTOCYCLOADDITION HETEROCYCLE DIELS ALDER CYCLIZATION HEXATRIENE REVIEWM
  181659. 13936N
  181660. 2/28/96V\THERMAL AND PHOTOCHEMICAL TRANSFORMATIONS OF HETERO 1,3,5  HEXATRIENES INTO 5 MEMBERED RINGSW
  181661. VOL 19   1980  PG 973a
  181662. GABRIEL WEATHERHEAD
  181663. 12928
  181664. TETRAHEDRONC>SHEA CYCLOALKENE STRAIN BREDT THEORY DIELS ALDER REVIEW ALKENEM
  181665. 13937N
  181666. 2/28/96VSRECENT DEVELOPMENTS IN THE SYNTHESIS, STRUCTURE AND CHEMISTRY OF BRIDGEHEAD ALKENESW
  181667. VOL 36   1980  PG 1683a
  181668. GABRIEL WEATHERHEAD
  181669. 12929
  181670. ADV HETERO CHEMC>GRIMMETT IMIDAZOLE PREPARATION REVIEW SPECTROSCOPY HETEROCYCLEM
  181671. 13938N
  181672. 2/28/96V
  181673. ADVANCES IN IMIDAZOLE CHEMISTRYW
  181674. VOL 27   1980  PG 241a
  181675. GABRIEL WEATHERHEAD
  181676. 12930
  181677. TETRAHEDRONCGRAJAPPA ENAMINE NITRO PREPARATION DIELS ALDER HETEROCYCLE ALKENE REVIEWM
  181678. 13939N
  181679. 2/28/96V(NITROENAMINES   USE IN ORGANIC SYNTHESISW
  181680. VOL 0   1981  PG 1453a
  181681. GABRIEL WEATHERHEAD
  181682. 12931
  181683. TETRAHEDRONCRKATRITSKY AMINE LEAVING GROUP METHODOLOGY REVIEW DISPLACEMENT ELIMINATION PYRYLIUMM
  181684. 13940N
  181685. 2/28/96VUCONVERSION OF PRIMARY AMINE INTO OTHER FUNCTIONAL GROUPS MEDIATED BY PYRYLIUM CATIONSW
  181686. VOL 36   1980  PG 679a
  181687. GABRIEL WEATHERHEAD
  181688. 12932
  181689. B$NEW TRENDS IN HETEROCYCLIC CHEMISTRYCPHASSNER AZIRINE NITRILE YLIDE DIPOLAR CYCLOADDITION SYNTHESIS REVIEW HETEROCYCLEM
  181690. 13941N
  181691. 2/28/96V#RECENT ASPECTS OF AZIRINE CHEMISTRYW
  181692. VOL 0   1979  PG 178a
  181693. GABRIEL WEATHERHEAD
  181694. 12933
  181695. TETRAHEDRONCESONNET INVERSION ALKENE ISOMERIZATION EQUILIBRATION STEREOCHEM REVIEWM
  181696. 13942N
  181697. 2/28/96V#OLEFIN INVERSION OF Z AND E ISOMERSW
  181698. VOL 36   1980  PG 557a
  181699. GABRIEL WEATHERHEAD
  181700. 12934
  181701. CHEM REV
  181702. C@ENGEL AZO EXTRUSION MECHANISM COUPLING NITROGEN DIRADICAL REVIEWM
  181703. 13943N
  181704. 2/28/96VFMECHANISM OF THE THERMAL & PHOTOCHEMICAL DECOMPOSITION OF AZO  ALKENESW
  181705. VOL 2   1980  PG 80a
  181706. GABRIEL WEATHERHEAD
  181707. 12935
  181708. CHEM REVCVBRIEGER DIELS ALDER INTRAMOLECULAR CYCLOADDITION SYNTHESIS REGIOCHEM STEREOCHEM REVIEWM
  181709. 13944N
  181710. 2/28/96V$INTRAMOLECULAR DIELS ALDER REACTIONSW
  181711. VOL 80   1980  PG 63a
  181712. GABRIEL WEATHERHEAD
  181713. 12936
  181714. CHEM SOC REVCRVOLLHARDT DIELS ALDER INTRAMOLECULAR CYCLOADDITION REVIEW CYCLOBUTENE METAL TARGETM
  181715. 13945N
  181716. 2/28/96V~THERMAL, PHOTOCHEMICAL AND TRANSITION METAL MEDIATED ROUTES TO STEROIDS BY INTRAMOLECULAR DIELS ALDER REACTIONS OF O OXYLYLENEW
  181717. VOL 9   1980  PG 41a
  181718. GABRIEL WEATHERHEAD
  181719. 12937
  181720. B    SYNTHESISC`ALBINI PHOTOCYCLOADDITION SENSITIZATION PHYSICAL ORGANIC SENSITIZER TRIPLET CYCLOADDITION REVIEWM
  181721. 13946N
  181722. 2/28/96V'PHOTOSENSITIZATION IN ORGANIC SYNTHESISW
  181723. VOL 0   1981  PG 249a
  181724. GABRIEL WEATHERHEAD
  181725. 12938
  181726. ORGANIC PHOTOCHEMCDBALDWIN SYNTHESIS ALKENE ENONE TARGET PHOTOCYCLOADDITION REVIEW NAMEM
  181727. 13947N
  181728. 2/28/96V'SYNTHETIC ASPECTS OF [2+]CYCLOADDITIONSW
  181729. VOL 5   1981  PG 123a
  181730. GABRIEL WEATHERHEAD
  181731. 12939
  181732. ADV HETERO CHEMC8BLACK HETEROCYCLE BICYCLIC PHOTOCHEM NITROGEN AZA REVIEWM
  181733. 13948N
  181734. 2/28/96VXCHEMISTRY OF 1 AZA[3.1.0]BICYCLOHEXANES AND ANALOGS WITH FURTHER HETEROATOM SUBSTITUTIONW
  181735. VOL 27   1980  PG 1a
  181736. GABRIEL WEATHERHEAD
  181737. 12940
  181738. ACCT CHEM RESC:HECK CATALYST HALIDE ALKENE PALLADIUM HECK ADDITION REVIEWM
  181739. 13949N
  181740. 2/28/96V=PALLADIUM CATALYZED REACTIONS OF ORGANIC HALIDES WITH OLEFINSW
  181741. VOL 12   1979  PG 146a
  181742. GABRIEL WEATHERHEAD
  181743. 12941
  181744. ACCT CHEM RESCDREICH REAGENT ORGANOMETALLIC SELENIUM REVIEW ADDITION ALKENE ALCOHOLM
  181745. 13950N
  181746. 2/28/96V<FUNCTIONAL GROUP MANIPULATIONS USING ORGANOSELENIUM REAGENTSW
  181747. VOL 12   1979  PG 22a
  181748. GABRIEL WEATHERHEAD
  181749. 12942
  181750. HETEROCYCLIC COMPOUNDS SERIES
  181751. C8CHEESEMAN HETEROCYCLE PYRAZINE SYNTHESIS REACTION REVIEWM
  181752. 13951N
  181753. 2/28/96V&CONDENSED PYRAZINES   A OVERALL REVIEWW
  181754. VOL 35   1979  PG 0a
  181755. GABRIEL WEATHERHEAD
  181756. 12943
  181757. ADV HETERO CHEMCFECKSTEIN OXAZINE CYCLIZATION METHODOLOGY SYNTHESIS CONFORMATION REVIEWM
  181758. 13952N
  181759. 2/28/96V
  181760. 1,3 OXAZINE DERIVATIVESW
  181761. VOL 2   1978  PG 23a
  181762. GABRIEL WEATHERHEAD
  181763. 12944
  181764. ACCT CHEM RESCXDANISHEFSKY RING OPENING NUCLEOPHILE SYNTHESIS CYCLOPROPANE ELECTROPHILE ADDITION REVIEWM
  181765. 13953N
  181766. 2/28/96V0ELECTROPHILIC CYCLOPROPANES IN ORGANIC SYNTHESISW
  181767. VOL 12   1979  PG 66a
  181768. GABRIEL WEATHERHEAD
  181769. 12945
  181770. ANGEW CHEM INT ED ENGLCBBOTT DIAZONIUM SALT REACTIVE METHODOLOGY ALKENE PREPARATION REVIEWM
  181771. 13954N
  181772. 2/28/96VDALKENE DIAZONIUM SALTS: A NEW CHAPTER OF CLASSICAL ORGANIC CHEMISTRYW
  181773. VOL 18   1979  PG 259a
  181774. GABRIEL WEATHERHEAD
  181775. 12946
  181776. B    SYNTHESISC2LENZ ENAMIDE PHOTOREARRANGEMENT CYCLIZATION REVIEWM
  181777. 13955N
  181778. 2/28/96V
  181779. THE PHOTOCHEMISTRY OF ENAMIDESW
  181780. VOL 0   1978  PG 489
  181781. GABRIEL WEATHERHEAD
  181782. 12947
  181783. B    SYNTHESISC?REID CYCLOBUTENONE REACTION ENONE REVIEW FOUR RING DISPLACEMENTM
  181784. 13956N
  181785. 2/28/96VXTHE CHEMISTRY OF CYCLOBUTENDIONE: REACTIONS OF ALLYL , ALHENYL  AND ARYLCYCLOBUTENDIONESW
  181786. VOL 0   1978  PG 649a
  181787. GABRIEL WEATHERHEAD
  181788. 12948
  181789.     B    SYNTHESISCWOPPOLZER INTRAMOLECULAR CYCLOADDITION O QUINOMETHANE TARGET DIELS ALDER REACTIVE REVIEWM
  181790. 13957N
  181791. 2/28/96VTINTRAMOLECULAR CYCLOADDITION REACTIONS OF ORTHO QUINODIMETHANES IN ORGANIC SYNTHESISW
  181792. VOL 0   1978  PG 793a
  181793. GABRIEL WEATHERHEAD
  181794. 12949
  181795. ADV HETERO CHEMCJWENTRUP REVIEW NITRENE CARBENE INTRAMOLECULAR ADDITION INSERTION EXTRUSIONM
  181796. 13958N
  181797. 2/28/96VICARBENES AND NITRENES IN HETEROCYCLIC CHEMISTRY: INTRAMOLECULAR REACTIONSW
  181798. VOL 28   1981  PG 232a
  181799. GABRIEL WEATHERHEAD
  181800. 12950
  181801. B    SYNTHESISC=LAI MAGNESIUM GRIGNARD REVIEW EXPERIMENTAL ADDITION ACTIVATEDM
  181802. 13959N
  181803. 2/28/96V5GRIGNARD REAGENTS FROM CHEMICALLY ACTIVATED MAGNESIUMW
  181804. VOL 0   1981  PG 585
  181805. GABRIEL WEATHERHEAD
  181806. 12951
  181807. UNKNOWNCOBUNCEL ISOTOPE EFFECT KINETICS THEORY PHYSICAL ORGANIC ORGANIC DEUTERIUM REVIEWM
  181808. 13960N
  181809. 2/28/96V
  181810. ISOTOPES IN ORGANIC CHEMISTRYW
  181811. VOL 0   1975  PG 21a
  181812. GABRIEL WEATHERHEAD
  181813. 12952
  181814. CHIMIACBSEEBACH REVIEW NITRO METHODOLOGY UMPOLUNG SYNTHESIS ALKENE REAGENTM
  181815. 13961N
  181816. 2/28/96VDNITROALIPHATIC COMPOUNDS   IDEAL INTERMEDIATES IN ORGANIC SYNTHESIS?W
  181817. VOL 33   1979  PG 1a
  181818. GABRIEL WEATHERHEAD
  181819. 12953
  181820. B    SYNTHESISCCFISCHER REVIEW NITRO KETONE CARBANION ALKYLATION PREPARATION CYCLICM
  181821. 13962N
  181822. 2/28/96V6PREPARATION AND REACTIONS OF CYCLIC ALPHA NITROKETONESW
  181823. VOL 0   1980  PG 261a
  181824. GABRIEL WEATHERHEAD
  181825. 12954
  181826. JOCCACOREY NITRO ENONE KETONE REVIEW NITRATION PREPARATION METHODOLOGYM
  181827. 13963N
  181828. 2/28/96VtALPHA NITROKETONES. 3.STEREOCHEMISTRY OF THE NITRATION OF 1  ACETOXYCYCLOHEXENES: SYNTHESIS OF 2 NITROCYCLOHEXANONESW
  181829. VOL 46   1981  PG 3082a
  181830. GABRIEL WEATHERHEAD
  181831. 12955
  181832. TETRAHEDRON
  181833. CKWASSERMAN SINGLET OXYGEN SYNTHESIS ENE REACTION PEROXIDE REVIEW DIELS ALDERM
  181834. 13964N
  181835. 2/28/96V#SINGLET OXYGEN IN ORGANIC SYNTHESISW
  181836. VOL 37   YR[8]   PG 1825a
  181837. GABRIEL WEATHERHEAD
  181838. 12956
  181839. RUSS CHEM REVCGNOVIKOV NITRO ALKENE CYCLOADDITION DIENE DIELS ALDER PREPARATION REVIEWM
  181840. 13965N
  181841. 2/28/96V$DIENE SYNTHESIS WITH NITRO COMPOUNDSW
  181842. VOL 29   YR[60]   PG 2a
  181843. GABRIEL WEATHERHEAD
  181844. 12957
  181845. J CHEM SOC (B)COOLLIS ISOSYDNONE MESOIONIC DIPOLE DIPOLAR CYCLOADDITION AZOMETHINE IMINE REVIEWM
  181846. 13966N
  181847. 2/28/96V3ISOSYDNONES: SYNTHESIS AND REACTIONS [SEE REF CARD]W
  181848. VOL 0   YR[69]   PG 1185a
  181849. GABRIEL WEATHERHEAD
  181850. 12958
  181851. CHEM REVCXSTEWART SYDNONE REVIEW MESOIONIC CYCLOADDITION EXTRUSION AZOMETHINE IMINE CARBON DIOXIDEM
  181852. 13967N
  181853. 2/28/96V(THE CHEMISTRY OF SYDNONES [SEE REF CARD]W
  181854. VOL 64   YR[64]   PG 129a
  181855. GABRIEL WEATHERHEAD
  181856. 12959
  181857. ANGEW CHEM INT ED ENGLCJSAUER DIELS ALDER REVIEW THEORY REGIOCHEM MOLECULAR ORBITAL FMO STEREOCHEMM
  181858. 13968N
  181859. 2/28/96
  181860. V@MECHANISTIC ASPECTS OF DIELS ALDER REACTIONS: A CREITICAL SURVEYW
  181861. VOL 19   1980  PG 779a
  181862. GABRIEL WEATHERHEAD
  181863. 12960
  181864. CHEM REVCGHOUK REVIEW KETONE PHOTOCHEM ALKENE DI PI METHANE SPECTROSCOPY CARBONYLM
  181865. 13969N
  181866. 2/28/96VLTHE PHOTOCHEMISTRY AND SPECTROSCOPY OF BETA GAMMA UNSATURATED CARBONYL COMDSW
  181867. VOL 76   1976  PG 1a
  181868. GABRIEL WEATHERHEAD
  181869. 12961
  181870. HETEROCYCLESCJELNAGDI DIAZO DIPOLAR CYCLOADDITION HIGHER ORDER DIPOLE HETEROCYCLE REVIEWM
  181871. 13970N
  181872. 2/28/96V)CHEMISTRY OF HETEROCYCLIC DIAZO COMPOUNDSW
  181873. VOL 19   1982  PG 559a
  181874. GABRIEL WEATHERHEAD
  181875. 12962
  181876. JOCCMENONE PHOTOCYCLOADDITION INTRAMOLECULAR ALLENE REGIOCHEM TARGET REVIEW BECKERM
  181877. 13971N
  181878. 2/28/96VMINTRAMOLECULAR PHOTOADDITION OF TERMINAL ALLENES TO CONJUGATED CYCLOHEXENONESW
  181879. VOL 47   1982  PG 3297a
  181880. GABRIEL WEATHERHEAD
  181881. 12963
  181882. ANGEW CHEM INT ED ENGLCPHUISGEN REVIEW HIGHER ORDER CYCLIZATION DIPOLE DIPOLAR ELECTROCYCLIC HETEROCYCLEM
  181883. 13972N
  181884. 2/28/96
  181885. VOMECHANISTIC ASPECTS ASSOCIATED WITH THE 1,5 CYCLIZATION OF HIGHER ORDER DIPOLESW
  181886. VOL 19   1980  PG 947a
  181887. GABRIEL WEATHERHEAD
  181888. 12964
  181889. CHEM REVCJTAYLOR TURCHI HIGHER ORDER CYCLIZATION DIPOLE DIPOLAR ELECTROCYCLIC REVIEWM
  181890. 13973N
  181891. 2/28/96VF1,5 DIPOLAR CYCLIZATIONS AS A METHOD OF OBTAINING UNUSUAL HETEROCYCLESW
  181892. VOL 79   1979  PG 181a
  181893. GABRIEL WEATHERHEAD
  181894. 12965
  181895. TETRAHEDRONCMHEMETSBERGER ISOTOPE EFFECT DEUTERIUM PHOTOREARRANGEMENT DI PI METHANE REVIEWM
  181896. 13974N
  181897. 2/28/96VFPHOTOCHEM DEUTERIUM ISOTOPE EFFECT ON PHOTOREARRANGEMENT OF TRIPTYCENEW
  181898. VOL 38   1982  PG 1175a
  181899. GABRIEL WEATHERHEAD
  181900. 12966
  181901. UNKNOWNC9REVIEW AMIDE NITRO CARBANION DIPOLE STABILIZED ALKYLATIONM
  181902. 13975N
  181903. 2/28/96V<DIPOLE STABILIZED CARBANIONS. NOVEL AND USEFUL INTERMEDIATESW
  181904. VOL 0   YR[0]   PG 0a
  181905. GABRIEL WEATHERHEAD
  181906. 12967
  181907. ACCT CHEM RESCCSUZUKI BORON REVIEW ALKENE ALKYNE SYNTHESIS ORGANOMETALLIC ADDITIONM
  181908. 13976N
  181909. 2/28/96V(ORGANOBORATES IN NEW SYNTHETIC REACTIONS
  181910. VOL 15   1982  PG 178a
  181911. GABRIEL WEATHERHEAD
  181912. 12968
  181913. B    SYNTHESISCACHAN SILANE VINYL ALKYLATION METHODOLOGY REVIEW SYNTHESIS SILICONM
  181914. 13977N
  181915. 2/28/96V-ORGANOSILICONE COMPOUNDS IN ORGANIC SYNTHESISW
  181916. VOL 0   1979  PG 760a
  181917. GABRIEL WEATHERHEAD
  181918. 12969
  181919. CHEM SOC REVC6COLVIN SILICON SILANE VINYL METHODOLOGY REVIEW REAGENTM
  181920. 13978N
  181921. 2/28/96V
  181922. SILICONE IN ORGANIC SYNTHESISW
  181923. VOL 0   YR[65]   PG 15a
  181924. GABRIEL WEATHERHEAD
  181925. 12970
  181926. J SCIENT IND RESCXSUBRAHANYAM ISOXAZOLE METHODOLOGY REVIEW HETEROCYCLE CYCLOADDITION PREPARATION SYNTHESISM
  181927. 13979N
  181928. 2/28/96V$SYNTHETIC APPLICATIONS OF ISOXAZOLESW
  181929. VOL 33   1974  PG 304a
  181930. GABRIEL WEATHERHEAD
  181931. 12971
  181932. ACCT CHEM RESC:CHAN ALKENE SILICON EPOXIDE ALLENE ZWITTERION SILYL REVIEWM
  181933. 13980N
  181934. 2/28/96VQGENERATION AND CHEMISTRY OF ALLENE OXIDES. LEADING REFERENCES INCLUDED. SEE CARD.W
  181935. VOL 10   1977  PG 442a
  181936. GABRIEL WEATHERHEAD
  181937. 12972
  181938. ACCT CHEM RES
  181939. !CFOPPOLZER PHOTOCYCLOADDITION INTRAMOLECULAR 2+2 SYNTHESIS TARGET REVIEWM
  181940. 13981N
  181941. 2/28/96VYINTRAMOLECULAR 2+2 PHOTOADDITION. CYCLOBUTANE FRAGMENTATION SEQUENCE IN ORGANIC SYNTHESISW
  181942. VOL 15   1982  PG 135a
  181943. GABRIEL WEATHERHEAD
  181944. 12973
  181945. TETRAHEDRONC.REINECKE REVIEW BENZYNE HETARYNE ALKYNE STRAINM
  181946. 13982N
  181947. 2/28/96V    HETARYNESW
  181948. VOL 38   1982  PG 427a
  181949. GABRIEL WEATHERHEAD
  181950. 12974
  181951. TETRAHEDRONCBCHILDS SIGMATROPIC REARRANGEMENT ORBITAL SYMMETRY REVIEW CARBONIUMM
  181952. 13983N
  181953. 2/28/96V
  181954. CIRCUMABULATORY REARRANGEMENTSW
  181955. VOL 38   1982  PG 567a
  181956. GABRIEL WEATHERHEAD
  181957. 12975
  181958. PURE AND APPL CHEMC9SAKURAI ALKENE SILICON SILYL REVIEW CONDENSATION CARBONYLM
  181959. 13984N
  181960. 2/28/96V?REACTIONS OF ALLYLSILOANES AND APPLICATION TO ORGANIC SYNTHESISW
  181961. VOL 54   1982  PG 1a
  181962. GABRIEL WEATHERHEAD
  181963. 12976
  181964. CHEM SOC REVC=MOORE 2+2 KETENE CYCLOADDITION REVIEW CYANO CYANOKETENE AZIDEM
  181965. 13985N
  181966. 2/28/96V*CYANOKETENES: SYNTHESIS AND CYCLOADDITIONSW
  181967. VOL 3   1981  PG 289
  181968. GABRIEL WEATHERHEAD
  181969. 12977
  181970. &B    SYNTHESISC5SIMCHEN REVIEW SILICON SYNTHESIS TRIFLATE METHODOLOGYM
  181971. 13986N
  181972. 2/28/96VbTRIALKYLSILYL PERFLUOROALKANE SULFONATES AS SILYLATING AGENTS AND LEWIS ACIDS IN ORGANIC SYNTHESISW
  181973. VOL 0   1982  PG 1a
  181974. GABRIEL WEATHERHEAD
  181975. 12978
  181976. ANGEW CHEM INT ED ENGLC?CHRISTL BENZVALENE REVIEW CARBANION CARBENE NOVEL STRAINED RINGM
  181977. 13987N
  181978. 2/28/96V.BENZVALENE: PROPERTIES AND SYNTHETIC POTENTIALW
  181979. VOL 0   1981  PG 529a
  181980. GABRIEL WEATHERHEAD
  181981. 12979
  181982. ANGEW CHEM INT ED ENGLCBREETZ LEWIS ACID ALKYLATION ENOL SILICON REVIEW SYNTHESIS CATALYSTM
  181983. 13988N
  181984. 2/28/96V5LEWIS ACID INDUCED ALPHA ALKYLATION OF CARBONYL CMPDSW
  181985. VOL 21   1982  PG 96a
  181986. GABRIEL WEATHERHEAD
  181987. 12980
  181988. )B    SYNTHESISCTPETRZILKA DIPOLAR CYCLOADDITION CYCLOPENTADIENE REVIEW HETEROCYCLE DIENE DIELS ALDERM
  181989. 13989N
  181990. 2/28/96VAPREPN AND DIELS ALDER REACTIONS OF HETERO SUBSTITUTED 1,3  DIENESW
  181991. VOL 110   1981  PG 753a
  181992. GABRIEL WEATHERHEAD
  181993. 12981
  181994. ALDRICH CHIM ACTACFHASE UMPOLUNG METHODOLOGY REVIEW SYNTHESIS CARBANION ALKYLATION SULFURM
  181995. 13990N
  181996. 2/28/96V=A COMPOLATION OF REFERENCES ON FORMYL AND ACYL ANION SYNTHONSW
  181997. VOL 14   1981  PG 73a
  181998. GABRIEL WEATHERHEAD
  181999. 12982
  182000. HETEROCYCLESC:MUKERJEE HETEROCYCLE AZLACTONE REVIEW CARBANION ALKYLATIONM
  182001. 13991N
  182002. 2/28/96V/THE CHEMISTRY OF 4,5 DIHYDRO 5 OXO 1,3 OXAZOLESW
  182003. VOL 16   1981  PG 1995a
  182004. GABRIEL WEATHERHEAD
  182005. 12983
  182006. TETRAHEDRONC:SMITH REVIEW DIAZO KETONE ALKENE CYCLIZATION ACID CATALYSTM
  182007. 13992N
  182008. 2/28/96V,ACID PROMOTED DECOMPOSITION OF DIAZO KETONESW
  182009. VOL 37   1981  PG 2407a
  182010. GABRIEL WEATHERHEAD
  182011. 12984
  182012. TETRAHEDRONCJVIOLA PERICYCLIC ALKYNE SIGMATROPIC REARRANGEMENT CYCLIZATION REVIEW FLASHM
  182013. 13993N
  182014. 2/28/96V;INTRAMOLECULAR PERICYCLIC REACTIONS OF ACETYLENIC COMPOUNDSW
  182015. VOL 37   1981  PG 3765a
  182016. GABRIEL WEATHERHEAD
  182017. 12985
  182018. .B    SYNTHESISCMPINDER REVIEW SYNTHESIS REDUCTION HALIDE HYDROGENATION EXPERIMENTAL PALLADIUMM
  182019. 13994N
  182020. 2/28/96
  182021. .V%THE HYDROGENOLYSIS OF ORGANIC HALIDESW
  182022. VOL 6   1980  PG 425a
  182023. GABRIEL WEATHERHEAD
  182024. 12986
  182025. TETRAHEDRONCFCHAN EPOXIDE EPOXIDATION ALLENE FAVORSKI SILICON REVIEW CYCLOPROPANONEM
  182026. 13995N
  182027. 2/28/96V
  182028. CHEMISTRY OF ALLENE OXIDESW
  182029. VOL 36   1980  PG 2269a
  182030. GABRIEL WEATHERHEAD
  182031. 12987
  182032. CHEM SOC REVC.FLEMING SYNTHESIS REVIEW REAGENT METAL SILICONM
  182033. 13996N
  182034. 2/28/96V4SOME USES OF SILICONE COMPOUNDS IN ORGANIC SYNTHESISW
  182035. VOL 10   1981  PG 83a
  182036. GABRIEL WEATHERHEAD
  182037. 12988
  182038. 1B    SYNTHESISC>LAI EXPERIMENTAL METAL ORGANOMETALLIC REVIEW TECHNIQUE REAGENTM
  182039. 13997N
  182040. 2/28/96V5GRIGNARD REAGENTS FROM CHEMICALLY ACTIVATED MAGNESIUMW
  182041. VOL 8   YR[8]   PG 585a
  182042. GABRIEL WEATHERHEAD
  182043. 12989
  182044. CHEM SOC REVC<FOX PHOTOCHEM REVIEW CARBANION RADICAL ION ELECTRON TRANSFERM
  182045. 13998N
  182046. 2/28/96V(THE PHOTOEXITED STATES OF ORGANIC ANIONSW
  182047. VOL 0   1979  PG 253a
  182048. GABRIEL WEATHERHEAD
  182049. 12990
  182050. ANN SURV PHOTOCHEM
  182051. 3C>IMINE PHOTOCHEM ISOMERIZATION H ABSTRACTION CYCLIZATION REVIEWM
  182052. 13999N
  182053. 2/28/96V"CIS TRANS ISOMERIZATION OF IMMINESW
  182054. VOL 2   YR[0]   PG 101a
  182055. GABRIEL WEATHERHEAD
  182056. 12991
  182057. CHEM REVCFBEAK AMIDE CARBANION ORGANOMETALLIC ALKYLATION DIPOLE SYNTHESIS REVIEWM
  182058. 14000N
  182059. 2/28/96V
  182060. DIPOLE STABILIZED CARBANIONSW
  182061. VOL 28   1978  PG 275a
  182062. GABRIEL WEATHERHEAD
  182063. 12992
  182064. ANGEW CHEM INT ED ENGLCGOPPOLZER ENE REVIEW INTRAMOLECULAR SYNTHESIS THERMAL SIGMATROPIC TARGETM
  182065. 14001N
  182066. 2/28/96VkTHERMAL CYCLIZATION OF DIENES, ENYNES, ENONES & RELATED UNSAT. SYSTEMS. ENE REACTIONS IN ORGANIC SYNTHESIS.W
  182067. VOL 17   1978  PG 476a
  182068. GABRIEL WEATHERHEAD
  182069. 12993
  182070. JACSC6CALDWELL PHOTOCHEM REVIEW TEMPERATURE PHYSICAL ORGANICM
  182071. 14002N
  182072. 2/28/96V-TEMPARATURE EFFECTS IN ORGANIC PHOTOCHEMISTRYW
  182073. VOL 101   1979  PG 6960a
  182074. GABRIEL WEATHERHEAD
  182075. 12994
  182076. ANGEW CHEM INT ED ENGLC=SEEBACH REVIEW UMPOLUNG SYNTHESIS REAGENT METHODOLOGY SILICONM
  182077. 14003N
  182078. 2/28/96
  182079. 7V$USE OF SILICONE IN ORGANIC SYNTHESISW
  182080. VOL 18   1979  PG 239a
  182081. GABRIEL WEATHERHEAD
  182082. 12995
  182083. ANGEW CHEM INT ED ENGLCAQUINKERT REVIEW ASYMMETRIC CHIRAL INDUCTION RESOLUTION STEREOCHEMM
  182084. 14004N
  182085. 2/28/96VCSTEREOSELECTIVE SYNTHESIS OF ENANTIOMERICALLY PURE NATURAL PRODUCTSW
  182086. VOL 22   1983  PG 637a
  182087. GABRIEL WEATHERHEAD
  182088. 12996
  182089. CHEM REVCLFREEMAN WRITING DIHYDRO ISOXAZOLE HETEROCYCLE REARRANGEMENT REVIEW AZIRIDINEM
  182090. 14005N
  182091. 2/28/96V 2,3 DIHYDROISOXAZOLES   A REVIEWW
  182092. VOL 83   1983  PG 241a
  182093. GABRIEL WEATHERHEAD
  182094. 12997
  182095. CHEM REVCOLIEBMAN CYCLOPROPENE STRAIN REVIEW SMALL RING CYCLOPROPANE CYCLOBUTENE BICYCLICM
  182096. 14006N
  182097. 2/28/96V&A SURVEY OF STRAINED ORGANIC MOLECULESW
  182098. VOL 0   1976  PG 311a
  182099. GABRIEL WEATHERHEAD
  182100. 12998
  182101. CHEMISTRY IN BRITAINC3HAGEMAN FLASH THERMAL EXPERIMENTAL TECHNIQUE REVIEWM
  182102. 14007N
  182103. 2/28/96V"FLASH VACUUM THERMOLYSIS. A REVIEWW
  182104. VOL 9   1973  PG 206a
  182105. GABRIEL WEATHERHEAD
  182106. 12999
  182107. <B    SYNTHESIS
  182108. <CBRASMUSSEN ETHER REAGENT METHODOLOGY ALKYLATION SILICON REVIEW ENOLM
  182109. 14008N
  182110. 2/28/96VCO SILYLATED ENOLATES. VERSATILE INTERMEDIATES FOR ORGANIC SYNTHESISW
  182111. VOL 0   1977  PG 91a
  182112. GABRIEL WEATHERHEAD
  182113. 13000
  182114. =B SELECTIVE ORGANIC TRANSFORMATIONC&SINGER RADICAL STEREOCHEM VINYL REVIEWM
  182115. 14009N
  182116. 2/28/96V4STEREOCHEMICAL FEATURES OF VINYLIC RADICAL PROCESSESW
  182117. VOL 0   1970  PG 269a
  182118. GABRIEL WEATHERHEAD
  182119. 13001
  182120. ADV HETERO CHEMC8FOWLER REVIEW AZIRINE DIPOLE NITRILE YLIDE CYCLOADDITIONM
  182121. 14010N
  182122. 2/28/96V(A REVIEW DESCRIBING 2H AZIRINE CHEMISTRYW
  182123. VOL 13   1972  PG 45a
  182124. GABRIEL WEATHERHEAD
  182125. 13002
  182126. ANGEW CHEM INT ED ENGLC5GUNTHER SPECTROSCOPY NMR REVIEW COSY 2D INEPT WRITINGM
  182127. 14011N
  182128. 2/28/96VCMODERN PULSE METHODS IN HIGH RESOLUTION NMR SPECTROSCOPY (SEE CARD)W
  182129. VOL 22   1983  PG 350a
  182130. GABRIEL WEATHERHEAD
  182131. 13003
  182132. AUST J CHEMC5TAYLOR REVIEW SYNTHESIS DIKETONE WRITING EXPERIMENTALM
  182133. 14012N
  182134. 2/28/96V$SYNTHESIS OF 1,4 DIKETONES: A REVIEW
  182135. VOL 29   1976  PG 339a
  182136. GABRIEL WEATHERHEAD
  182137. 13004
  182138. AB    SYNTHESISC3SEEBACH UMPOLUNG SULFUR CARBANION ALKYLATION REVIEWM
  182139. 14013N
  182140. 2/28/96VPUMPOLUNG OF REACTIVITY OF CARBONYL COMPOUNDS THROUGH SULFUR  CONTAINING REAGENTSW
  182141. VOL 0   1976  PG 357a
  182142. GABRIEL WEATHERHEAD
  182143. 13005
  182144. BB    SYNTHESISCRRANGANATHAN CYCLOADDITION KETENE NAME DIELS ALDER SYNTHESIS CYCLOPENTADIENE REVIEWM
  182145. 14014N
  182146. 2/28/96V.KETENE EQUIVALENTS IN THE DIELS ALDER REACTIONW
  182147. VOL 0   1976  PG 289a
  182148. GABRIEL WEATHERHEAD
  182149. 13006
  182150. ARMSTRONG, A.
  182151. Tet. Lett.
  182152. A}STERIC CONTROL 
  182153. DIOXIRANES 
  182154. CARBAMATE 
  182155. LACTONES 
  182156. EPOXIDE 
  182157. EPOXIDATION 
  182158. PERACID
  182159. INTRAMOLECULAR
  182160. SYN SELECTIVITY BAEYER
  182161. VILLIGER
  182162. KETONE CARBONYL GROUPS ARE SHOWN TO DIRECT THE EPOXIDATION OF CYCLIC ALKENES WITH HIGHER SELECTIVITY THAN THAT DISPLAYED BY ESTERS. AN O
  182163. 18 LABELLING STUDY IS USED TO SHOW THAT A DIOXIRANE INTERMEDIATE IS NOT INVOLVED IN THESE REACTIONS.
  182164. 14015N
  182165. 2/28/96
  182166. A#KETONE
  182167. DIRECTED PERACID EPOXIDATION
  182168. 1994X    6155
  182169. 6158Y
  182170. 13007
  182171. MAKOSZA, M.
  182172. Tet. Lett.K
  182173. AROMATIC ALDEHYDES REACT WITH SULFONIUM SALTS OF CYCLIC AND CHAIN FORMALDEHYDE DITHIOACETALS IN PRESENCE OF AQUEOUS NAOH TO GIVE THE CORRESPONDING OXIRANES WHICH REARRANGE TO 2
  182174. THIOALKYLACETALDEHYDES.M
  182175. 14016N
  182176. 2/28/96
  182177. AQREACTION OF SULFONIUM SALTS OF FORMALDEHYDE DITHIOACETALS WITH AROMATIC ALDEHYDES
  182178. 1994 X    6141
  182179. 6142Y
  182180. 13008
  182181. DIXIT, A. N.
  182182. Tet. Lett.C
  182183. GLUTAMIC
  182184. ACID K
  182185. ALKOXYCARBONYL AND N
  182186. ARYLSULFONYL LACTAMS (1A 
  182187.  E) WERE PREPARED AND CONVERTED TO THE CORRESPONDING ACYCLIC PRODUCTS (2A 
  182188.  H) BY ACID CATALYZED CLEAVAGE OF THE LACTAM RING IN GOOD YIELDS AND EXCELLENT REGIOSELECTIVITY.M
  182189. 14017N
  182190. 2/28/96
  182191. A9FACILE ACID CATALYZED RING CLEAVAGE OF N
  182192. ACYLATED LACTAMS
  182193. 1994X    6133
  182194. 6134Y
  182195. 13009
  182196. SUZUKI, H.
  182197. Tet. Lett.C
  182198. BOND K
  182199. ADDITION OF CARBON NUCLEOPHILES TO CYCLIC N
  182200. ACYLIMINIUM SALTS CHIRALLY MODIFIED BY VARIOUS OPTICALLY ACTIVE PYRROLIDINES LEADS TO HIGHLY ENANTIOSELECTIVE SYNTHESIS OF 2
  182201. SUBSTITUTED PYRROLIDINES AND PIPERIDINES.M
  182202. 14018N
  182203. 2/28/96
  182204. ASYMMETRIC SYNTHESIS OF 2
  182205. SUBSTITUTED PYRROLIDINES AND PIPERIDINES BY NUCLEOPHILIC ADDITION TO N
  182206. ACYLIMINIUM IONS BEARING PYRROLIDINE CHIRAL AUXILIARIES
  182207. 1994 X    6119
  182208. 6122Y
  182209. 13010
  182210. CALLIER, A. C.
  182211. Tet. Lett.C
  182212. GROUP MIGRATION ACYL DEOXYGENATION ALCOHOLS CYANO 
  182213. NITROGEN CLEAVAGE 
  182214. AMIDYL RADICAL CYCLIZATION NITRILE ADDITION REARRANGEMENT K
  182215. BENZOYL HYDROXAMIC ACIDS REACT WITH TRIBUTYLSTANNANE IN THE PRESENCE OF AIBN TO GIVE AMIDYL OR CARBAMYL RADICALS WHICH CAN BE CAPTURED BY AN INTERNAL OLEFIN.M
  182216. 14019N
  182217. 2/28/96
  182218. AcAMIDYL AND CARBAMYL RADICALS BY STANNANE MEDIATED CLEAVAGE OF O
  182219. BENZOYL HYDROXAMIC ACID DERIVATIVES
  182220. 1994 X    6109
  182221. 6112Y
  182222. 13011
  182223. MASSACRET, M.
  182224. Tet. Lett.C
  182225. INTRAMOLECULAR ALKOXYPALLADATION CARBONYLATION PALLADIUM
  182226. CATALYZED HETEROANNULATION SUBSTITUTED ARYL HALIDES ALPHA
  182227. ADRENOCEPTOR ANTAGONISTS ABSOLUTE
  182228. CONFIGURATION GLYCEROL DERIVATIVES WB 4101 OXYPALLADATION RESOLUTION ENANTIOMERS K
  182229. VINYL
  182230. BENZODIOXANE WAS OBTAINED WITH E.E. UP TO 45 % BY CONDENSATION OF CATECHOL AND (Z)
  182231. BUTENE
  182232. DIYLBIS(METHYLCARBONATE) IN THE PRESENCE OF A CATALYTIC AMOUNT OF PALLADIUM(0) IN ASSOCIATION WITH CHIRAL LIGAND SUCH AS BINAP.M
  182233. 14020N
  182234. 2/28/96
  182235. A6ONE
  182236. POT PREPARATION OF CHIRAL 2
  182237. VINYL
  182238. BENZODIOXANE
  182239. 1994X    6093
  182240. 6096Y
  182241. 13012
  182242. A    COSSY, J.
  182243. Tet. Lett.C
  182244. SUBSTITUTED CYCLOALKANE
  182245. DIONE CYCLIC BETA
  182246. KETOESTER COPPER PERCHLORATE HEXAHYDRATE OXYGEN OXIDATIVE CLEAVAGE (OMEGA 1) OMEGA
  182247. DIOXOCARBOXYLIC ACIDS (OMEGA
  182248. OXOALKANEDIOIC ACIDS MONOESTERS DIOXYGEN CYCLOALKANONES 
  182249. .A PREPARATIVE METHOD FOR THE SYNTHESIS OF OMEGA
  182250. 1), OMEGA
  182251. DIOXOCARBOXYLIC ACIDS AND (OMEGA
  182252. OXOALKANEDIOIC ACIDS MONOESTERS BY RESPECTIVE OXIDATIVE CLEAVAGE OF 2
  182253. SUBSTITUTED CYCLOALKANE
  182254. DIONES AND CYCLIC BETA
  182255. KETOESTERS, BY COPPER PERCHLORATE IN ACETONITRILE IN AN OXYGEN ATMOSPHERE, IS REPORTED.
  182256. 14021N
  182257. 2/28/96
  182258. ArOXIDATIVE CLEAVAGE OF 2
  182259. SUBSTITUTED CYCLOALKANE
  182260. DIONES AND OF CYCLIC b
  182261. KETOESTERS BY COPPER PERCHLORATE/OXYGEN
  182262. 1994 X    6089
  182263. 6092Y
  182264. 13013
  182265. ADAM, W.
  182266. Tet. Lett.C
  182267. DIMETHYLDIOXIRANE SINGLET OXYGEN 2,3
  182268. DIMETHYLINDOLE 2,3
  182269. DIMETHYLBENZOFURANS 2,3
  182270. DIMETHYLIDENES DIOXETANES EPOXIDES QUINONE METHIDES PHOSPHOLANES DEOXYGENATION 
  182271. THE TRIPHENYLPHOSPHINE DEOXYGENATION OF 2,3
  182272. DIMETHYLLBENZOFURAN, 2,3
  182273. DIMETHYLINDOLE
  182274.  AND 2,3
  182275. DIMETHYLINDENE DIOXETANES 2 LEADS TO THE RESPECTIVE EPOXIDES 4 THROUGH THE INTERMEDIARY PHOSPHOLANES 3, OF WHICH THE INDENE AND INDOLE DERIVATIVES 3D,E WERE DETECTED BY LOW
  182276. TEMPERATURE NMR SPECTROSCOPY;  WITH EXCESS PH(3)P THE BENZOFURAN DIOXETANE 2N AFFORDS THE BENZOFURAN 1A, A NOVEL PROCESS IN WHICH THE RESULTING BENZOFURAN EPOXIDE 4A IS IN SITU DEOXYGENATED.
  182277. 14022N
  182278. 2/28/96
  182279. AvFACILE TRIPHENYLPHOSPHINE DEOXYGENATION OF BENZOFURAN DIOXETANES, THEIR EPOXIDES AND VALENCE
  182280. ISOMERIC QUINONE METHIDES
  182281. 1994 X    6063
  182282. 6066Y
  182283. 13014
  182284. BARTON, D. H. R.
  182285. Tet. Lett.C5DIATOMIC SULFUR GENERATION CHEMISTRY SULFENYL S
  182286. 2 S2 K
  182287. A NEW SYNTHESIS OF THIOLS IN HIGH YIELD UTILIZING CARBON RADICALS AND ELEMENTAL SULFUR IS DEMONSTRATED. THE PROCEDURE IS APP LICABLE TO 1 DEGREES, 2 DEGREES AND 3 DEGREES CARBOXYLIC ACIDS.M
  182288. 14023N
  182289. 2/28/96
  182290. AcTHE REACTION OF CARBON RADICALS WITH SULFUR. A CONVENIENT SYNTHESIS OF THIOLS FROM CARBOXYLIC ACIDS
  182291. 1994X    6057
  182292. 6060Y
  182293. 13015
  182294. TIMBERLAKE, J. W.
  182295. Tet. Lett.
  182296. DIMETHYLCYCLOPROPYL 4
  182297. METHYLPHENYL KETONE IN THE PRESENCE OF SML(2) AND DMPU IS A GOOD SET PROBE. THE ORTHO POSITIONS OF THE AROMATIC RING PROVIDE A GOOD SOURCE TO TRAP THE NEWLY FORMED TERTIARY RADICAL.M
  182298. 14024N
  182299. 2/28/96
  182300. A<2,2
  182301. DIMETHYLCYCLOPROPYL 4
  182302. METHYLPHENYL KETONE AS A SET PROBE
  182303. 1994 X    6043
  182304. 6046Y
  182305. 13016
  182306. A    COHEN, T.
  182307. Tet. Lett.CsCYCLOPROPANATIONS KETONES 
  182308. ENONES 
  182309. ACID 
  182310. COPPER HALIDE EQUIVALENT TRIFLATE 
  182311. LEWIS ACID THIOPHENOXIDE 
  182312. CHEAP REAGENTK
  182313. COMMERCIALLY AVAILABLE COPPER(I) BROMIDE 
  182314.  DIMETHYL SULFIDE COMPLEX IS COMPARABLE TO THE FAR MORE EXPENSIVE COPPER(I) TRIFLATE IN ASSISTING THE REMOVAL OF THE THIOPHENOXIDE GROUP FROM CERTAIN SUBSTRATES.M
  182315. 14025N
  182316. 2/28/96
  182317. AxCOPPER(I) BROMIDE
  182318. DIMETHYL SULFIDE COMPLEX 
  182319.  AN ALTERNATIVE TO COPPER(I) TRIFLATE FOR REMOVAL OF THE THIOPHENOXIDE GROUP
  182320. 1994 X    6041
  182321. 6042Y
  182322. 13017
  182323. GOH, J. B.
  182324. Tet. Lett.C.STEREOSELECTIVE SYNTHESIS CONDENSATIONS ACIDS 
  182325. ALDOL REACTIONS OF THE SODIUM ENOLATES OF ALPHA
  182326. DIBENZYLAMINO) ETHYL KETONES PROCEED IN A HIGHLY DIASTEREOSELECTIVE FASHION AND RESULT IN THE FORMATION OF THE ALL SYN ADDUCT. THE OBSERVED STEREOSELECTIVITIES ARE MOST EASILY UNDERSTOOD IN THE CONTEXT OF AN OPEN TRANSITION STATE.
  182327. 14026N
  182328. 2/28/96
  182329. A6ALDOL REACTIONS OF A
  182330. DIBENZYLAMINO) ETHYL KETONES
  182331. 1994X    6029
  182332. 6032Y
  182333. 13018
  182334. MAHADEVAN, A.
  182335. Tet. Lett.C
  182336. TRIFLUOROMETHYL SULFONES ORGANIC
  182337. SYNTHESIS 
  182338. TRIMETHYLSILYL SILICON TRIFLATE CARBANION VINYL IODIDE SULFONE LEAVING GROUP PETERSON OLEFIN ELIMINATIONK
  182339. A GENERAL ROUTE FOR THE SYNTHESIS OF METHYL TRIFLONE DERIVATIVES UTILIZING TRIFLIC ANHYDRIDE IS DESCRIBED. STEREOSELECTIVE SYNTHESIS OF E
  182340. VINYL AND DIENYL TRIFLONES HAS BEEN ACCOMPLISHED BY THE PETERSON OLEFINATION REACTION OF ALPHA
  182341. SILYL TRIFLONE ANIONS.M
  182342. 14027N
  182343. 2/28/96
  182344. AVA MILD AND CONVENIENT SYNTHESIS OF FUNCTIONALIZED METHYL TRIFLONES AND VINYL TRIFLONES
  182345. 1994 X    6025
  182346. 6028Y
  182347. 13019
  182348. STASZAK, M. A.
  182349. Tet. Lett.K
  182350. BIS(TERT
  182351. BUTOXYCARBONYL)
  182352. HYDROXYLAMINE HAS BEEN USED IN THE SYNTHESIS OF 5
  182353. LIPOXYGENASE INHIBITOR LY280810. IN ADDITION, THIS REAGENT HAS BEEN UTILIZED TO SYNTHESIZE A NUMBER OF OTHER HYDROXYLAMINE AND HYDROXAMIC ACID DERIVATIVES IN HIGH YIELDS.M
  182354. 14028N
  182355. 2/28/96
  182356. AoTHE USE OF N,O
  182357. BIS(TERT
  182358. BUTOXYCARBONYL)
  182359. HYDROXYLAMINE IN THE SYNTHESIS OF N
  182360. HYDROXYLAMINES AND HYDROXAMIC ACIDS
  182361. 1994X    6021
  182362. 6024Y
  182363. 13020
  182364. FITCH, R. W.
  182365. Tet. Lett.CjINHIBITORS PROTEASE ALCOHOLS 
  182366. ALUMINUM AMALGAM REDUCTION NITRO AMINO ALCOHOL ULTRASOUND EXPERIMENTAL AMINE
  182367. THE SONOCHEMICAL PROMOTED ALUMINUM AMALGAM REDUCTION OF 2
  182368. NITROALKANOLS PROVIDES AN IMPROVED YIELD AND ACCELERATED CONVERSION TO THE CORRESPONDING AMINO ALCOHOLS WHEN COMPARED TO THE NONULTRASOUND (BENCHTOP) REDUCTIONS. THE APP EARANCE OF BY
  182369. PRODUCT HYDROXYLAMINES IS MINIMIZED DURING THE ULTRASOUND PROMOTED REACTION. THE PRODUCT AMINO ALCOHOLS WERE CONVENIENTLY ACYLATED IN SITU WITH PROMOTION BY ULTRASOUND THUS AFFORDING THE N
  182370. ACYL DERIVATIVES IN THE SAME OPERATION.
  182371. 14029N
  182372. 2/28/96
  182373. AHTHE ALUMINUM AMALGAM REDUCTION OF 2
  182374. NITROALKANOLS PROMOTED BY ULTRASOUND
  182375. 1994X    6013
  182376. 6016Y
  182377. 13021
  182378. MARTIN, S. F.
  182379. Tet. Lett.C
  182380. CLOSING METATHESIS MANZAMINE
  182381. A DIENES 
  182382. HETEROCYCLE ALKALOID METATHESIS 2+2 METAL ORGANOMETALLIC MOLYBDENUM GRUBBS FISCHER CARBENE COMPLEX
  182383. A NOVEL TECHNIQUE FOR THE EFFICIENT SYNTHESIS OF FUSED NITROGEN HETEROCYCLES HAS BEEN DEVELOPED THAT FEATURES THE MOLYBDENUM ALKYLIDENE
  182384. CATALYZED METATHESIS OF ALPHA,OMEGA
  182385. DIENES CONTAINING A NITROGEN ATOM IN THE CHAIN LINKING THE TWO OLEFINIC FUNCTIONAL GROUPS. THE STARTING MATERIALS MAY BE READILY PREPARED IN THREE STEPS FROM SUCCINIMIDE AND GLUTARIMIDE VIA SEQUENTIAL MITSUNOBU ALKYLATION, SODIUM BOROHYDRIDE REDUCTION, AND ADDITION OF A VINYL CUPRATE TO AN N
  182386. ACYLIMINIUM SALT GENERATED INB
  182387.  SITU.
  182388. 14030N
  182389. 2/28/96
  182390. A?NOVEL ROUTE TO FUSED NITROGEN HETEROCYCLES BY OLEFIN METATHESIS
  182391. 1994X    6005
  182392. 6008Y
  182393. 13022
  182394. LINDERMAN, R. J.
  182395. Tet. Lett.CSELECTRON
  182396. TRANSFER OUTER
  182397. SPHERE INNER
  182398. SPHERE COMPLEXES FRAGMENTATION IRON(III) BOND KkTHE DIRECT OXIDATION OF (ALPHA
  182399. ALKOXYALKYL)TRIALKYLSTANNANES TO ESTERS BY REACTION WITH OZONE IS DESCRIBED.M
  182400. 14031N
  182401. 2/28/96
  182402. A]REGIOSELECTIVE OXIDATIVE CLEAVAGE OF FUNCTIONALIZED UNSYMMETRIC TETRAALKYLSTANNANES VIA OZONE
  182403. 1994X    5993
  182404. 5996Y
  182405. 13023
  182406. LANTOS, I.
  182407. Tet. Lett.C;MULTIHETERO
  182408. COPE REARRANGEMENT NITRONES ALPHA
  182409. AMIDO
  182410. KETONES
  182411. RCONDENSATION OF KETONE DERIVED NITRONES WITH N
  182412. METHYLCARBOXIMIDOYL CHLORIDE AFFORDS AFTER HYDROLYTIC WORKUP ALPHA
  182413. AMIDOKETONES. THE RESULTS ARE INTERPRETED IN TERMS OF THE FORMATION OF AN INTERMEDIATE CAPABLE OF UNDERGOING A FACILE [3,3] SIGMATROPIC REARRANGEMENT. ALDEHYDE DERIVED NITRONES FORM IMIDES VIA A [3+2] CYCLOADDITION REACTION.
  182414. 14032
  182415. 2/28/96
  182416. ARSYNTHESIS OF A
  182417. AMIDOKETONES. AN APPLICATION OF THE MULTI
  182418. HETERO COPE REARRANGEMENT
  182419. 1994 X    5977
  182420. 5980Y
  182421. 13024
  182422. RAMAN, J. V.
  182423. Tet. Lett.C*PLANE
  182424. NONSYMMETRIC CYCLOPENTADIENES ALDER 
  182425. AB INITIO CALCULATIONS REVEAL THAT THE INFLUENCE OF SPIROCONJUGATION ON THE HOMO OF 5
  182426. SUBSTITUTED CYCLOPENTADIENES IS WEAK RELATIVE TO ELECTRON WITHDRAWING EFFECTS AND THAT BOTH THE HOMO AND LUMO ENERGY LEVELS CAN BE LOWER THAN IN CYCLOPENTADIENE CONTRARY TO THE PREDICTIONS OF QUALITATIVE PERTURBATION THEORY. IN ACCORD WITH THESE THEORETICAL RESULTS, THE REACTION OF 5,5
  182427. DICYANOCYCLOPENTADIENE WITH CYCLOPENTADIENE YIELDS ONLY HETERODIMERS.
  182428. 14033N
  182429. 2/28/96
  182430. ON THE INFLUENCE OF SPIROCONJUGATION AND ELECTRON
  182431. WITHDRAWING EFFECTS ON THE FRONTIER ORBITAL ENERGIES OF 5
  182432. SUBSTITUTED CYCLOPENTADIENES
  182433. 1994 X    5973
  182434. 13025
  182435. IBARZO, J.
  182436. TetrahedronC
  182437. ETHERS METHYL 
  182438. DIBROMOETHANE HAS BEEN EMPLOYED AS AN EFFICIENT BROMINATING AGENT OF TERTIARY CARBANIONS IN STERICALLY CONGESTED MOLECULES, ALLOWING THE STEREOSELECTIVE SYNTHESIS OF 2
  182439. BROMOESTERS IN MILD CONDITIONS AND BEING COMPATIBLE WITH THE PRESENCE OF C
  182440. C DOUBLE BONDS. ALKYLATION IS THE PREDOMINATING PROCESS WHEN TERTIARY OR SECONDARY CARBANIONS IN FLEXIBLE OPEN CHAINS WERE USED. AN INTERPRETATION OF THESE FACTS IS PROVIDED.
  182441. 14034N
  182442. 2/28/96
  182443. AN1,2
  182444. DIBROMOETHANE IN THE SYNTHESIS OF 2
  182445. BROMOESTERS: BROMINATION VS ALKYLATION
  182446. 1994 X    9825
  182447. 9830Y
  182448. 13026
  182449. TANNER, D.
  182450. TetrahedronCjASYMMETRIC
  182451. SYNTHESIS TRANS
  182452. DISUBSTITUTED PYRROLIDINES ALDOL CONDENSATION LITHIUM ALKYLATION ALDEHYDES 
  182453. A SYSTEMATIC STUDY HAS BEEN MADE OF THE UTILITY OF READILY AVAILABLE C
  182454. SYMMETRIC AZIRIDINES AS AUXILIARIES FOR ASYMMETRIC ALKYLATION AND ALDOL REACTIONS OF AMIDE ENOLATES. AZIRIDINES WITH SUITABLY PLACED OXYGEN ATOMS IN THE SIDE CHAINS PROVED TO BE USEFUL FOR ALKYLATION REACTIONS (D.E. VALUES UP TO >98%) AND THE RESULTS ARE EXPLAINED IN TERMS OF AN INTRAMOLECULARLY CHELATED Z
  182455. ENOLATE SPECIES, WHICH COULD BE OBSERVED DIRECTLY BY MEANS OF NMR SPECTROSCOPY. IN CONTRAST, AZIRIDINE AUXILIARIEB6S LACKING SIDE
  182456. CHAIN OXYGENS PERFORMED BETTER IN ALDOL
  182457. 14035N
  182458. 2/28/96
  182459. A<ON THE USE OF C
  182460. SYMMETRIC AZIRIDINES AS CHIRAL AUXILIARIES
  182461. 1994 X    9797
  182462. 9824Y
  182463. 13027
  182464. TetrahedronCODIETHYL AZODICARBOXYLATE ESTERIFICATION REACTION TRIPHENYLPHOSPHINE INVOLVEMENT
  182465. oTHE MITSUNOBU AZIDE MODIFICATION HAS BEEN STUDIED BY NMR USING A HINDERED ALCOHOL AND THE PRINCIPLE INTERMEDIATES INVOLVED HAVE BEEN TENTATIVELY IDENTIFIED. THE ACCELERATED HYDROXYL GROUP ACTIVATION IN THE PRESENCE OF HYDRAZOIC ACID OR OF CATALYTIC QUANTITIES OF PHENOL GIVES US AN INSIGHT INTO THE REACTIVITY OF SOME OF THE INTERMEDIATES INVOLVED IN THESE REACTIONS.
  182466. 14036N
  182467. 2/28/96
  182468. AvTHE MECHANISM OF THE MITSUNOBU AZIDE MODIFICATION AND THE EFFECT OF ADDITIVES ON THE RATE OF HYDROXYL GROUP ACTIVATION
  182469. 1994X    9671
  182470. 9678Y
  182471. 13028
  182472. TOCHTERMANN, W.
  182473. DIELS
  182474. ALDER REACTION INTRAMOLECULAR ALDOL REACTION HYDROAZULENES LACTARANE SKELETON INJURED FRUIT BODIES SESQUITERPENE ALDEHYDES LARGE RINGS MUSHROOMS SCROBICULATUS SPECTROSCOPY M
  182475. 14037N
  182476. 2/28/96
  182477. ATSYNTHESIS OF FUNCTIONALIZED HYDROAZULENES 
  182478.  A NEW APPROACH TO THE LACTARANE SKELETON
  182479. 13029
  182480. BLECHERT, S.
  182481. TetrahedronC-STEREOSELECTIVE SYNTHESIS DERIVATIVES TAXANE 
  182482. -[2+2] PHOTOCYCLOADDITIONS BETWEEN ENONE 2 AND 2,3
  182483. DIHYDROPYRAN DERIVATIVES LEAD TO A NUMBER OF INTERESTING INTERMEDIATES 3A
  182484. E FOR TAXOID SYNTHESIS. FOLLOWING THIS STRATEGY THE STEREOSELECTIVE SYNTHESIS OF A BIOLOGICALLY ACTIVE TAXOID MIMICKING THE POLARITY OF THE CD RING PORTION IN TAXOL IS REPORTED.
  182485. 14038N
  182486. 2/28/96
  182487. SYNTHESIS OF NEW TAXOIDS
  182488. 1994X    9649
  182489. 9656Y
  182490. 13030
  182491. YANG, Y.
  182492. TetrahedronCvORGANOTIN REAGENTS OXIDATIVE ADDITION ORGANIC HALIDES PALLADIUM DERIVATIVES MECHANISMS KETONES COMPLEX LIGNANS CARBON 
  182493. FURAN NUCLEUS ABOUNDS IN NATURALLY OCCURRING OXYGEN
  182494. CONTAINING COMPOUNDS.(3) THEY ARE DIVIDED ACCORDING TO THEIR STRUCTURAL FEATURES INTO FURANOSESQUITERPENES, FURANOCEMBRANOLIDES AND FURANOID FATTY ACIDS, ETC. MANY OF THESE FURAN NATURAL PRODUCTS HAVE INTERESTING BIOLOGICAL ACTIVITIES, SUCH AS CYTOTOXIC AND ANTITUMOR PROPERTIES,(6,7) ANTISPASMODIC,(8) ANTIFEEDING,(9) AND SEVERAL OTHER POTENTIALLY USEFUL ACTIVITIES. MORE NATURAL FURAN
  182495. CONTAINING COMPOUNDS CONTINUE TO BE FOUND AT A RAPID PAB7CE.(10)  IN ADDITION TO BEING IMPORTANT BUILDING BLOCKS
  182496. 14039N
  182497. 2/28/96
  182498. REGIOSPECIFIC SYNTHESIS OF 3,4
  182499. DISUBSTITUTED FURANS .8. REGIOSPECIFIC SYNTHESIS OF 3,4
  182500. DISUBSTITUTED FURANS AND 3
  182501. SUBSTITUTED FURANS USING 3,4
  182502. BIS(TRI
  182503. BUTYLSTANNYL)FURAN AND 3
  182504. BUTYLSTANNYL)FURAN AS BUILDING BLOCKS
  182505. 1994X    9583
  182506. 9608Y
  182507. 13031
  182508. COLE, D. C.
  182509. TetrahedronM
  182510. 14040N
  182511. 2/28/96
  182512. A<RECENT STEREOSELECTIVE SYNTHETIC APPROACHES TO b
  182513. AMINO ACIDS
  182514. 1994X    9517
  182515. 9582Y
  182516. 13032
  182517. KABBARA, J.
  182518. SynlettC
  182519. CONJUGATE ALKYLATION TRIMETHYLALUMINIUM COPPER CATALYSIS UNSATURATED CARBONYL
  182520.  COMPOUNDS ORGANO
  182521. ALUMINUM REAGENTS ETHYLENIC ALDEHYDES ALPHA ME5CU3LI2 M
  182522. 14041N
  182523. 2/28/96
  182524. AVCOPPER
  182525. CATALYZED CONJUGATE ADDITION OF TRIMETHYLALUMINIUM TO A,b
  182526. UNSATURATED ALDEHYDES
  182527. 1994 X
  182528. 13033
  182529. HODGSON, D. M.
  182530. SynlettCICHROMIUM(III) BROMIDE ALDEHYDE METHYL KETONE REAGENTS REDUCTION CHLORIDE M
  182531. 14042N
  182532. 2/28/96
  182533. AZONE
  182534. STEP CHROMIUM(II)
  182535. MEDIATED HOMOLOGATION OF ALDEHYDES TO METHYL KETONES USING ME3SICBR3
  182536. 1994X
  182537. 13034
  182538. BOLM, C.
  182539. SynlettC
  182540. ALKYL ETHERS ACTIVE SECONDARY
  182541. AMINES ASYMMETRIC REDUCTION KETONES IMINES SULFOXIMINES HYDROGENATION COMPLEXES ALDEHYDES REAGENTS M
  182542. 14043N
  182543. 2/28/96
  182544. ACCATALYZED ENANTIOSELECTIVE BORANE REDUCTION OF KETIMINE DERIVATIVES
  182545. 1994X
  182546. 13035
  182547. MORENO, M. J. S. M.
  182548. SynlettC
  182549. SELECTIVE BROMINATION ALPHA,BETA
  182550. ENONES PHENYLTRIMETHYLAMMONIUM TRIBROMIDE ALPHA'
  182551. BROMO
  182552. ALPHA,BETA
  182553. ENONES TRIALKYSILYL DIENOL ETHERS SILYL ENOL ETHERSM
  182554. 14044N
  182555. 2/28/96
  182556. A=A NEW AND SELECTIVE A'
  182557. BROMINATION OF A,b
  182558. UNSATURATED KETONES
  182559. 1994 X
  182560. 13036
  182561. GUY, A.
  182562. SynlettCmLITHIUM PERCHLORATE CATALYSIS IMDA REACTION STEREOSELECTIVE CYCLOADDITION NITRO OLEFINS NITROALKENES OLEFINS M
  182563. 14045N
  182564. 2/28/96
  182565. AgCATALYSIS BY LITHIUM PERCHLORATE IN DIETHYL ETHER 
  182566.  INTRAMOLECULAR DIELS
  182567. ALDER REACTION OF NITROTRIENES
  182568. 1994X
  182569. 13037
  182570. RYU, I.
  182571. SynlettC~MACROCYCLIZATION FREE
  182572. RADICAL CARBONYLATION CARBON MONOXIDE 4
  182573. OXOLACTONE MACROLIDE ANTIBIOTICS CYCLIZATION LOPHOTOXIN LACTONESM
  182574. 14046N
  182575. 2/28/96
  182576. AGA N+1 STRATEGY FOR MACROCYCLIZATION BASED ON FREE
  182577. RADICAL CARBONYLATION
  182578. 1994X
  182579. 13038
  182580. LI, C.
  182581. Synlett
  182582. cC{BETA
  182583. AMINO ALCOHOL INTRAMOLECULAR CONJUGATE ADDITION VINYL SULFONE INTRAMOLECULAR NITROGEN ALKYLATION TRICHLOROACETIMIDATE M
  182584. 14047N
  182585. 2/28/96
  182586. INTRAMOLECULAR CONJUGATE ADDITION OF ALLYLIC TRICHLOROACETIMIDATES TO CYCLOALKENYL SULFONES 
  182587.  A REGIOSPECIFIC AND STEREOSELECTIVE SYNTHESIS OF AMINO ALCOHOL DERIVATIVES
  182588. 1994 X
  182589. 13039
  182590. SynlettCmIMINIUM SALTS TRIMETHYLSILANOLATE SODIUM SALT DEPROTONATION NON
  182591. AQUEOUS BASE ENAMINES SUBSTITUTION REACTIVITYM
  182592. 14048N
  182593. 2/28/96
  182594. AfSYNTHESIS OF A
  182595. ALKINYLENAMINES BY TRIMETHYLSILANOLATE
  182596. INDUCED A
  182597. DEPROTONATION OF PROPYNE IMINIUM SALTS
  182598. 1994X
  182599. 625-627Z
  182600. 13040
  182601. CRISTOFOLI, W. A.
  182602. PALLADIUM POLYENE CYCLIZATION FURANS HALENAQUINONE XESTOQUINONE SPONGE XESTOSPONGIA
  182603. SAPRA PROTEIN TYROSINE KINASE ANION CAPTURE PROCESSES DIELS
  182604. ALDER REACTION MARINE SPONGE M
  182605. 14049N
  182606. 2/28/96
  182607. A|PALLADIUM CATALYZED POLYENE CYCLIZATIONS 
  182608.  AN APPROACH TO THE PENTACYCLIC CARBON FRAMEWORK OF HALENAQUINONE AND XESTOQUINONE
  182609. 13041
  182610. TAMURA, O.
  182611. SynlettC
  182612. TRANSESTERIFICATION DIASTEREOSELECTIVE INTRAMOLECULAR CYCLOADDITION ALPHA
  182613. METHOXY CARBONYLNITRONE CHIRAL ALLYL ALCOHOLS 1,3
  182614. DIPOLAR CYCLOADDITION CYCLOADDITION NITRONES M
  182615. 14050N
  182616. 2/28/96
  182617. TANDEM TRANSESTERIFICATION AND DIASTEREOSELECTIVE INTRAMOLECULAR CYCLOADDITION OF A
  182618. METHOXYCARBONYLNITRONES WITH CHIRAL ACYCLIC ALLYL ALCOHOLS
  182619. 1994X
  182620. 13042
  182621. ARCHER, N. J.
  182622. SynlettC
  182623. THIIRANIUM SULFENYLATION ASYMMETRIC SULFONIUM DIMETHYL(METHYLTHIO)SULFONIUM FLUOROBORATE DMTSF PHENYLTHIO MIGRATION NUCLEOPHILIC
  182624. ATTACK EPISULFONIUM IONS OLEFINS TETRAHYDROFURANS M
  182625. 14051N
  182626. 2/28/96
  182627. SYNTHETIC ROUTES TO NOVEL HOMOCHIRAL SULFENYL SULFONIUM SALTS AND THEIR USE AS POTENTIAL ENANTIOSELECTIVE SULFENYLATING AGENTS 
  182628.  ASYMMETRIC SYNTHESIS VIA HOMOCHIRAL THIIRANIUM IONS
  182629. 1994 X
  182630. 13043
  182631. Doyle, M. P.B
  182632. SynlettC
  182633. HYDROFORMYLATION CATALYTIC DINUCLEAR RHODIUM(I) REGIOSELECTIVE MODIFIED RHODIUM CATALYSTS CRYSTAL
  182634. STRUCTURE REACTIVITY LIGANDS OLEFINS CLUSTER M
  182635. 14052N
  182636. 2/28/96
  182637. A]REGIOSELECTIVE HYDROFORMYLATION OF ALKENES CATALYZED BY DI(N
  182638. CARBOXYLATO)RHODIUM(I) COMPLEXES
  182639. 1994 X
  182640. 13044
  182641. TAMURA, E.
  182642. SynlettCGACTIVE (SALEN)MANGANESE(III) COMPLEXES CATALYTIC ASYMMETRIC EPOXIDATIONM
  182643. 14053N
  182644. 2/28/96
  182645. A`DIRECTING EFFECT OF 1,3
  182646. DIMETHYLIMIDAZOLIDINE IN ORTHO LITHIATION CHANGES WITH ITS VICINAL GROUP
  182647. 1994 X
  182648. 13045
  182649. NEMOTO, H.
  182650. SynlettC
  182651. HYDRINDAN PALLADIUM CATALYST ALKENIC CYCLOBUTANOL RING EXPANSION INSERTION ENANTIOSELECTIVE TOTAL SYNTHESIS (+)
  182652. LAURENE CONCISE M
  182653. 14054N
  182654. 2/28/96
  182655. A NOVEL ACCESS TO HYDRINDAN DERIVATIVES BY PALLADIUM MEDIATED TANDEM RING EXPANSION AND INSERTION REACTION OF ALKENIC CYCLOBUTANOLS
  182656. 1994X
  182657. 13046
  182658. TIEDEMANN, R.
  182659. SynlettCJOXIRANES ALLYL ANION DELTA
  182660. LACTONES ASYMMETRIC SYNTHESIS NATURAL
  182661. PRODUCTS M
  182662. 14055N
  182663. 2/28/96
  182664. METHOXY
  182665. PHENYLTHIO
  182666. PROPENE AS D1/D3 SYNTHON 
  182667.  APPlICATION FOR AN ASYMMETRIC SYNTHESIS OF (S)
  182668. PARASORBIC ACID
  182669. 1994X
  182670. 13047
  182671. NAKAMURA, T.
  182672. SynlettC
  182673. TAXOL ATROPISOMERISM 8
  182674. MEMBERED RING INTRAMOLECULAR CYCLIZATION CYCLIC BORONATE TAXANE CARBON FRAMEWORK RING CYCLIZATION NMR
  182675. SPECTROSCOPY M
  182676. 14056N
  182677. 2/28/96
  182678. A>SYNTHESIS OF THE TAXOL DERIVATIVES 
  182679.  CONTROL OF ATROPISOMERISM
  182680. 1994 X
  182681. 13048
  182682. BURGESS, K.
  182683. SynlettC
  182684. CYCLOPROPANE CYCLOPROPYLOG METHANOLOG CONSTRAINTS ENHANCED ANTIOPIATE ACTIVITY ALGA GRATELOUPIA
  182685. CARNOSA CYCLOPROPANE AMINO
  182686. ACIDS ALPHA
  182687. HYDROXY ESTERS 1
  182688. AMINO CYCLOPROPANECARBOXYLIC ACID 1
  182689. AMINOCYCLOPROPANE
  182690. CARBOXYLIC ACIDM
  182691. 14057N
  182692. 2/28/96
  182693. A.ASYMMETRIC SYNTHESES OF 2,3
  182694. METHANOAMINO ACIDS
  182695. 1994X
  182696. 13049
  182697. FARINA, V.
  182698. SynlettC
  182699. PALLADIUM CEPHALOSPORIN ALLENE CUPRATE STANNANE CROSS
  182700. COUPLING REACTIONS 3
  182701. SUBSTITUTED CEPHALOSPORINS PALLADIUM CATALYSIS ORGANOTIN REAGENTS CHEMISTRY
  182702. CEPHEM COUPLING TIN STANNANE PALLADIUM STILLE CROSS ALLENYL AZETIDINONE TRIFLATEM
  182703. 14058N
  182704. 2/28/96
  182705. ApTHE DEVELOPMENT OF ORGANOMETALLIC METHODOLOGIES FOR THE STEREOSPECIFIC INTRODUCTION OF CEPHALOSPORIN SIDE CHAINS
  182706. 1994 X
  182707. 13050
  182708. ZIPP, I.
  182709. Syn. Commun.CXPOTASSIUM HYDRIDE CONVENIENT METALATION KALIATION REDUCTION REAGENT ACIDS ROUTE LIH NAH M
  182710. 14059N
  182711. 2/28/96
  182712. A_LITHIUM HYDRIDE AND LITHIUM TRIMETHOXYBOROHYDRIDE 
  182713.  A COMPARATIVE STUDY OF THEIR REDUCING POWER
  182714. 1994X    2515
  182715. 2523Y
  182716. 13051
  182717. MEHTA, P. G.
  182718. Syn. Commun.M
  182719. 14060N
  182720. 2/28/96
  182721. A(A NOVEL SYNTHESIS OF SQUARIC ACID ESTERS
  182722. 1994X    2497
  182723. 2502Y
  182724. 13052
  182725. A    SHANG, X.
  182726. Syn. Commun.C
  182727. EFFICIENT ADDITION BETA M
  182728. 14061N
  182729. 2/28/96
  182730. A=CERIUM(III) AMIDE ENOLATE 
  182731.  ADDITION TO ALDEHYDES AND KETONES
  182732. qX    2485
  182733. 2489Y
  182734. 13053
  182735. BUSZEK, K. R.
  182736. Syn. Commun.C
  182737. NEOCARZINOSTATIN CHROMOPHORE
  182738. A MEDIATED ALDOL REACTION (Z)
  182739. DIENEDIYNE SYSTEMS ANALOGS CORE (E)
  182740. DIENEDIYNE DIENEDIYNES ALDEHYDES ENEDIYNES M
  182741. 14062N
  182742. 2/28/96
  182743. SYNTHESIS OF A 9
  182744. MEMBERED RING VIA THE INTRAMOLECULAR NI(II)/CR(II)
  182745. MEDIATED COUPLING REACTION 
  182746.  UNUSUAL EFFECT OF CONCENTRATION ON THE COURSE OF THE REACTION
  182747. 1994X    2461
  182748. 2472Y
  182749. 13054
  182750. ANGELES, E.
  182751. Syn. Commun.C
  182752. REDUCTIVE CARBONYLATION AZIDES M
  182753. 14063N
  182754. 2/28/96
  182755. A/A SIMPLE METHOD FOR THE SYNTHESIS OF CARBAMATES
  182756. 1994X    2441
  182757. 2447Y
  182758. 13055
  182759. BAO, W. L.
  182760. Syn. Commun.C
  182761. ORGANIC
  182762. SYNTHESIS M
  182763. 14064N
  182764. 2/28/96
  182765. APSMI2
  182766. INDUCED ASYMMETRIC REDUCTION OF BENZIL IN THE PRESENCE OF CHIRAL SURFACTANT
  182767. 1994X    2437
  182768. 2440Y
  182769. 13056
  182770. ZHU, R. S.
  182771. Syn. Commun.M
  182772. 14065N
  182773. 2/28/96
  182774. AJSTUDY ON THE 'DRY REACTION' WITHOUT ANY MEDIUM UNDER MICROWAVE IRRADIATION
  182775. 1994X    2417
  182776. 2421Y
  182777. 13057
  182778. KOYANAGI, J.
  182779. J. Het. Chem.M
  182780. 14066N
  182781. 2/28/96
  182782. A>PREPARATION OF 3
  182783. BROMO
  182784. METHYLFURAN AND 4
  182785. BROMO
  182786. METHYLFURAN
  182787. 1994X    1093
  182788. 1095Y
  182789. 13058
  182790. SARD, H.
  182791. J. Het. Chem.C
  182792. HETEROAROMATIC RING
  182793. SYSTEMS M
  182794. 14067N
  182795. 2/28/96
  182796. AwAN UNEXPECTED PRODUCT DURING SYNTHESIS OF 3
  182797. PHENYLISOQUINOLINE 
  182798.  IMPROVED PREPARATION OF 4
  182799. HYDROXY
  182800. PHENYLISOQUINOLINE
  182801. 1994 X    1085
  182802. 1087Y
  182803. 13059
  182804. PINDUR, U.
  182805. J. Het. Chem.C}DIELS
  182806. ALDER REACTIONS ANNELLATED INDOLE ACCESS VINYLINDOLES ALKALOIDS CARBODIENOPHILES 2
  182807. VINYLINDOLES DERIVATIVES TRANSITION M
  182808. 14068N
  182809. 2/28/96
  182810. AMCARBAZOLE SYNTHESIS VIA AN IN SITU TRAPPING STRATEGY WITH INDOLYL ENOL ETHERS
  182811. 1994X
  182812. 13060
  182813. COCCO, M. T.
  182814. J. Het. Chem.M
  182815. 14069N
  182816. 2/28/96
  182817. AVSYNTHESIS OF 2H
  182818. PYRAZOLO[3,4
  182819. B]PYRIDIN
  182820. OLES VIA CYCLIZATION OF PYRAZOLACRYLONITRILES
  182821. 1994X
  182822. 13061
  182823. KATRITZKY, A. R.
  182824. J. Het. Chem.M
  182825. 14070N
  182826. 2/28/96
  182827. A[MANNICH REACTIONS OF CARBONYL COMPOUNDS AND ENAMINES WITH BENZOTRIAZOLE AS THE Nu COMPONENT
  182828. 1994X
  182829. 13062
  182830. Wang, X. H.B
  182831. J. Het. Chem.CnORGANIC
  182832. SYNTHESIS DNA CLEAVAGE NEOCARZINOSTATIN VINYLALLENES CARBONATES OXIDATION SULFONES SYSTEMS ROUTE ACID M
  182833. 14071N
  182834. 2/28/96
  182835. A-DIELS
  182836. ALDER REACTIVITY OF VINYLSULFOXYALLENES
  182837. 1994X
  182838. 13063
  182839. COUTTS, I. G. C.
  182840. J. Het. Chem.C
  182841. IMIDAZOLES M
  182842. 14072N
  182843. 2/28/96
  182844. AcREMARKABLE SELECTIVITY IN THE REACTION OF 1
  182845. TRITYL
  182846. LITHIOIMIDAZOLES WITH T
  182847. BUTYL HALOGENOACETATES
  182848. 1994X
  182849. 13064
  182850. CARLSEN, H. J.
  182851. J. Het. Chem.C
  182852. REARRANGEMENT M
  182853. 14073N
  182854. 2/28/96
  182855. A;SYNTHESIS OF UNSYMMETRICALLY SUBSTITUTED 4H
  182856. 1,2,4
  182857. TRIAZOLES
  182858. 1994X
  182859. 13065
  182860. SCHNEIDER, R.
  182861. J. Het. Chem.C}FUNCTIONALIZED CYCLIC ETHERS BETA
  182862. HYDROXY CARBONYLS RELATIVE STEREOCHEMISTRY ROUTE DELTA
  182863. ISOXAZOLINES ISOXAZOLES ADDITIONS M
  182864. 14074N
  182865. 2/28/96
  182866. DISUBSTITUTED FURO[3,4
  182867. C]ISOXAZOLES AND 7,7
  182868. DISUBSTITUTED PYRANO
  182869. C]ISOXAZOLES FROM INTRAMOLECULAR CYCLOADDITION REACTIONS
  182870. 1994X
  182871. 13066
  182872. KATRITZKY, A. R.
  182873. J. Het. Chem.C
  182874. BENZOTRIAZOLE DERIVATIVES M
  182875. 14075N
  182876. 2/28/96
  182877. A3NEW ROUTES TO SELECTIVELY METHYLATED BENZIMIDAZOLES
  182878. 1994X
  182879. 13067
  182880. KATRITZKY, A. R.
  182881. J. Het. Chem.C9SYNTHETIC AUXILIARY SALTS HETEROCYCLES REACTIVITY ETHERS M
  182882. 14076N
  182883. 2/28/96
  182884. AqCHEMISTRY OF A
  182885. (BENZOTRIAZOL
  182886. YL)ALKYLPYRIDINES 
  182887.  UNUSUAL NUCLEOPHILIC ATTACK AT C
  182888. 3A OF THE BENZOTRIAZOLYL RING
  182889. 1994 X
  182890. 13068
  182891. BOSSIO, R.
  182892. J. Het. Chem.C
  182893. DERIVATIVES M
  182894. 14077N
  182895. 2/28/96
  182896. A[STUDIES ON ISOCYANIDES AND RELATED COMPOUNDS 
  182897.  AN UNUSUAL SYNTHESIS OF IMIDAZOLYLOXAZOLONES
  182898. 1994X
  182899. 13069
  182900. NYIONDIBONGUEN, E.
  182901. J.C.S. Perkin Trans. 1M
  182902. 14078N
  182903. 2/28/96
  182904. Ad[4+2]
  182905. CYCLOADDITIONS OF 3
  182906. AMINO
  182907. IMINO
  182908. THIENO[3,4
  182909. C][1]BENZOPYRAN WITH SOME SELECTED DIENOPHILES
  182910. 1994X    2191
  182911. 2195Z
  182912. 13070
  182913. LAUTENS, M.
  182914. J.C.S. Perkin Trans. 1
  182915. CONORBORNADIENES HEXACHLOROCYCLOPENTADIENE DELTACYCLENES ADDITIONS OLEFINS RINGS M
  182916. 14079N
  182917. 2/28/96
  182918. AwSTEREOSELECTIVITY IN THE HOMO
  182919. DIELS
  182920. ALDER REACTION: EFFECT OF A REMOTE 7
  182921. SUBSTITUENT ON NICKEL
  182922. CATALYSED CYCLOADDITIONS
  182923. 1994X    2143
  182924. 2150Z
  182925. 13071
  182926. A    HONDA, T.
  182927. J.C.S. Perkin Trans. 1C
  182928. ALPHA
  182929. MANNOSIDASE INHIBITOR QUINOLIZIDINE ALKALOIDS SWAINSONA
  182930. CANESCENS KINETIC RESOLUTION ORGANIC
  182931. SYNTHESIS ACID REARRANGEMENT REDUCTION OXIDATION PRODUCTS M
  182932. 14080N
  182933. 2/28/96
  182934. AvENANTIOSELECTIVE SYNTHESIS OF INDOLIZIDINE ALKALOIDS: FORMAL SYNTHESIS OF (
  182935. SWAINSONINE AND OF (+)
  182936. PUMILIOTOXIN 251D
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  182948. NITROPROPANES REACTIVITY ALKYLATION M
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  182951. ALKENYL A
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  182983. FACIAL STEREOSELECTIVITIES IN DIELS
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  183119. MONOSUBSTITUTED 2
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  183374. AdEXPERIMENTS DIRECTED TOWARDS THE SYNTHESIS OF ANTHRACYCLINONES .22. NOVEL CYCLOPROPANATION REACTIONS
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  183376. 1577Y
  183377. 13108
  183378. HAQUE, M. R.
  183379. Aust. J. Chem.CQNUCLEOPHILIC
  183380. SUBSTITUTION SELECTIVITY PRINCIPLE TRANSITION
  183381. STATE MECHANISM MODEL M
  183382. 14117N
  183383. 2/28/96
  183384. AcAMBIDENT HETEROCYCLIC REACTIVITY 
  183385.  ALKYLATION OF 4
  183386. SUBSTITUTED AND 2,4
  183387. DISUBSTITUTED BENZIMIDAZOLES
  183388. 1994X    1523
  183389. 1535Y
  183390. 13109
  183391. A    ALLER, E.
  183392. Tet. Lett.CNCATALYTIC REACTIONS ORGANIC
  183393. SYNTHESIS YLIDE FORMATION CYCLOPROPANATION ESTERS 
  183394. RHODIUM(II) ACETATE CATALYSED DECOMPOSITION OF THE PHENYLDIAZOACETATES 3 IN THE PRESENCE OF ALCOHOLS (METHANOL, PROPAN
  183395. OL, TERT
  183396. BUTANOL) LED TO THE O
  183397. II INSERTION PRODUCTS 4
  183398. 6 IN VARYING YIELDS;  THE DIASTERCOMERIC EXCESS OF THE PRODUCT RANGED FROM 5
  183399. 14118N
  183400. 2/28/96
  183401. DIASTEREOSELECTIVITY IN THE O
  183402. H INSERTION REACTIONS OF RHODIUM CARBENOIDS DERIVED FROM PHENYLDIAZOACETATES OF HOMOCHIRAL ALCOHOLS
  183403. 1994 X    5949
  183404. 5952Y
  183405. 13110
  183406. MAJUMDAR, K. C.
  183407. Tet. Lett.C@CLAISEN REARRANGEMENT DEMETHYLSUBEROSIN DERIVATIVES CYCLIZATION K
  183408. CYCLOPENTENYL)
  183409. HYDROXY[1]BENZOPYRAN
  183410. ONE(2) OR ITS ACETATE (3) REACTS WITH PYRIDINE HYDROTRIBROMIDE TO GIVE THE FUSED FURO CHROMONE (4) IN 90% YIELD, WHICH ON REFLUXING IN 50% H2SO4 FURNISHES THE FUSED FURO COUMARIN (5) IN 87% YIELD.M
  183411. 14119N
  183412. 2/28/96
  183413. ABAN UNUSUAL CHROMONE FORMATION, AND ITS REARRANGEMENT TO A COUMARIN
  183414. 1994 X    5927
  183415. 5930Y
  183416. 13111
  183417. CATELLANI, M.
  183418. Tet. Lett.C8COUMARINS PALLADIUM CATALYSIS CARBON MONOXIDE COMPLEXES 
  183419. PALLADIUM(0) HAS BEEN FOUND TO CATALYSE THE REACTION OF AN AROMATIC CARBON
  183420. IODIDE BOND WITH CARBON MONOXIDE, THE TRIPLE BOND OF ALKYNES AND THE ALLYLIC CARBON OF AN ORTHO ALKENOIC CHAIN TO FORM A 3,4
  183421. DISUBSTITUTED COUMARIN RING IN SATISFACTORY YIELD UNDER MILD CONDITIONS.
  183422. 14120N
  183423. 2/28/96
  183424. A NEW PALLADIUM
  183425. CATALYZED SYNTHESIS OF 3,4
  183426. DISUBSTITUTED COUMARINS FROM 3
  183427. ALKENOATES OF ORTHO
  183428. IODOPHENOL, PHENYLACETYLENE AND CARBON MONOXIDE
  183429. 1994X    5923
  183430. 5926Y
  183431. 13112
  183432. CATELLANI, M.
  183433. Tet. Lett.
  183434. COUMARIN PALLADIUM CATALYSIS CYCLIZATION OXIDATIVE
  183435. ADDITION PROMOTED CYCLIZATION INSERTION REACTIONS MECHANISM CHLORIDE PATHWAYS HALIDES K
  183436. A NEW PALLADIUM
  183437. CATALYZED SYNTHESIS OF 4
  183438. ALKYLCOUMARINS IS REPORTED, BASED ON INTRAMOLECULAR ARYLATION OF THE 3
  183439. ALKENOIC CHAIN OF AN ORTHO
  183440. IODOPHENYL ESTER.M
  183441. 14121N
  183442. 2/28/96
  183443. ApINTRAMOLECULAR CYCLIZATION OF ORTHO
  183444. IODOPHENYL 3
  183445. BUTENOATE TO 4
  183446. METHYLCOUMARIN: CATALYSIS BY PALLADIUM COMPLEXES
  183447. 1994X    5919
  183448. 5922Y
  183449. 13113
  183450. SOUTO, A. A.
  183451. Tet. Lett.CcTRANS
  183452. PARINARIC ACID POLYENE FATTY
  183453. ACIDS FLUORESCENT
  183454. PROBES STEREOCHEMISTRY HETEROGENEITY MEMBRANE 
  183455. AN EASY AND PRACTICAL SYNTHESIS OF ALL(E)
  183456. 2,4,6,8,10
  183457. DODECAPENTAENOIC ACID (1), ALL(E)
  183458. 5,7,9,11,13
  183459. PENTADECAPENTAENOIC ACID (2), ALL(E)
  183460. 8,10,12,14,16
  183461. OCTA DECAPENTAENOIC ACID (3) AND ITS (8Z)
  183462. ISOMER (4) BY APP LICATION OF THE WITTIG OLEFINATION REACTION IS DESCRIBED.
  183463. 14122N
  183464. 2/28/96
  183465. AGA GENERAL AND PRACTICAL SYNTHESIS OF LINEAR CONJUGATED PENTAENOIC ACIDS
  183466. 1994X    5907
  183467. 5910Y
  183468. 13114
  183469. LAWRENCE, N. J.
  183470. Tet. Lett.C
  183471. WITTIG REACTIONS YLIDES RING 
  183472. ALKENES MAY BE SYNTHESISED FROM (ALPHA
  183473. BROMOBENZYL)BENZYLDIPHENYLPHOSPHONIUM SALTS BY THE ACTION OF AMINE BASES. A SERIES OF STILBENES WAS SYNTHESISED BY THE ACTION OF N
  183474. BROMOSUCCINIMIDE AND 2,2,6,6
  183475. TETRAMETHYLPIPERIDINE DIRECTLY UPON DIBENZYLDIPHENYL PHOSPHONIUM SALTS. THE REACTION, ESSENTIALLY A PHOSPHONIUM ANALOGUE OF THE RAMBERG BACKLUND DISPLAYS A SIMILAR LEVEL OF CIS SELECTIVITY AS THAT SHOWN BY THE PARENT SULFONE.
  183476. 14123N
  183477. 2/28/96
  183478. A4RAMBERG
  183479. BACKLUND TYPE REACTIONS OF PHOSPHONIUM SALTS
  183480. 1994 X    5903
  183481. 5906Y
  183482. 13115
  183483. MATSUSHITA, K.
  183484. Tet. Lett.C"CARBONATES ALLENYL HALIDES ESTERS 
  183485. %TERTIARY PROPARGYLIC ALCOHOLS REACTED WITH CARBON MONOXIDE IN THE PRESENCE OF CATALYTIC QUANTITIES OF A CATIONIC PALLADIUM(II) COMPLEX, [PD(CH3CN)(2)(PP H(3))(2)](BF4)(2), TO AFFORD 2(5H)
  183486. FURANONES AND/OR 2,3
  183487. DIENOIC ACIDS, THE PRECURSOR OF THE FURANONES, IN GOOD YIELDS UNDER MILD CONDITIONS.
  183488. 14124N
  183489. 2/28/96
  183490. AzCARBONYLATION OF TERTIARY PROPARGYLIC ALCOHOLS CATALYZED BY A CATIONIC PALLADIUM(II) COMPLEX: SYNTHESIS OF 2(5H)
  183491. FURANONES
  183492. 1994 X    5889
  183493. 5890Y
  183494. 13116
  183495. SHIMAMOTO, T.
  183496. Tet. Lett.C
  183497. ACIDS 
  183498. THE PHENYLTHIO GROUP OF 4
  183499. PHENYLTHIOAZETIDINONE (1) WAS READILY SUBSTITUTED WITH COPP ER(I) SALTS OF CARBOXYLATES, THIOCARBOXYLATES, AND COPPER(I) ENOLATES OF MALONATES AND BETA
  183500. KETOESTERS TO GIVE SYNTHETIC INTERMEDIATES (3 AND 4) FOR PENEM AND CARBAPENEM ANTIBIOTICS.
  183501. 14125N
  183502. 2/28/96
  183503. AbCOPPER
  183504. ASSISTED SUBSTITUTION REACTION FOR PHENYLTHIO GROUP OF A 4
  183505. PHENYLTHIOAZETIDINONE DERIVATIVE
  183506. 1994 X    5887
  183507. 5888Y
  183508. 13117
  183509. MARINETTI, A.
  183510. Tet. Lett.C2ASYMMETRIC HYDROSILYLATION MOP CATALYST COMPLEXES 
  183511. %HYDROSILYLATIONS OF STYRENE AND CYCLOPENTADIENE ARE PERFORMED IN THE PRESENCE OF PHOSPHETANE
  183512. PALLADIUM 1:1 AND 2:1 COMPLEXES. AN UNPRECEDENTED INHIBITORY EFFECT OF THE SECOND : PHOSPHINE LIGAND SUGGESTS A MONOPHOSPHINE
  183513. PD CATALYZED PROCESS WHICH PROCEEDS THROUGH FOUR
  183514. COORDINATE INTERMEDIATES.
  183515. 14126N
  183516. 2/28/96
  183517. AFAN INVESTIGATION INTO A PALLADIUM CATALYZED HYDROSILYLATION OF OLEFINS
  183518. 1994X    5861
  183519. 5864Y
  183520. 13118
  183521. PERALEZ, E.
  183522. Tet. Lett.CHSURFACE NATURE ELECTRON
  183523. TRANSFER MECHANISM MAGNESIUM REACTIVITY BROMIDE 
  183524. ;INHIBITORS, IN VERY LOW CONCENTRATION, INHIBIT THE REACTION BETWEEN 1
  183525. BROMO
  183526. METHYL
  183527.  BUTANE AND MAGNESIUM OBTAINED BY VAPORIZATION OF METAL. FOR SUCH A MAGNESIUM DERIVATIVE, THE INHIBITORS CANNOT PLAY THE ROLE OF ''KILLERS'' FOR ACTIVE SITES. A CHAIN REACTION FOR THE FORMATION OF THE GRIGNARD REAGENT IS PROPOSED.
  183528. 14127N
  183529. 2/28/96
  183530. A9NEW PERSPECTIVES IN THE FORMATION OF THE GRIGNARD REAGENT
  183531. 1994 X    5857
  183532. 5860Y
  183533. 13119
  183534. SCHINZER, D.
  183535. Tet. Lett.C$INTRAMOLECULAR ADDITION BUTENOLIDES 
  183536. PROPARGYLIC SILANES OF TYPE 2,4,9,11, AND 13 UNDERGO SMOOTH CYCLIZATION IN REFLUXING BENZENE AND IN THE PRESENCE OF AIBN AND TRIBUTYLTIN HYDRIDE. RING CLOSURE OF CARBOCYCLES AND ALSO OF 5
  183537.  AND 6
  183538. MEMBERED 0
  183539. HETEROCYCLIC SINGS IS ACHIEVED IN HIGH CHEMICAL YIELDS.
  183540. 14128N
  183541. 2/28/96
  183542. AdSYNTHESIS OF CARBO
  183543.  AND HETEROCYCLIC COMPOUNDS BY RADICAL
  183544. INITIATED CYCLIZATIONS OF PROPARGYLSILANES
  183545. 1994 X    5853
  183546. 5856Y
  183547. 13120
  183548. Bach, T.B
  183549. Tet. Lett.C/PATERNO
  183550. BUCHI REACTION PHOTOCHEMICAL
  183551. REACTIONS 
  183552. .THE PHOTOCYCLOADDITION OF UNSYMMETRICALLY SUBSTITUTED ALKENES TO AN ALDEHYDE LEADS TO EIGHT POSSIBLE ISOMERIC OXETANES. IN SHARP CONTRAST TO MOST OTHER SUBSTRATES, SILYL
  183553. ENOL ETHERS 1 WHICH BEAR A VINYLIC BETA
  183554. SUBSTITUENT FAVOR ONLY A SINGLE STEREO
  183555.  AND REGIOISOMER 2 AS MAJOR PRODUCT OF THIS REACTION.
  183556. 14129N
  183557. 2/28/96
  183558. STEREOSELECTIVE PHOTOCYCLOADDITION OF SILYL ENOL ETHERS TO ALDEHYDES. CONFIGURATIONAL CONTROL OF THREE STEREOGENIC CENTERS In OXETANES
  183559. 1994 X    5845
  183560. 5848Y
  183561. 13121
  183562. BURKE, S. D.
  183563. Tet. Lett.M
  183564. 14130N
  183565. 2/28/96
  183566. AIA SHORT ROUTE TO AVENACIOLIDE AND ISOAVENACIOLIDE VIA RADICAL CYCLIZATION
  183567. 1994X    5841
  183568. 5844Y
  183569. 13122
  183570. BURKE, S. D.
  183571. Tet. Lett.
  183572. SUBSTITUTED TETRAHYDROFURANS CAPTODATIVE STABILIZATION RADICAL CYCLIZATION ANIONIC CYCLIZATION RING
  183573. CLOSURE ORGANIC
  183574. SYNTHESIS ATOM TRANSFER FORCE
  183575. FIELD ACETYLENES ROUTES 
  183576. HYDROFURAN METHOD ANTIBIOTIC IONOPHORE THIO TRANSITION STATE RADICAL DIASTEREOSELECTIVITY TARGET
  183577. CYCLIZATION OF THE RADICALS DERIVED FROM CS BOND HOMOLYSIS AS WELL AS VIA 1,5
  183578. HYDROGEN ATOM TRANSFER AFFORDED TETRAHYDROFURANS IN HIGH YIELD. AN ALTERNATIVE ANIONIC CYCLIZATION METHOD PROVIDED THE ANTI DIASTEREOMER PREFERENTIALLY.M
  183579. 14131N
  183580. 2/28/96
  183581. AO2,3
  183582. DISUBSTITUTED TETRAHYDROFURAN SYNTHESIS VIA RADICAL AND ANIONIC CYCLIZATION
  183583. 1994 X    5837
  183584. 5840Y
  183585. 13123
  183586. PEI, Y. H.
  183587. Tet. Lett.C
  183588. CHEMICAL DIVERSITY SOLID
  183589. PHASE SYNTHESIS [3+2] CYCLOADDITION NITRILE OXIDES ISOXAZOLE ISOXAZOLINE DERIVATIVES ACID 
  183590. SOLID PHASE ISOXAZOLE ISOXAZOLINE PHARMACOPHORE DIPOLAR
  183591. CYCLOADDITION REGIOCHEM RESIN REGIOCHEMISTRYK
  183592. A SERIES OF ISOXAZOLES AND ISOXAZOLINES WERE SYNTHESIZED ON SOLID
  183593. PHASE THROUGH [3+2] CYCLOADDITION REACTIONS OF ALKYNES AND ALKENES WITH HIGHLY REACTIVE NITRILE OXIDES.M
  183594. 14132N
  183595. 2/28/96
  183596. A{POST
  183597. MODIFICATION OF PEPTOID SIDE CHAINS: [3+2] CYCLOADDITION OF NITRILE OXIDES WITH ALKENES AND ALKYNES ON THE SOLID
  183598. PHASE
  183599. 1994X    5825
  183600. 13124
  183601. TROST, B. M.
  183602. Tet. Lett.C
  183603. LIGANDS SUBSTITUTION COMPLEXES K
  183604. THE SOURCE OF THE ASYMMETRIC INDUCTION USING CHIRAL LIGANDS COMPRISING BIS(2
  183605. DIPHENYL PHOSPHINOENZOYL) DERIVATIVES OF CHIRAL DIAMINES AND DIOLS IN PALLADIUM(0) CATALYZED ALLYLIC ALKYLATIONS IS PROBED.M
  183606. 14133N
  183607. 2/28/96
  183608. AUON THE NATURE OF THE ASYMMETRIC INDUCTION IN A PALLADIUM CATALYZED ALLYLIC ALKYLATION
  183609. 1994X    5817
  183610. 5820Y
  183611. 13125
  183612. HAN, G. H.
  183613. WEINREB
  183614. Tet. Lett.
  183615. ANISOMYCIN NITROGEN ALPHA 
  183616. DIAZONIUM RADICAL HYDROGEN ATOM TRANSFER OXIDATION IMINIUM ION METHOD ALKOXY AMIDE OXIDATION ISATOIC ANHYDRIDE ORTHO AMINO BENZAMIDEK
  183617. DIAZOTIZATION OF O
  183618. AMINOBENZAMIDES IN METHANOL IN THE PRESENCE OF A CATALYTIC AMOUNT OF CUCL AFFORDS ALPHA
  183619. METHOXYBENZAMIDES IN GOOD YIELDS.M
  183620. 14134N
  183621. 2/28/96
  183622. A1A CONVENIENT SYNTHETIC METHOD FOR AMIDE OXIDATION
  183623. 1994 X    5813
  183624. 5816Y
  183625. 13126
  183626. GLASS, R. S.
  183627. Tet. Lett.C/ENANTIOSELECTIVE OXIDATIONS SULFIDES CHEMISTRY 
  183628. OXIDATION OF SUBSTITUTED THIETANES 1A, B, AND 6 WITH M
  183629. CHLOROPEROXYBENROIC ACID PREFERENTIALLY GIVES THE CORRESPONDING CIS
  183630. SULFOXIDES WITH MODEST DIASTEREOSELECTIVITY. SELECTIVE OXIDATION OF THE TRANS OVER THE CIS DIASTEREOMERIC PAIRS OF SULFOXIDES 2A, 3A;  2B, 3B;  7, 8 OCCURS WITH MODERATE SELECTIVITY WITH M
  183631. CHLOROPEROXYBENZOIC ACID. THE BASIS FOR THESE SELECTIVITIES IS HYDROGEN BONDING BETWEEN THE 3
  183632. SUBSTITUENT AND THE PERACID.
  183633. 14135N
  183634. 2/28/96
  183635. AgDIASTEREOSELECTIVE OXIDATION OF SUBSTITUTED THIETANES AND STEREOSELECTIVE OXIDATION OF THEIR SULFOXIDES
  183636. 1994X    5809
  183637. 5812Y
  183638. 13127
  183639. PUTS, R. D.
  183640. Tet. Lett.C
  183641. OXAZOLINES UTILITY ACIDS 
  183642. ;THE SYNTHESIS, MECHANISM OF FORMATION AND PURIFICATION OF NEW OXAZOLINES CONTAINING BINAPHTHYL AND BIPHENYL MOIETIES BASED ON ALKYLATION OF 2
  183643. METHYL
  183644. OXAZOLINE WITH ALKYL HALIDES ARE DESCRIBED. YIELDS UP TO 87% HAVE BEEN REALIZED, AND THE METHOD IS APP LICABLE TO THE SYNTHESES OF OTHER 2
  183645. SUBSTITUTED
  183646. OXAZOLINES.
  183647. 14136N
  183648. 2/28/96
  183649. AXFACILE ALKYLATION OF 2
  183650. METHYL
  183651. OXAZOLINE: SYNTHESIS OF NOVEL 2
  183652. SUBSTITUTED
  183653. OXAZOLINES
  183654. 1994 X    5779
  183655. 5782Y
  183656. 13128
  183657. ORNSTEIN, P. L.
  183658. Tet. Lett.
  183659. WE REPORT THE PREPARATION OF A HYDROISOQUINOLINE INTERMEDIATE POTENTIALLY USEFUL FOR THE SYNTHESIS OF SOME EXCITATORY AMINO ACID ANTAGONISTS. THE REQUISITE STEREOCHEMISTRY IS ESTABLISHED BY AN INTRAMOLECULAR DIELS
  183660. ALDER REACTION, AND THE ABSOLUTE STEREOCHEMISTRY IS ULTIMATELY DERIVED FROM S ASPARTIC ACID. ALSO REPORTED IS AN EFFICIENT SYNTHESIS OF METHYL N
  183661. CBZ ASPARTATE BETA
  183662. ALDEHYDE.
  183663. 14137N
  183664. 2/28/96
  183665. INTRAMOLECULAR DIELS
  183666. ALDER ROUTE TO 6
  183667. OXODECAHYDROISOQUINOLINE
  183668. CARBOXYLATE INTERMEDIATES FOR THE SYNTHESIS OF CONFORMATIONALLY CONSTRAINED EXCITATORY AMINO ACID ANTAGONISTS
  183669. 1994 X    5759
  183670. 5762Y
  183671. 13129
  183672. BALDWIN, J. E.
  183673. TetrahedronK
  183674. SAMARIUM (II) IODIDE
  183675. MEDIATED RING CLOSURES, OF SUBSTITUTED N
  183676. PROPARGYL SUBSTRATES DERIVED FROM L
  183677. SERINE, HAVE BEEN USED TO GENERATE A SERIES OF 2,3,4
  183678. TRISUBSTITUTED PYRROLIDINE DERIVATIVES.M
  183679. 14138N
  183680. 2/28/96
  183681. A[THE SYNTHESIS OF SUBSTITUTED PYRROLIDINES BY A SAMARIUM(II) IODIDE MEDIATED RING CLOSURE .2
  183682. 1994X    9425
  183683. 9438Y
  183684. 13130
  183685. BALDWIN, J. E.
  183686. TetrahedronC1ORGANIC
  183687. SYNTHESIS CYCLIZATION DIIODIDE REDUCTION K
  183688. SAMARIUM (II) IODIDE
  183689. MEDIATED RING CLOSURES, OF SUBSTITUTED N
  183690. ALLYL DERIVATIVES OF L
  183691. SERINE, HAVE BEEN USED TO GENERATE A SERIES OF 2,3,4
  183692. TRISUBSTITUTED PYRROLIDINE DERIVATIVES.M
  183693. 14139N
  183694. 2/28/96
  183695. A[THE SYNTHESIS OF SUBSTITUTED PYRROLIDINES BY A SAMARIUM(II) IODIDE
  183696. MEDIATED RING CLOSURE .1
  183697. 1994X    9411
  183698. 9424Y
  183699. 13131
  183700. HUNTER, R.
  183701. TetrahedronC
  183702. SILYL ENOL ETHERS MASKED MICHAEL REACTION ETHYLTHIOKETENE DITHIOACETALS THIONIUM IONS EQUIVALENTS NUCLEOPHILES ANNULATION ALDEHYDES ELECTRON CARBON 
  183703. PUMMERER
  183704. DERIVED SUBSTITUTED VINYLTHIONIUM IONS (ALLYL PHENYL SULFOXIDE, TMSOFF, ETN(I
  183705. PR)(2), CH2CL2, 
  183706. 78 DEGREES C) WITH A BETA
  183707. TRIMETHYLSILYLMETHYL (2), GAMMA
  183708. PHENYL (14), OR GAMMA
  183709. PHENYLTHIO (15) GROUP ALLYLATE THE ENOL SILYL ETHERS OF ACETOPHENONE (3) AND CYCLOHEXANONE (4) IN GOOD YIELD. ALLYLATION WITH (14) AND (15) REQUIRED SLOW ADDITION OF BASE IN ORDER TO LIMIT THE RATE OF PRODUCTION OF INTERMEDIATE, AND THUS AVOID UNWANTED SILA
  183710. PUMMERER TYPE PRODUCTS. HUNIG'S BASE CONJUGATE ADDITB;ION WAS NOT OBSERVED IN THESE CASES. BOTH THE (E)
  183711.  AND (Z)
  183712. 14140N
  183713. 2/28/96
  183714. AAALLYLATION WITH PUMMERER
  183715. GENERATED SUBSTITUTED VINYLTHIONIUM IONS
  183716. 1994X    9365
  183717. 9376Y
  183718. 13132
  183719. BUENO, A. B.
  183720. TetrahedronCYASYMMETRIC
  183721. SYNTHESIS CONFORMATIONAL
  183722. ANALYSIS ORGANIC
  183723. COMPOUNDS STEREOCHEMISTRY MACROLIDE 
  183724. THE HIGHLY STEREOSELECTIVE HYDRIDE REDUCTIONS OF CHIRAL 2
  183725. TOLYLSULFINYL
  183726. CYCLOPENTANONES AND CYCLOHEPTANONES ARE DESCRIBED. WITH DIBAL (ELECTROPHILIC HYDRIDE) THE CONFIGURATION INDUCED AT C
  183727. 1 IS CONTROLLED BY THE SULFINYL GROUP (1,3
  183728. ASYMMETRIC INDUCTION), AND IT CAN BE INVERTED BY USING ZNCL2 AS CATALYST. WITH L
  183729. SELECTRIDE THE STEREOSELECTIVITY IS DIRECTED BY THE C
  183730. 2 CHIRAL GROUPS (1,2
  183731. ASYMMETRIC INDUCTION). OTHER NUCLEOPHILIC HYDRIDES GAVE RESULTS WHICH DEPEND ON THE REAGENTS AND THE SIZB
  183732. E OF THE RINGS.
  183733. 14141N
  183734. 2/28/96
  183735. ALSTEREOSELECTIVE HYDRIDE REDUCTIONS OF CHIRAL 2
  183736. TOLYLSULFINYLCYCLOALKANONES
  183737. 1994X    9355
  183738. 9364Y
  183739. 13133
  183740. NAZARENO, M. A.
  183741. Tetrahedron
  183742. S(RN)1 HALOCYCLOPROPANE ELECTRON TRANSFER STEREOSELECTIVITY CARBANIONS SRN1 MECHANISM NUCLEOPHILIC
  183743. SUBSTITUTION STEREOCHEMISTRY DERIVATIVES RADICALS DMSO 
  183744. THE PHOTOSTIMULATED REACTION OF 7
  183745. IODOBICYCLO[4.1.0]
  183746. HEPTANE (7
  183747. IODONORCARANE, 1, A MIXTURE OF CA. 1:1 OF THE EXO:ENDO ISOMERS) WITH ACETOPHENONE ENOLATE ION 2 IN DMSO AT 60 DEGREES C GAVE THE SUBSTITUTION PRODUCTS 3A (EXO) AND 3B (ENDO) IN 87% YIELD (WITH AN EXO:ENDO RATIO OF 16). IN THE DARK AT 60 DEGREES C, NOT ONLY THE IPSO SUBSTITUTION PRODUCTS 3A AND 3B (51%), BUT ALSO THE CINE SUBSTITUTION PRODUCT 4 WERE FORMED (20%) BY AN ELIMINATION
  183748. ADDITION REACTION. IN THE DARK AND AT ROOM TEMPEBARATURE THERE IS NO REACTION. IT IS SUGGESTED THAT 1 REACTS WITH 2
  183749. 14142N
  183750. 2/28/96
  183751. SRN1 REACTIONS OF 7
  183752. IODOBICYCLO[4.1.0]HEPTANE WITH CARBANIONS. A NOVEL STEREOSELECTIVE C
  183753. C BOND FORMATION ON CYCLOPROPANE RINGS
  183754. 1994 X    9267
  183755. 9274Y
  183756. 13134
  183757. CAINELLI, G.
  183758. B    SynthesisCeBETA
  183759. LACTAMS  3,4
  183760. DIHYDROPYRIDIN
  183761. ONES POTASSIUM T
  183762. BUTOXIDE IMINES ESTER
  183763. ENOLATES TAXOL SILYLIMINES M
  183764. 14143N
  183765. 2/28/96
  183766. ArESTER
  183767. IMINE CONDENSATION MEDIATED BY POTASSIUM TERT
  183768. BUTOXIDE: SYNTHESIS OF b
  183769. LACTAMS AND 3,4
  183770. DIHYDROPYRIDIN
  183771. 1994 X
  183772. 13135
  183773. ROCHET, P.
  183774. B    Synthesis
  183775. ENANTIOPURE ALKOXYALLENES OR PROPARGYL ETHERS CHIRAL AUXILIARIES METHYLENE
  183776. GAMMA
  183777.  BUTYROLACTONES DIASTEREOSELECTIVE ADDITIONS ALPHA
  183778. METHYLENE ALKOXYALLENES ALDEHYDES METHOXYALLENE DERIVATIVES REAGENTS M
  183779. 14144N
  183780. 2/28/96
  183781. AUAN EFFICIENT SYNTHESIS OF ENANTIOPURE 1
  183782. ALKOXY
  183783. PROPADIENES FROM PROPARGYL BROMIDE
  183784. 1994 X
  183785. 13136
  183786. SCHANK, K.
  183787. B    SynthesisCCCOPPER(II) ACETYLACETONATE/MONOACYLOXYLATION BY PEROXYDICARBONATES M
  183788. 14145N
  183789. 2/28/96
  183790. INTRODUCTION OF OXYGEN FUNCTIONS INTO THE A
  183791. POSITION OF b
  183792. DIKETONES .8. ACYLOXYLATION OF COPPER(II) ACETYLACETONATE WITH DIACYL PEROXIDES
  183793. 1994X
  183794. 13137
  183795. AHLBRECHT, H.
  183796. B    SynthesisC
  183797. AXIALLY DISSYMMETRIC MOLECULES ALUMINUM
  183798. HYDRIDE REAGENTS ENANTIOSELECTIVE REDUCTION ASYMMETRIC
  183799. SYNTHESIS STANNYLATION ALDEHYDES KETONES M
  183800. 14146N
  183801. 2/28/96
  183802. AxREDUCTION OF IMIDOYLSTANNANES: A SIMPLE METHOD FOR THE PREPARATION OF A
  183803. STANNYLAMINES CONTAINING A SECONDARY AMINO GROUP
  183804. 1994X
  183805. 13138
  183806. BOSSIO, R.
  183807. B    SynthesisCUISOCYANIDES CYANOACETIC ACID ARYLGLYOXAL ANILS UGI REACTION PYRROLES NOVEL SYNTHESIS M
  183808. 14147N
  183809. 2/28/96
  183810. A\STUDIES ON ISOCYANIDES AND RELATED COMPOUNDS: A NOVEL SYNTHESIS OF PYRROLES VIA UGI REACTION
  183811. 1994 X
  183812. 13139
  183813. LERIVEREND, C.
  183814. B    SynthesisC
  183815. ORGANOSULFUR CHEMISTRY SILICON M
  183816. 14148N
  183817. 2/28/96
  183818. A^A NEW MILD SYNTHESIS OF UNSYMMETRICAL DISULFIDES BY REACTION OF DITHIOPEROXYESTERS WITH THIOLS
  183819. 1994 X
  183820. 13140
  183821. LUBINEAU, A.
  183822. B    Synthesis
  183823. WATER HYDROPHOBIC EFFECTS AQUEOUS MEDIA REACTIVITY IN WATER DIELS
  183824. ALDER REACTION SILYL ENOL ETHERS CHIRAL SULFONATED PHOSPHINES PALLADIUM
  183825. CATALYZED HYDROGENATIONS OPENING METATHESIS POLYMERIZATION UNSATURATED CARBONYL
  183826. COMPOUNDS M
  183827. 14149N
  183828. 2/28/96
  183829. A WATER
  183830. PROMOTED ORGANIC REACTIONS
  183831. 1994X
  183832. 13141
  183833. FRENZEL, A.
  183834. J. Organomet. Chem.C
  183835. SILYL LITHIUM SILANE M
  183836. 14150N
  183837. 2/28/96
  183838. AISYNTHESIS OF 1,2
  183839. BIS(SILYL) INDOLENE IN ANIONIC 1,2
  183840. SILYL GROUP MIGRATION
  183841. 1994X
  183842. 13142
  183843. HODGSON, D. M.
  183844. J. Organomet. Chem.
  183845. 14151N
  183846. 2/28/96
  183847. A;CHROMIUM(II)
  183848. BASED METHODS FOR CARBON CARBON bOND FORMATION
  183849. 1994 X
  183850. 13143
  183851. CRISTAU, H. J.
  183852. J. Organomet. Chem.CYPHOSPHONATE STEREOSELECTIVE SYNTHESIS CUPRATE ADDITION PHOSPHORUS VINYLPHOSPHONATES ACID M
  183853. 14152N
  183854. 2/28/96
  183855. AOA CONVENIENT STEREOSELECTIVE SYNTHESIS OF DISUBSTITUTED ALK
  183856. ENYL PHOSPHONATES
  183857. 1994X
  183858. 13144
  183859. DAVIES, A. G.
  183860. J. Organomet. Chem.C;TIN HYDRIDE FREE RADICALS HYDROSTANNATION HYDROSTANNOLYSIS M
  183861. 14153N
  183862. 2/28/96
  183863. A.THE FORMATION OF DISTANNANES FROM TIN HYDRIDES
  183864. 1994X
  183865. 13145
  183866. Hwu, C. C.B
  183867. J. Organomet. Chem.C
  183868. CHROMIUM MOLYBDENUM CARBENE SMALL RING NUCLEAR MAGNETIC RESONANCE INFRARED SPECTROSCOPY MASS SPECTROMETRY METAL CARBENE COMPLEXES ALPHA,BETA
  183869. UNSATURATED DOUBLE
  183870. BOND DIELS
  183871. ALDER REACTIONS M
  183872. 14154N
  183873. 2/28/96
  183874. AwREGIOSELECTIVE FORMATION OF ALLYLIDENECYCLOPROPANES FROM FISCHER CHROMIUM CARBENE COMPLEXES AND VINYLIDENECYCLOPROPANES
  183875. 1994 X
  183876. 13146
  183877. CAMBIE, R. C.
  183878. J. Organomet. Chem.C
  183879. PODOCARPIC ACID LITHIUM COPPER BENZANNULATION RADICAL RING EXPANSION TERTIARY BENZAMIDES ORTHO LITHIATION ORTHO
  183880. METALATION COMPLEXES AROMATIZATION M
  183881. 14155N
  183882. 2/28/96
  183883. AsBENZANNULATION OF PODOCARPIC ACID DERIVATIVES VIA DIRECTED ORTHO METALLATION AND LITHIUM
  183884. COPPER(I) TRANSMETALLATION
  183885. 1994 X
  183886. 13147
  183887. MARCOCONTELLES, J.
  183888. (VOL 59, PG 1234, 1994)M
  183889. 14156N
  183890. 2/28/96
  183891. DIG FREE
  183892. RADICAL CARBOCYCLIZATIONS: A NEW STRATEGY FOR THE SYNTHESIS OF CYCLITOLS 
  183893. 1994 X
  183894. 4706Y
  183895. 13148
  183896. HURTAUD, D.
  183897. 14157N
  183898. 2/28/96
  183899. CHEMOSELECTIVE NUCLEOPHILIC ATTACK OF A,A
  183900. DICYANO EPOXIDES: A SIMPLE SYNTHESIS OF A
  183901. AMINO AMIDES, EPOXY AMIDINES AND THEIR CYCLIC ANALOGS
  183902. 1994X    4701
  183903. 4703Y
  183904. 13149
  183905. VASUDEVAN, S.
  183906. 14158N
  183907. 2/28/96
  183908. AUDIASTEREOSELECTIVITY IN THE PATERNO
  183909. CHI REACTION OF ENOL ACETATES AND BENZALDEHYDES
  183910. 1994 X    4677
  183911. 4679Y
  183912. 13150
  183913. ARMESTO, X. L.
  183914. JOCCSMODEL SOLUTIONS WASTE
  183915. WATER CHLORINATION CHLOROALDIMINES SYNCHRONIZATION PRINCIPLE M
  183916. 14159N
  183917. 2/28/96
  183918. AACONCERTED GROB FRAGMENTATION IN N
  183919. AMINO ACID DECOMPOSITION
  183920. 1994X    4659
  183921. 4664Y
  183922. 13151
  183923. PASTO, D. J.
  183924. CHAIN ADDITION BENZENETHIOL M
  183925. 14160N
  183926. 2/28/96
  183927. A STUDY OF THE REGIOSELECTIVITY OF THE RADICAL ADDITION OF ''RSAR'' DERIVED FROM THE PHOTOLYSIS OF TERT
  183928. HOMOALLYL AND TERT
  183929. ALKYL 4
  183930. NITROBENZENESULFENATES TO SUBSTITUTED ALLENES AND ALKENES
  183931. 1994X    4642
  183932. 4646Y
  183933. 13152
  183934. RITTER, A. R.
  183935. JOCC,REDUCTIVE CLEAVAGE CYCLOADDITIONS ALKALOIDS M
  183936. 14161N
  183937. 2/28/96
  183938. AuAMINO ACID
  183939. DERIVED CHIRAL ACYL NITROSO COMPOUNDS: DIASTEREOSELECTIVITY IN INTERMOLECULAR HETERO DIELS
  183940. ALDER REACTIONS
  183941. 1994 X    4602
  183942. 4611Y
  183943. 13153
  183944. A    SAMES, D.
  183945. HIGHLY STEREOSELECTIVE SYNTHESIS OSMIUM
  183946. TETROXIDE OXIDATION ALLYLIC ALCOHOL SYSTEMS ORGANIC
  183947. SYNTHESIS NEOCARZINOSTATIN CHROMOPHORE ASYMMETRIC DIHYDROXYLATION AMINO
  183948. ACIDS DERIVATIVES CHEMISTRY STEREOCHEMISTRY M
  183949. 14162N
  183950. 2/28/96
  183951. AUAN ENANTIOSELECTIVE SYNTHESIS OF N
  183952. METHYLFUCOSAMINE VIA TANDEM C
  183953. O BOND FORMATION
  183954. 1994 X    4596
  183955. 4601Y
  183956. 13154
  183957. DENMARK, S. E.
  183958. DIELS
  183959. ALDER REACTIONS TANDEM INTER <4 PYRROLIDINES ACID OLEFINS (+/
  183960. HAEMANTHIDINE (+/
  183961. PRETAZETTINE CONFORMATIONS CONSTRUCTION CYCLIZATIONS M
  183962. 14163N
  183963. 2/28/96
  183964. NITROALKENE [4+2] CYCLOADDITIONS WITH 2
  183965. (ACYLOXY)VINYL ETHERS. STEREOSELECTIVE SYNTHESIS OF 3
  183966. HYDROXY
  183967. SUBSTITUTED
  183968. PYRROLIDINES
  183969. 1994X    4576
  183970. 4595Y
  183971. 13155
  183972. KATRITZKY, A. R.
  183973. SYNTHETIC APP LICATIONS 2
  183974. DIENES REACTIVITY AMINES ROUTE BIS(IMINOPHOSPHORANES) 2
  183975. BUTADIENES OLEFINATION CARBANIONS CONVERSION M
  183976. 14164N
  183977. 2/28/96
  183978. CONVENIENT PREPARATIONS OF DIETHYL [(ACYLAMINO)METHYL]PHOSPHONATES, 2
  183979. AZABUTADIENES, AND ISOQUINOLINES FROM A 1,2
  183980. MONOAZABISYLIDE EQUIVALENT
  183981. 1994 X    4556
  183982. 4560Y
  183983. 13156
  183984. KATRITZKY, A. R.
  183985. JOCCeONE
  183986. POT PREPARATION SYNTHETIC APP LICATIONS BIS(IMINOPHOSPHORANES) AMINES ROUTE EQUIVALENT EFFICIENT M
  183987. 14165N
  183988. 2/28/96
  183989. BIS(TRIPHENYLPHOSPHORANYLIDENE)PROPANE: A NOVEL =CHCH2N= SYNTHON
  183990. 1994X    4551
  183991. 4555Y
  183992. 13157
  183993. UESAKA, N.
  183994. METAL
  183995. PROMOTED CYCLIZATION FORMAL TOTAL SYNTHESIS BOND
  183996. FORMING REACTION MAGNESIUM REAGENTS GRIGNARD
  183997. REAGENTS ETHYLMAGNESATION DERIVATIVES ALKENES CARBOMAGNESATION BICYCLIZATION M
  183998. 14166N
  183999. 2/28/96
  184000. AKNOVEL SYNTHESIS OF HETEROCYCLES USING ZIRCONIUM
  184001. CATALYZED DIENE CYCLIZATION
  184002. 1994 X    4542
  184003. 4547Y
  184004. 13158
  184005. DAVIES, H. M. L.
  184006. JOCC\CYCLOPROPANATION COPE REARRANGEMENT ALPHA
  184007. DIAZO KETONES CYCLOPROPENES REAGENTS ESTERS METAL M
  184008. 14167N
  184009. 2/28/96
  184010. APCARBENOID VERSUS VINYLOGOUS REACTIVITY IN RHODIUM(II)
  184011. STABILIZED VINYLCARBENOIDS
  184012. 1994X    4535
  184013. 4541Y
  184014. 13159
  184015. MCALLISTER, M. A.
  184016. MICROWAVE
  184017. SPECTRUM GROUP ELECTRONEGATIVITIES ABINITIO CALCULATIONS DOUBLE
  184018. BONDS ENERGIES STABILITY STABILIZATION DERIVATIVES VINYL PHOTOELECTRON M
  184019. 14168N
  184020. 2/28/96
  184021. COMPARATIVE CUMULENE SUBSTITUENT EFFECTS: KETENES, ALLENES, DIAZOMETHANES, DIAZIRINES, AND CYCLOPROPENES BY AB INITIO MOLECULAR ORBITAL CALCULATIONS
  184022. 1994 X    4506
  184023. 4515Y
  184024. 13160
  184025. RODRIGUEZ, C. M.
  184026. FERROELECTRIC LIQUID
  184027. CRYSTALS ENANTIOSELECTIVE SYNTHESIS EFFICIENT OXIDATION KINETIC RESOLUTION TRANSITION
  184028. STATES CARBOXYLIC
  184029. ACIDS ALLYLIC ALCOHOLS RING EXPANSION CHIRAL DOPANTS GROUND
  184030. STATES M
  184031. 14169N
  184032. 2/28/96
  184033. STEREOSELECTIVE SYNTHESIS OF HIGHLY SUBSTITUTED g
  184034. LACTONES AND BUTENOLIDES BY INTRAMOLECULAR MICHAEL ADDITION OF ENANTIOMERICALLY ENRICHED g
  184035. [(PHENYLTHIO)ACYL]OXY A,b
  184036. UNSATURATED ESTERS
  184037. 1994 X    4461
  184038. 4472Y
  184039. 13161
  184040. BRANALT, J.
  184041. JOCCYBIOLOGICAL
  184042. ACTIVITY 2,3
  184043. EPOXY ALCOHOLS 4'
  184044. THIO ANALOGS NUCLEOSIDES DERIVATIVES ROUTE HIV M
  184045. 14170N
  184046. 2/28/96
  184047. AlA NEW SYNTHESIS OF 4
  184048. THIOFURANOSIDES VIA REGIOSELECTIVE OPENING OF AN EPISULFIDE WITH ALLYLMAGNESIUM BROMIDE
  184049. 1994 X    4430
  184050. 4432Y
  184051. 13162
  184052. BOTO, A.
  184053. RING EXPANSION INTRAMOLECULAR FUNCTIONALIZATION PROSTAGLANDIN BIOSYNTHESIS MITSUNOBU REACTION MOLECULAR
  184054. OXYGEN CYCLIC PEROXIDES CYCLIZATION MECHANISM VINYLCYCLOPROPANES STEREOCHEMISTRY M
  184055. 14171N
  184056. 2/28/96
  184057. AWFRAGMENTATION OF ALKOXY RADICALS: TANDEM b
  184058. FRAGMENTATION
  184059. CYCLOPEROXYIODINATION REACTION
  184060. 1994 X    4393
  184061. 4401Y
  184062. 13163
  184063. BRANDES, B. D.
  184064. JACOBSEN B
  184065. UNFUNCTIONALIZED OLEFINS ASYMMETRIC EPOXIDATION PORPHYRINS COMPLEXES 
  184066. CHIRAL EPOXIDE EPOXIDATION SALEN MANGANESE COMPLEX ENANTIOSELECTIVE ASYMMETRICM
  184067. 14172N
  184068. 2/28/96
  184069. AHHIGHLY ENANTIOSELECTIVE, CATALYTIC EPOXIDATION OF TRISUBSTITUTED OLEFINS
  184070. 1994X    4378
  184071. 4380Y
  184072. 13164
  184073. A    SAITO, S.
  184074. NUCLEOSIDE DERIVATIVES SERIES 
  184075. NITRONE DIPOLAR
  184076. CYCLOADDITION CHIRAL DIOL TRANSITION STATE DIASTEREOSELECTIVITY ASYMMETRIC CONTROLLERM
  184077. 14173N
  184078. 2/28/96
  184079. ROLE OF A PROTECTED VICINAL DIOL CONTROLLER IN INTRAMOLECULAR [3+2] CYCLOADDITION REACTIONS OF CHIRAL ACYCLIC ALKENYL NITRONES: SYNTHESES OF ENANTIOMERICALLY PURE TETRASUBSTITUTED CYCLOBUTYLAMINES
  184080. 1994 X    4375
  184081. 4377Y
  184082. 13165
  184083. HALE, M. R.
  184084. INTRAMOLECULAR HYDROSILATION SILAFUNCTIONAL COMPOUNDS ORGANIC
  184085. SYNTHESIS LITHIUM DIMETHYLCUPRATE RADICAL CYCLIZATION PI
  184086. COMPLEX STEREOCONTROL ACID OLEFINS EPOXIDATION M
  184087. 14174N
  184088. 2/28/96
  184089. DIASTEREOSELECTIVE HETEROATOM
  184090. DIRECTED CONJUGATE ADDITION OF SILYLCUPRATE REAGENTS TO UNSATURATED CARBONYLS. A STEREOSELECTIVE ROUTE TO b
  184091. CARBONYL SILOXANES
  184092. 1994X    4370
  184093. 4374Y
  184094. 13166
  184095. Lee, S. J.B
  184096. 14175N
  184097. 2/28/96
  184098. BUTADIENYL)PYRIDINIUM BROMIDE, A NOVEL DIENE IN DIELS
  184099. ALDER REACTIONS
  184100. 1994 X    4367
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  184102. 13167
  184103. WASSERMAN, H. H.
  184104. SPONGE THEONELLA SP PEPTIDYL FLUOROMETHYL KETONES BIOACTIVE MARINE METABOLITES HUMAN NEUTROPHIL ELASTASE PROTECTED AMINO
  184105. ACIDS THROMBIN INHIBITORS HYDROLYTIC ENZYMES CATHEPSIN
  184106. G HUMAN RENIN DERIVATIVES M
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  184108. 2/28/96
  184109. A~(CYANOMETHYLENE)PHOSPHORANES AS NOVEL CARBONYL 1,1
  184110. DIPOLE SYNTHONS: AN EFFICIENT SYNTHESIS OF A
  184111. KETO ACIDS, ESTERS, AND AMIDES
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  184114. 13168
  184115. NAKATANI, K.
  184116. C4ANTITUMOR ANTIBIOTICS KAPURIMYCINS STREPTOMYCES DNA M
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  184118. 2/28/96
  184119. HIGHLY EFFICIENT SYNTHESIS OF 2
  184120. SUBSTITUTED 4H
  184121. CHROMEN
  184122. ONES BY MEANS OF F 
  184123. INDUCED 6
  184124. DIGONAL CYCLIZATION OF O
  184125. (SILYLOXY)PHENYL ETHYNYL KETONE DERIVATIVES
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  184128. 13169
  184129. SEMMELHACK, M. F.
  184130. JOCCYCALICHEAMICIN CHROMOPHORE CHEMISTRY BINDING ANTIBIOTICS SPECIFICITY BIOLOGY COMPLEX CORE M
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  184132. 2/28/96
  184133. A^THE EFFECT ON DNA CLEAVAGE POTENCY OF TETHERING A SIMPLE CYCLIC ENEDIYNE TO A NETROPSIN ANALOG
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  184135. 4359Y
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  184138. JOCC7CATALYTIC ASYMMETRIC EPOXIDATION ACYLSILANES CHEMISTRY M
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  184140. 2/28/96
  184141. SYNTHESIS OF OPTICALLY ACTIVE 2,3
  184142. ISOPROPYLIDENE
  184143. (TRIMETHYLSILYL)GLYCERALDEHYDE AND OTHER DERIVATIVES OF (A
  184144. HYDROXYACYL)SILANE
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  184147. 13171
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  184150. TRANSCRIPTASE HETEROCYCLIC QUINONES STREPTONIGRIN VIRUS M
  184151. 14180N
  184152. 2/28/96
  184153. AsSYNTHESIS OF 4
  184154. HYDROXY AND 4
  184155. ALKOXYQUINOLINEQUINONES USING OXIDATIVE DEMETHYLATION WITH CERIUM(IV) AMMONIUM NITRATE
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  184161. BIS(TRIFLUOROMETHYL)
  184162. 1,2,4,5
  184163.  TETRAZINE M
  184164. 14181N
  184165. 2/28/96
  184166. INVERSE
  184167. ELECTRON
  184168. DEMAND DIELS
  184169. ALDER REACTIONS OF CONDENSED PYRIDAZINES .4. SYNTHESIS AND CYCLOADDITION REACTIONS OF 1,4
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  184180. ABA NEW ENTRY TO 5
  184181. UNSUBSTITUTED 3
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  184191. AnFORMYLATION OF 2,5
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  184204. AdINTRAMOLECULAR SULFENYLATION USING SULFOXIDES 
  184205.  PREPARATION OF 5H
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  184219. DIASTEREOSELECTIVE ADDITION OF ALLYLTRIPHENYL
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  184221. SULFINYLFURFURAL MEDIATED BY TITANIUM(IV) TETRACHLORIDE AND TIN(IV) TETRACHLORIDE
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  184229. AEAN EXPEDIENT PALLADIUM
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  184261. ISOCOMENE (+1
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  184326. BRIDGEHEAD CARBOCATIONS: FORMATION OF A 1
  184327. BICYCLO[2.1.1]HEXYL CATION AS THE PRIMARY INTERMEDIATE IN THE SOLVOLYSIS OF 3
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  184337. AyINTRAMOLECULAR AMINATION OF OLEFINS. SYNTHESIS OF 2
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  184350. BENZENESULFONYL
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  184405. A`ENOL TRIFLATE PYRANOSES, VERSATILE REAGENTS FOR THE FORMATION OF CONJUGATED SYSTEMS ON PYRANOSES
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  184523. A:CARBOCYCLIZATION OF d
  184524. ACETYLENIC PROPARGYLIC ZINC REAGENTS
  184525. 1994X    5645
  184526. 5648Y
  184527. 13201
  184528. DECHOUX, L.
  184529. Tet. Lett.C
  184530. ORGANIC
  184531. SYNTHESIS K
  184532. BASIC INTRAMOLECULAR RING OPENING REACTIONS OF VICINALLY SUBSTITUTED ACCEPTOR
  184533. DONNOR (TRANS)
  184534. CYCLOPROPANES WERE STUDIED. AN APP LICATION TO THE DIASTEREOSELECTIVE SYNTHESIS OF (CIS)
  184535. HYDROXYMETHYLCYCLOPROPANES IS PRESENTED.M
  184536. 14210N
  184537. 2/28/96
  184538. DIASTEREOCONTROL IN THE OPENING OF VIC
  184539. ACCEPTOR
  184540. DONOR CYCLOPROPANES. APPLICATION TO THE SYNTHESIS OF (CIS) 1
  184541. HYDROXYMETHYLCYCLOPROPANES
  184542. 1994 X    5633
  184543. 5636Y
  184544. 13202
  184545. BOIVIN, J.
  184546. Tet. Lett.CvCHAIN
  184547. REACTIONS ORGANIC
  184548. SYNTHESIS CYCLIZATION ALPHA (+/
  184549. MESEMBRANOL 5
  184550. TRIG TEMPERATURE COMPLEXES AMIDES DESIGN K
  184551. A VARIETY OF GAMMA
  184552. LACTAMS ARE OBTAINED FROM SUITABLE OF ALPHA
  184553. HALOAMIDES BY A RADICAL CYCLISATION MEDIATED BY A COMBINATION OF NICKEL POWDER AND ACETIC ACID.M
  184554. 14211N
  184555. 2/28/96
  184556. APA VERSATILE RADICAL BASED SYNTHESIS OF g
  184557. LACTAMS USING NICKEL POWDER ACETIC ACID
  184558. 1994 X    5629
  184559. 5632Y
  184560. 13203
  184561. DESHPANDE, M. S.
  184562. Tet. Lett.CGPROTECTED PEPTIDE
  184563. FRAGMENTS PHASE SYNTHESIS GENERATION DIVERSITY RESIN 
  184564. VINYL/ARYL STANNANES COUPLE SMOOTHLY WITH POLYMER BOUND ARYL IODIDES. THE CROSS
  184565.  COUPLED PRODUCTS ARE OBTAINED IN EXCELLENT YIELD AND PURITY AFTER CLEAVAGE FROM THE SOLID SUPPORT.M
  184566. 14212N
  184567. 2/28/96
  184568. ATFORMATION OF CARBON
  184569. CARBON BOND ON SOLID SUPPORT: APPLICATION OF THE STILLE REACTION
  184570. 1994 X    5613
  184571. 5614Y
  184572. 13204
  184573. AUGERI, D. J.
  184574. Tet. Lett.C
  184575. IONOMYCIN KETONES 
  184576. ;THE ALKYLATION OF C
  184577. SYMMETRIC N
  184578. AMINOAZIRIDINYLHYDRAZONE ANIONS SHOWS EXCELLENT DIASTEREOSELECTIVITY DESPITE THE ABSENCE OF CHELATING GROUPS IN THE CHIRAL AUXILIARY. IN CONTRAST TO OTHER DIALKYLHYDRAZONES, AZIRIDINYLHYDRAZONES EXHIBIT A SYN
  184579. DIRECTING EFFECT ANALOGOUS TO THAT OBSERVED FOR ARENESULFONYLHYDRAZONES.
  184580. 14213N
  184581. 2/28/96
  184582. AMINOAZIRIDINYLHYDRAZONES: HIGHLY DIASTEREOSELECTIVE ALKYLATION WITHOUT CHELATION, AND A SYN
  184583. DIRECTING EFFECT
  184584. 1994 X    5599
  184585. 5602Y
  184586. 13205
  184587. KUMAR, A.
  184588. DITTMER 
  184589. Tet. Lett.CCTELLURIDE EPOXIDE RING OPENING CHIRAL ALCOHOL STEREOCHEM ASYMMETRIC
  184590. AS LITTLE AS 0.1 MOLAR EQUIVALENT OF ELEMENTAL TELLURIUM IN COMBINATION WITH EXCESS (UP TO 3 MOLAR EQUIVALENTS) REDUCING AGENT (HOCH2SO2NA.2H2O, NABH4, OR LIET(3)BH) EFFECTS THE TELLURIDE
  184591. ION MEDIATED TRANSPOSITION OF ALLYLIC HYDROXYL GROUPS AND CARBON
  184592. CARBON DOUBLE BONDS THAT PROCEEDS VIA THE EPOXY TOSYLATE. THE WORKUP IS MUCH MORE CONVENIENT THAN WHEN A MOLAR EQUIVALENT OF TELLURIUM IS USED.
  184593. 14214N
  184594. 2/28/96
  184595. AmA CATALYTIC TELLURIUM PROCESS FOR THE TRANSPOSITION OF ALLYLIC HYDROXYL GROUPS AND CARBON
  184596. CARBON DOUBLE BONDS
  184597. 1994 X    5583
  184598. 5586Y
  184599. 13206
  184600. LIPSHUTZ, B. H.
  184601. Tet. Lett.C
  184602. ESTERIFICATION OFFICINALIS 
  184603. GENERATION OF AN INTRAMOLECULARLY TETHERED, NONRACEMIC DIARYL CUPRATE FOLLOWED BY ITS OXIDATION WITH GROUND STATE OXYGEN AT 
  184604. 78 DEGREES LEADS TO A BIARYL PRECURSOR TO AN ELLAGITANNIN. SUBSEQUENT ATTACHMENT OF THE APP ROPRIATE GLUCOSE UNIT COMPLETES THE SYNTHESIS OF THE TITLE COMPOUND.
  184605. 14215N
  184606. 2/28/96
  184607. CYANOCUPRATE
  184608. MEDIATED INTRAMOLECULAR BIARYL COUPLINGS APPLIED TO AN ELLAGITANNIN. SYNTHESIS OF (+)
  184609. PERMETHYLTELLIMAGRANDIN II
  184610. 1994X    5567
  184611. 5570Y
  184612. 13207
  184613. DOWD, P.
  184614. Tet. Lett.
  184615. EXPANSION FUSED CYCLOBUTANONES BICYCLIC SYSTEMS GROUP MIGRATION FRAGMENTATION CONSTRUCTION CYCLIZATION ADDITIONS CLEAVAGE CYANO 
  184616. CHLORO TIN CYCLIZATION NOVEL BRIDGED ADDITION ALKENE INTRAMOLECULAR CARBONYL RADICALK
  184617. FREE RADICAL REACTION OF ENDO
  184618. HAROALKYLBICYCLO[4.2.0]OCT
  184619. ONES 1 AND 11 LEADS TO SEQUENTIAL REARRANGEMENT AND FORMATION OF THE NOVEL, BRIDGED TRICYCLIC KETONES 2 AND 13. A MECHANISM FOR THIS UNUSUAL TRANSFORMATION IS PROPOSED.M
  184620. 14216N
  184621. 2/28/96
  184622. A7A CYCLOBUTANONE
  184623. BASED TANDEM FREE RADICAL REARRANGEMENT
  184624. 1994X    5563
  184625. 5566Y
  184626. 13208
  184627. A    SPINO, C.
  184628. Tet. Lett.C
  184629. CONVENIENT SYNTHESIS 2
  184630. CARBOMETHOXY
  184631. BUTADIENE PRECURSOR 
  184632. INTRAMOLECULAR NATURAL PRODUCT TARGET TETHERED CASCADE ALKYNE STEREOCHEM
  184633. A NOVEL AND EFFICIENT STEREOSELECTIVE SYNTHESIS OF THE PERHYDROPHENANTHRENE SKELETON WAS ACHIEVED USING A SEQUENTIAL DIELS
  184634. ALDER CYCLOADDITION STRATEGY INVOLVING ENYNE 10 AND BIS
  184635. DIENE 8.M
  184636. 14217N
  184637. 2/28/96
  184638. ApAN EXPEDIENT AND STEREOSELECTIVE ROUTE TO THE PERHYDROPHENANTHRENE SKELETON VIA SEQUENTIAL DIELS
  184639. ALDER REACTIONS
  184640. 1994 X    5559
  184641. 5562Y
  184642. 13209
  184643. HONG, Y. P.
  184644. Tet. Lett.CJBETA
  184645. AMINO ALCOHOLS ENANTIOSELECTIVE REDUCTION KETONES BORANE ENANTIOMERS K
  184646. ASYMMETRIC BORANE REDUCTION OF ALPHA
  184647. KETOIMINES WITH OXAZABOROLIDINE CATALYSTS HAS BEEN STUDIED. THE EE'S OF THE RESULTING ARYLETHANOLAMINES ARE UP TO 93% USING 20% MOL% OF THE CATALYST.
  184648. 14218N
  184649. 2/28/96
  184650. A|ASYMMETRIC REDUCTION OF A
  184651. KETOIMINES WITH OXAZABOROLIDINE CATALYSTS: A NOVEL, PRACTICAL APPROACH TO CHIRAL ARYLETHANOLAMINES
  184652. 1994 X    5551
  184653. 5554Y
  184654. 13210
  184655. RICHTER, L. S.
  184656. Tet. Lett.CbPEPTIDE CYCLIZATIONS SOLID SUPP ORT BOC
  184657. CHEMISTRY POLYMER
  184658. BOUND OXIME CYCLIC
  184659. PEPTIDES RESIN MODEL 
  184660. A SERIES OF CYCLIC PENTA
  184661. , HEXA
  184662.  AND HEPTAPEPTIDES WAS SYNTHESIZED USING A NOVEL CYCLIZATION STRATEGY. AFTER ATTACHMENT OF THE FIRST AMINO ACID TO THE SOLID SUPP ORT WITH A THIOESTER
  184663. LINKAGE, THE LINEAR PEPTIDES WERE SYNTHESIZED USING BOC
  184664. CHEMISTRY. HEAD
  184665. TAIL CYCLIZATIONS WERE PERFORMED ON THE SOLID SUPP ORT AND PROVIDED THE DESIRED CYCLOPEPTIDES IN HIGH PURITY AND GOOD YIELDS.
  184666. 14219N
  184667. 2/28/96
  184668. AXPEPTIDE
  184669. CYCLIZATIONS ON SOLID SUPPORT: A FAST AND EFFICIENT ROUTE TO SMALL CYCLOPEPTIDES
  184670. 1994X    5547
  184671. 5550Y
  184672. 13211
  184673. A    Wu, Z. Y.B
  184674. Tet. Lett.C
  184675. ACID 
  184676. "IODINE PROMOTED DECOMPOSITION OF 1
  184677. DIALKYLTRIAZENES IN ORGANIC SOLVENTS IS SHOWN TO GIVE HIGH YIELDS OF THE CORRESPONDING ARYL IODIDES UNDER EXTREMELY MILD CONDITIONS. THE PRESENCE OF IODINE GREATLY ACCELERATES THE REACTION IN BOTH IODOALKANES AS WELL AS IN NON
  184678. IODINATED SOLVENTS.
  184679. 14220N
  184680. 2/28/96
  184681. AmIODINE
  184682. PROMOTED DECOMPOSITION OF 1
  184683. DIALKYLTRIAZENES: A MILD METHOD FOR THE SYNTHESIS OF ARYL IODIDES
  184684. 1994  X    5539
  184685. 5542Y
  184686. 13212
  184687. MAIKAP, G. C.
  184688. TetrahedronC
  184689. ALLYLIC ALKYLATIONS 
  184690. CATALYTIC AMOUNT OF COBALT(II) CHLORIDE IN 1,2
  184691. DICHLOROETHANE PROMOTES THE ALLYLATION OF 1,3
  184692. DICARBONYL COMPOUNDS WITH ALLYL ACETATES IN HIGH YIELDS. THE ALLYLATION OF PENTANE
  184693. DIONE IS HIGHLY REGIOSELECTIVE AS COMPARED WITH METHYLACETOACETATE AND ETHYL 2
  184694. OXOCYCLOPENTANECARBOXYLATE.
  184695. 14221N
  184696. 2/28/96
  184697. AFCOBALT CATALYZED REGIOSELECTIVE ALLYLATION OF 1,3
  184698. DICARBONYL COMPOUNDS
  184699. 1994 X    9145
  184700. 9156Y
  184701. 13213
  184702. A    JI, J. G.
  184703. TetrahedronC'EFFICIENT SYNTHESIS ACETYLENES ALKYNES 
  184704. ALPHA
  184705.  AND (E)
  184706.  CHTOROALKYLIDENE
  184707. GAMMA
  184708. BUTYROLACTONE BETA
  184709. ACETIC ACID DERIVATIVES WERE PREPARED FROM EASILY AVAILABLE ACYCLIC ALLYLIC 2
  184710. ALKYNOATES USING PD
  184711. 2(DBA)(3) CHCL3 AS CATALYST UNDER 1 ATM OF CO IN THE PRESENCE OF CUCL2 AND LICL IN HIGH STEREOSELECTIVITY.
  184712. 14222N
  184713. 2/28/96
  184714. PALLADIUM CATALYZED CYCLIZATION
  184715. CARBONYLATION OF ALLYLIC 2
  184716. ALKYNOATES: FACILE SYNTHESIS OF A
  184717. ALKYLIDENE
  184718. BUTYROLACTONE b
  184719. ACETIC ACID DERIVATIVES
  184720. 1994X    9067
  184721. 9078Y
  184722. 13214
  184723. Ye, B.B
  184724. TetrahedronK
  184725. A DETAILED STUDY ON THE REACTIONS OF SEVERAL KETONES WITH METHYL METHACRYLATE IN THE PRESENCE OF LITHIUM HEXAMETHYLDISILAMIDE HAS BEEN REPORTED.M
  184726. 14223N
  184727. 2/28/96
  184728. AYTANDEM SYNTHESES OF CYCLOHEXANE DERIVATIVES VIA SEQUENTIAL MICHAEL
  184729. MICHAEL
  184730. ALDOL REACTION
  184731. 1994 X    9061
  184732. 9066Y
  184733. 13215
  184734. DUJARDIN, G.
  184735. TetrahedronC
  184736. DIELS
  184737. ALDER
  184738. REACTIONS ENOL ETHERS DENOVO
  184739. SYNTHESIS NATURAL
  184740. PRODUCTS CYCLOADDITIONS HIGH
  184741. PRESSURE DIENOPHILES DERIVATIVES AUXILIARIES INDUCTION 
  184742. THE ALKYL VINYL ETHERS 2B
  184743. 8B (DERIVING FROM THE ALCOHOLS 2A
  184744. 8A) SMOOTHLY REACTED WITH METHYL E
  184745. BENZYLIDENEPYRUVATE 10 IN THE PRESENCE OF CATALYTIC AMOUNTS OF EU(FOD)(3) OR YB(FOD)(3) IN REFLUXING HEXANE, THUS LEADING TO THE DIHYDROPYRAN ENDO ADDUCTS 13
  184746. 19 IN HIGH YIELDS (80
  184747. 95%). THE ENDO
  184748. CYCLOADDUCTS 13
  184749. 17 WERE OBTAINED WITH DIASTEREOFACIAL SELECTIVITIES (DS) RANGING FROM 76/24 TO 87.5/12.5. ASYMMETRIC INDUCTION WAS FOUND TO CULMINATE WITH THE VINYL ETHER (
  184750. 7B DERIVING FROM N
  184751. BUTYL (R)
  184752. MANDELATE : THE BEST DS (92.5/7.5) WAS OBTAINED FOR THE
  184753. 14224N
  184754. 2/28/96
  184755. ASYMMETRIC SYNTHESIS AND ABSOLUTE CONFIGURATION OF SUBSTITUTED DIHYDROPYRANS, BY INTRAMOLECULAR HETEROCYCLOADDITION OF CHIRAL VINYL ETHERS
  184756. 1994 X    9037
  184757. 9050Y
  184758. 13216
  184759. TOSHIMITSU, A.
  184760. TetrahedronC
  184761. OPTICALLY
  184762. ACTIVE EPOXIDES EPISULFONIUM IONS NUCLEOPHILIC
  184763. ATTACK GENERAL
  184764. METHOD OLEFINS SULFIDES CARBOSULFENYLATION STEREOCHEMISTRY CYCLIZATIONS CARBOCYCLES 
  184765. IN CHIRAL ALCOHOLS BEARING A PHENYLTHIO GROUP AT THE BETA CARBON ATOM, THE HYDROXY GROUP IS REPLACED BY NITRILES THROUGH THE ANCHIMERIC ASSISTANCE OF THE PHENYLTHIO GROUP TO AFFORD CHIRAL AMIDES WITH RETENTION OF CONFIGURATION. THIS STEREOSPECIFIC RITTER
  184766. TYPE REACTION HAS BEEN UTILIZED IN THE CONVERSION OF CHIRAL GLYCIDOL DERIVATIVES TO CHIRAL CYCLIC IMINO ETHERS SUCH AS OXAZOLINES BEARING AN ARYLTHIO GROUP.
  184767. 14225N
  184768. 2/28/96
  184769. RETENTION OF CONFIGURATION IN THE RITTER
  184770. TYPE SUBSTITUTION REACTION OF CHIRAL b
  184771. ARYLTHIO ALCOHOLS THROUGH THE ANCHIMERIC ASSISTANCE OF THE ARYLTHIO GROUP
  184772. 1994X    8997
  184773. 9008Y
  184774. 13217
  184775. A    BESSE, P.
  184776. TetrahedronM
  184777. 14226N
  184778. 2/28/96
  184779. A4CHEMICAL AND BIOLOGICAL SYNTHESIS OF CHIRAL EPOXIDES
  184780. 1994 X    8885
  184781. 8927Y
  184782. 13218
  184783. WERNER, H.
  184784. J. Organomet. Chem.CTRHODIUM CATALYSIS OLEFIN SUPP ORTED CATALYST METAL
  184785. COMPLEXES DERIVATIVES SILICA GEL M
  184786. 14227N
  184787. 2/28/96
  184788. AySUPPORTED RHODIUM CATALYSTS 
  184789.  NEW ASPECTS IN THE FORMATION OF TRISUBSTITUTED OLEFINS FROM SIMPLE ALKENES AND DIAZOALKANES
  184790. 1994 X
  184791. PP 277
  184792. 13219
  184793. BENCZE, L.
  184794. J. Organomet. Chem.CiTUNGSTEN ABINITIO CARBENE MOLECULAR MECHANICS OLEFIN METATHESIS DOUBLE
  184795. BOND TUNGSTEN COMPLEXES CATALYSTS M
  184796. 14228N
  184797. 2/28/96
  184798. AkMOLECULAR MECHANICAL STUDIES ON THE OLEFIN METATHESIS REACTION .3. MODELLING OF THE 'WELL
  184799. DEFINED' CARBENES
  184800. 1994X
  184801. PP 183
  184802. 13220
  184803. STAFFORD, J. A.
  184804. 14229N
  184805. 2/28/96
  184806. AdA UNIFIED STRATEGY FOR THE SYNTHESIS OF HIGHLY SUBSTITUTED DIHYDROBENZOFURANS AND DIHYDROBENZOPYRANS
  184807. 1994 X    4346
  184808. 4349Y
  184809. 13221
  184810. WEIDNER, C. H.
  184811. 14230N
  184812. 2/28/96
  184813. ABCONVENIENT AND GENERAL SYNTHESIS OF 2
  184814. ALKOXY
  184815. ARYLCYCLOPROPENONES
  184816. 1994 X    4319
  184817. 4322Y
  184818. 13222
  184819. PEPITO, A. S.
  184820. 14231N
  184821. 2/28/96
  184822. AvAPPLICATION OF TELLURIUM CHEMISTRY AND SHARPLESS ASYMMETRIC EPOXIDATION TO THE SYNTHESIS OF OPTICALLY ACTIVE BOIVINOSE
  184823. 1994X    4311
  184824. 4312Y
  184825. 13223
  184826. PARAKKA, J. P.
  184827. 14232N
  184828. 2/28/96
  184829. A2NOVEL O
  184830. QUINODIMETHANE TANDEM DIELS
  184831. ALDER REACTION
  184832. 1994 X    4308
  184833. 4310Y
  184834. 13224
  184835. LABADIE, S. S.
  184836. JOCC}CROSS
  184837. COUPLING REACTION ORGANIC ELECTROPHILES ORGANOTIN REAGENTS PROTECTING GROUP PYRROLES ORGANOSTANNANES DERIVATIVES ACIDS M
  184838. 14233N
  184839. 2/28/96
  184840. AIINDOL
  184841. YLTRIBUTYLSTANNANE: A VERSATILE REAGENT FOR 2
  184842. SUBSTITUTED INDOLES
  184843. 1994 X    4250
  184844. 4254Y
  184845. 13225
  184846. ECHAVARREN, A. M.
  184847. ENANTIOMERICALLY PURE DIHYDROPYRIMIDINONES ORGANOTIN COMPOUNDS GAMMA
  184848. ALPHA, BETA
  184849.  UNSATURATED MACROCYCLES ALPHA,BETA
  184850. UNSATURATED KETONES CONVENIENT SYNTHESIS DICARBONYL
  184851. COMPOUNDS ASYMMETRIC
  184852. SYNTHESIS CONJUGATE ADDITION OXIDATIVE ADDITION FACILE SYNTHESIS 
  184853. 14234N
  184854. 2/28/96
  184855. PALLADIUM
  184856. CATALYZED REDUCTIVE COUPLING OF ACID CHLORIDES WITH b
  184857. STANNYL ENONES: SYNTHESIS OF 1,4
  184858. DIKETONES AND MECHANISTIC ASPECTS
  184859. 1994 X    4179
  184860. 4185Y
  184861. 13226
  184862. LAROCK, R. C.
  184863. SUBSTITUTED ARYL HALIDES STEREOSELECTIVE SYNTHESIS NITROGEN
  184864. HETEROCYCLES ALLYLIC SUBSTITUTION CYCLIZATIONS HETEROANNULATION CONSTRUCTION ALKYNES IODIDES AMINES M
  184865. 14235N
  184866. 2/28/96
  184867. AwSYNTHESIS OF PYRROLIDINES AND PIPERIDINES VIA PALLADIUM
  184868. CATALYZED COUPLING OF VINYLIC HALIDES AND OLEFINIC SULFONAMIDES
  184869. 1994 X    4172
  184870. 4178Y
  184871. 13227
  184872. A    BLOCH, R.
  184873. FACIAL DIASTEREOSELECTION LEWIS ACID ALLYLIC SUBSTITUENTS TRANSITION STRUCTURES STEREOGENIC CENTER FACE SELECTIVITY CYCLOADDITIONS DIENES ACROLEIN 2
  184874. LITHIO
  184875. BUTADIENE M
  184876. 14236N
  184877. 2/28/96
  184878. THERMAL AND CATALYZED DIELS
  184879. ALDER REACTIONS WITH CHIRAL 2
  184880. SUBSTITUTED
  184881. DIENES: CONFORMATIONAL MODELS FOR DIASTEREOFACIAL SELECTIVITY
  184882. 1994 X    4162
  184883. 4169Y
  184884. 13228
  184885. A    MAREK, I.
  184886. CARBON BOND FORMATION DIMETALLIC ORGANIC
  184887. COMPOUNDS TRANSITION
  184888. METAL CATALYSIS ENOLATE CLAISEN REARRANGEMENT ALLYLIC GRIGNARD
  184889. REAGENTS VINYL
  184890. COPP ER DERIVATIVES ORGANOMETALLIC COMPOUNDS ENE REACTIONS STEREOSELECTIVE SYNTHESIS STEREOCHEMICAL CONTROL M
  184891. 14237N
  184892. 2/28/96
  184893. A1DIASTEREOSELECTIVE CARBOMETALATION OF VINYLMETALS
  184894. 1994X    4154
  184895. 4161Y
  184896. 13229
  184897. OVERMAN, L. E.
  184898. JOCCBALLYLSILANES EQUIVALENT STANNANES CHEMISTRY ALLENES SILICON ALPHA M
  184899. 14238N
  184900. 2/28/96
  184901. A_REGIOSELECTIVE OPENING OF TERMINAL EPOXIDES WITH 2
  184902. (TRIALKYLSILYL)ALLYL ORGANOMETALLIC REAGENTS
  184903. 1994X    4138
  184904. 4142Y
  184905. 13230
  184906. A    CHINI, M.
  184907. (BENZYLOXY)CYCLOHEXENE M
  184908. 14239N
  184909. 2/28/96
  184910. REGIOCHEMICAL CONTROL OF THE RING OPENING OF 1,2
  184911. EPOXIDES BY MEANS OF CHELATING PROCESSES .7. SYNTHESIS AND RING
  184912. OPENING REACTIONS OF CIS
  184913.  AND TRANS
  184914. OXIDES DERIVED FROM 2
  184915. (BENZYLOXY)
  184916. DIHYDRO
  184917. PYRAN
  184918. 1994 X    4131
  184919. 4137Y
  184920. 13231
  184921. BACKVALL, J. E.
  184922. ORGANOCOPP ER REAGENTS LEAVING GROUP DERIVATIVES ALKYLATION STEREOCHEMISTRY CARBOXYLATES SN2' REGIOCHEMISTRY SELECTIVITY ALLYLATION M
  184923. 14240N
  184924. 2/28/96
  184925. A`REGIOCONTROL IN COPPER
  184926. CATALYZED CROSS COUPLING OF ALLYLIC CHLORIDES WITH ARYL GRIGNARD REAGENTS
  184927. 1994X    4126
  184928. 4130Y
  184929. 13232
  184930. FITZGERALD, J. J.
  184931. JOCC@ANTIFUNGAL ISOCOUMARINS HYDRANGENOL DERIVATIVES EFFICIENT TASTE M
  184932. 14241N
  184933. 2/28/96
  184934. AlREACTION OF BENZOCYCLOBUTENOXIDES WITH ALDEHYDES: SYNTHESIS OF PESHAWARINE AND OTHER 3,4
  184935. DIHYDROISOCOUMARINS
  184936. 1994X    4117
  184937. 4121Y
  184938. 13233
  184939. RANU, B. C.
  184940. HIGHLY SELECTIVE REDUCTION SILICA
  184941. GEL SODIUM
  184942. BOROHYDRIDE CONJUGATED NITROALKENES EFFICIENT REDUCTION 2,3
  184943. EPOXY ALCOHOLS AROYL AZIDES AMINES ALDEHYDES CLEAVAGE M
  184944. 14242N
  184945. 2/28/96
  184946. A)REDUCTION OF AZIDES WITH ZINC BOROHYDRIDE
  184947. 1994 X    4114
  184948. 4116Y
  184949. 13234
  184950. FUJIMURA, O.
  184951. GRUBBS B
  184952. CARBENE COMPLEX POLYMERIZATION DIENES 
  184953. CYCLIC VINYL ETHER CATALYST MOLYBDENUM 2+2 METATHESIS HETEROCYCLE INTRAMOLECULAR CATALYTICM
  184954. 14243N
  184955. 2/28/96
  184956. A_THE SYNTHESIS OF CYCLIC ENOL ETHERS VIA MOLYBDENUM ALKYLIDENE
  184957. CATALYZED RING
  184958. CLOSING METATHESIS
  184959. 1994 X    4029
  184960. 4031Y
  184961. 13235
  184962. Cho, I. S. B
  184963. JOCC8ASPARTIC ACID ANTAGONISTS CRYSTAL
  184964. STRUCTURE EXPLORATION M
  184965. 14244N
  184966. 2/28/96
  184967. ANPALLADIUM CATALYZED HYDROGENATION OF A,b
  184968. UNSATURATED SULFONES AND PHOSPHONATES
  184969. 1994 X    4027
  184970. 4028Y
  184971. 13236
  184972. SEMMELHACK, M. F.
  184973. JACSM
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  184975. 2/28/96
  184976. PALLADIUM
  184977. PROMOTED SYNTHESIS OF IONOPHORE ANTIBIOTICS. STRATEGY AND ASSEMBLY OF THE HOMOCHIRAL TETRAHYDROFURAN AND TETRAHYDROPYRAN PORTIONS OF TETRONOMYCIN
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  184979. 7456Y
  184980. 13237
  184981. GILBERT, A. M.
  184982. JACSM
  184983. 14246N
  184984. 2/28/96
  184985. ASPALLADIUM
  184986. CATALYZED CROSS
  184987. COUPLING OF ARENE
  184988. CHROMIUM TRICARBONYL TRIFLATE COMPLEXES
  184989. 1994 X    7449
  184990. 7450Y
  184991. 13238
  184992. STURINO, C. F.
  184993. FALLIS B
  184994. JACSCgRADICAL HYDRAZONE AMINO CYCLIZATION SAMARIUM IODIDE HETEROATOM RADICAL CLOCK HYDRAZONE CONVERSION AMINEM
  184995. 14247N
  184996. 2/28/96
  184997. APSAMARIUM(II) IODIDE INDUCED RADICAL CYCLIZATIONS OF HALO
  184998.  AND CARBONYLHYDRAZONES
  184999. 1994 X    7447
  185000. 7448Y
  185001. 13239
  185002. KUPFER, R.
  185003. JACSC
  185004. PHOTOCHEMICAL REACTIVITY PHOTOGENERATED REAGENTS BETA
  185005. CYCLODEXTRIN CYCLOMALTOHEPTAOSE ADAMANTANYLIDENE ADAMANTYLIDENE COMPLEXES MIGRATION CATALYSTS MEMBRANE M
  185006. 14248N
  185007. 2/28/96
  185008. CARBENE REARRANGEMENTS .43. CARBENE REARRANGEMENTS IN CONSTRAINED SYSTEMS .2. CARBENES IN CONSTRAINED SYSTEMS .2. FIRST CARBENE REACTIONS WITHIN ZEOLITES 
  185009.  SOLID STATE PHOTOLYSIS OF ADAMANTANE
  185010. SPIRO
  185011. DIAZIRINE
  185012. 1994 X    7393
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  185014. 13240
  185015. SEMMELHACK, M. F.
  185016. JACSCVREGIOSPECIFIC SYNTHESIS ORGANIC
  185017. SYNTHESIS CYCLOADDITION DOTZ REACTION ALKYNES LIGANDS M
  185018. 14249N
  185019. 2/28/96
  185020. METAL
  185021. CATALYZED CYCLOPROPENE REARRANGEMENTS FOR BENZANNULATION: EVALUATION OF AN ANTHRAQUINONE SYNTHESIS PATHWAY AND REEVALUATION OF THE PARALLEL APPROACH VIA CARBENE
  185022. CHROMIUM COMPLEXES
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  185025. 13241
  185026. ADAM, W.
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  185028. ELECTRON
  185029. RESONANCE AZO
  185030. BRIDGES N=N
  185031. BONDS PARALLEL C=C 2+2 PHOTOCYCLOADDITION RELUCTANT AZOALKANES DEFICIENT DIENES PHOTOCHEMISTRY AZINES BIRADICALS M
  185032. 14250N
  185033. 2/28/96
  185034. TEMPERATURE DEPENDENCE OF THE a VERSUS b BOND CLEAVAGE IN THE DIRECT AND TRIPLET
  185035. SENSITIZED PHOTOLYSIS OF AZOALKANES OF THE 2,3
  185036. DIAZABICYCLO[2.2.1]HEPT
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  185041. DENMARK, S. E.
  185042. SILYL ENOL ETHERS INDUCED RING ENLARGEMENT HIGH
  185043. PRESSURE REACTION LEWIS ACID KETENE ACETALS NEUTRAL CONDITIONS STEREOCHEMICAL CONTROL CLAISEN REARRANGEMENT CARBONYL
  185044. COMPOUNDS ORGANIC
  185045. SYNTHESIS 
  185046. DIRECTED FELKIN
  185047. ANH CRAM SILICON SILYL CATALYST TRANSITION STATE
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  185049. 2/28/96
  185050. APCHEMISTRY OF ENOXYSILACYCLOBUTANES: HIGHLY SELECTIVE UNCATALYZED ALDOL ADDITIONS
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  185054. CRISTAU, H. J.
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  185058. A6SYNTHETIC APPLICATIONS OF METALATED PHOSPHONIUM YLIDES
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  185062. KITANO, K.
  185063. Chem. Lett.C$DIELS
  185064. ALDER NUCLEOSIDES DERIVATIVES M
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  185066. 2/28/96
  185067. DIMETHYL 2
  185068. BIS(METHOXYCARBONYL)BICYCLO[2.2.1]HEPT
  185069. YL}MALONATE. SYNTHESIS AND BASE
  185070. CATALYZED C
  185071. C BOND CLEAVAGE REACTION
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  185075. YANADA, R.
  185076. Chem. Lett.C
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  185081. AFREDUCTION WITH SAMARIUM(0). DEBROMINATION OF VIC
  185082. DIBROMIDES TO ALKENES
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  185086. NAGATA, T.
  185087. Chem. Lett.
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  185090. 2/28/96
  185091. ENANTIOSELECTIVE AEROBIC EPOXIDATION OF ACYCLIC SIMPLE OLEFINS CATALYZED BY THE OPTICALLY ACTIVE b
  185092. KETOIMINATO MANGANESE(III) COMPLEX
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  185101. INTRODUCTION OF DIFFERENT GROUPS TO A
  185102.  AND b
  185103. POSITIONS OF CYCLIC A,b
  185104. UNSATURATED KETONES VIA [2p + 2p] PHOTOCYCLOADDITION WITH KETENE SILYL ACETALS FOLLOWED BY ELECTRODE REACTION
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  185108. MATSUMOTO, K.
  185109. Chem. Lett.C
  185110. CLEAVAGE BOND M
  185111. 14257N
  185112. 2/28/96
  185113. ARTHE USE OF A
  185114. TRIMETHYLSILYL
  185115. UNSATURATED KETONES AS 1
  185116. ACYLETHENYL ANION SYNTHON
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  185124. 2/28/96
  185125. AMPHOTOCHEMICAL ELECTRON TRANSFER REACTIONS 
  185126.  APPLICATIONS TO ORGANIC SYNTHESIS
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  185128. U606Y
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  185130. Gil, R.B
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  185132. PALLADIUM CATALYSIS ALLYLIC ALKYLATION AXIAL CHIRALITY ENANTIOSELECTIVITY ALKYLIDENE CYCLOBUTANE CHIRAL LITHIUM AMIDES ENANTIOSELECTIVE DEHYDROHALOGENATION VERSATILE SYNTHESIS KINETIC RESOLUTION M
  185133. 14259N
  185134. 2/28/96
  185135. AoSELECTIVITIES IN THE PALLADIUM
  185136. CATALYZED SYNTHESIS OF DIMETHYL [2
  185137. SUBSTITUTED CYCLOBUTYLIDENE)ETHYL]MALONATE
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  185141. Bull. Soc. Chim. Fr.C
  185142. ALLYLIC HALIDES ALPHA
  185143. HALOCARBANIONS ALLYLSILANES ALLYLTIN DERIVATIVES ALPHA
  185144. CHLOROHYDRINS VINYLEPOXIDES DIASTEREO
  185145. SELECTIVITY STEREOSELECTIVE SYNTHESIS GEM
  185146. DICHLOROALLYLLITHIUM HALOALLYLBORONATE ESTER M
  185147. 14260N
  185148. 2/28/96
  185149. AmREACTIONS OF A
  185150. HALOALLYLLITHIUM DERIVATIVES WITH CARBON, SILICON, TIN OR BORON HALIDES AND CARBONYL COMPOUNDS
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  185153. PRAGER, R. H. 
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  185155. ETHOXYMETHYLENEMALONATE M
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  185158. AbHETEROCYCLIC SYNTHESIS WITH AZIDES .3. REACTIONS OF TRIAZOLINES MADE FROM ARYLMETHYLIDENEMALONATES
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  185161. 13253
  185162. PRAGER, R. H. 
  185163. Aust. J. Chem.CANITROGEN
  185164. BRIDGEHEAD COMPOUNDS PYRROLO<1,2
  185165. A>QUINOLINE
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  185168. 2/28/96
  185169. A[THE CHEMISTRY OF 5
  185170. OXODIHYDROISOXAZOLES .9. ANNELATED PYRIMIDINES BY FLASH VACUUM PYROLYSIS
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  185173. 13254
  185174. PRAGER, R. H. 
  185175. Aust. J. Chem.C
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  185179. A]THE CHEMISTRY OF 5
  185180. OXODIHYDROISOXAZOLES .8. PHOTOLYSIS OF 2
  185181. (HETEROCYCLYL)ISOXAZOL
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  185184. 1262Y
  185185. 13255
  185186. KOLDOBSKII, G.
  185187. Acta Chem. Scand.M
  185188. 14264N
  185189. 2/28/96
  185190. A\SYNTHESIS OF 3H
  185191. 1,3,4
  185192. BENZOTRIAZEPINES FROM 5
  185193. ARYLTETRAZOLES AND N
  185194. ARYLBENZIMIDOYL CHLORIDES
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  185197. BJORSVIK, H. R.
  185198. Acta Chem. Scand.C
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  185202. AN OBSERVATION OF CATIONIC INFLUENCE ON THE N/O ALKYLATION SELECTIVITY IN THE ALKYLATION OF A COMPOUND CONTAINING SEVERAL NUCLEOPHILIC SITES
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  185205. KUMARAN, G.
  185206. Tet. Lett.C
  185207. CYCLOADDITION K
  185208. HYDROXIMOYL CHLORIDES BEARING ALPHA
  185209. CHLORO FUNCTIONALITY WERE PREPARED FROM CONJUGATED NITRO OLEFINS USING TICL4 AT ROOM TEMPERATURE IN MODERATE TO GOOD YIELDS.M
  185210. 14266N
  185211. 2/28/96
  185212. AhA FACILE CONVERSION OF NITRO OLEFINS TO FUNCTIONALISED HYDROXIMOYL CHLORIDES AS NITRILE OXIDE PRECURSORS
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  185217. Tet. Lett.C=BETA
  185218. FRAGMENTATION INTRAMOLECULAR FUNCTIONALIZATION REAGENTS 
  185219. THE STEROIDAL 5 ALPHA
  185220. ALCOHOL (3) WITH (DIACETOXYIODO)
  185221. BENZENE AND IODINE UNDER IRRADIATION WITH VISIBLE LIGHT UNDERGOES A TANDEM ALKOXY RADICAL BETA
  185222. FRAGMENTATION 
  185223. CYCLOPROPYLCARBINYL REARRANGEMENT REACTION TO GIVE THE ELEVEN
  185224. MEMBERED CYCLIC KETONE (4). UNDER OXYGEN PRESSURE PEROXIDATION OF THE C
  185225. RADICAL INTERMEDIATE RAKES PLACE TO AFFORD THE HIGHLY FUNCTIONALIZED ELEVEN
  185226. MEMBERED CYCLIC KETONE (6) IN MODERATE YIELD.
  185227. 14267N
  185228. 2/28/96
  185229. SEQUENTIAL ALKOXY RADICAL FRAGMENTATION
  185230. CYCLOPROPYLCARBINYL REARRANGEMENT. SYNTHESIS OF HIGHLY FUNCTIONALIZED ELEVEN
  185231. MEMBERED RINGS
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  185234. 13259
  185235. HUNTER, R.
  185236. Tet. Lett.C
  185237. EQUIVALENTS ACETALS ENONES 
  185238. GAMMA
  185239. HETEROSUBSTITUTED VINYLTHIONIUM IONS REGIOSELECTIVELY AND DIASTEREOSELECTIVELY ALLYLATE ENOL SILYL ETHERS. INTRAMOLECULAR CAPTURE OF A VINYLTHIONIUM ION IS USED AS A KEY STEP OF A NOVEL PENTANNULATION SEQUENCE.M
  185240. 14268N
  185241. 2/28/96
  185242. AZREGIOSELECTIVE ALLYLATION OF ENOL SILYL ETHERS WITH g
  185243. HETEROSUBSTITUTED VINYLTHIONIUM IONS
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  185245. 5484Y
  185246. 13260
  185247. BADONE, D.
  185248. Tet. Lett.C
  185249. ALLENES IODIDES K
  185250. THE PALLADIUM
  185251. COPP ER CO
  185252. CATALYZED CROSS
  185253. COUPLING REACTION OF N
  185254. TRIBUTYLALLENYL STANNANE 1 WITH ARYL TRIFLATES PROVIDES AN EFFICIENT ROUTE TO THE CORRESPONDING ARYL ALLENES.M
  185255. 14269N
  185256. 2/28/96
  185257. AnTHE STILLE COUPLING REACTION OF ARYL TRIFLATES WITH N
  185258. TRIBUTYLALLENYL STANNANE: A GENERAL ROUTE TO ARYLALLENES
  185259. 1994 X    5477
  185260. 5480Y
  185261. 13261
  185262. ALCARAZ, L.
  185263. Tet. Lett.K
  185264. CARBON HOMOLOGATION OF BENZYLIC, ALLYLIC, PROPARGYLIC AND PRIMARY HALIDES OR MESYLATES WITH DIMETHYLSULFONIUM METHYLIDE AFFORDS TERMINAL OLEFINS IN GOOD TO EXCELLENT YIELDS.M
  185265. 14270N
  185266. 2/28/96
  185267. A0SULFUR YLIDE VINYLATION OF HALIDES AND MESYLATES
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  185269. 5456Y
  185270. 13262
  185271. ALCARAZ, L.
  185272. Tet. Lett.C    OXETANES 
  185273. THE REACTION OF EXCESS OF DIMETHYLSULFONIUM METHYLIDE WITH TERMINAL, ALLYLIC, OR BENZYLIC EPOXIDES AFFORDS GOOD TO EXCELLENT YIELDS OF ONE CARBON HOMOLOGATED ALLYLIC ALCOHOLS.M
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  185276. AfNOVEL CONVERSION OF EPOXIDES TO ONE CARBON HOMOLOGATED ALLYLIC ALCOHOLS BY DIMETHYLSULFONIUM METHYLIDE
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  185280. HECK, M. P.
  185281. Tet. Lett.C#IODOTRIMETHYLSILANE SUGAR LACTONES K
  185282. THE REACTION OF IODOTRIMETHYLSILANE WITH SUGAR LACTONES PROTECTED BY ESTER GROUPS LEADS TO PRIMARY IODIDES OF THE SAME CONFIGURATION.M
  185283. 14272N
  185284. 2/28/96
  185285. AMUNEXPECTED OUTCOME IN THE REACTION OF SUGAR LACTONES WITH IODOTRIMETHYLSILANE
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  185289. CHANDRASEKHAR, S.
  185290. Tet. Lett.C
  185291. HYDROXYPHENYLSULFONE DESULFONYLATION ALKYLATION DIIODOSAMARIUM OLEFIN SYNTHESIS SULFONES DERIVATIVES ALKYLATION DIIODIDE HALIDES K
  185292. SMI2 MEDIATES THE IN SITU REDUCTIVE ADDITION OF GEMINAL BIS
  185293. PHENYLSULFONES TO UNHINDERED KETONES AT ROOM TEMPERATURE AFFORDING BETA
  185294. HYDROXYPHENYLSULFONES IN GOOD TO EXCELLENT YIELDS.M
  185295. 14273N
  185296. 2/28/96
  185297. AASMI2 MEDIATED REDUCTIVE ADDITION OF BIS
  185298. PHENYLSULFONES TO KETONES
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  185303. FALCK B
  185304. Tet. Lett.
  185305. DESULFONYLATION LITHIUM NAPHTHALENIDE ALKYLATION ALPHA
  185306. SULFONYL CARBANION SULFONES 
  185307. BIS SULFONE REDUCTIVE REDUCTION CARBANION ALKYLATION LITHIUM NAPTHALENIDE SULFONYL DESULFONYLATIONK
  185308. REDUCTIVE CLEAVAGE OF GEMINAL BIS
  185309. PHENYLSULFONES USING LITHIUM NAPHTHALENIDE IN THF AT 
  185310. 78 DEGREES C SELECTIVELY AFFORDS ALPHA
  185311. SULFONYL CARBANIONS WHICH PARTICIPATE IN TYPICAL REACTION WITH ELECTROPHILES.M
  185312. 14274N
  185313. 2/28/96
  185314. A*REDUCTIVE LITHIATION OF BIS
  185315. PHENYLSULFONES
  185316. 1994 X    5437
  185317. 5440Y
  185318. 13266
  185319. SHAPIRO, G.
  185320. Tet. Lett.CISOLID
  185321. PHASE SYNTHESIS PEPTIDE
  185322. SYNTHESIS DEPROTECTION PHOSPHATE FRAGMENTS 
  185323. UNDER PALLADIUM CATALYSIS VARIOUS ALLYLESTER PROTECTING GROUPS ARE RAPIDLY CLEAVED IN HIGH YIELD WITH THE REAGENT 8:3 TRIMETHYLSILYLAZIDE/TETRABUTYLAMMONIUM FLUORIDE. THE EFFICIENCY OF THIS METHOD MAKES IT PARTICULARLY USEFUL FOR SOLID PHASE DEPROTECTIONS.
  185324. 14275N
  185325. 2/28/96
  185326. AaMILD AND RAPID AZIDE
  185327. MEDIATED, PALLADIUM CATALYZED CLEAVAGE OF ALLYLESTER BASED PROTECTING GROUPS
  185328. 1994 X    5421
  185329. 5424Y
  185330. 13267
  185331. CURRAN, T. P.
  185332. Tet. Lett.C
  185333. REDUCED PEPTIDE
  185334. BOND SOLID
  185335. PHASE SYNTHESIS ANALOGS BACKBONE POTENT AMIDE INHIBITORS PROTEASE ISOSTERE RENIN 
  185336. BOC PROTECTION AMINE GROUP DEPROTECTION ACIDIC BASIC CONDITIONS SELECTIVE MECHANISM
  185337. REACTION OF 3, THE N
  185338. BOC, O
  185339. TOSYL DERIVATIVE OF PHENYLALANINOL, WITH BASE LEADS TO LOSS OF THE BOC AND TOSYL GROUPS AND FORMATION OF OXAZOLIDINONE 9. SIMILAR REACTIONS HAVE ALSO BEEN EXAMINED. A MECHANISM TO EXPLAIN LOSS OF THE BOC GROUP UNDER BASIC REACTION CONDITIONS IS PROPOSED.
  185340. 14276N
  185341. 2/28/96
  185342. AOLOSS OF THE TERT
  185343. BUTYLOXYCARBONYL (BOC) PROTECTING GROUP UNDER BASIC CONDITIONS
  185344. 1994 X    5409
  185345. 5412Y
  185346. 13268
  185347. HANESSIAN, S.
  185348. Tet. Lett.
  185349. WHEN NEARED WITH A REAGENT PREPARED FROM EQUIMOLAR QUANTITIES OF METHYLLITHIUM AND COPPER IODIDE, 7,21
  185350. TMS BAFILOMYCIN A(2) 3 UNDERGOES RING EXPANSION TO GIVE THE 18
  185351. MEMBERED LACTONE HOMOLOG 5 IN NEARLY QUANTITATIVE YIELD. ACID HYDROLYSIS GIVES ISO
  185352. BAFILOMYCIN A(1). RING CONTRACTION TO THE ORIGINAL 16
  185353. MEMBERED LACTONE TAKES PLACE IN THE PRESENCE OF FLUORIDE ION. A MECHANISTIC RATIONALE AND X
  185354. RAY CRYSTALLOGRAPHIC EVIDENCE ARE PRESENTED.
  185355. 14277N
  185356. 2/28/96
  185357. A[AN UNPRECEDENTED RING EXPANSION IN THE MACROLIDE SERIES 
  185358.  SYNTHESIS OF ISO
  185359. BAFILOMYCIN A(1)
  185360. 1994 X    5393
  185361. 5396Y
  185362. 13269
  185363. JEONG, J. U.
  185364. Tet. Lett.
  185365. CATALYZED EQUILIBRATION OF SPIROKETALS 55H BETA BETA AND 55H ALPHA BETA INVOLVES A TWO STAGE PROCESS WHEREBY THE 1,6
  185366. DIOXASPIRO[4.4]NONANES CAN BE EQUILIBRATED UNDER MILD CONDITIONS TO A PAIR OF 1,6
  185367. DIOXASPIRO[4.5]DECANES WITH PRESERVATION OF THE ADJACENT C
  185368. 20 METHYL STEREOCENTER. UNDER MORE FORCING CONDITIONS, BOTH CENTERS CAN BE EQUILIBRATED IN A REACTION INVOLVING VINYL ETHETER INTERMEDIATE 10H.
  185369. 14278N
  185370. 2/28/96
  185371. SPIROKETAL EQUILIBRATION: INTERCONVERSION OF 1,6
  185372. DIOXASPIRO[4.4]NONANES AND 1,6
  185373. DIOXASPIRO[4.5]DECANES. IMPLICATIONS FOR THE SYNTHESIS OF CEPHALOSTATIN
  185374. 1994X    5385
  185375. 5388Y
  185376. 13270
  185377. DERBESY, G.
  185378. Tet. Lett.C
  185379. SULFUR CHEMISTRY ALLIUM K
  185380. UNSYMMETRICAL DI
  185381.  AND TETRASULFIDES CAN BE PREPARED IN A ONE
  185382. POT REACTION USING SO2CL2, SCL2 AND S2CL2 RESPECTIVELY TO PERMIT COUPLING OF THE APP ROPRIATE THIOLS.M
  185383. 14279N
  185384. 2/28/96
  185385. ADA SIMPLE METHOD TO PREPARE UNSYMMETRICAL DI
  185386. , TRI
  185387.  AND TETRASULFIDES
  185388. 1994 X    5381
  185389. 5384Y
  185390. 13271
  185391. COREY, E. J.
  185392. Tet. Lett.KuAN EFFICIENT CATALYTIC ENANTIOSELECTIVE SYNTHESIS OF THE IMPORTANT ANTIDEPRESSANT SERTRALINE IS DESCRIBED (SCHEME I).M
  185393. 14280N
  185394. 2/28/96
  185395. AWA CATALYTIC ENANTIOSELECTIVE SYNTHETIC ROUTE TO THE IMPORTANT ANTIDEPRESSANT SERTRALINE
  185396. 1994 X    5373
  185397. 5376Y
  185398. 13272
  185399. NIEMAN, J. A. 
  185400. KEAY B
  185401. Tet. Lett.CLLITHIUM EQUIVALENTS BASICITY 
  185402. FURAN SILYL SILICON DESILYLATION 2,4
  185403.  FLUORIDE
  185404. STREATMENT OF 2
  185405. (TERT
  185406. BUTYLDIMETHYLSILYL)
  185407. (TRIETHYLSILYLOXYMETHYL)FURAN WITH 1.3 EQUIV. OF N
  185408. BULI (THF, 
  185409. 40 DEGREES, 3H), FOLLOWED BY THE ADDITION OF A VARIETY OF ELECTROPHILES PROVIDED 2,3,5
  185410. TRISUBSTITUTED FURANS, WHICH UPON TREATMENT WITH TETRA
  185411. BUTYLAMMONIUM FLUORIDE AFFORDED 2,4
  185412. DISUBSTITUTED FURANS IN MODERATE TO EXCELLENT YIELDS.
  185413. 14281N
  185414. 2/28/96
  185415. A0A FACILE PREPARATION OF 2,4
  185416. DISUBSTITUTED FURANS
  185417. 1994 X    5335
  185418. 5338Y
  185419. 13273
  185420. COMINS, D. L.
  185421. Tet. Lett.C'ALPHA
  185422. AMINO ALKOXIDES ORTHO
  185423. LITHIATION 
  185424. DE RING CAMPTOTHECIN INTERMEDIATE II WAR PREPARED ENANTIOSELECTIVELY FROM 2
  185425. CHLORO
  185426. 6 HYDROXYPYRIDINE IN SIX STEPS AND USED IN A NINE
  185427. STEP SYNTHESIS OF (S)
  185428. CAMPTOTHECIN.M
  185429. 14282N
  185430. 2/28/96
  185431. AYASYMMETRIC SYNTHESIS OF CAMPTOTHECIN ALKALOIDS: A NINE
  185432. STEP SYNTHESIS OF (S)
  185433. CAMPTOTHECIN
  185434. 1994  X    5331
  185435. 5334Y
  185436. 13274
  185437. REETZ, M. T.
  185438. B    SynthesisC
  185439. CHIRAL ALPHA
  185440. ALKOXY PI
  185441. FACIAL DIASTEREOSELECTIVITY NON
  185442. CHELATION
  185443. CONTROL NUCLEOPHILIC ADDITIONS CARBONYL
  185444. COMPOUNDS DIPEPTIDE ISOSTERES ORGANIC
  185445. SYNTHESIS 2
  185446. AMINO ALCOHOLS ALDEHYDES ESTERS M
  185447. 14283N
  185448. 2/28/96
  185449. ABSTEREOSELECTIVE SYNTHESIS OF A,b
  185450. DIAMINO NITRILES FROM AMINO ACIDS
  185451. 1994X
  185452. 13275
  185453. BEW, S. P.
  185454. B    SynthesisC
  185455. SULFOLENES M
  185456. 14284N
  185457. 2/28/96
  185458. A?SYNTHESIS OF A STABLE 2
  185459. TRIBUTYLSTANNYL
  185460. BUTADIENE PRECURSOR
  185461. 1994 X
  185462. 13276
  185463. DEKIMPE, N.
  185464. B    SynthesisM
  185465. 14285N
  185466. 2/28/96
  185467. ADREGIOSPECIFIC SYNTHESIS OF A
  185468. AMINO KETO ACETALS (b,b
  185469. DIALKOXYAMINES)
  185470. 1994 X
  185471. 13277
  185472. KITAHARA, T.
  185473. B    SynthesisC
  185474. SCLEROSPORIN ENANTIOMERS M
  185475. 14286N
  185476. 2/28/96
  185477. A=FACILE PREPARATION OF CONJUGATED DIENES FROM ALLYLIC ALCOHOLS
  185478. 1994 X
  185479. 13278
  185480. SAIKIA, A. K.
  185481. B    SynthesisC+ORGANIC
  185482. SYNTHESIS NITROALKENES DEHYDRATION M
  185483. 14287N
  185484. 2/28/96
  185485. A0AN IMPROVED SYNTHESIS OF CONJUGATED NITROOLEFINS
  185486. 1994X
  185487. 13279
  185488. A    ROLFS, A.
  185489. B    SynthesisM
  185490. 14288N
  185491. 2/28/96
  185492. ASEFFICIENT SYNTHESIS OF 3
  185493. AMINOTHIOACRYLAMIDES BY IMINOFORMYLATION OF THIOACETAMIDES
  185494. 1994X
  185495. 13280
  185496. A    LI, W. D.
  185497. B    SynthesisM
  185498. 14289N
  185499. 2/28/96
  185500. AUA FACILE TOTAL SYNTHESIS OF (+/
  185501. CEMBRENE BY TITANIUM
  185502. INDUCED KETO ESTER CYCLIZATION
  185503. 1994 X
  185504. 13281
  185505. MITCHELL, M. A.
  185506. B    SynthesisC9OXAZOLINES DELTA
  185507. THIAZOLINES DELTA
  185508. OXAZOLINES AMIDES M
  185509. 14290N
  185510. 2/28/96
  185511. AVSYNTHESIS OF d2
  185512. OXAZOLINES AND d2
  185513. OXAZINES USING POTASSIUM FLUORIDE ON ALUMINA
  185514. 1994X
  185515. 13282
  185516. DALPIAZ, V.
  185517. B    SynthesisC
  185518. SYNTHETIC APP ROACH SYSTEM M
  185519. 14291N
  185520. 2/28/96
  185521. ACETYL
  185522. METHYL
  185523. NITRO
  185524. PHENYL
  185525. 3(2H)
  185526. PYRIDAZINONE: VERSATILE PRECURSOR TO HETERO
  185527. CONDENSED PYRIDAZINONES
  185528. 1994 X
  185529. 13283
  185530. CRISP, G. T.
  185531. B    SynthesisM
  185532. 14292N
  185533. 2/28/96
  185534. AASYNTHESIS OF FUNCTIONALISED VINYL TRIFLATES FROM TERMINAL ALKYNES
  185535. 1994 X
  185536. 13284
  185537. LEY, S. V.
  185538. B    Synthesis
  185539. ENANTIOSELECTIVE TOTAL SYNTHESIS ANTIBIOTIC CP
  185540. 61,405 ROUTIENNOCIN PHOSPHORUS
  185541.  CONTAINING INHIBITORS TRANSITION
  185542. METAL OXO HMG
  185543. COA REDUCTASE DIELS
  185544. ALDER ROUTE CLAISEN REARRANGEMENT CHIRAL LACTONES BUILDING
  185545. BLOCKS MESO DIOLS M
  185546. 14293N
  185547. 2/28/96
  185548. A]TETRAPROPYLAMMONIUM PERRUTHENATE, PR4N+RUO4
  185549. , TPAP: A CATALYTIC OXIDANT FOR ORGANIC SYNTHESIS
  185550. 1994 X
  185551. 13285
  185552. WELLMAKER, G. S.
  185553. Org. Prep. Proc. Int.K
  185554. (VOL 25, PG 595, 1993)M
  185555. 14294N
  185556. 2/28/96
  185557. AJA SIMPLE, EFFICIENT PREPARATION OF 1,1
  185558. BIS(TRIMETHYLSILOXY)
  185559. BUTADIENE 
  185560. 1994 X
  185561. 13286
  185562. ATTANASI, O. A.
  185563. Org. Prep. Proc. Int.M
  185564. 14295N
  185565. 2/28/96
  185566. AuTREATMENT OF CONJUGATED AZOALKENES WITH N
  185567. TOSYLHYDRAZADINES 
  185568.  A USEFUL ENTRY TO ASYMMETRIC BIS
  185569. ACYLHYDRAZONES
  185570. 1994 X
  185571. 13287
  185572. BARBRY, D.
  185573. Org. Prep. Proc. Int.M
  185574. 14296N
  185575. 2/28/96
  185576. A>IMPROVED ALKYLATION OF ETHYL ACETOACETATE AND DIETHYL MALONATE
  185577. 1994X
  185578. 13288
  185579. ELGEMEIE, G. E. H.
  185580. Org. Prep. Proc. Int.M
  185581. 14297N
  185582. 2/28/96
  185583. A4SYNTHESIS OF SEVERAL N
  185584. SUBSTITUTED AMINO
  185585. PYRIDONES
  185586. 1994 X
  185587. 13289
  185588. CHA, J. S.
  185589. Org. Prep. Proc. Int.M
  185590. 14298N
  185591. 2/28/96
  185592. AQREDUCTION OF ORGANIC COMPOUNDS WITH SODIUM ALUMINUM HYDRIDE IN THEORETICAL AMOUNT
  185593. 1994X
  185594. 13290
  185595. KATRITZKY, A. R.
  185596. Org. Prep. Proc. Int.M
  185597. 14299N
  185598. 2/28/96
  185599. A^AN ALTERNATIVE SYNTHESIS OF ARYL AND HETEROARYL BROMIDES FROM ACTIVATED ARYL HYDROXY COMPOUNDS
  185600. 1994X
  185601. 13291
  185602. OHWADA, T.
  185603. FACES CARBONYL GROUPS OLEFIN GROUPS PI
  185604. INTERACTIONS UNSYMMETRIZATION OF PI
  185605. LOBES DIELS
  185606. ALDER REACTION FACIAL STEREOSELECTIVITY REMOTE SUBSTITUENTS OSMIUM TETRAOXIDE CYCLOADDITIONS M
  185607. 14300N
  185608. 2/28/96
  185609. AuORBITALS DISTORTION OF CARBONYL AND OLEFIN GROUPS 
  185610.  UNSYMMETRIZATION OF p
  185611. LOBES ARISING FROM p
  185612. ORBITAL INTERACTIONS
  185613. 1994X
  185614. 13292
  185615. WARSINSKY, R.
  185616. J.C.S. Perkin Trans. 1
  185617. aCUASYMMETRIC INDUCTION METAL
  185618. SALTS CYCLIZATIONS ESTERS NITROALKANES PRECURSORS SYSTEMS M
  185619. 14301N
  185620. 2/28/96
  185621. OXIDATIVE FREE
  185622. RADICAL ADDITIONS OF A-NITRO KETONES AND A
  185623. NITRO AMIDES TO ALKENES AND ALKYNES MEDIATED BY ELECTROCHEMICALLY REGENERABLE MANGANESE(III) ACETATE
  185624. 1994 X    2027
  185625. 2037Z
  185626. 13293
  185627. AITKEN, R. A.
  185628. DIOXIDE M
  185629. 14302N
  185630. 2/28/96
  185631. PREPARATION AND PYROLYSIS OF SOME BI
  185632.  AND TRI
  185633. CYCLIC SULFONES DERIVED FROM PHOTOCHEMICAL [2+2] CYCLOADDITION OF 2,3
  185634. DIHYDROTHIOPHENE-1,1
  185635. DIOXIDE (2
  185636. SULFOLENE)
  185637. 13294
  185638. HIGUCHI, H.
  185639. J.C.S. Perkin Trans. 1C
  185640. D2SO4M
  185641. 14303N
  185642. 2/28/96
  185643. AoSYNTHESIS AND PROPERTIES OF TETRAMETHYLOCTADEHYDRODIHYDRO
  185644. [C26]
  185645.  AND [34]
  185646. ANNULENEDIONES
  185647. 1994 X    1957
  185648. 1968Z
  185649. 13295
  185650. PARSONS, A. F.
  185651. J.C.S. Perkin Trans. 1C
  185652. COBALT
  185653. MEDIATED CYCLIZATION ENANTIOSELECTIVE SYNTHESIS CLITOCYBE
  185654. ACROMELALGA (
  185655. ALPHA
  185656. KAINIC ACID 5
  185657. MEMBERED LACTAMS FORMAL SYNTHESIS DERIVATIVES TEMPERATURE AMIDES ROUTE M
  185658. 14304N
  185659. 2/28/96
  185660. A`SYNTHESIS OF PYRROLIDINONES VIA FREE
  185661. RADICAL CYCLISATIONS: POTENTIAL APPLICATION TO THE KAINOIDS
  185662. 1994 X    1945
  185663. 1951Z
  185664. 13296
  185665. BRYCE, M. R.
  185666. J.C.S. Perkin Trans. 1CwSPECTROSCOPIC DETECTION ADDITIONS ARN=S N
  185667. (ARYLAMINOTHIO)PHTHALIMIDES HETERODIENOPHILES FRAGMENTATION CHEMISTRY DIENES M
  185668. 14305N
  185669. 2/28/96
  185670. DIELS
  185671. ALDER AND ENE REACTIONS OF NEW TRANSIENT THIONITROSOARENES (AR
  185672. N=S) AND THIONITROSOHETEROARENES (HET
  185673. N=S) GENERATED FROM N
  185674. (ARYLAMINOSULFANYL) AND N
  185675. (HETEROARYLAMINOSULFANYL)
  185676. PHTHALIMIDES: SYNTHESIS OF CYCLIC AND ACYCLIC SULFENAMIDES
  185677. 1994X    1935
  185678. 1944Z
  185679. 13297
  185680. KITAMURA, T.
  185681. J.C.S. Perkin Trans. 1C    BROMIDES M
  185682. 14306N
  185683. 2/28/96
  185684. A}INTRAMOLECULAR CYCLIZATION TO 1
  185685. PHENYL
  185686. BENZOTHIOPHENIUM SALTS BY ELECTROPHITIC ADDITION OF O
  185687. (PHENYLSULFANYL) PHENYLALKYNES
  185688. 1994 X    1907
  185689. 1911Z
  185690. 13298
  185691. GOODING, H.
  185692. J.C.S. Perkin Trans. 1C
  185693. GUANOSINE ANALOGS M
  185694. 14307N
  185695. 2/28/96
  185696. A^SYNTHESIS OF SOME CARBOCYCLIC NUCLEOSIDE ANALOGUES BASED ON A BICYCLO[3.1.0]HEXANE RING SYSTEM
  185697. 1994X    1891
  185698. 1892Z
  185699. 13299
  185700. MUKAIYAMA, T.
  185701. Chem. Lett.C
  185702. SILYL KETENE ACETALS ACID MEDIATED REACTIONS SIMPLE DIASTEREOSELECTION STEREOSELECTIVE SYNTHESIS ACYCLIC STEREOSELECTION CARBONYL
  185703. COMPOUNDS ENOL ETHERS ALDEHYDES CONDENSATION ESTERSM
  185704. 14308N
  185705. 2/28/96
  185706. COMBINED USE OF DIPHENYLTIN SULFIDE OR LAWESSON'S REAGENT AND SILVER PERCHLORATE AS EFFECTIVE CATALYST SYSTEMS IN ALDOL REACTION
  185707. 1994X
  185708. 13300
  185709. MAKIOKA, Y.
  185710. Chem. Lett.C
  185711. ALDOL COMPLEXES ALDEHYDES M
  185712. 14309N
  185713. 2/28/96
  185714. FACILE ISOMERIZATION OF TRIMETHYLSILYL KETENE ACETALS TO A
  185715. TRIMETHYLSILYL ESTERS CATALYZED BY LANTHANOID TRIFLUOROMETHANESULFONATES
  185716. 1994X
  185717. 13301
  185718. KOMATSU, K.
  185719. Chem. Lett.C
  185720. BUCKMINSTERFULLERENE C
  185721. 14310N
  185722. 2/28/96
  185723. ADENE REACTION AS A NEW METHOD FOR FUNCTIONALIZATION OF FULLERENE C
  185724. 1994 X
  185725. 13302
  185726. AKIYAMA, T.
  185727. Chem. Lett.C
  185728. CHIRAL (E)
  185729. CROTYLSILANES LEWIS ACID (TRIMETHYLSILYL)CYCLOPENTENE ANNULATION CYCLOPENTANE ANNULATION STEREOCHEMICAL COURSE CONJUGATE ADDITION M
  185730. 14311N
  185731. 2/28/96
  185732. STEREOSELECTIVE CONSTRUCTION OF TETRAHYDROFURAN BY TIN(IV) CHLORIDE PROMOTED [3+2] CYCLOADDITION OF ALLYLSILANE TO A
  185733. KETO ESTER
  185734. 1994X
  185735. 13303
  185736. A    NAGAO, Y.
  185737. Chem. Lett.M
  185738. 14312N
  185739. 2/28/96
  185740. NEW SIX
  185741.  TO EIGHT
  185742. MEMBERED
  185743. RING FORMATION BASED ON THE INTRAMOLECULAR ENDO
  185744.  MODE RING CLOSURE OF ALLENYL (SUBSTITUTED PHENYL)ALKYL KETONES
  185745. 1994 X
  185746. 13304
  185747. TSUNODA, T.
  185748. Chem. Lett.C
  185749. ISOIRIDOMYRMECIN M
  185750. 14313N
  185751. 2/28/96
  185752. AlA STEREOSELECTIVE SYNTHESIS OF (
  185753. ISOIRIDOMYRMECIN. APPLICATION OF THE ASYMMETRIC AZA
  185754. CLAISEN REARRANGEMENT
  185755. 1994 X
  185756. 13305
  185757. TSUNODA, T.
  185758. Chem. Lett.C
  185759. SULFONAMIDES ACIDS M
  185760. 14314N
  185761. 2/28/96
  185762. N,N,N',N'
  185763. TETRAMETHYLAZODICARBOXAMIDE (TMAD), A NEW VERSATILE REAGENT FOR MITSUNOBU REACTION. ITS APPLICATION TO SYNTHESIS OF SECONDARY AMINES
  185764. 1994X
  185765. 13306
  185766. A    OGAWA, S.
  185767. Chem. Lett.CUCYCLIC POLYSULFIDES BENZOPENTATHIEPIN VARACIN SULFUR 1,2,5
  185768. THIADISELENOLE LITHIATION M
  185769. 14315N
  185770. 2/28/96
  185771. AN EFFECTIVE AND SELECTIVE SYNTHESIS OF STERICALLY CROWDED BENZOTRITHIOLES FROM BENZODITHIASTANNOLES VIA BENZOTRITHIOLE 2
  185772. OXIDES
  185773. 1994 X
  185774. 13307
  185775. YASUDA, M.
  185776. Chem. Lett.C
  185777. COMPLEXES M
  185778. 14316N
  185779. 2/28/96
  185780. AOAMINATION OF O
  185781. ALKENYLPHENOLS WITH ALKYLAMINES VIA PHOTOINDUCED PROTON TRANSFER
  185782. 1994X
  185783. 13308
  185784. HOJO, M.
  185785. Chem. Lett.C1KETENE DITHIOACETALS ORGANIC
  185786. SYNTHESIS REDUCTION M
  185787. 14317N
  185788. 2/28/96
  185789. A NOVEL AND EFFICIENT GENERATION OF FUNCTIONALIZED VINYLCOPPER REAGENTS AND THEIR REACTIONS WITH ELECTROPHILES. SYNTHESIS OF b
  185790. METHYLTHIOBUTENOLIDES
  185791. 1994 X
  185792. 13309
  185793. WEINGES, K.
  185794. Chem. Ber.C
  185795. RADICALS CYCLOBUTANES M
  185796. 14318N
  185797. 2/28/96
  185798. RADICAL
  185799. TYPE CYCLIZATION OF DIENES .9. ON THE STEREOSELECTIVITY OF THE RADICAL 4
  185800. CYCLIZATION OF OPTICALLY ACTIVE ETHYL (2E)
  185801. OXOHEX
  185802. ENOATES WITH SAMARIUM(II) IODIDE
  185803. 1994 X    1305
  185804. 1309Y
  185805. 13310
  185806. SCHULTE, N.
  185807. Chem. Ber.
  185808. YNAMINES, N,N
  185809. BIS(TRIMETHYLSILYL)
  185810.  CYCLOADDITION REACTIONS CYCLOPROPENES FURANS KETENES CYCLOBUTENONES ALLENYLCARBOXAMIDES YNAMINES IDENTIFICATION MOLECULES M
  185811. 14319N
  185812. 2/28/96
  185813. AjN,N
  185814. BIS(TRIMETHYLSILYL)YNAMINES 
  185815.  CYCLOADDITION REACTIONS WITH DIMETHYL ACETYLENEDICARBOXYLANE AND KETENES
  185816. 1994 X    1287
  185817. 1293Y
  185818. 13311
  185819. WULFERDING, A.
  185820. Chem. Ber.C
  185821. KETENES (DIMERIC), REACTIONS WITH NUCLEOPHILES AND ELECTROPHILES TRISPIRO<2.1.2.1.2.1>DODECANE
  185822. 4,8,12
  185823. TRIONE CARBONYLCYCLOPROPANE SELENOXIDES KETENES M
  185824. 14320N
  185825. 2/28/96
  185826. ApSELECTED TRANSFORMATIONS OF 6
  185827. CYCLOPROPYLIDENE
  185828. OXASPIRO[2.3]HEXAN
  185829. ONE, A HIGHLY STRAINED TRICYCLIC b
  185830. LACTONE
  185831. 1994X    1275
  185832. 1281Y
  185833. 13312
  185834. VONSEGGERN, H.
  185835. KETENE CYCLOADDITIONS CYCLOHEPATIDENONES CARBOCATIONS REARRANGEMENTS TRANSFER CATALYZED
  185836. REACTIONS ELECTRON
  185837. TRANSFER CYCLOADDITION REACTION RADICAL CATIONS MECHANISM ETHYLENE M
  185838. 14321N
  185839. 2/28/96
  185840. A[ACID
  185841. INDUCED STEREOSELECTIVE FORMATION OF 3,5
  185842. CYCLOHEPTADIEN
  185843. ONES FROM KETENES AND DIENES
  185844. 13313
  185845. TOCHTERMANN, W.
  185846. Chem. Ber.C
  185847. PHOTOCHEMISTRY STEREOSELECTIVE BROMINATION DEOXYGENATION ALLYL
  185848. CYCLOPROPYL RING CLOSURE 2D
  185849. NMR 3,6
  185850. HEXANOOXEPIN
  185851. DICARBONIC ACID
  185852. ESTERS PHOTOCHEMICAL
  185853. REARRANGEMENT CHIRAL INDUCTION NMR
  185854. SPECTROSCOPY BENT BONDS M
  185855. 14322N
  185856. 2/28/96
  185857. AzSYNTHESIS OF MEDIUM AND LARGE RINGS .36. SYNTHESIS OF A BRIDGED BICYCLO[2.1.0]PENTANE DERIVATIVE WITH INSIDE CONFIGURATION
  185858. 1994 X    1263
  185859. 1267Y
  185860. 13314
  185861. MALISCH, W.
  185862. Chem. Ber.C
  185863. TAU 1
  185864. ALLYL IRON COMPLEXES 1,3
  185865. DIPOLAR CYCLOADDITION NITRILE OXIDES ISOXAZOLINES DIASTEREOSELECTIVE SYNTHESIS  1,3
  185866. DIPOLAR CYCLOADDITIONS CYCLOADDITIONS AMINO
  185867. SUGARS REACTIVITY DIPOLAROPHILESM
  185868. 14323N
  185869. 2/28/96
  185870. CYCLOADDITIONS OF ORGANOMETAL FRAGMENT
  185871. SUBSTITUTED ALKENES .1. [3+2] CYCLOADDITION OF h1
  185872. ALLYL IRON COMPLEXES WITH NITRILE OXIDES 
  185873.  FERRIOMETHYL
  185874. SUBSTITUTED ISOXAZOLINES
  185875. 1994 X    1243
  185876. 1246Y
  185877. 13315
  185878. POITRAS, J.
  185879. Can. J. Chem.CbMOLECULAR
  185880. STRUCTURES CRYSTAL
  185881. STRUCTURE COMPLEXES CHLORIDE LIGANDS METHYLMERCURY(II) ADDUCTS SALTS M
  185882. 14324N
  185883. 2/28/96
  185884. AsREACTIONS OF 7
  185885. AZAINDOLE WITH NIOBIUM AND TANTALUM PENTACHLORIDES AND COUPLING TO THE AZAINDOLYL
  185886. AZAINDOLIUM CATION
  185887. 1994X    1675
  185888. 1683Y
  185889. 13316
  185890. A    VOHRA, R.
  185891. Can. J. Chem.C+ORGANO
  185892. LITHIUM REAGENTS ALDEHYDES GRIGNARD M
  185893. 14325N
  185894. 2/28/96
  185895. ATENAMINES FROM FORMAMIDES. SYNTHESIS OF 1,2,3,4
  185896. TETRAHYDRO
  185897. SUBSTITUTED b
  185898. CARBOLINES
  185899. 1994 X    1660
  185900. 1667Y
  185901. 13317
  185902. GALATSIS, P.
  185903. Can. J. Chem.C    EPOXIDES M
  185904. 14326N
  185905. 2/28/96
  185906. AyINDENONE SYNTHESIS. IMPROVED SYNTHETIC PROTOCOL AND EFFECT OF SUBSTITUTION ON THE INTRAMOLECULAR FRIEDEL
  185907. CRAFTS ACYLATION
  185908. 1994X    1656
  185909. 1659Y
  185910. 13318
  185911. TIEN, H. J.
  185912. Can. J. Chem.C#SYDNONE COMPOUNDS SCHMIDT REACTION M
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  185914. 2/28/96
  185915. AvNITRATION OF 3
  185916. ACETYLSYDNONES: PREPARATION OF 3
  185917. NITROARYL)SYDNONES BY USING ACETYL GROUP AS A BLOCKING GROUP
  185918. 1994X    1610
  185919. 1613Y
  185920. 13319
  185921. BARLUENGA, J.
  185922. Angew. Chem. Int. Ed. Engl. M
  185923. 14328N
  185924. 2/28/96
  185925. AWASYMMETRIC MICHAEL ADDITIONS TO CHIRAL A,b
  185926. UNSATURATED ALKOXYCARBENE CHROMIUM COMPLEXES
  185927. 1994X    1392
  185928. 1394Y
  185929. 13320
  185930. MAZEAS, D.
  185931. Angew. Chem. Int. Ed. Engl. M
  185932. 14329N
  185933. 2/28/96
  185934. AwSAMARIUM IODIDE INDUCED INTRAMOLECULAR C
  185935. GLYCOSIDE FORMATION: EFFICIENT RADICAL FORMATION IN THE ABSENCE OF AN ADDITIVE
  185936. 1994X    1383
  185937. 1386Y
  185938. 13321
  185939. HERGES, R.
  185940. Angew. Chem. Int. Ed. Engl. M
  185941. 14330N
  185942. 2/28/96
  185943. ALMAGNETIC PROPERTIES OF AROMATIC TRANSITION STATES: THE DIELS
  185944. ALDER REACTIONS
  185945. 1994 X    1376
  185946. 1378Y
  185947. 13322
  185948. HOPF, H.
  185949. Angew. Chem. Int. Ed. Engl. M
  185950. 14331N
  185951. 2/28/96
  185952. A?1,1
  185953. , 1,2,3
  185954. , AND 1,1,4,4
  185955. TETRA
  185956. BUTYL
  185957. BUTADIENE
  185958. 1994X    1369
  185959. 1370Y
  185960. 13323
  185961. REDLICH, H.
  185962. Angew. Chem. Int. Ed. Engl. M
  185963. 14332N
  185964. 2/28/96
  185965. A"RING CONTRACTIONS IN CARBOHYDRATES
  185966. 1994 X    1345
  185967. 1347Y
  185968. 13324
  185969. BECKWITH, A. L. J.
  185970. J.C.S. Perkin Trans. 2C
  185971. ABSOLUTE RATE EXPRESSIONS HOMOLYTIC SUBSTITUTION RATE CONSTANTS RING
  185972. CLOSURE DECARBOXYLATIVE CHALCOGENATION DISPLACEMENT
  185973. REACTIONS THIOHYDROXAMIC ESTERS CARBOXYLIC
  185974. ACIDS CHAIN REACTIONS ATOM TRANSFER 
  185975. 14333N
  185976. 2/28/96
  185977. AVKINETICS OF INTRAMOLECULAR ALKYL RADICAL ATTACK ON SULFUR IN DISULFIDES AND THIOESTERS
  185978. 1994 X    1509
  185979. 1518Z
  185980. 13325
  185981. HARROWVEN, D. C.
  185982. Tet. Lett.C
  185983. KETENETHIOACETALS K
  185984. FURTHER STUDIES ON THE ADDITION OF CARBON CENTRED RADICALSTO KETENE DITHIOACETALS HAVE SHOWN THAT CYCLISATION MAYOCCUR TO EITHER THE SULFUR ATOM OR THE ALKENE MOIETY ANDTHAT THE OUTCOME IS GOVERNED BY THE AVAILABILITY OF A 5
  185985. EXO CYCLISATION PROCESS.M
  185986. 14334N
  185987. 2/28/96
  185988. AMDICHOTOMY IN THE ADDITION OF CARBON
  185989. CENTeRED RADICALS TO KETENE DITHIOACETALS
  185990. 1994 X    5301
  185991. 5302Y
  185992. 13326
  185993. A    ROSSI, L.
  185994. Tet. Lett.C
  185995. KETONES
  185996. aA GENERAL PROCEDURE FOR THE CONVERSION OF CYCLIC AND ACYCLIC ALPHA
  185997. ALKOXY
  185998.  CARBONYLAMINO)KETONES INTO THECORRESPONDING ''KINETIC'' SILYL ENOL ETHERS IN THE PRESENCE OF TRIMETHYLSILYLTRIFLATE AND A TERTIARY AMINE IS DESCRIBED. THE ADVANTAGE OF THE PRESENT METHOD CONSISTS OF AN ALMOST COMPLETE REGIOSELECTIVITY OBTAINED UNDER MILD REACTION CONDITIONS.
  185999. 14335N
  186000. 2/28/96
  186001. AfREGIOSPECIFIC PROCEDURE FOR THE PREPARATION OF SILYL ENOL ETHERS FROM A
  186002. ALKOXYCARBONYLAMINO)KETONES
  186003. 1994 X    5285
  186004. 5288Y
  186005. 13327
  186006. BRYCE, M. R.
  186007. Tet. Lett.CQTHIONITROSOARENES ARN=S DIELS
  186008. ALDER N
  186009. (ARYLAMINOTHIO) PHTHALIMIDES FRAGMENTATION K
  186010. A RANGE OF ALKYLTHIONITROSO AND ARYLTHIONITROSO COMPOUNDS HAVE BEEN GENERATED BY THERMAL FRAGMENTATION OF N
  186011. TRIMETHYLSILYL
  186012. CHLOROTHIOALKYL(ARYL) PRECURSORS, AND INTERCEPTED BY REACTION WITH DIMETHYLBUTADIENE TO AFFORD DIELS
  186013. ALDER AND ENE ADDUCTS.M
  186014. 14336N
  186015. 2/28/96
  186016. AqALKYLTHIONITROSO AND ARYLTHIONITROSO COMPOUNDS GENERATED FROM N
  186017. TRIMETHYLSILYL
  186018. CHLOROTHIO ALKYLAMINE PRECURSORS
  186019. 1994 X    5275
  186020. 5278Y
  186021. 13328
  186022. KOBAYASHI, M.
  186023. Tet. Lett.CILASER PHOTOCHEMISTRY HYPERVALENT IODINE MOLECULAR
  186024. OXYGEN 1,2,4
  186025. TRIOXANES 
  186026. ELECTROCHEMICALLY PREPARED N
  186027. CYCLOHEXADIENE
  186028. YLIDENE)
  186029. 2,2,2
  186030.  TRIFLUOROETHANIMIDAMIDES (P
  186031. BENZOQUINONE DERIVATIVES) (2) CYCLIZED ON HEATING IN DMSO AT 120 DEGREES C TO 2'
  186032. TRIFLUOROMETHYLSPIRO [2,5
  186033. CYCLOHEXADIENE
  186034. 1H(OR 3H)
  186035.  QUINAZOLIN] 4
  186036. ONES (SPIRODIENONE DERIVATIVES)(3) AND (4), WHICH WERE TRANSFORMED TO 1,5
  186037. DIAZEPINEDERIVATIVE (7) BY LEWIS ACID
  186038. CATALYZED DIENONE
  186039. PHENOL REARRANGEMENT.
  186040. 14337N
  186041. 2/28/96
  186042. THERMAL ELECTROCYCLIC SPIROCYCLIZATION OF P
  186043. BENZOQUINONEIMINES:  A NOVEL SYNTHETIC ROUTE TO TRIFLUOROMETHYLATED SPIRODIAZA CARBOCYCLES
  186044. 1994X    5235
  186045. 5238Y
  186046. 13329
  186047. DAVIES, H. M. L.
  186048. Tet. Lett.
  186049. C2CYCLOPROPANATION COPE REARRANGEMENT DECOMPOSITION K
  186050. INTRAMOLECULAR CAPTURE BY PYRROLES OF VINYL CARBENOIDS GENERATED BY RHODIUM(II) CARBOXYLATE CATALYZED DECOMPOSITION OF VINYL DIAZOMETHANES RESULTS IN THE FORMATION OF FUSED 7
  186051. AZABICYCLO[4.2.0]OCTADIENES OR FUSED TROPANES.M
  186052. 14338N
  186053. 2/28/96
  186054. RHODIUM(II) CATALYZED INTRAMOLECULAR REACTIONS BETWEEN VINYL DIAZOMETHANES AND PYRROLES. NOVEL SYNTHESIS OF FUSED 7
  186055. AZABICYCLO[4.2.0]OCTADIENES
  186056. 1994X    5209
  186057. 5212Y
  186058. 13330
  186059. NEWCOMB, M.
  186060. Tet. Lett.C
  186061. THIOHYDROXAMIC ESTERS HOMOALLYLIC ALCOHOLS CHAIN REACTIONS CARBONATES STEREOCHEMISTRY SELECTIVITY GENERATION INVENTION CHEMISTRY 
  186062. ALLYLIC AND HOMALLYLIC ALKOXYCARBONYLOXYL RADICALS, PRODUCED IN CHAIN REACTIONS OF 3
  186063. HYDROXY
  186064. METHYLTHIAZOLE
  186065. 2(3H)
  186066. THIONE CARBONATES, CYCLIZE TO GIVE, ULTIMATELY, 1,2
  186067. AND 1,3
  186068. DIOL CARBONATES IN FAIR TO GOOD YIELD AND, IN SOME CASES, HIGH DIASTEREOSELECTIVITY.
  186069. 14339N
  186070. 2/28/96
  186071. AWDIASTEREOSELECTIVE 1,2
  186072.  AND 1,3
  186073. DIOL FORMATION VIA OXYGEN
  186074. CENTERED RADICAL CYCLIZATIONS
  186075. 1994X    5193
  186076. 5196Y
  186077. 13331
  186078. ZHANG, W.
  186079. Tet. Lett.
  186080. STANNYL KETYLS RADICAL CYCLIZATION TRIMETHYLSILYL IODIDE HALOGENATED KETENES DICHLOROKETENE CYCLOADDITIONS EPOXY KETONES EXPANSION ADDITIONS ALDEHYDES 
  186081. CYCLOBUTANONE DICHLORO RADICAL CYCLIZATION NOVEL TRIMETHYLSILYL IODIDE CLEAVAGE INTRAMOLECULAR ANNULATION KETENE BICYCLIC
  186082. UFREE RADICAL ANNULATION FOLLOWED BY TRIMETHYLSILYL IODIDE
  186083. PROMOTED RING
  186084. OPENING OF (R)
  186085. CARVONE
  186086. DICHLOROKETENE ADDUCTS LEADS TO AN UNUSUAL CARBON SKELETON REARRANGEMENT.THE CARBONYL GROUP OF CARVONE ENHANCES THE REACTIVITY OFTHE RADICAL CYCLIZATION, CHANGES THE RING
  186087. OPENING PATHWAYAND LEADS TO THE FORMATION OF A NEW TRICYCLIC DIONE PRODUCT.
  186088. 14340N
  186089. 2/28/96
  186090. AkSTEREOSPECIFIC ANNULATION AND SEQUENTIAL RING
  186091. OPENING OF (R)
  186092. CARVONE:  FORMATION OF A NOVEL TRICYCLIC DIONE
  186093. 1994  X    5161
  186094. 5164Y
  186095. 13332
  186096. GRISSOM, J. W.
  186097. Tet. Lett.C
  186098. BIRADICAL FORMATION DNA CLEAVAGE 4
  186099. ALKYNYLCYCLOBUTENONES ALPHA,3
  186100. DEHYDROTOLUENE NEOCARZINOSTATIN TEMPERATURE GENERATION 
  186101. ENEYNE ALLENE 2,3 SIGMATROPIC SHIFT RADICAL BERGMAN CYCLIZATION ANTITUMOR ANTIBIOTICS SEQUENTIALKmENEYNE ALLENES GENERATED FROM [2,3] SIGMATROPIC SHIFTSWILL UNDERGO TANDEM ENEYNE ALLENE
  186102. RADICAL CYCLIZATIONS.M
  186103. 14341N
  186104. 2/28/96
  186105. AETANDEM ENEYNE ALLENE
  186106. RADICAL CYCLIZATION VIA [2,3] SIGMATROPIC SHIFTS
  186107. 1994 X    5137
  186108. 5140Y
  186109. 13333
  186110. LI, C.
  186111. Tet. Lett.
  186112. ERYTHRO
  186113. SPHINGANINE TRIACETATE CARBOHYDRATE REACTIONS MANNOSIDASE INHIBITOR SULFENYL HALIDES IODOCYCLOFUNCTIONALIZATION ACTIVATOR ANALOGS 
  186114.  THE STEREOSPECIFIC SYNTHESIS OF GLYCOPROTEIN PROCESSING ENZYME INHIBITOR (+) MANNOSTATIN A 1 WAS ACHIEVED IN TEN STEPS FROM D
  186115. RIBONOLACTONE 9 (SIMILAR TO 39% OVERALL YIELD). THE STRATEGY FEATURED METHANESULFENYL TRIFLATE MEDIATED INTRAMOLECULAR CYCLIZATION OF ALLYLIC N
  186116. SUFENYLIMIDATE 12.
  186117. 14342N
  186118. 2/28/96
  186119. METHANESULFENYL TRIFLATE PROMOTED IMINO SULFENYLATION OF AN ALLYLIC TRICHLOROACETIMIDATE. AN EFFICIENT AND STEREOSPECIFIC TOTAL SYNTHESIS OF (+) MANNOSTATIN A
  186120. 1994 X    5121
  186121. 5124Y
  186122. 13334
  186123. TSUNODA, T.
  186124. Tet. Lett.
  186125. CYANOMETHYLENETRIBUTYLPHOSPHORANE WAS SHOWN TO MEDIATE THE DIRECT CONDENSATION OF ALCOHOLS WITH O
  186126.  AND N
  186127. NUCLEOPHILES. A SECONDARY ALCOHOL, 2
  186128. OCTANOL, REACTED SATISFACTORILY WITH WALDEN INVERSION OF ITS CARBINYL CARBON.M
  186129. 14343N
  186130. 2/28/96
  186131. AUNOVEL REACTIVITY OF STABILIZED METHYLENETRIBUTYLPHOSPHORANE:  A NEW MITSUNOBU REAGENT
  186132. 1994X    5081
  186133. 5082Y
  186134. 13335
  186135. LYGO, B.
  186136. Tet. Lett.C<ACYL AZIRIDINE ACYLATING DIANION POLYDETIDES BETA KETO ESTER
  186137. A ONE
  186138. POT SYNTHESIS OF N
  186139. ACYLAZIRIDINES FROM CARBOXYLIC ACIDS HAS BEEN DEVELOPED, AND THEIR REACTION WITH DIANIONS DERIVED FROM BETA
  186140. KETOESTERS STUDIED. THE AZIRIDINES WERE FOUND TO BE EFFICIENT C
  186141. ACYLATING AGENTS, GIVING POLYKETIDE
  186142. LIKE PRODUCTS IN GOOD OVERALL YIELDS.
  186143. 14344N
  186144. 2/28/96
  186145. ACYL AZIRIDINES 
  186146. ACYLATING AGENTS FOR THE PREPARATION OF POLYKETIDES
  186147. 1994 X    5073
  186148. 5074Y
  186149. 13336
  186150. HUSSAIN, N.
  186151. Tet. Lett.CuEXPANSION
  186152. CYCLIZATION REACTIONS BOND FORMATION 
  186153. NITRATE ESTER FRAGMENTATION ALKOXY TIN RADICAL FRAGMENTATION SCISSIONK
  186154. THE FRAGMENTATION OF NITRATE ESTER (2) VIA AN ALKOXY RADICAL TO LACTONE (3) IS DESCRIBED. THIS LACTONE IS A KEY INTERMEDIATE IN THE SYNTHESIS OF SEMI SYNTHETIC MILBEMYCINS.M
  186155. 14345N
  186156. 2/28/96
  186157. AdALKOXY RADICALS IN ORGANIC SYNTHESIS. A NOVEL APPROACH TO A KEY INTERMEDIATE IN MILBEMYCIN CHEMISTRY
  186158. 1994 X    5069
  186159. 5072Y
  186160. 13337
  186161. COOPER, M. A.
  186162. Tet. Lett.CpN
  186163. PROTECTED 3
  186164. HYDROXY
  186165. PENTENYLAMINES NITROGEN
  186166. HETEROCYCLES 4
  186167. HYDROXY
  186168. HEXENYL AMINES HALOAMIDATION URETHANES 
  186169. xTHE SELENIUM INDUCED CYCLIZATION OF N
  186170. SUBSTITUTED 4
  186171. HYDROXY
  186172. HEXENYLAMINES OCCURS REGIO
  186173.  AND STEREOSELECTIVELY TO GIVE N
  186174. SUBSTITUTED TRANS
  186175. (PHENYLSELENOMETHYL)
  186176.  HYDROXYPIPERIDINES IN MODERATE YIELD. SYNTHESIS OF THE BIOLOGICALLY ACTIVE DIOL (8) WAS ACHIEVED VIA OXIDATION OF THE PHENYLSELENO MOIETY TO THE PHENYLSELENONE AND SUBSEQUENT DISPLACEMENT WITH SODIUM HYDROXIDE.
  186177. 14346N
  186178. 2/28/96
  186179. AWSELENIUM INDUCED STEREOSELECTIVE CYCLIZATION OF N
  186180. SUBSTITUTED
  186181. HYDROXY
  186182. HEXENYLAMINES
  186183. 1994X    5065
  186184. 5068Y
  186185. 13338
  186186. CARDILLO, G.
  186187. Tet. Lett.C.ASYMMETRIC
  186188. SYNTHESIS AMINO
  186189. ACIDS 1,4
  186190. ADDITION 
  186191. THE SYNTHESIS OF (R)
  186192. AMINOBUTANOIC ACID STARTING FROM CHIRAL ALPHA,BETA
  186193.  UNSATURATED IMIDE 1B IS DESCRIBED, BY MEANS OF THE NUCLEOPHILIC ATTACK OF SEVERAL PHTHALIMIDO DERIVATIVES IN THE PRESENCE OF A LEWIS ACID. THE REACTION WAS STUDIED IN SOME DETAILS AND CHLORO MAGNESIUM PHTHALIMIDE AFFORDED THE BETTER RESULTS WITH 95: 5DIASTEREOMERIC RATIO AND 90% YIELD. FURTHERMORE THERESULTING ENOLATE WAS TRAPPED PERFORMING THE REACTION IN THE PRESENCE OF BENZENESULFONYL BROMIDE AND THE 2
  186194. BROMO
  186195. PHTHALIMIDO DERIVATIVE 4 WAS OBTAINED IN GOOD YIELD AND
  186196. 14347N
  186197. 2/28/96
  186198. AKMICHAEL
  186199. TYPE ADDITION OF PHTHALIMIDE SALTS TO CHIRAL A,b
  186200. UNSATURATED IMIDES
  186201. 1994 X    5051
  186202. 5054Y
  186203. 13339
  186204. SATO, T.
  186205. Tet. Lett.C
  186206. KETONES K
  186207. ACID TREATMENT OF ALPHA
  186208. HYDROXY ACETALS INDUCED 1,2
  186209. ALKYL, ARYL, OR ALKENYL MIGRATION. AN ALKENYL MIGRATION PRODUCTWAS UTILIZED AS A STARTING MATERIAL OF METHYL L
  186210. MYCAROSIDE SYNTHESIS.M
  186211. 14348N
  186212. 2/28/96
  186213. A\ACYLOIN REARRANGEMENT OF A
  186214. HYDROXY ACETALS: APPLICATION TO THE METHYL L
  186215. MYCAROSIDE SYNTHESIS
  186216. 1994 X    5027
  186217. 5030Y
  186218. 13340
  186219. FUJIMOTO, K.
  186220. NAKAI B
  186221. Tet. Lett.
  186222. WITTIG RING CONTRACTION <2,3>
  186223. WITTIG SIGMATROPIC REARRANGEMENT ESTERS (+)
  186224. ARISTOLACTONE DERIVATIVES SYSTEM 
  186225. WITTIG SIGMATROPIC 2,3 REARRANGEMENT CHIRAL ENANTIOSELECTIVE ASYMMETRIC ESTER ENOLATE LIGAND
  186226. THE FIRST ENANTIOSELECTIVE VERSION OF THE ESTER ENOLATE [2,3] WITTIG REARRANGEMENT IS DESCRIBED WHICH INVOLVES A CHIRAL BORON ENOLATE WITH A CHIRAL BIS
  186227. SULFONAMIDE LIGAND TO PROVIDE A HIGH ENANTIOSELECTIVITY(>95%EE),  ALONG WITH A HIGH THREO DIASTEREOSELECTIVITY.
  186228. 14349N
  186229. 2/28/96
  186230. AUENANTIOSELECTIVE [2,3] WITTIG REARRANGEMENT INVOLVING A CHIRAL BORON ENOLATE TERMINUS
  186231. 1994 X    5019
  186232. 5022Y
  186233. 13341
  186234. A    Wu, M. J.B
  186235. Tet. Lett.
  186236. DTHE REACTION OF ALKYNYL BORANES, GENERATED IN SITU FROM LITHIUM ACETYLIDES AND BORON TRIFLUORIDE ETHERATE, WITH 3
  186237. BENZYL
  186238. TETRAHYDRO
  186239. OXAZINES AND 1,3
  186240. OXAZOLIDINES GAVE THE CORRESPONDING BETA
  186241. AMINOACETYLENES IN MODEST TO GOOD YIELD. BY THE EMPLOYMENT OF TITANIUM ACETYLIDES TO THESAME REACTION PROVIDED COMPARABLE RESULTS.
  186242. 14350N
  186243. 2/28/96
  186244. NUCLEOPHILIC RING OPENING OF TETRAHYDRO
  186245. OXAZINES AND 1,3
  186246. OXAZOLIDINES BY ALKYNYL ANIONS:  A NOVEL SYNTHESIS OF b
  186247. AMINOACETYLENES
  186248. 1994X    5003
  186249. 5004Y
  186250. 13342
  186251. HUISGEN, R.
  186252. Tet. Lett.C
  186253. KETENE IMINE THIOCARBONYL 
  186254. TOLYLOXYFURAN OR 2
  186255. METHOXYFURAN AND BTE, THE TITLECOMPOUND RAPIDLY ESTABLISH EQUILIBRIA WITH [2+2] AND/OR [4+2] CYCLOADDUCTS AS MONITORED BY F
  186256. 19 NMR ANALYSIS; FINALLY, THE IRREVERSIBLE OPENING OF THE FURAN RING AND CONCOMITANT CLOSURE OF A CYCLOPROPANE RING WINS. DISSOCIATION CONSTANTS OF FOUR TRANS
  186257. ADDUCTS AND ONE CIS
  186258. ADDUCT WERE MEASURED OVER A TEMPERATURE RANGE OF 90 DEGREES C;  THE REACTION ENTHALPIES AND ENTROPIES ART DISCUSSED.
  186259. 14351N
  186260. 2/28/96
  186261. AmDONOR
  186262. SUBSTITUTED FURANS AND 1,2
  186263. BIS(TRIFLUOROMETHYL) ETHYLENE
  186264. DICARBONITRILE:  THE HIDDEN CYCLOADDITIONS
  186265. 1994 X    4981
  186266. 4984Y
  186267. 13343
  186268. DESMAISON, G.
  186269. Tet. Lett.C
  186270. CYCLOADDITION URRUTIA
  186271. OPENING OF THE FURAN RING AND CONCOMITANT CLOSURE OF A CYCLOPROPANE RING WAS OBSERVED IN THE REACTION OF 2
  186272. METHOXY
  186273.  AND 2
  186274. TOLYLOXYFURAN WITH 2,3
  186275. BIS (TRIFLUORO METHYL) FUMARONITRILE (TRANS
  186276. BTE) .ELECTROPHILIC 5
  186277. ATTACK GIVES RISE TO A ZWITTERION WHICH CAN ROTATE ABOUT THE ACCEPTOR BOND, DISSOCIATE TO REACTANTS, OR FURNISH DIASTEREOISOMERIC CIS
  186278. CYCLOPROPYLACRYLATES. IN THE PRESENCE OF PYRIDINE, 1,3
  186279. PROTOTROPY CONVERTS THE ZWITTERION TO 5
  186280. SUBSTITUTED FURANS.
  186281. 14352N
  186282. 2/28/96
  186283. DONOR
  186284. SUBSTITUTED FURANS AND 1,2
  186285. BIS(TRIFLUOROMETHYL) ETHYLENE
  186286. DICARBONITRILE:  A NOVEL REARRANGEMENT AND ITS STERIC COURSE
  186287. 1994X    4977
  186288. 4980Y
  186289. 13344
  186290. BURK, M. J.
  186291. Tet. Lett.
  186292. C$HOMOGENEOUS HYDROGENATION COMPLEXES K
  186293. A CATIONIC RHODIUM(I) CATALYST BEARING THE AIR
  186294. STABLE AND CRYSTALLINE DIPHOSPHINE 1,1'
  186295. (DIISOPROPYLPHOSPHINO)FERROCENE (1, DIPFC) ALLOWS THE HYDROGENATION OF ALDEHYDES AND KETONES UNDER MILD CONDITIONS.M
  186296. 14353N
  186297. 2/28/96
  186298. ABEFFICIENT RHODIUM
  186299. CATALYZED HYDROGENATION OF ALDEHYDES AND KETONES
  186300. 1994X    4963
  186301. 4966Y
  186302. 13345
  186303. A    Su, W. G.B
  186304. Tet. Lett.CISULFIDE SULFONE EXPERIMENTAL REAGENT OXIDATION RUTHENIUM SODIUM PERIODATEK
  186305. RUTHENIUM TRICHLORIDE 
  186306.  SODIUM PERIODATE IS A HIGHLY EFFICIENT AND POWERFUL SYSTEM FOR THE OXIDATION OF UNREACTIVE SULFIDES TO SULFONES.M
  186307. 14354N
  186308. 2/28/96
  186309. A=AN EFFICIENT METHOD FOR THE OXIDATION OF SULFIDES TO SULFONES
  186310. 1994X    4955
  186311. 4958Y
  186312. 13346
  186313. ELWORTHY, T. R.
  186314. Tet. Lett.C*ALLYL ESTERS ALCOHOLS ANALOGS BONDS ACIDS 
  186315. %ALPHA
  186316. HETEROATOM SUBSTITUTED ORTHOESTERS WERE PREPARED ANDFOUND TO UNDERGO THE JOHNSON CLAISEN REARRANGEMENT WITH A VARIETY OF ALLYLIC ALCOHOLS GIVING GAMMA,DELTA
  186317.  UNSATURATED ALPHA
  186318. HETEROATOM SUBSTITUTED ESTERS IN FAIR TO EXCELLENT YIELDS. THE DIASTEREOSELECTIVITY OF THE PROCESS WASEXAMINED.
  186319. 14355N
  186320. 2/28/96
  186321. A\ON THE UTILITY OF A
  186322. HETEROATOM SUBSTITUTED ORTHO ESTERS IN THE JOHNSON CLAISEN REARRANGEMENT
  186323. 1994X    4951
  186324. 4954Y
  186325. 13347
  186326. RAWAL, V. H.
  186327. Tet. Lett.CpSYNTHETIC METHODS 
  186328. AZIDE ACYL ESTER CONVERSION DIETHYLALUMINUM ALUMINUM CURTIUS PREPARATION REARRANGEMENT REVIEWK
  186329. DIETHYLALUMINUM AZIDE, PREPARED FROM EITHER SODIUM AZIDE AND DIETHYLALUMINUM CHLORIDE OR HYDRAZOIC ACID AND TRIETHYLALUMINUM, REACTS WITH ESTERS TO YIELD ACYL AZIDES IN ONE STEP.M
  186330. 14356N
  186331. 2/28/96
  186332. AHONE
  186333. STEP CONVERSION OF ESTERS TO ACYL AZIDES USING DIETHYLALUMINUM AZIDE
  186334. 1994X    4947
  186335. 4950Y
  186336. 13348
  186337. ROMEO, S.
  186338. RICHB
  186339. Tet. Lett.C
  186340. STEREOCONTROLLED SYNTHESIS DIPEPTIDE ISOSTERES PROTEASE INHIBITORS HIV
  186341. 1 PROTEASE EPOXIDATION CONFIGURATION ROUTES AMIDES ACIDS RENIN 
  186342. EPOXIDE EPOXIDATION ALLYL AMINE DIASTEREOSELECTIVE RING OPENING MCPBA PERACID
  186343. THE MECHANISM OF EPOXIDATION OF CHIRAL ALLYL AMINES HAS BEEN INVESTIGATED. THE INTRINSIC STEREOSELECTIVITY FOR EPOXIDATION IS SHOWN TO BE APPROXIMATELY 5: 1 AND IS INDEPENDENT OF THE NITROGEN SUBSTITUENT. HOWEVER, THE NATURE OF THE N
  186344. PROTECTING GROUP INFLUENCES THE STABILITYOF THE UNDESIRED EPOXIDE TO THE ACIDIC MEDIA, WITH THE MINOR DIASTEREOMER UNDERGOING PREFERENTIAL DECOMPOSITION.CONDITIONS ARE REPORTED FOR THE HIGHLY STEREOSELECTIVE SYNTHESIS OF EPOXIDE 9R, AN IMPORTANT BUILDING BLOCKB. INTHE SYNTHESIS OF SEVERAL ENZYME INHIBITORS.
  186345. 14357N
  186346. 2/28/96
  186347. A;STEREOSELECTIVE SYNTHESIS OF PROTECTED AMINO ALKYL EPOXIDES
  186348. 1994 X    4939
  186349. 4942Y
  186350. 13349
  186351. ZHANG, H. C.
  186352. Tet. Lett.
  186353. ALPHA
  186354. SUBSTITUTED ALKANONES ACID
  186355. PROMOTED REACTIONS MEDIUM
  186356. SIZED RING STEREOSELECTIVE SYNTHESIS DIASTEREOSELECTIVE REDUCTION DIRECTED REDUCTION ALDEHYDES ESTERS STEREOCHEMISTRY HYDROSILANES 
  186357. A VARIETY OF REDUCING AGENTS WAS EXPLORED TO EFFECT STEREOSELECTIVE REDUCTION OF ACYCLIC DELTA
  186358. HYDROXY KETONE 3A;  R
  186359. ALPINE
  186360. HYDRIDE PROVIDED HIGH ANTI STEREOSELECTIVITY(ANTI: SYN = 7: 1). REDUCTION OF 3B IN CH2CL2 WITH R
  186361. ALPINE
  186362. HYDRIDE OR ZN(BH4)(2) AFFORDED IMPRESSIVE ANTISTEREOSELECTIVITY:  10: 1 AND 13: 1, RESPECTIVELY. THESTEREOCHEMICAL OUTCOME IS ATTRIBUTED TO A BICYCLIC METAL
  186363. CHELATE SPECIES (VIZ. 10).
  186364. 14358N
  186365. 2/28/96
  186366. REMOTE ACYCLIC DIASTEREOCONTROL INVOLVING A BICYCLIC METAL CHELATE. HIGH 1,5 ASYMMETRIC INDUCTION IN THE HYDRIDE REDUCTION OF d
  186367. HYDROXY KETONES
  186368. 1994X    4891
  186369. 4894Y
  186370. 13350
  186371. MAJETICH, G.
  186372. Tet. Lett.CwANNULATIONS 
  186373. FURAN CYCLIZATION ENONE LEWIS ACID CYCLOPENTENONE INTRAMOLECULAR CYCLIALKYLATION VINYL CONJUGATED DIENONESK
  186374. FUSED TRICYCLIC COMPOUNDS WITH THE SALIENT FEATURES OF THE GUAIANOLIDES AND THE PSEUDOGUAIANOLIDES WERE PREPARED USING A FURAN
  186375. BASED CYCLIALKYLATION STRATEGY.M
  186376. 14359N
  186377. 2/28/96
  186378. A3CYCLIALKYLATIONS OF CONJUGATED DIENONES WITH FURANS
  186379. 1994 X    4887
  186380. 4890Y
  186381. 13351
  186382. NEBOIS, P.
  186383. TetrahedronCi1
  186384. AZADIENE O
  186385. QUINONE DIELS
  186386. ALDER OXIDATION FUROQUINOLINEDIONE DIELS
  186387. ALDER REACTIONS QUINONES TANSHINONES 
  186388. THE REACTIONS OF 2
  186389. ETHOXYBUT
  186390. ENAL N,N
  186391. DIMETHYLHYDRAZONE WITH QUINOLINE
  186392. DIONES OR BENZO[1,2
  186393. B]FURAN
  186394. DIONES THROUGH A [3+2] PROCESS OR A [4+2] CYCLOADDITION OFFER TWO EFFICIENT AND REGIOSPECIFIC ROUTES TO SUBSTITUTED FURO[2,3
  186395. F]QUINOLINE
  186396. DIONES. ASSIGNEMENT OF THE STRUCTURE AND THE REGIOCHEMISTRY OF THE DIELS
  186397. ALDER PRODUCTS IS MADE BY 1D H
  186398. 1 NOE DIFF AND 2D H
  186399. 13 HMBC NMR EXPERIMENTS.
  186400. 14360N
  186401. 2/28/96
  186402. ETHOXYBUT
  186403. ENAL N,N
  186404. DIMETHYLHYDRAZONE:  A USEFUL REAGENT FOR THE SYNTHESIS OF FURO[2,3
  186405. F]QUINOLINE
  186406. DIONES
  186407. 1994 X    8457
  186408. 8464Y
  186409. 13352
  186410. ROUX, M. C.
  186411. TetrahedronC"CATALYZED ENE REACTIONS ALDEHYDES 
  186412. LEWIS ACID CATALYZED CYCLIZATION OF LACTONES 1 
  186413.  4 ORCYCLOHEXANONE 5 BEARING TRANS VICINAL AROYL AND ALLYLIC MOIETIES PROVIDED STEREOSELECTIVELY FUNCTIONALIZED TRANSFUSED RING LACTONES AND CYCLOHEXANONES AS WELL AS AROMATIC ANALOGUES IN HIGH YIELDS. CYCLIZATION OF 1 LEADS TO ASINGLE STEREOMER OF 7
  186414. CHLORO
  186415. HYDROXYOCTAHYDROISOCOUMARIN 6 EXCLUSIVELY OR 5
  186416. HYDROXYISOCOUMARIN 9 PREDOMINANTLY DEPENDING ON THE LEWIS ACIDNATURE WHILE 4 GIVES EXCLUSIVELY METHYLENE OCTAHYDROISOCOUMARIN 10 OR DIHYDROB
  186417. ISOCOUMARIN 11 ACCORDING
  186418. 14361N
  186419. 2/28/96
  186420. ABEASY ACCESS TO HIGHLY FUNCTIONALIZED BICYCLIC LACTONES AND KETONES
  186421. 1994X    8445
  186422. 8456Y
  186423. 13353
  186424. HASHIMOTO, Y.
  186425. Tetrahedron
  186426. CrSILYLATED CARBON NUCLEOPHILES ALDOL
  186427. TYPE REACTION ACETALS SELECTIVITY LIMITATION CHEMISTRY ADDITIONS ETHERS SCOPE 
  186428. (MESITYLTHIO)ALKYL] BENZALDEHYDES AND THEIR DIMETHYLACETALS REACT WITH SILYLATED CARBON NUCLEOPHILES UNDER LEWIS ACIDIC CONDITIONS TO GIVE THE CORRESPONDING ALDOLADDUCTS WITH HIGH DIASTEREOSELECTIVITY, AND IN SOME CASES,THE PRODUCTS WERE OBTAINED AS ALMOST A SINGLE DIASTEREOMER. SUCH A HIGH DIASTEREOSELECTIVITY IS INTERPRETED AS THE RESULT OF THE 1,4
  186429. REMOTE ASYMMETRICINDUCTION THROUGH THE BENZENE RING FROM THE CHIRAL ORTHOSUBSTITUENTS OF THE SUBSTRATES TO THE REACTION CENTERS. INTHE SB-AME MANNER, GAMMA
  186430. MESITYL THIOLATED ALIPHATIC
  186431. 14362N
  186432. 2/28/96
  186433. AUREMOTE ASYMMETRIC INDUCTION USING NEIGHBORING GROUP PARTICIPATION OF A SULFENYL GROUP
  186434. 1994X    8317
  186435. 8336Y
  186436. 13354
  186437. HATANAKA, Y.
  186438. TetrahedronCpPALLADIUM
  186439. CATALYZED REACTION BOND FORMATION ARYLBORONIC ACIDS HINDERED BIARYLS FLUORIDE
  186440. ION STRATEGIES TRIFLATE 
  186441. THE PALLADIUM CATALYZED CROSS
  186442. COUPLING REACTION OF ARYLHALIDES WITH ARYL(HALO)SILANES (HALOGEN= F, CL) GIVES GOOD YIELDS OF UNSYMMETRICAL BIARYLS AND P
  186443. TERPHENYLS. THE REACTION TAKES PLACE SMOOTHLY IN N,N
  186444. DIMETHYLFORMAMIDE INTHE PRESENCE OF AN APPROPRIATE PALLADIUM CATALYST ANDPOTASSIUM FLUORIDE. SINCE THIS REACTION IS TOLERANT OF A VARIETY OF REACTIVE FUNCTIONAL GROUPS, HIGHLY FUNCTIONALIZED 4,4'
  186445. , 3,4'
  186446. , 2,4'
  186447.  AND EVEN STERICALLYCROWDED 2,2'
  186448. DISUBSTITUTED BIARYLS CAN BE OBTAINED INMODERAB/TE TO HIGH YIELDS. THE SYNTHETIC UTILITY OF THE
  186449. 14363N
  186450. 2/28/96
  186451. HIGHLY SELECTIVE CROSS
  186452. COUPLING REACTIONS OF ARYL(HALO)SILANES WITH ARYL HALIDES:  A GENERAL AND PRACTICAL ROUTE TO FUNCTIONALIZED BIARYLS
  186453. 1994X    8301
  186454. 8316Y
  186455. 13355
  186456. GUZZO, P. R.
  186457. TetrahedronC
  186458. SULFONYLATED HYDROXAMIC ACIDS ENANTIOSELECTIVE SYNTHESIS MITSUNOBU REACTIONS PRIMARY AMINES ALPHA LORACARBEF AMIDES EPIMERIZATION INTERMEDIATE ANTIBIOTICS 
  186459. INTRAMOLECULAR NUCLEOPHILE TRANSFER REACTION OF SEVERAL N
  186460. TOSYLOXY BETA
  186461. LACTAMS WAS APPLIED TO CONSTRUCT A NEW SIX
  186462. MEMBERED RING IN THE PRODUCT BICYCLIC BETA
  186463. LACTAMS. THEBICYCLIC PRODUCTS GENERALLY POSSESSED CIS STEREOCHEMISTRY ON THE BETA LACTAM RING. THE MAJOR COMPETING PROCESS APPEARED TO BE AN INTRAMOLECULAR S
  186464. N REACTION OF THENUCLEOPHILE AT THE C4 CARBON OF THE N
  186465. TOSYLOXY BETA
  186466. LACTAM AND ACCOUNTED FOR THE LOW YIELD OF THE DESIRED BICYCLIC PRODUCTS. VARIOUS BY
  186467. PRODUCTS FROM THE REACTIOB>N WEREISOLATED AND CHARACTERIZED WHICH SUPPORTED THE MECHANISM
  186468. 14364N
  186469. 2/28/96
  186470. AnSYNTHESES OF NOVEL BICYCLIC b
  186471. LACTAMS BY INTRAMOLECULAR NUCLEOPHILE TRANSFER REACTIONS OF N
  186472. TOSYLOXY b
  186473. LACTAMS
  186474. 1994X    8275
  186475. 8292Y
  186476. 13356
  186477. UDDING, J. H.
  186478. TetrahedronC/DERIVATIVES FRAGMENTATION CYCLIZATION NITROGEN 
  186479. AN EFFICIENT CU(BPY)CL
  186480. CATALYSED N
  186481. ACYLIMINIUM ION CYCLISATION TO N
  186482. PROTECTED 3
  186483. AZABICYCLO [3.3.1]NON
  186484. ENE IS REPORTED. THIS COMPOUND HAS BEEN DEMONSTRATED TO BE AVALUABLE INTERMEDIATE IN THE SYNTHESIS OF 2,4
  186485. DISUBSTITUTED 1
  186486. ADAMANTANES, AND LED TO A STEREOSELECTIVE SYNTHESIS OF 1
  186487. ADAMANTAN
  186488. OL. THISSELECTIVITY WAS ALSO OBSERVED IN THE SYNTHESIS OF TWO A
  186489. AMINO ACID DERIVATIVES WITH THE ADAMANTANE SKELETON. AN X
  186490. RAY CRYSTAL STRUCTURE OF ONE OF THE CYCLISATION PRODUCTSIS PRESENTED.
  186491. 14365N
  186492. 2/28/96
  186493. COPPER
  186494. CATALYSED N
  186495. ACYLIMINIUM ION CYCLISATION TO 3
  186496. AZABICYCLO[3.3.1]NONANES;  SYNTHESIS OF 2,4
  186497. DISUBSTITUTED 1
  186498. ADAMANTANES
  186499. 1994 
  186500. X    8853
  186501. 8862Y
  186502. 13357
  186503. GENNARI, C.
  186504. TetrahedronC
  186505. QUATERNARY STEREOGENIC CENTERS CHIRAL ALDEHYDES DIASTEREOSELECTIVE ADDITION DIASTEREOFACIAL SELECTIVITY ALLYLBORATION REACTION ASYMMETRIC INDUCTION CONFORMATIONAL SPACE MOLECULAR MECHANICS ALDOL REACTION ALCOHOLS 
  186506. A MOLECULAR MECHANICS MODEL OF THE TRANSITION STATE FOR THE ADDITION OF ALLYL AND CROTYL BORONATES TO ALDEHYDES WAS DEVELOPED, BASED ON AB INITIO CALCULATIONS AND ON APROCESS OF VIAL AND ERROR OPTIMIZATION. THE OPTIMIZED FORCE FIELD REPRODUCES THE EXPERIMENTAL SYN
  186507. ANTI STEREOSELECTIVITY FOR THE INTERMOLECULAR ADDITION OF E ANDZ CROTYL BORONATES TO ALDEHYDES. THE FORCE FIELD IS USED TO ANALYSE THE STEREOSELECTIVITY OF VARIOUS SYNTHETICALLY INTERESTING REACTIONS. IN PARTICULAR, THE FORCE FIEB<LD ISABLE TO REPRODUCE WITH EXCELLENT QUANTITATIVE AGREEMENT
  186508. 14366N
  186509. 2/28/96
  186510. ORIGINS OF STEREOSELECTIVITY IN THE ADDITION OF ALLYL AND CROTYLBORONATES TO ALDEHYDES:  THE DEVELOPMENT AND APPLICATION OF A FORCE FIELD MODEL OF THE TRANSITION STATE
  186511. 1994 X    8815
  186512. 8826Y
  186513. 13358
  186514. BURY, P.
  186515. TetrahedronM
  186516. 14367N
  186517. 2/28/96
  186518. AJTWO SYNTHESES OF MANOALIDE VIA HETEROATOM
  186519. ASSISTED ALKYNE CARBOMETALLATION
  186520. 1994 X    8793
  186521. 8808Y
  186522. 13359
  186523. CHEN, S. H.
  186524. TetrahedronC3NUDE
  186525. MICE CHEMISTRY DERIVATIVES AGENT ANALOGS BETA 
  186526. IRRADIATION OF TAXOL AT 280 NM IN A RAYONET REACTOR YIELDED A NOVEL PENTACYCLIC DERIVATIVE CONTAINING A NEWBOND BETWEEN C
  186527. 3 AND C
  186528. II. THE PROPOSED MECHANISM INVOLVESA TRIPLET INTERMEDIATE AND THE FIRST EVENT OF THE OXA
  186529. MERHANE REARRANGEMENT. TAXANE DERIVATIVES THAT LACK BOTH THE BENZOATE AT C
  186530. 2 AND THE BENZAMIDE FUNCTION AT C
  186531. 3' DO NOT UNDERGO THE REARRANGEMENT, SUGGESTING THE INTERVENTION OF AN INTRAMOLECULAR ENERGY TRANSFER.IRRADIATION AT 300 NM ALSO EFFECTS EXTRUSION OF THE C
  186532. 9CARB*BONYL, YIELDING A RING
  186533. CONTRACTED PRODUCT.
  186534. 14368N
  186535. 2/28/96
  186536. A)STUDIES ON THE PHOTOCHEMISTRY OF TAXOL(R)
  186537. 1994 X    8633
  186538. 8650Y
  186539. 13360
  186540. Kim, T. H.B
  186541. Syn. Commun.C
  186542. CARBANIONS M
  186543. 14369N
  186544. 2/28/96
  186545. AzREACTION OF PUMMERER REARRANGEMENT INTERMEDIATE WITH THIOLS 
  186546.  NEW SYNTHETIC METHOD OF S,S
  186547. THIOACETALS OF FORMYLPHOSPHONATE
  186548. 1994X    2313
  186549. 2318Y
  186550. 13361
  186551. CHOI, H. C.
  186552. Syn. Commun.M
  186553. 14370N
  186554. 2/28/96
  186555. A]FACILE CLEAVAGE OF N,N
  186556. DIMETHYLHYDRAZONES TO KETONES USING TETRABUTYLAMMONIUM PEROXYDISULFATE
  186557. 1994X    2307
  186558. 2311Y
  186559. 13362
  186560. BEDEKAR, A. V.
  186561. Syn. Commun.C
  186562. ACETATE M
  186563. 14371N
  186564. 2/28/96
  186565. A,NEW, SIMPLE 1,2
  186566. IODOACETOXYLATION OF ALKENES
  186567. 1994X    2299
  186568. 2305Y
  186569. 13363
  186570. GUNGOR, T.
  186571. Syn. Commun.M
  186572. 14372N
  186573. 2/28/96
  186574. A7NEW SYNTHESIS OF 1
  186575. SUBSTITUTED 3
  186576. AMINOETHYL) INDOLES
  186577. 1994X    2247
  186578. 2256Y
  186579. 13364
  186580. CAVICCHIONI, G.
  186581. Syn. Commun.M
  186582. 14373N
  186583. 2/28/96
  186584. AdBROMOAMIDES AS STARTING MATERIALS IN THE SYNTHESIS OF A
  186585. HYDROXY DERIVATIVES AND A
  186586. ALKOXY DERIVATIVES
  186587. 1994X    2223
  186588. 2227Y
  186589. 13365
  186590. TENHOEVE, W.
  186591. Syn. Commun.M
  186592. 14374N
  186593. 2/28/96V
  186594. CHIRAL CYCLIC AMIDINESW
  186595. 1994X    2215
  186596. 2221Y
  186597. 13366
  186598. A    Wu, S. H.B
  186599. Syn. Commun.C&SAMARIUM TRICHLORIDE REAGENT CLEAVAGE M
  186600. 14375N
  186601. 2/28/96
  186602. AUA FACILE METHOD FOR THE TRANSFORMATION OF ACETALS AND KETALS TO ALDEHYDES AND KETONES
  186603. 1994X    2173
  186604. 2177Y
  186605. 13367
  186606. PARSONS, P. J.
  186607. Syn. Commun.M
  186608. 14376N
  186609. 2/28/96
  186610. AzTHE GENERATION OF DOUBLE BONDS OF SPECIFIC GEOMETRY BY REGIOSELECTIVE ADDITION OF ORGANOTIN CUPRATES TO PROPARGYLIC ETHERS
  186611. 1994X    2159
  186612. 2165Y
  186613. 13368
  186614. GEORG, G. I.
  186615. 14377N
  186616. 2/28/96
  186617. A]SAMARIUM DIIODIDe MEDIATED DEOXYGENATION OF TAXOL:  A ONE
  186618. STEP SYNTHESIS OF 10
  186619. DEACETOXYTAXOL
  186620. 1994 X    4015
  186621. 4018Y
  186622. 13369
  186623. KATSUHIRA, T.
  186624. 14378N
  186625. 2/28/96
  186626. NEW METHOD FOR GENERATION OF ALKENYLIDENE CARBENES FROM PROPARGYLIC METHANESULFONATES AND ITS USE IN REGIOSELECTIVE C
  186627. H INSERTION REACTIONS
  186628. 1994X    4010
  186629. 4014Y
  186630. 13370
  186631. HUTCHINS, R. O.
  186632. 14379N
  186633. 2/28/96
  186634. AYPREPARATION OF N
  186635. DIPROTECTED ALLYLIC AMINES VIA PALLADIUM(0)
  186636. CATALYZED COUPLING REACTIONS
  186637. 1994 X    4007
  186638. 4009Y
  186639. 13371
  186640. GRACIA, J.
  186641. STRYCHNOS INDOLE ALKALOIDS MODIFIED POLONOVSKI REACTION FUNCTIONALIZED 2
  186642. AZABICYCLO<3.3.1>NONANES RING
  186643. SYSTEM DIMETHYL(METHYLTHIO)SULFONIUM FLUOROBORATE STEREOSELECTIVE SYNTHESIS HETEROCYCLIC COMPOUNDS FISCHER INDOLIZATION ROUTE TUBOTAIWINE M
  186644. 14380N
  186645. 2/28/96
  186646. ATTOTAL SYNTHESIS OF ULEINE
  186647. TYPE AND STRYCKNOS ALKALOIDS THROUGH A COMMON INTERMEDIATE
  186648. 1994 X    3939
  186649. 3951Y
  186650. 13372
  186651. PARKER, K. A.
  186652. REARRANGEMENT M
  186653. 14381N
  186654. 2/28/96
  186655. A\THE RADICAL CYCLIZATION APPROACH TO MORPHINE. MODELS FOR HIGHLY OXYGENATED RING
  186656. III SYNTHONS
  186657. 1994 X    3933
  186658. 3938Y
  186659. 13373
  186660. PARKER, K. A.
  186661. MODIFIED CURTIUS REACTION CONVENIENT REAGENT ORGANIC
  186662. SYNTHESIS REDUCING AGENT TRIS(TRIMETHYLSILYL)SILANE (
  186663. MORPHINE REDUCTION ALKENES KETONES ESTERS M
  186664. 14382N
  186665. 2/28/96
  186666. AzSTEREOCHEMISTRY OF RADICAL CYCLIZATIONS TO SIDE
  186667. CHAIN OLEFINIC BONDS. AN APPROACH TO CONTROL OF THE C
  186668. 9 CENTER OF MORPHINE
  186669. 1994 X    3927
  186670. 3932Y
  186671. 13374
  186672. SONG, Z. Z.
  186673. CROSS
  186674. COUPLING REACTION AUSTRALIAN MARINE SPONGE ORGANO
  186675. SILICON COMPOUNDS ARYL BORONIC ACIDS ORGANOSILICON COMPOUNDS EFFICIENT SYNTHESIS PALLADIUM CATALYST CRYSTAL
  186676. STRUCTURE FLUORIDE
  186677. ION CHEMISTRY M
  186678. 14383N
  186679. 2/28/96
  186680. SYNTHESIS AND REACTIONS OF 3,4
  186681. BIS(TRIMETHYLSILYL)FURAN: DIELS
  186682. ALDER CYCLOADDITION, FRIEDEL
  186683. CRAFTS ACYLATION, AND REGIOSPECIFIC CONVERSION TO 3,4
  186684. DISUBSTITUTED FURANS
  186685. 1994X    3917
  186686. 3926Y
  186687. 13375
  186688. ARJONA, O.
  186689. `DIELS
  186690. ALDER REACTION PLATELET
  186691. ACTIVATING
  186692. FACTOR DERIVATIVES NAKED SUGARS RING
  186693. OPENING REACTIONS ASYMMETRIC
  186694. SYNTHESIS STEREOCONTROLLED SYNTHESIS STEREOSELECTIVE SYNTHESIS ORGANOMETALLIC REAGENTS SUBSTITUTED CYCLOHEXENEDIOLS STEREOSPECIFIC SYNTHESIS 
  186695. OXABICYCLIC RING OPENING WRITING INTRODUCTION VINYL SULFONE ADDITION ELIMINATION ALKYLLITHIUM CONJUGATE
  186696. 14384N
  186697. 2/28/96
  186698. AeSULFONE DIRECTED ALKYLATIVE BRIDGE CLEAVAGE OF OXABICYCLIC VINYL SULFONES WITH ORGANOLITHIUM REAGENTS
  186699. 1994X    3906
  186700. 3916Y
  186701. 13376
  186702. ZIEGER, H. E.
  186703. TERTIARY ALKYL CHLORIDES ACID M
  186704. 14385N
  186705. 2/28/96
  186706. AYTITANIUM(IV) CHLORIDE CATALYZED CYANATION OF BENZYLIC HALIDES WITH TRIMETHYLSILYL CYANIDE
  186707. 1994X    3838
  186708. 3840Y
  186709. 13377
  186710. KIRMSE, W.
  186711. FUNCTIONALIZED ARYLCARBENES PHENYLCARBENE REARRANGEMENT ADDITION
  186712. REACTIONS SOLVENT POLARITY CARBON GENERATION INSERTION CARBENES BENZOCYCLOBUTENES PHOTOLYSIS M
  186713. 14386N
  186714. 2/28/96
  186715. AIINTRAMOLECULAR REACTIVITY OF ARYLCARBENES:  DERIVATIVES OF O
  186716. TOLYLCARBENE
  186717. 1994X    3821
  186718. 3829Y
  186719. 13378
  186720. ADAM, W.
  186721. RESOLVED PHOTOACOUSTIC CALORIMETRY UV
  186722. LASER PHOTOCHEMISTRY AZO BRIDGES TRIPLET DIRADICALS ORGANIC
  186723. MOLECULES DEFICIENT DIENES SPIN RESONANCE NITROGEN LOSS LIFETIMES 1,3
  186724. CYCLOPENTANEDIYL M
  186725. 14387N
  186726. 2/28/96
  186727. ELECTRONIC SUBSTITUENT EFFECTS ON THE ACID
  186728. CATALYZED [4(+)+2] CYCLOADDITION OF ISOPYRAZOLES WITH CYCLOPENTADIENE AND THE PHOTOCHEMICAL AND THERMAL DENITROGENATION OF THE RESULTING 1,4
  186729. DIARYL
  186730. DIMETHYL
  186731. DIAZABICYCLO[2.2.1]HEPT
  186732. ENE AZOALKANES TO
  186733. 1994 X    3786
  186734. 3797Y
  186735. 13379
  186736. DUFFY, J. L.
  186737. KURTH 
  186738. ORGANIC
  186739. SYNTHESIS CYCLOADDITIONS NITRILE OXIDES TETRAHYDROFURANS LITHIUM 
  186740. NITRILE OXIDE NITRONATE SILYL DIPOLAR CYCLOADDITION INTRODUCTION NITRO ISOXAZOLEM
  186741. 14388N
  186742. 2/28/96
  186743. AkA NOVEL INTRAMOLECULAR SILYL NITRONATE CYCLOADDITION ROUTE TO DIHYDROFURALDEHYDES AND DIHYDROPYRANALDEHYDES
  186744. 1994 X    3783
  186745. 3785Y
  186746. 13380
  186747. KOBAYASHI, S.
  186748. JOCCMTRIFLUOROMETHANESULFONATE SC(OTF)3 LEWIS
  186749. ACID REAGENT COMPLEXES SYSTEM ALDOL M
  186750. 14389N
  186751. 2/28/96
  186752. AEA CHIRAL SCANDIUM CATALYST FOR ENANTIOSELECTIVE DIELS
  186753. ALDER REACTIONS
  186754. 1994 X    3758
  186755. 3759Y
  186756. 13381
  186757. JONES, D. K.
  186758. CFSTEREOCONTROLLED SYNTHESIS CARBAPENEM ANTIBIOTICS PRECURSORS ACID AM1 M
  186759. 14390N
  186760. 2/28/96
  186761. A~A FACIALLY
  186762. SELECTIVE PROTONATION CONTROLS THE STEREOCHEMISTRY OF A KEY INTERMEDIATE IN THE SYNTHESIS OF 1-b
  186763. METHYL CARBAPENEMS
  186764. 1994 X    3749
  186765. 3751Y
  186766. 13382
  186767. HASSNER, A.
  186768. J. Het. Chem.M
  186769. 14391N
  186770. 2/28/96
  186771. ANSTEREOSELECTIVITY DURING CYCLOADDITIONS LEADING TO FUNCTIONALIZED HETEROCYCLES
  186772. 1994X
  186773. 13383
  186774. MARTIN, S. F.
  186775. J. Het. Chem.M
  186776. 14392N
  186777. 2/28/96
  186778. A=STRATEGIES FOR THE SYNTHESIS OF HETEROCYCLIC NATURAL PRODUCTS
  186779. 1994 X
  186780. 13384
  186781. GRONOWITZ, S.
  186782. J. Het. Chem.C
  186783. OXIDES 1ST SYNTHESIS NITRATION ORIENTATION DITHIENO<2,3
  186784. 3',2'
  186785. D>PYRIDINE PHENANTHRIDINE BROMINATION LITHIATION ANALOGS DITHIENO<3,4
  186786. 3',4'
  186787. D>PYRIDINE M
  186788. 14393N
  186789. 2/28/96
  186790. AdTHE VERSATILE CHEMISTRY OF THIOPHENES 
  186791.  THE EFFECTS OF B
  186792. SIDE CONTRA C
  186793. SIDE ANNELATION ON REACTIVITY
  186794. 13385
  186795. A    GRIGG, R.
  186796. J. Het. Chem.M
  186797. 14394N
  186798. 2/28/96
  186799. AjHETEROCYCLE SYNTHESIS BY PALLADIUM CATALYSED CYCLISATION
  186800. ANION CAPTURE PROCESSES 
  186801.  A POWERFUL NEW STRATEGY
  186802. 1994 X
  186803. 13386
  186804. PANDIT, U. K.
  186805. J. Het. Chem.C{NATURAL (+)
  186806. SESBANIMIDE
  186807. A ELLIPTICINE DERIVATIVES TRICYCLIC HEART SPONGE (
  186808. SESBANIMIDE
  186809. A INTERMEDIATE DRUMMONDII ANALOGS M
  186810. 14395N
  186811. 2/28/96
  186812. AWSYNTHETIC STRATEGIES DIRECTED TO THE ANTITUMOUR ALKALOIDS SESBANIMIDE
  186813. A AND MANZAMINE
  186814. 1994X
  186815. 13387
  186816. MURAOKA, O.
  186817. J.C.S. Perkin Trans. 1C
  186818. METHANE REARRANGEMENT GAMMA
  186819. BUTYROLACTONE HYDROXY ESTERS LACTONES PHOTOCHEMISTRY BUTENOLIDES ALKYLATION KETONES SYSTEM ROUTE M
  186820. 14396N
  186821. 2/28/96
  186822. AlFURAN
  186823. 2(3H)
  186824.  AND 2(5H)
  186825. ONES .5. PHOTOREACTIONS OF 3
  186826. BENZYLFURAN
  186827. 2(5H)
  186828. ONES;  CYCLISATION TO INDENO FURANONES
  186829. 1994X    1833
  186830. 1845Z
  186831. 13388
  186832. BHAT, L.
  186833. J.C.S. Perkin Trans. 1C
  186834. CLAISEN REARRANGEMENT M
  186835. 14397N
  186836. 2/28/96
  186837. AIREARRANGEMENT STUDIES ON ACYLKETENE O
  186838. YNYL S
  186839. METHYL MONOTHIOKETALS
  186840. 1994 X    1749
  186841. 1752Z
  186842. 13389
  186843. GABBUTT, C. D.
  186844. J.C.S. Perkin Trans. 1C&9
  186845. BORABICYCLO<3.3.1>NONANE REDUCTIONS M
  186846. 14398N
  186847. 2/28/96
  186848. A%ALLENES FROM 3
  186849. BROMO
  186850. BENZOPYRANS
  186851. 1994 X    1733
  186852. 1737Z
  186853. 13390
  186854. ADLINGTON, R. M.
  186855. J.C.S. Perkin Trans. 1CdORGANIC ELECTROPHILES ASYMMETRIC
  186856. SYNTHESIS ORGANOTIN REAGENTS PALLADIUM VINYL BUTYROLACTONES ESTERS M
  186857. 14399N
  186858. 2/28/96
  186859. A STUDY OF THE INTRAMOLECULAR STILLE CROSS COUPLING REACTION OF VINYLSTANNYL CHLOROFORMATES:  APPLICATION TO THE SYNTHESIS OF A
  186860. METHYLENE LACTONES
  186861. 1994X    1697
  186862. 1701Z
  186863. 13391
  186864. GOMEZ, A. M.
  186865. J.C.S. Perkin Trans. 1C
  186866. RESEMBLE GRANDFATHER GLUCOSE DIELS
  186867. ALDER REACTIONS 2,3
  186868. UNSATURATED SUGARS CYCLIZATION REACTION ORGANOTIN COMPOUNDS REAGENTS ACETYLENES PALLADIUM PROGENY ESTERS M
  186869. 14400N
  186870. 2/28/96
  186871. SOME STUDIES ON PROXIMAL ADDITION
  186872. ELIMINATION PROCEDURES IN INTERMOLECULAR CARBON
  186873. CARBON BOND
  186874. FORMING FREE RADICAL REACTIONS. CONVENIENT SYNTHESIS OF ETHYL (E)
  186875. (ETHYL 2,3,6,7,8
  186876. PENTADEOXY
  186877. ERYTHRO
  186878. DIENOPYRANOSID)
  186879. URONATE
  186880. 1994X    1689
  186881. 1695Z
  186882. 13392
  186883. GRAVESTOCK, M. B.
  186884. J.C.S. Perkin Trans. 1C-OXIME OLEFIN CYCLOADDITION ADDITIONS ANALOGS M
  186885. 14401N
  186886. 2/28/96
  186887. A[STEREOSELECTIVITY OF INTRAMOLECULAR CYCLISATIONS OF NITRONES DERIVED FROM 3
  186888. OXAHEPT
  186889. ENALS
  186890. 1994 X    1661
  186891. 1663Z
  186892. 13393
  186893. Lee, Y. S.B
  186894. HeterocyclesK
  186895. (VOL 37, PG 303, 1994)M
  186896. 14402N
  186897. 2/28/96
  186898. ArSTUDIES ON THE SITE
  186899. SELECTIVE N
  186900. ACYLIMINIUM ION CYCLIZATION 
  186901.  SYNTHESIS OF (+/
  186902. GLOCHIDINE AND (+/
  186903. GLOCHIDICINE
  186904. 1994 X
  186905. 2173Y
  186906. 13394
  186907. GRIMMETT,  M. R.
  186908. HeterocyclesC
  186909. CARBON
  186910. DIOXIDE SIMULTANEOUS PROTECTION ALTERNATIVE LOCATIONS ELECTROPHILIC ATTACK NUCLEOPHILIC CENTERS N
  186911. OXIDES ACTIVATION REAGENT IMIDAZOLES CARBODESILYLATION M
  186912. 14403N
  186913. 2/28/96
  186914. AgSYNTHESIS AND REACTIONS OF LITHIATED MONOCYCLIC AZOLES CONTAINING two OR MORE HETEROATOMS .3. PYRAZOLES
  186915. 1994 X    2087
  186916. 2147Y
  186917. 13395
  186918. KORBONITS, D.
  186919. HeterocyclesC
  186920. CHAIN TAUTOMERISM GENERAL
  186921. METHOD 1,2,4
  186922. OXADIAZOLES TRANSFORMATION 4
  186923. AMINOPYRIMIDINES REARRANGEMENTS DERIVATIVES 3
  186924. OXIDES SYSTEM M
  186925. 14404N
  186926. 2/28/96
  186927. A0SYNTHESIS OF HETEROCYCLES FROM AMINOAMIDE OXIMES
  186928. 1994 X    2051
  186929. 2068Y
  186930. 13396
  186931. A    MCNAB, H.
  186932. HeterocyclesC[PYRROLIZIDINE ALKALOIDS TERPENE DERIVATIVES SENECIO CONSTITUENTS FUROEREMOPHILANES ANALOGS M
  186933. 14405N
  186934. 2/28/96V
  186935. PYRROLIZIN
  186936. ONESW
  186937. 1994X    1977
  186938. 2008Y
  186939. 13397
  186940. BALASUBRAMANIAN, M.
  186941. HeterocyclesC
  186942. ALKOXIDE
  186943. INDUCED REACTION PHASE
  186944. TRANSFER CATALYSIS CARBONYL
  186945. COMPOUNDS REGIOSPECIFIC SYNTHESIS ANTIFUNGAL AGENTS ALKYL
  186946. HALIDES ALDEHYDES KETONES SERIES M
  186947. 14406N
  186948. 2/28/96
  186949. A<APPROACHES TO THE SYNTHESIS OF 1
  186950. SUBSTITUTED 1,2,4
  186951. TRIAZOLES
  186952. 1994 X    1951
  186953. 1975Y
  186954. 13398
  186955. HUDSON, R. F.
  186956. HeterocyclesC+MOLECULAR
  186957. CRYSTALS REVISION CONTACTS RADII M
  186958. 14407N
  186959. 2/28/96
  186960. AeSHORT INTERACTIONS BETWEEN HETEROCYCLIC SULFUR ATOMS AND THIOCARBONYL SULFUR OR CARBONYL OXYGEN ATOMS
  186961. 1994 X    1933
  186962. 1950Y
  186963. 13399
  186964. JOHNSON, A. P.
  186965. HeterocyclesC'N
  186966. SUBSTITUTED BENZOTRIAZOLES CHEMISTRY M
  186967. 14408N
  186968. 2/28/96
  186969. AMPREPARATION AND PHOTOLYSIS OF 1
  186970. HETEROSUBSTITUTED 1
  186971. ALKENYL)BENZOTRIAZOLES
  186972. 1994X    1913
  186973. 1932Y
  186974. 13400
  186975. FROHLICH, J.
  186976. HeterocyclesC
  186977. NITRILES KETONES M
  186978. 14409N
  186979. 2/28/96
  186980. A6A NOVEL SYNTHESIS OF 3,3
  186981. (SPIRO)SUBSTITUTED AZETIDINES
  186982. 1994X    1879
  186983. 1891Y
  186984. 13401
  186985. SCHANTL, J. G.
  186986. HeterocyclesM
  186987. 14410N
  186988. 2/28/96
  186989. ARYLAMINO
  186990. DIHYDRO
  186991. IMIDAZOLE
  186992. THIONES FROM THE REACTION OF 1
  186993. ARYLHYDRAZONO)ALKYL]
  186994. PYRIDINIUMIODIDES WITH POTASSIUM THIOCYANATE
  186995. 1994X    1873
  186996. 1878Y
  186997. 13402
  186998. AGER, D. J.
  186999. HeterocyclesCcDIELS
  187000. ALDER REACTION ORGANIC
  187001. SYNTHESIS LITHIUM ENOLATE HIGH
  187002. PRESSURE FURAN HYDROXYLATION ADDITIONS M
  187003. 14411N
  187004. 2/28/96
  187005. DEVELOPMENT OF METHODOLOGY BASED ON THE USE OF THE 7
  187006. OXABICYCLO[2.2.1]HEPTANYL SYSTEM FOR THE PREPARATION OF CARBOHYDRATE DERIVATIVES
  187007. 1994 X    1789
  187008. 1805Y
  187009. 13403
  187010. CURRAN, D. P.
  187011. Heterocycles
  187012. C_ASYMMETRIC THERMAL
  187013. REACTIONS ANNULATION REACTIONS CHIRAL AUXILIARY INDUCTION ESTERS ACID SCOPE M
  187014. 14412N
  187015. 2/28/96
  187016. AfCONTROLLING STEREOCHEMISTRY IN RADICAL ADDITION AND CYCLIZATION REACTIONS WITH OPPOLZER CAMPHOR SULTAM
  187017. 1994 X    1773
  187018. 1788Y
  187019. 13404
  187020. A    ZHENG, Q.
  187021. HeterocyclesC ARYLBORONIC ACIDS BORONIC ACIDS M
  187022. 14413N
  187023. 2/28/96
  187024. AJVINYLATION OF THE INDOLE 3
  187025. POSITION VIA PALLADIUM
  187026. CATALYZED CROSS
  187027. COUPLING
  187028. 1994X    1761
  187029. 1772Y
  187030. 13405
  187031. BOHN, B.
  187032. HeterocyclesC
  187033. SUBSTITUTION M
  187034. 14414N
  187035. 2/28/96
  187036. AEHAMMICK CYCLIZATIONS STUDIES ON THE MECHANISM OF THE HAMMICK REACTION
  187037. 1994 X    1731
  187038. 1746Y
  187039. 13406
  187040. BURGER, K.
  187041. HeterocyclesC
  187042. HETEROCYCLIC
  187043. COMPOUNDS M
  187044. 14415N
  187045. 2/28/96
  187046. AUXILIARY
  187047. CONTROLLED SITE SELECTIVITY [4+2] CYCLOADDITION REACTIONS OF A,b
  187048. UNSATURATED CARBONYL COMPOUNDS TO 4,4
  187049. (TRIFLUOROMETHYL)
  187050. SUBSTITUTED HETERO
  187051. DIENES
  187052. 1994 X    1719
  187053. 1729Y
  187054. 13407
  187055. TANYELI, C.
  187056. HeterocyclesCMEFFICIENT SYNTHESIS 2H
  187057. PYRAN
  187058. ONE DERIVATIVES CARDIOACTIVE STEROIDS BUFALIN M
  187059. 14416N
  187060. 2/28/96
  187061. A0ACID CATALYZED A
  187062. PYRONE RING FORMATION REACTIONS
  187063. 1994X    1705
  187064. 1715Y
  187065. 13408
  187066. KRUTOSIKOVA, A.
  187067. HeterocyclesC(FURAN
  187068. DERIVATIVES THIENO<3,2
  187069. C>PYRIDINE M
  187070. 14417N
  187071. 2/28/96
  187072. ApSUBSTITUTED VINYL AZIDES IN SYNTHESIS OF FURO[3,2
  187073. B]DIPYRROLES AND PYRROLO[2',3'/4,5] FURO[3,2
  187074. C]PYRIDINES
  187075. 1994 X    1695
  187076. 1700Y
  187077. 13409
  187078. CASASCHI, A.
  187079. HeterocyclesC=X=Y
  187080. ZH COMPOUNDS POTENTIAL 1,3
  187081. DIPOLES AMINO
  187082. ACIDS NINHYDRIN M
  187083. 14418N
  187084. 2/28/96
  187085. THE REACTION OF ISATIN AZOMETHINE YLIDES WITH (Z)
  187086. OXOINDOLIN
  187087. 3-YLIDENE AND (E)
  187088. OXOINDOLIN
  187089. YLIDENE ACETOPHENONES 
  187090.  CONCERTED VS APPARENT NON
  187091. CONCERTED 1,3
  187092. DIPOLAR CYCLOADDITION
  187093. 1994 X    1673
  187094. 1686Y
  187095. 13410
  187096. KANEKO, K.
  187097. HeterocyclesCbPYRAZOLO<1,5
  187098. A>INDOLE DERIVATIVES INFRARED
  187099. SPECTROSCOPY MITSUNOBU REACTION MECHANISM AGENTS ACIDS M
  187100. 14419N
  187101. 2/28/96
  187102. AgPREPARATION OF 2
  187103. DIHYDRO
  187104. [1,3,4]OXADIAZINO[4,5
  187105. A]INDOLES AS A [A]
  187106. FUSED INDOLE DERIVATIVES
  187107. 1994X    1645
  187108. 1656Y
  187109. 13411
  187110. KAPPE, C. O.
  187111. HeterocyclesM
  187112. 14420N
  187113. 2/28/96
  187114. AeSYNTHESIS AND FLASH VACUUM PYROLYSIS OF ISOXAZOLO[5,4
  187115. D]PYRIMIDINES AND ISOTHIAZOLO[5,4
  187116. D]PYRIMIDINES
  187117. 1994X    1615
  187118. 1622Y
  187119. 13412
  187120. KOTALI, A.
  187121. HeterocyclesC4PHENOLIC HYDROXYL TETRAACETATE REPLACEMENT CARBONYL 
  187122. 14421N
  187123. 2/28/96
  187124. AYOXIDATION OF N
  187125. ACYL HYDRAZONES OF O
  187126. AMINOARYL KETONES 
  187127.  SYNTHESIS OF 2
  187128. ACYLAMINOINDAZOLES
  187129. 1994X    1541
  187130. 1548Y
  187131. 13413
  187132. MISICVUKOVIC, M.
  187133. HeterocyclesM
  187134. 14422N
  187135. 2/28/96
  187136. TRANSMISSION OF ELECTRONIC EFFECTS THROUGH THE VINYL GROUP
  187137.  REACTIVITIES OF THE (E)
  187138. SUBSTITUTED PHENYL
  187139. PYRIDINE
  187140. ACRYLIC ACIDS
  187141. 1994X    1503
  187142. 1510Y
  187143. 13414
  187144. LINGIBE, O.
  187145. HeterocyclesC
  187146. ALCOHOLS LACTAMS ESTERS M
  187147. 14423N
  187148. 2/28/96
  187149. AcASYMMETRIC SYNTHESIS WITH CHIRAL HYDROGENOLYSABLE AMINES 
  187150.  A NEW ROUTE TO ENANTIOPURE ETHANOLAMINES
  187151. 1994 X    1469
  187152. 1472Y
  187153. 13415
  187154. A    KONDO, Y.
  187155. HeterocyclesM
  187156. 14424N
  187157. 2/28/96
  187158. AAREDUCTIVE LITHIATION OF HALOPYRIDINES USING LITHIUM NAPHTHALENIDE
  187159. 1994X    1467
  187160. 1468Y
  187161. 13416
  187162. ABRAMOVITCH, R. A.
  187163. HeterocyclesC
  187164. ARYLNITRENIUM IONS ACIDM
  187165. 14425N
  187166. 2/28/96
  187167. AhPHOTOLYTIC GENERATION OF N
  187168. ACYLNITRENIUM IONS UNDER NEUTRAL CONDITIONS 
  187169.  SYNTHESIS OF POLYCYCLIC LACTAMS
  187170. 1994X    1463
  187171. 1466Y
  187172. 13417
  187173. DUFOUR, B.
  187174. HeterocyclesC44
  187175. PI PARTICIPATION 1
  187176. BUTADIENES 1
  187177. AZADIENES M
  187178. 14426N
  187179. 2/28/96
  187180. A\A STUDY OF THE HETERO
  187181. DIELS
  187182. ALDER REACTION OF N
  187183. ALKYL
  187184. CYANO
  187185. AZADIENES WITH 2
  187186. VINYLINDOLE
  187187. 1994 X    1455
  187188. 1458Y
  187189. 13418
  187190. SHANKAR, R.
  187191. HeterocyclesC
  187192. CONVENIENT SYNTHESIS ESTERS M
  187193. 14427N
  187194. 2/28/96
  187195. SYNTHESIS OF CHIRAL LACTAMS AS TEMPLATES FOR ENZYME INHIBITORS 
  187196.  AN UNUSUAL ANNULATION IN THE INTRAMOLECULAR WADSWORTH
  187197. HORNER
  187198. EMMONS REACTION
  187199. 1994 X    1451
  187200. 1454Y
  187201. 13419
  187202. DONDONI, A.
  187203. J.C.S. Chem. Commun.C
  187204. ALPHA
  187205. AMINO ALDEHYDES D
  187206. ERYTHRO
  187207. SPHINGOSINE D
  187208. THREO
  187209. SPHINGOSINE STEREOCONTROLLED ADDITION ORGANIC
  187210. SYNTHESIS VICINAL DIAMINES 1,2
  187211. DIAMINES DERIVATIVES ATTACK ACIDS M
  187212. 14428N
  187213. 2/28/96
  187214. TUNABLE STEREOSELECTIVITY IN THE ADDITION OF 2
  187215. LITHIOTHIAZOLE TO L
  187216. SERINAL DERIVED N
  187217. BENZYL NITRONE. SYNTHESIS OF C
  187218. 2 EPIMER 2,3
  187219. DIAMINO
  187220. HYDROXYBUTANALS
  187221. 1994X    1731
  187222. 1733Z
  187223. 13420
  187224. DEVERY, M. P.
  187225. J.C.S. Chem. Commun.M
  187226. 14429N
  187227. 2/28/96
  187228. AOTHE UNUSUAL STEVENS TYPE REARRANGEMENTS OF SOME DIALKYLSULFIDES ON A RH
  187229. RH BOND
  187230. 1994X    1721
  187231. 1722Z
  187232. 13421
  187233. SUAREZ, D.
  187234. J.C.S. Chem. Commun.CYTRANSITION STRUCTURES REACTIVITY CATALYSIS ABINITIO STEREOSELECTIVITY MECHANISM ETHYLENE M
  187235. 14430N
  187236. 2/28/96
  187237. AQSOLVENT EFFECTS ON HETERO DIELS
  187238. ALDER REACTIONS OF SULFUR DIOXIDE WITH 1,3
  187239. DIENES
  187240. 1994 X    1683
  187241. 1684Z
  187242. 13422
  187243. DUETSCH, M.
  187244. DE MEIJEREB
  187245. J.C.S. Chem. Commun.C
  187246. CHROMIUM CARBENE COMPLEXES ALKYNES LIGANDS ANNULATION SKELETON 
  187247.  CHROMIUM COMPLEX FISCHER CARBENE CYCLOADDITION AMINE ALKYNE MECHANISM ORGANOMETALLICM
  187248. 14431N
  187249. 2/28/96
  187250. METHYLENE
  187251. CYCLOPENTENONES AS NEW FORMAL [2+2+1] CYCLOADDUCTS FROM [2
  187252. (DIBENZYLAMINO)ETHENYL] CARBENE CHROMIUM COMPLEXES AND ALKYNES
  187253. 1994 X    1679
  187254. 1680Z
  187255. 13423
  187256. NEMOTO, H.
  187257. J.C.S. Chem. Commun.C
  187258. ALDOL M
  187259. 14432N
  187260. 2/28/96
  187261. AMPALLADIUM CATALYSED ADDITION OF MASKED FORMYL CYANIDES ROCH(CN)2 TO ALDEHYDES
  187262. 1994 X    1665
  187263. 1666Z
  187264. 13424
  187265. AGGARWAL, V. K.
  187266. J.C.S. Chem. Commun.CUASYMMETRIC
  187267. SYNTHESIS THIOL ESTERS AMINO
  187268. ACIDS LEWIS ACID ALDEHYDES DIPEPTIDE CYANIDE M
  187269. 14433N
  187270. 2/28/96
  187271. TRANS
  187272. DITHIANE
  187273. DIOXIDE, A NEW CHIRAL ACYL ANION EQUIVALENT FOR THE PREPARATION OF MASKED ACTIVATED ACIDS: APPLICATION TO THE SYNTHESIS OF A
  187274. HYDROXY ACID DERIVATIVES
  187275. 1994X    1653
  187276. 1654Z
  187277. 13425
  187278. BARLUENGA, J.
  187279. JACSM
  187280. 14434N
  187281. 2/28/96
  187282. ASYMMETRIC EXO
  187283. SELECTIVE DIELS
  187284. ALDER REACTIONS OF CYCLIC BF2 ADDUCTS OF FUNCTIONALIZED FISCHER VINYLCARBENE COMPLEXES WITH CHIRAL 2
  187285. AMINO
  187286. DIENES
  187287. 1994X    6949
  187288. 6950Y
  187289. 13426
  187290. KUZMICH, D.
  187291. JACSM
  187292. 14435N
  187293. 2/28/96
  187294. A%TOTAL SYNTHESIS OF DL
  187295. OXOGELSEMINE
  187296. 1994 X    6943
  187297. 6944Y
  187298. 13427
  187299. CHANG, S. B.
  187300. JACSM
  187301. 14436N
  187302. 2/28/96
  187303. EFFECT OF CHIRAL QUATERNARY AMMONIUM SALTS ON (SALEN)MN
  187304. CATALYZED EPOXIDATION OF CIS
  187305. OLEFINS. A HIGHLY ENANTIOSELECTIVE, CATALYTIC ROUTE TO TRANS
  187306. EPOXIDES
  187307. 1994X    6937
  187308. 6938Y
  187309. 13428
  187310. HARVEY, D. F.
  187311. 1DIELS
  187312. ALDER REACTION ELECTRON
  187313. POOR OLEFINS PRODUCT DISTRIBUTION ORGANIC
  187314. SYNTHESIS CYCLOADDITION TETHER LENGTH ALKYNES ENYNES ACETYLENES CYCLOPROPANATION 
  187315. INTRODUCTION CARBENOID CHROMIUM CARBENE COMPLEX WRITING INSERTION CARBON MONOXIDE QUINONE MECHANISM ALKYNE VINYL KETENE INTRAMOLECULAR CYCLOPROPANATION
  187316. 14437N
  187317. 2/28/96
  187318. AgEFFECT OF ALKENE SUBSTITUENTS ON MOLYBDENUM AND CHROMIUM CARBENE COMPLEX MEDIATED CYCLIZATION REACTIONS
  187319. 1994 X    6719
  187320. 6732Y
  187321. 13429
  187322. PORTER, N. A.
  187323. JACSCbLINOLEATE HYDROPEROXIDES ALLYLIC HYDROPEROXIDES VISCOSITY DEPENDENCE CAGE RETURN HOMOLYSIS OXYGEN M
  187324. 14438N
  187325. 2/28/96
  187326. THE MECHANISM OF THE [3,2] ALLYLPEROXYL REARRANGEMENT:  A RADICAL
  187327. DIOXYGEN PAIR REACTION THAT PROCEEDS WITH STEREOCHEMICAL MEMORY
  187328. 1994 X    6697
  187329. 6705Y
  187330. 13430
  187331. PORTER, N. A.
  187332. JACSC
  187333. TEMPERATURE AUTOXIDATION ELECTRON
  187334. SPIN RESONANCE UNSATURATED FATTY
  187335. ACIDS ALLYLIC HYDROPEROXIDES RATE CONSTANTS HYDROGEN
  187336. ATOM STEREOCHEMISTRY ALKENES M
  187337. 14439N
  187338. 2/28/96
  187339. AcA MECHANISTIC STUDY OF OLEATE AUTOXIDATION:  COMPETING PEROXYL H
  187340. ATOM ABSTRACTION AND REARRANGEMENT
  187341. 1994X    6690
  187342. 6696Y
  187343. 13431
  187344. CARREIRA, E. M.
  187345. GALPHA,BETA
  187346. UNSATURATED KETONES PHOTOCHEMICAL CYCLOADDITION CONJUGATED CYCLOHEXENONES 2+2 PHOTOCYCLOADDITION ELECTRONIC CONTROL ALLENE STEREOSELECTIVITY PHOTOADDITION REDUCTION STEREOCHEMISTRY 
  187347. PHOTOCHEM INTRAMOLECULAR ALLENE 2+2 CHIRAL ASYMMETRIC INDUCTION ENONE INTRODUCTION CYCLOADDITION PHOTOCYCLOADDITION ENANTIOSELECTIVITY
  187348. 14440N
  187349. 2/28/96
  187350. AuASYMMETRIC INDUCTION IN INTRAMOLECULAR [2+2]
  187351. PHOTOCYCLOADDITIONS OF 1,3
  187352. DISUBSTITUTED ALLENES WITH ENONES AND ENOATES
  187353. 1994X    6622
  187354. 6630Y
  187355. 13432
  187356. KOPACH, M. E.
  187357. ARENE
  187358. METAL
  187359. COMPLEXES ETA
  187360. COORDINATED ARENES NUCLEOPHILIC
  187361. ADDITION SELECTIVE HYDROGENATION CRYSTAL
  187362. STRUCTURE PI
  187363. HYDROCARBONS PENTAAMMINEOSMIUM(II) DEAROMATIZATION SYNTHONS BENZENE M
  187364. 14441N
  187365. 2/28/96
  187366. NOVEL MICHAEL ADDITIONS TO PHENOLS PROMOTED BY OSMIUM(II): CONVENIENT STEREOSELECTIVE SYNTHESES OF 2,4
  187367.  AND 2,5
  187368. CYCLOHEXADIENONES
  187369. 1994X    6581
  187370. 6592Y
  187371. 13433
  187372. BAILEY, W. F.
  187373. JACSC
  187374. TANDEM ANIONIC CYCLIZATION RADICAL CHAIN REACTIONS ORGANIC
  187375. SYNTHESIS EXCHANGE CARBON BUTYLLITHIUM BOND BICYCLO<2.2.1>HEPTANES 5
  187376. HEXEN
  187377. YLLITHIUM STEREOSELECTIVITY M
  187378. 14442N
  187379. 2/28/96
  187380. Am''SUPER BASES'' DERIVED FROM 5
  187381. HEXENYLLITHIUM AND ALKALI METAL ALKOXIDES:  REARRANGEMENTS OF 5
  187382. HEXENYLALKALIS
  187383. 1994 X    6577
  187384. 6580Y
  187385. 13434
  187386. ILAVSKY, D.
  187387. Coll. Czech. Chem. Commun.M
  187388. 14443N
  187389. 2/28/96
  187390. A4SYNTHESIS OF NEW 2
  187391. SUBSTITUTED 4
  187392. FURYL)
  187393. PYRANS
  187394. 1994 X    1458
  187395. 1462Y
  187396. 13435
  187397. GRELIERMARLY, M. C.
  187398. Can. J. Chem.C
  187399. POLARIZATION TRANSFER ENHANCEMENT SELECTIVE
  187400. POPULATION INVERSION INDUCED RING ENLARGEMENT STEREOCHEMICAL COURSE SPECTROSCOPY BICYCLO<N.1.0>ALKYLSILANES MOLECULES KETONES SPECTRA SCOPE M
  187401. 14444N
  187402. 2/28/96
  187403. AwREARRANGEMENT IN TRICYCLIC SERIES 
  187404.  SYNTHESIS AND REACTIVITY OF BIS
  187405. TRIMETHYLSILYL
  187406. BICYCLO [N,1,0] 2
  187407. ALKENE ANTI OXIDES
  187408. 1994 X    1541
  187409. 1547Y
  187410. 13436
  187411. A    FATHI, T.
  187412. Can. J. Chem.CcCYCLOADDITION REGIOCHEMISTRY DIARYL NITRILIMINES STEREOCHEMISTRY DIPHENYLNITRILIMINE CYCLOADDITION M
  187413. 14445N
  187414. 2/28/96
  187415. REACTIVITY OF ARYLIDENE BENZOTHIAZINONE DIOXIDES IN [3+2]
  187416. CYCLOADDITIONS 
  187417.  COMPETITION BETWEEN DIPOLAROPHILIC SITES 
  187418.  FORMATION OF CYCLOADDUCTS
  187419. 1994X    1424
  187420. 1428Y
  187421. 13437
  187422. LAKHLIFI, T.
  187423. Can. J. Chem.CHDIPHENYLNITRILIMINE STEREOCHEMISTRY REGIOCHEMISTRY REACTIVITY ADDITIONS M
  187424. 14446N
  187425. 2/28/96
  187426. AaDOUBLE DIASTEREOSELECTIVITY OF 1,3
  187427. DIPOLAR CYCLOADDITIONS OF SUBSTITUTED CYCLIC AZOMETHINE YLIDES
  187428. 1994 X    1417
  187429. 1423Y
  187430. 13438
  187431. SAKURAGI, H.
  187432. Bull. Chem. Soc. Jpn.CyMETHOXY PHENYLALKENYL PHENANTHRENE CARBOXYLATES PHOTOCHEMICAL CYCLOADDITION PHOTOPHYSICAL BEHAVIOR BENZONITRILE PATHWAYS M
  187433. 14447N
  187434. 2/28/96
  187435. INTRAMOLECULAR PHOTOCYCLOADDITION OF THE C=C DOUBLE BOND TO THE C EQUIVALENT to N TRIPLE BOND RESULTING IN THE FORMATION OF A NOVEL CYCLIC SYSTEM
  187436. 1994 X    1769
  187437. 1772Y
  187438. 13439
  187439. NISHIYAMA, T.
  187440. Bull. Chem. Soc. Jpn.C
  187441. DERIVATIVES M
  187442. 14448N
  187443. 2/28/96
  187444. AzONE
  187445. POT SYNTHESIS OF ETHYL 3
  187446. HYDROXYALKYL)AMINOALKANOATES BY RING OPENING OF 1,3
  187447. OXAZOLIDINES USING REFORMATSKY REAGENT
  187448. 1994 X    1765
  187449. 1768Y
  187450. 13440
  187451. YAMAGUCHI, M.
  187452. Bull. Chem. Soc. Jpn.C;SOLID
  187453. STATE POLYMERIZATION POLYYNES DIACETYLENES L
  187454. 660,631 M
  187455. 14449N
  187456. 2/28/96
  187457. AuSYNTHESIS AND REACTIONS OF MONOSILYLATED 1,3,5
  187458. HEXATRIYNE AND 1,3,5,7
  187459. OCTATETRAYNE 
  187460.  TOTAL SYNTHESIS OF CARYOYNENCINS
  187461. 1994 X    1717
  187462. 1725Y
  187463. 13441
  187464. MUKAIYAMA, T.
  187465. Bull. Chem. Soc. Jpn.C
  187466. SILYL ENOL ETHERS COORDINATED TIN(II) TRIFLATE CHIRAL PROMOTER LEWIS ACID SYN
  187467. ALPHA ALDEHYDES THIOESTERS OLEFINS COMPLEX ACETALS M
  187468. 14450N
  187469. 2/28/96
  187470. AwDIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF SYN
  187471. DIOL AND ANTI
  187472. DIOL UNITS BY ASYMMETRIC ALDOL REACTIONS
  187473. 1994 X    1708
  187474. 1716Y
  187475. 13442
  187476. MATSUMOTO, K.
  187477. Bull. Chem. Soc. Jpn.
  187478. CLLITHIUM CARBENOIDS ORGANIC
  187479. SYNTHESIS SILACYCLOBUTANE VINYLSILANES ALDEHYDES M
  187480. 14451N
  187481. 2/28/96
  187482. GENERATION OF 2
  187483. LITHIO
  187484. (TRIMETHYLSILYL)SILACYCLOPENTANE AND 2
  187485. LITHIO
  187486. (PHENYLTHIO)SILACYCLOPENTANE AND THEIR USE FOR THE SYNTHESIS OF 1,4
  187487. BUTANEDIOLS AND g
  187488. HYDROXYKETONES
  187489. 1994X    1694
  187490. 1700Y
  187491. 13443
  187492. MURATA, S.
  187493. Bull. Chem. Soc. Jpn.
  187494. CwENOL SILYL ETHERS BENZENESELENENYL TRIFLATE TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE CYCLIZATION OXIRANES ACETALS ACID M
  187495. 14452N
  187496. 2/28/96
  187497. A{PRACTICAL SYNTHESIS OF PALLADIUM BIS(TRIFLUOROMETHANESULFONATE) AND ITS APPLICATION to THE SYNTHESIS OF PALLADIUM COMPLEXES
  187498. 1994X    1746
  187499. 1748Y
  187500. 13444
  187501. OTTE, A. R.
  187502. Angew. Chem. Int. Ed. Engl. M
  187503. 14453N
  187504. 2/28/96
  187505. CYCLOPROPANES BY NUCLEOPHILIC ATTACK OF MONO
  187506.  AND DIARYL
  187507. SUBSTITUTED (h3
  187508. ALLYL)PALLADIUM COMPLEXES:  ARYL EFFECT AND STEREOCHEMISTRY
  187509. 1994X    1280
  187510. 1282Y
  187511. 13445
  187512. GLEITER, R.
  187513. Angew. Chem. Int. Ed. Engl. M
  187514. 14454N
  187515. 2/28/96
  187516. A8NEW TYPES OF METAL
  187517. STABILIZED CYCLOBUTADIENE SUPERPHANES
  187518. 1994X    1272
  187519. 1274Y
  187520. 13446
  187521. GLEITER, R.
  187522. Angew. Chem. Int. Ed. Engl. M
  187523. 14455N
  187524. 2/28/96
  187525. A7EFFICIENT SYNTHESIS OF HETERORADIALENES BY SN' REACTION
  187526. 1994 X    1270
  187527. 1272Y
  187528. 13447
  187529. KUBAS, G. J.
  187530. Acc. Chem. Res.M
  187531. 14456N
  187532. 2/28/96
  187533. A_CHEMICAL TRANSFORMATIONS AND DISPROPORTIONATION OF SULFUR DIOXIDE ON TRANSITION METAL COMPLEXES
  187534. 1994 X
  187535. 13448
  187536. HODGETTS, K. J.
  187537. Tet. Lett.K
  187538. THE ADDITIONS OF VARIOUS ORGANOMETALLIC SPECIES TO 3
  187539. OXABICYCLO[3.2.0]HEPT
  187540. OL ARE DIASTEREOSELECTIVE; THE RESULTS ARE CONSISTENT WITH ADDITION TO THE LESS HINDERED FACE OF A METAL
  187541. CHELATED FORM OF THE CORRESPONDING GAMMA
  187542. HYDROXYALDEHYDE.M
  187543. 14457N
  187544. 2/28/96
  187545. THE ADDITION OF ORGANOMETALLIC REAGENTS to 3
  187546. OXABICYCLO[3.2.0]HEPT
  187547. OL:  A STEREOSELECTIVE ROUTE to 6
  187548. OXYGENATED (2Z,4E)
  187549. ALKADIENALS
  187550. 1994X    4645
  187551. 4648Y
  187552. 13449
  187553. TANNER, D.
  187554. Tet. Lett.
  187555. CHIRAL LIGANDS ASYMMETRIC DIHYDROXYLATION CATALYTIC ASYMMETRIC ALLYLIC SUBSTITUTION CATALYTIC ASYMMETRIC CYCLOPROPANATION CATALYTIC ASYMMETRIC AZIRIDINATION COPPER
  187556.  COMPLEXES DIAZO
  187557. COMPOUNDS OLEFINS CATALYSIS DIHYDROXYLATION K
  187558. THE READILY AVAILABLE C
  187559. SYMMETRIC BIS(AZIRIDINES) I CAN ACT AS LIGANDS IN A VARIETY OF ASYMMETRIC TRANSFORMATIONS MEDIATED BY TRANSITION METALS IN THE BEST CASES, > 95% EECAN BE OBTAINED.M
  187560. 14458N
  187561. 2/28/96
  187562. SYMMETRIC BIS(AZIRIDINES): PP  A NEW CLASS OF CHIRAL LIGANDS FOR TRANSITION METAL
  187563. MEDIATED ASYMMETRIC SYNTHESIS
  187564. 1994X    4631
  187565. 4634Y
  187566. 13450
  187567. GENNARI, C.
  187568. Tet. Lett.C8DIASTEREOFACIAL SELECTIVITY ASYMMETRIC
  187569. SYNTHESIS DESIGN 
  187570. BORON ENOLATES BEARING MENTHONE
  187571. DERIVED CHIRAL LIGANDS ARECAPABLE OF FAIR TO EXCELLENT DIASTEREOCONTROL IN THEIR REACTIONS WITH CHIRAL ALDEHYDES. THIOESTER
  187572.  DERIVED (BETTER THAN KETONE DERIVED) ENOLATES ARE ABLE TO CONTROL ALDOL STEREOCHEMISTRY IRRESPECTIVE OF THE ALDEHYDE PREFERENCES.
  187573. 14459N
  187574. 2/28/96
  187575. A]REAGENT CONTROL IN THE ALDOL ADDITION REACTION OF CHIRAL BORON ENOLATES WITH CHIRAL ALDEHYDES
  187576. 1994 X    4623
  187577. 4626Y
  187578. 13451
  187579. BAMBINO, F.
  187580. Tet. Lett.C
  187581. CHIRAL ALPHA 
  187582. ?THE SOLID PHASE SYNTHESIS OF PEPTIDES INCORPORATING THESTERICALLY HINDERED ALPHA,ALPHA
  187583. DIALKYL AMINO ACIDSAMINOISOBUTYRIC ACID (AIB) AND ALPHA
  187584. METHYLSERINE (ALPHA
  187585. MESER) IS REPORTED. THESE AMINO ACIDS WERE INCORPORATED AS DIPEPTIDE UNITS EMPLOYING STANDARD COUPLING REAGENTS AND PEPTIDES WERE OBTAINED WITH HIGH PURITY.
  187586. 14460N
  187587. 2/28/96
  187588. A8SYNTHESIS OF PEPTIDES CONTAINING A,A-DIALKYL AMINOACIDS.
  187589. 1994 X    4615
  187590. 4618Y
  187591. 13452
  187592. IWAMURA, T.
  187593. Tet. Lett.
  187594. }REACTION OF THIAZOLO[3,2
  187595. 6][1,2,4]TRIAZOLIUM N
  187596. PHENACYLIDES 3 WITH DIMETHYL ACETYLENE DICARBOXYLATE  GAVE NOVEL COMPOUNDS, 2
  187597. PYRROLO[2,1
  187598. 1,2,4
  187599.  TRIAZOLYL) ETHENYL THIOBENZOATES 4 AND 2
  187600. PYRROLO[2,1
  187601. 1,2,4
  187602. TRIAZOLYL) ETHENYLTHIO] PROPENOATES 5. THE FORMER PRODUCTS 4 WOULD BE FORMED VIA A NEW TYPE OFINTRAMOLECULAR BENZOYL MIGRATION OF THE INTERMEDIARY 1: 1ADDUCTS 6.
  187603. 14461N
  187604. 2/28/96
  187605. NOVEL BENZOYL MIGRATION OF THE INTERMEDIARY 1: 1 ADDUCTS OF DIPOLAR CYCLOADDITION OF THIAZOLO[3,2
  187606. B][1,2,4]TRIAZOLIUM N
  187607. PHENACYLIDES WITH DIMETHYL ACETYLENEDICARBOXYLATE
  187608. 1994 X    4587
  187609. 4590Y
  187610. 13453
  187611. A    OKUDA, M.
  187612. Tet. Lett.C    ALCOHOLS 
  187613. COMBINATION OF THE NEIGHBORING AMINO GROUP PARTICIPATING MITSUNOBU REACTION AND CYCLIC SULPHAMIDATE PROCEDURE PROVIDED EFFICIENT STEREO
  187614.  AND REGIOSELECTIVE SYNTHESIS OFCHIRAL AMINO ETHER LIGANDS FOR ASYMMETRIC REACTIONS.M
  187615. 14462N
  187616. 2/28/96
  187617. STEREO
  187618.  AND REGIOCHEMICAL ASPECTS OF THE MITSUNOBU REACTION IN SYNTHESIS OF CHIRAL AMINO ETHER LIGANDS FOR ASYMMETRIC REACTIONS
  187619. 1994 X    4585
  187620. 4586Y
  187621. 13454
  187622. ARIMOTO, H.
  187623. Tet. Lett.C5CONTAINING NATURAL
  187624. PRODUCTS POLYPROPIONATE FRAGMENTS 
  187625. THE STRUCTURAL REVISION OF THE PRODUCT OF THE TANDEM ALDOL
  187626.  SWERN OXIDATION PROCESS TO BETA
  187627. TRIKETONES IS REPORTED. FURTHER OXIDATION OF PRODUCTS LEADING TO THE CORRESPONDING DIKETONES (EX. 4, 5) WAS OBSERVED. THE PROPERTIES OF THE BETA
  187628. TRIKETONE ARE ALSO DESCRIBED.
  187629. 14463N
  187630. 2/28/96
  187631. AVCHEMICAL PROPERTIES OF b
  187632. TRIKETONES:  REEXAMINATION OF ALBIZATI'S TANDEM ALDOL PROCESS
  187633. 1994 X    4581
  187634. 4584Y
  187635. 13455
  187636. KAMEYAMA, A.
  187637. Tet. Lett.CSRING
  187638. OPENING REACTION THIIRANES CARBOXYLIC ACID DERIVATIVES QUATERNARY ONIUM SALTS 
  187639. SNEW RING
  187640. OPENING REACTION OF THIIRANES WITH CARBOXYLIC ACID DERIVATIVES HAVING GOOD LEAVING GROUPS WASINVESTIGATED. THE REACTION OF THIIRANES WITH ACYLCHLORIDES OR S
  187641. ARYL THIOESTERS USING QUATERNARY ONIUM SALTS AS NEUTRAL CATALYSTS PROCEEDED VERY SMOOTHLY AND REGIOSELECTIVELY TO AFFORD THE CORRESPONDING S
  187642. THIOESTERS AS ADDITION PRODUCTS.
  187643. 14464N
  187644. 2/28/96
  187645. AkNEW RING
  187646. OPENING REACTION OF THIIRANES WITH CARBOXYLIC ACID DERIVATIVES CATALYZED BY QUATERNARY ONIUM SALTS
  187647. 1994 X    4571
  187648. 4574Y
  187649. 13456
  187650. LANDAIS, Y.
  187651. Tet. Lett.
  187652. SILYL CARBONYL
  187653. COMPOUNDS ONE
  187654. POT SYNTHESIS ENANTIOSELECTIVE SYNTHESIS HYDROSILYLATION CATALYSTS DIAZO ESTERS KETONES COMPLEXES ALDEHYDES 
  187655.  DIAZO CHIRAL INSERTION SILYL SILICON CARBENOID RHODIUM ASYMMETRIC MECHANISM CH WRITING
  187656. /ALPHA
  187657. SILYL
  187658. ALPHA
  187659. SUBSTITUTED ACETIC ESTERS HAVE BEEN PREPARED IN GOOD YIELDS AND REASONABLE DIASTEREOSELECTIVITIES USING AN ASYMMETRIC METAL CARBENE INSERTION INTO THE SI
  187660. H BOND. OPTICALLY ACTIVE 1,2
  187661. DIOLSWERE THEN PREPARED AFTER REDUCTION OF THE ESTER AND CONVERSION OF THE C
  187662. SI BOND INTO A C
  187663. OH BOND.
  187664. 14465N
  187665. 2/28/96
  187666. A6ASYMMETRIC METAL CARBENE INSERTION INTO THE SI
  187667. H BOND.
  187668. 1994 X    4565
  187669. 4568Y
  187670. 13457
  187671. NOWOTNY, S.
  187672. Tet. Lett.
  187673. CoDISULFONAMIDE
  187674. DIALKYL ZINC SYSTEM FUNCTIONALIZED SECONDARY ALCOHOLS EXCHANGE
  187675. REACTION ALKYLATION 
  187676. UTHE USE OF TI(OT
  187677. BU)(4) OR RELATED BULKY TITANIUM(IV)ALKOXIDES, AS COCATALYSTS INSTEAD OF TI(OI
  187678. PR)(4) IN THE ENANTIOSELECTIVE ADDITION OF DIMETHYL ZINC TO ALDEHYDES INTHE PRESENCE OF THE CATALYST 2 (8 MOL%) LEADS TO A DRAMATIC IMPROVEMENT OF THE ENANTIOSELECTIVITY (0%EE TO93%EE). THE SCOPE AND THE LIMITATIONS OF THIS EFFECT ARE DESCRIBED.
  187679. 14466N
  187680. 2/28/96
  187681. AjDRAMATIC TITANIUM ALKOXIDE EFFECT IN THE CATALYTIC ENANTIOSELECTIVE ADDITION OF DIALKYLZINCS to ALDEHYDES.
  187682. 1994 X    4539
  187683. 4540Y
  187684. 13458
  187685. DENIS, R. C.
  187686. GRAVEL
  187687. Tet. Lett.
  187688. RING EXPANSION RATE CONSTANTS VINYL CYCLOPROPANES KINETICS 
  187689. VINYL RADICAL REARRANGEMENT THIOPHENYL CYCLIZATION INTRAMOLECULAR CYCLOPROPYL CARBINYL ELIMINATION ADDITION ALKENE
  187690. tA NEW METHODOLOGY ALLOWING TO ASSEMBLE FUSED VINYLCYCLOPROPANES BY CYCLIZATION OF VINYL RADICALS IS HEREIN REPORTED. THIS METHODOLOGY IS BASED ON THE TRAPPING OF THE CYCLOPROPYLCARBINYL RADICAL INTERMEDIATE BY BPHENYLTHIYL ELIMINATION WHICH PROVIDES THEVINYLCYCLOPROPANE. PRELIMINARY RESULTS ON A FEW MODELCOMPOUNDS ILLUSTRATE THE FEASIBILITY AND USEFULNESS OF THE METHOD.
  187691. 14467N
  187692. 2/28/96
  187693. A>NEW ACCESS to FUSED VINYLCYCLOPROPANES BY RADICAL CYCLIZATION.
  187694. 1994 X    4531
  187695. 4534Y
  187696. 13459
  187697. ANGLE, S. R.
  187698. Tet. Lett.C
  187699. CATIONS 
  187700. vINTRAMOLECULAR CYCLIZATION OF BENZYLIC CATIONS DERIVED FROM P
  187701. QUINONE METHIDES 5 AND 6, AFFORDED THE CORRESPONDING SIX
  187702.  OR SEVEN
  187703. MEMBERED RING PRODUCTS 7 OR 9 DEPENDING ON THE SUBSTITUTION OF THE ALKENE. DEUTERIUM LABELING EXPERIMENTS INDICATED THAT FORMATION OF 9 OCCURRED VIA A 1,3
  187704. HYDROGEN SHIFT, WHEREAS FORMATION OF 7 PROCEEDED VIA TWO SEQUENTIAL 1,2
  187705. HYDRIDE TRANSFERS.
  187706. 14468N
  187707. 2/28/96
  187708. AvMECHANISM OF P
  187709. QUINONE METHIDE INITIATED CYCLIZATION REACTIONS TERMINATED BY ALKENES:  1,2
  187710.  VS 1,3
  187711. HYDROGEN MIGRATION.
  187712. 1994X    4519
  187713. 4522Y
  187714. 13460
  187715. MCMURRY, J. E.
  187716. Tet. Lett.
  187717.     CZCOCKROACH SEX
  187718. PHEROMONE AMERICAN COCKROACH (+/
  187719. CRASSIN REARRANGEMENT CONVERSION ALCOHOLS
  187720. 5WE HAVE CARRIED OUT AN ENANTIOSELECTIVE SYNTHESIS OF (
  187721. PERIPLANONE C BY A ROUTE INVOLVING TITANIUM
  187722. INDUCED, INTRAMOLECULAR PINACOL COUPLING REACTION OF A 1,10 KETOALDEHYDE AS THE KEY STEP. THE COUPLING OCCURS WITH PREDICTABLE STEREOCHEMISTRY TO GIVE A MIXTURE OF TWO DIOL PRODUCTS IN GREATER THAN 60% YIELD.
  187723. 14469N
  187724. 2/28/96
  187725. A?PERIPLANONE TOTAL SYNTHESIS VIA INTRAMOLECULAR PINACOL COUPLING
  187726. 1994 X    4505
  187727. 4508Y
  187728. 13461
  187729. BILLUPS, W. E.
  187730. Tet. Lett.C_CYCLOPROPARENES ACENE BISCYCLOPROPARENE POLYACENE CHEMISTRY REARRANGEMENTS MOLECULES POLYACENE K
  187731. CYCLOPROPARENES REACT WITH SILVER ION IN CHLOROFORM TO YIELD DIMERS WHICH CAN BE AROMATIZED BYDICHLORODICYANO QUINONE IN BENZENE TO GIVE THECORRESPONDING ACENE.
  187732. 14470N
  187733. 2/28/96
  187734. A-DIMERIZATION OF CYCLOPROPARENES BY SILVER ION
  187735. 1994 X    4493
  187736. 4496Y
  187737. 13462
  187738. LAGU, B. R.
  187739. Tet. Lett.CPHIGH DIASTEREOFACIAL SELECTIVITIES CHELATION CONTROL CHIRAL METHYL CONDENSATION K
  187740. KINETIC ENOLATES OF A NUMBER OF ALPHA
  187741. DIBENZYL)AMINOMETHYL KETONES WERE ALLOWED TO REACT WITH A VARIETY OF ALDEHYDES. HIGH DIASTEREOSELECTIVITY WAS OBSERVED FOR SODIUM ENOLATES COMPARED TO THEIR LITHIUM COUNTERPARTS.M
  187742. 14471N
  187743. 2/28/96
  187744. AhSURPRISINGLY HIGH DIASTEREOSELECTION IN THE ALDOL REACTIONS OF SODIUM ENOLATES OF A
  187745. AMINO METHYL KETONES
  187746. 1994X    4485
  187747. 4488Y
  187748. 13463
  187749. KINGSTON, D. G. I.
  187750. Tet. Lett.C'HEMISYNTHESIS ANALOGS EFFICIENT AGENTS K
  187751. TAXOL (1) CAN BE PREPARED IN GOOD YIELD BY COUPLING THE OXAZOLINE CARBOXYLIC ACID 5 WITH 7
  187752. (TRIETHYLSILYL)BACCATINIII, FOLLOWED BY HYDROLYSIS. THE OXAZOLINES 7 AND 8 CANALSO BE PREPARED DIRECTLY FROM TAXOL.M
  187753. 14472N
  187754. 2/28/96
  187755. AASYNTHESIS OF TAXOL FROM BACCATIN IN VIA AN OXAZOLINE INTERMEDIATE
  187756. 1994 X    4483
  187757. 4484Y
  187758. 13464
  187759. DIVONA, M. L.
  187760. Tetrahedron
  187761. QTHE ZN/ACOH REDUCTION OF 1 LEADS ONLY TO THE CARBONYLREDUCTION, WHILE C
  187762. DECYANATION OCCURS IN THE CASE OF 2.THE MECHANISM OF THE FATTER REACTION IS DISCUSSED. THE N
  187763. DECYANATION OF N
  187764. CYANOAMINES 3 AND 4 INVOLVES AN IONICMECHANISM, LEADING TO N
  187765. ACYL DERIVATIVES AND ISOCYANICACID THE LATTER COMPOUND BEING ULTIMATELY REDUCED TOFORMIC ACID.
  187766. 14473N
  187767. 2/28/96
  187768. AqZINC
  187769. PROMOTED REACTIONS .9. THE FATE OF THE CYANO GROUP IN THE REDUCTION OF SIMPLE CYANOKETONES AND N
  187770. CYANOAMINES
  187771. 1994 X    8203
  187772. 8208Y
  187773. 13465
  187774. BATRA, M. S.
  187775. Tetrahedron
  187776. C^STEREOSELECTIVE SYNTHESIS ASYMMETRIC
  187777. SYNTHESIS REDUCTION KETONES 1,3
  187778. DIOLS INDUCTION REAGENTS 
  187779. THE INTRINSIC STEREOSELECTIVITY OF THE CYANIDE ADDITION TOBETA
  187780. HYDROXYKETONES IN THE PRESENCE OF 18
  187781. CROWN
  187782. 6 OR ZNI2IS LOWER THAN THAT PREVIOUSLY REPORTED. HOWEVER, THE REACTION BEARS A PRACTICAL VALUE IN THAT SYN BETA
  187783. HYDROXYCYANOHYDRINS AND ANTI 2,4
  187784. DIHYDROXYAMIDES CAN BE DIASTEREOSELECTIVELY OBTAINED IN REASONABLE YIELDS IN AONE
  187785. POT PROCEDURE. THE HIGH D.E.'S INITIALLY REPORTED WERE DUE TO THE WORK
  187786. UP PROCEDURE, WHERE THE HCL CONVERTED MUCHFASTER THE ANTI BETA
  187787. HYDROXYCYANOHYDRIN THAN THEB6 SYN PRODUCT INTO THE CORRESPONDING AMIDE. THIS FASTER
  187788. 14474N
  187789. 2/28/96
  187790. ON THE DIASTEREOSELECTIVITY OF CYANIDE ADDITION to b
  187791. HYDROXYKETONES:  ONE
  187792. POT SYNTHESIS of SYN-b
  187793. HYDROXY CYANOHYDRINS AND ANTi-2,4
  187794. DIHYDROXYAMIDES
  187795. 1994 X    8169
  187796. 8184Y
  187797. 13466
  187798. A    BASSA, J.
  187799. TetrahedronCSMECHANISTIC ASPECTS COPPER HYDRIDE 5
  187800. METHYLENE
  187801. 2(5H)
  187802. FURANONE REDUCTIONS COMPLEXES 
  187803. <SEVERAL TITLE COMPOUNDS CONTAINING ALDEHYDE, KETONE OR UNSATURATED ESTER FUNCTIONS IN SIDE
  187804. CHAINS AT C
  187805. 5 POSITIONHAVE BEEN SYNTHESIZED FOR THE FIRST TIME. THE ABILITY OFSOME OF THESE COMPOUNDS AS PRECURSORS IN THE PREPARATION OF POLYFUNCTIONAL CYCLOPENTADIENE OR SPIRO[4.4]NONANEDERIVATIVES HAS SHOWN TO BE FEASIBLE.
  187806. 14475N
  187807. 2/28/96
  187808. AvSYNTHESIS OF 5,5
  187809. DISUBSTITUTED 2(3H)
  187810. DIHYDRO FURANONES CONTAINING SIDE
  187811. CHAIN CARBONYL FUNCTIONS, AND SOME DERIVATIVES.
  187812. 1994X    8143
  187813. 8152Y
  187814. 13467
  187815. CHANDRASEKHAR, S.
  187816. TetrahedronC
  187817. ORTHO
  187818. ESTERS HYDROLYSIS 
  187819. ;THE NOVEL ALKYLLITHIUM 1B IS NOT ONLY INTRIGUINGLY STABLETOWARDS FRAGMENTATION, BUT ALSO A SYNTHETICALLY USEFUL REAGENT, COMPLEMENTING CURRENT CARBOXYLIC ESTER ENOLATE METHODOLOGY. ITS DESIGN IS BASED ON INTERESTING MECHANISTIC PRINCIPLES, AND HARNESSES THE KNOWN STABILITY OF THE 2,4,10
  187820. TRIOXAADAMANTANE FRAMEWORK.
  187821. 14476N
  187822. 2/28/96
  187823. AoA b,b,b
  187824. TRIALKOXYETHYLLITHIUM STABLE TOWARDS FRAGMENTATION:  A CARBOXYL PROTECTED ACETIC ACID DIANION QUIVALENT
  187825. 1994X    8099
  187826. 8102Y
  187827. 13468
  187828. PALE, P.
  187829. Tetrahedron
  187830. ALDER CYCLOADDITIONS OCCURRING TERPENE DERIVATIVES MODELING CHEMICAL
  187831. REACTIVITY MACROLIDE TOTAL SYNTHESIS DIELS
  187832. ALDER TRANSITION STRUCTURES ALLYLIC SUBSTITUENTS ORGANIC
  187833. REACTIONS ENOL ETHERS STEREOSELECTIVITY 
  187834. HETERO DIELS
  187835. ALDER REACTION OF OXADIENES WITH 3,4
  187836. EPOXY
  187837. METHYLENE OXOLANES GAVE THE CORRESPONDING 3,4
  187838. EPOXY
  187839. DIOXASPIRO[4,5]
  187840. ENES WITH HIGH STEREOSELECTIVITY GOOD YIELDS OF ADDUCTS WERE OBTAINED IN THE PRESENCE OF MILD LEWIS ACIS, SUCH AS ZINC OR STANNOUS CHLORIDE. THESPIROKETAL ADDUCTS HAVE BEEN TRANSFORMED CHEMIO
  187841.  ANDSTEREOSPECIFICALLY BY EITHER HYDROGENATION, HYDRIDE REDUCTION OR ACID CATALYZED ISOMERIZATION. THE STEREOCHEMICAL OUTCOME OF THE CYCLOADDITIONS HAS BEENI NVESTIGAB1TED. THE SPIROKETAL ADDUCTS ALWAYS RESULT FROM AN
  187842. 14477N
  187843. 2/28/96
  187844. FACIAL DIASTEREOSELECTION IN [4+2]
  187845. CYCLOADDITIONS OF 3,4
  187846. EPOXY
  187847. METHYLENEOXOLANES WITH OXADIENES:  A SHORT SYNTHESIS OF SPIROKETALS.
  187848. 1994 X    8035
  187849. 8052Y
  187850. 13469
  187851. HARADA, T.
  187852. TetrahedronC
  187853. CHIRAL ORGANOMETALLIC REAGENTS ALPHA
  187854. BROMOALKYLLITHIUM COMPOUNDS HALOGEN INTERCHANGE REACTION PURE VINYLLITHIUM REAGENT SINGLE
  187855. ELECTRON
  187856. TRANSFER CARBON BOND FORMATION STEREOSELECTIVE ADDITION ALKYL
  187857. HALIDES LITHIUM MECHANISM 
  187858. STEREOCHEMISTRY IN GENERATION OF LITHIUM AND ZINCATE CARBENOIDS BY BROMINE/ METAL EXCHANGE REACTIONS OF GEM
  187859. DIBROMO COMPOUNDS WITH BULI AND LITHIUM TRIORGANO ZINCATES,RESPECTIVELY, HAS BEEN INVESTIGATED. BOTH LITHIUM AND ZINCATE CARBENOIDS DERIVED FROM 1,1
  187860. DIBROMOALKENES ARE DEMONSTRATED TO BE CONFIGURATIONALLY STABLE AT LOW TEMPERATURES WHEREAS, IN THE PRESENCE OF THE UNREACTED STARLING DIBROMOALKENES, THE LITHIUM CARBENOIDS, BUT NOTTHE ZINCATE CARBENOIDS, UNDERGO FACILE ISOMERIZATION ATTB:HE CARBENOID CARBONS. ZINCATE CARBENOIDS DERIVED FROM 1,1
  187861. 14478N
  187862. 2/28/96
  187863. AxSTEREOCHEMISTRY IN CARBENOID FORMATION BY BROMINE / LITHIUM AND BROMINE/ ZINC EXCHANGE REACTIONS OF GEM
  187864. DIBROMOCOMPOUNDS
  187865. 1994 X    7987
  187866. 8002Y
  187867. 13470
  187868. KAMIMURA, A.
  187869. TetrahedronM
  187870. 14479N
  187871. 2/28/96
  187872. AsREVERSING THE REGIOCHEMICAL COURSE OF 1,3
  187873. DIPOLAR CYCLOADDITION OF NITRILE OXIDES BY MODIFICATION OF DIPOLAROPHILES
  187874. 1994 X    7969
  187875. 7980Y
  187876. 13471
  187877. MORIYA, T.
  187878. TetrahedronCfPROPARGYL CARBONATES NEUTRAL CONDITIONS CARBONUCLEOPHILES CARBONYLATION HYDROBORATION COMPLEXES ROUTE 
  187879. A SYNTHESIS OF 2
  187880. ALKENYL)
  187881. , AND 2
  187882. ALKYL
  187883. BUTADIENE DERIVATIVES (2) BY THE PALLADIUM
  187884. CATALYZED CROSS
  187885. COUPLING REACTION OF 2,3
  187886. BUTADIENYL CARBONATES (1) WITH 9
  187887. ALKYL
  187888. BICYCLO[3.3.1]NONANES (9
  187889. ALKYL
  187890. BBN), 1
  187891. ALKENYLBORONIC ACIDS, OR ARYLBORONIC ACIDS IS DESCRIBED. THE REACTION PROCEEDED REGIOSELECTIVELY WITH THE PALLADIUM
  187892. PHOSPHINE COMPLEXES UNDER NEUTRAL CONDITIONS.
  187893. 14480N
  187894. 2/28/96
  187895. A NEW FACILE SYNTHESIS OF 2
  187896. SUBSTITUTED 1,3
  187897. BUTADIENE DERIVATIVES VIA PALLADIUM
  187898. CATALYZED CROSS
  187899. COUPLING REACTION OF 2,3
  187900. ALKADIENYL CARBONATES WITH ORGANOBORON COMPOUNDS
  187901. 1994X    7961
  187902. 7968Y
  187903. 13472
  187904. A    DUBAU, N.
  187905. OrganometallicsC(RAY CRYSTAL
  187906. STRUCTURE REACTIVITY IMINES M
  187907. 14481N
  187908. 2/28/96
  187909. EFFECTS OF A STRONG ELECTRON
  187910. WITHDRAWING N
  187911. BORTYLSUBSTITUENT ON THE STABILITY OF NITRILIMINES 
  187912.  SURPRISING DIMERIZATION INVOLVING THE NITRILIMINE HETEROATOMSUBSTITUENTS WITH FORMATION OF (FUSED) BICYCLIC [3.3.0] AND [4.3.0] DERIVATIVES
  187913. 1994 X    2913
  187914. 2916Y
  187915. 13473
  187916. FEIKEN, N.
  187917. OrganometallicsC
  187918. M FRAGMENT DIMETHYL ACETYLENEDICARBOXYLATE (1,4
  187919. DIAZA
  187920. DIENE)TRICARBONYLIRON 1,5
  187921. DIHYDROPYRROL
  187922. ONES COMPLEXES ALKYNE INTERMEDIATE (DAD)FE(CO)3 LIGAND M
  187923. 14482N
  187924. 2/28/96
  187925. DIPOLAR CYCLOADDITION to THE FE
  187926. N=C FRAGMENT .14. AROMATIC ISOTHIOCYANATES AS DIPOLAROPHILES 
  187927.  REVERSIBLE FORMATION OF NOVEL [3.2.2] BICYCLIC DOUBLE ISOCYANIDE INSERTION PRODUCTS 
  187928.  THERMODYNAMICS OF ISOCYANIDE INSERTION REACTION
  187929. 1994 X    2825
  187930. 2832Y
  187931. 13474
  187932. FLATT, B. T.
  187933. OrganometallicsCVOLEFIN METATHESIS VINYLCARBENE COMPLEXES ALKYLIDENE COMPLEXES CYCLOPROPENES CATALYSTS M
  187934. 14483N
  187935. 2/28/96
  187936. AMSYNTHESIS, STRUCTURE, AND REACTIVITY OF A RHENIUM OXO
  187937. VINYLALKYLIDENE COMPLEX
  187938. 1994 X    2728
  187939. 2732Y
  187940. 13475
  187941. WISSING, E.
  187942. OrganometallicsC5X
  187943. RAY STRUCTURE CARBON BOND FORMATION COMPLEXES ZINC M
  187944. 14484N
  187945. 2/28/96
  187946. AMORGANOZINC A
  187947. DIIMINE RADICALS 
  187948.  SYNTHESIS AND REACTIVITY TOWARD ALKYL HALIDES
  187949. 1994X    2602
  187950. 2608Y
  187951. 13476
  187952. KNIGHT, K. S.
  187953. Organometallics
  187954. ALLYLIC ZIRCONIUM REAGENTS BOND
  187955. FORMING REACTION THIOALDEHYDE COMPLEXES MAGNESIUM REAGENTS GRIGNARD
  187956. REAGENTS ETHER DERIVATIVES RING CONTRACTION METAL CATALYSIS ALKYL
  187957. ALKENE ETHYLMAGNESATION M
  187958. 14485N
  187959. 2/28/96
  187960. AVSTEREOSELECTIVE CYCLIZATION VIA ZIRCONOCENE
  187961. CATALYZED INTRAMOLECULAR OLEFIN ALLYLATION
  187962. 1994 X    2575
  187963. 2577Y
  187964. 13477
  187965. HOJO, M.
  187966. J. Organomet. Chem.CGSILANE VINYLOXIRANE ACETAL ALLYLATION ALLYLSILANE REAGENTS SIGMA HOJO MM
  187967. 14486N
  187968. 2/28/96
  187969. STUDIES ON ORGANOSILICON CHEMISTRY .122. REACTION OF 2
  187970. OXIRANYLALLYLSILANES WITH ACETALS 
  187971.  DIRECT INTRODUCTION OF A VINYLOXIRANE MOIETY
  187972. 1994 X
  187973. PP C1
  187974. 13478
  187975. MANDAI, T.
  187976. J. Organomet. Chem.C
  187977. PALLADIUM CATALYSIS 2
  187978. ALKYNYL CARBONATE 2
  187979. ALKYNYL FORMATE CONJUGATED ENYNE DISUBSTITUTED ALKYNE SYNTHETIC METHOD ALLYLIC CARBONATES AMMONIUM FORMATE PROPARGYLIC CARBONATES M
  187980. 14487N
  187981. 2/28/96
  187982. PALLADIUM
  187983. CATALYZED HYDROGENOLYSIS OF 2
  187984. ALKYNYL FORMATES AND ELIMINATION OF 2
  187985. ALKYNYL CARBONATES 
  187986. ALKYNYLPALLADIUM COMPLEX VS ALLENYL PALLADIUM COMPLEX AS INTERMEDIATES
  187987. 1994X
  187988. PP 343
  187989. 13479
  187990. SUZUKI, N.
  187991. J. Organomet. Chem.C
  187992. ZIRCONIUM SILICON METALLOCENES CARBON CARBON BOND FORMATION ALDEHYDE KETONE METAL
  187993. PROMOTED CYCLIZATION GRIGNARD
  187994. REAGENTS CONVENIENT METHOD ETHYLENE COMPLEX M
  187995. 14488N
  187996. 2/28/96
  187997. AXHIGHLY REGIOSELECTIVE REACTION OF ZIRCONOCENE
  187998. ALKENE COMPLEXES WITH ALDEHYDES OR KETONES
  187999. 1994 X
  188000. PP 117
  188001. 13480
  188002. MURAKAMI, M.
  188003. J. Organomet. Chem.C
  188004. SAMARIUM CARBON CARBON BOND FORMATION ORGANIC
  188005. SYNTHESIS RADICAL TRANSLOCATION CRYSTAL
  188006. STRUCTURE ALPHA HALIDES CYCLIZATION IODIDE ISOCYANIDES M
  188007. 14489N
  188008. 2/28/96
  188009. AOCARBON
  188010. CARBON BOND FORMING REACTIONS VIA NEW ORGANO SAMARIUM(III) INTERMEDIATES
  188011. 1994X
  188012. PP 93
  188013. 13481
  188014. A    KANDA, T.
  188015. J. Organomet. Chem.CkTELLURIUM LITHIUM ALLYL BENZYL HALIDE ORGANOTELLURIUM CHEMISTRY ALDEHYDES REARRANGEMENT REACTIVITY REAGENT M
  188016. 14490N
  188017. 2/28/96
  188018. GENERATION OF ALLYL LITHIUMS AND BENZYL LITHIUMS FROM THE CORRESPONDING HALIDES BY THE AID OF LITHIUM
  188019. TELLURIUM EXCHANGE REACTIONS
  188020. 1994X
  188021. PP 71
  188022. 13482
  188023. FUJIWARA, J
  188024. J. Organomet. Chem.
  188025. ALLYLTIN VINYL CARBENE MONOTERPENE LEWIS ACID BIFUNCTIONAL REAGENT ORGANIC SYNTHESIS REGIOSPECIFIC SYNTHESIS CYCLOPROPYL KETONES TRIALKYLSTANNYLMETHYLLITHIUM REARRANGEMENT M
  188026. 14491N
  188027. 2/28/96
  188028. DIVERSITY IN THE REACTION MODES OF ANIONIC AND CATIONIC STANNYL REAGENTS 
  188029. CHLORO ALLYLSTANNANES AS A VINYL CARBENE EQUIVALENT, AND ITS APPLICATION FOR (+/
  188030. BAKUCHIOL SYNTHESIS
  188031. 1994 X
  188032. PP 63
  188033. 13483
  188034. Ma, J.B
  188035. Heterocycles
  188036.  CeFUNCTIONALIZED CIS
  188037. HYDROISOQUINOLINES MANZAMINE
  188038. A TRICYCLIC HEART ALKALOIDS CORE SUBSTRUCTURE SPONGE M
  188039. 14492N
  188040. 2/28/96
  188041. AhHYDROISOQUINOLINE RING CONSTRUCTION VIA THE DIELS
  188042. ALDER REACTION OF ARE COLONE
  188043. DERIVED ENOL SILYL ETHERS
  188044. 1994 X    1609
  188045. 1618Y
  188046. 13484
  188047. BROGGINI, G.
  188048. HeterocyclesM
  188049. 14493N
  188050. 2/28/96
  188051. INTRAMOLECULAR NITRILE IMINE CYCLOADDITIONS to THE ACETYLENIC BOND IN THE SYNTHESIS OF PYRAZOLO[1,5
  188052. A][4,1]
  188053. BENZOXAZEPINES AND PYRAZOLO[1,5
  188054. A][5,1]BENZOXAZOCINES
  188055. 1994X    1601
  188056. 1607Y
  188057. 13485
  188058. KOYAMA, J.
  188059. HeterocyclesM
  188060. 14494N
  188061. 2/28/96
  188062. A<DIELS
  188063. ALDER REACTION OF 1,2,3
  188064. TRIAZINE WITH ALDEHYDE ENAMINE
  188065. 1994 X    1595
  188066. 1600Y
  188067. 13486
  188068. A    BLOCH, R.
  188069. HeterocyclesCCCOMMON CHIRAL SYNTHON ENANTIOMERS ALKALOIDS INDOLIZIDINES LACTONES M
  188070. 14495N
  188071. 2/28/96
  188072. A6AN ENANTIOSELECTIVE SYNTHESIS OF (+)
  188073. INDOLIZIDINE
  188074. 1994X    1589
  188075. 1594Y
  188076. 13487
  188077. MOLDVAI, I.
  188078. HeterocyclesM
  188079. 14496N
  188080. 2/28/96
  188081. AhSYNTHESIS OF VINCA ALKALOIDS AND RELATED COMPOUNDS .69. SYNTHESIS OF 15
  188082. SUBSTITUTED EBURNANE DERIVATIVES
  188083. 1994 X    1541
  188084. 1550Y
  188085. 13488
  188086. %A    Wu, H. J.C
  188087. TRANSFER
  188088. REACTION OCCURRING FUSED FURANS CYCLOADDITION BASIC SKELETON ESTER DIENOPHILES KEY INTERMEDIATE ALLENECARBOXYLATE CONSTRUCTION M
  188089. 14497N
  188090. 2/28/96
  188091. INTRAMOLECULAR DIELS
  188092. ALDER REACTION OF FURANS WITH ALLENYLETHERS 
  188093.  HIGH EFFECT OF THE CHAIN LENGTH ON THE STRUCTURE AND REACTIVITY OF THE CYCLOADDUCTS
  188094. 13489
  188095. TOYOTA, M.
  188096. HeterocyclesC"DIELS
  188097. ALDER REACTIONS RING
  188098. SYSTEM M
  188099. 14498N
  188100. 2/28/96
  188101. LEWIS ACID PROMOTED TANDEM [4+2] CYCLOADDITION
  188102. REARRANGEMENT PROCESS 
  188103.  A SIMPLE AND EFFICIENT SYNTHESIS OF HIGHLY FUNCTIONALIZED OXABICYCLO[3.3.1]NONANES
  188104. 1994X    1491
  188105. 1496Y
  188106. 13490
  188107. TSUKAYAMA, M.
  188108. HeterocyclesC
  188109. ISOFLAVONE M
  188110. 14499N
  188111. 2/28/96
  188112. AeREGIOSELECTIVE PRENYLATION OF PHENOLS BY PALLADIUM CATALYST 
  188113.  SYNTHESES OF PRENYLPHENOLS AND CHROMANS
  188114. 1994X    1487
  188115. 1490Y
  188116. 13491
  188117. GALAMBOS, G.
  188118. HeterocyclesC0RADICAL CHAIN REACTIONS ORGANIC
  188119. SYNTHESIS DESIGNM
  188120. 14500N
  188121. 2/28/96
  188122. A3ADDITION OF THIOLS to ACETYLENE SUBSTITUTED INDOLES
  188123. 1994 X    1459
  188124. 1464Y
  188125. 13492
  188126. FUXREITER, M.
  188127. HeterocyclesM
  188128. 14501N
  188129. 2/28/96
  188130. FORMATION OF A STRAINED TRIAZAPENTALENOINDENE SKELETON VIA THE REARRANGEMENT OF 2,3
  188131. DIHYDRO
  188132. NITRO
  188133. IMIDAZO[2,1
  188134. PHTHALAZIN
  188135. OLATE EFFECTED BY DICHLOROACETIC ANHYDRIDE
  188136. 1994 X    1453
  188137. 1457Y
  188138. 13493
  188139. BILLUPS, W. E.
  188140. JACSC}SPIROCONJUGATION CYCLOPROPENE CYCLOPENTADIENE SPIROTRIENE DESILYLATION ELIMINATION FLUORIDE SILICON DEHYDROBROMINATION STRAINM
  188141. 14502N
  188142. 2/28/96V
  188143. SPIRO[2.4]HEPTA
  188144. 1,4,6
  188145. TRIENEW
  188146. 1994 X
  188147. 6463Y
  188148. 13494
  188149. NISHIDA, M.
  188150. JACSM
  188151. 14503N
  188152. 2/28/96
  188153. A^LEWIS ACID
  188154. PROMOTED DIASTEREOSELECTIVE RADICAL CYCLIZATION USING CHIRAL A,b
  188155. UNSATURATED ESTERS
  188156. 1994X    6455
  188157. 6456Y
  188158. 13495
  188159. HSUNG, R. P.
  188160. JACSM
  188161. 14504N
  188162. 2/28/96
  188163. AgFIRST STEREOSELECTIVE SYNTHESIS OF ARENE CHROMIUM TRICARBONYL COMPLEXES VIA THE BENZANNULATION REACTION
  188164. 1994X    6449
  188165. 6450Y
  188166. 13496
  188167. POST, A. J.
  188168. JACSM
  188169. 14505N
  188170. 2/28/96
  188171. AoPHOTOLYTIC REARRANGEMENT OF 2
  188172. ISOBUTYL
  188173. OXAZASPIRO[2.5]OCTANE. SENSITIZED PHOTOISOMERIZATION OF OXAZIRIDINES
  188174. 1994X    6439
  188175. 6440Y
  188176. 13497
  188177. SHIMANO, N.
  188178. JACSM
  188179. 14506N
  188180. 2/28/96
  188181. AfASYMMETRIC MICHAEL
  188182. TYPE ADDITIONS OF LITHIUM AMIDES to AROMATIC SYSTEMS LEADING to NOVEL b
  188183. AMINO ACIDS
  188184. 1994X    6437
  188185. 6438Y
  188186. 13498
  188187. BARTA, N. S.
  188188. JACSCsMICHAEL
  188189. TYPE ALKYLATION ENANTIOSELECTIVE SYNTHESIS CARBON CENTERS KETO
  188190. ESTERS TRANSITION
  188191. STATE IMINES CONSTRUCTION M
  188192. 14507N
  188193. 2/28/96
  188194. AvASYMMETRIC FORMATION OF QUATERNARY CENTERS THROUGH AZA
  188195. ANNULATION OF CHIRAL b
  188196. ENAMINO ESTERS WITH ACRYLATE DERIVATIVES
  188197. 1994 X    6201
  188198. 6206Y
  188199. 13499
  188200. NORO, M.
  188201. IWAMURA B
  188202. SOLID
  188203. STATE POLYMERIZATION ELECTRON
  188204. RESONANCE SINGLET
  188205. TRIPLET GAPS ORGANIC FERROMAGNETS GROUND
  188206. STATE SUBSTITUTED CARBENES WOLFF REARRANGEMENT PHENYL RING MOLECULES SPECTROSCOPY 
  188207. CARBENE ALKYNE REARRANGEMENT SPECTROSCOPY WRITING DIAZO EPR INTERCONVERSION
  188208. 14508N
  188209. 2/28/96
  188210. AHCARBENE
  188211. CARBENE INTERCONVERSION BETWEEN 1
  188212.  AND 3
  188213. PHENYL
  188214. PROPYNYLIDENES
  188215. 1994X    6179
  188216. 6190Y
  188217. 13500
  188218. LIKHOTVORIK, I. R.
  188219. JONESB
  188220. JACSC
  188221. OPTICALLY
  188222. ACTIVE CYCLOPROPENE C3H4 SURFACE GAS
  188223. PHASE ISOMERIZATION PYROLYSIS KINETICS BOND RACEMIZATION GENERATION ABINITIO 
  188224. CYCLOPROPENE THERMOLYSIS DIRADICAL CARBENE REARRANGEMENT NOVEL MECHANISM VINYLIDENE WRITINGM
  188225. 14509N
  188226. 2/28/96
  188227. APVINYLIDENES AS INTERMEDIATES IN THERMAL CYCLOPROPENE
  188228. ACETYLENE REARRANGEMENTS
  188229. 1994X    6175
  188230. 6178Y
  188231. 13501
  188232. DELLA, E. W.
  188233. JACSC
  188234. NUCLEOPHILIC SOLVENT ASSISTANCE INDUCTIVE CHARGE DISPERSAL SN2 INTERMEDIATE MECHANISM REACTION
  188235. RATES SN2
  188236. SN1 SPECTRUM CUBYL CATION FORCE
  188237. FIELD CARBENIUM IONS CONSTANTS 1,3
  188238. DIIODOBICYCLO<1.1.1>PENTANE M
  188239. 14510N
  188240. 2/28/96
  188241. AxBRIDGEHEAD CARBOCATIONS:  A SOLVOLYTIC STUDY OF 1
  188242. BROMOBICYCLO[1.1.1.]PENTANE AND ITS BRIDGEHEAD
  188243. SUBSTITUTED DERIVATIVES
  188244. 1994  X    6159
  188245. 6166Y
  188246. 13502
  188247. MARUOKA, K.
  188248. LIVER ESTERASE DEHYDROGENASE
  188249. CATALYZED OXIDATIONS LEWIS ACID COMPLEXES ORGANIC
  188250. SYNTHESIS BUILDING
  188251. BLOCKS MESO
  188252. DIESTERS ENANTIOSELECTIVE HYDROLYSIS C
  188253. NUCLEOSIDES ENZYMES DERIVATIVES M
  188254. 14511N
  188255. 2/28/96
  188256. ASYMMETRIC DIELS
  188257. ALDER REACTION OF UNSYMMETRICAL MALEATES. A CHEMICAL ACCESS to CHIRAL, UNSYMMETRICAL CIS
  188258. CYCLOHEXENE
  188259. DICARBOXYLATES
  188260. 1994 X    6153
  188261. 6158Y
  188262. 13503
  188263. YANAGISAWA, A.
  188264. JACSC
  188265. ALLYLIC ORGANOCOPPER REAGENTS F3
  188266. ALPHA METHYL
  188267. ESTER CONJUGATE ADDITION REGIOREVERSED ADDITION RADICAL
  188268. ANIONS ALPHA,BETA
  188269. UNSATURATED KETONES BETA,GAMMA
  188270. UNSATURATED ACIDS STEREOSPECIFIC SYNTHESIS CATALYZED CARBONYLATION ALLYLCARBOXYLIC ACIDS M
  188271. 14512N
  188272. 2/28/96
  188273. AjALLYLBARIUM REAGENTS:  UNPRECEDENTED REGIO
  188274.  AND STEREOSELECTIVE ALLYLATION REACTIONS OF CARBONYL COMPOUNDS
  188275. 1994X    6130
  188276. 6141Y
  188277. 13504
  188278. HARRIS, N. J.
  188279. ACCELERATED VINYLCYCLOPROPANE REARRANGEMENT ALIPHATIC CLAISEN REARRANGEMENT DEUTERIUM FRACTIONATION FACTORS TRANSITION
  188280. STATE STRUCTURE OXY
  188281. COPE REARRANGEMENT DIELS
  188282. ALDER REACTIONS ALKALI
  188283. METAL SALTS SUBSTITUTED CYCLOOCTENONES CYCLOPENTENE DERIVATIVES 3,3
  188284. SIGMATROPIC SHIFTS 
  188285. 14513N
  188286. 2/28/96
  188287. AGMECHANISM OF THE 1,3
  188288. SIGMATROPIC SHIFT OF 2
  188289. VINYLCYCLOBUTANOL ALKOXIDES
  188290. 1994  X    6121
  188291. 6129Y
  188292. 13505
  188293. Hwu, J. R.B
  188294. Helv. Chim. ActaC
  188295. ANTIBIOTICSM
  188296. 14514N
  188297. 2/28/96
  188298. A\SYNTHESES OF THE FIRST SELENIUM
  188299. CONTAINING BICYCLIC b
  188300. LACTAMS AS POTENT ANTIMICROBIAL AGENTS
  188301. 1994X    1037
  188302. 1045Y
  188303. 13506
  188304. A    PETIT, M.
  188305. Helv. Chim. ActaC
  188306. THIOCARBONYL YLIDES M
  188307. 14515N
  188308. 2/28/96
  188309. AsREACTION OF PHENYL DIAZOMETHANE WITH 1,3
  188310. THIAZOLE
  188311. 5(4H)
  188312. THIONES:  BASE
  188313. CATALYZED RING OPENING OF THE PRIMARY ADDUCT
  188314. 1994X    1076
  188315. 1086Y
  188316. 13507
  188317. NISHIO, T.
  188318. Helv. Chim. ActaC
  188319. NITROGEN
  188320. THIOCARBONYL SYSTEMS PHOTOCHEMICAL
  188321. REACTIONS THIOENAMIDE PHOTOCHEMISTRY PHOTOINDUCED REACTIONS THIOIMIDE SYSTEMS THIONE SYSTEMS PHOTOREACTIONS INDOLINE
  188322. THIONES PHOTOADDITION OLEFINS M
  188323. 14516N
  188324. 2/28/96
  188325. A8PHOTOCYCLOADDITION OF BENZOTHIAZOLE
  188326. THIONES to ALKENES
  188327. 1994X
  188328. 13508
  188329. ER, E.
  188330. Helv. Chim. ActaC
  188331. SILYL ENOL ETHERS M
  188332. 14517N
  188333. 2/28/96
  188334. AIPHOTOCHEMISTRY OF 6,6
  188335. DIMETHYL
  188336.  AND 2,2,6,6
  188337. TETRAMETHYL
  188338. 2H,6N
  188339. PYRAN
  188340. 1994X
  188341. 13509
  188342. NIESTROJ, M.
  188343. ELECTROPHILIC VINYLIC SUBSTITUTION ISOCYANATES ALPHA,BETA
  188344. UNSATURATED AMIDES, SYNTHESIS OF CARBODESTANNYLATION ALKENYLSTANNANES, APPLICATIONS OF M
  188345. 14518N
  188346. 2/28/96
  188347. TIN FOR ORGANIC SYNTHESIS .11. A MILD AND EFFECTIVE SYNTHESIS OF A,b
  188348. UNSATURATED CARBOXAMIDES AND SULFONAMIDES BY ELECTROPHILIC SUBSTITUTION OF ALKENYLSTANNANES WITH ISOCYANATES
  188349. 13510
  188350. ADAM, W.
  188351. Chem. Ber.C
  188352. EPOXIDATION DIOXIRANE, DIMETHYL BENZOFURANS, 2,3
  188353. DIMETHYL BENZOFURAN EPOXIDES QUINONE METHIDES [2+2] PHOTOCYCLOADDITION BENZOXETES HETERO
  188354. DIELS
  188355. ALDER REACTION ISOMERIZATION BENZOTHIETE M
  188356. 14519N
  188357. 2/28/96
  188358. PREPARATION OF 2H
  188359. BENZOXETES BY PHOTOINDUCED [2+2] CYCLOADDITION OF QUINONE METHIDES, ACCESSIBLE BY DIMETHYLDIOXIRANE (DMD) OXIDATION OF 2,3
  188360. DIMETHYLBENZOFURANS
  188361. 1994 X    1115
  188362. 1118Y
  188363. 13511
  188364. METZGER, J. O.
  188365. Chem. Ber.
  188366. RADICAL ADDITIONS ALKYL RADICALS STEREOSELECTIVITY HYDROGEN TRANSFER ISOSELECTIVE RELATIONSHIP CYCLOHEXANE ALKANES ALKENES ENOLATE MODEL M
  188367. 14520N
  188368. 2/28/96
  188369. ALSTEREOSELECTIVITY OF THE TRANSFER OF HYDROGEN ATOMS to CYCLIC ALKYL RADICALS
  188370. 1994X    1069
  188371. 1073Y
  188372. 13512
  188373. PRIMKE, H.
  188374. Chem. Ber.C
  188375. CYCLOPROPYL BUILDING BLOCKS STRAINED COMPOUNDS [4 + 2] CYCLOADDITION REGIOSELECTIVITY EPOXIDES, REGIOSELECTIVE CLEAVAGE OF OPTICALLY
  188376. ACTIVE OXAZOLIDINONES PERCHLORATE DIETHYL
  188377. ETHER BETA
  188378. AMINO ACIDS HIGH
  188379. PRESSURE FACILE CONSTRUCTIONM
  188380. 14521N
  188381. 2/28/96
  188382. NEW CYCLOPROPYL BUILDING BLOCKS FOR ORGANIC SYNTHESIS .21. DIELS
  188383. ALDER REACTIONS OF METHYL 2
  188384. CHLORO
  188385. CYCLOPROPYLIDENE ACETATE WITH ELECTRON
  188386. RICH DIENES 
  188387.  SYNTHESIS OF POTENTIAL INTERMEDIATES FOR ILLUDIN
  188388. 1994 X    1051
  188389. 1064Y
  188390. 13513
  188391. BECKHAUS, R.
  188392. Chem. Ber.C
  188393. METALLOCENE COMPLEXES, BENT TITANIUM COMPLEXES VINYLIDENE COMPLEXES TRANSITION METAL COMPLEXES HETERODINUCLEAR COMPLEXES CARBENE COMPLEXES EARLY
  188394. LATE HETERO DINUCLEAR COMPLEXES METALLACYCLES OXATITANA CYCLOBUTANE COMPLEXES OXATITANACYCLOPENTENE COMPLEXES M
  188395. 14522N
  188396. 2/28/96
  188397. CYCLIC ISOMERIC 4
  188398. MEMBERED AND 5
  188399. MEMBERED HETERO DINUCLEAR CARBENE COMPLEXES 
  188400.  FORMED FROM A TITANOCENE VINYLIDENE FRAGMENT AND METAL CARBONYLS
  188401. 1994 X    1003
  188402. 1013Y
  188403. 13514
  188404. GENNARI, C.
  188405. Tet. Lett.C
  188406. ACTIVE CHROMIUM(0)
  188407. COMPLEXED BENZALDEHYDE STEREOSELECTIVE SYNTHESIS ASYMMETRIC
  188408. SYNTHESIS ENANTIOSELECTIVE SYNTHESIS ORGANIC
  188409. SYNTHESIS ANTIBIOTIC X
  188410. 206 A
  188411. RING ANTI CONDENSATION TAXOL K
  188412. BORON ENOLATES DERIVED FROM ALPHA
  188413. HETEROSUBSTITUTED THIOACETATES AND BEARING MENTHONE
  188414. DERIVED CHIRAL LIGANDSREACT WITH ALDEHYDES TO GIVE ANTI ALDOLS WITH EXCELLENT DIASTERO
  188415.  AND ENANTIOCONTROL.M
  188416. 14523N
  188417. 2/28/96
  188418. A\A HIGHLY ENANTIO
  188419.  AND DIASTEREOSELECTIVE ALDOL REACTION FOR A
  188420. HETEROSUBSTITUTED THIOACETATES
  188421. 1994 X    4857
  188422. 4860Y
  188423. 13515
  188424. REUTRAKUL, V.
  188425. Tet. Lett.C
  188426. DERIVATIVES K
  188427. FLUORINE
  188428. FACILITATED CLAISEN REARRANGEMENT HAS BEEN EMPLOYED AS A KEY STEP IN THE SYNTHESIS OF ALPHA
  188429. FLUOROKETONES 5. THE ELIMINATION OF SULFENIC ACID FROM THEALLYL ETHERS 3 ARE EFFECTED UNDER FVP CONDITIONS.M
  188430. 14524N
  188431. 2/28/96
  188432. AMA NOVEL METHOD FOR THE SYNTHESIS OF A
  188433. FLUOROKETONES VIA CLAISEN REARRANGEMENT
  188434. 1994 X    4853
  188435. 4856Y
  188436. 13516
  188437. REUTRAKUL, V.
  188438. Tet. Lett.CvFLUOROORGANIC COMPOUNDS SELECTIVE FLUORINATION ELEMENTAL FLUORINE ORGANIC
  188439. SYNTHESIS SULFOXIDES REAGENTS DESIGN AGENTS K
  188440. FLUOROMETHYLKETONES 3 ARE SYNTHESIZED IN GOOD YIELDS BY AFLASH VACUUM PYROLYTIC ELIMINATION OF 2. STUDIES ON THE IMPROVED SYNTHESIS OF 2 LEADS TO THE EVIDENCE ON THE EXISTENCE OF ALPHA,ALPHA
  188441. DILITHIO FLUOROMETHYL PHENYLSULFOXIDE.M
  188442. 14525N
  188443. 2/28/96
  188444. AcAN IMPROVED PROCEDURE FOR THE SYNTHESIS OF FLUOROMETHYLKETONES:  FLASH VACUUM PYROLYTIC ELIMINATION
  188445. 1994X    4851
  188446. 4852Y
  188447. 13517
  188448. ARSENIYADIS, S.
  188449. Tet. Lett.C!PENTACYCLIC TRITERPENES ARBORANE 
  188450. THE AB+D 
  188451. > ABCD APPROACH FOR THE SYNTHESIS OF THE TETRACYCLIC INTERMEDIATES 3
  188452. 6 IS REINVESTIGATED. WATER,HIGH
  188453. PRESSURE, LICL AND SCANDIUM TRIFLATE
  188454. MEDIATED DIELS
  188455. ALDER REACTIONS OF 1 AND 2 ARE REPORTED.M
  188456. 14526N
  188457. 2/28/96
  188458. A=REGIO
  188459.  AND STEREOCHEMICAL VARIATIONS IN DIELS
  188460. ALDER REACTIONS
  188461. 1994 X    4843
  188462. 4846Y
  188463. 13518
  188464. GIUFFRIDA, D.
  188465. Tet. Lett.C:DIELS
  188466. ALDER OLIGOMERIZATIONS SUBSTRATE
  188467. DIRECTED SYNTHESIS 
  188468. DIMETHYLBENZO[1,2
  188469. C: 3,4
  188470. C']DIFURAN (7) IS A HIGHLY REACTIVE BISDIENE, WHICH UNDERGOES DIELS
  188471. ALDER REACTIONS WITH A WIDE VARIETY OF DIENOPHILES, INCLUDING DIMETHYL ACETYLENEDICARBOXYLATE AND CIS
  188472. DICHLOROBUT
  188473. ENE, TOGIVE PHENANTHRENE DERIVATIVES, E.G. 10 AND 12,RESPECTIVELY, FOLLOWING (HYDROGENATION AND) DEHYDRATION OFTHE BISADDUCTS 8 AND 11, RESPECTIVELY. 9,10
  188474. DIMETHYL
  188475. 1,4: 5,8
  188476. DIEPOXY
  188477. 1,4,5,8
  188478. TETRAHYDRO
  188479. PHENANTHRENE (5),  AS ARESULT OF THERMAL DECOMPOSITION OF EITHER (I) ITS BISAB6DDUCT 6 WITH TETRAPHENYLCYCLOPENTA
  188480. DIENONE OR (II) ITS
  188481. 14527N
  188482. 2/28/96
  188483. A'A NEW ROUTE to PHENANTHRENE DERIVATIVES
  188484. 1994 X    4839
  188485. 4842Y
  188486. 13519
  188487. HSIA, K. Y.
  188488. Tet. Lett.C
  188489. CYCLIZATION CARBOCYCLES ROUTES 
  188490. ALPHA
  188491. IODOS
  188492. DELTA
  188493.  AND 
  188494. GAMMA
  188495. HEXONOLACTONES WITH ALPHA,BETA
  188496. UNSATURATED ESTERS DEVELOPED FROM C
  188497. 6 UNDERGOBOTH TRIBUTYLTIN HYDRIDE
  188498. INDUCED RADICAL AND BASE CATALYSED ANIONIC MICHAEL CYCLISATIONS TO FORM BICYCLICLACTONES WITH VERY HIGHLY SUBSTITUTED HOMOCHIRALCYCLOPENTANES. THE DELTA
  188499. LACTONES GIVE CYCLOPENTANE PRODUCTS IN WHICH ADJACENT CARBON SUBSTITUENTS ON THE CYCLOPENTANE RING ARE CIS TO EACH OTHER, WHEREAS GAMMA
  188500. LACTONES GIVE CYCLOPENTANES IN WHICH THE CARBON CHAINS ARETRANS.
  188501. 14528N
  188502. 2/28/96
  188503. AxFORMATION OF HIGHLY SUBSTITUTED CYCLOPENTANES FROM RADICAL AND ANIONIC MICHAEL CYCLISATIONS OF A
  188504.  AND 
  188505. LACTONES
  188506. 1994 X    4823
  188507. 4826Y
  188508. 13520
  188509. HAYASHI, T.
  188510. Tet. Lett.C
  188511. OPTICALLY
  188512. ACTIVE ALLYLSILANES TRANSITION
  188513. METAL COMPLEXES ANTI STEREOCHEMISTRY ELECTROPHILIC SUBSTITUTION HYDROSILYLATION ALDEHYDES ALCOHOLS 
  188514. ALLYL SILANE REDUCTION PALLADIUM CARBONATE MECHANISM
  188515. TREDUCTION OF 3
  188516. ALKYL
  188517. TRIALKYLSILYL
  188518. PROPENYL METHYLCARBONATES WITH FORMIC ACID AND 1,8
  188519. BIS(DIMETHYLAMINO)NAPHTHALENE IN THE PRESENCE OF APALLADIUM CATALYST (3 MOL %) COORDINATED WITH (R)
  188520. DIPHENYLPHOSPHINO
  188521. METHOXY
  188522. BIPHENANTHRYL (MOP
  188523. PHEN) GAVE OPTICALLY ACTIVE ALLYLSILANES (3
  188524. ALKYL
  188525. TRIALKYLSILYL
  188526. PROPENES) OF UP TO 91% EE.
  188527. 14529N
  188528. 2/28/96
  188529. AwASYMMETRIC SYNTHESIS OF ALLYLSILANES BY PALLADIUM
  188530. CATALYZED ASYMMETRIC REDUCTION OF ALLYLIC CARBONATES WITH FORMIC ACID
  188531. 1994X    4813
  188532. 4816Y
  188533. 13521
  188534. A    OGINO, T.
  188535. Tet. Lett.
  188536. PHENYLPENTACYCLO[5.3.0.0(2,5).0(3,9).0(4,8)]DECAN
  188537. ONEIN ACETIC ACID UNDERGOES H2SO4
  188538. CATALYZED REARRANGEMENT TO GIVE TWO ISOMERIC ACETOXYKETONES HAVING A NOVELTRICYCLO[5.2.1.0(4,8)]DEC
  188539. ENE RING SYSTEM BESIDES ASMALL AMOUNT OF 2,3
  188540. DIHYDRO
  188541. PHENYL
  188542. 1(8H)
  188543. AZULENONE. THE FORMATION OF THE ACETOXYKETONES CAN BEST BE ACCOUNTED BYASSUMING EQUILIBRATION OF SEVERAL STRUCTURALLY DIFFERENTNON
  188544. CLASSICAL BICYCLOBUTONIUM ION INTERMEDIATES.
  188545. 14530N
  188546. 2/28/96
  188547. CATALYZED REARRANGEMENT OF PHENYL SUBSTITUTED 1,3
  188548. BISHOMOCUBANONE VIA SEVERAL EQUILIBRATING NON
  188549. CLASSICAL BICYCLOBUTONIUM IONS
  188550. 1994X    4793
  188551. 4796Y
  188552. 13522
  188553. DELOISY, S.
  188554. Tet. Lett.C
  188555. FRUCTOSE K
  188556. STEREOSELECTIVE PREPARATION OF AN ACYCLIC ALPHA
  188557. AZIDOALDEHYDE PERMITTED ACCESS IN A FEW STEPS TO A KEYINTERMEDIATE IN A FORMAL SYNTHESIS OF MYRIOCIN.M
  188558. 14531N
  188559. 2/28/96
  188560. A_SYNTHESIS OF A
  188561. AZIDO ALDEHYDES. STEREOSELECTIVE FORMAL ACCESS to THE IMMUNOSUPPRESSANT MYRIOCIN
  188562. 1994 X    4783
  188563. 4786Y
  188564. 13523
  188565. RATOVELOMANANA, V.
  188566. Tet. Lett.C
  188567. DBU HALIDES K
  188568. A NEW PROCEDURE FOR THE SYNTHESIS OF 1
  188569. BROMOALKYNES BY DMSO/DBU INDUCED DEHYDROBROMINATION OF 1,1
  188570. DIBROMOETHYLENES UNDER MILD CONDITIONS IS DESCRIBED.M
  188571. 14532N
  188572. 2/28/96
  188573. DBU/DMSO PROMOTED DEHYDROBROMINATION OF 1,1
  188574. DIBROMOOLEFINS. A GENERAL SYNTHESIS OF 1
  188575. BROMOAROMATIC ALKYNES UNDER MILD CONDITIONS
  188576. 1994X    4777
  188577. 4780Y
  188578. 13524
  188579. SCHATZ, J.
  188580. Tet. Lett.C
  188581. ADDITIONS CARBON K
  188582. THIOBENZOPHENONE (1A) AND THIOFLUORENONE (2) SHOW HIGH DIENOPHILIC REACTIVITY AS KINETIC MEASUREMENTS DEMONSTRATEF OR A LARGER NUMBER OF DIENES.M
  188583. 14533N
  188584. 2/28/96
  188585. AzDIENOPHILIC REACTIVITY OF THE C=S BOND IN (4+2)
  188586. CYCLOADDITIONS 
  188587.  A KINETIC STUDY USING THIOBENZOPHENONE AND THIOFLUORENONE
  188588. 1994X    4767
  188589. 4770Y
  188590. 13525
  188591. DHOKTE, U. P.
  188592. Tet. Lett.C5CHIRAL HYDROBORATION MONOISOPINOCAMPHEYLBORANE AGENT 
  188593. YA NEW HYDROBORATING AGENT, 2
  188594. ISOPROPYLAPO ISOPINOCAMPHEYLBORANE ((I)PRABH(2),2F), ACHIEVES THE ASYMMETRIC HYDROBORATION OF REPRESENTATIVE PROCHIRAL ALKENES IN HIGHER OPTICAL PURITIES THAN THATACHIEVED BY THE BORANE DERIVATIVES, 2
  188595. ORGANYL APOISOPINO CAMPHEYLBORANES (R = ME, IPCBH(2);  R =ET, EAPBH(2);  AND R = PH, PAPBH(2)) PREVIOUSLY EXAMINED.
  188596. 14534N
  188597. 2/28/96
  188598. ISOPROPYLAPOISOPINOCAMPHEYLBORANE, AN IMPROVED REAGENT FOR THE ASYMMETRIC HYDROBORATION OF REPRESENTATIVE PROCHIRAL ALKENES
  188599. 1994 X    4715
  188600. 4718Y
  188601. 13526
  188602. RICHTER, L. S.
  188603. Tet. Lett.C    PEPTIDES K
  188604. THE MITSUNOBU REACTION OF N
  188605. TYROSINE METHYL EThER WITH HYDROXYMETHYL POLYSTYRENE RESIN PROCEEDS IN PRACTICALLY QUANTITATIVE YIELD IN THE PRESENCE OF ATERTIARY AMINE. COUPLING YIELDS IN THE ABSENCE OF AN AMINEARE SIGNIFICANTLY LOWER.M
  188606. 14535N
  188607. 2/28/96
  188608. AKA SURPRISING OBSERVATION ABOUT MITSUNOBU REACTIONS IN sOLID PHASE SYNTHESIS
  188609. 1994 X    4705
  188610. 4706Y
  188611. 13527
  188612. DESAI, M. C.
  188613. Tet. Lett.C)NK1 RECEPTOR CONVERSION DISCOVERY AMIDES 
  188614. INTRAMOLECULAR UREIDOMERCURATION OF BETA
  188615. AMINOACIDS SYNTHESIZED FROM APPROPRIATE BETA
  188616. LACTAMS PROVIDES AN EXPEDITIOUS ROUTE TO THE SYNTHESIS OF 2
  188617. BICYCLO[3.3.1] NONANE RING SYSTEMS. SYNTHESIS OF THE LOCKED
  188618. IN CHAIR CONFORMER 2 OF CP
  188619. 99,994 IS DESCRIBED.
  188620. 14536N
  188621. 2/28/96
  188622. A|APPLICATION OF b
  188623. LACTAMS IN THE SYNTHESIS OF SUBSTANCE P ANTAGONISTS:  PREPARATION OF 2
  188624. AZABICYCLO[3.3.1]NONANE RING SYSTEMS
  188625. 1994 X    4701
  188626. 4704Y
  188627. 13528
  188628. LIPSHUTZ, B. H.
  188629. Tet. Lett.C
  188630. ORGANIC
  188631. SYNTHESIS ACYLSILANES 
  188632. BY VIRTUE OF A TRIISOPROPYLSILYL ACYL SILANE CONTAINED WITHIN A SUBSTRATE UNDERGOING HYDROZIRCONATION, CHEMOSPECIFICITY CAN BE REALIZED FAVORING ADDITION ACROSS THE ALKENE OR ALKYNE, RATHER THAN COMPETITIVE 1,2
  188633. ADDITIONOF HYDRIDE TO THE CARBONYL PORTION OF THE MOLECULE.
  188634. 14537N
  188635. 2/28/96
  188636. AgEXPANDING THE VERSATILITY OF SCHWARTZ' REAGENT: HYDROZIRCONATION OF VINYLIC AND ACETYLENIC ACYL SILANES
  188637. 1994 X    4669
  188638. 4672Y
  188639. 13529
  188640. PEREZ, J. M.
  188641. TetrahedronCMREGIOCHEMICAL CONTROL DERIVATIVES ANTHRACYCLINONE ANTHRAQUINONES ANTIBIOTICS 
  188642. DIELS
  188643. ALDER REACTIONS OF 2,5,8(1H)
  188644. QUINOLINETRIONES WERE COMPLETELY REGIOSELECTIVE FOR ALL THE UNSYMMETRICAL DIENES TESTED, EXCEPT IN THE CASE OF ISOPRENE. THIS CORRESPONDSTO A LEVEL OF REGIOSELECTIVITY HIGHER THAN THE ONE FOUNDBY PREVIOUS WORKERS FOR 5,8
  188645. QUINOLINEQUINONE.
  188646. 14538N
  188647. 2/28/96
  188648. AKREGIOSELECTIVITY OF THE DIELS
  188649. ALDER REACTIONS OF 2,5,8(1H)
  188650. QUINOLINETRIONES
  188651. 1994 X    7923
  188652. 7932Y
  188653. 13530
  188654. GIACOMETTI, A.
  188655. TetrahedronCEDIELS
  188656. ALDER REACTIONS 2,3
  188657. DIHYDRO
  188658. DITHIINS DESULFONYLATION ETHER 
  188659. DIENOPHILES 2
  188660. METHYL
  188661. BENZODITHIIN
  188662. TETROXIDE (3A),2
  188663. PHENYL
  188664. BENZODITHIIN
  188665. TETROXIDE (3B) AND 2,3
  188666. TRIMETHYLENE
  188667. BENZODITHIIN 
  188668.  TETROXIDE (3C) HAVE BEEN PREPARED WITH DIFFERENT METHODS STARTING FROM BENZENE
  188669. DITHIOL (1). THEIR REACTIVITY WAS TESTED TOWARDS CYCLOPENTADIENE, SULFOLENE, FURAN AND 1,3
  188670. CYCLOHEXADIENE. THE DIELS
  188671. ALDER ADDUCTS TO CYCLOPENTADIENE WERE CONVERTED INTO THE CORRESPONDING UNSATURATED HYDROCARBONS, MIMICKINGTHE DIELS
  188672. ALDER REACTION OF SUBSTITUTED BLACETYLENES. THE X
  188673. RAY STRUCTURE DETERMINATIONS OF 4B, A SECONDARY PRODUCT IN
  188674. 14539N
  188675. 2/28/96
  188676. SYNTHETIC EQUIVALENTS to SUBSTITUTED ACETYLENES IN CYCLOADDITION REACTIONS. DIENOPHILIC REACTIVITY OF 2
  188677. METHYL
  188678. PHENYL
  188679.  AND 2,3
  188680. TRIMETHYLENE
  188681. BENZODITHIINS
  188682. TETROXIDES
  188683. 1994 X    7913
  188684. 7922Y
  188685. 13531
  188686. GABBUTT, C. D.
  188687. TetrahedronC
  188688. ANALOGS 
  188689. THIOCHROMAN
  188690. DIONES, WHICH RESULT FROM THE REACTION OFTHIOCHROMAN
  188691. ONES WITH ISOAMYL NITRITE, FORM FUSED HETEROCYCLES ON REACTION WITH 1,2
  188692. DIAMINES AND WITH P
  188693. ANISALDEHYDE AND AMMONIUM ACETATE. CYCLOPENTA[2][1]BENZOTHIOPYRAN
  188694. ONE, FORMED ON REACTION WITH DIBENZYL KETONE, YIELDS A DIBENZO[BD]THIOPYRAN AFTER CYCLOADDITION OF DMAD. WITH METHYL MAGNESIUM IODIDE, A MIXTURE OF THIOCHROMAN
  188695.  AND 4
  188696. OLS IF FORMED WHICH WASSEPARATED ONLY AFTER THE SELECTIVE DEHYDRATION OF THE 4
  188697. OL. THE RESULTIB)NG 4
  188698. METHYLENE DERIVATIVE WAS ISOLATED AS
  188699. 14540N
  188700. 2/28/96
  188701. A7SYNTHESIS AND REACTIVITY OF SOME THIOCHROMAN
  188702. DIONES
  188703. 1994 X    7865
  188704. 7878Y
  188705. 13532
  188706. GUIJARRO, A.
  188707. TetrahedronC
  188708. ORGANO
  188709. LITHIUM COMPOUNDS SYNTHETIC APPLICATIONS CARBONYL
  188710. COMPOUNDS BARBIER
  188711. TYPE 4,4'
  188712. BUTYLBIPHENYL
  188713. CATALYZED LITHIATION REAGENTS TRANSFORMATION DIANIONS ANIONS 
  188714. THE REACTION OF (Z) OR (E)
  188715. DICHLOROBUT
  188716. ENE (1,2) OR 3,4
  188717. DICHLOROBUT
  188718. ENE (3) WITH AN EXCESS OF LITHIUM POWDERAND A CATALYTIC AMOUNT OF 4,4'
  188719. BUTYLBIPHENYL (5MOL %) IN THE PRESENCE OF AN ELECTROPHILE [(CH2)(4)CO,BU(T)CHO,ME(3)SICL] IN THF AT 0 DEGREES C YIELDS, AFTER HYDROLYSIS, THE CORRESPONDING 1,4
  188720.  AND 1,2
  188721. DISUBSTITUTED COMPOUNDS (Z/E)
  188722. 4 AND 5, THE RATIO OF THEM BEING INDEPENDENT ON THE STARTING MATERIAL. IN THE CASE OFCOMPOUNDS 4 THE Z
  188723. DIASTEREOMER IS LARGELY THE MAJOR ONEB8.WHEN DICHLORODIETHYLSILANE WAS USED AS ELECTROPHILE THE
  188724. 14541N
  188725. 2/28/96
  188726. ARENE
  188727. CATALYSED LITHIATION OF 1,4
  188728. DICHLOROBUT
  188729. ENES AND 3,4
  188730. DICHLOROBUT
  188731. ENE AND REACTION WITH ELECTROPHILES:  A COMMON REACTION PATHWAY
  188732. 1994 X    7857
  188733. 7864Y
  188734. 13533
  188735. CABALLERO, E.
  188736. TetrahedronC
  188737. DERIVATIVES SYSTEM 
  188738. YTHE REACTION BETWEEN N
  188739. SUBSTITUTED ENAMINES AND PHENYLGLYOXAL OR GLYOXAL YIELDED DELTA(2)
  188740. PYRROLIN
  188741. ONES IN MODERATE TO GOOD YIELDS. AN UNCOMMON PYRROLO [2,1
  188742. B] THIAZOLE DERIVATIVE WAS FORMED AS A MINOR PRODUCT WHEN AN
  188743. MERCAPTOETHYL) ENAMINE WAS USED AS THE STARTING REAGENT. AN EXPLANATION FOR THE REGIOCHEMISTRY OF THEREACTION IS PROPOSED.
  188744. 14542N
  188745. 2/28/96
  188746. SUBSTITUTED PYRROLINONES FROM ENAMINES AND A
  188747. DICARBONYLS
  188748. 1994X    7849
  188749. 7856Y
  188750. 13534
  188751. SUGINOME, H.
  188752. TetrahedronC:RAY CRYSTAL
  188753. STRUCTURE RING EXPANSION PHOTOADDUCTS ALKENES 
  188754. A NEW TOTAL SYNTHESIS OF ALPHA
  188755. HIMACHALENE, A SESQUITERPNE ISOLATED FORM ESSENTIAL OIL OF A HIMALAYAN CEDAR (CEDRUSDEODARA LOUD), HAS BEEN ACHIEVED. IT IS BASED ON ASEQUENCE INVOLVING THE [2+2] PHOTOADDITION OF A CYCLICENONE WITH A SILYL ENOL ETHER, FOLLOWED BY A RADICAL
  188756. INDUCED RING EXPANSION OF THE RESULTING FUSED CYCLOBUTANOL;  THE [2+2] PHOTOADDITION OF CYCLOHEXENONEWITH 1
  188757. METHYL
  188758. TRIMETHYLSILOXY
  188759. CYCLOPENTENE IN BENZENE,FOLLOWED BY A TREATMENT OF THE RESULTING PHOTOADDUCTS WITHACID 
  188760. B-GAVE A STEREOISOMERIC MIXTURE OF 2
  188761. HYDROXY
  188762. 14543N
  188763. 2/28/96
  188764. PHOTOINDUCED MOLECULAR TRANSFORMATIONS .150. A NEW TOTAL SYNTHESIS OF (+/
  188765. HIMACHALENE BASED ON A SEQUENCE INVOLVING [2+2] PHOTOADDITION AND REGIOSELECTIVE b
  188766. SCISSION OF ALKOXYL RADICALS GENERATED FROM THE RESULTING CYCLOBUTANOLS
  188767. 1994 X    7771
  188768. 7782Y
  188769. 13535
  188770. AURICCHIO, S.
  188771. TetrahedronC
  188772. LEWIS 
  188773. TKoAROMATIC OXIMES ARE OBTAINED STEREOSPECIFICALLY BY ACTION OF NITRILE OXIDE
  188774. BF3 COMPLEXES ON AROMATIC COMPOUNDS.M
  188775. 14544N
  188776. 2/28/96
  188777. AoNITRILE OXIDE
  188778. BF3 COMPLEX AS ELECTROPHILIC MOIETY TOWARDS AROMATIC SYSTEMS:  STEREOSPECIFIC SYNTHESIS OF OXIMES
  188779. 1994 X    7589
  188780. 7596Y
  188781. 13536
  188782. MAZUMDAR, S. N.
  188783. TetrahedronC4CYCLOADDITION REACTIONS KETENES 1,3
  188784. DIAZABUTADIENES 
  188785. PHENYL
  188786. THIOALKYL
  188787. SECONDARYAMINO
  188788. DIAZA
  188789. BUTADIENES 8 YIELDED INTERESTING PYRIMIDONES 10, 22 AND 7 WITH CHLOROKETENES 2, 11 AND 12 THROUGH THEIR EPISULFONIUM INTERMEDIATES, WHEREAS 1
  188790. PHENYL
  188791. (METHYLTHIO)
  188792. DIMETHYL AMINO
  188793. DIAZA
  188794. BUTADIENES 1 GIVE DIFFERENTPYRIMIDONES WITH DIFFERENT HALOKETENES (CHLORO, BROMO ANDIODO).
  188795. 14545N
  188796. 2/28/96
  188797. ArREACTIONS OF 1,3
  188798. DIAZA
  188799. BUTADIENES WITH HALOKETENES 
  188800.  REARRANGEMENTS ACCOMPANYING [4+2] CYCLOADDITION REACTIONS
  188801. 1994 X    7579
  188802. 7588Y
  188803. 13537
  188804. ESCRIBANO, A.
  188805. TetrahedronCEEFFICIENT SYNTHESIS CYANOHYDRINS ALCOHOLS SULFOXIDES ACYLOINS IMINES 
  188806. HYDROCYANATION OF CYCLIC ALPHA
  188807. SULFINYL KETONES UNDER DIFFERENT CONDITIONS HAS BEEN STUDIED. THE OBTAINED RESULTS SHOW THAT COMPOUNDS DERIVED FROM CYCLOHEXANONE REACT WITH ET(2)ALCN YIELDING ONLY SULFINYL CYANOHYDRINSEXHIBITING DIFFERENT CONFIGURATIONS AT SULFUR AND ATHYDROXYLIC CARBON. THE STEREOSELECTIVITY IS SLIGHTLY LOWERBUT ALSO VERY HIGH STARTING FROM ALPHA
  188808. SULFINYL CYCLOPENTANONES. THE INFLUENCE OF LEWIS ACIDS AS WELL ASTHE STEREOCHEMICAL COURSE OF THESE REACTIONS HAVE ALSO BEEN DISB
  188809. CUSSED.
  188810. 14546N
  188811. 2/28/96
  188812. ADHIGHLY DIASTEREOSELECTIVE HYDROCYANATION OF A
  188813. SULFINYLCYCLOALKANONES
  188814. 1994X    7567
  188815. 7578Y
  188816. 13538
  188817. DOMINGUEZ, E.
  188818. TetrahedronCbCONJUGATE ADDITION ORGANOCOPPER REAGENTS 1,3
  188819. DIOL ACETONIDES PHENYL SULFONES DIASTEREOSELECTIVITY 
  188820. FOLLOWING AN HOMOLOGATION SEQUENCE THE READILY AVAILABLE ENANTIOMERICALLY PURE GAMMA
  188821. HYDROXY VINYL SULFONE 2 HAS BEEN TRANSFORMED, WITH COMPLETE CONTROL OF THE STEREOCHEMISTRY, INTO GAMMA
  188822. HYDROXY VINYL SULFONES OF POLYPROPIONATE STRUCTURE. THE FOUR STEREO TRIADS HAVE BEENPREPARED BY STEREOSELECTIVE ADDITIONS OF ORGANOMETALLICSTO THE VINYL SULFONE MOIETY AND BY STEREOSELECTIVE REDUCTION OF BETA
  188823. HYDROXYKETONES. IN A SIMILAR WAY, THESE TRIADS ARE THE SUBSTRATES FOR THE STEREOSELECTIVEINTRODUC
  188824. B1TION OF THE FOURTH CONSECUTIVE ASYMMETRIC CENTER.
  188825. 14547N
  188826. 2/28/96
  188827. FLEXIBLE AND STEREOSELECTIVE CONSTRUCTION OF POLYPROPIONATE CHAINS FROM ENANTIOMERICALLY PURE g
  188828. HYDROXY
  188829. UNSATURATED SULFONES
  188830. 1994 X    7557
  188831. 7566Y
  188832. 13539
  188833. Bach, K. K.B
  188834. Tetrahedron
  188835. THE PRINCIPLES OF 1,2
  188836. CYANO
  188837. HYDROXYLATION OF OLEFINS WERE APPLIED TO THE PREPARATION OF 1,2
  188838. CYANO
  188839. AMINES. THE DIPOLE COMPONENT OF THIS CYCLOADDITION WAS NITRILE IMINES, WHICH FORMED PYRAZOLINES WITH OLEFINS. RING CLEAVAGE WASACCOMPLISHED BY THERMOLYSIS OF 3
  188840. CARBOXYPYRAZOLINES, WHICH GAVE 1,2
  188841. CYANO
  188842. AMINES AND SUBSEQUENT HYDROLYSIS GAVE BETA
  188843. AMINO ACIDS. THE SYNTHESES OF THE TITLE REAGENTS WERE DESCRIBED. ETHYL 2
  188844. CHLORO
  188845.  ETHOXY
  188846. ACETATE GAVESELECTIVELY OXIMES, HYDRAZONES, NITRONES, AND PHOB;SPHONIUMSALTS WITH HYDROXYLAMINE, HYDRAZINES, N
  188847. SUBSTITUTED
  188848. 14548N
  188849. 2/28/96
  188850. DIPOLAR CYCLOADDITIONS OF ETHOXYCARBONYL
  188851. NITRILE BENZYLIMINE, ETOOC C N+
  188852.  CH2C6H5, AND SYNTHESIS OF b
  188853. AMINO ACIDS. SYNTHESIS AND REACTIONS OF ETHYL 2
  188854. CHLORO
  188855. ETHOXYACETATE AND 2
  188856. CHLORO
  188857. ETHOXYACETYL CHLORIDE
  188858. 1994 X    7543
  188859. 7556Y
  188860. 13540
  188861. ALT, M.
  188862. TetrahedronC
  188863. ENOL ETHER FORMATION RHODIUM CARBENOIDS ETHYL DIAZOACETATE DIAZO
  188864. COMPOUNDS KETONES ESTERS CYCLOPROPANATION COORDINATION ALDEHYDES 
  188865. TRANSITION
  188866. METAL
  188867. CATALYZED DECOMPOSITION OF DIAZOESTERS 2 IN THE PRESENCE OF BENZALDEHYDE, CROTONALDEHYDE, ORACETALDEHYDE GENERATES CARBONYL YLIDES WHICH CAN BE TRAPPED WITH DIMETHYL FUMARATE, DIMETHYL MALEATE, ANDDIMETHYL ACETYLENEDICARBOXYLATE TO GIVE TETRAHYDROFURANS 4,6,7, AND 8 AND DIHYDROFURAN 10, RESPECTIVELY.DECOMPOSITION OF 2A IN THE PRESENCE OF BENZALDEHYDE AND METHYL CYANOFORMATE AFFORDS NO PRODUCTS DERIVED FROM A CARBONYL YLIDE, BUT RATHER THE OXAZOLE 12. X
  188868. RAY CRYSTALSTRUCTUREB
  188869. S OF 4A AND 6 ARE PROVIDED.
  188870. 14549N
  188871. 2/28/96
  188872. TRANSITION
  188873. METAL
  188874. CATALYZED DECOMPOSITION OF DIAZO(TRIALKYLSILYL)ACETATES:  INTERMOLECULAR FORMATION AND TRAPPING OF CARBONYL YLIDES
  188875. 1994X    7435
  188876. 7444Y
  188877. 13541
  188878. AURICH, H. G.
  188879. TetrahedronCgSECONDARY ORBITAL INTERACTIONS 1,3
  188880. DIPOLAR CYCLOADDITIONS ISOXAZOLIDINES CYCLOREVERSIONS CYCLOADDITION 
  188881. IN THE 1,3
  188882. DIPOLAR CYCLOADDITION OF THE CYCLIC NITRONE ICAND THE ACYCLIC NITRONES 8A
  188883. H, 12A, B WITH DIMETHYLMALEATE IN REFLUXING CHLOROFORM NOT ONLY THE EXPECTEDCYCLOADDUCTS WITH CIS
  188884. CONFIGURATION OF THE TWO ESTERGROUPS WERE FORMED BUT ALSO SUCH WITH TRANS
  188885. CONFIGURATIONTHIS PHENOMENON IS NOT LIMITED TO CHLOROFORM, BUT WAS ALSO OBSERVED IN POLAR SOLVENTS AS CYCLOHEXANE AND N
  188886. HEXANE.HOWEVER, THERE IS NO CLUE FOR EITHER A NON
  188887. CONCERTEDREACTION COURSE OR A SUBSEQUENT CONVERSION OF THE CIS
  188888. PRODB5UCTS TO TRANS
  188889. PRODUCT, IN GENERAL. RATHER, CONVERSION
  188890. 14550N
  188891. 2/28/96
  188892. AaFORMATION OF CYCLOADDUCTS WITH TRANS
  188893. CONFIGURATED ESTER GROUPS FROM NITRONES AND DIMETHYL MALEATE
  188894. 1994 X    7417
  188895. 7434Y
  188896. 13542
  188897. SATO, T.
  188898. TetrahedronC
  188899. IRON(III) CHLORIDE OXIDATION K
  188900. COPPER(II) CHLORIDE INDUCED THE CHEMO AND REGIOSELECTIVECHLOROHYDROPEROXIDATION, AS WELL AS THE SITE
  188901. SELECTIVECHLORINATION OF OLEFINS, UNDER PHOTOOXYGENATION CONDITIONS.M
  188902. 14551N
  188903. 2/28/96
  188904. AtMETAL
  188905. CATALYZED ORGANIC PHOTOREACTIONS. CHEMO
  188906.  AND REGIOSELECTIVITIES IN THE CUCL2
  188907. INDUCED PHOTOOXIDATION OF OLEFINS
  188908. 1994 X    7375
  188909. 7384Y
  188910. 13543
  188911. CURRAN, D. P.
  188912. TetrahedronC
  188913. TRANSFER CYCLIZATION REACTIONS ALPHA
  188914. IODO ESTERS ATOM TRANSFER CHAIN
  188915. REACTIONS ALLYLATION REACTIONS ANNULATION REACTIONS RESTRICTED ROTATION ORGANIC
  188916. SYNTHESIS ROUTE ALKYLATION 
  188917. THE O
  188918. IODOANILIDE GROUP IS SHOWN TO BE BROADLY USEFUL FORTHE GENERATION AND SUBSEQUENT REACTIONS OF RADICALSADJACENT TO CARBOXYL GROUPS. THE RESULTS INDICATE THATTHIS GROUP IS ONE OF THE BEST ''PROTECTING/RADICALTRANSLOCATING'' (PRT) GROUPS INTRODUCED TO DATE. BEYONDITS GOOD PERFORMANCE IN RADICAL TRANSLOCATION REACTIONS,IT IS EASY TO INTRODUCE, SERVES AS A REASONABLE PROTECTINGGROUP BOTH BEFORE AND AFTER THE TRANSLOCATION, AND (WITHAPPROPRIATE MODIFICATIONS) IS EASY TO REMOVE.
  188919. 14552N
  188920. 2/28/96
  188921. AMIDE
  188922. BASED PROTECTING / RADICAL TRANSLOCATING (PRT) GROUPS. GENERATION OF RADICALS ADJACENT to CARBONYLS BY 1,5
  188923. HYDROGEN TRANSFER REACTIONS OF O
  188924. IODOANILIDES
  188925. 1994 X    7343
  188926. 7366Y
  188927. 13544
  188928. KAWADA, A.
  188929. SynlettC
  188930. LEWIS
  188931. ACID SC(OTF)3 M
  188932. 14553N
  188933. 2/28/96
  188934. ARSCANDIUM TRIFLUOROMETHANESULFONATE 
  188935.  A NOVEL CATALYST FOR FRIEDEL
  188936. CRAFTS ACYLATION
  188937. 1994 X
  188938. 13545
  188939. A    SINGH, V.
  188940. SynlettM
  188941. 14554N
  188942. 2/28/96
  188943. PHOTOCHEMICAL REACTIONS OF A
  188944. METHOXY
  188945. ENONES 
  188946.  ISOLATION OF 1,2
  188947. ACYL SHIFT INTERMEDIATE AND SYNTHESIS OF VERSATILE PRECURSORS to OXYGENATED CAPNELLANES
  188948. 1994 X
  188949. 13546
  188950. GORECKI, T.
  188951. SynlettC1CARCINOGEN ARYLIDENEMALONODINITRILES METABOLITES M
  188952. 14555N
  188953. 2/28/96
  188954. AuA NEW SYNTHESIS OF CYCLOPENTA[A]PHENANTHRENE INVOLVING CYCLIZATION OF 2
  188955. NAPHTHYL)
  188956. CYCLOPENTYLIDENE MALONODINITRILE
  188957. 1994 X
  188958. 13547
  188959. DUCHENE, A.
  188960. SynlettC
  188961. DIKETENE HALIDES DERIVATIVES M
  188962. 14556N
  188963. 2/28/96
  188964. SYNTHESIS OF 3
  188965. SUBSTITUTED BUT
  188966. ENOIC ACIDS VIA PALLADIUM CATALYSED CROSS
  188967. COUPLING REACTION OF 3
  188968. IODOBUT
  188969. ENOIC ACID WITH ORGANOMETALLIC REAGENTS
  188970. 1994X
  188971. 13548
  188972. MARUOKA, K.
  188973. SynlettC6ORGANIC
  188974. SYNTHESIS TRIMETHYLSILYLDIAZOMETHANE REAGENTS M
  188975. 14557N
  188976. 2/28/96
  188977. AnORGANOALUMINUM
  188978. PROMOTED DIRECT CONVERSION OF ALDEHYDES to THE HOMOLOGOUS KETONES OR OXIRANES WITH DIAZOLAKANES
  188979. 1994 X
  188980. 13549
  188981. TIETZE, L. F.
  188982. SynlettC
  188983. AMPHOTERICIN
  188984. B STRATEGY M
  188985. 14558N
  188986. 2/28/96
  188987. TANDEM
  188988. BISALKYLATION OF 2
  188989. TRIALKYLSILYL
  188990. DITHIANE 
  188991.  A NEW SEQUENTIAL TRANSFORMATION FOR THE SYNTHESIS OF C2
  188992. SYMMETRICAL ENANTIOPURE 1,5
  188993. DIOLS AND b,b'
  188994. DIHYDROXY KETONES AS WELL AS OF ENANTIOPURE 1,3,5
  188995. TRIOLS
  188996. 1994 X
  188997. 13550
  188998. TIETZE, L. F.
  188999. SynlettC
  189000. ALPHA,BETA
  189001. UNSATURATED CARBONYL
  189002. COMPOUNDS NATURAL PRODUCT SYNTHESIS LEWIS
  189003. ACID SEQUENTIAL TRANSFORMATIONS HIGH
  189004. PRESSURE DERIVATIVES 1
  189005. BUTADIENES STEREOSELECTIVITY ADDITIONS INDUCTION M
  189006. 14559N
  189007. 2/28/96
  189008. INTERMOLECULAR AND INTRAMOLECULAR HETERO
  189009. DIELS
  189010. ALDER REACTIONS .48. DENOVO SYNTHESIS OF ENANTIOPURECARBOHYDRATES 
  189011.  PREPARATION OF ETHYL b
  189012. MANNOPYRANOSIDES AND b
  189013. MANNOPYRANOSIDES BY AN ASYMMETRICALLY INDUCED HETERO
  189014. DIELS
  189015. ALDER REACTION
  189016. 1994X
  189017. 13551
  189018. KATAGIRI, T.
  189019. SynlettM
  189020. 14560N
  189021. 2/28/96
  189022. SYNTHESIS OF TRIFLUOROLACTIC ACID FROM 1,2
  189023. EPOXY
  189024. 3,3,3
  189025. TRIFLUOROPROPANE 
  189026.  ONE POT TANDEM RING OPENING OXIDATION REACTION OF EPOXIDE
  189027. 1994 X
  189028. 13552
  189029. SAMIZU, K.
  189030. SynlettM
  189031. 14561N
  189032. 2/28/96
  189033. A6AN EXPEDIENT ROUTE to INDOLE
  189034. ACETIC ACID DERIVATIVES
  189035. 1994 X
  189036. 13553
  189037. ISIMARU, K.
  189038. SynlettC8ALPHA
  189039. HYDROGENS BORON REAGENT IMINES ORGANOCOPPER DIENE M
  189040. 14562N
  189041. 2/28/96
  189042. AtSTEREOCONTROL IN [4+2] TYPE CYCLOADDITION OF AN ALDIMINE DERIVED FROM (S)
  189043. ETHYL LACTATE WITH 2
  189044. SILOXY
  189045. BUTADIENES
  189046. 1994X
  189047. 13554
  189048. LOVE, B. E.
  189049. SynlettC
  189050. DIELS
  189051. ALDER REACTIONS 4
  189052. PI PARTICIPATION ALDEHYDES SULFONAMIDES IMINES 1
  189053. BUTADIENES SULFONYLIMINES TOSYLIMINES CONVENIENT INSITU 
  189054. TOSYL IMINE SULFONYL PREPARATION SYNTHESIS CONDITIONS SULFONAMIDE LEWIS ACID SILICATE NEUTRAL HINDERED STERICM
  189055. 14563N
  189056. 2/28/96
  189057. PREPARATION OF N
  189058. TOSYLALDIMINES
  189059. 1994 X
  189060. 13555
  189061. SAA, C.
  189062. SynlettCTACID DERIVATIVES 2,3
  189063. DOUBLE BOND ALKYNES CONSTRUCTION CYCLIZATION CHEMISTRY NUCLEUS M
  189064. 14564N
  189065. 2/28/96
  189066. A\A COBALT
  189067. CATALYZED ENTRY INTO THE ERGOT ALKALOIDS 
  189068.  TOTAL SYNTHESES OF 
  189069. LYSERGENE AND 
  189070. 1994 X
  189071. 13556
  189072. NISHIKAWA, T.
  189073. SynlettC&REARRANGEMENT CATALYSIS CHLORIDE RING M
  189074. 14565N
  189075. 2/28/96
  189076. ABONE POT SYNTHESIS OF HALOACETYLENES FROM TRIMETHYLSILYl ACETYLENES
  189077. 1994 X
  189078. 13557
  189079. NISHIKAWA, T.
  189080. SynlettC$DYNEMICIN DNA CHEMISTRY ANALOG CORE M
  189081. 14566N
  189082. 2/28/96
  189083. AMCESIUM FLUORIDE PROMOTED CYCLIZATION IN THE SYNTHESIS OF ENEDIYNE ANTIBIOTICS
  189084. 1994 X
  189085. 13558
  189086. CAMPORA, J.
  189087. SynlettC
  189088. METALLACYCLIC ALKENYLKETONE COMPLEXES MOLECULAR
  189089. STRUCTURE CARBON
  189090. MONOXIDE X
  189091. RAY METHYLNICKEL COMPOUNDS THERMAL
  189092. DECOMPOSITION INSERTION CHEMISTRY CRYSTAL
  189093. STRUCTURE THIONE ANALOGS NICKEL M
  189094. 14567N
  189095. 2/28/96
  189096. AfORGANONICKEL CHEMISTRY IN ORGANIC SYNTHESIS 
  189097.  SOME APPLICATIONS OF ALKYL AND METALLACYCLIC DERIVATIVES
  189098. 1994 X
  189099. 13559
  189100. TORU, T.
  189101. 14568N
  189102. 2/28/96
  189103. A4VINYL ANION AND ACETYLIDE EQUIVALENTS WITH FUNCTIONS
  189104. 1994 X
  189105. 13560
  189106. KIRA, M.
  189107. HYPERCOORDINATE ORGANOSILICON COMPOUNDS ORGANIC SYNTHESIS REGIOSPECIFIC ALLYLATION DIASTEREOSELECTIVE CROTYLATION HYDRIDOSILICATES SILYLSILICATES OXIDATIVE SI
  189108. C CLEAVAGE TRANSITION STRUCTURE ABINITIO MO STUDY HIGHLY STEREOSELECTIVE ALLYLATION M
  189109. 14569N
  189110. 2/28/96
  189111. A_CHARACTERISTICS OF HYPERCOORDINATE SILICON COMPOUNDS AND THEIR APPLICATION to ORGANIC SYNTHESIS
  189112. 1994 X
  189113. 13561
  189114. FUJIWARA, T.
  189115. CYCLOBUTENYL KETONE 2
  189116. PHENYLTHIOCYCLOBUTYL KETONE HYDRINADANONE CYCLOOCTATRIENE ACETYLCYCLOHEXENE ENOL SILYL ETHER TRISUBSTITUTED OLEFIN [2+2]CYCLOADDITION RING ENLARGEMENT REACTION RING OPENING REACTION M
  189117. 14570N
  189118. 2/28/96
  189119. A2ORGANIC SYNTHESIS UTILIZING 1
  189120. CYCLOBUTENYL KETONES
  189121. 1994 X
  189122. 13562
  189123. HAYASHI, M.
  189124. ENANTIOSELECTIVE REACTION SCHIFF BASE TITANIUM ALKOXIDE TRIMETHYLSILYL CYANIDE SILYLCYANATION CYANOHYDRIN DIKETENE 5
  189125. HYDROXY
  189126. OXOESTER COMPACTIN MEVINOLIN M
  189127. 14571N
  189128. 2/28/96
  189129. AkASYMMETRIC CARBON
  189130. CARBON BOND FORMING REACTIONS CATALYZED BY CHIRAL SCHIFF BASE
  189131. TITANIUM ALKOXIDE COMPLEXES
  189132. 1994 X
  189133. 13563
  189134. pA    Oh, S. H.B
  189135. 14572N
  189136. 2/28/96
  189137. METAL
  189138. CATALYZED ORGANIC PHOTOREACTIONS. PHOTOREACTION OF 2
  189139. CHLOROACETOPHENONE WITH FUNCTIONALIZED OLEFINS IN THE PRESENCE OF SILVER TRIFLUOROMETHANESULFONATE
  189140. 1994X    3744
  189141. 3746Y
  189142. 13564
  189143. KRIKORIAN, S. E.
  189144. 14573N
  189145. 2/28/96
  189146. AKTRIIODOETHYLENE:  A PRODUCT OF THE THERMAL DECOMPOSITION OF DIIODOACETYLENE
  189147. 1994X    3742
  189148. 3743Y
  189149. 13565
  189150. UDDING, J. H.
  189151. 14574N
  189152. 2/28/96
  189153. ApXANTHATE TRANSFER ADDITION OF A GLYCINE RADICAL EQUIVALENT to ALKENES. A NOVEL ROUTE to A
  189154. AMINO ACID DERIVATIVES
  189155. 1994X    3721
  189156. 3725Y
  189157. 13566
  189158. METZ, P.
  189159. 14575N
  189160. 2/28/96
  189161. AySTEREOSELECTIVE SYNTHESIS OF SUBSTITUTED CYCLOHEXENOLS FROM A FURAN
  189162. DERIVED SULTONE VIA TANDEM ELIMINATION / 1,6
  189163. ADDITION
  189164. 1994 X    3687
  189165. 3689Y
  189166. 13567
  189167. A    PU, Y. L.
  189168. ALPHA
  189169. AMINO
  189170. ACIDS PSEUDOMONAS
  189171. FLUORESCENS PARA
  189172. AMINOPHENYLALANINE STEREOSELECTIVE SYNTHESIS CHIRAL GLYCINE OBAFLUORIN OXAZOLOMYCIN BIOSYNTHESIS DESIGN ENTEROBACTINM
  189173. 14576N
  189174. 2/28/96
  189175. AdSYNTHESIS, STABILITY, AND ANTIMICROBIAL ACTIVITY OF (+)
  189176. OBAFLUORIN AND RELATED b
  189177. LACTONE ANTIBIOTICS
  189178. 1994 X    3642
  189179. 3655Y
  189180. 13568
  189181. KITTAKA, A.
  189182. BICYCLIC NUCLEOSIDES ANGULAR TRIQUINANES (+)
  189183. HYDANTOCIDIN CONSTRUCTION RIBOSE RING PHOTOCYCLIZATION STEREOISOMERS HYDANTOCIDIN DERIVATIVES M
  189184. 14577N
  189185. 2/28/96
  189186. VINYL RADICAL
  189187. BASED CYCLIZATION OF B
  189188. SUBSTITUTED 1
  189189. DEOXY
  189190. ERYTHRO
  189191. ENO FURANOSYL) URACILS:  SYNTHESIS OF ANOMERIC SPIRO NUCLEOSIDES
  189192. 1994X    3636
  189193. 3641Y
  189194. 13569
  189195. MAK, C. C.
  189196. JOCC`LIGANDS BOND 
  189197. FISCHER CARBENE COMPLEX ALLYL SILANE CARBENOID 2+1 INTRODUCTION ANNULATION WRITINGM
  189198. 14578N
  189199. 2/28/96
  189200. Aj[2+1] CARBENOID INSERTION REACTION OF FISCHER CARBENE COMPLEXES WITH SILANES:  A SYNTHESIS OF ALLYLSILANES
  189201. 1994 X    3585
  189202. 3589Y
  189203. 13570
  189204. COOK, G. R.
  189205. GLYCOSIDASE INHIBITORS STEREOSELECTIVE SYNTHESIS ORGANOCOPPER REAGENTS PIPERIDINE ALKALOIDS PRACTICAL SYNTHESIS PYRIDINE ALKALOIDS CELL RECOGNITION HIGHER
  189206. ORDER PYRROLIDINE CHEMISTRY M
  189207. 14579N
  189208. 2/28/96
  189209. CONSTRUCTION OF HYDROXYLATED ALKALOIDS (+/
  189210. MANNONOLACTAM, (+/
  189211. DEOXYMANNOJIRIMYCIN, AND (+/
  189212. PROSOPININE THROUGH AZA
  189213. ANNULATION
  189214. 1994 X    3575
  189215. 3584Y
  189216. 13571
  189217. RENAUD, P.
  189218. JOCCbADDITION
  189219. REACTIONS SUBSTITUTED RADICALS VINYL CYCLOPROPANES STEREOSELECTIVITY SULFOXIDES REAGENTS M
  189220. 14580N
  189221. 2/28/96
  189222. AxALTERING THE STEREOCHEMISTRY OF ALLYLATION REACTIONS OF CYCLIC A
  189223. SULFINYL RADICALS:  EFFECTS OF SOLVENTS AND LEWIS ACIDS
  189224. 1994 X    3547
  189225. 3552Y
  189226. 13572
  189227. GRAVEN, A.
  189228. JOCC&LIGAND TRANSFER ALKYL RADICALS HALIDESM
  189229. 14581N
  189230. 2/28/96
  189231. ABOXIDATIVE HALO
  189232. DECARBOXYLATION OF A,b
  189233. UNSATURATED CARBOXYLIC ACIDS
  189234. 1994X    3543
  189235. 3546Y
  189236. 13573
  189237. WARM, A.
  189238. 14582N
  189239. 2/28/96
  189240. AYON THE FORMATION OF (SULFONYLAMINO)SULFONYL ISOCYANATES AND (ARYLOXY)SULFONYL ISOCYANATES
  189241. 1994 X    3540
  189242. 3542Y
  189243. 13574
  189244. HOFFMAN, R. V.
  189245. VERSATILE AMIDOALKYLATION REAGENTS SULFONYLATED HYDROXAMIC ACIDS INTRAMOLECULAR REACTIONS REGIOSELECTIVE REDUCTION NITROGEN REARRANGEMENTS ARYLSULFONYLOXY AMINES CATIONIC CARBON NUCLEOPHILES ROUTE RING M
  189246. 14583N
  189247. 2/28/96
  189248. A FACILE PREPARATION OF N
  189249. (ISOPROPOXYALKYL) AMIDES BY GENERATION and TRAPPING OF N
  189250. ACYLIMINIUM IONS FROM IONIZATION
  189251. REARRANGEMENT REACTIONS OF N
  189252. TRIFLYLOXY AMIDESE
  189253. 1994X    3530
  189254. 3539Y
  189255. 13575
  189256. MARSHALL, J. A.
  189257. JOCC,SECONDARY ALCOHOLS ALDEHYDES ALLYLSTANNANES M
  189258. 14584N
  189259. 2/28/96
  189260. SYNTHESIS OF SYN and ANTI HOMOPROPARGYLIC and ALLENIC ALCOHOLS THROUGH DIASTEREOSELECTIVE SE2' ADDITION OF A COMMON CHIRAL ALLENYL STANNANE PRECURSOR to ALDEHYDES
  189261. 1994X    3509
  189262. 3511Y
  189263. 13576
  189264. SONAWANE, H. R.
  189265. Ind. J. Chem. Sect. BM
  189266. 14585N
  189267. 2/28/96
  189268. AIAN EFFICIENT SYNTHESIS OF FENOPROFEN, AN IMPORTANT ANTIINFLAMMATORY AGENT
  189269. 1994X
  189270. 13577
  189271. NAIDU, M. S. R.
  189272. Ind. J. Chem. Sect. BC
  189273. SULFONESM
  189274. 14586N
  189275. 2/28/96
  189276. ARCYCLOPROPANATION OF SOME UNSATURATED KETOSULPHONES WITH CARBONYL STABILIZED YLIDES
  189277. 1994X
  189278. 13578
  189279. DUTTA, D. K.
  189280. Ind. J. Chem. Sect. BC
  189281. BENZISOXAZOLES REDUCTIONM
  189282. 14587N
  189283. 2/28/96
  189284. ATA CONVENIENT METHOD FOR THE PRODUCTION OF ORTHO
  189285. AMINO and N
  189286. ALKYLAMINO BENZOPHENONES
  189287. 1994 X
  189288. 13579
  189289. YELAMAGGAD, C. V.
  189290. Ind. J. Chem. Sect. BM
  189291. 14588N
  189292. 2/28/96
  189293. REACTIONS OF 4
  189294. THIAZOLYL)SYDNONES IN ACID MEDIA 
  189295.  SYNTHESIS OF 3
  189296. DIMETHYLPHENYLPYRAZOL
  189297. YL)THIAZOL
  189298. YL] SYDNONES
  189299. 1994 X
  189300. 13580
  189301. A    JOSHI, N.
  189302. Ind. J. Chem. Sect. BM
  189303. 14589N
  189304. 2/28/96
  189305. AsSYNTHESIS OF IMIDAZOLINONES, AZETIDINONES and FORMAZANS FROM HYDRAZINO
  189306. TRIAZINES AS POTENTIAL ANTIMICROBIALAGENTS
  189307. 1994 X
  189308. 13581
  189309. KHAN, M. N.
  189310. Ind. J. Chem. Sect. BC
  189311. BASE CATALYSIS IONIZED PHENYL SALICYLATE RATE
  189312. DETERMINING STEP GENERAL ACID SECONDARY
  189313. AMINES ALKALINE
  189314. HYDROLYSIS MECHANISM KINETICS AMINOLYSIS CLEAVAGE M
  189315. 14590N
  189316. 2/28/96
  189317. EVIDENCE FOR THE OCCURRENCE OF N
  189318. SUBSTITUTED PHTHALIMIDES AS INTERMEDIATES IN THE REACTIONS OF N
  189319. ETHOXYCARBONYLPHTHALIMIDE WITH PRIMARY AMINES
  189320. 1994X
  189321. 13582
  189322. Pal, R.B
  189323. Ind. J. Chem. Sect. BM
  189324. 14591
  189325. 2/28/96
  189326. HETEROCYCLIC SYSTEMS CONTAINING BRIDGEHEAD NITROGEN ATOM. 75. SYNTHESES OF THIAZOLO[2,3
  189327. B] BENZO[H]QUINAZOLINE and [1,3]THIAZINO[2,3
  189328. B]BENZO[H]QUINAZOLINE
  189329. 1994X
  189330. 13583
  189331. SHARMA, S. D.
  189332. Ind. J. Chem. Sect. BC9STEREOSPECIFIC SYNTHESIS STEREOSELECTIVITY CYCLOADDITION M
  189333. 14592N
  189334. 2/28/96
  189335. AFSYNTHESIS and MECHANISM OF FORMATION OF b
  189336. LACTAMS FROM N
  189337. METHYL IMINES
  189338. 1994X
  189339. 13584
  189340. GRIFFITHS, S. L.
  189341. Pure Appl. Chem.C
  189342. CHROMIUM
  189343. TRICARBONYL COMPLEXES SULFINYL
  189344. CONTROLLED FORMATION ASYMMETRIC
  189345. SYNTHESIS STEREOSELECTIVE SYNTHESIS ORGANIC
  189346. SYNTHESIS PLANAR CHIRALITY ALDOL REACTION ALCOHOLS M
  189347. 14593N
  189348. 2/28/96
  189349. AASULFOXIDES and STEREOCHEMICAL CONTROL IN ORGANOMETALLIC CHEMISTRY
  189350. 1994X    1565
  189351. 1572Y
  189352. 13585
  189353. SUZUKI, K.
  189354. Pure Appl. Chem.CbC
  189355. ARYL GLYCOSIDES O
  189356. GLYCOSIDE REARRANGEMENT ALDEHYDE HYDROZIRCONATION CP2HFCL2
  189357. AGCLO4 CHLORIDE M
  189358. 14594N
  189359. 2/28/96
  189360. A/NOVEL LEWIS ACID CATALYSIS IN ORGANIC SYNTHESIS
  189361. 1994X    1557
  189362. 1564Y
  189363. 13586
  189364. A    MURAI, S.
  189365. Pure Appl. Chem.C_TRANSITION
  189366. METAL COMPLEXES H BONDS ACTIVATION ALKANES CYCLOMETALATION CHEMISTRY NITROGEN ALKYL M
  189367. 14595N
  189368. 2/28/96
  189369. CATALYTIC C
  189370. H OLEFIN COUPLING
  189371. 1994X    1527
  189372. 1534Y
  189373. 13587
  189374. A    LU, X. Y.
  189375. Pure Appl. Chem.C
  189376. STEREOSPECIFIC HYDROHALOGENATION REACTION CATALYZED STEREOSELECTIVE SYNTHESIS RADICAL CYCLIZATION PALLADIUM DERIVATIVES 2
  189377. ALKYNOATES LACTONES STEREOCHEMISTRY MECHANISM ENYNESM
  189378. 14596N
  189379. 2/28/96
  189380. AKCONSTRUCTION OF A
  189381. ALKYLIDENE
  189382. BUTYROLACTONES FROM ACYCLIC ESTER PRECURSORS
  189383. 1994X    1501
  189384. 1508Y
  189385. 13588
  189386. LIPSCHUTZ, B. H.
  189387. Pure Appl. Chem.CUORGANIC
  189388. SYNTHESIS HYDROZIRCONATION TRANSMETALATION VINYLSTANNANES ALKYLATION REAGENT M
  189389. 14597N
  189390. 2/28/96
  189391. AINEW SYNTHETIC METHODS BASED ON ORGANOZIRCONIUM and ORGANOCOPPER CHEMISTRY
  189392. 1994 X    1493
  189393. 1500Y
  189394. 13589
  189395. KOGA, K.
  189396. Pure Appl. Chem.C
  189397. TRIMETHYLSILYL ENOL ETHERS ACTIVE 3
  189398. KETO STEROIDS LITHIUM AMIDE BASES BETA
  189399. ESTERS ENANTIOSELECTIVE DEPROTONATION 4
  189400. SUBSTITUTED CYCLOHEXANONES ALKYLATION DIALKYLAMIDES BROMIDE AMINE M
  189401. 14598N
  189402. 2/28/96
  189403. A/ASYMMETRIC SYNTHESIS MEDIATED BY CHIRAL LIGANDS
  189404. 1994 X    1487
  189405. 1492Y
  189406. 13590
  189407. HIYAMA, T.
  189408. Pure Appl. Chem.C0ORGANOSILICON COMPOUNDS ORGANIC HALIDES REAGENT M
  189409. 14599N
  189410. 2/28/96
  189411. AdPALLADIUM
  189412. CATALYZED CROSS
  189413. COUPLING REACTION OF ORGANOMETALLOIDS THROUGH ACTIVATION WITH FLUORIDE ION
  189414. 1994X    1471
  189415. 1478Y
  189416. 13591
  189417. VANKOTEN, G.
  189418. Pure Appl. Chem.C3ORGANOMETALLIC CHEMISTRY CRYSTAL
  189419. STRUCTURE CLUSTER M
  189420. 14600N
  189421. 2/28/96
  189422. A<ASYMMETRIC CATALYSIS WITH CHIRAL ORGANOCOPPER ARENETHIOLATES
  189423. 1994X    1455
  189424. 1462Y
  189425. 13592
  189426. SCHLOSSER, M.
  189427. Pure Appl. Chem.C
  189428. ORGANIC
  189429. SYNTHESIS STEREOSPECIFIC SYNTHESIS DIRECTED METALATION WITTIG REACTION ALPHA
  189430. SANTALOL BASES DERIVATIVES REAGENTS HYDROZIRCONATION LITHIATION M
  189431. 14601
  189432. 2/28/96
  189433. AnSITE SELECTIVE HYDROGEN METAL EXCHANGE 
  189434.  COMPETITION and COOPERATION BETWEEN SUPERBASES and NEIGHBORING GROUPS
  189435. 1994X    1439
  189436. 1446Y
  189437. 13593
  189438. SAKURAI, H.
  189439. Pure Appl. Chem.C
  189440. BENZENE DIANION M
  189441. 14602N
  189442. 2/28/96
  189443. ATAN APPROACH to STABLE ORGANIC MOLECULES OF THE TRIPLET STATE VIA ORGANOSILICON ROUTE
  189444. 1994 X    1431
  189445. 1438Y
  189446. 13594
  189447. OVERMAN, L. E.
  189448. Pure Appl. Chem.
  189449. C{SCOPADULCIC ACID
  189450. B SCOPARIA
  189451. DULCIS L PRACTICAL SYNTHESIS SPIROOXINDOLES CONSTRUCTION REDUCTION HALIDES KETONES BORANE RING M
  189452. 14603N
  189453. 2/28/96
  189454. APPLICATION OF INTRAMOLECULAR HECK REACTIONS FOR FORMING CONGESTED QUATERNARY CARBON CENTERS IN COMPLEX MOLECULE TOTAL SYNTHESIS
  189455. 1994 X    1423
  189456. 1430Y
  189457. 13595
  189458. LEY, S. V.
  189459. Pure Appl. Chem.CMANTIBIOTIC CP
  189460. 61,405 ROUTIENNOCIN ALLYL TRICARBONYLIRON TETRAHYDROFURAN ACID M
  189461. 14604N
  189462. 2/28/96
  189463. A6TRICARBONYLIRON LACTONE COMPLEXES IN ORGANIC SYNTHESIS
  189464. 1994 X    1415
  189465. 1422Y
  189466. 13596
  189467. JABUR, F. A.
  189468. J.C.S. Chem. Commun.M
  189469. 14605N
  189470. 2/28/96
  189471. A.PINACOL REARRANGEMENT ON SAPO MOLECULAR SIEVES
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  189475. LUCCHINI, V.
  189476. J.C.S. Chem. Commun.C
  189477. ANIONOTROPIC REARRANGEMENTS DIASTEREOSELECTIVE ADDITION CATALYSTS 1,1'
  189478. BINAPHTHALENE
  189479.  2,2'
  189480. DIOL METHOXYSELENENYLATION ENANTIOSELECTIVITY AZIRIDINATION SUBSTITUTION RESOLUTION REAGENTSM
  189481. 14606N
  189482. 2/28/96
  189483. ENANTIOPURE THIOSULFONIUM SALTS IN ASYMMETRIC SYNTHESIS. FACE SELECTIVITY IN ELECTROPHILIC ADDITIONS to UNFUNCTIONALISED OLEFINS
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  189486. 13598
  189487. BAILEY, P. D.
  189488. J.C.S. Chem. Commun.
  189489. C4PICTET
  189490. SPENGLER REACTION TETRAHYDRO
  189491. CARBOLINES M
  189492. 14607N
  189493. 2/28/96
  189494. NEW ASYMMETRIC ROUTE to BRIDGED INDOLE ALKALOIDS:  FORMAL SYNTHESES OF (
  189495. SUAVEOLINE, (
  189496. RAUMACLINE and (
  189497. METHYLRAUMACLINE
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  189499. 1560Z
  189500. 13599
  189501. KUBOTA, Y.
  189502. J.C.S. Chem. Commun.C3AROMATIC POLYAMIDES CARBON
  189503. MONOXIDE DIAMINES BASES M
  189504. 14608N
  189505. 2/28/96
  189506. ApAN EFFICIENT SYNTHESIS OF 2,6
  189507. BUTYLPHENYL ESTERS BY PALLADIUM
  189508. CATALYSED CARBONYLATION OF 4
  189509. BROMOBIPHENYL
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  189511. 1554Z
  189512. 13600
  189513. MAGNUS, P.
  189514. J.C.S. Chem. Commun.C
  189515. CLEAVAGE SUBUNIT ROUTE M
  189516. 14609N
  189517. 2/28/96
  189518. A?A CONCISE SYNTHESIS OF THE ANTHRAQUINONE PORTION OF DYNEMICIN A
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  189520. 1546Z
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  189522. MAGNUS, P.
  189523. J.C.S. Chem. Commun.CAANTITUMOR ANTIBIOTICS ESPERAMICIN
  189524. A1 CALICHEAMICIN
  189525. GAMMA
  189526. 1 SALTS M
  189527. 14610N
  189528. 2/28/96
  189529. AWSHORT SYNTHESIS OF THE DYNEMICIN CORE STRUCTURE:  UNUSUAL BRIDGEHEAD ENOLATE REACTIVITY
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  189533. MAGNUS, P.
  189534. J.C.S. Chem. Commun.CUCALICHEAMICIN
  189535. ESPERAMICIN ANALOGS ANTITUMOR ANTIBIOTICS ENEDIYNE CYCLIZATION TRIGGER M
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  189537. 2/28/96
  189538. AvRELATIVE RATES OF CYCLOAROMATIZATION OF DYNEMICIN AZABICYCLO[7.3.1] ENEDIYNE CORE STRUCTURES. AN UNUSUAL CHANGE IN d S
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  189545. ALDER ISOINDOLE HETEROCYCLE SYNTHESIS EXCHANGEM
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  189547. 2/28/96
  189548. ADA NEW ROUTE to THE ISOINDOLE NUCLEUS VIA FURAN
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  189550. EXCHANGE
  189551. 1994 X
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  189553. 13604
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  189555. FRASER REID B
  189556. J.C.S. Chem. Commun.C
  189557. CLOSURE FORCE
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  189559. CHEMOSELECTIVITY RADICAL CYCLIZATION WRITING INTRODUCTION COMPETITION SELECTIVITY SUGAR CARBOHYDRATE INTRAMOLECULARM
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  189561. 2/28/96
  189562. FINE TUNING OF CHEMO
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  189565. ERYTHRO
  189566. DIENOPYRANOSIDES. STEREOSELECTIVE ACCESS to CARBOCYCLES and BRANCHED
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  189573. ELECTROCHEMICAL OXIDATION ORGANOSILICON COMPOUNDS HETEROATOM COMPOUNDS ELECTRON
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  189575. OXIDATION AMMONIUM
  189576. NITRATE PHENYL SULFIDES CATION RADICALS CYCLIZATION GENERATION M
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  189578. 2/28/96
  189579. ApTANDEM OXIDATIVE RING CLEAVAGE CYCLISATION REACTIONS OF CYCLOPROPYLSULFIDES:  A NOVEL SYNTHESIS OF CYCLIC ETHERS
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  189584. J.C.S. Chem. Commun.C
  189585. ORGANIC
  189586. SYNTHESIS MANGANESE(III) ACETATE IPSO SUBSTITUTION ACID
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  189589. 2/28/96
  189590. AK1,5 VS 1,6 INTRAMOLECULAR HOMOLYTIC AROMATIC SUBSTITUTION BY VINYL RADICALS
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  189598. AZTHE SYNTHESIS OF HETEROCYCLES FROM INDOLIN
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  189605. AMINES M
  189606. 14617N
  189607. 2/28/96
  189608. CYCLOHEXYLIDENEACETYL ISOTHIOCYANATE 
  189609.  PRECURSOR FOR THE SYNTHESIS OF 1,3
  189610. THIAZASPIROCYCLOALKANES and 1,3
  189611. DIAZASPIROCYCLOALKANES
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  189619. AgPREPARATION and SPECTROSCOPIC PROPERTIES OF SPIROCYCLIC 1
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  189622. TETRAARYL
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  189630. 2/28/96
  189631. AKSYNTHESIS OF SOME 2
  189632. (SUBSTITUTED THIO) PYRIDINES and THIENO[2,3
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  189638. ELECTROPHILIC AMINATION LITHIUM TERT
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  189640. TOSYLOXYCARBAMATE CHLOROMAGNESIUM TERT
  189641. BUTYL N
  189642. TOSYLOXYCARBAMATE ALKYLLITHIUM LITHIO DIALKYLCUPRATE ARYLOCOPPER N
  189643. PROTECTED PRIMARY AMINE DISPLACEMENTS ALKOXYAMINES REAGENTS M
  189644. 14620N
  189645. 2/28/96
  189646. ATELECTROPHILIC AMINATION OF CARBANIONS WITH METALLATED TERT
  189647. BUTYL N
  189648. TOSYLOXYCARBAMATE
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  189652. Bull. Soc. Chim. Fr.CsAMINO ALCOHOL OXAZINE THREITOL CHIRAL AUXILIARIES AMINO
  189653. ALCOHOLS REDUCTION DERIVATIVES AUXILIARIES HYDRIDE ANALOGS M
  189654. 14621N
  189655. 2/28/96
  189656. AKCHIRAL 1,3
  189657. AMINO ALCOHOLS and TETRAHYDRO
  189658. OXAZINES DERIVED FROM THREITOL
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  189663. ALLENES CARBOPALLADATION PI
  189664. ALLYL PALLADIUM 1,3
  189665. DIENE CYCLIZATION AROMATIC COMPOUNDS FUNCTIONALIZED STYRENES HYDROCARBONS PALLADIUM DERIVATIVES M
  189666. 14622N
  189667. 2/28/96
  189668. AATRISUBSTITUTED BENZOATE SYNTHESIS VIA CARBOPALLADATION OF ALLENES
  189669. 1994X
  189670. 13614
  189671. GRISSOM
  189672. JOCCK ALLENE ALKYNE SIGMATROPIC COPE ENYNE DIRADICAL BERGMAN RADICAL CYCLIZATIONM
  189673. 14623N
  189674. 2/28/96
  189675. AJTANDEM ENYNE ALLENE RADICAL CYCLIZATION VIA 3,3
  189676. SIGMATROPIC REARRANGEMENTS
  189677. 1994X
  189678. 5114Y
  189679. 13615
  189680. LEAHY 
  189681. JOCC_CYCLOPENTANONE 3,3
  189682. DISUBSTITUTED CUPRATE ADDITION CONJUGATE ALTERNATIVE METHOD ANNULATION NOVELM
  189683. 14624N
  189684. 2/28/96
  189685. AOCONVENIENT CONSTRUCTION OF CYCLOPENTANONES VIA CYCLOPENTANNULATION OF CARBONYLS
  189686. 1994X
  189687. 5496Y
  189688. 13616
  189689. A    DE KIMPE 
  189690. JOCCM FURAN ELECTROPHILE INDUCED CYCLIZATION TETRAHYDROFURAN ALKENE INTRAMOLECULARM
  189691. 14625N
  189692. 2/28/96
  189693. A^SYNTHESIS OF FUNCTIONALIZED TETRAHYDROFURANS BY ELECTROPHILE INDUCED CYCLIZATION OF 4
  189694. ALKENALS
  189695. 1994X
  189696. 5485Y
  189697. 13617
  189698. SNIDER 
  189699. CzRADICAL TARGET 2+2 KETENE CYCLOBUTANONE MANGANESE COPPER VINYL ALCOHOL REARRANGEMENT CYCLIZATION RING OPENING CYCLOBUTANOLM
  189700. 14626N
  189701. 2/28/96
  189702. TOTAL SYNTHESIS OF A SILPHIPERFOLANE DERIVATIVE VIA AN INTRAMOLECULAR 2+2 KETENE CYCLOADDITION FOLLOWED BY A MANGANESE RADICAL INDUCED CYCLIZATION
  189703. 1994X
  189704. 5419Y
  189705. 13618
  189706. MARGARETHA 
  189707. JOCCOENONE PHOTOCHEM VINYL CARBENE CYCLOADDITION FURAN CYCLIZATION BUTADIENYL AGOSTAM
  189708. 14627N
  189709. 2/28/96
  189710. AYFURANS FROM NOVEL 3+2 PHOTOCYCLOADDITION OF ALKENES to ALKYNYL SUBSTITUTED CYCLOHEXENONES
  189711. 1994X
  189712. 5393Y
  189713. 13619
  189714. A    FUKUMOTO 
  189715. JOCC'RADICAL CYCLIZATION TIN TARGET ALKALOIDM
  189716. 14628N
  189717. 2/28/96
  189718. AHASYMMETRIC TOTAL SYNTHESIS OF ALKALOID TACAMONINE BY RADICAL CYCLIZATION
  189719. 1994X
  189720. 5317Y
  189721. 13620
  189722. WENTRUP
  189723. JOCC= OXA KETENE REARRANGEMENT 1,3
  189724. SHIFT IMINE CYCLOADDITION FLASHM
  189725. 14629N
  189726. 2/28/96
  189727. AUKETENE
  189728. KETENE REARRANGEMENT SUBSTITUENT EFFECTS ON THE 1,3
  189729. MIGRATION IN A-OXO KETENES
  189730. 1994X
  189731. 5279Y
  189732. 13621
  189733. A    FURSTNER 
  189734. JOCCVDICARBONYL COUPLING TITANIUM REDUCTIVE MCMURRY ESTER INDOLE METHOD COURSE DIMERIZATIONM
  189735. 14630N
  189736. 2/28/96
  189737. SITE SELECTIVE FORMATION OF LOW VALENT TITANIUM REAGENTS.  AN INSTANT PROCEDURE FOR THE REDUCTIVE COUPLING OF OXO AMIDES to INDOLES
  189738. 1994X
  189739. 5215Y
  189740. 13622
  189741. A    DE KIMPE 
  189742. JOCCTCYCLOADDITION ENAMINES AZIDE TRIAZOLINE RETRO CYCLOREVERSION DIAZO CONVERSION DIPOLEM
  189743. 14631N
  189744. 2/28/96
  189745. AXSYNTHESIS OF b-LACTAM DERIVATIVES BY CYCLOADDITION OF 2
  189746. METHYLENE AZETIDINES WITH AZIDES
  189747. 1994X
  189748. 5189Y
  189749. 13623
  189750. MEYERS
  189751. JOCCX ENONE ALLYL SILANE CATION REARRANGEMENT 1,2
  189752. SILYL SHIFT 2+2 3+2 DANHEISER CHIRAL LACTAMM
  189753. 14632N
  189754. 2/28/96
  189755. AO3+2 CYCLOADDITIONS OF TRIISOPROPYL ALLYL SILANE to UNSATURATED BICYCLIC LACTAMS
  189756. 1994X
  189757. 5144Y
  189758. 13624
  189759. A    SIMPKINS 
  189760. JOCC]EPISULFONE CARBANION SILYLATION RAMBERG BACKLUND EXTRUSION SO2 HALO SULFONE SILYLATED SILICONM
  189761. 14633N
  189762. 2/28/96
  189763. AKFIRST EXAMPLES OF EPISULFONE REACTIONS VIA SULFONYL CARBANION INTERMEDIATES
  189764. 1994X
  189765. 5141Y
  189766. 13625
  189767. DENMARK
  189768. CuALLYLATION CARBONYL TIN STEREOCHEM SYNCLINAL ANTIPERIPLANAR TRANSITION STATE ACID BRONSTED CYCLIZATION LEWIS STANNANEM
  189769. 14634N
  189770. 2/28/96
  189771. AESTEREOCHEMICAL STUDIES ON THE ADDITION OF ALLYLSTANNANES to ALDEHYDES
  189772. 1994X
  189773. 5133Y
  189774. 13626
  189775. COMMINS 
  189776. JOCC[ PYRIDINE LITHIATION SHORT EFFICIENT ALKALOID SYNTHESIS TARGET CAMPTOTHECIN CHIRAL COUPLINGM
  189777. 14635N
  189778. 2/28/96
  189779. A>A SIX STEP SYNTHESIS OF CAMPTOTHECIN USING PALLADIUM CHEMISTRY
  189780. 1994X
  189781. 5120Y
  189782. 13627
  189783. MATSUDA 
  189784. C}ALLYL SULFIDE SULFONE RADICAL SAMARIUM RING ANNULATION CARBOCYCLIC INTRODUCTION REDUCTIVE CYCLIZATION CARBONYL ADDITION VINYLM
  189785. 14636N
  189786. 2/28/96
  189787. AtSTEREOSELECTIVE CYCLIZATION MEDIATED BY SAMARIUM IODIDE USING ALLYL SULFIDES and SULFONES AS KETYL RADICAL ACCEPTORS
  189788. 1994X
  189789. 5111Y
  189790. 13628
  189791. JOCC?TANDEM ELIMINATION REDUCTION SULFONE CHIRAL REDUCTIVE REDUCTIONM
  189792. 14637N
  189793. 2/28/96
  189794. AxSTEREOSELECTIVE SYNTHESIS OF SUBSTITUTED CYCLOHEXANOLS FROM A FURANE DERIVED SULTONE VIA TANDEM ELIMINATION 1,6
  189795. ADDITION
  189796. 1994X
  189797. 3687Y
  189798. 13629
  189799. KOBAYESHI 
  189800. JOCCfLEWIS ACID AQUEOUS REACTION ACCELERATION RATE ENHANCEMENT ENOL SILYL ETHER LANTHANIDE EUROPIUM REAGENTM
  189801. 14638N
  189802. 2/28/96
  189803. A1LATHANIDE TRIFLATES AS WATER TOLERANT LEWIS ACIDS
  189804. 1994X
  189805. 3590Y
  189806. 13630
  189807. CURRAN
  189808. JOCCp LEWIS ACID RADICAL CYCLIZATION STEREOCHEM ADDITION ALLYLATION TIN SULFOXIDE COORDINATION COMPLEXATION MECHANISMM
  189809. 14640N
  189810. 2/28/96
  189811. AvALTERING THE STEREOCHEMISTRY OF ALLYLATION REACTIONS OF CYCLIC A-SULFINYL RADICALS EFFECTS OF SOLVENTS and LEWIS ACIDS
  189812. 1994X
  189813. 3547Y
  189814. 13632
  189815. HOFFMAN
  189816. JOCCVACYL IMINIUM ION REVIEW N
  189817. ACYL INTRODUCTION GENERATION ELIMINATION TRIFLUORO OXIDATIONM
  189818. 14641N
  189819. 2/28/96
  189820. A FACILE PREPARATION OF AMIDES BY GENERATION and TRAPPING OF N
  189821. ACYL IMINIUM IONS FROM IONIZATION REARRANGEMENT REACTIONS OF TRIFLYLOXY AMIDES
  189822. 1994X
  189823. 3530Y
  189824. 13633
  189825. MEYERS
  189826. Tet. Lett.CS OXIDATION OXAZOLE PREPARATION THIAZOLE NBS AMINO AMINE ESTER CHIRAL FUNCTIONALIZEDM
  189827. 14642N
  189828. 2/28/96
  189829. AbSTUDIES ON OXAZOLINE and THIAZOLINE OXIDATIONS.  A RELIABLE ROUTE to CHIRAL OXAZOLES and THIAZOLES
  189830. 1994X
  189831. 13634
  189832. CARRETERO 
  189833. Tet. Lett.CoDIHYDROFURAN ANION LITHIATE ADDITION VINYL CARBANION LACTONE CYCLIZATION CONJUGATE ADDITION SPIRO VINYL SULFONEM
  189834. 14643N
  189835. 2/28/96
  189836. A`ONE STEP FUNCTIONALIZATION OF DIOXASPIRODECANES FROM b-PHENYLSULFONYL DIHYDROFURANS and LACTONES
  189837. 1994X
  189838. 13635
  189839. DE GROOT
  189840. Tet. Lett.
  189841. CA ALLENE INTRAMOLECULAR ADDITION HETEROCYCLE HYDRAZINE CYCLIZATIONM
  189842. 14644N
  189843. 2/28/96
  189844. AANOVEL TANDEM CYCLIZATION
  189845. OXIDATION REACTION OF ALLENYL HYDRAZONES
  189846. 1994X
  189847. 13636
  189848. KURODA 
  189849. Tet. Lett.CDALLYL SILANE SPIRO MICHAEL ADDITION NAZAROV CYCLOPENTENONE CONJUGATEM
  189850. 14645N
  189851. 2/28/96
  189852. AQSYNTHESIS OF SPIRODECANE RING SYSTEM THROUGH ALLYLSILANE PROMOTED SPIROANNULATION
  189853. 1994X
  189854. 13637
  189855. GRIMM 
  189856. Tet. Lett.C]JULIA COUPLING INTRAMOLECULAR SULFONE TARGET REDUCTION CYCLIZATION SESQUITERPENE INTRODUCTIONM
  189857. 14646N
  189858. 2/28/96
  189859. ARTOTAL SYNTHESIS OF HELIANNUOL VIA INTRAMOLECULAR JULIA COUPLING REDUCTION SEQUENCE
  189860. 1994X
  189861. 13638
  189862. CAINE
  189863. Tet. Lett.CO FURANONE ANION CARBANION DISPLACEMENT HALIDE INTRAMOLECULAR CYCLIZATION TARGETM
  189864. 14647N
  189865. 2/28/96
  189866. ACSYNTHESIS OF OXABICYCLO UNDECENONE DERIVATIVES FROM 3(2H)
  189867. FURANONES
  189868. 1994X
  189869. 13639
  189870. GRIECO
  189871. Tet. Lett.Cz CATALYST LITHIUM PERCHLO           RATE INTRAMOLECULAR DIENE ISOMERIZATION ACID LEWIS DIELS
  189872. ALDER ETHER 4+2 REARRANGEMENTM
  189873. 14648N
  189874. 2/28/96
  189875. A{ACID CATALYZED INTRAMOLECULAR DIELS
  189876. ALDER REACTIONS IN LITHIUM PERCHLORATE
  189877. DIETHYL ETHER.  ACID PROMOTED MIGRATION OF DIENE
  189878. 1994X
  189879. 13640
  189880. KANEMATSU 
  189881. J.C.S. Chem. Commun.Ck ALLENE FURAN INTRAMOLECULAR ALKYNE ISOMERIZATION PROPARGYL ETHER SESQUITERPENE TARGET DIELS
  189882. ALDER TRANSFERM
  189883. 14649N
  189884. 2/28/96
  189885. A`TOTAL SYNTHESIS OF LACTONE SESQUITERPENES USING INTRAMOLECULAR DIELS ALDER REACTION OF AN ALLENE
  189886. 1994X
  189887. 13641
  189888. RAVINDRANATHAN 
  189889. J.C.S. Chem. Commun.CZPROTECTION KETONE DEPROTECTION KETAL OXATHIA ACYL ANION EQUIVALENT HYDROLYSIS EXPERIMENTALM
  189890. 14650N
  189891. 2/28/96
  189892. VvUNUSUALLY FACILE OXATHIOACETAL TRANSFER REACTION.  AN EFFICIENT HIGHLY STEREOSELECTIVE CATALYTIC DEPROTECTION PROTOCOLW
  189893. 1994X
  189894. 13642
  189895. GILLMAN 
  189896. SynlettCOALLENE ESTER HALIDE CROSS
  189897. COUPLING PALLADIUM BORON SUZUKI ADDITIVE SILVER OXIDEM
  189898. 14651N
  189899. 2/28/96
  189900. AjSILVER OXIDE ASSISTED PALLADIUM CATALYZED CROSS COUPLING OF HALO 2,3
  189901. BUTADIENOATES WITH ARYL BORONIC ACIDS
  189902. 1994X
  189903. 13643
  189904. OSHIMA 
  189905. SynlettCbLITHIUM HALOGEN EXCHANGE ALKENYL BUTYL LITHIUM BULI ELECTROPHILE ALKENE RETENTION STEREOCHEM VINYLM
  189906. 14652N
  189907. 2/28/96
  189908. A ROOM TEMPERATURE PREPARATION OF ALKENYLLITHIUMS BY LITHIUM
  189909. HALOGEN EXCHANGE BETWEEN ALKENYL IODIDES and N
  189910. BU LITHIUM IN HYDROCARBON SOLVENTS
  189911. 1994X
  189912. 13644
  189913. SAKAMOTO
  189914. SynlettCo NITRONE CHIRAL ASYMMETRIC DIPOLAR
  189915. CYCLOADDITION DIASTEREOSELECTIVE TRANSITION STATE STERIC INTERACTION KINETICM
  189916. 14653N
  189917. 2/28/96
  189918. TANDEM TRANSESTERIFICATION and DIASTEREOSELECTIVE INTRAMOLECULAR CYCLOADDITION OF METHOXY CARBONYL NITRONES WITH CHIRAL ACYCLIC ALLYL ALCOHOLS
  189919. 1994X
  189920. 13645
  189921. ISOBE
  189922. SynlettCP TRIFLATE PYRIDINE COUPLING CROSS ARYL SILYL ALKYNYL STILLE NITROGEN HETEROCYCLEM
  189923. 14654N
  189924. 2/28/96
  189925. AzINTRODUCTION OF AN ACETYLENE MOIETY INTO AMIDE CARBONS VIA PALLADIUM COUPLING and ITS APPLICATION FOR A MODEL OF DYNEMICIN
  189926. 1994X
  189927. 13646
  189928. JULIA
  189929. J.C.S. Chem. Commun.Co ALLYL SULFONE EQUIVALENT ANION SULFONYL INTRODUCTION REDUCTION ELECTROPHILIC ADDITION ALDEHYDE DESULFONYLATIONM
  189930. 14655N
  189931. 2/28/96
  189932. ALLYLIC SULFONES AS ALLYL ANION EQUIVALENTS HOMOALLYLIC ALCOHOLS FROM METAL CATALYZED REACTIONS OF SULFONES WITH ALDEHYDES and KETONES
  189933. 1994X
  189934. 13647
  189935. A    BRAVERMAN
  189936. Tet. Lett.C
  189937.  ALLENE SULFONE CHLORO TRICHLORO ACTIVATED RATE FACILE DIELS
  189938. ALDER SUPER REACTIVITY INCREASED STEREOSELECTIVITY ALLENYL CYCLOADDITIONM
  189939. 14656N
  189940. 2/28/96
  189941. AjFACILE, REGIO and STEREOSELECTIVE DIELS
  189942. ALDER REACTIONS OF ALLENIC TRICHLOROMETHYL SULFONES and SULFOXIDES
  189943. 1994X
  189944. 13648
  189945. HERRERA
  189946. Tet. Lett.CK RHODIUM DIAZO KETO ESTER ACETATE ACETOXY REARRANGEMENT 1,2 SHIFT CARBENOIDM
  189947. 14657N
  189948. 2/28/96
  189949. AWOXY DIAZO CARBONYL COMPOUNDS RHODIUM(II) MEDIATED DECOMPOSITION OF ACETOXY DIAZO ESTERS
  189950. 1994X
  189951. 13649
  189952. OTERA 
  189953. Tet. Lett.CBSIGMATROPIC 2,3 REARRANGEMENT ALLYLIC SULFOXIDE STEREOCHEM ALCOHOLM
  189954. 14658N
  189955. 2/28/96
  189956. A?HYDROXYL DIRECTED STEREOSELECTIVE 2,3
  189957. SIGMATROPIC REARRANGEMENT
  189958. 1994X
  189959. 13650
  189960. UENISHI 
  189961. Tet. Lett.C:EPISULFIDE ELIMINATION ALKENE BORON DESULFURIZATION CHIRALM
  189962. 14659N
  189963. 2/28/96
  189964. A.AN EXTREMELY MILD DESULFURIZATION OF THIIRANES
  189965. 1994X
  189966. 13651
  189967. LANGE
  189968. Tet. Lett.CF RADICAL CYCLIZATION 2+2 ADDUCT IODO RING OPENING RADICAL TIN SAMARIUMM
  189969. 14660N
  189970. 2/28/96
  189971. FREE RADICAL FRAGMENTATION OF PHOTOADDUCT DERIVATIVES to ALLYLIC SYSTEMS.  REGIOSELECTIVITY OF REDUCTION WITH TIN HYDRIDES and SAMARIUM IODIDE
  189972. 1994X
  189973. 13652
  189974. Tet. Lett.CiNITRO TOLUENE FLUORIDE UNSATURATED MICHAEL DISPLACEMENT IPSO MECHANISM NUCLEOPHILIC AROMATIC SUBSTITUTIONM
  189975. 14661N
  189976. 2/28/96
  189977. AQFLUORIDE CATALYZED INTRAMOLECULAR DENITRO CYCLIZATION OF NITROTOLUENES to INDANES
  189978. 1994X
  189979. 13653
  189980. WEST 
  189981. JACSC
  189982. AMINO AMINE DIAZO CHIRAL KETONE RHODIUM CARBENOID AMMONIUM YLIDE REARRANGEMENT 1,2 SHIFT STEREOCHEM ENANTIOSELECTIVE DIASTEREOSELECTIVE ALKALOIDM
  189983. 14662N
  189984. 2/28/96
  189985. AYPIPERIDINES VIA AMMONIUM YLIDE 1,2
  189986. SHIFTS.  A CONCISE ENANTIOSELECTIVE ROUTE to ALKALOIDS
  189987. 1994X
  189988. 8420Y
  189989. 13654
  189990. HERGES
  189991. JACSCS DIAZO CARBENE ALKYNE REARRANGEMENT PROPARGYLENE CYCLOPROPANATION THEORY SCRAMBLINGM
  189992. 14663N
  189993. 2/28/96V
  189994. PROPARGYLENEW
  189995. 1994X
  189996. 8229Y
  189997. 13655
  189998. PLATZ 
  189999. JACSC2DIAZO SYN ANTI WOLFF KETENE LASER FLASH PHOTOLYSISM
  190000. 14664N
  190001. 2/28/96V4CARBOETHOXY CARBENE.  A LASER FLASH PHOTOLYSIS STUDYW
  190002. 1994X
  190003.  8146Y
  190004. 13656
  190005. WARKENTIN 
  190006. EXTRUSION NITROGEN CARBONYL YLIDE CLEAVAGE DIALKOXY CARBENE ADDITION ALKYNE INTRAMOLECULAR STRAINED CYCLOPROPENE INSERTION 2+2 CYCLOBUTANE NOVEL OXADIAZOLINEM
  190007. 14665N
  190008. 2/28/96
  190009. A\THERMOLYSIS OF OXADIAZOLINE IN SOLUTION.  A REMARKABLE CASCADE OF CARBENE and OTHER REACTION
  190010. 1994X
  190011. 5071Y
  190012. 13657
  190013. GOTI 
  190014. Tet. Lett.COHYDROXYL AMINE OXIDATION REAGENT NITRONE LEY PERRUTHENATE DIPOLAR
  190015. CYCLOADDITIONM
  190016. 14666N
  190017. 2/28/96
  190018. HIGHLY EFFICIENT and MILD SYNTHESIS OF NITRONES BY CATALYTIC OXIDATION OF HYDROXYLAMINES WITH TETRA
  190019. PROPYLAMMONIUM PERRUTHENATE
  190020. 1994X
  190021. 13658
  190022. GOTI 
  190023. Tet. Lett.CYOXIDATION AMINE IMINE REAGENT PERRUTHENATE LEY OXIDANT ALCOHOL ALDEHYDE MILD EXPERIMENTALM
  190024. 14667N
  190025. 2/28/96
  190026. APCATALYTIC OXIDATION OF SECONDARY AMINES WITH TETRA
  190027. PROPYLAMMONIUM PERRUTHENATE
  190028. 1994X
  190029. 13659
  190030. WELLS
  190031. Tet. Lett.CH NITRILE OXIDE DIPOLAR
  190032. CYCLOADDITION REGIOCHEM NMR STRUCTURE ISOXAZOLINEM
  190033. 14668N
  190034. 2/28/96
  190035. AXCONTROL OF REGIOSELECTIVITY IN NITRILE OXIDE CYCLOADDITIONS to CINNAMIC ACID DERIVATIVES
  190036. 1994X
  190037. 13660
  190038. ANGLE 
  190039. Tet. Lett.ClALLYL SILANE SILICON BENZYLIC CATION MIGRATION SILYL CYCLOPENTANE DIPOLE EQUIVALENT LEWIS
  190040. ACID DIHYDROINDENEM
  190041. 14669N
  190042. 2/28/96
  190043. AHFORMAL 3+3 and 3+2 CYCLOADDITIONS OF ALLYL SILANES WITH BENZYLIC CATIONS
  190044. 1994X
  190045. 13661
  190046. WASSERMAN 
  190047. JOCCRWITTIG CYANO PHOSPHOROUS DICARBONYL ACID CHLORIDE KETO ACID AMIDE OZONE OZONOLYSISM
  190048. 14670N
  190049. 2/28/96
  190050. A}CYANOMETHYLENE PHOSPHORANES AS NOVEL CARBONYL 1,1
  190051. DIPOLE SYNTHONS.  AN EFFICIENT SYNTHESIS OF A-KETO ACIDS, ESTERS and AMIDES
  190052. 1994X
  190053. 4364Y
  190054. 13662
  190055. SAITO
  190056. JOCCp PHENOL PHENOXIDE ADDITION ANION ALKYNE BALDWIN INTRAMOLECULAR ACETYLENE DIGONAL 5
  190057. EXO 6
  190058. ENDO REVERSIBLE WRITINGM
  190059. 14671N
  190060. 2/28/96
  190061. HIGHLY EFFICIENT SYNTHESIS OF 2
  190062. SUBSTITUTED 4H
  190063. CHROMEN
  190064. ONES BY MEANS OF FLUORIDE INDUCED 6
  190065. ENDO DIGONAL CYCLIZATION OF AN ALKYNYL KETONE
  190066. 1994X
  190067. 4360Y
  190068. 13663
  190069. DAVIES
  190070. JOCC`VINYL CARBENOID DIAZO RHODIUM MECHANISM STEPWISE TERMINUS SOLVENT COMPETITION WRITING ZWITTERIONM
  190071. 14672N
  190072. 2/28/96
  190073. AMCARBENOID VERSUS VINYLOGOUS REACTIVITY IN RHODIUM STABILIZED VINYL CARBENOIDS
  190074. 1994X
  190075. 4535Y
  190076. 13664
  190077. MIDLAND 
  190078. JOCCQCONFORMATIONAL MOLECULAR MODELING MM2 COUPLING CONSTANT WRITING NMR BAKMDL GLOBALM
  190079. 14673N
  190080. 2/28/96
  190081. ATSYNTHESIS and CONFORMATIONAL ANALYSIS OF SUGARS.  NMR and MOLECULAR MODELING STUDIES
  190082. 1994X
  190083. 4438Y
  190084. 13665
  190085. SAITO
  190086. JOCCfALKYNE ALKOXIDE ADDITION ENDO EXO DIGONAL INTRAMOLECULAR STEREOCHEM STUDENT KRUMPE FLUORIDE CHROMENONEM
  190087. 14674N
  190088. 2/28/96
  190089. HIGHLY EFFICIENT SYNTHESIS OF 2
  190090. SUBSTITUTED 4H
  190091. CHROMEN
  190092. ONES BY MEANS OF A FLUORIDE INDUCED 6
  190093. ENDO DIGONAL CYCLIZATION OF A ETHYNYL KETONE DERIVATIVE
  190094. 1994X
  190095. 4360Y
  190096. 13666
  190097. WAGNER 
  190098. JACSCT2+2 BENZENE ALKENE PHOTOCHEMISTRY INTRAMOLECULAR DIRADICAL CYCLOPROPYL RADICAL CLOCKM
  190099. 14675N
  190100. 2/28/96
  190101. A_BIRADICAL REARRANGEMENT DURING INTRAMOLECULAR CYCLOADDITION OF DOUBLE BONDS to TRIPLET BENZENES
  190102. 1994X
  190103. 7945Y
  190104. 13667
  190105. HARMAN 
  190106. JACSC]PYRROLE OSMIUM COMPLEX CYCLOADDITION INDOLE COURSE ALKALOID INTRODUCTION METAL ORGANOMETALLICM
  190107. 14676N
  190108. 2/28/96
  190109. AZAFULVENIUM and 3
  190110. VINYL PYRROLE COMPLEX OF OSMIUM FROM A h-PYRROLE and ITS EFFICIENT CONVERSION INTO A HIGHLY SUBSTITUTED INDOLE
  190111. 1994X
  190112. 7931Y
  190113. 13668
  190114. A    BUCHWALD 
  190115. JACSCXPALLADIUM CATALYSIS AROMATIC ARYL HALIDE AMINE AMINATION TIN STANNANE TRANSIENT COUPLINGM
  190116. 14677N
  190117. 2/28/96
  190118. AMPALLADIUM CATALYZED AROMATIC AMINATION WITH IN SITU GENERATED AMINO STANNANES
  190119. 1994X
  190120. 7901Y
  190121. 13669
  190122. KLARNER 
  190123. JACSCVDIELS
  190124. ALDER PRESSURE VOLUME INTRODUCTION ACTIVATION TRANSITION STATE CYCLOADDITION 4+2M
  190125. 14678N
  190126. 2/28/96
  190127. EVIDENCE FOR PERICYCLIC and STEPWISE PROCESSES IN THE CYCLODIMERIZATION OF CHLOROPRENE AND BUTADIENE FROM PRESSURE DEPENDENCE and STEREOCHEMISTRY
  190128. 1994X
  190129. 7646Y
  190130. 13670
  190131. A    SZEIMIES 
  190132. JACSCYCARBENE INSERTION BRIDGEHEAD REARRANGEMENT BICYCLIC EATON JONES TRAPPING CYCLOPROPANATIONM
  190133. 14679N
  190134. 2/28/96
  190135. REACTION OF 1
  190136. HALOMETHYL BICYCLO[1.1.1]PENTANE WITH STRONG BASES.  EVIDENCE FOR A CARBENE BRIDGEHEAD OLEFIN
  190137. CARBENE REARRANGEMENT
  190138. 1994X
  190139. 7637Y
  190140. 13671
  190141. WULFF
  190142. JACSCsFISCHER CARBENE COMPLEX WRITING ANNULATION INTRODUCTION CHROMIUM PHENOL ALKYNE DIYNE CYCLIZATION MECHANISM TUNGSTENM
  190143. 14680N
  190144. 2/28/96
  190145. AyTHREE COMPONENT INTRAMOLECULAR TWO ALKYNE ANNULATIONS OF FISCHER CARBENE COMPLEXES.  NEW STRATEGIES FOR STEROID SYNTHESIS
  190146. 1994X
  190147. 7616Y
  190148. 13672
  190149. IWATA 
  190150. J.C.S. Chem. Commun.CkCYCLOPROPYL SULFIDE CERIC RADICAL CATION RING OPENING DICATION CYCLIZATION ALCOHOL TETHERED TETRAHYDROFURANM
  190151. 14681N
  190152. 2/28/96
  190153. ApTANDEM OXIDATIVE RING CLEAVAGE
  190154. CYCLIZATION REACTIONS OF CYCLOPROPYLSULFIDES.  A NOVEL SYNTHESIS OF CYCLIC ETHERS
  190155. 1994X
  190156. 13673
  190157. SCHINZER
  190158. Synlett
  190159. CKTANDEM HETEROCYCLE BECKMANN ALLYL SILANE CYCLIZATION CEPHALOTAXINE SKELETONM
  190160. 14682N
  190161. 2/28/96
  190162. BECKMANN REARRANGEMENT ALLYLSILANE CYCLIZATIONS APPROACH to THE PENTACYCLIC CEPHALOTAXINE FRAMEWORK and THE INFLUENCE OF THE TERMINATING SILICON GROUP
  190163. 1994 X
  190164. 13674
  190165. A    MALACRIA 
  190166. SynlettClASYMMETRIC RADICAL CYCLIZATION VINYL SULFOXIDE TETRAHYDROFURAN DIASTEREOSELECTIVITY TRANSITION STATE WRITINGM
  190167. 14683N
  190168. 2/28/96
  190169. AtGOOD to EXCELLENT DIASTEREOSELECTIVITIES IN ASYMMETRIC RADICAL CYCLIZATION OF OPTICALLY PURE ALKOXY VINYL SULFOXIDES
  190170. 1994X
  190171. 13675
  190172. IKEGAMI 
  190173. SynlettCcRHODIUM DIAZO CARBENOID INSERTION STEREOCHEM ENANTIOSELECTIVITY CATALYST LIGAND SUBSTITUENT WRITINGM
  190174. 14684N
  190175. 2/28/96
  190176. ENANTIOSELECTIVE INTRAMOLECULAR C
  190177. H INSERTION REACTION OF DIAZO KETOESTERS CATALYZED BY RHODIUM(II) CARBOXYLATES.  THE EFFECT OF THE SUBSTITUENT AT THE INSERTION SITE ON ENANTIOSELECTIVITY
  190178. 1994X
  190179. 13676
  190180. NAKAI 
  190181. SynlettC>AZABICYCLIC POISON FROG OPIOD MORPHINE INTRODUCTION BANKS ARMY
  190182. 14685N
  190183. 2/28/96
  190184. A@SYNTHESIS and BIOLOGICAL EVALUATION OF EPIBATIDINE and CONGENERS
  190185. 1994X
  190186. 13677
  190187. DE MESMAAKER 
  190188. SynlettCUSELENIDE RADICAL SUGAR TIN CYCLIZATION EPIMERIZATION OXYALLYL ADDITION INTRAMOLECULARM
  190189. 14686N
  190190. 2/28/96
  190191. EPIMERIZATION IN GLYCOPYRANOSIDES DURING THE CYCLIZATION OF ANOMERIC RADICALS.  EASE OF THE INTRAMOLECULAR 1,5
  190192. HYDROGEN ATOM TRANSFER
  190193. 1994X
  190194. 13678
  190195. JACSM
  190196. 14687N
  190197. 2/28/96
  190198. AHCARBENE
  190199. CARBENE INTERCONVERSION BETWEEN 1- and 3
  190200. PHENYL
  190201. PROPYNYLIDENES
  190202. 1994X
  190203. 6179Y
  190204. 13679
  190205. AGGARWAL
  190206. JACSCMSULFUR YLIDE RHODIUM DIAZO ESTER ALDEHYDE EPOXIDE PREPARATION CATALYTIC CYCLEM
  190207. 14688N
  190208. 2/28/96
  190209. NOVEL CATALYTIC CYCLE FOR THE SYNTHESIS OF EPOXIDES FROM ALDEHYDES and SULFUR YLIDES MEDIATED BY CATALYTIC QUANTITIES OF SULFIDES and RHODIUM(II) ACETATE
  190210. 1994X
  190211. 5973Y
  190212. 13680
  190213. BOYER 
  190214. JOCCdCYCLOPROPENONE KETALS DIELS
  190215. ALDER CYCLOPROPENE TARGET TROPOLONE ANNULATION NATURAL PRODUCT SYNTHESISM
  190216. 14689N
  190217. 2/28/96
  190218. AkDIELS
  190219. ALDER REACTIONS OF CYCLOPROPENONE KETALS.  A CONCISE TROPOLONE ANNULATION APPROACH to TOTAL SYNTHESIS
  190220. 1994X
  190221. 3453Y
  190222. 13681
  190223. JOCCdPHENOL THIOPHENYL PUMMERER REARRANGEMENT SULFOXONIUM KETO WRITING NUCLEOPHILIC BIARYL COUPLING NOVELM
  190224. 14690N
  190225. 2/28/96
  190226. VARIOUS NUCLEOPHILIC AROMATIC SUBSTITUTION VIA TRAPPING OF AN A-KETOSULFONIUM ION GENERATED BY PUMMERER TYPE REARRANGEMENT.  PREPARATION OF BIARYLS
  190227. 1994X
  190228. 3248Y
  190229. 13682
  190230. SEMMELHACK
  190231. JOCCL DIYNE BERGMAN DIRADICAL ENE WRITING REARRANGEMENT TRIGGERING RATE HALF LIVEM
  190232. 14691N
  190233. 2/28/96
  190234. A5ARENE 1,4
  190235. DIRADICAL FORMATION FROM O
  190236. DIALKYNYL ARENES
  190237. 1994X
  190238. 5038Y
  190239. 13683
  190240. HEGEDUS 
  190241. JOCCmPHOTOCHEMICAL CHROMIUM CARBENE COMPLEX STEREOCHEM TORQUOSELECTIVITY STAUDINGER THEORY CALCULATIONS 2+2 LACTAMM
  190242. 14692N
  190243. 2/28/96
  190244. ELECTRONIC EFFECTS ON THE STEREOCHEMICAL OUTCOME OF THE PHOTOCHEMICAL REACTION OF CARBENE COMPLEXES WITH IMINES to FORM b-LACTAMS
  190245. 1994X
  190246. 4967Y
  190247. 13684
  190248. FARINA
  190249. JOCCeCEPHALOSPORIN ALLENE CUPRATE ADDITION DISPLACEMENT DISULFIDE CYCLIZATION CLOSURE SULFONE DISPLACEMENTM
  190250. 14693N
  190251. 2/28/96
  190252. A NOVEL APPROACH to CEPHALOSPORINS FROM ALLENYL AZETIDINONES.  A NEW CYCLIZATION STRATEGY VIA TANDEM CUPRATE ADDITION SULFENYLATION
  190253. 1994X
  190254. 4956Y
  190255. 13685
  190256. BOYER 
  190257. JOCCfTRIAZINE AMIDINE DIELS
  190258. ALDER HETEROCYCLE 4+2 EXTRUSION INVERSE ELECTRON DEMAND AZADIENE HETEROAROMATICM
  190259. 14694N
  190260. 2/28/96
  190261. INVERSE ELECTRON DEMAND DIELS
  190262. ALDER REACTIONS OF HETEROCYCLIC AZADIENES.  4+2
  190263. CYCLOADDITION REACTION OF AMIDINES WITH TRIAZINES
  190264. 1994X
  190265. 4950Y
  190266. 13686
  190267. DANHEISER 
  190268. JOCCx2+2 WOLFF DIAZO TARGET HYDROQUINONE SYNTHESIS KETENE ALKOXY ALKYNE RING OPENING KETENE CYCLIZATION ELECTROCYCLIC QUINONEM
  190269. 14695N
  190270. 2/28/96
  190271. A?USE OF DIAZO KETONE 
  190272.  ALKOXY ALKYNE REACTION IN TOTAL SYNTHESIS
  190273. 1994X
  190274. 4844Y
  190275. 13687
  190276. FALVEY
  190277. JOCCE RADICAL CLOCK BIOORGANIC DNA INTRODUCTION WRITING RATE REARRANGEMENTM
  190278. 14696N
  190279. 2/28/96
  190280. A0FREE RADICAL REARRANGEMENT IN URACIL DERIVATIVES
  190281. 1994X
  190282. 4791Y
  190283. 13688
  190284. MORDINI 
  190285. JOCC>EPOXIDE ALCOHOL RING OPENING ALKOXY STEREOCHEM ALLYLIC ALCOHOLM
  190286. 14697N
  190287. 2/28/96
  190288. ARHETEROATOM ASSISTED ISOMERIZATION OF EPOXIDES to ALLYLIC ALCOHOLS PROMOTED BY BASE
  190289. 1994X
  190290. 4784Y
  190291. 13689
  190292. NEGISHI
  190293. JOCC[PALLADIUM ARYL HALIDE ALLENE INTRAMOLECULAR ALKOXY CYCLIZATION CYCLOALKENE CARBOPALLADATIONM
  190294. 14698N
  190295. 2/28/96
  190296. AnFACILE FORMATION OF SEVEN and EIGHT MEMBERED CYCLOALKENES VIA CATALYTIC and CYCLIC CARBOPALLADATION OF ALLENES
  190297. 1994X
  190298. 4730Y
  190299. 13690
  190300. IWATA 
  190301. CmRADICAL CATION CYCLOPROPANE CYCLOPROPYL THIO RING OPENING CYCLIZATION NUCLEOPHILE OXIDATIVE CHIRAL ASYMMETRICM
  190302. 14699N
  190303. 2/28/96
  190304. CHIRALITY PRESERVATION OF A CATION RADICAL INTERMEDIATE.  TANDEM OXIDATIVE RING EXPANSION 
  190305.  CYCLIZATION REACTION OF BICYCLO[4.1.0]HEPTYL SULFIDES
  190306. 1994X
  190307. 4727Y
  190308. 13691
  190309. YAMAMOTO
  190310. JOCCMDIAZO KETONE CARBONYL LEWIS ACID RING EXPANSION ALUMINUM HOMOLOGATION EPOXIDEM
  190311. 14700N
  190312. 2/28/96
  190313. AAORGANOALUMINUM PROMOTED HOMOLOGATION OF KETONES WITH DIAZOALKANES
  190314. 1994X
  190315. 4725Y
  190316. 13692
  190317. CLARK 
  190318. Tet. Lett.
  190319. C^RHODIUM DIAZO ETHER CARBENOID CARBONYL YLIDE OXONIUM REARRANGEMENT TANDEM TARGET WRITING SHIFTM
  190320. 14701N
  190321. 2/28/96
  190322. AmA SHORT SYNTHESIS OF A TARGET BY A TANDEM INTRAMOLECULAR CARBENOID INSERTION and YLIDE REARRANGEMENT REACTION
  190323. 1994X
  190324. 13693
  190325. BOWMAN 
  190326. Tet. Lett.C`SELENIUM RADICAL TIN IMINE HYDRAZONE CYCLIZATION NITROGEN AMINE INTRAMOLECULAR AMINO HETEROCYCLEM
  190327. 14702N
  190328. 2/28/96
  190329. A;CYCLIZATION OF CARBINYL RADICALS ONTO IMINES and HYDRAZONES
  190330. 1994X
  190331. 13694
  190332. RESNATI 
  190333. Tet. Lett.CUOXAZIRIDINE PERFLUORO OXIDATION SILANE SILANOL ENANTIOSELECTIVE HYDROXYLATION SILICONM
  190334. 14703N
  190335. 2/28/96
  190336. A~OXYFUNCTIONALIZATION REACTIONS OF PERFLUORO CIS 2,3
  190337. DIALKYLOXAZIRIDINES.  ENANTIOSELECTIVE CONVERSION OF SILANES INTO SILANOLS
  190338. 1994X
  190339. 13695
  190340. CAHIEZ
  190341. Tet. Lett.CMSILYL ENOL ETHER STEREOCHEM MANGANESE STEREOSPECIFIC SILICON Z E STEREOISOMERM
  190342. 14704N
  190343. 2/28/96
  190344. ArHIGHLY REGIO and STEREOSELECTIVE PREPARATION OF Z SILYL ENOL ETHERS and ESTERS FROM KETONES VIA MANGANESE ENOLATES
  190345. 1994X
  190346. 13696
  190347. CURRAN
  190348. Tet. Lett.CRRADICAL TRANSFER CHIRAL ASYMMETRIC SELENIUM GROUP FELKIN
  190349. ANY CRAM TRANSITION STATEM
  190350. 14705N
  190351. 2/28/96
  190352. GROUP TRANSFER ADDITION REACTIONS OF SELENOMALONITRILES to CHIRAL ENOL ETHERS.  ASYMMETRIC RADICAL ADDITION and SELENIUM TRANSFER REACTIONS
  190353. 1994X
  190354. 13697
  190355. PIRRUNG 
  190356. Tet. Lett.CgDIAZO CARBONYL RHODIUM CARBENOID VINYL ESTER CYCLOPROPANATION ELIMINATION FURAN TARGET CYCLOHEXANEDIONEM
  190357. 14706N
  190358. 2/28/96
  190359. A=DIPOLAR CYCLOADDITION OF RHODIUM CARBENOIDS WITH VINYL ESTERS
  190360. 1994X
  190361. 13698
  190362. PIRRUNG 
  190363. Tet. Lett.C{DIAZO CARBONYL RHODIUM CARBENOID CYCLOHEXANEDIONE ALKYNE FURAN CYCLOPROPENE WRITING VINYL CARBENE ELECTROCYCLIZATION TARGETM
  190364. 14707N
  190365. 2/28/96
  190366. A]DIPOLAR CYCLOADDITION OF CYCLIC RHODIUM CARBENOIDS to DOGONAL CARBON. SYNTHESis OF ISOEPURINE
  190367. 1994X
  190368. 13699
  190369. COLLUM 
  190370. Tet. Lett.CQSODIUM BOROHYDRIDE REDUCTION REDUCING AGENT AQUEOUS TIN RADICAL CYCLIZATION NABH4M
  190371. 14708N
  190372. 2/28/96
  190373. A`REDUCTIONS and RADICAL CYCLIZATIONS OF ARYL and ALKYL BROMIDES MEDIATED BY NABH4 IN AQUEOUS BASE
  190374. 1994X
  190375. 13700
  190376. COSSY 
  190377. Tet. Lett.CeCYCLOALKANE DIONE BETA KETO ESTER CYCLOPENTENONE OXIDATIVE CLEAVAGE KETO 1,2
  190378. DIKETONE CARBOXYLIC ACIDM
  190379. 14709N
  190380. 2/28/96
  190381. AsOXIDATIVE CLEAVAGE OF 2
  190382. SUBSTITUTED CYCLOALKANE 1,3
  190383. DIONES and OF CYCLIC b-KETO ESTERS BY COPPER PERCHLORATE/OXYGEN
  190384. 1994X
  190385. 13701
  190386. LINDERMAN 
  190387. Tet. Lett.CJTIN STANNANE ETHER CLEAVAGE OZONE OXIDATION CARBONYL KETONE REGIOSELECTIVEM
  190388. 14710N
  190389. 2/28/96
  190390. A^REGIOSELECTIVE OXIDATIVE CLEAVAGE OF FUNCTIONALIZED UNSYMMETRIC TETRAALKYL STANNANES VIA OZONE
  190391. 1994X
  190392. 13702
  190393. LAUTOS 
  190394. Tet. Lett.CMSIGMATROPIC AMINO KETONE OXIME 3,3
  190395.  NITRONE REARRANGEMENT COPE HETERO IMIDATEM
  190396. 14711N
  190397. 2/28/96
  190398. ATSYNTHESIS OF A-AMIDO KETONES.  AN APPLICATION OF THE MULTI HETERO COPE REARRANGEMENT
  190399. 1994X
  190400. 13703
  190401. COREY, E. J.
  190402. JACSCZALDEHYDE, ACETYLENE, CARBONYL ADDITION OF ACETYLIDE, OPTICALLY ENRICHED PROPARGYL ALCOHOLSM
  190403. 14712
  190404. 2/28/96
  190405. AUHIGHLY ENANTIOSELECTIVE ALKYNYLATION OF ALDEHYDES PROMOTED BY CHIRAL OXAZABOROLIDINES
  190406. 1994X    3151
  190407. 3152Y
  190408. 13704
  190409. OPPOLZER
  190410. JACSC2HYDROXYLAMINE, RETRO
  190411. COPE ELIMINATION, PYRROLIDINEM
  190412. 14713N
  190413. 2/28/96
  190414. AlSUPRAFACIALITY OF THERMAL N
  190415. ALKENYLHYDROXYLAMINE CYCLIZATIONS:  SYNTHESES OF A-LYCORANE and (+)
  190416. TRIANTHINE
  190417. 1994X    3139
  190418. 3140Y
  190419. 13705
  190420. CURRAN
  190421. JACSCPHINDERED ROTATION, RADICAL, DIPOLAR CYCLOADDITIONS, NITRILE OXIDES, IMIDE, AMIDEM
  190422. 14714N
  190423. 2/28/96
  190424. AEATROPSELECTIVE THERMAL REACTIONS OF AXIALLY TWISTED AMIDES and IMIDES
  190425. 1994X    3131
  190426. 3132Y
  190427. 13706
  190428. FUKUYAMA
  190429. JACSCyORTHO ALKENYL ARYL ISONITRILE, TIN HYDRIDE, ALPHA STANNYLIMIDOYL RADICAL, IMIDOYL, CYCLIZATION TO INDOLE, STILLE COUPLINGM
  190430. 14715N
  190431. 2/28/96
  190432. A%A NOVEL TIN
  190433. MEDIATED INDOLE SYNTHESIS
  190434. 1994X    3127
  190435. 3128Y
  190436. 13707
  190437. HOVEYDA
  190438. JACSCjCARBOMAGNESIATION, KINETIC RESOLUTION, DIHYDROPYRAN, GRUBBS' METATHESIS OF DIENE, CHIRAL ZIRCONIUM COMPLEXM
  190439. 14716N
  190440. 2/28/96
  190441. A1ZIRCONIUM
  190442. CATALYZED KINETIC RESOLUTIONS OF PYRANS
  190443. 13708
  190444. MIKAMI
  190445. JACSCEDIENE, JUGLONE, QUINONE, METHYL GLYOXYLATE, CYCLOHEXENE, DIHYDROPYRANM
  190446. 14717N
  190447. 2/28/96
  190448. ASASYMMETRIC CATALYSIS OF DIELS
  190449. ALDER CYCLOADDITIONS WITH BINAPHTHOL
  190450. TITANIUM COMPLEX
  190451. 1994X    2812
  190452. 2820Y
  190453. 13709
  190454. EVANS
  190455. JACSCDALKENE, AZIRIDINE, NITRENE, ENOL SILANE, ALPHA AMINO KETONE, RACEMICM
  190456. 14718N
  190457. 2/28/96
  190458. AADEVELOPMENT OF THE COPPER
  190459. CATALYZED OLEFIN AZIRIDINATION REACTION
  190460. 1994X    2742
  190461. 2753Y
  190462. 13710
  190463. DEKIMPE
  190464. Tet. Lett.CRIMINE, ALKENE, BROMINE, IMINIUM SALT, REDUCTION WITH LAH, AZIRIDINIUM INTERMEDIATEM
  190465. 14719N
  190466. 2/28/96
  190467. AjELECTROPHILE
  190468. INDUCED CYCLIZATION OF g,d-ALKENYLIMINES AS A SYNTHETIC ROUTE to PYRROLIDINES and PIPERIDINES
  190469. 1994X
  190470. 13711
  190471. BLERIOT
  190472. TELLIER
  190473. Tet. Lett.CFGANEM
  190474. TYPE AMIDINES, SWAINSONINE, MORE POTENT THAN DEOXYMANNOJIRIMYCINM
  190475. 14720N
  190476. 2/28/96
  190477. ATSYNTHESIS OF A BENZYLAMIDINE DERIVED FROM D
  190478. MANNOSE.  A POTENT MANNOSIDASE INHIBITOR
  190479. 1994X    1867
  190480. 1870Y
  190481. 13712
  190482. Tet. Lett.C
  190483. ALDEHYDE MAY BE TREATED WITH A VARIETY OF LEWIS
  190484. ACID PROMOTED C
  190485. C BOND FORMATION REAGENTS WITHOUT HARMING OZONIDE, WHICH MAY BE CONVERTED TO ALDEHYDE WITH PH3P OR TO ACID WITH NAOHM
  190486. 14721N
  190487. 2/28/96
  190488. AAOZONIDES AS ALDEHYDE PROTECTING GROUPS and ACID PROTECTING GROUPS
  190489. 1994X    1743
  190490. 1746Y
  190491. 13713
  190492. ZARD 
  190493. Tet. Lett.CHAMIDE ALPHA RADICALS, ATOM TRANSFER CYCLIZATION, ADDITION TO PHENYL RING
  190494. 14722N
  190495. 2/28/96
  190496. ARRADICAL BASED SYNTHESIS OF LACTAMS and INDOLONES FROM DITHIOCARBONATES (XANTHATES)
  190497. 1994X    1719
  190498. 1722Y
  190499. 13714
  190500. RENAUD
  190501. Tet. Lett.CIALPHA THIO RADICAL, CHIRAL, REACTION WITH ALLYL STANNANE, MO CALCULATIONSK&SEE ALSO FOLLOWING PAPER PP. 1711
  190502. 1714M
  190503. 14723N
  190504. 2/28/96
  190505. ASSTEREOCHEMISTRY OF ALLYLATION OF 1
  190506. PHENYLSULFINYLETHYL and 
  190507. TRIFLUOROETHYL RADICALS
  190508. 1994X    1703
  190509. 1706Y
  190510. 13715
  190511. GARNER
  190512. Tet. Lett.
  190513. CgCHIRAL ALPHA BROMO ACRYLATE, AMINE, CONJUGATE ADDITION AND INTRAMOLECULAR N
  190514. ALKYLATION, OPPOLZER SULTAMM
  190515. 14724N
  190516. 2/28/96
  190517. AGAUXILIARY MEDIATED SYNTHESIS OF AZIRIDINE
  190518. CARBOXYLIC ACID DERIVATIVES
  190519. 1994X    1653
  190520. 1656Y
  190521. 13716
  190522. A    KIBAYASHI
  190523. INDOLIZIDINE, HYDROXAMIC ACID, OXIDATION, DIENE, CYCLOADDITION, CYCLODEHYDRATION OF AMINO ALCOHOL WITH CARBON TETRAHALIDE AND PPH3, PYRROLIDINEM
  190524. 14725N
  190525. 2/28/96
  190526. AUNEW CHIRAL ROUTE to (
  190527. SWAINSONINE VIA AN AQUEOUS ACYLNITROSO CYCLOADDITION APPROACH
  190528. 1994X    1358
  190529. 1364Y
  190530. 13717
  190531. HARMATA
  190532. CgALPHA CHLOROKETONE, LITHIUM PERCHLORATE SOLVOLYSIS TO OXALLYL CATION, FURAN CYCLOADDITION, DIHYDROFURANM
  190533. 14726N
  190534. 2/28/96
  190535. A`INTRAMOLECULAR 4 + 3 CYCLOADDITIONS OF OXALLYL CATIONS WITH FURANS.  SYNTHESIS OF CYCLOOCTANOIDS
  190536. 1994X    1241
  190537. 1242Y
  190538. 13718
  190539. SIDLER
  190540. REIDER
  190541. JOCCZAMINE, ALUMINUM ALKYUL, ALUMINUM AMIDE, ACYLATION, ME3AL PLUS ME2NHCL GIVES ME2AL(CL)NHME2M
  190542. 14727N
  190543. 2/28/96
  190544. ALUMINUM
  190545. AMINEPLEXES FOR THE CONVERSION OF CARBOXYLIC ESTERS to AMIDES.  THE NATURE OF THE SPECIES INVOLVED IN THE WEINREB AMIDE SYNTHESIS
  190546. 1994X    1231
  190547. 1233Y
  190548. 13719
  190549. JACSC
  190550. INTRAMOLECULAR ACETAL OF AMINO ACID WITH ALDEHYDE, N
  190551. ACYL IMINIUM ION, REDUCTION, ALLYL SILANE ADDITION, FRIEDEL
  190552. CRAFTS, LACTAM, HOMOQUINOLIZIDINE, TETRAHYDROAZEPINEM
  190553. 14728N
  190554. 2/28/96V-PEPTIDOMIMETIC SYNTHESIS.  FREIDINGER LACTAMSW
  190555. 1994X    2348
  190556. 2355Y
  190557. 13720
  190558. PAVLIK
  190559. JACSC]PHOTOCHEMISTRY, ELECTROCYCLIC RING CLOSURE, SHIFT OF SULFUR AROUND FOUR SIDES OF AZETINE RINGM
  190560. 14729N
  190561. 2/28/96
  190562. AqPHOTOTRANSPOSITION CHEMISTRY OF PHENYLISOTHIAZOLES and PHENYLTHIAZOLES.  1.  INTERCONVERSIONS IN BENZENE SOLUTION
  190563. 1994X    2292
  190564. 2300Y
  190565. 13721
  190566. GUINDON
  190567. COALCOHOL, ENOATE, IODINE, IODOETHERIFICATION, RADICAL REDUCTION, TETRAHYDROFURANM
  190568. 14730N
  190569. 2/28/96
  190570. AhSTEREOSELECTIVE HYDROGEN TRANSFER to ACYCLIC RADICALS.  TETRAHYDROFURANS BY IODOETHERIFICATION OF ENOATE
  190571. 1994X    1166
  190572. 1178Y
  190573. 13722
  190574. RAPOPORT
  190575. JOCCxPROLINE DERIVATIVE, DECARBOXYLATION TO IMINIUM ION, MANNICH WITH KETONE, PYRROLIDINE, 9
  190576. AZABICYCLO[4.2.1]NONANE SKELETONM
  190577. 14731N
  190578. 2/28/96
  190579. A0CONFORMATIONALLY CONSTRAINED ANALOGS OF ANATOXIN
  190580. 1994X    1058
  190581. 1066Y
  190582. 13723
  190583. MOMOSE
  190584. CvPIPERIDINE, PYRROLIDINE, INDOLIZIDINE, AMINO ALCOHOL CYCLIZATION WITH CBR4 AND PPH3, LIPASE HYDROLYSIS OF MESO DIESTERM
  190585. 14732N
  190586. 2/28/96
  190587. ASYMMETRIC SYNTHESIS OF THE INDOLIZIDINE ALKALOIDS 207A, 209B, and 235B':  6
  190588. SUBSTITUTED 2,3
  190589. DIDEHYDROPIPERIDINE
  190590. CARBOXYLATE AS A VERSATILE CHIRAL BUILDING BLOCK
  190591. 1994X
  190592. 13724
  190593. VEDEJS
  190594. JACSC6AMIDE ENOLATE, CHIRAL ANILINE, PROTONATION, ASYMMETRICM
  190595. 14733N
  190596. 2/28/96
  190597. AcDERACEMIZATION VIA HIGHLY ENANTIOSELECTIVE ENOLATE PROTONATION USING A CHIRAL ANILINE AS THE "ACID"
  190598. 1994X    2175
  190599. 2176Y
  190600. 13725
  190601. BALDWIN
  190602. JACSCh2
  190603. SILYLOXYPYRROLE, ALDEHYDE, ALDOL AT C
  190604. 5 OF PYRROLE, LACTAM, CHIRAL AMINO ACETAL AUXILIARY, PYRROLIDONEM
  190605. 14734N
  190606. 2/28/96
  190607. A3TOTAL SYNTHESIS OF (-)
  190608. LACTACYSTIN FROM R
  190609. GLUTAMATE
  190610. 1994X    2139
  190611. 2140Y
  190612. 13726
  190613. WAYMOUTH
  190614. JACSCiDIENE, ALKENE, ZIRCONOCENE, ZIRCONACYCLOPENTANE, TRANSMETALATION, ORGANOMAGNESIUM, GRIGNARD, CYCLOPENTANEM
  190615. 14735N
  190616. 2/28/96
  190617. ATMECHANISM and STEREOCHEMISTRY OF THE ZIRCONIUM
  190618. CATALYZED CYCLOMAGNESIATION OF DIENES
  190619. 1994 X    1845
  190620. 1854Y
  190621. 13727
  190622. ROKITA
  190623. JACSCPQUINONE, THIOETHER, BENZYLIC ACETATE, REDUCTION, QUINONE METHIDE, DNA ALKYLATIONM
  190624. 14736N
  190625. 2/28/96
  190626. A>ROLE OF QUINONE METHIDE IN SEQUENCE SPECIFIC ALKYLATION OF DNA
  190627. 1994X    1690
  190628. 1697Y
  190629. 13728
  190630. HAWKINS
  190631. JACSC{DIELS
  190632. ALDER CYCLOADDITION, CHIRAL DICHLOROBORANE CATALYST, 2
  190633. ARYLCYCLOHEXYL, CROTONATE, ESTER, DIENOPHILE, X
  190634. RAY STRUCTURESM
  190635. 14737N
  190636. 2/28/96
  190637. AcASYMMETRIC LEWIS ACID
  190638. DIENOPHILE COMPLEXATION:  SECONDARY ATTRACTION VERSUS CATALYST POLARIZABILITY
  190639. 1994X    1657
  190640. 1660Y
  190641. 13729
  190642. A    SHARPLESS
  190643. JACSCtQUINUCLIDINE SYNTHESIS AND MODIFICATION, N
  190644. OXIDE DEPROTONATION, REDUCTION, DIHYDROXYLATION, ASYMMETRIC, QUINUCLIDINEM
  190645. 14738N
  190646. 2/28/96
  190647. A}TOWARD AN UNDERSTANDING OF THE HIGH ENANTIOSELECTIVITY IN THE OSMIUM
  190648. CATALYZED ASYMMETRIC DIHYDROXYLATION (AD).  1.  KINETICS
  190649. 1994X    1278
  190650. 1291Y
  190651. 13730
  190652. BAEG, J.
  190653. ALPER, H.
  190654. JACSC8AZIRIDINE, CYCLOADDITION, PALLADIUM, IMIDAZOLIDINETHIONEM
  190655. 14739N
  190656. 2/28/96
  190657. AKNOVEL PALLADIUM(II)
  190658. CATALYZED CYCLIZATION OF AZIRIDINES and SULFUR DIIMIDES
  190659. 1994X    1220
  190660. 1224Y
  190661. 13731
  190662. BARRETT
  190663. J.C.S. Chem. Commun.Cl2
  190664. AZAPENTADIENYL ANION, BORONATION, ALLYL BORANE, ALDEHYDE, ALPHA AMINO ANION EQUIVALENT, BETA AMINO ALCOHOLM
  190665. 14740N
  190666. 2/28/96
  190667. A=ANTI
  190668. AMINO ALCOHOLS FROM ALLYL BORANE ADDITION to ALDEHYDES
  190669. 1994X    1053
  190670. 13732
  190671. HIEMSTRA
  190672. SPECKAMP
  190673. J.C.S. Chem. Commun.C
  190674. ACYLIMINIUM ION REACTION WITH ENOL SILANE, PALLADIUM
  190675. CATALYZED AMIDOCARBONYLATION, HECK REACTION, OXYMERCURATION TO FORM TETRAHYDROPYRAN FROM ALCOHOL AND ALKENEM
  190676. 14741N
  190677. 2/28/96
  190678. A(THE TOTAL SYNTHESIS OF RACEMIC GELSIMINE
  190679. 1994X
  190680. 13733
  190681. JOHNSON, P. A.
  190682. J.C.S. Chem. Commun.C
  190683. ACYLIMINIUM ION CYCLIZATION WITH ENOL SILANE, OXINDOLE FORMATION USING WENDER; BENZOTRIAZOLE PHOTOLYSIS / AMINYL RADICAL CYCLIZATIONK
  190684.  (2 PAPERS)M
  190685. 14742N
  190686. 2/28/96
  190687. A TOTAL SYNTHESIS OF GELSIMINE.
  190688. 1994X
  190689. 763, 765
  190690. 13734
  190691. A,BARKS, J. M.
  190692. KNIGHT, D. W.
  190693. WEINGARTEN, G. G.
  190694. J.C.S. Chem. Commun.C4IODOETHERIFICATION, ALCOHOL, ALKENE, TETRAHYDROFURANM
  190695. 14743N
  190696. 2/28/96
  190697. AVTETRAHYDROFURANS and TETRAHYDROPYRANS BY IODOCYCLIZATIONS OF 2
  190698. ALKENYLCYCLOALKAN
  190699. 1994X
  190700. 13735
  190701. MAXWELL, B. J.
  190702. TSANAKTSIDIS, J.
  190703. J.C.S. Chem. Commun.CNAMINYL RADICAL, CYCLIZATION, PYRROLIDINE, SULFENAMIDE, 2
  190704. MERCAPTOBENZOTHIAZOLEM
  190705. 14744N
  190706. 2/28/96
  190707. ABINFLUENCE OF BIS(TRIBUTYLTIN) OXIDE ON AMINYL RADICAL CYCLIZATIONS
  190708. 1994X
  190709. 13736
  190710. HONDA
  190711. J.C.S. Chem. Commun.CrAZIDE, KETONE, INTRAMOLECULAR AZA
  190712. WITTIG, STAUDINGER, IMINE, REDUCTION, REDUCTIVE AMINATION, PIPERIDINE, MITSUNOBUM
  190713. 14745N
  190714. 2/28/96
  190715. AySYNTHESIS OF NUPHAR PIPERIDINE ALKALOIDS (
  190716. ANHYDRONUPHARAMINE, (
  190717. NUPHARAMINE, (
  190718. NUPHENINE, and (+)
  190719. EPINUPHARAMINE
  190720. 1994X
  190721. 13737
  190722. SPRECHER
  190723. JACSCxSCHMIDT REARRANGEMENT OF KETONES, GOOD MECHANISTIC DISCUSSION, ARYL VERSUS MIGRATION, AMINODIAZONIUM, IMINODIAZONIUM IONM
  190724. 14746N
  190725. 2/28/96
  190726. A0THE SCHMIDT REACTION OF DIALKYL ACYLPHOSPHONATES
  190727. 1994X    1016
  190728. 1026Y
  190729. 13738
  190730. SCHEEREN
  190731. Tet. Lett.CzPYRROLE, VINYL SULFONE, CYCLOADDITION, HECK ARYLATION, RANEY NICKEL DESULFURIZATION, SULFONE REDUCTION WITH SODIUM AMALGAMK
  190732. EPIBATIDINE ANALOG MADEM
  190733. 14747N
  190734. 2/28/96
  190735. ApENDO
  190736. PHENYL
  190737. AZABICYCLO[2.2.1]HEPTANE BY HIGH PRESSURE DIELS
  190738. ALDER REACTION OF A PYRROLE WITH A VINYL SULFONE
  190739. 1994X    1299
  190740. 1300Y
  190741. 13739
  190742. DUREAULT
  190743. Tet. Lett.C
  190744. HYDROXY AZIDE ALCOHOL, PPH3 CLOSURE TO AZIRIDINE RING
  190745. OPENING WITH AZIDE AS THIOLATE, INTRAMOLECULAR RING OPENING BY NITROGEN TO GIVE PYRROLIDINEM
  190746. 14748N
  190747. 2/28/96
  190748. AE2,5
  190749. DISUBSTITUTED PYRROLIDINES FROM D
  190750. MANNITOL
  190751. DERIVED BIS AZIRIDINES
  190752. 1994X    1201
  190753. 1204Y
  190754. 13740
  190755. HIEMSTRA
  190756. SPECKAMP
  190757. Tet. Lett.CVIMIDE, REDUCTION, ASYMMETRIC, N
  190758. ACYLIMINIUM ION PRECURSOR, LACTONE, LACTAM, HEMIAMINALM
  190759. 14749N
  190760. 2/28/96
  190761. AKOXAZABOROLIDINE CATALYZED ENANTIOSELECTIVE REDUCTIONS OF CYCLIC MESO IMIDES
  190762. 1994X    1087
  190763. 1090Y
  190764. 13741
  190765. MARIANO
  190766. Tet. Lett.CVALPHA SILYL AMINE, SET
  190767. PHOTOSENSITIZATION, ALPHA AMINO RADICAL CYCLIZATION, PIPERIDINEM
  190768. 14750N
  190769. 2/28/96
  190770. KETO PIPERIDINES BY PHOTOINDUCED RADICAL CYCLIZATION OF A
  190771. SILYLAMINOENONES and YNONES
  190772. 1994X
  190773. 1002Y
  190774. 13742
  190775. MEYERS
  190776. Tet. Lett.CuPHENYLGLYCINOL
  190777. DERIVED LACTAM, LITHIUM ENOLATE ALKYLATION, LAH REDUCTION, HYDROGENOLYSIS OF BENZYL GROUP, PYRROLIDINEM
  190778. 14751N
  190779. 2/28/96
  190780. ASSYNTHESIS OF ENANTIOMERICALLY PURE 3
  190781. SUBSTITUTED and 3,3
  190782. DISUBSTITUTED PYRROLIDINES
  190783. 1994X
  190784. 13743
  190785. Tet. Lett.C]DIHYDROPYRANS (BIS), ALPHA HYDROXY ACID PROTECTION AS DIOXANONE SPIROKETAL, ALKYLATION, ALDOLKeSEE THE FOLLOWING PAPERS FOR SELECTIVE PROTECTION OF CARBOHYDRATE DIOLS WITH DISPIROKETAL ("DISPOKE")M
  190786. 14752N
  190787. 2/28/96
  190788. AYALKYLATION and ALDOL REACTION OF LACTIC ACID and GLYCOLIC ACID ENOLATES VIA DISPIROKETALS
  190789. 1994 X
  190790. 13744
  190791. MARTIN
  190792. Tet. Lett.CiENAMIDE, DIENE, DIELS
  190793. ALDER, MOLYBDENUM CARBENE CATALYZED OLEFIN METATHESIS, ALKENE, PYRROLIDINE, AZOCINEM
  190794. 14753N
  190795. 2/28/96
  190796. AQAPPROACH to MANZAMINE A USING INTRAMOLECULAR DIELS
  190797. ALDER and GRUBBS FU METATHESIS
  190798. 1994 X
  190799. 13745
  190800. GANEM
  190801. JACSCoGLYCOPROTEIN BIOSYNTHESIS INHIBITORS, ACYLNITROSO CYCLOADDITION WITH DIENE, MANNOSTATIN SYNTHESIS, CYCLOPENTANEM
  190802. 14754N
  190803. 2/28/96
  190804. APMANNOSTATIN A and DERIVATIVES:  NEW FAMILY OF GLYCOPROTEIN PROCESSING INHIBITORS
  190805. 1994X
  190806. 13746
  190807. WONG 
  190808. SHARPLESS
  190809. JACSC
  190810. ALKENE, OSMIUM, DIHYDROXYLATION, ASYMMETRIC, ALPHA, BETA
  190811. DIHYDROXYALDEHYDE, 1,2
  190812. BIS(HYDROXYMETHYL)BENZENE AS ALDEHYDE PROTECTING GROUP, ACETAL, ENZYMATIC ALDOL, CARBOHYDRATEKb1,2
  190813. BENZENEDIMETHANOL PROTECTING GROUP FOR ALDEHYDES:  KIBAYASHI, TETRAHEDRON LETT 1989, 30, 4165.M
  190814. 14755N
  190815. 2/28/96
  190816. ALCARBOHYDRATES BY TANDEM SHARPLESS DIHYDROXYLATION and ENZYME
  190817. CATALYZED ALDOL
  190818. 1994X
  190819. 13747
  190820. SCHLEYER
  190821. JACSC
  190822. MP2 (FULL) MOLECULAR ORBITAL CALCULATIONS ON ORGANOLITHIUM AND OTHER ORGANOMETALS WERE FOUND TO BE BEST.  SEE ALSO SCHLEYER, ORGANOMETALLICS, 1993, 12, 853.  MNDO COMPARED.  GAUSSIAN 92M
  190823. 14756N
  190824. 2/28/96
  190825. A@STRUCTURE OF BENZYLPOTASSIUM and BENZYLRUBIDIUM (X
  190826. RAY, NMR, MO)
  190827. 1994X
  190828. 13748
  190829. A    SINGLETON
  190830. Tet. Lett.C^VINYL STANNANE, BROMO BORANE EXCHANGE, VINYL BORANE, CYCLOADDITION, OXIDATION TO ALCOHOL, DIOLM
  190831. 14757N
  190832. 2/28/96
  190833. ANVINYL BORANES AS TRANS
  190834. DIHYDROXYETHYLENE EQUIVALENTS FOR DIELS
  190835. ALDER REACTIONS
  190836. 1994X
  190837. 13749
  190838. BANKS
  190839. Tet. Lett.CGAZIDE, THERMOLYSIS, FLASH VACUUM, NITRENE, C
  190840. H INSERTION, OXAZOLIDINONEM
  190841. 14758N
  190842. 2/28/96
  190843. AqNEW OXAZOLIDINONE CHIRAL AUXILIARIES VIA INTRAMOLECULAR C
  190844. H INSERTION OF NITRENE DERIVED FROM FVT OF AZIDOFORMATE
  190845. 1994X
  190846. 13750
  190847. ROBL, J. A.
  190848. Tet. Lett.C8IMINIUM ION, ACYLIMINIUM ION, AMINO ACID, ALKENE, LACTAMM
  190849. 14759N
  190850. 2/28/96
  190851. ARPEPTIDOMIMETIC 7,6
  190852.  and 7,5
  190853. FUSED BICYCLIC LACTAMS VIA N
  190854. ACYLIMINIUM ION CHEMISTRY
  190855. 1994 X
  190856. 13751
  190857. MARSON
  190858. Tet. Lett.C1AMIDE, ALKENE, ACID CATALYZED CYCLIZATION, LACTAMM
  190859. 14760N
  190860. 2/28/96
  190861. A@LACTAMS BY ACID CATALYZED RING CLOSURE OF b,g
  190862. UNSATURATED AMIDES
  190863. 1994X
  190864. 13752
  190865. ZARD 
  190866. Tet. Lett.C`OXIME BENZOATE, TRIBUTYLFIN HYDRIDE, IMINYL RADICAL, ALKENE, CYCLIZATION, PYRROLINE, PYRROLIDINEM
  190867. 14761N
  190868. 2/28/96
  190869. A=IMINYL RADICALS BY STANNANE MEDIATED CLEAVAGE OF OXIME ESTERS
  190870. 1994X
  190871. 13753
  190872. COHEN 
  190873. Tet. Lett.C?ORGANOLITHIUM, ACYLATION, CARBOXYLATE, CERIUM, KETONE FORMATIONKfMONO
  190874. ADDITION TO LACTONES ALSO FACILITATED BY CECL3 (SEE PREVIOUS WORK BY COHEN, JACS 1990, 112, 6389)M
  190875. 14762N
  190876. 2/28/96
  190877. A_CERIUM (III) CHLORIDE FACILITATES FORMATION OF KETONES FROM CARBOXYLIC ACIDS and ORGANOLITHIUMS
  190878. 1994X
  190879. 13754
  190880. ESKER, J. L.
  190881. NEWCOMB, M.
  190882. Adv. Het. Chem.CjRADICAL, NITROGEN, AMINYL, CYCLIZATION, PYRROLIDINE, REVIEW
  190883. REVIEW, AMINYL RADICALS, PYRROLIDINE SYNTHESISM
  190884. 14763N
  190885. 2/28/96
  190886. AjTHE GENERATION OF NITROGEN RADICALS and THEIR CYCLIZATIONS FOR THE CONSTRUCTION OF THE PYRROLIDINE NUCLEUS
  190887. 1993 X
  190888. 13755
  190889. Tet. Lett.CiALPHA ALKOXY RADICAL CYCLIZATION, TETRAHYDROPYRAN FORMATION, BU3SNH ADDITION TO ALDEHYDE, TETRAHYDROFURANM
  190890. 14764N
  190891. 2/28/96
  190892. AEFUSED OXACYCLE SYNTHESIS VIA RADICAL CYCLIZATION OF b
  190893. ALKOXYACRYLATES
  190894. 1994 X
  190895. 13756
  190896. WUSTROW
  190897. SMITH
  190898. Tet. Lett.CW ALLYLIC CATION, REDUCTION, SILANE, DEOXYGENATION, LITHIUM PERCHLORATE, PEARSON, GRIECOM
  190899. 14765N
  190900. 2/28/96
  190901. AqSELECTIVE DEOXYGENATION OF ALLYLIC ALCOHOLS and ACETATES BY LITHIUM PERCHLORATE PROMOTED TRIETHYLSILANE REDUCTION
  190902. 1994X
  190903. 13757
  190904. MCDONALD
  190905. Tet. Lett.Ce3
  190906. METHOXY)PHENYL
  190907. DIOXOLANE PROTECTING GROUP FOR ALDEHYDES AND KETONES, OXIDATIVE CLEAVAGE, DDQM
  190908. 14766N
  190909. 2/28/96
  190910. ACAN OXIDATIVELY REMOVABLE PROTECTING GROUP FOR ALDEHYDES and KETONES
  190911. 1994X
  190912. 13758
  190913. LAPORTA
  190914. B    SynthesisC
  190915. AZIRIDINE, THERMOLYSIS, ELECTROCYCLIC RING
  190916. OPENING, AZOMETHINE YLIDE, ALKYNE, CYCLOADDITION, 3
  190917. PYRROLINE, OXIDATION, DDQ, PYRROLEM
  190918. 14767N
  190919. 2/28/96
  190920. AtMETHYL 3
  190921. TRIFLUOROMETHYL
  190922. PYRROLE
  190923. CARBOXYLATES BY DIPOLAR CYCLOADDITION OF AZOMETHINE YLIDES WITH ALKYNES
  190924. 1994 X
  190925. 13759
  190926. FIORAVANTI 
  190927. PELLACANI
  190928. TetrahedronCUALKENE AMINATION, AZIRIDINE FORMATION, ARENESULFONOXYAMINE, HOFFMAN, AZEPINE, NITRENEM
  190929. 14768N
  190930. 2/28/96
  190931. AwIMPROVED AMINATION BY ETHYL N
  190932. NITROPHENYL) SULFONYL]OXYCARBAMATE IN THE PRESENCE OF INORGANIC OXIDES OR CARBONATES
  190933. 1994X    3829
  190934. 3834Y
  190935. 13760
  190936. BRUCKNER
  190937. TetrahedronCZ[2,3]
  190938. WITTIG REARRANGEMENT, ALLYL ANION, SULFIDE REDUCTIVE CLEAVAGE, LITHIUM NAPHTHALENIDEM
  190939. 14769N
  190940. 2/28/96
  190941. AwGEOMETRY OF CARBANIONIC MOIETY INFUENCES DIASTEREOSELECTIVITY OF [2,3]
  190942. WITTIG REARRANGEMENT OF LITHIATED DIALLYL ETHERS
  190943. 1994 X    3687
  190944. 3708Y
  190945. 13761
  190946. MURAOKA
  190947. MOMOSE
  190948. Tetrahedron:  Asymm.CxPHOTOCHEMICAL BETA
  190949. CLEAVAGE OF BETA AMINO KETONE, ASYMMETRIC DEPROTONATION, ENOLATE, ACYLATION, INDOLIZIDINE, PIPERIDINEM
  190950. 14770N
  190951. 2/28/96
  190952. AwNORRISH TYPE I PHOTOCLEAVAGE OF A 9
  190953. AZABICYCLO[3.3.1]NONAN
  190954. ONE:  ENANTIOSELECTIVE SYNTHESIS OF (
  190955. INDOLIZIDINE 223AB
  190956. 1994 X
  190957. 13762
  190958. LEBLANC
  190959. JOCC`ELECTRON RICH ARENE, AMINATION WITH AZODICARBOXYLATE, INDOLE, 3
  190960. AMINOINDOLE, ZINC SALT CATALYZEDM
  190961. 14771N
  190962. 2/28/96
  190963. A=AMINATION OF ARENES WITH ELECTRON
  190964. DEFICIENT AZODICARBOXYLATES
  190965. 1994X
  190966. 13763
  190967. HAWKINS
  190968. CHIRAL AMMONIA EQUIVALENT, CONJUGATE ADDITION TO ENOATES, DEPROTECTION BY HYDROGENOLYSIS OF BENZYL AMINE OF 3,5
  190969. DIHYDRO
  190970. DINAPHTH[2,1
  190971. C:1',2'
  190972. E] AZEPINE, DAVIESKvSEE ALSO DAVIES, TETRAHEDRON:  ASYMMETRY 1994, 5, 35 FOR SIMILAR APPROACH USING N
  190973. BENZYL
  190974. ALPHA
  190975. METHYLBENZYLAMINE ANIONM
  190976. 14772N
  190977. 2/28/96
  190978. A4ASYMMETRIC SYNTHESIS OF A
  190979. SUBSTITUTED b-AMINO ESTERS
  190980. 1994X
  190981. 13764
  190982. AMINE, ENONE, PHOTOCHEMICAL H ABSTRACTION, ALPHA AMINO RADICAL, CONJUGATE ADDITION, LACTAM FORMATION, PYRROLIDINONE, PYRROLIZIDINE, INDOLIZIDINE, SPIRO PYRROLIDINESM
  190983. 14773N
  190984. 2/28/96
  190985. ARPHOTOCATALYZED MULTIPLE ADDITIONS OF AMINES to A,b-UNSATURATED ESTERS and NITRILES
  190986. 1994X
  190987. 13765
  190988. HOYE 
  190989. JOCCuCYCLIC SULFATE, ENOLATE, KETONE, ESTER, AMIDE, NITRILE, LACTONE, EPOXIDE EQUIVALENT, ALKYLATION, EVANS' OXAZOLIDINONEM
  190990. 14774N
  190991. 2/28/96
  190992. AsENOLATE and OTHER CARBON NUCLEOPHILE ALKYLATION REACTIONS USING 1,2
  190993. CYCLIC SULFATES AS TERMINAL EPOXIDE EQUIVALENTS
  190994. 1994X
  190995. 13766
  190996. INDOLE, AZIRIDINE, RING OPENING, TRYPTOPHAN DERIVATIVES, LEWIS ACID PROMOTED, REGIOSELECTIVITY COMPLEMENTARY, MNDO CALCULATIONSM
  190997. 14775N
  190998. 2/28/96
  190999. A<OPENING OF AZIRIDINES WITH N
  191000. METHYLINDOLE.  REGIOSELECTIVITY
  191001. 1994X
  191002. 13767
  191003. DANISHEFSKY
  191004. JOCCbPALLADIUM, INTRAMOLECULAR HECK ARYLATION OF ENOL ETHERS, HEXAHYDRO OXAZINE, ARYL IODIDE, FR 900482M
  191005. 14776N
  191006. 2/28/96
  191007. A_A REMARKABLE STEREOCHEMICAL INVERSION IN SOME HECK ARYLATION REACTIONS.  A MECHANISTIC PROPOSAL
  191008. 1994X
  191009. 13768
  191010. FUCHS
  191011. =C[AMIDE, LACTAM, THIOAMIDES, THIOLACTAM, THIONATION, ALTERNATIVE TO LAWESSON'S REAGENT, TMS2SK
  191012. ACTIVATE AMIDE FIRST WITH PHOSPHORUS OXYCHLORIDE, TRIPHOSGENE, OR OXALYL CHLORIDE.  WORKS ON PRIMARY, SECONDARY, OR TERTIARY AMIDESM
  191013. 14777N
  191014. 2/28/96
  191015. A[CONVERSION OF AMIDES AND LACTAMS to THIOAMIDES and THIOLACTAMS USING HEXAMETHYLDISILATHIANE
  191016. 1994X
  191017. 13769
  191018. MARSON
  191019. JOCCON
  191020. ACYLIMINIUM ION, ALKENE, CARBOCATION, CATIONIC CYCLIZATION, DELTA LACTAM, PPEM
  191021. 14778N
  191022. 2/28/96
  191023. A\5,6
  191024. DIHYDRO
  191025. 2(1H)
  191026. PYRIDINONES FROM PPE CYCLIZATIONS OF b,g
  191027. UNSATURATED AMIDES WITH ALDEHYDES
  191028. 1994X
  191029. 13770
  191030. MARSON
  191031. JOCCxN
  191032. ACYLIMINIUM ION, ALKENE, ELECTROPHILIC AROMATIC SUBSTITUTION, LACTAM, CYCLOPENTANE, BENZO FUSED, SECONDARY CARBOCATIONM
  191033. 14779N
  191034. 2/28/96
  191035. A"g-LACTAMS BY CATIONIC CYCLIZATIONS
  191036. 1994X
  191037. 13771
  191038. BeakB
  191039. CARBAMATES, ALPHA METALATION, ALPHA AMINO ANION EQUIVALENT, INTRAMOLECULAR ALKYLATION, PYRROLIDINE, PIPERIDINE, CYCLOPROPANE, AZIRIDINE, EPOXIDE, OXIRANE, PYRROLIZIDINEM
  191040. 14780N
  191041. 2/28/96
  191042. CYCLIZATION OF A-AMINO ANIONS
  191043. 1994X
  191044. 13772
  191045. LEWIS, J. R.
  191046. Nat. Prod. Rep.
  191047. AC+REVIEW, AMARYLLIDACEAE, SCELETIUM ALKALOIDSM
  191048. 14781N
  191049. 2/28/96
  191050. A&AMARYLLIDACEAE and SCELETIUM ALKALOIDS
  191051. 1993X
  191052. 13773
  191053. JOHNSON, C. D.
  191054. Acc. Chem. Res.C7REVIEW, BALDWIN'S RULES, STEREOELECTRONIC, RING CLOSUREM
  191055. 14782N
  191056. 2/28/96
  191057. AbSTEREOELECTRONIC EFFECTS IN THE FORMATION OF 5
  191058.  and 6
  191059. MEMBERED RINGS:  THE ROLE OF BALDWIN'S RULES
  191060. 1993X
  191061. 13774
  191062. TIETZE
  191063. ZIRCONOCENE
  191064. BENZYNE COMPLEX, ALLYL AMINE INSERTION, INDOLINE, ZIRCONACYCLOPENTANE, BUCHWALD METHOD, INTRAMOLECULAR HECK REACTION, PALLADIUM, INDOLEM
  191065. 14783N
  191066. 2/28/96
  191067. AGSYNTHESIS OF CPI, RELATED to CC
  191068. 1065, BY ZIRCONOCENE and HECK CHEMISTRY
  191069. 1994X
  191070. 13775
  191071. RESSIG
  191072. JOCCzALLENE, ORGANOLITHIUM, ADDITION TO ALPHA AMINO ALDEHYDES, TBUOK PROMOTED CYCLIZATION OF ALLENIC ALCOHOL TO DIHYDROFURANONEM
  191073. 14784N
  191074. 2/28/96
  191075. AQ3(2H)
  191076. DIHYDROFURANONES BY ADDITION OF LITHIATED METHOXYALLENE to CHIRAL ALDEHYDES
  191077. 1994 X
  191078. 13776
  191079. OVERALL 
  191080. JOCCDSUBSTITUTION, E.G. PH2NCH2SPH + TBULI = PH2NCH2TBU VIA PH2NCH(LI)TBUM
  191081. 14785N
  191082. 2/28/96
  191083. AmCARBON
  191084. SULFUR BOND CLEAVAGES OF SUBSTITUTED AMINOMETHYL SULFIDES WITH ORGANOLITHIUM REAGENTS:  AMINO CARBENES
  191085. 1994X
  191086. 13777
  191087. GARNER
  191088. AZIRIDINE, 2
  191089. ACYL, CHIRAL AUXILIARY, THERMAL RING OPENING, DIPOLAR CYCLOADDITION, PYRROLIDINE, ASYMMETRIC, GLYCINE IMINE, PROTOTROPIC SHIFTKKSEE CURRAN TETRAHEDRON 1993, 49, 293 FOR REVIEW OF USE OF OPPOLZER'S SULTAMM
  191090. 14786N
  191091. 2/28/96
  191092. AVAUXILIARY CONTROLLED 1,3
  191093. DIPOLAR CYCLOADDITIONS OF CHIRAL STABILIZED AZOMETHINE YLIDES
  191094. 1994X
  191095. 13778
  191096. BeakB
  191097. JACSCWCOMPLEX
  191098. INDUCED PROXIMITY EFFECT, ALPHA AMINO ANION, UREA, DEPROTONATION, ORGANOLITHIUMM
  191099. 14787N
  191100. 2/28/96
  191101. AYCIPE:  EVIDENCE FOR A COMPLEX AS THE REACTION PATHWAY OF A' LITHIATION OF A BENZYLIC UREA
  191102. 1994X
  191103. 13779
  191104. STANG
  191105. JACSClALKYNYL STANNANE, IODONIUM SALT, SULFINATE ADDITION, VINYL CARBENE, INSERTION, CYCLOPENTENONE, PYRROLIDINONEM
  191106. 14788N
  191107. 2/28/96
  191108. AGCYCLOPENTENONES and PYRROLIDINONES VIA INTRAMOLECULAR CARBENE INSERTION
  191109. 1994X
  191110. 13780
  191111. BANERT
  191112. JACSCUAZIRINE, VINYL AZIDE, ALLENE PHOTOLYSIS, MATRIX ISOLATION, IR, AB INITIO CALCULATIONSM
  191113. 14789N
  191114. 2/28/96
  191115. ASREACTIONS OF UNSATURATED AZIDES.  II.  DIRECT OBSERVATION OF 2
  191116. METHYLENE
  191117. AZIRINE
  191118. 1994X
  191119. 13781
  191120. FALCK 
  191121. JACSCXSTANNANE, TIN, ALPHA ALKOXY, AMINO, PALLADIUM, CROSS
  191122. COUPLING, ACYLATION, KETONE, COPPERM
  191123. 14790N
  191124. 2/28/96
  191125. ArSTEREOSPECIFIC PALLADIUM / COPPER COCATALYZED CROSS
  191126. COUPLING OF A-ALKOXY and A-AMINO STANNANES WITH ACYL CHLORIDES
  191127. 1994X
  191128. 116  
  191129. 13782
  191130. GANEM
  191131. BiochemistryC
  191132. GLYCOSIDASE, AMIDRAZONEM
  191133. 14791N
  191134. 2/28/96
  191135. A]AMIDRAZONE ANALOGUES OF D
  191136. RIBOFURANOSE AS TRANSITION STATE INHIBITORS OF NUCLEOSIDE HYDROLASE
  191137. 1994X    3994
  191138. 4000Z
  191139. 13783
  191140. MAJETICH
  191141. Res. Chem. Intermed.CcMICROWAVE, REVIEW, DIELS
  191142. ALDER, CLAISEN REARRANGEMENT, ENE, SUBSTITUTION, OXIDATION, ESTERIFICATIONK4THIS ENTIRE ISSUE IS DEVOTED TO MICROWAVE TECHNIQUESM
  191143. 14792N
  191144. 2/28/96
  191145. A7APPLICATIONS OF MICROWAVE ACCELERATED ORGANIC CHEMISTRY
  191146. 1994 X
  191147. 13784
  191148. CRAIG
  191149. Tet. Lett.CsALPHA THIOETHER, OXONIUM ION, ENOL SILANE, CYCLIZATION, TETRAHYDROFURAN, TETRAHYDROPYRAN, OXYGEN VERSION OF MANNICHM
  191150. 14793N
  191151. 2/28/96
  191152. AFTETRAHYDROFURANS BY OXONIUM ION CYCLIZATIONS WITH KETENE SILYL ACETALS
  191153. 1993X    8539
  191154. 8542Z
  191155. 13785
  191156. MOODY 
  191157. Tet. Lett.Cs3
  191158. HYDROXYMETHYLINDOLE, INDOLE, IONIZATION TO CATION, CYCLOADDITION WITH ALKENE, CYCLOPENTANE FORMATION, IMINIUM IONM
  191159. 14794N
  191160. 2/28/96
  191161. A^SYNTHESIS OF CYCLOPENTA[B]INDOLES BY FORMAL [3+2]
  191162. ADDITION OF INDOLYLMETHYL CATIONS to ALKENES
  191163. 1994X    8527
  191164. 8530Z
  191165. 13786
  191166. MICHAEL
  191167. Tet. Lett.C>HECK, PALLADIUM, INDOLE SYNTHESIS, ENAMIDE, MITOMYCIN SKELETONM
  191168. 14795N
  191169. 2/28/96
  191170. ASPYRROLO[1,2
  191171. A]INDOLES BY INTRAMOLECULAR HECK REACTION OF N
  191172. BROMOARYL) ENAMINONES
  191173. 1993X    8365
  191174. 8368Z
  191175. 13787
  191176. KANEMASA
  191177. Tet. Lett.C]GLYCINE ENOLATE, IMINE, ALDOL, BETA HYDROXY AMINO ACID, ASYMMETRIC, ENOLATE, 2
  191178. AZAALLYL ANIONM
  191179. 14796N
  191180. 2/28/96
  191181. AdASYMMETRIC ANTI
  191182. SELECTIVE ALDOL REACTIONS OF TITANIUM ENOLATES DERIVED FROM N
  191183. ALKYLIDENEGLYCINAMIDES
  191184. PX    8293
  191185. 8296Z
  191186. 13788
  191187. PEARSON
  191188. Tet. Lett.CiINDOLIZIDINE, QUINOLIZIDINE, SWAINSONINE, CASTANOSPERMINE, AZIDE, REDUCTION, EPOXIDE, DOUBLE N
  191189. ALKYLATIONM
  191190. 14797N
  191191. 2/28/96
  191192. AeNOVEL POLYHYDROXYLATED QUINOLIZIDINES:  RING
  191193. EXPANDED ANALOGS OF GLYCOSIDASE INHIBITORY INDOLIZIDINES
  191194. 1993X    8221
  191195. 8224Z
  191196. 13789
  191197. KRAFFT
  191198. Tet. Lett.C
  191199. CLAISEN REARRANGEMENT, CHELATION OF MAGNESIUM ENOLATE TO ETHER IN SIDE
  191200. CHAIN, ALTERATION OF GEOMETRICAL STEREOSELECTIVITY, ALKENEM
  191201. 14798N
  191202. 2/28/96V'A LIGAND ASSISTED CLAISEN REARRANGEMENTW
  191203. 1994X    8209
  191204. 8212Z
  191205. 13790
  191206. STILLE
  191207. Tet. Lett.
  191208. SCvBETA KETOESTER, IMINE, ALPHA, BETA
  191209. UNSATURATED ACID CHLORIDE, AZA
  191210. ANNULATION, CYCLIC ENAMIDE, PIPERIDINE, INDOLIZIDINEM
  191211. 14799N
  191212. 2/28/96
  191213. AnCONFORMATIONALLY RESTRICTED b-AMINO ACID ISOSTERES PREPARED THROUGH REGIOSELECTIVELY CONTROLLED AZA
  191214. ANNULATION
  191215. 1993X    8197
  191216. 8200Z
  191217. 13791
  191218. NAKAI 
  191219. Tet. Lett.CfTIN
  191220. LITHIUM EXCHANGE, ALPHA ALKOXY STANNANE, ORGANOLITHIUM, WITTIG REARRANGEMENT, 1,2
  191221. SHIFT, DIRADICALM
  191222. 14800N
  191223. 2/28/96
  191224. Ay[1,2]
  191225. WITTIG REARRANGEMENT OF A
  191226. ALKOXY ALKYLLITHIUMS:  INVERSION AT LI
  191227. BEARING TERMINUS and RETENTION AT MIGRATING CENTER
  191228. 1993 X    8139
  191229. 8142Z
  191230. 13792
  191231. Tet. Lett.CETETRAZOLE FROM NITRILE, TRIMETHYLSILYLAZIDE, AZIDE, TRIMETHYLALUMINUMM
  191232. 14801N
  191233. 2/28/96
  191234. AjA NEW METHOD FOR THE PREPARATION OF TETRAZOLES FROM NITRILES USING TRIMETHYLSILYLAZIDE / TRIMETHYLALUMINUM
  191235. 1993 X    8011
  191236. 8014Z
  191237. 13793
  191238. FALCK 
  191239. TetrahedronC
  191240. PALLADIUM AND COPPER CO
  191241. CATALYZED ACYLATION OF ALPHA ALKOXY STANNANE, TIN, RETENTION OF CONFIGURATION, COPPER ASSISTS THE TRANSMETALATION, LIEBESKIND, STILLE, FARINAK
  191242. SEE ALSO JACS 1994, 116, 1
  191243. 14802N
  191244. 2/28/96
  191245. AdSTEREOSPECIFIC A-ALKOXYSTANNANE COUPLINGS WITH ACYL CHLORIDES:  TOTAL SYNTHESIS OF (+)
  191246. GONIOFUFURONE
  191247. 1993 X    8007
  191248. 8010Z
  191249. 13794
  191250. WALLING, CHEVES
  191251. BBProfiles, Pathways and Dreams: Autobiographies of Eminent ChemistsC
  191252. A REVIEW
  191253. A@AMERICAN CHEMICAL SOCIETY: WASHINGTON, DC
  191254. JEFFREY I. SEEMAN, ED.
  191255. 14803N
  191256. 2/28/96
  191257. FIFTY YEARS OF FREE RADICALS 
  191258. 13795
  191259. A!PATAI, SAUL
  191260. RAPPOPORT, ZVI, EDS. 
  191261. B"The Chemistry of Functional GroupsC
  191262. A REVIEWK
  191263. WILEY: CHICHESTER, U. K.M
  191264. 14804
  191265. 2/28/96
  191266. ABSUPPLEMENT S: THE CHEMISTRY OF SULFUR
  191267. CONTAINING FUNCTIONAL GROUPS
  191268. 13796
  191269. HUISGEN, ROLF
  191270. A REVIEWM
  191271. 14805N
  191272. 2/28/96
  191273. A"THE ADVENTURE PLAYGROUND ON THE . 
  191274. 13797
  191275. HASLAM, EDWIN
  191276. A REVIEWK
  191277. WILEY: CHICHESTER, U.K.M
  191278. 14806N
  191279. 2/28/96
  191280. A+SHIKIMIC ACID. METABOLISM and METABOLITES. 
  191281. 13798
  191282. CASY, ALAN F. 
  191283. A REVIEWK
  191284. PLENUM: NEW YORKM
  191285. 14807N
  191286. 2/28/96
  191287. A\THE STERIC FACTOR IN MEDICINAL CHEMISTRY. DISSYMMETRIC PROBES OF PHARMACOLOGICAL RECEPTORS. 
  191288. 13799
  191289. BLOMBERG, CORNELIS
  191290. A REVIEWKb(REACTIVITY AND STRUCTURE. CONCEPTS IN ORGANIC CHEMISTRY, VOL. 31). SPRINGERVERLAG: BERLIN, 1993. M
  191291. 14808N
  191292. 2/28/96
  191293. A4THE BARBIER REACTION and RELATED ONE
  191294. STEP PROCESSES 
  191295. 13800
  191296. BARTON, Derek H. R.
  191297. A REVIEWK-CAMBRIDGE UNIVERSITY PRESS: CAMBRIDGE, U.K., M
  191298. 14809N
  191299. 2/28/96
  191300. A*HALF A CENTURY OF FREE RADICAL CHEMISTRY. 
  191301. 13801
  191302. UEMURA, MOTOKAZU
  191303. Rev. on Heteroatom Chem.C
  191304. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191305. 14810N
  191306. 2/28/96
  191307. A:CHIRAL (h6
  191308. ARENE)CHROMIUM COMPLEXES IN ORGANIC SYNTHESIS. 
  191309. 1994Y
  191310. 13802
  191311. OKUBO, MASAO
  191312. MATSUO, KOJI
  191313. Rev. on Heteroatom Chem.C
  191314. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191315. 14811N
  191316. 2/28/96
  191317. MG REAGENTS: VARIETY OF REACTION MODES FOR C
  191318. N AND N
  191319. N BOND FORMATION
  191320. REACTIVITY OF N
  191321. MG and C
  191322. MG REAGENTS SYSTEMATIZED IN TERMS OF RELATIVE SINGLE
  191323. ELECTRON TRANSFER EFFICIENCY. 
  191324. 1994Y
  191325. 13803
  191326. TANAKA, KAZUHIKO
  191327. Rev. on Heteroatom Chem.C
  191328. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191329. 14812N
  191330. 2/28/96
  191331. A[STEREOFACE DIFFERENTIATION IN ASYMMETRIC SYNTHESIS USING CHIRAL 3
  191332. AMINO
  191333. HYDROXYBORNANES. 
  191334. 1994Y
  191335. 13804
  191336. FUCHIGAMI, TOSHIO
  191337. Rev. on Heteroatom Chem.C
  191338. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191339. 14813N
  191340. 2/28/96
  191341. A?SELECTIVE ANODIC PARTIAL FLUORINATION OF HETEROATOM COMPOUNDS. 
  191342. 1994Y
  191343. 13805
  191344. UMEMOTO, TERUO
  191345. Rev. on Heteroatom Chem.C
  191346. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191347. 14814N
  191348. 2/28/96
  191349. A+RECENT DEVELOPMENT OF FLUORINATING AGENTS. 
  191350. 1994Y
  191351. 13806
  191352. TROEV, KOLJO
  191353. Rev. on Heteroatom Chem.C
  191354. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191355. 14815N
  191356. 2/28/96
  191357. AMDIALKYL HYDROGEN PHOSPHONATES. 2. SUBSTITUTION REACTIONS AT PHOSPHORUS ATOM. 
  191358. 1994Y
  191359. 13807
  191360. A$MEMMESHEIMER, HOLGER
  191361. REGITZ, MANFRED
  191362. Rev. on Heteroatom Chem.C
  191363. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191364. 14816N
  191365. 2/28/96
  191366. PHOSPHIRENES: SYNTHESIS and PREPARATIVE SIGNIFICANCE IN ORGANOPHOSPHORUS CHEMISTRY. 
  191367. 1994Y
  191368. 13808
  191369. OGAWA, AKIYA
  191370. SONODA , NOBORU
  191371. Rev. on Heteroatom Chem.C
  191372. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191373. 14817N
  191374. 2/28/96
  191375. AESYNTHETIC UTILITY OF SELENIUM
  191376. CARBON MONOXIDE
  191377. WATER REACTION SYSTEM. 
  191378. 1994Y
  191379. 13809
  191380. RYASHENTSEVA, MARAGARITA A. 
  191381. Rev. on Heteroatom Chem.C
  191382. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191383. 14818N
  191384. 2/28/96
  191385. AUCATALYTIC SYNTHESIS OF THIOPHENE and ALKYLTHIOPHENES VIA HETEROCYCLIZATION REACTION. 
  191386. 1994Y
  191387. 13810
  191388. LOZACH, NOEL
  191389. Rev. on Heteroatom Chem.C
  191390. A REVIEWK(SHIGERU OAE, ED., MYU K.K.: TOKYO, JAPANM
  191391. 14819N
  191392. 2/28/96
  191393. A.FACTS and WORDS IN HETEROATOMIC NOMENCLATURE. 
  191394. 1994Y
  191395. 13811
  191396. CHAKRABORTY, D. P. 
  191397. B!The Alkaloids. Chem. & Pharmacol.C
  191398. A REVIEWK2GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORKM
  191399. 14820N
  191400. 2/28/96
  191401. A.CHEMISTRY and BIOLOGY OF CARBAZOLE ALKALOIDS. 
  191402. 1993Y
  191403. 13812
  191404. A!TAKAHATA, HIROKI
  191405. MOMOSE, TAKEFUMI
  191406. iB!The Alkaloids. Chem. & Pharmacol.C
  191407. A REVIEWK2GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORKM
  191408. 14821N
  191409. 2/28/96V
  191410. SIMPLE INDOLIZIDINE ALKALOIDS. W
  191411. 1993Y
  191412. 13813
  191413. A'ROBINS, RICHARD J.
  191414. WALTON, NICHOLAS J. 
  191415. B!The Alkaloids. Chem. & Pharmacol.C
  191416. A REVIEWK2GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORKM
  191417. 14822N
  191418. 2/28/96
  191419. A'THE BIOSYNTHESIS OF TROPANE ALKALOIDS. 
  191420. 1993Y
  191421. 13814
  191422. A LAUNASMAA, MAURI
  191423. TAMMINEN, TARJA
  191424. B!The Alkaloids. Chem. & Pharmacol.C
  191425. A REVIEWK2GEOFFREY A. CORDELL, ED., ACADEMIC PRESS: NEW YORKM
  191426. 14823N
  191427. 2/28/96V
  191428. THE TROPANE ALKALOIDS. W
  191429. 1993Y
  191430. 13815
  191431. A/GORDON, M. S.
  191432. FRANCISCO, J. S.
  191433. SCHLEGEL, H. B. 
  191434. Adv. Silicon Chem.C
  191435. A REVIEWK/GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CTM
  191436. 14824
  191437. 2/28/96
  191438. AxTHEORETICAL INVESTIGATIONS OF THE THERMOCHEMISTRY and THERMAL DECOMPOSITION OF SILANES, HALOSILANES, and ALKYLSILANES.  
  191439. 1993Y
  191440. 13816
  191441. DAMRAUER, ROBERT
  191442. Adv. Silicon Chem.C
  191443. A REVIEWK/GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CTM
  191444. 14825N
  191445. 2/28/96
  191446. A=GAS PHASE STUDIES ON THE NEGATIVE ION CHEMISTRY OF SILICON.  
  191447. 1993Y
  191448. 13817
  191449. A$HUDRLIK, PAUL F.
  191450. HUDRLIK, ANNE M. A.
  191451. Adv. Silicon Chem.C
  191452. A REVIEW
  191453. nK/GERALD L. LARSON, ED., JAI PRESS: GREENWICH, CTM
  191454. 14826N
  191455. 2/28/96
  191456. EPOXYSILANES. 
  191457. 1993Y
  191458. 13818
  191459. MASUYAMA, YOSHIRO
  191460. Adv. Metal-Org. Chem.C
  191461. A REVIEWK2LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CTM
  191462. 14827N
  191463. 2/28/96
  191464. AHPALLADIUM
  191465. CATALYZED CARBONYL ALLYLATION VIA p
  191466. ALLYLPALLADIUM COMPLEXES. 
  191467. 1994Y
  191468. 13819
  191469. A%MURAHASHI, SHUN
  191470. NAOTA, TAKESHI. 
  191471. Adv. Metal-Org. Chem.C
  191472. A REVIEWK2LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CTM
  191473. 14828
  191474. 2/28/96
  191475. A;RUTHENIUM
  191476. CATALYZED OXIDATIVE TRANSFORMATIONS OF ALCOHOLS. 
  191477. 1994Y
  191478. 13820
  191479. LAROCK, RiCHARD C. 
  191480. Adv. Metal-Org. Chem.C
  191481. A REVIEWK2LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CTM
  191482. 14829N
  191483. 2/28/96
  191484. A*PALLADIUM
  191485. CATALYZED VINYLIC SUBSTITUTION. 
  191486. 1994Y
  191487. 13821
  191488. A_HERNDON, JAMES W.
  191489. TUMER, SENIZ U.
  191490. MCMULLEN, LEONARD A.
  191491. MATASI, JULIUS J.
  191492. SCHNATTER, WAYNE F. K.
  191493. Adv. Metal-Org. Chem.C
  191494. A REVIEWK2LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CTM
  191495. 14830N
  191496. 2/28/96
  191497. AdCYCLOPROPYLCARBENE
  191498. CHROMIUM COMPLEXES: VERSATILE REAGENTS FOR THE SYNTHESIS OF FIVE
  191499. MEMBERED RINGS. 
  191500. 1994Y
  191501. 13822
  191502. A"MAIN, LYNDSAY
  191503. NICHOLSON, BRIAN K. 
  191504. Adv. Metal-Org. Chem.C
  191505. A REVIEWK2LANNY S. LIEBESKIND, ED., JAI PRESS: GREENWICH, CTM
  191506. 14831N
  191507. 2/28/96
  191508. AJORTHO-MANGANATED ARYL KETONES and RELATED COMPOUNDS IN ORGANIC SYNTHESIS .
  191509. 1994Y
  191510. 13823
  191511. A#BAILEY, WILLIAM F.
  191512. OVASKA, TIMO V. 
  191513. Adv. Detailed React. Mech.C
  191514. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191515. 14832N
  191516. 2/28/96
  191517. A:GENERATION and CYCLIZATION OF UNSATURATED ORGANOLITHIUMS. 
  191518. 1994Y
  191519. 13824
  191520. A!BENJES, PAUL A.
  191521. GRIMMETT, M. ROSS
  191522. Adv. Detailed React. Mech.C
  191523. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191524. 14833N
  191525. 2/28/96
  191526. ALKYLATION OF NITROGEN AZOLES.  
  191527. 1994Y
  191528. 13825
  191529. OTERA, JUNZO
  191530. Adv. Detailed React. Mech.C
  191531. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191532. 14834N
  191533. 2/28/96
  191534. A$TEMPLATE EFFECTS OF DISTANNOXANES.  
  191535. 1994Y
  191536. 13826
  191537. A4COXON, JAMES A.
  191538. MCDONALD, D. QUENTIN
  191539. STEEL, PETER J.
  191540. Adv. Detailed React. Mech.C
  191541. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191542. 14835N
  191543. 2/28/96
  191544. A;DIASTEREOFACIAL SELECTIVITY IN THE DIELS
  191545. ALDER REACTION.   
  191546. 1994Y
  191547. 13827
  191548. A'SMITH, ROBIN A. J.
  191549. VELLEKOOP, A. SAMUEL
  191550. Adv. Detailed React. Mech.C
  191551. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191552. 14836N
  191553. 2/28/96
  191554. AH1,4 ADDITION REACTIONS OF ORGANOCUPRATES WITH A,B
  191555. UNSATURATED KETONES.  
  191556. 1994Y
  191557. 13828
  191558. MIKAMI, KOICHI
  191559. SHIMIZU, MASAKI
  191560. Adv. Detailed React. Mech.C
  191561. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191562. 14837N
  191563. 2/28/96
  191564. ARSTEREOELECTRONIC RULES IN ADDITION REACTIONS: "CRAM'S RULE" IN OLEFINIC SYSTEMS.  
  191565. 1994Y
  191566. 13829
  191567. A YAMAMOTO, YOSHINORI
  191568. SHIDA, NAOMI
  191569. Adv. Detailed React. Mech.C
  191570. A REVIEWK-JAMES M. COXON, ED., JAI PRESS: GREENWICH, CTM
  191571. 14838N
  191572. 2/28/96
  191573. ANSTEREOCHEMISTRY and MECHANISM OF ALLYLIC TIN
  191574. ALDEHYDE CONDENSATION REACTIONS. 
  191575. 1994Y
  191576. 13830
  191577. A$MEMMESHEIMER, HOLGER
  191578. REGITZ, MANFRED
  191579. Adv. Carbene Chem.C     A REVIEWK-UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CTM
  191580. 14839N
  191581. 2/28/96
  191582. ADTHE ROLE OF CARBENES IN THE CHEMISTRY OF LOW
  191583. COORDINATED PHOSPHORUS.
  191584. 1994Y
  191585. 13831
  191586. JONES, MAITLAND, JR. 
  191587. Adv. Carbene Chem.C
  191588. A REVIEWK-UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CTM
  191589. 14840N
  191590. 2/28/96
  191591. CARBENES and CARBORANES. 
  191592. 1994Y
  191593. 13832
  191594. A$JACKSON, JAMES E.
  191595. PLATZ, MATTHEW S. 
  191596. Adv. Carbene Chem.C
  191597. A REVIEWK-UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CTM
  191598. 14841N
  191599. 2/28/96
  191600. AGLASER FLASH PHOTOLYSIS STUDIES OF YLIDE
  191601. FORMING REACTIONS OF CARBENES. 
  191602. 1994Y
  191603. 13833
  191604. MOSS, ROBERT A. 
  191605. Adv. Carbene Chem.C
  191606. A REVIEWK-UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CTM
  191607. 14842N
  191608. 2/28/96
  191609. A=ABSOLUTE KINETICS OF INTRAMOLECULAR ALKLYCARBENE REACTIONS.  
  191610. 1994Y
  191611. 13834
  191612. KIRMSE, WOLFGANG
  191613. Adv. Carbene Chem.C
  191614. A REVIEWK-UDO H. BRINKER, ED., JAI PRESS: GREENWICH, CTM
  191615. 14843N
  191616. 2/28/96
  191617. CARBENES and THE O
  191618. H BOND. 
  191619. 1994Y
  191620. 13835
  191621. A/BURES, MARK G.
  191622. MARTIN, YVONNE C.
  191623. WILLETT, PETER
  191624. Topics in Stereochem.C
  191625. A REVIEWM
  191626. 14844N
  191627. 2/28/96
  191628. AMSEARCHING TECHNIQUES FOR DATABASES OF THREE DIMENSIONAL CHEMICAL STRUCTURES. 
  191629. 1994X
  191630. 467-511Y
  191631. 13836
  191632. YOUNG, DOUGLAS W. 
  191633. Topics in Stereochem.C
  191634. A REVIEWM
  191635. 14845N
  191636. 2/28/96
  191637. A7STEREOCHEMISTRY OF METABOLIC REACTIONS OF AMINO ACIDS. 
  191638. 1994X
  191639. 381-465Y
  191640. 13837
  191641. DODZIUK, HELENA
  191642. Topics in Stereochem.C
  191643. A REVIEWM
  191644. 14846N
  191645. 2/28/96
  191646. AYUNUSUAL SATURATED HYDROCARBONS: INTERACTION BETWEEN THEORETICAL and SYNTHETIC CHEMISTRY. 
  191647. 1994X
  191648. 351-380Y
  191649. 13838
  191650. A%GRACZYK, PIOTR P.
  191651. MIKOLAJCZYK, MARIAN
  191652. Topics in Stereochem.C
  191653. A REVIEWM
  191654. 14847N
  191655. 2/28/96
  191656. A*ANOMERIC EFFECT: ORIGIN and CONSEQUENCES. 
  191657. 1994X
  191658. 159-349Y
  191659. 13839
  191660. VEDEJS, E.
  191661. PETERSON, M. J.
  191662. Topics in Stereochem.C
  191663. A REVIEWM
  191664. 14848N
  191665. 2/28/96
  191666. A6STEREOCHEMISTRY and MECHANISM IN THE WITTIG REACTION. 
  191667. 1994X
  191668. 1-157Y
  191669. 13840
  191670. FOOTE, CHRISTOPHER S. 
  191671. Topics Curr. Chem.C
  191672. (ELECTRON TRANSFER I)
  191673. A REVIEWM
  191674. 14849N
  191675. 2/28/96
  191676. A:PHOTOPHYSICAL and PHOTOCHEMICAL PROPERTIES OF FULLERENES. 
  191677. 1994X
  191678. 13841
  191679. MIZUNO, KAZUHIKO
  191680. OTSUJI, YOSHIO
  191681. Topics Curr. Chem.C
  191682. (ELECTRON TRANSFER I),
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  191684. 14850N
  191685. 2/28/96
  191686. AIADDITION and CYCLOADDITION REACTIONS VIA PHOTOINDUCED ELECTRON TRANSFER. 
  191687. 1994X
  191688. 13842
  191689. RETTIG, WOLFGANG
  191690. Topics Curr. Chem.C
  191691. (ELECTRON TRANSFER I)
  191692. A REVIEWM
  191693. 14851N
  191694. 2/28/96
  191695. ASPHOTOINDUCED CHARGE SEPARATION VIA TWISTED INTRAMOLECULAR CHARGE TRANSFER STATES.  
  191696. 1994X
  191697. 13843
  191698. KAIM, WOLFGANG
  191699. Topics Curr. Chem.C
  191700. (ELECTRON TRANSFER I)
  191701.  A REVIEWM
  191702. 14852N
  191703. 2/28/96
  191704. AhTHERMAL and LIGHT INDUCED ELECTRON TRANSFER REACTIONS OF MAIN GROUP METAL HYDRIDES and ORGANOMETALLICS. 
  191705. 1994X
  191706. 13844
  191707. SCHMITTEL, MICHAEL
  191708. Topics Curr. Chem.C
  191709. (ELECTRON TRANSFER I)
  191710.  A REVIEWM
  191711. 14853N
  191712. 2/28/96
  191713. A.UMPOLUNG OF KETONES VIA ENOL RADICAL CATIONS. 
  191714. 1994X
  191715. 13845
  191716. MEMMING, RUDIGER
  191717. Topics Curr. Chem.C
  191718. (ELECTRON TRANSFER I)
  191719.  A REVIEWM
  191720. 14854N
  191721. 2/28/96
  191722. ARPHOTOINDUCED CHARGE TRANSFER PROCESSES AT SEMICONDUCTOR ELECTRODES and PARTICLES. 
  191723. 1994X
  191724. 13846
  191725. A$BAUMGARTEN, MARTIN, F.
  191726. MULLEN, KLAUS
  191727. Topics Curr. Chem.C
  191728. (ELECTRON TRANSFER I)
  191729.  A REVIEWM
  191730. 14855N
  191731. 2/28/96
  191732. A@RADICAL IONS: WHERE ORGANIC CHEMISTRY MEETS MATERIALS SCIENCES. 
  191733. 1994X
  191734. 13847
  191735. BISSELL, RICHARD A.
  191736. DESILVA, A. PRASANNA
  191737. GUNARATNE, H. Q. NIMAL
  191738. LYNCH, P. L. MARK
  191739. MAGUIRE, GLENN E. M.
  191740. MCCOY, COLIN P.
  191741. SANDANAYAKE, K. R. A. SAMANKUMARA. 
  191742. Topics Curr. Chem.C+(PHOTOINDUCED ELECTRON TRANSFER V)
  191743. A REVIEWM
  191744. 14856
  191745. 2/28/96
  191746. A:FLUORESCENT PET (PHOTOINDUCED ELECTRON TRANSFER) SENSORS. 
  191747. 1993X
  191748. 13848
  191749. PANDEY, GANESH
  191750. Topics Curr. Chem.C+(PHOTOINDUCED ELECTRON TRANSFER V)
  191751. A REVIEWM
  191752. 14857N
  191753. 2/28/96
  191754. A;PHOTOINDUCED ELECTRON TRANSFER (PET) IN ORGANIC SYNTHESIS. 
  191755. 1993X
  191756. 13849
  191757. A-ALBINI, ANGE LO
  191758. FASANI, ELISA
  191759. MELLA, MARIELLA
  191760. Topics Curr. Chem.C,(PHOTO INDUCED ELECTRON TRANSFER V)
  191761. A REVIEWM
  191762. 14858N
  191763. 2/28/96
  191764. A&PET
  191765. REACTIONS OF AROMATIC COMPOUNDS.  
  191766. 1993X
  191767. 13850
  191768. SOUMILLION, JEAN
  191769. PHILIPPE
  191770. Topics Curr. Chem.C+(PHOTOINDUCED ELECTRON TRANSFER V)
  191771. A REVIEWM
  191772. 14859N
  191773. 2/28/96V9PHOTOINDUCED ELECTRON TRANSFER EMPLOYING ORGANIC ANIONS. W
  191774. 1993X
  191775. 13851
  191776. A%FREEMAN, PETER K.
  191777. HATLEVIG, SUSAN A. 
  191778. Topics Curr. Chem.C.(PHOTOINDUCED ELECTRON TRANSFER V)  
  191779.  A REVIEWM
  191780. 14860N
  191781. 2/28/96
  191782. THE PHOTOCHEMISTRY OF POLYHALOCOMPOUNDS, DEHALOGENATION BY PHOTO INDUCED ELECTRON TRANSFER, NEW METHODS OF TOXIC WASTE DISPOSAL. 
  191783. 1993X
  191784. 13852
  191785. MASLAK, PRZEMYSLAW 
  191786. Topics Curr. Chem.C+A REVIEW (PHOTOINDUCED ELECTRON TRANSFER V)M
  191787. 14861N
  191788. 2/28/96
  191789. AVFRAGMENTATIONS BY PHOTOINDUCED ELECTRON TRANSFER. FUNDAMENTALS and PRACTICAL ASPECTS. 
  191790. 1993X
  191791. 13853
  191792. GANT, THOMAS G.
  191793. MEYERS, A. I.
  191794. TetrahedronC
  191795. A REVIEWM
  191796. 14862N
  191797. 2/28/96
  191798. A.THE CHEMISTRY OF 2
  191799. OXAZOLINES (1985
  191800. PRESENT). 
  191801. 1994X
  191802. 2297-360Y
  191803. 13854
  191804. DUTHALER, RUDOLF O.
  191805. TetrahedronC
  191806. A REVIEWM
  191807. 14863N
  191808. 2/28/96
  191809. AHRECENT DEVELOPMENTS IN THE STEREOSELECTIVE SYNTHESIS OF A
  191810. AMINO ACIDS.  
  191811. 1994X
  191812. 1539-660Y
  191813. 13855
  191814. MAGNUS, PHILIP
  191815. TetrahedronC
  191816. A REVIEWM
  191817. 14864N
  191818. 2/28/96
  191819. A GENERAL STRATEGY USING N2 CO2(CO)6 ACETYLENE COMPLEXES FOR THE SYNTHESIS OF THE ENEDIYNE ANTITUMOR AGENTS ESPERAMICIN, CALICHEAMICIN, DYNEMICIN and NEOCARZINOSTATIN. 
  191820. 1994X
  191821. 13856
  191822. A.ALBINI, ANGELO
  191823. MELLA, MARIELLA
  191824. FRECCERO, MAURO
  191825. TetrahedronC
  191826. A REVIEWM
  191827. 14865N
  191828. 2/28/96
  191829. A NEW METHOD IN RADICAL CHEMISTRY: GENERATION OF RADICALS BY PHOTO
  191830. INDUCED ELECTRON TRANSFER and FRAGMENTATION OF THE RADICAL CATION.
  191831. 1994X
  191832. 575-607Y
  191833. 13857
  191834. DIAS, JERRY RAY
  191835. TetrahedronC
  191836. A REVIEWM
  191837. 14866N
  191838. 2/28/96
  191839. AsDECIPHERING THE INFORMATION CONTENT OF POLYCYCLIC CONJUGATED HYDROCARBON FORMULAS 
  191840.  FROM BENZENOIDS to FULLERENES. 
  191841. 1993X
  191842. 9207-20Y
  191843. 13858
  191844. A6OSTERHOUT, MARTIN, H.
  191845. NADLER, WILLIAM R.
  191846. PADWA, ALBERT
  191847. B    SynthesisC
  191848. A REVIEWM
  191849. 14867N
  191850. 2/28/96
  191851. RECENT ADVANCES IN THE CYCLOADDITION CHEMISTRY OF ISOMUNCHNONES and THIOISOMUNCHNONES, AN UNDERUTILIZED CLASS OF MESOIONIC COMPOUNDS.  
  191852. 1994X
  191853. 13859
  191854. A JARAMILLO, CARLOS
  191855. KNAPP, SPENCER
  191856. B    SynthesisC
  191857. A REVIEWM
  191858. 14868N
  191859. 2/28/96
  191860. A!SYNTHESIS OF C
  191861. ARYL GLYCOSIDES.  
  191862. 1994X
  191863. 1-20Z
  191864. 13860
  191865. A$RODRIGUEZ, Jean
  191866. DULCERE, JEAN PIERRE
  191867. B    SynthesisC
  191868. A REVIEWM
  191869. 14869N
  191870. 2/28/96
  191871. A&COHALOGENATION IN ORGANIC SYNTHESIS.  
  191872. 1993X    1177-1205Z
  191873. 13861
  191874. BANFI, LUCA
  191875. GUANTI, GIUSEPPE
  191876. B    SynthesisC
  191877. A REVIEWM
  191878. 14870N
  191879. 2/28/96
  191880. AdASYMMETRIZED 2
  191881. METHYL
  191882. PROPANEDIOL AND ITS EQUIVALENTS: PREPARATION and SYNTHETIC APPLICATIONS.  
  191883. 1993X
  191884. 1029-56Z
  191885. 13862
  191886. KEGLEVICH, GYORGY
  191887. B    SynthesisC
  191888. A REVIEWM
  191889. 14871N
  191890. 2/28/96
  191891. ALSYNTHESIS OF 6
  191892.  and 7
  191893. MEMBERED PHOSPHORUS HETEROCYCLES BY RING ENLARGEMENT. 
  191894. 1993X
  191895. 931-42Z
  191896. 13863
  191897. A>ELNAGDI, MOHAMED HILMY
  191898. NEGM, ABDALLA MOHAMED
  191899. SADEK, KAMAL USEF
  191900. SynlettC
  191901. A REVIEWM
  191902. 14872N
  191903. 2/28/96
  191904. ArALKYLHETEROAROMATICS AS BUILDING BLOCKS FOR THE SYNTHESIS OF CONDENSED POLYFUNCTIONALLY SUBSTITUTED HETEROCYCLES. 
  191905. 1994X
  191906. 27-37Z
  191907. 13864
  191908. SMADJA, WILLIAM
  191909. SynlettC
  191910. A REVIEWM
  191911. 14873N
  191912. 2/28/96
  191913. AfACYCLIC DIASTEREOFACIAL SELECTION IN INTERMOLECULAR RADICAL REACTIONS. STERIC VS. ELECTRONIC CONTROLS.
  191914. 1994X
  191915. 1-25Z
  191916. 13865
  191917. RANU, BRINDABAN C. 
  191918. SynlettC
  191919. A REVIEWM
  191920. 14874N
  191921. 2/28/96
  191922. A:ZINC BOROHYDRIDE 
  191923.  A REDUCING AGENT WITH HIGH POTENTIAL.  
  191924. 1993X
  191925. 885-92Z
  191926. 13866
  191927. ARSONAWANE, HARIKISAN R.
  191928. BELLUR, NANJUNDIAH S.
  191929. KULKARNI, DILIP G.
  191930. AHUJA, JAIMALA R. 
  191931. SynlettC
  191932. A REVIEWM
  191933. 14875N
  191934. 2/28/96
  191935. PHOTOINDUCED VINYLCYCLOPROPANE
  191936. CYCLOPENTENE REARRANGEMENT (PHOTO
  191937. CP): A METHODOLOGY FOR CHIRAL BICYCLO[3.2.0]HEPTENES and THEIR APPLICATION IN NATURAL PRODUCT SYNTHESES. 
  191938. 1993X
  191939. 13867
  191940. KAHN, MICHAEL
  191941. SynlettC
  191942. A REVIEWM
  191943. 14876N
  191944. 2/28/96
  191945. AMPEPTIDE SECONDARY STRUCTURE MIMETICS: RECENT ADVANCES and FUTURE CHALLENGES. 
  191946. 1993X
  191947. 821-6Z
  191948. 13868
  191949. NORTH, MICHAEL
  191950. SynlettC
  191951. A REVIEWM
  191952. 14877N
  191953. 2/28/96V,CATALYTIC ASYMMETRIC CYANOHYDRIN SYNTHESIS. W
  191954. 1993X
  191955. 807-20Z
  191956. 13869
  191957. A,ASFARI, ZOUHAIR
  191958. WEISS,  Jean
  191959. VICENS, JACQUES
  191960. SynlettC
  191961. A REVIEWM
  191962. 14878N
  191963. 2/28/96
  191964. A5DOUBLE
  191965. CALIXARENE DESIGN, SYNTHESIS, and PROPERTIES. 
  191966. 1993X
  191967. 719-25Z
  191968. 13870
  191969. ARZEFIROV, NIKOLAI S.
  191970. ZYK, NIKOLAI V.
  191971. BELOGLAZKINA, ELENA K.
  191972. KUTATELADZE, ANDREI G. 
  191973. Sulfur ReportsC
  191974. A REVIEWM
  191975. 14879N
  191976. 2/28/96
  191977. AATHIOSULFONATES: SYNTHESIS, REACTIONS and PRACTICAL APPLICATIONS. 
  191978. 1993X
  191979. 223-40Y
  191980. 13871
  191981. KOVAL, IVAN V. 
  191982. Sulfur ReportsC
  191983. A REVIEWM
  191984. 14880N
  191985. 2/28/96
  191986. A?ADVANCES IN THE CHEMISTRY OF SULFIMIDES and RELATED COMPOUNDS. 
  191987. 1993X
  191988. 149-215Y
  191989. 13872
  191990. A TAKAHASHI, MASAKI
  191991. OKAZAKI, RENJI
  191992. Sulfur ReportsC
  191993. A REVIEWM
  191994. 14881N
  191995. 2/28/96
  191996. A(THE CHEMISTRY OF THIONITROSO COMPOUNDS. 
  191997. 1993X
  191998. 293-341Y
  191999. 13873
  192000. A-MITCHELL, S. C.
  192001. NICKSON, R. M.
  192002. WARING, R. H. 
  192003. Sulfur ReportsC
  192004. A REVIEWM
  192005. 14882N
  192006. 2/28/96
  192007. A-THE BIOLOGICAL ACTIVITY OF SELENIUM SULFIDE. 
  192008. 1993X
  192009. 279-92Y
  192010. 13874
  192011. FIELD, LAMAR
  192012. Sulfur ReportsC
  192013. A REVIEWM
  192014. 14883N
  192015. 2/28/96
  192016. A6FORTY
  192017. FIVE YEARS WITH A HYDRA, ORGANOSULFUR CHEMISTRY.
  192018. 1993X
  192019. 197-277Y
  192020. 13875
  192021. MITCHELL, S. C.
  192022. NICKSON, R. M. 
  192023. Sulfur ReportsC
  192024. A REVIEWM
  192025. 14884N
  192026. 2/28/96
  192027. A-METABOLISM OF SULFUR
  192028. CONTAINING XENOBIOTICS. 
  192029. 1993X
  192030. 161-85Y
  192031. 13876
  192032. A2DERYAGINA, E. N.
  192033. VORONKOV, M. G.
  192034. KORCHEVIN, N. A. 
  192035. Russ. Chem. Rev.C
  192036. A REVIEWM
  192037. 14885N
  192038. 2/28/96
  192039. A+SELENIUM
  192040.  and TELLURIUM
  192041. CENTeRED RADICALS. 
  192042. 1993X
  192043. 1107Y
  192044. 13877
  192045. ESIPENKO, A. A.
  192046. SAMARAI, L. I. 
  192047. Russ. Chem. Rev.C
  192048. A REVIEWM
  192049. 14886N
  192050. 2/28/96
  192051. AKCYCLOADDITION OF NITRILE OXIDES to MULTIPLE BONDS CONTAINING A HETEROATOM. 
  192052. 1993X
  192053. 1097Y
  192054. 13878
  192055. USOV, A. I. 
  192056. Russ. Chem. Rev.C
  192057. A REVIEWM
  192058. 14887N
  192059. 2/28/96
  192060. A)OLIGOSACCHARINS 
  192061.  A NEW CLASS OF SIGNAL. 
  192062. 13879
  192063. GINZBURG, A. G. 
  192064. Russ. Chem. Rev.C
  192065. A REVIEWM
  192066. 14888N
  192067. 2/28/96
  192068. THE CHEMISTRY OF CYMANTRENE.
  192069. 1993X
  192070. 1025Y
  192071. 13880
  192072. A/SOKOLYUK, N. T.
  192073. ROMANOV, V. V.
  192074. PISULINA, L. P. 
  192075. Russ. Chem. Rev.C
  192076. A REVIEWM
  192077. 14889N
  192078. 2/28/96
  192079. A/NAPHTHACENEQUINONES: SYNTHESIS and PROPERTIES. 
  192080. 1993X
  192081. 1005Y
  192082. 13881
  192083. A5KARTASHOV, V. R.
  192084. SKOROBOGATOVA, E. V.
  192085. ZEFIROV, N. S. 
  192086. Russ. Chem. Rev.C
  192087. A REVIEWM
  192088. 14890N
  192089. 2/28/96
  192090. A:REACTIONS OF CYCLOPROPENE DERIVATIVES WITH ELECTROPHILES. 
  192091. 1993X
  192092. 13882
  192093. A2BRODSKAYA, E. I.
  192094. RATOVSKII, G. V.
  192095. VORONKOV, M. G. 
  192096. Russ. Chem. Rev.C
  192097. A REVIEWM
  192098. 14891N
  192099. 2/28/96
  192100. A7ORBITAL INTERACTION THROUGH SPACE and THROUGH O
  192101. BONDS. 
  192102. 1993X
  192103. 13883
  192104. AVOTINS, F. 
  192105. Russ. Chem. Rev.C
  192106. A REVIEWM
  192107. 14892N
  192108. 2/28/96
  192109. A&AMINOACIDS OF THE CYCLOBUTANE SERIES. 
  192110. 1993X
  192111. 13884
  192112. AwDORFMAN, YA. A.
  192113. ALESHKOVA, M. M.
  192114. POLIMBETOVA, G. S.
  192115. LEVINA, L. V.
  192116. PETROVA, T. V.
  192117. ABDREIMOVA, R. R.
  192118. DOROSHKEVICH, D. M. 
  192119. Russ. Chem. Rev.C
  192120. A REVIEWM
  192121. 14893N
  192122. 2/28/96
  192123. NEW REACTIONS INVOLVING THE OXIDATIVE O
  192124. , AND C
  192125. PHOSPHORYLATION OF ORGANIC COMPOUNDS BY PHOSPHORUS and PHOSPHIDES IN THE PRESENCE OF METAL COMPLEXES.
  192126. 1993X
  192127. 13885
  192128. KULINKOVICH, O. G.
  192129. Russ. Chem. Rev.
  192130. A REVIEWM
  192131. 14894N
  192132. 2/28/96
  192133. AXACTIVATED CYCLOPROPANES IN THE SYNTHESIS OF FIVE
  192134. MEMBERED CARBOCYCLES and HETEROCYCLES. 
  192135. 1993X
  192136. 13886
  192137. A@TOMILOV, YU. V.
  192138. DOKICHEV, V. A.
  192139. DZHEMILEV, U. M.
  192140. NEFEDOV, O. M. 
  192141. Russ. Chem. Rev.C
  192142. A REVIEWM
  192143. 14895N
  192144. 2/28/96
  192145. AiCATALYTIC DECOMPOSITION OF DIAZOMETHANE AS A GENERAL METHOD FOR THE METHYLENATION OF CHEMICAL COMPOUNDS. 
  192146. 1993X
  192147. 13887
  192148. VOLKOV, S. K. 
  192149. Russ. Chem. Rev.C
  192150. A REVIEWM
  192151. 14896N
  192152. 2/28/96
  192153. IMMUNOASSAY OF ALKALOIDS. 
  192154. 1993X
  192155. 13888
  192156. KOVAL, I. V. 
  192157. Russ. Chem. Rev.C
  192158. A REVIEWM
  192159. 14897N
  192160. 2/28/96
  192161. THIOLS AS SYNTHONS. 
  192162. 1993X
  192163. 13889
  192164. KEIKO, N. A.
  192165. VORONKOV, M. G. 
  192166. Russ. Chem. Rev.C
  192167. A REVIEWM
  192168. 14898N
  192169. 2/28/96
  192170. ACMETHODS OF SYNTHESIS OF ACROLEIN and ITS A
  192171. SUBSTITUTED DERIVATIVES.
  192172. 1993X
  192173. 13890
  192174. A)AMABILINO, DAVID B.
  192175. STODDART, J. FRASER. 
  192176. Pure App. Chem.C
  192177. A REVIEWM
  192178. 14899N
  192179. 2/28/96
  192180. A)SELF ASSEMBLY and MACROMOLECULAR DESIGN. 
  192181. 1993X
  192182. 2351-9Y
  192183. 13891
  192184. A]BRODESSER, G.
  192185. CUETHER, R.
  192186. HOSS, R.; MEIER, S.
  192187. OTTENS, HILDEBRANDT S.
  192188. SCHMITZ, J.
  192189. VOEGTLE, F. 
  192190. Pure App. Chem.C
  192191. A REVIEWM
  192192. 14900N
  192193. 2/28/96
  192194. ACNEW TAILORED HOSTS: FROM MOLECULAR RECOGNITION to MECHANICAL BONDS.
  192195. 1993X
  192196. 2325-8Y
  192197. 13892
  192198. A?MURAKAMI, YUKITO
  192199. HAYASHIDA, OSAMU
  192200. Ono, KAZUYA
  192201. HISAEDA, YOSHIO. 
  192202. Pure App. Chem.C
  192203. A REVIEWM
  192204. 14901N
  192205. 2/28/96
  192206. THERMODYNAMICAL and GEOMETRICAL CHARACTERIZATION OF MOLECULAR RECOGNITION BY CAGE
  192207. TYPE and PEPTIDE AZAPARACYCLOPHANES IN AQUEOUS MEDIA. 
  192208. 1993X
  192209. 13893
  192210. AjANDREU, CECILIA
  192211. BEERLI, RENE
  192212. BRANDA, NEIL
  192213. CONN, MORGAN
  192214. DE, MENDOZA JAVIER
  192215. GALAN, AMALIA
  192216. HUC, IVAN, ET AL. 
  192217. Pure App. Chem.C
  192218. A REVIEWM
  192219. 14902N
  192220. 2/28/96
  192221. REPLICATION and ASSEMBLY. 
  192222. 1993X
  192223. 2313-18Y
  192224. 13894
  192225. BELOV, YURI P. 
  192226. Pure App. Chem.C
  192227. A REVIEWM
  192228. 14903N
  192229. 2/28/96
  192230. AqCHIRAL MOBILE PHASES IN THE ENANTIOMERIC ANALYSIS and IN THE EVALUATION OF STABILITY CONSTANTS OF p
  192231. p COMPLEXES. 
  192232. 1993X
  192233. 2273-80Y
  192234. 13895
  192235. A)ENGEWALD, W.
  192236. REINHARDT, R.
  192237. STEINBORN, A. 
  192238. Pure App. Chem.C
  192239. A REVIEWM
  192240. 14904N
  192241. 2/28/96
  192242. AQTHE USE OF SHAPE
  192243. SELECTIVE STATIONARY PHASES IN GC. PART 1: CYCLODEXTRIN PHASES. 
  192244. 1993X
  192245. 2253-6Y
  192246. 13896
  192247. A'LETARD, J. F.
  192248. LAPOUYADE, R.
  192249. RETTIG, W. 
  192250. Pure App. Chem.C
  192251. A REVIEWM
  192252. 14905N
  192253. 2/28/96
  192254. SYNTHESIS AND PHOTOPHYSICAL STUDY OF 4
  192255. MONOAZA
  192256. CROWN
  192257. 5)STILBENES FORMING TWISTED INTRAMOLECULAR CHARGE TRANSFER STATES and THEIR COMPLEXATION WITH CATIONS. 
  192258. 1993X
  192259. 13897
  192260. A/SZAJDZINSKA, PIETEK E.
  192261. GEBICKI, J. L.
  192262. KROH, J. 
  192263. Pure App. Chem.C
  192264. A REVIEWM
  192265. 14906N
  192266. 2/28/96
  192267. AUSCAVENGING OF HYDRATED ELECTRONS BY HYDROPHOBIC SOLUTES IN IONIC MICELLAR SOLUTIONS. 
  192268. 1993X
  192269. 1617-23Y
  192270. 13898
  192271. A7ZHU, QI CONG
  192272. HUTCHINS, ROBERT O.
  192273. HUTCHINS, MARYGAIL K. 
  192274. Org. Prep. Proc. Int.C
  192275. A REVIEWM
  192276. 14907N
  192277. 2/28/96
  192278. A7ASYMMETRIC REDUCTIONS OF CARBON
  192279. NITROGEN DOUBLE BONDS. 
  192280. 1994X
  192281. 193-236Y
  192282. 13899
  192283. A#KOTALI, ANTIGONI
  192284. HARRIS, PHILIP A. 
  192285. Org. Prep. Proc. Int.C
  192286. A REVIEWM
  192287. 14908N
  192288. 2/28/96
  192289. HYDROXYARYL KETONES IN ORGANIC SYNTHESIS.  
  192290. 1994X
  192291. 159-92Y
  192292. 13900
  192293. Oh, TAEBOEM
  192294. REILLY, MICHAEL
  192295. Org. Prep. Proc. Int.C
  192296. A REVIEWM
  192297. 14909N
  192298. 2/28/96
  192299. A5REAGENT
  192300. CONTROLLED ASYMMETRIC DIELS
  192301. ALDER REACTIONS. 
  192302. 1994X
  192303. 129-58Y
  192304. 13901
  192305. SHIBATA, IKUYA
  192306. Baba, Akio
  192307. Org. Prep. Proc. Int.C
  192308. A REVIEWM
  192309. 14910N
  192310. 2/28/96
  192311. A)ORGANOTIN ENOLATES IN ORGANIC SYNTHESIS. 
  192312. 1994X
  192313. 85-100Y
  192314. 13902
  192315. A7ALLEN, ANGELA J.
  192316. VAILLANCOURT, VALERIE
  192317. ALBIZATI, Kim F.
  192318. Org. Prep. Proc. Int.C
  192319. A REVIEWM
  192320. 14911N
  192321. 2/28/96V
  192322. FURANOSESQUITERPENE SYNTHESIS. W
  192323. 1994X
  192324. 1-84Y
  192325. 13903
  192326. HUGHES, DAVID L.
  192327. Org. Prep. Proc. Int.C
  192328. A REVIEWM
  192329. 14912N
  192330. 2/28/96
  192331. A)PROGRESS IN THE FISCHER INDOLE REACTION. 
  192332. 1993X
  192333. 607-32Y
  192334. 13904
  192335. A'NATALE, NICHOLAS R.
  192336. MIRZAEI, YOUSEF R. 
  192337. Org. Prep. Proc. Int.C
  192338. A REVIEWM
  192339. 14913N
  192340. 2/28/96
  192341. A&THE LATERAL METALATION OF ISOXAZOLES. 
  192342. 1993X
  192343. 515-56Y
  192344. 13905
  192345. KARP, GARY M. 
  192346. Org. Prep. Proc. Int.C
  192347. A REVIEWM
  192348. 14914N
  192349. 2/28/96
  192350. A1PREPARATION and REACTIONS OF INDOLIN
  192351. 2(3H)
  192352. ONES. 
  192353. 1993X
  192354. 481-513Y
  192355. 13906
  192356. A.CLAUSEN, FINN PRIESS
  192357. Juhl, CHRISTENSEN JOERGEN
  192358. Org. Prep. Proc. Int.C
  192359. A REVIEWM
  192360. 14915N
  192361. 2/28/96
  192362. A%SYNTHESIS OF 9
  192363. SUBSTITUTED GUANINES. 
  192364. 1993X
  192365. 375-401Y
  192366. 13907
  192367. O'HAGAN, D. 
  192368. Nat. Prod. Rep.C
  192369. A REVIEWM
  192370. 14916N
  192371. 2/28/96
  192372. A7BIOSYNTHESIS OF FATTY ACID and POLYKETIDE METABOLITES. 
  192373. 1993X
  192374. 593-624Y
  192375. 13908
  192376. HERBERT, R. B. 
  192377. Nat. Prod. Rep.C
  192378. A REVIEWM
  192379. 14917N
  192380. 2/28/96
  192381. AKTHE BIOSYNTHESIS OF PLANT ALKALOIDS and NITROGENOUS MICROBIAL METABOLITES. 
  192382. 1993X
  192383. 575-92Y
  192384. 13909
  192385. MURPHY, J. A.
  192386. GRIFfLTHS, J. 
  192387. Nat. Prod. Rep.C
  192388. A REVIEWM
  192389. 14918N
  192390. 2/28/96
  192391. APA SURVEY OF NATURAL PRODUCTS WHICH ABSTRACT HYDROGEN ATOMS FROM NUCLEIC ACIDS.  
  192392. 1993X
  192393. 551-64Y
  192394. 13910
  192395. ENDO, A.
  192396. HASUMI, K 
  192397. Nat. Prod. Rep.C
  192398. A REVIEWM
  192399. 14919N
  192400. 2/28/96
  192401. COA REDUCTASE INHIBITORS. 
  192402. 1993X
  192403. 541-50Y
  192404. 13911
  192405. MODERHACK, DIETRICH
  192406. J. Het. Chem.C
  192407. A REVIEWM
  192408. 14920N
  192409. 2/28/96
  192410. A=OXO
  192411.  and IMINO
  192412. FUNCTIONALIZED 1,2
  192413. OXAZETIDINES. AN OVERVIEW. 
  192414. 1993X
  192415. 13912
  192416. A CATSOULACOS, P.
  192417. CATSOULACOS, D. 
  192418. J. Het. Chem.C
  192419. A REVIEWM
  192420. 14921N
  192421. 2/28/96
  192422. FORMATION OF HOMO
  192423. STEROIDS and DERIVATIVES BY BECKMANN REARRANGEMENT. ANTITUMOR ACTIVITY OF STEREOISOMERS HOMOAZA
  192424. STEROIDAL ESTERS. 
  192425. 1993X
  192426. 1-10Y
  192427. 13913
  192428. A%DEGA, SZAFRAN ZOFIA
  192429. SZAFRAN, MIROSLAW
  192430. HeterocyclesC
  192431. A REVIEWM
  192432. 14922N
  192433. 2/28/96
  192434. ADCOMPLEXES OF CARBOXYLIC ACIDS WITH PYRIDINES and PYRIDINE N
  192435. OXIDES. 
  192436. 1994X
  192437. 627-59Y
  192438. 13914
  192439. PIOZZI, FRANCO
  192440. HeterocyclesC
  192441. A REVIEWM
  192442. 14923N
  192443. 2/28/96
  192444. AAFURTHER RESEARCHES ON THE FUROCLE RODANES FROM TEUCRIUM SPECIES. 
  192445. 1994X
  192446. 603-26Y
  192447. 13915
  192448. A%MORENO, MANAS MARCIAL
  192449. PLEIXATS, ROSER
  192450. HeterocyclesC
  192451. A REVIEWM
  192452. 14924N
  192453. 2/28/96
  192454. AZBICYCLIC COMPOUNDS STRUCTURALLY RELATED to DEHYDROACETIC ACID and TRIACETIC ACID LACTONE. 
  192455. 1994X
  192456. 585-601Y
  192457. 13916
  192458. A#BUTLER, RICHARD N.
  192459. OSHEA, DONAL F. 
  192460. HeterocyclesC
  192461. A REVIEWM
  192462. 14925N
  192463. 2/28/96
  192464. ApSUBSTITUTED 1,2,3
  192465. TRIAZOLIUM
  192466. YLIDES AS 1,3
  192467. DIPOLES: SYNTHONS FOR A RANGE OF AZIMINE and 1,2,3
  192468. TRIAZA SYSTEMS. 
  192469. 1994X
  192470. 571-84Y
  192471. 13917
  192472. PELTER, ANDREW
  192473. WARD, ROBERT S. 
  192474. HeterocyclesC
  192475. A REVIEWM
  192476. 14926N
  192477. 2/28/96
  192478. A?REACTIONS OF 2,6-DIARYL
  192479. DIOXABICYCLO[3.3.0]OCTANE LIGNANS. 
  192480. 1994X
  192481. 137-47Y
  192482. 13918
  192483. KATRITZKY, Alan R.
  192484. HeterocyclesC
  192485. A REVIEWM
  192486. 14927N
  192487. 2/28/96
  192488. AESUMMARY OF KATRITZKY RESEARCH GROUP SCIENTIFIC RESULTS (1954
  192489. 1993).  
  192490. 1994X
  192491. 3-130Y
  192492. 13919
  192493. A;PRICE, WILLIAM A.
  192494. SILVA, ARTUR M. S.
  192495. CAVALEIRO, JOSE A. S. 
  192496. HeterocyclesC
  192497. A REVIEWM
  192498. 14928N
  192499. 2/28/96
  192500. STYRYLCHROMONES: BIOLOGICAL ACTION, SYNTHESIS and REACTIVITY. 
  192501. 1993X
  192502. 2601-11Y
  192503. 13920
  192504. A0SLIWA, WANDA
  192505. CHRZASTEK, LIDIA
  192506. MIELNICZAK, MARIAN
  192507. HeterocyclesC
  192508. A REVIEWM
  192509. 14929N
  192510. 2/28/96
  192511. A6HOST
  192512. GUEST COMPLEXES OF AZAAROMATIC QUATERNARY SALTS. 
  192513. 1993X
  192514. 1645-78Y
  192515. 13921
  192516. A,HADDADIN. MAKHLUF J.
  192517. ISSIDORIDES, COSTAS H. 
  192518. HeterocyclesC
  192519. A REVIEWM
  192520. 14930N
  192521. 2/28/96V
  192522. THE BEIRUT REACTION.  W
  192523. 1993X
  192524. 1503-25Y
  192525. 13922
  192526. HASSNER, ALFRED
  192527. FISCHER, BILHA
  192528. HeterocyclesC
  192529. A REVIEWM
  192530. 14931N
  192531. 2/28/96
  192532. NEW CHEMISTRY OF OXAZOLES. 
  192533. 1993X
  192534. 1441-65Y
  192535. 13923
  192536. MURRAY, WILLIAM V. 
  192537. Chemtracts: Org. Chem.C
  192538. A REVIEWM
  192539. 14932N
  192540. 2/28/96
  192541. AaANGIOTENSIN II RECEPTOR ANTAGONISTS: THE NEXT STEP IN THE EVOLUTION OF ANTIHYPERTENSIVE THERAPY. 
  192542. 1994X
  192543. 263-284Y
  192544. 13924
  192545. LOWN, J. WILLIAM
  192546. Chemtracts: Org. Chem.C
  192547. A REVIEWM
  192548. 14933N
  192549. 2/28/96
  192550. AiTARGETING THE DNA MINOR GROOVE FOR CONTROL OF BIOLOGICAL FUNCTION: PROGRESS, CHALLENGES, and PROSPECTS.  
  192551. 1994X
  192552. 205-237Y
  192553. 13925
  192554. THIBBLIN, ALF
  192555. Chem. Soc. Rev.C
  192556. A REVIEWM
  192557. 14934N
  192558. 2/28/96
  192559. A?MECHANISMS OF SOLVOLYTIC ALKENE FORMING ELIMINATION REACTIONS. 
  192560. 1993X
  192561. 427-33Y
  192562. 13926
  192563. MARCUS, Y. 
  192564. Chem. Soc. Rev.C
  192565. A REVIEWM
  192566. 14935N
  192567. 2/28/96
  192568. AXTHE PROPERTIES OF ORGANIC LIQUIDS THAT ARE RELEVANT to THEIR USE AS SOLVATING SOLVENTS. 
  192569. 1993X
  192570. 409-16Y
  192571. 13927
  192572. A!Webb, THOMAS H.
  192573. WILCOX, CRAIG S. 
  192574. Chem. Soc. Rev.C
  192575. A REVIEWM
  192576. 14936N
  192577. 2/28/96
  192578. ATENANTIOSELECTIVE AND DIASTEREOSELECTIVE MOLECULAR RECOGNITION OF NEUTRAL MOLECULES. 
  192579. 1993X
  192580. 383-95Y
  192581. 13928
  192582. HOLLAS, J. MICHAEL. 
  192583. Chem. Soc. Rev.C
  192584. A REVIEWM
  192585. 14937N
  192586. 2/28/96
  192587. DETERMINATION OF MOLECULAR CONFORMATION FROM LARGE AMPLITUDE VIBRATIONS IN ELECTRONIC SPECTRA OF ORGANIC MOLECULES IN A SUPERSONIC JET. 
  192588. 1993X
  192589. 13929
  192590. PERUTZ, ROBIN N. 
  192591. Chem. Soc. Rev.C
  192592. A REVIEWM
  192593. 14938N
  192594. 2/28/96
  192595. V1ORGANOMETALLIC INTERMEDIATES: ULTIMATE REAGENTS. W
  192596. 1993X
  192597. 361-9Y
  192598. 13930
  192599. A#DAVIS, ANTHONY P. CHOLAPHANESET, AL
  192600. Chem. Soc. Rev.C
  192601. A REVIEWM
  192602. 14939N
  192603. 2/28/96
  192604. A;STEROIDS ASSTRUCTURAL COMPONENTS IN MOLECULAR ENGINEERING. 
  192605. 1993X
  192606. 243-53Y
  192607. 13931
  192608. A-IQBAL, JAVED
  192609. BHATIA, BEENA
  192610. NAYYAR, NARESH K. 
  192611. Chem. Rev.C
  192612. A REVIEWM
  192613. 14940N
  192614. 2/28/96
  192615. AnTRANSITION METAL
  192616. PROMOTED FREE
  192617. RADICAL REACTIONS IN ORGANIC SYNTHESIS: THE FORMATION OF CARBON
  192618. CARBON BONDS.  
  192619. 1994X
  192620. 519-64Y
  192621. 13932
  192622. A$THURSTON, DAVID E.
  192623. BOSE, D. SUBHAS. 
  192624. Chem. Rev.C
  192625. A REVIEWM
  192626. 14941N
  192627. 2/28/96
  192628. AASYNTHESIS OF DNA
  192629. INTERACTIVE PYRROLO[2,1
  192630. C][1,4]BENZODIAZEPINES. 
  192631. 1994X
  192632. 433-65Y
  192633. 13933
  192634. ABKIPLINGER, JAQUELINE L.
  192635. RICHMOND, THOMAS G.
  192636. OSTERBERG, CAROLYN E. 
  192637. Chem. Rev.C
  192638. A REVIEWM
  192639. 14942N
  192640. 2/28/96
  192641. A9ACTIVATION OF CARBON
  192642. FLUORINE BONDS BY METAL COMPLEXES.  
  192643. 1994X
  192644. 373-431Y
  192645. 13934
  192646. A8MONTFORTS, FRANZ PETER
  192647. GERLACH, BENJAMIN
  192648. HOEPER, FRANK. 
  192649. Chem. Rev.C
  192650. A REVIEWM
  192651. 14943N
  192652. 2/28/96
  192653. AADISCOVERY and SYNTHESIS OF LESS COMMON NATURAL HYDROPORPHYRINS.  
  192654. 1994X
  192655. 327-47Y
  192656. 13935
  192657. A%HAIDUC, I.
  192658. KING, R. B.
  192659. NEWTON, M. G. 
  192660. Chem. Rev.C     A REVIEWM
  192661. 14944N
  192662. 2/28/96
  192663. AwSTEREOCHEMICAL ASPECTS OF TELLURIUM COMPLEXES WITH SULFUR LIGANDS: MOLECULAR COMPOUNDS and SUPRAMOLECULAR ASSOCIATIONS.
  192664. 1994X
  192665. 301-26Y
  192666. 13936
  192667. A?VAN VEGGEL, FRANK C. J. M.
  192668. VERBOOM, WILLEM
  192669. REINHOUDT, DAVID N. 
  192670. Chem. Rev.C     A REVIEWM
  192671. 14945N
  192672. 2/28/96
  192673. AZMETALLOMACROCYCLES: SUPRAMOLECULAR CHEMISTRY WITH HARD and SOFT METAL CATIONS IN ACTION.  
  192674. 1994X
  192675. 279-99Y
  192676. 13937
  192677. A=BREDAS, J. L.
  192678. ADANT, C.
  192679. TACKX, P.
  192680. PERSOONS, A.
  192681. PIERCE, B. M. 
  192682. Chem. Rev.C
  192683. A REVIEWM
  192684. 14946N
  192685. 2/28/96
  192686. AcTHIRD
  192687. ORDER NONLINEAR OPTICAL RESPONSE IN ORGANIC MATERIALS: THEORETICAL and EXPERIMENTAL ASPECTS. 
  192688. 1994X
  192689. 243-78Y
  192690. 13938
  192691. SCHUBERT, ULRICH
  192692. A REVIEWM
  192693. 14947N
  192694. 2/28/96
  192695. FORMATION and BREAKING SI
  192696. 13939
  192697. Bach, T.
  192698. Angew. Chem. Int. Ed. Engl. C
  192699. A REVIEWM
  192700. 14948N
  192701. 2/28/96
  192702. AUCATALYTIC ENANTIOSELECTIVE C
  192703. C COUPLING ALLYL TRANSFER and MUKAIYAMA ALDOL REACTION. 
  192704. 1994X
  192705. 417-19Y
  192706. 13940
  192707. HOSS, R.
  192708. VOGTLE, F. 
  192709. Angew. Chem. Int. Ed. Engl. C
  192710. A REVIEWM
  192711. 14949N
  192712. 2/28/96V
  192713. TEMPLATE SYNTHESES. W
  192714. 1994X
  192715. 375-84Y
  192716. 13941
  192717. LISKAMP, ROB M. J. 
  192718. Angew. Chem. Int. Ed. Engl. C
  192719. A REVIEWM
  192720. 14950N
  192721. 2/28/96
  192722. AYA NEW APPLICATION OF MODIFIED PEPTIDES and PEPTIDOMIMETICS: POTENTIAL ANTICANCER AGENTS. 
  192723. 1994X
  192724. 305-7Y
  192725. 13942
  192726. SCHMALZ, HANS
  192727. GUNTHER
  192728. Angew. Chem. Int. Ed. Engl. C
  192729. A REVIEWM
  192730. 14951N
  192731. 2/28/96
  192732. AXCHROMIUM CARBENE COMPLEXES IN ORGANIC SYNTHESIS: RECENT DEVELOPMENTS and PERSPECTIVES.  
  192733. 1994X
  192734. 303-5Y
  192735. 13943
  192736. HERGES, RAINER
  192737. Angew. Chem. Int. Ed. Engl. C
  192738. A REVIEWM
  192739. 14952N
  192740. 2/28/96
  192741. AUORGANIZING PRINCIPLE OF COMPLEX REACTIONS and THEORY OF COARCTATE TRANSITION STATES. 
  192742. 1994X
  192743. 255-76Y
  192744. 13944
  192745. AGGARWAL, VARINDER KUMar
  192746. Angew. Chem. Int. Ed. Engl. C
  192747. A REVIEWM
  192748. 14953N
  192749. 2/28/96
  192750. AmENANTIOSELECTIVE TRANSFORMATIONS and RACEMIZATION STUDIES OF HETEROATOM SUBSTITUTED ORGANOLITHIUM COMPOUNDS. 
  192751. 1994X
  192752. 175-7Y
  192753. 13945
  192754. LEITNER, WALTER
  192755. Angew. Chem. Int. Ed. Engl. C
  192756. A REVIEWM
  192757. 14954N
  192758. 2/28/96
  192759. ABA NICKEL COMPLEX FOR PHOTOCHEMICAL ACTIVATION OF CARBON DIOXIDE.  
  192760. 1994X
  192761. 173-4Y
  192762. 13946
  192763. HULLIGER, JUERG
  192764. Angew. Chem. Int. Ed. Engl. C
  192765. A REVIEWM
  192766. 14955N
  192767. 2/28/96
  192768. CHEMISTRY and CRYSTAL GROWTH.  
  192769. 1994X
  192770. 143-62Y
  192771. 13947
  192772. REISER, OLIVIER
  192773. Angew. Chem. Int. Ed. Engl. C
  192774. A REVIEWM
  192775. 14956N
  192776. 2/28/96
  192777. A)OXIDATION OF WEAKLY ACTIVATED C
  192778. H BONDS. 
  192779. 1994X
  192780. 69-72Y
  192781. 13948
  192782. FINK, GEORG
  192783. Angew. Chem. Int. Ed. Engl. C
  192784. A REVIEWM
  192785. 14957N
  192786. 2/28/96
  192787. A{COOPERATIVE EFFECT IN RH2 COMPLEXES: HIGH CATALYTIC ACTIVITY and HIGH REGIOSELECTIVITY IN THE HYDROFORMYLATION OF OLEFINS. 
  192788. 1994X
  192789. 67-9Y
  192790. 13949
  192791. A8NICOLAOU, KYRIACOS COSTA
  192792. DAI, WEI
  192793. GUY, RODNEY KIPLIN
  192794. Angew. Chem. Int. Ed. Engl. 
  192795. A REVIEWM
  192796. 14958N
  192797. 2/28/96
  192798. A CHEMISTRY and BIOLOGY OF TAXOL. 
  192799. 13950
  192800. UNVERZAGT, CARLO
  192801. Angew. Chem. Int. Ed. Engl. C
  192802. A REVIEWM
  192803. 14959N
  192804. 2/28/96
  192805. A0A SUGAR
  192806. BASED DESIGNER DRUG AGAINST INFLUENZA?  
  192807. 1993X
  192808. 1691-3Y
  192809. 13951
  192810. PRAKASH, Om
  192811. SINGH, Shiv P. 
  192812. Aldrichimica ActaC
  192813. A REVIEWM
  192814. 14960N
  192815. 2/28/96
  192816. AjIODOBENZENE DIACETATE and RELATED HYPERVALENT IODINE REAGENTS IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. 
  192817. 1994X
  192818. 1523Y
  192819. 13952
  192820. A4JUARISTI, EUSEBIO
  192821. QUINTANA, DELIA
  192822. ESCALANTE, JAIME. 
  192823. Aldrichimica ActaC
  192824. A REVIEWM
  192825. 14961N
  192826. 2/28/96
  192827. A-ENANTIOSELECTIVE SYNTHESIS OF 
  192828. AMINO ACIDS. 
  192829. 1994X
  192830. 3-11Y
  192831. 13953
  192832. JONES, J. BRYAN
  192833. Aldrichimica ActaC
  192834. A REVIEWM
  192835. 14962N
  192836. 2/28/96
  192837. A9PROBING THE SPECIFICITY OF SYNTHETICALLY USEFUL ENZYMES. 
  192838. 1994X
  192839. 105-112Y
  192840. 13954
  192841. TOMALIA, DONALD A. 
  192842. Aldrichimica ActaC
  192843. A REVIEWM
  192844. 14963N
  192845. 2/28/96
  192846. A_STARBURST
  192847. /CASCADE DENDRIMERS: FUNDAMENTAL BUILDING BLOCKS FOR A NEW NANOSCOPIC CHEMISTRY SET. 
  192848. 1994X
  192849. 91-101Y
  192850. 13955
  192851. A9BORDEN, WESTON THATCHER
  192852. IWAMURA, HIIZU
  192853. BERSON, JEROME A. 
  192854. Acc. Chem. Res.C
  192855. A REVIEWM
  192856. 14964N
  192857. 2/28/96
  192858. AlVIOLATIONS OF HUND'S RULE IN NON
  192859. KEKULE HYDROCARBONS: THEORETICAL PREDICTION and EXPERIMENTAL VERIFICATION. 
  192860. 1994X
  192861. 109-16Y
  192862. 13956
  192863. PARSONS, SIMON
  192864. PASSMORE, JACK
  192865. Acc. Chem. Res.C
  192866. A REVIEWM
  192867. 14965N
  192868. 2/28/96
  192869. A=RINGS, RADICALS, and SYNTHETIC METALS: THE CHEMISTRY OF SNS+ 
  192870. 1994X
  192871. 101-8Y
  192872. 13957
  192873. A6GRIESBECK, AXEL G.
  192874. MAUDER, HARALD
  192875. STADTMUELLER, STEFAN
  192876. Acc. Chem. Res.C
  192877. A REVIEWM
  192878. 14966N
  192879. 2/28/96
  192880. INTERSYSTEM CROSSING IN TRIPLET 1,4
  192881. BIRADICALS: CONFORMATIONAL MEMORY EFFECTS ON THE STEREOSELECTIVITY OF PHOTOCYCLOADDITION REACTIONS. 
  192882. 1994X
  192883. 13958
  192884. GERSON, FABIAN
  192885. Acc. Chem. Res.C
  192886. A REVIEWM
  192887. 14967N
  192888. 2/28/96
  192889. AGAPPLICATIONS OF ENDOR SPECTROSCOPY to RADICAL CATIONS IN EON MATRIXES. 
  192890. 1994X
  192891. 63-9Y
  192892. 13959
  192893. A"ADAM, WALDEMAR
  192894. RICHTER, MARKUS J. 
  192895. Acc. Chem. Res.C
  192896. A REVIEWM
  192897. 14968N
  192898. 2/28/96
  192899. A8METAL
  192900. CATALYZED DIRECT HYDROXY
  192901. EPOXIDATION OF OLEFINS.  
  192902. 1994X
  192903. 57-62Y
  192904. 13960
  192905. AeSESSLER, JONATHAN L.
  192906. HEMMI, GREGORY
  192907. MODY, TARAK D.
  192908. MURAI, TOSHIAKI
  192909. BURRELL, ANTHONY
  192910. YOUNG, STUART W. 
  192911. Acc. Chem. Res.C
  192912. A REVIEWM
  192913. 14969N
  192914. 2/28/96
  192915. A)TEXAPHYRINS: SYNTHESIS and APPLICATIONS. 
  192916. 1994X
  192917. 43-50Y
  192918. 13961
  192919. PADDON
  192920. ROW, MICHAEL N. 
  192921. Acc. Chem. Res.C
  192922. A REVIEWM
  192923. 14970N
  192924. 2/28/96
  192925. INVESTIGATING LONG
  192926. RANGE ELECTRON
  192927. TRANSFER PROCESSES WITH RIGID, COVALENTLY LINKED DONOR
  192928. (NORBORNYLOGOUS BRIDGE)
  192929. ACCEPTOR SYSTEMS. 
  192930. 1994X
  192931. 25. Y
  192932. 13962
  192933. A*POSS, CHRISTOPHER S.
  192934. SCHREIBER, STUART L. 
  192935. Acc. Chem. Res.C
  192936. A REVIEWM
  192937. 14971N
  192938. 2/28/96
  192939. A>TWO
  192940. DIRECTIONAL CHAIN SYNTHESIS and TERMINUS DIFFERENTIATION. 
  192941. 1994X
  192942. 9-17Y
  192943. 13963
  192944. WILLIAMS
  192945. J.C.S. Chem. Commun.CoSILYL SULFONYL PHENYLSULFONYL REDUCTION DIENE DIELS
  192946. ALDER ACETYLENE CYCLOADDITION EQUIVALENT DESILYLSULFONATIONM
  192947. 14972N
  192948. 2/28/96
  192949. BENZENESULFONYL TRIMETHYLSILYL ACETYLENE AS A NEW ACETYLENE EQUIVALENT FOR THE DIELS
  192950. ALDER REACTION
  192951. 1994 X
  192952. 13964
  192953. A    MARTINEZ 
  192954. SynlettC:KETONE ENOL TRIFLATE PALLADIUM COUPLING THIO VINYL SULFIDEM
  192955. 14973N
  192956. 2/28/96
  192957. AdREGIOSELECTIVE SYNTHESIS OF ALKENYL SULFIDES FROM ALKENYL TRIFLATES USING PALLADIUM(0) AS A CATALYST
  192958. 1994 X
  192959. 13965
  192960. TIETZE
  192961. SynlettCiDITHIANE ENANTIOSELECTIVITY DIOL LITHIATE CARBANION EPOXIDE RING OPENING BISALKYLATION TANDEM CROWN ETHERM
  192962. 14974N
  192963. 2/28/96
  192964. AeTANDEM BIS ALKYLATION OF TRIALKYL SILYL
  192965. DITHIANE.  PREPARATION OF 1,5
  192966. DIOLS and DIHYDROXY KETONES
  192967. 1994 X
  192968. 13966
  192969. KATSUKI 
  192970. SynlettCSEPOXIDE EPOXIDATION MANGANESE SALEN ENANTIOSELECTIVITY MECHANISM SELECTIVITY FACIALM
  192971. 14975N
  192972. 2/28/96
  192973. A]HOW DOES CHIRAL OXO(SALEN) MANGANESE V COMPLEX DISCRIMINATE THE ENANTIOFACE OF SIMPLE OLEFINS
  192974. 1994 X
  192975. 13967
  192976. MOODY 
  192977. Tet. Lett.CnDIAZO CARBENOID RHODIUM INSERTION OH SOLVENT DIASTEREOSELECTIVITY ASYMMETRIC ENANTIOSELECTIVITY METALLO CHIRALM
  192978. 14976N
  192979. 2/28/96
  192980. DIASTEREOSELECTIVITY IN THE OH INSERTION REACTIONS OF RHODIUM CARBENOIDS DERIVED FROM PHENYL DIAZO ACETATES OF HOMOCHIRAL ALCOHOLS
  192981. 1994 X
  192982. 13968
  192983. KANEMATSU 
  192984. Tet. Lett.CLFURAN INTRAMOLECULAR DIELS
  192985. ALDER OXABICYCLIC RING OPENING ELIMINATION TARGETM
  192986. 14977N
  192987. 2/28/96
  192988. ARSYNTHETIC STRATEGY FOR THE CONSTRUCTION OF THE FURANOHYDROPHENANTHRENE RING SYSTEM
  192989. 1994 X
  192990. 13969
  192991. DECHOUX 
  192992. Tet. Lett.CyDONOR ACCEPTOR CYCLOPROPANE RING OPENING EPOXIDE ELECTROPHILIC DIACTIVATION INTRODUCTION HOMO MICHAEL ADDITION STEREOCHEMM
  192993. 14978N
  192994. 2/28/96
  192995. ADDIASTEREOSELECTIVE CONTROL IN THE OPENING OF ACTIVATED CYCLOPROPANES
  192996. 1994 X
  192997. 13970
  192998. ZARD 
  192999. Tet. Lett.CEAMIDE LACTAM RADICAL CYCLIZATION HETEROCYCLE METAL TIN INTRAMOLECULARM
  193000. 14979N
  193001. 2/28/96
  193002. APA VERSATILE RADICAL BASED SYNTHESIS OF g-LACTAMS USING NICKEL POWDER ACETIC ACID
  193003. 1994 X
  193004. 13971
  193005. CHAMBERLIN
  193006. Tet. Lett.C6 AZIRIDINYL CARBANION ANION REDUCTION ALKYLATION AMINOM
  193007. 14980N
  193008. 2/28/96
  193009. AMINO AZIRIDINE HYDRAZONES.  HIGHLY DIASTEREOSELECTIVE ALKYLATION WITHOUT CHELATION and A SYN DIRECTING EFFECT
  193010. 1994 X
  193011. 13972
  193012. WULFF
  193013. JACSC
  193014. BENZANNULATION VINYLKETENE QUINONE CARBENOID INSERTION CARBON MONOXIDE CYCLOPROPENE WRITING INTRODUCTION MOLYBDENUM AROMATIC PHENOLM
  193015. 14981N
  193016. 2/28/96
  193017. AuMETAL CATALYZED CYCLOPROPENE REARRANGEMENTS FOR BENZANNULATION.  ANTHRAQUINONE SYNTHESIS VIA CARBENE
  193018. CHROMIUM COMPLEX
  193019. 1994X
  193020. 7108Y
  193021. 13973
  193022. MOORE 
  193023. Tet. Lett.C=TRIAZENE DIAZONIUM ION IODIDE ARYL PHENYL MASK THERMAL METHODM
  193024. 14983N
  193025. 2/28/96
  193026. AdIODINE PROMOTED DECOMPOSITION OF DIALKYL TRIAZENES.  A MILD METHOD FOR THE SYNTHESIS OF ARYL IODIDES
  193027. 1994 X
  193028. 13975
  193029. A    KULKARNI 
  193030. Tet. Lett.CfNITRILE OXIDES PREPARATION NITRO ALKENE REDUCTION CHLORO TITANIUM TETRACHLORIDE ISOXAZOLINES MUKAIYAMAM
  193031. 14984N
  193032. 2/28/96
  193033. AhA FACILE CONVERSION OF NITRO OLEFINS to FUNCTIONALIZED HYDROXIMOYL CHLORIDES AS NITRILE OXIDE PRECURSORS
  193034. 1994 X
  193035. 13976
  193036. WIGHTMANN 
  193037. Tet. Lett.CrNITRONE SUGAR RIBASE SHIKIMIC BIOSYNTHETIC TARGET HYDROGENATION PERLMAN CATALYST CLEAVAGE  ISOXAZOLIDINE REDUCTIONM
  193038. 14985N
  193039. 2/28/96
  193040. AUUSE OF AN INTRAMOLECULAR DIPOLAR NITRONE CYCLOADDITION FOR SYNTHESIS OF SHIKIMIC ACID
  193041. 1994 X
  193042. 13977
  193043. RAVINDRANATHAN 
  193044. Tet. Lett.CFOXIME CONVERSION HYDROLYSIS REAGENT CLEAVAGE CATALYTIC CARBONYL KETONEM
  193045. 14986N
  193046. 2/28/96
  193047. AFSELECTIVE CATALYTIC OXIDATIVE CLEAVAGE OF OXIMES to CARBONYL COMPOUNDS
  193048. 1994 X
  193049. 13978
  193050. BADONE 
  193051. Tet. Lett.C8TIN ALLENE COUPLING TRIFLATE PALLADIUM ARYL CROSS STILLEM
  193052. 14987N
  193053. 2/28/96
  193054. AdTHE STILLE COUPLING REACTION OF ARYL TRIFLATES WITH ALLENE STANNANE.  A GENERAL ROUTE to ARYLALLENES
  193055. 1994 X
  193056. 13979
  193057. FALCK 
  193058. Tet. Lett.CXSULFONIUM YLIDE DISPLACEMENT HALIDE ALKENE ELIMINATION VINYL GROUP SYNTHESIS PREPARATIONM
  193059. 14988N
  193060. 2/28/96
  193061. A1SULFUR YLIDE VINYLATION OF HALIDES and MESYLATION
  193062. 1994 X
  193063. 13980
  193064. FALCK 
  193065. Tet. Lett.C@EPOXIDE RING OPENING SULFONIUM YLIDE ALLYLIC ALCOHOL ELIMINATIONM
  193066. 14989
  193067. 2/28/96
  193068. AgNOVEL CONVERSION OF EPOXIDES to ONE CARBON HOMOLOGATED ALLYLIC ALCOHOLS BY DIMETHYL SULFONIUM METHYLIDE
  193069. 1994 X
  193070. 13981
  193071. FALCK 
  193072. Tet. Lett.CGDESULFONYLATION BIS SULFONE SULFONYL CARBANION ADDITION CARBONYL KETONEM
  193073. 14990N
  193074. 2/28/96
  193075. ACSAMARIUM IODIDE REDUCTIVE ADDITION OF BIS
  193076. PHENYLSULFONES to KETONES
  193077. 1994 X
  193078. 13982
  193079. SESTANJ 
  193080. Tet. Lett.CTOPIOD BANKS FROG ANALGESIC AZABICYCLIC CUPRATE ADDITION OXIME REDUCTION DETOSYLATIONM
  193081. 14991N
  193082. 2/28/96
  193083. ALSYNTHESIS OF RACEMIC EPIBATIDINE 
  193084.  A NATURAL PRODUCT WITH ANALGESIC ACTIVITY
  193085. 1994 X
  193086. 13983
  193087. A    SINGARAM 
  193088. Tet. Lett.CfHYDRIDE REAGENT REDUCTION IMINE CHIRAL ASYMMETRIC DIASTEREOSELECTIVITY ENANTIOSELECTIVE ALKALOID AMINEM
  193089. 14992N
  193090. 2/28/96
  193091. A`DIASTEREOSELECTIVE REDUCTION OF THE CARBON
  193092. NITROGEN DOUBLE BOND OF IMINES USING HYDRIDE REAGENTS
  193093. 1994X
  193094. 13984
  193095. GRIMM 
  193096. Tet. Lett.
  193097. SULFONE CARBANION ESTER ADDITION CYCLIZATION TARGET NICKEL REPLACEMENT WRITING VINYL NOVEL TRANSITION METAL METHYL DISPLACEMENT GRIGNARDM
  193098. 14993N
  193099. 2/28/96
  193100. AaBICYCLIC SESQUITERPENE SYNTHESIS VIA INTRAMOLECULAR CYCLIZATION OF A SULFONE STABILIZED CARBANION
  193101. 1994 X
  193102. 13985
  193103. JOCC>PROPARGYL HALIDE ELIMINATION VINYLIDENE CARBENE ALLENE ALCOHOLM
  193104. 14994N
  193105. 2/28/96
  193106. NEW METHOD FOR GENERATION OF ALKYLIDENECARBENES FROM  PROPARGYLIC METHANESULFONATES and ITS USE IN REGIOSELECTIVE C
  193107. H INSERTION REACTIONS
  193108. 1994X
  193109. 4010Y
  193110. 13986
  193111. STERNER 
  193112. JOCCE1,4
  193113. DIALDEHYDE DIELS
  193114. ALDER FURAN OXABICYCLIC RING OPENING CYCLOHEXENEM
  193115. 14995N
  193116. 2/28/96
  193117. AQSYNTHESIS OF CYCLOHEXENE
  193118. DICARBALDEHYDES VIA DIELS ALDER REACTIONS WITH FURAN
  193119. 1994X
  193120. 3994Y
  193121. 13987
  193122. PARKER 
  193123. MORPHINE TARGET CONVERGENT RADICAL AROMATIC CYCLIZATION THIOPHENYL ADDITION ELIMINATION INTRAMOLECULAR TANDEM STEREOCHEM ANALYSISK
  193124. SEE FOLLOWING ARTICLE.M
  193125. 14996N
  193126. 2/28/96
  193127. A_STEREOCHEMISTRY OF RADICAL CYCLIZATIONS to SIDE CHAIN OLEFINIC BONDS AS AN APPROACH to MORPHINE
  193128. 1994X
  193129. 3927Y
  193130. 13988
  193131. OGAWA
  193132. JOCCzALKYNE, DIPHENYLDITELLURIDE, 1,2
  193133. BISTELLUROALKENE, CUPRATE SUBSTITUTION, TELLURIUM
  193134. LITHIUM EXCHANGE, VINYLIC ORGANOLITHIUMM
  193135. 14997N
  193136. 2/28/96
  193137. A6VINYLIC SUBSTITUTION OF VINYL TELLURIDES WITH CUPRATES
  193138. 1994  X    1600
  193139. 1601Y
  193140. 13989
  193141. 14998N
  193142. 2/28/96
  193143. A9COMPUTER ASSISTED EVALUATION OF CARBENE CHEMISTRY 
  193144.  CAMEO
  193145. 1994X
  193146. 3841Y
  193147. 13990
  193148. DITTMER 
  193149. JOCCHEPOXIDE ASYMMETRIC SYNTHESIS TELLURIUM EPOXIDATION SUGAR ALLYLIC ALCOHOLM
  193150. 15000N
  193151. 2/28/96
  193152. AvAPPLICATION OF TELLURIUM CHEMISTRY and SHARPLESS ASYMMETRIC EPOXIDATION to THE SYNTHESIS OF OPTICALLY ACTIVE BOIVINASE
  193153. 1994X
  193154. 4311Y
  193155. 13992
  193156. LABADIE
  193157. JOCC4 INDOLE TIN COUPLING PALLADIUM INTRODUCTION STANNANEM
  193158. 15001N
  193159. 2/28/96
  193160. AKINDOL
  193161. YL TRIBUTYLSTANNANE.  A VERSATILE REAGENT FOR 2
  193162. SUBSTITUTED INDOLES
  193163. 1994X
  193164. 4250Y
  193165. 13993
  193166. LAROCK
  193167. JOCCJ INTRODUCTION WEINREB PALLADIUM CASCADE TANDEM VINYL HECK TOSYL SEQUENTIALM
  193168. 15002N
  193169. 2/28/96
  193170. AuSYNTHESIS OF PYRROLIDINE and PIPERIDINE VIA PALLADIUM CATALYZED COUPLING OF VINYLIC HALIDES and OLEFINIC SULFONAMIDES
  193171. 1994X
  193172. 4172Y
  193173. 13994
  193174. VEDEJS
  193175. JOCCWSAMARIUM IODIDE IN THF / DMPU, SULFONAMIDE DEPROTECTION TO AMINE, AZIRIDINE, AMINO ACIDM
  193176. 15003N
  193177. 2/28/96
  193178. A6DEPROTECTION OF ARENESULFONAMIDES WITH SAMARIUM IODIDE
  193179. 1994  X    1602
  193180. 1603Y
  193181. 13995
  193182. A    JACOBSEN 
  193183. JOCC$MANGANESE SALEN COMPLEX, EPOXIDATIONM
  193184. 15004N
  193185. 2/28/96
  193186. AILARGE
  193187. SCALE PREPARATION OF JACOBSEN'S CATALYST FOR ASYMMETRIC EPOXIDATION
  193188. 1994  X    1939
  193189. 1942Y
  193190. 13996
  193191. A    FLETCHER 
  193192. JOCCG7
  193193. AZABICYCLO[2.2.1]HEPTANE, EPOXIDE OPENING INTRAMOLECULAR, SYN OPENINGM
  193194. 15005N
  193195. 2/28/96
  193196. ANTOTAL SYNTHESIS and DETERMINATION OF THE ABSOLUTE CONFIGURATION OF EPIBATIDINE
  193197. 1994  X    1771
  193198. 1778Y
  193199. 13997
  193200. OLAFSON 
  193201. ANTHRACENE ISOCOUMARIN ORTHO ALDEHYDE CARBANION ADDITION TANDEM BENZOCYCLOBUTENOL RING OPENING TARGET BIMOLECULAR AROMATIC WRITINGM
  193202. 15006N
  193203. 2/28/96
  193204. ATREACTION OF BENZOCYCLOBUTENOXIDES WITH ALDEHYDES.  SYNTHESIS OF DIHYDRO ISOCOUMARINS
  193205. 1994X
  193206. 4117Y
  193207. 13998
  193208. HOYE 
  193209. #CVNMR SPECTROSCOPY MULTIPLET FIRST ORDER COUPLING CONSTANT 2D MULTISPIN COMPLEX SPECTRUMM
  193210. 15007N
  193211. 2/28/96
  193212. AGA PRACTICAL GUIDE to FIRST ORDER MULTIPLET ANALYSIS IN NMR SPECTROSCOPY
  193213. 1994X
  193214. 4096Y
  193215. 13999
  193216. WARKENTIN 
  193217. JOCC\CARBENE LACTAM CYCLOBUTANE CYCLOPROPANATION EXTRUSION NITROGEN DIRADICAL AMIDE STABILIZATIONM
  193218. 15008N
  193219. 2/28/96
  193220. AbBIMOLECULAR REACTIONS OF CARBENES IN FOUR MEMBERED RINGS.  SYNTHESIS OF SPIRO LACTAM CYCLOPROPANES
  193221. 1994X
  193222. 4090Y
  193223. 14000
  193224. MORTIER 
  193225. %CRCARBOXYLIC ACID LITHIATE ORTHO LITHIATION DIRECTOR AROMATIC CARBANION ELECTROPHILEM
  193226. 15009N
  193227. 2/28/96
  193228. AFTHE CARBOXYLIC ACID GROUP AS AN EFFECTIVE DIRECTOR OF ORTHO LITHIATION
  193229. 1994X
  193230. 4042Y
  193231. 14001
  193232. A    JACOBSEN 
  193233. JACSC\EPOXIDATION EPOXIDE CATALYST SALEN MN MANGANESE ENANTIOSELECTIVE CHIRAL INDUCTION ASYMMETRICM
  193234. 15010N
  193235. 2/28/96
  193236. EFFECT OF CHIRAL QUATERNARY AMMONIUM SALTS ON SALEN MANGANESE CATALYZED EPOXIDATION OF CIS
  193237. OLEFINS.  A HIGHLY ENANTIOSELECTIVE, CATALYTIC ROUTE to TRANS EPOXIDES
  193238. 1994 X
  193239. 6937Y
  193240. 14002
  193241. DAVIES
  193242. Tet. Lett.CyDIAZO PYRROLE INTRAMOLECULAR RHODIUM STEPWISE RING OPENING NOVEL ELECTROCYCLIZATION CYCLOBUTENE MECHANISM CARBENOID VINYLM
  193243. 15011N
  193244. 2/28/96
  193245. RHODIUM(II) CATALYZED INTRAMOLECULAR REACTIONS BETWEEN VINYLDIAZOMETHANES and PYRROLES NOVEL SYNTHESIS OF FUSED AZABICYCLOOCTADIENES
  193246. 1994 X
  193247. 14003
  193248. Tet. Lett.M
  193249. 15012N
  193250. 2/28/96
  193251. ASENANTIOSELECTIVE 2,3
  193252. WITTIG REARRANGEMENT INVOLVING A CHIRAL BORON ENOLATE TERMINUS
  193253. 1994 X
  193254. 14004
  193255. Tet. Lett.
  193256. )CU INTRAMOLECULAR PYRIDAZINE DIELS
  193257. ALDER EXTRUSION NITROGEN ALKYNE TARGET SESQUITERPENEM
  193258. 15013N
  193259. 2/28/96
  193260. SYNTHETIC APPROACH to CUPARANE and HERBERTANE SESQUITERPENOIDS BY AN INTRAMOLECULAR DIELS
  193261. ALDER REACTION OF A DIAZADIENE HETEROCYCLE
  193262. 1994 X
  193263. 14005
  193264. RATAVELOMANANA 
  193265. Tet. Lett.CBBROMO ALKYNE BASE DEHYDROBROMINATION EXPERIMENTAL METHOD ACETYLENEM
  193266. 15014N
  193267. 2/28/96
  193268. AoDEHYDROBROMINATION OF 1,1
  193269. DIBROMOOLEFINS AS A GENERAL SYNTHESIS OF BROMO AROMATIC ALKYNES UNDER MILD CONDITIONS
  193270. 1994 X
  193271. 14006
  193272. JEFFORD
  193273. Tet. Lett.CD INDOLIZIDINE ALKALOID PYRROLE REDUCTION TIN REDUCTION FRIEDEL CRAFTM
  193274. 15015N
  193275. 2/28/96
  193276. AiENANTIOSELECTIVE SYNTHESIS OF INDOLIZIDINE ALKALOIDS BY BORON TRIBROMIDE INDUCED CYCLIZATION OF A PYRROLE
  193277. 1994 X
  193278. 14007
  193279. ATTARDO
  193280. Tet. Lett.CM SO2 SULFUR DIOXIDE EXTRUSION ADDITION O
  193281. QUINODIMETHANE REARRANGEMENT SULTINEM
  193282. 15016N
  193283. 2/28/96
  193284. A_EFFICIENT SYNTHESIS OF O
  193285. QUINODIMETHANES and SO2 to PREPARE DIHYDROBENZOTHIOPHENES 2,2
  193286. DIOXIDES
  193287. 1994 X
  193288. 14008
  193289. SHIORI 
  193290. SynlettCGCARBENE VINYL DIAZO ACETYLENE REARRANGEMENT TRIMETHYLSILYL DIHYDROFURANM
  193291. 15017N
  193292. 2/28/96
  193293. AqA NEW SYNTHESIS OF TRIMETHYLSILYL DIHYDROFURANS FROM TRIMETHYLSILOXYKETONES UTILIZING TRIMETHYLSILYL DIAZOMETHANE
  193294. 1994 X
  193295. 14009
  193296. DavisB
  193297. J. Org. ChemCo Aziridine, Hydroxy amino acid, diastereomer, darzens, chiral, asymmetric, sulfinimide, ring opening, synthesisM
  193298. 15018N
  193299. 2/28/96
  193300. ATAsymmetric Synthesis and Reactions OF p-Toluenesulfinyl Aziridine 2-Carboxylic Acids
  193301. 1994X
  193302. 3243 Y
  193303. 14010
  193304. TANNER
  193305. Tet. Lett.CQ AZIRIDINE CHIRAL LIGAND TRANSITION METAL LACTAM CUPRATE TOSYL ENANTIOSELECTIVITYM
  193306. 15019N
  193307. 2/28/96
  193308. SYMMETRIC BIS AZIRIDINES 
  193309.  A NEW CLASS OF CHIRAL LIGANDS FOR TRANSITION METAL MEDIATED ASYMMETRIC SYNTHESIS
  193310. 1994 X
  193311. 14011
  193312. J.C.S. Chem. Commun.Cf CYCLOPROPENE RING OPENING VINYL CARBENE NOVEL INSERTION MECHANISM ALKYLIDENE VINYLIDENE REARRANGEMENTM
  193313. 15020N
  193314. 2/28/96
  193315. AeNEW EVIDENCE FOR THE INVOLVEMENT OF ALKYLIDENE CARBENES IN THE THERMAL ISOMERIZATION OF CYCLOPROPENES
  193316. 1994 X
  193317. 14012
  193318. SHIBUYA 
  193319. J.C.S. Chem. Commun.CYRADICAL CYCLIZATION TIN INTRAMOLECULAR TARGET KETYL HETEROCYCLIC CHIRAL ASYMMETRIC LACTAMM
  193320. 15021N
  193321. 2/28/96
  193322. AdA NEW ROUTE to CHIRAL PYRROLIDINES VIA RADICAL CYCLIZATION.  ENANTIOSELECTIVITY USING OXAZOLIDINONES
  193323. 1994 X
  193324. 14013
  193325. BALASUBRAMANIAN
  193326. J.C.S. Chem. Commun.CSALLENE AMINO AMINE OXIDE 2,3
  193327. SIGMATROPIC 3,3 COPE INDOLE REARRANGEMENT VINYL COURSEM
  193328. 15022N
  193329. 2/28/96
  193330. A3TANDEM TRANSFORMATIONS OF ALLENYL AMINES to INDOLES
  193331. 1994 X
  193332. 14014
  193333. DEKIMPE
  193334. J.C.S. Chem. Commun.CI AZIRIDINE RADICAL RING OPENING SONOCHEMISTRY CLEAVAGE ZINC REARRANGEMENTM
  193335. 15023N
  193336. 2/28/96
  193337. AFSONOCHEMICAL CLEAVAGE OF BROMOMETHYL AZIRIDINE BY A ZINC COPPER COUPLE
  193338. 1994 X
  193339. 14015
  193340. KATRITZKY, A. R.
  193341. B    SynthesisCcN
  193342. SUBSTITUTED BENZOTRIAZOLES REGIOSELECTIVE SUBSTITUTION HYDROLYSIS DECARBOXYLATION N
  193343. ALKYLATION M
  193344. 15024N
  193345. 2/28/96
  193346. A SIMPLE, VERSATILE SYNTHETIC ROUTE to N
  193347. HETEROARYL
  193348. ACYLMETHYL
  193349. CARBOXYMETHYL
  193350.  and 
  193351. ALKYL
  193352. BENZOTRIAZOLES VIA REGIOSPECIFIC OR HIGHLY REGIOSELECTIVE SUBSTITUTIONS OF TRIAZOLE
  193353. 1994 X
  193354. 14016
  193355. MCGAFFIN, G.
  193356. B    SynthesisC
  193357. PALLADIUM
  193358. CATALYZED VINYLATION ACETYLENE DERIVATIVES ORGANIC HALIDES CHIRAL LIGANDS ALKYNES OLEFINS COMPLEXES REAGENTS NICKEL ENYNES M
  193359. 15025N
  193360. 2/28/96
  193361. PALLADIUM(0)
  193362. CATALYZED COUPLING REACTIONS OF 2
  193363. ALKOXY
  193364. ETHYNYLCYCLOPROPANES, WITH ARYL and ETHENYL HALIDES:  PREPARATION OF CYCLOPROPYL SUBSTITUTED ETHYNYLARENES, ENEYNES and ENEDIYNES
  193365. 1994 X
  193366. 14017
  193367. VIJN, R. J.
  193368. B    SynthesisC^DIELS
  193369. ALDER REACTIONS DERIVATIVES HYDRAZONES PYRIDINE
  193370. DICARBOXIMIDES 1
  193371. BUTADIENES M
  193372. 15026N
  193373. 2/28/96
  193374. AqSYNTHESIS OF ALKYL
  193375.  and ARYL
  193376. SUBSTITUTED PYRIDINES FROM (A,b
  193377. UNSATURATED) IMINES OR OXIMES and CARBONYL COMPOUNDS
  193378. 1994 X
  193379. 14018
  193380. ADAM, W.
  193381. B    Synthesis
  193382. GAMMA
  193383. HYDROXY VINYLSTANNANES PHOTOOXYGENATION SINGLET OXYGEN ENE REACTION (SCHENCK REACTION) CARBONYLATION ALPHA
  193384. ALKYLIDENE
  193385. HYDROXY
  193386. GAMMA
  193387. BUTYROLACTONES PALLADIUM
  193388. CATALYZED CARBONYLATION 1,2
  193389. TRANSPOSED ALLYLIC ALCOHOLS ASYMMETRIC REDUCTION ORGANIC
  193390. SYNTHESIS KETONES 
  193391. 15027N
  193392. 2/28/96
  193393. ALKYLIDENE
  193394. DIHYDRO
  193395. HYDROXY
  193396. METHYL
  193397. FURANONES BY REGIO
  193398.  and DIASTEREOSELECTIVE ENE REACTION OF SINGLET OXYGEN (SCHENK REACTION) WITH g
  193399. HYDROXY VINYLSTANNANES:  AN ENANTIOSELECTIVE SYNTHESIS OF DIHYDROMAHUBANOLIDE B
  193400. 1994 
  193401. 14019
  193402. ADAM, W.
  193403. B    SynthesisChVINYLSTANNANES ALPHA
  193404. STANNYL ENONES PHOTOOXYGENATION ALLYLIC HYDROPEROXIDES DEHYDRATION HYDROSTANNATION M
  193405. 15028N
  193406. 2/28/96
  193407. A CONVENIENT STEREOSELECTIVE SYNTHESIS OF A
  193408. TRIBUTYLSTANNYL ENONES BY PHOTOOXYGENATION OF VINYLSTANNANES and DEHYDRATION OF THE RESULTING HYDROPEROXIDES
  193409. 1994X
  193410. 14020
  193411. WALDMANN, H.
  193412. B    Synthesis
  193413. NITROSO
  193414. COMPOUNDS ALPHA
  193415. CHLORONITROSO COMPOUNDS NATURAL PRODUCT SYNTHESIS CYCLO
  193416. ADDITION REACTIONS ORGANO
  193417. ALUMINUM REAGENT AMINO
  193418. ACID DERIVATIVES CHIRAL LEWIS ACID ACYLNITROSO DIENOPHILES ENANTIOSELECTIVE SYNTHESIS AQUEOUS
  193419. SOLUTION M
  193420. 15029N
  193421. 2/28/96
  193422. A'ASYMMETRIC HETERO DIELS
  193423. ALDER REACTIONS
  193424. 1994 X
  193425. 14021
  193426. SILVEIRA, C. C.
  193427. Syn. Commun.C
  193428. CYCLOPROPANES M
  193429. 15030N
  193430. 2/28/96
  193431. AUARYLSELENO and 1
  193432. CHLORO
  193433. ARYLSELENO CYCLOPROPANES FROM PTC and ULTRASOUND CONDITIONS
  193434. 1994X    2075
  193435. 2080Y
  193436. 14022
  193437. THANGARAJ, K.
  193438. Syn. Commun.M
  193439. 15031N
  193440. 2/28/96
  193441. ALKYLATION OF AROMATIC and HETEROAROMATIC
  193442. DINITROPHENYLHYDRAZONES WITH POTASSIUM FLUORIDE ON ALUMINA
  193443. 1994X    2063
  193444. 2067Y
  193445. 14023
  193446. A    CAINE, D.
  193447. Syn. Commun.M
  193448. 15032N
  193449. 2/28/96
  193450. AQINTRODUCTION OF AN ISOPROPYL GROUP AT THE g POSITION OF A HYDRINDENONE DERIVATIVE
  193451. 1994X    2039
  193452. 2048Y
  193453. 14024
  193454. TARASOVA, O. A.
  193455. Syn. Commun.M
  193456. 15033N
  193457. 2/28/96
  193458. A6AN EFFICIENT PROCEDURE FOR THE N
  193459. VINYLATION OF PYRROLE
  193460. 1994X    2035
  193461. 2037Y
  193462. 14025
  193463. DAMOUR, D.
  193464. Syn. Commun.M
  193465. 15034N
  193466. 2/28/96
  193467. ARA NOVEL and EFFICIENT APPROACH to THE SYNTHESIS OF 4
  193468. AMINO
  193469. CYCLOPENT
  193470. 1994X    2017
  193471. 2027Y
  193472. 14026
  193473. BELTAIEF, I.
  193474. Syn. Commun.C]ETHYL ALPHA
  193475. (HYDROXYMETHYL)ACRYLATE RAPID SYNTHESIS ESTERS COPPER(I) ALDEHYDES LITHIUM SALTS M
  193476. 15035N
  193477. 2/28/96
  193478. AfSUBSTITUTION OF ALLYLIC FUNCTIONAL ACETATES 
  193479.  STEREOSELECTIVE SYNTHESIS OF 2
  193480. ALKYLIDENE
  193481. KETOESTERS
  193482. 1994X    2003
  193483. 2010Y
  193484. 14027
  193485. KAYE, P. T.
  193486. Syn. Commun.CRFRAGMENTATION PATTERNS MASS
  193487. SPECTRA 3,4
  193488. DIHYDRO
  193489. PHENYL
  193490. BENZODIOXEPIN
  193491. ONES M
  193492. 15036N
  193493. 2/28/96
  193494. A\REGIOSELECTIVE A
  193495. RING CHLORINATION OF BENZODIAZEPINE ANALOGUES USING TERT
  193496. BUTYL HYPOCHLORITE
  193497. 1994X    1971
  193498. 1978Y
  193499. 14028
  193500. IRANPOOR, N.
  193501. Syn. Commun.C!AMMONIUM
  193502. NITRATE MILD CONVERSION M
  193503. 15037N
  193504. 2/28/96
  193505. TRIS[TRINITRATO CE(IV)]PARAPERIODATE, AN EFFICIENT HETEROGENEOUS CATALYST FOR ALCOHOLYSIS, ACETOLYSIS and HYDROLYSIS OF EPOXIDES
  193506. 1994X    1959
  193507. 1969Y
  193508. 14029
  193509. GADAGINAMATH, G. S.
  193510. Ind. J. Chem. Sect. BM
  193511. 15038N
  193512. 2/28/96
  193513. AxSTUDIES ON CLAISEN REARRANGEMENT OF SUBSTITUTED 5
  193514. ALLYLOXYINDOLES, FUROINDOLE SYNTHESIS and THEIR ANTIMICROBIAL ACTIVITY
  193515. 1994 X
  193516. 14030
  193517. KUMARI, A. S.
  193518. Ind. J. Chem. Sect. BM
  193519. 15039N
  193520. 2/28/96
  193521. ANREACTIONS OF N
  193522. PYRROLIDINOCYCLOALKENES WITH 2
  193523. PHENYL
  193524. BENZYLIDENE
  193525. OXAZOLONE
  193526. 1994X
  193527. 14031
  193528. DHILLON, R. S.
  193529. Ind. J. Chem. Sect. BCNFIR TUSSOCK MOTH SEX
  193530. PHEROMONE STEREOSPECIFIC SYNTHESIS HYDROBORATION REAGENT M
  193531. 15040N
  193532. 2/28/96
  193533. A\PHEROMONES VIA ORGANOBORANES .3. A SHORT and CONVENIENT SYNTHESIS OF (Z)
  193534. HENEICOSEN
  193535. 1994 X
  193536. 14032
  193537. IKRAMUDDEEN, T. M.
  193538. Ind. J. Chem. Sect. BM
  193539. 15041N
  193540. 2/28/96
  193541. A0A NOVEL SYNTHESIS OF 2 N
  193542. SUBSTITUTED PIPERIDONES
  193543. 1994 X
  193544. 14033
  193545. SRIVASTAVA, V.
  193546. Ind. J. Chem. Sect. BM
  193547. 15042N
  193548. 2/28/96
  193549. ALNEW BRIDGEHEAD NITROGEN HETEROCYCLES OF FURAN AS POTENT ANTIMICROBIAL AGENTS
  193550. 1994 X
  193551. 14034
  193552. BUBNOV, Y. N.
  193553. Pure Appl. Chem.M
  193554. 15043N
  193555. 2/28/96
  193556. A^REDUCTIVE MONO
  193557. A and TRANS
  193558. DIALLYLATION OF AROMATIC NITROGEN HETEROCYCLES BY ALLYLBORANES
  193559. 1994 X
  193560. 14035
  193561. SUZUKI, A.
  193562. Pure Appl. Chem.C
  193563. CROSS
  193564. COUPLING REACTION ALKYL GRIGNARD
  193565. REAGENTS 9
  193566. ALKYL
  193567. BBN DERIVATIVES (DIALKOXYBORYL)METHYLZINC REAGENTS STEREOSELECTIVE SYNTHESIS HALOARENES KETONES IODIDES ARYL HALIDES M
  193568. 15044N
  193569. 2/28/96
  193570. A7NEW SYNTHETIC TRANSFORMATIONS VIA ORGANOBORON COMPOUNDS
  193571. 1994X
  193572. 14036
  193573. BROWN, H. C.
  193574. Pure Appl. Chem.C
  193575. HIGH OPTICAL PURITY HIGH ENANTIOMERIC PURITIES CHIRAL REDUCING AGENT SELECTIVE REDUCTIONS ALPHA,BETA
  193576. ACETYLENIC KETONES PROCHIRAL KETONES STERIC REQUIREMENTS HOMOALLYL ALCOHOLS ORGANOBORANES ESTERS M
  193577. 15045N
  193578. 2/28/96
  193579. A:RECENT ADVANCES IN THE BORON ROUTE to ASYMMETRIC SYNTHESIS
  193580. 1994 X
  193581. 14037
  193582. MULLER, P.
  193583. Pure Appl. Chem.M
  193584. 15046N
  193585. 2/28/96
  193586. A4GLOSSARY OF TERMS USED IN PHYSICAL ORGANIC CHEMISTRY
  193587. JX    1077
  193588. 1184Y
  193589. 14038
  193590. Ito, M.B
  193591. Pure Appl. Chem.C
  193592. PERIDININ CHROMOPHOREM
  193593. 15047N
  193594. 2/28/96
  193595. A4RECENT PROGRESS IN CAROTENOID and RETINOID SYNTHESIS
  193596. 1994 X
  193597. 14039
  193598. A    MAYER, H.
  193599. Pure Appl. Chem.C
  193600. STRUCTURALLY RELATED
  193601. COMPOUNDS ACTIVE NATURAL CAROTENOIDS TECHNICAL PROCEDURES BETA
  193602. CAROTENE (3R,3'R)
  193603. ZEAXANTHIN 6
  193604. ISOPHORONE SALMON M
  193605. 15048N
  193606. 2/28/96
  193607. A#REFLECTIONS ON CAROTENOID SYNTHESIS
  193608. 1994 X
  193609. 14040
  193610. MA    Ge, C. S.B
  193611. J.C.S. Chem. Commun.C
  193612. LASER FLASH
  193613. PHOTOLYSIS 1,2
  193614. HYDROGEN MIGRATION ABSOLUTE RATE HYDROGEN MIGRATION STATES PHENYLCHLOROCARBENE AMBIPHILICITY REARRANGEMENT SPECTROSCOPY CONSTANT M
  193615. 15049N
  193616. 2/28/96
  193617. A=THE KINETIC RANGE OF CARBENE
  193618. PYRIDINE YLIDE FORMING REACTIONS
  193619. 1994 X    1479
  193620. 1480Z
  193621. 14041
  193622. GREEVES, N.
  193623. J.C.S. Chem. Commun.C)ASYMMETRIC TRANSMISSION DIASTEREOCONTROL M
  193624. 15050N
  193625. 2/28/96
  193626. STEREOCONVERGENT 'ONE POT' TANDEM [2,3]
  193627. WITTIG
  193628. ANIONIC OXY
  193629. COPE REARRANGEMENT OF ACYCLIC BIS
  193630. ALLYLIC ETHERS IN THE DIASTEREOSELECTIVE SYNTHESIS OF SUBSTITUTED TETRAHYDROPYRANS
  193631. 1994 X    1469
  193632. 1470Z
  193633. 14042
  193634. HOPF, H.
  193635. J.C.S. Chem. Commun.CWVINYLIDENE REARRANGEMENTS ISOMERIZATION INTERMEDIACY ACETYLENE PYROLYSIS KINETICS HEAT M
  193636. 15051N
  193637. 2/28/96
  193638. AeNEW EVIDENCE FOR THE INVOLVEMENT OF ALKYLIDENE CARBENES IN THE THERMAL ISOMERISATION OF CYCLOPROPENES
  193639. 1994 X    1467
  193640. 1468Z
  193641. 14043
  193642. TANAKA, H.
  193643. J.C.S. Chem. Commun.CEZINC POWDER ARYL CYCLIZATION PALLADIUM CEPHEMS ALKENYL INSITU NICKEL M
  193644. 15052N
  193645. 2/28/96
  193646. A FACILE ACCESS to 3
  193647. ALLYL
  193648.  AND 3
  193649. BENZYL
  193650. CEPHEMS VIA REDUCTIVE ADDITION/CYCLIZATION OF ALLENECARBOXYLATE WITH ALLYL and BENZYL HALIDES IN AN AL/PB/NI REDOX SYSTEM
  193651. 1994 X    1461
  193652. 1462Z
  193653. 14044
  193654. MASUYAMA, Y.
  193655. J.C.S. Chem. Commun.C
  193656. ALLYLIC SULFONES M
  193657. 15053N
  193658. 2/28/96
  193659. AqPALLADIUM
  193660. CATALYSED CARBONYL ALLYLATION BY ISOPRENE VIA REGIOSELECTIVE 1,4
  193661. ADDITION OF TIN HYDRIDE FORMED IN SITU
  193662. 1994 X    1451
  193663. 1452Z
  193664. 14045
  193665. A    ROLFS, A.
  193666. J.C.S. Chem. Commun.M
  193667. 15054N
  193668. 2/28/96
  193669. CONDENSATION OF ARYLTHIOACETAMIDES:  NOVEL SYNTHESES OF 3
  193670. AMINOTHIOACRYLAMIDES, 2,4
  193671. DIAMINOTHIOPHENES and FOUR
  193672. MEMBERED
  193673. RING VINAMIDINIUM SALTS
  193674. 1994 X    1437
  193675. 1438Z
  193676. 14046
  193677. GABRIELE, B.
  193678. J.C.S. Chem. Commun.M
  193679. 15055N
  193680. 2/28/96
  193681. STEREOSELECTIVE SYNTHESIS OF b
  193682. LACTONES CONTAINING A
  193683. ALKOXYCARBONYLMETHYLENE CHAINS BY PALLADIUM
  193684. CATALYSED OXIDATIVE CARBONYLATION OF TERTIARY A
  193685. HYDROXYALKYNES
  193686. 1994 JUN 21; (12): 1429
  193687. 1430X    1429
  193688. 1430Z
  193689. 14047
  193690. CHATANI, N.
  193691. JACSM
  193692. 15056
  193693. 2/28/96
  193694. AqHIGHLY SELECTIVE SKELETAL REORGANIZATION OF 1,6
  193695.  and 1,7
  193696. ENYNES to 1
  193697. VINYLCYCLOALKENES CATALYZED BY [RUCL2(CO)3]2
  193698. 1994X    6049
  193699. 6050Y
  193700. 14048
  193701. NAIR, H. K.
  193702. JACSM
  193703. 15057N
  193704. 2/28/96
  193705. NOVEL DIALKYL (b
  193706. HALOTETRAFLUOROETHYL)PHOSPHONATES:  FACILE SYNTHESIS VIA THERMALLY and PHOTOCHEMICALLY INDUCED RADICAL REACTIONS. A UNIQUE PHOTOCHEMICAL TRANSFORMATION OF BRCF2CF2I
  193707. 1994 X    6041
  193708. 6042Y
  193709. 14049
  193710. YAMAMOTO, Y.
  193711. JACSM
  193712. 15058N
  193713. 2/28/96
  193714. ATPALLADIUM
  193715. CATALYZED ADDITION OF ACTIVATED METHYLENE and METHYNE COMPOUNDS to ALLENES
  193716. 1994 X    6019
  193717. 6020Y
  193718. 14050
  193719. Jin, Z. D.
  193720. FUCHSB
  193721. JACSCeUNSATURATED SULFONE CONJUGATE ADDITION VINYL ENONE NOVEL ELIMINATION PHENYLSULFONYL CARBANION METHOXYM
  193722. 15059N
  193723. 2/28/96
  193724. SYNTHESES VIA VINYL SULFONES .52. A HIGHLY EFFICIENT SYNTHESIS OF b
  193725. SUBSTITUTED SIX
  193726.  and SEVEN
  193727. MEMBERED
  193728. RING ENONES VIA CARBON ALKYLATION OF g
  193729. METHOXY ALLYLSULFONYL ANIONS
  193730. 1994X    5995
  193731. 5996Y
  193732. 14051
  193733. EMANUEL, C. J.
  193734. JACSM
  193735. 15060N
  193736. 2/28/96
  193737. AyMECHANISM OF THE REACTION OF ATOMIC CARBON WITH PYRROLE. EVIDENCE FOR THE INTERMEDIACY OF A NOVEL DEHYDROPYRIDINIUM YLIDE
  193738. 1994X    5991
  193739. 5992Y
  193740. 14052
  193741. Lee, N. E.B
  193742. JACSM
  193743. 15061N
  193744. 2/28/96
  193745. AFASYMMETRIC HYDROGENATION OF ENAMINES WITH A CHIRAL TITANOCENE CATALYST
  193746. 1994X    5985
  193747. 5986Y
  193748. 14053
  193749. SHIBATA, K.
  193750. JACSM
  193751. 15062N
  193752. 2/28/96V
  193753. PERCHLOROTRIPHENYLENEW
  193754. 1994X    5983
  193755. 5984Y
  193756. 14054
  193757. IKEDA, S.
  193758. JACSCFALKYNE TIN ENONE NICKEL COUPLING CONJUGATE ADDITION MECHANISM CATALYSTM
  193759. 15063N
  193760. 2/28/96
  193761. AoSYNTHESIS OF STEREODEFINED ENYNES BY THE NICKEL
  193762. CATALYZED COUPLING REACTION OF ALKYNYLTINS, ALKYNES, and ENONES
  193763. 1994X    5975
  193764. 5976Y
  193765. 14055
  193766. AGGARWAL, V. K.
  193767. JACSM
  193768. 15064N
  193769. 2/28/96
  193770. NOVEL CATALYTIC CYCLE FOR THE SYNTHESIS OF EPOXIDES FROM ALDEHYDES and SULFUR YLIDES MEDIATED BY CATALYTIC QUANTITIES OF SULFIDES and RH2(OAC)4
  193771. 1994 X    5973
  193772. 5974Y
  193773. 14056
  193774. Wang, S. H.B
  193775. JACSM
  193776. 15065N
  193777. 2/28/96
  193778. A~MECHANISM OF OXIDATION OF TUNGSTEN h1
  193779. DIHYDROFUR
  193780. YL COMPOUNDS to h1
  193781. YL and FURTHER TO h1
  193782. BUTENOLIDE DERIVATIVES
  193783. 1994 X    5967
  193784. 5968Y
  193785. 14057
  193786. BAUSCH, M. J.
  193787. JACSM
  193788. 15066N
  193789. 2/28/96
  193790. AWEFFECTS OF A
  193791.  AND b
  193792. SILICON ATOMS ON THE FREE ENERGIES OF C
  193793. H HOMOLYSIS and HETEROLYSIS
  193794. 1994X    5963
  193795. 5964Y
  193796. 14058
  193797. GLUKHOVTSEV, M. N.
  193798. JACSM
  193799. 15067N
  193800. 2/28/96
  193801. AOIS SN2 SUBSTITUTION WITH INVERSION OF CONFIGURATION AT VINYLIC CARBON FEASIBLE?
  193802. 1994 X    5961
  193803. 5962Y
  193804. 14059
  193805. ADAM, W.
  193806. JACSCsTHERMAL
  193807. DECOMPOSITION 1,2
  193808. DIOXETANES MECHANISMS 3,3
  193809. DIBENZYL
  193810. DIOXETANE CHEMIEXCITATION PHOTOCHEMISTRY KINETICS M
  193811. 15068N
  193812. 2/28/96
  193813. THERMOLYSIS OF 3,3
  193814. BIS(PHENYLMETHYL)
  193815. DIOXETANE:  RADICAL
  193816. INDUCED FORMATION OF THE UNUSUAL DECOMPOSITION PRODUCT 3
  193817. PHENYL
  193818. (PHENYLMETHOXY)
  193819. PROPANONE
  193820. 1994 X    5674
  193821. 5678Y
  193822. 14060
  193823. KHUMTAVEEPORN, K.
  193824. ALPER 
  193825. JACSC
  193826. COBALT AZIRIDINES 
  193827. TRANSITION METAL CARBONYLATION HETEROCYCLE INSERTION CARBON MONOXIDE CO THIAZOLIDINE RHODIUM CATALYST CATALYSISM
  193828. 15069N
  193829. 2/28/96
  193830. A{SEQUENTIAL RING EXPANSION and KETENE ELIMINATION REACTIONS IN THE NOVEL RHODIUM(I)
  193831. CATALYZED CARBONYLATION OF THIAZOLIDINES
  193832. 1994 X    5662
  193833. 5666Y
  193834. 14061
  193835. VANDORT, P. C.
  193836. FUCHS
  193837. JACSC
  193838. ELIMINATIONS CYCLIZATION BOND 
  193839. SULFONE ELIMINATION WRITING INTRODUCTION SILICON ORTHO ACTIVATION SILYL FRIEDAL CRAFT SULFONYL PHENYLSULFONYL
  193840. 15070N
  193841. 2/28/96
  193842. SYNTHESIS VIA VINYL SULFONES .51. AMELIORATION OF THE LEAVING GROUP ABILITY OF THE ARYL SULFONE MOIETY VIA INTRAMOLECULAR OXYGEN SILYLATION
  193843. 1994 X    5657
  193844. 5661Y
  193845. 14062
  193846. BOGER, D. L.
  193847. JACSC
  193848. SELECTIVE SUBSTITUTION ACTIVATED BLEOMYCIN CARBOHYDRATE MOIETY D
  193849. MANNOSE DNA DERIVATIVES NEOCARZINOSTATIN DEGLYCOBLEOMYCIN PURIFICATION MECHANISMS M
  193850. 15071N
  193851. 2/28/96
  193852. TOTAL SYNTHESIS OF BLEOMYCIN A2 AND RELATED AGENTS .4. SYNTHESIS OF THE DISACCHARIDE SUBUNIT:  2
  193853. CARBAMOYL
  193854. MANNOPYRANOSYL)
  193855. GULOPYRANOSE and COMPLETION OF THE TOTAL SYNTHESIS OF BLEOMYCIN A2
  193856. 1994 X    5647
  193857. 5656Y
  193858. 14063
  193859. BOGER, D. L.
  193860. JACSC
  193861. DIELS
  193862. ALDER REACTIONS MAN
  193863. DESIGNED BLEOMYCINS METAL BINDING
  193864. SITE CARBAPENEM ANTIBIOTIC (+)
  193865. 5 ENOLATE IMINE CONDENSATION DNA
  193866. CLEAVING PROPERTIES BETA
  193867. AMINO ACID ASYMMETRIC
  193868. SYNTHESIS ALDOL REACTIONS ESTER ENOLATE M
  193869. 15072N
  193870. 2/28/96
  193871. TOTAL SYNTHESIS OF BLEOMYCIN A2 AND RELATED AGENTS .2. SYNTHESIS OF (
  193872. PYRIMIDOBLAMIC ACID, EPI
  193873. PYRIMIDOBLAMIC ACID, (+)
  193874. DESACETAMIDOPYRIMIDOBLAMIC ACID, and (
  193875. DESCARBOXAMIDOPYRIMIDOBLAMIC ACID
  193876. 1994 X    5619
  193877. 5630Y
  193878. 14064
  193879. KANDANARACHCHI, P.
  193880. JACSCTBASE CATALYSIS AQUEOUS
  193881. SOLUTION MECHANISM CARBOCATIONS LIFETIMES BREAKDOWN ALCOHOLS M
  193882. 15073N
  193883. 2/28/96
  193884. A{HYDROLYSIS OF ORTHOCARBONATES. EVIDENCE FOR CHARGE IMBALANCE IN THE TRANSITION STATE FOR THE GENERAL ACID CATALYZED PROCESS
  193885. 1994X    5601
  193886. 5606Y
  193887. 14065
  193888. A    ISEKI, K.
  193889. Chem. Lett.C#ASYMMETRIC
  193890. SYNTHESIS BORNANESULTAM M
  193891. 15074N
  193892. 2/28/96
  193893. REVERSAL OF STEREOSELECTIVITY IN THE ALDOL REACTION OF BORON ENOLATE DERIVED FROM OPPOLZER'S SULTAM WITH A,A
  193894. DIFLUORO and A,A,A
  193895. TRIFLUORO CARBONYL COMPOUNDS
  193896. 1994X    1135
  193897. 1138Z
  193898. 14066
  193899. YOKOYAMA, M.
  193900. Chem. Lett.M
  193901. 15075N
  193902. 2/28/96
  193903. A,THERMOLYSIS and PHOTOLYSIS OF SUGAR DIAZIDES
  193904. 1994 X    1107
  193905. 1110Z
  193906. 14067
  193907. FUNABIKI, K.
  193908. Chem. Lett.CPFLUOROOLEFIN DIPEPTIDE ISOSTERES STEREOSELECTIVE SYNTHESIS ESTERS KETONES ROUTE M
  193909. 15076N
  193910. 2/28/96
  193911. FLUORIDE ION
  193912. PROMOTED REACTION OF POLYFLUORO
  193913. PROPENYL P
  193914. TOLUENESULFONATE WITH AMINES. HIGHLY EFFICIENT and GENERAL ACCESS TO (Z)
  193915. FLUORO
  193916. AMINO ACRYLALDEHYDES
  193917. 1994 X    1075
  193918. 1078Z
  193919. 14068
  193920. NOKAMI, J.
  193921. Chem. Lett.CmHUMAN
  193922. IMMUNODEFICIENCY
  193923. VIRUS FACILE SYNTHESIS (
  193924. CARBOVIR ALKYLATION RESOLUTION ANALOGS MIMICS POTENT ROUTE M
  193925. 15077N
  193926. 2/28/96
  193927. PALLADIUM
  193928. CATALYZED CHEMOSELECTIVE REACTION OF ALLYLIC CARBONATE WITH NUCLEOSIDE BASES and ITS APPLICATION FOR THE SYNTHESIS OF CARBOCYCLIC NUCLEOSIDES. (
  193929.  and (+)
  193930. CARBOVIRS
  193931. 1994X    1071
  193932. 1074Z
  193933. 14069
  193934. MAEKAWA, H.
  193935. Chem. Lett.CBDOUBLE MEDIATORY SYSTEM INDIRECT ELECTROOXIDATION ALCOHOLS ESTERS M
  193936. 15078N
  193937. 2/28/96
  193938. AJFACILE SYNTHESIS OF A
  193939. KETO CARBONYL COMPOUNDS BY INDIRECT ANODIC OXIDATION
  193940. 1994 X    1017
  193941. 1020Z
  193942. 14070
  193943. A    HONDA, T.
  193944. Chem. Lett.C-ME3SISNBU3 ROUTE CYCLOPENTANONES EQUIVALENTS M
  193945. 15079N
  193946. 2/28/96
  193947. NOVEL CYCLIZATION REACTION BY TANDEM MICHAEL ADDITION 
  193948. DIECKMANN CONDENSATION USING STANNYL ANION GENERATED FROM BU3SNSIME3 and F
  193949. 1994X    1013
  193950. 1016Z
  193951. 14071
  193952. FUKUHARA, T.
  193953. Chem. Lett.C
  193954. DIAZOTIZATION BASE M
  193955. 15080N
  193956. 2/28/96
  193957. FACILE PREPARATION OF AROMATIC FLUORIDES BY THE FLUORO
  193958. DEDIAZONIATION OF AROMATIC DIAZONIUM TETRAFLUOROBORATES USING HF
  193959. PYRIDINE SOLUTION
  193960. 1994 X    1011
  193961. 1012Z
  193962. 14072
  193963. FURUKAWA, N.
  193964. Chem. Lett.
  193965. SELENIUM PARTICIPATION MOLECULAR
  193966. OXYGEN ANODIC
  193967. OXIDATION 1,8
  193968. BIS(METHYLSELENO)NAPHTHALENE 1,5
  193969. DITHIACYCLOOCTANE DETHIOACETALIZATION PHOTOOXIDATION 1,3
  193970. DITHIANES DITHIOACETALS DERIVATIVES M
  193971. 15081N
  193972. 2/28/96
  193973. AvTHE SIMPLE PREPARATION OF ALDEHYDES and KETONES BY THE PHOTO
  193974. OXYGEN REARRANGEMENT OF NAPHTHO[1,8
  193975. DE]DITHIIN MONOOXIDES
  193976. 1994 X    1007
  193977. 1010Z
  193978. 14073
  193979. LUTZ, T. G.
  193980. Can. J. Chem.Ce0.6 M NA(CL) AQUEOUS
  193981. SOLUTION EQUILIBRIUM SILICON(IV) ACID 3
  193982. HYDROXY
  193983. PYRIDINONES INDIUM HYDROLYSIS M
  193984. 15082N
  193985. 2/28/96
  193986. PREPARATION OF 2
  193987.  AND 4
  193988. SUBSTITUTED 3
  193989. HYDROXY
  193990. METHYLFURANS and THE ALUMINUM AND GALLIUM COMPLEXES OF 3
  193991. HYDROXY
  193992. METHYL
  193993. METHYLFORMAMIDO)FURAN
  193994. 1994 X    1362
  193995. 1369Y
  193996. 14074
  193997. CULLEN, W. R.
  193998. Can. J. Chem.C
  193999. BINUCLEAR DIRHODIUM COMPOUNDS ORTHO
  194000. METALATION REACTIONS RH
  194001. RH BOND MOLECULAR
  194002. STRUCTURE ELECTRONIC
  194003. STRUCTURE COMPLEXES LIGANDS PHOSPHINES CATALYSTS CRYSTAL M
  194004. 15083N
  194005. 2/28/96
  194006. ANCHARACTERIZATION and NONRIGID BEHAVIOUR OF A CARBOXYLATE
  194007. BRIDGED RHODIUM DIMER
  194008. 1994 X    1294
  194009. 1301Y
  194010. 14075
  194011. MUKERJEE, A. K.
  194012. Can. J. Chem.M
  194013. 15084N
  194014. 2/28/96
  194015. AOREACTION OF UNSATURATED AZLACTONES WITH SULFUR NUCLEOPHILES:  SOME OBSERVATIONS
  194016. 1994X    1383
  194017. 1387Y
  194018. 14076
  194019. AKSSIRA, M.
  194020. Can. J. Chem.C)ALLYLAMINES ACID AMINATION ESTERS AMINES M
  194021. 15085N
  194022. 2/28/96
  194023. SYNTHESIS OF DIALLYLAMINES and TRIALLYLAMINES FROM 3
  194024. ACETOXY
  194025. METHYLENE PROPIONITRILES and METHYL 3
  194026. ACETOXY
  194027. METHYLENE PROPIONATES
  194028. 1994 X    1357
  194029. 1361Y
  194030. 14077
  194031. A    LOUIS, C.
  194032. Can. J. Chem.C
  194033. REACTIVITY NITRONES M
  194034. 15086N
  194035. 2/28/96
  194036. AfSYNTHESIS OF ENANTIOMERIC b
  194037. AMINO KETONES VIA 1,3
  194038. DIPOLAR CYCLOADDITION and CHROMATOGRAPHIC RESOLUTION
  194039. 1994X    1347
  194040. 1350Y
  194041. 14078
  194042. FRIESEN, R. W.
  194043. Can. J. Chem.C
  194044. TRIBUTYLSTANNYL GLYCALS ORGANIC ELECTROPHILES MOLECULAR
  194045. STRUCTURE ORGANOTIN REAGENTS OXIDATIVE ADDITION SYNTHETIC ROUTE PAPULACANDIN
  194046. B TIN REAGENTS HALIDES CHAETIACANDIN M
  194047. 15087N
  194048. 2/28/96
  194049. APTHE PREPARATION OF C
  194050. ARYL GLUCALS VIA PALLADIUM
  194051. CATALYZED CROSS
  194052. COUPLING METHODS
  194053. 1994 X    1262
  194054. 1272Y
  194055. 14079
  194056. Liu, H. J.B
  194057. Can. J. Chem.C
  194058. CHIRAL TITANIUM REAGENT CATALYZED ENE REACTIONS STEREOCHEMICAL ASPECTS CONVERSION ALDEHYDES NOPINONE DIENE ROUTE CYCLOCONDENSATION (
  194059. PINENE M
  194060. 15088N
  194061. 2/28/96
  194062. FACIAL SELECTIVE DIELS
  194063. ALDER REACTIONS OF (1R,5R)
  194064. CARBOMETHOXY
  194065. DIMETHYL BICYCLO[3.1.1]HEPT
  194066. ONE. UNUSUAL KETALIZATION
  194067. FRAGMENTATION REACTION OF ADDUCTS
  194068. 1994 
  194069. tX    1193
  194070. 1210Y
  194071. 14080
  194072. CHAN, T. H.
  194073. Can. J. Chem.C
  194074. POT SYNTHESIS CARBONYL
  194075. COMPOUNDS ACID KDN PD(0)
  194076. CATALYZED CYCLIZATION FACILE SYNTHESIS BOND FORMATION ALPHA
  194077. ALKOXY INDIUM ALDEHYDES METHYLENETETRAHYDROFURANS M
  194078. 15089N
  194079. 2/28/96
  194080. Ax1993 R. U. LEMIEUX AWARD LECTURE 
  194081.  ORGANOMETALLIC
  194082. TYPE REACTIONS IN AQUEOUS MEDIA 
  194083.  A NEW CHALLENGE IN ORGANIC SYNTHESIS
  194084. 1994 X    1181
  194085. 1192Y
  194086. 14081
  194087. ANDERSSON, P. G.
  194088. Tet. Lett.C
  194089. STEREOCONTROLLED LACTONIZATION REACTIONS CONJUGATED DIENES (PI
  194090. ALLYL)PALLADIUM COMPLEXES CATALYZED 1,4
  194091. ADDITION PRESSURE CARBONYLATION ESTERS 
  194092. A NEW PALLADIUM
  194093. MEDIATED TANDEM CYCLIZATION
  194094. CARBONYLATION OF 1,3
  194095. DIENES IS DESCRIBED. THE REACTION PROCEEDS VIA AN INTRAMOLECULAR NUCLEOPHILIC ADDITION ON THE DIENE TO GIVE AN INTERMEDIATE PI
  194096. ALLYL PALLADIUM COMPLEX WHICH IS SUBSEQUENTLY CARBONYLATED TO GIVE EITHER A OVERALL 1,2
  194097.  OR 1,4
  194098. ADDITION OVER THE DIENE. BY PROPER CHOICE OF REACTION CONDITIONS CONTROL OF THE REGIOCHEMICAL OUTCOME OF THE REACTION WAS OBTAINED.
  194099. 15090N
  194100. 2/28/96
  194101. A]PALLADIUM
  194102. MEDIATED STEREO
  194103.  and REGIOSELECTIVE TANDEM
  194104. CYCLIZATION
  194105. CARBONYLATIONS OF 1,3
  194106. DIENES
  194107. 1994 X    4441
  194108. 4444Y
  194109. 14082
  194110. CATENA, J.
  194111. BOSCH
  194112. Tet. Lett.CzSTRYCHNOS ALKALOIDS INDOLE ALKALOIDS ENTRY 
  194113.  PUMMERER CYCLIZATION SULFOXIDE HETEROCYCLE ALKALOID INDOLE INTRODUCTION AMINO
  194114. 'PUMMERER CYCLIZATION OF BETA
  194115. AMINOETHYL SULFOXIDE 6 WAS EFFECTIVELY ACHIEVED USING TFAA
  194116. TFA IN TOLUENE AT 80 DEGREES C. THE CYCLIZED PRODUCT 7 WAS THEN CONVERTED TO THE ALKALOID DEETHYLIBOPHYLLIDINE. THE REQUIRED PYRROLO[3,2
  194117. C]CARBAZOLE 6 WAS PREPARED IN FIVE STEPS FROM 4
  194118. METHOXYPHENETHYLAMINE.
  194119. 15091N
  194120. 2/28/96
  194121. AlTHE PUMMERER CYCLIZATION ROUTE to THE IBOPHYLLIDINE ALKALOIDS. TOTAL SYNTHESIS OF (+/
  194122. DEETHYLIBOPHYLLIDINE
  194123. 1994X    4433
  194124. 4436Y
  194125. 14083
  194126. A    GRIGG, R.
  194127. Tet. Lett.
  194128. xCOSTEREOSPECIFIC GROUP TRANSFER HYDRIDE ION CAPTURE CASCADE CYCLIZATION REAGENTS 
  194129. MA SERIES OF PALLADIUM CATALYSED THREE COMPONENT CYCLISATION
  194130. CARBONYLATION
  194131. ANION CAPTURE PROCESSES INVOLVING ARYL IODIDES, CARBON MONOXIDE (1 ATM) AND SN(IV)R OR B(III)R REAGENTS ARE REPORTED. THE STEREO
  194132.  AND REGIO
  194133. SPECIFIC CASCADE PROCESSES FURNISH TETRASUBSTITUTED CARBON CENTRES AND FUSED
  194134.  AND SPIROCYCLIC
  194135. RINGS IN EXCELLENT YIELD.
  194136. 15092N
  194137. 2/28/96
  194138. AVTHREE COMPONENT PALLADIUM CATALYSED CYCLISATION
  194139. CARBONYLATION
  194140. ANION  CAPTURE PROCESSES
  194141. 1994 X    4429
  194142. 4432Y
  194143. 14084
  194144. O'DONOVAN, A. R. M.
  194145. Tet. Lett.C
  194146. DERIVATIVES 
  194147. METHODS OF PREPARATION OF THE FOUR BIS(TRIMETHYLSILYL)THIOPHENE ISOMERS AND 2,3,5
  194148. TRIS(TRIMETHYLSILYL)THIOPHENE ARE DESCRIBED;  THE CORRESPONDING DIOXIDES ARE VERSATILE INTERMEDIATES FOR THE DIELS
  194149. ALDER REACTION.M
  194150. 15093N
  194151. 2/28/96
  194152. AKPREPARATION and CYCLOADDITION REACTIONS OF SILYLATED THIOPHENE 1,1
  194153. DIOXIDES
  194154. 1994 X    4425
  194155. 4428Y
  194156. 14085
  194157. SEERDEN, J. P. G.
  194158. SCHEERNB
  194159. Tet. Lett.C
  194160. 2 CYCLO
  194161. ADDITIONS CARBONYL
  194162. COMPOUNDS ALKENES STEREOCONTROL CHEMISTRY ACIDS ALPHA 
  194163.  NITRONE DIPOLAR CYCLOADDITION CHIRAL ASYMMETRIC KETENE ACETAL BORON LEWIS ACID CATALYST INDUCTION
  194164. ASYMETRIC 1,3
  194165. DIPOLAR CYCLOADDITION OF NITRONES WITH KETENE ACETALS IS STRONGLY CATALYZED BY CHIRAL OXAZABOROLIDINES DERIVED FROM N
  194166. TOSYL
  194167. ALPHA
  194168. AMINO ACIDS. THE 5,5
  194169. DIALKOXYISOXAZOLIDINES ARE OBTAINED REGIOSELECTIVELY IN HIGH YIELD WITH HIGH STEREOSELECTIVITY AND MODERATE ENANTIOSELECTIVITY ICP TO 62% EE. MILD HYDROGENOLYSIS OF THE N
  194170. O BOND YIELDS QUANTITATIVELY THE CORRESPONDING BETA
  194171. AMINO
  194172. ESTER.
  194173. 15094N
  194174. 2/28/96
  194175. AiASYMMETRIC 1,3
  194176. DIPOLAR CYCLOADDITION OF NITRONES WITH KETENE ACETALS CATALYZED BY CHIRAL OXAZABOROLIDINES
  194177. 1994 X    4419
  194178. 4422Y
  194179. 14086
  194180. JACKSON, R. F. W.
  194181. Tet. Lett.C
  194182. ANTIBIOTICS 
  194183. REACTION OF THE L
  194184. SERINE DERIVED ZINC REAGENT 3 WITH ACRYLOYL CHLORIDE GAVE THE 4
  194185. OXO AMINO ACID 4, WITH NO EVIDENCE OF PRODUCTS ARISING FROM CONJUGATE ADDITION. TREATMENT OF THE ADDUCT 4 WITH BENZYLAMINE GAVE PROTECTED 4
  194186. OXOLYSINE 5 DIRECTLY. REDUCTION OF THE KETONE PROCEEDED WITHOUT SIGNIFICANT STEREOSELECTIVITY TO GIVE THE 4
  194187. HYDROXYLYSINE DERIVATIVES 6 AS A DIASTEREOISOMERIC MIXTURE. TREATMENT OF THE ADDUCT 4 WITH HCL/ETHER GAVE 4
  194188. OXOPIPECOLIC ACID BENZYL ESTER HYDROCHLORIDE 7 IN QUANTIB3TATIVE YIELD. EVIDENCE FOR INITIAL FORMATION OF THE
  194189. 15095N
  194190. 2/28/96
  194191. AgSYNTHESIS OF PROTECTED 4
  194192. OXOPIPECOLIC ACID and 4
  194193. OXOLYSINE USING A PALLADIUM
  194194. CATALYSED COUPLING PROCESS
  194195. 1994 X    4417
  194196. 4418Y
  194197. 14087
  194198. SUCHETA, K.
  194199. Tet. Lett.C.ESTERIFICATION MACROLIDES ACTIVATION LACTONES K
  194200. CARBOXYLIC ACIDS WERE CONVENIENTLY ESTERFIED WITH ALCOHOLS AND THIOLS BY THE USE OF TRIPHENYLPHOSPHINE AND N
  194201. BROMO/IODO SUCCINIMIDE TO AFFORD THE CORRESPONDING ESTERS AND THIOL ESTERS.M
  194202. 15096N
  194203. 2/28/96
  194204. AONOVEL, GENERAL ROUTE to THE SYNTHESIS OF CARBOXYLIC ACID ESTERS and THIOLESTERS
  194205. 1994 X    4415
  194206. 4416Y
  194207. 14088
  194208. NYERGES, M.
  194209. TOKEB
  194210. Tet. Lett.C^ANALOGS 
  194211.  DIPOLAR CYCLOADDITION AZOMETHINE YLIDE ALKALOID TARGET CEPHALOTAXINE PICTET SPENGLER
  194212. THE AZA
  194213. ANALOGUE OF CEPHALOTAXINE SKELETON HAS BEEN PREPARED BY SERIES OF REACTIONS WHICH INCLUDE A 1,3
  194214. DIPOLAR CYCLOADDITION IN 100 % DIASTEREOSELECTIVITY.M
  194215. 15097N
  194216. 2/28/96
  194217. Ah1,3
  194218. DIPOLAR CYCLOADDITION APPROACH TOWARDS THE STEREOSELECTIVE PREPARATION OF AZA
  194219. CEPHALOTAXINE SKELETON
  194220. 1994X    4413
  194221. 4414Y
  194222. 14089
  194223. BROWN, R. F. C.
  194224. Tet. Lett.C
  194225. ANHYDRIDE 
  194226. !CYCLOPENT[A]INDENE (BENZOPENTALENE, 7) IS GENERATED BY FLASH VACUUM PYROLYSIS OF 3
  194227. PHENYLPHTHALIC ANHYDRIDE (6), BIPHENYLENE (3) OR DIPHENIC ANHYDRIDE (4). IT DIMERISES READILY AND ADDS CYCLOPENTADIENE ABOVE 
  194228. 70 DEGREES C, BUT IT DOES NOT EQUILIBRATE AT 900 DEGREES C WITH AS
  194229. INDACENE (1).
  194230. 15098N
  194231. 2/28/96
  194232. AgCYCLOPENT[A]INDENE (BENZOPENTALENE):  GENERATION BY FLASH VACUUM PYROLYSIS and SUBSEQUENT DIMERISATION.
  194233. 1994X    4405
  194234. 4408Y
  194235. 14090
  194236. MIYAZAKI, Y.
  194237. Tet. Lett.C[ASYMMETRIC DIHYDROXYLATION STEREOSPECIFIC SYNTHESIS ALLYLSILANES ALKYLATION PHEROMONE ACID 
  194238. .A NEW CHIRAL BUILDING BLOCK BETA
  194239. HYDROXY
  194240. GAMMA
  194241. TRIMETHYLSILYL
  194242. GAMMA
  194243. BUTYROLACTONE (1) WAS PREPARED FROM GAMMA
  194244. TRIMETHYLSILYLALLYL ACETATE (2) VIA TWO STEPS IN EXCELLENT OVERALL YIELD. THE LACTONE 1 IS USEFUL PRECURSOR TO FOUR
  194245. CARBON CHAIN BLOCKS HAVING TERTIARY STEREOGENIC CENTER SUCH AS 6, 10 AND 11.
  194246. 15099N
  194247. 2/28/96
  194248. SYNTHESIS OF b
  194249. HYDROXY
  194250. TRIMETHYLSILYL
  194251. BUTYROLACTONE AS KEY CHIRAL BUILDING BLOCK FOR PREPARATION OF FOUR
  194252. CARBON CHAIN UNITS HAVING TERTIARY STEREOGENIC CARBON
  194253. 1994 X    4389
  194254. 4392Y
  194255. 14091
  194256. UYEO, S.
  194257. Tet. Lett.C4ANTIBACTERIAL ACTIVITY PENEM ANTIBIOTICS CARBAPENEM 
  194258. REACTION OF ACETOXY
  194259. AZETIDINONE 4, (Z)
  194260. CROTYLBROMIDE 5 AND ZN SELECTIVELY GAVE 6, WHICH WAS CONVENED TO 1 BETA
  194261. METHYL
  194262. (HYDROXYMETHYL)CARBAPENEM 11, A KEY INTERMEDIATE IN SYNTHESIS OF ANTIBIOTIC 2, IN HIGH OVERALL YIELD.M
  194263. 15100N
  194264. 2/28/96
  194265. AVPRACTICAL, STEREOCONTROLLED SYNTHESIS OF 2
  194266. FUNCTIONALIZED
  194267. METHYL
  194268. METHYLCARBAPENEMS
  194269. 1994 X    4377
  194270. 4378Y
  194271. 14092
  194272. HATAKEYAMA, S.
  194273. Tet. Lett.CFHYDROXYL FUNCTIONS ORGANIC
  194274. SYNTHESIS TRIETHYLSILANE PROTECTION ETHERS K
  194275. AN EFFICIENT TMSOTF CATALYZED ETHER SYNTHESIS FROM CARBONYL COMPOUNDS AND ALKOXYTRIMETHYLSILANES VIA TRIETHYLSILANE
  194276. REDUCTION IS DESCRIBED.M
  194277. 15101N
  194278. 2/28/96
  194279. ATEFFICIENT REDUCTIVE ETHERIFICATION OF CARBONYL COMPOUNDS WITH ALKOXYTRIMETHYLSILANES
  194280. 1994X    4367
  194281. 4370Y
  194282. 14093
  194283. CHUANG, C. P.
  194284. Tet. Lett.C}ORTHO METALATION REACTIONS ORGANIC
  194285. SYNTHESIS CHAIN REACTIONS OCHROMYCINONE CYCLIZATION X
  194286. 14881 MN(III) OLEFINS DESIGN CE(IV) K
  194287. THE MANGANESE(III) INITIATED OXIDATIVE FREE RADICAL REACTION BETWEEN 1,4
  194288. NAPHTHOQUINONE AND ALPHA
  194289. BENZYL MALONATES GIVING BENZO[1]ANTHRAQUINONES IS DESCRIBED.M
  194290. 15102N
  194291. 2/28/96
  194292. AqMANGANESE(III) ACETATE INITIATED OXIDATIVE FREE RADICAL REACTION BETWEEN 1,4
  194293. NAPHTHOQUINONE and A
  194294. BENZYLMALONATES
  194295. 1994X    4365
  194296. 4366Y
  194297. 14094
  194298. BEUGELMANS, R.
  194299. Tet. Lett.C#TRIBUTYLTIN HYDRIDE CLEAVAGE ACIDS K
  194300. TREATMENT OF ARYL ALLYL ETHERS WITH CATALYTIC AMOUNTS OF PD(PPH(3))(4) AND NABH4 AT ROOM TEMPERATURE AFFORDED THE PARENT PHENOL IN HIGH YIELD UNDER NON
  194301. HYDROLYTIC CONDITIONS.M
  194302. 15103N
  194303. 2/28/96
  194304. A@REDUCTIVE DEPROTECTION OF ARYL ALLYL ETHERS WITH PD(PPH3)4/NABH4
  194305. 1994 X    4349
  194306. 4350Y
  194307. 14095
  194308. HARTENSTEIN, H.
  194309. Tet. Lett.CALIQUID
  194310. CHROMATOGRAPHY CONVENIENT SYNTHESIS DECOMPOSITION ANALOGS K
  194311. NATURALLY OCCURRING HEMIACETALS DIBOA AND DIMBOA WERE SYNTHESIZED BY THE FIRST ALPHA
  194312. HYDROXYLATION OF N
  194313. HYDROXYLACTAMS VIA M
  194314. CHLOROPERBENZOIC ACID OXIDATION OF CORRESPONDING CYCLOSILYL ENOL ETHERS.M
  194315. 15104
  194316. 2/28/96
  194317. HYDROXYLATION OF CYCLIC HYDROXAMIC ACIDS BY PEROXIDE OXIDATION:  A NOVEL APPROACH to ALLELOCHEMICALS FROM GRAMINEAE
  194318. 1994X    4335
  194319. 4338Y
  194320. 14096
  194321. ADAM, W.
  194322. Tet. Lett.C
  194323. DIELS
  194324. ALDER REACTIONS ENE REACTION DIASTEREOFACIAL SELECTIVITY ALLYLIC SUBSTITUENTS FACIAL SELECTIVITY PHOTOOXYGENATION ADDITIONS ALCOHOLS DIENES 
  194325. FROM 1
  194326. BROMO
  194327. METHYLNAPHTHALENE EIGHT CHIRAL DERIVATIVES 1 WITH A VARIETY OF FUNCTIONAL GROUPS AT THE STEREOGENIC CENTER WERE PREPARED, WHICH WITH SINGLET OXYGEN LED TO THE CORRESPONDING ENDOPEROXIDES 2 IN SUBSTITUENT
  194328. DEPENDENT PI
  194329. FACIAL SELECTIVITY OF STEREOELECTRONIC ORIGIN.
  194330. 15105N
  194331. 2/28/96
  194332. AwSUBSTITUENT EFFECTS IN THE DIASTEREOSELECTIVE [4+2] CYCLOADDITION OF CHIRAL NAPHTHALENE DERIVATIVES WITH SINGLET OXYGEN
  194333. 1994 X    4331
  194334. 4334Y
  194335. 14097
  194336. DENMARK, S. E.
  194337. Tet. Lett.C
  194338. ALDOL CONDENSATION TRIARYLCARBENIUM IONS DIASTEREOSELECTIVE SILYL ENOL ETHERS TRITYL PERCHLORATE CONVENIENT METHOD ACETALS ALDEHYDES 
  194339. PHENYL
  194340. 2: 3,6: 7
  194341. DIBENZOSUBERYL SALTS 5(+) EFFICIENTLY CATALYZE THE ALDOL REACTION BETWEEN SILYL ENOL ETHERS AND BENZALDEHYDE WITH MODERATE DIASTEREOSELECTIVITY. CROSSOVER EXPERIMENTS WITH DOUBLY LABELED SILYL ENOL ETHERS, KINETIC AND STEREOCHEMICAL STUDIES IDENTIFY 5(+) AS THE CATALYST RATHER THAN A LEWIS ACIDIC R(3)SIX SPECIES IN THIS TRANSFORMATION.
  194342. 15106N
  194343. 2/28/96
  194344. A`TRIARYLCARBENIUM IONS AS CATALYSTS IN THE MUKAIYAMA ALDOL ADDITION:  A MECHANISTIC INVESTIGATION
  194345. 1994 X    4327
  194346. 4330Y
  194347. 14098
  194348. CARREIRA, E. M.
  194349. Tet. Lett.
  194350. A MECHANISTIC STUDY OF THE MUKAIYAMA ALDOL ADDITION REACTION EMPLOYING BENZALDEHYDE AND HYDROCINNAMALDEHYDE ALONG WITH A SELECTION OF LEWIS ACIDS INCLUDING BF3.OET(2), LICLO4, YB(OTF)(3), SN(OTF)(2), AND ZN(OTF)(2) IS PRESENTED. THE RESULTS OF EXPERIMENTS CONDUCTED WITH DOUBLY
  194351. LABELED SILYL KETENE ACETALS IMPLICATE A LEWIS ACIDIC SILICON SPECIES AND NOT THE METALS AS THE CATALYST IN THE MUKAIYAMA ALDOL ADDITION REACTION.
  194352. 15107N
  194353. 2/28/96
  194354. ANMETAL VERSUS SILYL TRIFLATE CATALYSIS IN THE MUKAIYAMA ALDOL ADDITION REACTION
  194355. 1994 X    4323
  194356. 4326Y
  194357. 14099
  194358. Qiu, Z. M.B
  194359. Tet. Lett.C
  194360. INHIBITORS PROTEASE 
  194361. YBETA
  194362. FLUOROPYRROLE DERIVATIVES ARE SYNTHESIZED IN HIGH YIELDS BY THE REACTION OF ALPHA,ALPHA
  194363. DIFLUORO
  194364. GAMMA
  194365. GAMMA
  194366. (ELECTRON
  194367. WITHDRAWING
  194368. GROUP)
  194369. SUBSTITUTED KETONES AND AMMONIUM HYDROXIDE AT ROOM TEMPERATURE;  PROVIDING A NEW, SIMPLE, AND EFFICIENT METHOD FOR THE SYNTHESIS OF BETA
  194370. FLUORINATED PYRROLE RINGS. A POSSIBLE MECHANISM IS PROPOSED.
  194371. 15108N
  194372. 2/28/96
  194373. A>A NEW APPROACH to THE SYNTHESIS OF b
  194374. FLUOROPYRROLE DERIVATIVES
  194375. 1994 X    4319
  194376. 4322Y
  194377. 14100
  194378. HABI, A.
  194379. Tet. Lett.C$REARRANGEMENT SUBSTITUENT ALKOXIDES 
  194380. sTHE EFFICIENT AND RAPID ALPHA TO GAMMA REARRANGEMENT OF THE CARBALKOXY GROUP IN ALPHA
  194381. DISUBSTITUTED BETA
  194382. KETOESTERS IS REPORTED. THE REACTION PROCEEDS AT ROOM TEMPERATURE AND IN HIGH YIELDS WHEN PERFORMED UNDER NAKED ANION CONDITIONS. A CROSSOVER EXPERIMENT USING APPROPRIATELY SUBSTITUTED BETA
  194383. KETOESTERS IS CONSISTENT WITH A CYCLOBUTANEDIONE MONOHEMIKETAL INTERMEDIATE.
  194384. 15109N
  194385. 2/28/96
  194386. EFFICIENT 1,3 ESTER SHIFT IN A
  194387. DISUBSTITUTED b
  194388. KETOESTER ENOLATES, REMARKABLE INFLUENCE OF THE METAL COUNTERION ON THE RATE OF REACTION
  194389. X    4315
  194390. 4318Y
  194391. 14101
  194392. BARTON, D. H. R.
  194393. Tet. Lett.C)SATURATED
  194394. HYDROCARBONS FUNCTIONALIZATION K
  194395. OXIDATION OF ALLYLIC METHYLENE GROUPS UNDER FE
  194396. TBHP (FE
  194397. BUTYL HYDROPEROXIDE) AND FE
  194398. PA (FE
  194399. BUTYL HYDROPEROXIDE
  194400. PICOLINIC ACID) CONDITIONS GAVE ALPHA
  194401.  AND GAMMA
  194402. KETONIZATION PRODUCTS.M
  194403. 15110N
  194404. 2/28/96
  194405. AUOXIDATION OF ALLYLIC METHYLENE GROUPS UNDER FE
  194406. TBHP and FE
  194407. PA CONDITIONS
  194408. 1994 X    4307
  194409. 4310Y
  194410. 14102
  194411. PASTO, D. J.
  194412. Tet. Lett.C    EPOXIDES 
  194413. WTHE SYNTHETIC UTILITY OF THE GENERATION AND STUDY OF THE REACTIONS OF ALKOXY RADICALS GENERATED BY THE PHOTO
  194414. INDUCED, HOMOLYTIC DISSOCIATION OF ALKYL 4
  194415. NITROBENZENE SULFENATES IS DEMONSTRATED. THE EFFICIENT FORMATION OF REMOTELY SUBSTITUTED ALCOHOL DERIVATIVES, AND THE ADDITION OF THE ALKOXY RADICAL TO A REMOTELY SITUATED C=C IS ILLUSTRATED.
  194416. 15111N
  194417. 2/28/96
  194418. DEMONSTRATION OF THE SYNTHETIC UTILITY OF THE GENERATION OF ALKOXY RADICALS BY THE PHOTO
  194419. INDUCED, HOMOLYTIC DISSOCIATION OF ALKYL 4
  194420. NITROBENZENESULFENATES
  194421. 1994X    4303
  194422. 4306Y
  194423. 14103
  194424. NYLUND, C. S.
  194425. Tet. Lett.C
  194426. PALLADIUM
  194427. CATALYZED VINYLATION PHASE
  194428. TRANSFER CONDITIONS ALLYLIC ALKYLATION ORGANIC HALIDES CYCLIZATIONS REGIOSELECTIVITY COMPLEXES OLEFINS IODIDES 
  194429. >TWO C
  194430. C BONDS ARE READILY FORMED BY NUCLEOPHILIC ADDITION OF STABILIZED CARBANIONS TO THE PI
  194431. ALLYLPALLADIUM INTERMEDIATE REGIOSELECTIVELY PRODUCED BY THE HECK REACTION OF A VINYL BROMIDE AND AN UNACTIVATED OLEFIN. AN INTRAMOLECULAR VERSION OF THIS CONDENSATION GIVES FUNCTIONALIZED CARBOBICYCLIC COMPOUNDS AS PRODUCTS.
  194432. 15112N
  194433. 2/28/96
  194434. A^CONSECUTIVE CARBON
  194435. CARBON BOND FORMATION VIA THE p
  194436. ALLYLPALLADIUM VARIANT OF THE HECK REACTION
  194437. 1994 X    4287
  194438. 4290Y
  194439. 14104
  194440. KAMENECKA, T. M.
  194441. Tet. Lett.C
  194442. DIELS
  194443. ALDER APPROACH FUNCTIONALIZED CIS
  194444. HYDROISOQUINOLINES CARBONYL
  194445. COMPOUNDS TRICYCLIC HEART ALKALOIDS SPONGE ALDEHYDES KETONES CORE SUBSTRUCTURE K
  194446. A NEW APPROACH FOR ASYMMETRIC CONSTRUCTION OF THE PYRROLO[2,3
  194447. ISOQUINOLINE CORE OF MANZAMINE A IS DESCRIBED. THE SYNTHESIS STARTS WITH D
  194448. QUINIC ACID AND FEATURES AN INTRAMOLECULAR MANNICH REACTION AS THE CENTRAL STEP.M
  194449. 15113N
  194450. 2/28/96
  194451. A<AN ENANTIOSELECTIVE APPROACH to THE SYNTHESIS OF MANZAMINE A
  194452. 1994 X    4279
  194453. 4282Y
  194454. 14105
  194455. MOKHALLALATI, M. K.
  194456. Tet. Lett.
  194457. C]ASYMMETRIC TANDEM ADDITIONS CHIRAL NAPHTHYLOXAZOLINES NAPHTHALENES OXAZOLINES AUXILIARY RING 
  194458. YA DIASTEREOSELECTIVE ADDITION OF GRIGNARD REAGENTS TO NONRACEMIC 2
  194459. NAPHTHYL)
  194460.  (4R)
  194461.  PHENYL
  194462. OXAZOLIDINES (1) FOLLOWED BY ELECTROPHILIC TRAPPING OF THE AZAENOLATE IS DESCRIBED. THIS TANDEM ADDITION WAS PERFORMED IN A SINGLE FLASK PRODUCING, 1,1,2
  194463. TRISUBSTITUTED 1,2
  194464. DIHYDRONAPHTHALENES 7 IN EXCELLENT YIELDS AND HIGH ENANTIOSELECTIVITIES.
  194465. 15114N
  194466. 2/28/96
  194467. AbA SINGLE
  194468. POT SYNTHESIS OF 1,1,2
  194469. TRISUBSTITUTED 1,2
  194470. DIHYDRONAPHTHALENES IN HIGH ENANTIOMERIC PURITY
  194471. 1994 X    4267
  194472. 4270Y
  194473. 14106
  194474. Gil, J. F.B
  194475. Tetrahedron
  194476. NAPHTHALENE
  194477. CATALYZED LITHIATION SYNTHETIC APPLICATIONS BARBIER
  194478. TYPE 4,4'
  194479. BUTYLBIPHENYL
  194480. CATALYZED LITHIATION CARBONYL
  194481. COMPOUNDS LITHIUM ROUTE TETRAHYDROFURAN REACTIVITY ETHERS 
  194482. THE REACTION OF ACYCLIC 1,6
  194483. DIOL 11A WITH 85% PHOSPHORIC ACID AT TOLUENE REFLUX YIELDS KETONE 13A THROUGH AN INTRAMOLECULAR 1,6
  194484. HYDRIDE TRANSFER. THIS FACT IS PROVEN BY USING A DEUTERATED 1,6
  194485. DIOL (19), IN WHICH THE CORRESPONDING 1,6
  194486. DEUTERIDE TRANSFER OCCURS. A MECHANISTIC PROPOSAL THROUGH A PROTONATED OXEPANE (II) IS FORMULATED, WHICH IMPLIES AN ACTUAL 1,3
  194487. HYDRIDE TRANSFER;  THIS MECHANISM DIFFERS FROM THE REPORTED ONE IN THE LITERATURE FOR CYCLIC 1,6
  194488. DIOLS, IN WHICH A REAL 1,6
  194489. HYDRIDE TB.RANSFER TAKES PLACE DUE TO A PROXIMITY EFFECT.
  194490. 15115N
  194491. 2/28/96
  194492. ANINTRAMOLECULAR 1,6
  194493. HYDRIDE TRANSFER IN ACYCLIC 1,6
  194494. DIOLS:  A MECHANISTIC STUDY
  194495. 1994 X    7307
  194496. 7314Y
  194497. 14107
  194498. IRANPOOR, N.
  194499. TetrahedronCCSULFONIC
  194500. CARBOXYLIC ANHYDRIDES AMMONIUM
  194501. NITRATE MILD EPOXIDES ACID 
  194502. _THE REACTION OF CERIUM(IV) AS CERIC AMMONIUM NITRATE (CAN) WITH A VARIETY OF ALLYLIC AND TERTIARY BENZYLIC ETHERS AND ESTERS HAS BEEN EXAMINED IN DIFFERENT ALCOHOLS AND ACETIC ACID UNDER CATALYTIC AND MILD CONDITIONS. EXPERIMENTS HAVE BEEN CONDUCTED TO ELUCIDATE THE SCOPE OF THIS ETHER
  194503. ETHER, ETHER
  194504. ACETATE AND ACETATE
  194505. ETHER TRANSFORMATIONS.
  194506. 15116N
  194507. 2/28/96
  194508. AVCATALYTIC and EFFICIENT OF ALLYLIC and TERTIARY BENZYLIC ETHERS AND ESTERS WITH CE(IV)
  194509. 1994X    7299
  194510. 7306Y
  194511. 14108
  194512. CALO, V.
  194513. TetrahedronC
  194514. ORGANOCOPPER REAGENTS ALLYLIC DERIVATIVES GRIGNARD
  194515. REAGENTS ANCHIMERIC COORDINATION LEAVING GROUPS ALKYLATION REGIOCONTROL CARBOXYLATES STEREOCHEMISTRY REGIOCHEMISTRY 
  194516. uOPTICALLY ACTIVE ALLYLIC SULPHIDES 10
  194517. 13. BEARING TWO DIFFERENT LEAVING GROUPS, REACT WITH ORGANOCOPPER REAGENTS BY SELECTIVE SUBSTITUTION OF THE HETEROCYCLE MOIETY LEADING TO OPTICALLY ACTIVE HOMOALLYLIC PIVALATES WITH CHEMO
  194518. , REGIO
  194519.  AND ENANTIO
  194520. CONTROL. THIS SELECTIVITY SEEMS TO BE RELATED TO THE COORDINATION EXERTED BY THE HETEROCYCLIC NUCLEUS TOWARDS THE ORGANOMETAL.
  194521. 15117N
  194522. 2/28/96
  194523. A[CHELATION
  194524. CONTROLLED CHEMO
  194525. , REGIO
  194526.  and ENANTIO
  194527. SELECTIVE SYNTHESIS OF HOMOALLYLIC ALCOHOLS
  194528. 1994X    7283
  194529. 7292Y
  194530. 14109
  194531. PEREZPEREZ, M. J.
  194532. TetrahedronCUUNSATURATED CARBENES MILD GENERATION WITTIG REACTION VINYL PYRIMIDINE KETONES ETHERS 
  194533. REACTION OF O
  194534. MESYLCYANOHYDRINS OF FURANOS
  194535. ULOSE WITH SODIUM AZIDE AFFORDED ISOMERIC VINYLAZIDO COMPOUNDS. A MECHANISM INVOLVING AN ALKYLIDENE CARBENE IS PROPOSED AND THE INTERMEDIACY OF SUCH A CARBENE IS CONFIRMED BY STANDARD TRAPPING REACTIONS SUCH AS, ADDITION TO THE DOUBLE BOND OF CYCLOHEXENE OR INSERTION INTO THE SI
  194536. H OR O
  194537. H BONDS OF TRIETHYLSILANE OR METHANOL, RESPECTIVELY. THE ABOVE MENTIONED REACTION HAS BEEN CARRIED OUT IN DIFFERENT SOLVENTS (DICHLOROMETHANE, THF, NITROMETHANE, B9ACETONITRILE) TO YIELD A VARIETY OF HIGHLY FUNCTIONALIZED
  194538. 15118N
  194539. 2/28/96
  194540. AtALKYLIDENE CARBENES AS INTERMEDIATES IN THE SYNTHESIS OF HIGHLY FUNCTIONALIZED BRANCHED
  194541. CHAIN SUGARS and NUCLEOSIDES
  194542. 1994 X    7269
  194543. 7282Y
  194544. 14110
  194545. VITEVA, L. Z.
  194546. TetrahedronC
  194547. ASYMMETRIC ALDOL REACTIONS CONJUGATE ADDITION CARBONYL
  194548. COMPOUNDS ALPHA
  194549. ENONES REGIOSELECTIVITY STEREOCHEMISTRY KETONES STEREOSELECTIVITY DERIVATIVES MECHANISM 
  194550. THE SYNTHETIC POTENTIAL, REGIO
  194551.  AND STEREOSELECTIVITY OF TITANIUM DIALKYLAMIDE AND DIALKYLTHIOAMIDE ENOLATES AND ''ATE'' COMPLEXES IN REACTION WITH SOME CONJUGATE CARBONYL COMPOUNDS ARE INVESTIGATED. TITANIUM ENOLATES REACT PREFERENTIALLY IN 1,2
  194552. POSITION WHILE ''ATE'' COMPLEXES AFFORD 1,4
  194553. REGIOCONTROL. THE STEREOCHEMICAL BEHAVIOUR OF THE LATTER FOLLOWS IN GENERAL THE LITHIUM AND POTASSIUM PRECURSORS. MARKED INFLUENCE OF SOLVENT AND OF ELECTROPHILE GEOMETRY ON 1,4
  194554. STEREOSELECTIVITY WAS FOUNB3D WITH THE AMIDES BUT NOT WITH THE THIOANALOGS. THE
  194555. 15119N
  194556. 2/28/96
  194557. AjTITANIUM ENOLATES and ''ATE'' COMPLEXES OF N,N
  194558. DISUBSTITUTED AMIDES and THIOAMIDES IN THE MICHAEL REACTION
  194559. 1994X    7193
  194560. 7202Y
  194561. 14111
  194562. A    KRIEF, A.
  194563. TetrahedronC<CYCLIZATIONS ROUTE TETRAHYDROFURANS SELENOACETALS ALDEHYDES K
  194564. ARYLCYCLOALKANES ARE PRODUCED FROM OMEGA
  194565. ALKENYL BENZYLSELENIDES ON REACTION WITH ALKYLLITHIUMS OR ON LEWIS ACID MEDIATED ELECTROPHILIC CYCLISATION.M
  194566. 15120N
  194567. 2/28/96
  194568. A<SYNTHESIS OF ARYLCYCLOALKANES FROM w
  194569. ALKENYL BENZYLSELENIDES
  194570. 1994X    7177
  194571. 7192Y
  194572. 14112
  194573. BOONS, G. J.
  194574. Tetrahedron
  194575. uALPHA
  194576. HYDROXY ACIDS HAVE BEEN REACTED WITH BIS
  194577. DIHYDROPYRANS TO GIVE DISPIROKETAL ADDUCTS (1,8,13,16
  194578. TETRAOXADISPIRO[5.0.5.4]
  194579. HEXADECAN
  194580. ONES). THE ENOLATES DERIVED FROM THESE COMPOUND UNDERGO REACTION WITH ELECTROPHILES WITH GENERALLY HIGH LEVELS OF DIASTEREOSELECTIVITY. SUBSEQUENT DEPROTECTION OF THESE COMPOUNDS GIVES ALPHA
  194581. HYDROXY ESTERS OF HIGH ENANTIOMERIC EXCESS.
  194582. 15121N
  194583. 2/28/96
  194584. AeDISPIROKETALS IN SYNTHESIS .10. FURTHER REACTIONS OF DISPOKE PROTECTED LACTATE and GLYCOLATE ENOLATES
  194585. 1994 X    7157
  194586. 7176Y
  194587. 14113
  194588. MARKO, I. E.
  194589. TetrahedronCCSTEREOSELECTIVE FORMATION CYCLIC ETHERS TETRAHYDROPYRANS EFFICIENT K}THE ISMS REACTION HAS BEEN USED TO EFFICIENTLY CONSTRUCT THE RIGHT
  194590. HAND PORTION 3 OF THE ANTIFUNGAL ANTIBIOTIC AMBRUTICINE 1.M
  194591. 15122N
  194592. 2/28/96
  194593. A`THE INTRAMOLECULAR SILYL
  194594. MODIFIED SAKURAI (ISMS) REACTION. SYNTHETIC STUDIES TOWARDS AMBRUTICINE
  194595. 1994 X    7141
  194596. 7156Y
  194597. 14114
  194598. LOLKEMA, L. D. M.
  194599. TetrahedronCLGLYOXYLATE ENE REACTION SILICON ESTERS TETRAHYDROPYRIDINES TETRAHYDROFURANS 
  194600. THE 2
  194601. OXONIA COPE REARRANGEMENT IS SHOWN TO PLAY AN IMPORTANT ROLE IN LEWIS ACID
  194602. INDUCED R
  194603. CYCLIZATION REACTIONS OF A VARIETY OF METHYL 2
  194604. ACETOXY
  194605. ALKEN
  194606. OXY) ACETATES TO 5
  194607.  AND 6
  194608. MEMBERED RING ETHERS. THE INFLUENCE OF THIS [3,3]
  194609. SIGMATROPIC REARRANGEMENT ON THE REGIO
  194610.  AND STEREOCHEMICAL OUTCOME OF THE CYCLIZATION IS EVALUATED BY STUDYING THREE TYPES OF SUBSTRATES, NAMELY (1) FOUR CHAIN
  194611. SUBSTITUTED PRECURSORS, (2) THREE SILICON
  194612. SUBSTITUTED PRECURSORS (ALLYL
  194613.  AND VINYLSILANES) AND (3) B7TWO ENANTIOPURE PRECURSORS. CONTROLLING FACTORS ARE THE
  194614. 15123N
  194615. 2/28/96
  194616. AoSTUDIES ON THE ROLE OF THE 2
  194617. OXONIA COPE REARRANGEMENT IN p
  194618. CYCLIZATIONS OF A
  194619. METHOXYCARBONYL OXYCARBENIUM IONS
  194620. 1994X    7129
  194621. 7140Y
  194622. 14115
  194623. LOLKEMA, L. D. M.
  194624. TetrahedronC
  194625. GLYCINE CATION EQUIVALENTS PIPECOLIC ACID
  194626. DERIVATIVES ACETAL
  194627. INITIATED CYCLIZATIONS CYCLIC ETHERS CARBONYL
  194628. COMPOUNDS PROMOTED CYCLIZATION SELECTIVE SYNTHESIS OLEFIN CYCLIZATION LEWIS
  194629. ACIDS AMINO
  194630. ACIDS 
  194631. MEDIATED CYCLIZATION REACTIONS ARE DESCRIBED OF SEVEN METHYL 2
  194632. ACETOXY
  194633. ALKEN
  194634. OXY)ACETATES WITH DIFFERENT CHAIN SUBSTITUTION. THE MAJOR PRODUCT OF THE TIN TETRACHLORIDE
  194635. INDUCED CYCLIZATION REACTION IS IN MOST CASES A TETRAHYDROPYRAN CONTAINING AN EQUATORIAL CARBOMETHOXY FUNCTION AT C2 AND AN AXIAL CHLORINE ATOM AT C4. THE MECHANISM OF ITS FORMATION INVOLVES A NET CIS
  194636. ADDITION OF THE INTERMEDIATE ALPHA
  194637. ESTER OXYCARBENIUM ION TO THE CARBON
  194638. CARBON DOUBLE BOND, MOST LIKELY CAUSED BB=Y A QUASI AXIAL ORIENTATION OF THE ESTER FUNCTION IN A CHAIR
  194639. 15124N
  194640. 2/28/96
  194641. CYCLIZATIONS OF A
  194642. METHOXYCARBONYL OXYCARBENIUM IONS:  SYNTHESIS OF OXACYCLIC CARBOXYLIC ESTERS
  194643. 1994X    7115
  194644. 7128Y
  194645. 14116
  194646. SASAKI, N. A.
  194647. TetrahedronC
  194648. ALPHA
  194649. AMINO
  194650. ACIDS ANT VENOM ALKALOIDS ASYMMETRIC
  194651. SYNTHESIS TRANS
  194652. DISUBSTITUTED PYRROLIDINES CHIRAL AUXILIARIES ENANTIOSELECTIVE SYNTHESIS CONVENIENT SYNTHESIS RADICAL ADDITIONS ALKYLATION TRANS
  194653. DIMETHYLPYRROLIDINE 
  194654. POT RING FORMATION USING (R)
  194655. 1 OR (S)
  194656. 1 AS A NUCLEOPHILE AND HOMACHIRAL GLYCIDYL TRIFLATE (R)
  194657. 2 OR (S)
  194658. 2 AS AN ELECTROPHILE PROVIDES A PIVOTAL INTERMEDIATE 4 WHICH CAN BE TRANSFORMED INTO A 2,5
  194659. DISUBSTITUTED PYRROLIDINE WITH ANY DESIRED STEREOCHEMISTRY AT THE C
  194660. 2 AND C
  194661. 5 POSITIONS
  194662. 15125N
  194663. 2/28/96
  194664. ALA NOVEL METHOD FOR CHIROSPECIFIC SYNTHESIS OF 2,5
  194665. DISUBSTITUTED PYRROLIDINES
  194666. 1994 X    7093
  194667. 7108Y
  194668. 14117
  194669. DEBOECK, B.
  194670. TetrahedronC
  194671. HYDROGEN TRANSFER 
  194672. ,THE TITLE ONE
  194673. POT REACTION OCCURS THROUGH A SEQUENCE OF [2+2] CYCLOADDITION RING OPENING TO DIENAMINES AND FORMATION OF A 1,5
  194674. DIPOLE BY [1,6] HYDROGEN
  194675. SHIFT. THIS INTERMEDIATE MAY CYCLIZE OR IN STERICALLY SUITABLE CASES AND AT LOWER TEMPERATURES, LEAD TO ISOLABLE N
  194676. VINYL ENAMINES BY PROTON TRANSFER.
  194677. 15126N
  194678. 2/28/96
  194679. CYCLIZATION OF TERTIARY AMINES .3. CAPTODATIVE OR PUSH
  194680. PULL ENAMINES FORM PYRROLINES, PYRROLIZIDINES and THEIR RING HOMOLOGUES WITH DIMETHYL ACETYLENEDICARBOXYLATE IN A HIGHLY DIASTEREOSELECTIVE REACTION
  194681. 1994 X    7075
  194682. 7092Y
  194683. 14118
  194684. DAMM, W.
  194685. TetrahedronC
  194686. ASYMMETRIC INDUCTION REDUCTIVE ALKYLATION ACYCLIC RADICALS BROMO ESTERS AMINO
  194687. ACIDS MODEL 1,2
  194688. STEREOINDUCTION DERIVATIVES ENAMINES 
  194689. THE BARTON ESTERS 17 AND 18, SYNTHESIZED FROM THE CORRESPONDING AMINO ACID DERIVATIVES 6 AND 14, WERE IRRADIATED IN SITU WITH OR WITHOUT AN EXTERNAL TRAP. THUS, THIOPYRIDINES 22 AND 23, PHENYLSELENIDES 24 AND 25, ESTERS 26 AND 27 AS WELL AS DEUTERATED PRODUCTS 34 AND 35 WERE ISOLATED WHEN THE RADICAL 20 AND 21 WERE TRAPPED WITH BARTON ESTERS 17 AND 18 OR WITH PHSESEPH, METHYL ACRYLATE OR BU(3)SND. IN ALL CASES THE ANTI ISOMERS WERE ISOLATED AS THE MAJOR PRODUCTS IN MODERATE TO EXCELLENT SEB3LECTIVITY. THE STEREOCHEMICAL COURSE OF THE RADICAL
  194690. 15127N
  194691. 2/28/96
  194692. A9STEREOSELECTIVE REACTIONS OF A
  194693. IMIDE SUBSTITUTED RADICALS
  194694. 1994 X    7029
  194695. 7048Y
  194696. 14119
  194697. A    LABBE, G.
  194698. TetrahedronCPCYCLOADDITION
  194699. ELIMINATION
  194700. REACTIONS PI
  194701. BONDED SIV PARTICIPATION NITRILES SWITCH 
  194702. FUSED 1,2,4
  194703. THIADIAZOLES (14
  194704. 18 AND 26
  194705. 31) ARE CONVENIENTLY PREPARED BY REACTING THE CHLOROTHIADIAZOLONE 12 WITH OMEGA
  194706. AMINONITRILES AND AMINOAZOLES. DURING THESE REACTIONS THE ORIGINAL THIADIAZOLE RING IS OPENED AND A NEW, FUSED THIADIAZOLE RIG IS FORMED, PROBABLY VIA A HYPERVALENT SULFUR INTERMEDIATE. THE PRODUCTS DERIVED FROM THE AMINOAZOLES WERE ANALYZED BY X
  194707. RAY CRYSTALLOGRAPHY AND FOUND TO HAVE STRUCTURES DIFFERENT FROM THOSE PUBLISHED EARLIER.(7)
  194708. 15128N
  194709. 2/28/96
  194710. AOSYNTHESIS OF FUSED 1,2,4
  194711. THIADIAZOLES FROM 5
  194712. CHLORO
  194713. 1,2,4
  194714. THIADIAZOL
  194715. 3(2H)
  194716. 1994 X    7019
  194717. 7028Y
  194718. 14120
  194719. SEGUNDO, A.
  194720. OrganometallicsC
  194721. CARBENE COMPLEXES ALKINYLCARBENE COMPLEXES REACTIVITY AUXILIARIES THERMAL REARRANGEMENT PENTACARBONYL GROUPS STEREOCHEMISTRY LIGANDS M
  194722. 15129N
  194723. 2/28/96
  194724. A^REACTIONS OF ALKYNOLS WITH (ALKYNYLALKOXYCARBENE) METAL COMPLEXES (METAL = CHROMIUM, TUNGSTEN)
  194725. 1994 X    2467
  194726. 2471Y
  194727. 14121
  194728. Hwu, J. R.B
  194729. OrganometallicsM
  194730. 15130N
  194731. 2/28/96
  194732. INTERCONVERSIONS AMONG A
  194733. (TRIMETHYLSILYL) ALKOXIDES, A
  194734. TRIMETHYLSILOXY CARBANIONS, and CARBONYL COMPOUNDS ACCOMPANIED BY THE TRIMETHYLSILYL ANION
  194735. 1994X    2461
  194736. 2466Y
  194737. 14122
  194738. INDOLESE, A. F.
  194739. OrganometallicsC
  194740. REDUCTIVE ELIMINATION METAL
  194741. COMPLEXES SYNDIOTACTIC POLY<(S)
  194742. METHYL
  194743. HEXENE> BIPHENYL SERIES ALCOHOLS POLYMERIZATION CONFIGURATION POLYMERS OLEFINS M
  194744. 15131N
  194745. 2/28/96
  194746. ENANTIOSELECTIVE NICKEL CATALYZED GRIGNARD CROSS COUPLING OF ALLYL ELECTROPHILES 
  194747.  THE INFLUENCE OF THE ALKYL GROUP OF THE GRIGNARD REAGENT
  194748. 1994X    2230
  194749. 2234Y
  194750. 14123
  194751. HUGHES, R. P.
  194752. J. Organomet. Chem.
  194753. CiRHODIUM CYCLOBUTADIENE CARBON CARBON BONDS VINYLCYCLOPROPENE MECHANISM REARRANGEMENT MOLECULAR
  194754. STRUCTURE M
  194755. 15132N
  194756. 2/28/96
  194757. UNUSUAL RHODIUM PROMOTED REACTION OF A VINYLCYCLOPROPENE to GIVE A CYCLOBUTADIENE LIGAND 
  194758.  FORMATION OF (h5
  194759. PENTAMETHYLCYCLOPENTADIENYL)
  194760. BUTYL(METHYL )CYCLOBUTADIENE]RHODIUM
  194761. 1994 X
  194762. 14124
  194763. A    KUMAR, V.
  194764. J. Organomet. Chem.CVIRON PHOSPHORUS CARBONYL CARBENE CLUSTER CRYSTAL STRUCTURE METAL
  194765. CARBONYLS PHOSPHORUS M
  194766. 15133N
  194767. 2/28/96
  194768. A3INSERTION OF A CARBENOID UNIT INTO AN FE2P2 CLUSTER
  194769. 1994 X
  194770. 14125
  194771. A    KLAUI, W.
  194772. J. Organomet. Chem.CrPALLADIUM COBALT ALKYL CRYSTAL STRUCTURE OXYGEN LIGAND TRIPODAL LIGAND ORGANOMETALLIC CHEMISTRY CRYSTAL
  194773. STRUCTURE M
  194774. 15134N
  194775. 2/28/96
  194776. AmORGANOPALLADIUM COMPLEXES WITH PALLADIUM AT THE OXIDATION STAGE
  194777. +IV ARE STABILIZED BY TRIPODAL OXYGEN LIGANDS
  194778. 1994 X
  194779. 14126
  194780. SHAFIQ, F.
  194781. J. Organomet. Chem.C
  194782. RHODIUM A
  194783. FRAME COMPLEXES PROTONATION BINUCLEAR A
  194784. FRAME COMPLEXES MU
  194785. IMIDO COMPLEXES HYDROGENATION REACTIONS INDUCED POLARIZATION METAL LIGAND M
  194786. 15135N
  194787. 2/28/96
  194788. AVSYNTHESIS, STRUCTURE and REACTIVITY OF BINUCLEAR RHODIUM DICATIONIC CARBONYL COMPLEXES
  194789. 1994X
  194790. 14127
  194791. YOKOMATSU, T.
  194792. 15136N
  194793. 2/28/96
  194794. GROUP IV
  194795. METaL
  194796. CATALYZED AMINOLYSIS OF N
  194797. OXAZOLIDINONES:  APPLICATIONS to THE CHEMOSELECTIVE and ENANTIOSELECTIVE CARBONYLATION OF PRIMARY ALKYLAMINES
  194798. 1994 X    3506
  194799. 3508Y
  194800. 14128
  194801. YAMASHITA, M.
  194802. 15137N
  194803. 2/28/96
  194804. AQTHE REACTION OF SODIUM HYDROGEN TELLURIDE WITH A,b
  194805. UNSATURATED CARBONYL COMPOUNDS
  194806. 1994 X    3500
  194807. 3502Y
  194808. 14129
  194809. HOLLIS, W. G.
  194810. 15138N
  194811. 2/28/96
  194812. AWREACTION OF TRIALKYLBORANES WITH NITRONES:  A NOVEL ROUTE to A
  194813. ALKYLATED HYDROXYLAMINES
  194814. 1994 X    3485
  194815. 3486Y
  194816. 14130
  194817. ARNONE, A.
  194818. FLUORO
  194819. ORGANIC COMPOUNDS ASYMMETRIC
  194820. SYNTHESIS DIFLUOROALKYL RADICALS SULFUR SUBSTITUENTS CARRYING FLUORINE CHAIN REACTIONS OPTICALLY PURE ESTERS SULFOXIDES ABSOLUTE M
  194821. 15139N
  194822. 2/28/96
  194823. SYNTHESIS OF ENANTIOMERICALLY PURE GEM
  194824. DIFLUOROCYCLOHEXANE DERIVATIVES BY INTRAMOLECULAR TRAPPING OF A,A
  194825. DIFLUOROALKYL RADICALS
  194826. 1994 X    3459
  194827. 3466Y
  194828. 14131
  194829. BOGER, D. L.
  194830. CYCLO
  194831. ADDITION REACTIONS DELOCALIZED SINGLET VINYLCARBENES 3
  194832. CARBON 1,1
  194833. DIPOLES 1,3
  194834. DIPOLES + 2
  194835. CARBON CYCLOADDITION ECHINORUBER SP
  194836. NOV SYNTHETIC APPLICATIONS THERMAL
  194837. REACTIONS DOUBLE
  194838. BONDS RED PIGMENT PARTICIPATION M
  194839. 15140N
  194840. 2/28/96
  194841. A{DIELS
  194842. ALDER REACTIONS OF CYCLOPROPENONE KETALS:  A CONCISE TROPOLONE ANNULATION APPLICABLE to RUBROLONE C RING INTRODUCTION
  194843. 1994 X    3453
  194844. 3458Y
  194845. 14132
  194846. MOLANDER, G. A.
  194847. REMOTE ASYMMETRIC INDUCTION WITTIG RING CONTRACTION ALPHA
  194848. AMINO
  194849. ACIDS ORGANIC
  194850. SYNTHESIS SIDE
  194851. CHAIN ENANTIOSELECTIVE SYNTHESIS STEREOSELECTIVE SYNTHESIS ADDITION
  194852. REACTIONS VITAMIN
  194853. E SIGMATROPIC REARRANGEMENTS 
  194854. INTRAMOLECULAR NUCLEOPHILIC 4
  194855. HYDROXY KETONES SAMARIUM IODIDE IODO CYCLIZATION
  194856. 15141N
  194857. 2/28/96
  194858. INTRAMOLECULAR NUCLEOPHILIC ACYL SUBSTITUTION REACTIONS MEDIATED BY SAMARIUM(II) IODIDE:  A CONVERGENT APPROACH to THE PREPARATION OF ENANTIOMERICALLY ENRICHED 4
  194859. HYDROXY KETONES FROM 3
  194860. IODOPROPYL CARBOXYLATES
  194861. 1994 X    3445
  194862. 3452Y
  194863. 14133
  194864. TABER, D. F.
  194865. JOCCaHAPLOPHYLLUM
  194866. TUBERCULATUM ASYMMETRIC EPOXIDATION POLYETHER ACETOGENINS BISEPOXIDE STRATEGY MODEL M
  194867. 15142N
  194868. 2/28/96
  194869. A/CASCADE CYCLIZATION:  SYNTHESIS OF (+)
  194870. TUBERINE
  194871. 1994X    3442
  194872. 3444Y
  194873. 14134
  194874. ARCE, E.
  194875. RUANO 
  194876. REMOTE STEREOGENIC CENTER ENANTIOSELECTIVE SYNTHESIS CONFORMATIONAL MODEL 4+2 CYCLOADDITION CHIRAL DIENES SULFOXIDES BEARING 4
  194877. NITROCYCLOHEXANONES STEREOCHEMISTRY SUBSTITUENTS 
  194878. DIELS
  194879. ALDER ASYMMETRIC REVIEW SULFOXIDE LEWIS ACID 2,3
  194880. SIGMATROPICM
  194881. 15143N
  194882. 2/28/96
  194883. FIRST DIELS
  194884. ALDER REACTIONS OF ENANTIOMERICALLY PURE 1
  194885. TOLYLSULFINYL DIENES:  STRAIGHTFORWARD ACCESS to CYCLOHEXENOLS THROUGH TANDEM CYCLOADDITION/[2,3]
  194886. SIGMATROPIC REARRANGEMENT
  194887. 1994 X    3421
  194888. 3426Y
  194889. 14135
  194890. CABLEWSKI, T.
  194891. OVENS M
  194892. 15144N
  194893. 2/28/96
  194894. ASDEVELOPMENT and APPLICATION OF A CONTINUOUS MICROWAVE REACTOR FOR ORGANIC SYNTHESIS
  194895. 1994 X    3408
  194896. 3412Y
  194897. 14136
  194898. MCKEW, J. C. 
  194899. JOCC?GAMMA
  194900. BUTYROLACTONES CLAISEN REARRANGEMENT LACTONIZATION ROUTE M
  194901. 15145N
  194902. 2/28/96
  194903. A{DOUBLY DIASTEREOSELECTIVE IODOLACTONIZATIONS:  OLEFIN and FACE SELECTIVITY IN NONA
  194904. DIENE
  194905. CARBOXYLIC ACID CYCLIZATIONS
  194906. 1994X    3389
  194907. 3393Y
  194908. 14137
  194909. AKAZOME, M.
  194910. WATANABE
  194911.  AROMATIC NITRO
  194912. COMPOUNDS CARBON
  194913. MONOXIDE PALLADIUM(II)
  194914. CATALYZED COPOLYMERIZATION ALIPHATIC
  194915. ALDEHYDES CARBONYLATION OLEFINS REARRANGEMENTS TRANSFORMATION DINITROARENES DEOXYGENATION 
  194916. METAL TRANSITION NITRO AROMATIC PALLADIUM CYCLIZATION INDOLE COURSE HETEROCYCLE INDAZOLE METHOD SYNTHESIS
  194917. 15146N
  194918. 2/28/96
  194919. PALLADIUM COMPLEX
  194920. CATALYZED REDUCTIVE N
  194921. HETEROCYCLIZATION OF NITROARENES:  NOVEL SYNTHESIS OF INDOLE and 2H
  194922. INDAZOLE DERIVATIVES
  194923. 1994 X    3375
  194924. 3380Y
  194925. 14138
  194926. CAPELLA, L.
  194927. LACTAM ANTIBIOTICS ORGANIC
  194928. SYNTHESIS VINYL RADICALS PROMOTED CYCLIZATION DIPHENYL DISULFIDE ORGANOTIN REAGENTS CHAIN REACTIONS RING
  194929. EXPANSION ROUTE ARYL M
  194930. 15147N
  194931. 2/28/96
  194932. TIN RADICAL ADDITION to ALKYNYL SULFIDES:  REACTIVITY OF THE INTERMEDIATE THIOALKYL
  194933. SUBSTITUTED b
  194934. (TRIBUTYLSTANNYL)VINYL RADICALS
  194935. 1994 X    3368
  194936. 3374Y
  194937. 14139
  194938. SUGA, H.
  194939. ASYMMETRIC ALDOL REACTION CHIRAL FERROCENYLPHOSPHINE
  194940. GOLD(I) COMPLEXES AMINO
  194941. ACIDS ALPHA
  194942. ISOCYANOCARBOXYLATES STEREOSELECTIVE SYNTHESIS LEWIS ACID ISOCYANOACETATE ALDEHYDES M
  194943. 15148N
  194944. 2/28/96
  194945. HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF 2
  194946. OXAZOLINE
  194947. CARBOXYLATES BY FORMAL [3+2] CYCLOADDITIONS OF A 5
  194948. ALKOXYOXAZOLE WITH A
  194949. ALKOXY ALDEHYDES CATALYZED BY TIN(IV) CHLORIDE
  194950. 1994 X    3359
  194951. 3364Y
  194952. 14140
  194953. ADAM, W.
  194954. TRANSPOSED ALLYLIC ALCOHOLS TRIMETHYLSILYL GROUP ORGANIC
  194955. SYNTHESIS SINGLET OXYGEN VINYL SILANES ALLENE OXIDES ENE REACTION KETONES PHOTOOXYGENATION ALDEHYDES M
  194956. 15149N
  194957. 2/28/96
  194958. A}HIGHLY REGIO
  194959.  and DIASTEREOSELECTIVE ONE
  194960. POT SYNTHESIS OF SILYL EPOXY ALCOHOLS and VINYLSILANES BY DIRECT HYDROXY
  194961. EPOXIDATION
  194962. 1994 X    3341
  194963. 3346Y
  194964. 14141
  194965. ADAM, W.
  194966. TRANSPOSED ALLYLIC ALCOHOLS SUBSTITUTED TETRAMETHYLETHYLENES STEREOSELECTIVE SYNTHESIS ROTATIONAL BARRIERS KETONES PHOTOOXYGENATION ALPHA TRIAZOLINEDIONE DERIVATIVES CONDENSATION M
  194967. 15150N
  194968. 2/28/96
  194969. AXREGIOSELECTIVITY OF THE SINGLET OXYGEN ENE REACTION (SCHENCK REACTION) WITH VINYLSILANES
  194970. 1994 X    3335
  194971. 3340Y
  194972. 14142
  194973. A    MIURA, Y.
  194974. CENTERED FREE
  194975. RADICALS PENDANT NITROXIDE RADICALS ELECTRON
  194976. RESONANCE METHYL SUBSTITUTION ESR POLY(1,3
  194977. PHENYLENEETHYNYLENE) POLY(ETHYNYLBENZENE) DERIVATIVES ENDOR M
  194978. 15151N
  194979. 2/28/96
  194980. GENERATION, ISOLATION, and CHARACTERIZATION OF N
  194981. (ARYLTHIO)
  194982. BUTYL
  194983.  and N
  194984. (ARYLTHIO)
  194985. BUTYL
  194986. PYRENYLAMINYL RADICALS
  194987. 1994 X    3294
  194988. 3300Y
  194989. 14143
  194990. MILLER, R. S.
  194991. PENICILLIN KETONES M
  194992. 15152N
  194993. 2/28/96
  194994. ASSTEREOCHEMISTRY OF BASE
  194995. CATALYZED ADDITION OF THIOPHENOL to 3
  194996. H CARBACEPHALOSPORINS
  194997. 1994X    3289
  194998. 3293Y
  194999. 14144
  195000. Liu, H.B
  195001. JOCC?REGIOSPECIFIC SYNTHESIS SUBSTITUTED QUINONES CYCLOBUTENEDIONES M
  195002. 15153N
  195003. 2/28/96
  195004. SYNTHETIC UTILITY OF ALKENYLCYCLOBUTENEDIONE MONOKETALS. MICHAEL ADDITIONS and THE SYNTHESIS OF A NATURAL BENZOFURANOSESQUITERPENEQUINONE
  195005. 1994 X    3284
  195006. 3288Y
  195007. 14145
  195008. MUKHERJEE, A.
  195009. JOCC+ELECTRONIC CONTROL HYPERCONJUGATION CARBON M
  195010. 15154N
  195011. 2/28/96
  195012. A(FACE SELECTION IN CLAISEN REARRANGEMENTS
  195013. 1994 X    3270
  195014. 3274Y
  195015. 14146
  195016. BODEPUDI, V. R.
  195017. JOCCVNUCLEOPHILIC
  195018. ADDITION ELECTRONIC CONTROL STEREOCHEMISTRY PROTONATION KETONES STEP NMR M
  195019. 15155N
  195020. 2/28/96
  195021. A/FACE SELECTION IN THE CAPTURE OF ANIONIC CARBON
  195022. 1994 X    3265
  195023. 3269Y
  195024. 14147
  195025. CURRAN, D. P.
  195026. JOCCFMOLECULAR RECOGNITION COMPUTER
  195027. SIMULATIONS STEREOSELECTIVITY SOLVENTS M
  195028. 15156N
  195029. 2/28/96
  195030. AcALTERING THE STEREOCHEMISTRY OF ALLYLATION REACTIONS OF CYCLIC A
  195031. SULFINYL RADICALS WITH DIARYLUREAS
  195032. 1994 X    3259
  195033. 3261Y
  195034. 14148
  195035. A    PADWA, A.
  195036. ORGANIC
  195037. SYNTHESIS 3+2 CYCLIZATION ELECTROPHILIC SUBSTITUTION CYCLOPENTENYL SULFONES ANNULATION APPROACH REAGENTS CYCLOADDITION CONSTRUCTION ELIMINATION STRATEGY M
  195038. 15157N
  195039. 2/28/96
  195040. A NEW CYCLOPENTANNULATION APPROACH to BICYCLO[3.3.0]OCTENES EMPLOYING A TANDEM MICHAEL ADDITION
  195041. [3+2]
  195042. ANIONIC CYCLIZATION SEQUENCE
  195043. 1994 X    3256
  195044. 3258Y
  195045. 14149
  195046. JUNG, M. E.
  195047. OF4949
  195048. III K
  195049. 15158N
  195050. 2/28/96
  195051. VICARIOUS NUCLEOPHILIC AROMATIC SUBSTITUTION VIA TRAPPING OF AN A
  195052. KETOSULFONIUM ION GENERATED BY PUMMERER
  195053. TYPE REARRANGEMENT OF 2
  195054. (PHENYLSULFINYL)PHENOLS:  PREPARATION OF BIARYLS
  195055. 1994 X    3248
  195056. 3249Y
  195057. 14150
  195058. SCHLESSINGER, R. H.
  195059. ENANTIOSELECTIVE SYNTHESIS 4
  195060. NITROCYCLOHEXANONES 
  195061. FURAN DIELS
  195062. ALDER AMINO WRITING STUDENT TARGET DIASTEREOSELECTIVE NATURAL PRODUCT RING OPENINGM
  195063. 15159N
  195064. 2/28/96
  195065. AXDIASTEREOSELECTIVE DIELS
  195066. ALDER REACTIONS USING FURAN SUBSTITUTED WITH A NONRACEMIC AMINE
  195067. 1994X    3246
  195068. 3247Y
  195069. 14151
  195070. DAVIS, F. A.
  195071. OPENING REACTION ALPHA
  195072. AMINO
  195073. ACIDS 2
  195074. AZIRIDINECARBOXYLIC ACID CONVENIENT SYNTHESIS ESTERS DERIVATIVES AZIRIDINES STEREOISOMERS SULFINIMINES REMOVAL M
  195075. 15160N
  195076. 2/28/96
  195077. A[ASYMMETRIC SYNTHESIS and REACTIONS OF CIS
  195078. TOLUENESULFINYL)AZIRIDINE
  195079. CARBOXYLIC ACIDS
  195080. 1994 X    3243
  195081. 3245Y
  195082. 14152
  195083. LOVE, B. E.
  195084. 15161N
  195085. 2/28/96
  195086. A"PREPARATION OF 1
  195087. CARBOLINES
  195088. 1994 X    3219
  195089. 3222Y
  195090. 14153
  195091. GIBSON, F. S.
  195092. 15162N
  195093. 2/28/96
  195094. AtSELECTIVE REMOVAL OF AN N
  195095. BOC PROTECTING GROUP IN THE PRESENCE OF A TERT
  195096. BUTYL ESTER and OTHER ACID
  195097. SENSITIVE GROUPS
  195098. 1994 X    3216
  195099. 3218Y
  195100. 14154
  195101. ALMENA, J.
  195102. ORGANO
  195103. LITHIUM COMPOUNDS BARBIER
  195104. TYPE CARBONYL
  195105. COMPOUNDS 4,4'
  195106. BUTYLBIPHENYL
  195107. CATALYZED LITHIATION REACTIVITY REAGENTS KETONES N
  195108. LITHIO
  195109. LITHIOETHYL)BENZAMIDE 3
  195110. CHLORO
  195111. CHLOROMETHYLPROPENE DERIVATIVES M
  195112. 15163N
  195113. 2/28/96
  195114. AjN,2
  195115. DILITHIOALKYLAMINES FROM AZIRIDINES BY NAPHTHALENE
  195116. CATALYZED REDUCTIVE OPENING. SYNTHETIC APPLICATIONS
  195117. 1994 X    3210
  195118. 3215Y
  195119. 14155
  195120. BONETE, P.
  195121. METHYL 3
  195122. PHENYLSULFONYL ORTHOPROPIONATE HOMOENOLATE ANION ORGANIC
  195123. SYNTHESIS GAMMA
  195124. LACTONES CONVENIENT SYNTHESIS CARBONYL
  195125. COMPOUNDS DELTA
  195126. LACTONES DERIVATIVES BUTENOLIDES REACTIVITY M
  195127. 15164N
  195128. 2/28/96
  195129. ArLITHIUM 3
  195130. LITHIO
  195131. TOSYLALKANOATES:  b
  195132. ACYLVINYL ANION EQUIVALENTS OF b
  195133. LITHIATED A,b
  195134. UNSATURATED CARBOXYLIC ACIDS
  195135. 1994 X    3202
  195136. 3209Y
  195137. 14156
  195138. MARINO, J. P.
  195139. ASYMMETRIC
  195140. SYNTHESIS VINYL SULFOXIDES ENANTIOSELECTIVE SYNTHESIS CONJUGATE ADDITION PARA
  195141. TOLYL SUBSTITUTION INDUCTION REAGENTS M
  195142. 15165N
  195143. 2/28/96
  195144. SYNTHESIS OF ENANTIOPURE 2
  195145. MALONYLVINYL SULFOXIDES VIA ADDITION
  195146. ELIMINATION REACTIONS OF 2
  195147.  and 2
  195148. (MESYLOXY)VINYL SULFOXIDES
  195149. 1994X    3193
  195150. 3201Y
  195151. 14157
  195152. MOLANDER, G. A.
  195153. DISSOCIATION ENERGIES DIELS
  195154. ALDER REACTION 8
  195155. MEMBERED RINGS MACROCYCLIZATION MACROLIDES KETONES MOLECULES LACTONES CLOSURE SYSTEM 
  195156.  RADICAL SAMARIUM CYCLIZATION KETONE EIGHT MEMBERED MEDIUM RING ENDO OLEFINICM
  195157. 15166N
  195158. 2/28/96
  195159. AkSYNTHESIS OF SUBSTITUTED CYCLOOCTANOLS BY A SAMARIUM(II) IODIDE PROMOTED 8
  195160. ENDO RADICAL CYCLIZATION PROCESS
  195161. 1994X    3186
  195162. 3192Y
  195163. 14158
  195164. BAXTER, E. W.
  195165. POTENTIAL SIALIDASE INHIBITORS ALPHA
  195166. GLUCOSIDASE INHIBITORS ENZYMATIC ALDOL CONDENSATION BETA
  195167. GLUCOPYRANOSE PRACTICAL SYNTHESIS ASYMMETRIC
  195168. SYNTHESIS ORGANIC
  195169. SYNTHESIS CARBOHYDRATE
  195170. DERIVATIVES ISOMERIC COMPOSITION PHOTO
  195171. BROMINATION M
  195172. 15167N
  195173. 2/28/96
  195174. AYEXPEDITIOUS SYNTHESIS OF AZASUGARS BY THE DOUBLE REDUCTIVE AMINATION OF DICARBONYL SUGARS
  195175. 14159
  195176. SETO, M.
  195177. JOCC~HIGHLY EFFICIENT PRACTICAL APPROACH CRYSTAL
  195178. STRUCTURE CARBON FRAMEWORK SIDE
  195179. CHAIN PHASE
  195180. II TAXOL STEREOCHEMISTRY SYSTEM AGENT M
  195181. 15168N
  195182. 2/28/96
  195183. AN EFFICIENT APPROACH TOWARD TAXANE ANALOGS:  ATROP
  195184.  and DIASTEREOSELECTIVE EIGHT
  195185. MEMBERED B RING CYCLIZATIONS FOR SYNTHESIS OF AROMATIC C
  195186. RING TAXININE DERIVATIVES
  195187. 1994X    3165
  195188. 3174Y
  195189. 14160
  195190. SCHICK, H.
  195191. JOCC%HYDROXY ESTERS METAL NICKEL REAGENTS M
  195192. 15169N
  195193. 2/28/96
  195194. SYNTHESIS OF A,A,b,b
  195195. TETRASUBSTITUTED b
  195196. LACTONES FROM KETONES, ETHYL A
  195197. BROMOISOBUTYRATE AND INDIUM OR ZINC. FACTORS INFLUENCING THE b
  195198. LACTONE FORMATION IN THE ELECTROCHEMICAL and THE CLASSICAL PROCEDURE OF THE REFORMATSKY REACTION
  195199. 1994 X    3161
  195200. 3164Y
  195201. 14161
  195202. Ahn, Y.B
  195203. CHELATION CONTROL CONTROLLED NUCLEOPHILIC ADDITIONS OBTAINING UNUSUAL EQUATORIAL AROMATIC RADICAL
  195204. ANIONS HIGHLY EFFECTIVE SYSTEM REDUCTIVE LITHIATION STEREOSELECTIVE SYNTHESIS ASYMMETRIC INDUCTION CARBONYL
  195205. COMPOUNDS PREPARATIVE METHOD M
  195206. 15170N
  195207. 2/28/96
  195208. A GENERAL DIASTEREOSELECTIVE SYNTHESIS OF SPIROACETALS RELATED TO THOSE IN IONOPHORES VIA THE REACTION OF LACTONES WITH CERIUM(III) g
  195209. CERIOALKOXIDE. MAD REVERSES THE DIASTEREOSELECTIVITY OF THE ADDITION OF METHYLMETALLICS to A b
  195210. KETO ETHER
  195211. 1994 X    3142
  195212. 3150Y
  195213. 14162
  195214. PALOMO, C.
  195215. ENOLATE IMINE CONDENSATION ZINC
  195216. TRIMETHYLCHLOROSILANE ENANTIOSPECIFIC SYNTHESIS 1,3
  195217. ASYMMETRIC INDUCTION OZONIDE FRAGMENTATION CONVENIENT PROCEDURE ADDITION
  195218. REACTIONS PEPTIDE
  195219. SYNTHESIS GENERAL
  195220. SYNTHESIS CHELATION CONTROL M
  195221. 15171N
  195222. 2/28/96
  195223. AhNEW SYNTHESIS OF A
  195224. AMINO ACID N
  195225. CARBOXY ANHYDRIDES THROUGH BAEYER
  195226. VILLIGER OXIDATION OF A
  195227. KETO b
  195228. LACTAMS
  195229. 1994 X    3123
  195230. 3130Y
  195231. 14163
  195232. KECK, G. E.
  195233. JOCC~SPIROKETAL FRAGMENT O
  195234. GLYCOPEPTIDES CARBOMYCIN
  195235. B ALLYLSTANNANES ALDEHYDES ESTERS LEUCOMYCIN
  195236. A3 PROTECTION CHELATION OXIDATION M
  195237. 15172N
  195238. 2/28/96
  195239. A$TOTAL SYNTHESIS OF (+)
  195240. CARBONOLIDE B
  195241. 1994X    3113
  195242. 3122Y
  195243. 14164
  195244. CRUDDEN, C. M.
  195245. JOCCdALKANE DEHYDROGENATION COMPLEXES CARBONYLATION ALDEHYDES STEREOCHEMISTRY GENERATION ALKENES KETONES M
  195246. 15173N
  195247. 2/28/96
  195248. THE REGIOSELECTIVE HYDROFORMYLATION OF VINYLSILANES. A REMARKABLE DIFFERENCE IN THE SELECTIVITY and REACTIVITY OF COBALT, RHODIUM, AND IRIDIUM CATALYSTS
  195249. 1994 X    3091
  195250. 3097Y
  195251. 14165
  195252. CHAMBERLIN, S.
  195253. WULFF
  195254. ADDITION
  195255. REACTIONS ORGANIC
  195256. SYNTHESIS CHROMIUM CYCLOADDITION ALKYNES ANNULATION ACETYLENES ROUTE 
  195257.  FISCHER CARBENE COMPLEX REGIOCHEM BENZANNULATION PHENOL ALKYNE SILICON INTRODUCTIONM
  195258. 15174N
  195259. 2/28/96
  195260. ALSYNTHONS FOR THE PARENT VINYL CARBENE COMPLEX IN THE BENZANNULATION REACTION
  195261. 1994X    3047
  195262. 3054Y
  195263. 14166
  195264. TANAKA, H.
  195265. METAL KETENE COMPLEXES BETA,GAMMA
  195266. UNSATURATED ESTERS DECARBOXYLATION
  195267. CARBONYLATION ACTIVE INTERMEDIATE SELECTIVE SYNTHESIS ALLYLIC CARBONATES RING EXPANSION ACID CHEMISTRY ACETATES M
  195268. 15175N
  195269. 2/28/96
  195270. PALLADIUM
  195271. CATALYZED CARBONYLATIVE [2+2] CYCLOADDITION FOR THE STEREOSELECTIVE SYNTHESIS OF EITHER CIS
  195272.  OR TRANS
  195273. ALKENYL b
  195274. LACTAMS
  195275. 1994X    3040
  195276. 3046Y
  195277. 14167
  195278. DELLA, E. W.
  195279. 13 COUPLING
  195280. CONSTANTS CARBOXYLIC
  195281. ACIDS <1.1.1>PROPELLANE RADICALS 1,3
  195282. DIIODOBICYCLO<1.1.1>PENTANE HALIDES M
  195283. 15176N
  195284. 2/28/96
  195285. ALSYNTHESIS OF SOME BRIDGEHEAD BRIDGEHEAD
  195286. DISUBSTITUTED BICYCLO[1.1.1]PENTANES
  195287. 1994 X    2986
  195288. 2996Y
  195289. 14168
  195290. A    ROZEN, S.
  195291. CONVERSION M
  195292. 15177N
  195293. 2/28/96
  195294. A1A NOVEL CARBONYL to CF2 TRANSFORMATION USING BRF3
  195295. 1994X
  195296. 2918Y
  195297. 14169
  195298. ALDULAYYMI, J. R.
  195299. J.C.S. Perkin Trans. 1
  195300. CYCLO
  195301. ADDITION REACTIONS DELOCALIZED SINGLET VINYLCARBENES 3
  195302. CARBON 1,1
  195303. DIPOLES 1,3
  195304. DIPOLES OPTICALLY
  195305. ACTIVE CYCLOPROPENE THERMAL
  195306. REACTIONS ORGANIC
  195307. SYNTHESIS KETALS PERCHLOROVINYLCARBENE GENERATION ROUTE M
  195308. 15178N
  195309. 2/28/96
  195310. Af1,2
  195311. DIBROMOALK
  195312. ENYLIDENES BY RING
  195313. OPENING OF 1,2
  195314. DIBROMO
  195315. ALKYLCYCLOPROPENES AT AMBIENT TEMPERATURE
  195316. 1994 X    1633
  195317. 1641Z
  195318. 14170
  195319. SHING, T. K. M.
  195320. J.C.S. Perkin Trans. 1C
  195321. ESTER SIDE
  195322. CHAIN QUASSINOID SKELETON ENANTIOSELECTIVE SYNTHESIS SELECTIVE HYDROGENATION ABSOLUTE
  195323. CONFIGURATION SODIUM
  195324. BOROHYDRIDE ASSIGNMENT CONVENIENT SYSTEM RING M
  195325. 15179N
  195326. 2/28/96
  195327. A=SYNTHESIS OF OPTICALLY ACTIVE TETRACYCLIC QUASSINOID SKELETON
  195328. 1994X    1625
  195329. 1631Z
  195330. 14171
  195331. JONCZYK, A.
  195332. J.C.S. Perkin Trans. 1C&BASIC
  195333. MEDIUM ORGANIC
  195334. ANIONS CATALYSIS M
  195335. 15180N
  195336. 2/28/96
  195337. REACTION OF 1,1
  195338. DICHLORO
  195339. (CHLOROMETHYL)CYCLOPROPANE WITH SOME CARBANIONS:  A SIMPLE SYNTHESIS OF 1,2
  195340. DISUBSTITUTED METHYLENECYCLOPROPANES
  195341. 1994X    1605
  195342. 1609Z
  195343. 14172
  195344. VILLA, M. J.
  195345. J.C.S. Perkin Trans. 1
  195346. PHENYLTHIO
  195347. MIGRATION ASYMMETRIC
  195348. SYNTHESIS CHIRAL CENTERS DIASTEREOSELECTIVITY ALKYLATION ALPHA PROTONATION INDUCTION ALCOHOLS SULFIDES M
  195349. 15181N
  195350. 2/28/96
  195351. TANDEM CONJUGATE ADDITION OF SILYLCUPRATE and BENZENESULFENYL CHLORIDE to UNSATURATED EsTERS:  STEREOSELECTIVE PREpARATION OF ANTI
  195352. DIMETHYLPHENYLSILYL
  195353. PHENYLTHIO ALDEHYDES
  195354. 1994X    1569
  195355. 1572Z
  195356. 14173
  195357. HUDLICKY, T.
  195358. J.C.S. Perkin Trans. 1C
  195359. PSEUDOMONAS
  195360. PUTIDA ENANTIODIVERGENT SYNTHESIS ENANTIOSELECTIVE SYNTHESIS STEREOSPECIFIC SYNTHESIS ACTIVE
  195361. SITE CHLOROBENZENE BIOCATALYSIS DERIVATIVES EPOXIDES BIOTRANSFORMATION M
  195362. 15182N
  195363. 2/28/96
  195364. MICROBIAL OXIDATION OF AROMATICS IN ENANTIOCONTROLLED SYNTHESIS .1. EXPEDIENT AND GENERAL ASYMMETRIC SYNTHESIS OF INOSITOLS and CARBOHYDRATES VIA AN UNUSUAL OXIDATION OF A POLARIZED DIENE WITH POTASSIUM PERMANGANATE
  195365. 1994 X    1553
  195366. 1567Z
  195367. 14174
  195368. ARMITAGE, M. A.
  195369. J.C.S. Perkin Trans. 1CdALPHA,BETA
  195370. UNSATURATED CARBONYL COMPOUND 1
  195371. ACYLETHENYL ANION EQUIVALENT ALDOL REACTION 1,4
  195372. ADDITION M
  195373. 15183
  195374. 2/28/96
  195375. A6A GENERAL SYNTHESIS OF 2
  195376. SUBSTITUTED CYCLOHEX
  195377. ENONES
  195378. 1994X    1551
  195379. 1552Z
  195380. 14175
  195381. ALDULAYYNI, A. R.
  195382. J.C.S. Perkin Trans. 1C
  195383. AMBIENT
  195384. TEMPERATURE M
  195385. 15184N
  195386. 2/28/96
  195387. A0A FLEXIBLE ROUTE to 1
  195388. BROMO
  195389. ALKYLCYCLOPROPENES
  195390. 1994 X    1547
  195391. 1548Z
  195392. 14176
  195393. A    SIMON, C.
  195394. HeterocyclesC
  195395. ALKALOIDS NALTREXONE M
  195396. 15185N
  195397. 2/28/96
  195398. APPLICATION OF THE MITSUNOBU REACTION IN THE MORPHINE SERIES 
  195399.  PREPARATION OF 6-b
  195400. AMINO
  195401. HYDROXYMORPHINE and 14
  195402. HYDROXYCODEINE DERIVATIVES
  195403. 1994X    1347
  195404. 1354Y
  195405. 14177
  195406. BOHRISCH, J.
  195407. HeterocyclesC
  195408. LACTAM ACETALS M
  195409. 15186N
  195410. 2/28/96
  195411. AuRING
  195412. CHAIN TRANSFORMATIONS OF SEMICYCLIC 3
  195413. CHLOROPROPENIMINIUM SALTS to w
  195414. AMINOALKYL
  195415. OXAZOLES USING HYDROXYLAMINE
  195416. 1994 X    1333
  195417. 1338Y
  195418. 14178
  195419. FARINA, F.
  195420. HeterocyclesC
  195421. DIPOLAR CYCLO
  195422. ADDITIONS DIELS
  195423. ALDER REACTIONS DIASTEREOFACIAL SELECTIVITY ASYMMETRIC
  195424. SYNTHESIS PSEUDOESTERS ESTERS STEREOSELECTIVITY REGIOSELECTIVITY CHEMISTRY LACTONES 
  195425. 15187N
  195426. 2/28/96
  195427. ADCYCLOADDITION OF NITRILE OXIDES to 4
  195428. OXOBUT
  195429. ENOIC ACID DERIVATIVES
  195430. 1994X    1307
  195431. 1316Y
  195432. 14179
  195433. TOUSSAINT, D.
  195434. HeterocyclesCcCROSS
  195435. COUPLING REACTION BORONIC ACIDS DERIVATIVES ORGANOSTANNANES REAGENTS VINYL CHEMISTRY AGONIST M
  195436. 15188N
  195437. 2/28/96
  195438. ALSYNTHESIS OF 3
  195439. ALKYNYLPYRIDAZINES FROM 3
  195440. TRIFLUOROMETHANESULFONYLPYRIDAZINES
  195441. 1994X    1273
  195442. 1286Y
  195443. 14180
  195444. A    KOHRA, S.
  195445. Heterocycles
  195446. NITRILE YLIDES M
  195447. 15189N
  195448. 2/28/96
  195449. FLUORIDE ION PROMOTED AZOMETHINE YLID GENERATION FROM 1
  195450. METHYL
  195451. [METHYLTHIO (TRIMETHYLSILYLMETHYLIMINO)METHYLIMINO]
  195452. DIHYDROPYRIDINE, A SYNTHETIC EQUIVALENT OF AMINONITRILE YLID
  195453. 1994X    1217
  195454. 1220Y
  195455. 14181
  195456. SAROBE, M.
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  195458. (PG 89, 1994)M
  195459. 15190N
  195460. 2/28/96
  195461. AQPREPARATIVE FLASH VACUUM THERMOLYSIS. A SHORT SYNTHESIS OF CYCLOPENTA[C,D]PYRENE 
  195462. 1994X
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  195464. 14182
  195465. SHING, T. K. M.
  195466. J.C.S. Chem. Commun.K
  195467. (PG 449, 1994)M
  195468. 15191
  195469. 2/28/96
  195470. SELECTIVE SYNTHESES OF HOMOCHIRAL OXEPANES and TETRAHYDROPYRANS FROM CARBOHYDRATES VIA INTRAMOLECULAR NITRONE OR NITRILE OXIDE CYCLOADDITIONS 
  195471. 1994 X
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  195473. 14183
  195474. BANWELL, M. G.
  195475. J.C.S. Chem. Commun.K
  195476. (PG 591, 1994)M
  195477. 15192N
  195478. 2/28/96
  195479. AlREGIOCONTROLLED TOTAL SYNTHESIS OF IMERUBRINE 
  195480.  THE FIRST TOTAL SYNTHESIS OF A TROPOLOISOQUINOLINE ALKALOID 
  195481. 1994X
  195482. 1403Z
  195483. 14184
  195484. A    BOCHE, G.
  195485. J.C.S. Chem. Commun.CJSUBSTITUTED ORGANOLITHIUM COMPOUNDS LOW
  195486. TEMPERATURE C
  195487. NMR REAGENTS THF M
  195488. 15193N
  195489. 2/28/96
  195490. BROMO
  195491. [(BROMOMAGNESIUM)METHYLENE]FLUORENE
  195492. TETRAHYDROFURAN (1/4) STRUCTURE OF A MGBR/BR CARBENOID
  195493. 1994 X    1393
  195494. 1394Z
  195495. 14185
  195496. A    YUASA, Y.
  195497. J.C.S. Chem. Commun.C9BULGECININE (
  195498. BULGECININE CYCLIZATION DERIVATIVES ACID M
  195499. 15194N
  195500. 2/28/96
  195501. AjA NEW ROUTE to CHIRAL PYRROLIDINES VIA RADICAL CYCLISATION;  ENANTIOSELECTIVE SYNTHESIS OF (+)
  195502. BULGECININE
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  195505. 14186
  195506. MALHOTRA, R.
  195507. J.C.S. Chem. Commun.C:OXYGEN ATOM TRANSFER CARBONYL OXIDES NIH SHIFT OZONE C
  195508. 15195N
  195509. 2/28/96
  195510. OZONOLYSIS OF [60]FULLERENE
  195511. 1994X    1339
  195512. 1340Z
  195513. 14187
  195514. A    OZAWA, F.
  195515. J.C.S. Chem. Commun.CTMULTIPOINT CONTROL BICYCLIC ALKENES BICYCLO<2.2.1>HEPTANES PROSTAGLANDINS ARYLATION M
  195516. 15196N
  195517. 2/28/96
  195518. A>PALLADIUM
  195519. CATALYSED ASYMMETRIC HYDROALKENYLATION OF NORBORNENE
  195520. 1994 X    1323
  195521. 1324Z
  195522. 14188
  195523. PARK, S. B.
  195524. J.C.S. Chem. Commun.C4PORPHYRIN COMPLEXES HYDROSILYLATION KETONES OLEFINS M
  195525. 15197N
  195526. 2/28/96
  195527. TRIMETHYLSILYLCARBENE and BIS(TRIMETHYLSILYL) FORMALDEHYDE AZINE COMPLEXES OF CHIRAL BIS(4
  195528. ISOPROPYLOXAZOLINYL)PYRIDINE(DICHLORO)RUTHENIUM(II)
  195529. 1994X    1315
  195530. 1316Z
  195531. 14189
  195532. FRANCE, M. B.
  195533. J.C.S. Chem. Commun.C>RING
  195534. OPENING POLYMERIZATION RUTHENIUM CYCLOOLEFINS METATHESIS M
  195535. 15198N
  195536. 2/28/96
  195537. AiAN IRIDIUM
  195538. BASED CATALYST SYSTEM FOR METATHESIS/ISOMERIZATION OF ACYCLIC OLEFINS, INCLUDING METHYL OLEATE
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  195542. J.C.S. Chem. Commun.M
  195543. 15199N
  195544. 2/28/96
  195545. AGA SHORT STEREOSELECTIVE SYNTHESIS OF CIS
  195546.  and TRANS
  195547. HYDROXY
  195548. PROLINE
  195549. 1994 X
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  195551. 14191
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  195553. Collect. Czech. Chem. Commun.M
  195554. 15200N
  195555. 2/28/96
  195556. A;SYNTHESIS OF N
  195557. PHENYLSULFONYL PROTECTED FURO[3,2
  195558. B]PYRROLES
  195559. 1994X
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  195561. POPANDOVAYAMBOLIEVA, K.
  195562. Collect. Czech. Chem. Commun.M
  195563. 15201N
  195564. 2/28/96
  195565. SYNTHESIS OF NEW SPIROPYRROLIDINES and MICHAEL ADDITION PRODUCTS USING PHASE TRANSFER CATALYZED ADDITION OF SCHIFF BASES to 9
  195566. ARYLMETHYLENEFLUORENES
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  195569. AWAD, I. M. A.
  195570. Collect. Czech. Chem. Commun.M
  195571. 15202N
  195572. 2/28/96
  195573. AJSPIROHETEROCYCLIC SYSTEMS 
  195574.  NEW N
  195575. SUBSTITUTED SPIROHETEROCYCLIC NAPHTHENES
  195576. 1994 X
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  195581. 2/28/96
  195582. A!DERIVATIVES OF FURO[3,2
  195583. B]PYRROLE
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  195590. 2/28/96
  195591. DIELS
  195592. ALDER SELF
  195593. ADDITION AND RETROADDITION OF (CYCLOPENTADIENYLMETHYL)TRIETHOXYSILANE and SYNTHESIS OF ITS PERMETHYLATED ANALOGUE
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  195599. METHYLPHENYL)
  195600. TRIAZENE SOLVENTS METHANOL M
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  195603. AWKINETICS and MECHANISM OF ACID CATALYZED DECOMPOSITION OF 1
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  195610. MAGNETIC
  195611. RESONANCE SPECTROSCOPY MOLECULAR
  195612. ORBITAL CALCULATIONS CHEMICAL
  195613. SHIFTS WEAK ACIDS GAS
  195614. PHASE DISSOCIATION
  195615. CONSTANTS 4
  195616. SUBSTITUTED STYRENES CYANOCARBON ACIDS PROTON
  195617. TRANSFER CARBON ACIDS M
  195618. 15206N
  195619. 2/28/96
  195620. AOEFFECTS OF SUBSTITUENTS and MEDIUM ON ACIDITY OF A,A
  195621. BIS(BUTYLSULFONYL)TOLUENES
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  195626. DYES M
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  195628. 2/28/96V
  195629. NEW PYRAZOLINE DERIVATIVESW
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  195635. 2/28/96
  195636. AT3,5
  195637. BUTYL
  195638. BENZOQUINONE CLEAVES A CC
  195639. BOND IN VICINAL AMINOBENZYL ALCOHOLS
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  195645. 2/28/96
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  195654. ALDER REACTION CHEMICAL
  195655. REACTIVITY TOPOLOGICAL ASPECTS SUBSTITUTED ETHENES COPE REARRANGEMENT TRANSITION
  195656. STATES BUTADIENE RULES M
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  195659. AlTHE LEAST MOTION PRINCIPLE, CONCERTEDNESS and THE MECHANISMS OF PERICYCLIC REACTIONS 
  195660.  A SIMILARITY APPROACH
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  195666. CATALYZED
  195667. REACTIONS PI
  195668. ALLYLPALLADIUM COMPLEXES MODELING CHEMICAL
  195669. REACTIVITY SHIKIMATE
  195670. DERIVED METABOLITES PALLADIUM(0)
  195671. CATALYZED ALLYLIC SUBSTITUTION SUBSTRATE
  195672. CONTROLLED DIASTEREOSELECTIVITIES ALPHA,BETA
  195673. UNSATURATED CARBONYL
  195674. COMPOUNDS ORGANOSELENIUM
  195675. INDUCED CYCLIZATION OPTICALLY
  195676. ACTIVE ALLYLSILANES HYPOBROMOUS ACID ADDITION 
  195677. 15211N
  195678. 2/28/96
  195679. AbORGANIC REACTIVITY CONTROL BY MEANS OF NEIGHBORING GROUPS and ORGANOMETALLICS 
  195680.  A PERSONAL ACCOUNT
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  195688. DIAZOCARBONYL COMPOUNDS
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  195697. SILYLATION OF 2
  195698. ALKENENITRILES OR 3
  195699. ALKENENITRILES WITH IODOSILANES TRIETHYLAMINE AFFORDING 2
  195700. ALKENENITRILES OR 4
  195701. SILYL
  195702. ALKENENITRILES
  195703. 1994 X    1510
  195704. 1513Y
  195705. 14205
  195706. HOJO, M.
  195707. Bull. Chem. Soc. Jpn.M
  195708. 15214N
  195709. 2/28/96
  195710. REDUCTIVE CUPRATION OF CYANOKETENE DITHIOACETALS 
  195711.  GENERATION OF FUNCTIONALIZED (E)
  195712. VINYLCOPPER REAGENTS and THEIR REACTIONS WITH ELECTROPHILES
  195713. 1994 X    1495
  195714. 1498Y
  195715. 14206
  195716. Uno, H.B
  195717. Bull. Chem. Soc. Jpn.C ISOCYANIDES PORPHYRINS PYRROLES M
  195718. 15215N
  195719. 2/28/96
  195720. A NEW APPROACH to b
  195721. FLUOROPYRROLES BASED ON THE MICHAEL ADDITION OF ISOCYANOMETHYLIDE ANIONS to A
  195722. FLUOROALKENYL SULFONES and SULFOXIDES
  195723. 1994 X    1441
  195724. 1448Y
  195725. 14207
  195726. TANAKA, N.
  195727. Bull. Chem. Soc. Jpn.CeMETHOXYPHENYLALKENYL PHENANTHRENECARBOXYLATES PHOTOPHYSICAL BEHAVIOR EXCITED COMPLEXES CYCLOADDITION M
  195728. 15216N
  195729. 2/28/96
  195730. INTRAMOLECULAR PHOTOCYCLOADDITION OF (E)
  195731. METHOXYPHENYL)
  195732. PENTENYL 6
  195733. CYANO
  195734. PHENANTHRENECARBOXYLATE 
  195735.  TEMPERATURE and SOLVENT EFFECTS
  195736. 1994X    1434
  195737. 1440Y
  195738. 14208
  195739. A    SATOH, T.
  195740. Bull. Chem. Soc. Jpn.C>ORGANIC
  195741. SYNTHESIS ALPHA,BETA
  195742. EPOXY SULFOXIDES ARYL SULFOXIDES M
  195743. 15217N
  195744. 2/28/96
  195745. GENERATION OF THE A
  195746. SULFINYL CARBENOID FROM A
  195747. CHLORO SULFOXIDES 
  195748.  A NEW METHOD FOR ONE
  195749. CARBON HOMOLOGATION OF KETONES to A
  195750. SULFINYL KETONES
  195751. 1994X    1412
  195752. 1418Y
  195753. 14209
  195754. SRIVASTAVA, A.
  195755. Bull. Chem. Soc. Jpn.C9AMINE ADDITIONS ELECTRON PAIR KINETICS SULFONES BOND PMR M
  195756. 15218N
  195757. 2/28/96
  195758. A[STEREOCHEMISTRY OF THE ADDITION PRODUCT OF N
  195759. AMINOSUCCINIMIDE MOIETY to AN ACETYLENIC ESTER
  195760. 1994 X    1386
  195761. 1389Y
  195762. 14210
  195763. HERTWIG, R. H.
  195764. Angew. Chem. Int. Ed. Engl. M
  195765. 15219N
  195766. 2/28/96
  195767. INDACENE:  A DELOCALIZED, FORMALLY ANTIAROMATIC 12 p ELECTRON SYSTEM
  195768. 1994 X    1192
  195769. 1194Y
  195770. 14211
  195771. BURGESS, K.
  195772. Angew. Chem. Int. Ed. Engl. M
  195773. 15220N
  195774. 2/28/96
  195775. AfA REAGENT FOR DETERMINING OPTICAL PURITIES OF DIOLS BY FORMATION OF DIASTEREOMERIC ARYLBORONATE ESTERS
  195776. 1994 X    1182
  195777. 1184Y
  195778. 14212
  195779. A    BOCHE, G.
  195780. Angew. Chem. Int. Ed. Engl. M
  195781. 15221N
  195782. 2/28/96
  195783. THE OXENOID CHARACTER OF METALATED HYDROPEROXIDES O(M)OR:  OXIDATION OF ORGANOMETALLIC COMPOUNDS R'M' to R'OH UNDER MILD CONDITIONS
  195784. 1994 X    1161
  195785. 1163Y
  195786. 14213
  195787. Gut, I. G.B
  195788. Angew. Chem. Int. Ed. Engl. M
  195789. 15222N
  195790. 2/28/96
  195791. INDOLE
  195792. 1994 X    1153
  195793. 1156Y
  195794. 14214
  195795. BEIFUSS, U.
  195796. Angew. Chem. Int. Ed. Engl. M
  195797. 15223N
  195798. 2/28/96
  195799. A!NEW TOTAL SYNTHESES OF STRYCHNINE
  195800. 1994 X    1144
  195801. 1149Y
  195802. 14215
  195803. PIZZOTTI, M.
  195804. J.C.S. Perkin Trans. 2C)RU3(CO)12 NITROBENZENES CLUSTERS LIGANDS M
  195805. 15224N
  195806. 2/28/96
  195807. ROLE OF ALKALI HALIDES IN THE SYNTHESIS OF NITROGEN CONTAINING HETEROCYCLES BY REDUCTIVE CARBONYLATION OF AROMATIC NITRO
  195808. DERIVATIVES CATALYSED BY RU3(CO)12
  195809. 1994 X
  195810. 14216
  195811. HYNES, M. J.
  195812. J.C.S. Perkin Trans. 2C4CATALYSIS CYANOGEN ENOLIZATION COPPER(II) COMPLEXES M
  195813. 15225N
  195814. 2/28/96
  195815. REACTIONS OF b
  195816. KETOAMIDES .1. KINETICS OF ENOLISATION OF ACETOACETAMIDE IN WATER AND OF ACETOACETAMIDE and ACETOACETANILIDE IN ETHANOL
  195817. WATER
  195818. 1994 X
  195819. 14217
  195820. CHIN, W. S.
  195821. J.C.S. Perkin Trans. 2C]GROUND
  195822. STATES MOLECULES PHOTOELECTRON SPECTRA REARRANGEMENTS ISOMERIZATION ETHYLENE RADICALS M
  195823. 15226N
  195824. 2/28/96
  195825. A^THERMAL DECOMPOSITION OF THIIRANE and 2
  195826. METHYLTHIIRANE:  AN EXPERIMENTAL and THEORETICAL STUDY
  195827. 1994 X
  195828. 14218
  195829. JURANIC, I. O.
  195830. J.C.S. Perkin Trans. 2C
  195831. SN2 TRANSITION
  195832. STATES ABINITIO M
  195833. 15227N
  195834. 2/28/96
  195835. A>CYCLISATION OF ALKOXY RADICALS. A SEMIEMPIRICAL MNDO
  195836. PMS STUDY
  195837. 1994 X
  195838. 14219
  195839. JEEVARAJAN, A. S.
  195840. J.C.S. Perkin Trans. 2C
  195841. ELECTRON
  195842. PARAMAGNETIC RESONANCE TRANS BETA
  195843. CAROTENE CATION RADICALS MODEL PHOTOSYNTHESIS PHOTOCHEMISTRY IDENTIFICATION SPECTROSCOPY DICATIONS POLYENES M
  195844. 15228N
  195845. 2/28/96
  195846. A;GEOMETRICAL ISOMERIZATION OF CAROTENOIDS IN DICHLOROMETHANE
  195847. 1994 X
  195848. 14220
  195849. TAKEUCHI, H.
  195850. J.C.S. Perkin Trans. 2CcTRIFLUOROMETHANESULFONIC ACID TRIFLUOROACETIC
  195851. ACID HYDRAZOIC ACID AMINATION DERIVATIVES DISULFIDES M
  195852. 15229N
  195853. 2/28/96
  195854. AnNOVEL GENERATION OF ARYLSULFENIUM ION INTERMEDIATES and EFFICIENT AROMATIC ARYLTHIOLATION BY THE INTERMEDIATES
  195855. 1994X
  195856. 14221
  195857. ROGOWSKI, J.
  195858. J.C.S. Perkin Trans. 2CRDEPENDENT CHARGE DELOCALIZATION ABSORPTION
  195859. SPECTRA IONS OXIDATION STABILITY BONDS M
  195860. 15230N
  195861. 2/28/96
  195862. AWINTRAMOLECULAR INTERACTIONS BETWEEN SULFUR ATOMS IN CYCLOTETRATHIOETHER RADICAL CATIONS
  195863. 1994 X
  195864. 14222
  195865. COLOMBANI, D.
  195866. J.C.S. Perkin Trans. 2CvFREE
  195867. RADICAL ADDITIONS TERT
  195868. BUTYL PEROXIDE 2,3
  195869. EPOXY PROPANATION HETEROCYCLES DERIVATIVES THERMOLYSIS SOLVENTS ESTERS M
  195870. 15231N
  195871. 2/28/96
  195872. AsINTRAMOLECULAR HOMOLYTIC DISPLACEMENTS .2. POLAR EFFECTS IN THE HOMOLYTIC INDUCED DECOMPOSITIONS OF ALLYL PEROXIDES
  195873. 1994 X
  195874. 14223
  195875. TSENTALOVICH, Y. P.
  195876. J.C.S. Perkin Trans. 2C
  195877. ELECTRON
  195878. SPIN RESONANCE ABSOLUTE RATE CONSTANTS TERT
  195879. BUTYL RADICALS PHOTOCHEMICAL
  195880. REACTIONS TERMINATION KINETICS ABSORPTION
  195881. SPECTRA ALIPHATIC
  195882. KETONES DIBENZYL KETONES SELF
  195883. TERMINATION ROOM
  195884. TEMPERATURE M
  195885. 15232N
  195886. 2/28/96
  195887. AXSOLVENT EFFECT ON THE DECARBONYLATION OF ACYL RADICALS STUDIED BY LASER FLASH PHOTOLYSIS
  195888. 1994X
  195889. 14224
  195890. SHAPIRO, E. A.
  195891. J.C.S. Perkin Trans. 2C
  195892. CYCLOPROPANATION M
  195893. 15233N
  195894. 2/28/96
  195895. AcREGIOSELECTIVE RH2(OAC)4
  195896. PROMOTED REACTIONS OF METHYL DIAZOACETATE WITH TERMINAL TRIPLE BOND ENYNES
  195897. 1994 X
  195898. 14225
  195899. KIRBY, A. J.
  195900. J.C.S. Perkin Trans. 2C
  195901. VINYL ION REACTIVITY MECHANISM M
  195902. 15234N
  195903. 2/28/96
  195904. AuHIGHLY EFFICIENT INTRAMOLECULAR GENERAL ACID CATALYSIS OF ENOL ETHER HYDROLYSIS, WITH RAPID PROTON TRANSFER to CARBON
  195905. 1994X
  195906. 14226
  195907. ADEMBRI, G.
  195908. Tet. Lett.
  195909. C1CRYSTAL
  195910. STRUCTURE TETRAACETYLETHYLENE FUROFURANS K
  195911. REACTION OF 3,4
  195912. DIACETYL
  195913. HEXEN
  195914. DIONE, 1, WITH ALKYL OR ARYL PRIMARY AMINES. 2A
  195915. G, LED TO HIGHLY SUBSTITUTED 1H
  195916. PYRROL
  195917. 3(2H)
  195918. ONES, 3A
  195919. G. THE STRUCTURE WAS ESTABLISHED FROM A SINGLE CRYSTAL X
  195920. RAY ANALYSIS OF COMPOUND 3C.M
  195921. 15235N
  195922. 2/28/96
  195923. A6A NEW ROUTE to HIGHLY SUBSTITUTED 1H
  195924. PYRROL
  195925. 3(2H)
  195926. 1994 X    4023
  195927. 4026Y
  195928. 14227
  195929. DELGADO, A.
  195930. Tet. Lett.C
  195931. PALLADIUM
  195932. CATALYZED POLYCYCLIZATION ANION CAPTURE PROCESSES INTRAMOLECULAR CYCLIZATION TL(I) SALTS CYCLOADDITION RING DERIVATIVES DIENYNES ALKYNES HALIDES 
  195933. sREACTION OF DIFFERENT VINYL BROMIDES (1A
  195934. 3A), BEATING PHENYL SUBSTITUTED ALKENYLOXYALKYL GROUPS, WITH NI(CO)4 AFFORDS THE CORRESPONDING SUBSTITUTED CYCLIC ETHERS 1B
  195935. 3B IN MODERATE TO GOOD YIELDS AND HIGH DIASTEREOSELECTIVITY. IN THE CYCLIZATION OF 1A, THE STEREOSELECTIVITY OF THE PROCESS CAN BE REVERSED BY THE USE OF ADDITIVES, SUCH AS KOAC, TIOAC, CS2CO3, AND KOCOCF3.
  195936. 15236N
  195937. 2/28/96
  195938. AuSTEREOSELECTIVE SYNTHESIS OF TETRAHYDROFURANS and TETRAHYDROPYRANS BY NI(0) PROMOTED TANDEM CYCLIZATION
  195939. CARBONYLATION
  195940. 1994 X    4011
  195941. 4014Y
  195942. 14228
  195943. BARROS, M. T.
  195944. Tet. Lett.C"ORGANIC
  195945. SYNTHESIS (
  195946. QUINIC ACID 
  195947. QUINIC ACID IS CONVERTED STEREOSELECTIVELY INTO A COMMON CYCLOPENTANE INTERMEDIATE USEFUL FOR THE SYNTHESIS OF CARBOCYCLIC NUCLEOSIDES PROSTAGLANDINS AND OTHER IMPORTANT CYCLOPENTANE BASED COMPOUNDS.M
  195948. 15237N
  195949. 2/28/96
  195950. AKA FLEXIBLE SYNTHESIS OF SOME POLYSUBSTITUTED CYCLOPENTANES FROM QUINIC ACID
  195951. 1994 X    3999
  195952. 4002Y
  195953. 14229
  195954. CHIBALE, K.
  195955. Tet. Lett.C
  195956. PHENYLTHIO MIGRATION ASYMMETRIC
  195957. SYNTHESIS ENANTIOSELECTIVE SYNTHESIS KINETIC RESOLUTIONS ANTIALDOL REACTIONS KETONES SULFENYLATION ALKYLATION REDUCTION EPOXIDES 
  195958. OPTICALLY ACTIVE LINEAR AND BRANCHED CHAIN 2
  195959. PHENYLTHIO ALDEHYDES CAN BE MADE IN HIGH OPTICAL PURITY (UP TO >98% E.E.) BY SULFENYLATION OF A PHENYLALANINE
  195960. DERIVED OXAZOLIDINONE IMIDE, REDUCTION AND RE
  195961. OXIDATION WITH THE DESS
  195962. MARTIN REAGENT EVEN THOUGH THE PRODUCTS ENOLISE EASILY.
  195963. 15238N
  195964. 2/28/96
  195965. A8THE SYNTHESIS OF OPTICALLY ACTIVE 2
  195966. PHENYLTHIO ALDEHYDES
  195967. 1994 X    3991
  195968. 3994Y
  195969. 14230
  195970. A    MAITI, G.
  195971. Tet. Lett.C
  195972. LIGNAN (+/
  195973. DIHYDROSESAMIN ORGANIC
  195974. SYNTHESIS ANNULATION ROUTE CHAIN REACTIONS (+/
  195975. ISOGMELINOL (+/
  195976. PAULOWNIN NEOLIGNANS DESIGN K
  195977. A SHORT AND STEREOSELECTIVE SYNTHESIS OF (+/
  195978. DIHYDROSESAMIN 1 HAS BEEN ACHIEVED FROM 2 BY INTRAMOLECULAR RADICAL CYCLISATION REACTION IN GOOD OVERALL YIELD.M
  195979. 15239N
  195980. 2/28/96
  195981. A]SHORT and STEREOSELECTIVE SYNTHESIS OF (+/
  195982. DIHYDROSESAMIN BY A RADICAL CYCLISATION REACTION
  195983. 1994 X    3985
  195984. 3986Y
  195985. 14231
  195986. Woo, S. H.B
  195987. Tet. Lett.C2TETRAALKYLSTANNANES CYCLIZATION CHEMISTRY COMPLEX K
  195988. TREATMENT OF STANNYL ALDEHYDES 5A, 5B, AND KETONE 5C WITH MGBR2 AS THE LEWIS ACID CATALYST CAN INITIATE THE INTERNAL CLEAVAGE REACTIONS OF CARBON
  195989. TIN SIGMA BOND LEADING TO ALPHA
  195990. QUINODIMETHANES, WHICH CAN THEN UNDERGO DIELS 
  195991.  ALDER CYCLOADDITIONS.M
  195992. 15240N
  195993. 2/28/96
  195994. AULEWIS ACID
  195995. PROMOTED GENERATION OF A
  195996. QUINODIMETHANES and CYCLOADDITION REACTIONS
  195997. 1994X    3975
  195998. 3978Y
  195999. 14232
  196000. TAKAHASHI, Y.
  196001. Tet. Lett.C>TRANSFER PHOTOOXYGENATION COPE REARRANGEMENT MECHANISM OXYGEN 
  196002.  INTRAMOLECULAR [2 + 2] CYCLOADDITION OF 2,6
  196003. DIARYL
  196004. HEPTADIENES 1A
  196005. C TO BICYCLOHEPTANES 2 CAN BE INDUCED BY ELECTRON
  196006. TRANSFER PHOTOSENSITIZATION WITH 9,10
  196007. DICYANOANTHRACENE. A STEPWISE MECHANISM INVOLVING CYCLIC 1,4
  196008. CATION RADICAL 3 HAS BEEN PROPOSED BASED ON THE TRAPPING EXPERIMENTS.
  196009. 15241N
  196010. 2/28/96
  196011. AZELECTRON
  196012. TRANSFER INDUCED INTRAMOLECULAR [2+2] CYCLOADDITION OF 2,6
  196013. DIARYLHEPTA
  196014. DIENES
  196015. 1994 X    3953
  196016. 3956Y
  196017. 14233
  196018. STRZALKO, T.
  196019. Tet. Lett.
  196020. C"DERIVATIVES REACTIVITY CARBANIONS 
  196021. sA DIRECT EVIDENCE OF THE INFLUENCE OF AGGREGATION STATE OF LITHIATED PHENYLACETONITRILE 1 ON THE 1,2 VERSUS 1,4 REGIOSELECTIVITY TOWARDS BENZYLIDENEACETONE 2 WAS ESTABLISHED. PROGRESSIVE ADDITION OF HEXANE TO THF SOLUTIONS RAISED THE AGGREGATES PROPORTION OF 1 AS EVIDENCED BY IR V(CN) BAND AND LED TO AN INCREASE OF 1,4 ADDUCT MONOMERS AFFORDED 1,2 ADDITION IN PURE THF.
  196022. 15242N
  196023. 2/28/96
  196024. AjEFFECT OF AGGREGATION OF NITRILE ANIONS ON THE 1,2 VERSUS 1,4 REGIOSELECTIVITY TOWARDS BENZYLIDENEACETONE.
  196025. 1994X    3935
  196026. 3936Y
  196027. 14234
  196028. STREITH, J.
  196029. Tet. Lett.C:CHIRAL 1
  196030. METHOXYPYRIDINIUM SALTS ALKYLATION SERINE 
  196031. R PRONOUNCED ASYMMETRIC INDUCTION (DB. = 95 %) WAS OBSERVED DURING METHYLATION OF PYRIDINIUM SALT 7 WITH MEMGI WHICH LED ULTIMATELY TO (2R) 2
  196032. METHYL
  196033. DIHYDRO
  196034.  PYRIDONE 9. THIS RESULT IS BEST EXPLAINED BY ASSUMING CHELATE
  196035. CONTROL DURING THE ASYMMETRIC ALKYLATION STEP.
  196036. 15243N
  196037. 2/28/96
  196038. AFA SIMPLE ASYMMETRIC SYNTHESIS OF 2
  196039. SUBSTITUTED 2,3
  196040. DIHYDRO
  196041. PYRIDONES
  196042. 1994  X    3927
  196043. 3930Y
  196044. 14235
  196045. JEFFORD, C. W.
  196046. Tet. Lett.C
  196047. GLUTAMIC ESTER BORON TRIBROMIDE CATALYTIC HYDROGENATION 5.8
  196048. DISUBSTITUTED INDOLIZIDINE ACIDS 
  196049.  DIAZO KETONE PYRROLE RHODIUM INSERTION CH INSERTION CHIRAL ENANTIOSPECIFIC ASYMMETRIC INDUCTION
  196050. GLUTAMIC DIETHYL ESTER HYDROCHLORIDE WAS CONVERTED TO ITS PYRROLE DERIVATIVE 22 BY CONDENSATION WITH 2,5
  196051. DIMETHOXYTETRAHYDROFURAN IN WATER. CYCLIZATION OF 22 WITH BBR3 AFFORDED (5S)
  196052. DIHYDRO
  196053. ETHOXYCARBONYL
  196054. 8(7H)
  196055. INDOLIZINONE (23). CATALYTIC HYDROGENATION OF 23 OVER PD/C IN ACETIC ACID GAVE EXCLUSIVELY (5S,9R)
  196056. ETHOXYCARBONYL INDOLIZIDINE IN AN OVERALL YIELD OF 41%, WHEREAS HYDROGENATION OVER RH/AL2O3 IN ETHANOL GAVE PREDOMINANTLY (5S,8S,9S)
  196057. ETHOXYCARBONYL
  196058.  HYDROXYINDOLIZIDINE IB
  196059. N 48.5% OVERALL YIELD.
  196060. 15244N
  196061. 2/28/96
  196062. AYAN ENANTIOSPECIFIC ENTRY to INDOLIZIDINES BY INTRAMOLECULAR ACYLATION OF N
  196063. PYRROLE ESTERS
  196064. 1994 X    3905
  196065. 3908Y
  196066. 14236
  196067. ETTMAYER, P.
  196068. Tet. Lett.
  196069. SYNTHESES OF 2
  196070. SUBSTITUTED 1
  196071. HYDROXYETHYLENE BUILDING BLOCKS, USEFUL AS THE CENTRAL MOIETY OF HIV
  196072. 1 PROTEASE INHIBITORS, IS DESCRIBED. DILITHIATED N
  196073. PROTECTED
  196074. AMINO
  196075.  PHENYL BUTANOIC METHYL ESTERS ARE REACTED WITH ALDEHYDES TO GIVE PREDOMINANTLY ALDOL PRODUCTS WITH 1,U CONFIGURATION. THE DIASTEREOMERIC RATIO DEPENDS ON THE N
  196076. PROTECTING GROUP AND ON THE EXPERIMENTAL CONDITIONS. THE CONFIGURATIONS ARE ASSIGNED BY H
  196077. NMR OF CYCLIC DERIVATIVES AND ARE SUPPORTED BY X
  196078. RAY STRUCTURE.
  196079. 15245N
  196080. 2/28/96
  196081. A[ADDITION OF DILITHIATED METHYL
  196082. AMINOBUTANOATE to ALDEHYDES PROCEEDS WITH UL
  196083. INDUCTION
  196084. 1994X    3901
  196085. 3904Y
  196086. 14237
  196087. HARTKE, K.
  196088. Tet. Lett.
  196089. REACTIONS OF 3,5
  196090. DIARYL
  196091. DITHIOLIUM SALTS 1 WITH ALKALI CYCLOPENTADIENIDES 2 LEAD TO A SCISSION OF THE S,S
  196092. BOND FOLLOWED BY AN INTRAMOLECULAR DIELS ALDER ADDITION TO YIELD THE TRICYCLIC PRODUCTS 4. THESE REARRANGE READILY TO THE MORE STABLE ISOMERS 5.M
  196093. 15246N
  196094. 2/28/96
  196095. AYINTRAMOLECULAR DIELS ALDER ADDUCTS FROM 1,2
  196096. DITHIOLIUM SALTS and METAL CYCLOPENTADIENIDES
  196097. 1994X    3893
  196098. 3896Y
  196099. 14238
  196100. KALGUTKAR, R.
  196101. Tet. Lett.C
  196102. CRYSTALS DIAZIDE PAIRS K
  196103. PHOTOLYSIS OF STERICALLY HINDERED BIS(ARYLOXY)PHOSPHINE AZIDES IN SOLUTION, FROZEN MATRIX, OR NEAT SOLID STATES LEADS TO FACILE UNIMOLECUIAR PRODUCTION OF ARYLOXYL RADICALS.M
  196104. 15247N
  196105. 2/28/96
  196106. AcCONVENIENT UNIMOLECULAR SOURCES OF ARYLOXYL RADICALS .3. PHOTOLYSIS OF BIS(ARYLOXY)PHOSPHINE AZIDES
  196107. 1994 X    3889
  196108. 3892Y
  196109. 14239
  196110. GLASS, R. S.
  196111. Tet. Lett.C
  196112. ANTIBIOTIC SUBSTANCE LEINAMYCIN 1,3
  196113. DIOXO
  196114. DITHIOLANE MOIETY DIMETHYLDIOXIRANE DIOXIRANES CHEMISTRY SULFOXIDES STREPTOMYCES DERIVATIVES SULFIDES 
  196115. OXIDATION OF 1,2
  196116. DITHIOLAN
  196117. ONES 1 WITH ONE EQUIVALENT OF DIMETHYLDIOXIRANE IN DICHLOROMETHANE AT 
  196118. 78 DEGREES C PRODUCES THE CORRESPONDING 1,2
  196119. DITHIOLAN
  196120. ONE 1
  196121. OXIDES 2 IN HIGH YIELD AND WITH DIASTEREOSELECTIVITIES AS HIGH AS 18: 1. THE MAJOR DIASTEREOMER FORMED IS THE TRANS ISOMER. AN X
  196122. RAY CRYSTALLOGRAPHIC STRUCTURE STUDY OF THE MAJOR DIASTEREOMER 2C OBTAINED BY OXIDATION OF 1G IS REPORTED.
  196123. 15248N
  196124. 2/28/96
  196125. A@DIASTEREOSELECTIVE OXIDATION OF SUBSTITUTED 1,2
  196126. DITHIOLAN
  196127. 1994 X    3887
  196128. 3888Y
  196129. 14240
  196130. ZHANG, W.
  196131. Tet. Lett.
  196132. EXPANSION 7
  196133. MEMBERED HETEROCYCLES HALOGENATED KETENES BICYCLIC SYSTEMS GROUP MIGRATION REARRANGEMENT CONSTRUCTION CYCLOBUTANONES DICHLOROKETENE CYCLOADDITIONS 
  196134.  KETENE CHLORO CYCLOBUTANONE RADICAL TIN CARBONYL REARRANGEMENT ADDITION ALKOXY FRAGMENTATION RING OPENING
  196135. @STEREOSPECIFIC ANNULATION OF CYCLIC ALKENES FOR THE PREPARATION OF CIS
  196136. FUSED SEVEN
  196137. MEMBERED RING SYSTEMS WAS ACCOMPLISHED BY SEQUENTIAL [2 + 2] CYCLOADDITION, EXO
  196138. ALLYLATION, HYDROHALOGENATION, AND FREE RADICAL RING EXPANSION. THE NEW STRATEGY EXTENDS OUR RECENTLY DEVELOPED CYCLOBUTANONE
  196139. BASED RING EXPANSION REACTIONS.
  196140. 15249N
  196141. 2/28/96
  196142. AGFREE RADICAL
  196143. BASED ANNULATION OF ALKENES YIELDING FUSED CYCLOHEPTANONES
  196144. 1994 X    3865
  196145. 3868Y
  196146. 14241
  196147. SIEBURTH, S. M.
  196148. Tet. Lett.C-MOLECULAR MECHANICS FORCE
  196149. FIELD SYSTEM ROUTE 
  196150. INTRAMOLECULAR PHOTOCYCLOADDITION OF 2
  196151. PYRIDONES JOINED BY A FOUR
  196152. CARBON CHAIN WILL FORM THE FUSED 8
  196153. 6 RING SYSTEM OF TAXOL WITH BOTH OF THE QUATERNARY CARBONS. A C
  196154. 7 SILYLOXY GROUP ON THE TETHER FULLY CONTROLS STEREOGENESIS TO GIVE THE PHOTOPRODUCT AS A SINGLE ISOMER.
  196155. 15250N
  196156. 2/28/96
  196157. A1THE BC RINGS Of TAXOL BY [4+4] PHOTOCYCLOADDITION
  196158. 1994 X    3861
  196159. 3864Y
  196160. 14242
  196161. BASAVAIAH, D.
  196162. Tet. Lett.CeBAYLIS
  196163. HILLMAN REACTION ALDEHYDES ACRYLATES ESTER ALPHA 
  196164. CHIRAL QUATERNARY CARBON TERPENE DIELS
  196165. ALDERK
  196166. CHIRAL MIKANECIC ACID (1) WAS SYNTHESIZED IN 74% ENANTIOMERIC PURITY (92% EE AFTER CRYSTALLIZATION) VIA ASYMMETRIC DIELS
  196167. ALDER REACTION OF A NOVEL IN SITU GENERATED CHIRAL 1,3
  196168. BUTADIENE
  196169. CARBOXYLATE (A).M
  196170. 15251N
  196171. 2/28/96
  196172. FIRST ENANTIOSELECTIVE SYNTHESIS OF MIKANECIC ACID VIA DIELS
  196173. ALDER CYCLOADDITION MEDIATED CONSTRUCTION OF CHIRAL VINYLIC QUATERNARY CENTER
  196174. 1994 X    4227
  196175. 4230Y
  196176. 14243
  196177. PRAKASH, O.
  196178. Tet. Lett.C
  196179. ALKENES
  196180. HYPERVALENT IODINE OXIDATION OF 2
  196181. METHYL
  196182. QUINOLONES USING [HYDROXY(TOSYLOXY)IODO] BENZENE AFFORDED 2
  196183. METHYL
  196184. PHENOXYQUINOLINES WITH THE INTERMEDIACY OF ALPHA
  196185. PHENYLIODONIO TOSYLATES AND NOVEL MONOCARBONYL IODONIUM YLIDES.M
  196186. 15252N
  196187. 2/28/96
  196188. HYPERVALENT IODINE OXIDATION OF 2
  196189. METHYL
  196190. QUINOLONES USING [HYDROXY(TOSYLOXY)IODO] BENZENE:  SYNTHESIS OF 2
  196191. METHYL
  196192. PHENOXYQUINOLINES VIA NOVEL MONOCARBONYL IODONIUM YLIDES
  196193. 1994 X    4211
  196194. 4214Y
  196195. 14244
  196196. LOHRAY, B. B.
  196197. Tet. Lett.
  196198. 1 NMR STUDIES ON BIS(9
  196199. DIHYDROQUINIDINYL)TEREPHTHALATE (DHQD(2)
  196200. TP) WITH VARIOUS CONCENTRATIONS OF OSMIUM TETROXIDE AND TRANS
  196201. HEXENE REVEAL THAT OSO4 IS BOUND TO BOTH THE QUINUCLIDINE MOIETIES OF DHQD(2)
  196202. TP BUT ONLY ONE OR THE BOUND OSO4 REACTS WITH ALKENES IN THE AD PROCESS.
  196203. 15253N
  196204. 2/28/96
  196205. A>ON THE MECHANISM OF ASYMMETRIC DIHYDROXYLATION (AD) OF ALKENES
  196206. 1994 X    4209
  196207. 4210Y
  196208. 14245
  196209. BEDDOES, R. L.
  196210. Tet. Lett.K\THE ALDOL REACTIONS AND SUBSEQUENT TRANSMETALLATION OF BETA
  196211. STANNYLPROPIONATES IS DESCRIBED.M
  196212. 15254N
  196213. 2/28/96
  196214. A\ALDOL REACTIONS OF METHYL (2
  196215. TRIBUTYLSTANNYL)TETRAHYDROFURAN
  196216. YLCARBOXYLATE LITHIUM ENOLATE
  196217. 1994 X    4189
  196218. 4192Y
  196219. 14246
  196220. ZHAO, Y. K.
  196221. Tet. Lett.KVA STEREOSELECTIVE SYNTHESIS OF 2,3,3 
  196222. TRIFUNCTIONALISED TETRAHYDROFURANS IS DESCRIBED.M
  196223. 15255N
  196224. 2/28/96
  196225. STEREOSELECTIVE ALKYLATION OF METHYL (2
  196226. TRIBUTYLSTANNYL)TETRAHYDROFURAN
  196227. YLCARBOXYLATE LITHIUM ENOLATE:  ACCESS to 2,3,3
  196228. TRISUBSTITUTED TETRAHYDROFURANS
  196229. 1994X    4187
  196230. 4188Y
  196231. 14247
  196232. ZHAO, Y. K.
  196233. Tet. Lett.C
  196234. ORGANIC
  196235. SYNTHESIS 
  196236. A STEREOSPECIFIC SYNTHESIS OF 2,3
  196237. DIFUNCTIONALISED TETRAHYDROFURANS VIA A TRANSMETALLATION
  196238.  ALKYLATION SEQUENCE OF THE CORRESPONDING 2
  196239. BUTYLSTANNYL)TETRAHYDROFURANS IS DESCRIBED.M
  196240. 15256N
  196241. 2/28/96
  196242. AKA STEREOSPECIFIC SYNTHESIS OF 2,3
  196243. DISUBSTITUTED TETRAHYDROFURAN DERIVATIVES
  196244. 1994X    4183
  196245. 4186Y
  196246. 14248
  196247. ZHAO, Y. K.
  196248. Tet. Lett.C/CONFIGURATIONAL STABILITY GENERATION INVERSION KFTHE IONIC REDUCTION OF A VARIETY OF BETA
  196249. STANNYLACRYLATES IS REPORTED.M
  196250. 15257N
  196251. 2/28/96
  196252. A&THE IONIC REDUCTION OF VINYL STANNANES
  196253. 1994 X    4179
  196254. 4182Y
  196255. 14249
  196256. Lee, I. Y. C.B
  196257. Tet. Lett.
  196258. CfSTEREOCHEMICAL CONTROL HEX
  196259. ENYL 
  196260.  RADICAL CYCLIZATION CYCLOPENTANOIDS TANDEM MICHAEL ALDOL PHOTOCHEMK
  196261. PHOTOCHEMICAL INITIATION OF RADICAL CYCLIZATION OF ALDOL CONDENSATION PRODUCTS EMPLOYING SIMPLE FLOOD LAMP GAVE VARIOUS BICYCLIC CARBOCYCLES.M
  196262. 15258N
  196263. 2/28/96
  196264. AcA CONVENIENT METHOD FOR THE RADICAL CYCLIZATION OF THE ALDOL PRODUCTS to FUSED BICYCLIC CARBOCYCLES
  196265. 1994 X    4173
  196266. 4174Y
  196267. 14250
  196268. KAMOCHI, Y.
  196269. Tet. Lett.C#ORGANIC
  196270. SYNTHESIS CARBOXYLIC
  196271. ACIDS 
  196272. DPHENOL WAS RAPIDLY REDUCED WITH SAMARIUM DIIODIDE
  196273. BASE SYSTEM IN THE PRESENCE OF PROTIC SOLVENT AT ROOM TEMPERATURE TO AFFORD 3
  196274. CYCLOHEXEN
  196275. OL ACCOMPANIED BY CYCLOHEXANOL. THE SIMILAR REDUCTION OF 4
  196276. METHOXYPHENOL AND 2
  196277. NAPHTHOL GAVE 4
  196278. HYDROXYCYCLOHEXANONE AND 1,2,3,4
  196279. TETRAHYDRO
  196280. NAPHTHOL IN EXCELLENT YIELD, RESPECTIVELY.
  196281. 15259N
  196282. 2/28/96
  196283. ASNOVEL and FACILE REDUCTION OF PHENOL DERIVATIVES WITH SAMARIUM DIIODIDE
  196284. BASE SYSTEM
  196285. 1994 X    4169
  196286. 4172Y
  196287. 14251
  196288. CHOU, T. C.
  196289. Tet. Lett.C
  196290. CAGE COMPOUNDS SYSTEMS 
  196291. FACIALLY DISSYMMETRIC MALEIC ANHYDRIDE 1 IS SYNTHESIZED AND UNDERGOES DIELS
  196292. ALDER CYCLOADDITIONS WITH CYCLIC DIENES EXCLUSIVELY ON THE FACE SYN TO ITS ETHENO
  196293. BRIDGES.M
  196294. 15260N
  196295. 2/28/96
  196296. AsSYNTHESIS and DIELS
  196297. ALDER REACTIONS OF A FACIALLY DISSYMMETRIC TETRACYCLO
  196298. FUSED MALEIC ANHYDRIDE WITH CYCLIC DIENES
  196299. 1994 X    4165
  196300. 4168Y
  196301. 14252
  196302. Ono, K.B
  196303. Tet. Lett.C
  196304. VINYL SUBSTITUTION
  196305. REACTIONS ARYL HALIDES STEREOCONTROLLED SYNTHESIS UNSATURATED ALCOHOLS CONVENIENT SYNTHESIS CONJUGATED DIENOLS ORGANIC HALIDES ALDEHYDES KETONES K
  196306. ALKYL O
  196307. CINNAMYL CARBAMATES (3) WERE PREPARED IN GOOD YIELDS BY PALLADIUM CATALYZED ARYLATION OF N
  196308. ALKYL O
  196309. ALLYL CARBAMATES (2) WITH ARYL IODIDES.M
  196310. 15261N
  196311. 2/28/96
  196312. AoPALLADIUM CATALYZED ARYLATION OF N
  196313. ALKYL O
  196314. ALLYL CARBAMATES:  SYNTHESIS OF CINNAMYL ALCOHOLS VIA HECK ARYLATION
  196315. 1994 X    4133
  196316. 4136Y
  196317. 14253
  196318. TANAKA, T.
  196319. IWATA 
  196320. Tet. Lett.C
  196321. CHAMIGRANE
  196322. TYPE BROMINATED SESQUITERPENE (+/
  196323. (BROMOMETHYLENE)
  196324. 1,5,5
  196325.  TRIMETHYLSPIRO<5.5>UNDECA
  196326. ONE SPIROANNULATION CONSTRUCTION ANNULATION KETONES 
  196327. SPIRO CENTER SPIROANNELATION NATURAL PRODUCT INTRODUCTION ACETAL LEWIS ACID ENOL ETHER
  196328. SPIRO[5.5]UNDECANE DERIVATIVES 6A AND 7S WERE OBTAINED IN MODERATE STEREOSELECTIVITY BY THE INTRAMOLECULAR SPIROANNELATION REACTION OF A BIS
  196329. ACETAL 3 PROMOTED BY TMSOTF AND THE SELECTIVITY WAS REVERSED BY CHANGING THE SOLVENT FROM ACETONITRILE TO THF.M
  196330. 15262N
  196331. 2/28/96
  196332. AnA NOVEL and STEREOSELECTIVE SPIROANNELATION:  A FACILE ACCESS to APHIDICOLANE and STEMODANE B/C/D
  196333. RING SYSTEMS
  196334. 1994 X    4125
  196335. 4128Y
  196336. 14254
  196337. TAKAHATA, H.
  196338. Tet. Lett.
  196339. -A NEW ENVY TO CHIRAL BUTENOLIDE SYNTHONS STARTING WITH IODOLACTONIZATION OF THE READILY AVAILABLE, HOMOCHIRAL N
  196340. BENZYL
  196341. METHYL
  196342. HYDROXY
  196343. PENTENAMID (1) AND ITS APPLICATION TO THE SYNTHESES OF (+)
  196344. NEPHROSTERANIC ACID (5), (+)
  196345. TRANS
  196346. WHISKY LACTONE (6), AND (+)
  196347. TRANS
  196348. COGNAC LACTONE (7) ARE DESCRIBED.
  196349. 15263N
  196350. 2/28/96
  196351. NEW ENTRY to CHIRAL BUTENOLIDE SYNTHONS. APPLICATION TO EXPEDITIOUS SYNTHESES OF (+)
  196352. NEPHROSTERANIC ACID, (+)
  196353. TRANS
  196354. WHISKY LACTONE, and (+)
  196355. TRANS
  196356. COGNAC LACTONE
  196357. 1994 X    4123
  196358. 4124Y
  196359. 14255
  196360. Cho, B. T. B
  196361. Tet. Lett.C)TITANIUM
  196362. CARBOHYDRATE COMPLEXES REAGENTS 
  196363. THE ENANTIOSELECTIVE ADDITION OF DIETHYLZINC TO ALDEHYDES USING 1,2
  196364. ISOPROPYLIDENE
  196365.  DEOXY
  196366. DIALKYLAMINO
  196367. ALPHA
  196368. XYLOFURANOSES DERIVED FROM ALPHA
  196369. XYLOSE AS NEW CATALYSTS PROVIDED THE CORRESPONDING ALCOHLOS WITH 75
  196370. 96% EE.M
  196371. 15264N
  196372. 2/28/96
  196373. A{ENANTIOSELECTIVE ADDITION OF DIETHYLZINC to ALDEHYDES USING g
  196374. AMINOALCOHOLS DERIVED FROM A
  196375. XYLOSE AS NEW CHIRAL CATALYSTS
  196376. 1994 X    4115
  196377. 4118Y
  196378. 14256
  196379. KANEKO, Y.
  196380. Tet. Lett.
  196381. ENANTIOSELECTIVITY SYN
  196382. DIOL ASYMMETRIC ALDOL REACTION CHIRAL BORANE BETA
  196383. HYDROXY KETONES STEREOSELECTIVE REDUCTION KETENE ACETALS 1,3
  196384. DIOLS K
  196385. A STOICHIOMETRIC AMOUNT OF THE CHIRAL BORANE 1 TURNED OUT TO SUCCESSIVELY PROMOTE THE ASYMMETRIC ALDOL REACTION OF ALDEHYDES WITH ENOL SILYL ETHERS AND THE FOLLOWING ASYMMETRIC REDUCTION IN ONE POT TO AFFORD SYN
  196386. DIOLS WITH HIGH ENANTIOSELECTIVITY.M
  196387. 15265N
  196388. 2/28/96
  196389. DIRECT ENANTIOSELECTIVE SYNTHESIS OF SYN
  196390. DIOLS BY THE REACTION OF ALDEHYDES WITH ENOL SILYL ETHERS IN THE PRESENCE OF A CHIRAL BORANE COMPLEX. SUCCESSIVE ASYMMETRIC ALDOL REACTION and ASYMMETRIC REDUCTION WITH ONE PROMOTER
  196391. 1994X    4107
  196392. 4110Y
  196393. 14257
  196394. PAPAMICAEL, C.
  196395. Tet. Lett.C
  196396. METALATION REAGENTS LITHIUM 
  196397. STHE SYNTHESIS OF NEW 3
  196398. SUBSTITUTED ALPHA
  196399. CARBOLINES IS DESCRIBED AND THESE PRODUCTS WERE SUBJECTED TO ORTHO
  196400. LITHIATION EXPERIMENTS. 3
  196401. PIVALAMIDO AND 3
  196402. CARBOXAMIDO DERIVATIVES ARE CLEANLY LITHIATED AT 4
  196403. POSITION. THE RESULTS ARE CORRELATED WITH MNDO CALCULATIONS. VARIOUS 3,4
  196404. DISUBSTITUTED ALPHA
  196405. CARBOLINES ARE OBTAINED IN EXCELLENT YIELDS.
  196406. 15266N
  196407. 2/28/96
  196408. AdSTUDY OF THE LITHIATION OF 3
  196409. SUBSTITUTED A
  196410. CARBOLINES 
  196411.  A NEW ROUTE to 3,4
  196412. DISUBSTITUTED DERIVATIVES
  196413. 1994X    4099
  196414. 4102Y
  196415. 14258
  196416. A    ALBER, F.
  196417. Tet. Lett.
  196418. pTHE REACTION OF 1
  196419. BROMO
  196420. CHLOROMETHYL
  196421. METHYLTRICYCLO[4.1.0.0(2,7)]HEPTANE WITH METHYLLITHIUM LEADS TO EITHER 2
  196422. METHYL
  196423. METHYLENETRICYCLO[4.1.0.0(2,7)]HEPTANE OR 7
  196424. BROMO
  196425. DIMETHYL
  196426. METHYLENEBICYCLO[4.1.0]HEPTANE DEPENDING ON THE METHYLLITHIUM REAGENT USED. BOTH PRODUCTS SUGGEST THAT 6
  196427. METHYLTETRACYCLO[4.2.0.0(1,7). 0(5,7)]OCTANE WAS FORMED AS AN INTERMEDIATE.
  196428. 15267N
  196429. 2/28/96
  196430. METHYLTETRACYCLO[4.2.0.0(1,7).0(5,7)]OCTANE 
  196431.  A BRIDGED [3.3.3]FENESTRANE
  196432. 1994 X    4093
  196433. 4096Y
  196434. 14259
  196435. BHATT, R. K.
  196436. Tet. Lett.
  196437. (C^STANNYLHYDRIN TIN CHIRAL INDUCTION TRIMETHYL(TRIBUTYLSTANNYL)SILANE ORGANIC
  196438. SYNTHESIS REAGENTS
  196439. +ALDEHYDES, BUT NOT KETONES, ARE CONVERTED TO ALPHA
  196440. HYDROXYSTANNANES VIA THE CORRESPONDING SILYL ETHERS IN GOOD TO EXCELLENT YIELDS BY BU(4)NCN CATALYZED ADDITION OF BU(3)SNSIME(3) AND HYDROLYTIC ISOLATION. MODEST ASYMMETRIC INDUCTION WAS OBSERVED USING A CHIRAL QUATERNARY AMMONIUM CYANIDE CATALYST.
  196441. 15268N
  196442. 2/28/96
  196443. ATCONVENIENT PREPARATION OF A
  196444. TRIMETHYLSILYLOXY
  196445.  and A
  196446. HYDROXYSTANNANES FROM ALDEHYDES
  196447. 1994X    4081
  196448. 4084Y
  196449. 14260
  196450. SNIECKUS, V.
  196451. Tet. Lett.C
  196452. CONFIGURATIONAL STABILITY ALPHA
  196453. AMINOORGANOLITHIUMS NITROGEN ALKYLATION METALATION EQUIVALENT EXCHANGE 
  196454.  AMIDE LITHIATION CHELATE METHYL ALKYLATION SNIECKUS REGIOSELECTIVE
  196455. THE REGIOSELECTIVE LITHIATION AND FUNCTIONALIZATION AT THE N
  196456. METHYL GROUP OF N
  196457. METHYLALKYLAMINES 3 AND 5 ARE SHOWN WITH A VARIETY OF ELECTROPHILES TO GIVE PRODUCTS 4 AND 6, RESPECTIVELY, THUS PROVIDING A CONVENIENT METHODOLOGY FOR THE ELABORATION OF UNSYMMETRICAL AMINES.
  196458. 15269N
  196459. 2/28/96
  196460. AqREGIOSELECTIVE N
  196461. METHYL CARBON LITHIATION OF N
  196462. METHYLALKYLAMINES. EXPEDIENT SYNTHESIS OF UNSYMMETRICAL AMINES
  196463. 1994X    4067
  196464. 4070Y
  196465. 14261
  196466. TROST, B. M.
  196467. Tet. Lett.
  196468. SPONGE DISCODERMIA
  196469. CALYX CALYCULIN
  196470. A STEREOCONTROLLED SYNTHESIS CONSTRUCTION UNIT METABOLITES INHIBITORS FRAGMENT ALCOHOLS ACID K
  196471. USING A RU CATALYZED CYCLIZATION
  196472. ADDITION, A SHORT SYNTHESIS OF THE SPIROKETAL CORE CORRESPONDING TO THE NATURAL ENANTIOMER OF (
  196473. CALYCULIN A FROM R
  196474. PANTOLACTONE EMERGES.M
  196475. 15270N
  196476. 2/28/96
  196477. A8A SYNTHESIS OF THE SPIROKETAL SUBUNIT OF (
  196478. CALYCULIN A
  196479. 1994 X    4059
  196480. 4062Y
  196481. 14262
  196482. CABIDDU, S.
  196483. TetrahedronC(ALLENES BENZENETHIOL ALLYL RADICALS EPR 
  196484. THE RADICAL
  196485. CHAIN ADDITION REACTION OF BENZENETHIOL TO ALLENIC ESTERS HAS BEEN EXAMINED. THE REACTION PRODUCTS HAVE BEEN SEPARATED AND IDENTIFIED BY MEANS OF H
  196486. 1 NMR AND MASS SPECTROMETRY, AND THE RADICAL INTERMEDIATES DETECTED BY EPR SPECTROSCOPY.M
  196487. 15271N
  196488. 2/28/96
  196489. ARRADICAL
  196490. CHAIN ADDITION OF BENZENETHIOL to ALLENIC ESTERS 
  196491.  EPR and PRODUCT STUDIES
  196492. 1994X    4001
  196493. 4008Y
  196494. 14263
  196495. METZ, P.
  196496. TetrahedronCFREDUCTIVE ALKYLATION DIASTEREOSELECTION VINYLSILANES INDUCTION ESTERS 
  196497. DEPROTONATION AND SUBSEQUENT N
  196498. SILYLATION OF ALLYL N
  196499. PHENYLIMIDATES 1 LEAD TO N
  196500. SILYL KETENE N,O
  196501. ACETALS 5 WHICH UNDERGO A CLAISEN REARRANGEMENT TO YIELD GAMMA,DELTA
  196502.  UNSATURATED ANILIDES 3 AFTER HYDROLYTIC WORK
  196503. UP. THE TEMPERATURE FOR THE REARRANGEMENT STEP IS DEPENDENT ON THE NATURE OF THE SUBSTITUENT R2 IN S. KETENE ACETALS S WITH R2 = H REARRANGE READILY AT ROOM TEMPERATURE, WHILE HEATING AT 130
  196504. DEGREES
  196505. C IS REQUIRED IF R2 NOT
  196506. EQUAL H.  THE DEGREE OF SIMPLE DIASTEREOSELECTION ATTAINABLBBE FOR THE CONVERSION OF 1 TO 3 IS STRONGLY AFFECTED BY THE SIZE OF
  196507. 15272N
  196508. 2/28/96
  196509. AYCLAISEN REARRANGEMENT OF N
  196510. SILYL KETENE N,O
  196511. ACETALS GENERATED FROM ALLYL N
  196512. PHENYLIMIDATES
  196513. 1994X    3951
  196514. 3966Y
  196515. 14264
  196516. AURICH, H. G.
  196517. TetrahedronC
  196518. CYCLO
  196519. ADDITIONS 1,3
  196520. DIPOLAR CYCLOADDITION CARBOCYCLIC COMPOUNDS AMINO
  196521. ACIDS MONOSACCHARIDES TRANSFORMATIONS ALCOHOLS SERIES SUBSTITUTION DERIVATIVES 
  196522. STARTING FROM CHIRAL MERCAPTO ALCOHOLS 5 IN SEVERAL REACTION STEPS NITRONES 7 WERE FORMED WHICH UNDERWENT SPONTANEOUSLY INTRAMOLECULAR CYCLOADDITION TO GIVE DIASTEREOMERICALLY PURE PRODUCTS 8. HOWEVER, DURING THE REACTION COURSE PARTIAL RACEMIZATION HAD OCCURRED. IN CONTRAST, NITRONES 9 IN WHICH THE CHIRAL CENTER IS ADJACENT TO THE NITROGEN ATOM AFFORDED A MIXTURE OF THE TWO DIASTEREOMERIC CYCLOADDUCTS 10 AND 11. COMPOUND 14 WAS SYNTHESIZED FROM THE HOMOCHIRAL AMINO DIOL 12 WITH RETENTION B.OF CONFIGURATION AT THE TWO CHIRAL CENTERS. 14
  196523. 15273N
  196524. 2/28/96
  196525. AxHIGHLY DIASTEREOSELECTIVE FORMATION OF BICYCLIC COMPOUNDS BY INTRAMOLECULAR CYCLOADDITION OF CHIRAL THIAALKENYL NITRONES
  196526. 1994 X    3929
  196527. 3942Y
  196528. 14265
  196529. A    SAITO, N.
  196530. TetrahedronCgSELENIUM OXIDE OXIDATION ETHERS HEXAHYDRO
  196531. IMINO
  196532. BENZAZOCIN
  196533. DIONE DEMETHYLATION PHENOLS ACID 
  196534. 1,2,3,4,5,6
  196535. HEXAHYDRO
  196536. HYDROXY
  196537. IMINO
  196538. METHOXY
  196539. 3,8,11
  196540. TRIMETHYL
  196541. BENZAZOCINE 3B EMBODYING ALL OF THE SKELETAL FEATURES OF THE ABC RING OF SAFRACINS HAS BEEN SYNTHESIZED FROM COMPOUND 4A VIA A DIRECT REGIOSELECTIVE BROMINATION, FOLLOWED BY THE SEQUENCE REDUCTION, METAL
  196542. HALOGEN INTERCHANGE, AND REACTION OF THE ORGANOMETALLIC INTERMEDIATE WITH NITROBENZENE. AND THE CONVERSION OF 3B TO A QUINONE 21B IS ALSO DESCRIBED.
  196543. 15274N
  196544. 2/28/96
  196545. APSYNTHESIS OF SAFRAMYCINS .9. AN EFFICIENT SYNTHESIS OF THE ABC RING OF SAFRACINS
  196546. 1994X    3915
  196547. 3928Y
  196548. 14266
  196549. MORIYA, T.
  196550. SynlettK
  196551. (PG 149, 1994)M
  196552. 15275N
  196553. 2/28/96
  196554. SYNTHESIS OF ALLENES BY PALLADIUM
  196555. CATALYZED CROSS
  196556. COUPLING REACTION OF ORGANOBORON COMPOUNDS WITH PROPARGYLIC CARBONATES 
  196557.  TRANSMETALLATION OF ORGANOBORON COMPOUNDS WITH (ALKOXO)PALLADIUM COMPLEXES UNDER NEUTRAL CONDITIONS 
  196558. 1994 X
  196559. 14267
  196560. SAKURABA, S.
  196561. Synlett
  196562. ASYMMETRIC HECK REACTION CHIRAL AMINO PHOSPHINE DECALIN DERIVATIVES ORGANIC HALIDES METAL
  196563. COMPLEXES CARBON CENTERS ARYLATION OLEFINS HYDROGENATION 2,3
  196564. DIHYDROFURAN M
  196565. 15276N
  196566. 2/28/96
  196567. ASYMMETRIC HECK
  196568. TYPE HYDROARYLATION OF NORBORNENE WITH PHENYL TRIFLATE CATALYZED BY PALLADIUM COMPLEXES OF CHIRAL b
  196569. SULFONYLAMINOALKYL)PHOSPHINES
  196570. 1994X
  196571. 14268
  196572. A    NAGAI, H.
  196573. SynlettC
  196574. CHIRAL LIGANDS LIPASE (2R,5R)
  196575. HEXANEDIOL CYCLIC SULFATE ENANTIOSELECTIVE HYDROGENATION REACTIONS C2
  196576. SYMMETRICAL BIS(PHOSPHOLANES) ASYMMETRIC HYDROGENATION VERSATILE APPROACH BETA
  196577. LACTAMS HYDROLYSIS RESOLUTION M
  196578. 15277
  196579. 2/28/96
  196580. FACILE ENZYMATIC SYNTHESIS OF OPTICALLY ACTIVE 2,5
  196581. HEXANEDIOL DERIVATIVES and ITS APPLICATION to THE PREPARATION OF OPTICALLY PURE CYCLIC SULFATE FOR CHIRAL LIGANDS
  196582. 1994 X
  196583. 14269
  196584. DEKIMPE, N.
  196585. SynlettCo2
  196586. (BROMOMETHYL)AZIRIDINES ALLYLAMINES RADICAL
  196587. INDUCED RING OPENING AMINYLRADICALS (2
  196588. AZIRIDINYL)METHYLRADICALS M
  196589. 15278N
  196590. 2/28/96
  196591. A9RADICAL
  196592. INDUCED RING OPENING OF 2
  196593. (BROMOMETHYL)AZIRIDINES
  196594. 1994X
  196595. 14270
  196596. A    SAITO, S.
  196597. SynlettC
  196598. CHIRAL NITRONE [3+2] CYCLOADDITION VICINAL DIOL CONTROLLER DIASTEREOSELECTION STEREOSELECTIVE SYNTHESIS MICHAEL ADDITION TARTARIC ACID DERIVATIVES ROUTE SELECTIVITY M
  196599. 15279N
  196600. 2/28/96
  196601. CHIRAL ACYCLIC NITRONE BEARING PROTECTED VICINAL DIOL CONTROLLER PROVIDING SINGLE p (C=N)
  196602. FACE IN [3+2] CYCLOADDITION REACTIONS
  196603. 1994 X
  196604. 14271
  196605. A    SAITO, S.
  196606. SynlettCkCHIRAL DIOL OLEFIN NITRONE [3+2] CYCLOADDITION VICINAL DIOL CONTROLLER DIASTEREOSELECTION DERIVATIVES ACID M
  196607. 15280N
  196608. 2/28/96
  196609. AzROLE OF VICINAL DIOL CONTROLLER IN DISCRIMINATING p (C=C)
  196610. FACES OF DIPOLAROPHILE IN NITRONE OLEFIN CYCLOADDITION REACTIONS
  196611. 1994X
  196612. 14272
  196613. AKIYAMA, T.
  196614. SynlettC
  196615. ALPHA
  196616. KETO ESTER L
  196617. QUEBRACHITOL ALDOL REACTION CYCLITOL ASYMMETRIC SYNTHESIS HIGHLY ENANTIOSELECTIVE SYNTHESIS D
  196618. INOSITOL L
  196619. QUEBRACHITOL ABSOLUTE
  196620. CONFIGURATION DERIVATIVES M
  196621. 15281N
  196622. 2/28/96
  196623. ASYMMETRIC SYNTHESIS OF FUNCTIONALIZED TERTIARY ALCOHOLS BY DIASTEREOSELECTIVE ALDOL REACTION OF SILYL ENOL ETHER and KETENE SILYL ACETAL WITH A
  196624. KETO ESTERS BEARING AN OPTICALLY ACTIVE CYCLITOL AS A CHIRAL AUXILIARY
  196625. 1994X
  196626. 14273
  196627. HUVAL, C. C.
  196628. SynlettC|ANNULATION RADICAL ALKENE METHYLENECYCLOPROPANE METHYLENECYCLOPENTANE ATOM TRANSFER ADDITION SUBSTITUTED VINYLCYCLOPROPANES M
  196629. 15282N
  196630. 2/28/96
  196631. AVFREE
  196632. RADICAL MEDIATED [3+2] METHYLENECYCLOPENTANE ANNULATIONS OF ELECTRON
  196633. POOR ALKENES
  196634. 1994 X
  196635. 14274
  196636. ERIKSSON, M.
  196637. SynlettC
  196638. ORGANOCOPPER IODOTRIMETHYLSILANE CLAISEN REARRANGEMENT GAMMA,DELTA
  196639. UNSATURATED ACIDS CONJUGATE ADDITION STEREOCHEMICAL CONTROL ORGANOCOPPER REAGENTS ALKYLATION HALIDES M
  196640. 15283N
  196641. 2/28/96
  196642. PREPARATION OF g,d
  196643. UNSATURATED ACIDS VIA CONJUGATE ADDITION OF RCu(LII)
  196644. TMSI to ALLYLIC A,b
  196645. UNSATURATED ESTERS FOLLOWED BY CLAISEN REARRANGEMENT
  196646. 1994 X
  196647. 14275
  196648. PALACIOS, F.
  196649. SynlettCYALLYLAMINES ALLENES WITTIG
  196650. HORNER REACTION ENAMINES DERIVATIVES REACTIVITY AMINES OXIDES M
  196651. 15284N
  196652. 2/28/96
  196653. AjAN EFFICIENT and GENERAL STRATEGY FOR THE SYNTHESIS OF SECONDARY E
  196654. ALLYLAMINES FROM PHOSPHORYLATED ALLENES
  196655. 1994 X
  196656. 14276
  196657. A    TAMAO, K.
  196658. Synlett
  196659.     (DICHLOROMETHYL)DIMETHYLCHLOROSILANE HYDROXYMETHYLIDENE DIRADICAL FORMYL RADICAL HYDRINDAN OXIDATIVE CLEAVAGE OF THE SI
  196660. C BOND STEREOCONTROLLED SYNTHESIS JUNCTION STEREOCHEMISTRY SILAFUNCTIONAL COMPOUNDS CHIRALITY TRANSMISSION CYCLIZATION PROCESS ORGANIC
  196661. SYNTHESIS 
  196662. 15285N
  196663. 2/28/96
  196664. (DICHLOROMETHYL)DIMETHYLSILYL GROUP AS A HYDROXYMETHYLIDENE DIRADICAL EQUIVALENT 
  196665.  RADICAL ANNULATION OF DIENOLS and ITS APPLICATION to THE STEREOSELECTIVE SYNTHESIS OF CIS
  196666. HYDRINDAN and TRANS
  196667. HYDRINDAN RING SYSTEMS
  196668. 1994 X
  196669. 14277
  196670. IRIE, R.
  196671. SynlettC
  196672. (SALEN)MANGANESE(III) COMPLEXES HYDROGEN PEROXIDE BIS(TRIMETHYLSILYL) PEROXIDE N
  196673. METHYLIMIDAZOLE 2,2
  196674. DIMETHYLCHROMENE CATALYTIC ASYMMETRIC EPOXIDATION CHIRAL (SALEN)MANGANESE(III) COMPLEXES UNFUNCTIONALIZED OLEFINS ALKENE EPOXIDATION PORPHYRINSM
  196675. 15286N
  196676. 2/28/96
  196677. AbENANTIOSELECTIVE EPOXIDATION OF CHROMENE DERIVATIVES USING HYDROGEN PEROXIDE AS A TERMINAL OXIDANT
  196678. 1994 X
  196679. 14278
  196680. BIRKETT, M. A.
  196681. SynlettCQBENZYNES AMINOBENZOTRIAZOLES N
  196682. IODOSUCCINIMIDE TRAPPING INTRAMOLECULAR EFFICIENT M
  196683. 15287N
  196684. 2/28/96
  196685. IODOSUCCINIMIDE 
  196686.  A SUPERIOR REAGENT FOR THE GENERATION OF BENZYNES FROM 1
  196687. AMINOBENZOTRIAZOLES
  196688. 1994X
  196689. 14279
  196690. KRAUS, G. A.
  196691. SynlettC/BRIDGEHEAD RADICAL ANNULATION SYNTHESIS COBALT M
  196692. 15288N
  196693. 2/28/96
  196694. AeBRIDGEHEAD INTERMEDIATES IN ORGANIC SYNTHESIS CONSTRUCTION OF THE TETRACYCLIC SKELETON OF LEUCOTHOL
  196695. 1994 X
  196696. 14280
  196697. PRAKASH, O.
  196698. SynlettC
  196699. HYPERVALENT IODINE IODOBENZENE DIACETATE [HYDROXY(TOSYLOXY)IODO]BENZENE HETEROCYCLIC COMPOUNDS ONE
  196700. POT SYNTHESIS ORGANIC
  196701. SYNTHESIS CONVENIENT SYNTHESIS ALPHA
  196702. HYDROXYLATION CARBONYL
  196703. COMPOUNDS FACILE SYNTHESES M
  196704. 15289N
  196705. 2/28/96
  196706. AFHYPERVALENT IODINE REAGENTS IN THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS
  196707. 1994X
  196708. 14281
  196709. CLAYDEN, J.
  196710. J.C.S. Perkin Trans. 1CKHORNER
  196711. WITTIG REACTION STEREOSELECTIVE SYNTHESIS REDUCTION ALKENES KETONES M
  196712. 15290N
  196713. 2/28/96
  196714. ADDITIONS OF LITHIATED b
  196715. HYDROXY ALKYLDIPHENYLPHOSPHINE OXIDES to ALDEHYDES, AND PALLADIUM(II)
  196716. CATALYSED ALLYLIC TRANSPOSITIONS OF BIS
  196717. ACETOXY ALKYLDIPHENYLPHOSPHINE OXIDES:  SYNTHESIS OF O
  196718. PROTECTED (E,E)
  196719.  and (E,Z)HEPTA
  196720. OL and OF ALKYLDIPHENYLPHOSPHINE OXIDES BEARING
  196721. 1994X    1529
  196722. 1539Z
  196723. 14282
  196724. A    THEIL, F.
  196725. J.C.S. Perkin Trans. 1C;ORGANIC
  196726. SYNTHESIS SOLVENTS ENZYMES RESOLUTION ACETATE ACID M
  196727. 15291N
  196728. 2/28/96
  196729. ArDOUBLE ENANTIOSELECTIVE TRANSESTERIFICATION OF RACEMIC CARBOXYLIC ESTERS and CYCLIC MESO
  196730. DIOLS BY LIPASE CATALYSIS
  196731. 1994X    1509
  196732. 1516Z
  196733. 14283
  196734. SHEN, Y. C.
  196735. J.C.S. Perkin Trans. 1C
  196736. WITTIG M
  196737. 15292N
  196738. 2/28/96
  196739. NOVEL CONVERSION OF E STEREOSELECTIVITY TO Z STEREOSELECTIVITY IN TRIFLUOROMETHYLATED A,b
  196740. UNSATURATED ESTERS and NITRILES BY WAY OF O
  196741. METHYLATION OF AN YLIDE ANION
  196742. 1994X    1473
  196743. 1475Z
  196744. 14284
  196745. ABUSHANAB, F. A.
  196746. J.C.S. Perkin Trans. 1C+KETENE DITHIOACETALS PYRIMIDINE
  196747. DERIVATIVESM
  196748. 15293N
  196749. 2/28/96
  196750. AbA,A
  196751. DIOXOKETENE DITHIOACETALS AS STARTING MATERIALS FOR THE SYNTHESIS OF POLYSUBSTITUTED PYRIDINES
  196752. 1994X    1449
  196753. 1452Z
  196754. 14285
  196755. TAKESHITA, H.
  196756. J.C.S. Perkin Trans. 1C-C
  196757. 60 BUCKMINSTERFULLERENE ADDUCT C60 BENZYNE M
  196758. 15294N
  196759. 2/28/96
  196760. AsHIGH
  196761. PRESSURE DIELS
  196762. ALDER REACTION OF [60]FULLERENE WITH SEVERAL TROPONES. CHARACTERIZATION OF THE 1:1
  196763. CYCLOADDUCTS
  196764. 1994 X    1433
  196765. 1437Z
  196766. 14286
  196767. CURRAN, D. P.
  196768. J.C.S. Perkin Trans. 1C
  196769. TRANSFER CYCLIZATION REACTIONS 1,5 ALLYLIC ABSTRACTION ATOM TRANSFER
  196770. REACTIONS ALPHA
  196771. IODO ESTERS RESTRICTED ROTATION RATE CONSTANTS BETA
  196772. LACTAMS RING
  196773. CLOSURE NITROGEN ETHERS M
  196774. 15295N
  196775. 2/28/96
  196776. A~RADICAL TRANSLOCATION REACTIONS ACROSS AMIDES. 1,5
  196777. HYDROGEN
  196778. TRANSFER REACTIONS OF O
  196779. IODOBENZAMIDES and N
  196780. IODOBENZYL) AMIDES
  196781. 1994X    1377
  196782. 1393Z
  196783. 14287
  196784. SANJAYAN, G. J.
  196785. Ind. J. Chem. Sect. BC
  196786. LACTAMS M
  196787. 15296N
  196788. 2/28/96
  196789. AAACID
  196790. AIDED REACTIONS OF 3
  196791. ACYLAMINO
  196792. LACTAMS 
  196793.  SOME OBSERVATIONS
  196794. 1994 X
  196795. 14288
  196796. CHOWDHURY, P. K.
  196797. Ind. J. Chem. Sect. BM
  196798. 15297N
  196799. 2/28/96
  196800. PREPARATION OF CHLORO
  196801. NITROCOMPOUNDS FROM OLEFINS BY IN SITU GENERATION OF NITROSYL CHLORIDE FROM CHLOROTRIMETHYLSILANE and SODIUM NITRITE
  196802. 1994X
  196803. 14289
  196804. AHMED, A. F. S.
  196805. Ind. J. Chem. Sect. BM
  196806. 15298N
  196807. 2/28/96
  196808. ANSYNTHESIS OF SOME URIDINE DERIVATIVES VIA FORMATION OF THE EPOXY INTERMEDIATES
  196809. 1994 X
  196810. 14290
  196811. BANERJI, A.
  196812. Ind. J. Chem. Sect. BM
  196813. 15299N
  196814. 2/28/96
  196815. A/NOVEL RING
  196816. OPENING REACTION OF CHROMANONE OXIME
  196817. 1994 X
  196818. 14291
  196819. DHAWAN, S. N.
  196820. Ind. J. Chem. Sect. BM
  196821. 15300N
  196822. 2/28/96
  196823. A{ON THE MECHANISM OF FORMATION OF PYRAZOLES FROM 1,3
  196824. DIKETONES and HYDRAZINES 
  196825.  ISOLATION OF HYDROXYPYRAZOLINE INTERMEDIATES
  196826. 1994X
  196827. 14292
  196828. CHAUHAN, P. M. S.
  196829. Ind. J. Chem. Sect. BM
  196830. 15301N
  196831. 2/28/96
  196832. SYNTHESIS OF 1,3
  196833. SUBSTITUTED INDOLES, 2,4,6
  196834. SUBSTITUTED
  196835. TRIAZINES and 4,5
  196836. SUBSTITUTED PYRAZOLES AS POSSIBLE ANTIFILARIAL AGENTS
  196837. 1994 X
  196838. 14293
  196839. ORJALES, A.
  196840. Ind. J. Chem. Sect. BC
  196841. SERUM M
  196842. 15302N
  196843. 2/28/96
  196844. SYNTHESIS AND HYPOLIPIDEMIC ACTIVITY OF NOVEL 4
  196845. BENZOPYRAN
  196846. PHENYLALKANOIC and 4
  196847. THIOXO
  196848. BENZOPYRAN
  196849. PHENYLALKANOIC ACIDS and ESTERS
  196850. 1994X
  196851. 14294
  196852. Rao, C. C.B
  196853. Ind. J. Chem. Sect. BC
  196854. ACID M
  196855. 15303N
  196856. 2/28/96
  196857. AXA NEW METHODOLOGY FOR THE SYNTHESIS OF N
  196858. ACYLAMINOCINNAMATES and AMIDES FROM AZaLACTONES
  196859. 1994 X
  196860. 14295
  196861. BALU, N.
  196862. J.C.S. Chem. Commun.C
  196863. CYCLIZATION DERIVATIVES M
  196864. 15304N
  196865. 2/28/96
  196866. AeSYNTHESIS OF SUBSTITUTED DIOXABICYCLO[N.2.1]ALKANES THROUGH PALLADIUM CATALYSED OXIDATIVE CYCLISATION
  196867. 1994 X
  196868. 14296
  196869. BARAMEE, A.
  196870. J.C.S. Chem. Commun.M
  196871. 15305N
  196872. 2/28/96
  196873. A9FLASH VACUUM PYROLYSIS OF CYCLOPROPENE ANTHRACENE ADDUCTS
  196874. 1994X
  196875. 14297
  196876. UNDHEIM, K.
  196877. J.C.S. Chem. Commun.CTTRANSLOCATION OF RADICAL, ARYL, ALPHA AMINO RADICAL FORMATION AND CONJUGATE ADDITION
  196878. 15306N
  196879. 2/28/96
  196880. ALKYLATION OF AMINES VIA A 1,5
  196881. HYDROGEN SHIFT
  196882. 1994 X
  196883. 14298
  196884. DENICOLA, A.
  196885. J.C.S. Chem. Commun.C
  196886. PIPECOLIC ACID M
  196887. 15307N
  196888. 2/28/96
  196889. ApINTRAMOLECULAR ALKYLATION OF CARBOXYLIC ACIDS 
  196890.  APPLICATION to THE SYNTHESIS OF BOC
  196891. PROTECTED CYCLIC AMINO ACIDS
  196892. 1994 X
  196893. 14299
  196894. BARLUENGA, J.
  196895. J.C.S. Chem. Commun.CuDIELS
  196896. ALDER REACTIONS C=C
  196897. CONJUGATED CARBODIIMIDES 2
  196898. AZA 1,3
  196899. DIENES CYCLO
  196900. ADDITIONS CYCLOADDITION AZADIENES REAGENTS M
  196901. 15308N
  196902. 2/28/96
  196903. AGA NEW DOMINO SYNTHESIS OF POLYFUNCTIONALIZED PENTASUBSTITUTED PYRIDINES
  196904. 1994X
  196905. 14300
  196906. REDDY, N. P.
  196907. J.C.S. Chem. Commun.C@AROMATIC NITRO
  196908. COMPOUNDS RUTHENIUM CARBONYL NITROBENZENE AMINES M
  196909. 15309N
  196910. 2/28/96
  196911. A|PALLADIUM COMPLEX POTASSIUM CARBONATE
  196912. CATALYSED REDUCTIVE CARBONYLATION OF MONO
  196913. NITROAROMATIC and DI
  196914. NITROAROMATIC COMPOUNDS
  196915. 1994 X
  196916. 14301
  196917. BORNER, R. C.
  196918. J.C.S. Chem. Commun.M
  196919. 15310N
  196920. 2/28/96
  196921. AxA FLEXIBLE and RATIONAL SYNTHESIS OF SUBSTITUTED TRIPHENYLENES BY PALLADIUM
  196922. CATALYSED CROSS
  196923. COUPLING OF ARYLZINC HALIDES
  196924. 1994 X
  196925. 14302
  196926. BARLUENGA, J.
  196927. J.C.S. Chem. Commun.C
  196928. AMINO
  196929. BUTADIENES M
  196930. 15311N
  196931. 2/28/96
  196932. AmFirST [4+2] CYCLOADDITION REACTION BETWEEN VINYL FISCHER TYPE CARBENE COMPLEXES and CHIRAL 2
  196933. AMINO
  196934. DIENES
  196935. 1994X
  196936. 14303
  196937. AITKEN, R. A.
  196938. J.C.S. Chem. Commun.C
  196939. REACTIVITY M
  196940. 15312N
  196941. 2/28/96
  196942. FLASH VACUUM PYROLYSIS OF ALKOXYCARBONYL/SULFINYL STABILISED PHOSPHORUS YLIDES 
  196943.  GENERATION and INTRAMOLECULAR INSERTION OF ALKOXYCARBONYL(SULFENYL)CARBENES
  196944. 1994 X
  196945. 14304
  196946. KIDO, F.
  196947. J.C.S. Chem. Commun.C.EFFICIENT LACTONES VALEROLACTONES ROUTE GAMMA M
  196948. 15313N
  196949. 2/28/96
  196950. STERIC CONTROL BASED ON ALKYL SUBSTITUENTS IN THE [2,3] SIGMATROPIC REARRANGEMENT OF 9
  196951. MEMBERED ALLYLSULFONIUM YLIDES 
  196952.  A NEW ENTRY to THE STEREOSELECTIVE SYNTHESIS OF ELEMANE
  196953. TYPE SESQUITERPENOIDS
  196954. 1994X
  196955. 14305
  196956. MENDENHALL, G. D.
  196957. JACSK
  196958. (VOL 116, PG 1718,1994)M
  196959. 15314N
  196960. 2/28/96
  196961. ENDO CLOSURE OF THE 2
  196962. FORMYLBENZOYL RADICAL 
  196963. 1994X
  196964. 14306
  196965. Kim, S.B
  196966. JACSCe RADICAL ADDITION AZIDE HETEROCYCLE EXTRUSION NITROGEN CYCLIZATION ADDITION HYDRAZONE AZIRIDINE NOVELM
  196967. 15315N
  196968. 2/28/96
  196969. AINOVEL RADICAL CYCLIZATIONS OF ALKYL AZIDES. A NEW ROUTE to N
  196970. HETEROCYCLES
  196971. 1994 X    5521
  196972. 5522Y
  196973. 14307
  196974. BUSZEK, K. R.
  196975. JACSM
  196976. 15316N
  196977. 2/28/96
  196978. A%TOTAL SYNTHESIS OF OCTALACTIN A and B
  196979. 1994X    5511
  196980. 5512Y
  196981. 14308
  196982. JAMISON, T. F.
  196983. JACSC
  196984. JAMISON TFM
  196985. 15317N
  196986. 2/28/96
  196987. A5COBALT
  196988. MEDIATED TOTAL SYNTHESIS OF (+)
  196989. EPOXYDICTYMENE
  196990. 1994X    5505
  196991. 5506Y
  196992. 14309
  196993. CHEN, H. Y.
  196994. JACSM
  196995. 15318N
  196996. 2/28/96
  196997. AZDEAROMATIZATION OF FURAN:  STRUCTURE OF AN h2
  196998. FURAN COMPLEX and A SURVEY OF ITS REACTIVITY
  196999. 1994 X    5499
  197000. 5500Y
  197001. 14310
  197002. BILLERA, C. F.
  197003. LITTLE 
  197004. JACSCdDIRADICAL TRIMETHYLENEMETHANE INTRAMOLECULAR HYDROGEN ABSTRACTION TRANSFER CYANO NITRILE CYCLIZATIONM
  197005. 15319N
  197006. 2/28/96
  197007. AxHYDROGEN ATOM TRANSFER REACTIONS to TRIMETHYLENEMETHANE DIYLS. A NEW REACTIVITY PATTERN LEADING TO BICYCLIC RING SYSTEMS
  197008. 1994X    5487
  197009. 5488Y
  197010. 14311
  197011. WARNER, B. P.
  197012. JACSM
  197013. 15320N
  197014. 2/28/96
  197015. AESYNTHESIS and X
  197016. RAY STRUCTURE OF A ZIRCONOCENE COMPLEX OF TWO ALKYNES
  197017. 1994X    5471
  197018. 5472Y
  197019. 14312
  197020. Ito, H.B
  197021. JACSM
  197022. 15321N
  197023. 2/28/96
  197024. ZIRCONIUM
  197025. MEDIATED, HIGHLY DIASTEREOSELECTIVE RING CONTRACTION OF VINYLMORPHOLINE DERIVATIVES FROM A
  197026. AMINO ACIDS:  AN APPLICATION to THE SYNTHESIS OF (
  197027. MACRONECINE
  197028. 1994X    5469
  197029. 5470Y
  197030. 14313
  197031. TANKO, J. M.
  197032. JACSC
  197033. ABSOLUTE RATE CONSTANTS MULTIPLE SUBSTITUTIONS CHAIN CHLORINATIONS ATOM DISPROPORTIONATION STEREOCHEMISTRY ABSTRACTION COMBINATION INVERSION BROMINEM
  197034. 15322N
  197035. 2/28/96
  197036. SOLVENT PRESSURE EFFECTS IN FREE RADICAL REACTIONS .2. RECONCILIATION OF THE GAS and CONDENSED PHASE CHLORINATION OF CYCLOPROPANE
  197037. 1994 X    5162
  197038. 5166Y
  197039. 14314
  197040. VANDERSCHAAF, P. A.
  197041. JACSC
  197042. CYCLOPALLADATED COMPOUNDS (PI
  197043. ALLYL)PALLADIUM COMPLEXES TRANSITION
  197044. METALS ORGANIC
  197045. SYNTHESIS REACTIVITY MECHANISM REGIOSELECTIVITY CARBOPALLADATION ISOMERIZATION CHEMISTRY M
  197046. 15323N
  197047. 2/28/96
  197048. AXPALLADIUM
  197049. MEDIATED INTRAMOLECULAR C
  197050. N BOND FORMATION BETWEEN TERTIARY AMINES and ALKENES
  197051. 1994X    5134
  197052. 5144Y
  197053. 14315
  197054. KITA, Y.
  197055. JACSC
  197056. LACTAM ANTIBIOTICS DIRECTED ALDOL CONDENSATION ISOPENICILLIN
  197057. N SYNTHASE STEREOSELECTIVE SYNTHESIS BIOMIMETIC SYNTHESIS CHEMISTRY SULFOXIDES INTERMEDIATE DERIVATIVES PEPTIDES M
  197058. 15324N
  197059. 2/28/96
  197060. PUMMERER
  197061. TYPE CYCLIZATION OF ARNSTEIN TRIPEPTIDE ANALOGUES INDUCED BY O
  197062. SILYLATED KETENE ACETALS:  STUDIES OF PENICILLIN BIOSYNTHESIS
  197063. 1994X    5116
  197064. 5121Y
  197065. 14316
  197066. HUDLICKY, T.
  197067. ENZYMATIC ALDOL CONDENSATION PSEUDOMONAS
  197068. MENDOCINA KR1 ANTI
  197069. HIV AGENTS ABSOLUTE STEREOCHEMISTRY ORGANIC
  197070. SYNTHESIS D
  197071. GULONOLACTONE D
  197072. GLUCOSE ENANTIODIVERGENT SYNTHESIS ENANTIOSELECTIVE SYNTHESIS HYDROXYLATED PYRROLIDINES M
  197073. 15325N
  197074. 2/28/96
  197075. MICROBIAL OXIDATION OF AROMATICS IN ENANTIOCONTROLLED SYNTHESIS .2. RATIONAL DESIGN OF AZA SUGARS (ENDO
  197076. NITROGENOUS). TOTAL SYNTHESIS OF (+)
  197077. KIFUNENSINE, MANNOJIRIMYCIN, and OTHER GLYCOSIDASE INHIBITORS
  197078. 1994X    5099
  197079. 5107Y
  197080. 14317
  197081. FLORIO, S.
  197082. Gazz. Chim. Ital.
  197083. ELECTROPHILES METALS M
  197084. 15326N
  197085. 2/28/96
  197086. REGIOSELECTIVE CROSS
  197087. COUPLING REACTION OF PHENYLTHIOETHYNYL MAGNESIUM BROMIDE WITH ALLYLIC HALIDES 
  197088.  SYNTHESIS OF SKIPPED PHENYLTHIOPENTENYNES
  197089. 1994 X
  197090. 14318
  197091. DONATI, D.
  197092. Gazz. Chim. Ital.C
  197093. DERIVATIVESM
  197094. 15327N
  197095. 2/28/96
  197096. A*PHOTOCHEMICAL A
  197097. CYANOETHYLATION OF INDOLES
  197098. 1994X
  197099. 14319
  197100. ORIYAMA, T.
  197101. Bull. Chem. Soc. Jpn.
  197102. dCDSILYL ENOL ETHERS EFFICIENT ACETALS MILD REDUCTION CHLORIDE KETONES M
  197103. 15328N
  197104. 2/28/96
  197105. A ONE
  197106. STEP CONVERSION OF P
  197107. METHOXYBENZYL ETHERS INTO METHOXYMETHYL ETHERS BY THE ACTION OF DIMETHOXYMETHANE IN THE PRESENCE OF TIN(II) BROMIDE and BROMOMETHYL METHYL ETHER
  197108. 1994X
  197109. 14320
  197110. WATANABE, Y.
  197111. Bull. Chem. Soc. Jpn.C
  197112. CARBON
  197113. MONOXIDE HYDROSILANE M
  197114. 15329N
  197115. 2/28/96
  197116. ARCO2(CO)8
  197117. CATALYZED RING
  197118. OPENING CARBONYLATION OF CYCLIC ETHERS USING N
  197119. SILYLAMINES
  197120. 1994 X
  197121. 14321
  197122. NOMURA, E.
  197123. Bull. Chem. Soc. Jpn.CyFUNCTIONALIZED MACROCYCLES MOLECULAR INCLUSION 1
  197124. 1 CLATHRATE HOST
  197125. GUEST CRYSTAL CALIX<4>ARENE COMPLEXATION ABILITY ESTERSM
  197126. 15330N
  197127. 2/28/96
  197128. CALIXARENE
  197129. CATALYZED GENERATION OF DICHLOROCARBENE and ITS APPLICATION to ORGANIC REACTIONS 
  197130.  THE CATALYTIC ACTION OF OCTOPUS
  197131. TYPE CALIX[6]ARENE
  197132. 1994 X
  197133. 14322
  197134. HOPF, H.
  197135. Angew. Chem. Int. Ed. Engl. M
  197136. 15331N
  197137. 2/28/96
  197138. A.SYNTHESIS OF ENEDIYNES BY DIELS
  197139. ALDER ADDITION
  197140. 1994X    1099
  197141. 1100Y
  197142. 14323
  197143. TIETZE, L. F.
  197144. Angew. Chem. Int. Ed. Engl. M
  197145. 15332N
  197146. 2/28/96
  197147. AKREGIO
  197148.  and ENANTIOSELECTIVE SILANE
  197149. TERMINATED INTRAMOLECULAR HECK REACTIONS
  197150. 1994X    1089
  197151. 1091Y
  197152. 14324
  197153. DIEDRICH, M. K.
  197154. Angew. Chem. Int. Ed. Engl. M
  197155. 15333N
  197156. 2/28/96
  197157. THE PRESSURE EFFECT IN PERICYCLIC REARRANGEMENTS:  THE COPE REARRANGEMENT, ELECTROCYCLIZATION, and THE INTRAMOLECULAR DIELS
  197158. ALDER REACTION
  197159. 1994X    1079
  197160. 1081Y
  197161. 14325
  197162. RODRIGUEZ, J. G.
  197163. J.C.S. Perkin Trans. 2M
  197164. 15334N
  197165. 2/28/96
  197166. CYCLIZATION OF N
  197167. ACETYL
  197168. (ORTHO
  197169. CHLOROPHENYL)
  197170. AMINOBUT
  197171. ENENITRILE WITH ZEROVALENT NICKEL COMPLEXES 
  197172.  CONFORMATIONAL ANALYSIS OF THE N
  197173. CYANOPROP
  197174. ENYL CHAIN
  197175. 1994X    1393
  197176. 1396Z
  197177. 14326
  197178. QUAYLE, P.
  197179. Tet. Lett.CfCATALYZED RECONSTITUTIVE CONDENSATION CARBENE COMPLEXES VINYLIDENE TUNGSTEN CHROMIUM ALCOHOLS ALKYNES K|A TRANSITION METAL MEDIATED ACETYLENE
  197180. VINYLIDENE REARRANGEMENT HAS BEEN DEVELOPED FOR THE SYNTHESIS OF SPIROCYCLIC LACTONES.M
  197181. 15335N
  197182. 2/28/96
  197183. APTRANSITION METAL PROMOTED ACETYLENE ISOMERISATION REACTIONS IN ORGANIC SYNTHESIS
  197184. 1994 X    3801
  197185. 3804Y
  197186. 14327
  197187. ZHAO, Y. K.
  197188. Tet. Lett.C    ALCOHOLS K~THE STEREOSELECTIVE TRANSMETALLATION AND SUBSEQUENT ALKYLATION OF FUNCTIONALISED 1,1
  197189. (TRIBUTYLSTANNYL)ETHENES IS REPORTED.M
  197190. 15336N
  197191. 2/28/96
  197192. AITHE STEREOSELECTIVE FUNCTIONALISATION OF 1,1
  197193. (TRIBUTYLSTANNYL)ETHENES
  197194. 1994 X    3797
  197195. 3800Y
  197196. 14328
  197197. CARRENO, M. C.
  197198. Tet. Lett.C3REGIOSPECIFIC SYNTHESIS ANTHRACYCLINONES EFFICIENT 
  197199. RING SELECTIVITY OF DIELS
  197200. ALDER REACTIONS OF NAPHTHAZARIN THIODERIVATIVES WITH CYCLOPENTADIENE IS CONTROLLED BY CHOOSING THE ADEQUATE SULFUR SUBSTITUENT:  P
  197201. TOLYLSULFENYL AND P
  197202. TOLYLSULFINYL (UNDER BF3.OET(2) CATALYSIS) DERIVATIVES GIVE CYCLOADDITION ONLY ON THE C
  197203. 6 SUBSTITUTED TAUTOMER. THE OPPOSITE RING SELECTIVITY (EXCLUSIVE REACTION ON THE C
  197204. 2 SUBSTITUTED TAUTOMER) IS ACHIEVED IN THE REACTION OF THE P
  197205. TOLYLSULFONYL DERIVATIVE AT 
  197206. 78 DEGREES C.
  197207. 15337N
  197208. 2/28/96
  197209. AfCONTROL OF THE RING SELECTIVITY IN DIELS
  197210. ALDER REACTIONS OF NAPHTHAZARINS MEDIATED BY SULFUR FUNCTIONS
  197211. 1994X    3789
  197212. 3792Y
  197213. 14329
  197214. ARMESTO, D.
  197215. Tet. Lett.C"STABLE DERIVATIVES PHOTOCHEMISTRY 
  197216. ALTHOUGH PREVIOUS STUDIES HAVE SHOWN THAT OCYCLIC BETA,GAMMA
  197217. UNSATURATED OXIMES AND OXIME ETHERS DO NOT UNDERGO THE AZA
  197218. METHANE (ADPM) REARRANGEMENT, THE 2
  197219. METHYL
  197220. DIPHENYL
  197221. VINYLBUT
  197222. ENAL OXINE 5A, ITS METHYL ETHER 5B AND THE 2,2,4,4
  197223. TETRAPHENYLBUT
  197224. ENAL OXIME 14 GIVE THE CORRESPONDING CYCLOPROPYL DERIVATIVES 8A. 8B AND 15 BY THE ADPM PATH, IN A REACTION THAT IS CONTROLLED BY THE STABILITY OF THE INTERMEDIATE 1,3
  197225. BIRADICAL.
  197226. 15338N
  197227. 2/28/96
  197228. A<THE AZA
  197229. METHANE REARRANGEMENT OF b,g
  197230. UNSATURATED OXIMES
  197231. 1994 
  197232. nX    3785
  197233. 3788Y
  197234. 14330
  197235. ROBERTSON, J.
  197236. Tet. Lett.CFENOL ETHERS KETONES CYCLIZATIONS ACYLSILANES EPOXIDES REAGENT SILICON 
  197237. THE THIYL
  197238. RADICAL INDUCED FRAGMENTATION OF ALKENYL EPOXY SILANES HAS BEEN FOUND TO AFFORD ALPHA
  197239. TRIMETHYLSILYL ALDEHYDES AS THE IMMEDIATE PRODUCTS. THESE MAY BE ISOLATED, REARRANGED TO TRIMETHYLSILYL DIENOL ETHERS, OR CONVERTED TO 1,3
  197240. DIENES WITH HIGH STEREOSELECTIVITY.
  197241. 15339N
  197242. 2/28/96
  197243. A\FREE RADICAL REARRANGEMENT OF ALKENYL EPOXY SILANES. ISOLATION OF A
  197244. TRIMETHYLSILYL ALDEHYDES
  197245. 1994X    3777
  197246. 3780Y
  197247. 14331
  197248. STEVENS, C. V.
  197249. Tet. Lett.
  197250. kTHE CONSTRUCTION OF A CYCLOALKYL RING AT THE ALPHA
  197251. POSITION OF ALDEHYDES BY CYCLIZATION OF OMEGA
  197252. HALOALDIMINES IS DESCRIBED. ALKYLATION OF THE CORRESPONDING ALDIMINES WITH ALPHA,OMEGA
  197253. DIHALOALKANES FOLLOWED BY TREATMENT WITH LDA RESULTS IN A CONVENIENT ACCESS TO ALPHA,ALPHA
  197254. CYCLOBISALKYLATED ALDIMINES WHICH ARE HYDROLYZED TO THE ALPHA,ALPHA
  197255. CYCLOALKYLALDEHYDES.
  197256. 15340N
  197257. 2/28/96
  197258. A7A,A
  197259. CYCLOBISALKYLATION OF ALDEHYDES VIA w
  197260. HALOALDIMINES
  197261. 1994 X    3763
  197262. 3766Y
  197263. 14332
  197264. MINISCI, F.
  197265. Tet. Lett.C
  197266. HETEROAROMATIC BASES 
  197267. NEW FREE
  197268. RADICAL SYNTHESES WERE DEVELOPED UNDER GIF
  197269. BARTAN CONDITIONS BY TRAPPING T
  197270. RADICALS WITH ELECTRON
  197271. RICH ALKENES (VINYL ETHER, STYRENE, ALPHA
  197272. METHYLSTYRENE) AND ACETALDEHYDE.M
  197273. 15341N
  197274. 2/28/96
  197275. A@NEW FREE
  197276. RADICAL SYNTHESES UNDER GIF
  197277. BARTON OXIDATION CONDITIONS
  197278. 1994 X    3759
  197279. 3762Y
  197280. 14333
  197281. NANGIA, A.
  197282. Tet. Lett.K
  197283. THE CYCLOPENTAPYRANONES (
  197284. 7 AND (
  197285. 13, REPRESENTING THE CIS
  197286. FUSED 9
  197287. CARBON CORE OF IRIDOID LACTONES, ARE SYNTHESISED FROM (+)
  197288. PULEGONE.M
  197289. 15342N
  197290. 2/28/96
  197291. INTRAMOLECULAR HORNER
  197292. WADSWORTH
  197293. EMMONS REACTION IN BASE SENSITIVE SUBSTRATES:  ENANTIOSPECIFIC SYNTHESIS OF IRIDOID MONOTERPENE LACTONES
  197294. 1994X    3755
  197295. 3758Y
  197296. 14334
  197297. Kim, G. C.B
  197298. Tet. Lett.C
  197299. REARRANGEMENT ROUTE K
  197300. INTRAMOLECULAR DIAZOKETOESTER
  197301. THIOLMIDE ANNULATION REACTION IN THE PRESENCE OF RHODIUM(LL) ACETATE DIMER PROVIDED A NEW WAY TO PYRROLIZIDINE SKELETONES. (+/
  197302. SURPINIDINE WAS SYNTHESIZED BY SUBSEQUENT MANIPULATIONS.M
  197303. 15343N
  197304. 2/28/96
  197305. AZA SYNTHESIS OF (+/
  197306. SUPINIDINE VIA AN INTRAMOLECULAR CARBENOID
  197307. THIOMIDE COUPLING REACTION
  197308. 1994 X    3747
  197309. 3748Y
  197310. 14335
  197311. Son, Y. C.B
  197312. Tet. Lett.C
  197313. ACIDS 
  197314. 0AN EFFICIENT AND ENANTIOSELECTIVE METHOD FOR THE PREPARATION OF A CHIRAL PRIMARY AMINE HAS BEEN DEVELOPED. STARTING FROM N
  197315. PROTECTED L OR D
  197316. AMINO ACID THE SEQUENCE INVOLVES COUPLING WITH N
  197317. METHOXY
  197318. METHOXY
  197319. METHYLAMINE, ACYLATION, OLEFINATION WITH POTASSIUM BIS(TRIMETHYLSILYL)AMIDE, AND HYDROGENATION.
  197320. 15344N
  197321. 2/28/96
  197322. AEAN EFFICIENT and ENANTIOSELECTIVE SYNTHESIS OF A CHIRAL PRIMARY AMINE
  197323. 1994 X    3745
  197324. 3746Y
  197325. 14336
  197326. SHINOKUBO, H.
  197327. Tet. Lett.C)RING ENLARGEMENT REACTION SILANES ESTERS 
  197328. AN ADDITION OF BENZALDEHYDE TO AN ETHEREAL SOLUTION OF TERT
  197329. BUTYLDIMETHYLSILYLDIBROMO
  197330.  METHYLLITHIUM PROVIDED ALPHA
  197331. BROMO
  197332. ALPHA
  197333. SILYL KETONE. FURTHER TREATMENT OF THE ALPHA
  197334. BROMO
  197335. ALPHA
  197336. SILYL KETONE WITH BUTYLLITHIUM AFFORDED ENOLATE WHICH PROVIDED BETA
  197337. HYDROXY
  197338. ALPHA
  197339. SILYL KETONE UPON TREATMENT WITH ALDEHYDE IN ETHER. THE ENOLATE GAVE ALPHA,BETA
  197340. UNSATURATED KETONE OR MONOSILYL ETHER OF 2
  197341. DIOL IN THF INSTEAD OF ETHER.
  197342. 15345N
  197343. 2/28/96
  197344. AsONE
  197345. POT SYNTHESIS OF A,b
  197346. UNSATURATED KETONES FROM TERT
  197347. BUTYLDIMETHYLSILYLDIBROMOMETHANE and TWO DIFFERENT ALDEHYDES
  197348. 1994X    3741
  197349. 3744Y
  197350. 14337
  197351. NAKANISHI, S.
  197352. Tet. Lett.C
  197353. IRON TRICARBONYL COMPLEXES K
  197354. ACYL HALIDES ADJACENT TO (ETA(4)
  197355. DIENE)FE(CO)(3) GROUP REACT WITH ALLYLTRIMETHYLSILANES WITHOUT CATALYST TO GIVE THE CORRESPONDING ALLYL KETONES IN HIGH YIELDS.M
  197356. 15346N
  197357. 2/28/96
  197358. ASALLYLATION OF ACYL HALIDES ADJACENT to (h4
  197359. DIENE)FE(CO)3 FRAGMENT WITH ALLYLSILANES
  197360. 1994X    3727
  197361. 3728Y
  197362. 14338
  197363. A    MAYON, P.
  197364. Tet. Lett.
  197365. wCCALCOHOLS HYDROXYMETHYLATION STEREOCHEMISTRY PRODUCT SILICON ETHERS 
  197366. THE CYCLIZATION OF 2
  197367. HEXEN
  197368. YL RADICALS IN CONFORMATIONALY BIASED SUGAR RING SYSTEMS DEPENDS ON THE STEREOCHEMISTRY OF THE STARTING ALLYLIC ALCOHOL AND PROCEEDS EXCLUSIVELY VIA THE 6
  197369. ENDO MODE WITH A PREFERENCE FOR THE FORMATION OF CIS FUSED
  197370. RINGS.
  197371. 15347N
  197372. 2/28/96
  197373. AgEXCLUSIVE 6
  197374. ENDO RADICAL CYCLIZATIONS OF A
  197375. SILYL RADICALS DERIVED FROM CARBOHYDRATE ALLYLIC SILYLETHERS
  197376. 1994X    3703
  197377. 3706Y
  197378. 14339
  197379. BERNARDHENRIET, C. D.
  197380. Tet. Lett.CrOXIME ETHERS INTRAMOLECULAR ADDITION STEREO
  197381. SELECTIVITY REGIO
  197382. SELECTIVITY SYNTHETIC ROUTE GENERATION CARBON RINGS 
  197383. ALLENIC HYDRAZONES UNDERGO HYDROSTANNYLATION TO AFFORD CYCLOPENTENE DERIVATIVES AND LINEAR REARRANGED PRODUCTS DEPENDING ON THE SUBSTITUTION OF THE ALLENIC AND HYDRAZONE MOIETIES. A FIRST EXAMPLE OF ASYMMETRIC RADICAL CYCLIZATION OF A SAMP BETA
  197384. ALLENIC HYDRAZONE IS DESCRIBED.
  197385. 15348N
  197386. 2/28/96
  197387. ACRADICAL CYCLIZATION OF b
  197388. ALLENIC HYDRAZONES. AN ASYMMETRIC APPROACH
  197389. 1994 X    3699
  197390. 3702Y
  197391. 14340
  197392. A    SPINO, C.
  197393. Tet. Lett.
  197394. .AN OPTICALLY PURE ADVANCED INTERMEDIATE TO THE QUASSINOIDS WAS PREPARED VIA THE DIENE
  197395. TRANSMISSIVE DIELS
  197396. ALDER CYCLOADDITION STRATEGY. THE ABSOLUTE STEREOCHEMISTRY OF THE INTRAMOLECULAR CYCLOADDITION WAS CONTROLLED BY A METHYL AND A T
  197397. BUTYLDIMETHYLSILYLOXY GROUP VIA A CHAIR
  197398. LIKE ENDO TRANSITION STATE.
  197399. 15349N
  197400. 2/28/96
  197401. AEENANTIOSELECTIVE SYNTHESIS OF AN ADVANCED INTERMEDIATE to QUASSINOIDS
  197402. 1994 X    3683
  197403. 3686Y
  197404. 14341
  197405. zA    Wu, X. M.B
  197406. Tet. Lett.K
  197407. FUNCTIONALIZED THIOPHENES WERE READILY PREPARED BY REACTING ELECTROPHILES WITH 3
  197408. LITHIOTHIOPHENE AT ROOM TEMPERATURE. 3
  197409. LITHIOTHIOPHENE WAS FOUND TO BE STABLE IN HEXANE AT ROOM TEMPERATURE.M
  197410. 15350N
  197411. 2/28/96
  197412. AYROOM TEMPERATURE STABLE 3
  197413. LITHIOTHIOPHENE:  A FACILE SYNTHESIS OF 3
  197414. FUNCTIONAL THIOPHENES
  197415. 1994 X    3673
  197416. 3674Y
  197417. 14342
  197418. A    SOBTI, A.
  197419. Tet. Lett.C
  197420. GLYCOSIDES ALCOHOLS K
  197421. THE C
  197422. HYDROXYL GROUP OF L
  197423. RHAMNAL (4) AND D
  197424. GLUCAL 7 UNDERWENT S(N)2'
  197425. SELECTIVE MITSUNOBU DISPLACEMENTS WITH SUBSTITUTED PHENOXIDE NUCLEOPHILES. THESE REACTIONS PROVIDE ACCESS TO THE CORRESPONDING ALPHA
  197426. ARYLGLYCOSIDE.M
  197427. 15351N
  197428. 2/28/96
  197429. AMMITSUNOBU REACTIONS OF GLYCALS WITH PHENOXIDE NUCLEOPHILES ARE SN2'
  197430. SELECTIVE
  197431. 1994 X    3661
  197432. 3664Y
  197433. 14343
  197434. MAJEWSKI, M.
  197435. Tet. Lett.C@LITHIUM AMIDE BASES ASYMMETRIC
  197436. SYNTHESIS CLEAVAGE ENOLATE ROUTE 
  197437. CSYNTHESIS OF TROPANE ALKALOIDS DARLINGINE, CHALCOSTROBAMINE AND ISOBELLENDINE BOTH IN THE RACEMIC FORM AND AS UNNATURAL ENANTIOMERS IS DESCRIBED. ENANTIOSELECTIVE DEPROTONATION OF TROPINONE, WHICH PROCEEDED WITH CA 90% EE, WAS THE KEY STEP IN EACH OF THE SYNTHESES. ENANTIOSELECTIVITY WAS INCREASED IN THE PRESENCE OF LICL.
  197438. 15352N
  197439. 2/28/96
  197440. AGSYNTHESIS Of PYRANOTROPANES VIA ENANTIOSELECTIVE DEPROTONATION STRATEGY
  197441. 1994X    3653
  197442. 3656Y
  197443. 14344
  197444. DANIELI, B.
  197445. TetrahedronC
  197446. BIOGENETIC
  197447. TYPE SYNTHESIS INDOLE ALKALOIDS STEREOSPECIFIC MODELS VINCA ALKALOIDS REGIO
  197448. MODELS BIOSYNTHESIS TABERSONINE VINCADIFFORMINE VINDOLINE 
  197449. OXOVINCADIFFORMINE ETHYL ESTER 14 HAS BEEN SYNTHESIZED THROUGH AN INTRAMOLECULAR [4 PI+2 PI] CYCLOADDITION OF THE 3
  197450. OXOSECODINE 13 FIRST PREPARED IN TURN FROM THE ENAMIDE 10 BY DEHYDROGENATION WITH BENZENESELENINIC ANHYDRIDE. AN INSIGHT INTO THE CONVERSION OF 10 INTO 13 WAS GAINED, RESULTING IN THE SUGGESTION OF A PLAUSIBLE MECHANISTIC PATHWAY.
  197451. 15353N
  197452. 2/28/96
  197453. AuASPIDOSPERMA ALKALOIDS VIA CYCLIZATION OF SECODINE INTERMEDIATE:  SYNTHESIS OF (+/
  197454. OXOVINCADIFFORMINE ETHYL ESTER
  197455. 1994X    6941
  197456. 6954Y
  197457. 14345
  197458. MCNELIS, B. J.
  197459. TetrahedronC&STEREOCHEMICAL CONTROL QUINONES DIENE 
  197460. THE INTRAMOLECULAR DIELS
  197461. ALDER REACTIONS (IMDA) OF A SERIES OF 2
  197462. SULFONE SUBSTITUTED 1
  197463. FURYL
  197464. PENTEN
  197465. OLS, 5A
  197466. C, HAVE BEEN STUDIED. AS THE STERIC DEMANDS OF THE ALKYL GROUP ON THE SULFONE WAS INCREASED THE RATE AND PRODUCT YIELDS IN THE IMDA REACTION HAVE ALSO BEEN OBSERVED TO INCREASE. THE KINETICS OF THESE SYSTEMS HAVE BEEN STUDIED IN DETAIL AS WELL AS SOLVENT EFFECTS TO QUANTIFY SUBSTITUENT GROUP EFFECTS IN THE CYCLIZATION REACTIONS. ACTIVATED DIENOPHILES (CO(2)ME) IN THESE SYSTEMS HAB7VE BEEN SHOWN TO BE VERY REACTIVE, CYCLIZING AT AMBIENT
  197467. 15354N
  197468. 2/28/96
  197469. AeSYNTHETIC and KINETIC STUDIES OF SUBSTITUENT EFFECTS IN THE FURAN INTRAMOLECULAR DIELS
  197470. ALDER REACTION
  197471. 1994X    6767
  197472. 6782Y
  197473. 14346
  197474. AUGUSTI, R.
  197475. TetrahedronCuCARBINOLAMINE TUMOR INHIBITORS ANTILEUKEMIC ACTIVITY ANTINEOPLASTIC ACTIVITY DERIVATIVES ANALOGS ALKALOIDS CHEMISTRY 
  197476. (THE SYNTHETIC USEFULNES OF A NEW METHOD OF 1,2,3,
  197477. TRIAZOLE SYNTHESIS HAS BEEN DEMONSTRATED. BY EMPLOYING CYCLIC ENAMINO ESTERS 3 AND ENAMINO KETONES 4 IN REACTIONS WITH 5,7
  197478. DINITRO
  197479. DIAZO
  197480. DIHYDRO
  197481. INDOL
  197482. ONE (1), BICYCLIC TRIAZOLES 5 AND 6 HAVE BEEN PREPARED IN GOOD TO EXCELLENT YIELDS.
  197483. 15355N
  197484. 2/28/96
  197485. A~BICYCLIC TRIAZOLES FROM A DIAZO TRANSFER REACTION BETWEEN CYCLIC ENAMINONES and 5,7
  197486. DINITRO
  197487. DIAZO
  197488. DIHYDRO
  197489. INDOL
  197490. 1994 X    6723
  197491. 6726Y
  197492. 14347
  197493. SCHINZER, D.
  197494. SynlettC
  197495. PROPARGYLIC SILANES ALLYLSILANES 
  197496.  ALLYL SILANE SILYL LEWIS ACID AMBERLYST ENONE CONJUGATE ADDITION INTRAMOLECULAR MAJETICH ALLENEM
  197497. 15356N
  197498. 2/28/96
  197499. AGAMBERLYST
  197500.  A VERSATILE CATALYST FOR SILICON
  197501. TERMINATED CYCLIZATIONS
  197502. 1994X
  197503. 14348
  197504. MIWA, K.
  197505. SynlettM
  197506. 15357N
  197507. 2/28/96
  197508. AxA NEW SYNTHESIS OF 5
  197509. TRIMETHYLSILYL
  197510. DIHYDROFURANS FROM b
  197511. TRIMETHYLSILOXYKETONES UTILIZING TRIMETHYLSILYLDIAZOMETHANE
  197512. 1994 X
  197513. 14349
  197514. HARIRI, M. A.
  197515. SynlettM
  197516. 15358N
  197517. 2/28/96
  197518. A~GENERATION and [4+2] CYCLOADDITIONS OF DIMETHYL
  197519. BIS(BROMOMETHYLENE) FURAN
  197520. DIOATE, A FURAN ANALOGUE OF O
  197521. QUINODIMETHANE
  197522. 1994 X
  197523. 14350
  197524. SANTOYOGONZALEZ, F.
  197525. SynlettC
  197526. DISACCHARIDES M
  197527. 15359N
  197528. 2/28/96
  197529. AXRADICAL b
  197530. ELIMINATION OF VICINAL PHENYLSELENIDE and XANTHATE AZIDES IN SUGAR DERIVATIVES
  197531. 1994 X
  197532. 14351
  197533. MONTEIRO, N.
  197534. SynlettM
  197535. 15360N
  197536. 2/28/96
  197537. PALLADIUM CARBENOIDS FROM ENOLATES OF A
  197538. SULFONYL e
  197539. ACETYLENIC ESTERS, NITRILES OR KETONES 
  197540.  EVIDENCE FOR THE EXISTENCE OF THESE INTERMEDIATES
  197541. 1994X
  197542. 14352
  197543. ISHIBASHI, H.
  197544. Synlett
  197545. C=ENANTIOSELECTIVE SYNTHESIS CARBAPENEM ANTIBIOTICS ROUTE PS
  197546. 15361N
  197547. 2/28/96
  197548. A_ASYMMETRIC INDUCTION IN RADICAL CYCLIZATION LEADING to b
  197549. LACTAMS 
  197550.  FORMAL SYNTHESIS OF (+)
  197551. 1994X
  197552. 14353
  197553. CSUZDI, E.
  197554. SynlettC
  197555. DERIVATIVES M
  197556. 15362N
  197557. 2/28/96
  197558. AgNEW FORMATION OF PYRROLIZINES BY INTRAMOLECULAR CYCLIZATION OF PHENACYL SUBSTITUTED TETRAHYDROPYRIDINES
  197559. 1994X
  197560. 14354
  197561. BRINGMANN, G.
  197562. SynlettM
  197563. 15363N
  197564. 2/28/96
  197565. NOVEL CONCEPTS IN DIRECTED BIARYL SYNTHESIS .42. A NEW APPROACH to ATROPOSELECTIVE BIARYL SYNTHESIS, UTILIZING CHIRAL CARBON
  197566. CARBON BRIDGES
  197567. 1994X
  197568. 14355
  197569. LANGER, F.
  197570. SynlettCMFUNCTIONALIZED SECONDARY ALCOHOLS ALDEHYDES REAGENTS CHLORIDES KETONES ALPHA M
  197571. 15364N
  197572. 2/28/96
  197573. ATPREPARATION OF NEW POLYFUNCTIONAL DIORGANOZINCS USING A BORON
  197574. ZINC EXCHANGE REACTION
  197575. 1994 X
  197576. 14356
  197577. A    HAYES, P.
  197578. SynlettC
  197579. DIELS
  197580. ALDER REACTIONS M
  197581. 15365N
  197582. 2/28/96
  197583. firST HETEROCYCLOADDITION OF IN SITU GENERATED 2
  197584. TOLYLSULFINYLACROLEIN 
  197585.  SIMPLE SYNTHESIS OF FUNCTIONALISED DIHYDROPYRAN and SPIROKETAL DERIVATIVES
  197586. 1994X
  197587. 14357
  197588. KNOLKER, H. J.
  197589. SynlettC<MEDIATED TOTAL SYNTHESIS IRON TRICARBONYL TETRACARBONYLIRON M
  197590. 15366N
  197591. 2/28/96
  197592. TRANSITION METAL
  197593. DIENE COMPLEXES IN ORGANIC SYNTHESIS .20. DEVELOPMENT OF HIGHLY EFFICIENT 1
  197594. BUTADIENE CATALYSTS FOR THE COMPLEXATION OF 1,3
  197595. DIENES BY THE TRICARBONYLIRON FRAGMENT
  197596. 1994 X
  197597. 14358
  197598. A    MONTI, H.
  197599. SynlettCiCATALYZED ENE REACTIONS CYCLOPENTANE ANNULATION TRIMETHYLSILYLCYCLOPENTANE ANNULATION CONJUGATE ADDITION M
  197600. 15367N
  197601. 2/28/96
  197602. At[2+2] VERSUS [3+2] CYCLOADDITION OF ALLYLSILANES 
  197603.  THE DRAMATIC EFFECT OF LEWIS ACID and ELECTRON
  197604. DEFICIENT PARTNERS
  197605. 1994 X
  197606. 14359
  197607. FANG, J. M.
  197608. SynlettC
  197609. SIALIC ACID PEPTIDE
  197610. BOND FORMATION N
  197611. ACETYLNEURAMINATE LYASE ONE
  197612. POT SYNTHESIS ENZYMATIC
  197613. SYNTHESIS TRANS
  197614. ESTERIFICATION ENOL ESTERS CARBOHYDRATE SYNTHESIS LIPASE CATALYSIS ACYL TRANSFER M
  197615. 15368N
  197616. 2/28/96
  197617. A[ENZYMES IN ORGANIC SYNTHESIS 
  197618.  ALTERATION OF REVERSIBLE REACTIONS to IRREVERSIBLE PROCESSES
  197619. 1994X
  197620. 14360
  197621. KING, J. A.
  197622. Syn. Commun.CmSUBSTITUTED PYRIDINES METHOXYCARBONYL GROUP IODIDE DEMETHYLATION ISOQUINOLINE BROMIDE AMINES RATES STATE AM1 M
  197623. 15369N
  197624. 2/28/96
  197625. AmTHE PREPARARTION OF N
  197626. METHYLATED PYRIDINIUM SALTS VIA THE DECARBOXYLATION OF N
  197627. CARBOMETHOXYPYRIDINIUM CATIONS
  197628. 1994X    1923
  197629. 1935Y
  197630. 14361
  197631. A    KOLAR, P.
  197632. Syn. Commun.C
  197633. ETHYL M
  197634. 15370N
  197635. 2/28/96
  197636. AIA CONVENIENT SYNTHESIS OF SUBSTITUTED PYRROLES FROM ESTERS OF AMINO ACIDS
  197637. 1994X    1887
  197638. 1893Y
  197639. 14362
  197640. JEDLOVSKA, E.
  197641. Syn. Commun.M
  197642. 15371N
  197643. 2/28/96
  197644. AAA SIMPLE ONE
  197645. POT PROCEDURE FOR THE SYNTHESIS OF 1,3,4
  197646. OXADIAZOLES
  197647. 1994X    1879
  197648. 1885Y
  197649. 14363
  197650. Kim, K. M.B
  197651. Syn. Commun.M
  197652. 15372N
  197653. 2/28/96
  197654. AFFACILE SYNTHESES OF 2
  197655. ALKYL
  197656. DIHYDRO
  197657. METHYLBENZOFURAN DERIVATIVES
  197658. 1994X    1859
  197659. 1870Y
  197660. 14364
  197661. DALLEMAGNE, P.
  197662. Syn. Commun.M
  197663. 15373N
  197664. 2/28/96
  197665. ATA CONVENIENT REARRANGEMENT OF 1
  197666. PHENYLPYRROLE
  197667. CARBOXALDEHYDES INTO THEIR 3
  197668. ISOMERS
  197669. 1994X    1855
  197670. 1857Y
  197671. 14365
  197672. RAJAKUMAR, P.
  197673. Syn. Commun.M
  197674. 15374N
  197675. 2/28/96
  197676. AMCYCLOADDITION APPROACH FOR THE SYNTHESIS OF SOME HINDERED N
  197677. BENZOYLIMIDAZOLES
  197678. 1994X    1847
  197679. 1853Y
  197680. 14366
  197681. HIRANO, M.
  197682. Syn. Commun.C
  197683. ORGANIC REACTIONS 
  197684. SILICA ACID M
  197685. 15375N
  197686. 2/28/96
  197687. A FACILE PREPARATION OF AN ALUMINA
  197688. SUPPORTED CHROMIUM REAGENT and ITS APPLICATION to THE CHEMOSELECTIVE OXIDATION OF VARIOUS ALCOHOLS
  197689. 1994X    1823
  197690. 1831Y
  197691. 14367
  197692. CAUBERE, C.
  197693. Syn. Commun.C
  197694. METHYL ETHERS CLEAVAGE M
  197695. 15376N
  197696. 2/28/96
  197697. AHSELECTIVE DEMETHYLATION and DEMETHOXY
  197698. THIOALKYLATION OF 5
  197699. METHOXYINDOLES
  197700. 1994X    1799
  197701. 1808Y
  197702. 14368
  197703. MOREAU, P.
  197704. Syn. Commun.M
  197705. 15377N
  197706. 2/28/96
  197707. ATA CONVENIENT SYNTHESIS OF DIVERSELY SUBSTITUTED N,N
  197708. DIMETHYL
  197709. ALKENAMIDES
  197710. 1994X    1781
  197711. 1787Y
  197712. 14369
  197713. DUTTON, J. K.
  197714. J.C.S. Chem. Commun.M
  197715. 15378N
  197716. 2/28/96
  197717. A9A TOTAL SYNTHESIS OF GELSEMINE 
  197718.  OXINDOLE SPIROANNELATION
  197719. 1994X
  197720. 14370
  197721. A    KONDO, T.
  197722. J.C.S. Chem. Commun.C
  197723. RECONSTITUTIVE CONDENSATION 
  197724. SELECTIVE SYNTHESES ACRYLIC COMPOUNDS ACID
  197725. DERIVATIVES 
  197726. ALLYLATION 
  197727. ACETYLENES 
  197728. ACETATES 
  197729. KETONES M
  197730. 15379N
  197731. 2/28/96
  197732. AgA NEW ROUTE to 2(5H)
  197733. FURANONES VIA RUTHENIUM
  197734. CATALYSED OXIDATIVE CYCLOCARBONYLATION OF ALLYLIC ALCOHOLS
  197735. 1994 X
  197736. 14371
  197737. PYNE, S. G.
  197738. J.C.S. Chem. Commun.C&SUBSTITUTION REAGENTS KETONES 
  197739. SULFUR M
  197740. 15380N
  197741. 2/28/96
  197742. AeDIASTEREOSELECTIVE CONJUGATE ADDITIONS REACTIONS OF A LITHIATED ALLYLIC SULFOXIMINE to ACYCLIC ENONES
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  197744. 14372
  197745. MADSEN, R.
  197746. J.C.S. Chem. Commun.C
  197747. GLYCOSIDES M
  197748. 15381N
  197749. 2/28/96
  197750. A-DIPENT
  197751. ENYL ACETALS AS ACETALIZATION AGENTS
  197752. 1994 X
  197753. 14373
  197754. WESTON, W. S.
  197755. J.C.S. Chem. Commun.C
  197756. CHELATE M
  197757. 15382N
  197758. 2/28/96
  197759. AHTHE DOUBLE CARBONYLATION OF DIIODOMETHANE CATALYSED BY RHODIUM COMPLEXES
  197760. 1994X
  197761. 14374
  197762. Cao, P.B
  197763. J.C.S. Chem. Commun.M
  197764. 15383N
  197765. 2/28/96
  197766. ACDIFLUOROIODOMETHANE 
  197767.  PRACTICAL SYNTHESIS and REACTION WITH ALKENES
  197768. 1994 X
  197769. 14375
  197770. CARDILLO, G.
  197771. J.C.S. Chem. Commun.C?ALDOL REACTION AMINO
  197772. ACIDS 
  197773. ADDITION 
  197774. DERIVATIVES 
  197775. KETONES M
  197776. 15384N
  197777. 2/28/96
  197778. CONJUGATE ADDITION OF CHLORIDE to A,b
  197779. UNSATURATED CHIRAL IMIDES PROMOTED BY BCL3
  197780. DERIVATIVES 
  197781.  A SYNTHESIS OF 3
  197782. CHLOROBUTANOIC ACID
  197783. 1994X
  197784. 14376
  197785. BARKS, J. M.
  197786. J.C.S. Chem. Commun.C(SYNTHETIC ROUTES CYCLIZATIONS 
  197787. ALCOHOLS M
  197788. 15385N
  197789. 2/28/96
  197790. AiA STEREOSELECTIVE APPROACH to ANNULATED TETRAHYDROFURANS BY IODOCYCLISATIONS OF 2
  197791. ALKENYLCYCLOALKAN
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  197793. 14377
  197794. BARTOLI, G.
  197795. J.C.S. Chem. Commun.C8CARBONYL COMPOUNDS CONVENIENT SYNTHESIS CHELATION ALPHA M
  197796. 15386N
  197797. 2/28/96
  197798. HIGHLY STEREOSELECTIVE SYNTHESIS OF A,b
  197799. UNSATURATED KETONES BY CECL3 MEDIATED ADDITION OF GRIGNARD REAGENTS to b
  197800. ENAMINO KETONES
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  197802. 14378
  197803. BHATIA, B.
  197804. J.C.S. Chem. Commun.CcLEWIS
  197805. ACID CATALYSTS HOMOGENEOUS CATALYSIS MICHAEL REACTIONS
  197806. ALDOL REACTION CONDENSATION 
  197807. CHLORIDE M
  197808. 15387N
  197809. 2/28/96
  197810. COBALT
  197811. CATALYSED 3
  197812. COMPONENT COUPLING INVOLVING KETONES OR KETOESTERS, ALDEHYDES and ACETONITRILE 
  197813.  A NOVEL ONE
  197814. POT SYNTHESIS OF b
  197815. ACETAMIDO KETONES
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  197817. 14379
  197818. Yeh, M. C. P.B
  197819. J.C.S. Chem. Commun.C
  197820. COMPLEXES 
  197821. REAGENTS 
  197822. SYSTEMS M
  197823. 15388N
  197824. 2/28/96
  197825. CONSTRUCTION OF FUSED BICYCLO
  197826. [5.3.0]DECANE and BICYCLO
  197827. [5.4.0]UNDECANE RING SKELETONS VIA SEQUENTIAL ADDITIONS OF NUCLEOPHILES to TRICARBONYLTROPYLIUMCHROMIUM TETRAFLUROBORATE
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  197829. 14380
  197830. KITA, Y.
  197831. J.C.S. Chem. Commun.
  197832. HYDROXY AROMATIC COMPOUNDS DIHYDROXYSTYRENE DERIVATIVES 
  197833. HOMOPHTHALIC ANHYDRIDES SKELETAL TYPE CYCLOADDITION SYSTEM (+/
  197834. FREDERICAMYCIN
  197835. 15389N
  197836. 2/28/96
  197837. OXIDATIVE INTRAMOLECULAR [4+2] CYCLOADDITION OF SILYLENE
  197838. PROTECTED 2
  197839. PYRIDONE DERIVATIVES 
  197840.  A SHORT and EFFICIENT SYNTHESIS OF THE DEF
  197841. RING OF FREDERICAMYCIN
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  197843. 14381
  197844. SATO, M.
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  197846. A_DIELS
  197847. ALDER REACTIONS ASYMMETRIC SYNTHESIS ADDITIONS 1,3
  197848. DIOXIN
  197849. ONES STEREOSELECTIVITY 
  197850. PURE 
  197851. 15390N
  197852. 2/28/96
  197853. METHYL
  197854. 2,3,4,5
  197855. TETRAHYDRO
  197856. OXAZEPIN
  197857. ONE and THE DIOXEPINONE ANALOGUE 
  197858.  DIASTEREOFACIAL SELECTIVITY IN CATALYTIC HYDROGENATION and THE EXPLANATION
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  197860. 14382
  197861. MINISCI, F.
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  197864. 2/28/96
  197865. AiREACTIVITY OF CARBAMOYL RADICALS 
  197866.  THE FirST GENERAL and CONVENIENT FREE
  197867. RADICAL SYNTHESIS OF ISOCYANATES
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  197869. 14383
  197870. A    Su, C. C.B
  197871. JACSM
  197872. 15392N
  197873. 2/28/96
  197874. DIRECT APPROACH TO PALLADIUM
  197875. MEDIATED CYCLOADDITION. FIRST SINGLE
  197876. CRYSTAL STRUCTURE and CONVENIENT SYNTHESIS OF ZWITTERIONIC h3
  197877. TRIMETHYLENEMETHANE
  197878. PALLADIUM FROM NUCLEOPHILIC ADDITION OF CARBANIONS to AN ALLENYL COMPLEX
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  197880. 5000Y
  197881. 14384
  197882. TROST, B. M.
  197883. JACSM
  197884. 15393
  197885. 2/28/96
  197886. BUTENOLIDE SYNTHESIS BASED UPON A CONTRA
  197887. ELECTRONIC ADDITION IN A RUTHENIUM
  197888. CATALYZED ALDER ENE REACTION. SYNTHESIS and ABSOLUTE CONFIGURATION OF (+)
  197889. ANCEPSENOLIDE
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  197891. 4986Y
  197892. 14385
  197893. MAJETICH, G.
  197894. JACSM
  197895. 15394N
  197896. 2/28/96
  197897. A%CONCISE SYNTHESIS OF (+/
  197898. PEROVSKONE
  197899. 1994X    4979
  197900. 4980Y
  197901. 14386
  197902. Wang, Z.B
  197903. JACSM
  197904. 15395N
  197905. 2/28/96
  197906. APSYNTHESIS OF THE TETRACYCLIC MITOMYCIN SKELETON VIA A DIALKYLVINYLSULFONIUM SALT
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  197908. 4978Y
  197909. 14387
  197910. VELDKAMP, A.
  197911. JACSC
  197912. CATALYZED ASYMMETRIC DIHYDROXYLATION 
  197913. OSMIUM TETRAOXIDE ORGANOMETALLIC COMPOUNDS CIS
  197914. DIHYDROXYLATION MOLECULAR
  197915. STRUCTURE ALKALOID 
  197916. LIGANDS 
  197917. BASIS
  197918. SETS 
  197919. TETROXIDE COMPLEXES ENERGIES M
  197920. 15396N
  197921. 2/28/96
  197922. AdMECHANISM OF THE ENANTIOSELECTIVE DIHYDROXYLATION OF OLEFINS BY OSO4 IN THE PRESENCE OF CHIRAL BASES
  197923. 1994X    4937
  197924. 4946Y
  197925. 14388
  197926. COMINS, D. L.
  197927. METHOXYPYRIDINIUM SALTS N
  197928. ACYLDIHYDROPYRIDONES STEREOSELECTIVE SYNTHESIS ALKALOIDS (+/
  197929. SOLENOPSIN
  197930. A CHEMISTRY 
  197931. ESTERS 
  197932. 15397N
  197933. 2/28/96
  197934. ASYMMETRIC SYNTHESIS OF 2
  197935. ALKYL(ARYL)
  197936. DIHYDRO
  197937. PYRIDONES BY ADDITION OF GRIGNARD REAGENTS to CHIRAL 1
  197938. METHOXYPYRIDINIUM SALTS
  197939. 1994X    4719
  197940. 4728Y
  197941. 14389
  197942. WILLIAMS, J. P.
  197943. SODIUM BOROHYDRIDE PANICULATINE
  197944. TYPE TRIS(TRIMETHYLSILYL)SILANE CONSTRUCTION 
  197945. CYCLIZATION 
  197946. REDUCTIONS 
  197947. ALCOHOLS 
  197948. RADICALS 
  197949. KETONES 
  197950. MODEL M
  197951. 15398N
  197952. 2/28/96
  197953. AvTOTAL SYNTHESIS OF THE LYCOPODIUM ALKALOIDS MAGELLANINE and MAGELLANINONE BY THREE
  197954. FOLD ANNULATION OF 2
  197955. CYCLOPENTENONE
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  197958. 14390
  197959. MARTIN, S. F.
  197960. FORMAL TOTAL SYNTHESIS ASYMMETRIC TOTAL SYNTHESIS ENANTIOSELECTIVE ALDOL CONDENSATIONS 
  197961. METHYL 
  197962. CHIRAL ALDEHYDES STEREOSELECTIVE SYNTHESIS NATURAL PRODUCTS ERYTHROMYCIN
  197963. ACYCLIC STEREOSELECTION DIASTEREOFACIAL SELECTIVITY CARBONYL COMPOUNDS
  197964. 15399N
  197965. 2/28/96
  197966. AhSTRATEGIES FOR MACROLIDE SYNTHESIS. A CONCISE APPROACH to PROTECTED SECO
  197967. ACIDS OF ERYTHRONOLIDES A and B
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  197969. 4688Y
  197970. 14391
  197971. TANEMURA, K.
  197972. Chem. Lett.C
  197973. ACETALS 
  197974. CATALYST 
  197975. MILD M
  197976. 15400N
  197977. 2/28/96
  197978. ANDEPROTECTION OF 1,3
  197979. DITHIANES BY 2,3
  197980. DICHLORO
  197981. DICYANO
  197982. BENZOQUINONE (DDQ)
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  197984. 14392
  197985. MIYAKE, H.
  197986. Chem. Lett.
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  197988. ASYMMETRIC INDUCTION TRANSMETALATION 
  197989. BUSNCL3 
  197990. 15401N
  197991. 2/28/96
  197992. SELECTIVE SYNTHESIS OF HOMOALLYLIC ALCOHOLS VIA 2
  197993. ALKENYLATION OF ALDEHYDES BY 1
  197994. (TRIBUTYLSTANNYL)
  197995. ALKENE
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  197999. Chem. Lett.
  198000. AnDIELS
  198001. ALDER REACTIONS FUSED NITROGEN HETEROCYCLES N
  198002. AMINO
  198003. DIHYDRODIAZINEDIONES 
  198004. CONDENSATION 
  198005. REACTIVITY 
  198006. 15402N
  198007. 2/28/96
  198008. HETEROANNULATION OF A,b
  198009. UNSATURATED CARBENE COMPLEXES. [3+2] DIPOLAR CYCLOADDITION OF METHOXY(A,b
  198010. ALKYNYL)TUNGSTEN CARBENE COMPLEXES WITH 1,3
  198011. THIAZOLIUM
  198012. OLATES
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  198015. MATSUBARA, S.
  198016. Chem. Lett.CnGRIGNARD REAGENTS CARBONYL COMPOUNDS ORGANOLITHIUM 
  198017. AMINO ACIDS DIMETHYLHYDRAZONES ALKYLATION 
  198018. REVERSAL 
  198019. BOND M
  198020. 15403N
  198021. 2/28/96
  198022. A|DIASTEREOSELECTIVE ADDITION OF ORGANOMETALLIC REAGENTS to IMINES OR HYDRAZONES CONTAINING 1,3
  198023. OXATHIANE AS A CHIRAL TEMPLATE
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  198025. 14395
  198026. MATSUBARA, S.
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  198028. REAGENTS CYANOTRIMETHYLSILANE DIASTEREOSELECTIVITY NITRILES 
  198029. ALDOL M
  198030. 15404N
  198031. 2/28/96
  198032. LANTHANOID TRIFLATE CATALYZED CONJUGATE ADDITION OF AMINES to A,b
  198033. UNSATURATED ESTERS. A FACILE ROUTE to OPTICALLY ACTIVE b
  198034. LACTAM
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  198037. HOPF, H.
  198038. Chem. Ber.
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  198040. THERMAL PROPARGYL
  198041. COPE REACTION 1,5
  198042. HEXADIYNE
  198043. DIOL CYCLOBUTENE
  198044. DIACETYL FRAGMENTATIONS
  198045. RETRO
  198046. TANDEM REACTIONS 
  198047. PERICYCLIC REACTIONS 
  198048. 15405N
  198049. 2/28/96
  198050. ApTHERMAL REARRANGEMENTS .22. THE PROPARGYL
  198051. COPE REARRANGEMENT OF MESO and D/L
  198052. DIMETHYL
  198053. HEXADIYNE
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  198056. GROSCHL, D.
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  198060. ALDER REACTIONS CHEMOSELECTIVITY REGIOSELECTIVITY STEREOSELECTIVITY BENZOTHIETE 
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  198062. 2/28/96
  198063. AVCYCLOADDITION REACTIONS OF 2H
  198064. BENZO[B]THIETE and COMPOUNDS WITH CUMULATED DOUBLE BONDS
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  198068. Chem. Ber.
  198069. AZONIAALLENE CATIONS 
  198070. ISOCYANATES 4,5
  198071. DIHYDRO
  198072. 1,2,4
  198073. TRIAZOLIUM SALTS CINNOLINIUM SALTS CYCLOADDITIONS CALCULATIONS
  198074. MOLECULAR STRUCTURE HETEROELEMENT FUNCTIONS GEMINAL AZOELEMENT CYANAMIDIUM SALTS 
  198075. 15407N
  198076. 2/28/96
  198077. A>ON THE REACTION OF 1
  198078. AZONIAALLENE SALTS WITH ISOCYANATES
  198079. 1994X
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  198081. ADAM, W.
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  198084. 2/28/96
  198085. A]RING CLEAVAGE OF BENZOFURANS and TETRAHYDROBENZOFURANS BY M
  198086. CHLOROPERBENZOIC ACID EPOXIDATION
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  198089. BOTT, K.
  198090. Chem. Ber.
  198091. ETHYLENEDIAZONIUM SALTS
  198092. THERMAL STABILITY OF
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  198094. GENERATION OF
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  198096. INTERCEPTION OF 
  198097. KINETICS 
  198098. VINYL CATIONS REARRANGEMENT 
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  198100. 2/28/96
  198101. AJGENERATION OF 2
  198102. SUBSTITUTED 1
  198103. ETHENYL CATIONS FROM ETHYLENEDIAZONIUM SALTS
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  198106. A    FUNKE, F.
  198107. Chem. Ber.
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  198110. ALKYNYLCARBENE)
  198111. CHROMIUM COMPLEXES 2H
  198112. PYRROLES 
  198113. CYCLIZATION OF {[2
  198114. (METHYLENE AMINO) ETHENYL] CARBENE} CHROMIUM COMPLEXES TRANSITION METAL COMPLEXES 
  198115. CHROMIUM CARBENE COMPLEXES 
  198116. M = CR 
  198117. ORGANIC SYNTHESES (b
  198118. AMINOVINYL)CARBENE COMPLEXES 
  198119. 15410N
  198120. 2/28/96
  198121. MICHAEL ADDITION OF IMINES to ALKYNYLCARBENE COMPLEXES WITH SUBSEQUENT INTRAMOLECULAR CYCLIZATION 
  198122.  AN EFFICIENT 3
  198123. STEP SYNTHESIS OF 2H
  198124. PYRROLES
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  198127. IPAKTSCHI, J.
  198128. Chem. Ber.
  198129. ALLYLTRIBUTYLSTANNANE TRIMETHYLSILYL CYANIDE a,b
  198130. EPOXY ALDEHYDES CHELATION CONTROLLED ADDITION DIASTEREOSELECTIVITY PERCHLORATE
  198131. DIETHYL ETHER DIELS
  198132. ALDER REACTIONS LITHIUM PERCHLORATE 
  198133. ALLYLIC ALCOHOLS 
  198134. CHIRAL a,b
  198135. EPOXYALDEHYDES 
  198136. 15411N
  198137. 2/28/96
  198138. AECHELATE
  198139. CONTROLLED DIASTEREOSELECTIVE ADDITION to A,b
  198140. EPOXY ALDEHYDES
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  198143. YADAV, J. S.
  198144. Tet. Lett.C
  198145. TAXOL SKELETON SYSTEM 
  198146. A HIGHLY REGIOSELECTIVE REDUCTION OF EPOXY ALLYLIC ALCOHOLS TO CHIRAL BUTADIENYL ALCOHOLS AND ITS APPLICATION TO TAXOL SKELETON IS DESCRIBED.
  198147. 15412N
  198148. 2/28/96
  198149. AFAN EXPEDITIOUS APPROACH to THE SYNTHESIS OF CHIRAL BUTADIENYL ALCOHOLS
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  198154. Tet. Lett.C
  198155. ASYMMETRIC SYNTHESIS ANTITUMOR ACTIVITY TOPOISOMERASE
  198156. 1 DERIVATIVES (+/
  198157. CAMPTOTHECIN (S)
  198158. CAMPTOTHECIN INHIBITION 
  198159. ANALOGS 
  198160. AGENTS 
  198161. A9A CONVERGENT SYNTHESIS OF (+/
  198162. )CAMPTOTHECIN IS DESCRIBED.
  198163. 15413N
  198164. 2/28/96
  198165. A(REGIOSELECTIVE SYNTHESIS OF CAMPTOTHECIN
  198166. 1994 X    3613
  198167. 3616Y
  198168. 14405
  198169. A    Ko, S. Y.B
  198170. Tet. Lett.
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  198172. EPOXY SULFOXIDES CYCLIC SULFATES 
  198173. OLEFINS 
  198174. DISPARLURE 
  198175. PHEROMONES 
  198176. LIGANDS 
  198177. DISPARLURE, CONTAINING AN ISOLATED CIS
  198178. EPOXIDE FUNCTIONAL GROUP, WAS SYNTHESIZED EMPLOYING THE ASYMMETRIC DIHYDROXYLATION AND CYCLIC SULFATE REARRANGEMENT
  198179. OPENING REACTIONS AS THE KEY STEPS.
  198180. 15414N
  198181. 2/28/96
  198182. A]CIS
  198183. EPOXIDES VIA SHARPLESS' ASYMMETRIC DIHYDROXYLATION REACTION:  SYNTHESIS OF (+)
  198184. DISPARLURE
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  198186. 3604Y
  198187. 14406
  198188. EASTON, C. J.
  198189. Tet. Lett.
  198190. THE ISOXAZOLINES 2A, 2B AND 8 OBTAINED FROM NITRILE OXIDE CYCLOADDITIONS TO CYCLOHEX
  198191.  ENONE 1A AND ITS ANALOGUES 1B AND 7 REACTED WITH NICKEL PEROXIDE TO GIVE THE ISOXAZOLES 3A, 3B AND 9. IN CONTRAST, THE CORRESPONDING 2
  198192. BROMOCYCLOHEX
  198193. ENONES 4A, 4B AND 10, PREPARED BY BROMINATION OF THE CORRESPONDING ALKENES LA, 1B AND 7, UNDERWENT NITRILE OXIDE CYCLOADDITIONS TO AFFORD THE REGIOISOMERIC ISOXAZOLES 6A, 6B AND 12, RESPECTIVELY.
  198194. 15415N
  198195. 2/28/96
  198196. AYREVERSAL OF REGIOCHEMISTRY IN THE SYNTHESIS OF ISOXAZOLES BY NITRILE OXIDE CYCLOADDITIONS
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  198198. 3592Y
  198199. 14407
  198200. BAILEY, P. D.
  198201. Tet. Lett.
  198202. RUNDER CONDITIONS OF KINETIC CONTROL, THE CIS
  198203. DIASTEREOSELECTIVITY OF THE PICTET
  198204. SPENGLER REACTION BETWEEN TRYPTOPHAN ESTERS AND ALDEHYDES CAN BE CONTROLLED BY VARYING THE SIZE OF THE ESTER GROUP;  THE REACTION PROCEEDS IN ESSENTIALLY QUANTITATIVE YIELD WITH MOST ALDEHYDES WHEN CONDUCTED IN CHLOROFORM IN THE PRESENCE OF MOLECULAR SIEVES.
  198205. 15416N
  198206. 2/28/96
  198207. ENHANCING THE YIELD and DIASTEREOSELECTIVITY OF THE PICTET
  198208. SPENGLER REACTION:  A HIGHLY EFFICIENT ROUTE to CIS
  198209. DISUBSTITUTED TETRAHYDRO
  198210. CARBOLINES
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  198212. 3588Y
  198213. 14408
  198214. BAILEY, P. D.
  198215. Tet. Lett.
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  198217. SPENGLER REACTION ALKALOIDS 
  198218. THE b
  198219. NITRILE 2, WHICH IS AN ADVANCED INTERMEDIATE FOR THE SYNTHESIS OF SEVERAL INDOLE ALKALOIDS, IS COMPOSED OF A MIXTURE OF ENOL/KETO TAUTOMERS, AND OF DIASTEREOISOMERS;  NEVERTHELESS, REDUCTION WITH SODIUM BOROHYDRIDE YIELDS ESSENTIALLY A SINGLE DIASTEREOISOMER 3.
  198220. 15417N
  198221. 2/28/96
  198222. STEREOSPECIFIC REDUCTION OF A b
  198223. NITRILE:  FORMATION OF A SINGLE INDOLIC b
  198224. HYDROXY
  198225. NITRILE FROM A MIXTURE OF TAUTOMERS and DIASTEREOISOMERS
  198226. 1994 X    3585
  198227. 3586Y
  198228. 14409
  198229. CHEN, S. T.
  198230. Tet. Lett.C:PHASE
  198231. TRANSFER REAGENTS ALCOHOLS 
  198232. PEPTIDES 
  198233. ESTERS 
  198234. ACIDS 
  198235. VINYL GROUP OF VINYL ALKYLATE (C=2 OR 16) AND VINYL BENZOATE HAVE BEEN FOUND TO BE A GOOD LEAVING GROUP IN ACYLATION OF ALCOHOLS (40
  198236. 50% YIELD) AND AMINES (IN 60
  198237. 90% YIELD).
  198238. 15418N
  198239. 2/28/96
  198240. ASVINYL CARBOXYLATE, AN ACYLATING REAGENT FOR SELECTIVE ACYLATION OF AMINES and DIOLS
  198241. 1994 X    3583
  198242. 3584Y
  198243. 14410
  198244. YANG, T. K.
  198245. Tet. Lett.
  198246. &THE STEREOSELECTIVE CYCLIZATION OF AN a
  198247. CYANOAMINE CONTAINING A VINYL GROUP INDUCED BY TICL4 IN A METHYLENE CHLORIDE SOLUTION, PRODUCES CIS 2,6
  198248. DIALKYLPIPERIDINE;  WHEREAS A SIMILAR REACTION OF AN a
  198249. CYANOAMINE CONTAINING A SILYL SUBSTITUTED VINYL GROUP GAVE THE CORRESPONDING TRANS ISOMER ONLY.
  198250. 15419N
  198251. 2/28/96
  198252. A~STEREOSELECTIVE SYNTHESIS OF 2,6
  198253. DISUBSTITUTED PIPERIDINE ALKALOIDS VIA TICL4 INDUCED IMINIUM ION CYCLIZATION OF A
  198254. CYANOAMINES
  198255. 1994X    3581
  198256. 3582Y
  198257. 14411
  198258. KITA, Y.
  198259. Tet. Lett.C
  198260. ACETIC ANHYDRIDE SULFOXIDES 
  198261. ETHOXY VINYL ESTER IS A NOVEL EFFICIENT REAGENT FOR THE ASYMMETRIC PUMMERER REACTION HAVING HIGH ENANTIOSELECTIVITY AND HIGH YIELD.
  198262. 15420N
  198263. 2/28/96
  198264. ABA NOVEL ASYMMETRIC PUMMERER REACTION INDUCED BY ETHOXY VINYL ESTER
  198265. 1994X    3575
  198266. 3576Y
  198267. 14412
  198268. TOMINAGA, Y.
  198269. Tet. Lett.CITHIOCARBONYL YLIDE ORGANIC SYNTHESIS FLUORIDE
  198270. ION DERIVATIVES GENERATION 
  198271. (TRIMETHYLSILYLMETHYLTHIO)(METHYLTHIO)METHYLENE
  198272. INDANEDIONE(1), READILY PREPARED BY REACTION OF 2
  198273. BIS(METHYLTHIO)METHYLENE
  198274. INDANEDIONE(9) WITH TRIMETHYLSILYLMETHYL MERCAPTANE(10), WAS SHOWN TO BE THE SYNTHETIC EQUIVALENT OF ALKYLIDENE
  198275. THIOCARBONYL YLIDE. TREATMENT OF THIS COMPOUND WITH FLUORIDE IONS IN THE PRESENCE OF REACTIVE HETERO
  198276. DIPOLAROPHILES SUCH AS CARBONYL COMPOUNDS AND ACTIVE ALKENES AFFORDED 1,3
  198277. DIPOLAR CYCLOADDUCTS, 2
  198278. ALKYLIDEN
  198279. OXATHIOLANES AND 2
  198280. ALKYLIDENETHIOPHEB)NES, BY CARBONYL
  198281. SUBSTITUTED COUNTERPARTS
  198282. 15421N
  198283. 2/28/96
  198284. SILYLMETHYL
  198285. SUBSTITUTED KETENE DITHIOACETALS AS SYNTHETIC EQUIVALENT OF A NOVEL 1,3
  198286. DIPOLAR REAGENT, ALKYLIDENETHIOCARBONYL YLIDE;  SYNTHESIS and [3+2] CYCLOADDITION REACTIONS
  198287. 1994X    3555
  198288. 3558Y
  198289. 14413
  198290. Abe, M.B
  198291. Tet. Lett.C"CYCLOADDITION PHOTOCHEMISTRY
  198292. TCNE 
  198293. UNSATURATED EsTERS WERE FORMED FROM CYCLOPROPANONE ACETALS IN THE REACTION WITH DDQ OR CHLORANIL, WHERE RING
  198294. OPENED C
  198295. C AND C
  198296. O BONDED ADDUCTS WERE THE INTERMEDIATES FORMED VIA A SET MECHANISM RESULTING IN THE EsTER FORMATION.
  198297. 15422N
  198298. 2/28/96
  198299. FORMATION OF UNSATURATED ESTERS IN THE SINGLE ELECTRON TRANSFER REACTION OF CYCLOPROPANONE ACETALS WITH QUINONES UNDER NON
  198300. IRRADIATED CONDITIONS
  198301. 1994X    3551
  198302. 3554Y
  198303. 14414
  198304. Lai, L. L.B
  198305. Tet. Lett.C
  198306. DEMETHYLATION 
  198307. ANALOGS 
  198308. A NEW METHOD WAS DEVELOPED FOR SYNTHESIS OF AROMATIC HETEROTRICYCLIC COMPOUNDS IN 50
  198309. 64% YIELDS FROM DIARYLS BEARING A FUNCTIONALITY INCLUDING OME, COOME, AND CN, AND A LEAVING GROUP (I.E., F AND OME) BY USE OF ME3SISNA IN 1,3
  198310. DIMETHYL
  198311. IMIDAZOLIDINONE AT 120
  198312. 15423N
  198313. 2/28/96
  198314. AhSODIUM TRIMETHYLSILANETHIOLATE IN NOVEL CYCLIZATIONS FOR SYNTHESIS OF AROMATIC HETEROTRICYCLIC COMPOUNDS
  198315. 1994X    3545
  198316. 3546Y
  198317. 14415
  198318. GRANDJEAN, D.
  198319. Tet. Lett.CYTRIPHENYLPHOSPHINE DIBROMIDE 
  198320. BROMIDES 
  198321. CYCLIZATION 
  198322. CONVERSION 
  198323. ACETALS 
  198324. ETHERS 
  198325. ACCESS 
  198326. DIBROMOALKENES, 1
  198327. BROMOALKYNES AND ALKYNES COULD BE OBTAINED IN EXCELLENT YIELDS BY HOMOLOGATION OF FUNCTIONNALIZED ALDEHYDES THROUGH A MODIFIED MCKELVIE
  198328. COREY PROCEDURE.
  198329. 15424N
  198330. 2/28/96
  198331. AnAN IMPROVED PROCEDURE FOR ALDEHYDE
  198332. ALKYNE HOMOLOGATION VIA 1,1
  198333. DIBROMOALKENES;  SYNTHESIS OF 1
  198334. BROMOALKYNES
  198335. 1994X    3529
  198336. 3530Y
  198337. 14416
  198338. A    DALLA, V.
  198339. Tet. Lett.
  198340. SILVER CATALYZED CYCLIZATION 
  198341. ALKYLIDENE 
  198342. LACTONES 
  198343. EXOCYCLIC ENOL LACTONES 3
  198344. HYDROXY
  198345. METHYLENE BUTYROLACTONES b
  198346. HYDROXY
  198347. ACETYLENIC ACIDS 
  198348. SPIROKETALS 
  198349. CYCLIZATION
  198350. THE TITLE COMPOUND WAS OBTAINED IN 4 STEPS WITH AN OVERALL YIELD OF 64% WITH THE SILVER
  198351. CATALYZED CYCLIZATION OF THE CORRESPONDING SUBSTITUTED b
  198352.  HYDROXY
  198353.  ACETYLENIC ACID AS THE KEY STEP.
  198354. 15425N
  198355. 2/28/96
  198356. SILVER
  198357. CATALYZED HETEROCYCLIZATION:  FIRST TOTAL SYNTHESIS OF THE NATURALLY OCCURRING CIS-2
  198358. HEXADECYL
  198359. HYDROXY
  198360. METHYLENE BUTYROLACTONE
  198361. 1994X    3525
  198362. 3528Y
  198363. 14417
  198364. STOLLE, A.
  198365. Tet. Lett.
  198366. PAUSON
  198367. KHAND REACTION
  198368. INTRAMOLECULAR METHYLENECYCLOPROPANES DOUBLE BOND ACTIVATION IN SPIRO{CYCLOPROPANE
  198369. BICYCLO[3.3.0]OCT
  198370. ONES} 
  198371. ENANTIOMERICALLY PURE COMPOUNDS STEREOSELECTION 
  198372. FORMAL SYNTHESIS BICYCLO[3.3.0]OCTENONES CYCLIZATIONS 
  198373. COMPLEXES 
  198374. INTRAMOLECULAR PAUSON
  198375. KHAND REACTIONS OF 1,6
  198376. ENYNES 3A
  198377. C WITH A METHYLENE CYCLOPROPANE TERMINATOR AND A CHIRAL ACETAL MOIETY ADJACENT TO THE TRIPLE BOND GAVE SPIRO{CYCLOPROPANE
  198378. BICYCLO[3.3.0]OCT
  198379. ONES} 5A
  198380. C IN GOOD YIELDS WITH A DIASTEREOSELECTIVITY OF UP TO 6.4: 1. THE MAJOR DIASTEREOMER OF 5B WAS CONVERTED TO ENANTIOMERICALLY PURE BICYCLO[3.3.0]OCTANE
  198381. DIONE 8, WHICH SHOWED A NEGATIVE PEAK AT 287 NM IN THE CD CURVE, CONSISTENT WITH AN ASSUMED (5R) CONFIGURATION.
  198382. 15426N
  198383. 2/28/96
  198384. AWENANTIOSELECTIVE CONSTRUCTION OF SPIRO{CYCLOPROPANE
  198385. BICYCLO[3.3.0]OCT
  198386. ONES}
  198387. 1994X    3521
  198388. 3524Y
  198389. 14418
  198390. STOLLE, A.
  198391. Tet. Lett.
  198392. PAUSON
  198393. KHAND REACTIOn INTRAMOLECULAR METHYLENECYCLOPROPANES DOUBLE BOND ACTIVATION IN BICYCLO[3.3.0]OCT
  198394. ONES SPIROCYCLOPROPANE DERIVATIVES 
  198395. CYCLOPROPYL BUILDING
  198396. BLOCKS 1
  198397. ALKENYLCYCLOPROPYL ESTERS 
  198398. ORGANIC SYNTHESIS SUBSTITUTIONS 
  198399. CYCLIZATIONS 
  198400. ALKYNE 
  198401. CYCLOPROPYLIDENE
  198402. HEXYNES LIKE 2, E. G. PREPARED VIA PALLADIUM(0)
  198403. CATALYZED SUBSTITUTION OF 1
  198404. ETHENYL CYCLOPROPYL SULFONATES 1, UNDERGO AN INTRAMOLECULAR PAUSON
  198405. KHAND REACTION BOTH EFFICIENTLY AND REGIOSELECTIVELY.
  198406. 15427N
  198407. 2/28/96
  198408. AXTHE VIRTUE OF METHYLENECYCLOPROPANE TERMINATORS IN INTRAMOLECULAR PAUSON
  198409. KHAND REACTIONS
  198410. 1994X    3517
  198411. 3520Y
  198412. 14419
  198413. OPPOLZER, W.
  198414. Tet. Lett.C^AMINO ACIDS 
  198415. LEWIS
  198416. ACIDS 
  198417. ALPHA CATALYSTS CAB ENANTIOSELECTIVITY AUXILIARIES 
  198418. CAMPHOR 
  198419. DIENES 
  198420. sR2ALCL
  198421. COORDINATED N
  198422. METHACRYLOYLSULTAM IC UNDERGOES EFFICIENT, ENDO
  198423. SELECTIVE AND HIGHLY DIASTEREOFACE CONTROLLED [4+2]
  198424. ADDITIONS TO CYCLOPENTADIENE, ISOPRENE, (E)
  198425. PIPERYLENE AND THE 2
  198426. SILYLOXYDIENES 10 AND 12. THE RESULTING CRYSTALLINE CYCLOADDUCTS ARE SMOOTHLY REDUCED WITH LIALH4 PROVIDING THE RECOVERED AUXILIARY AND THE CORRESPONDING ENANTIOMERICALLY PURE ALCOHOLS.
  198427. 15428N
  198428. 2/28/96
  198429. AMASYMMETRIC DIELS
  198430. ALDER REACTIONS CHIRAL N
  198431. METHACRYLOYLSULTAMS WITH 1,3
  198432. DIENES
  198433. 1994X    3509
  198434. 3512Y
  198435. 14420
  198436. ROTH, K. D.
  198437. Tet. Lett.CTPROPARGYL CATIONS NICHOLAS REACTION 
  198438. COBALT NUCLEOPHILES COMPLEXES 
  198439. INDOLES 
  198440. AMINES 
  198441. REACTIONS OF MOLYBDENUM STABILIZED PROPARGYL CATIONS 2 WITH ENAMINES ARE DESCRIBED, CONSTITUTING A MOLYBDENUM MEDIATED ANALOGUE OF THE NICHOLAS REACTION AND EXTENDING THE SCOPE OF PROPARGYLATIONS OF ENAMINES BY MEANS OF TRANSITION METAL COMPLEXED CARBOCATIONS.
  198442. 15429N
  198443. 2/28/96
  198444. AJTRANSITION METAL MEDIATED THREE COMPONENT COUPLING REACTIONS WITH ENAMINES
  198445. 1994X    3505
  198446. 3508Y
  198447. 14421
  198448. A    KONIG, B.
  198449. Tet. Lett.
  198450. AyMETAL GUEST CATIONS MOLECULAR RECOGNITION ANTITUMOR ANTIBIOTICS 
  198451. SITES 
  198452. CHEMISTRY 
  198453. DYNEMICIN COMPLEX SYSTEM 
  198454. ALKALI 
  198455. THE SYNTHESIS OF A NEW BIS(CROWN ETHER)
  198456. ENEDIYNE 3 VIA PALLADIUM CATALYZED COUPLING REACTIONS IS DESCRIBED. ON TREATMENT WITH SODIUM
  198457. HEXAFLUOROPHOSPHATE TWO CATIONS ARE BOUND BY THE TITLE COMPOUND 3;  WITH POTASSIUM IONS THE SANDWICH COMPLEX 5 IS FORMED. THE THERMAL REACTIVITY OF THE ENEDIYNE MOIETY TOWARDS CYCLISATION WAS INVESTIGATED BY DIFFERENTIAL SCANNING CALORIMETRY, WHEREBY THE METAL COMPLEXES SHOWED AN INCREASED STABILITY.
  198458. 15430N
  198459. 2/28/96
  198460. A?SYNTHESIS and REACTIVITY OF THE FIRST BIS(CROWN ETHER) ENEDIYNE
  198461. 1994X    3501
  198462. 3504Y
  198463. 14422
  198464. Kim, N. S.B
  198465. Tet. Lett.C
  198466. 1-PYRROLINE ANNULATION PYRROLIZIDINE ALKALOIDS LINKED OLIGOSACCHARIDES CYCLOADDITION (+)
  198467. CASTANOSPERMINE CASTANOSPERMINE INHIBITORS 
  198468. SUPINIDINE (
  198469. SWAINSONINE (
  198470. SLAFRAMINE 
  198471. A SHORT, ENANTIOSELECTIVE SYNTHESIS OF 6,7
  198472. DIEPICASTANOSPERMINE (4) HAS BEEN ACHIEVED BY AN INTRAMOLECULAR AZIDE
  198473. DIENE 1,3
  198474. DIPOLAR CYCLOADDITION, FOLLOWED BY RING
  198475. OPENING OF THE VINYLAZIRIDINE 6 AND SUBSEQUENT DIHYDROXYLATION.
  198476. 15431N
  198477. 2/28/96
  198478. AzAN AZIDE
  198479. DIENE CYCLOADDITION APPROACH to INDOLIZIDINE ALKALOIDS. AN ENANTIOSELECTIVE SYNTHESIS OF 6,7
  198480. DIEPICASTANOSPERMINE
  198481. 1994X    3489
  198482. 3492Y
  198483. 14423
  198484. VANHESSCHE, K. P. M. 
  198485. Tet. Lett.C
  198486. ACID 
  198487. 'aSYMMETRIC DIHYDROXYLATION (AD) OF PRIMARY ALLYLIC HALIDES IS DESCRIBED. ENANTIOMERIC EXCESSES RANGE FROM 40 TO 98%. SUBSEQUENT BASE TREATMENT GIVES EPOXY ALCOHOLS IN HIGH YIELDS. THIS STRATEGY IS FURTHER ILLUSTRATED BY THE SYNTHESIS OF (
  198488. DIEPOXYBUTANE, AN IMPORTANT C
  198489. CHIRAL BUILDING BLOCK.
  198490. 15432N
  198491. 2/28/96
  198492. AbASYMMETRIC DIHYDROXYLATION OF PRIMARY ALLYLIC HALIDES and A CONCISE SYNTHESIS OF (
  198493. DIEPOXYBUTANE
  198494. 1994X    3469
  198495. 3472Y
  198496. 14424
  198497. SNIECKUS, V.
  198498. Tet. Lett.C
  198499. ELECTROPHILIC FLUORINATIONS POLYSUBSTITUTED AROMATICS CESIUM FLUOROXYSULFATE SUBSTITUTION 
  198500. REAGENT BENZENEDISULFONIMIDE MONOFLUORINATION METHODOLOGY 
  198501. REGIOSPECIFIC FLUORINATION USING N
  198502. FLUOROBENZENESULFONIMIDE (FSI) AND N
  198503. FLUORO
  198504. BENZENE DISULFONIMIDE (NFOBS) REAGENTS VIA DIRECTED ORTHO METALATION (SCHEME 1) IS REPORTED AND EXCEPTIONS OF PHSO2 TRANFER FROM NFSI ARE DESCRIBED.
  198505. 15433N
  198506. 2/28/96
  198507. AfDIRECTED ORTHO METALATION 
  198508.  MEDIATED F+ INTRODUCTION. REGIOSPECIFIC SYNTHESIS OF FLUORINATED AROMATICS
  198509. 1994X    3465
  198510. 3468Y
  198511. 14425
  198512. POSS, K. M.
  198513. Tet. Lett.CHASYMMETRIC OXIDATION CHIRAL SULFOXIDES OXAZIRIDINES 
  198514. CHEMISTRY 
  198515. REAGENT 
  198516. A{THE SYNTHESIS AND DIASTEREOSELECTIVE OXIDATION OF NOVEL TETRAHYDROMEVINIC ACID LACTONE SULFIDES TO SULFOXIDES IS DESCRIBED.
  198517. 15434N
  198518. 2/28/96
  198519. AnDIASTEREOSELECTIVE OXIDATION OF SULFIDES to SULFOXIDES. SYNTHESIS OF NOVEL C
  198520. 6 SULFOXY TETRAHYDROMEVINIC ACIDS
  198521. 1994X    3461
  198522. 3464Y
  198523. 14426
  198524. WEBB, K. S.
  198525. Tet. Lett.
  198526. SEVERAL SULFIDES HAVE BEEN CONVERTED TO SULFOXIDES OR SULFONES IN MODEST TO EXCELLENT YIELDS. THE OXIDANT WAS OXONE
  198527.  AND THE REACTIONS WERE PERFORMED IN 12.5% AQUEOUS ACETONE AND BUFFERED TO PH 7.5 
  198528.  8.0 WITH SODIUM BICARBONATE.
  198529. 15435N
  198530. 2/28/96
  198531. A7A MILD, INEXPENSIVE and PRACTICAL OXIDATION OF SULFIDES
  198532. 1994X    3457
  198533. 3460Y
  198534. 14427
  198535. HONG, C. Y.
  198536. Tet. Lett.C
  198537. ALKALOIDS 
  198538. PALLADIUM CATALYZED CYCLIZATION OF HYDROISOQUINOLINE DIENE 10 TO AFFORD THE PENTACYCLIC OPIATE 11 IS THE CENTRAL STEP IN A NEW SYNTHESIS OF OPIUM ALKALOIDS.
  198539. 15436N
  198540. 2/28/96
  198541. AjPREPARATION OF OPIUM ALKALOIDS BY PALLADIUM CATALYZED BIS
  198542. CYCLIZATIONS. FORMAL TOTAL SYNTHESIS OF MORPHINE
  198543. 1994X    3453
  198544. 3456Y
  198545. 14428
  198546. A    Oh, J. H.B
  198547. Tet. Lett.C+TRANSFORMATIONS 
  198548. ALCOHOLS 
  198549. KETONES 
  198550. ETHERS 
  198551. AN EFFICIENT EXCISION OF THE KETO BRIDGE PRESENT IN TRICYCLO[4.3.1.1(2,5)]UNDECANONES OR TRICYCLO[5.3.1.1(2,6)]DODECANONES HAS BEEN ACCOMPLISHED BY b
  198552. FRAGMENTATION OF AN ALKOXY RADICAL UNDER THE PROCEDURE OF SUAREZ [PHI(OAC)2
  198553. 15437N
  198554. 2/28/96
  198555. AfSYNTHETIC STUDIES ON TAXOL .2. b
  198556. FRAGMENTATION OF ALKOXY RADICALS IN MEDIUM
  198557. SIZED CARBOCYCLE SYNTHESIS
  198558. 1994X    3449
  198559. 3452Y
  198560. 14429
  198561. GILLIGAN, P. J.
  198562. Tet. Lett.
  198563. AKDIPOLAR APROTIC MEDIA b
  198564. KETOESTERS 
  198565. SYNTHETIC APPLICATIONS MALONATE ESTERS 
  198566. THE REACTION OF DIMETHYL 2
  198567. BENZYLAZETIDIN
  198568. YL)PROPANE
  198569. DIOATE WITH NACN IN WET DMSO AT HIGH TEMPERATURE AFFORDED METHYL 2(1
  198570. BENZYLAZETIDIN
  198571. YL)ACETATE, WHEREAS SIMILAR TREATMENT WITH NACL GAVE METHYL 3
  198572. BENZYLAZABICYCLO
  198573. [3.1.0]HEXAN
  198574. ONE CARBOXYLATE. THESE RESULTS PROVIDE ADDITIONAL EVIDENCE THAT CHLORIDE
  198575.  AND CYANIDE
  198576. MEDIATED CLEAVAGES OF ESTERS MAY PROCEED BY DIFFERENT MECHANISMS.
  198577. 15438N
  198578. 2/28/96
  198579. AhDIVERGENT MECHANISMS FOR THE DEALKOXYCARBONYLATION OF A 2
  198580. AZETIDINYL)MALONATE BY CHLORIDE and CYANIDE
  198581. 1994X    3441
  198582. 3444Y
  198583. 14430
  198584. FOUBELO, F.
  198585. Tetrahedron
  198586. As(E)
  198587. LITHIO
  198588. TOSYLBUTENONE DIMETHYL KETAL ORGANIC SYNTHESIS 
  198589. ANION EQUIVALENT CYCLIZATION
  198590. DERIVATIVES 
  198591. RESONANCE 
  198592. THE REACTION OF (Z)
  198593. IODOACRYLIC ACID (1) WITH A SUBSTOICHIOMETRIC AMOUNT OF TRIBUTYLTIN CHLORIDE (1: 0.5 MOLAR RATIO) AND AN EXCESS OF SODIUM BOROHYDRIDE (1: 4 MOLAR RATIO) IN THE PRESENCE OF A CATALYTIC AMOUNT OF AIBN (1: 0.18 MOLAR RATIO) AND AN EXCESS OF AN ELECTROPHILIC OLEFIN (2) IN ETHANOL LEADS, AFTER TREATMENT WITH AQUEOUS SODIUM FLUORIDE, TO THE EXPECTED FUNCTIONALISED (E)
  198594. UNSATURATED CARBOXYLIC ACIDS 3 IN A STEREOSELECTIVE MANNER. THE PROBABLE REACTION MECHANISM INVOLVES FRB
  198595. EE RADICAL INTERMEDIATES.
  198596. 15439N
  198597. 2/28/96
  198598. ACYLVINYL INTERMOLECULAR RADICAL ADDITIONS to DOUBLE BONDS:  STEREOSELECTIVE SYNTHESIS OF FUNCTIONALISED (E)
  198599. UNSATURATED CARBOXYLIC ACIDS
  198600. 1994X    6715
  198601. 6720Y
  198602. 14431
  198603. CHIACCHIO, U.
  198604. Tetrahedron
  198605. SECONDARY ORBITAL INTERACTIONS 
  198606. DIELS
  198607. ALDER REACTIONS ISOXAZOLIDINIUM SALTS 1,3
  198608. CYCLOADDITION REGIOSELECTIVITY DIPOLAROPHILES 
  198609. ADDITIONS 
  198610. OXIDES 
  198611. ROUTE 
  198612. THE STEREOCHEMISTRY OF 1,3
  198613. DIPOLAR CYCLOADDITION OF C
  198614. METHYL
  198615. PHENYLNITRONE I WITH SUBSTITUTED STYRENES HAS BEEN INVESTIGATED. THE PRESENCE OF AN HYDROXYL FUNCTION AT THE ORTHO POSITION LT THE DIPOLAROPHILE COMPLETELY CONTROLS THE STEREOCHEMICAL COURSE OF THE REACTION WITH THE EXCLUSIVE FORMATION OF CYCLOADDUCT 7. MNDO CALCULATIONS HELP TO RATIONALISE THE OBTAINED RESULTS ON THE BASIS OF AN INTERMOLECULAR HYDROGEN BONDING, WHICH LEADS TO CHANGES IRT THE FMO PROPERTIES SO IMPROVING A STABIB2LIZING SECONDARY ORBITAL INTERACTION IN THE E
  198616. 15440N
  198617. 2/28/96
  198618. AXSTEREOSELECTIVE CONTROL IN 1,3
  198619. DIPOLAR CYCLOADDITION OF NITRONES to SUBSTITUTED STYRENES
  198620. 1994X    6671
  198621. 6680Y
  198622. 14432
  198623. BELL, D.
  198624. Tetrahedron
  198625. UNSATURATED ESTERS STEREOCHEMICAL CONTROL CARBONYL COMPOUNDS CHELATION CONTROL PSEUDOMONIC ACID OLEFINATION CHEMISTRY DERIVATIVES 
  198626. CARBANIONS 
  198627. ABSENCE 
  198628. THE E: Z SELECTIVITY IN THE INTRODUCTION OF THE TRI
  198629. SUBSTITUTED DOUBLE BOND IN BRL 49467 COULD BE CONTROLLED BY THE CHOICE OF BASE AND SILYL GROUP USED IN A PETERSON OLEFINATION REACTION. THE METHOD ALLOWING OPTIMUM E
  198630. SELECTIVITY WAS DEVELOPED SUCH THAT IT COULD BE SCALED UP TO 100MMOL.
  198631. 15441N
  198632. 2/28/96
  198633. AVSTEREOSELECTIVITY IN THE PETERSON REACTION 
  198634.  APPLICATION to THE SYNTHESIS OF BRL 49467
  198635. 1994X    6643
  198636. 6652Y
  198637. 14433
  198638. DAVIES, S. G.
  198639. TetrahedronC
  198640. NUCLEAR MAGNETIC RESONANCE 
  198641. ACYCLIC STEREOSELECTION ABSOLUTE CONFIGURATION CONDENSATION 
  198642. ALDEHYDES 
  198643. ASSEMBLAGE 
  198644. LACTONES 
  198645. ACID 
  198646. DIBUTYLBORON ENOLATES OF 1,3
  198647. DIACYLIMIDAZOLIDINE
  198648. THIONES AND 1,3
  198649. DIACYLIMIDAZOLIDIN
  198650. ONES UNDERGO HIGHLY SYN
  198651. STEREOSELECTIVE ALDOL REACTIONS WITH ALDEHYDES TO ALLOW ELABORATION OF BOTH ACYL SIDECHAINS. THE REACTION IS PROPOSED TO OCCUR VIA SEQUENTIAL ENOLISATION RATHER THAN VIA A BISENOLATE AND THE STEREOCHEMISTRY OF THE PRODUCT WAS ELUCIDATED BY BOTH X
  198652. RAY CRYSTALLOGRAPHY AND REDUCTIVE CLEAVAGE OF A HOMOCHIRAL ALDOL PRODUCT TO GIVE (1R,2S)
  198653. PHENYL
  198654. METHYLPROPANE
  198655. DIOL. IN CONTRASBCT, TIN (II) TRIFLATE MEDIATED ALDOL REACTIONS RESULT IN ONLY ONE OF
  198656. 15442N
  198657. 2/28/96
  198658. BIFUNCTIONAL CHIRAL AUXILIARIES .7. ALDOL REACTIONS OF ENOLATES DERIVED FROM 1,3
  198659. DIACYLIMIDAZOLIDINE
  198660. THIONES and 1,3
  198661. DIACYLIMIDAZOLIDIN
  198662. 1994X    6621
  198663. 6642Y
  198664. 14434
  198665. ALONSO, D. A.
  198666. TetrahedronCcUSEFUL REAGENT 2
  198667. (CHLOROMETHYL)
  198668. TOSYLPROPENE 
  198669. STEREOCHEMISTRY 1,3
  198670. REARRANGEMENT ALKENES 
  198671. DIANION 
  198672. DILITHIATED 2
  198673. (TOSYLMETHYL)
  198674. PROPEN
  198675. OL (6) FUNCTIONED AS A NUCLEOPHILE AT THE A
  198676. POSITION OF THE ALLYLIC ANION IN REACTIONS WITH DEUTERIUM OXIDE, ALKYL HALIDES, AND ALDEHYDES, AND IN CONJUGATE ADDITIONS TO A,b
  198677. UNSATURATED CARBONYL COMPOUNDS. WITH NITRO
  198678. OLEFINS CONJUGATE ADDITION OCCURRED AT THE g
  198679. POSITION OF THE ALLYLIC ANION. THE HYDROXY ESTER DERIVED BY REACTION WITH TERT
  198680. BUTYL BROMOACETATE WAS CONVERTED INTO A VARIETY OF SYNTHETICALLY USEFUL DIENIC AND b,g
  198681. UNSATURATED d
  198682. LACTONES. THE B%REDUCTIVE DETOSYLATION OF SOME OF THE
  198683. 15443N
  198684. 2/28/96
  198685. AkTOSYLATED LITHIUM 2
  198686. (LITHIOMETHYL)
  198687. PROPEN
  198688. OLATE:  A g
  198689. ALKOXIDE ALLYL SULFONE ANION IN ORGANIC SYNTHESIS
  198690. 1994X    6603
  198691. 6620Y
  198692. 14435
  198693. DIEZ, A.
  198694. TetrahedronCnN
  198695. ALKYLPYRIDINIUM SALTS INDOLE ALKALOIDS NUCLEOPHILIC ADDITION REACTIVITY 
  198696. CHEMISTRY 
  198697. ENTRY 
  198698. DIHYDROPYRIDINES 
  198699. A NEW AND VERSATILE SYNTHESIS OF TETRACYCLIC COMPOUNDS 10, 22 AND 24 PRESENTING THE ABED RING SYSTEM OF STRYCHNOS ALKALOIDS IS DESCRIBED BY CLOSURE OF THE C
  198700. 11B BOND IN THE KEY STEP. THE INTERMEDIATE TETRAHYDROPYRIDINIUM SALTS 2 HAVE BEEN OBTAINED FROM 2
  198701. DITHIAN
  198702. YL)INDOLE (3) AND EITHER 2
  198703. CYANO
  198704. ETHYL
  198705. METHYL
  198706. 1,2,3,6
  198707. TETRAHYDRO PYRIDINE (4A) OR N
  198708. SUBSTITUTED d(3)
  198709. PIPERIDEIN
  198710. ONES (5).
  198711. 15444N
  198712. 2/28/96
  198713. SYNTHETIC APPLICATIONS OF 2
  198714. DITHIAN
  198715. YL)INDOLES .4. NEW SYNTHESIS OF THE TETRACYCLIC ABED RING SYSTEM OF STRYCHNOS ALKALOIDS
  198716. 1994X    6585
  198717. 6602Y
  198718. 14436
  198719. RANU, B. C.
  198720. TetrahedronC
  198721. SOLID
  198722. PHASE REACTION SURFACE MEDIATED REACTIONS 
  198723. MARKOVNIKOV 
  198724. HYDRATION 
  198725. DEPROTECTION METHOD REDUCTIVE CLEAVAGE ORGANIC REACTIONS 
  198726. MICHAEL REACTION 
  198727. ALUMINA 
  198728. ALCOHOLS 
  198729. HYDROBORATION 
  198730. A SIMPLE AND GENERAL PROCEDURE FOR HYDRATION OF UNACTIVATED ALKENES AND ALKYNES PRODUCING LESS SUBSTITUTED ALCOHOLS SELECTIVELY HAS BEEN ACHIEVED BY THE REACTION OF THE CORRESPONDING ALKENES OR ALKYNES ON SILICA GEL SUPPORT WITH ZINC BOROHYDRIDE IN 1,2
  198731. DIMETHOXYETHANE.
  198732. 15445N
  198733. 2/28/96
  198734. AgSILICA GEL SUPPORTED ZINC BOROHYDRIDE. A NOVEL REAGENT FOR HYDRATION OF UNACTIVATED ALKENES and ALKYNES
  198735. X    6579
  198736. 6584Y
  198737. 14437
  198738. VORBRUGGEN, H.
  198739. TetrahedronC:PYRROLE CHEMISTRY DERIVATIVES 
  198740. ISOCYANATE 
  198741. REAGENT 
  198742. ROUTE 
  198743. ADDITION OF CHLOROSULFONYLISOCYANATE (CSI) TO HETEROCYCLES SUCH AS THIOPHENE (4) OR INDOLE (15) AND UNSATURATED SYSTEMS SUCH AS DIHYDROPYRAN (7) GIVES N
  198744. CHLOROSULFONYL AMIDES RCONHSO2CL, WHICH CAN BE CONVERTED BY EQUIVALENT AMOUNTS OF TRIETHYLAMINE TO THEIR CORRESPONDING NITRILES. SINCE CARBOXYLIC ACIDS REACT WITH CSI TO N
  198745. CHLOROSULFONYL AMIDES, SUBSEQUENT TREATMENT WITH TRIETHYLAMINE AFFORDS THE CORRESPONDING NITRILES, BUT NO ISOCYANATES AS CLAIMED BY OTHER AUTHORS. THE MECHANISMS OF THE B5CONVERSION OF THE INTERMEDIATE N
  198746. CHLOROSULFONYLAMIDES
  198747. 15446N
  198748. 2/28/96
  198749. THE INTRODUCTION OF NITRILE
  198750. GROUPS INTO HETEROCYCLES AND CONVERSION OF CARBOXYLIC GROUPS INTO THEIR CORRESPONDING NITRILES WITH CHLOROSULFONYLISOCYANATE and TRIETHYLAMINE
  198751. 1994X    6549
  198752. 6558Y
  198753. 14438
  198754. DEKHANE, M.
  198755. Tetrahedron
  198756. BENZODIAZEPINE RECEPTOR ANTAGONIST METHOXY
  198757. METHYLAMIDES STREPTOMYCES
  198758. LAVENDULAE AMINO ACIDS LAVENDAMYCIN 
  198759. CARBOLINES 
  198760. ESTER DERIVATIVES OXIDATION 
  198761. ANALOGS 
  198762. ETHYL b
  198763. CARBOLINE
  198764. CARBOXYLATE (9) AND METHYL 4
  198765. METHYL
  198766. CARBOLINE
  198767.  CARBOXYLATE (15) WERE PREPARED IN HIGH YIELDS HY CONDENSING INDOLE
  198768. CARBOXALDEHYDE (5) (ITSELF PREPARED BY LITHIUM ALUMINUM HYDRIDE REDUCTION OF THE WEINREB AMIDE DERIVED FROM INDOLE
  198769. CARBOXYLIC ACID) WITH ETHYL 2
  198770. AMINO
  198771. DIETHOXYPROPIONATE (6) AND METHYL 2
  198772. AMINO
  198773. DIETHOXYBUTYRATE (12), RESPECTIVELY, FOLLOWED BY REDUCTION OF THE IMINE BONDS FORMED WITH SODIUM CYANOBOROHYDRIDE AND CYCLIZATION OF THE RESULTING AMINB9ES (8 AND 14, RESPECTIVELY) USING TITANIUM (IV) CHLORIDE.
  198774. 15447N
  198775. 2/28/96
  198776. A NEW EFFICIENT SYNTHESIS OF ETHYL b
  198777. CARBOLINE
  198778. CARBOXYLATE (b
  198779. CCE) and METHYL 4
  198780. METHYL
  198781. CARBOLINE
  198782. CARBOXYLATE (4
  198783. METHYL
  198784. CCM) STARTING FROM INDOLE
  198785. 2-CARBOXALDEHYDE
  198786. 1994X    6299
  198787. 6306Y
  198788. 14439
  198789. ALAZARD, J. P.
  198790. TetrahedronC
  198791. ASYMMETRIC SYNTHESIS CARBON 
  198792. THE REACTION OF THE OXAZOLOPIPERIDONES 8, 10 (OR THE OXAZOLOPIPERIDINE 12) WITH THE MIXTURE TMSOTF
  198793. TMSCN (OR TBDMSOTF
  198794. TMSCN) IN THE PRESENCE OF ZNBR2, DID NOT LEAD BY IRREVERSIBLE RING OPENING TO THE CORRESPONDING A
  198795. CYANOAMIDES (OR A
  198796. CYANO AMINE) AS EXPECTED. IN CONTRAST, REVERSIBLE RING OPENING TAKES PLACE LEADING TO THE THERMODYNAMICAL PRODUCTS. IN THE CASE OF 17, THE PARTICIPATION OF THE AMIDE GROUP IN VARIOUS EXPERIMENTAL CONDITIONS LEADS TO NEW HETEROCYCLES LIKE THE IMINE 18 AND THE AB
  198797. MINOETHER 22.
  198798. 15448N
  198799. 2/28/96
  198800. AESYNTHESIS and REACTIVITY OF OXAZOLOPIPERIDINES AND OXAZOLOPIPERIDONES
  198801. 1994X    6287
  198802. 6298Y
  198803. 14440
  198804. MCKINSTRY, L.
  198805. Tetrahedron
  198806. AWDIELS
  198807. ALDER REACTION LEWIS
  198808. ACIDS 
  198809. COMPLEXES HYDROGENATION 
  198810. INDUCTION 
  198811. ALDEHYDES 
  198812. ALPHA 
  198813. &THE USE OF BISPHOSPHINE LIGANDS RELATED TO DIOP AS CHIRAL MODIFIERS IN THE RH(I) CATALYZED [4+2] CYCLOISOMERIZATION REACTION RESULTS IN MODERATE TO GOOD LEVELS OF ENANTIOSELECTION. THE MODE OF ABSOLUTE STEREOINDUCTION IS SUBJECT TO ELECTRONIC AND TORSIONAL MODIFICATION OF THE CHELATING LIGAND.
  198814. 15449N
  198815. 2/28/96
  198816. ON THE ASYMMETRIC RH(I) CATALYZED [4+2] CYCLOISOMERIZATION REACTION. ELECTRONIC and TORSIONAL LIGAND CONTROL OF ABSOLUTE STEREOSELECTION
  198817. 1994X    6145
  198818. 6154Y
  198819. 14441
  198820. HUTCHINSON, K. D.
  198821. Tetrahedron
  198822. THE STRUCTURES OF TWO NOVEL SPIROPENTANOPYRROLIZIDINE OXIME ALKALOIDS, NAMELY 2',3',5',6',7',7A'
  198823. HEXAHYDRO
  198824. DIMETHYLSPIRO[CYCLOPENTANE
  198825. PYRROLIZINE]
  198826. OXIME (1) AND 2',3',5',6',7',7A'
  198827. HEXAHYDRO
  198828. DIMETHYLSPIRO [CYCLOPENTANE
  198829. [1H] PYRROLIZINE]
  198830. OXIME
  198831. METHYL ETHER (2) HAVE BEEN CONFIRMED BY SYNTHESIS. THE ROUTE INVOLVED SYNTHESIS OF NITROPOLYZONAMINE (4), A KNOWN MILLIPEDE ALKALOID, FROM 2,2
  198832. DIMETHYLCYCLOPENTANONE IN 6 STEPS. AFTER CONVERSION OF 4 TO THE KETONE 6, THE B,OXIME 1 AND O
  198833. METHYL OXIME 2 WERE OBTAINED. 
  198834. 15450N
  198835. 2/28/96
  198836. A\SYNTHESIS OF PYRROLIZIDINE OXIMES 222 and 236:  NOVEL ALKALOIDS OF A DENDROBATID POISON FROG
  198837. 1994X    6129
  198838. 6136Y
  198839. 14442
  198840. CAPOZZI, G.
  198841. B    Synthesis
  198842. PHTHALIMIDESULFENYL CHLORIDE ADDITION TO ARYLALKYNES BENZO[B]THIOPHENES NAPHTHOTHIOPHENES THIENOTHEIOPHENES PHTHALIMIDOSULFENYL CHLORIDE 
  198843. ACETYLENES 
  198844. DERIVATIVES 
  198845. 15451N
  198846. 2/28/96
  198847. ArPHTHALIMIDESULFENYL CHLORIDE .7. SYNTHESIS OF 2
  198848. SUBSTITUTED 3
  198849. CHLOROBENZO[B]THIOPHENES and RELATED HETEROAROMATICS
  198850. 1994X
  198851. 14443
  198852. HITZLER, M. G.
  198853. B    Synthesis
  198854. AZONIAALLENE SALTS CYCLOADDITIONS 
  198855. OLEFINS 
  198856. ACETYLENES 2
  198857. AZONIAALLENE SALTS BENZOPHENANTHRIDINESM
  198858. 15452N
  198859. 2/28/96
  198860. AWON THE REACTION OF 1,3
  198861. DICHLORO
  198862. AZONIAALLENE SALTS WITH OLEFINS and DIPHENYLACETYLENE
  198863. 1994X
  198864. 14444
  198865. KATRITZKY, A. R.
  198866. B    Synthesis
  198867. BENZOTRIAZOLE NUCLEOPHILIC SUBSTITUTION SUBSTITUTED BENZOTRIAZOLYLMETHANES A
  198868.  AND A
  198869. TRISUBSTITUTED ETHERS A
  198870.  AND A
  198871. TRISUBSTITUTED SULFIDES AUXILIARY 
  198872. 15453N
  198873. 2/28/96
  198874. ARBENZOTRIAZOLE
  198875. MEDIATED SYNTHESIS OF A
  198876.  AND A
  198877. TRISUBSTITUTED ETHERS and SULFIDES
  198878. 1994X
  198879. 14445
  198880. MOUSSOUNGA, J.
  198881. B    Synthesis
  198882. A<KETENE DITHIOACETALS N,S
  198883. ACETALS 
  198884. ACETALS 
  198885. ESTERS 
  198886. KETO 
  198887. 15454N
  198888. 2/28/96
  198889. A1NEW TWO
  198890. STEP SYNTHESIS OF A
  198891. OXOKETENE O,N
  198892. ACETALS
  198893. 1994X
  198894. 14446
  198895. Wang, X. H.B    Synthesis
  198896. A?HBR TRIPHENYLPHOSPHINE ADDUCT 
  198897. THERMOLYSIS 
  198898. BUTYL BROMIDE 
  198899. 15455N
  198900. 2/28/96
  198901. ACA CONVENIENT and ECONOMIC WAY to PRODUCE ANHYDROUS HYDROGEN BROMIDE
  198902. 1994X
  198903. 14447
  198904. Hwu, J. R.B    Synthesis
  198905. NITRATE ESTERS 
  198906. ALKYL P
  198907. TOLUENESULFONATES SODIUM NITRATE TETRA
  198908. BUTYLAMMONIUM NITRATE 
  198909. PHASE
  198910. TRANSFER CATALYSIS THERMAL DECOMPOSITION ENERGETIC MATERIALS KINETICS 
  198911. ALCOHOLS 
  198912. 15456N
  198913. 2/28/96
  198914. A6PRACTICAL METHOD FOR THE PREPARATION OF NITRATE ESTERS
  198915. 1994X
  198916. 14448
  198917. AUBERSON, Y. P.
  198918. B    SynthesisM
  198919. 15457N
  198920. 2/28/96
  198921. AgBENZAZEPINEDIONES BY THE REACTION OF ANTHRANILIDES UNDER VILSMEIER
  198922. HAACK CONDITIONS:  A REINVESTIGATION
  198923. 1994X
  198924. 14449
  198925. A    Wu, Y. K.B    SynthesisCK5
  198926. PENTANONE LEVULINATE 
  198927. IODONATION
  198928.  IODIDE 
  198929. IODOACETAL
  198930. INTERMEDIATE M
  198931. 15458N
  198932. 2/28/96
  198933. AJCONVENIENT PROCEDURE FOR PREPARING 2
  198934. IODOPROPYL)
  198935. METHYL
  198936. DIOXOLANE
  198937. 1994X
  198938. 14450
  198939. KOBAYASHI, S.
  198940. B    SynthesisC
  198941. HIGHLY STEREOSELECTIVE ALLYLATION 
  198942. ORGANO
  198943. SILICON COMPOUNDS FUNCTIONALIZED KETONES COMPLEX CARBOCYCLES FACILE CHEMISTRY MAGNESIUM M
  198944. 15459N
  198945. 2/28/96
  198946. POT SYNTHESIS OF HOMOALLYLIC ALCOHOLS FROM 1,3
  198947. DIENES: TANDEM VICINAL DIFUNCTIONALIZATION OF 1,3
  198948. DIENES BY HYDRIDE ADDITION
  198949. ALDEHYDE COUPLING SEQUENCE VIA ORGANOSILICON INTERMEDIATES
  198950. 1994X
  198951. 14451
  198952. KATRITZKY, A. R.
  198953. B    Synthesis
  198954. BENZOTRIAZOLE BENZOTRIAZOLYL ALKYLATION HETEROALKYLATION SUBSTITUTION NUCLEOPHILIC N
  198955. SUBSTITUTED BENZOTRIAZOLES 
  198956. VERSATILE AMIDOALKYLATION REAGENTS    
  198957. SODIUM BOROHYDRIDE REDUCTION A
  198958. AMIDOALKYLATION ELECTROORGANIC CHEMISTRY 
  198959. 15460N
  198960. 2/28/96
  198961. AoBENZOTRIAZOLE AS A SYNTHETIC AUXILIARY:  BENZOTRIAZOLYL ALKYLATIONS and BENZOTRIAZOLE
  198962. MEDIATED HETEROALKYLATION
  198963. 1994X
  198964. 14452
  198965. RAVIKUMAR, V. T.
  198966. Syn. Commun.CtANTISENSE OLIGONUCLEOTIDES 
  198967. PEPTIDE SYNTHESIS 
  198968. AGENTS CHLOROTRIMETHYLSILANE DEPROTECTION 
  198969. DIAMINES 
  198970. ANALOGS 
  198971. PHENOL M
  198972. 15461N
  198973. 2/28/96
  198974. A;A CONVENIENT LARGE SCALE SYNTHESIS OF N
  198975. ETHYLENEDIAMINE
  198976. 1994X    1767
  198977. 1772Y
  198978. 14453
  198979. Wang, R. X.B
  198980. Syn. Commun.M
  198981. 15462N
  198982. 2/28/96
  198983. A/A MODIFIED SYNTHESIS OF O
  198984. HYDROXYARYL ALDEHYDES
  198985. 1994X    1757
  198986. 1760Y
  198987. 14454
  198988. A    DEVAN, B.
  198989. Syn. Commun.C#CLAISEN REARRANGEMENT COPE 
  198990. ETHERS M
  198991. 15463N
  198992. 2/28/96
  198993. AcSYNTHESIS and MERCURY(II) TRIFLUOROACETATE MEDIATED CYCLIZATION OF N
  198994. ARYL N
  198995. ALLENYLMETHYL CARBAMIDE
  198996. 1994X    1691
  198997. 1700Y
  198998. 14455
  198999. HASSNER, A.
  199000. Syn. Commun.C<OLEFIN CYCLOADDITIONS NITRILE OXIDES 
  199001. ROUTE 
  199002. SUGARS 
  199003. ETHERS M
  199004. 15464N
  199005. 2/28/96
  199006. CYCLOADDITIONS .51. STEREOSELECTIVE FORMATION OF FUNCTIONALIZED 2
  199007. TETRAHYDROFURANS FROM AROMATIC ALDEHYDES VIA INTRAMOLECULAR 1,3
  199008. DIPOLAR CYCLOADDITIONS (INOC and IOOC)
  199009. 1994X    1669
  199010. 1682Y
  199011. 14456
  199012. A    PATRA, D.
  199013. Syn. Commun.
  199014. CzCITRUS MEALYBUG 
  199015. SEX PHEROMONE 
  199016. ORGANIC SYNTHESIS 
  199017. RISSO 
  199018. SESQUITERPENES CYCLOBUTANES 
  199019. ANNULATION 
  199020. SYSTEMS 
  199021. ETHERS 
  199022. ROUTE M
  199023. 15465N
  199024. 2/28/96
  199025. SEQUENTIAL [2+2] PHOTOCYCLOADDITION and REARRANGEMENT to SUBSTITUTED CYCLOPENTANONE 
  199026.  A FORMAL SYNTHESIS OF PLANOCOCCYL ACETATE
  199027. 1994X    1663
  199028. 1668Y
  199029. 14457
  199030. AHMAD, F. B. H.
  199031. Syn. Commun.M
  199032. 15466N
  199033. 2/28/96
  199034. AnISOMERISATION OF DIELS
  199035. ALDER ADDUCTS OF BENZOYL
  199036. BENZOQUINONES 
  199037.  A ROUTE to THE ANTHRACYCLINONE RING SYSTEM
  199038. X    1639
  199039. 1649Y
  199040. 14458
  199041. SUNDBERG, R. J.
  199042. Org. Prep. Proc. Int.M
  199043. 15467N
  199044. 2/28/96
  199045. A[OXIDATION OF AMINES BY DICHLORODICYANOQUINONE (DDQ) WITH TRAPPING BY TRIMETHYLSILYL CYANIDE
  199046. 1994X
  199047. 14459
  199048. PATNEY, H. K.
  199049. Org. Prep. Proc. Int.M
  199050. 15468N
  199051. 2/28/96
  199052. A9AN IMPROVED PROCEDURE FOR THE PREPARATION OF 1,3
  199053. DITHIANE
  199054. 1994X
  199055. 14460
  199056. ARGADE, N. P.
  199057. Org. Prep. Proc. Int.M
  199058. 15469N
  199059. 2/28/96
  199060. AyA NEW APPROACH to ALKYL 2
  199061. OXOQUINOLINE
  199062. ACETATES BY TRIPHENYLPHOSPHINE
  199063. INDUCED CYCLIZATION OF ALKYL O
  199064. FORMYLMALEANILATES
  199065. 1994X
  199066. 14461
  199067. CHRISTENSEN, J. B.
  199068. Org. Prep. Proc. Int.M
  199069. 15470N
  199070. 2/28/96
  199071. A9AN ECONOMICAL PREPARATION OF 2
  199072. BROMOETHYL)
  199073. DIOXANE
  199074. 1994X
  199075. 14462
  199076. DASZKIEWICZ, Z.
  199077. Org. Prep. Proc. Int.M
  199078. 15471N
  199079. 2/28/96
  199080. A=AN ALTERNATE METHOD FOR THE SYNTHESIS OF SECONDARY NITRAMINES
  199081. 1994X
  199082. 14463
  199083. VLASOVA, O. G.
  199084. Org. Prep. Proc. Int.M
  199085. 15472N
  199086. 2/28/96
  199087. A?A SIMPLE SYNTHESIS OF THE HETEROCYCLES S,S
  199088. DIPHENYLSULFILIMINES
  199089. 1994X
  199090. 14464
  199091. PANKOWSKI, J.
  199092. Org. Prep. Proc. Int.
  199093. 15473N
  199094. 2/28/96
  199095. A\A SIMPLE and EFFICIENT PREPARATION OF METHOXYMETHYL ESTERS OF PENICILLINS and CEPHALOSPORINS
  199096. 1994X
  199097. 14465
  199098. FORMAN, M. A.
  199099. Org. Prep. Proc. Int.M
  199100. 15474N
  199101. 2/28/96
  199102. A=THE SYNTHESIS and REACTIONS OF PRISMANES, RECENT DEVELOPMENTS
  199103. 1994X
  199104. 14466
  199105. BERTRAND, M. P.
  199106. Org. Prep. Proc. Int.C5ALKENE
  199107. RADICAL
  199108. SULFONE
  199109. CYCLIZATION
  199110. LACTAM
  199111. PYRROLIDINEM
  199112. 15475N
  199113. 2/28/96
  199114. AORECENT PROGRESS IN THE USE OF SULFONYL RADICALS IN ORGANIC SYNTHESIS 
  199115.  A REVIEW
  199116. 1994X
  199117. 14467
  199118. Ito, H.B
  199119. ZIRCONOCENE EQUIVALENT ALLYLIC ZIRCONIUM SPECIES G
  199120. ALKOXY ALLYLIC ZIRCONIUM SPECIES 
  199121. ALLENIC ZIRCONIUM SPECIES DEALLYLATION 
  199122. RING CONTRACTION REACTION OXETANOCIN 
  199123. CARBON ANALOGUE MACRONECINE 
  199124. CHIRAL IMINE 
  199125. COUPLING REACTION 
  199126. 15476N
  199127. 2/28/96
  199128. AhDEVELOPMENT OF NEW SYNTHETIC METHODOLOGY BASED ON ZIRCONIUM
  199129. MEDIATED CARBON CARBON BOND FORMING REACTION
  199130. 1994X
  199131. 14468
  199132. HOSHINO, O.
  199133. 15477N
  199134. 2/28/96
  199135. TOTAL SYNTHESIS OF MONTANINE
  199136. TYPE AMARYLLIDACEAE ALKALOIDS, (+/
  199137. MONTANINE, (+/
  199138. COCCININE, (+/
  199139. PANCRACINE, and (+/
  199140. BRUNSVIGINE
  199141. 1994X
  199142. 14469
  199143. KODAMA, H.
  199144. CYCLOPROPANE AMINO ACIDS 
  199145. AMINO ACIDS 
  199146. ASYMMETRIC SYNTHESIS BIOACTIVE PEPTIDES ENKEPHALIN 
  199147. ENZYME 
  199148. INHIBITORS 
  199149. ALGA GRATELOUPIA
  199150. CARNOSA ETHYLENE BIOSYNTHESIS 1
  199151. AMINOCYCLOPROPANE
  199152. CARBOXYLIC ACID 1
  199153. AMINOCYCLOPROPANECARBOXYLIC ACID M
  199154. 15478N
  199155. 2/28/96
  199156. ArSYNTHESIS OF CYCLOPROPANE AMINO ACIDS and THEIR INCORPORATION INTO BIOACTIVE PEPTIDES AS CONFORMATIONAL CONSTRAINT
  199157. 1994 X
  199158. 14470
  199159. KOSKINEN, A. M. P.
  199160.  (VOL 58, PG 4480, 1993)M
  199161. 15479N
  199162. 2/28/96
  199163. A7ASYMMETRIC CATALYSIS IN INTRAMOLECULAR CYCLOPROPANATION
  199164. 1994X
  199165. 2914Y
  199166. 14471
  199167. CASIRAGHI, G.
  199168. 15480N
  199169. 2/28/96
  199170. AETOTAL SYNTHESES OF ALL FOUR ISOMERS OF CIS
  199171. DIHYDROXYPYRROLIZIDINE
  199172. 1994X    2906
  199173. 2909Y
  199174. 14472
  199175. PATONAY, T.
  199176. 15481N
  199177. 2/28/96
  199178. A5A GENERAL and EFFICIENT SYNTHESIS OF A
  199179. AZICAO KETONES
  199180. 1994X    2902
  199181. 2905Y
  199182. 14473
  199183. NADER, B. S.
  199184. 15482N
  199185. 2/28/96
  199186. AfA NOVEL FLUORIDE ION MEDIATED OLEFINATION OF ELECTRON
  199187. DEFICIENT ARYL KETONES BY ALKANESULFONYL HALIDES
  199188. 1994X    2898
  199189. 2901Y
  199190. 14474
  199191. CECCHERELLI, P.
  199192. 15483N
  199193. 2/28/96
  199194. ALMETAL
  199195. CATALYZED, INTRAMOLECULAR REACTIONS OF A
  199196. DIAZO KETONES WITH ISOXAZOLES
  199197. 1994X    2882
  199198. 2884Y
  199199. 14475
  199200. MILLER, D. C.
  199201. 15484N
  199202. 2/28/96
  199203. A^SYNTHESIS and CHARACTERIZATION OF NEW ''EXPANDED'' THIOPHENE
  199204.  and FURAN
  199205. CONTAINING MACROCYCLES
  199206. 1994X    2877
  199207. 2879Y
  199208. 14476
  199209. BENATI, L.
  199210. JOCCyDIPHENYL DISULFIDE CYCLIZATION 
  199211. QUINOLINES 
  199212. ROUTE POLYAZAPENTADIENES THERMOLYSIS 
  199213. DERIVATIVES 
  199214. MECHANISM 
  199215. SULFIDES 
  199216. ARYL M
  199217. 15485N
  199218. 2/28/96
  199219. AiFREE
  199220. RADICAL ADDITION OF ALKANETHIOLS to ALKYNES. REARRANGEMENTS OF THE INTERMEDIATE b
  199221. THIOVINYL RADICALS
  199222. 1994X    2818
  199223. 2823Y
  199224. 14477
  199225. MONN, J. A.
  199226. COBALT MEDIATED CYCLIZATION PAUSON
  199227. KHAND REACTION (
  199228. KAINIC ACID (
  199229. KAINIC ACID ENANTIOSELECTIVE SYNTHESIS 
  199230. FORMAL SYNTHESIS 
  199231. KAINOIDS 
  199232. ROUTE 
  199233. METHYLENATION 
  199234. 15486N
  199235. 2/28/96
  199236. ADA CONCISE, STEREOCONTROLLED THIAZOLIUM YLIDE APPROACH to KAINIC ACID
  199237. 1994X    2773
  199238. 2778Y
  199239. 14478
  199240. DESMARTEAU, D. D.
  199241. JOCCfOXAZIRIDINES 
  199242. ALBENDAZOLE 
  199243. OXIDATION 
  199244. CHEMISTRY DIMETHYLDIOXIRANE METABOLITE 
  199245. DIOXIRANES 
  199246. SHEEP 
  199247. RATS M
  199248. 15487N
  199249. 2/28/96
  199250. AnMILD and SELECTIVE OXYGENATION OF SULFIDES to SULFOXIDES AND SULFONES BY PERFLUORO
  199251. DIALKYLOXAZIRIDINES
  199252. 1994X    2762
  199253. 2765Y
  199254. 14479
  199255. KATRITZKY, A. R.
  199256. BROMO KETONES N
  199257. VINYLIMINOPHOSPHORANES 
  199258. RING SYSTEM A,B
  199259. UNSATURATED KETONES ROUTE 
  199260. BENZOTRIAZOLE 
  199261. EQUIVALENT 
  199262. AMINES 
  199263. 15488N
  199264. 2/28/96
  199265. A5A NEW and SAFE APPROACH to (N
  199266. VINYLIMINO)PHOSPHORANES
  199267. 1994X    2740
  199268. 2742Y
  199269. 14480
  199270. ADAM, W.
  199271. DYE SENSITIZED PHOTOOXYGENATION PHOTOSENSITIZED OXYGENATION 1,2
  199272. DIOXETANE FORMATION ENE REACTIONS  DERIVATIVES  
  199273. MECHANISM 
  199274. SYSTEM STABILIZATION INTERMEDIATE CONVERSION M
  199275. 15489N
  199276. 2/28/96
  199277. OXIDATION OF N
  199278. ACYLINDOLES BY DIMETHYLDIOXIRANE and SINGLET OXYGEN:  SUBSTITUENT EFFECTS ON THERMALLY PERSISTENT INDOLE EPOXIDES AND DIOXETANES
  199279. 1994X    2733
  199280. 2739Y
  199281. 14481
  199282. ZIEGLER, F. E.
  199283. INDUCED EPOXIDE FRAGMENTATION 
  199284. ATOM TRANSFER 
  199285. CYCLIZATION 
  199286. VINYL EPOXIDES 
  199287. IODO EPOXIDES 
  199288. ALLYLOXY RADICALS CONVENIENT METHOD RING EXPANSION 
  199289. RATE CONSTANTS REARRANGEMENTS CYCLOPROPYLMETHYL 
  199290. 15490N
  199291. 2/28/96
  199292. TANDEM FRAGMENTATION OF CYCLOPROPYLCARBINYL/OXIRANYLCARBINYL RADICALS. ON THE REVERSIBILITY OF OXIRANYLCARBINYL/ALLYLOXYL RADICAL FORMATION
  199293. 1994X    2707
  199294. 2714Y
  199295. 14482
  199296. ADAM, W.
  199297. SINGLET OXYGEN 
  199298. ORGANIC SYNTHESIS ACETYLENIC ALCOHOLS COUPLING REACTIONS REAGENTS 
  199299. A-HYDROSTANNYLATION HYDRIDES 
  199300. KETONES 
  199301. OLEFINS 
  199302. 15491N
  199303. 2/28/96
  199304. STANNYL ALLYLIC ALCOHOLS THROUGH PHOTOOXYGENATION (SCHENCK REACTION) OF VINYLSTANNANES and REDUCTION OF THE RESULTING ALLYLIC HYDROPEROXIDES: SYNTHESIS and SELECTED TRANSFORMATIONS
  199305. 1994X    2695
  199306. 2699Y
  199307. 14483
  199308. Pal, S.B
  199309. EFFICIENT SYNTHESIS 
  199310. VINYL RADICALS 
  199311. RATE CONSTANTS 
  199312. BOND FORMATION 
  199313. RING CLOSURE REARRANGEMENT CONSTRUCTION 
  199314. DERIVATIVES 
  199315. FRAMEWORKS 
  199316. ARYLATION M
  199317. 15492N
  199318. 2/28/96
  199319. REGIOSELECTIVE ARYL RADICAL CYCLIZATION .1. STEREOCONTROLLED SYNTHESIS OF LINEARLY CONDENSED HYDROAROMATIC CARBOCYCLIC SYSTEMS THROUGH 6
  199320. RING CLOSURES
  199321. 1994X    2687
  199322. 2694Y
  199323. 14484
  199324. RAWAL, V. H.
  199325. ALKALOIDS M
  199326. 15493N
  199327. 2/28/96
  199328. A1A SHORT, STEREOCONTROLLED SYNTHESIS OF STRYCHNINE
  199329. 1994X    2685
  199330. 2686Y
  199331. 14485
  199332. PEARSON, W. H.
  199333. C.INTRAMOLECULAR SCHMIDT REACTION 
  199334. ALKYL AZIDES M
  199335. 15494N
  199336. 2/28/96
  199337. AF[3 + 2] and [3 + 3] CYCLOADDITIONS OF AZIDES WITH ALLYLIC CARBOCATIONS
  199338. 1994X    2682
  199339. 2684Y
  199340. 14486
  199341. NOZAKI, K.
  199342. JOCCeACYL CYANIDES 
  199343. ALKYNES 
  199344. CYCLIZATION 
  199345. BONDS 
  199346. CHLORIDES 
  199347. INSERTION 
  199348. CYANATION 
  199349. IODIDES 
  199350. OLEFINS 
  199351. ROUTE M
  199352. 15495N
  199353. 2/28/96
  199354. AiACYLCYANATION OF TERMINAL ACETYLENES:  PALLADIUM
  199355. CATALYZED ADDITION OF ARYLOYL CYANIDES to ARYLACETYLENES
  199356. 1994X    2679
  199357. 2681Y
  199358. 14487
  199359. MOLANDER, G. A.
  199360. HIGH OPTICAL PURITY B
  199361. ALKYL
  199362. BORABICYCLO[3.3.1]NONANE 
  199363. REPRESENTATIVE KETONES ORGANOBORANE REAGENTS SELECTIVE REDUCTIONS ASYMMETRIC REDUCTION BORONATE REDUCTION CARBONYL REDUCTION MONOISOPINOCAMPHEYLBORANE DIISOPINOCAMPHEYLBORANE 
  199364. 15496N
  199365. 2/28/96
  199366. HYDROBORATION/INTRAMOLECULAR REDUCTION OF ALLYL KETONES WITH (DIISOPINOCAMPHEYL)BORANE:  A CONVENIENT SYNTHESIS OF ENANTIOMERICALLY ENRICHED 1,4
  199367. DIOLS
  199368. 1994X    2676
  199369. 2678Y
  199370. 14488
  199371. PANEK, J. S.
  199372. CHIRAL (E)
  199373. CROTYLSILANES ADDITION REACTIONS  
  199374. LEWIS ACID 
  199375. DOUBLE STEREODIFFERENTIATION DIASTEREOFACIAL SELECTIVITY CONJUGATE ADDITION A
  199376. ALKOXY ANNULATION ALLYLSTANNANES 
  199377. ALLYLSILANES 
  199378. 15497N
  199379. 2/28/96
  199380. DIRECT AMINO
  199381. CROTYLSILYLATION OF ACHIRAL ACETALS and ALDEHYDES:  ASYMMETRIC SYNTHESIS OF HOMOALLYLIC AMINES and FUNCTIONALIZED PYRROLIDINES
  199382. 1994X    2674
  199383. 2675Y
  199384. 14489
  199385. A    TAKAI, K.
  199386. HYDROXY ESTERS POLYFUNCTIONAL ORGANOZINC REAGENTS 
  199387. RCU(CN)ZNI 
  199388. COPPER REAGENTS CHEMISTRY 
  199389. ALDEHYDES
  199390.  OLEFINS 
  199391. KETONES 
  199392. 15498N
  199393. 2/28/96
  199394. A DRAMATIC EFFECT OF A CATALYTIC AMOUNT OF LEAD ON THE SIMMONS
  199395. SMITH REACTION and FORMATION OF ALKYLZINC COMPOUNDS FROM IODOALKANES. REACTIVITY OF ZINC METAL:  ACTIVATION and DEACTIVATION
  199396. 1994X    2671
  199397. 2673Y
  199398. 14490
  199399. A    TAKAI, K.
  199400. STEREOSELECTIVE PREPARATION NEOPENTYLIDENE COMPLEXES 
  199401. CARBONYL 
  199402. METHYLENATION CHROMIUM(II) CHLORIDE REAGENTS 
  199403. ALKYLIDENATION 
  199404. ETHERS 
  199405. DERIVATIVES 
  199406. ALDEHYDES 
  199407. TANTALUM 
  199408. 15499N
  199409. 2/28/96
  199410. NOVEL CATALYTIC EFFECT OF LEAD ON THE REDUCTION OF A ZINC CARBENOID WITH ZINC METAL LEADING to A GEMINAL DIZINC COMPOUND. ACCELERATION OF THE WITTIG
  199411. TYPE OLEFINATION WITH THE RCHX2
  199412. TICL4
  199413. ZN SYSTEMS BY ADDITION OF LEAD
  199414. 1994X    2668
  199415. 2670Y
  199416. 14491
  199417. SNYDER, J. P.
  199418. x-RAY CRYSTAL STRUCTURE NUCLEAR MAGNETIC RESONANCE ORGANOCOPPER REAGENTS SUBSTITUTION REACTIONS COPPER CHEMISTRY REACTIVITY 
  199419. ISOCYANIDE 
  199420. COMPLEXES 
  199421. SODIUM 
  199422. DIMERS M
  199423. 15500N
  199424. 2/28/96
  199425. AyTHE STRUCTURE OF ''R2CU(CN)LI2'' LITHIUM CUPRATES:  LOWER
  199426. ORDER AGGREGATES OF GILMAN REAGENTS and ORGANOLITHIUM COMPOUNDS
  199427. 1994X    2665
  199428. 2667Y
  199429. 14492
  199430. PATIL, L. S.
  199431. Ind. J. Chem. Sect. BM
  199432. 15501N
  199433. 2/28/96
  199434. SYNTHESIS and ANTIMICROBIAL ACTIVITY OF SOME NEW SULPHONAMIDES FROM 3,5
  199435. DIHALO
  199436. ALKOXYANILINES, 3
  199437. ALKOXYANILINES and 3,4,5
  199438. TRIHALOANILINES
  199439. 1994X
  199440. 14493
  199441. Rao, C. P.B
  199442. Ind. J. Chem. Sect. BC
  199443. ARYL PROPARGYL ETHERS M
  199444. 15502N
  199445. 2/28/96
  199446. THE CLAISEN REARRANGEMENT OF 6
  199447. PROPARGYLOXYCOUMARINS 
  199448.  FORMATION OF PYRANOCOUMARINS OR FUROCOUMARINS and THEIR ANTIBACTERIAL ACTIVITY
  199449. 1994X
  199450. 14494
  199451. A    MAITI, S.
  199452. Ind. J. Chem. Sect. BC
  199453. SINGLET OXYGEN M
  199454. 15503N
  199455. 2/28/96
  199456. PHOTOOXIDATION OF A b
  199457. KETOESTER
  199458. 1994X
  199459. 14495
  199460. DESOUZA, E. P.
  199461. Ind. J. Chem. Sect. BC
  199462. PROPARGYL ETHERS REARRANGEMENT M
  199463. 15504N
  199464. 2/28/96
  199465. SYNTHESIS AND BIOLOGICAL ACTIVITY OF NOVEL 1(2H)
  199466. FURO[2,3
  199467. H]ISOQUINOLINONE, 1(2H)
  199468. PYRANO[2,3
  199469. H]ISOQUINOLINONE and 2H
  199470. PYRANO[2,3
  199471. H]ISOQUINOLINE
  199472. DIONE
  199473. 1994X
  199474. 14496
  199475. BANERJI, A.
  199476. Ind. J. Chem. Sect. BC
  199477. SPECTROSCOPY M
  199478. 15505N
  199479. 2/28/96
  199480. AOREACTION OF SODIUM NAPHTHALENIDE WITH N
  199481. METHYLOXINDOLE UNDER APROTIC CONDITIONS
  199482. 1994X
  199483. 14497
  199484. Pal, R.B
  199485. Ind. J. Chem. Sect. B
  199486. HALOGENOKETONES CHLOROACETIC ACID 1,2
  199487. DIBROMOETHANE 
  199488. 15506N
  199489. 2/28/96
  199490. HETEROCYCLIC SYSTEMS CONTAINING BRIDGEHEAD NITROGEN ATOM .77. SYNTHESES OF THIAZOLO[2,3
  199491. B]BENZO[F]QUINAZOLIN
  199492. 1(2H)
  199493. ONE and [1,3]THIAZINO[2,3
  199494. B]BENZO[F]QUINAZOLIN
  199495. 1(2H)
  199496. ONE, Two NOVEL and HITHERTO UNKNOWN HETEROCYCLIC SYSTEMS
  199497. 1994X
  199498. 14498
  199499. CARVER, F. J.
  199500. J.C.S. Chem. Commun.C
  199501. TEMPLATE SYNTHESIS LIGANDS M
  199502. 15507N
  199503. 2/28/96V#DIRECTED MACROCYCLISATION REACTIONSW
  199504. 1994X    1277
  199505. 1280Z
  199506. 14499
  199507. WADE, P. A.
  199508. J.C.S. Chem. Commun.C
  199509. SPIROPENTADIENE M
  199510. 15508N
  199511. 2/28/96
  199512. A-TRAPPING EVIDENCE FOR 1,2
  199513. DINITROSPIROPENTENE
  199514. 1994X    1263
  199515. 1264Z
  199516. 14500
  199517. COLOMBANI, D.
  199518. J.C.S. Chem. Commun.C%ORGANIC SYNTHESIS 
  199519. RADICAL REACTIONS M
  199520. 15509N
  199521. 2/28/96
  199522. A|SYNTHESIS OF A,b
  199523. EPOXYESTERS BY HOMOLYTICALLY INDUCED DECOMPOSITION OF DERIVATIVES OF ETHYL 2
  199524. HYDROPEROXYETHYL)PROPENOATE
  199525. 1994X    1259
  199526. 1260Z
  199527. 14501
  199528. Ono, N.B
  199529. J.C.S. Chem. Commun.C#HIGHLY EFFICIENT SYNTHESIS ANALOGS M
  199530. 15510N
  199531. 2/28/96
  199532. SYNTHESIS OF A KEY INTERMEDIATE FOR PREPARATION OF 4,5
  199533. DIDEHYDRO PROSTAGLANDINS CONTAINING AN ALLENYL SIDE
  199534. CHAIN GROUP VIA TWO
  199535. COMPONENT COUPLING PROCESS. SYNTHESIS OF ENPROSTIL
  199536. 1994X    1251
  199537. 1252Z
  199538. 14502
  199539. BALASUBRAMANIAN, T.
  199540. J.C.S. Chem. Commun.
  199541. AjDIELS
  199542. ALDER REACTIONS 2
  199543. VINYLINDOLES REARRANGEMENTS VINYLINDOLES
  199544.  DERIVATIVES 
  199545. ALKALOIDS
  199546.  INDOLES 
  199547. ACCESS 
  199548. 15511N
  199549. 2/28/96
  199550. AUTANDEM TRANSFORMATIONS OF N
  199551. ALKYL
  199552. ALLENYLMETHYLANILINES to N
  199553. ALKYL
  199554. ETHENYLINDOLES
  199555. 1994X    1237
  199556. 1238Z
  199557. 14503
  199558. WEIDENBRUCH, M.
  199559. J.C.S. Chem. Commun.
  199560. CZINTRAMOLECULAR STERIC INTERACTIONS 
  199561. SILICON COMPOUNDS TETRAMESITYLDISILENE PHOTOLYSIS 
  199562. 15512N
  199563. 2/28/96
  199564. DISILENE and SILYLENE ADDITIONS to THE DOUBLE BONDS OF ALKENES and 1,3
  199565. DIENES:  MOLECULAR STRUCTURE OF A [2+2] CYCLOADDITION PRODUCT
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  199567. 1234Z
  199568. 14504
  199569. JENKINS, I. D.
  199570. J.C.S. Chem. Commun.C\HYDROGEN ATOM ABSTRACTION 
  199571. BUTOXY RADICALS REACTIVITY 
  199572. MECHANISM 
  199573. REDUCTION 
  199574. XANTHATES M
  199575. 15513N
  199576. 2/28/96
  199577. A1OXYGEN
  199578. CARBON b
  199579. BOND EFFECTS IN RADICAL REACTIONS
  199580. 1994X    1227
  199581. 1228Z
  199582. 14505
  199583. AOYAGI, Y.
  199584. J.C.S. Chem. Commun.
  199585. AEEFFECTIVE ALDOL SYNTHESIS B
  199586. HYDROXY ESTERS REFORMATSKY REACTION ZINC 
  199587. 15514N
  199588. 2/28/96
  199589. A%LOW
  199590. VALENT TANTALUM
  199591. MEDIATED REACTION
  199592. 1994X    1225
  199593. 1226Z
  199594. 14506
  199595. DEKIMPE, N.
  199596. J.C.S. Chem. Commun.C
  199597. EPOXIDES 
  199598. RADICALS M
  199599. 15515N
  199600. 2/28/96
  199601. AJSONOCHEMICAL CLEAVAGE OF 2
  199602. (BROMOMETHYL)AZIRIDINES BY A ZINC
  199603. COPPER COUPLE
  199604. 1994X    1221
  199605. 1222Z
  199606. 14507
  199607. SUZUKI, M.
  199608. J.C.S. Chem. Commun.C;COORDINATED 
  199609. PHOSPHORUS COMPOUNDS 
  199610. CHEMISTRY 
  199611. ALKENES 
  199612. BONDM
  199613. 15516N
  199614. 2/28/96
  199615. A,ENE REACTIONS OF A PHOSPHAALKENE AS ENOPHILE
  199616. 1994X    1191
  199617. 1192Z
  199618. 14508
  199619. Liu, P. Y.B
  199620. J.C.S. Chem. Commun.CACARBONYL COMPOUNDS ADDITIONS STEREOSELECTIVITY REDUCTION 
  199621. KETALS M
  199622. 15517N
  199623. 2/28/96
  199624. AzFACIAL SELECTIVITY IN NUCLEOPHILIC REACTIONS OF SPIROCYCLIC KETONES CAN BE CONTROLLED BY A DISTANT, ORTHOGONAL DOUBLE BOND
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  199626. 1184Z
  199627. 14509
  199628. BHUVANESWARI, N.
  199629. J.C.S. Chem. Commun.M
  199630. 15518N
  199631. 2/28/96
  199632. A NEW ROUTE to O
  199633. ALLENYLPHENOLS
  199634. 1994X
  199635. 1177Z
  199636. 14510
  199637. TANKO, J. M.
  199638. J.C.S. Chem. Commun.CORADICAL ION PROBES GRIGNARD REAGENTS BENZOPHENONE MECHANISM 
  199639. ADDITIONS 
  199640. ANIONS M
  199641. 15519N
  199642. 2/28/96
  199643. UTILIZATION OF 1,1
  199644. DIMETHYL
  199645. BUTYLSPIRO[2,5]OCTA
  199646. ONE AS A 'HYPERSENSITIVE' PROBE FOR SINGLE ELECTRON TRANSFER to CARBONYL COMPOUNDS
  199647. 1994X    1165
  199648. 1166Z
  199649. 14511
  199650. Lam, W. W. Y.B
  199651. J.C.S. Chem. Commun.M
  199652. 15520N
  199653. 2/28/96
  199654. CHEMISTRY OF EXTRADIOL AROMATIC RING CLEAVAGE:  ISOLATION OF A STABLE DIENOL RING FISSION INTERMEDIATE and STEREOCHEMISTRY OF ITS ENZYMATIC HYDROLYTIC CLEAVAGE
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  199656. 1164Z
  199657. 14512
  199658. MUKAI, C.
  199659. HANAOKA
  199660. J.C.S. Chem. Commun.C
  199661. PROPARGYL CATIONS SYNTHETIC ROUTES CYCLIZATION TETRAHYDROFURANS TETRAHYDROPYRAN 
  199662.  EPOXIDE RING OPENING TETRAHYDROFURAN 
  199663. ENDO TRIG 
  199664. COBALT ALKYNE 
  199665. CATION COMPLEXM
  199666. 15521N
  199667. 2/28/96
  199668. STEREOCOMPLEMENTARY CONSTRUCTION OF 2
  199669. ETHYNYL
  199670. HYDROXYTETRAHYDROFURAN DERIVATIVES VIA ENDO
  199671. MODE RING CLOSURE OF 3,4
  199672. EPOXY
  199673. SUBSTITUTEDHEX
  199674. 1994X    1161
  199675. 1162Z
  199676. 14513
  199677. BOERE, R. T.
  199678. Can. J. Chem.CHELECTRONIC STRUCTURE NORBORNADIENE INTERCONVERSION DERIVATIVES 
  199679. OLEFINS M
  199680. 15522N
  199681. 2/28/96
  199682. ALKENE ADDUCTS OF CYCLIC THIAZENES. IDENTIFICATION OF EXO AND ENDO ADDITION OF 1,3,2,4,6
  199683. DITHIATRIAZINES to 1,5
  199684. NORBORNADIENE BY 2D NMR METHODS and THE CRYSTAL STRUCTURE OF A SINGLE MOLECULE IN WHICH BOTH MODES OF ADDITION ARE DISPLAYED
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  199686. 1180Y
  199687. 14514
  199688. MAILLARD, B.
  199689. Can. J. Chem.C DISPLACEMENTS 
  199690. RADICALS 
  199691. ACCESS M
  199692. 15523N
  199693. 2/28/96
  199694. INTRAMOLECULAR HOMOLYTIC SUBSTITUTIONS.  INFLUENCE OF THE NATURE OF THE PEROXIDE FUNCTION ON INDUCED DECOMPOSITION OF d
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  199697. 1098Y
  199698. 14515
  199699. A    WOLFE, S.
  199700. Can. J. Chem.
  199701. LACTAM ANTIBIOTICS STREPTOMYCES
  199702. ALBUS
  199703. G SITE DIRECTED MUTAGENESIS ALLINGER MMP2(85) PROGRAM 
  199704. TRANSITION STATES 
  199705. CRYSTAL STRUCTURE 
  199706. ACTIVE SITE 
  199707. CATALYTIC MECHANISM BINDING PROTEINS ESCHERICHIA
  199708. COLI 
  199709. 15524N
  199710. 2/28/96
  199711. AG1992 LEMIEUX AWARD LECTURE 
  199712.  STUDIES RELATED to THE PENICILLIN RECEPTOR
  199713. 1994X    1014
  199714. 1032Y
  199715. 14516
  199716. CAMPI, E. M.
  199717. Aust. J. Chem.M
  199718. 15525N
  199719. 2/28/96
  199720. THE STEREOCHEMISTRY OF ORGANOMETALLIC COMPOUNDS .61. THE PREPARATION OF QUINAZOLINES and QUINAZOLINONES INVOLVING RHODIUM
  199721. CATALYSED HYDROFORMYLATION OF ALKENYL ANILINES
  199722. 1994X    1061
  199723. 1070Y
  199724. 14517
  199725. AnASTASIOU, D.
  199726. Aust. J. Chem.C<HYDROFORMYLATION 
  199727. PHASE 
  199728. CARBONYLATION 
  199729. DERIVATIVES 
  199730. OXIDES M
  199731. 15526N
  199732. 2/28/96
  199733. THE STEREOCHEMISTRY OF ORGANOMETALLIC COMPOUNDS .60. RHODIUM
  199734. CATALYSED REACTIONS OF HYDROGEN and CARBON MONOXIDE WITH ALKENYLANILINES
  199735. 1994X    1043
  199736. 1059Y
  199737. 14518
  199738. DYALL, L. K.
  199739. Aust. J. Chem.M
  199740. 15527N
  199741. 2/28/96
  199742. PYROLYSIS OF ARYL AZIDES .12. MECHANISTIC IMPLICATIONS OF THE VERY SMALL NEIGHBOURING GROUP EFFECTS ACROSS THE 2,3
  199743. BOND OF 2
  199744. AZIDONAPHTHALENE
  199745. 1994X    1031
  199746. 1042Y
  199747. 14519
  199748. BROWN, R. F. C.
  199749. Aust. J. Chem.C
  199750. ACID M
  199751. 15528N
  199752. 2/28/96
  199753. ALKYLATION and ELECTROPHILIC SUBSTITUTION REACTIONS OF 2
  199754. METHYLPYRAZOLO[1,5
  199755. A]PYRIDIN
  199756. OL and RELATED COMPOUNDS
  199757. 1994X    1009
  199758. 1021Y
  199759. 14520
  199760. BROWN, R. F. C.
  199761. Aust. J. Chem.M
  199762. 15529N
  199763. 2/28/96
  199764. A}THE PYROLYTIC REARRANGEMENT OF 1
  199765. ALKYNOYL
  199766. METHYLPYRAZOLES 
  199767.  SYNTHESIS OF PYRAZOLO[1,5
  199768. A]PYRIDIN
  199769. OLS and RELATED COMPOUNDS
  199770. 1994X
  199771. 1007Y
  199772. 14521
  199773. PASTO
  199774. Tet. Lett.CiRADICAL 
  199775. ALKOXY 
  199776. PHOTOCHEM 
  199777. CYCLIZATION 
  199778. FRAGMENTATION 
  199779. BENZENE 
  199780. SULFENATE 
  199781. THIO 
  199782. HYDROGEN 
  199783. ATOM TRANSFERM
  199784. 15530N
  199785. 2/28/96
  199786. DEMONSTRATION OF THE SYNTHETIC UTILITY OF THE GENERATION OF ALKOXY RADICALS BY HOMOLYTIC DISSOCIATION OF NITROBENZENE SULFENATES OF
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  199788. 14522
  199789. WEINREB
  199790. Tet. Lett.CEPI ALLYL PALLADIUM 
  199791. HECK 
  199792. TANDEM 
  199793. INTRAMOLECULAR 
  199794. CATALYST 
  199795. CARBANIONM
  199796. 15531N
  199797. 2/28/96
  199798. A_CONSECUTIVE CARBON
  199799. CARBON BOND FORMATION VIA THE p
  199800. ALLYL PALLADIUM VARIANT OF THE HECK REACTION
  199801. 1994X
  199802. 14523
  199803. MOTHERWELL
  199804. Tet. Lett.CQALKYNE 
  199805. RADICAL ADDITION CYCLIZATION 
  199806. VINYL TIN 
  199807. FLUORO 
  199808. SAMARIUM 
  199809. INTRAMOLECULARM
  199810. 15532N
  199811. 2/28/96
  199812. AYCOMPARATIVE STUDIES ON THE GENERATION and CYCLIZATION REACTIONS OF DIFLUOROALKYL RADICALS
  199813. 1994X
  199814. 14524
  199815. DoyleB
  199816. Tet. Lett.
  199817. AgRHODIUM 
  199818. DIAZO 
  199819. CHIRAL 
  199820. HYDROGEN 
  199821. H INSERTION 
  199822. ASYMMETRIC CATALYST LACTONE 
  199823. TRANSITION STATE 
  199824. WRITING
  199825. 15533N
  199826. 2/28/96
  199827. AxSYNTHESIS OF DEOXY XYLOLACTONE FROM GLYCEROL DERIVATIVES VIA HIGHLY ENANTIOSELECTIVE CARBON
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  199829. 1994X
  199830. 14525
  199831. QUAYLE
  199832. Tet. Lett.
  199833. AqBENZYNE 
  199834. FURAN 
  199835. INDOLE 
  199836. ALKALOID 
  199837. DIELS
  199838. ALDER CYCLOADDITION INTRAMOLECULAR 
  199839. REGIOCHEM 
  199840. SPECTROSCOPY 
  199841. WRITING
  199842. 15534N
  199843. 2/28/96
  199844. A.A NOVEL APPROACH to POLYCYCLIC INDOLIC SYSTEMS
  199845. 1994X
  199846. 14526
  199847. ROBERTSON 
  199848. Tet. Lett.CURADICAL REARRANGEMENT TIN 
  199849. ACYL SILANE 
  199850. ALKOXY 
  199851. BROOK 
  199852. SILYL 
  199853. NOVEL CARBONYL ADDITIONM
  199854. 15535N
  199855. 2/28/96
  199856. A\FREE RADICAL REARRANGEMENT OF ALKENYL EPOXY SILANES. ISOLATION OF A-TRIMETHYLSILYL ALDEHYDES
  199857. 1994X
  199858. 14527
  199859. Tet. Lett.C~DIAZO 
  199860. THIOIMIDE 
  199861. CARBENOID 
  199862. RHODIUM 
  199863. INTRAMOLECULAR CYCLIZATION ALKALOID 
  199864. SUPINIDINE 
  199865. SULFUR YLIDE 
  199866. THIOCARBONYL 
  199867. DANISHEFSKYM
  199868. 15536N
  199869. 2/28/96
  199870. AUA SYNTHESIS OF SUPINIDINE VIA AN INTRAMOLECULAR CARBENOID
  199871. THIOIMIDE COUPLING REACTION
  199872. 1994X
  199873. 14528
  199874. RIEKE
  199875. Tet. Lett.COTHIOPHENE 
  199876. LITHIO 
  199877. LITHIATION 
  199878. SUBSTITUTION 
  199879. ELECTRON 
  199880. METAL HALOGEN EXCHANGEM
  199881. 15537N
  199882. 2/28/96
  199883. A\ROOM TEMPERATURE STABLE 3
  199884. LITHIOTHIOPHENE. A FACILE SYNTHESIS OF 3
  199885. FUNCTIONALIZED THIOPHENES
  199886. 1994X
  199887. 14529
  199888. A    HEATHCOCK
  199889. Tet. Lett.CpAZOMETHINE YLIDE INTRAMOLECULAR DIPOLAR CYCLOADDITION CYCLOREVERSION
  199890. RETRO 
  199891. LAWESSON 
  199892. THIOAMIDE 
  199893. NOVEL MECHANISMM
  199894. 15538N
  199895. 2/28/96
  199896. AeUNUSUAL ISOMERIZATION UNDER LAWESSON THIATION CONDITIONS FROM AN AZOMETHINE YLIDE DERIVED CYCLOADDUCT
  199897. 1994X
  199898. 14530
  199899. JOCC@DIKETENE 
  199900. REVIEW 
  199901. REFERENCES 
  199902. ADDITIVE 
  199903. ALDRICH 
  199904. DICARBONYL
  199905.  LEADING REFERENCES SEE BACK OF VOL 59 J ORG CHEM
  199906. 15539N
  199907. 2/28/96V    DIKETENE W
  199908. 1994Y
  199909. 14531
  199910. A    RAPOPORT 
  199911. AFPROTECTION DEPROTECTION PROTECTING GROUP T
  199912. BOC SELECTIVE 
  199913. EXPERIMENTAL
  199914. 15540N
  199915. 2/28/96
  199916. AmSELECTIVE REMOVAL OF THE N
  199917. BOC PROTECTING GROUP IN THE PRESENCE OF A T
  199918. BUTYL ESTER and OTHER SENSITIVE GROUPS
  199919. 1994X
  199920. 3216Y
  199921. 14532
  199922. JOCCCAZIRIDINE RING OPENING REDUCTIVE CLEAVAGE RADICAL ANION NAPHTHALENEM
  199923. 15541N
  199924. 2/28/96
  199925. A5NAPHTHALENE CATALYZED REDUCTIVE OPENING OF AZIRIDINES
  199926. 1994X
  199927. 3210Y
  199928. 14533
  199929. NAJERA
  199930. JOCCMCARBANION 
  199931. VINYL 
  199932. LITHIATE 
  199933. EQUIVALENT 
  199934. UNSATURATED CARBOXYLIC ACID 
  199935. UMPOLUNGM
  199936. 15542N
  199937. 2/28/96
  199938. AJb-ACYL VINYL ANION EQUIVALENTS OF b-LITHIATED UNSATURATED CARBOXYLIC ACIDS
  199939. 1994X
  199940. 3202Y
  199941. 14534
  199942. COHEN 
  199943. JOCCUOXETANE RING OPENING THIOPHENYL CARBANION LITHIATE 
  199944. CRAM RULE 
  199945. SPIROKETAL 
  199946. STEREOCHEMM
  199947. 15543
  199948. 2/28/96
  199949. AHA GENERAL DIASTEREOSELECTIVE SYNTHESIS OF SPIROACETALS USING CERIUM IONS
  199950. 1994X
  199951. 3142Y
  199952. 14535
  199953. SONODA 
  199954. JACSC~ALCOHOL 
  199955. CARBON MONOXIDE CARBONYLATION 
  199956. LEAD TETRAACETATE 
  199957. ALKOXY RADICAL 
  199958. HYDROGEN ABSTRACTION ADDITION 
  199959. CYCLIZATION 
  199960. LACTONEM
  199961. 15544N
  199962. 2/28/96
  199963. A]REMOTE CARBONYLATION. THE SYNTHESIS OF g-LACTONES FROM SATURATED ALCOHOLS and CARBON MONOXIDE
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  199965. 5473Y
  199966. 14536
  199967. COMMINS 
  199968. AlDIHYDROPYRIDONES 
  199969. CHIRAL PYRIDINIUM ION ADDITION 
  199970. GRIGNARD 
  199971. HETEROCYCLIC 
  199972. ASYMMETRIC INDUCTION MM2 
  199973. ALKALOID
  199974. 15545N
  199975. 2/28/96
  199976. AjASYMMETRIC SYNTHESIS OF DIHYDRO
  199977. PYRIDONES BY ADDITION OF GRIGNARD REAGENTS to CHIRAL ACYL PYRIDINIUM SALTS
  199978. 1994X
  199979. 4719Y
  199980. 14537
  199981. BOLTON, R.
  199982. Tet. Lett.
  199983. AqA SIMPLE PROCEDURE FOR THE PREPARATION AND THE STEREOSELECTIVE REDUCTION OF SOME CAMPHOR BASED IMINES IS REPORTED
  199984. 15546N
  199985. 2/28/96
  199986. A0PREPARATION and REDUCTION OF SOME CAMPHOR IMINES
  199987. 1994X    3411
  199988. 3412Y
  199989. 14538
  199990. RAPOSO, C.
  199991. Tet. Lett.C
  199992. MOLECULAR RECOGNITION SOLVENTS
  199993. SEVERAL CARBOXYLATE GROUP RECEPTORS ABLE TO BIND SYN AND ANTI ELECTRON LONE PAIRS HAVE BEEN PREPARED MAKING USE OF AN AMINOCHROMENONE FRAGMENT. SYMMETRIC UREAS AND SULFURYL AMIDES PERMIT THE ESTABLISHMENT OF FOUR LINEAR HYDROGEN BONDS WITH THE CARBOXYLATE. THE FLAT GEOMETRY OF THE SULFURYL AMIDES COMPLEXES AND THE HIGHER ACIDITY OF THEIR HYDROGENS YIELD THE BEST ASSOCIATION CONSTANTS
  199994. 15547N
  199995. 2/28/96
  199996. A7READILY AVAILABLE CHROMENONE RECEPTORS FOR CARBOXYLATES
  199997. 1994X    3409
  199998. 3410Y
  199999. 14539
  200000. MUJICA, M. T.
  200001. Tet. Lett.C
  200002. ISOLAUREPINNACIN SYSTEMS 
  200003. A SYNTHETIC SEQUENCE FOR THE PREPARATION OF A,A'
  200004. DISUBSTITUTED CYCLIC ETHERS OF VARIOUS RING SIZES AND EITHER RELATIVE STEREOCHEMISTRY (CIS OR TRANS) IS PRESENTED. IT IS BASED ON THE HETERO DIELS-ALDER REACTION OF A MONOACTIVATED DIENE AND AN ALDEHYDE, YIELDING A SILYLENOL PYRONE WHICH IS TRANSFORMED INTO A LINEAR ETHER. THIS ETHER IS CYCLIZED BY AN INTRAMOLECULAR NUCLEOPHILIC SUBSTITUTION REACTION TO THE DESIRED CYCLIC ETHERS. THE VIABILITY OF THIS ROUTE IS DEMONSTRATED BY THE PREPARATIONB+ OF TWO EXAMPLES, AN OXOCANE AND AN OXOLANE
  200005. 15548N
  200006. 2/28/96
  200007. AWA VERSATILE APPROACH to CYCLIC ETHERS. SYNTHESIS OF DISUBSTITUTED OXEPANES and OXOCANES
  200008. 1994X    3401
  200009. 3404Y
  200010. 14540
  200011. A    RAUBO, P.
  200012. Tet. Lett.
  200013. ALLYLIC ALCOHOLS ASYMMETRIC EPOXIDATION EFFICIENT SYNTHESIS 
  200014. KINETIC RESOLUTION PRACTICAL METHOD 
  200015. SULFONYL ANIONS 
  200016. EPOXY ALCOHOLS A,B
  200017. EPOXYSILANES ALDEHYDES 
  200018. REAGENTS 
  200019. TRIMETHYLSILYL GLYCIDOL DERIVATIVES 1 WERE OXIDIZED WITH PYRIDINE N
  200020. OXIDES IN THE PRESENCE OF SILYLATING AGENTS TO GIVE THE CORRESPONDING GLYCERALDEHYDE DERIVATIVES 3. REACTION OF (A,b
  200021. EPOXYALLCYL)SILANES WITH N
  200022. OXIDES WAS STUDIED
  200023. 15549N
  200024. 2/28/96
  200025. OXIDATION OF AN A,b
  200026. (EPOXYALKYL)TRIMETHYLSILANE WITH PYRIDINE OXIDES IN THE PRESENCE OF SILYLATING AGENTS. A FACILE ENANTIOSELECTIVE SYNTHESIS OF GLYCERALDEHYDE DERIVATIVES
  200027. 1994X    3387
  200028. 3390Y
  200029. 14541
  200030. BONADIES, F.
  200031. Tet. Lett.C
  200032. TRIETHYLAMINE 
  200033. LITHIUM 
  200034. 3ALDEHYDES UNDERGO AN EFFICIENT E
  200035. STEREOSELECTIVE HORNER
  200036. WADSWORTH
  200037. EMMONS OLEFINATION BY GENERATION OF PHOSPHONATE CARBANION WITH LITHIUM HYDROXIDE. THE REACTION PROCEEDS SATISFACTORILY WITH LINEAR, CYCLIC, POLIFUNCTIONAL KETONES IN THE PRESENCE OF ACTIVATED ZEOLITES AND AND BY THE SLOW ADDITION OF THE BASE
  200038. 15550N
  200039. 2/28/96
  200040. AMA NEW PROCEDURE FOR HORNER
  200041. WADSWORTH
  200042. EMMONS OLEFINATION OF CARBONYL COMPOUNDS
  200043. 1994X    3383
  200044. 3386Y
  200045. 14542
  200046. A    CABRI, W.
  200047. Tet. Lett.
  200048. LACTAM ANTIBIOTICS EFFICIENT SYNTHESIS 
  200049. ACID 
  200050. HIGH YIELD ZINC HALIDES
  200051. MEDIATED REACTIONS BETWEEN THIOACID SALTS AND (3R,4R)4
  200052. ACETOXY
  200053. BUTYLDIMETHYLSILYLOXY)ETHYL]AZETIDIN
  200054. ONE IN NON PROTIC MEDIA ARE DESCRIBED
  200055. 15551N
  200056. 2/28/96
  200057. A{ZINC HALIDE
  200058. MEDIATED NUCLEOPHILIC ATTACK OF THIOACID SALTS IN NON PROTIC MEDIA. A KEY STEP IN THE TOTAL SYNTHESIS OF PENEMS
  200059. 1994X    3379
  200060. 3382Y
  200061. 14543
  200062. COSTANTINI, C.
  200063. Tet. Lett.
  200064. THE PHEOMELANIN PRECURSOR 1A AND THE RELATED DIHYDRO
  200065. BENZOTHIAZINES 1B
  200066. F UNDERGO RING CONTRACTION UPON IRRADIATION WITH PYREX
  200067. FILTERED UV LIGHT TO GIVE 2
  200068. METHYLBENZOTHIAZOLES 2A
  200069. F IN GOOD YIELDS
  200070. 15552N
  200071. 2/28/96
  200072. A<PHOTOCHEMICAL RING CONTRACTION OF DIHYDRO
  200073. BENZOTHIAZINES
  200074. 1994X    3365
  200075. 3366Y
  200076. 14544
  200077. ESTEVEZ, J. C.
  200078. Tet. Lett.CZCYCLOPENTANE 
  200079. AMINO ACIDS 
  200080. RING CONTRACTION HOMOCHIRAL TETRAHYDROFURANS LACTONES 
  200081. ANALOGS 
  200082. [BOTH d
  200083.  AND g
  200084. HEXONOLACTONES PROVIDE TEMPLATES FOR THE CONSTRUCTION OF BICYCLIC LACTONES IN WHICH A NEW TETRAHYDROPYRAN RING HAS BEEN FORMED FROM OVERALL ELIMINATION OF WATER FROM THE C
  200085. 2 AND C
  200086. 6 HYDROXYL GROUPS. SUCH STUDIES MAY PROVIDE A STRATEGY FOR THE SYNTHESIS OF C
  200087. GLYCOSIDES FROM ELIMINATION OF WATER BETWEEN C
  200088. 2 AND C
  200089. 6 OF HEPTONOLACTONES
  200090. 15553N
  200091. 2/28/96
  200092. A8TETRAHYDROPYRAN DERIVATIVES FROM g
  200093.  and d
  200094. HEXONOLACTONES
  200095. 1994X    3361
  200096. 3364Y
  200097. 14545
  200098. PAUSLER, G. M.
  200099. Tet. Lett.
  200100. FRIDAMYCIN E, DERIVATIVES OF ENT
  200101. FRIDAMYCIN E AND ENANTIOPURE INTERMEDIATES FOR VINEOMYCINS HAVE BEEN SYNTHESISED USING A TITANIUM(IV)
  200102. MEDIATED ADDITION OF (L)
  200103. MENTHYL ACETATE TO ACETONYL
  200104. SUBSTITUTED ANTHRARUFIN ETHERS
  200105. 15554N
  200106. 2/28/96
  200107. AOTITANIUM MEDIATION OF ALDOL REACTIONS IN FRIDAMYCIN and VINEOMYCINONE SYNTHESES
  200108. 1994X    3345
  200109. 3348Y
  200110. 14546
  200111. A    BIJOY, P.
  200112. Tet. Lett.
  200113. AnA NOVEL SYNTHESIS OF DIBENZOBICYCLO[3.2.2]NONANE SYSTEMS IS DESCRIBED THROUGH A DOUBLE FRIEDEL
  200114. CRAFTS REACTION
  200115. 15555N
  200116. 2/28/96
  200117. AVA NOVEL DOUBLE FRIEDEL
  200118. CRAFTS REACTION:   A NEW ENTRY INTO BICYCLO[3.2.2]NONANE SYSTEM
  200119. 1994X    3341
  200120. 3344Y
  200121. 14547
  200122. HACHIYA, I.
  200123. Tet. Lett.
  200124. A$TRIFLUOROMETHANESULFONATE 
  200125. SC(OTF)3 
  200126. ZIN THE PRESENCE OF A CATALYTIC AMOUNT OF SCANDIUM(III) PERCHLORATE (SC(CLO4)3), 1
  200127. ACETYL
  200128. 2,3,5
  200129. BENZYL
  200130. RIBOFURANOSE REACTED WITH TRIMETHYLSILYLATED NUCLEOPHILES TO AFFORD THE CORRESPONDING A
  200131. RIBOFURANOSIDES IN HIGH YIELDS WITH GOOD SELECTIVITIES. THE CATALYST COULD BE RECOVERED AFTER THE REACTIONS WERE COMPLETED AND COULD BE REUSED
  200132. 15556N
  200133. 2/28/96
  200134. AaSCANDIUM(III) PERCHLORATE (SC(CLO4)3). A NOVEL CATALYST IN THE A
  200135.  and N
  200136. GLYCOSYLATION REACTIONS
  200137. 1994X    3319
  200138. 3320Y
  200139. 14548
  200140. A    AKAJI, K.
  200141. Tet. Lett.
  200142. A#solid PHASE PEPTIDE SYNTHESIS 
  200143. ]CIP (2
  200144. CHLORO
  200145. DIMETHYLIMIDAZOLIDIUM HEXAFLUOROPHOSPHATE) WAS AN EFFICIENT COUPLING AGENT FOR N
  200146. PROTECTED A
  200147. AMINOISOBUTYRIC ACID (AIB) IN THE PRESENCE OF AN ADDITIVE. THE REACTIVITY WAS ENHANCED MARKEDLY BY A CATALYTIC AMOUNT OF ADDITIVE IN THE ORDER OF HOAT SIMILAR TO HODHBT>DMAP>HOBT. THESE COUPLINGS OCCURRED WITHOUT DETECTABLE RACEMIZATION
  200148. 15557N
  200149. 2/28/96
  200150. A[EFFICIENT COUPLING OF A,A
  200151. DIMETHYL AMINO ACID USING A NEW CHLORO IMIDAZOLIDIUM REAGENT, CIP
  200152. 1994X    3315
  200153. 3318Y
  200154. 14549
  200155. A    FACHE, F.
  200156. Tet. Lett.C
  200157. ALUMINA 
  200158. THE SELECTIVE N
  200159. ALKYLATION OF AMIDES (CYCLIC OR ACYCLIC) UNDER HYDROGEN IS REPORTED USING ALDEHYDES OR KETONES AS ALKYLATING AGENTS AND PD/C/NA2SO4 AS CATALYST. GOOD ISOLATED YIELDS ARE OBTAINED (81% TO 98%)
  200160. 15558N
  200161. 2/28/96
  200162. AJEXTENSION OF THE ESCHWEILER
  200163. CLARKE PROCEDURE to THE N
  200164. ALKYLATION OF AMIDES
  200165. 1994X    3313
  200166. 3314Y
  200167. 14550
  200168. FELIX, C. P.
  200169. Tet. Lett.CCTRIFLUOROMETHYLTRIMETHYLSILANE 
  200170. AZIRINES 
  200171. STEREOSELECTIVE ADDITION 
  200172. AkTHE ORIGINAL USE OF CF3SIME3 ON A CARBON NITROGEN DOUBLE BOND IS DESCRIBED. AZIRINES PROVIDE (E)
  200173. AZIRIDINES
  200174. 15559N
  200175. 2/28/96
  200176. AMSTEREOSELECTIVE ADDITION OF CF3SIME3 ON AZIRINES. SYNTHESIS OF (E)
  200177. AZIRIDINES
  200178. 1994X    3303
  200179. 3304Y
  200180. 14551
  200181. MARIA, E. J.
  200182. Tet. Lett.
  200183. AN(S) SERINE 
  200184. RADICAL 
  200185. ZN/CU COUPLE ELECTROREDUCTION CONJUGATE ADDITION OLEFINS 
  200186. AN EFFICIENT THREE STEP SYNTHESIS OF THE (R)
  200187.  AND (S)
  200188. AMINO
  200189. IODO)PROPANOL DERIVATIVES 4 AND 7 FROM (S) SERINE IS PROPOSED. THEIR USE IN RADICAL REACTIONS IS ILLUSTRATED
  200190. 15560N
  200191. 2/28/96
  200192. CONVENIENT PREPARATION OF (R)
  200193.  and (S)
  200194. AMINO
  200195. IODO)PROPANOL DERIVATIVES FROM (S)
  200196. SERINE: APPLICATION IN RADICAL ADDITION REACTIONS
  200197. 1994X    3301
  200198. 3302Y
  200199. 14552
  200200. BRUCKNER, R.
  200201. Tet. Lett.C
  200202. KETENE IMINE THIOCARBONYL 
  200203. THE [SIC],D
  200204. UNSATURATED NITRILE 2 EQUILIBRATES AT ROOM TEMPERATURE WITH THE N
  200205. ALLYLKETENE IMINE 3. DEUTERIUM LABELING ESTABLISHED AN INTRAMOLECULAR REARRANGEMENT, AND THE SMALL INFLUENCE OF SOLVENT POLARITY ON THE RARE CONSTANTS IS IN ACCORDANCE WITH A CONCERTED [3,3]SIGMATROPIC SHIFT
  200206. 15561N
  200207. 2/28/96
  200208. AKHOMOALLYL CYANIDE and N
  200209. ALLYLKETENE IMINE;  A [3,3] SIGMATROPIC EQUILIBRIUM
  200210. 1994X    3281
  200211. 3284Y
  200212. 14553
  200213. OJEA, V.
  200214. Tet. Lett.C=ASYMMETRIC SYNTHESIS ESTERS 
  200215. PHOSPHONATES PHOSPHORUS ANALOGS 
  200216. HIGH DIASTEREOSELECTIVITY IN THE CONJUGATE ADDITION OF LITHIATED SCHOLLKOPF'S BISLACTIM ETHERS TO E
  200217.  AND Z
  200218. ENYLPHOSPHONATES WAS UTILIZED TO ACHIEVE A DIRECT ASYMMETRIC SYNTHESIS OF ALL FOUR DIASTEREOISOMERS OF 2
  200219. AMINO
  200220. METHYL
  200221.  PHOSPHONOBUTANOIC ACID, I.E. (+)
  200222. (2S, 3R)
  200223. 4A, (+)
  200224. (2S, 3S)
  200225. 4B AND THEIR CORRESPONDING ENANTIOMERS. THEIR RELATIVE CONFIGURATION WAS DEFINITIVELY ASSIGNED FROM AN NMR STUDY OF OXAPHOSPHINANE DERIVATIVES OF BOTH DIASTEREOISOMERS
  200226. 15562N
  200227. 2/28/96
  200228. ENANTIOSPECIFIC SYNTHESIS OF 2
  200229. AMINO
  200230. METHYL
  200231. PHOSPHONOBUTANOIC ACIDS VIA 1,4
  200232. ADDITION OF LITHIATED SCHOLLKOPF ANION to PROP
  200233. ENYLPHOSPHONATES
  200234. 1994X    3273
  200235. 3276Y
  200236. 14554
  200237. HADJIARAPOGLOU, L.
  200238. Tet. Lett.CQSTEREOSELECTIVE TOTAL SYNTHESIS 
  200239. CYCLOADDITIONS (+/
  200240. GYMNOMITROL (+/
  200241. SATIVENE 
  200242. THE CASCADE CYCLOADDITION OF 1
  200243. ALKOXYCYCLOHEXADIENOLATES 2 ONTO 2
  200244. CHLORO
  200245.  CYCLOPROPYLIDENEACETATE 4 YIELDS 2
  200246. ALKOXYTRICYCLO[3.2.1.0(2.7)]OCTANE
  200247. DIONES 8 UNDER ACID CATALYSIS. THE TRICYCLOOCTANONES 7 CAN BE FURTHER ELABORATED, E. G. BY WITTIG OLEFINATION AND REDUCTION OF THE CARBONYL GROUP, OR DEPROTONATION AT THE BRIDGEHEAD C
  200248. 7 WITH SUBSEQUENT ALKYLATION, ACYLATION OR ALDOL REACTION, BEFORE THEY ARE REARRANGED TO THE HIGHLY FUNCTIONALIZED BICYCLO[3.2.1]OCTANE DERIVATIVES 10, 11, 13,B7 AND 17, RESPECTIVELY. THE DIONES 8 CAN ALSO BE FURTHER
  200249. 15563N
  200250. 2/28/96
  200251. AyFACILE SYNTHESIS OF HIGHLY FUNCTIONALIZED BICYCLO[3.2.1]OCTANES AS POTENTIAL BUILDING BLOCKS FOR VARIOUS NATURAL PRODUCTS
  200252. 1994X    3269
  200253. 3272Y
  200254. 14555
  200255. BOURGIN, D.
  200256. Tet. Lett.C
  200257. REARRANGEMENT CYCLIZATION 
  200258. THE DERIVATIVES OF TRANS
  200259. BICYCLO[3.3.0]OCTANE 3 AND 6 HAVE BEEN OBTAINED THE BICYCLO[3.3.0]OCT
  200260. ENES, STERICALLY HINDERED AT THE EXO
  200261. SIDE, VIA PHOTOINDUCED [2+2]CYCLOADDITION OF 1 WITH ETHYLVINYL ETHER AND BY HYDROBORATION
  200262. OXIDATION OF 5D, RESPECTIVELY
  200263. 15564N
  200264. 2/28/96
  200265. A:STEREOSELECTIVITY IN REACTIONS OF BICYCLO[3.3.0]OCT
  200266. 1994X    3267
  200267. 3268Y
  200268. 14556
  200269. NELSON, T. D.
  200270. Tet. Lett.CvHIGHLY STEREOSELECTIVE SYNTHESIS 
  200271. COUPLING REACTION 1,1'
  200272. BINAPHTHYLS RESOLUTION 
  200273. MECHANISM 
  200274. COMPLEXES 
  200275. CATALYST 
  200276. ACID 
  200277. ApHEATING A DIASTEREOMERIC MIX OF (62:  38) CHIRAL BIARYLS WITH CU
  200278. ION RESULTED IN A (93:  7) MIX OF DIASTEREOMERS
  200279. 15565N
  200280. 2/28/96
  200281. THE ASYMMETRIC ULLMANN REACTION .3. APPLICATION OF A FIRST
  200282. ORDER ASYMMETRIC TRANSFORMATION to THE SYNTHESIS OF C
  200283. SYMMETRIC, CHIRAL, NON
  200284. RACEMIC BIARYLS
  200285. 1994X    3259
  200286. 3262Y
  200287. 14557
  200288. HOFFMAN, R. V.
  200289. Tet. Lett.C
  200290. VERSATILE AMIDOALKYLATION REAGENTS 
  200291. SULFONYLATED HYDROXAMIC ACIDS 
  200292. NITROGEN REARRANGEMENTS ARYLSULFONYLOXY AMINES CATIONIC CARBON NUCLEOPHILES N
  200293. (BENZOTRIAZOL
  200294. YL)ALKYL]AMIDES N
  200295. (ARYLSULFONOXY)AMINES LACTAMS 
  200296. ROUTE 
  200297. TRIFLYLOXY AMIDES UNDERGO IONIZATION IN REFLUXING ISOPROPANOL TO GIVE N
  200298. ACYLIMINIUM IONS WHICH CAN BE TRAPPED BY ADDITION OF ALLYLTRIMETHYLSILANE TO THE REACTION MIXTURE. ALTERNATIVELY THEY CAN BE CONVERTED TO N
  200299. (ISOPROPOXY)ALKYL AMIDES AND THEN BACK TO N
  200300. ACYLIMINIUM IONS UNDER A VARIETY OF CONDITIONS
  200301. 15566N
  200302. 2/28/96
  200303. A`GENERATION OF N
  200304. ACYL IMINIUM IONS FROM IONIZATION
  200305. REARRANGEMENT REACTIONS OF N
  200306. TRIFLYLOXY AMIDES
  200307. 1994X    3231
  200308. 3234Y
  200309. 14558
  200310. RANE, A. M.
  200311. Tet. Lett.C
  200312. KETONES 
  200313. VINYL AND ARYL HALIDES ARE EFFICIENTLY CONVERTED, UNDER PD CATALYSIS, WITH KSTIPS (1) TO THE CORRESPONDING SILYL SULFIDES (2, 3). THE NAPHTHYL DERIVATIVE WAS EASILY HYDROLYZED TO THE MERCAPTAN 4, OR ALKYLATED OR ALKENYLATED TO PROVIDE UNSYMMETRICAL SULFIDES (5, 6)
  200314. 15567N
  200315. 2/28/96
  200316. AaPOTASSIUM TRIISOPROPYLSILANETHIOLATE: VINYL and ARYL SULFIDES THROUGH PD
  200317. CATALYZED CROSS COUPLING
  200318. 1994X    3225
  200319. 3226Y
  200320. 14559
  200321. MIRANDA, E. I.
  200322. Tet. Lett.C/ORGANIC SULFUR CHEMISTRY DERIVATIVES 
  200323. EPOXIDES 
  200324. tTRIISOPROPYLSILANETHIOL (HSTIPS, 1), EASILY PREPARED IN 98% YIELD FROM H2S AND TIPSCL, IS EFFICIENTLY ALKYLATED IN A SELECTIVE MANNER WITH 1 
  200325.  AND 2 
  200326.  ALKYL HALIDES OR TOSYLATES THROUGH ITS POTASSIUM THIOLATE (2C) TO PROVIDE RSTIPS (3) IN EXCELLENT YIELDS. COMPOUND 3 PROVIDES A CONVENIENT SOURCE OF ALKANETHIOLS (4), UNSYMMETRICAL DIALKYL SULFIDES (5) AND THIOACETALS (6)
  200327. 15568N
  200328. 2/28/96
  200329. A\THIOLS, UNSYMMETRICAL SULFIDES and THIOACETALS FROM THE NEW REAGENT: TRIISOPROPYLSILANETHIOL
  200330. 1994X    3221
  200331. 3224Y
  200332. 14560
  200333. A    WEBER, B.
  200334. TetrahedronC
  200335. ORGANOMETALLIC REAGENTS DIALKYLZINC COMPOUNDS ASYMMETRIC INDUCTION CARBONYL COMPOUNDS ALDEHYDES 
  200336. KETONES 
  200337. BENZALDEHYDE 
  200338. AUXILIARIES 
  200339. DIETHYLZINC 
  200340. ALCOHOLS 
  200341. IN THE PRESENCE OF EQUIMOLAR AMOUNTS OF THE MG ALKOXIDE FROM A,A,A', A'
  200342. TETRAPHENYL
  200343. DIMETHYL
  200344. DIOXOLAN
  200345. DIMETHANOL (A TADDOL) PRIMARY GRIGNARD REAGENTS (ET, PR, BU, OCT, 3
  200346. BUTENYL) ADD TO CARBO
  200347.  AND HETEROAROMATIC METHYL KETONES IN THF AT 
  200348.  C TO GIVE TERTIARY ALCOHOLS OF ENANTIOMERIC EXCESSES REACHING VALUES ABOVE 98%. THE SCOPE AND LIMITATION OF THE METHOD ARE INVESTIGATED. THE REACTION, WHICH OCCURS IN A VIGOROUSLY STIRRED HETEROGENEOUS MIXTURE, GIVES BEST RESULTS IN THE AB*BSENCE OF STERIC HINDRANCE OF THE REACTING
  200349. 15569N
  200350. 2/28/96
  200351. HIGHLY ENANTIOSELECTIVE ADDITION OF PRIMARY ALKYL GRIGNARD REAGENTS to CARBOCYCLIC and HETEROCYCLIC ARYLKETONES IN THE PRESENCE OF MAGNESIUM TADDOLATE PREPARATIVE and MECHANISTIC ASPECTS
  200352. 1994X    6117
  200353. 6128Y
  200354. 14561
  200355. VA    Ye, M. C.B
  200356. Tetrahedron
  200357. ASYMMETRIC INDUCTION ENANTIOSELECTIVE ADDITION OF ALKYLLITHIUM REAGENTS TO ALDEHYDES 
  200358. POLAR APROTIC SOLVENTS x-RAY CRYSTAL STRUCTURE ASYMMETRIC SYNTHESIS DIETHYL ETHER TETRAHYDROFURAN AUTOINDUCTION CYCLODEXTRINS 
  200359. BUTYLLITHIUM 
  200360. ENANTIOSELECTIVE INDUCTION BY SOME CHIRAL LITHIUM ALKOXIDES IN THE ADDITION OF METHYLLITHIUM TO BENZALDEHYDE HAS BEEN EXAMINED. A DETAILED STUDY OF 2
  200361. SUBSTITUTED LITHIUM 1
  200362. PHENYL
  200363. DIMETHYLAMINO)ETHOXIDES IN THE ADDITION OF ACHIRAL ALKYLLITHIUM REAGENTS TO ALDEHYDES IN THF AND DIETHYL ETHER AT 
  200364.  C HAS BEEN CARRIED OUT. THE EE'S ARE GENERALLY HIGHER IN THE FORMER SOLVENT. THE CONFIGURATION OF THE NEWLY FORMED CHIRAL CENTER IS OPPOSITE TO THAT OF THE 1
  200365. CARBON OF THE ALKOXIDE AND INDB4EPENDENT OF THAT OF ITS 2
  200366. CARBON ATOM. THE EE OF THE
  200367. 15570N
  200368. 2/28/96
  200369. AcENANTIOSELECTIVE ADDITION OF ALKYLLITHIUM REAGENTS to ALDEHYDES INDUCED BY CHIRAL LITHIUM ALKOXIDES
  200370. 1994X    6109
  200371. 6116Y
  200372. 14562
  200373. ELWORTHY, T. R.
  200374. TetrahedronCrSYNTHETIC EQUIVALENTS AMINOORGANOLITHIUMS REAGENTS 
  200375. EXCHANGE TETRAHYDROFURAN FORMAMIDINES 
  200376. BUTYLLITHIUM 
  200377. NITROGEN 
  200378. LITHIO PYRROLIDINE, AS ITS N
  200379. BOC OR FORMAMIDINE DERIVATIVE, HAS BEEN GENERATED IN HIGH ENANTIOMERIC PURITY VIA SN
  200380. LI EXCHANGE OF THE ENANTIOMERICALLY ENRICHED (88
  200381. 95%) A
  200382. TRIBUTYLSTANNANE DERIVATIVE, 4. THE ALKYLATION OF THESE LITHIO CARBANIONS GAVE 2
  200383. METHYL PYRROLIDINES AS WELL AS PROVIDING A MEASURE OF THEIR CONFIGURATIONAL STABILITY. IT WAS FOUND THAT THE A
  200384. LITHIO FORMAMIDINES WERE CONFIGURATIONALLY MORE STABLE THAN THE T
  200385. BOC DERIVATIVES AND THIS IS ATTRIBUTED TO THE STRONGER O
  200386. LI BOB6ND WHICH WEAKENS THE ADJACENT C
  200387. LI BOND, THUS ALLOWING
  200388. 15571N
  200389. 2/28/96
  200390. AjTHE CONFIGURATIONAL STABILITY OF CHIRAL LITHIO A
  200391. AMINO CARBANIONS. THE EFFECT OF LI
  200392. O VS LI
  200393. N COMPLEXATION
  200394. 1994X    6089
  200395. 6096Y
  200396. 14563
  200397. GAWLEY, R. E.
  200398. Tetrahedron
  200399. AMINO ORGANOLITHIUMS A
  200400. AMINO CARBANIONS 2
  200401. LITHIOPIPERIDINE 2
  200402. LITHIOPYRROLIDINE CONFIGURATIONALLY STABLE CARBANIONS 
  200403. DIPOLE STABILIZED ANIONS LITHIOAMINE 
  200404. SYNTHETIC EQUIVALENTS NUCLEAR MAGNETIC RESONANCE 
  200405. SINGLE ELECTRON TRANSFER ENANTIOSELECTIVE SYNTHESIS 
  200406. THE SEARCH FOR CONFIGURATIONALLY STABLE A
  200407. AMINO CARBANIONS HAS LED TO AN INTERESTING OBSERVATION OF DIFFERING REACTIVITY OF DIASTEREOMERIC ORGANOLITHIUMS AND TO THE CHARACTERIZATION OF ARACEMIC 2
  200408. LITHIO
  200409. METHYLPIPERIDINE AND 2
  200410. LITHIO
  200411. METHYLPYRROLIDINE AS CONFIGURATIONALLY STABLE A
  200412. AMINOORGANOLITHIUMS. DETAILS FOR THE PREPARATION OF THESE AND RELATED A
  200413. LITHIOHETEROCYCLES, EVALUATION OF THEIR CHEMICAL AND CONFIGURATIONAL STABILITY, AND A PRELIMINARY EVALUATION OF THE STEREOSELECTIVITY OF B
  200414. THEIR REACTIONS WITH
  200415. 15572N
  200416. 2/28/96
  200417. ADSEARCH FOR CONFIGURATIONALLY STABLE, ARACEMIC A
  200418. AMINO ORGANOLITHIUMS
  200419. 1994X    6077
  200420. 6088Y
  200421. 14564
  200422. KATRITZKY, A. R.
  200423. Tetrahedron
  200424. AWVINYL ETHER 
  200425. BENZOTRIAZOLE 
  200426. LITHIATION 
  200427. CALCULATION PM3 MNDO EQUIVALENTS 
  200428. PARAMETERS 
  200429. VBENZOTRIAZOLE
  200430. ASSISTED B
  200431. DEPROTONATION OF (A
  200432. BENZOTRIAZOLYLVINYL) ETHERS OCCURS STEREOSELECTIVELY AT THE CIS POSITION AS SHOWN BY QUENCHING WITH A VARIETY OF ELECTROPHILES. SEMIEMPIRICAL CALCULATIONS OF THE LITHIATED ENOL ETHERS BY PM3 AND MNDO METHODS DISCLOSED A HIGHER STABILIZATION FOR THE CIS
  200433. ISOMERS OVER THE CORRESPONDING TRANS
  200434. ISOMERS
  200435. 15573N
  200436. 2/28/96
  200437. A3BENZOTRIAZOLE
  200438. ASSISTED b
  200439. LITHIATION OF VINYL ETHERS
  200440. 1994X    6005
  200441. 6016Y
  200442. 14565
  200443. BAILEY, W. F.
  200444. TetrahedronC
  200445. CONJUGATE ADDITION REACTIONS 
  200446. HALOGEN INTERCHANGE REACTION 
  200447. DOUBLE BOND INTERACTIONS EXCHANGE 
  200448. LITHIUM BICYCLO[2.2.1]HEPTANES 5
  200449. HEXEN
  200450. YLLITHIUM REARRANGEMENTS CONSTRUCTION 
  200451. MECHANISM 
  200452. A SERIES OF 5
  200453. HEXENYLLITHIUMS HAVING A PHENYL, TRIMETHYLSILYL, OR CYCLOPROPYL SUBSTITUENT AT THE TERMINAL C6 ALKENE CARBON HAVE BEEN PREPARED FROM THE CORRESPONDING IODIDES BY LITHIUM
  200454. IODINE EXCHANGE WITH T
  200455. BUTYLLITHIUM AT 
  200456.  C. ALTHOUGH 6
  200457. ALKYL
  200458. SUBSTITUTED 5
  200459. HEXENYLLITHIUMS DO NOT ISOMERIZE TO FIVE
  200460. MEMBERED RINGS UPON WARMING, TERMINALLY SUBSTITUTED 5
  200461. HEXENYLLITHIUMS BEARING A MODERATELY ACTIVATING PHENYL OR TRIMETHYLSILYL GROUP CLEANLY UNDERGO A TOTALLY REGIOSPECIFIC 5
  200462. EXO CYCLIZATIONB
  200463.  AT SUB
  200464. AMBIENT
  200465. 15574N
  200466. 2/28/96
  200467. AgANIONIC CYCLIZATION OF OLEFINIC ALKYLLITHIUMS: RING CLOSURE OF TERMINALLY SUBSTITUTED 5
  200468. HEXENYLLITHIUMS
  200469. ZX    5957
  200470. 5970Y
  200471. 14566
  200472. TOMOOKA, K.
  200473. TetrahedronCdSYNTHETIC UTILITY 
  200474. ORGANIC SYNTHESIS RECOGNITION 
  200475. INVERSION 
  200476. REAGENTS STEREOCHEMISTRY CONFIGURATION 
  200477. THE [1,2]
  200478. WITTIG REARRANGEMENTS OF ENANTIO
  200479. DEFINED A
  200480. BENZYLOXYPROPYLLITHIUM AND ITS (R)
  200481. METHYLBENZYLOXY ANALOGS, GENERATED FROM THE ENANTIO
  200482. ENRICHED STANNANES VIA SN / LI EXCHANGE, ARE SHOWN TO PROCEED PREDOMINANTLY WITH INVERSION OF CONFIGURATION AT THE LI
  200483. BEARING TERMINUS AND RETENTION OF CONFIGURATION AT THE MIGRATING CENTER, AND EXHIBIT A SIGNIFICANT LEVEL OF MUTUAL ENANTIOMER RECOGNITION IN THE RADICAL RECOMBINATION PROCESS
  200484. 15575N
  200485. 2/28/96
  200486. [1,2]
  200487. WITTIG REARRANGEMENT OF ENANTIO
  200488. DEFINED A
  200489. ALKOXYALKYLLITHIUMS: STRUCTURAL REQUIREMENT and STERIC COURSE AT THE LI
  200490. BEARING TERMINUS
  200491. 1994X    5927
  200492. 5932Y
  200493. 14567
  200494. MIKAMI, K.
  200495. TetrahedronC
  200496. STEROID SIDE CHAINS
  200497.  [2,3] WITTIG SIGMATROPIC REARRANGEMENT
  200498.  CARBOXYLIC ACID DERIVATIVES 
  200499. PROPARGYL ETHER SYSTEM STEREOCONTROLLED SYNTHESIS 
  200500. ACYCLIC STEREOCONTROL ERYTHRO
  200501. SELECTIVITY 
  200502. CHIRAL SYNTHESIS 
  200503. TRANSITION STRUCTURES OF [2,3]
  200504. WITTIG REARRANGEMENTS OF ALLYLOXYMETHYL ANION, ALLYLOXYPROPARGYL ANION, ALLYLOXYACETALDEHYDE ANION, AND THEIR 1
  200505. METHYL (CROTYL) AND 3
  200506. METHYL ANALOGS HAVE BEEN LOCATED. THE TRANSITION STRUCTURE OF THE REARRANGEMENT OF ALLYLOXYMETHYL ANION IS EXTREMELY EARLY, WITH THE C
  200507. C BOND NEARLY UNFORMED, AND LARGELY REFLECTS INVERSION OF THE CARBANION CENTER AND BREAKING OF C3
  200508. O4 BOND. THE TRANSITION STRUCTURE BECOMES MUCH DIFFERENT WHEN THE ANION IS STABILIZED BY AN ETHYB
  200509. NYL SUBSTITUENT;  N
  200510. 15576N
  200511. 2/28/96
  200512. DIFFERENT TRANSITION STRUCTURES FOR [2,3]
  200513. WITTIG REARRANGEMENTS OF STABILIZED and UNSTABILIZED ALLYLOXY METHYL ANIONS: RATIONALE FOR THE DICHOTOMOUS SENSE OF STEREOSELECTION
  200514. 1994X    5917
  200515. 5926Y
  200516. 14568
  200517. A    BOCHE, G.
  200518. Tetrahedron
  200519. ELECTRON CORRELATION ENERGY 
  200520. ORGANIC SYNTHESIS PERTURBATION THEORY TRIMETHYLSILYLDIAZOMETHANE REAGENTS 
  200521. SYNTHON
  200522. ISOMERS 
  200523. ISOTHIOCYANATES 
  200524. AMINATION 
  200525. CH2N2 
  200526. THE FIRST REPORT OF A METALATED DIAZOMETHANE BY EUGEN MULLER AND HIS COWORKERS APPEARED IN 1933. THEN, IN A THIRTY
  200527. SIX YEARS ONGOING STORY, 1
  200528. 6 THIS GROUP REVEALED HIGHLY INTERESTING BUT ALSO PUZZLING DETAILS ABOUT THE CHEMISTRY OF METALATED DIAZOMETHANE AND METALATED SUBSTITUTED DIAZOMETHANES:   1. METALATION OF DIAZOMETHANE 1A (THE PARENT COMPOUND) TO GIVE THE CORRESPONDING LI (OR NA) SPECIES FOLLOWED BY PROTONATION LED TO ''ISODIAZOMETHANE'' WHICH FINALLY TURNED OUT TO BE N
  200529. ISOCYANO AMIB
  200530. NE 1C. 
  200531. 15577N
  200532. 2/28/96
  200533. LITHIO
  200534. DIAZOMETHANE AND LITHIO
  200535. (TRIMETHYLSILYL)DIAZOMETHANE: THEORETICAL and EXPERIMENTAL STUDIES OF THEIR STRUCTURES, REACTIONS and REACTION PRODUCTS
  200536. 1994X    5889
  200537. 5902Y
  200538. 14569
  200539. REICH, H. J.
  200540. Tetrahedron
  200541. LOW TEMPERATURE 
  200542. C13 NMR 
  200543. ORGANOLITHIUM COMPOUNDS HEXAMETHYLPHOSPHORIC TRIAMIDE 
  200544. CRYSTAL STRUCTURE 
  200545. CARBONYL COMPOUNDS A
  200546. ENONES 
  200547. DITHIANES 
  200548. SULFUR CARBANIONS 
  200549. >AN NMR STUDY OF 2
  200550. LITHIO
  200551. DITHIANE AND 2
  200552. TRIORGANOSILYL
  200553. BUTYL
  200554.  AND 2
  200555. PHENYL
  200556. LITHIODITHIANES REVEALS THAT ALL ARE CONTACT ION PAIR SPECIES IN THF AND ALL BECOME SEPARATED IONS WITH EXCESS HMPA. THE DITHIANES DIFFER GREATLY IN THEIR EASE OF ION SEPARATION, WITH THE PARENT LITHIODITHIANE THE MOST DIFFICULT
  200557. 15578N
  200558. 2/28/96
  200559. AISOLUTION ION PAIR STRUCTURE OF 2
  200560. LITHIO
  200561. DITHIANES IN THF and THF
  200562. 1994X    5869
  200563. 5880Y
  200564. 14570
  200565. A    KNORR, R.
  200566. TetrahedronC
  200567. AGGREGATION 
  200568. CRYSTAL STRUCTURE 
  200569. LITHIATION 
  200570. ORGANOLITHIUM COMPOUNDS 
  200571. REACTIVITY 
  200572. STERICALLY CONGESTED MOLECULES 
  200573. ORGANOLITHIUM COMPOUNDS 
  200574. x-RAY CRYSTAL STRUCTURE INDUCED CHEMICAL SHIFTS COUPLING CONSTANTS 
  200575. CRYSTALLINE 2
  200576. (LITHIOMETHYLENE)
  200577. 1,1,3,3
  200578. TETRAMETHYLINDAN (3) FORMS THE ETHERATE 11 AS A CENTROSYMMETRIC DIMER WITH A LICLIC FOUR
  200579. MEMBERED RING. THE CARBANIONIC TERMINAL OF EACH OF THE TWO CC DOUBLE BONDS IS TETRACOORDINATED, BEING BONDED AT ALMOST EQUAL DISTANCES TO THE TWO LITHIUM CATIONS ABOVE AND BELOW THE PLANE CONTAINING BOTH THE DOUBLE BOND AND THE VINYLIC HYDROGEN ATOM. FOR EACH LITHIUM CATION, TETRACOORDINATION IS ACHIEVED BY BONDING TO TWO CARBANION CENTERS, TO THE OXYGEN ATOM OF B=ONE ETHER MOLECULE, AND (WEAKLY) TO ONE OF THE METHYL GROUPS.
  200580. 15579N
  200581. 2/28/96
  200582. A b,b
  200583. SHIELDED VINYLLITHIUM EXAMPLE FOR A QUANTIFICATION OF STRUCTURE, MONOMER
  200584. DIMER EQUILIBRIUM, and SOME REACTIVITY PARAMETERS
  200585. 1994X    5845
  200586. 5860Y
  200587. 14571
  200588. HIRAKI, K.
  200589. OrganometallicsC
  200590. PLATINUM 
  200591. METALS 
  200592. CRYSTAL STRUCTURE CATALYZED 
  200593. ISOMERIZATION 
  200594. SIMPLE ENOLS 
  200595. COMPLEXES 
  200596. RUTHENIUM 
  200597. MECHANISM 
  200598. DERIVATIVES 
  200599. IRIDIUM 
  200600. OSMIUM M
  200601. 15580N
  200602. 2/28/96
  200603. A}REACTIONS OF RUCLH(CO)(PPH3)3 WITH ALLYLIC AMINES 
  200604.  INSERTIONS and AN UNUSUAL CARBON NITROGEN BOND CLEAVAGE OF ALLYLIC AMINES
  200605. 1994X    1878
  200606. 1885Y
  200607. 14572
  200608. Liu, C. H.B
  200609. OrganometallicsCxSIGMATROPIC REARRANGEMENTS 
  200610. ACYCLIC 1,5
  200611. DIENES ORGANIC HALIDES NORBORNADIENE COMPLEXES 
  200612. INSERTION 
  200613. NORTRICYCLENES 
  200614. BOND M
  200615. 15581N
  200616. 2/28/96
  200617. AqPALLADIUM
  200618. CATALYZED ADDITION OF ALKYNE to NORBORNENE DERIVATIVES 
  200619.  UNUSUAL RING FORMATION and EXPANSION REACTIONS
  200620. 1994X    1832
  200621. 1839Y
  200622. 14573
  200623. Yeh, M. C. P.B
  200624. OrganometallicsC^ORGANOIRON REAGENTS ORGANIC SYNTHESIS COMPLEXES 
  200625. REACTIVITY 
  200626. CONSTRUCTION ORGANOCOPPER 
  200627. ENONESM
  200628. 15582N
  200629. 2/28/96
  200630. MICHAEL ADDITION REACTIONS OF THE HIGHLY FUNCTIONALIZED ZINC COPPER REAGENTS RCU(CN)ZNI to (TROPONE)IRON TRICARBONYL PROMOTED BY BORON TRIFLUORIDE ETHERATE
  200631. 1994X    1788
  200632. 1794Y
  200633. 14574
  200634. MITZEL, N. W.
  200635. OrganometallicsC
  200636. ELECTRON DIFFRACTION DETERMINATION 
  200637. MOLECULAR STRUCTURES 
  200638. GAS PHASE 
  200639. SILYLAMINES 
  200640. CHEMISTRY 
  200641. SILICON 
  200642. SILYL DERIVATIVES 
  200643. CRYSTAL 
  200644. BOND M
  200645. 15583N
  200646. 2/28/96
  200647. ABSILYLHYDROXYLAMINES 
  200648.  COMPOUNDS WITH UNUSUAL NITROGEN COORDINATION
  200649. 1994X    1762
  200650. 1766Y
  200651. 14575
  200652. PEARSON, A. J.
  200653. OrganometallicsC<CYCLIZATION 
  200654. ENYNES 
  200655. BICYCLIZATION 
  200656. COMPLEXES 
  200657. ALKYNE 
  200658. ACID M
  200659. 15584N
  200660. 2/28/96
  200661. A;CYCLOCARBONYLATION OF 1,6
  200662. ENYNES PROMOTED BY IRON CARBONYLS
  200663. 1994X    1656
  200664. 1661Y
  200665. 14576
  200666. ZHOU, J. Q.
  200667. OrganometallicsCmCARBON MONOXIDE SILYLFORMYLATION HYDROFORMYLATION HYDROSILANE 
  200668. COBALT 
  200669. HYDROSILYLATION 
  200670. DERIVATIVES 
  200671. OLEFINS M
  200672. 15585N
  200673. 2/28/96
  200674. AWZWITTERIONIC RHODIUM(I) COMPLEX CATALYZED NET SILYLHYDROFORMYLATION OF TERMINAL ALKYNES
  200675. 1994X    1586
  200676. 1591Y
  200677. 14577
  200678. BOCELLI, G.
  200679. J.C.S. Perkin Trans. 1CtCONTAINING CYCLIC AMIDE HYDROGEN TRANSFER COMPLEXES 
  200680. ACIDS 
  200681. MECHANISM 
  200682. OXIDATION 
  200683. ALCOHOLS 
  200684. CRYSTAL 
  200685. LIGANDS 
  200686. ESTER M
  200687. 15586N
  200688. 2/28/96
  200689. AxCONTROL OF REGIOSELECTIVITY BY CHELATING SUBSTRATES IN SOME RHODIUM(I) and RHODIUM(III)
  200690. CATALYSED REACTIONS OF BUTADIENE
  200691. 1994X    1347
  200692. 1357Z
  200693. 14578
  200694. A    SELVA, M.
  200695. J.C.S. Perkin Trans. 1C/PHASE
  200696. TRANSFER CATALYSIS OXIDATIVE DECYANATION M
  200697. 15587N
  200698. 2/28/96
  200699. A]SELECTIVE MONO
  200700. METHYLATION OF ARYLACETONITRILES and METHYL ARYLACETATES BY DIMETHYL CARBONATE
  200701. 1994X    1323
  200702. 1328Z
  200703. 14579
  200704. CROMBIE, L.
  200705. J.C.S. Perkin Trans. 1M
  200706. 15588N
  200707. 2/28/96
  200708. STEREOCHEMISTRY OF THERMOLYTIC BASE
  200709. CATALYSED DECARBOXYLATION to FORM CONJUGATED DIENE
  200710. ACIDS: SYNTHESIS USING ETHYLIDENEMALONIC ESTER CONDENSATION
  200711. 1994X    1267
  200712. 1274Z
  200713. 14580
  200714. Soai, K.B
  200715. J.C.S. Perkin Trans. 1CtD
  200716. THREO
  200717. SPHINGOSINE STEREOSELECTIVE SYNTHESIS L
  200718. SERINE 
  200719. ORGANOMETALLIC REAGENTS ACID DERIVATIVES 
  200720. PRODUCTS
  200721. IN VITRO M
  200722. 15589N
  200723. 2/28/96
  200724. ASYMMETRIC ALKENYLATION OF CHIRAL AND PROCHIRAL ALDEHYDES CATALYSED BY CHIRAL OR ACHIRAL AMINO ALCOHOLS: CATALYTIC DIASTEREOSELECTIVE SYNTHESIS OF PROTECTED ERYTHRO
  200725. SPHINGOSINE and ENANTIOSELECTIVE SYNTHESIS OF CHIRAL DIALLYL ALCOHOLS
  200726. 1994X    1257
  200727. 1258Z
  200728. 14581
  200729. ELSAYED, I.
  200730. J.C.S. Perkin Trans. 1M
  200731. 15590N
  200732. 2/28/96
  200733. CHLOROTROPIC REARRANGEMENTS OF AN A
  200734. SULFANYL
  200735. SULFONYLALKANESULFENYL CHLORIDE to AN A
  200736. CHLOROALKYL DISULFIDE and AN S
  200737. CHLOROALKYL) THIOSULFONATE
  200738. 1994X    1251
  200739. 1252Z
  200740. 14582
  200741. BALCERZAK, P.
  200742. J. Chem. Res.
  200743. PHASE M
  200744. 15591N
  200745. 2/28/96
  200746. A SIMPLE SYNTHESIS OF GEM
  200747. DIFLUOROCYCLOPROPANES FROM BROMOFORM DIBROMODIFLUOROMETHANE IN A BASIC PHASE TRANSFER CATALYTIC SYSTEM
  200748. 1994X
  200749. 14583
  200750. Wang, M. X.B
  200751. J. Chem. Res.
  200752. 15592N
  200753. 2/28/96
  200754. AASPECTRAL and STRUCTURAL PROPERTIES OF HETEROCYCLIC KETENE ANIMALS
  200755. 1994X
  200756. 14584
  200757. MEERPOEL, L.
  200758. NONCONJUGATED CHROMOPHORES 
  200759. DOUBLE BOND 
  200760. DEFORMATION 
  200761. ELECTRONIC CONTROL CYCLOADDITIONS STEREOCHEMICAL COURSE CYCLOPENTADIENE RINGS ORGANIC ELECTROPHILES BICYCLIC FRAMEWORKS ORGANOTIN REAGENTS COUPLING CONSTANTsM
  200762. 15593N
  200763. 2/28/96
  200764. FACE SELECTIVITY OF THE DIELS
  200765. ALDER ADDITIONS and CHELETROPIC ADDITIONS OF SULFUR DIOXIDE to 2
  200766. VINYL
  200767. OXABICYCLO[2.2.1]HEPT
  200768. ENE DERIVATIVES
  200769. 14585
  200770. WESSIG, P.
  200771. Helv. Chim. Acta
  200772. AMINO ACIDS PHOTOCHEMISTRY AMINOKETONES 
  200773. PYRROLIDINE
  200774. 15594N
  200775. 2/28/96
  200776. A_ASYMMETRIC SYNTHESIS OF 3
  200777. HYDROXYPROLINES BY PHOTOCYCLIZATION OF N
  200778. BENZOYLETHYL)GLYCINAMIDES
  200779. 1994X
  200780. 14586
  200781. Koch, T.B
  200782. Helv. Chim. ActaC
  200783. ETHERS M
  200784. 15595N
  200785. 2/28/96
  200786. ADMACROCYCLIC IMIDES: VERSATILE SYNTHONS IN RING
  200787. ENLARGEMENT REACTIONS
  200788. 1994X
  200789. 14587
  200790. MULLER, P.
  200791. Helv. Chim. ActaC
  200792. METAL CARBENE TRANSFORMATIONS ASYMMETRIC SYNTHESIS 
  200793. H INSERTION CYCLOPROPANATION REACTIONS 
  200794. CARBOXYLATES 
  200795. OLEFINS 
  200796. ESTERS 
  200797. CARBOXAMIDES 
  200798. COMPLEXES 
  200799. LIGANDS M
  200800. 15596N
  200801. 2/28/96
  200802. AjENANTIOSELECTIVE FORMATION OF BICYCLIC LACTONES BY RHODIUM
  200803. CATALYZED INTRAMOLECULAR CH
  200804. INSERTION REACTIONS
  200805. 1994X
  200806. 14588
  200807. WALTER, H.
  200808. Helv. Chim. ActaM
  200809. 15597N
  200810. 2/28/96
  200811. ADA NOVEL APPROACH to 2,2
  200812. DISUBSTITUTED 1,2
  200813. DIHYDRO
  200814. PHENYLQUINOLINES
  200815. 1994X
  200816. 14589
  200817. PERROCHEAU, J.
  200818. Bull. Soc. Chim. Belg.
  200819. rC-1,3
  200820. DIPOLAR CYCLOADDITIONS 
  200821. NITROGEN 
  200822. ESTERS M
  200823. 15598N
  200824. 2/28/96
  200825. A8REACTION OF O
  200826. SUBSTITUTED OXIMES WITH 2-AZOMETHINE YLIDS
  200827. 1994X
  200828. 14590
  200829. GUIBOURDENCHE, C.
  200830. Bull. Soc. Chim. Belg.
  200831. KAINIC ACID 
  200832. TURN MIMETICS 
  200833. 15599N
  200834. 2/28/96
  200835. A/AMINOACIDS, PEPTIDES and HETEROCYCLIC CHEMISTRY
  200836. 1994X
  200837. 14591
  200838. SCHILBACH, W.
  200839. Angew. Chem. Int. Ed. Engl. M
  200840. 15600N
  200841. 2/28/96
  200842. A0REACTIONS OF AN IMINOPHOSPHORANYLIDENE CARBENOID
  200843. 1994X
  200844. 14592
  200845. TIETZE, L. F.
  200846. Angew. Chem. Int. Ed. Engl. M
  200847. 15601N
  200848. 2/28/96
  200849. ASYMMETRIC 1,6
  200850. INDUCTION IN HETERO
  200851. DIELS
  200852. ALDER REACTIONS OF CHIRAL OXABUTADIENES FOR A DE NOVO SYNTHESIS OF ENANTIOMERICALLY PURE CARBOHYDRATES:   LEWIS ACID DEPENDENT REVERSAL OF FACIAL SELECTIVITY
  200853. 1994X
  200854. 14593
  200855. WESSJOHANN, L.
  200856. Angew. Chem. Int. Ed. Engl. M
  200857. 15602N
  200858. 2/28/96
  200859. A"THE FIRST TOTAL SYNTHESES OF TAXOL
  200860. 1994X
  200861. 14594
  200862. A    GRIGG, R.
  200863. Tet. Lett.C
  200864. CYCLOPENTENONES 
  200865. PD(0), GENERATED IN
  200866. SITU, IN COMBINATION WITH TIOAC PROMOTES A RANGE OF CATALYTIC BI
  200867.  AND TRI
  200868. MOLECULAR CYCLOADDITIONS OF ARYL/HETEROARYL IODIDES IN WHICH CARBON MONOXIDE (1 ATM) FUNCTIONS AS A ONE CARBON COMPONENT FURNISHING 5 
  200869.  7 MEMBERED RINGS IN GOOD YIELD
  200870. 15603N
  200871. 2/28/96
  200872. AXCARBON MONOXIDE AS A ONE CARBON COMPONENT IN PALLADIUM CATALYSED CYCLOADDITION REACTIONS
  200873. 1994X    3197
  200874. 3200Y
  200875. 14595
  200876. Malm, J.B
  200877. Tet. Lett.
  200878. DERIVATIVES OF BENZO[C]
  200879. NAPHTHYRIDINE HAVE BEEN PREPARED IN FAIR TO EXCELLENT YIELDS AND IN ONE STEP BY THE PD(0)
  200880. CATALYZED CROSS
  200881. COUPLING OF PYRIDINE METHYLSTANNANES WITH ORTHO BROMOACETANILIDES. THE COUPLING IS GREATLY PROMOTED BY THE ADDITION OF COPPER(II)OXIDE
  200882. 15604N
  200883. 2/28/96
  200884. SYNTHESIS OF BENZO[C]
  200885. NAPHTHYRIDINES BY PALLADIUM
  200886. CATALYZED COUPLING OF PYRIDINE METHYLSTANNANES WITH ORTHO-BROMOACETANILIDES IN THE PRESENCE OF COPPER(II) OXIDE
  200887. 1994X    3195
  200888. 3196Y
  200889. 14596
  200890. CIAPETTI, P.
  200891. Tet. Lett.
  200892. 1 PROTEASE INHIBITOR PEPTIDE BOND ISOSTERES SOLID
  200893. PHASE SYNTHESIS DIPEPTIDE ISOSTERES STEREOSELECTIVE SYNTHESIS RENIN INHIBITORS 
  200894. TRANSITION STATE CONVENIENT 
  200895. ANALOG 
  200896. DIFFERENTLY SUBSTITUTED ALLYLIC BROMIDES REACT WITH N
  200897. PROTECTED AMINO ALDEHYDES TO GIVE INTERMEDIATE PRODUCTS FOR THE SYNTHESIS OF HYDROXYETHYLENE DIPEPTIDE ISOSTERES. THE LOW STEREOSELECTIVITY OF THIS REACTION CAN BE IMPROVED USING ALDEHYDES PROTECTED WITH HINDERED GROUPS. THIS REACTION CAN BE EFFICIENTLY APPLIED TO OLIGOPETIDE ALDEHYDES. WE DESCRIBE A PROTOCOL, FOR THE PREPARATION OF PEPTIDES CONTAINING AN HYDROXYETHYLENE ISOSTERE, WHICH ALLOWS A RAPID VARIATIONS OF THE AMINOACID SEQUENCB
  200898. 15605N
  200899. 2/28/96
  200900. CRCL2 MEDIATED ALLYLATION OF N
  200901. PROTECTED A
  200902. AMINO ALDEHYDES. A VERSATILE SYNTHESIS OF POLYPEPTIDES CONTAINING AN HYDROXYETHYLENE ISOSTERE
  200903. 1994X    3183
  200904. 3186Y
  200905. 14597
  200906. Cox, G. G.B
  200907. Tet. Lett.C
  200908. CATALYZED REACTIONS 
  200909. RHODIUM(ii) CARBOXYLATE CATALYSED DECOMPOSITION OF DIAZO ESTERS 3 AND 4 IN THE PRESENCE OF ALCOHOLS OR WATER RESULTS INFORMATION OF 2
  200910. ALKOXY
  200911.  OR 2
  200912. HYDROXY
  200913. ARYLPROPANOATES RESPECTIVELY BY O
  200914. H INSERTION IN COMPETITION WITH CINNAMATES BY ELIMINATION;  THE RATIO OF INSERTION TO ELIMINATION IS DRAMATICALLY AFFECTED BY THE CARBOXYLATE LIGAND ON RHODIUM. USE OF METHANOL
  200915. D AS THE ALCOHOL CONFIRMS THAT THE ALKENE DOES NOT ARISE BY ELIMINATION FROM THE INITIAL ALKOXYESTER PRODUCT
  200916. 15606N
  200917. 2/28/96
  200918. ArCOMPETING O
  200919. H INSERTION and b
  200920. ELIMINATION IN RHODIUM CARBENOID REACTIONS;  SYNTHESIS OF 2
  200921. ALKOXY
  200922. ARYLPROPANOATES
  200923. 1994X    3139
  200924. 3142Y
  200925. 14598
  200926. A    ISEKI, K.
  200927. Tet. Lett.C
  200928. REDUCTION 
  200929. THE TRIFLUOROMETHYLATION OF ALDEHYDES AND KETONES WITH TRIFLUOROMETHYLTRIMETHYLSILANE CATALYZED BY CHIRAL QUARTERNARY AMMMONIUM FLUORIDES WAS CARRIED OUT ENANTIOSELECTIVELY TO GIVE OPTICALLY ACTIVE 1
  200930. SUBSTITUTED
  200931. 2,2,2
  200932. TRIFLUOROETHANOLS
  200933. 15607N
  200934. 2/28/96
  200935. ASYMMETRIC TRIFLUOROMETHYLATION OF ALDEHYDES and KETONES WITH TRIFLUOROMETHYL TRIMETHYSILANE CATALYZED BY CHIRAL QUATERNARY AMMONIUM FLUORIDES
  200936. 1994X    3137
  200937. 3138Y
  200938. 14599
  200939. MIKAMI, K.
  200940. Tet. Lett.
  200941. HIGH ENANTIOMERIC PURITIES a
  200942. HYDROXY ESTERS 
  200943. ORGANIC SYNTHESIS O
  200944. METHYLMANDELATE PRACTICAL ACCESS 
  200945. ETHERS 
  200946. ALLYLSILANES 
  200947. ALLYLATION 
  200948. ALDEHYDES 
  200949. ALCOHOLS
  200950. THE CHIRAL LEWIS ACID PREPARED FROM (R)
  200951. BINAPHTHOL AND DIISOPROPOXYTITANIUM DICHLORIDE CATALYZES THE REACTION OF GLYOXYLATE ESTERS WITH METHALLYLSILANES TO AFFORD MAINLY ENE
  200952. TYPE PRODUCTS RATHER THAN THE PRODUCTS EXPECTED FROM THE ''USUAL'' SAKURAI
  200953. HOSOMI REACTION. THE ENE
  200954. TYPE PRODUCTS LEAD EVENTUALLY AFTER PROTODESILYLATION TO THE ''USUAL'' PRODUCTS WITH HIGH ENANTIOMERIC EXCESSES
  200955. 15608N
  200956. 2/28/96
  200957. ENE APPROACH to ASYMMETRIC CATALYSIS OF THE ''SAKURAI
  200958. HOSOMI REACTION'', LEWIS ACID
  200959. PROMOTED CARBONYL
  200960. ADDITION REACTION WITH ALLYLIC SILANES
  200961. 1994X    3133
  200962. 3136Y
  200963. 14600
  200964. SUGIYAMA, J.
  200965. Tet. Lett.C,CIS
  200966. DIVINYL EPOXIDES COPE REARRANGEMENT 
  200967. STYRYL OR 2
  200968. VINYL SUBSTITUTED 4
  200969. METHYLENE
  200970. DIOXOLANES UNDERWENT THE CLAISEN REARRANGEMENT TO OBTAIN 4,5
  200971. DIHYDRO
  200972. 3(2H)
  200973. OXEPINONES IN GOOD YIELD. THE RATE OF REACTION FOLLOWED THE DECREASING ORDER:   2
  200974. PHENYL
  200975. STYRYL > 2
  200976. PHENYL
  200977. VINYL > 2
  200978. BUTYL
  200979. STYRYL > 2
  200980. STYRYL
  200981. 15609N
  200982. 2/28/96
  200983. AvRING EXPANSION REACTION OF 2
  200984. VINYL
  200985. METHYLENE-1,3
  200986. DIOXOLANES to 4,5
  200987. DIHYDRO
  200988. 3(2H)
  200989. OXEPINONES BY CLAISEN REARRANGEMENT
  200990. 1994X    3111
  200991. 3114Y
  200992. 14601
  200993. Kato, K.B
  200994. Tet. Lett.
  200995. (S,S)
  200996. CYCLOHEXANE
  200997. DIOL (S,S)
  200998. CYCLOHEPTANE
  200999. DIOL 
  201000. ASYMMETRIC OXIDATION
  201001. ASYMMETRIC EPOXiDATION CHIRAL AUXILIARY
  201002. CHIRAL ENOL ESTER 
  201003. POXIDATION OF CHIRAL B'
  201004. TRIMETHYLSILYLOXY ENOL ETHERS 2A
  201005. D AND B'
  201006. HYDROXY ENOL ETHERS 3A
  201007. E, PREPARED FROM THE CORRESPONDING B
  201008. KETO ESTERS, WITH MCPBA AFFORDED a
  201009. HYDROXY ESTERS (4A
  201010. D AND 5A
  201011. E) IN A HIGHLY DIASTEREOSELECTIVE MANNER. THE ABSOLUTE CONFIGURATIONS OF THE NEWLY GENERATED STEREOGENIC CENTER IN 4 AND 5 WERE FOUND TO BE CONTRARY
  201012. 15610N
  201013. 2/28/96
  201014. A?ASYMMETRIC OXIDATION OF b
  201015. KETO ESTERS USING CHIRAL CYCLIC DIOLS
  201016. 1994X    3103
  201017. 3104Y
  201018. 14602
  201019. A    MONTI, H.
  201020. Tet. Lett.C[TRIMETHYLSILYLCYCLOPENTANE ANNULATION STEREOSELECTIVE SYNTHESIS ALLYLSILANES 
  201021. SPECTROSCOPY 
  201022. =NMR EXPERIMENTS UNEQUIVOCALLY SHOW THAT THE BY
  201023. PRODUCT OBTAINED FROM THE ZNI2
  201024. PROMOTED REACTION OF AN ALLYLTRIMETHYLSILANE WITH 3
  201025. BUTYN
  201026. ONE IS A [2+2] CYCLOADDITION COMPOUND. THIS FACT CORROBORATES OUR PREVIOUSLY DESCRIBED ASSIGNMENT. IN THE EXPERIMENTAL CONDITIONS USED, THE REACTION OCCURS WITHOUT 1,3
  201027. SILYL SHIFT
  201028. 15611N
  201029. 2/28/96
  201030. ZNI2 CATALYSED [2+2] VERSUS [3+2] CYCLOADDITION OF AN ALLYLTRIMETHYLSILANE WITH 3
  201031. BUTYN
  201032. ONE:   CONFIRMATION OF A CYCLOBUTENE BY
  201033. PRODUCT FORMATION
  201034. 1994X    3073
  201035. 3076Y
  201036. 14603
  201037. CAHIEZ, G.
  201038. Tet. Lett.
  201039. ENOLATES ARE READILY CONVERTED TO MN
  201040. ENOLATES BY TREATMENT WITH MANGANESE HALIDES. IN THF, THE REACTION IS EASILY AND ECONOMICALLY PERFORMED WITH MANGANESE CHLORIDE AT ROOM TEMPERATURE. MN
  201041. ENOLATES CAN THEN BE REGIOSELECTIVELY MONOALKYLATED IN GOOD YIELDS. THE FORMATION OF DI-  AND POLYALKYLATED PRODUCTS IS NEVER OBSERVED (< 1%)
  201042. 15612N
  201043. 2/28/96
  201044. AeHIGHLY REGIOSELECTIVE MONOALKYLATION OF KETONES VIA MANGANESE ENOLATES PREPARED FROM LITHIUM ENOLATES
  201045. 1994X    3069
  201046. 3072Y
  201047. 14604
  201048. JEFFERY, T.
  201049. Tet. Lett.C
  201050. PALLADIUM CATALYZED VINYLATION 
  201051. PHASE
  201052. TRANSFER CATALYSIS COUPLING REACTIONS ORGANIC HALIDES 
  201053. AQUEOUS MEDIA 
  201054. ARYL HALIDES 
  201055. SUBSTITUTION 
  201056. ACID 
  201057. kTHE PRESENCE OF WATER IS DETERMINING FOR THE EFFICIENCY OF QUATERNARY AMMONIUM SALT (QX) IN PALLADIUM
  201058. CATALYSED VINYLATION OF ORGANIC HALIDES USING AN ALKALI METAL CARBONATE AS THE BASE, WHETHER QX IS A CHLORIDE, A BROMIDE OR A HYDROGENSULFATE. THE [PD/M2CO3/QX] CATALYST SYSTEM CAN EVEN BE USED FOR PERFORMING THE REACTIONS IN NEAT WATER, WITHOUT ORGANIC SOLVENT
  201059. 15613N
  201060. 2/28/96
  201061. TYPE REACTIONS IN WATER
  201062. 1994X    3051
  201063. 3054Y
  201064. 14605
  201065. CASARA, P.
  201066. Tet. Lett.C!ACID 
  201067. AMINOTRANSFERASE INHIBITOR 
  201068. SUCCESSIVE THERMAL REACTIONS BASED ON A CLAISEN AND AN OVERMAN REARRANGEMENT FURNISH AN ORIGINAL ACCESS TO VIGABATRIN STARTING FROM ERYTHRITOL
  201069. 15614N
  201070. 2/28/96
  201071. A.VIGABATRIN SYNTHESIS BY THERMAL REARRANGEMENTS
  201072. 1994X    3049
  201073. 3050Y
  201074. 14606
  201075. NAMBIAR, K. P.
  201076. Tet. Lett.C
  201077. DERIVATIVES 
  201078. REMOVAL 
  201079. A MILD METHOD FOR SELECTIVE CLEAVAGE OF TETRAHYDROPYRANYL ETHERS IN THE PRESENCE OF OTHER ACID SENSITIVE FUNCTIONALITIES SUCH AS ACETONIDES, METHOXYMETHYL ETHERS, METHYLENEDIOXY ETHERS, MESITALDEHYDE ACETALS AND T
  201080. BUTYLDIMETHYLSILYL ETHERS USING LEWIS ACID
  201081. THIOL SYSTEM IS DESCRIBED
  201082. 15615N
  201083. 2/28/96
  201084. AuA MILD METHOD FOR SELECTIVE CLEAVAGE OF TETRAHYDROPYRANYL ETHERS IN THE PRESENCE OF OTHER ACID
  201085. LABILE FUNCTIONALITIES
  201086. 1994X    3033
  201087. 3036Y
  201088. 14607
  201089. Guan, X. M.B
  201090. Tet. Lett.C7INDOLE
  201091. ACETIC ACIDS INDOLE
  201092. GLYOXYLIC ACIDS ANALOGS 
  201093. SCHINZER, D.
  201094. SynlettC
  201095. HETEROCYCLES 
  201096. ACIDS M
  201097. 15617N
  201098. 2/28/96
  201099. BECKMANN REARRANGEMENTS/ALLYLSILANE CYCLIZATIONS 
  201100.  APPROACH to THE PENTACYCLIC CEPHALOTAXINE
  201101. FRAMEWORK and THE INFLUENCE OF THE TERMINATING SILICON GROUP
  201102. A>A CONVENIENT METHOD FOR THE SYNTHESIS OF INDOLE
  201103. ACETIC ACIDS
  201104. 1994X    3013
  201105. 3016Y
  201106. 14608
  201107. SCHINZER, D.
  201108. SynlettC
  201109. HETEROCYCLES 
  201110. ACIDS M
  201111. 15617N
  201112. 2/28/96
  201113. BECKMANN REARRANGEMENTS/ALLYLSILANE CYCLIZATIONS 
  201114.  APPROACH to THE PENTACYCLIC CEPHALOTAXINE
  201115. FRAMEWORK and THE INFLUENCE OF THE TERMINATING SILICON GROUP
  201116. 1994X
  201117. 14609
  201118. ZAHOUILY, M.
  201119. Synlett
  201120. SULFINYL RADICALS ADDITION REACTIONS SUBSTITUTED RADICALS STEREOSELECTIVITY 
  201121. ACIDS 
  201122. 15618N
  201123. 2/28/96
  201124. AwGOOD to EXCELLENT DIASTEREOSELECTIVITIES IN ASYMMETRIC RADICAL CYCLIZATIONS OF OPTICALLY PURE b
  201125. ALKOXY VINYL SULFOXIDES
  201126. 1994X
  201127. 14610
  201128. A    CHINO, M.
  201129. SynlettC|PALLADIUM CATALYZED HYDROSTANNATION 
  201130. ORGANIC SYNTHESIS REAGENT 
  201131. TRANSMETALATION HYDROCARBONS 
  201132. COMPLEXES 
  201133. ALDEHYDES 
  201134. OLEFINS M
  201135. 15619N
  201136. 2/28/96
  201137. AkCONVENIENT PROCEDURE FOR SELECTIVE GENERATION OF ALLYLZIRCONOCENE CHLORIDES VIA HYDROZIRCONATION OF ALLENES
  201138. 1994X
  201139. 14611
  201140. SASAKI, H.
  201141. Synlett
  201142. ADACTIVE (SALEN)MANGANESE(III) COMPLEXES ENANTIOSELECTIVE EPOXIDATION 
  201143. 15620N
  201144. 2/28/96
  201145. AgCONSTRUCTION OF HIGHLY EFFICIENT MN
  201146. SALEN CATALYST FOR ASYMMETRIC EPOXIDATION OF CONJUGATED CIS
  201147. OLEFINS
  201148. 1994X
  201149. 14612
  201150. HASHIMOTO, S.
  201151. Synlett
  201152. AGHOMOCHIRAL RHODIUM(II) CARBOXYLATES 
  201153. ASYMMETRIC SYNTHESIS CARBOXAMIDES 
  201154. 15621N
  201155. 2/28/96
  201156. ENANTIOSELECTIVE INTRAMOLECULAR C
  201157. H INSERTION REACTIONS OF A
  201158. DIAZO-b
  201159. KETO ESTERS CATALYZED BY DIRHODIUM(II) TETRAKIS[N
  201160. PHTHALOYL
  201161. PHENYLALANINATE] 
  201162.  THE EFFECT OF THE SUBSTITUENT AT THE INSERTION SITE ON ENANTIOSELECTIVITY
  201163. 1994X
  201164. 14613
  201165. QUESNELLE, C. A.
  201166. SNIECKUS, V. 
  201167. SynlettC
  201168. CARBON BOND FORMATION GRIGNARD REAGENTS POLYSUBSTITUTED AROMATICS UNSYMMETRICAL BIARYLS SYNTHETIC REACTIONS EFFICIENT ROUTE 
  201169. PALLADIUM 
  201170. HALIDES 
  201171. TRANSFORMATIONS HALOARENES 
  201172. ZINC 
  201173. ORTHO METALATION 
  201174. ARYL TRIFLATE 
  201175. CROSS COUPLING 
  201176. 15622N
  201177. 2/28/96
  201178. DIRECTED ORTHO
  201179. METALATION 
  201180.  CROSS COUPLING CONNECTIONS 
  201181.  NICKEL(0)
  201182. CATALYZED CROSS COUPLING OF ARYL TRIFLATES WITH ORGANOZINC REAGENTS
  201183. 1994X
  201184. 14614
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  201714. H BOND:   NORBORNENYLIDENES
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  201721. NITRONE CYCLOADDITIONS M
  201722. 15665N
  201723. 2/28/96
  201724. UNPRECEDENTED REARRANGEMENT OF 5
  201725. BENZOYL SUBSTITUTED BICYCLIC ISOXAZOLIDINES to DEHYDROPYRROLIZIDIN
  201726. ONES and INDOLIZIDIN
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  201733. 2/28/96
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  201740. JACSM
  201741. 15667N
  201742. 2/28/96
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  201751. 2/28/96
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  201760. 2/28/96
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  201769. 15670N
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  201784. x-RAY CRYSTAL
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  201790. 2/28/96
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  201801. SELENIUM BOND 1,2
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  201830. PALLADIUM COMPLEXES CYCLIZATION 
  201831. 15674N
  201832. 2/28/96
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  201864. 2/28/96
  201865. AzENANTIOSELECTIVE PREPARATION OF 1,3
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  201880. 15678N
  201881. 2/28/96
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  201893. AITHERMOLYSIS OF ARYL AZIDOMETHYL KETONE N
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  201903. CHIRAL SOLVATING AGENTS ABSOLUTE CONFIGURATION ENANTIOMERIC PURITY OPTICAL ISOMERS 
  201904. OLEFINS 
  201905. RESOLUTION 
  201906. LACTONESM
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  201908. 2/28/96
  201909. A.ENANTIOSELECTIVE AMINOHYDROXYLATION OF ALKENES
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  201925. 2/28/96
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  201946. 2/28/96
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  201975. CYCLIC SULFONES 
  201976. LITHIATION REAGENTS 
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  201983. 61% YIELDS
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  202030. 2/28/96
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  202062. PARTNER
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  202077. CATALYSED REACTION OF VINYL HALIDES WITH THE ANIONS OF 1,1
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  202080. DIENYL G
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  202087. ASPALLADIUM
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  202089. BUTADIANYLMALONATES TO g
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  202113. INTERCHANGE 
  202114. CHEMISTRY 
  202115. RAPID METAL
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  202123. INITIATED SEQUENTIAL CONJUGATE ADDITION REACTIONS
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  202131. 15695N
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  202133. A)PREPARATION AND USE OF 1
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  202141. AxAN N
  202142.  VS. O
  202143. ALKYLATION STUDY OF 2
  202144. PYRIDONE WITH VARIOUS ALCOHOLS AND SOLVENTS UNDER MITSUNOBU CONDITIONS WAS CARRIED OUT
  202145. 15696N
  202146. 2/28/96
  202147.  VS O
  202148. ALKYLATION IN THE MITSUNOBU REACTION OF 2
  202149. PYRIDONE
  202150. 1994X    2819
  202151. 2822Y
  202152. 14688
  202153. NAJERA, C.
  202154. Tetrahedron
  202155. AHDIELS
  202156. ALDER REACTION REAGENT 
  202157. CHEMISTRY 
  202158. SULFONES 
  202159. SYSTEM 
  202160. ROUTE 
  202161. ACIDS 
  202162. THE ALKYLATION OF THE MONOLITHIUM DERIVED 5 OF 2
  202163. (CHLOROMETHYL)
  202164. TOSYLPROPENE (1) WITH BROMO
  202165.  OR IODO
  202166. METHYLTRIMETHYLSILANE AFFORDS THE B
  202167. SILYL SULFONE 7, WHICH AFTER NUCLEOPHILIC SUBSTITUTION OF THE CHLORINE ATOM FOLLOWED BY B
  202168. ELIMINATION OF TOSYLTRIMETHYLSILANE, PROMOTED BY TETRABUTYLAMMONIUM FLUORIDE (TBAF), GIVES 2
  202169. SUBSTITUTED CONJUGATED DIENES 6 AND THE OUTER
  202170. RING DIENE 14. RACEMIC IPSENOL (10B), AN AGGREGATION PHEROMONE OF THE BARK BEETLE IPS PARACONFUSUS LANIER, IS PREPARED
  202171. 15697N
  202172. 2/28/96
  202173. ArA GENERAL METHOD FOR THE SYNTHESIS OF 2
  202174. ALKYL SUBSTITUTED 1,3
  202175. DIENES STARTING FROM 2
  202176. (CHLOROMETHYL)
  202177. TOSYLPROPENE
  202178. 1994X    5829
  202179. 5844Y
  202180. 14689
  202181. ANNUNZIATA, R.
  202182. Tetrahedron
  202183. ADDITION OF TRICTHYLAMINE TO A MIXTURE OF 2
  202184. PYRIDYLTHIOESTERS AND SNCL4 OR SNBR4 AFFORDS THE CORRESPONDING TIN(IV) ENOLATES THAT ADD TO IMINES TO GIVE B
  202185. LACTAMS IN FAIR TO GOOD YIELDS AND WITH VARIOUS DEGREE OF TRANS/CIS STEREOSELECTIVITY. EXAMPLES OF HIGHLY DIASTEREOFACIALLY SELECTIVE REACTIONS CARRIED OUT ON A CHIRAL THIOESTER AND ON A CHIRAL IMINE ARE ALSO REPORTED. THE RESULTS ARE COMPARED WITH THOSE OBTAINED IN THE CONDENSATIONS PROMOTED BY TICL4 AND TIBR4
  202186. 15698N
  202187. 2/28/96
  202188. SYNTHESIS OF b
  202189. LACTAMS BY CONDENSATION OF THE TIN ENOLATES OF 2
  202190. PYRIDYLTHIOESTERS WITH IMINES. A COMPARISON BETWEEN TITANIUM AND TIN ENOLATES
  202191. 1994 X    5821
  202192. 5828Y
  202193. 14690
  202194. A    TAKAO, K.
  202195. Tetrahedron
  202196. INTRAMOLECULAR N
  202197. ALKYLATION OF D
  202198. GLUCOSE
  202199. DERIVED SUBSTRATE 21E PROCEEDED IN AN SN2' MODE SMOOTHLY IN THE PRESENCE OF A PD(O) CATALYST AND N
  202200. BU4NI. THE MAJOR CYCLIZATION PRODUCT, A 2,6
  202201. DIALKYLATED PIPERIDINE 22T, WAS EFFECTIVELY CONVERTED INTO THE TITLE ALKALOIDS
  202202. 15699N
  202203. 2/28/96
  202204. STEREOSELECTIVE TOTAL SYNTHESES OF (
  202205. DESOXOPROSOPININE AND (
  202206. DESOXOPROSOPHYLLINE:   PALLADIUM(O)
  202207. CATALYZED INTRAMOLECULAR N
  202208. ALKYLATION FOR THE KEY PIPERIDINE RING FORMATION
  202209. 1994X    5681
  202210. 5704Y
  202211. 14691
  202212. Baba, Y.B
  202213. TetrahedronC
  202214. EURYFURAN 
  202215. FURAN 
  202216. RING TRANSFER REACTION [3,3]SIGMATROPIC REARRANGEMENT 
  202217. ROBINSON ANNULATION DRIMANE
  202218. RELATED SESQUITERPENES 
  202219. EFFICIENT SYNTHESIS 
  202220. iTWO EFFECTIVE SYNTHETIC APPROACHES TO (+/
  202221. EURYFURAN 1 ARE DESCRIBED. ONE SYNTHETIC ROUTE MAKES USE OF SEQUENTIAL FURAN RING TRANSFER REACTION TYPE I AND TYPE III AS KEY STEPS FOLLOWED BY ESCHENMOSER
  202222. TYPE [3,3]SIGMATROPIC REARRANGEMENT, AND ANOTHER ROUTE PROCEEDED THROUGH FURAN RING TRANSFER REACTION TYPE I AND ANNULATION WITH ETHYL VINYL KETONE SUBSEQUENTLY
  202223. 15700N
  202224. 2/28/96
  202225. AXALTERNATIVE SYNTHETIC APPROACHES TO (+/
  202226. EURYFURAN VIA THE FURAN RING TRANSFER REACTION
  202227. 1994X    5645
  202228. 5658Y
  202229. 14692
  202230. AMPUTCH, M. A.
  202231. Tetrahedron
  202232. AeCONJUGATE ADDITION REACTIONS 
  202233. DIELS
  202234. ALDER REACTIONS NUCLEOPHILIC ADDITION ACRYLATES 
  202235. CAMPHOR 
  202236. ESTERS 
  202237. THE MICHAEL INITIATED RING CLOSURE REACTION HAS BEEN EXPLORED WITH AN EYE TOWARD ACHIEVING ASYMMETRIC INDUCTION. THE FORMATION OF THREE, FIVE AND SIX
  202238. MEMBERED RINGS WAS EXAMINED USING COMPOUNDS 1
  202239. 7 AS SUBSTRATES. IN THE CASE OF CYCLOPROPANE FORMATION, DIASTEREOSELECTIVITY WAS STUDIED OVER A RANGE OF TEMPERATURES, THE BEST RESULTS BEING OBTAINED BETWEEN 
  202240. 68 AND 
  202241.  C USING LITHIUM 1
  202242. BUTHYLTHIOLATE AS THE NUCLEOPHILE AND A 10
  202243. DICYCLOHEXYLSULFAMOYL
  202244. ISOBORNEOL
  202245. DERIVED AUXILIARY (72
  202246. 78% YIEB/LD, 50
  202247. 56% DE;  NOTE EQUATION 5). AN ISOKINETIC
  202248. 15701N
  202249. 2/28/96
  202250. ACASYMMETRIC INDUCTION IN THE MICHAEL INITIATED RING CLOSURE REACTION
  202251. 1994X    5591
  202252. 5614Y
  202253. 14693
  202254. EDWARDS, M. L.
  202255. TetrahedronC6ESTERIFICATION REACTION AMINES 
  202256. SULFONAMIDES 
  202257. ANALOGS K
  202258. THE MITSUNOBU REACTION HAS BEEN USED IN THE SYNTHESIS OF POLYAMINE ANALOGUES. THE SYNTHESIS OF THE (R,R), (S,S) AND MESO
  202259.  ISOMERS OF A TETRAAMINE ARE DESCRIBED. THE CHEMISTRY WAS USED TO SYNTHESIZE A FLUORINATED POLYAMINE ANALOG AND A HEXAAMINEM
  202260. 15702N
  202261. 2/28/96
  202262. A<USE OF THE MITSUNOBU REACTION IN THE SYNTHESIS OF POLYAMINES
  202263. 1994X    5579
  202264. 5590Y
  202265. 14694
  202266. GASSMAN, P. G.
  202267. Syn. Commun.C
  202268. VINYL RADICAL CYCLIZATION M
  202269. 15703N
  202270. 2/28/96
  202271. AOTANDEM CYCLIZATION OF b
  202272. DICARBONYL ENOL
  202273. PHOSPHATES BY ELECTROCHEMICAL REDUCTION
  202274. 1994X    1465
  202275. 1474Y
  202276. 14695
  202277. GASSMAN, P. G.
  202278. Syn. Commun.
  202279. A DIELS
  202280. ALDER REACTIONS CATALYSIS 
  202281. 15704N
  202282. 2/28/96
  202283. APVINYLCYCLOPROPANE REARRANGEMENT OF ETHYL 6
  202284. ETHENYLBICYCLO[3.1.0]HEXANE
  202285. ACETATE
  202286. 1994X    1457
  202287. 1463Y
  202288. 14696
  202289. MATSUMOTO, M.
  202290. Syn. Commun.
  202291. SEMMLER
  202292. WOLFF AROMATIZATION 
  202293. 15705N
  202294. 2/28/96
  202295. AQPALLADIUM
  202296. CATALYZED DEHYDRATIVE AROMATIZATION OF CYCLOHEXENONE OXIMES TO ANILINES
  202297. 1994X    1441
  202298. 1446Y
  202299. 14697
  202300. VILLEMIN, D.
  202301. Syn. Commun.C
  202302. DITHIOACETALS 
  202303. ALUMINA M
  202304. 15706N
  202305. 2/28/96
  202306. A CONVENIENT SYNTHESIS OF CYCLOPROPANES FROM OLEFIN AND CARBON ACID COMPOUNDS 
  202307.  SYNTHESIS OF TETRAETHYL CYCLOPROPANEDIYLDIPHOSPHONATES
  202308. 1994X    1425
  202309. 1431Y
  202310. 14698
  202311. LESKOVSEK, V.
  202312. Syn. Commun.M
  202313. 15707N
  202314. 2/28/96
  202315. A;A NEW APPROACH TO THE SYNTHESIS OF N
  202316. ARYLAKYL AMINOALCOHOLS
  202317. 1994X    1415
  202318. 1424Y
  202319. 14699
  202320. MUELLERWESTERHOFF, U. T.
  202321. Syn. Commun.C
  202322. PYRROLE M
  202323. 15708N
  202324. 2/28/96
  202325. ArAZINES AND IMINES OF 4
  202326. PYRROLE
  202327. ALDEHYDE AND 5
  202328. PYRROLE
  202329. ALDEHYDE 
  202330.  A USEFUL SYNTHESIS OF THE ALDEHYDES
  202331. 1994X    1389
  202332. 1393Y
  202333. 14700
  202334. WALLBAUM, S.
  202335. Syn. Commun.ClENANTIOSELECTIVE ADDITION ASYMMETRIC SYNTHESES REDUCTIONS 
  202336. ALDEHYDES 
  202337. INDUCTION 
  202338. CATALYST 
  202339. ANALOGS 
  202340. KETONES M
  202341. 15709N
  202342. 2/28/96
  202343. DECARBOXYLATION OF A
  202344. AMINO ACIDS CONTAINING two AND three STEREOGENIC CENTERS 
  202345.  A SIMPLE ONE
  202346. STEP PROCEDURE TO PREPARE two OPTICALLY ACTIVE b
  202347. AMINO ALCOHOLS AND A BICYCLIC PYRROLIDINE DERIVATIVE
  202348. 1994X    1381
  202349. 1387Y
  202350. 14701
  202351. Gray, M. A.B
  202352. Syn. Commun.C
  202353. AGENT M
  202354. 15710N
  202355. 2/28/96
  202356. A/FUNCTIONALISATION OF 2
  202357. METHOXY
  202358. METHYLPYRIDINE
  202359. 1994X    1367
  202360. 1379Y
  202361. 14702
  202362. A    RONNE, E.
  202363. Syn. Commun.C
  202364. HETEROCYCLIC AMINES M
  202365. 15711N
  202366. 2/28/96
  202367. A=ONE
  202368. STEP SYNTHESIS OF 2
  202369. AMINO
  202370. METHYLIMIDAZO[4,5
  202371. B]QUINOLINE
  202372. 1994X    1363
  202373. 1366Y
  202374. 14703
  202375. TICKNER, A. M.
  202376. Syn. Commun.M
  202377. 15712N
  202378. 2/28/96
  202379. A2AN EFFICIENT SYNTHESIS OF CATECHOL CYCLIC SULFATES
  202380. 1994X    1631
  202381. 1637Y
  202382. 14704
  202383. A    TOSTE, D.
  202384. Syn. Commun.C
  202385. BENZOSTABASE M
  202386. 15713N
  202387. 2/28/96
  202388. AhFORMAMIDINE AS A VERSATILE PROTECTING GROUP FOR PRIMARY AMINES 
  202389.  A MILD PROCEDURE FOR HYDROLYTIC REMOVAL
  202390. 1994X    1617
  202391. 1624Y
  202392. 14705
  202393. KRYSAN, D. J.
  202394. Syn. Commun.M
  202395. 15714N
  202396. 2/28/96
  202397. AeAN EXPEDIENT ROUTE TO ENANTIOPURE (Z)
  202398. ALLYLIC ALCOHOLS VIA A
  202399. HYDROXY ACID
  202400. DERIVED 1,3
  202401. DIOXOLAN
  202402. 1994X    1589
  202403. 1596Y
  202404. 14706
  202405. A    Yu, H. S.B
  202406. Syn. Commun.M
  202407. 15715N
  202408. 2/28/96
  202409. A1UNSATURATED LACTONES 
  202410.  SYNTHESIS AND APPLICATIONS
  202411. 1994X    1583
  202412. 1588Y
  202413. 14707
  202414. JURSIC, B. S.
  202415. Syn. Commun.M
  202416. 15716N
  202417. 2/28/96
  202418. AjPREPARATION OF 5
  202419. SUBSTITUTED 2
  202420. METHYL
  202421. 1,3,4
  202422. OXADIAZOLES FROM 5
  202423. SUBSTITUTED TETRAZOLES AND ACETIC ANHYDRIDE
  202424. 1994X    1575
  202425. 1582Y
  202426. 14708
  202427. GRIDNEV, A. A.
  202428. Syn. Commun.M
  202429. 15717
  202430. 2/28/96
  202431. SYNTHESIS OF 1
  202432. ALKYLIMIDAZOLES
  202433. 1994X    1547
  202434. 1555Y
  202435. 14709
  202436. FISHER, G. B.
  202437. Syn. Commun.CjREMARKABLY SIMPLE SYNTHESIS 
  202438. CORRESPONDING ALKENES CONVENIENT CONVERSION HYDROBORATION 
  202439. ALCOHOLS 
  202440. KETONES M
  202441. 15718N
  202442. 2/28/96
  202443. AIA FACILE NEW SYNTHESIS OF ALDEHYDE ENAMINES IN HIGH YIELD AND HIGH PURITY
  202444. 1994X    1541
  202445. 1546Y
  202446. 14710
  202447. BATHINI, Y.
  202448. Syn. Commun.C
  202449. INVITRO AGENTS M
  202450. 15719N
  202451. 2/28/96
  202452. SYNTHETIC STUDIES TOWARDS TAXOL ANALOGS 
  202453.  CHEMOSELECTIVE CLEAVAGE OF C
  202454. 5 CINNAMOYL GROUP IN TAXANE GROUP OF DITERPENOIDS WITH HYDROXYLAMINE
  202455. 1994X    1513
  202456. 1517Y
  202457. 14711
  202458. KANG, K. T.
  202459. Syn. Commun.M
  202460. 15720N
  202461. 2/28/96
  202462. SYNTHESIS OF b
  202463. TRIMETHYLSILYL
  202464. UNSATURATED KETONES VIA LEWIS ACID PROMOTED REACTIONS OF 2,3
  202465. BIS(TRIMETHYLSILYL)PROPENE WITH ACID CHLORIDES
  202466. 1994X    1507
  202467. 1512Y
  202468. 14712
  202469. CHUANG, C. P.
  202470. Syn. Commun.C
  202471. ORGANIC SYNTHESIS CYCLIZATION M
  202472. 15721N
  202473. 2/28/96
  202474. AfMANGANESE(III) ACETATE INITIATED OXIDATIVE FREE RADICAL REACTION OF 3
  202475. HETEROARYL SUBSTITUTED MALONATES
  202476. 1994X    1493
  202477. 1505Y
  202478. 14713
  202479. BUTLER, A.
  202480. Chem. Rev.M
  202481. 15722N
  202482. 2/28/96V
  202483. VANADIUM PEROXIDE COMPLEXESW
  202484. 1994X
  202485. 14714
  202486. ARNOLD, D. P.
  202487. Aust. J. Chem.M
  202488. 15723N
  202489. 2/28/96
  202490. A7DERIVATIVES OF 4
  202491. (AMINOMETHYL)PYRROLE
  202492. CARBOXYLIC ACID
  202493. 1994X
  202494. 14715
  202495. ARNOLD, D. P.
  202496. Aust. J. Chem.CJ3,4
  202497. DISUBSTITUTED PYRROLES 
  202498. NITROALKENES 
  202499. DERIVATIVES 
  202500. CHEMISTRY 
  202501. ALKENES M
  202502. 15724N
  202503. 2/28/96
  202504. A=THE PREPARATION OF PYRROLE
  202505. CARBOXYLATES FROM VINYL SULFONES
  202506. 1994X
  202507. 14716
  202508. ANDERTON, N.
  202509. Aust. J. Chem.M
  202510. 15725N
  202511. 2/28/96
  202512. AOTHE INCLUSION OF PYRROLIZIDINE ALKALOIDS BY A
  202513. CYCLODEXTRINS AND b
  202514. CYCLODEXTRINS
  202515. 1994X
  202516. 14717
  202517. Pich, K. C.B
  202518. Aust. J. Chem.C
  202519. ANALOGS 
  202520. AGENTS M
  202521. 15726N
  202522. 2/28/96
  202523. AeRITTER REACTIONS .9. TRANSANNULAR ADDITION OF NITRILES TO THE 5H
  202524. DIBENZO[A,D]CYCLOHEPTENE RING SYSTEM
  202525. 1994X
  202526. 14718
  202527. A    WEISS, R.
  202528. Angew. Chem. Int. Ed. Engl. M
  202529. 15727N
  202530. 2/28/96
  202531. A]CONCERNING THE MECHANISM OF A
  202532. ELIMINATION: HYPERVALENT ION FAIRING IN AN IODOCARBENIUM IODIDE
  202533. 14719
  202534. Yoon, T.B
  202535. Angew. Chem. Int. Ed. Engl. M
  202536. 15728N
  202537. 2/28/96
  202538. AXA CONCISE TOTAL SYNTHESIS OF (+/
  202539. MAMANUTHAQUINONE BY USING AN EXO
  202540. DIELS
  202541. ALDER REACTION
  202542. 1994X
  202543. 14720
  202544. A    SMITH, K.
  202545. Angew. Chem. Int. Ed. Engl. M
  202546. 15729N
  202547. 2/28/96
  202548. AmSYNTHESIS AND PROPERTIES OF 2,4,6
  202549. TRIMETHYLPHENYLBORANE (MESITYLBORANE), A STABLE ALTERNATIVE TO THEXYLBORANE
  202550. 1994X
  202551. 14721
  202552. MARKO, I. E.
  202553. Tet. Lett.C
  202554. LANTHANIDE 
  202555. CYCLOADDITION REACTIONS BETWEEN 5
  202556. CMP 1 AND VARIOUS VINYL ETHERS AND VINYL SULPHIDES, CATALYSED BY THE YB(OTF)3
  202557. BINOL COMPLEX, AFFORD BICYCLIC LACTONES 3 IN MODERATE TO EXCELLENT ENANTIOMERIC EXCESSES
  202558. 15730N
  202559. 2/28/96
  202560. AuCATALYTIC, ENANTIOSELECTIVE, INVERSE ELECTRON
  202561. DEMAND DIELS
  202562. ALDER (IEDDA) REACTIONS OF 3
  202563. CARBOMETHOXY
  202564. PYRONE (3
  202565. 1994X    2771
  202566. 2774Y
  202567. 14722
  202568. BACIOCCHI, E.
  202569. Tet. Lett.
  202570. UAN EFFICIENT SYNTHESIS OF G
  202571. HALOESTERS HAS BEEN ACHIEVED, UNDER VERY MILD CONDITIONS, BY ADDITION OF ELECTROPHILIC CARBON RADICALS 
  202572. CH(R)CO2ET (R=H, ME, CO2ET) GENERATED BY XCH(R)CO2ET (X=BR, I) / BET3 / AIR IN DMSO TO ALKENES AND CYCLOALKENES. THE SYNTHESIS OF G
  202573. KETOESTERS IS ALSO POSSIBLE WHEN SILYL ENOL ETHERS ARE USED AS THE SUBSTRATES
  202574. 15731N
  202575. 2/28/96
  202576. SYNTHESIS OF g
  202577. HALOESTERS AND g
  202578. KETOESTERS BY HOMOLYTIC ADDITION OF CARBON RADICALS GENERATED BY A
  202579. HALOESTERS AND TRIETHYLBORANE TO ALKENES AND SILYL ENOL ETHERS
  202580. 1994X    2763
  202581. 2766Y
  202582. 14723
  202583. A    MEHTA, G.
  202584. Tet. Lett.
  202585. A]A SEQUENCE FOR GENERATING THE DOLABELLANE DITERPENE FRAMEWORK FROM (R)
  202586. LIMONENE IS DELINEATED
  202587. 15732N
  202588. 2/28/96
  202589. AwAN OXY
  202590. COPE REARRANGEMENT ROUTE FOR THE ENANTIOSELECTIVE CONSTRUCTION OF 5,11
  202591. FUSED FRAMEWORK OF DOLABELLANE DITERPENES
  202592. 1994X    2761
  202593. 2762Y
  202594. 14724
  202595. A    BROWN, A.
  202596. Tet. Lett.C
  202597. SYSTEMS 
  202598. RING 
  202599. 'CYCLISATION
  202600. CARBOMETHOXYLATION CAN SUCCESSFULLY COMPETE WITH 3
  202601. TRIG CYCLISATION OF ORGANOPALLAdium(II) SPECIES. CYCLISATION WITH ANION TRANSFER FROM BORON CAN BE ACHIEVED IN HIGH YIELD IN COMPETITION WITH A 3
  202602. TRIG CYCLISATION PROCESS THAT LACKS A SUBSEQUENT B
  202603. HYDRIDE ELIMINATION PATHWAY
  202604. 15733N
  202605. 2/28/96
  202606. AmPALLADIUM CATALYSED CYCLISATION
  202607. CYCLOPROPANATION AND CYCLIZATION 
  202608.  ANION CAPTURE PROCESSES OF VINYL TRIFLATES
  202609. 1994X    2753
  202610. 2756Y
  202611. 14725
  202612. HEANEY, H.
  202613. Tet. Lett.C
  202614. ETHERS 
  202615. REACTIONS OF PYROPHOSPHORYL CHLORIDE WITH AMIDES DERIVED FROM ARYLETHYLAMINES AND RELATED COMPOUNDS WITH 2
  202616. METHOXYCARBONYLBENZOYL CHLORIDE GIVE THE EXPECTED BISCHLER
  202617. NAPIERALSKI PRODUCTS IN GOOD YIELDS WHICH THEN ISOMERISE READILY TO AFFORD N
  202618. ACYLAMINOL ETHERS UNDER BASE CATALYSIS;  ACYLIMINIUM IONS ARE THEN GENERATED USING TRIMETHYLSILYL TRIFLATE AND CAPTURED, FOR EXAMPLE WITH ALLYLTRIMETHYLSILANE
  202619. 15734N
  202620. 2/28/96
  202621. A\ACYLIMINIUM IONS DERIVED FROM THE REARRANGEMENT OF BISCHLER
  202622. NAPIERALSKI CYCLISATION PRODUCTS
  202623. 1994X    2751
  202624. 2752Y
  202625. 14726
  202626. Reis, L. V.B
  202627. Tet. Lett.C*ACYLATION
  202628. REARRANGEMENT NITRONES 
  202629. KETONES 
  202630. ENEHYDROXYLAMINES REACT READILY, IN THE PRESENCE OF BASE, WITH ELECTROPHILES CONTAINING UNSATURATION TO AFFORD INTERMEDIATES THAT, EITHER SPONTANEOUSLY OR UPON HEATING, LEAD VIA A 3,3
  202631. SIGMATROPIC REARRANGEMENT TO A
  202632. SUBSTITUTED PRODUCTS
  202633. 15735N
  202634. 2/28/96
  202635. AJENEHYDROXYLAMINES AS VERSATILE COMPOUNDS IN 3,3
  202636. SIGMATROPIC REARRANGEMENTS
  202637. 1994X    2747
  202638. 2750Y
  202639. 14727
  202640. OSBORN, H. M. I.
  202641. Tet. Lett.
  202642. THE RING
  202643. OPENING REACTION OF N
  202644. DIPHENYLPHOSPHINOYLAZIRIDINES BY COPPER (i)
  202645. MODIFIED GRIGNARD REAGENTS PROCEEDS IN GOOD TO EXCELLENT YIELD AND WITH COMPLETE REGIOSPECIFICITY
  202646. 15736N
  202647. 2/28/96
  202648. A PRACTICAL ALTERNATIVE TO SULFONYL ACTIVATION OF AZIRIDINES 
  202649.  RING
  202650. OPENING OF N
  202651. DIPHENYLPHOSPHINOYL AZIRIDINES BY CARBON NUCLEOPHILES
  202652. 1994X    2739
  202653. 14728
  202654. PALOMO, C.
  202655. Tet. Lett.C
  202656. AMINOPEPTIDASE 
  202657. A NEW SYNTHESIS OF A,B
  202658. DIAMINO
  202659. HYDROXYACIDS THROUGH OPTICALLY PURE NON
  202660. NATURALLY AVAILABLE AMINO ACID
  202661. DERIVED N
  202662. CARBOXYANHYDRIDES (NCAS) IS DESCRIBED
  202663. 15737N
  202664. 2/28/96
  202665. AbFROM (S)
  202666. AMINO-b
  202667. HYDROXYACIDS TO (R)
  202668. DIAMINO
  202669. HYDROXYACID N
  202670. CARBOXYANHYDRIDES VIA b
  202671. LACTAMS
  202672. 1994X    2725
  202673. 2728Y
  202674. 14729
  202675. PALOMO, C.
  202676. Tet. Lett.C^AMINO
  202677. ACIDS STEREOSELECTIVE SYNTHESIS OZONIDE FRAGMENTATION ANHYDRIDES 
  202678. OZONOLYSIS 
  202679. ACETONIDE 
  202680. AkA NEW SYNTHESIS OF A
  202681. AMINO
  202682. HYDROXY ACID
  202683. CARBOXYANHYDRIDES FROM NON
  202684. AMINO ACID PRECURSORS IS DESCRIBED
  202685. 15738N
  202686. 2/28/96
  202687. SYNTHESIS OF B
  202688. ALKYLSERINE
  202689. CARBOXYANHYDRIDES THROUGH b
  202690. LACTAMS VIA CYCLOADDITION REACTION OF ALKOXYKETENES TO CHIRAL A
  202691. ALKOXYALDEHYDE
  202692. DERIVED IMINES
  202693. 1994X    2721
  202694. 2724Y
  202695. 14730
  202696. KITA, Y.
  202697. Tet. Lett.C
  202698. NUCLEOPHILIC 
  202699. VINYLIC SUBSTITUTIONS HYPERVALENT IODINE ORGANIC SYNTHESIS EFFICIENT CONVERSION 
  202700. KETO GROUPS CONFIGURATION 
  202701. OXIDATION 
  202702. HALIDES 
  202703. THE IN SITU REACTION OF A NOVEL HYPERVALENT IODINE REAGENT 2B HAVING AN ARYLTHIO LIGAND, PREPARED FROM PHENYLIODINE DIACETATE AND 2,3,5,6
  202704. TETRAFLUOROTHIOPHENOL 1B IN PYRIDINE, WITH 1
  202705. ALKYNES 3 GAVE 1,2
  202706. BIS(ARYLTHIO)ALKENES 4 IN GOOD YIELDS
  202707. 15739N
  202708. 2/28/96
  202709. AoPREPARATION OF bIS(ARYLTHIO)IODOBENZENE AND REACTION WITH 1
  202710. ALKYNES 
  202711.  A NOVEL ROUTE TO 1,2
  202712. bIS(ARYLTHIO)ALKENES
  202713. 1994X    2717
  202714. 2720Y
  202715. 14731
  202716. NAKATSUKA, S.
  202717. Tet. Lett.
  202718. ACYLINDOLES REACT REGIOSELECTIVELY WITH A
  202719. HALOGENOACYL CHLORIDE IN THE PRESENCE OF ALUMINUM CHLORIDE TO PRODUCE 1
  202720. HALOGENOACYLINDOLES IN EXCELLENT
  202721. 15740N
  202722. 2/28/96
  202723. A-FORMATION OF 6
  202724. ACYLINDOLES FROM 1
  202725. ACYLINDOLES
  202726. 1994 X    2699
  202727. 2700Y
  202728. 14732
  202729. GLASS, T. E.
  202730. Tet. Lett.C
  202731. CYCLOPENTADIENE THERMOLYSIS 
  202732. THE TItlE COMPOUND, WHEN SUBJECTED TO GAS
  202733. PHASE PYROLYSIS AT 275 
  202734.  C, UNDERGOES PREDOMINANTLY FRAGMENTATION TO CYCLOPENTADIENE AND ISOBUTYLENE
  202735. 15741N
  202736. 2/28/96
  202737. AATHE THERMAL REARRANGEMENT OF 7,7
  202738. DIMETHYLBICYCLO[3.2.0]HEPT
  202739. 1994X    2675
  202740. 2678Y
  202741. 14733
  202742. GRIECO, P. A.
  202743. Tet. Lett.C
  202744. LEWIS ACID 
  202745. THE ADDITION OF 1.0
  202746. 10 MOL% OF CAMPHORSULFONIC ACID TO 5.0 M LITHIUM PERCHLORATE IN DIETHYL ETHER DRAMATICALLY ACCELERATES INTRAMOLECULAR DIELS
  202747. ALDER REACTIONS AND ENHANCES THE ENDO
  202748. EXO SELECTIVITY
  202749. 15742N
  202750. 2/28/96
  202751. ACID CATALYZED INTRAMOLECULAR DIELS
  202752. ALDER REACTIONS IN LITHIUM PERCHLORATE
  202753. DIETHYL ETHER 
  202754.  ENHANCED REACTION RATES AND DIASTEREOSELECTIVITY
  202755. 1994X    2663
  202756. 2666Y
  202757. 14734
  202758. HUBER, R. S.
  202759. Tet. Lett.
  202760. [BIS (TRIMETHYLSILYL)] 
  202761. DIYNE HAS BEEN PREPARED IN HIGH YIELD AND IN ONE POT FROM TRIMETHYLSILYLPROPARGYL BROMIDE BY A REMARKABLY STEREOSELECTIVE TANDEM CARBENOID COUPLING
  202762. HX ELIMINATION SEQUENCE
  202763. 15743N
  202764. 2/28/96
  202765. A MILD AND EFFICIENT ROUTE TO THE PHARMACOPHORE OF THE ENEDIYNE ANTITUMOR AGENTS 
  202766. [BIS(TRIMETHYLSILYL)]
  202767. DIYNE VIA A NOVEL CARBENOID COUPLING REACTION
  202768. 1994X    2655
  202769. 2658Y
  202770. 14735
  202771. PETERSON, A. C.
  202772. Tet. Lett.C.BIOMIMETIC CONSTRUCTION SKELETON 
  202773. LIGAND 
  202774. THE OPTICALLY ACTIVE N
  202775. METHYL, N
  202776. BENZYLTETRACYCLIC KETONE 1 WAS CONVERTED INTO EITHER DIASTEREOMERIC SPIROCYCLIC OXINDOLE 2A (91:  9) OR 2B (97:  3) WITH HIGH DIASTEREOSELECTIVITY ON PRUDENT CHOICE OF OSMIUM REAGENTS. OXINDOLE 2A IS NOW AVAILABLE IN ENANTIOSPECIFIC FORM FOR THE SYNTHESIS OF ALSTONIA ALKALOIDS WHILE DIASTEREOMER 2B CAN BE EMPLOYED FOR THE PREPARATION OF GARDNERIA AND VOACANGA BASES
  202777. 15744N
  202778. 2/28/96
  202779. A>STUDIES ON THE ENANTIOSPECIFIC SYNTHESIS OF OXINDOLE ALKALOIDS
  202780. 1994X    2651
  202781. 2654Y
  202782. 14736
  202783. SLACK, W. E.
  202784. Tet. Lett.
  202785. THE PRODUCTS AND STEREOCHEMISTRIES OF CARBENIC DECOMPOSITIONS OF VARIED 2
  202786. DIAZOALKANES AND 1
  202787. DIAZO
  202788. HETARYL)PROPANES HAVE BEEN DETERMINED
  202789. 15745N
  202790. 2/28/96
  202791. A\THE STEREOCHEMISTRY OF REARRANGEMENTS OF ARYL AND HETARYL GROUPS TO PRIMARY CARBENIC CENTERS
  202792. 1994X    2647
  202793. 2650Y
  202794. 14737
  202795. PEARSON, W. H.
  202796. Tet. Lett.C
  202797. PROTONATED 
  202798. AZOMETHINE YLIDES NONSTABILIZED NITRILE YLIDES CYCLOADDITIONS DESILYLATION REACTION SILICON 
  202799. ROUTES 
  202800. IMMONIUM SALTS EQUIVALENTS
  202801.  METHYLIDES 
  202802. PYRROLIDINES 
  202803. RETRONECINE 
  202804. IMIDATES AND THIOIMIDATES 1 BEARING AN N
  202805. BUTYLSTANNYL)ALKYL GROUP (E.G., 7
  202806. 9) WERE TRANSMETALATED WITH N
  202807. BULI TO GENERATE HETEROATOM
  202808. SUBSTITUTED 2
  202809. AZAALLYL ANIONS 2. THESE ANIONS UNDERWENT [2 p S+4 p S] CYCLOADDITIONS WITH ALKENES TO PRODUCE 1
  202810. PYRROLINES 4 AFTER LOSS OF ALKOXIDE OR THIOLATE. THE PYRROLINES WERE FURTHER DEPROTONATED IN SITU WITH N
  202811. BULI TO GENERATE 1
  202812. METALLOENAMINES 5, WHICH COULD BE QUENCHED WITH WATER OR CH3I TO PRODUCE 1
  202813. PYRROLINES 4 OR 6. THE USE OF DIPHENYLACETB*YLENE IN THE CYCLOADDITION RESULTED IN THE
  202814. 15746N
  202815. 2/28/96
  202816. GENERATION AND CYCLOADDITION OF HETEROATOM
  202817. SUBSTITUTED 2
  202818. AZAALLYL ANIONS WITH ALKENES AND ALKYNES 
  202819.  SYNTHESIS OF 1
  202820. PYRROLINES AND PYRROLES
  202821. 1994X    2641
  202822. 2644Y
  202823. 14738
  202824. RASTELLI, A.
  202825. Tetrahedron
  202826. THE REACTION OF DIAZOMETHANE WITH ALLENE AT ROOM TEMPERATURE AFFORDED A MIXTURE OF 4
  202827. METHYLENE
  202828. PYRAZOLINE (1) AND 3
  202829. METHYLENE
  202830. PYRAZOLINE (2) IN A 93:  7 RATIO. THIS FINDING REVISES LITERATURE DATA WHICH DESCRIBE THIS REACTION AS REGIOSPECIFIC WITH EXCLUSIVE FORMATION OF 1. GOOD LEVEL AB
  202831. INITIO CALCULATIONS (E.G., HF/6
  202832. 31G*//HF/6
  202833. 31G*, MP4SDTQ/6
  202834. 31G*//HF/6
  202835. 31G* AND MP4SDTQ/6
  202836. 31G*//MCSCF/3
  202837. 21G) QUALITATIVELY REPRODUCE THE EXPERIMENTAL REGIOCHEMICAL RATIO
  202838. 15747N
  202839. 2/28/96
  202840. AfTHEORETICAL AND EXPERIMENTAL STUDY OF THE REGIOSELECTIVITY OF THE REACTION OF DIAZOMETHANE WITH ALLENE
  202841. 1994X    5561
  202842. 14739
  202843. ALCAIDE, B.
  202844. TetrahedronC}REGIOCHEMICAL CONTROL CHELATING PROCESSES CIS
  202845. OXIDES 
  202846. EPOXIDES 
  202847. ACID 
  202848. EPOXIDES METHANOLYSIS 
  202849. EFFICIENT CATALYST 
  202850. SOLVENT 
  202851. 7A KINETIC STUDY OF THE UNCATALYZED METHANOLYSIS OF FURYL
  202852. OXIRANE HAS BEEN ACHIEVED, GIVING INFORMATION ABOUT THE MECHANISM OF A ''PURE'' (UNCATALYZED) RING OPENING OF A HETEROAROMATIC OXIDE. SOLVENT AND SALT EFFECT ARE COMPATIBLE WITH A SOLVENT ASSISTED PROCESS WITH A SOLVENT
  202853. SEPARATED ION
  202854. PAIR INTERMEDIATE.
  202855. 15748N
  202856. 2/28/96
  202857. AZTHE UNCATALYZED ALCOHOLYSIS OF FURYL
  202858. OXIRANE 
  202859.  A MECHANISTIC STUDY BASED ON KINETIC DATA
  202860. 1994X    5555
  202861. 5560Y
  202862. 14740
  202863. HAQUE, M. R.
  202864. Tetrahedron
  202865. TRANSITION STATE STRUCTURES 
  202866. SELECTIVITY PRINCIPLE NUCLEOPHILIC SUBSTITUTION METHYL TRANSFER N
  202867. METHYLATION 
  202868. SN2 REACTIONS 
  202869. PYRIDINES 
  202870. MECHANISM 
  202871. MODEL 
  202872. THE REGIOSELECTIVITIES WERE DETERMINED FOR ALKYLATIONS OF 4
  202873. METHYL
  202874. , 2,4
  202875. DIMETHYL
  202876. AMINO
  202877. METHL
  202878. CHLORO
  202879. METHYL
  202880. ETHOXY
  202881. METHYL
  202882. BENZIMIDAZOLE, AND 4
  202883. METHYLBENZIMIDAZOLONE (AS ANIONS IN DIMETHYLFORMAMIDE) WITH A VARIETY OF PRIMARY ALKYLATING AGENTS. THESE N1/N3 REGIOSELECTIVITIES ARE CORRELATED WITH THE SECOND ORDER RATE CONSTANTS FOR BENZYLATION (BENZYL CHLORIDE / DIMETHYLFORMAMIDE / 30 
  202884. C) OF THESE HETEROCYCLIC ANIONS UNDER COMPARABLE CONDITIONS. ALTERING THE ALKYLATING AGENT,B* R'CH2CL, CAUSES MOVEMENT ALONG THE LOOSE
  202885. 15749N
  202886. 2/28/96
  202887. AUAMBIDENT HETEROCYCLIC REACTIVITY 
  202888.  ALKYLATION OF 2
  202889. SUBSTITUTED
  202890. METHYLBENZIMIDAZOLES
  202891. 1994X    5535
  202892. 5554Y
  202893. 14741
  202894. LAMARA, K.
  202895. TetrahedronC1LOW
  202896. TEMPERATURE MATRICES 
  202897. ARYL 
  202898. AZIDES 
  202899. AZEPINES 
  202900. UNLIKE OTHER ARYL AZIDES BEARING ELECTRON
  202901. WITHDRAWING ORTHO
  202902. SUBSTITUENTS, O
  202903. AZIDOBENZONITRILES ON PHOTOLYSIS IN AQUEOUS
  202904. TETRAHYDROFURAN YIELD MIXTURES OF THE EXPECTED 3
  202905. CYANO
  202906.  AND THE UNEXPECTED 7
  202907. CYANO
  202908. AZEPIN
  202909. 2(1H)
  202910. ONES. IN ONE INSTANCE RING
  202911. CONTRACTION TO A 2
  202912. AZABICYCLO[3.2.0]HEPT
  202913. ONE IS NOTED. X
  202914. RAY CRYSTALLOGRAPHIC DATA FOR 7
  202915. CYANO
  202916.  AND 4
  202917. CHLORO
  202918. CYANO
  202919. AZEPIN
  202920. ONE, AND FOR THE AZABICYCLOHEPTENONE, ARE PRESENTED
  202921. 15750N
  202922. 2/28/96
  202923. AZEPINES AND RELATED SYSTEMS .5. PHOTOiNDUCED RING EXPANSIONS OF O
  202924. AZIDOBENZONITRILES TO 3
  202925. CYANO
  202926.  AND 7
  202927. CYANO
  202928. AZEPIN
  202929. 2(1H)
  202930. 1994X    5515
  202931. 5526Y
  202932. 14742
  202933. CHIACCHIO, U.
  202934. TetrahedronC9CYCLOADDITION 
  202935. DIPOLAR CYCLOADDITION ALCOHOLS 
  202936. ROUTE 
  202937. A SERIES OF NITRONES 5 JOINED BY AMIDES TO OLEFINS WERE PREPARED IN SITU FROM THE RELATED ALDEHYDES WITH N
  202938. METHYLHYDROXYLAMINE. THE NITRONES ADDED INTRAMOLECULARLY TO THE OLEFIN, AND THE CYCLOADDITIONS GAVE FUSED G
  202939. LACTAMS 6 STEREOSELECTIVELY. A STEREOCENTer LOCATED IN POSITION A TO THE NITRONIC FUNCTIONALITY 13 COMPLETELY CONTROLS THE STEREOCHEMICAL COURSE OF THE INTRAMOLECULAR CYCLOADDITION, WHICH EXCLUSIVELY AFFORDS COMPOUND 14 WITH SIMULTANEOUS INTRODUCTION OF FOUR STEREOCENTerS. THE FB6ORMATION OF THIS LATTER COMPOUND WAS ALSO SUPPORTED BY
  202940. 15751N
  202941. 2/28/96
  202942. ATSTEREOSELECTIVE SYNTHESIS OF FUSED g
  202943. LACTAMS BY INTRAMOLECULAR NITRONE CYCLOADDITION
  202944. 1994X    5503
  202945. 5514Y
  202946. 14743
  202947. FREDERICKSON, M.
  202948. TetrahedronC
  202949. OXIMES 
  202950. TANDEM NITRONE GENERATION/CYCLOADDITION REACTIONS BETWEEN SIMPLE SUGAR ALDOXIMES AND DIVINYL SULPHONE IN REFLUXING TOLUENE HAVE BEEN SHOWN TO OCCUR REGIOSPECIFICALLY AND WITH HIGH DIASTEREOSELECTIVITY IN THE CYCLOADDITION STEP TO AFFORD HOMOCHIRAL CYCLOADDUCTS IN GOOD YIELD. THE PROCESS IS APPLICABLE TO BOTH FURANOSE AND PYRANOSE ALDOXIMES. ABSOLUTE STEREOCHEMISTRIES OF THE PRODUCTS HAVE BEEN DETERMINED BY NOE SPECTROSCOPY AND X
  202951. RAY CRYSTALLOGRAPHY
  202952. 15752N
  202953. 2/28/96
  202954. ANHOMOCHIRAL CYCLOADDUCTS DERIVED FROM SUGAR ALDOXIMES VIA NITRONE INTERMEDIATES
  202955. 1994X    5495
  202956. 5502Y
  202957. 14744
  202958. A    GRIGG, R.
  202959. TetrahedronCgENANTIOSELECTIVE ADDITION PHYTOTOXIC 
  202960. BUTENOLIDES SEIRIDIUM
  202961. CARDINALE REAGENTS 
  202962. ALDEHYDES 
  202963. ROUTE 
  202964. ARYL 
  202965. ~PD(O) CATALYSED CROSS
  202966. COUPLING OF BUTENOLIDE
  202967. TRIFLATES TO 9
  202968. ALKYL
  202969. BOROBICYCLO[3.3.1] NONANES OCCURS IN MODERATE TO GOOD YIELD AND TOLERATES A RANGE OF FUNCTIONALITY. APPLICATION OF THIS METHODOLOGY COMBINED WITH ADDITION OF DIETHYLZINC TO A BUTENOLIDE ALDEHYDE IN THE PRESENCE OF ON EPHEDRINE DERIVATIVE LEADS TO A 3
  202970. STEP SYNTHESIS OF (
  202971. ISOSEIRIDINE WITH 88%E.E. IN GOOD YIELD
  202972. 15753N
  202973. 2/28/96
  202974. PALLADIUM CATALYSED CROSS
  202975. COUPLING OF VINYL TRIFLATES WITH 9
  202976. ALKYL
  202977. BOROBICYCLO[3,3,1]NONANES 
  202978.  TOTAL SYNTHESIS OF (
  202979. ISOSEIRIDINE
  202980. 1994X    5489
  202981. 5494Y
  202982. 14745
  202983. BARILLIER, D.
  202984. Tetrahedron
  202985. EPOXYSULFOXIDE b
  202986. KETO SULFIDE 
  202987. KETO VINYLTHIOETHER HALIDE
  202988. BASED ELECTROPHILE DEOXYGENATION DEHYDRATION 
  202989. THIONIUM IONS 
  202990. KETO TRANSPOSITION ORGANIC SYNTHESIS SODIUM IODIDE 
  202991. NEW SYNTHESES OF A
  202992. THIOSUBSTITUTED CARBONYL COMPOUNDS WITH THE CARBONYL CARBON BEING THE ONE THAT ORIGINALLY DOES NOT CARRY THE SULFOXIDE GROUP FROM SIX
  202993. MEMBERED RING A,b
  202994. EPOXYSULFOXIDES AND SEVERAL HALIDES
  202995. BASED ELECTROPHILES ARE DESCRIBED. MECHANISTIC CONSIDERATIONS FOR DEOXYGENATION AS WELL AS DEHYDRATION REACTIONS ARE ALSO DISCUSSED. IN ADDITION, METHODOLOGY FOR ACHIEVING 1,2
  202996. CARBONYL TRANSPOSITION STARTING WITH ISOMERICALLY PURE CYCLOHEXENYL SULFIDES DERIVED FROM ISOPHORONE AND CHOLESB
  202997. ONE IS BRIEFLY REPORTED
  202998. 15754N
  202999. 2/28/96
  203000. HALIDE
  203001. BASED ELECTROPHILES MEDIATED EPOXIDE RING
  203002. OPENING REACTIONS OF A,b
  203003. EPOXYSULFOXIDES IN C
  203004. SERIES 
  203005.  DEOXYGENATION VERSUS DEHYDRATION AND AN OVERALL 1,2
  203006. KETO TRANSPOSITION
  203007. 1994X    5413
  203008. 5424Y
  203009. 14746
  203010. A    SEVIN, A.
  203011. TetrahedronC
  203012. CARBONYL
  203013. COMPOUNDS TRANSITION
  203014. STATE SECONDARY ENAMINES PROTON AFFINITY 
  203015. REACTION PATHS 
  203016. INITIO 
  203017. ADDITIONS 
  203018. ORIGIN 
  203019. STEREOSELECTIVITY STEREOCHEMISTRY 
  203020. MOROKUMA'S ENERGY PARTITION SCHEME HAS BEEN USED TO CALCULATE THE ELECTROSTATIC (ES), POLARIZATION (PL), EXCHANGE (EX), AND CHARGE TRANSFER (CT) COMPONENTS OF THE TOTAL ENERGY OF INTERACTION FOR VARIOUS COMPLEXES BETWEEN NUCLEOPHILES (VINYLAMINES, VINYLOL) AND ELECTROPHILES (BH3, FORMALDEHYDE, CL2, METHYLCHLORIDE, CH3+ AND NH4+). SIMPLE GEOMETRY VARIATIONS HAVE BEEN MADE IN ORDER TO DETERMINE THEIR INFLUENCE ON THE STUDIED COMPLEXES. WHEN DEALING WITH VINYLAMINE, THE ROLE OF NITROGEN PYRAMB4IDALIZATION COMPLEXES HAS BEEN STUDIED. A PARTICULAR
  203021. 15755N
  203022. 2/28/96
  203023. A]ON THE NATURE OF THE ELECTRONIC INTERACTION BETWEEN CONJUGATED NUCLEOPHILES AND ELECTROPHILES
  203024. 1994X    5387
  203025. 5400Y
  203026. 14747
  203027. LESUEUR, C.
  203028. TetrahedronC
  203029. C BOND FORMATION ADDITION
  203030. ELIMINATION SEQUENCE 
  203031. ALLYLIC SULFONES 
  203032. ARRHENIUS PARAMETERS STEREO
  203033. SELECTIVITY ANOMERIC RADICALS REGIO
  203034. SELECTIVITY SULFUR
  203035. COMPOUNDS 
  203036. RATE CONSTANTS RING
  203037. CLOSURE 
  203038. THE RADICAL CYCLIZATION OF ALKYL HEX
  203039. ENOPYRANOSIDES PROVIDES A STEREOCONTROLLED ROUTE TO FUSED FURANOPYRANES. THE INTERMEDIATE RADICAL IS GENERATED EITHER VIA THE REDUCTION OF THE APPROPRIATE HALIDE BY TIN HYDRIDE OR VIA SULFONYL RADICAL ADDITION TO ALLYL HEX
  203040. ENOPYRANOSIDES. THE TWO METHODOLOGIES ARE COMPARED WITH RESPECT TO DIASTEREOSELECTIVITY. STEREOCONTROL IS DISCUSSED ON THE BASIS OF CONFORMATIONAL PREFERENCE IN THE TRANSITION STATE
  203041. 15756N
  203042. 2/28/96
  203043. A8STEREOCONTROL IN RADICAL CYCLIZATIONS ON SUGAR TEMPLATES
  203044. 1994X    5369
  203045. 5380Y
  203046. 14748
  203047. CHEMIN, D.
  203048. Tetrahedron
  203049. POTENT ANTITUMOR ANTIBIOTICS NEOCARZINOSTATIN CHROMOPHORE SEX
  203050. PHEROMONE CALICHEMICIN
  203051. G1 ESPERAMICINS 
  203052. CHEMISTRY 
  203053. DYNEMICIN FAMILY
  203054. THE STEREOSPECIFIC SEQUENTIAL SUBSTITUTION OF (E) AND (Z)
  203055. DICHLOROETHENES WITH 1
  203056. ALKYNES LEADS TO (E) AND (Z)
  203057. ENEDIYNES IN HIGH YIELD
  203058. 15757N
  203059. 2/28/96
  203060. PALLADIUM
  203061. CATALYZED REACTION OF (E) AND (Z)
  203062. DICHLOROETHENES WITH 1
  203063. ALKYNES 
  203064.  AN EFFICIENT STEREOSPECIFIC SYNTHESIS OF (E) AND (Z)
  203065. ENEDIYNES
  203066. 1994X    5335
  203067. 5344Y
  203068. 14749
  203069. KASHIMA, C.
  203070. B    Synthesis
  203071. (JANUARY, PG 61, 1994)
  203072. 15758N
  203073. 2/28/96
  203074. AFTHE PREPARATION OF N
  203075. ACYLPYRAZOLES AND THEIR BEHAVIOR TOWARD ALCOHOLS 
  203076. 1994X
  203077. 14750
  203078. CABEZAS, J. A.
  203079. B    SynthesisC
  203080. ACETYLENIC ETHERS STANNYLCUPRATION 
  203081. VINYL CUPRATES  
  203082. VINYL ETHERS 
  203083. SYNTHETIC APPLICATIONS STANNYL
  203084. CUPRATION 
  203085. ENOL ETHERS VINYLSTANNANES 
  203086. ALLENESM
  203087. 15759N
  203088. 2/28/96
  203089. AiREGIOSELECTIVE ADDITION OF STANNYLCYANOCUPRATES TO ACETYLENIC ETHERS 
  203090.  A CHEMICAL AND SPECTROSCOPIC STUDY
  203091. 1994X
  203092. 14751
  203093. DEKIMPE, N.
  203094. B    Synthesis
  203095. KETO ACETALS a,a
  203096. DIALKOXY IMINES PROTECTED a
  203097. DIONES a
  203098. BROMO
  203099. CHLORO KETONES a
  203100. BROMO
  203101. CHLORO IMINES 
  203102. ARYNIC CONDENSATION ARGINYL RESIDUES REARRANGEMENT DERIVATIVES 
  203103. KETOACETALS 
  203104. 15760N
  203105. 2/28/96
  203106. A3SYNTHESIS OF A,A
  203107. DIALKOXY IMINES AND A
  203108. KETO ACETALS
  203109. 1994X
  203110. 14752
  203111. LOFFLER, A.
  203112. B    Synthesis
  203113. PERCHLOROBUTENYNE N,N',N'
  203114. TRIMETHYL
  203115. (TRICHLORO
  203116. BUTEN
  203117. YNYL)HYDRAZINE N
  203118. (BUTADIYNYL)HYDRAZINE DERIVATIVES 1,1
  203119. DICHLORO
  203120. ALKEN
  203121. YNES 
  203122. CYCLOADDITIONS PERCHLOROBUTENYNE YNAMINES 
  203123. 15761N
  203124. 2/28/96
  203125. AD(1,3
  203126. BUTADIYNYL)HYDRAZINES 
  203127.  A NEW CLASS OF ELECTRON
  203128. RICH ALKADIYNES
  203129. 1994X
  203130. 14753
  203131. MATARE, G. J.
  203132. B    Synthesis
  203133. AxACYLATION 
  203134. ACYCLIC b
  203135. DIKETONES COPPER(II) CHELATE GEMINAL TRIKETONE C
  203136. REGIOSELECTIVITY TRIETHYLAMINE 
  203137. MALONATE 
  203138. LITHIUM 
  203139. 15762N
  203140. 2/28/96
  203141. AFACETYLATION OF b
  203142. DIKETONE COPPER(II) CHELATES BY TREATMENT WITH KETENE
  203143. 1994X
  203144. 14754
  203145. ATTANASI, O. A.
  203146. B    Synthesis
  203147. ALKOXYCARBONYLAZOALKENES AMINOCARBONYLAZOALKENES TOSYLHYDRAZONES BISHYDRAZONES a
  203148. AZINOHYDRAZONES ORGANIC SYNTHESIS METAL
  203149. IONS 3
  203150. OXOALKANAMIDES 
  203151. 15763N
  203152. 2/28/96
  203153. SIMPLE, HIGH
  203154. YIELD SYNTHESIS OF UNSYMMETRICALLY FUNCTIONALIZED BISHYDRAZONE AND A
  203155. AZINOHYDRAZONE DERIVATIVES BY REACTION OF ALKOXY
  203156.  AND AMINOCARBONYLAZOALKENES WITH TOSYLHYDRAZONES
  203157. 1994X
  203158. 14755
  203159. A    Xu, Y. C.B    Synthesis
  203160. AZISOTHIOCHROMAN 1
  203161. ANTHRACENO[2,3
  203162. C]THIOPYRAN 
  203163. POT SYNTHESIS DIBROMIDE 
  203164. THIOGLYCOLATE 
  203165. 15764N
  203166. 2/28/96
  203167. A2A FACILE SYNTHESIS OF 3
  203168. SUBSTITUTED ISOTHIOCHROMAN
  203169. 1994X
  203170. 14756
  203171. KULINKOVICH, O. G.
  203172. B    SynthesisCZ4
  203173. OXOALKANOATES CHLOROPROPENYL KETONES ACTIVATED CYCLOPROPANES ACIDS 
  203174. DERIVATIVES 
  203175. ESTERS M
  203176. 15765N
  203177. 2/28/96
  203178. A4A NEW CONVENIENT SYNTHESIS OF METHYL 4
  203179. OXOALKANOATES
  203180. 1994X
  203181. 14757
  203182. PRAJAPATI, D.
  203183. Indian J. Chem. Sect. BC
  203184. AZADIENES 
  203185. IMINES M
  203186. 15766N
  203187. 2/28/96
  203188. AoINVERSE ELECTRON DEMAND HETERO
  203189. DIELS
  203190. ALDER REACTION OF N
  203191. SULPHINYLANILINE WITH N
  203192. EPOXYISOINDOLINES
  203193. 1994X
  203194. 14758
  203195. JOSHI, K. C.
  203196. Indian J. Chem. Sect. BC0FLUORINE SPIROHETEROCYCLES DERIVATIVES 
  203197. INDOLES M
  203198. 15767N
  203199. 2/28/96
  203200. ANTHERMAL AND PHOTOCHEMICAL REACTION OF 1
  203201. ACETYLINDOLE
  203202. DIONE WITH PYRAZOLONE
  203203. 1994X
  203204. 14759
  203205. Rao, V. R.B
  203206. Indian J. Chem. Sect. BC
  203207. COUMARIN DERIVATIVES THIAZOLYL M
  203208. 15768N
  203209. 2/28/96
  203210. A/A FACILE ONE
  203211. POT SYNTHESIS OF PYRAZOLOTHIAZOLES
  203212. 1994X
  203213. 14760
  203214. A    SINGH, S.
  203215. Indian J. Chem. Sect. BM
  203216. 15769N
  203217. 2/28/96
  203218. A@SYNTHESIS OF NOVEL 3,6
  203219. DIARYLTETRAHYDRO
  203220. OXAZINE
  203221. THIONES
  203222. 1994X
  203223. 14761
  203224. PATON, R. M.
  203225. J.C.S. Chem. Commun.C,SUGARS 
  203226. CYCLOADDITION 
  203227. OSMYLATION 
  203228. ALCOHOLS M
  203229. 15770N
  203230. 2/28/96
  203231. A>THE NITRILE OXIDE ISOXAZOLINE ROUTE TO HIGHER
  203232. CARBON DIALDOSES
  203233. 1994X
  203234. 14762
  203235. ALCALDE, E.
  203236. J.C.S. Chem. Commun.M
  203237. 15771N
  203238. 2/28/96
  203239. AlNOVEL CAPTODATIVE METHYLENE COMPOUNDS 
  203240.  SPONTANEOUS OXIDATION OF 1
  203241. ALKYL
  203242. (AZOLYLMETHYL)PYRIDINIUM SALTS
  203243. 1994X
  203244. 14763
  203245. BENNETT, P.
  203246. J.C.S. Chem. Commun.M
  203247. 15772N
  203248. 2/28/96
  203249. AVMEDIUM
  203250. DEPENDENT TRAPPING OF DIAZOALKANE INTERMEDIATES DURING PHOTOLYSIS OF DIAZIRINES
  203251. 1994X
  203252. 14764
  203253. THOMPSON, S. H. J.
  203254. GALLAGHER
  203255. J.C.S. Chem. Commun.C]N
  203256. SUBSTITUTED PYRROLIDIN
  203257. ONES CASTANOSPERMINE TRIACETOXYBOROHYDRIDE STEREOISOMERS 
  203258. ANALOGS M
  203259. 15773N
  203260. 2/28/96
  203261. AaHYDROXY
  203262. DIRECTED KETONE REDUCTION 
  203263.  APPLICATION TO THE SYNTHESIS OF (+)
  203264. DIEPICASTANOSPERMINE
  203265. 1994X
  203266. 14765
  203267. "A    Wu, S. P.B
  203268. J.C.S. Chem. Commun.M
  203269. 15774N
  203270. 2/28/96
  203271. FORMATIONS OF AN [8p +4p ] CYCLOADDUCT VIA AN ELECTRON
  203272. TRANSFER MECHANISM AND A META
  203273. CYCLOADDUCT BY IRRADIATIONS OF TROPONE AND 9,10
  203274. DICYANOANTHRACENE
  203275. 1994X
  203276. 14766
  203277. AVERDUNG, J.
  203278. Chem. Ber.
  203279. FULLERENES 
  203280. AZIRINES 
  203281. PHOTOCHEMISTRY 
  203282. [3 + 2] CYCLOADDITIONS ELECTRON TRANSFER REACTIONS 
  203283. 60 BUCKMINSTERFULLERENE CARBON C60 M
  203284. 15775N
  203285. 2/28/96
  203286. AWPHOTOREACTIONS WITH C60
  203287. FULLERENE 
  203288.  [3+2] PHOTOCYCLOADDITION OF 2,3
  203289. DIPHENYL
  203290. AZIRINE
  203291. 1994X
  203292. 14767
  203293. A    DYKER, G.
  203294. Chem. Ber.
  203295. H ACTIVATION 
  203296. PALLADIUM CATALYSIS DOMINO COUPLING PROCESSES 
  203297. PALLADIUM(IV) INTERMEDIATES 
  203298. MECHANISM 
  203299. COMPLEXES 
  203300. HALIDES 
  203301. 15776N
  203302. 2/28/96
  203303. TRANSITION METAL
  203304. CATALYZED ANNULATION REACTIONS .7. PALLADIUM
  203305. CATALYZED C
  203306. H ACTIVATION AT METHOXY GROUPS 
  203307.  REGIOCHEMISTRY OF THE DOMINO COUPLING PROCESSES
  203308. 1994X
  203309. 14768
  203310. AUMANN, R.
  203311. Chem. Ber.M
  203312. 15777N
  203313. 2/28/96
  203314. ORGANIC SYNTHESES VIA TRANSITION METAL COMPLEXES .69. 2
  203315. (ACYLAMINO)ETHENYL KETENE IMINES FROM [2
  203316. (ACYLAMINO)ETHENYL]CARBENE COMPLEXES AND THEIR RING
  203317. CLOSING METATHESIS TO PYRROLES OR ELECTROCYCLIZATION TO 1,4
  203318. DIAMINONAPHTHALENES
  203319. 1994X
  203320. 14769
  203321. A    WELLE, F.
  203322. Chem. Ber.
  203323. C BOND CLEAVAGE
  203324. KINETICS OF HEATS OF FORMATION 
  203325. RADICALS
  203326. STABILITY OF CAPTODATIVE EFFECT 
  203327. GEMINAL SUBSTITUENTS
  203328. ENERGETIC INTERACTION OF FORCE
  203329. FIELD CALCULATIONS THERMOLABILE HYDROCARBONS THERMAL
  203330. STABILITY 
  203331. ALKYL RADICALS 
  203332. HEATS 
  203333. 15778N
  203334. 2/28/96
  203335. SUBSTITUENT EFFECTS ON THE STRENGTH OF C
  203336. C BONDS .14. KINETIC AND THERMODYNAMIC STABILITY OF 2,3
  203337. BIS(DIALKYLAMINO)
  203338. DIKETONES 
  203339.  ENERGY OF STABILIZATION OF A
  203340. DIALKYLAMINO-A
  203341. CARBONYLALKYL RADICALS WITH CAPTODATIVE SUBSTITUENTS
  203342. 1994X
  203343. 14770
  203344. A    GERST, M.
  203345. Chem. Ber.
  203346. AxMOLECULE
  203347. INDUCED RADICAL FORMATION
  203348. KINETICS OF CATALYSIS 
  203349. ESR SPECTROSCOPY RADICAL CLOCK 
  203350. ISOKINETIC RELATIONSHIP RATES 
  203351. 15779N
  203352. 2/28/96
  203353. BIMOLECULAR FORMATION OF RADICALS BY H
  203354. TRANSFER .7. BIMOLECULAR FORMATION OF RADICALS VIA H
  203355. TRANSFER WITH CATALYSIS BY 7H
  203356. BENZ[DE]ANTHRACENE
  203357. 1994X
  203358. 14771
  203359. PAULINI, K.
  203360. Chem. Ber.
  203361. OXAZINES 
  203362. BROMINATION
  203363. RADICAL 
  203364. SN2 REACTION DIASTEREOSELECTIVITY DIELS
  203365. ALDER REACTIONS EFFICIENT SYNTHESIS AMINO
  203366. ACIDS 
  203367. ALKENES 
  203368. STEREOSELECTIVITY 6H
  203369. OXAZINES 
  203370. 15780N
  203371. 2/28/96
  203372. DIASTEREOSELECTIVE RADICAL BROMINATION OF 5,6
  203373. DIHYDRO
  203374. OXAZINES AND SUBSEQUENT SUBSTITUTION REACTIONS WITH NITROGEN NUCLEOPHILES
  203375. 1994X
  203376. 14772
  203377. MASNYK, M.
  203378. Chem. Ber.
  203379. EPOXYALKYL)TRIMETHYLSILANE REACTIONS 
  203380. SULFONYL ANIONS 
  203381. ALLYLIC ALCOHOLS b,G
  203382. UNSATURATED 
  203383. ALKYL PHENYL SULFONES ALLYLIC SULFONES ALDEHYDES 
  203384. 15781N
  203385. 2/28/96
  203386. REACTION OF (A,b
  203387. EPOXYALKYL)SILANES WITH A
  203388. SULFONYL ANIONS IN THE PRESENCE OF A LEWIS ACID 
  203389.  A METHOD FOR THE SYNTHESIS OF (Z)
  203390. ALLYLIC ALCOHOLS AND b,g
  203391. UNSATURATED ALKYL PHENYL SULFONES
  203392. 1994X
  203393. 14773
  203394. ADAM, W.
  203395. Chem. Ber.
  203396. DIMETHYLDIOXIRANE 3
  203397. PHENYL
  203398. PHENYLSULFONYLOXAZIRIDINE 
  203399. TITANIUM ENOLATES ENANTIOSELECTIVE HYDROXYLATION 
  203400. HYDROXY CARBONYL COMPOUNDS 
  203401. HYDROXY CARBONYL COMPOUNDS 
  203402. ASYMMETRIC OXIDATION CARBOHYDRATE COMPLEXES a-ESTER 
  203403. 15782N
  203404. 2/28/96
  203405. ENANTIOSELECTIVE OXIDATION OF CHIRAL TITANIUM ENOLATES DERIVED FROM PROPIOPHENONE BY DIMETHYLDIOXIRANE OR 3
  203406. PHENYL
  203407. PHENYLSULFONYLOXAZIRDINE
  203408. 1994X
  203409. 14774
  203410. A    BOESE, R.
  203411. Chem. Ber.C
  203412. (TRIFLUOROMETHYLTHIO)CARBON CARBENIUM IONS ONE
  203413. ELECTRON OXIDATION SUPERACIDIC SYSTEMS 2,4,4
  203414. TRIFLUORO
  203415. DITHIETAN
  203416. YLIUM HEXAFLUOROARSENATE SYSTEM M
  203417. 15783N
  203418. 2/28/96
  203419. ACSYNTHESES AND REACTIONS OF FLUOROORGANIC ACYCLIC THIOCARBENIUM IONS
  203420. 1994X
  203421. 14775
  203422. GABBUTT, C. D.
  203423. TetrahedronC
  203424. THIONYL CHLORIDE 
  203425. CHLORO
  203426. CHLOROSULFENYLCHROMAN
  203427. ONES ARE EFFICIENTLY OBTAINED FROM CHROMAN
  203428. ONES BY TREATMENT WITH THIONYL CHLORIDE. DIRECT OXIDATION AFFORDS 3,3
  203429. DICHLOROCHROMAN-4
  203430. ONES, WHILST CONVERSION TO THE SULFENAMIDES PRIOR TO OXIDATION PROVIDES A FACILE ROUTE TO 3
  203431. CHLOROCHROMAN
  203432. 15784N
  203433. 2/28/96
  203434. A NEW REACTION OF A
  203435. CHLORO
  203436. CHLOROSULFENYL KETONES 
  203437.  FACILE SYNTHESES OF 3,3
  203438. DICHLORO
  203439.  AND 3
  203440. CHLORO
  203441. CHROMAN
  203442. ONES AND THIOCHROMAN
  203443. 1994X    5245
  203444. 5254Y
  203445. 14776
  203446. LAVILLA, R.
  203447. TetrahedronCDN
  203448. ALKYLPYRIDINIUM SALTS ALKALOID SYNTHESIS DERIVATIVES 
  203449. ELLIPTICINE 
  203450. YREDUCTION OF INDOLYLDIHYDRODYRIDINES 4 AND 5 SATISFACTORILY SAVE THE CORRESPONDING TETRAHYDROPYRIDINES 6 AND 7. A SIMILAR REDUCTION OF 4
  203451. INDOLYLMETHYL)
  203452.  DIHYDROPYRIDINES 3 WAS INEFFICIENT. IN CONTRAST, DIHYDROPYRIDINE 19 WAS REDUCED TO 23 AND THEN CYCLIZED TO PENTACYCLE 24. DIRECT CYCLIZATION OF 19 RESULTED IN TILE FORMATION OF IMIDE 21
  203453. 15785N
  203454. 2/28/96
  203455. A[NUCLEOPHILIC ADDITIONS TO PYRIDINIUM SALTS 
  203456.  REDUCTION OF THE INTERMEDIATE DIHYDROPYRIDINES
  203457. 1994X    5233
  203458. 5244Y
  203459. 14777
  203460. HEDENSTROM, E.
  203461. TetrahedronM
  203462. 15786N
  203463. 2/28/96
  203464. EFFICIENT OPENING OF TRANS
  203465. EPOXYBUTANE BY A HIGHER ORDER CUPRATE 
  203466.  SYNTHESIS OF ERYTHRO
  203467. DIMETHYLPENTADECAN
  203468. YL ACETATE, PHEROMONE OF PINE SAWFLIES
  203469. 1994X    5225
  203470. 5232Y
  203471. 14778
  203472. VANAKEN, K. J.
  203473. Tetrahedron
  203474. AJCATALYZED REACTIONS ORGANOTIN COMPOUNDS 2H
  203475. OXAZIN
  203476. ONES CYANOHYDRINS 
  203477. SELECTIVE FUNCTIONALISATION OF THE CHLORIMINE GROUP IN 2,5
  203478. DICHLORO
  203479. METHYL
  203480. OXAZIN
  203481. ONE IS USUALLY REALISED IN APPROPRIATE CONDITIONS, BY ELECTROPHILIC CATALYSIS AVOIDING REACTION OF THE LACTONE FUNCTION. THE AZADIENE SYSTEM IN THE 3
  203482. SUBSTITUTED 5
  203483. CHLORO
  203484. METHYL
  203485. OXAZIN
  203486. ONES IS SHOWN TO REACT EASILY WITH MONOSUBSTITUTED ACETYLENIC COMPOUNDS YIELDING POLYFUNCTIONALIZED PYRIDINES IN EXCELLENT YIELD VIA A CYCLOADDITION
  203487. ELIMINATION PROCESS. THE USUALLY HIGH REGIOSELECTIVITY B*AND ITS DEPENDENCE ON THE NATURE OF THE 3
  203488. 15787N
  203489. 2/28/96
  203490. THE SYNTHESIS OF 3
  203491. FUNCTIONALIZED 5
  203492. CHLORO
  203493. METHYL
  203494. OXAZIN
  203495. ONES AND OF PYRIDINES FROM CYCLOADDITION
  203496. ELIMINATION REACTIONS WITH SUBSTITUTED ACETYLENIC COMPOUNDS
  203497. 1994X    5211
  203498. 5224Y
  203499. 14779
  203500. BELLINA, F.
  203501. TetrahedronC
  203502. CARBON BOND FORMATION STEREOSPECIFIC SYNTHESIS CONTROLLED CARBOMETALATION E
  203503. VINYLSTANNANES 
  203504. ALKYNES 
  203505. TRANSMETALATION ELECTROPHILES 
  203506. DERIVATIVES 
  203507. ACETYLENES 
  203508. REAGENTS 
  203509. SEVERAL PROCEDURES, WHICH ARE BASED ON THE ZIRCONIUM
  203510. CATALYZED METHYLALUMINATION OF 1
  203511. ALKYNES (5), HAVE BEEN TESTED FOR THE REGIO
  203512.  AND STEREOSELECTIVE SYNTHESIS OF (E)
  203513. METHYL
  203514. ALKENYLTRIMETHYLSTANNANES (4). THE BEST ONE AMONG THESE PROCEDURES AS REGARDS SIMPLICITY AND MILDNESS IS THAT BASED ON THE WATER
  203515. ACCELERATED METHYLALUMINATION OF COMPOUNDS 5, FOLLOWED BY TREATMENT WITH A THF SOLUTION OF ME3SNCL. THIS PROCEDURE ALLOWS THE PREPARATION OF (E)
  203516. METHYLETHENYLTRIMETHYL STANNES, BJ(E)
  203517. BENZYL
  203518. METHYLETHENYLTRIMETHYLSTANNANES AND (E)
  203519. CYCLOALKENYL)
  203520. 15788N
  203521. 2/28/96
  203522. A_REGIO
  203523.  AND STEREOSELECTIVE SYNTHESIS OF (E)
  203524. METHYL
  203525. ALKENYLTRIMETHYLSTANNANES FROM 1
  203526. ALKYNES
  203527. 1994X    5189
  203528. 5202Y
  203529. 14780
  203530. MILLER, D. J.
  203531. TetrahedronCH1,3
  203532. DIPOLAR CYCLOADDITIONS 2
  203533. (ETHYLTHIO)
  203534. AZETINES CHLORIDES 
  203535. ETHOXY 
  203536. tTHE CYCLOADDITION REACTIONS OF THREE CYCLIC IMIDATE ESTERS, 2
  203537. ETHOXYPYRROLIN
  203538. ONE (6), 2
  203539. ETHOXYISOINDOL
  203540. ONE (7) AND 2
  203541. ETHOXY
  203542. INDOL
  203543. ONE (8) WITH VARIOUS 1,3
  203544. DIPOLES WERE INVESTIGATED. DIPOLAROPHILE 6 ADDED ONLY TO NITRILE OXIDES;  8 ADDED TO NITRILE OXIDES AND TO NITRILIMINES;  7 FAILED TO UNDERGO CYCLOADDITION REACTIONS WITH EITHER NITRILE OXIDES OR NITRILIMINES
  203545. 15789N
  203546. 2/28/96
  203547. A~REACTIONS OF NITRILE OXIDES AND NITRILIMINES WITH IMIDATE ESTERS, THE NITROGEN ATOM OF WHICH FORMS PART OF A HETEROCYCLIC RING
  203548. 1994X    5159
  203549. 5168Y
  203550. 14781
  203551. FOUBELO, F.
  203552. TetrahedronCRC BOND FORMATION VERSATILE 
  203553. REAGENT 
  203554. LITHIUM COMPOUNDS DERIVATIVES 
  203555. ALKENES 
  203556. ACID 
  203557. THE REACTION OF IODOESTERS 1A
  203558. C WITH ELECTROPHILIC OLEFINS 2A
  203559. D AND IN SITU GENERATED TRIBUTYLTIN HYDRIDE (FROM A SUBSTOICHIOMETRIC AMOUNT OF TRIBUTYLTIN CHLORIDE AND AN EXCESS OF SODIUM BOROHYDRIDE) IN THE PRESENCE OF A CATALYTIC AMOUNT OF AIBN IN ETHANOL AT 0 TO 20 
  203560.  C YIELDS THE EXPECTED COUPLING PRODUCTS 3AA
  203561. 3CD. PRODUCTS 4 RESULTING FROM AN IODINE/HYDROGEN EXCHANGE ARE ALSO OBTAINED AS BY
  203562. PRODUCTS IN VARIABLE AMOUNTS. THE STEREOCHEMISTRY OF THE COUPLING REACTION IS STUDIED:   STARTINGB- FROM TRANS
  203563. IODOCYCLOHEXYL ACETATE (1D) AND
  203564. 15790N
  203565. 2/28/96
  203566. FUNCTIONALISED RADICALS IN ORGANIC SYNTHESIS 
  203567. ACYLOXYALKYL RADICALS FROM 2
  203568. ACYLOXYALKYL IODIDES BY THE TIN ROUTE
  203569. 1994X    5131
  203570. 5138Y
  203571. 14782
  203572. ARDILL, H.
  203573. TetrahedronC
  203574. x-RAY CRYSTAL STRUCTURE HETEROCYCLIC COMPOUNDS LATENT 
  203575. FINGERPRINTS 
  203576. ROUTE 
  203577. REARRANGEMENTS CYCLOADDITION 
  203578. GENERATION 
  203579. REACTIVITY 
  203580. ESTERS 
  203581. CYCLIC 5
  203582.  AND 6
  203583. MEMBERED SECONDARY ALPHA
  203584. AMINO ACIDS READ WITH FORMALDEHYDE AND ACETYLENIC DIPOLAROPHILES VIA AZOMETHINE YLIDE FORMATION, CYCLOADDITION AND SUBSEQUENT RING EXPANSION TO GIVE 8
  203585.  AND 9
  203586.  MEMBERED RINGS RESPECTIVELY. RING EXPANSION OCCURS BY REACTION OF THE BRIDGEHEAD NITROGEN OF THE INITIAL BICYCLIC CYCLOADDUCT WITH A FURTHER MOLECULE OF DIPOLAROPHILE TO GIVE A ZWITTERION WHICH TRIGGERS THE RING EXPANSION. DYNAMIC P.M.R. STUDIES SHOW THAT RING INVERSION BETWEEN PAIRS OF MIRRORB4 IMAGE CONFORMATIONS OF THE MEDIUM RING PRODUCTS ARE
  203587. 15791N
  203588. 2/28/96
  203589. ZH SYSTEMS AS POTENTIAL 1,3
  203590. DIPOLES .42. DECARBOXYLATIVE THREE CARBON RING EXPANSION OF CYCLIC SECONDARY A
  203591. AMINO ACIDS VIA AZOMETHINE YLIDE FORMATION
  203592. 1994X    5067
  203593. 5082Y
  203594. 14783
  203595. MOLINA, P.
  203596. TetrahedronC%ONE
  203597. POT PREPARATION ANALOGS 
  203598. INDOLES 
  203599. AN INTRAMOLECULAR DIELS
  203600. ALDER CYCLOADDITION OF thE KETENIMINES 3, AVAILABLE BY AZA WITTIG REACTION BETWEEN IMINOPHOSPHORANES 2, DERIVED FROM AZIDO OLEFINS 1, AND DIARYL KETENES FOLLOWED BY AN OXIDATIVE AROMATIZATION OF THE CYCLOADDUCT PROVIDED BENZ[F]INDOLES 5. ATTEMPTS TO APPLY THIS PROCESS EITHER WITH ETHYLPHENYLKETEN, 5
  203601. PENTENYLAZIDES OR WITH THE RELATED CARBODIIMIDES FAILED
  203602. 15792N
  203603. 2/28/96
  203604. AyA STRAIGHTFORWARD PREPARATION OF BENZ[F]INDOLES BY AN INTRAMOLECULAR DIELS
  203605. ALDER CYCLOADDITION OF UNSATURATED KETENIMINES
  203606. MILLER, R. B.
  203607. Syn. Commun.C    DOPAMINE M
  203608. 15793N
  203609. 2/28/96
  203610. A@AN EFFICIENT SYNTHESIS OF 4
  203611. 1,2,3,4
  203612. TETRAHYDROISOQUINOLINES
  203613. 1994X    1187
  203614. 1193Y
  203615. 14785
  203616. JURGENS, A. R.
  203617. Syn. Commun.C
  203618. LACTAM M
  203619. 15794N
  203620. 2/28/96
  203621. AJPROCESS IMPROVED PREPARATION OF A VERSATILE A
  203622. KETOESTER ACYL ANION SYNTHON
  203623. 1994X    1171
  203624. 1177Y
  203625. 14786
  203626. VENKOV, A. P.
  203627. MOLECULAR DIELS
  203628. ALDER CYCLOADDITION OF thE KETENIMINES 3, AVAILABLE BY AZA WITTIG REACTION BETWEEN IMINOPHOSPHORANES 2, DERIVED FROM AZIDO OLEFINS 1, AND DIARYL KETENES FOLLOWED BY AN OXIDATIVE AROMATIZATION OF THE CYCLOADDUCT PROVIDED BENZ[F]INDOLES 5. ATTEMPTS TO APPLY THIS PROCESS EITHER WITH ETHYLPHENYLKETEN, 5
  203629. PENTENYLAZIDES OR WITH THE RELATED CARBODIIMIDES FAILED
  203630. 15792N
  203631. 2/28/96
  203632. AyA STRAIGHTFORWARD PREPARATION OF BENZ[F]INDOLES BY AN INTRAMOLECULAR DIELS
  203633. ALDER CYCLOADDITION OF UNSATURATED KETENIMINES
  203634. Syn. Commun.M
  203635. 15795N
  203636. 2/28/96
  203637. AZSYNTHESIS OF 3
  203638. DIHYDROISOQUINOLINES FROM ETHYL 2
  203639. ACYLPHENYLACETATES AND FORMAMIDES
  203640. 1994X    1145
  203641. 1150Y
  203642. 14787
  203643. GOURDOUPIS, C. G.
  203644. Syn. Commun.C(CONVENIENT SYNTHESIS AROMATIC
  203645. COMPOUNDS M
  203646. 15796N
  203647. 2/28/96
  203648. THE UTILITY OF THE PUMMERER REARRANGEMENT INTERMEDIATES IN THE PRESENCE OF LEWIS ACIDS 
  203649.  A SHORT AND PRACTICAL SYNTHESIS OF 4
  203650. PROPYLAMINOETHYL)
  203651. METHOXYINDOLE
  203652. 1994X    1137
  203653. 1144Y
  203654. 14788
  203655. A    AHMAN, J.
  203656. Syn. Commun.M
  203657. 15797N
  203658. 2/28/96
  203659. A8AN IMPROVED PROCEDURE FOR THE N
  203660. ALKYLATION OF AZIRIDINES
  203661. 1994X    1121
  203662. 1127Y
  203663. 14789
  203664. Kim, H. R.B
  203665. Syn. Commun.C>DIPOLAR CYCLOADDITIONS TETRAHYDROFURANS CONVERSION 
  203666. FORSKOLIN M
  203667. 15798N
  203668. 2/28/96
  203669. REGIOSELECTIVITY AND STEREOSELECTIVITY IN THE INTRAMOLECULAR NITRILE OXIDE
  203670. OLEFIN CYCLOADDITION (INOC) REACTION AND THE INTRAMOLECULAR SILYL NITRONATE
  203671. OLEFIN CYCLOADDITION (ISOC) REACTION
  203672. 1994X    1107
  203673. 1116Y
  203674. 14790
  203675. ALMENA, I.
  203676. Syn. Commun.
  203677. AJPHASE
  203678. TRANSFER CATALYSIS ORGANIC
  203679. SYNTHESIS IMPROVEMENT 
  203680. ACTIVATION 
  203681. ANION 
  203682. 15799N
  203683. 2/28/96
  203684. A=SELECTIVE ALKYLATION OF 2
  203685. PYRIDONE IN SOLVENT
  203686. FREE CONDITIONS
  203687. 1994X    1057
  203688. 1063Y
  203689. 14791
  203690. SANTHOSH, K. C.
  203691. Syn. Commun.C,DIETHYL AZODICARBOXYLATE TRIPHENYLPHOSPHINE M
  203692. 15800N
  203693. 2/28/96
  203694. AbA FACILE AND STEREOSELECTIVE SYNTHESIS OF ARYLETHERS OF VICINAL BROMOHYDRINS BY MITSUNOBU REACTION
  203695. 1994X    1049
  203696. 1056Y
  203697. 14792
  203698. BRUNET, J. J.
  203699. J. Organomet. Chem.
  203700. RHODIUM 
  203701. NORBORNENE HYDROARYLATION HYDROAMINATION 
  203702. CATALYSIS 
  203703. UNPROTECTED 
  203704. AMINO 
  203705. OLEFINS 
  203706. BOND STRENGTHS 
  203707. AMINATION 
  203708. ALKENES 
  203709. 15801N
  203710. 2/28/96
  203711. AgRHODIUM
  203712. CATALYSED HYDROAMINATION
  203713. HYDROARYLATION OF NORBORNENE WITH ANILINE, TOLUIDINES OR DIPHENYLAMINE
  203714. 1994X
  203715. 14793
  203716. SCHUMANN, H.
  203717. J. Organomet. Chem.
  203718. >C@RHODIUM 
  203719. PHOSPHINE HYDROFORMYLATION 
  203720. RAY DIFFRACTION 
  203721. CRYSTAL M
  203722. 15802N
  203723. 2/28/96
  203724. EFFECTS OF CHANGES IN THE LIGANDS ON THE SKELETON AND THE CATALYTIC ACTIVITY OF SOME NEW RHODIUM COMPLEXES WITH PYRAZOLATO MOIETIES
  203725. 1994X
  203726. 14794
  203727. WESTERHAUSEN, M.
  203728. J. Organomet. Chem.CuSILICON 
  203729. ZINC 
  203730. TRIMETHYLSILYL CRYSTAL
  203731. STRUCTURES MOLECULAR
  203732. STRUCTURE  
  203733. DIMETHYLZINC 
  203734. DIPHENYLZINC 
  203735. COMPLEXES 
  203736. ETHERS M
  203737. 15803N
  203738. 2/28/96
  203739. A>HETEROLEPTIC DIORGANOZINC COMPOUNDS OF THE TYPE (ME3SI)3C
  203740. 1994X
  203741. 14795
  203742. BILLERA, C. F.
  203743. 15804N
  203744. 2/28/96
  203745. ATINTRAMOLECULAR DIYL TRAPPING CHEMISTRY 
  203746.  DIYL
  203747. DECOUPLING AND 7
  203748. TRIG CYCLIZATION
  203749. 1994X    2270
  203750. 2272Y
  203751. 14796
  203752. PEARSON, A. J.
  203753. 15805N
  203754. 2/28/96
  203755. SOME STUDIES ON THE USES OF 2
  203756. BROMOETHYL AND 2
  203757. IODOETHYL ESTER BLOCKING GROUPS IN PEPTIDE SYNTHESIS 
  203758.  SAMARIUM DIIODIDE
  203759. MEDIATED DEPROTECTION
  203760. 1994X    2257
  203761. 2260Y
  203762. 14797
  203763. KRAUS, G. A.
  203764. A!DIELS
  203765. ALDER REACTIONS AKLAVINONE 
  203766. 15806N
  203767. 2/28/96
  203768. ASREGIOCONTROL BY REMOTE SUBSTITUENTS 
  203769.  A DIRECT TOTAL SYNTHESIS OF RACEMIC HONGCONIN
  203770. 1994X    2219
  203771. 2222Y
  203772. 14798
  203773. FUJI, K.
  203774. DIELS
  203775. ALDER REACTIONS HIGH
  203776. PRESSURE ORGANIC
  203777. SYNTHESIS 
  203778. VINYL SULFOXIDES CYCLOPENTADIENE DIENOPHILES 
  203779. CHEMISTRY ENANTIOSELECTIVITY DERIVATIVES 
  203780. REACTIVITYM
  203781. 15807N
  203782. 2/28/96
  203783. AZDIASTEREOSELECTIVE DIELS
  203784. ALDER CYCLOADDITIONS WITH CHIRAL 1
  203785. (ALKYLSULFINYL)
  203786. NITROALKENES
  203787. 1994X    2211
  203788. 2218Y
  203789. 14799
  203790. Rao, C. J.B
  203791. JOCCFTRIPLET NITROGEN MOLECULES ACYLATION 
  203792. ACETONE 
  203793. KETONES 
  203794. STATES 
  203795. ENERGYM
  203796. 15808N
  203797. 2/28/96
  203798. AtSUBSTITUENT EFFECTS ON PHOTOCHEMICAL HYDROGEN ABSTRACTION IN 2
  203799. ACYLPYRIDINES, 2
  203800. ACYLPYRAZINES, AND 4
  203801. ACYLPYRIMIDINES
  203802. 1994X    2125
  203803. 2131Y
  203804. 14800
  203805. MORKEN, P. A.
  203806. REDUCTION 
  203807. FLUOROCARBONS 
  203808. METALM
  203809. 15809N
  203810. 2/28/96
  203811. AlMILD, ZINC
  203812. INDUCED DEFLUORINATION OF BUTATRIENES 
  203813.  STEREOSELECTIVE FORMATION OF DIVINYLACETYLENE DERIVATIVES
  203814. 1994X    2119
  203815. 2121Y
  203816. 14801
  203817. REIN, K. S.
  203818. SENSITIVE SODIUM
  203819. CHANNELS RAT
  203820. BRAIN SYNAPTOSOMES RED TIDE ORGANISM PTYCHODISCUS
  203821. BREVIS GYMNODINIUM
  203822. BREVE CIGUATOXIN TOXIN ASSIGNMENTS 
  203823. JAVANICUS 
  203824. SITESM
  203825. 15810N
  203826. 2/28/96
  203827. AmBREVETOXIN B 
  203828.  CHEMICAL MODIFICATIONS, SYNAPTOSOME BINDING, TOXICITY, AND AN UNEXPECTED CONFORMATIONAL EFFECT
  203829. 1994X    2107
  203830. 2113Y
  203831. 14802
  203832. MARQUART, A. L.
  203833. ENANTIOSELECTIVE SYNTHESIS 
  203834. INDOLIZIDINE ALKALOIDS INTRAMOLECULAR CYCLOADDITION 
  203835. DIPOLAR CYCLOADDITION ASYMMETRIC
  203836. SYNTHESIS (
  203837. SWAINSONINE (+)
  203838. CASTANOSPERMINE CASTANOSPERMINE SWAINSONINE 
  203839. AZIDES M
  203840. 15811N
  203841. 2/28/96
  203842. AnSYNTHESIS OF CHIRAL HYDROXYLATED QUINOLIZIDINES VIA VINYLOGOUS BISCHLER
  203843. NAPIERALSKI NITRILIUM ION CYCLIZATIONS
  203844. 1994X    2092
  203845. 2100Y
  203846. 14803
  203847. PAQUETTE, L. A.
  203848. ORGANO
  203849. LITHIUM COMPOUNDS 
  203850. DIRECTED ORTHO METALATION ASPERGILLUS
  203851. USTUS POLYSUBSTITUTED AROMATICS STRUCTURE ELUCIDATION TERTIARY AMIDES 
  203852. F METABOLITES 
  203853. ETHERS 
  203854. VINYL M
  203855. 15812N
  203856. 2/28/96
  203857. RELEVANCE OF CONFORMATIONAL CONSTRAINTS TO THE REGIOSELECTIVE LITHIATION OF AROMATIC DIETHERS 
  203858.  APPLICATION TO THE CONVENIENT CONSTRUCTION OF THE DEF TRICYCLIC SUBUNIT OF THE AUSTALIDES
  203859. 1994X    2043
  203860. 2051Y
  203861. 14804
  203862. A    DOYON, J.
  203863. COPE REARRANGEMENT CONTROLLED NUCLEOPHILIC ADDITIONS 
  203864. INDACENE SUBUNIT b,g
  203865. UNSATURATED KETONES STEREOCONTROLLED CONSTRUCTION MOLECULAR
  203866. RECOGNITION TRANSITION STRUCTURES CARBONYL
  203867. COMPOUNDS GRIGNARD
  203868. REAGENTS ORGANIC
  203869. REACTIONS 
  203870. 15813N
  203871. 2/28/96
  203872. DIASTEREOSELECTIVITIES ASSOCIATED WITH THE 1,2
  203873. ADDITION OF CHIRAL (RACEMIC) CYCLOPENTENYL ORGANOMETALLICS TO BICYCLO[2.2.2]OCTENONES
  203874. 1994X    2033
  203875. 2042Y
  203876. 14805
  203877. HUVAL, C. C.
  203878. CYCLOADDITION REACTION ATOM TRANSFER 
  203879. ADDITION 
  203880. SUBSTITUTED VINYLCYCLOPROPANES RADICAL ANNULATION REAGENTS 
  203881. CYCLOADDITION 
  203882. ALKENES 
  203883. COMPLEXES 
  203884. STRATEGY M
  203885. 15814N
  203886. 2/28/96
  203887. VERSATILE [3+2] METHYLENECYCLOPENTANE ANNULATIONS OF UNACTIVATED AND ELECTRON
  203888. RICH OLEFINS WITH [(TRIMETHYLSILYL)METHYLENE]CYCLOPROPANEDICARBOXYLATES
  203889. 1994X    2020
  203890. 2024Y
  203891. 14806
  203892. JACOBS, H. K.
  203893. BAKERS
  203894. YEAST REDUCTION b
  203895. KETO SULFONES 
  203896. PHENYL SULFONES 
  203897. ACID 
  203898. C DERIVATIVES HYDROXYSULFONES CYCLIZATION 
  203899. RESOLUTION 
  203900. CHEMISTRY 
  203901. DIANIONS 
  203902. 15815N
  203903. 2/28/96
  203904. FACILE INTRAMOLECULAR ACYLATION REACTIONS OF g
  203905.  AND d
  203906. (ACYLOXY)SULFONES 
  203907.  SYNTHESIS OF SUBSTITUTED CHIRAL DIHYDROFURANS AND DIHYDROPYRANS
  203908. 1994X    2014
  203909. 2019Y
  203910. 14807
  203911. CHOU, S. S. P.
  203912. FACILE SYNTHESIS REGIOSELECTIVE ALKYLATION STEREOSELECTIVE SYNTHESIS ADDITION REACTIONS 
  203913. SULFUR 
  203914. DIENES 
  203915. DIENES 
  203916. BUTADIENES DERIVATIVES TRANSFORMATIONS M
  203917. 15816N
  203918. 2/28/96
  203919. AIINTRAMOLECULAR DIELS
  203920. ALDER REACTIONS VIA SULFONE
  203921. SUBSTITUTED 3
  203922. SULFOLENES
  203923. 1994X    2010
  203924. 2013Y
  203925. 14808
  203926. UDDING, J. H.
  203927. ATOM TRANSFER 
  203928. CYCLIZATION 
  203929. OXACYCLIC 
  203930. CARBOXYLIC ESTERS 
  203931. IODO ESTERS 
  203932. EFFICIENT SYNTHESIS g
  203933. LACTONES 
  203934. ENE REACTION 
  203935. GLYOXYLATE REARRANGEMENT 
  203936. 15817N
  203937. 2/28/96
  203938. TRANSITION METAL
  203939. CATALYZED, CHLORINE
  203940. TRANSFER RADICAL CYCLIZATIONS OF 2
  203941. ALKEN
  203942. CHLOROACETATES 
  203943.  FORMAL TOTAL SYNTHESIS OF AVENACIOLIDE AND ISOAVENACIOLIDE
  203944. 1994X    1993
  203945. 2003Y
  203946. 14809
  203947. PIOTTI, M. E.
  203948. 15818N
  203949. 2/28/96
  203950. REGIOSELECTIVE AND IN SOME CASES STEREOSELECTIVE CARBONYLATION OF A
  203951. ALLENIC ALCOHOLS TO A
  203952. VINYLACRYLIC ACIDS CATALYZED BY A CATIONIC PALLADIUM COMPLEX
  203953. 1994X    1956
  203954. 1957Y
  203955. 14810
  203956. A    AHMAN, J.
  203957. J.C.S. Perkin Trans. 1CKSTEREOCHEMICAL ASPECTS ORGANIC
  203958. SYNTHESIS 
  203959. CHAIN REACTIONS ENAMINES 
  203960. DESIGN M
  203961. 15819N
  203962. 2/28/96
  203963. ATPREPARATION AND INTRAMOLECULAR RADICAL CYCLIZATION OF SOME CYCLIC N
  203964. SULFONYLENAMINES
  203965. 1994X    1079
  203966. 1082Z
  203967. 14811
  203968. BARLUENGA, J.
  203969. J.C.S. Perkin Trans. 1CMONE
  203970. POT SYNTHESIS STEREOSELECTIVE LITHIATION EASY ENTRY 
  203971. AMINES 
  203972. DERIVATIVES M
  203973. 15820N
  203974. 2/28/96
  203975. TRIANIONS BY REGIO
  203976.  AND STEREOSELECTIVE LITHIATION OF DIALLYLAMINES AND STRUCTURALLY RELATED COMPOUNDS 
  203977.  SYNTHETIC APPLICATIONS
  203978. 1994X    1069
  203979. 1077Z
  203980. 14812
  203981. BASSINDALE, A. R.
  203982. J.C.S. Perkin Trans. 1CEORGANIC
  203983. SYNTHESIS 
  203984. CYCLIC SULFATES 
  203985. OLEFINS 
  203986. ALLYLSILANES 
  203987. INDUCTION M
  203988. 15821N
  203989. 2/28/96
  203990. A6ASYMMETRIC DIHYDROXYLATION OF VINYL
  203991.  AND ALLYL
  203992. SILANES
  203993. 1994X    1061
  203994. 1067Z
  203995. 14813
  203996. SHEPHERD, M. K.
  203997. J.C.S. Perkin Trans. 1C>POLYCYCLIC BIPHENYLENES RESONANCE THEORY <3>PHENYLENE SYSTEMS M
  203998. 15822N
  203999. 2/28/96V0CYCLOBUTARENES .4. BIPHENYLENO[2,1
  204000. A]BIPHENYLENEW
  204001. 1994X    1055
  204002. 1059Z
  204003. 14814
  204004. BLOXHAM, J.
  204005. J.C.S. Perkin Trans. 1
  204006. ALPHA,BETA
  204007. UNSATURATED THIONE DIMERS DIELS
  204008. ALDER REACTION 
  204009. CYCLOADDITIONS 2
  204010. ACYLAMINO)
  204011. DIENES 
  204012. GENERATION 
  204013. CHEMISTRY 2
  204014. ARYLIDENE
  204015. THIOTETRALONES 
  204016. CYCLOADDITIONS THIOCHALCONES THIOKETONES 
  204017. 15823N
  204018. 2/28/96
  204019. AmREACTION OF 3
  204020. CYANOTHIOACRYLAMIDES WITH ELECTRON
  204021. DEFICIENT ALKYNES 
  204022.  SYNTHESIS OF 4
  204023. THIOPYRANS
  204024. 1994X
  204025. 14815
  204026. BOA, A. N.
  204027. J.C.S. Perkin Trans. 1
  204028. OPPOLZERS CHIRAL SULTAM DIELS
  204029. ALDER REACTION CYCLOADDITIONS ASYMMETRIC INDUCTION d
  204030. ISOXAZOLINES 5,6
  204031. DIHYDRO
  204032. OXAZINES 
  204033. STEREOCHEMISTRY NITROSOALKENES CONFORMATIONS 1,3
  204034. DIPOLAR 
  204035. 15824N
  204036. 2/28/96
  204037. A:CYCLOADDITION OF NITRILE OXIDES TO HOMOCHIRAL VINYL ETHERS
  204038. 1994X
  204039. 14816
  204040. BOHN, T.
  204041. J.C.S. Perkin Trans. 1C7(VINYLIMINO)PHOSPHORANES RING 
  204042. CYCLOADDITION 
  204043. PYRIDINE M
  204044. 15825N
  204045. 2/28/96
  204046. A^SYNTHESIS OF 1,6
  204047. METHANO[10]ANNULENOPYRIDINES BY TANDEM AZA
  204048. WITTIG REACTION/ELECTROCYCLISATION
  204049. 1994X
  204050. 14817
  204051. RANU, B. C.
  204052. J.C.S. Perkin Trans. 1C
  204053. CATALYZED REARRANGEMENT 
  204054. RETROALDOL 
  204055. CLEAVAGE STEREOCONTROLLED CONSTRUCTION ORGANIC
  204056. SYNTHESIS CYCLOHEPTANOIDS PHOTOADDUCTS 
  204057. EFFICIENT SYSTEMS M
  204058. 15826N
  204059. 2/28/96
  204060. AOTWO
  204061. CARBON RING EXPANSION THROUGH FREE CYCLOBUTYLCARBINYL RADICAL FRAGMENTATION
  204062. 1994X
  204063. 14818
  204064. GROMOV, S. P.
  204065. HeterocyclesM
  204066. 15827N
  204067. 2/28/96V
  204068. ENAMINE REARRANGEMENTW
  204069. 1994X    1127
  204070. 1155Y
  204071. 14819
  204072. STAJER, G.
  204073. HeterocyclesC
  204074. NORBORNENE 
  204075. HETEROCYCLES M
  204076. 15828N
  204077. 2/28/96
  204078. AbPREPARATION AND STERIC STRUCTURE OF CONDENSED
  204079. SKELETON SATURATED DIPHENYL
  204080. SUBSTITUTED ISOINDOLONES
  204081. 1994X    1061
  204082. 1070Y
  204083. 14820
  204084. KATRITZKY, A. R.
  204085. HeterocyclesM
  204086. 15829N
  204087. 2/28/96
  204088. ALTHE DIVERSE REACTIVITY OF (BENZOTHIAZOL
  204089. YLTHIO)
  204090. (BENZOTRIAZOL
  204091. YL)METHANE
  204092. 1994X    1041
  204093. 1052Y
  204094. 14821
  204095. IWAKAWA, T.
  204096. HeterocyclesC
  204097. DIOXIDESM
  204098. 15830N
  204099. 2/28/96
  204100. CYCLOADDITION IN SYNTHESIS OF SULFONAMIDE DERIVATIVES .6. UNEXPECTED PRODUCTS FROM THE REACTION OF DITHIOCARBAMATE WITH CHLOROSULFONYL ISOCYANATE 
  204101.  A NOVEL SYNTHETIC ROUTE TO 5
  204102. AMINO
  204103. 1,2,4
  204104. DITHIAZOL
  204105. ONE AND N,N
  204106. DISUBSTITUTED N'
  204107. CHLOROSULFONYLCARBAMIMIDOYL CHLORIDE
  204108. 1994X    1015
  204109. 1024Y
  204110. 14822
  204111. HUSSEIN, A. Q.
  204112. Heterocycles
  204113. AMINO
  204114. 1,2,4
  204115. OXADIAZOLINES 1,3,4
  204116. OXADIAZOLES 
  204117. 15831N
  204118. 2/28/96
  204119. RING TRANSFORMATION OF HETEROCYCLES .3. A CONVERSION OF 4
  204120. AMINO
  204121. 1,2,4
  204122. OXADIAZOLINES INTO 2
  204123. ARYLAMINO
  204124. 1,3,4
  204125. THIADIAZOLES AND OXA
  204126. ANALOGUES
  204127. 1994X
  204128. 14823
  204129. SUZUKI, T.
  204130. HeterocyclesM
  204131. 15832N
  204132. 2/28/96
  204133. AuHIGH
  204134. PRESSURE INTERMOLECULAR DIELS
  204135. ALDER REACTIONS OF THE NOVEL BUILDING BLOCK 
  204136.  4H,6H
  204137. THIENO[3,4
  204138. C]FURAN 5,5
  204139. DIOXIDE
  204140. 1994X
  204141. 14824
  204142. KAKUSAWA, N.
  204143. HeterocyclesM
  204144. 15833N
  204145. 2/28/96
  204146. A7SYNTHESIS AND REACTIONS OF NOVEL TROPONO[4,5
  204147. B]OXEPINES
  204148. 1994X
  204149. 14825
  204150. MEKHEIMER, R.
  204151. J. Chem. Res.
  204152. 15834N
  204153. 2/28/96
  204154. A.UNUSUAL REACTION OF NITRONES WITH OXO
  204155. DIAZOLES
  204156. 1994X
  204157. 14826
  204158. CHAN, W. H.
  204159. J. Chem. Res.
  204160. SC9VINYL SULFOXIDE CYCLOADDITIONS EQUIVALENTS CYCLOADDITIONSM
  204161. 15835N
  204162. 2/28/96
  204163. ABACETYLENIC SULFINATES IN ORGANIC SYNTHESIS 
  204164.  DIELS
  204165. ALDER REACTIONS
  204166. 1994X
  204167. 14827
  204168. MOHAREB, R. M.
  204169. J. Chem. Res.
  204170. 15836N
  204171. 2/28/96
  204172. THE REACTION OF ACTIVE METHYLENE REAGENTS WITH SULFUR AND PHENYL ISOTHIOCYANATE 
  204173.  NOVEL SYNTHESIS OF THIAZOLE, THIAZOLO[4,5
  204174. D]PYRIMIDINE AND 4,5'
  204175. BITHIAZOLYL DERIVATIVES
  204176. 1994X
  204177. 14828
  204178. CARDIN, C. J.
  204179. J. Chem. Res.
  204180. 15837N
  204181. 2/28/96
  204182. A;SYNTHESIS OF THE TRICYCLO[6.2.1.03,8]UNDECAN
  204183. ONE SKELETON
  204184. 1994X
  204185. 14829
  204186. FLEMING, P. E.
  204187. JACSM
  204188. 15838N
  204189. 2/28/96
  204190. ADBIOSYNTHESIS OF TAXOIDS 
  204191.  MODE OF ATTACHMENT OF THE TAXOL SIDE CHAIN
  204192. 1994X    4137
  204193. 4138Y
  204194. 14830
  204195. MARUOKA, K.
  204196. JACSM
  204197. 15839N
  204198. 2/28/96
  204199. A{VIRTUALLY COMPLETE BLOCKING OF A,b
  204200. UNSATURATED ALDEHYDE CARBONYLS BY COMPLEXATION WITH ALUMINUM TRIS(2,6
  204201. DIPHENYLPHENOXIDE)
  204202. 1994X    4131
  204203. 4132Y
  204204. 14831
  204205. TROST, B. M.
  204206. JACSM
  204207. 15840N
  204208. 2/28/96
  204209. AFASYMMETRIC INDUCTION IN ALLYLIC ALKYLATIONS OF 3
  204210. (ACYLOXY)CYCLOALKENES
  204211. 1994X    4089
  204212. 4090Y
  204213. 14832
  204214. KOBAYASHI, S.
  204215. JACSM
  204216. 15841N
  204217. 2/28/96
  204218. LANTHANIDE(III)
  204219. CATALYZED ENANTIOSELECTIVE DIELS
  204220. ALDER REACTIONS 
  204221.  STEREOSELECTIVE SYNTHESIS OF BOTH ENANTIOMERS BY USING A SINGLE CHIRAL SOURCE AND A CHOICE OF ACHIRAL LIGANDS
  204222. 1994X    4083
  204223. 4084Y
  204224. 14833
  204225. ENGEL, P. S.
  204226. JACSM
  204227. 15842N
  204228. 2/28/96
  204229. A=1,2
  204230. AZOXY REARRANGEMENT AND FRAGMENTATION OF b
  204231. AZOXY RADICALS
  204232. 1994X    4079
  204233. 4080Y
  204234. 14834
  204235. MIKAMI, K.
  204236. JACSM
  204237. 15843N
  204238. 2/28/96
  204239. AxASYMMETRIC CATALYTIC ALDOL
  204240. TYPE REACTION WITH KETENE SILYL ACETALS 
  204241.  POSSIBLE INTERVENTION OF THE SILATROPIC ENE PATHWAY
  204242. 1994X    4077
  204243. 4078Y
  204244. 14835
  204245. ARMSTRONG, B. M.
  204246. JACSM
  204247. 15844N
  204248. 2/28/96
  204249. CARBON ATOM ROUTES TO NITRENES
  204250. 1994X    4071
  204251. 4072Y
  204252. 14836
  204253. BREUTEL, C.
  204254. JACSM
  204255. 15845N
  204256. 2/28/96
  204257. A[AN UNUSUAL, SELECTIVE h(3)
  204258. h(1) ALLYL ISOMERIZATION IN A CHIRAL ALLYLIC ALKYLATION CATALYST
  204259. 1994X    4067
  204260. 4068Y
  204261. 14837
  204262. PALOMA, L. G.
  204263. A{MINOR GROOVE MAGNETIC
  204264. RESONANCE NUCLEIC
  204265. ACIDS 
  204266. COMPLEX 
  204267. PROTEINS 
  204268. (GCATTAATGC)2 ASSIGNMENTS 
  204269. DISTAMYCIN 
  204270. RESOLUTION 
  204271. 15846N
  204272. 2/28/96
  204273. A~INTERACTION OF CALICHEAMICIN WITH DUPLEX DNA 
  204274.  ROLE OF THE OLIGOSACCHARIDE DOMAIN AND IDENTIFICATION OF MULTIPLE BINDING MODES
  204275. 1994X    3697
  204276. 3708Y
  204277. 14838
  204278. MORKVED, E. H.
  204279. Acta Chem. Scand.M
  204280. 15847N
  204281. 2/28/96
  204282. A1REACTIONS OF 1,2,5
  204283. THIADIAZOLE
  204284. DICARBONITRILE
  204285. 1994X
  204286. 14839
  204287. LUDWIG, C.
  204288. Acta Chem. Scand.C
  204289. ENANTIOSELECTIVE SYNTHESIS ANODIC
  204290. OXIDATION L
  204291. LYSINE 
  204292. ELECTROORGANIC CHEMISTRY PYRROLIDINES 
  204293. PIPERIDINES 
  204294. ALKALOIDS 
  204295. PRECURSOR 
  204296. CARBON M
  204297. 15848N
  204298. 2/28/96
  204299. ANSTEREOSELECTIVE ADDITION OF ORGANOCOPPER REAGENTS TO CYCLIC N
  204300. ACYLIMINIUM IONS
  204301. 1994X
  204302. 14840
  204303. Lee, J.B
  204304. Tet. Lett.K
  204305. (VOL 34, PG 415, 1993)M
  204306. 15849N
  204307. 2/28/96
  204308. FLUORINATED VINYL CARBAMATES AND CARBAMOYLOXY ALLYLSILANES, A
  204309. METALATION, ORGANOLITHIUM ADDITION
  204310. ELIMINATION, AND FLUORIDE
  204311. MEDIATED ELECTROPHILIC REACTIVITY PATTERNS 
  204312. 1994X
  204313. 2438Y
  204314. 14841
  204315. DEROOSE, F. D.
  204316. Tet. Lett.C
  204317. BIOTIN 
  204318. CYCLOADDITION 
  204319. A CONCEPTUALLY ATTRACTIVE ENANTIOSELECTIVE 12
  204320. STEP SYNTHESIS OF BIOTIN FROM L
  204321. CYSTEINE IS REPORTED BASED UPON AN INTRAMOLECULAR 1,3
  204322. DIPOLAR CYCLOADDITION SEQUENCE INVOLVING AS KEY
  204323. STEPS (I) THE MACROTHIOLACTONISATION OF ACID 3 TO Z
  204324. OLEFIN 4, (II) THE THERMOLYSIS OF THE ENE CARBAMOYL AZIDE 5 IN WATER WITH DIRECT FORMATION OF A MIXTURE OF THE BENZYLATED DERIVATIVES OF (+)
  204325. BIOTIN 6A AND 6B.
  204326. 15850N
  204327. 2/28/96
  204328. A,A NOVEL ENANTIOSELECTIVE SYNTHESIS OF BIOTIN
  204329. 1994X    2615
  204330. 2618Y
  204331. 14842
  204332. ANDERSSON, P. G.
  204333. Tet. Lett.C
  204334. CARBONYL
  204335. COMPOUNDS TITANIUM 
  204336. IN CONTRAST TO PREVIOUS REPORTS, THE MCMURRY COUPLING REACTION OF ACETOPHENONE HAS BEEN SHOWN TO GIVE PREDOMINANTLY Z
  204337. DIPHENYL
  204338. BUTENE.
  204339. 15851N
  204340. 2/28/96
  204341. AXON THE STEREOCHEMICAL OUTCOME OF THE MCMURRY COUPLING OF ACETOPHENONE, A REINVESTIGATION
  204342. 1994X    2609
  204343. 2610Y
  204344. 14843
  204345. BOTO, A.
  204346. Tet. Lett.C)INTRAMOLECULAR FUNCTIONALIZATION 
  204347. TANDEM 
  204348. THE ALKOXY RADICALS FORMED BY THE REACTION OF STEROIDAL CYCLIC HYDROXYKETONES (1) AND (2) WITH (DIACETOXYIODO)BENZENE AND IODINE OR MERCURIC OXIDE AND IODINE UNDER OXYGEN ATMOSPHERE AND IRRADIATION WITH VISIBLE LIGHT UNDERGO A NEW QUINTUPLE SEQUENCE B
  204349. FRAGMENTATION
  204350. PEROXIDATION
  204351. RADICAL REDUCTION
  204352. RADICAL REDUCTION
  204353. RADICAL CYCLIZATION
  204354. FRAGMENTATION REACTION BEFORE BEING TRAPPED BY AN ATOM OF IODINE.
  204355. 15852N
  204356. 2/28/96
  204357. AAA NEW SEQUENTIAL ALKOXY RADICAL FRAGMENTATION OF d
  204358. HYDROXYKETONES
  204359. 1994X    2597
  204360. 2600Y
  204361. 14844
  204362. CHEN, L. G.
  204363. Tet. Lett.
  204364. ALKENE ADDITION
  204365. REACTIONS 
  204366. ACYL RADICALS 
  204367. HEPTENOYL RADICALS STEREO
  204368. SELECTIVITY REGIO
  204369. SELECTIVITY ORGANIC
  204370. SYNTHESIS 
  204371. CHAIN REACTIONS CYCLIZATIONS 
  204372. TANDEM 
  204373. CARBONYL 
  204374. iTREATMENT OF APPROPRIATELY SUBSTITUTED 5,9
  204375. DIENE, 5,9,13
  204376. TRIENE AND 5,9,13,17
  204377. TETRAENE PHENOSELENYL ESTERS, E.G. 1A, 9 AND 14, WITH BU3SNH
  204378. AIBN IS SHOWN TO LEAD TO LINEAR AND ANGULAR SIX
  204379. RING FUSED POLYCYCLES, VIZ 2, 11 AND 15 RESPECTIVELY, VIA CONSECUTIVE 6
  204380. TRIG MODES OF CYCLISATIONS STARTING FROM THE CORRESPONDING POLYOLEFIN ACYL RADICAL INTERMEDIATES.
  204381. 15853N
  204382. 2/28/96VTNEW RADICAL MEDIATED POLYOLEFIN CYCLISATIONS DIRECTED TOWARDS STEROID RING SYNTHESISW
  204383. 1994X    2593
  204384. 2596Y
  204385. 14845
  204386. ASOKAN, C. V.
  204387. Tet. Lett.
  204388. DITHIOACETALS 
  204389. AN EXPEDIENT AND GENERAL METHOD FOR THE SYNTHESIS OF B
  204390. ALKYLTHIOETHYLENIC ALDEHYDES FROM DITHIOKETALS UNDER VILSMEIER
  204391. HAACK REACTION CONDITIONS IS DESCRIBED.
  204392. 15854N
  204393. 2/28/96
  204394. A|THE VILSMEIER REACTION ON DITHIOKETALS 
  204395.  A FACILE METHOD FOR THE STEREOSELECTIVE SYNTHESIS OF b
  204396. ALKYLTHIOETHYLENIC ALDEHYDES
  204397. 1994X    2585
  204398. 2586Y
  204399. 14846
  204400. A    IBATA, T.
  204401. Tet. Lett.C7KETOHYDRAZONE 
  204402. CU(ACAC)2
  204403. OXIDATION 
  204404. DIAZOKETONE 
  204405. AZINE 
  204406. AN EFFICIENT CU(ACAC)2
  204407. CATALYZED OXIDATION OF KETOHYDRAZONES AFFORDED THE CORRESPONDING A
  204408. DIAZOKETONES OR KETAZINES IN HIGH YIELDS DEPENDING ON THE REACTION CONDITIONS. HOWEVER, THE REACTION OF BENZOPHENONE HYDRAZONE GAVE BENZOPHENONE AZINE WITHOUT AFFORDING DIPHENYLDIAZOMETHANE. THE FORMATION OF AZINES IS EXPLAINED BY THE INTERMEDIACY OF CARBENOID GENERATED BY THE CU(ACAC)2
  204409. CATALYZED DECOMPOSITION OF DIAZO COMPOUNDS.
  204410. 15855N
  204411. 2/28/96
  204412. AjFORMATION OF DIAZOKETONES AND AZINES BY IMPROVED OXIDATION OF KETOHYDRAZONES USING CU(ACAC)2 AS A CATALYST
  204413. 1994X    2581
  204414. 2584Y
  204415. 14847
  204416. KITA, Y.
  204417. Tet. Lett.C
  204418. ACETIC
  204419. ANHYDRIDE CHEMISTRY 
  204420.  THE PUMMERER REACTION OF ACYCLIC SULFOXIDES WITH O
  204421. SILYLATED KETENE ACETAL HAS BEEN SHOWN TO PROCEED WITH HIGH DIASTEREOSELECTIVE DEPROTONATION OF THE A
  204422. METHYLENE PROTON. A PLAUSIBLE REACTION MECHANISM INVOLVING THE ANTI ELIMINATION PROCESS IS PROPOSED FROM DEUTERIUM
  204423. LABELING EXPERIMENT.
  204424. 15856N
  204425. 2/28/96
  204426. AdMECHANISTIC STUDIES OF PUMMERER REACTION IN ACYCLIC SULFOXIDES INDUCED BY O
  204427. SILYLATED KETENE ACETALS
  204428. 1994X    2569
  204429. 2572Y
  204430. 14848
  204431. DESMAELE, D.
  204432. Tet. Lett.
  204433. ANNULATION 
  204434. TANDEM ALKYLATION 
  204435. MICHAEL ADDITION ACTIVE
  204436. MICHAEL ADDITION ACTIVE
  204437. METHYLENE COMPOUNDS CESIUM
  204438. CARBONATE DIELS
  204439. ALDER 
  204440. MALONIC ESTERS, b
  204441. ESTER AND OTHER METHYLENE
  204442. ACTIVE COMPOUNDS REACT WITH THE 7
  204443. HEPTENOIC ACID METHYL ESTER 2 IN PRESENCE OF CESIUM CARBONATE TO GIVE SIX
  204444. MEMBERED RING PRODUCTS 5, THROUGH A TANDEM ALKYLATION
  204445. MICHAEL ADDITION REACTION.
  204446. 15857N
  204447. 2/28/96
  204448. AUCONVENIENT ANNULATION PROCESS INVOLVING A TANDEM ALKYLATION
  204449. MICHAEL ADDITION SEQUENCE
  204450. 1994X    2549
  204451. 2552Y
  204452. 14849
  204453. VANDEWEGHE, P.
  204454. Tet. Lett.C
  204455. ORGANIC
  204456. SYNTHESIS 
  204457. SMI2 PRESENTS CATALYTIC ACTIVITY FOR DIELS
  204458. ALDER REACTIONS BETWEEN CYCLOPENTADIENE OR ISOPRENE AND VARIOUS DIENOPHILES, AND FOR HETERO DIELS
  204459. ALDER REACTIONS.
  204460. 15858N
  204461. 2/28/96
  204462. AUDIIODOSAMARIUM, A CATALYST PRECURSOR FOR DIELS
  204463. ALDER AND HETERO DIELS
  204464. ALDER REACTIONS
  204465. 1994X    2545
  204466. 2548Y
  204467. 14850
  204468. CRANDALL, J. K.
  204469. Tet. Lett.C3PRIMARY AMINES 
  204470. DIOXIRANES 
  204471. EPOXIDATION 
  204472. CHEMISTRY 
  204473. THE DIMETHYLDIOXIRANE OXIDATIONS OF ALLENIC AMINE DERIVATIVES GIVE HIGHLY FUNCTIONALIZED NITROGEN HETEROCYCLES DERIVED FROM CYCLIZATIONS OF INTERMEDIATE ALLENE MONO
  204474.  AND DIEPOXIDES.
  204475. 15859N
  204476. 2/28/96
  204477. AEOXIDATIVE CYCLIZATIONS OF ALLENIC SULFONAMIDES WITH DIMETHYLDIOXIRANE
  204478. 1994X    2513
  204479. 2516Y
  204480. 14851
  204481. MEYERS, A. I.
  204482. Tet. Lett.C
  204483. ALKYL RADICALS 
  204484. OXAZOLINES ARE READILY OXIDIZED TO 1,3
  204485. OXAZOLES USING NBS/PEROXIDE OR LIGHT OR, MORE EFFICIENTLY, BY THE KHARASCH
  204486. SOSNOVSKY REACTION.
  204487. 15860N
  204488. 2/28/96
  204489. A-THE OXIDATION OF 2
  204490. OXAZOLINES TO 1,3
  204491. OXAZOLES
  204492. 1994X    2481
  204493. 2484Y
  204494. 14852
  204495. AGUILAR, E.
  204496. Tet. Lett.C
  204497. TOXIC CYCLIC PEPTIDE BIOLOGICALLY
  204498. ACTIVE CYCLOPEPTIDES AMINO
  204499. ACIDS ORGANIC
  204500. SYNTHESIS 2
  204501. AMINOALKYL)THIAZOLE
  204502. CARBOXYLIC ACIDS STRUCTURAL BIOCHEMISTRY ANTINEOPLASTIC AGENTS PROPOSED STRUCTURE MARINE SPONGE DOLASTATIN
  204503. A RECENTLY REPORTED MODIFIED HANTZSCH REACTION WAS REINVESTIGATED AND CONDITIONS WERE FOUND TO REACH ENANTIOMERICALLY PURE THIAZOLE AMINO ACID DERIVATIVES.
  204504. 15861N
  204505. 2/28/96
  204506. A9REINVESTIGATION OF A MODIFIED HANTZSCH THIAZOLE SYNTHESIS
  204507. 1994X    2473
  204508. 2476Y
  204509. 14853
  204510. A    CRICH, D.
  204511. Tet. Lett.CHBROMINATIVE CYCLIZATIONS SYSTEM 
  204512. DERIVATIVES 
  204513. STRATEGY 
  204514. KETONES 
  204515. HALIDES
  204516. A TAXOL A RING
  204517. SYNTHON IS OBTAINED BY OXIDATIVE CYCLIZATION OF HOMOGERANIC ACID WITH MERCURIC TRIFLATE FOLLOWED BY OXIDATIVE DEMERCURATION; THE MEYER
  204518. SCHUSTER REARRANGEMENT IS THEN EMPLOYED TO FORM THE HIGHLY STERICALLY HINDERED TAXOL 1,2
  204519. BOND.
  204520. 15862N
  204521. 2/28/96
  204522. AkCONCISE SYNTHESIS OF A TAXOL A
  204523. RING SYNTHON 
  204524.  FORMATION OF A 1,2
  204525. ALKYLIDENE LINKAGE VIA ACETYLENE CHEMISTRY
  204526. 1994X    2469
  204527. 2472Y
  204528. 14854
  204529. A    BARRY, J.
  204530. Tet. Lett.CVASYMMETRIC CYCLOPROPANATION EPOXIDATIONS HYDROCARBONS 
  204531. COMPLEXES 
  204532. OXIDATION 
  204533. REAGENTS 
  204534. A NEW SYNTHESIS OF D
  204535. SYMMETRIC PORPHYRINS IS PRESENTED WHICH PROVIDES CHIRAL MACROCYCLES IN ONLY FIVE STEPS STARTING FROM OPTICALLY ACTIVE CYCLIC KETONES. THE EFFICACY OF THIS APPROACH IS DEMONSTRATED WITH THE SYNTHESIS OF A NEW PORPHYRIN DERIVED FROM R
  204536. NOPINONE. THE DEVELOPMENT OF THIS FLEXIBLE AND GENERAL ROUTE SHOULD SPEED THE DEVELOPMENT OF PORPHYRIN
  204537. BASED ASYMMETRIC CATALYSTS.
  204538. 15863N
  204539. 2/28/96
  204540. AbA NEW 5+1 ROUTE TO ARENES 
  204541.  APPLICATION TO THE FACILE SYNTHESIS OF D
  204542. SYMMETRIC CHIRAL PORPHYRINS
  204543. 1994X    2465
  204544. 2468Y
  204545. 14855
  204546. CLIVE, D. L. J.
  204547. Tet. Lett.C&ACYL CYANIDES 
  204548. DERIVATIVES 
  204549. CHEMISTRY 
  204550. METHOXY ACRYLONITRILES, AVAILABLE FROM ALDEHYDES AND KETONES, REACT WITH SODIUM AZIDE IN THE PRESENCE OF cERIc AMMONIUM NITRATE TO GIVE AZIDO NITRATES; FROM THESE COMPOUNDS, A
  204551. AMINO ACIDS ARE OBTAINED BY SEQUENTIAL TREATMENT WITH SODIUM ACETATE IN ACETIC ACID AND THEN METHANOLIC POTASSIUM CARBONATE, FOLLOWED BY HYDROGENATION.
  204552. 15864N
  204553. 2/28/96
  204554. SYNTHESIS OF A
  204555. AMINO ACIDS BY ADDITION OF PUTATIVE AZIDO RADICALS TO A
  204556. METHOXY ACRYLONITRILES DERIVED FROM ALDEHYDES AND KETONES
  204557. 1994X    2459
  204558. 2462Y
  204559. 14856
  204560. ELGENDY, S.
  204561. Tet. Lett.
  204562. THE HYDROBORATION OF 1
  204563. ALKENES BY CATECHOLBORANE IS ACCELERATED BY CATALYTIC AMOUNT OF WILKINSON'S CATALYST RHCL(PPH3)3 TO GIVE A
  204564. HALO BORONIC ESTERS IN GOOD YIELDS.
  204565. 15865N
  204566. 2/28/96
  204567. A6RHODIUM(I)
  204568. CATALYSED HYDROBORATION OF 1
  204569. ALKENES
  204570. 1994X    2435
  204571. 2436Y
  204572. 14857
  204573. HARRIS, M. C. J.
  204574. Tet. Lett.M
  204575. 15866N
  204576. 2/28/96
  204577. AVA PRACTICAL PROCEDURE FOR THE ELABORATION OF AMINES VIA ZIRCONOCENE h2
  204578. IMINE COMPLEXES
  204579. 1994X    2431
  204580. 2434Y
  204581. 14858
  204582. CASIRAGHI, G.
  204583. Tet. Lett.
  204584. CARBAMOYLPOLYOXAMIC ACID DERIVATIVES 
  204585. AN EFFICIENT STEREOSELECTIVE ROUTE TO POLYHYDROXY
  204586. AMINO ACIDS 7A
  204587. F WAS DEVELOPED BY EXPLOITING N
  204588. BUTOXYCARBONYL
  204589.  (TERT
  204590. BUTYLDIMETHYLSILOXY)PYRROLE AS A GLYCINE ANION EQUIVALENT.
  204591. 15867N
  204592. 2/28/96
  204593. BUTOXYCARBONYL
  204594. BUTYLDIMETHYLSILOXY)PYRROLE AS A GLYCINE ANION EQUIVALENT 
  204595.  A FLEXIBLE ENANTIOSELECTIVE ACCESS TO POLYHYDROXY
  204596. AMINO ACIDS
  204597. 1994X    2423
  204598. 2426Y
  204599. 14859
  204600. BEGLEY, M. J.
  204601. Tet. Lett.
  204602. TREATMENT OF THE IODOTRIENONE 1 WITH BU3SNH
  204603. AIBN RESULTS IN THE FORMATION OF THE ANGULAR 5,7,5
  204604. RING FUSED TRICYCLE 6, BY WAY OF A NOVEL SEQUENTIAL 13
  204605. TRIG MACROCYCLISATION FOLLOWED BY TWO SUCCESSIVE 5
  204606. TRIG TRANSANNULATION PROCESSES.
  204607. 15868N
  204608. 2/28/96
  204609. ANA CASCADE MACROCYCLISATION
  204610. TRANSANNULATION APPROACH TO POLYCYCLE CONSTRUCTIONS
  204611. 1994X    2417
  204612. 2420Y
  204613. 14860
  204614. PATTENDEN, G.
  204615. Tet. Lett.C!MACROCYCLIZATION (
  204616. ZEARALENONE 
  204617. DTHE SCOPE FOR TANDEM RADICAL MEDIATED MACROCYCLISATION
  204618.  TRANSANNULATION PROCESSES (SCHEME 1) IN THE ELABORATION OF POLYCYCLES IS ILLUSTRATED WITH THE FACILE SYNTHESES OF LINEAR 5,6
  204619. , 6,6
  204620.  AND 5,7
  204621. RING FUSED CARBOBICYCLES, VIZ 7, 8, 11, 13 FROM APPROPRIATE IODODIENONE PRECURSORS, VIZ 1, 2, 12, ON TREATMENT WITH BU3SNH
  204622. AIBN.
  204623. 15869N
  204624. 2/28/96
  204625. ASSEQUENTIAL RADICAL MACROCYCLISATION
  204626. TRANSANNULATION APPROACH TO RING
  204627. FUSED BICYCLES
  204628. 1994X    2413
  204629. 2416Y
  204630. 14861
  204631. CIATTINI, P. G.
  204632. Tet. Lett.
  204633. HASSNER, A.
  204634. Tet. Lett.OARYL TRIFLATES AND HALIDES (1) PROVIDES A GENERAL AND EFFICIENT METHOD FOR THE SYNTHESIS OF 3
  204635. SUBSTITUTED INDOLES 3.
  204636. 15870N
  204637. 2/28/96
  204638. EFFICIENT SYNTHESIS OF 3
  204639. SUBSTITUTED INDOLES BY PALLADIUM CATALYZED COUPLING REACTION OF 3
  204640. TRIBUTYLSTANNYLINDOLES WITH ORGANIC TRIFLATES AND HALIDES
  204641. 1994X    2405
  204642. 2408Y
  204643. 14862
  204644. HASSNER, A.
  204645. Tet. Lett.
  204646. C)AZOMETHINE 
  204647. YLIDES 
  204648. GLYCOSIDASES 
  204649. POTENT 
  204650. aA NEW ROUTE FOR ASYMMETRIC AZA
  204651. SUGAR ANALOGS STARTING WITH L
  204652. SERINE AND UTILIZING AN INTRAMOLECULAR OXIME OLEFIN CYCLOADDITION HAS BEEN SUCCESSFULLY DEVELOPED. A MEMBER OF THIS FAMILY OF BRANCHED CHAIN SUGAR AMINO DI(HYDROXYMETHYL) PYRROLIDINES (1 AND 2) EXHIBITS SELECTIVE INHIBITION OF A
  204653. GLUCOSIDASE, WHILE NO INHIBITION OF B
  204654. GLUCOSIDASE WAS DETECTED.
  204655. 15871N
  204656. 2/28/96
  204657. UTILIZATION OF L
  204658. SERINE IN AN OXIME OLEFIN CYCLOADDITION ROUTE TO A FUNCTIONALIZED ASYMMETRIC PYRROLIDINE, A SELECTIVE A
  204659. GLUCOSIDASE INHIBITOR
  204660. 1994X    2397
  204661. 2400Y
  204662. 14863
  204663. WARRENER, R. N.
  204664. Tet. Lett.C(DIELS
  204665. ALDER REACTION LEWIS
  204666. ACIDS 
  204667. FURAN 
  204668. THE ENDO,ENDO
  204669. DIBROMO
  204670. OXANORBORNENO 2,3
  204671. C SUCCINIMIDE (1) UNDERGOES COMPLETE INVERSION UPON HYDROGENOLYSIS OF THE BROMINE SUBSTITUENTS TO FORM (5)(ZN/AG COUPLE IN THF) OR (26)(H2, PD/C). THE HIGHLY REACTIVE DIENOPHILE, N
  204672. METHYL 7
  204673. OXANORBORNADIENO 2,3
  204674. C MALEIMIDE (3) IS SHOWN TO BE A TRANSIENT INTERMEDIATES IN THE ZN/AG COUPLE EXPERIMENTS BY TRAPPING WITH FURAN. DEUTERIUM LABELLING EXPERIMENTS HAVE BEEN USED TO HELP ELUCIDATE THE MECHANISM OF THESE REACTIONS.
  204675. 15872N
  204676. 2/28/96
  204677. EVIDENCE FOR AN OLEFINIC INTERMEDIATE IN THE CONFIGURATIONAL INVERSION ACCOMPANYING HYDROGENOLYSIS OF A 7
  204678. OXANORBORNYL VICINAL DIBROMIDE
  204679. 1994X    2389
  204680. 2392Y
  204681. 14864
  204682. FERNANDEZ, E.
  204683. Tet. Lett.
  204684. ADASYMMETRIC HYDROFORMYLATION 
  204685. TIN(II) CHLORIDE 
  204686. LIGANDS 
  204687. MILD 
  204688. VINYL 
  204689. EFFICIENT CONVERSION OF ALKENES TO ACETALS HAS BEEN ACHIEVED BY CONSECUTIVE HYDROFORMYLATION
  204690. ACETALIZATION REACTIONS CATALYZED BY RHODIUM COMPLEXES AND PYRIDINIUM P
  204691. TOLUENESULPHONATE OR BY A ZWITTERIONIC RHODIUM CATALYST.
  204692. 15873
  204693. 2/28/96
  204694. SYNTHESIS OF ACETALS FROM ALKENES BY ONE
  204695. POT HYDROFORMYLATION
  204696. TRANSACETALIZATION REACTIONS CATALYSED BY RHODIUM COMPLEXES AND PYRIDINIUM P
  204697. TOLUENESULPHONATE
  204698. 1994X    2361
  204699. 2364Y
  204700. 14865
  204701. KANG, S. K.
  204702. Tet. Lett.C
  204703. ALKYLATION 
  204704. COMPLEX 
  204705. REACTION OF CHIRAL ALLYLIC AND DIENYLIC CYCLIC CARBONATES WITH VARIOUS NUCLEOPHILES IN THE PRESENCE OF (PPH3)4PD AS A CATALYST AFFORDED A
  204706. , OR E
  204707. SUBSTITUTED PRODUCTS WITH HIGH REGIO
  204708. , (E)
  204709. STEREO
  204710. , AND DIASTEREOSELECTIVITY DEPENDING ON NUCLEOPHILES.
  204711. 15874N
  204712. 2/28/96
  204713. A_HIGHLY REGIOSELECTIVE PALLADIUM
  204714. MEDIATED SUBSTITUTION OF ALLYLIC AND DIENYLIC CYCLIC CARBONATES
  204715. 1994X    2357
  204716. 2360Y
  204717. 14866
  204718. DIDIER, E.
  204719. Tet. Lett.
  204720. $A NEW ROUTE FOR SEMISYNTHETIC DOCETAXEL, 1, IS DESCRIBED USING 2
  204721. MONOSUBSTITUTED
  204722. PHENYL
  204723. OXAZOLIDINE
  204724. CARBOXYLIC ACIDS IN ESTERIFICATION OF 7,10
  204725. DITROC
  204726. DESACETYLBACCATIN III (4). SUBSEQUENT DEPROTECTION OF ESTERS 10(+10') AFFORDED TITLE COMPOUND 1 WITHOUT REMOVAL OF THE BOC GROUP.
  204727. 15875N
  204728. 2/28/96
  204729. MONOSUBSTITUTED
  204730. OXAZOLIDINES AS IMPROVED PROTECTIVE GROUPS OF N
  204731. PHENYLISOSERINE IN DOCETAXEL PREPARATION
  204732. 1994X    2349
  204733. 2352Y
  204734. 14867
  204735. AUBERT, C.
  204736. Tet. Lett.C-ONE
  204737. STEP CONSTRUCTION CYCLIZATION 
  204738. FRAMEWORK 
  204739. FOR THE FIRST TIME, ALLENES WERE INVOLVED IN COBALT
  204740. MEDIATED  2+2+2 CYCLOADDITION REACTIONS, THE h4
  204741. COBALT COMPLEXES WERE ISOLATED. DECOMPLEXATION ON SILICA GEL LED TO THE CORRESPONDING FREE LIGANDS.
  204742. 15876N
  204743. 2/28/96
  204744. AYALLENES AS NEW PARTNERS IN INTRAMOLECULAR COBALT
  204745. MEDIATED [2+2+2] CYCLOADDITION REACTIONS
  204746. 1994X    2341
  204747. 2344Y
  204748. 14868
  204749. WEI, Z. Y.
  204750. Tet. Lett.
  204751. AMINO
  204752. ACID SYNTHESIS b
  204753. THE A
  204754. ESTER GROUP OF N
  204755. PROTECTED DIETHYL ASPARTATE (1A) OR DIETHYL GLUTAMATE (1B) WAS SELECTIVELY REDUCED USING DIISOBUTYLALUMINUM HYDRIDE (DIBALH) IN THE PRESENCE OF A LITHIUM TRIALKYLPHOSPHONOACETATE (2) TO AFFORD N
  204756. PROTECTED G
  204757. AMINO
  204758. UNSATURATED DICARBOXYLATES (4).
  204759. 15877N
  204760. 2/28/96
  204761. AyA REGIOSELECTIVE TANDEM REDUCTION 
  204762.  WITTIG
  204763. HORNER REACTION INVOLVING THE A
  204764. ESTER MOIETY OF DIETHYL ASPARTATE OR GLUTAMATE
  204765. 1994X    2305
  204766. 2308Y
  204767. 14869
  204768. CUNICO, R. F.
  204769. Tet. Lett.C
  204770. REARRANGEMENT 
  204771. ELECTROPHILICALLY INITIATED 1, 2
  204772. TMS GROUP MIGRATION
  204773. ELIMINATION WITHIN BIS(O
  204774. TMS) AND 1
  204775. TMS), 1
  204776. MESYL) DERIVATIVES OF 1
  204777. ALKYN
  204778. DIOLS AFFORDS A
  204779. TMS ALLENONES.
  204780. 15878N
  204781. 2/28/96
  204782. A&SYNTHESIS OF A
  204783. TRIMETHYLSILYLALLENONES
  204784. 1994X    2291
  204785. 2294Y
  204786. 14870
  204787. SMITH, B. A.
  204788. Tet. Lett.C!POTASSIUM HYDRIDE REARRANGEMENTS 
  204789. IRRADIATION OF ACETYLENIC ETHERS IN METHANOL GIVES HOMOLOGATED ESTERS VIA A FORMAL  1,3
  204790. OXYGEN
  204791. CARBON MIGRATION INVOLVING A KETENE INTERMEDIATE.
  204792. 15879N
  204793. 2/28/96
  204794. A`THE PHOTOCHEMISTRY OF ACETYLENIC ETHERS 
  204795.  A NOVEL CARBON
  204796. OXYGEN TO CARBON
  204797. CARBON BOND CONVERSION
  204798. 1994X    2283
  204799. 2286Y
  204800. 14871
  204801. CHOI, W. B.
  204802. Tet. Lett.CESTEREOCONTROLLED SYNTHESIS 
  204803. ANTIBIOTICS 
  204804. ACID DERIVATIVES PRECURSORS 
  204805. s(3S,4S)
  204806. BUTYLDIMETHYLSILYLOXY)ETHYL
  204807. CARBOXYETHYL
  204808. AZETIDINONE 7A WAS PREPARED FROM (3R,4R)
  204809. ACETOXY
  204810. BUTYLDIMETHYLSILYLOXY)ETHYL 
  204811. AZETIDINONE 3 VIA A SEQUENCE INVOLVING COUPLING WITH 2,2,5
  204812. TRIMETHYL
  204813. DIOXAN
  204814. DIONE 4, N
  204815. SILYLATION, SOLVOLYSIS OF THE METHYLMELDRUM'S ACID MOIETY AND A STEREOSELECTIVE ACID CATALYZED DECARBOXYLATION.
  204816. 15880N
  204817. 2/28/96
  204818. AoA STEREOSELECTIVE SYNTHESIS OF A KEY 1-b
  204819. METHYLCARBAPENEM INTERMEDIATE VIA A DIASTEREOSELECTIVE DECARBOXYLATION
  204820. 1994X    2275
  204821. 2278Y
  204822. 14872
  204823. MURAYAMA, T.
  204824. Tet. Lett.C
  204825. CARBAPENEM ANTIBIOTICS ACID 
  204826. ?A SIMPLE, HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF THE KEY 1-B
  204827. METHYLCARBAPENEM INTERMEDIATE 1 HAS BEEN ACCOMPLISHED VIA A PALLADIUM CATALYZED DEALLYLOXYCARBONYLATION OF DIALLYL MALONATE DERIVATIVE 4A WHICH WAS READILY PREPARED FROM (3S,4R)
  204828. ACETOXY
  204829. BUTYLDIMETHYLSILYLOXY) ETHYL
  204830. AZETIDIMONE 2 IN TWO STEPS.
  204831. 15881N
  204832. 2/28/96
  204833. A SIMPLE AND HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF A 1-b
  204834. METHYLCARBAPENEM KEY INTERMEDIATE BY DEALLYLOXYCARBONYLATION USING PALLADIUM COMPLEXES
  204835. 1994X    2271
  204836. 2274Y
  204837. 14873
  204838. ENGEL, P. S.
  204839. Tet. Lett.
  204840. LASER PHOTOCHEMISTRY TRIPLET DIRADICALS AZOALKANES 
  204841. BIRADICALS SUBSTITUTION 
  204842. KINETICS
  204843. THE LIFETIME (t) OF THE TRIPLET 1
  204844. CYCLOPROPYLCYCLOPENTANE
  204845. DIYL BIRADICAL (6) HAS BEEN DETERMINED BY THE CYCLOPROPYL CARBINYL RADICAL CLOCK METHOD TO BE 4 
  204846.  14 NS. THIS VALUE IS MUCH LONGER THAN THAT OF THE NONCYCLOPROPYL ANALOG 2 BUT IS SHORTER THAN T OF THE NORMETHYL ANALOG 5. THESE RESULTS SUPPORT THE EXISTENCE OF THE GEM
  204847. DIMETHYL EFFECT BUT BRING INTO QUESTION THE PREVIOUSLY REPORTED VERY SHORT T OF 2.
  204848. 15882N
  204849. 2/28/96
  204850. AkLIFETIME OF THE 2,2
  204851. DIMETHYLCYCLOPENTANE
  204852. DIYL BIRADICAL BY THE CYCLOPROPYLCARBINYL RADICAL CLOCK METHOD
  204853. 1994X    2267
  204854. 14874
  204855. BELLINA, F.
  204856. TetrahedronC
  204857. BIFUNCTIONAL REAGENTS CONVENIENT SYNTHESIS SELECTIVE SYNTHESIS 
  204858. ALKYL 2
  204859. ALKENOATES STANNYL
  204860. CUPRATION PALLADIUM 
  204861. VINYLSTANNANES ACETYLENES HYDROSTANNATION ALLYLAMINES 
  204862. TRIBUTYLSTANNYL
  204863. PROPEN
  204864. YL ACETATE (2), WHICH CAN BE EASILY PREPARED FROM ETHYL PROPYNOATE (5), REPRESENTS A USEFUL PRECURSOR TO A VARIETY OF 2
  204865. TRIBUTYLSTANNYL
  204866. ALKENES OF GENERAL FORMULA 1. THUS, TREATMENT OF 2 WITH COMPLEX ORGANOCOPPER SPECIES OF GENERAL FORMULA RCU
  204867. MGBRX
  204868. LIBR (4) (R = ALKYL, ARYL, BENZYL, ALLYL) AFFORDS COMPOUNDS 1 IN FAIR TO EXCELLENT YIELDS. HOWEVER, THIS PROCEDURE IS UNSUCCESSFUL FOR THE PREPARATION OF 2
  204869. TRIBUTYLSTANNYL
  204870. PENTADIENE (1E) AND 2,3
  204871. BIS(TRIBUTYL B&STANNYL)
  204872. PROPENE (1G). NEVERTHELESS,
  204873. 15883N
  204874. 2/28/96
  204875. AUSYNTHESIS OF 2
  204876. TRIBUTYLSTANNYL
  204877. ALKENES FROM 2
  204878. TRIBUTYLSTANNYL
  204879. PROPEN
  204880. YL ACETATE
  204881. 1994X    4853
  204882. 4872Y
  204883. 14875
  204884. FABER, W. S.
  204885. Tetrahedron
  204886. AlASYMMETRIC
  204887. SYNTHESIS CINCHONA ALKALOIDS AROMATIC THIOLS G
  204888. LACTONES 
  204889. COMBINED 
  204890. DERIVATIVES 
  204891. ENANTIOMERS 
  204892. THE KINETIC RESOLUTION OF RACEMIC 5
  204893. ALKOXY
  204894. 2(5H)
  204895. FURANONES, USING A CHIRAL AMINOALCOHOL CATALYZED 1
  204896. ADDITION OF ARYLTHIOLS, WAS EXAMINED. USING VARIOUS BUTENOLIDES IT WAS SHOWN THAT A G
  204897. ALKOXY SUBSTITUENT APPEARS TO BE ESSENTIAL TO REACH HIGH ENANTIOSELECTIVITIES WHEREAS ELECTRON
  204898. DONATING SUBSTITUENTS IN THE ARYLTHIOLS ALSO INCREASE THE SELECTIVITY. CINCHONA ALKALOIDS ARE THE PREFERRED CATALYSTS FOR THE KINETIC RESOLUTION, WITH QUININE AND QUINIDINE LEADING TO THE MOST EFFICIENT AND SELEB3CTIVE THIOL ADDITIONS. A REMARKABLE DILUTION EFFECT
  204899. 15884N
  204900. 2/28/96
  204901. A8CATALYTIC KINETIC RESOLUTION OF 5
  204902. ALKOXY
  204903. 2(5H)
  204904. FURANONES
  204905. 1994X    4775
  204906. 4794Y
  204907. 14876
  204908. GRISSOM, J. W.
  204909. Tetrahedron
  204910. POTENT ANTITUMOR ANTIBIOTICS
  204911. FORMYLALKYL RADICALS INTRAMOLECULAR ADDITION TRIGGERING DEVICES DESIGNED ENEDIYNES CHEMICAL SYNTHESIS MOLECULAR DESIGN 
  204912. GROUP MIGRATION DYNEMICIN
  204913. A CHEMISTRY 
  204914. PREVIOUS REPORTS HAVE SHOWN THAT THE THERMOLYSIS OF AROMATIC ENEDIYNES CONTAINING RADICAL ACCEPTING TETHERS WILL UNDERGO TANDEM ENEDIYNE
  204915. RADICAL CYCLIZATIONS. HEREIN WILL BE REPORTED SEVERAL EXAMPLES OF THE TANDEM ENEDIYNE
  204916. RADICAL CYCLIZATION WHERE NON
  204917. RADICAL ACCEPTING TETHERS WILL UNDERGO CYCLIZATIONS TO AROMATIC RINGS TO RESULT IN CYCLIZATION PRODUCTS. MOST OF THE UNUSUAL PRODUCTS RESULT FROM 1,5
  204918. HYDROGEN ABSTRACTION, FOLLOWED BY EITHER P
  204919. ELIMINATION OR RADICAL ADDITION TO THE AROMA
  204920. B>TIC RING. THE SYNTHESIS OF THE AROMATIC ENEDIYNES, MECHANISMS,
  204921. 15885N
  204922. 2/28/96
  204923. A]HIGH TEMPERATURE RADICAL CYCLIZATION ANOMALIES IN THE TANDEM ENEDIYNE
  204924. RADICAL CYCLIZATION
  204925. 1994X    4635
  204926. 4650Y
  204927. 14877
  204928. KODUKULLA, R. P. K.
  204929. Tetrahedron
  204930. CYCLOADDITION 3
  204931. NITRO
  204932. PHENYL
  204933. BENZOPYRANS BENZOPYRANOPYRAZOLE BENZOPYRANOPYRAZOLINE ANTIMICROBIAL 3,5
  204934. DIPHENYL
  204935. PYRAZolE 
  204936. DERIVATIVES 
  204937. ADDITIONS 
  204938. AGENTS 
  204939. A SERIES OF 3
  204940. NITRO
  204941. PHENYL
  204942. BENZOPYRANS (3A
  204943. H) WERE PREPARED AND TREATED WITH DIAZOMETHANE AND DIAZOETHANE TO GIVE VARIOUS BENZOPYRANOPYRAZOLE DERIVATIVES NAMELY  1,9
  204944. B(DIHYDRO
  204945. NITRO
  204946. PHENYL 1)BENZOPYRANO [3,4
  204947. C]PYRAZOLINES(4A
  204948. H), 4
  204949. PHENYL 1 BENZOPYRANO  [3,4
  204950. C]PYRAZOLES (5A
  204951. H) AND  1,9
  204952. B(DIHYDRO
  204953. MEtHYL
  204954. NITRO
  204955. PHENYl1)BENZOPYRANO [3,4
  204956. C]PYRAZOLINES(6A
  204957. H) RESPECTIVELY. THE REGIO AND STEREOCHEMICAL OUTCOME OF THESE CYCLOADDITIONS ARE DISCUSSED. THE BENZOPYRANOPYRAZOLE DERIVAB)TIVES 4A
  204958. H AND 6A
  204959. H WERE TESTED FOR THEIR
  204960. 15886N
  204961. 2/28/96
  204962. STEREOCHEMICAL INVESTIGATION IN THE 1,3 DIPOLAR CYCLOADDITIONS OF 3
  204963. NITRO
  204964. PHENYl
  204965. BENZOPYRANS TO DIAZOALKANES 
  204966.  SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF NOVEL BENZOPYRANOPYRAZOLE DERIVATIVES
  204967. 1994X    4623
  204968. 4634Y
  204969. 14878
  204970. KANE, V. V.
  204971. TetrahedronM
  204972. 15887N
  204973. 2/28/96
  204974. SYNTHESIS OF SMALL CYCLOPHANES
  204975. 1994X    4575
  204976. 4622Y
  204977. 14879
  204978. SCOBIE, M.
  204979. J.C.S. Perkin Trans. 1K
  204980. (VOL 1, PG 203, 1994)M
  204981. 15888N
  204982. 2/28/96
  204983. AyTUMOUR
  204984. TARGETTED BORANES .1. COUPLING OF CLOSO
  204985. CARBORANES TO SUBSTITUTED 2
  204986. NITROIMIDAZOLES VIA 1,3
  204987. DIPOLAR CYCLOADDITION 
  204988. 1994X
  204989. 14880
  204990. A    YAGEN, B.
  204991. J.C.S. Perkin Trans. 1C*ANTIMALARIAL DRUG QINGHAOSU 
  204992. ARTEMISININ 
  204993. 15889N
  204994. 2/28/96
  204995. AnTANDEM SILICA GEL
  204996. CATALYSED REARRANGEMENTS AND SUBSEQUENT BAEYER
  204997. VILLIGER REACTIONS OF ARTEMISININ DERIVATIVES
  204998. 1994X
  204999. 843-846Y
  205000. 14881
  205001. WATANABE, M.
  205002. J.C.S. Perkin Trans. 1CmASYMMETRIC
  205003. SYNTHESIS ARYL ALDEHYDES DIALKYLZINCS 
  205004. REAGENTS 
  205005. INDUCTION 
  205006. EPHEDRINE 
  205007. EFFICIENT 
  205008. ALCOHOLS 
  205009. SALTS M
  205010. 15890N
  205011. 2/28/96
  205012. ArENANTIOSELECTIVE ADDITION OF DIETHYLZINC TO ALDEHYDES USING CHIRAL POLYMER CATALYSTS POSSESSING A METHYLENE SPACER
  205013. 1994X
  205014. 837-842Y
  205015. 14882
  205016. TOKUDA, M.
  205017. J.C.S. Perkin Trans. 1
  205018. AEANODIC
  205019. OXIDATION D
  205020. ALKENYLAMINES
  205021. IMINYL RADICALS 
  205022. AMINIUM PRECURSORS 
  205023. 15891N
  205024. 2/28/96
  205025. NEW STEREOSELECTIVE SYNTHESIS OF TRANS
  205026. DISUBSTITUTED PYRROLIDINES BY CYCLIZATION OF AMINYL RADICALS GENERATED FROM 2
  205027.  AND/OR 5
  205028. SUBSTITUTED N
  205029. CHLORO
  205030. ALKYLALK
  205031. ENYLAMINES WITH BU3SNH
  205032. AZOISOBUTYRONITRILE
  205033. 1994X
  205034. 777-778Y
  205035. 14883
  205036. A    OJIMA, I.
  205037. JACSC
  205038. WARRENER RNM
  205039. 15892N
  205040. 2/28/96
  205041. AdA TANDEM CYCLOADDITION PROTOCOL FOR THE CONTROLLED SYNTHESIS OF [N]LADDERANES 
  205042.  NEW RODS AND SPACERS
  205043. 1994 APR 20;116(8):3645
  205044. 3646X    3645-3646Y
  205045. 14884
  205046. A    OJIMA, I.
  205047. JACSM
  205048. 15893N
  205049. 2/28/96
  205050. AOEXTREMELY CHEMOSELECTIVE SILYLFORMYLATION AND SILYLCARBOCYCLIZATION OF ALKYNALS
  205051. 1994 APR 20;116(8):3643
  205052. 3644X    3643-3644Y
  205053. 14885
  205054. ARDUENGO, A. J.
  205055. JACSM
  205056. 15894N
  205057. 2/28/96
  205058. A#A BIS(CARBENE) ADDUCT OF IODINE(1+)
  205059. 1994 APR 20;116(8):3625
  205060. 3626X    3625-3626Y
  205061. 14886
  205062. MENGER, F. M.
  205063. JACSM
  205064. 15895N
  205065. 2/28/96
  205066. AVA SELF
  205067. REPLICATING SYSTEM 
  205068.  NEW EXPERIMENTAL DATA AND A NEW MECHANISTIC INTERPRETATION
  205069. 1994 APR 20;116(8):3613
  205070. 3614X    3613-3614Y
  205071. 14887
  205072. COREY, E. J.
  205073. JACSM
  205074. 15896N
  205075. 2/28/96
  205076. DEMONSTRATION OF THE SYNTHETIC POWER OF OXAZABOROLIDINE CATALYZED ENANTIOSELECTIVE DIELS
  205077. ALDER REACTIONS BY VERY EFFICIENT ROUTES TO CASSIOL AND GIBBERELLIC ACID
  205078. 1994 APR 20;116(8):3611
  205079. 3612X    3611-3512Y
  205080. 14888
  205081. A    Ma, B. Y.B
  205082. JACSC
  205083. GAUSSIAN BASIS FUNCTIONS ATOMIC BASIS SETS FIRST
  205084. ROW ATOMS 
  205085. MOLECULAR CALCULATIONS CONTRACTION 
  205086. VINYLIDENE 
  205087. DYNAMICS 
  205088. ETHYLENE 
  205089. ENERGIES M
  205090. 15897N
  205091. 2/28/96
  205092. A@SINGLET METHYLCARBENE 
  205093.  EQUILIBRIUM GEOMETRY OR TRANSITION STATE
  205094. 1994 APR 20;116(8):3539
  205095. 3542X    3539-3542Y
  205096. 14889
  205097. Lim, D. C.B
  205098. AFPOTENTIAL FUNCTIONS SIMULATIONS 
  205099. DERIVATIVES 
  205100. ENERGIES 
  205101. ETHERS 
  205102. MCSCF 
  205103. 15898N
  205104. 2/28/96
  205105. ApSOLVENT EFFECTS ON THE RING OPENING OF CYCLOPROPANONES TO OXYALLYLS 
  205106.  A COMBINED AB INITIO AND MONTE CARLO STUDY
  205107. 1994 APR 20;116(8):3494
  205108. 3499X    3494-3499Y
  205109. 14890
  205110. Bach, R. D.B
  205111. PLESSET PERTURBATION
  205112. THEORY MICROSOMAL CYTOCHROME
  205113. 450 HYDROCARBON PROPERTIES THEORETICAL
  205114. ANALYSIS 
  205115. ATOM TRANSFER 
  205116. WATER 
  205117. OXIDE 
  205118. CALIBRATION CLOCKS 
  205119. ENERGY 
  205120. 15899N
  205121. 2/28/96
  205122. AUA MODEL FOR THE FREE RADICAL AND ELECTROPHILIC HYDROXYLATION OF BICYCLO[2.1.0]PENTANE
  205123. 1994 APR 20;116(8):3475
  205124. 3482X    3475-3482Y
  205125. 14891
  205126. PAQUETTE, L. A.
  205127. JACSC
  205128. CLAISEN REARRANGEMENT STEREOSPECIFIC SYNTHESIS VINYL ETHERS DEOXYGENATION ANNELATION 
  205129. ANNULATION 
  205130. ALDEHYDES 
  205131. KETONES 
  205132. ESTERS 
  205133. ACID M
  205134. 15900N
  205135. 2/28/96
  205136. TOTAL SYNTHESIS OF THE CEMBRANOID DITERPENE LACTONE (+)
  205137. CLEOMEOLIDE 
  205138.  SOME REMARKABLE CONFORMATIONAL FEATURES OF NINE
  205139. MEMBERED BELTS LINKED IN 2,6
  205140. FASHION TO A METHYLENE CYCLOHEXANE CORE
  205141. 1994 APR 20;116(8):3367
  205142. 3374X    3367-3374Y
  205143. 14892
  205144. HUDSON, C. M.
  205145. TEMPORARY SILICON CONNECTION 
  205146. DIELS
  205147. ALDER REACTIONS CARBON NMR
  205148. SPECTRA ELECTROCHEMICAL OXIDATION RADICAL CYCLIZATION STEREOCONTROLLED SYNTHESIS 
  205149. ORGANOSILICON COMPOUNDS 
  205150. ALLYLIC ALCOHOLS 
  205151. TOTAL ASSIGNMENT STEREOSELECTIVITY 
  205152. 15901N
  205153. 2/28/96
  205154. AKINTRAMOLECULAR ANODIC OLEFIN COUPLING REACTIONS AND THE USE OF VINYLSILANES
  205155. 1994 APR 20;116(8):3347
  205156. 3356X    3347-3356Y
  205157. 14893
  205158. ORGAN, M. G.
  205159. MODELING CHEMICAL
  205160. REACTIVITY MOLECULAR
  205161. ORBITAL METHODS DIASTEREOFACIAL SELECTIVITY TRANSITION STRUCTURES CONJUGATE ADDITIONS d
  205162. LACTONES 
  205163. ALLYLIC BONDS 1,3
  205164. DIOXIN
  205165. ONES STEREOSELECTIVITY CYCLOCONDENSATION 
  205166. 15902N
  205167. 2/28/96
  205168. PHOTOADDITIONS AND DIALKYLCUPRATE ADDITIONS TO 2
  205169. BUTYL
  205170. DIMETHYL
  205171. DIOXIN
  205172. ONE AND RELATED HETEROCYCLES 
  205173.  EXPERIMENTAL, AB INITIO THEORETICAL, AND X
  205174. RAY STRUCTURAL STUDIES OF FACIAL SELECTIVITY AND ENONE PYRAMIDALIZATION
  205175. 1994 APR 20;116(8):3312
  205176. 3323X    3312-3323Y
  205177. 14894
  205178. Wang, P.B
  205179. AFH INSERTION 
  205180. RHODIUM(II) CARBOXYLATE CATALYZED
  205181. REACTIONS CONSTRUCTION 
  205182. 15903N
  205183. 2/28/96
  205184. AaMODEL STUDIES OF THE STEREOELECTRONIC EFFECT IN RH(II) MEDIATED CARBENOID C
  205185. H INSERTION REACTIONS
  205186. 1994 APR 20;116(8):3296
  205187. 3305X    3296-3305Y
  205188. 14895
  205189. Beak, P.B
  205190. JACSC
  205191. ORGANOMETALLIC REAGENTS CHIRALITY TRANSFER GRIGNARD
  205192. REAGENTS ALKYLATION 
  205193. SPARTEINE DERIVATIVES LITHIATION 
  205194. INDUCTION CHEMISTRY NITROGEN M
  205195. 15904N
  205196. 2/28/96
  205197. AwCOMPLEX INDUCED PROXIMITY EFFECTS 
  205198.  ENANTIOSELECTIVE SYNTHESES BASED ON ASYMMETRIC DEPROTONATIONS OF N
  205199. PYRROLIDINES
  205200. 1994 APR 20;116(8):3231
  205201. 3239X    3231-3239Y
  205202. 14896
  205203. BRADSHAW, J. D.
  205204. JACSCWSTILBENE
  205205. LIKE COMPOUNDS PHOTODEHYDROCYCLIZATIONS HELICENES 
  205206. POLYMERS 
  205207. SYSTEMS 
  205208. CRYSTAL M
  205209. 15905N
  205210. 2/28/96
  205211. AfLITHIUM
  205212. INDUCED CYCLIZATION OF TETRABENZOCYCLYNE 
  205213.  A NOVEL ZIPPER REACTION OF CYCLIC O
  205214. ETHYNYLBENZENES
  205215. 1994 APR 20;116(8):3177
  205216. 3179X    3177-3179Y
  205217. 14897
  205218. IsHII,  A.
  205219. Angew. Chem. Int. Ed. Engl. M
  205220. 15906N
  205221. 2/28/96
  205222. A:THE FIRST ISOLABLE DITHIIRANE BY OXIDATION OF A DITHIETANE
  205223. 1994 APR 18;33(7):777
  205224. 777-779Y
  205225. 14898
  205226. TROMMER, M.
  205227. Angew. Chem. Int. Ed. Engl. M
  205228. 15907N
  205229. 2/28/96
  205230. DIMETHYL
  205231. SILIRENE
  205232. 1994 APR 18;33(7):766
  205233. 766-769Y
  205234. 14899
  205235. HOLTHAUSEN,  M. C.
  205236. Angew. Chem. Int. Ed. Engl. M
  205237. 15908N
  205238. 2/28/96
  205239. Au1(9)
  205240. HOMOCUBENE AND 9
  205241. HOMOCUBYLIDENE 
  205242.  THEORETICAL INVESTIGATION OF STRUCTURES, ENERGIES, AND REARRANGEMENT REACTIONS
  205243. 1994 MAR 31;33(6):668
  205244. 668-670Y
  205245. 14900
  205246. A    IBUKA, T.
  205247. Angew. Chem. Int. Ed. Engl. M
  205248. 15909N
  205249. 2/28/96
  205250. A NOVEL ROUTE TO DIASTEREOMERICALLY PURE (E)
  205251. ALKENE DIPEPTIDE ISOSTERES FROM b
  205252. AZIRIDINYL
  205253. ENOATES BY TREATMENT WITH ORGANOCOPPER REAGENTS
  205254. 1994 MAR 31;33(6):652
  205255. 652-654Y
  205256. 14901
  205257. TANNER, D.
  205258. Angew. Chem. Int. Ed. Engl. M
  205259. 15910N
  205260. 2/28/96
  205261. ANCHIRAL AZIRIDINES 
  205262.  THEIR SYNTHESIS AND USE IN STEREOSELECTIVE TRANSFORMATIONS
  205263. 1994 MAR 31;33(6):599
  205264. 599-619Y
  205265. 14902
  205266. HODGSON, D. M.
  205267. Tet. Lett.C
  205268. ORGANOCHROMIUM 
  205269. AzTHE SYNTHESIS OF FUNCTIONALISED E
  205270. ALKENYLSTANNANES FROM ALDEHYDES AND A MIXTURE OF BU3SNCHBR2, LII AND CRCL2 IS DESCRIBED.
  205271. 15911N
  205272. 2/28/96
  205273. AkCHEMOSELECTIVITY IN THE CHROMIUM(II)
  205274. MEDIATED SYNTHESIS OF E
  205275. ALKENYLSTANNANES FROM ALDEHYDES AND BU3SNCHBR2
  205276. 1994 APR 4;35(14):2231
  205277. 2234X    2231-2234Y
  205278. 14903
  205279. HORWELL, D. C.
  205280. Tet. Lett.
  205281. THE FORMATION OF A SUBSTITUTED BICYCLE [3.2.0] HEPT
  205282. ONE (2), AND ITS SUBSEQUENT REDUCTION AND CYCLISATION TO (6), VIA AN INTRAMOLECULAR BROMOETHERIFICATION, IS DESCRIBED.
  205283. 15912N
  205284. 2/28/96
  205285. AfFORMATION OF THE OXATRICYCLO[3.2.1.0(3,6)]OCTANE RING SYSTEM VIA AN INTRAMOLECULAR BROMOETHERIFICATION
  205286. 1994 APR 4;35(14):2221
  205287. 2222X    2221-2222Y
  205288. 14904
  205289. APPENDINO, G.
  205290. Tet. Lett.C
  205291. CHEMISTRY 
  205292. TAXANES 
  205293. TREATMENT OF 7
  205294. TRIETHYLSILYL
  205295. HYDROXY
  205296. DEACETYLBACCATIN III (1B) WITH PYRIDINIUM P
  205297. TOLUENESULFONATE IN REFLUXING BENZENE GAVE THE ORTHOESTER 3 AS A RESULT OF O(2) 
  205298. > O(14) BENZOATE MIGRATION, CONTRACTION OF RING A FOLLOWED BY FORMATION OF AN ETHER BRIDGE BETWEEN C(15) AND C(10), AND REARRANGEMENT OF THE 4
  205299. ACETOXY
  205300. 5(20)
  205301. OXETANE MOIETY INTO A C(5)
  205302. EPIMERIZED 2,4,20
  205303. ORTHOACETATE.
  205304. 15913N
  205305. 2/28/96
  205306. A+A NEW REARRANGEMENT OF OXETANE
  205307. TYPE TAXOIDS
  205308. 1994 APR 4;35(14):2217
  205309. 2220X    2217-2220Y
  205310. 14905
  205311. A    Ho, T. L.B
  205312. Tet. Lett.
  205313. TREATMENT OF 6
  205314. NITROBICYCLO[2.2.1]HEPT
  205315. ENES WITH TIN(II) CHLORIDE IN REFLUXING THF OR DIOXANE GAVE 3
  205316. ARYLPYRIDINES VIA A DEEP
  205317. SEATED REARRANGEMENT.
  205318. 15914N
  205319. 2/28/96
  205320. AZREDUCTIVE REARRANGEMENT OF 5
  205321. NITROBICYCLO[2.2.1]HEPT
  205322. ENES 
  205323.  FORMATION OF 3
  205324. ARYLPYRIDINES
  205325. 1994 APR 4;35(14):2211
  205326. 2212X    2211-2212Y
  205327. 14906
  205328. A    Naito, T.B
  205329. Tet. Lett.
  205330. CTRADICAL CYCLIZATION 
  205331. OXIME 
  205332. ETHER 
  205333. AMINO ALCOHOL 
  205334. TRIBUTYLTIN HYDRIDE 
  205335. OXIME ETHERS 
  205336. OXIME ETHERS CONNECTED BY A TETHER TO ALDEHYDES OR KETONES EFFICIENTLY CYCLIZE IN A FREE RADICAL CYCLIZATION WHICH IS MEDIATED BY TRIBUTYLTIN HYDRIDE AND PROVIDE A NEW ENTRY TO THE CYCLIC AMINO ALCOHOLS.
  205337. 15915N
  205338. 2/28/96
  205339. AoRADICAL CYCLIZATIONS OF OXIME ETHERS CONNECTED WITH ALDEHYDES OR KETONES 
  205340.  A NEW ENTRY TO CYCLIC AMINO ALCOHOLS
  205341. 1994 APR 4;35(14):2205
  205342. 2206X    2205-2206Y
  205343. 14907
  205344. Lee, G. H.B
  205345. Tet. Lett.C
  205346. REAGENT 
  205347. SYSTEM 
  205348. MILD 
  205349. AN EXTREMELY CONVENIENT DEOXYGENATION OF 1
  205350. ALKENYL, ALKYL, AND ARYL PHENYL SULFOXIDES WITH MAGNESIUM POWDER IN ABSOLUTE METHANOL (OR ETHANOL) AFFORDED THE CORRESPONDING SULFIDES IN EXCELLENT YIELDS.
  205351. 15916N
  205352. 2/28/96
  205353. AN EFFICIENT DEOXYGENATION OF 1
  205354. ALKENYL OR ALKYL PHENYL SULFOXIDES TO THE CORRESPONDING SULFIDES MEDIATED BY MAGNESIUM IN ALCOHOL
  205355. 1994 APR 4;35(14):2195
  205356. 2196X    2195-2196Y
  205357. 14908
  205358. SAKURAI, O.
  205359. Tet. Lett.C#THIENAMYCIN ANTIBIOTICS DERIVATIVES
  205360. METHYLCARBAPENEMS 7 WERE SYNTHESIZED UTILIZING THE ESCHENMOSER SULFIDE CONTRACTION AS A KEY STEP IN A ONE
  205361. POT PROCEDURE FROM THE NOVEL THIAZINONE INTERMEDIATE 4 WHICH WAS EASILY ACCESSIBLE FROM THE PROPIONIC ACID DERIVATIVE 1.
  205362. 15917N
  205363. 2/28/96
  205364. A]A NEW SYNTHETIC METHOD Of 1 b
  205365. METHYLCARBAPENEMS UTILIZING THE ESCHENMOSER SULFIDE CONTRACTION
  205366. 1994 APR 4;35(14):2187
  205367. 2190X    2187-2190Y
  205368. 14909
  205369. A    MUKAI, C.
  205370. Tet. Lett.C%EPOXIDE OPENINGS SYSTEMS 
  205371. ACTIVATION 
  205372. TREATMENT OF THE ACETYLENIC EPOXIDES 1 HAVING ELECTRON
  205373. DONATING GROUPS AT THE ACETYLENIC TERMINUS WITH A CATALYTIC AMOUNT OF BF3.OET2 AFFORDED 6
  205374. ENDO PRODUCTS WITH INVERSION OF STEREOCHEMISTRY AT THE PROPYNYL POSITION IN A HIGHLY STEREOSELECTIVE MANNER, WHEREAS THE ACETYLENIC EPOXIDES 1 POSSESSING ELECTRON
  205375. WITHDRAWING SUBSTITUTENTS AT THE ACETYLENIC TERMINUS PROVIDED UNDER SIMILAR ACIDIC CONDITION THE CORRESPONDING TETRAHYDROFURAN DERIVATIVES IN A HIGHLY SELECTIVE WAY.
  205376. 15918N
  205377. 2/28/96
  205378. AqAN ALTERNATIVE PROCEDURE FOR THE STEREOSELECTIVE FORMATION OF TETRAHYDROPYRAN DERIVATIVES VIA 6
  205379. ENDO RING CLOSURE
  205380. 1994 APR 4;35(14):2183
  205381. 2186X    2183-2186Y
  205382. 14910
  205383. A    MUKAI, C.
  205384. Tet. Lett.C
  205385. POLYETHER ANTIBIOTICS STEREOCONTROLLED SYNTHESIS TETRAHYDROPYRAN SYSTEMS PROPARGYL CATIONS NATURAL
  205386. PRODUCTS 
  205387. EPOXIDE OPENINGS CONSTRUCTION 
  205388. CYCLIZATION 
  205389. ACTIVATION 
  205390. MONENSIN 
  205391. EFFICIENT ACCESS TO TETRAHYDROPYRAN DERIVATIVES VIA HIGHLY REGIO
  205392.  AND STEREOSELECTIVE 6
  205393. ENDO TET MODE RING OPENING OF AN EPOXIDE BY AN INTERNAL HYDROXY GROUP HAS BEEN DEVELOPED.  COBALT COMPLEXES, DERIVED FROM TRANS
  205394. EPOXY
  205395. HEPTYN
  205396. OLS AND DICOBALT OCTACARBONYL WERE TREATED WITH A CATALYTIC AMOUNT OF BF3.OET2 IN CH2CL2 AT 
  205397.  C TO AFFORD CIS
  205398. ETHYNYL
  205399. HYDROXY TETRAHYDROPYRAN DERIVATIVES IN A HIGHLY REGIO
  205400.  AND STEREOSELECTIVE MANNER. SIMILAR TREATMENT OF CIS
  205401. EPOXIDES PROVIDED THE B1CORRESPONDING TRANS
  205402. TETRAHYDROPYRANS SELECTIVELY.
  205403. 15919N
  205404. 2/28/96
  205405. AuREGIOSELECTIVE AND STEREOSPECIFIC FORMATION OF 2
  205406. ETHYNYL
  205407. HYDROXYTETRAHYDROPYRAN DERIVATIVES VIA 6
  205408. ENDO RING CLOSURE
  205409. 1994 APR 4;35(14):2179
  205410. 2182X    2179-2182Y
  205411. 14911
  205412. FUKUYAMA, T.
  205413. Tet. Lett.
  205414. BOTH 1,1,1,3,3,3
  205415. HEXAMETHYLDISILAZANE AND N,O
  205416. (TRIMETHYLSILYL) ACETAMIDE HAVE BEEN SHOWN TO SUPPRESS THE FORMATION OF ABNORMAL AROMATIC CLAISEN REARRANGEMENT PRODUCTS BY EFFICIENTLY TRAPPING THE INCIPIENT NORMAL PRODUCTS aS THEIR SILYL ETHERS UNDER MILD CONDITIONS.
  205417. 15920N
  205418. 2/28/96
  205419. USE OF 1,1,1,3,3,3
  205420. HEXAMETHYLDISILAZANE AND N,O
  205421. (TRIMETHYLSILYL)ACETAMIDE IN AROMATIC CLAISEN REARRANGEMENT 
  205422.  AN EFFICIENT METHOD FOR PREVENTING ABNORMAL CLAISEN REARRANGEMENT
  205423. 1994 APR 4;35(14):2145
  205424. 2148X    2145-2148Y
  205425. 14912
  205426. A    ROZEN, S.
  205427. Tet. Lett.C
  205428. SULFOXIDES 
  205429. OXIDATION 
  205430. THE HOF.CH3CN COMPLEX, MADE DIRECTLY BY PASSING FLUORINE THROUGH AQUEOUS ACETONITRILE, OXIDIZES ALL TYPES OF SULFIDES TO THE CORRESPONDING SULFONES AND ALSO OFFERING A WAY TO MAKE O
  205431. 18 CONTAINING SULFONE DERIVATIVES.
  205432. 15921N
  205433. 2/28/96
  205434. AYA NOVEL AND EFFICIENT METHOD FOR OXIDIZING SULFIDES TO SULFONES WITH THE HOF
  205435. CH3CN SYSTEM
  205436. 1994 MAR 28;35(13):2099
  205437. 2100X    2099-2100Y
  205438. 14913
  205439. COLOMBO, L.
  205440. Tet. Lett.
  205441. AcASYMMETRIC
  205442. SYNTHESIS ACYL ANION 
  205443. ALDEHYDES 
  205444. GENERATION 
  205445. ALCOHOLS 
  205446. REAGENTS 
  205447. GLYCOLS 
  205448. OXIDES 
  205449. ACIDS 
  205450. THE PREPARATION OF ENANTIOMERICALLY PURE 2
  205451. LITHIO
  205452. DIOXOLANES AND 2
  205453. LITHIOOXAZOLIDINES AND THEIR USE AS FORMYL ANION EQUIVALENTS IN ADDITION REACTIONS TO ALDEHYDES ARE DESCRIBED.
  205454. 15922N
  205455. 2/28/96
  205456. AVCHIRAL 2
  205457. LITHIO
  205458. DIOXOLANES AND 2
  205459. LITHIOOXAZOLIDINES 
  205460.  NEW FORMYL ANION EQUIVALENTS
  205461. 1994 MAR 28;35(13):2063
  205462. 2066X    2063-2066Y
  205463. 14914
  205464. PEDREGAL, C.
  205465. Tet. Lett.
  205466. A"AMINO
  205467. ACIDS 
  205468. DERIVATIVES 
  205469. PROLINE 
  205470. BOC PROTECTED LACTAMS CAN BE REDUCED CHEMOSELECTIVELY IN THE PRESENCE OF OTHER GROUPS SUCH AS ESTERS, NITRILES, CARBAMATES OR DOUBLE BONDS BY FIRST REDUCING THE AMIDE CARBONYL GROUP INTO THE CORRESPONDING HEMIAMINAL USING LITHIUM TRIETHYLBOROHYDRIDE FOLLOWED BY FURTHER REDUCTION OF THE HEMIAMINAL INTERMEDIATE WITH TRIETHYLSILANE/BORON TRIFLUORIDE ETHERATE. THIS METHOD PRESERVES THE CHIRALITY PRESENT IN THE SUBSTRATE.
  205471. 15923N
  205472. 2/28/96
  205473. A:HIGHLY CHEMOSELECTIVE REDUCTION OF N
  205474. BOC PROTECTED LACTAMS
  205475. 1994 MAR 28;35(13):2053
  205476. 2056X    2053-2056Y
  205477. 14915
  205478. DORTA, R. L.
  205479. Tet. Lett.
  205480. RIBONOLACTONE ORGANIC
  205481. SYNTHESIS 
  205482. CARBOHYDRATES POSSESSING A SUITABLY POSITIONED HYDOXYL GROUP IN THE PRESENCE OF ORGANOSELENIUM REAGENTS AND IODINE UNDER AN ARGON ATMOSPHERE UNDERGO INTRAMOLECULAR B
  205483. FRAGMENTATION CYCLIZATION REACTION TO GIVE ALDOFURANOSE AND ALDOPYRANOSE FORMS OF CARBOHYDRATES, SPECIFICALLY.
  205484. 15924N
  205485. 2/28/96
  205486. AjORGANOSELENIUM REAGENTS IN THE TANDEM b
  205487. FRAGMENTATION CYCLIZATION OF CARBOHYDRATE ANOMERIC ALKOXY RADICALS
  205488. 1994 MAR 28;35(13):2049
  205489. 2052X    2049-2052Y
  205490. 14916
  205491. EASTWOOD, F. W.
  205492. Tet. Lett.C MARINE METABOLITES HALICHONDRIA 
  205493. RING ENLARGEMENT OF N
  205494. ACYLAZIRIDINES FOLLOWED BY NICKEL PEROXIDE OXIDATION PROVIDES A VARIETY OF 2,4
  205495. DISUBSTITUTED
  205496. OXAZOLES SUITABLE FOR BIS
  205497.  AND TRIS
  205498. OXAZOLE SYNTHESIS.
  205499. 15925N
  205500. 2/28/96
  205501. A-PREPARATION OF NEW 2,4
  205502. DISUBSTITUTED OXAZOLES
  205503. 1994 MAR 28;35(13):2039
  205504. 2042X    2039-2042Y
  205505. 14917
  205506. ORIYAMA, T.
  205507. Tet. Lett.C
  205508. CHLORIDE 
  205509. ETHERS 
  205510. A REAGENT SYSTEM OF ACETYL BROMIDE COMBINED WITH A CATALYTIC AMOUNT OF TIN(II) BROMIDE CLEAVES READILY TRIALKYLSILYL ETHERS TO GIVE THE CORRESPONDING ACETATES IN HIGH YIELDS UNDER VERY MILD CONDITIONS.
  205511. 15926N
  205512. 2/28/96
  205513. AdA ONE
  205514. STEP AND CHEMOSELECTIVE CONVERSION OF SILYL
  205515. PROTECTED ALCOHOLS INTO THE CORRESPONDING ACETATES
  205516. 1994 MAR 28;35(13):2027
  205517. 2030X    2027-2030Y
  205518. 14918
  205519. HARNETT, J. J.
  205520. Tet. Lett.C
  205521. EPOXIDES 
  205522. OXETANES 
  205523. THE REACTION OF EXCESS DIMETHYLSULPHONIUM METHYLIDE WITH VARIOUS ALIPHATIC AND AROMATIC KETONES LEADS EXCLUSIVELY TO HOMOLOGATED ALLYLIC ALCOHOLS IN GOOD YIELDS.
  205524. 15927N
  205525. 2/28/96
  205526. ATA NOVEL SYNTHESIS OF HOMOLOGATED ALLYLIC ALCOHOLS USING DIMETHYLSULPHONIUM METHYLIDE
  205527. 1994 MAR 28;35(13):2009
  205528. 2012X    2009-2012Y
  205529. 14919
  205530. DUCHENET, V.
  205531. Tet. Lett.C
  205532. ADDUCTS 
  205533. @WHEN 12
  205534. CYANO
  205535.  (AND 11
  205536. SELENA)
  205537. DIHYDRO
  205538.  ETHANOANTHRACENES WERE DEPROTONATED AT 0
  205539.  C, THE RESULTING CARBANIONS UNDERWENT A WITTIG REARRANGEMENT. AFTER HYDROLYSIS OR ALKYLATION, 9,10
  205540. DIHYDRO
  205541. METHANOANTHRACENE DERIVATIVES WERE ISOLATED. THE FIRST SYNTHESIS OF A SELENO
  205542. CYANOHYDRINE IS ALSO DESCRIBED.
  205543. 15928N
  205544. 2/28/96
  205545. A_SYNTHESIS OF THIO
  205546. SUBSTITUTED AND SELENO
  205547. SUBSTITUTED METHANOANTHRACENES BY WITTIG REARRANGEMENT
  205548. 1994 MAR 28;35(13):2005
  205549. 2008X    2005-2008Y
  205550. 14920
  205551. DESARBRE, E.
  205552. Tet. Lett.C$AMINOPYRIDINES DERIVATIVES 
  205553. INDOLES 
  205554. SUBSTITUTED
  205555. PYRROLO[2,3
  205556. B]PYRIDIN
  205557. ONES (7
  205558. AZAINDOLINONES) HAVE BEEN OBTAINED BY BAEYER
  205559. VILLIGER OXIDATION.  REACTION OF 7
  205560. AZAINDOLINONE WITH AROMATIC ALDEHYDES LED TO 2
  205561. SUBSTITUTED 7
  205562. AZAINDOLINONES. SYNTHESIS OF PYRIDO[3',2':4,5]PYRROLO[3,2
  205563. B] NAPHTYRIDINE HAVE BEEN DESCRIBED.
  205564. 15929N
  205565. 2/28/96
  205566. AISYNTHESIS AND REACTIVITY OF 1
  205567. SUBSTITUTED
  205568. PYRROLO[2,3
  205569. PYRIDIN
  205570. 1994 MAR 28;35(13):1995
  205571. 1998X    1995-1998Y
  205572. 14921
  205573. BOURHIS, M.
  205574. Tet. Lett.
  205575. Az4+2 CYCLOADDITIONS ADDITION
  205576. REACTIONS 
  205577. NMR TRANS
  205578. (DIMETHYLAMINO)
  205579. BUTADIENE DIENENITRILES SPECTROSCOPY 
  205580. DIENES 
  205581. BOND 
  205582. HTHE REACTION OF ETHYL 2
  205583. DIMETHYLAMINO)PENTA
  205584. DIENOATE 4 WITH ACRYLONITRILE 2
  205585. GAVE THE METHYL N
  205586. METHYL
  205587. PROPENYL)
  205588. CYANO
  205589.  PYRROLIDINE
  205590. CARBOXYLATE 5A AND 5B AS A [3 + 2]
  205591. ATOMS CYCLOADDUCTS.  THE PUTATIVE [1,3] DIPOLAR INTERMEDIATE SPECIES AZOMETHINE YLIDE 4C, RESULTS FROM [1,6] HYDROGEN SHIFT OF ONE N(CH3) PROTON.
  205592. 15930N
  205593. 2/28/96
  205594. AaUNEXPECTED [3+2] CYCLOADDITION BETWEEN ETHYL A
  205595. DIMETHYLAMINO)PENTADIENOATE AND ACRYLONITRILE
  205596. 1994 MAR 28;35(13):1981
  205597. 1984X    1981-1984Y
  205598. 14922
  205599. REETZ, M. T.
  205600. Tet. Lett.
  205601. ERYTHRO
  205602. SPHINGOSINE D
  205603. THREO
  205604. SPHINGOSINE ORGANIC
  205605. SYNTHESIS L
  205606. SERINE 
  205607. ACIDS 
  205608. DERIVATIVES 
  205609. ISOSTERES 
  205610. LIGAND 
  205611.  AND CBZ
  205612. PROTECTED A
  205613. AMINO ALDEHYDES DERIVED FROM AMINO ACIDS UNDERGO STEREOSELECTIVE ADDITION REACTIONS WITH ALKYL CUPRATES AND MANGANESE REAGENTS, THE CHELATION
  205614. CONTROLLED ADDUCTS BEING THE MAJOR DIASTEREOMERS (GENERALLY DS ] 90%). UNDESIRED RACEMIZATION IS NOT OBSERVED (EE ] 99%).
  205615. 15931N
  205616. 2/28/96
  205617. AGA SIMPLE METHOD FOR CHELATION CONTROLLED ADDITIONS TO A
  205618. AMINO ALDEHYDES
  205619. 1994 MAR 28;35(13):1969
  205620. 1972X    1969-1972Y
  205621. 14923
  205622. MONIATTE,  M.
  205623. Tet. Lett.
  205624. AuOPEN
  205625. CHAIN (E)
  205626. DIENEDIYNE NEOCARZINOSTATIN CHROMOPHORE (Z)
  205627. DIENEDIYNE SYSTEMS DIENEDIYNES 
  205628. ALKYNES 
  205629. COUPLINGS 
  205630. ROUTE 
  205631. THE Z
  205632. CONFIGURATED BIS(ENOLTRIFLATES) 2 AND 7 WERE TREATED AT ROOM TEMPERATURE WITH TMS ACETYLENE (1.25 EQUIV.) IN THE PRESENCE OF CUI (0. 17 EQUIV.) AND VARIOUS PALLADIUM CATALYSTS (0.07 EQUIV.), SOLVENTS, AND AMINES TO AFFORD MONOCOUPLING PRODUCTS. SURPRISINGLY, OPPOSITE REGIOSELECTIVITIES WERE OBSERVED STARTING FROM THE FIVE
  205633. MEMBERED (
  205634. >8, N = 0) VS. THE SIX
  205635. MEMBERED BIS(ENOLTRIFLATES) (
  205636. >9, N = 1).
  205637. 15932N
  205638. 2/28/96
  205639. STUDY OF THE REGIOSELECTIVITY OF PALLADIUM
  205640. CATALYZED MONOCOUPLINGS BETWEEN CONJUGATED BIS(ENOLTRIFLATES) AND TRIMETHYLSILYLACETYLENE
  205641. 1994 MAR 28;35(13):1965
  205642. 1968X    1965-1968Y
  205643. 14924
  205644. MARKO, I. E.
  205645. Tetrahedron
  205646. A^MICROBIAL OXIDATION ORGANIC
  205647. SYNTHESIS STEREOCONTROLLED SYNTHESIS 
  205648. ADDITIONS 
  205649. REAGENTS
  205650. BENZENE 
  205651. 7CYCLOADDITION REACTIONS BETWEEN THE CHIRAL 2
  205652. PYRONE DERIVATIVES 9 AND VARIOUS DIENOPHILES, CATALYSED BY LANTHANIDE SHIFT REAGENTS, AFFORDED DIASTEREOMERICALLY PURE BICYCLIC LACTONES 3. A CATALYTIC ASYMMETRIC VERSION OF THESE REACTIONS, USING OPTICALLY ACTIVE LANTHANIDE CATALYSTS, WAS SUCCESSFULLY INVESTIGATED.
  205653. 15933N
  205654. 2/28/96
  205655. ABCATALYTIC ASYMMETRIC DIELS
  205656. ALDER REACTIONS OF 2
  205657. PYRONE DERIVATIVES
  205658. 1994 APR 11;50(15):4557
  205659. 4574X    4557-4574Y
  205660. 14925
  205661. A    Riant, O.B
  205662. Tetrahedron
  205663. DIELS
  205664. ALDER REACTIONS CHIRAL LEWIS
  205665. ACIDS ORGANIC
  205666. SYNTHESIS AMINO
  205667. ACIDS 
  205668. INDUCTION 
  205669. COMPLEXES 
  205670. ALDEHYDES 
  205671. ALKALOIDS 
  205672. POWERFUL ADDUCTS 
  205673. ANTHRONE HAS BEEN FOUND TO REACT WITH N
  205674. METHYLMALEIMIDE IN THE PRESENCE OF CATALYTIC AMOUNTS OF VARIOUS CHIRAL B
  205675. AMINO ALCOHOLS. THE CYCLOADDUCT 3A HAS BEEN OBTAINED IN EXCELLENT YIELD WITH ENANTIOMERIC EXCESS OF UP TO 61%. ITS ABSOLUTE CONFIGURATION HAS BEEN ASSIGNED BY X
  205676. RAY CRYSTALLOGRAPHY. SEVERAL FEATURES OF THE REACTION HAVE BEEN STUDIED: VARIATION OF DIENOPHILE; COMPETITION BETWEEN CYCLOADDITION AND FORMATION OF THE OPTICALLY ACTIVE MICHAEL ADDUCT 4; SOLVENT AND TEMPERATURE EFFECTS.B6 MECHANISTIC STUDIES ARE IN AGREEMENT WITH A CONCERTED
  205677. 15934
  205678. 2/28/96
  205679. AMASYMMETRIC BASE
  205680. CATALYZED CYCLOADDITION BETWEEN ANTHRONE AND SOME DIENOPHILES
  205681. 1994 APR 11;50(15):4543
  205682. 4554X    4543-4554Y
  205683. 14926
  205684. Narasaka, K.B
  205685. Tetrahedron
  205686. CHIRAL TITANIUM REAGENT CATALYTIC ASYMMETRIC [2+2] CYCLOADDITION REACTION CATIONIC CYCLIZATION METHYLENECYCLOBUTANES CHIRAL TITANIUM REAGENT DIELS
  205687. ALDER REACTION CYCLOADDITION REACTION LEWIS
  205688. ACIDS 
  205689. SULFIDES 
  205690. DERIVATIVES 
  205691. THE CATALYTIC ASYMMETRIC [2+2] CYCLOADDITION PROCEEDS BETWEEN 3
  205692. ALKENOYL)
  205693. OXAZOLIDIN
  205694. ONES AND 1,2
  205695. PROPADIENYL SULFIDES HAVING VARIOUS SUBSTITUENTS AT 1
  205696. POSITION, AFFORDING METHYLENECYCLOBUTANE DERIVATIVES WITH HIGH OPTICAL PURITY. SEVEN AND EIGHT MEMBERED CARBOCYCLES WITH CHIRAL SIDE CHAINS ARE PREPARED BY THE RING CLEAVAGE REACTION AND SUCCESSIVE CATIONIC CYCLIZATION OF THE CHIRAL METHYLENECYCLOBUTANE DERIVATIVES HAVING w
  205697. ALKENYL SUBSTITUENTS.
  205698. 15935N
  205699. 2/28/96
  205700. AlASYMMETRIC SYNTHESIS OF METHYLENECYCLOBUTANES AND THEIR TRANSFORMATION TO MEDIUM
  205701. SIZED CARBOCYCLIC COMPOUNDS
  205702. 1994 APR 11;50(15):4529
  205703. 4542X    4529-4542Y
  205704. 14927
  205705. Doyle, M. P.B
  205706. TetrahedronCpSEMICORRIN METAL
  205707. COMPLEXES 
  205708. COPPER CARBENOID REACTION ASYMMETRIC
  205709. SYNTHESIS INSERTION REACTIONS LIGANDS 
  205710. OLEFINS 
  205711. DIAZODECOMPOSITION OF N
  205712. (TERT
  205713. BUTYL)
  205714. BUTEN
  205715. YL) DIAZOACETAMIDES CATALYZED BY DIRHODIUM(II) TETRAKIS[METHYL 2
  205716. PYRROLIDONE
  205717. CARBOXYLATE], RH
  205718. MEPY)(4), AND TETRAKIS [METHYL 2
  205719. OXAZOLIDINONE
  205720. 4(S) 
  205721. CARBOXYLATE], RH
  205722. MEOX)(4), FORMS PRODUCTS FROM INTRAMOLECULAR CYCLOPROPANATION IN GOOD YIELDS WITH ENANTIOMERIC EXCESSES RANGING FROM 60
  205723. 90%.  INTRAMOLECULAR CYCLOPROPANATION WITH N,N
  205724. DIALLYLDIAZOACETAMIDE (72% EE) IS COMPETITIVE WITH INTRAMOLECULAR [3+2] DIPOLAR CYCLOADDITION.
  205725. 15936N
  205726. 2/28/96
  205727. ENANTIOSELECTIVE INTRAMOLECULAR CYCLOPROPANATION OF N
  205728. ALLYLIC
  205729.  AND N
  205730. HOMOALLYLIC DIAZOACETAMIDES CATALYZED BY CHIRAL DIRHODIUM(II) CATALYSTS
  205731. 1994X    4519-4528Y
  205732. 14928
  205733. Pure Appl. Chem.M
  205734. 15937N
  205735. 2/28/96VENew approaches in asymmetric synthesis using gamma-alkoxybutenolides.X
  205736. 1865Y
  205737. GABRIEL WEATHERHEAD
  205738. 14929
  205739. Acc. Chem. Res.CCPHYSICAL ORGANIC /MECHANISMS /ELECTROPHILIC SUBSTITUTION /OXIDATIONM
  205740. 15938N
  205741. 2/28/96Vz1,3,5-Tris(dialkylamino)benzenes: model compounds for the electrophilic substitution and  oxidation of aromatic compounds.X
  205742. GABRIEL WEATHERHEAD
  205743. 14930
  205744. B5Progress in the Chemistry of Organic Natural Products
  205745. 15939N
  205746. 2/28/96V<Naturally occurring 6-substituted 5,6-dihydro-alpha-pyrones.X
  205747. GABRIEL WEATHERHEAD
  205748. 14931
  205749. B    SynthesisCOC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /PYRROLE /HETRING /5(N)M
  205750. 15940N
  205751. 2/28/96V5The Synthesis of 3-Substituted Pyrroles from Pyrrole.X
  205752. GABRIEL WEATHERHEAD
  205753. 14932
  205754. Angew. Chem., Int. Ed. Engl.C+REAGENTS /TiCl4 /TITANIUM TETRACHLORIDE /TiM
  205755. 15941N
  205756. 2/28/96V,Titanium Tetrachloride in Organic Synthesis.X
  205757. GABRIEL WEATHERHEAD
  205758. 14933
  205759. A truc, D.B
  205760. Acc. Chem. Res.M
  205761. 15942N
  205762. 2/28/96VFTransition-metal radicals: chameleon structure and catalytic function.W
  205763. 1991X
  205764. GABRIEL WEATHERHEAD
  205765. 14934
  205766. Chem. Soc. Rev.M
  205767. 15943N
  205768. 2/28/96VMMeldola Lecture - The Role Of Aromatic Interactions In Molecular  RecognitionW
  205769. 1994X
  205770. 101-109Y
  205771. GABRIEL WEATHERHEAD
  205772. 14935
  205773. Org. Prep. Proced. Int.M
  205774. 15944N
  205775. 2/28/96V6Homoenolates and other functionalized organometallics.W
  205776. GABRIEL WEATHERHEAD
  205777. 14936
  205778. Tetrahedron: AsymmetryM
  205779. 15945N
  205780. 2/28/96V:Asymmetric synthesis using homochiral lithium amide bases.W
  205781. 1991X
  205782. GABRIEL WEATHERHEAD
  205783. 14937
  205784. Acc. Chem. Res.M
  205785. 15946N
  205786. 2/28/96V
  205787. Metallabenzene chemistry.W
  205788. 1991X
  205789. GABRIEL WEATHERHEAD
  205790. 14938
  205791. Adv. Heterocycl. Chem.C
  205792. 15947N
  205793. 2/28/96V
  205794. 1,3-Thiazines.W
  205795. 1990X
  205796. GABRIEL WEATHERHEAD
  205797. 14939
  205798. Adv. Heterocycl. Chem.C
  205799. 15948N
  205800. 2/28/96V.Organocobalt-catalyzed synthesis of pyridines.W
  205801. 1990X
  205802. GABRIEL WEATHERHEAD
  205803. 14940
  205804. Angew. Chem., Int. Ed. Engl.C
  205805. 15949N
  205806. 2/28/96V8Cyclizations via palladium-catalyzed allylic alkylation.W
  205807. 1989X
  205808. 1173Y
  205809. GABRIEL WEATHERHEAD
  205810. 14941
  205811. TetrahedronC=FUNCTIONAL GROUPS /BIOTRANSFORMATIONS /ENZYMES /CARBOHYDRATESM
  205812. 15950N
  205813. 2/28/96V,Enzyme-Catalysed Synthesis of Carbohydrates.W
  205814. 1989X
  205815. 5365Y
  205816. GABRIEL WEATHERHEAD
  205817. 14942
  205818. Aldrichimica Acta
  205819. 15951N
  205820. 2/28/96V Rhodium-catalyzed hydroboration.W
  205821. 1989X
  205822. GABRIEL WEATHERHEAD
  205823. 14943
  205824. B    SynthesisC
  205825. C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /C-X /SO C-M(X) /Li(SO)  /SULFOXIDE /ALKYLATION CONJUGATE ADDITION /1,2-ADDITION /SM
  205826. 15952N
  205827. 2/28/96VUAsymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group.W
  205828. 1981X
  205829. GABRIEL WEATHERHEAD
  205830. 14944
  205831. Angew. Chem., Int. Ed. Engl.C-FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /C=CM
  205832. 15953N
  205833. 2/28/96V2Methods for the Preparation of Bridgehead Olefins.W
  205834. 1975X
  205835. GABRIEL WEATHERHEAD
  205836. 14945
  205837. Aldrichimica ActaCPREAGENTS /LITHIUM TRIETHYLBOROHYDRIDE /SUPER HYDRIDE /L-SELECTRIDE /REDUCTION /BM
  205838. 15954N
  205839. 2/28/96VKTrialkylborohydrides as New Versatile Reducing Agents in Oragnic Synthesis.W
  205840. 1974X
  205841. GABRIEL WEATHERHEAD
  205842. 14946
  205843. Adams, R. D.B
  205844. Chem. Soc. Rev.M
  205845. 15955N
  205846. 2/28/96
  205847. VlThe Insertion Of Alkynes Into Metal-Metal Bonds And Organic-Chemistry  Of The Dimetallated  Olefin ComplexesW
  205848. 1994X
  205849. 335-339Y
  205850. GABRIEL WEATHERHEAD
  205851. 14947
  205852. Adams, J.//Spero, D. M.B
  205853. TetrahedronC
  205854. 15956N
  205855. 2/28/96V<Rhodium(II) catalyzed reactions of diazo-carbonyl compounds.W
  205856. 1991X
  205857. 1765Y
  205858. GABRIEL WEATHERHEAD
  205859. 14948
  205860. Adams, R. D.B
  205861. Chem. Rev.C
  205862. ORGANOMETALLICS /GENERALM
  205863. 15957N
  205864. 2/28/96VJMetal cluster complexes containing heteroatom-substituted carbene ligands.W
  205865. 1989X
  205866. 1703Y
  205867. GABRIEL WEATHERHEAD
  205868. 14949
  205869. Adams, D. R.//Bhatnagar, S. D.B    SynthesisCxNAME REACTIONS /PRINS REACTION. /1,3-DIOXANES /HETRING /6(O,O) /DIOLS /1,3 /C-X(Y)  /Cl(O) /HETRING /6(O) /DIHYDROPYRANSM
  205870. 15958N
  205871. 2/28/96V
  205872. The Prins Reaction.W
  205873. 1977X
  205874. GABRIEL WEATHERHEAD
  205875. 14950
  205876. Adam, W.//Hadjiarapoglou, L.B
  205877. Top. Curr. Chem.M
  205878. 15959N
  205879. 2/28/96V*Dioxiranes: oxidation chemistry made easy.W
  205880. 1993X
  205881. GABRIEL WEATHERHEAD
  205882. 14951
  205883. A#Adam, W.//Curci, R.//Edwards, J. O.B
  205884. Acc. Chem. Res.CrFUNCTIONAL GROUPS /OXIDATION /ALKENES AND ALKYNES /MISCELLANEOUS /C=C /HETRING  /3(O,O) /DIOXIRANES /HETRING /3(O)M
  205885. 15960N
  205886. 2/28/96V-Dioxiranes: A New Class of Powerful Oxidants.W
  205887. 1989X
  205888. GABRIEL WEATHERHEAD
  205889. 14952
  205890. Adam, W.//Richter, M. J.B
  205891. Acc. Chem. Res.M
  205892. 15961N
  205893. 2/28/96V6Metal-catalyzed direct hydroxy-epoxidation of olefins.W
  205894. 1 94X
  205895. 57-62Y
  205896. GABRIEL WEATHERHEAD
  205897. 14953
  205898. Achiwa, K.B
  205899. HeterocyclesC
  205900. C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[3+2] /IMINES /IMIDATES  /THIOAMIDATES /IMIDINES /N-(SILYLMETHYL)IMINES /N-(SILYLMETHYL)AMINES /AZOMETHINE  YLIDES /THIOCARBONYL YLIDESM
  205901. 15962N
  205902. 2/28/96VYNew Generation of 1,3-Dipoles from Organosilicon Compounds and Synthesis of Heterocycles.W
  205903. 1988X
  205904. GABRIEL WEATHERHEAD
  205905. 14954
  205906. Acheson, R. M.B
  205907. Adv. Heterocycl. Chem.M
  205908. 15963N
  205909. 2/28/96V=1-Hydroxypyrroles, 1-hydroxyindoles, and 9-hydroxycarbazoles.W
  205910.  1990X
  205911. GABRIEL WEATHERHEAD
  205912. 14955
  205913. Abramovitch, R. A.B
  205914. Org. Prep. Proced. Int.M
  205915. 15964N
  205916. 2/28/96V6Applications of microwave energy in organic chemistry.W
  205917. 1991X
  205918. GABRIEL WEATHERHEAD
  205919. 14956
  205920. A2Abramovitch, R. A.//Barton, D. H. R.//Finet, J.-P.B
  205921. TetrahedronCHC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /ARYLATION /ARENESM
  205922. 15965N
  205923. 2/28/96V
  205924. New Methods of Arylation.W
  205925. 1988X
  205926. 3039Y
  205927. GABRIEL WEATHERHEAD
  205928. 14957
  205929. A%Abe, I.//Rohmer, M.//Prestwich, G. D.B
  205930. Chem. Rev.M
  205931. 15966N
  205932. 2/28/96VOEnzymatic cy lization of squalene and oxidosqualene to sterols and triterpenes.W
  205933. 1993X
  205934. 2189-206Y
  205935. GABRIEL WEATHERHEAD
  205936. 14958
  205937. Abdulla, R. F.B
  205938. Aldrichimica ActaC# TECHNIQUES AND METHODS /ULTRASOUNDM
  205939. 15967N
  205940. 2/28/96V Ultrasound in Organic Synthesis.W
  205941. 1988X
  205942. GABRIEL WEATHERHEAD
  205943. 14959
  205944. A!Abdulla, R. F.//Brinkmeyer, R. S.B
  205945. Tetrahedron
  205946. C[FUNCTIONAL GROUPS /PREPARATIONS /ETHERS AND ACETALS /C-X(Y)(Z) /N(O)(O)  /FORMAMIDE ACETALSM
  205947. 15968N
  205948. 2/28/96V#The Chemistry of Formamide Acetals.W
  205949. 1979X
  205950. 1675Y
  205951. GABRIEL WEATHERHEAD
  205952. 14960
  205953. A#Abdulganeva, S. A.//Erzhanov, K. B.B Russ. Che . Rev. (Engl. Transl.)M
  205954. 15969N
  205955. 2/28/96V
  205956. Acetylenic amino acids.W
  205957. 1991X
  205958. GABRIEL WEATHERHEAD
  205959. 14961
  205960. A1Abboud, J. M.//Notario, R.//Bertran, J.//Sola, M.B
  205961. Prog. Phys. Org. Chem.M
  205962. 15970N
  205963. 2/28/96VCOne century of physical organic chemistry: The Menshutkin reaction.W
  205964. 1993X
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  205968. 15971N
  205969. 2/28/96VdInvestigations on the Arbuzov and retro-Arbuzov reactions among the organic derivatives of  arsenic.W
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  205972. GABRIEL WEATHERHEAD
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  205975. Adv. Phys. Org. Chem.CfPHYSICAL ORGANIC /REARRANGEMENTS /REACTIVE INTERMEDIATES /CARBONIUM IONS  CARBOCATIONS /REARRANGEMENTS
  205976. 15972N
  205977. 2/28/96V&Degenerate Carbocation Rearrangements.W
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  205979. GABRIEL WEATHERHEAD
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  205981. Aguero, A.//Osborn, J. A.B
  205982. New Journal of ChemistryC
  205983. ORGANOMETALLICS /GENERALM
  205984. 15973N
  205985. 2/28/96V/Synthesis routes to metal-alkylidene complexes.W
  205986. 1988X
  205987. GABRIEL WEATHERHEAD
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  205989. AZAgrofoglio, L.//Suhas, E.//Farese, A.//Condom, R.//Challand, S. R.//Earl, R. A.  Guedj, R.B
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  205992. 2/28/96V$Synthesis Of Carbocyclic NucleosidesW
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  205995. GABRIEL WEATHERHEAD
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  205997. Aggarwal, V. K.B
  205998. Angew. Chem., Int. Ed. Engl.C
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  206000. 2/28/96VmEnantioselective transformations and racemization studies of heteroatom substituted organolithium  compounds.W
  206001. 1994X
  206002. 175-7Y
  206003. GABRIEL WEATHERHEAD
  206004. 14967
  206005. Ager, D. J.//East, M. B.B
  206006. TetrahedronM
  206007. 15976N
  206008. 2/28/96VBThe synthesis of carbohydrate derivatives from acyclic precursors.W
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  206010. 5683-765Y
  206011. GABRIEL WEATHERHEAD
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  206013. Ager, D. J.//East, M. B.B
  206014. Tetra edronM
  206015. 15977N
  206016. 2/28/96VeMethodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate  derivatives.W
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  206019. GABRIEL WEATHERHEAD
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  206021. Ager, D. J.B
  206022. Org. React. (N.Y.)CdORGANOMETALLICS /SILICON /FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /C-M(M')  /Li(Si),Si(Sn) /C=C /SiM
  206023. 15978N
  206024. 2/28/96V"The Peterson olefination reaction.W
  206025. 1990X
  206026. GABRIEL WEATHERHEAD
  206027. 14970
  206028. Ager, D. J.B    SynthesisC
  206029. FUNCT ONAL GROUPS /PREPARATIONS /ALKENES /O=C-H /O=C-R /M-C-C-X /Si,OH /PETERSON /C=C  /ALKENES /C=C-X /S /C=C-C=O /C=C-C=C /SiM
  206030. 15979N
  206031. 2/28/96V
  206032. The Peterson Reaction.W
  206033. 1984X
  206034. GABRIEL WEATHERHEAD
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  206036. A    Agami, C.B
  206037. Bull. Soc. Chim. Fr.C
  206038. C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /1,2-ADDITION /O=C-H  /ALKEHYDES /O=C-R /KETONES /PROLINE /ALDOL /ENANTIOSELECTIVEM
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  206040. 2/28/96VUMechanism of the Proline-Catalysed Enantioselective Aldol Reaction - Recent Advances.W
  206041. GABRIEL WEATHERHEAD
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  206043. A7Afarinkia, K.//Vinader, V.//Nelson, T. D.//Posner, . H.B
  206044. TetrahedronM
  206045. 15981N
  206046. 2/28/96V8Diels-Alder cycloadditions of 2-pyrones and 2-pyridones.W
  206047. 1992X
  206048. 9111Y
  206049. GABRIEL WEATHERHEAD
  206050. 14973
  206051. Afarinkia, K.B
  206052. HeterocyclesC
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  206054. 2/28/96VNFour-membered heterocycles containing one phosphorus and one other heteroatom.W
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  206056. GABRIEL WEATHERHEAD
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  206058. Adkins, H.B
  206059. Org. React. (N Y.)M
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  206061. 2/28/96V.Catalytic Hydrogenation of Esters to Alcohols.W
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  206063. GABRIEL WEATHERHEAD
  206064. 14975
  206065. AMAder, U.//Andersch, P.//Berger, M.//Goergens, U.//Seemayer, R.//Schneider, M.B
  206066. Pure Appl. Chem.M
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  206068. 2/28/96VPHydrolases in organic synthesis: preparation of enantiomerically pure compounds.W
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  206071. GABRIEL WEATHERHEAD
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  206073. adekov, I. D.//Minkin, V. I.B
  206074. Adv. Heterocycl. Chem.C
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  206076. 2/28/96V7Tellurium-containing heterocycles with two heteroatoms.W
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  206078. GABRIEL WEATHERHEAD
  206079. 14977
  206080. A$Addlington, R. M.//Barrett, A. G. M.B
  206081. Acc. Chem. Res.C
  206082. FUNCT ONAL GROUPS /PREPARATIONS /ALKENES /BuLi /KETONES ARYLSULPHONYLHYDRAZONES  /TOSYLHYDRAZONES /C=N-X /NH2-SO2 /SHAPIRO REACTION /BAMFORD-STEVENS REACTION  /C=C-M /LiM
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  206084. 2/28/96V,Recent Applications of the Shapiro Reaction.W
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  206086. GABRIEL WEATHERHEAD
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  206088. All n, G. R.B
  206089. Org. React. (N.Y.)CLC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /NENITZESCU /INDOLESM
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  206091. 2/28/96V=The Synthesis of 5-Hydroxyindoles by the Nenitzescu Reaction.W
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  206093. GABRIEL WEATHERHEAD
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  206098. 2/28/96VHKinetics and mechanism of oxidation of organoelement compounds by ozone.W
  206099. 1982X
  206100. GABRIEL WEATHERHEAD
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  206102. Alexandrov, Y. A.B
  206103. J. Organomet. Chem.
  206104. C8ORGANOMETALLICS /SILICON /ORGANOSILICON PEROXIDES /Si /OM
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  206106. 2/28/96V6Preparation and properties of organosilicon peroxides.W
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  206108. GABRIEL WEATHERHEAD
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  206110. Alexakis, A.B
  206111. Pure Appl. Chem.M
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  206113. 2/28/96V_Stereochemical aspects of the formation of chiral allenes from propargyli  ethers and epoxides.W
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  206115. GABRIEL WEATHERHEAD
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  206117. Alexakis, A.//Mangeney, P.B
  206118. Tetrahedron: AsymmetryC
  206119. C-C BOND FORMATION /APPENDAGES /DIASTEREOGENIC REACTIONS /FUNCTIONAL GROUPS  /PREPARATIONS /ETHERS AND ACETALS /C=C-C-X(Y) /O(O) /C-X(Y)M
  206120. 15991N
  206121. 2/28/96V'Chiral acetals in asymmetric synthesis.W
  206122. 1990X
  206123. GABRIEL WEATHERHEAD
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  206126. Pure Appl. Chem.C
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  206130. VXChiral Acetals in Enantio- and Diastereoselective Substitution or Elimination Reactions.W
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  206137. 2/28/96VYOrganocopper Reagents for the Synthesis of Saturated and Ethylenic Aldehydes and Ketones.W
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  206139. GABRIEL WEATHERHEAD
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  206142. Pure Appl. Chem.CUORGANOMETALLICS /COPPER /CC-C-X(Y) /O(O) /CARBOMETALLATION /Cu /O=C-C=C  /O=C-C=C-C=CM
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  206144. 2/28/96VzCarbocupration of Acetylenic Acetals and Ketals: Synthesis of alpha, beta-Ethylenic Acetals, and of  Dienals and Dienones.W
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  206150. 15995N
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  206152. VTReactions of pyridines, pyrimidines, and 1,3,5-triazines with nucleophilic reagents.W
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  206158. 2/28/96V>Spiropyrans. Structural features and photochemical properties.W
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  206160. GABRIEL WEATHERHEAD
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  206163. TetrahedronC
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  206165. 15997N
  206166. 2/28/96V
  206167. Intrabridgehead Chemistry.W
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  206174. 2/28/96V!Strain Effects in Amine Basicity.W
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  206180. TetrahedronC
  206181. C-C BOND FORMATION /APPENDAGES /SYN /C-M(X)(Y) /Li(CN)(O) /ACYL ANION EQUIVALENT  /CYANOHYDRINS /DIALKYLAMINONITRILES /ALKYLATION /O=C-R /KETONESM
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  206183. 2/28/96
  206184. VoReactions of Acyl Anion Equivalents Derived from Cyanohydrins, Protected Cy nohydrins and Dialkylaminonitriles.W
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  206187. GABRIEL WEATHERHEAD
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  206189. Albright, T. A.B
  206190. TetrahedronC
  206191. ORGANOMETALLICS /GENERAL /C-MM
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  206193. 2/28/96V\Structure and Reactivity in Organometallic Chemistry. An Applied Molecular Orbital Approach.W
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  206196. GABRIEL WEATHERHEAD
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  206201. 2/28/96VJThe synthesis of stable, isolable planar-tetracoordinate carbon compounds.W
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  206208. 16002N
  206209. 2/28/96V
  206210. A new method in radical chemistry: generation of radicals by photo-induced electron transfer and  fragmentation of the radical cation.W
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  206213. GABRIEL WEATHERHEAD
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  206216. Top. Curr. Chem.M
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  206218. 2/28/96V$PET-Reactions of aromatic c mpounds.W
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  206220. GABRIEL WEATHERHEAD
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  206222. Albini, A.B    SynthesisM
  206223. 16004N
  206224. 2/28/96V$Synthetic utility of amine N-oxides.W
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  206227. GABRIEL WEATHERHEAD
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  206232. 2/28/96V,Synthesis of Peptides with Mixed Anhydrides.W
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  206239. 2/28/96VbRuthenium and osmium complexes containing cyclopentadienyl and related pentahapto-dienyl  lignads.W
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  206244. Coord. Chem. Rev.C2ORGANOMETALLICS /G NERAL /METAL CARBONYL COMPLEXESM
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  206246. 2/28/96VQReagent and catalysts induced substitution reactions of metal carbonyl complexes.W
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  206248. GABRIEL WEATHERHEAD
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  206251. Org. Prep. Proced. Int.M
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  206254. VARecent advances in the use of acylium salts in organic synthesis.W
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  206262. GABRIEL WEATHERHEAD
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  206265. CHEMTECHC%FUNCTIONAL GROUPS /BIOTRANSFORMATIONSM
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  206268. Enzymes in organic synthesis.W
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  206270. GABRIEL WEATHERHEAD
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  206275. 2/28/96VjA unified mechanistic view of oxidative reactions catalyzed by P-450 and related iron-containing  enzymes.W
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  206282. VZThe synthesis and properties of N-(2,3-epoxypropyl)carbazoles and oligomers based on them.W
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  206286. Akelah, A.B    SynthesisCHODDS AND ENDS /TECHNIQUES AND METHODS /POLYMERS /HETEROGENEOUS SYNTHESISM
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  206288. 2/28/96V>Heterogeneous Organic Synthesis Using Functionalised Polymers.W
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  206295. 2/28/96V
  206296. The Sommelet Reaction.W
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  206303. 2/28/96V6Dynamics of Eight-Membered Rings in Cyclooctane Class.W
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  206323. 2/28/96V+Electrophilic aminations with oxaziridines.W
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  206325. GABRIEL WEATHERHEAD
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  206330. 2/28/96V"Heteroaromatic-fused 3-sulfolenes.W
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  206336. Acc. Chem. Res.C`PHYS CAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /YLIDE /CARBENES /YLIDES  /REARRANGEMENT /SM
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  206338. 2/28/96V\Ylide Formation and Rearrangement in the Reaction of Carbene with Divalent Sulfur Compounds.W
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  206345. 2/28/96V+Expanding roles for templates in synthesis.W
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  206347. GABRIEL WEATHERHEAD
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  206351. 2/28/96V0Synthetic Applications of Chlorotrimethylsilane.W
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  206355. Anderson, J. E.B
  206356. Top. Curr. Chem.C/PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATIONM
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  206358. 2/28/96V3Chair-Chair Interconversions of Six-Membered Rings.W
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  206365. 2/28/96V Chemistry at diplatinum centers.W
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  206372. GABRIEL WEATHERHEAD
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  206386. 2/28/96V"Bis- and Oligo(benzocrown ether)s.W
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  206394. 2/28/96V9Macropolycyclic polyethers (cages) and related compounds.W
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  206401. 2/28/96V+The Chemical Synthesis of Oligonucleotides.W
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  206405. Amarnath, V.//Matlhav, R.B    SynthesisCFC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETRING /6(N)M
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  206407. 2/28/96V>A Survey of Methods for the Preparation of Pyrrolopyrimidines.W
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  206409. GABRIEL WEATHERHEAD
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  206411. Alvarez, M.//Joule, J. A.B
  206412. HeterocyclesM
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  206414. 2/28/96V
  206415. Synthesis of pyridoacridines.W
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  206421. HeterocyclesM
  206422. 16032N
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  206427. 15024
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  206429. HeterocyclesM
  206430. 16033N
  206431. 2/28/96V
  206432. Marine, nitrogen-containing heterocyclic natural products. Str ctures and syntheses of compounds containing quinoline and /or isoquinoline units.W
  206433. 1991X
  206434. GABRIEL WEATHERHEAD
  206435. 15025
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  206437. Aldrichimica ActaM
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  206439. 2/28/96VaSimple,  ovel methods for the synthesis of carbonyl compounds using metal complexes as catalysts.W
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  206441. GABRIEL WEATHERHEAD
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  206444. J. Organomet. Chem.CGORGANOMETALLICS /ORGANIC SYNTHESIS /CARBONYLATION INSERTION /Co /Rh /PdM
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  206446. 2/28/96V@Homogenous and phase transfer catalysed carbonylation reactions.W
  206447. 1986X
  206448. GABRIEL WEATHERHEAD
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  206451. Adv. Organomet. Chem.CoODDS AND ENDS /TECHNIQUES AND METHODS /PHASE TRANSFER /ORGANOMETALLICS /GENERAL  /PHASE TRANSFER CATALYSIS /PTCM
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  206453. 2/28/96V5Phase Transfer Catalysis in Organometallic Chemistry.W
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  206459. 2/28/96VAFunctionalization of the dihydrothiazine ring of cephem sulfones.W
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  206467. 2/28/96V@2-(Heteroatom-substituted)methyl penems. IV. Oxygen derivatives.W
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  206474. 2/28/96VC2-(Heteroatom-substituted)methyl penems. III. Nitrogen deriv tives.W
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  206480. Pure Appl. Chem.C/PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATIONM
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  206482. 2/28/96V%On the Conformation of Lactone Rings.W
  206483. 1982X
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  206485. GABRIEL WEATHERHEAD
  206486. 15032
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  206491. Furanosesquiterpene synthesis.W
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  206505. 2/28/96V~Hydrozirconation-isomerization. Reactions of terminally functionalized olefins with zirconocene  hydrides and general aspects.W
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  206527. 2/28/96VNAdditions of Aliphatic and Aromatic Acyl Isocyanates to Unsaturated Compounds.W
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  206529. GABRIEL WEATHERHEAD
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  206534. 2/28/96VCCycloaddition Reactions of Aliphatic and Aromatic Aryl Isocyanides.W
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  206536. GABRIEL WEATHERHEAD
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  206558. 2/28/96VBPhotochemical one-way adiabatic isomerization of aromatic olefins.W
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  206565. 2/28/96V%Polycyclic Aromatic Nitrogen Cations.W
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  206573. 2/28/96VkTertiary Phosphane /Tetrachloromethane, a Versatile Reagent for Chlorination, Dehydration, and  RN Linkage.W
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  206585. 2/28/96V)Oxidation of Olefins with Mercuric Salts.W
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  206591. 2/28/96VFCarbon-carbon bond formation in electron-deficient aromatic compounds.W
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  206604. Org. React. (N.Y.)CgC-C BOND FORMATION /APPENDAGES /ENOLATES /C-M(X) /Li(CN) /C=C=X-M /N-Li /NITRILES  /ALKYLATION /C-X /CNM
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  206606. 2/28/96VEAddition and Substitution Reactions of Nitrile-Stabilised Carbanions.W
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  206608. GABRIEL WEATHERHEAD
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  206613. 2/28/96V0Preparation and reactions of indolin-2(3H)-ones.W
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  206633. 2/28/96V%Low-Coordinate Hypervalent PhosphorusW
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  206635. GABRIEL WEATHERHEAD
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  206641. The transformation of aromatics into regio-and stereocontrolled heterobifunctional  cyclohexadienes mediated by temporary sandwich complexation.Roles of electron,proton,hydride and  hydrogen-atom transfersW
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  206656. 2/28/96VGOrgano-Iron Complexes of Aromatic Compounds. Applications in Synthesis.W
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  206663. 2/28/96VJBacterial lipids containing amino acids or peptides linked by amide bonds.W
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  206692. 2/28/96VVA Detailed Description of the Mechanism of Reaction of Grignard Reagents with Ketones.W
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  206701. The Composition of Grignard Compounds in Ether Solvents as Inferred from Molecular Association  and NMR Studies. The Relevance of Grignard Composition to Reaction Mechanism and Stereochemistry.W
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  206722. 2/28/96V4Double-calixarene design, synthesis, and properties.W
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  206738. 2/28/96V9Synthesis of condensed thiazolo[3,2-a] yrimidine systems.W
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  206753. 2/28/96V$Steric Interactions of Double Bonds.W
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  206769. 2/28/96VCThe Oxidation of Organic Nitrogen Compounds with Lead Tetraacetate.W
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  206775. 2/28/96V%Aminoacids of the cyclobutane series.W
  206776. 1993X
  206777. GABRIEL WEATHERHEAD
  206778. 15072
  206779. UADAvalos, M.//Babiano, R.//Cintas, P.//Jimenez, J. L.//Palacios, J. C.B
  206780. HeterocyclesM
  206781. 16081N
  206782. 2/28/96VSHaloalkyl isothiocyanates, useful and versatile reage ts in heterocyclic chemistry.W
  206783. 1992X
  206784. GABRIEL WEATHERHEAD
  206785. 15073
  206786. Aurich, H. G.B
  206787. Pure Appl. Chem.C
  206788. FUNCTIONAL GROUPS /PREPARATIONSM
  206789. 16082N
  206790. 2/28/96V"The chemistry of vinyl nitroxides.W
  206791. 1990X
  206792. GABRIEL WEATHERHEAD
  206793. 15074
  206794. Auner, N.//Ziche, W.//West, R.B
  206795. Heteroatom ChemistryC
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  206797. 2/28/96V/The won erful world of organosilicon chemistry.W
  206798. 1991X
  206799. GABRIEL WEATHERHEAD
  206800. 15075
  206801. Atwell, W. H.//Weyenberg, D. R.B
  206802. Angew. Chem., Int. Ed. Engl.C
  206803. ORGANOMETALLICS /SILICON /SiM
  206804. 16084N
  206805. 2/28/96V
  206806. Divalent Silicon Intermediates.W
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  206808. GABRIEL WEATHERHEAD
  206809. 15076
  206810. YA5Attwood, J. D.//Wovkulich, M. J.//Sonnenberger, O. C.B
  206811. Acc. Chem. Res.C+ORGANOMETALLICS /GENERAL /C-M /SUBSTITUTIONM
  206812. 16085N
  206813. 2/28/96V8Ligand Effects in Organometallic Substitution Reactions.W
  206814. 1983X
  206815. GABRIEL WEATHERHEAD
  206816. 15077
  206817. Astruc, D.B
  206818. New Journal of ChemistryC
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  206820. 2/28/96V
  206821. Transition metal sandwiches as reservoirs of electrons, protons, hydro en atoms and hydrides: molecular activation and electronics.W
  206822. 1992X
  206823. 305-28Y
  206824. GABRIEL WEATHERHEAD
  206825. 15078
  206826. Back, T. G.B
  206827. TetrahedronC;TARGET SYNTHESIS /MACROLIDES /NATURAL PRODUCTS /ANTIBIOTICSM
  206828. 16087N
  206829. 2/28/96VSThe Synthesis of Macrocyclic Lactones. Approaches to Complex Macrolide Antibiotics.W
  206830. 1977X
  206831. 3041Y
  206832. GABRIEL WEATHERHEAD
  206833. 15079
  206834. Baciocchi, E.B
  206835. Acc. Chem. Res.C-PHYSICAL ORGANIC /MECHANISMS /ELIMINATION /E2M
  206836. 16088N
  206837. 2/28/96VMBase Dependence of Transition-State Structure in Alkene-Forming E2 Reactions.W
  206838. 1979X
  206839. GABRIEL WEATHERHEAD
  206840. 15080
  206841. Bachmann, W. E.//Hoffman, R. A.B
  206842. Org. React. (N.Y.)M
  206843. 16089N
  206844. 2/28/96VaThe Preparation of Unsymmetrical Biaryls by the Diazo Reaction and the Nitroacetylamine Reaction.W
  206845. 1944X
  206846. GABRIEL WEATHERHEAD
  206847. 15081
  206848. Bachmann, W. E.//Struve, W. S.B
  206849. Org. React. (N.Y.)M
  206850. 16090N
  206851. 2/28/96V
  206852. The Arndt-Eistert Reaction.W
  206853. 1942X
  206854. GABRIEL WEATHERHEAD
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  206856. _ARBachi, M. D.//Balanov, A.//Bar-Ner, N.//Bosch, E.//Denenmark, D.//Mizhiritskii, M.B
  206857. Pure Appl. Chem.M
  206858. 16091N
  206859. 2/28/96VOSynthesis of nonaromatic heterocyclic compounds through free-radical reactions.W
  206860. 1993X
  206861. 595-6 1Y
  206862. GABRIEL WEATHERHEAD
  206863. 15083
  206864. Bach, T.B
  206865. Angew. Chem., Int. Ed. Engl.M
  206866. 16092N
  206867. 2/28/96
  206868. `VVCatalytic enantioselective C-C coupling - allyl transfer and Mukaiyama aldol reaction.W
  206869. 1994X
  206870. 417-19Y
  206871. GABRIEL WEATHERHEAD
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  206876. 2/28/96VXThe Mechanism of the Lithium - Halogen Interchange Reaction: A Review of the Literature.W
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  206878. GABRIEL WEATHERHEAD
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  206880. Bailey, C. L.//rago, R. S.B
  206881. Coord. Chem. Rev.CzORGANOMETALLICS /COBALT /FUNCTIONAL GROUPS /ALKENES AND ALKYNES /C=C /OXIDATION  /C-OH /O=C-H /O=C-R /DICARBONYLS /1,2 /CoM
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  206883. 2/28/96V]Utilisation of Oxygen for the Specific Oxidation of Organic Substrates with Co(II) Catalysts.W
  206884. 1987X
  206885. GABRIEL WEATHERHEAD
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  206890. The introduction of functional groups into unsaturated systems by carbonyl compounds in the  presence of manganese(III) acetate.W
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  206892. GABRIEL WEATHERHEAD
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  206895. Pure Appl. Chem.C
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  206897. 2/28/96VFPalladium-catalyzed intramolecular 1,4-additions to conjugated dienes.W
  206898. 1992X
  206899. GABRIEL WEATHERHEAD
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  206902. New Journal of ChemistryM
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  206904. 2/28/96V>Stereoselective annulations via palladium-catalyzed reactions.W
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  206906. GABRIEL WEATHERHEAD
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  206909. Acc. Chem. Res.C)ORGANOMETALLICS /PALLADIUM /OXIDATION /PdM
  206910. 16098N
  206911. 2/28/96V0Palladium in Some Selective Oxidation Reactions.W
  206912. 1983X
  206913. GABRIEL WEATHERHEAD
  206914. 15090
  206915. Baldwin, J. E., Ed.B
  206916. Tetrahedron Symposium-in-PrintC9TARGET SYNTHESIS /MISCELLANEOUS /
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  206918. 16099N
  206919. 2/28/96V-Recent Aspects of the Chemistry of 
  206920. -Lactams.W
  206921. 1983X
  206922. 2445Y
  206923. GABRIEL WEATHERHEAD
  206924. 15091
  206925. Balch, A. L.B
  206926. Pure Appl. Chem.M
  206927. 16100N
  206928. 2/28/96VoMetallomacrocycles: novel amphoteric macrocycles with metal ions and traditional Lewis bases as  binding sites.W
  206929. 1988X
  206930. GABRIEL WEATHERHEAD
  206931. 15092
  206932. Balaram, P.B
  206933. Pure Appl. Chem.M
  206934. 16101N
  206935. 2/28/96V8The design and construction of synthetic protein mimics.W
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  206937. 1061Y
  206938. GABRIEL WEATHERHEAD
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  206940. Balaban, A. T.B
  206941. Pure Appl. Chem.M
  206942. 16102N
  206943. 2/28/96VHBenzenoid catafusenes: perfect matchings, isomerization, automerization.W
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  206945. GABRIEL WEATHERHEAD
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  206947. Baker, R.//Swain, C. J.B    Chem. Br.C
  206948. TARGET SYNTHESIS /IVERMECTINM
  206949. 16103N
  206950. 2/28/96V$Ivermectin - a Drug for All Seasons.W
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  206952. GABRIEL WEATHERHEAD
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  206954. Baker, R.//Herbert, R. H.B
  206955. Nat. Prod. Rep.C
  206956. TARGET SYNTHESIS /PHEROMONESM
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  206958. 2/28/96V/Insect Pheromones and Related Natural Products.W
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  206960. GABRIEL WEATHERHEAD
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  206962. mA    Baker, R.B
  206963. Chem. Rev.
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  206966. 2/28/96V. -Allylmetal Derivatives in Organic Synthesis.W
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  206968. GABRIEL WEATHERHEAD
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  206971. TetrahedronCKFUNCTIONAL GROUPS /TRANSFORMATIONS /ELECTROCHEMICAL REACTIONS /ELECTROLYSISM
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  206973. 2/28/96V9Recent Developments in Organic Synthesis by Electrolysis.W
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  206975. GABRIEL WEATHERHEAD
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  206978. Prog. Phys. Org. Chem.CcC-C BOND FORMATION /APPENDAGES /ELECTROCHEMISTRY /ELECTROCHEMICAL /ELECTROLYTIC  REDUCTIVE COUPLINGM
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  206980. 2/28/96VCElectrolytic Reductive Coupling: Synthetic and Mechanistic Aspects.W
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  206983. GABRIEL WEATHERHEAD
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  206986. Top. Curr. Chem.C9FUNCTIONAL GROUPS /TRANSFORMATIONS /CYCLOPROPANE CLEAVAGEM
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  206988. 2/28/96V8Functionalized cyclopropenes as synthetic intermediates.W
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  206990. GABRIEL WEATHERHEAD
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  206992. qA7Barluenga, J.//Joglar, J.//Gonzalez, F. J.//Fustero, S.B
  206993. SynlettCXC-C BOND FORMATION /HETEROANNULATIONS /6-RING /C=N-C=C /CYCLOADDITION /[4+2]  /N-C-C-C-OM
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  206995. 2/28/96V\Electronically Neutral 2-Aza-1,3-dienes: Are They Useful Intermediates in Organic Synthesis?W
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  206997. GABRIEL WEATHERHEAD
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  206999. rA0Barluenga, J.//Aznar, F.//Fustero, S.//Tomas, M.B
  207000. Pure Appl. Chem.M
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  207002. 2/28/96VENew perspectives of carbo and hetero-1,3-dienes in organic synthesis.W
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  207004. 1957Y
  207005. GABRIEL WEATHERHEAD
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  207007. Barluenga, J.B
  207008. Pure Appl. Chem.C
  207009. ORGANOMETALLICS /LITHIUM  LiM
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  207011. 2/28/96VcPreparation and some applications of functionalized organo-lithium compounds in organic  synthesis.W
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  207013. GABRIEL WEATHERHEAD
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  207016. Chem. Rev.C6PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /HgM
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  207018. 2/28/96V+Free Radical Reactions of Organomercurials.W
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  207020. GABRIEL WEATHERHEAD
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  207024. 2/28/96V]Steroids with a side chain containing a heterocyclic fragment: synthesis and transformations.W
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  207029. 16114N
  207030. 2/28/96V+Aliphatic organophosphorus nitro-compounds.W
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  207033. GABRIEL WEATHERHEAD
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  207036. Aust. J. Chem.M
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  207038. 2/28/96V5New methods for the synthesis of troponoid compounds.W
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  207040. GABRIEL WEATHERHEAD
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  207043. TetrahedronM
  207044. 16116N
  207045. 2/28/96V
  207046. Anellated HeterophospholesW
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  207048. GABRIEL WEATHERHEAD
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  207053. 2/28/96V8Synthesis of oligosaccharides of 2-amino-2-deoxy sugars.W
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  207056. GABRIEL WEATHERHEAD
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  207060. 2/28/96V.Dithiadiazoles: a new family of free radicals.W
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  207062. GABRIEL WEATHERHEAD
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  207064. Banfi, L.//Guanti, G.B    SynthesisM
  207065. 16119N
  207066. 2/28/96VcAsymmetrized 2-methyl-1,3-propanediol and its equivalents: preparation and synthetic  applications.W
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  207069. GABRIEL WEATHERHEAD
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  207074. 2/28/96VtMethods for angular alkoxycarbonylation in fused rings and its application to the synthesis of  terpenoid compounds.W
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  207076. GABRIEL WEATHERHEAD
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  207078. Bally, T.//Masamune, S.B
  207079. TetrahedronC1TARGET SYNTHESIS /UNNATURAL PRODUCTS /CARBRING /4M
  207080. 16121N
  207081. 2/28/96V
  207082. Cyclobutadiene.W
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  207084. GABRIEL WEATHERHEAD
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  207089. 2/28/96VLPerchloro-organic chemistry: Structures, spectroscopy and reaction pathways.W
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  207094. Angew. Chem., Int. Ed. Engl.C.TARGET SYNTHESIS /PROSTAGLANDINS /LEUKOTRIENESM
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  207097. Prostaglandins.W
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  207099. GABRIEL WEATHERHEAD
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  207104. 2/28/96V]Stereocontrol in the Synthesis of Acyclic Systems: Applications to Natural Product Synthesis.W
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  207106. GABRIEL WEATHERHEAD
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  207111. 2/28/96V$Delocalized Carbanions in Synthesis.W
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  207113. GABRIEL WEATHERHEAD
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  207118. 2/28/96V4Recent studies on the Peterson olefination reaction.W
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  207120. GABRIEL WEATHERHEAD
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  207123. Chem. Soc. Rev.C8C-C BOND FORMATION /APPENDAGES /1,4-ADDITION /C=C-X /NO2M
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  207125. 2/28/96V,Heterosubstituted nitroalkenes in synthesis.
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  207127. GABRIEL WEATHERHEAD
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  207130. TetrahedronC:FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /C=C-X /NO2M
  207131. 16128N
  207132. 2/28/96V+Nitroalkanes and Nitroalkenes in Synthesis.W
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  207135. GABRIEL WEATHERHEAD
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  207140. 2/28/96V>Applications of organometallic reagents in 
  207141. -lactam chemistry.W
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  207144. GABRIEL WEATHERHEAD
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  207149. 2/28/96VFConjugated Nitroalkenes: Versatile Intermediates in Organic Synthesis.W
  207150. 1986X
  207151. GABRIEL WEATHERHEAD
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  207154. Heteroatom ChemistryC
  207155. Si /Ge /Fe /Ru /CoM
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  207157. 2/28/96VfRecent developments in heterocyclic systems with a Si-M'-Ge or Ge-M'-Ge linkage (M' = Fe, Ru,  or Co).W
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  207164. 2/28/96V7Multiply bonded germanium species. Recent developments.W
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  207166. GABRIEL WEATHERHEAD
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  207170. 16133N
  207171. 2/28/96V)Synthesis of heterocycles from azadienes.W
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  207174. GABRIEL WEATHERHEAD
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  207179. 2/28/96VRSynthesis and reactivity of lambda5-phosphazenes. Uses as synthetic intermediates.W
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  207181. GABRIEL WEATHERHEAD
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  207186. 2/28/96V$Cation-Radical Pericyclic Reactions.W
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  207188. GABRIEL WEATHERHEAD
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  207191. Angew. Chem., Int. Ed. Engl.ClFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /O=C-X /NH-OH /HYDROXAMIC ACIDS  /HYDROXYIMIDES /O=C-X /NH-OHM
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  207193. 2/28/96
  207194. V6The Chemistry of Hydroxamic Acids and N-Hydroxyimides.W
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  207201. 2/28/96V/Open-Chain Polyphosphorus Hydrides (phosphanes)W
  207202. 1994X    1273-1297Y
  207203. GABRIEL WEATHERHEAD
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  207208. 2/28/96VXContributions to the chemistry of phosphorus. 218. Monocyclic and polycyclic phosphines.W
  207209. 1993X
  207210. 1623-67Y
  207211. GABRIEL WEATHERHEAD
  207212. 15130
  207213. Baschang, G.M
  207214. 16139N
  207215. 2/28/96VCMuramyl peptides and lipopeptides: studies towards immunostimulantsW
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  207217. GABRIEL WEATHERHEAD
  207218. 15131
  207219. Basavaiah, D.//Krishna, P. R.B
  207220. Pure Appl. Chem.M
  207221. 16140N
  207222. 2/28/96V/Enantioselective synthesis using crude enzymes.W
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  207225. GABRIEL WEATHERHEAD
  207226. 15132
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  207228. Chem. Rev.CLPHYSICAL ORGANIC /MECHANISMS /STEREOCHEMISTRY /ELIMINATION /E2 /ALKENES /C=CM
  207229. 16141N
  207230. 2/28/96
  207231. VFStereochemical and Base Dichotomies in Olefin-Forming E2 Eliminations.W
  207232. 1980X
  207233. GABRIEL WEATHERHEAD
  207234. 15133
  207235. Bartsch, R. A.B
  207236. Acc. Chem. Res.C7PHYSICAL ORGANIC /MECHANISMS /ELIMINATION /C=C /ALK NESM
  207237. 16142N
  207238. 2/28/96V;Ionic Association in Base-Promoted 
  207239. -Elimination Reactions.W
  207240. 1975X
  207241. GABRIEL WEATHERHEAD
  207242. 15134
  207243. Barton, D. H. R.//Parekh, S. I.B
  207244. Pure Appl. Chem.M
  207245. 16143N
  207246. 2/28/96V.Ligand coupling based on heteroatom chemistry.W
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  207249. GABRIEL WEATHERHEAD
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  207252. Acc. Chem. Res.M
  207253. 16144N
  207254. 2/28/96VIThe selective functionalization of saturated hydrocarbons: Gif chemistry.W
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  207256. GABRIEL WEATHERHEAD
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  207259. Top. Stereochem.C2ODDS AND ENDS /HISTORY AND BIOGRAPHY /CONFORMATIONM
  207260. 16145N
  207261. 2/28/96VXConformational Analysis. The Fundamental Contributions of D. H. R. Barton and O. Hassel.W
  207262. 1971X
  207263. GABRIEL WEATHERHEAD
  207264. 15137
  207265. Bartoli, G.B
  207266. Acc. Chem. Res.C|C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE /ORGANOMETALLICS /MAGNESIUM /Ar-X  /NO2 /C-M /Mg /CONJUGATE /1,4-ADDITION /MgM
  207267. 16146N
  207268. 2/28/96VAConjugate Addition of Alkyl Grignard Reagents to Mononitroarenes.W
  207269. 1984X
  207270. GABRIEL WEATHERHEAD
  207271. 15138
  207272. Becher, J.//Stidsen, C. E.B
  207273. Sulfur ReportsM
  207274. 16147N
  207275. 2/28/96VcRecent developments in the synthesis and chemistry of 2(1H)-pyridinethiones and related  compounds.W
  207276. 1988X
  207277. GABRIEL WEATHERHEAD
  207278. 15139
  207279. Beaucage, S. L.//Iyer, R. P.B
  207280. TetrahedronM
  207281. 16148N
  207282. 2/28/96VsThe synthesis of specific ribonucleotides and unrelated phosphorylated biomolecules by the  phosphoramidite method.W
  207283. 1993X
  207284. 10441-88Y
  207285. GABRIEL WEATHERHEAD
  207286. 15140
  207287. Beaucage, S. L.//Iyer, R. P.B
  207288. TetrahedronM
  207289. 16149N
  207290. 2/28/96VbThe synthesis of modified oligonucleotides by the phosphoramidite approach and their applications.W
  207291. 1993X
  207292. 6123-94Y
  207293. GABRIEL WEATHERHEAD
  207294. 15141
  207295. Beaucage, S. L.//Iyer, R. P.B
  207296. TetrahedronM
  207297. 16150N
  207298. 2/28/96VJThe functionalization of oligon cleotides via phosphoramidite derivatives.W
  207299. 1993X
  207300. 1925-63Y
  207301. GABRIEL WEATHERHEAD
  207302. 15142
  207303. Beaucage, S. L.//Iyer, R. P.B
  207304. TetrahedronCHTARGET SYNTHESIS /MISCELLANEOUS /FUNCTIONAL GROUPS /PROTECTION /HYDROXYLM
  207305. 16151N
  207306. 2/28/96VNAdvances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach.W
  207307. 1992X
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  207309. GABRIEL WEATHERHEAD
  207310. 15143
  207311. Beak, P.M
  207312. 16152N
  207313. 2/28/96W
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  207315. GABRIEL WEATHERHEAD
  207316. 15144
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  207318. Acc. Chem. Res.M
  207319. 16153N
  207320. 2/28/96V
  207321. Determinations of transition-state geometries by the endocyclic restriction test: mechanisms of  substitution at nonstereogenic atoms.W
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  207323. GABRIEL WEATHERHEAD
  207324. 15145
  207325. Beak, P.//Meyers, A. I.B
  207326. Acc. Chem. Res.COORGANOMETALLICS /MAGNESIUM /ZINC /STEREOCHEMISTRY /CARBOMETALLATION /Li /Mg /ZnM
  207327. 16154N
  207328. 2/28/96
  207329. VeStereo- and Regiocontrol by Complex Induced Proximity Effects: Reactions of Organolithium  Compounds.W
  207330. 1986X
  207331. GABRIEL WEATHERHEAD
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  207333. A%Beak, P.//Zajdel, W. J.//Reitz, D. B.B
  207334. Chem. Rev.M
  207335. 16155N
  207336. 2/28/96V
  207337. Metalation and Electrophilic Substitution of Amine Derivatives Adjavcent to Nitrogen:  alpha-Metallo Amine Synthetic Equivalents.W
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  207339. GABRIEL WEATHERHEAD
  207340. 15147
  207341. Beak, P.//Reitz, D. B.B
  207342. Chem. Rev.C4PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBANIONSM
  207343. 16156N
  207344. 2/28/96V=Dipole-Stabilized Carbanions: Novel and Useful Intermediates.W
  207345. 1978X
  207346. GABRIEL WEATHERHEAD
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  207349. Acc. Chem. Res.CkC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /AROMATIC AMIDES  /METALLATION /Li /Ar-M /Li /X-C=C-MM
  207350. 16157N
  207351. 2/28/96VqDirected Lithiation of Aromatic Teriary Amides: An Evolving Synthetic Methodology for  Polysubstituted Aromatics.W
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  207355. A    Bayer, E.B
  207356. Angew. Chem., Int. Ed. Engl.M
  207357. 16158N
  207358. 2/28/96V*Toward the chemical synthesis of proteins.W
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  207360. GABRIEL WEATHERHEAD
  207361. 15150
  207362. Bauslaugh, P. G.B    SynthesisC
  207363. C-C BOND FORMATION /ANNULATIONS /4-RING /PHOTOCHEMICAL REACTIONS /C=C-C=O /ENONES  /C=C /ALKENES /PHOTOCHEMICAL CYCLOADDITION /[2+2]M
  207364. 16159N
  207365. 2/28/96VSPhotochemical Cycloaddition Reactions of Enones to Alkenes: Synthetic Applications.W
  207366. 1970X
  207367. GABRIEL WEATHERHEAD
  207368. 15151
  207369. Bauld, N. L.B
  207370. TetrahedronC
  207371. PHYSICAL ORGANIC /C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2]  /SIGMATROPIC /REACTIVE INTERMEDIATES /CATION RADICAL /ANNULATION /3, 4, 6-RING  /REARRANGEMENT /RING EXPANSION /4 TO 6, 3 TO 5 /CARBRING /4M
  207372. 16160N
  207373. 2/28/96V@Cation Radical Cycloadditions and Related Sigmatropic Reactions.W
  207374. 1989X
  207375. 5307Y
  207376. GABRIEL WEATHERHEAD
  207377. 15152
  207378. Becker, K. B.B    SynthesisCAC-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE /STILBENES /ARENESM
  207379. 16161N
  207380. 2/28/96
  207381. Synthesis of Stilbenes.W
  207382. 1983X
  207383. GABRIEL WEATHERHEAD
  207384. 15153
  207385. Becker, K.B
  207386. TetrahedronC
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  207388. 16162N
  207389. 2/28/96V/Cycloalkenes by Intramolecular Wittig Reaction.W
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  207391. 1717Y
  207392. GABRIEL WEATHERHEAD
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  207394. Beck, J. R.B
  207395. Tetrahedr nCYC-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE /Ar-X /NO2 /NITRO /SUBSTITUTION  /NO2 BY CM
  207396. 16163N
  207397. 2/28/96V3Nucleophilic Displacement of Aromatic Nitro Groups.W
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  207404. 16164N
  207405. 2/28/96V}The Cross Coupling Reactions of Organic Halides with Organic Derivatives of Tin, Mercury, and  Copper Catalysed by Palladium.W
  207406. 1983X
  207407. GABRIEL WEATHERHEAD
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  207410. Org. React. (N.Y.)C
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  207412. 16165N
  207413. 2/28/96VZThe Persulfate Oxidation of Phenols and Arylamines (The Elbs and Boyland-Sims Oxidations).W
  207414. 1987X
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  207419. FUNCTIONAL GROUPS /TRANSFORMAT ONS /C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /HETRING /3(O) /EPOXIDES  /OXIRANES /EPOXYALCOHOLS /SHARPLESS /EPOXIDE CLEAVAGE /REDUCTION /DIOLS /1,2 /DIOLS  /1,3M
  207420. 16166N
  207421. 2/28/96ViNew Transformations of 2,3-Epoxy Alcohols and Related Derivatives. Easy Routes to Homochiral  Substances.W
  207422. 1983X
  207423. GABRIEL WEATHERHEAD
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  207425. Begue, J. P.//Bonnet-Delpon, D.B
  207426. TetrahedronC.FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUSM
  207427. 16167N
  207428. 2/28/96VGPreparation of trifluoromethyl ketones and related fluorinated ketones.W
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  207444. 2/28/96V0The pursuit of selectivity in radical reactions.W
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  207450. TetrahedronCT PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /STEREOCHEMISTRY /REGIOCHEMISTRYM
  207451. 16170N
  207452. 2/28/96V<Regioselectivity and Stereoselectivity in Radical Reactions.W
  207453. 1981X
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  207455. GABRIEL WEATHERHEAD
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  207457. Benz, H.B    SynthesisM
  207458. 16171N
  207459. 2/28/96VJThe role of solid-phase fragment condensation (SPFC) in peptide synthesis.W
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  207467. 2/28/96V3
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  207474. Pure Appl. Chem.M
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  207476. 2/28/96VXThe stabilization and reactivity of strained cyclic alkynes on transition metal centers.W
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  207483. 16174N
  207484. 2/28/96V1Metal Complexes of Small Cycloalkynes and Arynes.W
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  207488. Bennett, G. B.B    SynthesisCLC-C BOND FORMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[3,3] /NAME REACTIONSM
  207489. 16175N
  207490. 2/28/96V/The Claisen Rearrangement in Organic Synthesis.W
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  207497. 2/28/96VZUnusual electrophilic substitution in the aromatic series via organosilicon intermediates.W
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  207505. 2/28/96V8Stereospecificity in Enzymology: Its Place in Evolution.W
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  207507. GABRIEL WEATHERHEAD
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  207510. HeterocyclesCLTARGET SYNTHESIS /ALKALOIDS /HETEROCYCLES /N-ALKYLPYRIDINIUM SALTS /ADDITIONM
  207511. 16178N
  207512. 2/28/96VkAddition of Stabilised Carbon Nucleophiles to N-Alkylpyridinium Salts. Applications to Alkaloid  Synthesis.W
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  207516. Benkeser, R. A.B    SynthesisC'ORGANOMETALLICS /MAGNESIUM /C=C-C-M /MgM
  207517. 16179N
  207518. 2/28/96V4The Chemistry of Allyl and Crotyl Grignard Reagents.W
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  207520. GABRIEL WEATHERHEAD
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  207523. HeterocyclesM
  207524. 16180N
  207525. 2/28/96V?Reactions of 2,6- diaryl-3,7-dioxabicyclo[3.3.0]octane lignans.W
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  207533. 2/28/96V;Synthesis, Structure And Mechanism In Immunophilin ResearchW
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  207540. 16182N
  207541. 2/28/96V
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  207547. Pure Appl. Chem.M
  207548. 16183N
  207549. 2/28/96V6Synthesis of new torands and new uses for old torands.W
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  207556. 16184N
  207557. 2/28/96VANitrile imines: from matrix characterization to stable compounds.W
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  207560. GABRIEL WEATHERHEAD
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  207563. Heteroatom ChemistryC
  207564. 16185N
  207565. 2/28/96VsBis(diisopropylamino)phosphinyldiazomethane: a building block for the syn hesis of stable carbene and nitrilimines.W
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  207570. Top. Stereochem.CAC-C BOND FORMATION /HETEROANNULATIONS /3-RING /EPOXIDES /OXIRANESM
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  207572. 2/28/96V8Stereochemical Aspects of the Synthesis of 1,2-Epoxides.W
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  207574. GABRIEL WEATHERHEAD
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  207577. Acc. Chem. Res.M
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  207580. The overlap component of the stereoelectronic factor. Remote control of stereogenicity transfer  through the anisotropic influence of a ring.W
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  207582. GABRIEL WEATHERHEAD
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  207585. Chemtracts: Organic ChemistryM
  207586. 16188N
  207587. 2/28/96V
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  207590. GABRIEL WEATHERHEAD
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  207594. 16189N
  207595. 2/28/96V8Recent advances in the synthesis of achiral carotenoids.W
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  207600. Angew. Chem., Int. Ed. Engl.C
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  207602. 2/28/96V,Classical a d nonclassical methyleneboranes.W
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  207605. GABRIEL WEATHERHEAD
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  207608. TetrahedronCAPHYSICAL ORGANIC /MECHANISMS /C=C /ALKENES /NUCLEOPHILIC ADDITIONM
  207609. 16191N
  207610. 2/28/96V9Nucleophilic Addition to Olefins. Kinetics and Mechanism.W
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  207616. Acc. Chem. Res.M
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  207618. 2/28/96VnPredicting forbidden and allowed cycloaddition reactions: potential surface topology and its  rationalization.W
  207619. 1990X
  207620. GABRIEL WEATHERHEAD
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  207622. Berliner, E.B
  207623. Org. Re ct. (N.Y.)M
  207624. 16193N
  207625. 2/28/96VFThe Friedel and Crafts Reaction with Aliphatic Dibasic Acid Anydrides.W
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  207627. GABRIEL WEATHERHEAD
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  207629. A(Bergmann, E. D.//Ginsburg, D.//Pappo, R.B
  207630. Org. React. (N.Y.)M
  207631. 16194N
  207632. 2/28/96V
  207633. The Michael Reaction.W
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  207635. GABRIEL WEATHERHEAD
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  207637. Bergman, J.//Pelcman, B.B
  207638. Pure Appl. Chem.M
  207639. 16195N
  207640. 2/28/96V!Synthesis of carbazole alkaloids.W
  207641. 1990X
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  207643. GABRIEL WEATHERHEAD
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  207645. A[Berger, B.//De Raadt, A.//Griengl, H.//Hayden, W.//Hechtberger, P.//Klempier, N.//Faber, K.B
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  207647. 16196N
  207648. 2/28/96V=Useful hydrolytic enzymes: proteases, lipases and nitrilases.W
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  207651. GABRIEL WEATHERHEAD
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  207653. ANBergatrom, D.//Lin, X.//Wang, G.//Rotstein, D.//Beal, P.//Norrix, K.//Ruth, J.B
  207654. SynlettM
  207655. 16197N
  207656. 2/28/96V#C-5 Substituted nucleoside analogs.W
  207657. 1992X
  207658. GABRIEL WEATHERHEAD
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  207660. Bickelhaupt, F.B
  207661. Acta Chem. Scand.C
  207662. 16198N
  207663. 2/28/96VJThe importance of (intramolecular) solvation in organomagnesium chemistry.W
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  207666. GABRIEL WEATHERHEAD
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  207668. Bickelhaupt, F.
  207669. Pure Appl. Chem.C!ORGANOMETALLICS /GENERAL /C-M(M')M
  207670. 16199N
  207671. 2/28/96V"New trends in dimetallic synthons.W
  207672. 1990X
  207673. GABRIEL WEATHERHEAD
  207674. 15191
  207675. Bickelhaupt, F.B
  207676. Pure Appl. Chem.M
  207677. 16200N
  207678. 2/28/96V-Small cyclophanes: the bent benzene business.W
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  207680. GABRIEL WEATHERHEAD
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  207682. Bickelhaupt, F.//De Wolf, W. H.B
  207683. Recl. Trav  Chim. Pays-BasM
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  207685. 2/28/96V3Bridged valence isomers of benzene and cyclophanes.W
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  207687. GABRIEL WEATHERHEAD
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  207690. Angew. Chem., Int. Ed. Engl.CuC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[3+2] /CYCLOREVERSIONS  /1,3-DIPOLAR /CYCLOREVERSION /[3+2]M
  207691. 16202N
  207692. 2/28/96V
  207693. 1,3-Dipolar Cycloreversions.W
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  207695. GABRIEL WEATHERHEAD
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  207697. Bhatt, M. V.//Kulkarni, S. U.B    Synthesis
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  207701. Cleavage of Ethers.W
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  207703. GABRIEL WEATHERHEAD
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  207707. 2/28/96V
  207708. Forskolin and congeners.W
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  207711. GABRIEL WEATHERHEAD
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  207714. Acc. Chem. Res.CSPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /ION RADICALS /CARBENE ION RADICALS /C=N=NM
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  207716. 2/28/96VsIn Search of Carbene Ion Ra icals in Solution: Reaction Pathways and Reactivity of Ion Radicals of Diazo Compounds.W
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  207718. GABRIEL WEATHERHEAD
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  207721. Pure Appl. Chem.M
  207722. 16206N
  207723. 2/28/96VBSyntheses and reactions of mono- and polyelementorganic compounds.W
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  207729. Top. Curr. Chem.
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  207732. 2/28/96VLSelected Topics of the Wittig Reaction in the Synthesis of Natural Products.W
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  207734. GABRIEL WEATHERHEAD
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  207736. Bestmann, H. J.B
  207737. Angew. Chem., Int. Ed. Engl.CPFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /ORGANOMETALLICS /PHOSPHORUS /YLIDES /PM
  207738. 16208N
  207739. 2/28/96V1Phosphacumulene Ylides and Phospha-alkene Ylides.W
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  207741. GABRIEL WEATHERHEAD
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  207744. Angew. Chem., Int. Ed. Engl.C
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  207747. 2/28/96VDNew Reactions of Alkylidienephosphoranes and Their Preparative Uses.W
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  207749. GABRIEL WEATHERHEAD
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  207751. Besse, P.//Veschambre, H.B
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  207754. 2/28/96V4Chemical And Biolog cal Synthesis Of Chiral EpoxidesW
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  207756. GABRIEL WEATHERHEAD
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  207770. 2/28/96V9Homogeneous Hydrogenation Catalysts in Organic Synthesis.W
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  207784. Acc. Chem. Res.CSC-C BOND FORMATION /ANNULATIONS /3-RING /CYCLOPROPENES /CARBRING /3  /CYCLOPROPENESM
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  207786. 2/28/96V.Synthesis and Chemistry of Benzocyclopropenes.W
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  207794. 2/28/96V@Recent Developments in the Synthesis of myo-Inositol Phosphates.W
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  207799. Chem. Soc. Rev.C$ORGANOMETALLICS /NICKEL /C=C-C-M /NiM
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  207801. 2/28/96VB -Allyl Nickel Halides as Selective Reagents in Organic Synthesis.W
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  207806. Adv. Carbohydr. Chem. Biochem.M
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  207808. 2/28/96VIHydrolysis and other cleavages of glycosidic linkages in polysaccharides.W
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  207810. GABRIEL WEATHERHEAD
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  207813. Org. React. (N.Y.)C
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  207815. 16218N
  207816. 2/28/96V;Allylic and Benzylic Carbanions Substitut d by Heteroatoms.W
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  207818. GABRIEL WEATHERHEAD
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  207820. Biehl, E. R.//Khanapure, S. P.B
  207821. Acc. Chem. Res.CyC-C BOND FORMATION /AROMATICS /RING FORMATION /CHAIN APPENDAGE /C-M(X)(Y)  /Li(CN)(O) /ARYNES /ANNULATION /6-RING /ARENESM
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  207823. 2/28/96V7Synthesis of Polycyclics via Aryne Arylation Reactions.W
  207824. 1989X
  207825. GABRIEL WEATHERHEAD
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  207827. Bickelhaupt, .B
  207828. Pure Appl. Chem.C
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  207830. 2/28/96VCCarbenoid routes to substituted phosphaalkenes and phosphabenzenes.W
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  207833. GABRIEL WEATHERHEAD
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  207835. Blagoev, B.//Ivanov, D.B    SynthesisC1C-C BOND FORMATION /APPENDAGES /ENOLATES /C-M /MgM
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  207837. 2/28/96V8Syntheses with Polyfunctional Organomagnesium Compounds.W
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  207839. GABRIEL WEATHERHEAD
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  207844. 2/28/96VUStoichiometric applications of organotransition metal complexes in organic synthesis.W
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  207851. 2/28/96VhApplication of phosphonate and thiophosphate analogs of nucleoti es to studies of some enzyme reactions.W
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  207853. GABRIEL WEATHERHEAD
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  207855. A=Blackburn, B. K.//Davies, S. G.//Sutton, K. H.//Whittaker, M.B
  207856. Chem. Soc. Rev.C
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  207858. 16224N
  207859. 2/28/96VvA Conformational Analysis of Transition Metal eta-1-Acyl Complexes: Steric Interactions and  Stereoel ctronic Effects.W
  207860. 1988X
  207861. GABRIEL WEATHERHEAD
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  207863. Black, D. S. C.B
  207864. SynlettM
  207865. 16225N
  207866. 2/28/96VKNew dimensions in indole chemistry: from ligand design to natural products.W
  207867. 1993X
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  207869. GABRIEL WEATHERHEAD
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  207871. Black, T. H.B
  207872. Aldrichimica ActaC
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  207875. 2/28/96
  207876. V.The Preparation and Reactions of Diazomethane.W
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  207878. GABRIEL WEATHERHEAD
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  207880. Bishop III, K. C.B
  207881. Chem. Rev.C1ORGANOMETALLICS /GENERAL /REARRANGEMENTS /C-M  TMM
  207882. 16227N
  207883. 2/28/96VITransition Metal Catalysed Rearrangement of Small Ring Organic Molecules.W
  207884. 1976X
  207885. GABRIEL WEATHERHEAD
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  207887. Birkofer, L.//Stuhl, O.M
  207888. 16228N
  207889. 2/28/96V
  207890. Silylated Synthons.W
  207891. 1980a
  207892. GABRIEL WEATHERHEAD
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  207894. A    Block, E.B
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  207897. 2/28/96VaThe organosulfur chemistry of the genus Allium: implications for the organic chemistry of sulfur.W
  207898. 1992a
  207899. GABRIEL WEATHERHEAD
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  207901. Block, E.//Aslam, M.B
  207902. TetrahedronC
  207903. ORGANOMETALLICS /SILICON /Si /SM
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  207905. 2/28/96V5The Chemistry of Mixed  rganosulfur-Silicon CompoundsW
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  207907. GABRIEL WEATHERHEAD
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  207909. A    Block, E.B
  207910. Org. React. (N.Y.)CHFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /DIOLS /1,2 /DEOXYGENATION /C=CM
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  207912. 2/28/96
  207913. V4Olefin Synthesis via Deoxygenation of Vicinal Diols.W
  207914. 1984X
  207915. GABRIEL WEATHERHEAD
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  207917. A    Block, E.B
  207918. Aldrichimica ActaC
  207919. 16232N
  207920. 2/28/96VDOrganic Sulfur Compounds in Organic Synthesis: Some Recent Advances.W
  207921. 1978X
  207922. GABRIEL WEATHERHEAD
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  207924. Blizzard, T. A.B
  207925. Org. Prep. Proced. Int.M
  207926. 16233N
  207927. 2/28/96VKRecent Progress In The Synthesis Of Avermectins And Milbemycins - A  ReviewW
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  207930. GABRIEL WEATHERHEAD
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  207932. Blicke, F. F.B
  207933. Org. React. (N.Y.)M
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  207935. 2/28/96V
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  207937. 1942X
  207938. GABRIEL WEATHERHEAD
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  207942. 2/28/96a
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  207945. Blechert, S.B    SynthesisCXC-C BOND FORMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[3,3] /HETERO-COPE  REARRANGEMENTM
  207946. 16236N
  207947. 2/28/96V3The Hetero-Cope Rearrangement in Organic Synthesis.W
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  207949. GABRIEL WEATHERHEAD
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  207951. A;Blazevic, N.//Kolbah, D.//Belin, B.//Sunjic, V.//Kajfez, F.B    SynthesisC7REAGENTS /HEXAMETHYLENETETRAMINE /AMINATION FORMYLATIONM
  207952. 16237N
  207953. 2/28/96VAHexamethylenetetramine, A Versatile Reagent in Organic Synthesis.W
  207954. 1979X
  207955. GABRIEL WEATHERHEAD
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  207957. Blatt, A. H.B
  207958. Org. React. (N.Y.)M
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  207960. 2/28/96V
  207961. The Fries Reaction.W
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  207963. GABRIEL WEATHERHEAD
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  207965. Blasko, G.//Cordell, G. A.B
  207966. HeterocyclesCOTARGET SYNTHESIS /ALKALOIDS /PSCHORR PHOTOCYCLISATION PHENOL OXIDATIVE COUPLINGM
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  207968. 2/28/96V
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  207977. 2/28/96VJThe chiral pool as a source of enantioselective catalysts and auxiliaries.W
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  207979. GABRIEL WEATHERHEAD
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  207981. Blaser, H. U.B
  207982. Tetrahedron: AsymmetryM
  207983. 16241N
  207984. 2/28/96V@Enantioselective synthesis using chira  heterogeneous catalysts.W
  207985. 1991X
  207986. GABRIEL WEATHERHEAD
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  207988. Boczon, W.
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  207990. 16242N
  207991. 2/28/96VDStereochemical aspects of bisquinolizidine alkaloids sparteine type.W
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  207994. GABRIEL WEATHERHEAD
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  207996. Bock, H.B
  207997. Angew. Chem., Int. Ed. Engl.C
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  207999. 2/28/96VTFundamentals of silicon chemistry. Molecular states of silicon-containing compounds.W
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  208004. A    Boche, G.B
  208005. Angew. Chem., Int. Ed. Engl.C
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  208008. 2/28/96V
  208009. The Structure of Lithium Coumpounds of Sulfones, Sulfoximides, Sulfoxides, Thioethers, 1,3  Dithianes, Nitriles, Nitro Compounds, and Hydrazones.W
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  208011. GABRIEL WEATHERHEAD
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  208013. A    Boch , G.B
  208014. Top. Curr. Chem.CDPHYSICAL ORGANIC /REARRANGEMENTS /REACTIVE INTERMEDIATES /CARBANIONSM
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  208016. 2/28/96
  208017. Rearrangements of carbanions.W
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  208019. GABRIEL WEATHERHEAD
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  208021. A Bobbitt, J. M.//Flores, M. C. C.B
  208022. HeterocyclesC&REAGENTS /NITROSONIUM SALTS /OXIDATIONM
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  208024. 2/28/96V;Organic Nitrosonium Salts as Oxidants in Organic Chemistry.W
  208025. 1988X
  208026. GABRIEL WEATHERHEAD
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  208028. Bobbit , J. M.//Bourque, A. J.B
  208029. HeterocyclesC
  208030. C-C BOND FORMATION /HETEROANNULATIONS /AMINOACETALS /HETEROCYCLES /ISOQUINOLINES  /PYRAZINES /PYRROLES /INDOLES /AZEPINES /DIAZEPINES /IMIDAZOLES /OXAZOLES /THIAZOLESM
  208031. 16247N
  208032. 2/28/96V-Synthesis of Heterocycles Using Aminoacetals.W
  208033. 1987X
  208034. GABRIEL WEATHERHEAD
  208035. 15239
  208036. A+Boa, A. N.//Jenkins, P. R.//Lawrence, N. J.B
  208037. Contemporary Organic SynthesisM
  208038. 16248N
  208039. 2/28/96V,Recent progress in the synthesis of taxanes.W
  208040. 1994X
  208041. GABRIEL WEATHERHEAD
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  208043. Blystone, S. L.B
  208044. Chem. Rev.C>ORGANOMETALLICS /ORGANIC SYNTHESIS /Pd /Cu /Zn /Au /Fe /Re /MoM
  208045. 16249N
  208046. 2/28/96
  208047. VUSynthetic applications of enantioselective organotransition-metal-mediated reactions.W
  208048. 1989X
  208049. 1663Y
  208050. GABRIEL WEATHERHEAD
  208051. 15241
  208052. A+Blunden, S. J.//Cusack, P. A.//Smith, P. J.B
  208053. J. Organomet.  hem.C5TARGET SYNTHESIS /NUCLEOSIDES /TIN /CARBOHYDRATES /SnM
  208054. 16250N
  208055. 2/28/96VBThe use of tin compounds in carbohydrate and nucleoside chemistry.W
  208056. 1987X
  208057. GABRIEL WEATHERHEAD
  208058. 15242
  208059. Blumenkopf, T.//Overman, L. E.B
  208060. Chem. Rev.C^C-C BOND FORMATION /MISCELLANEOUS /ORGANOMETALLICS /SILICON /ANNULATION /ALKENES  /ALLENES /SiM
  208061. 16251N
  208062. 2/28/96V?Vinylsilane-and Alkynylsilane-Terminated Cyclisation Reactions.W
  208063. 1986X
  208064. GABRIEL WEATHERHEAD
  208065. 15243
  208066. A.Bloomfield, J. J.//Owsley, D. C.//Nelke, J. M.B
  208067. Org. React. (N.Y.)M
  208068. 16252N
  208069. 2/28/96V
  208070. The Acyloin Condensation.W
  208071. 1976X
  208072. GABRIEL WEATHERHEAD
  208073. 15244
  208074. Blomberg, C.//Hartog, F. H.B    SynthesisC
  208075. ORGANOMETALLICS /MAGNESIUM /MgM
  208076. 16253N
  208077. 2/28/96
  208078. VXThe Barbier Reaction-A One Step Alternative for Syntheses via Organomagnesium Compounds.W
  208079. 1977X
  208080. GABRIEL WEATHERHEAD
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  208082. Boger, . L.B
  208083. Chemtracts: Organic ChemistryM
  208084. 16254N
  208085. 2/28/96VTDuocarmycins - a new class of sequence selective DNA minor groove alkylating agents.W
  208086. 1991X
  208087. GABRIEL WEATHERHEAD
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  208089. Boger, D. L.B
  208090. TetrahedronCRC-C BOND FORMATION /HETEROANNULATIONS /6-RING /AZADIENES /DIELS-ALDER REACTION /DAM
  208091. 16255N
  208092. 2/28/96V#Diels-Alder Reactions of Azadienes.W
  208093. 1983X
  208094. 2869Y
  208095. GABRIEL WEATHERHEAD
  208096. 15247
  208097. Bogdanovic, B.M
  208098. 16256N
  208099. 2/28/96W
  208100. 1985a
  208101. GABRIEL WEATHERHEAD
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  208103. AIBogdanovic, B.//Henc, B.//Losler, A.//Meister, B.//Pauling, H.//Wilke, G.B
  208104. Angew. Chem., Int. Ed. Engl.CaC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /ORGANOMETALLICS  /SYNTHESIS /TM CATALYSTSM
  208105. 16257N
  208106. 2/28/96VLAsymmetric Synthesis with the Aid of Homogeneous Transition Metal Catalysts.W
  208107. 1973X
  208108. GABRIEL WEATHERHEAD
  208109. 15249
  208110. Boehmer, V.//Vogt, W.B
  208111. Pure Appl. Chem.M
  208112. 16258N
  208113. 2/28/96V)Calix[4]arenes, bridged at the upper rim.W
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  208116. GABRIEL WEATHERHEAD
  208117. 15250
  208118. Bodanszky, M.//Martinez, J.B    SynthesisC)TARGET SYNTHESIS /MISCELLANEOUS /PEPTIDESM
  208119. 16259N
  208120. 2/28/96V$Side Reactions in Peptide Synthesis.W
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  208124. Bonnemann, H.B
  208125. Angew. Chem., Int. Ed. Engl.CeC-C BOND FORMATION /AROMATICS /RING FORMATION /ORGANOMETALLICS /COBALT /PYRIDINES  /HETRING /6(N) /CoM
  208126. 16260N
  208127. 2/28/96V
  208128. Organocobalt Compounds in the Synthesis of Pyridines. An Example of Structure-Effectivity  Relationships in Homogeneous Catalysis.W
  208129. 1985X
  208130. GABRIEL WEATHERHEAD
  208131. 15252
  208132.     ACBonnemann, H.//Grard, C.//Kopp, W.//Pump, W.//Tanaka, K.  Wilke, G.B
  208133. Angew. Chem., Int. Ed. Engl.C$ORGANOMETALLICS /COBALT /C=C-C-M /CoM
  208134. 16261N
  208135. 2/28/96V
  208136. The Allylcobalt System.W
  208137. 1973X
  208138. GABRIEL WEATHERHEAD
  208139. 15253
  208140. Bonnemann, H.//Brijoux, WM
  208141. 16262N
  208142. 2/28/96a
  208143. GABRIEL WEATHERHEAD
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  208146. 16263N
  208147. 2/28/96V^Regio- and chemoselective synthesis of halohydrins by cleavage of oxiranes with metal halides.W
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  208150. GABRIEL WEATHERHEAD
  208151. 15255
  208152. Bolm, C.B
  208153. Angew. Chem., Int. Ed. Engl.C
  208154. 16264N
  208155. 2/28/96VaEnantioselective transition metal-catalyzed hydrogenation for the asymmetric synthesis of amines.W
  208156. 1993X
  208157. GABRIEL WEATHERHEAD
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  208160. 16265N
  208161. 2/28/96V7Esterolytic and lip lytic enzymes in organic synthesis.W
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  208164. GABRIEL WEATHERHEAD
  208165. 15257
  208166. Boivin, T. L. B.B
  208167. TetrahedronC
  208168. TARGET SYNTHESIS /MACROLIDES /C-C BOND FORMATION /HETEROANNULATIONS /6-RING  5-RING /MISCELLANEOUS /SPIROACETALS  HETRING /6(O) HETRING /5(O) /TETRAHYDROFURANS  /TETRAHYDROPYRANS /THF /THPM
  208169. 16266N
  208170. 2/28/96
  208171. Synthetic Routes to Tetrahydrofuran, Tetrahydropyran, and Spiroacetal Units of Polyether  Antibiotics and a Survey of Spiroketals of Other Natural Products.W
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  208174. GABRIEL WEATHERHEAD
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  208178. 16267N
  208179. 2/28/96V
  208180. PAH [polycyclic aromatic hydrocarbons] and fullerene ions and ion/molecule reactions in  interstellar and circumstellar chemistry.W
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  208187. 16268N
  208188. 2/28/96V8The folding of squalene: an old problem has new results.W
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  208190. GABRIEL WEATHERHEAD
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  208193. 16269N
  208194. 2/28/96VbSelective replacement of hydrogen at a saturated carbon atom under the action of oxidizing agents.W
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  208198. A9Botteghi, C.//Paganelli, S.//Schionato, A.//Marchetti, M.B    ChiralityM
  208199. 16270N
  208200. 2/28/96
  208201. V@Asymmetric hydroformylation in the synthesis of pharmaceuticals.W
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  208203. GABRIEL WEATHERHEAD
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  208205. Borthwick, A. D.//Biggadike, K.B
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  208207. 16271N
  208208. 2/28/96V,Synthesis of chiral carbocyclic nucleosides.W
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  208212. A]Borovkov, V. V.//Evst gneeva, R. P.//Strekova, L. N.//Filippovich, E. I.//Khairutdinov, R. F.B Russ. Chem. Rev. (Engl. Transl.)M
  208213. 16272N
  208214. 2/28/96VYPorphyrin-quinone compounds as synthetic models of the reaction center in photosynthesis.W
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  208216. GABRIEL WEATHERHEAD
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  208218. Bordwell, F. G.//Zhang, X.-M.B
  208219. Acc. Chem. Res.M
  208220. 16273N
  208221. 2/28/96V=From equilibrium acidities to radical stabilization energies.W
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  208224. GABRIEL WEATHERHEAD
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  208226. Bordwell, F. G.B
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  208228. 16274N
  208229. 2/28/96V9How Common Are Base-Initiated Concerted 1,2-Eliminations?W
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  208231. GABRIEL WEATHERHEAD
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  208233. Bordwell, F. G.B
  208234. Acc. Chem. Res.C8PHYSICAL ORGANIC /MECHANISMS /SUBSTITUTION /NUCLEOPHILICM
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  208236. 2/28/96VUAre Nucleophilic Bimolecular Concerted Reactions Involving Four or More Bonds a Myth?W
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  208240. Borden, W. T.B
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  208243. 2/28/96V
  208244. Pyramidalised Alkenes.W
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  208247. GABRIEL WEATHERHEAD
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  208249. ABBoraldi, P. G.//Barco, A.//Baretti, S.//Bollini, G. P.//Simoni, D.B    SynthesisCTC-C BOND FORMATION /ANNULATIONS /6-RING /TARGET SYNTHESIS /MISCELLANEOUS  /ISOXAZOLEM
  208250. 16277N
  208251. 2/28/96V-Synthesis of Natural Products via Isoxazoles.W
  208252. 1987X
  208253. GABRIEL WEATHERHEAD
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  208255. Boone, J. R.B
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  208257. 16278N
  208258. 2/28/96VDReductions of Cyclic and Bicyclic Ketones by Complex Metal Hydrides.W
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  208265. 16279N
  208266. 2/28/96V5Olefin Synthesis with Organic Phosphonate Carbanions.W
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  208268. GABRIEL WEATHERHEAD
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  208270. A/Bradshaw, J. S.//Krakowiak, K. E.//Izatt, R. M.B
  208271. TetrahedronM
  208272. 16280N
  208273. 2/28/96V-Preparation of diamino ethers and polyamines.W
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  208287. Box, V. G. S.B
  208288. HeterocyclesM
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  208290. 2/28/96V
  208291. The significance of the bond lengths and bond orders of conjugated unsaturated organic molecules.  The role of hetero-aromaticity in the tertiary structures  f DNA.W
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  208296. Box, V. G. S.B
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  208299. 2/28/96
  208300. The relationship between bond type, bond order and bond length. A re-evaluation of the aromaticity  of some heterocyclic molecules.W
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  208303. GABRIEL WEATHERHEAD
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  208305. Box, V. G. S.B
  208306. HeterocyclesCWFUNCTIONAL GROUPS /TRANSFORMATIONS /CARBOHYDRATES /PHYSICAL ORGANIC  /STEREOELECTRONICSM
  208307. 16284N
  208308. 2/28/96V
  208309. The role of lone pair interactions in the chemistry of the monosaccharides. Stereo-electronic  effects in unsaturated monosaccharides.W
  208310. 1991Y
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  208312. GABRIEL WEATHERHEAD
  208313. 15276
  208314. Box, V. G. S.B
  208315. HeterocyclesM
  208316. 16285N
  208317. 2/28/96V`The role of lone pair interactions in the chemistry of the monosaccharides. The anomeric effect.W
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  208325. 2/28/96V)Organometallic derivatives of fullerenes.W
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  208332. 16287N
  208333. 2/28/96VFReactivity of Substituted Aliphatic Nitro-Compounds with Nucleophiles.W
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  208340. 2/28/96VHNeighbouring group participation by carbonyl groups in ester hydrolysis.W
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  208347. 2/28/96V;Transition-metal-mediated reactions of organic isocyanates.W
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  208354. 2/28/96V#Up-scaling photochemical reactions.W
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  208360. 2/28/96V>The use of samarium diiodide in organic and p lymer synthesis.W
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  208365. 16292N
  208366. 2/28/96V^New synthesis of azaheterocycles by rearrangement of isoxazoline-5-spirocycloalkane compounds.W
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  208370. )A6Brandi, A.//Cicchi, S.//Goti, A.//Pietrusiewicz, K. M.B
  208371. Gazz. Chim. Ital.C
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  208373. 2/28/96VWRegio- and stereoselective synthesis of isoxazolidines bearing phosphinyl substituents.W
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  208388. 2/28/96V<Dynamical processes in crystalline organometallic complexes.W
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  208392. Brady, W. T.B
  208393. Tetrahedron
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  208395. 16296N
  208396. 2/28/96V5Synthetic Applications Involvi g Halogenated Ketenes.W
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  208411. 2/28/96VKThe directed synthesis of biaryl compounds: modern concepts and strategies.W
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  208427. 2/28/96V(The Intramolecular Diels-Ald r Reaction.W
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  208434. 2/28/96V!Catalytic Transfer Hydrogenation.W
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  208441. 2/28/96V9Carbon-Carbon Alkylations with Amines and Ammonium Salts.W
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  208449. 3VIOptically active amino acid synthesis by artificial transaminase enzymes.W
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  208455. 16304N
  208456. 2/28/96V&3-Alkoxyacrolein in Organic Synthesis.W
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  208458. GABRIEL WEATHERHEAD
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  208460. Bravo, P.//Resnati, G.B
  208461. Tetrahedron: AsymmetryC
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  208463. 2/28/96V=Preparation and properties of chiral fluoroorganic compounds.W
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  208465. GABRIEL WEATHERHEAD
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  208470. 2/28/96V'Reductions by Lithium Aluminum Hydride.W
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  208511. GABRIEL WEATHERHEAD
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  208526. 2/28/96V%From silylcarbinols to silaethylenes.W
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  208562. 2/28/96V!Asymmetric Homogeneous Catalysis.W
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  208593. 2/28/96V]Development of a Simple Procedure for Synthesis of Pure Enantiomers via Chiral Organoboranes.W
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  208622. 2/28/96V"Forty Years of Hydride Reductions.W
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  208624. GABRIEL WEATHERHEAD
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  208629. 2/28/96V+Explorations in The Non-classical Ion Area.W
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  208635. 2/28/96V
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  208855. 2/28/96V>Synthesis of oligosaccharides related to bacterial O-antigens.W
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  208876. 2/28/96V
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  208884. 2/28/96V5The Torsion Angle Concept in Conformational Analysis.W
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  208886. GABRIEL WEATHERHEAD
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  208892. 2/28/96V7Zirconocene compleses of unsaturated organic molecules.W
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  208907. 2/28/96V
  208908. Bredt's Rule.W
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  208910. GABRIEL WEATHERHEAD
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  208915. 2/28/96V:Thiadiazines with adjacent sulfur and nitrogen ring atoms.W
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  208917. GABRIEL WEATHERHEAD
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  208923. 2/28/96V\Synthesis of Substituted Ferrocenes and Other  -Cyclopentadienyl-Transition Metal Compounds.W
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  208925. GABRIEL WEATHERHEAD
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  208928. TetrahedronC
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  208930. 2/28/96V|Fluorinated orga ometallics: perfluoroalkyl and functionalized perfluoroalkyl organometallic reagents in organic  synthesis.W
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  208945. uVNCatalytic conversion of paraffinic hydrocarbons into isoparaffins and olefins.W
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  208947. GABRIEL WEATHERHEAD
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  208967. 2/28/96V4Intramolecular Reactions of Diazocarbonyl Compounds.W
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  208969. GABRIEL WEATHERHEAD
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  208976. GABRIEL WEATHERHEAD
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  208981. 2/28/96V/Asymmetric Syntheses Of 2,3-Methanoamino Acids.W
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  208984. GABRIEL WEATHERHEAD
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  208989. 2/28/96VESynthetic approaches to stereoisomers and analogs of castanospermine.W
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  208997. 2/28/96VaNADH mimics for the stereos lective reduction of benzoylformates to the corresponding mandelates.W
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  209013. ~V,Buckminsterfullerene. Great balls of carbon.W
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  209020. 2/28/96V+Some  ovel concepts in aromatic reactivity.W
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  209042. 2/28/96V8A New Series of Nitrene-Induced Aromatic Rearrangements.W
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  209049. 2/28/96V?Catalysis by metal ions in reactions of crown ether substrates.W
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  209102. 2/28/96VpSubstituted 1,2,3-triazolium-1-ylides as 1,3-dipoles: synthons for a range of azimine and  1,2,3-triaza systems.W
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  209126. 2/28/96VFThe Electronic Structure and Stereochemistry of Simple Carbonium Ions.W
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  209163. 2/28/96V%Homogeneous Asymmetric Hydrogenation.W
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  209311. GABRIEL WEATHERHEAD
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  209317. 2/28/96V\Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates.W
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  209339. 2/28/96V!Tin (IV) Acetylides. An Overview.W
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  209399. GABRIEL WEATHERHEAD
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  209420. 2/28/96V~Synthesis of Carboxylic Acids and Esters by Carbonylation Reactions at Atmospheric Pressure  Using Transition Metal Catalysts.W
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  209427. 2/28/96V(Synthesis of Benzoquinones by Oxidation.W
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  209495. 2/28/96V~Recent developments in the synthesis of aldehydes by reduction of carboxylic acids and their  derivatives with metal hydrides.W
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  209626. 2/28/96VLAnnulated 1,5-benzodiazepines. Part I. Three, four, and five membered rings.W
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  209645. GABRIEL WEATHERHEAD
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  209665. 2/28/96VFStructures of the Intermediate Complexes in Friedel-Crafts Acylations.W
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  209679. 2/28/96V(The Friedlander Synthesis of Quinolines.W
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  209703. 2/28/96V$Meldrum's acid in organic synthesis.W
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  209717. 2/28/96VAMolecular Rearrangements in Lithium Aluminium Hydride Reductions.W
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  209724. 2/28/96VbChiral ligands based on the pyridine framework: synthesis and application in asymmetric catalysis.W
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  209741. 2/28/96V(The Intramolecular Diels-Alder Reaction.W
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  209809. 2/28/96V6Group VIII metal-catalysed C-C bond forming sequences.W
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  209916. 2/28/96VXThe role of the alpha-effect in thermolysis, photolysis and electron-transfer processes.W
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  209955. 2/28/96VKSynthesis of therapeutically useful prostaglandin and prostacyclin analogs.W
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  209987. 2/28/96V?Recent Stereoselective Synthetic Approaches To Beta-Amino AcidsW
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  210557. KABDarensbourg, M. Y.//Ash, C. E.//Kao, S. C.//Silva, R.//Springs, J.B
  210558. Pure Appl. Chem.C
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  210561. 2/28/96VMMechanisms of group transfer in anionic transition metal hydrides and alkyls.W
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  210563. GABRIEL WEATHERHEAD
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  210565. LA Darbaruov, M.//Sundaramurthy, V.B    SynthesisCGC-C BOND FORMATION /AROMATICS /RING FORMATION /HETRING /6(O) /COUMARINS
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  210567. 2/28/96VTSynthesis of Coumarins with 3:4-Fused Ring Systems and Their Physiological Activity.W
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  210569. GABRIEL WEATHERHEAD
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  210571. Danishevsky, S. J.B
  210572. Aldrichimica ActaC
  210573. C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC /DIASTEREOGENIC /PERICYCLIC REACTIONS  /CYCLOADDITIONS /[4+2] /TARGET SYNTHESIS /STEREOCHEMISTRY /C=C-C X)=C /O-Si /DANISHEVSKY DIENE /ALDOL /DIHYDROPYRONE HETRING /6(O)M
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  210575. 2/28/96V
  210576. Reflections on Organic Synthesis: The Evolution of a General Strategy for the Stereoselective  Construction of Polyoxygenated Natural Products.W
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  210578. GABRIEL WEATHERHEAD
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  210580. Danishevsky, S.B
  210581. Acc. Chem. Res.C
  210582. C-C BOND FORMATION /PERICYCLIC REA TIONS /CYCLOADDITIONS /[4+2] /SILOXY DIENES ALDEHYDES C=C-X-M /O-Si /DANISHEVSKY DIENE  /TETRAHYDROPYRAN-4-ONES /HETRING /6(O) /SiM
  210583. 16586N
  210584. 2/28/96V!Siloxy Dienes in Total Synthesis.W
  210585. 1981X
  210586. GABRIEL WEATHERHEAD
  210587. 15578
  210588. Danishevsky, S.B
  210589. Acc. Chem. Res.
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  210591. 16587N
  210592. 2/28/96V1Electrophilic Cyclopropanes in Organic Synthesis.W
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  210594. GABRIEL WEATHERHEAD
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  210597. Chemtracts: Organic ChemistryM
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  210599. 2/28/96VqCycloadd tion and cyclocondensation reactions of highly functionalized dienes: Applications to organic synthesis.W
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  210601. GABRIEL WEATHERHEAD
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  210604. J. Fluorine Chem.M
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  210606. 2/28/96VOFluorinated peniciilins and other 
  210607. -lactams: chemistry and biological activity.W
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  210610. GABRIEL WEATHERHEAD
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  210612. Davies, S. G.B
  210613. Pure Appl. Chem.CcORGANOMETALLICS /IRON /C-C B ND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /CHIRAL AUXILIARY /FeM
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  210615. 2/28/96VNAsymmetric synthesis via the iron chiral auxiliary [(eta-5-C5H5)Fe(CO)(PPh3)].W
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  210617. GABRIEL WEATHERHEAD
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  210619. Davies, H. G.//Green, R. H.B
  210620. Nat. Prod. Rep.
  210621. SCDTARGET SYNTHESIS /MACROLIDES /SPIROACETALS /AVERMECTINS /MILBEMYCINSM
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  210624. Avermectins and Milbemycins.W
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  210629. TetrahedronC+ORGANOMETALLICS /GENERAL /C-M /ADDITION /TMM
  210630. 16592N
  210631. 2/28/96V
  210632. Nucleophilic Additions to Organotransition Metal Cations Containing Unsaturated Hydrocarbon  Ligands. A Survey and Interpretation.W
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  210638. Adv. Phys. Org. Chem.CRFUNCTIONAL GROUPS /TRANSFORMATIONS /PHOTOCHEMICAL REACTIONS /PHOTOCHEMISTRY  /Ar-XM
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  210640. 2/28/96V5Photochemistry of Aryl Halides and Related Compound .W
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  210642. GABRIEL WEATHERHEAD
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  210647. 2/28/96VDUse of Transition Organometallic Compounds in Heterocyclic SynthesisW
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  210649. GABRIEL WEATHERHEAD
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  210651. Davidson, I. M.B
  210652. Quarterly ReviewsC
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  210655. 2/28/96V*Some Aspects of Silicon Radical Chemistry.W
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  210657. GABRIEL WEATHERHEAD
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  210672. GABRIEL WEATHERHEAD
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  210677. 2/28/96VIRegiose ective Manipulation of Hydroxyl Groups via Organotin Derivatives.W
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  210679. GABRIEL WEATHERHEAD
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  210685. 2/28/96V^The Reaction of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic and Aromatic Compounds.W
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  210690. Acc. Chem. Res.CYC-C BOND FORMATION /APPENDAGES /COUPLING /ORGANOMETALLICS /E EMENT /PALLADIUM /GLYCAL /PdM
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  210692. 2/28/96VNC-glycoside synthesis by palladium-mediated glycal-aglycon coupling reactions.W
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  210697. Chem. Rev.C^C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /PALLADIUM /C=C-X /O,S,N,Si,P /C-M  /Pd /S /Si /PM
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  210699. 2/28/96VL1,2-Additions to Heteroatom-Substituted Olefins by Organopalladium Reagents.W
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  210707. 2/28/96V4New vistas in zeolite and molecular sieve catalysis.W
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  210714. 2/28/96VAAsymmetric hydroxylation of enolates with N-sulfonyloxaziridines.W
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  210716. GABRIEL WEATHERHEAD
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  210719. TetrahedronC\FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUS /C=C-X-M /O-Li /OXAZIRIDINES  /O=C(R)-C-X /(C)OHM
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  210721. 2/28/96V2Applications of Oxaziridines in Organic Synthesis.W
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  210726. aA'Davies-Coleman, M. T.//Rivett, D. E. A.M
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  210734. 2/28/96VkTandem cyclopropanation/Cope rearrangement: a general method for the construction of  seven-membered rings.W
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  210737. GABRIEL WEATHERHEAD
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  210765. 2/28/96V%Avermectins and Milbemycins. Part II.W
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  210767. GABRIEL WEATHERHEAD
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  210772. 2/28/96VBThe chiral auxiliary [C6H5)Fe(CO)(PPh3)] for asymmetric synthesis.W
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  210777. Adv. Organomet. Chem.C
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  210779. 2/28/96VCChemistry of the cyclopentadienyl bisphosphine ruthenium auxiliary.W
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  210784. Angew. Chem., Int. Ed. Engl.CXPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULES /CARBRING /3  /CYCLOPROPANEM
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  210786. 2/28/96VGThe Bonding Properties of Cyclopropane and Their Chemical Consequences.W
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  210801. 2/28/96V1Chemical relaxation methods in organic chemistry.W
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  210811. GABRIEL WEATHERHEAD
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  210813. De Lucchi, O.//Pasquato, L.B
  210814. TetrahedronCFC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /DA /SM
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  210816. 2/28/96VaThe Role of Sulphur Functionality in Activating and Directing Olefins in Cycloaddition Reactions.W
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  210819. GABRIEL WEATHERHEAD
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  210822. TetrahedronC
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  210825. 2/28/96V1Acetylene Equivalents in Cycloaddition Reactions.W
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  210833. 2/28/96VyPathways in Electrophilic Aromatic Substitution. Cyclohexadienes and Related Compounds as  Intermediates in Halogenation.W
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  210852. 2/28/96V(Bioformation of optically pure epoxides.W
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  210860. 2/28/96V(Cyclic Acetals of Aldoses and Aldosides.W
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  210867. 2/28/96V2Asymmetric synthesis using N-sulfonyloxaziridines.W
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  210877. GABRIEL WEATHERHEAD
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  210880. Angew. Chem., Int. Ed. Engl.CDODDS AND ENDS /TECHNIQUES AND METHODS /PTC /PHASE TRANSFER CATALYSISM
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  210882. 2/28/96VNPhase-Transfer Catalysed Two-Phase Reactions in Preparative Organic Chemistry.W
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  210887. Acta Chem. Scand.M
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  210889. 2/28/96VARing-opening of five-membered heteroaromatic azides and nitrenes.W
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  210897. 2/28/96V0Che ical Reactions of Newly Available Pyridines.W
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  210904. 2/28/96VCComplexes of carboxylic acids with pyridines and pyridine N-oxides.W
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  210919. 2/28/96VTCyclopropenes as Reagents for Synthesis. Cycloaddition Reactions with Cyclopropenes.W
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  210926. 2/28/96V.Cleaning-up oxidations with hydrogen peroxide.W
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  210933. 2/28/96VkExpanded Ring Systems from Cyclopropenes: 1,3-Dipolar and [2+2] Additions Across the  Cyclopropenyl  -Bond.W
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  210941. 2/28/96V:Stereochemistry of Cyclopropane Cleavage by Electrophiles.W
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  210956. 2/28/96V@Fine Feathers Make Fine Birds - The Heck Reaction In Modern GarbW
  210957. 1994X    2379-2411Y
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  210959. GABRIEL WEATHERHEAD
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  210962. SynlettCiPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULES /CARBRING /3,4  /CYCLOPROPANES /CYCLOBUTANESM
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  210965. VMTailoring the Reactivity of Small Ring Building Blocks for Organic Synthesis.W
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  210981. GABRIEL WEATHERHEAD
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  210986. 2/28/96V'Sensitised Photooxygenation of Olefins.W
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  210992. 2/28/96V;The synthesis and glycosidation of N-acetylneuraminic acid.W
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  210994. GABRIEL WEATHERHEAD
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  211000. GABRIEL WEATHERHEAD
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  211004. 2/28/96VNSelective oxidation of alpha, beta-unsaturated ketones at the alpha'-position.W
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  211011. 2/28/96V%Asymmetric boron-catalyzed reactions.W
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  211013. GABRIEL WEATHERHEAD
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  211017. 16645N
  211018. 2/28/96VlHeightened selectivity in aromatic nitrations and chlorinations by the use of solid supports and  catalysts.W
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  211021. GABRIEL WEATHERHEAD
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  211027. VIMechanistic aspects of transition metal catal sed alcohol carbonylations.W
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  211033. 2/28/96V7Compounds of dicoordinate arsenic: chemical properties.W
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  211039. 2/28/96V?Recent Advances  n the Chemistry of Chlorosulphonyl Isocyanate.W
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  211041. GABRIEL WEATHERHEAD
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  211045. 2/28/96V2Synthesis of Carboxylic and Carbonic Ortho Esters.W
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  211047. GABRIEL WEATHERHEAD
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  211053. ViMechanisms of pericyclic reactions: the role of quantitative theory in the study of reaction  mechanisms.W
  211054. 1992X
  211055. GABRIEL WEATHERHEAD
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  211058. Adv. Photochem.M
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  211060. 2/28/96V0Photochemistry and photophysics of 'onium salts.W
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  211062. GABRIEL WEATHERHEAD
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  211067. 2/28/96VMThe design and synthesis of immune regulatory agents: targets and approaches.W
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  211070. GABRIEL WEATHERHEAD
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  211075. 2/28/96VCThe Pschorr Synthesis and Related Diazonium Ring Closure Reactions.W
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  211083. Hydrolysis of Acetals and Ketals. Position of Transition States Along the Reaction Coordinates, and  Stereoelectronic Effects. 1994 R. U. Lemieux Award Lecture.W
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  211085. GABRIEL WEATHERHEAD
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  211088. Pure Appl. Chem.M
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  211090. 2/28/96VXIntramolecular strategies and stereoelectronic effects. Glycosides hydrolysis revisited.W
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  211096. Pure Appl. Chem.M
  211097. 16656N
  211098. 2/28/96VoTransannular Diels-Alder reaction on macrocycles. A general s rategy for the synthesis of polycyclic compounds.W
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  211101. GABRIEL WEATHERHEAD
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  211105. 16657N
  211106. 2/28/96V$Synthetic saccharide photochemistry.W
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  211116. GABRIEL WEATHERHEAD
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  211121. 2/28/96V,Organic Syn hesis with alpha-chlorosulfides.W
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  211132. GABRIEL WEATHERHEAD
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  211141. GABRIEL WEATHERHEAD
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  211146. 2/28/96VValpha-Oxo Ketene Dithioacetals and Related Compounds: Versatile Three-Carbon Synthons.W
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  211179. 2/28/96V"Beyond C60: The higher fullerenes.W
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  211217. 2/28/96V6Cycloadditions of fluoroallene and 1,1-difluoroallene.W
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  211225. 2/28/96V^Transition-metal fluoro compounds containing carbonyl, phosphine, arsine, and stibine ligands.W
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  211322. 2/28/96V0Synthesis and Synthetic Utility of Halolactones.W
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  211337. 2/28/96V1Tricyclo[2.1.0.0 2,5]pentane and its derivatives.W
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  211359. 2/28/96V<Carbon-Carbon Bond Formation via Carbonyl-Car ene Complexes.W
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  211379. CATALYSIS /TMM
  211380. 16693N
  211381. 2/28/96VJCatalytic applications of transition-metal complexes with sulfide ligands.W
  211382. 1989X
  211383. GABRIEL WEATHERHEAD
  211384. 15685
  211385. A%Dubac, J.//Laporterie, A.//Manuel, G.B
  211386. Chem. Rev.M
  211387. 16694N
  211388. 2/28/96VOGroup 14 metalloles. 1. Synthesis, organic chemistry, and physicochemical data.W
  211389. 1990X
  211390. GABRIEL WEATHERHEAD
  211391. 15686
  211392. Dryuk, V. G.B
  211393. TetrahedronC@C-C BOND FORMATION /HETEROANNULATIONS /3-RING /EPOXIDES,OXIRANESM
  211394. 16695N
  211395. 2/28/96V(The Mechanism of Epoxidation of Olefins.W
  211396. 1976X
  211397. 2855Y
  211398. GABRIEL WEATHERHEAD
  211399. 15687
  211400. Druliner, J. D.//Stevens, W. R.B
  211401. Adv. Catal.C
  211402. ORGANOMETALLICS /GENERAL /C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /C=C  /ALKENES /HYDROCYANATION /HOMOGENOUS NICKEL CATALYSED /R-CN /NITRILES /NiM
  211403. 16696N
  211404. 2/28/96V2Homogenous Nickel Catalysed Olefin Hydrocyanation.W
  211405. 1985X
  211406. GABRIEL WEATHERHEAD
  211407. 15688
  211408. AfDrueckhammer, D. G.//Hennen, W. J.//L., P.//Bar as, C. F. I.//Gautheron, C. M.//Krach, T.//Wong, C.-H.B    SynthesisC4FUNCTIONAL GROUPS /BIOTRANSFORMATIONS /CARBOHYDRATESM
  211409. 16697N
  211410. 2/28/96V5Enzyme catalysis in synthetic carbohydrate chemistry.W
  211411. 1991X
  211412. GABRIEL WEATHERHEAD
  211413. 15689
  211414. Drewes, S. E.//Ross, G. H. P.B
  211415. TetrahedronC
  211416. C-C BOND FORMATION /APPENDAGES /ENOLATES /1,4-ADDITION /SYNTHONS /O=C(OR)-C=C  /O=C-H /O=C-C=C /ALDEHYDE /CONJUGATE ADDITION /BUTENOLIDE LACTONE /5 O=C(R)-C-X /H,OHM
  211417. 16698N
  211418. 2/28/96VkSynthetic Potential of the Tertiary-Amine-Catalysed Reaction of Activated Vinyl Carbanions with  Aldehydes.W
  211419. 1988X
  211420. 4653Y
  211421. GABRIEL WEATHERHEAD
  211422. 15690
  211423. Drake, N. L.B
  211424. Org. React. (N.Y.)M
  211425. 16699N
  211426. 2/28/96V
  211427. The Bucherer Reaction.W
  211428. 1 42X
  211429. GABRIEL WEATHERHEAD
  211430. 15691
  211431. A*Drabowicz, J.//Kielbasinski, P.//Lyzwa, P.B
  211432. Sulfur ReportsC
  211433. 16700N
  211434. 2/28/96VMStereoselective reactions at the alpha-carbon atom in organosulfur compounds.W
  211435. 1992X
  211436. 213-96Y
  211437. GABRIEL WEATHERHEAD
  211438. 15692
  211439. Doyle, M. P.B
  211440. Recl. Trav. Chim. Pays-BasM
  211441. 16701N
  211442. 2/28/96VKChiral catalysts for enantioselective carbenoid cyclopropanation reactions.W
  211443. 1991X
  211444. GABRIEL WEATHERHEAD
  211445. 15693
  211446. Eberson, L.//Nyberg, K.B
  211447. TetrahedronC6ELECTROCHEMISTRY /ELECTROCHEMICAL /ANODIC SUBSTITUTIONM
  211448. 16702N
  211449. 2/28/96V0Synthetic Uses of Anodic Substitution Reactions.W
  211450. 1976X
  211451. 2185Y
  211452. GABRIEL WEATHERHEAD
  211453. 15694
  211454. Eaton, P. E.B
  211455. Angew. Chem., Int. Ed. Engl.M
  211456. 16703N
  211457. 2/28/96VOCubanes: starting materials for the chemist y of the 1990s and the new century.W
  211458. 1992X
  211459. 1421Y
  211460. GABRIEL WEATHERHEAD
  211461. 15695
  211462. Eaton, P. E., Ed.B
  211463. Tetrahedron Symposium-in-PrintC$TARGET SYNTHESIS /UNNATURAL PRODUCTSM
  211464. 16704N
  211465. 2/28/96V8Synthesis of Non-Natural Products: Challenge and Reward.W
  211466. 1986X
  211467. 1549Y
  211468. GABRIEL WEATHERHEAD
  211469. 15696
  211470. E., Smalley  R.B
  211471. Acc. Chem. Res.M
  211472. 16705N
  211473. 2/28/96V Self-Assembly of the fullerenes.W
  211474. 1992X
  211475. GABRIEL WEATHERHEAD
  211476. 15697
  211477. ACDuthaler, R. O.//Hafner, A.//Alsters, P. L.//Rothe, S. P.//Rihs, G.B
  211478. Pure Appl. Chem.C
  211479. Ti /Zr /HfM
  211480. 16706N
  211481. 2/28/96VtStereoselective transformations mediated by chiral monocyclopentadienyl titanium, zirconium, and  hafnium complexes.W
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  211483. 1897Y
  211484. GABRIEL WEATHERHEAD
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  211486. Duthaler, R. O.//Hafner, A.B
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  211489. 2/28/96V[Chiral titanium complexes for enantioselective addition of nucleophiles to carbonyl groups.W
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  211491. GABRIEL WEATHERHEAD
  211492. 15699
  211493. A)Duthaler, R. O.//Hafner, A.//Riediker, M.B
  211494. Pure Appl. Chem.
  211495. CxORGANOMETALLICS /TITANIUM /C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS  /CHIRAL AUXILIARY /CHIRAL CATALYST /TM
  211496. 16708N
  211497. 2/28/96VMAsymmetric carbon-carbon bond formation with titanium carbohydrate complexes.W
  211498. 1990X
  211499. GABRIEL WEATHERHEAD
  211500. 15700
  211501. Duthaler, R. O.B
  211502. TetrahedronM
  211503. 16709N
  211504. 2/28/96VJRecent developments in the stereoselective synthesis of alpha-amino acids.W
  211505. 1 94X
  211506. 1539-650Y
  211507. GABRIEL WEATHERHEAD
  211508. 15701
  211509. Durucasu, I.B
  211510. HeterocyclesM
  211511. 16710N
  211512. 2/28/96VWThe chemistry of DDATHF (5,10-dideaza-5,6,7,8-tetrahydrofolic acid) as antitumor agent.W
  211513. 1993X
  211514. 1527-49Y
  211515. GABRIEL WEATHERHEAD
  211516. 15702
  211517. Eisch, J. J.//Sexsmith, S. R.B"Research on Chemical Intermedia esC
  211518. ORGANOMETALLICS /NICKEL /NiM
  211519. 16711N
  211520. 2/28/96ViIntermediates and reaction mechanisms in the interaction of nickel(0) complexes with organic  substrates.W
  211521. 1990X
  211522. GABRIEL WEATHERHEAD
  211523. 15703
  211524. A&Einhorn, C.//Einhorn, J.//Luche, J. L.B    Synthesis
  211525. 16712N
  211526. 2/28/96VISonochemistry-the use of ultrasonic waves in synthetic organic chemistry.W
  211527. 1989X
  211528. GABRIEL WEATHERHEAD
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  211530. Eicher, T.//Weber, J. L.B
  211531. Top. Curr. Chem.CXFUNCTIONAL GROUPS /TRANSFORMATIONS /CYCLOPROPANE CLEAVAGE /CARBRING /3  /CYCLOPROPANONESM
  211532. 16713N
  211533. 2/28/96V=Structure and Reactivity of Cyclopropanones and Triaful enes.W
  211534. 1975X
  211535. GABRIEL WEATHERHEAD
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  211537. A)Eguchi, S.//Matsushita, Y.//Yamashita, K.B
  211538. Org. Prep. Proced. Int.M
  211539. 16714N
  211540. 2/28/96V2The Aza-Wittig reaction in heterocyclic synthesis.W
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  211542. GABRIEL WEATHERHEAD
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  211544. Efratz, A.B
  211545. Chem. Rev.C
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  211547. 16715N
  211548. 2/28/96V
  211549. Cyclobutadienemetal Complexes.W
  211550. 1977X
  211551. GABRIEL WEATHERHEAD
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  211553. Effenberger, F.B
  211554. Angew. Chem., Int. Ed. Engl.M
  211555. 16716N
  211556. 2/28/96V8Synthesis And Reactions Of Optic lly-Active CyanohydrinsW
  211557. 1994X    1555-1564Y
  211558. 15-16a
  211559. GABRIEL WEATHERHEAD
  211560. 15708
  211561. Effenberger, F.//Wolf, H. C.B
  211562. New Journal of ChemistryM
  211563. 16717N
  211564. 2/28/96VUTerminally substituted conjugated polyenes: synthesis and energy transfer properties.W
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  211566. GABRIEL WEATHERHEAD
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  211568. Effenberger, F.B
  211569. Angew. Chem., Int. Ed. Engl.COFUNCTIONAL GROUPS /PREPARATIONS /HETEROALKENES /C=C-X /O /ENOL ETHERS /C=C-X /OM
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  211571. 2/28/96V
  211572. The Chemistry of Enol Ethers.W
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  211574. GABRIEL WEATHERHEAD
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  211576. Effenberger, F.M
  211577. 16719N
  211578. 2/28/96a
  211579. GABRIEL WEATHERHEAD
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  211582. J. Heterocycl. Chem.M
  211583. 16720N
  211584. 2/28/96V+Polysulfur-nitrogen heterocyclic chemistry.W
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  211587. GABRIEL WEATHERHEAD
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  211591. 16721N
  211592. 2/28/96V(Arsenic compounds from marine organisms.W
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  211595. GABRIEL WEATHERHEAD
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  211597. A    echer, J.B    SynthesisCTFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /GLUTACONALDEHYDE  /AMINOPENTADIENALS
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  211599. 2/28/96VISynthesis and Reactions of Glutaconaldehyde and 5-Amino-2,4-pentadienals.W
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  211601. GABRIEL WEATHERHEAD
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  211603. ACEbetino, F. H.//Degenhardt, C. R.//Jamieson, L. A.//Brudsall, D. C.B
  211604. HeterocyclesM
  211605. 16723N
  211606. 2/28/96VQRecent work on the synthesis of phosphonate-containing, bone-active heterocycles.W
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  211608. GABRIEL WEATHERHEAD
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  211610. Ellis, J. E.B
  211611. Adv. Organomet. Chem.M
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  211613. 2/28/96V[Highly reduced metal carbonyl anions: synthesis, characterization, and chemical properties.W
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  211615. GABRIEL WEATHERHEAD
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  211619. 16725N
  211620. 2/28/96V
  211621. Cyanation of Aromatic Halides.W
  211622. 1987X
  211623. GABRIEL WEATHERHEAD
  211624. 15717
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  211626. Contemporary Organic Synthesis M
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  211628. 2/28/96V;Recent Developments in the Synthesis of Medium-Ring Ethers.W
  211629. 1994X
  211630. 457-474Y
  211631. GABRIEL WEATHERHEAD
  211632. 15718
  211633. Eller, K.//Schwarz, H.B
  211634. Chem. Rev.C*ORGANOMETALLICS /GENERAL /PHYSICAL ORGANICM
  211635. 16727N
  211636. 2/28/96V*Organometallic chemistry in the gas phase.W
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  211639. GABRIEL WEATHERHEAD
  211640. 15719
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  211642. Top. Curr. Chem.C!PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  211644. 2/28/96V$Protostereoisomerism (Prochirality).W
  211645. 1982X
  211646. GABRIEL WEATHERHEAD
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  211648. Eliel, E. L.B
  211649. Angew. Chem., Int. Ed. Engl.C!PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  211651. 2/28/96VQConformational Analysis in Heterocyclic Systems: Recent Results and Applications.W
  211652. 1972X
  211653. GABRIEL WEATHERHEAD
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  211656. Acc. Chem. Res.C/PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATIONM
  211657. 16730N
  211658. 2/28/96V<Conformational Analysis in Saturated Heterocycli  Compounds.W
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  211660. GABRIEL WEATHERHEAD
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  211664. 2/28/96a
  211665. GABRIEL WEATHERHEAD
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  211667. A!El-Rayyes, N. R.//Al-Awadi, N. A.B    SynthesisChC-C BOND FORMATION /HETEROANNULATIONS /5-RING /1,3-DIPOLAR CYCLOADDI ION /PYRAZOLINES,PYRAZOLIDINEDIONESM
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  211669. 2/28/96V6Synthesis of 2-Pyrazolines and 3,5-Pyrazolidinediones.W
  211670. 1985X
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  211672. GABRIEL WEATHERHEAD
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  211677. 2/28/96V`Condensed 1,2,4-triazines: I. Fused to heterocycles with three-, four-, and five-membered rings.W
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  211679. GABRIEL WEATHERHEAD
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  211685. 2,3,4-Furantriones.W
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  211692. 2/28/96V6Transition-state modeling with empirical force fields.W
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  211698. Pure Appl. Chem.C
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  211701. Di-pi-methane-like photorearrangements of alpha, beta-unsaturated organoboranes in the  synthesis of borirenes and boracarbenoid intermedi tes.W
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  211703. GABRIEL WEATHERHEAD
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  211709. 2/28/96V"Phosphorus Addition at sp2 Carbon.W
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  211711. GABRIEL WEATHERHEAD
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  211713. Endo, A.//Hasumi, K.B
  211714. Nat. Prod. Rep.M
  211715. 16738N
  211716. 2/28/96V
  211717. HMG-CoA reductase inhibitors.W
  211718. 1993X
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  211720. GABRIEL WEATHERHEAD
  211721. 15730
  211722. Emerson, W. S.B
  211723. Org. React. (N.Y.)M
  211724. 16739N
  211725. 2/28/96V2The Preparation of Amines by Reductive Alkylation.W
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  211727. GABRIEL WEATHERHEAD
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  211729. Emde, H.//Dornsch, D.//Feger, H.//Frick, U.//Gotz, A.//Hergott, H. H.//Hofmann, K.//Kober, W.//Krogelsch, K.//Oesterle, T.//Stepp, W.B    SynthesisCyFUNC IONAL GROUPS /PROTECTION /HYDROXYL /CF3SO2X /OSi /SILYL TRIFLATES /SILYL  TRIFLUOROMETHANESULFONATES /PROTECTION /SiM
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  211731. 2/28/96
  211732. VpTrialkylsilylperfluoroalkanesulfonates: Highly Reactive Silylating Agents and Lewis Acids in  Organic Synthesis.W
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  211734. GABRIEL WEATHERHEAD
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  211736. A1Elsevier, C. J.//Muller, F.//Vrieze, K.//Zoet, R.B
  211737. New Journal of ChemistryM
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  211740. Site selectivity and crucial intermediates in the reactions of homo- and hetero-bimetallic  compounds ....with molecular hydrogen and alkynes.W
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  211742. GABRIEL WEATHERHEAD
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  211745. SynlettM
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  211747. 2/28/96VqAlkylheteroaromatics as building blocks for the synthesis of condensed polyfunctionally substitut d heterocycles.W
  211748. 1994X
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  211750. GABRIEL WEATHERHEAD
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  211753. Adv. Heterocycl. Chem.M
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  211755. 2/28/96VPChemistry of pyrazoles condensed to heteroaromatic five- and six-membered rings.W
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  211757. GABRIEL WEATHERHEAD
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  211759. A-Elnagdi, M. H.//Shoig, S. M.//Mohareeb, R. M.
  211760. Heterocycles
  211761. C-C BOND FORMATION /HETEROANNULATIONS /5-RING /6-RING /C-X /CN /NITRILES /FURANS  /THIOPHENES /PYRROLE /1,2-OXAZOLE /1,3-OXAZOLES /1,2-TH AZOLES /1,3-THIAZOLES /PYRAZOLES /IMIDAZOLES /TRIAZOLES /PYRANS /COUMARINS  /THIOPYRANS /PYRIDINES /QUINOLINES /PYRIDAZINE
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  211763. 2/28/96VCThe Synthetic Potentialities of Nitriles in Heterocyclic Synthesis.W
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  211765. GABRIEL WEATHERHEAD
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  211767. Ellison, R. A.B    SynthesisC=C-C BOND FORMATION /ANNULATIONS /5-RING /2-CYCLOPENTEN-1-ONESM
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  211769. 2/28/96V0Methods for the Synthesis of 3-Oxocyclopentenes.W
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  211771. GABRIEL WEATHERHEAD
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  211774. 16746N
  211775. 2/28/96VJCycloaddition of nitrile oxides to multiple bonds containing a heteroat m.W
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  211783. 2/28/96V8Chemistry of potentially prebiological natural products.
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  211791. Synthesis of Prostaglandins.W
  211792. 1976X
  211793. GABRIEL WEATHERHEAD
  211794. 15740
  211795. A    Erker, G.B
  211796. Pure Appl. Chem.C
  211797. 16749N
  211798. 2/28/96V3Stereoselective synthesis with zirconium complexe .W
  211799. 1992X
  211800. GABRIEL WEATHERHEAD
  211801. 15741
  211802. A    Erker, G.B
  211803. Pure Appl. Chem.C
  211804. ORGANOMETALLICS /ZIRCONIUM /ZrM
  211805. 16750N
  211806. 2/28/96V7Stereochemistry and catalysis with zirconium complexes.W
  211807. 1991X
  211808. GABRIEL WEATHERHEAD
  211809. 15742
  211810. A6Erker, G.//Aulbach, M.//Mena, M.//Pfaff, R.//Sosna, F.B
  211811. Chem. Scr.C
  211812. ORGANOMETALLICS /ZIRCONIUM /ZrM
  211813. 16751N
  211814. 2/28/96VOCarbon-carbon bond formation by means of zirconocene-derived carbene complexes.W
  211815. 1989X
  211816. GABRIEL WEATHERHEAD
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  211818. A    Erker, G.B
  211819. Angew. Chem., Int. Ed. Engl.
  211820. CtORGANOMETALLICS /TITANIUM /ZIRCONIUM /HAFNIUM /CARBENOIDS /C-M /Ti /C-M /Zr /C-M  /Hf /METALLOCENE CARBENE  OMPLEXESM
  211821. 16752N
  211822. 2/28/96VXMetallocene Carbene Complexes and Related Compounds of Titanium, Zirconium, and Hafnium.W
  211823. 1989X
  211824. GABRIEL WEATHERHEAD
  211825. 15744
  211826. A    Erker, G.B
  211827. Acc. Chem. Res.C-ORGANOMETALLICS /ZIRCONIUM /CARBONYLATION /ZrM
  211828. 16753N
  211829. 2/28/96V'Carbonylation of Zirconocene Complexes.W
  211830. 1984X
  211831. GABRIEL WEATHERHEAD
  211832. 15745
  211833. Erian, A. W.B
  211834. Chem. Rev.M
  211835. 16754N
  211836. 2/28/96VSThe chemistry of 
  211837. -enaminonitriles as versatile reagents in  eterocyclic synthesis.W
  211838. 1993X    1991-2005Y
  211839. GABRIEL WEATHERHEAD
  211840. 15746
  211841. A    Erdik, E.B
  211842. TetrahedronM
  211843. 16755N
  211844. 2/28/96V<Transition metal catalyzed reactions of organozinc reagents.W
  211845. 1992X
  211846. 9577Y
  211847. GABRIEL WEATHERHEAD
  211848. 15747
  211849. Erdik, E.//Ay, M.B
  211850. Chem. Rev.M
  211851. 16756N
  211852. 2/28/96V&Electrophilic amination of carbanions.W
  211853. 1989X
  211854. 1947Y
  211855. GABRIEL WEATHERHEAD
  211856. 15748
  211857. A    Erdik, E.
  211858. TetrahedronC
  211859. ORGANOMETALLICS /ZINC /ZnM
  211860. 16757N
  211861. 2/28/96V2Use of Activation Methods for Organozinc Reagents.W
  211862. 1987X
  211863. 2203Y
  211864. GABRIEL WEATHERHEAD
  211865. 15749
  211866. A    Erdik, E.B
  211867. TetrahedronC#ORGANOMETALLICS /COPPER /Cu /Li /MgM
  211868. 16758N
  211869. 2/28/96VFCopper(I)-Catalysed Reactions of Organolithiums and Grignard Reagents.W
  211870. 1984X
  211871. GABRIEL WEATHERHEAD
  211872. 15750
  211873. erber, R. C.B
  211874. J. Organomet. Chem.CjPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBANIONS /STEREOELECTRONICS  /ORGANOMETALLICS /GENERAL /Fe /CrM
  211875. 16759N
  211876. 2/28/96VWInteraction of organometallic moieties with carbanions and other electron rich centers.W
  211877. 1983X
  211878. GABRIEL WEATHERHEAD
  211879. 15751
  211880. Ephritikhine, M.B
  211881. New Journal of ChemistryC
  211882. 16760N
  211883. 2/28/96V,Recent advanc s in organoactinide chemistry.W
  211884. 1992X
  211885. 451-69Y
  211886. GABRIEL WEATHERHEAD
  211887. 15752
  211888. Engman, L.B
  211889. Acc. Chem. Res.C#ORGANOMETALLICS /TELLURIUM /C-M /TeM
  211890. 16761N
  211891. 2/28/96V4Synthetic Applications of Organotellurium Chemistry.
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  211893. GABRIEL WEATHERHEAD
  211894. 15753
  211895. Engels, J. W.//Uhlmann, E.B
  211896. Angew. Chem., Int. Ed. Engl.C
  211897. BIOCHEMISTRY /GENESM
  211898. 16762N
  211899. 2/28/96V
  211900. Gene synthesis.W
  211901. 1989X
  211902. GABRIEL WEATHERHEAD
  211903. 15754
  211904. Fahey, R. C.B
  211905. Top. Stereochem.CmPHYSICA  ORGANIC /STEREOCHEMISTRY /MECHANISMS /OLEFINS /ACETYLENES /ALKENES /ALKYNES  /ELECTROPHILIC ADDITIONM
  211906. 16763N
  211907. 2/28/96VIThe Stereochemistry of Electrophilic Additions to Olefins and Acetylenes.W
  211908. 1968X
  211909. GABRIEL WEATHERHEAD
  211910. 15755
  211911. A*Fagan, P. J.//Calabrese, J. C.//Malone, B.B
  211912. Acc. Chem. Res.M
  211913. 16764N
  211914. 2/28/96V.Metal complexes of buckminsterfullerene (C60).W
  211915. 1992X
  211916. GABRIEL WEATHERHEAD
  211917. 15756
  211918. Faber, K.//Riva, S.B    SynthesisM
  211919. 16765N
  211920. 2/28/96V,Enzyme-catalyzed irreversible acyl transfer.W
  211921. 1992X
  211922. GABRIEL WEATHERHEAD
  211923. 15757
  211924. F rstner, A.B    Synthesis
  211925. C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /ENOLATES /ORGANOMETALLICS /ZINC  /O=C(R)-C-X /(O)Br /ANNULATION /6-RING ANNULATION /7-RING /REFORMATSKY /LACTONES  /5,6 /O=C(R)-C-C-X /(O)OHM
  211926. 16766N
  211927. 2/28/96V,Recent Advances in the Reformatsky Reaction.W
  211928. 1989X
  211929. GABRIEL WEATHERHEAD
  211930. 15758
  211931. Evans, P. A.//Holmes, A. B.B
  211932. TetrahedronCKC-C BOND FORMATION /HETEROANNULATIONS /MEDIUM RING /HETRING /7(N),8(N),9 N)M
  211933. 16767N
  211934. 2/28/96V"Medium ring nitrogen heterocycles.W
  211935. 1991X
  211936. 9131Y
  211937. GABRIEL WEATHERHEAD
  211938. 15759
  211939. Evans, W. J.B
  211940. Adv. Organomet. Chem.C
  211941. ORGANOMETALLICS /LANTHANIDESM
  211942. 16768N
  211943. 2/28/96V$Organometallic Lanthanide Chemistry.W
  211944. 1985X
  211945. GABRIEL WEATHERHEAD
  211946. 15760
  211947. Evans, W. J.B
  211948. J. Organomet. Chem.C%ORGANOMETALLICS /LANTHANIDES /C-M /LaM
  211949. 16769N
  211950. 2/28/96V.Recent advances in organolanthanide chemistry.W
  211951. 1983X
  211952. GABRIEL WEATHERHEAD
  211953. 15761
  211954. A)Evans, D. A.//Nelson, J. V.//Taber, T. R.B
  211955. Top. Stereochem.
  211956. CQC-C BOND FORMATION /APPENDAGES /1,2-ADDITION /STEREOCHEMISTRY /ALDOL CONDENSATIONM
  211957. 16770N
  211958. 2/28/96V$Stereoselective Aldol Condensations.W
  211959. 1982X
  211960. GABRIEL WEATHERHEAD
  211961. 15762
  211962. Evans, D. A.B
  211963. Aldrichimica ActaC
  211964. C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /DIASTEREOGENIC REACTIONS /ENOLATES  /ENANTIOGENIC REACTIONS /STEREOCHEMISTRY /C=C-X-M /O-B /ENOLATESM
  211965. 16771N
  211966. 2/28/96VVStudies in Asymmetric Synthesis. The Development of Practical Chiral Enolate Synthons.W
  211967. 1982X
  211968. GABRIEL WEATHERHEAD
  211969. 15763
  211970. A6Evans, D. A.//Hart, D. J.//Koelsch, P. M.//Cain, D. A.B
  211971. Pure Appl. Chem.C.C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGEM
  211972. 16772N
  211973. 2/28/96VMNew Alternatives to Oxidative Phenolic Coupli g in Natural Product Synthesis.W
  211974. 1979X
  211975. 1285Y
  211976. GABRIEL WEATHERHEAD
  211977. 15764
  211978. Evans, D. A.//Andrews, G. C.B
  211979. Acc. Chem. Res.C|C-C BOND FORMATION /APPENDAGES /ALKYLATION /SIGMATROPIC /[2,3] /SULPHUR /C=C-C-X  /SO /SULFOXIDES /C=C-C-X /OH /ALKOHOLES /SM
  211980. 16773
  211981. 2/28/96V?Allylic Sulphoxides: Useful Intermediates in Organic Synthesis.W
  211982. 1974X
  211983. GABRIEL WEATHERHEAD
  211984. 15765
  211985. A&Esser, P.//Pohlmann, B.//Scharf, H. D.B
  211986. Angew. Chem., Int. Ed. Engl.M
  211987. 16774N
  211988. 2/28/96V;The Photochemical-Synthesis Of Fine Chemicals With SunlightW
  211989. 1994X    2009-2023Y
  211990. GABRIEL WEATHERHEAD
  211991. 15766
  211992. Espenson, J. H.B
  211993. Acc. Chem. Res.C
  211994. 16775N
  211995. 2/28/96V+Chemistry of organochromium(III) complexes.W
  211996. 1992X
  211997. GABRIEL WEATHERHEAD
  211998. 15767
  211999. Esker, J. L.//Newcomb, M.B
  212000. Adv. Heterocycl. Chem.M
  212001. 16776N
  212002. 2/28/96VlThe generation of nitrogen radicals and their cyclizations for the construction of the pyrrolidine  nucleus.W
  212003. 1993X
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  212005. GABRIEL WEATHERHEAD
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  212007. AhFeringa, B. L.//De Lange, B.//Jansen, J. F. G. A.//De Jong, J. C.//Lubben, M.//Faber, W.//Schudde, E. P.M
  212008. 16777N
  212009. 2/28/96a
  212010. GABRIEL WEATHERHEAD
  212011. 15769
  212012. Felkin, H.//Swie czewski, G.B
  212013. TetrahedronC
  212014. ORGANOMETALLICS /MAGNESIUM /Mg
  212015. 16778N
  212016. 2/28/96V>Activation of Grignard Reagents by Transition Metal Compounds.W
  212017. 1975X
  212018. 2735Y
  212019. GABRIEL WEATHERHEAD
  212020. 15770
  212021. Feinauer, R.B    SynthesisCWFUNCTIONAL GROUPS /PREPARATIONS /ETHERS AND ACETALS /C-X(Y)(Z) /N(O)(O) /AMIDE  ACETALSM
  212022. 16779N
  212023. 2/28/96V0Bicyclic Amide Acetals. Synthesis and Reactions.W
  212024. 1971X
  212025. GABRIEL WEATHERHEAD
  212026. 15771
  212027. Fehr, C.//Galinder, J.B
  212028. JACSC]C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /C=C-X-M /O-Li /ENOLATES  /PROTONATIONM
  212029. 16780N
  212030. 2/28/96V<Enantioselective Protonation of Enolates Using Chiral Acids.W
  212031. 1988X
  212032. 6909Y
  212033. GABRIEL WEATHERHEAD
  212034. 15772
  212035. Fehlhammer, W. P.//Fritz, M.B
  212036. Chem. Rev.M
  212037. 16781N
  212038. 2/28/96VDEmergence of a CNH and cyano complex based organometallic chemistry.W
  212039. 1993X
  212040. 12 3-80Y
  212041. GABRIEL WEATHERHEAD
  212042. 15773
  212043. Faulkner, D. J.B    SynthesisCFFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /STEREOCHEMISTRY /C=C /TRISUBM
  212044. 16782N
  212045. 2/28/96
  212046. V4Stereoselective Synthesis of Trisubstituted Olefins.W
  212047. 1971X
  212048. GABRIEL WEATHERHEAD
  212049. 15774
  212050. Fatiadi, A.B    SynthesisCFFUNCTIONAL GROUPS /OXIDATION /ALKENES AND ALKYNES /PERMANGANATE /KMnO4M
  212051. 16783N
  212052. 2/28/96VKThe Classical Permangana e Ion /Still a Novel Oxidant in Organic Chemistry.W
  212053. 1987X
  212054. GABRIEL WEATHERHEAD
  212055. 15775
  212056. Fatiadi, A. J.B    SynthesisC
  212057. REAGENTSM
  212058. 16784N
  212059. 2/28/96VCNew Applications of Tetracyanoethylene in Organometallic Chemistry.W
  212060. 1987X
  212061. GABRIEL WEATHERHEAD
  212062. 15776
  212063. Fatiadi, A. J.B    SynthesisC;REAGENTS /NaIO4 /HIO4 /PERIODIC ACID /PERIODATES /OXIDATIONM
  212064. 16785N
  212065. 2/28/96VUNew Applications of Periodic Acid and Periodates in Organic and Bioorganic Chemistry.W
  212066. 1974X
  212067. GABRIEL WEATHERHEAD
  212068. 15777
  212069. Farina, V.//Kant, J.B
  212070. SynlettM
  212071. 16786N
  212072. 2/28/96VsThe Development Of Organometallic Methodologies For The Stereospecific  Introduction Of  Cephalosporin Side-Chains.W
  212073. 1994X
  212074. 565-574Z
  212075. GABRIEL WEATHERHEAD
  212076. 15778
  212077. A,Farcasiu, D.//Balaban, A. T.//Bologna, U. L.B
  212078. HeterocyclesM
  212079. 16787N
  212080. 2/28/96V4One-electron transfer reactions of pyrylium cations.W
  212081. 1994X
  212082. 1165-92Y
  212083. GABRIEL WEATHERHEAD
  212084. 15779
  212085. Fanta, P. E.B    SynthesisC_C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE /NAME REACTIONS /ARENES /ULLMAN  /Ar-Ar /BIARYLSM
  212086. 16788N
  212087. 2/28/96V!The Ullmann Synthesis of Biaryls.W
  212088. 1974X
  212089. GABRIEL WEATHERHEAD
  212090. 15780
  212091. Fang, J. M.//Wong, C. H.B
  212092. SynlettM
  212093. 16789N
  212094. 2/28/96V\Enzymes In Organic-Synthesis - Alteration Of Reversible-Reactions To  Irreversible-ProcessesW
  212095. 1994X
  212096. 393-402Z
  212097. GABRIEL WEATHERHEAD
  212098. 15781
  212099. Falck, P.//Monteil, F.B
  212100. Adv. Organomet. Chem.M
  212101. 16790N
  212102. 2/28/96V6Use of water-soluble ligands in homogeneous catalysis.W
  212103. 1992X
  212104. GABRIEL WEATHERHEAD
  212105. 15782
  212106. Fink, J.//Regitz, M.B    SynthesisCbFUNCTIONAL GROUPS /PREPARATIONS /HETEROCUMULENES /X=Y=Z /C,N,N /DIAZO  /ELECTROPHILIC SUBSTITUTIONM
  212107. 16791N
  212108. 2/28/96
  212109. V'Electrophilic Diazoalkane Substitution.W
  212110. 1985X
  212111. GABRIEL WEATHERHEAD
  212112. 15783
  212113. Fine , J.-P.B
  212114. Chem. Rev.CxC-C BOND FORMATION /APPENDAGES /COUPLING /AROMATICS /RING FUNCTIONALISATION /C-M  /Bi /ORGANOBISMUTH REAGENTS /ARYLATIONM
  212115. 16792N
  212116. 2/28/96V0Arylation Reactions with Organobismuth Reagents.W
  212117. 1989X
  212118. 1487Y
  212119. GABRIEL WEATHERHEAD
  212120. 15784
  212121. A*Findeisen, K.//Wagner, K.//Holtschmidt, H.B    SynthesisCvFUNCTIONAL GROUPS /TRANSFORMATIONS /C-X TO C-Y /O=C-X TO O=C-Y /C-OH /O=C-OH  /O=C-H /SUBSTITU ION /C-Cl /O=C-Cl /CCl2M
  212122. 16793N
  212123. 2/28/96V`Reaction of the Substituted 1,3,3-trichloro-2-aza-propene  [N-(1,1-dichloroalkyl)-imidchloride].W
  212124. 1972X
  212125. GABRIEL WEATHERHEAD
  212126. 15785
  212127. A5Fillol, L.//Miranda, M. A.//Morera, I. M.//Sheikh, H.B
  212128. HeterocyclesM
  212129. 16794N
  212130. 2/28/96V.Photochemistry of 2(3H)- and 2(5H)- furanones.W
  212131. 1990X
  212132. GABRIEL WEATHERHEAD
  212133. 15786
  212134. Fieser, L. F.B
  212135. Org. React. (N.Y.)M
  212136. 16795N
  212137. 2/28/96V
  212138. The Elbs Reaction.W
  212139. 1942X
  212140. GABRIEL WEATHERHEAD
  212141. 15787
  212142.  A    Field, L.B
  212143. Sulfur ReportsC
  212144. 16796N
  212145. 2/28/96V6Forty-five years with a hydra, organosulfur chemistry.W
  212146. 1993X
  212147. 197-277Y
  212148. GABRIEL WEATHERHEAD
  212149. 15788
  212150. !A    Field, L.B    SynthesisC
  212151. FUNCTIONA  GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C-X /SH /S=C-X /OH /C-X(Y) /S(S)  /X=Y=Z /N,C,S /C-X-Y /SOH /C-X /SO /C-X /SO2 /SM
  212152. 16797N
  212153. 2/28/96V?Some Recent Developments in Synthetic Organic Sulfur Chemistry.W
  212154. 1972X
  212155. GABRIEL WEATHERHEAD
  212156. 15789
  212157. Ficini, J.B
  212158. TetrahedronC:FUNCTIONAL GROUPS /PREPARATIONS /ALKYNES /YNAMINE /CC-X /NM
  212159. 16798N
  212160. 2/28/96V/Ynamine: A Versatile Tool in Organic Synthesis.W
  212161. 1976X
  212162. 1449Y
  212163. GABRIEL WEATHERHEAD
  212164. 15790
  212165. Fiandanese, V.B
  212166. Pure Appl. Chem.M
  212167. 16799N
  212168. 2/28/96VBSequential cross-coupling reactions as a versatile synthetic tool.W
  212169. 1990X
  212170. 1987Y
  212171. GABRIEL WEATHERHEAD
  212172. 15791
  212173. $A%Fetizon, M.//Goulaovic, P.//Hanna, I.B
  212174. Heterocycles
  212175. FUNCTIONAL GROUPS /PREPARATIONS /HETEROALKENES /HETEROCYCLES /PHOTOCHEMICAL  /ADDITION /O=C(R)-C-X /O /O=C(R)-C-X /O /O=C-C(X)(Y) /(S)(S) /O=C-COOHM
  212176. 16800N
  212177. 2/28/96VAThe Chemistry of 1,4-Dioxene (2,3-Dihydro-1,4-dioxin). Part VIII.W
  212178. 1989X
  212179. GABRIEL WEATHERHEAD
  212180. 15792
  212181. Ferrier, R. J.//Middleton, S.B
  212182. Chem. Rev.M
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  212184. 2/28/96V^The conversion of carbohydrate derivatives into functiona ized cyclohexanes and cyclopentanes.W
  212185. 1993X
  212186. 2779-831Y
  212187. GABRIEL WEATHERHEAD
  212188. 15793
  212189. Fleet, G. W. J.B    Chem. Br.C
  212190. CHIRONS / ARBOHYDRATES /SUGARSM
  212191. 16802N
  212192. 2/28/96V!Homochiral Compounds from Sugars.W
  212193. 1989X
  212194. GABRIEL WEATHERHEAD
  212195. 15794
  212196. Flanagan, D. M.//Joullie, M. M.B
  212197. HeterocyclesC
  212198. USEFUL FRAGMENTS /HETEROCY LES /L-MALIC ACID /L-ASPARTIC ACID /L-GLUTAMIC ACID /1,2,4-BUTANETRIOL  /1,4-DICHLORO-2-BUTENE /PYRROLIDINOLM
  212199. 16803N
  212200. 2/28/96V^Synthetic Strategies for the Construction of 3-Pyrrolidinol, a Versatile Nitrogen Heterocycle.W
  212201. 1987X
  212202. 2247Y
  212203. GABRIEL WEATHERHEAD
  212204. 15795
  212205. Fisher, L. E.//Muchowski, J. M.B
  212206. Org. Prep. Proced. Int.C6FUNCTIONAL GROUPS /PREPARATIONS /ALDEHYDES AND KETONESM
  212207. 16804N
  212208. 2/28/96VESynthesis of alpha-amino aldehydes and alpha-amino ketones. A review.W
  212209. 1990X
  212210. GABRIEL WEATHERHEAD
  212211. 15796
  212212. Fischer, G.B
  212213. Adv. Heterocycl. Chem.M
  212214. 16805N
  212215. 2/28/96V!1,2,4-Triazolo[1,5-a]pyrimidin s.W
  212216. 1993X
  212217. 82-138Y
  212218. GABRIEL WEATHERHEAD
  212219. 15797
  212220. Fischer, E.B
  212221. Sulfur ReportsC
  212222. 16806N
  212223. 2/28/96V<Synthesis, reactions and structure of 1,2,4,6-thiatriazines.W
  212224. 1992X
  212225. GABRIEL WEATHERHEAD
  212226. 15798
  212227. Fischer, R. H.//Weitz, H. M.B     ynthesisCJFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /O=C-C-X /NO2 /NITROKETONESM
  212228. 16807N
  212229. 2/28/96V7Preparation and Reactions of Cyclic alpha-Nitroketones.W
  212230. 1980X
  212231. GABRIEL WEATHERHEAD
  212232. 15799
  212233. Fischer, N. H.B    SynthesisCKFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /CHELOTROPIC /C=C /EPISULPHONES /SM
  212234. 16808N
  212235. 2/28/96
  212236. ,V8The Synthesis of Episulphones and Olefins via Sulphenes.W
  212237. 1970X
  212238. GABRIEL WEATHERHEAD
  212239. 15800
  212240. Firestone, R. A.B
  212241. TetrahedronCyPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /MECHANISMS /CYCLOADDITIONS  /[3+2] /1,3-DIPOLAR /PERICYCLIC REACTIONSM
  212242. 16809N
  212243. 2/28/96VXThe Diradical Mechanism for 1,3-Dipolar Cycloadditions and Related Pericyclic Reactions.W
  212244. 1977X
  212245. 3009Y
  212246. GABRIEL WEATHERHEAD
  212247. 15801
  212248. Ford, W. T.B
  212249. Acc. Chem. Res.C7PHYSICAL ORGANIC /MECHANISMS /ELIMINATION /C=C /ALKENESM
  212250. 16810N
  212251. 2/28/96V<Mechanisms of Elimination Reactions Catalysed by Weak Bases.W
  212252. 1973X
  212253. GABRIEL WEATHERHEAD
  212254. 15802
  212255. /A,Fokin, A. V.//yutin, V. Y.//Chkanikov, N. D.B Russ. Chem. Rev. (Engl. Transl.)C
  212256. 16811N
  212257. 2/28/96V=The chemistry of perfluoroalkyl-substituted dicyanoethylenes.W
  212258. 1992X
  212259. GABRIEL WEATHERHEAD
  212260. 15803
  212261. 0A4Fokin, A. V.//Allakhverdiev, M. A.//Kolomiets, A. F.B Russ. Chem. Rev. (Engl. Transl.)C
  212262. 16812N
  212263. 2/28/96
  212264. 0V*New advances in the chemistry of thiirans.W
  212265. 1990X
  212266. GABRIEL WEATHERHEAD
  212267. 15804
  212268. Fodor, G.//Dharanipragada, R.B
  212269. Nat. Prod. Rep.M
  212270. 16813N
  212271. 2/28/96V
  212272. Tropane alkaloids.W
  212273. 1993X
  212274. 199-206Y
  212275. GABRIEL WEATHERHEAD
  212276. 15805
  212277. Fodor, G.//Nagubandi, S.M
  212278. 16814N
  212279. 2/28/96V}Correlation of the von Braun, Ritter, Bischler-Napieralski, Beckmann, and Schmidt Reactions via  Nitrilium Salt IntermediatesW
  212280. 1980a
  212281. GABRIEL WEATHERHEAD
  212282. 15806
  212283. 3A&Fodor, G.//Fumeau, J.-P.//Sankaran, V.B    SynthesisCQC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETRING /6(N) /PYRIDINESM
  212284. 16815N
  212285. 2/28/96VNSynthesis of Carpyrinic Acid and Related Pyridines with Long Aliphatic Chains.W
  212286. 1972X
  212287. GABRIEL WEATHERHEAD
  212288. 15807
  212289. 4A&Floyd, A. J.//Dyke, S. F.//Ward, S. E.B
  212290. Chem. Rev.C<C-  BOND FORMATION /AROMATICS /RING FORMATION /PHENANTHRENESM
  212291. 16816N
  212292. 2/28/96V
  212293. Synthesis of Phenanthrenes.W
  212294. 1976X
  212295. GABRIEL WEATHERHEAD
  212296. 15808
  212297. Floss, H. G.//Lee, S.B
  212298. Acc. Chem. Res.M
  212299. 16817N
  212300. 2/28/96V)Chiral methyl groups: small is beautiful.W
  212301. 1993X
  212302. GABRIEL WEATHERHEAD
  212303. 15809
  212304. Floss, H. G.//Strohl, W. R.B
  212305. TetrahedronM
  212306. 16818N
  212307. 2/28/96V=Genetic engineering of hybrid antibiotics. A progress report.W
  212308. 1991X
  212309. 6045Y
  212310. GABRIEL WEATHERHEAD
  212311. 15810
  212312. Flood, T. C.B
  212313. Top. Stereoc em.C?PHYSICAL ORGANIC /STEREOCHEMISTRY /ORGANOMETALLICS /GENERAL /TMM
  212314. 16819N
  212315. 2/28/96VHStereochemistry of the Reactions of Transition Metal-Carbon Sigma Bonds.W
  212316. 1981X
  212317. GABRIEL WEATHERHEAD
  212318. 15811
  212319. Flitsch, W.B
  212320. Adv. Heterocycl. Chem.C
  212321. HETEROCYCLESM
  212322. 16820N
  212323. 2/28/96V
  212324. The chemistry of 4-azaazulenes.W
  212325. 1988X
  212326. GABRIEL WEATHERHEAD
  212327. 15812
  212328. Flits h, W.B
  212329. Adv. Heterocycl. Chem.C
  212330. HETEROCYCLESM
  212331. 16821N
  212332. 2/28/96V4Hydrogenated porphyrin derivatives: hydroporphyrins.W
  212333. 1988X
  212334. GABRIEL WEATHERHEAD
  212335. 15813
  212336. :A'Fleming, I.//Dunogues, J.//Smithers, R.B
  212337. Org. React. (N.Y.)
  212338. :CPORGANOMETALLICS /SILICON /C=C-M /Si /C=C-C-M /Si /ELECTROPHILIC SUBSTITUTION /SiM
  212339. 16822N
  212340. 2/28/96V@The electrophilic substitution of allylsilanes and vinylsilanes.W
  212341. 1989X
  212342. GABRIEL WEATHERHEAD
  212343. 15814
  212344. ;A?Fraser-Reid, B.//Merritt, J. R.//Handlon, A. L.//Andrews, C. W.B
  212345. Pure Appl. Chem.M
  212346. 16823N
  212347. 2/28/96V^The chemistry of N-pentenyl glycosides: synthetic, theoretical, and mechanistic ramifications.W
  212348. 1993X
  212349. 779-86Y
  212350. GABRIEL WEATHERHEAD
  212351. 15815
  212352. <AjFraser-Reid, B.//Udodong, U. E.//Wu, Z.//Ottosson, H.//Merritt, J. R.//Rao, C. S.//Roberts, C.//Madsen, R.B
  212353. SynlettM
  212354. 16824N
  212355. 2/28/96VRn-Pentenyl glycosides in organic chemistry: a contemporary example of serendipity.W
  212356. 1992X
  212357. GABRIEL WEATHERHEAD
  212358. 15816
  212359. =AsFraser-Reid, B.//Mootoo, D. R.//Konradsson, P.//Udodong, U. E.//Andr ws, C. W.//Ratcliffe, A. J.//Wu, Z.//Yu, K. L.B
  212360. Pure Appl. Chem.M
  212361. 16825N
  212362. 2/28/96VKNovel carbohydrate transformations discovered en route to natural products.W
  212363. 1989X
  212364. 1243Y
  212365. GABRIEL WEATHERHEAD
  212366. 15817
  212367. Franklin, A. S.//Paterson, I.B
  212368. Contemporary Organic SynthesisM
  212369. 16826N
  212370. 2/28/96V4Recent Developments in Asymmetric Aldol Methodology.W
  212371. 1994X
  212372. 317-338Y
  212373. GABRIEL WEATHERHEAD
  212374. 15818
  212375. Franek, W.B
  212376. Sulfur ReportsM
  212377. 16827N
  212378. 2/28/96Vm1,2,4,5-Tetrathianes. II. Structure and spectroscopic properties, electrochemistry, aroma  research and uses.W
  212379. 1991X
  212380. GABRIEL WEATHERHEAD
  212381. 15819
  212382. Franek, W.B
  212383. Sulfur ReportsM
  212384. 16828N
  212385. 2/28/96V11,2,4,5-Tetrathianes. I. Syntheses and reactions.W
  212386. 1991X
  212387. GABRIEL WEATHERHEAD
  212388. 15820
  212389. Fraga, B. M.B
  212390. Nat. Prod. Rep.M
  212391. 16829N
  212392. 2/28/96V
  212393. Natural sesquiterpenoids.W
  212394. 1993X
  212395. 397-419Y
  212396. GABRIEL WEATHERHEAD
  212397. 15821
  212398. BA!Fossey, J.//LeFort, D.//Sorba, J.B
  212399. Top. Curr. Chem.M
  212400. 16830N
  212401. 2/28/96VDPeracids and free radicals: a theoretical and experimental approach.W
  212402. 1993X
  212403. GABRIEL WEATHERHEAD
  212404. 15822
  212405. Forster, H.//Vogtle, F.
  212406. Angew. Chem., Int. Ed. Engl.C
  212407. PHYSICAL ORGANIC /MECHANISMSM
  212408. 16831N
  212409. 2/28/96VOSteric Interaction in Organic Chemistry: Spatial Requirements for Substituents.W
  212410. 1977X
  212411. GABRIEL WEATHERHEAD
  212412. 15823
  212413. DA!Freidlina, R. K.//Velichko, F. K.B    SynthesisC;C-C BOND FORMATION /APPENDAGES /MISCELLANEOUS /1,4-ADDITIONM
  212414. 16832N
  212415. 2/28/96V
  212416. Synthetic Applications of Homolytic Addition and Telomerisation Reactions of Bromine-Containi g Addends with Unsaturated Compounds Containing Electron-Withdrawing Substituents.W
  212417. 1977X
  212418. GABRIEL WEATHERHEAD
  212419. 15824
  212420. Freeman, P. K.//Hatlevig, S. A.B
  212421. Top. Curr. Chem.M
  212422. 16833N
  212423. 2/28/96V
  212424. The photochemistry of polyhalocompounds, dehalogenation by photoinduced electron transfer, new  methods of toxic waste disposal.W
  212425. 1993X
  212426. GABRIEL WEATHERHEAD
  212427. 15825
  212428. FAHFreeman, R.//Haynes, R. K.//Loughlin, W. A.//Mitchell, C.//Stokes, J. V.B
  212429. Pure Appl. Chem.C
  212430. P /SM
  212431. 16834N
  212432. 2/28/96
  212433. Synthetic utilization of highly stereoselective conjugate addition reactions of phosphorus and sulfur stabilized allylic carbanions.W
  212434. 1993X
  212435. GABRIEL WEATHERHEAD
  212436. 15826
  212437. Freeman, F.B
  212438. HeterocyclesC
  212439. 16835N
  212440. 2/28/96V!The chemistry of 4H-1,3-dithiins.W
  212441. 1990X
  212442. GABRIEL WEATHERHEAD
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  212444. HA,Freeman, F.//Kim, D. S. H. L.//Rodriguez, E.B
  212445. Sulfur ReportsC
  212446. 16836N
  212447. 2/28/96V
  212448. The chemistry of 1,2-dithiins.W
  212449. 1989X
  212450. GABRIEL WEATHERHEAD
  212451. 15828
  212452. Freeman, F.B    SynthesisCMFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /C-X(Y) /CN(CN) /MALONONITRILEM
  212453. 16837N
  212454. 2/28/96V'Reactions of Malononitrile Derivatives.W
  212455. 1981X
  212456. GABRIEL WEATHERHEAD
  212457. 15829
  212458. Freeman, F.B
  212459. Chem. Rev.C.FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUSM
  212460. 16838N
  212461. 2/28/96V2Properties and Reactions of Ylidenemalononitriles.W
  212462. 1980X
  212463. GABRIEL WEATHERHEAD
  212464. 15830
  212465. Freedman, L. D.//Doak, G. O.B
  212466. Chem. Rev.
  212467. ORGANOMETALLICS /BISMUTH /BiM
  212468. 16839N
  212469. 2/28/96VKPreparation, Reactions, and Physical Properties of Organobismuth Compounds.W
  212470. 1982X
  212471. GABRIEL WEATHERHEAD
  212472. 15831
  212473. Frechet, J.B
  212474. TetrahedronCCODDS AND ENDS /TECHNIQUES AND METHODS /ORGANIC POLYMERS /PROTECTIONM
  212475. 16840N
  212476. 2/28/96VQSynthesis and Applications of Organic Polymers as Supports and Protecting Groups.W
  212477. 1981X
  212478. GABRIEL WEATHERHEAD
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  212480. Frauenrath, H.B    SynthesisC
  212481. FUNCTIONAL GROUPS /PREPARATIONS /ETHERS AND ACETALS /1,3-DIOXOLES  /4-METHYLENE-1,3-DIOXOLANES /4H-1,3-DIOXINS /4-METHYLENE-1,3-DIOXANES  /4,5-DIHYDRODIOXEPINS /C=C-X /O /REARRANGEMENTS /FRAGMENTATION /FURANS /HETRING  /5(O) /CARBRING /4M
  212482. 16841N
  212483. 2/28/96V9Vinyl acetals and related compounds in organic synthesis.W
  212484. 1989X
  212485. GABRIEL WEATHERHEAD
  212486. 15833
  212487. NA*Frost, C.//Howarth, J.//William , J. M. J.B
  212488. Tetrahedron: AsymmetryC
  212489. 16842N
  212490. 2/28/96V8Selectivity in palladium catalyzed allylic substitution.W
  212491. 1992X
  212492. 1089Y
  212493. GABRIEL WEATHERHEAD
  212494. 15834
  212495. OACFronza, G.//Fuganti, C.//Grasselli, P.//Pedrocchi, F. G.//Servi, S.B
  212496. Pure Appl. Chem.M
  212497. 16843N
  212498. 2/28/96VIMinor synthetic capacities of bakers' yeast towards unnatural substrates.W
  212499. 1 92X
  212500. 1099Y
  212501. GABRIEL WEATHERHEAD
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  212503. Froman, M. A.B
  212504. Org. Prep. Proced. Int.M
  212505. 16844N
  212506. 2/28/96V>The synthesis and reactions of prismanes. Recent developments.W
  212507. 1994X
  212508. 291-320Y
  212509. GABRIEL WEATHERHEAD
  212510. 15836
  212511. QA3Fringuelli, F.//Minuti, L.//Pizzo, F.//Taticchi, A.B
  212512. Acta Chem. Scand.M
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  212514. 2/28/96V]Reactivity and selectivity in Lewis acid-catalyzed Diels-Alder reactions of 2-cyclohexenones.W
  212515. 1993X
  212516. 255-63Y
  212517. GABRIEL WEATHERHEAD
  212518. 15837
  212519. RA)Fringuelli, F.//Taticchi, A.//Wenkert, E.B
  212520. Org. Prep. Proced. Int.CLC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADD TIONS /[4+2] /CARBRING /6M
  212521. 16846N
  212522. 2/28/96VGDiels-Alder reactions of cycloalkenones in organic synthesis. A review.W
  212523. 1990X
  212524. GABRIEL WEATHERHEAD
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  212526. Friedrich, H. B.//Moss, J. R.B
  212527. Adv. Organomet. Chem.  33C
  212528. 16847N
  212529. 2/28/96V-Halogenoalkyl complexes of transition metals.W
  212530. 1991X
  212531. GABRIEL WEATHERHEAD
  212532. 15839
  212533. TA-Fridman, A. L.//Surkov, V. D.//Novikov, S. S.B Russ. Chem. Rev. (Engl. Transl.)CUFUNCTIONAL GROUPS  PREPARATIONS /MISCELLANEOUS /C-X(Y) /Cl(NO2) /HALOGENONITROALKANESM
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  212535. 2/28/96V
  212536. alpha-Halogenonitroalkanes.W
  212537. 1980X
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  212539. GABRIEL WEATHERHEAD
  212540. 15840
  212541. Fukuto, J. M.//Jensen, F. R.B
  212542. Acc. Chem. Res.C;ORGANOMETALLICS /TIN /PHYSICAL ORGANIC /MECHANISMS /SE2 /SnM
  212543. 16849N
  212544. 2/28/96V=Mechanisms of SE2 Reactions: Emphasis on Organotin Compounds.W
  212545. 1983X
  212546. GABRIEL WEATHERHEAD
  212547. 15841
  212548. VA%Fujiwara, Y.//Iintoku, T.//Takaki, K.B
  212549. CHEMTECHC
  212550. 16850N
  212551. 2/28/96V
  212552. Look what palladium catalyzes.W
  212553. 1990X
  212554. GABRIEL WEATHERHEAD
  212555. 15842
  212556. WACFujiwara, J.//Fukutani, Y.//Hasegawa, M.//Maruoka, K.//Yamamoto, H.B
  212557. ORGANOMETALLICS /ALUMINIUM /ENANTIOGENIC /CHIRAL AUXILIARY /C=C-C-X(Y) /O(O)  /C=C-CHO /SN2 /ADDITION /REGIOSELECTIVE /ENANTIOSELECTIVE /C=C-X-R /O C /AlM
  212558. 16851N
  212559. 2/28/96V
  212560. Regio- and Enantiocontrolled Addition of Organoaluminium Reagents to Chiral alpha,  beta-Unsaturated Aldehydes with Chiral Centres Using Chiral Auxiliaries.W
  212561. 1984X
  212562. 5004Y
  212563. GABRIEL WEATHERHEAD
  212564. 15843
  212565. Fujita, E.//Nagao, Y.B
  212566. Adv. Heterocycl. Chem.M
  212567. 16852N
  212568. 2/28/96V$Chiral inductio  using heterocycles.W
  212569. 1989X
  212570. GABRIEL WEATHERHEAD
  212571. 15844
  212572. YA"Fujii, T.//Ohba, M.//Yoshifuji, S.B
  212573. HeterocyclesC7TARGET SYNTHESIS /ALKALOIDS /HETEROCYCLES /LACTIM ETHERM
  212574. 16853N
  212575. 2/28/96VBChiral Synthesis of Benzo[a]quinolizidine-Type Apangium Alkaloids.W
  212576. 1988X
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  212578. GABRIEL WEATHERHEAD
  212579. 15845
  212580. Fuji, K.B
  212581. Chem. Rev.M
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  212583. 2/28/96V1Asymmetric creation of quaternary carbon centers.W
  212584. 1993X
  212585. 2037-66Y
  212586. GABRIEL WEATHERHEAD
  212587. 15846
  212588. Fuji, K.//Node, M.B
  212589. SynlettM
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  212591. 2/28/96V4Chiral nitro olefins for enantioselective reactions.W
  212592. 1991X
  212593. GABRIEL WEATHERHEAD
  212594. 15847
  212595. \A    Fuchs, B.B
  212596. Top. Stereochem.C<PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATION /C RBRING /5M
  212597. 16856N
  212598. 2/28/96V%Conformations of Five-Membered Rings.W
  212599. 1978X
  212600. GABRIEL WEATHERHEAD
  212601. 15848
  212602. Fuchigami, T.B
  212603. Top. Curr. Chem.C
  212604. 16857N
  212605. 2/28/96V4Electrochemical Reactions Of Fluoroorganic CompoundsW
  212606. 1994X
  212607. 1-37Y
  212608. GABRIEL WEATHERHEAD
  212609. 15849
  212610. Fu, X.//Cook, J. M.B
  212611. Aldrichimica ActaM
  212612. 16858N
  212613. 2/28/96VFThe synthesis of polyquinanes and polyquinenes via the Weiss reaction.W
  212614. 1992X
  212615. GABRIEL WEATHERHEAD
  212616. 15850
  212617. Fryzuk, M. D.B
  212618. Chem. Scr.C
  212619. ORGANOMETALLICS /ZIRCONIUM /ZrM
  212620. 16859N
  212621. 2/28/96VOFunctionalization of alkynes, enynes and arynes using organozirconium reagents.W
  212622. 1989X
  212623. GABRIEL WEATHERHEAD
  212624. 15851
  212625. Fry, A. J.B
  212626. Aldrichimica ActaM
  212627. 16860N
  212628. 2/28/96V&Electrochemistry in organic synthesis.W
  212629. 1993X
  212630. GABRIEL WEATHERHEAD
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  212632. aA    Gante, J.B
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  212637. GABRIEL WEATHERHEAD
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  212641. 2/28/96V
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  212644. GABRIEL WEATHERHEAD
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  212647. TetrahedronM
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  212649. 2/28/96V-The chemistry of 2-oxazolines (1985-present).W
  212650. 1994X
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  212652. GABRIEL WEATHERHEAD
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  212654. Ganem, B.//Henion, J. D.B
  212655. Chemtracts: Organic ChemistryM
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  212657. 2/28/96VnDetecting non ovalent complexes of biological macromolecules: new applications of ion-spray mass spectrometry.W
  212658. 1993X
  212659. 1-22Y
  212660. GABRIEL WEATHERHEAD
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  212662. eA    Galli, C.B
  212663. Org. Prep. Proced. Int.C
  212664. 16865N
  212665. 2/28/96V)'Cesium ion effect' and macrocyclization.W
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  212667. GABRIEL WEATHERHEAD
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  212669. Fuson, R. C.//McKeever, C. H.B
  212670. Org. React. (N.Y.)M
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  212672. 2/28/96
  212673. fV(Chloromethylation of Aromatic Compounds.W
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  212675. GABRIEL WEATHERHEAD
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  212677. Furstner, A.B
  212678. Angew. Chem., Int. Ed. Engl.M
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  212680. 2/28/96V-Chemistry of and with highly reactive metals.W
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  212686. 2/28/96VWPhosphorus-containing nucleophiles in reactions with polyfluorinated organic compounds.W
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  212688. GABRIEL WEATHERHEAD
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  212691. Chem. Soc. Rev.C^C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /ANNULATION /DA  /STEROIDS /CoM
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  212696. GABRIEL WEATHERHEAD
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  212699. Acta Chem. Scand.M
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  212701. 2/28/96
  212702. jVrIntramolecular cyclizations and ring-cleavage reactions of five-membered heteroarylnitrenes and  their precursors.W
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  212705. GABRIEL WEATHERHEAD
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  212707. Gawley, R. E.B
  212708. Org. React. (N.Y.)CBNAME REACTIONS /BECKMANN REARRANGEMENT /ELIMINATION /FRAGMENTATIONM
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  212710. 2/28/96VpThe Beckmann Reactions: Rearrangements, Elimination- Additions, Fragmentations, and  Rearrangement-Cyclisations.W
  212711. 1987X
  212712. GABRIEL WEATHERHEAD
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  212714. Gawley, R. E.B    SynthesisC<C-C BOND FORMATION /ANNULATIONS /6-RING /ROBINSON ANNELATIONM
  212715. 16872N
  212716. 2/28/96V.The Robinson Annelation and Related Reactions.W
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  212718. GABRIEL WEATHERHEAD
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  212721. HeterocyclesM
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  212723. 2/28/96VPSynthesis of Vicinally-Substituted Nitropyridine Derivatives and Their N-Oxides.W
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  212725. GABRIEL WEATHERHEAD
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  212740. GABRIEL WEATHERHEAD
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  212743. Acc. Chem. Res.CFPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONSM
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  212745. 2/28/96V Electron-Deficient Carbocations.W
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  212747. GABRIEL WEATHERHEAD
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  212752. 2/28/96VMThe T ermal Addition of Carbon-Carbon Multiple Bonds to Strained Carbocycles.W
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  212754. GABRIEL WEATHERHEAD
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  212763. GABRIEL WEATHERHEAD
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  212765. sA%Gasc, M. B.//Lattes, A.//Perie, J. J.B
  212766. TetrahedronCHFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /C=C /AMINATION /AMINES /C-X /NM
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  212771. GABRIEL WEATHERHEAD
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  212777. 2/28/96VFGrignard reagent formation and freely diffusing radica  intermediates.W
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  212779. GABRIEL WEATHERHEAD
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  212784. 2/28/96V$Battered benzene and twisted ethene.W
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  212786. GABRIEL WEATHERHEAD
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  212791. 2/28/96VIPossible surface intermediates in alkane reactions on metallic catalysts.W
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  212798. 2/28/96VYSaccharides of biological importance: challenges and opportunities for organic synthesis.W
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  212800. GABRIEL WEATHERHEAD
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  212802. Garcia, F.//Galvez, C.B    SynthesisCgC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /PYRROLE HETRING /5(N)  THIOPHENE HETRING /5(S)M
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  212804. 2/28/96V The Synthesis  f Thienopyrroles.W
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  212806. GABRIEL WEATHERHEAD
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  212811. 2/28/96VSOligodeoxyguanylates: a case of self-assembly leading to lyotropic liquid crystals.W
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  212814. GABRIEL WEATHERHEAD
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  212844. 2/28/96V/Nickel Peroxide Oxidation of Organic Compounds.W
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  212851. 2/28/96V=Migratory-insertion of carbon monoxide into metal-acyl bonds.W
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  212866. 2/28/96V@The Synthesis of Isoquinolines by the Pomeranz-Fritsch Reaction.W
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  212873. 2/28/96V:The Reactivity of Cyclic Acetals of Aldoses and Aldosides.W
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  212879. 2/28/96V%Pentacoordinate fluorosilicate anion.W
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  212959. GABRIEL WEATHERHEAD
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  212964. 2/28/96V(The Gabriel Synthesis of Primary Amines.W
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  212997. 2/28/96V&Chiral amides in asymmetric synthesis.W
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  213005. 2/28/96VHThe structure-directed synthesis of cyclacene and polyacene derivatives.W
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  213022. Small Ring Propellanes.W
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  213029. 2/28/96V)Carboranylcarbenes and dehydrocarboranes.W
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  213039. GABRIEL WEATHERHEAD
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  213045. 2/28/96VZDisplacement Reactions of Phosphorus(V) Compounds and Their Pentacoordinate Intermediates.W
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  213052. 2/28/96VYStructurally Characterized Organometallic Hydroxo Complexes of the f- and d-Block Metals.W
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  213054. 895-910Y
  213055. GABRIEL WEATHERHEAD
  213056. 15908
  213057. Gilday, J. P.//Paquette, L. A.B
  213058. Org. Prep. Proced. Int.C
  213059. NAME REACTIONSM
  213060. 16917N
  213061. 2/28/96VFCarbon-c rbon bond cleavage by the Haller-Bauer and related reactions.W
  213062. GABRIEL WEATHERHEAD
  213063. 15909
  213064. Gilchrist, T. L.B
  213065. Contemporary Organic SynthesisM
  213066. 16918N
  213067. 2/28/96V1Synthesis of five-membered aromatic heterocycles.W
  213068. 1994X
  213069. GABRIEL WEATHERHEAD
  213070. 15910
  213071. Gilchrist, T. L.B
  213072. Chem. Soc. Rev.CdFUNCTIONAL GROUPS /PREPARATIONS /HETEROALKENES /C=C-X /NO /CC-X /NO  /NITROSOALKENES /NITROSOALKYNESM
  213073. 16919N
  213074. 2/28/96V$Nitroso-alkenes and Nitroso-alkynes.W
  213075. 1983X
  213076. GABRIEL WEATHERHEAD
  213077. 15911
  213078. Gilchrist, T. L.//Moody, C. J.B
  213079. Chem. Rev.CIFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /SULFIL MINES /SM
  213080. 16920N
  213081. 2/28/96V
  213082. The Chemistry of Sulfilimines.W
  213083. 1977X
  213084. GABRIEL WEATHERHEAD
  213085. 15912
  213086. Gokel, G. W.//Durst, H. D.B    SynthesisC3ODDS AND ENDS /TECHNIQUES AND METHODS /CROWN ETHERSM
  213087. 16921N
  213088. 2/28/96V?Principles and Synthetic Applications in Crown Ether Chemistry.W
  213089. 1976X
  213090. GABRIEL WEATHERHEAD
  213091. 15913
  213092. Goethe, J. W.B
  213093. Synform
  213094. C!TARGET SYNTHESIS /TOTAL SYNTHESISM
  213095. 16922N
  213096. 2/28/96V
  213097. Pentalenolactones.W
  213098. 1989X
  213099. GABRIEL WEATHERHEAD
  213100. 15914
  213101. Gocmen, A.//Bulut, M.//Erk, C.B
  213102. Pure Appl. Chem.M
  213103. 16923N
  213104. 2/28/96V8Synthesis and characterization of coumarin-crown ethers.W
  213105. 1993X
  213106. 447-50Y
  213107. GABRIEL WEATHERHEAD
  213108. 15915
  213109. Gleiter, R.//Kratz, D.B
  213110. Angew. Chem., Int. Ed. Engl.M
  213111. 16924N
  213112. 2/28/96V7Conjugated enediynes-an old topic in a different light.W
  213113. 1993X
  213114. 842-45Y
  213115. GABRIEL WEATHERHEAD
  213116. 15916
  213117. Gleiter, R.//Kratz, D.B
  213118. Acc. Chem. Res.M
  213119. 16925N
  213120. 2/28/96V
  213121. 'Super' phanes.W
  213122. 1993X
  213123. 311-18Y
  213124. GABRIEL WEATHERHEAD
  213125. 15917
  213126. Gleiter, R.B
  213127. Angew. Chem., Int. Ed. Engl.M
  213128. 16926N
  213129. 2/28/96VBCycloalkadiynes-from bent triple bonds to strain d cage compounds.W
  213130. 1992X
  213131. GABRIEL WEATHERHEAD
  213132. 15918
  213133. Gleiter, R.//Schaefer, W.B
  213134. Acc. Chem. Res.M
  213135. 16927N
  213136. 2/28/96V-Interactions between nonconjugated  -systems.W
  213137. 1990X
  213138. GABRIEL WEATHERHEAD
  213139. 15919
  213140. Gleiter, R.//Paquette, L. A.B
  213141. Acc. Chem. Res.C-PHYSICAL ORGANIC /STEREOELECTRONICS /ADDITIONM
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  213143. 2/28/96VXs /p Interaction as a Controlling Factor in the Stereoselectivity of Addition Reactions.W
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  213145. GABRIEL WEATHERHEAD
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  213149. 2/28/96VmSyntheses of organic compounds in the presence of the fused iron catalyst and their mechanisms and  kinetics.W
  213150. 1989X
  213151. GABRIEL WEATHERHEAD
  213152. 15921
  213153. Gladysz, J. A.B
  213154. Acc. Chem. Res.C,ORGANOMETALLICS /SILICON /R3SiH /C-M /Si /TMM
  213155. 16930N
  213156. 2/28/96VENew Synthetic Chemistry of T ansition Metal Trialkylsilane Complexes.W
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  213158. GABRIEL WEATHERHEAD
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  213163. 2/28/96V#Photochemistry of phosphate esters.W
  213164. 1993X
  213165. GABRIEL WEATHERHEAD
  213166. 15923
  213167. A*Gonzalez, A. G.//Galindo, A.//Mansilla, H.B
  213168. HeterocyclesM
  213169. 16932N
  213170. 2/28/96
  213171. V5Biomimetic transformations of sesquiterpene lactones.W
  213172. 1989X
  213173. GABRIEL WEATHERHEAD
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  213175. A.Golubev, A. S.//Kolomiets, A. F.//Fokin, A. V.B Russ. Chem. Rev. (Engl. Transl.)C
  213176. 16933N
  213177. 2/28/96V:Reactions of polyfluoroketones with unsaturated compounds.W
  213178. 1992X
  213179. GABRIEL WEATHERHEAD
  213180. 15925
  213181. A!Gololobov, Y. G.//Kasukhin, L. F.B
  213182. TetrahedronM
  213183. 16934N
  213184. 2/28/96V+Recent advances in the Staudinger reaction.W
  213185. 1992X
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  213187. GABRIEL WEATHERHEAD
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  213189. A2Gololobov, Y. G.//Lysenko, V. P.//Boldeskul, I. E.B
  213190. TetrahedronC
  213191. REAGENTS /H2C=S(O)Me2 /DIMETHYLSULFOXONIUM METHYLIDE /COREY'S REAGENT /O=C-H  /O=C-R /ALDEHYDES /KETONES /ENONES /O=C-C=C /1 /CYCLOADDITION /[1,2] /[1,4]  /CYCLOPROPANATION /HETRING /3(O) /CARBRING /3 /OXIRANES /CYCLOPROPANESM
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  213193. 2/28/96VETwenty-five Years of Dimethylsulfoxonium Methylide (C rey's Reagent).W
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  213195. 2609Y
  213196. GABRIEL WEATHERHEAD
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  213198. Golebiowski, A.//Jurczak, J.B
  213199. SynlettM
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  213201. 2/28/96VFalpha-Amino-beta-hydroxy acids in the total synthesis of amino sugars.W
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  213204. GABRIEL WEATHERHEAD
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  213206. Goldschmidt, Z.//Crammer, B.B
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  213208. C-C BOND FORMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[1,3] /ANNULATIONS /5-RING  /CARBRING /3 /VINYLCYCLOPROPANE /REARRANGEMENT /CARBRING /5M
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  213210. 2/28/96V!Vinylcyclopropane Rearrangements.W
  213211. 1988X
  213212. GABRIEL WEATHERHEAD
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  213217. 2/28/96Vy1,4-Dihydropyridines: effect of chirality and conformation on the calcium antagonistic and calcium  agonistic activities.W
  213218. 1991X
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  213220. GABRIEL WEATHERHEAD
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  213222. A*Goldberg, Y.//Styrkovich, R.//Lukevics, E.B
  213223. HeterocyclesC
  213224. ODDS AND ENDS /TECHNIQUES AND METHODS /HETEROCYCLES /INDOLE /FURAN /THIOPHENE  /BARBIER /SONOCHEMISTRY /
  213225. -LACTAM /Mg /Zn /Li /Cu /KM
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  213227. 2/28/96V
  213228. Heterocyclic Sonochemistry.W
  213229. 1989X
  213230. GABRIEL WEATHERHEAD
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  213233. Top. Curr. Chem.M
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  213235. 2/28/96VUThe significance of molecular type, shape and complementarity in clathrate inclusion.W
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  213241. 2/28/96V`Reactions of hydrocarbons with electrophilic transition metal complexes in trifluoroacetic acid.W
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  213243. GABRIEL WEATHERHEAD
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  213246. Chem. Soc. Rev.M
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  213248. 2/28/96V>Lariat ethers: from simple sidearms to supramolecular systems.W
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  213255. 2/28/96VELariat ethers: from cation complexation to supramolecular assemblies.W
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  213257. GABRIEL WEATHERHEAD
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  213259. A:Gokel, G. W.//Dishong, D. M.//Schultz, R. A.//Gatto, V. J.B    Synthesis
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  213261. 16944N
  213262. 2/28/96V*Syntheses of Aliphatic Azacrown Compounds.W
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  213264. GABRIEL WEATHERHEAD
  213265. 15936
  213266. A%Grasso, S.//Zappala, M.//Chimizzi, A.B
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  213269. 2/28/96V
  213270. Benzodiazocines.W
  213271. 1987Y
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  213276. J. Organomet. Chem.C9ORGANOMETALLICS /GENERAL /TIN /Ir /Re /Os /Si /Sn /Ge /PbM
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  213278. 2/28/96V4From silicon-hydrogen to carbon-hydrogen activation.W
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  213280. GABRIEL WEATHERHEAD
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  213283. Top. Stereochem.M
  213284. 16947N
  213285. 2/28/96V)Anomeric effect: origin and consequences.W
  213286. 1994X
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  213288. GABRIEL WEATHERHEAD
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  213291. Pure Appl. Chem.M
  213292. 16948N
  213293. 2/28/96
  213294. ViRecent aspects of glycoconjugate synthesis: a synthetic approach to the linkage region of  proteoglycans.W
  213295. 1993X
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  213300. Chem. Soc. Rev.C^ORGANOME ALLICS /SULPHUR /SUBSTITUTION /O BY N /SN1 /SN2 /SAN /SULPHONYL TRANSFER REACTIONS /SM
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  213302. 2/28/96V
  213303. Sulphonyl Transfer Reactions.W
  213304. 1989X
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  213308. TetrahedronM
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  213310. 2/28/96V'Chemistry of chlorocarbonyl isocyanate.W
  213311. 1993X
  213312. 3227-57Y
  213313. GABRIEL WEATHERHEAD
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  213317. 2/28/96V7Synthesis and Reactions of alpha-Haloalkyl Isocyanates.W
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  213324. V*The Synthesis of alpha-Methylene Lactones.W
  213325. 1975X
  213326. GABRIEL WEATHERHEAD
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  213329. Contemporary Organic SynthesisM
  213330. 16953N
  213331. 2/28/96VLRecent developments in indole ring synthesis - methodology and applications.W
  213332. 1994X
  213333. GABRIEL WEATHERHEAD
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  213335. Gribble, G. W.B
  213336. SynlettM
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  213338. 2/28/96VGApproaches to the synthesis of  he antitumor pyridocarbazole alkaloids.W
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  213340. GABRIEL WEATHERHEAD
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  213343. Chem. Soc. Rev.CEFUNCTIONAL GROUPS /PREPARATIONS /HETEROALKENES /O=C-C=C-N /ENAMINONESM
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  213345. 2/28/96V
  213346. Enam nones.W
  213347. 1977X
  213348. GABRIEL WEATHERHEAD
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  213350. Greenberg, A.//Wu, G.B
  213351. Structural ChemistryM
  213352. 16956N
  213353. 2/28/96V0Structural relationships in silatrane molecules.W
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  213355. GABRIEL WEATHERHEAD
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  213357. Green, M. L. H.//Mountford, P.B
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  213361. 2/28/96V3Cyclopentadienyl molybdenum and tungsten dihalides.W
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  213363. GABRIEL WEATHERHEAD
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  213366. TetrahedronC.TARGET SYNTHESIS /PROSTAGLANDINS /LEUKOTRIENESM
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  213368. 2/28/96V
  213369. Leukotrienes.W
  213370. 1983X
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  213372. GABRIEL WEATHERHEAD
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  213374. Gree, R.B    SynthesisC>ORGANOMETALLICS /ORGANIC SYNTHESIS /IRON /[C=C-C=C]Fe(CO)3 /FeM
  213375. 16959N
  213376. 2/28/96VBAcyclic Butadiene-Iron Tricarbonyl Complexes in Organic Synthesis.W
  213377. 1989X
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  213380. A(Grebenik, P.//Grinter, R.//Perutz, R. N.B
  213381. Chem. Soc. Rev.C+ORGANOMETALLICS /GENERAL /C-M / ETALLOCENESM
  213382. 16960N
  213383. 2/28/96V'Metallocenes as Reaction Intermediates.W
  213384. 1988X
  213385. GABRIEL WEATHERHEAD
  213386. 15952
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  213388. Nat. Prod. Rep.M
  213389. 16961N
  213390. 2/28/96V
  213391. Monoterpenoids.W
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  213396. Chem. Rev.C
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  213398. 2/28/96V6Boron-carbon ring ligands in organometallic synthesis.W
  213399. 1992X
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  213402. Grimes, R. N.B
  213403. Pure Appl. Chem.C
  213404. 16963N
  213405. 2/28/96
  213406. VISmall carboranes as building blocks in designed organometallic synthesis.W
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  213410. A!Grigor'eva, N. Y.//Pinsker, O. A.B Russ. Chem. Rev. (Engl. Transl.)M
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  213412. 2/28/96VeNew methods of synthesis of linear functionalized (Z)-isoprenoids and their  2,3-dihydro-derivatives.W
  213413. 1994X
  213414. GABRIEL WEATHERHEAD
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  213416. A    Grigg, R.B
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  213420. 2/28/96VuPrototropic Routes to 1,3- and 1,5-Dipoles, and 1,2-Ylides: Applications to the Synthesis of  Heterocyclic Compounds.W
  213421. 1987X
  213422. GABRIEL WEATHERHEAD
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  213424. Grigat, E.B
  213425. Angew. Chem., Int. Ed. Engl.C=FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /CYANIC ESTERSM
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  213427. 2/28/96V
  213428. New Reactions of Cyanic Esters.W
  213429. 1972X
  213430. GABRIEL WEATHERHEAD
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  213432. Griffiths, W. P.B
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  213435. 2/28/96V,Ruthenium oxo complexes as organic oxidants.W
  213436. 1992X
  213437. GABRIEL WEATHERHEAD
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  213439. Griffith, W. P.//Ley, S. V.B
  213440. Aldrichimica ActaC<FUNCTIONAL GROUPS /OXIDATION /CH-OH TO C=O /C-X /OH /C=O /RuM
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  213442. 2/28/96VVTPAP: Tetra-n-propylammonium perruthenate, a mild and convenient oxidant for alcohols.W
  213443. 1990X
  213444. GABRIEL WEATHERHEAD
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  213446. Griffin, G. W.//Marchand, A. P.B
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  213449. 16969N
  213450. 2/28/96V#Synthesis and Chemistry of Cubanes.W
  213451. 1989X
  213452. GABRIEL WEATHERHEAD
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  213454. Grierson, D.B
  213455. Org. React. (N.Y.)C
  213456. NAME REACTIONSM
  213457. 16970N
  213458. 2/28/96V
  213459. The Polonovski reaction.W
  213460. 1990X
  213461. GABRIEL WEATHERHEAD
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  213463. Grieco, P. A.B
  213464. Aldrichimica ActaM
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  213466. 2/28/96V-Organic chemistry  n unconventional solvents.W
  213467. 1991X
  213468. GABRIEL WEATHERHEAD
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  213470. Grossel, M. C.//Weston, S. C.B%Journal of Physical Organic ChemistryM
  213471. 16972N
  213472. 2/28/96VGSupramolecular control of molecular electronic behaviour of TCNQ salts.W
  213473. 1992X
  213474. GABRIEL WEATHERHEAD
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  213476. Gross, H.//Hoft, E.B
  213477. Angew. Chem., Int. Ed. Engl.CXC-C BOND FORMATION /APPENDAGES /ALKYLATION /C-X(Y) /Cl(O) /C-X(Y) /Cl(S) /C-X(Y)  /Cl(N)M
  213478. 16973N
  213479. 2/28/96VXThe Formation of C-C Bonds with the Aid of alpha-Halogeno Ethers, Sulphides, and Amines.W
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  213481. GABRIEL WEATHERHEAD
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  213483. Gromov, S. P.//Kos , A. N.B
  213484. HeterocyclesM
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  213495. 2/28/96VLFrom polyenals to retinal: an electron-spin-echo study of the triplet state.W
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  213497. GABRIEL WEATHERHEAD
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  213499. Grobel, B. T.//Seebach, D.B    SynthesisC
  213500. ODDS AND ENDS /STRATEGIES AND THEORY OF SYNTHESIS /SYNTHONS /C-X(Y) /S(S) /C=C-X(Y)  /S(S) /DITHIANES /THIOACETALES /ALKYLATION /ADDITION /UMPOLUNG /O=C-H /O=C-R  /ALDEHYDES /KETONES /SM
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  213502. 2/28/96VUUmpolung of the Reactivity of Carbonyl Compounds Through Sulphur-Containing Reagents.W
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  213504. GABRIEL WEATHERHEAD
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  213506. Grob, C. A.B
  213507. Acc. Chem. Res.CFPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONSM
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  213509. 2/28/96V)Inductivity and Bridging in Carbocations.W
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  213511. GABRIEL WEATHERHEAD
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  213514. Angew. Chem., Int. Ed. Engl.C
  213515. PHYSICAL ORGANIC /MECHANISMSM
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  213517. 2/28/96V#Polar Effects in Organic Reactions.W
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  213519. GABRIEL WEATHERHEAD
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  213521. Grob, C. A.B
  213522. Angew. Chem., Int. Ed. Engl.CHPHYSICAL ORGANIC /MECHANISMS /STEREOCHEMISTRY /HETEROLYTIC FRAGMENTATIONM
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  213524. 2/28/96V=Mechanisms and Stereochemistry of Heterolytic Fragmentations.W
  213525. GABRIEL WEATHERHEAD
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  213527. Grob, C. A.//Schiess, P. W.B
  213528. Angew. Chem., Int. Ed. Engl.C%MECHANISMS /HETEROLYTIC FRAGMENTATIONM
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  213530. 2/28/96V8Heterolytic Fragmentation. A Class of Organic Reactions.W
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  213532. GABRIEL WEATHERHEAD
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  213538. GABRIEL WEATHERHEAD
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  213543. 2/28/96V`Halogenation of heterocycles: III. Heterocycles fused to other aromatic or heteroaromatic rings.W
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  213545. GABRIEL WEATHERHEAD
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  213550. 2/28/96V@Halogenation of heterocycles: I . Six- and seven-membered rings.W
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  213558. 2/28/96V6Halogenation of heterocyclies: 1. Five-membered rings.W
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  213567. 2/28/96V<Reactions of annular nitrogens of azines with electrophiles.W
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  213569. GABRIEL WEATHERHEAD
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  213572. Chem. Soc. Rev.CWC-C BOND FORMATION /APPENDAGES /MISCELLANEOUS /NAME REACTIONS /C=C /ACYLATION  /O=C-C=CM
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  213574. 2/28/96V(The Friedel-Crafts Acylation of Alkenes.W
  213575. 1972X
  213576. GABRIEL WEATHERHEAD
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  213579. Angew. Chem., Int. Ed. Engl.C>ORGANOMETALLICS /LITHIUM /PHYSICAL ORGANIC /REARRANGEMENTS /LiM
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  213581. 2/28/96V8Skeletal Rearrangements of Organoalkali Metal Co pounds.W
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  213583. GABRIEL WEATHERHEAD
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  213585. Grove, J. F.B
  213586. Nat. Prod. Rep.M
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  213588. 2/28/96V
  213589. Macrocyclic trichothecenes.W
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  213594. Groutas, W. C.//Felker, D.B    SynthesisCJORGANOMETALLICS /SILICON /REAGENTS /Me3SiCN,Me3SiI,Me3SiN3,Me3SiSMe /Si /SM
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  213596. 2/28/96VzSynthetic Applications of Cyanotrimethylsilane, Iodotrimethylsilane, Azidotrimethylsilane, and  Methylthiotrimethylsilane.W
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  213598. GABRIEL WEATHERHEAD
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  213600. Grotjahn, D. B.//Dotz, K. H.B
  213601. SynlettM
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  213603. 2/28/96V<Carbene complexes of chromium hearing nitrogen substituents.W
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  213605. GABRIEL WEATHERHEAD
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  213609. 16991N
  213610. 2/28/96V=Synthesis of Materials for Molecular Electronic Applications.W
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  213613. GABRIEL WEATHERHEAD
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  213617. 2/28/96VGSynthesis, structure, and reactivity of alpha-(trihalomethyl)carbinols.W
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  213620. GABRIEL WEATHERHEAD
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  213625. 2/28/96V;New synthetic applications of dialkylboron halide reagents.W
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  213631. Acta Chem. Scand.M
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  213633. 2/28/96VGSynthesis and application of macrocyclic and macroacyclic Schiff bases.W
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  213636. GABRIEL WEATHERHEAD
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  213639. Bull.  oc. Chim. Fr.
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  213642. 2/28/96VMMononuclear and Dinuclear (Pentamethylcyclopentadienyl)Iron-Carbene ComplexesW
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  213650. 2/28/96V3Modern NMR Spectroscopy of Organolithium Compounds.W
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  213656. Chem.-Ztg.C2REAGENTS /METHYL ISOTHIOCYANATE /PREP /REACTION /SM
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  213658. 2/28/96VNMethyl Isothioc anate - from Natural Product to Commercial Synthetic Material.W
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  213660. GABRIEL WEATHERHEAD
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  213665. 2/28/96VOTaxol and taxotere: discovery, chemistry, and structure-activity relationships.W
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  213673. -Aminophosphonates and 
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  213676. GABRIEL WEATHERHEAD
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  213682. 2/28/96V#Heteroatom-Facilitated Lithiations.W
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  213684. GABRIEL WEATHERHEAD
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  213689. 2/28/96V5Compounds with three-membered rings containing boron.W
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  213697. 2/28/96VITransformations of Chloroarenes,  atalyzed by Transition-Metal Complexes.W
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  213706. The Nazarov Cyclization.W
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  213716. GABRIEL WEATHERHEAD
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  213719. Pure Appl. Chem.M
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  213721. 2/28/96VIGlycopeptides of biological interest: a challenge for chemical synthesis.W
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  213724. GABRIEL WEATHERHEAD
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  213727. TetrahedronC
  213728. FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /1,3,4-THIADIZOLINES  1,3,4-SELENADIAZOLINES HETRING /5(N,N,S) HETRING /5(N,N,Se) /EXTRUSION CHELOTROPIC /C=C  / LKENES /ALKYNES /ACETYLENES /CYCLOPHANES /S /Se /TeM
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  213730. 2/28/96V^Synthetically Useful Extrusion Reactions of Organic Sulfur, Selenium, and Tellurium Compounds.W
  213731. 1988X
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  213733. GABRIEL WEATHERHEAD
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  213735. Gutsche, C. D.B
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  213738. 2/28/96VLThe Reaction of Diazomethane and Its Derivatives with Aldehydes and Ketones.W
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  213740. GABRIEL WEATHERHEAD
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  213743. Pure Appl. Chem.M
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  213746. V:Calixarenes: paradoxes and paradigms in molecular baskets.W
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  213748. GABRIEL WEATHERHEAD
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  213753. 2/28/96V+Vinyl tellur des: synthesis and properties.W
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  213760. 2/28/96V:Divinyl sulfoxide synthesis, properties, and applications.W
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  213766. 2/28/96V5Synthesis of heterocycles by the aza-Wittig reaction.W
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  213768. GABRIEL WEATHERHEAD
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  213771. TetrahedronC
  213772. C-C BOND FORMATION /ANNULATIONS /5-RING /TARGET SYNTHESIS /UNNATURAL PRODUCT  /DICARBONYLS /1,2 /DICARBONYLS /1,3 /ANNULATION /5-RING /CARBRING /5M
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  213775. VJGeneral approach for the synthesis of polyquinenes via the Weiss reaction.W
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  213780. Halpern, J.B
  213781. Angew. Chem., Int. Ed. Engl.C(ORGANOMETALLICS /GENERAL /C-M /OXIDATIONM
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  213783. 2/28/96V&Oxidation of Organometallic Compounds.W
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  213785. GABRIEL WEATHERHEAD
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  213791. Biomimetic Chemistry Of NickelW
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  213798. 2/28/96VwStereochemical Aspects of Tellurium Complexes with Sulfur Ligands: Molecular Compou ds and Supramolecular Associations.W
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  213801. GABRIEL WEATHERHEAD
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  213804. HeterocyclesM
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  213806. 2/28/96
  213807. Recent advances in the chemistry of condensed pyridazines: synthesis of bi- and tricyclic systems  by annelation of five-, six-, and seven-membered rings to a preformed 1,2-diazine nucleus.W
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  213810. GABRIEL WEATHERHEAD
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  213815. 2/28/96V(The von Braun Cyanogen Bromide Reaction.W
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  213817. GABRIEL WEATHERHEAD
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  213822. 2/28/96V4Novel peric clic reactions in  -perimeter chemistry.W
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  213824. 17-25Y
  213825. GABRIEL WEATHERHEAD
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  213827. Hanson, J. R.B    SynthesisC
  213828. ORGANOMETALLICS /CHROMIUM /CrM
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  213830. 2/28/96V>Applications of Cr(II) Salts in Preparati e Organic Chemistry.W
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  213832. GABRIEL WEATHERHEAD
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  213835. Angew. Chem., Int. Ed. Engl.C/FUNCTIONAL GROUPS /REDUCTION /MISCELLANEOUS /CrM
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  213837. 2/28/96V5The Reduction of Organic Compounds with Cr(II) Salts.
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  213839. GABRIEL WEATHERHEAD
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  213844. 2/28/96V)Preparation of Ketenes and Ketene Dimers.W
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  213846. GABRIEL WEATHERHEAD
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  213849. Aldrichimica ActaCTFUNCTIONAL GROUPS /T ANSFORMATIONS /CARBOHYDRATES /USEFUL FRAGMENTS /STEREOCHEMISTRYM
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  213851. 2/28/96VoDesign and Implementation of Tactically Novel Strategies for Stereochemical Control Using the  Chiron Approach.W
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  213856. Angew. Chem., Int. Ed. Engl.C
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  213859. 2/28/96V>Mechanistic and Preparative Aspects of Vinyl Cation Chemistry.W
  213860. 1978X
  213861. GABRIEL WEATHERHEAD
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  213863. Hanack, M.B
  213864. Acc. Chem. Res.CFPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS
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  213866. 2/28/96V
  213867. Stabilised Vinyl Cations.W
  213868. 1976X
  213869. GABRIEL WEATHERHEAD
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  213871. Hamlin, K. E.//Weston, A. W.B
  213872. Org. React. (N.Y.)M
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  213874. 2/28/96V9The Cleavage of Non-enolizable Ketones with Sodium Amide.W
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  213876. GABRIEL WEATHERHEAD
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  213881. 2/28/96VeThe Preparation of Aromatic Arsonic and Arsinic Acids by the Bart, Bechamp, and Rosenmund  Reactions.W
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  213883. GABRIEL WEATHERHEAD
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  213886. Pure Appl. Chem.M
  213887. 17027N
  213888. 2/28/96V8Alkylidenecycloproparenes: strained and polar aromatics.W
  213889. 1990X
  213890. GABRIEL WEATHERHEAD
  213891. 16019
  213892. Halton, B.B
  213893. Chem. Rev.CLPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULES /CYCLOPROPARENEM
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  213895. 2/28/96V)Developments in Cycloproparene Chemistry.W
  213896. 1989X
  213897. 1161Y
  213898. GABRIEL WEATHERHEAD
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  213900. Halton, B.//Stang, P. J.B
  213901. Acc. Chem. Res.
  213902.     CEC-C BOND FORMATION /ANNULATIONS /3-RING /CYCLOPROPARENES /CARBRING /3M
  213903. 17029N
  213904. 2/28/96V0Alkylidenecycloproparenes and Related Compounds.W
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  213906. GABRIEL WEATHERHEAD
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  213909. Chem. Rev.C~PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULES /C-C BOND FORMATION  /AROMATICS /RING /CARBRING /3 /CYCLOPROPENESM
  213910. 17030N
  213911. 2/28/96V
  213912. Benzocyclopropenes.W
  213913. 1973X
  213914. GABRIEL WEATHERHEAD
  213915. 16022
  213916. Halterman, R. L.B
  213917. Chem. Rev.M
  213918. 17031N
  213919. 2/28/96VESynthesis and applications of chiral cyclopentadienylme al complexes.W
  213920. 1992X
  213921. GABRIEL WEATHERHEAD
  213922. 16023
  213923. Harper, D. B.//Ohagan, D.B
  213924. Nat. Prod. Rep.C
  213925. 17032N
  213926. 2/28/96V The Fluorinated Natural-ProductsW
  213927. 1994X
  213928. 123-133Y
  213929. GABRIEL WEATHERHEAD
  213930. 16024
  213931. Harmange, J.-C.//Figadere, B.B
  213932. Tetrahedron: AsymmetryM
  213933. 17033N
  213934. 2/28/96V7Synthetic routes to 2,5-disubstituted tetrahydrofurans.W
  213935. 1993X
  213936. 1711-54Y
  213937. GABRIEL WEATHERHEAD
  213938. 16025
  213939. A)Harman, R. E.//Gupta, S. K.//Brown, D. J.B
  213940. Chem. Rev.CmFUNCTIONAL GROUPS /CATALYTIC HYDROGENATION /C=C /ALKENES /REDUCTION /HOMOGENEOUS  HYDROGENATION /C-C /ALKANESM
  213941. 17034N
  213942. 2/28/96V?Hydrogenation of Organic Compounds Usi g Homogeneous Catalysis.W
  213943. 1973X
  213944. GABRIEL WEATHERHEAD
  213945. 16026
  213946. Harada, T.//Oku, A.B
  213947. SynlettM
  213948. 17035N
  213949. 2/28/96V`Enantiodifferentiating transformation of prochiral polyols by using menthone as chiral template.W
  213950. 1994X
  213951. 95-104a
  213952. GABRIEL WEATHERHEAD
  213953. 16027
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  213955. Chem. Rev.C
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  213957. 17036N
  213958. 2/28/96VPLigand influences on structure and reactivity in organoalkaline earth chemistry.W
  213959. 1993X
  213960. 1023-36Y
  213961. GABRIEL WEATHERHEAD
  213962. 16028
  213963. Hanson, J. R.B
  213964. Nat. Prod. Rep.M
  213965. 17037N
  213966. 2/28/96V
  213967. Diterpenoids.W
  213968. 1993X
  213969. 159-74Y
  213970. GABRIEL WEATHERHEAD
  213971. 16029
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  213973. Nat. Prod. Rep.M
  213974. 17038N
  213975. 2/28/96V4Stevioside and related sweet diterpenoid glycosides.W
  213976. 1993X
  213977. 301-9Y
  213978. GABRIEL WEATHERHEAD
  213979. 16030
  213980. Hanson, J. R.B
  213981. Nat. Prod. Rep.M
  213982. 17039N
  213983. 2/28/96V(Steroid reactions and partial synthesis.W
  213984. 1993X
  213985.  313-25Y
  213986. GABRIEL WEATHERHEAD
  213987. 16031
  213988. Hanson, J. R.B
  213989. Nat. Prod. Rep.M
  213990. 17040N
  213991. 2/28/96V*Steroids: reactions and partial syntheses.W
  213992. 1992X
  213993. GABRIEL WEATHERHEAD
  213994. 16032
  213995. Hanson, J. R.B
  213996. Nat. Prod. Rep.M
  213997. 17041N
  213998. 2/28/96V
  213999. The sesterterpenoids.W
  214000. 1992X
  214001. GABRIEL WEATHERHEAD
  214002. 16033
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  214004. Nat. Prod. Rep.M
  214005. 17042N
  214006. 2/28/96V3The microbiological transformation of diterpenoids.W
  214007. 1992X
  214008. GABRIEL WEATHERHEAD
  214009. 16034
  214010. Hanson, R. M.B
  214011. Chem. Rev.CZFUNCTIONAL GROUPS /TRANSFORMATIONS /EPOXIDE CLEAVAGE / ETRING /3(O) /SHARPLESS EPOXIDATIONM
  214012. 17043N
  214013. 2/28/96VPThe synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols.W
  214014. 1991X
  214015. GABRIEL WEATHERHEAD
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  214017. Hart, H.B
  214018. Pure Appl. Chem.M
  214019. 17044N
  214020. 2/28/96
  214021. V+Iptycenes, cuppedophanes and cappedophanes.W
  214022. 1993X
  214023. 27-34Y
  214024. GABRIEL WEATHERHEAD
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  214029. -LACTAMS /ZnM
  214030. 17045N
  214031. 2/28/96V8The Ester Enolate-Imine Condensation Route to 
  214032. -Lactams.W
  214033. 1989X
  214034. 1447Y
  214035. GABRIEL WEATHERHEAD
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  214038. Chem. Rev.C/C-C BOND F RMATION /APPENDAGES /ENOLATES /ENOLSM
  214039. 17046N
  214040. 2/28/96V
  214041. Simple Enols.W
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  214043. GABRIEL WEATHERHEAD
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  214047. 17047N
  214048. 2/28/96VQThe gamma-Alkylation and gamma-Arylation of Dianons of beta-Dicarbonyl Compounds.W
  214049. 1969X
  214050. GABRIEL WEATHERHEAD
  214051. 16039
  214052. Hassner, A.//Fischer, B.B
  214053. HeterocyclesM
  214054. 17048N
  214055. 2/28/96V
  214056. New chemistry of oxazoles.W
  214057. 1441-65Y
  214058. GABRIEL WEATHERHEAD
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  214061. Acc. Chem. Res.C0FUNCTIONAL GROUPS /PREPARATIONS /AZIDES /C-X /N3M
  214062. 17049N
  214063. 2/28/96VXRegi specific and Stereospecific Introduction of Azide Functions into Organic Molecules.W
  214064. 1971X
  214065. GABRIEL WEATHERHEAD
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  214067. Hasserck, K.//Martin, H. D.B    SynthesisC
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  214069. 17050N
  214070. 2/28/96V[Synthesis of Seven-Membered Heterocycles via Pericyclic Reactions and Cyclic Intermediates.W
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  214072. GABRIEL WEATHERHEAD
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  214078. 2/28/96V-Consequences of Strain in (CH)8 Hydrocarbons.W
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  214080. 1125Y
  214081. GABRIEL WEATHERHEAD
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  214084. Org. React. (N.Y.)M
  214085. 17052N
  214086. 2/28/96V7The Baeyer-Villiger Oxidation of Aldehydes and Ketones.W
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  214088. GABRIEL WEATHERHEAD
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  214092. 17053N
  214093. 2/28/96V[Recent Developments in Methods for the Ester fication and Protection of the Carboxyl Group.W
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  214096. GABRIEL WEATHERHEAD
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  214099. 17054N
  214100. 2/28/96V.Metal Ammonia Reduction of Aromatic Compounds.W
  214101. 1970X
  214102. GABRIEL WEATHERHEAD
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  214105. TetrahedronC
  214106. FUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDE /C-X /OH /ALKOHOLS /TIN HYDRIDE /R3SnH /RADICAL  DEOXYGENATION /REDUCTION /ALKANES /SnM
  214107. 17055N
  214108. 2/28/96V9Modern Methods for the Radical Deoxygenation of Alcohols.W
  214109. 1983X
  214110. 2609Y
  214111. GABRIEL WEATHERHEAD
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  214115. 17056N
  214116. 2/28/96VHHydrogenolysis of Benzyl Groups Attached to Oxygen, Nitrogen, or Sulfur.W
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  214118. GABRIEL WEATHERHEAD
  214119. 16048
  214120. %A    Hazai, L.B
  214121. Adv. Heterocycl. Chem.M
  214122. 17057N
  214123. 2/28/96V43(2H)-Isoquinolones and their saturated derivatives.W
  214124. 1991X
  214125. GABRIEL WEATHERHEAD
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  214128. Chem. Rev.CZPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS /C+  /CYCLOPROPANESM
  214129. 17058N
  214130. 2/28/96VHLong Range Interact on of Cyclopropyl Groups with Carbonium Ion Centres.W
  214131. 1974X
  214132. GABRIEL WEATHERHEAD
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  214134. 'A Hayashi, T.//Kubo, A.//Ozawa, F.B
  214135. Pure Appl. Chem.M
  214136. 17059N
  214137. 2/28/96V*Catalytic asymmetric arylation of olefins.W
  214138. 1992X
  214139. GABRIEL WEATHERHEAD
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  214142. Pure Appl. Chem.C
  214143. 17060N
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  214146. 1992X
  214147. 1911-16Y
  214148. GABRIEL WEATHERHEAD
  214149. 16052
  214150. Hayashi, TM
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  214152. 2/28/96a
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  214154. 16053
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  214156. Acc. Chem. Res.M
  214157. 17062N
  214158. 2/28/96VKOsmylstion  f C60: Proof and characterization of the soccer-ball framework.W
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  214160. GABRIEL WEATHERHEAD
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  214165. 2/28/96V
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  214168. GABRIEL WEATHERHEAD
  214169. 16055
  214170. ,A*Hauser, C. R.//Swamer, F. W.//Adams, J. T.B
  214171. Org. React. (N.Y.)M
  214172. 17064N
  214173. 2/28/96VAThe Acylation of Ketones to Form 
  214174. -Diketones or 
  214175. -Keto Aldehydes.W
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  214177. GABRIEL WEATHERHEAD
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  214180. Org. React. (N.Y.)M
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  214184. GABRIEL WEATHERHEAD
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  214189. 17066N
  214190. 2/28/96VcAsymmetric Reductions with Chiral Complex Aluminium Hydrides and Tricoordinate Aluminium  Reagents.W
  214191. 1983X
  214192. GABRIEL WEATHERHEAD
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  214195. 17067N
  214196. 2/28/96V
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  214198. 1992X
  214199. GABRIEL WEATHERHEAD
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  214202. SynlettC
  214203. Si /PdM
  214204. 17068N
  214205. 2/28/96VxHighly selective cross-coupling reactions of organosilicon compounds mediated by fluoride ion and  a palladium cata yst.W
  214206. 1991X
  214207. GABRIEL WEATHERHEAD
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  214210. Org. R act. (N.Y.)
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  214212. 17069N
  214213. 2/28/96V2Palladium-Catalysed Vinylation of Organic Halides.W
  214214. 1982X
  214215. GABRIEL WEATHERHEAD
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  214220. 17070N
  214221. 2/28/96VWTransition metal-catalysed reaction of organic halides with CO, olefins and acetylenes.W
  214222. 1977X
  214223. GABRIEL WEATHERHEAD
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  214226. Pure Appl. Chem.M
  214227. 17071N
  214228. 2/28/96VnMechanistic investigations of a biomimetic polycyclization process that leads to the Daphniphyllum  alkaloids.W
  214229. 1990X
  214230. 1911Y
  214231. GABRIEL WEATHERHEAD
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  214233. Heathcock, C. H.B
  214234. Aldrichimica ActaCnC-C BOND FORMATION /APPENDAGES /DIASTEREOGENIC REACTIONS /1,2-ADDITION /OXAZOLIDINONE /CHIRAL AUXILIARY /ALDOLM
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  214236. 2/28/96VbUnderstanding and controlling diastereofacial selectivity in carbon-carbon bond-forming reactions.W
  214237. 1990X
  214238. GABRIEL WEATHERHEAD
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  214241. Top. Curr. Chem.M
  214242. 17073N
  214243. 2/28/96V>Novel organic peroxygen reagents for use in organic synthesis.W
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  214245. GABRIEL WEATHERHEAD
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  214247. Heaney, H.B
  214248. Aldrichimica ActaM
  214249. 17074N
  214250. 2/28/96VPOxidation reactions using magnesium monoperphthalate and urea hydrogen peroxide.W
  214251. 1993X
  214252. 35-45Y
  214253. GABRIEL WEATHERHEAD
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  214255. Heaney, H.B Organometallic Chemistry ReviewsC+ORG NOMETALLICS /LITHIUM /MAGNESIUM /Li /MgM
  214256. 17075N
  214257. 2/28/96VPGrignard and Organolithium Reagents Derived from Di- and Poly-halogen Compounds.W
  214258. 1965X
  214259. GABRIEL WEATHERHEAD
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  214261. Heinisch, G.B
  214262. Hete ocyclesC
  214263. C-C BOND FORMATION /HETEROANNULATIONS /ALPHA-ALKOXYALKYLATION  /ALPHA-N-AMIDOALKYLATION /ACYLATION /ALKOXYCARBONYLATION /PYRIDAZINESM
  214264. 17076N
  214265. 2/28/96
  214266. Advances in the Synthesis of Substituted Pyridazines via Introduction of Carbon Functional Groups  into the Parent Heterocycle.W
  214267. 1987X
  214268. GABRIEL WEATHERHEAD
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  214270. 9A#Heinekey, D. M.//Oldham, W. J., Jr.B
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  214272. 17077N
  214273. 2/28/96V%Coordination chemistry of dihydrogen.W
  214274. 1993X
  214275. 913-26Y
  214276. GABRIEL WEATHERHEAD
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  214279. Angew. Chem., Int. Ed. Engl.M
  214280. 17078N
  214281. 2/28/96Vr3-Amino-2H-azirine. Synthons for alpha,alpha- isubstituted alpha-amino acids in heterocycle and peptide synthesis.W
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  214283. GABRIEL WEATHERHEAD
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  214286. Adv. Photochem.M
  214287. 17079N
  214288. 2/28/96VJThe decomposition of alkyl nitrites and the reactions of alkoxyl radicals.W
  214289. 1988X
  214290. GABRIEL WEATHERHEAD
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  214293. J. Organomet. Chem.C
  214294. 17080N
  214295. 2/28/96VNTransition-Metals In Organic-Synthesis - Annual Survey Covering The  Year 1992W
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  214298. GABRIEL WEATHERHEAD
  214299. 16072
  214300. Hegedus, L. S.B
  214301. Pure Appl. Chem.C
  214302. ORGANOMETALLICS /CHROMIUM /CrM
  214303. 17081N
  214304. 2/28/96VPChromium carbene complexes in the synthesis of molecules of biological interest.W
  214305. 1990X
  214306. GABRIEL WEATHERHEAD
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  214308. Hegedus, L. J.B
  214309. Angew. Chem., Int. Ed. Engl.CcC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /ORGANOMETALLICS /PALLADIUM  /INDOLES /Pd /TMM
  214310. 17082N
  214311. 2/28/96VDTransition Metals in the Synthesis and Functionalisation of Indoles.W
  214312. 1988X
  214313. 1113Y
  214314. GABRIEL WEATHERHEAD
  214315. 16074
  214316. Hegedus, L. S.B
  214317. TetrahedronC
  214318. ORGANOMETALLICS /PALLADIUM /PdM
  214319. 17083N
  214320. 2/28/96V1Palladium (II)-assisted Reactions of Monoolefins.W
  214321. 1984X
  214322. 2415Y
  214323. GABRIEL WEATHERHEAD
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  214325. Henne, A. L.B
  214326. Org. React. (N.Y.)C
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  214328. 2/28/96V0The Preparation of Aliphatic Fluorine Compounds.W
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  214330. GABRIEL WEATHERHEAD
  214331. 16076
  214332. AA1Hendrickson, J. B.//Sternbach, D. D.//Baer, K. W.B
  214333. Acc. Chem. Res.
  214334. FUNCTIONAL GROUPS /TRANSFORMATIONS /C-X TO C-Y /Tf2O /TRIFLIC ANHYDRIDE  /N-TRIFYLIMIDAZOLE /PhNTf2 /PHENYLTRIFLIMIDE /TRIFLONES /C-X /SO2CF3 /TRIFLAMIDES  /R2NTf /TRIFLATES /C-X /OTfM
  214335. 17085N
  214336. 2/28/96V'Trifyl Acti ation in Organic Synthesis.W
  214337. 1977X
  214338. GABRIEL WEATHERHEAD
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  214340. Hendrickson, J. B.B
  214341. Angew. Chem., Int. Ed. Engl.C,PHYSICAL ORGANIC /REARRANGEMENTS /PERICYCLICM
  214342. 17086N
  214343. 2/28/96V,The Variety of Thermal Pericyclic Reactions.W
  214344. 1974X
  214345. GABRIEL WEATHERHEAD
  214346. 16078
  214347. Henderson, J. W.B
  214348. Chem. Soc. Rev.CFPHYSICAL ORGANIC /STEREOCHEMISTRY /CARBOCATIONS /CARBOANIONS /RADICALSM
  214349. 17087N
  214350. 2/28/96V6Chirality in Carbonium Ions, Carbanions, and Radicals.W
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  214352. GABRIEL WEATHERHEAD
  214353. 16079
  214354. Hewitt, D.B
  214355. Adv. Heterocycl. Chem.C
  214356. HETEROCYCLES /PM
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  214358. 2/28/96V The chemistry of azaphosphorins.W
  214359. 1988X
  214360. GABRIEL WEATHERHEAD
  214361. 16080
  214362. Hessen, B.//Teuben, J. H.B
  214363. J. Organomet. Chem.
  214364. EC9ORGANOMETALLICS /TITANIUM /ZIRCONIUM /HAFNIUM /Ti /Zr /HfM
  214365. 17089N
  214366. 2/28/96VMProperties of electron defficient 1,3-diene complexes of the group 4A metals.W
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  214368. GABRIEL WEATHERHEAD
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  214372. 17090N
  214373. 2/28/96VuWater-soluble ligands, metal complexes, and complex catalysts: synergism of homogeneous and  heterogeneous catalysis.W
  214374. 1993X
  214375. 1524-44Y
  214376. GABRIEL WEATHERHEAD
  214377. 16082
  214378. GA3Herndon, J. W.//Wu, C.//Horp, J. J.//Krauzer, K. A.B
  214379. SynlettC
  214380. Sn /FeM
  214381. 17091N
  214382. 2/28/96VwExploration of the [3+2] Cycloaddition Reaction Between Allylstannanes and alpha,  beta-Unsaturated Acyliron Complexes.W
  214383. 1991X
  214384. GABRIEL WEATHERHEAD
  214385. 16083
  214386. HA0Hermez, I.//Kereszturi, G.//Vasvari-Debreczy, L.B
  214387. Adv. Heterocycl. Chem.M
  214388. 17092N
  214389. 2/28/96V@Aminomethylenemalonates and their use in heterocyclic synthesis.W
  214390. 1992X
  214391. GABRIEL WEATHERHEAD
  214392. 16084
  214393. Hermecz, I.B
  214394. Adv. Heterocycl. Chem.
  214395. IC8REAGENTS /SOLVENTS /CATALYSTS /DBU /DIAZABICYCLOUNDECENEM
  214396. 17093N
  214397. 2/28/96VCChemistry of Diazabicycloundecene (DBU) and Other Pyrimidoazepines.W
  214398. 1987X
  214399. GABRIEL WEATHERHEAD
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  214401. Herge , R.B
  214402. Angew. Chem., Int. Ed. Engl.M
  214403. 17094N
  214404. 2/28/96VTOrganizing principle of complex reactions and theory of coarctate transition states.W
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  214407. GABRIEL WEATHERHEAD
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  214410. Adv. Heterocycl. Chem.M
  214411. 17095N
  214412. 2/28/96V$Advances in tetramic acid chemistry.W
  214413. 1993X
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  214415. GABRIEL WEATHERHEAD
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  214417. Hill, E. A.B
  214418. Adv. Organomet. Chem.C/ORGANOMETALLICS /MAGNESIUM /CARBOMETALATION /MgM
  214419. 17096N
  214420. 2/28/96V
  214421. Organomagnesium Rearrangements.W
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  214423. GABRIEL WEATHERHEAD
  214424. 16088
  214425. MA    Hideg, K.B
  214426. Pure Appl. Chem.M
  214427. 17097N
  214428. 2/28/96V.Novel, potentially useful spin-label reagents.W
  214429. 1990X
  214430. GABRIEL WEATHERHEAD
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  214435. 2/28/96V
  214436. Towards Novel Organic-Synthesis On Multimetallic Centers - Syntheses  And Reactivities Of  Dinuclear Ruth nium Thiolate ComplexesW
  214437. 1994X
  214438. 1-14Y
  214439. GABRIEL WEATHERHEAD
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  214441. Hibbert, F.//Emsley, J.B
  214442. Adv. Phys. Org. Chem.C
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  214444. 17099N
  214445. 2/28/96V)Hydrogen bonding and chemical reactivity.W
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  214447. GABRIEL WEATHERHEAD
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  214449. Hibbert, F. H.B
  214450. Acc. Chem. Res.CCPHYSICAL ORGANIC /MECHANISMS /ACIDS /DEPROTONATION /PROTON TRANSFERM
  214451. 17100N
  214452. 2/28/96V<Proton Transfer from Intramolecularly Hydrogen-Bonded Acids.W
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  214454. GABRIEL WEATHERHEAD
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  214456. Heyhawkins, E.B
  214457. Chem. Rev.C
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  214459. 17101N
  214460. 2/28/96V
  214461. Bis(cyclopentadienyl)zirconium(iv) Or Hafnium(iv) Compounds With Si-,  Ge-, Sn-, N-, P-,  As-, Sb-, O-, S-, Se-, Te-, Or Transition  Metal-Centered Anionic LigandsW
  214462. 1994X    1661-1717Y
  214463. GABRIEL WEATHERHEAD
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  214465. RA;Hewlins, M. J. E.//Olveira-Campos, A.-M.//Shannon, P. V. R.B    SynthesisC
  214466. TARGET SYNTHESIS /MISCELLANEOUSM
  214467. 17102N
  214468. 2/28/96VgSynthetic Approaches to Ellipticines and Other Derivatives and Analogues of  6H-Pyrido[4,3-6]carbazole.W
  214469. 1984X
  214470. GABRIEL WEATHERHEAD
  214471. 16094
  214472. Hewitt, C. D.//Silvester, M. J.B
  214473. Aldrichimica ActaC    ARENES /FM
  214474. 17103N
  214475. 2/28/96VKFluoroaromatic compounds: synthesis, reactions and commercial applications.W
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  214477. GABRIEL WEATHERHEAD
  214478. 16095
  214479. TA    Hirst, J.B%Journal of Physical Organic ChemistryM
  214480. 17104N
  214481. 2/28/96VmMechanisms of aromatic nucleophilic su stitution reactions by amines in solvents of low relative permitivity.W
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  214483. 68-79Y
  214484. GABRIEL WEATHERHEAD
  214485. 16096
  214486. Hirsch, A.B
  214487. Angew. Chem., Int. Ed. Engl.M
  214488. 17105N
  214489. 2/28/96V-The chemistry of the fullerenes: an overview.W
  214490. 1993X
  214491. 1138-41Y
  214492. GABRIEL WEATHERHEAD
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  214494. Hirsch, J. A.B
  214495. Top. Stereochem.C/PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATIONM
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  214497. 2/28/96V!Table of Conformational Energies.W
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  214499. GABRIEL WEATHERHEAD
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  214501. Hirama, M.//Ito, S.B
  214502. HeterocyclesC
  214503. C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /1,4-ADDITION /ENOATES  /HETEROANNULATION /6(O) /INTRAMOLECULAR /CARBOHYDRATES /AMINO SUGARSM
  214504. 17107N
  214505. 2/28/96V
  214506. Asymmetric Induction in the Intramolecular Conjugate Addition of gamma- or  delta-Carbamoyloxy-alpha, beta-Unsaturated Esters. Diastereoselective Amination and Divergent  Syntheses of 3-Amino-2,3,6-Dideoxyhexoses.W
  214507. 1989X
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  214509. GABRIEL WEATHERHEAD
  214510. 16099
  214511. Hilvert, D.B
  214512. Acc. Chem. Res.M
  214513. 17108N
  214514. 2/28/96V@Antibody catalysis of carbon-carbon bond formation and cleavage.W
  214515. 1993X
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  214517. GABRIEL WEATHERHEAD
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  214519. Hill, A. F.B
  214520. Adv. Organomet. Chem.C
  214521. 17109N
  214522. 2/28/96V>Organotransition metallic chemistry of sulfur dioxide analogs.W
  214523. 1994X
  214524. GABRIEL WEATHERHEAD
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  214526. ZA7Hill, L.//Richards, C. J.//Saberi, S. P.//Thomas, S. E.
  214527. Pure Appl. Chem.C
  214528. 17110N
  214529. 2/28/96VjSynthes s and reactivity of iron tricarbonyl complexes of vinylketenes, vinylketenimines and vinylallenes.W
  214530. 1992X
  214531. GABRIEL WEATHERHEAD
  214532. 16102
  214533. Hoffman, R. V.B
  214534. TetrahedronC
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  214536. 17111N
  214537. 2/28/96ViSynthetic transformations using arenesulfonyloxy groups, first as electrophiles, then as leaving  groups.W
  214538. 1991X
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  214540. GABRIEL WEATHERHEAD
  214541. 16103
  214542. \A'Hoffman, R. V.//Bartsch, R.//Cho, B. R.B
  214543. Acc. Chem. Res.C
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  214545. 17112N
  214546. 2/28/96V7Base-promoted, imine-forming 1,2-elimination rea tions.W
  214547. 1989X
  214548. GABRIEL WEATHERHEAD
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  214550. Hoff ann, R. W.B
  214551. Angew. Chem., Int. Ed. Engl.M
  214552. 17113N
  214553. 2/28/96V;Flexible molecules with definite shape-conformation design.W
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  214556. GABRIEL WEATHERHEAD
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  214559. Top. Stereochem.C4PHYSICAL ORGANIC /STEREOCHEMISTRY /CONFORMATION /NMRM
  214560. 17114N
  214561. 2/28/96VPThe Lanthanide Induced Shift Technique: Applications in Conformational Analysis.W
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  214563. GABRIEL WEATHERHEAD
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  214566. Angew. Chem., Int. Ed. Engl.C>PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /CARBENESM
  214567. 17115N
  214568. 2/28/96V3Generation of Carbenes by Thermal Cycloelimination.W
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  214570. GABRIEL WEATHERHEAD
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  214573. Top. Curr. Chem.M
  214574. 17116N
  214575. 2/28/96VCThrough-bond modulation of reaction centers by remote substituents.W
  214576. 1990X
  214577. GABRIEL WEATHERHEAD
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  214580. TetrahedronC5ORGANOMETALLICS /GENERAL /C-M /HSAB /CHEMOSELECTIVITYM
  214581. 17117N
  214582. 2/28/96V?Chemoselectivity of Organometallic Reactions. A HSAB Appraisal.W
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  214584. GABRIEL WEATHERHEAD
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  214586. bA    Ho, T.-L.B    SynthesisCTORGANOMETALLICS /CHROMIUM /MOLYBDENUM /TUNGSTEN /TITANIUM /REDUCTION /Cr /Mo /W  /Ti
  214587. 17118N
  214588. 2/28/96VXReduction of Organic Compounds with Low-V lent Species of Group IVB, VB, and VIB Metals.W
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  214590. GABRIEL WEATHERHEAD
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  214592. cA    Ho, T. L.B    SynthesisC9FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUS /REAGENTS /CeM
  214593. 17119N
  214594. 2/28/96V)Ceric Ion Oxidation in Organic Chemistry.W
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  214596. GABRIEL WEATHERHEAD
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  214598. dA    Ho, T.-L.B"Research on Chemical IntermediatesC$PHYSICAL ORGANIC /CONTRAPOLARIZATIONM
  214599. 17120N
  214600. 2/28/96V8Contrapolarization, a new concept in organic reactivity.W
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  214602. GABRIEL WEATHERHEAD
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  214606. 17121N
  214607. 2/28/96V5The Di- -methane and Oxa-di- -methane Rearrangements.W
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  214609. GABRIEL WEATHERHEAD
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  214613. 17122N
  214614. 2/28/96VLThe stereochemistry of nucleophilic substitution of tetracoordinate silicon.W
  214615. GABRIEL WEATHERHEAD
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  214618. Adv. Phys. Org. Chem.C4PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBANIONSM
  214619. 17123N
  214620. 2/28/96V+Ion-Pairing Effects in Carbanion Reactions.W
  214621. 1977X
  214622. GABRIEL WEATHERHEAD
  214623. 16115
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  214626. 17124N
  214627. 2/28/96V3Enantioselective epoxidation with peroxidic oxygen.W
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  214629. GABRIEL WEATHERHEAD
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  214632. Angew. Chem., Int. Ed. Engl.C2REAGENTS /DMAP /4-DIMETHYLANINOPYRIDINE /ACYLATIONM
  214633. 17125N
  214634. 2/28/96VB4-Dimethylaninopyridine (DMAP) as a Highly Active Acylation Agent.W
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  214636. GABRIEL WEATHERHEAD
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  214638. Hoffmann, H. M. R.B
  214639. Angew. Chem., Int. Ed. Engl.M
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  214650. 2/28/96
  214651. kVNAllylic 1,3-strain as a controlling factor in stereoselective transformations.W
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  214657. Pure Appl. Chem.C
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  214660. 2/28/96V?alpha-Chiral Allylboronates: Reagents for Asymmetric Synthesis.W
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  214662. GABRIEL WEATHERHEAD
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  214668. Stereoselective Syntheses Of Building-Blocks With 3 Consecutive Stereogenic Centers - Important  Precursors Of Polyketide Natural-ProductsW
  214669. 1987X
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  214671. GABRIEL WEATHERHEAD
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  214674. Angew. Chem., Int. Ed. Engl.
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  214676. 17130N
  214677. 2/28/96VoThe Cycloaddition of Allyl Cations to 1,3-Dienes: General Methods for the Synthesis of 7-Membered  Carbocycles.W
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  214679. GABRIEL WEATHERHEAD
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  214684. 17131N
  214685. 2/28/96V>Diastereogenic Addition of Crotylmetal Compounds to Aldehydes.W
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  214690. Angew. Chem., Int. Ed. Engl.C<C-C BOND FORMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[2,3]M
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  214692. 2/28/96V4Stereochemistry of [2,3]-Sigmatropic Rearrangements.W
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  214694. GABRIEL WEATHERHEAD
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  214699. 17133N
  214700. 2/28/96V>Syntheses of Seven and Five-Membered Rings from Allyl Cations.W
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  214702. GABRIEL WEATHERHEAD
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  214705. Acc. Chem. Res.C#PHYSICAL ORGANIC /STEREOELECTRONICSM
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  214707. 2/28/96V8Interaction of Orbitals Through Space and Through Bonds.W
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  214709. GABRIEL WEATHERHEAD
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  214712. Angew. Chem., Int. Ed. Engl.C6C-C BOND FORMATION /PERICYCLIC REACTIONS /ENE REACTIONM
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  214714. 2/28/96V
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  214720. Pure Appl. Chem.CRC-C BOND FORMATION /APPENDAGES /1,2-ADDITION /ALKYLATION /DIASTEREOGENIC REACTIONS
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  214722. 2/28/96VUMetalated 2-alkenyl carbamates: chiral homoenolate reagents for asymmetric synthesis.W
  214723. 1990X
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  214725. GABRIEL WEATHERHEAD
  214726. 16128
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  214728. Angew. Chem., Int. Ed. Engl.C
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  214730. 17137N
  214731. 2/28/96VTThe Homoaldol Reaction, or How to Overcome Problems of Regio- and Stereoselectivity.W
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  214733. GABRIEL WEATHERHEAD
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  214735. vA    Hoppe, D.B
  214736. Angew. Chem., Int. Ed. Engl.C8C-C BOND FORMATION /APPENDAGES /ENOLATES /C-M(X) /L (NC)M
  214737. 17138N
  214738. 2/28/96V1alpha-Metalated Isocyanides in Organic Synthesis.W
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  214740. GABRIEL WEATHERHEAD
  214741. 16130
  214742. Hopf, H.//Witulski, B.B
  214743. Pure Appl. Chem.M
  214744. 17139N
  214745. 2/28/96VJCyanoalkynes: magic wands for the preparation of novel aromatic compounds.W
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  214748. GABRIEL WEATHERHEAD
  214749. 16131
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  214751. Nat. Prod. Rep.
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  214753. 17140N
  214754. 2/28/96VuRecent Developments in the Birch Reduction of Aromatic Compounds: Applications to the Synthesis  of Natural Products.W
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  214759. Angew. Chem., Int. Ed. Engl.C7PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICAL ANIONM
  214760. 17141N
  214761. 2/28/96V1Radical Anion Intermediates in Organic Chemistry.W
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  214763. GABRIEL WEATHERHEAD
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  214772. GABRIEL WEATHERHEAD
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  214775. A c. Chem. Res.C
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  214781. GABRIEL WEATHERHEAD
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  214786. 2/28/96
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  214789. GABRIEL WEATHERHEAD
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  214794. 2/28/96VZMagnesium Compounds - Classification And Analysis Of Crystallographic  And Structural DataW
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  214801. Pure Appl. Chem.C
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  214803. 2/28/96V<Thiacrown compounds with 1,2-dicyano-1,2-dithioethene units.W
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  214810. 17147N
  214811. 2/28/96VzIs the transition state indeed intermediate between  eactants and products? The Michael addition reaction as a case study.W
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  214818. 2/28/96V.Trifluoromethanesulfonic Acid and Derivatives.W
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  214820. GABRIEL WEATHERHEAD
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  214825. 2/28/96V(Substrate-directable chemical reactions.W
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  214840. 2/28/96VAQuantitative modeling of proximity effects on organic reactivity.W
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  214855. 17153N
  214856. 2/28/96VlCharacteristics in the Reactions of Allyl Sila es and Their Applications to Versatile Synthetic Equivalents.W
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  214858. GABRIEL WEATHERHEAD
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  214863. 2/28/96VJSynthesis of oxygen-containing heterocycles using palladium(II) catalysts.W
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  214870. 17155N
  214871. 2/28/96V)New aspects of oxypalladation of alkenes.W
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  214878. 2/28/96VMSyntheses, structures, bonding and reactivity of main group heterocarboranes.W
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  214885. 2/28/96VxEnzymic hydroxylation of arene and symmetry considerations in efficient synthetic design of oxygenated natural products.W
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  214900. 17159N
  214901. 2/28/96V:Anionic Approaches to the Construction of Cyclopentanoids.W
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  214907. Org. React. (N.Y.)CaREAGENTS /DIETHYLAMINOSULFUR TRIFLUORIDE /AMINOFLUOROSULFURANES /FLUORINATION  /C-X /F /FLUORIDESM
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  214909. 2/28/96VSFluorination with Diethylaminosulfur Trifluorid  and Related Aminofluorosulfuranes.W
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  214911. GABRIEL WEATHERHEAD
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  214914. Org. React. (N.Y.)CUC-C BOND FORMATION /ANNULATIONS /5-RING /EXPANSION /PHYSICAL ORGANIC  /REARRANGEMENTSM
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  214931. Heterocyclic ketene aminals.W
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  214939. 2/28/96VQPerfluoroalkylation initiated with sodium dithionite and related reagent systems.W
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  214941. GABRIEL WEATHERHEAD
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  214945. 2/28/96VDSynthetic applications of organoantimony compounds.  Acc. Chem. Res.W
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  214952. 2/28/96V;Arene-arene interactions: electrostatic or charge-transfer?W
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  214958. Org. Prep. Pr ced. Int.C0C-C BOND FORMATION /APPENDAGES /1,4-ADDITION /LiM
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  214960. 2/28/96V6Michael addition of organolithium compounds. A review.W
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  214975. 2/28/96V;Enantioselectivity of some lipases: control and prediction.W
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  214991. 2/28/96V8Electrocyclic Ring Opening Reactions of Ethylene Oxides.W
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  214998. 2/28/96V@Cycloadditions-Definition, Classification, and Characterisation.W
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  215005. 2/28/96V(Progress in the Fischer indole reaction.W
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  215022. 2/28/96VDO gano-transition metal compounds containing perfluorinated ligands.W
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  215028. 2/28/96V4Metal-Ammonia Reduction of Cyclic Aliphatic Ketones.W
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  215035. 2/28/96V7Aromatic /quinoid systems: principles and applications.W
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  215042. 2/28/96VkAn Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4+1]Azide-Diene Annulation  Methodology.W
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  215049. 2/28/96VmSynthesis and reactions of lithiated monocyclic azoles containing two or more heteroatoms. Part II: Oxazoles.W
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  215056. 17180N
  215057. 2/28/96
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  215066. 2/28/96V?Metallation and Metal-Halogen Exchange Reactions of Imidazoles.W
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  215068. GABRIEL WEATHERHEAD
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  215071. Pure Appl. Chem.M
  215072. 17182N
  215073. 2/28/96VLApplication of ESE spectroscopy to the st dy of radical reactions in solids.W
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  215080. 2/28/96V[New aspects of organocopper reagents: 1,3- and 1,2-chiral induction and reaction mechanism.W
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  215091. GABRIEL WEATHERHEAD
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  215097. V,Counterat ack Reagents in Organic Reactions.W
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  215100. GABRIEL WEATHERHEAD
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  215104. 17186N
  215105. 2/28/96VBSteric Influence of the Trimethylsilyl Group in Organic Reactions.W
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  215112. 2/28/96V5Recent Advances in Halogenation of Organic Compounds.W
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  215114. GABRIEL WEATHERHEAD
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  215120. 2/28/96V=Camptothecin: Chemistry, Biogenesis, and Medicinal Chemistry.W
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  215123. GABRIEL WEATHERHEAD
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  215127. 2/28/96VWMeerwein-Ponndorf-Verley Reductions And Oppenauer Oxidations - An  Integrated Approach.W
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  215134. 2/28/96V!AIDS-driven nucleoside chemistry.W
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  215140. Adv. Heterocycl. Chem.M
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  215142. 2/28/96V1The nitration of phenyl-substituted heterocycles.W
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  215145. GABRIEL WEATHERHEAD
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  215150. 2/28/96V;The role of aromatic interactions in molecular recognition.W
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  215156. Acc. Chem. Res.M
  215157. 17193N
  215158. 2/28/96VxThe unusual and the unexpected in an old reac ion. The photochlorination of alkanes with molecular chlorine in solution.W
  215159. 1990X
  215160. GABRIEL WEATHERHEAD
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  215163. Org. React. (N.Y.)M
  215164. 17194N
  215165. 2/28/96V
  215166. The Resolution of Alcohols.W
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  215168. GABRIEL WEATHERHEAD
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  215170. Inch, T. D.B
  215171. TetrahedronCIFUNCTIONAL GROUPS /TRANSFORMATIONS /CARBOHYDRATES /CHIRONS /CARBOHYDRATESM
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  215173. 2/28/96
  215174. V[Formation of Convenient Chiral Intermediates from Carbohydrates and their Use in Synthesis.W
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  215177. GABRIEL WEATHERHEAD
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  215180. Pure Appl. Chem.C
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  215182. 17196N
  215183. 2/28/96V1Synthesis and reactions of new phosphine-boranes.W
  215184. 1993X
  215185. 655-60Y
  215186. GABRIEL WEATHERHEAD
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  215189. Pure Appl. Chem.C$ORGANOMETALLICS /ELEMENT /CERIUM /CeM
  215190. 17197N
  215191. 2/28/96V8Carbonyl addition reactions promoted by cerium reagents.W
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  215193. GABRIEL WEATHERHEAD
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  215196. Acc. Chem. Res.C:C-C BOND FORMATION /ANNULATIONS /MEDIUM RING /RING C OSUREM
  215197. 17198N
  215198. 2/28/96V7Ring Closure Reactions of Bifunctional Chain Molecules.W
  215199. 1981X
  215200. GABRIEL WEATHERHEAD
  215201. 16190
  215202. A"Ikeda, M.//Sato, T.//Ishibashi, H.B
  215203. HeterocyclesC
  215204. HETEROCYCLESM
  215205. 17199N
  215206. 2/28/96V3Recent advances in the synthesis of pyrrolizidines.W
  215207. 1988X
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  215209. GABRIEL WEATHERHEAD
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  215211. Ihara, M.//Fukumoto, K.
  215212. Angew. Chem., Int. Ed. Engl.M
  215213. 17200N
  215214. 2/28/96V^Syntheses of polycyclic natural products employing the intramolecular double Michael reaction.W
  215215. 1993X
  215216. 1010-22Y
  215217. GABRIEL WEATHERHEAD
  215218. 16192
  215219. Ide, W. S.//Buck, J. S.B
  215220. Org. React. (N.Y.)M
  215221. 17201N
  215222. 2/28/96V
  215223. The Synthesis of Benzoins.W
  215224. 1948X
  215225. GABRIEL WEATHERHEAD
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  215228. HeterocyclesM
  215229. 17202N
  215230. 2/28/96ViSynthesis And Reactions Of Lithiated Monocyclic Azoles Containing 2 Or  More Hetero-Atoms .4.  ImidazolesW
  215231. 1994X    2487-2568Y
  215232. GABRIEL WEATHERHEAD
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  215234. Ireland, J  E.//Wyatt, P. A. H.B
  215235. Adv. Phys. Org. Chem.CKFUNCTIONAL GROUPS /TRANSFORMATIONS /PHOTOCHEMICAL REACTIONS /PHOTOCHEMISTRYM
  215236. 17203N
  215237. 2/28/96VKAcid Base Properties of Electronically Excited States of Organic Molecules.W
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  215239. GABRIEL WEATHERHEAD
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  215244. 2/28/96
  215245. VmTransition Metal-Promoted Free-Radical Reactions in Organic Synthesis: The Formation of  Carbon-Carbon Bonds.W
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  215248. GABRIEL WEATHERHEAD
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  215252. 17205N
  215253. 2/28/96V/Asymmetric photochemical reactions in solution.W
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  215255. GABRIEL WEATHERHEAD
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  215259. 17206N
  215260. 2/28/96V|Design concepts for developing highly efficient chiral bisphosphine ligands in rhodium-catalyzed  asymmetric hydrogenations.W
  215261. 1992X
  215262. GABRIEL WEATHERHEAD
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  215266. 17207N
  215267. 2/28/96VQThermodynamic and kinetic data for macrocycle interaction with neutral molecules.W
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  215270. GABRIEL WEATHERHEAD
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  215275. 2/28/96VSThermodynamic and kinetic data for macrocycle interactions with cations and anions.
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  215278. GABRIEL WEATHERHEAD
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  215281. Acc. Chem. Res.M
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  215283. 2/28/96V\Studies of organic di-, oligo-, and polyradicals by means of their bulk magnetic properties.W
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  215289. 17210N
  215290. 2/28/96V'Antitumor substances from higher plantsW
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  215297. 2/28/96V"Synthesis of bioactive sialosides.W
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  215305. 2/28/96VIRecent progress in the synthesis of butenolide carotenoids and retinoids.W
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  215310. 17213N
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  215316. Pure Appl. Chem.C
  215317. C-C BOND FORMATION /APPENDAGESM
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  215319. 2/28/96V9New metalation and synthetic applications of isonitriles.W
  215320. GABRIEL WEATHERHEAD
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  215325. 2/28/96V@Dendrimers - From Generations And Functional-Groups To FunctionsW
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  215332. 17216N
  215333. 2/28/96V6Methodolo ies for synthesis of heterocyclic compounds.W
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  215341. 2/28/96V
  215342. Methodology for stereochemical control in bioactive natural product synthesis-new methods toward  enediyne antitumor antibiotics.W
  215343. 1990X
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  215345. GABRIEL WEATHERHEAD
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  215347. Isaacs, N. S.B
  215348. TetrahedronCLODDS AND ENDS /TECHNIQUES AND METHODS /CYCLOADDITION /[4+2] /BAYLISS-HILLMANM
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  215350. 2/28/96V7The role of high-pressure methods in organic chemistry.W
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  215352. GABRIEL WEATHERHEAD
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  215358. Th  Synthesis of Acetylenes.W
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  215364. 2/28/96V0Small molecule, big potential (oxalyl chloride).W
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  215378. TetrahedronC7C-C BOND FORMATION /APPENDAGES /ENOLATES /C=C-X-M /O-LiM
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  215380. 2/28/96V2Structure and Reactivity of Alkali Metal Enolates.W
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  215388. 2/28/96V+Resolution of Enantiomers via Biocatalysis.W
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  215396. 2/28/96V[Modified Raney nickel catalyst: Heterogeneous enantiodifferentiating (asymmetric) catalyst.W
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  215401. Angew. Chem., Int. Ed. Engl.CPC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /REDUCTION /HYDROGENATIONM
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  215403. 2/28/96VJMethods of Asymmetric Synthesis. Enantioselective Catalytic Hydrogenation.W
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  215410. 2/28/96V*The Perkin Reaction and Related Reactions.W
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  215417. 2/28/96VQMetallaoxetanes as intermediate in oxygen-transfer reactions--reality or fiction?W
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  215433. 2/28/96VmMetallacyclobutane Complexes Of The Group-8 Transition-Metals -  Synthesis, Characterizations,  And  hemistryW
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  215440. 2/28/96VHThe photo-oxygenation of olefins and the role of zwitterionic peroxides.W
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  215447. 2/28/96V3Intramolecular coordination in organotin chemistry.W
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  215460. J. Fluorine Chem.C
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  215464. 1989X
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  215479. 2/28/96V^Bioorganometallic chemistry: a future direction for transition metal organometallic chemistry?W
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  215487. 2/28/96V*The synthesis of drimane sesquiterpenoids.W
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  215494. 2/28/96VxTandem Transformations Initiated By The Migration Of A Silyl Group -  Some New Synthetic  Applications Of Silyloxiranes.W
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  215502. 2/28/96VGBulky or supracyclopentadienyl derivatives in organometallic chemistry.W
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  215532. 2/28/96V*Photochemistry of radicals and biradicals.W
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  215548. 2/28/96V>Applications of enzymes in the synthesis of bioactive polyols.W
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  215556. 2/28/96VAFullerene structure and dynami s: A magnetic resonance potpourri.W
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  215570. Aldrichimica Acta
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  215573. 2/28/96V*Applications of Sulfoximines in Synthesis.W
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  215581. 2/28/96V6The Reactivity-Selectivity Principle: Fact or Fiction?W
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  215589. 2/28/96VNReactions of Electrophiles with sigma-Bonded Organotransition-Metal Complexes.W
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  215594. Angew. Chem., Int. Ed. Engl.C.C-C BOND FORMATION /ANNULATIONS /MIS ELLANEOUSM
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  215596. 2/28/96V Biomimetic Polyene Cyclisations.W
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  215601. Acc. Chem. Res.CFC-C BOND FORMATION /APPENDAGES /1,2-ADDITION /SULPHUR /SULFOXIMINES /SM
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  215619. 2/28/96V<The Formation of Cyclic Ketones by Intramolecular Acylation.W
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  215621. GABRIEL WEATHERHEAD
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  215625. PHYSICAL ORGANIC /TMM
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  215627. 2/28/96V^Comparative reactivities of hydrocarbon carbon-hydrogen bonds with a transition-metal complex.W
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  215629. GABRIEL WEATHERHEAD
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  215633. REAGENTS /BIOTRANSFORMATIONM
  215634. 17255N
  215635. 2/28/96V
  215636. Enzymes in Organic Synthesis.W
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  215645. V@Olefinic Microbial Metabolites, Excluding Macrocyclic Compounds.W
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  215647. GABRIEL WEATHERHEAD
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  215653. 2/28/96V6The Less Familiar Reactions of Organocadmium Reagents.W
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  215655. GABRIEL WEATHERHEAD
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  215663. GABRIEL WEATHERHEAD
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  215668. 2/28/96VHThe Halogen-Metal Interconversion Reaction with Organolithium Compounds.W
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  215670. GABRIEL WEATHERHEAD
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  215675. 2/28/96V@New findings in the arene chemistry of the 3d transition metals.W
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  215680. Acc. Chem. Res.
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  215683. 2/28/96VQConformational Analysis of Six-Membered Sulfur-Containing Saturated Heterocycles.W
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  215685. GABRIEL WEATHERHEAD
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  215691. 2/28/96V<Ninhydrin and ninhydrin analogs. Syntheses and applications.W
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  215699. 2/28/96V
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  215710. GABRIEL WEATHERHEAD
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  215723. 2/28/96VCTetrathiafulvalenes as building-blocks in supramolecular chemistry.W
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  215726. GABRIEL WEATHERHEAD
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  215730. 17267N
  215731. 2/28/96V(Transition-Metal-Catalysed Epoxidations.W
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  215733. GABRIEL WEATHERHEAD
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  215736. Acc. Chem. Res.C*PH SICAL ORGANIC /FREE ENERGY CALCULATIONSM
  215737. 17268N
  215738. 2/28/96VTFree energy calculations: a breakthrough for modeling organic chemistry in solution.W
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  215740. GABRIEL WEATHERHEAD
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  215751. Adv. Organomet. Chem.M
  215752. 17270N
  215753. 2/28/96VGChemistry of cationic dicyclopentadie yl group 4 metal-alkyl complexes.W
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  215755. GABRIEL WEATHERHEAD
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  215760. 17271N
  215761. 2/28/96VFCationic zirconium catalysts for carbon carbon bond forming chemistry.W
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  215763. GABRIEL WEATHERHEAD
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  215776. 2/28/96V-Main-group metallocenes: Recent developments.W
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  215785. 2/28/96V! -Bonding in Main Group Elements.W
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  215801. 2/28/96VU(R)- and (S)-2,3-O-Isopropylideneglyceraldehyde in Stereoselective Organic Synthesis.W
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  215803. GABRIEL WEATHERHEAD
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  215808. 17277N
  215809. 2/28/96VYalpha-Oxoketene-S,S-, N,S- and N,N-acetals: versatile intermediates in organic synthesis.W
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  215817. 2/28/96VGDesign Of Antitumor Prodrugs - Substrates For Antibody-Targeted EnzymesW
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  215819. GABRIEL WEATHERHEAD
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  215822. Angew. Chem., Int. Ed. Engl.M
  215823. 17279N
  215824. 2/28/96V!Proteins from the D-chiral world.W
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  215827. GABRIEL WEATHERHEAD
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  215832. 2/28/96V:Multiple peptide synthesis methods and their applications.W
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  215839. 17281N
  215840. 2/28/96VHSubstituent and Solvent Effects in Intramolecular Diels-Alder Reactions.W
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  215842. GABRIEL WEATHERHEAD
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  215845. TetrahedronC.C-C BOND FORMATION /ANNULATIONS /MISCELL NEOUSM
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  215847. 2/28/96V
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  215855. 2/28/96V)Recent Advances in Double Bond Formation.W
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  215860. Aldrichimica ActaM
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  215862. 2/28/96V,Enantioselective synthesis of 
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  215871. 2/28/96V&Recent studies on the anomeric effect.W
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  215879. 2/28/96V@Second-row anomeric interactions: the involv ment of phosphorus.W
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  215881. GABRIEL WEATHERHEAD
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  215886. 2/28/96VFSome Routes to Chi al Sulfoxides with Very High Enantiomeric Excesses.W
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  215893. 2/28/96V@Divalent samarium compounds: perspectives for organic chemistry.W
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  215908. 2/28/96V#Organic Chemistry with Lanthanides.W
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  215916. 2/28/96VGAsymmetric catalysis in organic synthesis with industrial perspectives.W
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  215921. TetrahedronC ORGANOMETALLICS /LANTHANIDES /LaM
  215922. 17292N
  215923. 2/28/96V!Lanthanides in Organic Synthesis.W
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  215931. 2/28/96V
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  215954. 2/28/96VcRecommended methods for the purification of solvents and tests for impurities. Benzene and toluene.W
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  215968. 2/28/96VpRole of Protic and Dipolar Aprotic Solvents in Heterocyclic Synthesis via 1,3-Dipolar  Cycloadditions Reactions.W
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  215974. 2/28/96V%Trichloroethane in Organic Synthesis.W
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  215981. 2/28/96VIThe synthesis of radiolabeled compounds via organometallic intermediates.W
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  215989. 2/28/96VeThe Hypoiodite Reaction. (Introduction to the Intramolecular Substitution at an Unactivated  C-Atom).W
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  215995. 2/28/96VROrganoelement Derivatives of 2-Pyrone and their Applications in Organic Synthesis.W
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  215997. GABRIEL WEATHERHEAD
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  216000. Pd /NiM
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  216002. 2/28/96V\Carbon-carbon bond formation in heterocycles using nickel and palladium catalyzed reactions.W
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  216016. 2/28/96V&Fast Isomerisation About Double Bonds.W
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  216037. 2/28/96V@Peptide and protein synthesis by segment synthesi -condensation.W
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  216045. 2/28/96VTSynthetic approaches to biologically active peptides and proteins including enzymes.W
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  216050. 17310N
  216051. 2/28/96VYDi- and Polyalkali Metal Derivativ s of Heterofunctionally Substituted Organic Molecules.W
  216052. 1977X
  216053. GABRIEL WEATHERHEAD
  216054. 16302
  216055. Kaiser, E. E.B    SynthesisCaFUNCTIONAL GROUPS /DISSOLVING METAL /ARENES /Li /NH3 /LITHIUM /REDUCTION /BIRCH  /C=C-C=C /DIENESM
  216056. 17311N
  216057. 2/28/96VIA Comparison of Methods Using Lithium /Amine and Birch Reduction Systems.W
  216058. 1972X
  216059. GABRIEL WEATHERHEAD
  216060. 16303
  216061. Kaim, W.B
  216062. Top. Curr. Chem.M
  216063. 17312N
  216064. 2/28/96VhThermal and light induced electron transfer reactions of main group metal hydrides and  organometallics.W
  216065. 19 4X
  216066. GABRIEL WEATHERHEAD
  216067. 16304
  216068. Kahn, M.B
  216069. SynlettM
  216070. 17313N
  216071. 2/28/96
  216072. %VLPeptide secondary structure mimetics: recent advances and future challenges.W
  216073. 1993X
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  216075. GABRIEL WEATHERHEAD
  216076. 16305
  216077. Kagan, H. B.//Riant, O.B
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  216079. 17314N
  216080. 2/28/96V+Catalytic asymmetric Diels-Alder reactions.W
  216081. 1992X
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  216083. GABRIEL WEATHERHEAD
  216084. 16306
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  216086. 17315N
  216087. 2/28/96V*Naturally occurring di- and trithiophenes.W
  216088. 1991X
  216089. GABRIEL WEATHERHEAD
  216090. 16307
  216091. Kanner, B.B
  216092. HeterocyclesC
  216093. REAGENTSM
  216094. 17316N
  216095. 2/28/96V(2,6-Di-t-Butylpyridine. An Unusual Base.W
  216096. 1982X
  216097. GABRIEL WEATHERHEAD
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  216100. 17317N
  216101. 2/28/96V'Catalytic antibodies--designer enzymes.W
  216102. 1990X
  216103. GABRIEL WEATHERHEAD
  216104. 16309
  216105. Kanemasa, S.//Tsuge, O.B
  216106. HeterocyclesC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[3+2]M
  216107. 17318N
  216108. 2/28/96
  216109. *VURecent advances in synthetic applications of nitrile oxide cycloaddition (1981-1989).W
  216110. 1990X
  216111. GABRIEL WEATHERHEAD
  216112. 16310
  216113. +A,Kane, V. V.//De Wolf, W. H.//Bickelhaupt, F.B
  216114. TetrahedronM
  216115. 17319N
  216116. 2/28/96V
  216117. Synthesis of small cyclophanes.W
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  216119. 45 5-622Y
  216120. GABRIEL WEATHERHEAD
  216121. 16311
  216122. ,A0Kane, V. V.//Singh, V.//Martin, A.//Doyle, D. L.B
  216123. TetrahedronCVFUNCTIONAL GROUPS /PREPARATIONS /ALDEHYDES /O=C-R /KETONES /TRANSPOSITION /1,2  /O=C-RM
  216124. 17320N
  216125. 2/28/96V,The Chemistry of 1,2-Carbonyl Transposition.W
  216126. 1983X
  216127. GABRIEL WEATHERHEAD
  216128. 16312
  216129. Kamlet, M. J.B
  216130. Prog. Phys. Org. Chem.M
  216131. 17321N
  216132. 2/28/96V
  216133. Linear solvation energy relationships: An improved equation for correlation and prediction of  aqueous solubilities of aromatic solu es including polycyclic aromatic hydrocarbons and polychlorinated biphenyls.W
  216134. 1993X
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  216137. Kametani, T.//Hibino, S.B
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  216139. 17322N
  216140. 2/28/96
  216141. .V]The Synthesis of Natural Heterocyclic Products by Hetero Diels-Alder Cycloaddition Reactions.W
  216142. 1987X}246  C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /N=C-C=C /O=C-C=C  /C=N /C=O /N=S /N=O /DA /HETEROCYCLESY
  216143. GABRIEL WEATHERHEAD
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  216145. Kametani, T.//Honda, T.B
  216146. Adv. Heterocycl. Chem.CHC-C BOND FORMATION /HETEROANNULATIONS /3-RING /HETRING /3(N) /AZIRIDINESM
  216147. 17323N
  216148. 2/28/96V@Applications of Aziridines to the Synthesis of Natural Products.W
  216149. 1986X
  216150. GABRIEL WEATHERHEAD
  216151. 16315
  216152. Kametani, T.//Nemoto, H.B
  216153. TetrahedronC'C-C BOND FORMATION /ANNULATIONS /6-RINGM
  216154. 17324N
  216155. 2/28/96V^Recent Advances in the Total Synthesis of Steroids via Intramolecular Cycloaddition Reacti ns.W
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  216157. GABRIEL WEATHERHEAD
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  216159. Kametani, T.//Fukumoto, K.B    SynthesisCCFUNCTIONAL GROUPS /MISCELLANEOUS /OXIDATION /ISOQUINOLINE ALKALOIDSM
  216160. 17325N
  216161. 2/28/96
  216162. Application of Phenolic Oxidation to the Total Synthesis of the Isoquinoline and Related Alkaloids.  Biogenetic Type Synthesis.W
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  216164. GABRIEL WEATHERHEAD
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  216167. HeterocyclesM
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  216169. 2/28/96VCRecent advances in the sy thetic uses of chlorocarbonyl isocyanate.W
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  216172. GABRIEL WEATHERHEAD
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  216174. Kamal, A.//Sattur, P. B.B
  216175. HeterocyclesCLREAGENTS /CHLOROSULFONYL ISOCYANATE /O=C=N-SO2Cl /HETEROCYCLES /
  216176. -LACTAMS /SM
  216177. 17327N
  216178. 2/28/96VNChlorosulfonyl Isocyanate : A Novel Reagent for the Synthesis of Heterocycles.W
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  216181. GABRIEL WEATHERHEAD
  216182. 16319
  216183. Kalyanaraman, V.//George, M. V.B
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  216186. 17328N
  216187. 2/28/96V-Alkali Metal Addition to Unsaturated Systems.W
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  216189. GABRIEL WEATHERHEAD
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  216192. TetrahedronC=FUNCTIONAL GROUPS /TRANSFORMATIONS /C-X TO C-Y /C-NH2 /AMINESM
  216193. 17329N
  216194. 2/28/96
  216195. 5VXConversions of Primary Amino Groups into Other Functionality Mediated by Pyrylium Salts.W
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  216197. GABRIEL WEATHERHEAD
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  216200. HeterocyclesCgC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETER CYCLES /PYRIMIDINONES /PYRIMIDINETHIONESM
  216201. 17330N
  216202. 2/28/96VSSynthesis and Reactions of N-Substituted 2(1H)-Pyrimidinones and Pyrimidinethiones.W
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  216205. GABRIEL WEATHERHEAD
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  216208. Sulfur ReportsC;FUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /SM
  216209. 17331N
  216210. 2/28/96V=Acyclic dithiocarboxylic acid esters-reactions and syntheses.W
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  216216. 2/28/96V:Organic derivatives of manganese(II) in organic synthesis.W
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  216218. GABRIEL WEATHERHEAD
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  216229. 17334N
  216230. 2/28/96V9Reactions of cyclopropene derivatives with electrophiles.W
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  216235. 17335N
  216236. 2/28/96V1Phosphite synthesis of oligodeoxyribonucleotides.W
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  216241. 17336N
  216242. 2/28/96VPThe synthesis and properties of unsaturated nitro compounds of the furan series.W
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  216244. GABRIEL WEATHERHEAD
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  216249. 2/28/96V5100 Years of the Biginelli dihydropyridine synthesis.W
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  216258. 2/28/96V1Carbon Suboxide in Preparative Organic Chemistry.W
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  216265. 2/28/96VPThe Preparative Chemistry of O- and N-Functional Orthocarbonic Acid Derivatives.W
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  216270. 17340N
  216271. 2/28/96VoBenzotriazole as a synthetic auxiliary: benzotriazolylalkylations and benzotriazole-mediated  heteroalkylation.W
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  216279. 2/28/96V>Benzotriazole-Mediated Arylalkylation And HeteroarylalkylationW
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  216295. 17343N
  216296. 2/28/96V#Heterocyclic N-oxides and N-imides.W
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  216305. GABRIEL WEATHERHEAD
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  216309. 17345N
  216310. 2/28/96V+Benzotriazole: a novel synthetic auxiliary.W
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  216336. Nucleophilic substitution at saturated carbon atoms. Mechanisms and mechanistic borderlines:  evidence from studies with neutral leaving groups.W
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  216353. 2/28/96V$Heterocyclic Dithiocarboxylic Acids.W
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  216368. 2/28/96V#Synthesis of quassinoids. A review.W
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  216375. 2/28/96VAResolution of racemates by distillation with inclusion compounds.W
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  216383. 2/28/96V@Absolute asymmetric synthesis by irradiation of chiral crystals.W
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  216390. 2/28/96Vh[4+4]-Cycloaddition reaction in the total synthesis of eight membered ring containing natural  products.W
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  216404. 17357N
  216405. 2/28/96V[Photochemical Rearrangements and Fragmentation of Benzene Derivatives and Annelated Arenes.W
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  216410. Pure Appl. Chem.C
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  216413. Benzannelated cycloboranes.W
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  216418. Angew. Chem., Int. Ed. Engl.C
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  216421. 2/28/96VRNew Possible Applications of Heavy Metal Main-Group Elements in Organic Synthesis.W
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  216426. Angew. Chem., Int. Ed. Engl.COC-C BOND FORMATION /APPENDAGES /ORGANOMETALLICS /COPPER /OXIDATIVE COUPLING /CuM
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  216428. 2/28/96V-Oxidative Coupling via Organocopper Reagents.W
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  216433. Angew. Chem., Int. Ed. Engl.CHC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[3+2] /C-M /LiM
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  216450. 2/28/96VMMechanisms and rates of electrophilic substitution reactions of heterocycles.W
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  216458. 2/28/96V=Cycloaddition Reactions of Heteroaromatic Six-Membered Rings.W
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  216540. 2/28/96VKSynthesis of 6- and 7-membered phosphorus heterocycles by ring enlargement.W
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  216908. Angew. Chem., Int. Ed. Engl.CCORGANOMETALLICS /LITHIUM /MECHANISM /C-M(X) /Li(Cl) /CARBENOIDS /LiM
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  216910. 2/28/96
  216911. VdChemistry of Stable alpha-Halogeno-organolithium Compounds and the Mechanism of Carbenoid  Reaction.W
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  216913. GABRIEL WEATHERHEAD
  216914. 16418
  216915. A    Kober, F.B    SynthesisC
  216916. ORGANOMETALLICS /ARSENIC /AsM
  216917. 17427N
  216918. 2/28/96V%Aminoarsanes as  reparative Reagents.W
  216919. 1982X
  216920. GABRIEL WEATHERHEAD
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  216923. SynlettM
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  216925. 2/28/96VjRare-Earth-Metal Trifluoromethanesulfonates As Water-Tolerant  Lewis-Acid Catalysts In  Organic-Synthesis.W
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  216928. GABRIEL WEATHERHEAD
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  216931. Pure Appl  Chem.M
  216932. 17429N
  216933. 2/28/96VwSynthetic study on an antitumor antibiotic rhizoxin by using an enzymic process on prochiral  
  216934. -substituted glutarates.W
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  216937. GABRIEL WEATHERHEAD
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  216941. 17430N
  216942. 2/28/96VCMechanistic ingenuity in enzyme catalysis: dehydroquinate synthase.W
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  216944. GABRIEL WEATHERHEAD
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  216949. 17431N
  216950. 2/28/96V
  216951. Asymmetric Hydrogenation.W
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  216953. GABRIEL WEATHERHEAD
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  216956. 17432N
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  216964. 2/28/96V\Iron-mediated synthesis of heterocyclic ring systems and applications in alkaloid chemistry.W
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  216966. GABRIEL WEATHERHEAD
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  216971. 2/28/96VUPreparation and reactions of polyfunctional organozinc reagents in organic synthesis.W
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  216979. 17435N
  216980. 2/28/96V?The chemistry of polyfunctional organozinc and copper reagents.W
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  216985. 17436N
  216986. 2/28/96V'P-halogen-substituted phosphorus ylids.W
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  216995. GABRIEL WEATHERHEAD
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  216998. 17438N
  216999. 2/28/96V?Ketene Dithioacetals in Organic Synthesis: Recent Developments.W
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  217001. GABRIEL WEATHERHEAD
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  217006. 2/28/96V&Oxoniobates containing metal clusters.W
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  217009. GABRIEL WEATHERHEAD
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  217012. Pure Appl. Chem.C
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  217014. 2/28/96V?An outline of the chemistry of bis(9-borabicyclo[3.3.1]nonane).W
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  217020. 17441N
  217021. 2/28/96V
  217022. Electron transfer in the thermal and photochemical activation of electron donor-acceptor  complexes in organic and organometallic reactions.W
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  217027. Acc. Chem. Res.M
  217028. 17442N
  217029. 2/28/96VdInner-sphere electron transfer in organic chemistry. Relevance to electrophilic aromatic  nitration.W
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  217031. GABRIEL WEATHERHEAD
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  217036. 2/28/96V"Organometallic ions and ion pairs.W
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  217041. Acc. Chem. Res.CIPHYSICAL ORGANIC /MECHANISMS /ORGANOMETALLICS /C-M /ELECTRON TRANSFER /ETM
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  217043. 2/28/96
  217044. VUElectron-Transfer Mechanisms for Organometallic Intermediates in Catalytic Reactions.W
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  217046. GABRIEL WEATHERHEAD
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  217051. 2/28/96V>Opportunities in asymmetric synthesis: an industrial prospect.W
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  217059. 2/28/96VHThe Histrionicotoxins:  ynthesis of 1-Azaspiro[5.5]undecane Ring System.W
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  217061. GABRIEL WEATHERHEAD
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  217065. 17447N
  217066. 2/28/96V+o-Hydroxyaryl ketones in organic synthesis.W
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  217075. The chemistry of 1,3-dioximes.W
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  217080. Heterocycles
  217081. 17449N
  217082. 2/28/96V0Pyrazole 1-oxides, 1,2-dioxides and derivatives.W
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  217085. GABRIEL WEATHERHEAD
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  217089. 17450N
  217090. 2/28/96V.Gem-di-halocyclopropanes in organic synthesis.W
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  217095. 17451N
  217096. 2/28/96V
  217097. Halogen-containing carbenes.W
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  217102. TetrahedronCFC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETRING /6(N)M
  217103. 17452N
  217104. 2/28/96V*Pyridine Ring Nucleophilic Recyclisations.W
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  217112. 2/28/96V1The Synthesis of Phosphonic and Phosphinic Acids.W
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  217119. 2/28/96
  217120. V3Asymmetric synthesis of chiral macrocyclic ligands.W
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  217128. 2/28/96V1Synthetic aspects of electron-transfer chemistry.W
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  217133. Angew. Chem., Int. Ed. Engl.C8PHYSICAL ORGANIC /MECHANISMS /RADICAL ANION /SUBSITUTIONM
  217134. 17456N
  217135. 2/28/96VESubstitution Reactions Which Proc ed via Radical Anion Intermediates.W
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  217142. 2/28/96V9The Synthesis of Aliphatic and Alicyclic Nitro Compounds.W
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  217149. 2/28/96V<Replacement of the Aromatic Primary Amino Group by Hydrogen.W
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  217163. 17460N
  217164. 2/28/96VCSynthesis and biological properties of selected nucleoside analogs.W
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  217173. 2/28/96V1The Isoxazoline Route to the Molecules of Nature.W
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  217179. 17462N
  217180. 2/28/96V'Transition Metals in Organic Synthesis.W
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  217221. 2/28/96V>Advances in the chemistry of sulfimides and related compounds.W
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  217235. 2/28/96V=Progress in the chemistry of perhalomethanesulphenyl halides.W
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  217241. 2/28/96V2Advances in the chemistry of sulphenic acid amidesW
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  217247. 2/28/96V*Progress in the chemistry of sulfilimines.W
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  217254. 2/28/96V/Methods for the synthesis of alpha-keto esters.W
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  217262. 2/28/96VlBicyclic ketals: versatile intermediates for the stereocontrolled construction of cyclic ether  derivatives.W
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  217278. 2/28/96VFOrganic Synthesis Using Bridgehead Carbocations and Bridgehead Enones.W
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  217293. 2/28/96VBSynthesis of Carbocyclic Spiro Compounds via Rearrangement Routes.W
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  217300. 2/28/96VJImproved methods fo  the synthesis of aza-crown macrocycles and cryptands.W
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  217330. HeterocyclesC~C-C BOND FORMATION /HETEROANNULATIONS /3-RING /SELENIUM /C-M(X) /Li(Se) /X-C-C-Y  /O,Se /HETRING /3(O) /EPOXIDES /OXIRANES /SeM
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  217332. 2/28/96VFOriginal Syntheses of Epoxides Involving Org noselenium Intermediates.W
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  217335. GABRIEL WEATHERHEAD
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  217338. Top. Curr. Chem.M
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  217340. 2/28/96V
  217341. Synthesis and Synthetic Applications of 1-Metallo-1-seleno-cyclopropanes and -cyclobutanes and  Related 1-Metallo-1-silyl-cyclopropanes.W
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  217343. 1-75Y
  217344. GABRIEL WEATHERHEAD
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  217346. A    Krief, A.B
  217347. TetrahedronC"ORGANOMETALLICS /SYNTHESIS /C-M(X)M
  217348. 17485N
  217349. 2/28/96V@Synthetic Methods Using alpha-Heterosubstituted Organometallics.W
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  217351. 2531Y
  217352. GABRIEL WEATHERHEAD
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  217354. Kricka, L. J.//Ledwith, A.B    SynthesisC'C-C BOND FORMATION /ANNULATIONS /4-RINGM
  217355. 17486N
  217356. 2/28/96VkCyclobutanes from Photochemical, Metal-Catalysed, and Cation-Radical Induced Dimerisation of  Mono-Olefins.W
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  217358. GABRIEL WEATHERHEAD
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  217360. Kresge, A. J.B
  217361. Acc. Chem. Res.M
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  217363. 2/28/96VOFlash photolytic generation and study of reactive species: from enols to ynols.W
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  217365. GABRIEL WEATHERHEAD
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  217367. Krechl, J.//Castulik, P.B
  217368. Chem. Scr.M
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  217370. 2/28/96V$Enzyme models based on cyclodextrin.W
  217371. GABRIEL WEATHERHEAD
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  217375. 2/28/96V]Neutral acyclic analogues of crown-ethers and cryptands and their complex-forming properties.W
  217376. 1990X
  217377. GABRIEL WEATHERHEAD
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  217379. Krohnke, F.B    SynthesisCFC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETRING /6(N)M
  217380. 17490N
  217381. 2/28/96V7The  pecific Synthesis of Pyridines and Oligopyridines.W
  217382. 1976X
  217383. GABRIEL WEATHERHEAD
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  217385. A    Krohn, K.B
  217386. TetrahedronC]C-C BOND FORMATION /AROMATICS /RING FORMATION /CARBOHYDRATES /O=C(R)-C-X /(O)OH  /LACTIC ACIDM
  217387. 17491N
  217388. 2/28/96V[Synthesis of Anthracyclinones by Electrophilic and Nucleophilic Addition to Anthraquinones.W
  217389. 1990X
  217390. GABRIEL WEATHERHEAD
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  217392. A    Krohn, K.B5Progress in the Chemistry  f Organic Natural ProductsM
  217393. 17492N
  217394. 2/28/96V<Building blocks for the total synthesis of anthracyclinones.W
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  217396. GABRIEL WEATHERHEAD
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  217398. Krogh, E.//Wan, P.B
  217399. Top. Curr. Chem.M
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  217401. 2/28/96V>Photoinduced electron transfer of carbanions and carbocations.W
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  217403. GABRIEL WEATHERHEAD
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  217405. Krimen, L. I.//Cota, D. J.B
  217406. Org. React. (N.Y.)C
  217407. NAME REACTIONS /RITTER REACTIONM
  217408. 17494N
  217409. 2/28/96V
  217410. The Ritter Reaction.W
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  217412. GABRIEL WEATHERHEAD
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  217414. Krylov, . V.B Russ. Chem. Rev. (Engl. Transl.)M
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  217416. 2/28/96V]Methods for increasing the efficiency of catalysis for the oxidative condensation of methane.W
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  217418. GABRIEL WEATHERHEAD
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  217421. 17496N
  217422. 2/28/96VOThe partial catalytic oxidation of methane to give oxygen-containing compounds.W
  217423. 1992X
  217424. 1118Y
  217425. GABRIEL WEATHERHEAD
  217426. 16488
  217427. Krow, G. R.B
  217428. Org. React. (N.Y.)M
  217429. 17497N
  217430. 2/28/96V7The Baeyer-Villiger Oxidation of Ketones and Aldehydes.W
  217431. 1993X
  217432. 251-798Y
  217433. GABRIEL WEATHERHEAD
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  217435. Krow, G. R.B
  217436. Tetrahedron
  217437. C/C-C BOND FORMATION /ANNULATIONS /RING EXPANS ONM
  217438. 17498N
  217439. 2/28/96V7One Carbon Ring Expansions of Bridged Bicyclic Ketones.W
  217440. 1987X
  217441. GABRIEL WEATHERHEAD
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  217443. Krow, G. R.B
  217444. TetrahedronC
  217445. C-C BOND FORMATION /ANNULATIONS /RING EXPANSION /PHYSICAL ORGANIC /REARRANGEMENTS  /KETONES /BAEYER-VILLIGER REACTION /LACTONESM
  217446. 17499N
  217447. 2/28/96V7Oxygen Insertion Reactions of Bridged Bicyclic Ketones.W
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  217449. 2697Y
  217450. GABRIEL WEATHERHEAD
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  217452. Krow, G. R.B
  217453. TetrahedronC
  217454. C-C BOND FORMATION /ANNULATIONS /RING EXPANSION /PHYSICAL ORGANIC /REARRANGEME TS /KETONES /RING EXPANXION BECKMANN REACTION SCHMIDT REACTION /LACTAMSM
  217455. 17500N
  217456. 2/28/96VZNitrogen Insertion Reactions of Bridged Bicyclic Ketones, Regioselective Lactam Formation.W
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  217459. GABRIEL WEATHERHEAD
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  217461. Krow, G. R.B
  217462. Angew. Chem., Int. Ed. Engl.CyFUNCTIONAL GROUPS /PREPARATIONS /HETEROCUMULENES /C=C=N-R /X=Y=Z /C,C,N  /KETENIMINES /C=C=N-R /X=Y=Z /C,C,N /KETENIMINESM
  217463. 17501N
  217464. 2/28/96
  217465. V'Synthesis and Reactions of Ketenimines.W
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  217467. GABRIEL WEATHERHEAD
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  217470. Angew. Chem., Int. Ed. Engl.M
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  217472. 2/28/96VCC60: Buckminsterfullerene, the celestial sphere that fell to earth.W
  217473. 1992X
  217474. GABRIEL WEATHERHEAD
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  217479. 2/28/96V
  217480. C60: Buckminsterfullerene.W
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  217487. 2/28/96VZCarbene methods for the introduction of acyl and acylmethyl groups into organic molecules.W
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  217493. 2/28/96V1Deoxygenation of coordinated and free sulfoxides.W
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  217499. 2/28/96
  217500. V>The synthesis of insect juvenile hormones and their analogues.W
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  217502. GABRIEL WEATHERHEAD
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  217506. 2/28/96V*Aliphatic fluorine-containing amino acids.W
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  217512. 2/28/96V 
  217513. -Fluoro-substituted aminoacids.W
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  217519. 2/28/96V)Fluorine-containing aromatic amino acids.W
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  217525. F /PM
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  217527. 2/28/96VTAsymmetric synthesis of fluorine- and phosphorus-containing analogues of aminoacids.W
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  217529. GABRIEL WEATHERHEAD
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  217531. Kuivila, H. G.B    SynthesisCOFUNCTIONAL GROUPS /METAL HYDRIDE /C-X /Br,I /R3SnH /HALIDES /REDUCTION /C-H /SnM
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  217533. 2/28/96V5Reduction of Organic Compounds by Organotin Hydrides.W
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  217535. GABRIEL WEATHERHEAD
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  217537. A    Kuhle, E.B    SynthesisC
  217538. FUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C-C BOND FORMATION  /HETEROANNULATIONS /5-RING /C-X /SCl /C-X /SBr /SULFENYL HALIDES /SUBSTITUTION  /CYCLISATION /HETRING 5(S) /TETRAHYDROTHIOP ENES /SM
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  217540. 2/28/96VoOne Hundred Years of Sulfenic Acid Chemistry: IIb. Substitution and Cyclisation Reactions of  Sulfenyl Halides.W
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  217544. A    Kuhle, E.B    Synthes sCpFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C-X /SCl /C-X /SBr  /OXIDATION /REDUCTION /ADDITION /SM
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  217546. 2/28/96VuOne Hundred Years of Sulfenic Acid Chemistry: IIa. Oxidation, Reduction, and Addition Reactions of  Sulfenyl Halides.W
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  217551. Tetrahedron Symposium-in-PrintC1TARGET SYNTHESIS /MISCELLANEOUS /INDOLE ALKALOIDSM
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  217553. 2/28/96V%New Developments in Indole Alkaloids.W
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  217561. 2/28/96V5The structure and mechanism of formation of ozonides.W
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  217568. 2/28/96V$Formation and Structure of Ozonides.W
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  217574. P /SM
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  217576. 2/28/96VQThe reactivity of phosphorus-containing sulfenyl chlorides in addition reactions.W
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  217578. GABRIEL WEATHERHEAD
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  217580. Kutyrev, A. A.B
  217581. TetrahedronM
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  217583. 2/28/96V#Nucleophilic reactions of quinones.W
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  217588. Kuthan, J.//Sebek, P.//Bohm, S.B
  217589. Adv. Heterocycl. Chem.C    S /Se /TeM
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  217591. 2/28/96VLDevelopments in the chemistry of thiopyrans, selenopyrans, and teluropyrans.W
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  217595. A.Kutateladze, A. G.//Zefirov, N. S.//Zyk, N. V.B
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  217598. 2/28/96VyReactions of sulfenic and sulfosylic acid derivatives with olefins in the presence of sulfur trioxide  and its complexes.W
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  217602. A+Kursanov, D. N.//Parnes, Z. N.//Loim, N. M.B    SynthesisCDFUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDE /HYDRIDES /LiAlH4 /NaBH4M
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  217604. 2/28/96V9Applications of Ionic Hydrogenation to Organic Synthesis.W
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  217610. 2/28/96V<Synthesis of spirone-[piperidine-4,C'n-hetero(carbo)cycles].W
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  217619. 2/28/96VsMolecular basis of catalytic reactions involving trihapto-allyl complexes of group 10 metals as  key intermediates.W
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  217626. 2/28/96VACarbohydrates as chiral auxiliaries in stereoselective synthesis.W
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  217634. 2/28/96VIRecent Advances in Arene Transformation Reactions via Chromium Complexes.W
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  217638. Kumada, M.B
  217639. Acc. Chem. Res.C[C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /ORGANOMETALLICS  /SYNTHESIS /Fe /TMM
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  217641. 2/28/96VuAsymmetric Synthesis Catalysed by Transition-Metal Complexes with Functionalised Chiral  Ferrocenylphosphine Ligands.W
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  217645. Kumada, M.B
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  217647. CY C-C BOND FORMATION /APPENDAGES /COUPLING /NICKEL /PALLADIUM /C-M /R-X /COUPLING /Ni  /PdM
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  217649. 2/28/96ViNickel and Palladium Catalysed Cross-Coupling Reactions of Organometallic Reagents with Organic  Halides.W
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  217657. Carboxyolefination.W
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  217663. 2/28/96VWActivated cyclopropanes in the synthesis of five-membered carbocycles and heterocycles.W
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  217669. 2/28/96VOReactions involving the a dition of N-halogeno amides to unsaturated compounds.W
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  217677. 2/28/96VCConocurvone - prototype of a new class of anti-HIV active compound?W
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  217684. C-C BOND FORMATION /ANNULATIONS /CYCLOADDITIONS /AROMATICS /PHOTOCHEMICAL  REACTIONS /PHOTOCHEMISTRY /Ar-C=C / RENES /ALKENES /ARYLOLEFINS /CYCLISATIONM
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  217686. 2/28/96VWPhotochemical Cyclisations and Intramolecular Cycloadditions of Conjugated Arylolefins.W
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  217693. 2/28/96V/Supramolecular assemblies based on calixarenes.W
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  217709. 2/28/96V0Some Aspects Of Biocatalysis In Organic-SolventsW
  217710. 1994X    8253-8274Y
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  217716. 2/28/96VDBenzo[c]pyrilium salt syntheses, reactions, and physical properties.W
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  217722. 2/28/96VDThe present state of the chemistry of aminonitrenes and oxynitrenes.W
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  217728. 2/28/96V?Azaadamantanes with n trogen atoms in the bridgehead positions.W
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  217735. 2/28/96V The photochemistry of coumarins.W
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  217737. GABRIEL WEATHERHEAD
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  217745. GABRIEL WEATHERHEAD
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  217748. Top. Curr. Chem.CFORGANOMETALLICS /TITANIUM  ZINC /CARBRING /3 /O=C(R)-C-C-X /Ti /Zn /SiM
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  217750. 2/28/96V,Metal homoenolates from siloxycyclopropanes.W
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  217752. GABRIEL WEATHERHEAD
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  217755. Pure Appl. Chem.C
  217756. HOMOENOLATESM
  217757. 17542N
  217758. 2/28/96VE1-Alkoxy-1-siloxycyclopropanes as homoenolate nucleophiles of esters.W
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  217760. GABRIEL WEATHERHEAD
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  217762. Kuwajima, I.//N kamura, E.B
  217763. Acc. Chem. Res.CIC-C BOND FORMATION /APPENDAGES /ENOLATES /C=C-X /OSi /ENOLATES /C=C-X /LiM
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  217765. 2/28/96V)Reactive Enolates from Enol Silyl Ethers.W
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  217767. GABRIEL WEATHERHEAD
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  217769. Lane, C. F.//Kabalka, G. W.B
  217770. TetrahedronC-REAGENTS /CATECHOLBORANE /HYDROMETALLATION /BM
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  217772. 2/28/96V,Catecholborane. A New Hydroboration Reagent.W
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  217774. GABRIEL WEATHERHEAD
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  217776. Lane, C. F.B
  217777. Chem. Rev.C=FUNCTIONAL GROUPS /METAL HYDRIDE /DIBORANE /BH3 /REDUCTION /BM
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  217780. V-Reduction of Organic Comp unds with Diborane.W
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  217782. GABRIEL WEATHERHEAD
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  217784. Lane, C. F.B    SynthesisC5REAGENTS /REDUCTION /SODIUM CYANOBOROHYDRIDE /NaBH3CNM
  217785. 17546N
  217786. 2/28/96V]Sodium Cyanoborohydride - A Highly Effective Reducing Agent for Organic Functional Compounds.W
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  217788. GABRIEL WEATHERHEAD
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  217793. 2/28/96V?Organic dications: Gas-phase experiments and theory in concert.W
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  217795. GABRIEL WEATHERHEAD
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  217800. 2/28/96VyAre Polar Organometallic Compounds Carbanions - The Gegenion Effect On  Structure And Energies  Of Alkali-Metal CompoundsW
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  217802. GABRIEL WEATHERHEAD
  217803. 16540
  217804. Lambert, J. B.B
  217805. TetrahedronC@PHYSICAL ORGANIC /STEREOELECTRONICS /CARBONIUM IONS /SILICON /SiM
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  217807. 2/28/96
  217808. V:The Interaction of Silicon with Positively Charged Carbon.W
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  217811. GABRIEL WEATHERHEAD
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  217813. A:Lambert, J. B.//Mark, H. W.//Holcomb, A. G.//Magyar, E. S.B
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  217817. 2/28/96V9Inductive Enhancement of Neighboring Group Participation.W
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  217819. GABRIEL WEATHERHEAD
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  217823. 2/28/96VHUse of Organosilicon Reagents as Protective Groups in Organic Synthesis.W
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  217825. GABRIEL WEATHERHEAD
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  217827. A-Lalancette, J. M.//Freche, A.//Brindle, J. R.B    SynthesisC`FUNCTIONAL GROUPS / EDUCTION /METAL HYDRIDE /NaBH4 /BOROHYDRIDE /O=C /KETONES /C-X /OH /ALCOHOLSM
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  217829. 2/28/96V_Reductions of Functional Groups with Sulfurated Borohydrides. Application to Steroidal Ketones.W
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  217831. GABRIEL WEATHERHEAD
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  217834. Nat. Prod. Rep.
  217835. C>TARGET SYNTHESIS /PROSTAGLANDINS /LEUKOTRIENES /PROSTAGLANDINSM
  217836. 17553N
  217837. 2/28/96VUProstaglandins, Thromboxanes, Leukotrienes, and Related Arachidonic Acid Metabolites.W
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  217839. GABRIEL WEATHERHEAD
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  217841. Lai, Y. H.B    SynthesisC
  217842. ORGANOMETALLICS /MAGNESIUM /MgM
  217843. 17554N
  217844. 2/28/96V6Grignard Reagents from Chemically Activated Magnesium.W
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  217849. Chem. Rev.C
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  217852. 2/28/96V?Stereochemistry of Organometallic Compound Addition to Ketones.W
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  217854. GABRIEL WEATHERHEAD
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  217857. Pure Appl. Chem.C
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  217859. 2/28/96VCNew applications of organopalladium compounds in organic synthesis.W
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  217861. GABRIEL WEATHERHEAD
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  217863. Larock, R. C.B
  217864. TetrahedronC!ORGANOMETALLICS /MERCURY /C-X /HgM
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  217867. V&Organomercurials in Organic Synthesis.W
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  217870. GABRIEL WEATHERHEAD
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  217873. J. Organomet. Chem.C ORGAN METALLICS /LANTHANIDES /LaM
  217874. 17558N
  217875. 2/28/96V1Bis(h-cyclopentadienyl)lanthanoid(III) Chlorides.W
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  217881. 2/28/96VdCatalytic synthesis of organic compounds by carbonylation of unsaturated hydrocarbons and  alcohols.W
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  217883. GABRIEL WEATHERHEAD
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  217887. 2/28/96VgThe azinyl-azinylid ne tautomerism of azinylmethanes and general problems of the tautomerism of azines.W
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  217891. Lansbury, P. T.B
  217892. Acc. Chem. Res.C2C-C BOND FORMATION /ANNULATIONS /6-RING /C=C-X /ClM
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  217902. 2/28/96V-Novel carbon compounds with 'naked' Cn units.W
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  217908. Quarterly ReviewsC
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  217911. 2/28/96V
  217912. Organothallium Chemistry.X
  217913. GABRIEL WEATHERHEAD
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  217915.  A)LeBozec, H.//Touchard, D.//Dixneuf, P. H.B
  217916. Adv. Organomet. ChemM
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  217918. 2/28/96VAOrganometallic chemistry of arene ruthenium and osmium complexes.W
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  217922. Le Noble, W. J.B    SynthesisC4C-C BOND FORMATION /APPENDAGES /ENOLATES /ALKYLATIONM
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  217924. 2/28/96V1Conditions for the Alkylation of Ambident Anions.W
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  217926. GABRIEL WEATHERHEAD
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  217929. Sulfur ReportsC
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  217931. 2/28/96V
  217932. Electrochemical activation of sulfur in organic solvents - new syntheses o  thioorganic compounds with a sacrificial carbon - sulfur electrode.W
  217933. 1992X
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  217938. SynlettM
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  217940. 2/28/96VwRing opening reactions o  oxabicyclic compounds as a route to cyclic and acyclic compounds with multiple stereocenters.W
  217941. 1993X
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  217946. Pure Appl. Chem.M
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  217948. 2/28/96V6New methods for the control of multiple stereocenters.W
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  217954. Pure Appl. Chem.M
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  217956. 2/28/96V3Cata ysis of organic reactions by inorganic solids.W
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  217959. GABRIEL WEATHERHEAD
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  217962. Acc. Chem. Res.C%ODDS AND ENDS /TECHNIQUES AND METHODSM
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  217964. 2/28/96V3Catalysis of Organic Reactions by Inorganic Solids.W
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  217968. Lasne, M.-C.//Ripoll, J.-L.B    SynthesisCOC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /CYCLOREVERSIONM
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  217970. 2/28/96V9New Synthetic Developments of the [4 +2 ] Cycloreversion.W
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  217972. GABRIEL WEATHERHEAD
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  217975. Pure Appl. Chem.M
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  217977. 2/28/96VKSpecific reactions of organylmetal complexes with unsaturated hydrocarbons.W
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  217979. GABRIEL WEATHERHEAD
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  217981. Lehmkuhl, H.B
  217982. Bull. Soc. Chim. Fr.C[ORGANOMETALLICS /MAGNESIUM /ZINC /C-M /C=C /CARBOMETALLATION /Mg /Zn /METAL-ENE  /INSERTIONM
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  217984. 2/28/96V1The Insertion of Olefins int  Metal-Carbon Bonds.W
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  217986. GABRIEL WEATHERHEAD
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  217992. 2/28/96VICp'M(NO)R2: 16-electron piano-stool molecules of molybdenum and tungsten.W
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  217997. Org. React. (N.Y.)M
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  217999. 2/28/96V5The Amination of Heterocyclic Bases by Alkali Amides.W
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  218001. GABRIEL WEATHERHEAD
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  218003. Lee-Ruff, E.B
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  218007. 2/28/96V$The Organic Chemistry of Superoxide.W
  218008. 1977X
  218009. GABRIEL WEATHERHEAD
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  218014. 2/28/96V\The Chemistry Of [1n] Orthocyclophanes - New Classes Of Ionophores,  Starands And Ketonands.W
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  218022. 2/28/96VaReactions of the atomic oxygen rad cal anion and the synthesis of organic reactive intermediates.W
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  218025. GABRIEL WEATHERHEAD
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  218028. Acc. Chem. Res.C
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  218030. 2/28/96V\Heterogeneous, platinum-catalyzed hydrogenations of (diolefin)dialkylplatinum(II) complexes.W
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  218032. GABRIEL WEATHERHEAD
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  218035. Chem. Ind. (London)M
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  218037. 2/28/96V4Buckminsterfullerene: the third allotrope of carbon.W
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  218039. GABRIEL WEATHERHEAD
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  218043. 17581N
  218044. 2/28/96VBStereoelectronic Origin of the Intrinsic Barrier to SN2 Reactions.W
  218045. 1990X
  218046. GABRIEL WEATHERHEAD
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  218048. Lewis, J. R.B
  218049. Nat. Prod. Rep.M
  218050. 17582N
  218051. 2/28/96VaMuscarine, oxazole, imidazole, thiazole, and peptide al aloids and other miscellaneous alkaloids.W
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  218054. GABRIEL WEATHERHEAD
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  218057. Pure Appl. Chem.M
  218058. 17583N
  218059. 2/28/96VCStyren -amine and stilbene-amine intramolecular addition reactions.W
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  218062. GABRIEL WEATHERHEAD
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  218064. Lever, O. W.B
  218065. TetrahedronC
  218066. PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBANIONS /SYNTHONS /C-M(X)(Y)  /Li(S)(S) /DITHIANES /C=C-M(X) /Li(O) /O=C-R /O=C-H /ACYLATION /1,2-ADDITIONM
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  218068. 2/28/96VHNew Horizons in Carbonyl Chemistry: Reagents for Nucleophilic Acylation.W
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  218071. GABRIEL WEATHERHEAD
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  218073. Leuenberger, H. G. W.B
  218074. Pure Appl. Chem.M
  218075. 17585N
  218076. 2/28/96VhInterrelations of chemistry and biotechnology. I. Biotransformation-a useful tool in organic  chemistry.W
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  218078. GABRIEL WEATHERHEAD
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  218081. Chemtracts: Organic ChemistryM
  218082. 17586N
  218083. 2/28/96VDObservations in the interface between immunochemistry and chemistry.W
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  218085. GABRIEL WEATHERHEAD
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  218088. Angew. Chem., Int. Ed. Engl.CJPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS /C+M
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  218091. Degenerate Carbonium Ions.W
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  218093. GABRIEL WEATHERHEAD
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  218096. Contemporary Organic SynthesisM
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  218098. 2/28/96V:Control of Asymmetry through Conjugate Addition Reactions.W
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  218101. GABRIEL WEATHERHEAD
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  218103. Lenoir, D.B    SynthesisC
  218104. ORGANOMETALLICS /TITANIUM /COUPLING /Ti /PINACOL /DEOXYGENATION /REDUCTIVE  ELIMINATION /ALKYLIDENATION /ANNULATION /12-RIN , 10-RING, 8-RING, 14-RING, 15-RING, 11-RING /DIOLS /1,2M
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  218106. 2/28/96VEThe application of low-valent titanium reagents in organic synthesis.W
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  218108. GABRIEL WEATHERHEAD
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  218110. :ABLemmen, P.//Richter, W.//Werner, B.//Karl, R.//Stumpf, R.//Ugi, I.B    SynthesisC
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  218112. 2/28/96VDFive-membered cyclic phosphorylating reagents and related compounds.W
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  218114. GABRIEL WEATHERHEAD
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  218117. Angew. Chem., Int. Ed. Engl.C
  218118. ODDS AND ENDSM
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  218120. 2/28/96V
  218121. Perspectives in supramolecular chemistry. From molecular recognition toward molecular  information processing and self-organization.W
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  218124. GABRIEL WEATHERHEAD
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  218126. Lickiss, P. D.B
  218127. Chem. Soc. Rev.C
  218128. Si /TMM
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  218130. 2/28/96VQTransition metal complexes of  ilylenes, silenes, disilenes, and related species.W
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  218132. GABRIEL WEATHERHEAD
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  218134. Lichtenthaler, F. W.B
  218135. Angew. Chem., Int. Ed. Engl.CjC-C BOND FORMATION /ANNULATIONS /5-RING /6-RING /7-RING /MeNO2 /ALDEHYDE  /NITROMETANE /H-C=O /DIALDEHYDESM
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  218137. 2/28/96V-Cyclisation of Dialdehydes with Nitromethane.W
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  218139. GABRIEL WEATHERHEAD
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  218141. Liaaen-Jensen, S.
  218142. New Journal of ChemistryM
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  218144. 2/28/96V#Marine carotenoids-selected topics.W
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  218146. GABRIEL WEATHERHEAD
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  218148. ?A    Li, C. J.B
  218149. Chem. Rev.M
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  218151. 2/28/96VROrganic reactions in aqueous media - with a focus on carbon-carbon bond formation.W
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  218154. GABRIEL WEATHERHEAD
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  218157. Recl. Trav. Chim. Pays-BasM
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  218159. 2/28/96V;Competing concepts in electronic control of face selection.W
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  218162. GABRIEL WEATHERHEAD
  218163. 16588
  218164. Li, S.//Purdy, W. C.B
  218165. Chem. Rev.M
  218166. 17597N
  218167. 2/28/96V=Cyclodextrins and their applications in analytical chemistry.W
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  218170. GABRIEL WEATHERHEAD
  218171. 16589
  218172. Leznoff, C. C.B
  218173. Acc. Chem. Res.CAODDS AND ENDS /TECHNIQUES AND METHODS /INSOLUBLE POLYM R SUPPORTSM
  218174. 17598N
  218175. 2/28/96VCThe Use of Insoluble Polymer Supports in General Organic Synthesis.W
  218176. 1978X
  218177. GABRIEL WEATHERHEAD
  218178. 16590
  218179. CA7Ley, S. V.//Norman, J.//Griffith, W. P.//Marsden, S. P.B    SynthesisC
  218180. 17599N
  218181. 2/28/96V_Tetrapropylammonium Perruthenate, Pr4N+RuO4-, TPAP : Catalytic  Oxidant For Organic  Synthesis.W
  218182. 1994X
  218183. 639-666a
  218184. GABRIEL WEATHERHEAD
  218185. 16591
  218186. DA$Ley, S. V.//Denholm, A. A.//Wood, A.B
  218187. Nat. Prod. Rep.M
  218188. 17600N
  218189. 2/28/96V
  218190. The chemistry of azadirachtin.W
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  218192. 109-57Y
  218193. GABRIEL WEATHERHEAD
  218194. 16592
  218195. Ley, S. V.//Toogood, P. L.B    Chem. Br.M
  218196. 17601N
  218197. 2/28/96V
  218198. Insect antifeedants.W
  218199. 1990X
  218200. GABRIEL WEATHERHEAD
  218201. 16593
  218202. Lewis, J. R.B
  218203. Nat. Prod. Rep.M
  218204. 17602N
  218205. 2/28/96V'Amaryllidaceae and Sceletium alkaloids.W
  218206. 1993X
  218207. 291-9Y
  218208. GABRIEL WEATHERHEAD
  218209. 16594
  218210. GA!Lipkowitz, K. B.//Peterson, M. A.B
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  218212. 17603N
  218213. 2/28/96V)Molecular mechanics in organic synthesis.W
  218214. 1993X
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  218216. GABRIEL WEATHERHEAD
  218217. 16595
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  218220. 17604N
  218221. 2/28/96V3Photochemistry of hydroxamic acids and derivatives.W
  218222. 1991X
  218223. GABRIEL WEATHERHEAD
  218224. 16596
  218225. Liotta, D., Ed.B
  218226. Tetrahedron Sy posium-in-PrintC
  218227. ORGANOMETALLICS /SELENIUM /SeM
  218228. 17605N
  218229. 2/28/96V+Recent Aspects of Organoselenium Chemistry.W
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  218232. GABRIEL WEATHERHEAD
  218233. 16597
  218234. Liotta, D.B
  218235. Acc. Chem. Res.C
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  218237. 17606N
  218238. 2/28/96V
  218239. New Organoselenium Methodology.W
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  218241. GABRIEL WEATHERHEAD
  218242. 16598
  218243. KA Linford, L.//Raubenheimer, H. G.B
  218244. Adv. Organomet. Chem.C
  218245. S /SiM
  218246. 17607N
  218247. 2/28/96VTFormation and reactions of organosulfur and organoselenium organometallic compounds.W
  218248. 1991X
  218249. GABRIEL WEATHERHEAD
  218250. 16599
  218251. Lindley, J. A.B
  218252. TetrahedronCsC-C BOND FORMATION /AROMATICS /RING F NCTIONALISATION /ORGANOMETALLICS /COPPER /Ar-X /Br /Ar-X /I /ARENES /Ar-C /CuM
  218253. 17608N
  218254. 2/28/96V:Copper Assisted Nucleophilic Substitution of Aryl Halogen.W
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  218256. 1433Y
  218257. GABRIEL WEATHERHEAD
  218258. 16600
  218259. Lin, G.B
  218260. Pure Appl. Chem.M
  218261. 17609N
  218262. 2/28/96
  218263. MVlStructural elucidation and chiral syntheses of insect pheromones and extension of the synthetic  approaches.W
  218264. 1993X
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  218266. GABRIEL WEATHERHEAD
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  218268. Lim, S. C.//Kim, K. S.B
  218269. Pure Appl. Chem.M
  218270. 17610N
  218271. 2/28/96VYActivation of superoxide: application of peroxysulfur intermediates to organic synthesis.W
  218272. 1993X
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  218274. GABRIEL WEATHERHEAD
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  218277. 17611N
  218278. 2/28/96V;Catalytic chemistry and technology of one carbon compounds.W
  218279. 1989X
  218280. GABRIEL WEATHERHEAD
  218281. 16603
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  218283. SynlettM
  218284. 17612N
  218285. 2/28/96VUOmega-Aminoalkylheterocycles - Actual Aspects Of The Chemistry Of  Histamine Analogs.W
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  218287. GABRIEL WEATHERHEAD
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  218289. QADLittle, R. D.//Masjedizadeh, M. R.//Moeller, K. D.//Dannecker, D. I.B
  218290. SynlettC'C-C BOND FORMATION /ANNULATIONS /5-RINGM
  218291. 17613N
  218292. 2/28/96
  218293. QVPFactors affecting regioselectivity in the intramolecular diyl trapping reaction.W
  218294. 1992X
  218295. GABRIEL WEATHERHEAD
  218296. 16605
  218297. Little, R. D.B
  218298. Chem. Rev.C'C-C BO D FORMATION /ANNULATIONS /5-RINGM
  218299. 17614N
  218300. 2/28/96VOThe Intramolecular Diyl Trapping Reaction. A Useful Tool for Organic Synthesis.W
  218301. 1986X
  218302. GABRIEL WEATHERHEAD
  218303. 16606
  218304. Liskamp, R. M. J.B
  218305. Recl. Trav. Chim. Pays-BasM
  218306. 17615N
  218307. 2/28/96VoConformationally restricted amino acids and dipeptides, (non)peptidomimetics and secondary  structure mimetics.W
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  218310. GABRIEL WEATHERHEAD
  218311. 16607
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  218313. Angew. Chem., Int. Ed. Engl.M
  218314. 17616N
  218315. 2/28/96VY A new application of modified peptides and peptidomimetics: potential anticancer agents.W
  218316. 1994X
  218317. 305-7Y
  218318. GABRIEL WEATHERHEAD
  218319. 16608
  218320. Lipshutz, B. H.//Sengupta, S.B
  218321. Org. React. (N.Y.)C
  218322. 17617N
  218323. 2/28/96VgOrganocopper reagents: Substitution, conjugate addition, carbo /metallocupration, and other  reactions.
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  218325. GABRIEL WEATHERHEAD
  218326. 16609
  218327. Lipshutz, B. H.B
  218328. SynlettC
  218329. ORGANOMETALLICS /COPPER /CuM
  218330. 17618N
  218331. 2/28/96V,The Evolution of Higher Order Cyanocup ates.W
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  218333. GABRIEL WEATHERHEAD
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  218335. Lipshutz, B. H., Ed.B
  218336. Tetrahedron Symposium-in-PrintC ORGANOMETALLICS /COPPER /C-M /CuM
  218337. 17619N
  218338. 2/28/96V.Recent Developments in Organocopper Chemistry.W
  218339. 1989X
  218340. GABRIEL WEATHERHEAD
  218341. 16611
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  218343. ORGANOMETALLICS /COPPER /CuM
  218344. 17620N
  218345. 2/28/96VGApplications of Higher-Order Mixed Organocuprates to Organic Synthesis.W
  218346. 1987X
  218347. GABRIEL WEATHERHEAD
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  218350. Chem. Rev.C
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  218352. 17621N
  218353. 2/28/96VIFive-Membered Heteroaromatic Rings as Intermediates in Organic Synthesis.W
  218354. 1986X
  218355. GABRIEL WEATHERHEAD
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  218357. ZA1Lipshutz, B. H.//Wilhelm, R. S.//Kozlowski, J. A.B
  218358. TetrahedronC
  218359. ORGANOMETALLICS /COPPER /CuM
  218360. 17622N
  218361. 2/28/96V-The Chemistry of Higher Order Organocuprates.W
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  218364. GABRIEL WEATHERHEAD
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  218366. [A'Look, G. C.//Fotsch, C. H.//Wong, C. H.B
  218367. Acc. Chem. Res.M
  218368. 17623N
  218369. 2/28/96V|Enzyme-catalyzed organic synthesis: practical routes to aza sugars and their analogs for use as  glycoprocessing inhibitors.W
  218370. 1993X
  218371. 182-90Y
  218372. GABRIEL WEATHERHEAD
  218373. 16615
  218374. Long, J. R.B
  218375. Aldrichimica ActaC
  218376. OR ANOMETALLICS /LANTHANIDESM
  218377. 17624N
  218378. 2/28/96V!Lanthanides in Organic Synthesis.W
  218379. 1985X
  218380. GABRIEL WEATHERHEAD
  218381. 16616
  218382. Long, J. R.B
  218383. Aldrichimica ActaC
  218384. ORGANOMETALLICS /SILVER /AgM
  218385. 17625N
  218386. 2/28/96V/The Roles of Silver Salts in Organic Processes.W
  218387. 1981X
  218388. GABRIEL WEATHERHEAD
  218389. 16617
  218390. Lohray, B. B.B
  218391. Tetrahedron: AsymmetryM
  218392. 17626N
  218393. 2/28/96
  218394. ^V=Recent advances in the asymmetric dihydroxylation of alkenes.W
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  218396. 1317Y
  218397. GABRIEL WEATHERHEAD
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  218400. 17627N
  218401. 2/28/96V;Cyclic sulfites and cyclic sulfates: epoxide like  ynthons.W
  218402. 1992X
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  218404. GABRIEL WEATHERHEAD
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  218407. Angew. Chem., Int. Ed. Engl.C
  218408. 17628N
  218409. 2/28/96VDOxazaborolidines and dioxaborolidines in enantioselective catalysis.W
  218410. 1992X
  218411. GABRIEL WEATHERHEAD
  218412. 16620
  218413. Lockhoff, O.B
  218414. Angew. Chem., Int. Ed. Engl.M
  218415. 17629N
  218416. 2/28/96V9Glycolipids as immunomodulators-synthesis and properties.W
  218417. 1991X
  218418. 1611Y
  218419. GABRIEL WEATHERHEAD
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  218421. bA-Lloyd-Williams, P.//Albericio, F.//Giralt, E.B
  218422. TetrahedronM
  218423. 17630N
  218424. 2/28/96V)Convergent solid-phase peptide synthesis.W
  218425. 1993X    11065-133Y
  218426. GABRIEL WEATHERHEAD
  218427. 16622
  218428. Lloyd, D.//McNab, H.B
  218429. Adv.  eterocycl. Chem.M
  218430. 17631N
  218431. 2/28/96VA2,3-Dihydro-1,4-diazepines and 2,3-dihydro-1,4-diazepinium salts.W
  218432. GABRIEL WEATHERHEAD
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  218435. 17632N
  218436. 2/28/96V@Polarimetric detection in highperformance liquid chromatography.W
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  218438. GABRIEL WEATHERHEAD
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  218442. 17633N
  218443. 2/28/96V
  218444. Arsonium Ylides.W
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  218448. Luh, T.-Y.//Wong, K.-T.B    SynthesisC
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  218450. 2/28/96VTSilyl-substituted conjugated dienes: versatile building blocks of organic synthesis.W
  218451. 1993X
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  218453. GABRIEL WEATHERHEAD
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  218456. Acc. Chem. Res.C
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  218458. 2/28/96V=New synthetic applications of the dithioacetal functionality.W
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  218460. GABRIEL WEATHERHEAD
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  218463. 17636N
  218464. 2/28/96
  218465. hV6Transition-Metal-Mediated C-S Bond Cleavage Reactions.W
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  218467. GABRIEL WEATHERHEAD
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  218475. 17638N
  218476. 2/28/96V!Water-Promoted Organic-Reactions.W
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  218482. Chemtracts: Organic ChemistryM
  218483. 17639N
  218484. 2/28/96VhTargeting the DNA minor groove for control of biological function: progress, challenges, and  prospects.W
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  218492. 2/28/96VBDiscovery and development of anthracycline antitumour antibiotics.W
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  218498. Org. Prep. Proced. Int.C    OXI ATIONM
  218499. 17641N
  218500. 2/28/96VSRecent applications of oxochromiumamine complexes as oxidants in organic synthesis.W
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  218506. 17642N
  218507. 2/28/96V)Electrolysis of N-Heterocyclic Compounds.W
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  218512. Chem. Rev.C$REAGENTS /CCl3CHO /O=C-CCl3 /CHLORALM
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  218514. 2/28/96V
  218515. The Chemistry of Chloral.W
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  218519. Magnusson, G.B
  218520. Org. Prep. Proced. Int.C4FUNCTIONAL GROUPS /TRANSFORMATIONS /EPOXIDE CLEAVAGEM
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  218522. 2/28/96V7Rearrangements of  poxy alcohols and related compounds.W
  218523. 1990X
  218524. GABRIEL WEATHERHEAD
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  218527. TetrahedronC
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  218529. 2/28/96V
  218530. A general strategy using eta2-Co2(C0)6 acetylene complexes for the synthesis of the enediyne  antitumor agents esperamicin, calicheamicin, dynemicin and neocarzinostatin.W
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  218536. Acc. Chem. Res.
  218537. rCQC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /INDOLE ALKALOIDSM
  218538. 17646N
  218539. 2/28/96VMThe I dole-2,3-quinodimethane Strategy for the Synthesis of Indole Alkaloids.W
  218540. 1984X
  218541. GABRIEL WEATHERHEAD
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  218543. Magnus, P. D.B
  218544. TetrahedronCNFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C-X /SO2 /SULFONE /SM
  218545. 17647N
  218546. 2/28/96V)Recent Developments in Sulfone Chemistry.W
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  218549. GABRIEL WEATHERHEAD
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  218551. Magid, R. M.B
  218552. TetrahedronC_PHYSICAL ORGANIC /MECHANISMS /STEREOCHEMISTRY /REGIOCHEMISTRY /SN2' /NUCLEOPHILIC  SUBSTITUTIONM
  218553. 17648N
  218554. 2/28/96VhNucleophilic and Organometall c Displacement Reactions of Allylic Compounds: Stereo- and Regiochemistry.W
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  218560. Org. React. (N.Y.)ClFUNCTIONAL GROUPS /PREPARATIONS /O=C-H /ALDEHYDES /C-X /PR3 /C=PR3 /YLIDE  /KETONES /WITTIG /C=C /ALKENES /PM
  218561. 17649N
  218562. 2/28/96V
  218563. The Wittig Reaction.W
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  218565. GABRIEL WEATHERHEAD
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  218568. Tetra edronC
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  218570. 2/28/96V&Reduction of sulfoxides to thioethers.W
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  218573. GABRIEL WEATHERHEAD
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  218576. TetrahedronCkFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C-X /S /SULFIDES  /OXIDATION /C-X /SO /SULFOXIDESM
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  218578. 2/28/96V3Synthesis of Sulfoxides by Oxidation of Thioethers.W
  218579. 1986X
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  218581. GABRIEL WEATHERHEAD
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  218585. ORGANOMETALLICS /TITANIUM /FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /O=C-H  /O=C-R /KETONES /ALDEHYDES /ANNULATION /N-RING MACROCYCLISATION /PINACOL COUPLING /Ti  /DIOLS /C=C /ALKENESM
  218586. 17652N
  218587. 2/28/96V6Carbonyl-Coupling Reactions Using Low-Valent Titanium.W
  218588. 1989X
  218589. 1513Y
  218590. GABRIEL WEATHERHEAD
  218591. 16644
  218592. yA    Malek, J.B
  218593. Org. React. (N.Y.)
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  218595. 17653N
  218596. 2/28/96V
  218597. Reductions by Metal Alkoxyaluminum Hydrides. Part II. Carboxylic Acids and D rivatives, Nitrogen Compounds, and Sulfur Compounds.W
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  218599. GABRIEL WEATHERHEAD
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  218602. Org. React. (N.Y.)C_FUNCTIONAL GROUPS /METAL HYDRIDE /ALKOXYALUMINIUM HYDRIDES /LiAlH(OR)3  /LiAlH2(OR)2 /REDUCTIONM
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  218604. 2/28/96V+Reduction by Metal Alkoxyaluminum Hydrides.W
  218605. 1985X
  218606. GABRIEL WEATHERHEAD
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  218608. Malek, J.//Ce ny, M.B    SynthesisCBFUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDE /ALKOXYALUMINOHYDRIDESM
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  218610. 2/28/96V8Reduction of Organic Compounds by Alkoxyaluminohydrides.W
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  218612. GABRIEL WEATHERHEAD
  218613. 16647
  218614. Makosza, M.B    Synthesis
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  218617. 2/28/96V[Vicarious nucleophilic substitution of hydrogen in the chemistry of heterocyclic compounds.W
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  218619. GABRIEL WEATHERHEAD
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  218621. Makosza, M.//Fedorynski, M.B
  218622. Adv. Catal.CUODDS AND ENDS /TECHNIQUES AND METHODS /PHASE TRANSFER /PHASE TRANSFER CATALYSID  /PTCM
  218623. 17657N
  218624. 2/28/96VECatalysis in Two-Phase Systems. Phase Transfer and Related Phenomena.W
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  218626. GABRIEL WEATHERHEAD
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  218628. Makin, S. M.B
  218629. Pure Appl. Chem.CzTARGET SYNTHESIS /TERPENOIDS /FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /C=C-X(Y)  /O(O) /ENOL ETHERS /POLYENES /C=C-X-R /OM
  218630. 17658N
  218631. 2/28/96V%The Enol Ether Synthesis of Polyenes.W
  218632. 1976X
  218633. GABRIEL WEATHERHEAD
  218634. 16650
  218635. A*Majoral, J. P.//Badri, M.//Caminade, A. M.B
  218636. Heteroatom ChemistryM
  218637. 17659N
  218638. 2/28/96VCPolyazaphosphorus macrocycles: synthesis, reactivity, complexation.W
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  218640. GABRIEL WEATHERHEAD
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  218643. Pure Appl. Chem.M
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  218645. 2/28/96VgUnusual molecules-unusual reactions: from tetra-tert-butyltetrahedrane to the dimer of carbon  sulfide.W
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  218647. GABRIEL WEATHERHEAD
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  218650. Pure Appl. Chem.CbPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULES /SILABENZENE  /CYCLOPROPANYLIDENE /SiM
  218651. 17661N
  218652. 2/28/96V'From Silabenzene to Cyclopropanylidene.W
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  218654. GABRIEL WEATHERHEAD
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  218657. Angew. Chem., Int. Ed. Engl.C1TARGET SYNTHESIS /UNNATURAL PRODUCTS /CARBRIN  /4M
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  218659. 2/28/96V
  218660. The Cyclobutadiene Problem.W
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  218667. 2/28/96V
  218668. Carbalkoxycarbenes.W
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  218670. GABRIEL WEATHERHEAD
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  218673. Org. Prep. Pr ced. Int.M
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  218675. 2/28/96V1The use of isocyanides in heterocyclic synthesis.W
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  218677. GABRIEL WEATHERHEAD
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  218680. Pure Appl. Chem.M
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  218682. 2/28/96VBBiomimetic catalysts for selective oxidation in organic chemistry.W
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  218684. GABRIEL WEATHERHEAD
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  218689. 2/28/96V#The Skraup Synthesis of Quinolines.W
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  218693. Mann, J.B
  218694. Chem. Soc. Rev.CAFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /C-X /F /FLUORIDESM
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  218697. Modern Methods for the Introduction of Fluorine into Organic Molecules. An Approach to Compounds  with Altered Chemical and Biological Activities.W
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  218699. GABRIEL WEATHERHEAD
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  218701. Mann, J.B
  218702. Tetrahe ronCVPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS  /CYCLOADDITIONM
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  218704. 2/28/96V*The Synthetic Utility of Oxyallyl Cations.W
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  218707. GABRIEL WEATHERHEAD
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  218711. TARGET SYNTHESIS /MISCELLANEOUS /HETEROCYCLES /
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  218714. 2/28/96V^Conversion of 
  218715. -Lactams to Versatile Synthons via Molecular Rearrangement and Lactam Cleavage.W
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  218721. Adv. Phys. Org. Chem.C8PHYSICAL ORGANIC /ME HANISMS /ANNULATION /INTRAMOLECULARM
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  218723. 2/28/96V,Intramolecular Reactions of Chain Molecules.W
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  218730. 2/28/96V+The chemistry of gibberellins: an overview.W
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  218737. 2/28/96VNExploitation of Aryl Synthons in the Synthesis of Polycyclic Natural Products.W
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  218753. GABRIEL WEATHERHEAD
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  218771. 2/28/96V#Progress in Hydroazulene Synthesis.W
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  218777. 2/28/96V+Diene Synthesis via Boronate Fragmentation.W
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  218806. 2/28/96V7X-Ray structural analyses of organomagnesium compounds.W
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  218826. 2/28/96V=Synthetic aspects of the chemistry of p, -unsaturated amines.W
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  218833. 2/28/96V@Polycyclic Cage Compounds as Intermediates in Organic Synthesis.W
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  218841. 2/28/96VLSynthesis and Chemistry of Homocubanes, Bishomocubanes, and Trishomocubanes.W
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  218846. Martin, A. R.//Yang, Y.B
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  218858. 2/28/96VKUses of the Fries rearrangement for the preparation of hydroxyaryl ketones.W
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  218873. 2/28/96V.Recent advances in o-quinodimet ane chemistry.W
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  218911. Modern separation methods.W
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  218918. 2/28/96V[Reactions of carbonyl compounds with (monohalo) methyleniminium salts (Vilsmeier reagents).W
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  218921. GABRIEL WEATHERHEAD
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  218926. 2/28/96VeChiral alkoxyallylic and allenic stannanes as reagents for diastereo- and enantioselective synthesis.W
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  218933. 2/28/96V9SN2' Additions of Organocopper Reagents to Vinyloxiranes.W
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  218941. 2/28/96V\Trans-Cycloalkenes and [a.b]-Betweenanenes, Molecular Jump Ropes and Double Bond Sandwiches.W
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  218948. 2/28/96V4Noncovalent design principles and the new synthesis.W
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  218971. 2/28/96VBAdvances in Stereochemical Control: The 1,2- and 1,3-Diol Systems.W
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  218978. 2/28/96V'Recent Progress in Macrolide Synthesis.W
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  219001. The Wittig Olefination and Modifications Involving Phosphoryl-Stabilised Carbanions.  Stereochemistry, Mechanism, and Selected Synthetic Aspects.W
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  219003. GABRIEL WEATHERHEAD
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  219005. Marvell, E. N.//Li, T.B    SynthesisCrFUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENATION /C=C /ALKYNES /RE UCTION /SEMIHYDROGENATION /C=C /ALKENES /ZM
  219006. 17709N
  219007. 2/28/96V/Catalytic Semihydrogenation of the Triple Bond.W
  219008. 1973X
  219009. GABRIEL WEATHERHEAD
  219010. 16701
  219011. Maruyama, K.//Katagiri, T.B%Journal of Physical Organic ChemistryC
  219012. ORGANOMETALLICS /MAGNESIUM /MgM
  219013. 17710N
  219014. 2/28/96V#Mechanism of the Grignard reaction.W
  219015. 1989X
  219016. GABRIEL WEATHERHEAD
  219017. 16702
  219018. Maruoka, K.//Yamamoto, H.B
  219019. TetrahedronC
  219020. ORGANOMETALLICS /AlM
  219021. 17711N
  219022. 2/28/96V&Organoaluminiums in Organic Synthesis.W
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  219024. GABRIEL WEATHERHEAD
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  219026. A Martynov, I. V.//Yurtanov, A. I.B Russ. Chem. Rev. (Engl. Transl.)M
  219027. 17712N
  219028. 2/28/96V=alpha-Halo-alpha-nitrocarboxylic acids and their derivatives.W
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  219030. GABRIEL WEATHERHEAD
  219031. 16704
  219032. A'Martin, M. J.//Dorn, L. J.//Cook, J. M.M
  219033. 17713N
  219034. 2/28/96VqNovel pyridodiindoles, azadiindoles, and indolopyridoimidazoles via the Fischer-indole cyclization.  HeterocyclesW
  219035. 1993X
  219036. 157-89Y
  219037. GABRIEL WEATHERHEAD
  219038. 16705
  219039. Matsuura, T.//Omura, K.B    SynthesisCpC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /PHOTOCHEMICAL REACTIONS  /ARENES /HYDROXYLATION /Ar-X /OHM
  219040. 17714N
  219041. 2/28/96V2Photochemical Hydroxylation of Aromatic Compounds.W
  219042. 1974X
  219043. GABRIEL WEATHERHEAD
  219044. 16706
  219045. Matsumoto, K.//Sera, A.B    SynthesisC4ODDS AND ENDS /TECHNIQUES AND METHODS /HIGH PRESSUREM
  219046. 17715N
  219047. 2/28/96V.Organic Synthesis Under High Pressure, Part I.W
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  219049. GABRIEL WEATHERHEAD
  219050. 16707
  219051. Mathias, J. P.//Stoddart, J. F.B
  219052. Top. Curr. Chem.M
  219053. 17716N
  219054. 2/28/96V
  219055. Substrate-directed synthesis: the rapid assembly of novel macropolycyclic structures via  stereoregular Diels-Alder oligomerization.W
  219056. 1993X
  219057. 1-69Y
  219058. GABRIEL WEATHERHEAD
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  219060. Mathias, J. P.//Stoddart, J.B
  219061. Chem. Soc. Rev.M
  219062. 17717N
  219063. 2/28/96V"Constructing a molecular LEGO set.W
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  219065. GABRIEL WEATHERHEAD
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  219067. Mathias, L. J.B    SynthesisCTFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /ISOUREAS /ESTERIFICATION  ALKYLATIONM
  219068. 17718N
  219069. 2/28/96V;Esterification and Alkylation Reactions Employing Isoureas.W
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  219071. GABRIEL WEATHERHEAD
  219072. 16710
  219073. A&Mathey, F.//Marinetti, A.//Mercier, F.B
  219074. SynlettC
  219075. 17719N
  219076. 2/28/96VvSynthesis of organophospho us compounds via the coordination spheres of transition metals: some nonclassical examples.W
  219077. 1992X
  219078. GABRIEL WEATHERHEAD
  219079. 16711
  219080. Mathey, F.B
  219081. Acc. Chem. Res.C
  219082. 17720N
  219083. 2/28/96
  219084. VOExpanding the analogy between phosphorus-carbon and carbon-carbon double bonds.W
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  219086. GABRIEL WEATHERHEAD
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  219088. Mathey, F.B
  219089. Chem. Rev.C
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  219091. 2/28/96V7Chemistry  f 3-membered carbon-phosphorus heterocycles.W
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  219093. GABRIEL WEATHERHEAD
  219094. 16713
  219095. Mataga, N.B
  219096. Pure Appl. Chem.M
  219097. 17722N
  219098. 2/28/96V>Photoinduced electron transfer and multiple states mechanisms.W
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  219100. 1605-10Y
  219101. GABRIEL WEATHERHEAD
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  219104. 17723N
  219105. 2/28/96V$En lization of the phosphoryl group.W
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  219108. GABRIEL WEATHERHEAD
  219109. 16715
  219110. Mastryukova, T. A.B
  219111. Heteroatom ChemistryC
  219112. 17724N
  219113. 2/28/96V:Some aminophosphinocarboxylic acids and their derivatives.W
  219114. 1991X
  219115. GABRIEL WEATHERHEAD
  219116. 16716
  219117. Massey, A. G.//Humphries, R. E.B
  219118. Aldrichimica ActaM
  219119. 17725N
  219120. 2/28/96V@The direct synthesis of non-transition-metal organo derivatives.W
  219121. 1989X
  219122. GABRIEL WEATHERHEAD
  219123. 16717
  219124. Mason, S. F.B    ChiralityM
  219125. 17726N
  219126. 2/28/96V5The development of concepts of chiral discrimination.W
  219127. 1989X
  219128. GABRIEL WEATHERHEAD
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  219130. Mashkina, A. V.B
  219131. Sulfur ReportsC
  219132. 17727N
  219133. 2/28/96V9Catalytic synthesis of sulfides, sulfoxides and sulfones.W
  219134. 1991X
  219135. GABRIEL WEATHERHEAD
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  219137. Mascaretti, O. A.B
  219138. Aldrichimica ActaC
  219139. 17728N
  219140. 2/28/96VGModern methods for the monofluorination of aliphatic organic compounds.W
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  219142. 47-58Y
  219143. GABRIEL WEATHERHEAD
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  219145. A"McClinton, M. A.//McClinton, D. A.B
  219146. TetrahedronC
  219147. 17729N
  219148. 2/28/96VATrifluoromethylations and related reactions in organic chemistry.W
  219149. 1992X
  219150. 6555Y
  219151. GABRIEL WEATHERHEAD
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  219153. Mazzucato, U.//Momicchioli, F.B
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  219156. 2/28/96V2Rotational isomerism in trans-1,2-diarylethylenes.W
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  219159. GABRIEL WEATHERHEAD
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  219161. Mayr, H.//Patz, M.B
  219162. Angew. Chem., Int. Ed. Engl.M
  219163. 17731
  219164. 2/28/96VrScales Of Nucleophilicity And Electrophilicity - A System For Ordering  Polar  rganic And Organometallic ReactionsW
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  219167. GABRIEL WEATHERHEAD
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  219170. Gazz. Chim. Ital.M
  219171. 17732N
  219172. 2/28/96Vp3,3,4,4,5,5-Hexamethyl-1,2-bis(methylene)cyclopentane: a novel probe for the study of  cycloaddition mechanisms.W
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  219174. GABRIEL WEATHERHEAD
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  219177. Adv. Organomet. Chem.M
  219178. 17733N
  219179. 2/28/96V>Recent advances in the chemistry of metal-carbon triple bonds.W
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  219181. GABRIEL WEATHERHEAD
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  219183. Mayr, H.B
  219184. Angew. Chem., Int. Ed. Engl.M
  219185. 17734N
  219186. 2/28/96V^Carbon-carbon bond formation by addition of carbenium ions to alkenes: Kinetics and mechanism.W
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  219194. 2/28/96VNStereochemical Control Of Transition-Metal Complexes By Polyphosphine  LigandsW
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  219196. GABRIEL WEATHERHEAD
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  219198. A1Matveev, Y. I.//Gorbatenko, V. I.//Samarai, L. I.B
  219199. TetrahedronM
  219200. 17736N
  219201. 2/28/96V91,1-Dihaloalkyl heterocumulenes: synthesis and reactions.W
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  219204. GABRIEL WEATHERHEAD
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  219206. Matteson, D. S.B
  219207. TetrahedronC
  219208. 17737N
  219209. 2/28/96V+Boronic esters in stereodirected synthesis.W
  219210. 1989X
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  219212. GABRIEL WEATHERHEAD
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  219215. Chem. Rev.CfC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /BORON /STEREOCHEMISTRY  /HALOBORONIC ESTERS /BM
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  219217. 2/28/96VEalpha-Haloboronic Esters: Intermediates for Stereodirected Synthesis.W
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  219220. GABRIEL WEATHERHEAD
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  219224. 17739N
  219225. 2/28/96V5The Use of Chiral Organoboranes in Organic Synthesis.W
  219226. 1986X
  219227. GABRIEL WEATHERHEAD
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  219229. McMurry, J. E.B
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  219232. 2/28/96
  219233. V)Organic Chemistry of Low-Valent Titanium.W
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  219235. GABRIEL WEATHERHEAD
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  219238. Acc. Chem. Res.M
  219239. 17741N
  219240. 2/28/96V<Three-center, two-electron C-H-C bonds in organic chemistry.W
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  219242. GABRIEL WEATHERHEAD
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  219244. McKillop, A.//Young, D. W.B    SynthesisC9ODDS AND ENDS /TECHNIQUES AND METHODS /SUPPORTE  REAGENTSM
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  219246. 2/28/96V+Organic Synthesis Using Supported Reagents.W
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  219248. GABRIEL WEATHERHEAD
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  219250. McKervey, A.//Bohmer, V.B    Chem. Br.M
  219251. 17743N
  219252. 2/28/96V$Calixarenes-supramolecular pursuits.W
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  219254. GABRIEL WEATHERHEAD
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  219259. 2/28/96V>Some recent synthetic routes to thioketones and thioaldehydes.W
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  219262. GABRIEL WEATHERHEAD
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  219264. A!McGovern, P.//Vollhardt, K. P. C.B
  219265. SynlettM
  219266. 17745N
  219267. 2/28/96
  219268. VZThe Synthesis and Novel Reactivity of Homo- and Heterodinuclear Fulvalene Metal Carbonyls.W
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  219270. GABRIEL WEATHERHEAD
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  219273. Adv. Organomet. Chem.C
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  219275. 2/28/96VUSlowed tripodal rotation in arene-chromium complexes: steric and electronic barriers.W
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  219277. GABRIEL WEATHERHEAD
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  219279. McGill, C. K.//Rappa, A.B
  219280. Adv. Heterocycl. Chem.C
  219281. NAME REACTIONSM
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  219283. 2/28/96V%Advances in the Chichibabin reaction.W
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  219285. GABRIEL WEATHERHEAD
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  219287. McElvain, S. M.B
  219288. Org. React. (N.Y.)M
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  219290. 2/28/96V
  219291. The Acyloins.W
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  219293. GABRIEL WEATHERHEAD
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  219295. McDonald, R. N.B
  219296. TetrahedronC[PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICAL IONS /CARBENOIDS /CARBENE ANION  RADICALSM
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  219298. 2/28/96VYGeneration, Thermochemistry, and Chemistry of Carbene Anion Radicals and Related Species.W
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  219301. GABRIEL WEATHERHEAD
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  219303. A.McDaniel, C. W.//Bradshaw, J. S.//Izatt, R. M.B
  219304. HeterocyclesM
  219305. 17750N
  219306. 2/28/96V.Proton-ionizable crown ethers. A short review.W
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  219308. GABRIEL WEATHERHEAD
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  219310. A3McCombie, S. W.//Ortiz, C.//Cox, B.//Ganguly, A. K.B
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  219314. 1993  Controlling benzylic and anomeric functionality and stereochemistry: methodology and syntheses  utilizing intramolecular ionic hydrogenation.X
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  219319. Angew. Chem., Int. Ed. Engl.C
  219320. PHYSICAL ORGANIC /REARRANGEMENTS /ALPHA DIAZOCARBONYL X=Y=Z /C,N,N /DIAZAKETONES  /WOLFF REARRANGEMENT /KETENES /X=Y=Z /C,C,O /ESTERSM
  219321. 17752N
  219322. 2/28/96V9The Wolff Rearrangement of alpha-Diazocarbonyl Compounds.W
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  219324. GABRIEL WEATHERHEAD
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  219326. A    Meier, H.B    SynthesisCHC-C BOND FORMATION /ANNULATIONS /MEDIUM RING /ALKYNES /CYCLOALKYNES /C=CM
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  219328. 2/28/96V&Synthesis of Medium Ring Cycloalkynes.W
  219329. 1972X
  219330. GABRIEL WEATHERHEAD
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  219335. 2/28/96VgRecent Advances In The Chemistry Of Homometallic And Heterometallic  Alkoxides Of P-Block  Metal(loid)sW
  219336. 1994X    1643-1660Y
  219337. GABRIEL WEATHERHEAD
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  219339. McQuillin, F. J.B
  219340. Progress in Organic ChemistryCVFUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENATION /REDUCTION /HOMOGENEOUS /Co  /RhM
  219341. 17755N
  219342. 2/28/96V&Homogeneously Catalysed Hydrogenation.W
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  219344. GABRIEL WEATHERHEAD
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  219346. McPherson, M. J.//H., Parish J.B
  219347. Nat. Prod. Rep.M
  219348. 17756N
  219349. 2/28/96V8Chemical and biochemical manipulations of nucieic acids.W
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  219352. GABRIEL WEATHERHEAD
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  219354. A!McOmie, J. F. W.//Blatchly, J. M.B
  219355. Org. React. (N.Y.)C+NAME REACTIONS /THIELE-WINTER ACETOXY ATIONM
  219356. 17757N
  219357. 2/28/96V,The Thiele-Winter Acetoxylation of Quinones.W
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  219359. GABRIEL WEATHERHEAD
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  219361. A,McMurry, T. J.//Raymond, K. N.//Smith, P. H.B
  219362. ScienceM
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  219365. V7Molecular recognition and metal ion template synthesis.W
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  219367. GABRIEL WEATHERHEAD
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  219369. McMurry, J. E.B
  219370. Org. React. (N.Y.)C
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  219372. 17759N
  219373. 2/28/96V*Ester Cleavages via SN2-Type Dealkylation.W
  219374. 1976X
  219375. GABRIEL WEATHERHEAD
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  219378. HeterocyclesM
  219379. 17760N
  219380. 2/28/96VtThe synthesis of pyridines, quinolines and other related systems by the Vilsmeier and the reverse  Vilsmeier method.W
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  219383. GABRIEL WEATHERHEAD
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  219385. Meth-Cohn, O.B
  219386. Acc. Chem. Res.C2PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /NITRENESM
  219387. 17761N
  219388. 2/28/96V2New Synthetic Applications of Oxycarbonylnitrenes.W
  219389. 1987X
  219390. GABRIEL WEATHERHEAD
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  219392. Meskens, F. A. J.B    Synthesis
  219393. FUNCTIONAL GRO PS /PREPARATIONS /ETHERS /HETRING /3(O) /EPOXIDES /OXIRANES /C-X /OH /ALCOHOLS /O=C-H  /ALDEHYDES /O=C-R /KETONES /ACETALISATION /ACETALS /C-X(Y) /O(O)M
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  219395. 2/28/96VXMethods for the Preparation of Acetals from Alcohols or Oxiranes and Carbonyl Compounds.W
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  219397. GABRIEL WEATHERHEAD
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  219400. Nat. Prod. Rep.M
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  219402. 2/28/96V
  219403. Clerodane diterpenoids.W
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  219405. GABRIEL WEATHERHEAD
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  219407. Merkushev, E. B.B    SynthesisCGFUNCTIONAL GROUPS /TRANSFORMATIONS /Ar-X TO Ar-Y /Ar-X /N2 /Ar-X /I /TlM
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  219409. 2/28/96V4Advances in the Synthesis of Iodoaromatic Compounds.W
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  219411. GABRIEL WEATHERHEAD
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  219414. Acc. Chem. Res.C2PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALSM
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  219416. 2/28/96V
  219417. The Captodative Effect.W
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  219419. GABRIEL WEATHERHEAD
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  219422. Acc. Chem. Res.M
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  219424. 2/28/96V.Enzyme reactivity from an organic perspective.
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  219427. GABRIEL WEATHERHEAD
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  219429. Meng, Q.//Hesse, M.B
  219430. Top. Curr. Chem.M
  219431. 17767N
  219432. 2/28/96VERing Closure Methods in the Synthesis of Macrocyclic Natural ProductsW
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  219434. GABRIEL WEATHERHEAD
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  219438. 2/28/96V=Spiro[2.4]hepta-4,6-dienes: Synthesis and Chemical Reactions.W
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  219440. GABRIEL WEATHERHEAD
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  219445. 2/28/96VKRelative Reactivities of C-C Double and Triple Bonds Towards Electrophiles.W
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  219452. 2/28/96V_The borylation of aromatic compounds by dehalogenation products of (dialkylamino)dihaloboranes.W
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  219474. 2/28/96V[Dendrimers, arborols and cascade molecules: breakthrough into generations of new materials.W
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  219480. Angew. Chem., Int. Ed. Engl.CKFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /HETRING /5(N,O) /OXAZOLINESM
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  219482. 2/28/96V&The Synthetic Utility of 2-Oxazolines.W
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  219484. GABRIEL WEATHERHEAD
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  219487. New Journal of ChemistryM
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  219498. 2/28/96V\Metalloporphyrins as versatile catalysts for oxidation reactions and oxidative DNA cleavage.W
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  219505. 2/28/96VJThe use of thiocarbonyl compounds in carbon-carbon bond forming reactions.W
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  219513. 2/28/96VHIntramolecular Oxidative Cyclisation of Alcohols with Lead Tetraacetate.W
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  219519. 2/28/96VNLevoglucosenone: The Properties, Reactions, and Use in Fine Organic Synthesis.W
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  219534. 2/28/96VeA medicinal chemistry case study: An account of an angiotensin II antagonist drug d scovery programmeW
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  219545. GABRIEL WEATHERHEAD
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  219559. 2/28/96V)Indolizidine and quinolizidine alkaloids.W
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  219567. 2/28/96V/Quinoline, quinazoline, and acridone alkaloids.W
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  219628. 2/28/96VcElectron-Transfer Processes: Peroxydisulfate, A Useful and Versatile Reagent in Organic  Chemistry.W
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  219654. 2/28/96VCSteroidal oligoglycosides and polyhydroxysteroids from Echinoderms.W
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  219706. 2/28/96VAAcyclic stereocontrol via [2,3]-Wittig sigmatropic rearrangement.W
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  219765. 2/28/96V5The Chemistry of Peroxonium Ions and Dioxygen Ylides.W
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  219792. 2/28/96V'Organosilicon synthesis of isocyanates.W
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  219823. 2/28/96VPMarine pyridoacridine alkaloids: structure, synthesis, and biological chemistry.W
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  219830. 2/28/96VeIminophosphoranes - Useful Building-Blocks For The Preparation Of  Nitrogen-Containing  Heterocycles.W
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  219867. 1994X
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  219869. GABRIEL WEATHERHEAD
  219870. 16818
  219871. 'A:Mohiuddin, G.//Satyanarayana, P.//Ahmed, K.//Ratnam, C. V.B
  219872. HeterocyclesC6C-C BOND FORMATION /HETEROANNULATIONS /BENZODIAZEPINESM
  219873. 17827N
  219874. 2/28/96VBRecent Advances in the Synthesis of Annelated 1,4-Benzodiazepines.W
  219875. 1986X
  219876. 3489Y
  219877. GABRIEL WEATHERHEAD
  219878. 16819
  219879. Moderhack, D.B
  219880. J. Heterocycl. Chem.M
  219881. 17828N
  219882. 2/28/96V<Oxo- and imino-functionalized 1,2-oxazetidines. An overview.W
  219883. 1993X
  219884. 579-91Y
  219885. GABRIEL WEATHERHEAD
  219886. 16820
  219887. Moderhack, D.B    SynthesisCeC-C BOND FORMATION /ANNULATIONS /4-RING /CYCLOPROPANES CYCLOPROPENES /[1+1+2]  /CYCLOADDITIONS /[1+3]M
  219888. 17829N
  219889. 2/28/96V5Four-Membered Rings from Isocyanides-Recent Advances.W
  219890. 1985X
  219891. 1083a
  219892. GABRIEL WEATHERHEAD
  219893. 16821
  219894. Moriarty, R. M.//Prakash, O.B
  219895. Acc.  hem. Res.C REAGENTS /SOLVENTS /CATALYSTS /IM
  219896. 17830N
  219897. 2/28/96V(Hypervalent Iodine in Organic Synthesis.W
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  219899. GABRIEL WEATHERHEAD
  219900. 16822
  219901. Moriarty, R. M.B
  219902. Top. Stereochem.C.PHYSICAL ORGANIC /STEREOCHEMISTRY /CARBRING /4
  219903. 17831N
  219904. 2/28/96V<The Stereochemistry of Cyclobutane and Heterocyclic Analogs.W
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  219906. GABRIEL WEATHERHEAD
  219907. 16823
  219908. Mori, K.B
  219909. TetrahedronC
  219910. TARGET SYNTHESIS /PHEROMONEM
  219911. 17832N
  219912. 2/28/96V)Synthesis of Optically Active Pheromones.W
  219913. 1989X
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  219915. GABRIEL WEATHERHEAD
  219916. 16824
  219917. Mori, K.//Watanabe, H.B
  219918. Pure Appl. Chem.M
  219919. 17833N
  219920. 2/28/96VQRecent results in the synthesis of semiochemicals: synthesis of glycinoeclepin A.W
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  219922. GABRIEL WEATHERHEAD
  219923. 16825
  219924. Mori, K.B
  219925. Chem. Scr.M
  219926. 17834N
  219927. 2/28/96VKSynthesis as an indispensable tool for the study of chemical communication.W
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  219929. GABRIEL WEATHERHEAD
  219930. 16826
  219931. Moreno-Manas, M.//Pleixatz, R.B
  219932. Adv. Heterocycl. Chem.M
  219933. 17835N
  219934. 2/28/96V@Dehydroacetic acid, triacetic acid lactone, and related pyrones.W
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  219936. GABRIEL WEATHERHEAD
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  219938. Moore, H. W.//Yerxa, B. R.B
  219939. Chemtracts: Organic ChemistryM
  219940. 17836N
  219941. 2/28/96
  219942. 0V4Ring expansions of cyclobutenones-synthetic utility.W
  219943. 1992X
  219944. GABRIEL WEATHERHEAD
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  219946. Moore, H. W.//Gheorghina, M. D.B
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  219949. 17837N
  219950. 2/28/96V+Cyanoketenes: Synthesis and Cycloadditions.W
  219951. 1981X
  219952. GABRIEL WEATHERHEAD
  219953. 16829
  219954. Moore, M. L.B
  219955. Org. React. (N.Y.)M
  219956. 17838N
  219957. 2/28/96V
  219958. The Leuckart Reaction.W
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  219960. GABRIEL WEATHERHEAD
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  219962. Moody, C. J.B
  219963. SynlettM
  219964. 17839N
  219965. 2/28/96V!Synthesis Of Carbazole Alkaloids.W
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  219968. GABRIEL WEATHERHEAD
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  219971. Chem. Ind. (London)M
  219972. 17840N
  219973. 2/28/96V
  219974. Fullerene chemistry.W
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  219981. 2/28/96
  219982. 5V1Claisen Rearrangeme ts in Heteroaromatic Systems.W
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  219984. GABRIEL WEATHERHEAD
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  219987. Acc. Chem. Res.C>PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /CARBENESM
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  219992. GABRIEL WEATHERHEAD
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  219995. Acc. Chem. Res.C
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  219998. 2/28/96V3Carbenic Selectivity in Cyclopropanation Reactions.W
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  220005. 2/28/96V1The Synthesis of Aldehydes from Carboxylic Acids.W
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  220007. GABRIEL WEATHERHEAD
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  220012. 2/28/96V7The Rosenmund Reduction of Acid Chlorides to Aldehydes.W
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  220033. 2/28/96V$Asymmetric Homogenous Hydrogenation.W
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  220035. GABRIEL WEATHERHEAD
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  220043. Moritani, I.//Fujiwara, Y.B    SynthesisC_C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE /ORGANOMETALLICS /PALLADIUM  /ARENES /C=C-Ar /PdM
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  220097. 2/28/96V%Azlactones : Retrospect and Prospect.W
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  220117. 16851
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  220120. 17860N
  220121. 2/28/96V#Control of Acyclic Stereochemistry.W
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  220129. 2/28/96V
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  220141. GABRIEL WEATHERHEAD
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  220151. 2/28/96V*Cross-Coupling Reactions Based on Acetals.W
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  220159. 2/28/96V-Catalytic Reduction of Aromatic Hydrocarbons.W
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  220175. 2/28/96V=Photocycloadditions: control by energy and electron transfer.W
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  220189. 2/28/96V=Electrocatalytic hydrogenation on hydrogen-active electrodes.W
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  220196. 2/28/96VPSynthesis Of Carcinogenic Oxygenated Derivatives Of B nz[c]acridines -  A ReviewW
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  220203. 2/28/96V+Synthesis of carcinogenic benz[c]acridines.W
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  220206. GABRIEL WEATHERHEAD
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  220211. 2/28/96V1The role of zinc carbenoids in organic synthesis.W
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  220213. GABRIEL WEATHERHEAD
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  220216. Chemtracts: Organic ChemistryM
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  220218. 2/28/96V`Angiotensin II receptor antagonists: the next step in the evolution of antihypertensive therapy.W
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  220224. 17874N
  220225. 2/28/96V$Naturally occurring plant coumarins.W
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  220227. GABRIEL WEATHERHEAD
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  220229. Murray, R. W.B
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  220233. 2/28/96V
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  220237. GABRIEL WEATHERHEAD
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  220243. 2/28/96VYThe Wittig Olefination Reaction with Carbonyl Compounds Other Than Aldehydes and Ketones.W
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  220250. 2/28/96V5Siloxycyclopropanes - useful synthetic intermediates.W
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  220252. GABRIEL WEATHERHEAD
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  220255. Chemtracts: Organic ChemistryC
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  220257. 2/28/96VSLow-Valent Ruthenium Complexes as Lewis Acids Catalysts for Activa ion of Nitriles.W
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  220260. GABRIEL WEATHERHEAD
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  220262. Murahashi, S.B
  220263. Pure Appl. Chem.C
  220264. 17879N
  220265. 2/28/96VKBiomimetic oxidation in organic synthesis using transition metal catalysts.W
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  220267. GABRIEL WEATHERHEAD
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  220269. Muller, H.-M.//Seebach, D.B
  220270. Angew. Chem., Int. Ed. Engl.M
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  220272. 2/28/96VXPoly(hydroxybutanoates): A fifth class of physiologically important organic biopolymers.W
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  220275. GABRIEL WEATHERHEAD
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  220279. 2/28/96VhThe Diyne Reaction of 1,4-, 1,5-, 1,6-, and 1,7-Diynes via Transition Metal Complexes to New  Compounds.W
  220280. 1974X
  220281. GABRIEL WEATHERHEAD
  220282. 16873
  220283. Muller, W. H.B
  220284. Angew. Chem., Int. Ed. Engl.CLFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /THIIRANIUM IONS /SM
  220285. 17882N
  220286. 2/28/96V*Thiiranium Ions as Reaction Intermediates.W
  220287. 1969X
  220288. GABRIEL WEATHERHEAD
  220289. 16874
  220290. Nagahara, T.//Kametani, T.B
  220291. Heterocycles
  220292. C-C BOND FORMATION /HETEROANNULATIONS /4-RING /STEREOCHEMISTRY /ENANTIOGENIC  /AMINO ACIDS /BUTYROLACTONE  D-GLUCOSAMINE /D-GLUCOSE /CEPHALOSPORINS /ENANTIOSELECTIVE /CARBAPENEM ANTIBIOTICSM
  220293. 17883N
  220294. 2/28/96V5Enantioselective Synthesis of Carbapenem Antibiotics.W
  220295. 1987X
  220296. GABRIEL WEATHERHEAD
  220297. 16875
  220298. `A@Naddaka, V. I.//Sadekov, I. D.//Maksimenko, A. A.//Minkin, V. I.B
  220299. Sulfur ReportsC
  220300. 17884N
  220301. 2/28/96V2 -Telluranes: synthesis, structure and reactivity.W
  220302. 1988X
  220303. GABRIEL WEATHERHEAD
  220304. 16876
  220305. Nace, H. R.B
  220306. Org. React. (N.Y.)C
  220307. 17885N
  220308. 2/28/96VOThe Preparation of Olefins by the Pyrolysis of Xanthates: The Chugaev Reaction.W
  220309. 1962X
  220310. GABRIEL WEATHERHEAD
  220311. 16877
  220312. Na ata, W.//Yoshioka, M.B
  220313. Org. React. (N.Y.)CaC-C BOND FORMATION /APPENDAGES /1,4-ADDITION /O=C-C=C /KETONES /ENONES  /HYDROCYANATION /NITRILESM
  220314. 17886N
  220315. 2/28/96V/Hydrocyanation of Conjugate Carbonyl Compounds.W
  220316. 1977X
  220317. GABRIEL WEATHERHEAD
  220318. 16878
  220319. Muzart, J.B    SynthesisC
  220320. 17887N
  220321. 2/28/96VySilyl ethers as protective groups for alcohols: oxidative deprotection and stability under alcohol  oxidation conditions.W
  220322. 1993X
  220323. GABRIEL WEATHERHEAD
  220324. 16879
  220325. Muzart, J.B
  220326. Chem. Rev.C
  220327. OXIDATION /CrM
  220328. 17888N
  220329. 2/28/96V3Chromium-catalyzed oxidations in organic synthesis.W
  220330. 1992X
  220331. GABRIEL WEATHERHEAD
  220332. 16880
  220333. Mutter, M.//Vuilleumier, S.B
  220334. Angew. Chem., Int. Ed. Engl.M
  220335. 17889N
  220336. 2/28/96VWA chemical approach to protein synthesis: Template-assem led synthetic proteins (TASP).W
  220337. 1989X
  220338. GABRIEL WEATHERHEAD
  220339. 16881
  220340. Narayana, C.//Periasamy, M.B    SynthesisC-ORGANOMETALLICS /SYNTHESIS /CO /CARBONYLATIONM
  220341. 17890N
  220342. 2/28/96VTOrganic Synthesis via Carbonylation of Organometallic Reagents with Carbon Monoxide.W
  220343. 1985X
  220344. GABRIEL WEATHERHEAD
  220345. 16882
  220346. Narasimhan, N. S.//Mali, R. S.B    Synthesis
  220347. gCwC-C BOND FORMATION /HETEROANNULATIONS /MISCELLANEOUS /ORGANOMETAL ICS /LITHIUM /METALLATION,LITHIATION /HETEROCYCLE /LiM
  220348. 17891N
  220349. 2/28/96VRSyntheses of Heterocyclic Compounds Involving Aromatic Lithiation in the Key Step.W
  220350. 1983X
  220351. GABRIEL WEATHERHEAD
  220352. 16883
  220353. Narasaka, K.B
  220354. Pure Appl. Chem.M
  220355. 17892N
  220356. 2/28/96VAChiral reagents for asymmetric constructi n of carbon frameworks.W
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  220358. 1889Y
  220359. GABRIEL WEATHERHEAD
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  220361. Narasaka, K.B    SynthesisCiC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[2+2] /[4+2] /ENE  REACTIONS /B /Al /Sn /Ti /RuM
  220362. 17893N
  220363. 2/28/96V5Chiral Lewis acids in catalytic asymmetric reactions.W
  220364. 1991X
  220365. GABRIEL WEATHERHEAD
  220366. 16885
  220367. Nakazaki, M.B
  220368. Top. Stereochem.C$TARGET SYNTHESIS /UNNATURAL PRODUCTSM
  220369. 17894N
  220370. 2/28/96VQThe Synthesis and Stereochemistry of Chiral Organic Molecules with High Symmetry.W
  220371. 1984X
  220372. GABRIEL WEATHERHEAD
  220373. 16886
  220374. kA&Nakayama, J.//Konishi, T.//Hoshino, M.B
  220375. Heterocycles
  220376. HETEROCYCLESM
  220377. 17895N
  220378. 2/28/96V#Preparation of thiophene oligomers.W
  220379. 1988X
  220380. 1731Y
  220381. GABRIEL WEATHERHEAD
  220382. 16887
  220383. Nakasu i, K.B
  220384. Pure Appl. Chem.M
  220385. 17896N
  220386. 2/28/96V?New multi-stage redox systems and new organic molecular metals.W
  220387. 1990X
  220388. GABRIEL WEATHERHEAD
  220389. 16888
  220390. Nakamura, E.B
  220391. SynlettC
  220392. 17897N
  220393. 2/28/96V.New tools in synthetic organocopper chemistry.W
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  220395. GABRIEL WEATHERHEAD
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  220397. Nakai, T.//Mikami, K.B
  220398. Org. React. (N.Y.)M
  220399. 17898N
  220400. 2/28/96V
  220401. The [2,3]-Wittig Reaction.W
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  220404. GABRIEL WEATHERHEAD
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  220406. Nakai, T.//Mikami, K.B
  220407. Chem. Rev.C<C-C BOND FORMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[2,3]M
  220408. 17899N
  220409. 2/28/96V=[2,3]-Wittig Sigmatropic Rearrangements in Organic Synthesis.W
  220410. 1986X
  220411. GABRIEL WEATHERHEAD
  220412. 16891
  220413. Nagata, R.//Saito, I.B
  220414. SynlettM
  220415. 17900N
  220416. 2/28/96V0Selective Oxidations by Peroxid -Based Reagents.W
  220417. 1990X
  220418. GABRIEL WEATHERHEAD
  220419. 16892
  220420. Nagata, W.B
  220421. Pure Appl. Chem.M
  220422. 17901N
  220423. 2/28/96V{Contributions to the chemistry of 
  220424. -lactam antibiotics: 1-oxa nuclear analogs of naturally  occurring 
  220425. -lactam antibiotics.W
  220426. 1989X
  220427. GABRIEL WEATHERHEAD
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  220429. Nagai, T.//Hamaguchi, M.B
  220430. Org. Prep. Proced. Int.M
  220431. 17902N
  220432. 2/28/96VWRecent progress in the preparation and synthetic uses of the reactions of 3H-pyrazoles.W
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  220434. 403-35Y
  220435. GABRIEL WEATHERHEAD
  220436. 16894
  220437. Negishi, E.B
  220438. Acc. Chem. Res.C@ORGANOMETALLICS /ZIRCONIUM /C-X /Zr /ANNULATION CARBOMETALLATIONM
  220439. 17903N
  220440. 2/28/96VkControlled Carbometallation as a Tool for Carbon-Carbon Bond Formation and its Application to  Cyclisation.W
  220441. 1987X
  220442. GABRIEL WEATHERHEAD
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  220444. Negishi, E.//Idacavage, M. J.B
  220445. Org. React. (N.Y.)C
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  220447. 17904N
  220448. 2/28/96V[Formation of Carbon-Carbon and Carbon-Heteroatom Bonds via Organoboranes and Organoborates.W
  220449. 1985X
  220450. GABRIEL WEATHERHEAD
  220451. 16896
  220452. Negishi, E.-i.
  220453. Acc. Chem. Res.CFORGANOMETALLICS /NICKEL /PALLADIUM /COUPLING /ALKENES /ALKANES /Ni /PdM
  220454. 17905N
  220455. 2/28/96V]Palladium- or Nickel-Catalysed Cross Coupling. A New Selective Method for C-C Bond Formation.W
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  220457. GABRIEL WEATHERHEAD
  220458. 16897
  220459. Negishi, E.B
  220460. Pure Appl. Chem.C
  220461. FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /ORGANOMETALLICS /TITANIUM /ZIRCONIUM  /NICKEL /PALLADIUM /C-M /Ti /Zr /Ni /Pd /CARBOMETALLATION /Al /COUPLING /C=C-C=C /E,Z  /C=C-C=C /E,E /C=C-M /Al /C=C-C-C-X /OH /C=C-X /Br /I /C=C-C-X /OHM
  220462. 17906N
  220463. 2/28/96V
  220464. Bimetallic Catalytic Systems Containing Titanium, Zirconium, Nickel, And Palladium. Their  Application to Selective Organic Synthesis.W
  220465. 1981X
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  220467. GABRIEL WEATHERHEAD
  220468. 16898
  220469. Negishi, E.//Brown, H. C.B    SynthesisC
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  220471. 17907N
  220472. 2/28/96
  220473. wVRThexylborane - A Highly Versatile Reagent for Organic Synthesis via Hydroboration.W
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  220475. GABRIEL WEATHERHEAD
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  220478. 17908N
  220479. 2/28/96V
  220480. Vinyl cations.W
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  220482. GABRIEL WEATHERHEAD
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  220485. J. Organomet. Chem.CpFUNCTIONAL GROUPS /TRANSFORMATIONS /ACETALS /C-X(Y) /O(O) /ORTHOESTERS /C-X(Y)(Z)  /O(O)(O) /HALOGENOSILANES /SiM
  220486. 17909N
  220487. 2/28/96VLReactions of acetals, orthoesters, and their analogues with halogenosilanes.W
  220488. 1988X
  220489. GABRIEL WEATHERHEAD
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  220491. Neale, R. S.B    SynthesisC[PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /ALKENES /C=C /RADICAL ADDITION  /C-X /NM
  220492. 17910N
  220493. 2/28/96VsNitrogen Radicals as Synthesis Intermediates. N-Haloamide Intermediates and Additions to  Unsaturated Hydrocarbons.W
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  220495. GABRIEL WEATHERHEAD
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  220498. 17911N
  220499. 2/28/96V3Thermal decomposition of aliphatic nitro compounds.W
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  220501. GABRIEL WEATHERHEAD
  220502. 16903
  220503. Natale, N. R.//Mirzaei, Y. R.B
  220504. Org. Prep. Proced. Int.M
  220505. 17912N
  220506. 2/28/96V%The lateral metalation of isoxazoles.W
  220507. 1993X
  220508. 515-56Y
  220509. GABRIEL WEATHERHEAD
  220510. 16904
  220511. Naso, F.B
  220512. Pure Appl. Chem.C
  220513. C-C BOND FORMATION /APPENDAGES /COUPLING /C=C-X /SPh,Br /C-M /Mg /X-C=C-Y /Br,S /COUPLING /C=C /DISUB /ALKENES /Ni /Pd /Fe /Cu /SM
  220514. 17913N
  220515. 2/28/96VPStereospecific Synthesis of Olefins through Sequential Cross-Coupling Reactions.W
  220516. 1988X
  220517. GABRIEL WEATHERHEAD
  220518. 16905
  220519. Newcomb, M.B
  220520. TetrahedronM
  220521. 17914N
  220522. 2/28/96VCCompetition methods and scales for alkyl-radical reaction kinetics.W
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  220524. 1151Y
  220525. GABRIEL WEATHERHEAD
  220526. 16906
  220527. Neumann, W. P.B
  220528. Chem. Rev.C'ORGANOMETALLICS /GERMANIUM /TIN /Ge /SnM
  220529. 17915N
  220530. 2/28/96V
  220531. Germylenes and stannylenes.W
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  220533. GABRIEL WEATHERHEAD
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  220535. AbNeumann, W. P.//Hillgaertner, H.//Baines, K. M.//Dicke, R.//Vorspohl, K.//Kobs, U.//Nussbeutel, U.B
  220536. TetrahedronC
  220537. 17916N
  220538. 2/28/96VNNew ways of generating organotin reactive intermediates for organic synthesis.W
  220539. 1989X
  220540. GABRIEL WEATHERHEAD
  220541. 16908
  220542. Neumann, W. P.B    SynthesisCFREAGENTS /Bu3SnH /TRIBUT LTIN HYDRIDE /HYDROMETALLATION /Sn /REDUCTIONM
  220543. 17917N
  220544. 2/28/96V8Tri-n-Butyl Tin Hydride as Reagent in Organic Synthesis.W
  220545. 1987X
  220546. GABRIEL WEATHERHEAD
  220547. 16909
  220548. Nesper, R.B
  220549. Angew. Chem., Int. Ed. Engl.M
  220550. 17918N
  220551. 2/28/96VEFullercages without carbon-fulleranes, fuller nes, space-filler-enes?W
  220552. 1994X
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  220554. GABRIEL WEATHERHEAD
  220555. 16910
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  220557. Acc. Chem. Res.C
  220558. 17919N
  220559. 2/28/96VsPatterns of Stoichiometric and Catalytic Reactions of Organozirconium and Related Complexes of  Synthetic Interest.W
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  220561. 124-30Y
  220562. GABRIEL WEATHERHEAD
  220563. 16911
  220564. Negishi, E.B
  220565. Pure Appl. Chem.M
  220566. 17920N
  220567. 2/28/96VNZipper-mode cascade carbometalation for construction of polycyclic structures.W
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  220569. GABRIEL WEATHERHEAD
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  220572. Chem. Scr.C
  220573. ORGANOMETALLICS /ZIRCONIUM /ZrM
  220574. 17921N
  220575. 2/28/96V\Cyclization, coupling, and rearrangement reactions of organozirconium and related c mpoumds.W
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  220577. GABRIEL WEATHERHEAD
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  220579. Negishi, E.//Takahashi, T.B    SynthesisC
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  220581. 17922N
  220582. 2/28/96V/Organozirconium Compounds in Organic Synthesis.W
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  220584. GABRIEL WEATHERHEAD
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  220586. Nicolaou, K. C.//Ogilvie, W. W.B
  220587. Chemtracts: Organic ChemistryC
  220588. TARGET SYNTHESIS /MACROLIDESM
  220589. 17923N
  220590. 2/28/96V<The total synthesis of Amphoteronolide B and Amphotericin B.W
  220591. 1990X
  220592. GABRIEL WEATHERHEAD
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  220595. TetrahedronC
  220596. TARGET SYNTHESIS /MACROLIDESM
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  220598. 2/28/96V
  220599. Synthesis of Macrolides.W
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  220601. GABRIEL WEATHERHEAD
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  220603. Nickon, A.B
  220604. Acc. Chem. Res.M
  220605. 17925N
  220606. 2/28/96VoNew perspectives on carbene rearrangements: migratory aptitudes, bystander assistance, and  geminal efficiency.W
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  220608. GABRIEL WEATHERHEAD
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  220610. Nicholas, K. M.B
  220611. Acc. Chem. Res.C>ORGANOMETALLICS /COBALT /ALKYNES /PROPARGYL CATION /C=C-C+ /CoM
  220612. 17926N
  220613. 2/28/96VFChemistry and Synthetic Utility of Cobalt-Complexed Propargyl Cations.W
  220614. 1987X
  220615. GABRIEL WEATHERHEAD
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  220618. 17927N
  220619. 2/28/96VGStrategies Employed in the Synthesis of Prostacyclins and Thromboxanes.W
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  220623. Newman, M. S.//Magerlein, B. J.B
  220624. Org. React. (N.Y.)M
  220625. 17928N
  220626. 2/28/96V(The Darzens Glycidic Ester Condensation.W
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  220628. GABRIEL WEATHERHEAD
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  220630. Newkome, G. R.B
  220631. Chem. Rev.M
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  220633. 2/28/96V
  220634. Pyridylphosphines.W
  220635. 1993X
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  220637. GABRIEL WEATHERHEAD
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  220640. Aldrichimica ActaM
  220641. 17930N
  220642. 2/28/96V-Building blocks for dendritic macromolecules.W
  220643. 1992X
  220644. GABRIEL WEATHERHEAD
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  220648. 17931N
  220649. 2/28/96V
  220650. Construction of Synthetic Macrocyclic Compounds Possessing Subheterocyclic Rings, Specifically  Pyridine, Furan, and Thiophene.W
  220651. 1977X
  220652. GABRIEL WEATHERHEAD
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  220654. Newkome, G. R., Ed.B
  220655. Tetrahedron Symposium-in-PrintCLC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /METALLATION /Ar-M /LiM
  220656. 17932N
  220657. 2/28/96V;Heteroatom-Directed Metallations in Heterocyclic Synthesis.W
  220658. 1 83X
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  220660. GABRIEL WEATHERHEAD
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  220662. A5Nishigaichi, Y.//Takuwa, A.//Naruta, Y.//Maruyama, K.B
  220663. TetrahedronC
  220664. 17933N
  220665. 2/28/96
  220666. VIVersatile roles of Lewis acids in the reactions of allylic tin compounds.W
  220667. 1993X
  220668. 7395-426Y
  220669. GABRIEL WEATHERHEAD
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  220671. Ninomiya, I.B
  220672. HeterocyclesCaC-C BOND FORMATION /ANNULATIONS /MISCELLANEOUS /PHOTOCHEMICAL REACTIONS  /PHOTOCHEMISTRY /ENAMIDEM
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  220674. 2/28/96WS1974  Application of Enamide Photocyclisation to the Synthesis of Natural Products.X
  220675. GABRIEL WEATHERHEAD
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  220680. 2/28/96V*Compounds containing phosphorus and boron.W
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  220682. GABRIEL WEATHERHEAD
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  220693. VfDerivatives of trivalent phosphorus in the synthesis of glycer phosphatides and related phospholipids.W
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  220698. Org. React. (N.Y.)CJC-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITION /ALDOL CONDENSATIONM
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  220700. 2/28/96V
  220701. The Aldol Condensation.W
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  220703. GABRIEL WEATHERHEAD
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  220706. Angew. Chem., Int. Ed. Engl.C
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  220708. 2/28/96VAIminophosphines: Unconventional compounds of main group elements.W
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  220710. GABRIEL WEATHERHEAD
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  220712. A'Nicolaou, K. C.//Dai, W.-M.//Guy, R. K.B
  220713. Angew. Chem., Int. Ed. Engl.M
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  220715. 2/28/96V
  220716. Chemistry and biology of taxol.W
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  220719. GABRIEL WEATHERHEAD
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  220722. Pure Appl. Chem.M
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  220724. 2/28/96VMProgress towards the total synthesis of the ene-diyne anticancer antibiotics.W
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  220727. GABRIEL WEATHERHEAD
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  220730. Angew. Chem., Int. Ed. Engl.M
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  220732. 2/28/96V#The battle of calicheamicin gamma1.W
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  220735. GABRIEL WEATHERHEAD
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  220738. Aldr chimica ActaM
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  220740. 2/28/96VMNew synthetic methods and strategies and total synthesis of natural products.W
  220741. 1993X
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  220743. GABRIEL WEATHERHEAD
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  220748. 2/28/96VIMolecular design, chemical synthesis, and biological action of enediynes.W
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  220750. GABRIEL WEATHERHEAD
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  220753. Pure Appl. Chem.C1FUNCTIONAL GROUPS /TRANSFORMATIONS /CARBOHYDRATESM
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  220755. 2/28/96V$Synthesis of novel oligosaccharides.W
  220756. 1991X
  220757. GABRIEL WEATHERHEAD
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  220760. Chemtracts: Organic ChemistryC
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  220763. 2/28/96V)Chemical synthesis of Glycosphingolipids.W
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  220765. GABRIEL WEATHERHEAD
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  220768. Angew. Chem., Int. Ed. Engl.M
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  220770. 2/28/96V9Chemistry and biology of enediyne anticancer antibiotics.W
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  220773. GABRIEL WEATHERHEAD
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  220778. 2/28/96V^Lipoxins and related eicosanoids: biosynthesis, biological properties, and chemical synthesis.W
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  220781. GABRIEL WEATHERHEAD
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  220783. A,Normant, J. F.//Marek, I.//Lefrancois, J. M.B
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  220787. 2/28/96V[Organobismetallic zinc reagents: their preparation and use in diastereoselective reactions.W
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  220792. Normant, J. F.B
  220793. New Journal of ChemistryC0ORGANOMETALLICS /GENERAL /C=C-M(M') /C-M(M') /BiM
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  220795. 2/28/96V=Organobismetallic reagents. Preparation and use in synthesis.W
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  220797. GABRIEL WEATHERHEAD
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  220802. 2/28/96V]Carbometallation (C-Metallation) of Alkynes: Stereospecific Synthesis of Alke yl Derivatives.W
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  220804. GABRIEL WEATHERHEAD
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  220808. 17952N
  220809. 2/28/96V(Organocopper (I) Compounds in Synthesis.W
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  220811. GABRIEL WEATHERHEAD
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  220814. Angew. Chem., Int. Ed. Engl.C#REAGENTS /SOLVENTS /CATALYSTS /HMPAM
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  220817. Hexamethylphosphoramide.W
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  220825. 2/28/96V8The chemistry of cyclopro ylmethyl and related radicals.W
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  220830. Nomura, T.B5Progress in the Chemistry of Organic Natural ProductsC
  220831. NATURAL PRODUCTSM
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  220833. 2/28/96V;Phenolic compounds of the mulberry tree and related plants.W
  220834. GABRIEL WEATHERHEAD
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  220837. Chem. Ind. (London)C
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  220839. 2/28/96V;The fascinating organometallic chemistry of phosphaalkynes.W
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  220842. GABRIEL WEATHERHEAD
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  220847. 2/28/96V5CH /  Interaction: Implic tions in Organic Chemistry.W
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  220853. SynlettM
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  220855. 2/28/96VSIntramolecular [2+2] Photocycloaddition Of Vinylarenes - Synthesis Of  Cyclophanes.W
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  220857. 884-894Z
  220858. GABRIEL WEATHERHEAD
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  220860. A    Nozoe, T.B
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  220863. 2/28/96VgCyclohepta[b][1,4]benzoxazine and its related compounds. Some novel aspects in heterocyclic  chemistry.W
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  220866. GABRIEL WEATHERHEAD
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  220868. Nozaki, H.B
  220869. SynlettC4PHYSICAL ORGANI  /REACTIVE INTERMEDIATES /CARBENOIDSM
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  220872. V3The Role of Metals in Carbene Synthon Introduction.W
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  220874. GABRIEL WEATHERHEAD
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  220877. TetrahedronM
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  220879. 2/28/96V8Organometallic ways for the multiplication of chirality.W
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  220882. GABRIEL WEATHERHEAD
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  220887. 2/28/96V/Asymmetric catalysis by chiral metal complexes.W
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  220893. Angew. Chem., Int. Ed. Engl.CrC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /1,2-ADDITION /ZINC /CHIRAL  AUXILIARY /CH RAL CATALYST /ZnM
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  220896. Enantioselective addition of organometallic reagents to carbonyl compounds: chirality transfer,  multiplication and amplification.W
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  220900. Noyori, R.//Suzuki, M.B
  220901. Chemtracts: Organic ChemistryC.TARGET SYNTHESIS /PROSTAGLANDINS /LEUKOTRIENESM
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  220904. VP n organometallic way to prostaglandins: The three-component coupling synthesis.W
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  220906. GABRIEL WEATHERHEAD
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  220909. Acc. Chem. Res.C2REAGENTS /CHIRAL AUXILIARY /CHIRAL CATALYST /BINAPM
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  220911. 2/28/96V<BINAP: an efficient chiral element for asymmetric catalysis.W
  220912. 1990X
  220913. GABRIEL WEATHERHEAD
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  220915. Noyori, R.B
  220916. Chem. Soc. Rev.C
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  220919. 2/28/96V?Chemical Multiplication of Chirality: Science and Applications.W
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  220921. GABRIEL WEATHERHEAD
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  220923. Noyori, R.//Hayakawa, Y.B
  220924. Org. React. (N.Y.)CiFUNCTIONAL GROUPS /MISCELLANEOUS /O=C-C-X /Cl /O=C-C-X /Br /HALOKETONES /METALS  /REDUCTION /O=C /KETONESM
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  220926. 2/28/96V`Reductive Dehalogenation of Polyhalo Ketones with Low-Valent Me als and Related Reducing Agents.W
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  220928. GABRIEL WEATHERHEAD
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  220931. Contemporary Organic Synthesis M
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  220937. GABRIEL WEATHERHEAD
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  220939. A    North, M.B
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  220941. 17969N
  220942. 2/28/96V+Catalytic asymmetric cyanohydrin synthesis.W
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  220945. GABRIEL WEATHERHEAD
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  220947. Normant, J.B
  220948. Chemtracts: Organic ChemistryC
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  220950. 17970N
  220951. 2/28/96VgSimple Organometallic Reagents for the Elaboration of More Sophisticated Ones and Multistep  Synthesis.W
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  220954. GABRIEL WEATHERHEAD
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  220956. A"Oediger, H.//Moller, F.//Eiter, K.B    SynthesisC)REAGENTS /DBU /DBN /AMIDINES /ELIMINATIONM
  220957. 17971N
  220958. 2/28/96V3Bicyclic Amidines as Reagents in Organic Synthesis.W
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  220960. GABRIEL WEATHERHEAD
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  220962. A&Oberhauser, T.//Faber, K.//Griengl, H.B
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  220965. 2/28/96VkA substrate model for the enzymic resolution of esters of bicyclic alcohols by Candida cylindracea  lipase.W
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  220968. GABRIEL WEATHERHEAD
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  220970. Oare, D. C.//Heathcock, C. H.B
  220971. Top. Stereochem.CRC-C BOND FORMATION /APPENDAGES /1,4-ADDITION /DIASTEREOGENIC REACTIONS /C=C-X /O,NM
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  220973. 2/28/96VPAcyclic stereocontrol in Michael addition reactions of enamines and enol ethers.W
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  220975. GABRIEL WEATHERHEAD
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  220978. Top. Stereochem.COC-C BOND FORMATION /APPENDAGES /1,4-ADDITION /PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  220980. 2/28/96V?Stereochemistry of the Base-Promoted Michael Addition Reaction.W
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  220982. GABRIEL WEATHERHEAD
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  220985. HeterocyclesM
  220986. 17975N
  220987. 2/28/96V-Small ring compounds containing sulfur atoms.W
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  220993. Adv. Heterocycl. Chem.C
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  220995. 2/28/96VkHeteroaromatic sulfoxides and sulfones: Ligand exchange and coupling in sulfuranes and  ipso-substitutions.W
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  220997. GABRIEL WEATHERHEAD
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  220999. Oae, S.//Furukawa, N.B
  221000. TetrahedronCeFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /SULFILIMINES  /ELIMINATION /SULFILIMINES /SM
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  221002. 2/28/96V3Ei Reaction of Sulphilimines and Related Compounds.W
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  221011. 2/28/96VkStructure, dynamics, and electronic properties of cobaltocene in tin sulfide selenide (SnS2-xSex)  {O<x<2}.W
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  221013. GABRIEL WEATHERHEAD
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  221015. O'Donnell, M. J., Ed.B
  221016. Tetrahedron Symposium-in-PrintCWFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /AMINO ACIDS /HOOC-C-X /NH  /AMINO ACIDSM
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  221018. 2/28/96V
  221019. alpha-Amino Acid Synthesis.W
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  221022. GABRIEL WEATHERHEAD
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  221027. 2/28/96V&Acidic and Basic Hydrolysis of Amides.W
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  221029. GABRIEL WEATHERHEAD
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  221031. A.O linkov, A. V.//Akhrem, I. S.//Vol'pin, M. E.B Russ. Chem. Rev. (Engl. Transl.)M
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  221033. 2/28/96VFThe structure of equimolar complexes of acid halides with Lewis acids.W
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  221035. GABRIEL WEATHERHEAD
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  221039. 2/28/96V8New aspects of stereoselective synthesis of 1,3-polyols.W
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  221041. GABRIEL WEATHERHEAD
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  221044. Acc. Chem. Res.C`FUNCTIONAL GROUPS /ENANTIOGENIC /O=C-R /KETONES /REDUCTION /STEREOSELECTIVE /C-X  /OH /ALCOHOLESM
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  221046. 2/28/96VaAn Introduction of Chiral Centres int  Acyclic Systems Based on Stereoselective Ketone Reduction.W
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  221048. GABRIEL WEATHERHEAD
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  221050. Ohno, M.//Otsuka, M.B
  221051. Org. React. (N.Y.)CPFUNCTIONAL GROUPS /BIOTRANSFORMATIONS /O=C-X /O  /PIG LIVER ESTERASE /HYDROLYSISM
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  221053. 2/28/96VDChiral synthons by ester hydrolysis catalyzed by pig liver esterase.W
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  221055. GABRIEL WEATHERHEAD
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  221058. Acc. Chem. Res.M
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  221060. 2/28/96VCStereoselective routes toward the synthesis of unusual amino acids.W
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  221062. GABRIEL WEATHERHEAD
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  221067. 2/28/96V6Reagent - controlled asymmetric Diels-Alder reactions.W
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  221072. Ogura, F.//Otsubo, T.//Aso, Y.B
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  221075. 2/28/96VBDesign and synthesis of novel chalcogen-containing organic metals.W
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  221083. 2/28/96VaArtificially elicited c pabilities of enzymes and their application in natural product chemistry.W
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  221085. GABRIEL WEATHERHEAD
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  221088. New Journal of ChemistryM
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  221090. 2/28/96VaThreading molecular strings onto molecular rings. Synthesis of rotaxanes by use of cyclodextrins.W
  221091. 1993X
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  221093. GABRIEL WEATHERHEAD
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  221098. 2/28/96VQHaworth Memorial Lecture - Exper ments Directed Towards Glycoconjugate  SynthesisW
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  221100. GABRIEL WEATHERHEAD
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  221102. A+Olah, G. A.//Iyer, P. S.//Prakash, G  K. S.B    SynthesisC
  221103. REAGENTS /NAFTION-HM
  221104. 17991N
  221105. 2/28/96VEPerfluorinated Resinsulphonic Acid (Nafion-H) Catalysis in Synthesis.W
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  221107. GABRIEL WEATHERHEAD
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  221109. Olah, G. A.//Narang, S. C.B
  221110. TetrahedronCDREAGENTS /Me3SiI /IODOTRIMETHYLSILANE /TRIMETHYLIODOSILANE /TMSI /SiM
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  221178. TetrahedronCQC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /CAMPHOR /CHIRAL AUX LIARYM
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  221519. SynlettM
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  221523. GABRIEL WEATHERHEAD
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  221525. Paquette, L. A.B
  221526. Angew. Chem., Int. Ed. Engl.CpC-C BOND F RMATION /PERICYCLIC REACTIONS /SIGMATROPIC /[3,3] /ANNULATION /MEDIUM RING /RING  CONTRACTION /N TO MM
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  221528. 2/28/96VRStereocontrolled construction of complex cyclic ketones by oxy-Cope rearrangement.W
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  221530. GABRIEL WEATHERHEAD
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  221535. 2/28/96V.Dodecahedranes and Allied Spherical Molecules.W
  221536. 1989X
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  221538. GABRIEL WEATHERHEAD
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  221540. Paquette, L. A.B
  221541. Chem. Rev.C+C-C BOND FORMATION /ANNULATIONS /3-RING /SiM
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  221543. 2/28/96V@Silyl-Substituted Cyclopropanes as Versatile Syn hetic Reagents.W
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  221545. GABRIEL WEATHERHEAD
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  221547. Paquette, L. A.B
  221548. Aldrichimica ActaC
  221549. TARGET SYNTHESIS /TERPENOIDS /UNNATURAL PRODUCTS /C-C BOND FORMATION  /ANNULATIONS /5-RING /CARBRING /5 /CYCLOPENTANES /NATURAL PRODUCTSM
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  221551. 2/28/96VHSynthetic Routes to Cyclopentanoid-Fused Unnatural and Natural Products.W
  221552. 1984X
  221553. GABRIEL WEATHERHEAD
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  221555. Paquette, L. A., Ed.B
  221556. Tetrahedron Symposium-in-PrintM
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  221558. 2/28/96V4Recent Developments in Polycyclopentanoid Chemistry.W
  221559. 1981Y
  221560. GABRIEL WEATHERHEAD
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  221562. Paquette, L. A.B
  221563. Org. React. (N.Y.)C
  221564. NAME REACTIONS /C-X(Y) /Br(SO2) /C-X(Y) /Cl(SO2) /SULFONES /EXTRUSION /CHELOTROPIC  REACTION /RAMBERG-BACKLUND REARRANGEMENT /ALKENES /C=C /SM
  221565. 18052N
  221566. 2/28/96V#The Ramberg-Backlund Rearrangement.W
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  221568. GABRIEL WEATHERHEAD
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  221571. Org. React. (N.Y.)M
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  221573. 2/28/96V
  221574. R duction with diimide.W
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  221576. GABRIEL WEATHERHEAD
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  221578. Pasto, D. J.B
  221579. TetrahedronC8FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /ALLENES /C=C=CM
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  221581. 2/28/96V(Recent Developments in Allene Chemistry.W
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  221584. GABRIEL WEATHERHEAD
  221585. 17046
  221586. Parsons, S.//Passmore, J.B
  221587. Acc. Chem.  es.M
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  221589. 2/28/96V=Rings, radicals, and synthetic metals: the Chemistry of SNS+.W
  221590. 1994X
  221591. 101-8Y
  221592. GABRIEL WEATHERHEAD
  221593. 17047
  221594. Parshall, G. W.//Nugent, W. A.B
  221595. CHEMTECHM
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  221597. 2/28/96V9Making pharmaceuticals via homogeneous catalysis. Part 1.W
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  221599. GABRIEL WEATHERHEAD
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  221601. A7Parshall, G. W.//Nugent, W. A.//Chan, D. M.-T.//Tam, W.B
  221602. Pure Appl. Chem.CkORGANOMETALLICS /GENERAL /ORGANIC SYNTHESIS /ALKYNES /ANNULATION /5-RING /C= -C-X /N /ARENES /W /Pd /Ti /CuM
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  221604. 2/28/96
  221605. VIA New Role for Organometallic Reactions in Organic Synthesis in Industry.W
  221606. 1985X
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  221608. GABRIEL WEATHERHEAD
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  221611. ORGANOMETALLICS /SILICON /SiM
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  221614. Reactions Proceedin  with Cleavage of Silicon-Carbon Bonds in Tetraorganosilanes and Formation of New Carbon-Carbon  Bonds under the Action of Lewis Acids: Applications to Organic Synthesis.W
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  221616. GABRIEL WEATHERHEAD
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  221618. Parmerter, S. M.B
  221619. Org. React. (N.Y.)M
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  221621. 2/28/96V<The Coupling of Diazonium Salts with Alipbatic Carbon Atoms.W
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  221623. GABRIEL WEATHERHEAD
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  221625. APParmar, V. S.//Prasad, A. K.//Sharma, N. K.//Bisht, K. S.//Sinha, R.//Taneja, P.B
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  221628. 2/28/96VhPotential applications of enzyme-mediated transesterifications in the synthesis of bioactive  compounds.W
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  221631. GABRIEL WEATHERHEAD
  221632. 17052
  221633. Parker, D.B
  221634. Chem. Rev.M
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  221636. 2/28/96
  221637. V)NMR determ nation of enantiomeric purity.W
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  221640. GABRIEL WEATHERHEAD
  221641. 17053
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  221643. Bull. Soc. Chim. Belg.C_C-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /PHOTOCHEMICAL REACTIONS  /PHOTOCHEMISTRYM
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  221645. 2/28/96V"Heteroaromatic Photosubstitutions.W
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  221647. GABRIEL WEATHERHEAD
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  221650. Acc. Chem. Res.CEC-C BOND FORMATION /AROMATICS /RING FUNCT ONALISATION /Ar-X /Ar-M /LiM
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  221654. GABRIEL WEATHERHEAD
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  221657. TetrahedronCGTARGET SYNTHESIS /MACROLIDES /MACROLIDES /NATURAL P ODUCTS /ANTIBIOTICSM
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  221659. 2/28/96V>Recent Developments in the Synthesis of Macrolide Antibiotics.W
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  221667. V`The  apor phase heterogeneous-catalytic hydrogenation of carbonyl compounds and carbon monoxide.W
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  221669. GABRIEL WEATHERHEAD
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  221671. A    Paust, J.B
  221672. Pure Appl. Chem.M
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  221674. 2/28/96V8Recent progress in commercial retinoids and carotenoids.W
  221675. 1991X
  221676. GABRIEL WEATHERHEAD
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  221678. Paulsen, H.B
  221679. Angew. Chem., Int. Ed. Engl.M
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  221681. 2/28/96VrSynthesis, conformations, and X-ray structure analysis of sacc aride chains from the core regions of glycoprotein.W
  221682. 1990X
  221683. GABRIEL WEATHERHEAD
  221684. 17059
  221685. Paulsen, H.B
  221686. Angew. Chem., Int. Ed. Engl.M
  221687. 18068N
  221688. 2/28/96VDAdvances in Selective Chemical Synthesis of Complex OligosaccharidesW
  221689. 1982X
  221690. GABRIEL WEATHERHEAD
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  221693. Chem. Ind. (Lond n)M
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  221695. 2/28/96V4Reaction systems for bulk pharmaceutical production.W
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  221697. GABRIEL WEATHERHEAD
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  221699. Patwardhan, S. A.B
  221700. Org. Prep. Proced. Int.M
  221701. 18070N
  221702. 2/28/96
  221703. V/Synthesis Of Alpha,Omega-Alkanediols - A ReviewW
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  221706. GABRIEL WEATHERHEAD
  221707. 17062
  221708. Patterson, J. M.B    SynthesisCDC-C BOND FORMATION /HETEROANNULATIONS /5-RING /PYRROLES,PYRROLENINESM
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  221712. GABRIEL WEATHERHEAD
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  221714. Pattenden, G.B
  221715. J. Heterocycl. Ch m.M
  221716. 18072N
  221717. 2/28/96V6Synthetic studies with natural oxazoles and thiazoles.W
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  221725. 2/28/96V7Cobalt-Mediated Radical Reactions in Organic Synthesis.W
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  221727. GABRIEL WEATHERHEAD
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  221729. Paton, R. M.B
  221730. C em. Soc. Rev.C
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  221734. V#The Chemistry of Nitrile Sulphides.W
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  221736. GABRIEL WEATHERHEAD
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  221739. Pure Appl. Chem.M
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  221741. 2/28/96VjNew methods and strategies for the stereocontrolled synthesis of polypropionate-derived natural  products.W
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  221756. 2/28/96V4Friedel-Crafts Acylation with Little or No Cata yst.W
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  221758. GABRIEL WEATHERHEAD
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  221764. GABRIEL WEATHERHEAD
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  221768. 2/28/96V1Preparation and Reactions of Di zomalonic Esters.W
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  221770. GABRIEL WEATHERHEAD
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  221775. 2/28/96V)Some chemistry of hindered organoboranes.W
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  221784. 2/28/96VVSynthesis and some properties of alkenyl carbanions stabilized by an alpha-boron atom.W
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  221786. GABRIEL WEATHERHEAD
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  221791. 2/28/96V6Carbon-Carbon Bond Formation Involving Boron Reagents.W
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  221793. GABRIEL WEATHERHEAD
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  221798. 2/28/96V:Synthesis of angular benzodipyrazoles and related systems.W
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  221800. GABRIEL WEATHERHEAD
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  221806. The Discovery o  Crown Ethers.W
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  221815. Multiple Stereocontrol Using Organometallic Complexes. Applications in Organic Synthesis and  Consideration of Futu e Prospects.W
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  221823. 2/28/96VBTricarbonyl(diene)iron Complexes: Synthetically Useful Properties.W
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  221831. +V"Potassium t-Butoxide in Synthesis.W
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  221838. 2/28/96V-Synthetic Applications of Tellurium Reagents.W
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  221840. GABRIEL WEATHERHEAD
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  221842. Petragnani, N.//Yonashiro, M.B    SynthesisCEC-C BOND FORMATION /APPENDAGES /ENOLATES /C=C-X-M /O-Li /ACIDS,ESTERSM
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  221844. 2/28/96VAThe Reactions of Dianions of Carboxylic Acids and Ester Enolates.W
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  221846. GABRIEL WEATHERHEAD
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  221848. .A"Petitou, M.//van Boeckel, C. A. A.B5Progress in the Chemistry of Organic Natural ProductsM
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  221850. 2/28/96V6Chemical synthesis of heparin fragments and analogues.W
  221851. 1992X
  221852. GABRIEL WEATHERHEAD
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  221854. Petersen, H.B    SynthesisCNFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /UREIDOALKYLATION /CYCLIC UREASM
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  221856. 2/28/96V4Syntheses of Cyclic Ureas by alpha-Ureidoalkylation.W
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  221858. GABRIEL WEATHERHEAD
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  221863. 2/28/96VHChemical modification of biopolymers with quinones and quinone methides.W
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  221865. GABRIEL WEATHERHEAD
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  221867. Petasis, N. A.//Patane, M. A.B
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  221870. 2/28/96V2The synthesis of carbocyclic eight-membered rings.W
  221871. 1992X
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  221873. GABRIEL WEATHERHEAD
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  221878. 2/28/96V0Organometallic intermediates: ultimat  reagents.W
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  221881. GABRIEL WEATHERHEAD
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  221886. 2/28/96VYCarbon-hydrogen bond activation by organometallics: the role of matrix isolation studies.W
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  221895. Chemistry of Spiroacetals.W
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  221903. 2/28/96V9Proton exchange in amides: Surprises from simple systems.W
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  221905. GABRIEL WEATHERHEAD
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  221907. Perlmutter, H. D.B
  221908. Adv. Heterocycl. Chem.M
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  221910. 2/28/96V=1,2-Diazocines, 1,3-diazocines, triazocines and tetrazocines.W
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  221912. GABRIEL WEATHERHEAD
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  221915. Adv. Heterocycl. Chem.M
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  221918. 1,4-Diazocines.W
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  221920. GABRIEL WEATHERHEAD
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  221926. 1,5-Diazocines.W
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  221933. 2/28/96V*Acyl nitroxides: reactions and reactivity.W
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  221935. GABRIEL WEATHERHEAD
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  221937. Pereira, S.//Srebnik, M.B
  221938. Aldrichimica ActaM
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  221940. 2/28/96V"The Ireland-Claisen rearrangement.W
  221941. 1993X
  221942. GABRIEL WEATHERHEAD
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  221944. Pfleiderer, W.//Gottlieb, R.B
  221945. HeterocyclesC]FUNCTIONAL GRO PS /TRANSFORMATIONS /ELECTROCHEMICAL REACTIONS /ELECTROCHEMISTRY /HETEROCYCLESM
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  221947. 2/28/96V2Electroorganic Syntheses of Nitrogen Heterocycles.W
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  221950. GABRIEL WEATHERHEAD
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  221952. Pfenniger, A.B    SynthesisC~C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /C=C-C-X /OH /SHARPLESS  EPOXIDATION /HETRING /3(O) /EPOXIDES /OXIRANESM
  221953. 18104N
  221954. 2/28/96VFAsymmetric Epoxidation of Allylic Alcohols: The Sharpless Epoxidation.W
  221955. 1986X
  221956. GABRIEL WEATHERHEAD
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  221958. Pfeffer, M.B
  221959. Pure Appl. Chem.C
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  221961. 2/28/96VkSelected applications to organic synthesis of intramolecular C-H activat on reactions by transition metals.W
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  221963. GABRIEL WEATHERHEAD
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  221965. Pfeffer, M.B
  221966. Recl. Trav. Chim. Pays-BasC
  221967. 18106N
  221968. 2/28/96VWReactions of cyclopalladated compounds and alkynes: new pathways for organic synthesis?W
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  221970. GABRIEL WEATHERHEAD
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  221972. Pfander, H.B
  221973. Pure Appl. Chem.M
  221974. 18107N
  221975. 2/28/96V4Synthesis of optically active carotenoids: a review.W
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  221977. GABRIEL WEATHERHEAD
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  221980. Nat. Prod. Rep.M
  221981. 18108N
  221982. 2/28/96V
  221983. Terpenoid glycosides.W
  221984. 1991X
  221985. GABRIEL WEATHERHEAD
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  221987. Pfaltz, A.B
  221988. Acc. Chem. Res.M
  221989. 18109N
  221990. 2/28/96VXChiral semicorrins and related nitrogen heterocycles as ligands in asymmetric catalysis.W
  221991. 1993X
  221992. 339-45Y
  221993. GABRIEL WEATHERHEAD
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  221995. Pez, G. P.//Armor, J. N.B
  221996. Adv. Organomet. Chem.C,ORGANOMET LLICS /TITANIUM /ZIRCONIUM /Ti /ZrM
  221997. 18110N
  221998. 2/28/96V(Chemistry of Titanocene and Zirconocene.W
  221999. 1981X
  222000. GABRIEL WEATHERHEAD
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  222002. Pettit, G. R.B5Progress in the Chemistry of Organic Natural ProductsM
  222003. 18111N
  222004. 2/28/96V
  222005. The bryostatins.W
  222006. 1991X
  222007. GABRIEL WEATHERHEAD
  222008. 17103
  222009. DA!Pettit, G. R.//van Tamelen, E. E.B
  222010. Org. React. (N.Y.)C
  222011. S /NiM
  222012. 18112N
  222013. 2/28/96
  222014. DV"Desulfurization with Raney Nickel.W
  222015. 1962X
  222016. GABRIEL WEATHERHEAD
  222017. 17104
  222018. Petrzilka, M.//Grayson, J. I.B    SynthesisCYC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /ANNULATIONS  /6-RING /DAM
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  222020. 2/28/96VGPreparation and Diels-Alder Reactions of Hetero-Substituted 1,3-Dienes.W
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  222022. GABRIEL WEATHERHEAD
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  222026. 2/28/96V#Sulfenamides and their derivatives.W
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  222032. 2/28/96VIElectrochemical methods for the generation of carbenes a d their analogs.W
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  222038. 2/28/96VITellurium reagents in organic synthesis: recent advances. Part 1, Part 2.W
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  222040. GABRIEL WEATHERHEAD
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  222043. 18117N
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  222046. GABRIEL WEATHERHEAD
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  222052. Coping With Extreme Lewis Acidity: Strategies for the Synthesis of Stable, Mononuclear  Organometallic Derivatives of Scandium.W
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  222054. GABRIEL WEATHERHEAD
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  222057. Pure Appl. Chem.CwC-C BOND FORMATION /ANNULATIONS /1,4-ADDITION /C=C-M /Sn /Cu /ANNULA ION /5-RING /6-RING /CARBRING /5 /CARBRING /6 /TINM
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  222059. 2/28/96V;The Use of Some Bifunctional Reagents in Organic Synthesis.W
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  222065. 2/28/96VFSynthesis Of 1,4-Dicarbonyl Compounds And Cyclopentenones From Furans.W
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  222072. 18121N
  222073. 2/28/96VDPyridinium Chlorochromate: A Versatile Oxidant i  Organic Synthesis.W
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  222075. GABRIEL WEATHERHEAD
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  222078. HeterocyclesC@C-C BOND FORMATION /ANNULATIONS /5-RING /FURANS /CYCLOPENTENONESM
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  222080. 2/28/96V1Advances in Cyclopentenone Synthesis from Furans.W
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  222090. GABRIEL WEATHERHEAD
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  222127. 2/28/96VyIndolo-2,3-quinodimethanes and stable cyclic analogs for regio- and stereocontrolled syntheses of  [b]-annelated indoles.W
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  222129. 1681Y
  222130. GABRIEL WEATHERHEAD
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  222136. 2/28/96VhNew Diels-Alder Reactions with Vinylindoles: A Regio-and Stereocontrolled Access to Annellated  Indoles.W
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  222139. GABRIEL WEATHERHEAD
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  222145. 2/28/96VjOrtho Esters and Dialkoxycarbenium Ions: Reactivity, Stability, Structure  and New Synthetic Applications.W
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  222147. GABRIEL WEATHERHEAD
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  222152. 2/28/96V8Pyrrole, pyrrolidine, piperidine, and azepine alkaloids.W
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  222154. GABRIEL WEATHERHEAD
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  222157. Nat. Prod. Rep.M
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  222159. 2/28/96
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  222166. 2/28/96V&The Hydrogenolysis of Organic Halides.W
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  222181. 2/28/96V)Organopseudohalosilanes II. Azidosilanes.W
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  222188. 2/28/96VwSingle and Double Nucleophilic Addition to Coordinated  -Hydrocarbons: Manganese-Mediated  Functionalization of Arenes.W
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  222195. 2/28/96VAPreparation Of Scalemic P-Chiral Phosphines And Their DerivativesW
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  222197. GABRIEL WEATHERHEAD
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  222203. 2/28/96VEMonocyclopentadienyl halide complexes of th  d- and f-block elements.W
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  222205. GABRIEL WEATHERHEAD
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  222207. Poirier, J. M.B
  222208. Org. Prep. Proced. Int.C_C-C BOND FORMATION /APPENDAGES /ENOLATES /ORGANOMETALLICS /ELEMENT /SILICON  /C=C-X-M /O-Si /SiM
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  222210. 2/28/96V<Synthesis and reactions of functionalized silyl enol ethers.W
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  222212. GABRIEL WEATHERHEAD
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  222215. Org. Prep. Proced. Int.C*C-C BOND FORMATION /APPENDAGES /ALKYLATIONM
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  222217. 2/28/96V5Regiospecific alkylation of cyclohexenones. A review.W
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  222219. GABRIEL WEATHERHEAD
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  222239. 2/28/96V$Recent Aspects of Carbene Chemistry.W
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  222246. 2/28/96VWThe Application of Thermolytic Reactions for the Synthesis of Fluoro-organic Compounds.W
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  222300. 2/28/96V>The Base-Promoted Rearrangements of Quaternary Ammonium Salts.W
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  222302. GABRIEL WEATHERHEAD
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  222307. 2/28/96V:The chemistry of thioph nium salts and thiophenium ylides.W
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  222316. GABRIEL WEATHERHEAD
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  222321. 2/28/96
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  222324. GABRIEL WEATHERHEAD
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  222329. 2/28/96VSPolyoxometalate chemistry. An old theme with new dimensions in several disciplines.W
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  222331. GABRIEL WEATHERHEAD
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  222337. 2/28/96VRReductions Promoted by Low Valent Transition Metal Complexes in Organic Synthesis.W
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  222344. 2/28/96V'Recent advances in 
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  222506. GABRIEL WEATHERHEAD
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  222792. 2/28/96V=Recent advance  in the synthesis of antibacterial quinolines.W
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  222830. 2/28/96V8Zinc borohydride - a reducing agent with high potential.W
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  222867. 2/28/96VTNon-bonding molecular orbitals and the chemistry of non-classical organic molecules.W
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  223022. 2/28/96V:Lewis Acid Induced alpha-alkylation of Carbonyl Compounds.W
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  223199. 2/28/96VQPhotoinduced charge separation via twisted intramolecular charge transfer states.W
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  223204. Angew. Chem., Int. Ed. Engl.C2F NCTIONAL GROUPS /BIOTRANSFORMATIONS /VITAMIN B12M
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  223206. 2/28/96VnEnzymic Reaction Selectivity by Negative Catalysis or How Do Enzymes Deal with Highly Reactive  Intermediates?W
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  223208. GABRIEL WEATHERHEAD
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  223210. Resnati, G.B
  223211. TetrahedronC
  223212. 18274N
  223213. 2/28/96V:Synthesis of chiral and bioactive fluoroorganic compounds.W
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  223216. GABRIEL WEATHERHEAD
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  223220. 2/28/96VEProgress in the field of physiologically active lanosterol compounds.W
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  223222. GABRIEL WEATHERHEAD
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  223227. 2/28/96VRSugars as chiral auxiliaries for the synthesis of enantiomerically pure compounds.W
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  223229. GABRIEL WEATHERHEAD
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  223232. Pure Appl. Chem.M
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  223234. 2/28/96V|The use of enzymes for the catalysis of key reactions in the synthesis of biologically active natural  products and analogs.W
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  223237. GABRIEL WEATHERHEAD
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  223246. GABRIEL WEATHERHEAD
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  223251. 2/28/96V=Cyclobutane Derivatives from Thermal Cycloaddition Reactions.W
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  223253. GABRIEL WEATHERHEAD
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  223256. 18280N
  223257. 2/28/96V6Synthetic transformations of vinyl and aryl triflates.W
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  223260. GABRIEL WEATHERHEAD
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  223264. 2/28/96V1Synthetic applications of the retro-ene reaction.W
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  223272. 2/28/96VTTransition metal promoted higher-order cycloadditio  reactions in organic synthesis.W
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  223280. 2/28/96
  223281. VE Methods for the Synthesis of Antiinflammatory 2-Arylpropionic Acids.W
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  223284. GABRIEL WEATHERHEAD
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  223289. 2/28/96VKPreparation of organometallic compounds from highly reactive metal powders.W
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  223298. 2/28/96VdPreparation of Highly Reactive Metal Powders and Their Use in Organic and Organometallic  Synthesis.W
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  223300. GABRIEL WEATHERHEAD
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  223305. 2/28/96V#The Conformation of Hydroxylamines.W
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  223312. 2/28/96V;The range of radical processes in nitration by nitric acid.W
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  223320. Diastereoselective cyclopropanations of chiral bicyclic lactams leading to enantiomerically pure  cyclopropanes. Application to the total synthesis of cis-(1S,3R)-deltamethrinic acid and dictyopterene  c'.W
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  223326. HeterocyclesCXC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /HETEROCYCLES  /BENZOPYRAN-4-ONEM
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  223336. 2/28/96VpGeometry and Conformational Properties of Some Five- and Six-Membered Heterocyclic  Compounds Containing O or S.W
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  223338. GABRIEL WEATHERHEAD
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  223341. Acc. Chem. Res.
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  223344. 2/28/96V4Synthesis of Leukotrienes and Lipoxygenase Products.W
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  223346. GABRIEL WEATHERHEAD
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  223351. 2/28/96VyChemistry Without Borders Betwee  Main Group and Transition Elements: Metal-Containing Cyclic Phosphazenes and Siloxanes.W
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  223358. 2/28/96V`Preparation of Aromatic Fluorine Compounds from Diazoniunn Fluoborates: The Schiemann  Reaction.W
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  223364. 2/28/96V$Cohalogenation in organic synthesis.W
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  223371. 2/28/96V}Progress in the chemistry of isobenzo urans: applications to the synthesis of natural products and polyaromatic hydrocarbons.W
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  223393. 2/28/96VOChemical and biological aspects of polyether-ionophore antibiotic biosynthesis.W
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  223395. GABRIEL WEATHERHEAD
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  223398. Nat. Prod. Rep.M
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  223407. Pure Appl. Chem.M
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  223409. 2/28/96VoExploitation of microbiological methods for the synthesis of biologically active natural products  and analogs.W
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  223412. GABRIEL WEATHERHEAD
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  223414. Rosini, G.//Balleni, R.B    SynthesisC
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  223417. 2/28/96VHFunctionalised Nitroalkenes as Useful Reagents for Alkyl Anion Synthons.W
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  223419. GABRIEL WEATHERHEAD
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  223421. A6Rosin , C.//Franzini, L.//Raffaelli, A.//Salvadori, P.B    SynthesisM
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  223423. 2/28/96VxSynthesis and applications of binaphthylic C2-symmetry derivatives as chiral auxiliaries in  enantioselective reactions.W
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  223430. 2/28/96VKRecent progress in the synthesis and reactivity of nitro ketones. A review.W
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  223438. 2/28/96VSThe chemistry of  icarbonylcyclopentadienyl iron complexes: Progress and prospects.W
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  223445. 2/28/96VJTransformation of Organoiron Complexes of Synthetic and Chemical Interest.W
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  223453. 2/28/96V@Organoiron Complexes as Potential Reagen s in Organic Synthesis.W
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  223477. 2/28/96V?Chirality and molecular recognition at the air-water interface.W
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  223484. 2/28/96VXArylation of Unsa urated Compounds by Diazonium Salts (The Meerwein Arylation Reaction).W
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  223568. 2/28/96VHSynthesis, Absolute Configuration, and Optical Purity of Chiral Allenes.W
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  223575. 2/28/96VRSynthesis of Medio-and Macrocyclic Compounds by High Dilution Priciple Techniques.W
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  223582. 2/28/96VDThe Consequences of Strain for the Structure of Aliphatic Molecules.W
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  223597. 2/28/96V%The Chemistry of Vicinal Polyketones.W
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  223604. 2/28/96VZElectrophilic bromination of carbon-carbon double bonds: structure, solvent and mechanism.W
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  223606. GABRIEL WEATHERHEAD
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  223608. Ruasse, M.-F.//Motallebi, S.B%Journal of Physical  rganic ChemistryM
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  223610. 2/28/96VySolvation, the electrophilic driving force of ionic bromination of ethylenic compounds. The  addition-solvolysis analogy.W
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  223612. GABRIEL WEATHERHEAD
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  223615. Acc. Chem. Res.M
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  223617. 2/28/96
  223618. VjBromonium ions or p-bromocarbocations in olefin bromination. A kinetic approach to product  selectivities.W
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  223620. GABRIEL WEATHERHEAD
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  223622. Rozwadowska, M. D.B
  223623. HeterocyclesM
  223624. 18329N
  223625. 2/28/96VLRecent Progress in the Enantioselective Synthesis of Isoquinoline Alkaloids.W
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  223632. 2/28/96V,Contemporary problems in methanol synthesis.W
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  223636. A    Rozen, S.B
  223637. Acc. Chem. Res.C8FUNCTIONAL GROUPS /PREPARATIONS /C-X /F /F2 /FLORINATIONM
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  223639. 2/28/96V]Elemental Fluorine as a 'Legitimate' Reagent for S lective Fluorination of Organic Compounds.W
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  223641. GABRIEL WEATHERHEAD
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  223643. Rozen, S.//Filler, R.B
  223644. TetrahedronCHFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /O=C-C-X /F /FLUORINATIONM
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  223651. Rozants v, E. G.//Sholle, V. D.B    SynthesisC2PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALSM
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  223653. 2/28/96VQSynthesis and Reactions of Stable Nitroxyl Radicals. I. Synthesis. II. Reactions.W
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  223655. GABRIEL WEATHERHEAD
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  223657. Roxburgh, C. J.B
  223658. TetrahedronM
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  223660. 2/28/96V<Syntheses of medium sized rings by ring expansion reactions.W
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  223665. Rowlinson, D. J.//Sosnovsky, G.B    SynthesisC|FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /C-H /ACYLOXYLATION /C-X /OAc  /ACETATES /O=C-C-X /OAc /ALPHA-ACETOXY KETONESM
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  223670. GABRIEL WEATHERHEAD
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  223675. 2/28/96V:The biochemical reactions of organometallics with enzymes.W
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  223677. GABRIEL WEATHERHEAD
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  223682. 2/28/96V_Mechanisms of intramolecular activation of carbon-hydrogen bonds in transition-metal complexes.W
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  223684. GABRIEL WEATHERHEAD
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  223689. 2/28/96V/Cyclopalladated Complexes in Organic Synthesis.W
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  223691. GABRIEL WEATHERHEAD
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  223693. Russell, G. A.B
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  223696. 2/28/96VDFree Radical Chain Reactions Involving Alkyl- and Alkenylmercurials.W
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  223698. GABRIEL WEATHERHEAD
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  223700. Russell, G. A.B
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  223703. 2/28/96VYFree Radical Chain Processes in Aliphatic Systems Involving an Electron Transfer Process.W
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  223705. GABRIEL WEATHERHEAD
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  223708. Adv. Organomet. Chem.
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  223711. 2/28/96V0Electron Transfer Reaction  n Organic Chemistry.W
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  223717. 2/28/96VbNew bis(naphthalic anhydrides) and polyheteroarylenes based on them with improved  processability.W
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  223719. GABRIEL WEATHERHEAD
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  223721. Ruffolo, R. R., Jr.B
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  223724. 2/28/96VCChirality in alpha- and beta-adrenoceptor agonists and antagonists.W
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  223737. 2/28/96VPIntramolecular Michael and anti-Michael additions to carbon-carbon triple bonds.W
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  223740. GABRIEL WEATHERHEAD
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  223742. Rudorf, W. D.B
  223743. Sulfur ReportsC
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  223745. 2/28/96V2Reactions of carbon disulfide with C-nucleophiles.W
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  223756. GABRIEL WEATHERHEAD
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  223761. 2/28/96VGSynthesis, reactions, and properties of oxygen-nitrogen-oxygen systems.W
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  223765. 1ALRuchardt, C.//Meier, M.//Haaf, K.//Pakusch, J.//Wolber, E. K. A.//Muller, B.B
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  223768. 2/28/96VMThe isocyani e-cyanide rearrangement: mechanism and preparative applications.W
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  223770. GABRIEL WEATHERHEAD
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  223772. Saini, N.//Sharma, P.B
  223773. HeterocyclesC
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  223775. 2/28/96Vq[Hydroxy(tosyloxy)iodo]benzene: a useful hypervalent iodine reagent for the synthesis of  heterocyclic compounds.W
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  223778. GABRIEL WEATHERHEAD
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  223781. Top. Curr. Chem.M
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  223783. 2/28/96V=Photoinduced electron transfer (PET) bond cleavage reactions.W
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  223785. GABRIEL WEATHERHEAD
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  223797. 2/28/96VWFrom atoms and bonds to three-dimensional atomic coordinates: automatic model builders.W
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  223825. 2/28/96VCMethods of replacing halogen in aromatic compounds by RS-functions.W
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  223830. Ryang, M.//Tsutsumi, S.B    SynthesisC+ORGANOMETALLICS /SYNTHESIS /METAL CARBONYLSM
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  223839. 2/28/96VOSpecial features of the synthesis of peptides containing secondary amino acids.W
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  223848. Optically Active Cyclopropanes.W
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  223866. GABRIEL WEATHERHEAD
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  223872. Metamorphosis of Synthetic Strategies with Allylic Silanes: Tetracoordina ed Allylic Silanes into Pentacoordinated Allylic Silicates.W
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  223877. Pure Appl. Chem.C
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  223880. 2/28/96VWSelective C-C Bond Formation Based on Organosilicon Reagents: Origins and Applications.W
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  223883. GABRIEL WEATHERHEAD
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  223885. AA$Sakata, G.//Makino, K.//Kurasawa, Y.B
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  223888. 2/28/96VKRecent Progress in Quinoxaline Chemistry. Synthesis and Biological Acivity.W
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  223894. Heterocycles
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  223897. 2/28/96VTSynthesis of Condensed Heteroaromatic Compounds Using Palladium-Catalysed Reactions.W
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  223900. GABRIEL WEATHERHEAD
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  223905. 2/28/96V;Application of chiral cyclic diols to asymmetric synthesis.W
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  223913. 2/28/96V=Recent Aspects of Singlet Oxygen Chemistry of Photooxidation.W
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  223916. GABRIEL WEATHERHEAD
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  223922. EV+Modern Methods of Aryl-Aryl Bond Formation.W
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  223925. GABRIEL WEATHERHEAD
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  223929. 2/28/96V,The Synthesis of 6H-Pyrido[4,3-b]carbazoles.W
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  223945. The lithium bond reexamined.W
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  223948. GABRIEL WEATHERHEAD
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  223952. C-C BOND FORMATION /HETEROANNULATIONS /4-RING /CARBENE /PEROXY ACID  /DICHLOROKETENE /IMINES /C=N-R /X=Y=Z /C,N,O /CYCLOADDITION /[2+2] /HETRING /4(N)M
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  223974. 2/28/96V The Chemistry of Pyrroloindoles.W
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  223981. 2/28/96V(1,10-Phenanthroline - A Versatile LigandW
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  223984. GABRIEL WEATHERHEAD
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  224002. Adv. Organomet. Chem.C
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  224019. 2/28/96V6Homogeneous Metal-Catalysis in Organic Photochemistry.W
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  224027. GABRIEL WEATHERHEAD
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  224032. 2/28/96VxSynthesis of enantiomerically pure secondary  amma-halo allylic alcohols and their use in the synthesis of leukotrienes.W
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  224052. 2/28/96V(Mechanisms of Hydrolysis of Thioacetals.W
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  224852. A*Sessler, J. L.//Cyr, M. J.//Burrell, A. K.B
  224853. SynlettM
  224854. 18492N
  224855. 2/28/96V5Sapphyrins: New Life for an Old 'Expanded Porphyrin'.W
  224856. 1991X
  224857. GABRIEL WEATHERHEAD
  224858. 17484
  224859. A    Servi, S.B    SynthesisM
  224860. 18493N
  224861. 2/28/96V/Bakers Yeast as a Reagent in Organic Synthesis.W
  224862. 1990X
  224863. GABRIEL WEATHERHEAD
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  224865. Serratosa, F.B
  224866. Acc. Chem. Res.CmFUNCTIONAL GROUPS / RANSFORMATIONS /DELTATE /SQUARATE /RHODIZONATE /CROCONATE /CARBRING /4  /CYCLOBUTENODIONEM
  224867. 18494N
  224868. 2/28/96V2Acetylene Diethers: A Logical Entry to Oxocarbons.W
  224869. 1983X
  224870. GABRIEL WEATHERHEAD
  224871. 17486
  224872. A-Serebryakov, E. P.//Hao, N. C.//Mavrov, M. V.B
  224873. Pure Appl. Chem.M
  224874. 18495N
  224875. 2/28/96V?Chiral building blocks based on technical grade 
  224876. -citronellene.W
  224877. 1990X
  224878. 2041Y
  224879. GABRIEL WEATHERHEAD
  224880. 17487
  224881. Seppelt, K.B
  224882. Angew. Chem., Int. Ed. Engl.C
  224883. F /SM
  224884. 18496N
  224885. 2/28/96V1Fluorine-stabilized sulfur-carbon multiple bonds.W
  224886. 1991X
  224887. GABRIEL WEATHERHEAD
  224888. 17488
  224889. Senning, A.B
  224890. Acc. Chem. Res.C2PHYSICAL ORGANIC /REACTIVE  NTERMEDIATES /RADICALSM
  224891. 18497N
  224892. 2/28/96V
  224893. How Free" are 'Free Radicals'?W
  224894. 1985X
  224895. GABRIEL WEATHERHEAD
  224896. 17489
  224897. Sen, A.B
  224898. Acc. Chem. Res.C:ORGANOMETALLICS /LANTHANIDES /ELECTROPHILIC TRANSITION /LaM
  224899. 18498N
  224900. 2/28/96V
  224901. Organometallic Chemistry of Electrophilic Transition and Lanthanide Metal Ions. The Dominant  Pathways for Reactions Involving C=C, C-C, and C-H Bonds.W
  224902. 1988X
  224903. GABRIEL WEATHERHEAD
  224904. 17490
  224905. AUSemmelhack, M. F.//Kim, C.//Zhang, N.//Bodurow, C.//Sanner, M.//Dobler, W.//Meier, M.B
  224906. Pure Appl. Chem.C
  224907. 18499N
  224908. 2/28/96VPIntramolecular alkoxycarbonylation of hydroxy alkenes promoted by palladium(II).W
  224909. 1990X
  224910. 2035Y
  224911. GABRIEL WEATHERHEAD
  224912. 17491
  224913. Semmelhack, M. F., Ed.B
  224914. Tetrahedron Symposium-in-PrintCCORGANOMETALLICS /SYNTHESIS /TARGET SYNTHESIS /C-M /NATURAL PRODUCTSM
  224915. 18500N
  224916. 2/28/96VXApplication of Newer Organometallic Reagents to the Total Synthesis of Natural Products.W
  224917. 1985X
  224918. 5741Y
  224919. GABRIEL WEATHERHEAD
  224920. 17492
  224921. Shea, K. J.B
  224922. TetrahedronClFUNCTIO AL GROUPS /PREPARATIONS /ALKENES /PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED  MOLECULES /C=CM
  224923. 18501N
  224924. 2/28/96VURecent Developments in the Synthesis, Structure, and Chemistry of Bridgehead Alkenes.W
  224925. 1980X
  224926. 1683Y
  224927. GABRIEL WEATHERHEAD
  224928. 17493
  224929. Shawali, A. S.B
  224930. Chem. Rev.M
  224931. 18502N
  224932. 2/28/96VKReactions of heterocyclic compounds with nitrilimines and their precursors.W
  224933. 1993X
  224934. 2731 77Y
  224935. GABRIEL WEATHERHEAD
  224936. 17494
  224937. Sharpless, K. B.B
  224938. TetrahedronM
  224939. 18503N
  224940. 2/28/96V
  224941. Coelacanths and catalysis.W
  224942. 1994X
  224943. 4235-58Y
  224944. GABRIEL WEATHERHEAD
  224945. 17495
  224946. A"Sharpless, K. B.//Verhoeven, T. R.B
  224947. Aldrichimica Acta
  224948. C-C BOND FORMATION /HETEROANNULATIONS /3-RING  REAGENTS /T-BUTYL HYDROPEROXIDE /t-BuOOH /OXIDATION /HETRING /3(O) /OXIRANES /EPOXIDESM
  224949. 18504N
  224950. 2/28/96V1Selective Oxygenation with t-Butyl Hydroperoxide.W
  224951. 1979X
  224952. GABRIEL WEATHERHEAD
  224953. 17496
  224954. Sharma, S.B
  224955. Sulfur ReportsC
  224956. C-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /FUNCTIONAL GROUPS  /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /X=Y=Z /N,C,S /SM
  224957. 18505N
  224958. 2/28/96V-Isothiocyanates in heterocyclic synthesis. 5.W
  224959. 1989X
  224960. GABRIEL WEATHERHEAD
  224961. 17497
  224962. A.Shapiro, E. A.//Dyatkin, A. B.//Nefedov, O. M.B Russ. Chem. Rev. (Engl. Transl.)M
  224963. 18506N
  224964. 2/28/96V
  224965. Carbene reactions of diazoesters with sigma-bonds as an effective method f r the alkoxycarbonylmethylenation of organic compounds.W
  224966. 1993X
  224967. GABRIEL WEATHERHEAD
  224968. 17498
  224969. Shapiro, Y. M.B Russ. Chem. Rev. (Engl. Transl.)M
  224970. 18507N
  224971. 2/28/96V'gem-Polyols-a unique class of compound.W
  224972. 1991X
  224973. 1036Y
  224974. GABRIEL WEATHERHEAD
  224975. 17499
  224976. Shapiro, R. H.B
  224977. Org. React. (N.Y.)CKFUNCTIONAL GROUPS /PREPARATIONS /C=N-X /NH-SO2 /SHAPIRO /C=C-M /Li /ALKENESM
  224978. 18508N
  224979. 2/28/96V
  224980. Alkenes from Tosylhydrazones.W
  224981. 1976X
  224982. GABRIEL WEATHERHEAD
  224983. 17500
  224984. A.Shambayati, S.//Crowe, W. E.//Schreiber, S. L.B
  224985. Angew. Chem., Int. Ed. Engl.CHPHYSICAL ORGANIC /STEREOCHEMISTRY /STEREOELECTRONICS /Li /Al /Ti /Sn /ZrM
  224986. 18509N
  224987. 2/28/96V{On the conformation and structure of organometal complexes in the solid state: two studies relevant  to chemical synthesis.W
  224988. 1990X
  224989. GABRIEL WEATHERHEAD
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  224991. A3Shafran, Y. Y. M.//Bakulev, V. A.//Mokrushin, V. S.B Russ. Chem. Rev. (Engl. Transl.)M
  224992. 18510N
  224993. 2/28/96V1Synthesis and properties of alpha-amino nitriles.W
  224994. 1989X
  224995. GABRIEL WEATHERHEAD
  224996. 17502
  224997. A2Shaban, M. A. E.//Taha, M. A. M.//Sharshira, E. M.B
  224998. Adv. Heterocycl. Chem.M
  224999. 18511N
  225000. 2/28/96VXSynthesis and biological activities of condensed heterocyclo[n,m-a,b, or c]quinazolines.W
  225001. 1991X
  225002. GABRIEL WEATHERHEAD
  225003. 17503
  225004. Shinkai, I.B
  225005. J. Heterocycl. Chem.M
  225006. 18512N
  225007. 2/28/96VZA practical asymmetric synthesis of a novel topically active carbonic anhydrase inhibitor.W
  225008. 1992X
  225009. 627-30Y
  225010. GABRIEL WEATHERHEAD
  225011. 17504
  225012. Shine, H. J.B%Journal of Physical Organic ChemistryM
  225013. 18513N
  225014. 2/28/96V@Reflections on the  -complex theory of benzidine rearrangements.W
  225015. 1989X
  225016. GABRIEL WEATHERHEAD
  225017. 17505
  225018. Shilov, A. E.B
  225019. New Journal of ChemistryC
  225020. 18514N
  225021. 2/28/96V_Dinitrogen fixation in solution in the presence of iron complexes. Intermediates and mechanism.W
  225022. 1992X
  225023. 213-18Y
  225024. GABRIEL WEATHERHEAD
  225025. 17506
  225026. Shilov, A. E.//Shul'pin, G. B.B Russ. Chem. Rev. (Engl. Transl.)M
  225027. 18515N
  225028. 2/28/96V:Activation of the carbon-hydrogen bond by metal complexes.W
  225029. 1990X
  225030. GABRIEL WEATHERHEAD
  225031. 17507
  225032. A#Shida, T.//Haselba k, E.//Bally, T.B
  225033. Acc. Chem. Res.C6PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICAL IONSM
  225034. 18516
  225035. 2/28/96V&Organic Radical Ions in Rigid Systems.W
  225036. 1984X
  225037. GABRIEL WEATHERHEAD
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  225039. Shibata, I.//Baba, A.B
  225040. Org. Prep. Proced. Int.C
  225041. 18517N
  225042. 2/28/96V(Organotin enolates in organic synthesis.W
  225043. 1994X
  225044. 85-100Y
  225045. GABRIEL WEATHERHEAD
  225046. 17509
  225047. Sheppard, R. C.B    Chem. Br.C
  225048. PEPTIDESM
  225049. 18518N
  225050. 2/28/96V%True automation of peptide synthesis.W
  225051. 1988X
  225052. GABRIEL WEATHERHEAD
  225053. 17510
  225054. Sheppard, W. A.B
  225055. Org. React. (N.Y.)CAFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /FLUORIDES /C-X /FM
  225056. 18519N
  225057. 2/28/96V8Modern Methods to Prepare Monofluoroaliphatic Compounds.W
  225058. 1974X
  225059. GABRIEL WEATHERHEAD
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  225061. A$Shen, .//Chen, W.//Jin, Y.//Shan, C.B
  225062. Pure Appl. Chem.C
  225063. 18520N
  225064. 2/28/96V8Syntheses and molecular structures of organolanthanoids.W
  225065. 1988X
  225066. 1251Y
  225067. GABRIEL WEATHERHEAD
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  225069. Sheldon, R. A.B
  225070. Top. Curr. Chem.M
  225071. 18521N
  225072. 2/28/96VJHomogeneous and heterogeneous catalytic oxidations with peroxide reagents.
  225073. 1993X
  225074. GABRIEL WEATHERHEAD
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  225076. Sheldon, R.B
  225077. Chem. Ind. (London)M
  225078. 18522N
  225079. 2/28/96V3Industrial synthesis of optically active compounds.W
  225080. 1990X
  225081. GABRIEL WEATHERHEAD
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  225083. Sheldon, R. A.//Kochi, J. K.B
  225084. Org. React. (N.Y.)C
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  225086. 18523N
  225087. 2/28/96VCOxidative Decarboxylation of Carboxylic Acids by Lead Tetraacetate.W
  225088. 1972X
  225089. GABRIEL WEATHERHEAD
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  225091. Sheehan, J. C.//Corey, E. J.B
  225092. Org. React. (N.Y.)M
  225093. 18524N
  225094. 2/28/96V
  225095. The Synthesis of 
  225096. -Lactams.W
  225097. 1957X
  225098. GABRIEL WEATHERHEAD
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  225100. Siedle, A. R.B
  225101. New Journal of ChemistryC
  225102. 18525N
  225103. 2/28/96V~Solid state chemistry of molecular metal oxide clusters. Carbon-hydrogen activation reactions of  an iridium polyoxometallate.W
  225104. 1989X
  225105. GABRIEL WEATHERHEAD
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  225107. Sicher, J.
  225108. Angew. Chem., Int. Ed. Engl.CHPHYSICAL ORGANIC /MECHANISMS /STEREOCHEMISTRY /ELIMINATION /ALKENES /C=CM
  225109. 18526N
  225110. 2/28/96VJThe Syn and Anti Steric Course in Bimolecular Olefin-Forming Eliminations.W
  225111. 1972X
  225112. GABRIEL WEATHERHEAD
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  225114. Sibi, M. P.B
  225115. Org. Prep. Proced. Int.M
  225116. 18527N
  225117. 2/28/96VAChemistry of N-methoxy-N-methylamides. Applications in synthesis.W
  225118. 1993X
  225119. GABRIEL WEATHERHEAD
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  225121. Shriner, R. L.B
  225122. Org. React. (N.Y.)C
  225123. 18528N
  225124. 2/28/96V
  225125. The Reformatsky Reaction.W
  225126. 1942X
  225127. GABRIEL WEATHERHEAD
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  225129. Shore, N. E.B
  225130. Org. React. (N.Y.)M
  225131. 18529N
  225132. 2/28/96VIThe Pauson-Khand cycloaddition reaction for synthesis of cyclopentenones.W
  225133. 1991X
  225134. GABRIEL WEATHERHEAD
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  225136. A    Shono, T.B
  225137. Top. Curr. Chem.M
  225138. 18530N
  225139. 2/28/96VRSynthesis of alkaloidal compounds using an electrochemical reaction as a key step.W
  225140. 1988X
  225141. GABRIEL WEATHERHEAD
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  225143. A#Shishkina, R. P.//Berezhnaya, V. N.
  225144. B Russ. Chem. Rev. (Engl. Transl.)M
  225145. 18531N
  225146. 2/28/96V5Photochemistry of 2-dialkylamino-1,4-naphthoquinones.W
  225147. 19 4X
  225148. GABRIEL WEATHERHEAD
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  225150. Shirley, D. A.B
  225151. Org. React. (N.Y.)C
  225152. Mg /Zn /CaM
  225153. 18532N
  225154. 2/28/96ViThe Synthesis of Ketones from Acid Halides and Organometallic Compounds of Magnesium, Zinc, and  Cadmium.W
  225155. 1954X
  225156. GABRIEL WEATHERHEAD
  225157. 17524
  225158. Shipchandler, M. T.B    SynthesisCGREAGENTS /HOOC-C-X /NO2 /ROOC-C-X /NO2 /NITROACETIC ACID /NITROACETATESM
  225159. 18533N
  225160. 2/28/96VDThe Utility of Nitroacetic Acid and Its Esters in Organic Synthesis.W
  225161. 1979X
  225162. GABRIEL WEATHERHEAD
  225163. 17525
  225164. Shiori, T.//Hamada, Y.B
  225165. HeterocyclesCYTARGET SYNTHESIS /MISCELLANEOUS /SYNTHON /OXAZOLES /HETEROCYCLES /OXAZOLES /AMINO  SUGARSM
  225166. 18534N
  225167. 2/28/96VhNatural Product Syntheses Utilizing 4-Alkoxycarbonyloxazoles as beta-hydroxy-alpha-amino acid  Synthons.W
  225168. 1988X
  225169. 1035Y
  225170. GABRIEL WEATHERHEAD
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  225172. Shinkai, S.B
  225173. TetrahedronM
  225174. 18535N
  225175. 2/28/96
  225176. V5Calixarenes - the third gene ation of supramolecules.W
  225177. 1993X
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  225179. GABRIEL WEATHERHEAD
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  225181. Simonet, J.//Le Guillanton, G.B
  225182. Bull. Soc. Chim. Fr.C\C-C BOND FORMATION /ANNULATIONS /MISCELLANEOUS /ELECTROCHEMICAL REACTIONS  /ELECTROCHEMISTRYM
  225183. 18536N
  225184. 2/28/96V+Cyclisations by Electrochemical Activation.W
  225185. 1986X
  225186. GABRIEL WEATHERHEAD
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  225188. A    Simon, Z.B
  225189. Angew. Chem., Int. Ed. Engl.C4PHYSICAL ORGANIC /STEREOELECTRONICS /STEREOCHEMISTRYM
  225190. 18537N
  225191. 2/28/96VVSpecific Interactions, Intermolecular Forces, Steric Requirements, and Molecular Size.W
  225192. 1974X
  225193. GABRIEL WEATHERHEAD
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  225195. A@Simmons, H. E.//Cairns, T. L.//Vladuchick, S. A.//Hoiness, C. M.B
  225196. Org. React. (N.Y.)CfC-C BOND FORMATION /ANNULATIONS /3-RING /CH2I2 /Zn-Cu /CYCLOPROPANATION  CYCLOPROPANE /CARBRING /3 /ZnM
  225197. 18538N
  225198. 2/28/96VSCyclopropanes from Unsaturated Compounds, Methylene Iodide, and Zinc-Copper Couple.W
  225199. 1973X
  225200. GABRIEL WEATHERHEAD
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  225203. Angew. Chem., Int. Ed. Engl.CbC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /BIOTRANSFORMATION  /REDUCTION /ENANTIOMERSM
  225204. 18539N
  225205. 2/28/96V8Chiral Compounds Synthesised by Biocatalytic Reductions.X
  225206. GABRIEL WEATHERHEAD
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  225208. A0Simkin, B. Y.//Minkin, V. I.//Glukhovtsev, M. N.B
  225209. Adv. Heterocycl. Chem.M
  225210. 18540N
  225211. 2/28/96V5The concept of aromaticity in heterocyclic chemistry.W
  225212. 1993X
  225213. GABRIEL WEATHERHEAD
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  225215. A5Simandi, L. I.//Barna, T.//Szeverenyi, Z.//Nemeth, S.B
  225216. Pure Appl. Chem.M
  225217. 18541N
  225218. 2/28/96V{Homogeneous catalytic oxidation of o-substituted anilines with dioxygen in the presence of cobalt  and manganese complexes.W
  225219. 1992X
  225220. 1511Y
  225221. GABRIEL WEATHERHEAD
  225222. 17533
  225223. Simamura, O.B
  225224. Top. Stereochem.CCPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /STEREOCHEMISTRYM
  225225. 18542N
  225226. 2/28/96V7The Stereochemistry of Cyclohexyl and Vinylic Radicals.W
  225227. 1970Y
  225228. GABRIEL WEATHERHEAD
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  225230. Silvester, M. J.B
  225231. Adv. Heterocycl. Chem.C
  225232. 18543N
  225233. 2/28/96V0Recent advances in fluoroheterocyclic chemistry.W
  225234. 1994X
  225235. GABRIEL WEATHERHEAD
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  225237. Silvester, M. J.B    Chem. Br.C
  225238. 18544N
  225239. 2/28/96V&Landmarks in organofluorine chemistry.W
  225240. 1993X
  225241. GABRIEL WEATHERHEAD
  225242. 17536
  225243. Silvester, M. J.B
  225244. Aldrichimica ActaC
  225245. 18545N
  225246. 2/28/96VOFl oroheterocyclic compounds: Synthesis, reactions and commercial applications.W
  225247. 1991X
  225248. GABRIEL WEATHERHEAD
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  225250. A.Sikora, D. J.//Macomber, D. W.//Raausch, M. D.B
  225251. Adv. Organomet. Chem.C9ORGANOMETALLICS /TITANIUM /ZIRCONIUM /HAFNIUM /Ti /Zr /HfM
  225252. 18546N
  225253. 2/28/96V9Carbonyl Derivatives of Titanium, Zirconium, and Hafnium.W
  225254. 1986X
  225255. GABRIEL WEATHERHEAD
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  225257. Siegel, H.B
  225258. Top. Curr. Chem.C_PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /CARBANIONS /C-M(X) /Li(Cl)  /CARBENES /LiM
  225259. 18547N
  225260. 2/28/96
  225261. VALithium Halocarbenoids. Carbenoids of High Synthetic Versatility.W
  225262. 1982X
  225263. GABRIEL WEATHERHEAD
  225264. 17539
  225265. A(Sliwa, W.//Chrzastek, L.//Mielniczak, M.B
  225266. HeterocyclesM
  225267. 18548N
  225268. 2/28/96V5Host-guest complexes of azaaromatic quaternary salts.W
  225269. 1993X
  225270. 1645-78Y
  225271. GABRIEL WEATHERHEAD
  225272. 17540
  225273. A)Sliwa, W.//Bachowska, B.//Zelichowicz, N.B
  225274. HeterocyclesM
  225275. 18549N
  225276. 2/28/96V
  225277. Chemistry of viologens.W
  225278. 1991X
  225279. 2241Y
  225280. GABRIEL WEATHERHEAD
  225281. 17541
  225282. Sliwa, W.//Mianowska, B.B
  225283. HeterocyclesCZFUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /PYRIDINIUM SALTS /CYCLISATIONS  REDUCTIONSM
  225284. 18550N
  225285. 2/28/96V
  225286. N-Substituted Pyridinium Salts.W
  225287. 1989X
  225288. GABRIEL WEATHERHEAD
  225289. 17542
  225290. A(Slivinskii, E. V.//Voitsekhovskii, Y. P.B Russ. Chem. Rev. (Engl. Transl.)M
  225291. 18551N
  225292. 2/28/96VODevelopment of ideas concerning the mechanism of the Fischer-Tropsch synthesis.W
  225293. 1989X
  225294. GABRIEL WEATHERHEAD
  225295. 17543
  225296. Skell, P. S.//Traynham, J. G.
  225297. Acc. Chem. Res.CPPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /C-X /Br /RADICAL BROMINATIONM
  225298. 18552N
  225299. 2/28/96VORadical Brominations of Alkyl Bromides and the Nature of 
  225300. -Bromoalkyl Radicals.W
  225301. 1984X
  225302. GABRIEL WEATHERHEAD
  225303. 17544
  225304. Skarzewski, J.//Siedlecka, R.B
  225305. Org. Pr p. Proced. Int.M
  225306. 18553N
  225307. 2/28/96V(Synthetic oxidations with hypochlorites.W
  225308. 1992X
  225309. GABRIEL WEATHERHEAD
  225310. 17545
  225311. A,Sizov, A. Y.//Kolomiets, A. F.//Fokin, A. V.B Russ. Chem. Rev. (Engl. Trans .)C
  225312. F /SM
  225313. 18554N
  225314. 2/28/96V"Polyfluoroalkylsulfenyl chlorides.W
  225315. 1992X
  225316. GABRIEL WEATHERHEAD
  225317. 17546
  225318. Sita, L. R.B
  225319. Acc. Chem. Res.C
  225320. 18555N
  225321. 2/28/96V1Heavy-Metal Organic Chemistry: Building with Tin.W
  225322. 1994X
  225323. 191-7Y
  225324. GABRIEL WEATHERHEAD
  225325. 17547
  225326. Siskin, M.//Katritzkcy, A. R.B
  225327. ScienceM
  225328. 18556N
  225329. 2/28/96VYReactivity of organic compounds in hot water: geochemical and technological implications.W
  225330. 1991X
  225331. GABRIEL WEATHERHEAD
  225332. 17548
  225333. A0Sinyashin, O. G.//Batyeva, E. S.//Pudovik, A. N.B Russ. Chem. R v. (Engl. Transl.)C
  225334. S /PM
  225335. 18557N
  225336. 2/28/96VLProgress in the chemistry of thio derivatives of trivalent phosphorous acid.W
  225337. 1989X
  225338. GABRIEL WEATHERHEAD
  225339. 17549
  225340. Sinnott, M. L.B
  225341. Adv. Phys. Org. Chem.C4PHYSICAL ORGANIC /STEREOELECTRONICS /STEREOCHEMISTRYM
  225342. 18558N
  225343. 2/28/96VOThe Principle of Least Nuclear Motion and the Theory of Stereoelectric Control.W
  225344. 1988X
  225345. GABRIEL WEATHERHEAD
  225346. 17550
  225347. Singh, V. K.B    SynthesisM
  225348. 18559N
  225349. 2/28/96VYPractica  and useful methods for the enantioselective reduction of unsymmetrical ketones.W
  225350. 1992X
  225351. GABRIEL WEATHERHEAD
  225352. 17551
  225353. A    Sinay, P.B
  225354. Pure Appl. Chem.C1FUNCTIONAL GROUPS /TRANSFORMATIONS /CARBOHYDRATESM
  225355. 18560N
  225356. 2/28/96V+Recent advances in glycosylation reactions.W
  225357. 1991X
  225358. GABRIEL WEATHERHEAD
  225359. 17552
  225360. Simpson, T. J.B
  225361. Nat. Prod. Rep.C'TARGET SYNTHESIS /MISCELLANEOUS /ARENESM
  225362. 18561N
  225363. 2/28/96
  225364. V3Benzenoid and Polycyclic Aromatic Natural Products.W
  225365. 1987X
  225366. GABRIEL WEATHERHEAD
  225367. 17553
  225368. Simpkins, N. S.B
  225369. TetrahedronCVFUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /C=C-X /SO2  /1,4-ADDITION /SM
  225370. 18562N
  225371. 2/28/96V The chemistry of vinyl sulfones.W
  225372. 1990X
  225373. 6951Y
  225374. GABRIEL WEATHERHEAD
  225375. 17554
  225376. AASimonova, T. P.//Nefedov, V. D.//Toropova, M. A.//Kirillov, N. F.B Russ. Chem. Rev. (Engl. Transl.)C
  225377. 18563N
  225378. 2/28/96V2Current approach to the problem of nitrenium ions.W
  225379. 1992X
  225380. GABRIEL WEATHERHEAD
  225381. 17555
  225382. Smith, M. B.B
  225383. Org. Prep. Proced. Int.C[C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2] /C=C-C=C-X /N  /CARBRING /6M
  225384. 18564N
  225385. 2/28/96VDN-Dienyl amides and lactams. Preparation and Diels-Alder reactivity.W
  225386. 1990X
  225387. GABRIEL WEATHERHEAD
  225388. 17556
  225389.     A    Smith, K.B
  225390. Bull. Soc. Chim. Fr.M
  225391. 18565N
  225392. 2/28/96V@Controlled organic synthesis with the aid of microporous solids.W
  225393. 1989X
  225394. GABRIEL WEATHERHEAD
  225395. 17557
  225396. Smith, J. G.B    SynthesisC
  225397. FUNCTIONAL GROUPS /TRANSFORMATIONS /EPOXIDE CLEAVAGE /HETRING /3(O) /EPOXIDES  /OXIRANES /DEOXYG NATION /ALLYLIC ALCOHOLS /C=C-C-X /OHM
  225398. 18566N
  225399. 2/28/96V+Synthetically Useful Reactions of Epoxides.W
  225400. 1984X
  225401. GABRIEL WEATHERHEAD
  225402. 17558
  225403. Smith, J. D.//Walton, D. R. M.B
  225404. Adv. Organomet. Chem.C
  225405. ORGANOMETALLICS /GENERAL /C-MM
  225406. 18567N
  225407. 2/28/96VSThe Organometallic Chemistry of the Main Group Elements. A Guide to the Literature.W
  225408. 1975X
  225409. GABRIEL WEATHERHEAD
  225410. 17559
  225411. Smith, P. A. S.//Baer, D. R.B
  225412. Org. React. (N.Y.)M
  225413. 18568N
  225414. 2/28/96V4The Demjanov and Tiffeneau-Demjanov Ring Exp nsions.W
  225415. 1960X
  225416. GABRIEL WEATHERHEAD
  225417. 17560
  225418. Smith, P. A. S.B
  225419. Org. React. (N.Y.)M
  225420. 18569N
  225421. 2/28/96V
  225422. The Curtius Reaction.W
  225423. 1946X
  225424. GABRIEL WEATHERHEAD
  225425. 17561
  225426. Smith, L. I.B
  225427. Org. React. (N.Y.)M
  225428. 18570N
  225429. 2/28/96V
  225430. The Jacobsen Reaction.W
  225431. 1942X
  225432. GABRIEL WEATHERHEAD
  225433. 17562
  225434. A)Smit, W. A.//Caple, R.//Smoliakova, I. P.B
  225435. Chem. Rev.M
  225436. 18571N
  225437. 2/28/96VWStepwise Electrophilic Addition - Some Novel Synthetic Ramifications Of  An Old ConceptW
  225438. 1994X    2359-2382Y
  225439. GABRIEL WEATHERHEAD
  225440. 17563
  225441. Smadja, W.B
  225442. SynlettM
  225443. 18572N
  225444. 2/28/96VfAcyclic diastereofacial selection in intermolecular radical reactions. Steric vs. electronic controls.W
  225445. 1994X
  225446. 1-26a
  225447. GABRIEL WEATHERHEAD
  225448. 17564
  225449. A    Sliwa, W.B
  225450. HeterocyclesM
  225451. 18573N
  225452. 2/28/96V9The reactivity of acridinium salts and related compounds.W
  225453. 1994X
  225454. 897-922Y
  225455. GABRIEL WEATHERHEAD
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  225457. A2Sobenina, L. N.//Mikhaleva, A. I.//Trofimov, B. A.B Russ. Chem. Rev. (Engl. Transl.)M
  225458. 18574N
  225459. 2/28/96V/Synthesis of pyrroles from aliphatic compounds.W
  225460. 1989X
  225461. GABRIEL WEATHERHEAD
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  225463. Soai, K.//Niwa, S.B
  225464. Chem. Rev.C
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  225466. 2/28/96V>Enantioselective addition of organozinc reagents to aldehydes.W
  225467. 1992X
  225468. GABRIEL WEATHERHEAD
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  225470. A1Soai, K.//Yokoyama, S.//Hayasaka, T.//Ebihara, K.B
  225471. C-C BOND FORMATION /APPENDAGES /1,4-ADDITION /ORGANOMETALLICS /ZINC /ENANTIOGENIC  REACTIONS STEREO HEMISTRY /ENONES /DIALKYLZINCS /C=C-C=O /C-M /Zn /ENANTIOSELECTIVE /O=C-RM
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  225473. 2/28/96V_Catalytic Asymmetric Induction in Enantioselective Conjugate Additions of Organozinc to Enones.W
  225474. 1988X
  225475. 4148Y
  225476. GABRIEL WEATHERHEAD
  225477. 17568
  225478. Snieckus, V.B
  225479. Pure Appl. Chem.M
  225480. 18577N
  225481. 2/28/96VtThe directed ortho metalation reaction. Methodology, applications, synthetic links, and a  nonaromatic ramification.W
  225482. 1990X
  225483. 2047Y
  225484. GABRIEL WEATHERHEAD
  225485. 17569
  225486. Snieckus, V.B
  225487. Pure Appl. Chem.C
  225488. 18578N
  225489. 2/28/96VVRegioselective synthetic processes based on the aromatic directed metalation strategy.W
  225490. 1990X
  225491. GABRIEL WEATHERHEAD
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  225493. Snieckus, V.B
  225494. Chem. Rev.CaORGANOMETALLICS /LITHIUM /C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGE  /METALLATION /Li /Ar-ArM
  225495. 18579N
  225496. 2/28/96
  225497. V{Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for  polysubstituted aromatica.W
  225498. 1990X
  225499. GABRIEL WEATHERHEAD
  225500. 17571
  225501. Snider, B.B
  225502. Chemtracts: Organic ChemistryM
  225503. 18580N
  225504. 2/28/96V"Carbofunctionalization of alkenes.W
  225505. 1991X
  225506. GABRIEL WEATHERHEAD
  225507. 17572
  225508. Snider, B. B.B
  225509. Acc. Chem. Res.C6C-C BOND FORMATION /PERICYCLIC REACTIONS / NE REACTIONM
  225510. 18581N
  225511. 2/28/96V#Lewis-Acid Catalyzed Ene Reactions.W
  225512. 1980X
  225513. GABRIEL WEATHERHEAD
  225514. 17573
  225515. Sneen, R. A.B
  225516. Acc. Chem. Res.CEPHYSICAL ORGANIC /MECHANISMS /SUBSTITUTION /NUCLEOPHILIC /ELIMINATIONM
  225517. 18582N
  225518. 2/28/96VZOrganic Ion Pairs as Intermediates in Nucleophilic Substitution and Elimination Reactions.W
  225519. 1973X
  225520. GABRIEL WEATHERHEAD
  225521. 17574
  225522. Sneden, A. T.B
  225523. SynlettM
  225524. 18583N
  225525. 2/28/96VESynthetic modifications of biologically interesting natural products.W
  225526. 1993X
  225527. 313-22a
  225528. GABRIEL WEATHERHEAD
  225529. 17575
  225530. Smith III, A. B.//Dieter, R. K.B
  225531. TetrahedronC4C-C BOND FORMATION /ANNULATIONS /5-RING /DIAZOKETONEM
  225532. 18584N
  225533. 2/28/96V6The Acid Promoted Decomposition of alpha-Diazoketones.W
  225534. 1981X
  225535. 2407Y
  225536. GABRIEL WEATHERHEAD
  225537. 17576
  225538. Sonoda, N.B
  225539. Pure Appl. Chem.C
  225540. 18585N
  225541. 2/28/96V5Selenium-assisted carbonylation with carbon monoxide.W
  225542. 1993X
  225543. 699-706Y
  225544. GABRIEL WEATHERHEAD
  225545. 17577
  225546. Sonnet, P. E.B
  225547. TetrahedronCLFUNCTIONAL GROUPS /PREPARATIONS /ALKENES /C=C /INVERSION /ISOMERIZATION /C=CM
  225548. 18586N
  225549. 2/28/96V
  225550. Olefin Inversion.W
  225551. 1980X
  225552. GABRIEL WEATHERHEAD
  225553. 17578
  225554. A=Sonawane, H. R.//Bellur, N. S.//Ahuja, J. R.//Kulkarni, D. G.B
  225555. Tetrahedron: AsymmetryM
  225556. 18587N
  225557. 2/28/96V
  225558. Recent developments in the synthesis of optically active alpha-arylprop noic acids: an important class of non-steroidal anti-inflammatory agents.W
  225559. 1992X
  225560. GABRIEL WEATHERHEAD
  225561. 17579
  225562. Somsak, L.//Ferrier, R. J.B
  225563. Adv. Carbohydr. Chem. Biochem.M
  225564. 18588N
  225565. 2/28/96
  225566.  V@Radical-Mediated Brominations At Ring Positions Of CarbohydratesW
  225567. 1991X
  225568. 37-92Y
  225569. GABRIEL WEATHERHEAD
  225570. 17580
  225571. Sommer, J.//Bukala, J.B
  225572. Acc. Chem. Res.M
  225573. 18589N
  225574. 2/28/96V.Selective electrophilic activation of alkanes.W
  225575. 1993X
  225576. 370-76Y
  225577. GABRIEL WEATHERHEAD
  225578. 17581
  225579. Sommer, L. H.B
  225580. Angew. Chem., Int. Ed. Engl.C.PHYSICAL ORGANIC /STEREOCHEMIS RY /SILICON /SiM
  225581. 18590N
  225582. 2/28/96V/The Stereochemistry of Organosilicon Compounds.W
  225583. 1962X
  225584. GABRIEL WEATHERHEAD
  225585. 17582
  225586. Solladie, G.B
  225587. Pure Appl. Chem.C
  225588. ASYMMETRIC SYNTHESISM
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  225590. 2/28/96VLRecent results in the field of asymmetric synthesis using chiral sulfoxides.W
  225591. 1988X
  225592. 1699Y
  225593. GABRIEL WEATHERHEAD
  225594. 17583
  225595. Solladie, GM
  225596. 18592N
  225597. 2/28/96a
  225598. GABRIEL WEATHERHEAD
  225599. 17584
  225600. %A    Solff, H.B
  225601. Org. React. (N.Y.)M
  225602. 18593N
  225603. 2/28/96V
  225604. The Schmidt Reaction.W
  225605. 1946X
  225606. GABRIEL WEATHERHEAD
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  225608. &A0Sokolyuk, N. T.//Romanov, V. V.//Pisulina, L. P.
  225609. &B Russ. Chem. Rev. (Engl. Transl.)M
  225610. 18594N
  225611. 2/28/96V.Naphthacenequinones: synthesis and properties.W
  225612. 1993X
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  225614. GABRIEL WEATHERHEAD
  225615. 17586
  225616. 'A1Sokolovskii, V. D.//Yur'eva, T. M.//Matros, Y. S.M
  225617. 18595N
  225618. 2/28/96a
  225619. GABRIEL WEATHERHEAD
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  225621. (A!Sokolov, V. I.//Stankevich, I. V.B Russ. Chem. Rev. (Engl. Transl.)M
  225622. 18596N
  225623. 2/28/96VnThe fullerenes - new allotropic forms of carbon: molecular and electronic structure, and chemical  properties.W
  225624. 1993X
  225625. GABRIEL WEATHERHEAD
  225626. 17588
  225627. Soderquist, J. A.B
  225628. Aldrichimica ActaC
  225629. 18597N
  225630. 2/28/96V)Samarium(II) iodide in organie synthesis.W
  225631. 1991X
  225632. GABRIEL WEATHERHEAD
  225633. 17589
  225634. Sodeoka, M.//Shibasaki, M.B    SynthesisC
  225635. 18598N
  225636. 2/28/96VDArene chromium tricarbonyl cataly ed reactions in organic synthesis.W
  225637. 1993X
  225638. 643-58a
  225639. GABRIEL WEATHERHEAD
  225640. 17590
  225641. Stang, P. J.B
  225642. Chem. Rev.C>PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /CARBENESM
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  225644. 2/28/96
  225645. Unsaturated Carbenes.W
  225646. 1978X
  225647. GABRIEL WEATHERHEAD
  225648. 17591
  225649. Stang, P. J.B
  225650. Acc. Chem. Res.C~PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS /CARBENOIDS  /C=C-X /OTf /VINYL TRIFLATES /C+ /CARBENESM
  225651. 18600N
  225652. 2/28/96V;Vinyl Triflate Chemistry: Unsaturated Cations and Carbenes.W
  225653. 1978X
  225654. GABRIEL WEATHERHEAD
  225655. 17592
  225656. Stanek, J.B
  225657. Top. Curr. Chem.M
  225658. 18601N
  225659. 2/28/96VLPreparation of selectively alkylated saccharides as synthetic intermediates.W
  225660. 1990a
  225661. GABRIEL WEATHERHEAD
  225662. 17593
  225663. Stammer, C. H.B
  225664. TetrahedronM
  225665. 18602N
  225666. 2/28/96V8Cyclopropano Amino Acids (2,3- and 3,4-Methamino Acids).W
  225667. 1990X
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  225669. GABRIEL WEATHERHEAD
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  225671. /A#Stadnichuk, M. D.//Voropaeva, T. I.B Russ. Chem. Rev. (Engl. Trans .)C
  225672. 18603N
  225673. 2/28/96V@Silicon-containing 1,3-alkenynes and more unsaturated compounds.W
  225674. 1992X
  225675. 1091Y
  225676. GABRIEL WEATHERHEAD
  225677. 17595
  225678. Stadlbauer, W.//Kappe, T.B
  225679. HeterocyclesM
  225680. 18604N
  225681. 2/28/96
  225682. 0V@Simple and effective approaches to coumestans and azacoumestans.W
  225683. 1993X
  225684. 1425-40Y
  225685. GABRIEL WEATHERHEAD
  225686. 17596
  225687. Stach, H.//Hesse, M.B
  225688. TetrahedronC/C-C BOND FORMATION /ANNULATIONS /RING EXPANSIONM
  225689. 18605N
  225690. 2/28/96V7Synthesis of Macrocyclic Compounds by Ring Enlargement.W
  225691. 1988X
  225692. 1573Y
  225693. GABRIEL WEATHERHEAD
  225694. 17597
  225695. Stacey, F. W.//Harris, J. F.B
  225696. Org. React. (N.Y.)C[PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /ALKENES /C=C /AKLYNES /CC /RADICAL  ADDITION /C-XM
  225697. 18606N
  225698. 2/28/96VfFormation of Carbon-Heteroatom Bonds by Free Radical Chain Additions to Carbon-Carbon Multiple  Bonds.W
  225699. 1963X
  225700. GABRIEL WEATHERHEAD
  225701. 17598
  225702. St. Clair Black, D.//Kumar, N.B
  225703. Org. Prep. Proced. Int.M
  225704. 18607N
  225705. 2/28/96V
  225706. Pyrroloquinolines.W
  225707. 1991X
  225708. GABRIEL WEATHERHEAD
  225709. 17599
  225710. Squires, R. R.B
  225711. Acc. Chem. Res.M
  225712. 18608N
  225713. 2/28/96V
  225714. Gas-phase carbanion chemistry.W
  225715. 1992X
  225716. GABRIEL WEATHERHEAD
  225717. 17600
  225718. Spoerri, P. E.//DuBois, A. S.B
  225719. Org. React. (N.Y.)M
  225720. 18609N
  225721. 2/28/96V
  225722. The Hoesch Synthesis.W
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  226177. 2/28/96V#Cyclophanes as synthetic receptors.W
  226178. 1990X
  226179. GABRIEL WEATHERHEAD
  226180. 17661
  226181. Sutherland, J. K.
  226182. Chem. Soc. Rev.C6C-C BOND FORMATION /ANNULATIONS /MISCELLANEOUS /6-RINGM
  226183. 18670N
  226184. 2/28/96VIThe Initiation of Cyclisation Using 3-Methylcyclohe -2-enone Derivatives.W
  226185. 1980X
  226186. GABRIEL WEATHERHEAD
  226187. 17662
  226188. Suter, C. M.//Weston, A. W.B
  226189. Org. React. (N.Y.)C
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  226191. 2/28/96VJDirect Sulfonation of Aromatic Hydrocarbons and Their Halogen Derivatives.W
  226192. 1946X
  226193. GABRIEL WEATHERHEAD
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  226195. Takahata, H.//Yamazaki, T.B
  226196. HeterocyclesCzC-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESIS /C=C-X-M /N-Li /C=C-X(Y)  /N(S) /S=C-N /THIOAMIDE /HETEROCYCLES /SM
  226197. 18672N
  226198. 2/28/96V1Synthesis of Heterocycles using Thioamide Groups.W
  226199. 1988X
  226200. 1953Y
  226201. GABRIEL WEATHERHEAD
  226202. 17664
  226203. Takahashi, M.//Okazaki, R.B
  226204. Sulfur ReportsC
  226205. 18673N
  226206. 2/28/96V'The chemistry of thionitroso compounds.W
  226207. 1993X
  226208. 293-341Y
  226209. GABRIEL WEATHERHEAD
  226210. 17665
  226211. Takahashi, K.B
  226212. Pure Appl. Chem.M
  226213. 18674N
  226214. 2/28/96
  226215. vV]Conjugation-extended ring assemblies with central heterocycles. New multistage redox system .W
  226216. 1993X
  226217. GABRIEL WEATHERHEAD
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  226219. Tadayoni, B. M.//Rebek, J., Jr.B%Journal of Physical Organic ChemistryM
  226220. 18675N
  226221. 2/28/96V,Stereoelectronic effects at carboxyl oxygen.W
  226222. 1992X
  226223. 683-8Y
  226224. GABRIEL WEATHERHEAD
  226225. 17667
  226226. Taber, D. F.B
  226227. C-C BOND FORMATION /ANNULATIONS /MISCELLANEOUS /ENOLATES /ANNULATION  /ENANTIOSELECTIVE /CHIRAL AUXILIARY /ALKYLATION /SPIROCYCLESM
  226228. 18676N
  226229. 2/28/96V#Enantioselective Ring Construction.W
  226230. 1987X
  226231. GABRIEL WEATHERHEAD
  226232. 17668
  226233. Ta-shma, R.//Rappoport, Z.B
  226234. Adv. Phys. Org. Chem.M
  226235. 18677N
  226236. 2/28/96VbSolvent-induced changes in the selectivity of solvolyses in aqueous alcohols and relatet mixtures.W
  226237. 1992X
  226238. GABRIEL WEATHERHEAD
  226239. 17669
  226240. T., Wagner-JaureggB    SynthesisC<C-C BOND FORMATION /HETEROANNULATIONS /6-RING /AZINES,IMINESM
  226241. 18678N
  226242. 2/28/96
  226243. zVOReactions of Azines and Imines (Azomethines and Schiff Bases) with Dienophiles.W
  226244. 1976X
  226245. GABRIEL WEATHERHEAD
  226246. 17670
  226247. Szabo, W. A.B
  226248. Aldrichimica ActaC
  226249. 18679N
  226250. 2/28/96VIChlorosulfonyl Isocyanate. Silver Anniversary of a Lively Heterocumulene.W
  226251. 1977X
  226252. GABRIEL WEATHERHEAD
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  226254. Swindell, C. S.B
  226255. Org. Prep. Proced. Int.M
  226256. 18680N
  226257. 2/28/96V&Taxane diterpene synthesis strategies.W
  226258. 1991X
  226259. GABRIEL WEATHERHEAD
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  226261. }A    Swern, D.B
  226262. Org. React. (N.Y.)M
  226263. 18681N
  226264. 2/28/96VKEpoxidation and Hydroxylation of Ethylenic Compounds with Organic Peracids.W
  226265. 1953X
  226266. GABRIEL WEATHERHEAD
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  226268. Taylor, R. J. K.B    SynthesisCSORGANOMETALLICS /COPPER /C-C BOND FORMATION /APPEN AGES /1,4-ADDITION /ENOLATES /CuM
  226269. 18682N
  226270. 2/28/96V;Organocopper Conjugate Addition-Enolate Trapping Reactions.W
  226271. 1985X
  226272. GABRIEL WEATHERHEAD
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  226274. Taylor, K. G.B
  226275. Tetrahedron
  226276. C>PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBENOIDS /CARBENESM
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  226278. 2/28/96V5Carbenes and Carbenoids with Neighboring Heteroatoms.W
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  226281. GABRIEL WEATHERHEAD
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  226283. Taylor, E. C.//Turchi, I. J.B
  226284. Che . Rev.CdC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[M+N] /1,5-DIPOLAR  /CYCLOADDITIONS /[5+2]M
  226285. 18684N
  226286. 2/28/96V
  226287. 1,5-Dipolar Cyclisations.W
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  226289. GABRIEL WEATHERHEAD
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  226291. Taylor, E. C.//McKillop, A.B
  226292. Acc. Chem. Res.C
  226293. ORGANOMETALLICS /THALLIUM /TlM
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  226295. 2/28/96V
  226296. Thallium in Organic Synthesis.W
  226297. 1970X
  226298. GABRIEL WEATHERHEAD
  226299. 17677
  226300. Tashiro, M.B    SynthesisCIC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /ARENE  /PROTECTIONM
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  226302. 2/28/96VMSelective Synthesis of Aromatic Compounds Using Positional Protective Groups.W
  226303. 1979X
  226304. GABRIEL WEATHERHEAD
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  226306. Tarbell, D. S.B
  226307. Org. React. (N.Y.)M
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  226309. 2/28/96V
  226310. The Claisen Rearrangement.W
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  226312. GABRIEL WEATHERHEAD
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  226321. Angew. Chem , Int. Ed. Engl.M
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  226323. 2/28/96VNChiral aziridines. Their synthesis and use in stereoselective transformations.W
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  226326. GABRIEL WEATHERHEAD
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  226328. Tanner, D.B
  226329. Pure Appl. Chem.M
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  226331. 2/28/96V1Stereocontrolled synthesis via chiral aziridines.W
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  226334. GABRIEL WEATHERHEAD
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  226336. A!Tamura, R.//Kamimura, A.//Ono, N.B    SynthesisC*C-C BOND FORMATION /APPENDAGES /ALKYLATIONM
  226337. 18691N
  226338. 2/28/96VMDisplacement of aliphatic nitro groups by carbon and heteroatom nucleophiles.W
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  226340. GABRIEL WEATHERHEAD
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  226342. A%Tamura, Y.//Minamikawa, J.//Ikeda, M.B    SynthesisC6REAGENTS /O-MESITYLENESULFONYLHYDROXYLAMINE /AMINATIONM
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  226344. 2/28/96
  226345. VSO-Mesitylenesul onylhydroxylamine and Related Compounds. Powerful Aminating Agents.W
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  226347. GABRIEL WEATHERHEAD
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  226349. Tamm, C.B
  226350. Pure Appl. Chem.M
  226351. 18693N
  226352. 2/28/96VUPig liver esterase catalyzed hydrolysis: substrate specificity and stereoselectivity.W
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  226355. GABRIEL WEATHERHEAD
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  226357. Tamm, C.//Jeker, N.B
  226358. TetrahedronM
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  226360. 2/28/96V2Synthesis of macrocyclic trichothecene mycotoxins.W
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  226362. 2385Y
  226363. GABRIEL WEATHERHEAD
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  226365. A!Tamao, K.//Kobayashi, K.//Ito, Y.B
  226366. SynlettC
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  226368. 2/28/96V[Ni kel(0)-mediated intramolecular cyclizations of enynes, dienynes, bis-dienes, and diynes.W
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  226370. GABRIEL WEATHERHEAD
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  226372. A$Thebtaranonth, C.//Thebtaranonth, Y.B
  226373. TetrahedronC
  226374. CYCLISATION /Pd /Ni /Hg /Cr /SmM
  226375. 18696N
  226376. 2/28/96V&Developments in Cyclisation Reactions.W
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  226379. GABRIEL WEATHERHEAD
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  226384. 2/28/96
  226385. VIMechanism and catalysis of nucleophilic substitution in phosphate esters.W
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  226387. GABRIEL WEATHERHEAD
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  226390. Sulfur ReportsC
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  226392. 2/28/96V]Naturally occurring 1,2-dithiolanes and 1,2,3-trithianes. Chemical and biological properties.W
  226393. 1990X
  226394. GABRIEL WEATHERHEAD
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  226396. Terashima, M.//Ishikura, M.B
  226397. Adv. Heterocycl. Chem.C
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  226399. 2/28/96V+Boron-substituted heteroaromatic compounds.W
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  226401. GABRIEL WEATHERHEAD
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  226403. Terao, Y.//Aono, MM
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  226405. 2/28/96a
  226406. GABRIEL WEATHERHEAD
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  226408. Templeton, J. L.B
  226409. Adv. Organomet. Chem.C
  226410. Mo /WM
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  226412. 2/28/96VJFour-electron alkyne ligands in molybdenum(II) and tungsten(II) complexes.W
  226413. 1989X
  226414. GABRIEL WEATHERHEAD
  226415. 17693
  226416. Tedder, J. M.B
  226417. TetrahedronC2PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALSM
  226418. 18702N
  226419. 2/28/96
  226420. The Importance of Polarity, Bond Strength, and Steric Factors in Determining the Site of Attack and  the Rate of Free Radical Substitution in Aliphatic Compounds.W
  226421. 1982X
  226422. GABRIEL WEATHERHEAD
  226423. 17694
  226424. Tedder, J. M.B
  226425. Angew. Chem., Int. Ed. Engl.C\PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /MECHANISMS /RADICAL SUBSTITUTION  /RADICAL ADDITIOM
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  226427. 2/28/96VqWhich Factors Determine the Reactivity and Regioselectivity of Free Radical Substitution and  Addition Reactions?W
  226428. 1982X
  226429. GABRIEL WEATHERHEAD
  226430. 17695
  226431. Tedder, J. M.//Walton, J. C.B
  226432. TetrahedronCRPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /ALKENES /C=C /RADICAL ADDITIONM
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  226435. The Importance of Polarity and Steric Effects in Determining the Rate and Orientation of Free Radical Addition to Olefins. Rules for Determining the Rate and Preferred Orientation.W
  226436. 1980X
  226437. GABRIEL WEATHERHEAD
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  226439. Taylor, S. K.B
  226440. Org. Prep. Proced. Int.M
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  226442. 2/28/96
  226443. V:Biosynthetic, biomimetic and related epoxide cyclizations.W
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  226445. GABRIEL WEATHERHEAD
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  226447. Ticcio, M.B    SynthesisC
  226448. FUNCTIONAL GROUPS /PROTECTION /HYDROXYL /ROR /ArOR /RSR /RSeR /ETHERS /SULFIDES /SELENIDES /ArSeR /ArSR  /CLEAVAGE /PROTECTION /DEPROTECTION /C-X /OH /C-X /SH /C-X /SeH /ArSH /ArOH /ArSeH  /PHENOLS /THIOLS /SELENOLS /S /SeM
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  226450. 2/28/96VFSelective Cleavage of Aryl Alkyl Ethers, Thioethers, and Selenoethers.W
  226451. 1988X
  226452. GABRIEL WEATHERHEAD
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  226454. Thurston, D. E.//Bose, D. S.B
  226455. Chem. Rev.M
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  226457. 2/28/96V@Synthesis of DNA-Interactive Pyrrolo[2,1-c][1,4]benzodiazepines.W
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  226460. GABRIEL WEATHERHEAD
  226461. 17699
  226462. Thummel, R. P.B
  226463. SynlettM
  226464. 18708N
  226465. 2/28/96ViThe application of Friedlander and Fischer methodologies to the synthesis of organized polyaza  cavities.W
  226466. 1992X
  226467. GABRIEL WEATHERHEAD
  226468. 17700
  226469. Thummel, R. P.B
  226470. TetrahedronM
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  226472. 2/28/96
  226473. VJThe synthesis and properties of organized polyaza cavity-shaped molecules.W
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  226475. GABRIEL WEATHERHEAD
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  226477. Thummel, R. P.B
  226478. Acc. Chem. Res.CNC-C BOND FORMATION /ANNULATIONS /4-RING /CYCLOBUTENE /CARBRING /4 /CYCLOBUTENEM
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  226480. 2/28/96V'Benzocyclobutene and Related Compounds.W
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  226482. GABRIEL WEATHERHEAD
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  226484. A Thompson, C. M.//Green, D. L. C.B
  226485. TetrahedronC4C-C BOND FORMATION /APPENDAGES /ENOLATES /ALKYLATIONM
  226486. 18711N
  226487. 2/28/96V%Recent advances in dianion chemistry.W
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  226490. GABRIEL WEATHERHEAD
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  226493. Chemtracts: Organic Che istryC
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  226495. 2/28/96V1Remote Asymmetric Induction Using Allylstannanes.W
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  226503. 2/28/96V6Landmarks in the Evolution of Heterogeneous Catalysts.W
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  226509. Acc. Chem. Res.M
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  226511. 2/28/96VVCytochalasan synthesis: macrocycle formation via intramolecular Diels-Alder reactions.W
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  226513. GABRIEL WEATHERHEAD
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  226515. Thiericke, R.//Rohr, J.B
  226516. Nat. Prod. Rep.M
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  226518. 2/28/96VQBiological variation of microbial metabolites by precursor-directed biosynthesis.W
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  226521. GABRIEL WEATHERHEAD
  226522. 17707
  226523. Thiem, J.//Klaffke, W.B
  226524. Top. Curr. Chem.M
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  226526. 2/28/96V$Syntheses of deoxy oligosaccharides.W
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  226533. 2/28/96V=Mechanisms Of Solvolytic Alkene-Forming Elimination-ReactionsW
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  226541. 2/28/96V[Reaction branching and extreme kinetic isotope effects in the study of reaction mechanisms.W
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  226543. GABRIEL WEATHERHEAD
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  226546. Acc. Chem. Res.C
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  226548. 2/28/96
  226549. V;Organochromium(III) chemistry: a neglected oxidation state.W
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  226555. 2/28/96V=The Synthesis and Transformations of Uronic Acid Nucleosides.W
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  226557. GABRIEL WEATHERHEAD
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  226561. 2/28/96V8Structural features and reactivity of tetrahalomethanes.W
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  226563. GABRIEL WEATHERHEAD
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  226565. A"Timofeeva, T. V.//Struchkov, Y. T.B Russ. Chem. Rev. (Engl. Transl.)C;ORGANOMETALLICS /GENERAL /PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  226567. 2/28/96VLThe conformational analysis of organoelemental and org nometallic molecules.W
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  226574. 2/28/96VTSequential transformations in organic chemistry: a synthetic strategy with a future.W
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  226581. 2/28/96VZThe use of selenium-containing intermediates to mediate or catalyze new organic reactions.W
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  226586. Tiecco, M.B
  226587. Acc. Chem. Res.CZPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /ARENES /SUBSTITUTION AROMATIC  /ARENESM
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  226589. 2/28/96V@Radical ipso Attack and ipso Substitution in Aromatic Compounds.W
  226590. 1980X
  226591. GABRIEL WEATHERHEAD
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  226593. Tidwell, T. T.B    SynthesisC-FUNCTIONAL GROUPS /OXIDATION /CH-OH TO C=O /SM
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  226595. 2/28/96VXOxidation of alcohols by activated  dimethyl sulfoxide and related reactions: an update.W
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  226597. GABRIEL WEATHERHEAD
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  226599. Tidwell, T. T.B
  226600. Org. React. (N.Y.)C-FUNCTIONAL GROUPS /OXID TION /CH-OH TO C=O /SM
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  226602. 2/28/96VrOxidation of alcohols to carbonyl compounds via alkoxysulfonium ylides: The Moffatt, Swern and  related reactions.W
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  226604. GABRIEL WEATHERHEAD
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  226606. Tidwell, T. T.B
  226607. Acc. Chem. Res.C0FUNCTIONAL GROUPS /PREPARATIONS /HETEROCUMULENESM
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  226609. 2/28/96V(Ketene chemistry: the second golden age.W
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  226611. GABRIEL WEATHERHEAD
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  226614. Angew. C em., Int. Ed. Engl.CJPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /CARBONIUM IONS /CARBOCATIONS /C+M
  226615. 18729N
  226616. 2/28/96V
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  226619. GABRIEL WEATHERHEAD
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  226621. Tidwell, T. T.B
  226622. TetrahedronC<PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULESM
  226623. 18730N
  226624. 2/28/96VKSterically Crowded Organic Molecules: Synthesis, Structure, and Properties.W
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  226630. 18731N
  226631. 2/28/96V%Glycals in enantiospecific synthesis.W
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  226633. GABRIEL WEATHERHEAD
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  226635. AXTolstikov, G. A.//Borisova, E. Y.//Cherkashin, M. I.//Komarov, V. M.//Arzamastsev, E. V.
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  226638. 2/28/96VcSynthesis and reactivity of N-substituted aminoamides, antiarrythmic and local anest etic activity.W
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  226640. GABRIEL WEATHERHEAD
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  226643. Chem. Rev.C8ORGANOMETALLICS /GENERAL /C-M /HETEROGENOUS CATALYSIS /PM
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  226645. 2/28/96V]Steric Effects of Phosphorus Ligands in Organometallic Chemistry and Heterogeneous Catalysis.W
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  226647. GABRIEL WEATHERHEAD
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  226649. Tolman, C. A.//McKinney, R. J.M
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  226651. 2/28/96a
  226652. GABRIEL WEATHERHEAD
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  226655. REAGENTS /SO2 /SM
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  226657. 2/28/96VBRecent Developments in Organic Synthesis in Liquid Sulfur Dioxide.W
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  226659. GABRIEL WEATHERHEAD
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  226664. 2/28/96VFNitrogen donors in organometallic chemistry and homogeneous catalysis.W
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  226667. GABRIEL WEATHERHEAD
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  226670. Au /V
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  226672. 2/28/96V
  226673. Cooperativity of chirality in homog neous catalysis: The gold(I)-catalyzed aldol reaction and the vanadium(IV)-catalyzed hetero  Diels-Alder cycloaddition.W
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  226675. GABRIEL WEATHERHEAD
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  226678. TetrahedronCDPHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICAL IONS /ION-RADICALSM
  226679. 18738N
  226680. 2/28/96V
  226681. Ion-Radical Organic Reactions.W
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  226683. 2771Y
  226684. GABRIEL WEATHERHEAD
  226685. 17730
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  226687. Org. React. (N.Y.)M
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  226689. 2/28/96V
  226690. The Wolff-Kishner Reduction.W
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  226692. GABRIEL WEATHERHEAD
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  226695. SynlettM
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  226698. Solid state organic reactions.W
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  226715. 2/28/96VFReaction control of guest compounds in host-guest inclusion complexes.W
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  226717. GABRIEL WEATHERHEAD
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  226723. 2/28/96V,3-Heteroquadricyclanes in Organic Synthesis.W
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  226726. GABRIEL WEATHERHEAD
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  226731. 2/28/96V!Advances in pyridazine chemistry.W
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  226733. GABRIEL WEATHERHEAD
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  226738. 2/28/96V
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  226760. 2/28/96VFTheoretical studies of the effects of hydration on organic equilibria.W
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  226772. 2/28/96V'Electrochemical Synthesis of Pyridines.W
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  226774. GABRIEL WEATHERHEAD
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  226779. 2/28/96VNEsterolytic reactivity in micellar assemblies and in cyclodextrin macrocycles.W
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  226781. GABRIEL WEATHERHEAD
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  226786. 2/28/96V7Asymmetric synthesis utilizing external chiral ligands.W
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  226793. 2/28/96V[Synthesis of pyrimidine derivatives and their related compounds using ketene dithioacetals.W
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  226810. ViCatalytic decomposition of diazomethane as a general method for the methylenation of chemical  compounds.W
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  226825. 2/28/96V]Genealogically directed synthesis: starburst/cascade dendrimers and hyperbranched structures.W
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  226832. 2/28/96VDThe synthesis of organochlorine compounds from one-carbon molecules.W
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  226860. C-C BOND FORMATION /APPENDAGES /DIASTEREOGENIC REACTIONS /STEREOCHEMISTRY /O=C-R  /C-M /REDUCTION 1,2-ADDITION (C=O, C-M) /X-C-C-Y /N, O /A INO ALCOHOLSM
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  226863. Stereoselective Synthesis of Diastereomeric Amino Alcohols from Chiral Aminocarbonyl Compounds  by Reduction or by Addition of Organometallic Reagents.W
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  226884. 2/28/96V?Enolisation of Simple Carbonyl Compounds and Related Reactions.W
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  226891. 2/28/96V]Recent progress in O-glycosylation methods and its application to natural products synthesis.W
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  226899. 2/28/96VYDynamic Stereochemistry of 5-, 6-, and 7-Membered Rings Using the Torsion Angle Notation.W
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  226909. GABRIEL WEATHERHEAD
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  226914. 2/28/96VNTransition metal templates as catalysts for selective organic transformations.W
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  226921. 2/28/96VDTransition metals and olefins. A promising land: a personal account.W
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  226936. 2/28/96V1Cyclopentanoids: A Challenge for New Methodology.W
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  226943. 2/28/96V@Transition-Metal Templates for Selectivity in Organic Synthesis.W
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  226980. 2/28/96V<Further deve opment of the ketoxime-based pyrrole synthesis.W
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  227026. -Keto Carboxylates, and Allyl Vinylic Carbonates Catalysed by Pd  Complexes.W
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  227034. 2/28/96VuNew General Synthetic Methods Involving  -Allylpalladium Complexes as Intermediates and Neutral  Reaction Conditions.W
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  227042. 2/28/96VRSynthetic Applications of the Palladium-Cat lysed Oxidation of Olefins to Ketones.W
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  227044. GABRIEL WEATHERHEAD
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  227047. Acc. Chem. Res.C
  227048. FUNCTIONAL GROUPS /TRANSFORMATIONS /CYCLOPROPANE CLEAVAGE /CYCLOADDITION /[3+2]  /CARBRING /3 /CYCLOPROPANES /ANNULATION 5-RING /RING CLEAVAGE /CARBRING /5  /CYCLOPENTANESM
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  227050. 2/28/96VGThermal Ring-Opening of Cyclopropyl Derivatives with Activated Olefins.W
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  227054. A    Tsuji, J.
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  227057. 2/28/96VAAddition Reactions of Butadiene Catalysed by Palladium Complexes.W
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  227059. GABRIEL WEATHERHEAD
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  227062. Adv. Heterocycl. Chem.C
  227063. PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /YLIDES /C-C BOND FORMATION /PERICYCLIC  REACTIONS /CYCLOADDITIONS /[3+2] /HETRING /5(N)M
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  227065. 2/28/96V.Recent advances in azomethine ylide chemistry.W
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  227067. GABRIEL WEATHERHEAD
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  227070. Adv. Carbohydr. Chem. Biochem.C
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  227072. 2/28/96V7Chemistry And Developments Of Fluorinated CarbohydratesW
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  227075. GABRIEL WEATHERHEAD
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  227077. A%Trzhtsinskaya, B. V.//Abramova, N. D.B
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  227080. 2/28/96V6Imidazole-2-thiones: synthesis, structure, properties.W
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  227082. GABRIEL WEATHERHEAD
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  227084. A*Truce, W. E.//Kreider, E. M.//Brand, W. W.B
  227085. Org. React. (N.Y.)
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  227088. 2/28/96V:The Smiles and Related Rearrangements of Aromatic Systems.W
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  227090. GABRIEL WEATHERHEAD
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  227095. 2/28/96V&The Gattermann Synthesis of Aldehydes.W
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  227097. GABRIEL WEATHERHEAD
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  227099. Trost, B. M.B
  227100. Acc. Chem. Res.CtORGANOMETALLICS /PALLADIUM /C-C BOND FORMATION /ANNULATIONS /5-RING /6-RING  /ANNULATION /5-RING,6-RING /C=C-C=C /PdM
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  227102. 2/28/96VGPalladium-catalyzed cycloisomerization of enynes and related reactions.W
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  227104. GABRIEL WEATHERHEAD
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  227107. Pure Appl. Chem.M
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  227109. 2/28/96V8Transition metal templates as guides for cycloadditions.W
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  227112. GABRIEL WEATHERHEAD
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  227114. Trost, B. M.//Merlic, C. A.B
  227115. C-C BOND FORMATION /APPENDAGES /ALKYLATION /FUNCTIONAL GROUPS /PREPARATIONS  /ORGANOSULPHUR COMPOUNDS /C=C-C-X /SO2 /SULPHONES /SUBSTITUTION /SO2 BY C /LEWIS  ACID CATALYSIS /NUCLEOPHILIC DISPLACEMENT /SM
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  227117. 2/28/96V)Sulfones: Substitution by C-Nucleophiles.W
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  227120. GABRIEL WEATHERHEAD
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  227123. SynlettM
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  227126. Direct polycondensation.W
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  227128. GABRIEL WEATHERHEAD
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  227130. Uchida, T.B    SynthesisC^C-C BOND FORMATION /HETEROANNULATIONS /MISCELLANEOUS /1 3-DIPOLAR /CYCLOADDITIONS /1,5-DIPOLARM
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  227132. 2/28/96V7Methods for the Construction of the Indolizine Nucleus.W
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  227134. GABRIEL WEATHERHEAD
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  227139. 2/28/96V#19-Electron organometallic adducts.W
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  227141. GABRIEL WEATHERHEAD
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  227144. Adv. Carbohydr. Chem. Biochem.C#PHYSICAL ORGANIC /STEREOELECTRONICSM
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  227147. V<Anomeric and exo-anomeric effects in carbohydrate chemistry.W
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  227153. Angew. Chem., Int. Ed. Engl.CGODDS AND ENDS /PHILOSOPHY OF SCIENCE /PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  227155. 2/28/96V8Geometric and Topological Thinking in Organic Chemistry.W
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  227157. GABRIEL WEATHERHEAD
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  227160. Acc. Chem. Res.CEC-C BOND FORMATION /ANNULATIONS /3-RING /CARBRING /3 /CYCLOP OPANONESM
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  227170. 2/28/96VNRecent advances in the use of enzyme-catalyzed reactions in organic synthesis.W
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  227176. Nat. Prod. Rep.M
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  227178. 2/28/96V*Steroids: reactions and partial syntheses.W
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  227185. Perfluoroalkyl(a yl)acetylenes.W
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  227193. 2/28/96V/sigma-Bonded Organic Derivatives of f Elements.W
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  227195. GABRIEL WEATHERHEAD
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  227198. Angew. Chem., Int. Ed. Engl.C+ORGANOMETALLICS /GENERAL /REARRANGEMENT /TMM
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  227200. 2/28/96V<Sigma,Pi-Rearrangements of Organotransition Metal Compounds.W
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  227211. GABRIEL WEATHERHEAD
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  227226. 2/28/96V|Transition-Metals In Organic-Synthesis - Hydroformylation, Reduction,  And Oxidation - Annual  Survey Covering The Year 1992W
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  227229. GABRIEL WEATHERHEAD
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  227234. 2/28/96VRMetalation and metal-assisted bond formation in  -electron deficient heterocycles.W
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  227242. 2/28/96VSMetallation and metal-assisted bond formation in  -electron deficient heterocycles.W
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  227258. 2/28/96V8Antisense oligonucleotides: a new therapeutic principle.W
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  227265. 2/28/96V\Antisense oligonucleotides: stereocontrolled synthesis of phosphorothioate oligonucleotides.W
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  227268. GABRIEL WEATHERHEAD
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  227274. 2/28/96V.Palladium-Catalysed Synthesis of Heterocycles.W
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  227289. 2/28/96V@Oligosaccharins - a new class of signalling molecules in plants.W
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  227297. 2/28/96V:Thioformyl compounds. Synthesis, structure and properties.W
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  227300. GABRIEL WEATHERHEAD
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  227304. 2/28/96V.The synthesis and properties of thioaldehydes.W
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  227306. GABRIEL WEATHERHEAD
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  227309. New Journal of ChemistryC
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  227313.     VlSynthetic approaches to homo- or heteropolynuclear pentahalophenyl palladium(II) or  platinum(II) complexes.W
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  227320. 2/28/96VAPrimary Nitro Compounds as a Source of Some Heterocyclic Systems.W
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  227328. 2/28/96VvCarbometalation: Addition of Organometallic Compounds to Isolated Multiple Bonds in Functionally  Substi uted Alkenes.W
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  227335. 2/28/96V$Catalytic Asymmetric DihydroxylationW
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  227343. 2/28/96V[Total Synthesis of Polycarbocyclic Sesquiterpenes. A Survey of Novel Methods and Reactions.W
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  227351. 2/28/96VXMetall macrocycles: Supramolecular Chemistry with Hard and Soft Metal Cations in Action.W
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  227357. Acc. Chem. Res.C=C-C BOND FORMATION /ANNULATIONS /MISCELLANEOUS /TRITERPENOIDSM
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  227359. 2/28/96VMBioorganic Chemistry: Total Synthesis of Tetra- and Polycyclic Triterpenoids.W
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  227364. Pure Appl. Chem.C
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  227368. Novel aspects of eta'-diiod ne coordination and diiodine oxidative addition to platinum(II) and halide transfer oxidation reactions  of organoplatinium(II) and CuIIX2.W
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  227376. 2/28/96VCTuning the reactivity of metals held in a rigid ligand environment.W
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  227384. 2/28/96V!Calixarenes, chemical chameleons.W
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  227391. 2/28/96VFSyntheses of 3-amino-2-azetidinones: a literature survey.  TetrahedronW
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  227399. 2/28/96VHThe SN(ANRORC) Mechanism: A New Mechanism for Nucleophilic Substitution.W
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  227406. 2/28/96VsCh mical modifications of aza sugars, inhibitors of N-glycoprotein-processing glycosidases and of HIV-I  infection.W
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  227414. 2/28/96V)The use of zeolit s in organic reactions.W
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  227421. 2/28/96VLSelective functionalization and conformational properties of calix[4]arenes.W
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  227435. 2/28/96Vh'Tert-amino effect' in heterocyclic synthesis. Ring closure reactions of  N,N-dialkyl-1,3-dien-1-amines.W
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  227437. GABRIEL WEATHERHEAD
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  227439. Verboom, W.//Reinhoudt, D. N.B
  227440. Bull. Soc. Chim. Fr.M
  227441. 18838N
  227442. 2/28/96VBFour-membered cyclic nitrones. Synthesis and reactivity: a review.W
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  227444. GABRIEL WEATHERHEAD
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  227446. Venepalli, B. R.//Agosta, W. C.B
  227447. Chem. Rev.C<PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /STRAINED MOLECULESM
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  227449. 2/28/96V6 Fenestranes and the Flattening of Tetrahedral Carbon.W
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  227451. GABRIEL WEATHERHEAD
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  227454. Adv. Organomet. Chem.M
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  227456. 2/28/96V4Alkyl- and aryl-substituted main-group metal amides.W
  227457. 1990X
  227458. GABRIEL WEATHERHEAD
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  227460. Veinberg, G. A.//Lukevics, E.B
  227461. HeterocyclesC
  227462. Si /SnM
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  227464. 2/28/96
  227465. VZOrganosilicon And Organotin Compounds In The Synthesis And  Transformation Of Beta-LactamsW
  227466. 1994X    2309-2342Y
  227467. GABRIEL WEATHERHEAD
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  227469. Vedejs, E.//West, F. G.B
  227470. Chem. Rev.CNC-C BOND FORMATION /ANNULATIONS /5-RING /YLIDES /2,3-DIPOLAR CYCLOADDITION /SiM
  227471. 18842N
  227472. 2/28/96V6Ylides by the Desilyl tion of alpha-Silyl Onium Salts.W
  227473. 1986X
  227474. GABRIEL WEATHERHEAD
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  227476. Vedejs, E.B
  227477. Acc. Chem. Res.C2C-C BOND FORMATION /ANNULATIONS /RING EXPANSION /SM
  227478. 18843N
  227479. 2/28/96V3Sulfur-Mediated Ring Expansions in Total Synthesis.W
  227480. 1984X
  227481. GABRIEL WEATHERHEAD
  227482. 17835
  227483. Vedejs, E.//Krafft, G. A.B
  227484. TetrahedronCjC-C BOND FORMATION /ANNULATIONS /RING EXPANSION /CONTRACTION /C-X /SR /CYCLIC  SULFIDES /RING EXPANSION /SM
  227485. 18844N
  227486. 2/28/96V%Cyclic Sulfides in Organic Synthesis.W
  227487. 1982X
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  227489. GABRIEL WEATHERHEAD
  227490. 17836
  227491. Vedejs, E.B
  227492. Org. React. (N.Y.)
  227493. !C_FUNCTIONAL GROUPS /DISSOLVING METAL /O=C-Ar /KETONES /REDUCTION /CLEMMENSEN /Ar-C  /ALKYLA ENESM
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  227495. 2/28/96V>Clemmensen Reduction of Ketones in Anhydrous Organic Solvents.W
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  227497. GABRIEL WEATHERHEAD
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  227500. Top. Stereochem.M
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  227502. 2/28/96V5Stereochemistry and mechanism in the Wittig reaction.W
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  227505. GABRIEL WEATHERHEAD
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  227507. Vasella, A.B
  227508. Pure Appl. Chem.M
  227509. 18847N
  227510. 2/28/96V.A new approach to the synthesis of glycosides.W
  227511. 1993X
  227512. 731-52Y
  227513. GABRIEL WEATHERHEAD
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  227515. $A"Vase la, A.//Baudin, G.//Panza, L.B
  227516. Heteroatom ChemistryC
  227517. 18848N
  227518. 2/28/96V9Synthesis of glycosyl phosphonates and related compounds.W
  227519. 1991X
  227520. GABRIEL WEATHERHEAD
  227521. 17840
  227522. Varvoglis, A.B    SynthesisC-REAGENTS /HALOGENATION OXIDATION ARYLATION /IM
  227523. 18849N
  227524. 2/28/96V1Polyvalent Iodine Compounds in Organic Synthesis.W
  227525. 1984X
  227526. GABRIEL WEATHERHEAD
  227527. 17841
  227528. Varma, R. S.B
  227529. Synlett
  227530. 18850N
  227531. 2/28/96V=Synthesis of oligonucleotide analogs with modified backbones.W
  227532. 1993X
  227533. 621-37a
  227534. GABRIEL WEATHERHEAD
  227535. 17842
  227536. 'A4Varfolomeev, S. D.//Rainina, E. I.//Lozinskii, V. I.B
  227537. Pure Appl. Chem.M
  227538. 18851N
  227539. 2/28/96V7Cryoimmobilized enzymes and cells in organic synthesis.W
  227540. 1992X
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  227542. GABRIEL WEATHERHEAD
  227543. 17843
  227544. (A    Vogel, E.B
  227545. Pure Appl. Chem.M
  227546. 18852N
  227547. 2/28/96V9The porphyrins from the 'annulene chemist's' perspective.W
  227548. 1993X
  227549. 143-52Y
  227550. GABRIEL WEATHERHEAD
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  227553. SynlettM
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  227555. 2/28/96V]Optically Pure 7-Oxabicyclo[2.2.1]hept-5-en-2-yl Derivatives ('Naked Sugars') as New Chirons.W
  227556. 1990X
  227557. GABRIEL WEATHERHEAD
  227558. 17845
  227559. *A    Vogel, E.B
  227560. Pure Appl. Chem.M
  227561. 18854N
  227562. 2/28/96V
  227563. Novel porphyrinoids.W
  227564. 1990X
  227565. GABRIEL WEATHERHEAD
  227566. 17846
  227567. Vogel, H.-H.B    SynthesisCQC-C BOND FORMATION /APPENDAGES /1,2-ADDITION /C=C /RADICAL ADDITION /H-C-C-C-COORM
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  227569. 2/28/96
  227570. +V_Radical Addition of Carboxylic Acid Derivatives to Unsaturated Compounds as a Synthetic Method.W
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  227572. GABRIEL WEATHERHEAD
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  227575. Angew. Chem., Int. Ed. Engl.M
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  227577. 2/28/96VjPigments for visual differentiation of enantiomers: crown ethers as optical sensors for chiral  compounds.W
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  227579. GABRIEL WEATHERHEAD
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  227582. J. F uorine Chem.C
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  227584. 2/28/96VbFluoride ion as a nucleophile and a leaving group in aromatic nucleophilic substitution reactions.W
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  227587. GABRIEL WEATHERHEAD
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  227590. Adv. Heterocycl. Chem.M
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  227592. 2/28/96V3Ring transformations of five-membered heterocycles.W
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  227594. GABRIEL WEATHERHEAD
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  227599. 2/28/96V<Intramolecular Pericyclic Reactions of  cetylenic Compounds.W
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  227606. 2/28/96VWThe mechanism of the dehydration of alcohols and hydration of alkenes in acid solution.W
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  227610. 1A'Viehe, H. G.//Merenyi, R.//Janousek, Z.B
  227611. Pure Appl. Chem.C2PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALSM
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  227613. 2/28/96V5Captodative Substituent Effects in Radical Chemistry.W
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  227621. 2/28/96VKThe Chemistry of Dichloromethyleneammonium Salts ('Phosgenammonium Salts').W
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  227623. GABRIEL WEATHERHEAD
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  227625. Viehe, H. G.B
  227626. Angew. Chem., Int. Ed. Engl.CMFUNCTIONAL GROUPS /PREPARATIONS /ALKYNES /C=C-X /N /ALKYNYLAMINES /ACETYLENESM
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  227630. GABRIEL WEATHERHEAD
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  227664. 2/28/96V"Cobalt-Mediated Steroid Synthesis.W
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  227670. Angew. Chem., Int. Ed. Engl.CwC-C BOND FORMATION /AROMATICS /RING FORMATION /ORGANOMETALLICS /COBALT  /CYCLOADDITION /[2+2+2] /CARBRING /6 ARENES /CoM
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  227672. 2/28/96VFCobalt-mediated [2+2+2] Cycloadditions. A Maturing Synthetic Strategy.W
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  227674. GABRIEL WEATHERHEAD
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  227679. 2/28/96V6Chemical Reaction in Molten Salts and their Reactions.W
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  227685. 2/28/96V6Synthesis and Reactions of alpha-Hydroxylamino oximes.W
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  227687. GABRIEL WEATHERHEAD
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  227700. 2/28/96VDCurrent state of organocobalt (IV) and organorhodium (IV) chemistry.W
  227701. 1985X
  227702. GABRIEL WEATHERHEAD
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  227704. Vogtle, F.//Neumann, P.B    SynthesisC.C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGEM
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  227707. The Synthesis of [2.2] Phanes.W
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  227709. GABRIEL WEATHERHEAD
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  227712. Acc. Chem. Res.C2PHOTOCHEMISTRY /REACTIVE INTERMEDIATES /BIRADICALSM
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  227714. 2/28/96Vh1,5-Biradicals and five-membered rings generated by delta-hydrogen abstraction in photoexcited  ketones.W
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  227716. GABRIEL WEATHERHEAD
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  227719. Org. React. (N.Y.)C
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  227722. 2/28/96
  227723. @V7Synt etic Applications of Phosphoryl-Stabilised Anions.W
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  227725. GABRIEL WEATHERHEAD
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  227730. 2/28/96VNBenzene and its derivatives as bridging ligands in transition metal complexes.W
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  227747. 2/28/96V9Advances in the chemistry of heterodiene metal complexes.W
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  227769. 2/28/96V/Advances in amination of nitrogen heterocycles.W
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  227774. HeterocyclesC
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  227777. 2/28/96V-Carbon-Substitution of Nitrogen Heterocycles.W
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  227785. 2/28/96VDThe Functional Group Selectivity of Complex Hydride Reducing Agents.W
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  227800. 2/28/96V$Enzymic Protecting Group Techniques.W
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  227808. 2/28/96VEAmino acid esters as chiral auxiliaries in asymmetric cycloadditions.W
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  227816. 2/28/96VLMechanism of Grignard reagent formation. The surface nature of the reaction.W
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  227827. GABRIEL WEATHERHEAD
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  227830. TetrahedronC!PHYSICAL ORGANIC /STEREOCHEMISTRYM
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  227841. 2/28/96V)Photoisomerization dynamics of stilbenes.W
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  227890. 2/28/96V%Fluorination by Sulfur Tetrafluoride.W
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  228731. V,Alkali Metal Fluorides in Organic Synthesis.W
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  228733. GABRIEL WEATHERHEAD
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  228738. 2/28/96VDAntimony Pentahalides as Catalysts of Friedel-Crafts Type Reactions.W
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  228742. Yakobson, G. G.//Vlasov, V. M.B    SynthesisCIC-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION /Ar-X /F /FLUORIDESM
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  228744. 2/28/96V:Recent Synthetic Methods for Polyfluoroaromatic Compounds.W
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  228757. 2/28/96V7Pseudomonas fluorescens lipase in asymmetric synthesis.W
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  228772. 2/28/96V"Asymmetric Catalysis by Alkaloids.W
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  228780. The Reimer-Tiemann Reaction.W
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  228787. 2/28/96V^The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroida.W
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  228802. P /SiM
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  228812. 2/28/96V4Substitution and Addition Reactions of Thiocyanogen.W
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  228844. 2/28/96VUReactions of the eta-5-pyrrolyl ligand: A new challenge in the chemistry of pyrroles.W
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  229070. 2/28/96V!The synthesis of brassinosteroid.W
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  229667. 2/28/96V1Electron Transfer Reactions in Organic Chemistry.W
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  229709. 2/28/96V'Handbook of Organophosphorus Chemistry.W
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  229724. 2/28/96V(Biotransform tions in Organic Chemistry.W
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  229739. 19142N
  229740. 2/28/96V
  229741. Photoinduced Electron Transfer.W
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  229743. GABRIEL WEATHERHEADy    Amsterdam
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  229748. 2/28/96
  229749. KV#Dienes in the Diels-Alder Reaction.W
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  229751. GABRIEL WEATHERHEADy
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  229755. TARGET SYNTHESIS /MISCELLANEOUSK
  229756.  de Gruyter, W.M
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  229771. 2/28/96V8Organic Synthesis: Concepts, Methods, Starting MaterialsW
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  229773. GABRIEL WEATHERHEADy
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  229777. Harwood Academic Publ.M
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  229779. 2/28/96V;Synthetic Aspects of the Fluorination of Organic Compounds.W
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  229788. Heterocyclic Chemistry.W
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  229790. GABRIEL WEATHERHEADy
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  229796. 2/28/96V'Essentials of Molecular Photochemistry.W
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  229798. GABRIEL WEATHERHEADy
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  229802. Gordon and BreachM
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  229804. 2/28/96V=Phase Transfer Catalysis. Selected Problems and Applications.W
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  229806. GABRIEL WEATHERHEADy
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  229810. Royal Society of ChemistryM
  229811. 19151N
  229812. 2/28/96V
  229813. Crown Ethers and Cryptands.W
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  229815. GABRIEL WEATHERHEADy
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  229821. 2/28/96V#Synthetic Peptides: A User's Guide.W
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  229829. 2/28/96V'Protective Groups in Organic Synthesis.W
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  229854. Methods for the Oxidation of Organic Compounds: Alcohols, Alcohol Derivatives, Alkyl Halides,  Nitroalkanes, Alkyl Azides, Carbonyl Compounds, Hydroxyarenes, and Aminoarenes.W
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  229876. 2/28/96V%Transition Metals in Total Synthesis.W
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  229884. 2/28/96V'The Chemistry of the Metal-Carbon Bond.W
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  229892. 2/28/96V!Polycyclic Aromatic Hydrocarbons.W
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  229900. 2/28/96V;Medical, Biochemical, and Chemical Aspect of Free Radicals.W
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  229928. 2/28/96V&Ring Enlargement in Organic Chemistry.W
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  229936. 2/28/96VnAminomethylenemalonates and their use in Heterocyclic Synthesis (Advances in Heterocyclic C emistry, Vol. 54).W
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  229966. Tactics of Organic Synthesis.W
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  229974. 2/28/96V/Heterolytic Fragmentation of Organic Molecules.W
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  229982. 2/28/96VDEnantiosele tive Synthesis of Natural Products from Chiral Terpenes.W
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  230000. Polarity Control for Synthesis.W
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  230023. 2/28/96V)Organic Synthesis with Oxidative Enzymes.W
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  230030. 2/28/96VVCyclitols and Their Derivatives: A Handhook of Physical, Spectral, and Synthetic Data.W
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  230038. 2/28/96V Lanthanides in Organic SynthesisW
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  230087. 2/28/96VFStereo-Differentiating Reactions - The Nature of Asymmetric Reactions.W
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  230094. 2/28/96V/Electrophilic Substitution of Organomercurials.W
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  230116. Clarendon PressM
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  230118. 2/28/96V#The Chemical Synthesis of Peptides.W
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  230127. Quinolines.W
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  230159. 2/28/96V4Organic Photochemistry. Principles and Applications.W
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  231515. 2/28/96V5Phosphoranylideneketene, -Thioketene and -KeteniminesW
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  231531. Georg Thieme VerlagM
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  231540. Georg Thieme VerlagM
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  231543. Cross-Conjugated Systems of Cycloheptatrienes: Tropenes, Tropolenes, Heptafulvenes,  Heptafulvalenes, Higher Vinylogues of HeptafulvenesX
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  231563. GABRIEL WEATHERHEADy
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  231567. Gas - Phase Metal ReactionsK
  231568. ElsevierM
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  231570. 2/28/96V;Comparison of Main Group and Transition Metal Ion ChemistryW
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  231573. GABRIEL WEATHERHEADy    Amsterdam
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  231576. Petrarch SystemsM
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  231578. 2/28/96V Silane coupling agent chemistry.W
  231579. 1987X
  231580. GABRIEL WEATHERHEADy
  231581. Bristol, PA
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  231584. Carbenes (Carbenoids)K
  231585. Georg Thieme VerlagM
  231586. 19365N
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  231588. 1989X
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  231594. WileyM
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  231599. GABRIEL WEATHERHEADy
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  231619. Toxicity of Heterocycles.W
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  231625.  eorg Thieme VerlagM
  231626. 19370N
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  231633. Georg Thieme VerlagM
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  231636. Aldehydes: General IntroductionW
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  231645. 0V>Dicarbonic Derivatives with Two Simple Carbonic Acid FunctionsW
  231646. 1983X    1000-1202Y
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  231657. Oxford
  231658. 18365
  231659. Klamann, D.//Hagemann, H.B1Organic Nitrogen Compounds with a C,N-Double BondK
  231660. Georg Thieme VerlagM
  231661. 19374N
  231662. 2/28/96V
  231663. Diazo CompoundsW
  231664. 1990X
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  231666. E14ba
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  231669. Trost, B. M.//Fleming, I.B
  231670. Comprehensive Organic SynthesisCVFUNCTIONAL GROUPS /OXIDATION /ALKENES AND ALKYNES /EPOXIDATION /EPOXIDE HETRING  /3(O)K
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  231673. 2/28/96V"Epoxidation and Related Processes.W
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  231677. 18367
  231678. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic Chemistry
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  231680. Pergamon PressM
  231681. 19376N
  231682. 2/28/96V;Heterocyclic Rings containing Arsenic, Antimony or Bismuth.W
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  231684. GABRIEL WEATHERHEADy
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  231688. Organic Nitrogen Compounds IIK
  231689. Georg Thieme VerlagM
  231690. 19377N
  231691. 2/28/96V;3-Oxo-, 3-Imino-1,2-oxazetidines and 2-Oxo-1,3-OxazetidinesW
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  231700. 2/28/96VS3-Oxo-1,2-diazetidines, 2-Oxo- and 2,4-Dioxo-1,3-diazetidines and Their DerivativesW
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  231707. 19379N
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  231715. Organic Nitrogen Compounds IIK
  231716. Georg Thieme VerlagM
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  231720. 1991X
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  231726. Organic Nitrogen Compounds IIK
  231727. Georg Thieme VerlagM
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  231738. Organic Nitrogen Compounds IIK
  231739. Georg Thieme VerlagM
  231740. 19382N
  231741. 2/28/96V*3-Oxo- and  -Imino-1,2-thiazedine 1-OxidesW
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  231743. E16ba
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  231748. Georg Thieme VerlagM
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  231750. 2/28/96V
  231751. 3-Oxo- and 3-IminodiaziridinesW
  231752. 1991X
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  231758. Organic Nitrogen Compounds IIK
  231759. Georg Thieme VerlagM
  231760. 19384N
  231761. 2/28/96V)2,3-Dioxoazetidines and Their DerivativesW
  231762. 1991X
  231763. 868-882Y
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  231768. Carbenes (Carbenoids)K
  231769. Georg Thieme VerlagM
  231770. 19385
  231771. 2/28/96V5Carbenes with Coordination Number 2: CycloalkylidenesW
  231772. 1989X
  231773. 391-606Y
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  231778. Organic Nitrogen Compounds IIIK
  231779. Georg Thieme VerlagM
  231780. 19386N
  231781. 2/28/96V
  231782. AziridinesW
  231783. 1 92X
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  231793. 1989Z
  231794. GABRIEL WEATHERHEADy
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  231796. 18379
  231797. Schaumann, E.B
  231798. Heteroarenes III, Part 3K
  231799. Georg Thieme VerlagM
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  231801. 2/28/96V
  231802. BenzimidazolesW
  231803. 1994X
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  231805. GABRIEL WEATHERHEADy    Stuttgart
  231806. 18380
  231807. Kreher, R. P.B
  231808. Heteroarenes I, Part 1K
  231809. Georg Thieme VerlagM
  231810. 19389N
  231811. 2/28/96V
  231812. DibenzofuransW
  231813. 1994X
  231814. 799-866Y
  231815. GABRIEL WEATHERHEADy    Stuttgart
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  231817. Hanack, M.B
  231818. CarbanionsK
  231819. Georg Thieme VerlagM
  231820. 19390N
  231821. 2/28/96V
  231822. 1-Alkynyl AnionsW
  231823. 114- 70Y
  231824. E19da
  231825. GABRIEL WEATHERHEADy    Stuttgart
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  231827. Hanack, M.B
  231828. CarbanionsK
  231829. Georg Thieme VerlagM
  231830. 19391N
  231831. 2/28/96V"alpha-Metal Substituted CarbanionsW
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  231834. E19da
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  231838. Organic Nitrogen Compounds IIIK
  231839. Georg Thieme VerlagM
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  231842. AzirinesW
  231843. 1992X
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  231849. Organic Nitrogen Compounds IIIK
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  231854. 1992X
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  231870. Organic Nitrogen Compounds IIK
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  231880. Georg Thieme VerlagM
  231881. 19396N
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  231884. 1991X
  231885. 915-922Y
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  231889. Tros , B. M.//Fleming, I.B
  231890. Comprehensive Organic SynthesisC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[2+2]K
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  231893. 2/28/96V#Thermal Cyclobutane Ring Formation.W
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  231897. 18389
  231898. Kropf, H.//Schaumann, E.B
  231899. Ene,X and Yne,X-CompoundsK
  231900. Georg Thieme VerlagM
  231901. 19398N
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  231903. Ketene AcetalsW
  231904. 1993X    1598-2352Y
  231905. GABRIEL WEATHERHEADy    Stuttgart
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  231910. 2/28/96V!alpha,beta-Unsaturated Carbonyls.W
  231911. 1983X
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  231914. 18391
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  231917. 19400N
  231918. 2/28/96V Electrolytic Reductive Coupling.W
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  231930. 18393
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  231935. 1994Z
  231936. GABRIEL WEATHERHEADy
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  231939. German, L.//Zemskov, S.C
  231940. F /Xe /XeF2K
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  231942. 19403N
  231943. 2/28/96V?Xenon difluoride.  New Fluorinating Agents in Organic SynthesisW
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  231952. 2/28/96VWStereocontrolled syntheses of P-chiral analogues of nucleoside cyclic 3',5'-phosphates.W
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  231965. Morrison, J. D.B>Asymmetric Synthesis. Stereodifferentiating Reactions, Part B.CdC-C BOND FORMATION /ANNULATIONS /6-RING /ALKENES /C=C /ANNULATION /6-RING  /CYCLISATION /CARBRING /6K
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  231967. 2/28/96V;Olefin Cyclisation Processes That Form Carbon-Carbon Bonds.W
  231968. 1984X
  231969. GABRIEL WEATHERHEADy
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  231971. 18398
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  231974. 19407N
  231975. 2/28/96V?Olefin Cyclisation Processes That Form Carbon-Heteroatom Bonds.W
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  231978. New York
  231979. 18399
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  231981. Academic PressM
  231982. 19408N
  231983. 2/28/96V;Redox Glycosidation: a Stereoselective Synthesis of SucroseW
  231984. 1991X
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  231986. GABRIEL WEATHERHEADy
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  231988. 18400
  231989. Trost, B. M.//Fleming, I.B
  231990. Comprehensive Organic SynthesisC
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  231992. Pergamon PressM
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  231994. 2/28/96VHReduction of Carboxylic Acid Derivatives to Alcohols, Ethers and Amines.W
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  231998. 18401
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  232000. Jai Press IncM
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  232008. 18402
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  232010. Geor  Thieme VerlagM
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  232016. GABRIEL WEATHERHEADy    Stuttgart
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  232020. 19412N
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  232022. Thiocarboxylic Acid AmidesW
  232023. 1985X    1218-1303Y
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  232035. Georg Thieme VerlagM
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  232038. Thiocarboxylic S-EstersW
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  232057. GABRIEL WEATHERHEADy
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  232061. Organic Nitrogen Compounds IIIK
  232062. Georg Thieme VerlagM
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  232072. Georg Thieme VerlagM
  232073. 19418N
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  232081. Georg Thieme VerlagM
  232082. 19419N
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  232085. 1992X
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  232094. 2/28/96VLApplications of intramolecular 2+2 photocycloadditions in organic synthesis.W
  232095. 1989Z
  232096. GABRIEL WEATHERHEADy
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  232100. Carbocyclic pi-Electron SystemsK
  232101. Georg Thieme VerlagM
  232102. 19421N
  232103. 2/28/96V.Cross-Conjugated Systems of CyclononatetraenesW
  232104. 1985X
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  232110. 2/28/96V    HeptaleneW
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  232116. Georg Thieme VerlagM
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  232119. Pleiadienes and AcepleiadienesW
  232120. 1985X
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  232126. Carbocyclic pi-Electron SystemsK
  232127. Georg Thieme VerlagM
  232128. 19424N
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  232131. 1985X
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  232137. Carbocyclic pi-Electron SystemsK
  232138. Georg Thieme VerlagM
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  232141. Cyclopropenylium CationsW
  232142. 1985X
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  232146. 18417
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  232148. Carbocyclic pi-Electron SystemsK
  232149. Georg Thieme VerlagM
  232150. 19426N
  232151. 2/28/96V
  232152. Cross-Conjugated Systems of Cyclopro enes: Cyclopropenones, Cyclopropenethiones and -Selenones, Cyclopropenimines, Triafulvalenes,  Calicenes, Heptatriafulvenes, QuinocyclopropenesW
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  232159. Carbocyclic pi-Electron SystemsK
  232160. Georg Thieme VerlagM
  232161. 19427N
  232162. 2/28/96V
  232163. Cross-Conjugated Systems of Cyclopentadiones: 6-Heteropentafulvenes, Pentafulvenes,  Pentafulvalenes and Their Vinylogues, Heteroanalogues of Sesquifulvalenes, Sesquifulvalenes and Their  VinyloguesW
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  232169. Kreher, R. P.B
  232170. Heteroarenes I, Part 2K
  232171. Georg Thieme VerlagM
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  232174. Ind lizinesW
  232175. 1994X
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  232177. GABRIEL WEATHERHEADy    Stuttgart
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  232180. Organic Nitrogen Compounds IVK
  232181. Georg Thieme VerlagM
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  232184. Nitro CompoundsW
  232185. 1992X
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  232187. E16da
  232188. GABRIEL WEATHERHEADy    Stuttgart
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  232191. Organic Nitrogen Compounds IIIK
  232192. Georg Thieme VerlagM
  232193. 19430N
  232194. 2/28/96V>Organic Nitrites and Carboxylic Ac d / Nitrous Acid AnhydridesW
  232195. 1992X
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  232201. Organic Nitrogen Compounds IIIK
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  232229. Trost, B. M.//Fleming, I.B
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  232239. Georg Thieme VerlagM
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  232299. 2/28/96V Synthesis of Phosphonium Ylides.W
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  232303. 18434
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  232322. Georg Thieme VerlagM
  232323. 19445N
  232324. 2/28/96V0Catalytic Reactions: Metathesis and CometathesisW
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  232329. Georg Thieme VerlagM
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  232359. 1984X
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  232362. 18441
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  232364. PYRROLES /FURANS /THIOPHENES /SELENO HENES /TELLUROPHENES /INDOLES /CARBAZOLES /ISOINDOLES /INDOLIZINES /BENZOFURANES  /BENZOFURANES /BENZOTHIOPHENES /PYRROLENINES /INDOLENINES /PYRROLINES /PYRROLIDINESK
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  232368. 1984X
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  232373. PYRROLES /FURANS /THIOPHENES /SELENOPHENES /TELLUROPHENES /INDOLES /CARBAZOLES  /ISOINDOLES /INDOLIZINES /BENZOFURANES /BENZOFURANES /BENZOTHIOPHENES /PYRROLENINES  /INDOLENINES /PYRROLINES /PYRROLIDINESK
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  232380. 18443
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  232384. 19452N
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  232386. 1984X
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  232389. 18444
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  232401. Rev. Heteroatom Chem.C
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  232417. 1984X
  232418. GABRIEL WEATHERHEADy
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  232420. 18447
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  232422. Organophosphorus Compounds IK
  232423. Georg Thieme VerlagM
  232424. 19456N
  232425. 2/28/96V\Phosphorus(III) Compounds with Coordination Number 3: Phosphorous Acis and Their DerivativesW
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  232432. Georg Thieme VerlagM
  232433. 19457N
  232434. 2/28/96V(Alkylperoxy Esters of Inorganic OxyacidsW
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  232441. Georg Thieme VerlagM
  232442. 19458N
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  232451. Georg Thieme VerlagM
  232452. 19459N
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  232454. VSInorganic Phosphorus, Arsenic, Antimony and Bismuth Compounds as Oxidation ReagentsW
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  232458. GABRIEL WEATHERHEADy    Stuttgart
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  232462. Georg Thieme VerlagM
  232463. 19460N
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  232470. Trost, B. M.//Fleming, I.B
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  232482. Jai Press, Inc.M
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  232484. 2/28/96V
  232485. Thermal Reaction of Cyclopropanone Ketals. Scope and Applications of the Cycloa dition Reactions of Cyclopropanone Ketals and  -Delocalized Vinyl Carbenes...W
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  232492. Pergamon PressM
  232493. 19463N
  232494. 2/28/96VHRecent Applications of the Inverse Electron Demand Diels-Alder Reaction.W
  232495. 1989Z
  232496. GABRIEL WEATHERHEADy
  232497. Oxford, U.K.
  232498. 18455
  232499. Lindberg, T.B,Strategies and Tactics in Org nic Synthesis.K
  232500. Academic PressM
  232501. 19464N
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  232503. Diels-Alder Reactions of Heterocyclic Azadienes: Development of a Strategy for the Total Synthesis  of Streptonigrin, Lavendamycin and Synthetic Quinoline-5,8-quinones.W
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  232505. GABRIEL WEATHERHEAD
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  232508. Academic PressM
  232509. 19465N
  232510. 2/28/96V
  232511. Solution of Complex Stereochemical Problems with the Aid of Molecular Mechanics-based Modeling:  an Application to the Total Synthesis of (
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  232513. 1991X
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  232538. Georg Thieme VerlagM
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  232664. 19482N
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  232681. Georg Thieme VerlagM
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  232688. GABRIEL WEATHERHEADy    Stuttgart
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  232692. Georg Thieme VerlagM
  232693. 19485N
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  232702. 19486N
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  232711. Georg Thieme VerlagM
  232712. 19487N
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  232731. Georg Thieme Verlag
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  232747. 18482
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  232750. Georg Thieme VerlagM
  232751. 19491N
  232752. 2/28/96V=Carbenes with Coordination Nu ber 2: (2+x)-CycloalkenylidenesW
  232753. 1989X
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  232756. GABRIEL WEATHERHEADy    Stuttgart
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  232760. Georg Thieme VerlagM
  232761. 19492N
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  232766. GABRIEL WEATHERHEADy    Stuttgart
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  232796. 18487
  232797. Tr st, B. M.//Fleming, I.B
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  232800. 19496N
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  232802. Acyloin Coupling Reactions.W
  232803. 1991X
  232804. GABRIEL WEATHERHEADy
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  232806. 18488
  232807. Trost, B. M.//Fleming, I.B
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  232809. C+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  232823. GABRIEL WEATHERHEADy
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  232825. 18490
  232826. Mayo, P. D.B,Rearrangements in Ground and Excited States.C0ORGANOMETALLICS /SILICON /C-M /Si /REARRANGEMENTK
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  232848. GABRIEL WEATHERHEADy
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  232850. 18493
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  232855. 1984a
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  232859. Asymmetric SynthesisC
  232860. C-C BOND FORMATION /APPEND GES /ENANTIOGENIC REACTIONS /ORGANOMETALLICS /BORON /C=C /ALKENES /BORANES  /HYDROBORATION /HYDROMETALLATION /B /ENANTIOSELECTIVE /C-OHK
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  232863. Asymmetric Hydroboration.W
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  232876. 18496
  232877. Hudlicky, T.B)Organic Synthesis-Theory and ApplicationsK    Jai PressM
  232878. 19505N
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  232887. 19506N
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  232889. Oxidation by Microbial Methods.W
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  232893. 18498
  232894. Mayo, P. D.B,Rearrangements in Ground and Excited States.CAPHYSICAL ORGANIC /REARRANGEMENTS /PHOTOCHEMICAL REACTIONS /ARENESK
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  232900. 18499
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  232908. GABRIEL WEATHERHEADy    Stuttgart
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  232918. 18501
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  232920. ORGANOMETALLICS /TMK
  232921. SpringerM
  232922. 19510N
  232923. 2/28/96V
  232924. Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts  and Transition Metal Compounds.W
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  233072. Georg Thieme VerlagM
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  233075. 1,3-Dithiolium SaltsW
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  233083. Royal Society of ChemistryM
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  233102. GABRIEL WEATHERHEADy
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  234033. Jai Pres , Inc.M
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  234037. GABRIEL WEATHERHEADy
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  234041. VCH PublishersM
  234042. 19635N
  234043. 2/28/96VFThe Electrocyclic Ring Opening of Fluorinated Cyclobutene Derivatives.W
  234044. 1988a
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  234046. New York
  234047. 18627
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  234049. Organic Peroxy CompoundsK
  234050. Georg Thieme VerlagM
  234051. 19636N
  234052. 2/28/96V
  234053. Acyl Alkyl PeroxidesW
  234054. 1988X
  234055. 794-855Y
  234056. GABRIEL WEATHERHEADy    Stuttgart
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  234058. Oae, S.B
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  234061. 19637N
  234062. 2/28/96V)Explorations into chalcogen heterocycles.W
  234063. 1989Z
  234064. GABRIEL WEATHERHEADy
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  234066. 18629
  234067. Katritzky, A. RB$Comprehensive Heterocyclic ChemistryM
  234068. 19638N
  234069. 2/28/96V
  234070. Thiiranes and Thiirenes.W
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  234072. GABRIEL WEATHERHEAD
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  234075. Organic Nitrogen Compounds IK
  234076. Georg Thieme VerlagM
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  234080. 1990X
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  234087. Georg Thieme VerlagM
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  234090. Nitroxyl Radicals, NitroxidesW
  234091. 1990X
  234092. 395-403Y
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  234096. Katritzky, A. R.//Rees, C. W.B$Comprehensive Het rocyclic ChemistryC
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  234098. Pergamon PressM
  234099. 19641N
  234100. 2/28/96VEFurans and their Benzo Derivatives: (iii) Synthesis and Applications.W
  234101. 1984X
  234102. GABRIEL WEATHERHEADy
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  234104. 18633
  234105. Dondoni, A.B4Advances in the Use of Synthons in Organic ChemistryK
  234106. Jai Press IncM
  234107. 19642N
  234108. 2/28/96V'New Formyl Anion and Cation EquivalentsW
  234109. 1993X
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  234112. Greenwich, CT
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  234116. Verlag Helvetica Chimica ActaM
  234117. 19643N
  234118. 2/28/96V$Carbohydrate Synt esis via ThiazolesW
  234119. 1992X
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  234121. GABRIEL WEATHERHEADy
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  234123. 18635
  234124. Klamann, D.//Hagemann, H.B1Organic Nitrogen Compounds with a C,N-Double BondM
  234125. 19644
  234126. 2/28/96V9Alkylidenetriazanes, -Triazenes and Higher Aza HomologuesW
  234127. 1990a
  234128. GABRIEL WEATHERHEAD
  234129. 18636
  234130. Klamann, D.//Hagemann, H.B1Organic Nitrogen Compounds with a C,N-Double BondK
  234131. Georg Thieme VerlagM
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  234134. AzinesW
  234135. 1990X
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  234138. GABRIEL WEATHERHEADy    Stuttgart
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  234141. Georg Thieme VerlagM
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  234145. 1990X
  234146. 434-631Y
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  234148. GABRIEL WEATHERHEADy    Stuttgart
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  234150. Trost, B. M.//Fleming, I.B
  234151. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  234153. 19647N
  234154. 2/28/96V!Vinylic and Arylic C-H Oxidation.W
  234155. 1991X
  234156. GABRIEL WEATHERHEADy
  234157. Oxford
  234158. 18639
  234159. Trost, B. M.//Fleming, I.B
  234160. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  234162. 19648N
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  234164. Synthe is of Quinones.W
  234165. 1991X
  234166. GABRIEL WEATHERHEADy
  234167. Oxford
  234168. 18640
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  234170. Rev. Heteroatom Chem.C
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  234172. MYU K.K.M
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  234175. 1988Z
  234176. GABRIEL WEATHERHEADy
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  234183. 2/28/96VhHomolytic Aromatic Hydroxylations via Radiolysis of Aqueous Solutions and via Metal Ion-Oxygen  Systems.W
  234184. 19 1Z
  234185. GABRIEL WEATHERHEADy
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  234187. 18642
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  234189. Heteroarenes I, Part 1K
  234190. Georg Thieme VerlagM
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  234193. FuransW
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  234196. GABRIEL WEATHERHEADy    Stuttgart
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  234200. Georg Thieme VerlagM
  234201. 19652N
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  234203. 1H-ImidazolesW
  234204. 1994X
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  234209. Jai Press, Inc.M
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  234211. 2/28/96V@Carbon-Centered Radicals from Amino Acids and their Derivatives.W
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  234213. GABRIEL WEATHERHEAD
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  234217. Heteroarenes III, Part 1K
  234218. Georg Thieme VerlagM
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  234220. 2/28/96V*1,2-Dithiolium Salts and Related CompoundsW
  234221. 1993X
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  234229. 2/28/96V#Cyclobutene Ring Opening Reactions.W
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  234233. 18647
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  234239. 2/28/96V1Other Fused-ring Azetidines, Azetines and Azetes.
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  234241. GABRIEL WEATHERHEADy
  234242. Oxford
  234243. 18648
  234244. Trost, B. M.//Fleming, I.B
  234245. Comprehensive Organic SynthesisC2FUNCTIONAL GROUPS /REDUCTION /Al /HYDROMETALLATIONK
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  234247. 19657N
  234248. 2/28/96V$Hydroalumination of C=C and Alkynes.W
  234249. 1991X
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  234251. Oxford
  234252. 18649
  234253. NA    Kropf, H.B
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  234255.  Georg Thieme VerlagM
  234256. 19658N
  234257. 2/28/96V5Derivatives of Monoperoxy and Diperoxy Carbonic AcidsW
  234258. 1988X
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  234260. GABRIEL WEATHERHEADy    Stuttgart
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  234264. Georg Thieme VerlagM
  234265. 19659N
  234266. 2/28/96V&Derivatives of Peroxy Dicarbonic AcidsW
  234267. 1988X
  234268. 917-931Y
  234269. GABRIEL WEATHERHEADy    Stuttgart
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  234272. Modern Synthetic Methods.K
  234273. Otto Salle VerlaM
  234274. 19660N
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  234285. 1984X
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  234288. Oxford
  234289. 18653
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  234291. DIOXOLANES /OXATHIOLANESK
  234292. Pergamon PressM
  234293. 19662N
  234294. 2/28/96V
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  234296. 1984X
  234297. GABRIEL WEATHERHEADy
  234298. Oxford
  234299. 18654
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  234301. INDAZOLES /ISOINDAZOLES /PYRAZOLENINES /ISOPYRAZOLES /PYRAZOLINES /INDAZOLONES  /PYRAZOLIDINEDIONES /PYRAZOLIDINES /PYRAZOLIDINONES /PYRAZOLINONES /PYRAZOLONES  /INDAZOLINESK
  234302. Pergamon PressM
  234303. 19663N
  234304. 2/28/96V&Pyrazoles and their Benzo Derivatives.W
  234305. 1984X
  234306. GABRIEL WEATHERHEADy
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  234308. 18655
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  234310. Heteroarenes I, Part 2K
  234311. Georg Thieme VerlagM
  234312. 19664N
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  234315. 1994X
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  234317. GABRIEL WEATHERHEADy    Stuttgart
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  234321. Georg Thieme VerlagM
  234322. 19665N
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  234325. 1990X    1052-1136Y
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  234330. Organic Nitrogen Compounds IK
  234331. Georg Thieme VerlagM
  234332. 19666N
  234333. 2/28/96V
  234334. Organotr azenesW
  234335. 1990X    1182-1226Y
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  234339. Morrison, J. D.B>Asymmetric Synthesis. Stereodifferentiating Reactions, Part B.C
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  234342. 2/28/96V Alkylation of Chiral Hydrazones.W
  234343. 1984X
  234344. GABRIEL WEATHERHEADy
  234345. New York
  234346. 18659
  234347. Regitz, M.B
  234348. Organophosphorus Compounds IK
  234349. Georg Thieme VerlagM
  234350. 19668N
  234351. 2/28/96V@Phosphorus(III) Compounds with Coordination Number 3: PhosphanesW
  234352. 1982X
  234353. 106-182Y
  234354. GABRIEL WEATHERHEADy    Stuttgart
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  234356. Mayo, P. D.
  234357. YB,Rearrangements in Ground and Excited States.C PHYSICAL ORGANIC /REARRANGEMENTSK
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  234359. 2/28/96V'Rearrangements: A Theoretical Approach.W
  234360. 1980X
  234361. GABRIEL WEATHERHEADy
  234362. New York
  234363. 18661
  234364. Trost, B. M.//Fleming, I.B
  234365. Comprehensive Organic SynthesisC5FUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENATIONK
  234366. Pergamon PressM
  234367. 19670N
  234368. 2/28/96VAHydrogenolysis of Allyl and Benzyl Halides and Related Compounds.W
  234369. 1991X
  234370. GABRIEL WEATHERHEADy
  234371. Oxford
  234372. 18662
  234373. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.K
  234374. Academic PressM
  234375. 19671N
  234376. 2/28/96V(The Total Synthesis of Retigeranic Acid.W
  234377. 1988Z
  234378. GABRIEL WEATHERHEAD
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  234380. Janoschek, R.B1Chirality : from Weak Bosons to the Alpha - HelixK
  234381. SpringerM
  234382. 19672N
  234383. 2/28/96V8Chirality in Organic Synthesis - The Use of BiocatalystsW
  234384. 1991X
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  234386. GABRIEL WEATHERHEADy
  234387. Berlin
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  234392. Pergamon PressM
  234393. 19673N
  234394. 2/28/96V&The Aliphatic Friedel-Crafts Reaction.W
  234395. 1991X
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  234398. 18665
  234399. Morr son, J. D.B>Asymmetric Synthesis. Stereodifferentiating Reactions, Part B.CmC-C BOND FORMATION /APPENDAGES /ENOLATES /ALKYLATION /ENANTIOGENIC REACTIONS  /C=C-X-M /O-L /ENANTIOSELECTIVEK
  234400. 19674N
  234401. 2/28/96V>Stereoselective Alkylation Reactions of Chiral Metal Enolates.W
  234402. 1984X
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  234407. Comprehensive Organic SynthesisC,ORGANOMETALLICS /TITANIUM /ZIRCONIUM /Ti /ZrK
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  234409. 19675N
  234410. 2/28/96V,Organotitanium and Organozirconium Reagents.W
  234411. 1991X
  234412. GABRIEL WEATHERHEADy
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  234414. 18667
  234415. Klamann, D.B
  234416. Organosulfur CompoundsK
  234417. Georg Thieme VerlagM
  234418. 19676N
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  234422. GABRIEL WEATHERHEADy    Stuttgart
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  234425. 19677N
  234426. 2/28/96V1The Design of a Chemoselective Reduction CatalystW
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  234428. GABRIEL WEATHERHEAD
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  234430. Curra , D. P.B Advances in Cycloaddition, Vol 3K
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  234435. 1993X
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  234437. GABRIEL WEATHERHEADy
  234438. Greenwich, CT
  234439. 18670
  234440. Hagemann, H.B
  234441. Carbonic Acid DerivativesK
  234442. Georg Thieme VerlagM
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  234451. Kluwer Academic PublM
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  234454. dVpMechanisms in Stereo-Differentiating Metal-Catalyzed Reactions - Enantioselective Palladium-C talyzed AllylationW
  234455. 1991X
  234456. 107-131a
  234457. GABRIEL WEATHERHEADy
  234458. Dordrecht, Netherlands
  234459. 18672
  234460. Trost, B. M.//Fleming, I.B
  234461. Comprehensive Organic SynthesisC.ORGANOMETALLICS /SILICON /TIN /C=C-C-M /Si /SnK
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  234464. 2/28/96V1Allylsilanes, Allylstannanes and Related Systems.W
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  234466. GABRIEL WEATHERHEADy
  234467. Oxford
  234468. 18673
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  234470. Organophosphorus Compounds IIK
  234471. Georg Thieme VerlagM
  234472. 19682N
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  234474. 1982X
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  234478. Giuliano, R. M.B1Cycloaddition Reactions in Carbohydrate ChemistryK
  234479. Amer Chemical SocM
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  234481. 2/28/96V\Stereoselectivity of 1,3-Dipolar Cycloaddition of Glycosyl Nitrones to Normal-ArylmaleimidesW
  234482. 1992X
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  234484. GABRIEL WEATHERHEADy
  234485. Washington, DC
  234486. 18675
  234487. Scheffold, R.
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  234489. Otto Salle VerlagM
  234490. 19684N
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  234494. GABRIEL WEATHERHEADy
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  234502. GABRIEL WEATHERHEADy
  234503. Oxford
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  234507. GABRIEL WEATHERHEAD
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  234509. Bartl, H.//Falbe, J.B
  234510. Macromolecular MaterialsK
  234511. Georg Thieme VerlagM
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  234513. 2/28/96V"Optically Active (Chiral) PolymersW
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  234519. Georg Thieme VerlagM
  234520. 19688N
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  234522. Liquid Crystalline Po ymersW
  234523. 1987X    2201-2207Y
  234524. GABRIEL WEATHERHEADy    Stuttgart
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  234529. 2/28/96V'A Unified View of Ketone PhotochemistryW
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  234535. Georg Thieme VerlagM
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  234537. 2/28/96V2(3.3.3)Cyclazines (Pyrido[2,1,6-d /e]quinolizines)W
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  234547. GABRIEL WEATHERHEADy
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  234551. Arenes and ArinesK
  234552. Georg Thieme VerlagM
  234553. 19692N
  234554. 2/28/96VLPreparation: By Construction of Aromatic Systems from Non-Aromatic CompoundsW
  234555. 1981X
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  234558. GABRIEL WEATHERHEADy    Stuttgart
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  234560. qB&Silicon Compounds, Register and ReviewC
  234561. Petrarch SystemsM
  234562. 19693N
  234563. 2/28/96V7Silicon-mediated stereochemically controlled reactions.W
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  234571. 2/28/96V>Carbocycles from Carbohydrates: The Annulated Sugar 'Approach'W
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  234579. 1,2,4-Thiadiazoles.W
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  234581. GABRIEL WEATHERHEADy
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  234584. Giuliano, R. M.B1Cycloaddition Reactions in Carbohydrate ChemistryC
  234585. DIELS-ALDER REACTION/DIASTEREOFACIAL REACTIVITY/ALLYLIC  SUBSTITUENTS/CYCLO-ADDITION/CYCLOPENTADIENE/SELECTIVITY/DERIVATIVES/AUXILIARIES/DIENES/MODELK
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  234588. 2/28/96V0Carbohydrate Dienophiles in <4+2> CycloadditionsW
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  234597. 2/28/96VrPalladium Catalyzed Reduction of Aryl Sulfonates - Selectivity Control and Application to  Anthracycline ChemistryW
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  234606. 2/28/96VHPyridines and their Benzo Derivatives: (iv) Reactivity of Non-aromatics.W
  234607. 1984X
  234608. GABRIEL WEATHERHEADy
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  234610. 18690
  234611. wA-Volman, D. H.//Hammond, G. S.//Neckers, D. C.B
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  234613. John Wiley & Son  IncM
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  234615. 2/28/96V4Primary Photoprocesses in Transition Metal ComplexesW
  234616. 1991X
  234617. 215-248Z
  234618. GABRIEL WEATHERHEADy
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  234621. Suschitzky, H.//Scriven, E. F.B#Progress in Heterocyclic Chemistry,C
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  234624. 2/28/96V!Naturally occurring 1,2-dithiins.
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  234626. GABRIEL WEATHERHEADy
  234627. Oxford, U.K.
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  234629. Kropf, H.//Schaumann, E.B
  234630. Ene,X and Yne,X-CompoundsK
  234631. Georg Thieme VerlagM
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  234634. Ene-O-CompoundsW
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  234646. 1993X    1468-1598Y
  234647. GABRIEL WEATHERHEADy    Stuttgart
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  234651. Georg Thieme VerlagM
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  234654. SemioxocarbonsW
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  234656. GABRIEL WEATHERHEADy    Stuttgart
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  234661. 2/28/96VvAutomated Synthesis, Structure and Biological Activity of Backbone-Modified Oligonucleotides -  The Antisense ApproachW
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  234672. 2/28/96VWReduction of alpha-Substituted Carbonyl Compounds -CX-CO to Carbonyl Compounds -CH-CO-.W
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  234674. GABRIEL WEATHERHEADy
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  234676. 18697
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  234678. BiocatalysisC2CARBOHYDRATES /CHIRAL SYNTHON /ASYM /CARBOHYDRATESK
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  234681. 2/28/96V\Simple Carbohydrates as Starting Materials in Organic Synthesis: a Comparison of Strategies.W
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  234715. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.C*7-OXA /PGF2a /13 /14-DEHYDROPROSTAGLANDINSK
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  234721. GABRIEL WEATHERHEAD
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  234739. GABRIEL WEATHERHEADy    Greenwich
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  234781. 2/28/96V,Synthetic Studies on Pentacyclic QuassinoidsW
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  234784. GABRIEL WEATHERHEADy
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  234794. GABRIEL WEATHERHEADy    Stuttgart
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  234798. Georg Thieme VerlagM
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  234800. 2/28/96VQPhosphorus(V) Compounds with Coordination / Number 4: Phosphoric Acid DerivativesW
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  234803. GABRIEL WEATHERHEADy    Stuttgart
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  234807. Georg Thieme VerlagM
  234808. 19720N
  234809. 2/28/96V-Acyl (alpha-Heterosubstituted)alkyl PeroxidesW
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  234812. GABRIEL WEATHERHEADy    Stuttgart
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  234814. German, L.//Z mskov, S.
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  234816. SpringerM
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  234818. 2/28/96VXHigher fluorides of group V and VI elements as fluorinating agents in organic synthesis.W
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  234820. GABRIEL WEATHERHEADy
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  234822. 18713
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  234824. SpringerM
  234825. 19722N
  234826. 2/28/96V(Some 'elecrophilic' fluorination agents.W
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  234833. 2/28/96VTMechanisms and Catalysis in Electron Transfer Chemistry of Redox Coenzyme Analogues.W
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  234835. GABRIEL WEATHERHEAD
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  234841. 2/28/96V
  234842. Nitrogen Stabilization.W
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  234844. GABRIEL WEATHERHEADy
  234845. Oxford
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  234847. Trost, B. M.//Fleming, I.B
  234848. Comprehensive Organic SynthesisC3C-C BOND FORMATION /APPENDAGES /ALKYLATION /ALKYNESK
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  234851. 2/28/96
  234852. V"Alkylations of Alkynyl Carbanions.W
  234853. 1991X
  234854. GABRIEL WEATHERHEADy
  234855. Oxford
  234856. 18717
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  234858. C-RadicalsK
  234859. Georg Thieme VerlagM
  234860. 19726N
  234861. 2/28/96V3Reactions of Radicals with Formation of a  C,C-BondW
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  234865. GABRIEL WEATHERHEADy    Stuttgart
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  234869. Georg Thieme VerlagM
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  234871. 2/28/96V&2-Benzothiophenes (Benzo[c]thiophenes)W
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  234874. GABRIEL WEATHERHEADy    Stuttgart
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  234877. Comprehensive Organic SynthesisC6C-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITIONK
  234878. Pergamon PressM
  234879. 19728N
  234880. 2/28/96V&Asymmetric Synthesis with Enol Ethers.W
  234881. 1991X
  234882. GABRIEL WEATHERHEADy
  234883. Oxford
  234884. 18720
  234885. Trost, B. M.//Fleming, I.B
  234886. Comprehensive Organic SynthesisC4C-C BOND FORMATION /APPENDAG S /ENOLATES /ALKYLATIONK
  234887. Pergamon PressM
  234888. 19729N
  234889. 2/28/96V.Alkylations of Nitrogen-stabilized Carbanions.W
  234890. 1991X
  234891. GABRIEL WEATHERHEAD
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  234894. Hudlicky, T.B#Organic Synthesis: Theory and Appl.C1ODDS AND ENDS /TECHNIQUES AND METHODS /SONICATIONK
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  234897. 2/28/96VlNonconventional Reaction Conditions: Ultrasound, High Pressure, and Microwave Heating in Organic  Synthesis.W
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  234904. Georg Thieme VerlagM
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  234906. 2/28/96W&1989  C-Radicals: General IntroductionX
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  234912. Comprehensive Organic SynthesisCZC-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[2+2] /HETEROANNULATION  /4-RINGK
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  234915. 2/28/96W.1991  Formation of Four-membered Heterocycles.X
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  234919. Trost, B. M.//Fleming, I.B
  234920. Comprehensive Organic SynthesisC.PHYSICAL ORGANIC /REARRANGEMENTS /HOMOLOGATIONK
  234921. Pergamon PressM
  234922. 19733N
  234923. 2/28/96V
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  234925. GABRIEL WEATHERHEADy
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  234928. Trost, B. M.//Fleming, I.B
  234929. Comprehensive Organic SynthesisC PHYSICAL ORGAN C /REARRANGEMENTSK
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  234931. 19734N
  234932. 2/28/96V$Benzil-Benzilic Acid Rearrangements.W
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  234934. GABRIEL WEATHERHEADy
  234935. Oxford
  234936. 18726
  234937. Trost, B. M.//Fleming, I.B
  234938. Comprehensive Organic SynthesisC.FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUS /PK
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  234940. 19735N
  234941. 2/28/96V% xidation of Nitrogen and Phosphorus.W
  234942. 1991X
  234943. GABRIEL WEATHERHEADy
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  234945. 18727
  234946. Trost, B. M.//Fleming, I.B
  234947. Comprehensive Organic SynthesisC
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  234950. 19736N
  234951. 2/28/96V)Reduction of N=N, N-N, N-O and O-O Bonds.W
  234952. 1991X
  234953. GABRIEL WEATHERHEADy
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  234964. Klamann, D.//Hagemann, H.B1Organic Nitrogen Compounds with a C,N-Dou le BondK
  234965. Georg Thieme VerlagM
  234966. 19738N
  234967. 2/28/96V
  234968. Hydrazonium SaltsW
  234969. 1990X
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  234976. Georg Thieme VerlagM
  234977. 19739N
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  234980. 1990X    1035-1051Y
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  234982. GABRIEL WEATHERHEADy    Stuttgart
  234983. 18731
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  234986. Georg Thieme VerlagM
  234987. 19740N
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  234990.  1990X
  234991. 997-1034Y
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  234993. GABRIEL WEATHERHEADy    Stuttgart
  234994. 18732
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  234998. 19741N
  234999. 2/28/96V(Nucleophiles with Allyl-Metal Complexes.W
  235000. 1991X
  235001. GABRIEL WEATHERHEADy
  235002. Oxford
  235003. 18733
  235004. Trost, B. M.//Fleming, I.B
  235005. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  235007. 19742N
  235008. 2/28/96V'Oxidation Adjacent to Oxygen of Ethers.W
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  235010. GABRIEL WEATHERHEADy
  235011. Oxford
  235012. 18734
  235013. Giuliano, R. M.B1Cycloaddition Reactions in Carbohydrate ChemistryC
  235014. DIELS-ALDER REACTIONS/RESEMBLE GRANDFATHER GLUCOSE/DIACETONE GLUCOSE/ASYMMETRIC  DIELS/2,3-UNSATURATED SUGARS/CHIRAL  AUXILIARIES/CYCLO-ADDITION/DIENES/ROUTE/CYCLOPENTADIENEK
  235015. Amer Chemical SocM
  235016. 19743N
  235017. 2/28/96V?Cycloaddition Reactions in Carbohydrate Chemistry - An OverviewW
  235018. 1992X
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  235020. GABRIEL WEATHERHEADy
  235021. Washington, DC
  235022. 18735
  235023. Oae, S.B
  235024. Rev. Heteroatom Chem.K
  235025. MYU K.K.M
  235026. 19744N
  235027. 2/28/96Vgalpha-Aminocarbonyl and related compounds in the syntheses of the derivatives of  1,3,2-oxazaphosphole.W
  235028. 1992a
  235029. GABRIEL WEATHERHEADy
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  235031. 18736
  235032. Apsimon, J.B*Total Synthesis of Natural Products, Vol 8K
  235033. John Wiley & Sons IncM
  235034. 19745N
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  235036. V;The Total Synthesis of Tricyclic and Tetracyclic DiterpenesW
  235037. 1992X
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  235039. GABRIEL WEATHERHEADy
  235040. New York, NY
  235041. 18737
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  235043. Heteroarenes III, Part 4K
  235044. Georg Thieme VerlagM
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  235047. 1,2,3,4-OxatriazolesW
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  235050. GABRIEL WEATHERHEADy    Stuttgart
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  235057. DithiadiazolesW
  235058. 1994X
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  235060. GABRIEL WEATHERHEADy    Stuttgart
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  235088. GABRIEL WEATHERHEAD
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  235094. 2/28/96VBReductions with Chiral Modifications of Lithium Aluminium Hydride.W
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  235100. Pergamon PressM
  235101. 19752N
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  235110. Georg Thieme VerlagM
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  235125. 18746
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  235130. 19755N
  235131. 2/28/96VXPartial and Complete Reductions of Pyrroles, Furans, Thiophenes and their Benzo Analogs.W
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  235141. GABRIEL WEATHERHEADy
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  235143. 18748
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  235147. 19757N
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  235174. 19760N
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  235176. 1984X
  235177. GABRIEL WEATHERHEADy
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  235179. 18752
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  235187. 18753
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  235221. GABRIEL WEATHERHEADy
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  235234. 19767N
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  235236. Nitrilium SaltsW
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  235238. GABRIEL WEATHERHEADy    Stuttgart
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  235242. Georg Thieme VerlagM
  235243. 19768N
  235244. 2/28/96VKPreparation: From Aromatic Compounds by Substitution with Functional GroupsW
  235245. 1981X
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  235263. Georg Thieme VerlagM
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  235267. 1981X
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  235270. GABRIEL WEATHERHEADy    Stuttgart
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  235274. Georg Thieme VerlagM
  235275. 19771N
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  235277. P eparation of Labelled ArenesW
  235278. 1981X
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  235281. GABRIEL WEATHERHEADy    Stuttgart
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  235285. Georg Thieme VerlagM
  235286. 19772N
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  235288. 1981X
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  235291. GABRIEL WEATHERHEADy    Stuttgart
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  235295. Georg Thieme VerlagM
  235296. 19773N
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  235298. Ar nes and Arines: IntroductionW
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  235302. GABRIEL WEATHERHEADy    Stuttgart
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  235321. GABRIEL WEATHERHEADy
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  235326. 19776N
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  235329. GABRIEL WEATHERHEADy
  235330. Oxford
  235331. 18768
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  235333. Organosulfur CompoundsK
  235334. Georg Thieme VerlagM
  235335. 19777N
  235336. 2/28/96V&Protecting Groups for Sulfur CompoundsW
  235337. 1985X    1622-1638Y
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  235341. Georg Thieme VerlagM
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  235345. 1985X    1591-1610Y
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  235353. 1985X    1611-1658Y
  235354. GABRIEL WEATHERHEADy    Stuttgart
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  235402. Georg Thieme VerlagM
  235403. 19785N
  235404. 2/28/96V*Heterotriorgano- and TetraorganosulfuranesW
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  235407. GABRIEL WEATHERHEADy    Stuttgart
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  235411. Georg Thieme VerlagM
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  235417. GABRIEL WEATHERHEADy    Stuttgart
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  235421. Georg Thieme VerlagM
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  235427. GABRIEL WEATHERHEADy    Stuttgart
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  235444. 1987X    1994-2182Y
  235445. GABRIEL WEATHERHEADy    Stuttgart
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  235449. Georg Thieme VerlagM
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  235451. 2/28/96VNReduction with Inorganic Reducing Agents:  Metal Hydrides and Complex HydridesW
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  235458. Carbonic Acid DerivativesK
  235459. Georg Thieme VerlagM
  235460. 19791N
  235461. 2/28/96VXDicarbonic Acid Derivatives with an Isocyanate, Isothiocyanate and Carbodiimide FunctionW
  235462. 1983X    1234-1274Y
  235463. GABRIEL WEATHERHEADy    Stut gart
  235464. 18783
  235465. Hagemann, H.B
  235466. Carbonic Acid DerivativesK
  235467. Georg Thieme VerlagM
  235468. 19792N
  235469. 2/28/96V3Monocarbonic Acid Derivatives with a Cyano FunctionW
  235470. 1983X
  235471. 915-999Y
  235472. GABRIEL WEATHERHEAD
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  235474. 18784
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  235477. Georg Thieme VerlagM
  235478. 19793N
  235479. 2/28/96V\Monocarbonic Acid Derivatives: Simple Monocarbonic Acid Derivatives with a Carbonyl FunctionW
  235480. 1983X
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  235482. GABRIEL WEATHERHEADy    Stuttgart
  235483. 18785
  235484. A    Falbe, J.B7Organo-pi-metal Compounds as Acids in Organic ChemistryK
  235485. Georg Thieme VerlagM
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  235487. 2/28/96V Catalytic Reactions: EliminationW
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  235497. Georg Thieme VerlagM
  235498. 19796N
  235499. 2/28/96V
  235500. Vinyl and Aryl CationsW
  235501. 1990X
  235502. 97-250Y
  235503. E19ca
  235504. GABRIEL WEATHERHEADy    Stuttgart
  235505. 18788
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  235507. Georg Thieme VerlagM
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  235510. Alkynyl CationsW
  235511. 1990X
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  235520. 2/28/96V+Synthetic Studies on Molecular Recognition.W
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  235522. GABRIEL WEATHERHEADy
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  235528. 2/28/96V
  235529. Crown Ethers and Cryptands.W
  235530. 1984X
  235531. GABRIEL WEATHERHEADy
  235532. Oxford
  235533. 18791
  235534. Pearson, H. W.B#Adv. Heterocyclic Nat. Prod. Synth.C
  235535. S /SeK    Jai PressM
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  235537. 2/28/96VpEpisulfonium Ions and Episelenonium Ions. Versatile Heterocyclic Cations for the Synthesis of  Natural Products.W
  235538. 1992X
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  235540. GABRIEL WEATHERHEADy
  235541. Greenwich, CT
  235542. 18792
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  235545. Pergamon PressM
  235546. 19801N
  235547. 2/28/96V&Electrophilic Heteroatom Cyclizations.W
  235548. 1991X
  235549. GABRIEL WEATHERHEADy
  235550. Oxford
  235551. 18793
  235552. Trost, B. M.//Fleming, I.B
  235553. Comprehensive Organic SynthesisC5FUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENA IONK
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  235559. GABRIEL WEATHERHEADy
  235560. Oxford
  235561. 18794
  235562. Morrison, J. D.B
  235563. Asymmetric Synthesis.C
  235564. FUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENATION /ENANTIOGENIC REACTIONS  /STEREOCHEMISTRY /ASYMMETRIC HETEROGENEOUS /O=C(R)-C-X /OH,NK
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  235566. 2/28/96V1Asymmetric Heterogeneous  atalytic Hydrogenation.W
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  235575. 2/28/96V
  235576. Wagner-Meerwein Rearrangements.W
  235577. 1991X
  235578. GABRIEL WEATHERHEADy
  235579. Oxford
  235580. 18796
  235581. Schaumann, E.B
  235582. Heteroarenes III, Part 1K
  235583.  Georg Thieme VerlagM
  235584. 19805N
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  235586. 1,3-Dioxolium SaltsW
  235587. 1993X
  235588. GABRIEL WEATHERHEADy    Stuttgart
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  235590. Schaumann, E.B
  235591. Heteroarenes III, Part 1K
  235592. Georg Thieme VerlagM
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  235594. 2/28/96V
  235595. 1,3-Oxathiolium SaltsW
  235596. 1993X
  235597. 10-44Y
  235598. GABRIEL WEATHERHEAD
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  235600. 18798
  235601. Hartley, F. R.B8The Use of Organometallic Compound Organic in Synthesis.K
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  235604. 2/28/96V"Supported Metal Complex Catalysts.W
  235605. 1987X    1163-1225Z
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  235611. 19808N
  235612. 2/28/96V7Fused-ring Oxiranes, Oxirenes, Thiiranes and Thiirenes.W
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  235614. GABRIEL WEATHERHEADy
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  235616. 18800
  235617. Trost, B. M.//Fleming, I.B
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  235619. Pergamon PressM
  235620. 19809N
  235621. 2/28/96V(Transannular Electrophilic Cyclizations.W
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  235623. GABRIEL WEATHERHEADy
  235624. Oxford
  235625. 18801
  235626. Fleming, I.B-Comprehensive Organic Synthesis  Trost, B. M.K
  235627. Pergamon PressM
  235628. 19810N
  235629. 2/28/96V8The Benzoin and Related Acyl Anion Equivalent Reactions.W
  235630. 1991X
  235631. GABRIEL WEATHERHEAD
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  235633. 18802
  235634. Klamann, D.B
  235635. Organic Nitrogen Compounds IK
  235636. Georg Thieme VerlagM
  235637. 19811N
  235638. 2/28/96V
  235639. C-Azido CompoundsW
  235640. 1990X    1243-1290Y
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  235645. CarbohydratesK
  235646. Kodansha LtdM
  235647. 19812N
  235648. 2/28/96VuSystematic Synthesis of Gangliosides Toward the Elucidation and Biomedical Application of Their  Biological FunctionsW
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  235656. Georg Thieme VerlagM
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  235666. Oxidation Part IK
  235667. Georg Thieme VerlagM
  235668. 19814N
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  235671. 1981X
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  235678. Georg Thieme VerlagM
  235679. 19815N
  235680. 2/28/96V
  235681. 1,2,4-Dithiazolium SaltsW
  235682. 1994X
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  235684. GABRIEL WEATHERHEADy    Stuttgart
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  235686. Trost, B. M.//Fleming, I.B
  235687. Comprehensive Organic SynthesisC2FUNCTIONAL GROUPS /TRANSFORMATIONS /O=C-X TO O=C-YK
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  235689. 19816N
  235690. 2/28/96V4The Intramolecular Aromatic Friedel-Crafts Reaction.W
  235691. 1991X
  235692. GABRIEL WEATHERHEADy
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  235694. 18808
  235695. Morrison, J. D.B
  235696. Asymmetric Synthesis.CyC-C BOND FORMATION /APPENDAGES /COUPLING /ENANTIOGENIC REACTIONS /MAGNESIUM /STEREOCHEMISTRY /C-M /Mg /KINETIC RESOLUTIONK
  235697. 19817N
  235698. 2/28/96V
  235699. Asymmetric Coupling Reactions.W
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  235701. GABRIEL WEATHERHEADy
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  235703. 18809
  235704. Trost, B. M.//Fleming, I.B
  235705. Comprehensive Organic SynthesisC.FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUSK
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  235707. 19818N
  235708. 2/28/96V
  235709. Inorganic Acid Derivatives.W
  235710. 1991X
  235711. GABRIEL WEATHERHEADy
  235712. Oxford
  235713. 18810
  235714. Trost, B. M.//Fleming, I.B
  235715. Comprehensive Organic SynthesisC
  235716. ORGANOMETALLICS /ALUMINIUM /AlK
  235717. Pergamon PressM
  235718. 19819N
  235719. 2/28/96V
  235720. Organoaluminium Reagents.W
  235721. 1991X
  235722. GABRIEL WEATHERHEAD
  235723. Oxford
  235724. 18811
  235725. Trost, B. M.//Fleming, I.B
  235726. Comprehensive Organic SynthesisC
  235727. ORGANO ETALLICS /PALLADIUM /PdK
  235728. Pergamon PressM
  235729. 19820N
  235730. 2/28/96V7Vinyl Substitutions with Organopalladium Intermediates.W
  235731. 1991X
  235732. GABRIEL WEATHERHEADy
  235733. Oxford
  235734. 18812
  235735. Scheffold, R.B
  235736. Mo ern Synthetic MethodsK
  235737. Verlag Helvetica Chimica ActaM
  235738. 19821N
  235739. 2/28/96V
  235740. Modern Enolate Chemistry: Regio- and Stereoselective Formation of Enolates       and the  Consequence of Enolate Configuration on Subsequent ReactionsW
  235741. 1992X
  235742. 1-102Z
  235743. GABRIEL WEATHERHEADy
  235744. Basel, Switzerland
  235745. 18813
  235746. Trost, B. M.//Fleming, I.B
  235747. Comprehensive Organic SynthesisC6C-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITIONK
  235748. Pergamon PressM
  235749. 19822N
  235750. 2/28/96V2The Aldol Reaction: Group I and Group II Enolates.W
  235751. 1991X
  235752. GABRIEL WEATHERHEADy
  235753. Oxford
  235754. 18814
  235755. Trost, B. M.//Fleming, I.B
  235756. Comprehensive Organic SynthesisC6C-C BOND FOR ATION /APPENDAGES /ENOLATES /1,2-ADDITION
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  235758. 19823N
  235759. 2/28/96V4The Aldol Reaction: Acid and General Base Catalysis.W
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  235761. GABRIEL WEATHERHEADy
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  235763. 18815
  235764. Morrison, J. D.B>Asymmetric Synthesis. Stereodifferentiating Reactions  Part B.C
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  235773. Trost, B. M.//Fleming, I.B
  235774. Comprehensive Organic SynthesisCbFUNCTIONAL GROUPS /TRANSFO MATIONS /O=C-X TO O=C-Y /C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGEK
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  235776. 19825N
  235777. 2/28/96V1The Bimolecular Aromatic Friedel-Crafts Reaction.W
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  235779. GABRIEL WEATHERHEADy
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  235782. Trost, B. M.//Fleming, I.B
  235783. Comprehensive Organic SynthesisC.C-C BOND FORMATION /AROMATICS /CHAIN EXTENSION
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  235785. 19826N
  235786. 2/28/96V*The Bimolecular Aromatic Mannich Reaction.W
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  235788. GABRIEL WEATHERHEADy
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  235790. 18818
  235791. A    Falbe, J.B    AldehydesK
  235792. Georg Thieme VerlagM
  235793. 19827N
  235794. 2/28/96VNPreparation of Aldehydes by Rearrangement with Conservation of Carbon SkeletonW
  235795. 1983X
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  235797. GABRIEL WEATHERHEADy    Stuttgart
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  235799. Kropf, H.//Schaumann, E.B
  235800. Ene,X and Yne,X-CompoundsK
  235801. Georg Thieme VerlagM
  235802. 19828N
  235803. 2/28/96V
  235804.  etraheterosubstituted EthenesW
  235805. 1993X    2882-2932Y
  235806. GABRIEL WEATHERHEADy    Stuttgart
  235807. 18820
  235808. Kropf, H.//Schaumann, E.B
  235809. Ene,X and Yne,X-CompoundsK
  235810. Georg Thieme VerlagM
  235811. 19829N
  235812. 2/28/96V1Monoheterofunctionally Substituted Ketene AcetalsW
  235813. 1993X    2710-2817Y
  235814. GABRIEL WEATHERHEADy    Stuttgart
  235815. 18821
  235816. Schlosser, M.B
  235817. Organo etallics. A ManualC
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  235820. 2/28/96V
  235821. Palladium in Organic SynthesisW
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  235827. Trost, B. M.//Fleming, I.
  235828. Comprehensive Organic SynthesisC>C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /CARBOMETALLATIONK
  235829. Pergamon PressM
  235830. 19831N
  235831. 2/28/96V-Carbon Nucleophiles with Alkenes and Alkynes.W
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  235833. GABRIEL WEATHERHEADy
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  235835. 18823
  235836. Trost, B. M.//Fleming, I.B
  235837. C mprehensive Organic SynthesisC5C-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATIONK
  235838. Pergamon PressM
  235839. 19832N
  235840. 2/28/96VAHeteroatom Nucleophiles with Metal-activated Alkenes and Alkynes.W
  235841. 1991X
  235842. GABRIEL WEATHERHEADy
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  235844. 18824
  235845. Scheffold, R.B
  235846. Modern Synthetic Methods.CHORGANOMETALLICS /SYNTHESIS /NICKEL /PALLADIUM /IRON /C-M /Ni /Pd /Fe /TMK
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  235849. 2/28/96V2Group VIII Transition Metals in Organic Synthesis.W
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  235856. Georg Thieme VerlagM
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  235860. 1988X
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  235862. GABRIEL WEATHERHEADy    Stuttgart
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  235866. Georg Thieme VerlagM
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  235869. Peroxy Iminocarboxylic AcidsW
  235870. 1988X
  235871. 898-899Y
  235872. GABRIEL WEATHERHEADy    Stuttgart
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  235875. Organic Nitrogen Compounds IVK
  235876. Georg Thieme VerlagM
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  235878. 2/28/96V
  235879. AminesW
  235880. 1992X
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  235885. A    Falbe, J.B7Organo-pi-metal Compounds as Acids in Organic ChemistryK
  235886. Georg Thieme VerlagM
  235887. 19837N
  235888. 2/28/96V
  235889. Catalytic  eactions: C-C Bond Formation Reactions (Hydrocarbonation, Carbometallation, Carbene Addition  Reactions, Insertion Reactions)W
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  235892. GABRIEL WEATHERHEADy    Stuttgart
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  235895. Georg Thieme VerlagM
  235896. 19838N
  235897. 2/28/96VFCatalytic Reactions: Hydrogenation, Hydrometallation and DimetallationW
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  235900. GABRIEL WEATHERHEADy    Stuttgart
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  235903. Georg Thieme Verlag
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  235905. 2/28/96VKCatalytic Reactions: Carbohalogenation, Carbooxygenation and CarboaminationW
  235906. 1986X    1041-1044Y
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  235909. Trost, B. M.//Fleming, I.B
  235910. Comprehensive Organic SynthesisC&C-C BOND FORMATION /ANNULATION /3-RINGK
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  235912. 19840N
  235913. 2/28/96VJMethylene and Nonfunctionalized Alkylidene Transfer to Form Cyclopropanes.W
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  235915. GABRIEL WEATHERHEADy
  235916. Oxford
  235917. 18832
  235918. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.K
  235919. Academic PressM
  235920. 19841N
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  235922. -Valerolactone Annulation: Application to the Total Synthesis of Quadrone.W
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  235924. GABRIEL WEATHERHEAD
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  235926. Liebeskind, L. S.B
  235927. Adv. Metal-Organic Chem.C
  235928. ORGANOMETALLICS /IRON /FeK
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  235940. 19843N
  235941. 2/28/96VDAsymmetric Diels-Alder Reactions with Chiral Enoates as Dienophiles.W
  235942. 1986X
  235943. GABRIEL WEATHERHEADy
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  235946. A)Noels, A. F.//Graziani, M.//Hubert, A. J.B/Metal Promoted Selectivity in Organic SynthesisK
  235947. Kluwer Academic PublM
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  235950. 1991X
  235951. 133-159a
  235952. GABRIEL WEATHERHEADy
  235953. Dordrecht, Netherlands
  235954. 18836
  235955. Schaumann, E.B
  235956. Heteroarenes III, Part 3K
  235957. Georg Thieme VerlagM
  235958. 19845N
  235959. 2/28/96V
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  235961. 1994X
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  235974. Kreher, R. P.B
  235975. Heteroarenes 1, Part 2IK
  235976. Georg Thieme VerlagM
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  235979. 1H- and 2H-IsoindolesW
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  235983. 18839
  235984. Giuliano, R. M.B1Cycloaddition Reactions in Carbohydrate ChemistryCHSUBSTITUTED CYCLOPENTANE DERIVATIVES/DITHIOESTERS/PYRANOSIDES/DIENOPHILEK
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  235987. 2/28/96VM Intermolecular and Intramolecular Diels-Alder Reactions of Sugar DerivativesW
  235988. 1992X
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  235996. 2/28/96V:Pyrans and Fused Pyrans: (iii) Synthesis and Applications.W
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  236000. 18841
  236001. Osawa, E.//Yonemitsu, O.B7Carbocyclic Cage Compounds : Chemistry and ApplicationsK
  236002. VCH PublishersM
  236003. 19850N
  236004. 2/28/96V.Recent Developments in the Chemistry of CubaneW
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  236016. GABRIEL WEATHERHEADy
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  236022. 19852N
  236023. 2/28/96V Additions to N-Acyliminium Ions.W
  236024. 1991X
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  236026. GABRIEL WEATHERHEADy
  236027. Oxford
  236028. 18844
  236029. Brossi, A.B
  236030. The Alkaloids. Chem. and Pharm.K
  236031. Academic PressM
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  236033. 2/28/96V:N-Acyliminium ions as intermediates in alkaloid synthesis.W
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  236035. GABRIEL WEATHERHEADy
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  236038. Regitz, M.B
  236039. Carbenes (Carbenoids)K
  236040. Georg Thieme VerlagM
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  236047. GABRIEL WEATHERHEADy    Stuttgart
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  236050. Organophosphorus Compounds IIK
  236051. Georg Thieme VerlagM
  236052. 19855N
  236053. 2/28/96VePhosphorus(V) Compounds with Coordination Number 4: Phosphane Oxides, Sulfides, Selenides and  ImidesW
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  236056. GABRIEL WEATHERHEADy    Stuttgart
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  236058. Regitz, M.B
  236059. Organophosphorus Compounds IK
  236060. Georg Thieme VerlagM
  236061. 19856N
  236062. 2/28/96VLPhosphoru (III) Compounds with Coordination Number 3: Di- and PolyphosphanesW
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  236071. 2/28/96V8[m]Ferrocenophanes and multibridged [mn]Ferrocenophanes.W
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  236073. GABRIEL WEATHERHEADy
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  236076. Kropf, H.//Schaumann, E.B
  236077. Ene,X and Yne,X-CompoundsK
  236078. Georg Thieme VerlagM
  236079. 19858N
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  236084. GABRIEL WEATHERHEADy    Stuttga t
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  236087. Ene,X and Yne,X-CompoundsK
  236088. Georg Thieme VerlagM
  236089. 19859N
  236090. 2/28/96
  236091. 1-N-1-AlkynesW
  236092. 1993X    3267-3461Y
  236093. GABRIEL WEATHERHEADy    Stuttgart
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  236096. Ene,X an  Yne,X-CompoundsK
  236097. Georg Thieme VerlagM
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  236100. 1-Oxy-1-alkynesW
  236101. 1993X    3146-3267Y
  236102. GABRIEL WEATHERHEADy    Stuttgart
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  236107. 19861N
  236108. 2/28/96V3Cope, Oxy-Cope and Anionic Oxy-Cope Rearrangements.W
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  236110. GABRIEL WEATHERHEADy
  236111. Oxford
  236112. 18853
  236113. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC
  236114.  XADIAZOLINES /OXADIAZOLIDINESK
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  236118. 1,3,4-Oxadiazoles.W
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  236120. GABRIEL WEATHERHEADy
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  236122. 18854
  236123. Morrison, J. D.B>Asym etric Synthesis. Stereodifferentiating Reactions, Part A.
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  236125. 19863N
  236126. 2/28/96V2Chirality Transfer via Sigmatropic Rearrangements.W
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  236133. Jai Press, Inc.M
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  236135. 2/28/96VMOxidative Attachment of Arenesulfonyloxy Groups with Arenesulfonyl Peroxides.W
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  236137. GABRIEL WEATHERHEADy
  236138. Greenwich, CT
  236139. 18856
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  236142. Georg Thieme VerlagM
  236143. 19865N
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  236148. GABRIEL WEATHERHEADy    Stuttgart
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  236153. 19866N
  236154. 2/28/96V#Hydrosilylation of C=C and Alkynes.W
  236155. 1991X
  236156. GABRIEL WEATHERHEAD
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  236158. 18858
  236159. A    Falbe, J.B    AldehydesK
  236160. Georg Thieme VerlagM
  236161. 19867N
  236162. 2/28/96V2Preparation of Aldehydes from Aldehyde DerivativesW
  236163. 1983X
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  236165. GABRIEL WEATHERHEADy    Stuttgart
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  236167. Lindberg, T.B+Strategies and Tactics in Organic SynthesisK
  236168. Academic PressM
  236169. 19868N
  236170. 2/28/96VBTotal Synthesis of Taxusin: an Initial Step toward Taxol SynthesisW
  236171. 1991X
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  236173. GABRIEL WEATHERHEADy
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  236178. 19869N
  236179. 2/28/96V
  236180. Oxatriazoles and Thiatriazoles.W
  236181. 1984X
  236182. GABRIEL WEATHERHEADy
  236183. Oxford
  236184. 18861
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  236186. Pergamon PressM
  236187. 19870N
  236188. 2/28/96V
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  236191. GABRIEL WEATHERHEADy
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  236193. 18862
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  236195. Rev. Heteroatom Chem.C
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  236201. GABRIEL WEATHERHEADy
  236202. Tokyo, Japan
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  236204. Trost, B. M.//Fleming, I.B
  236205. Comprehensive Organic SynthesisC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[M+N]K
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  236207. 19872N
  236208. 2/28/96V
  236209. [4+3] Cycloadditions.W
  236210. 1991X
  236211. GABRIEL WEATHERHEADy
  236212. Oxford
  236213. 18864
  236214. Brossi, A.B
  236215. The Alkaloids. Chem. and Pharm.K
  236216. Academic PressM
  236217. 19873N
  236218. 2/28/96V2Lead tetraacetate oxidation in alkaloid synthesis.W
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  236220. GABRIEL WEATHERHEADy
  236221. New York
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  236224. DERIVATIVESK
  236225. Amer Chemical SocM
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  236227. 2/28/96VoDiels-Alder Cycloaddition to Unsaturated Sugars - Stereocontrol as a Function of Structure and  StereochemistryW
  236228. 1992X
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  236234. Photochemistry, Vol 23
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  236236. 19875N
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  236240. GABRIEL WEATHERHEADy
  236241. Cambridge, U. K.
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  236243. Brycesmith, D.//Gilbert, A.B
  236244. Photochemistry, Vol 23K
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  236246. 19876N
  236247. 2/28/96V Photolysis of Carbonyl CompoundsW
  236248. 1992X
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  236253. Brycesmith, D.//Gilbert, A.B
  236254. Photochemistry, Vol 23K
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  236256. 19877N
  236257. 2/28/96VQEnone Cycloadditions and Rearrangements - Photoreactions of Dienones and QuinonesW
  236258. 1992X
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  236263. Hudlicky, T.B)Organic Synthesis-Theory and ApplicationsK    Jai PressM
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  236274. 2/28/96V9Rearrangements of Vinylcyclopropanes and Related Systems.W
  236275. 1991X
  236276. GABRIEL WEATHERHEADy
  236277. Oxford
  236278. 18871
  236279. Trost, B. M.//Fleming, I.B
  236280. Comprehensive Organic SynthesisC
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  236283. 19880N
  236284. 2/28/96V[Reduction of Vinyl Halides to Alkenes, and of Aryl Halides and Related Compounds to Arenes.W
  236285. 1991X
  236286. GABRIEL WEATHERHEADy
  236287. Oxford
  236288. 18872
  236289. Snieckus, V.B&Advances in Carbanion Chemistry, Vol 1K
  236290. Jai Press IncM
  236291. 19881N
  236292. 2/28/96VLChiral Sulfinylallyl and alpha-Sulfinyl Ketimine Anions in Organic SynthesisW
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  236301. 2/28/96VoHighly Reactive  -Arene Iron Complexes and their Use in Stoichiometric and Catalytic Cyclic Addi ion Reactions.W
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  236303. GABRIEL WEATHERHEADy
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  236312. GABRIEL WEATHERHEADy
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  236315. Mayo, P. D.B,Rearrangements in Ground and Excited States.C,PHYSICAL ORGANIC /REARRANGEMENTS /CARBANIONSK
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  236325. Pergamon PressM
  236326. 19885N
  236327. 2/28/96VKNucleophilic Addition-Electrophilic Coupling with a Carbanion Intermediate.W
  236328. 1991X
  236329. GABRIEL WEATHERHEADy
  236330. Oxford
  236331. 18877
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  236333. Adv. CycloadditionK
  236334. Jai Press, Inc.M
  236335. 19886N
  236336. 2/28/96V:Steric Course and Mechanism of 1,3-Dipolar Cycloadditions.W
  236337. 1988Z
  236338. GABRIEL WEATHERHEADy
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  236341. Trost, B. M.//Fleming, I.B
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  236345. 19887N
  236346. 2/28/96VBReduction of C=X to CHXH by Dissolving Metals and Related Methods.W
  236347. 1991X
  236348. GABRIEL WEATHERHEADy
  236349. Oxford
  236350. 18879
  236351. Larson, G. L.B
  236352. Advances in Silicon Chemistry.C
  236353. SiK    Jai PressM
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  236363. 19889N
  236364. 2/28/96V1Practical Photochemistry: General Considerations.W
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  236369. Royal Society of ChemistryM
  236370. 19890N
  236371. 2/28/96V,Photoinitiated Free-Radical Chain Reactions.W
  236372. 1986X
  236373. GABRIEL WEATHERHEAD
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  236378. Pergamon PressM
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  236380. 2/28/96VEReduction of C=X to CH2 by Wolff-Kishner and Other Hydrazone Methods.W
  236381. 1991X
  236382. GABRIEL WEATHERHEADy
  236383. Oxford
  236384. 18883
  236385. Trost, B. M.//Fleming, I.B
  236386. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDEK
  236387. Pergamon Pre sM
  236388. 19892N
  236389. 2/28/96V+Reduction of C=N to CHNH by Metal Hydrides.W
  236390. 1991X
  236391. GABRIEL WEATHERHEADy
  236392. Oxford
  236393. 18884
  236394. Trost, B. M.//Fleming, I.B
  236395. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APPENDAGES /1,2-ADDITIONK
  236396. Pergamon PressM
  236397. 19893N
  236398. 2/28/96VaCarbanions of Alkali and Alkaline Ea th Cations: (ii) Selectivity of Carbonyl Addition Reactions.W
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  236400. GABRIEL WEATHERHEADy
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  236402. 18885
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  236407. 2/28/96VKReduction of organic functions via SmI2-promoted electron transfer process.W
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  236409. GABRIEL WEATHERHEADy
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  236412. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC]THIOPYRANS /BENZOTHIOPYRANS /THIOXANTHENES /DIBENZOTHIOPYRANS /THIABENZENES  /THIANES /THIINSK
  236413. Pergamon PressM
  236414. 19895N
  236415. 2/28/96V Thiopyrans and Fused Thiopyrans.W
  236416. 1984X
  236417. GABRIEL WEATHERHEADy
  236418. Oxford
  236419. 18887
  236420. Trost, B. M.//Fleming, I.B
  236421. Comprehensive Organic SynthesisC
  236422. FUNCTIONAL GROUPS /REDUCTIONK
  236423. Pergamon PressM
  236424. 19896N
  236425. 2/28/96V0Reduction of Saturated Alkyl Halides to Alkanes.W
  236426. 1991X
  236427. GABRIEL WEATHERHEADy
  236428. Oxford
  236429. 18888
  236430. Trost, B. M.//Fleming, I.B
  236431. Comprehensive Organic SynthesisC
  236432. ORGANOMETALLICS /CERIUM /CeK
  236433. Pergamon PressM
  236434. 19897N
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  236437. 1991X
  236438.  231Z
  236439. GABRIEL WEATHERHEADy
  236440. Oxford
  236441. 18889
  236442. Oae, S.B
  236443. Rev. Heteroatom Chem.C
  236444. MYU K.K.M
  236445. 19898N
  236446. 2/28/96V'New synthetic methods with lanthanides.W
  236447. 1990Z
  236448. GABRIEL WEATHERHEADy
  236449. Tokyo, Japan
  236450. 18890
  236451. ?A"Ogura, H.//Hasegawa, A.//Suami, T.B
  236452. CarbohydratesK
  236453. Kodansha LtdM
  236454. 19899N
  236455. 2/28/96V0Synthesis of Biologically Active Sialo-CompoundsW
  236456. 1992X
  236457. 267-281a
  236458. GABRIEL WEATHERHEADy
  236459. Tokyo
  236460. 18891
  236461. Atta-ur-rahman//Basha, F. Z.BOStudies in Natural Products Chemistry, Vol 13 : Bioactive Natural Products Pt AK
  236462. ElsevierM
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  236464. 2/28/96VtAsymmetric Synthesis of Bioactive Natural Prod cts and Related Compounds from Chiral Propane-1,3-Diols and AnaloguesW
  236465. 1993X
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  236467. GABRIEL WEATHERHEADy
  236468. Amsterdam, Netherlands
  236469. 18892
  236470. Klamann, D.B
  236471. Organotellurium CompoundsK
  236472. Georg Thieme VerlagM
  236473. 19901N
  236474. 2/28/96V?3- and 4-Membered Ring Systems with at Least One Tellurium AtomW
  236475. 1990X
  236476. 726-727Y
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  236478. GABRIEL WEATHERHEADy    Stuttgart
  236479. 18893
  236480. Klamann, D.B
  236481. Organotellurium CompoundsK
  236482. Georg Thieme VerlagM
  236483. 19902N
  236484. 2/28/96VSBis(aminocarbonyl), Bis(hydrazi othiocarbonyl), and Dibenzoyl Ditellurium CompoundsW
  236485. 1990X
  236486. 511-512Y
  236487. E12ba
  236488. GABRIEL WEATHERHEADy    Stuttgart
  236489. 18894
  236490. Klamann, D.B
  236491. Organotellurium CompoundsK
  236492. Georg Thieme VerlagM
  236493. 19903N
  236494. 2/28/96V#Polymeric Organotellurium CompoundsW
  236495. 1990X
  236496. 721-725Y
  236497. E12ba
  236498. GABRIEL WEATHERHEADy    Stuttgart
  236499. 18895
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  236501. Organotellurium CompoundsK
  236502. Georg Thieme VerlagM
  236503. 19904N
  236504. 2/28/96V Telluronic Acids and DerivativesW
  236505. 1990X
  236506. 364-365Y
  236507. E12ba
  236508. GABRIEL WEATHERHEADy    Stuttgart
  236509. 18896
  236510. Klamann, D.B
  236511. Organotellurium CompoundsK
  236512. Georg Thieme VerlagM
  236513. 19905N
  236514. 2/28/96V$Diorganotellurium Compounds (R-Te-R)W
  236515. 1990X
  236516. 370-493Y
  236517. E12ba
  236518. GABRIEL WEATHERHEADy    Stuttgart
  236519. 18897
  236520. Klamann, D.B
  236521. Organotellurium CompoundsK
  236522. Georg Thieme VerlagM
  236523. 19906N
  236524. 2/28/96V'Derivatives of Tellurous Acid [Te(OH)4]W
  236525. 1990X
  236526. 68-118Y
  236527. E12ba
  236528. GABRIEL WEATHERHEADy    Stuttgart
  236529. 18898
  236530. Klamann, D.B
  236531. Organotellurium CompoundsK
  236532. Georg Thieme VerlagM
  236533. 19907N
  236534. 2/28/96V3Acyl Organotellurium (Te-organotellurocarboxylates)W
  236535. 1990Y
  236536. E12ba
  236537. GABRIEL WEATHERHEADy    Stuttgart
  236538. 18899
  236539. Klamann, D.B
  236540. Organotellurium CompoundsK
  236541. Georg Thieme VerlagM
  236542. 19908N
  236543. 2/28/96V
  236544. TriorganotelluriumW
  236545. 1990X
  236546. 676-706Y
  236547. E12ba
  236548. GABRIEL WEATHERHEADy    Stuttgart
  236549. 18900
  236550. IB&Organotellurium Compounds  Klamann, D.K
  236551. Georg Thieme VerlagM
  236552. 19909N
  236553. 2/28/96V!6-Membered Tellurium HeteroarenesW
  236554. 1990X
  236555. 801-866Y
  236556. E12ba
  236557. GABRIEL WEATHERHEADy    Stuttgart
  236558. 18901
  236559. Klamann, D.B
  236560. Organotellurium CompoundsK
  236561. Georg Thieme VerlagM
  236562. 19910N
  236563. 2/28/96V.Diorganotellurium Oxides and Their DerivativesW
  236564. 1990X
  236565. 524-673Y
  236566. E12ba
  236567. GABRIEL WEATHERHEADy    Stuttgart
  236568. 18902
  236569. Klamann, D.B
  236570. Organotellurium CompoundsK
  236571. Georg Thieme VerlagM
  236572. 19911N
  236573. 2/28/96V!5-Membered Tellurium HeteroarenesW
  236574. 1990X
  236575. 728-800Y
  236576. E12ba
  236577. GABRIEL WEATHERHEADy    Stuttgart
  236578. 18903
  236579. Klamann, D.B
  236580. Organotellurium CompoundsK
  236581. Georg Thieme VerlagM
  236582. 19912N
  236583. 2/28/96V%Tellurium Compounds with a C=Te GroupW
  236584. 1990X
  236585. 512-523Y
  236586. E12ba
  236587. GABRIEL WEATHERHEADy    Stuttgart
  236588. 18904
  236589. 19913
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  236591. GABRIEL WEATHERHEAD
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  236593. Klamann, D.B
  236594. Organotellurium CompoundsK
  236595. Georg Thieme VerlagM
  236596. 19914N
  236597. 2/28/96V!Diorganotellurium Cyamide X SaltsW
  236598. 1990X
  236599. 674-675Y
  236600. E12ba
  236601. GABRIEL WEATHERHEADy    Stuttgart
  236602. 18906
  236603. Klamann, D.B
  236604. Organotellurium Compoun sK
  236605. Georg Thieme VerlagM
  236606. 19915N
  236607. 2/28/96V'Organotellurium Compounds: IntroductionW
  236608. 1990X
  236609. XXVI-XLIY
  236610. E12ba
  236611. GABRIEL WEATHERHEADy    Stuttgart
  236612. 18907
  236613. Klamann, D.B
  236614. Organotellurium CompoundsK
  236615. Georg Thieme VerlagM
  236616. 19916N
  236617. 2/28/96VEOrganotellurium Cyanides and Tellurium Dicyanides [R-Te-CN / Te(CN)2]W
  236618. 1990X
  236619. 366-370Y
  236620. E12ba
  236621. GABRIEL WEATHERHEADy    Stuttgart
  236622. 18908
  236623. Klamann, D.K
  236624. Georg Thieme VerlagM
  236625. 19917N
  236626. 2/28/96V;Tellurinic Acids and Derivatives  Organotellurium CompoundsW
  236627. 1990X
  236628. 298-359Y
  236629. E12ba
  236630. GABRIEL WEATHERHEADy    Stuttgart
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  236632. Klamann, D.B
  236633. Organotellurium CompoundsK
  236634. Georg Thieme VerlagM
  236635. 19918N
  236636. 2/28/96V+Organotetrahalotellurates (IV) [R-Te-Hal4]+
  236637. 1990X
  236638. 359-364Y
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  236640. GABRIEL WEATHERHEADy    Stuttgart
  236641. 18910
  236642. Klamann, D.B
  236643. Organotellurium CompoundsK
  236644. Georg Thieme VerlagM
  236645. 19919N
  236646. 2/28/96V
  236647. Bis(alkoxycarbonyl)telluriumsW
  236648. 1990X
  236649. 505-506Y
  236650. E12ba
  236651. GABRIEL WEATHERHEADy    Stuttgart
  236652. 18911
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  236654. Organotellurium CompoundsK
  236655. Georg Thieme VerlagM
  236656. 19920N
  236657. 2/28/96V
  236658. Tellurols (R-TeH)W
  236659. 1990X
  236660. 150-153Y
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  236662. GABRIEL WEATHERHEADy    Stuttgart
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  236666. Georg Thieme VerlagM
  236667. 19921N
  236668. 2/28/96V*Tellurenic Acids and Derivatives (R-Te-OH)W
  236669. 1990X
  236670. 237-297Y
  236671. E12ba
  236672. GABRIEL WEATHERHEADy    Stuttgart
  236673. 18913
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  236675. Organotellurium CompoundsK
  236676. Georg Thieme VerlagM
  236677. 19922N
  236678. 2/28/96V+Derivatives of Telluroxylic Acid (HO-Te-OH)W
  236679. 1990X
  236680. 1-68Y
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  236682. GABRIEL WEATHERHEADy    Stuttgart
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  236684. Klamann, D.B
  236685. Organotellurium CompoundsK
  236686. Georg Thieme VerlagM
  236687. 19923N
  236688. 2/28/96V8Triaryltrifluorotellurium (Triaryltellurium Trifluoride)
  236689. 1990X
  236690. E12ba
  236691. GABRIEL WEATHERHEADy    Stuttgart
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  236695.  Georg Thieme VerlagM
  236696. 19924N
  236697. 2/28/96V&Derivatives of Telluric Acid [Te(OH)6]W
  236698. 1990X
  236699. 118-150Y
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  236705. Georg Thieme VerlagM
  236706. 19925N
  236707. 2/28/96V
  236708. Tellurocyanates (R-Te-OCN)W
  236709. 1990X
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  236712. GABRIEL WEATHERHEADy    Stuttgart
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  236715. Organotellurium CompoundsK
  236716. Georg Thieme VerlagM
  236717. 19926N
  236718. 2/28/96V:alpha-X-Alkyl (or alpha-X-Alkenyl) A yltellurium CompoundsW
  236719. 1990X
  236720. 493-498Y
  236721. E12ba
  236722. GABRIEL WEATHERHEADy    Stuttgart
  236723. 18918
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  236725. Organotellurium CompoundsK
  236726. Georg Thieme VerlagM
  236727. 19927N
  236728. 2/28/96VVTetraorganotelluriums, Alkylidenediorganotellurium Compounds, and HexaorganotelluriumsW
  236729. 1990X
  236730. 707-721Y
  236731. E12ba
  236732. GABRIEL WEATHERHEADy    Stuttgart
  236733. 18919
  236734. Klamann, D.B
  236735. Organotellurium CompoundsK
  236736. Georg Thieme Verlag
  236737. 19928N
  236738. 2/28/96V!7-Membered Telluri m HeteroarenesW
  236739. 1990X
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  236741. GABRIEL WEATHERHEADy    Stuttgart
  236742. 18920
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  236745. Georg Thieme VerlagM
  236746. 19929N
  236747. 2/28/96V%Reactions of Organic Peroxo CompoundsW
  236748. 1988X
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  236756. 2/28/96VURecent advances in carbon-carbon bond forming reactions u ing alpha-thiocarbocations.W
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  236763. Georg Thieme VerlagM
  236764. 19931N
  236765. 2/28/96V
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  236773. Georg Thieme VerlagM
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  236777. 1990X
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  236784. Georg Thieme VerlagM
  236785. 19933N
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  236787. Diacyltellurium CompoundsW
  236788. 1990X
  236789. 506-511Y
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  236797. 2/28/96V(Organo(dihalo)tellurates(II) (R-TeHal2)+W
  236798. 1990X
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  236802. 18926
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  236804. Synthesis of Peptides Part IIK
  236805. Georg Thieme VerlagM
  236806. 19935N
  236807. 2/28/96V6Tests for Racemization of Peptide Construction MethodsW
  236808. 1974X
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  236814. Synthesis of Peptides Part IIM
  236815. 19936N
  236816. 2/28/96V7Tests for Purity and Purification of Synthetic PeptidesW
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  236820. GABRIEL WEATHERHEADy    Stuttgart
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  236823. The Alkaloids. Chem. and Pharm.K
  236824. Academic PressM
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  236834. 2/28/96VfBis-Heteroannulation - Total Synthesis of Furanoterpenes, Butenolides, Lactones and Related  MaterialsW
  236835. 1992X
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  236837. GABRIEL WEATHERHEADy    Greenwich
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  236842. 2/28/96V!The Total Synthesis of Saxitoxin.W
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  236849. 2/28/96VFLaser flash photolysis studies of ylide-forming reactions of carbenes.W
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  236851. GABRIEL WEATHERHEADy
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  236855. Academic PressM
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  236857. 2/28/96V1Synthesis of Tylonolide, The Aglycone of Tylosin.W
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  236862. 2/28/96V9Structures of Lithium Enolates and Phenolates in SolutionW
  236863. 1992a
  236864. GABRIEL WEATHERHEAD
  236865. 18934
  236866. Regitz, M.B
  236867. Organophosphorus Compounds IK
  236868. Georg Thieme VerlagM
  236869. 19943N
  236870. 2/28/96
  236871. kV,Phosphorus(IV) Compounds (Phosphonium Sa ts)W
  236872. 1982X
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  236877. Organic Nitrogen Compounds IK
  236878. Georg Thieme VerlagM
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  236881. Organic HydrazinesW
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  236887. Hartley, F. R.B8The Use of Organometallic Compound Organic in Synthesis.C
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  236890. 2/28/96V4Use of Organorhodium Compounds in Organic Synthesis.W
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  236899. 2/28/96V&Mechanism of Homogeneous HydrogenationW
  236900. 1987X    1049-1071Z
  236901. GABRIEL WEATHERHEADy
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  236907. 2/28/96V,Organonickel Compounds in Organic Synthesis.W
  236908. 1982Z
  236909. GABRIEL WEATHERHEAD
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  236912. Trost, B. M.//Fleming, I.B
  236913. Comprehensive Organic SynthesisC,FUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDESK
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  236916. 2/28/96V=Reduction of Carboxylic Acids to Aldehydes by Metal Hydrides.W
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  236937. Oxford
  236938. 18942
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  236947. 18943
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  236958. Asymmetric Synthesis.CgREAGENTS /BIO RANSFORMATION /STEREOCHEMISTRY /ENZYMES /REDUCTION OXIDATION HYDROLYSIS  ENANTIOSELECTIVEK
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  236992. Georg Thieme VerlagM
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  237012. 2/28/96VKPhotoinduced electron transfer in flexible biaryl donor acceptor molecules.W
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  237014. GABRIEL WEATHERHEADy
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  237018. Comprehensive Organic SynthesisC
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  237022. 2/28/96V:Reduction of C=X to CHXH Using Enzymes and Microorganisms.W
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  237024. GABRIEL WEATHERHEADy
  237025. Oxford
  237026. 18952
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  237028. Carbonic Acid DerivativesK
  237029. Georg Thieme VerlagM
  237030. 19961N
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  237037. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APPENDAGES /1,4-ADDITIONK
  237038. Pergamon PressM
  237039. 19962N
  237040. 2/28/96VDStabilized Nucleophiles with Electron Deficient Alkenes and Alkynes.W
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  237042. GABRIEL WEATHERHEADy
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  237044. 18954
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  237046. B,Strategies and Tactics in Organic Synthesis.K
  237047. Academic PressM
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  237050. Problem Solving in Organic Synthesis: the False Steps, Failed Pathways, and Ultimately Successful  Route to the Bottom Half of Ivermectin.W
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  237058. 2/28/96VARecent Studies of the Anomeric Effect: the Involvement of Sulfur.W
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  237060. GABRIEL WEATHERHEADy
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  237064. Asymmetric Synthesis.C/REAGENTS /STEREOCHEMISTRY /ASYMMETRIC CATALYSISK
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  237066. 2/28/96V(Chiral Ligands for Asymmetric Catalysis.W
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  237082. 2/28/96V>Functionalized tetraazamacrocycles: ligands with many aspects.W
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  237084. GABRIEL WEATHERHEADy
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  237090. 2/28/96V8Small-ring organo-silicon, germanium, and tin  ompounds.W
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  237100. 2/28/96V)Reduction of Nitro and Nitroso Compounds.W
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  237102. GABRIEL WEATHERHEADy
  237103. Oxford
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  237107. Georg Thieme VerlagM
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  237113. GABRIEL WEATHERHEADy    Stuttgart
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  237116. Organoboron Compounds IIIK
  237117. Georg Thieme VerlagM
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  237123. GABRIEL WEATHERHEADy    Stuttgart
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  237127. Georg Thieme VerlagM
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  237129. 2/28/96V_Organoboron Compounds with Threefold Coordinated Boron Atoms: Organoboron sigma- etal CompoundsW
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  237133. GABRIEL WEATHERHEADy    Stuttgart
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  237137. Georg Thieme VerlagM
  237138. 19973N
  237139. 2/28/96VjOrganoboron Compounds with Threefold Coordinated Boron Atom: Organoboron Phosphorus and  Arsenic CompoundsW
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  237143. GABRIEL WEATHERHEADy    Stuttgart
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  237147. Georg Th eme VerlagM
  237148. 19974N
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  237153. GABRIEL WEATHERHEADy    Stuttgart
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  237157. Georg Thieme VerlagM
  237158. 19975N
  237159. 2/28/96
  237160. VbOrganoboron Compounds with Threefold Coordinated Boron Atoms: Organoboron Element (III)  CompoundsW
  237161. 1983X
  237162. 403-410Y
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  237164. GABRIEL WEATHERHEADy    Stuttgart
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  237167. Organoboron Compounds IIK
  237168. Georg Thieme VerlagM
  237169. 19976N
  237170. 2/28/96VbOrganoboron Compounds with Threefold Coordinated Boron Atoms: Cationic Organoboron(III)  CompoundsW
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  237174. GABRIEL WEATHERHEADy    Stuttgart
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  237178. Georg Thieme VerlagM
  237179. 19977N
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  237188. Georg Thieme VerlagM
  237189. 19978N
  237190. 2/28/96V`Organoboron Compounds with Threefold Coordinated Boron Atom: Organoboron Element (IV)  CompoundsW
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  237198. Georg Thieme VerlagM
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  237205. GABRIEL WEATHERHEADy    Stuttgart
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  237209. Georg Thieme VerlagM
  237210. 19980N
  237211. 2/28/96VYOrganoboron Compounds with Threefold Coordinated Boron Atom: Organoboron Oxygen CompoundsW
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  237215. GABRIEL WEATHERHEADy    Stuttgart
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  237219. Georg Thieme VerlagM
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  237229. Georg Thieme VerlagM
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  237235. GABRIEL WEATHERHEADy    Stuttgart
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  237246. GABRIEL WEATHERHEADy    Stuttgart
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  237262. GABRIEL WEATHERHEADy
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  237406. Oxford
  237407. 18993
  237408. Trost, B. M.//Fleming, I.B
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  237410. FUNCTIONAL GROUPS /REDUCTIONK
  237411. Pergamon PressM
  237412. 20002N
  237413. 2/28/96V:Partial Reduction of Enones, Styrenes and Related Systems.W
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  237415. GABRIEL WEATHERHEADy
  237416. Oxford
  237417. 18994
  237418. A)Noels, A. F.//Graziani, M.//Hubert, A. J.B/Metal Promoted Selectivity in Organic SynthesisK
  237419. Kluwer Academic PublM
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  237421. 2/28/96V@Industrial Aspects of Selectivity Applying Homogeneous CatalysisW
  237422. 1991X
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  237424. GABRIEL WEATHERHEADy
  237425. Dordrecht, Netherlands
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  237427. K eher, R. P.B
  237428. Hetarenes II, Part IK
  237429. Georg Thieme VerlagM
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  237435. GABRIEL WEATHERHEADy    Stuttgart
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  237441. 2/28/96V"Nucleophilic Coupling with Arynes.W
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  237443. GABRIEL WEATHERHEADy
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  237445. 18997
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  237453. GABRIEL WEATHERHEADy
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  237455. 18998
  237456. Trost, B. M.//Fleming, I.B
  237457. Comprehensive Organic Synthesis
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  237463. GABRIEL WEATHERHEADy
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  237469. 2/28/96V3Importance of Heterocycles in Biochemical Pathways.W
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  237473. 19000
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  237478. 2/28/96V
  237479. Alkene Synthesis.W
  237480. 1991X
  237481. GABRIEL WEATHERHEADy
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  237483. 19001
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  237485. Rev. Heteroatom Chem.C
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  237488. 2/28/96V<Sulfonyl mechanisms: Evidence for a stereoelectronic effect.W
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  237490. GABRIEL WEATHERHEADy
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  237496. 2/28/96V3New Developments in Macrocyclic Polyamine ChemistryW
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  237503. John Wiley & Sons LtdM
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  237506. Sulfur and Phosphorus PeroxidesW
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  237515. 20013N
  237516. 2/28/96V'The Aldol Reaction: Group III Enolates.W
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  237518. GABRIEL WEATHERHEADy
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  237524. 20014N
  237525. 2/28/96VMActivation of superoxide: organic synthesis using peroxysulfur intermediates.W
  237526. 1990Z
  237527. GABRIEL WEATHERHEADy
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  237529. 19006
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  237533. 20015N
  237534. 2/28/96V"Oxidation of Carbon-Halogen Bonds.W
  237535. 1991X
  237536. GABRIEL WEATHERHEADy
  237537. Oxford
  237538. 19007
  237539. Aitken, R. A.//Kilenyi, S. N.B
  237540. Asymmetric Synthesis
  237541. Chapman & HallM
  237542. 20016N
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  237544. Asymmetric Total SynthesisW
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  237551. 20017N
  237552. 2/28/96VGSome Chiral Approaches to Syntheses of Bioactive Indolizidine AlkaloidsW
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  237573. GABRIEL WEATHERHEADy    Stuttgart
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  237590. 1,2,3-Benzodithiazoium SaltsW
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  237593. GABRIEL WEATHERHEADy    Stuttgart
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  237600. 1,2,3-Dithiazolium SaltsW
  237601. 1994X
  237602. GABRIEL WEATHERHEADy    Stuttgart
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  237606. Georg Thieme VerlagM
  237607. 20023N
  237608. 2/28/96V
  237609. 1,3,2-Benzodithiazolium SaltsW
  237610. 1994X
  237611. GABRIEL WEATHERHEADy    Stuttgart
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  237614. Heteroarenes III, Part 4K
  237615. Georg Thieme VerlagM
  237616. 20024N
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  237618. 1,4,2-Dithiazoliu  SaltsW
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  237621. GABRIEL WEATHERHEADy    Stuttgart
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  237625. Georg Thieme VerlagM
  237626. 20025N
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  237628. Oxathiazolium CompoundsW
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  237631. GABRIEL WEATHERHEADy    Stuttgart
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  237646. 2/28/96V8The Bimolecular Aliphatic Mannich and Related Reactions.W
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  237648. GABRIEL WEATHERHEADy
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  237652. Organophosphorus Compounds IK
  237653. Georg Thieme VerlagM
  237654. 20028N
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  237683. Georg Thieme VerlagM
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  237694. Georg Thieme VerlagM
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  237707. 2/28/96V Oxidation of Carbon-Metal Bonds.W
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  237709. GABRIEL WEATHERHEADy
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  237713. Organic PeroxidesK
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  237728. GABRIEL WEATHERHEADy
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  237737. GABRIEL WEATHERHEADy
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  237754. GABRIEL WEATHERHEADy
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  237759. Georg Thieme VerlagM
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  237822. 1991X
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  238241. GABRIEL WEATHERHEADy
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  238332. 1984X
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  238335. 19093
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  238337. Georg Thieme VerlagM
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  238347. Georg Thieme VerlagM
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  238374. GABRIEL WEATHERHEADy    Stuttgart
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  238377. Georg Thieme VerlagM
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  238381. 1992X
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  238384. GABRIEL WEATHERHEADy    Stuttgart
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  238388. Georg Thieme VerlagM
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  238392. 1992X
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  239860. Amsterdam, Netherlands
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  239862. Trost, B. M.//Fleming, I.B
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  239866. 2/28/96V3Synthesis of Esters, Activated Esters and Lactones.W
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  239868. GABRIEL WEATHERHEADy
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  239871. Schaumann, E.B
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  239873. Georg Thieme VerlagM
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  239887. GABRIEL WEATHERHEADy
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  239890. Kreher, R. P.B
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  239892. Georg Thieme VerlagM
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  239902. 20273N
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  239912. 20274N
  239913. 2/28/96V.Xanthylium Salts (Dibenzo[b /e]pyrylium Salts)W
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  239922. 2/28/96V'Reduction with Organometallic CompoundsW
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  239930. Georg Thieme VerlagM
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  239932. 2/28/96V Reduction with Organic CompoundsW
  239933. 1981X
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  239940. 20277N
  239941. 2/28/96V:Reduction with Inorganic Reducing Agents:  Metal CarbonylsW
  239942. 1981X
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  239951. 2/28/96V5Reduction with Inorganic Reducing Agents: Metal SaltsW
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  239961. 2/28/96V4Reduction with Inorganic Reducing Agents: Non MetalsW
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  239969. Georg Thieme VerlagM
  239970. 20280N
  239971. 2/28/96V0Reduction with Inorganic Reducing Agents: MetalsW
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  239973. 613-743Y
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  239984. GABRIEL WEATHERHEADy
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  240000. 2/28/96VESome synthetically useful reactions of elemental sulfur and selenium.W
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  240002. GABRIEL WEATHERHEADy
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  240006. Elsevier Science Publ B VM
  240007. 20284N
  240008. 2/28/96V-Conformational Control in Macrolide SynthesisW
  240009. 1992X
  240010. 151-180a
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  240012. Amsterdam, Netherlands
  240013. 19276
  240014. Trost, B. M.//Fleming, I.B
  240015. Comprehensive Organic SynthesisC&C-C BOND FORMATION /ANNULATION /3-RINGK
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  240017. 20285N
  240018. 2/28/96VAFormation and Further Transformations of 1,1-Dihalocyclopropanes.
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  240020. GABRIEL WEATHERHEADy
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  240022. 19277
  240023. Ando, W.B
  240024. Organic PeroxidesK
  240025. John Wiley & Sons LtdM
  240026. 20286N
  240027. 2/28/96V,Formation of Organoperoxides from SuperoxideW
  240028. 1992X
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  240036. 2/28/96V
  240037. Organoboron Compounds.W
  240038. 1982Z
  240039. GABRIEL WEATHERHEADy
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  240042. Mayo, P. D.B,Rearrangements in Ground and Excited States.CWPHYSICAL ORGANIC /REARRANGEMENTS /PHOTOCHEMICAL REACTIONS /PHOTOCHEMISTRY  /CARBRING /3K
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  240044. 2/28/96V<Photochemical Rearrangements Involving Three Membered Rings.W
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  240046. GABRIEL WEATHERHEADy
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  240050. Jai Press, Inc.M
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  240052. 2/28/96V/Radical Kinetics and Mechanistic Probe Studies.W
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  240054. GABRIEL WEATHERHEADy
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  240062.  etrazines and Pentazines.W
  240063. 1984X
  240064. GABRIEL WEATHERHEADy
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  240067. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC+TRIAZINES /BENZOTRIAZINES /NAPHTHOTRIAZINESK
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  240069. 20291N
  240070. 2/28/96V,1,2,4-Triazines and their Benzo Derivatives.W
  240071. 1984X
  240072. GABRIEL WEATHERHEADy
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  240074. 19283
  240075. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC+TRIAZINES /BENZOTRIAZINES /NAPHTHOTRIAZINESK
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  240077. 20292N
  240078. 2/28/96V,1,2,3-Tri zines and their Benzo Derivatives.W
  240079. 1984X
  240080. GABRIEL WEATHERHEADy
  240081. Oxford
  240082. 19284
  240083. Regitz, M.B
  240084. Organophosphorus Compounds IK
  240085. Georg Thieme VerlagM
  240086. 20293N
  240087. 2/28/96V_Phosphorus(III)Compounds with Coordination / Number 3: Phosphonous Acids and Their  DerivativesW
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  240095. 2/28/96VHZirconocene-alkene complexes: their formation, structure, and reactions.W
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  240097. GABRIEL WEATHERHEADy
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  240107. GABRIEL WEATHERHEADy
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  240109. 19287
  240110. Liebeskind, L. S.B
  240111. Adv. Metal-Organic Chem.C^FUNCTIONAL GROUPS /PREPARATIONS /ALKENES /ORGANOMETALLICS /ELEMENT /NICKEL  /PALLADIUM /Ni /PdK
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  240113. 20296N
  240114. 2/28/96VIMetal-Organic Approach to Stereoselective Synthesis of Exocyclic Alkenes.W
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  240116. GABRIEL WEATHERHEADy
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  240131. 2/28/96V'Heterocyclic Rings containing Halogens.W
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  240140. 2/28/96V#Carbonyl Compounds: alpha-Cleavage.W
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  240146. Pergamon PressM
  240147. 20300N
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  240151. GABRIEL WEATHERHEADy
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  240154. Osawa, E.//Yonemitsu, O.B7Carbocyclic Cage Compounds : Chemistry and ApplicationsK
  240155. VCH PublishersM
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  240159. 1992X
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  240168. 2/28/96VGPreparation of Conjugated Dienes and Enynes via Organo Copper Reagents.W
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  240170. GABRIEL WEATHERHEADy
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  240174. Modern Synthetic Methods.CZORGANOMETALLICS /MANGANESE /O=C-X /Cl /C-X /Mn /SUBSTITUTION /Cl BY C /O=C-R  /KETONES /MnK
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  240177. 2/28/96V9Organomanganous Reagents: Their Use in Organic Synthesis.W
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  240188. 1991Z
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  240196. 1993Z
  240197. GABRIEL WEATHERHEADy
  240198. Oxford, U.K.
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  240200. Trost, B. M.//Fleming, I.B
  240201. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /REDUCTION /METAL HYDRIDEK
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  240204. 2/28/96V?Reduction of C=X to CHXH by Chirally Modified Hydride Reagents.W
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  240206. GABRIEL WEATHERHEADy
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  240210. Organometallics. A ManualC
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  240212. 20307N
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  240221. Modern Synthetic Methods.CPC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /ORGANOMETALLICS /GENERALK
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  240225. 1989Z
  240226. GABRIEL WEATHERHEADy
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  240230. Comprehensive Organic SynthesisC.C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGEK
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  240233. 2/28/96V)Nucleophilic Coupling with Aryl Radicals.W
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  240235. GABRIEL WEATHERHEADy
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  240238. Trost, B. M.//Fleming, I.B
  240239. Comprehensive Or anic SynthesisC2FUNCTIONAL GROUPS /PREPARATIONS /MISCELLANEOUS /SeK
  240240. Pergamon PressM
  240241. 20310N
  240242. 2/28/96V%Selenoesters of all Oxidation States.W
  240243. 1991X
  240244. GABRIEL WEATHERHEADy
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  240248. Rev. Heteroatom Chem.C
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  240251. 2/28/96V'Hypervalent alkyliodine(III) chemistry.W
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  240253. GABRIEL WEATHERHEADy
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  240258. Pergamon PressM
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  240260. 2/28/96V5Nucleophilic Addition to Carboxylic Acid Derivatives.W
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  240265. Bartl, H.//Falbe, J.B
  240266. Macromolecular MaterialsK
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  240275. Asymmetr c SynthesisCiFUNCTIONAL GROUPS /TRANSFORMATIONS /C=C TO X-C-C-Y /HYDROMETALLATION /Si  /CARBONYLATION ENANTIOSELECTIVEK
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  240298. GABRIEL WEATHERHEADy
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  240302. CarbohydratesK
  240303. Kodansha LtdM
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  240484. GABRIEL WEATHERHEADy
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  240587. 1992X
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  240612. GABRIEL WEATHERHEADy
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  240630. 1983X
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  240804. Georg Thieme VerlagM
  240805. 20373N
  240806. 2/28/96V8Organosilicon Compounds as Reagents in Organic ChemistryW
  240807. 1980X
  240808. 339-391Y
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  240810. GABRIEL WEATHERHEADy    Stuttgart
  240811. 19365
  240812. Bayer, O.//M ller, E.B
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  240814. Georg Thieme VerlagM
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  240816. 2/28/96V%Organosilicon Compounds: IntroductionW
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  240820. GABRIEL WEATHERHEADy    Stuttgart
  240821. 19366
  240822. Kropf, H.//Schaumann, E.B
  240823. Ene,X and Yne,X-CompoundsK
  240824. Georg Thieme VerlagM
  240825. 20375N
  240826. 2/28/96V
  240827. 1-Hetero-1-metalloxy-1-alkenesW
  240828. 1993X    1289-1324Y
  240829. GABRIEL WEATHERHEADy    Stuttgart
  240830. 19367
  240831. Trost, B. M.//Fleming, I.B
  240832. Comprehensive Organic SynthesisC.FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUS /BK
  240833. Pergamon PressM
  240834. 20376N
  240835. 2/28/96V Oxidation of Carbon-Boron Bonds.W
  240836. 1991X
  240837. GABRIEL WEATHERHEAD
  240838. Oxford
  240839. 19368
  240840. Trost, B. M.//Fleming, I.B
  240841. Comprehensive Organic SynthesisK
  240842. Pergamon PressM
  240843. 20377N
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  240845. Boron Stabilization.W
  240846. 1991X
  240847. GABRIEL WEATHERHEADy
  240848. Oxford
  240849. 19369
  240850. Mayo, P. D.B,Rearrangements in Ground and Excited States.C(ORGANOMETALLICS /BORON /REARRANGEMENT /BK
  240851. 20378N
  240852. 2/28/96V
  240853. Rearrangements Involving Boron.W
  240854. 1980X
  240855. GABRIEL WEATHERHEADy
  240856. New York
  240857. 19370
  240858. Trost, B. M.//Fleming, I.B
  240859. Comprehensive Organic SynthesisC*C-C BOND FORMATION /APPENDAGES /ALKYLATIONK
  240860. Pergamon PressM
  240861. 20379N
  240862. 2/28/96V7Nucleophiles with Cationic Pentadienyl-Metal Complexes.W
  240863. 1991X
  240864. GABRIEL WEATHERHEADy
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  240866. 19371
  240867. Liebeskind, L. S.B
  240868. Adv. Metal-Organic Chem.C)ORGANOMETALLICS /IRON /MOLYBDENUM /Mo /FeK
  240869. Jai Press, Inc.M
  240870. 20380N
  240871. 2/28/96V`Recent Developments in the Synthetic Applications of Organoiron and Organomolybdenum  Chemistry.W
  240872. 1989Z
  240873. GABRIEL WEATHERHEADy
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  240875. 19372
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  240877. 20381N
  240878. 2/28/96V>Transition Metal-Stabilized Carbocations in Organic Synthesis.W
  240879. 1987X
  240880. 889-978Z
  240881. GABRIEL WEATHERHEADy
  240882. Chichester
  240883. 19373
  240884. "B&Silicon Compounds,  egister and ReviewC
  240885. Petrarch SystemsM
  240886. 20382N
  240887. 2/28/96V
  240888. Silane blocking agents.W
  240889. 1987X
  240890. GABRIEL WEATHERHEADy
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  240892. 19374
  240893. #A1Liebman, J. F.//Greenberg, A.//Dolbier, W. R., JrB|Fluorine-Containing Molecules. Structure  Reactivity, Synthesis and Application (Molecular Structure and Energetics, Vol. 8)C
  240894. VCH PublishersM
  240895. 20383N
  240896. 2/28/96V+Structure and Bonding in N, O, F Compounds.W
  240897. 1988a
  240898. GABRIEL WEATHERHEADy
  240899. New York
  240900. 19375
  240901. Kropf, H.//Schaumann, E.B
  240902. Ene,X and Yne,X-CompoundsK
  240903. Georg Thieme VerlagM
  240904. 20384N
  240905. 2/28/96V
  240906. KeteniminesW
  240907. 1993X    2531-2710Y
  240908. GABRIEL WEATHERHEADy    Stuttgart
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  240911. Modern Synthetic Methods.
  240912. %CPC-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /ORGANOMETALLICS /GENERALK
  240913. SpringerM
  240914. 20385N
  240915. 2/28/96VCEnantioselective Catalysis with Chiral Cobalt and Copper Complexes.W
  240916. 1989Z
  240917. GABRIEL WEATHERHEADy
  240918. Berlin
  240919. 19377
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  240921. Rev. Heteroatom Chem.C
  240922. Se /TeK
  240923. MYU K.K.M
  240924. 20386N
  240925. 2/28/96VHSelenium and tellurium reagents. Preparation and sy thetic applications.W
  240926. 1989Z
  240927. GABRIEL WEATHERHEADy
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  240929. 19378
  240930. 'A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid DerivativesK
  240931. Georg Thieme VerlagM
  240932. 20387N
  240933. 2/28/96V\N-Alkyl/arylimidic Esters, Hydroximic Acids, Alkyl Hydrazonates, and 1-Alkoxy-1-diazoalkanesW
  240934. 1985X
  240935. 812-831Y
  240936. GABRIEL WEATHERHEADy    Stuttgart
  240937. 19379
  240938. (A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid DerivativesK
  240939. Georg Thieme VerlagM
  240940. 20388N
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  240942. Carboxylic AnhydridesW
  240943. 1985X
  240944. 633-656Y
  240945. GABRIEL WEATHERHEADy    Stuttgart
  240946. 19380
  240947. )A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid Derivatives
  240948. Georg Thieme VerlagM
  240949. 20389N
  240950. 2/28/96V4Carboxyli  Acid Amino Esters (O-Acyl Hydroxylamines)W
  240951. 1985X
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  240953. GABRIEL WEATHERHEADy    Stuttgart
  240954. 19381
  240955. *A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid DerivativesK
  240956. Georg Thieme VerlagM
  240957. 20390N
  240958. 2/28/96V
  240959. Carboxylic Acid EstersW
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  240962. GABRIEL WEATHERHEADy    Stuttgart
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  240964. Pletcher, D.B.Electochemistry. Specialist Periodical Rep rt.CTFUNCTIONAL GROUPS /TRANSFORMATIONS /ELECTROCHEMICAL REACTIONS /ELECTROCHEMISTRY  /TMK
  240965. Royal Society of ChemistryM
  240966. 20391N
  240967. 2/28/96V3The Electrochemistry of Transition Metal Complexes.W
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  240969. GABRIEL WEATHERHEAD
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  240972. Royal Society of ChemistryM
  240973. 20392N
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  240975. Alkenes: Photooxidation.W
  240976. 1986X
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  240980. -B$Photochemistry in Organic Synthesis.CKFUNCTIONAL GROUPS /TRANSFORMATIONS /PHOTOCHEMICAL REACTIONS /PHOTOCHEMISTRYK
  240981. Royal Society of ChemistryM
  240982. 20393N
  240983. 2/28/96V"Practical Photochemistry Scale  p.W
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  240985. GABRIEL WEATHERHEAD
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  240990. 20394N
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  240994. GABRIEL WEATHERHEADy
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  241000. 20395N
  241001. 2/28/96VBTwo Fused Five-membered Heterocyclic Rings: (i) Classical Systems.W
  241002. 1984X
  241003. GABRIEL WEATHERHEADy
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  241005. 19387
  241006. Trost, B. M.//Fleming, I.B
  241007. Comprehensive Organic SynthesisC=C-C BOND FORMAT ON /PERICYCLIC REACTIONS /SIGMATROPIC /[3 /3]K
  241008. Pergamon PressM
  241009. 20396N
  241010. 2/28/96V'Rearrangements of Divinylcyclopropanes.W
  241011. 1991X
  241012. GABRIEL WEATHERHEADy
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  241014. 19388
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  241017. 20397N
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  241019. Polymer Supported Catalysts.W
  241020. 1982X
  241021. GABRIEL WEATHERHEADy
  241022. Oxford
  241023. 19389
  241024. Trost, B. M.//Fleming, I.B
  241025. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  241027. 20398N
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  241029. Oxidation Adjacent to Nitrogen.W
  241030. 1991X
  241031. GABRIEL WEATHERHEADy
  241032. Oxford
  241033. 19390
  241034. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC#PYRAZINES /QUINOXALINES /PHENAZINESK
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  241036. 20399N
  241037. 2/28/96V&Pyrazines and their Benzo Derivatives.W
  241038. 1984X
  241039. GABRIEL WEATHERHEADy
  241040. Oxford
  241041. 19391
  241042. Trost, B. M.//Fleming, I.B
  241043. Comprehensive Organic SynthesisC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[2+2]K
  241044. Pergamon PressM
  241045. 20400N
  241046. 2/28/96V
  241047. The Paterno-Buchi Reaction.W
  241048. 1991X
  241049. GABRIEL WEATHERHEADy
  241050. Oxford
  241051. 19392
  241052. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryK
  241053. Pergamon PressM
  241054. 20401N
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  241056. 1,2,4-Triazoles.W
  241057. 1984X
  241058. GABRIEL WEATHERHEADy
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  241063. Pergamon PressM
  241064. 20402N
  241065. 2/28/96V>Synthesis of Five-membered Rings with Two or More Heteroatoms.W
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  241067. GABRIEL WEATHERHEADy
  241068. Oxford
  241069. 19394
  241070. Morrison, J. D.B
  241071. Asymmetric Synthes s
  241072. C-C BOND FORMATION /APPENDAGES /1,4-ADDITION /ENANTIOGENIC REACTIONS /C=C-X /SO  /C=C-SO /VINYL SULFOXIDES /ENANTIOSELECTIVE /CYCLOHEXANONES /CYCLOPENTANONES /SK
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  241074. 2/28/96VAAddition of Organometallic Reagents to Chiral Vinylic Sulfoxides.W
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  241076. GABRIEL WEATHERHEADy
  241077. New York
  241078. 19395
  241079. Ando, W.B
  241080. Organic PeroxidesK
  241081. John Wiley & Sons LtdM
  241082. 20404N
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  241085. 1992X
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  241087. GABRIEL WEATHERHEADy
  241088. Chichester, U. K.
  241089. 19396
  241090. Trost, B. M.//Fleming, I.B
  241091. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
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  241093. 20405N
  241094. 2/28/96V:Oxidation Adjacent to Oxygen o  Alcohols by Other Methods.W
  241095. 1991X
  241096. GABRIEL WEATHERHEADy
  241097. Oxford
  241098. 19397
  241099. :A"Ogura, H.//Hasegawa, A.//Suami, T.B
  241100. CarbohydratesK
  241101. Kodansha LtdM
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  241103. 2/28/96V[Synthesis of Oligosaccharides Related to Plant, Vertebrate, and Bacterial Cell-Wall GlycansW
  241104. 1992X
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  241106. GABRIEL WEATHERHEADy
  241107. Tokyo, Japan
  241108. 19398
  241109. Kropf, H.//Schaumann, E.B
  241110. Ene,X and Yne,X-CompoundsK
  241111. Georg Thieme VerlagM
  241112. 20407N
  241113. 2/28/96V
  241114. Ene-N- ompoundsW
  241115. 1993X
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  241117. GABRIEL WEATHERHEADy    Stuttgart
  241118. 19399
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  241120. Georg Thieme VerlagM
  241121. 20408N
  241122. 2/28/96VJCatalytic Reactions: Hydrooxygenation, Hydrosulfonation and HydroaminationW
  241123. 1986X    1022-1041Y
  241124. GABRIEL WEATHERHEADy    Stuttgart
  241125. 19400
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  241127. Heteroarenes I, Part 2K
  241128. Georg Thieme VerlagM
  241129. 20409N
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  241131. 1-Benzofurans (Benzo[b]furans)W
  241132. 1994X
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  241134. GABRIEL WEATHERHEADy    Stuttgart
  241135. 19401
  241136. Kreher, R. P.B
  241137. Heteroarenes II, Part 2K
  241138. Georg Thieme VerlagM
  241139. 20410N
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  241141. Benzo[c]quinolizinium SaltsW
  241142. 1992X
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  241144. GABRIEL WEATHERHEADy    Stuttgart
  241145. 19402
  241146. Kreher, R. P.B
  241147. Heteroarenes II, Part 2K
  241148. Georg Thieme VerlagM
  241149. 20411N
  241150. 2/28/96V
  241151. Ben o[a]quinolizinium SaltsW
  241152. 1992X
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  241154. GABRIEL WEATHERHEADy    Stuttgart
  241155. 19403
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  241158. Pergamon PressM
  241159. 20412N
  241160. 2/28/96V
  241161. 1,3,5-Triazines.W
  241162. 1984X
  241163. GABRIEL WEATHERHEADy
  241164. Oxford
  241165. 19404
  241166. Oae, S.B
  241167. Rev. Heteroatom Chem.C
  241168. MYU K.K.M
  241169. 20413N
  241170. 2/28/96VRUnusual properties of phosphorus functions in the 7-phosphanorbornene ring system.W
  241171. 1990Z
  241172. GABRIEL WEATHERHEADy
  241173. Tokyo, Japan
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  241176. BENZOTHIOPHENES /THIOPHYNESK
  241177. Pergamon PressM
  241178. 20414N
  241179. 2/28/96V8Thiophenes and their Benzo Derivatives: (ii) Reactivity.W
  241180. 1984X
  241181. GABRIEL WEATHERHEADy
  241182. Oxford
  241183. 19406
  241184. Lindberg, T.B+Strategies and Tactics in Organic SynthesisK
  241185. Academic PressM
  241186. 20415N
  241187. 2/28/96V)Total Synthesis of the FK506/FKBP ComplexW
  241188. 1991X
  241189. 495-534Z
  241190. GABRIEL WEATHERHEAD
  241191. San Diego, CA
  241192. 19407
  241193. Kropf, H.//Schaumann, E.B
  241194. Ene,X and Yne,X-CompoundsK
  241195. Georg Thieme VerlagM
  241196. 20416N
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  241198. 1,2-Di-N-1-alkenesW
  241199. 1993X    1325-1382Y
  241200. GABRIEL WEATHERHEADy    Stuttgart
  241201. 19408
  241202. Trost, B. M.//Fleming, I.B
  241203. Comprehensive Organic SynthesisC>FUNCTIONAL GROUPS /OXIDATION / LKENES AND ALKYNES /EPOXIDATIONK
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  241205. 20417N
  241206. 2/28/96V]Addition Reactions with Formation of Carbon-Oxygen Bonds: (i) General Methods of Epoxidation.W
  241207. 1991X
  241208. GABRIEL WEATHERHEADy
  241209. Oxford
  241210. 19409
  241211. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic Chemistry
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  241213. Pergamon PressM
  241214. 20418N
  241215. 2/28/96VGTwo Fused Five-membered Heterocyclic Rings: (ii) Non-classical Systems.W
  241216. 1984X
  241217. 1027Z
  241218. GABRIEL WEATHERHEADy
  241219. Oxford
  241220. 19410
  241221. Trost, B. M.//Fleming, I.B
  241222. Comprehensive Organic SynthesisC:C-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITION /ZnK
  241223. Pergamon P essM
  241224. 20419N
  241225. 2/28/96V4Zinc Enolates: the Reformatsky and Blaise Reactions.W
  241226. 1991X
  241227. GABRIEL WEATHERHEADy
  241228. Oxford
  241229. 19411
  241230. Hagemann, H.//Klamann, D.B
  241231. O/N-AcetalsK
  241232. Georg Thieme VerlagM
  241233. 20420N
  241234. 2/28/96
  241235. HV(OR/N-Acetals with Linear O-C-N StructureW
  241236. 1991X
  241237. 89-295Y
  241238. E14a/2a
  241239. GABRIEL WEATHERHEADy    Stuttgart
  241240. 19412
  241241. Hagemann, H.//Klamann, D.B
  241242. O/N-AcetalsK
  241243. Georg Thieme VerlagM
  241244. 20421N
  241245. 2/28/96V(OH/N Acetals with Linear O-C-N StructureW
  241246. 1991X
  241247. 1-75Y
  241248. E14a/2a
  241249. GABRIEL WEATHERHEADy    Stuttgart
  241250. 19413
  241251. Hagemann, H.//Klamann, D.B
  241252. O/N-AcetalsK
  241253. Georg Thieme VerlagM
  241254. 20422N
  241255. 2/28/96V%O/N-Acetals with Cyclic C-O StructureW
  241256. 1991X
  241257. 295-402Y
  241258. E14a/2a
  241259. GABRIEL WEATHERHEADy    Stuttgart
  241260. 19414
  241261. Hagemann, H.//Klamann, D.B
  241262. O/N-AcetalsK
  241263. Georg Thieme VerlagM
  241264. 20423N
  241265. 2/28/96V(OX/N-Acetals with Linear O-C-N StructureW
  241266. 1991X
  241267. 76-89Y
  241268. E14a/2a
  241269. GABRIEL WEATHERHEADy    Stuttgart
  241270. 19415
  241271. Hagemann, H.//Klamann, D.B
  241272. O/N-AcetalsK
  241273. Georg Thieme VerlagM
  241274. 20424N
  241275. 2/28/96V'O/N-Acetals with Cyclic O-C-N StructureW
  241276. 1991X
  241277. 513-819Y
  241278. E14a/2a
  241279. GABRIEL WEATHERHEADy    Stuttgart
  241280. 19416
  241281. Hagemann, H.//Klamann, D.B
  241282. O/N-AcetalsK
  241283. Georg Thieme Verlag
  241284. 20425N
  241285. 2/28/96V%O/N-Acetals with Cyclic C-N StructureW
  241286. 1991X
  241287. 403-512Y
  241288. E14a/2a
  241289. GABRIEL WEATHERHEADy    Stuttgart
  241290. 19417
  241291. Larson, G. L.B
  241292. Adv. Silicon ChemistryC&ORGANOMETALLICS /SILICON /REAGENTS /SiK
  241293. Jai Press, Inc.M
  241294. 20426N
  241295. 2/28/96V&The Chemistry of Cyanotrimethylsilane.W
  241296. 1991Z
  241297. GABRIEL WEATHERHEADy
  241298. Greenwic , CT
  241299. 19418
  241300. Schlosser, M.B
  241301. Organometallics. A ManualC
  241302. WileyM
  241303. 20427N
  241304. 2/28/96V
  241305. Titanium in Organic SynthesisW
  241306. 1994X
  241307. 195-282a
  241308. GABRIEL WEATHERHEADy
  241309. Chichester
  241310. 19419
  241311. Kreher, R. P.B
  241312. Heteroarenes II, Part 1K
  241313. Georg Thieme VerlagM
  241314. 20428N
  241315. 2/28/96V
  241316. Quinoline 1-OxidesW
  241317. 1991X
  241318. 493-541Y
  241319. GABRIEL WEATHERHEADy    Stuttgart
  241320. 19420
  241321. Kreher, R. P.B
  241322. Heteroarenes II, Part 1K
  241323. Georg Thieme VerlagM
  241324. 20429N
  241325. 2/28/96V
  241326. QuinolinesW
  241327. 1991X
  241328. 290-492Y
  241329. GABRIEL WEATHERHEADy    Stuttgart
  241330. 19421
  241331. Kreher, R. P.B
  241332. Heteroarenes II, Part 1K
  241333. Georg Thieme VerlagM
  241334. 20430N
  241335. 2/28/96
  241336. RV$1-A kyl- and 1-Arylquinolinium SaltsW
  241337. 1991X
  241338. 542-570Y
  241339. GABRIEL WEATHERHEADy    Stuttgart
  241340. 19422
  241341. Liotta, D.B
  241342. Organoselenium ChemistryK
  241343. WileyM
  241344. 20431N
  241345. 2/28/96V
  241346. Selenium-Stabilized CarbanionsW
  241347. 1987X
  241348. 243-276a
  241349. GABRIEL WEATHERHEADy
  241350. New York
  241351. 19423
  241352. Regitz, M.B
  241353. Organophosphorus Compounds IK
  241354. Georg Thieme VerlagM
  241355. 20432N
  241356. 2/28/96VMPhosphorus(III) Compounds with Coordination / Number  : Alkylidene PhosphanesW
  241357. 1982X
  241358. 23-25Y
  241359. GABRIEL WEATHERHEADy    Stuttgart
  241360. 19424
  241361. Regitz, M.B
  241362. Organophosphorus Compounds IK
  241363. Georg Thieme VerlagM
  241364. 20433N
  241365. 2/28/96V3Phosphorus(V) Compounds with Coordination /Number 3W
  241366. 1982X
  241367. 583-615Y
  241368. GABRIEL WEATHERHEADy    Stuttgart
  241369. 19425
  241370. Schaumann, E.B
  241371. Heteroarenes III, Part 4K
  241372. Georg Thieme VerlagM
  241373. 20434N
  241374. 2/28/96V11,3,4-Thiadiazoles, 1,3,4-Thiadiazolium CompoundsW
  241375. 1994X
  241376. 189-304Y
  241377. GABRIEL WEATHERHEADy    Stuttgart
  241378. 19426
  241379. Oae, S.B
  241380. Rev. Heteroatom Chem.C
  241381. MYU K.K.M
  241382. 20435
  241383. 2/28/96VaSynthesis and conformation of 2' -> 5' and 3' -> 5' phosphodiester linked branched triadenylates.W
  241384. 1988Z
  241385. GABRIEL WEATHERHEADy
  241386. Tokyo, Japan
  241387. 19427
  241388. German, L.//Zemskov, S.B(Organometallics in Organic Synthesis. 2.C
  241389. ORGANOMETALLICS /CHROMIUM CARBENOIDS /CYCLOADDITION /[2+1] /Cr /CHROMIUM  COMPLEXES /(CO)5 r=CPh(OMe) /C=C /ALKENES /CYCLOADDITION /[2+1] /CYCLOPROPANATION /CARBRING /3  /CYCLOPROPANEK
  241390. SpringerM
  241391. 20436N
  241392. 2/28/96VGDonor-Acceptor-Substituted Cyclopropanes via Fischer Carbene Complexes.W
  241393. 1989X
  241394. GABRIEL WEATHERHEADy
  241395. Berlin
  241396. 19428
  241397. YA!Suschitzky, H.//Scriven, E. F. V.B"Progress in Heterocyclic ChemistryC%FUNCTIONAL GROUPS /BIOTRANSFORMATIONSK
  241398. Pergamon PressM
  241399. 20437N
  241400. 2/28/96V6Biotransformations Relating to Heterocyclic Compounds.W
  241401. 1989Z
  241402. GABRIEL WEATHERHEADy
  241403. Oxford, U.K.
  241404. 19429
  241405. Trost, B. M.//Fleming, I.B
  241406. Comprehensive Organic SynthesisC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[M+N]
  241407. Pergamon PressM
  241408. 20438N
  241409. 2/28/96V
  241410. [4+4] and [6+4] Cycloadditions.W
  241411. 1991X
  241412. GABRIEL WEATHERHEADy
  241413. Oxford
  241414. 19430
  241415. Trost, B. M.//Fleming, I.B
  241416. Comprehensive Organic SynthesisC PHYSICAL ORGANIC /REARRANGEMENTSK
  241417. Pergamon PressM
  241418. 20439N
  241419. 2/28/96V
  241420. The Pinacol Rearrangement.W
  241421. 1991X
  241422.  721Z
  241423. GABRIEL WEATHERHEADy
  241424. Oxford
  241425. 19431
  241426. Trost, B. M.//Fleming, I.B
  241427. Comprehensive Organic SynthesisC PHYSICAL ORGANIC /REARRANGEMENTSK
  241428. Pergamon PressM
  241429. 20440N
  241430. 2/28/96V)Acid-catalyzed Rearrangement of Epoxides.W
  241431. 1991X
  241432. GABRIEL WEATHERHEADy
  241433. Oxford
  241434. 19432
  241435. Thumme , R. P.B#Adv. Theoretically Interesting Mol.C7C-C BOND FORMATION /AROMATICS /HETEROAROMATIC SYNTHESISK
  241436. Jai Press, Inc.M
  241437. 20441N
  241438. 2/28/96V
  241439. Isobenzofurans.W
  241440. 1989Z
  241441. GABRIEL WEATHERHEADy
  241442. Greenwich, CT
  241443. 19433
  241444. Creary, X.B
  241445. Adv. Carbocation ChemistryK
  241446. Jai Press, Inc.M
  241447. 20442N
  241448. 2/28/96
  241449. ^VwSimple Relationships Between Carbocation Lifetime and the Mechanism for Nucleophilic  Substitution at Saturated Carbon.W
  241450. 1989Z
  241451. GABRIEL WEATHERHEADy
  241452. Greenwich, CT
  241453. 19434
  241454. ApSimon, .B(The Total Synthesis of Natural Products.C2TARGET SYNTHESIS /LEUKOTRIENES /C-C BOND FORMATIONK
  241455. WileyM
  241456. 20443N
  241457. 2/28/96V
  241458. Synthesis of the Leukotrienes.W
  241459. 1988X
  241460. GABRIEL WEATHERHEADy
  241461. New York
  241462. 19435
  241463. Trost, B. M.//Fleming, I.B
  241464. Comprehensive Organic SynthesisC(C-C BOND FORMATION /APPENDAGES /COUPLINGK
  241465. Pergamon PressM
  241466. 20444N
  241467. 2/28/96V
  241468. Pinacol Coupling Reactions.W
  241469. 1991X
  241470. GABRIEL WEATHERHEADy
  241471. Oxford
  241472. 19436
  241473. Trost, B. M.//Fleming, I.B
  241474. Comprehensive Organic SynthesisC6C-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITIONK
  241475. Pergamon PressM
  241476. 20445N
  241477. 2/28/96V The Henry (Nitroaldol) Reaction.W
  241478. 1991X
  241479. GABRIEL WEATHERHEADy
  241480. Oxford
  241481. 19437
  241482. Atta-ur-rahman//Basha, F. Z.
  241483. bBOStudies in Natural Products Chemistry, Vol 13 : Bioactive Natural Products Pt AK
  241484. ElsevierM
  241485. 20446N
  241486. 2/28/96V5Naturally Occurring Mevinic Acids - Synthetic StudiesW
  241487. 1993X
  241488. 553-627a
  241489. GABRIEL WEATHERHEADy
  241490. Amsterdam, Netherlands
  241491. 19438
  241492. Trost, B. M.//Fleming, I.B
  241493. Comprehensive Organic SynthesisC6C-C BOND FORMATION /APPENDAGES /EN LATES /1,2-ADDITIONK
  241494. Pergamon PressM
  241495. 20447N
  241496. 2/28/96V
  241497. The Perkin Reaction.W
  241498. 1991X
  241499. GABRIEL WEATHERHEADy
  241500. Oxford
  241501. 19439
  241502. Trost, B. M.//Fleming, I.B
  241503. Comprehensive Organic SynthesisC6C-C BOND FORMATION /APPENDAGES /ENOLATES /1,2-ADDITIONK
  241504. Pergamon PressM
  241505. 20448N
  241506. 2/28/96V$Darzens Glycidic Ester Condensation.W
  241507. 1991X
  241508. GABRIEL WEATHERHEADy
  241509. Oxford
  241510. 19440
  241511. Trost, B. M.//Fleming, I.B
  241512. Comprehensive Organic SynthesisC5C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /C=C-C-MK
  241513. Pergamon PressM
  241514. 20449N
  241515. 2/28/96V
  241516. Allyl Organometallics.W
  241517. 1991X
  241518. GABRIEL WEATHERHEADy
  241519. Oxford
  241520. 19441
  241521. Curran, D. P.
  241522.  dv. CycloadditionC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2]K
  241523. Jai Press, Inc.M
  241524. 20450N
  241525. 2/28/96VPStereochemical and Synthetic Studies of the Intramolecular Diels-Alder Reaction.W
  241526. 1990Z
  241527. GABRIEL WEATHERHEADy
  241528. Greenwich, CT
  241529. 19442
  241530. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.K
  241531. Academic PressM
  241532. 20451N
  241533. 2/28/96V
  241534. Evolution of a Strategy for the Synthesis of Olivomycin A: Development of Methodology for the  Diastereo- and Enantioselective Synthesis of Carbohydrates from Acyclic Precursors.W
  241535. 1988Z
  241536. GABRIEL WEATHERHEAD
  241537. 19443
  241538. Morrison, J. D.B
  241539. Asymmetric Synthesis.C
  241540. C-C BOND FORMATION /HETEROANNULATIONS /3-RING /ENANTIOGENIC REACTIONS  /STEREOCHEMISTRY /SHARPLESS ASYMMETRIC EPOXIDATION KINETIC RESOLUTION HETEROANNULAT ON /3-RING(O) /HETRING /3(O) /OXIRANES /EPOXIDESK
  241541. 20452N
  241542. 2/28/96V=Synthetic Aspects and Applications of Asymmetric Epoxidation.W
  241543. 1985X
  241544. GABRIEL WEATHERHEADy
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  241546. 19444
  241547. Tanner, D. D.B
  241548. Adv. Free Radical Chem.C>PHYSICAL ORGANIC /MECHANISMS /REACTI E INTERMEDIATES /RADICALSK
  241549. Jai Press, Inc.M
  241550. 20453N
  241551. 2/28/96VANucleophilic substitution by the SRN1 mechanism on alkyl halides.W
  241552. 1990Z
  241553. GABRIEL WEATHERHEADy
  241554. Greenwich, CT
  241555. 19445
  241556. Brossi, A.B
  241557. The Alkaloids. Chem. and Pharm.K
  241558. Academic PressM
  241559. 20454N
  241560. 2/28/96V
  241561. Benzodiazepine alkaloids.W
  241562. 1990Z
  241563. GABRIEL WEATHERHEADy
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  241565. 19446
  241566. Cadogan, J. I. G.B/Organophosphorus Reagents in Organic Synthesis.C
  241567. FUNCTIONAL GROUPS /TRANSFORMATIONS /DEOXYGENATION /ESTERIFICATION DEHYDRATION  /C=C /ALKYNES /HETRING /3(O) /OXIRANES /EPOXIDES /C=C /ALKENES /PK
  241568. 20455N
  241569. 2/28/96VXDeoxygenations using Phosphorus (III) Reagents. 2. General Functional Group Conversions.W
  241570. 1979X
  241571. GABRIEL WEATHERHEADy
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  241573. 19447
  241574. Trost, B. M.//F eming, I.B
  241575. Comprehensive Organic SynthesisC?C-C BOND FORMATION /PERICYCLIC REACTIONS /CYCLOADDITIONS /[4+2]K
  241576. Pergamon PressM
  241577. 20456N
  241578. 2/28/96
  241579. lV%Intramolecular Diels-Alder Reactions.W
  241580. 1991X
  241581. GABRIEL WEATHERHEADy
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  241583. 19448
  241584. Tanner, D. D.B
  241585. Adv. Free Radical Chem.CPORGANOMETALLICS /MERCURY /PHYSICAL ORGANIC /REACTIVE INTERMEDIATES /RADICALS /HgK
  241586. Jai Press, Inc.M
  241587. 20457N
  241588. 2/28/96VKFree radical reactions involving saturated and unsaturated alkylmercurials.W
  241589. 1990Z
  241590. GABRIEL WEATHERHEADy
  241591. Greenwich, CT
  241592. 19449
  241593. Kreher, R. P.B
  241594. Heteroarenes I, Part 1K
  241595. Georg Thieme VerlagM
  241596. 20458N
  241597. 2/28/96V
  241598. ThiophenesW
  241599. 1994X
  241600. 186-555Y
  241601. GABRIEL WEATHERHEADy    Stuttgart
  241602. 19450
  241603. Kr her, R. P.B
  241604. Heteroarenes II, Part 2K
  241605. Georg Thieme VerlagM
  241606. 20459N
  241607. 2/28/96V
  241608. Dibenzo[b /d]thiopyrylium SaltsW
  241609. 1992X
  241610. 103-114Y
  241611. GABRIEL WEATHERHEADy    Stuttgart
  241612. 19451
  241613. Kreher, R. P.B
  241614. Heteroarenes II, Part 1K
  241615. Georg Thieme VerlagM
  241616. 20460N
  241617. 2/28/96V
  241618. 3-Benzothiopyrylium SaltsW
  241619. 1991X
  241620. 266-289Y
  241621. GABRIEL WEATHERHEADy    Stuttgart
  241622. 19452
  241623. Trost, B. M.//Fleming, I.
  241624. Comprehensive Organic SynthesisC
  241625. ORGANOMETALLICS /CHROMIUM /CrK
  241626. Pergamon PressM
  241627. 20461N
  241628. 2/28/96V
  241629. Organochromium Reagents.W
  241630. 1991X
  241631. GABRIEL WEATHERHEADy
  241632. Oxford
  241633. 19453
  241634. Kropf, H.//Schaumann, E.B
  241635. Ene,X and Yne,X-CompoundsK
  241636. Georg Thieme VerlagM
  241637. 20462N
  241638. 2/28/96V)Heterosubstituted Allenes and PolyallenesW
  241639. 1993X    2959-3118Y
  241640. GABRIEL WEATHERHEADy    Stuttgart
  241641. 19454
  241642. Hanack, M.B
  241643. CarbanionsK
  241644. Georg Thieme VerlagM
  241645. 20463N
  241646. 2/28/96V!Acyl Anions and their DerivativesW
  241647. 1993X
  241648. 567-712Y
  241649. E19da
  241650. GABRIEL WEATHERHEADy    Stuttgart
  241651. 19455
  241652. Dondoni, A.B5Advances in the Use of Synthons in Organic Chemistr .K    Jai PressM
  241653. 20464N
  241654. 2/28/96VeFrom push-pull-substituted allenes to tetra-nuclear chelate complexes via spontaneous  self-assembly.W
  241655. 1993Z
  241656. GABRIEL WEATHERHEADy
  241657. Greenwich, CT
  241658. 19456
  241659. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic Chemistry
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  241661. Pergamon PressM
  241662. 20465N
  241663. 2/28/96V7Triazoles and Tetrazoles with Fused Six-membered Rings.W
  241664. 1984X
  241665. GABRIEL WEATHERHEADy
  241666. Oxford
  241667. 19457
  241668. Oae, S.B Reviews on Heteroatom Chemistry.C
  241669. MYU K.K.M
  241670. 20466N
  241671. 2/28/96VTCatalytic synthesis of thiophene and alkylthiophenes via heterocyclization reaction.W
  241672. 1994Z
  241673. GABRIEL WEATHERHEADy
  241674. Tokyo, Japan
  241675. 19458
  241676. Trost, B. M.//Fleming, I.B
  241677. Comprehensive Organic SynthesisC
  241678. FUNCTIONAL GROUPS /REDUCTIONK
  241679. Pergamon PressM
  241680. 20467N
  241681. 2/28/96VSPartial  nd Complete Reduction of Heterocycles Containing More than One Heteroatom.W
  241682. GABRIEL WEATHERHEADy
  241683. Oxford
  241684. 19459
  241685. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC
  241686. OXAZINONES /THIAZINONESK
  241687. Pergamon PressM
  241688. 20468N
  241689. 2/28/96V0Oxazines, Thiazines and their Benzo Derivatives.W
  241690. 1984X
  241691. GABRIEL WEATHERHEADy
  241692. Oxford
  241693. 19460
  241694. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryK
  241695. Pergamon Press  OxfordM
  241696. 20469N
  241697. 2/28/96V)Dioxazoles, Oxathiazoles and Dithiazoles.W
  241698. 1984X
  241699. GABRIEL WEATHERHEAD
  241700. 19461
  241701. Werner, H.//Erker, G.B(Organometallics in  rganic Synthesis. 2.C>ORGANOMETALLICS /Fe /DIOLEFIN IRON COMPLEXES /(C=C-C=C)Fe(CO)3K
  241702. Springer-VerlagM
  241703. 20470N
  241704. 2/28/96VJDiolefin Iron Complexes - Useful and Versatile Tools in Organic Synthesis.W
  241705. 1989X
  241706. GABRIEL WEATHERHEADy
  241707. Berlin
  241708. 19462
  241709. Mayo, P. D.B,Rearrangements in Gr und and Excited States.CnPHYSICAL ORGANIC /REARRANGEMENTS /PHOTOCHEMICAL REACTIONS /C=C /ALKENE(Z)  /ISOMERIZATION(Z-E) /C=C /ALKENE(E)K
  241710. 20471N
  241711. 2/28/96V#Cis Trans Isomerisation of Alkenes.W
  241712. 1980X
  241713. GABRIEL WEATHERHEADy
  241714. New York
  241715. 19463
  241716. Lindbe g, T.B+Strategies and Tactics in Organic SynthesisK
  241717. Academic PressM
  241718. 20472N
  241719. 2/28/96V8Synthesis of a Cancer Growth-inhibiting Diterpene SpatolW
  241720. 1991X
  241721. 382-417Z
  241722. GABRIEL WEATHERHEADy
  241723. San Diego, CA
  241724. 19464
  241725. Hartley, F. R.B8The Use of Organometallic Compound Organi  in Synthesis.C
  241726. WileyM
  241727. 20473N
  241728. 2/28/96VZPreparation and Use of Grignard Reagents and Group II Organometallics in Organic SynthesisW
  241729. 1987X
  241730. 159-306Z
  241731. GABRIEL WEATHERHEADy
  241732. Chichester
  241733. 19465
  241734. ~A    Kropf, H.B
  241735. Carbocyclic pi-Electron SystemsK
  241736. Georg Thieme VerlagM
  241737. 20474N
  241738. 2/28/96V
  241739. Cyclooctatetraene DianionsW
  241740. 19 5X
  241741. 86-93Y
  241742. 5/2ca
  241743. GABRIEL WEATHERHEADy    Stuttgart
  241744. 19466
  241745. Oae, S.B
  241746. Rev. Heteroatom Chem.C
  241747. MYU K.K.M
  241748. 20475N
  241749. 2/28/96V=Organic synthesis with sulfinyloxiranes and sulfonyloxiranes.W
  241750. 1992Z
  241751. GABRIEL WEATHERHEADy
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  241753. 19467
  241754. Oae, S.B
  241755. Rev. Heteroatom Chem.C
  241756. MYU K.K.M
  241757. 20476N
  241758. 2/28/96V=Reactions of elemental sulfur activated by ammonia or amines.W
  241759. 1990Z
  241760. GABRIEL WEATHERHEADy
  241761. Tokyo, Japan
  241762. 19468
  241763. Hiraoka, M.B$Crown Ethers and Analogous CompoundsK
  241764. Elsevier Science Publ B VM
  241765. 20477N
  241766. 2/28/96V"Enzyme Modelling with Crown EthersW
  241767. 1992X
  241768. 265-310a
  241769. GABRIEL WEATHERHEADy
  241770. Amsterdam, Netherlands
  241771. 19469
  241772. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC
  241773. BENZOFURANES /FURANONESK
  241774. Pergamon PressM
  241775. 20478N
  241776. 2/28/96V4Furans and their Benzo Derivatives: (ii) Reactivity.W
  241777. 1984X
  241778. GABRIEL WEATHERHEADy
  241779. Oxford
  241780. 19470
  241781. A    Padwa, A.B
  241782. Org. Photochem.K
  241783. DekkerM
  241784. 20479N
  241785. 2/28/96V)Photochemistry of reaction intermediates.W
  241786. 1989Z
  241787. GABRIEL WEATHERHEADy
  241788. New York
  241789. 19471
  241790. Ando, W.B
  241791. Organic PeroxidesK
  241792. WileyM
  241793. 20480N
  241794. 2/28/96V
  241795. Peroxy Acids and Peroxy EstersW
  241796. 1992X
  241797. 425-477a
  241798. GABRIEL WEATHERHEADy
  241799. Chichester, U. K.
  241800. 19472
  241801. Oae, S.
  241802. Rev. Heteroatom Chem.C
  241803. FK    MYU K. K.M
  241804. 20481N
  241805. 2/28/96VNFluorinated organic peroxides - their decomposition behavior and applications.W
  241806. 1993Z
  241807. GABRIEL WEATHERHEADy
  241808. Tokyo, Japan
  241809. 19473
  241810. Kreher, R. P.B
  241811. Heteroarenes I, Part 1K
  241812. G org Thieme VerlagM
  241813. 20482N
  241814. 2/28/96V
  241815. DibenzothiophenesW
  241816. 1994X
  241817. 867-921Y
  241818. GABRIEL WEATHERHEADy    Stuttgart
  241819. 19474
  241820. Mayo, P. D.B,Rearrang ments in Ground and Excited States.C.PHYSICAL ORGANIC /REARRANGEMENTS /CARBOCATIONSK
  241821. 20483N
  241822. 2/28/96V
  241823. Rearrangements of Carbocations.W
  241824. 1980X
  241825. GABRIEL WEATHERHEADy
  241826. New York
  241827. 19475
  241828. Bush, C. A.B(Advances in Biophysical Chemistry, Vol 3K
  241829. Jai Press IncM
  241830. 20484N
  241831. 2/28/96V*Geometric Requirements of Proton TransfersW
  241832. 1993X
  241833. 119-159a
  241834. GABRIEL WEATHERHEADy
  241835. Greenwich, CT
  241836. 19476
  241837. Kropf, H.//Schaumann, E.B
  241838. Ene,X and Yne,X-CompoundsK
  241839. Georg Thieme VerlagM
  241840. 20485N
  241841. 2/28/96V
  241842. KetenesW
  241843. 1993X    2353- 530Y
  241844. GABRIEL WEATHERHEADy    Stuttgart
  241845. 19477
  241846. Kropf, H.//Schaumann, E.B
  241847. Ene,X and Yne,X-CompoundsK
  241848. Georg Thieme VerlagM
  241849. 20486N
  241850. 2/28/96V:Diheterosubstituted Ketenes, Thioketenes, Ketenimines etc.W
  241851. 1993X    2933-2958Y
  241852. GABRIEL WEATHERHEADy    Stuttgart
  241853. 19478
  241854. Kropf, H.//Schaumann, E.B
  241855. Ene,X and Yne,X-CompoundsK
  241856. Georg Thieme VerlagM
  241857. 20487N
  241858. 2/28/96V<Monoheterosubstituted Ketenes, Thioketenes, Ketenimines etc.W
  241859. 1993X    281 -2881Y
  241860. GABRIEL WEATHERHEADy    Stuttgart
  241861. 19479
  241862. Trost, B. M.//Fleming, I.B
  241863. Comprehensive Organic SynthesisC;FUNCTIONAL GROUPS /PREPARATIONS /ORGANOSULPHUR COMPOUNDS /SK
  241864. Pergamon PressM
  241865. 20488N
  241866. 2/28/96V(Synthesis of Thioamides and Thiolactams.W
  241867. 1991X
  241868. GABRIEL WEATHERHEADy
  241869. Oxford
  241870. 19480
  241871. Klamann, D.B
  241872. Organosulfur CompoundsK
  241873. Georg Thieme VerlagM
  241874. 20489N
  241875. 2/28/96V!Thioketenes and Their DerivativesW
  241876. 1985X
  241877. 232-341Y
  241878. GABRIEL WEATHERHEADy    Stuttgart
  241879. 19481
  241880. Klamann, D.B
  241881. Organosulfur CompoundsK
  241882. Georg Thieme VerlagM
  241883. 20490N
  241884. 2/28/96
  241885. Sulfones and Their DerivativesW
  241886. 1985X    1129-1326Y
  241887. GABRIEL WEATHERHEADy    Stuttgart
  241888. 19482
  241889. Mayo, P. D.B,Rearrangements in Ground and Excited States.CcPHYSICAL ORGANIC /REARRANGEMENTS /PHOTOCHEMICAL REACTIONS /O=C-C=C-C=C  /CONJUGATED CYCLIC DIENONESK
  241890. 20491N
  241891. 2/28/96V;Photochemical Rearrangements of Conjugated Cyclic Dienones.W
  241892. 1980X
  241893. GABRIEL WEATHERHEADy
  241894. New York
  241895. 19483
  241896. Coxon, J. M.B(Advances in Detailed Reaction MechanismsK
  241897. Jai Press IncM
  241898. 20492N
  241899. 2/28/96V'Recent Advances in Catalytic AntibodiesW
  241900. 1992X
  241901. 1-22Z
  241902. GABRIEL WEATHERHEADy
  241903. Greenwich, CT
  241904. 19484
  241905. Schlosser, M.B
  241906. Organometallics. A ManualC    Li /K /NaK
  241907. WileyM
  241908. 20493N
  241909. 2/28/96V
  241910. Organoalkali ReagentsW
  241911. 1994X
  241912. 1-166a
  241913. GABRIEL WEATHERHEADy
  241914. Chichester
  241915. 19485
  241916. Scheffold, R.B
  241917. Modern Synthetic MethodsK
  241918. Verlag Helvetica Chimica ActaM
  241919. 20494N
  241920. 2/28/96V1Superbases as Powerful Tools in Organic SynthesesW
  241921. 1992X
  241922. 227-271Z
  241923. GABRIEL WEATHERHEADy
  241924. Basel, Switzerland
  241925. 19486
  241926. Werner, H.//Erker, G.B(Organometal ics in Organic Synthesis. 2.CRORGANOMETALLICS /C-M /Cr /Ar-M /Cr /ArCr(CO)3 /ARENETRICARBONYLCHROMIUM  COMPLEXESK
  241927. SpringerM
  241928. 20495N
  241929. 2/28/96VjStereochemistry of Arenetricarbonylchromium Complexes Useful Intermediates for  Stereoselective Syntheses.W
  241930. 1989X
  241931. GABRIEL WEATHERHEADy
  241932. Berlin
  241933. 19487
  241934. Trost, B. M.//Fleming, I.B
  241935. Comprehensive Organic SynthesisC+FUNCTIONAL GROUPS /OXIDATION /MISCELLANEOUSK
  241936. Pergamon PressM
  241937. 20496N
  241938. 2/28/96V"Oxidative Rearrangement Reactions.W
  241939. 1991X
  241940. GABRIEL WEATHERHEADy
  241941. Oxford
  241942. 19488
  241943. Klamann, D.B
  241944. Organosulfur CompoundsK
  241945. Georg Thieme VerlagM
  241946. 20497N
  241947. 2/28/96V$Sulfonic Acids and Their DerivativesW
  241948. 1985X    1042-1128Y
  241949. GABRIEL WEATHERHEADy    Stuttgart
  241950. 19489
  241951. 20498N
  241952. 2/28/96V
  241953. Kolbe Reactions.W
  241954. 1991a
  241955. GABRIEL WEATHERHEAD
  241956. 19490
  241957. 20499N
  241958. 2/28/96W
  241959. 1992a
  241960. GABRIEL WEATHERHEAD
  241961. 19491
  241962. Katritzky, A. R.//Rees, C. W.
  241963. B$Comprehensive Heterocyclic ChemistryCHOXAZIRIDINES /DIAZIRIDINES /DIAZIRIDINONES /DIAZIRIDINIMINES /DIAZIRINESK
  241964. Pergamon PressM
  241965. 20500N
  241966. 2/28/96VEThree-membered Rings with Two Heteroatoms and Fused-ring Derivatives.W
  241967. 1984X
  241968. GABRIEL WEATHERHEADy
  241969. Oxford
  241970. 19492
  241971. A    Falbe, J.B7Organo-pi-metal Compounds as Acids in Organic ChemistryK
  241972. Georg Thieme VerlagM
  241973. 20501N
  241974. 2/28/96V(Catalytic Reactions: Oxidative ReactionsW
  241975. 1986X    1077-1136Y
  241976. GABRIEL WEATHERHEADy    Stuttgart
  241977. 19493
  241978. A"Ogura, H.//Hasega a, A.//Suami, T.B
  241979. CarbohydratesK
  241980. Kodansha LtdM
  241981. 20502N
  241982. 2/28/96V&New Aspects of Glycosylation ReactionsW
  241983. 1992X
  241984. 66-88a
  241985. GABRIEL WEATHERHEADy
  241986. Tokyo, Japan
  241987. 19494
  241988. Trost, B. M.//Fleming, I.B
  241989. Comprehensive Organic SynthesisC1FUNCTIONAL GROUPS /TRANSFORMATIONS /CARBOHYDRATESK
  241990. Pergamon PressM
  241991. 20503N
  241992. 2/28/96V
  241993. Synthesis of Glycosides.W
  241994. 1991X
  241995. GABRIEL WEATHERHEADy
  241996. Oxford
  241997. 19495
  241998. K ster, R.B
  241999. Organoboron Compounds III
  242000. Georg Thieme VerlagM
  242001. 20504N
  242002. 2/28/96VBOrganoboron Compounds with Four-to Sixfold Coordinated Boron AtomsW
  242003. 1984X
  242004. 1-214Y
  242005. 13/3ca
  242006. GABRIEL WEATHERHEADy    Stuttgart
  242007. 19496
  242008. Trost, B. M.//Fleming, I.B
  242009. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APP NDAGES /1,4-ADDITIONK
  242010. Pergamon PressM
  242011. 20505N
  242012. 2/28/96V?Asymmetric Nucleophilic Addition to Electron Deficient Alkenes.W
  242013. 1991X
  242014. GABRIEL WEATHERHEADy
  242015. Oxford
  242016. 19497
  242017. Schaumann, E.B
  242018. Heteroarenes III, Part 2K
  242019. Georg Thieme VerlagM
  242020. 20506N
  242021. 2/28/96V
  242022. 1,3-BenzothiazolesW
  242023. 1994X
  242024. 865-1062Y
  242025. GABRIEL WEATHERHEADy    Stuttgart
  242026. 19498
  242027. 20507N
  242028. 2/28/96W
  242029. 1985a
  242030. GABRIEL WEATHERHEAD
  242031. 19499
  242032. Kreher, R. P.B
  242033. Hetarenes II, Part IIK
  242034. Georg Thieme VerlagM
  242035. 20508N
  242036. 2/28/96V
  242037. Pyrylium SaltsW
  242038. 1992X
  242039. 755-1004Y
  242040. GABRIEL WEATHERHEADy    Stuttgart
  242041. 19500
  242042. Trost, B. M.//Fleming, I.B
  242043. Comprehensive Organic SynthesisC&C-C BOND FORM TION /ANNULATION /6-RINGK
  242044. Pergamon Press
  242045. 20509N
  242046. 2/28/96V
  242047. [2+2+2] Cycloadditions.W
  242048. 1991X
  242049. 1129Z
  242050. GABRIEL WEATHERHEADy
  242051. Oxford
  242052. 19501
  242053. Trost, B. M.//Fleming, I.B
  242054. Comprehensive Organic SynthesisC6C-C BOND FORMATION /ANNULATION /5-RING /CYCLOPENTENONEK
  242055. Pergamon PressM
  242056. 20510N
  242057. 2/28/96V
  242058. The Pauson-Khand Reactions.W
  242059. 1991X
  242060. 1037Z
  242061. GABRIEL WEATHERHEADy
  242062. Oxford
  242063. 19502
  242064. Regitz, M.B
  242065. Carbenes (Carbenoids)K
  242066. Georg Thieme VerlagM
  242067. 20511N
  242068. 2/28/96V#Carbenes (Carbenoids): IntroductionW
  242069. 1989X
  242070. 1-57Y
  242071. E19ba
  242072. GABRIEL WEATHERHEADy    Stuttgart
  242073. 19503
  242074. A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid DerivativesK
  242075. Georg Thieme VerlagM
  242076. 20512N
  242077. 2/28/96V
  242078. AmidinesW
  242079. 1985X    1304-1312Y
  242080. GABRIEL WEATHERHEADy    Stuttgart
  242081. 19504
  242082. Schaumann, E.B
  242083. Heteroarenes III, Part 1K
  242084. Georg Thieme VerlagM
  242085. 20513N
  242086. 2/28/96V
  242087. 1,2-ThiazolesW
  242088. 1993X
  242089. 668-798Y
  242090. GABRIEL WEATHERHEADy    Stuttgart
  242091. 19505
  242092. Schaumann, E.B
  242093. Heteroarenes III, Part 1K
  242094. Georg Thieme VerlagM
  242095. 20514N
  242096. 2/28/96
  242097. 1,2-BenzothiazolesW
  242098. 1993X
  242099. 799-852Y
  242100. GABRIEL WEATHERHEADy    Stuttgart
  242101. 19506
  242102. Schaumann, E.B
  242103. Heteroarenes III, Part 1K
  242104. Georg Thieme VerlagM
  242105. 20515N
  242106. 2/28/96V
  242107. 2,1-BenzothiazolesW
  242108. 1993Z
  242109. GABRIEL WEATHERHEADy    Stuttgart
  242110. 19507
  242111. Bartl, H.//Falbe, J.B
  242112. Macromolecular MaterialsK
  242113. Georg Thieme VerlagM
  242114. 20516N
  242115. 2/28/96V1Polymers with C- and Heteroatom in the Main ChainW
  242116. 1987Z
  242117. GABRIEL WEATHERHEADy    Stuttgart
  242118. 19508
  242119. Bartl, H.//Falbe, J.B
  242120. Macromolecular MaterialsK
  242121. Georg Thieme VerlagM
  242122. 20517N
  242123. 2/28/96VxPreparation of Macromol ular Materials by Reactions at Macromolecules (General Chemical Reactions, Graft Polymerization)W
  242124. 1987X
  242125. 608-625Y
  242126. GABRIEL WEATHERHEADy    Stuttgart
  242127. 19509
  242128. Curran, D. P.B
  242129. Adv. CycloadditionK
  242130. Jai Press, Inc.M
  242131. 20518N
  242132. 2/28/96V
  242133. Molecular Rearrangements Occurring from Products of Intramolecular 1,3 Dipolar Cycloadditions:  Synthetic and Mechanistic Aspects.W
  242134. 1988Z
  242135. GABRIEL WEATHERHEAD
  242136. Greenwich, CT
  242137. 19510
  242138. Morrison, J. D.//Scott, J. W.B
  242139. Asymmetric SynthesisCeC-C BOND FORMATION /USEFUL FRAGMENTS /APPENDAGES /DIASTEREOGENIC REACTIONS  /STEREOCHEMI TRY /CHIRONSK
  242140. 20519N
  242141. 2/28/96VEReadily Available Chiral Carbon Fragments and Their Use in Synthesis.W
  242142. 1984X
  242143. GABRIEL WEATHERHEADy
  242144. New York
  242145. 19511
  242146. Marino, P. S.B'Advances in Electron Transfer ChemistryK    Jai PressM
  242147. 20520N
  242148. 2/28/96V
  242149. Electron Transfer Reactions Followed by Rapid Bond Cleavage: Intra-Ion Pair Electron Transfer  Photoexcited Cyanine Borates and Chemically Initiated Electron-Exchange Luminescence.W
  242150. 1991Z
  242151. GABRIEL WEATHERHEADy
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  242153. 19512
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  242155. 20521N
  242156. 2/28/96V'Photochemical Rearrangements of Enones.W
  242157. 1980X
  242158. GABRIEL WEATHERHEADy
  242159. New York
  242160. 19513
  242161. Scheff ld, R.B
  242162. Modern Synthetic Methods.
  242163. C,ORGANOMETALLICS /TITANIUM /ZIRCONIUM /Ti /ZrK
  242164. SpringerM
  242165. 20522N
  242166. 2/28/96V8Titanium and Zirconium Derivatives in Organic Synthesis.W
  242167. 1983X
  242168. GABRIEL WEATHERHEADy
  242169. Berlin
  242170. 19514
  242171. S heffold, R.B
  242172. Modern Synthetic Methods.K
  242173. Otto Salle VerlagM
  242174. 20523N
  242175. 2/28/96V
  242176. Syntheses of Enantiomerically Pure Compound (EPC - Syntheses). Tartaric Acid, an Ideal Source of  Chiral Building Blocks for Syntheses?W
  242177. 1980X
  242178. 91-171Z
  242179. GABRIEL WEATHERHEADy
  242180. Frankfurt/Main
  242181. 19515
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  242184. Pergamon  ressM
  242185. 20524N
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  242187. Oxetanes and Oxetenes.W
  242188. 1984X
  242189. GABRIEL WEATHERHEADy
  242190. Oxford
  242191. 19516
  242192. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic C emistryC:PYRIDINIUM CATIONS /PYRIDINONES /QUINOLINES /QUINOLINONES K
  242193. Pergamon PressM
  242194. 20525N
  242195. 2/28/96VEPyridines and their Benzo Derivatives: (ii) Reactivity at Ring Atoms.W
  242196. 1984X
  242197. GABRIEL WEATHERHEADy
  242198. Oxford
  242199. 19517
  242200. Segnitz, AB/Organometallic Compounds Mn, Re, Fe, Ru, Os, PtM
  242201. 20526N
  242202. 2/28/96V
  242203. sigma-Organoruthenium CompoundsW
  242204. 1986a
  242205. GABRIEL WEATHERHEAD
  242206. 19518
  242207. Segnitz, A.B/Organometallic Compounds Mn, Re, Fe, Ru, Os, PtK
  242208. Georg Thieme VerlagM
  242209. 20527N
  242210. 2/28/96V
  242211. sigma-Organoiron CompoundsW
  242212. 1986X
  242213. 176-523Y
  242214. 13/9aa
  242215. GABRIEL WEATHERHEADy    Stuttgart
  242216. 19519
  242217. Segnitz, A.B/Organometallic Compounds  n, Re, Fe, Ru, Os, PtK
  242218. Georg Thieme VerlagM
  242219. 20528N
  242220. 2/28/96V
  242221. sigma-Organoosmium CompoundsW
  242222. 1986X
  242223. 614-669Y
  242224. 13/9aa
  242225. GABRIEL WEATHERHEADy    Stuttgart
  242226. 19520
  242227. Segnitz, A.B/Organometallic Compounds Mn, Re, Fe, Ru, Os, PtK
  242228. Georg Thieme VerlagM
  242229. 20529N
  242230. 2/28/96V
  242231. sigma-Organomanganese CompoundsW
  242232. 1986X
  242233. 1-119Y
  242234. 13/9aa
  242235. GABRIEL WEATHERHEADy    Stuttgart
  242236. 19521
  242237. Segnitz, A.B/Organometallic Compounds Mn, Re, Fe, Ru, Os, PtK
  242238. Georg Thieme VerlagM
  242239. 20530N
  242240. 2/28/96V
  242241. sigma-Organorhenium Co poundsW
  242242. 1986X
  242243. 122-173Y
  242244. 13/9aa
  242245. GABRIEL WEATHERHEADy    Stuttgart
  242246. 19522
  242247. Segnitz, A.B+Organometallic Compounds Co, Rh, Ir, Ni, PdK
  242248. Georg Thieme VerlagM
  242249. 20531N
  242250. 2/28/96V
  242251. sigma-Organopalladium CompoundsW
  242252. 1984X
  242253. 702-999Y
  242254. 13/9ba
  242255. GABRIEL WEATHERHEADy    Stuttgart
  242256. 19523
  242257. Scheffold, R.B
  242258. Modern Synthetic Methods.C\C-C BOND FORMATION /APPENDAGES /ENANTIOGENIC REACTIONS /ACETALS /ENAMINES  /ENANTIOSELECTIVEK
  242259. SpringerM
  242260. 20532N
  242261. 2/28/96VZEnantiomerically Pure Compound Syntheses with C,C Bond Formation via Acetals and Enamines.W
  242262. 1986X
  242263. GABRIEL WEATHERHEADy
  242264. Berlin
  242265. 19524
  242266. Trost, B. M.//Fleming, I.B
  242267. Comprehensive Organic SynthesisC.C-C BOND FORMATION /AROMATICS /CHAIN APPENDAGEK
  242268. Perg mon PressM
  242269. 20533N
  242270. 2/28/96V/Nucleophilic Addition to Arene-Metal Complexes.W
  242271. 1991X
  242272. GABRIEL WEATHERHEADy
  242273. Oxford
  242274. 19525
  242275. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.K
  242276. Academic PressM
  242277. 20534N
  242278. 2/28/96V(The Synthesis of Fomannosin and Illudol.W
  242279. 1984Z
  242280. GABRIEL WEATHERHEAD
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  242284. Pergamo  PressM
  242285. 20535N
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  242287. Purines.W
  242288. 1984X
  242289. GABRIEL WEATHERHEADy
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  242291. 19527
  242292. Suschitzky, H.//Scriven, E. F.B"Progress in Heterocyclic ChemistryK
  242293. Pergamon PressM
  242294. 20536N
  242295. 2/28/96V
  242296. 2-Isoxazolines.W
  242297. 1992Z
  242298. GABRIEL WEATHERHEADy
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  242300. 19528
  242301. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryC
  242302. DIAZEPINES /DIOXEPINS /DITHIEPINS /OXAZEPINES /THIAZEPINES /TRIAZEPINES  /OXADIAZEPINES /THIADIAZEPINES /TETRAZEPINES /TETRATHIEPINS /OXATRIAZEPINES  /THIATRIAZEPINES /OXATHIADIAZEPINES /DITHIADIAZEPINES /DIOXATHIAZEPINES /DIOXADITHIEPINSK
  242303. Pergamon PressM
  242304. 20537N
  242305. 2/28/96V2Seven-membered Rings with Two or More Heteroatoms.W
  242306. 1984X
  242307. GABRIEL WEATHERHEADy
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  242309. 19529
  242310. Trost, B. M.//Fleming, I.
  242311. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APPENDAG S /1,2-ADDITIONK
  242312. Pergamon PressM
  242313. 20538N
  242314. 2/28/96V!Lewis Acid Carbonyl Complexation.W
  242315. 1991X
  242316. GABRIEL WEATHERHEADy
  242317. Oxford
  242318. 19530
  242319. A"Ma yanoff, B. E.//Maryanoff, C. A.B
  242320. Advances in Medicinal ChemistryK    Jai PressM
  242321. 20539N
  242322. 2/28/96V9Chemistry and Biology of the Immunosuppressant (-)-FK-506W
  242323. 1992X
  242324. 55-108Z
  242325. GABRIEL WEATHERHEADy    Greenwich
  242326. 19531
  242327. A    Dugas, H.B
  242328. Bioorganic Chemistry FrontiersK
  242329. SpringerM
  242330. 20540N
  242331. 2/28/96VmFunctionalization of Crown Ethers and Calixarenes: New Applications as Ligands, Carriers and Host  Molecules.W
  242332. 1990Z
  242333. GABRIEL WEATHERHEADy
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  242335. 19532
  242336. Comprehensive Organic SynthesiM
  242337. 20541N
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  242339. Glycol-Cleavage Reactions.W
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  242341. GABRIEL WEATHERHEAD
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  242345. 20542N
  242346. 2/28/96V4Silicon effects in solvolysis and related reactions.W
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  242348. GABRIEL WEATHERHEADy
  242349. Oxford, U.K.
  242350. 19534
  242351. K ster, R.B
  242352. Organoboron Compounds IK
  242353. Georg Thieme VerlagM
  242354. 20543N
  242355. 2/28/96VgOrganoboron Compounds with Threefold Coordinated Boron Atom: Organoboron Sulfur and Selenium  CompoundsW
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  242359. GABRIEL WEATHERHEADy    Stuttgart
  242360. 19535
  242361. Trost, B. M.//Fleming, I.B
  242362. Comprehensive Organic SynthesisC-FUNCTIONAL GROUPS /OXIDATION /ELECTROCHEMICALK
  242363. Pergamon  ressM
  242364. 20544N
  242365. 2/28/96V%Oxidation by Electrochemical Methods.W
  242366. 1991X
  242367. GABRIEL WEATHERHEADy
  242368. Oxford
  242369. 19536
  242370. Trost, B. M.//Fleming, I.B
  242371. Comprehensive Organic SynthesisC2FUNCTIONAL GROUPS /TRANSFORMATIO S /O=C-X TO O=C-YK
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  242373. 20545N
  242374. 2/28/96V#The Eschenmoser Coupling Reactions.W
  242375. 1991X
  242376. GABRIEL WEATHERHEADy
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  242378. 19537
  242379. Dondoni, A.B4Advances in the Use of Synthons in Organic ChemistryK
  242380. Jai Press IncM
  242381. 20546N
  242382. 2/28/96VFTrimethylsilyldiazomethane - A Versatile Synthon for Organic SynthesisW
  242383. 51-1 1Z
  242384. GABRIEL WEATHERHEADy    Greenwich
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  242387. Comprehensive Organic SynthesisC"FUNCTIONAL GROUPS /TRANSFORMATIONSK
  242388. Pergamon PressM
  242389. 20547N
  242390. 2/28/96V
  242391. Degradation Reactions.W
  242392. 1991X
  242393. GABRIEL WEATHERHEADy
  242394. Oxford
  242395. 19539
  242396. Gokel, G. W.B%Advances in Supramolecular Chemistry.K    Jai PressM
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  242398. 2/28/96V-Calixarenes as the third supramolecular host.W
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  242400. GABRIEL WEATHERHEADy
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  242407. 2/28/96V5Chemistry of Trialkylsilyl Perfluoralkane Sulfonates.W
  242408. 1991Z
  242409. GABRIEL WEATHERHEADy
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  242411. 19541
  242412. A    Falbe, J.B0Carboxylic Acids and Carboxylic Acid DerivativesK
  242413. Georg Thieme VerlagM
  242414. 20550N
  242415. 2/28/96V Orthocarboxylic Acid DerivativesW
  242416. 1985Z
  242417. GABRIEL WEATHERHEADy    Stuttgart
  242418. 19542
  242419. Hanack, M.B%Carbocations and Carbocation RadicalsK
  242420. Georg Thieme VerlagM
  242421. 20551N
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  242423. V2Carbonium Ions (Penta and hexacoordinated cations)W
  242424. 1990X
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  242427. GABRIEL WEATHERHEADy    Stuttgart
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  242429. Trost, B. M.//Fleming, I.B
  242430. Comprehensive Organic SynthesisC5FUNCTIONAL GROUPS /REDUCTION /CATALYTIC HYDROGENATIONK
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  242432. 20552N
  242433. 2/28/96V: Heterogeneous Catalytic Hydrogenation of C=C and Alkynes.W
  242434. 1991X
  242435. GABRIEL WEATHERHEADy
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  242438. A1Liebman, J. F.//Greenberg, A.//Dolbier, W. R., JrB}Fluorine-Containing Molecules. Structure, Reactivity, Synthesis and Application (Molecular  Structure and Energetics, Vol. 8)C
  242439. VCH PublishersM
  242440. 20553N
  242441. 2/28/96VhThe Effect of Fluorine as a Substituent on Selected Properties of Neutral and Charged Aromatic  Systems.W
  242442. 1988a
  242443. GABRIEL WEATHERHEADy
  242444. New York
  242445. 19545
  242446. Schlosser, M.B
  242447. Organometallics. A ManualC
  242448. WileyM
  242449. 20554N
  242450. 2/28/96V
  242451. Organoboron ChemistryW
  242452. 1994X
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  242454. GABRIEL WEATHERHEADy
  242455. Chichester
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  242458. B)Advances in Detailed Reaction Mechanisms.C
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  242461. 2/28/96VM1,4-Addition reactions of organocuprates with alpha,beta-unsaturated ketones.W
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  242463. GABRIEL WEATHERHEADy
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  242466. Trost, B. M.//Fleming, I.B
  242467. Comprehensive Organic SynthesisC1FUNCTIONAL GROUPS /REDUCTION /B /HYDROMETALLATIONK
  242468. Pergamon PressM
  242469. 20556N
  242470. 2/28/96V!Hydroboration of C=C and Alkynes.W
  242471. 1991X
  242472. GABRIEL WEATHERHEADy
  242473. Oxford
  242474. 19548
  242475. Katritzky, A. R.//Rees, C. W.B$Comprehensive Heterocyclic ChemistryK
  242476. Pergamon PressM
  242477. 20557N
  242478. 2/28/96V(Porphyrins, Corrins and Phthalocyanines.W
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  242480. GABRIEL WEATHERHEADy
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  242482. 19549
  242483. Cadogan, J. I. G.B.Organophosphorus Reagents in Organic SynthesisCGORGANOMETALLICS /ELEMENT /PHOSPHORUS /C-M(X) /Li(PO) /C-M(X) /Na(PO) /PK
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  242485. 2/28/96VtTransformations via Phosphorus-Stabilised Anions. 3. Reactions with Electrophiles other than  Aldehydes and Ketones.W
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  242487. GABRIEL WEATHERHEADy
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  242489. 19550
  242490. Schaumann, E.B
  242491. Heteroarenes III, Part 1K
  242492. Georg Thieme VerlagM
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  242498. GABRIEL WEATHERHEADy    Stuttgart
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  242500. Schaumann, E.B
  242501. Heteroarenes III, Part 1K
  242502. Georg Thieme VerlagM
  242503. 20560N
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  242505. 1,2-BenzoxazolesW
  242506. 1993X
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  242508. GABRIEL WEATHERHEADy    Stuttgart
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  242511. Pergamon PressM
  242512. 20561N
  242513. 2/28/96V    Azepines.W
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  242515. GABRIEL WEATHERHEADy
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  242517. 19553
  242518. Halton, B.B.Advances in Strain in Organic Chemistry, Vol 2K
  242519. Jai Pres  IncM
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  242522. 1992X
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  242524. GABRIEL WEATHERHEADy
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  242529. 2/28/96V>Cycloadditions of Ketenes and Keteniminium Salts with Alkenes.W
  242530. 1992Z
  242531. GABRIEL WEATHERHEADy
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  242534. Trost, B. M.//Fleming, I.B
  242535. Comprehensive Organic SynthesisC/C-C BOND FORMATION /ANNULATIONS /5-RING /6-RINGK
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  242538. 2/28/96V%The Prins and Carbonyl Ene Reactions.W
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  242540. GABRIEL WEATHERHEADy
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  242542. 19556
  242543. Trost, B. M.//Fleming, I.B
  242544. Comprehensive Organic SynthesisC7C-C BOND FORMATION /PERICYCLIC REACTIONS /ENE REACTIONSK
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  242547. 2/28/96V(Ene Reactions with Alkenes as Enophiles.W
  242548. 1991X
  242549. GABRIEL WEATHERHEADy
  242550. Oxford
  242551. 19557
  242552. Lindberg, T.B,Strategies and Tactics in Organic Synthesis.K
  242553. Academic PressM
  242554. 20566N
  242555. 2/28/96V`Evolution of a Synthetic Strategy, Part II: Total Synthesis of (-)-Casbene and (-)-Bertyadionol.W
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  242557. GABRIEL WEATHERHEAD
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  242560. Academic PressM
  242561. 20567N
  242562. 2/28/96VAEvolution of A Synthetic Strategy: Total Synthesis of Jatrophone.W
  242563. 1984Z
  242564. GABRIEL WEATHERHEAD
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  242567. Comprehensive Organic SynthesisC(C-C BOND FORMATION /APPENDAGES /COUPLINGK
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  242570. 2/28/96V-Coupling Reactions Between sp Carbon Centers.W
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  242572. GABRIEL WEATHERHEADy
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  242574. 19560
  242575. Trost, B. M.//Fleming, I.B
  242576. Comprehensive Organic SynthesisC(C-C BOND FORMATION /APPENDAGES /COUPLINGK
  242577. Pergamon PressM
  242578. 20569N
  242579. 2/28/96V5Coupling Reactions Between sp2 a d sp Carbon Centers.W
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  242581. GABRIEL WEATHERHEADy
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  242583. 19561
  242584. Liebeskind, L. S.B
  242585. Adv. Metal-Organic Chem.CUORGANOMETALLICS /CHROMIUM /C-C BOND FORMATION /AROMATICS /RING FUNCTIONALISATION  /CrK
  242586. Jai Press, Inc.M
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  242588. 2/28/96VAChiral Arene Chromium Carbonyl Complexes in Asymmetric Synthesis.W
  242589. 1989Z
  242590. GABRIEL WEATHERHEADy
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  242593. Trost, B. M.//Fleming, I.B
  242594. Comprehensive Organic SynthesisC;FUNCTIONAL GROUPS /P EPARATIONS /ORGANOSULPHUR COMPOUNDS /SK
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  242600. GABRIEL WEATHERHEADy
  242601. Oxford
  242602. 19563
  242603. Morrison, J. D.B
  242604. Asymmetric SynthesisC
  242605. C-C BOND FORMATION /APPENDAGES /1,2-ADDITION /ENANTIOGENIC REACTIONS /SULFOXIDES /C-X /SO /ENANTIOSELECTIVE /HETRING /3(O) /O=C(R)-C-C-X /OR(OH) /LACTONES  /5 /LACTONES /6 /SK
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  242607. 2/28/96V9Addition of Chiral Nucleophiles to Aldehydes and Ketones.W
  242608. 1983X
  242609. GABRIEL WEATHERHEADy
  242610. New York
  242611. 19564
  242612. Kreher, R. P.B
  242613. Heteroarenes II, Part 1K
  242614. Georg Thieme VerlagM
  242615. 20573N
  242616. 2/28/96V
  242617. 1-Benzothiopyrylium SaltsW
  242618. 1991X
  242619. 205-265Y
  242620. GABRIEL WEATHERHEADy    Stuttgart
  242621. 19565
  242622. Schaumann, E.B
  242623. Heteroarenes III, Part 2K
  242624. Georg Thieme VerlagM
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  242627. Indazoles (Benzopyrazoles)W
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  242630. GABRIEL WEATHERHEADy    Stuttgart
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  242632. Kreher, R. P.B
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  242634. Georg Thieme VerlagM
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  242651. Georg Thieme VerlagM
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  242679. Scheffold, R.B
  242680. Modern Synthetic Methods.C#ORGANOMETALLICS /SYNTHESIS /C-M /TMK
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  243568. GABRIEL WEATHERHEADy
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  243578. GABRIEL WEATHERHEADy
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  243585. GABRIEL WEATHERHEAD
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  243596. GABRIEL WEATHERHEADy    Stuttgart
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  243602. GABRIEL WEATHERHEAD
  243603. 19673
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  243605. Synthesis of Peptides Part IK
  243606. Georg Thieme VerlagM
  243607. 20682N
  243608. 2/28/96V?Blocking and Protection of the alpha-Amino Function in PeptidesW
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  243612. GABRIEL WEATHERHEADy    Stuttgart
  243613. 19674
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  243615. Synth sis of Peptides Part IK
  243616. Georg Thieme VerlagM
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  243619. Fundementals of Peptide Synthesis: Construction of Carboxamide Bond, Construction of Peptide  Bond and Preparation and Isolation of the "Free" PeptideW
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  243623. GABRIEL WEATHERHEADy    Stuttgart
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  243631. GABRIEL WEATHERHEADy
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  243636. Georg Thieme VerlagM
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  243639. Thioaldehydes and ThioketonesW
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  243682. Georg Thieme VerlagM
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  243755. 2/28/96V6Catalytic Reactions: Isomerizations and RearrangementsW
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  243757. GABRIEL WEATHERHEADy    Stuttgart
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  243790. Georg Thieme VerlagM
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  243792. 2/28/96V0Inorganic Sulfur Compounds as Oxidation ReagentsW
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  243796. GABRIEL WEATHERHEADy    Stuttgart
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  243800. Georg Thieme VerlagM
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  243803. 1988X
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  243805. GABRIEL WEATHERHEADy    Stuttgart
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  243818. Georg Thieme VerlagM
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  243820. 2/28/96VdGeneral Considerations, Nomenclature and Spectroscopic Identification of Organophosphorus  CompoundsW
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  243823. GABRIEL WEATHERHEADy    Stuttgart
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  243825. Regitz, M.
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  243827. Georg Thieme VerlagM
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  243832. GABRIEL WEATHERHEADy    Stuttgart
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  243836. Georg Thieme VerlagM
  243837. 20707N
  243838. 2/28/96VDPhosphorus(I) Compounds with Coordination / Number 1: PhosphinidenesW
  243839. 1982X
  243840. 15-19Y
  243841. GABRIEL WEATHERHEADy    Stuttgart
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  243845. Georg Thieme VerlagM
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  243850. GABRIEL WEATHERHEADy    Stuttgart
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  243854. Georg Thieme VerlagM
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  243859. GABRIEL WEATHERHEADy    Stuttgart
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  243869. GABRIEL WEATHERHEADy    Stuttgart
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  243874. 2/28/96V?The Effect of Fluorination of Enolates and Enolate Equivalents.W
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  243885. GABRIEL WEATHERHEADy
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  243888. Trost, B. M.//Fleming, I.B
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  243892. 2/28/96V%Heterodienophile Additions to Dienes.
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  243894. GABRIEL WEATHERHEADy
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  243902. GABRIEL WEATHERHEAD
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  243905. Carbenes (Carbenoids)K
  243906. Georg Thieme VerlagM
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  243912. GABRIEL WEATHERHEADy    Stuttgart
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  243914. Trost, B. M.//Fleming, I.B
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  243916. Pergamon PressM
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  243918. 2/28/96V1[3+2] and [5+2] Arene-Alkene Photocycloadditions.W
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  243920. GABRIEL WEATHERHEADy
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  243923. qA    Padwa, A.B
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  243927. 2/28/96V*Arene-alkene photocycloaddition reactions.W
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  243929. GABRIEL WEATHERHEADy
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  243936. 2/28/96V4Aromatic Compounds: Isomerisation and Cycloaddition.W
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  243945. Alkenes: Cycloaddition.W
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  243947. GABRIEL WEATHERHEAD
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  243951. Georg Thieme VerlagM
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  243957. GABRIEL WEATHERHEADy    Stuttgart
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  243961. Georg Thieme VerlagM
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  243969. Trost, B. M.//Fleming, I.B
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  243971. Pergamon PressM
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  243973. 2/28/96V0 xidative Coupling of Phenols and Phenol Ethers.W
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  243975. GABRIEL WEATHERHEADy
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  243977. 19714
  243978. Trost, B. M.//Fleming, I.B
  243979. Comprehensive Organic SynthesisC PHYSICAL ORGANIC /REARRANGEMENTSK
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  243984. GABRIEL WEATHERHEADy
  243985. Oxford
  243986. 19715
  243987. Trost, B. M.//Fleming, I.B
  243988. Comprehensive Organic SynthesisC"FUNCTIONAL GROUPS /TRANSFORMATIONSK
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  243994. GABRIEL WEATHERHEADy
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  244000. 2/28/96V[Methynolide and the Prelog-Djerasi Lactonic Acid: an Exercise in Stereocontroled Synthesis.W
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  244002. GABRIEL WEATHERHEAD
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  244009. Fragmentation Reactions.W
  244010.  991X
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  244012. GABRIEL WEATHERHEADy
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  244018. 2/28/96V'Exploration Towards Pseudomonic Acid C.W
  244019. 1988Z
  244020. GABRIEL WEATHERHEAD
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  244022. Werner, H.//Erker, G.B(Organometallics in Organic Synthesis. 2.C
  244023. ORGANOMETALLICS /NiK
  244024. SpringerM
  244025. 20728N
  244026. 2/28/96V&Organic Synthesis via Organometallics.W
  244027. 1989X
  244028. GABRIEL WEATHERHEADy
  244029. Berlin
  244030. 19720
  244031. ApSimon, J.B(The Total Synthesis of Natural Products.C(TARGET SYNTHESIS /MACROLIDES /IONOPHORESK
  244032. WileyM
  244033. 20729N
  244034. 2/28/96V"The Total Synthesis of Ionophores.W
  244035. 1981X
  244036. GABRIEL WEATHERHEAD
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  244038. Coxon, J. M.B!Adv. Detailed Reaction MechanismsK    Jai PressM
  244039. 20730N
  244040. 2/28/96
  244041. ~V3Mechanism of Cytochrome P-450 Catalyzed Oxid tions.W
  244042. 1992Z
  244043. GABRIEL WEATHERHEADy
  244044. Greenwich, CT
  244045. 19722
  244046. Suschitzky, H.//Scriven, E. F.B#Progress in Heterocyclic Chemistry,C
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  244048. 20731N
  244049. 2/28/96VHReactions of sulfinyl and sulfonyl carbanions with sulfenylating agents.W
  244050. 1993Z
  244051. GABRIEL WEATHERHEADy
  244052. Oxford, U.K.
  244053. 19723
  244054. Bartl, H.//Falbe, J.B
  244055. Macromolecular MaterialsM
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  244057. 2/28/96V-Polymers with C-Main Chains by PolymerizationW
  244058. 1987a
  244059. GABRIEL WEATHERHEAD
  244060. 19724
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  244063. Pergamon PressM
  244064. 20733N
  244065. 2/28/96V
  244066. Claisen Rearrangements.W
  244067. 1991X
  244068. GABRIEL WEATHERHEADy
  244069. Oxford
  244070. 19725
  244071. Scheffold, R.B
  244072. Modern Synthetic MethodsK
  244073. Verlag Helvetica Chimica ActaM
  244074. 20734N
  244075. 2/28/96V
  244076. Acetylenes in SynthesisW
  244077. 1992X
  244078. 103-226Z
  244079. GABRIEL WEATHERHEADy
  244080. Basel, Switzerland
  244081. 19726
  244082. Janoschek, R.
  244083. B1Chirality : from Weak Bosons to the Alpha - HelixK
  244084. SpringerM
  244085. 20735N
  244086. 2/28/96V+Preparation of Homochiral Organic CompoundsW
  244087. 1991X
  244088. 141-165a
  244089. GABRIEL WEATHERHEADy
  244090. Berlin
  244091. 19727
  244092. Trost, B. M.//Fleming, I.B
  244093. Comprehensive Organic SynthesisC)LITHIUM /Na /Mg /Ar-M /C=C-C-M /Li /C=C-MK
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  244095. 20736N
  244096. 2/28/96VTCarbanions of Alkali and Alkaline Earth Cations: (i) Synthesis and Characterisation.W
  244097. 1991X
  244098. GABRIEL WEATHERHEADy
  244099. Oxford
  244100. 19728
  244101. Trost, B. M.//Fleming, I.B
  244102. Comprehensive Organic SynthesisC3C-C BOND FORMATION /APPENDAGES /1,2-ADDIT ON /X-C-MK
  244103. Pergamon PressM
  244104. 20737N
  244105. 2/28/96V%Heteroatom-stabilized Allylic Anions.W
  244106. 1991X
  244107. GABRIEL WEATHERHEADy
  244108. Oxford
  244109. 19729
  244110. Trost, B. M.//Fleming, I.B
  244111. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APPENDAGES /1,2-ADDITIONK
  244112. Pergamon PressM
  244113. 20738N
  244114. 2/28/96V&Propargyl and Allenyl Organometallics.W
  244115. 1991X
  244116. GABRIEL WEATHERHEADy
  244117. Oxford
  244118. 19730
  244119. Trost, B. M.//Fleming, I.B
  244120. Comprehensive Organic SynthesisC,C-C BOND FORMATION /APPENDAGES /1,2-ADDITIONK
  244121. Pergamon PressM
  244122. 20739N
  244123. 2/28/96VCLewis Acid Promoted Addition Reactions of Organometallic Compounds.W
  244124. 1991X
  244125. GABRIEL WEATHERHEADy
  244126. Oxford
  244127. 19731
  244128. Oae, S.B
  244129. Rev. Heteroatom Chem.C
  244130. Ge /Sn /PbK
  244131. MYU K.K.M
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  244141. 20741N
  244142. 2/28/96V>Ylides stabilized by (fluoro, perfluoroalkyl) sulfonyl groups.W
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  244144. GABRIEL WEATHERHEAD
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  244147. Comprehensive Organic SynthesisC.C-C BOND FORMATION /AROMATICS /CHAIN EXTENSIONK
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  244149. 20742N
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  244151. The Reimer-Tiemann Reaction.W
  244152. 1991X
  244153. GABRIEL WEATHERHEADy
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  244155. 19734
  244156. Trost, B. M.//Fleming, I.
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  244158. ORGANOMETALLICS /Cr /QUINONESK
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  244162. Metal-Carbene Cycloadditions.W
  244163. 1991X
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  244165. GABRIEL WEATHERHEADy
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  244168. Liebeskind, L. S.B
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  244179. Georg Thieme VerlagM
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  244182. Organic HydroxylaminesW
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  244186. GABRIEL WEATHERHEADy    Stuttgart
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  244190. Georg Thieme VerlagM
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  244201. 20747N
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  244203. V=Skeletal Reorganizations: Chain Extension and Ring Expansion.W
  244204. 1991X
  244205. GABRIEL WEATHERHEADy
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  244209. Arenes and ArinesK
  244210. Georg Thieme VerlagM
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  244222. Hydroboration.W
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  244224. GABRIEL WEATHERHEADy
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  244233. GABRIEL WEATHERHEADy
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  244251. GABRIEL WEATHERHEADy
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  244260. GABRIEL WEATHERHEADy
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  244269. GABRIEL WEATHERHEADy
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  244275. 20755N
  244276. 2/28/96VAReduction o  C=X to CH2 by Dissolving Metals and Related Methods.W
  244277. 1991X
  244278. GABRIEL WEATHERHEADy
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  244282. Organometallics. A ManualC
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  244286. Organoaluminium CompoundsW
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  244297. GABRIEL WEATHERHEADy
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  244304. 2/28/96V,Compounds of Aluminium in Organic Synthesis.W
  244305. 1982X
  244306. GABRIEL WEATHERHEADy
  244307. Oxford
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  244310. CarbohydratesK
  244311. Kodansha LtdM
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  244321. Comprehensive Organic SynthesisM
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  244326. GABRIEL WEATHERHEAD
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  244333. 2/28/96VOPolyfluorinated 2,1,3-benzothia(selena)diazoles: heuristic and applied aspects.W
  244334. 1992Z
  244335. GABRIEL WEATHERHEADy
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  244340. Ge rg Thieme VerlagM
  244341. 20762N
  244342. 2/28/96VJCarbenes with Coordination Number 2: Methylene, Alkyl and Dialkyl CarbenesW
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  244346. GABRIEL WEATHERHEADy    Stuttgart
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  244349. Organic Peroxy CompoundsK
  244350. Georg Thieme VerlagM
  244351. 20763N
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  244353. 1988X    1123-1321Y
  244354. GABRIEL WEATHERHEADy    Stuttgart
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  244358. Georg Thieme VerlagM
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  244360. 2/28/96VMPeroxo Compounds as Reagents in Organic Chemistry: Reactions at a Hetero AtomW
  244361. 1988X    1321-1386Y
  244362.  4thZ
  244363. GABRIEL WEATHERHEADy    Stuttgart
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  244366. Carbocyclic pi-Electron SystemsK
  244367. Georg Thieme VerlagM
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  244370. AzulenesW
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  244374. GABRIEL WEATHERHEADy    Stuttgart
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  244377. CarbohydratesK
  244378. Kodansha LtdM
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  244380. 2/28/96V
  244381. Synthesis of Sialic Acid Analogs and Their Behavior Towards the Enzymes of Sialic Acid Metabolism and  Hemagglutinin X-31 of Influenza A-VirusW
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  244384. GABRIEL WEATHERHEADy
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  244387. Cadogan, J. I. G.B.Organophosphorus Reagents in Organic SynthesisCBC-C BOND FORMATION /HETEROANNULATIONS /P=N /C=C-X /P /HETEROCYCLESK
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  244389. 2/28/96V
  244390. Transformations via Phosphorus-Stabilised Anions.4.Heterocyclic Synthesis via  Alkylidenephosphoranes, Iminophosphoranes, and Vinylphosphonium Salts.W
  244391. 1979X
  244392. GABRIEL WEATHERHEADy
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  244413. GABRIEL WEATHERHEADy
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  244417. Organosulfur CompoundsK
  244418. Georg Thieme VerlagM
  244419. 20770N
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  244421. Sulfines and Their DerivativesW
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  244424. GABRIEL WEATHERHEADy    Stuttgart
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  244428. GABRIEL WEATHERHEAD
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  244435. The Di- -Methane Rearrangement.W
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  244437. GABRIEL WEATHERHEADy
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  244441. Bioorganic Chemistry FrontiersK
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  244443. 20773N
  244444. 2/28/96V[Mo ecular Tweezers: Synthetic Receptors for  -Sandwich Complexation of Aromatic Substrates.W
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  244446. GABRIEL WEATHERHEADy
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  244450. PergamonM
  244451. 20774N
  244452. 2/28/96V*Comprehensive Handbook of Hydrosilylation.W
  244453. GABRIEL WEATHERHEADy
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  244459. 2/28/96V6Chemistry of Organosulfur Compounds. General Problems.W
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  244468. 2/28/96V9Recent Advances in the Chemistry of 
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  244471. GABRIEL WEATHERHEADy
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  244484. 2/28/96V'Nucleic Acids in Chemistry and Biology.W
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  244486. GABRIEL WEATHERHEADy
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  244490. E sevierM
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  244492. 2/28/96V Preparative Acetylenic ChemistryW
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  244494. GABRIEL WEATHERHEADy
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  244500. 2/28/96V'Chirality in Drug Design and Synthesis.W
  244501. GABRIEL WEATHERHEADy
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  244506. 2/28/96V$Principles of Molecular Recognition.W
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  244512. Marcel DekkerM
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  244514. 2/28/96V
  244515. Phospholipids Handbook.W
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  244522. 2/28/96V.CRC Handbook of Chromatography: Carbohydrates.W
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  244524. GABRIEL WEATHERHEADy
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  244530. 2/28/96VaChirality in Industry: The Commercial Manufacture and Applications of Optically Active Compounds.W
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  244563. 2/28/96V*Small Ring Compounds in Organic Synthesis.W
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  244771. 2/28/96VJNaturally Occurring Benzodiazepines. Structure, Distribution and Function.W
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  245078. 2/28/96V$The Chemistry of the Carbonyl Group.W
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  245309. 2/28/96V:The Chemistry of Organic Selenium and Tellurium Compounds.W
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  245339. 2/28/96VcThe Conformational Analysis of Cyclohexenes, Cyclohexadienes, and Related Hydroaromatic  Compounds.W
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  245355. 2/28/96V!The Chemistry of the Cyano Group.W
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  245393. 2/28/96V'CRC Handbook of Organic Photochemistry.W
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  245400. 20892N
  245401. 2/28/96V
  245402. Organometallics in Synthesis.W
  245403. 1994a
  245404. GABRIEL WEATHERHEADy
  245405. Chichester, U.K.
  245406. 19884
  245407. Simonyi, M.K
  245408. Akademiai KiadoM
  245409. 20893N
  245410. 2/28/96V
  245411. Chiral Molecules.W
  245412. 1990a
  245413. GABRIEL WEATHERHEADy
  245414. Budapest, Hungary
  245415. 19885
  245416. "A    Smith, K.K
  245417. Ellis HorwoodM
  245418. 20894N
  245419. 2/28/96V2Solid Supports and Catalysts in Organic Synthesis.W
  245420. 1992a
  245421. GABRIEL WEATHERHEADy
  245422. Chichester, U.K.
  245423. 19886
  245424. Starks, C. M.C%ODDS AND ENDS /TECHNIQUES AND METHODSK
  245425. 20895N
  245426. 2/28/96V`Phase Transfer Catalysis: New Chemistry, Catalysts, and Applications., ACS Symposium Series 326.W
  245427. 1987a
  245428. GABRIEL WEATHERHEAD
  245429. 19887
  245430. Stirling, C. J. M.B&The Chemistry of the Functional GroupsK
  245431. WileyM
  245432. 20896N
  245433. 2/28/96V%The Chemistry of the Sulfonium Group.W
  245434. 1981a
  245435. GABRIEL WEATHERHEADy
  245436. New Yor
  245437. 19888
  245438. Stevenson, D.//Wilson, I. D.K
  245439. PlenumM
  245440. 20897N
  245441. 2/28/96V
  245442. Chiral Separations.W
  245443. 1988a
  245444. GABRIEL WEATHERHEADy
  245445. New York
  245446. 19889
  245447. Strukul, G.K
  245448. Kluwer Academic Publ.M
  245449. 20898N
  245450. 2/28/96V6Catalytic Oxidations with Hydrogen Peroxide as OxidantW
  245451. 1992a
  245452. GABRIEL WEATHERHEADy
  245453. Dordrecht, The Netherlands
  245454. 19890
  245455. Thomas, S. E.C
  245456. B /SiK
  245457. Oxford University PressM
  245458. 20899N
  245459. 2/28/96
  245460. 'V2Organic Synthesis: The Roles of Boron and Silicon.W
  245461. 1991a
  245462. GABRIEL WEATHERHEADy
  245463. New York
  245464. 19891
  245465. Townsend, L. B.//Tipson, R. S.K
  245466. WileyM
  245467. 20900N
  245468. 2/28/96V^Nucleic Acid Chemistry, Pt. 4. Improved and New Synthetic Procedures, Methods, and Techniques.W
  245469. 1991a
  245470. GABRIEL WEATHERHEADy
  245471. New York
  245472. 19892
  245473. Townsend, L. B.K
  245474. PlenumM
  245475. 20901N
  245476. 2/28/96V)Chemistry of Nucleosides and Nucleotides.W
  245477. 1991Z
  245478. GABRIEL WEATHERHEADy
  245479. New York
  245480. 19893
  245481. Townsend, L. B.K
  245482. Plenum PressM
  245483. 20902N
  245484. 2/28/96V)Chemistry of Nucleosides and Nucleotides.W
  245485. 1988Z
  245486. GABRIEL WEATHERHEADy
  245487. New York
  245488. 19894
  245489. Trogler, W. C.K
  245490. ElsevierM
  245491. 20903N
  245492. 2/28/96V!Organometallic Radical Processes.W
  245493. 1990a
  245494. GABRIEL WEATHERHEAD
  245495. 19895
  245496. ,A    Vo, D. T.K
  245497. WileyM
  245498. 20904N
  245499. 2/28/96VQChemical Analysis of Polycyclic Aromatic Compounds (Chemical Analysis, Vol. 101).W
  245500. 1989a
  245501. GABRIEL WEATHERHEADy
  245502. New York
  245503. 19896
  245504. Vicens, J.//Bohmer, V.K
  245505. KluweM
  245506. 20905N
  245507. 2/28/96
  245508. -V8Calixarenes. A Versatile Class of Macrocyclic Compounds.W
  245509. 1990a
  245510. GABRIEL WEATHERHEAD
  245511. 19897
  245512. Ward, D. J.K
  245513. ElsevierM
  245514. 20906N
  245515. 2/28/96VAPeptide Pharmaceuticals. Approaches to the Design of Novel Drugs.W
  245516. 1991a
  245517. GABRIEL WEATHERHEADy
  245518. New York
  245519. 19898
  245520. Wilman, D. E. V.C
  245521. TARGET SYNTHESISK
  245522. Blackie & Son Ltd.M
  245523. 20907N
  245524. 2/28/96V
  245525. Chemistry of Antitumour Agents.W
  245526. 1990a
  245527. GABRIEL WEATHERHEAD
  245528. 19899
  245529. Zabicky, J.B&The Chemistry of the Functional GroupsC]FUNCTIONAL GROUPS /TRANSFORMATIONS /OXIDATION /CHO TO COOR /O=C-R /O=C-H  /ALDEHYDES /KETONESK
  245530. WileyM
  245531. 20908N
  245532. 2/28/96V#The Chemistry of the Carbonyl GroupW
  245533. 1970Z
  245534. GABRIEL WEATHERHEADy
  245535. New York
  245536. 19900
  245537. Zabicky, J.B&The Chemistry of the Functional GroupsC(FUNCTIONAL GROUPS /PREPARATIONS /ALKENESK
  245538. WileyM
  245539. 20909N
  245540. 2/28/96V
  245541. The Chemistry of AlkenesW
  245542. 1970Z
  245543. GABRIEL WEATHERHEADy
  245544. New York
  245545. 19901
  245546. Zabicky, J.B&The Chemistry of the Functional Groups
  245547. 2CKFUNCTIONAL GROUPS /TRANSFORMATIONS /O=C-X TO O=C-Y /AMIDES /METALLATI N /LiK
  245548. WileyM
  245549. 20910N
  245550. 2/28/96V
  245551. The Chemistry of Amides.W
  245552. 1970a
  245553. GABRIEL WEATHERHEADy
  245554. New York
  245555. 19902
  245556. 3A2Yoshioka, M.//Parvez, S.//Miyazaki, T.//Parvez, H.K
  245557. 20911N
  245558. 2/28/96VMSupercritical Fluid Chromatography and Micro-HPLC (Progress in HPLC. Vol. 4).W
  245559. 1989a
  245560. GABRIEL WEATHERHEADy
  245561. Utrecht, The Netherlands
  245562. 19903
  245563. Y. Ito
  245564. AHTriol Synthesis
  245565. Silyl Baeyer-Villiger Oxidation
  245566. Amino-alcohol Synthesis
  245567. 20912N
  245568. 2/28/96V
  245569. Stereoselective Intramolecular Bis-Silyation of Alkenes Promoted by a Palladium -Isocyanide Catalyst Leading to Polyol SynthesisW
  245570. 1993X
  245571. 6487Y
  245572. Gabriel S weatherhead
  245573. JACSC0Cationic Cyclization
  245574. Stannic Chloride
  245575. AnnulationI
  245576. 20913N
  245577. 2/28/96VQSynthesis of rac-7,8-Epoxy-4-basmen-6-one by a Transannular Cyclization Strategy W
  245578. 1993X
  245579. 7926Y
  245580. A.G. MeyersB
  245581. JACSC-Radical Cyclization
  245582. Photochemical Annulation
  245583. 20914N
  245584. 2/28/96VDSynthesis of rac-7,8-Epoxy-4-basmen-6-one by a Transannular StrategyW
  245585. 1993X
  245586. 7926Y
  245587. K. C. Nicolaou et al.
  245588. JACSC3[3,3]-sigmatropic rearrangement
  245589. Glycoside coupling
  245590. 20915N
  245591. 2/28/96VVTotal Synthesis of Calicheamicin g1I .  1.  Synthesis of the Oligosaccharide Fragment.W
  245592. 1993X    7593-7611Y
  245593. K.C. NicolaouB
  245594. JACSC11,3-Dipolar Cycloaddition 
  245595. Nitrile Oxide
  245596. AldoximeI
  245597. 20916N
  245598. 2/28/96VkTotal Syntheis of Calicheamicin g1I.  2.  Development of an Enantioselective Route to (-)-Calicheamicinone.W
  245599. 1993X    7612-7624Y
  245600. K.B. SharplessB
  245601. JACSC?Osmium Tetroxide
  245602. Oxidation
  245603. OsO4-cinchona alkaliod catalystI
  245604. 20917N
  245605. 2/28/96VFKinetic Resolution of Racemic Olefins via Asymmetric Dihydroxylation. W
  245606. 1993X
  245607. 7864Y
  245608. J.S. PanekB
  245609. JACSC<b-hydroxyketone
  245610. 1,3-aminoalcohol
  245611. [3+2]-Dipolar Cycloaddition
  245612. 20918N
  245613. 2/28/96V
  245614. Asymmetric [3+2] D2-Isoxazoline Annulation by Electroplilic Substitution Of (E)-Crotylsilanes with Nitrosium Tetrafluoroborate.W
  245615. 1993X
  245616. 7898Y
  245617. A.G. SchultzB
  245618. JACSC
  245619. Alkylation
  245620. Birch ReductionI
  245621. 20919N
  245622. 2/28/96V`The First Asymmetric Synthesis of a Lycorine Alkaloid.  Total Synthesis of (+)-1-Deoxylycorine. W
  245623. 1993X
  245624. 7904Y
  245625. A.G. ShultzB
  245626. JACSC4Radical cyclization
  245627. Tributyltin hydride
  245628. Ring closureI
  245629. 20920N
  245630. 2/28/96V_The First Asymmetric Synthesis of a Lycorine Alkaloid.  Total Synthesis of (+)-1-Deoxylycorine.W
  245631. 1993X
  245632. 7904Y
  245633. K.C. NicolaouB
  245634. JACSC
  245635. Oligosaccaride
  245636. Glyoside
  245637. 20921N
  245638. 2/28/96V=Total Synthesis of Calicheamicin g 1I.  3.  The Final Stages.W
  245639. 1993X
  245640. 7625Y
  245641. H. YamamotoB
  245642. JACSCAtrioxane
  245643. ene reaction
  245644. olefins
  245645. enolates
  245646. Grignard reagentsI
  245647. 20922N
  245648. 2/28/96
  245649. Stabilization of Reactive Aldehydes by Complexation with Methylaluminum Bis(2,6-diphenylphenoxide) and their Synthetic Application W
  245650. 1993X
  245651. 3943Y
  245652. 115 #10
  245653. T. CohenB
  245654. JACSC4homoallylic sulfides
  245655. cyclopropylcarbinyllithiumI
  245656. 20923N
  245657. 2/28/96V
  245658. Generation, Some Synthetic Uses, and 1,2-Vinyl Rearrangements of Secondary and Tertiary Homoallyllithiums, Including Ring Contractions and A Ring Expansion.  Remarkable Acceleration of the Rearrangement by an Oxyanionic Group.W
  245659. 1993X
  245660. 3855Y
  245661. 115 #10
  245662. M.P. DoyleB
  245663. JACSC6Rhodium Carbene Complex
  245664. g-Lactone Synthesis
  245665. diazoesterI
  245666. sKgStudy of the preference of C-H insertion of tertiary vs. secondary vs. primary and benzylic C-H bonds  M
  245667. 20924N
  245668. 2/28/96V
  245669. Electronic and Steric Control In C-H Insertion Reactions of Diazoacetoacetates Catalyzed by Dirhodium (II) Carboxylates and Carboxamides W
  245670. 1993X
  245671. H.YamamotoB
  245672. JACSCIChiral Imine
  245673. Binaphthol-Triphenylborate
  245674. b-Lactam Synthesis
  245675. Ketene Acetal
  245676. 20925N
  245677. 2/28/96V|Highly Selective and Operationally Simple Synthesis of Enantiomerically Pure b-Amino Esters via Double StereodifferentiationW
  245678. 1993X
  245679. 1151Y
  245680. G. MolanderB
  245681. JACS C;Ketene Acetal 
  245682. Diketone
  245683. Ketoaldehyde
  245684. TrimethylsilyltriflateI
  245685. 20926N
  245686. 2/28/96V
  245687. Neighbouring Group Participation in Lewis Acid-Promoted [3+4] and [3+5] Annulations.  The Synthesis of Oxabicyclo[3.n.1]alkan-3-onesW
  245688. 1993X
  245689. S. KimB
  245690. Tet. LettersC&Tributyltin Hydride
  245691. Epoxide
  245692. AnnulationI
  245693. 20927N
  245694. 2/28/96V>Stereoselective Radical Cyclization of Epoxy Silyl Enol EthersW
  245695. 1992X
  245696. 7391Y
  245697. J.C. CarreteroB
  245698. Tet. LettersC7Trimethyl Aluminum
  245699. Chelation Control
  245700. Conjugate AdditionI
  245701. 20928N
  245702. 2/28/96VBA Novel Stereoselective Synthesis of Substituted g-Butyrolactones W
  245703. 1992X
  245704. 7407Y
  245705. W.D. WulffB
  245706. JACSC;Chromium Carbene Complex
  245707. Butenolide Synthesis
  245708. Ketene AcetalI
  245709. xK<order of insertion :  allyl/benzyl>methylene>methine>methyl M
  245710. 20929N
  245711. 2/28/96
  245712. EVPC-H Insertions in the reactions of Fischer Carbene Complexes with Ketene AcetalsW
  245713. 1992X
  245714. 10665Y
  245715. FA    W.D.WulffB
  245716. JACSCBChromium Carbene Complexes
  245717. Acetylene
  245718. TBSOTf
  245719. Iodine
  245720. annulation
  245721. 20930N
  245722. 2/28/96V]Sequential Benzannulation / Nucleophilic Aromatic Addition Reactions Mediated by Chromium (0)W
  245723. 1992X
  245724. 10667Y
  245725. P. KnochelB
  245726. JOCCXChromium Chloride
  245727. Lithium Chloride
  245728. Allylic Phosphates
  245729. Homoallylic Alcohol SynthesisI
  245730. zKtReview: N. A. Saccomano In Comprehensive Organic Synthesis; B. M. Trost ; Ed.; Pergamon Press: Oxford,1991, p 173.
  245731. 20931N
  245732. 2/28/96VIStereodivergent Additions of Allylic Chromium (III) Reagents to AldehydesW
  245733. 1992X
  245734. 6384Y
  245735. H. YamamotoB
  245736. JOCC!Barium Iodide
  245737. Lithium BiphenylideI
  245738. {KyREVIEW: D. C. Billington, In Comprehensive Organic Synthesis; B. M. Trost;Ed.; Pergamon Press: Oxford, 1991,vol.3, p 413.M
  245739. 20932N
  245740. 2/28/96VMHighly Selective Homocoupling Reaction of Allylic Halides Using Barium Metal W
  245741. 1992X
  245742. C. KibayashiB
  245743. JACSCKChromium Chloride
  245744. Nickel Chloride
  245745. Allylic Alcohol Synthesis
  245746. Nozaki ReactionI
  245747. JACS 1986,108, 6048
  245748. 20933N
  245749. 2/28/96VD
  245750. Higly Stereocontrolled Total Synthesis of (+)-Allopumiliotoxin 339AW
  245751. 1992X
  245752. 10653Y
  245753. L.A. PaquetteB
  245754. JACSC
  245755. Cuprate
  245756. Me2CuLi
  245757. 20934N
  245758. 2/28/96V'Total Synthesis of (-)-Subergorgic AcidW
  245759. 1993X
  245760. L.S. HegedusB
  245761. JACSC
  245762. Photochemistry
  245763. 20935N
  245764. 2/28/96VqSynthesis of Compounds Containing Two Adjacent 13C Labels by Photolytic Reactions of Chromium Carbene Complexes  W
  245765. 1993X
  245766. E. NakamuraB
  245767. JACSI
  245768. 20936N
  245769. 2/28/96V
  245770. Theoretical Studies on Carbometalation of Cyclopropene.  Transistion Structures of Me-, MeLi, MeCu, and Me2Cu- and the Orgin of the High Reactivity of the Strained Double Bond  W
  245771. 1993X
  245772. S. DanishefskyB
  245773. JACS C=Aza-Robinson Annulation
  245774. Rhodium Acetate
  245775. Diazoketone
  245776. TholactamI
  245777. 20937N
  245778. 2/28/96
  245779. MV Total Synthesis of IndolizomycinW
  245780. 1993X
  245781. G.A. MolanderB
  245782. JACSCPChiral Acetoxy Acetals
  245783. Cyclic Oxonium Ion
  245784. Lewis Acid
  245785. TMSCN
  245786. AllyltributylstannaneI
  245787. JACS 1991, 113, 3608M
  245788. 20938N
  245789. 2/28/96VYNovel Approach to Remote Asymmetric Induction in Carbonyl Addition and Related Reactions W
  245790. 1993X
  245791. L.A. PaquetteB
  245792. JACSCYLewis Acid Mediated Aldol
  245793. Mukaiyama Aldol
  245794. Silyl Enol Ether
  245795. Titanium Tetrachloride
  245796. Acetal I
  245797. 20939N
  245798. 2/28/96V8Enantioselective Total Synthesis of (-)-Subergorgic AcidW
  245799. 1993X
  245800. S. MuraiB
  245801. JACS C,Hydrosilation
  245802. Silyl Enol Ether
  245803. CarbonylationI
  245804. 20940N
  245805. 2/28/96V
  245806. Conversion of Alkanes to Enol Silyl Ethers of Acyl Silanes by Iridium-Catalyzed Reaction with a Hydrosilane and Carbon Monoxide.  W
  245807. 1992X
  245808. 9710Y
  245809. E. NakamuraB
  245810. JACSCLTributyltin Hydride
  245811. Chromium Carbene Complex
  245812. Michael Addition
  245813. Tin Chemistry I
  245814. 20941N
  245815. 2/28/96
  245816. QVa1,2-Asymmetric Induction in the Sn-H Bond Insertion Reaction of Aliphatic Fischer Carbene ComplexW
  245817. 1992X
  245818. 9715Y
  245819. K.A. ParkerB
  245820. JACSC(Radical Cyclization 
  245821. Tributyltin HydrideI
  245822. 20942N
  245823. 2/28/96V
  245824. Formal Synthesis rac-MorphineW
  245825. 1992X
  245826. 9688Y
  245827. T. HudlickyB
  245828. JACSC-Heck Coupling
  245829. Palladium Mediated Cyclization
  245830. 20943N
  245831. 2/28/96V%A Short Synthesis of (+)-LycoricidineW
  245832. 1992X
  245833. 9694Y
  245834. D.A. EvansB
  245835. JACSC9Titanium Oxazolidinone Enolate
  245836. Asymmetric Aldol Reaction
  245837. K=D. A. Evans JACS 1990,112, 866 and Tetrahedron 1992,48, 2127.M
  245838. 20944N
  245839. 2/28/96V#Total Synthesis of (+)-Calyculin A.W
  245840. 1992X
  245841. 9434Y
  245842. D.A. EvansB
  245843. JACSC;Lithium Phosphonate
  245844. Olefin Synthesis
  245845. Horner Emmons ReactionI
  245846. 20945N
  245847. 2/28/96V"Total Synthesis of (+)-Calyculin AW
  245848. 1992X
  245849. 9434Y
  245850. D.A. EvansB
  245851. JACSC2Aldol Reaction
  245852. Silyl Enol Ether
  245853. Felkin SelectivityI
  245854. K%C. H. Heathcock JACS 1983, 105, 1667.M
  245855. 20946N
  245856. 2/28/96
  245857. VV"Total Synthesis of (+)-Calyculin AW
  245858. 1992X
  245859. 9434Y
  245860. B.M. TrostB
  245861. JACSI
  245862. 20947N
  245863. 2/28/96V}A Modular Approach for Ligand Design for Asymmetric Allylic Alkylations via Enantioselective Palladium-Catalyzed Ionizations.W
  245864. 1992X
  245865. 9327Y
  245866. A.G. MeyersB
  245867. JACSC
  245868. Bergman CyclizationI
  245869. 20948N
  245870. 2/28/96VUStudies on the Thermal Generation and Reactivity of a Class of (s,p)-1,4-Biradicals. W
  245871. 1992X
  245872. 9369Y
  245873. A.G. MeyersB
  245874. JACSC
  245875. Bergman CyclizationI
  245876. 20949N
  245877. 2/28/96V
  245878. Synthesis of 1,6-Didehydro[10]annulene.  Observation of its Exceptionally Facile Rearrangement to the Biradical 1,5-Dehydronaphthalene.W
  245879. 1992X
  245880. 10986Y
  245881. T. SammmakiaB
  245882. JACSC2Allyltributylstannane
  245883. Lewis acid
  245884. Titanium CatalystI
  245885. 20950N
  245886. 2/28/96VcDirect Evidence for an Oxocarbenium Ion Intermediate in the Asymmetric Cleavage of Chiral Acetals. W
  245887. 1992X
  245888. 10998Y
  245889. E. LeeB
  245890. JACSC88 Membered Cyclic Lactone Synthesis
  245891. Tributyltin hydride
  245892. 20951N
  245893. 2/28/96VS8-Endo Cyclization of (Alkoxycarbonyl)methyl Radicals Generated from Bromoacetates.W
  245894. 1992X
  245895. 10981Y
  245896. D.L. CominsB
  245897. JACSCPPyridine Chemistry
  245898. Grignard Reagent
  245899. Allylsilane
  245900. Cuprate
  245901. Silicon Protecting GroupI
  245902. 20952N
  245903. 2/28/96V
  245904. Stereoselective Addition of (Triphenylsilyl)magnesium Bromide to Chiral 1-Acyl-4-methoxypyridinium Salts.  Synthesis and Reactions of Enantiopure 1-Acyl-2-(triphenylsilyl)-2,3-dihydro-4-pyridones. W
  245905. 1992X
  245906. 10972Y
  245907. D.L. CominsB
  245908. JACSCSLithium Halogen Exchange
  245909. Diastereoselective Nucleophilic Addition to Chiral KetonesI
  245910. 20953N
  245911. 2/28/96V5A 10 Step, Asymmetric  Synthesis of (S)-Camptothecin W
  245912. 1992X
  245913. 10971Y
  245914. P. WipfB
  245915. JACSC!Oxazoline
  245916. Peptide
  245917. Burgess ReagentI
  245918. K"P. Wipf TL 1992, 33, 907 and 6267.M
  245919. 20954N
  245920. 2/28/96V!Total Synthesis of Westiellamide.W
  245921. 1992X
  245922. 10975Y
  245923. D.L. CominsB
  245924. JACSC@Heck reaction
  245925. Palladium Catalyzed Cyclization
  245926. Palladium Acetate
  245927. _K#R. Grigg Tetrahedron 1990, 46,4003.M
  245928. 20955N
  245929. 2/28/96V3A 10 Step, Asymmetric Synthesis of (S)-CamptothecinX
  245930. 10971Y
  245931. W.D. WulffB
  245932. JACS CFChromium Carbene Complex
  245933. Tungsten Carbene Complex
  245934. Danishefsky's Diene
  245935. KpW. D. Wulff  In Comprehensive Organic Synthesis; Trost, Fleming,Eds.;Pergamon Press: N.Y.,1991;Vol. 5, pp1065. 
  245936. 20956N
  245937. 2/28/96V>Exo-Selective Diels-Alder Reactions of Aminocarbene Complexes.W
  245938. 1992X
  245939. 10784Y
  245940. B.M. TrostB
  245941. JACSC
  245942. Isocyanate
  245943. Carbonate
  245944. CarbamateI
  245945. K6Trost B. M.  Angew. Chem. Int. Ed. Engl. 1992,31, 228.M
  245946. 20957N
  245947. 2/28/96V
  245948. A general Synthetic Strategy toward Amimocyclopentitiol Gylcosidase Inhibitors.  Application of Palladium Catalysis to the Synthesis of Allosamizoline and Mannostatin A.W
  245949. 1993X
  245950. 115 (2)
  245951. W.S. JohnsonB
  245952. JACSI
  245953. see previous 3 papersM
  245954. 20958N
  245955. 2/28/96VwThe Fluorine Atom as a Cation-Stabilizing Auxiliary in Biomimetic Polyene Cyclizations.  Total Synthesis of dl-b-AmyrinW
  245956. 1993X
  245957. 115(2)
  245958. W.S. JohnsonB
  245959. JACSC?Palladium Catalyzed Alkylation 
  245960. Allylic Acetate
  245961. Beta-Keto EsterI
  245962. K7see previous 3 papers
  245963. Trost B. M. JACS 1980, 102, 4730
  245964. 20959N
  245965. 2/28/96V*Fluorine in Total Synthesis of dl-b-AmyrinW
  245966. 1993X
  245967. 115(2)
  245968. N.L. BauldB
  245969. JACSC"Diels-Alder
  245970. Cyclobutane Synthesis
  245971. Tetrahedron 1989, 45, 5307.M
  245972. 20960N
  245973. 2/28/96V^Cation Radical Probes. Development and Application to Matalloporphyrin-Catalyzed Epoxidation. W
  245974. 1992X
  245975. 10968Y
  245976. S.J. DanishefskyB
  245977. JACSC@cyclopropane synthesis
  245978. Allyl Stannane
  245979. Trimethyl Stannyl Lithium I
  245980. K5Still JACS 1977,99,4836.
  245981. T. Ishii JOC 1987, 52, 4416.M
  245982. 20961N
  245983. 2/28/96VAA Remarkable Cyclopropanation: The Total Synthesis of Myrocin C. W
  245984. 1992X
  245985. 8333Y
  245986. S.J. DanishefskyB
  245987. JACSC
  245988. Intramolecular Diels-Alder
  245989. 20962N
  245990. 2/28/96V
  245991. Total Synthesis of Myrocin C.W
  245992. 1992X
  245993. 8333Y
  245994. Y. ItoB
  245995. JACSI
  245996. K*Y. Ito Tetrahedron Asymmetry 1991, 2, 593.M
  245997. 20963N
  245998. 2/28/96
  245999. Catalytic Asymmetric Synthesis with Trans Chelating Chiral Diphosphine Ligand TRAP: Rhodium Catalyzed Asymmetric Michael Addition of a-Cyano Carboxylates.  W
  246000. 1992X
  246001. 8295Y
  246002. D. CrichB
  246003. JACS I
  246004. 20964N
  246005. 2/28/96VtThe Chemistry of Acyl Tellurides: Generation and Trapping of Acyl Radicals , Including Aryltellurium Group Transfer.W
  246006.  1992X
  246007. 8313Y
  246008. A.B. Smith (the unnovel one)B
  246009. JACSCIDialkyl zinc
  246010. Conjugate Addition
  246011. Aldol Condensation
  246012.  Zinc Enolate TrappingI
  246013. KMR. Noyori Angew. Chem. Int. Ed. Engl.1984,23,847.
  246014. Chem. Ber. 1986, 119, 1581.M
  246015. 20965N
  246016. 2/28/96V#Total Synthesis of (+)-HitachimycinW
  246017. 1992X
  246018. 8008Y
  246019. E.J. CoreyB
  246020. JACSCZAsymmetric Diels-Alder reaction
  246021. Chiral Dioxaborolidine Catalyst
  246022. Boron Lewis Acid Catalyst
  246023. K!E. J. Corey JACS 1991, 113, 8966.M
  246024. 20966N
  246025. 2/28/96V
  246026. The Orgin of  Greater Than 200:1 Enantioselectivity in a Catalytic Diels-Alder Reaction As Revealed by Physical And Chemical Studies.W
  246027. 1992X
  246028. 8290Y
  246029. A. Ogawa
  246030. N. SonodaB
  246031. JACSC<Samarium Iodide
  246032. Amide
  246033. Diaminoalkene Synthesis
  246034. radical anion
  246035. 20967N
  246036. 2/28/96V5Deoxygenative Coupling of Amides by a Sm/SmI2 System.W
  246037. 1992X
  246038. 8729Y
  246039. K. TomiokaB
  246040. JACSC.Organolithium Species
  246041. Organotellurium Species
  246042. 20968N
  246043. 2/28/96VZA Catalytic Method for Asymmetric Nucleophilic Aromatic Substitution Giving Binaphthyls.  W
  246044. 1992X
  246045. 8732Y
  246046. E. NakamuraB
  246047. JACSCwFive(5) membered Carbocycle Synthesis
  246048. Thermal  [3+2] Cycloaddition
  246049. (E)-Ethylidenecyclopropane
  246050. Electron-Deficient OlefinI
  246051. ref. (1) E. Nakamura JACS 1991, 113, 3183. (2) JACS 1989, 111, 7285. (3) JOC 1990,55,5553. (4) 'Organic Synthesis in Japan, Past, Present, and Future; R. Noyori, Ed. 1992 pp 273. M
  246052. 20969N
  246053. 2/28/96VwRegioselective and Endo-Stereoselective [3+2] Cycoaddition of Dipolar Trimethylenemethane to Electron-Deficient Olefin.W
  246054. 1992X
  246055. 8707Y
  246056. C. A. Merlic*B
  246057. JACSCAAromatic Ring Synthesis
  246058. Amide Synthesis
  246059. Napthalene ring synthesis
  246060. K*Ref.; (1) C.A. Merlic JACS 1991,113, 7418.M
  246061. 20970N
  246062. 2/28/96VSAminobenzannulation via Metathesis of Isonitriles Using Chromium Carbene Complexes.W
  246063. 1992X
  246064. 8723Y
  246065. A.I. MeyersB
  246066. JACSC1Metalation
  246067. Benzyne Cyclization
  246068. Alkaloid SynthesisI
  246069. 20971N
  246070. 2/28/96VpCryptaustoline: Synthesis, Revision of Absolute Stereochemistry, and Mechanism of Inversion of Stereochemistry. W
  246071. 1992X
  246072. 8483Y
  246073. A.I. MeyersB
  246074. JACSC]Asymmetric Alkylation
  246075. Metalation
  246076. Chiral Isoquinoline Formamidine
  246077. Carbanion
  246078. Alkaloid SynthesisI
  246079. KJ(1) Meyers Tetrahedron 1987, 43, 5095. (2) Meyers JOC 1991, 56, 2091,6873 M
  246080. 20972N
  246081. 2/28/96VoCryptaustoline: Synthesis, Revision of Absolute Stereochemistry, and Mechanism of Inversion of Stereochemistry.W
  246082. 1992X
  246083. 8483Y
  246084. S.P. TanisB
  246085. JACSCmFuran
  246086. Mercury mediated cyclization
  246087. mercuric trifluoroacetate
  246088. Intramolecular Friedel Crafts reaction
  246089. thioesterI
  246090. Other References: (1) S. Masamune JACS 1977, 99, 6756. (2) S. Masamune JACS 1975, 97, 3515.
  246091. (3) M. Nishizawa T.L. 1983, 24,2581. (4) M. Nishizawa JOC 1987, 52, 4878.   
  246092. 20973N
  246093. 2/28/96V5Furans In Synthesis: Total Synthesis of Fastigilin C W
  246094. 1992X
  246095. 8349Y
  246096. L.A. PaquetteB
  246097. JACS  CGAllyl stannane
  246098. Homoallylic alcohol synthesis
  246099. Aldehyde condensation
  246100. 20974N
  246101. 2/28/96W
  246102. 1992X
  246103. 3910Y
  246104. L. A. PaquetteB
  246105. JACSC>Palladium Coupling
  246106. Vinyl Stannane
  246107. Aryl halide
  246108. Olefin SynthesisI
  246109. 20975N
  246110. 2/28/96W
  246111. 1992X
  246112. 3910Y
  246113. D. SeebachB
  246114. Chem. Ber.CDMichael addition
  246115. conjugate addition
  246116. asymmetric 1,4- addition
  246117. enolateI
  246118. 20976N
  246119. 2/28/96W
  246120. 1991X
  246121. 1845Y
  246122. R. BrucknerB
  246123. Chem. Ber.C8organocopper
  246124. Wittig
  246125. Ylide
  246126. diene synthesis
  246127. copper
  246128. cuprateI
  246129. 20977N
  246130. 2/28/96W
  246131. 1991X
  246132. 1871Y
  246133. N. K. KocherkovetB
  246134. Carbohydrate ResearchCFGlycoside coupling
  246135. Sugar chemistry
  246136. Carbohydrate chemistry
  246137. Disaccaride
  246138. 20978N
  246139. 2/28/96
  246140. 1991X
  246141. D. SeebachB
  246142. Chem. Ber.C=Asymmetric alkylation
  246143. P4 base
  246144. hyroxy acid synthesis
  246145. enolate
  246146. 20979N
  246147. 2/28/96W
  246148. 1991X
  246149. 1837Y
  246150. K.P.C. VollhardtB
  246151. Angew.  Chem. Int. Ed. Engl. C(annulation
  246152. Cobalt cyclization
  246153. acetylene
  246154. 20980N
  246155. 2/28/96W
  246156. 1991X
  246157. yA    A. SuzukiB
  246158. Bull. Chem. Soc. Jpn.COpalladium coupling
  246159. vinyl iodide
  246160. carbon monoxide
  246161. unsaturated ketone
  246162. organoboraneI
  246163. 20981N
  246164. 2/28/96W
  246165. 1991X
  246166. 1999Y
  246167. vinyl iodide -> ketone
  246168. K. NarasakaB
  246169. Bull.Chem. Soc. Jpn.CEenamine
  246170. titanium complex
  246171. asymmetric Michael Addition
  246172. chiral auxillaryI
  246173. 20982N
  246174. 2/28/96W
  246175. 1991X
  246176. 2122Y
  246177. {A<Snider, Barry B.
  246178. Wan, B. Y-F.
  246179. Buckman, B. O.
  246180. Foxman, B. M.
  246181. JOCCJmanganese triacetate
  246182. oxidations
  246183. free radical cyclization
  246184. b-keto sulfoxidesI
  246185. 20983N
  246186. 2/28/96VeManganese(III)-Based Asymmetric Oxidative Free-Radical Cyclization of Unsaturated b-Keto Sulfoxides  W
  246187. 1991X
  246188. 328-338Y
  246189. |A!Snider, Barry B.
  246190. Allentoff, A. J.B
  246191. JOCC&Taxanes
  246192. oxy-Cope
  246193. Taxinine
  246194. vinyllithiumI
  246195. 20984N
  246196. 2/28/96VISynthesis of the Bicycl[5.3.1]undecane Moiety (AB Ring System) of TaxanesW
  246197. 1991X
  246198. 321-328Y
  246199. Inoue, S.
  246200. Sato, Y.
  246201. JOCC\Peterson olefination
  246202. germanium
  246203. silicon
  246204. ester enolates
  246205. aldol condensation
  246206. elimanation
  246207. olefinsI
  246208. The trimethylsilyl analogue gives mixtures of E/Z olefin geometries upon elimination due to migration of the silicon to the negatively charged oxygen of the aldolate resulting in an oxy anion due to the high affinity of silicon for oxygen, which is not shared with germanium.
  246209. 20985N
  246210. 2/28/96VvPeterson Olefination Reaction Using (Trimethylgermyl)acetate.  Stereoselective Synthesis of (E)-2-Alkenoic Acid EstersW
  246211. 1991X
  246212. 347-352Y
  246213. Wuts, Peter G. M.
  246214. Jung, Y-W.
  246215. JOCCHg-trimethylsilyl allyl boronates
  246216. silicon 
  246217. boron
  246218. imines
  246219. boron ate complexI
  246220. Reaction also works well for chiral a-alkoxyimines, where anti/syn stereochemistry predominates.  Anti between the alkoxy substituent and the nitrogen, and syn between the nitrogen and the siliyl substituent.M
  246221. 20986N
  246222. 2/28/96V:The Addition of g-(Trimethylsilyl)allylboronates to IminesW
  246223. 1991X
  246224. 365-372Y
  246225. A&Bell, S. I. 
  246226. Parvez, M.
  246227. Weinreb, S. M.B
  246228. JOCCxmetalation
  246229. alkylation
  246230. Diels-Alder
  246231. cycloaddition
  246232. pyrroles
  246233. sulfur stabilized carbanion
  246234. a-lithio sulfoxides
  246235. anomeric effectI
  246236.     The S-O bond sits axially disposed and a proposed sulfur stabilized carbanion, where the Li chelates to the oxygen of the sulfoxide, directs electrophilic attack to the face opposite the O of the sulfoxide.  BnBr is therefore more selctive due to a steric effect.  
  246237. 20987N
  246238. 2/28/96VzMetalation and Alkylation of 3,6-Dihydrothiazine-1-Oxides Prepared via Diels-Alder Cycloadditions of N-Sulinyl DienophilesW
  246239. 1991X
  246240. 373-377 Y
  246241. Racherla, U. S. 
  246242. Brown, H. C.
  246243. CNorganoborane
  246244. allylboration
  246245. Grignard reagent
  246246. salt free
  246247. condensation
  246248. ate complexI
  246249. Magnesium salts slow down the reaction to 5-7 hrs at -100
  246250. C due to the formation of a Mg ate complex with the B which is unreactive and more stable as the temperature is lowered.M
  246251. 20988N
  246252. 2/28/96V
  246253. Chiral Synthesis via Organoboranes. 27. Remarkably Rapid and Exceptionally Enantioselective ( Approaching 100% ee) Allylboration of Representative Aldehydes at -100
  246254. C under New Salt Free Conditions.W
  246255. 1991X
  246256. 401-404Y
  246257. A&Keck, G. E.
  246258. Andrus, M. B.
  246259. Romer, D. R.B
  246260. JOCCnmagnesium bromide etherate
  246261. benzyl ether
  246262. selective reduction
  246263. aldehyde
  246264. chelation control
  246265. vinyl metal
  246266. allyl metalI
  246267. 9A small amount of alcohol is also formed in the reduction, but only a to the OBn group.  The use of 2 equivalents of DIBAL will give selectively the alcohol a to the OBn at -40
  246268. C.  This a-benzyloxy aldehyde is also used in chelation controlled additions of allyl and vinyl metals to give selectively syn adducts. 
  246269. 20989N
  246270. 2/28/96V~A useful New Enantiomerically Pure Synthon from Malic Acid:  Chelation-Controlled Activation as a Route to Regioselectivity.  W
  246271. 1991  X
  246272. 417-420 Y
  246273. A&Potin, D.
  246274. Williams, K.
  246275. Rebek, J., Jr.
  246276. Angew. Chem. Int. Ed. Engl.C
  246277. enolate
  246278. asymmetric protonationI
  246279. 20990N
  246280. 2/28/96V#Asymmetric Protonation of Enolates
  246281. 1990X    1420-1421Y
  246282. Hoppe, D.
  246283. Hintze, F.
  246284. Tebben, P.B
  246285. Angew. Chem. Int. Ed. Engl.Cdasymmetric deprotonation
  246286. a-hydroxy acid
  246287. secondary alcohol
  246288. carbamate hydrolysis
  246289. cbx protecting group I
  246290. 20991N
  246291. 2/28/96V
  246292. Chiral Lithium-1-Oxyalkanides by Asymmetric Deprotonation; Enantioselective Synthesis of 2-Hydroxyalkanoic Acids and Secondary AlkanolsW
  246293. 1990X    1422-1424Y
  246294. A!Hoppe, D.
  246295. Carstens, A.
  246296. Kramer, T.I
  246297. 20992N
  246298. 2/28/96V
  246299. Generation of a Configurationally Stable Chiral Benzyllithium Derivative, and the Capricious Stereochemistry of its Electrophilic Substitution
  246300. Toshima, K.
  246301. Tatsuta, K.
  246302. Tet. Lett.C
  246303. diethylisopropylsilyl ether
  246304. protecting group
  246305. t-butyldimethylsilyl ether
  246306. t-butyldiphenylsilyl ether
  246307. silyl ether
  246308. hydrogenation
  246309. benzyl etherI
  246310. The diethylisopropylsilyl ether (DEIPS) is selectively cleaved in the presence of TBS and TBDPS groups in methanol; however in dioxane the DEIPS group remains intact whereas benzyl ethers are cleavedM
  246311. 20993N
  246312. 2/28/96W
  246313. 1990X    6697-6698Y
  246314. Tanaka, H.
  246315. Torii, S.B
  246316. Tet. Lett.C{protecting group
  246317. ester hydroylsis
  246318. p-methoxybenzyl ester
  246319. diphenylmethyl ester
  246320. t-butyl ester
  246321. benzyl ester
  246322. p-nitrobenzyl esterI
  246323. HCl, H2SO4, KHSO4 and TsOH were also effective in place of TFA.  Deprotection even occurs without the acid catalyst (60
  246324. C / 3 hr / 96%).  Cleaveage of diphenylmethyl and t-butyl esters was also successful, but benzyl and p-nitrobenzylesters remained intact
  246325. 20994N
  246326. 2/28/96W
  246327. 1990X    6661-6662Y
  246328. Nakamura, N.
  246329. Tet. Lett.
  246330. C]protecting group
  246331. 3-isoxazolyl ether
  246332. reduction
  246333. hydrogenolysis
  246334. trityl ether
  246335. Mitsunobu inversionI
  246336. KmPart of a two step epimerization of secondary hydroxyl groups via Mitsunobu inversion with 3-hydroxyisoxazoleM
  246337. 20995N
  246338. 2/28/96W
  246339. 1990X
  246340. 699-702Y
  246341. Bose, D. S.
  246342. Thurston. D. E.B
  246343. Tet. Lett.CWprotecting group
  246344. hydrolysis
  246345. boron trifluoride etherate
  246346. ethanethiol
  246347. CBZ group
  246348. carbamate
  246349. This method avoids the reduction of olefins, acetylenes, ketones, imines, halides or nitro groups and the hydrolysis of esters.  The use of neat reagents facilitated the removal of primary carbamates. M
  246350. 20996N
  246351. 2/28/96W
  246352. 1990X    6903-6906Y
  246353. A9van der Baan, J. L.
  246354. Barnick, J. W. F. K.
  246355. Bickelhaupt, F.
  246356. B)Synthesis  (Journal of Synthetic Methods)CEepoxide opening
  246357. b-hydroxy ester
  246358. lithium ammonia reduction
  246359. epoxy esterI
  246360. This method is suitable for aliphatic glycidic acid esters which do not give diastereomers upon ring opening.  Previous reagents used [e.g. NaTeH, SmI2/HMPT, and (PhSe)2/NaBH4]  although efficient, are expensive and/or toxic.M
  246361. 20997N
  246362. 2/28/96W
  246363. 1990X
  246364. 897-899
  246365. Solladie-Cavallo, A.B
  246366. Tet. Lett.C~reduction
  246367. DIBAL
  246368. chelation control
  246369. zinc chloride
  246370. chiral sulfoxide
  246371. b-hydroxy sulfoxide
  246372. b-keto sulfoxide
  246373. 1,3-asymmetric inductionI
  246374. K<The absence of ZnCl2 causes up to 0% reversal of selectivityM
  246375. 20998N
  246376. 2/28/96W
  246377. 1990X    6649-6652Y
  246378. Adams, C. M.
  246379. Schemenaur, J. E.B.Synth. Commun.  (Journal of Synthetic Methods)Cfselective reduction
  246380. aldehyde
  246381. ketone
  246382. acid chloride
  246383. zinc copper couple
  246384. titanium (0)
  246385. tributyltin hydride
  246386. KSAcyl chlorides are unaffected.  Generation of Ti(0) from Cp2TiCl2 / Zn(Cu) / Bu3SnHM
  246387. 20999N
  246388. 2/28/96W
  246389. 1990X    2359-2364Y
  246390. Solodin, I.
  246391. JCS C.C.
  246392. C_reduction
  246393. dimethylphenylsilane
  246394. silane
  246395. a-hydroxyamide
  246396. 4-imidazolidone
  246397. cesium fluoride
  246398. 18-crown-6I
  246399. KMProducts are easily converted to a-hydroxy amides.  Also reduction with NaBH4M
  246400. 21000N
  246401. 2/28/96W
  246402. 1990X    1321-1322
  246403. Cho, B. T.
  246404. Chun, Y. S.
  246405. B J. Chem. Soc.  Perkin Trans. I  C\asymmetric reduction
  246406. Itsuno's reagent
  246407. secondary amine
  246408. ketimine
  246409. chiral oxazaborolidine
  246410. boraneI
  246411. K+Reduction of ketimine with Itsuno's reagentM
  246412. 21001N
  246413. 2/28/96W
  246414. 1990X    3200-3201
  246415. Schummer, D.
  246416. Holfe, G.B'Synlett  (Journal of Synthetic Methods)Csthiocarbonic acid ester
  246417. deoxygenation
  246418. secondary alcohol
  246419. tris(trimethylsilyl)silane
  246420. tributyltin hydride
  246421. free radicalI
  246422. KnTris(trimethylsilyl)silane is a relatively safe alternative to Bu3SnH due to the absence of toxic by-products.M
  246423. 21002N
  246424. 2/28/96W
  246425. 1990X
  246426. 705-706
  246427. Huang, X.
  246428. Pi, J-H.B.Synth. Commun.  (Journal of Synthetic Methods)CCb-ketosulfone
  246429. sodium hydrogen telluride
  246430. 18-crown-6
  246431. ketone
  246432. reductionI
  246433. 21003N
  246434. 2/28/96W
  246435. X    2297-2300Y
  246436. Lee, S-B.
  246437. Takata, T.
  246438. Endo, T.B-Chem. Letters  (Journal of Synthetic Methods)C
  246439. protecting group
  246440. acetal
  246441. epoxide
  246442. aldehyde
  246443. n-(4-methoxy-benzyl)-2-cyanopyridinium hexafluoroantimonate
  246444. antimony
  246445. 1,3-dioxolane
  246446. lactone
  246447. ketalsI
  246448. Catalyst is easy to handle due to its good stability in air and moisture.  Also formation of spiroorthocarboxylic ar spiroorthocarbonic acid esters from lactones or cylic carbonic acid esters.M
  246449. 21004N
  246450. 2/28/96W
  246451. 1990X    2019-2022
  246452. Racherla, U. S.
  246453. Brown, H. C.B
  246454. JOCCeallyl boration
  246455. boron
  246456. aldehyde
  246457. condensation
  246458. Grignard reagent
  246459. magnesium salt
  246460. ate complex
  246461. allyl alcohol
  246462. Under these new salt free conditions the reaction is instantaneous even at -100
  246463. C.  The ability to run the reactions at this temperature is the reason for the increased enantioselectivity.  When the reaction is run in the presence of Mg salts the reaction time is much longer 1-3 hrs at -78
  246464. C.  This is due to the formation of an ate complex of boron with the Mg salts which is not reactive in the allylboration reaction.  
  246465. 21005N
  246466. 2/28/96V
  246467. Chiral Synthesis via Organoboranes. 27. Remarkably Rapid and Exceptionally Enantioselective (Approaching 100% ee) Allylboration of Representative Aldehydes at -100
  246468. C under New Salt Free ConditionsW
  246469. 1991X
  246470. 401-404Y
  246471. A&Keck, G. E.
  246472. Andrus, M. B.
  246473. Romer, D. R.B
  246474. JOCCireduction
  246475. DIBAL
  246476. magnesium bromide etherate
  246477. chelation control
  246478. ester
  246479. aldehyde
  246480. benzyl group
  246481. protecting groupI
  246482. Selective activation of the C1 ester via bidentate complexation of the C1 carbonyl and the C2 benzyloxy group.  The C1 ester can also be selectively reduced to the alcohol utilizing 2 eq. DIBAL.  Examples are shown using the aldehyde formed in other chelation-controlled addition reactions using allyl and vinyl metals, giving high levels of syn selectivity.  The benzyl group is put on using the benzyltrichloroimidate and TFA in 68% yield.  
  246483. 21006N
  246484. 2/28/96V{A Useful New Enantiomerically Pure Synthon from Malic Acid:  Chelation-Controlled Activation as a Route to RegioselectivityW
  246485. 1991X
  246486. 417-420Y
  246487. A2Boyd, S. A.
  246488. Mantei, R. A.
  246489. Hsiao, C-N.
  246490. Baker, W. R.B
  246491. JOCCJaldol
  246492. boron enolate
  246493. deoxygenation
  246494. thiocarbamate
  246495. xanthate
  246496. peptide coupling
  246497. Key step in both of the two syntheses is shown below.  Target compound is deoxygenated at the free hydroxyl, is an n-butyl amide where the chiral auxilliary is, and is deprotected (acetonide and Boc groups).  Remainder of the first synthesis involves deoxygenation of a thiocarbamate (Barton, McCombie), removal of the chiral auxilliary to form the carboxylic acid.  Amide formation followed by deprotection leads to the target.  The second synthesis involves attack of n-butylamine to form theBr n-butyl amide followed by deoxygenation of a xanthate to produce a common intermediate with the first synthesis. 
  246498. 21007N
  246499. 2/28/96V@Stereoselective Synthesis of Hydroxyethylene Dipeptide IsosteresW
  246500. 1991X
  246501. 438-442Y
  246502. Corey, E. J.
  246503. Link, J. O.B
  246504. JOCCHreduction
  246505. boron
  246506. oxazaborolidine
  246507. protecting group
  246508. alcohol
  246509. ketoneI
  246510. Enantioselective reduction using the R-oxazaborolidine.  Synthesis also involves removal of a secondary TES and aromatic TBS using KF/HCl in MeOH.
  246511. 21008N
  246512. 2/28/96VaA Catalytic Enantioselective synthesis of Denopamine, A Useful Drug for Congestive Heart Failure
  246513. 1991X
  246514. 442-444Y
  246515. Back, T. G.
  246516. Krishna, M. V.B
  246517. JOCCMselenosulfonation
  246518. selenium
  246519. sulfur
  246520. propargyl alcohol
  246521. epoxidation
  246522. MCPBA
  246523. epoxideI
  246524. 21009N
  246525. 2/28/96Vosynthesis of Castasterone and Formal synthesis of Brassinolide from Stigmasterol via Selenosulfonation ApproachW
  246526. 1991X
  246527. 454-457Y
  246528. A Ibuka, T.
  246529. Fujii, N.
  246530. Yamamoto, Y.B-Angew. Chem. Int. Ed. Engl. (Chem Highlights)C=mesylate
  246531. cyano cuprate
  246532. a,b-unsaturated ester
  246533. SN2' alkylation
  246534. 21010N
  246535. 2/28/96W
  246536. 1990X
  246537. Kato, N.
  246538. Takeshita, H.B(Bull. Chem. Soc. Japan (Chem Highlights)C=ene reaction
  246539. cyclization
  246540. Lewis acid
  246541. tin tetrachloride
  246542. thermalI
  246543. 21011N
  246544. 2/28/96W
  246545. 1990X
  246546. 1729Y
  246547. A'Homma, K.
  246548. Takenoshita, H.
  246549. Mukaiyama, T.B(Bull. Chem. Soc. Japan (Chem Highlights)CJsilyl ketene acetal
  246550. reduction
  246551. triethylsilane
  246552. antimony
  246553. Lewis acid 
  246554. oxonium
  246555. 21012N
  246556. 2/28/96
  246557. 1990X
  246558. 18948Y
  246559. Soai, K.
  246560. Niwa, S.
  246561. Hatanaka, T.
  246562. B(Bull. Chem. Soc. Japan (Chem Highlights)C3diethylzinc addition
  246563. alkylation
  246564. aldehyde
  246565. amino acidI
  246566. K;various amino acids were employed; 37-65% yields, 74-88% deM
  246567. 21013N
  246568. 2/28/96W
  246569. 1990X
  246570. 2129Y
  246571. A"Danishefsky, S. J.
  246572. Griffith, D. A.B$J. Am. Chem. Soc.  (Chem Highlights)C*iodofunctionalization
  246573. glycosylation
  246574. iodineI
  246575. 21014N
  246576. 2/28/96W
  246577. 1990X
  246578. 5811Y
  246579. Stork, G.
  246580. Zhao, K.B$J. Am. Chem. Soc.  (Chem Highlights)C"ester enolates
  246581. epoxide
  246582. alkylation
  246583. KTkey step towards the syntheses of (-)-Histrionicotoxin 235A and (-)-HistrionicotoxinM
  246584. 21015N
  246585. 2/28/96W
  246586. 1990X
  246587. 5875Y
  246588. Achiwa, K.
  246589. B$J. Am. Chem. Soc.  (Chem Highlights)C5hydrogenation
  246590. reduction
  246591. ketone
  246592. rhodium catalyst
  246593. MCCPMI
  246594. 21016N
  246595. 2/28/96W
  246596. 1990X
  246597. 5876Y
  246598. A Yamada, J.
  246599. Abe, H.
  246600. Yamamoto, Y.
  246601. B$J. Am. Chem. Soc.  (Chem Highlights)
  246602. Cvorgano lead reagent
  246603. chelation control
  246604. Lewis acid
  246605. aldol condensation 
  246606. titanium tetrachloride
  246607. boron trifluoride etherateI
  246608. 13 examples, 28-95% yield, diastereomeric ratio: 95:5- >99:1 for syn preference
  246609.                                                                                      39:61 - 11:89 for anti preferenceM
  246610. 21017N
  246611. 2/28/96W
  246612. 1990X
  246613. 6118Y
  246614. Knochel, P.
  246615. Rao, S. A.
  246616. B$J. Am. Chem. Soc.  (Chem Highlights)C;cuprate
  246617. zinc copper reagent
  246618. aldol condensation
  246619. vinyl copperI
  246620. 21018N
  246621. 2/28/96W
  246622. 1990X
  246623. 6146Y
  246624. Nicolaou, K. C.
  246625. B$J. Am. Chem. Soc.  (Chem Highlights)C?thiono lactone
  246626. alkylation
  246627. reduction
  246628. tributyltin hydride
  246629. radicalI
  246630. 21019N
  246631. 2/28/96W
  246632. 1990X
  246633. 6263Y
  246634. S. L. SchreiberB
  246635. JACSC7Samarium Iodide
  246636. Reductive Acylation
  246637. Anti-1,3-diol esterI
  246638. 21020N
  246639. 2/28/96VLTotal Synthesis of (-)-Rapamycin Using an Evans-Tishchenko Fragment CouplingW
  246640. 1993X
  246641. 7906Y
  246642. A. G. MeyersB
  246643. C4Allene Synthesis
  246644. Propargyl Mesylate
  246645. Copper enolate
  246646. 21021N
  246647. 2/28/96VQSynthesis of rac -7,8-Epoxy-4-basmen-6-one by a Transannular Cyclization StrategyW
  246648. 1993X
  246649. 7926Y
  246650. Roush, W. R.B$J. Am. Chem. Soc.  (Chem Highlights)C0crotylboronate
  246651. boron
  246652. aldol condensation
  246653. aldehydeI
  246654. K?yields 80-94%  diastereomeric ratio greater than 93:7, 62-88%eeM
  246655. 21022N
  246656. 2/28/96W
  246657. 1990X
  246658. 6339Y
  246659. A&Roush, W. R.
  246660. Palkowitz, A. D.
  246661. Ando, K.B$J. Am. Chem. Soc.  (Chem Highlights)C/crotylboronate
  246662. boranes
  246663. boron
  246664. aldol condensationI
  246665. 21023N
  246666. 2/28/96W
  246667. 1990X
  246668. 6348Y
  246669. A!Mudryk, B.
  246670. Shook, C. A.
  246671. Cohen, T.B$J. Am. Chem. Soc.  (Chem Highlights)C(spiroketal
  246672. cerium alkoxide
  246673. alkyl cerium
  246674. 21024N
  246675. 2/28/96W
  246676. 1990X
  246677. 6389 Y
  246678. Petasis, N A.
  246679. Bzowej, E. I.B$J. Am. Chem. Soc.  (Chem Highlights)CCmethylenation
  246680. lactone
  246681. ketone
  246682. terminal olefin
  246683. titanium
  246684. exo methyleneI
  246685. also methylenation of ketonesM
  246686. 21025N
  246687. 2/28/96W
  246688. 1990X
  246689. 6392Y
  246690. Corey, E. J.
  246691. Virgil, J. C.B$J. Am. Chem. Soc.  (Chem Highlights)C/cyclization
  246692. Micheal reaction
  246693. aldol condensationI
  246694. 21026N
  246695. 2/28/96W
  246696. 1990X
  246697. 6429Y
  246698. Evans, D. A.
  246699. Hoveyda, A. H.
  246700. B#J. Am. Chem. Soc. (Chem Highlights)C\reduction
  246701. acetylation
  246702. samarium iodide
  246703. reduction
  246704. b-hydroxy ketone
  246705. acetate
  246706. Tishchenko reactionI
  246707. K"intramolecular Tishchenko reactionM
  246708. 21027N
  246709. 2/28/96W
  246710. 1990X
  246711. 6447Y
  246712. A+Livingston, D. A.
  246713. Petre, J. E.
  246714. Bergh, C. L.B$J. Am. Chem. Soc.  (Chem Highlights)CGsilicon 
  246715. nitrile
  246716. silyl rearrangement
  246717. hydrolysis
  246718. acetate
  246719. a-chloro ketoneI
  246720. 21028N
  246721. 2/28/96W
  246722. 1990X
  246723. 6449Y
  246724. Davis, F. A.B$J. Am. Chem. Soc.  (Chem Highlights)CWchiral oxaziridine
  246725. camphorsulfonyl oxaziridine
  246726. camphor
  246727. a-hydroxylation
  246728. a-hydroxy ketoneI
  246729. 21029N
  246730. 2/28/96W
  246731. 1990X
  246732. 6679Y
  246733. A-Bakale, R. P.
  246734. Scialdone, M. A.
  246735. Johnson, C. R.B$J. Am. Chem. Soc.  (Chem Highlights)
  246736. Cetin elimination
  246737. b-keto stannanes
  246738. b-stannyl oximes
  246739. oxidation elimination
  246740. MCPBA
  246741. thionyl chloride
  246742. olefinI
  246743. K7also with b-stannyl oximes using SOCl2, pyridine at 0
  246744. 21030N
  246745. 2/28/96W
  246746. 1990X
  246747. 6729Y
  246748. Kocovsky, P.
  246749. B$J. Am. Chem. Soc.  (Chem Highlights)CMcyclopropane opening
  246750. thallium ion
  246751. rearrangement
  246752. lactol
  246753. a-hydroxy cyclopropaneI
  246754. 21031N
  246755. 2/28/96W
  246756. 1990X
  246757. 6735Y
  246758. Mikami, K.
  246759. Loh, T.-P.
  246760. Nakai, T.B$J. Am. Chem. Soc.  (Chem Highlights)CUvinyl silane
  246761. a-formyl ester
  246762. Lewis acid
  246763. tin tetrachloride
  246764. condensation
  246765. a-hydroxy esterI
  246766. 21032N
  246767. 2/28/96W
  246768. 1990X
  246769. 6737Y
  246770. Curran, D. P.
  246771. B$J. Am. Chem. Soc.  (Chem Highlights)CIradical cyclization
  246772. hexabutylditin
  246773. tributyltin hydride
  246774. camphor sultamI
  246775. 21033N
  246776. 2/28/96W
  246777. 1990X
  246778. 6738Y
  246779. Porter, N. A.
  246780. B$J. Am. Chem. Soc.  (Chem Highlights)CYfree radical addition
  246781. trans-2,5-dimethylpyrrolidine
  246782. tributyltin hydride
  246783. a-bromoamideI
  246784. 21034N
  246785. 2/28/96W
  246786. 1990X
  246787. 6740Y
  246788. McMurray, J. E.
  246789. Dushin R. G.
  246790. B#J Am. Chem. Soc.  (Chem Highlights)C
  246791. titanium carbonyl coupling
  246792. KVkey step in total synthesis of (
  246793. )-Isolobophytolide and (
  246794. )-Crassin (from cis lactone)M
  246795. 21035N
  246796. 2/28/96W
  246797. 1990X
  246798. 6942Y
  246799. A)Abelman, M. M.
  246800. Overman, L. E.
  246801. Tran, V. D.B$J. Am. Chem. Soc.  (Chem Highlights)C>intramolecular palladium catalyzed coupling
  246802. aryl iodide
  246803. alkeneI
  246804. KKkey step in the total synthesis of (
  246805. )-Tazettine and (
  246806. )-6a-EpipretazettineM
  246807. 21036N
  246808. 2/28/96W
  246809. 1990X
  246810. 6959Y
  246811. Evans, D. A.B$J. Am. Chem. Soc.  (Chem Highlights)C
  246812. CytovaricinI
  246813. 21037N
  246814. 2/28/96W
  246815. 1990X
  246816. 7001Y
  246817. Lipshutz, B. H.B%J. Am. Chem. Soc.  (Chem Highlights) C0urethane cyclization
  246818. decarboxylation
  246819. hydrolysis
  246820. 21038N
  246821. 2/28/96W
  246822. 1990X
  246823. 7032Y
  246824. Fukuyama, T.
  246825. Lin, S.-C.
  246826. Li, L.B$J. Am. Chem. Soc.  (Chem Highlights)C+reduction
  246827. thioester
  246828. aldehyde
  246829. triethylsilaneI
  246830. 21039N
  246831. 2/28/96W
  246832. 1990X
  246833. 7050Y
  246834. Dupoantier, A. J.
  246835. Masamune, S.B#J. Am. Chem. Soc. (Chem Highlights)C
  246836. Pimarolide methyl esterI
  246837. K#synthesis of pimarolide methylesterM
  246838. 21040N
  246839. 2/28/96W
  246840. 1990X
  246841. 7079Y
  246842. Arya, P.
  246843. Chan, T. H.B&J. C. S. Chem. Comm. (Chem Highlights)C}diphenylisopropoxylsilyl ether
  246844. protecting group
  246845. Lewis acid
  246846. titanium tetrachloride
  246847. acetylene
  246848. halo olefin
  246849. cyclic ether
  246850. aldehydeI
  246851. 21041N
  246852. 2/28/96W
  246853. 1990X
  246854. Mikami, K.
  246855. Nakai, T.
  246856. B'J. C. S. Chem. Comm.  (Chem Highlights)CWallylstannanes
  246857. aldol condensation
  246858. a-alkoxy aldehyde
  246859. chelation control
  246860. magnesium bromideI
  246861. K*10 examples 70-90% 93:7-3:99 erythro/threoM
  246862. 21042N
  246863. 2/28/96W
  246864. 1990X
  246865. Herscovici, J.
  246866. B*J. C. S. Perkin Trans 1 (Chem Highlights) C/alkylation
  246867. oxonium
  246868. tin tetrabromide
  246869. Lewis acid
  246870. 21043N
  246871. 2/28/96W
  246872. 1990X
  246873. A'Begley, M. J.
  246874. Fish, P. V.
  246875. Pattenden, G.B)J. C. S. Perkin Trans 1 (Chem Highlights)CBmCPBA oxidation
  246876. aluminum hydride
  246877. epoxide
  246878. MOM protecting group
  246879. pTSAI
  246880. 21044
  246881. 2/28/96W
  246882. 1990X
  246883. Konradi, A. W.
  246884. Pederson, S. F.B J. Org. Chem.  (Chem Highlights)C6aldehyde coupling
  246885. chiral carbonate
  246886. vanadium zinc saltsI
  246887. KA3 other examples  70-92% yield   diastereoselectivity 1:1 to 50:1M
  246888. 21045N
  246889. 2/28/96W
  246890. 1990X
  246891. 4497Y
  246892. Gong, B.
  246893. Lynn, D. G.B
  246894. J. Org. Chem. (Chem Highlights)Cdselective reduction 
  246895. dicarboxylic acid - lactone
  246896. amino acid
  246897. triethylborane
  246898. borane
  246899. hydrochloride saltI
  246900. 21046N
  246901. 2/28/96W
  246902. 1990X
  246903. 4763Y
  246904. Sato, T.
  246905. Otera, J.
  246906. Nozaki, H.B
  246907. J. Org. Chem. (Chem Highlights)C&THP removal
  246908. boron trifluoride etherateI
  246909. 15 other examples  70-97% yieldM
  246910. 21047N
  246911. 2/28/96W
  246912. 1990X
  246913. 4770Y
  246914. Cohen, T.
  246915. Doubleday, M. D.B
  246916. J. Org. Chem. (Chem Highlights)C
  246917. ketone
  246918. vinyl sulfide formation
  246919. montmorillonite
  246920. vinyl lithium
  246921. p,p'-di-tert-butylphenylide  (LDBB)
  246922. vinyl lithium - aldehyde couplingI
  246923. KY12 other examples 52-86% yield vinylsulfide formation, 68-92% yield for coupling reactionM
  246924. 21048
  246925. 2/28/96W
  246926. 1990X
  246927. 4784Y
  246928. Chou, T-S.
  246929. Knochel, P.B
  246930. J. Org. Chem. (Chem Highlights)C
  246931. a-acetoxy copper-zinc reagentsI
  246932. KR7 other examples, >85% yield, describes reactivity with a variety of electrophilesM
  246933. 21049N
  246934. 2/28/96W
  246935. 1990X
  246936. 4791Y
  246937. Eisch, J. J.
  246938. Galle, J. E.B
  246939. J. Org. Chem. (Chem Highlights)C
  246940. epoxide
  246941. silyl epoxideI
  246942. 14 other examples, 35-95% yieldM
  246943. 21050N
  246944. 2/28/96W
  246945. 1990X
  246946. 4835Y
  246947. A,Molander, G. A. 
  246948. Burkhardt, E. R.
  246949. Weinig, P.B J. Org. Chem.  (Chem Highlights)C)alkylation
  246950. organolithium
  246951. Yb(OTf)3
  246952. ketone
  246953. K/13 other examples : 53-99% yield, 82:18 - 200:1M
  246954. 21051N
  246955. 2/28/96W
  246956. 1990X
  246957. 4990Y
  246958. A"Dunn, P. J.
  246959. Haner, R.
  246960. Rapoport, H.B
  246961. J. Org. Chem. (Chem Highlights)CRester enolate
  246962. KHMDS
  246963. alkylation
  246964. benzyl iodide
  246965. 9-phenylfluoren-9-yl
  246966. amine protectionI
  246967. 21052N
  246968. 2/28/96W
  246969. 1990X
  246970. 5017Y
  246971. Martinelli, M. J.B J. Org. Chem.  (Chem Highlights)C%Diels-Alder reaction
  246972. chiral carbonateI
  246973. KC10 other examples of asymmetric Diels-Alder reaction : 75-99% yieldM
  246974. 21053N
  246975. 2/28/96W
  246976. 1990X
  246977. 5065Y
  246978. Roelens, S.B J. Org. Chem.  (Chem Highlights)CFdiol protection
  246979. dibutyltin oxide
  246980. benzoyl chloride
  246981. trimethylsilyl etherI
  246982. K3many examples: 30-95%;regioselectivity 95:5 - <1:99M
  246983. 21054N
  246984. 2/28/96W
  246985. 1990X
  246986. 5132Y
  246987. Evans, D. A.
  246988. Hoveyda, A. H.B J. Org. Chem. (Chem Highlights) I
  246989. K!many examples: 76-93%, 6:1 - 80:1M
  246990. 21055N
  246991. 2/28/96W
  246992. 1990X
  246993. 5190Y
  246994. A8Barrett, A. G. M.
  246995. Bezuidenhoudt, B. C. B.
  246996. Melcher, L. M.B
  246997. J. Org. Chem. (Chem Highlights)CDintramolecular iodo etherification
  246998. TBDPS deprotection
  246999. TBAF on silicaI
  247000. 21056N
  247001. 2/28/96W
  247002. 1990X
  247003. 5196Y
  247004. A    Padwa, A.B J. Org. Chem.  (Chem Highlights)C%diazo ketone coupling
  247005. aldehyde
  247006. SnCl2
  247007. 13 other examples 0-90%M
  247008. 21057N
  247009. 2/28/96W
  247010. 1990X
  247011. 5297Y
  247012. Yamamoto, Y.
  247013. Asao, N.B
  247014. J. Org. Chem. (Chem Highlights)
  247015. CWmesylate displacement with retention of configuration
  247016. azide
  247017. sodium azide/copper iodide
  247018. K'5 other examples 50-90%;   76:24 - 91:9M
  247019. 21058N
  247020. 2/28/96W
  247021. 1990X
  247022. 5303Y
  247023. A)Lautens, M.
  247024. Abd-El-Aziz, A. S. 
  247025. Lough, A.B J. Org. Chem.  (Chem Highlights)C
  247026. dihydropyran ring opening
  247027. nBuLiI
  247028. 8 other examples 72-92%M
  247029. 21059N
  247030. 2/28/96W
  247031. 1990X
  247032. 5305Y
  247033. Kobayashi, Y.
  247034. Sato, F.B J. Org. Chem.  (Chem Highlights)CPhydroboration
  247035. palladium catalyzed coupling
  247036. vinyl iodide
  247037. disiamylborane
  247038. acetyleneI
  247039. 21060N
  247040. 2/28/96W
  247041. 1990X
  247042. 5324Y
  247043. A#Bergdahl, M.
  247044. Nilsson, M.
  247045. Olsson, T.B&J. Organomet. Chem.  (Chem Highlights)CTconjugate addition
  247046. cuprate
  247047. LAH reduction
  247048. ester - alcohol
  247049. chiral auxilliary - camphorI
  247050. 21061N
  247051. 2/28/96W
  247052. 1990X
  247053. Bringmann, G.B$Liebigs Ann. Chem. (Chem Highlights)CDimine formation / reduction
  247054. Raney nickel
  247055. chiral amine
  247056. hydrogenolysisI
  247057. K#12 examples 45-75% yield, 92-98% eeM
  247058. 21062N
  247059. 2/28/96W
  247060. 1990X
  247061. Bianchini, C.B"Organometallics  (Chem Highlights)C trans hydrogenation of acetyleneI
  247062. 21063N
  247063. 2/28/96W
  247064. 1990X
  247065. 2283Y
  247066. Huang, Z. -Z.
  247067. Zhou, X. -J.B
  247068. Synthesis (Chem Highlights)CXbromoethyl ester - acid
  247069. selenium
  247070. sodium hydrogen telluride
  247071. sodium borohydride
  247072. reduction
  247073. 6 other examples 87-95%M
  247074. 21064N
  247075. 2/28/96W
  247076. 1889X
  247077. Brown, H. C.
  247078. Kandad, R. S.B
  247079. Tetrahedron (Chem Highlights)C'chiral crotyl borane
  247080. aldol condensationI
  247081. K(E olefin gives corresponding anti isomerM
  247082. 21065N
  247083. 2/28/96W
  247084. 1990X
  247085. 4457Y
  247086. Brown, H. C.
  247087. Kandad, R. S.B
  247088. Tetrahedron  (Chem Highlights)CJaldol condensation
  247089. chiral allyl boronate
  247090. isopinocampheyl borane
  247091. Ipc boraneI
  247092. K(5 other examples 60-65% yield, 90-98% eeM
  247093. 21066N
  247094. 2/28/96W
  247095. 1990X
  247096. 4463Y
  247097. Takle, A.
  247098. Kocienski, P.B
  247099. Tetrahedron  (Chem Highlights)C
  247100. spiroketal formationI
  247101. K#key step in synthesis of Lacrimin AM
  247102. 21067N
  247103. 2/28/96W
  247104. 1990X
  247105. 4503 Y
  247106. A!Asao, N.
  247107. Uyehara, T.
  247108. Yamamoto, Y.
  247109. TetrahedronC ester enolate aldol condensationI
  247110. 7 other examples 39-72% yieldsM
  247111. 21068N
  247112. 2/28/96W
  247113. 1990X
  247114. 4503Y
  247115. A"Ishihara, K.
  247116. Mori, A.
  247117. Yamamoto, H.B
  247118. Tetrahedron  (Chem Highlights)C4hydride opening of cyclic ether
  247119. DIBAL
  247120. triethylsilaneI
  247121. 21069N
  247122. 2/28/96W
  247123. 1990X
  247124. 4595Y
  247125. A$Mukaiyama, T.
  247126. Kobayashi, S.
  247127. Sano, T.B
  247128. Tetrahedron  (Chem Highlights)CVsilyl enol ether aldol condensation
  247129. Sn(OTf)2 nBu3SnF
  247130. chiral amine base
  247131. b-hydroxy esterI
  247132. K&other examples 51-79% yield, 89-98% eeM
  247133. 21070N
  247134. 2/28/96W
  247135. 1990X
  247136. 4653Y
  247137. Fox, D. N. A.
  247138. Gallagher, T.B
  247139. Tetrahedron  (Chem Highlights)C6amino cyclization
  247140. silver ion catalyzed
  247141. silver triflateI
  247142. K(12 other examples 63-90% yield; 5-80% deM
  247143. 21071N
  247144. 2/28/96W
  247145. 1990X
  247146. 4697Y
  247147. Friesen, R. W.B$Tetrehedron Lett.  (Chem Highlights)C8iodo amination
  247148. cyclization
  247149. carbamate
  247150. vinyl iodide
  247151. alleneI
  247152. K<5 other examples  50-80% overall yields; syn:anti 10:1->99:1M
  247153. 21072N
  247154. 2/28/96W
  247155. 1990X
  247156. 4249Y
  247157. Sengupta, S.
  247158. Snieckus, V.B$Tetrahedron Lett.  (Chem Highlights)CParomatic directed metalation
  247159. SEM directed
  247160. silylation
  247161. aldol reaction
  247162. desilylationI
  247163. K%10 examples with aryl systems  52-87%M
  247164. 21073N
  247165. 2/28/96W
  247166. 1990X
  247167. 4267Y
  247168. Majid, T. N.
  247169. Knochel, P.B$Tetrahedron Lett.  (Chem Highlights)C)Zinc copper reagent
  247170. allyl iodide
  247171. couplingI
  247172. K 14 other examples  61-93% yieldsM
  247173. 21074N
  247174. 2/28/96W
  247175. 1990X
  247176. 4413Y
  247177. Malacria, M.B$Tetrahedron Lett.  (Chem Highlights)C>free radical cyclization
  247178. silyl oxidation
  247179. a-bromo silyl alcoholI
  247180.     K34 other examples 65-89% yield; ratios 42:58 - 100:0M
  247181. 21075N
  247182. 2/28/96W
  247183. 1990X
  247184. 4445Y
  247185. Sato, F.B$Tetrahedron Lett.  (Chem Highlights)C'zinc copper reagent
  247186. conjugate addition I
  247187. 5 other examples  75-95% yieldM
  247188. 21076N
  247189. 2/28/96W
  247190. 1990X
  247191. 4481Y
  247192. A.Yadav, J. S.
  247193. Deshpande, P. K.
  247194. Sharma, G. V. M.B$Tetrahedron Lett.  (Chem Highlights)C7a-chloro epoxide
  247195. chlorovinyl alcohol
  247196. propargyl alcohol
  247197. KP6 other examples  41-87% for chlorovinyl alcohols, 19-77% for propargyl alcoholsM
  247198. 21077N
  247199. 2/28/96W
  247200. 1990X
  247201. 4495Y
  247202. Lipshutz, B.B$Tetrahedron Lett.  (Chem Highlights)C8allyl tin
  247203. allyl lithium
  247204. allyl cuprate
  247205. conjugate additionI
  247206. 7 other examples 72-99% yieldsM
  247207. 21078N
  247208. 2/28/96W
  247209. 1990X
  247210. 4539Y
  247211. Soderquist, J. A.B$Tetrahedron Lett.  (Chem Highlights)CHacyl silane
  247212. boronate
  247213. isopinocampheyl borane  
  247214. Ipc borane
  247215. a-silyl alcoholI
  247216. K(5 other examples, 0-64% yields, 0-98% eeM
  247217. 21079N
  247218. 2/28/96W
  247219. 1990X
  247220. 4677Y
  247221. Suzuki, T.
  247222. Sato, O.
  247223. Hirama, M.B$Tetrahedron Lett.  (Chem Highlights)CQdeprotection of TBDPS ether
  247224. silyl ether
  247225. epoxide opening
  247226. tetrahydropyran
  247227. palladiumI
  247228. Khtrans epoxide: 90% yield, 1/2 = >99/1
  247229. cis epoxide: 89% yield, 1/2 = 2/98
  247230. 8 other examples, 45-90% yieldsM
  247231. 21080N
  247232. 2/28/96W
  247233. 1990X
  247234. 4747Y
  247235. Fang, C.
  247236. Suemune, H.
  247237. Sakai, K.B$Tetrahedron Lett.  (Chem Highlights)
  247238. Coconjugate addition
  247239. cuprate
  247240. LAH reduction of ester
  247241. intramolecular trapping by alkyl chloride
  247242. chiral cyclopentaneI
  247243. 16 other examples 15-91% yieldM
  247244. 21081N
  247245. 2/28/96W
  247246. 1990X
  247247. 4751Y
  247248. Momose, T.
  247249. B#Tetrahedron Lett. (Chem Highlights)C_chiral piperidine
  247250. intramolecular cyclization
  247251. chiral amine
  247252. hydrogenation
  247253. Boc protection of amineI
  247254. K+key step towards synthesis of (+)-yohimbineM
  247255. 21082N
  247256. 2/28/96W
  247257. 1990X
  247258. 4755Y
  247259. Shim, S. C.
  247260. Kang, H.-Y.B$Tetrahedron Lett.  (Chem Highlights)C,samarium iodide cyclization
  247261. acetylene
  247262. ketoneI
  247263. 23 other examples, 0-75% yieldM
  247264. 21083N
  247265. 2/28/96W
  247266. 1990X
  247267. 4765Y
  247268. Anastasiou, D.
  247269. Jackson, W. R.B$Tetrahedron Lett.  (Chem Highlights)COcarbonyl insertion
  247270. rhodium catalyst
  247271. olefinic amine
  247272. lactam formation
  247273. cyclizationI
  247274. 4 other examples, 83-91% yieldsM
  247275. 21084N
  247276. 2/28/96W
  247277. 1990X
  247278. 4795Y
  247279. Godfrey, A. G.
  247280. Ganem, B.B$Tetrahedron Lett.  (Chem Highlights)C&allyl bromide
  247281. allyl aldehyde
  247282. oxidationI
  247283. 8 other examplesM
  247284. 21085N
  247285. 2/28/96W
  247286. 1990X
  247287. 4825Y
  247288. A2Laszlo, P.
  247289. Montauflier, M.-T.
  247290. Randriamahefa, S. L.B$Tetrahedron Lett.  (Chem Highlights)Cdconjugate addition
  247291. b-ketoester to unsaturated ketone
  247292. nickel bromide on clay support
  247293. iron trichlorideI
  247294. 7 other examplesM
  247295. 21086N
  247296. 2/28/96W
  247297. 1990X
  247298. 4867Y
  247299. A'Delbecq, P.
  247300. Celerier, J.-P.
  247301. Lhommet, G.B$Tetrahedron Lett.  (Chem Highlights)C+decarbomethoxylation
  247302. b-ketoester
  247303. boric acidI
  247304. 8 other examplesM
  247305. 21087N
  247306. 2/28/96W
  247307. 1990X
  247308. 4873Y
  247309. Tamaru, Y.
  247310. B$Tetrahedron Lett.  (Chem Highlights)CDcarbamate formation
  247311. acetylenic carbamate
  247312. intramolecular cyclization
  247313. 20 other examplesM
  247314. 21088N
  247315. 2/28/96W
  247316. 1990X
  247317. 4887Y
  247318. A)Soderquist, J. A.
  247319. Santiago, B.
  247320. Rivera, I.B#Tetrahedron Lett. (Chem Highlights)C9vinyl bromide
  247321. allyl silane
  247322. palladium
  247323. bicyclo boron silaneI
  247324. 9 other examples >70% yieldM
  247325. 21089N
  247326. 2/28/96W
  247327. 1990X
  247328. 4981Y
  247329. Holmquist, C. R.
  247330. Roskamp, E. J.
  247331. B$Tetrahedron Lett.  (Chem Highlights)CHozonolysis
  247332. diazoester coupling to aldehyde
  247333. Lewis acid
  247334. SnCl2
  247335. b-ketoester I
  247336. 11 other examples 45-85%M
  247337. 21090N
  247338. 2/28/96W
  247339. 1990X
  247340. 4991Y
  247341. Bolm, C.
  247342. Ewald, M.
  247343. B$Tetrahedron Lett.  (Chem Highlights)Cgdiethylzinc addition
  247344. conjugate addition
  247345. a,b-unsaturated ketone
  247346. nickel catalyst
  247347. chiral pyridine catalystI
  247348. K"2 other examples, 68-76%, 2-74% eeM
  247349. 21091N
  247350. 2/28/96W
  247351. 1990X
  247352. 5011Y
  247353. Kamimura, A.
  247354. Marumo, S.B$Tetrahedron Lett.  (Chem Highlights)CUsilyl enol ether
  247355. Lewis acid
  247356. titanium tetrachloride
  247357. chiral aldehyde
  247358. aldol condensationI
  247359. K[syn/anti ratio dependent on Lewis acid
  247360. 15 other examples, >70% yield, syn/anti 97:3 to 2:98M
  247361. 21092N
  247362. 2/28/96W
  247363. 1990X
  247364. 50503Y
  247365. A*Kirwan, J. N.
  247366. Roberts, B. P.
  247367. Willis, C. R.B$Tetrahedron Lett.  (Chem Highlights)C,deoxygenation
  247368. xanthate
  247369. triethylsilane
  247370. thiol
  247371. 15 other examples, >60%M
  247372. 21093N
  247373. 2/28/96W
  247374. 1990X
  247375. 5093Y
  247376. Soderquist, J. A.
  247377. Santiago, B.
  247378. B$Tetrahedron Lett.  (Chem Highlights)C5acetylenic silane
  247379. hydroboration
  247380. reduction
  247381. vinylsilaneI
  247382. K.6 other examples, 60-76%, >99% isomeric purityM
  247383. 21094N
  247384. 2/28/96W
  247385. 1990X
  247386. 5113Y
  247387. Echavarren, A. M.B$Tetrahedron Lett.  (Chem Highlights)C<aryl triflate coupling
  247388. vinyl stannane
  247389. Palladium CouplingI
  247390. 9 other examples, 70-100%M
  247391. 21095N
  247392. 2/28/96W
  247393. 1990X
  247394. 5189Y
  247395. Wasserman, H. H. 
  247396. Vu, C. B.B$Tetrahedron Lett.  (Chem Highlights)CGphosphorus ylide condensation
  247397. acid chloride
  247398. oxone oxidation
  247399. diketoesterI
  247400. K44 other examples, 1st step; 86-96%, 2nd step; 71-86%M
  247401. 21096N
  247402. 2/28/96W
  247403. 1990X
  247404. 5205 Y
  247405. A    Kamal, A.B
  247406. Heterocycles (Chem Highlights)I
  247407. review: 33 refsM
  247408. 21097N
  247409. 2/28/96VBRecent Advances in The Synthetic Uses of Chlorocarbonyl IsocyanateW
  247410. 1990X
  247411. 1357Y
  247412. Oishi, T.
  247413. Nakata, T.B
  247414. Synthesis  (Chem Highlights)I
  247415. review: 49 refs.M
  247416. 21098N
  247417. 2/28/96V7New Aspects of Stereoselective Synthesis of 1,3-PolyolsW
  247418. 1990X
  247419. Ward, R. S.B
  247420. Tetrahedron  (Chem Highlights)I
  247421. review: 23 refs.M
  247422. 21099N
  247423. 2/28/96V
  247424. Asymmetric Synthesis of LignansW
  247425. 1990X
  247426. 5029Y
  247427. A"Junjappa, H.
  247428. Ila, H.
  247429. Asokan, C. V.B
  247430. Tetrahedron  (Chem Highlights)I
  247431. review: 225 refs.M
  247432. 21100N
  247433. 2/28/96VTa-Oxoketene -S,S -N,S and -N,N-Acetals: Versatile Intermediates in Organic SynthesisW
  247434. 1990X
  247435. 5423Y
  247436. Okamoto, K.
  247437. Goto, T.B
  247438. Tetrahedron (Chem Highlights)I
  247439. review: 134 refs.M
  247440. 21101N
  247441. 2/28/96V
  247442. Glycosidation of Sialic AcidW
  247443. 1990X
  247444. 5835Y
  247445. Alexakis, A.
  247446. Mangeney, P.B(Tetrahedron Asymmetry  (Chem Highlights)I
  247447. review: 170 refs.M
  247448. 21102N
  247449. 2/28/96V'Chiral Acetals in Asymmetric Synthesis
  247450. 1990X
  247451. A$Jalander, L.
  247452. Oksanen, L.
  247453. Rosling, A.B,Acta Chem. Scand., Ser. B  (Chem Highlights)C0vinyl tosylate
  247454. Grignard reagent
  247455. cuprate
  247456. couplingI
  247457. K+16 other examples 68-82% yields, 89:11-98:2M
  247458. 21103N
  247459. 2/28/96W
  247460. 1990X
  247461. Jager, J.
  247462. Hummer, W.
  247463. B.Angew. Chem. Int. Ed. Engl.  (Chem Highlights)C?palladium carbonylation reaction
  247464. carbamate cyclization
  247465. lactone I
  247466. one other example 58%M
  247467. 21104N
  247468. 2/28/96W
  247469. 1990X
  247470. 1171Y
  247471. A3Bumagin, N. A.
  247472. Andryukhova, N. P.
  247473. Beletskaya, I. P.B(Bull. Acad. Sci. USSR  (Chem Highlights)C=aryl iodide
  247474. palladium catalyzed coupling
  247475. a,b-unsaturated acidI
  247476. 3 other examples  95-98%M
  247477. 21105N
  247478. 2/28/96W
  247479. 1988X
  247480. 1285Y
  247481. Smit, V. A.B(Bull. Acad. Sci. USSR  (Chem Highlights)CMPausand Khand cyclization
  247482. cobalt protected acetylene
  247483. carbonylation
  247484. silica gelI
  247485. 11 other examples 43-92% yieldM
  247486. 21106N
  247487. 2/28/96W
  247488. 1988X
  247489. 2526Y
  247490. Sviridov, A. F.B(Bull. Acad. Sci. USSR  (Chem Highlights)C
  247491. erythronolide AI
  247492. #KDtotal synthesis of erythronolide A (61 steps with 0.28% total yield)M
  247493. 21107N
  247494. 2/28/96W
  247495. 1990X
  247496. Sviridov, A. F.B(Bull. Acad. Sci. USSR  (Chem Highlights)I
  247497. $K1key intermediate for synthesis of erythronolide BM
  247498. 21108N
  247499. 2/28/96W
  247500. 1989X
  247501. Mukaiyama, T.B(Bull. Chem. Soc. Jpn.  (Chem Highlights)Cbconjugate addition
  247502. silyl enol ether
  247503. Lewis acid catalysis
  247504. trityl perchlorate
  247505. a,b-unsaturated ketoneI
  247506. 13 other examples 62-100% yieldM
  247507. 21109N
  247508. 2/28/96W
  247509. 1990X
  247510. 2687Y
  247511. Kanemasa, S.B(Bull. Chem. Soc. Jpn.  (Chem Highlights)C;pyrollidine
  247512. cycloaddition
  247513. a,b-unsaturated ester
  247514. imine esterI
  247515. 21110N
  247516. 2/28/96W
  247517. 1990X
  247518. 2857Y
  247519. Mukaiyama, T.B(Bull. Chem. Soc. Jpn.  (Chem Highlights)C/dimethyl acetal
  247520. a-cyano methylether
  247521. TMSCN
  247522. NiCl2I
  247523. 21111N
  247524. 2/28/96W
  247525. 1990X
  247526. 3123Y
  247527. A#Bayle, J. P.
  247528. Perez, F.
  247529. Courtieu, J.B'Bull. Soc. Chim. Fr.  (Chem Highlights)C2aryl aldehyde
  247530. oxidation
  247531. aryl acid
  247532. sodium chlorite
  247533. 28 examples 0-98% yieldM
  247534. 21112N
  247535. 2/28/96W
  247536. 1990X
  247537. Lowinger, T. B.
  247538. Weiler, L.B Can. J. Chem.  (Chem Highlights)CSvinyltin cyclization
  247539. epoxide opening
  247540. chloro bis(h5-cyclopentadienyl)titanium (III)
  247541. )K&one other example 86% yield, Z:E <98:2
  247542. 21113N
  247543. 2/28/96W
  247544. 1990X
  247545. 1636Y
  247546. A Gordon, D. M.
  247547. Danishefsky, S. J.B Carbohyd. Res. (Chem Highlights)CJdimethyldioxirane oxidation
  247548. epoxidation
  247549. nucleophilic epoxide opening
  247550. azideI
  247551. *K0six examples varying nucleophiles, yields 43-86%M
  247552. 21114N
  247553. 2/28/96W
  247554. 1990X
  247555. Adam, W.
  247556. Hadjiarapoglou, L.B
  247557. Chem. Ber.  (Chem Highlights)C&epoxidation
  247558. dimethyldioxirane
  247559. furanoneI
  247560. 5 other examples 97-100% yieldM
  247561. 21115N
  247562. 2/28/96W
  247563. 1990X
  247564. 2077Y
  247565. Hayashi, Y.
  247566. Narasaka, K.B
  247567. Chem. Lett.  (Chem Highlights)CB[2,2] cyclization
  247568. chiral acetal
  247569. acetylenic thioether
  247570. TiCl2(0-iPr)2I
  247571. 21116N
  247572. 2/28/96W
  247573. 1990X
  247574. 1295 
  247575. Hosokawa, T.
  247576. Murahashi, S.B
  247577. Chem. Lett.  (Chem Highlights)C7palladium catalyzed cyclization
  247578. lactol
  247579. olefinic alcoholI
  247580. -K(5 other examples 63-85% yield, 81-99% deM
  247581. 21117N
  247582. 2/28/96W
  247583. 1990X
  247584. Mukaiyama, T.B Chem. Lett.  (Chem Highlights)  C
  247585. epoxidation
  247586. oxygen
  247587. Ni(dmp)2I
  247588. 5 other examples 67-81% yieldM
  247589. 21118
  247590. 2/28/96W
  247591. 1990X
  247592. Kawanami, Y.
  247593. Katayama, K.B
  247594. Chem. Lett.  (Chem Highlights)C6Grignard addition
  247595. chiral a-keto amide
  247596. Lewis acid
  247597. TiCl4I
  247598. /K215 other examples 62-94% yields, ratios 24:76-95:5M
  247599. 21119N
  247600. 2/28/96W
  247601. 1990X
  247602. Soucek, M.
  247603. Urbam, J.
  247604. Saman, D.B+Coll. Czech, Chem. Comm.  (Chem Highlights)C(reduction
  247605. amino acid
  247606. amino alcohol
  247607. NaBH4I
  247608. 21120N
  247609. 2/28/96W
  247610. 1990X
  247611. Enders, D.
  247612. Nakai, S.B#Helv. Chem. Acta  (Chem Highlights)C^SAMP hydrazone
  247613. enolate
  247614. a-silylketone
  247615. L-Selectride reduction
  247616. silyl oxidation
  247617. trans diol
  247618. KF/H2O2I
  247619. 1K%7 other examples 90-98% ee, 95-98% deM
  247620. 21121N
  247621. 2/28/96W
  247622. 1990X
  247623. 1833Y
  247624. A    Iwata, C.B
  247625. Heterocycles  (Chem Highlights)C
  247626. halolactonization
  247627. TMSBrI
  247628. 2K68 more examples, 2 resulting in cis bromolactonizationM
  247629. 21122N
  247630. 2/28/96W
  247631. 1990X
  247632. Masamune, S.B$J. Am. Chem. Soc.  (Chem Highlights)C
  247633. synthesis of bryostatin 7I
  247634. 21123N
  247635. 2/28/96W
  247636. 1990X
  247637. 7407Y
  247638. Nicolaou, K. C.B$J. Am. Chem. Soc.  (Chem Highlights)Cwlithium acetylide
  247639. ketone alkylation
  247640. free radical deoxygenation
  247641. thiocarbonyldiimidazole
  247642. tributyltin hydride
  247643. Dynemicin A
  247644. synthesis of Dynemicin A modelM
  247645. 21124N
  247646. 2/28/96W
  247647. 1990X
  247648. 7416Y
  247649. Yamamoto, H.B$J. Am. Chem. Soc.  (Chem Highlights)C"HCHO
  247650. formaldehyde equivalent
  247651. 5KD5 more examples (61-92%).  HCHO
  247652. MAPH is a stable formaldehyde sourceM
  247653. 21125N
  247654. 2/28/96W
  247655. 1990X
  247656. 7422Y
  247657. Isaka, M.
  247658. Nakamura, E.B#J. Am. Chem. Soc. (Chem Highlights)C7alkylation
  247659. dimethylcuprate
  247660. acylation
  247661. acetal hydrolysis
  247662. 21126N
  247663. 2/28/96W
  247664. 1990X
  247665. 7428Y
  247666. Knochel, P.
  247667. B$J. Am. Chem. Soc.  (Chem Highlights)C;boron stabilized carbanion
  247668. zinc copper carbanion
  247669. alkylationI
  247670. 7KL14 more examples of new preparations of boron stabilized carbanions (63-95%)M
  247671. 21127N
  247672. 2/28/96W
  247673. 1990X
  247674. 7431Y
  247675. Linderman, R. J.B$J. Am. Chem. Soc.  (Chem Highlights)
  247676. CCsilyl enol ether
  247677. a-silyl ether
  247678. furanone
  247679. chromium trioxide oxidationI
  247680. 8KO5 more examples of furanone synthesis via an electrophilc capped carbonyl ylideM
  247681. 21128N
  247682. 2/28/96W
  247683. 1990X
  247684. 7438Y
  247685. A Lipshutz, B. H.
  247686. Ellsworth, E. L.B$J. Am. Chem. Soc.  (Chem Highlights)CUhydrozirconation
  247687. vinyl lithium
  247688. vinylcuprate
  247689. conjugate addition
  247690. a,b-unsaturated ketoneI
  247691. 9Kf8 more examples (71-100%)
  247692. see also K. A. Babiak, J. S. Ng, et al.  J. Am. Chem. Soc.  112, 7441 (1990)M
  247693. 21129N
  247694. 2/28/96W
  247695. 1990X
  247696. 7440Y
  247697. Seebach, D.B$J. Am. Chem. Soc.  (Chem Highlights)C,[3+3] cyclization
  247698. nitroallylic ester
  247699. enamineI
  247700. :K[many examples of stereoselective [3+3]-carbocyclization of nitroallylic esters and enaminesM
  247701. 21130N
  247702. 2/28/96W
  247703. 1990X
  247704. 7625Y
  247705. A#Maruoka, K.
  247706. Banno, H.
  247707. Yamamoto, H.
  247708. B$J. Am. Chem. Soc.  (Chem Highlights)CbClaisen rearrangement
  247709. acyl silane
  247710. vinyl silane
  247711. enol ether
  247712. chiral aluminum binap reagent
  247713. Lewis acidI
  247714. KG9 more examples of asymmetric Claisen rearrangement (22-99%, 14-93% ee)M
  247715. 21131N
  247716. 2/28/96W
  247717. 1990X
  247718. 7791Y
  247719. A'Utimoto, K.
  247720. Nakamura, A.
  247721. Matsubara, S.
  247722. B$J. Am. Chem. Soc.  (Chem Highlights)C"ketone alkylation
  247723. Lewis acid
  247724. YbCl3I
  247725. <K*23 other examples, yields 0-99%, de 12-98%M
  247726. 21132N
  247727. 2/28/96W
  247728. 1990X
  247729. 8189Y
  247730. Nicolaou, K. C.B#J. Am. Chem Soc.  (Chem Highlights)C
  247731. Calicheamicin
  247732. oligosaccharideI
  247733. <KCtotal synthesis of the oliogosaccharide fragment of Calicheamcin g1M
  247734. 21133N
  247735. 2/28/96W
  247736. 1990X
  247737. 8193 Y
  247738. Meyers, A. G.
  247739. Kukkola, P. J.
  247740. B$J. Am. Chem. Soc.  (Chem Highlights)C6hydrazone alkylation, hydrolysis
  247741. vinyl lithium
  247742. olefin
  247743. =K-6 other examples 77-90% yield, E/Z 1:1 - 20:1M
  247744. 21134N
  247745. 2/28/96W
  247746. 1990X
  247747. 8208Y
  247748. A"Magnus, P.
  247749. Stamford, A.
  247750. Ladlow, M.B$J. Am. Chem. Soc.  (Chem Highlights)C
  247751. vinblastineI
  247752. synthesis of VinblastineM
  247753. 21135N
  247754. 2/28/96W
  247755. 1990X
  247756. 8210Y
  247757. Evans, D. A.
  247758. B$J. Am. Chem. Soc.  (Chem Highlights)C(titanium enolate
  247759. alkylation
  247760. oxazolidine
  247761. >K*7 other examples 70-99% yields, 70->99% deM
  247762. 21136N
  247763. 2/28/96W
  247764. 1990X
  247765. 8215Y
  247766. A+Gyorkos, A. C.
  247767. Stille, J. K.
  247768. Hegedus, L. S.B$J. Am. Chem. Soc.  (Chem Highlights)CLpalladium catalyzed coupling
  247769. vinyl stannane
  247770. vinyl triflate
  247771. carbonylation
  247772. 21137N
  247773. 2/28/96V
  247774. Synthesis of JatrophoneW
  247775. 1990X
  247776. 8465Y
  247777. Wender, P. A.
  247778. Manly, C. J.
  247779. B$J. Am. Chem. Soc.  (Chem Highlights)C@lactone deprotonation
  247780. iodide elimination
  247781. a,b-unsaturated lactoneI
  247782. 21138N
  247783. 2/28/96W
  247784. 1990X
  247785. 8579Y
  247786. Negishi, E.-I.
  247787. B$J. Am. Chem. Soc.  (Chem Highlights)C=palladium catalyzed cyclization
  247788. vinyl iodide
  247789. steroid skeletonI
  247790. 2 other examples, >90% yieldM
  247791. 21139N
  247792. 2/28/96W
  247793. 1990X
  247794. 8590Y
  247795. White, J. D.
  247796. B$J. Am. Chem. Soc.  (Chem Highlights)C0aromatic coupling
  247797. trichloroethoxyester
  247798. VOF3I
  247799. BK"1 other example, 21% overall yieldM
  247800. 21140N
  247801. 2/28/96W
  247802. 1990X
  247803. 8595Y
  247804. Ranu, B. C.
  247805. Das, A. R.B'J. C. S. Chem. Comm.  (Chem Highlights)C+epoxide opening
  247806. zinc borohydride/silica gelI
  247807. CKQ7 other examples: 84-91%, generally >90% selectivity for less substituted alcoholM
  247808. 21141N
  247809. 2/28/96W
  247810. 1990X
  247811. Hayashi, M.
  247812. Matsuda, T.B'J. C. S. CHem. Comm.  (Chem Highlights)C2chiral silyl cyanation
  247813. aldehyde
  247814. Sharpless catalystI
  247815. DK#4 other examples: 89-92%, 73-81% eeM
  247816. 21142N
  247817. 2/28/96W
  247818. 1990X
  247819. A'Palomo, C.
  247820. Aizpurua, J. M.
  247821. Urchegui, R.B'J. C. S. Chem. Comm.  (Chem Highlights)CLsilyl cuprate
  247822. a,b-unsaturated ester
  247823. conjugate addition/cyclization
  247824. hydrazoneI
  247825. EK%key step in (
  247826. )-Thienamycin synthesisM
  247827. 21143N
  247828. 2/28/96W
  247829. 1990X
  247830. Ishibashi, H.
  247831. Ikeda, M.B'J. C. S. Chem. Comm.  (Chem Highlights)CKa-amide sulfone
  247832. aromatic coupling
  247833. a-amido sulfide
  247834. trifluoroacetic acid
  247835. TFAAI
  247836. FK.key step in (
  247837. )-Cephalotaxinel total synthesisM
  247838. 21144N
  247839. 2/28/96W
  247840. 1990X
  247841. Salazar, J. A.
  247842. B+J. C. S. Perkin Trans. 1  (Chem Highlights)C*phenyl selenation
  247843. b-selenylurethane
  247844. olefinI
  247845. many further examplesM
  247846. 21145N
  247847. 2/28/96W
  247848. 1990X
  247849. A    Sinou, D.B J. Chem. Res.  (Chem Highlights)CJprotecting group
  247850. allylation
  247851. allyl ether
  247852. palladium coupling
  247853. allyl carbonateI
  247854. HK$many further examples: 70-97% yieldsM
  247855. 21146N
  247856. 2/28/96W
  247857. 1990X
  247858. A Stafford, J. A.
  247859. Heathcock, C. H.B J. Org. Chem.  (Chem Highlights)C
  247860. secodaphniphyllineI
  247861. IK)total synthesis of (-)-secodaphniphyllineM
  247862. 21147N
  247863. 2/28/96W
  247864. 1990X
  247865. 5433Y
  247866. Durst, T.
  247867. Gabe, E. J.B J. Org. Chem.  (Chem Highlights)C
  247868. lactam alkylationI
  247869. 3 other examples, yields 80-90%M
  247870. 21148N
  247871. 2/28/96W
  247872. 1990X
  247873. 5525Y
  247874. !A*Zydowsky, T. M.
  247875. de Lara, E.
  247876. Spanton, S. G.B J. Org. Chem.  (Chem Highlights)C6lactone alkylation
  247877. allylation
  247878. hydrolysis
  247879. ester enolateI
  247880. KK:5 other examples, yields 66-82%, selectivities 5:1 to 31:1M
  247881. 21149N
  247882. 2/28/96W
  247883. 1990X
  247884. 5437Y
  247885. Boger, D. L.
  247886. Mathvink, R. J.B J. Org. Chem.  (Chem Highlights)CVfree radical cyclization
  247887. alkyl bromide
  247888. tributyltin hydride
  247889. ring enlargement
  247890. ozonolysisI
  247891. 2 other examples, yields 80-86%M
  247892. 21150N
  247893. 2/28/96W
  247894. 1990X
  247895. 5442Y
  247896. #A$Tucker, C. E.
  247897. Rao, S. A.
  247898. Knochel, P.B J. Org. Chem.  (Chem Highlights)CPdianion
  247899. grignard reagent
  247900. zinc reagent
  247901. conjugate addition
  247902. elimination of diester
  247903. MK213 other examples, yields 72-91%, Z/E 100:0 - 7:93M
  247904. 21151N
  247905. 2/28/96W
  247906. 1990X
  247907. 5446Y
  247908. Fukumoto, K.B J. Org. Chem.  (Chem Highlights)C9Cortisone
  247909. [4+2]-cycloaddition
  247910. o-quinondimethane
  247911. oxathianeI
  247912. NKAkey step in the first enantioselective synthesis of (+)-CortisoneM
  247913. 21152N
  247914. 2/28/96W
  247915. 1990X
  247916. 5626Y
  247917. Evans, D. A.
  247918. Fu, G. C.B J. Org. Chem.  (Chem Highlights)Cj1,4-reduction of enones
  247919. catecholborane
  247920. boron enolate
  247921. aldol reaction
  247922. acetate protection
  247923. selective reductionI
  247924. 10 examples 55-95% yieldM
  247925. 21153N
  247926. 2/28/96W
  247927. 1990X
  247928. 5678Y
  247929. Sengupta, S.
  247930. Snieckus, V.B J. Org. Chem.  (Chem Highlights)CXa-metallated enol carbamate
  247931. acyl anion equivalent
  247932. s-BuLi, TMEDA
  247933. alkylation
  247934. allyl halide
  247935. 14 examples, 40-85% yieldM
  247936. 21154N
  247937. 2/28/96W
  247938. 1990X
  247939. 5680Y
  247940. 'A$Sarkar, D. C.
  247941. Das, A. R.
  247942. Ranu, B. C.B J. Org. Chem.  (Chem Highlights)C.selective reduction
  247943. enone
  247944. ketone
  247945. Zn(BH4)2I
  247946. 21155N
  247947. 2/28/96W
  247948. 1990X
  247949. 5799Y
  247950. Mioskowski, C.
  247951. Falck, J. R.B J. Org. Chem.  (Chem Highlights)C
  247952. glycoside formation
  247953. ketal
  247954. pyranI
  247955. RKU23 examples, 25-88% yield, a:b ratio 65:35 - >95:5, no Ferrier rearrangement observedM
  247956. 21156N
  247957. 2/28/96W
  247958. 1990X
  247959. 5812Y
  247960. Yamamoto, H.
  247961. B J. Org. Chem.  (Chem Highlights)C"chiral ketal
  247962. enol ether
  247963. hemiacetalI
  247964. SKJ9 examples, 68-95% overall yield, towards total synthesis of (-)-LardolureM
  247965. 21157N
  247966. 2/28/96W
  247967. 1990X
  247968. 5814Y
  247969. *A)Collins, J. L.
  247970. Grieco, P. A.
  247971. Gross, R. S.B J. Org. Chem.  (Chem Highlights)C
  247972. )-Shinjulactone CI
  247973. 21158N
  247974. 2/28/96W
  247975. 1990X
  247976. 5816Y
  247977. Barrett, A. G. M.
  247978. Lebold, S. A.B J. Org. Chem.  (Chem Highlights)C=aldol condensation
  247979. vinyl lithium
  247980. ozonolysis
  247981. vinyl ether
  247982. azideI
  247983. UK%Towards the synthesis of Nikkomycin BM
  247984. 21159N
  247985. 2/28/96W
  247986. 1990X
  247987. 5818Y
  247988. Farina, V.B J. Org. Chem.  (Chem Highlights)CDpalladium catalyzed coupling
  247989. vinyl triflate
  247990. pyrrole
  247991. vinyl tin
  247992. cephenI
  247993. Pd2(dba)3 = tris(dibenzylideneacetonyl)bispalladium (0), NMP = N-methyl pyrrolidine, general method for the elaboration of cephen side chains, many examplesM
  247994. 21160N
  247995. 2/28/96W
  247996. 1990X
  247997. 5833Y
  247998. Moutet, J.-C.B J. Org. Chem.  (Chem Highlights)C1electrocatalytic reduction
  247999. a,b-unsaturated ketoneI
  248000. WK16 examples under various conditions, 9-100% yieldM
  248001. 21161N
  248002. 2/28/96W
  248003. 1990X
  248004. 5905Y
  248005. Caubere, P.B
  248006. J. Org. Chem. (Chem Highlights)C(ketone reduction
  248007. complex reducing agentsI
  248008. XK)12 examples under a variety of conditionsM
  248009. 21162N
  248010. 2/28/96W
  248011. 1990X
  248012. 5911Y
  248013. Caubere, P.
  248014. /B J. Org. Chem.  (Chem Highlights)C
  248015. alcohol epimerizationI
  248016. YK69 examples, 90-97% yield, 52:48 - 98:2 epimeric ratiosM
  248017. 21163N
  248018. 2/28/96W
  248019. 1990X
  248020. 5916Y
  248021. 0A(Dragisich, V.
  248022. Wulff, W. D.
  248023. Hoogsteen, K.B"Organometallics  (Chem Highlights)C1tungsten carbene complex
  248024. pyrroles
  248025. imine
  248026. acetyleneI
  248027. 10 examples 45-96% yieldsM
  248028. 21164N
  248029. 2/28/96W
  248030. 1990X
  248031. 2867Y
  248032. Hegedus, L.
  248033. derberg, B.B"Organometallics  (Chem Highlights)CCchromium carbene complex
  248034. tetrahydofurans
  248035. cyclopropane
  248036. cycloadditionI
  248037. 13 examples 5-92% yieldM
  248038. 21165N
  248039. 2/28/96W
  248040. 1990X
  248041. 3113Y
  248042. Ranu, B. C.
  248043. Chakraborty, R.B!Synth. Commun.  (Chem Highlights)C
  248044. epoxide opening
  248045. DowexI
  248046. 7 other examples 70-95% yieldM
  248047. 21166N
  248048. 2/28/96W
  248049. 1990X
  248050. 1751Y
  248051. von Itzstein, M.
  248052. Mocerino, M.B Synth. Commun. (Chem Highlights)C5benzyl ester
  248053. benzoic acid
  248054. diisopropylazodicarboxylateI
  248055. 21167N
  248056. 2/28/96W
  248057. 1990X
  248058. 2049Y
  248059. Kabalka, G. W.
  248060. Wang, Z.
  248061. 4B!Synth. Commun.  (Chem Highlights)C
  248062. hydroboration
  248063. amination
  248064. amineI
  248065. 9 other examples, 49-78% yieldM
  248066. 21168N
  248067. 2/28/96W
  248068. 1990X
  248069. 2113Y
  248070. Kende, A. S.
  248071. Thurston, J.B!Synth. Commun.  (Chem Highlights)C2nitro reduction
  248072. cyclization
  248073. cyclic N-hydroxylamideI
  248074. 7 other examples, 8-90% yieldM
  248075. 21169N
  248076. 2/28/96W
  248077. 1990X
  248078. 2133Y
  248079. 6A    Saigo, K.B!Synth. Commun.  (Chem Highlights)C?oxonium
  248080. acetal ester
  248081. enamine condenation
  248082. protected 1,3-diketoneI
  248083. 7 other examples, 43-85% yieldM
  248084. 21170N
  248085. 2/28/96W
  248086. 1990X
  248087. 2197Y
  248088. Demir, A. S.B!Synth. Commun.  (Chem Highlights)C&manganese triacetate oxidation
  248089. ketone
  248090. 15 other examples, 32-82% yieldM
  248091. 21171N
  248092. 2/28/96W
  248093. 1990X
  248094. 2279Y
  248095. Yamada, K.B!Synth. Commun.  (Chem Highlights)C
  248096. aldol condensationI
  248097. bKc3 other examples, 70-94% yield, syn/anti = 80:20 - 89:11.  Short synthesis of (
  248098. )-blastmycinolactolM
  248099. 21172N
  248100. 2/28/96W
  248101. 1990X
  248102. 2339Y
  248103. Adams, C. M.
  248104. Schemenaur, J. E.
  248105. 9B!Synth. Commun.  (Chem Highlights)C#selective reduction
  248106. aldehyde
  248107. ketoneI
  248108. 21173N
  248109. 2/28/96W
  248110. 1990X
  248111. 2359Y
  248112. :A Miginiac, L
  248113. Guyot, B.
  248114. Pornet, J.B!Synth. Commun.  (Chem Highlights)C7g-trimethylsilyl allyl boronic ester
  248115. imine
  248116. allyl silaneI
  248117. dK:synthesis of homoallylic amines.
  248118. 9 examples, 50-73% yield.M
  248119. 21174N
  248120. 2/28/96W
  248121. 1990X
  248122. 2409Y
  248123. Krapcho, A. P.
  248124. Kuell, C. S.B Synth. Commun. (Chem Highlights)C2protection of amines with BOC group.
  248125. BOC anhydrideI
  248126. 4 other examples 75-90% yieldM
  248127. 21175N
  248128. 2/28/96W
  248129. 1990X
  248130. 2559Y
  248131. <A1Olah, G. A.
  248132. Krishnamurti, R.
  248133. Surya Prakash, G. K.B
  248134. Synthesis  (Chem Highlights)C1g-trimethylsilyloxy nitrile
  248135. TMSCN
  248136. olefinic ketoneI
  248137. 21176N
  248138. 2/28/96W
  248139. 1990X
  248140. Katritzky, A.
  248141. Lam, J.
  248142. Yang, Z.B
  248143. Synthesis (Chem Highlights)C5acyl anion equivalent
  248144. benzyl bromide
  248145. Bt3CH
  248146. hydrolysisI
  248147. gK&9 othe examples, yields 58-98%; 73-92%M
  248148. 21177N
  248149. 2/28/96W
  248150. 1990X
  248151. Miltz, W.
  248152. Steglich, W.
  248153. Synthesis  (Chem Highlights)C!chiral enamine
  248154. imine
  248155. chloro amideI
  248156. hKQ2 more examples with chiral enamine, 60-91% yields, 92-98% ee, 4 related examplesM
  248157. 21178N
  248158. 2/28/96W
  248159. 1990X
  248160. Mikolajczyk, M.B
  248161. Synthesis  (Chem Highlights)C-sulfide oxidation
  248162. hydrogen peroxide
  248163. sulfoxideI
  248164. iK!12 other examples, 77-100% yieldsM
  248165. 21179N
  248166. 2/28/96W
  248167. 1990X
  248168. Ma, D.
  248169. Lu, X.B
  248170. Tetrahedron  (Chem Highlights)C.iridium catalyst
  248171. diene ester
  248172. acetylenic ester
  248173. 9 other examples, 0-92% yieldM
  248174. 21180N
  248175. 2/28/96W
  248176. 1990X
  248177. 6319Y
  248178. AA&Grigg, R.
  248179. Gunaratne, H. Q. N.
  248180. Kemp, J.B
  248181. Tetrahedron  (Chem Highlights)C$cycloaddition
  248182. imine
  248183. acetylenic esterI
  248184. 23 other examples, 16-83% yieldM
  248185. 21181N
  248186. 2/28/96W
  248187. 1990X
  248188. 6467Y
  248189. Kurozumi, S.B
  248190. Tetrahedron  (Chem Highlights)C8samarium iodide cyclization
  248191. alkylation
  248192. ortho ester
  248193. 21182N
  248194. 2/28/96W
  248195. 1990X
  248196. 6689Y
  248197. CA0Yadav, J. S.
  248198. Deshpande, P. K. 
  248199. Sharma, G. V. M. B
  248200. Tetrahedron  (Chem Highlights)
  248201. CC halo epoxide
  248202. acetylenic alcohol
  248203. 11 other examples, 72-88% yieldM
  248204. 21183N
  248205. 2/28/96W
  248206. 1990X
  248207. 7033Y
  248208. Tiecco, M.
  248209. Tingoli, M.B
  248210. Tetrahedron  (Chem Highlights)C$cyclization
  248211. lactone
  248212. olefinic nitrileI
  248213. 5 other examples, 62-67% yieldM
  248214. 21184N
  248215. 2/28/96W
  248216. 1990X
  248217. 7139Y
  248218. EA"Ballini, R.
  248219. Petrini, M.
  248220. Rosini, G.B
  248221. Tetrahedron  (Chem Highlights)C&a-nitro ketone
  248222. reduction
  248223. nitro alcoholI
  248224. 6 other examples, 50-85%M
  248225. 21185N
  248226. 2/28/96W
  248227. 1990X
  248228. 7531Y
  248229. Lipshutz, B. H.
  248230. Miller, T. A.B"Tetrahedron Lett (Chem Highlights)C4alcohol inversion
  248231. Mitsunobu inversion
  248232. chloro acetateI
  248233. pK%4 other examples with clean inversionM
  248234. 21186N
  248235. 2/28/96W
  248236. 1990X
  248237. 5253 Y
  248238. GA&Wachter-Jurcsak, N.
  248239. Scully, F. E., Jr.B
  248240. Tet Lett  (Chem Highlights)C
  248241. urethane alkylation
  248242. 3 other examples, 46-74% yieldM
  248243. 21187N
  248244. 2/28/96W
  248245. 1990X
  248246. 5261Y
  248247. Kraus, G. A.
  248248. Liras, S.B
  248249. Tet Lett  (Chem Highlights)C0cyclization
  248250. trichlorosilane
  248251. t-butylhydroperoxideI
  248252. 4 other examples, 60-84% yieldM
  248253. 21188N
  248254. 2/28/96W
  248255. 1990X
  248256. 5265Y
  248257. IA-Shambayati, S.
  248258. Crowe, W. E.
  248259. Schreiber*, S. L.B$Tetrahedron Lett.  (Chem Highlights)C
  248260. Pausand Khand cyclization
  248261. prep of cyclic a,b-unsaturated ketone
  248262. N-methylmorpholine N-oxide
  248263. protection of acetylene
  248264. cobalt hexacarbonyl I
  248265. sK79 other examples, 68-98% yield, selectivity = 4:1->25:1M
  248266. 21189N
  248267. 2/28/96W
  248268. 1990X
  248269. 5289Y
  248270. Taschner*, M. J.
  248271. Cyr, P. T.B$Tetrahedron Lett.  (Chem Highlights)CYDiels-Alder cyclization
  248272. prep of cyclohexadiene
  248273. diethylaluminum chloride
  248274. acetylenic ketoneI
  248275. tK75 other cyclization examples, 74-85% yield, 4:1 - 6.2:1M
  248276. 21190N
  248277. 2/28/96W
  248278. 1990X
  248279. 5297 Y
  248280. Gammill*, R. B.B$Tetrahedron Lett.  (Chem Highlights)CBreduction of a,b-unsaturated ketone
  248281. LiAlD4
  248282. prep of deutero alcoholI
  248283. 21191N
  248284. 2/28/96W
  248285. 1990X
  248286. 5301, 5303Y
  248287. Torii*, S.B$Tetrahedron Lett.  (Chem Highlights)
  248288. LCppalladium catalyzed coupling
  248289. vinyl iodide
  248290. palladium acetate
  248291. Pd(OAc)2
  248292. potassium cyanide
  248293. prep of b-cyanoalkeneI
  248294. 11 other examples, 14-81% yieldM
  248295. 21192N
  248296. 2/28/96W
  248297. 1990X
  248298. 5319Y
  248299. MA'Spears, G. W.
  248300. Nakanishi, K.
  248301. Ohfune*, Y.B$Tetrahedron Lett.  (Chem Highlights)C
  248302. palladium catalyzed lactonization
  248303. TBS protected urethane
  248304. tetrakis(triphenylphosphine)palladium
  248305. tetrabutylammonium fluoride
  248306. prep of cyclic urethaneI
  248307. wK66 other examples, 0-78% yield, syn/anti = 1.5:1 - 15:1M
  248308. 21193N
  248309. 2/28/96W
  248310. 1990X
  248311. 5339Y
  248312. Sakuraba*, H.
  248313. Ushiki, S.B$Tetrahedron Lett.  (Chem Highlights)C
  248314. chiral sulfoxide
  248315. prep of b-hydroxysulfoxide
  248316. prep of chiral alcohol
  248317. desulfurization
  248318. condensation
  248319. lithium diethyl amide
  248320. aryl ketone
  248321. Raney-nickelI
  248322. 8 other examples, 6-100% deM
  248323. 21194N
  248324. 2/28/96W
  248325. 1990X
  248326. 5349 Y
  248327. OA$Tokuda*, M.
  248328. Fujita, H.
  248329. Suginome*, H.B$Tetrahedron Lett.  (Chem Highlights)C2cyclization
  248330. prep of pyrrolidine
  248331. g-amino acetylene
  248332. 4 other examples, 80-98% yieldM
  248333. 21195N
  248334. 2/28/96W
  248335. 1990X
  248336. 5353Y
  248337. Bennett, R. B. III
  248338. Cha*, J. K.B$Tetrahedron Lett.  (Chem Highlights)Cssynthesis of (+)-Crotanecine
  248339. Wittig reaction
  248340. tosylation
  248341. azide displacement of tosylate
  248342. lactol
  248343. prep of cyclic imine
  248344. 21196N
  248345. 2/28/96W
  248346. 1990X
  248347. 5437Y
  248348. QA$Fujisawa*, T.
  248349. Takemura, I.
  248350. Ukaji, Y.B$Tetrahedron Lett.  (Chem Highlights)C/alkylation
  248351. ketone
  248352. methyl lithium
  248353. dimethyl zinc
  248354. 2 additional examplesM
  248355. 21197N
  248356. 2/28/96W
  248357. 1990X
  248358. 5479Y
  248359. RA    S.P TanisB
  248360. JACSCLMukaiyama Michael Aldol Reaction
  248361. Thioketene acetal
  248362. Trityl cation 
  248363. Lewis acidI
  248364. 21198N
  248365. 2/28/96V4Furans in Synthesis: Total Synthesis of Fastigilin CW
  248366. 1992X
  248367. 8349Y
  248368. Aoyama*, T.
  248369. Shioiri, T.B$Tetrahedron Lett.  (Chem Highlights)CEprotection of allylic alcohol
  248370. protecting group - methyl ether
  248371. TMSCHN2I
  248372. 11 other examples, 32-93% yieldM
  248373. 21199N
  248374. 2/28/96W
  248375. 1990X
  248376. 5507Y
  248377. Ley*, S. V.
  248378. TB$Tetrahedron Lett.  (Chem Highlights)C~Tetronasin
  248379. Sharpless epoxidation
  248380. cyclization
  248381. prep of tetrahydropyran
  248382. protection of diol
  248383. protecting group - dimethylacetonide
  248384. 21200N
  248385. 2/28/96W
  248386. 1990X
  248387. 5525Y
  248388. Soderquist*, J. A.
  248389. Santiago, B.B$Tetrahedron Lett.  (Chem Highlights)C<prep of alkene
  248390. vinyl bromide 
  248391. palladium catalyzed alkylationI
  248392. 6 other examples, 74-97% yieldM
  248393. 21201N
  248394. 2/28/96W
  248395. 1990X
  248396. 5541Y
  248397. VA+Barney, C. L.
  248398. Huber, E. W.
  248399. McCarthy*, J. R.B$Tetrahedron Lett.  (Chem Highlights)COprep of 2
  248400.  amine
  248401. imine reduction
  248402. titanium tetrachloride
  248403. sodium cyanoborohydrideI
  248404. 9 other examples, 52-82% yieldM
  248405. 21202N
  248406. 2/28/96W
  248407. 1990X
  248408. 5547Y
  248409. WA3Abdel-Magid*, A. F.
  248410. Maryanoff*, C. A.
  248411. Carson, K. G.B$Tetrahedron Lett.  (Chem Highlights)C@prep of 2
  248412.  amine
  248413. reduction of imine
  248414. sodium triacetoxyborohydrideI
  248415. 25 other examples, 80-91% yieldM
  248416. 21203N
  248417. 2/28/96W
  248418. 1990X
  248419. 5595Y
  248420. XA/Discordia, R. P.
  248421. Murphy, C. K.
  248422. Dittmer*, D. C.
  248423. XB$Tetrahedron Lett.  (Chem Highlights)CDprep of allylic alcohol
  248424. epoxy tosylate
  248425. tellurium
  248426. sodium borohydride
  248427. 8 other examples, 80-91% yieldM
  248428. 21204N
  248429. 2/28/96W
  248430. 1990X
  248431. 5603Y
  248432. Jefford*, C. W.B$Tetrahedron Lett.  (Chem Highlights)CRprep of a,b-unsaturated lactone
  248433. alkylation of silyl ketene acetal
  248434. silver triflate
  248435. 21205N
  248436. 2/28/96W
  248437. 1990X
  248438. 5741Y
  248439. ZA0Choudary*, B. M.
  248440. Durgaprasad, A.
  248441. Valli, V. L. K.B$Tetrahedron Lett.  (Chem Highlights)CRprep of keto alcohol
  248442. selective oxidation
  248443. chromia pillared montmorillonite catalystI
  248444. KtCr-PILC: Chromia pillared montmorillonite catalyst
  248445. 10 examples, four with selective oxidation of 2
  248446.  over 1
  248447.  alcoholsM
  248448. 21206N
  248449. 2/28/96W
  248450. 1990X
  248451. 5785Y
  248452. Vidari*, G.
  248453. Garlaschelli, L.B$Tetrahedron Lett.  (Chem Highlights)CTprotection of ketone, aldehyde
  248454. protecting group - thio ketal
  248455. ethanethiol
  248456. lanthanide
  248457. K'7 aldehydes (55-90%), 6 ketones (0-93%)M
  248458. 21207N
  248459. 2/28/96W
  248460. 1990X
  248461. 5815Y
  248462. Lautens*, M.
  248463. \B$Tetrahedron Lett.  (Chem Highlights)CqClaisen rearrangement
  248464. vinyl silane
  248465. vinyl stannane
  248466. Tin Chemistry
  248467. allylic alcohol
  248468. prep of allylic stannane, silane
  248469. 9 other examples, 53-86%M
  248470. 21208N
  248471. 2/28/96W
  248472. 1990X
  248473. 5829Y
  248474. Paley*, R. S.
  248475. Snow, S. R.B$Tetrahedron Lett.  (Chem Highlights)C8palladium catalzed coupling
  248476. alane
  248477. prep of sulfoxyl dieneI
  248478. 9 examples, 35-87%M
  248479. 21209N
  248480. 2/28/96W
  248481. 1990X
  248482. 5853Y
  248483. Williams*, D. R.
  248484. Benbow, J. W.B$Tetrahedron Lett.  (Chem Highlights)C
  248485. imine alkylation
  248486. allyl bromide
  248487. 8 examples, 51-77%M
  248488. 21210N
  248489. 2/28/96W
  248490. 1990X
  248491. 5881Y
  248492. Shea*, K. J.B$Tetrahedron Lett.  (Chem Highlights)ChDiels-Alder reaction
  248493. deprotection of ester, alcohol
  248494. protecting group - diphenyl silyl
  248495. potassium fluorideI
  248496. 21211N
  248497. 2/28/96W
  248498. 1990X
  248499. 5885Y
  248500. Huang*, Y-Z.
  248501. Liao, Y.B$Tetrahedron Lett.  (Chem Highlights)CLolefination of ketone
  248502. diazo ester
  248503. tributyl antimonate
  248504. prep of diester olefinI
  248505. 18 examples, 62-98%M
  248506. 21212
  248507. 2/28/96W
  248508. 1990X
  248509. 5897Y
  248510. Sugimura*, H.B$Tetrahedron Lett.  (Chem Highlights)C
  248511. allyl silane
  248512. a-alkoxy aldehydeI
  248513. 21213N
  248514. 2/28/96W
  248515. 1990X
  248516. 5909Y
  248517. bA)Harmata*, M.
  248518. Gamlath, C. B.
  248519. Barnes, C. L.B$Tetrahedron Lett.  (Chem Highlights)CGcycloaddition
  248520. Lewis acid
  248521. titanium tetrachloride
  248522. enol ether
  248523. bromination
  248524. 21214N
  248525. 2/28/96W
  248526. 1990X
  248527. 5981Y
  248528. Lange*, G. L.
  248529. Gottardo, C.B$Tetrahedron Lett.  (Chem Highlights)CNfree radical fragmetation
  248530. tributyl tin hydride
  248531. iodide
  248532. prep of exocylic olefin
  248533. 4  other examples 51-90%M
  248534. 21215N
  248535. 2/28/96W
  248536. 1990X
  248537. 5985Y
  248538. dA Koreeda*, M.
  248539. Teng, K.
  248540. Murata, T.B$Tetrahedron Lett.  (Chem Highlights)Ccsynthesis of shikimi acic
  248541. Diels-Alder reaction
  248542. hydroquinone monomethyl ether
  248543. a,b-unsaturated ester
  248544. 21216N
  248545. 2/28/96W
  248546. 1990X
  248547. 5997Y
  248548. eA!Asami*, Masatoshi
  248549. Inoue, Seiichi
  248550. Chemistry LettersC<prep of chiral alcohol
  248551. diethylzinc addition
  248552. chiral catalyst
  248553. eKeselectivity of reaction decreases with increased reaction temperatre or with the use of less catalystM
  248554. 21217N
  248555. 2/28/96VXEnantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Chiral Hydroxy AminalW
  248556. 1991X
  248557. 685-688
  248558. fAGYamada*, Tohru
  248559. Takahashi, K.
  248560. Kato, K.
  248561. Takai, T.
  248562. Inoki, S.
  248563. Mukaiyama, T.B
  248564. Chemistry LettersCVBaeyer-Villiger oxidation
  248565. bis(dipivaloylmethanato)nickel(II)
  248566. Ni(dpm)2
  248567. prep of lactone
  248568. 21218N
  248569. 2/28/96V
  248570. The Baeyer-Villiger Oxidation of Ketones Catalyzed by Nickel(II) Complexes with Combined Use of Molecular Oxygen and an AldehydeW
  248571. 1991X
  248572. 641-644
  248573. gA4Horiuchi*, C. Akira
  248574. Nishio, Y.
  248575. Gong, D.
  248576. Fujisaki, T.B
  248577. Chemistry LettersC2prep of a-alkoxyl and a-nitroso iodides
  248578. iodineI
  248579. KWR can also be ethyl, n-propyl, i-propyl, and CH2CH2OH using the corresponding alcohols M
  248580. 21219N
  248581. 2/28/96V`A New Alkoxyiodination and Nitratoiodination of Olefins Using Iodine-Cerium(IV) Ammonium NitrateW
  248582. 1991X
  248583. 607-610
  248584. hA4Kobayash, Shu
  248585. Tsuchiya, Yoshikazu
  248586. Mukaiyama, TeruakiB
  248587. Chemistry LettersC>Lewis acid
  248588. silyl cyanation
  248589. prep of a-trimethylsilyloxy cyanideI
  248590. 21220N
  248591. 2/28/96VnEnantioselective Addition Reaction of Trimethylsilyl Cyanide with Aldehydes Using a Chiral Tin(II() Lewis AcidW
  248592. 1991X
  248593. 541-544
  248594. iA-Kobayashi, S.
  248595. Tsuchiya, Y.
  248596. Mukaiyama, TeruakiB
  248597. Chemistry LettersC
  248598. silyl cyanation
  248599. TMSCNI
  248600. yields up to 98%, most amines work well including TEA, diisopropylethylamine, TMEDA, DIPA, tetramethylpiperdine.  R = straight chain aldehydes, aromatic aldehydes, pivalaldehyde, furfural.  Other catalysts such as Bu3P, Ph3As and Ph3Sb work as well.M
  248601. 21221N
  248602. 2/28/96V
  248603. A Facile Synthesis of Cyanohydrin Trimethylsilyl Ethers by the Addition Reaction of Trimethylsilyl Cyanide with Aldehydes under Basic ConditionsW
  248604. 1991X
  248605. 537-540
  248606. jA4Mukaiyama, T.
  248607. Takashima, T.
  248608. Katsurada, M.
  248609. Aizawa, H.B
  248610. Chemistry LettersC9prep of a-glucosides
  248611. tin tetrachloride
  248612. silver perchlorateI
  248613. 21222N
  248614. 2/28/96
  248615. A Highly Stereoselective Synthesis of a-Glucosides from 1-O-Acetyl Glucose by Use of Tin(IV) Chloride - Silver Perchlorate Catalyst SystemW
  248616. 1991X
  248617. 533-536
  248618. Narasaka, K.
  248619. Okauchi, T.B
  248620. Chemistry LettersCpoxidation
  248621. allyl sulfide
  248622. silyl enol ether
  248623. [2,3]-sigmatropic rearrangement
  248624. a-phenylthio-g,d-unsaturated ketoneI
  248625. CAN oxidizes the allylic sulfide to the organsulfur cation radical which then reacts with the silyl enol ether.  The radical intermediate is then oxidized by the second equivalent of CAN to form the b-keto sulfonium salt.  The sulfonium salt is then deprotonated with the second equivalent of silyl enol ether to form the sulfonium ylide followed by rearangement to form the a-phenylthio g,d-unsaturated ketone
  248626. 21223N
  248627. 2/28/96V
  248628. Generation of Cation Radicals from Allylic Sulfides and Their Reactions with Silyl Enol Ethers by the Use of Cerium(IV) Ammonium NitrateW
  248629. 1991X
  248630. 515-518
  248631. lA-Yoda*, Hidemi
  248632. Shirakawa, K.
  248633. Takabe*, Kunihiko
  248634. Chemistry LettersCyGrignard reaction
  248635. sodium borohydride reduction
  248636. chiral imide
  248637. hydroxy amide
  248638. lactone formation
  248639. silyl ether
  248640. chiral butenolideI
  248641. 21224N
  248642. 2/28/96V
  248643. Novel Asymmetric Synthesis of g-Alkylated Lactones via Successive Alkylation and Reduction of Chiral Cyclic Imides with C2-SymmetryW
  248644. 1991X
  248645. 489-490
  248646. Suda, S.
  248647. Mukaiyama, T.B
  248648. Chemistry LettersC3glycosylation
  248649. triflic anhydride
  248650. oxotitanium speciesI
  248651. yields are better in CH2Cl2, but a better stereoselectivity was attained in Et2O. Other alcohols or silyl ethers are also utilized.M
  248652. 21225N
  248653. 2/28/96V
  248654. Stereoselective Synthesis of 1,2-trans-Ribofuranosides from 1-Hydroxy Sugars by the use of [1,2-Benzenediolato(2-)-O,O']oxotitanium and Trifluorometanesulfonic AnhydrideW
  248655. 1991X
  248656. 431-434
  248657. nAHSasaki, K.
  248658. Mori, T.
  248659. Doi, Y.
  248660. Kawachi, A.
  248661. Aso, Y.
  248662. Otsubo, T.
  248663. Ogura*, FumioB
  248664. Chemistry LettersCZi-Bu2AlTePh
  248665. tellurium nucleophile
  248666. acetal
  248667. tosylate
  248668. mesylate
  248669. epoxide opening
  248670. organotelluriumI
  248671. 21226N
  248672. 2/28/96
  248673. nVlNucleophilic Reactions of Acetals, Alkyl Sulfonates, and Oxiranes with Diisobutylaluminum BenzenetellurolateW
  248674. 1991X
  248675. 415-418
  248676. oA&Hirano, M.
  248677. Oose, M.
  248678. Morimoto*, TakashiB
  248679. Chemistry LettersC'prep of lactone
  248680. ketone
  248681. oxone
  248682. oxidation
  248683. 7 other examples 23-85% yieldM
  248684. 21227N
  248685. 2/28/96V
  248686. A Novel Synthesis of Lactones by the Oxidation of Alicyclic Ketones with Oxone in Aprotic Solvent in the Presence of "Wet-Alumina"W
  248687. 1991X
  248688. 331-332
  248689. pA0Shibata*, Ikuya
  248690. Yoshida, T.
  248691. Baba, A.
  248692. Matsuda, H.B
  248693. Chemistry LettersCoprep of alcohol
  248694. reduction
  248695. Bu3SnH
  248696. tributyl tin hydride
  248697. tetrabutyl ammonium fluoride
  248698. tetrabutyl ammonium chlorideI
  248699. reduction also works with tetrabutyl ammonium chloride at higher temperatures.  Reduction does not remove aryl halides.  Resulting tin alkoxide can be used for O-alkylation with BnBr, cinnamyl bromide and BzCl.M
  248700. 21228N
  248701. 2/28/96V:Characteristic Reduction of Ketones by Bu3SnH-Bu4NX SystemW
  248702. 1991X
  248703. 307-310
  248704. qA2Takai, T.
  248705. Yamada, T.
  248706. Rhode, O.
  248707. Mukaiyama*, TeruakiB
  248708. Chemistry LettersC
  248709. oxidation
  248710. prep of a-hydroxy ketone and a-hydroxy ester
  248711. Ni(mac)2
  248712. deprotection of silyl ether
  248713. bis(3-methyl-2,4-pentanedionato)nickel(II)I
  248714. sOxygenation works with silyl ketene acetals, and TBS silyl enol ethers as well (with higher yield than TMS enol ether).  Silyl rearrangement via siloxy epoxides is postulated. RCHO = isobutyraldehyde.  The aldehyde accepts one oxygen to form the corresponding carboxylic acid which would cause the decompostion of silyl ketene acetals to yield the carboxylic acid ester. 
  248715. 21229N
  248716. 2/28/96V
  248717. Oxygenation of Silyl Enol Ethers and Silyl Ketene Acetals with Molecular Oxygen and Aldehyde Catalyzed by Nickel(II) Complex.  A Convenient Method for the Preparation of a-Hydroxy Carbonyl CompoundsW
  248718. 1991X
  248719. 281-284
  248720. rA%Kitagawa, O.
  248721. Sato, T.
  248722. Taguchi*, TakeoB
  248723. Chemistry Letters
  248724. iodolactonization
  248725. haloetherification
  248726. Ti(Oi-Pr)4
  248727. halocyclization
  248728. prep of iodo lactone
  248729. homoallyic chiral induction
  248730. Lewis acidI
  248731. Bidentate bonding of Ti(IV) with olefinic acid plays an important role to achieve an increased cis-selectivity in the halolactonization.  When X = CH2OH selectivity is reversed favoring the trans isomer.M
  248732. 21230N
  248733. 2/28/96VpEffect of Ti(Oi-Pr)4 on Stereoselectivity of Halocyclization of 2-Substituted 4-Pentenoic Acid and 4-Penten-1-olW
  248734. 1991X
  248735. 177-180
  248736. sA/Ukaji, Y.
  248737. Kume, K.
  248738. Watai, T.
  248739. Fujisawa*, TamotsuB
  248740. Chemistry LettersCGallyl metal
  248741. allyl Grignard
  248742. CeCl3
  248743. alkoxymethyl oxime ether
  248744. allyl lithiumI
  248745. (E)-oxime ether shows better face selectivity than (Z)-oxime ether.  Cis compound is preferred 86:12 when M = MgBr-CeCl3 with (E) oxime, 87% yield.  Trans is preferred 3:97 with allyl lithium using (E)-oxime, 99% yield.  It is presumed that the simultaneous coordination to metal by the three heteroatoms, was crucial for either diastereoface discrimination, because in the (Z) oxime ether (which shows poor selectivity) this simultaneous coordination is impossible.  
  248746. 21231N
  248747. 2/28/96VnDiastereofacial Discrimination in the Reaction of Chiral Alkoxymethyl Oxime Ethers with Alyl Metallic ReagentsW
  248748. 1991X
  248749. 173-176
  248750. tA%Tomooka, K.
  248751. Wei, S-Y.
  248752. Nakai*, TakeshiB
  248753. Chemistry LettersCranionic oxy-Cope rearrangement
  248754. 18-Cr-6
  248755. [2,3]-Wittig rearrangement
  248756. hydrogenation
  248757. [3,3]-sigmatropic rearrangementI
  248758. E selectivity decreases in the order: Z/trans > E/trans > E/cis >> Z/cis. Paper shows transition-state model to explain stereochemistry observed, where relative stability of the T.S. is determined primarily by the following two factors; 1. the conformation with the larger total number of pseudo-axial substituents is less favorable and 2. the presence of a pseudo-1,3-diaxial interaction between the oxy (OK) and methyl groups makes the conformation much less favorable.
  248759. 21232N
  248760. 2/28/96V_Acyclic Oxy-Cope Rearrangement.  Dependence of E/Z Stereoselection on Substrate StereochemistryW
  248761. 1991X
  248762. 43-46
  248763. uA2Yamada, T.
  248764. Rhode, O.
  248765. Takai, T.
  248766. Mukaiyama*, TeruakiB
  248767. Chemistry LettersCqprep of carboxylic acid
  248768. oxidation
  248769. aldehyde
  248770. Ni(dmp)2
  248771. bis[1,3-di(p-methoxyphenyl)-1,3-propanedionato]nickel(II)
  248772. Nickel complexes having 1,3 diketone-type ligands work the best. Alcohol, ether or aromatic hydrocarbon solvents give poor yields of acids, but ketones or ester solvents are appropriate.  Yields from 63-91% depending on steric bulk surrounding the aldehyde
  248773. 21233N
  248774. 2/28/96VdOxidation of Aldehydes into Carboxylic Acids with Molecular Oxygen Using Nickel(II) Complex CatalystW
  248775. 1991X
  248776. vA2Yamada, T.
  248777. Takai, T.
  248778. Rhode, O.
  248779. Mukiayama*, TeruakiB
  248780. Chemistry LettersCcprep of epoxide
  248781. olefin
  248782. Ni(dmp)2
  248783. oxidation
  248784. bis[1,3-di(p-methoxyphenyl)-1,3-propanedionata]nickel(II)I
  248785. Aldehydes with a secondary or tertiary carbon next to the carbonyl work best.  1,3 diketones are best as ligands for Ni complex.  Examples of oxidation of di- and tri-substituted olefinsM
  248786. 21234N
  248787. 2/28/96VyHighly Efficient Method for Epoxidation of Olefins with Molecular Oxygen and Aldehydes Catalyzed by Nickel(II) Complexes.W
  248788. 1991X
  248789. Kamimura*, Akio
  248790. Yamamoto, A.B
  248791. Chemistry Letters
  248792. wCaene reaction
  248793. D2-isoxazoline
  248794. prep of hyroxy alkene
  248795. Lewis acid
  248796. chelation and non-chelation control I
  248797. Using SnCl4, 70% yield 99.5:.05 syn/anti (-78
  248798. C), TiCl2(OiPr)2, 74% 95:5 syn/anti (RT), Et2AlCl, 59% 0:100 syn/anti (-78
  248799. C).Stereoselectivity of Sn and Ti Lewis acids is due to coordination of metal to formyl O and N of isoxazoline ring to form a bicyclic complex.  The olefin then attacks from the opposite side of other ring structure to give syn products.  Et2AlCl proceeds via non-chelation control to give predominantly anti products. 
  248800. 21235N
  248801. 2/28/96V<Diastereoselective Ene Reaction of 3-Formyl-D2-isoxazolines.W
  248802. 1990X    1991-1994
  248803. L. S. LiebeskindB
  248804. JACSC=Grignard Reagent
  248805. Molybdenum Complex
  248806. Reduction
  248807. TetrahydropyranI
  248808. K3Synthesis of the cis-tetrahydropyran is also given M
  248809. 21236N
  248810. 2/28/96
  248811. Enantiospecific Synthesis by Transformations of Chiral Pool-Derived Metal p-Complexes.  A Strategy for the Introduction of Substituents on a Pyranose-Derived Lateral p-Ligand either Syn or Anti to the Coordinating MetalW
  248812. 1993X
  248813. yA&Mukaiyama, T.
  248814. Shiina, I.
  248815. Kobayashi, S.B
  248816. Chemistry LettersClAldol reaction
  248817. dihydroxylation reaction
  248818. a,b-unsaturated aldehyde
  248819. silyl enol ether
  248820. a-benzyloxy thioesterI
  248821. 21237N
  248822. 2/28/96V
  248823. A Convenient and Versatile Route for the Stereoselective Synthesis of Monosaccharides via Key Chiral Synthons Prepared from Aciral Sources.W
  248824. 1990X    2201-2204
  248825. S. InokiB
  248826. Chem. Lett.C%epoxidation
  248827. oxygen
  248828. Vanadium catalyzedI
  248829. 21238N
  248830. 2/28/96W
  248831. 1991X
  248832. T. MukaiyamaB
  248833. Chem. Lett.C4Aldol reaction
  248834. Silyl enol ether
  248835. Indium trichloride 
  248836. 21239N
  248837. 2/28/96W
  248838. 1991X
  248839. A. I. MeyersB
  248840. JACSCGMetalation
  248841. a-aminocopper carbanion
  248842. carbamate
  248843.  a-aminolithium carbanion I
  248844. 21240N
  248845. 2/28/96
  248846. a-Alkylation of and Stereochemistry of cis- and trans -Decahydroquinolines Mediated by the Formamidine and Boc Activating Groups.  Synthesis of Pumiliotoxin.W
  248847. 1993X
  248848. 6652Y
  248849. J. M. NussB
  248850. JACSC(annulation 
  248851. alkyne mediated cyclization
  248852. 21241N
  248853. 2/28/96V
  248854. Transition -Metal  Catalyzed Strategies for the Synthesis of Neocarzinostatin Chromophor and Analogues: Intramolecular Delivery of Palladium Controls Construction of the Biologically Relevent Dienediyne Core W
  248855. 1993X
  248856. 6991Y
  248857. A. H. HoveydaB
  248858. JACSC
  248859. homoallylic alcohols
  248860. alkene I
  248861. 21242N
  248862. 2/28/96V0Zirconium- Catalyzed Asymmetric CarbomagnesationW
  248863. 1993X
  248864. 6997Y
  248865. E. Tagliavini
  248866. A. Umani-RonchiB
  248867. JACSC=Allylstannane
  248868. Organotin Chemistry
  248869. Titanium Binapthol CatalystI
  248870. 21243N
  248871. 2/28/96V6Catalytic Asymmetric Synthesis of Homoallylic AlcoholsW
  248872. 1993X
  248873. 7001Y
  248874. S. J. DanishefskyB
  248875. JACSC/Benzyne
  248876. Diazonium salt
  248877. cycloaddition
  248878. thioacetalI
  248879. 21244N
  248880. 2/28/96
  248881. VpTotal Synthesis of the Novel Benzopentathiepin Varacinium Trifluoroacetate: The Viability of "Varacin Free Base"W
  248882. 1993X
  248883. 7017Y
  248884. S. J. DanishefskyB
  248885. JACSC)Pentathiepin
  248886. Formylation
  248887. Sulfur ChemistryI
  248888. 21245N
  248889. 2/28/96VpTotal Synthesis of the Novel Benzopentathiepin Varacinium Trifluoroacetate: The Viability of "Varacin Free Base"W
  248890. 1993X
  248891. 7016Y
  248892. A. G. MeyersB
  248893. JACSC!palladium coupling
  248894. OrganostannaneI
  248895. 21246N
  248896. 2/28/96VwA Reaction Cascade Leading to 1,6-Didehydro[10]annulene- 1,5-Dehydronaphthalene Cyclizaton Initiated by Thiol Addition W
  248897. 1993X
  248898. 7021Y
  248899. A. G. MeyersB
  248900. JACSC
  248901. biradical
  248902. cycloaromatizationI
  248903. 21247N
  248904. 2/28/96VwA Reaction Cascade Leading to 1,6-Didehydro[10]annulene- 1,5-Dehydronaphthalene Cyclizaton Initiated by Thiol Addition W
  248905. 1993X
  248906. 7021Y
  248907. R. L. FunkB
  248908. JACSC9alkynes
  248909. annulation
  248910. carbanion
  248911. cyclization
  248912. Wittig Reaction
  248913. 21248N
  248914. 2/28/96
  248915. Facile Intramolecular Carbolithiation Reactions of Alkylthio- and Alkoxyacetylenes by Stabilized Carbanions.  A Novel Strategy for the Synthesis of Functionalized Carbocycles W
  248916. 1993X
  248917. 7023Y
  248918. R. L. FunkB
  248919. JOCC.Ireland Claisen Rearrangement
  248920. Silyl Enol EtherI
  248921. 21249N
  248922. 2/28/96VAStereoselective Construction of the Complete Ingenane Ring SystemW
  248923. 1993X
  248924. 5873Y
  248925. 58 (22)
  248926. J. A. MarshallB
  248927. JOCCROrganotin
  248928. Lewis Acid Catalyzed Allyl Tin Addition
  248929. Osmium Tetroxide DihydroxylationI
  248930. 21250N
  248931. 2/28/96V
  248932. Stereoselective Synthesis of Long Chain Polyols by Sequential Homologation of Enals with Nonracemic g-Siloxy Allylic Stannanes and Directed HydroxylationW
  248933. 5876Y
  248934. 58 (22)
  248935. P. KnochelB
  248936. JACSC:Zinc 
  248937. Organozinc
  248938. annulation 
  248939. cyclization
  248940. cuprate
  248941. PalladiumI
  248942. 21251N
  248943. 2/28/96VyPalladium- Catalyzed Iodine- Zinc Exchange Reactions.  A New Palladium- Mediated Intramolecular Carbozincation of AlkenesW
  248944. 1993X
  248945. 7027Y
  248946. A    H. TakayaB
  248947. JACSC<Hydroformylation
  248948. Rhodium catalyst
  248949. aldehyde synthesis
  248950. alkene
  248951. 21252N
  248952. 2/28/96ViHighly Enantioselective Hydroformylation of Olefins Catalyzed by New Phosphinephosphite - Rh(1) ComplexesW
  248953. 1993X
  248954. 7033Y
  248955. A    K. MikamiB
  248956. JACS C'Lewis Acid
  248957. Titanium Binaphthol CatalystI
  248958. 21253N
  248959. 2/28/96V
  248960. Enantioselective and Diastereoselective Catalysis of the Mukaiyama Aldol Reaction: Ene Mechanism in Titanium- Catalyzed Aldol Reactions of Silyl Enol Ethers W
  248961. 1993X
  248962. 7039Y
  248963. K. B. SharplessB
  248964. JACSC=Dihydroxylation
  248965. Alkene
  248966. Kinetics and Reaction Rates
  248967. DABCOI
  248968. 21254N
  248969. 2/28/96VcA Dramatic Ligand Effect on the Relative Reactivities of Substituted Alkenes with Osmium Tetroxide W
  248970. 1993X
  248971. 7047Y
  248972. M. J. BurkB
  248973. JACSCUAsymmetric Hydrogenation Reaction
  248974. Cationic Rhodium Complex
  248975. Chiral Phosphorous LigandsI
  248976. 21255N
  248977. 2/28/96
  248978. Preparation and Use C-2 -Symmetric Bis (phospholanes): Production of a-Amino Acids Derivatives via Highly Enantioselective Hydrogenation Reactions.  W
  248979. 1993X
  248980. 10125Y
  248981. Y. YamamotoB
  248982. JACSC0Conjugate Addition
  248983. Cuprate
  248984. Diels-Alder Reaction
  248985. 21256N
  248986. 2/28/96V}Conformationally Rigid Acyclic 23,2,6,6-Tetramethyl-3,5-Heptanediol (TMHDiol) Derivative as a New Class of Chiral AuxiliariesW
  248987. 1993X
  248988. 10139Y
  248989. W. H. Pearson B
  248990. JACSC"Azide
  248991. Amine
  248992. Annulation
  248993. CyclizationI
  248994. 21257N
  248995. 2/28/96V
  248996. Intramolecular Schmidt Reactions of Azides with Carbocations: Synthesis of Bridged Bicyclic and
  248997. Fused-Bicyclic Tertiary Amines  W
  248998. 1993X
  248999. 10183Y
  249000. H. YamamotoB
  249001. JACSC>Homoallylic Alcohol
  249002. Aldehyde
  249003. Ketone
  249004. Organotin Reagent
  249005. StannaneI
  249006. 21258N
  249007. 2/28/96VaHighly Chemoselective Allylation of Carbonyl Compounds with Tetraallyltin in Acidic Aqueous MediaW
  249008. 1993X
  249009. 10356Y
  249010. M. ShibasakiB
  249011. CILanthanides
  249012. Enantioselective Aldol Reaction
  249013. Chiral Alcohol
  249014. Henry ReactionI
  249015. K.Structure of catalyst determined by NMR and MSM
  249016. 21259N
  249017. 2/28/96V
  249018. Catalytic Asymmetric Nitroaldol Reaction Using Optically Active Rare Earth BINOL Complexes: Investigation of the Catalyst StructureW
  249019. 1993X
  249020. 10372Y
  249021. A. J. PearsonB
  249022. JACSI
  249023. 21260N
  249024. 2/28/96VeChiral Auxiliary- Directed Asymmetric Nucleophile Additions to Arene- Manganese Tricarbonyl ComplexesW
  249025. 1993X
  249026. 10379Y
  249027. S. DenmarkB
  249028. JACSCgAcylation
  249029. Alkylation
  249030. Hydride Reduction
  249031. Elimination
  249032. Olefin Synthesis
  249033. Horner Emmons Wadsworth Reaction
  249034. 21261N
  249035. 2/28/96VVA New, General, and Stereoselective Method for the Synthesis of Trisubstituted AlkenesW
  249036. 1993X
  249037. 10386Y
  249038. A. B. Holmes
  249039. JACSCZClaisen Rearrangement
  249040. Eight Membered Lactone Synthesis
  249041. Diene
  249042. Selenium Chemistry 
  249043. OxidationI
  249044. 21262N
  249045. 2/28/96V
  249046. Synthesis of (+)-LaurencinW
  249047. 1993X
  249048. 10400Y
  249049. A. B. HolmesB
  249050. C1Hydrosilation
  249051. Platinum Catalyst
  249052. Alcohol SynthesisI
  249053. 21263N
  249054. 2/28/96V
  249055. Synthesis of (+)-LaurencinW
  249056. 1993X
  249057. 10400Y
  249058. S. L. SchreiberB
  249059. JACSC4Friedel- Crafts
  249060. Lewis Acid
  249061. Silver Triflate
  249062. PhthalideI
  249063. 21264N
  249064. 2/28/96VCTotal Synthesis of Di- and Tri- O- methyl Dynamycin A Methyl EstersW
  249065. 1993X
  249066. 10378Y
  249067. B. M. TrostB
  249068. JACSC
  249069. Alkene
  249070. 21265N
  249071. 2/28/96VnRuthenium- Catalyzed Addition of Allyl Alcohols and Acetylenes.  A Simple Synthesis of g,d-Unsaturated KetonesW
  249072. 1993X
  249073. 10402Y
  249074. H. Yamamoto B
  249075. JACSC0Aldol Reaction
  249076. Lewis Acid
  249077. Boron-Ligand Catalyst
  249078. 21266N
  249079. 2/28/96VHMechanistic Studies of a CAB- Catalyzed Asymmetric Diels-Alder Reaction W
  249080. 1993X
  249081. 10412Y
  249082. S. F. Martin
  249083. JACSC1Enamine
  249084. Siloxyfuran
  249085. Amino-Aldol Reaction
  249086. AldehydeI
  249087. 21267N
  249088. 2/28/96V^Novel Applications of Vinylogous Mannich Reactions.  Total Synthesis of Rugulovasines A and B W
  249089. 1993X
  249090. 10450Y
  249091. S. F. Martin
  249092. CCCyclization
  249093. SRN1 Reaction
  249094. Annulation
  249095. Aryl Bromide
  249096. Lactone SynthesisI
  249097. 21268N
  249098. 2/28/96V^Novel Applications of Vinylogous Mannich Reactions.  Total Synthesis of Rugulovasines A and B W
  249099. 1993X
  249100. 10450Y
  249101. T. ToruB
  249102. JACSC=Sulfoxide
  249103. Boron Chemistry
  249104. Radical Chemistry
  249105. Chelation ControlI
  249106. 21269N
  249107. 2/28/96VWHighly B- Stereoselectivity in Asymmetric Radical Addition to a-SulfinylcyclopentenonesW
  249108. 1993X
  249109. 10464Y
  249110. H. YamatakaI
  249111. 21270N
  249112. 2/28/96V
  249113. Distiniction between  Polar and Electron- Transfer Routes.  A Mechanistic Study on the Wittig Reactions of Nonstabilized Ylides W
  249114. 1993X
  249115. 8570Y
  249116. B. Giese
  249117. D. CurranB
  249118. JACSC=Iodine Transfer Reaction
  249119. Diastereoselective Radical Reaction
  249120. The level of diastereoselectivity depends on the size of the alkyl substituent on the radical.  Tertiary radicals give high syn selectivity, secondary groups lead to moderate syn selectivity, and primary groups show completely unselective reactions.  A new steric model has been proposed on the basis of AM1 calculations.  This transition state model postulates attack of the reagent on the radical between the medium and large groups and anti to the small group. 
  249121. 21271N
  249122. 2/28/96V
  249123. 1,2-Asymmetric Induction in Reactions of Nonconjugated Acyclic Radicals:  A New Model for Highly Selective Atom-Transfer Reactions of Alkyl-Substituted Radicals W
  249124. 1993X
  249125. 8585Y
  249126. H. J. ReichB
  249127. JACSI
  249128. 21272N
  249129. 2/28/96V
  249130. A Nuclear Magnetic Resonance Spectroscopic Technique for the Characterization of Lithium Ion Pair Structures in THF and THF/HMPA SolutionW
  249131. 1993X
  249132. 8728Y
  249133. M. F. Ruiz-LopezB
  249134. JACSC
  249135. Computational ChemistryI
  249136. 21273N
  249137. 2/28/96
  249138. VVSolvent Effects on the Mechanism and Selectivities of Asymmetric Diels-Alder ReactionsW
  249139. 1993X
  249140. 8780Y
  249141. B. M. TrostB
  249142. JACSCHRuthenium Complex
  249143. Annulation
  249144. Alkyne
  249145. Cyclization
  249146. Transition Metal ComplexI
  249147. 21274N
  249148. 2/28/96VV1,5-Cyclooctadiene as a Bis-Homodiene Partner in a Metal-Catalyzed [4+2] CycloadditionW
  249149. 1993X
  249150. 8831Y
  249151. T. TaguchiB
  249152. JACSCDHomoallylic Alcohols
  249153. Allyl ethers
  249154. Allylzirconium Reagent
  249155. Annulation
  249156. 21275N
  249157. 2/28/96V
  249158. Zirconium-Mediated, Highly Diastereoselective Ring Contraction of Carbohydrate Derivatives:  Synthesis of Highly Functionalized, Enantiomerically Pure CarbocyclesW
  249159. 1993X
  249160. 8835Y
  249161. K. C .NicolaouB
  249162. JACSCACarbohyrate Chemistry
  249163. Lewis Acid Mediated Glycosylation
  249164. GlycosideI
  249165. 21276N
  249166. 2/28/96VNTotal Synthesis of Sulfated Le-x and Le-a Type Oligosacharide Selectin LigandsW
  249167. 1993X
  249168. 8843Y
  249169. R. L. FunkB
  249170. C]Ireland Claisen Rearrangement
  249171. Enolate
  249172. Weinreb Amide
  249173. Ester
  249174. Annulation (cyclic enol phosphates)I
  249175. 21277N
  249176. 2/28/96V(Claisen Rearrangement of Enol PhosphatesW
  249177. 1993X
  249178. 8847Y
  249179. R. L. FunkB
  249180. JACSC:Annulation
  249181. Titanium tetrachloride
  249182. Unsaturated Keto Esters
  249183. 21278N
  249184. 2/28/96VoTitanium-Mediated Cyclizations of B-Keto Esters with Acetals:  A Convenient Route to 2-CarbalkoxycycloalkenonesW
  249185. 1993X
  249186. 8849Y
  249187. D. L. Comins B
  249188. JACSC-Zinc Enolate
  249189. Pyridinium Salt
  249190. Chiral AuxillaryI
  249191. 21279N
  249192. 2/28/96V*Asymmetric Synthesis of (-)-PorantheridineW
  249193. 1993X
  249194. 8851Y
  249195. A    E. SuarezB
  249196. JACSC1Hypervalent Iodine
  249197. Iodosylbenzene
  249198. TetrahydrofuranI
  249199. 21280N
  249200. 2/28/96VhFragmentation of Carbohydrate Anomeric Alkoxy Radicals.  Tandem b-Fragmentation-Cyclization of Alcohols W
  249201. 1993X
  249202. 8865Y
  249203. E. J. CoreyB
  249204. JACSC-Samarium Iodide
  249205. Annulation
  249206. Aldol Cyclization
  249207. 21281N
  249208. 2/28/96V7Total Synthesis of (
  249209. )-Paeoniflorigenin and PaeoniforinW
  249210. 1993X
  249211. 8871Y
  249212. E. J. Corey
  249213. JACSC
  249214. Manganese
  249215. Annulation
  249216. 21282N
  249217. 2/28/96V7Total Synthesis of (
  249218. )-Paeoniflorigenin and PaeoniforinW
  249219. 1993X
  249220. 8871Y
  249221. E. J. Corey
  249222. JACSC5Carbohydrate Chemistry
  249223. Glycoside Coupling
  249224. Lewis Acid
  249225. K) See also: Y. Watanabe Synlett 1993,115.
  249226. 21283N
  249227. 2/28/96V8Total Synthesis of (
  249228. )-Paeoniflorigenin and PaeoniflorinW
  249229. 1993X
  249230. 8871Y
  249231. E. J. Corey B
  249232. JACSCXLewis Acid
  249233. Biomimetic Cyclization
  249234. Steriod Chemistry
  249235. Fluorine Chemistry
  249236. Cyclopropanation
  249237. KmAlso noteworthy, CBS reduction, conversion of epoxide to a fluorohydrin and Li reduction of homoallylic dieneM
  249238. 21284N
  249239. 2/28/96V
  249240. Enantioselective Total Synthesis of Oleanolic Acid, Erythrodiol, b-Amyrin, and Other Pentacyclic Triterpenes from a Common IntermediateW
  249241. 1993X
  249242. 8873Y
  249243. E. NakamuraB
  249244. JACSC+Chromium Carbene Complex
  249245. Enolate
  249246. AlkylationI
  249247. 21285N
  249248. 2/28/96
  249249. VfAcyclic Stereocontrol in Fischer Carbene Chemistry by Syn Selective Michael Addition/Trapping SequenceW
  249250. 1993X
  249251. 9015Y
  249252. I. KuwajimaB
  249253. JACSC+Silicon Chemistry
  249254. Carbanion
  249255. Allyl Sulfides
  249256. 21286N
  249257. 2/28/96VFRegiochemically and Stereochemically Defined Synthesis of AllylsilanesW
  249258. 1993X
  249259. 9021Y
  249260. D. L. BogerB
  249261. JACSC-CC-1065
  249262. Indole Synthesis
  249263. cyclopropane
  249264. enamineI
  249265. 21287N
  249266. 2/28/96VNTotal Synthesis and Preliminary Evaluation of (+)- and ent-(-)- Duocarmycin SAW
  249267. 1993X
  249268. 9025Y
  249269. L. S. Hegedus B
  249270. JACSCbChromium Amino Carbene Complex
  249271. Photochemistry
  249272. Polymer Supported Peptide Synthesis
  249273. Merrifield ResinI
  249274. 21288N
  249275. 2/28/96V
  249276. Solid-Phase, Solution, and Segment Condensation Peptide Synthesis Incorporating Chromium Carbene Complex-Derived Nonproteinogenic (Unnatural) Amino Acid Fragments  W
  249277. 1993X
  249278. 9037Y
  249279. L. S. LiebeskindB
  249280. JACSC9Palladium Coupling
  249281. Copper Iodide Catalyst
  249282. Organostannane
  249283. 21289N
  249284. 2/28/96
  249285. V+4,4'-Bi(cyclobutene-1,2-diones):  BiquarylsW
  249286. 1993X
  249287. 9048Y
  249288. B. H. LipshutzB
  249289. JACSC
  249290. Cuprates
  249291. Aryl Lithium SpeciesI
  249292. 21290N
  249293. 2/28/96VzSynthesis of Unsymmetrical Biaryls via Kinetic Higher Order Cyanocuprates:  Scope, Limitations, and Spectroscopic InsightsW
  249294. 9276Y
  249295. B. H. LipshutzB
  249296. JACSI
  249297. 21291N
  249298. 2/28/96V9The Role of TMSCl in Gilman Cuprate 1,4-Addtion ReactionsW
  249299. 1993X
  249300. 9283Y
  249301. L. O. OvermanB
  249302. JACSC@Palladium Catalyzed Carbonylation
  249303. Triphenylarsine
  249304. OrganostannaneI
  249305. 21292N
  249306. 2/28/96V2Enantioselective Total Synthesis of (-)-StrychnineW
  249307. 1993X
  249308. 9293Y
  249309. L. O. OvermanB
  249310. JACSC<Aza Cope Mannich Cyclization
  249311. Iminium Ion [3+3] RearrangementI
  249312. 21293N
  249313. 2/28/96V2Enantioselective Total Synthesis of (-)-StrychnineW
  249314. 1993X
  249315. 9293Y
  249316. L. E. OvermanB
  249317. JACS C/Epoxide Ring Opening
  249318. Allyl Stannane
  249319. Lewis Acid
  249320. 21294N
  249321. 2/28/96
  249322. V8Enantioselective Total Synthesis of (+)-IsolaurepinnacinW
  249323. 1993X
  249324. 9305Y
  249325. L. E. OvermanB
  249326. JACSC@Oxonium Ion
  249327. Vinyl Silane
  249328. Lewis Acid Promoted Cyclization
  249329. OxepeneI
  249330. 21295N
  249331. 2/28/96V8Enantioselective Total Synthesis of (+)-IsolaurepinnacinW
  249332. 1993X
  249333. 9305Y
  249334. R. M. WilliamsB
  249335. JACSC+Palladium Catalyzed Cyclization
  249336. Annulation
  249337. 21296N
  249338. 2/28/96V7Stereocontrolled Total Synthesis of (+)-Paraherquamide W
  249339. 1993X
  249340. 9323Y
  249341. R. M. WilliamsB
  249342. JACSC1Alkylation of Gramine Derivative
  249343. Ketoester
  249344. IndoleI
  249345. 21297N
  249346. 2/28/96V6Stereocontrolled Total Synthesis of (+)-ParaherquamideW
  249347. 1993X
  249348. 9323Y
  249349. R. M. WilliamsB
  249350. JACSC1Intramolecular SN2' Alklyation
  249351. Annulation
  249352. EnolateI
  249353. 21298N
  249354. 2/28/96V6Stereocontrolled Total Synthesis of (+)-ParaherquamideW
  249355. 1993X
  249356. 9323Y
  249357. E. J. CoreyB
  249358. JACSC.Claisen Rearrangement
  249359. Allyl Phenol
  249360. Allyl EtherI
  249361. 21299N
  249362. 2/28/96V.Enantioselective Total Synthesis of MiroestrolW
  249363. 1993X
  249364. 9327Y
  249365. E. J. CoreyB
  249366. JACSClCationic Olefin Cyclization
  249367. Lewis Acid Catalyzed Diels-Alder Reaction
  249368. Annulation
  249369. Palladium Coupling
  249370. StannaneI
  249371. KKSynthesis of the Starting Material was accomplished using a Stille couplingM
  249372. 21300N
  249373. 2/28/96V.Enantioselective Total Synthesis of MiroestrolW
  249374. 1992X
  249375. 9327Y
  249376. S. M. DanishefskyB
  249377. JACSCCTricarbonyl Synthesis 
  249378. Dess-Martin Periodinane Oxidation
  249379. Sulfoxide
  249380. 21301N
  249381. 2/28/96VZTotal Synthesis of Rapamycin via a Novel Titanium-Mediated Aldol Macrocyclization ReactionW
  249382. 1993X
  249383. 9345Y
  249384. S. J. DanishefskyB
  249385. JACSC0Macrocyclization
  249386. Aldol Reaction
  249387. Titanium EnolateI
  249388. 21302N
  249389. 2/28/96VZTotal Synthesis of Rapamycin via a Novel Titanium-Mediated Aldol Macrocyclization ReactionW
  249390. 1993X
  249391. 9345Y
  249392. P. Magnus
  249393. JACSC3Oxidation
  249394. Azide Synthesis
  249395. Allyl Stannane
  249396. Lewis AcidI
  249397. 21303N
  249398. 2/28/96
  249399. VsDirect N-Alkyl Azidonation of N,N-Dialkylarylamines with the Iodosylbenzene/Trimethylsilylazide Reagent CombinationW
  249400. 1993X
  249401. 9347Y
  249402. A    K. TakedaB
  249403. JACSC
  249404. Silicon ChemistryI
  249405. 21304N
  249406. 2/28/96V
  249407. Reaction of b-Heteroatom -Substituted a,b-Unsaturated Acylsilanes with Ketone Enolates:  A New [3+2] Annulation Based on Brook RearrangementW
  249408. 1993X
  249409. 9351Y
  249410. L. E. OvermanB
  249411. JACSC+Directed Metalation
  249412. Carbanion
  249413. OrganolithiumI
  249414. 21305N
  249415. 2/28/96V
  249416. Asymmetric Synthesis of Either Enantiomer of Opium Alkaliods and Morphinans.  Total Synthesis of (-)-and (+)-Dihydrocodeinone and (-)- and (+)-MorphineW
  249417. 1993X
  249418. 11028Y
  249419. L. E. OvermanB
  249420. JACSC>Allyl Silane
  249421. Lewis Acid
  249422. Iminium ion - Allylsilane Cyclization
  249423. 21306N
  249424. 2/28/96V
  249425. Asymmetric Synthesis of Either Enantiomer of Opium Alkaliods and Morphinans.  Total Synthesis of (-)-and (+)-Dihydrocodeinone and (-)- and (+)-MorphineW
  249426. 1993X
  249427. 11028Y
  249428. L. E. OvermanB
  249429. C:Heck Coupling
  249430. Palladium Catalyzed Cyclization 
  249431. Annulation
  249432. 21307N
  249433. 2/28/96V
  249434. Asymmetric Synthesis of Either Enantiomer of Opium Alkaliods and Morphinans.  Total Synthesis of (-)-and (+)-Dihydrocodeinone and (-)- and (+)-MorphineW
  249435. 1993X
  249436. 11028Y
  249437. C. R. JohnsonB
  249438. JACSC<Palladium Catalyzed Coupling Reaction
  249439. Boron 
  249440. Suzuki CouplingI
  249441. 21308N
  249442. 2/28/96V
  249443. A Two Step, Three Component Synthesis of PGE1:  Utilization of a-Iodoenones in Pd(0)-Catalyzed Cross Couplings of Organoboranes W
  249444. 1993X
  249445. 11014Y
  249446. C. R. JohnsonB
  249447. JACSCDVinyl Stannane
  249448. Higher Order Cuprate Addition
  249449. Conjugate Addtion
  249450. EnoneI
  249451. 21309N
  249452. 2/28/96V
  249453. A Two Step, Three Component Synthesis of PGE1:  Utilization of a-Iodoenones in Pd(0)-Catalyzed Cross Couplings of Organoboranes W
  249454. 1993X
  249455. 11014Y
  249456. G. E. KeckB    Tet. Let.C@Stannane
  249457. Chiral Titanium Lewis Acid Catalyst
  249458. Binaphthol Ligand
  249459. 21310N
  249460. 2/28/96
  249461. V]Catalytic Asymmetric Allylation (CAA) Reactions.  A New Enantioselective Allylation ProcedureW
  249462. 1993X
  249463. 7827Y
  249464. P. KnochelB    Tet. Let.C%Zinc Species
  249465. Cuprate
  249466. Radical CouplingI
  249467. 21311N
  249468. 2/28/96V
  249469. Stereoselective Synthesis of Polyfunctional Di- and Trisubstituted Cyclopentane Derivatives using a New Palladium Catalyzed Cyclization.W
  249470. 1993X
  249471. 7911Y
  249472. E. J. Corey B
  249473. JACSC3Asymmetric Catalytic Hydrogenation
  249474. DIPAMP SynthesisI
  249475. 21312N
  249476. 2/28/96VUA New Highly Enantioselective Synthetic Route to P-Chiral Phosphines and DiphosphinesW
  249477. 1993X
  249478. 11000Y
  249479. K. N. HoukB
  249480. JACSI
  249481. 21313N
  249482. 2/28/96V{Theory of Gas-Phase and Solution Stereoselectivites of Hydride Reductions of Cyclohexanone Derivatives by Silicon Hydrides W
  249483. 1993X
  249484. 10992Y
  249485. W. BauerB
  249486. JACSC!Organo Lithium Reagents
  249487. CarbanionI
  249488. 21314N
  249489. 2/28/96VzVinyllithium:  Dynamic Behavior in Tetrahydrofuran Solution and Comprehensive Analysis of NMR Spin-Spin Coupling Constants
  249490. 1993X
  249491. 10871Y
  249492. T. Cohen
  249493. JACSC
  249494. Cyclopropane
  249495. Sulfur Silicon Chemistry
  249496. Radical Anion
  249497. Carbanion
  249498. Flash Vacuum Pyrolysis
  249499. Annulation
  249500. Thermal Rearrangement
  249501. Carbene
  249502. 21315N
  249503. 2/28/96V
  249504. Stereocontrolled Double Ring Expansion of Fused Allylidenecyclopropanes.  A Novel Route to Hydroazulenes and Other Fused Bicyclic Systems  W
  249505. 1993X
  249506. 10754Y
  249507. A    P. GarnerB
  249508. JACSCFPhotochemistry
  249509. Cycloaddition
  249510. Oppolzer's Chiral Sultam
  249511. Azomethine YlideI
  249512. 21316N
  249513. 2/28/96VRThe Asymmetric Synthesis of (-)-Quinocarcin via 1,3-Dipolar Cycloadditive StrategyW
  249514. 1993X
  249515. 10742Y
  249516. A    P. GarnerB
  249517. JACSC1Wittig Olefination
  249518. Dihydroisoquinoline Synthesis
  249519. 21317N
  249520. 2/28/96VRThe Asymmetric Synthesis of (-)-Quinocarcin via 1,3-Dipolar Cycloadditive StrategyW
  249521. 1993X
  249522. 10742Y
  249523. L. E. OvermanB
  249524. JOCCTAnnulation
  249525. Allyl Silane
  249526. Amine Synthesis
  249527. Cationic Iminium Ion Cyclization
  249528.  Lewis AcidI
  249529. 21318N
  249530. 2/28/96
  249531. V[Simple Method for Controlling Stereoselection in Mannich Cyclization Reactions of AldehydesW
  249532. 1993X
  249533. 6947Y
  249534. L. E. OvermanB
  249535. JOCC=Palladium Catalyzed Cyclization
  249536. Annulation
  249537. Oxindole SynthesisI
  249538. 21319N
  249539. 2/28/96V
  249540. Catalytic Asymmetric Synthesis of Either Enantiomer of Physostigmine.  Formation of Quaternary Carbon Centers with High Enantioselection by Intramolecular Heck Reactions of (Z)-2-Butenanildes W
  249541. 1993X
  249542. 6949Y
  249543. G. MolanderB
  249544. JOC CJSamarium Iodide
  249545. Ketone Synthesis 
  249546. Annulation
  249547. Lanthanide Reductive CouplingI
  249548. 21320N
  249549. 2/28/96V
  249550. Intramolecular Nucleophilic Acyl Substitution Reactions of Halo-Substituted Esters and Lactones.  New Applications of  Organosamarium Reagents W
  249551. 1993X
  249552. 7216Y
  249553. J. R. FlackB
  249554. Tet. Lett.CFOrgano Stannane
  249555. Palladium  Coupling
  249556. Stille Reaction
  249557. Copper Co-catalystI
  249558. 21321N
  249559. 2/28/96VdStereospecific a-Alkoxystannane Couplings With Acyl Chlorides:  Total Synthesis of (+)-GoniofufuroneW
  249560. 1993X
  249561. 8007Y
  249562. Y. KishiB
  249563. Tet. Lett.C)Carbanion
  249564. Organo Lithium
  249565. Quaterary CentreI
  249566. 21322N
  249567. 2/28/96V]A Concise Synthesis of Enantiomerically Pure Taxane C-Ring via the[2,3] Wittig Rearrangement W
  249568. 1993X
  249569. 8047Y
  249570. D. BogerB
  249571. JACSCPInverse Demand Diels-Alder Reaction
  249572. Pyridine Synthesis
  249573. Elimination
  249574. DDQ OxidationI
  249575. 21323N
  249576. 2/28/96V!Total Synthesis of StreptonigroneW
  249577. 1993X
  249578. 10733Y
  249579. H. Yamamoto B
  249580. JACSCJChiral Acetal
  249581. Aluminum Reagents
  249582. Alkylation
  249583. Oxetane Ring Opening
  249584. Lewis AcidI
  249585. 21324N
  249586. 2/28/96VrHighly Diastereoselective Acetal Cleavages Using Novel Reagents Prepared from Organoaluminum and PentafluorophenolW
  249587. 1993X
  249588. 10695Y
  249589. 115 (23)
  249590. W. WulffB
  249591. JACSC
  249592. Chromium Carbene Complex
  249593. 21325N
  249594. 2/28/96V
  249595. Intramolcular Reactions of Fischer Carbene Complexes with Alkynes and a Mechanistic Study of the Interception  of Reactive Intermediates with Added AcetylenesW
  249596. 1993X
  249597. 10671Y
  249598. 115 (23)
  249599. P. BeakB
  249600. C"Benzamide
  249601. Organolithium
  249602. Carbanion
  249603. 21326N
  249604. 2/28/96V
  249605. Directed Lithiations:  The Effect of Varying Directing Group Orientation on Competitive Efficiencies for a Series of Tertiary Amide, Secondary Amide, and Alkoxide Directed Ortho LithiationsW
  249606. 1993X
  249607. 10628Y
  249608. 115 (23)
  249609. K. S. FeldmanB
  249610. JACSC
  249611. Annulation
  249612. 21327N
  249613. 2/28/96V
  249614. 2,2-Dihalovinylcyclopropanes as highly Diastereoselective Three Atom Addends in Phenylthio Radical Mediated Vinylcycopentane Synthesis W
  249615. 1993X
  249616. 11364Y    115 (24) 
  249617. C. KibayashiB
  249618. JACSCFOrganotin Reagent
  249619. Palladium Catalyzed Hydrostannylation
  249620. Vinyl StannaneI
  249621. 21328N
  249622. 2/28/96V
  249623. Highly Stereoselective Total Synthesis of (+)-Allopumiliotoxins 267A and 339A via Intramolecular Nickel(II)/Chromium (II)-Mediated CyclizationW
  249624. 1993X
  249625. 11393Y
  249626. 115 (24)
  249627. C. KibayashiB
  249628. JACSC7NiCl2 (cat)
  249629. CrCl2 (5 eq)
  249630. vinyl Iodide
  249631. Olefin Synthesis
  249632. 21329N
  249633. 2/28/96
  249634. Highly Stereoselective Total Synthesis of (+)-Allopumiliotoxins 267A and 339A via Intramolecular Nickel(II)/Chromium (II)-Mediated CyclizationW
  249635. 1993X
  249636. 11393Y
  249637. 115 (24)
  249638. D. L. BogerB
  249639. JACSC
  249640. Ullmann Macrocyclization
  249641. 21330N
  249642. 2/28/96V'Total Synthesis of  (+)-PiperazinomycinW
  249643. 1993X
  249644. 11426Y    115 (24) 
  249645. K. D. MoellerB
  249646. JACSC4Electrochemistry
  249647. Iminium Ion Cyclization
  249648. Annulation I
  249649. 21331N
  249650. 2/28/96VHAnodic Amide Oxidations:  Total Synthesis of (-)-A58365A and rac-A58365BW
  249651. 1993X
  249652. 11434Y
  249653. 115 (24)
  249654. D. A. Evans
  249655. JACSC$Aldol Condensation
  249656. Titanium Enolate
  249657. 21332N
  249658. 2/28/96V7Total Synthesis of the Macrolide Antibiotic Rutamycin BW
  249659. 1993X
  249660. 11446Y    115 (24) 
  249661. D. A. EvansB
  249662. JACSC<Boronic Acid
  249663. Vinyl Iodide
  249664. Palladium Coupling
  249665. Diene SynthesisI
  249666. 21333N
  249667. 2/28/96V7Total Synthesis of the Macrolide Antibiotic Rutamycin BW
  249668. 1993X
  249669. 11446Y
  249670. 115 (24)
  249671. T. LivinghouseB
  249672. C>Titanium Mediated Cyclization
  249673. Annulation
  249674. Pyrrolidine SynthesisI
  249675. 21334N
  249676. 2/28/96V
  249677. Synthetic Applications of Imidotitanium-Alkyne [2+2] Cycloadditions.  A Concise, Stereocontrolled Total Synthesis of the Antifungal Agent (+)-PreussinW
  249678. 1993X
  249679. 11485Y
  249680. 115 (24)
  249681. H. YamamotoB
  249682. JACSCFOrganosilicon Chemistry
  249683. Boron Lewis Acid Catalyst
  249684. Homoallylic AlcoholsI
  249685. 21335N
  249686. 2/28/96ViCatalytic Asymmetric Allylation Using a Chiral (Acyloxy)borane Complex as a Versitile Lewis Acid CatalystW
  249687. 1993X
  249688. 11490Y    115 (24 )
  249689. J. R. FlackB
  249690. JACSCaSpiroannulation
  249691. Steroid
  249692. Sulfur Chemistry
  249693. Ring Expansion
  249694. Hydrazone Carbanion Alkylation
  249695. AnnulationI
  249696. 21336N
  249697. 2/28/96V@Total Synthesis of the Spiro-o-benzoquinonefuran (-)-StypoldioneW
  249698. 1993X
  249699. 11606Y
  249700. 115 (24)
  249701. A    E. VedejsB
  249702. JACSC#Carbanion
  249703. Alkylation
  249704. Boron Chelate
  249705. 21337N
  249706. 2/28/96VOAsymmetric Transformations in Synthesis:  Chiral Amino Acid Enolate EquivalentsW
  249707. 1993X
  249708. 11612Y
  249709. 115 (24)
  249710. S. MuraiB
  249711. CEPhenols Synthesis
  249712. Annulation
  249713. Transition Metal Catalyzed CarbonylationI
  249714. 21338N
  249715. 2/28/96VrRuthenium-Catalyzed Reaction of 1,6-Diynes with Hydrosilanes and Carbon Monoxide:  A Third Way of Incorporating COW
  249716. 1993X
  249717. 11614Y    115 (24) 
  249718. M. F. SemmelhackB
  249719. JACSC2Bergman Cyclization
  249720. Radical
  249721. DNA Cleavage
  249722. Enediyne
  249723. 21339N
  249724. 2/28/96VbThe Enol-Keto Trigger in Initiating Arene Diradical Formation in Calicheamicin/Esperamicin AnalogsW
  249725. 1993X
  249726. 11618Y
  249727. 115 (24)
  249728. P. StangB
  249729. JACSC&Organostannane
  249730. Hypervalent Iodine
  249731. 21340N
  249732. 2/28/96V
  249733. Palladium(II) and Copper Cocatalyzed Coupling of Stereodefined Alkenyl(phenyl)iodonium Triflates and Unsaturated Tri-n-butylstannanesW
  249734. 1993X
  249735. 11626Y
  249736. 115 (24)
  249737. S. H. BertzB
  249738. JACSC
  249739. Organocopper
  249740. Cuprate
  249741. 21341N
  249742. 2/28/96VhPhenylcopper(I) and Diphenylcuprate(I):  Characterization of Aggregation States by 13C NMR Spectroscopy W
  249743. 1993X
  249744. 11640Y
  249745. 115 (24)
  249746. S. J. DanishefskyB
  249747. CDNitroso Diels-Alder Reaction
  249748. Photochemistry
  249749. Carbanion
  249750. Organolithium
  249751. 21342N
  249752. 2/28/96VpIntramolecular Cycloaddition Reactions of Dienyl Nitroso Compounds:  Application to the Synthesis of Mitomycin KW
  249753. 1993X
  249754. 12305Y
  249755. 115 (26)
  249756. S. J. DanishefskyB
  249757. JACSCHBarton Deoxygenation
  249758. Organostannane
  249759. Radical
  249760. Aziridine
  249761. Allylic Amine
  249762. TBTHI
  249763. 21343N
  249764. 2/28/96VpIntramolecular Cycloaddition Reactions of Dienyl Nitroso Compounds:  Application to the Synthesis of Mitomycin KW
  249765. 1993X
  249766. 12305Y
  249767. 115 (26)
  249768. I. RyuB
  249769. JACSCFSiloxycyclopropanes
  249770. 1,6-diketone
  249771. Homoenolate
  249772. Copper
  249773. Conjugate AdditionI
  249774. 21344N
  249775. 2/28/96Vqb-Copper(II) Ketones.  Generation, Coupling, and Highly Stereoselective Trapping by Electron-Deficient AcetylenesW
  249776. 1993X    12330
  249777. 115 (26)
  249778. A    K. S. LamB
  249779. JACSI
  249780. 21345N
  249781. 2/28/96V@Biosynthesis of Esperamicin A1, an Enediyne Antitumor AntibioticW
  249782. 1993X
  249783. 12340Y
  249784. 115 (26)
  249785. B. M. TrostB
  249786. JACSC
  249787. Annulation
  249788. Diene Synthesis
  249789. 21346
  249790. 2/28/96VL
  249791. Diastereoselective Cycloisomerizations of Enediynes via Palladium CatalysisW
  249792. 1993X
  249793. 12491Y
  249794. 115 (26)
  249795. S.L. BuchwaldB
  249796. JACSC"Chiral Titanium Catalyst
  249797. ReductionI
  249798. 21347N
  249799. 2/28/96VgAsymmetric Hydrogenation of Unfunctionalized Trisubstituted Olefins with a Chiral Titanocene Catalyst
  249800. 1993X
  249801. 12569Y
  249802. 115 (26)
  249803. E. J. CoreyB
  249804. JACSC1OsO4
  249805. Cinchona Alkaloids
  249806. Quinidine
  249807. Diol Synthesis
  249808. The two quinoline units (Ar) are located in parallel planes with one OsO4 bonded to a quinuclidine nitrogen (N*).  Styrene affords the dihydroxylation product with 97% ee and with an R configuration. M
  249809. 21348N
  249810. 2/28/96V
  249811. Rigid and Highly Enantioselective Catalyst for the Dihydroxylation of Olefins Using Osmium Tetroxide Clarifies the Orgin of EnantiospecificityW
  249812. 1993X
  249813. 12579Y
  249814. 115 (26)
  249815. P. Metz
  249816. JACSC7Intramolcular Diels-Alder
  249817. Base Catalyzed Isomerization
  249818. 21349N
  249819. 2/28/96
  249820. VfAn Enantioselective Approach to 3a-hydroxy-15-rippertene.  Construction of the Tetracyclic Ring SystemW
  249821. 1993X
  249822. 12595Y    115 (26) 
  249823. P. MetzB
  249824. JACSC
  249825. Photochemistry
  249826. RearrangementI
  249827. 21350N
  249828. 2/28/96VfAn Enantioselective Approach to 3a-hydroxy-15-rippertene.  Construction of the Tetracyclic Ring SystemW
  249829. 1993X
  249830. 12595Y
  249831. 115 (26)
  249832. S.L.SchreiberB
  249833. JACSC8Nickel Chloride
  249834. Chromium Chloride
  249835. Nozaki Kishi Reaction
  249836. 21351N
  249837. 2/28/96VATotal Synthesis of the Immunosuppressive Agent (-)-DiscodermolideW
  249838. 1993X
  249839. 12621Y    115 (26) 
  249840. S. L. SchreiberB
  249841. JACSC.Lithium Enolate
  249842. Diastereoselective Alkylation
  249843. 21352N
  249844. 2/28/96VATotal Synthesis of the Immunosuppressive Agent (-)-DiscodermolideW
  249845. 1993X
  249846. 12621Y
  249847. 115 (26)
  249848. B. H. LipshutzB
  249849. JACSC;Conjugate Addition
  249850. Higher Order Cyano Cuprate
  249851. Organocopper
  249852. 21353N
  249853. 2/28/96
  249854. Cyanocuprate-Catalyzed 1,4-Additions of Vinylic Zirconocenes Using A Zincate as an Organolithium Shuttle.  A New and Potentially Practical Approach to 3 Component CouplingsW
  249855. 1993X
  249856. 12625Y
  249857. 115 (26)
  249858. A    P. MagnusB
  249859. JACSC
  249860. Diradical
  249861.  AnnulationI
  249862. 21354N
  249863. 2/28/96V
  249864. Studies on Dynemicin.  A Nonradical Cycloaromatization Pathway for the Azabicyclo[7.3.1] Enediyne Core Structure Initiated by Thiolate AdditionW
  249865. 1993X
  249866. 12627Y
  249867. 115 (26)
  249868. A    P. MagnusB
  249869. JACSCOAnnulation
  249870. Lewis Acid Cyclization
  249871. Organoaluminum
  249872. Oxidation
  249873. Azide SynthesisI
  249874. 21355N
  249875. 2/28/96VrNew Trialkylsilyl Enol Ether Chemistry:  Intramolecular [2+2] Cyclizations of b-Amido Triisopropylsilyl Eol EthersW
  249876. 1993X
  249877. 12629Y
  249878. 115 (26)
  249879. I. KuwajimaB
  249880. JACSCLTitanium Lewis Acid
  249881. Zinc Chloride
  249882. Vinyl Sulfide
  249883. 1,6-Diketone
  249884. Aldol Reaction
  249885. 21356N
  249886. 2/28/96VO
  249887. A Novel Transformation Involving Selective Formation and Cleavage of C-C BondsW
  249888. 1993X
  249889. 12635Y
  249890. 115 (26)
  249891. J. W. GrissomB
  249892. CIBiradical Cyclization
  249893. Annulation 
  249894. Radical Cyclization
  249895. Bergman CyclizationI
  249896. 21357N
  249897. 2/28/96VKSynthetic Studies of the Tandem Enediyne-Mono- and Bis-Radical CyclizationsW
  249898. 1993X
  249899. 11744Y
  249900. 115 (25)
  249901. L. A. PaquetteB
  249902. JACSC8Anionic Oxy Cope Rearrangement
  249903. Vinyl Lithium 
  249904. AnnulationI
  249905. 21358N
  249906. 2/28/96VeDirect Elaboration of Complex Polyquinanes through 2-Fold Addition of Vinyl Anions to Squarate EstersW
  249907. 1993X
  249908. 12189Y
  249909. 115 (25)
  249910. S. E. DenmarkB
  249911. JACSCDOrganolithium
  249912. Phosphorus Stabilized Carbanion
  249913. Structural StudiesI
  249914. 21359N
  249915. 2/28/96Vj
  249916. Carbanion Hybridization of Thiophosphonamide-Stabilized Anions:  Remarkable Steric and Solvation Effects W
  249917. 1993X
  249918. 12195Y
  249919. 115 (25)
  249920. M. E. JungB
  249921. JACSC6Sharpless Epoxidation
  249922. Intramolecular Hydride Transfer
  249923. 21360N
  249924. 2/28/96V
  249925. Enantiospecific Synthesis of All Four Diastereomers of 2-Methyl-3-((trialkylsilyl)oxy)alkanals:  Facile Preparation of Aldols by Non-Aldol ChemistryW
  249926. 1993X
  249927. 12208Y
  249928. 115 (25)
  249929. K. B. SharplessB
  249930. JACSC+Asymmetric Diol Synthesis
  249931. Mechanistic StudyI
  249932. 21361N
  249933. 2/28/96V
  249934. On "The Orgin of High Enantioselectivity in the Dihydroxylation of Olefins Using Osmium Tetroxide and Cinchona Alkaloid Catalysts"W
  249935. 1993X
  249936. 12226Y
  249937. 115 (25)
  249938. C. H. HeathcockB
  249939. Lithium Enolate
  249940. Aldol ReactionI
  249941. 21362N
  249942. 2/28/96VfStudies on the Alkylation of Chiral Enolates:  Application toward theTotal Synthesis of Discoderolide W
  249943. 1993X
  249944. 5878Y
  249945. 58 (22)
  249946. C. H. HeathcockB
  249947. JOCC3Z Diene Synthesis
  249948. Titanium Reagent
  249949. Yamamoto Method
  249950. K%H. Yamamoto Tetrahedron 1987, 43, 723M
  249951. 21363N
  249952. 2/28/96VeStudies on the Alkylation of Chiral Enolates:  Application toward theTotal Synthesis of DiscoderolideW
  249953. 1993X
  249954. 5878Y
  249955. 58 (22)
  249956. J. R. FalckB
  249957. JACSC$Stille Coupling
  249958. Organostannanes
  249959. 21364N
  249960. 2/28/96VpStereospecific Palladium/Copper Cocatalyzed Cross-Coupling of a-Alkoxy- and a-Aminostannanes with Acyl ChloridesW
  249961. 1994X
  249962. 116 (1)
  249963. D. R. LangleyB
  249964. JACSI
  249965. 21365N
  249966. 2/28/96VYThe DNA-Esperamicin A1 Complex.  A Model Based on Solvated Molecular Dynamics SimulationsW
  249967. 1994X
  249968. 116 (1)
  249969. D. L. BogerB
  249970. JACSC
  249971. Inverse Electron Demand Diels-Alder Rxn
  249972. Cycloaddition
  249973. Pyrimidine Synthesis
  249974. Evans Tin Enolate Aldol Reaction
  249975. Amide Coupling Procedure
  249976. Desulfurization via Radical ChemistryI
  249977. 21366N
  249978. 2/28/96VDTotal Synthesis of (+)-P-3A, epi-(-)-P-3A, and (-)-Desacetamido P-3AW
  249979. 1994X
  249980. 116 (1)
  249981. P. J. StangB
  249982. JACSCAIntramolcular 1,5-C-H Insertion Reaction
  249983. Organostannane
  249984. Sulfone
  249985. 21367N
  249986. 2/28/96V
  249987. A New Method for the Synthesis of Cyclopentenones via the Tandem Michael Addition-Carbene Insertion Reaction of b-Ketoethynyl(phenyl)iodonium SaltsW
  249988. 1994X
  249989. 116 (1)
  249990. K. N. HoukB
  249991. JACSC$MM2 Calculations
  249992. Molecular MechanicsI
  249993. 21368N
  249994. 2/28/96V
  249995. Stereoselective Organometallic Reactions:  A Force Field Study of p-Allyl Intermediates in Nickel(0) Catalyszed Cycloadditions W
  249996. 1994X
  249997. 116 (1)
  249998. I. E. MarkoB
  249999. JACSC
  250000. Carbanion
  250001. Alkylation
  250002. 21369N
  250003. 2/28/96VdReverse Chemoselectivity in the Competitive Addition of Thallium Ate Complexes to Enones and KetonesW
  250004. 1994X
  250005. 116 (1)
  250006. A    N. KrauseB
  250007. JACSC
  250008. Cuprate
  250009. 21370N
  250010. 2/28/96VkNew Insights into the Structure of Oranocuprate p-Complexes by Determination of 13C, 13C Coupling ConstantsW
  250011. 1994X
  250012. 116 (1)
  250013. J. W. HerndonB
  250014. JACSC
  250015. Chromium Carbene Complex
  250016. 21371N
  250017. 2/28/96V
  250018. 1,5-Addition of Halogens and Pseudohalogens to Cyclopropylthiocarbene-Chromium Complexes:  A Stereocontrolled Synthesis of 1,4-Dihalo-1-alkene DerivativesW
  250019. 1994X
  250020. 116 (1)
  250021. P. BeakB
  250022. JACSC8Directed Lithiation
  250023. Carbanion
  250024. Metallation
  250025. Organolithium
  250026. 21372N
  250027. 2/28/96VuComplex Induced Proximity Effects: Evidence for a Complex on the Reaction Pathway of a'-Lithiation of a Benzylic UreaW
  250028. 1994X
  250029. 116 (1)
  250030. Y. YamamotoB
  250031. C.Radical Reaction
  250032. Organostannane
  250033. Allylstannane
  250034. 21373N
  250035. 2/28/96VAZinc Chloride as a Radical Initiator as Well as a Chelating AgentW
  250036. 1994X
  250037. 116 (1)
  250038. E. JacobsenB
  250039. JACSCFSchiff Base Metal Catalyzed Epoxidation
  250040. Aziridine
  250041. Manganese  
  250042. Copper
  250043. 21374N
  250044. 2/28/96V
  250045. Nonstereospecific Mechanisms in Asymmetric Addition to Alkenes Result in Enantiodifferentiation after the First Irreversible StepW
  250046. 1994X
  250047. 116 (1)
  250048. A    W. SmadjaB
  250049. SynlettI
  250050. ReviewM
  250051. 21375N
  250052. 2/28/96VcAcyclic Diastereofacial Selection in Intermolecular Racical Reactions Steric vs Electronic ControlsW
  250053. 1994X
  250054. no. 1
  250055. O. YonemitsuB
  250056. SynlettCJCarbohydrate Chemistry
  250057. Tetrahydropyran Synthesis
  250058. Tetrahydrofuran SynthesisI
  250059. 21376N
  250060. 2/28/96
  250061. Synthetic Studies of Halicondrin B, an Antitumor Polyether Macrolide Isolated From A Marine Sponge.  Stereoselective Synthesis of the C-1-C13 Fragment via Construction of the B acnd A Rings by Kinetically and Thermodynamically Controlled Intramolecular Michael Reactions 
  250062. 1994X
  250063. 38, 40,43, 46Y
  250064. no. 1
  250065. H. IshibashiB
  250066. SynlettCDPummerer Rearrangement
  250067. Sulfoxide
  250068. Electrophilic Aromatic SubstitutionI
  250069. 21377N
  250070. 2/28/96VKFirst Total Synthesis of the Benzopyranobenazepine Alkaloid (
  250071. )-ClavizepineW
  250072. 1994X
  250073. no. 1
  250074. J. SuffertB
  250075. SynlettCCPalladium Coupling
  250076. Bergman Reaction
  250077. Diradical
  250078. DNA Cleavage
  250079. EnediyneI
  250080. 21378N
  250081. 2/28/96ViThe Synthesis and Acid Induced Cycloaromatization of a Dienediyne Analog of Neocarzinostatine ChromophoreW
  250082. 1994X
  250083. no. 1
  250084. A    M. NakataB
  250085. SynlettC#Lewis Acid Catalyzed Cycloaddition
  250086. 21379N
  250087. 2/28/96VIThe Intramolecular Diels-Alder Reaction of a 14-Membered Diene-DienophileW
  250088. 1994X
  250089. J. BarluengaB
  250090. JOCC3Metal Halogen Exchange
  250091. Carbanion
  250092. Lithium
  250093. AlkylationI
  250094. 21380N
  250095. 2/28/96VUDirect Coupling of Functionalized Organolithium Compounds with Aryl and Vinyl HalidesW
  250096. 1993X
  250097. 5976Y
  250098. 58 (22)
  250099. G. A. MolanderB
  250100. JOCC\Enolate Alkylation
  250101. Titanium Catalyzed Michael Addition of AllylTrimethylsilane 
  250102. Oxonium Ion I
  250103. 21381N
  250104. 2/28/96V
  250105. Neighboring Group Participation in Lewis Acid Promoted [3+4] and [3+5] Annulations.  The Stereocontrolled Synthesis of Tricyclic EthersW
  250106. 1993X
  250107. 5931Y
  250108. 58 (22)
  250109. J. R. FalckB
  250110. JOCC3Alkylation
  250111. Sulfone
  250112. Annulation
  250113. Cyclization
  250114. ReductionI
  250115. 21382N
  250116. 2/28/96VbStereospecific Dehydrative Alkylation of Bis-Sulfones:  Synthesis of a Lesser Tea Tortix PheromoneW
  250117. 1993X
  250118. 5892Y
  250119. 58 (22)
  250120. D. KahneB
  250121. JACSCDEnediyne
  250122. Minor Groove of DNA
  250123. Bergman Cyclization
  250124. Diradical MechanismI
  250125. 21383N
  250126. 2/28/96VAStructural Characterization of a Calicheamicin-DNA Complex by NMRW
  250127. 1993X
  250128. 7954Y
  250129. 115 (18)
  250130. K. FukumotoB
  250131. Lithium Reduction
  250132. Annulation
  250133. 21384N
  250134. 2/28/96V
  250135. Synthesis of Poylcyclic Cyclobutane Derivatives by Tandem Intramolecular Michael Aldol Reaction under two Complementary Conditions:  TBSOTf-TEA and TMSI-HMDS  
  250136. 1993X
  250137. 8107Y
  250138. 115 (18)
  250139. A    P. MagnusB
  250140. JACSC
  250141. Pictet Spengler Condensation
  250142. Lawesson's Reagent
  250143. Intramolecular Michael Addtion
  250144. Sulfoxide
  250145. Pummerer Rearrangement to provide Cyclopropane
  250146. Annulation
  250147. Mercury (II) induced Cyclization
  250148. Wittig Reaction
  250149. 21385N
  250150. 2/28/96V8Synthesis of Strychnine and the Wieland-Gumlich AldehydeW
  250151. 1993X
  250152. 8116Y
  250153. 115 (18)
  250154. J. E. Leet
  250155. JACSC
  250156. Enediyne
  250157. DNA CleavageI
  250158. 21386N
  250159. 2/28/96VAChemistry and Structure Elucidation of the Kedarcidin ChromophoreW
  250160. 1993X
  250161. 8432Y
  250162. 115 (18)
  250163. T. FukuyamaB
  250164. JACSC:Amide Coupling procedure
  250165. Annulation
  250166. Heterocycle Synthesis
  250167. 21387N
  250168. 2/28/96V"Total Synthesis of (-)-Tantazole BW
  250169. 1993X
  250170. 8449Y
  250171. 115 (18)
  250172. Fukuyama, TB
  250173. Organolithium 
  250174. Carbanion
  250175. Cuprate
  250176. Wittig Reaction to afford an Allene
  250177. Asymmetric Mukaiyama Aldol Reaction
  250178. Triethylsilane Reduction
  250179. Takai Vinyl Iodide Synthesis
  250180. Palladium Coupling
  250181. Amide Coupling (BOP-Cl)
  250182. Beckmann Rearrangement
  250183. 21388N
  250184. 2/28/96V!Total Synthesis of (+)-LeinamycinW
  250185. 1993X
  250186. 8451Y
  250187. 115 (18)
  250188. Houk, K. N. B
  250189. JACSI
  250190. 21389N
  250191. 2/28/96VpThe Energetic Advantage of 5-exo Versus 6-endo Epoxide Openings:  A Preference Overwhelmed by Antibody CatalysisW
  250192. 1993X
  250193. 8453Y
  250194. 115 (18)
  250195. Sharpless, K. B. B
  250196. JACSC
  250197. Osmium Tetroxide
  250198. 21390N
  250199. 2/28/96V@Catalytic Asymmetric Dihydroxylation of Tetrasubstituted OlefinsW
  250200. 1993X
  250201. 8463Y
  250202. 115 (18)
  250203. Keck, G. E.B
  250204. JACSCLLewis Acid Catalyzed Addition of Allylstannane
  250205. organotin
  250206. Homoallylic AlcoholI
  250207. 21391N
  250208. 2/28/96V,Catalytic Asymmetric Allylation of AldehydesW
  250209. 1993X
  250210. 115 (18)
  250211. Danishefsky, S. J.B
  250212. CGCarbohydrate
  250213. Glycoside Coupling
  250214. Zinc Triflate
  250215. Lewis Acid
  250216. Glycal EpoxideI
  250217. 21392N
  250218. 2/28/96V
  250219. Application of the Gylcal Assembly Strategy to the Synthesis of a Branched Oligosaccharide:  The First Synthesis of a Complex SaponinW
  250220. 1993X
  250221. 8473Y
  250222. 115 (18)
  250223. Shibasaki, M.B
  250224. JACSC>Zinc copper Couple
  250225. Organozinc
  250226. Palladium Coupling
  250227. Vinyl Iodide
  250228. 21393N
  250229. 2/28/96VoCatalytic Asymmetric Synthesis of Benzylic Quaternary carbon Centers.  An Efficient Synthesis of (-)-EptazocineW
  250230. 1993X
  250231. 8477Y
  250232. 115 (18)
  250233. Shibasaki, M.
  250234. JACSC6Heck Reaction
  250235. Palladium Coupling
  250236. BINAP
  250237. Pictet SpenglerI
  250238. 21394N
  250239. 2/28/96VoCatalytic Asymmetric Synthesis of Benzylic Quaternary carbon Centers.  An Efficient Synthesis of (-)-EptazocineW
  250240. 1993X
  250241. 8477Y
  250242. 115 (18)
  250243. Takahashi, T.B
  250244. JACSC Grignard Reagent
  250245. Allylic Ethers
  250246. 21395N
  250247. 2/28/96VPZirconium Catalyzed Highly Regioselective Carbon-Carbon Bond Formation ReactionsW
  250248. 1993X
  250249. 8485Y
  250250. 115 (18)
  250251. Gilbertson, S. R.
  250252. JACSC
  250253. Organoiron Complexes
  250254. Iron 
  250255. 21396N
  250256. 2/28/96VcExo Selective Diels-Alder Reactions of a, b-Unsaturated Hexacarbonyl-Diiron Bridging Acyl ComplexesW
  250257. 8517Y
  250258. 115 (18)
  250259. Ireland, R. E.B
  250260. Ireland Claisen Rearrangement
  250261. DIBAL Reduction
  250262. Sharpless Epoxidation
  250263. Osmium Tetroxide
  250264. Cuprate
  250265. Hetero Diels-Alder Reaction
  250266. Dimethyldioxirane Oxidation
  250267. Radical Reduction with Phenyl Silane
  250268. Wittig Olefination
  250269. Chiral Crotyl Borane (H. C. Brown)
  250270. Hydroxyl Directed Hydrogenation
  250271. 21397N
  250272. 2/28/96V
  250273. Convergent Synthesis of Polyether Ionophore Antibiotics:  Synthesis of the Spiroketal and Tricyclic Glycal Segments of MonensinW
  250274. 1993X
  250275. 7152, 7166Y
  250276. 115 (16)
  250277. Krafft, M. E.B
  250278. JACSCGCobalt Hexacarbonyl Alkyne Complex 
  250279. Annulation
  250280. Cyclopentenone SynthesisI
  250281. -Rate acceleration with NMO over the thermal reaction.  
  250282. -Further rate enhancement in the presence of heteroatoms in the homopropargylic or bishomopropargylic position
  250283. - NMR characterization of an intermediate cobalt complexM
  250284. 21398N
  250285. 2/28/96V_Effect of Coordinating Ligands on the Pauson Khand Cycloaddition:  Trapping of an Intermediate W
  250286. 1993X
  250287. 7199Y
  250288. 115 (16)
  250289. Suzuki, A.B
  250290. JACSC
  250291. Hydroboration
  250292. Vinyl Sulfde
  250293. 21399N
  250294. 2/28/96V
  250295. Palladium(0) Catalyzed Thioboration of Terminal Alkynes with 9-(Alkylthio)-9-borabicyclo[3.3.1] nonane Derivatives:  Stereoselective Synthesis of Vinyl Sulfides via the Thioboration Cross Coupling SequenceW
  250296. 1993X
  250297. 7219Y
  250298. 115 (16)
  250299. Gawley, R. E.B
  250300. JACSC6Organolithium
  250301. Carbanion
  250302. Organostannane
  250303. Amine SynthesisI
  250304. 3KK-a-aminolithium species stable upto -40
  250305. C in the presence of TMEDA (45 min)M
  250306. 21400N
  250307. 2/28/96
  250308. 2-Lithio-N-methylpiperidine and 2-Lithio-N-methylpyrrolidine:  Configurationally and Chemically Stable Unchelated a-AminoorganolithiumsW
  250309. 1993X
  250310. 7515Y
  250311. 115 (16)
  250312. Molander, G. A.B
  250313. JACSCJChiral Secondary Alcohol
  250314. Enantioselective Borane Ketone Reduction
  250315. 1,4-DiolI
  250316. 21401N
  250317. 2/28/96V2Keto Borinate Reduction:  1,7-Asymmetric InductionW
  250318. 1993X
  250319. 7517Y
  250320. 115 (16)
  250321. Alper, HB
  250322. JACSC"Radical 
  250323. Carbonylation
  250324. Annulation
  250325. 21402N
  250326. 2/28/96V[The First Examples of Carbon Monoxide Trapping in a Manganese(III) Induced Oxidation SystemW
  250327. 1993X
  250328. 7543Y
  250329. 115 (16)
  250330. Wulff, W. D. B
  250331. JOCCAFischer Carbene Complexes
  250332. Enyne
  250333. Cyclobutane Synthesis
  250334. Annulation
  250335. 21403N
  250336. 2/28/96ViStereoselection in the Chromium mediated Intramolecular [2+2] Cycloadditions of Vinyl Ketenes and AlkenesW
  250337. 1993X
  250338. 5571Y
  250339. 58 (21)
  250340.  A    Luh, T-Y.B
  250341. JOCC9TBTH
  250342. Tetrahydropyran
  250343. Tetrahydrofuran
  250344. Cyclopropane
  250345. SiliconI
  250346. 21404N
  250347. 2/28/96
  250348. Tandem Radical [2+1] Cycloaddition.  Remarkable Silyl Substituent Effect on the Chemoselectivity of the Radical Cyclization ReactionsW
  250349. 1993X
  250350. 5574Y
  250351. 58 (21)
  250352. !A    Luh, T-Y.B
  250353. JOCCEGrignard
  250354. Acetal Ring Opening
  250355. Nickel Catalyzed Coupling
  250356. Dithioacetals
  250357. 21405N
  250358. 2/28/96VwDifferentiation of Contiguous Hydroxyl Goups by Regioselective Conversion of Acetonides into tert-ButylHydroxyl Ethers W
  250359. 1993X
  250360. 5576Y
  250361. 58 (21)
  250362. Rawal, V. H.B
  250363. JOCC-Strychnos Alkaloids
  250364. Palladium
  250365. Annulation
  250366. HeckI
  250367. 21406N
  250368. 2/28/96V
  250369. An Unexpected Heck Reaction.  Inversion of Olefin Geometry Facilitated by the Apparent Intramolecular Carbamate Chelation of the s-Palladium IntermediateW
  250370. 1993X
  250371. 5583Y
  250372. 58 (21)
  250373. Mascarenas, J. L.B
  250374. JOCCNSilicon Tether
  250375. Annulation
  250376. Thermal Cyclization
  250377. Silyl Baeyer Villiger Oxidation
  250378. 21407N
  250379. 2/28/96VFTemporary Tethering Strategies for [5+2] Pyrone Alkene Cycloadditions W
  250380. 1993X
  250381. 5585Y
  250382. 58 (21)
  250383. Seconi, G.B
  250384. Amine Synthesis
  250385. Organocuprate
  250386. 21408N
  250387. 2/28/96V[Electrophilic Amination of Higher Order Cuprates with N, O-Bis(trimethylsilyl)hydroxylamineW
  250388. 1993X
  250389. 5620Y
  250390. 58 (21)
  250391. %A    Beak, P.
  250392. JOCCEOrganolithium
  250393. Metallation
  250394. Carbanion
  250395. Alkylation
  250396. Aziridine
  250397. CyclopropaneI
  250398. 21409N
  250399. 2/28/96V
  250400. Intramolecular Cyclization of a-Lithioamine Synthetic Equivalents:  Convenient Syntheses of 3-, 5-, and 6-Membered Ring heterocyclic Nitrogen Compounds and Elaborations of 3-Membered Ring SystemsW
  250401. 1994X
  250402. 59 (2)
  250403. Marshall, J. E.B
  250404. JOCC,Homoallylic Alcohol
  250405. Carbanion
  250406. Organolithium
  250407. 21410N
  250408. 2/28/96V
  250409. Synthesis of the Pseudopterane 2,5-Furanocyclic Ring System by [2,3] Wittig Ring Contraction of Bridged Furan and Dihydrofuran Propargylic Ethers W
  250410. 1994X
  250411. 59 (2)
  250412. Burke, S. D.B
  250413. JOCCRCuprate
  250414. Allylic Mesylate
  250415. Grignard Reagent
  250416. Vinyl Iodide Synthesis
  250417. Silicon ChemistryI
  250418. Also Model System StudiedM
  250419. 21411N
  250420. 2/28/96
  250421. 'V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  250422. 1994X
  250423. 59 (2)
  250424. Burke, S. D.B
  250425. JOCC]Ireland Claisen [3,3] Rearrangement
  250426. Sigmatropic Rearrangement
  250427. Carboxylic Acid
  250428. TetrahydropyranI
  250429. 21412N
  250430. 2/28/96V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  250431. 1994X
  250432. 59 (2)
  250433. Burke, S. D.B
  250434. JOCCyIntramolecular Diels-Alder Cycloaddition
  250435. Retro Diels-Alder
  250436. Annulation
  250437. Palladium Catalyzed Stille Coupling
  250438. Organostannane
  250439. 21413N
  250440. 2/28/96V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  250441. 1994X
  250442. 59 (2)
  250443. Danishefsky, S. J. B
  250444. Palladium Coupling
  250445. Annulation
  250446. PALLADIUM, INTRAMOLECULAR HECK ARYLATION OF ENOL ETHERS, HEXAHYDRO OXAZINE, ARYL IODIDE, FR 900482I
  250447. 21414N
  250448. 2/28/96V_A Remarkable Stereochemical Inversion in Some Heck Arylation Reactions. A Mechanistic Proposal W
  250449. 1994X
  250450. 59 (2)
  250451. Vedejs, E.B
  250452. +CNLewis Acid Catalyzed Sigmatropic Rearrangement
  250453. Titanium Catalyst
  250454. Chiral Amine
  250455. 21415N
  250456. 2/28/96VGAza Claisen Rearrangements Initiated by Acid Catalyzed Michael AdditionW
  250457. 1994X
  250458. 116 (2)
  250459. Hayashi, T.B
  250460. JACSC9Olefin Synthesis
  250461. BINAP Catalyst
  250462. p-Allyl Palladium SpeciesI
  250463. 21416N
  250464. 2/28/96VfCatalytic Asymmetric Reduction of Allylic Esters with Formic Acid Catalyzed by Palladium MOP ComplexesW
  250465. 1994X
  250466. 116 (2)
  250467. -A    Dai, L-X.B
  250468. JOCC>Copper (II) co-catalyst
  250469. Wacker Oxidation
  250470. Morpholine Synthesis
  250471. 21417N
  250472. 2/28/96VYPalladium(II) Catalyzed Synthesis of Optically Active Tetrahydro-1,4-oxazine Derivatives W
  250473. 1993X
  250474. 4775Y
  250475. 58 (18)
  250476. Knochel, P.B
  250477. JOCCJAlkylation
  250478. Diethyl Zinc
  250479. Organocopper
  250480. Higher Order Cuprate
  250481. Transmetalation
  250482. 21418N
  250483. 2/28/96V\Cross Coupling  between Functionalized Alkylcopper Reagents and Functionalized Alkyl HalidesW
  250484. 1993X
  250485. 4718Y
  250486. 58 (18)
  250487. Yamamoto, Y.B
  250488. Diels-Alder Reaction
  250489. Chelation Controlled Addition Allyl Stannane
  250490. Titanium Chloride Catalyst
  250491. Homoallylic Alcohol Synthesis
  250492. Ph3As and Ph3Sb
  250493. 21419N
  250494. 2/28/96VTMediation of the Reactivity of the Strong Lewis Acid TiCl4 by Complexation with XPh3W
  250495. 1993X
  250496. 4783Y
  250497. 58 (18)
  250498. Weinreb, S. M.B
  250499. JOCCiLewis Acid Catalyzed Cyclization
  250500. Vinyl Silane N-sulfonyliminium Ion Ring Closure
  250501. Aminocyclitol Synthesis
  250502. 21420N
  250503. 2/28/96V6An Approach to the Total Synthesis of (+)-LycoricidineW
  250504. 1993X
  250505. 4823Y
  250506. 58 (18)
  250507. Weinreb, S. M.B
  250508. JOCC>Heck Coupling
  250509. Palladium Catalyzed Annulation
  250510. Thallium Acetate
  250511. HKvanti elimination of PdH
  250512. REVIEW: Heck, R. F.; In Comprehensive Organic Synthesis: Trost, B. M., Ed.1991; Vol. 1, p 833.M
  250513. 21421N
  250514. 2/28/96V6An Approach to the Total Synthesis of (+)-LycoricidineW
  250515. 1993X
  250516. 4823Y
  250517. 58 (18)
  250518. Scott, W. J.B
  250519. Grignard Reagent
  250520. Zinc Reagent
  250521. 21422N
  250522. 2/28/96
  250523. 2VPNickel Mediated Cross-Coupling of Unactivated Neopentyl Iodides with OrganozincsW
  250524. 1993X
  250525. 4866Y
  250526. 58 (18)
  250527. Harada, T.B
  250528. JOCC+Zinc Reagent
  250529. Palladium Coupling
  250530. Alkylation
  250531. 21423N
  250532. 2/28/96V
  250533. Reactions of 1,1-Dihaloalkenes with Triorganozincates:  A Novel Method for the Preparation of Alkenylzinc Species Associated with Carbon-Carbon Bond Formation  W
  250534. 1993X
  250535. 4897Y
  250536. 58 (18)
  250537. Weinreb, S. M.B
  250538. JOCCgIntramolecular Dipolar [3+2] Cycloaddition
  250539. Azomethine Ylide
  250540. Aziridine
  250541. Annulation
  250542. Flash Vacuum PyrolysisI
  250543. 21424N
  250544. 2/28/96VSDevelopment of a Strategy for the Synthesis of the Unusual Marine Alkaloid Sarain AW
  250545. 1993X
  250546. 4945Y
  250547. 58 (18)
  250548. Weinreb, S. M. B
  250549. JOCCyIntramolecular Allyl Silane N-tosyliminium Ion Cyclization
  250550. Ferric Chloride Lewis Acid
  250551. Annulation
  250552. Silicon Chemistry
  250553. AminolI
  250554. 21425N
  250555. 2/28/96VSDevelopment of a Strategy for the Synthesis of the Unusual Marine Alkaloid Sarain AW
  250556. 1993X
  250557. 4945Y
  250558. 58 (18)
  250559. Paquette, L. A.B
  250560. 6C;Anionic Oxy Cope
  250561. Oxidation
  250562. Vinyl Cerium Addition to Ketone
  250563. 21426N
  250564. 2/28/96V
  250565. Synthetic Equivalents of the Taxol C, D Ring System.  Examination of Nucleophilic Bicyclic Oxetanes and Less Strained Acetonide EquivalentsW
  250566. 1993X
  250567. 4952, 4963Y
  250568. 58 (18)
  250569. Giuliano, R. M.B
  250570. Annulation
  250571. [4+2] Cycloaddition
  250572. 21427N
  250573. 2/28/96VuDiastereofacial Selectivity of the Diels-Alder Reactions of Carbohydrate Derived Dienes and Their Carbocyclic AnalogsW
  250574. 1993X
  250575. 4979Y
  250576. 58 (18)
  250577. Curran, D. P.B
  250578. JOCC)Samarium Iodide Reduction
  250579. Radical Anion
  250580. 21428N
  250581. 2/28/96VOAdditive and Solvent Effects on SmI2 Reductions:  The Effects of Water and DMPUW
  250582. 1993X
  250583. 5008Y
  250584. 58 (18)
  250585. Rappoprt, H.B
  250586. JOCC1Annulation
  250587. Potassium Enolate
  250588. Aminoester SynthesisI
  250589. 21429N
  250590. 2/28/96V
  250591. Chirospecific Synthesis of (1S,3R)-1-Amino-3-(hydroxymethyl)cyclopentane,  a Precursor for Carbocyclic Nucleoside Synthesis.  Intramolecular Aziridine CyclizationsW
  250592. 1993X
  250593. 5019Y
  250594. 58 (18)
  250595. Larock, R. C. B
  250596. 21430N
  250597. 2/28/96V`Palladium Catalyzed Annulation of 1,4-Dienes Using Ortho-Functionallity-Substituted Aryl HalidesW
  250598. 1993X
  250599. 4509Y
  250600. 58 (17)
  250601. ;A    Kim, Y-H.B
  250602. JOCC)Enantioselective Reduction
  250603. Boron Hydride
  250604. 21431N
  250605. 2/28/96VxStereocontrolled Catalytic Asymmetric Reduction of Ketones with Oxazaborolidines Derived from New Chiral Amino Alcohols W
  250606. 1993X
  250607. 4511Y
  250608. 58 (17)
  250609. Larock, R. C.B
  250610. IodobenzaldehydeI
  250611. 21432N
  250612. 2/28/96VMSynthesis of Indenones via Palladium Catalyzed Annulation of Internal AlkynesW
  250613. 1993X
  250614. 4579Y
  250615. 58 (17)
  250616. Overman, L. E.B
  250617. Aza Cope Mannich Rearrangement
  250618. Lewis Acid
  250619. Iminium Ion Cyclization
  250620. Red-Al Reduction
  250621. Pictet Spengler Reaction
  250622. Osmium Tetroxide Oxidation of Si Enol Ether
  250623. 21433N
  250624. 2/28/96V
  250625. Total Synthesis of Amaryllidaceae Alkaloids of the 5,11-Methanomorphanthridine Type.  Efficient Total Synthesis of (-)-Pancracine and (
  250626. )-Pancracine.W
  250627. 1993X
  250628. 4662Y
  250629. 58 (17)
  250630. Rajanbabu, T. V.
  250631. Nugent,W. A.B
  250632. JACSC+Titanium Complex
  250633. Deoxygenation of Epoxide
  250634. UK6inter- and intramolecular trapping of radical species.M
  250635. 21434N
  250636. 2/28/96V
  250637. Selective Generation of Free Radicals from Epoxides using a Transition Metal Radical.  A Powerful New Tool for Organic SynthesisW
  250638. 1994X
  250639. 116 (3)
  250640. Suzuki, K.B
  250641. JACSCNC-Glycoside coupling
  250642. Tetrahydrofuran Synthesis
  250643. Organosilane
  250644. Silver PerchlorateI
  250645. 21435N
  250646. 2/28/96V#Total Synthesis of the GilvocarcinsW
  250647. 1994X
  250648. 1004Y
  250649. 116 (3)
  250650. Suzuki, K.B
  250651. JACSC6Benzyne 
  250652. Diels-Alder Cycloaddition
  250653. Naphthol Synthesis
  250654. 21436N
  250655. 2/28/96V#Total Synthesis of the GilvocarcinsW
  250656. 1994X
  250657. 1004Y
  250658. 116 (3)
  250659. Suzuki, K.B
  250660. JACSC(Heck Coupling
  250661. Palladium
  250662. Biaryl coupling
  250663. 21437N
  250664. 2/28/96V#Total Synthesis of the GilvocarcinsW
  250665. 1994X
  250666. 1004Y
  250667. 116 (3)
  250668. Kuwajima, IB
  250669. Lewis Acid
  250670. Amine Synthesis
  250671. 21438N
  250672. 2/28/96
  250673. BVUHighly Stereoselective Ene Reaction of Aldimines with 2-(Alkylthio)allyl Silyl EthersW
  250674. 1994X
  250675. 59 (3)
  250676. Hoye, T. R.B
  250677. 21439N
  250678. 2/28/96VsEnolate and Other Carbon Nucleophile Alkylation Reactions Using 1,2-Cyclic Sulfates as Terminal Epoxide EquivalentsW
  250679. 1994X
  250680. 59 (3)
  250681. Whitesell, J., K.B
  250682. JOCC)Dialkyl Zinc Reagent
  250683. Chlorosulfite Ester
  250684. 21440N
  250685. 2/28/96VZAsymmetric Synthesis of Chiral Sulfinate Esters and Sulfoxides.  Synthesis of SulforaphaneW
  250686. 1994X
  250687. 59 (3)
  250688. Barluenga, J.B
  250689. JOCC7Bromine Lithium Exchange
  250690. Organostannane
  250691. Silyl MigrationI
  250692. 21441N
  250693. 2/28/96V
  250694. Preparation and Reactivity of New b-Nitrogen Functionalized Vinylic Organolithium Compounds from Secondary Aliphatic Allylamines W
  250695. 1994X
  250696. 59 (3)
  250697. Hawkins, J. M.B
  250698. JOCC>Michael Addition
  250699. Lithium Enolate
  250700. Alkylation
  250701. b-Lactam SynthesisI
  250702. 21442N
  250703. 2/28/96VHAsymmetric Synthesis of Erythro and Threo a-Substituted b-Amino Esters  W
  250704. 1994X
  250705. 59 (3)
  250706. GA    Anaya, J.B
  250707. Angew. Chem. Int. Ed. Engl. C;Radical Cyclization
  250708. Annulation
  250709. Dithiane
  250710. b-Lactam Synthesis
  250711. Chemical HighlightsM
  250712. 21443N
  250713. 2/28/96W
  250714. 1993X
  250715. Yamakawa, K. B
  250716. Chem. Pharm. Bull.CDTitanium Tetrachloride
  250717. Allylsilane Aldehyde Condensation
  250718. Annulation
  250719. Chemical HighlightsM
  250720. 21444N
  250721. 2/28/96W
  250722. 1993X
  250723. Iwao, M.
  250724. Watanabe, M.B
  250725. HeterocyclesCSStille Palladium Catalyzed Coupling
  250726. Indole Synthesis
  250727. Benzyne Cyclization
  250728. AnnulationI
  250729. Chemical HighlightsM
  250730. 21445N
  250731. 2/28/96W
  250732. 1993X
  250733. 1483Y
  250734. JA    Stork, G.B
  250735. TLCYCationic Polyene Cyclization
  250736. Lewis Acid
  250737. Annulation
  250738. Radical Reduction
  250739. Epoxide Ring OpeningI
  250740. 21446N
  250741. 2/28/96VyRegiospecificty in the Cyclization of 6-(1-Hydroxyalkyl) Geraniol Derivatives.  A Simple Route to the Taxol A Ring SystemW
  250742. 1994X
  250743. 1481Y
  250744. 35 (10)
  250745. Burke, S. D.B
  250746. TLC[Acetal Initiated Vinlysilane Terminated Polyene Cationic Cyclization
  250747. Annulation
  250748. Lewis Acid
  250749. 21447N
  250750. 2/28/96
  250751. KV\Enantioselective Synthesis of Nagilactone F Via Vinylsilane Terminated Cationic Cyclization W
  250752. 1994X
  250753. 1503Y
  250754. 35 (10)
  250755. Kise, N.B
  250756. TLC2Zinc Reagent
  250757. Lewis Acid
  250758. Reformatsky Reagents
  250759. ImineI
  250760. 21448N
  250761. 2/28/96V
  250762. Reaction of N-Acyl-a-methoxyamines with Organozinc Reagents.  A Convenient Method for the Synthesis of Homoallylamines and b-Amino EstersW
  250763. 1994X
  250764. 1561Y
  250765. 35 (10)
  250766. Hodgson, D. M.B
  250767. TLC,Annulation
  250768. Chromium Chloride
  250769. Nickel ChlorideI
  250770. 21449N
  250771. 2/28/96VjChromium (II) Mediated Nickel (II) Catalyzed Cylclisations of (Iodoaryl)- Substituted Alkynes and AlkynalsW
  250772. 1994X
  250773. 1601Y
  250774. 35 (10)
  250775. Shioiri, T. B
  250776. SynlettC.Homologation of Aryl Alkyl Ketones to Alkynes
  250777. 21450N
  250778. 2/28/96V
  250779. 1.  Extension of the Colvin Rearrangement Using Trimethylsilyldiazomethane.  A New Synthesis of Alkynes        2.  A New Synthesis of Aldehydes from Ketones Utlilizing TrimethylsilyldiazomethaneW
  250780. 1994X
  250781. 107, 109Y
  250782. no. 2
  250783. Whitby, R. J.B
  250784. Synlett
  250785. Annulation
  250786. Enynes
  250787. 21451N
  250788. 2/28/96VnConvergent Synthesis of Aminobicyclo[3.3.0]octenes Using Zirconium Chemistry.  An Unusual Anti 1,3-Amine ShiftW
  250789. 1994X
  250790. no. 2
  250791. Laschat, S.B
  250792. SynlettC
  250793. Diels-Alder
  250794. 21452N
  250795. 2/28/96V
  250796. Intramolecular Hetero-Diels-Alder Reaction of Prolinol-Derived N-Arylamines Lewis Acid Dependent Reversal of the Diastereoselectivity W
  250797. 1994X
  250798. no. 2
  250799. Knolker, H-J.B
  250800. SynlettCAAnnulation
  250801. Silicon Chemistry
  250802. Lewis Acid
  250803. Baeyer-Villiger OxidationI
  250804. 21453N
  250805. 2/28/96V
  250806. [3+2] Cycloaddition of Allylsilanes, Part 5.  Synthesis of Bicyclo[3.3.0]octanes by Domino [3+2] Cycloadditions of Allysilanes and 3-Butyn-2-oneW
  250807. 1994X
  250808. Yamamoto, K.B
  250809. SynlettC1Silicon Chemistry
  250810. Palladium Chemistry
  250811. Annulation
  250812. 6-Endo CyclizationM
  250813. 21454N
  250814. 2/28/96VjA Novel Palladium (0) Catalyzed Cycloaddition of 2,7-Octadienyl Carbonate Containing an Allylsilane MoietyW
  250815. 1994X
  250816. no. 2
  250817. Kobayashi, S.B
  250818. Synlett
  250819. SCG Tin (II) Lewis Acid Mediated Asymmetric Aldol Reaction
  250820. Chiral Diamine
  250821. 21455N
  250822. 2/28/96VREnantioselective Synthesis of Both Diastereomers Including a-Alkoxy-b-methyl UnitsW
  250823. 1994X
  250824. no. 2
  250825. Suzuki, A.B
  250826. SynlettC
  250827. Boron Chemistry
  250828. 21456N
  250829. 2/28/96V
  250830. Synthesis of Allenes by Palladium Catalyzed Cross Coupling Reaction of Organoboron Compounds with Propargylic Carbonates:  Transmetallation of Organoboron Compounds with (Alkoxo)palladium Complexes Under Neutral Conditions W
  250831. 1994X
  250832. Garner, P.B
  250833. Oppolzer Camphor SultamI
  250834. 21457N
  250835. 2/28/96VVAuxiliary Controlled 1,3-Dipolar Cycloadditions of Chiral Stabilized Azomethine YlidesW
  250836. 1994X
  250837. 59 (1)
  250838. VA    Bosch, J.B
  250839. JOCCIMetallation
  250840. Carbanion
  250841. Organotin
  250842. Organolithium
  250843. Protecting Group for IndoleI
  250844. 21458N
  250845. 2/28/96V{Preparation and Reactions of 1-(tert-Butyldimethylsilyl)-3-lithioindole.  Regioselective Synthesis of 3-Substituted IndolesW
  250846. 1994X
  250847. 59 (1)
  250848. Reissig, H-U.B
  250849. JOCC=Carbanion
  250850. Organolithium
  250851. Aminoaldehyde
  250852. Aminoalcohol Synthesis
  250853. 21459N
  250854. 2/28/96VnStereoselective Synthesis of 3(2H)-Dihydrofuranones by Addition of Lithiated methoxyallene to Chiral AldehydesW
  250855. 1994X
  250856. 59 (1)
  250857. Fukumoto, K.B
  250858. Sharpless Epoxidation
  250859. Titanium Chemistry
  250860. Radical 
  250861. Rearrangement
  250862. Cyclobutanone Synthesis
  250863. Mercury Trifluoroacetata
  250864. Methyl Cerium Addition to KetoneI
  250865. 21460N
  250866. 2/28/96V
  250867. A Remarkable Substituent Effect on the Enantioselectivity of Tandem Asymmetric Epoxidation and Enantiospecific Ring Expansion of Cyclopropylidene Alcohols:  A New Enantioconrolled Synthesis of (-)-Debromoaplysin and (-)-AplysinW
  250868. 1994X
  250869. 59 (1)
  250870. Fukumoto, K.B
  250871. JOCC<Cyclopentenone Synthesis
  250872. Palladium Catalyzed Ring Expansion
  250873. 21461N
  250874. 2/28/96
  250875. A Remarkable Substituent Effect on the Enantioselectivity of Tandem Asymmetric Epoxidation and Enantiospecific Ring Expansion of Cyclopropylidene Alcohols:  A New Enantioconrolled Synthesis of (-)-Debromoaplysin and (-)-AplysinW
  250876. 1994X
  250877. 59 (1)
  250878. ZA    Kishi, Y.B
  250879. Nickel Chloride
  250880. Chromium Chloride
  250881. Takai reaction
  250882. Propargylic Alcohol Synthesis
  250883. Carbohydrate Chemistry
  250884. Acid Catalyzed Epoxide Ring Closure
  250885. Tetrahydropyran SynthesisI
  250886. 21462N
  250887. 2/28/96VuPreferred Conformation of C-Glycosides.  12.  Synthesis and Conformational Analysis of a,a-,a,b-,and b,b-C-TrehalosesW
  250888. 1994X
  250889. 59 (1)
  250890. Hatanaka, M.B
  250891. JOCC*Intramolcular Wittig Reaction 
  250892. Annulation
  250893. 21463N
  250894. 2/28/96V
  250895. Allylidenetriphenylphosphorane as a Bifunctional Reagent:  Synthesis of Cyclopentenones and a,b-Unsaturated Ketones with (3-(Alkoxycarbonyl)-2-ethoxy-2-propenylidene)triphenylphosphoraneW
  250896. 1994X
  250897. 59 (1)
  250898. \A    Hiroi, K.B
  250899. Alkylation
  250900. 21464N
  250901. 2/28/96
  250902. \VwThe Palladium Catalyzed Asymmetric a-Allylation of Carbonyl Compounds with Chiral Allyl Esters via Enamines and Imines W
  250903. 1994X
  250904. 59 (1)
  250905. Meyers, A. G.B
  250906. JACSC0Enediyne Antibiotics
  250907. Bergman Cyclization
  250908. RadicalI
  250909. 21465N
  250910. 2/28/96VdA Study of the Reaction of Calicheamicin g1 with Glutathione in thse Presence of Double Stranded DNAW
  250911. 1994X
  250912. 1255Y
  250913. 116 (4)
  250914. Sharpless, K. B.B
  250915. JACSI
  250916. 21466N
  250917. 2/28/96V{Toward an Understanding of the High Enantioselectivity in the Osmium Catalyzed Asymmetric Dihydroxylation (AD). 1. KineticsW
  250918. 1994X
  250919. 1278Y
  250920. 116 (4)
  250921. Yamamoto, H.B
  250922. JACSC
  250923. Chiral Boron ComplexI
  250924. 21467N
  250925. 2/28/96V\Br
  250926. nsted Acid Assisted Chiral Lewis Acid  (BLA) Catalyst for Asymmetric Diels-Alder ReactionW
  250927. 1994X
  250928. 1561Y
  250929. 116 (4)
  250930. Shibasaki, M.B
  250931. JACSI
  250932. 21468N
  250933. 2/28/96VYCatalytic Asymmetric Michael Reactions Promoted by a Lithium Free Lanthanum BINOL ComplexW
  250934. 1994X
  250935. 1569Y
  250936. 116 (4)
  250937. Nicolaou, K. C.B
  250938. McMurry Coupling
  250939. Diol Synthesis
  250940. Titanium  Chemistry
  250941. Sharpless Epoxidation
  250942. Shapiro Reaction
  250943. Vinyl Lithium Species
  250944. Carbanion
  250945. PCC Allylic Oxidation
  250946. AnnulationI
  250947. a) Review:  "Chemistry and Biology of Taxol"  Nicolaou, K. C. Angew. Chem. Int. Ed. Engl. 1994, 33, 15-44 
  250948. b) For a Total Synthesis of Taxol see:  Nicolaou, K. C. Nature, 1994, 367, 630
  250949. 21469N
  250950. 2/28/96V
  250951. Synthesis of Novel TaxoidsW
  250952. 1994X
  250953. 1591Y
  250954. 116 (4)
  250955. Holton, R. A.B
  250956. JACSC
  250957. Chan Rearrangement
  250958. Intramolecular Acylation
  250959. Aldol Reaction
  250960. Samarium Iodide Reduction
  250961. Chiral Davis Reagent
  250962. Oxidation of  Li Enolate with OxaziridineI
  250963. 21470N
  250964. 2/28/96VCFirst Total Synthesis of Taxol. 1.  Functionalization of the B RingW
  250965. 1994X
  250966. 1597Y
  250967. 116 (4)
  250968. Holton, R. A.B
  250969. JACSC
  250970. Dieckmann Cyclization to b-ketoester Annulation
  250971. Decarboxylation (PhSK)
  250972. Dehydration Burgess Reagent
  250973. Osmium Tetroxide
  250974. Oxetane Ring Synthesis
  250975. Oxidation of K Enolate to Hydroxy-ketone
  250976. Benzeneselenic Anhydride I
  250977. 21471N
  250978. 2/28/96
  250979. cVDFirst Total Synthesis of Taxol.  2.  Completion of the C and D RingsW
  250980. 1994X
  250981. 1599Y
  250982. 116 (4)
  250983. Pederson, S. F.B
  250984. JACSC9Diol Synthesis
  250985. Vanadium Chemistry
  250986. Aminoalcohol Synthesis
  250987. 21472N
  250988. 2/28/96V
  250989. Pinacol Cross Coupling of 2-[N-(Alkoxycarbonyl)amino] Aldehydes and Aliphatic Aldehydes by [V2Cl3(THF)6]2[Zn2Cl6].  Synthesis of syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-DiolsW
  250990. 1994X
  250991. 1316Y
  250992. 116 (4)
  250993. Aggarwal, V. K.B
  250994. Angew. Chem. Int. Ed. Engl. C
  250995. Asymmetric Deprotonation
  250996. ReviewM
  250997. 21473N
  250998. 2/28/96VkEnantioselective Transformations and Racemization Studies of Heteroatom Substituted Organolithium CompoundsW
  250999. 1994X
  251000. Nicolaou, K. C.B
  251001. Angew. Chem. Int. Ed. Engl.C,Enediyne Antiobiotic
  251002. DNA Cleavage
  251003. Diradical
  251004. 21474N
  251005. 2/28/96V
  251006. Calicheamicin:  A Rationally Designed Molecule with Extremely Potent and Selective DNA Cleaving Properties and Apoptosis Inducing ActivityW
  251007. 1994X
  251008. Aurrecoechea, J. M.B
  251009. gC%Annulation
  251010. Tertiary Alcohol SynthesisI
  251011. 21475N
  251012. 2/28/96V
  251013. Synthesis of Homopropargyl Cycloalkanols by Palladium Catalyzed Samarium Iodide Promoted Intramolecular Coupling of AlkynylEsters with Aldehydes and Ketones W
  251014. 1994X
  251015. 59 (4)
  251016. Denmark, S. E.B
  251017. 21476N
  251018. 2/28/96VqInvestigations on Transition State Geometry in the Lewis Acid - (Mukaiyama) and Fluoride Promoted Aldol ReactionsW
  251019. 1994X
  251020. 59 (4)
  251021. Shibasaki, M.B
  251022. JOCC<Intramolecular Chromium Complex      Cyclization
  251023. Annulation
  251024. 21477N
  251025. 2/28/96V
  251026. 1994X
  251027. 59 (4)
  251028. Paquette, L. A.B
  251029. Anionic Oxy Cope RearrangementI
  251030. 21478N
  251031. 2/28/96VoExploratory Synthetic Studies Involving the Tricyclo[9.3.3.0]tetradecane Ring System Peculiar to the Cyathins
  251032. 1994X
  251033. 59 (4)
  251034. Paquette, L. A.B
  251035. Radical Cyclization
  251036. AnnulationI
  251037. 21479N
  251038. 2/28/96
  251039. kVpExploratory Synthetic Studies Involving the Tricyclo[9.3.3.0]tetradecane Ring System Peculiar to the Cyathins
  251040. 1994X
  251041. 59 (4)
  251042. Tachibana, K.B
  251043. JOCC>Epoxide Ring Opening
  251044. Oxepane Ring Synthesis
  251045. 7-Endo CyclizationI
  251046. 21480N
  251047. 2/28/96V\Synthetic Studies toward Ciguatoxin.  Stereocontrolled Construction of the KLM Ring FragmentW
  251048. 1994X
  251049. 59 (4)
  251050. Malacria, M.B
  251051. JOCC1Annulation
  251052. [2+1] Radical Cyclization
  251053. CyclopropaneI
  251054. 21481N
  251055. 2/28/96V@A New Rare Example of Cyclopropanation in Free Radical ChemistryW
  251056. 1994X
  251057. 59 (4)
  251058. Shea, K. J.
  251059. TLC_Taxol Intermediate
  251060. Ireland Claisen Rearrangement
  251061. Organolithium
  251062. Carbanion 
  251063. Vinyl Lithium SpeciesI
  251064. 21482N
  251065. 2/28/96VbSynthesis of a C-1 Epi Taxinine Intermediate Using the Type 2 Intramolecular Diels-Alder Approach W
  251066. 1994X
  251067. 1317Y
  251068. 35 (9)
  251069. Trost, B. M.B
  251070. TLC1Annulation
  251071. Palladium Catalyzed Cyclization
  251072. EneyneI
  251073. 21483N
  251074. 2/28/96
  251075. oVOA Novel Cycloalkylation of 1,6- and 1,7-Enynes with Stabilized Pronucleophiles W
  251076. 1994X
  251077. 1361Y
  251078. 35 (9)
  251079. Whitby, R. J.B
  251080. TLC9Annulation
  251081. Insertion of Isocyanide into Zirconium ComplexI
  251082. 21484N
  251083. 2/28/96V8Synthesis of Cyclopentylamines using Zirconium ChemistryW
  251084. 1994X
  251085. 1445Y
  251086. 35 (9)
  251087. Molina, P.B
  251088. TLC=Aza Wittig
  251089. Electrocyclic Ring Closure
  251090. Pyridine Ring SynthesisI
  251091. 21485N
  251092. 2/28/96V@A Straightforward and Practical Formal Synthesis of LavendamycinX
  251093. 1453Y
  251094. 35 (9)
  251095. Enholm, E. J.B
  251096. TL CRSamarium Iodide
  251097. Annulation 
  251098. Aldol Reaction of Samarium Enolate
  251099. Radical CyclizationI
  251100. 21486N
  251101. 2/28/96VHSequential SmI2 Promoted One and Two Electron Reactions of Carbohyrates W
  251102. 1994X
  251103. 1627Y
  251104. 35 (11)
  251105. Crimmins, M.T. B
  251106. TLC.Silicon Tethered Photocyclization
  251107. Cyclobutane
  251108. 21487N
  251109. 2/28/96V;Siloxanes as Temporary Tethers in [2+2] PhotocycloadditionsW
  251110. 1994X
  251111. 1657Y
  251112. 35 (11)
  251113. Engler, T. A.B
  251114. TLC!Lewis Acid 
  251115. Stilbene
  251116. BenzoquinoneI
  251117. 21488N
  251118. 2/28/96V
  251119. Evaluation of a Synthetic Route to e-Viniferin Based on a New Method for the Stereoselective Preparation of 2,3-Diaryl-2,3-DihydrobenzofuransW
  251120. 1994X
  251121. 1661Y
  251122. 35 (11)
  251123. Knolker, H-J.B
  251124. TLC!Carbazole
  251125. Indole Ring Synthesis
  251126. Stiochiometric in Palladium(II)M
  251127. 21489N
  251128. 2/28/96V5Palladium Promoted Synthesis of a 7-DeoxyprekinamycinW
  251129. 1994X
  251130. 1695Y
  251131. 35 (11)
  251132. Kagan, H. B.B
  251133. TLC&Acid Chloride
  251134. a-Hyroxyketone SynthesisI
  251135. 21490N
  251136. 2/28/96VLSamarium Iodide in THP:  Preparation and some Reactions in Organic ChemistryW
  251137. 1994X
  251138. 1723Y
  251139. 35 (11)
  251140. Uemura, S.B
  251141. TLC Michael Type Conjugate Addition
  251142. KGNaBPh4 + AcOH  --->  Ph3B + PhH + NaOAc
  251143. Also see JOC 1995, 60 (4), 883M
  251144. 21491N
  251145. 2/28/96V
  251146. Antimony(III) Chloride as An Efficient Catalyst for Palladium Catalyzed Hydrophenylation of a,b-Unsaturated Ketones and AldehydesW
  251147. 1994X
  251148. 1739Y
  251149. 35 (11)
  251150. Bach, T.B
  251151. Angew. Chem. Int. Ed. Engl.
  251152. xCWSilyl Eonol Ether
  251153. Organotin
  251154. Organosilane
  251155. Chiral Lewis Acid Catalyst
  251156. Homoallylic AlcoholI
  251157. ReviewM
  251158. 21492N
  251159. 2/28/96VTCatalytic Enantioselective C-C Coupling -Allyl Transfer and Mukaiyama Aldol ReactionW
  251160. 1994X
  251161. 33 (4)
  251162. Meyers, A. G.B
  251163. JACSC
  251164. Enediyne AntibioticsI
  251165. 21493N
  251166. 2/28/96V
  251167. DNA Cleavage by Neocarzinostatin Chromophore.  Establishing the Intermediacy of Chromophore-Derived Cumulene and Biradical Species and Their Role in Sequence Specific Cleavage.W
  251168. 1994X
  251169. 1670Y
  251170. 116 (5)
  251171. Rychnovsky, S. D.B
  251172. JACSC
  251173. Organolithium 
  251174. Alkylation of a-Lithio-nitriles
  251175. Noyori Asymmetric Hydrogenation
  251176. Intramolecular Horner Emmons Wittig Rxn
  251177. CyanohydrinI
  251178. 21494N
  251179. 2/28/96V:Convegent Synthesis of the Polyene Macrolide (-)-RoxaticinW
  251180. 1994X
  251181. 1753Y
  251182. 116 (5)
  251183. Paquette, L. A.B
  251184. JACSC    Oxy-Cope I
  251185. 21495N
  251186. 2/28/96V
  251187. Tandem Cope Cope RearrangementsW
  251188. 1994X
  251189. 1776Y
  251190. 116 (5)
  251191. Baldwin, J. E. B
  251192. JACSC
  251193. Aldol Reaction
  251194. Lewis AcidI
  251195. 21496N
  251196. 2/28/96
  251197. |V5Total Synthesis of (+)-Lactacystin from (R)-GlutamateW
  251198. 1994X
  251199. 2139Y
  251200. 116 (5)
  251201. Roush, W. R.B
  251202. JACSC
  251203. Crotyl Borane
  251204. 21497N
  251205. 2/28/96V
  251206. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  251207. 1994X
  251208. 2151Y
  251209. 116 (5)
  251210. Roush, W. R.B
  251211. JACSC$Conjugate Addition
  251212. Grignard Reagent
  251213. 21498N
  251214. 2/28/96V
  251215. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  251216. 1994X
  251217. 2151Y
  251218. 116 (5)
  251219. Roush, W. R.B
  251220. JACSC
  251221. Triethyl Aluminum AlkylationI
  251222. 21499N
  251223. 2/28/96V
  251224. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  251225. 1994X
  251226. 2151Y
  251227. 116 (5)
  251228. Greene, A. E.B
  251229. JACSC/Cyclopentenone Synthesis
  251230. Cobalt Alkyne Complex I
  251231. 21500N
  251232. 2/28/96VtA Dual Function, Highly Efficient Chiral Chiral Controller for Stereoselective Intermolecular Pauson Khand ReactionsW
  251233. 1994X
  251234. 2153Y
  251235. 116 (5)
  251236. Vedejs, E.B
  251237. JACSI
  251238. 21501N
  251239. 2/28/96VaDeracemization via Highly Enantioselective Enolate Protonation Using a Chiral Aniline as the AcidW
  251240. 1994X
  251241. 2172Y
  251242. 116 (5)
  251243. Trost, B. M.B
  251244. JACSC(Palladium
  251245. Cyclopropane
  251246. Enyne
  251247. Annulation
  251248. 21502N
  251249. 2/28/96VJA Cycloaddition Approach to Cyclopentenes via Metalladienes as 4
  251250.  PartnersW
  251251. 1994X
  251252. 2183Y
  251253. 116 (5)
  251254. Marco-Contelles, J.B
  251255. JOCC&Annulation 
  251256. Alkyne
  251257. Tributyltin HydrideI
  251258. 21503N
  251259. 2/28/96VY6-endo-dig Free Radical Carbocyclizations:  A New Strategy for the Synthesis of CyclitolsW
  251260. 1994X
  251261. 1234Y
  251262. 59 (6)
  251263. Clive, D. L. J.B
  251264. JOCC5Annulation
  251265. Cobalt Chemistry
  251266. Cyclopentenone Synthesis
  251267. 21504N
  251268. 2/28/96VkFormation of Angularly Fused Triquinanes by Successive Use of the Pauson Khand Reaction and Radical ClosureW
  251269. 1994X
  251270. 1396Y
  251271. 59 (6)
  251272. Kise, N.B
  251273. JOCC?Electrochemistry
  251274. Annulation
  251275. Reduction
  251276. Radical Anion CyclizationI
  251277. 21505N
  251278. 2/28/96VJElectroreductive Intramolecular Coupling of Nonconjugated Aromatic KetonesW
  251279. 1994X
  251280. 1407Y
  251281. 59 (6)
  251282. A    Padwa, A.B
  251283. JOCC!Rhodium Carbene Complex
  251284. ReductionI
  251285. 21506N
  251286. 2/28/96V
  251287. Studies on the Intramolecular Cycloaddition Reaction of Mesoionics Derived From the Rhodium (II) Catalyzed Cyclization of DiazoimidesW
  251288. 1994X
  251289. 1418Y
  251290. 59 (6)
  251291. Lee, E.B
  251292. Annulation
  251293. Radical Anion
  251294. 21507N
  251295. 2/28/96V`Reductive Cyclization of Ketones Tethered to Activated Olefins Mediated by Magnesium in MethanolW
  251296. 1994X
  251297. 1428Y
  251298. 59 (6)
  251299. Marshall, J. A.B
  251300. Oxidation
  251301. Epoxidation
  251302. 21508N
  251303. 2/28/96V\Enantioselective Synthesis of Carbohydrate Precursors via 1,2:2,3-Bis-Epoxide Intermediates
  251304. 1994X
  251305. 1457Y
  251306. 59 (6)
  251307. Kanemasa, S.B
  251308. JACSC
  251309. Isoxazoline
  251310. Grignard Reagent
  251311. 21509N
  251312. 2/28/96
  251313. First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions.  High Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols W
  251314. 1994X
  251315. 2324Y
  251316. 116 (6)
  251317. Yamazaki, S.B
  251318. JACSCMSilicon Chemistry
  251319. Selenium Chemistry
  251320. Lewis Acid
  251321. Cyclopropane Synthesis
  251322. Enone
  251323. 21510N
  251324. 2/28/96Vg[2+1] Cycloaddition of Seleno-2-silylethenes.  Selenium Assisted 1,2-Silicon Shift for CyclopropanationW
  251325. 1994X
  251326. 2356Y
  251327. 116 (6)
  251328. Denmark, S. E.B
  251329. JACSC
  251330. Lithium CarbanionI
  251331. 21511N
  251332. 2/28/96V
  251333. Structure and Dynamics of Phosphorus (V) Stabilized Carbanions:  A Comparison of Theoretical, Crystallographic, and Solution StructuresW
  251334. 1994X
  251335. 2437Y
  251336. 116 (6)
  251337. Rawal, V. H.B
  251338. JACSCGReduction
  251339. Paterno Buchi Reaction
  251340. Diels-Alder
  251341. Radical Trapping Reaction
  251342. 21512N
  251343. 2/28/96
  251344. A General Strategy  for Increasing Molecular Complexity:  Photocycloaddition Fragmentation Route to Functionalized Di- and TriquinanesW
  251345. 1994X
  251346. 2613Y
  251347. 116 (6)
  251348. Paterson, I.B
  251349. JACSC0Allylsilane
  251350. Lewis Acid
  251351. Aldol Reaction
  251352. Reduction
  251353. 21513N
  251354. 2/28/96V$Total Syhthesis of (-)-Preswinolide
  251355. 1994X
  251356. 2615Y
  251357. 116 (6)
  251358. Hoye, T.B
  251359. JACSI
  251360. 21514N
  251361. 2/28/96V<A Total Synthesis of (+)-Xestospongin A/ (+)-Araguspongine DW
  251362. 1994X
  251363. 2617Y
  251364. 116 (6)
  251365. Rychnovsky, S. D.B
  251366. JACSCTAlkylation
  251367. Lithium Carbanion 
  251368. Cyanohydrin
  251369. Grignard Reagent for Conjugated Diene PrepI
  251370. 21515N
  251371. 2/28/96Vz1. Rapid Construction of the Roflamycoin System
  251372. 2. Stereochemical Assignment of Roflamycoin by C-13 NMR Acetonide AnalysisW
  251373. 1994X
  251374. 2621, 2623Y
  251375. 116 (6)
  251376. Meyers, A. I.B
  251377. JACSC%Alkylation
  251378. Lithium Enolate
  251379. ThiolactamI
  251380. 21516N
  251381. 2/28/96
  251382. Thio Claisen Rearrangements.  An Asymmetric Synthesis of 4,4-Disubstituted Cyclohexenones with Vicinal Quaterary and Tertiary StereocentresW
  251383. 1994X
  251384. 2633Y
  251385. 116 (6)
  251386. Kita, Y.B
  251387. JOC C
  251388. Lewis Acid
  251389. Nitrile Synthesis
  251390. 21517N
  251391. 2/28/96VhAn Unprecedented Cleavage of the b-Lactam ring :  Stereoselective Synthesis of Chiral b-Amido Cyanides 
  251392. 1994X
  251393. 59 (5)
  251394. Momose, T.B
  251395. JOCC2Cuprate Chemistry
  251396. Conjugate Addition
  251397. Organocopper
  251398. 21518N
  251399. 2/28/96V
  251400. Asymmetric Synthesis of the Indolizidine Alkaloids 207A, 209B, and 235B':  6-Substituted 2,3-Didehydropiperidine-2-carboxylate as a Versatile Chiral Building BlockW
  251401. 1994X
  251402. 59 (5)
  251403. Dittmer, D. C.B
  251404. JOCC0Super Hydride 
  251405. Boron Hydride Reduction
  251406. TelluriumI
  251407. K4-Te and super hydride produces telluride ion ( Te2-)M
  251408. 21519N
  251409. 2/28/96V_Concomitant Epoxide Deoxygenation and Deacylation of Glycidyl Acetates Induced by Telluride IonW
  251410. 1994X
  251411. 1004Y
  251412. 59 (5)
  251413. Feldman, K. S.B
  251414. Annulation
  251415. Organostannane
  251416. 21520N
  251417. 2/28/96V
  251418. Thoamide and Thioester Cyclopentane Synthesis via Trimethyltin Radical Catalyzed Alkenylation of Substituted (Thiocarbonyl)cyclopropanesW
  251419. 1994X
  251420. 1129Y
  251421. 59 (5)
  251422. Liebeskind, L. S.B
  251423. Rearrangement
  251424. 21521N
  251425. 2/28/96V
  251426. A Method for the Stereoselective Construction of 4-Alkoxy -5-Alkylidenecyclopentenones by the Tandem Ring Expansion-Functionalization of 1-Alkynylcyclobutenols Using a Palladium Mercury Cocatalytic SystemW
  251427. 1994X
  251428. 1149Y
  251429. 59 (5)
  251430. Mulzer, J.B
  251431. JOCCoIreland Claisen Rearrangement
  251432. Enantioselective Diethyl Zinc Addition
  251433. Clelate Cram Griganrd Addition
  251434. Osmylation
  251435. 21522N
  251436. 2/28/96VTStereoselective Synthesis of the Bis-tetrahyrrofuran fragment (C1-C-9) of AsteltoxinW
  251437. 1994X
  251438. 1160Y
  251439. 59 (5)
  251440. Guindon, Y.B
  251441. JOCCNTributyl Tin Hydride
  251442. Boron Lewis Acid Mediated Ring Opening
  251443. IodoetherificationI
  251444. 21523N
  251445. 2/28/96
  251446. Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals.  Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction:  Synthesis of the C17-C22 Subunit of Ionomycin  W
  251447. 1994X
  251448. 1166Y
  251449. 59 (5)
  251450. Charette, A. B.B
  251451. JACSC#Cyclopropane
  251452. Chiral Lewis Acid
  251453. ZincI
  251454. 21524N
  251455. 2/28/96VtDesign of Amphoteric Bifunctional Ligands to the Enantioselective Simmons-Smith Cyclopropanation of Allylic AlcoholsW
  251456. 1994X
  251457. 2651Y
  251458. 116 (6)
  251459. Paquette, L. A.B
  251460. JACSC7Palladium Stille Coupling
  251461. Enol Triflate
  251462. Organostannane
  251463. 21525N
  251464. 2/28/96V
  251465. Enantioselective Synthesis of Natural (-)-Austalide B, an Unusual Ortho Ester Metabolite Produced by Toxigenic Cultures of Aspergillus ustusW
  251466. 1994X
  251467. 2665Y
  251468. 116 (6)
  251469. Paquette, L. A.B
  251470. JACSC2Claisen Condensation
  251471. Potassium Enolate
  251472. Keto Ester
  251473. 21526N
  251474. 2/28/96V
  251475. Enantioselective Synthesis of Natural (-)-Austalide B, an Unusual Ortho Ester Metabolite Produced by Toxigenic Cultures of Aspergillus ustusW
  251476. 2665Y
  251477. 116 (6)
  251478. A    Padwa, A.B
  251479. JACSCfCyclopropane Synthesis
  251480. Rhodium Acetate
  251481. Samarium Iodide Deoxygenation
  251482. Reduction
  251483. Rhodium Carbene ComplexI
  251484. 21527N
  251485. 2/28/96V
  251486. Synthetic Studies toward Illudins and Ptaquilosin.  A Highly Convergent Approach via the Dipolar Cycloaddition of Carbonyl YlidesW
  251487. 1994X
  251488. 2667Y
  251489. 116 (6)
  251490. A    Ogawa, A.B
  251491. JOCC?Vinyl Tellurides
  251492. Cuprates
  251493. Lithium Tellurium Exchange
  251494. Carbanion
  251495. 21528N
  251496. 2/28/96VbHighly Regio- and Stereoselective Alkylation of vic-Bis(phenyltelluro)alkenes with Organocuprates W
  251497. 1994X
  251498. 1600Y
  251499. 59 (7)
  251500. A    Shono, T.B
  251501. JOCC"Annulation
  251502. Radical Anion
  251503. ReductionI
  251504. 21529N
  251505. 2/28/96V
  251506. Electroorganic Chemistry.  144.  Electroreductive Coupling of Ketones with O-Methyl Oximes, N,N-Dimethylhydrazones, and Nitrones.  A Convenient Route to Synthesis of b-Amino AlcoholW
  251507. 1994X
  251508. 1730Y
  251509. 59 (7)
  251510. Evans, D. A.B
  251511. JACSC4Aziridine
  251512. Silyl Enol Ether
  251513. a-Amino Ketone Synthesis
  251514. 21530N
  251515. 2/28/96
  251516. VBDevelopement of the Copper Catalyzed Olefin Aziridination ReactionW
  251517. 1994X
  251518. 2742Y
  251519. 116 (7)
  251520. Mikami, K.B
  251521. JACSCUChiral Organotitanium Catalyst
  251522. Hetero-Diels-Alder Reaction
  251523. Tetrahydropyran Synthesis
  251524. 21531N
  251525. 2/28/96V
  251526. Asymmetric Catalysis of Diels-Alder Cycloadditions by an MS-Free Binaphthol Titanium Complex:  Dramatic Effect of MS, Linear vs Positive Nonlinear Relationship, and Synthetic ApplicationsW
  251527. 1994X
  251528. 2812Y
  251529. 116 (7)
  251530. Smith, R. A. J.B
  251531. JACSI
  251532. 21532N
  251533. 2/28/96V
  251534. The Mechanism of Organocuprate 1,4-Addition Reactions with a,b-unsaturated Ketones:  Formation of Cuprate Enone Complexes with Lithium DimethylcuprateW
  251535. 1994X
  251536. 2902Y
  251537. 116 (7)
  251538. Wulff, W. D.B
  251539. JACSC]Chromium Carbonyl Complex
  251540. Organostannane
  251541. Annulation
  251542. Phenol Synthesis
  251543. Fischer Carbene Complex
  251544. 21533N
  251545. 2/28/96V\Contrasteric Regiochemical Incorporation of Stannylacetylenes in the Benzannulation ReactionW
  251546. 1994X
  251547. 3113Y
  251548. 116 (7)
  251549. Hoveyda, A. H.B
  251550. CdGrignard Reagent
  251551. Zirconium
  251552. Ruthenium Complex
  251553. Asymmetric Catalytic Carbomagnesation
  251554. Olefin MetathesisI
  251555. 21534N
  251556. 2/28/96V0Zirconium Catalyzed Kinetic Resolution of PyransW
  251557. 1994X
  251558. 3123Y
  251559. 116 (7)
  251560. Fukuyama, T.B
  251561. JACSC
  251562. Copper (II) Catalyzed Cyclopropane Prep
  251563. Bromination of Lithium Enolate
  251564. Intramolecular Cyclopropanation
  251565. Aldol Reaction
  251566. Cationic Cyclization
  251567. Annulation
  251568. Palladium Carbonylation
  251569. Indole Synthesis
  251570. Michael Addition of LiCH(SMe)(SOMe)
  251571. Curtius Reaction
  251572. 21535N
  251573. 2/28/96V/Stereocontrolled Synthesis of (-)-Hapalindole GW
  251574. 1994X
  251575. 3125Y
  251576. 116 (7)
  251577. Fukuyama, T.B
  251578. JACSC
  251579. Radical Ring Closure
  251580. Organostannane
  251581. Isonitrile
  251582. Palladium Stille Coupling
  251583. 2,3-Disubstituted Indole Synthesis
  251584. Imidoyl Radical
  251585. ORTHO ALKENYL ARYL ISONITRILE, TIN HYDRIDE, ALPHA STANNYLIMIDOYL RADICAL, IMIDOYL, CYCLIZATION TO INDOLE, STILLE COUPLINGI
  251586. 21536N
  251587. 2/28/96V%A Novel Tin Mediated Indole SynthesisW
  251588. 1994X
  251589. 3127Y
  251590. 116 (7)
  251591. Curran, D. P.B
  251592. CLRadical 
  251593. Cycloaddition
  251594. Organostannane
  251595. Chiral Auxillary
  251596. Diels-Alder Reaction
  251597. High Barrier to Bond RotationM
  251598. 21537N
  251599. 2/28/96VFAtroposelective Thermal Reactions of Axially Twisted Amides and ImidesW
  251600. 1994X
  251601. 3131Y
  251602. 116 (7)
  251603. Oppolzer, W.B
  251604. JACSCSRetro Cope Elimination Mechanism
  251605. Pictet Spengler Cyclization
  251606. Cuprate SN2' Reaction
  251607. K<Reaction proceeds stereospecifically in a suprafacial mannerM
  251608. 21538N
  251609. 2/28/96VpSuprafaciality of Thermal N-4-Alkenylhydroxylamine Cyclizations:  Synthesis of (
  251610. )-a-Lycorane and (+)-TrianthineW
  251611. 1994X
  251612. 3139Y
  251613. 116 (7)
  251614. Corey, E. J.B
  251615. JACSI
  251616. 21539N
  251617. 2/28/96V\Chemical Emulation of the Biosynthetic Route to Glycinoelepin from a Cycloartenol DerivativeW
  251618. 1994X
  251619. 3149Y
  251620. 116 (7)
  251621. Corey, E. J.B
  251622. JACSCLOrganostannane
  251623. Boron Chiral Promoter
  251624. Asymmetric Propargyl Alcohol Synthesis
  251625. 21540N
  251626. 2/28/96VUHighly Enantioselective Alkynylation of Aldehydes Promoted by Chiral OxazaborolidinesW
  251627. 1994X
  251628. 3151Y
  251629. 116 (7)
  251630. A    Jeong, N.B
  251631. JACSC4Cobalt Mediated Annulation
  251632. Cyclopentenone Synthesis
  251633. 21541N
  251634. 2/28/96V.Catayltic Version of the Pauson Khand ReactionW
  251635. 1994X
  251636. 3159Y
  251637. 116 (7)
  251638. Yamamoto, Y.B
  251639. JACSCOAmino ester Synthesis
  251640. Amino nitrile Synthesis
  251641. Rhodium Transition Metal CatalystI
  251642. 21542N
  251643. 2/28/96VETransition Metal Catalyzed Addition of Certain Nucleophiles to IminesW
  251644. 1994X
  251645. 3161Y
  251646. 116 (7)
  251647. Trost, B. M.B
  251648. JACSCbMichael Addition
  251649. Acetylene
  251650. a,b-Unsaturated Carbonyl Compound
  251651. Vinyl Triphenylphosphine IntermediateI
  251652. KP Nucleophilic g Addition to Acetylenes Bearing Electron Withdrawing SubstituentsM
  251653. 21543N
  251654. 2/28/96VGNovel "Umpolung" in C-C Bond Formation Catalyzed by Triphenyl PhosphineW
  251655. 1994X
  251656. 3167Y
  251657. 116 (7)
  251658. A    Kahne, D.B
  251659. JACSC?Enediyne Antibiotics
  251660. DNA Cleavage
  251661. Diradical
  251662. Bergman CyclizationI
  251663. 21544N
  251664. 2/28/96VeAnalysis of Hydroxylamine Glycoside Linkages:  Structural Consequenes of the NO Bond in CalicheamicinW
  251665. 1994X
  251666. 3197Y
  251667. 116 (8)
  251668. Beak, P.B
  251669. JACSC9Lithium Carbanion
  251670. Sparteine
  251671. trans-2,5-dimethylpyrrolidineI
  251672. 21545N
  251673. 2/28/96VwComplex Induced Proximity Effects:  Enantioselective Syntheses Based on Asymmetric Deprotonations of N-Boc-pyrrolidinesW
  251674. 1994X
  251675. 3231Y
  251676. 116 (8)
  251677. A    Adams, J.B
  251678. JACSC,Rhodium Carbene
  251679. Diazoketone
  251680. Rhodium Acetate
  251681. 21546N
  251682. 2/28/96VaModel Studies of the Stereoelectronic Effect in Rh(II) Mediated Carbenoid C-H Insertion ReactionsW
  251683. 1994X
  251684. 3296Y
  251685. 116 (8)
  251686. Paquette, L. A.B
  251687. JACSC Horner Emmons Wadsworth ReactionI
  251688. 21547N
  251689. 2/28/96V
  251690. Total Synthesis of the Cembranoid Diterpene Lactone (+)-Clemeolide.  Some Remarkable Conformational Features of Nine-Membered Belts Linked in 2,6-Fashion to a MethylenecyclohexaneW
  251691. 1994X
  251692. 3367Y
  251693. 116 (8)
  251694. Corey, E. J.B
  251695. JACSC1Boron Lewis Acid Catalyst
  251696. Tryptophan
  251697. Amino Acid 
  251698. 21548N
  251699. 2/28/96
  251700. Demonstration of the Synthetic Power of Oxazaborolidine Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberlic AcidW
  251701. 1994X
  251702. 3612Y
  251703. 116 (8)
  251704. Paterson, I.B
  251705. JACSC
  251706. Boron Enolate
  251707. Tin Enolate
  251708. 21549N
  251709. 2/28/96VrSubstrate Controlled Aldol Reaction of Chiral Ethyl Ketones:  Application oto the Total Synthesis of Oleandomycin W
  251710. 1994X
  251711. 3623Y
  251712. 116 (8)
  251713. A    Ojima, I.B
  251714. JACSC6Rhodium Catalyzed Carcosilation of Alkynes
  251715. Annulation
  251716. 21550N
  251717. 2/28/96VNExtremly Chemoselective Silylformylation and Silylcarbocyclization of AlkynalsW
  251718. 1994X
  251719. 3643Y
  251720. 116 (8)
  251721. Kita, Y.B
  251722. JACSC(Cation Radical Mechanism
  251723. Oxidation
  251724. AzideI
  251725. 56% yieldM
  251726. 21551N
  251727. 2/28/96V
  251728. Hypervalent Iodine Induced Nucleophilic Substitution of para-Substituted Phenol Ethers.  Generation of Cation Radicals as Reactive IntermediatesW
  251729. 1994X
  251730. 3684Y
  251731. 116 (9)
  251732. Nicolaou, K. C.B
  251733. C>Enedyne Antibiotics
  251734. DNA Cleavage
  251735. Diradical
  251736. Bergman CyclizationI
  251737. 21552N
  251738. 2/28/96V~Interaction of Calicheamicin with Duplex DNA:  Role of the Oligosaccharide Domain and Identification of Multiple Binding ModesW
  251739. 1994X
  251740. 3697Y
  251741. 116 (9)
  251742. Nicolaou, K. C.B
  251743. JACSC>Enedyne Antibiotics
  251744. DNA Cleavage
  251745. Diradical
  251746. Bergman CyclizationI
  251747. 21553N
  251748. 2/28/96VXCarbohydrate-Minor Groove Interactions in the Binding of Calicheamycin g1I to Duplex DNAW
  251749. 1994X
  251750. 3709Y
  251751. 116 (9)
  251752. A    Togni, A.B
  251753. JACSC'Chiral Ligand for Asymmetric Catalysis
  251754. KZ2. An Unusual, Selective h3-h1 Allyl Isomerization in a Chiral Allylic Alkylation CatalystM
  251755. 21554N
  251756. 2/28/96V
  251757. 1. A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration ReactionsW
  251758. 1994X
  251759. 4062, 4067Y
  251760. 116 (9)
  251761. Mikami, K.B
  251762. JACSC
  251763.  BINOL Titanium Lewis AcidI
  251764. 21555N
  251765. 2/28/96
  251766. VxAsymmetric Catalytic Aldol Type Reaction with Silyl Ketene Acetals:  Possible Intervention of the Silatropic Ene PathwayW
  251767. 1994X
  251768. 4077Y
  251769. 116 (9)
  251770. Hatakeyama, S.B
  251771. JACSC
  251772. Photochemistry
  251773. [2+2] photocycloaddition
  251774. Vinyl Carbanion
  251775. Allenylmethyl trimethylsilane
  251776. Phenyliodine(III)diacetate Radical OxidationI
  251777. 21556N
  251778. 2/28/96V#Total Synthesis of (-)-PaeoniflorinW
  251779. 1994X
  251780. 4081Y
  251781. 116 (9)
  251782. Kobayashi, S.B
  251783. JACSC
  251784. Ytterbium Chiral Lewis AcidI
  251785. 21557N
  251786. 2/28/96V
  251787. Lanthanide(III)-Catalyzed Enantioselective Diels-Alder Reactions.  Stereoselective Synthesis of Both Enantiomers by Using a Single Chiral Source and a Choice of Achiral Ligands W
  251788. 1994X
  251789. 4083Y
  251790. 116 (9)
  251791. Trost, B. M.B
  251792. JACSC'Palladium Catalyst Mediated Alkylation
  251793. 21558N
  251794. 2/28/96VFAsymmetric Induction in Allylic Alkylations of 3-(Acyloxy)cycloalkenesW
  251795. 1994X
  251796. 4089Y
  251797. 116 (9)
  251798. RajanBabu, T. V.B
  251799. JACSC-Asymmetric Hydrogenation
  251800. Carbohydrate LigandsI
  251801. 21559N
  251802. 2/28/96
  251803. Electronic Amplification of Selectivity in Rhodium Catalyzed Hydrogenation:  D-Glucose Derived Ligands for the Synthesis of D- or L-Amino Acids W
  251804. 1994X
  251805. 4101Y
  251806. 116 (9)
  251807. Yamamoto, H.B
  251808. JACSCMLewis Acid 
  251809. Michael Addition
  251810. Oganolithium
  251811. Organomagnesium
  251812. Silyl Ketene AcetalI
  251813. Conjugate Addition favoured over 1,2-addition due to shielding of the aldehyde carbonyl being located in a tight pocket of the ATPH complex M
  251814. 21560N
  251815. 2/28/96V{Virtually Complete Blocking of a,b-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide)W
  251816. 1994X
  251817. 4131Y
  251818. 116 (9)
  251819. Winkler, J. D.B
  251820. JACSC#Photochemistry
  251821. Retro Aldol ReactionI
  251822. 21561N
  251823. 2/28/96V
  251824. Inside-Outside Stereisomerization . 6.  Synthesis of trans-Bicyclo[4.4.1]undecan-11-one and the First Stereoselective Construction of the Tricyclic Nucleus of the Ring System of the Ingenane DiterpenesW
  251825. 1994X
  251826. 4183Y
  251827. 116 (10)
  251828. Hayashi, T. B
  251829. C9Palladium Asymmetric Silylation
  251830. Chiral Ruthenium CatalystI
  251831. 21562N
  251832. 2/28/96VxOptically Active Ruthenocenylbis(phosphines):  New Effieient Chiral Phosphine Ligands for Catalytic Asymmetric ReactionsW
  251833. 1994X
  251834. 4221Y
  251835. 116 (10)
  251836. Trost, B. M.B
  251837. JACSC
  251838. Diels-Alder
  251839. Diene SynthesisI
  251840. 21563N
  251841. 2/28/96VFPalladium Catalyzed Cycloisomerization to 1,2-DialkylidenecycloalkanesW
  251842. 1994X
  251843. 4255, 4268Y
  251844. 116 (10)
  251845. Curran, D. P.B
  251846. JACSC3Selenium Chemistry 
  251847. Atom Transfer Radical ChemistryI
  251848. 21564N
  251849. 2/28/96VFGroup Transfer Addition Reactions of Methyl(phenylseleno)malononitrileW
  251850. 1994X
  251851. 4279Y
  251852. 116 (10)
  251853. Dussault, P. H.B
  251854. JACSC*Radical Addition
  251855. Organostannane
  251856. Oxidation
  251857. 21565N
  251858. 2/28/96VmStereoselective Dioxygenation of Allylstannanes:  Synthesis of Enantiomerically Enriched Allyl HydroperoxidesW
  251859. 1994X
  251860. 4485Y
  251861. 116 (10)
  251862. Martin, S. F.B
  251863. JACSC
  251864. Rhodium Carbene Complex
  251865. 21566N
  251866. 2/28/96
  251867. VkEnantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic DiazoacetatesW
  251868. 1994X
  251869. 4493Y
  251870. 116 (10)
  251871. Magnus, P.B
  251872. JACSC%Azide Synthesis
  251873. Oxidation
  251874. Lewis Acid
  251875. 21567N
  251876. 2/28/96V
  251877. a-Azidonation of Amides, Carbamates, and Ureas with the Iodosylbenzene/ Trimethylsilyl Azide Reagent Combination: N-Acyliminium Ion PrecursorsW
  251878. 1994X
  251879. 4501Y
  251880. 116 (10)
  251881. Doyle, M. P.B
  251882. JACSCeRhodium Carbebe Complex
  251883. Diazoester
  251884. Chiral Dirhodium (II) Carboxamide Catalyst
  251885. C-H Insertion Reaction
  251886. 21568N
  251887. 2/28/96VlDiastereocontrol for Highly Enantioselective Carbon-Hydrogen Insertion Reactions of Cycloalkyl DiazoacetatesW
  251888. 1994X
  251889. 4507Y
  251890. 116 (10)
  251891. Johnson, C. R. B
  251892. Silyl Enol Ether
  251893. Reduction
  251894. 21569N
  251895. 2/28/96V
  251896. Hydrosilylation of Enones:  Platinum Divinyltetramethyldisiloxane Complex in the Preparation of Triisopropylsilyl and Triphenylsilyl Enol EthersW
  251897. 1994X
  251898. 2287Y
  251899. 59 (9)
  251900. Brown, H. C.B
  251901. Aldol Chemistry
  251902. Boron EnolateI
  251903. 21570N
  251904. 2/28/96V
  251905. Enolboration. 6.  Dicyclohexyliodoborane, a Versitile Reagent for the Stereoselective Synthesis of Either Z or E Enolates from Representative Esters W
  251906. 1994X
  251907. 2336Y
  251908. 59 (9)
  251909. Brown, H. C.B
  251910. 21571N
  251911. 2/28/96
  251912. SHydroboration.  91.  Improved Procedure for the Synthesis of Optically Pure Bis-Adducts, N,N,N',N'-Tetramethyletylenediamine
  251913. 2-organylapiosopinocampheylboranes, from the Corresponding 2-Organylapopinenes of Lower Optical Purity.  Conversion of These Adducts into 2-Organylapoisopinocampheylboranes, Useful Asymmetric Hydroboraing Reagents 
  251914. 1994X
  251915. 2365Y
  251916. 59 (9)
  251917. Meyers, A. I.B
  251918. JOCCLAsymmetric Ullmann Coupling
  251919. Chiral Biaryl Synthesis
  251920. Copper Mediated CouplingI
  251921. 21572N
  251922. 2/28/96V*A Rapid Total Synthesis of an EllagitanninW
  251923. 1994X
  251924. 2577, 2655Y
  251925. 59 (9)
  251926. ISHIKURA, M.
  251927. JOCCDPalladium Coupling
  251928. Boron Ate Complex
  251929. Indole Synthesis
  251930. Carbonylation
  251931. 21573N
  251932. 2/28/96
  251933. Palladium Catalyzed Carbonylative Cross Coupling Reactions with Triethyl(1-methylindol-2-yl)borate:  A Simple Route to 1-Methylindol-2-yl KetonesW
  251934. 1994X
  251935. 2634Y
  251936. 59 (9)
  251937. Rychnovsky, S. D.B
  251938. Acetylene to AlkeneI
  251939. 21574N
  251940. 2/28/96V`Triphenylphosphine Catalyzed Isomerizations of Enynes to (E,E,E) tienes:  Phenol as a CocatalystW
  251941. 1994X
  251942. 2659Y
  251943. 59 (9)
  251944. Shibasaki, M.B
  251945. JOCC,Nitroaldol
  251946. Cyanosilylation
  251947. Lanthanide Bases
  251948. 21575N
  251949. 2/28/96V
  251950. Catalytic Aldol Reactions with Sm(HMDS)3 and its Application for the Introduction of a Carbon-Carbon Triple Bond at C-13 in Prostaglandin SynthesisW
  251951. 1994X
  251952. 2661Y
  251953. 59 (9)
  251954. Martin, S. F.B
  251955. JACSC
  251956. Asymmetric Aldol Reaction
  251957. Oxidation of Furan Ring
  251958. Stereoselective Cuprate Addition
  251959. Lewis Acid Addition of Crotyl Stannane
  251960. Stereoselective Reduction of KetoneI
  251961. 21576N
  251962. 2/28/96VhStategies for Macrolide Synthesis.  A Concise Approach to Protected Seco-Acids of Erythronolides A and BW
  251963. 1994X
  251964. 4674Y
  251965. 116 (11)
  251966. Paquette, L. A. B
  251967. JACSC}Double Michael Addition Ring Annulation
  251968. Conjugate Addition
  251969. Lithio(TMS)acetonitrile
  251970. Radical Deoxygenation of a SelenocarbonateI
  251971. 21577N
  251972. 2/28/96VuTotal Synthesis of the Lycopodium Alkaloids Magellanine and Magellaninone by Threefold Annulation of 2-CyclopentenoneW
  251973. 1994X
  251974. 4689Y
  251975. 116 (11)
  251976. Meyers, A. G. B
  251977. JACSCXTriethyl Boron Initiated Radical Cyclization
  251978. Carbohydrate Chemistry
  251979. Glycoside Coupling
  251980. 21578N
  251981. 2/28/96V
  251982. Synthetic Studies on the Tunicamycin Antibiotics.  Preparation of (+)-Tunicaminyluracil, (+)-Tunicamycin-V, and 5'-epi-Tunicamycin-VW
  251983. 1994X
  251984. 4697Y
  251985. 116 (11)
  251986. Comins, D. L.B
  251987. JACSC)Chiral Pyridinium Salts
  251988. Dihydropyridones
  251989. 21579N
  251990. 2/28/96V
  251991. Asymmetric Synthesis of 2-Alkyl(Aryl)-2,3-dihydro-4-pyridones by Addition of Grignard Reagents to Chiral 1-Acyl-4-methoxypyridinium SaltsW
  251992. 1994X
  251993. 4719Y
  251994. 116 (11)
  251995. Frenking, G.B
  251996. C]Asymmetric Osmylation
  251997. Osmium Tetroxide
  251998. Diol Synthesis
  251999. Oxidation of Alkenes
  252000. Cinchona AlkaloidsI
  252001. 21580N
  252002. 2/28/96VcMechanism of the Enantioselective Dihyroxylation of Olefins by OsO4 in the Presence of Chiral BasesW
  252003. 1994X
  252004. 4937Y
  252005. 116 (11)
  252006. Jimenez, L. S.B
  252007. JACSCGDNA Alkylation
  252008. Annulation
  252009. Michael Addition
  252010. Epoxide Synthesis
  252011. Aziridine
  252012. 21581N
  252013. 2/28/96VQSynthesis of the Tetracyclic Mitomycin Skeleton via a Dialkylvinyl Sulfonium SaltW
  252014. 1994X
  252015. 4977Y
  252016. 116 (11)
  252017. Majetich, G.B
  252018. JACSCELewis Acid Catalyzed Cycloalkylation
  252019. Carbocation Mediated Annulation
  252020. 21582N
  252021. 2/28/96V#Concise Synthesis of (
  252022. )-PerovskoneW
  252023. 1994X
  252024. 4979Y
  252025. 116 (11)
  252026. Majetich, G.B
  252027. JACSC3Europium Catalyzed Diels-Alder Reaction
  252028. Lewis Acid
  252029. 21583N
  252030. 2/28/96V#Concise Synthesis of (
  252031. )-PerovskoneW
  252032. 1994X
  252033. 4979Y
  252034. 116 (11)
  252035. Trost, B. M.B
  252036. JACSC@Terminal Olefins
  252037. Acetylene
  252038. Transition Metal Mediated Annulation
  252039. Terminal olefins only
  252040. 21584N
  252041. 2/28/96
  252042. Buteneolide Synthesis Based Upon a Contra-Electronic Addition in a Ruthenium Catalyzed Alder Ene Reaction.  Synthesis and Absolute Configuration of (+)-AncepsenolideW
  252043. 1994X
  252044. 4985Y
  252045. 116 (11)
  252046. A    Kishi, Y.B
  252047. JACSI
  252048. 21585N
  252049. 2/28/96V5Novel Structure Elucidation of AAL Toxin TA Backbone
  252050. 1994X
  252051. 4995Y
  252052. 116 (11)
  252053. Boger, D. L.B
  252054. JACSI
  252055. 21586N
  252056. 2/28/96V
  252057. Total Synthesis of Bleomycin and Related Agents.  1. Synthesis and DNA Binding Properties of the Extended C-Terminus:  Tripeptide S, Tetrapeptide S, Pentapeptide S, and Related AgentsW
  252058. 1994X
  252059. 5607, 5619, 5631, Y
  252060. 116 (13)
  252061. Hartwig, J. F.B
  252062. JACSC!Organostannane
  252063. Aniline Synthesis
  252064. 21587N
  252065. 2/28/96V
  252066. Palladium Catalyzed Formation of Carbon-Nitrogen Bonds.  Reaction Intermediates and Catalyst Improvements in the Hetero Cross-Coulping of Aryl Halides and Tin AmidesW
  252067. 1994X
  252068. 5969Y
  252069. 116 (13)
  252070. Buchwald, S. F.B
  252071. JACSC;Optically Active Amine
  252072. Chiral Titanium Catalyst
  252073. Reduction
  252074. 21588N
  252075. 2/28/96VFAsymmetric Hydrogenation of Enamines with a Chiral Titanocene CatalystW
  252076. 1994X
  252077. 5985Y
  252078. 116 (13)
  252079. Fuchs, P. L.B
  252080. JACSC
  252081. Sulfone Carbanion
  252082. 21589N
  252083. 2/28/96V
  252084. A Highly Efficient Synthesis of b-Substituted Six- and Seven -Membered-Ring Enones via Carbon Alkylation of g-Methoxy  Allylsulfonyl AnionsW
  252085. 1994X
  252086. 5995Y
  252087. 116 (13)
  252088. Collum, D. B.B
  252089. JACSC
  252090. Li nmr
  252091. Carbanion
  252092. 21590N
  252093. 2/28/96VpStructure of Lithium Hexamethyldisilazide:  Spectroscopic Study of Ethereal Solvation in the Slow Exchange LimitW
  252094. 1994X
  252095. 6009Y
  252096. 116 (13)
  252097. Yamamoto, Y.B
  252098. JACSI
  252099. 21591N
  252100. 2/28/96VTPalladium Catalyzed Addition of Activated Methylene and Methyne Compounds to AllenesW
  252101. 1994X
  252102. 6019Y
  252103. 116 (13)
  252104. A    Murai, S.B
  252105. JACSCBAnnulation
  252106. Ruthenium Complex Catalyzed Cyclization
  252107. Diene SynthesisI
  252108. 21592N
  252109. 2/28/96VsHighly Selective Skeletal Reorganization of 1,6- and 1,7-Enynes to 1-Vinyl Cycloalkenes Catalyzed by  [RuCl2(CO)3]2W
  252110. 1994X
  252111. 116 (13)
  252112. Yamamoto, H.B
  252113. JACSC?Conjugate Addition
  252114. Carboxylation
  252115. Addition to Aldehyde or KetoneI
  252116. 21593N
  252117. 2/28/96VjAllylbarium Reagents:  Unprecedented Regio- and Stereoselective Allylation Reactions of Carbonyl CompoundsW
  252118. 1994X
  252119. 6130Y
  252120. 116 (14)
  252121. Yamamoto, H.B
  252122. JACSC
  252123. Lewis Acid
  252124. 21594N
  252125. 2/28/96V
  252126. Asymmetric Diels-Alder Reaction of Unsymetrical Maleates.  A Chemical Access to Chiral, Unsymetrical cis-Cyclohexene-1,2-dicarboxylatesW
  252127. 1994X
  252128. 6153Y
  252129. 116 (14)
  252130. Stille, J. R.B
  252131. JACSC+Annulation
  252132. Enamine
  252133. Imine
  252134. Michael Addition 
  252135. 21595N
  252136. 2/28/96VvAsymmetric Formation of Quaternary Centres through Aza-Annulation of Chiral b-Enamino Esters with Acrylate DerivativesW
  252137. 1994X
  252138. 6201Y
  252139. 116 (14)
  252140. Meyers, A. I.B
  252141. JACSC#Chiral Oxazoline
  252142. Conjugate AdditionI
  252143. 21596N
  252144. 2/28/96VeAsymmetric Michael Type Addition of Lithium Amides to Aromatic Systems Leading to Novel b-Amino acidsW
  252145. 1994X
  252146. 6437Y
  252147. 116 (14)
  252148. Wulff, W. D.
  252149. JACSC.Annulation
  252150. Phenol Synthesis
  252151. CycloaromatizationI
  252152. 21597N
  252153. 2/28/96V[First Stereoselective Synthesis of Arene Chromium Complexes via the Benzannulation ReactionW
  252154. 1994X
  252155. 6449Y
  252156. 116 (14)
  252157. Nishida, M.B
  252158. JACSC4Radical Cyclization
  252159. Organnostannane
  252160. Chiral AuxiliaryI
  252161. 21598N
  252162. 2/28/96V^Lewis Acid Promoted Diastereoselective Radical Cyclization Using Chiral a,b-unsaturated EstersW
  252163. 1994X
  252164. 6455Y
  252165. 116 (14)
  252166. Roush, W. R.B
  252167. JACSC
  252168. Intramolecular Diels-Alder
  252169. Asymmetric Borane Reduction
  252170. Palladium Suzuki Coupling
  252171. Horner Emmons Olefination
  252172. BOP-Cl promoted Macrolactonization
  252173. LiHMDS Dieckmann CyclizationI
  252174. 21599N
  252175. 2/28/96V9Enantioselective Total Synthesis of  (-)-ChlorothricolideW
  252176. 1994X
  252177. 6457Y
  252178. 116 (14)
  252179. Boger, D. L.B
  252180. JACSC%DNA Alkylation
  252181. Antitumor Antibiotics
  252182. 21600N
  252183. 2/28/96
  252184. Chemical and Structural Comparison of N-BOC-CBQ and N-BOC-CBI:  Identification and Structural Orgin of an Unappreciated but Productive Stability of the CC-1065 and Duocarmycin SA Alkylation SubunitsW
  252185. 1994X
  252186. 6461Y
  252187. 166 (14)
  252188. Schreiber, S. L.B
  252189. SynlettC
  252190. FK506
  252191. RapamycinI
  252192. 21601N
  252193. 2/28/96V;Synthesis, Structure and Mechanism in Immunophilin ResearchW
  252194. 1994X
  252195. no. 6
  252196. Burgess, K.B
  252197. JACSC)Transition Metal Catalyzed Hydroboration
  252198. 21602N
  252199. 2/28/96V5Titanium Mediated Additions of Borohydride to AlkenesW
  252200. 1994X
  252201. 6561Y
  252202. 116 (15)
  252203. Jacobsen, E. J.B
  252204. JACSC+Manganese Salen Complex
  252205. Cinchonda AlkaloidsI
  252206. 21603N
  252207. 2/28/96V
  252208. Effect of Chiral Quaternary Ammonium Salts on (salen)-Mn-Catalyzed Epoxidation of cis-Olefins.   A Highly Enantioselective, Catalytic Route to Trans EpoxidesW
  252209. 1994X
  252210. 6937Y
  252211. 116 (15)
  252212. Hart, D. J.B
  252213. JACSC?Radical Cyclization
  252214. Reduction Triethylsilane
  252215. Tebbe Olefination
  252216. 21604N
  252217. 2/28/96
  252218. V%Total Synthesis of dl-21-OxogelsemineW
  252219. 1994X
  252220. 6943Y
  252221. 116 (15)
  252222. Barluenga, J. B
  252223. JACSC%Chromium Complex
  252224. Chiral D-A Reaction
  252225. 21605N
  252226. 2/28/96V
  252227. Asymmetric Exo-Selective Diels-Alder Reaction of Cyclic BF2 Adducts of Functionalized Fischer Vinylcarbene Complexes with Chiral 2-Amino-1,3-dienes W
  252228. 1994X
  252229. 6949Y
  252230. 116 (15)
  252231. Kahne, D. B
  252232. JACSC;Glycoside
  252233. Solid Phase Carbohydrate Synthesis
  252234. OligosaccarideI
  252235. 21606N
  252236. 2/28/96V?Glycosylation on the Merrifield Resin Using Anomeric SulfoxidesW
  252237. 1994X
  252238. 6953Y
  252239. 116 (15)
  252240. Canary, J. W.B
  252241. JACSC-Palladium Catalyzed Coupling of Bornic Acids
  252242. 21607N
  252243. 2/28/96V_Observation of Catalytic Intermediates in the Suzuki Reaction by Electrospray Mass SpectrometryW
  252244. 1994X
  252245. 6985Y
  252246. 116 (15)
  252247. Denmark, S. E.B
  252248. JACSCSLewis Acid Catalyzed Aldol Reaction
  252249. Mukaiyama Aldol
  252250. Silicon
  252251. Hydroxy Ester SynthesisI
  252252. 21608N
  252253. 2/28/96VQChemistry of Enoxysilacyclobutanes:  Highly Selective Uncatalyzed Aldol AdditionsW
  252254. 7026Y
  252255. 116 (16)
  252256. Semmelhack, M. F.
  252257. Wulff, W. D.B
  252258. JACSC
  252259. Mo Complexes
  252260. Annulation
  252261. 21609N
  252262. 2/28/96V
  252263. Metal Catalyzed Cyclopropene Rearrangements for Benzoannulation:  Evaluation of an Anthraquinone Synthesis Pathway and Reevaluation of the Parallel Approach via Carbene Chromium ComplexesW
  252264. 1994X
  252265. 7108Y
  252266. 116 (16)
  252267. Yamada, K.B
  252268. JACSC
  252269. Evans Syn Aldol Reaction
  252270. Sharpless Epoxidation
  252271. Horner-Emmons
  252272. Julia Coupling
  252273. Macrolactonization (Yamaguchi method)
  252274. Sulfone Li Carbanion 
  252275. AlkylationI
  252276. 21610N
  252277. 2/28/96V
  252278. 1. Absolute Stereochemistry of Aplyronine A, a Potent Antitumor Substance of Marine Orgin 
  252279. 2. Total Synthesis of Aplyronine A, a Potent Antitumor Substance of Marine Orgin W
  252280. 1994X    7441,7443Y
  252281. 116 (16)
  252282. Fallis, A. G.B
  252283. JACSC
  252284. Annulation
  252285. K*Also see A. Fallis JOC 1994, 59 (22), 6514M
  252286. 21611N
  252287. 2/28/96VOSamarium(II) Iodide Induced Radical Cyclization of Halo- and CarbonylhydrazonesW
  252288. 1994X
  252289. 7447Y
  252290. 116 (16)
  252291. Wulff, W. D.B
  252292. C,Organnostannane
  252293. Annulation
  252294. Chromium Complex
  252295. 21612N
  252296. 2/28/96VSPalladium Catalyzed Cross Coupling of Arene-Chromium Tricarbonyl Triflate ComplexesW
  252297. 1994X
  252298. 7449Y
  252299. 116 (16)
  252300. Semmelhack, M. F.B
  252301. JACSC
  252302. Palladium Catalyzed Cyclization
  252303. Palladium Hydrostannylation
  252304. Claisen Rearrangement
  252305. Radical Deoxygenation
  252306. Corey Oxazaborolidine Chiral ReductionI
  252307. 21613N
  252308. 2/28/96V
  252309. Palladium Promoted Synthesis of Ionophore Antibiotics.  Strategy and Assembly of the Homochiral Tetrahydrofuran and Tetrahydropyran Portions of TetronomycinW
  252310. 1994X
  252311. 7455Y
  252312. 116 (16)
  252313. Trost, B. M.B
  252314. JACSCDRamberg Blacklund Reaction
  252315. Ruthenium Catalyzed Butenolide AnnulationI
  252316. 21614N
  252317. 2/28/96VIA Concise Convergent Synthesis to Acetogenins.  (+)-Solamin and AnologuesW
  252318. 1994X
  252319. 7459Y
  252320. 116 (16)
  252321. A    Knapp, S.B
  252322. JACSC7Thiourea
  252323. Mercuric Oxide Mediated Cyclization
  252324.  OxazolineI
  252325. 21615N
  252326. 2/28/96VEA (1 - 4) "Trehazoloid Glucosidase Inhibitor with Aglycon SelectivityW
  252327. 1994X
  252328. 7461Y
  252329. 116 (16)
  252330. Grieco, P. A.B
  252331. JACSC8Copper (II) Mediated Ring Contraction
  252332. Lactone Synthesis
  252333. 21616N
  252334. 2/28/96V3C19 Quassinoids:  Total Synthesis of dl-Samaderin BW
  252335. 1994X
  252336. 7606Y
  252337. 116 (17)
  252338. Wulff, W. D.B
  252339. JACSC$Tungsten Carbene Cpmlex
  252340. Diels-Alder
  252341. 21617N
  252342. 2/28/96VyThree Component Intramolecular Two Alkyne Annulations of Fischer Carbene Complexes:  New Strategies for Steroid SynthesisW
  252343. 1994X
  252344. 7616Y
  252345. 116 (17)
  252346. Buchwald, S. L.B
  252347. JACSC
  252348. Organotin
  252349. Anilines
  252350. Arylamine
  252351. LiCl deactivates the reaction (product formed in the synthesis of the aminostannane).  The aminostannane was formed by reaction of N,N-diethylaminotributylstannane and the appropriate aniline with removal of the diethylamine.M
  252352. 21618N
  252353. 2/28/96VMPalladium Catalyzed Aromatic Aminations with in Situ Generated AminostannanesW
  252354. 1994X
  252355. 7901Y
  252356. 116 (17)
  252357. Sammakia, T.B
  252358. JACSC
  252359. Organotin 
  252360. Silyl Enol EtherI
  252361. 21619N
  252362. 2/28/96
  252363. VaEvidence for an Oxocarbenium Ion Intermediate in Lewis Acid Mediated Reactions of Acyclic AcetalsW
  252364. 1994X
  252365. 7915Y
  252366. 116 (17)
  252367. Takahashi, T.B
  252368. JACSC/Carbohydrate
  252369. Gylcoside Synthesis
  252370. OligosaccarideI
  252371. 21620N
  252372. 2/28/96VWSynthesis of An Elicitor-Active Analogue by a One-Pot, Two Step Glycosidation ProcedureW
  252373. 1994X
  252374. 7919Y
  252375. 116 (17)
  252376. Negishi, E-I.B
  252377. JACSC@Heck Cyclization
  252378. Annulation
  252379. Acylpalladium
  252380. Vinyl Iodide
  252381. palladiumI
  252382. 21621N
  252383. 2/28/96VnDeferred Carbonylative Esterification in the Palladium Catalyzed Cyclic Carbometallation-Carbonylation CascadeW
  252384. 1994X
  252385. 7923Y
  252386. 116 (17)
  252387. Collum, D. B.B
  252388. JACSC*Organolithium
  252389. Aggregation of Lithium AmideI
  252390. 21622N
  252391. 2/28/96VuStructure of LTMP and LPMP in Hydrocarbon Solution :  Assignment of Cyclic Trimer and Tetramer Conformational IsomersW
  252392. 1994X
  252393. 7949Y
  252394. 116 (17)
  252395. Boger, D. L.B
  252396. JACSC
  252397. DNA Alkylation 
  252398. 21623N
  252399. 2/28/96
  252400. CBI-TMI: Synthesis and Evaluation of a Key Analog of the Duocarmycins.  Validation of a Direct Relationship between Chemical Solvolytic Stability and Cytotoxic Potency and Conformation of the Structural Features Responsible for the Distinguishing Behavior of Enantiomeric Pairs of Agents
  252401. 1994X
  252402. 7996Y
  252403. 116 (18)
  252404. Hegedus, L. S.B
  252405. JACSC=Palladium Catalyzed Carbonylation
  252406. Organotin
  252407. Cuprate Addition
  252408. 21624N
  252409. 2/28/96V
  252410. Asymmetric Synthesis of a-Amino Acids by Copper Catalyzed Conjugate Addition of Grignard Reagents to Optically Active Carbamatoacrylates W
  252411. 1994X
  252412. 8126Y
  252413. 116 (18)
  252414. Nicolaou, K. C.B
  252415. JACSC%Carbanion
  252416. Aryl Lithium Rearrangement
  252417. 21625N
  252418. 2/28/96V
  252419. Total Synthesis of BalanolW
  252420. 1994X
  252421. 8402Y
  252422. 116 (18)
  252423. Negishi, E-I.B
  252424. JACSC"Annulation
  252425. Organoaluminum Reagent
  252426. 21626N
  252427. 2/28/96VATitanium Catalyzed Cascade Carboalumination of Dienes and TrienesW
  252428. 1994X
  252429. 8404Y
  252430. 116 (18)
  252431. West, F. G.B
  252432. C9Diazoketone
  252433. Stevens Rearrangement
  252434. Copper/ Rhodium CarbeneI
  252435. 21627N
  252436. 2/28/96VuPiperidines via Ammonium Ylide [1,2]-Shifts:  A Concise, Enantioselective Route to (-)-Epilupinine from Proline EsterW
  252437. 1994X
  252438. 8420Y
  252439. 116 (18)
  252440. Curran, D. P.B
  252441. JACSC)Radical Cyclization
  252442. Annulation
  252443. Organotin
  252444. 21628N
  252445. 2/28/96V
  252446. Substrate Controlled Group Selective Radical Cyclizations.  A New Strategy for Stereocontolled Transformations of Diastereomeric Reactive IntermediatesW
  252447. 1994X
  252448. 8430Y    116 (18) 
  252449. Sharpless, K. B.B
  252450. JACSC
  252451. Osmium Tetroxide
  252452. Oxidation
  252453. 21629N
  252454. 2/28/96V
  252455. Toward an Understanding of the High Enantioselectivity in the Osmium-Catalyzed Asymmetric Dihydroxylation. 2. A Qualitative Molecular Mechanics ApproachW
  252456. 1994X
  252457. 8470Y
  252458. 116 (19)
  252459. Quallich, G. J.B
  252460. JACSC
  252461. Enantioselective ReductionI
  252462. 21630N
  252463. 2/28/96VrA Comined Synthetic and ab Initio Study of Chiral Oxazaborolidines Structure and Enantioselectivity Relationships.W
  252464. 1994X
  252465. 8516Y
  252466. 116 (19)
  252467. Lautens, M.B
  252468. JACSC!Samarium
  252469. Organotin
  252470. Organosilicon
  252471. 21631N
  252472. 2/28/96V>Studies in the Directed Cyclopropanation of a-Allenic AlcoholsW
  252473. 1994X
  252474. 8526Y
  252475. 116 (19)
  252476. Roush, W. R.B
  252477. JACSC3Organnotin
  252478. Lewis Acid
  252479. Homoallylic Alcohol SynthesisI
  252480. 21632N
  252481. 2/28/96V
  252482. [(Z)-g-{Diisopropyllidene-a-D-mannopyranosyl)oxy]allyl]tributylstannane:  A New Chiral Reagent for the Asymmetric a-Hydroxyallylation of AldehydesW
  252483. 1994X
  252484. 8536Y
  252485. 116 (19)
  252486. Boger, D. L.B
  252487. JACSCHUllmann Aryl Ether Synthesis
  252488. Copper
  252489. Macrocyclization via amide formationI
  252490. 21633N
  252491. 2/28/96VSTotal Synthesis of Bouvardin, O-Methylbouvardin, and O-Methyl-N9-desmethylbouverdinW
  252492. 1994X
  252493. 8544Y
  252494. 116 (19)
  252495. Buchwald, S. L.B
  252496. JACSC@Annulation
  252497. Organotitanium 
  252498. Cyclopentenone Synthesis
  252499. Pauson KhandI
  252500. 21634N
  252501. 2/28/96VWDevelopement of a Titanocene Catalyzed Enyne Cyclization/ Isocyanide Insertion ReactionW
  252502. 1994X
  252503. 8593Y
  252504. 116 (19)
  252505. Chung, Y. K. B
  252506. C>Annulation
  252507. Organocobalt 
  252508. Cyclopentenone Synthesis
  252509. Pauson KhandI
  252510. 21635N
  252511. 2/28/96Vc(Indenyl)cobalt(I) Catalyzed Cocyclization of Alkyne, Alkene and Carbon Monoxide to CyclopentenonesW
  252512. 1994X
  252513. 8793Y
  252514. 116 (19)
  252515. Coleman, R. S.B
  252516. JACSC!Diels-Alder
  252517. Naphthalene SynthesisI
  252518. 21636N
  252519. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  252520. 1994X
  252521. 8795Y
  252522. 116 (19)
  252523. Coleman, R. S.B
  252524. JACSCABiaryl Cyanocuprate
  252525. Organocopper
  252526. Organolithium
  252527. Oxidative CouplingI
  252528. 21637N
  252529. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  252530. 1994X
  252531. 8795Y
  252532. 116 (19)
  252533. Coleman, R. S.B
  252534. JACSC*MnO2 Oxidative Phenoxy Radical CyclizationI
  252535. 21638N
  252536. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  252537. 1994X
  252538. 8795Y
  252539. 116 (19)
  252540. Denmark, S. E.B
  252541. CLChiral Aniline Synthesis
  252542. Organolithium
  252543. Chiral Ligand
  252544. Bis-Oxazoline
  252545. SparteineI
  252546. 21639N
  252547. 2/28/96V7Asymmetric Addition of Organolithium Reagents to IminesW
  252548. 1994X
  252549. 8797Y
  252550. 116 (19)
  252551. Townsend, C. A.B
  252552. JACSC
  252553. Enediyne AntibioticsI
  252554. 21640N
  252555. 2/28/96VbKinetic vs Thermodynamic Determinants in the Sequence Selectivity of DNA Cleavage by CalicheamicinW
  252556. 1994X
  252557. 8819Y
  252558. 116 (19)
  252559. Lautens, M. B
  252560. JACSCONickel Cyclooctadiene
  252561. Palladium Catalyzed Intramolecular Cyclization
  252562. AnnulationI
  252563. K+also see JACS 1994, 116, 8526 (this issue)
  252564. 21641N
  252565. 2/28/96VXStereochemical Control in Metal Catalyzed [3+2] Cycloadditions of MethylenecyclopropanesW
  252566. 1994X
  252567. 8821Y
  252568. 166 (19)
  252569. Koga, K.B
  252570. JACSC$Asymmetric Alkylation
  252571. Organolithium
  252572. 21642N
  252573. 2/28/96V
  252574. Catalytic Asymmetric Benzylation of Achiral Lithium Enolates Using a Chiral Ligand for Lithium in the Presence of a Achiral Ligand W
  252575. 1994X
  252576. 8829Y
  252577. 116 (19)
  252578. Carreira, E. M.B
  252579. CQAsymmetric Mukaiyama Aldol Reaction
  252580. Chiral Titanium Catalyst
  252581. Silyl Ketene AcetalsI
  252582. 21643N
  252583. 2/28/96V
  252584. Catalytic, Enantioselective Aldol Additions with Methyl and Ethyl Acetate O-Silyl Enolates:  A Chiral Tridentate Chelate as a Ligand for Titanium (IV)W
  252585. 1994X
  252586. 8837Y
  252587. 116 (19)
  252588. A    Luh, T-Y.B
  252589. JACSC*Dithioacetal
  252590. Dithioketal
  252591. Olefin Synthesis
  252592. 21644N
  252593. 2/28/96VdChelation Assistance in the Activation of Csp3-S Bonds in Nickel-Catalyzed Cross-Coupling Reactions W
  252594. 1994X
  252595. 8920Y
  252596. 116 (20)
  252597. Buchwald, S. L.B
  252598. JACSC7Organotitanium Hyride Reduction
  252599. Chiral Amine Synthesis
  252600. 21645N
  252601. 2/28/96V
  252602. 1. Catalytic Asymmetric Hydrogenation of Imines with a Chiral Titanocene Catalyst:  Scope and Limitations
  252603. 2. Kinetic Resolution of Racemic Disubstituted 1-Pyrrolines via Asymmetric Reduction  with a Chiral Titanocene CatalystW
  252604. 1994X
  252605. 8952, 9373Y
  252606. 116 (20)
  252607. Pirrung, M. C.B
  252608. JACSC3Organorhodium 
  252609. Rh catalyzed C-H Insertion ReactionsI
  252610. 21646N
  252611. 2/28/96
  252612. Electronic Effects in Dirhodium (II) Carboxylates.  Linear Free Energy Relationships in Catalyzed Decompositions of Diazo Compounds and CO and Isonitrile ComplexationW
  252613. 1994X
  252614. 8991Y
  252615. 116 (20)
  252616. Aube, J.B
  252617. JACSChPhotochemical Oxaziridine Rearrangement
  252618. Lactam Synthesis
  252619. Photochemistry
  252620. Bischler-Napieralski CyclizationI
  252621. 21647N
  252622. 2/28/96V
  252623. Symmetry-Driven Synthesis of Indole Alkaloids:  Asymmetric Total Synthesis of (+)-Yohimbine, (-)-Yohimbone, (-)-Yohimane, and (+)-Alloyohimbane W
  252624. 1994X
  252625. 9009Y
  252626. 116 (20)
  252627. Collum, D. B.B
  252628. JACSC$Li-6 NMR
  252629. N-15 NMR
  252630. LTMP StructureI
  252631. 21648N
  252632. 2/28/96V
  252633. 1. Lithium Dialkylamide Mixed Aggregation:  MNDO Comutational Study of Salt and Solvent Dependencies
  252634. 2. Lithium Dialkylamide Mixed Aggregation:  An NMR Spectroscopic Study of Hexamethylphosphoramide (HMPA)W
  252635. 1994X
  252636. 9187, 9198Y
  252637. 116 (20)
  252638. Jacobsen, E. N.B
  252639. JACSC;Epoxide Synthesis
  252640. Chiral Organomanganese Catalyst
  252641. OxidationI
  252642. 21649N
  252643. 2/28/96
  252644. V?Highly Enantioselective, Low Temperature Epoxidation of StyreneW
  252645. 1994X
  252646. 9333Y
  252647. 116 (20)
  252648. Corey, E. J.B
  252649. JACSC
  252650. Organotitanium
  252651. Grigard Reagent
  252652. 21650N
  252653. 2/28/96V
  252654. Catalytic Diastereoselective Synthesis of Cis-1,2-Disubstituted Cyclopropanols from Esters Using a Vicinal Dicarbanion EquivalentW
  252655. 1994X
  252656. 9345Y
  252657. 116 (20)
  252658. Meyers, A. G.B
  252659. JACSC5Enantioselective Alkylation
  252660. Reduction
  252661. Lithium EnolateI
  252662. 21651N
  252663. 2/28/96VMUse of Pseudoephedine as a Practical Chiral Auxilary for Asymmetric SynthesisW
  252664. 1994X
  252665. 9361Y
  252666. 116 (20)
  252667. McDonald, F. E.B
  252668. JACSC*Furan Synthesis
  252669. Molybdenum Carbene ComplexI
  252670. 21652N
  252671. 2/28/96VZMechanism of Molybdenum Pentacarbonyl-Catalyzed Cyclizations of Alkynols and Epoxyalkenes W
  252672. 1994X
  252673. 9363Y
  252674. 116 (20)
  252675. Nicolaou, K. C.B
  252676. JACSCHRadical Desulfurization
  252677. Oxocene Synthesis
  252678. Lewis Acid Induced CyclizationI
  252679. 21653N
  252680. 2/28/96V3Total Synthesis of Truncated Brevetoxin B [AFGHIJK]W
  252681. 1994X
  252682. 9371Y
  252683. 116 (20)
  252684. Paterson, IB
  252685. JACSCCMacrolactonization
  252686. Protecting Groups
  252687. Boron Enolates
  252688. Aldol ChemistryI
  252689. 21654N
  252690. 2/28/96V4Total Synthesis of Swinholide A and Hemiswinholide AW
  252691. 1994X
  252692. 9391Y
  252693. 116 (20)
  252694. Kagan, H. B.B
  252695. JACSI
  252696. 21655N
  252697. 2/28/96V)Nonlinear Effects in Asymmetric CatalysisW
  252698. 1994X
  252699. 9430Y
  252700. 116 (21)
  252701. Taber, D. F.B
  252702. JACSCDOrganozirconium Mediated Cyclization
  252703. Zirconium
  252704. Annulation
  252705. Diene
  252706. DiolI
  252707. 21656N
  252708. 2/28/96VpStereoselectivity in Intramolecular Diene Cycloaromatization :  A Combined Experimental and Theoretical ApproachW
  252709. 1994X
  252710. 9457Y
  252711. 116 (21)
  252712. Danheiser, R. L.B
  252713. JACSCuPhotochemical Annulation
  252714. Diazoketone
  252715. Alkyne
  252716. Phenol
  252717. Wolff rearrangement
  252718. [2+2] Cycloaddition
  252719. Electrocyclic Ring ClosureI
  252720. 21657N
  252721. 2/28/96V8Total Synthesis of the Phenalenone Diterpene SalvilenoneW
  252722. 1994X
  252723. 9471Y
  252724. 116 (21)
  252725. Houk, K. N.B
  252726. JACSC
  252727. Computational Chemistry
  252728. 21658N
  252729. 2/28/96
  252730. Theoretical Secondary Kinetic Isotope Effects and the Interpretation of Transition State Geometries. 2.  The Diels-Alder Reaction Transition State GeometryW
  252731. 1994X
  252732. 9675Y
  252733. Rodrigues, J. A. R.B
  252734. JACSC+Oxenium Ion Cyclization
  252735. Hypervalent Iodine
  252736. 21659N
  252737. 2/28/96VpSynthesis of Cularine and Sarcocapnine via Enium Ions and a New, Highly Diastereoselective Reductive MethylationW
  252738. 1994X
  252739. 9745Y
  252740. Negeshi, E-i
  252741. JACSC2Zirconium 
  252742. Organozirconium
  252743. Diene
  252744. Ketone
  252745. AnnulationI
  252746. 21660N
  252747. 2/28/96V@Nonconcerted paths for Reactions of Alkene Zirconocene ComplexesW
  252748. 1994X
  252749. 9751Y
  252750. Beak, PB
  252751. JACSC<Organolithium
  252752. Lithium
  252753. Carbanion
  252754. Chiral Ligand
  252755. OrganostannaneI
  252756. 21661N
  252757. 2/28/96V
  252758. Asymmetric Substitutions:  High and Opposite Enantioselective Alkyations of a Racemic Organolithium Intermediate in the Presence of (-)-SparteineW
  252759. 1994X
  252760. 9755Y
  252761. Mori, M.B
  252762. JACSC!Organonickel Mediated Annulation
  252763. Synthesis of 5-7 membered rings
  252764. 21662N
  252765. 2/28/96VnNovel Stereoselective Cylization via p-Allylnickel Complex Generated from 1,3-Diene and Hydride Nickel ComplexW
  252766. 1994X
  252767. 9771Y
  252768. Somfai, P.B
  252769. JACSC
  252770. Aziridine
  252771. CarbanionI
  252772. 21663N
  252773. 2/28/96V1Aza-[2,3] Wittig Rearrangement of VinylaziridenesW
  252774. 1994X
  252775. 9781Y
  252776. Weinreb, S. M.B
  252777. JACSCZOrganosilicon
  252778. Organostannane
  252779. Palladium Catalyzed Coulping
  252780. Lewis Acid Mediated Cyclization
  252781. KTMechanistically, reaction proceeds via a rare type of pericyclic concerted pathway. M
  252782. 21664N
  252783. 2/28/96VeTotal Synthesis of Papuamine via Stereospecific Intramolecular Imino Ene Reaction of an AllenylsilaneW
  252784. 1994X
  252785. 9789Y
  252786. Weinreb, S. M.B
  252787. JACSC,Organostannane
  252788. Palladium Catalyzed Coulping
  252789. K-See TL 1991, 32, 5681 and Chem. Lett. 1987, 5M
  252790. 21665N
  252791. 2/28/96VeTotal Synthesis of Papuamine via Stereospecific Intramolecular Imino Ene Reaction of an AllenylsilaneW
  252792. 1994X
  252793. 9791Y
  252794. Kobayashi, S.B
  252795. &CbAsymmetric Aldol Condensation
  252796. Chiral Amine Ligand
  252797. Organotin Enolate
  252798. Silyl Ketene Acetal
  252799. Lewis AcidI
  252800. 21666N
  252801. 2/28/96V
  252802. Highly Enantioselective Synthesis of Enantionmeric 2,3-Dihdroxy Thioesters by Using Similar Types of Chiral Sources Derived from L-ProlineW
  252803. 1994X
  252804. 9805Y
  252805. White, J. DB
  252806. JACSC1Lewis Acid Mediated Polyene Cyclization
  252807. KetoesterI
  252808. 21667N
  252809. 2/28/96V
  252810. Construction of the Stemodane Nucleus by a Hydroxyl-Directed Intramolecular Ene Reaction.  Total Synthesis of (
  252811. )-2-DesoxystemodineW
  252812. 1994X
  252813. 9912Y
  252814. White, J. D.B
  252815. JACSC
  252816. Samarium Iodide Barbier Reaction
  252817. SmI2 Reduction
  252818. Huang-Minlon Reduction of Ketone
  252819. Annulation
  252820. Hydroxy Aldehyde
  252821. Thermal Ene Reaction
  252822. Lewis AcidI
  252823. 21668N
  252824. 2/28/96V
  252825. Construction of the Stemodane Nucleus by a Hydroxyl-Directed Intramolecular Ene Reaction.  Total Synthesis of (
  252826. )-2-DesoxystemodineW
  252827. 1994X
  252828. 9912Y
  252829. Bach, R. D.B
  252830. JACSC1Diels-Alder Cycloaddition Reaction
  252831. Isobenzofuran
  252832. 21669
  252833. 2/28/96V
  252834. Synthesis of (
  252835. )-FredericamycinW
  252836. 1994X
  252837. 9921Y
  252838. Bach, R. D.B
  252839. JACSCRMercury Mediated Pinacol Rearrangement
  252840. Dithioacetal
  252841. Bis Silyl enol Ether
  252842. 1,3-DioneI
  252843. 21670N
  252844. 2/28/96V
  252845. Synthesis of (
  252846. )-FredericamycinW
  252847. 1994X
  252848. 9921Y
  252849. Bach, R. D.B
  252850. JACSC:Benzylic Lithium Carbanion
  252851. Cuprate
  252852. Organocuprate
  252853. AcylationI
  252854. 21671N
  252855. 2/28/96V
  252856. Synthesis of (
  252857. )-FredericamycinW
  252858. 1994X
  252859. 9921Y
  252860. Bach, R. D.B
  252861. JACSCHMichael Condensation
  252862. Lithium Carbanion
  252863. Annulation
  252864. Dieckmann CondensationI
  252865. 21672N
  252866. 2/28/96V
  252867. Synthesis of (
  252868. )-FredericamycinW
  252869. 1994X
  252870. 9921Y
  252871. Mark L. Trudell
  252872. Zhengming ChenB
  252873. Tet. Lett.CEazabicyclo
  252874. epibatidine
  252875. conduramine
  252876. [4+2] cycloaddition
  252877. pyrrole
  252878. TosMICI
  252879. Yields generally better than 80%
  252880. Ratio of A:B is 1:1 in 2 reported cases and 2:3 in one case
  252881. R1= H, CO2Me, COMe
  252882. R2= H, Me, Ph, CO2Me
  252883. R3= Me, t-Bu, Bn
  252884. 21673N
  252885. 2/28/96VASynthesis of Highly Functionalized 7-Azabicyclo[2.2.1]heptadienesW
  252886. 1994X
  252887. 9649Y
  252888. Heterocycle(N)
  252889. Azabicyclo
  252890. Viktor V. ZhandankinB
  252891. Tet. Lett.COtrimethylsilyl azide
  252892. azidoiodinanes
  252893. azidonation
  252894. azidotriflate
  252895. benziodoxol
  252896. azideI
  252897. 'K&paper describes prep of azidioiodinaneM
  252898. 21674N
  252899. 2/28/96V
  252900. Preparation and Chemistry of Stable Azidoiodinanes: 1-Azido-3,3-bis(trifluoromethyl)-3-(1H)- 1,2-benziodoxol and 1-Azido-1,2-benziodoxol-3-(1H)-oneW
  252901. 1994X
  252902. 9677Y
  252903. Amination
  252904. Azidonation
  252905. Franz-Peter MontfortsB
  252906. Tet. Lett.
  252907. A7a,b - unsaturated sulfone
  252908. pyrrole
  252909. TosMIC
  252910. 1,4 - addition
  252911. (KGOxone = 2KHSO3   KHSO4  K2SO4
  252912. Compares methods of van Leusen and BartonM
  252913. 21675N
  252914. 2/28/96
  252915. AAA useful Preparation of Pyrroles from a,b -  unsaturated Sulfones
  252916. 1994X
  252917. 9703Y
  252918. Heterocycle(N)
  252919. pyrroles
  252920. Jean d
  252921. AngeloB
  252922. Tet. Lett.C
  252923. Michael
  252924. asymmetric
  252925. imine
  252926. chiralI
  252927. 21676N
  252928. 2/28/96V
  252929. The Asymmetric Michael Reaction Using Chiral Imines under Neutral Conditions: Stereochemical Evidences in Support of Cyclic Transition StateW
  252930. 1994X
  252931. 9705Y
  252932. Michael
  252933. Asymmetric
  252934. Howard Alper
  252935. In Sik ChoB
  252936. Tet. Lett.CYHydrogenation
  252937. diene
  252938. 1 atm H2
  252939. monoene
  252940. cyclic
  252941. acyclic
  252942. selective
  252943. nitro
  252944. ester
  252945. ketoneI
  252946. *KBYields > 90%
  252947. w/ 4 mol% cat. and -20C for 10hr 95% yield of 6/4 A/BM
  252948. 21677N
  252949. 2/28/96V}Selective Hydrogenation of Simple and Functionalized Conjugated Dienes Using a Binuclear Palladium Complex Catalyst PrecursorW
  252950. 1995X    5673-5676Y
  252951. 36:32\
  252952. Hydrogenation  - dienea
  252953. GABRIEL WEATHERHEADy
  252954. Univ. Ottawa Canada
  252955. M.F. Semmelhack
  252956. W.R. EpaB
  252957. Tet. Lett.C
  252958. oxy-palladation
  252959. vinylation
  252960. tandem
  252961. intramolecular
  252962. hydroxy alkene
  252963. palladium
  252964. furan
  252965. pyran
  252966. Pd(Oac)2
  252967. copper chloride
  252968. cyclizationI
  252969. +K>yields >80%
  252970. alkenes include: CH2=CHCOMe, CH2=CHPh, CH2=CHCO2Me
  252971. 21678N
  252972. 2/28/96V/Catalytic Tandem Oxy-Palladation and VinylationW
  252973. 1993X    7205-7208Y
  252974. 34:45\
  252975. Palladium - Oxy-palladationa
  252976. GABRIEL WEATHERHEADy    princeton
  252977. Hans-Gunther SchmalzB    Angew IntC
  252978. metathasis
  252979. grubbs
  252980. schrock
  252981. ruthenium
  252982. molybdenum
  252983. catalysis
  252984. catalytic
  252985. cyclize
  252986. olefin
  252987. diene
  252988. ruthenium
  252989. enyne
  252990. dienyne
  252991. blechert
  252992. Fluviricin B Aglycon
  252993. Hoveyda
  252994. reviewI
  252995. short reviewM
  252996. 21679N
  252997. 2/28/96VlCatalytic Ring-Closing Metathasis: A New, Powerful Technique for Carbon-Carbon Coupling in Organic SynthesisW
  252998. 1995X    1833-1836Y
  252999. 34:17\
  253000. cyclization - metathesisa
  253001. GABRIEL WEATHERHEAD
  253002. Wolfgang HerrmannB    Angew IntCBheck
  253003. palladium
  253004. palladacycle
  253005. olefination
  253006. coupling
  253007. stable
  253008. high temp
  253009. addition of t-butyl ammonium salt is a second catalyst demonstrated.
  253010. Temp stability is approx 100C greater than traditional catalystsM
  253011. 21680N
  253012. 2/28/96VbPaladacycles as Structurally Defined Catalysts for the Heck Olefination of Chloro- and BromoarenesW
  253013. 1995X
  253014. 1844Y
  253015. 34:17
  253016. Palladium - Hecka
  253017. GABRIEL WEATHERHEAD
  253018. Suk-Ku KangB
  253019. Tet. Lett.C
  253020. Aryl Iodide
  253021. iodobenzene
  253022. Palladium Acetate
  253023. Pd(OAc)2
  253024. allylic alcohol
  253025. n-Bu3P
  253026. tributyl phosphine
  253027. hydroxy ketone
  253028. allylic diol
  253029. couplingI
  253030. .K'AgOAc gave a 6:4 ratio of both productsM
  253031. 21681N
  253032. 2/28/96VnPalladium-Catalyzed Arylation of Allylic Diols: Highly Selective Synthesis of Phenyl-Substituted Allylic DiolsW
  253033. 1995X    6287-6290Y
  253034. 36:35\"Palladium - Heck - Allyl - (0001).a
  253035. GABRIEL WEATHERHEAD
  253036. Shigetoshi TakahashiB
  253037. Tet. Lett.C
  253038. rhodium
  253039. carbonylation
  253040. indolone
  253041. quinolone
  253042. alkyne
  253043. aniline
  253044. cyclization
  253045. hydrogenation
  253046. carbon monoxide CO
  253047. water H2O
  253048. triethyl amine TEA
  253049. acetylene
  253050. acetylenicI
  253051. Temp for reaction ranges from 80C to 175C for 14hr
  253052. Yields ~ 80%
  253053. Best results from 4 eq of H2O @ 175C for 14hr  68% isolated yield
  253054. 2 is believed to be a result of hydrogenation of 3 with H2O as Hydrogen source
  253055. In absence of H2O and TEA @ 80C for 14hr, 85% ield of product 3 obtained
  253056. 21682
  253057. 2/28/96VXRhodium-Catalyzed Carbonylation of 2-Alkynlaniline: Synthesis of 1,3-Dihydroindol-2-onesW
  253058. 1995X    6243-6246Y
  253059. 36:35\"Carbonylation - Acetylene - (0001)a
  253060. GABRIEL WEATHERHEADy
  253061. Osaka
  253062. Kyoung Soon Kim
  253063. Liganag QianB
  253064. Tet. Lett.Cdguanidine
  253065. aniline
  253066. thiourea
  253067. mercury (II) chloride  HgCl2
  253068. copper (II) chloride  CuCl2
  253069. pyrroleI
  253070. 0KHwhen 2-chloropyridne is used with TEA as base, the bis adduct us formed.M
  253071. 21683N
  253072. 2/28/96V1Improved Method for the Preparation of GuanidinesW
  253073. 1993X    7677-7680Y
  253074. 34:48\
  253075. Amines - Guanidines - (0001)a
  253076. GABRIEL WEATHERHEADy
  253077. Bristol-Meyers Squibb
  253078. David B MacLean
  253079. Rahul VohraB
  253080. Tet. Lett.CSEnamine
  253081. Peterson
  253082. heterocycle
  253083. tryptamine
  253084. cyclization
  253085. TMS methyl
  253086. tetrahydro-carbolineI
  253087. 1K\overall yields range from 34% to 61%
  253088. Ar group = pyridyl, quinoline, isoquinoline derivativesM
  253089. 21684N
  253090. 2/28/96VaEnamine Precursors of 1-Substituted-1,2,3,4-Tetrahydro-B-carbolines by way of a Peterson ReactionW
  253091. 1993X    7673-7676Y
  253092. 34:48
  253093. 8\,Heterocycle(N) - Indole - Carboline - (0001)a
  253094. GABRIEL WEATHERHEADw
  253095. aldehyde -> alkeney
  253096. Hamilton Ontario
  253097. A. Peter Johnson et al.B
  253098. Tet. Lett.C
  253099. Peterson olefination
  253100. benzotriazole
  253101. metallation
  253102. silylation
  253103. iminoether
  253104. oxindole
  253105. photolysis
  253106. TMSCl
  253107. radical
  253108. adamantane
  253109. cyclizationI
  253110. 21685N
  253111. 2/28/96V`Novel Metallation of Benzotriazoles and its Utitlity in the Synthesis of 4-Substituted OxindolesW
  253112. 1995X    6321-5324Y
  253113. 36:35\+Heterocycle(N) - indole - oxindole - (0001)a
  253114. GABRIEL WEATHERHEADy
  253115. Leeds
  253116. :A%R. Menicagli
  253117. V. Guagano
  253118. S. SamaritaniB
  253119. Tet. Lett.Cv2-alkyltetrahydropyran-3-one
  253120. tetrahydropyrone
  253121. grignard
  253122. nitro
  253123. pyran
  253124. hydrolysis
  253125. michael
  253126. nitroalkenes
  253127. magnesium nitronateM
  253128. 21686N
  253129. 2/28/96VkOne-pot Synthesis of 2-Alkyltetrahydropyran-3-oness from 3-Nitro-5,6-Dihydro-4H-Pyran and Grignard ReagentsW
  253130. 1995X    9531-9532Y
  253131. 36:52a
  253132. GABRIEL WEATHERHEAD
  253133. ;A    W. SmadjaB
  253134. SynlettI
  253135. ReviewM
  253136. 21687N
  253137. 2/28/96
  253138. ;VcAcyclic Diastereofacial Selection in Intermolecular Racical Reactions Steric vs Electronic ControlsW
  253139. 1994X
  253140. no. 1
  253141. O. YonemitsuB
  253142. SynlettCJCarbohydrate Chemistry
  253143. Tetrahydropyran Synthesis
  253144. Tetrahydrofuran SynthesisI
  253145. 21688N
  253146. 2/28/96
  253147. Synthetic Studies of Halicondrin B, an Antitumor Polyether Macrolide Isolated From A Marine Sponge.  Stereoselective Synthesis of the C-1-C13 Fragment via Construction of the B acnd A Rings by Kinetically and Thermodynamically Controlled Intramolecular Michael Reactions 
  253148. 1994X
  253149. 38, 40,43, 46Y
  253150. no. 1
  253151. H. IshibashiB
  253152. SynlettCDPummerer Rearrangement
  253153. Sulfoxide
  253154. Electrophilic Aromatic SubstitutionI
  253155. 21689N
  253156. 2/28/96VKFirst Total Synthesis of the Benzopyranobenazepine Alkaloid (
  253157. )-ClavizepineW
  253158. 1994X
  253159. no. 1
  253160. J. SuffertB
  253161. SynlettCCPalladium Coupling
  253162. Bergman Reaction
  253163. Diradical
  253164. DNA Cleavage
  253165. EnediyneI
  253166. 21690N
  253167. 2/28/96
  253168. >ViThe Synthesis and Acid Induced Cycloaromatization of a Dienediyne Analog of Neocarzinostatine ChromophoreW
  253169. 1994X
  253170. no. 1
  253171. ?A    M. NakataB
  253172. SynlettC#Lewis Acid Catalyzed Cycloaddition
  253173. 21691N
  253174. 2/28/96VIThe Intramolecular Diels-Alder Reaction of a 14-Membered Diene-DienophileW
  253175. 1994X
  253176. J. BarluengaB
  253177. JOCC3Metal Halogen Exchange
  253178. Carbanion
  253179. Lithium
  253180. AlkylationI
  253181. 21692N
  253182. 2/28/96VUDirect Coupling of Functionalized Organolithium Compounds with Aryl and Vinyl HalidesW
  253183. 1993X
  253184. 5976Y
  253185. 58 (22)
  253186. G. A. MolanderB
  253187. JOCC\Enolate Alkylation
  253188. Titanium Catalyzed Michael Addition of AllylTrimethylsilane 
  253189. Oxonium Ion I
  253190. 21693N
  253191. 2/28/96V
  253192. Neighboring Group Participation in Lewis Acid Promoted [3+4] and [3+5] Annulations.  The Stereocontrolled Synthesis of Tricyclic EthersW
  253193. 1993X
  253194. 5931Y
  253195. 58 (22)
  253196. J. R. FalckB
  253197. JOCC3Alkylation
  253198. Sulfone
  253199. Annulation
  253200. Cyclization
  253201. ReductionI
  253202. 21694N
  253203. 2/28/96
  253204. BVbStereospecific Dehydrative Alkylation of Bis-Sulfones:  Synthesis of a Lesser Tea Tortix PheromoneW
  253205. 1993X
  253206. 5892Y
  253207. 58 (22)
  253208. D. KahneB
  253209. JACSCDEnediyne
  253210. Minor Groove of DNA
  253211. Bergman Cyclization
  253212. Diradical MechanismI
  253213. 21695N
  253214. 2/28/96VAStructural Characterization of a Calicheamicin-DNA Complex by NMRW
  253215. 1993X
  253216. 7954Y
  253217. 115 (18)
  253218. K. FukumotoB
  253219. JACSC
  253220. Lithium Reduction
  253221. Annulation
  253222. 21696N
  253223. 2/28/96V
  253224. Synthesis of Poylcyclic Cyclobutane Derivatives by Tandem Intramolecular Michael Aldol Reaction under two Complementary Conditions:  TBSOTf-TEA and TMSI-HMDS  
  253225. 1993X
  253226. 8107Y
  253227. 115 (18)
  253228. EA    P. MagnusB
  253229. JACSC
  253230. Pictet Spengler Condensation
  253231. Lawesson's Reagent
  253232. Intramolecular Michael Addtion
  253233. Sulfoxide
  253234. Pummerer Rearrangement to provide Cyclopropane
  253235. Annulation
  253236. Mercury (II) induced Cyclization
  253237. Wittig Reaction
  253238. 21697N
  253239. 2/28/96V8Synthesis of Strychnine and the Wieland-Gumlich AldehydeW
  253240. 1993X
  253241. 8116Y
  253242. 115 (18)
  253243. J. E. Leet
  253244. Enediyne
  253245. DNA CleavageI
  253246. 21698N
  253247. 2/28/96VAChemistry and Structure Elucidation of the Kedarcidin ChromophoreW
  253248. 1993X
  253249. 8432Y
  253250. 115 (18)
  253251. T. FukuyamaB
  253252. JACSC:Amide Coupling procedure
  253253. Annulation
  253254. Heterocycle Synthesis
  253255. 21699N
  253256. 2/28/96V"Total Synthesis of (-)-Tantazole BW
  253257. 1993X
  253258. 8449Y
  253259. 115 (18)
  253260. Fukuyama, TB
  253261. JACSC
  253262. Organolithium 
  253263. Carbanion
  253264. Cuprate
  253265. Wittig Reaction to afford an Allene
  253266. Asymmetric Mukaiyama Aldol Reaction
  253267. Triethylsilane Reduction
  253268. Takai Vinyl Iodide Synthesis
  253269. Palladium Coupling
  253270. Amide Coupling (BOP-Cl)
  253271. Beckmann Rearrangement
  253272. 21700N
  253273. 2/28/96V!Total Synthesis of (+)-LeinamycinW
  253274. 1993X
  253275. 8451Y
  253276. 115 (18)
  253277. Houk, K. N. B
  253278. JACSI
  253279. 21701N
  253280. 2/28/96VpThe Energetic Advantage of 5-exo Versus 6-endo Epoxide Openings:  A Preference Overwhelmed by Antibody CatalysisW
  253281. 1993X
  253282. 8453Y
  253283. 115 (18)
  253284. Sharpless, K. B. B
  253285. JACSC
  253286. Osmium Tetroxide
  253287. 21702N
  253288. 2/28/96V@Catalytic Asymmetric Dihydroxylation of Tetrasubstituted Olefins
  253289. 1993X
  253290. 8463Y
  253291. 115 (18)
  253292. Keck, G. E.B
  253293. JACSCLLewis Acid Catalyzed Addition of Allylstannane
  253294. organotin
  253295. Homoallylic AlcoholI
  253296. 21703N
  253297. 2/28/96V,Catalytic Asymmetric Allylation of AldehydesW
  253298. 1993X
  253299. 115 (18)
  253300. Danishefsky, S. J.B
  253301. JACSCGCarbohydrate
  253302. Glycoside Coupling
  253303. Zinc Triflate
  253304. Lewis Acid
  253305. Glycal EpoxideI
  253306. 21704N
  253307. 2/28/96V
  253308. Application of the Gylcal Assembly Strategy to the Synthesis of a Branched Oligosaccharide:  The First Synthesis of a Complex SaponinW
  253309. 1993X
  253310. 8473Y
  253311. 115 (18)
  253312. Shibasaki, M.B
  253313. JACSC>Zinc copper Couple
  253314. Organozinc
  253315. Palladium Coupling
  253316. Vinyl Iodide
  253317. 21705N
  253318. 2/28/96VoCatalytic Asymmetric Synthesis of Benzylic Quaternary carbon Centers.  An Efficient Synthesis of (-)-EptazocineW
  253319. 1993X
  253320. 8477Y
  253321. 115 (18)
  253322. Shibasaki, M.
  253323. JACSC6Heck Reaction
  253324. Palladium Coupling
  253325. BINAP
  253326. Pictet SpenglerI
  253327. 21706N
  253328. 2/28/96
  253329. NVoCatalytic Asymmetric Synthesis of Benzylic Quaternary carbon Centers.  An Efficient Synthesis of (-)-EptazocineW
  253330. 1993X
  253331. 8477Y
  253332. 115 (18)
  253333. Takahashi, T.B
  253334. JACSC Grignard Reagent
  253335. Allylic Ethers
  253336. 21707N
  253337. 2/28/96VPZirconium Catalyzed Highly Regioselective Carbon-Carbon Bond Formation ReactionsW
  253338. 1993X
  253339. 8485Y
  253340. 115 (18)
  253341. Gilbertson, S. R.B
  253342. JACSC
  253343. Organoiron Complexes
  253344. Iron 
  253345. 21708N
  253346. 2/28/96VcExo Selective Diels-Alder Reactions of a, b-Unsaturated Hexacarbonyl-Diiron Bridging Acyl ComplexesW
  253347. 8517Y
  253348. 115 (18)
  253349. Ireland, R. E.B
  253350. Ireland Claisen Rearrangement
  253351. DIBAL Reduction
  253352. Sharpless Epoxidation
  253353. Osmium Tetroxide
  253354. Cuprate
  253355. Hetero Diels-Alder Reaction
  253356. Dimethyldioxirane Oxidation
  253357. Radical Reduction with Phenyl Silane
  253358. Wittig Olefination
  253359. Chiral Crotyl Borane (H. C. Brown)
  253360. Hydroxyl Directed Hydrogenation
  253361. 21709N
  253362. 2/28/96
  253363. Convergent Synthesis of Polyether Ionophore Antibiotics:  Synthesis of the Spiroketal and Tricyclic Glycal Segments of MonensinW
  253364. 1993X
  253365. 7152, 7166Y
  253366. 115 (16)
  253367. Krafft, M. E.B
  253368. JACSCGCobalt Hexacarbonyl Alkyne Complex 
  253369. Annulation
  253370. Cyclopentenone SynthesisI
  253371. -Rate acceleration with NMO over the thermal reaction.  
  253372. -Further rate enhancement in the presence of heteroatoms in the homopropargylic or bishomopropargylic position
  253373. - NMR characterization of an intermediate cobalt complexM
  253374. 21710N
  253375. 2/28/96V_Effect of Coordinating Ligands on the Pauson Khand Cycloaddition:  Trapping of an Intermediate W
  253376. 1993X
  253377. 7199Y
  253378. 115 (16)
  253379. Suzuki, A.B
  253380. JACSC
  253381. Hydroboration
  253382. Vinyl Sulfde
  253383. 21711N
  253384. 2/28/96V
  253385. Palladium(0) Catalyzed Thioboration of Terminal Alkynes with 9-(Alkylthio)-9-borabicyclo[3.3.1] nonane Derivatives:  Stereoselective Synthesis of Vinyl Sulfides via the Thioboration Cross Coupling SequenceW
  253386. 1993X
  253387. 7219Y
  253388. 115 (16)
  253389. Gawley, R. E.B
  253390. TC6Organolithium
  253391. Carbanion
  253392. Organostannane
  253393. Amine SynthesisI
  253394. 3KK-a-aminolithium species stable upto -40
  253395. C in the presence of TMEDA (45 min)M
  253396. 21712N
  253397. 2/28/96V
  253398. 2-Lithio-N-methylpiperidine and 2-Lithio-N-methylpyrrolidine:  Configurationally and Chemically Stable Unchelated a-AminoorganolithiumsW
  253399. 1993X
  253400. 7515Y
  253401. 115 (16)
  253402. Molander, G. A.B
  253403. JACSCJChiral Secondary Alcohol
  253404. Enantioselective Borane Ketone Reduction
  253405. 1,4-DiolI
  253406. 21713N
  253407. 2/28/96V2Keto Borinate Reduction:  1,7-Asymmetric InductionW
  253408. 1993X
  253409. 7517Y
  253410. 115 (16)
  253411. Alper, HB
  253412. JACSC"Radical 
  253413. Carbonylation
  253414. Annulation
  253415. 21714N
  253416. 2/28/96V[The First Examples of Carbon Monoxide Trapping in a Manganese(III) Induced Oxidation SystemW
  253417. 1993X
  253418. 7543Y
  253419. 115 (16)
  253420. Wulff, W. D. B
  253421. JOCCAFischer Carbene Complexes
  253422. Enyne
  253423. Cyclobutane Synthesis
  253424. Annulation
  253425. 21715N
  253426. 2/28/96ViStereoselection in the Chromium mediated Intramolecular [2+2] Cycloadditions of Vinyl Ketenes and AlkenesW
  253427. 1993X
  253428. 5571Y
  253429. 58 (21)
  253430. XA    Luh, T-Y.B
  253431. JOCC9TBTH
  253432. Tetrahydropyran
  253433. Tetrahydrofuran
  253434. Cyclopropane
  253435. SiliconI
  253436. 21716N
  253437. 2/28/96V
  253438. Tandem Radical [2+1] Cycloaddition.  Remarkable Silyl Substituent Effect on the Chemoselectivity of the Radical Cyclization ReactionsW
  253439. 1993X
  253440. 5574Y
  253441. 58 (21)
  253442. YA    Luh, T-Y.B
  253443. JOCCEGrignard
  253444. Acetal Ring Opening
  253445. Nickel Catalyzed Coupling
  253446. Dithioacetals
  253447. 21717N
  253448. 2/28/96VwDifferentiation of Contiguous Hydroxyl Goups by Regioselective Conversion of Acetonides into tert-ButylHydroxyl Ethers W
  253449. 1993X
  253450. 5576Y
  253451. 58 (21)
  253452. Rawal, V. H.B
  253453. JOCC-Strychnos Alkaloids
  253454. Palladium
  253455. Annulation
  253456. HeckI
  253457. 21718N
  253458. 2/28/96V
  253459. An Unexpected Heck Reaction.  Inversion of Olefin Geometry Facilitated by the Apparent Intramolecular Carbamate Chelation of the s-Palladium IntermediateW
  253460. 1993X
  253461. 5583Y
  253462. 58 (21)
  253463. Mascarenas, J. L.B
  253464. JOCCNSilicon Tether
  253465. Annulation
  253466. Thermal Cyclization
  253467. Silyl Baeyer Villiger Oxidation
  253468. 21719N
  253469. 2/28/96
  253470. [VFTemporary Tethering Strategies for [5+2] Pyrone Alkene Cycloadditions W
  253471. 1993X
  253472. 5585Y
  253473. 58 (21)
  253474. Seconi, G.B
  253475. Amine Synthesis
  253476. Organocuprate
  253477. 21720N
  253478. 2/28/96V[Electrophilic Amination of Higher Order Cuprates with N, O-Bis(trimethylsilyl)hydroxylamineW
  253479. 1993X
  253480. 5620Y
  253481. 58 (21)
  253482. ]A    Beak, P.
  253483. JOCCEOrganolithium
  253484. Metallation
  253485. Carbanion
  253486. Alkylation
  253487. Aziridine
  253488. CyclopropaneI
  253489. 21721N
  253490. 2/28/96V
  253491. Intramolecular Cyclization of a-Lithioamine Synthetic Equivalents:  Convenient Syntheses of 3-, 5-, and 6-Membered Ring heterocyclic Nitrogen Compounds and Elaborations of 3-Membered Ring SystemsW
  253492. 1994X
  253493. 59 (2)
  253494. Marshall, J. E.B
  253495. JOCC,Homoallylic Alcohol
  253496. Carbanion
  253497. Organolithium
  253498. 21722N
  253499. 2/28/96V
  253500. Synthesis of the Pseudopterane 2,5-Furanocyclic Ring System by [2,3] Wittig Ring Contraction of Bridged Furan and Dihydrofuran Propargylic Ethers W
  253501. 1994X
  253502. 59 (2)
  253503. Burke, S. D.B
  253504. _CRCuprate
  253505. Allylic Mesylate
  253506. Grignard Reagent
  253507. Vinyl Iodide Synthesis
  253508. Silicon ChemistryI
  253509. Also Model System StudiedM
  253510. 21723N
  253511. 2/28/96V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  253512. 1994X
  253513. 59 (2)
  253514. Burke, S. D.B
  253515. JOCC]Ireland Claisen [3,3] Rearrangement
  253516. Sigmatropic Rearrangement
  253517. Carboxylic Acid
  253518. TetrahydropyranI
  253519. 21724N
  253520. 2/28/96V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  253521. 1994X
  253522. 59 (2)
  253523. Burke, S. D.B
  253524. JOCCyIntramolecular Diels-Alder Cycloaddition
  253525. Retro Diels-Alder
  253526. Annulation
  253527. Palladium Catalyzed Stille Coupling
  253528. Organostannane
  253529. 21725N
  253530. 2/28/96V>Total Synthesis of Ionophore Antibiotic X-14547A (Indanomycin)W
  253531. 1994X
  253532. 59 (2)
  253533. Danishefsky, S. J. B
  253534. Palladium Coupling
  253535. Annulation
  253536. PALLADIUM, INTRAMOLECULAR HECK ARYLATION OF ENOL ETHERS, HEXAHYDRO OXAZINE, ARYL IODIDE, FR 900482I
  253537. 21726N
  253538. 2/28/96
  253539. bV_A Remarkable Stereochemical Inversion in Some Heck Arylation Reactions. A Mechanistic Proposal W
  253540. 1994X
  253541. 59 (2)
  253542. Vedejs, E.B
  253543. JACSCNLewis Acid Catalyzed Sigmatropic Rearrangement
  253544. Titanium Catalyst
  253545. Chiral Amine
  253546. 21727N
  253547. 2/28/96VGAza Claisen Rearrangements Initiated by Acid Catalyzed Michael AdditionW
  253548. 1994X
  253549. 116 (2)
  253550. Hayashi, T.B
  253551. JACSC9Olefin Synthesis
  253552. BINAP Catalyst
  253553. p-Allyl Palladium SpeciesI
  253554. 21728N
  253555. 2/28/96VfCatalytic Asymmetric Reduction of Allylic Esters with Formic Acid Catalyzed by Palladium MOP ComplexesW
  253556. 1994X
  253557. 116 (2)
  253558. eA    Dai, L-X.B
  253559. JOCC>Copper (II) co-catalyst
  253560. Wacker Oxidation
  253561. Morpholine Synthesis
  253562. 21729N
  253563. 2/28/96VYPalladium(II) Catalyzed Synthesis of Optically Active Tetrahydro-1,4-oxazine Derivatives W
  253564. 1993X
  253565. 4775Y
  253566. 58 (18)
  253567. Knochel, P.B
  253568. JOCCJAlkylation
  253569. Diethyl Zinc
  253570. Organocopper
  253571. Higher Order Cuprate
  253572. Transmetalation
  253573. 21730N
  253574. 2/28/96
  253575. fV\Cross Coupling  between Functionalized Alkylcopper Reagents and Functionalized Alkyl HalidesW
  253576. 1993X
  253577. 4718Y
  253578. 58 (18)
  253579. Yamamoto, Y.B
  253580. Diels-Alder Reaction
  253581. Chelation Controlled Addition Allyl Stannane
  253582. Titanium Chloride Catalyst
  253583. Homoallylic Alcohol Synthesis
  253584. Ph3As and Ph3Sb
  253585. 21731N
  253586. 2/28/96VTMediation of the Reactivity of the Strong Lewis Acid TiCl4 by Complexation with XPh3W
  253587. 1993X
  253588. 4783Y
  253589. 58 (18)
  253590. Weinreb, S. M.B
  253591. JOCCiLewis Acid Catalyzed Cyclization
  253592. Vinyl Silane N-sulfonyliminium Ion Ring Closure
  253593. Aminocyclitol Synthesis
  253594. 21732N
  253595. 2/28/96V6An Approach to the Total Synthesis of (+)-LycoricidineW
  253596. 1993X
  253597. 4823Y
  253598. 58 (18)
  253599. Weinreb, S. M.B
  253600. JOCC>Heck Coupling
  253601. Palladium Catalyzed Annulation
  253602. Thallium Acetate
  253603. HKvanti elimination of PdH
  253604. REVIEW: Heck, R. F.; In Comprehensive Organic Synthesis: Trost, B. M., Ed.1991; Vol. 1, p 833.M
  253605. 21733N
  253606. 2/28/96V6An Approach to the Total Synthesis of (+)-LycoricidineW
  253607. 1993X
  253608. 4823Y
  253609. 58 (18)
  253610. Scott, W. J.B
  253611. Grignard Reagent
  253612. Zinc Reagent
  253613. 21734N
  253614. 2/28/96VPNickel Mediated Cross-Coupling of Unactivated Neopentyl Iodides with OrganozincsW
  253615. 1993X
  253616. 4866Y
  253617. 58 (18)
  253618. Harada, T.B
  253619. JOCC+Zinc Reagent
  253620. Palladium Coupling
  253621. Alkylation
  253622. 21735N
  253623. 2/28/96V
  253624. Reactions of 1,1-Dihaloalkenes with Triorganozincates:  A Novel Method for the Preparation of Alkenylzinc Species Associated with Carbon-Carbon Bond Formation  W
  253625. 1993X
  253626. 4897Y
  253627. 58 (18)
  253628. Weinreb, S. M.B
  253629. JOCCgIntramolecular Dipolar [3+2] Cycloaddition
  253630. Azomethine Ylide
  253631. Aziridine
  253632. Annulation
  253633. Flash Vacuum PyrolysisI
  253634. 21736N
  253635. 2/28/96VSDevelopment of a Strategy for the Synthesis of the Unusual Marine Alkaloid Sarain AW
  253636. 1993X
  253637. 4945Y
  253638. 58 (18)
  253639. Weinreb, S. M. B
  253640. JOCCyIntramolecular Allyl Silane N-tosyliminium Ion Cyclization
  253641. Ferric Chloride Lewis Acid
  253642. Annulation
  253643. Silicon Chemistry
  253644. AminolI
  253645. 21737N
  253646. 2/28/96VSDevelopment of a Strategy for the Synthesis of the Unusual Marine Alkaloid Sarain A
  253647. 1993X
  253648. 4945Y
  253649. 58 (18)
  253650. Paquette, L. A.B
  253651. JOCC;Anionic Oxy Cope
  253652. Oxidation
  253653. Vinyl Cerium Addition to Ketone
  253654. 21738N
  253655. 2/28/96V
  253656. Synthetic Equivalents of the Taxol C, D Ring System.  Examination of Nucleophilic Bicyclic Oxetanes and Less Strained Acetonide EquivalentsW
  253657. 1993X
  253658. 4952, 4963Y
  253659. 58 (18)
  253660. Giuliano, R. M.B
  253661. Annulation
  253662. [4+2] Cycloaddition
  253663. 21739N
  253664. 2/28/96VuDiastereofacial Selectivity of the Diels-Alder Reactions of Carbohydrate Derived Dienes and Their Carbocyclic AnalogsW
  253665. 1993X
  253666. 4979Y
  253667. 58 (18)
  253668. Curran, D. P.B
  253669. JOCC)Samarium Iodide Reduction
  253670. Radical Anion
  253671. 21740N
  253672. 2/28/96VOAdditive and Solvent Effects on SmI2 Reductions:  The Effects of Water and DMPUW
  253673. 1993X
  253674. 5008Y
  253675. 58 (18)
  253676. Rappoprt, H.B
  253677. JOCC1Annulation
  253678. Potassium Enolate
  253679. Aminoester SynthesisI
  253680. 21741N
  253681. 2/28/96
  253682. Chirospecific Synthesis of (1S,3R)-1-Amino-3-(hydroxymethyl)cyclopentane,  a Precursor for Carbocyclic Nucleoside Synthesis.  Intramolecular Aziridine CyclizationsW
  253683. 1993X
  253684. 5019Y
  253685. 58 (18)
  253686. Larock, R. C. B
  253687. 21742N
  253688. 2/28/96V`Palladium Catalyzed Annulation of 1,4-Dienes Using Ortho-Functionallity-Substituted Aryl HalidesW
  253689. 1993X
  253690. 4509Y
  253691. 58 (17)
  253692. sA    Kim, Y-H.B
  253693. JOCC)Enantioselective Reduction
  253694. Boron Hydride
  253695. 21743N
  253696. 2/28/96VxStereocontrolled Catalytic Asymmetric Reduction of Ketones with Oxazaborolidines Derived from New Chiral Amino Alcohols W
  253697. 1993X
  253698. 4511Y
  253699. 58 (17)
  253700. Larock, R. C.B
  253701. IodobenzaldehydeI
  253702. 21744N
  253703. 2/28/96VMSynthesis of Indenones via Palladium Catalyzed Annulation of Internal AlkynesW
  253704. 1993X
  253705. 4579Y
  253706. 58 (17)
  253707. Overman, L. E.B
  253708. Aza Cope Mannich Rearrangement
  253709. Lewis Acid
  253710. Iminium Ion Cyclization
  253711. Red-Al Reduction
  253712. Pictet Spengler Reaction
  253713. Osmium Tetroxide Oxidation of Si Enol Ether
  253714. 21745N
  253715. 2/28/96
  253716. Total Synthesis of Amaryllidaceae Alkaloids of the 5,11-Methanomorphanthridine Type.  Efficient Total Synthesis of (-)-Pancracine and (
  253717. )-Pancracine.W
  253718. 1993X
  253719. 4662Y
  253720. 58 (17)
  253721. Rajanbabu, T. V.
  253722. Nugent,W. A.B
  253723. JACSC+Titanium Complex
  253724. Deoxygenation of Epoxide
  253725. UK6inter- and intramolecular trapping of radical species.M
  253726. 21746N
  253727. 2/28/96V
  253728. Selective Generation of Free Radicals from Epoxides using a Transition Metal Radical.  A Powerful New Tool for Organic SynthesisW
  253729. 1994X
  253730. 116 (3)
  253731. Suzuki, K.B
  253732. JACSCNC-Glycoside coupling
  253733. Tetrahydrofuran Synthesis
  253734. Organosilane
  253735. Silver PerchlorateI
  253736. 21747N
  253737. 2/28/96V#Total Synthesis of the GilvocarcinsW
  253738. 1994X
  253739. 1004Y
  253740. 116 (3)
  253741. Suzuki, K.B
  253742. JACSC6Benzyne 
  253743. Diels-Alder Cycloaddition
  253744. Naphthol Synthesis
  253745. 21748N
  253746. 2/28/96V#Total Synthesis of the GilvocarcinsW
  253747. 1994X
  253748. 1004Y
  253749. 116 (3)
  253750. Suzuki, K.B
  253751. JACSC(Heck Coupling
  253752. Palladium
  253753. Biaryl coupling
  253754. 21749N
  253755. 2/28/96
  253756. yV#Total Synthesis of the GilvocarcinsW
  253757. 1994X
  253758. 1004Y
  253759. 116 (3)
  253760. Kuwajima, IB
  253761. Lewis Acid
  253762. Amine Synthesis
  253763. 21750N
  253764. 2/28/96VUHighly Stereoselective Ene Reaction of Aldimines with 2-(Alkylthio)allyl Silyl EthersW
  253765. 1994X
  253766. 59 (3)
  253767. Hoye, T. R.B
  253768. 21751N
  253769. 2/28/96VsEnolate and Other Carbon Nucleophile Alkylation Reactions Using 1,2-Cyclic Sulfates as Terminal Epoxide EquivalentsW
  253770. 1994X
  253771. 59 (3)
  253772. Whitesell, J., K.B
  253773. JOCC)Dialkyl Zinc Reagent
  253774. Chlorosulfite Ester
  253775. 21752N
  253776. 2/28/96VZAsymmetric Synthesis of Chiral Sulfinate Esters and Sulfoxides.  Synthesis of SulforaphaneW
  253777. 1994X
  253778. 59 (3)
  253779. Barluenga, J.B
  253780. JOCC7Bromine Lithium Exchange
  253781. Organostannane
  253782. Silyl MigrationI
  253783. 21753N
  253784. 2/28/96V
  253785. Preparation and Reactivity of New b-Nitrogen Functionalized Vinylic Organolithium Compounds from Secondary Aliphatic Allylamines W
  253786. 1994X
  253787. 59 (3)
  253788. Hawkins, J. M.B
  253789. ~C>Michael Addition
  253790. Lithium Enolate
  253791. Alkylation
  253792. b-Lactam SynthesisI
  253793. 21754N
  253794. 2/28/96VHAsymmetric Synthesis of Erythro and Threo a-Substituted b-Amino Esters  W
  253795. 1994X
  253796. 59 (3)
  253797. A    Anaya, J.B
  253798. Angew. Chem. Int. Ed. Engl. C;Radical Cyclization
  253799. Annulation
  253800. Dithiane
  253801. b-Lactam Synthesis
  253802. Chemical HighlightsM
  253803. 21755N
  253804. 2/28/96W
  253805. 1993X
  253806. Yamakawa, K. B
  253807. Chem. Pharm. Bull.CDTitanium Tetrachloride
  253808. Allylsilane Aldehyde Condensation
  253809. Annulation
  253810. Chemical HighlightsM
  253811. 21756N
  253812. 2/28/96W
  253813. 1993X
  253814. Iwao, M.
  253815. Watanabe, M.B
  253816. HeterocyclesCSStille Palladium Catalyzed Coupling
  253817. Indole Synthesis
  253818. Benzyne Cyclization
  253819. AnnulationI
  253820. Chemical HighlightsM
  253821. 21757N
  253822. 2/28/96W
  253823. 1993X
  253824. 1483Y
  253825. A    Stork, G.B
  253826. TLCYCationic Polyene Cyclization
  253827. Lewis Acid
  253828. Annulation
  253829. Radical Reduction
  253830. Epoxide Ring OpeningI
  253831. 21758N
  253832. 2/28/96
  253833. VyRegiospecificty in the Cyclization of 6-(1-Hydroxyalkyl) Geraniol Derivatives.  A Simple Route to the Taxol A Ring SystemW
  253834. 1994X
  253835. 1481Y
  253836. 35 (10)
  253837. Burke, S. D.B
  253838. TLC[Acetal Initiated Vinlysilane Terminated Polyene Cationic Cyclization
  253839. Annulation
  253840. Lewis Acid
  253841. 21759N
  253842. 2/28/96V\Enantioselective Synthesis of Nagilactone F Via Vinylsilane Terminated Cationic Cyclization W
  253843. 1994X
  253844. 1503Y
  253845. 35 (10)
  253846. Kise, N.B
  253847. TLC2Zinc Reagent
  253848. Lewis Acid
  253849. Reformatsky Reagents
  253850. ImineI
  253851. 21760N
  253852. 2/28/96V
  253853. Reaction of N-Acyl-a-methoxyamines with Organozinc Reagents.  A Convenient Method for the Synthesis of Homoallylamines and b-Amino EstersW
  253854. 1994X
  253855. 1561Y
  253856. 35 (10)
  253857. Hodgson, D. M.B
  253858. TLC,Annulation
  253859. Chromium Chloride
  253860. Nickel ChlorideI
  253861. 21761N
  253862. 2/28/96VjChromium (II) Mediated Nickel (II) Catalyzed Cylclisations of (Iodoaryl)- Substituted Alkynes and AlkynalsW
  253863. 1994X
  253864. 1601Y
  253865. 35 (10)
  253866. Shioiri, T. B
  253867. SynlettC.Homologation of Aryl Alkyl Ketones to Alkynes
  253868. 21762N
  253869. 2/28/96V
  253870. 1.  Extension of the Colvin Rearrangement Using Trimethylsilyldiazomethane.  A New Synthesis of Alkynes        2.  A New Synthesis of Aldehydes from Ketones Utlilizing TrimethylsilyldiazomethaneW
  253871. 1994X
  253872. 107, 109Y
  253873. no. 2
  253874. Whitby, R. J.B
  253875. SynlettC
  253876. Annulation
  253877. Enynes
  253878. 21763N
  253879. 2/28/96VnConvergent Synthesis of Aminobicyclo[3.3.0]octenes Using Zirconium Chemistry.  An Unusual Anti 1,3-Amine ShiftW
  253880. 1994X
  253881. no. 2
  253882. Laschat, S.B
  253883. SynlettC
  253884. Diels-Alder
  253885. 21764N
  253886. 2/28/96V
  253887. Intramolecular Hetero-Diels-Alder Reaction of Prolinol-Derived N-Arylamines Lewis Acid Dependent Reversal of the Diastereoselectivity W
  253888. 1994X
  253889. no. 2
  253890. Knolker, H-J.B
  253891. SynlettCAAnnulation
  253892. Silicon Chemistry
  253893. Lewis Acid
  253894. Baeyer-Villiger OxidationI
  253895. 21765N
  253896. 2/28/96V
  253897. [3+2] Cycloaddition of Allylsilanes, Part 5.  Synthesis of Bicyclo[3.3.0]octanes by Domino [3+2] Cycloadditions of Allysilanes and 3-Butyn-2-oneW
  253898. 1994X
  253899. Yamamoto, K.B
  253900. SynlettC1Silicon Chemistry
  253901. Palladium Chemistry
  253902. Annulation
  253903. 6-Endo CyclizationM
  253904. 21766N
  253905. 2/28/96VjA Novel Palladium (0) Catalyzed Cycloaddition of 2,7-Octadienyl Carbonate Containing an Allylsilane MoietyW
  253906. 1994X
  253907. no. 2
  253908. Kobayashi, S.B
  253909. SynlettCG Tin (II) Lewis Acid Mediated Asymmetric Aldol Reaction
  253910. Chiral Diamine
  253911. 21767N
  253912. 2/28/96VREnantioselective Synthesis of Both Diastereomers Including a-Alkoxy-b-methyl UnitsW
  253913. 1994X
  253914. no. 2
  253915. Suzuki, A.B
  253916. SynlettC
  253917. Boron Chemistry
  253918. 21768N
  253919. 2/28/96V
  253920. Synthesis of Allenes by Palladium Catalyzed Cross Coupling Reaction of Organoboron Compounds with Propargylic Carbonates:  Transmetallation of Organoboron Compounds with (Alkoxo)palladium Complexes Under Neutral Conditions W
  253921. 1994X
  253922. Garner, P.B
  253923. Oppolzer Camphor SultamI
  253924. 21769N
  253925. 2/28/96VVAuxiliary Controlled 1,3-Dipolar Cycloadditions of Chiral Stabilized Azomethine YlidesW
  253926. 1994X
  253927. 59 (1)
  253928. A    Bosch, J.B
  253929. JOCCIMetallation
  253930. Carbanion
  253931. Organotin
  253932. Organolithium
  253933. Protecting Group for IndoleI
  253934. 21770N
  253935. 2/28/96V{Preparation and Reactions of 1-(tert-Butyldimethylsilyl)-3-lithioindole.  Regioselective Synthesis of 3-Substituted IndolesW
  253936. 1994X
  253937. 59 (1)
  253938. Reissig, H-U.B
  253939. JOCC=Carbanion
  253940. Organolithium
  253941. Aminoaldehyde
  253942. Aminoalcohol Synthesis
  253943. 21771N
  253944. 2/28/96VnStereoselective Synthesis of 3(2H)-Dihydrofuranones by Addition of Lithiated methoxyallene to Chiral AldehydesW
  253945. 1994X
  253946. 59 (1)
  253947. Fukumoto, K.B
  253948. Sharpless Epoxidation
  253949. Titanium Chemistry
  253950. Radical 
  253951. Rearrangement
  253952. Cyclobutanone Synthesis
  253953. Mercury Trifluoroacetata
  253954. Methyl Cerium Addition to KetoneI
  253955. 21772N
  253956. 2/28/96V
  253957. A Remarkable Substituent Effect on the Enantioselectivity of Tandem Asymmetric Epoxidation and Enantiospecific Ring Expansion of Cyclopropylidene Alcohols:  A New Enantioconrolled Synthesis of (-)-Debromoaplysin and (-)-AplysinW
  253958. 1994X
  253959. 59 (1)
  253960. Fukumoto, K.B
  253961. C<Cyclopentenone Synthesis
  253962. Palladium Catalyzed Ring Expansion
  253963. 21773N
  253964. 2/28/96V
  253965. A Remarkable Substituent Effect on the Enantioselectivity of Tandem Asymmetric Epoxidation and Enantiospecific Ring Expansion of Cyclopropylidene Alcohols:  A New Enantioconrolled Synthesis of (-)-Debromoaplysin and (-)-AplysinW
  253966. 1994X
  253967. 59 (1)
  253968. A    Kishi, Y.B
  253969. Nickel Chloride
  253970. Chromium Chloride
  253971. Takai reaction
  253972. Propargylic Alcohol Synthesis
  253973. Carbohydrate Chemistry
  253974. Acid Catalyzed Epoxide Ring Closure
  253975. Tetrahydropyran SynthesisI
  253976. 21774N
  253977. 2/28/96VuPreferred Conformation of C-Glycosides.  12.  Synthesis and Conformational Analysis of a,a-,a,b-,and b,b-C-TrehalosesW
  253978. 1994X
  253979. 59 (1)
  253980. Hatanaka, M.B
  253981. JOCC*Intramolcular Wittig Reaction 
  253982. Annulation
  253983. 21775N
  253984. 2/28/96V
  253985. Allylidenetriphenylphosphorane as a Bifunctional Reagent:  Synthesis of Cyclopentenones and a,b-Unsaturated Ketones with (3-(Alkoxycarbonyl)-2-ethoxy-2-propenylidene)triphenylphosphoraneW
  253986. 1994X
  253987. 59 (1)
  253988. A    Hiroi, K.B
  253989. Alkylation
  253990. 21776N
  253991. 2/28/96VwThe Palladium Catalyzed Asymmetric a-Allylation of Carbonyl Compounds with Chiral Allyl Esters via Enamines and Imines W
  253992. 1994X
  253993. 59 (1)
  253994. Meyers, A. G.B
  253995. JACSC0Enediyne Antibiotics
  253996. Bergman Cyclization
  253997. RadicalI
  253998. 21777N
  253999. 2/28/96VdA Study of the Reaction of Calicheamicin g1 with Glutathione in thse Presence of Double Stranded DNAW
  254000. 1994X
  254001. 1255Y
  254002. 116 (4)
  254003. Sharpless, K. B.B
  254004. JACSI
  254005. 21778N
  254006. 2/28/96V{Toward an Understanding of the High Enantioselectivity in the Osmium Catalyzed Asymmetric Dihydroxylation (AD). 1. KineticsW
  254007. 1994X
  254008. 1278Y
  254009. 116 (4)
  254010. Yamamoto, H.B
  254011. JACSC
  254012. Chiral Boron ComplexI
  254013. 21779N
  254014. 2/28/96V\Br
  254015. nsted Acid Assisted Chiral Lewis Acid  (BLA) Catalyst for Asymmetric Diels-Alder ReactionW
  254016. 1994X
  254017. 1561Y
  254018. 116 (4)
  254019. Shibasaki, M.B
  254020. JACSI
  254021. 21780N
  254022. 2/28/96VYCatalytic Asymmetric Michael Reactions Promoted by a Lithium Free Lanthanum BINOL Complex
  254023. 1994X
  254024. 1569Y
  254025. 116 (4)
  254026. Nicolaou, K. C.B
  254027. JACSC
  254028. McMurry Coupling
  254029. Diol Synthesis
  254030. Titanium  Chemistry
  254031. Sharpless Epoxidation
  254032. Shapiro Reaction
  254033. Vinyl Lithium Species
  254034. Carbanion
  254035. PCC Allylic Oxidation
  254036. AnnulationI
  254037. a) Review:  "Chemistry and Biology of Taxol"  Nicolaou, K. C. Angew. Chem. Int. Ed. Engl. 1994, 33, 15-44 
  254038. b) For a Total Synthesis of Taxol see:  Nicolaou, K. C. Nature, 1994, 367, 630
  254039. 21781N
  254040. 2/28/96V
  254041. Synthesis of Novel TaxoidsW
  254042. 1994X
  254043. 1591Y
  254044. 116 (4)
  254045. Holton, R. A.B
  254046. JACSC
  254047. Chan Rearrangement
  254048. Intramolecular Acylation
  254049. Aldol Reaction
  254050. Samarium Iodide Reduction
  254051. Chiral Davis Reagent
  254052. Oxidation of  Li Enolate with OxaziridineI
  254053. 21782N
  254054. 2/28/96VCFirst Total Synthesis of Taxol. 1.  Functionalization of the B RingW
  254055. 1994X
  254056. 1597Y
  254057. 116 (4)
  254058. Holton, R. A.B
  254059. Dieckmann Cyclization to b-ketoester Annulation
  254060. Decarboxylation (PhSK)
  254061. Dehydration Burgess Reagent
  254062. Osmium Tetroxide
  254063. Oxetane Ring Synthesis
  254064. Oxidation of K Enolate to Hydroxy-ketone
  254065. Benzeneselenic Anhydride I
  254066. 21783N
  254067. 2/28/96VDFirst Total Synthesis of Taxol.  2.  Completion of the C and D RingsW
  254068. 1994X
  254069. 1599Y
  254070. 116 (4)
  254071. Pederson, S. F.B
  254072. JACSC9Diol Synthesis
  254073. Vanadium Chemistry
  254074. Aminoalcohol Synthesis
  254075. 21784N
  254076. 2/28/96V
  254077. Pinacol Cross Coupling of 2-[N-(Alkoxycarbonyl)amino] Aldehydes and Aliphatic Aldehydes by [V2Cl3(THF)6]2[Zn2Cl6].  Synthesis of syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-DiolsW
  254078. 1994X
  254079. 1316Y
  254080. 116 (4)
  254081. Aggarwal, V. K.B
  254082. Angew. Chem. Int. Ed. Engl. C
  254083. Asymmetric Deprotonation
  254084. ReviewM
  254085. 21785N
  254086. 2/28/96VkEnantioselective Transformations and Racemization Studies of Heteroatom Substituted Organolithium CompoundsW
  254087. 1994X
  254088. Nicolaou, K. C.B
  254089. Angew. Chem. Int. Ed. Engl.C,Enediyne Antiobiotic
  254090. DNA Cleavage
  254091. Diradical
  254092. 21786N
  254093. 2/28/96V
  254094. Calicheamicin:  A Rationally Designed Molecule with Extremely Potent and Selective DNA Cleaving Properties and Apoptosis Inducing ActivityW
  254095. 1994X
  254096. Aurrecoechea, J. M.B
  254097. JOCC%Annulation
  254098. Tertiary Alcohol SynthesisI
  254099. 21787N
  254100. 2/28/96V
  254101. Synthesis of Homopropargyl Cycloalkanols by Palladium Catalyzed Samarium Iodide Promoted Intramolecular Coupling of AlkynylEsters with Aldehydes and Ketones W
  254102. 1994X
  254103. 59 (4)
  254104. Denmark, S. E.B
  254105. 21788N
  254106. 2/28/96VqInvestigations on Transition State Geometry in the Lewis Acid - (Mukaiyama) and Fluoride Promoted Aldol ReactionsW
  254107. 1994X
  254108. 59 (4)
  254109. Shibasaki, M.B
  254110. JOCC<Intramolecular Chromium Complex      Cyclization
  254111. Annulation
  254112. 21789N
  254113. 2/28/96V
  254114. 1994X
  254115. 59 (4)
  254116. Paquette, L. A.B
  254117. Anionic Oxy Cope RearrangementI
  254118. 21790N
  254119. 2/28/96VoExploratory Synthetic Studies Involving the Tricyclo[9.3.3.0]tetradecane Ring System Peculiar to the Cyathins
  254120. 1994X
  254121. 59 (4)
  254122. Paquette, L. A.B
  254123. Radical Cyclization
  254124. AnnulationI
  254125. 21791N
  254126. 2/28/96VpExploratory Synthetic Studies Involving the Tricyclo[9.3.3.0]tetradecane Ring System Peculiar to the Cyathins
  254127. 1994X
  254128. 59 (4)
  254129. Tachibana, K.B
  254130. JOCC>Epoxide Ring Opening
  254131. Oxepane Ring Synthesis
  254132. 7-Endo CyclizationI
  254133. 21792N
  254134. 2/28/96V\Synthetic Studies toward Ciguatoxin.  Stereocontrolled Construction of the KLM Ring FragmentW
  254135. 1994X
  254136. 59 (4)
  254137. Malacria, M.B
  254138. JOCC1Annulation
  254139. [2+1] Radical Cyclization
  254140. CyclopropaneI
  254141. 21793N
  254142. 2/28/96V@A New Rare Example of Cyclopropanation in Free Radical ChemistryW
  254143. 1994X
  254144. 59 (4)
  254145. Shea, K. J.
  254146. TLC_Taxol Intermediate
  254147. Ireland Claisen Rearrangement
  254148. Organolithium
  254149. Carbanion 
  254150. Vinyl Lithium SpeciesI
  254151. 21794N
  254152. 2/28/96VbSynthesis of a C-1 Epi Taxinine Intermediate Using the Type 2 Intramolecular Diels-Alder Approach W
  254153. 1994X
  254154. 1317Y
  254155. 35 (9)
  254156. Trost, B. M.B
  254157. C1Annulation
  254158. Palladium Catalyzed Cyclization
  254159. EneyneI
  254160. 21795N
  254161. 2/28/96VOA Novel Cycloalkylation of 1,6- and 1,7-Enynes with Stabilized Pronucleophiles W
  254162. 1994X
  254163. 1361Y
  254164. 35 (9)
  254165. Whitby, R. J.B
  254166. TLC9Annulation
  254167. Insertion of Isocyanide into Zirconium ComplexI
  254168. 21796N
  254169. 2/28/96V8Synthesis of Cyclopentylamines using Zirconium ChemistryW
  254170. 1994X
  254171. 1445Y
  254172. 35 (9)
  254173. Molina, P.B
  254174. TLC=Aza Wittig
  254175. Electrocyclic Ring Closure
  254176. Pyridine Ring SynthesisI
  254177. 21797N
  254178. 2/28/96V@A Straightforward and Practical Formal Synthesis of LavendamycinX
  254179. 1453Y
  254180. 35 (9)
  254181. Enholm, E. J.B
  254182. TL CRSamarium Iodide
  254183. Annulation 
  254184. Aldol Reaction of Samarium Enolate
  254185. Radical CyclizationI
  254186. 21798N
  254187. 2/28/96VHSequential SmI2 Promoted One and Two Electron Reactions of Carbohyrates W
  254188. 1994X
  254189. 1627Y
  254190. 35 (11)
  254191. Crimmins, M.T. B
  254192. TLC.Silicon Tethered Photocyclization
  254193. Cyclobutane
  254194. 21799N
  254195. 2/28/96V;Siloxanes as Temporary Tethers in [2+2] PhotocycloadditionsW
  254196. 1994X
  254197. 1657Y
  254198. 35 (11)
  254199. Engler, T. A.B
  254200. TLC!Lewis Acid 
  254201. Stilbene
  254202. BenzoquinoneI
  254203. 21800N
  254204. 2/28/96V
  254205. Evaluation of a Synthetic Route to e-Viniferin Based on a New Method for the Stereoselective Preparation of 2,3-Diaryl-2,3-DihydrobenzofuransW
  254206. 1994X
  254207. 1661Y
  254208. 35 (11)
  254209. Knolker, H-J.B
  254210. TLC!Carbazole
  254211. Indole Ring Synthesis
  254212. Stiochiometric in Palladium(II)M
  254213. 21801N
  254214. 2/28/96V5Palladium Promoted Synthesis of a 7-DeoxyprekinamycinW
  254215. 1994X
  254216. 1695Y
  254217. 35 (11)
  254218. Kagan, H. B.B
  254219. TLC&Acid Chloride
  254220. a-Hyroxyketone SynthesisI
  254221. 21802N
  254222. 2/28/96VLSamarium Iodide in THP:  Preparation and some Reactions in Organic ChemistryW
  254223. 1994X
  254224. 1723Y
  254225. 35 (11)
  254226. Uemura, S.B
  254227. TLC Michael Type Conjugate Addition
  254228. KGNaBPh4 + AcOH  --->  Ph3B + PhH + NaOAc
  254229. Also see JOC 1995, 60 (4), 883M
  254230. 21803N
  254231. 2/28/96V
  254232. Antimony(III) Chloride as An Efficient Catalyst for Palladium Catalyzed Hydrophenylation of a,b-Unsaturated Ketones and AldehydesW
  254233. 1994X
  254234. 1739Y
  254235. 35 (11)
  254236. Bach, T.
  254237. Angew. Chem. Int. Ed. Engl.CWSilyl Eonol Ether
  254238. Organotin
  254239. Organosilane
  254240. Chiral Lewis Acid Catalyst
  254241. Homoallylic AlcoholI
  254242. ReviewM
  254243. 21804N
  254244. 2/28/96VTCatalytic Enantioselective C-C Coupling -Allyl Transfer and Mukaiyama Aldol ReactionW
  254245. 1994X
  254246. 33 (4)
  254247. Meyers, A. G.B
  254248. JACSC
  254249. Enediyne AntibioticsI
  254250. 21805N
  254251. 2/28/96V
  254252. DNA Cleavage by Neocarzinostatin Chromophore.  Establishing the Intermediacy of Chromophore-Derived Cumulene and Biradical Species and Their Role in Sequence Specific Cleavage.W
  254253. 1994X
  254254. 1670Y
  254255. 116 (5)
  254256. Rychnovsky, S. D.B
  254257. JACSC
  254258. Organolithium 
  254259. Alkylation of a-Lithio-nitriles
  254260. Noyori Asymmetric Hydrogenation
  254261. Intramolecular Horner Emmons Wittig Rxn
  254262. CyanohydrinI
  254263. 21806N
  254264. 2/28/96V:Convegent Synthesis of the Polyene Macrolide (-)-RoxaticinW
  254265. 1994X
  254266. 1753Y
  254267. 116 (5)
  254268. Paquette, L. A.B
  254269. JACSC    Oxy-Cope I
  254270. 21807N
  254271. 2/28/96V
  254272. Tandem Cope Cope RearrangementsW
  254273. 1994X
  254274. 1776Y
  254275. 116 (5)
  254276. Baldwin, J. E. B
  254277. Aldol Reaction
  254278. Lewis AcidI
  254279. 21808N
  254280. 2/28/96V5Total Synthesis of (+)-Lactacystin from (R)-GlutamateW
  254281. 1994X
  254282. 2139Y
  254283. 116 (5)
  254284. Roush, W. R.B
  254285. JACSC
  254286. Crotyl Borane
  254287. 21809N
  254288. 2/28/96V
  254289. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  254290. 1994X
  254291. 2151Y
  254292. 116 (5)
  254293. Roush, W. R.B
  254294. JACSC$Conjugate Addition
  254295. Grignard Reagent
  254296. 21810N
  254297. 2/28/96V
  254298. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  254299. 1994X
  254300. 2151Y
  254301. 116 (5)
  254302. Roush, W. R.B
  254303. JACSC
  254304. Triethyl Aluminum AlkylationI
  254305. 21811N
  254306. 2/28/96V
  254307. Application of h4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol:  Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)W
  254308. 1994X
  254309. 2151Y
  254310. 116 (5)
  254311. Greene, A. E.B
  254312. C/Cyclopentenone Synthesis
  254313. Cobalt Alkyne Complex I
  254314. 21812N
  254315. 2/28/96VtA Dual Function, Highly Efficient Chiral Chiral Controller for Stereoselective Intermolecular Pauson Khand ReactionsW
  254316. 1994X
  254317. 2153Y
  254318. 116 (5)
  254319. Vedejs, E.B
  254320. JACSI
  254321. 21813N
  254322. 2/28/96VaDeracemization via Highly Enantioselective Enolate Protonation Using a Chiral Aniline as the AcidW
  254323. 1994X
  254324. 2172Y
  254325. 116 (5)
  254326. Trost, B. M.B
  254327. JACSC(Palladium
  254328. Cyclopropane
  254329. Enyne
  254330. Annulation
  254331. 21814N
  254332. 2/28/96VJA Cycloaddition Approach to Cyclopentenes via Metalladienes as 4
  254333.  PartnersW
  254334. 1994X
  254335. 2183Y
  254336. 116 (5)
  254337. Marco-Contelles, J.B
  254338. JOCC&Annulation 
  254339. Alkyne
  254340. Tributyltin HydrideI
  254341. 21815N
  254342. 2/28/96VY6-endo-dig Free Radical Carbocyclizations:  A New Strategy for the Synthesis of CyclitolsW
  254343. 1994X
  254344. 1234Y
  254345. 59 (6)
  254346. Clive, D. L. J.B
  254347. JOCC5Annulation
  254348. Cobalt Chemistry
  254349. Cyclopentenone Synthesis
  254350. 21816N
  254351. 2/28/96
  254352. VkFormation of Angularly Fused Triquinanes by Successive Use of the Pauson Khand Reaction and Radical ClosureW
  254353. 1994X
  254354. 1396Y
  254355. 59 (6)
  254356. Kise, N.B
  254357. JOCC?Electrochemistry
  254358. Annulation
  254359. Reduction
  254360. Radical Anion CyclizationI
  254361. 21817N
  254362. 2/28/96VJElectroreductive Intramolecular Coupling of Nonconjugated Aromatic KetonesW
  254363. 1994X
  254364. 1407Y
  254365. 59 (6)
  254366. A    Padwa, A.B
  254367. JOCC!Rhodium Carbene Complex
  254368. ReductionI
  254369. 21818N
  254370. 2/28/96V
  254371. Studies on the Intramolecular Cycloaddition Reaction of Mesoionics Derived From the Rhodium (II) Catalyzed Cyclization of DiazoimidesW
  254372. 1994X
  254373. 1418Y
  254374. 59 (6)
  254375. Lee, E.B
  254376. Annulation
  254377. Radical Anion
  254378. 21819N
  254379. 2/28/96V`Reductive Cyclization of Ketones Tethered to Activated Olefins Mediated by Magnesium in MethanolW
  254380. 1994X
  254381. 1428Y
  254382. 59 (6)
  254383. Marshall, J. A.B
  254384. Oxidation
  254385. Epoxidation
  254386. 21820N
  254387. 2/28/96V\Enantioselective Synthesis of Carbohydrate Precursors via 1,2:2,3-Bis-Epoxide Intermediates
  254388. 1994X
  254389. 1457Y
  254390. 59 (6)
  254391. Kanemasa, S.B
  254392. JACSC
  254393. Isoxazoline
  254394. Grignard Reagent
  254395. 21821N
  254396. 2/28/96V
  254397. First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions.  High Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols W
  254398. 1994X
  254399. 2324Y
  254400. 116 (6)
  254401. Yamazaki, S.B
  254402. JACSCMSilicon Chemistry
  254403. Selenium Chemistry
  254404. Lewis Acid
  254405. Cyclopropane Synthesis
  254406. Enone
  254407. 21822N
  254408. 2/28/96Vg[2+1] Cycloaddition of Seleno-2-silylethenes.  Selenium Assisted 1,2-Silicon Shift for CyclopropanationW
  254409. 1994X
  254410. 2356Y
  254411. 116 (6)
  254412. Denmark, S. E.B
  254413. JACSC
  254414. Lithium CarbanionI
  254415. 21823N
  254416. 2/28/96V
  254417. Structure and Dynamics of Phosphorus (V) Stabilized Carbanions:  A Comparison of Theoretical, Crystallographic, and Solution StructuresW
  254418. 1994X
  254419. 2437Y
  254420. 116 (6)
  254421. Rawal, V. H.B
  254422. JACSCGReduction
  254423. Paterno Buchi Reaction
  254424. Diels-Alder
  254425. Radical Trapping Reaction
  254426. 21824N
  254427. 2/28/96
  254428. A General Strategy  for Increasing Molecular Complexity:  Photocycloaddition Fragmentation Route to Functionalized Di- and TriquinanesW
  254429. 1994X
  254430. 2613Y
  254431. 116 (6)
  254432. Paterson, I.B
  254433. JACSC0Allylsilane
  254434. Lewis Acid
  254435. Aldol Reaction
  254436. Reduction
  254437. 21825N
  254438. 2/28/96V$Total Syhthesis of (-)-Preswinolide
  254439. 1994X
  254440. 2615Y
  254441. 116 (6)
  254442. Hoye, T.B
  254443. JACSI
  254444. 21826N
  254445. 2/28/96V<A Total Synthesis of (+)-Xestospongin A/ (+)-Araguspongine DW
  254446. 1994X
  254447. 2617Y
  254448. 116 (6)
  254449. Rychnovsky, S. D.B
  254450. JACSCTAlkylation
  254451. Lithium Carbanion 
  254452. Cyanohydrin
  254453. Grignard Reagent for Conjugated Diene PrepI
  254454. 21827N
  254455. 2/28/96Vz1. Rapid Construction of the Roflamycoin System
  254456. 2. Stereochemical Assignment of Roflamycoin by C-13 NMR Acetonide AnalysisW
  254457. 1994X
  254458. 2621, 2623Y
  254459. 116 (6)
  254460. Meyers, A. I.B
  254461. JACSC%Alkylation
  254462. Lithium Enolate
  254463. ThiolactamI
  254464. 21828N
  254465. 2/28/96
  254466. Thio Claisen Rearrangements.  An Asymmetric Synthesis of 4,4-Disubstituted Cyclohexenones with Vicinal Quaterary and Tertiary StereocentresW
  254467. 1994X
  254468. 2633Y
  254469. 116 (6)
  254470. Kita, Y.B
  254471. JOC C
  254472. Lewis Acid
  254473. Nitrile Synthesis
  254474. 21829N
  254475. 2/28/96VhAn Unprecedented Cleavage of the b-Lactam ring :  Stereoselective Synthesis of Chiral b-Amido Cyanides 
  254476. 1994X
  254477. 59 (5)
  254478. Momose, T.B
  254479. JOCC2Cuprate Chemistry
  254480. Conjugate Addition
  254481. Organocopper
  254482. 21830N
  254483. 2/28/96V
  254484. Asymmetric Synthesis of the Indolizidine Alkaloids 207A, 209B, and 235B':  6-Substituted 2,3-Didehydropiperidine-2-carboxylate as a Versatile Chiral Building BlockW
  254485. 1994X
  254486. 59 (5)
  254487. Dittmer, D. C.B
  254488. JOCC0Super Hydride 
  254489. Boron Hydride Reduction
  254490. TelluriumI
  254491. K4-Te and super hydride produces telluride ion ( Te2-)M
  254492. 21831N
  254493. 2/28/96V_Concomitant Epoxide Deoxygenation and Deacylation of Glycidyl Acetates Induced by Telluride IonW
  254494. 1994X
  254495. 1004Y
  254496. 59 (5)
  254497. Feldman, K. S.B
  254498. Annulation
  254499. Organostannane
  254500. 21832N
  254501. 2/28/96V
  254502. Thoamide and Thioester Cyclopentane Synthesis via Trimethyltin Radical Catalyzed Alkenylation of Substituted (Thiocarbonyl)cyclopropanesW
  254503. 1994X
  254504. 1129Y
  254505. 59 (5)
  254506. Liebeskind, L. S.B
  254507. Rearrangement
  254508. 21833N
  254509. 2/28/96V
  254510. A Method for the Stereoselective Construction of 4-Alkoxy -5-Alkylidenecyclopentenones by the Tandem Ring Expansion-Functionalization of 1-Alkynylcyclobutenols Using a Palladium Mercury Cocatalytic SystemW
  254511. 1994X
  254512. 1149Y
  254513. 59 (5)
  254514. Mulzer, J.B
  254515. JOCCoIreland Claisen Rearrangement
  254516. Enantioselective Diethyl Zinc Addition
  254517. Clelate Cram Griganrd Addition
  254518. Osmylation
  254519. 21834N
  254520. 2/28/96VTStereoselective Synthesis of the Bis-tetrahyrrofuran fragment (C1-C-9) of AsteltoxinW
  254521. 1994X
  254522. 1160Y
  254523. 59 (5)
  254524. Guindon, Y.B
  254525. JOCCNTributyl Tin Hydride
  254526. Boron Lewis Acid Mediated Ring Opening
  254527. IodoetherificationI
  254528. 21835N
  254529. 2/28/96
  254530. Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals.  Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction:  Synthesis of the C17-C22 Subunit of Ionomycin  W
  254531. 1994X
  254532. 1166Y
  254533. 59 (5)
  254534. Charette, A. B.B
  254535. JACSC#Cyclopropane
  254536. Chiral Lewis Acid
  254537. ZincI
  254538. 21836N
  254539. 2/28/96VtDesign of Amphoteric Bifunctional Ligands to the Enantioselective Simmons-Smith Cyclopropanation of Allylic AlcoholsW
  254540. 1994X
  254541. 2651Y
  254542. 116 (6)
  254543. Paquette, L. A.B
  254544. JACSC7Palladium Stille Coupling
  254545. Enol Triflate
  254546. Organostannane
  254547. 21837N
  254548. 2/28/96V
  254549. Enantioselective Synthesis of Natural (-)-Austalide B, an Unusual Ortho Ester Metabolite Produced by Toxigenic Cultures of Aspergillus ustusW
  254550. 1994X
  254551. 2665Y
  254552. 116 (6)
  254553. Paquette, L. A.B
  254554. JACSC2Claisen Condensation
  254555. Potassium Enolate
  254556. Keto Ester
  254557. 21838N
  254558. 2/28/96V
  254559. Enantioselective Synthesis of Natural (-)-Austalide B, an Unusual Ortho Ester Metabolite Produced by Toxigenic Cultures of Aspergillus ustusW
  254560. 2665Y
  254561. 116 (6)
  254562. A    Padwa, A.B
  254563. JACSCfCyclopropane Synthesis
  254564. Rhodium Acetate
  254565. Samarium Iodide Deoxygenation
  254566. Reduction
  254567. Rhodium Carbene ComplexI
  254568. 21839N
  254569. 2/28/96V
  254570. Synthetic Studies toward Illudins and Ptaquilosin.  A Highly Convergent Approach via the Dipolar Cycloaddition of Carbonyl YlidesW
  254571. 1994X
  254572. 2667Y
  254573. 116 (6)
  254574. A    Ogawa, A.B
  254575. JOCC?Vinyl Tellurides
  254576. Cuprates
  254577. Lithium Tellurium Exchange
  254578. Carbanion
  254579. 21840N
  254580. 2/28/96VbHighly Regio- and Stereoselective Alkylation of vic-Bis(phenyltelluro)alkenes with Organocuprates W
  254581. 1994X
  254582. 1600Y
  254583. 59 (7)
  254584. A    Shono, T.B
  254585. JOCC"Annulation
  254586. Radical Anion
  254587. ReductionI
  254588. 21841N
  254589. 2/28/96V
  254590. Electroorganic Chemistry.  144.  Electroreductive Coupling of Ketones with O-Methyl Oximes, N,N-Dimethylhydrazones, and Nitrones.  A Convenient Route to Synthesis of b-Amino AlcoholW
  254591. 1994X
  254592. 1730Y
  254593. 59 (7)
  254594. Evans, D. A.B
  254595. JACSC4Aziridine
  254596. Silyl Enol Ether
  254597. a-Amino Ketone Synthesis
  254598. 21842N
  254599. 2/28/96
  254600. VBDevelopement of the Copper Catalyzed Olefin Aziridination ReactionW
  254601. 1994X
  254602. 2742Y
  254603. 116 (7)
  254604. Mikami, K.B
  254605. JACSCUChiral Organotitanium Catalyst
  254606. Hetero-Diels-Alder Reaction
  254607. Tetrahydropyran Synthesis
  254608. 21843N
  254609. 2/28/96V
  254610. Asymmetric Catalysis of Diels-Alder Cycloadditions by an MS-Free Binaphthol Titanium Complex:  Dramatic Effect of MS, Linear vs Positive Nonlinear Relationship, and Synthetic ApplicationsW
  254611. 1994X
  254612. 2812Y
  254613. 116 (7)
  254614. Smith, R. A. J.B
  254615. JACSI
  254616. 21844N
  254617. 2/28/96V
  254618. The Mechanism of Organocuprate 1,4-Addition Reactions with a,b-unsaturated Ketones:  Formation of Cuprate Enone Complexes with Lithium DimethylcuprateW
  254619. 1994X
  254620. 2902Y
  254621. 116 (7)
  254622. Wulff, W. D.B
  254623. JACSC]Chromium Carbonyl Complex
  254624. Organostannane
  254625. Annulation
  254626. Phenol Synthesis
  254627. Fischer Carbene Complex
  254628. 21845N
  254629. 2/28/96V\Contrasteric Regiochemical Incorporation of Stannylacetylenes in the Benzannulation ReactionW
  254630. 1994X
  254631. 3113Y
  254632. 116 (7)
  254633. Hoveyda, A. H.B
  254634. CdGrignard Reagent
  254635. Zirconium
  254636. Ruthenium Complex
  254637. Asymmetric Catalytic Carbomagnesation
  254638. Olefin MetathesisI
  254639. 21846N
  254640. 2/28/96V0Zirconium Catalyzed Kinetic Resolution of PyransW
  254641. 1994X
  254642. 3123Y
  254643. 116 (7)
  254644. Fukuyama, T.B
  254645. JACSC
  254646. Copper (II) Catalyzed Cyclopropane Prep
  254647. Bromination of Lithium Enolate
  254648. Intramolecular Cyclopropanation
  254649. Aldol Reaction
  254650. Cationic Cyclization
  254651. Annulation
  254652. Palladium Carbonylation
  254653. Indole Synthesis
  254654. Michael Addition of LiCH(SMe)(SOMe)
  254655. Curtius Reaction
  254656. 21847N
  254657. 2/28/96V/Stereocontrolled Synthesis of (-)-Hapalindole GW
  254658. 1994X
  254659. 3125Y
  254660. 116 (7)
  254661. Fukuyama, T.B
  254662. JACSC
  254663. Radical Ring Closure
  254664. Organostannane
  254665. Isonitrile
  254666. Palladium Stille Coupling
  254667. 2,3-Disubstituted Indole Synthesis
  254668. Imidoyl Radical
  254669. ORTHO ALKENYL ARYL ISONITRILE, TIN HYDRIDE, ALPHA STANNYLIMIDOYL RADICAL, IMIDOYL, CYCLIZATION TO INDOLE, STILLE COUPLINGI
  254670. 21848N
  254671. 2/28/96V%A Novel Tin Mediated Indole SynthesisW
  254672. 1994X
  254673. 3127Y
  254674. 116 (7)
  254675. Curran, D. P.B
  254676. CLRadical 
  254677. Cycloaddition
  254678. Organostannane
  254679. Chiral Auxillary
  254680. Diels-Alder Reaction
  254681. High Barrier to Bond RotationM
  254682. 21849N
  254683. 2/28/96VFAtroposelective Thermal Reactions of Axially Twisted Amides and ImidesW
  254684. 1994X
  254685. 3131Y
  254686. 116 (7)
  254687. Oppolzer, W.B
  254688. JACSCSRetro Cope Elimination Mechanism
  254689. Pictet Spengler Cyclization
  254690. Cuprate SN2' Reaction
  254691. K<Reaction proceeds stereospecifically in a suprafacial mannerM
  254692. 21850N
  254693. 2/28/96VpSuprafaciality of Thermal N-4-Alkenylhydroxylamine Cyclizations:  Synthesis of (
  254694. )-a-Lycorane and (+)-TrianthineW
  254695. 1994X
  254696. 3139Y
  254697. 116 (7)
  254698. Corey, E. J.B
  254699. JACSI
  254700. 21851N
  254701. 2/28/96V\Chemical Emulation of the Biosynthetic Route to Glycinoelepin from a Cycloartenol DerivativeW
  254702. 1994X
  254703. 3149Y
  254704. 116 (7)
  254705. Corey, E. J.B
  254706. JACSCLOrganostannane
  254707. Boron Chiral Promoter
  254708. Asymmetric Propargyl Alcohol Synthesis
  254709. 21852N
  254710. 2/28/96VUHighly Enantioselective Alkynylation of Aldehydes Promoted by Chiral OxazaborolidinesW
  254711. 1994X
  254712. 3151Y
  254713. 116 (7)
  254714. A    Jeong, N.B
  254715. JACSC4Cobalt Mediated Annulation
  254716. Cyclopentenone Synthesis
  254717. 21853N
  254718. 2/28/96V.Catayltic Version of the Pauson Khand ReactionW
  254719. 1994X
  254720. 3159Y
  254721. 116 (7)
  254722. Yamamoto, Y.B
  254723. JACSCOAmino ester Synthesis
  254724. Amino nitrile Synthesis
  254725. Rhodium Transition Metal CatalystI
  254726. 21854N
  254727. 2/28/96VETransition Metal Catalyzed Addition of Certain Nucleophiles to IminesW
  254728. 1994X
  254729. 3161Y
  254730. 116 (7)
  254731. Trost, B. M.B
  254732. JACSCbMichael Addition
  254733. Acetylene
  254734. a,b-Unsaturated Carbonyl Compound
  254735. Vinyl Triphenylphosphine IntermediateI
  254736. KP Nucleophilic g Addition to Acetylenes Bearing Electron Withdrawing SubstituentsM
  254737. 21855N
  254738. 2/28/96VGNovel "Umpolung" in C-C Bond Formation Catalyzed by Triphenyl PhosphineW
  254739. 1994X
  254740. 3167Y
  254741. 116 (7)
  254742. A    Kahne, D.B
  254743. JACSC?Enediyne Antibiotics
  254744. DNA Cleavage
  254745. Diradical
  254746. Bergman CyclizationI
  254747. 21856N
  254748. 2/28/96VeAnalysis of Hydroxylamine Glycoside Linkages:  Structural Consequenes of the NO Bond in CalicheamicinW
  254749. 1994X
  254750. 3197Y
  254751. 116 (8)
  254752. Beak, P.B
  254753. JACSC9Lithium Carbanion
  254754. Sparteine
  254755. trans-2,5-dimethylpyrrolidineI
  254756. 21857N
  254757. 2/28/96VwComplex Induced Proximity Effects:  Enantioselective Syntheses Based on Asymmetric Deprotonations of N-Boc-pyrrolidinesW
  254758. 1994X
  254759. 3231Y
  254760. 116 (8)
  254761. A    Adams, J.B
  254762. JACSC,Rhodium Carbene
  254763. Diazoketone
  254764. Rhodium Acetate
  254765. 21858N
  254766. 2/28/96VaModel Studies of the Stereoelectronic Effect in Rh(II) Mediated Carbenoid C-H Insertion ReactionsW
  254767. 1994X
  254768. 3296Y
  254769. 116 (8)
  254770. Paquette, L. A.B
  254771. JACSC Horner Emmons Wadsworth ReactionI
  254772. 21859N
  254773. 2/28/96V
  254774. Total Synthesis of the Cembranoid Diterpene Lactone (+)-Clemeolide.  Some Remarkable Conformational Features of Nine-Membered Belts Linked in 2,6-Fashion to a MethylenecyclohexaneW
  254775. 1994X
  254776. 3367Y
  254777. 116 (8)
  254778. Corey, E. J.B
  254779. JACSC1Boron Lewis Acid Catalyst
  254780. Tryptophan
  254781. Amino Acid 
  254782. 21860N
  254783. 2/28/96
  254784. Demonstration of the Synthetic Power of Oxazaborolidine Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberlic AcidW
  254785. 1994X
  254786. 3612Y
  254787. 116 (8)
  254788. Paterson, I.B
  254789. JACSC
  254790. Boron Enolate
  254791. Tin Enolate
  254792. 21861N
  254793. 2/28/96VrSubstrate Controlled Aldol Reaction of Chiral Ethyl Ketones:  Application oto the Total Synthesis of Oleandomycin W
  254794. 1994X
  254795. 3623Y
  254796. 116 (8)
  254797. A    Ojima, I.B
  254798. JACSC6Rhodium Catalyzed Carcosilation of Alkynes
  254799. Annulation
  254800. 21862N
  254801. 2/28/96VNExtremly Chemoselective Silylformylation and Silylcarbocyclization of AlkynalsW
  254802. 1994X
  254803. 3643Y
  254804. 116 (8)
  254805. Kita, Y.B
  254806. JACSC(Cation Radical Mechanism
  254807. Oxidation
  254808. AzideI
  254809. 56% yieldM
  254810. 21863N
  254811. 2/28/96V
  254812. Hypervalent Iodine Induced Nucleophilic Substitution of para-Substituted Phenol Ethers.  Generation of Cation Radicals as Reactive IntermediatesW
  254813. 1994X
  254814. 3684Y
  254815. 116 (9)
  254816. Nicolaou, K. C.B
  254817. C>Enedyne Antibiotics
  254818. DNA Cleavage
  254819. Diradical
  254820. Bergman CyclizationI
  254821. 21864N
  254822. 2/28/96V~Interaction of Calicheamicin with Duplex DNA:  Role of the Oligosaccharide Domain and Identification of Multiple Binding ModesW
  254823. 1994X
  254824. 3697Y
  254825. 116 (9)
  254826. Nicolaou, K. C.B
  254827. JACSC>Enedyne Antibiotics
  254828. DNA Cleavage
  254829. Diradical
  254830. Bergman CyclizationI
  254831. 21865N
  254832. 2/28/96VXCarbohydrate-Minor Groove Interactions in the Binding of Calicheamycin g1I to Duplex DNAW
  254833. 1994X
  254834. 3709Y
  254835. 116 (9)
  254836. A    Togni, A.B
  254837. JACSC'Chiral Ligand for Asymmetric Catalysis
  254838. KZ2. An Unusual, Selective h3-h1 Allyl Isomerization in a Chiral Allylic Alkylation CatalystM
  254839. 21866N
  254840. 2/28/96V
  254841. 1. A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration ReactionsW
  254842. 1994X
  254843. 4062, 4067Y
  254844. 116 (9)
  254845. Mikami, K.B
  254846. JACSC
  254847.  BINOL Titanium Lewis AcidI
  254848. 21867N
  254849. 2/28/96
  254850. VxAsymmetric Catalytic Aldol Type Reaction with Silyl Ketene Acetals:  Possible Intervention of the Silatropic Ene PathwayW
  254851. 1994X
  254852. 4077Y
  254853. 116 (9)
  254854. Hatakeyama, S.B
  254855. JACSC
  254856. Photochemistry
  254857. [2+2] photocycloaddition
  254858. Vinyl Carbanion
  254859. Allenylmethyl trimethylsilane
  254860. Phenyliodine(III)diacetate Radical OxidationI
  254861. 21868N
  254862. 2/28/96V#Total Synthesis of (-)-PaeoniflorinW
  254863. 1994X
  254864. 4081Y
  254865. 116 (9)
  254866. Kobayashi, S.B
  254867. JACSC
  254868. Ytterbium Chiral Lewis AcidI
  254869. 21869N
  254870. 2/28/96V
  254871. Lanthanide(III)-Catalyzed Enantioselective Diels-Alder Reactions.  Stereoselective Synthesis of Both Enantiomers by Using a Single Chiral Source and a Choice of Achiral Ligands W
  254872. 1994X
  254873. 4083Y
  254874. 116 (9)
  254875. Trost, B. M.B
  254876. JACSC'Palladium Catalyst Mediated Alkylation
  254877. 21870N
  254878. 2/28/96VFAsymmetric Induction in Allylic Alkylations of 3-(Acyloxy)cycloalkenesW
  254879. 1994X
  254880. 4089Y
  254881. 116 (9)
  254882. RajanBabu, T. V.B
  254883. JACSC-Asymmetric Hydrogenation
  254884. Carbohydrate LigandsI
  254885. 21871N
  254886. 2/28/96
  254887. Electronic Amplification of Selectivity in Rhodium Catalyzed Hydrogenation:  D-Glucose Derived Ligands for the Synthesis of D- or L-Amino Acids W
  254888. 1994X
  254889. 4101Y
  254890. 116 (9)
  254891. Yamamoto, H.B
  254892. JACSCMLewis Acid 
  254893. Michael Addition
  254894. Oganolithium
  254895. Organomagnesium
  254896. Silyl Ketene AcetalI
  254897. Conjugate Addition favoured over 1,2-addition due to shielding of the aldehyde carbonyl being located in a tight pocket of the ATPH complex M
  254898. 21872N
  254899. 2/28/96V{Virtually Complete Blocking of a,b-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide)W
  254900. 1994X
  254901. 4131Y
  254902. 116 (9)
  254903. Winkler, J. D.B
  254904. JACSC#Photochemistry
  254905. Retro Aldol ReactionI
  254906. 21873N
  254907. 2/28/96V
  254908. Inside-Outside Stereisomerization . 6.  Synthesis of trans-Bicyclo[4.4.1]undecan-11-one and the First Stereoselective Construction of the Tricyclic Nucleus of the Ring System of the Ingenane DiterpenesW
  254909. 1994X
  254910. 4183Y
  254911. 116 (10)
  254912. Hayashi, T. B
  254913. C9Palladium Asymmetric Silylation
  254914. Chiral Ruthenium CatalystI
  254915. 21874N
  254916. 2/28/96VxOptically Active Ruthenocenylbis(phosphines):  New Effieient Chiral Phosphine Ligands for Catalytic Asymmetric ReactionsW
  254917. 1994X
  254918. 4221Y
  254919. 116 (10)
  254920. Trost, B. M.B
  254921. JACSC
  254922. Diels-Alder
  254923. Diene SynthesisI
  254924. 21875N
  254925. 2/28/96VFPalladium Catalyzed Cycloisomerization to 1,2-DialkylidenecycloalkanesW
  254926. 1994X
  254927. 4255, 4268Y
  254928. 116 (10)
  254929. Curran, D. P.B
  254930. JACSC3Selenium Chemistry 
  254931. Atom Transfer Radical ChemistryI
  254932. 21876N
  254933. 2/28/96VFGroup Transfer Addition Reactions of Methyl(phenylseleno)malononitrileW
  254934. 1994X
  254935. 4279Y
  254936. 116 (10)
  254937. Dussault, P. H.B
  254938. JACSC*Radical Addition
  254939. Organostannane
  254940. Oxidation
  254941. 21877N
  254942. 2/28/96VmStereoselective Dioxygenation of Allylstannanes:  Synthesis of Enantiomerically Enriched Allyl HydroperoxidesW
  254943. 1994X
  254944. 4485Y
  254945. 116 (10)
  254946. Martin, S. F.B
  254947. JACSC
  254948. Rhodium Carbene Complex
  254949. 21878N
  254950. 2/28/96
  254951. VkEnantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic DiazoacetatesW
  254952. 1994X
  254953. 4493Y
  254954. 116 (10)
  254955. Magnus, P.B
  254956. JACSC%Azide Synthesis
  254957. Oxidation
  254958. Lewis Acid
  254959. 21879N
  254960. 2/28/96V
  254961. a-Azidonation of Amides, Carbamates, and Ureas with the Iodosylbenzene/ Trimethylsilyl Azide Reagent Combination: N-Acyliminium Ion PrecursorsW
  254962. 1994X
  254963. 4501Y
  254964. 116 (10)
  254965. Doyle, M. P.B
  254966. JACSCeRhodium Carbebe Complex
  254967. Diazoester
  254968. Chiral Dirhodium (II) Carboxamide Catalyst
  254969. C-H Insertion Reaction
  254970. 21880N
  254971. 2/28/96VlDiastereocontrol for Highly Enantioselective Carbon-Hydrogen Insertion Reactions of Cycloalkyl DiazoacetatesW
  254972. 1994X
  254973. 4507Y
  254974. 116 (10)
  254975. Johnson, C. R. B
  254976. Silyl Enol Ether
  254977. Reduction
  254978. 21881N
  254979. 2/28/96V
  254980. Hydrosilylation of Enones:  Platinum Divinyltetramethyldisiloxane Complex in the Preparation of Triisopropylsilyl and Triphenylsilyl Enol EthersW
  254981. 1994X
  254982. 2287Y
  254983. 59 (9)
  254984. Brown, H. C.B
  254985. Aldol Chemistry
  254986. Boron EnolateI
  254987. 21882N
  254988. 2/28/96V
  254989. Enolboration. 6.  Dicyclohexyliodoborane, a Versitile Reagent for the Stereoselective Synthesis of Either Z or E Enolates from Representative Esters W
  254990. 1994X
  254991. 2336Y
  254992. 59 (9)
  254993. Brown, H. C.B
  254994. 21883N
  254995. 2/28/96
  254996. SHydroboration.  91.  Improved Procedure for the Synthesis of Optically Pure Bis-Adducts, N,N,N',N'-Tetramethyletylenediamine
  254997. 2-organylapiosopinocampheylboranes, from the Corresponding 2-Organylapopinenes of Lower Optical Purity.  Conversion of These Adducts into 2-Organylapoisopinocampheylboranes, Useful Asymmetric Hydroboraing Reagents 
  254998. 1994X
  254999. 2365Y
  255000. 59 (9)
  255001. Meyers, A. I.B
  255002. JOCCLAsymmetric Ullmann Coupling
  255003. Chiral Biaryl Synthesis
  255004. Copper Mediated CouplingI
  255005. 21884N
  255006. 2/28/96V*A Rapid Total Synthesis of an EllagitanninW
  255007. 1994X
  255008. 2577, 2655Y
  255009. 59 (9)
  255010. ISHIKURA, M.
  255011. JOCCDPalladium Coupling
  255012. Boron Ate Complex
  255013. Indole Synthesis
  255014. Carbonylation
  255015. 21885N
  255016. 2/28/96
  255017. Palladium Catalyzed Carbonylative Cross Coupling Reactions with Triethyl(1-methylindol-2-yl)borate:  A Simple Route to 1-Methylindol-2-yl KetonesW
  255018. 1994X
  255019. 2634Y
  255020. 59 (9)
  255021. Rychnovsky, S. D.B
  255022. Acetylene to AlkeneI
  255023. 21886N
  255024. 2/28/96V`Triphenylphosphine Catalyzed Isomerizations of Enynes to (E,E,E) tienes:  Phenol as a CocatalystW
  255025. 1994X
  255026. 2659Y
  255027. 59 (9)
  255028. Shibasaki, M.B
  255029. JOCC,Nitroaldol
  255030. Cyanosilylation
  255031. Lanthanide Bases
  255032. 21887N
  255033. 2/28/96V
  255034. Catalytic Aldol Reactions with Sm(HMDS)3 and its Application for the Introduction of a Carbon-Carbon Triple Bond at C-13 in Prostaglandin SynthesisW
  255035. 1994X
  255036. 2661Y
  255037. 59 (9)
  255038. Martin, S. F.B
  255039. JACSC
  255040. Asymmetric Aldol Reaction
  255041. Oxidation of Furan Ring
  255042. Stereoselective Cuprate Addition
  255043. Lewis Acid Addition of Crotyl Stannane
  255044. Stereoselective Reduction of KetoneI
  255045. 21888N
  255046. 2/28/96VhStategies for Macrolide Synthesis.  A Concise Approach to Protected Seco-Acids of Erythronolides A and BW
  255047. 1994X
  255048. 4674Y
  255049. 116 (11)
  255050. Paquette, L. A. B
  255051. JACSC}Double Michael Addition Ring Annulation
  255052. Conjugate Addition
  255053. Lithio(TMS)acetonitrile
  255054. Radical Deoxygenation of a SelenocarbonateI
  255055. 21889N
  255056. 2/28/96VuTotal Synthesis of the Lycopodium Alkaloids Magellanine and Magellaninone by Threefold Annulation of 2-CyclopentenoneW
  255057. 1994X
  255058. 4689Y
  255059. 116 (11)
  255060. Meyers, A. G. B
  255061. JACSCXTriethyl Boron Initiated Radical Cyclization
  255062. Carbohydrate Chemistry
  255063. Glycoside Coupling
  255064. 21890N
  255065. 2/28/96V
  255066. Synthetic Studies on the Tunicamycin Antibiotics.  Preparation of (+)-Tunicaminyluracil, (+)-Tunicamycin-V, and 5'-epi-Tunicamycin-VW
  255067. 1994X
  255068. 4697Y
  255069. 116 (11)
  255070. Comins, D. L.B
  255071. JACSC)Chiral Pyridinium Salts
  255072. Dihydropyridones
  255073. 21891N
  255074. 2/28/96V
  255075. Asymmetric Synthesis of 2-Alkyl(Aryl)-2,3-dihydro-4-pyridones by Addition of Grignard Reagents to Chiral 1-Acyl-4-methoxypyridinium SaltsW
  255076. 1994X
  255077. 4719Y
  255078. 116 (11)
  255079. Frenking, G.B
  255080. C]Asymmetric Osmylation
  255081. Osmium Tetroxide
  255082. Diol Synthesis
  255083. Oxidation of Alkenes
  255084. Cinchona AlkaloidsI
  255085. 21892N
  255086. 2/28/96VcMechanism of the Enantioselective Dihyroxylation of Olefins by OsO4 in the Presence of Chiral BasesW
  255087. 1994X
  255088. 4937Y
  255089. 116 (11)
  255090. Jimenez, L. S.B
  255091. JACSCGDNA Alkylation
  255092. Annulation
  255093. Michael Addition
  255094. Epoxide Synthesis
  255095. Aziridine
  255096. 21893N
  255097. 2/28/96VQSynthesis of the Tetracyclic Mitomycin Skeleton via a Dialkylvinyl Sulfonium SaltW
  255098. 1994X
  255099. 4977Y
  255100. 116 (11)
  255101. Majetich, G.B
  255102. JACSCELewis Acid Catalyzed Cycloalkylation
  255103. Carbocation Mediated Annulation
  255104. 21894N
  255105. 2/28/96V#Concise Synthesis of (
  255106. )-PerovskoneW
  255107. 1994X
  255108. 4979Y
  255109. 116 (11)
  255110. Majetich, G.B
  255111. JACSC3Europium Catalyzed Diels-Alder Reaction
  255112. Lewis Acid
  255113. 21895N
  255114. 2/28/96V#Concise Synthesis of (
  255115. )-PerovskoneW
  255116. 1994X
  255117. 4979Y
  255118. 116 (11)
  255119. Trost, B. M.B
  255120. JACSC@Terminal Olefins
  255121. Acetylene
  255122. Transition Metal Mediated Annulation
  255123. Terminal olefins only
  255124. 21896N
  255125. 2/28/96
  255126. Buteneolide Synthesis Based Upon a Contra-Electronic Addition in a Ruthenium Catalyzed Alder Ene Reaction.  Synthesis and Absolute Configuration of (+)-AncepsenolideW
  255127. 1994X
  255128. 4985Y
  255129. 116 (11)
  255130. A    Kishi, Y.B
  255131. JACSI
  255132. 21897N
  255133. 2/28/96V5Novel Structure Elucidation of AAL Toxin TA Backbone
  255134. 1994X
  255135. 4995Y
  255136. 116 (11)
  255137. Boger, D. L.B
  255138. JACSI
  255139. 21898N
  255140. 2/28/96V
  255141. Total Synthesis of Bleomycin and Related Agents.  1. Synthesis and DNA Binding Properties of the Extended C-Terminus:  Tripeptide S, Tetrapeptide S, Pentapeptide S, and Related AgentsW
  255142. 1994X
  255143. 5607, 5619, 5631, Y
  255144. 116 (13)
  255145. Hartwig, J. F.B
  255146. JACSC!Organostannane
  255147. Aniline Synthesis
  255148. 21899N
  255149. 2/28/96V
  255150. Palladium Catalyzed Formation of Carbon-Nitrogen Bonds.  Reaction Intermediates and Catalyst Improvements in the Hetero Cross-Coulping of Aryl Halides and Tin AmidesW
  255151. 1994X
  255152. 5969Y
  255153. 116 (13)
  255154. Buchwald, S. F.B
  255155. JACSC;Optically Active Amine
  255156. Chiral Titanium Catalyst
  255157. Reduction
  255158. 21900N
  255159. 2/28/96VFAsymmetric Hydrogenation of Enamines with a Chiral Titanocene CatalystW
  255160. 1994X
  255161. 5985Y
  255162. 116 (13)
  255163. Fuchs, P. L.B
  255164. JACSC
  255165. Sulfone Carbanion
  255166. 21901N
  255167. 2/28/96V
  255168. A Highly Efficient Synthesis of b-Substituted Six- and Seven -Membered-Ring Enones via Carbon Alkylation of g-Methoxy  Allylsulfonyl AnionsW
  255169. 1994X
  255170. 5995Y
  255171. 116 (13)
  255172. Collum, D. B.B
  255173. JACSC
  255174. Li nmr
  255175. Carbanion
  255176. 21902N
  255177. 2/28/96VpStructure of Lithium Hexamethyldisilazide:  Spectroscopic Study of Ethereal Solvation in the Slow Exchange LimitW
  255178. 1994X
  255179. 6009Y
  255180. 116 (13)
  255181. Yamamoto, Y.B
  255182. JACSI
  255183. 21903N
  255184. 2/28/96VTPalladium Catalyzed Addition of Activated Methylene and Methyne Compounds to AllenesW
  255185. 1994X
  255186. 6019Y
  255187. 116 (13)
  255188. A    Murai, S.B
  255189. JACSCBAnnulation
  255190. Ruthenium Complex Catalyzed Cyclization
  255191. Diene SynthesisI
  255192. 21904N
  255193. 2/28/96VsHighly Selective Skeletal Reorganization of 1,6- and 1,7-Enynes to 1-Vinyl Cycloalkenes Catalyzed by  [RuCl2(CO)3]2W
  255194. 1994X
  255195. 116 (13)
  255196. Yamamoto, H.B
  255197. JACSC?Conjugate Addition
  255198. Carboxylation
  255199. Addition to Aldehyde or KetoneI
  255200. 21905N
  255201. 2/28/96VjAllylbarium Reagents:  Unprecedented Regio- and Stereoselective Allylation Reactions of Carbonyl CompoundsW
  255202. 1994X
  255203. 6130Y
  255204. 116 (14)
  255205. Yamamoto, H.B
  255206. JACSC
  255207. Lewis Acid
  255208. 21906N
  255209. 2/28/96V
  255210. Asymmetric Diels-Alder Reaction of Unsymetrical Maleates.  A Chemical Access to Chiral, Unsymetrical cis-Cyclohexene-1,2-dicarboxylatesW
  255211. 1994X
  255212. 6153Y
  255213. 116 (14)
  255214. Stille, J. R.B
  255215. JACSC+Annulation
  255216. Enamine
  255217. Imine
  255218. Michael Addition 
  255219. 21907N
  255220. 2/28/96VvAsymmetric Formation of Quaternary Centres through Aza-Annulation of Chiral b-Enamino Esters with Acrylate DerivativesW
  255221. 1994X
  255222. 6201Y
  255223. 116 (14)
  255224. Meyers, A. I.B
  255225. JACSC#Chiral Oxazoline
  255226. Conjugate AdditionI
  255227. 21908N
  255228. 2/28/96VeAsymmetric Michael Type Addition of Lithium Amides to Aromatic Systems Leading to Novel b-Amino acidsW
  255229. 1994X
  255230. 6437Y
  255231. 116 (14)
  255232. Wulff, W. D.
  255233. JACSC.Annulation
  255234. Phenol Synthesis
  255235. CycloaromatizationI
  255236. 21909N
  255237. 2/28/96V[First Stereoselective Synthesis of Arene Chromium Complexes via the Benzannulation ReactionW
  255238. 1994X
  255239. 6449Y
  255240. 116 (14)
  255241. Nishida, M.B
  255242. JACSC4Radical Cyclization
  255243. Organnostannane
  255244. Chiral AuxiliaryI
  255245. 21910N
  255246. 2/28/96V^Lewis Acid Promoted Diastereoselective Radical Cyclization Using Chiral a,b-unsaturated EstersW
  255247. 1994X
  255248. 6455Y
  255249. 116 (14)
  255250. Roush, W. R.B
  255251. JACSC
  255252. Intramolecular Diels-Alder
  255253. Asymmetric Borane Reduction
  255254. Palladium Suzuki Coupling
  255255. Horner Emmons Olefination
  255256. BOP-Cl promoted Macrolactonization
  255257. LiHMDS Dieckmann CyclizationI
  255258. 21911N
  255259. 2/28/96V9Enantioselective Total Synthesis of  (-)-ChlorothricolideW
  255260. 1994X
  255261. 6457Y
  255262. 116 (14)
  255263. Boger, D. L.B
  255264. JACSC%DNA Alkylation
  255265. Antitumor Antibiotics
  255266. 21912N
  255267. 2/28/96
  255268. Chemical and Structural Comparison of N-BOC-CBQ and N-BOC-CBI:  Identification and Structural Orgin of an Unappreciated but Productive Stability of the CC-1065 and Duocarmycin SA Alkylation SubunitsW
  255269. 1994X
  255270. 6461Y
  255271. 166 (14)
  255272. Schreiber, S. L.B
  255273. SynlettC
  255274. FK506
  255275. RapamycinI
  255276. 21913N
  255277. 2/28/96V;Synthesis, Structure and Mechanism in Immunophilin ResearchW
  255278. 1994X
  255279. no. 6
  255280. Burgess, K.B
  255281. JACSC)Transition Metal Catalyzed Hydroboration
  255282. 21914N
  255283. 2/28/96V5Titanium Mediated Additions of Borohydride to AlkenesW
  255284. 1994X
  255285. 6561Y
  255286. 116 (15)
  255287. Jacobsen, E. J.B
  255288. JACSC+Manganese Salen Complex
  255289. Cinchonda AlkaloidsI
  255290. 21915N
  255291. 2/28/96V
  255292. Effect of Chiral Quaternary Ammonium Salts on (salen)-Mn-Catalyzed Epoxidation of cis-Olefins.   A Highly Enantioselective, Catalytic Route to Trans EpoxidesW
  255293. 1994X
  255294. 6937Y
  255295. 116 (15)
  255296. Hart, D. J.B
  255297. JACSC?Radical Cyclization
  255298. Reduction Triethylsilane
  255299. Tebbe Olefination
  255300. 21916N
  255301. 2/28/96
  255302.  V%Total Synthesis of dl-21-OxogelsemineW
  255303. 1994X
  255304. 6943Y
  255305. 116 (15)
  255306. Barluenga, J. B
  255307. JACSC%Chromium Complex
  255308. Chiral D-A Reaction
  255309. 21917N
  255310. 2/28/96V
  255311. Asymmetric Exo-Selective Diels-Alder Reaction of Cyclic BF2 Adducts of Functionalized Fischer Vinylcarbene Complexes with Chiral 2-Amino-1,3-dienes W
  255312. 1994X
  255313. 6949Y
  255314. 116 (15)
  255315. Kahne, D. B
  255316. JACSC;Glycoside
  255317. Solid Phase Carbohydrate Synthesis
  255318. OligosaccarideI
  255319. 21918N
  255320. 2/28/96V?Glycosylation on the Merrifield Resin Using Anomeric SulfoxidesW
  255321. 1994X
  255322. 6953Y
  255323. 116 (15)
  255324. Canary, J. W.B
  255325. JACSC-Palladium Catalyzed Coupling of Bornic Acids
  255326. 21919N
  255327. 2/28/96V_Observation of Catalytic Intermediates in the Suzuki Reaction by Electrospray Mass SpectrometryW
  255328. 1994X
  255329. 6985Y
  255330. 116 (15)
  255331. Denmark, S. E.B
  255332. JACSCSLewis Acid Catalyzed Aldol Reaction
  255333. Mukaiyama Aldol
  255334. Silicon
  255335. Hydroxy Ester SynthesisI
  255336. 21920N
  255337. 2/28/96VQChemistry of Enoxysilacyclobutanes:  Highly Selective Uncatalyzed Aldol AdditionsW
  255338. 7026Y
  255339. 116 (16)
  255340. Semmelhack, M. F.
  255341. Wulff, W. D.B
  255342. JACSC
  255343. Mo Complexes
  255344. Annulation
  255345. 21921N
  255346. 2/28/96V
  255347. Metal Catalyzed Cyclopropene Rearrangements for Benzoannulation:  Evaluation of an Anthraquinone Synthesis Pathway and Reevaluation of the Parallel Approach via Carbene Chromium ComplexesW
  255348. 1994X
  255349. 7108Y
  255350. 116 (16)
  255351. Yamada, K.B
  255352. JACSC
  255353. Evans Syn Aldol Reaction
  255354. Sharpless Epoxidation
  255355. Horner-Emmons
  255356. Julia Coupling
  255357. Macrolactonization (Yamaguchi method)
  255358. Sulfone Li Carbanion 
  255359. AlkylationI
  255360. 21922N
  255361. 2/28/96V
  255362. 1. Absolute Stereochemistry of Aplyronine A, a Potent Antitumor Substance of Marine Orgin 
  255363. 2. Total Synthesis of Aplyronine A, a Potent Antitumor Substance of Marine Orgin W
  255364. 1994X    7441,7443Y
  255365. 116 (16)
  255366. Fallis, A. G.B
  255367. JACSC
  255368. Annulation
  255369. K*Also see A. Fallis JOC 1994, 59 (22), 6514M
  255370. 21923N
  255371. 2/28/96VOSamarium(II) Iodide Induced Radical Cyclization of Halo- and CarbonylhydrazonesW
  255372. 1994X
  255373. 7447Y
  255374. 116 (16)
  255375. Wulff, W. D.B
  255376. (C,Organnostannane
  255377. Annulation
  255378. Chromium Complex
  255379. 21924N
  255380. 2/28/96VSPalladium Catalyzed Cross Coupling of Arene-Chromium Tricarbonyl Triflate ComplexesW
  255381. 1994X
  255382. 7449Y
  255383. 116 (16)
  255384. Semmelhack, M. F.B
  255385. JACSC
  255386. Palladium Catalyzed Cyclization
  255387. Palladium Hydrostannylation
  255388. Claisen Rearrangement
  255389. Radical Deoxygenation
  255390. Corey Oxazaborolidine Chiral ReductionI
  255391. 21925N
  255392. 2/28/96V
  255393. Palladium Promoted Synthesis of Ionophore Antibiotics.  Strategy and Assembly of the Homochiral Tetrahydrofuran and Tetrahydropyran Portions of TetronomycinW
  255394. 1994X
  255395. 7455Y
  255396. 116 (16)
  255397. Trost, B. M.B
  255398. JACSCDRamberg Blacklund Reaction
  255399. Ruthenium Catalyzed Butenolide AnnulationI
  255400. 21926N
  255401. 2/28/96VIA Concise Convergent Synthesis to Acetogenins.  (+)-Solamin and AnologuesW
  255402. 1994X
  255403. 7459Y
  255404. 116 (16)
  255405. +A    Knapp, S.B
  255406. JACSC7Thiourea
  255407. Mercuric Oxide Mediated Cyclization
  255408.  OxazolineI
  255409. 21927N
  255410. 2/28/96VEA (1 - 4) "Trehazoloid Glucosidase Inhibitor with Aglycon SelectivityW
  255411. 1994X
  255412. 7461Y
  255413. 116 (16)
  255414. Grieco, P. A.B
  255415. JACSC8Copper (II) Mediated Ring Contraction
  255416. Lactone Synthesis
  255417. 21928N
  255418. 2/28/96V3C19 Quassinoids:  Total Synthesis of dl-Samaderin BW
  255419. 1994X
  255420. 7606Y
  255421. 116 (17)
  255422. Wulff, W. D.B
  255423. JACSC$Tungsten Carbene Cpmlex
  255424. Diels-Alder
  255425. 21929N
  255426. 2/28/96VyThree Component Intramolecular Two Alkyne Annulations of Fischer Carbene Complexes:  New Strategies for Steroid SynthesisW
  255427. 1994X
  255428. 7616Y
  255429. 116 (17)
  255430. Buchwald, S. L.B
  255431. JACSC
  255432. Organotin
  255433. Anilines
  255434. Arylamine
  255435. LiCl deactivates the reaction (product formed in the synthesis of the aminostannane).  The aminostannane was formed by reaction of N,N-diethylaminotributylstannane and the appropriate aniline with removal of the diethylamine.M
  255436. 21930N
  255437. 2/28/96VMPalladium Catalyzed Aromatic Aminations with in Situ Generated AminostannanesW
  255438. 1994X
  255439. 7901Y
  255440. 116 (17)
  255441. Sammakia, T.B
  255442. JACSC
  255443. Organotin 
  255444. Silyl Enol EtherI
  255445. 21931N
  255446. 2/28/96
  255447. /VaEvidence for an Oxocarbenium Ion Intermediate in Lewis Acid Mediated Reactions of Acyclic AcetalsW
  255448. 1994X
  255449. 7915Y
  255450. 116 (17)
  255451. Takahashi, T.B
  255452. JACSC/Carbohydrate
  255453. Gylcoside Synthesis
  255454. OligosaccarideI
  255455. 21932N
  255456. 2/28/96VWSynthesis of An Elicitor-Active Analogue by a One-Pot, Two Step Glycosidation ProcedureW
  255457. 1994X
  255458. 7919Y
  255459. 116 (17)
  255460. Negishi, E-I.B
  255461. JACSC@Heck Cyclization
  255462. Annulation
  255463. Acylpalladium
  255464. Vinyl Iodide
  255465. palladiumI
  255466. 21933N
  255467. 2/28/96VnDeferred Carbonylative Esterification in the Palladium Catalyzed Cyclic Carbometallation-Carbonylation CascadeW
  255468. 1994X
  255469. 7923Y
  255470. 116 (17)
  255471. Collum, D. B.B
  255472. JACSC*Organolithium
  255473. Aggregation of Lithium AmideI
  255474. 21934N
  255475. 2/28/96VuStructure of LTMP and LPMP in Hydrocarbon Solution :  Assignment of Cyclic Trimer and Tetramer Conformational IsomersW
  255476. 1994X
  255477. 7949Y
  255478. 116 (17)
  255479. Boger, D. L.B
  255480. JACSC
  255481. DNA Alkylation 
  255482. 21935N
  255483. 2/28/96
  255484. CBI-TMI: Synthesis and Evaluation of a Key Analog of the Duocarmycins.  Validation of a Direct Relationship between Chemical Solvolytic Stability and Cytotoxic Potency and Conformation of the Structural Features Responsible for the Distinguishing Behavior of Enantiomeric Pairs of Agents
  255485. 1994X
  255486. 7996Y
  255487. 116 (18)
  255488. Hegedus, L. S.B
  255489. JACSC=Palladium Catalyzed Carbonylation
  255490. Organotin
  255491. Cuprate Addition
  255492. 21936N
  255493. 2/28/96V
  255494. Asymmetric Synthesis of a-Amino Acids by Copper Catalyzed Conjugate Addition of Grignard Reagents to Optically Active Carbamatoacrylates W
  255495. 1994X
  255496. 8126Y
  255497. 116 (18)
  255498. Nicolaou, K. C.B
  255499. JACSC%Carbanion
  255500. Aryl Lithium Rearrangement
  255501. 21937N
  255502. 2/28/96V
  255503. Total Synthesis of BalanolW
  255504. 1994X
  255505. 8402Y
  255506. 116 (18)
  255507. Negishi, E-I.B
  255508. JACSC"Annulation
  255509. Organoaluminum Reagent
  255510. 21938N
  255511. 2/28/96VATitanium Catalyzed Cascade Carboalumination of Dienes and TrienesW
  255512. 1994X
  255513. 8404Y
  255514. 116 (18)
  255515. West, F. G.B
  255516. 7C9Diazoketone
  255517. Stevens Rearrangement
  255518. Copper/ Rhodium CarbeneI
  255519. 21939N
  255520. 2/28/96VuPiperidines via Ammonium Ylide [1,2]-Shifts:  A Concise, Enantioselective Route to (-)-Epilupinine from Proline EsterW
  255521. 1994X
  255522. 8420Y
  255523. 116 (18)
  255524. Curran, D. P.B
  255525. JACSC)Radical Cyclization
  255526. Annulation
  255527. Organotin
  255528. 21940N
  255529. 2/28/96V
  255530. Substrate Controlled Group Selective Radical Cyclizations.  A New Strategy for Stereocontolled Transformations of Diastereomeric Reactive IntermediatesW
  255531. 1994X
  255532. 8430Y    116 (18) 
  255533. Sharpless, K. B.B
  255534. JACSC
  255535. Osmium Tetroxide
  255536. Oxidation
  255537. 21941N
  255538. 2/28/96V
  255539. Toward an Understanding of the High Enantioselectivity in the Osmium-Catalyzed Asymmetric Dihydroxylation. 2. A Qualitative Molecular Mechanics ApproachW
  255540. 1994X
  255541. 8470Y
  255542. 116 (19)
  255543. Quallich, G. J.B
  255544. JACSC
  255545. Enantioselective ReductionI
  255546. 21942N
  255547. 2/28/96VrA Comined Synthetic and ab Initio Study of Chiral Oxazaborolidines Structure and Enantioselectivity Relationships.W
  255548. 1994X
  255549. 8516Y
  255550. 116 (19)
  255551. Lautens, M.B
  255552. JACSC!Samarium
  255553. Organotin
  255554. Organosilicon
  255555. 21943N
  255556. 2/28/96V>Studies in the Directed Cyclopropanation of a-Allenic AlcoholsW
  255557. 1994X
  255558. 8526Y
  255559. 116 (19)
  255560. Roush, W. R.B
  255561. JACSC3Organnotin
  255562. Lewis Acid
  255563. Homoallylic Alcohol SynthesisI
  255564. 21944N
  255565. 2/28/96V
  255566. [(Z)-g-{Diisopropyllidene-a-D-mannopyranosyl)oxy]allyl]tributylstannane:  A New Chiral Reagent for the Asymmetric a-Hydroxyallylation of AldehydesW
  255567. 1994X
  255568. 8536Y
  255569. 116 (19)
  255570. Boger, D. L.B
  255571. JACSCHUllmann Aryl Ether Synthesis
  255572. Copper
  255573. Macrocyclization via amide formationI
  255574. 21945N
  255575. 2/28/96VSTotal Synthesis of Bouvardin, O-Methylbouvardin, and O-Methyl-N9-desmethylbouverdinW
  255576. 1994X
  255577. 8544Y
  255578. 116 (19)
  255579. Buchwald, S. L.B
  255580. JACSC@Annulation
  255581. Organotitanium 
  255582. Cyclopentenone Synthesis
  255583. Pauson KhandI
  255584. 21946N
  255585. 2/28/96VWDevelopement of a Titanocene Catalyzed Enyne Cyclization/ Isocyanide Insertion ReactionW
  255586. 1994X
  255587. 8593Y
  255588. 116 (19)
  255589. Chung, Y. K. B
  255590. ?C>Annulation
  255591. Organocobalt 
  255592. Cyclopentenone Synthesis
  255593. Pauson KhandI
  255594. 21947N
  255595. 2/28/96Vc(Indenyl)cobalt(I) Catalyzed Cocyclization of Alkyne, Alkene and Carbon Monoxide to CyclopentenonesW
  255596. 1994X
  255597. 8793Y
  255598. 116 (19)
  255599. Coleman, R. S.B
  255600. JACSC!Diels-Alder
  255601. Naphthalene SynthesisI
  255602. 21948N
  255603. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  255604. 1994X
  255605. 8795Y
  255606. 116 (19)
  255607. Coleman, R. S.B
  255608. JACSCABiaryl Cyanocuprate
  255609. Organocopper
  255610. Organolithium
  255611. Oxidative CouplingI
  255612. 21949N
  255613. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  255614. 1994X
  255615. 8795Y
  255616. 116 (19)
  255617. Coleman, R. S.B
  255618. JACSC*MnO2 Oxidative Phenoxy Radical CyclizationI
  255619. 21950N
  255620. 2/28/96VfAtropdiastereoselective Total Synthesis of Phleichrome and the Protein Kinase C Inhibitor Calphostin AW
  255621. 1994X
  255622. 8795Y
  255623. 116 (19)
  255624. Denmark, S. E.B
  255625. CCLChiral Aniline Synthesis
  255626. Organolithium
  255627. Chiral Ligand
  255628. Bis-Oxazoline
  255629. SparteineI
  255630. 21951N
  255631. 2/28/96V7Asymmetric Addition of Organolithium Reagents to IminesW
  255632. 1994X
  255633. 8797Y
  255634. 116 (19)
  255635. Townsend, C. A.B
  255636. JACSC
  255637. Enediyne AntibioticsI
  255638. 21952N
  255639. 2/28/96VbKinetic vs Thermodynamic Determinants in the Sequence Selectivity of DNA Cleavage by CalicheamicinW
  255640. 1994X
  255641. 8819Y
  255642. 116 (19)
  255643. Lautens, M. B
  255644. JACSCONickel Cyclooctadiene
  255645. Palladium Catalyzed Intramolecular Cyclization
  255646. AnnulationI
  255647. K+also see JACS 1994, 116, 8526 (this issue)
  255648. 21953N
  255649. 2/28/96VXStereochemical Control in Metal Catalyzed [3+2] Cycloadditions of MethylenecyclopropanesW
  255650. 1994X
  255651. 8821Y
  255652. 166 (19)
  255653. Koga, K.B
  255654. JACSC$Asymmetric Alkylation
  255655. Organolithium
  255656. 21954N
  255657. 2/28/96V
  255658. Catalytic Asymmetric Benzylation of Achiral Lithium Enolates Using a Chiral Ligand for Lithium in the Presence of a Achiral Ligand W
  255659. 1994X
  255660. 8829Y
  255661. 116 (19)
  255662. Carreira, E. M.B
  255663. GCQAsymmetric Mukaiyama Aldol Reaction
  255664. Chiral Titanium Catalyst
  255665. Silyl Ketene AcetalsI
  255666. 21955N
  255667. 2/28/96V
  255668. Catalytic, Enantioselective Aldol Additions with Methyl and Ethyl Acetate O-Silyl Enolates:  A Chiral Tridentate Chelate as a Ligand for Titanium (IV)W
  255669. 1994X
  255670. 8837Y
  255671. 116 (19)
  255672. HA    Luh, T-Y.B
  255673. JACSC*Dithioacetal
  255674. Dithioketal
  255675. Olefin Synthesis
  255676. 21956N
  255677. 2/28/96VdChelation Assistance in the Activation of Csp3-S Bonds in Nickel-Catalyzed Cross-Coupling Reactions W
  255678. 1994X
  255679. 8920Y
  255680. 116 (20)
  255681. Buchwald, S. L.B
  255682. JACSC7Organotitanium Hyride Reduction
  255683. Chiral Amine Synthesis
  255684. 21957N
  255685. 2/28/96V
  255686. 1. Catalytic Asymmetric Hydrogenation of Imines with a Chiral Titanocene Catalyst:  Scope and Limitations
  255687. 2. Kinetic Resolution of Racemic Disubstituted 1-Pyrrolines via Asymmetric Reduction  with a Chiral Titanocene CatalystW
  255688. 1994X
  255689. 8952, 9373Y
  255690. 116 (20)
  255691. Pirrung, M. C.B
  255692. JACSC3Organorhodium 
  255693. Rh catalyzed C-H Insertion ReactionsI
  255694. 21958N
  255695. 2/28/96
  255696. Electronic Effects in Dirhodium (II) Carboxylates.  Linear Free Energy Relationships in Catalyzed Decompositions of Diazo Compounds and CO and Isonitrile ComplexationW
  255697. 1994X
  255698. 8991Y
  255699. 116 (20)
  255700. Aube, J.B
  255701. JACSChPhotochemical Oxaziridine Rearrangement
  255702. Lactam Synthesis
  255703. Photochemistry
  255704. Bischler-Napieralski CyclizationI
  255705. 21959N
  255706. 2/28/96V
  255707. Symmetry-Driven Synthesis of Indole Alkaloids:  Asymmetric Total Synthesis of (+)-Yohimbine, (-)-Yohimbone, (-)-Yohimane, and (+)-Alloyohimbane W
  255708. 1994X
  255709. 9009Y
  255710. 116 (20)
  255711. Collum, D. B.B
  255712. JACSC$Li-6 NMR
  255713. N-15 NMR
  255714. LTMP StructureI
  255715. 21960N
  255716. 2/28/96V
  255717. 1. Lithium Dialkylamide Mixed Aggregation:  MNDO Comutational Study of Salt and Solvent Dependencies
  255718. 2. Lithium Dialkylamide Mixed Aggregation:  An NMR Spectroscopic Study of Hexamethylphosphoramide (HMPA)W
  255719. 1994X
  255720. 9187, 9198Y
  255721. 116 (20)
  255722. Jacobsen, E. N.B
  255723. JACSC;Epoxide Synthesis
  255724. Chiral Organomanganese Catalyst
  255725. OxidationI
  255726. 21961N
  255727. 2/28/96
  255728. MV?Highly Enantioselective, Low Temperature Epoxidation of StyreneW
  255729. 1994X
  255730. 9333Y
  255731. 116 (20)
  255732. Corey, E. J.B
  255733. JACSC
  255734. Organotitanium
  255735. Grigard Reagent
  255736. 21962N
  255737. 2/28/96V
  255738. Catalytic Diastereoselective Synthesis of Cis-1,2-Disubstituted Cyclopropanols from Esters Using a Vicinal Dicarbanion EquivalentW
  255739. 1994X
  255740. 9345Y
  255741. 116 (20)
  255742. Meyers, A. G.B
  255743. JACSC5Enantioselective Alkylation
  255744. Reduction
  255745. Lithium EnolateI
  255746. 21963N
  255747. 2/28/96VMUse of Pseudoephedine as a Practical Chiral Auxilary for Asymmetric SynthesisW
  255748. 1994X
  255749. 9361Y
  255750. 116 (20)
  255751. McDonald, F. E.B
  255752. JACSC*Furan Synthesis
  255753. Molybdenum Carbene ComplexI
  255754. 21964N
  255755. 2/28/96VZMechanism of Molybdenum Pentacarbonyl-Catalyzed Cyclizations of Alkynols and Epoxyalkenes W
  255756. 1994X
  255757. 9363Y
  255758. 116 (20)
  255759. Nicolaou, K. C.B
  255760. JACSCHRadical Desulfurization
  255761. Oxocene Synthesis
  255762. Lewis Acid Induced CyclizationI
  255763. 21965N
  255764. 2/28/96V3Total Synthesis of Truncated Brevetoxin B [AFGHIJK]W
  255765. 1994X
  255766. 9371Y
  255767. 116 (20)
  255768. Paterson, IB
  255769. JACSCCMacrolactonization
  255770. Protecting Groups
  255771. Boron Enolates
  255772. Aldol ChemistryI
  255773. 21966N
  255774. 2/28/96V4Total Synthesis of Swinholide A and Hemiswinholide AW
  255775. 1994X
  255776. 9391Y
  255777. 116 (20)
  255778. Kagan, H. B.B
  255779. JACSI
  255780. 21967N
  255781. 2/28/96V)Nonlinear Effects in Asymmetric CatalysisW
  255782. 1994X
  255783. 9430Y
  255784. 116 (21)
  255785. Taber, D. F.B
  255786. JACSCDOrganozirconium Mediated Cyclization
  255787. Zirconium
  255788. Annulation
  255789. Diene
  255790. DiolI
  255791. 21968N
  255792. 2/28/96VpStereoselectivity in Intramolecular Diene Cycloaromatization :  A Combined Experimental and Theoretical ApproachW
  255793. 1994X
  255794. 9457Y
  255795. 116 (21)
  255796. Danheiser, R. L.B
  255797. JACSCuPhotochemical Annulation
  255798. Diazoketone
  255799. Alkyne
  255800. Phenol
  255801. Wolff rearrangement
  255802. [2+2] Cycloaddition
  255803. Electrocyclic Ring ClosureI
  255804. 21969N
  255805. 2/28/96V8Total Synthesis of the Phenalenone Diterpene SalvilenoneW
  255806. 1994X
  255807. 9471Y
  255808. 116 (21)
  255809. Houk, K. N.B
  255810. JACSC
  255811. Computational Chemistry
  255812. 21970N
  255813. 2/28/96
  255814. Theoretical Secondary Kinetic Isotope Effects and the Interpretation of Transition State Geometries. 2.  The Diels-Alder Reaction Transition State GeometryW
  255815. 1994X
  255816. 9675Y
  255817. Rodrigues, J. A. R.B
  255818. JACSC+Oxenium Ion Cyclization
  255819. Hypervalent Iodine
  255820. 21971N
  255821. 2/28/96VpSynthesis of Cularine and Sarcocapnine via Enium Ions and a New, Highly Diastereoselective Reductive MethylationW
  255822. 1994X
  255823. 9745Y
  255824. Negeshi, E-i
  255825. JACSC2Zirconium 
  255826. Organozirconium
  255827. Diene
  255828. Ketone
  255829. AnnulationI
  255830. 21972N
  255831. 2/28/96V@Nonconcerted paths for Reactions of Alkene Zirconocene ComplexesW
  255832. 1994X
  255833. 9751Y
  255834. Beak, PB
  255835. JACSC<Organolithium
  255836. Lithium
  255837. Carbanion
  255838. Chiral Ligand
  255839. OrganostannaneI
  255840. 21973N
  255841. 2/28/96V
  255842. Asymmetric Substitutions:  High and Opposite Enantioselective Alkyations of a Racemic Organolithium Intermediate in the Presence of (-)-SparteineW
  255843. 1994X
  255844. 9755Y
  255845. Mori, M.B
  255846. JACSC!Organonickel Mediated Annulation
  255847. Synthesis of 5-7 membered rings
  255848. 21974N
  255849. 2/28/96VnNovel Stereoselective Cylization via p-Allylnickel Complex Generated from 1,3-Diene and Hydride Nickel ComplexW
  255850. 1994X
  255851. 9771Y
  255852. Somfai, P.B
  255853. JACSC
  255854. Aziridine
  255855. CarbanionI
  255856. 21975N
  255857. 2/28/96V1Aza-[2,3] Wittig Rearrangement of VinylaziridenesW
  255858. 1994X
  255859. 9781Y
  255860. Weinreb, S. M.B
  255861. JACSCZOrganosilicon
  255862. Organostannane
  255863. Palladium Catalyzed Coulping
  255864. Lewis Acid Mediated Cyclization
  255865. KTMechanistically, reaction proceeds via a rare type of pericyclic concerted pathway. M
  255866. 21976N
  255867. 2/28/96VeTotal Synthesis of Papuamine via Stereospecific Intramolecular Imino Ene Reaction of an AllenylsilaneW
  255868. 1994X
  255869. 9789Y
  255870. Weinreb, S. M.B
  255871. JACSC,Organostannane
  255872. Palladium Catalyzed Coulping
  255873. K-See TL 1991, 32, 5681 and Chem. Lett. 1987, 5M
  255874. 21977N
  255875. 2/28/96VeTotal Synthesis of Papuamine via Stereospecific Intramolecular Imino Ene Reaction of an AllenylsilaneW
  255876. 1994X
  255877. 9791Y
  255878. Kobayashi, S.B
  255879. ^CbAsymmetric Aldol Condensation
  255880. Chiral Amine Ligand
  255881. Organotin Enolate
  255882. Silyl Ketene Acetal
  255883. Lewis AcidI
  255884. 21978N
  255885. 2/28/96V
  255886. Highly Enantioselective Synthesis of Enantionmeric 2,3-Dihdroxy Thioesters by Using Similar Types of Chiral Sources Derived from L-ProlineW
  255887. 1994X
  255888. 9805Y
  255889. White, J. DB
  255890. JACSC1Lewis Acid Mediated Polyene Cyclization
  255891. KetoesterI
  255892. 21979N
  255893. 2/28/96V
  255894. Construction of the Stemodane Nucleus by a Hydroxyl-Directed Intramolecular Ene Reaction.  Total Synthesis of (
  255895. )-2-DesoxystemodineW
  255896. 1994X
  255897. 9912Y
  255898. White, J. D.B
  255899. JACSC
  255900. Samarium Iodide Barbier Reaction
  255901. SmI2 Reduction
  255902. Huang-Minlon Reduction of Ketone
  255903. Annulation
  255904. Hydroxy Aldehyde
  255905. Thermal Ene Reaction
  255906. Lewis AcidI
  255907. 21980N
  255908. 2/28/96V
  255909. Construction of the Stemodane Nucleus by a Hydroxyl-Directed Intramolecular Ene Reaction.  Total Synthesis of (
  255910. )-2-DesoxystemodineW
  255911. 1994X
  255912. 9912Y
  255913. Bach, R. D.B
  255914. JACSC1Diels-Alder Cycloaddition Reaction
  255915. Isobenzofuran
  255916. 21981
  255917. 2/28/96V
  255918. Synthesis of (
  255919. )-FredericamycinW
  255920. 1994X
  255921. 9921Y
  255922. Bach, R. D.B
  255923. JACSCRMercury Mediated Pinacol Rearrangement
  255924. Dithioacetal
  255925. Bis Silyl enol Ether
  255926. 1,3-DioneI
  255927. 21982N
  255928. 2/28/96V
  255929. Synthesis of (
  255930. )-FredericamycinW
  255931. 1994X
  255932. 9921Y
  255933. Bach, R. D.B
  255934. JACSC:Benzylic Lithium Carbanion
  255935. Cuprate
  255936. Organocuprate
  255937. AcylationI
  255938. 21983N
  255939. 2/28/96V
  255940. Synthesis of (
  255941. )-FredericamycinW
  255942. 1994X
  255943. 9921Y
  255944. Bach, R. D.B
  255945. JACSCHMichael Condensation
  255946. Lithium Carbanion
  255947. Annulation
  255948. Dieckmann CondensationI
  255949. 21984N
  255950. 2/28/96V
  255951. Synthesis of (
  255952. )-FredericamycinW
  255953. 1994X
  255954. 9921Y
  255955. Tietze, L. F. B
  255956. JACSCJChiral Allylsilane 
  255957. Ketone
  255958. Homoallylic Alcohol
  255959. Sodium Reduction
  255960. Lewis AcidI
  255961. 21985N
  255962. 2/28/96VvEnantioselective Synthesis of Tertiary Homoallylic Alcohols via Diastereoselective Addition of Allylsilanes to KetonesW
  255963. 1995X
  255964. 5851Y
  255965. GABRIEL WEATHERHEADw
  255966. Ketone to Homoallylic Alcohol
  255967. Grubbs, R. H.B
  255968. fCZRuthenium Carbene Transition Metal Complex
  255969. Alkene Metathesis
  255970. Olefin Metathesis
  255971. Annulation
  255972. Only the (S,S,S) diastereomer cyclizes in the metathesis reaction.  Under the same conditions the (R,S,R)  diastereomer is recovered unchanged.M
  255973. 21986N
  255974. 2/28/96V]Synthesis of Conformationally Restricted Amino Acids and Peptides Employing Olefin MetathesisW
  255975. 1995X
  255976. 5855Y
  255977. GABRIEL WEATHERHEADw
  255978. Diene to Alkene
  255979. Creary, X.B
  255980. JACSCKAcyl Anion Equivalent
  255981. Directed Metalation
  255982. Acyl thioamide
  255983. Lithium Carbanion
  255984. Enhanced kinetic acidity via coordination of the LDA to the thioamide S atom accounts for the formation of the thiolactam product.M
  255985. 21987N
  255986. 2/28/96
  255987. AOFormation and Cyclization of Acyl Thioamides.  A Novel b-Lactam Forming Process
  255988. 1995X
  255989. 5859Y
  255990. GABRIEL WEATHERHEAD
  255991. Takahashi, T.B
  255992. hCZZirconium Complex
  255993. Organozirconium
  255994. Carbometalation
  255995. Alkyne
  255996. Diene Synthesis
  255997. Vinylzirconation
  255998. 6K5Electrophiles used were either  iodine or acid quenchM
  255999. 21988N
  256000. 2/28/96V&A Vinylzirconation Reaction of AlkynesW
  256001. 1995X
  256002. 5871Y
  256003. GABRIEL WEATHERHEADw
  256004. Alkyne to Diene
  256005. Waymouth, R. M.B
  256006. JACSClZielger-Natta Catalyst
  256007. Ziconium Complex
  256008. Organozirconium 
  256009. Aluminum Reagent 
  256010. Organoaluminum Annulation
  256011. Diene 
  256012. 7KSProceeds through an organoaluminum species which is oxidized in the presence of airM
  256013. 21989N
  256014. 2/28/96
  256015. ACCarbometalation of a,w-Dienes and Olefins Catalyzed by Zirconocenes
  256016. 1995X
  256017. 5873Y
  256018. GABRIEL WEATHERHEADw
  256019. Diene to Alcohol
  256020. Jacobsen, E. N.B
  256021. JACSC
  256022. Aziridine
  256023. Nitrene
  256024. PhI=NTs
  256025. 21990N
  256026. 2/28/96V
  256027. Mechanism of the (Diimine)copper-Catalyzed Asymmetric Aziridination of Alkenes.  Nitrene Transfer via Ligand-Accelerated CatalysisW
  256028. 1995X
  256029. 5889Y
  256030. GABRIEL WEATHERHEADw
  256031. Alkene to Aziridine
  256032. Jacobsen, E. N.B
  256033. JACSCNEpoxide Ring Opening
  256034. Azide
  256035. Chromium  Salen Complex
  256036. Asymmetric 
  256037. Chiral
  256038. Alcohol
  256039. 21991N
  256040. 2/28/96VVHighly Enantioselective Ring Opening of Epoxides Catalyzed by (salen)Cr(III) ComplexesW
  256041. 1995X
  256042. 5897Y
  256043. GABRIEL WEATHERHEADw
  256044. Epoxide to Azido Alcohol
  256045. David P. RotellaB
  256046. Tet. Lett.CAReduction
  256047. a-haloketone
  256048. oxirane
  256049. bromoethylene ketone
  256050. amino alcoholI
  256051. KrNaBH4 in EtOH gave 97:3 ratio of 7e to 7t
  256052. Most other reagents(DiBAL-H, LAHOtBu3,...) gave about 1:1 or at most 8:1M
  256053. 22092N
  256054. 2/28/96V5Stereoselective Synthesis of Erythro a-Amino EpoxidesW
  256055. 1995X
  256056. 5453Y
  256057. GABRIEL WEATHERHEADwLbromoalcohol -> epoxide
  256058. bromoketone -> bromoalcohol
  256059. aminoacid -> bromoketone
  256060. J.M. Williams, et al.B
  256061. Tet. Lett.CPWeinreb
  256062. s amide
  256063. Grignard
  256064. N,O-dimethylhydroxylamine
  256065. organomagnesium
  256066. lithium amideI
  256067. K[In general, the yields are >90%.
  256068. R = Ph, Bn, and other hindered pi containing functionality
  256069. 22093N
  256070. 2/28/96VvA New Method for the Preparation of N-Methoxy-N-Methylamides. Application in Direct Conversion of an ester to a KetoneW
  256071. 1995X
  256072. 5461Y
  256073. GABRIEL WEATHERHEADw.ester -> amide
  256074. ester -> ketone
  256075. amide -> ketoney
  256076. Merck Process
  256077. Philip Magnus
  256078. Michael B. RoeB
  256079. Tet. Lett.C7hydrazone
  256080. shapiro
  256081. tosyl hydrazone
  256082. diene
  256083. a,b unsaturatedI
  256084. K1yields generally >65%
  256085. E= DMF, Me3SiCl, adamantoneM
  256086. 22094N
  256087. 2/28/96VZConversion of Saturated Ketones into 2-Lithiodienes via N,N-Bis-Tosylhydrazone DerivativesW
  256088. 1995X
  256089. 5479Y
  256090. GABRIEL WEATHERHEADw#ketone -> diene
  256091. ketone -> hydrazoney
  256092. U. Texas at Austin
  256093. Alan R. Katritzsky
  256094. et al.B
  256095. Tet. Lett.C
  256096. 1,4 addition
  256097. KME = n-decane, Bn, p-ClBn, PhCO, PhCHOH, PhNHCS, Ph2COH
  256098. Bt = benzotriazol-1-ylM
  256099. 22095N
  256100. 2/28/96VXA Versatile One-pot Procedure for the Insertion of a 3-Substituent into 2-CycloalkenonesW
  256101. 1995X
  256102. 5491Y
  256103. GABRIEL WEATHERHEADy
  256104. U of Florida Gainesville
  256105. Taber, D. F.B
  256106. C1C-H Insertion
  256107. Rhodium Carbene Complex
  256108. Diazoester
  256109. ,The diazoester was prepared from the corresponding ester through a two step procedure involving benzoylation (NaH, PhCOOMe) then diazo transfer with p-nitrobenzenesulfonylazide in the presence of DBU.  The rhodium mediated C-H insertion of the above diazoester was found to be highly stereoselective.
  256110. 22096N
  256111. 2/28/96VqHighly Diastereoselective Cyclopentane Construction:  Enantioselective Synthesis of the Dendrobatid Alkaloid 251FW
  256112. 1995X
  256113. 5757Y
  256114. GABRIEL WEATHERHEAD
  256115. Taber, D. F.B
  256116. JACSCELithium Ester E nolate
  256117. Intramolecular Alkylation 
  256118. Diastereoselective I
  256119. 22097N
  256120. 2/28/96VqHighly Diastereoselective Cyclopentane Construction:  Enantioselective Synthesis of the Dendrobatid Alkaloid 251FW
  256121. 1995X
  256122. 5757Y
  256123. GABRIEL WEATHERHEAD
  256124. Doyle, M. P.B
  256125. JACSC@Chiral Rhodium Carbene Complex
  256126. Diazoester
  256127. Cyclopropane SynthesisI
  256128. 22098N
  256129. 2/28/96
  256130. Enantioselective Intramolecular Cyclopropanations of Allylic and Homoallylic Diazoacetates and Diazoacetamides Using Chiral Dirhodium (II) Carboxamide CatalysisW
  256131. 1995X
  256132. 5763Y
  256133. GABRIEL WEATHERHEAD
  256134. Tietze, L. F. B
  256135. JACSCJChiral Allylsilane 
  256136. Ketone
  256137. Homoallylic Alcohol
  256138. Sodium Reduction
  256139. Lewis AcidI
  256140. 22099N
  256141. 2/28/96VvEnantioselective Synthesis of Tertiary Homoallylic Alcohols via Diastereoselective Addition of Allylsilanes to KetonesW
  256142. 1995X
  256143. 5851Y
  256144. GABRIEL WEATHERHEADw
  256145. Ketone to Homoallylic Alcohol
  256146. Grubbs, R. H.B
  256147. JACSCZRuthenium Carbene Transition Metal Complex
  256148. Alkene Metathesis
  256149. Olefin Metathesis
  256150. Annulation
  256151. Only the (S,S,S) diastereomer cyclizes in the metathesis reaction.  Under the same conditions the (R,S,R)  diastereomer is recovered unchanged.M
  256152. 22100N
  256153. 2/28/96V]Synthesis of Conformationally Restricted Amino Acids and Peptides Employing Olefin MetathesisW
  256154. 1995X
  256155. 5855Y
  256156. GABRIEL WEATHERHEADw
  256157. Diene to Alkene
  256158. Creary, X.B
  256159. JACSCKAcyl Anion Equivalent
  256160. Directed Metalation
  256161. Acyl thioamide
  256162. Lithium Carbanion
  256163. Enhanced kinetic acidity via coordination of the LDA to the thioamide S atom accounts for the formation of the thiolactam product.M
  256164. 22101N
  256165. 2/28/96
  256166. AOFormation and Cyclization of Acyl Thioamides.  A Novel b-Lactam Forming Process
  256167. 1995X
  256168. 5859Y
  256169. GABRIEL WEATHERHEAD
  256170. Takahashi, T.B
  256171. JACSCZZirconium Complex
  256172. Organozirconium
  256173. Carbometalation
  256174. Alkyne
  256175. Diene Synthesis
  256176. Vinylzirconation
  256177. 6K5Electrophiles used were either  iodine or acid quenchM
  256178. 22102N
  256179. 2/28/96V&A Vinylzirconation Reaction of AlkynesW
  256180. 1995X
  256181. 5871Y
  256182. GABRIEL WEATHERHEADw
  256183. Alkyne to Diene
  256184. Waymouth, R. M.B
  256185. JACSClZielger-Natta Catalyst
  256186. Ziconium Complex
  256187. Organozirconium 
  256188. Aluminum Reagent 
  256189. Organoaluminum Annulation
  256190. Diene 
  256191. KSProceeds through an organoaluminum species which is oxidized in the presence of airM
  256192. 22103N
  256193. 2/28/96
  256194. ACCarbometalation of a,w-Dienes and Olefins Catalyzed by Zirconocenes
  256195. 1995X
  256196. 5873Y
  256197. GABRIEL WEATHERHEADw
  256198. Diene to Alcohol
  256199. Jacobsen, E. N.B
  256200. JACSC
  256201. Aziridine
  256202. Nitrene
  256203. PhI=NTs
  256204. 22104N
  256205. 2/28/96V
  256206. Mechanism of the (Diimine)copper-Catalyzed Asymmetric Aziridination of Alkenes.  Nitrene Transfer via Ligand-Accelerated CatalysisW
  256207. 1995X
  256208. 5889Y
  256209. GABRIEL WEATHERHEADw
  256210. Alkene to Aziridine
  256211. Jacobsen, E. N.B
  256212. JACSCNEpoxide Ring Opening
  256213. Azide
  256214. Chromium  Salen Complex
  256215. Asymmetric 
  256216. Chiral
  256217. Alcohol
  256218. 22105N
  256219. 2/28/96VVHighly Enantioselective Ring Opening of Epoxides Catalyzed by (salen)Cr(III) ComplexesW
  256220. 1995X
  256221. 5897Y
  256222. GABRIEL WEATHERHEADw
  256223. Epoxide to Azido Alcohol
  256224. A    Stork, G.B
  256225. JACSC4Diels-Alder Reaction
  256226. Organomagnesium
  256227. Organoaluminum
  256228. 22106
  256229. 2/28/96VBTemporary Magnesium and Aluminum Connections in 4+2 CycloadditionsW
  256230. 1995X
  256231. 6595Y
  256232. GABRIEL WEATHERHEAD
  256233. Curran, D. P.B
  256234. JACSC:Radical Reaction
  256235. Silicon Hydride
  256236. Organotin
  256237. Photochemistry
  256238. 22107N
  256239. 2/28/96V
  256240. Controlling Radical Chain Reactions by Unimolecular Chain Transfer.  Intramolecular Hydrogen Transfer Reactions of Silicon HydridesW
  256241. 1995X
  256242. 6603Y
  256243. GABRIEL WEATHERHEAD
  256244. McDonald, F. E.B
  256245. JACSCmC-Aryl Glycoside
  256246. Rhodium Mediated Cyclotrimerization
  256247. Transition Metal
  256248. Diyne
  256249. Annulation
  256250. Wilkinson
  256251. s Catalyst
  256252. 22108N
  256253. 2/28/96VTRhodium-Catalyzed Alkyne Cyclotrimerization Strategies for C-Arylglycoside SynthesisW
  256254. 1995X
  256255. 6605Y
  256256. GABRIEL WEATHERHEADw
  256257. Alkyne to Arene
  256258. Renaud, P.B
  256259. JACSCSRadical
  256260. Chelation Control
  256261. Lewis Acid
  256262. Hydrogen Transfer
  256263. Felkin-Anh Model
  256264. Cram Model
  256265. 22109N
  256266. 2/28/96VfStereoselectivity in Reactions of 1,2-Dioxy-Substituted Radicals:  Electronic versus Chelation ControlW
  256267. 1995X
  256268. 6607Y
  256269. GABRIEL WEATHERHEAD
  256270. Evans, D. A.B
  256271. JACSC
  256272. Organostannane
  256273. Lithium Enolate
  256274. Boron Enolate
  256275. Grignard Reagent
  256276. Silyl Enol Ether
  256277. Felkin-Anh 
  256278. Transition State
  256279. Allyl Stannane
  256280. Aldol Reaction
  256281. Ratio
  256282. s are Felkin/anti-FelkinM
  256283. 22110N
  256284. 2/28/96
  256285. Diastereoselective Aldol and Allylsilane Addition Reactions.  The Merged Stereochemical Impact of a and b Aldehyde Substituents
  256286. 1995X
  256287. 6619Y
  256288. GABRIEL WEATHERHEAD
  256289. Overman, L. E.B
  256290. JACSCVIntramolecular Prins  Rxn
  256291. Annulation
  256292. Lewis Acid
  256293. Oxonium ion Cyclization
  256294. (+)-Laurencin
  256295. 22111N
  256296. 2/28/96V
  256297. Total Synthesis of (+)-Laurencin.  Use of Acetal-Vinyl Sulfide Cyclizations for Forming Highly Functionalized Eight-Membered Cyclic EthersW
  256298. 1995X
  256299. 5958Y
  256300. GABRIEL WEATHERHEADw
  256301. Acetal to Cyclic Ether
  256302. Falck, J. R.B
  256303. CECopper Cyanide
  256304. Organocopper
  256305. Stannane
  256306. Organostannane
  256307. Transmetalation
  256308. 22112N
  256309. 2/28/96
  256310. AqTin-Copper Transmetalation:  Cross-Coupling of a-Heteroatom-Substituted Alkyltributylstannanes with Organohalides
  256311. 1995X
  256312. 5973Y
  256313. GABRIEL WEATHERHEADw
  256314. Alkyl Tin to Thioester
  256315. Lipshutz, B.H.B
  256316. JACSCELithium Carbanion
  256317. Organozinc
  256318. Higher Order Cuprate
  256319. Conjugate Addition
  256320. KINMR study indicates the formation of a higher order cuprate after step 3.M
  256321. 22113N
  256322. 2/28/96VfMichael Additions of Functionalized Organozinc Reagents Mediated by Catalytic Quantities of Copper (I)W
  256323. 1995X
  256324. 6126Y
  256325. GABRIEL WEATHERHEAD
  256326. Shibasaki, M.B
  256327. JACSCdNitro Aldol reactionMichael Addition
  256328. Conjugate Addition
  256329. Chiral Lanthanide Catalyst
  256330. BINOL
  256331. Lewis Acid
  256332. Synthesis of (R)-LSB complex:  (R)-BINOL in THF was added to La(i-PrO)3 at 0
  256333. C.  After stirring for 5 min. at room temperature,  Na(Ot-Bu) was added in THF at 0
  256334. C.  X-ray structure of the complex (LSB) was also obtained.
  256335. 22114N
  256336. 2/28/96V?The First Heterobimetallic Multifunctional Asymmetric CatalysisW
  256337. 1995X
  256338. 6194Y
  256339. GABRIEL WEATHERHEAD
  256340. Keck, G. E.B
  256341. JACSC[Organostannane
  256342. Stannane
  256343. Aldehyde
  256344. Lewis Acid
  256345. Allyl Stannane
  256346. Annulation
  256347. Chelation ControlI
  256348. E isomer provides under thermal conditions 80% of 18, however, under Lewis Acid conditions 17 is the major product formed.  Product stereochemistry is sensitive to both olefin geometry and Lewis acid.  In the synclinal transition state there is the possibility for secondary orbital overlap (which the antiperiplanar TS cannot participate in) between the aldehyde carbonyl and the stannyl methylene.  The secondary orbital overlap will be most important for Lewis acids which result in the largB
  256349. est decrease in energy for the carbonyl p* LUMO.  In the case where phenyl has been replaced by OBn there is the opportunity for a chelation control mechanism. 
  256350. 22115N
  256351. 2/28/96V
  256352. Intramolecular Allylstannane-Aldehyde Cyclizations:  Stereochemical Results with Flexible Tethers for Reactions Forming VinylcyclohexanolsW
  256353. 1995X
  256354. 6210Y
  256355. GABRIEL WEATHERHEADw9Aldehyde to Homoallylic Alcohol 
  256356. Allylstannane to Alcohol
  256357. White, J. D.B
  256358. JACSC8Tin tetrachloride
  256359. Epoxide Ring Opening
  256360. Cyclopropanation
  256361. 22116N
  256362. 2/28/96
  256363. Cyclopropane-Containing Eicosanoids of Marine Orgin.  Biomimetic Synthesis of Constanolactones A and B from the Alga Constantinea simplex
  256364. 1995X
  256365. 6224Y
  256366. GABRIEL WEATHERHEAD
  256367. White, J. D.B
  256368. JACSC8Nozaki Kishi Reaction
  256369. Nickel Chloride
  256370. Chromium Chloride
  256371. K*Major diastereomer has (9S) configuration.M
  256372. 22117N
  256373. 2/28/96
  256374. Cyclopropane-Containing Eicosanoids of Marine Orgin.  Biomimetic Synthesis of Constanolactones A and B from the Alga Constantinea simplex
  256375. 1995X
  256376. 6224Y
  256377. GABRIEL WEATHERHEADw4Aldehyde to Alcohol 
  256378. Vinyl Iodide to Allylic Alcohol
  256379. Noyori, R.B
  256380. C6Organozinc
  256381. Chiral Zinc Reagent
  256382. Amino Alcohol Catalyst
  256383. 22118N
  256384. 2/28/96ViAn Ab Initio Molecular Orbital Study on the Amino Alcohol-Promoted Reaction of Dialkylzincs and AldehydesW
  256385. 1995X
  256386. 6327Y
  256387. GABRIEL WEATHERHEADw
  256388. Aldehyde to Alcohol
  256389. Negishi, E. I.B
  256390. A?Palladium Cyclization
  256391. Allene
  256392. p-Allyl Pd Intermediate
  256393. Annulation
  256394. uPalladium mediated cyclization occurs to provide products which have 5 through 12 membered rings including a product containing a 20 membered ring.  The cyclization proceeds to react at the central carbon of the allene in all cases studied.  The Pd p-allyl intermediates can be trapped with various nucleophiles such as malonate esters, organostannanes, phenols and amines.
  256395. 22119N
  256396. 2/28/96
  256397. Palladium-Catalyzed Cyclization of w- Halloallenes.  A New General Route to Common, Medium and Large Ring Compounds via Cyclic Carbopalladation
  256398. 1995X
  256399. 6345Y
  256400. GABRIEL WEATHERHEADw
  256401. Allene to Diene
  256402. Kobayashi, S.B
  256403. JACSC*Allene 
  256404. Acetylene
  256405. Organosilicon
  256406. Silicon
  256407. 22120N
  256408. 2/28/96V
  256409. Selective Formation of Propargylsilanes and Allenylsilanes and Their Reactions with Aldehydes for the Preparation of Homopropargylic and Allenic AlcoholsW
  256410. 1995X
  256411. 6392Y
  256412. GABRIEL WEATHERHEAD
  256413. Shibasaki, M.B
  256414. JOCChAldol Condensation
  256415. Silyl Enol Ether
  256416. Chiral Palladium Catalyst
  256417. Silver Triflate
  256418.  Transition Metal Enolate
  256419. 22121N
  256420. 2/28/96VICatalytic Asymmetric Aldol Reaction via Chiral Pd (II) Enolate in Wet DMFW
  256421. 1995X
  256422. 2648Y
  256423. GABRIEL WEATHERHEAD
  256424. Comins, D. L.B
  256425. CYEnol Triflate
  256426. Lithium Amide Enolate
  256427. Organocopper
  256428. Palladium 
  256429. Reduction TBTH
  256430. Carbonylation
  256431. 22122N
  256432. 2/28/96
  256433. AdSynthesis and Reactions of a-(Trifluoromethanesulfonyloxy) Enecarbamates Prepared From N-Acyllactams
  256434. 1995X
  256435. 2656Y
  256436. GABRIEL WEATHERHEADw
  256437. Lactam to Enol Triflate
  256438. Sato, F.B
  256439. JOCCcOrganozinc
  256440. Chelation Control (syn)
  256441. Epoxide
  256442. Diastereoselective
  256443. Organometallic
  256444. Felkin-Anh (anti)I
  256445. 22123N
  256446. 2/28/96
  256447. AJChelation-Controlled Addition of Dialkylzincs to trans-a,b-Epoxy Aldehydes
  256448. 1995X
  256449. 2660Y
  256450. GABRIEL WEATHERHEAD
  256451. Marshall, J. A.B
  256452. JOCCTOrganostannane
  256453. Allylstannane
  256454. Higher Order Cuprate
  256455. Conjugate Addition
  256456. Lewis Acid
  256457. 22124N
  256458. 2/28/96
  256459. Interconversion of Nonracemic a-OTBS Crotyl and g-OTBS Methallyl Tri-n-butylstannanes.  Additions of the (E)-Methallyl Isomer to Representative Aldehydes
  256460. 1995X
  256461. 2662Y
  256462. GABRIEL WEATHERHEADw
  256463. Aldehyde -  Homoallylic Alcohol
  256464. Malacria, M.B
  256465. JOCCXPalladium Cyclization
  256466. Organocobalt  
  256467. Co(I) Cyclotrimerization
  256468. Intramolecular Diels-AlderI
  256469. 22125N
  256470. 2/28/96V
  256471. A New Cyclization Reaction Cascade:  Ene Type, [2+2+2], [4+2].  Stereoselective Formation of Six Carbon-Carbon Bonds and Four Rings in a One-Pot Sequence W
  256472. 1995X
  256473. 2664Y
  256474. GABRIEL WEATHERHEAD
  256475. Zhao, K.B
  256476. JOCCMPotassium Enolate
  256477.  Alkylation
  256478. Diastereoselective O-Alkylation
  256479. Enol Ether
  256480. 22126N
  256481. 2/28/96V11,3-Diastereoselective O-Displacement of EnolatesW
  256482. 1995X
  256483. 2668Y
  256484. GABRIEL WEATHERHEAD
  256485. A    Padwa, A.B
  256486. CNRhodium Carbene Complex
  256487. Transition Metal
  256488. [3+2] Cycloaddition
  256489. Diazo Amide EsterI
  256490. 22127N
  256491. 2/28/96V[An Approach to Lysergic Acid Utilizing an Intramolecular Isomunchnone Cycloaddition PathwayW
  256492. 1995X
  256493. 2704Y
  256494. GABRIEL WEATHERHEAD
  256495. Knochel, P.B
  256496. JOCCFAllylchromium (III) Reagent
  256497. Organochromium
  256498. Chromium
  256499. Allylic PhosphatesI
  256500. 2.5 equivalents of CrCl2M
  256501. 22128N
  256502. 2/28/96V`Chromium(II)-Mediated Stereodivergent Additions of Allylic Phosphates and Halides to Aldehydes. W
  256503. 1995X
  256504. 2762Y
  256505. GABRIEL WEATHERHEADw
  256506. Aldehyde -  Homoallylic Alcohol
  256507. Knochel, P.B
  256508. SynlettC;Zinc
  256509. Organozinc
  256510. Palladium Catalyst 
  256511. Cuprate
  256512. Nickel CatalystK
  256513. ReviewM
  256514. 22129N
  256515. 2/28/96VBStereoselective Reactions Mediated by Functionalized DiorganozincsW
  256516. 1995X
  256517. GABRIEL WEATHERHEAD
  256518. Jones, G. B.B    SynthesisC/Chiral Auxiliary
  256519. Asymmetric Induction
  256520. Catalyst
  256521. ReviewM
  256522. 22130N
  256523. 2/28/96
  256524. A*p Stacking Effects in Asymmetric Synthesis
  256525. 1995X
  256526. GABRIEL WEATHERHEAD
  256527. Sharpless, K. B.B
  256528. Angew. Chem. Int. Ed. Engl. C@Titanium Asymmetric Epoxidation
  256529. Osmium Tetroxide Dihyroxylation
  256530. ReviewM
  256531. 22131N
  256532. 2/28/96V
  256533. Ligand-Accelerated CatalysisW
  256534. 1995X
  256535. 1059Y
  256536. GABRIEL WEATHERHEAD
  256537. Yamamoto, Y.B
  256538. J.C.S. Chem. Commun.
  256539. Organostannane
  256540. Homoallylic Alcohol
  256541. Organopalladium  Catalyst
  256542. Allylstannane
  256543. Aldehyde
  256544. Ketone
  256545. Bis(p-Allyl) Palladium 
  256546. Organoplatinum
  256547. 22132N
  256548. 2/28/96VKPalladium- and Platinum-Catalyzed Addition of Aldehydes with AllylstannanesW
  256549. 1995X
  256550. 1273a
  256551. GABRIEL WEATHERHEADw Aldehyde to Homoallylic Alcohol 
  256552. Larock, R. C.B
  256553. JOCC4Palladium Catalyst
  256554. Cyclization
  256555. Alkyne
  256556. Heck Reaction
  256557. 22133N
  256558. 2/28/96VYSynthesis of Aromatic Heterocycles via Palladium-Catalyzed Annulation of Internal AlkynesW
  256559. 1995X
  256560. 3270Y
  256561. GABRIEL WEATHERHEAD
  256562. A    Luh, T-Y.B
  256563. CyDithioacetal
  256564. Dithiane
  256565. Grignard 
  256566. Nickel Coupling
  256567. Organonickel
  256568. Diene Synthesis
  256569. Tamao Oxidation
  256570. Silicon tethered Diels-AlderI
  256571. 22134N
  256572. 2/28/96V
  256573. Novel Synthesis of Dienylsiloxanes.  Stereoselective Synthesis of 3-Cyclohexene-1,2-diols by Intramolecular Diels-Alder Reactions of Siloxane-Tethered Bis-DienesW
  256574. 1995X
  256575. 3272Y
  256576. GABRIEL WEATHERHEAD
  256577. Moore, H. W.B
  256578. JOCC|Electrocyclization
  256579. Allene
  256580. Organolithium
  256581. Lithium Carbanion
  256582. Oxy-anion Electrocyclic Ring Opening
  256583. Enolate
  256584. Napthalene Synthesis
  256585. 22135N
  256586. 2/28/96V
  256587. Stereocontrolled Synthesis of 3-Acyl-4-alkoxy-5-aryl-1,2,4(E)-pentatrienes and Their Subsequent Electrocyclization to NaphthalenesW
  256588. 1995X
  256589. 3274Y
  256590. GABRIEL WEATHERHEAD
  256591. Srebnik, M.B
  256592. JOCC]Hydrozirconation
  256593. Suzuki Coupling
  256594. Palladium Catalyst
  256595. Boronic Ester
  256596. Acetylene
  256597. Alkene Synthesis
  256598. 22136N
  256599. 2/28/96VzStereospecific Synthesis of Temarotene, Its Structural Isomers, and Mixed Triaryl Alkenes from gem-Borazirconocene AlkenesW
  256600. 1995X
  256601. 3276Y
  256602. GABRIEL WEATHERHEADw
  256603. Acetylene to Alkene
  256604. Srebnik, M.B
  256605. JOCC0Organozirconium
  256606. Zirconium
  256607. Zinc Bromide
  256608. OxidationI
  256609. 22137N
  256610. 2/28/96V
  256611. 1,2-Addition of Alkyl- and Alkenylzirconocene Chlorides to Aldehydes Accelerated by Catalytic Amounts of ZnBr2 as a Method of Synthesizing Secondary Allylic Alcohols, and in-situ Oppenauer-Type Oxidation of the Alcohols to KetonesW
  256612. 1995X
  256613. 3278Y
  256614. GABRIEL WEATHERHEADw&Aldehyde to Ketone
  256615. Aldehyde to Alcohol
  256616. Paterson, I. B
  256617. Ireland Claisen Rearrangement
  256618. 83% yield, dr = 96/4 M
  256619. 22138N
  256620. 2/28/96V*Total Synthesis of (-)-Ebelacatone A and BW
  256621. 1995X
  256622. 3288Y
  256623. GABRIEL WEATHERHEAD
  256624. Paterson, I. B
  256625. JOCCqSyn Aldol
  256626. Anti Aldol
  256627. Boron Enolate
  256628. Felkin Adduct
  256629. Lewis Acid
  256630. Diastereoselective Hydrogenation
  256631. Wilkinson
  256632. s CatalystI
  256633. 22139N
  256634. 2/28/96V*Total Synthesis of (-)-Ebelacatone A and BW
  256635. 1995X
  256636. 3288Y
  256637. GABRIEL WEATHERHEAD
  256638. Knochel, P.B
  256639. CKOrganozinc
  256640. Hydroboration
  256641. Cuprate
  256642. Acylation
  256643. Michael Addition
  256644. AlkylationI
  256645. 22140N
  256646. 2/28/96VHPreparation and Reactions of Diorganozincs from Dienic Silyl Enol EthersW
  256647. 1995X
  256648. 3311Y
  256649. GABRIEL WEATHERHEAD
  256650. Lipshutz, B. H.B
  256651. JOCCpElectrophile
  256652. Organoselenium
  256653. 5-Endo-trig Cyclization
  256654. Tetrahydrofuran 
  256655. Selenium Ion Ring Closure
  256656. Radical ReductionI
  256657. 22141N
  256658. 2/28/96
  256659. (2,4,6-Triisopropylphenyl)selenium Bromide (TIPPSe-Br).  An in Situ-Generated Reagent for Effecting Highly Selective Ring Closures of Homoallylic Alcohols to Substituted Tetrahydrofurans
  256660. 1995X
  256661. 3572Y
  256662. GABRIEL WEATHERHEAD
  256663. Denmark, S. E.B
  256664. JOCCXTandem [4+2] [3+2] Nitroalkene Cycloaddition
  256665. Orgnoaluminum Catalyst 
  256666. Lewis Acid
  256667. AluminumI
  256668. Other references:  Denmark JOC 1995, 60, 3205
  256669.                                                                JOC 1995, 60, 3221
  256670. 22142N
  256671. 2/28/96VpA General Strategy for the Synthesis of Cis-Substituted Pyrrolizidine Bases.  The Synthesis of (-)-RosmarinecineW
  256672. 1995X
  256673. 3574Y
  256674. GABRIEL WEATHERHEAD
  256675. Sato, F.B
  256676. JOCCd Radical Chemistry
  256677. Tributyltin Hydride
  256678. Organoaluminum
  256679. Chiral Lewis Acid
  256680. Asymmetric Addition
  256681. AluminumI
  256682. K!Various Lewis acids were studied M
  256683. 22143N
  256684. 2/28/96
  256685. AYLewis Acid-Enhanced Reactivity of a,b-Unsaturated Ester and Amide Toward Radical Addition
  256686. 1995X
  256687. 3576Y
  256688. GABRIEL WEATHERHEADw
  256689. Unsaturated Lactone to Lactone
  256690. Ziegler, F. E.B
  256691. JOCCVConjugate Addition
  256692. Organozinc
  256693. Unsaturated Ketone
  256694. Nickel acac
  256695. Luche Method
  256696. OrganonickelI
  256697. AiOther cuprate reagents gave either SM or 1,2 addition product.
  256698. Ref.:  Luche J. Org. Chem. 1985, 50, 5761.
  256699. 22144N
  256700. 2/28/96VIThe Total Synthesis of (
  256701. )-Scopadulcic Acids A and B and (
  256702. )-ScopadulciolW
  256703. 1995X
  256704. 3626Y
  256705. GABRIEL WEATHERHEAD
  256706. Roush, W. R.B
  256707. JOCCbAllylboronate
  256708. Organoboron
  256709. Homoallylic Alcohol
  256710. Tartarate Chiral Auxiliary
  256711. Allylmetal Reagent
  256712. Boron
  256713. 22145N
  256714. 2/28/96V
  256715. -Bis(2,2,2-trifluoroethyl)-N,N
  256716. -ethylenetartramide:  An Improved Chiral Auxiliary for the Asymmetric Allylboration ReactionW
  256717. 1995X
  256718. 3806Y
  256719. GABRIEL WEATHERHEADw
  256720. Aldehyde to Homoallylic Alcohol
  256721. Frost, C. G.
  256722. Williams, J. M. J.B
  256723. Contemporary Organic SynthesisC
  256724. Diels-Alder
  256725. Palladium 
  256726. Epoxidation Dihydroxylation
  256727. Hydrogenation
  256728. Friedel-Crafts
  256729. Hydroboration
  256730. Oxidation
  256731. Nucleophilic Additions
  256732. Carbonylation
  256733. Metal Carbenoids
  256734. ReviewM
  256735. 22146N
  256736. 2/28/96V@Catalytic Applications of Transition Metals in Organic SynthesisW
  256737. 1995X
  256738. GABRIEL WEATHERHEAD
  256739. Kozikowski, A. P.B
  256740. CePalladium Heck Reaction
  256741. Benzofuran Synthesis
  256742. Mitsunobu Coupling
  256743. Directed Metalation
  256744. Lithium CarbanionI
  256745. 22147N
  256746. 2/28/96V
  256747. Effect of Alteration of the Heterocyclic Nucleus of ILV on Its Isoform Selectivity for PKC.  Palladium-Catalyzed Route to Benzofuran Analogues of ILVW
  256748. 1995X
  256749. 6666Y
  256750. GABRIEL WEATHERHEAD
  256751. Buchwald, S. L.B
  256752. JACSC^Organotitanium
  256753. Silane Reduction
  256754. Annulation
  256755. Titanacycle
  256756. Transition Metal  Reductive CyclizationI
  256757. K-6/1 cyclization products to reduction productM
  256758. 22148N
  256759. 2/28/96V4Reductive Cyclization of Enones by Titanium CatalystW
  256760. 1995X
  256761. 6785Y
  256762. GABRIEL WEATHERHEADw
  256763. Ketone Alkene -> Alcohol
  256764. Crowe, W. E.B
  256765. JACSCrOrganotitanium
  256766. Silane Reduction
  256767. Annulation
  256768. Titanacycle
  256769. Transition Metal  Reductive Cyclization
  256770. MetallocyclopentaneI
  256771. 22149N
  256772. 2/28/96
  256773. AQTitanium-Catalyzed Reductive Cyclization of d,e-Unsaturated Ketones and Aldehydes
  256774. 6787Y
  256775. GABRIEL WEATHERHEADw3Ketone Alkene -> Alcohol
  256776. Aldehyde Alkyne -> Alcohol
  256777. A    Ojima, I.B
  256778. JACSCnIntramolecular 
  256779. Cyclization
  256780. Silylformylation
  256781. Organorhodium Catalyst
  256782. Rhodium Catalyst
  256783. Annulation
  256784. Silicon TetherI
  256785. 22150N
  256786. 2/28/96VCExtremely Regioselective Intramolecular Silylformylation of AlkynesW
  256787. 1995X
  256788. 6797Y
  256789. GABRIEL WEATHERHEADw
  256790. Alkyne ->Alkene Aldehyde
  256791. Lautens, M.B
  256792. JACSCqOrganocobalt
  256793. Cobalt acac Catalyzed Cycloaddition
  256794. Annulation
  256795. AsymmetricCyclizations
  256796. Chiral Ligand
  256797. Phosphine LigandI
  256798. 22151N
  256799. 2/28/96
  256800. AnCobalt-Catalyzed [2p+2p+2p] (Homo Diels-Alder) and [2p+2p+4p] Cycloaddition of Bicyclo[2.2.1.]hepta-2.5-dienes
  256801. 1995X
  256802. 6863Y
  256803. GABRIEL WEATHERHEAD
  256804. Danishefsky, S. J.B
  256805. JACSC)Organoboron
  256806. Boron
  256807. Prenyl Boronate
  256808. Indole
  256809. 22152N
  256810. 2/28/96V
  256811. Total Synthesis of GypsetinW
  256812. 1995X
  256813. 7025Y
  256814. GABRIEL WEATHERHEAD
  256815. Danishefsky, S. J.B
  256816. JACSC2Oxidative Cyclization
  256817. Dimethyldioxirane
  256818. AnnulationI
  256819. 22153N
  256820. 2/28/96V
  256821. Total Synthesis of GypsetinW
  256822. 1995X
  256823. 7025Y
  256824. GABRIEL WEATHERHEAD
  256825. A    Rieke, R.B
  256826. JACSC@Grignard 
  256827. Activated Magnesium
  256828. Diene
  256829. Cyclopropanol
  256830. Cyclopentenol
  256831. 22154N
  256832. 2/28/96
  256833. Reactions of Substituted (2-Butene-1,4-diyl)magnesium Complexes with Carboxylic Esters and Lactones:  Formation of a Versatile Intermediate Capable of Generating Substituted Cyclopentenols, Fused-Ring Cyclopentenols, or b,g-Unsaturated Ketones
  256834. 1995X
  256835. 5429Y
  256836. GABRIEL WEATHERHEAD
  256837. Grubbs, R. H.B
  256838. JACSC)Organoruthenium Transition Metal Complex
  256839. 22155N
  256840. 2/28/96
  256841. Reactions of Ruthenium Carbenes of the Type (PPh3)2(X)2Ru=CH-CH=CPh2 (X =Cl and CF3COO) with Strained Acyclic Olefins and Functionalized Olefins
  256842. 1995X
  256843. 5503Y
  256844. GABRIEL WEATHERHEAD
  256845. White, J. D.B
  256846. JACSC
  256847. Hydroboration
  256848. Suzuki Coupling
  256849. Palladium Catalyst
  256850. Boronic Ester
  256851. Negishi Carbozirconation
  256852. Chiral Allyl Boronate 
  256853. H. C. Brown Method
  256854. Charette Asymmetric Cyclopropanation
  256855. Organozinc
  256856. Wittig Reaction
  256857. 22156N
  256858. 2/28/96
  256859. AYSynthesis of Curacin A.  A Powerful Antimitotic from the Cyanobacterium Lyngbya majuscula
  256860. 1995X
  256861. 5612Y
  256862. GABRIEL WEATHERHEAD
  256863. Ichikawa, J.B
  256864. CKNazarov Cyclization
  256865. Annulation
  256866. TMSOTf Mediated Ring Closure
  256867. Organofluorine
  256868. K]Reviews:  Denmark, S. E. In Organic Reactions; Paquette, L. A. , Ed.; 1994; vol 45, pp 1-158.M
  256869. 22157N
  256870. 2/28/96VhFluorine-Directed Nazarov Cyclizations:  A Controlled Synthesis of Cross-Conjugated 2-Cyclopenten-1-onesW
  256871. 1995X
  256872. 2320Y
  256873. GABRIEL WEATHERHEAD
  256874. A    Piers, E.B
  256875. JOCCXVinyl Stannane
  256876. Organotin
  256877. Copper
  256878. Organocopper
  256879. 1,4-Addition Reaction
  256880. Annulation
  256881. EnoneI
  256882. 22158N
  256883. 2/28/96
  256884. Intramolecular Michael Additions:  Copper(I) Chloride-Mediated Conjugate Addition of Vinyltrimethylstannane Functions to a,b-Unsatutated Ketones
  256885. 1995X
  256886. 2322Y
  256887. GABRIEL WEATHERHEAD
  256888. Sulikowski, G. A.B
  256889. JOCCVChiral Nitrogen Ligand
  256890. Rhodium Carbene
  256891. Copper Carbene Complex
  256892. Asymmetric C-H InsertionI
  256893. kFirst enantioselective copper catalyzed C-H insertion.  Yields for the above reaction >85%.  The initital product of the C-H insertion was obtained as a mixture of four diastereomers.  The mixture about the C-9 (ester group) with a-H at C-9a provides product A after the DDQ oxidation, while product B is derived from the two compounds containing the b-H at C-9a.
  256894. 22159N
  256895. 2/28/96V
  256896. Enantioselective Synthesis of a 1,2-Disubstituted Mitosene by a Copper-Catalyzed Intramolecular Carbon-Hydrogen Insertion Reaction of a Diazo EsterW
  256897. 1995X
  256898. 2327Y
  256899. GABRIEL WEATHERHEAD
  256900. Ebert, G. W.B
  256901. JOCC;Organocopper Reagents
  256902. Activated Copper
  256903. Acylation
  256904. AlkylationI
  256905. ACPreparation of activated copper:  CuI
  256906. PEt3 + Li+[napth]*-  -->  Cu*
  256907. 22160N
  256908. 2/28/96VYDirect Formation of (Haloaryl)copper Nucleophiles from Haloiodobenzenes and Active CopperW
  256909. 1995X
  256910. 2361Y
  256911. GABRIEL WEATHERHEADw2Acid  Chloride ->Ketone
  256912. Haloarene -> Diarylketone 
  256913. Normant, J. F.B
  256914. JOCCWAllyl Zinc Reagent
  256915. Cyclopropane Synthesis
  256916. Organozinc
  256917. Cuprate
  256918. Lithium carbanion
  256919. GrignardI
  256920. Also see:  JOC 1994, 59, 4154
  256921. Reaction of the cyclopropyl zinc bromide with Me2Cu(CN)Li2 provides the corresponding cyclopropyl organocopper  reagent.  The bismetallic species is presumably dimeric in nature.
  256922. 22161N
  256923. 2/28/96VIStereodefined Substituted Cyclopropyl Zinc Reagents from Gem-BismetallicsW
  256924. 1995X
  256925. 2488Y
  256926. GABRIEL WEATHERHEAD
  256927. A    Padwa, A.B
  256928. CDSilylation
  256929. Lewis Acid
  256930. TMSOTf
  256931. [4+2] Annulation
  256932. Dipolar Cycloaddition
  256933. 22162N
  256934. 2/28/96VVA Novel Trimethylsilyl Triflate-Promoted Annulation of N-Acetoacetylated Alkenyl AmideW
  256935. 1995X
  256936. 2952Y
  256937. GABRIEL WEATHERHEAD
  256938. Wender, P. A.B
  256939. JOCCRNickel (0) Catalyzed Intramolecular [4+2] Cycloaddition
  256940. Diels-Alder 
  256941. Diene
  256942. Alkyne
  256943. 22163N
  256944. 2/28/96V
  256945. Transition Metal-Catalyzed Intramolecular [4+2] Cycloadditions:  Initial Studies on Stereochemistry and on Steroid and Vitamin D  Analog SythesesW
  256946. 1995X
  256947. 2962Y
  256948. GABRIEL WEATHERHEAD
  256949. Baker, D. C.B
  256950. JOCCmOrganoboron
  256951. Crotyldiisopinocampheylborane
  256952. Homoallylic Alcohol 
  256953. Oxy mercuration
  256954. Mercuric Acetate
  256955. HIV inhbitor
  256956. 22164N
  256957. 2/28/96V1Synthesis of Optically Active Calanolides A and BW
  256958. 1995X
  256959. 2964Y
  256960. GABRIEL WEATHERHEADw
  256961. Aldehyde -> Homoallylic alcohol
  256962. Charette, A. B.B
  256963. JOCC?Organozinc
  256964. Syn Cyclopropanation
  256965. Allylic Alcohol
  256966. Samarium 
  256967. ArDiastereoselectivity was found to be significantly higher utilizing the iodomethylzinc conitions vs Sm(Hg)/ CH2I2 
  256968. 22165N
  256969. 2/28/96VtDiastereoselective Cyclopropanation of Chiral Allylic Alcohols:  A More Efficient Reagent for Relative StereocontrolW
  256970. 1995X
  256971. 2966Y
  256972. GABRIEL WEATHERHEADw
  256973. Alkene -> Cyclopropane
  256974. Keck, G. E.B
  256975. JOCC+Samarium Iodide
  256976. Reduction
  256977. Alkene Synthesis
  256978. A7Deuterium incorporation is observed with CD3OD is used.
  256979. 22166N
  256980. 2/28/96VeUse of Samarium Diiodide as an alternative to Sodium/Mercury Amalgam in the Julia-Lythgoe OlefinationW
  256981. 1995X
  256982. 3194Y
  256983. GABRIEL WEATHERHEADw
  256984. Vinyl sulfone -> alkene / diene
  256985. Suzuki, K.B
  256986. TetrahedronC.Siloxyfuran Diels-Alder
  256987. Benzyne
  256988. CAN Oxidation
  256989. K,yield is after CAN oxidation to the quinone.
  256990. 22167N
  256991. 2/28/96V]Total Synthesis of Antibiotic C104:  Benzyne-Furan Cycloaddition Approach to the AngucyclinesW
  256992. 1995X
  256993. 7347Y
  256994. GABRIEL WEATHERHEAD
  256995. Suzuki, K.B
  256996. TetrahedronC-C-glycoside
  256997. Carbohydrate
  256998. Glycoside
  256999. Lewis AcidI
  257000. 22168N
  257001. 2/28/96V]Total Synthesis of Antibiotic C104:  Benzyne-Furan Cycloaddition Approach to the AngucyclinesW
  257002. 1995X
  257003. 7347Y
  257004. GABRIEL WEATHERHEAD
  257005. A    Sinay, P.B
  257006. J.C.S. Chem. Commun.C;Samarium Iodide
  257007. Ketyl radical
  257008. Aldol type ring closure
  257009. 22169N
  257010. 2/28/96V
  257011. Samarium (II) Iodide Promoted Ring Contraction of Carbohydrate Derivatives:  An Expeditious Synthesis of Functionalized CyclopentanesW
  257012. 1995X
  257013. 1373a
  257014. GABRIEL WEATHERHEAD
  257015. Hoffmann, H. M. R.B
  257016. TetrahedronC=Tandem Radical Cyclization
  257017. Carbohydrate Chemistry
  257018. Annulation
  257019. 22170N
  257020. 2/28/96V
  257021. Radical Cascades in Synthesis.  Dioxatrinanes and Doubly-Annulated Glycosides by Triethylborane Induced Atom-Transfer Cyclization of 1,5-Enynes and 1,5-DiynesW
  257022. 7389Y
  257023. GABRIEL WEATHERHEAD
  257024. A    Otera, J.B
  257025. JOCCcOrganolithium 
  257026. Lithium
  257027. Allylic Metalation
  257028. Conjugate Addition
  257029. Tin Enolate
  257030. Alkylation
  257031. NaIO4 OxidationI
  257032. KvOxidation of product shown with sodium metaperiodate affords the unsaturated aldehyde (via Evans-Mislow rearrangement)M
  257033. 22171N
  257034. 2/28/96
  257035. AkA Highly Practical Route for Prostaglandins by Conjugate Addition of a-Lithio-g-methoxyallyl Phenyl Sulfide
  257036. 1995X
  257037. 3936Y
  257038. GABRIEL WEATHERHEAD
  257039.  A    Otera, J.B
  257040. JOCCPZinc 
  257041. Organozinc
  257042. Chiral Titanium Catalyst
  257043. Seebach method
  257044. Tartarate / Ti(i-OPr)4 I
  257045. 22172N
  257046. 2/28/96
  257047. AkA Highly Practical Route for Prostaglandins by Conjugate Addition of a-Lithio-g-methoxyallyl Phenyl Sulfide
  257048. 1995X
  257049. 3936Y
  257050. GABRIEL WEATHERHEADw
  257051. Aldehyde -> Alcohol
  257052. !A    Padwa, A.B
  257053. A3a-thio-isobenzofuran
  257054. Diels-Alder
  257055. Pummerer Reaction
  257056. 22173N
  257057. 2/28/96ViA New Approach to the 1-Arylnaphthalene Lignans Utilizing a Tandem Pummerer-Diels-Alder Reaction SequenceW
  257058. 1995X
  257059. 3938Y
  257060. GABRIEL WEATHERHEAD
  257061. Sharpless, K. B.B
  257062. JOCC-Osmylation
  257063. Diol Synthesis
  257064. Chiral Ligand
  257065. 22174N
  257066. 2/28/96VXNew Ligands and Improved Enantioselectives for the Asymmetric Dihydroxylation of OlefinsW
  257067. 1995X
  257068. 3940Y
  257069. GABRIEL WEATHERHEADw
  257070. Alkene -> diol
  257071. Lautens, M.B
  257072. JOCC6Organostannane
  257073. Organolithium
  257074. Lithium
  257075. Electrophile
  257076. 22175N
  257077. 2/28/96VIStudies in the Transmetalation of Cyclopropyl, Vinyl, and Epoxy StannanesW
  257078. 1995X
  257079. 4213Y
  257080. GABRIEL WEATHERHEAD
  257081. Roush, W. R.B
  257082. Tet. Lett.CRLithium Enolate
  257083. Titanium Enolate
  257084. Boron Enolate
  257085. Matched Double Asymmetric InductionI
  257086. 22176
  257087. 2/28/96
  257088. A) Diastereoselective Aldol Reactions of Chiral Aldehydes and Chiral Methyl Ketones:  Dependence of Stereoselectivity on the Metal Enolate, the Aldehyde 2,3-Stereochemistry, and the Aldehyde b-Alkoxy Protecting Group 
  257089. B) Synthesis of the C(3)-C(15) Segment of Rutamycin B via a C(8)-C(9) Fragment Assembly Aldol Reaction:  Metal Dependence of the Aldehyde and Enolate Diastereofacial Selectivities
  257090. 1995X
  257091. 3443, 3447Y
  257092. GABRIEL WEATHERHEAD
  257093. Magnus, P.B
  257094. Tet. Lett.C
  257095. Intramolecular Pyrylium Ylide Cycloaddition
  257096. Annulation
  257097. Evans Chiral Auxiliary
  257098. Acylation of Enolate
  257099. Corey CBS Reduction
  257100. Cyclopropanation
  257101. Reductive ring expansionI
  257102. 22177N
  257103. 2/28/96V
  257104. New Strategy for the Synthesis of the Taxane Diterpenes:  Formation of the BC Rings of Taxol via [5+2]-Pyrylium Ylide-Alkene Cyclization, Ring Expansion StrategyW
  257105. 1995X
  257106. 5327Y
  257107. GABRIEL WEATHERHEAD
  257108. Magnus, P.B
  257109. Tet. Lett.C
  257110. Carboxylic Acid 
  257111. Enolate
  257112. Taxol
  257113. Ring Fragmentation
  257114. Transannular Hydride Migration
  257115. Oxidation 
  257116. Reduction
  257117. Cuprate
  257118. Enol Triflate
  257119. Conjugate Addition of Sulfone AnionI
  257120. 22178N
  257121. 2/28/96V|New Strategy for the Synthesis of the Taxane Diterpenes:  Formation of the A-Ring and Introduction of the C-1 Hydroxyl GroupW
  257122. 1995X
  257123. 5331Y
  257124. GABRIEL WEATHERHEAD
  257125. Magnus, P.B
  257126. Tet. Lett.C
  257127. Dieckmann
  257128. Claisen CondensationI
  257129. 22179N
  257130. 2/28/96V|New Strategy for the Synthesis of the Taxane Diterpenes:  Formation of the A-Ring and Introduction of the C-1 Hydroxyl GroupW
  257131. 1995X
  257132. 5331Y
  257133. GABRIEL WEATHERHEAD
  257134. Evans, D. A.B
  257135. Tet. Lett.CaMukaiyama Aldol Reaction
  257136. Nucleophile 
  257137. Carbonyl  Addition
  257138. Enolate
  257139. Asymmetric Reduction
  257140. Cram Model
  257141. HB = iPr2NEt
  257142. 22180N
  257143. 2/28/96
  257144. 1) 1,3-Asymmetric Induction in the Aldol Addition Reactions of Methyl Ketone Enolates and Enolsilanes to b-Substituted Aldehydes.  A Model for Chirality Transfer
  257145. 2) 1,3-Asymmetric Induction in Hydride Addition Reactions to b-Substituted Ketones.  A Model for Chirality Transfer
  257146. 1994X
  257147. 8537, 8541Y
  257148. GABRIEL WEATHERHEAD
  257149. Takeshi Oriyama
  257150. et al.B
  257151. Tet. Lett.C=acetal
  257152. furan
  257153. tin chloride
  257154. lewis acid
  257155. allylation
  257156. hydroxymethylI
  257157. 22181N
  257158. 2/28/96V
  257159. A Novel and Convenient Synthesis of 2-Aryl-4methylenetetrahydrofurans from 2-(Trimethylsiloxymethyl)allyltrimethylsilane and AcetalsW
  257160. 1995X
  257161. 5581Y
  257162. GABRIEL WEATHERHEADw
  257163. acetal -> furan
  257164. Chwang Siek Pak
  257165. et al.B
  257166. Tet. Lett.CVOlefination
  257167. reductive elimination
  257168. b-hydroxy sulfone
  257169. single electron transfer
  257170. magnesiumI
  257171. 22182N
  257172. 2/28/96
  257173. *V?An Efficient Julia Olefination Mediated by Magnesium in EthanolW
  257174. 1995X
  257175. 5607Y
  257176. GABRIEL WEATHERHEADw
  257177. hydroxy solfone -> alkeney
  257178. Korea IT
  257179. Ugo Azzena
  257180. et al.B
  257181. Tet. Lett.C?carbanions
  257182. wittig rearrangement
  257183. Metalation
  257184. lithiation
  257185. alkoxidesI
  257186. KLEX = MeI, (CH2CH2)O, (C6H5)2CO, D2O, C4H9Br
  257187. Yields generally >75% some >85%M
  257188. 22183N
  257189. 2/28/96VeMetalation of Arylmethyl Methyl Ethers and Connection with Their Reductive Electrophilic SubstitutionW
  257190. 1995X
  257191. 5641Y
  257192. lithiation - benzyl ethera
  257193. GABRIEL WEATHERHEADy
  257194. vienna
  257195. Shoji Kajigaeshi
  257196. et al.B
  257197. Bull. Chem. Soc. JpnC@aniline
  257198. halogentaion
  257199. iodination
  257200. diiodo
  257201. toluidines
  257202. xylidinesI
  257203. Kpthe presence of methanol greatly accelerates the reaction
  257204. less reactive nitroanilines were unsuccesfully reactedM
  257205. 22184N
  257206. 2/28/96V
  257207. Halogenation Using Quaternary Ammonium Polyhalides. VII. Iodination of Aromatic Amines by Use of Benzyltrimethylammonium Dichloroiodate(1-)W
  257208. 1988X
  257209. halogentaion - anilinesa
  257210. GABRIEL WEATHERHEAD
  257211. aniline -> iodoaniliney    Yokiwadai
  257212. Shoji Kajigaeshi
  257213. et al.B
  257214. Bull. Chem. Soc. JpnC
  257215. iodod
  257216. iodination
  257217. amideI
  257218. K7nitro- chloro- and bromo- acetanilides gave no reactionM
  257219. 22185N
  257220. 2/28/96V
  257221. Halogenation Using Quaternary Ammonium Polyhalides. XVII. Iodination of Acetanilide Derivatives with Benzyltrimethylammonium Dichloroiodate and Zinc ChlorideW
  257222. 1989X
  257223. 1349Y
  257224. halogenation - anilidesa
  257225. GABRIEL WEATHERHEADw
  257226. aryl amide -> iodoaryl amidey    Tokiwadai
  257227. Tsutomu Sugasawa
  257228. et al.B
  257229. JACSC_hydroxybenzylation
  257230. hydroxyalkylation
  257231. benzaldehydes
  257232. ortho acylation
  257233. nitriles
  257234. 2-aminobenzophenoneI
  257235. KUsolvent used is either dichloroethane or benzene
  257236. yields are generally better than 80%M
  257237. 22186N
  257238. 2/28/96VYAminohaloborane in Organic Synthesis. 1. Specific Ortho Substitution Reaction of AnilinesW
  257239. 1978X
  257240. 4842Y
  257241. boranes - anilinoboranesa
  257242. GABRIEL WEATHERHEADw
  257243. aldehyde -> benzyl alcoholy
  257244. Shionogi Labs
  257245. Japan
  257246. /A!William B. Lawson
  257247. Bernhard WitkopB
  257248. Tet. Lett.
  257249. indole
  257250. oxindole
  257251. indolone
  257252. Kjthe intermediate contains an aromatic bromine at the 5 position which is removed during the hydrogenolysisM
  257253. 22187N
  257254. 2/28/96V`A Simple Method for the Preparation of Oxindolacetic and Propionic Acids from the Parent Indoles\
  257255. heterocycle(N) - indolonea
  257256. GABRIEL WEATHERHEADw%indole -> oxindole
  257257. indole -> indoloney
  257258. A.I. Meyers
  257259. Masanao ShimanoB
  257260. JACSCcmetalation
  257261. regioselective
  257262. lithiation
  257263. directed
  257264. ortho
  257265. oxazoline
  257266. carboxamide
  257267. directing group
  257268. selectiveI
  257269. KGE = MeI, DMF, ClCO2Et, MeOD, 
  257270. EVL = ethoxyvinyllithium
  257271. >98% selectivityM
  257272. 22188N
  257273. 2/28/96VKEthoxyvinyllithium - HMPA. Surprising Regiochemistry in Aromatic MetalationW
  257274. 1994X
  257275. 10815Y
  257276. lithiation - orthoa
  257277. GABRIEL WEATHERHEADw
  257278. aryl -> aryllithiumy
  257279. Colorado State
  257280. 1A Michael C. Pirrung
  257281. Chiu-Yu HuangB
  257282. Tet. Lett.CIphotochemical
  257283. protecting group
  257284. alcohol
  257285. carbamates
  257286. amine
  257287. deprotectI
  257288. K yields range between 56% and 97%M
  257289. 22189N
  257290. 2/28/96
  257291. 1VcPhotochemical Deprotection of 3
  257292. -Dimethoxybenzoin (DMB) Carbamates Derived from Secondary AminesW
  257293. 1995X
  257294. 5883Y
  257295. protecting groups(N) - DMBa
  257296. GABRIEL WEATHERHEADw
  257297. carbamate -> aminey
  257298. Lutz F. Tietze
  257299. Thomas RaschkeB
  257300. Synlett.CGheck
  257301. palladium
  257302. BINAP
  257303. cyclization
  257304. chiral
  257305. ligand
  257306. allyl silane
  257307. aryl iodideI
  257308. 22190N
  257309. 2/28/96V
  257310. Enantioselective Total Synthesis of a Natural Noresquiterpene of the Calamenene Group by a Silane-Terminated Intramolecular Heck ReactionW
  257311. 1995X
  257312. palladium - Hecka
  257313. GABRIEL WEATHERHEAD
  257314. Joan Bosch
  257315. M.L. BennasarB
  257316. Synlett.CYdihydropyridine
  257317. cyclization
  257318. enolate
  257319. indoleacetic ester
  257320. tryptamine
  257321. strychnos
  257322. C-Mavacurine
  257323. 22191N
  257324. 2/28/96VzA General Method for the Synthesis of Bridged Indole Alkaloids. Addition of Carbon Nucleophiles to N-Alkylpyridinium SaltsW
  257325. 1995X
  257326. heterocycles(N) - indolea
  257327. GABRIEL WEATHERHEADy    Barcelona
  257328. 4A0William E. Parham
  257329. Lawrence D. Jones
  257330. Yoursy SayedB
  257331. 4CUmetalation
  257332. carboxylic acid
  257333. phenyl
  257334. propionic
  257335. acetic
  257336. halide
  257337. metal halogen exchangeI
  257338. reactions also done with m/p bromo phenylacetic acids.
  257339. Phenyl acetic acids give di and tri anions and reaction gives low yields of desired productM
  257340. 22192N
  257341. 2/28/96V
  257342. Selective Lithiation of Bromoarylalkanoic Acids and Amides at Low Temperature. Preparation of Substituted Arylalkanoic Acids and IndanonesW
  257343. 1975X
  257344. 2394Y
  257345. #16\ lithiation - arylalkanoinc acidsa
  257346. GABRIEL WEATHERHEADy
  257347. 5A"Fumie Sato
  257348. Yuan Gao
  257349. Kousuke HaradaB
  257350. Tet. Lett.Cotitanium isopropoxide
  257351. grignard
  257352. isopropyl magnesium bromide
  257353. hydrazone
  257354. aldimine
  257355. ketimine
  257356. metalloimine
  257357. allyl amineI
  257358. aR1 and R2 = Pr, Ph, Me, TMS, Hex  independently
  257359. R3 = Pr, C-hexyl, 2-furyl, Bu, Ph, Et, octyl
  257360. R4 = H, Me, Bu
  257361. R5 = Bn, Pr, Ph, OMe, Li, NMe2
  257362. Yields are generally better than 80% with the majority of cases leading to product 3 only with no trace of product 4
  257363. the reaction of imines is under more steric control than similar reactions of carbonyl compounds.
  257364. 22193N
  257365. 2/28/96VdStereoselective Synthesis of Allylic Amines by the Reaction of Titanium-Alkyne Complexes with IminesW
  257366. 1995X
  257367. 5913Y
  257368. GABRIEL WEATHERHEADw*alkyne -> allyl amine
  257369. imine -> allyl aminey
  257370. Tokyo Ins. Tec.
  257371. A.I. Meyers
  257372. James E. ResekB
  257373. Synlett.C
  257374. lactam
  257375. bicyclic
  257376. enantiomerI
  257377. 22194N
  257378. 2/28/96V
  257379. Intramolecular Photochemical [2+2] Cycloadditions of Enantiomerically Pure 4,4-Disubstituted Cyclohexenones: An Approach to the Total Asymmetric Synthesis of LintenoneW
  257380. 1995X
  257381. cyclization - 2+2 photoa
  257382. GABRIEL WEATHERHEADy
  257383. Colorado State
  257384. Oliver Reiser
  257385. Stephen HillersB
  257386. Synlett.
  257387. 7C}anti-aldol
  257388. ozonolysis
  257389. cross coupling
  257390. aryl halide
  257391. vinyl halide
  257392. palladium acetate
  257393. regioselective
  257394. trans selectivity
  257395. syn additionI
  257396. ratio of 2:4 is >98:2 in most cases. Hindered  o- substituted aryl iodides give 60:40. 
  257397. Reaction also done with iodo pyridines w/ high selectivity.
  257398. Yields are 48-70%M
  257399. 22195N
  257400. 2/28/96V
  257401. Palladium-Catalyzed Arylation and Vinylation of 4-Alkyl Substituted 2,3 -Dihydrofurans: A Catalytic Sequence to Anti-Aldol CompoundsW
  257402. 1995X
  257403. palladium - cross couplinga
  257404. GABRIEL WEATHERHEAD
  257405. 8A Thomas R. Bailey
  257406. Tandy L. DraperB
  257407. Synlett.CIpyridinepropenoic ethyl ester
  257408. ethyl acrylate
  257409. lithium chloride acceleratedI
  257410. R = H, 2-Me, or 3-Cl   also, a 2-NO2 6-Me compound
  257411. Yields generally better than 80% with NO2 case giving 40%
  257412. mixture of E and Z productsM
  257413. 22196N
  257414. 2/28/96V`Synthesis of 3-Pyridylpropenoic Acid Esters via Heck Coupling of Substituted 3-Pyridyl TriflatesW
  257415. 1995X
  257416. palladium - Hecka
  257417. GABRIEL WEATHERHEADw
  257418. triflate -> alkeney
  257419. Sanofi Winthrop Inc.
  257420. Masatomo Iwao
  257421. Osamu MotoiB
  257422. Tet. Lett.C
  257423. ergot alkaloid
  257424. indole
  257425. deprotection
  257426. 1,4 elimination
  257427. nucleophile
  257428. methiodide
  257429. N,N-dimethylamino
  257430. elimination addition
  257431. 3,4 disubstituted indoleI
  257432. KPNu = MeNO2, Phthalimide, TMS-CN, TMS-N3, HSPh, methyl acetate, dimethyl malonateM
  257433. 22197N
  257434. 2/28/96V
  257435. Methodology for the Efficient Synthesis of 3,4-Differentially Substituted Indoles. Fluoride Ion-Induced Elimination-Addition Reaction of 1-Triisopropylsilylgramine MethiodidesW
  257436. 1995X
  257437. 5929Y
  257438. Heterocycle(N) - Indolea
  257439. GABRIEL WEATHERHEADy
  257440. Nagasaki Univ.
  257441. D. Michael JonesB
  257442. JOCCttriflate
  257443. TBDMS
  257444. tert-butyl dimethylsilyl
  257445. hydroxyl
  257446. protection
  257447. protecting group
  257448. oxidation
  257449. carboxylic acid
  257450. benzylicKvcontains prep for using TBDMS triflate
  257451. RuO4 oxidation of benzylic position to carboxylic acid w/ removal of aryl groupM
  257452. 22198N
  257453. 2/28/96VIA Short Stereocontrolled Synthesis of Hydroxyethylene Dipeptide IsosteresW
  257454. 1993X
  257455. 2286Y
  257456. v.58\
  257457. protecting groups - TBDMSa
  257458. GABRIEL WEATHERHEAD
  257459. Munehiro NakataniB
  257460. Tet. Lett.C8Diels Alder
  257461. cycloaddition
  257462. electron defficient
  257463. dienophileI
  257464. KsBase = TEA in most cases
  257465. Yields are nearly quantitative in most cases
  257466. X = CO2Me
  257467. R1= H
  257468. R2= H or CO2Me
  257469. R3= H or CO2MeM
  257470. 22199N
  257471. 2/28/96V;A Base Catalyzed Diels-Alder Reaction of 3-Hydroxy-2-PyroneW
  257472. 1995X
  257473. 5939Y
  257474. Diels Aldera
  257475. GABRIEL WEATHERHEADy
  257476. Kagoshima Univ
  257477. Charles M. MarsonB
  257478. Tet. Lett.CYepoxidation
  257479. t-butyl hydroperoxide
  257480. SnCl4
  257481. tin chloride
  257482. hydroxy lactam
  257483. allylic alcohol
  257484. K?conditions = 2.2eq TBHP in DCM    2.2eq SnCl4 @ -78C for 1.5 hrM
  257485. 22200N
  257486. 2/28/96VaTin (IV)-Mediated Stereoselective Synthesis of Epoxides with Concomitant Alkyl Peroxide FormationW
  257487. 1995X
  257488. 5979Y
  257489. epoxidation - allylic alcohola
  257490. GABRIEL WEATHERHEAD
  257491. =A=Richard C. Storr
  257492. B.Kevin Park
  257493. Paul M. O
  257494. Lindsay A. WhiteB
  257495. Tet. Lett.M
  257496. 22201N
  257497. 2/28/96V+Quinoline Analogues of Ortho-QuinodimethaneW
  257498. 1995X
  257499. 5983Y
  257500. GABRIEL WEATHERHEADy    Liverpool
  257501. Buchwald, S. L.
  257502. Angew. Chem. Int. Ed. Engl. C7Palladium  
  257503. Organopalladium
  257504. Amine Synthesis
  257505. Annulation
  257506. KY10 examples of intermolecular Pd catalyzed coupling of aryl bromides with amines (67-89%)M
  257507. 22202N
  257508. 2/28/96VLA Simple Catalytic Method for the Conversion of Aryl Bromides to Aryl AminesW
  257509. 1995X
  257510. 1348Y
  257511. GABRIEL WEATHERHEADw
  257512. Aryl Bromide-> Aryl Amine
  257513. Takahashi, T.B
  257514. Angew. Chem. Int. Ed. Engl. CfEnediyne Antibiotics
  257515. Bergman cyclization
  257516. Diradical
  257517. 2,3-Wittig Rearrangement
  257518. Diels-Alder Cycloaddition
  257519. 22203N
  257520. 2/28/96VKSynthesis of a Dynamycin A Analogue and Its Bergman-Type CycloaromatizationW
  257521. 1995X
  257522. 1345Y
  257523. GABRIEL WEATHERHEAD
  257524. Takahashi, T.B
  257525. Angew. Chem. Int. Ed. Engl. CcPalladium Coupling
  257526. Annulation
  257527. Organostannane
  257528. Enediyne Antibiotic
  257529. Bergman Cyclization
  257530. Diradical
  257531. 22204N
  257532. 2/28/96VKSynthesis of a Dynamycin A Analogue and Its Bergman-Type CycloaromatizationW
  257533. 1995X
  257534. 1345Y
  257535. GABRIEL WEATHERHEAD
  257536. Tietze, L. F.
  257537. Angew. Chem. Int. Ed. Engl. C]Zirconium Cyclization
  257538. Organozirconium
  257539. Metalation
  257540. Lithium
  257541. Palladium Cyclization
  257542. Heck Reaction
  257543. 22205N
  257544. 2/28/96V
  257545. Efficient Total Synthesis of the Pharmacophore of the Anticancer Antiobiotic CC-1065 by Zirconocene and Palladium Initiated CyclizationsW
  257546. 1995X
  257547. 1366Y
  257548. GABRIEL WEATHERHEAD
  257549. Murphy, J. A.B
  257550. J.C.S. Chem. Commun.CJAnnulation
  257551. Radical Cyclization
  257552. Intramolecular
  257553. Azide Trap 
  257554. Amine Synthesis
  257555. AX95% yield after removal (treatment with water)  of the -Si(TMS)3 group (on the N atom). 
  257556. 22206N
  257557. 2/28/96V\Stereoselective Preparation of the ABCE Tetracycle of Aspidospermidine and Related AlkaloidsW
  257558. 1995X
  257559. 1409a
  257560. GABRIEL WEATHERHEAD
  257561. Hoveyda, A. H.B
  257562. JACSC3Organozirconium
  257563. Zirconium
  257564. Grignard
  257565. Organomagnesium
  257566. 22207N
  257567. 2/28/96
  257568. Enantio-, Diastereo-, and Regioselective Zirconium Catalyzed Carbomagnesation of Cyclic Ethers with Higher Alkyls of Magnesium.  Utility in Synthesis and Mechanistic ImplicationsW
  257569. 1995X
  257570. 7997Y
  257571. GABRIEL WEATHERHEAD
  257572. Trost, B. M.B
  257573. AwPalladium Chemistry
  257574. p-Allyl Pd Complex
  257575. Enolate Alkylation
  257576. Nucleophile
  257577. Chiral Ligand
  257578. Enantioselective C-C Bond Formation
  257579. 22208N
  257580. 2/28/96V3Asymmetric Alkylation of Allylic gem-DicarboxylatesW
  257581. 1995X
  257582. 7247Y
  257583. GABRIEL WEATHERHEAD
  257584. Trost, B. M.B
  257585. JACSC0Palladium Coupling
  257586. Annulation
  257587. Organotin Reagent
  257588. For synthesis of 5 5/2 mol% ratio of Pd(OAc)2 : TDMPP was used while 4 was formed when 3 mol% of each Pd(OAc)2 and TDMPP in the presence of tributyltin acetate which served as a transesterification catalyst
  257589. 22209N
  257590. 2/28/96VMDirecting Tandem Catalyzed Reactions as an Approach to Furans and ButenolidesW
  257591. 1995X
  257592. 7255Y
  257593. GABRIEL WEATHERHEAD
  257594. Hoveyda, A. H.B
  257595. APOrganonickel
  257596. Grignard Reagent
  257597. p-Allyl Nickel Complex
  257598. Carbomagnesation
  257599. Alkylation
  257600. 22210N
  257601. 2/28/96VjDirected Regio- and Stereoselective Nickel Catalyzed Addition of Alkyl Grignard Reagents to Allylic EthersW
  257602. 1995X
  257603. 7273Y
  257604. GABRIEL WEATHERHEAD
  257605. Paterson, I.B
  257606. SynlettC
  257607. Boron Enolate
  257608. Tin Enolate
  257609. Anti Aldol Condensation
  257610. Syn Aldol Reaction
  257611. Diastereoselective
  257612. Crotyl Chromium Reagent
  257613. Peterson Olefination
  257614. Stereoselective reduction
  257615. HydroborationI
  257616. 22211N
  257617. 2/28/96W
  257618. 1995X
  257619. GABRIEL WEATHERHEAD
  257620. Doyle, M. P.B
  257621. JACSCnrhodium carbene complex
  257622. Cyclopropane Synthesis
  257623. C-H Insertion
  257624. Annulation
  257625. Macrocyclic Intramolecular CyclizationI
  257626. 22212N
  257627. 2/28/96
  257628. HVpMacrocyclic Lactones from Dirhodium (II) Catalyzed Intramolecular Cyclopropanation and Carbon-Hydrogen InsertionW
  257629. 1995X
  257630. 7281Y
  257631. GABRIEL WEATHERHEAD
  257632. IA    Fu, G. C.B
  257633. JACSCITin Ketyl Radical
  257634. Tributyl Tin Hydride
  257635. Organotin
  257636. Stannane
  257637. Diol Synthesis
  257638. 22213N
  257639. 2/28/96VWMetal Hydride Mediated Intramolecular Pinacol Coupling of Dialdehydes and KetoaldehydesW
  257640. 1995X
  257641. 7283Y
  257642. GABRIEL WEATHERHEADw*Ketoaldehyde -> Diol
  257643. Dialdehyde -> Alcohol
  257644. Keck, G. E.B
  257645. JACSCWIntramolecular Aryl Lithium Ester Rearrangement 
  257646. Organolithium
  257647. Carbanion
  257648. TPAP OxidationI
  257649. 22214N
  257650. 2/28/96VKTotal Synthesis of (+)-Deoxypancratistatin:  A Radical Cyclization ApproachW
  257651. 1995X
  257652. 7289Y
  257653. GABRIEL WEATHERHEADw
  257654. Ester -> Ketone Alcohol
  257655. Keck, G. E.B
  257656. JACSCfRadical Oxime Cyclization
  257657. Annulation
  257658. Tributyl Tin Hydride
  257659. Organotin
  257660. Benzyl Radical
  257661. 6-Exo Cyclization
  257662. 22215N
  257663. 2/28/96VKTotal Synthesis of (+)-Deoxypancratistatin:  A Radical Cyclization ApproachW
  257664. 7289Y
  257665. GABRIEL WEATHERHEAD
  257666. Feldman, K. S.B
  257667. JACSC
  257668. Hypervalent Iodine
  257669. Organostannane
  257670. Alkynyliodonium Salt
  257671. Vinylidene Carbene
  257672. Annulation
  257673. Tosyl Enamine
  257674. Tandem Nucleophile / Carbene Insertion 
  257675. K(Proceeds through a carbene intermediate M
  257676. 22216N
  257677. 2/28/96V
  257678. Intramolecular Bicyclizations of Tosylamide-Containing Alkynyliodonium Salts as an Efficient Entry into Polycyclic Alkaloid SkeletaW
  257679. 1995X
  257680. 7544Y
  257681. GABRIEL WEATHERHEAD
  257682. Noyori, R.B
  257683. JACSChTransition Metal Transfer Hydrogenation
  257684. Aminosulfamide Ligand
  257685. Alcohol Synthesis
  257686. Organoruthenium Complex
  257687. 22217N
  257688. 2/28/96VbAsymmetric Transfer Hydrogenation of Aromatic Ketones Catalyzed by Chiral Ruthenium (II) ComplexesW
  257689. 1995X
  257690. 7562Y
  257691. GABRIEL WEATHERHEADw
  257692. Ketone -> Alcohol
  257693. Ogawa, O.
  257694. Sonoda, N.B
  257695. JACSC=Rhodium Complex
  257696. Organorhodium
  257697. Formylation
  257698. Acetylene
  257699. Aldehyde
  257700. 22218N
  257701. 2/28/96
  257702. NVvThe First Example of Transition Metal Catalyzed Thioformylation of Acetylenes with Aromatic Thiols and Carbon MonoxideW
  257703. 1995X
  257704. 7564Y
  257705. GABRIEL WEATHERHEAD
  257706. Myers, A. G.B
  257707. JACSCGEnediyne Antiobiotics
  257708. Antitumor Agent
  257709. Bergman Cyclization
  257710. DiradicalM
  257711. 22219N
  257712. 2/28/96V
  257713. Insights into the Mechanism of DNA Cleavage by Dynemicin A As Revealed by DNA Binding and Cleavage Studies of Synthetic AnalogsW
  257714. 1995X
  257715. 7574Y
  257716. GABRIEL WEATHERHEAD
  257717. Penner-Hahn, J. E.B
  257718. Copper
  257719. Higher order Cuprate
  257720. 22220N
  257721. 2/28/96V
  257722. Structural Characterization of Organocopper Complexes by EXAFS and XANES:  Evidence That Cyanide Does Not Coordinate to Cu in Dimethyl Cuprate SolutionsW
  257723. 1995X
  257724. 4310Y
  257725. GABRIEL WEATHERHEAD
  257726. Snyder, J. P.B
  257727. Copper
  257728. Higher order CuprateM
  257729. 22221N
  257730. 2/28/96V>Higher order Cyanocuprate Structure:  Cyanide Is Lithium BoundW
  257731. 1995X
  257732. 4312Y
  257733. GABRIEL WEATHERHEAD
  257734. Srebnik, M. B
  257735. RC,Organoboron
  257736. Boron
  257737. Zirconium Organozirconium
  257738. 22222N
  257739. 2/28/96VBFacile Boron Migration during Hydrozirconation of AlkenylborinatesW
  257740. 1995X
  257741. 4316Y
  257742. GABRIEL WEATHERHEAD
  257743. Rychnovsky, S. D.B
  257744. JOCC-Organoaluminum
  257745. Aluminum
  257746. Lewis Acid
  257747. Reduction
  257748. 22223N
  257749. 2/28/96VQA Mild Regioselective Ketal Claisen Rearrangement Promoted by TriisobutylaluminumW
  257750. 1995X
  257751. 4318Y
  257752. GABRIEL WEATHERHEAD
  257753. Shibasaki, M.B
  257754. JOCCjPalladium Coupling
  257755. Chiral Organopalladium
  257756. Aryl triflate
  257757. Steriod Skeleton
  257758. Intramolecular  Heck Cyclization
  257759. 95% eeM
  257760. 22224N
  257761. 2/28/96V
  257762. Regioselective Olefin Insertion in Asymmetric Heck Reaction.  Catalytic Asymmetric Synthesis of a Versitile Intermediate for Diterpene SynthesisW
  257763. 1995X
  257764. 4322Y
  257765. GABRIEL WEATHERHEAD
  257766. Tanaka, M.B
  257767. JOCC?Oxidative Coupling
  257768. Iron Perchlorate
  257769. ruthenium trifluoroacetate
  257770. 22225N
  257771. 2/28/96
  257772. Synthesis of Optically Pure Gosisin A:  The Total Synthesis of (+)-Schizandrin, (+)-Gomisin A, and (+)-Isoschizandrin in Naturally Occurring FormsW
  257773. 1995X
  257774. 4339Y
  257775. GABRIEL WEATHERHEAD
  257776. Roush, W. R.B
  257777. JOCC2Metal Halogen Exchange
  257778. Organolithium 
  257779. Aryl lithiumI
  257780. 22226N
  257781. 2/28/96V/Synthesis of Naphthoquinone Nucleus of AwamycinW
  257782. 1995X
  257783. 4412Y
  257784. GABRIEL WEATHERHEADw
  257785. Aryl Bromide -> Alcohol
  257786. Molander, G.B
  257787. JOCC8Annulation
  257788. Tin Fluoride
  257789. Ketoaldehyde
  257790. [3+5] CycloadditionI
  257791. dr = 7.5/1M
  257792. 22227N
  257793. 2/28/96VETotal Synthesis of (+)-Dactylol via a Novel [3+5] Annulation ApproachW
  257794. 1995X
  257795. 4559Y
  257796. GABRIEL WEATHERHEAD
  257797. Molander, G.B
  257798. Lewis Acid Catalyzed Michael Addition
  257799. Organotitanium Reagent
  257800. [3+5] Cycloaddition
  257801. Annulation
  257802. Decarboxylation
  257803. Tebbe Olefination
  257804. RhCl3 Mediated Alkene Isomerization
  257805. Lithium Reduction
  257806. 22228N
  257807. 2/28/96VETotal Synthesis of (+)-Dactylol via a Novel [3+5] Annulation ApproachW
  257808. 1995X
  257809. 4559Y
  257810. GABRIEL WEATHERHEAD
  257811. Posner, G. H.B
  257812. JOCCvLewis Acid
  257813. Zinc Bromide
  257814. Intramolecular Cycloaddition
  257815. Tandem Michael Addition Aldol Reaction
  257816. Silicon Tethered  D-A  RxnI
  257817. This reaction occurs by a stepwise mechanism to afford only  cis-exo and cis-endo adducts.  Control experiments demonstrated the stability of the E silyl enol ether to zinc bromide and the stability of the cycloadducts to the reaction conditions.  The Lewis acid, through coordination, must polarize the diene sufficiently to initiate nucleophilic attack by  the silyl enol ether.  This intermediate can then undergo isomerization and lose the stereochemical information originally contained inB
  257818.  the db of the enol ether.
  257819. 22229N
  257820. 2/28/96V
  257821. 2-Fluoroalkyl A-Ring Analogs of 1,25-Dihydroxyvitamin D3.  Stereocontrolled Total Synthesis via Intramolecular and Intermolecular Diels-Alder Cycloadditions.  Preliminary Biolgical TestingW
  257822. 1995X
  257823. 4617Y
  257824. GABRIEL WEATHERHEAD
  257825. ZA    Tsuji, Y.B
  257826. ZCjOrganostannane
  257827. Organosilicon
  257828. Palladium Catalyst
  257829. Allylsilane Synthesis
  257830. Tin reagent
  257831. Regioselective Coupling
  257832. 22230N
  257833. 2/28/96V^Stille Coupling Reaction Using 4-(Trimethylsilyl)-2-butenylstannanes to Afford Allylic SilanesW
  257834. 1995X
  257835. 4647Y
  257836. GABRIEL WEATHERHEAD
  257837. Rigby, J. H.B
  257838. JACSC]Palladium Cyclization
  257839. Endo selective cyclization
  257840. Annulation
  257841. Heck Reaction
  257842. Jeffery Conditions
  257843. 22231N
  257844. 2/28/96VGEndo-Selective Cyclization Pathways in the Intramolecular Heck ReactionW
  257845. 1995X
  257846. 7834Y
  257847. GABRIEL WEATHERHEAD
  257848. Danishefsky, S. J.B
  257849. JACSC^Glycoside Coupling
  257850. Carbohydrate Chemistry
  257851. Glycoconjugate
  257852. Oligosaccharide
  257853. Lewis Acid ConditionsI
  257854. 22232N
  257855. 2/28/96V:Total Synthesis of a Human Breast Tumor Associated AntigenW
  257856. 1995X
  257857. 7840Y
  257858. GABRIEL WEATHERHEAD
  257859. Lee, E.B
  257860. JACSC^Radical Ring Closure
  257861. Tin Hydride
  257862. Silicon Hydride
  257863. Peterson Olefination
  257864. (Trichloromethyl)lithiumI
  257865. 22233N
  257866. 2/28/96V
  257867. Total Synthesis of DactomelynesW
  257868. 1995X
  257869. 8017Y
  257870. GABRIEL WEATHERHEAD
  257871. Angle, S.R.B
  257872. JACSC2Tin Tetrachloride
  257873. Annulation
  257874. Roskamp Homologation
  257875. 22234N
  257876. 2/28/96
  257877. Stereoselective Synthesis of Tetrahydrofurans via the Lewis Acid Promoted Reaction of b-Benzyloxy Aldehydes and Ethyl Diazoacetate
  257878. 1995X
  257879. 8041Y
  257880. GABRIEL WEATHERHEAD
  257881. Aube, J.B
  257882. JACSCJNitrogen Ring Expansion 
  257883. Lewis Acid
  257884. Chiral Azido Alcohol
  257885. Lactam Synthesis
  257886. 22235N
  257887. 2/28/96VuEfficient Nitrogen Ring Expansion Process Facilitated by in Situ Hemiketal Formation.  An Asymmetric Schmidt ReactionW
  257888. 1995X
  257889. 8047Y
  257890. GABRIEL WEATHERHEAD
  257891. Townsend, C. A.B
  257892. JACSC+Enediyne Antibiotics
  257893. DNA Cleavage
  257894. DiradicalM
  257895. 22236N
  257896. 2/28/96V
  257897. Role of the Aryl Iodide in the Sequence-Selective Cleavage of DNA  by Calicheamicin.  Importance of Thermodynamic Binding vs Kinetic Activation in the Cleavage ProcessW
  257898. 1995X
  257899. 8074Y
  257900.  117Z
  257901. GABRIEL WEATHERHEAD
  257902. Kende, A.S.B
  257903. A.Lithium Enolate 
  257904. B-Lactam
  257905. Acylation Reduction
  257906. 22237N
  257907. 2/28/96VBTotal Synthesis of the Macrolide Antitumor Antibiotic Lankacidin CW
  257908. 1995X
  257909. 8258Y
  257910. GABRIEL WEATHERHEAD
  257911. Kende, A. S. B
  257912. JACSC
  257913. Stork Takahashi  Alkylation
  257914. Macrocylization
  257915. Lithium Anion 
  257916. Cyanohydrin Anion
  257917. Corey CBS Reduction
  257918. Palladium Coupling
  257919. Brown Crotyl Borane
  257920. Diisopinocampheylborane
  257921. Full PaperM
  257922. 22238N
  257923. 2/28/96VBTotal Synthesis of the Macrolide Antitumor Antibiotic Lankacidin CW
  257924. 1995X
  257925. 8258Y
  257926. GABRIEL WEATHERHEAD
  257927. Burk, M. J.B
  257928. JACSCGEnantioselective Hydrogenation
  257929. Cationic Rhodium Catalyst
  257930. Chiral Ligand
  257931. AIUsing supercritical CO2 as solvent up to 20% higher ee
  257932. s can be obtained.
  257933. 22239N
  257934. 2/28/96
  257935. cVLAsymmetric Catalytic Hydrogenation Reactions in Supercritical Carbon DioxideW
  257936. 1995X
  257937. 8277Y
  257938. GABRIEL WEATHERHEAD
  257939. Reich, H. J.B
  257940. JACSC%Organolithium 
  257941. Carbanion
  257942. Aggregation
  257943. 22240N
  257944. 2/28/96V7Solution Structure of Allenyl Propargyllithium ReagentsW
  257945. 1995X
  257946. 8470Y
  257947. GABRIEL WEATHERHEAD
  257948. Sulikowski, G. A.B
  257949. JACSC
  257950. Diels-Alder Cycloaddition
  257951. 22241N
  257952. 2/28/96VkTotal Synthesis of the Angucycline Antibiotics Urdamycinone B and 104-2 via a Common Synthetic IntermediateW
  257953. 1995X
  257954. 8472Y
  257955. GABRIEL WEATHERHEAD
  257956. Moore, H. W.B
  257957. JACSC:Annulation
  257958. Aldol Ring Closure
  257959. Vinyl Lithium
  257960. Organolithium
  257961. 22242N
  257962. 2/28/96VAA Tandem Oxy-Cope Transannular Ring Closure Route to PolyquinanesW
  257963. 1995X
  257964. 8486Y
  257965. GABRIEL WEATHERHEAD
  257966. Moore, H. W.B
  257967. JACSCAIntramolecular [2+2] Cycloaddtion
  257968. Ketene
  257969. Cyclobutenone
  257970. AnnulationI
  257971. 22243N
  257972. 2/28/96VAA Tandem Oxy-Cope Transannular Ring Closure Route to PolyquinanesW
  257973. 1995X
  257974. 8486Y
  257975. GABRIEL WEATHERHEAD
  257976. Myers, A. G.B
  257977. JACSCALithium Enolate
  257978. Alkylation
  257979. Chiral Auxiliary
  257980. Amino Acid Synthesis
  257981. At -78
  257982. C N,O dianion is formed which upon warming to 0
  257983. C equilibrates to the Z enolate by C to N proton transfer.  This method (above scheme) has been applied to the antitumor compound kedarcidin.M
  257984. 22244N
  257985. 2/28/96
  257986. AzA Practical Method for the Synthesis of D- or L-a-Amino Acids by the Alkylation of (+)- or (-)-Pseudoephedrine Glycinamide
  257987. 1995X
  257988. 8488Y
  257989. GABRIEL WEATHERHEAD
  257990. Kang, S-K.B
  257991. JOCCLOxidation
  257992. Palladium (II) Catalyst
  257993. Copper Chloride
  257994. Anti Markovnikov Addition
  257995. The diol corresponding to the above substates provides a 90% yield of the methyl  ketone (the expected Markovnikov addtion to the alkene)M
  257996. 22245N
  257997. 2/28/96VhComplete Reverse Regioselection in Wacker Oxidation of Acetonides and Cyclic Carbonates of Allylic DiolsW
  257998. 1995X
  257999. 4678Y
  258000. GABRIEL WEATHERHEADwDalkene  -> aldehyde
  258001. alkene ->unsaturated aldehyde
  258002. alkene  -> ketone 
  258003. Ito, Y
  258004. Ogawa, T.B
  258005. JOCCIGlycoside Coupling
  258006. DDQ Oxidation
  258007. Carbohydrate Chemistry
  258008. Oligosaccharide
  258009. KGIntramolecular coupling using a stereocontrolling linking functionalityM
  258010. 22246N
  258011. 2/28/96VzA Convergent and Stereocontrolled Synthetic Route to the Core Pentasaccharide Structure of Asparagine Linked GlycoproteinsW
  258012. 1995X
  258013. 4680Y
  258014. GABRIEL WEATHERHEAD
  258015. Brown, H. C.B
  258016. JOCCxOrganoboron Reagent
  258017. Allenylboronate
  258018. Hydroboration
  258019. Chiral Diol Synthesis
  258020. Allylic Alcohol 
  258021. Homoallylic Alcohol
  258022. Oxidation
  258023. 22247N
  258024. 2/28/96
  258025. [(E)-g-(1,3,2)-Dioxaborinanyl)allyl]diisopinocampheylborane, an Exceptional Reagent for the Stereo- and Enantioselective Synthesis of anti-1-Alkene-3,4-diols via a Masked a-Hydroxyallylboration
  258026. 1995X
  258027. 4686Y
  258028. GABRIEL WEATHERHEADw
  258029. aldehyde -> alcohol
  258030. Haynes, R. K.B
  258031. JOCCNMichael Addition 
  258032. Conjugate Addition
  258033. Organolithium Enolate
  258034. Amide Li Dienolate
  258035. 22248N
  258036. 2/28/96VoDiastereo- and Regioselectivity in the Reactions of Dilithiated Allylic Secondary Amides with Cyclopent-2-enoneW
  258037. 1995X
  258038. 4690Y
  258039. GABRIEL WEATHERHEAD
  258040. Enholm, E. J.B
  258041. JOCCeRadical Cyclization
  258042. Annulation
  258043. Tributyltin Hydride
  258044. Organotin
  258045. Tin Enolate
  258046. Stannane
  258047. Aldol Condensation
  258048. 22249N
  258049. 2/28/96V1Cyclization Reactions of Allylic O-Stannyl KetylsW
  258050. 1995X
  258051. 4850Y
  258052. GABRIEL WEATHERHEAD
  258053. Ruzziconi, R.B
  258054. JOCCBCAN Oxidation
  258055. Diene
  258056. Palladium Coupling 
  258057. Alkylation
  258058. Radical Cation
  258059. 22250N
  258060. 2/28/96V
  258061. Regio- and Stereoselective Synthesis of Unsaturated Carbonyl Compounds Based on Ceric Ammonium Nitrate Promoted Oxidative Addition of Trimethylsilyl Enol Ethers to Conjugated DienesW
  258062. 1995X
  258063. 4954Y
  258064. GABRIEL WEATHERHEAD
  258065. Pearson, W. H.
  258066. JOCCPRearrangement
  258067. Nitrogen Ring Expansion 
  258068. Carbocation
  258069. Sodium Borohydride Reduction
  258070. 22251N
  258071. 2/28/96V`Synthesis of Amines by the Intermolecular Schmidt Reaction of Aliphatic Azides with CarbocationsW
  258072. 1995X
  258073. 4960Y
  258074. GABRIEL WEATHERHEADw
  258075. alcohol -> amine
  258076. Aggarwal, V.B
  258077. JOCCKDiels-Alder Cycloaddition
  258078. Asymmetric DA Rxn
  258079. Sufoxide Dienophile
  258080. Lewis Acid
  258081. The bis-sulfoxide auxiliary can be removed in a two step sequence to afford the ketone in enantiomerically pure form and in high chemical yield. (81% overall)
  258082. The dieneophile was prepared in four steps featuring an asymmetric oxidation using DET andTi(Oi-Pr)4.(98% ee)
  258083. 22252N
  258084. 2/28/96Vq(1R, 3R)-2-Methylene-1,3-dithiolane 1,3-Dioxide:  A Highly Reactive and Highly Selective Chiral Ketene EquivalentW
  258085. 1995X
  258086. 4962Y
  258087. GABRIEL WEATHERHEAD
  258088. Ishii, Y. B
  258089. qC7Samarium Catalyst
  258090. Evans Tishchenko Rxn
  258091. Sm Ketyl RadicalI
  258092. The mechanism may involve an 8 membered cyclic intermediate.  Intramolecular hydride shift then produces the observed product and regenerates the catalyst.M
  258093. 22253N
  258094. 2/28/96V\A New Coupling Reaction of Vinyl Esters with Aldehydes Catalyzed by Organosamarium CompoundsW
  258095. 1995X
  258096. 4974Y
  258097. GABRIEL WEATHERHEAD
  258098. Shapiro, G.B
  258099. JOCC|Michael Addition
  258100. Conjugate Addition
  258101. Schollkopf Chiral Auxiliary
  258102. Vinyl Sulfone
  258103. Alkylation
  258104. Sulfone Carbanion
  258105. Lithium Enolate
  258106. Alkylation of the sulfone anion was attempted in one case with MeI as the alkylating agent.  With the Z-vinyl sulfone the major product had reversed configuration at the b-stereocentre (ie. the minor isomer has the structure shown above)
  258107. 22254N
  258108. 2/28/96
  258109. A<A Versatile Asymmetric Synthesis of b-Branched a-Amino Acids
  258110. 1995X
  258111. 4978Y
  258112. GABRIEL WEATHERHEAD
  258113. Turos, E. B
  258114. Electrophilic Ring Closure
  258115. Acetylene Iodocyclization
  258116. Iodine
  258117. [2+2] Cycloaddition
  258118. mCPBA Oxidation
  258119. Grignard Addition
  258120. Chelation Control
  258121. 22255N
  258122. 2/28/96
  258123. A/Synthesis of Inversely-Fused Bicyclic b-Lactams
  258124. 1995X
  258125. 4980Y
  258126. GABRIEL WEATHERHEAD
  258127. Feldman, K. S.B
  258128. JOCCJDiaryl Ether Synthesis
  258129. Grignard Reagent
  258130. Organocerium Reagent
  258131. Organocopper
  258132. "KkR = Me
  258133. Alternative to the Ullmann coupling reaction.  Organocopper and Grignard reagents were also studied.M
  258134. 22256N
  258135. 2/28/96VHChemistry of Galloyl-Derived o-Quinones:  Reactivity toward Nucleophilesa
  258136. GABRIEL WEATHERHEAD
  258137. Dorow, R. L.B
  258138. JOCC9Reductive Alkylation
  258139. Dimethylbromoborane
  258140. Azide Reduction
  258141. Both starting material and product enantiomeric purities were measured by chiral HPLC (99% ee).  Amides, acids and ethers were found to be stable to the reaction conditions.M
  258142. 22257N
  258143. 2/28/96
  258144. A6A Novel Preparation of Scalemic N-Methyl-a-amino Acids
  258145. 1995X
  258146. 4986Y
  258147. GABRIEL WEATHERHEADw
  258148. azide -> amine
  258149. Nicolaou, K. C.B
  258150. Chem. Eur. J.COOrganostannane
  258151. Palladium Coupling
  258152. Stille Coupling
  258153. Vinyl Iodide
  258154. Distannylethene
  258155. ADConditions: Pd(MeCN)2Cl2 (20 mol%), DMF-THF, EtNi-Pr2, RT
  258156. Full Paper
  258157. 22258N
  258158. 2/28/96V
  258159. Total Synthesis of RapamycinW
  258160. 1995X
  258161. GABRIEL WEATHERHEAD
  258162. Oikawa, H.
  258163. Ichihara, A.B
  258164. wCUSpiroketal
  258165. Reduction
  258166. Triethylsilane
  258167. Tin tetrachloride
  258168. Oxonium Ion
  258169. Bidentate ChelationI
  258170. 22259N
  258171. 2/28/96V
  258172. Total Synthesis of TautomycinW
  258173. 1995X
  258174. 5048Y
  258175. GABRIEL WEATHERHEAD
  258176. Oikawa, H.
  258177. Ichihara, A.B
  258178. Aldol Coupling Reaction
  258179. Anti-Felkin Adduct
  258180. Mukaiyama Aldol
  258181. Silyl Enol Ether
  258182. Lewis Acid
  258183. Titanium Tetrachloride
  258184. Trimethylsilyl triflateI
  258185. 22260N
  258186. 2/28/96V
  258187. Total Synthesis of TautomycinW
  258188. 1995X
  258189. 5048Y
  258190. GABRIEL WEATHERHEAD
  258191. Wiemer, D. F.
  258192. Scott, W. J.B
  258193. JOCCUStereoselective
  258194. Hydroxyl Directed
  258195. Hydrogenation
  258196. Iridium Complex
  258197. Crabtree
  258198. s Catalyst
  258199. 22261N
  258200. 2/28/96VsApplication of the Nickel Mediated Neopentyl Coupling in the Total Synthesis of the Marine Natural Product ArenarolW
  258201. 1995X
  258202. 5102Y
  258203. GABRIEL WEATHERHEAD
  258204. Wiemer, D. F.
  258205. Scott, W. J.B
  258206. JOCCHOrganonickel Coupling
  258207. Grignard Reagent
  258208. CAN Oxidation
  258209. Nysted Olefination
  258210. A\Nysted Conditions:  Zn(CH2ZnBr)2
  258211. THF, TiCl4 
  258212. (for installing an exo methylene from a ketone)
  258213. 22262N
  258214. 2/28/96VsApplication of the Nickel Mediated Neopentyl Coupling in the Total Synthesis of the Marine Natural Product ArenarolW
  258215. 1995X
  258216. 5102Y
  258217. GABRIEL WEATHERHEAD
  258218. Rieke, R. D.B
  258219. JOCCNOrganomagnesium 
  258220. Activated Magnesium
  258221. Diene
  258222. Epoxide
  258223. Lactone Synthesis
  258224. Rieke Mg
  258225. 22263N
  258226. 2/28/96
  258227. AjDirect Synthesis of Spiro g-Lactones, and Alcohols from Substituted (2-Butene-1,4-diyl)magnesium Complexes
  258228. 1995X
  258229. 5143Y
  258230. GABRIEL WEATHERHEAD
  258231. Weinreb, S. M.B
  258232. JOCC{Organosilane
  258233. Silylcuprate
  258234. Lewis Acid
  258235. Tin Tetrachloride
  258236. Annulation
  258237. Amine Synthesis
  258238. Imino Ene Reaction
  258239. Titanium TetrachlorideI
  258240. 22264N
  258241. 2/28/96V4Novel Intramolecular Ene Reactions of AllenylsilanesW
  258242. 1995X
  258243. 5366Y
  258244. GABRIEL WEATHERHEAD
  258245. Harada, T. B
  258246. JOCC4Organozinc
  258247. Methylenecyclopropane
  258248. Palladium Coupling
  258249. Reaction of the methylenecyclopropylalkylzinc reagent couples with a variety of electrophiles including TsCN, aldehyes, acid chlorides and ClCOOEt with Pd(0) catalysis, iodine and TMSCl.M
  258250. 22265N
  258251. 2/28/96V{Preparation of (1-Cyclopropylidenealkyl)-zinc Reagents by the Reaction of Homopropargylic Sulfonates with TriorganozincatesW
  258252. 1995X
  258253. 5370Y
  258254. GABRIEL WEATHERHEAD
  258255. Snider, B. B.B
  258256. JOCCRRadical Cyclization
  258257. Annulation
  258258. Manganese(III) acetate
  258259. Copper(II) acetate
  258260. OxidationI
  258261. 22266N
  258262. 2/28/96VHMn (III) Based Oxidative Free Radical Cyclization of Unsaturated KetonesW
  258263. 1995a
  258264. GABRIEL WEATHERHEAD
  258265. Jacobsen, E. N. B
  258266. JOCC.Epoxidation
  258267. Manganese Salen Complex
  258268. mCPBA
  258269. 22267N
  258270. 2/28/96VdKinetic Resolution of Racemic Chromenes via Asymmetric Epoxidation:  Synthesis of (+)-Teretifoline BW
  258271. 1995X
  258272. 5380Y
  258273. GABRIEL WEATHERHEAD
  258274. Kishi, Y. B
  258275. JOCCoKishi Nozaki Hiyama Rxn
  258276. Organochromium 
  258277. Organonickel
  258278. Chromium Chloride
  258279. Nickel Chloride
  258280. Chiral Dipyridyl Ligand
  258281. 22268N
  258282. 2/28/96V@Ni(II)/Cr(II) Mediated Coupling Reaction:  An Asymmetric ProcessW
  258283. 1995X
  258284. 5386Y
  258285. GABRIEL WEATHERHEADw9vinyl iodide  -> allylic alcohol
  258286. allyl bromide -> alcohol
  258287. A    Taber, D.B
  258288. JOCC2[4+2] D-A Cycloaddition
  258289. Silyl Baeyer-Villiger Rxn
  258290. 22269N
  258291. 2/28/96
  258292. AuPhenyldimethylsilyl as an Alcohol Surrogate in Intramolecular Diels-Alder Cycloaddition:  Synthesis of a-Dictyopterol
  258293. 1995X
  258294. 5537Y
  258295. GABRIEL WEATHERHEAD
  258296. Marshall, J. A.B
  258297. Organostannane
  258298. Allenyltin Reagent
  258299. BuSnCl3
  258300. Silver nitrate
  258301. Dess-Martin Oxidation
  258302. Stannyl Cuprate Addition
  258303. [2,3]-Wittig Rearrangement
  258304. Dihydropyran Synthesis
  258305. 22270N
  258306. 2/28/96
  258307. 1) Diastereo- and Enantioselective Synthesis of Allenylcarbinols through SE2
  258308.  Addition of Transient Nonracemic Propargylic Stannanes to Aldehydes
  258309. 2) Synthesis of syn,syn; anti,syn; anti,anti  Stereotriads from a Single Pair of Enantiomeric Reagents
  258310. 1995X
  258311. 5550, 5556Y
  258312. GABRIEL WEATHERHEAD
  258313. A    Cohen, T.B
  258314. JACSC
  258315. Thermal rearrangement
  258316. Biradical Intermediate
  258317. Annulation
  258318. Cyclopentene Synthesis
  258319. LDBB 
  258320. Reductive Lithiation
  258321. Lithiosilane
  258322. Potassium Hydride
  258323. Peterson Olefination
  258324. A$LDBB:  4,4
  258325. -di-tert-butylbiphenylide
  258326. 22271N
  258327. 2/28/96VaTheory and Mechanism of the Allylidenecyclopropane to Methylenecyclopentene Thermal IsomerizationW
  258328. 1995X
  258329. 8495Y
  258330. GABRIEL WEATHERHEAD
  258331. Norton, J. R.B
  258332. C@Organopalladium
  258333. Phosphine Ligand
  258334. Suzuki Coupling
  258335. Stille CouplingM
  258336. 22272N
  258337. 2/28/96VoMethyl/Phenyl Exchange between Palladium and a Phosphine Ligand.  Consequences for Catalytic Coupling ReactionsW
  258338. 1995X
  258339. 8576Y
  258340. GABRIEL WEATHERHEAD
  258341. Normant, J-F.B
  258342. JACSCKBenzylic Organolithium
  258343. Butyllithium
  258344. Sparteine
  258345. Alkylation
  258346. Chiral Carbanion
  258347. 22273N
  258348. 2/28/96VSAsymmetric Carbolithiation of Cinnamyl Derivatives in the Presence of (-)-SparteineW
  258349. 1995X
  258350. 8853Y
  258351. GABRIEL WEATHERHEAD
  258352. Hirama, M.B
  258353. JACSC,Enediyne Antibiotics
  258354. DNA Cleavage
  258355. Biradical
  258356. AsAlso see next paper:  JACS  1995, 117 (34), 8877  
  258357. The Benzoxazolinate of C-1027 Confers Intercalative DNA Binding
  258358. 22274N
  258359. 2/28/96
  258360. Synthesis and Characterization of Nine-Membered Cyclic Enediynes, Models of C-1027 and Kedarcidin Chromophore:  Equilibration with a p-Benzyne Biradical and Kinetic Stabilization
  258361. 1995X
  258362. 8875Y
  258363. GABRIEL WEATHERHEAD
  258364. Nugent, W. A.B
  258365. JACSC4Organotungsten Complex
  258366. Alkene Metathesis
  258367. Annulation
  258368. 22275N
  258369. 2/28/96VbPractical Catalyst for Cyclic Metathesis.  Synthesis of Functional and/or Enantiopure CycloalkenesW
  258370. 1995X
  258371. 8992Y
  258372. GABRIEL WEATHERHEADw
  258373. Diene -> Alkene
  258374. Schreiber, S. L.B
  258375. JACSC
  258376. Natural ProductI
  258377. 22276N
  258378. 2/28/96VNEnantiospecific Total Synthesis of the Protein Phosphatase Inhibitor MotuporinW
  258379. 1995X
  258380. 9069Y
  258381. GABRIEL WEATHERHEAD
  258382. Evans, D. A.B
  258383. JACSCsBoron Enolate
  258384. Titanium Enolate
  258385. Aldol Condensation
  258386. Felkin Control
  258387. Enolate Face Selectivity
  258388. Aldehyde Face SelectivityI
  258389. Fully , partially and mis-matched double stereodifferentiating reactions of chiral enolates (E-boron and Z-titanium) and chiral aldehydes.M
  258390. 22277N
  258391. 2/28/96V
  258392. Double Stereodifferentiating Aldol Reactions.  The Documentation of 
  258393. Partially Matched
  258394.  Aldol Bond Constructions in the Assemblage of Polypropionate SystemsW
  258395. 1995X
  258396. 9073Y
  258397. GABRIEL WEATHERHEADw
  258398. Aldehyde -> Alcohol
  258399. Evans, D. A.B
  258400. JACSC}Chiral Organolithium
  258401. Carbanion
  258402. Copper (II) pivalate
  258403. Oxidative Coupling
  258404. Sparteine
  258405. Chiral Base
  258406. Metalation
  258407. Phophine-borane
  258408. 22278N
  258409. 2/28/96VnEnantioselective Deprotonation as a Vehicle for the Asymmetric Synthesis of C2-Symmetric P-Chiral DiphosphinesW
  258410. 1995X
  258411. 9075Y
  258412. GABRIEL WEATHERHEAD
  258413. Yamamoto, H.B
  258414. JACSC`ATPH
  258415. Organoaluminum complex
  258416. Methyl Lithium
  258417. Organolithium
  258418. Aromatic Conjugate Addn
  258419. Methyl triflateI
  258420. 22279N
  258421. 2/28/96
  258422. Unprecidented Nucleophilic Addition of Organolithiums to Aromatic Aldehydes and Ketones by Complexation with Aluminum Tris(2,6-diphenylphenoxide)W
  258423. 1995X
  258424. 9091Y
  258425. GABRIEL WEATHERHEAD
  258426. Hayashi, T.B
  258427. JACSCHPalladium Coupling
  258428. Grignard Reagent
  258429. Aryl Triflate
  258430. Chiral Phophine LigandI
  258431. A313% of the bis arylation product (3a) was isolated.
  258432. 22280N
  258433. 2/28/96VxCatalytic Asymmetric Synthesis of Axially Chiral Biaryls by Palladium-Catalyzed Enantioposition-Selective Cross-CouplingW
  258434. 1995X
  258435. 9101Y
  258436. GABRIEL WEATHERHEAD
  258437. Yamamoto, H. B
  258438. SynlettC
  258439. Organoaluminum
  258440. Aluminum Reagent
  258441. Lewis Acid
  258442. Conjugate Addition
  258443. 1,4-Addition
  258444. Michael Addition
  258445. Organometallic
  258446. Nucleophile
  258447. Carbonyl Addition
  258448. 1,2-Addition
  258449. 22281N
  258450. 2/28/96V_Evaluation of Aluminum Tris(2,6-di-tert-butyl-4-methylphenoxide) (ATD) as a Lewis Acid ReceptorW
  258451. 1995X
  258452. GABRIEL WEATHERHEAD
  258453. w6acetylenic ketone -> alcohol
  258454. acetylenic ketone-> enone
  258455. Yamamoto, H. B
  258456. SynlettCKOrganoboron Lewis Acid
  258457. Boron Reagent
  258458. Epoxide Rearrangement
  258459. Alkyl migration
  258460. 22282N
  258461. 2/28/96VfTris(pentafluorophenyl)boron as an Efficient Catalyst in the Stereoselective Rearrangement of EpoxidesW
  258462. 1995X
  258463. GABRIEL WEATHERHEADw
  258464. epoxide -> aldehyde
  258465. Matsuda, F.B
  258466. SynlettC=SmI2
  258467. Samarium Ketyl Radical
  258468. Electron Transfer
  258469. Acrylonitrile 
  258470. 22283N
  258471. 2/28/96
  258472. AlSamarium (II) Iodide Mediated Intermolecular Ketone-Oefin Couplings Chelation Controlled by b-Hyroxyl Groups
  258473. 1995X
  258474. GABRIEL WEATHERHEADw
  258475. ketone -> alcohol 
  258476. Anderson, J. C.B
  258477. SynlettC^Boronic Acid
  258478. Organopalladium 
  258479. Palladium Complex 
  258480. Pd (PPh3)4
  258481. Thallium Hydroxide
  258482. Suzuki CouplingI
  258483. 22284N
  258484. 2/28/96VKAmbient Temperature Unsymmetrical Biaryl Synthesis Using Suzuki MethodologyW
  258485. 1995X
  258486. GABRIEL WEATHERHEAD
  258487. Nishizawa, M.B
  258488. SynlettCJOrganomercury
  258489. Mercury (II) Triflate
  258490. Olefin Cyclization
  258491. Glycoside Coupling
  258492. 22285N
  258493. 2/28/96VTNovel Synthetic Approaches into Intensely Sweet Gylcosides:  Baiyunoside and OsladinW
  258494. 1995X
  258495. GABRIEL WEATHERHEAD
  258496. Yamamoto, H.B
  258497. SynlettCMChiral Alkylation
  258498. Allyl Magnesium Reagent
  258499. Organomagnesium
  258500. Quaternary Carbon 
  258501. 22286N
  258502. 2/28/96
  258503. ARAsymmetric g-Methylation of Allylic Grignard Reagents Using a Chiral Leaving Group
  258504. 1995X
  258505. GABRIEL WEATHERHEAD
  258506. Dauben, W. G.B
  258507. SynlettC5Rhodium Carbene
  258508. C-H Insertion
  258509. Diazoketone
  258510. Diazoester
  258511. 22287N
  258512. 2/28/96
  258513. AbEnantioselective Synthesis of a Bicyclo[3.1.0]hexane A-Ring Synthon for 1a, 25-Dihydroxyvitamin D3
  258514. 1995X
  258515. GABRIEL WEATHERHEAD
  258516. Enders, D. B
  258517. SynlettC7Lithium Carbanion
  258518. Wittig Rearrangement
  258519. Hydrazone Anion
  258520. AK,95% syn,  high asymmetric induction (91% de)M
  258521. 22288N
  258522. 2/28/96V
  258523. Diastereo- and Enantioselective Synthesis of (-)-Oudemansin A via [2,3]-Wittig Rearrangement of Crotyloxyacetaldehyde-SAEP-HydrazoneW
  258524. 1995X
  258525. GABRIEL WEATHERHEAD
  258526. Berrisford, D. J.
  258527. Bolm, C.B
  258528. Angew. Chem. Int. Ed. Engl. C?Organotitanium Reagent
  258529. Chiral Catalyst
  258530. Organoaluminum Catalyst
  258531. BK+Recent developements
  258532.  0.5 mol% (R)-catalystM
  258533. 22289N
  258534. 2/28/96V+Catalytic Asymmetric Carbonyl Ene ReactionsW
  258535. 1995X
  258536. 1717Y
  258537. GABRIEL WEATHERHEAD
  258538. Danishefsky, S. J.B
  258539. Angew. Chem. Int. Ed. Engl. C1Benzyne
  258540. Lithium Carbanion
  258541. Dimethylmalonate
  258542. 22290N
  258543. 2/28/96V"Total Synthesis of (
  258544. )-Dynemycin AW
  258545. 1995X
  258546. 1721Y
  258547. GABRIEL WEATHERHEAD
  258548. Danishefsky, S. J.B
  258549. Angew. Chem. Int. Ed. Engl. CUAnnulation
  258550. Lithium Carbanion
  258551. Enolate
  258552. Phenyl iodondium bis(trifluoroacetate) Oxidation
  258553. 22291N
  258554. 2/28/96V"Total Synthesis of (
  258555. )-Dynemycin AW
  258556. 1995X
  258557. 1721Y
  258558. GABRIEL WEATHERHEAD
  258559. Danishefsky, S. J.B
  258560. Angew. Chem. Int. Ed. Engl. CFMetal Halogen Exchange
  258561. Vinyl Lithium  Reagent
  258562. 1,2-Addition to AldehydeI
  258563. EK/first step:  93% yield 
  258564. second step:  80% yieldM
  258565. 22292N
  258566. 2/28/96V
  258567. A Total Synthesis of TaxolW
  258568. 1995X
  258569. 1723Y
  258570. GABRIEL WEATHERHEADw
  258571. aldehyde -> alcohol
  258572. Danishefsky, S. J.B
  258573. Angew. Chem. Int. Ed. Engl. CQPalladium Acetate
  258574. Organopalladium
  258575. Heck Cyclization
  258576. Vinyl Triflate
  258577. Diene SynthesisI
  258578. 22293N
  258579. 2/28/96V
  258580. A Total Synthesis of TaxolW
  258581. 1995X
  258582. 1723Y
  258583. GABRIEL WEATHERHEAD
  258584. Buchwald, S. L. B
  258585. Angew. Chem. Int. Ed. Engl. C<Hydroformylation
  258586. Organoruthenium Catalyst
  258587. Ruthenium Complex
  258588. GK.5% over- reduction products were also isolatedM
  258589. 22294N
  258590. 2/28/96
  258591. ASRhodium-Catalyzed Hydroformylation of Internal Alkynes to a,b-Unsaturated Aldehydes
  258592. 1995X
  258593. 1760Y
  258594. GABRIEL WEATHERHEADw
  258595. alkyne -> alkene
  258596. Alkyne -> enal
  258597. De Clercq, P. J. B
  258598. Angew. Chem. Int. Ed. Engl. CBNickel Chloride
  258599. Chromium Chloride
  258600. Kishi Takai Nozaki Rxn
  258601. Enediyne
  258602. A826% C22 a-OTBS + 21% C22 b-OTBS + 6% C22 b-OTBS,C26 b-OH
  258603. 22295N
  258604. 2/28/96V@Estramycins:  A New Diyl Precursor Family Derived from EstradiolW
  258605. 1995X
  258606. 1749Y
  258607. GABRIEL WEATHERHEADw
  258608. aldehyde -> alcohol
  258609. Tietze, L. F.B
  258610. Angew. Chem. Int. Ed. Engl. C_Allylsilane
  258611. Conjugate Addition
  258612. Tin tetrachloride
  258613. Chiral Auxiliary
  258614. Chelation Control
  258615. Annulation
  258616. 22296N
  258617. 2/28/96
  258618. Intramolecular Allylsilane Addition to Chiral Alkylidene-1,3-dicarbonyl Compounds for the Synthesis of Enantiomerically Pure trans-1,2-Disubstituted Cyclopentanes and Cyclohexanes
  258619. 1995X
  258620. 1731Y
  258621. GABRIEL WEATHERHEAD
  258622. Overman, L. E.B
  258623. JACSC0Mannich Cyclization
  258624. Paraformaldehyde
  258625. Annulation
  258626. 22297N
  258627. 2/28/96V;Mannich Biscyclizations.  Total Synthesis of (-)-AjmalicineW
  258628. 1995X
  258629. 9139Y
  258630. GABRIEL WEATHERHEAD
  258631. A    Prein, M.B
  258632. JACSC
  258633. Diels-Alder Cycloaddition
  258634. 22298N
  258635. 2/28/96V
  258636. Highly Like-Selective [4+2] Cycloadditions of Chiral Dienols:  The Importance of 1,3-Allylic Strain in the Hydroxy-Directed StereocontrolW
  258637. 1995X
  258638. 9190Y
  258639. GABRIEL WEATHERHEAD
  258640. Hart, D. J.B
  258641. JACSCgIntramolecular Diels-Alder
  258642. Lewis Acid Catalyst
  258643. Diethylaluminum Chloride
  258644. Silical Gel
  258645. [4+2] CycloadditionI
  258646. endo/exo selectivity  = 20/1M
  258647. 22299N
  258648. 2/28/96V3Total Synthesis of (+)-Himbacine and (+)-HimbellineW
  258649. 1995X
  258650. 9369Y
  258651. GABRIEL WEATHERHEAD
  258652. Hart, D. J.B
  258653. CnLithium Carbanion
  258654. Sulfone Anion
  258655. Julia-Lythgoe Coupling
  258656. Olefin Synthesis
  258657. Beak Metalation
  258658. Schreiber Ozonolysis
  258659. 22300N
  258660. 2/28/96V3Total Synthesis of (+)-Himbacine and (+)-HimbellineW
  258661. 1995X
  258662. 9369Y
  258663. GABRIEL WEATHERHEADw
  258664. aldehyde -> alkene
  258665. Burk, M. J.B
  258666. JACSC3Chiral P Ligand 
  258667. DuPHOS
  258668. Organorhodium Complex
  258669. 22301N
  258670. 2/28/96
  258671. AkAsymmetric Catalytic Synthesis of b-Branched Aminoacids via Highly Enantioselective Hydrogenation Reactions
  258672. 1995X
  258673. 9375Y
  258674. GABRIEL WEATHERHEADw
  258675. alkene -> alkane
  258676. Keck, G. E. B
  258677. JOCC'Chiral Organotitanium Titanium CatalystI
  258678. 22302N
  258679. 2/28/96V
  258680. Catalytic Enantioselective Synthesis of Dihydropyrones via Formal Hetero Diels-Alder Reactions of Danishefsky
  258681. s Diene with AldehydesW
  258682. 1995X
  258683. 5998Y
  258684. GABRIEL WEATHERHEAD
  258685. Carretero, J. C.B
  258686. JOCC@Dieckmann Condensation
  258687. Lithium Carbanion
  258688. LHMDS
  258689. Michael Addition
  258690. 22303N
  258691. 2/28/96
  258692. AwEfficient Stereoselective Access to Polyhydroxylated Indolizidine Compounds Based on g-Hydroxy-a,b-unsaturated Sulfones
  258693. 1995X
  258694. 6000Y
  258695. GABRIEL WEATHERHEADw
  258696. ester -> ketone
  258697. Trost, B. M.B
  258698. JACSCHOrganoruthenium Ruthenium Complex
  258699. Indium trichloride
  258700. Aldehyde Synthesis
  258701. 22304N
  258702. 2/28/96V[Two-Metal Catalyst System for Redox Isomerization of Propargyl Alcohols to Enals and EnonesW
  258703. 1995X
  258704. 9586Y
  258705. GABRIEL WEATHERHEADw
  258706. propargyl alcohol -> enal
  258707. Evans, D. A.B
  258708. JACSCHAldol Reaction
  258709. Silyl Enol Ether
  258710. Boron Trifluoride
  258711. Open Transition State
  258712. 22305N
  258713. 2/28/96VODouble Stereodifferentiating Acid-Promoted (Mukaiyama) Aldol Bond ConstructionsW
  258714. 1995X
  258715. 9598Y
  258716. GABRIEL WEATHERHEADw
  258717. aldehyde -> alcohol
  258718. Sawamura, M.
  258719. Ito, Y.B
  258720. CPasymmetric hydrogenation
  258721. chiral Rh complex
  258722. amino acid synthesis
  258723. organorhodium 
  258724. 22306N
  258725. 2/28/96
  258726. Enantioselective Hydrogenation of b-Substituted a-Acetamidoacrylates Catalyzed by Rhodium Complexes with Trans-Chelating Chiral Phosphine Ligands
  258727. 1995X
  258728. 9602Y
  258729. GABRIEL WEATHERHEAD
  258730. A    Rossi, T.B
  258731. JACSC_b-Lactam
  258732. Allyl Borane
  258733. Organoboron Reagent
  258734. Lewis Acid
  258735. Diethylzinc
  258736. Triethylaluminum
  258737. HydroborationI
  258738. d.r. = 95/5M
  258739. 22307N
  258740. 2/28/96VpNovel Amidoalkylation of 4-Acetoxyazeidinones with Allylic Boranes.  A Stereoselective Entry into the TribactamsW
  258741. 1995X
  258742. 9604Y
  258743. GABRIEL WEATHERHEAD
  258744. Ito, Y.B
  258745. JACSC
  258746. Palladium Acetate
  258747. Organopalladium
  258748. Silylation
  258749. Oxidation
  258750. Silyl Baeyer-Villiger
  258751. Diol Synthesis
  258752. Asymmetric boration
  258753. Pentadienylborane
  258754. Organoborane
  258755. 22308N
  258756. 2/28/96
  258757. Diastereoselective Intramolecular Bis-Silylation of a Carbon-Carbon Double Bond.  A Highly Stereocontrolled Synthesis of (-)-AvenacolideW
  258758. 1995X
  258759. 9608Y
  258760. GABRIEL WEATHERHEAD
  258761. Snapper, M. L.B
  258762. JACSC2Organoruthenium
  258763. Ruthenium Reagent
  258764. Diene Synthesis
  258765. 22309N
  258766. 2/28/96VUSelective Ring-Opening Cross Metathesis.  Short Synthesis of Multifidene and ViridineW
  258767. 1995X
  258768. 9610Y
  258769. GABRIEL WEATHERHEAD
  258770. Corey, E. J.B
  258771. JACSCROrganoaluminum Catalyst
  258772. Aluminum Complex
  258773. [4+2] Cycloaddition
  258774. Cyclohexene SynthesisI
  258775. 22310N
  258776. 2/28/96VhEnantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder MethodologyW
  258777. 1995X
  258778. 9616Y
  258779. GABRIEL WEATHERHEAD
  258780. Corey, E. J.B
  258781. JACSCAAldol Condensation
  258782. Zinc Chloride
  258783. Lithium Enolate
  258784. Diene Synthesis
  258785. 22311N
  258786. 2/28/96VhEnantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder MethodologyW
  258787. 1995X
  258788. 9616Y
  258789. GABRIEL WEATHERHEAD
  258790. aldehyde -> alcohol
  258791. Sammakia, T.B
  258792. JOCCFDirected metalation
  258793. Butyl Lithium
  258794. TMEDA
  258795. Ferrocene Oxazoline
  258796. Carbanion
  258797. YKhOptimization of Ligand/base and solvent to provide substituted chiral ferrocenes via directed metalationM
  258798. 22312N
  258799. 2/28/96VZLigand Effects on the Stereochemistry of the Metalation of Chiral Ferrocenyloxazolines 
  258800. 1995X
  258801. 6002Y
  258802. GABRIEL WEATHERHEAD
  258803. Chiara, J. L.B
  258804. JOCCNAnnulation
  258805. Samarium Diiodide
  258806. Reductive Cyclization
  258807. Radical Anion
  258808. amino alcoholI
  258809. With six equivalents of SmI2 reductive cyclization occurs followed by cleavage of the N-O bond (if 25 equiv. of water is added) to provide the primary amine. M
  258810. 22313N
  258811. 2/28/96V
  258812. Intramolecular Reductive Coupling of Carbonyl-Tethered Oxime Ethers Promoted by Samarium Iodide:  A Powerful Method for the Stereoselective Synthesis of AminocyclopentitolsW
  258813. 1995X
  258814. 6010Y
  258815. GABRIEL WEATHERHEADw"aldehyde -> alcohol
  258816. oxime -> amine
  258817. Bertrand, M. P.B
  258818. CGChromium Acetate
  258819. Radical Cyclization
  258820. Annulation
  258821. Carbohydrate  ChemistryI
  258822. 22314N
  258823. 2/28/96V
  258824. 1,2- and 1,5-Stereocontrols in 5-Hexenyl Radical Cyclizations:  Cooperative or Antagonistic Effect.  Confrontation of Experimental Results with MM2 Calculations of Transition StatesW
  258825. 1995X
  258826. 6040Y
  258827. GABRIEL WEATHERHEAD
  258828. Kibayashi, C.B
  258829. JOCC5Silyl enol ether
  258830. Lewis Acid
  258831. hydrazonium ion addition
  258832. 22315N
  258833. 2/28/96V
  258834. Asymmetric Total Synthesis of (R)-Cryptopleurine and (R)-(-)-Julandine via Highly Enantioselective Amidoalkylations with N-Acylhydrazonium SaltsW
  258835. 1995X
  258836. 6114Y
  258837. GABRIEL WEATHERHEAD
  258838. Kibayashi, C.B
  258839. JOCC`Radical Cyclization
  258840. Photochemical Rxn
  258841. Annulation
  258842. tributyltin hydride
  258843. Intramolecular cyclization
  258844. 22316N
  258845. 2/28/96V
  258846. Asymmetric Total Synthesis of (R)-Cryptopleurine and (R)-(-)-Julandine via Highly Enantioselective Amidoalkylations with N-Acylhydrazonium SaltsW
  258847. 1995X
  258848. 6114Y
  258849. GABRIEL WEATHERHEAD
  258850. A    Fu, G. C.B
  258851. C.Tributyltin cyanide
  258852. Manders reagent
  258853. Acylation
  258854. 22317N
  258855. 2/28/96VqConvenient and Efficient Conversion of Aldehydes to Acylated Cyanohydrins Using Tributyltin Cyanide as a CatalystW
  258856. 1995X
  258857. 6229Y
  258858. GABRIEL WEATHERHEAD
  258859. Bachi, M. D.B
  258860. JOCCIRADICAL CYCLIZATION
  258861. TRIBUTYLTIN HYDRIDE
  258862. ISONITRILE
  258863. THIOLACTAM 
  258864. ANNULATIONI
  258865. 22318N
  258866. 2/28/96V
  258867. Stereocontrolled 5-Exo-Trig Cyclization of Imidoyl Radicals in the Synthesis of Substituted (Alkylthio)pyrrolines, Pyroglutamates, and ThiopyroglutamatesW
  258868. 1995X
  258869. 6242Y
  258870. GABRIEL WEATHERHEAD
  258871. Pancrazi, A.B
  258872. Tet. Lett.C.tributyltin hydride
  258873. Organostannane
  258874. Annulation
  258875. 22319N
  258876. 2/28/96VX6-Endo-Trig Radical Cyclizations:  Synthetic Approaches to the A-B Ring of (
  258877. )-ForskolinW
  258878. 1995X
  258879. 7247Y
  258880. GABRIEL WEATHERHEAD
  258881. Schmalz, H-G.B
  258882. Angew. Chem. Int. Ed. Engl. CFAlkylidine Complexes Annulation
  258883.  Ruthenium Carbene
  258884. Molybdenum Carbene
  258885. ReviewM
  258886. 22320N
  258887. 2/28/96
  258888. VnCatalytic Ring Closing Metathesis:  A New,  Powerful Technique for Carbon-Carbon Coupling in Organic SynthesisW
  258889. 1995X
  258890. 1833Y
  258891. GABRIEL WEATHERHEADw
  258892. diene -> alkene
  258893. Lautens, M. B
  258894. Can. J. Chem.C
  258895. Samarium  
  258896. Cyclopropane
  258897. Palladium or Nickel 
  258898. Transition Metal Catalyst
  258899. [3+2] Cycloaddition Methylenecyclopropane
  258900. Oxabicyclic Ring Opening
  258901. HydroaluminationK
  258902. ReviewM
  258903. 22321N
  258904. 2/28/96V|New Strategies for the Stereoselective Synthesis of Natural and Unnatural Products via Organometallic Reagents and CatalystsW
  258905. 1995X
  258906. 1251Y
  258907. GABRIEL WEATHERHEAD
  258908. Baba, A.B
  258909. Chem. Lett.C>Organostannane
  258910. Trimethylsilyl chloride
  258911. Allylation
  258912. Tin Reagent
  258913. 22322N
  258914. 2/28/96VhChlorotrimethylsilane Acetonitrile System as a New Promoter for Carbonyl Allylation by DiallyldibutyltinW
  258915. 1995X
  258916. GABRIEL WEATHERHEADw(aldehyde -> homoallylic alcohol or ether
  258917. Mukaiyama, T. B
  258918. Chem. Lett.C@Lewis Acid
  258919. Magnesium Bromide
  258920. Silyl Ketene Acetal
  258921. Aldol Reaction
  258922. The above aldehyde was prepared via an asymmetric aldol construction mediated by Sn(OTf)2, dibutyl tin acetate and a chiral diamineM
  258923. 22323N
  258924. 2/28/96V
  258925. A Novel Approach to the Synthesis of Taxol.  A Synthesis of Optically Active 3,7-dibenzyloxy-4,8-di-t-butyl-dimethylsiloxy-5,5-dimethyl-6-methoxybenzyloxy-2-octanone by way of Stereoselective Aldol ReactionsW
  258926. 1995X
  258927. GABRIEL WEATHERHEADw
  258928. aldehyde -> alcohol
  258929. Mukaiyama, T. B
  258930. Chem. Lett.CHIntramolecular  SmI2 Reformatsky Cyclization
  258931. Samarium Iodide
  258932. Annulation
  258933. 22324N
  258934. 2/28/96VFAn Asymmetric Synthesis of Fully Functionalized B Ring System of TaxolW
  258935. 1995X
  258936. GABRIEL WEATHERHEAD
  258937. Mukaiyama, T. B
  258938. Chem. Lett.CDAnnulation
  258939. Aldol Cyclization
  258940. Cerium Trichloride
  258941. Cerium Enolate
  258942. 22325N
  258943. 2/28/96V{Synthesis of AB Ring Model System of Taxol via Allylation of 8-Membered Ring Compound and Intramolecular Aldol CondensationW
  258944. 1995X
  258945. GABRIEL WEATHERHEAD
  258946. Hashimoto, Y. 
  258947. Saigo, K.B
  258948. Chem. Lett.CBOrganolithium 
  258949. Propargyl Lithium
  258950. Diastereoselective 
  258951. Chiral Amine
  258952. 22326N
  258953. 2/28/96
  258954. A}Stereoselective Addition Reaction of Organolithium Reagents to Chiral Imines Derived from erythro-2-Amino-1,2-diphenylethanol
  258955. 1995X
  258956. GABRIEL WEATHERHEADw
  258957. imine -> amine
  258958. Kocienski, P.B    SynthesisCPCuprate
  258959. Organocopper
  258960. Organostannane
  258961. Transmetalation
  258962. Vinyl lithium
  258963. Organolithium
  258964. 22327N
  258965. 2/28/96VHA Synthesis of (3R*, 4R*)-Luffariolide E via 1,2-Metallate RearrangementW
  258966. 1995X
  258967. 1007a
  258968. GABRIEL WEATHERHEAD
  258969. Gennari, C.B
  258970. JOCC<Aldol Condensation
  258971. Chiral Boron Enolate
  258972. Felkin-Anh Addition
  258973. lAchiral enolates tend to preferentially afford anti aldol products derived from a Felkin-Anh  approach to the aminoaldehyde (Re face approach). 
  258974. The chiral boron enolate described above (LX = ent-4) provides the anti-Felkin product (3,4-syn-mismatched case) while in the matched case (LX = 4) the 3,4-anti aldol adduct is produced with high a diastereomeric ratio.
  258975. 22328N
  258976. 2/28/96
  258977. Reagent Control in the Aldol Addition  Reaction of Chiral Boron Enolates with Chiral a-Amino Aldehydes.  Total Synthesis of (3S,4S)-Statine
  258978. 1995X
  258979. 6248Y
  258980. GABRIEL WEATHERHEADw
  258981. aldehyde -> alcohol
  258982. A    Ko, S. Y.B
  258983. JOCC4nucleophilic ring opening
  258984. Asymmetric Dihyroxylation
  258985. 22329N
  258986. 2/28/96VEVicinol Diol Cyclic Thionocarbonates:  Like Cyclic Sulfates, and MoreW
  258987. 1995X
  258988. 6250Y
  258989. GABRIEL WEATHERHEAD
  258990. Shoji Kajigaeshi
  258991. et al.B
  258992. Chem Soc Japan CL
  258993. CNIodination
  258994. phenol
  258995. chloroiodine
  258996. halogenation
  258997. ester
  258998. phenolic
  258999. iodophenolI
  259000. iKAReaction done at r.t.
  259001. 2.1 eq of BTMA ICl2
  259002. Yields >70%   Most >90%M
  259003. 22330N
  259004. 2/28/96VFIodination of Phenols by Use if Benzyltrimethylammonium DichloroiodateW
  259005. 1987X
  259006. 2109\
  259007. Halogenation - Phenola
  259008. GABRIEL WEATHERHEAD
  259009. Rai-Shung LiuB
  259010. JACSC
  259011. cyclocarbonylation
  259012. metal
  259013. lactone
  259014. stereocontrol
  259015. propargyl halide
  259016. alkyne
  259017. stereoselective
  259018. stoichiometric
  259019. tungsten
  259020. triflic acid
  259021. demetalationI
  259022. W = CpW(CO)2
  259023. Yields 87 - 91%M
  259024. 22331N
  259025. 2/28/96V}Stereochemical Course in Tungsten-Promoted Cyclocarbonylation Reactions To Form Five-, Six-, and Seven-Membered Lactone RingsW
  259026. 1995X
  259027. 2933Y
  259028. v117\
  259029. lactonesa
  259030. GABRIEL WEATHERHEAD
  259031. A#William E. Crowe
  259032. Michael J. RachitaB
  259033. JACSCWreductive
  259034. catalytic
  259035. silane
  259036. siloxane
  259037. silyl
  259038. protected
  259039. cyclization
  259040. alkyne
  259041. alkene
  259042. propargylI
  259043. 22332N
  259044. 2/28/96VMTitanium-Catalyzed Reductive Cyclization of Unsaturated Ketones and AldehydesW
  259045. 1995X
  259046. 6787Y
  259047. v117\
  259048. Cyclization - Transition Metal
  259049. GABRIEL WEATHERHEADy
  259050. Emory Univ.
  259051. H.C. BrownB
  259052. JOCCtBMS
  259053. reduction
  259054. reduce
  259055. review
  259056. borane dimethyl sulfide
  259057. ester
  259058. nitrile
  259059. amide
  259060. BF3 Et20
  259061. boron triflouride etherate
  259062. carbonylK,Review paper with emphasis on removal of DMSM
  259063. 22333N
  259064. 2/28/96V
  259065. Selective Reductions. 29. A Simple Technique To Achieve an Enhanced Rate of Reduction of Representitive Organic Compounds by Borane-Dimethyl SulfideW
  259066. 1982X
  259067. 3153Y
  259068. 47 :16\
  259069. Reduction - BMSa
  259070. GABRIEL WEATHERHEADw0amide -> amine
  259071. ester -> alcohol
  259072. nitrile -> amine
  259073. Peter BeakB
  259074. Tet. Lett.CTN-alkyl
  259075. methoxyamine
  259076. secondary amine
  259077. indolene
  259078. aromatic organolithium
  259079. intramolecular
  259080. Yields 23-63%M
  259081. 22334N
  259082. 2/28/96ViThe Electrophilic Amination of Organolithiums With Methyllithium Complexes of N-Substituted MethoxyaminesW
  259083. 1983X
  259084. 24 : 6\
  259085. Heterocycle(N) - Indolenea
  259086. GABRIEL WEATHERHEADy
  259087. U. Illinois|
  259088. CH3NH+
  259089. A!Michael W. Rathke
  259090. Alan A. MillardB
  259091. CNnickel (II) bromide
  259092. retention
  259093. stereochemical
  259094. bromostyrene
  259095. vinyl halide
  259096. alkene
  259097. complete retention of configuration. Evidense against radical mechanism. Addition of phosphine reagent inactivates reaction
  259098. Reaction done with aryl halides (Br, I, Cl) as well as various vinyl halidesM
  259099. 22335N
  259100. 2/28/96VLA Nickel Catalyst for the Arylation and Vinylation of Lithium Ester EnolatesW
  259101. 1977X
  259102. 4833Y
  259103. 99 : 14\
  259104. Nickel - Couplinga
  259105. GABRIEL WEATHERHEADy
  259106. Michigan State
  259107. Eric J. RoskampB
  259108. Tet. Lett.CIester
  259109. amide
  259110. secondary
  259111. intramolecular
  259112. nucleophilic
  259113. amine
  259114. Sn[N(TMS)2]2
  259115. 1-Phenylethylamine   97%
  259116. 4-Methoxyaniline   92%
  259117. Benzylamine    93%
  259118. 2-Methoxyethylamine    98%
  259119. t-Butylamine    87%
  259120. also describes method of using glycol ester w/o ethanolamineM
  259121. 22336N
  259122. 2/28/96VFDirect Conversion of Esters to Secondary Amides using Tin(II) ReagentsW
  259123. 1993X
  259124. 7217Y
  259125. v.34 No.45\
  259126. amides - from estersa
  259127. GABRIEL WEATHERHEADw
  259128. ester -> amidey
  259129. Northwestern|
  259130. A!David A. Shirley
  259131. Philip A RousselB
  259132. JACSC\metalation
  259133. indole
  259134. lithiation
  259135. N-Methyl
  259136. N-Phenyl
  259137. N-subtituted
  259138. n-Butyllithium
  259139. 2-carboxylic acidI
  259140. oKDQuench with ketone, aldehyde isocyanate, methyl sulfonate, quinolineM
  259141. 22337N
  259142. 2/28/96VKMetalation of Indole, N-Methylindole and N-Phenylindole with n-ButyllithiumW
  259143. 1953X
  259144. Lithiation - Indolea
  259145. GABRIEL WEATHERHEAD
  259146. Jean Piere GenetB
  259147. Tet. Lett.Ciprotecting group
  259148. deprotection
  259149. deprotect
  259150. allylamine
  259151. amine
  259152. palladium
  259153. mercaptobenzoic acid
  259154. diallyl
  259155. selectiveI
  259156. pK=Reacted at 60C for 30 min
  259157. 100% yield
  259158. now effect on chiralityM
  259159. 22338N
  259160. 2/28/96V6Selective Deprotection of Allyl Amines using PalladiumW
  259161. 1995X
  259162. 1267Y
  259163. 36:8\
  259164. Protecting Groups - Allyla
  259165. GABRIEL WEATHERHEADw
  259166. N-Allyl -> NH
  259167. Hiroki YamanakaB
  259168. Tet. Lett.Cghetero
  259169. nucleophile
  259170. Fluorovinamidinium
  259171. guanidine
  259172. pyrimidine
  259173. fluoro
  259174. fluorinated
  259175. one-pot
  259176. vinamidinium saltI
  259177. qK:Solvent = MeCN
  259178. Base = Et2NH, MeONa
  259179. R= Ph, Me, H, NH2, NHMeM
  259180. 22339N
  259181. 2/28/96
  259182. Reactions of B-Fluorovinamidinium Salt with Bifunctional Hetero Nucleophiles. A New Synthetic Route to Fluorinated HeterocyclesW
  259183. 1995X
  259184. 1527Y
  259185. 36:9\
  259186. Heterocycle(N) - pyrimidinea
  259187. GABRIEL WEATHERHEAD
  259188. Hans Schick
  259189. B    Angew IntC
  259190. glycidic ester
  259191. lactone
  259192. darzen
  259193. LiICA
  259194. one-pot
  259195. chlorocarboxylate
  259196. lithiation
  259197. lithium
  259198. phenolate
  259199. phenoxide
  259200. lithium N-cyclohexyl-N-isopropylamideI
  259201. LiICA = lithium N-cyclohexyl-N-isopropylamide
  259202. Yields ~ 80%
  259203. R1 = Me, Et, t-Bu, EtPh
  259204. R2 = Me, Et, H
  259205. Also cyclopentanone and cyclopropanoneM
  259206. 22340N
  259207. 2/28/96
  259208. Unexpected Course of the Darzens Reaction of Phenyl Esters of a-Chlorocarboxylic Acids with Carbonyl Compounds -- A Novel One-Step Synthesis of a-Chloro-b-lactones
  259209. 1995X
  259210. 2028Y
  259211. 34:18\
  259212. lactones - B-lactonesa
  259213. GABRIEL WEATHERHEADw
  259214. ester -> lactone
  259215. Janet W. Grissom
  259216. B    Angew IntCEenediyne
  259217. enyne
  259218. allene
  259219. ketene
  259220. radical
  259221. cyclization
  259222. cyclize
  259223. indene
  259224. 5-exoI
  259225. 22341N
  259226. 2/28/96VyLow-Temperature Tandem Enyne Allene Radical Cyclizations: Efficient Synthesis of 2,3-Dihydroindenes from Simple EnediynesW
  259227. 1995X
  259228. 2037Y
  259229. 34:18\
  259230. cyclization - enediynea
  259231. GABRIEL WEATHERHEADy
  259232. U. Utah
  259233. Giuseppe BartoliB    Angew IntC
  259234. stereoselective
  259235. organolithium
  259236. nucleophilic addition
  259237. cerium chloride
  259238. b-ketophosphine oxide
  259239. diastereoselective
  259240. b-hydroxyphosphine oxide
  259241. trisubstituted alkenes
  259242. tK/Also done w/ BuLi and MeLi with similar resultsM
  259243. 22342N
  259244. 2/28/96VQCerium(III) Chloride Promoted Nucleophilic Addition Of Organolithium Reagents to W
  259245. 1995X
  259246. 2046Y
  259247. 34:18\
  259248. alkenes - trisubstituteda
  259249. GABRIEL WEATHERHEADw  b-ketophosphine oxide -> alkene
  259250. A5W. Russell Bowman
  259251. Peter T. Stephenson
  259252. Adrian R. YoungB
  259253. Tet. Lett.
  259254. radical cyclization
  259255. cyclize
  259256. heterocycle
  259257. intramolecular
  259258. imine
  259259. nitrogen
  259260. one-pot
  259261. tandem
  259262. Bu3SnH
  259263. pyrrolidine
  259264. bicycle
  259265. spirocycle
  259266. spirocyclic
  259267. 5 6 exo
  259268. spiroamine
  259269. lewis acid
  259270. MgBr2 Et2O
  259271. selenium
  259272. phenyl
  259273. organo
  259274. indolizidine
  259275. pyrrolizidine
  259276. when R1 and/or R2 = H or PhCH2CH2 then both A and B are formed.
  259277. If R1 and or R2 are Ph then B dominates due to radical stabilizationM
  259278. 22343N
  259279. 2/28/96VMSynthesis of Nitrogen Heterocycles using Tandem Radical Cyclisation of IminesW
  259280. 1995X
  259281. 5623Y
  259282. 36:31\
  259283. heterocycle(N) - pyrolea
  259284. GABRIEL WEATHERHEAD
  259285. Francois GuibeB
  259286. Tet. Lett.Cqprotecting group
  259287. allyl
  259288. palladium
  259289. deprotect
  259290. carbonate
  259291. carbamate
  259292. phenol
  259293. phenoxide
  259294. carboxylate
  259295. ester
  259296. scavenger
  259297. silylK_Removal with either PhSiH3 or CF3CON(SiMe3)CH3
  259298. used to remove allyl in presence of Boc and FmocM
  259299. 22344N
  259300. 2/28/96VxNew Allyl Group Acceptors for Palladium Catalyzed Removal of Allylic Protections and Transacylation of Allyl Carbamates.W
  259301. 1995X
  259302. 5741Y
  259303. 36:32\
  259304. protecting groups - allyla
  259305. GABRIEL WEATHERHEAD
  259306. J.R. FalckB
  259307. Tet. Lett.C
  259308. mitsunobu
  259309. alcohol
  259310. nitrile
  259311. cyclization
  259312. cyclize
  259313. desulfonylation
  259314. phenylsulfonyl acetonitrile
  259315. dehydrate
  259316. magnesium Mg
  259317. HgCl2
  259318. dehydrationI
  259319. diol gives cyclized materialM
  259320. 22345N
  259321. 2/28/96V8Two-Carbon Elongation/Annulation of Alcohols to NitrilesW
  259322. 1995X
  259323. 5691Y
  259324. 36:32\
  259325. Nitrile - from Alcohola
  259326. GABRIEL WEATHERHEAD
  259327. Marco A. CiufoliniB
  259328. Tet. Lett.Cv2,2,2,-trichloroethyl
  259329. carbamate
  259330. carbonate
  259331. ester
  259332. neutral
  259333. amine
  259334. alcohol
  259335. deprotection
  259336. cadmium lead
  259337. removalK9used successfully with sec amines, anilines, and indoles.M
  259338. 22346N
  259339. 2/28/96VSReductive Cleavage of TROC Groups Under Neutral Conditions with Cadmium-Lead CoupleW
  259340. 1995X
  259341. 5681Y
  259342. 36:32\
  259343. Protecting Groups - TROCa
  259344. GABRIEL WEATHERHEADy
  259345. Rice Univ.
  259346. Keith R. BuszekB
  259347. Tet. Lett.Clarylation
  259348. propargylic
  259349. alcohol
  259350. coupling
  259351. couple
  259352. cross
  259353. palladium
  259354. migration
  259355. phosphine
  259356. copper
  259357. cuprate
  259358. Pd(0)-Cu(I)I
  259359. base = piperidine or diisopropylamine
  259360. R2 = Ph
  259361. R3 = OTBS when base is diisopropylamine and Ph when base is piperidine
  259362. R4 = H or TBS
  259363. also toluyl and furyl phosphines were used with yields of 95%
  259364. R1 = Me, Et, PhM
  259365. 22347N
  259366. 2/28/96VrUnexpected Arylation of Tertiary Propargylic Alcohols During Attempted Palladium Catalyzed Cross-Coupling ReactionW
  259367. 1995X
  259368. 5677Y
  259369. 36:32\
  259370. Palladium - Alkynea
  259371. GABRIEL WEATHERHEADy
  259372. Kansas State Univ.
  259373. Padwa, A. B
  259374. J. Org. Chem.CHannulation
  259375. diazo imide
  259376. rhodium acetate
  259377. indole
  259378. Lawesson reagent
  259379. vindolineI
  259380. 1315N
  259381. 10/22/95VlTandem Cyclization Cycloaddition Reaction of Rhodium Carbeniods as an Approach to the Aspidosperma AlkaloidsW
  259382. 1995X
  259383. 6258Y
  259384. GABRIEL WEATHERHEAD
  259385. 21340
  259386. J.W.Dankwardt
  259387. Srebnik, M.B
  259388. J. Org. Chem.CJorganozircoium
  259389. Lewis acid 
  259390. zinc chloride
  259391. copper chloride
  259392. zirconium reagentI
  259393. WEATHERHEAD
  259394. 21341
  259395. unreg
  259396. Yesf)x
  259397.     Helvetica
  259398. Geneva
  259399. Symbol
  259400. Chicago
  259401. New York
  259402. Bauhaus 93
  259403. Stencil
  259404. Athens
  259405. Bookman Old Style Bold
  259406. Century Gothic
  259407. Times
  259408.     Desdemona
  259409.     Espi Sans
  259410. Matura MT Script Capitals
  259411. Mistral
  259412. Vivaldi
  259413. Brush Script MT
  259414. Braggadocio
  259415. Arial
  259416. Arial Rounded MT Bold
  259417. Playbill
  259418. MT Extra
  259419. Copy Structure
  259420. nulltell application "CS ChemDraw Pro
  259421. activate
  259422. repeat until (count  documents) = 0
  259423. close front document  saving no
  259424. end repeat
  259425. make new document
  259426. do menu item "Paste"
  259427. end tell
  259428. FasdUAS 1.101.10
  259429. .miscactvnull
  259430. .coreclosnull
  259431. paste to struc
  259432. Print A Card
  259433. Author Index
  259434. Keyword Index
  259435. Reference Index
  259436. copy1
  259437. Find Transformation
  259438. Transormation Index
  259439. savono  
  259440. .corecnte****
  259441. .corecrel****
  259442. .miscmenunull
  259443. Paste
  259444. CS ChemDraw Pro
  259445. Macintosh HD
  259446. CS ChemDraw Pro
  259447. APPLCHMD
  259448. CS ChemDraw Pro
  259449. FMacintosh HD:Chemistry:ChemOffice Pro:CS ChemDraw Pro:CS ChemDraw Pro
  259450. mgabr6
  259451. Macintosh HD
  259452. Macintosh HD
  259453. .aevtoappnull
  259454. .aevtoappnull
  259455. .miscactvnull
  259456. .corecnte****
  259457. savono  
  259458. .coreclosnull
  259459. .corecrel****
  259460. .miscmenunull
  259461. Macintosh HD
  259462. CS ChemDraw Pro
  259463. APPLCHMD
  259464. CS ChemDraw Pro
  259465. FMacintosh HD:Chemistry:ChemOffice Pro:CS ChemDraw Pro:CS ChemDraw Pro
  259466. .aevtoappnull
  259467. .aevtoappnull
  259468. nulltell app "CS ChemDraw Pro
  259469.      do menu item "Select All"
  259470.      do menu item "Copy"
  259471. end tellFasdUAS 1.101.10
  259472. .miscmenunull
  259473. Select All
  259474. .miscmenunull
  259475. CS ChemDraw Pro
  259476. Macintosh HD
  259477. CS ChemDraw Pro
  259478. APPLCHMD
  259479. CS ChemDraw Pro
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  259481. mgabr6
  259482. Macintosh HD
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  259492. CS ChemDraw Pro
  259493. APPLCHMD
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  259496. mgabr6
  259497. Macintosh HD
  259498. Macintosh HD
  259499. Find Synthon
  259500. print marked
  259501. copper
  259502. copper
  259503. copper
  259504. copper
  259505. Unmark
  259506. Unmark All
  259507. Find Marked
  259508. card number
  259509. <A    Find Date
  259510. Find and Unmark
  259511. Open Script
  259512. thiel2
  259513. thiel3
  259514. thiel4
  259515. master search
  259516. S = "AND"
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  259527. Cancel
  259528. Cancel
  259529. KeySearchprimer
  259530.  )  <  0
  259531. copper   coupl
  259532.    couplV
  259533. copper
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  259535. copper
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  259537. copper
  259538. copper|
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  259541.    coupl
  259542. copperV
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  259544. copper   coupl
  259545. copperC
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  259547. copperK
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  259549. copper|
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  259551. copperw
  259552.    coupl
  259553. copperV
  259554.    coupl
  259555.    couplC
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  259557. copper   coupl
  259558. copperK
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  259560. copper|
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  259562. copperw
  259563.    coupl
  259564. copperV
  259565.    coupl
  259566.    couplK
  259567. copper
  259568.    couplK
  259569. copper
  259570. copper   coupl
  259571. copper|
  259572.    coupl
  259573. copperw
  259574.    coupl
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  259599. X ="Yes"
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  259603. f = "and"
  259604. h = "and"
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  259606. KeySearchSecondaryNot
  259607. Cancel
  259608. HnYou Must Have A Search Criteria In The First Search BoxC'
  259609. \ = "and"
  259610. X ="Yes"
  259611. ^ ="and"
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  259613. ` ="and"
  259614. f = "and"
  259615. h = "and"
  259616. \ = "none"
  259617. SubSearchAnd
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  259619. X = "Yes"
  259620. ^ = "and"
  259621. _ = "and"
  259622. ` = "and"
  259623. f = "and"
  259624. h = "and"
  259625. thiel1
  259626. startup
  259627. tin        paquette
  259628.         paquetteV
  259629.         paquetteV
  259630.         paquette
  259631.         paquette
  259632. tin        paquette
  259633.         paquette
  259634.         paquette
  259635.         paquette
  259636.         paquetteC
  259637.         paquette
  259638.         paquette
  259639.         paquette
  259640.         paquetteK
  259641. tin        paquette
  259642.         paquette
  259643. X = "Yes" 
  259644. W = "Yes"
  259645.   & " " & 
  259646. X = "Yes"  
  259647. W = "No"
  259648. X = "No"  
  259649. W = "Yes"
  259650. ^ = "and"  
  259651. T = "and"
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  259654. T = "and"
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  259657. _ = "and"  
  259658. U = "and"
  259659.   &   " " & 
  259660. _ = "and"  
  259661. U = "not"
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  259663. U = "and"
  259664. ` = "and"  
  259665. V = "and"
  259666.   &   " " & 
  259667. ` = "and"  
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  259671. f = "and"  
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  259684. k = "and"
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  259698.  "12in"
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  259702. m = "15in" 
  259703. m = "12in" 
  259704. m = "17in" 
  259705. m = "15in" 
  259706. set all on
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  259717. find and switch
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  259720. V@S@?
  259721. BgThank You for your help in making SynRef a better programC
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  259723. That's not quite it. Try it again.
  259724. cancel find
  259725. register
  259726. Will Do!
  259727. Cancel
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  259844. .WWW!OURLlong
  259845. x = "CAS"
  259846. nulltell application "Netscape"
  259847. OpenURL 
  259848.  "info.cas.org/welcome.html"
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  259851. info.cas.org/welcome.html
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  259864. .WWW!OURLlong
  259865. x = "NIH"
  259866. Tnulltell application "Netscape"
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  259871. 8http://molbio.info.nih.gov:80/modeling/quick_finder.html
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  259918. Index Journals
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  259923. passoff
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  259940. Monaco
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  260116. |vnwk]ghQjldVat
  260117. {tof]
  260118. hGms3{~i7B]x~
  260119. yqiaZ^TSS[fu
  260120. vj^QE=H321EO`fx
  260121. zsnie`elz
  260122. yoi]UNJBFO]n|
  260123. |yjb_ls
  260124. |xwuux{
  260125. {xu*srtuy~
  260126. xtqqsvz
  260127. z|wnp|
  260128. umjmptx~
  260129. mSTSbpotwz}
  260130. a;;4Re\`behmhi}
  260131. qd[TRNP[bkrx|
  260132. VG;50-.?FRZaehijnssgemoz
  260133. uj`WRWYbmu{
  260134. {urqx
  260135. |l[NA617:FR]chloprnib\^^fr
  260136. ~uojox
  260137. soPFC
  260138. `[ugmquyyvpf[WRXet
  260139. tvYJad
  260140. skWuOrzi
  260141. xg^X[dp
  260142. znhfmv
  260143.  L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/F
  260144. sc/scale
  260145. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/G
  260146. fI R/fS R/fZ R/fl
  260147. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDH
  260148. st R/bDst R/sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  260149. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m 
  260150. a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  260151. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e J
  260152. P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  260153. x}b/sRmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpK
  260154. A{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  260155. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  260156. 0 cw 2 dv xl
  260157. aR aL m n D aL a 0 p M 0L
  260158.  o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  260159. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  260160. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  260161. St 16 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  260162.  32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  260163. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  260164. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  260165. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/N
  260166. Ha{gs np 3 1 r
  260167. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  260168. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL O
  260169. 0 aR aL m 180 aA s 180 aA a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  260170. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/P
  260171. CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  260172. P P}{sq at 2
  260173. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  260174. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b
  260175. /RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  260176. l w .35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  260177. w n p l w 2 m DR
  260178.  n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  260179. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -S
  260180. 1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  260181. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CT
  260182. A OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  260183. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  260184. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{
  260185. 0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  260186. 21 -10 27 -8 27 0 cv
  260187. 27 8 21 10 9 6 cv
  260188. -3 2 -3 -2 9 -6 cv
  260189. cp}b/DLB{0 0 M -4.8 4.8V
  260190. -8 8 -9.6 12 -9.6 16.8 cv
  260191. -9.6 21.6 -8 24.6 -4.8 25.8 cv
  260192. -1.6 27 1.6 27 4.8 25.8 cv
  260193. 8 24.6 9.6 21.6 9.6 16.8 cv
  260194. 9.6 12 8 8 4.8 4.8 cv
  260195. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whfW
  260196. {gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  260197. 0 Y X Y rO ac
  260198. X Y X 0 rO ac
  260199. X 0 0 0 rO ac
  260200. 0 0 0 Y rO ac
  260201. cp}b/Rc{0 0 p M
  260202. 0 Y p l
  260203. X Y p l
  260204. X 0 p l
  260205. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/grX
  260206. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  260207. m D 0 lt{n}if sq n D
  260208. CMT dtransform idtransform
  260209. e 2 m e
  260210. 7 m 32 a 256 dv D sc}b/gLB{sh{
  260211. 32 -0.5 0.5{gs
  260212. 13.5 0 xl
  260213. D 32 s 64 dv 13.5 m D 7 m 24 dv
  260214. -13.5 0 xl
  260215. gr}for
  260216. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  260217. 32 -0.5 0.5{gs
  260218. D 32 s 64 dv 0.65 m D
  260219. gr}for
  260220. Cr SM st}{Cr grf}ie}b/gAc{sh{sZ
  260221. 32 -0.5 0.5{gs
  260222. D 32 s 64 dv D
  260223. gr}for
  260224. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  260225. 32 -0.5 0.5{gs
  260226. 0 13.5 xl
  260227. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  260228. 0 -13.5 xl
  260229. DLB f
  260230. gr}for
  260231. DLB SM st}{DLB grf}ie}b/gRr{sh{sRm[
  260232. 32 -0.5 0.5{gs
  260233. X 2 dv Y 2 dv xl
  260234. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  260235. X -2 dv Y -2 dv xl
  260236. gr}for
  260237. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  260238. 32 -0.5 0.5{gs
  260239. X 2 dv Y 2 dv xl
  260240. D 32 s 64 dv X Y lt{X}{Y}ie m 0\
  260241. .25 m D
  260242. X -2 dv Y -2 dv xl
  260243. gr}for
  260244. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  260245. rev{1 -1 sc}if
  260246. 0 lW 2 m xl
  260247. D SA OA
  260248. ad 0 xl
  260249. 180 ro
  260250. 0 lW 2 m xl
  260251. SA OA}b/Aos{X Y M SM cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  260252. o 0 lt o 0 lt ne/rev x
  260253. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div^
  260254.  D 2 S lt{P 2 S}if/lp x
  260255. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  260256. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  260257. lp 0 p M
  260258. 0 0 0 Y lp ac
  260259. 0 Y 2 dv lp neg o lp ac
  260260. 0 Y 2 dv 0 Y lp ac
  260261. 0 Y l_
  260262. p Y lp ac
  260263. X lp s 0 p M
  260264. X 0 X Y lp ac
  260265. X Y 2 dv X lp a o lp ac
  260266. X Y 2 dv X Y lp ac
  260267. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA a arc st
  260268. np X Y s Y 2 dv
  260269. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p`
  260270. rO D rlineto
  260271. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  260272. rO lW -2 dv a Y lW 2 dv a rO a p l
  260273. lW -2 dv Y lW 2 dv a p l
  260274. 0 Y p l X Y p l X 0 p l cp f
  260275. 0 0 p M
  260276. 0 Y p l
  260277. X Y p l
  260278. X 0 p l cp
  260279. SM st}{Rr SM st}{rO Y p M rO rO 
  260280. 0 Y X Y rO ac
  260281. X Y X 0 rO ac
  260282. X 0 0 0 rO ac
  260283. rO neg D xl X Y 0 Y rO ac
  260284. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  260285. -1 -1 sc LB whf}{Asc gs gLB gr
  260286. -0.4 -0.4 sc LB whf}{b
  260287. Asc LB gs whf gr
  260288. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  260289. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  260290. gs 3.6 12 sc gOv gr
  260291. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  260292. gs 3.6 12 sc Cr whf gr
  260293. B}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  260294. 0 -1 p M
  260295. 0 0 1 0 1 ac
  260296. 8 0 8 1 1 ac
  260297. 8 0 16 0 1 ac
  260298. 16 0 16 -1 1 ac
  260299. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY Dd
  260300.  X Y dt 0 0 M SM cpt xl
  260301. 2 dv D sc
  260302. 1 0 M -1 0 l
  260303. 0 1 M 0 -1 l
  260304. Ast}{XY D X Y dt 0 0 M SM cpt xl
  260305. 2 dv D sc
  260306. 1 0 M -1 0 l
  260307. Ast}{4.5 Aos
  260308. 1 0 M -1 0 l
  260309. 0 1 M 0 -1 l
  260310. 2 0 M 0 0 2 0 360 arc
  260311. Ast}{4.5 Aos
  260312. 1 0 M -1 0 l
  260313. 2 0 M 0
  260314.  0 2 0 360 arc
  260315. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  260316. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  260317. 1 -1 M -1 -1 l
  260318. 0 2 M 0 -2 l
  260319. Ast}{5 Aos
  260320. 1 -1 M -1 -1 l
  260321. 1 1 M -1 1 l
  260322. 0 2 Mf
  260323.  0 -2 l
  260324. Ast}{4.5 Aos
  260325. 1 0 M -1 0 l
  260326. 0 1 M 0 -1 l
  260327. Ast}{4.5 Aos
  260328. 1 0 M -1 0 l
  260329. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs whf gr
  260330. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  260331. s 3.6 12 sc Cr whf gr
  260332. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  260333. gs 3.6 12 sc Cr blf gr
  260334. ZLB whf}{Asc LB gs whf gr
  260335. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  260336. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gh
  260337. s SM st gr
  260338. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  260339. e 2 ix a}b
  260340. /PT{D 2 4 gi al P OP D 1 sc
  260341. o length 6 gt{P 6 g}{e P 8 dv}ie
  260342. D lW 2 m lt{P lW 2 m}if
  260343. 0 e p
  260344. 0 0 p
  260345. 3 -1 r s 3 1 r e s e
  260346. 0 0 p M 1 0 p l
  260347. 0 0 p ap M 1 0 p ap l
  260348. e n e n
  260349. 0 0 p ap M 1 0 p ap l
  260350. P P}b
  260351. f/DT{gs np PTj
  260352.  SM st gr}b/NH{lW s D hS dv ru
  260353. cvi D 0 eq{P 1}if/nH x
  260354. D hS nH m s
  260355. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  260356. bW 2 dv/bd x
  260357. lW 2 dv e D NH e{k
  260358. D bd p M bd n p l}for
  260359. st gr}{gs 12 OB np
  260360. lW 2 dv 0 xl NH 1 sc
  260361. bW 2 dv wF m nH 1 a dv/bd x
  260362. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  260363. np 0 lW 2 dv o o n p M p l bW 2 dv
  260364. wF m o o p l n p l
  260365. cp fl
  260366.  gr}{P}{gs 12 OB/bL x
  260367. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  260368. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  260369. bL nSq 2 m dv D sc
  260370. nSq{.135  .667 .865  .667 1 0 rcurveto
  260371. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{
  260372. gs 12 OB
  260373. np 0 lW 2 dv o o n p M p l bW 2 dv
  260374. wF m o o p l n p l
  260375. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  260376. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}n
  260377. {DT}}o 0 g g xc}b
  260378. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  260379. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  260380. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  260381. 5 -1 r dv neg e 5 -1 r dv neg e
  260382. sc neg e neg e xl}{xl P P}ie 1 1 S dv o
  260383. D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  260384. %%EndPros
  260385. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  260386. 790 630 545 1085 SPn/origstk x
  260387. 65535 65535 65535 sBg
  260388. 0 0 0 C
  260389. 2270 5374 M
  260390. 2250 5386 l
  260391. 2250 4774 l
  260392. 2270 4786 l
  260393. 2342 5338 M
  260394. 2322 5338 t
  260395. 2322 4822 l
  260396. 2342 4822 l
  260397. 2780 5668 M
  260398. 2780 5692 l
  260399. 2250 5386 l
  260400. 2270 5374 l
  260401. 3290 5374 M
  260402. 3300 5380 l
  260403. 3301 5391 l
  260404. 2780 5692 l
  260405. 2780 5668 l
  260406. 3223 5329 M
  260407. 3233 5347 l
  260408. 2785 5606 l
  260409. 2775 5588 l
  260410. 3290 4786 M
  260411. 3300 4780 l
  260412. 3310 4788 l
  260413. 3310 5372 l
  260414. 3300 5380 l
  260415. 3290 5374 l
  260416. 2780 4492 M
  260417. 2780 4468 l
  260418. 3301 4769 l
  260419. 3300 4780 l
  260420. 3290 4786 l
  260421. 2775 4572 M
  260422. 2785 4554 l
  260423. 3233 4813 l
  260424. 3223 4831 l
  260425. 80 4468 M
  260426. 2780 4492 l
  260427. 2270 4786 l
  260428. 2250 4774 l
  260429. 3867 5553 M
  260430. 3871 5565 l
  260431. 3863 5573 l
  260432. 3301 5391 l
  260433. 3300 5380 l
  260434. 3310 5372 l
  260435. 4211 5079 M
  260436. 4235 5079 l
  260437. 3882 5566 l
  260438. 3871 5565 l
  260439. 3867 5553 l
  260440. 4126 507w
  260441. 4142 5085 l
  260442. 3851 5486 l
  260443. 3835 5474 l
  260444. 3939 4705 M
  260445. 3955 4693 l
  260446. 4235 5079 l
  260447. 4211 5079 l
  260448. 3756 4620 M
  260449. 3762 4640 l
  260450. 3310 4788 l
  260451. 3300 4780 l
  260452. 3301 4769 l
  260453. 4066 6126 M
  260454. 4050 6146 l
  260455. 3863 5573 l
  260456. 71 5565 l
  260457. 3882 5566 l
  260458. 4665 6126 M
  260459. 4651 6146 l
  260460. 4050 6146 l
  260461. 4066 6126 l
  260462. 4838 6571 M
  260463. 4820 6579 l
  260464. 4651 6146 l
  260465. 4665 6126 l
  260466. count origstk sub{P}rp end
  260467. chemsave restore
  260468.     Helvetica
  260469.     Helvetica
  260470. 3ff3f
  260471. ff3wf
  260472. 3DfUf
  260473. 3f33f
  260474. f3ff33"
  260475. ff33ff3f33"3"
  260476. "f"3f3"
  260477. 3f3ff33
  260478. 3f33ff
  260479. "33wf33"
  260480. 3    "3"33"
  260481. 3ff"3fw
  260482. f"33"
  260483. 3wf33"3f3
  260484. f3ff33
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  260494. f33f"33ff
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  260499. 3    f"3"3"
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  260504. 33f["fDf3ff3f3"3
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  261016. Untitled JOC Document-5
  261017. count
  261018. currentpoint 192837465
  261019. currentpoint
  261020. save/chemsave exch def
  261021. %%BeginProcSet: chemdict30 24 10
  261022. % ChemDraw Laser Prep
  261023. % Copyright 1
  261024. Untitled JOC Document-6
  261025. count
  261026. currentpoint 192837465
  261027. currentpoint
  261028. save/chemsave exch def
  261029. %%BeginProcSet: chemdict30 24 10
  261030. % ChemDraw Laser Prep
  261031. % Copyright 1
  261032. 986-1993, Cambridge Scientific Computing, Inc.
  261033. userdict/chemdict30 210 dict put
  261034. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  261035. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P
  261036. /pop L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  261037. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  261038. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst 
  261039. R/sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  261040. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  261041. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  261042. /sRmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261043. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261044. 0 cw 2 dv xl
  261045. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  261046. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  261047. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  261048. St 16 and 0 ne{
  261049. 2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  261050. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  261051. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  261052. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  261053. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  261054. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  261055. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180
  261056.  aA a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  261057. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  261058. P P}{sq at 2
  261059. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  261060. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  261061.  .35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  261062. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  261063. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  261064. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 
  261065. SA OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  261066. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  261067. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  261068. 21 -10 27 -8 27 0 cv
  261069. 27 8 21 10 9 6 cv
  261070. -3 2 -3 -2 9 -6 cv
  261071. cp}b/DLB{0 0 M -4.8 4.8 l
  261072. -8 8 -9.6 12 -9.6 16.8 cv
  261073. -9.6 
  261074. 21.6 -8 24.6 -4.8 25.8 cv
  261075. -1.6 27 1.6 27 4.8 25.8 cv
  261076. 8 24.6 9.6 21.6 9.6 16.8 cv
  261077. 9.6 12 8 8 4.8 4.8 cv
  261078. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  261079. 0 Y X Y rO ac
  261080. X Y X 0 rO ac
  261081. X 0 0 0 rO ac
  261082. 0 0 0 Y rO ac
  261083. cp}b/Rc{0 0 p M
  261084. 0 Y p l
  261085. X Y p l
  261086. X 0 p l
  261087. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  261088. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT
  261089.  idtransform
  261090. m D 0 lt{n}if sq n D
  261091. CMT dtransform idtransform
  261092. e 2 m e
  261093. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  261094. 32 -0.5 0.5{gs
  261095. 13.5 0 xl
  261096. D 32 s 64 dv 13.5 m D 7 m 24 dv
  261097. -13.5 0 xl
  261098. gr}for
  261099. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  261100. 32 -0.5 0.5{gs
  261101. D 32 s 64 dv 0.65 m D
  261102. gr}for
  261103. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  261104. 32 -0.5 0.5{gs
  261105. D 32 s 64 dv D
  261106. gr}for
  261107. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  261108. 32 -0.5 0.5{gs
  261109. 0 13.5 xl
  261110. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  261111. 0 -13.5 xl
  261112. DLB f
  261113. gr}for
  261114. DLB SM
  261115.  st}{DLB grf}ie}b/gRr{sh{sRmp
  261116. 32 -0.5 0.5{gs
  261117. X 2 dv Y 2 dv xl
  261118. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  261119. X -2 dv Y -2 dv xl
  261120. gr}for
  261121. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  261122. 32 -0.5 0.5{gs
  261123. X 2 dv Y 2 dv xl
  261124. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  261125. X -2 dv Y -2 dv xl
  261126. gr}for
  261127. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  261128. rev{1 -1 sc}if
  261129. 0 lW 2 m xl
  261130. D SA OA
  261131. rad 0 xl
  261132. 180 ro
  261133. 0 lW 2 m xl
  261134. SA OA}b/Aos{X Y M S
  261135. M cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  261136. o 0 lt o 0 lt ne/rev x
  261137. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  261138. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  261139. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  261140. lp 0 p M
  261141. 0 0 0 Y lp ac
  261142. 0 Y 2 dv lp neg o lp ac
  261143. 0 Y 2 dv 0 Y lp ac
  261144. 0 Y lp Y lp ac
  261145. X lp s 0 p M
  261146. X 0 X Y lp ac
  261147. X Y 2 dv X lp a o lp ac
  261148. X Y 2 dv X Y lp ac
  261149. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180
  261150.  pA s 180 pA a arc st
  261151. np X Y s Y 2 dv
  261152. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  261153. rO D rlineto
  261154. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  261155. rO lW -2 dv a Y lW 2 dv a rO a p l
  261156. lW -2 dv Y lW 2 dv a p l
  261157. 0 Y p l X Y p l X 0 p l cp f
  261158. 0 0 p M
  261159. 0 Y p l
  261160. X Y p l
  261161. X 0 p l cp
  261162. SM st}{Rr SM st}{rO Y p M rO rO xl
  261163. 0 Y X Y rO ac
  261164. X Y X 0 rO ac
  261165. X 0 0 0 rO ac
  261166. rO neg D xl X Y 0 Y rO ac
  261167. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  261168. -1 -1 sc LB whf}{Asc gs gLB gr
  261169. -0.4 
  261170. -0.4 sc LB whf}{Asc LB gs whf gr
  261171. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  261172. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  261173. gs 3.6 12 sc gOv gr
  261174. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  261175. gs 3.6 12 sc Cr whf gr
  261176. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  261177. 0 -1 p M
  261178. 0 0 1 0 1 ac
  261179. 8 0 8 1 1 ac
  261180. 8 0 16 0 1 ac
  261181. 16 0 16 -1 1 ac
  261182. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  261183. 2 dv D sc
  261184. 1 0 M -1 0 l
  261185. 0 1 M 0 -1 
  261186. Ast}{XY D X Y dt 0 0 M SM cpt xl
  261187. 2 dv D sc
  261188. 1 0 M -1 0 l
  261189. Ast}{4.5 Aos
  261190. 1 0 M -1 0 l
  261191. 0 1 M 0 -1 l
  261192. 2 0 M 0 0 2 0 360 arc
  261193. Ast}{4.5 Aos
  261194. 1 0 M -1 0 l
  261195. 2 0 M 0 0 2 0 360 arc
  261196. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  261197. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  261198. 1 -1 M -1 -1 l
  261199. 0 2 M 0 -2 l
  261200. Ast}{5 Aos
  261201. 1 -1 M -1 -1 l
  261202. 1 1 M -1 1 l
  261203. 0 2 M 0 -2 l
  261204. Ast}{4.5 Aos
  261205. 1 0 M -1 0 l
  261206. 0 1 M 0 -1 l
  261207. Ast}{4.5 Aos
  261208. 1 0 M -1 0 l
  261209. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -
  261210. 1 sc DLB gs whf gr
  261211. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  261212. gs 3.6 12 sc Cr whf gr
  261213. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  261214. gs 3.6 12 sc Cr blf gr
  261215. ZLB whf}{Asc LB gs whf gr
  261216. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  261217. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  261218. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  261219. e 2 ix
  261220.  a}b/PT{D 2 4 gi al P OP D 1 sc
  261221. o length 6 gt{P 6 g}{e P 8 dv}ie
  261222. D lW 2 m lt{P lW 2 m}if
  261223. 0 e p
  261224. 0 0 p
  261225. 3 -1 r s 3 1 r e s e
  261226. 0 0 p M 1 0 p l
  261227. 0 0 p ap M 1 0 p ap l
  261228. e n e n
  261229. 0 0 p ap M 1 0 p ap l
  261230. P P}b
  261231. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  261232. cvi D 0 eq{P 1}if/nH x
  261233. D hS nH m s
  261234. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  261235. bW 2 dv/bd x
  261236. lW 2 dv e D NH e{D bd p M bd n p l}for
  261237. st gr}{gs 12 OB np
  261238. lW 2 dv 0 xl NH 1 sc
  261239. bW 2 dv 
  261240. wF m nH 1 a dv/bd x
  261241. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  261242. np 0 lW 2 dv o o n p M p l bW 2 dv
  261243. wF m o o p l n p l
  261244. cp f gr}{P}{gs 12 OB/bL x
  261245. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  261246. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  261247. bL nSq 2 m dv D sc
  261248. nSq{.135  .667 .865  .667 1 0 rcurveto
  261249. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  261250. np 0 lW 2 dv o o n p M p l bW 2 dv
  261251. wF m o o p l n p l
  261252. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi
  261253.  al P
  261254. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  261255. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  261256. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  261257. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  261258. 5 -1 r dv neg e 5 -1 r dv neg e
  261259. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  261260. #    ]    a
  261261. $    Y    ]
  261262. %    V    Y
  261263. &    R    V
  261264. '    N    R
  261265. (    K    N
  261266. %%EndProcSet
  261267. 37 75 19 4 50 c
  261268. hemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  261269. 3530 720 15 990 SPn/origstk x
  261270. 65535 65535 65535 sBg
  261271. 0 0 0 C
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  261288. 3118 5688 1734 5688 2 Ar
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  261516. count origstk sub{P}rp end
  261517. chemsave restore
  261518.     Helvetica
  261519. Times
  261520.     1)TosMIC
  261521.    NaH
  261522.    Et
  261523. O/DMSO
  261524.    THF
  261525. 85-110
  261526. CO2R3
  261527. CO2R3j
  261528. CO2R3
  261529. 1)TosMIC
  261530.    NaH
  261531.    Et2O/DMSO
  261532.    THF
  261533. ClCO2R3
  261534. 85-110oC
  261535.     Helvetica
  261536. Times
  261537. Untitled Document-9
  261538. count
  261539. currentpoint 192837465
  261540. currentpoint
  261541. save/chemsave exch def
  261542. %%BeginProcSet: chemdict30 24 10
  261543. % ChemDraw Laser Prep
  261544. % Copyright 1986-
  261545. 986-1993, Cambridge Scientific Computing, Inc.
  261546. userdict/chemdict30 210 dict put
  261547. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  261548. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P
  261549. /pop L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  261550. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  261551. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst 
  261552. R/sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  261553. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  261554. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  261555. /sRmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261556. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261557. 0 cw 2 dv xl
  261558. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  261559. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  261560. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  261561. St 16 and 0 ne{
  261562. 2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  261563. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  261564. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  261565. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  261566. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  261567. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  261568. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180
  261569.  aA a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  261570. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  261571. P P}{sq at 2
  261572. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  261573. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  261574.  .35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  261575. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  261576. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  261577. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 
  261578. SA OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  261579. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  261580. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  261581. 21 -10 27 -8 27 0 cv
  261582. 27 8 21 10 9 6 cv
  261583. -3 2 -3 -2 9 -6 cv
  261584. cp}b/DLB{0 0 M -4.8 4.8 l
  261585. -8 8 -9.6 12 -9.6 16.8 cv
  261586. -9.6 
  261587. 21.6 -8 24.6 -4.8 25.8 cv
  261588. -1.6 27 1.6 27 4.8 25.8 cv
  261589. 8 24.6 9.6 21.6 9.6 16.8 cv
  261590. 9.6 12 8 8 4.8 4.8 cv
  261591. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  261592. 0 Y X Y rO ac
  261593. X Y X 0 rO ac
  261594. X 0 0 0 rO ac
  261595. 0 0 0 Y rO ac
  261596. cp}b/Rc{0 0 p M
  261597. 0 Y p l
  261598. X Y p l
  261599. X 0 p l
  261600. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  261601. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT
  261602.  idtransform
  261603. m D 0 lt{n}if sq n D
  261604. CMT dtransform idtransform
  261605. e 2 m e
  261606. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  261607. 32 -0.5 0.5{gs
  261608. 13.5 0 xl
  261609. D 32 s 64 dv 13.5 m D 7 m 24 dv
  261610. -13.5 0 xl
  261611. gr}for
  261612. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  261613. 32 -0.5 0.5{gs
  261614. D 32 s 64 dv 0.65 m D
  261615. gr}for
  261616. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  261617. 32 -0.5 0.5{gs
  261618. D 32 s 64 dv D
  261619. gr}for
  261620. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  261621. 32 -0.5 0.5{gs
  261622. 0 13.5 xl
  261623. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  261624. 0 -13.5 xl
  261625. DLB f
  261626. gr}for
  261627. DLB SM
  261628.  st}{DLB grf}ie}b/gRr{sh{sRmp
  261629. 32 -0.5 0.5{gs
  261630. X 2 dv Y 2 dv xl
  261631. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  261632. X -2 dv Y -2 dv xl
  261633. gr}for
  261634. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  261635. 32 -0.5 0.5{gs
  261636. X 2 dv Y 2 dv xl
  261637. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  261638. X -2 dv Y -2 dv xl
  261639. gr}for
  261640. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  261641. rev{1 -1 sc}if
  261642. 0 lW 2 m xl
  261643. D SA OA
  261644. rad 0 xl
  261645. 180 ro
  261646. 0 lW 2 m xl
  261647. SA OA}b/Aos{X Y M S
  261648. M cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  261649. o 0 lt o 0 lt ne/rev x
  261650. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  261651. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  261652. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  261653. lp 0 p M
  261654. 0 0 0 Y lp ac
  261655. 0 Y 2 dv lp neg o lp ac
  261656. 0 Y 2 dv 0 Y lp ac
  261657. 0 Y lp Y lp ac
  261658. X lp s 0 p M
  261659. X 0 X Y lp ac
  261660. X Y 2 dv X lp a o lp ac
  261661. X Y 2 dv X Y lp ac
  261662. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180
  261663.  pA s 180 pA a arc st
  261664. np X Y s Y 2 dv
  261665. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  261666. rO D rlineto
  261667. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  261668. rO lW -2 dv a Y lW 2 dv a rO a p l
  261669. lW -2 dv Y lW 2 dv a p l
  261670. 0 Y p l X Y p l X 0 p l cp f
  261671. 0 0 p M
  261672. 0 Y p l
  261673. X Y p l
  261674. X 0 p l cp
  261675. SM st}{Rr SM st}{rO Y p M rO rO xl
  261676. 0 Y X Y rO ac
  261677. X Y X 0 rO ac
  261678. X 0 0 0 rO ac
  261679. rO neg D xl X Y 0 Y rO ac
  261680. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  261681. -1 -1 sc LB whf}{Asc gs gLB gr
  261682. -0.4 
  261683. -0.4 sc LB whf}{Asc LB gs whf gr
  261684. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  261685. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  261686. gs 3.6 12 sc gOv gr
  261687. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  261688. gs 3.6 12 sc Cr whf gr
  261689. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  261690. 0 -1 p M
  261691. 0 0 1 0 1 ac
  261692. 8 0 8 1 1 ac
  261693. 8 0 16 0 1 ac
  261694. 16 0 16 -1 1 ac
  261695. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  261696. 2 dv D sc
  261697. 1 0 M -1 0 l
  261698. 0 1 M 0 -1 
  261699. Ast}{XY D X Y dt 0 0 M SM cpt xl
  261700. 2 dv D sc
  261701. 1 0 M -1 0 l
  261702. Ast}{4.5 Aos
  261703. 1 0 M -1 0 l
  261704. 0 1 M 0 -1 l
  261705. 2 0 M 0 0 2 0 360 arc
  261706. Ast}{4.5 Aos
  261707. 1 0 M -1 0 l
  261708. 2 0 M 0 0 2 0 360 arc
  261709. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  261710. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  261711. 1 -1 M -1 -1 l
  261712. 0 2 M 0 -2 l
  261713. Ast}{5 Aos
  261714. 1 -1 M -1 -1 l
  261715. 1 1 M -1 1 l
  261716. 0 2 M 0 -2 l
  261717. Ast}{4.5 Aos
  261718. 1 0 M -1 0 l
  261719. 0 1 M 0 -1 l
  261720. Ast}{4.5 Aos
  261721. 1 0 M -1 0 l
  261722. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -
  261723. 1 sc DLB gs whf gr
  261724. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  261725. gs 3.6 12 sc Cr whf gr
  261726. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  261727. gs 3.6 12 sc Cr blf gr
  261728. ZLB whf}{Asc LB gs whf gr
  261729. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  261730. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  261731. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  261732. e 2 ix
  261733.  a}b/PT{D 2 4 gi al P OP D 1 sc
  261734. o length 6 gt{P 6 g}{e P 8 dv}ie
  261735. D lW 2 m lt{P lW 2 m}if
  261736. 0 e p
  261737. 0 0 p
  261738. 3 -1 r s 3 1 r e s e
  261739. 0 0 p M 1 0 p l
  261740. 0 0 p ap M 1 0 p ap l
  261741. e n e n
  261742. 0 0 p ap M 1 0 p ap l
  261743. P P}b
  261744. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  261745. cvi D 0 eq{P 1}if/nH x
  261746. D hS nH m s
  261747. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  261748. bW 2 dv/bd x
  261749. lW 2 dv e D NH e{D bd p M bd n p l}for
  261750. st gr}{gs 12 OB np
  261751. lW 2 dv 0 xl NH 1 sc
  261752. bW 2 dv 
  261753. wF m nH 1 a dv/bd x
  261754. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  261755. np 0 lW 2 dv o o n p M p l bW 2 dv
  261756. wF m o o p l n p l
  261757. cp f gr}{P}{gs 12 OB/bL x
  261758. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  261759. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  261760. bL nSq 2 m dv D sc
  261761. nSq{.135  .667 .865  .667 1 0 rcurveto
  261762. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  261763. np 0 lW 2 dv o o n p M p l bW 2 dv
  261764. wF m o o p l n p l
  261765. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi
  261766.  al P
  261767. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  261768. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  261769. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  261770. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  261771. 5 -1 r dv neg e 5 -1 r dv neg e
  261772. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  261773. %%EndProcSet
  261774. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  261775. 2275 490 558 1170 SPn/origstk x
  261776. 65535 65535 65535 sBg
  261777. 0 0 0 C
  261778. 2320 6234 M
  261779. 2300 6246 l
  261780. 2300 5634 l
  261781. 2320 5646 l
  261782. 2830 6528 M
  261783. 2830 6552 l
  261784. 2300 6246 l
  261785. 2320 6234 l
  261786. 3340 6234 M
  261787. 3360 6246 l
  261788. 2830 6552 l
  261789. 2830 6528 l
  261790. 3340 5646 M
  261791. 3360 
  261792. 5634 l
  261793. 3360 6246 l
  261794. 3340 6234 l
  261795. 3268 5682 M
  261796. 3288 5682 l
  261797. 3288 6198 l
  261798. 3268 6198 l
  261799. 2830 5352 M
  261800. 2830 5328 l
  261801. 3360 5634 l
  261802. 3340 5646 l
  261803. 2830 5328 M
  261804. 2830 5352 l
  261805. 2320 5646 l
  261806. 2300 5634 l
  261807. 4440 6214 M
  261808. 4420 6226 l
  261809. 4420 5614 l
  261810. 4440 5626 l
  261811. 4512 6178 M
  261812. 4492 6178 l
  261813. 4492 5662 l
  261814. 4512 5662 l
  261815. 4950 6508 M
  261816. 4950 6532 l
  261817. 4420 6226 l
  261818. 4440 6214 l
  261819. 5460 6214 M
  261820. 5470 6220 l
  261821. 5470 6232 l
  261822. 4950 6532 l
  261823. 4950 6508 l
  261824. 5393 6169 M
  261825. 5403 6187 l
  261826. 4955 6446 l
  261827. 4945 6428 l
  261828. 5460 5626 M
  261829. 5470 5620 l
  261830. 5480 5626 l
  261831. 5480 6214 l
  261832. 5470 6220 l
  261833. 5460 6214 l
  261834. 4950 5332 M
  261835. 4950 5308 l
  261836. 5471 5609 l
  261837. 5470 5620 l
  261838. 5460 5626 l
  261839. 4945 5412 M
  261840. 4955 5394 l
  261841. 5403 5653 l
  261842. 5393 5671 l
  261843. 4950 5308 M
  261844. 4950 5332 l
  261845. 4440 5626 l
  261846. 4420 5614 l
  261847. 5950 5408 M
  261848. 5958 5426 l
  261849. 5480 5626 l
  261850. 5470 5620 l
  261851. 5471 5609 l
  261852. 6013 4904 M
  261853. 6033 4904 l
  261854. 6033 5276 l
  261855. 6013 5276 l
  261856. 5897 6459 M
  261857. 5887 6477 l
  261858. 5470 6232 l
  261859. 5470 6220 l
  261860. 5480 6214 l
  261861. 8990 5820 7350 5820 2 Ar
  261862. 9580 6074 M
  261863. 9560 6086 l
  261864. 9560 5474 l
  261865. 9580 5486 l
  261866. 10090 6368 M
  261867. 10090 6392 l
  261868. 9560 6086 l
  261869. 9580 6074 l
  261870. 10600 6074 M
  261871. 10610 6080 l
  261872. 10610 6092 l
  261873. 10090 6392 l
  261874. 10090 6368 l
  261875. 10600 5486 M
  261876. 10620 5474 l
  261877. 10620 6074 l
  261878. 10610 6080 l
  261879. 10600 6074 l
  261880. 10090 5192 M
  261881. 10090 5168 l
  261882. 10620 5474 l
  261883. 10600 5486 l
  261884. 10090 5168 M
  261885. 10090 5192 l
  261886. 9580 5486 l
  261887. 9560 5474 l
  261888. 10983 5198 M
  261889. 10993 5216 l
  261890. 10580 5469 l
  261891. 10570 5451 l
  261892. 11021 5260 M
  261893. 11031 5278 l
  261894. 10615 5531 l
  261895. 10605 5513 l
  261896. 11039 6
  261897. 291 M
  261898. 11029 6309 l
  261899. 10610 6092 l
  261900. 10610 6080 l
  261901. 10620 6074 l
  261902. count origstk sub{P}rp end
  261903. chemsave restore
  261904.     Helvetica
  261905. Times
  261906. -20 -> r.t.
  261907. -20 -> r.t.
  261908.     Helvetica
  261909. Times
  261910. Untitled Document-1
  261911. count
  261912. currentpoint 192837465
  261913. currentpoint
  261914. save/chemsave exch def
  261915. %%BeginProcSet: chemdict30 24 10
  261916. % ChemDraw Laser Prep
  261917. % Copyright 1986-
  261918. 1993, Cambridge Scientific Computing, Inc.
  261919. userdict/chemdict30 210 dict put
  261920. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  261921. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  261922.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  261923. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  261924. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  261925.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  261926. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  261927. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  261928. x}b/sRm
  261929. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261930. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  261931. 0 cw 2 dv xl
  261932. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  261933. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  261934. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  261935. St 16 and 0 ne{2 ix
  261936.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  261937. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  261938. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  261939. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  261940. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  261941. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  261942. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  261943. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  261944. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  261945. P P}{sq at 2
  261946. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  261947. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  261948. l w .35
  261949.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  261950. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  261951. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  261952. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  261953. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  261954. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  261955. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  261956. 21 -10 27 -8 27 0 cv
  261957. 27 8 21 10 9 6 cv
  261958. -3 2 -3 -2 9 -6 cv
  261959. cp}b/DLB{0 0 M -4.8 4.8 l
  261960. -8 8 -9.6 12 -9.6 16.8 cv
  261961. -9.6 21.6
  261962.  -8 24.6 -4.8 25.8 cv
  261963. -1.6 27 1.6 27 4.8 25.8 cv
  261964. 8 24.6 9.6 21.6 9.6 16.8 cv
  261965. 9.6 12 8 8 4.8 4.8 cv
  261966. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  261967. 0 Y X Y rO ac
  261968. X Y X 0 rO ac
  261969. X 0 0 0 rO ac
  261970. 0 0 0 Y rO ac
  261971. cp}b/Rc{0 0 p M
  261972. 0 Y p l
  261973. X Y p l
  261974. X 0 p l
  261975. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  261976. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  261977. ransform
  261978. m D 0 lt{n}if sq n D
  261979. CMT dtransform idtransform
  261980. e 2 m e
  261981. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  261982. 32 -0.5 0.5{gs
  261983. 13.5 0 xl
  261984. D 32 s 64 dv 13.5 m D 7 m 24 dv
  261985. -13.5 0 xl
  261986. gr}for
  261987. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  261988. 32 -0.5 0.5{gs
  261989. D 32 s 64 dv 0.65 m D
  261990. gr}for
  261991. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  261992. 32 -0.5 0.5{gs
  261993. D 32 s 64 dv D
  261994. gr}for
  261995. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  261996. 32 -0.5 0.5{gs
  261997. 0 13.5 xl
  261998. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  261999. 0 -13.5 xl
  262000. DLB f
  262001. gr}for
  262002. DLB SM st}
  262003. {DLB grf}ie}b/gRr{sh{sRmp
  262004. 32 -0.5 0.5{gs
  262005. X 2 dv Y 2 dv xl
  262006. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262007. X -2 dv Y -2 dv xl
  262008. gr}for
  262009. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  262010. 32 -0.5 0.5{gs
  262011. X 2 dv Y 2 dv xl
  262012. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262013. X -2 dv Y -2 dv xl
  262014. gr}for
  262015. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  262016. rev{1 -1 sc}if
  262017. 0 lW 2 m xl
  262018. D SA OA
  262019. rad 0 xl
  262020. 180 ro
  262021. 0 lW 2 m xl
  262022. SA OA}b/Aos{X Y M SM cp
  262023. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  262024. o 0 lt o 0 lt ne/rev x
  262025. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  262026. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  262027. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  262028. lp 0 p M
  262029. 0 0 0 Y lp ac
  262030. 0 Y 2 dv lp neg o lp ac
  262031. 0 Y 2 dv 0 Y lp ac
  262032. 0 Y lp Y lp ac
  262033. X lp s 0 p M
  262034. X 0 X Y lp ac
  262035. X Y 2 dv X lp a o lp ac
  262036. X Y 2 dv X Y lp ac
  262037. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  262038. s 180 pA a arc st
  262039. np X Y s Y 2 dv
  262040. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  262041. rO D rlineto
  262042. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  262043. rO lW -2 dv a Y lW 2 dv a rO a p l
  262044. lW -2 dv Y lW 2 dv a p l
  262045. 0 Y p l X Y p l X 0 p l cp f
  262046. 0 0 p M
  262047. 0 Y p l
  262048. X Y p l
  262049. X 0 p l cp
  262050. SM st}{Rr SM st}{rO Y p M rO rO xl
  262051. 0 Y X Y rO ac
  262052. X Y X 0 rO ac
  262053. X 0 0 0 rO ac
  262054. rO neg D xl X Y 0 Y rO ac
  262055. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  262056. -1 -1 sc LB whf}{Asc gs gLB gr
  262057. -0.4 -0.4
  262058.  sc LB whf}{Asc LB gs whf gr
  262059. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  262060. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  262061. gs 3.6 12 sc gOv gr
  262062. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  262063. gs 3.6 12 sc Cr whf gr
  262064. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  262065. 0 -1 p M
  262066. 0 0 1 0 1 ac
  262067. 8 0 8 1 1 ac
  262068. 8 0 16 0 1 ac
  262069. 16 0 16 -1 1 ac
  262070. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  262071. 2 dv D sc
  262072. 1 0 M -1 0 l
  262073. 0 1 M 0 -1 l
  262074. t}{XY D X Y dt 0 0 M SM cpt xl
  262075. 2 dv D sc
  262076. 1 0 M -1 0 l
  262077. Ast}{4.5 Aos
  262078. 1 0 M -1 0 l
  262079. 0 1 M 0 -1 l
  262080. 2 0 M 0 0 2 0 360 arc
  262081. Ast}{4.5 Aos
  262082. 1 0 M -1 0 l
  262083. 2 0 M 0 0 2 0 360 arc
  262084. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  262085. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  262086. 1 -1 M -1 -1 l
  262087. 0 2 M 0 -2 l
  262088. Ast}{5 Aos
  262089. 1 -1 M -1 -1 l
  262090. 1 1 M -1 1 l
  262091. 0 2 M 0 -2 l
  262092. Ast}{4.5 Aos
  262093. 1 0 M -1 0 l
  262094. 0 1 M 0 -1 l
  262095. Ast}{4.5 Aos
  262096. 1 0 M -1 0 l
  262097. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  262098.  DLB gs whf gr
  262099. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  262100. gs 3.6 12 sc Cr whf gr
  262101. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  262102. gs 3.6 12 sc Cr blf gr
  262103. ZLB whf}{Asc LB gs whf gr
  262104. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  262105. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  262106. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  262107. e 2 ix a}b
  262108. /PT{D 2 4 gi al P OP D 1 sc
  262109. o length 6 gt{P 6 g}{e P 8 dv}ie
  262110. D lW 2 m lt{P lW 2 m}if
  262111. 0 e p
  262112. 0 0 p
  262113. 3 -1 r s 3 1 r e s e
  262114. 0 0 p M 1 0 p l
  262115. 0 0 p ap M 1 0 p ap l
  262116. e n e n
  262117. 0 0 p ap M 1 0 p ap l
  262118. P P}b
  262119. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  262120. cvi D 0 eq{P 1}if/nH x
  262121. D hS nH m s
  262122. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  262123. bW 2 dv/bd x
  262124. lW 2 dv e D NH e{D bd p M bd n p l}for
  262125. st gr}{gs 12 OB np
  262126. lW 2 dv 0 xl NH 1 sc
  262127. bW 2 dv wF m
  262128.  nH 1 a dv/bd x
  262129. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  262130. np 0 lW 2 dv o o n p M p l bW 2 dv
  262131. wF m o o p l n p l
  262132. cp f gr}{P}{gs 12 OB/bL x
  262133. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  262134. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  262135. bL nSq 2 m dv D sc
  262136. nSq{.135  .667 .865  .667 1 0 rcurveto
  262137. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  262138. np 0 lW 2 dv o o n p M p l bW 2 dv
  262139. wF m o o p l n p l
  262140. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  262141. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  262142. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  262143. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  262144. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  262145. 5 -1 r dv neg e 5 -1 r dv neg e
  262146. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  262147. %%EndProcSet
  262148. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  262149. 2975 1030 118 985 SPn/origstk x
  262150. 65535 65535 65535 sBg
  262151. 0 0 0 C
  262152. 1560 4954 M
  262153. 1540 4966 l
  262154. 1540 4367 l
  262155. 1550 4360 l
  262156. 1560 4366 l
  262157. 2070 5248 M
  262158. 2070 5272 l
  262159. 1540 4966 l
  262160. 1560 4954 l
  262161. 0 4954 M
  262162. 2600 4966 l
  262163. 2070 5272 l
  262164. 2070 5248 l
  262165. 2580 4366 M
  262166. 2600 4354 l
  262167. 2600 4966 l
  262168. 2580 4954 l
  262169. 2508 4402 M
  262170. 2528 4402 l
  262171. 2528 4918 l
  262172. 2508 4918 l
  262173. 2070 4072 M
  262174. 2070 4048 l
  262175. 2600 4354 l
  262176. 2580 4366 l
  262177. 2070 4048 M
  262178. 2070 4072 l
  262179. 1560 4366 l
  262180. 1550 4360 l
  262181. 1551 4348 l
  262182. 1078 4154 M
  262183. 1138 4050 l
  262184. 1551 4348 l
  262185. 1550 4360 l
  262186. 1540 4367 l
  262187. f[1 4 1507 4987 1120 5231 ]Bd
  262188. 4850 5044 M
  262189. 4830 5056 l
  262190. 4830 4457 l
  262191. 4840 4450 l
  262192. 4850 4456 l
  262193. 5360 5338 M
  262194. 5360 5362 l
  262195. 4830 5056 l
  262196.  5044 l
  262197. 5870 5044 M
  262198. 5890 5056 l
  262199. 5360 5362 l
  262200. 5360 5338 l
  262201. 5870 4456 M
  262202. 5890 4444 l
  262203. 5890 5056 l
  262204. 5870 5044 l
  262205. 5360 4162 M
  262206. 5360 4138 l
  262207. 5890 4444 l
  262208. 5870 4456 l
  262209. 5360 4138 M
  262210. 5360 4162 l
  262211. 4850 4456 l
  262212. 4840 4450 l
  262213. 4841 4438 l
  262214. 4370 4245 M
  262215. 4430 4141 l
  262216. 4841 4438 l
  262217. 4840 4450 l
  262218. 4830 4457 l
  262219. f[1 4 4797 5077 4410 5322 ]Bd
  262220. [1 9 5880 4450 6286 4182 ]Bd
  262221. [1 9 5880 5050 6295 5308 ]Bd
  262222. 9790 5064 M
  262223. 9770 5076 l
  262224. 9770 4477 l
  262225. 9780 4470 l
  262226. 9790 4476 l
  262227. 10300 5358 M
  262228. 10300 
  262229. 5382 l
  262230. 9770 5076 l
  262231. 9790 5064 l
  262232. 10810 5064 M
  262233. 10830 5076 l
  262234. 10300 5382 l
  262235. 10300 5358 l
  262236. 10810 4476 M
  262237. 10830 4464 l
  262238. 10830 5076 l
  262239. 10810 5064 l
  262240. 10738 4512 M
  262241. 10758 4512 l
  262242. 10758 5028 l
  262243. 10738 5028 l
  262244. 10300 4182 M
  262245. 10300 4158 l
  262246. 10830 4464 l
  262247. 10810 4476 l
  262248. 10300 4158 M
  262249. 10300 4182 l
  262250. 9790 4476 l
  262251. 9780 4470 l
  262252. 9781 4458 l
  262253. 9310 4265 M
  262254. 9370 4161 l
  262255. 9781 4458 l
  262256. 9780 4470 l
  262257. 9770 4477 l
  262258. f[1 4 9737 5097 9350 5342 ]Bd
  262259. [1 9 10820 4470 11226 4202 ]Bd
  262260. 3930 7124 M
  262261. 3910 
  262262. 7136 l
  262263. 3910 6537 l
  262264. 3920 6530 l
  262265. 3930 6536 l
  262266. 4440 7418 M
  262267. 4440 7442 l
  262268. 3910 7136 l
  262269. 3930 7124 l
  262270. 4950 7124 M
  262271. 4960 7130 l
  262272. 4961 7141 l
  262273. 4440 7442 l
  262274. 4440 7418 l
  262275. 4950 6536 M
  262276. 4960 6530 l
  262277. 4970 6538 l
  262278. 4970 7122 l
  262279. 4960 7130 l
  262280. 4950 7124 l
  262281. 4440 6242 M
  262282. 4440 6218 l
  262283. 4961 6519 l
  262284. 4960 6530 l
  262285. 4950 6536 l
  262286. 4440 6218 M
  262287. 4440 6242 l
  262288. 3930 6536 l
  262289. 3920 6530 l
  262290. 3921 6518 l
  262291. 3450 6325 M
  262292. 3510 6221 l
  262293. 3921 6518 l
  262294. 3920 6530 l
  262295. 3910 6537 l
  262296. f[1 4 3877 7157 3490 7402 ]Bd
  262297. 5527 7
  262298. 303 M
  262299. 5531 7315 l
  262300. 5522 7323 l
  262301. 4961 7141 l
  262302. 4960 7130 l
  262303. 4970 7122 l
  262304. 5506 7220 M
  262305. 5500 7240 l
  262306. 5029 7088 l
  262307. 5035 7068 l
  262308. 5798 6930 M
  262309. 5814 6942 l
  262310. 5542 7317 l
  262311. 5531 7315 l
  262312. 5527 7303 l
  262313. 5527 6356 M
  262314. 5535 6332 l
  262315. 5814 6717 l
  262316. 5798 6729 l
  262317. 5535 6332 M
  262318. 5527 6356 l
  262319. 4970 6538 l
  262320. 4960 6530 l
  262321. 4961 6519 l
  262322. 5500 6419 M
  262323. 5506 6439 l
  262324. 5035 6592 l
  262325. 5029 6572 l
  262326. 5649 7785 M
  262327. 5629 7789 l
  262328. 5522 7323 l
  262329. 5531 7315 l
  262330. 5542 7317 l
  262331. 3830 4720 2930 4720 2 Ar
  262332. 8290 4720 7070 4720 2 Ar
  262333. 170 6579 530 6579 2 Ar
  262334. count origstk sub{P}rp end
  262335. chemsave restore
  262336.     Helvetica
  262337. Times
  262338. a: 1) PhSCl
  262339. , DCM 20min 2) Oxone, H
  262340. O, MeOH
  262341. b: DBU, DCM 1h
  262342. c: 1) CNCH
  262343. Et, THF, rt  2)t-BuOK, THF rt
  262344. >CHMD
  262345. CO2Et&
  262346. CO2Et
  262347. CO2EtF
  262348. CO2Et
  262349. SO2Ph.
  262350. CO2Et6
  262351. CO2Et+
  262352. SO2PhZ
  262353. CO2Et
  262354. CO2EtA
  262355. CO2EtC
  262356. +a: 1) PhSCl2, DCM 20min 2) Oxone, H2O, MeOH
  262357. b: DBU, DCM 1h
  262358. +c: 1) CNCH2CO2Et, THF, rt  2)t-BuOK, THF rt
  262359.     Helvetica
  262360. Times
  262361. Untitled Document-3
  262362. count
  262363. currentpoint 192837465
  262364. currentpoint
  262365. save/chemsave exch def
  262366. %%BeginProcSet: chemdict30 24 10
  262367. % ChemDraw Laser Prep
  262368. % Copyright 1986-
  262369. 1993, Cambridge Scientific Computing, Inc.
  262370. userdict/chemdict30 210 dict put
  262371. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  262372. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  262373.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  262374. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  262375. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  262376.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  262377. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  262378. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  262379. x}b/sRm
  262380. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  262381. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  262382. 0 cw 2 dv xl
  262383. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  262384. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  262385. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  262386. St 16 and 0 ne{2 ix
  262387.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  262388. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  262389. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  262390. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  262391. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  262392. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  262393. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  262394. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  262395. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  262396. P P}{sq at 2
  262397. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  262398. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  262399. l w .35
  262400.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  262401. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  262402. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  262403. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  262404. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  262405. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  262406. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  262407. 21 -10 27 -8 27 0 cv
  262408. 27 8 21 10 9 6 cv
  262409. -3 2 -3 -2 9 -6 cv
  262410. cp}b/DLB{0 0 M -4.8 4.8 l
  262411. -8 8 -9.6 12 -9.6 16.8 cv
  262412. -9.6 21.6
  262413.  -8 24.6 -4.8 25.8 cv
  262414. -1.6 27 1.6 27 4.8 25.8 cv
  262415. 8 24.6 9.6 21.6 9.6 16.8 cv
  262416. 9.6 12 8 8 4.8 4.8 cv
  262417. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  262418. 0 Y X Y rO ac
  262419. X Y X 0 rO ac
  262420. X 0 0 0 rO ac
  262421. 0 0 0 Y rO ac
  262422. cp}b/Rc{0 0 p M
  262423. 0 Y p l
  262424. X Y p l
  262425. X 0 p l
  262426. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  262427. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  262428. ransform
  262429. m D 0 lt{n}if sq n D
  262430. CMT dtransform idtransform
  262431. e 2 m e
  262432. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  262433. 32 -0.5 0.5{gs
  262434. 13.5 0 xl
  262435. D 32 s 64 dv 13.5 m D 7 m 24 dv
  262436. -13.5 0 xl
  262437. gr}for
  262438. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  262439. 32 -0.5 0.5{gs
  262440. D 32 s 64 dv 0.65 m D
  262441. gr}for
  262442. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  262443. 32 -0.5 0.5{gs
  262444. D 32 s 64 dv D
  262445. gr}for
  262446. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  262447. 32 -0.5 0.5{gs
  262448. 0 13.5 xl
  262449. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  262450. 0 -13.5 xl
  262451. DLB f
  262452. gr}for
  262453. DLB SM st}
  262454. {DLB grf}ie}b/gRr{sh{sRmp
  262455. 32 -0.5 0.5{gs
  262456. X 2 dv Y 2 dv xl
  262457. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262458. X -2 dv Y -2 dv xl
  262459. gr}for
  262460. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  262461. 32 -0.5 0.5{gs
  262462. X 2 dv Y 2 dv xl
  262463. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262464. X -2 dv Y -2 dv xl
  262465. gr}for
  262466. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  262467. rev{1 -1 sc}if
  262468. 0 lW 2 m xl
  262469. D SA OA
  262470. rad 0 xl
  262471. 180 ro
  262472. 0 lW 2 m xl
  262473. SA OA}b/Aos{X Y M SM cp
  262474. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  262475. o 0 lt o 0 lt ne/rev x
  262476. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  262477. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  262478. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  262479. lp 0 p M
  262480. 0 0 0 Y lp ac
  262481. 0 Y 2 dv lp neg o lp ac
  262482. 0 Y 2 dv 0 Y lp ac
  262483. 0 Y lp Y lp ac
  262484. X lp s 0 p M
  262485. X 0 X Y lp ac
  262486. X Y 2 dv X lp a o lp ac
  262487. X Y 2 dv X Y lp ac
  262488. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  262489. s 180 pA a arc st
  262490. np X Y s Y 2 dv
  262491. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  262492. rO D rlineto
  262493. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  262494. rO lW -2 dv a Y lW 2 dv a rO a p l
  262495. lW -2 dv Y lW 2 dv a p l
  262496. 0 Y p l X Y p l X 0 p l cp f
  262497. 0 0 p M
  262498. 0 Y p l
  262499. X Y p l
  262500. X 0 p l cp
  262501. SM st}{Rr SM st}{rO Y p M rO rO xl
  262502. 0 Y X Y rO ac
  262503. X Y X 0 rO ac
  262504. X 0 0 0 rO ac
  262505. rO neg D xl X Y 0 Y rO ac
  262506. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  262507. -1 -1 sc LB whf}{Asc gs gLB gr
  262508. -0.4 -0.4
  262509.  sc LB whf}{Asc LB gs whf gr
  262510. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  262511. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  262512. gs 3.6 12 sc gOv gr
  262513. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  262514. gs 3.6 12 sc Cr whf gr
  262515. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  262516. 0 -1 p M
  262517. 0 0 1 0 1 ac
  262518. 8 0 8 1 1 ac
  262519. 8 0 16 0 1 ac
  262520. 16 0 16 -1 1 ac
  262521. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  262522. 2 dv D sc
  262523. 1 0 M -1 0 l
  262524. 0 1 M 0 -1 l
  262525. t}{XY D X Y dt 0 0 M SM cpt xl
  262526. 2 dv D sc
  262527. 1 0 M -1 0 l
  262528. Ast}{4.5 Aos
  262529. 1 0 M -1 0 l
  262530. 0 1 M 0 -1 l
  262531. 2 0 M 0 0 2 0 360 arc
  262532. Ast}{4.5 Aos
  262533. 1 0 M -1 0 l
  262534. 2 0 M 0 0 2 0 360 arc
  262535. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  262536. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  262537. 1 -1 M -1 -1 l
  262538. 0 2 M 0 -2 l
  262539. Ast}{5 Aos
  262540. 1 -1 M -1 -1 l
  262541. 1 1 M -1 1 l
  262542. 0 2 M 0 -2 l
  262543. Ast}{4.5 Aos
  262544. 1 0 M -1 0 l
  262545. 0 1 M 0 -1 l
  262546. Ast}{4.5 Aos
  262547. 1 0 M -1 0 l
  262548. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  262549.  DLB gs whf gr
  262550. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  262551. gs 3.6 12 sc Cr whf gr
  262552. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  262553. gs 3.6 12 sc Cr blf gr
  262554. ZLB whf}{Asc LB gs whf gr
  262555. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  262556. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  262557. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  262558. e 2 ix a}b
  262559. /PT{D 2 4 gi al P OP D 1 sc
  262560. o length 6 gt{P 6 g}{e P 8 dv}ie
  262561. D lW 2 m lt{P lW 2 m}if
  262562. 0 e p
  262563. 0 0 p
  262564. 3 -1 r s 3 1 r e s e
  262565. 0 0 p M 1 0 p l
  262566. 0 0 p ap M 1 0 p ap l
  262567. e n e n
  262568. 0 0 p ap M 1 0 p ap l
  262569. P P}b
  262570. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  262571. cvi D 0 eq{P 1}if/nH x
  262572. D hS nH m s
  262573. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  262574. bW 2 dv/bd x
  262575. lW 2 dv e D NH e{D bd p M bd n p l}for
  262576. st gr}{gs 12 OB np
  262577. lW 2 dv 0 xl NH 1 sc
  262578. bW 2 dv wF m
  262579.  nH 1 a dv/bd x
  262580. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  262581. np 0 lW 2 dv o o n p M p l bW 2 dv
  262582. wF m o o p l n p l
  262583. cp f gr}{P}{gs 12 OB/bL x
  262584. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  262585. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  262586. bL nSq 2 m dv D sc
  262587. nSq{.135  .667 .865  .667 1 0 rcurveto
  262588. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  262589. np 0 lW 2 dv o o n p M p l bW 2 dv
  262590. wF m o o p l n p l
  262591. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  262592. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  262593. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  262594. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  262595. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  262596. 5 -1 r dv neg e 5 -1 r dv neg e
  262597. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  262598. %%EndProcSet
  262599. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  262600. 2390 1220 55 575 SPn/origstk x
  262601. 65535 65535 65535 sBg
  262602. 0 0 0 C
  262603. 310 4154 M
  262604. 290 4166 l
  262605. 290 3554 l
  262606. 310 3566 l
  262607. 820 4448 M
  262608. 820 4472 l
  262609. 290 4166 l
  262610. 310 4154 l
  262611. 1330 4154 M
  262612. 1350 4166 l
  262613. 820 4472 l
  262614. 820 4448 l
  262615. 1330 3566 M
  262616. 1340 3560 l
  262617. 1350 3566 l
  262618. 1350 4166 l
  262619.  4154 l
  262620. 820 3272 M
  262621. 820 3248 l
  262622. 1340 3548 l
  262623. 1340 3560 l
  262624. 1330 3566 l
  262625. 820 3248 M
  262626. 820 3272 l
  262627. 310 3566 l
  262628. 290 3554 l
  262629. 774 2778 M
  262630. 794 2778 l
  262631. 794 3280 l
  262632. 774 3280 l
  262633. 846 2778 M
  262634. 866 2778 l
  262635. 866 3280 l
  262636. 846 3280 l
  262637. 1750 3294 M
  262638. 1760 3312 l
  262639. 1350 3566 l
  262640. 1340 3560 l
  262641. 1340 3548 l
  262642. 5690 4634 M
  262643. 5670 4646 l
  262644. 5670 4034 l
  262645. 5690 4046 l
  262646. 6200 4928 M
  262647. 6200 4952 l
  262648. 5670 4646 l
  262649. 5690 4634 l
  262650. 6710 4634 M
  262651. 6730 4646 l
  262652. 6200 4952 l
  262653. 6200 4928 l
  262654. 6710 4046 M
  262655. 6720 404
  262656. 6730 4046 l
  262657. 6730 4646 l
  262658. 6710 4634 l
  262659. 6200 3752 M
  262660. 6200 3740 l
  262661. 6210 3734 l
  262662. 6720 4028 l
  262663. 6720 4040 l
  262664. 6710 4046 l
  262665. 6190 3734 M
  262666. 6200 3740 l
  262667. 6200 3752 l
  262668. 5690 4046 l
  262669. 5670 4034 l
  262670. 6190 3254 M
  262671. 6210 3254 l
  262672. 6210 3734 l
  262673. 6200 3740 l
  262674. 6190 3734 l
  262675. 6118 3254 M
  262676. 6138 3254 l
  262677. 6138 3698 l
  262678. 6118 3698 l
  262679. 5651 2906 M
  262680. 5652 2896 l
  262681. 5659 2888 l
  262682. 6105 3087 l
  262683. 6097 3105 l
  262684. 5185 3078 M
  262685. 5179 3060 l
  262686. 5636 2892 l
  262687. 5652 2896 l
  262688. 5651 2906 l
  262689. 7149 3804 M
  262690. 7159 3822 l
  262691. 6730 4046 l
  262692. 20 4040 l
  262693. 6720 4028 l
  262694. 8550 3132 M
  262695. 8550 3156 l
  262696. 8045 3469 l
  262697. 8035 3451 l
  262698. 8545 3220 M
  262699. 8555 3238 l
  262700. 8083 3530 l
  262701. 8073 3512 l
  262702. 8960 3384 M
  262703. 8950 3402 l
  262704. 8550 3156 l
  262705. 8550 3132 l
  262706. 1050 6794 M
  262707. 1030 6806 l
  262708. 1030 6194 l
  262709. 1050 6206 l
  262710. 1560 7088 M
  262711. 1560 7112 l
  262712. 1030 6806 l
  262713. 1050 6794 l
  262714. 2070 6794 M
  262715. 2090 6806 l
  262716. 1560 7112 l
  262717. 1560 7088 l
  262718. 2070 6206 M
  262719. 2080 6200 l
  262720. 2090 6200 l
  262721. 2090 6806 l
  262722. 2070 6794 l
  262723. 1560 5912 M
  262724. 1560 5888 l
  262725. 2068 6181 l
  262726. 2080 6200 l
  262727. 2070 6206 l
  262728. 1560 5888 M
  262729. 1560 5912 l
  262730. 1050 6206 l
  262731. 1030 6194 l
  262732. 1514 5418 M
  262733. 1534 5418 l
  262734. 1534 5920 l
  262735. 1514 5920 l
  262736. 1586 5418 M
  262737. 1606 5418 l
  262738. 1606 5920 l
  262739. 1586 5920 l
  262740. f[1 4 5686 2859 5963 2555 ]Bd
  262741. 5341 2528 M
  262742. 5441 2462 l
  262743. 5659 2888 l
  262744. 5652 2896 l
  262745. 5636 2892 l
  262746. 2020 5714 M
  262747. 2140 5714 l
  262748. 2090 6200 l
  262749. 2080 6200 l
  262750. 2068 6181 l
  262751. f[1 4 2128 6176 2569 5956 ]Bd
  262752. 3192 6091 M
  262753. 3192 6113 l
  262754. 2614 5942 l
  262755. 2620 5922 l
  262756. 3653 5948 M
  262757. 3659 5968 l
  262758. 3192 6113 l
  262759. 3192 6091 l
  262760. 3085 3365 M
  262761. 3102 3369 l
  262762. 3103 3379 l
  262763. 2638 3554 l
  262764. 2630 3536 l
  262765. 3559 3517 M
  262766. 3553 3535 l
  262767. 3103 3379 l
  262768. 3102 3369 l
  262769. 3109 3361 l
  262770. 2772 3018 M
  262771. 2868 2948 l
  262772. 3109 3361 l
  262773. 3102 3369 l
  262774. 3085 3365 l
  262775. f[1 4 3140 3335 3445 3061 ]Bd
  262776. 4220 3880 2360 3880 2 Ar
  262777. 9720 3840 7980 3840 2 Ar
  262778. count origstk sub{P}rp end
  262779. chemsave restore
  262780.     Helvetica
  262781. Times
  262782.     R= Alkyl
  262783. EWG= CO
  262784. Me, COAc
  262785. \CHMD
  262786. R= Alkyl
  262787. EWG= CO2Me, COAc
  262788.     Helvetica
  262789. Times
  262790. Untitled Document-3
  262791. count
  262792. currentpoint 192837465
  262793. currentpoint
  262794. save/chemsave exch def
  262795. %%BeginProcSet: chemdict30 24 10
  262796. % ChemDraw Laser Prep
  262797. % Copyright 1986-
  262798. 1995, CambridgeSoft Corporation
  262799. userdict/chemdict30 210 dict put
  262800. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L
  262801. /rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d
  262802. /cW 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  262803. x}b/sRmp{cur
  262804. rentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  262805. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  262806. 0 cw 2 dv xl
  262807. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  262808. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  262809. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  262810. St 16 and 0 ne{2 ix 6 m 
  262811. 1 a D ix e D ix e D ix e D ix e P SpA}if
  262812. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  262813. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  262814. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  262815. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  262816. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  262817. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc
  262818.  cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  262819. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  262820. P P}{sq at 2
  262821. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  262822. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  262823. l w .35 dv w
  262824.  -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  262825. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  262826. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  262827. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  262828. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  262829. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 
  262830. -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  262831. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  262832. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  262833. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  262834. 21 -10 27 -8 27 0 cv
  262835. 27 8 21 10 9 6 cv
  262836. -3 2 -3 -2 9 -6 cv
  262837. cp}b/DLB{0 0 M -4.8 4.8 l
  262838. -8 8 -9.6 12 -9.6 16.8 cv
  262839. -9.6 21.6 -8 2
  262840. 4.6 -4.8 25.8 cv
  262841. -1.6 27 1.6 27 4.8 25.8 cv
  262842. 8 24.6 9.6 21.6 9.6 16.8 cv
  262843. 9.6 12 8 8 4.8 4.8 cv
  262844. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  262845. 0 Y X Y rO ac
  262846. X Y X 0 rO ac
  262847. X 0 0 0 rO ac
  262848. 0 0 0 Y rO ac
  262849. cp}b/Rc{0 0 p M
  262850. 0 Y p l
  262851. X Y p l
  262852. X 0 p l
  262853. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  262854. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransfo
  262855. m D 0 lt{n}if sq n D
  262856. CMT dtransform idtransform
  262857. e 2 m e
  262858. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  262859. 32 -0.5 0.5{gs
  262860. 13.5 0 xl
  262861. D 32 s 64 dv 13.5 m D 7 m 24 dv
  262862. -13.5 0 xl
  262863. gr}for
  262864. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  262865. 32 -0.5 0.5{gs
  262866. D 32 s 64 dv 0.65 m D
  262867. gr}for
  262868. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  262869. 32 -0.5 0.5{gs
  262870. D 32 s 64 dv D
  262871. gr}for
  262872. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  262873. 32 -0.5 0.5{gs
  262874. 0 13.5 xl
  262875. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  262876. 0 -13.5 xl
  262877. DLB f
  262878. gr}for
  262879. DLB SM st}{DLB g
  262880. rf}ie}b/gRr{sh{sRmp
  262881. 32 -0.5 0.5{gs
  262882. X 2 dv Y 2 dv xl
  262883. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262884. X -2 dv Y -2 dv xl
  262885. gr}for
  262886. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  262887. 32 -0.5 0.5{gs
  262888. X 2 dv Y 2 dv xl
  262889. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  262890. X -2 dv Y -2 dv xl
  262891. gr}for
  262892. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  262893. rev{1 -1 sc}if
  262894. 0 lW 2 m xl
  262895. D SA OA
  262896. rad 0 xl
  262897. 180 ro
  262898. 0 lW 2 m xl
  262899. SA OA}b/Aos{X Y M SM cpt xl X
  262900. Y e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  262901. o 0 lt o 0 lt ne/rev x
  262902. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  262903. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  262904. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  262905. lp 0 p M
  262906. 0 0 0 Y lp ac
  262907. 0 Y 2 dv lp neg o lp ac
  262908. 0 Y 2 dv 0 Y lp ac
  262909. 0 Y lp Y lp ac
  262910. X lp s 0 p M
  262911. X 0 X Y lp ac
  262912. X Y 2 dv X lp a o lp ac
  262913. X Y 2 dv X Y lp ac
  262914. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 
  262915. pA a arc st
  262916. np X Y s Y 2 dv
  262917. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  262918. rO D rlineto
  262919. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  262920. rO lW -2 dv a Y lW 2 dv a rO a p l
  262921. lW -2 dv Y lW 2 dv a p l
  262922. 0 Y p l X Y p l X 0 p l cp f
  262923. 0 0 p M
  262924. 0 Y p l
  262925. X Y p l
  262926. X 0 p l cp
  262927. SM st}{Rr SM st}{rO Y p M rO rO xl
  262928. 0 Y X Y rO ac
  262929. X Y X 0 rO ac
  262930. X 0 0 0 rO ac
  262931. rO neg D xl X Y 0 Y rO ac
  262932. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  262933. -1 -1 sc LB whf}{Asc gs gLB gr
  262934. -0.4 -0.4 sc LB
  262935.  whf}{Asc LB gs whf gr
  262936. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  262937. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  262938. gs 3.6 12 sc gOv gr
  262939. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  262940. gs 3.6 12 sc Cr whf gr
  262941. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  262942. 0 -1 p M
  262943. 0 0 1 0 1 ac
  262944. 8 0 8 1 1 ac
  262945. 8 0 16 0 1 ac
  262946. 16 0 16 -1 1 ac
  262947. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  262948. 2 dv D sc
  262949. 1 0 M -1 0 l
  262950. 0 1 M 0 -1 l
  262951. Ast}{XY 
  262952. D X Y dt 0 0 M SM cpt xl
  262953. 2 dv D sc
  262954. 1 0 M -1 0 l
  262955. Ast}{4.5 Aos
  262956. 1 0 M -1 0 l
  262957. 0 1 M 0 -1 l
  262958. 2 0 M 0 0 2 0 360 arc
  262959. Ast}{4.5 Aos
  262960. 1 0 M -1 0 l
  262961. 2 0 M 0 0 2 0 360 arc
  262962. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  262963. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  262964. 1 -1 M -1 -1 l
  262965. 0 2 M 0 -2 l
  262966. Ast}{5 Aos
  262967. 1 -1 M -1 -1 l
  262968. 1 1 M -1 1 l
  262969. 0 2 M 0 -2 l
  262970. Ast}{4.5 Aos
  262971. 1 0 M -1 0 l
  262972. 0 1 M 0 -1 l
  262973. Ast}{4.5 Aos
  262974. 1 0 M -1 0 l
  262975. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB g
  262976. s whf gr
  262977. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  262978. gs 3.6 12 sc Cr whf gr
  262979. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  262980. gs 3.6 12 sc Cr blf gr
  262981. ZLB whf}{Asc LB gs whf gr
  262982. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  262983. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  262984. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  262985. e 2 ix a}b/PT{D 
  262986. 2 4 gi al P OP D 1 sc
  262987. o length 6 gt{P 6 g}{e P 8 dv}ie
  262988. D lW 2 m lt{P lW 2 m}if
  262989. 0 e p
  262990. 0 0 p
  262991. 3 -1 r s 3 1 r e s e
  262992. 0 0 p M 1 0 p l
  262993. 0 0 p ap M 1 0 p ap l
  262994. e n e n
  262995. 0 0 p ap M 1 0 p ap l
  262996. P P}b/DT{gs np PT SM st gr}b
  262997. O/NH{lW s D hS dv ru
  262998. cvi D 0 eq{P 1}if/nH x
  262999. D hS nH m s
  263000. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  263001. bW 2 dv/bd x
  263002. lW 2 dv e D NH e{D bd p M bd n p l}for
  263003. st gr}{gs 12 OB np
  263004. lW 2 dv 0 xl NH 1 sc
  263005. bW 2 dv wF m nH 1
  263006.  a dv/bd x
  263007. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  263008. np 0 lW 2 dv o o n p M p l bW 2 dv
  263009. wF m o o p l n p l
  263010. cp f gr}{P}{gs 12 OB/bL x
  263011. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  263012. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  263013. bL nSq 2 m dv D sc
  263014. nSq{.135  .667 .865  .667 1 0 rcurveto
  263015. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  263016. np 0 lW 2 dv o o n p M p l bW 2 dv
  263017. wF m o o p l n p l
  263018. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  263019. 1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  263020. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  263021. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  263022. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  263023. 5 -1 r dv neg e 5 -1 r dv neg e
  263024. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  263025. %%EndProcSet
  263026. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  263027. 600 232 36 106 SPn/origstk x
  263028. 65535 65535 65535 sBg
  263029. 0 0 0 C
  263030. 1060 3174 M
  263031. 1040 3186 l
  263032. 1040 2574 l
  263033. 1060 2586 l
  263034. 1132 3138 M
  263035. 1112 3138 l
  263036. 1112 2622 l
  263037. 1132 2622 l
  263038. 1570 3468 M
  263039. 1570 3492 l
  263040. 0 3186 l
  263041. 1060 3174 l
  263042. 2080 3174 M
  263043. 2100 3186 l
  263044. 1570 3492 l
  263045. 1570 3468 l
  263046. 2013 3129 M
  263047. 2023 3147 l
  263048. 1575 3406 l
  263049. 1565 3388 l
  263050. 2080 2586 M
  263051. 2090 2580 l
  263052. 2100 2586 l
  263053. 2100 3186 l
  263054. 2080 3174 l
  263055. 1570 2292 M
  263056. 1570 2268 l
  263057. 2090 2568 l
  263058. 2090 2580 l
  263059. 2080 2586 l
  263060. 1565 2372 M
  263061. 1575 2354 l
  263062. 2023 2613 l
  263063. 2013 2631 l
  263064. 1570 2268 M
  263065. 1570 2292 l
  263066. 1060 2586 l
  263067. 1040 2574 l
  263068. 2610 2268 M
  263069. 2610 2292 l
  263070. 2100 2586 l
  263071. 2090 2580 l
  263072. 2090 2568 l
  263073. 3130 2568 M
  263074. 3130 2592 l
  263075. 2610 2292 l
  263076. 610 2268 l
  263077. 3135 2488 M
  263078. 3125 2506 l
  263079. 2641 2227 l
  263080. 2651 2209 l
  263081. 3649 2268 M
  263082. 3649 2292 l
  263083. 3130 2592 l
  263084. 3130 2568 l
  263085. 4174 2571 M
  263086. 4164 2589 l
  263087. 3649 2292 l
  263088. 3649 2268 l
  263089. 4138 2633 M
  263090. 4128 2651 l
  263091. 3644 2372 l
  263092. 3654 2354 l
  263093. 6550 2760 4390 2760 2 Ar
  263094. 7810 2628 M
  263095. 7810 2652 l
  263096. 7368 2907 l
  263097. 7358 2889 l
  263098. 8330 2928 M
  263099. 8330 2952 l
  263100. 7810 2652 l
  263101. 7810 2628 l
  263102. 8335 2848 M
  263103. 8325 2866 l
  263104. 7841 2587 l
  263105. 7851 2569 l
  263106. 8850 2628 M
  263107. 8850 2652 l
  263108. 8330 2952 l
  263109. 8330 2928 l
  263110. 375 2931 M
  263111. 9365 2949 l
  263112. 8850 2652 l
  263113. 8850 2628 l
  263114. 11060 2578 M
  263115. 11060 2602 l
  263116. 10622 2855 l
  263117. 10612 2837 l
  263118. 11580 2878 M
  263119. 11580 2902 l
  263120. 11060 2602 l
  263121. 11060 2578 l
  263122. 12100 2578 M
  263123. 12100 2602 l
  263124. 11580 2902 l
  263125. 11580 2878 l
  263126. 12625 2881 M
  263127. 12615 2899 l
  263128. 12100 2602 l
  263129. 12100 2578 l
  263130. 930 4794 M
  263131. 910 4806 l
  263132. 910 4194 l
  263133. 930 4206 l
  263134. 1002 4758 M
  263135. 982 4758 l
  263136. 982 4242 l
  263137. 1002 4242 l
  263138. 1440 5088 M
  263139. 1440 5112 l
  263140. 910 4806 l
  263141. 930 4794 l
  263142. 1950 4794 M
  263143. 1970 4806 l
  263144. 1440 5112 l
  263145. 0 5088 l
  263146. 1950 4206 M
  263147. 1960 4200 l
  263148. 1970 4206 l
  263149. 1970 4806 l
  263150. 1950 4794 l
  263151. 1440 3912 M
  263152. 1440 3888 l
  263153. 1960 4188 l
  263154. 1960 4200 l
  263155. 1950 4206 l
  263156. 1435 3992 M
  263157. 1445 3974 l
  263158. 1893 4233 l
  263159. 1883 4251 l
  263160. 1440 3888 M
  263161. 1440 3912 l
  263162. 930 4206 l
  263163. 910 4194 l
  263164. 2371 3951 M
  263165. 2381 3969 l
  263166. 1970 4206 l
  263167. 1960 4200 l
  263168. 1960 4188 l
  263169. 5620 4120 3880 4120 2 Ar
  263170. 6730 4754 M
  263171. 6710 4766 l
  263172. 6710 4154 l
  263173. 6730 4166 l
  263174. 7240 5048 M
  263175. 7240 5072 l
  263176. 6710 4766 l
  263177. 6730 4754 l
  263178. 7750 4754 M
  263179. 7770 4766 l
  263180. 240 5072 l
  263181. 7240 5048 l
  263182. 7750 4166 M
  263183. 7760 4160 l
  263184. 7770 4166 l
  263185. 7770 4766 l
  263186. 7750 4754 l
  263187. 7240 3872 M
  263188. 7240 3848 l
  263189. 7760 4148 l
  263190. 7760 4160 l
  263191. 7750 4166 l
  263192. 7235 3952 M
  263193. 7245 3934 l
  263194. 7693 4193 l
  263195. 7683 4211 l
  263196. 7240 3848 M
  263197. 7240 3872 l
  263198. 6730 4166 l
  263199. 6710 4154 l
  263200. 8171 3911 M
  263201. 8181 3929 l
  263202. 7770 4166 l
  263203. 7760 4160 l
  263204. 7760 4148 l
  263205. 810 6364 M
  263206. 790 6376 l
  263207. 790 5764 l
  263208. 810 5776 l
  263209. 882 6328 M
  263210. 862 6328 l
  263211. 862 5812 l
  263212. 882 5812 l
  263213. 1320 6658 M
  263214. 1320 6682 l
  263215. 790 6376 l
  263216. 810 6364
  263217. 1830 6364 M
  263218. 1850 6376 l
  263219. 1320 6682 l
  263220. 1320 6658 l
  263221. 1830 5776 M
  263222. 1840 5770 l
  263223. 1850 5776 l
  263224. 1850 6376 l
  263225. 1830 6364 l
  263226. 1320 5482 M
  263227. 1320 5458 l
  263228. 1840 5758 l
  263229. 1840 5770 l
  263230. 1830 5776 l
  263231. 1315 5562 M
  263232. 1325 5544 l
  263233. 1773 5803 l
  263234. 1763 5821 l
  263235. 1320 5458 M
  263236. 1320 5482 l
  263237. 810 5776 l
  263238. 790 5764 l
  263239. 2229 5533 M
  263240. 2239 5551 l
  263241. 1850 5776 l
  263242. 1840 5770 l
  263243. 1840 5758 l
  263244. 5500 5690 3760 5690 2 Ar
  263245. 6610 6324 M
  263246. 6590 6336 l
  263247. 6590 5724 l
  263248. 6610 5736 l
  263249. 7120 6618 M
  263250. 7120 6642 l
  263251. 6590 63
  263252. 6610 6324 l
  263253. 7630 6324 M
  263254. 7650 6336 l
  263255. 7120 6642 l
  263256. 7120 6618 l
  263257. 7630 5736 M
  263258. 7640 5730 l
  263259. 7650 5736 l
  263260. 7650 6336 l
  263261. 7630 6324 l
  263262. 7120 5442 M
  263263. 7120 5418 l
  263264. 7640 5718 l
  263265. 7640 5730 l
  263266. 7630 5736 l
  263267. 7115 5522 M
  263268. 7125 5504 l
  263269. 7573 5763 l
  263270. 7563 5781 l
  263271. 7120 5418 M
  263272. 7120 5442 l
  263273. 6610 5736 l
  263274. 6590 5724 l
  263275. 8029 5493 M
  263276. 8039 5511 l
  263277. 7650 5736 l
  263278. 7640 5730 l
  263279. 7640 5718 l
  263280. count origstk sub{P}rp end
  263281. chemsave restore
  263282. Times
  263283. [(t-Bu
  263284. PH)PdP(t-Bu)
  263285.  (1atm)
  263286.     Helvetica
  263287. 2CHMD
  263288. Bu2PH)PdP(t-Bu)2]2
  263289. H2 (1atm)
  263290.     Helvetica
  263291. Times
  263292. NswsD
  263293.     Helvetica
  263294. [(t-Bu2PH)PdP(t-Bu)2]2
  263295. H2 (1atm)
  263296.     Helvetica
  263297.     Helvetica
  263298.     Helvetica
  263299. COMe<
  263300. COMe6
  263301.     Helvetica
  263302. COMe<
  263303. COMe6
  263304.     Helvetica
  263305.     Helvetica
  263306. Untitled Document-2
  263307. count
  263308. currentpoint 192837465
  263309. currentpoint
  263310. save/chemsave exch def
  263311. %%BeginProcSet: chemdict30 24 10
  263312. % ChemDraw Laser Prep
  263313. % Copyright 1986-
  263314. 1995, CambridgeSoft Corporation
  263315. userdict/chemdict30 210 dict put
  263316. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L
  263317. /rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d
  263318. /cW 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  263319. x}b/sRmp{cur
  263320. rentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  263321. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  263322. 0 cw 2 dv xl
  263323. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  263324. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  263325. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  263326. St 16 and 0 ne{2 ix 6 m 
  263327. 1 a D ix e D ix e D ix e D ix e P SpA}if
  263328. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  263329. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  263330. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  263331. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  263332. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  263333. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc
  263334.  cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  263335. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  263336. P P}{sq at 2
  263337. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  263338. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  263339. l w .35 dv w
  263340.  -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  263341. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  263342. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  263343. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  263344. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  263345. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 
  263346. -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  263347. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  263348. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  263349. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  263350. 21 -10 27 -8 27 0 cv
  263351. 27 8 21 10 9 6 cv
  263352. -3 2 -3 -2 9 -6 cv
  263353. cp}b/DLB{0 0 M -4.8 4.8 l
  263354. -8 8 -9.6 12 -9.6 16.8 cv
  263355. -9.6 21.6 -8 2
  263356. 4.6 -4.8 25.8 cv
  263357. -1.6 27 1.6 27 4.8 25.8 cv
  263358. 8 24.6 9.6 21.6 9.6 16.8 cv
  263359. 9.6 12 8 8 4.8 4.8 cv
  263360. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  263361. 0 Y X Y rO ac
  263362. X Y X 0 rO ac
  263363. X 0 0 0 rO ac
  263364. 0 0 0 Y rO ac
  263365. cp}b/Rc{0 0 p M
  263366. 0 Y p l
  263367. X Y p l
  263368. X 0 p l
  263369. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  263370. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransfo
  263371. m D 0 lt{n}if sq n D
  263372. CMT dtransform idtransform
  263373. e 2 m e
  263374. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  263375. 32 -0.5 0.5{gs
  263376. 13.5 0 xl
  263377. D 32 s 64 dv 13.5 m D 7 m 24 dv
  263378. -13.5 0 xl
  263379. gr}for
  263380. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  263381. 32 -0.5 0.5{gs
  263382. D 32 s 64 dv 0.65 m D
  263383. gr}for
  263384. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  263385. 32 -0.5 0.5{gs
  263386. D 32 s 64 dv D
  263387. gr}for
  263388. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  263389. 32 -0.5 0.5{gs
  263390. 0 13.5 xl
  263391. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  263392. 0 -13.5 xl
  263393. DLB f
  263394. gr}for
  263395. DLB SM st}{DLB g
  263396. rf}ie}b/gRr{sh{sRmp
  263397. 32 -0.5 0.5{gs
  263398. X 2 dv Y 2 dv xl
  263399. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  263400. X -2 dv Y -2 dv xl
  263401. gr}for
  263402. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  263403. 32 -0.5 0.5{gs
  263404. X 2 dv Y 2 dv xl
  263405. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  263406. X -2 dv Y -2 dv xl
  263407. gr}for
  263408. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  263409. rev{1 -1 sc}if
  263410. 0 lW 2 m xl
  263411. D SA OA
  263412. rad 0 xl
  263413. 180 ro
  263414. 0 lW 2 m xl
  263415. SA OA}b/Aos{X Y M SM cpt xl X
  263416. Y e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  263417. o 0 lt o 0 lt ne/rev x
  263418. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  263419. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  263420. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  263421. lp 0 p M
  263422. 0 0 0 Y lp ac
  263423. 0 Y 2 dv lp neg o lp ac
  263424. 0 Y 2 dv 0 Y lp ac
  263425. 0 Y lp Y lp ac
  263426. X lp s 0 p M
  263427. X 0 X Y lp ac
  263428. X Y 2 dv X lp a o lp ac
  263429. X Y 2 dv X Y lp ac
  263430. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 
  263431. pA a arc st
  263432. np X Y s Y 2 dv
  263433. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  263434. rO D rlineto
  263435. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  263436. rO lW -2 dv a Y lW 2 dv a rO a p l
  263437. lW -2 dv Y lW 2 dv a p l
  263438. 0 Y p l X Y p l X 0 p l cp f
  263439. 0 0 p M
  263440. 0 Y p l
  263441. X Y p l
  263442. X 0 p l cp
  263443. SM st}{Rr SM st}{rO Y p M rO rO xl
  263444. 0 Y X Y rO ac
  263445. X Y X 0 rO ac
  263446. X 0 0 0 rO ac
  263447. rO neg D xl X Y 0 Y rO ac
  263448. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  263449. -1 -1 sc LB whf}{Asc gs gLB gr
  263450. -0.4 -0.4 sc LB
  263451.  whf}{Asc LB gs whf gr
  263452. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  263453. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  263454. gs 3.6 12 sc gOv gr
  263455. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  263456. gs 3.6 12 sc Cr whf gr
  263457. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  263458. 0 -1 p M
  263459. 0 0 1 0 1 ac
  263460. 8 0 8 1 1 ac
  263461. 8 0 16 0 1 ac
  263462. 16 0 16 -1 1 ac
  263463. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  263464. 2 dv D sc
  263465. 1 0 M -1 0 l
  263466. 0 1 M 0 -1 l
  263467. Ast}{XY 
  263468. D X Y dt 0 0 M SM cpt xl
  263469. 2 dv D sc
  263470. 1 0 M -1 0 l
  263471. Ast}{4.5 Aos
  263472. 1 0 M -1 0 l
  263473. 0 1 M 0 -1 l
  263474. 2 0 M 0 0 2 0 360 arc
  263475. Ast}{4.5 Aos
  263476. 1 0 M -1 0 l
  263477. 2 0 M 0 0 2 0 360 arc
  263478. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  263479. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  263480. 1 -1 M -1 -1 l
  263481. 0 2 M 0 -2 l
  263482. Ast}{5 Aos
  263483. 1 -1 M -1 -1 l
  263484. 1 1 M -1 1 l
  263485. 0 2 M 0 -2 l
  263486. Ast}{4.5 Aos
  263487. 1 0 M -1 0 l
  263488. 0 1 M 0 -1 l
  263489. Ast}{4.5 Aos
  263490. 1 0 M -1 0 l
  263491. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB g
  263492. s whf gr
  263493. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  263494. gs 3.6 12 sc Cr whf gr
  263495. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  263496. gs 3.6 12 sc Cr blf gr
  263497. ZLB whf}{Asc LB gs whf gr
  263498. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  263499. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  263500. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  263501. e 2 ix a}b/PT{D 
  263502. 2 4 gi al P OP D 1 sc
  263503. o length 6 gt{P 6 g}{e P 8 dv}ie
  263504. D lW 2 m lt{P lW 2 m}if
  263505. 0 e p
  263506. 0 0 p
  263507. 3 -1 r s 3 1 r e s e
  263508. 0 0 p M 1 0 p l
  263509. 0 0 p ap M 1 0 p ap l
  263510. e n e n
  263511. 0 0 p ap M 1 0 p ap l
  263512. P P}b/DT{gs np PT SM st gr}b
  263513. O/NH{lW s D hS dv ru
  263514. cvi D 0 eq{P 1}if/nH x
  263515. D hS nH m s
  263516. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  263517. bW 2 dv/bd x
  263518. lW 2 dv e D NH e{D bd p M bd n p l}for
  263519. st gr}{gs 12 OB np
  263520. lW 2 dv 0 xl NH 1 sc
  263521. bW 2 dv wF m nH 1
  263522.  a dv/bd x
  263523. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  263524. np 0 lW 2 dv o o n p M p l bW 2 dv
  263525. wF m o o p l n p l
  263526. cp f gr}{P}{gs 12 OB/bL x
  263527. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  263528. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  263529. bL nSq 2 m dv D sc
  263530. nSq{.135  .667 .865  .667 1 0 rcurveto
  263531. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  263532. np 0 lW 2 dv o o n p M p l bW 2 dv
  263533. wF m o o p l n p l
  263534. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  263535. 1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  263536. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  263537. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  263538. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  263539. 5 -1 r dv neg e 5 -1 r dv neg e
  263540. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  263541. %%EndProcSet
  263542. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  263543. 533 97 44 134 SPn/origstk x
  263544. 65535 65535 65535 sBg
  263545. 0 0 0 C
  263546. 1500 3864 M
  263547. 1490 3870 l
  263548. 1480 3864 l
  263549. 1480 3270 l
  263550. 1500 3270 l
  263551. 2590 3270 2040 3270 36 Ar
  263552. 2577 3818 M
  263553. 2557 3818 l
  263554. 2580 3230 l
  263555. 2600 3230 l
  263556. 1075 41
  263557. 1065 4104 l
  263558. 1480 3864 l
  263559. 1490 3870 l
  263560. 1490 3882 l
  263561. 1907 4099 M
  263562. 1897 4117 l
  263563. 1490 3882 l
  263564. 1490 3870 l
  263565. 1500 3864 l
  263566. 2322 4367 M
  263567. 2304 4359 l
  263568. 2558 3814 l
  263569. 2576 3822 l
  263570. 3183 3939 M
  263571. 3177 3959 l
  263572. 2565 3790 l
  263573. 2571 3770 l
  263574. 3163 4011 M
  263575. 3157 4031 l
  263576. 2548 3862 l
  263577. 2554 3842 l
  263578. 8280 3914 M
  263579. 8270 3920 l
  263580. 8260 3914 l
  263581. 8260 3320 l
  263582. 8280 3320 l
  263583. 9370 3320 8820 3320 36 Ar
  263584. 7855 4172 M
  263585. 7845 4154 l
  263586. 8260 3914 l
  263587. 8270 3920 l
  263588. 8270 3932 l
  263589. 8695 4154 M
  263590. 8685 4172 l
  263591. 8270 3932 
  263592. 8270 3920 l
  263593. 8280 3914 l
  263594. 9380 3914 M
  263595. 9370 3920 l
  263596. 9360 3914 l
  263597. 9360 3320 l
  263598. 9380 3320 l
  263599. 8915 4168 M
  263600. 8905 4150 l
  263601. 9360 3914 l
  263602. 9370 3920 l
  263603. 9359 3937 l
  263604. 9883 4220 M
  263605. 9883 4244 l
  263606. 9379 3938 l
  263607. 9370 3920 l
  263608. 9380 3914 l
  263609. 9359 4520 M
  263610. 9339 4520 l
  263611. 9359 3937 l
  263612. 9370 3920 l
  263613. 9379 3938 l
  263614. 10409 3932 M
  263615. 10409 3956 l
  263616. 9883 4244 l
  263617. 9883 4220 l
  263618. 10921 4243 M
  263619. 10921 4267 l
  263620. 10409 3956 l
  263621. 10409 3932 l
  263622. 10928 4163 M
  263623. 10918 4181 l
  263624. 10441 3892 l
  263625. 10451 3874 l
  263626. 11345 4011
  263627. 11355 4029 l
  263628. 10921 4267 l
  263629. 10921 4243 l
  263630. 7150 3770 3870 3770 2 Ar
  263631. 4930 3918 M
  263632. 4930 3942 l
  263633. 4415 4239 l
  263634. 4405 4221 l
  263635. 4889 3859 M
  263636. 4899 3877 l
  263637. 4379 4177 l
  263638. 4369 4159 l
  263639. 5355 4164 M
  263640. 5345 4182 l
  263641. 4930 3942 l
  263642. 4930 3918 l
  263643. count origstk sub{P}rp end
  263644. chemsave restore
  263645.     Helvetica
  263646. Times
  263647. Pd(OAc)
  263648. (0.1 mol-eq)
  263649. CuCl   (1 mol-eq),  O
  263650. , DMF
  263651. %    5  mol-eq
  263652. 3Pd(OAc)2   (0.1 mol-eq)
  263653. CuCl   (1 mol-eq),  O2, DMF
  263654.     5  mol-eq(
  263655.     Helvetica
  263656. Times
  263657.     Helvetica
  263658.     Helvetica
  263659.     Helvetica
  263660.     Helvetica
  263661.     Helvetica
  263662.     Helvetica
  263663. 3Pd(OAc)2   (0.1 mol-eq)
  263664. CuCl   (1 mol-eq),  O2, DMF
  263665.     Helvetica
  263666.     5  mol-eq
  263667. Untitled Refs-3
  263668. count
  263669. currentpoint 192837465
  263670. currentpoint
  263671. save/chemsave exch def
  263672. %%BeginProcSet: chemdict30 24 10
  263673. % ChemDraw Laser Prep
  263674. % Copyright 1986-1995
  263675. 1995, CambridgeSoft Corporation
  263676. userdict/chemdict30 210 dict put
  263677. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L
  263678. /rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d
  263679. /cW 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  263680. x}b/sRmp{cur
  263681. rentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  263682. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  263683. 0 cw 2 dv xl
  263684. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  263685. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  263686. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  263687. St 16 and 0 ne{2 ix 6 m 
  263688. 1 a D ix e D ix e D ix e D ix e P SpA}if
  263689. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  263690. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  263691. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  263692. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  263693. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  263694. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc
  263695.  cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  263696. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  263697. P P}{sq at 2
  263698. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  263699. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  263700. l w .35 dv w
  263701.  -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  263702. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  263703. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  263704. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  263705. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  263706. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 
  263707. -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  263708. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  263709. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  263710. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  263711. 21 -10 27 -8 27 0 cv
  263712. 27 8 21 10 9 6 cv
  263713. -3 2 -3 -2 9 -6 cv
  263714. cp}b/DLB{0 0 M -4.8 4.8 l
  263715. -8 8 -9.6 12 -9.6 16.8 cv
  263716. -9.6 21.6 -8 2
  263717. 4.6 -4.8 25.8 cv
  263718. -1.6 27 1.6 27 4.8 25.8 cv
  263719. 8 24.6 9.6 21.6 9.6 16.8 cv
  263720. 9.6 12 8 8 4.8 4.8 cv
  263721. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  263722. 0 Y X Y rO ac
  263723. X Y X 0 rO ac
  263724. X 0 0 0 rO ac
  263725. 0 0 0 Y rO ac
  263726. cp}b/Rc{0 0 p M
  263727. 0 Y p l
  263728. X Y p l
  263729. X 0 p l
  263730. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  263731. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransfo
  263732. m D 0 lt{n}if sq n D
  263733. CMT dtransform idtransform
  263734. e 2 m e
  263735. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  263736. 32 -0.5 0.5{gs
  263737. 13.5 0 xl
  263738. D 32 s 64 dv 13.5 m D 7 m 24 dv
  263739. -13.5 0 xl
  263740. gr}for
  263741. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  263742. 32 -0.5 0.5{gs
  263743. D 32 s 64 dv 0.65 m D
  263744. gr}for
  263745. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  263746. 32 -0.5 0.5{gs
  263747. D 32 s 64 dv D
  263748. gr}for
  263749. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  263750. 32 -0.5 0.5{gs
  263751. 0 13.5 xl
  263752. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  263753. 0 -13.5 xl
  263754. DLB f
  263755. gr}for
  263756. DLB SM st}{DLB g
  263757. rf}ie}b/gRr{sh{sRmp
  263758. 32 -0.5 0.5{gs
  263759. X 2 dv Y 2 dv xl
  263760. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  263761. X -2 dv Y -2 dv xl
  263762. gr}for
  263763. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  263764. 32 -0.5 0.5{gs
  263765. X 2 dv Y 2 dv xl
  263766. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  263767. X -2 dv Y -2 dv xl
  263768. gr}for
  263769. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  263770. rev{1 -1 sc}if
  263771. 0 lW 2 m xl
  263772. D SA OA
  263773. rad 0 xl
  263774. 180 ro
  263775. 0 lW 2 m xl
  263776. SA OA}b/Aos{X Y M SM cpt xl X
  263777. Y e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  263778. o 0 lt o 0 lt ne/rev x
  263779. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  263780. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  263781. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  263782. lp 0 p M
  263783. 0 0 0 Y lp ac
  263784. 0 Y 2 dv lp neg o lp ac
  263785. 0 Y 2 dv 0 Y lp ac
  263786. 0 Y lp Y lp ac
  263787. X lp s 0 p M
  263788. X 0 X Y lp ac
  263789. X Y 2 dv X lp a o lp ac
  263790. X Y 2 dv X Y lp ac
  263791. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 
  263792. pA a arc st
  263793. np X Y s Y 2 dv
  263794. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  263795. rO D rlineto
  263796. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  263797. rO lW -2 dv a Y lW 2 dv a rO a p l
  263798. lW -2 dv Y lW 2 dv a p l
  263799. 0 Y p l X Y p l X 0 p l cp f
  263800. 0 0 p M
  263801. 0 Y p l
  263802. X Y p l
  263803. X 0 p l cp
  263804. SM st}{Rr SM st}{rO Y p M rO rO xl
  263805. 0 Y X Y rO ac
  263806. X Y X 0 rO ac
  263807. X 0 0 0 rO ac
  263808. rO neg D xl X Y 0 Y rO ac
  263809. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  263810. -1 -1 sc LB whf}{Asc gs gLB gr
  263811. -0.4 -0.4 sc LB
  263812.  whf}{Asc LB gs whf gr
  263813. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  263814. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  263815. gs 3.6 12 sc gOv gr
  263816. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  263817. gs 3.6 12 sc Cr whf gr
  263818. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  263819. 0 -1 p M
  263820. 0 0 1 0 1 ac
  263821. 8 0 8 1 1 ac
  263822. 8 0 16 0 1 ac
  263823. 16 0 16 -1 1 ac
  263824. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  263825. 2 dv D sc
  263826. 1 0 M -1 0 l
  263827. 0 1 M 0 -1 l
  263828. Ast}{XY 
  263829. D X Y dt 0 0 M SM cpt xl
  263830. 2 dv D sc
  263831. 1 0 M -1 0 l
  263832. Ast}{4.5 Aos
  263833. 1 0 M -1 0 l
  263834. 0 1 M 0 -1 l
  263835. 2 0 M 0 0 2 0 360 arc
  263836. Ast}{4.5 Aos
  263837. 1 0 M -1 0 l
  263838. 2 0 M 0 0 2 0 360 arc
  263839. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  263840. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  263841. 1 -1 M -1 -1 l
  263842. 0 2 M 0 -2 l
  263843. Ast}{5 Aos
  263844. 1 -1 M -1 -1 l
  263845. 1 1 M -1 1 l
  263846. 0 2 M 0 -2 l
  263847. Ast}{4.5 Aos
  263848. 1 0 M -1 0 l
  263849. 0 1 M 0 -1 l
  263850. Ast}{4.5 Aos
  263851. 1 0 M -1 0 l
  263852. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB g
  263853. s whf gr
  263854. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  263855. gs 3.6 12 sc Cr whf gr
  263856. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  263857. gs 3.6 12 sc Cr blf gr
  263858. ZLB whf}{Asc LB gs whf gr
  263859. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  263860. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  263861. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  263862. e 2 ix a}b/PT{D 
  263863. 2 4 gi al P OP D 1 sc
  263864. o length 6 gt{P 6 g}{e P 8 dv}ie
  263865. D lW 2 m lt{P lW 2 m}if
  263866. 0 e p
  263867. 0 0 p
  263868. 3 -1 r s 3 1 r e s e
  263869. 0 0 p M 1 0 p l
  263870. 0 0 p ap M 1 0 p ap l
  263871. e n e n
  263872. 0 0 p ap M 1 0 p ap l
  263873. P P}b/DT{gs np PT SM st gr}b
  263874. O/NH{lW s D hS dv ru
  263875. cvi D 0 eq{P 1}if/nH x
  263876. D hS nH m s
  263877. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  263878. bW 2 dv/bd x
  263879. lW 2 dv e D NH e{D bd p M bd n p l}for
  263880. st gr}{gs 12 OB np
  263881. lW 2 dv 0 xl NH 1 sc
  263882. bW 2 dv wF m nH 1
  263883.  a dv/bd x
  263884. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  263885. np 0 lW 2 dv o o n p M p l bW 2 dv
  263886. wF m o o p l n p l
  263887. cp f gr}{P}{gs 12 OB/bL x
  263888. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  263889. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  263890. bL nSq 2 m dv D sc
  263891. nSq{.135  .667 .865  .667 1 0 rcurveto
  263892. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  263893. np 0 lW 2 dv o o n p M p l bW 2 dv
  263894. wF m o o p l n p l
  263895. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  263896. 1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  263897. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  263898. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  263899. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  263900. 5 -1 r dv neg e 5 -1 r dv neg e
  263901. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  263902. %%EndProcSet
  263903. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW 
  263904. x/bW x/cW x/sh T d
  263905. 520 147 19 62 SPn/origstk x
  263906. 65535 65535 65535 sBg
  263907. 0 0 0 C
  263908. 990 2516 M
  263909. 970 2504 l
  263910. 970 1904 l
  263911. 990 1916 l
  263912. 2010 1916 M
  263913. 2020 1910 l
  263914. 2030 1916 l
  263915. 2030 2510 l
  263916. 2010 2510 l
  263917. 1500 1622 M
  263918. 1500 1598 l
  263919. 2008 1891 l
  263920. 2020 1910 l
  263921. 2010 1916 l
  263922. 1500 1598 M
  263923. 1500 1622 l
  263924. 990 1916 l
  263925. 970 1904 l
  263926. 3050 1916 M
  263927. 3070 1904 l
  263928. 3070 2504 l
  263929. 3050 2516 l
  263930. 2645 1682 M
  263931. 2655 1664 l
  263932. 3070 1904 l
  263933. 3050 1916 l
  263934. 2425 1664 M
  263935. 2435 1682 l
  263936. 2030 1916 l
  263937. 2020 1910 l
  263938. 2032 1891 l
  263939. 3570 2816 M
  263940. 3590 2804 l
  263941. 3590 3410 l
  263942. 3570 3410 l
  263943. 3590 2804 M
  263944. 3570 2816 l
  263945. 3050 2516 l
  263946. 3070 2504 l
  263947. 3621 2739 M
  263948. 3611 2757 l
  263949. 3127 2477 l
  263950. 3137 2459 l
  263951. 470 2816 M
  263952. 450 2804 l
  263953. 970 2504 l
  263954. 990 2516 l
  263955. 470 3410 M
  263956. 450 3410 l
  263957. 450 2804 l
  263958. 470 2816 l
  263959. 542 3410 M
  263960. 522 3410 l
  263961. 522 2852 l
  263962. 542 2852 l
  263963. 2010 2510 M
  263964. 2030 2510 l
  263965. 2030 3110 l
  263966. 2010 3110 l
  263967. 2082 2510 M
  263968. 2102 2510 l
  263969. 2102 3110 l
  263970. 2082 3110 l
  263971. 1938 2510 M
  263972. 1958 2510 l
  263973. 1958 3110 l
  263974. 1938 3110 l
  263975. 2030 3710 M
  263976. 2010 3710 l
  263977. 2010 3110 l
  263978. 2030 3110 l
  263979. 1960 1310 M
  263980. 2080 1310 l
  263981. 2032 1891 l
  263982. 2020 1910 l
  263983. 2008 1891 l
  263984. 7280 2530 5340 2530 2 Ar
  263985. 8610 2504 M
  263986. 8590 2516 l
  263987. 8590 1904 l
  263988. 8610 1916 l
  263989. 9120 2798 M
  263990. 9120 2822 l
  263991. 8590 2516 l
  263992. 8610 2504 l
  263993. 9630 2504 M
  263994. 9640 2510 l
  263995. 9640 2522 l
  263996. 9120 2822 l
  263997. 9120 2798 l
  263998. 9563 2459 M
  263999. 9573 2477 l
  264000. 9125 2736 l
  264001. 9115 2718 l
  264002. 9630 1916 M
  264003. 9640 1910 l
  264004. 9650 1916 l
  264005. 9650 2504 l
  264006. 9640 2510 l
  264007. 9630 2504 l
  264008. 9120 1622 M
  264009. 9120 1598 
  264010. 9628 1891 l
  264011. 9640 1910 l
  264012. 9630 1916 l
  264013. 9120 1598 M
  264014. 9120 1622 l
  264015. 8610 1916 l
  264016. 8590 1904 l
  264017. 10160 2798 M
  264018. 10160 2810 l
  264019. 10150 2816 l
  264020. 9640 2522 l
  264021. 9640 2510 l
  264022. 9650 2504 l
  264023. 10670 2504 M
  264024. 10690 2516 l
  264025. 10170 2816 l
  264026. 10160 2810 l
  264027. 10160 2798 l
  264028. 10603 2459 M
  264029. 10613 2477 l
  264030. 10165 2736 l
  264031. 10155 2718 l
  264032. 10670 1916 M
  264033. 10690 1904 l
  264034. 10690 2516 l
  264035. 10670 2504 l
  264036. 10265 1682 M
  264037. 10275 1664 l
  264038. 10690 1904 l
  264039. 10670 1916 l
  264040. 10045 1664 M
  264041. 10055 1682 l
  264042. 9650 1916 l
  264043. 9640 1910 l
  264044. 9652 1
  264045. 891 l
  264046. 10170 3410 M
  264047. 10150 3410 l
  264048. 10150 2816 l
  264049. 10160 2810 l
  264050. 10170 2816 l
  264051. 9580 1310 M
  264052. 9700 1310 l
  264053. 9652 1891 l
  264054. 9640 1910 l
  264055. 9628 1891 l
  264056. 6162 3538 M
  264057. 6174 3558 l
  264058. 5820 3558 l
  264059. 5820 3538 l
  264060. 6136 3482 M
  264061. 6136 3502 l
  264062. 5820 3502 l
  264063. 5820 3482 l
  264064. 6396 3132 M
  264065. 6408 3152 l
  264066. 6174 3558 l
  264067. 6162 3538 l
  264068. 6864 3132 M
  264069. 6870 3142 l
  264070. 6864 3152 l
  264071. 6408 3152 l
  264072. 6396 3132 l
  264073. 6838 3188 M
  264074. 6838 3208 l
  264075. 6434 3208 l
  264076. 6434 3188 l
  264077. 7028 2850 M
  264078. 7046 2860 l
  264079. 6882 3142 l
  264080. 6870 3142 l
  264081. 6864 3132 l
  264082. 7043 3422 M
  264083. 7025 3432 l
  264084. 6864 3152 l
  264085. 6870 3142 l
  264086. 6882 3142 l
  264087. 5710 3900 M
  264088. 5690 3900 l
  264089. 5690 3660 l
  264090. 5710 3660 l
  264091. 5690 3200 M
  264092. 5710 3200 l
  264093. 5710 3420 l
  264094. 5690 3420 l
  264095. f[1 4 5529 3449 5363 3354 ]Bd
  264096. 5391 3795 M
  264097. 5331 3691 l
  264098. 5531 3634 l
  264099. 5541 3652 l
  264100. count origstk sub{P}rp end
  264101. chemsave restore
  264102.     Helvetica
  264103. Times
  264104. 3mol%
  264105. 3mol%
  264106.     Helvetica
  264107. Times
  264108. 9swsD
  264109.     Helvetica
  264110.     Helvetica
  264111.     Helvetica
  264112.     Helvetica
  264113.     Helvetica
  264114.     Helvetica
  264115.     Helvetica
  264116.     Helvetica
  264117.     Helvetica
  264118.     Helvetica
  264119. 3mol%
  264120. Untitled Refs-22
  264121. count
  264122. currentpoint 192837465
  264123. currentpoint
  264124. save/chemsave exch def
  264125. %%BeginProcSet: chemdict30 24 10
  264126. % ChemDraw Laser Prep
  264127. % Copyright 1986-19
  264128. , CambridgeSoft Corporation
  264129. userdict/chemdict30 210 dict put
  264130. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/rm/
  264131. rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d/cW 
  264132. 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  264133. x}b/sRmp{current
  264134. rgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264135. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264136. 0 cw 2 dv xl
  264137. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  264138. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  264139. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  264140. St 16 and 0 ne{2 ix 6 m 1 a 
  264141. D ix e D ix e D ix e D ix e P SpA}if
  264142. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  264143. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  264144. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  264145. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  264146. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  264147. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc cp 
  264148. f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  264149. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  264150. P P}{sq at 2
  264151. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  264152. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  264153. l w .35 dv w -2 
  264154. m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  264155. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  264156. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  264157. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  264158. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  264159. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1 s
  264160. c 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  264161. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  264162. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  264163. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  264164. 21 -10 27 -8 27 0 cv
  264165. 27 8 21 10 9 6 cv
  264166. -3 2 -3 -2 9 -6 cv
  264167. cp}b/DLB{0 0 M -4.8 4.8 l
  264168. -8 8 -9.6 12 -9.6 16.8 cv
  264169. -9.6 21.6 -8 24.6 
  264170. -4.8 25.8 cv
  264171. -1.6 27 1.6 27 4.8 25.8 cv
  264172. 8 24.6 9.6 21.6 9.6 16.8 cv
  264173. 9.6 12 8 8 4.8 4.8 cv
  264174. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  264175. 0 Y X Y rO ac
  264176. X Y X 0 rO ac
  264177. X 0 0 0 rO ac
  264178. 0 0 0 Y rO ac
  264179. cp}b/Rc{0 0 p M
  264180. 0 Y p l
  264181. X Y p l
  264182. X 0 p l
  264183. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  264184. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  264185.  D 0 lt{n}if sq n D
  264186. CMT dtransform idtransform
  264187. e 2 m e
  264188. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  264189. 32 -0.5 0.5{gs
  264190. 13.5 0 xl
  264191. D 32 s 64 dv 13.5 m D 7 m 24 dv
  264192. -13.5 0 xl
  264193. gr}for
  264194. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  264195. 32 -0.5 0.5{gs
  264196. D 32 s 64 dv 0.65 m D
  264197. gr}for
  264198. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  264199. 32 -0.5 0.5{gs
  264200. D 32 s 64 dv D
  264201. gr}for
  264202. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  264203. 32 -0.5 0.5{gs
  264204. 0 13.5 xl
  264205. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  264206. 0 -13.5 xl
  264207. DLB f
  264208. gr}for
  264209. DLB SM st}{DLB grf}i
  264210. e}b/gRr{sh{sRmp
  264211. 32 -0.5 0.5{gs
  264212. X 2 dv Y 2 dv xl
  264213. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  264214. X -2 dv Y -2 dv xl
  264215. gr}for
  264216. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  264217. 32 -0.5 0.5{gs
  264218. X 2 dv Y 2 dv xl
  264219. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  264220. X -2 dv Y -2 dv xl
  264221. gr}for
  264222. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  264223. rev{1 -1 sc}if
  264224. 0 lW 2 m xl
  264225. D SA OA
  264226. rad 0 xl
  264227. 180 ro
  264228. 0 lW 2 m xl
  264229. SA OA}b/Aos{X Y M SM cpt xl XY e 
  264230. dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  264231. o 0 lt o 0 lt ne/rev x
  264232. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  264233. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  264234. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  264235. lp 0 p M
  264236. 0 0 0 Y lp ac
  264237. 0 Y 2 dv lp neg o lp ac
  264238. 0 Y 2 dv 0 Y lp ac
  264239. 0 Y lp Y lp ac
  264240. X lp s 0 p M
  264241. X 0 X Y lp ac
  264242. X Y 2 dv X lp a o lp ac
  264243. X Y 2 dv X Y lp ac
  264244. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA a
  264245.  arc st
  264246. np X Y s Y 2 dv
  264247. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  264248. rO D rlineto
  264249. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  264250. rO lW -2 dv a Y lW 2 dv a rO a p l
  264251. lW -2 dv Y lW 2 dv a p l
  264252. 0 Y p l X Y p l X 0 p l cp f
  264253. 0 0 p M
  264254. 0 Y p l
  264255. X Y p l
  264256. X 0 p l cp
  264257. SM st}{Rr SM st}{rO Y p M rO rO xl
  264258. 0 Y X Y rO ac
  264259. X Y X 0 rO ac
  264260. X 0 0 0 rO ac
  264261. rO neg D xl X Y 0 Y rO ac
  264262. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  264263. -1 -1 sc LB whf}{Asc gs gLB gr
  264264. -0.4 -0.4 sc LB whf
  264265. }{Asc LB gs whf gr
  264266. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  264267. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  264268. gs 3.6 12 sc gOv gr
  264269. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  264270. gs 3.6 12 sc Cr whf gr
  264271. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  264272. 0 -1 p M
  264273. 0 0 1 0 1 ac
  264274. 8 0 8 1 1 ac
  264275. 8 0 16 0 1 ac
  264276. 16 0 16 -1 1 ac
  264277. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  264278. 2 dv D sc
  264279. 1 0 M -1 0 l
  264280. 0 1 M 0 -1 l
  264281. Ast}{XY D X 
  264282. Y dt 0 0 M SM cpt xl
  264283. 2 dv D sc
  264284. 1 0 M -1 0 l
  264285. Ast}{4.5 Aos
  264286. 1 0 M -1 0 l
  264287. 0 1 M 0 -1 l
  264288. 2 0 M 0 0 2 0 360 arc
  264289. Ast}{4.5 Aos
  264290. 1 0 M -1 0 l
  264291. 2 0 M 0 0 2 0 360 arc
  264292. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  264293. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  264294. 1 -1 M -1 -1 l
  264295. 0 2 M 0 -2 l
  264296. Ast}{5 Aos
  264297. 1 -1 M -1 -1 l
  264298. 1 1 M -1 1 l
  264299. 0 2 M 0 -2 l
  264300. Ast}{4.5 Aos
  264301. 1 0 M -1 0 l
  264302. 0 1 M 0 -1 l
  264303. Ast}{4.5 Aos
  264304. 1 0 M -1 0 l
  264305. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs wh
  264306. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  264307. gs 3.6 12 sc Cr whf gr
  264308. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  264309. gs 3.6 12 sc Cr blf gr
  264310. ZLB whf}{Asc LB gs whf gr
  264311. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  264312. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  264313. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  264314. e 2 ix a}b/PT{D 2 4 
  264315. gi al P OP D 1 sc
  264316. o length 6 gt{P 6 g}{e P 8 dv}ie
  264317. D lW 2 m lt{P lW 2 m}if
  264318. 0 e p
  264319. 0 0 p
  264320. 3 -1 r s 3 1 r e s e
  264321. 0 0 p M 1 0 p l
  264322. 0 0 p ap M 1 0 p ap l
  264323. e n e n
  264324. 0 0 p ap M 1 0 p ap l
  264325. P P}b/DT{gs np PT SM st gr}b
  264326. O/NH{lW s D hS dv ru
  264327. cvi D 0 eq{P 1}if/nH x
  264328. D hS nH m s
  264329. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  264330. bW 2 dv/bd x
  264331. lW 2 dv e D NH e{D bd p M bd n p l}for
  264332. st gr}{gs 12 OB np
  264333. lW 2 dv 0 xl NH 1 sc
  264334. bW 2 dv wF m nH 1 a d
  264335. v/bd x
  264336. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  264337. np 0 lW 2 dv o o n p M p l bW 2 dv
  264338. wF m o o p l n p l
  264339. cp f gr}{P}{gs 12 OB/bL x
  264340. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  264341. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  264342. bL nSq 2 m dv D sc
  264343. nSq{.135  .667 .865  .667 1 0 rcurveto
  264344. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  264345. np 0 lW 2 dv o o n p M p l bW 2 dv
  264346. wF m o o p l n p l
  264347. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  264348. 5 -1 r 
  264349. xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  264350. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  264351. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  264352. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  264353. 5 -1 r dv neg e 5 -1 r dv neg e
  264354. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  264355. %%EndProcSet
  264356. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  264357. 283 146 91 87 SPn/origstk x
  264358. 5535 65535 65535 sBg
  264359. 0 0 0 C
  264360. 1900 3394 M
  264361. 1880 3406 l
  264362. 1880 2794 l
  264363. 1900 2806 l
  264364. 1972 3358 M
  264365. 1952 3358 l
  264366. 1952 2842 l
  264367. 1972 2842 l
  264368. 2410 3688 M
  264369. 2410 3712 l
  264370. 1880 3406 l
  264371. 1900 3394 l
  264372. 2920 3394 M
  264373. 2930 3400 l
  264374. 2931 3411 l
  264375. 2410 3712 l
  264376. 2410 3688 l
  264377. 2853 3349 M
  264378. 2863 3367 l
  264379. 2415 3626 l
  264380. 2405 3608 l
  264381. 2920 2806 M
  264382. 2930 2800 l
  264383. 2940 2808 l
  264384. 2940 3392 l
  264385. 2930 3400 l
  264386. 2920 3394 l
  264387. 2410 2512 M
  264388. 2410 2488 l
  264389. 2931 2789 l
  264390. 2930 2800 l
  264391. 2920 2806 l
  264392. 2405 2592 M
  264393. 2415 2574 
  264394. 2863 2833 l
  264395. 2853 2851 l
  264396. 2410 2488 M
  264397. 2410 2512 l
  264398. 1900 2806 l
  264399. 1880 2794 l
  264400. 3497 3573 M
  264401. 3505 3597 l
  264402. 2931 3411 l
  264403. 2930 3400 l
  264404. 2940 3392 l
  264405. 3750 3224 M
  264406. 3766 3236 l
  264407. 3505 3597 l
  264408. 3497 3573 l
  264409. 3537 2680 M
  264410. 3553 2668 l
  264411. 3766 2963 l
  264412. 3750 2975 l
  264413. 3406 2634 M
  264414. 3412 2654 l
  264415. 2940 2808 l
  264416. 2930 2800 l
  264417. 2931 2789 l
  264418. 3987 3557 M
  264419. 3967 3563 l
  264420. 3878 3233 l
  264421. 3898 3227 l
  264422. 4529 3968 M
  264423. 4528 3979 l
  264424. 4517 3985 l
  264425. 4105 3747 l
  264426. 4115 3729 l
  264427. 4986 3845 M
  264428. 4992 3865 l
  264429. 4537 398
  264430. 4528 3979 l
  264431. 4529 3968 l
  264432. 5353 3378 M
  264433. 5371 3388 l
  264434. 5176 3725 l
  264435. 5158 3715 l
  264436. 5272 2839 M
  264437. 5292 2833 l
  264438. 5383 3167 l
  264439. 5363 3173 l
  264440. 4731 2434 M
  264441. 4732 2423 l
  264442. 4743 2417 l
  264443. 5135 2644 l
  264444. 5125 2662 l
  264445. 4275 2557 M
  264446. 4269 2537 l
  264447. 4723 2415 l
  264448. 4732 2423 l
  264449. 4731 2434 l
  264450. 4080 2685 M
  264451. 4098 2695 l
  264452. 3916 3010 l
  264453. 3898 3000 l
  264454. 5640 3712 M
  264455. 5622 3722 l
  264456. 5471 3443 l
  264457. 5489 3433 l
  264458. 6267 3713 M
  264459. 6276 3722 l
  264460. 6274 3733 l
  264461. 5773 3823 l
  264462. 5769 3803 l
  264463. 6345 3138 M
  264464. 6356 3132 l
  264465. 6365 3
  264466. 139 l
  264467. 6287 3718 l
  264468. 6276 3722 l
  264469. 6267 3713 l
  264470. 6412 3182 M
  264471. 6432 3184 l
  264472. 6363 3691 l
  264473. 6343 3689 l
  264474. 5822 2886 M
  264475. 5818 2862 l
  264476. 6356 3121 l
  264477. 6356 3132 l
  264478. 6345 3138 l
  264479. 5818 2862 M
  264480. 5822 2886 l
  264481. 5532 3188 l
  264482. 5518 3174 l
  264483. 6749 4075 M
  264484. 6745 4097 l
  264485. 6274 3733 l
  264486. 6276 3722 l
  264487. 6287 3718 l
  264488. 7289 3853 M
  264489. 7307 3867 l
  264490. 6745 4097 l
  264491. 6749 4075 l
  264492. 7229 3801 M
  264493. 7237 3819 l
  264494. 6762 4014 l
  264495. 6754 3996 l
  264496. 7367 3274 M
  264497. 7389 3266 l
  264498. 7307 3867 l
  264499. 7289 3853 l
  264500. 6905 2917 M
  264501. 6909 2895 l
  264502.  3266 l
  264503. 7367 3274 l
  264504. 6890 2996 M
  264505. 6902 2980 l
  264506. 7307 3294 l
  264507. 7295 3310 l
  264508. 6909 2895 M
  264509. 6905 2917 l
  264510. 6365 3139 l
  264511. 6356 3132 l
  264512. 6356 3121 l
  264513. 4800 1827 M
  264514. 4820 1829 l
  264515. 4743 2417 l
  264516. 4732 2423 l
  264517. 4723 2415 l
  264518. 4460 4575 M
  264519. 4440 4573 l
  264520. 4517 3985 l
  264521. 4528 3979 l
  264522. 4537 3987 l
  264523. 3635 2167 M
  264524. 3655 2173 l
  264525. 3547 2506 l
  264526. 3527 2500 l
  264527. 3259 2216 M
  264528. 3277 2206 l
  264529. 3447 2500 l
  264530. 3429 2510 l
  264531. 5492 4259 M
  264532. 5474 4251 l
  264533. 5618 3955 l
  264534. 5636 3963 l
  264535. 5819 4268 M
  264536. 5799 4274 l
  264537. 5699 3905 l
  264538. 19 3899 l
  264539. 5098 2880 4624 3154 38 Ar
  264540. 4169 3587 4614 3201 38 Ar
  264541. count origstk sub{P}rp end
  264542. chemsave restore
  264543.     Helvetica
  264544.     Helvetica
  264545.     Helvetica
  264546.     Helvetica
  264547.     Helvetica
  264548.     Helvetica
  264549.     Helvetica
  264550.     Helvetica
  264551.     Helvetica
  264552.     Helvetica
  264553.     Helvetica
  264554.     Helvetica
  264555.     Helvetica
  264556.     Helvetica
  264557.     Helvetica
  264558. Untitled Refs-3
  264559. count
  264560. currentpoint 192837465
  264561. currentpoint
  264562. save/chemsave exch def
  264563. %%BeginProcSet: chemdict30 24 10
  264564. % ChemDraw Laser Prep
  264565. % Copyright 1986-1995
  264566. 95, CambridgeSoft Corporation
  264567. userdict/chemdict30 210 dict put
  264568. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/r
  264569. m/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d/c
  264570. W 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  264571. x}b/sRmp{curre
  264572. ntrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264573. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264574. 0 cw 2 dv xl
  264575. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  264576. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  264577. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  264578. St 16 and 0 ne{2 ix 6 m 1 
  264579. a D ix e D ix e D ix e D ix e P SpA}if
  264580. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  264581. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  264582. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  264583. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  264584. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  264585. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc c
  264586. p f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  264587. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  264588. P P}{sq at 2
  264589. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  264590. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  264591. l w .35 dv w -
  264592. 2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  264593. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  264594. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  264595. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  264596. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  264597. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1
  264598.  sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  264599. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  264600. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  264601. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  264602. 21 -10 27 -8 27 0 cv
  264603. 27 8 21 10 9 6 cv
  264604. -3 2 -3 -2 9 -6 cv
  264605. cp}b/DLB{0 0 M -4.8 4.8 l
  264606. -8 8 -9.6 12 -9.6 16.8 cv
  264607. -9.6 21.6 -8 24.
  264608. 6 -4.8 25.8 cv
  264609. -1.6 27 1.6 27 4.8 25.8 cv
  264610. 8 24.6 9.6 21.6 9.6 16.8 cv
  264611. 9.6 12 8 8 4.8 4.8 cv
  264612. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  264613. 0 Y X Y rO ac
  264614. X Y X 0 rO ac
  264615. X 0 0 0 rO ac
  264616. 0 0 0 Y rO ac
  264617. cp}b/Rc{0 0 p M
  264618. 0 Y p l
  264619. X Y p l
  264620. X 0 p l
  264621. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  264622. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  264623. m D 0 lt{n}if sq n D
  264624. CMT dtransform idtransform
  264625. e 2 m e
  264626. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  264627. 32 -0.5 0.5{gs
  264628. 13.5 0 xl
  264629. D 32 s 64 dv 13.5 m D 7 m 24 dv
  264630. -13.5 0 xl
  264631. gr}for
  264632. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  264633. 32 -0.5 0.5{gs
  264634. D 32 s 64 dv 0.65 m D
  264635. gr}for
  264636. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  264637. 32 -0.5 0.5{gs
  264638. D 32 s 64 dv D
  264639. gr}for
  264640. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  264641. 32 -0.5 0.5{gs
  264642. 0 13.5 xl
  264643. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  264644. 0 -13.5 xl
  264645. DLB f
  264646. gr}for
  264647. DLB SM st}{DLB grf
  264648. }ie}b/gRr{sh{sRmp
  264649. 32 -0.5 0.5{gs
  264650. X 2 dv Y 2 dv xl
  264651. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  264652. X -2 dv Y -2 dv xl
  264653. gr}for
  264654. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  264655. 32 -0.5 0.5{gs
  264656. X 2 dv Y 2 dv xl
  264657. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  264658. X -2 dv Y -2 dv xl
  264659. gr}for
  264660. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  264661. rev{1 -1 sc}if
  264662. 0 lW 2 m xl
  264663. D SA OA
  264664. rad 0 xl
  264665. 180 ro
  264666. 0 lW 2 m xl
  264667. SA OA}b/Aos{X Y M SM cpt xl XY 
  264668. e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  264669. o 0 lt o 0 lt ne/rev x
  264670. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  264671. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  264672. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  264673. lp 0 p M
  264674. 0 0 0 Y lp ac
  264675. 0 Y 2 dv lp neg o lp ac
  264676. 0 Y 2 dv 0 Y lp ac
  264677. 0 Y lp Y lp ac
  264678. X lp s 0 p M
  264679. X 0 X Y lp ac
  264680. X Y 2 dv X lp a o lp ac
  264681. X Y 2 dv X Y lp ac
  264682. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA
  264683.  a arc st
  264684. np X Y s Y 2 dv
  264685. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  264686. rO D rlineto
  264687. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  264688. rO lW -2 dv a Y lW 2 dv a rO a p l
  264689. lW -2 dv Y lW 2 dv a p l
  264690. 0 Y p l X Y p l X 0 p l cp f
  264691. 0 0 p M
  264692. 0 Y p l
  264693. X Y p l
  264694. X 0 p l cp
  264695. SM st}{Rr SM st}{rO Y p M rO rO xl
  264696. 0 Y X Y rO ac
  264697. X Y X 0 rO ac
  264698. X 0 0 0 rO ac
  264699. rO neg D xl X Y 0 Y rO ac
  264700. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  264701. -1 -1 sc LB whf}{Asc gs gLB gr
  264702. -0.4 -0.4 sc LB w
  264703. hf}{Asc LB gs whf gr
  264704. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  264705. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  264706. gs 3.6 12 sc gOv gr
  264707. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  264708. gs 3.6 12 sc Cr whf gr
  264709. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  264710. 0 -1 p M
  264711. 0 0 1 0 1 ac
  264712. 8 0 8 1 1 ac
  264713. 8 0 16 0 1 ac
  264714. 16 0 16 -1 1 ac
  264715. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  264716. 2 dv D sc
  264717. 1 0 M -1 0 l
  264718. 0 1 M 0 -1 l
  264719. Ast}{XY D 
  264720. X Y dt 0 0 M SM cpt xl
  264721. 2 dv D sc
  264722. 1 0 M -1 0 l
  264723. Ast}{4.5 Aos
  264724. 1 0 M -1 0 l
  264725. 0 1 M 0 -1 l
  264726. 2 0 M 0 0 2 0 360 arc
  264727. Ast}{4.5 Aos
  264728. 1 0 M -1 0 l
  264729. 2 0 M 0 0 2 0 360 arc
  264730. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  264731. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  264732. 1 -1 M -1 -1 l
  264733. 0 2 M 0 -2 l
  264734. Ast}{5 Aos
  264735. 1 -1 M -1 -1 l
  264736. 1 1 M -1 1 l
  264737. 0 2 M 0 -2 l
  264738. Ast}{4.5 Aos
  264739. 1 0 M -1 0 l
  264740. 0 1 M 0 -1 l
  264741. Ast}{4.5 Aos
  264742. 1 0 M -1 0 l
  264743. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs 
  264744. whf gr
  264745. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  264746. gs 3.6 12 sc Cr whf gr
  264747. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  264748. gs 3.6 12 sc Cr blf gr
  264749. ZLB whf}{Asc LB gs whf gr
  264750. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  264751. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  264752. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  264753. e 2 ix a}b/PT{D 2 
  264754. 4 gi al P OP D 1 sc
  264755. o length 6 gt{P 6 g}{e P 8 dv}ie
  264756. D lW 2 m lt{P lW 2 m}if
  264757. 0 e p
  264758. 0 0 p
  264759. 3 -1 r s 3 1 r e s e
  264760. 0 0 p M 1 0 p l
  264761. 0 0 p ap M 1 0 p ap l
  264762. e n e n
  264763. 0 0 p ap M 1 0 p ap l
  264764. P P}b/DT{gs np PT SM st gr}b
  264765. O/NH{lW s D hS dv ru
  264766. cvi D 0 eq{P 1}if/nH x
  264767. D hS nH m s
  264768. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  264769. bW 2 dv/bd x
  264770. lW 2 dv e D NH e{D bd p M bd n p l}for
  264771. st gr}{gs 12 OB np
  264772. lW 2 dv 0 xl NH 1 sc
  264773. bW 2 dv wF m nH 1 a
  264774.  dv/bd x
  264775. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  264776. np 0 lW 2 dv o o n p M p l bW 2 dv
  264777. wF m o o p l n p l
  264778. cp f gr}{P}{gs 12 OB/bL x
  264779. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  264780. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  264781. bL nSq 2 m dv D sc
  264782. nSq{.135  .667 .865  .667 1 0 rcurveto
  264783. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  264784. np 0 lW 2 dv o o n p M p l bW 2 dv
  264785. wF m o o p l n p l
  264786. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  264787. 5 -1 
  264788. r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  264789. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  264790. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  264791. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  264792. 5 -1 r dv neg e 5 -1 r dv neg e
  264793. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  264794. %%EndProcSet
  264795. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  264796. 527 304 33 113 SPn/origstk x
  264797. 65535 65535 65535 sBg
  264798. 0 0 0 C
  264799. 8400 3248 M
  264800. 8400 3272 l
  264801. 7964 3020 l
  264802. 7974 3002 l
  264803. 8920 2948 M
  264804. 8920 2972 l
  264805. 8400 3272 l
  264806. 8400 3248 l
  264807. 9440 3248 M
  264808. 9440 3272 l
  264809. 8920 2972 l
  264810. 8920 2948 l
  264811. 9960 2948 M
  264812. 9960 2972 l
  264813. 9440 3272 l
  264814. 9440 3248 l
  264815. 10480 3248 M
  264816. 10480 3272 l
  264817. 9960 2972 l
  264818. 9960 29
  264819. 9486 3750 M
  264820. 9466 3750 l
  264821. 9466 3240 l
  264822. 9486 3240 l
  264823. 9414 3750 M
  264824. 9394 3750 l
  264825. 9394 3240 l
  264826. 9414 3240 l
  264827. f[1 4 8920 2907 8920 2480 ]Bd
  264828. 10873 3021 M
  264829. 10883 3039 l
  264830. 10480 3272 l
  264831. 10480 3248 l
  264832. 1740 4128 M
  264833. 1740 4152 l
  264834. 1304 3900 l
  264835. 1314 3882 l
  264836. 2260 3828 M
  264837. 2260 3852 l
  264838. 1740 4152 l
  264839. 1740 4128 l
  264840. 2780 4128 M
  264841. 2780 4152 l
  264842. 2260 3852 l
  264843. 2260 3828 l
  264844. 3300 3828 M
  264845. 3300 3852 l
  264846. 2780 4152 l
  264847. 2780 4128 l
  264848. 3825 4131 M
  264849. 3815 4149 l
  264850. 3300 3852 l
  264851. 3300 3828 l
  264852. 3789 4193 M
  264853. 3779 4211 l
  264854. 3295 3932 l
  264855. 3305 3914 l
  264856. f[1 4 2780 4193 2780 4620 ]Bd
  264857. [1 4 2260 3787 2260 3360 ]Bd
  264858. 8300 6468 M
  264859. 8300 6492 l
  264860. 7864 6240 l
  264861. 7874 6222 l
  264862. 8820 6168 M
  264863. 8820 6192 l
  264864. 8300 6492 l
  264865. 8300 6468 l
  264866. 9340 6468 M
  264867. 9340 6492 l
  264868. 8820 6192 l
  264869. 8820 6168 l
  264870. 9860 6168 M
  264871. 9860 6192 l
  264872. 9340 6492 l
  264873. 9340 6468 l
  264874. 10380 6468 M
  264875. 10380 6492 l
  264876. 9860 6192 l
  264877. 9860 6168 l
  264878. 10385 6388 M
  264879. 10375 6406 l
  264880. 9891 6127 l
  264881. 9901 6109 l
  264882. f[1 4 9340 6533 9340 6960 ]Bd
  264883. [1 4 8820 6127 
  264884. 8820 5700 ]Bd
  264885. 10773 6241 M
  264886. 10783 6259 l
  264887. 10380 6492 l
  264888. 10380 6468 l
  264889. 7186 3092 4990 3680 2 Ar
  264890. 6786 5721 4810 4580 2 Ar
  264891. count origstk sub{P}rp end
  264892. chemsave restore
  264893.     Helvetica
  264894. Times
  264895. Pd(OAc)
  264896. mol%)
  264897. 20mol%)
  264898. DMF 100
  264899. Conditions = 
  264900. JCHMD
  264901. !Pd(OAc)2 (10mol%)
  264902. nBu3P  (20mol%)
  264903. DMF 100oC
  264904. K2CO3
  264905. Conditions = 
  264906.     Helvetica
  264907. Times
  264908. *swsD
  264909.     Helvetica
  264910.     Helvetica
  264911. MPMO^
  264912.     Helvetica
  264913.     Helvetica
  264914.     Helvetica
  264915.     Helvetica
  264916. MPMO^
  264917.     Helvetica
  264918.     Helvetica
  264919.     Helvetica
  264920. MPMO^
  264921.     Helvetica
  264922.     Helvetica
  264923.     Helvetica
  264924. !Pd(OA
  264925. c)2 (10mol%)
  264926. nBu3P  (20mol%)
  264927. DMF 100oC
  264928. K2CO3
  264929. Conditions = 
  264930. Untitled Document-4
  264931. count
  264932. currentpoint 192837465
  264933. currentpoint
  264934. save/chemsave exch def
  264935. %%BeginProcSet: chemdict30 24 10
  264936. % ChemDraw Laser Prep
  264937. % Copyright 1986-
  264938. , CambridgeSoft Corporation
  264939. userdict/chemdict30 210 dict put
  264940. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/rm/
  264941. rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d/cW 
  264942. 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  264943. x}b/sRmp{current
  264944. rgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264945. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  264946. 0 cw 2 dv xl
  264947. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  264948. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  264949. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  264950. St 16 and 0 ne{2 ix 6 m 1 a 
  264951. D ix e D ix e D ix e D ix e P SpA}if
  264952. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  264953. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  264954. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  264955. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  264956. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  264957. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc cp 
  264958. f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  264959. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  264960. P P}{sq at 2
  264961. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  264962. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  264963. l w .35 dv w -2 
  264964. m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  264965. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  264966. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  264967. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  264968. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  264969. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1 s
  264970. c 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  264971. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  264972. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  264973. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  264974. 21 -10 27 -8 27 0 cv
  264975. 27 8 21 10 9 6 cv
  264976. -3 2 -3 -2 9 -6 cv
  264977. cp}b/DLB{0 0 M -4.8 4.8 l
  264978. -8 8 -9.6 12 -9.6 16.8 cv
  264979. -9.6 21.6 -8 24.6 
  264980. -4.8 25.8 cv
  264981. -1.6 27 1.6 27 4.8 25.8 cv
  264982. 8 24.6 9.6 21.6 9.6 16.8 cv
  264983. 9.6 12 8 8 4.8 4.8 cv
  264984. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  264985. 0 Y X Y rO ac
  264986. X Y X 0 rO ac
  264987. X 0 0 0 rO ac
  264988. 0 0 0 Y rO ac
  264989. cp}b/Rc{0 0 p M
  264990. 0 Y p l
  264991. X Y p l
  264992. X 0 p l
  264993. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  264994. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  264995.  D 0 lt{n}if sq n D
  264996. CMT dtransform idtransform
  264997. e 2 m e
  264998. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  264999. 32 -0.5 0.5{gs
  265000. 13.5 0 xl
  265001. D 32 s 64 dv 13.5 m D 7 m 24 dv
  265002. -13.5 0 xl
  265003. gr}for
  265004. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  265005. 32 -0.5 0.5{gs
  265006. D 32 s 64 dv 0.65 m D
  265007. gr}for
  265008. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  265009. 32 -0.5 0.5{gs
  265010. D 32 s 64 dv D
  265011. gr}for
  265012. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  265013. 32 -0.5 0.5{gs
  265014. 0 13.5 xl
  265015. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  265016. 0 -13.5 xl
  265017. DLB f
  265018. gr}for
  265019. DLB SM st}{DLB grf}i
  265020. e}b/gRr{sh{sRmp
  265021. 32 -0.5 0.5{gs
  265022. X 2 dv Y 2 dv xl
  265023. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  265024. X -2 dv Y -2 dv xl
  265025. gr}for
  265026. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  265027. 32 -0.5 0.5{gs
  265028. X 2 dv Y 2 dv xl
  265029. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  265030. X -2 dv Y -2 dv xl
  265031. gr}for
  265032. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  265033. rev{1 -1 sc}if
  265034. 0 lW 2 m xl
  265035. D SA OA
  265036. rad 0 xl
  265037. 180 ro
  265038. 0 lW 2 m xl
  265039. SA OA}b/Aos{X Y M SM cpt xl XY e 
  265040. dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  265041. o 0 lt o 0 lt ne/rev x
  265042. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
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  265044. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  265045. lp 0 p M
  265046. 0 0 0 Y lp ac
  265047. 0 Y 2 dv lp neg o lp ac
  265048. 0 Y 2 dv 0 Y lp ac
  265049. 0 Y lp Y lp ac
  265050. X lp s 0 p M
  265051. X 0 X Y lp ac
  265052. X Y 2 dv X lp a o lp ac
  265053. X Y 2 dv X Y lp ac
  265054. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA a
  265055.  arc st
  265056. np X Y s Y 2 dv
  265057. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  265058. rO D rlineto
  265059. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  265060. rO lW -2 dv a Y lW 2 dv a rO a p l
  265061. lW -2 dv Y lW 2 dv a p l
  265062. 0 Y p l X Y p l X 0 p l cp f
  265063. 0 0 p M
  265064. 0 Y p l
  265065. X Y p l
  265066. X 0 p l cp
  265067. SM st}{Rr SM st}{rO Y p M rO rO xl
  265068. 0 Y X Y rO ac
  265069. X Y X 0 rO ac
  265070. X 0 0 0 rO ac
  265071. rO neg D xl X Y 0 Y rO ac
  265072. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  265073. -1 -1 sc LB whf}{Asc gs gLB gr
  265074. -0.4 -0.4 sc LB whf
  265075. }{Asc LB gs whf gr
  265076. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  265077. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  265078. gs 3.6 12 sc gOv gr
  265079. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  265080. gs 3.6 12 sc Cr whf gr
  265081. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  265082. 0 -1 p M
  265083. 0 0 1 0 1 ac
  265084. 8 0 8 1 1 ac
  265085. 8 0 16 0 1 ac
  265086. 16 0 16 -1 1 ac
  265087. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  265088. 2 dv D sc
  265089. 1 0 M -1 0 l
  265090. 0 1 M 0 -1 l
  265091. Ast}{XY D X 
  265092. Y dt 0 0 M SM cpt xl
  265093. 2 dv D sc
  265094. 1 0 M -1 0 l
  265095. Ast}{4.5 Aos
  265096. 1 0 M -1 0 l
  265097. 0 1 M 0 -1 l
  265098. 2 0 M 0 0 2 0 360 arc
  265099. Ast}{4.5 Aos
  265100. 1 0 M -1 0 l
  265101. 2 0 M 0 0 2 0 360 arc
  265102. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  265103. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  265104. 1 -1 M -1 -1 l
  265105. 0 2 M 0 -2 l
  265106. Ast}{5 Aos
  265107. 1 -1 M -1 -1 l
  265108. 1 1 M -1 1 l
  265109. 0 2 M 0 -2 l
  265110. Ast}{4.5 Aos
  265111. 1 0 M -1 0 l
  265112. 0 1 M 0 -1 l
  265113. Ast}{4.5 Aos
  265114. 1 0 M -1 0 l
  265115. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs wh
  265116. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  265117. gs 3.6 12 sc Cr whf gr
  265118. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  265119. gs 3.6 12 sc Cr blf gr
  265120. ZLB whf}{Asc LB gs whf gr
  265121. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  265122. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  265123. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  265124. e 2 ix a}b/PT{D 2 4 
  265125. gi al P OP D 1 sc
  265126. o length 6 gt{P 6 g}{e P 8 dv}ie
  265127. D lW 2 m lt{P lW 2 m}if
  265128. 0 e p
  265129. 0 0 p
  265130. 3 -1 r s 3 1 r e s e
  265131. 0 0 p M 1 0 p l
  265132. 0 0 p ap M 1 0 p ap l
  265133. e n e n
  265134. 0 0 p ap M 1 0 p ap l
  265135. P P}b/DT{gs np PT SM st gr}b
  265136. O/NH{lW s D hS dv ru
  265137. cvi D 0 eq{P 1}if/nH x
  265138. D hS nH m s
  265139. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  265140. bW 2 dv/bd x
  265141. lW 2 dv e D NH e{D bd p M bd n p l}for
  265142. st gr}{gs 12 OB np
  265143. lW 2 dv 0 xl NH 1 sc
  265144. bW 2 dv wF m nH 1 a d
  265145. v/bd x
  265146. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  265147. np 0 lW 2 dv o o n p M p l bW 2 dv
  265148. wF m o o p l n p l
  265149. cp f gr}{P}{gs 12 OB/bL x
  265150. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  265151. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  265152. bL nSq 2 m dv D sc
  265153. nSq{.135  .667 .865  .667 1 0 rcurveto
  265154. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  265155. np 0 lW 2 dv o o n p M p l bW 2 dv
  265156. wF m o o p l n p l
  265157. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  265158. 5 -1 r 
  265159. xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  265160. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  265161. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  265162. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  265163. 5 -1 r dv neg e 5 -1 r dv neg e
  265164. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  265165. %%EndProcSet
  265166. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  265167. 712 181 3 166 SPn/origstk x
  265168. 65535 65535 65535 sBg
  265169. 0 0 0 C
  265170. 150 5044 M
  265171. 130 5056 l
  265172. 130 4444 l
  265173. 150 4456 l
  265174. 222 5008 M
  265175. 202 5008 l
  265176. 202 4492 l
  265177. 222 4492 l
  265178. 660 5338 M
  265179. 660 5362 l
  265180. 130 5056 l
  265181. 150 5044 l
  265182. 1170 5044 M
  265183. 1180 5050 
  265184. 1180 5062 l
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  265186. 660 5338 l
  265187. 1103 4999 M
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  265190. 655 5258 l
  265191. 1170 4456 M
  265192. 1180 4450 l
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  265194. 1190 5044 l
  265195. 1180 5050 l
  265196. 1170 5044 l
  265197. 660 4162 M
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  265199. 1180 4438 l
  265200. 1180 4450 l
  265201. 1170 4456 l
  265202. 655 4242 M
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  265205. 1103 4501 l
  265206. 660 4138 M
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  265209. 130 4444 l
  265210. 1569 4213 M
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  265212. 1190 4456 l
  265213. 1180 4450 l
  265214. 1180 4438 l
  265215. 1595 5278 M
  265216. 1585 5296 l
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  265218. 1180 5050 l
  265219. 1190 5044 l
  265220. 2190 534
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  265222. 1790 5360 l
  265223. 1790 5340 l
  265224. 2190 5412 M
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  265226. 1790 5432 l
  265227. 1790 5412 l
  265228. 2190 5268 M
  265229. 2190 5288 l
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  265231. 1790 5268 l
  265232. 2780 5340 M
  265233. 2780 5360 l
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  265235. 2390 5340 l
  265236. 5303 4610 3040 4610 2 Ar
  265237. 5390 4924 M
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  265239. 5370 4324 l
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  265245. 5900 5218 M
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  265249. 6410 4924 M
  265250. 6420 4930 l
  265251. 6421 4941 l
  265252. 5900 5242 l
  265253. 5900 5218 l
  265254. 6343 4879 M
  265255.  4897 l
  265256. 5905 5156 l
  265257. 5895 5138 l
  265258. 6410 4336 M
  265259. 6420 4330 l
  265260. 6430 4338 l
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  265262. 6420 4930 l
  265263. 6410 4924 l
  265264. 5900 4042 M
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  265281. 6420 4930 l
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  265283. 7331 4629 M
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  265286. 6991 5115 l
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  265288. 7061 4258 M
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  265290. 7355 4629 l
  265291. 7331 4629 
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  265296. 6421 4319 l
  265297. 7123 3703 M
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  265300. 7022 4013 l
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  265305. 7830 4655 M
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  265307. 7317 4675 l
  265308. 7317 4655 l
  265309. 7189 5687 M
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  265313. 7002 5116 l
  265314. 6888 6021 M
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  265316. 7165 5683 l
  265317. 7189 5687 l
  265318. 8590 4954 M
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  265321. 8590 4366 l
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  265335. 9543 4909 M
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  265339. 9610 4366 M
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  265343. 9620 4960 l
  265344. 9610 4954 l
  265345. 9100 4072 M
  265346. 9100 4048 l
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  265348. 9620 4360 l
  265349. 9610 4366 l
  265350. 9095 4152 M
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  265354. 9100 4048 M
  265355. 9100 4072 l
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  265363. 0 4952 l
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  265373. 10086 4197 M
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  265443. 13080 5278 M
  265444. 13080 5302 l
  265445. 12560 5002 l
  265446. 12560 4990 l
  265447. 12570 4984 l
  265448. 13590 4984 M
  265449. 13600 4990 l
  265450. 13600 5002 l
  265451. 13080 
  265452. O5302 l
  265453. 13080 5278 l
  265454. 13523 4939 M
  265455. 13533 4957 l
  265456. 13085 5216 l
  265457. 13075 5198 l
  265458. 13590 4396 M
  265459. 13610 4
  265460. 384 l
  265461. 13610 4984 l
  265462. 13600 4990 l
  265463. 13590 4984 l
  265464. 13165 4151 M
  265465. 13175 4133 l
  265466. 13610 4384 l
  265467. 13590 4396 l
  265468. 12965 4144 M
  265469. 12975 4162 l
  265470. 12570 4396 l
  265471. 12560 4390 l
  265472. 12560 4378 l
  265473. 13070 3620 M
  265474. 13090 3620 l
  265475. 13090 3990 l
  265476. 13070 3990 l
  265477. 13984 4115 M
  265478. 13994 4133 l
  265479. 13570 4379 l
  265480. 13560 4361 l
  265481. 14020 4177 M
  265482. 14030 4195 l
  265483. 13605 4440 l
  265484. 13595 4422 l
  265485. 14008 5214 M
  265486. 13998 5232 l
  265487. 13600 5002 l
  265488. 13600 4990 l
  265489. 13610 4984 l
  265490. count origstk sub{P}rp end
  265491. chemsave restore
  265492.     Helvetica
  265493. Times
  265494. CO  +  H
  265495. O / Dioxane
  265496.   Cat.
  265497. CO  +  H2O / Dioxane
  265498. Rh6(CO)16  Cat.
  265499.     Helvetica
  265500. Times
  265501. elvetica
  265502.     Helvetica
  265503.     Helvetica
  265504.     Helvetica
  265505.     Helvetica
  265506.     Helvetica
  265507.     Helvetica
  265508.     Helvetica
  265509.     Helvetica
  265510.     Helvetica
  265511.     Helvetica
  265512.     Helvetica
  265513.     Helvetica
  265514.     Helvetica
  265515.     Helvetica
  265516.     Helvetica
  265517.     Helvetica
  265518. CO  +  H2O / Dioxane
  265519. Rh6(CO)16  Cat.
  265520. Untitled Refs-6
  265521. count
  265522. currentpoint 192837465
  265523. currentpoint
  265524. save/chemsave exch def
  265525. %%BeginProcSet: chemdict30 24 10
  265526. % ChemDraw Laser Prep
  265527. % Copyright 1986-1995
  265528. 1995, CambridgeSoft Corporation
  265529. userdict/chemdict30 210 dict put
  265530. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L
  265531. /rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d
  265532. /cW 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  265533. x}b/sRmp{cur
  265534. rentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  265535. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  265536. 0 cw 2 dv xl
  265537. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  265538. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  265539. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  265540. St 16 and 0 ne{2 ix 6 m 
  265541. 1 a D ix e D ix e D ix e D ix e P SpA}if
  265542. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  265543. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  265544. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  265545. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  265546. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  265547. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc
  265548.  cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  265549. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  265550. P P}{sq at 2
  265551. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  265552. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  265553. l w .35 dv w
  265554.  -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  265555. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  265556. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  265557. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  265558. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  265559. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 
  265560. -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  265561. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  265562. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  265563. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  265564. 21 -10 27 -8 27 0 cv
  265565. 27 8 21 10 9 6 cv
  265566. -3 2 -3 -2 9 -6 cv
  265567. cp}b/DLB{0 0 M -4.8 4.8 l
  265568. -8 8 -9.6 12 -9.6 16.8 cv
  265569. -9.6 21.6 -8 2
  265570. 4.6 -4.8 25.8 cv
  265571. -1.6 27 1.6 27 4.8 25.8 cv
  265572. 8 24.6 9.6 21.6 9.6 16.8 cv
  265573. 9.6 12 8 8 4.8 4.8 cv
  265574. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  265575. 0 Y X Y rO ac
  265576. X Y X 0 rO ac
  265577. X 0 0 0 rO ac
  265578. 0 0 0 Y rO ac
  265579. cp}b/Rc{0 0 p M
  265580. 0 Y p l
  265581. X Y p l
  265582. X 0 p l
  265583. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  265584. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransfo
  265585. m D 0 lt{n}if sq n D
  265586. CMT dtransform idtransform
  265587. e 2 m e
  265588. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  265589. 32 -0.5 0.5{gs
  265590. 13.5 0 xl
  265591. D 32 s 64 dv 13.5 m D 7 m 24 dv
  265592. -13.5 0 xl
  265593. gr}for
  265594. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  265595. 32 -0.5 0.5{gs
  265596. D 32 s 64 dv 0.65 m D
  265597. gr}for
  265598. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  265599. 32 -0.5 0.5{gs
  265600. D 32 s 64 dv D
  265601. gr}for
  265602. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  265603. 32 -0.5 0.5{gs
  265604. 0 13.5 xl
  265605. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  265606. 0 -13.5 xl
  265607. DLB f
  265608. gr}for
  265609. DLB SM st}{DLB g
  265610. rf}ie}b/gRr{sh{sRmp
  265611. 32 -0.5 0.5{gs
  265612. X 2 dv Y 2 dv xl
  265613. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  265614. X -2 dv Y -2 dv xl
  265615. gr}for
  265616. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  265617. 32 -0.5 0.5{gs
  265618. X 2 dv Y 2 dv xl
  265619. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  265620. X -2 dv Y -2 dv xl
  265621. gr}for
  265622. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  265623. rev{1 -1 sc}if
  265624. 0 lW 2 m xl
  265625. D SA OA
  265626. rad 0 xl
  265627. 180 ro
  265628. 0 lW 2 m xl
  265629. SA OA}b/Aos{X Y M SM cpt xl X
  265630. Y e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  265631. o 0 lt o 0 lt ne/rev x
  265632. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  265633. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  265634. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  265635. lp 0 p M
  265636. 0 0 0 Y lp ac
  265637. 0 Y 2 dv lp neg o lp ac
  265638. 0 Y 2 dv 0 Y lp ac
  265639. 0 Y lp Y lp ac
  265640. X lp s 0 p M
  265641. X 0 X Y lp ac
  265642. X Y 2 dv X lp a o lp ac
  265643. X Y 2 dv X Y lp ac
  265644. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 
  265645. pA a arc st
  265646. np X Y s Y 2 dv
  265647. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  265648. rO D rlineto
  265649. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  265650. rO lW -2 dv a Y lW 2 dv a rO a p l
  265651. lW -2 dv Y lW 2 dv a p l
  265652. 0 Y p l X Y p l X 0 p l cp f
  265653. 0 0 p M
  265654. 0 Y p l
  265655. X Y p l
  265656. X 0 p l cp
  265657. SM st}{Rr SM st}{rO Y p M rO rO xl
  265658. 0 Y X Y rO ac
  265659. X Y X 0 rO ac
  265660. X 0 0 0 rO ac
  265661. rO neg D xl X Y 0 Y rO ac
  265662. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  265663. -1 -1 sc LB whf}{Asc gs gLB gr
  265664. -0.4 -0.4 sc LB
  265665.  whf}{Asc LB gs whf gr
  265666. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  265667. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  265668. gs 3.6 12 sc gOv gr
  265669. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  265670. gs 3.6 12 sc Cr whf gr
  265671. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  265672. 0 -1 p M
  265673. 0 0 1 0 1 ac
  265674. 8 0 8 1 1 ac
  265675. 8 0 16 0 1 ac
  265676. 16 0 16 -1 1 ac
  265677. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  265678. 2 dv D sc
  265679. 1 0 M -1 0 l
  265680. 0 1 M 0 -1 l
  265681. Ast}{XY 
  265682. D X Y dt 0 0 M SM cpt xl
  265683. 2 dv D sc
  265684. 1 0 M -1 0 l
  265685. Ast}{4.5 Aos
  265686. 1 0 M -1 0 l
  265687. 0 1 M 0 -1 l
  265688. 2 0 M 0 0 2 0 360 arc
  265689. Ast}{4.5 Aos
  265690. 1 0 M -1 0 l
  265691. 2 0 M 0 0 2 0 360 arc
  265692. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  265693. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  265694. 1 -1 M -1 -1 l
  265695. 0 2 M 0 -2 l
  265696. Ast}{5 Aos
  265697. 1 -1 M -1 -1 l
  265698. 1 1 M -1 1 l
  265699. 0 2 M 0 -2 l
  265700. Ast}{4.5 Aos
  265701. 1 0 M -1 0 l
  265702. 0 1 M 0 -1 l
  265703. Ast}{4.5 Aos
  265704. 1 0 M -1 0 l
  265705. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB g
  265706. s whf gr
  265707. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  265708. gs 3.6 12 sc Cr whf gr
  265709. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  265710. gs 3.6 12 sc Cr blf gr
  265711. ZLB whf}{Asc LB gs whf gr
  265712. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  265713. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  265714. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  265715. e 2 ix a}b/PT{D 
  265716. 2 4 gi al P OP D 1 sc
  265717. o length 6 gt{P 6 g}{e P 8 dv}ie
  265718. D lW 2 m lt{P lW 2 m}if
  265719. 0 e p
  265720. 0 0 p
  265721. 3 -1 r s 3 1 r e s e
  265722. 0 0 p M 1 0 p l
  265723. 0 0 p ap M 1 0 p ap l
  265724. e n e n
  265725. 0 0 p ap M 1 0 p ap l
  265726. P P}b/DT{gs np PT SM st gr}b
  265727. O/NH{lW s D hS dv ru
  265728. cvi D 0 eq{P 1}if/nH x
  265729. D hS nH m s
  265730. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  265731. bW 2 dv/bd x
  265732. lW 2 dv e D NH e{D bd p M bd n p l}for
  265733. st gr}{gs 12 OB np
  265734. lW 2 dv 0 xl NH 1 sc
  265735. bW 2 dv wF m nH 1
  265736.  a dv/bd x
  265737. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  265738. np 0 lW 2 dv o o n p M p l bW 2 dv
  265739. wF m o o p l n p l
  265740. cp f gr}{P}{gs 12 OB/bL x
  265741. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  265742. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  265743. bL nSq 2 m dv D sc
  265744. nSq{.135  .667 .865  .667 1 0 rcurveto
  265745. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  265746. np 0 lW 2 dv o o n p M p l bW 2 dv
  265747. wF m o o p l n p l
  265748. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  265749. 1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  265750. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  265751. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  265752. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  265753. 5 -1 r dv neg e 5 -1 r dv neg e
  265754. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  265755. %%EndProcSet
  265756. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  265757. 481 357 195 27 SPn/origstk x
  265758. 65535 65535 65535 sBg
  265759. 0 0 0 C
  265760. 8618 620 M
  265761. 8602 600 l
  265762. 9218 600 l
  265763. 9202 620 l
  265764. 8437 1177 M
  265765. 8413 1185 l
  265766. 8602 600 l
  265767. 8618 620 l
  265768. 8811 1448 M
  265769. 8799 1464 l
  265770. 8413 1185 l
  265771. 8437 1177 l
  265772. 9384 1177 M
  265773. 9396 1181 l
  265774. 9397 1193 l
  265775. 9022 1465 l
  265776. 9010 1449 l
  265777. 9404 1172 M
  265778. 9396 1181 l
  265779. 9384 1177 l
  265780. 9202 620 l
  265781. 9218 600 l
  265782. 861 1269 M
  265783. 9825 1383 l
  265784. 9397 1193 l
  265785. 9396 1181 l
  265786. 9404 1172 l
  265787. 10832 1850 8250 1850 2 Ar
  265788. 5410 5170 5410 2830 2 Ar
  265789. 5600 3564 M
  265790. 5580 3576 l
  265791. 5580 2964 l
  265792. 5600 2976 l
  265793. 5672 3528 M
  265794. 5652 3528 l
  265795. 5652 3012 l
  265796. 5672 3012 l
  265797. 6110 3858 M
  265798. 6110 3882 l
  265799. 5580 3576 l
  265800. 5600 3564 l
  265801. 6620 3564 M
  265802. 6630 3570 l
  265803. 6630 3582 l
  265804. 6110 3882 l
  265805. 6110 3858 l
  265806. 6553 3519 M
  265807. 6563 3537 l
  265808. 6115 3796 l
  265809. 6105 3778 l
  265810. 6620 2976 M
  265811. 6630 2970 l
  265812. 6640 2976 l
  265813. 6640 3564 l
  265814. 6630 3570 l
  265815. 6620 3564 l
  265816. 0 2682 M
  265817. 6110 2658 l
  265818. 6630 2958 l
  265819. 6630 2970 l
  265820. 6620 2976 l
  265821. 6105 2762 M
  265822. 6115 2744 l
  265823. 6563 3003 l
  265824. 6553 3021 l
  265825. 6110 2658 M
  265826. 6110 2682 l
  265827. 5600 2976 l
  265828. 5580 2964 l
  265829. 7045 3798 M
  265830. 7035 3816 l
  265831. 6630 3582 l
  265832. 6630 3570 l
  265833. 6640 3564 l
  265834. 7043 2719 M
  265835. 7053 2737 l
  265836. 6640 2976 l
  265837. 6630 2970 l
  265838. 6630 2958 l
  265839. 5570 1398 M
  265840. 5570 1422 l
  265841. 5150 1665 l
  265842. 5140 1647 l
  265843. 5985 1638 M
  265844. 5975 1656 l
  265845. 5570 1422 l
  265846. 5570 1398 l
  265847. 5524 930 M
  265848. 5544 930 l
  265849. 5544 1430 l
  265850. 5524 1430 l
  265851. 5596 930 M
  265852.  930 l
  265853. 5616 1430 l
  265854. 5596 1430 l
  265855. 4810 6138 M
  265856. 4810 6162 l
  265857. 4375 6413 l
  265858. 4365 6395 l
  265859. 5225 6378 M
  265860. 5215 6396 l
  265861. 4810 6162 l
  265862. 4810 6138 l
  265863. 4764 5680 M
  265864. 4784 5680 l
  265865. 4784 6170 l
  265866. 4764 6170 l
  265867. 4836 5680 M
  265868. 4856 5680 l
  265869. 4856 6170 l
  265870. 4836 6170 l
  265871. 5840 6144 M
  265872. 5850 6150 l
  265873. 5850 6162 l
  265874. 5445 6396 l
  265875. 5435 6378 l
  265876. 6370 6440 M
  265877. 6370 6452 l
  265878. 6360 6458 l
  265879. 5850 6162 l
  265880. 5850 6150 l
  265881. 5860 6144 l
  265882. 6375 6360 M
  265883. 6365 6378 l
  265884. 5917 6117 l
  265885. 5927 6099 l
  265886. 6882 6144 M
  265887. 6902 6156 l
  265888. 0 6458 l
  265889. 6370 6452 l
  265890. 6370 6440 l
  265891. 6882 5555 M
  265892. 6902 5543 l
  265893. 6902 6156 l
  265894. 6882 6144 l
  265895. 6810 5591 M
  265896. 6830 5591 l
  265897. 6830 6108 l
  265898. 6810 6108 l
  265899. 6370 5259 M
  265900. 6370 5235 l
  265901. 6902 5543 l
  265902. 6882 5555 l
  265903. 5860 5555 M
  265904. 5840 5543 l
  265905. 6370 5235 l
  265906. 6370 5259 l
  265907. 5927 5600 M
  265908. 5917 5582 l
  265909. 6365 5321 l
  265910. 6375 5339 l
  265911. 5840 5543 M
  265912. 5860 5555 l
  265913. 5860 6144 l
  265914. 5850 6150 l
  265915. 5840 6144 l
  265916. 6380 6940 M
  265917. 6360 6940 l
  265918. 6360 6458 l
  265919. 6370 6452 l
  265920. 6380 6458 l
  265921. 11920 1448 M
  265922. 11920 1472 l
  265923. 11482 1725 
  265924. 11472 1707 l
  265925. 12355 1699 M
  265926. 12345 1717 l
  265927. 11920 1472 l
  265928. 11920 1448 l
  265929. 11874 980 M
  265930. 11894 980 l
  265931. 11894 1480 l
  265932. 11874 1480 l
  265933. 11946 980 M
  265934. 11966 980 l
  265935. 11966 1480 l
  265936. 11946 1480 l
  265937. 12603 2330 M
  265938. 12595 2340 l
  265939. 12584 2337 l
  265940. 12463 1886 l
  265941. 12483 1880 l
  265942. 13188 2362 M
  265943. 13202 2382 l
  265944. 12600 2350 l
  265945. 12595 2340 l
  265946. 12603 2330 l
  265947. 13398 1814 M
  265948. 13422 1808 l
  265949. 13202 2382 l
  265950. 13188 2362 l
  265951. 12941 1446 M
  265952. 12943 1422 l
  265953. 13422 1808 l
  265954. 13398 1814 l
  265955. 12943 1422 M
  265956. 12941 1446 l
  265957. 34 1710 l
  265958. 12524 1694 l
  265959. 12326 2767 M
  265960. 12232 2691 l
  265961. 12584 2337 l
  265962. 12595 2340 l
  265963. 12600 2350 l
  265964. count origstk sub{P}rp end
  265965. chemsave restore
  265966.     Helvetica
  265967. Times
  265968. C, 20min
  265969. RT, 2h
  265970. BocHN
  265971. NHBoc
  265972. 2) CF
  265973. 2) CF
  265974. tCHMD
  265975. S    .1=
  265976. CO2Bn
  265977. NHBoc<
  265978. NHBoc
  265979. CO2Bn
  265980. HgCl2
  265981. HgCl2
  265982. 0oC, 20min
  265983. RT, 2h
  265984. 2) CF3COOH
  265985. 2) CF3COOH
  265986.     Helvetica
  265987. Times
  265988. 0swsD
  265989.     Helvetica
  265990.     Helvetica
  265991.     Helvetica
  265992. CO2Bn
  265993. HgCl2
  265994.     Helvetica
  265995.     Helvetica
  265996. HgCl2
  265997. 0oC, 20min
  265998. RT, 2h
  265999.     Helvetica
  266000. BocHN^<
  266001. NHBoc6
  266002.     Helvetica
  266003. NHBoc<
  266004. NHBoc6
  266005.     Helvetica
  266006. 2) CF3COOH
  266007. 2) CF3COOH
  266008.     Helvetica
  266009.     Helvetica
  266010.     Helvetica
  266011.     Helvetica
  266012.     Helvetica
  266013.     Helvetica
  266014.     Helvetica
  266015.     Helvetica
  266016. BnO2C^
  266017. Untitled Refs-3
  266018. count
  266019. currentpoint 192837465
  266020. currentpoint
  266021. save/chemsave exch def
  266022. %%BeginProcSet: chemdict30 24 10
  266023. % ChemDraw Laser Prep
  266024. % Copyright 1986-1995
  266025. , CambridgeSoft Corporation
  266026. userdict/chemdict30 210 dict put
  266027. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/rm/
  266028. rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d/cW 
  266029. 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  266030. x}b/sRmp{current
  266031. rgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  266032. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  266033. 0 cw 2 dv xl
  266034. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  266035. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  266036. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  266037. St 16 and 0 ne{2 ix 6 m 1 a 
  266038. D ix e D ix e D ix e D ix e P SpA}if
  266039. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  266040. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  266041. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  266042. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  266043. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  266044. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc cp 
  266045. f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  266046. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  266047. P P}{sq at 2
  266048. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  266049. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  266050. l w .35 dv w -2 
  266051. m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  266052. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  266053. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  266054. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  266055. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  266056. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1 s
  266057. c 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  266058. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  266059. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  266060. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  266061. 21 -10 27 -8 27 0 cv
  266062. 27 8 21 10 9 6 cv
  266063. -3 2 -3 -2 9 -6 cv
  266064. cp}b/DLB{0 0 M -4.8 4.8 l
  266065. -8 8 -9.6 12 -9.6 16.8 cv
  266066. -9.6 21.6 -8 24.6 
  266067. -4.8 25.8 cv
  266068. -1.6 27 1.6 27 4.8 25.8 cv
  266069. 8 24.6 9.6 21.6 9.6 16.8 cv
  266070. 9.6 12 8 8 4.8 4.8 cv
  266071. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  266072. 0 Y X Y rO ac
  266073. X Y X 0 rO ac
  266074. X 0 0 0 rO ac
  266075. 0 0 0 Y rO ac
  266076. cp}b/Rc{0 0 p M
  266077. 0 Y p l
  266078. X Y p l
  266079. X 0 p l
  266080. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  266081. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  266082.  D 0 lt{n}if sq n D
  266083. CMT dtransform idtransform
  266084. e 2 m e
  266085. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  266086. 32 -0.5 0.5{gs
  266087. 13.5 0 xl
  266088. D 32 s 64 dv 13.5 m D 7 m 24 dv
  266089. -13.5 0 xl
  266090. gr}for
  266091. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  266092. 32 -0.5 0.5{gs
  266093. D 32 s 64 dv 0.65 m D
  266094. gr}for
  266095. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  266096. 32 -0.5 0.5{gs
  266097. D 32 s 64 dv D
  266098. gr}for
  266099. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  266100. 32 -0.5 0.5{gs
  266101. 0 13.5 xl
  266102. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  266103. 0 -13.5 xl
  266104. DLB f
  266105. gr}for
  266106. DLB SM st}{DLB grf}i
  266107. e}b/gRr{sh{sRmp
  266108. 32 -0.5 0.5{gs
  266109. X 2 dv Y 2 dv xl
  266110. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  266111. X -2 dv Y -2 dv xl
  266112. gr}for
  266113. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  266114. 32 -0.5 0.5{gs
  266115. X 2 dv Y 2 dv xl
  266116. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  266117. X -2 dv Y -2 dv xl
  266118. gr}for
  266119. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  266120. rev{1 -1 sc}if
  266121. 0 lW 2 m xl
  266122. D SA OA
  266123. rad 0 xl
  266124. 180 ro
  266125. 0 lW 2 m xl
  266126. SA OA}b/Aos{X Y M SM cpt xl XY e 
  266127. dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  266128. o 0 lt o 0 lt ne/rev x
  266129. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  266130. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  266131. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  266132. lp 0 p M
  266133. 0 0 0 Y lp ac
  266134. 0 Y 2 dv lp neg o lp ac
  266135. 0 Y 2 dv 0 Y lp ac
  266136. 0 Y lp Y lp ac
  266137. X lp s 0 p M
  266138. X 0 X Y lp ac
  266139. X Y 2 dv X lp a o lp ac
  266140. X Y 2 dv X Y lp ac
  266141. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA a
  266142.  arc st
  266143. np X Y s Y 2 dv
  266144. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  266145. rO D rlineto
  266146. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  266147. rO lW -2 dv a Y lW 2 dv a rO a p l
  266148. lW -2 dv Y lW 2 dv a p l
  266149. 0 Y p l X Y p l X 0 p l cp f
  266150. 0 0 p M
  266151. 0 Y p l
  266152. X Y p l
  266153. X 0 p l cp
  266154. SM st}{Rr SM st}{rO Y p M rO rO xl
  266155. 0 Y X Y rO ac
  266156. X Y X 0 rO ac
  266157. X 0 0 0 rO ac
  266158. rO neg D xl X Y 0 Y rO ac
  266159. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  266160. -1 -1 sc LB whf}{Asc gs gLB gr
  266161. -0.4 -0.4 sc LB whf
  266162. }{Asc LB gs whf gr
  266163. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  266164. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  266165. gs 3.6 12 sc gOv gr
  266166. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  266167. gs 3.6 12 sc Cr whf gr
  266168. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  266169. 0 -1 p M
  266170. 0 0 1 0 1 ac
  266171. 8 0 8 1 1 ac
  266172. 8 0 16 0 1 ac
  266173. 16 0 16 -1 1 ac
  266174. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  266175. 2 dv D sc
  266176. 1 0 M -1 0 l
  266177. 0 1 M 0 -1 l
  266178. Ast}{XY D X 
  266179. Y dt 0 0 M SM cpt xl
  266180. 2 dv D sc
  266181. 1 0 M -1 0 l
  266182. Ast}{4.5 Aos
  266183. 1 0 M -1 0 l
  266184. 0 1 M 0 -1 l
  266185. 2 0 M 0 0 2 0 360 arc
  266186. Ast}{4.5 Aos
  266187. 1 0 M -1 0 l
  266188. 2 0 M 0 0 2 0 360 arc
  266189. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  266190. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  266191. 1 -1 M -1 -1 l
  266192. 0 2 M 0 -2 l
  266193. Ast}{5 Aos
  266194. 1 -1 M -1 -1 l
  266195. 1 1 M -1 1 l
  266196. 0 2 M 0 -2 l
  266197. Ast}{4.5 Aos
  266198. 1 0 M -1 0 l
  266199. 0 1 M 0 -1 l
  266200. Ast}{4.5 Aos
  266201. 1 0 M -1 0 l
  266202. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs wh
  266203. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  266204. gs 3.6 12 sc Cr whf gr
  266205. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  266206. gs 3.6 12 sc Cr blf gr
  266207. ZLB whf}{Asc LB gs whf gr
  266208. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  266209. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  266210. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  266211. e 2 ix a}b/PT{D 2 4 
  266212. gi al P OP D 1 sc
  266213. o length 6 gt{P 6 g}{e P 8 dv}ie
  266214. D lW 2 m lt{P lW 2 m}if
  266215. 0 e p
  266216. 0 0 p
  266217. 3 -1 r s 3 1 r e s e
  266218. 0 0 p M 1 0 p l
  266219. 0 0 p ap M 1 0 p ap l
  266220. e n e n
  266221. 0 0 p ap M 1 0 p ap l
  266222. P P}b/DT{gs np PT SM st gr}b
  266223. O/NH{lW s D hS dv ru
  266224. cvi D 0 eq{P 1}if/nH x
  266225. D hS nH m s
  266226. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  266227. bW 2 dv/bd x
  266228. lW 2 dv e D NH e{D bd p M bd n p l}for
  266229. st gr}{gs 12 OB np
  266230. lW 2 dv 0 xl NH 1 sc
  266231. bW 2 dv wF m nH 1 a d
  266232. v/bd x
  266233. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  266234. np 0 lW 2 dv o o n p M p l bW 2 dv
  266235. wF m o o p l n p l
  266236. cp f gr}{P}{gs 12 OB/bL x
  266237. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  266238. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  266239. bL nSq 2 m dv D sc
  266240. nSq{.135  .667 .865  .667 1 0 rcurveto
  266241. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  266242. np 0 lW 2 dv o o n p M p l bW 2 dv
  266243. wF m o o p l n p l
  266244. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  266245. 5 -1 r 
  266246. xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  266247. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  266248. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  266249. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  266250. 5 -1 r dv neg e 5 -1 r dv neg e
  266251. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  266252. %%EndProcSet
  266253. 40 80 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  266254. 706 267 5 44 SPn/origstk x
  266255. 65535 65535 65535 sBg
  266256. 0 0 0 C
  266257. 4750 1904 M
  266258. 4730 1916 l
  266259. 4730 1304 l
  266260. 4750 1316 l
  266261. 4822 1868 M
  266262. 4802 1868 l
  266263. 4802 1352 l
  266264. 4822 1352 l
  266265. 5260 2198 M
  266266. 5260 2222 l
  266267. 4730 1916 l
  266268. 4750 1904 l
  266269. 5770 1904 M
  266270. 5780 1910 l
  266271. 5781 1921 l
  266272. 5260 2222 l
  266273. 5260 2198 l
  266274. 5703 1859 M
  266275. 5713 1877 l
  266276. 5265 2136 l
  266277. 5255 2118 l
  266278. 5770 1316 M
  266279. 5780 1310 l
  266280. 5790 1318 l
  266281. 5790 1902 l
  266282. 5780 1910 l
  266283. 5770 1904 l
  266284. 5260 1022 M
  266285. 5260 998 l
  266286. 5781 1299 l
  266287. 5780 1310 l
  266288. 5770 1316 l
  266289. 5255 1102 M
  266290. 5265 1084 l
  266291. 5713 1343 l
  266292. 5703 1361 l
  266293. 5260 998 M
  266294. 5260 1022 l
  266295. 4750 1316 l
  266296. 4730 1304 l
  266297. 6347 2083 M
  266298. 6351 2095 l
  266299. 6343 2103 l
  266300. 5781 1921 l
  266301. 5780 1910 l
  266302. 5790 1902 l
  266303. 6691 1609 M
  266304. 6715 1609 l
  266305. 6362 2096 l
  266306. 6351 2095 l
  266307. 6347 2083 l
  266308. 6606 1603 M
  266309. 6622 1615 l
  266310. 6331 2016 l
  266311. 6315 2004 l
  266312. 6414 1228 M
  266313. 6430 1216 l
  266314. 6715 1609 l
  266315. 6691 1609 l
  266316. 6211 1158 M
  266317. 6217 1178 l
  266318. 5790 1318 l
  266319. 5780 1310 l
  266320. 5781 1299 l
  266321. 6545 2655 M
  266322. 6529 2675 l
  266323. 6343 2103 l
  266324. 6351 2095 l
  266325. 6362 2096 l
  266326. 7133 2655 M
  266327. 7141 2675 l
  266328. 6529 2675 l
  266329. 6545 2655 l
  266330. 7453 2335 M
  266331. 7467 2349 l
  266332. 7141 2675 l
  266333. 7133 2655 l
  266334. 7395 1658 M
  266335. 7417 1664 l
  266336. 7537 2109 l
  266337. 7517 2115 l
  266338. 7735 1318 M
  266339. 7749 1332 l
  266340. 7417 1664 l
  266341. 7395 1658 l
  266342. 7786 1369 M
  266343. 7800 1383 l
  266344. 7493 1690 l
  266345. 7479 1676 l
  266346. 8640 2824 M
  266347. 8620 2836 l
  266348. 8620 2224 l
  266349. 8640 2236 l
  266350. 8712 2788 M
  266351. 8692 2788 l
  266352. 8692 2272 l
  266353. 8712 2272 l
  266354. 150 3118 M
  266355. 9150 3142 l
  266356. 8620 2836 l
  266357. 8640 2824 l
  266358. 9660 2824 M
  266359. 9670 2830 l
  266360. 9671 2841 l
  266361. 9150 3142 l
  266362. 9150 3118 l
  266363. 9593 2779 M
  266364. 9603 2797 l
  266365. 9155 3056 l
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  266367. 9660 2236 M
  266368. 9670 2230 l
  266369. 9680 2238 l
  266370. 9680 2822 l
  266371. 9670 2830 l
  266372. 9660 2824 l
  266373. 9150 1942 M
  266374. 9150 1918 l
  266375. 9671 2219 l
  266376. 9670 2230 l
  266377. 9660 2236 l
  266378. 9145 2022 M
  266379. 9155 2004 l
  266380. 9603 2263 l
  266381. 9593 2281 l
  266382. 9150 1918 M
  266383. 9150 1942 l
  266384. 8640 2236 l
  266385. 8620 2224 l
  266386. 10237 3003 M
  266387. 10241 3015 l
  266388. 10233 3023 l
  266389. 9671 2841 l
  266390.  2830 l
  266391. 9680 2822 l
  266392. 10581 2529 M
  266393. 10605 2529 l
  266394. 10252 3016 l
  266395. 10241 3015 l
  266396. 10237 3003 l
  266397. 10496 2523 M
  266398. 10512 2535 l
  266399. 10221 2936 l
  266400. 10205 2924 l
  266401. 10308 2153 M
  266402. 10324 2141 l
  266403. 10605 2529 l
  266404. 10581 2529 l
  266405. 10110 2075 M
  266406. 10116 2095 l
  266407. 9680 2238 l
  266408. 9670 2230 l
  266409. 9671 2219 l
  266410. 10435 3575 M
  266411. 10419 3595 l
  266412. 10233 3023 l
  266413. 10241 3015 l
  266414. 10252 3016 l
  266415. 11023 3575 M
  266416. 11031 3595 l
  266417. 10419 3595 l
  266418. 10435 3575 l
  266419. 11348 3250 M
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  266421. 11031 3595 l
  266422. 11023 3575 l
  266423. 11285 2578
  266424. 11307 2584 l
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  266426. 11407 3037 l
  266427. 11710 2153 M
  266428. 11732 2159 l
  266429. 11307 2584 l
  266430. 11285 2578 l
  266431. 11634 2127 M
  266432. 11648 2141 l
  266433. 11252 2537 l
  266434. 11238 2523 l
  266435. 11585 1689 M
  266436. 11605 1683 l
  266437. 11732 2159 l
  266438. 11710 2153 l
  266439. 370 5324 M
  266440. 350 5336 l
  266441. 350 4724 l
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  266443. 442 5288 M
  266444. 422 5288 l
  266445. 422 4772 l
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  266447. 880 5618 M
  266448. 880 5642 l
  266449. 350 5336 l
  266450. 370 5324 l
  266451. 1390 5324 M
  266452. 1400 5330 l
  266453. 1401 5341 l
  266454. 880 5642 l
  266455. 880 5618 l
  266456. 1323 5279 M
  266457. 1333 5297 l
  266458. 885 5556 l
  266459. 875 553
  266460. 1390 4736 M
  266461. 1400 4730 l
  266462. 1410 4738 l
  266463. 1410 5322 l
  266464. 1400 5330 l
  266465. 1390 5324 l
  266466. 880 4442 M
  266467. 880 4418 l
  266468. 1401 4719 l
  266469. 1400 4730 l
  266470. 1390 4736 l
  266471. 875 4522 M
  266472. 885 4504 l
  266473. 1333 4763 l
  266474. 1323 4781 l
  266475. 880 4418 M
  266476. 880 4442 l
  266477. 370 4736 l
  266478. 350 4724 l
  266479. 1967 5503 M
  266480. 1971 5515 l
  266481. 1964 5524 l
  266482. 1401 5341 l
  266483. 1400 5330 l
  266484. 1410 5322 l
  266485. 2311 5029 M
  266486. 2323 5029 l
  266487. 2328 5040 l
  266488. 1982 5516 l
  266489. 1971 5515 l
  266490. 1967 5503 l
  266491. 2226 5023 M
  266492. 2242 5035 l
  266493. 1951 5436 l
  266494. 1935 5424 l
  266495. 2034 4648 M
  266496. 50 4636 l
  266497. 2328 5019 l
  266498. 2323 5029 l
  266499. 2311 5029 l
  266500. 1831 4578 M
  266501. 1837 4598 l
  266502. 1410 4738 l
  266503. 1400 4730 l
  266504. 1401 4719 l
  266505. 2223 6054 M
  266506. 2209 6072 l
  266507. 1964 5524 l
  266508. 1971 5515 l
  266509. 1982 5516 l
  266510. 2809 6114 M
  266511. 2819 6136 l
  266512. 2209 6072 l
  266513. 2223 6054 l
  266514. 3072 5752 M
  266515. 3088 5764 l
  266516. 2819 6136 l
  266517. 2809 6114 l
  266518. 2915 5098 M
  266519. 2922 5089 l
  266520. 2933 5090 l
  266521. 3120 5507 l
  266522. 3102 5515 l
  266523. 2917 5078 M
  266524. 2922 5089 l
  266525. 2915 5098 l
  266526. 2328 5040 l
  266527. 2323 5029 l
  266528. 2328 5019 l
  266529. 3262 4602 M
  266530. 3284 4604 l
  266531. 2933 5090 l
  266532. 2922 508
  266533. 2917 5078 l
  266534. 3061 4157 M
  266535. 3079 4149 l
  266536. 3284 4604 l
  266537. 3262 4602 l
  266538. 3240 2630 1840 2630 2 Ar
  266539. 3890 2490 M
  266540. 3870 2490 l
  266541. 3870 1890 l
  266542. t3890 1890 l
  266543. 8200 2730 5040 2730 2 Ar
  266544. 14160 2665 12300 2665 2 Ar
  266545. count origstk sub{P}rp end
  266546. chemsave restore
  266547.     Helvetica
  266548. Times
  266549. ArCHSiMe
  266550. ArCHSiMe
  266551. LDA,  THF
  266552. C --> r.t.
  266553. C  -->  r.t.
  266554. MeOH - HCl
  266555.  CHMD
  266556.  ArCHSiMe3
  266557.  ArCHSiMe3
  266558. LDA,  THF
  266559. -25oC --> r.t.
  266560. -60oC  -->  r.t.
  266561.     81$    
  266562. MeOH - HCl
  266563.     Helvetica
  266564. Times
  266565. nswsD
  266566.     Helvetica
  266567. lvetica
  266568.     Helvetica
  266569.     Helvetica
  266570.     Helvetica
  266571.     Helvetica
  266572.     Helvetica
  266573.     Helvetica
  266574.     Helvetica
  266575.     Helvetica
  266576.  ArCHSiMe3
  266577.  ArCHSiMe3
  266578. LDA,  THF
  266579. -25oC --> r.t.
  266580. -60oC  -->  r.t.
  266581.     81$    
  266582.     81$    
  266583. MeOH - HCl
  266584. Untitled preferences-1
  266585. count
  266586. currentpoint 192837465
  266587. currentpoint
  266588. save/chemsave exch def
  266589. %%BeginProcSet: chemdict30 24 10
  266590. % ChemDraw Laser Prep
  266591. % Copyright 198
  266592. , CambridgeSoft Corporation
  266593. userdict/chemdict30 210 dict put
  266594. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop L/r/roll L/rm/
  266595. rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/cpd R/sf 20 d/cW 
  266596. 20 d/lW 20 d/bW 75 d/wF 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  266597. x}b/sRmp{current
  266598. rgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  266599. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  266600. 0 cw 2 dv xl
  266601. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  266602. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  266603. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  266604. St 16 and 0 ne{2 ix 6 m 1 a 
  266605. D ix e D ix e D ix e D ix e P SpA}if
  266606. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  266607. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  266608. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  266609. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  266610. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  266611. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA a arc cp 
  266612. f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  266613. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  266614. P P}{sq at 2
  266615. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  266616. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  266617. l w .35 dv w -2 
  266618. m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  266619. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  266620. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5
  266621. HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  266622. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA
  266623. OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA OA}{1 -1 s
  266624. c 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  266625. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270
  266626. AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  266627. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  266628. 21 -10 27 -8 27 0 cv
  266629. 27 8 21 10 9 6 cv
  266630. -3 2 -3 -2 9 -6 cv
  266631. cp}b/DLB{0 0 M -4.8 4.8 l
  266632. -8 8 -9.6 12 -9.6 16.8 cv
  266633. -9.6 21.6 -8 24.6 
  266634. -4.8 25.8 cv
  266635. -1.6 27 1.6 27 4.8 25.8 cv
  266636. 8 24.6 9.6 21.6 9.6 16.8 cv
  266637. 9.6 12 8 8 4.8 4.8 cv
  266638. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  266639. 0 Y X Y rO ac
  266640. X Y X 0 rO ac
  266641. X 0 0 0 rO ac
  266642. 0 0 0 Y rO ac
  266643. cp}b/Rc{0 0 p M
  266644. 0 Y p l
  266645. X Y p l
  266646. X 0 p l
  266647. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  266648. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idtransform
  266649.  D 0 lt{n}if sq n D
  266650. CMT dtransform idtransform
  266651. e 2 m e
  266652. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  266653. 32 -0.5 0.5{gs
  266654. 13.5 0 xl
  266655. D 32 s 64 dv 13.5 m D 7 m 24 dv
  266656. -13.5 0 xl
  266657. gr}for
  266658. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  266659. 32 -0.5 0.5{gs
  266660. D 32 s 64 dv 0.65 m D
  266661. gr}for
  266662. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  266663. 32 -0.5 0.5{gs
  266664. D 32 s 64 dv D
  266665. gr}for
  266666. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  266667. 32 -0.5 0.5{gs
  266668. 0 13.5 xl
  266669. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  266670. 0 -13.5 xl
  266671. DLB f
  266672. gr}for
  266673. DLB SM st}{DLB grf}i
  266674. e}b/gRr{sh{sRmp
  266675. 32 -0.5 0.5{gs
  266676. X 2 dv Y 2 dv xl
  266677. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  266678. X -2 dv Y -2 dv xl
  266679. gr}for
  266680. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  266681. 32 -0.5 0.5{gs
  266682. X 2 dv Y 2 dv xl
  266683. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  266684. X -2 dv Y -2 dv xl
  266685. gr}for
  266686. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  266687. rev{1 -1 sc}if
  266688. 0 lW 2 m xl
  266689. D SA OA
  266690. rad 0 xl
  266691. 180 ro
  266692. 0 lW 2 m xl
  266693. SA OA}b/Aos{X Y M SM cpt xl XY e 
  266694. dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  266695. o 0 lt o 0 lt ne/rev x
  266696. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  266697. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  266698. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  266699. lp 0 p M
  266700. 0 0 0 Y lp ac
  266701. 0 Y 2 dv lp neg o lp ac
  266702. 0 Y 2 dv 0 Y lp ac
  266703. 0 Y lp Y lp ac
  266704. X lp s 0 p M
  266705. X 0 X Y lp ac
  266706. X Y 2 dv X lp a o lp ac
  266707. X Y 2 dv X Y lp ac
  266708. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA s 180 pA a
  266709.  arc st
  266710. np X Y s Y 2 dv
  266711. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  266712. rO D rlineto
  266713. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  266714. rO lW -2 dv a Y lW 2 dv a rO a p l
  266715. lW -2 dv Y lW 2 dv a p l
  266716. 0 Y p l X Y p l X 0 p l cp f
  266717. 0 0 p M
  266718. 0 Y p l
  266719. X Y p l
  266720. X 0 p l cp
  266721. SM st}{Rr SM st}{rO Y p M rO rO xl
  266722. 0 Y X Y rO ac
  266723. X Y X 0 rO ac
  266724. X 0 0 0 rO ac
  266725. rO neg D xl X Y 0 Y rO ac
  266726. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  266727. -1 -1 sc LB whf}{Asc gs gLB gr
  266728. -0.4 -0.4 sc LB whf
  266729. }{Asc LB gs whf gr
  266730. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  266731. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  266732. gs 3.6 12 sc gOv gr
  266733. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  266734. gs 3.6 12 sc Cr whf gr
  266735. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  266736. 0 -1 p M
  266737. 0 0 1 0 1 ac
  266738. 8 0 8 1 1 ac
  266739. 8 0 16 0 1 ac
  266740. 16 0 16 -1 1 ac
  266741. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  266742. 2 dv D sc
  266743. 1 0 M -1 0 l
  266744. 0 1 M 0 -1 l
  266745. Ast}{XY D X 
  266746. Y dt 0 0 M SM cpt xl
  266747. 2 dv D sc
  266748. 1 0 M -1 0 l
  266749. Ast}{4.5 Aos
  266750. 1 0 M -1 0 l
  266751. 0 1 M 0 -1 l
  266752. 2 0 M 0 0 2 0 360 arc
  266753. Ast}{4.5 Aos
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  266760. Ast}{5 Aos
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  266764. Ast}{4.5 Aos
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  266766. 0 1 M 0 -1 l
  266767. Ast}{4.5 Aos
  266768. 1 0 M -1 0 l
  266769. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc DLB gs wh
  266770. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  266771. gs 3.6 12 sc Cr whf gr
  266772. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  266773. gs 3.6 12 sc Cr blf gr
  266774. ZLB whf}{Asc LB gs whf gr
  266775. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  266776. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  266777. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  266778. e 2 ix a}b/PT{D 2 4 
  266779. gi al P OP D 1 sc
  266780. o length 6 gt{P 6 g}{e P 8 dv}ie
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  266790. O/NH{lW s D hS dv ru
  266791. cvi D 0 eq{P 1}if/nH x
  266792. D hS nH m s
  266793. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  266794. bW 2 dv/bd x
  266795. lW 2 dv e D NH e{D bd p M bd n p l}for
  266796. st gr}{gs 12 OB np
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  266800. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  266801. np 0 lW 2 dv o o n p M p l bW 2 dv
  266802. wF m o o p l n p l
  266803. cp f gr}{P}{gs 12 OB/bL x
  266804. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  266805. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  266806. bL nSq 2 m dv D sc
  266807. nSq{.135  .667 .865  .667 1 0 rcurveto
  266808. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  266809. np 0 lW 2 dv o o n p M p l bW 2 dv
  266810. wF m o o p l n p l
  266811. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al P
  266812. 5 -1 r 
  266813. xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  266814. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  266815. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  266816. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  266817. 5 -1 r dv neg e 5 -1 r dv neg e
  266818. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  266819. %%EndProcSet
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  267262. 65535 65535 65535 C
  267263. 3540 5319 M
  267264. 1 5291 l
  267265. 3573 5207 l
  267266. 3462 5234 l
  267267. 3832 5184 M
  267268. 3842 5202 l
  267269. 3267 5345 l
  267270. 3255 5338 l
  267271. 3260 5326 l
  267272. 3842 5202 M
  267273. 3832 5184 l
  267274. 4273 4663 l
  267275. 4285 4664 l
  267276. 4275 4692 l
  267277. 3373 5914 M
  267278. 3385 5921 l
  267279. 3381 5933 l
  267280. 2820 6108 l
  267281. 2810 6100 l
  267282. 2811 6089 l
  267283. 6230 6804 M
  267284. 6210 6816 l
  267285. 6210 6204 l
  267286. 6230 6216 l
  267287. 6302 6768 M
  267288. 6282 6768 l
  267289. 6282 6252 l
  267290. 6302 6252 l
  267291. 6740 7098 M
  267292. 6740 7122 l
  267293. 6210 6816 l
  267294. 6230 6804 l
  267295. 7250 6804 M
  267296. 7260 6810 l
  267297. 7261 6821 l
  267298. 6740 7122 l
  267299. 6740 7098 l
  267300. 7183 6759 M
  267301. 7193 6777 l
  267302. 6745 7036 l
  267303. 6735 7018 l
  267304. 7250 6216 M
  267305. 7260 6210 l
  267306. 7270 6218 l
  267307. 7270 6802 l
  267308. 7260 6810 l
  267309. 7250 6804 l
  267310. 6740 5922 M
  267311. 6740 5910 l
  267312. 6750 5904 l
  267313. 7261 6199 l
  267314. 7260 6210 l
  267315. 7250 6216 l
  267316. 6735 6002 M
  267317. 6745 5984 l
  267318. 7193 6243 l
  267319. 7183 6261 l
  267320. 6730 5904 M
  267321. 6740 5910 l
  267322. 6740 5922 l
  267323. 6230 6216 l
  267324. 6210 6204 l
  267325. 7716 6947 M
  267326. 7710 6967 l
  267327. 7261 6821 l
  267328. 7260 6810 l
  267329. 7270 6802 l
  267330. 8171 6509 M
  267331. 8195 6509 l
  267332. 7916 6894 l
  267333. 7900 6882 l
  267334. 8670 6463 M
  267335. 8670 6483 l
  267336. 7 6483 l
  267337. 8157 6463 l
  267338. 8670 6535 M
  267339. 8670 6555 l
  267340. 8157 6555 l
  267341. 8157 6535 l
  267342. 6730 5430 M
  267343. 6750 5430 l
  267344. 6750 5904 l
  267345. 6740 5910 l
  267346. 6730 5904 l
  267347. 7746 5076 M
  267348. 7726 5084 l
  267349. 7758 4366 l
  267350. 7770 4327 l
  267351. 7780 4335 l
  267352. 7435 4897 M
  267353. 7411 4897 l
  267354. 7763 4318 l
  267355. 7770 4327 l
  267356. 7758 4366 l
  267357. 7726 5084 M
  267358. 7746 5076 l
  267359. 8145 5508 l
  267360. 8142 5519 l
  267361. 8129 5520 l
  267362. 8129 5520 M
  267363. 8142 5519 l
  267364. 8149 5528 l
  267365. 7847 6031 l
  267366. 7835 6031 l
  267367. 7839 6004 l
  267368. 7695 5450 M
  267369. 7705 5448 l
  267370. 7717 5455 l
  267371. 7839 6004 l
  267372. 7835 6031
  267373. 7823 6024 l
  267374. 7710 5436 M
  267375. 7705 5448 l
  267376. 7696 5453 l
  267377. 7411 4897 l
  267378. 7435 4897 l
  267379. 8715 5366 M
  267380. 8735 5382 l
  267381. 8149 5528 l
  267382. 8142 5519 l
  267383. 8145 5508 l
  267384. 8356 4171 M
  267385. 8348 4193 l
  267386. 7780 4335 l
  267387. 7770 4327 l
  267388. 7763 4318 l
  267389. 8725 4802 M
  267390. 8735 4774 l
  267391. 8745 4772 l
  267392. 8735 5382 l
  267393. 8715 5366 l
  267394. 8745 4772 M
  267395. 8735 4774 l
  267396. 8723 4773 l
  267397. 8348 4193 l
  267398. 8356 4171 l
  267399. 65535 65535 65535 C
  267400. 7990 5429 M
  267401. 8101 5401 l
  267402. 8023 5317 l
  267403. 7912 5344 l
  267404. 8282 5294 M
  267405. 8292 5312 l
  267406. 7717 5455 l
  267407. 7705 5448 l
  267408. 7710 5436 l
  267409. 8292 5312 M
  267410. 8282 5294 l
  267411. 8723 4773 l
  267412. 8735 4774 l
  267413. 8725 4802 l
  267414. 7823 6024 M
  267415. 7835 6031 l
  267416. 7831 6043 l
  267417. 7270 6218 l
  267418. 7260 6210 l
  267419. 7261 6199 l
  267420. 3381 5933 M
  267421. 3385 5921 l
  267422. 3397 5921 l
  267423. 3738 6389 l
  267424. 3733 6399 l
  267425. 3721 6399 l
  267426. 7831 6043 M
  267427. 7835 6031 l
  267428. 7847 6031 l
  267429. 8195 6509 l
  267430. 8171 6509 l
  267431. 5984 5449 4550 5449 2 Ar
  267432. count origstk sub{P}rp end
  267433. chemsave restore
  267434.     Helvetica
  267435. Times
  267436. LDA  /  TMSCl
  267437. Adamantone
  267438.     TFA  /  H
  267439.     O  (2:1)
  267440. 6hr    85%
  267441. hv  2hr
  267442. SiMe3(
  267443. SiMe3-
  267444. SiMe3
  267445. SiMe30
  267446. LDA  /  TMSClO
  267447. -78oCT
  267448. Adamantone
  267449.     R,X    
  267450. TFA  /  H2O  (2:1)
  267451. 6hr    85%
  267452. hv  2hr
  267453.     Helvetica
  267454. Times
  267455. JswsD
  267456.     Helvetica
  267457.     Helvetica
  267458.     Helvetica
  267459.     Helvetica
  267460.     Helvetica
  267461. MeO^<
  267462. LDA  /  TMSCl
  267463. -78oC
  267464.     Helvetica
  267465.     Helvetica
  267466.     Helvetica
  267467.     Helvetica
  267468. MeO^<
  267469.     Helvetica
  267470. SiMe3<
  267471. SiMe36
  267472.     Helvetica
  267473. SiMe3<
  267474. SiMe36
  267475.     Helvetica
  267476. SiMe3<
  267477. SiMe36
  267478. Adamantone
  267479.     Helvetica
  267480.     Helvetica
  267481.     Helvetica
  267482.     Helvetica
  267483. MeO^<
  267484.     Helvetica
  267485. SiMe3<
  267486. SiMe36
  267487.     Helvetica
  267488.     Helvetica
  267489.     Helvetica
  267490.     Helvetica
  267491.     Helvetica
  267492.     Helvetica
  267493. TFA  /  H2O  (2:1)
  267494. 6hr    85%
  267495. hv  2hr
  267496. Untitled preferences-2
  267497. count
  267498. currentpoint 192837465
  267499. currentpoint
  267500. save/chemsave exch def
  267501. %%BeginProcSet: chemdict30 24 10
  267502. % ChemDraw Laser Prep
  267503. % Copyright 198
  267504. 6-1993, Cambridge Scientific Computing, Inc.
  267505. userdict/chemdict30 210 dict put
  267506. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  267507. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  267508. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  267509. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  267510. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  267511. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  267512. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  267513. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  267514. x}b/s
  267515. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  267516. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  267517. 0 cw 2 dv xl
  267518. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  267519. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  267520. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  267521. St 16 and 0 ne{2 
  267522. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  267523. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  267524. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  267525. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  267526. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  267527. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  267528. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  267529. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  267530. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  267531. P P}{sq at 2
  267532. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  267533. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  267534. l w .
  267535. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  267536. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  267537. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  267538. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  267539.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  267540. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  267541. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  267542. 21 -10 27 -8 27 0 cv
  267543. 27 8 21 10 9 6 cv
  267544. -3 2 -3 -2 9 -6 cv
  267545. cp}b/DLB{0 0 M -4.8 4.8 l
  267546. -8 8 -9.6 12 -9.6 16.8 cv
  267547. -9.6 21
  267548. .6 -8 24.6 -4.8 25.8 cv
  267549. -1.6 27 1.6 27 4.8 25.8 cv
  267550. 8 24.6 9.6 21.6 9.6 16.8 cv
  267551. 9.6 12 8 8 4.8 4.8 cv
  267552. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  267553. 0 Y X Y rO ac
  267554. X Y X 0 rO ac
  267555. X 0 0 0 rO ac
  267556. 0 0 0 Y rO ac
  267557. cp}b/Rc{0 0 p M
  267558. 0 Y p l
  267559. X Y p l
  267560. X 0 p l
  267561. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  267562. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  267563. dtransform
  267564. m D 0 lt{n}if sq n D
  267565. CMT dtransform idtransform
  267566. e 2 m e
  267567. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  267568. 32 -0.5 0.5{gs
  267569. 13.5 0 xl
  267570. D 32 s 64 dv 13.5 m D 7 m 24 dv
  267571. -13.5 0 xl
  267572. gr}for
  267573. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  267574. 32 -0.5 0.5{gs
  267575. D 32 s 64 dv 0.65 m D
  267576. gr}for
  267577. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  267578. 32 -0.5 0.5{gs
  267579. D 32 s 64 dv D
  267580. gr}for
  267581. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  267582. 32 -0.5 0.5{gs
  267583. 0 13.5 xl
  267584. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  267585. 0 -13.5 xl
  267586. DLB f
  267587. gr}for
  267588. DLB SM s
  267589. t}{DLB grf}ie}b/gRr{sh{sRmp
  267590. 32 -0.5 0.5{gs
  267591. X 2 dv Y 2 dv xl
  267592. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  267593. X -2 dv Y -2 dv xl
  267594. gr}for
  267595. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  267596. 32 -0.5 0.5{gs
  267597. X 2 dv Y 2 dv xl
  267598. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  267599. X -2 dv Y -2 dv xl
  267600. gr}for
  267601. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  267602. rev{1 -1 sc}if
  267603. 0 lW 2 m xl
  267604. D SA OA
  267605. rad 0 xl
  267606. 180 ro
  267607. 0 lW 2 m xl
  267608. SA OA}b/Aos{X Y M SM 
  267609. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  267610. o 0 lt o 0 lt ne/rev x
  267611. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  267612. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  267613. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  267614. lp 0 p M
  267615. 0 0 0 Y lp ac
  267616. 0 Y 2 dv lp neg o lp ac
  267617. 0 Y 2 dv 0 Y lp ac
  267618. 0 Y lp Y lp ac
  267619. X lp s 0 p M
  267620. X 0 X Y lp ac
  267621. X Y 2 dv X lp a o lp ac
  267622. X Y 2 dv X Y lp ac
  267623. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  267624. A s 180 pA a arc st
  267625. np X Y s Y 2 dv
  267626. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  267627. rO D rlineto
  267628. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  267629. rO lW -2 dv a Y lW 2 dv a rO a p l
  267630. lW -2 dv Y lW 2 dv a p l
  267631. 0 Y p l X Y p l X 0 p l cp f
  267632. 0 0 p M
  267633. 0 Y p l
  267634. X Y p l
  267635. X 0 p l cp
  267636. SM st}{Rr SM st}{rO Y p M rO rO xl
  267637. 0 Y X Y rO ac
  267638. X Y X 0 rO ac
  267639. X 0 0 0 rO ac
  267640. rO neg D xl X Y 0 Y rO ac
  267641. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  267642. -1 -1 sc LB whf}{Asc gs gLB gr
  267643. -0.4 -0
  267644. .4 sc LB whf}{Asc LB gs whf gr
  267645. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  267646. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  267647. gs 3.6 12 sc gOv gr
  267648. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  267649. gs 3.6 12 sc Cr whf gr
  267650. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  267651. 0 -1 p M
  267652. 0 0 1 0 1 ac
  267653. 8 0 8 1 1 ac
  267654. 8 0 16 0 1 ac
  267655. 16 0 16 -1 1 ac
  267656. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  267657. 2 dv D sc
  267658. 1 0 M -1 0 l
  267659. 0 1 M 0 -1 l
  267660. Ast}{XY D X Y dt 0 0 M SM cpt xl
  267661. 2 dv D sc
  267662. 1 0 M -1 0 l
  267663. Ast}{4.5 Aos
  267664. 1 0 M -1 0 l
  267665. 0 1 M 0 -1 l
  267666. 2 0 M 0 0 2 0 360 arc
  267667. Ast}{4.5 Aos
  267668. 1 0 M -1 0 l
  267669. 2 0 M 0 0 2 0 360 arc
  267670. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  267671. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  267672. 1 -1 M -1 -1 l
  267673. 0 2 M 0 -2 l
  267674. Ast}{5 Aos
  267675. 1 -1 M -1 -1 l
  267676. 1 1 M -1 1 l
  267677. 0 2 M 0 -2 l
  267678. Ast}{4.5 Aos
  267679. 1 0 M -1 0 l
  267680. 0 1 M 0 -1 l
  267681. Ast}{4.5 Aos
  267682. 1 0 M -1 0 l
  267683. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  267684. sc DLB gs whf gr
  267685. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  267686. gs 3.6 12 sc Cr whf gr
  267687. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  267688. gs 3.6 12 sc Cr blf gr
  267689. ZLB whf}{Asc LB gs whf gr
  267690. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  267691. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  267692. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  267693. e 2 ix a
  267694. }b/PT{D 2 4 gi al P OP D 1 sc
  267695. o length 6 gt{P 6 g}{e P 8 dv}ie
  267696. D lW 2 m lt{P lW 2 m}if
  267697. 0 e p
  267698. 0 0 p
  267699. 3 -1 r s 3 1 r e s e
  267700. 0 0 p M 1 0 p l
  267701. 0 0 p ap M 1 0 p ap l
  267702. e n e n
  267703. 0 0 p ap M 1 0 p ap l
  267704. P P}b
  267705. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  267706. cvi D 0 eq{P 1}if/nH x
  267707. D hS nH m s
  267708. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  267709. bW 2 dv/bd x
  267710. lW 2 dv e D NH e{D bd p M bd n p l}for
  267711. st gr}{gs 12 OB np
  267712. lW 2 dv 0 xl NH 1 sc
  267713. bW 2 dv wF
  267714.  m nH 1 a dv/bd x
  267715. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  267716. np 0 lW 2 dv o o n p M p l bW 2 dv
  267717. wF m o o p l n p l
  267718. cp f gr}{P}{gs 12 OB/bL x
  267719. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  267720. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  267721. bL nSq 2 m dv D sc
  267722. nSq{.135  .667 .865  .667 1 0 rcurveto
  267723. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  267724. np 0 lW 2 dv o o n p M p l bW 2 dv
  267725. wF m o o p l n p l
  267726. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  267727. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  267728. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  267729. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  267730. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  267731. 5 -1 r dv neg e 5 -1 r dv neg e
  267732. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  267733. %%EndProcSet
  267734. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  267735. 702 138 3 21 
  267736. SPn/origstk x
  267737. 65535 65535 65535 sBg
  267738. 0 0 0 C
  267739. 1413 735 M
  267740. 1413 759 l
  267741. 1093 574 l
  267742. 1103 556 l
  267743. 1690 575 M
  267744. 1700 593 l
  267745. 1413 759 l
  267746. 1413 735 l
  267747. 1450 1090 M
  267748. 1430 1090 l
  267749. 1430 732 l
  267750. 1450 732 l
  267751. 1396 1090 M
  267752. 1376 1090 l
  267753. 1376 732 l
  267754. 1396 732 l
  267755. 1013 2361 M
  267756. 1013 2385 l
  267757. 715 2557 l
  267758. 705 2539 l
  267759. 1406 2588 M
  267760. 1406 2612 l
  267761. 1013 2385 l
  267762. 1013 2361 l
  267763. 1670 2436 M
  267764. 1680 2454 l
  267765. 1406 2612 l
  267766. 1406 2588 l
  267767. f[1 3 1406 2656 1406 2940 ]Bd
  267768. [1 3 1013 2318 1013 2040 ]Bd
  267769. 6060 1880 3520 
  267770. 1880 2 Ar
  267771. 4433 2021 M
  267772. 4433 2045 l
  267773. 4045 2269 l
  267774. 4035 2251 l
  267775. 4428 2086 M
  267776. 4438 2104 l
  267777. 4072 2316 l
  267778. 4062 2298 l
  267779. 4826 2248 M
  267780. 4826 2272 l
  267781. 4433 2045 l
  267782. 4433 2021 l
  267783. 5119 2079 M
  267784. 5129 2097 l
  267785. 4826 2272 l
  267786. 4826 2248 l
  267787. 7013 1801 M
  267788. 7013 1825 l
  267789. 6625 2049 l
  267790. 6615 2031 l
  267791. 7008 1866 M
  267792. 7018 1884 l
  267793. 6652 2096 l
  267794. 6642 2078 l
  267795. 7406 2028 M
  267796. 7406 2052 l
  267797. 7013 1825 l
  267798. 7013 1801 l
  267799. 7766 1820 M
  267800. 7799 1813 l
  267801. 7799 1825 l
  267802. 7406 2052 l
  267803. 7406 2028 l
  267804. 8075 1961 M
  267805. 8065 197
  267806. 7799 1825 l
  267807. 7799 1813 l
  267808. 7804 1804 l
  267809. 8585 1801 M
  267810. 8585 1825 l
  267811. 8295 1993 l
  267812. 8285 1975 l
  267813. f[1 3 8585 1758 8585 1480 ]Bd
  267814. 8978 2028 M
  267815. 8978 2052 l
  267816. 8585 1825 l
  267817. 8585 1801 l
  267818. f[1 3 8978 2096 8978 2380 ]Bd
  267819. 9248 1872 M
  267820. 9258 1890 l
  267821. 8978 2052 l
  267822. 8978 2028 l
  267823. f[1 3 7834 1778 7974 1638 ]Bd
  267824. 7535 1589 M
  267825. 7575 1549 l
  267826. 7819 1793 l
  267827. 7799 1813 l
  267828. 7766 1820 l
  267829. 11660 1880 10620 1880 2 Ar
  267830. 12423 1901 M
  267831. 12423 1925 l
  267832. 12035 2149 l
  267833. 12025 2131 l
  267834. 12418 1966 M
  267835. 12428 1984 l
  267836. 12062 219
  267837. 12052 2178 l
  267838. 12816 2128 M
  267839. 12816 2152 l
  267840. 12423 1925 l
  267841. 12423 1901 l
  267842. 13176 1920 M
  267843. 13209 1913 l
  267844. 13209 1925 l
  267845. 12816 2152 l
  267846. 12816 2128 l
  267847. 13475 2055 M
  267848. 13465 2073 l
  267849. 13209 1925 l
  267850. 13209 1913 l
  267851. 13214 1904 l
  267852. 13885 1964 M
  267853. 13895 1982 l
  267854. 13695 2098 l
  267855. 13685 2080 l
  267856. f[1 3 13245 1877 13389 1733 ]Bd
  267857. 12940 1684 M
  267858. 12980 1644 l
  267859. 13229 1893 l
  267860. 13209 1913 l
  267861. 13176 1920 l
  267862. count origstk sub{P}rp end
  267863. chemsave restore
  267864.     Helvetica
  267865. Palatino
  267866. NHCOCF
  267867. 1) 0.1 eq. TMSB(OTf)
  267868.  0.1 eq. TMSOTf/TfOH
  267869. NHCOCF
  267870. Na, NH
  267871. d.e. = 89/11
  267872. :CHMD
  267873. NHCOCF3
  267874. NHCOCF3
  267875. 1) 0.1 eq. TMSB(OTf)4 or
  267876.  0.1 eq. TMSOTf/TfOH
  267877. Na, NH3
  267878. d.e. = 89/11
  267879.     Helvetica
  267880. Palatinoa
  267881. Untitled preferences-3
  267882. count
  267883. currentpoint 192837465
  267884. currentpoint
  267885. save/chemsave exch def
  267886. %%BeginProcSet: chemdict30 24 10
  267887. % ChemDraw Laser Prep
  267888. % Copyright 198
  267889. 6-1993, Cambridge Scientific Computing, Inc.
  267890. userdict/chemdict30 210 dict put
  267891. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  267892. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  267893. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  267894. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  267895. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  267896. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  267897. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  267898. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  267899. x}b/s
  267900. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  267901. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  267902. 0 cw 2 dv xl
  267903. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  267904. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  267905. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  267906. St 16 and 0 ne{2 
  267907. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  267908. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  267909. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  267910. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  267911. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  267912. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  267913. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  267914. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  267915. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  267916. P P}{sq at 2
  267917. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  267918. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  267919. l w .
  267920. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  267921. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  267922. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  267923. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  267924.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  267925. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  267926. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  267927. 21 -10 27 -8 27 0 cv
  267928. 27 8 21 10 9 6 cv
  267929. -3 2 -3 -2 9 -6 cv
  267930. cp}b/DLB{0 0 M -4.8 4.8 l
  267931. -8 8 -9.6 12 -9.6 16.8 cv
  267932. -9.6 21
  267933. .6 -8 24.6 -4.8 25.8 cv
  267934. -1.6 27 1.6 27 4.8 25.8 cv
  267935. 8 24.6 9.6 21.6 9.6 16.8 cv
  267936. 9.6 12 8 8 4.8 4.8 cv
  267937. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  267938. 0 Y X Y rO ac
  267939. X Y X 0 rO ac
  267940. X 0 0 0 rO ac
  267941. 0 0 0 Y rO ac
  267942. cp}b/Rc{0 0 p M
  267943. 0 Y p l
  267944. X Y p l
  267945. X 0 p l
  267946. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  267947. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  267948. dtransform
  267949. m D 0 lt{n}if sq n D
  267950. CMT dtransform idtransform
  267951. e 2 m e
  267952. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  267953. 32 -0.5 0.5{gs
  267954. 13.5 0 xl
  267955. D 32 s 64 dv 13.5 m D 7 m 24 dv
  267956. -13.5 0 xl
  267957. gr}for
  267958. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  267959. 32 -0.5 0.5{gs
  267960. D 32 s 64 dv 0.65 m D
  267961. gr}for
  267962. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  267963. 32 -0.5 0.5{gs
  267964. D 32 s 64 dv D
  267965. gr}for
  267966. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  267967. 32 -0.5 0.5{gs
  267968. 0 13.5 xl
  267969. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  267970. 0 -13.5 xl
  267971. DLB f
  267972. gr}for
  267973. DLB SM s
  267974. t}{DLB grf}ie}b/gRr{sh{sRmp
  267975. 32 -0.5 0.5{gs
  267976. X 2 dv Y 2 dv xl
  267977. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  267978. X -2 dv Y -2 dv xl
  267979. gr}for
  267980. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  267981. 32 -0.5 0.5{gs
  267982. X 2 dv Y 2 dv xl
  267983. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  267984. X -2 dv Y -2 dv xl
  267985. gr}for
  267986. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  267987. rev{1 -1 sc}if
  267988. 0 lW 2 m xl
  267989. D SA OA
  267990. rad 0 xl
  267991. 180 ro
  267992. 0 lW 2 m xl
  267993. SA OA}b/Aos{X Y M SM 
  267994. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  267995. o 0 lt o 0 lt ne/rev x
  267996. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  267997. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  267998. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  267999. lp 0 p M
  268000. 0 0 0 Y lp ac
  268001. 0 Y 2 dv lp neg o lp ac
  268002. 0 Y 2 dv 0 Y lp ac
  268003. 0 Y lp Y lp ac
  268004. X lp s 0 p M
  268005. X 0 X Y lp ac
  268006. X Y 2 dv X lp a o lp ac
  268007. X Y 2 dv X Y lp ac
  268008. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  268009. A s 180 pA a arc st
  268010. np X Y s Y 2 dv
  268011. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  268012. rO D rlineto
  268013. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  268014. rO lW -2 dv a Y lW 2 dv a rO a p l
  268015. lW -2 dv Y lW 2 dv a p l
  268016. 0 Y p l X Y p l X 0 p l cp f
  268017. 0 0 p M
  268018. 0 Y p l
  268019. X Y p l
  268020. X 0 p l cp
  268021. SM st}{Rr SM st}{rO Y p M rO rO xl
  268022. 0 Y X Y rO ac
  268023. X Y X 0 rO ac
  268024. X 0 0 0 rO ac
  268025. rO neg D xl X Y 0 Y rO ac
  268026. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  268027. -1 -1 sc LB whf}{Asc gs gLB gr
  268028. -0.4 -0
  268029. .4 sc LB whf}{Asc LB gs whf gr
  268030. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  268031. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  268032. gs 3.6 12 sc gOv gr
  268033. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  268034. gs 3.6 12 sc Cr whf gr
  268035. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  268036. 0 -1 p M
  268037. 0 0 1 0 1 ac
  268038. 8 0 8 1 1 ac
  268039. 8 0 16 0 1 ac
  268040. 16 0 16 -1 1 ac
  268041. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  268042. 2 dv D sc
  268043. 1 0 M -1 0 l
  268044. 0 1 M 0 -1 l
  268045. Ast}{XY D X Y dt 0 0 M SM cpt xl
  268046. 2 dv D sc
  268047. 1 0 M -1 0 l
  268048. Ast}{4.5 Aos
  268049. 1 0 M -1 0 l
  268050. 0 1 M 0 -1 l
  268051. 2 0 M 0 0 2 0 360 arc
  268052. Ast}{4.5 Aos
  268053. 1 0 M -1 0 l
  268054. 2 0 M 0 0 2 0 360 arc
  268055. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  268056. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  268057. 1 -1 M -1 -1 l
  268058. 0 2 M 0 -2 l
  268059. Ast}{5 Aos
  268060. 1 -1 M -1 -1 l
  268061. 1 1 M -1 1 l
  268062. 0 2 M 0 -2 l
  268063. Ast}{4.5 Aos
  268064. 1 0 M -1 0 l
  268065. 0 1 M 0 -1 l
  268066. Ast}{4.5 Aos
  268067. 1 0 M -1 0 l
  268068. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  268069. sc DLB gs whf gr
  268070. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  268071. gs 3.6 12 sc Cr whf gr
  268072. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  268073. gs 3.6 12 sc Cr blf gr
  268074. ZLB whf}{Asc LB gs whf gr
  268075. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  268076. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  268077. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  268078. e 2 ix a
  268079. }b/PT{D 2 4 gi al P OP D 1 sc
  268080. o length 6 gt{P 6 g}{e P 8 dv}ie
  268081. D lW 2 m lt{P lW 2 m}if
  268082. 0 e p
  268083. 0 0 p
  268084. 3 -1 r s 3 1 r e s e
  268085. 0 0 p M 1 0 p l
  268086. 0 0 p ap M 1 0 p ap l
  268087. e n e n
  268088. 0 0 p ap M 1 0 p ap l
  268089. P P}b
  268090. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  268091. cvi D 0 eq{P 1}if/nH x
  268092. D hS nH m s
  268093. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  268094. bW 2 dv/bd x
  268095. lW 2 dv e D NH e{D bd p M bd n p l}for
  268096. st gr}{gs 12 OB np
  268097. lW 2 dv 0 xl NH 1 sc
  268098. bW 2 dv wF
  268099.  m nH 1 a dv/bd x
  268100. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  268101. np 0 lW 2 dv o o n p M p l bW 2 dv
  268102. wF m o o p l n p l
  268103. cp f gr}{P}{gs 12 OB/bL x
  268104. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  268105. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  268106. bL nSq 2 m dv D sc
  268107. nSq{.135  .667 .865  .667 1 0 rcurveto
  268108. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  268109. np 0 lW 2 dv o o n p M p l bW 2 dv
  268110. wF m o o p l n p l
  268111. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  268112. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  268113. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  268114. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  268115. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  268116. 5 -1 r dv neg e 5 -1 r dv neg e
  268117. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  268118. %%EndProcSet
  268119. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  268120. 609 136 3 32 SPn/origstk x
  268121. 65535 6553
  268122. 5 65535 sBg
  268123. 0 0 0 C
  268124. 1343 890 M
  268125. 1329 870 l
  268126. 1797 870 l
  268127. 1783 890 l
  268128. 1207 1308 M
  268129. 1185 1316 l
  268130. 1329 870 l
  268131. 1343 890 l
  268132. 1478 1504 M
  268133. 1466 1520 l
  268134. 1185 1316 l
  268135. 1207 1308 l
  268136. 1920 1308 M
  268137. 1931 1312 l
  268138. 1937 1320 l
  268139. 1674 1511 l
  268140. 1662 1495 l
  268141. 1932 1283 M
  268142. 1931 1312 l
  268143. 1920 1308 l
  268144. 1783 890 l
  268145. 1797 870 l
  268146. 1574 2040 M
  268147. 1554 2024 l
  268148. 1554 1690 l
  268149. 1574 1690 l
  268150. 1124 2161 M
  268151. 1126 2139 l
  268152. 1554 2024 l
  268153. 1574 2040 l
  268154. 1868 2165 M
  268155. 1858 2183 l
  268156. 1559 2010 l
  268157. 1569 1992 l
  268158. 1840 22
  268159. 1830 2229 l
  268160. 1523 2050 l
  268161. 1533 2032 l
  268162. 839 1997 M
  268163. 849 1979 l
  268164. 1126 2139 l
  268165. 1124 2161 l
  268166. f[1 9 1125 2150 1125 2604 ]Bd
  268167. 1528 2825 M
  268168. 1508 2837 l
  268169. 1120 2613 l
  268170. 1130 2595 l
  268171. 1528 3285 M
  268172. 1508 3285 l
  268173. 1508 2837 l
  268174. 1528 2825 l
  268175. 1474 3285 M
  268176. 1454 3285 l
  268177. 1454 2862 l
  268178. 1474 2862 l
  268179. 2350 1171 M
  268180. 2390 1217 l
  268181. 1938 1339 l
  268182. 1931 1312 l
  268183. 1932 1283 l
  268184. 2655 1347 M
  268185. 2645 1365 l
  268186. 2390 1217 l
  268187. 2350 1171 l
  268188. 2419 870 M
  268189. 2439 876 l
  268190. 2350 1205 l
  268191. 2330 1199 l
  268192. 2471 884 M
  268193. 2491 
  268194. 890 l
  268195. 2404 1210 l
  268196. 2384 1204 l
  268197. 3142 1190 M
  268198. 3156 1194 l
  268199. 3155 1207 l
  268200. 2855 1380 l
  268201. 2845 1362 l
  268202. 3488 1512 M
  268203. 3466 1518 l
  268204. 3155 1207 l
  268205. 3156 1194 l
  268206. 3170 1194 l
  268207. 3401 1840 M
  268208. 3381 1834 l
  268209. 3466 1518 l
  268210. 3488 1512 l
  268211. 3778 1395 M
  268212. 3784 1415 l
  268213. 3459 1504 l
  268214. 3453 1484 l
  268215. 3792 1447 M
  268216. 3798 1467 l
  268217. 3472 1555 l
  268218. 3466 1535 l
  268219. 3594 2338 M
  268220. 3580 2356 l
  268221. 3419 2077 l
  268222. 3437 2067 l
  268223. 3904 2422 M
  268224. 3898 2442 l
  268225. 3580 2356 l
  268226. 3594 2338 l
  268227. f[1 9 3587 2347 3266 2668 ]Bd
  268228. 2830 2561 M
  268229. 2824 2539 l
  268230. 3269 2658 l
  268231. 3263 2678 l
  268232. 2513 2878 M
  268233. 2499 2864 l
  268234. 2824 2539 l
  268235. 2830 2561 l
  268236. 2551 2916 M
  268237. 2537 2902 l
  268238. 2836 2603 l
  268239. 2850 2617 l
  268240. 2773 1770 M
  268241. 2753 1770 l
  268242. 2753 1530 l
  268243. 2773 1530 l
  268244. 2978 906 M
  268245. 2996 896 l
  268246. 3158 1178 l
  268247. 3156 1194 l
  268248. 3142 1190 l
  268249. 3356 980 M
  268250. 3370 994 l
  268251. 3170 1194 l
  268252. 3156 1194 l
  268253. 3158 1178 l
  268254. 7270 2032 5430 2032 2 Ar
  268255. 8983 1150 M
  268256. 8969 1130 l
  268257. 9437 1130 l
  268258. 9423 1150 l
  268259. 8847 1568 M
  268260. 8825 1576 l
  268261. 8969 1130 l
  268262. 8983 1150 l
  268263. 9118 1764 M
  268264. 9106 1780 l
  268265. 8825 1576 l
  268266. 8847 1568 l
  268267. 9560 1568 M
  268268. 9571 1572 l
  268269. 9577 1580 l
  268270. 9314 1771 l
  268271. 9302 1755 l
  268272. 9572 1543 M
  268273. 9571 1572 l
  268274. 9560 1568 l
  268275. 9423 1150 l
  268276. 9437 1130 l
  268277. 9990 1431 M
  268278. 10030 1477 l
  268279. 9578 1599 l
  268280. 9571 1572 l
  268281. 9572 1543 l
  268282. 10295 1607 M
  268283. 10285 1625 l
  268284. 10030 1477 l
  268285. 9990 1431 l
  268286. 10782 1450 M
  268287. 10796 1454 l
  268288. 10792 1468 l
  268289. 10495 1640 l
  268290. 10485 1622 l
  268291. 10618 1166 M
  268292. 10636 1156 l
  268293. 10798 1438 l
  268294. 10796 1454 l
  268295. 10782 1450 l
  268296. 10966 1270 M
  268297. 10980 1284 l
  268298. 10809 1455 l
  268299. 10796 1454 l
  268300. 10798 1438 l
  268301. 9973 1110 M
  268302. 9993 1110 l
  268303. 9993 1461 l
  268304. 9973 1461 l
  268305. 10027 1110 M
  268306. 10047 1110 l
  268307. 10047 1469 l
  268308. 10027 1469 l
  268309. 9214 2298 M
  268310. 9194 2286 l
  268311. 9194 1950 l
  268312. 9214 1950 l
  268313. 9538 2344 M
  268314. 9532 2364 l
  268315. 9201 2275 l
  268316. 9207 2255 l
  268317. 9524 2396 M
  268318. 9518 2416 l
  268319. 9169 2321 l
  268320. 9175 2301 l
  268321. 8816 2528 M
  268322. 8806 2510 l
  268323. 9194 2286 l
  268324. 9214 2298 l
  268325. f[1 3 8846 2554 9097 2805 ]Bd
  268326. 8460 2529 M
  268327. 8460 2509 l
  268328. 8811 2509 l
  268329. 8811 2529 l
  268330. 9590 2830 M
  268331. 9582 2850 l
  268332. 9132 2850 l
  268333. 9132 2830 l
  268334. 9911 3151 M
  268335. 9903 3171 l
  268336. 9582 2850 l
  268337. 9590 2830 l
  268338. 9936 3100 M
  268339. 9922 3114 l
  268340. 9617 2809 l
  268341. 9631 2795 l
  268342. 10361 3151 M
  268343. 10361 3171 l
  268344. 9903 3171 l
  268345. 9911 3151 l
  268346. 11035 1847 M
  268347. 11011 1847 l
  268348. 10792 1468 l
  268349. 10796 1454 l
  268350. 10809 1455 l
  268351. 11370 1810 M
  268352. 11370 1830 l
  268353. 11008 1830 l
  268354. 11008 1810 l
  268355. 11370 1864 M
  268356. 11370 1884 l
  268357. 11008 1884 l
  268358. 11008 1864 l
  268359. 10249 1968 M
  268360. 10231 1958 l
  268361. 10323 1799 l
  268362. 10341 1809 l
  268363. 10835 2192 M
  268364. 10817 2182 l
  268365. 11011 1847 l
  268366. 11035 1847 
  268367. 10908 2828 M
  268368. 10890 2846 l
  268369. 10778 2428 l
  268370. 10798 2422 l
  268371. f[1 3 10855 2864 10405 3134 ]Bd
  268372. 11368 2952 M
  268373. 11362 2972 l
  268374. 10890 2846 l
  268375. 10908 2828 l
  268376. 6246 1375 M
  268377. 6258 1395 l
  268378. 5980 1395 l
  268379. 5980 1375 l
  268380. 6221 1321 M
  268381. 6221 1341 l
  268382. 5980 1341 l
  268383. 5980 1321 l
  268384. 5790 1100 M
  268385. 5810 1100 l
  268386. 5810 1260 l
  268387. 5790 1260 l
  268388. 5810 1680 M
  268389. 5790 1680 l
  268390. 5790 1500 l
  268391. 5810 1500 l
  268392. 5572 1171 M
  268393. 5586 1157 l
  268394. 5703 1274 l
  268395. 5689 1288 l
  268396. 5519 1559 M
  268397. 5509 1541 l
  268398. 5675 1445 l
  268399. 5685 1463 l
  268400. 6452 1019 M
  268401. 6464 
  268402. U1039 l
  268403. 6258 1395 l
  268404. 6246 1375 l
  268405. 6864 1019 M
  268406. 6868 1029 l
  268407. 6864 1039 l
  268408. 6464 1039 l
  268409. 6452 1019 l
  268410. 6847 1069 M
  268411. 6847 1089 l
  268412. 6487 1089 l
  268413. 6487 1069 l
  268414. 7050 834 M
  268415. 7064 848 l
  268416. 6882 1029 l
  268417. 6868 1029 l
  268418. 6864 1019 l
  268419. 7065 1212 M
  268420. 7051 1226 l
  268421. 6864 1039 l
  268422. 6868 1029 l
  268423. 6882 1029 l
  268424. count origstk sub{P}rp end
  268425. chemsave restore
  268426.     Helvetica
  268427. BOCNH
  268428. CONHBn
  268429. BOCNH
  268430. CONHBn
  268431. Palat
  268432.     DCM, 40
  268433. BOCNH
  268434. CONHBn
  268435. CONHBn
  268436. BOCNH
  268437.     /%r    
  268438. )T    L*X
  268439.     DCM, 40
  268440.     Helvetica
  268441. Palatinoa
  268442. Untitled preferences-4
  268443. count
  268444. currentpoint 192837465
  268445. currentpoint
  268446. save/chemsave exch def
  268447. %%BeginProcSet: chemdict30 24 10
  268448. % ChemDraw Laser Prep
  268449. % Copyright 198
  268450. 6-1993, Cambridge Scientific Computing, Inc.
  268451. userdict/chemdict30 210 dict put
  268452. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  268453. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  268454. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  268455. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  268456. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  268457. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  268458. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  268459. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  268460. x}b/s
  268461. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  268462. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  268463. 0 cw 2 dv xl
  268464. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  268465. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  268466. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  268467. St 16 and 0 ne{2 
  268468. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  268469. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  268470. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  268471. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  268472. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  268473. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  268474. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  268475. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  268476. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  268477. P P}{sq at 2
  268478. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  268479. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  268480. l w .
  268481. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  268482. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  268483. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  268484. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  268485.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  268486. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  268487. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  268488. 21 -10 27 -8 27 0 cv
  268489. 27 8 21 10 9 6 cv
  268490. -3 2 -3 -2 9 -6 cv
  268491. cp}b/DLB{0 0 M -4.8 4.8 l
  268492. -8 8 -9.6 12 -9.6 16.8 cv
  268493. -9.6 21
  268494. .6 -8 24.6 -4.8 25.8 cv
  268495. -1.6 27 1.6 27 4.8 25.8 cv
  268496. 8 24.6 9.6 21.6 9.6 16.8 cv
  268497. 9.6 12 8 8 4.8 4.8 cv
  268498. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  268499. 0 Y X Y rO ac
  268500. X Y X 0 rO ac
  268501. X 0 0 0 rO ac
  268502. 0 0 0 Y rO ac
  268503. cp}b/Rc{0 0 p M
  268504. 0 Y p l
  268505. X Y p l
  268506. X 0 p l
  268507. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  268508. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  268509. dtransform
  268510. m D 0 lt{n}if sq n D
  268511. CMT dtransform idtransform
  268512. e 2 m e
  268513. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  268514. 32 -0.5 0.5{gs
  268515. 13.5 0 xl
  268516. D 32 s 64 dv 13.5 m D 7 m 24 dv
  268517. -13.5 0 xl
  268518. gr}for
  268519. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  268520. 32 -0.5 0.5{gs
  268521. D 32 s 64 dv 0.65 m D
  268522. gr}for
  268523. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  268524. 32 -0.5 0.5{gs
  268525. D 32 s 64 dv D
  268526. gr}for
  268527. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  268528. 32 -0.5 0.5{gs
  268529. 0 13.5 xl
  268530. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  268531. 0 -13.5 xl
  268532. DLB f
  268533. gr}for
  268534. DLB SM s
  268535. t}{DLB grf}ie}b/gRr{sh{sRmp
  268536. 32 -0.5 0.5{gs
  268537. X 2 dv Y 2 dv xl
  268538. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  268539. X -2 dv Y -2 dv xl
  268540. gr}for
  268541. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  268542. 32 -0.5 0.5{gs
  268543. X 2 dv Y 2 dv xl
  268544. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  268545. X -2 dv Y -2 dv xl
  268546. gr}for
  268547. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  268548. rev{1 -1 sc}if
  268549. 0 lW 2 m xl
  268550. D SA OA
  268551. rad 0 xl
  268552. 180 ro
  268553. 0 lW 2 m xl
  268554. SA OA}b/Aos{X Y M SM 
  268555. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  268556. o 0 lt o 0 lt ne/rev x
  268557. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  268558. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  268559. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  268560. lp 0 p M
  268561. 0 0 0 Y lp ac
  268562. 0 Y 2 dv lp neg o lp ac
  268563. 0 Y 2 dv 0 Y lp ac
  268564. 0 Y lp Y lp ac
  268565. X lp s 0 p M
  268566. X 0 X Y lp ac
  268567. X Y 2 dv X lp a o lp ac
  268568. X Y 2 dv X Y lp ac
  268569. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  268570. A s 180 pA a arc st
  268571. np X Y s Y 2 dv
  268572. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  268573. rO D rlineto
  268574. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  268575. rO lW -2 dv a Y lW 2 dv a rO a p l
  268576. lW -2 dv Y lW 2 dv a p l
  268577. 0 Y p l X Y p l X 0 p l cp f
  268578. 0 0 p M
  268579. 0 Y p l
  268580. X Y p l
  268581. X 0 p l cp
  268582. SM st}{Rr SM st}{rO Y p M rO rO xl
  268583. 0 Y X Y rO ac
  268584. X Y X 0 rO ac
  268585. X 0 0 0 rO ac
  268586. rO neg D xl X Y 0 Y rO ac
  268587. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  268588. -1 -1 sc LB whf}{Asc gs gLB gr
  268589. -0.4 -0
  268590. .4 sc LB whf}{Asc LB gs whf gr
  268591. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  268592. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  268593. gs 3.6 12 sc gOv gr
  268594. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  268595. gs 3.6 12 sc Cr whf gr
  268596. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  268597. 0 -1 p M
  268598. 0 0 1 0 1 ac
  268599. 8 0 8 1 1 ac
  268600. 8 0 16 0 1 ac
  268601. 16 0 16 -1 1 ac
  268602. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  268603. 2 dv D sc
  268604. 1 0 M -1 0 l
  268605. 0 1 M 0 -1 l
  268606. Ast}{XY D X Y dt 0 0 M SM cpt xl
  268607. 2 dv D sc
  268608. 1 0 M -1 0 l
  268609. Ast}{4.5 Aos
  268610. 1 0 M -1 0 l
  268611. 0 1 M 0 -1 l
  268612. 2 0 M 0 0 2 0 360 arc
  268613. Ast}{4.5 Aos
  268614. 1 0 M -1 0 l
  268615. 2 0 M 0 0 2 0 360 arc
  268616. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  268617. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  268618. 1 -1 M -1 -1 l
  268619. 0 2 M 0 -2 l
  268620. Ast}{5 Aos
  268621. 1 -1 M -1 -1 l
  268622. 1 1 M -1 1 l
  268623. 0 2 M 0 -2 l
  268624. Ast}{4.5 Aos
  268625. 1 0 M -1 0 l
  268626. 0 1 M 0 -1 l
  268627. Ast}{4.5 Aos
  268628. 1 0 M -1 0 l
  268629. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  268630. sc DLB gs whf gr
  268631. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  268632. gs 3.6 12 sc Cr whf gr
  268633. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  268634. gs 3.6 12 sc Cr blf gr
  268635. ZLB whf}{Asc LB gs whf gr
  268636. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  268637. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  268638. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  268639. e 2 ix a
  268640. }b/PT{D 2 4 gi al P OP D 1 sc
  268641. o length 6 gt{P 6 g}{e P 8 dv}ie
  268642. D lW 2 m lt{P lW 2 m}if
  268643. 0 e p
  268644. 0 0 p
  268645. 3 -1 r s 3 1 r e s e
  268646. 0 0 p M 1 0 p l
  268647. 0 0 p ap M 1 0 p ap l
  268648. e n e n
  268649. 0 0 p ap M 1 0 p ap l
  268650. P P}b
  268651. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  268652. cvi D 0 eq{P 1}if/nH x
  268653. D hS nH m s
  268654. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  268655. bW 2 dv/bd x
  268656. lW 2 dv e D NH e{D bd p M bd n p l}for
  268657. st gr}{gs 12 OB np
  268658. lW 2 dv 0 xl NH 1 sc
  268659. bW 2 dv wF
  268660.  m nH 1 a dv/bd x
  268661. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  268662. np 0 lW 2 dv o o n p M p l bW 2 dv
  268663. wF m o o p l n p l
  268664. cp f gr}{P}{gs 12 OB/bL x
  268665. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  268666. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  268667. bL nSq 2 m dv D sc
  268668. nSq{.135  .667 .865  .667 1 0 rcurveto
  268669. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  268670. np 0 lW 2 dv o o n p M p l bW 2 dv
  268671. wF m o o p l n p l
  268672. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  268673. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  268674. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  268675. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  268676. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  268677. 5 -1 r dv neg e 5 -1 r dv neg e
  268678. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  268679. %%EndProcSet
  268680. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  268681. 471 73 40 75 SPn/origstk x
  268682. 65535 65535 65535 sBg
  268683. 0 0 0 C
  268684. 1324 2218 M
  268685. 1324 2242 l
  268686. 1004 2427 l
  268687. 994 2409 l
  268688. 1287 1890 M
  268689. 1307 1890 l
  268690. 1307 2245 l
  268691. 1287 2245 l
  268692. 1341 1890 M
  268693. 1361 1890 l
  268694. 1361 2245 l
  268695. 1341 2245 l
  268696. 1603 2379 M
  268697. 1593 2397 l
  268698. 1324 2242 l
  268699. 1324 2218 l
  268700. 3910 2190 2530 2190 2 Ar
  268701. 5103 2051 M
  268702. 5103 2075 l
  268703. 4785 2259 l
  268704. 4775 2241 l
  268705. 5066 1730 M
  268706. 5086 1730 l
  268707. 5086 2078 l
  268708. 5066 2078 l
  268709. 5120 1730 M
  268710. 5140 1730 l
  268711. 5140 2078 l
  268712. 5120 2078 l
  268713. 5496 2278 M
  268714. 5496 2302 l
  268715. 5103 2075 l
  268716. 5103 2051 l
  268717. 5533 2630 M
  268718. 5513 2630 l
  268719. 5513 2275 l
  268720. 5533 2275 l
  268721. 5479 2630 M
  268722. 5459 2630 l
  268723. 5459 2275 l
  268724. 5479 2275 l
  268725. 5756 2128 M
  268726. 5766 2146 l
  268727. 5496 2302 l
  268728. 5496 2278 l
  268729. 8190 2230 6710 2230 2 Ar
  268730. 9240 2494 M
  268731. 9220 2514 l
  268732. 9220 2060 l
  268733. 9230 2050 
  268734. 9240 2060 l
  268735. 9590 2494 M
  268736. 9590 2514 l
  268737. 9220 2514 l
  268738. 9240 2494 l
  268739. 9674 2060 M
  268740. 9694 2040 l
  268741. 9694 2410 l
  268742. 9674 2410 l
  268743. 9694 2040 M
  268744. 9674 2060 l
  268745. 9240 2060 l
  268746. 9230 2050 l
  268747. 9240 2040 l
  268748. 8860 2060 M
  268749. 8860 2040 l
  268750. 9220 2040 l
  268751. 9230 2050 l
  268752. 9220 2060 l
  268753. 9220 1720 M
  268754. 9240 1720 l
  268755. 9240 2040 l
  268756. 9230 2050 l
  268757. 9220 2040 l
  268758. 9015 2771 M
  268759. 9001 2757 l
  268760. 9261 2497 l
  268761. 9275 2511 l
  268762. 8977 2733 M
  268763. 8963 2719 l
  268764. 9223 2459 l
  268765. 9237 2473 l
  268766. 9905 2711 M
  268767. 9891 2725 l
  268768. 9765 2599 l
  268769. 9779 258
  268770. count origstk sub{P}rp end
  268771. chemsave restore
  268772.     Helvetica
  268773. Palatino
  268774. PhCOOMe
  268775. LDA, -78
  268776. PhCOOMep
  268777. LDA, -78
  268778.     Helvetica
  268779. Palatinoa
  268780. Untitled preferences-5
  268781. count
  268782. currentpoint 192837465
  268783. currentpoint
  268784. save/chemsave exch def
  268785. %%BeginProcSet: chemdict30 24 10
  268786. % ChemDraw Laser Prep
  268787. % Copyright 198
  268788. 6-1993, Cambridge Scientific Computing, Inc.
  268789. userdict/chemdict30 210 dict put
  268790. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  268791. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  268792. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  268793. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  268794. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  268795. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  268796. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  268797. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  268798. x}b/s
  268799. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  268800. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  268801. 0 cw 2 dv xl
  268802. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  268803. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  268804. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  268805. St 16 and 0 ne{2 
  268806. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  268807. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  268808. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  268809. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  268810. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  268811. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  268812. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  268813. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  268814. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  268815. P P}{sq at 2
  268816. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  268817. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  268818. l w .
  268819. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  268820. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  268821. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  268822. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  268823.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  268824. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  268825. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  268826. 21 -10 27 -8 27 0 cv
  268827. 27 8 21 10 9 6 cv
  268828. -3 2 -3 -2 9 -6 cv
  268829. cp}b/DLB{0 0 M -4.8 4.8 l
  268830. -8 8 -9.6 12 -9.6 16.8 cv
  268831. -9.6 21
  268832. .6 -8 24.6 -4.8 25.8 cv
  268833. -1.6 27 1.6 27 4.8 25.8 cv
  268834. 8 24.6 9.6 21.6 9.6 16.8 cv
  268835. 9.6 12 8 8 4.8 4.8 cv
  268836. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  268837. 0 Y X Y rO ac
  268838. X Y X 0 rO ac
  268839. X 0 0 0 rO ac
  268840. 0 0 0 Y rO ac
  268841. cp}b/Rc{0 0 p M
  268842. 0 Y p l
  268843. X Y p l
  268844. X 0 p l
  268845. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  268846. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  268847. dtransform
  268848. m D 0 lt{n}if sq n D
  268849. CMT dtransform idtransform
  268850. e 2 m e
  268851. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  268852. 32 -0.5 0.5{gs
  268853. 13.5 0 xl
  268854. D 32 s 64 dv 13.5 m D 7 m 24 dv
  268855. -13.5 0 xl
  268856. gr}for
  268857. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  268858. 32 -0.5 0.5{gs
  268859. D 32 s 64 dv 0.65 m D
  268860. gr}for
  268861. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  268862. 32 -0.5 0.5{gs
  268863. D 32 s 64 dv D
  268864. gr}for
  268865. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  268866. 32 -0.5 0.5{gs
  268867. 0 13.5 xl
  268868. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  268869. 0 -13.5 xl
  268870. DLB f
  268871. gr}for
  268872. DLB SM s
  268873. t}{DLB grf}ie}b/gRr{sh{sRmp
  268874. 32 -0.5 0.5{gs
  268875. X 2 dv Y 2 dv xl
  268876. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  268877. X -2 dv Y -2 dv xl
  268878. gr}for
  268879. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  268880. 32 -0.5 0.5{gs
  268881. X 2 dv Y 2 dv xl
  268882. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  268883. X -2 dv Y -2 dv xl
  268884. gr}for
  268885. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  268886. rev{1 -1 sc}if
  268887. 0 lW 2 m xl
  268888. D SA OA
  268889. rad 0 xl
  268890. 180 ro
  268891. 0 lW 2 m xl
  268892. SA OA}b/Aos{X Y M SM 
  268893. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  268894. o 0 lt o 0 lt ne/rev x
  268895. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  268896. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  268897. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  268898. lp 0 p M
  268899. 0 0 0 Y lp ac
  268900. 0 Y 2 dv lp neg o lp ac
  268901. 0 Y 2 dv 0 Y lp ac
  268902. 0 Y lp Y lp ac
  268903. X lp s 0 p M
  268904. X 0 X Y lp ac
  268905. X Y 2 dv X lp a o lp ac
  268906. X Y 2 dv X Y lp ac
  268907. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  268908. A s 180 pA a arc st
  268909. np X Y s Y 2 dv
  268910. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  268911. rO D rlineto
  268912. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  268913. rO lW -2 dv a Y lW 2 dv a rO a p l
  268914. lW -2 dv Y lW 2 dv a p l
  268915. 0 Y p l X Y p l X 0 p l cp f
  268916. 0 0 p M
  268917. 0 Y p l
  268918. X Y p l
  268919. X 0 p l cp
  268920. SM st}{Rr SM st}{rO Y p M rO rO xl
  268921. 0 Y X Y rO ac
  268922. X Y X 0 rO ac
  268923. X 0 0 0 rO ac
  268924. rO neg D xl X Y 0 Y rO ac
  268925. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  268926. -1 -1 sc LB whf}{Asc gs gLB gr
  268927. -0.4 -0
  268928. .4 sc LB whf}{Asc LB gs whf gr
  268929. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  268930. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  268931. gs 3.6 12 sc gOv gr
  268932. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  268933. gs 3.6 12 sc Cr whf gr
  268934. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  268935. 0 -1 p M
  268936. 0 0 1 0 1 ac
  268937. 8 0 8 1 1 ac
  268938. 8 0 16 0 1 ac
  268939. 16 0 16 -1 1 ac
  268940. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  268941. 2 dv D sc
  268942. 1 0 M -1 0 l
  268943. 0 1 M 0 -1 l
  268944. Ast}{XY D X Y dt 0 0 M SM cpt xl
  268945. 2 dv D sc
  268946. 1 0 M -1 0 l
  268947. Ast}{4.5 Aos
  268948. 1 0 M -1 0 l
  268949. 0 1 M 0 -1 l
  268950. 2 0 M 0 0 2 0 360 arc
  268951. Ast}{4.5 Aos
  268952. 1 0 M -1 0 l
  268953. 2 0 M 0 0 2 0 360 arc
  268954. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  268955. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  268956. 1 -1 M -1 -1 l
  268957. 0 2 M 0 -2 l
  268958. Ast}{5 Aos
  268959. 1 -1 M -1 -1 l
  268960. 1 1 M -1 1 l
  268961. 0 2 M 0 -2 l
  268962. Ast}{4.5 Aos
  268963. 1 0 M -1 0 l
  268964. 0 1 M 0 -1 l
  268965. Ast}{4.5 Aos
  268966. 1 0 M -1 0 l
  268967. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  268968. sc DLB gs whf gr
  268969. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  268970. gs 3.6 12 sc Cr whf gr
  268971. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  268972. gs 3.6 12 sc Cr blf gr
  268973. ZLB whf}{Asc LB gs whf gr
  268974. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  268975. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  268976. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  268977. e 2 ix a
  268978. }b/PT{D 2 4 gi al P OP D 1 sc
  268979. o length 6 gt{P 6 g}{e P 8 dv}ie
  268980. D lW 2 m lt{P lW 2 m}if
  268981. 0 e p
  268982. 0 0 p
  268983. 3 -1 r s 3 1 r e s e
  268984. 0 0 p M 1 0 p l
  268985. 0 0 p ap M 1 0 p ap l
  268986. e n e n
  268987. 0 0 p ap M 1 0 p ap l
  268988. P P}b
  268989. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  268990. cvi D 0 eq{P 1}if/nH x
  268991. D hS nH m s
  268992. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  268993. bW 2 dv/bd x
  268994. lW 2 dv e D NH e{D bd p M bd n p l}for
  268995. st gr}{gs 12 OB np
  268996. lW 2 dv 0 xl NH 1 sc
  268997. bW 2 dv wF
  268998.  m nH 1 a dv/bd x
  268999. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  269000. np 0 lW 2 dv o o n p M p l bW 2 dv
  269001. wF m o o p l n p l
  269002. cp f gr}{P}{gs 12 OB/bL x
  269003. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  269004. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  269005. bL nSq 2 m dv D sc
  269006. nSq{.135  .667 .865  .667 1 0 rcurveto
  269007. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  269008. np 0 lW 2 dv o o n p M p l bW 2 dv
  269009. wF m o o p l n p l
  269010. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  269011. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  269012. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  269013. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  269014. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  269015. 5 -1 r dv neg e 5 -1 r dv neg e
  269016. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  269017. %%EndProcSet
  269018. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  269019. 713 115 4 42 SPn/origstk x
  269020. 65535 65535 65535 sBg
  269021. 0 0 0 C
  269022. 260 1884 M
  269023. 240 1884 l
  269024. 240 1430 l
  269025. 260 1430 l
  269026. 206 1884 M
  269027. 186 1884 l
  269028. 186 1430 l
  269029. 206 1430 l
  269030. 314 1884 M
  269031. 294 1884 l
  269032. 294 1430 l
  269033. 314 1430 l
  269034. 240 1100 M
  269035. 260 1100 l
  269036. 60 1430 l
  269037. 240 1430 l
  269038. 260 2240 M
  269039. 240 2240 l
  269040. 240 1884 l
  269041. 260 1884 l
  269042. 2110 1730 650 1730 2 Ar
  269043. 3043 1540 M
  269044. 3036 1530 l
  269045. 3042 1520 l
  269046. 3484 1520 l
  269047. 3490 1530 l
  269048. 3483 1540 l
  269049. 3075 1594 M
  269050. 3075 1574 l
  269051. 3451 1574 l
  269052. 3451 1594 l
  269053. 2928 1894 M
  269054. 2910 1888 l
  269055. 3025 1532 l
  269056. 3036 1530 l
  269057. 3043 1540 l
  269058. 3264 2216 M
  269059. 3264 2240 l
  269060. 2938 2005 l
  269061. 2950 1989 l
  269062. 3620 1958 M
  269063. 3642 1966 l
  269064. 3264 2240 l
  269065. 3264 2216 l
  269066. 3642 1966 M
  269067. 3620 1958 l
  269068. 3483 1540 l
  269069. 3490 1530 l
  269070. 3501 1532 l
  269071.  1273 M
  269072. 3645 1283 l
  269073. 3501 1532 l
  269074. 3490 1530 l
  269075. 3484 1520 l
  269076. 2865 1254 M
  269077. 2883 1244 l
  269078. 3042 1520 l
  269079. 3036 1530 l
  269080. 3025 1532 l
  269081. 5230 1750 4230 1750 2 Ar
  269082. 4603 1331 M
  269083. 4603 1355 l
  269084. 4215 1579 l
  269085. 4205 1561 l
  269086. 4598 1396 M
  269087. 4608 1414 l
  269088. 4242 1626 l
  269089. 4232 1608 l
  269090. 4889 1496 M
  269091. 4879 1514 l
  269092. 4603 1355 l
  269093. 4603 1331 l
  269094. 6353 1560 M
  269095. 6346 1550 l
  269096. 6352 1540 l
  269097. 6794 1540 l
  269098. 6800 1550 l
  269099. 6793 1560 l
  269100. 6385 1614 M
  269101. 6385 1594 l
  269102. 6761 1594 l
  269103. 6761 1614 l
  269104. 6237 1917 M
  269105. 6219 1911 l
  269106. 6335 155
  269107. 6346 1550 l
  269108. 6353 1560 l
  269109. 6574 2236 M
  269110. 6574 2260 l
  269111. 6248 2025 l
  269112. 6260 2009 l
  269113. 6930 1978 M
  269114. 6952 1986 l
  269115. 6574 2260 l
  269116. 6574 2236 l
  269117. 6952 1986 M
  269118. 6930 1978 l
  269119. 6793 1560 l
  269120. 6800 1550 l
  269121. 6811 1552 l
  269122. 6939 1289 M
  269123. 6957 1299 l
  269124. 6811 1552 l
  269125. 6800 1550 l
  269126. 6794 1540 l
  269127. 6177 1279 M
  269128. 6195 1269 l
  269129. 6352 1540 l
  269130. 6346 1550 l
  269131. 6335 1552 l
  269132. 65535 65535 65535 C
  269133. 6679 2111 M
  269134. 6729 2197 l
  269135. 6810 2138 l
  269136. 6760 2052 l
  269137. 6860 2303 M
  269138. 6842 2313 l
  269139. 6681 2035 l
  269140. 6699 2025 l
  269141. 4650 2483
  269142.  4433 2107 8 Ar
  269143. 4420 2633 M
  269144. 4420 2653 l
  269145. 4160 2653 l
  269146. 4160 2633 l
  269147. 4420 2687 M
  269148. 4420 2707 l
  269149. 4160 2707 l
  269150. 4160 2687 l
  269151. 8690 1770 7490 1770 2 Ar
  269152. 10318 1680 M
  269153. 10324 1690 l
  269154. 10320 1700 l
  269155. 9874 1700 l
  269156. 9870 1690 l
  269157. 9876 1680 l
  269158. 10302 1734 M
  269159. 10302 1754 l
  269160. 9892 1754 l
  269161. 9892 1734 l
  269162. 9700 1417 M
  269163. 9718 1407 l
  269164. 9876 1680 l
  269165. 9870 1690 l
  269166. 9857 1689 l
  269167. 10462 1430 M
  269168. 10480 1440 l
  269169. 10337 1689 l
  269170. 10324 1690 l
  269171. 10318 1680 l
  269172. 9598 1976 M
  269173. 9584 1962 l
  269174. 9857 1689 l
  269175. 9870 1690 l
  269176. 9874 1
  269177. 700 l
  269178. 10649 2001 M
  269179. 10641 2021 l
  269180. 10320 1700 l
  269181. 10324 1690 l
  269182. 10337 1689 l
  269183. 11099 2001 M
  269184. 11099 2021 l
  269185. 10641 2021 l
  269186. 10649 2001 l
  269187. 11099 1947 M
  269188. 11099 1967 l
  269189. 10667 1967 l
  269190. 10667 1947 l
  269191. 9794 2242 M
  269192. 9780 2256 l
  269193. 9584 2060 l
  269194. 9598 2046 l
  269195. 13479 1690 M
  269196. 13485 1700 l
  269197. 13481 1710 l
  269198. 13034 1710 l
  269199. 13030 1700 l
  269200. 13036 1690 l
  269201. 13462 1745 M
  269202. 13462 1765 l
  269203. 13053 1765 l
  269204. 13053 1745 l
  269205. 12856 1418 M
  269206. 12874 1408 l
  269207. 13036 1690 l
  269208. 13030 1700 l
  269209. 13017 1699 l
  269210. 13627 1433 M
  269211. 13645 1443 l
  269212. 13498 1699 l
  269213. 13485 1700 l
  269214. 13479 1690 l
  269215. 12784 1961 M
  269216. 12770 1947 l
  269217. 13017 1699 l
  269218. 13030 1700 l
  269219. 13034 1710 l
  269220. 13809 2011 M
  269221. 13801 2031 l
  269222. 13481 1710 l
  269223. 13485 1700 l
  269224. 13498 1699 l
  269225. 14259 2012 M
  269226. 14259 2032 l
  269227. 13801 2031 l
  269228. 13809 2011 l
  269229. 14259 1957 M
  269230. 14259 1977 l
  269231. 13828 1976 l
  269232. 13828 1956 l
  269233. 12150 1730 11470 1730 2 Ar
  269234. 7270 2670 5630 890 44 Ar
  269235. 3930 2378 2250 910 44 Ar
  269236. count origstk sub{P}rp end
  269237. chemsave restore
  269238.     Helvetica
  269239. Palatino
  269240. +1-    85% (GC)
  269241. 62% isolated
  269242. 95% E
  269243. Cp2Zr#
  269244. Cp2Zr
  269245. Cp2Zr?
  269246. Cp2ZrEt2
  269247. &H    t'
  269248. 85% (GC)
  269249. 62% isolated
  269250. 95% E
  269251.     Helvetica
  269252. Palatinoa
  269253. Untitled preferences-1
  269254. count
  269255. currentpoint 192837465
  269256. currentpoint
  269257. save/chemsave exch def
  269258. %%BeginProcSet: chemdict30 24 10
  269259. % ChemDraw Laser Prep
  269260. % Copyright 198
  269261. 6-1993, Cambridge Scientific Computing, Inc.
  269262. userdict/chemdict30 210 dict put
  269263. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  269264. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  269265. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  269266. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  269267. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  269268. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  269269. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  269270. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  269271. x}b/s
  269272. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  269273. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  269274. 0 cw 2 dv xl
  269275. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  269276. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  269277. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  269278. St 16 and 0 ne{2 
  269279. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  269280. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  269281. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  269282. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  269283. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  269284. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  269285. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  269286. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  269287. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  269288. P P}{sq at 2
  269289. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  269290. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  269291. l w .
  269292. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  269293. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  269294. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  269295. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  269296.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  269297. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  269298. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  269299. 21 -10 27 -8 27 0 cv
  269300. 27 8 21 10 9 6 cv
  269301. -3 2 -3 -2 9 -6 cv
  269302. cp}b/DLB{0 0 M -4.8 4.8 l
  269303. -8 8 -9.6 12 -9.6 16.8 cv
  269304. -9.6 21
  269305. .6 -8 24.6 -4.8 25.8 cv
  269306. -1.6 27 1.6 27 4.8 25.8 cv
  269307. 8 24.6 9.6 21.6 9.6 16.8 cv
  269308. 9.6 12 8 8 4.8 4.8 cv
  269309. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  269310. 0 Y X Y rO ac
  269311. X Y X 0 rO ac
  269312. X 0 0 0 rO ac
  269313. 0 0 0 Y rO ac
  269314. cp}b/Rc{0 0 p M
  269315. 0 Y p l
  269316. X Y p l
  269317. X 0 p l
  269318. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  269319. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  269320. dtransform
  269321. m D 0 lt{n}if sq n D
  269322. CMT dtransform idtransform
  269323. e 2 m e
  269324. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  269325. 32 -0.5 0.5{gs
  269326. 13.5 0 xl
  269327. D 32 s 64 dv 13.5 m D 7 m 24 dv
  269328. -13.5 0 xl
  269329. gr}for
  269330. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  269331. 32 -0.5 0.5{gs
  269332. D 32 s 64 dv 0.65 m D
  269333. gr}for
  269334. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  269335. 32 -0.5 0.5{gs
  269336. D 32 s 64 dv D
  269337. gr}for
  269338. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  269339. 32 -0.5 0.5{gs
  269340. 0 13.5 xl
  269341. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  269342. 0 -13.5 xl
  269343. DLB f
  269344. gr}for
  269345. DLB SM s
  269346. t}{DLB grf}ie}b/gRr{sh{sRmp
  269347. 32 -0.5 0.5{gs
  269348. X 2 dv Y 2 dv xl
  269349. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  269350. X -2 dv Y -2 dv xl
  269351. gr}for
  269352. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  269353. 32 -0.5 0.5{gs
  269354. X 2 dv Y 2 dv xl
  269355. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  269356. X -2 dv Y -2 dv xl
  269357. gr}for
  269358. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  269359. rev{1 -1 sc}if
  269360. 0 lW 2 m xl
  269361. D SA OA
  269362. rad 0 xl
  269363. 180 ro
  269364. 0 lW 2 m xl
  269365. SA OA}b/Aos{X Y M SM 
  269366. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  269367. o 0 lt o 0 lt ne/rev x
  269368. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  269369. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  269370. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  269371. lp 0 p M
  269372. 0 0 0 Y lp ac
  269373. 0 Y 2 dv lp neg o lp ac
  269374. 0 Y 2 dv 0 Y lp ac
  269375. 0 Y lp Y lp ac
  269376. X lp s 0 p M
  269377. X 0 X Y lp ac
  269378. X Y 2 dv X lp a o lp ac
  269379. X Y 2 dv X Y lp ac
  269380. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  269381. A s 180 pA a arc st
  269382. np X Y s Y 2 dv
  269383. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  269384. rO D rlineto
  269385. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  269386. rO lW -2 dv a Y lW 2 dv a rO a p l
  269387. lW -2 dv Y lW 2 dv a p l
  269388. 0 Y p l X Y p l X 0 p l cp f
  269389. 0 0 p M
  269390. 0 Y p l
  269391. X Y p l
  269392. X 0 p l cp
  269393. SM st}{Rr SM st}{rO Y p M rO rO xl
  269394. 0 Y X Y rO ac
  269395. X Y X 0 rO ac
  269396. X 0 0 0 rO ac
  269397. rO neg D xl X Y 0 Y rO ac
  269398. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  269399. -1 -1 sc LB whf}{Asc gs gLB gr
  269400. -0.4 -0
  269401. .4 sc LB whf}{Asc LB gs whf gr
  269402. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  269403. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  269404. gs 3.6 12 sc gOv gr
  269405. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  269406. gs 3.6 12 sc Cr whf gr
  269407. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  269408. 0 -1 p M
  269409. 0 0 1 0 1 ac
  269410. 8 0 8 1 1 ac
  269411. 8 0 16 0 1 ac
  269412. 16 0 16 -1 1 ac
  269413. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  269414. 2 dv D sc
  269415. 1 0 M -1 0 l
  269416. 0 1 M 0 -1 l
  269417. Ast}{XY D X Y dt 0 0 M SM cpt xl
  269418. 2 dv D sc
  269419. 1 0 M -1 0 l
  269420. Ast}{4.5 Aos
  269421. 1 0 M -1 0 l
  269422. 0 1 M 0 -1 l
  269423. 2 0 M 0 0 2 0 360 arc
  269424. Ast}{4.5 Aos
  269425. 1 0 M -1 0 l
  269426. 2 0 M 0 0 2 0 360 arc
  269427. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  269428. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  269429. 1 -1 M -1 -1 l
  269430. 0 2 M 0 -2 l
  269431. Ast}{5 Aos
  269432. 1 -1 M -1 -1 l
  269433. 1 1 M -1 1 l
  269434. 0 2 M 0 -2 l
  269435. Ast}{4.5 Aos
  269436. 1 0 M -1 0 l
  269437. 0 1 M 0 -1 l
  269438. Ast}{4.5 Aos
  269439. 1 0 M -1 0 l
  269440. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  269441. sc DLB gs whf gr
  269442. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  269443. gs 3.6 12 sc Cr whf gr
  269444. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  269445. gs 3.6 12 sc Cr blf gr
  269446. ZLB whf}{Asc LB gs whf gr
  269447. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  269448. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  269449. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  269450. e 2 ix a
  269451. }b/PT{D 2 4 gi al P OP D 1 sc
  269452. o length 6 gt{P 6 g}{e P 8 dv}ie
  269453. D lW 2 m lt{P lW 2 m}if
  269454. 0 e p
  269455. 0 0 p
  269456. 3 -1 r s 3 1 r e s e
  269457. 0 0 p M 1 0 p l
  269458. 0 0 p ap M 1 0 p ap l
  269459. e n e n
  269460. 0 0 p ap M 1 0 p ap l
  269461. P P}b
  269462. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  269463. cvi D 0 eq{P 1}if/nH x
  269464. D hS nH m s
  269465. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  269466. bW 2 dv/bd x
  269467. lW 2 dv e D NH e{D bd p M bd n p l}for
  269468. st gr}{gs 12 OB np
  269469. lW 2 dv 0 xl NH 1 sc
  269470. bW 2 dv wF
  269471.  m nH 1 a dv/bd x
  269472. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  269473. np 0 lW 2 dv o o n p M p l bW 2 dv
  269474. wF m o o p l n p l
  269475. cp f gr}{P}{gs 12 OB/bL x
  269476. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  269477. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  269478. bL nSq 2 m dv D sc
  269479. nSq{.135  .667 .865  .667 1 0 rcurveto
  269480. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  269481. np 0 lW 2 dv o o n p M p l bW 2 dv
  269482. wF m o o p l n p l
  269483. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  269484. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  269485. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  269486. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  269487. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  269488. 5 -1 r dv neg e 5 -1 r dv neg e
  269489. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  269490. %%EndProcSet
  269491. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  269492. 426 88 26 46 SPn/origstk x
  269493. 5 65535 65535 sBg
  269494. 0 0 0 C
  269495. 993 1501 M
  269496. 993 1525 l
  269497. 605 1749 l
  269498. 595 1731 l
  269499. 988 1566 M
  269500. 998 1584 l
  269501. 632 1796 l
  269502. 622 1778 l
  269503. 1386 1728 M
  269504. 1386 1752 l
  269505. 993 1525 l
  269506. 993 1501 l
  269507. 1658 1571 M
  269508. 1668 1589 l
  269509. 1386 1752 l
  269510. 1386 1728 l
  269511. 1621 1260 M
  269512. 1639 1250 l
  269513. 1726 1400 l
  269514. 1708 1410 l
  269515. 1987 1291 M
  269516. 2001 1305 l
  269517. 1885 1421 l
  269518. 1871 1407 l
  269519. 2172 1728 M
  269520. 2172 1752 l
  269521. 1900 1595 l
  269522. 1910 1577 l
  269523. 2565 1501 M
  269524. 2565 1525 l
  269525. 2172 1752 l
  269526. 2172 1728 l
  269527. 2963 1731 M
  269528. 2953 1749 l
  269529. 5 1525 l
  269530. 2565 1501 l
  269531. 2936 1778 M
  269532. 2926 1796 l
  269533. 2560 1584 l
  269534. 2570 1566 l
  269535. 5140 1660 3500 1660 2 Ar
  269536. 6197 1333 M
  269537. 6187 1327 l
  269538. 6204 1305 l
  269539. 6580 1088 l
  269540. 6580 1112 l
  269541. 6197 1775 M
  269542. 6177 1787 l
  269543. 6177 1353 l
  269544. 6187 1327 l
  269545. 6197 1333 l
  269546. 6469 1931 M
  269547. 6459 1949 l
  269548. 6177 1787 l
  269549. 6197 1775 l
  269550. 6963 1775 M
  269551. 6983 1787 l
  269552. 6710 1944 l
  269553. 6700 1926 l
  269554. 6963 1333 M
  269555. 6973 1327 l
  269556. 6983 1353 l
  269557. 6983 1787 l
  269558. 6963 1775 l
  269559. 6956 1305 M
  269560. 6973 1327 l
  269561. 6963 1333 l
  269562. 6580 1112 l
  269563. 6580 1088 l
  269564. 6322 2279 M
  269565. 6308 2265 l
  269566. 6485 2088 l
  269567. 6499 2102 l
  269568. 6792 2205 M
  269569. 6778 2219 l
  269570. 6672 2113 l
  269571. 6686 2099 l
  269572. 5862 1171 M
  269573. 5890 1123 l
  269574. 6204 1305 l
  269575. 6187 1327 l
  269576. 6177 1353 l
  269577. 7349 1078 M
  269578. 7383 1122 l
  269579. 6983 1353 l
  269580. 6973 1327 l
  269581. 6956 1305 l
  269582. 7641 1247 M
  269583. 7631 1265 l
  269584. 7383 1122 l
  269585. 7349 1078 l
  269586. count origstk sub{P}rp end
  269587. chemsave restore
  269588.     Helvetica
  269589. Palatino
  269590.     PhMe, 0
  269591. then dry air
  269592. 61%, 100% cis
  269593.     Cp*2ZrMe2
  269594. B(C6F5)3
  269595. Me3Al
  269596.     PhMe, 0
  269597. then dry air
  269598. 61%, 100% cis
  269599.     Helvetica
  269600. Palatinoa
  269601. Untitled Ref Style-1
  269602. count
  269603. currentpoint 192837465
  269604. currentpoint
  269605. save/chemsave exch def
  269606. %%BeginProcSet: chemdict30 24 10
  269607. % ChemDraw Laser Prep
  269608. % Copyright 1986-
  269609. 6-1993, Cambridge Scientific Computing, Inc.
  269610. userdict/chemdict30 210 dict put
  269611. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  269612. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  269613. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  269614. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  269615. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  269616. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  269617. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  269618. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  269619. x}b/s
  269620. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  269621. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  269622. 0 cw 2 dv xl
  269623. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  269624. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  269625. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  269626. St 16 and 0 ne{2 
  269627. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  269628. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  269629. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  269630. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  269631. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  269632. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  269633. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  269634. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  269635. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  269636. P P}{sq at 2
  269637. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  269638. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  269639. l w .
  269640. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  269641. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  269642. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  269643. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  269644.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  269645. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  269646. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  269647. 21 -10 27 -8 27 0 cv
  269648. 27 8 21 10 9 6 cv
  269649. -3 2 -3 -2 9 -6 cv
  269650. cp}b/DLB{0 0 M -4.8 4.8 l
  269651. -8 8 -9.6 12 -9.6 16.8 cv
  269652. -9.6 21
  269653. .6 -8 24.6 -4.8 25.8 cv
  269654. -1.6 27 1.6 27 4.8 25.8 cv
  269655. 8 24.6 9.6 21.6 9.6 16.8 cv
  269656. 9.6 12 8 8 4.8 4.8 cv
  269657. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  269658. 0 Y X Y rO ac
  269659. X Y X 0 rO ac
  269660. X 0 0 0 rO ac
  269661. 0 0 0 Y rO ac
  269662. cp}b/Rc{0 0 p M
  269663. 0 Y p l
  269664. X Y p l
  269665. X 0 p l
  269666. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  269667. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  269668. dtransform
  269669. m D 0 lt{n}if sq n D
  269670. CMT dtransform idtransform
  269671. e 2 m e
  269672. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  269673. 32 -0.5 0.5{gs
  269674. 13.5 0 xl
  269675. D 32 s 64 dv 13.5 m D 7 m 24 dv
  269676. -13.5 0 xl
  269677. gr}for
  269678. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  269679. 32 -0.5 0.5{gs
  269680. D 32 s 64 dv 0.65 m D
  269681. gr}for
  269682. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  269683. 32 -0.5 0.5{gs
  269684. D 32 s 64 dv D
  269685. gr}for
  269686. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  269687. 32 -0.5 0.5{gs
  269688. 0 13.5 xl
  269689. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  269690. 0 -13.5 xl
  269691. DLB f
  269692. gr}for
  269693. DLB SM s
  269694. t}{DLB grf}ie}b/gRr{sh{sRmp
  269695. 32 -0.5 0.5{gs
  269696. X 2 dv Y 2 dv xl
  269697. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  269698. X -2 dv Y -2 dv xl
  269699. gr}for
  269700. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  269701. 32 -0.5 0.5{gs
  269702. X 2 dv Y 2 dv xl
  269703. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  269704. X -2 dv Y -2 dv xl
  269705. gr}for
  269706. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  269707. rev{1 -1 sc}if
  269708. 0 lW 2 m xl
  269709. D SA OA
  269710. rad 0 xl
  269711. 180 ro
  269712. 0 lW 2 m xl
  269713. SA OA}b/Aos{X Y M SM 
  269714. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  269715. o 0 lt o 0 lt ne/rev x
  269716. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  269717. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  269718. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  269719. lp 0 p M
  269720. 0 0 0 Y lp ac
  269721. 0 Y 2 dv lp neg o lp ac
  269722. 0 Y 2 dv 0 Y lp ac
  269723. 0 Y lp Y lp ac
  269724. X lp s 0 p M
  269725. X 0 X Y lp ac
  269726. X Y 2 dv X lp a o lp ac
  269727. X Y 2 dv X Y lp ac
  269728. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  269729. A s 180 pA a arc st
  269730. np X Y s Y 2 dv
  269731. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  269732. rO D rlineto
  269733. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  269734. rO lW -2 dv a Y lW 2 dv a rO a p l
  269735. lW -2 dv Y lW 2 dv a p l
  269736. 0 Y p l X Y p l X 0 p l cp f
  269737. 0 0 p M
  269738. 0 Y p l
  269739. X Y p l
  269740. X 0 p l cp
  269741. SM st}{Rr SM st}{rO Y p M rO rO xl
  269742. 0 Y X Y rO ac
  269743. X Y X 0 rO ac
  269744. X 0 0 0 rO ac
  269745. rO neg D xl X Y 0 Y rO ac
  269746. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  269747. -1 -1 sc LB whf}{Asc gs gLB gr
  269748. -0.4 -0
  269749. .4 sc LB whf}{Asc LB gs whf gr
  269750. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  269751. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  269752. gs 3.6 12 sc gOv gr
  269753. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  269754. gs 3.6 12 sc Cr whf gr
  269755. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  269756. 0 -1 p M
  269757. 0 0 1 0 1 ac
  269758. 8 0 8 1 1 ac
  269759. 8 0 16 0 1 ac
  269760. 16 0 16 -1 1 ac
  269761. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  269762. 2 dv D sc
  269763. 1 0 M -1 0 l
  269764. 0 1 M 0 -1 l
  269765. Ast}{XY D X Y dt 0 0 M SM cpt xl
  269766. 2 dv D sc
  269767. 1 0 M -1 0 l
  269768. Ast}{4.5 Aos
  269769. 1 0 M -1 0 l
  269770. 0 1 M 0 -1 l
  269771. 2 0 M 0 0 2 0 360 arc
  269772. Ast}{4.5 Aos
  269773. 1 0 M -1 0 l
  269774. 2 0 M 0 0 2 0 360 arc
  269775. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  269776. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  269777. 1 -1 M -1 -1 l
  269778. 0 2 M 0 -2 l
  269779. Ast}{5 Aos
  269780. 1 -1 M -1 -1 l
  269781. 1 1 M -1 1 l
  269782. 0 2 M 0 -2 l
  269783. Ast}{4.5 Aos
  269784. 1 0 M -1 0 l
  269785. 0 1 M 0 -1 l
  269786. Ast}{4.5 Aos
  269787. 1 0 M -1 0 l
  269788. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  269789. sc DLB gs whf gr
  269790. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  269791. gs 3.6 12 sc Cr whf gr
  269792. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  269793. gs 3.6 12 sc Cr blf gr
  269794. ZLB whf}{Asc LB gs whf gr
  269795. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  269796. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  269797. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  269798. e 2 ix a
  269799. }b/PT{D 2 4 gi al P OP D 1 sc
  269800. o length 6 gt{P 6 g}{e P 8 dv}ie
  269801. D lW 2 m lt{P lW 2 m}if
  269802. 0 e p
  269803. 0 0 p
  269804. 3 -1 r s 3 1 r e s e
  269805. 0 0 p M 1 0 p l
  269806. 0 0 p ap M 1 0 p ap l
  269807. e n e n
  269808. 0 0 p ap M 1 0 p ap l
  269809. P P}b
  269810. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  269811. cvi D 0 eq{P 1}if/nH x
  269812. D hS nH m s
  269813. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  269814. bW 2 dv/bd x
  269815. lW 2 dv e D NH e{D bd p M bd n p l}for
  269816. st gr}{gs 12 OB np
  269817. lW 2 dv 0 xl NH 1 sc
  269818. bW 2 dv wF
  269819.  m nH 1 a dv/bd x
  269820. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  269821. np 0 lW 2 dv o o n p M p l bW 2 dv
  269822. wF m o o p l n p l
  269823. cp f gr}{P}{gs 12 OB/bL x
  269824. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  269825. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  269826. bL nSq 2 m dv D sc
  269827. nSq{.135  .667 .865  .667 1 0 rcurveto
  269828. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  269829. np 0 lW 2 dv o o n p M p l bW 2 dv
  269830. wF m o o p l n p l
  269831. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  269832. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  269833. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  269834. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  269835. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  269836. 5 -1 r dv neg e 5 -1 r dv neg e
  269837. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  269838. %%EndProcSet
  269839. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  269840. 576 143 3 32 SPn/origstk x
  269841. 65535 65535 65535 sBg
  269842. 0 0 0 C
  269843. 293 1380 M
  269844. 286 1370 l
  269845. 304 1360 l
  269846. 722 1360 l
  269847. 740 1370 l
  269848. 733 1380 l
  269849. 157 1798 M
  269850. 135 1806 l
  269851. 277 1367 l
  269852. 286 1370 l
  269853. 293 1380 l
  269854. 419 1987 M
  269855. 407 2003 l
  269856. 135 1806 l
  269857. 157 1798 l
  269858. 870 1798 M
  269859. 892 1806 l
  269860. 614 2008 l
  269861. 602 1992 l
  269862. 892 1806 M
  269863. 870 1798 l
  269864. 733 1380 l
  269865. 740 1370 l
  269866. 749 1367 l
  269867. 439 1085 M
  269868. 457 1095 l
  269869. 304 1360 l
  269870. 286 1370 l
  269871. 277 1365 l
  269872. 563 1084 M
  269873. 581 1074 l
  269874. 749 1365 l
  269875. 740 1370 l
  269876. 722 1360 l
  269877. 524 2400 M
  269878. 504 2400 l
  269879. 504 2190 l
  269880. 524 2190 l
  269881. 3940 1822 1660 1822 2 Ar
  269882. 4783 1370 M
  269883. 4769 1350 l
  269884. 5204 1350 l
  269885. 5230 1360 l
  269886. 5223 1370 l
  269887. 4647 1788 M
  269888. 4625 1796 l
  269889. 4769 1350 l
  269890. 4783 1370 l
  269891. 4918 1984 M
  269892. 4906 2000 l
  269893. 4625 1796 l
  269894. 4647 1788 l
  269895. 5360 1788 M
  269896. 5382 1796 l
  269897. 5114 1991 l
  269898. 5102 1975 l
  269899. 5382 1796 M
  269900. 5360 1788 l
  269901. 5223 1370 l
  269902. 5230 1360 l
  269903. 5248 1384 l
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  269905. 4994 2400 l
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  269907. 5014 2170 l
  269908. 5371 1060 M
  269909. 5419 1088 l
  269910. 5248 1384 l
  269911. 5230 1360 l
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  269913. f[1 3 4749 1312 4637 1119 ]Bd
  269914. 9327 727 M
  269915. 9339 707 l
  269916. 9572 1110 l
  269917. 9548 1110 l
  269918. 8886 727 M
  269919. 8874 707 l
  269920. 9339 707 l
  269921. 9327 727 l
  269922. 8667 1110 M
  269923. 8643 1110 l
  269924. 8874 707 l
  269925. 8886 727 l
  269926. 8886 1492 M
  269927. 8874 1512 l
  269928. 8643 1110 l
  269929. 8667 1110 l
  269930. 9327 1492 M
  269931. 9333 1502 l
  269932. 9307 1512 l
  269933. 8874 1512 l
  269934. 8886 1492 l
  269935. 9355 1485 M
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  269938. 9548 1110 l
  269939. 9572 1110 l
  269940. f[1 3 8853 1548 8718 1782 ]Bd
  269941. 8205 1905 M
  269942. 8193 1885 l
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  269944. 8550 1905 l
  269945. 8230 1959 M
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  269953. 8205 1905 l
  269954. 9516 1763 M
  269955. 9468 1791 l
  269956. 9307 1512 l
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  269958. 9355 1485 l
  269959. 10020 1885 M
  269960. 10008 1905 l
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  269963. 9983 1939 M
  269964. 9983 19
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  269966. 9650 1939 l
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  269968. 10241 2288 l
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  269971. 10020 1885 l
  269972. 9931 2612 M
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  269985. 9911 2618 l
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  269988. 10474 3155 M
  269989. 10480 3177 l
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  269993. 10464 3096 M
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  270000. 10480 3177 l
  270001. 10474 3155 l
  270002. 10673 2415 M
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  270005. 10799 2845 l
  270006. 10788 2842 l
  270007. 10627 2454 M
  270008. 10647 2448 l
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  270010. 10728 2832 l
  270011. 10691 2397 M
  270012. 10673 2415 l
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  270014. 10241 2288 l
  270015. 10248 2279 l
  270016. 7542 2415 M
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  270042. 7735 3177 l
  270043. 7741 3155 l
  270044. 8284 2612 M
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  270087. 9090 2460 l
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  270090. 8430 3287 M
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  270106. 927 M
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  270111. count origstk sub{P}rp end
  270112. chemsave restore
  270113.     Helvetica
  270114. Palatino
  270115. catalyst, TMSN
  270116. o    ether, rt
  270117. 95% ee
  270118. A    catalyst:
  270119. 2 mol%
  270120. HCHMD
  270121. COCF3g
  270122. COCF3\
  270123. catalyst, TMSN3
  270124.     ether, rtS
  270125. 95% ee
  270126.     catalyst:
  270127. 2 mol%
  270128.     Helvetica
  270129. Palatinoa
  270130. Untitled Ref Style-2
  270131. count
  270132. currentpoint 192837465
  270133. currentpoint
  270134. save/chemsave exch def
  270135. %%BeginProcSet: chemdict30 24 10
  270136. % ChemDraw Laser Prep
  270137. % Copyright 1986-
  270138. 1993, Cambridge Scientific Computing, Inc.
  270139. userdict/chemdict30 210 dict put
  270140. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  270141. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  270142.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  270143. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  270144. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  270145.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  270146. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  270147. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  270148. x}b/sRm
  270149. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270150. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270151. 0 cw 2 dv xl
  270152. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  270153. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  270154. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  270155. St 16 and 0 ne{2 ix
  270156.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  270157. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  270158. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  270159. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  270160. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  270161. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  270162. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  270163. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  270164. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  270165. P P}{sq at 2
  270166. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  270167. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  270168. l w .35
  270169.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  270170. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
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  270172. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  270173. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  270174. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  270175. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  270176. 21 -10 27 -8 27 0 cv
  270177. 27 8 21 10 9 6 cv
  270178. -3 2 -3 -2 9 -6 cv
  270179. cp}b/DLB{0 0 M -4.8 4.8 l
  270180. -8 8 -9.6 12 -9.6 16.8 cv
  270181. -9.6 21.6
  270182.  -8 24.6 -4.8 25.8 cv
  270183. -1.6 27 1.6 27 4.8 25.8 cv
  270184. 8 24.6 9.6 21.6 9.6 16.8 cv
  270185. 9.6 12 8 8 4.8 4.8 cv
  270186. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  270187. 0 Y X Y rO ac
  270188. X Y X 0 rO ac
  270189. X 0 0 0 rO ac
  270190. 0 0 0 Y rO ac
  270191. cp}b/Rc{0 0 p M
  270192. 0 Y p l
  270193. X Y p l
  270194. X 0 p l
  270195. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  270196. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  270197. ransform
  270198. m D 0 lt{n}if sq n D
  270199. CMT dtransform idtransform
  270200. e 2 m e
  270201. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  270202. 32 -0.5 0.5{gs
  270203. 13.5 0 xl
  270204. D 32 s 64 dv 13.5 m D 7 m 24 dv
  270205. -13.5 0 xl
  270206. gr}for
  270207. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  270208. 32 -0.5 0.5{gs
  270209. D 32 s 64 dv 0.65 m D
  270210. gr}for
  270211. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  270212. 32 -0.5 0.5{gs
  270213. D 32 s 64 dv D
  270214. gr}for
  270215. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  270216. 32 -0.5 0.5{gs
  270217. 0 13.5 xl
  270218. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  270219. 0 -13.5 xl
  270220. DLB f
  270221. gr}for
  270222. DLB SM st}
  270223. {DLB grf}ie}b/gRr{sh{sRmp
  270224. 32 -0.5 0.5{gs
  270225. X 2 dv Y 2 dv xl
  270226. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270227. X -2 dv Y -2 dv xl
  270228. gr}for
  270229. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  270230. 32 -0.5 0.5{gs
  270231. X 2 dv Y 2 dv xl
  270232. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270233. X -2 dv Y -2 dv xl
  270234. gr}for
  270235. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  270236. rev{1 -1 sc}if
  270237. 0 lW 2 m xl
  270238. D SA OA
  270239. rad 0 xl
  270240. 180 ro
  270241. 0 lW 2 m xl
  270242. SA OA}b/Aos{X Y M SM cp
  270243. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  270244. o 0 lt o 0 lt ne/rev x
  270245. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  270246. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  270247. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  270248. lp 0 p M
  270249. 0 0 0 Y lp ac
  270250. 0 Y 2 dv lp neg o lp ac
  270251. 0 Y 2 dv 0 Y lp ac
  270252. 0 Y lp Y lp ac
  270253. X lp s 0 p M
  270254. X 0 X Y lp ac
  270255. X Y 2 dv X lp a o lp ac
  270256. X Y 2 dv X Y lp ac
  270257. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  270258. s 180 pA a arc st
  270259. np X Y s Y 2 dv
  270260. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  270261. rO D rlineto
  270262. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  270263. rO lW -2 dv a Y lW 2 dv a rO a p l
  270264. lW -2 dv Y lW 2 dv a p l
  270265. 0 Y p l X Y p l X 0 p l cp f
  270266. 0 0 p M
  270267. 0 Y p l
  270268. X Y p l
  270269. X 0 p l cp
  270270. SM st}{Rr SM st}{rO Y p M rO rO xl
  270271. 0 Y X Y rO ac
  270272. X Y X 0 rO ac
  270273. X 0 0 0 rO ac
  270274. rO neg D xl X Y 0 Y rO ac
  270275. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  270276. -1 -1 sc LB whf}{Asc gs gLB gr
  270277. -0.4 -0.4
  270278.  sc LB whf}{Asc LB gs whf gr
  270279. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  270280. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  270281. gs 3.6 12 sc gOv gr
  270282. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  270283. gs 3.6 12 sc Cr whf gr
  270284. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  270285. 0 -1 p M
  270286. 0 0 1 0 1 ac
  270287. 8 0 8 1 1 ac
  270288. 8 0 16 0 1 ac
  270289. 16 0 16 -1 1 ac
  270290. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  270291. 2 dv D sc
  270292. 1 0 M -1 0 l
  270293. 0 1 M 0 -1 l
  270294. t}{XY D X Y dt 0 0 M SM cpt xl
  270295. 2 dv D sc
  270296. 1 0 M -1 0 l
  270297. Ast}{4.5 Aos
  270298. 1 0 M -1 0 l
  270299. 0 1 M 0 -1 l
  270300. 2 0 M 0 0 2 0 360 arc
  270301. Ast}{4.5 Aos
  270302. 1 0 M -1 0 l
  270303. 2 0 M 0 0 2 0 360 arc
  270304. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  270305. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  270306. 1 -1 M -1 -1 l
  270307. 0 2 M 0 -2 l
  270308. Ast}{5 Aos
  270309. 1 -1 M -1 -1 l
  270310. 1 1 M -1 1 l
  270311. 0 2 M 0 -2 l
  270312. Ast}{4.5 Aos
  270313. 1 0 M -1 0 l
  270314. 0 1 M 0 -1 l
  270315. Ast}{4.5 Aos
  270316. 1 0 M -1 0 l
  270317. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  270318.  DLB gs whf gr
  270319. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  270320. gs 3.6 12 sc Cr whf gr
  270321. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  270322. gs 3.6 12 sc Cr blf gr
  270323. ZLB whf}{Asc LB gs whf gr
  270324. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  270325. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  270326. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  270327. e 2 ix a}b
  270328. /PT{D 2 4 gi al P OP D 1 sc
  270329. o length 6 gt{P 6 g}{e P 8 dv}ie
  270330. D lW 2 m lt{P lW 2 m}if
  270331. 0 e p
  270332. 0 0 p
  270333. 3 -1 r s 3 1 r e s e
  270334. 0 0 p M 1 0 p l
  270335. 0 0 p ap M 1 0 p ap l
  270336. e n e n
  270337. 0 0 p ap M 1 0 p ap l
  270338. P P}b
  270339. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  270340. cvi D 0 eq{P 1}if/nH x
  270341. D hS nH m s
  270342. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  270343. bW 2 dv/bd x
  270344. lW 2 dv e D NH e{D bd p M bd n p l}for
  270345. st gr}{gs 12 OB np
  270346. lW 2 dv 0 xl NH 1 sc
  270347. bW 2 dv wF m
  270348.  nH 1 a dv/bd x
  270349. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  270350. np 0 lW 2 dv o o n p M p l bW 2 dv
  270351. wF m o o p l n p l
  270352. cp f gr}{P}{gs 12 OB/bL x
  270353. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  270354. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  270355. bL nSq 2 m dv D sc
  270356. nSq{.135  .667 .865  .667 1 0 rcurveto
  270357. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  270358. np 0 lW 2 dv o o n p M p l bW 2 dv
  270359. wF m o o p l n p l
  270360. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  270361. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  270362. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  270363. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  270364. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  270365. 5 -1 r dv neg e 5 -1 r dv neg e
  270366. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  270367. B    Vs[
  270368. EndProcSet
  270369. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  270370. 2675 1340 413 460 SPn/origstk x
  270371. 65535 65535 65535 sBg
  270372. 0 0 0 C
  270373. 2756 2832 M
  270374. 2752 2856 l
  270375. 2417 2521 l
  270376. 2431 2507 l
  270377. 3297 2579 M
  270378. 3297 2601 l
  270379. 2752 2856 l
  270380. 2756 2832 l
  270381. 3838 2838 M
  270382. 3838 2860 l
  270383. 3297 2601 l
  270384. 3297 2579 l
  270385. 4272 2647 M
  270386. 4280 2665 l
  270387. 3838 2860 l
  270388. 3838 2838 l
  270389. 3251 2106 M
  270390. 3271 2106 l
  270391. 3271 2606 l
  270392. 3251 2606 l
  270393. 3323 2106 M
  270394. 3343 2106 l
  270395. 3343 2607 l
  270396. 3323 2607 l
  270397. f[1 4 2754 2898 2754 339
  270398. 0 ]Bd
  270399. 2229 3722 M
  270400. 2219 3716 l
  270401. 2220 3704 l
  270402. 2749 3435 l
  270403. 2759 3453 l
  270404. 1740 3355 M
  270405. 1752 3339 l
  270406. 2220 3704 l
  270407. 2219 3716 l
  270408. 2209 3721 l
  270409. 2229 4316 M
  270410. 2209 4316 l
  270411. 2209 3721 l
  270412. 2219 3716 l
  270413. 2229 3722 l
  270414. 7226 2782 M
  270415. 7222 2806 l
  270416. 6885 2469 l
  270417. 6899 2455 l
  270418. 7767 2529 M
  270419. 7767 2551 l
  270420. 7222 2806 l
  270421. 7226 2782 l
  270422. 8308 2788 M
  270423. 8308 2810 l
  270424. 7767 2551 l
  270425. 7767 2529 l
  270426. 8740 2598 M
  270427. 8748 2616 l
  270428. 8308 2810 l
  270429. 8308 2788 l
  270430. f[1 4 7224 2848 7224 3340 ]Bd
  270431. 6699 3672 M
  270432. 6689 3666 l
  270433. 0 3654 l
  270434. 7219 3385 l
  270435. 7229 3403 l
  270436. 6210 3305 M
  270437. 6222 3289 l
  270438. 6690 3654 l
  270439. 6689 3666 l
  270440. 6679 3671 l
  270441. 6699 4266 M
  270442. 6679 4266 l
  270443. 6679 3671 l
  270444. 6689 3666 l
  270445. 6699 3672 l
  270446. f[1 4 7767 2487 7767 2060 ]Bd
  270447. 10566 2822 M
  270448. 10562 2846 l
  270449. 10225 2509 l
  270450. 10239 2495 l
  270451. 11096 2574 M
  270452. 11107 2580 l
  270453. 11107 2591 l
  270454. 10562 2846 l
  270455. 10566 2822 l
  270456. 11648 2828 M
  270457. 11648 2850 l
  270458. 11107 2591 l
  270459. 11107 2580 l
  270460. 11118 2574 l
  270461. 12080 2638 M
  270462. 12088 2656 l
  270463. 11648 2850 l
  270464. 11648 2828 l
  270465. f[1 4 10564 2888 10564 3380
  270466. 10039 3712 M
  270467. 10029 3706 l
  270468. 10030 3694 l
  270469. 10559 3425 l
  270470. 10569 3443 l
  270471. 9550 3345 M
  270472. 9562 3329 l
  270473. 10030 3694 l
  270474. 10029 3706 l
  270475. 10019 3711 l
  270476. 10039 4306 M
  270477. 10019 4306 l
  270478. 10019 3711 l
  270479. 10029 3706 l
  270480. 10039 3712 l
  270481. 11047 2100 M
  270482. 11167 2100 l
  270483. 11118 2574 l
  270484. 11107 2580 l
  270485. 11096 2574 l
  270486. 6010 2940 4530 2940 2 Ar
  270487. 2806 5592 M
  270488. 2802 5616 l
  270489. 2465 5279 l
  270490. 2479 5265 l
  270491. 3347 5339 M
  270492. 3347 5361 l
  270493. 2802 5616 l
  270494. 2806 5592 l
  270495. 3888 5598 M
  270496. 3888 5620 l
  270497. 3347 5361 l
  270498. 3347 5339 l
  270499. 320 5408 M
  270500. 4328 5426 l
  270501. 3888 5620 l
  270502. 3888 5598 l
  270503. f[1 4 2804 5658 2804 6150 ]Bd
  270504. 2279 6482 M
  270505. 2269 6476 l
  270506. 2270 6464 l
  270507. 2799 6195 l
  270508. 2809 6213 l
  270509. 1790 6115 M
  270510. 1802 6099 l
  270511. 2270 6464 l
  270512. 2269 6476 l
  270513. 2259 6481 l
  270514. 2279 7076 M
  270515. 2259 7076 l
  270516. 2259 6481 l
  270517. 2269 6476 l
  270518. 2279 6482 l
  270519. f[1 4 3347 5297 3347 4868 ]Bd
  270520. 6990 5780 4790 5780 2 Ar
  270521. 8326 5632 M
  270522. 8322 5656 l
  270523. 7985 5319 l
  270524. 7999 5305 l
  270525. 8867 5379 M
  270526. 8867 5401 l
  270527. 8322 5656 l
  270528. 8326 5632 l
  270529. 9398 5633 M
  270530. 9418 5665 l
  270531. 8867 5401 l
  270532.  5379 l
  270533. f[1 4 8324 5698 8324 6190 ]Bd
  270534. 7799 6522 M
  270535. 7789 6516 l
  270536. 7790 6504 l
  270537. 8319 6235 l
  270538. 8329 6253 l
  270539. 7310 6155 M
  270540. 7322 6139 l
  270541. 7790 6504 l
  270542. 7789 6516 l
  270543. 7779 6521 l
  270544. 7799 7116 M
  270545. 7779 7116 l
  270546. 7779 6521 l
  270547. 7789 6516 l
  270548. 7799 6522 l
  270549. f[1 4 8913 5368 9282 5184 ]Bd
  270550. 9394 5239 M
  270551. 9414 5239 l
  270552. 9418 5665 l
  270553. 9398 5633 l
  270554. count origstk sub{P}rp end
  270555. chemsave restore
  270556.     Helvetica
  270557. BocHN
  270558. BocHN
  270559. BocHN
  270560. Times
  270561. Reducing Agent
  270562. BocHN
  270563. RT   1hr
  270564. BocHN
  270565. NHBoc:
  270566. NHBoc<
  270567. NHBocT
  270568. NHBoc
  270569. NHBoc
  270570. Reducing Agent
  270571. RT   1hr
  270572.     Helvetica
  270573. Times
  270574. Untitled Ref Style-2
  270575. count
  270576. currentpoint 192837465
  270577. currentpoint
  270578. save/chemsave exch def
  270579. %%BeginProcSet: chemdict30 24 10
  270580. % ChemDraw Laser Prep
  270581. % Copyright 1986-
  270582. 1993, Cambridge Scientific Computing, Inc.
  270583. userdict/chemdict30 210 dict put
  270584. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  270585. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  270586.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  270587. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  270588. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  270589.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  270590. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  270591. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  270592. x}b/sRm
  270593. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270594. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270595. 0 cw 2 dv xl
  270596. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  270597. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  270598. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  270599. St 16 and 0 ne{2 ix
  270600.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  270601. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  270602. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  270603. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  270604. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  270605. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  270606. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  270607. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  270608. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  270609. P P}{sq at 2
  270610. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  270611. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  270612. l w .35
  270613.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  270614. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  270615. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  270616. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  270617. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  270618. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  270619. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  270620. 21 -10 27 -8 27 0 cv
  270621. 27 8 21 10 9 6 cv
  270622. -3 2 -3 -2 9 -6 cv
  270623. cp}b/DLB{0 0 M -4.8 4.8 l
  270624. -8 8 -9.6 12 -9.6 16.8 cv
  270625. -9.6 21.6
  270626.  -8 24.6 -4.8 25.8 cv
  270627. -1.6 27 1.6 27 4.8 25.8 cv
  270628. 8 24.6 9.6 21.6 9.6 16.8 cv
  270629. 9.6 12 8 8 4.8 4.8 cv
  270630. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  270631. 0 Y X Y rO ac
  270632. X Y X 0 rO ac
  270633. X 0 0 0 rO ac
  270634. 0 0 0 Y rO ac
  270635. cp}b/Rc{0 0 p M
  270636. 0 Y p l
  270637. X Y p l
  270638. X 0 p l
  270639. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  270640. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  270641. ransform
  270642. m D 0 lt{n}if sq n D
  270643. CMT dtransform idtransform
  270644. e 2 m e
  270645. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  270646. 32 -0.5 0.5{gs
  270647. 13.5 0 xl
  270648. D 32 s 64 dv 13.5 m D 7 m 24 dv
  270649. -13.5 0 xl
  270650. gr}for
  270651. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  270652. 32 -0.5 0.5{gs
  270653. D 32 s 64 dv 0.65 m D
  270654. gr}for
  270655. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  270656. 32 -0.5 0.5{gs
  270657. D 32 s 64 dv D
  270658. gr}for
  270659. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  270660. 32 -0.5 0.5{gs
  270661. 0 13.5 xl
  270662. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  270663. 0 -13.5 xl
  270664. DLB f
  270665. gr}for
  270666. DLB SM st}
  270667. {DLB grf}ie}b/gRr{sh{sRmp
  270668. 32 -0.5 0.5{gs
  270669. X 2 dv Y 2 dv xl
  270670. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270671. X -2 dv Y -2 dv xl
  270672. gr}for
  270673. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  270674. 32 -0.5 0.5{gs
  270675. X 2 dv Y 2 dv xl
  270676. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270677. X -2 dv Y -2 dv xl
  270678. gr}for
  270679. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  270680. rev{1 -1 sc}if
  270681. 0 lW 2 m xl
  270682. D SA OA
  270683. rad 0 xl
  270684. 180 ro
  270685. 0 lW 2 m xl
  270686. SA OA}b/Aos{X Y M SM cp
  270687. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  270688. o 0 lt o 0 lt ne/rev x
  270689. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  270690. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  270691. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  270692. lp 0 p M
  270693. 0 0 0 Y lp ac
  270694. 0 Y 2 dv lp neg o lp ac
  270695. 0 Y 2 dv 0 Y lp ac
  270696. 0 Y lp Y lp ac
  270697. X lp s 0 p M
  270698. X 0 X Y lp ac
  270699. X Y 2 dv X lp a o lp ac
  270700. X Y 2 dv X Y lp ac
  270701. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  270702. s 180 pA a arc st
  270703. np X Y s Y 2 dv
  270704. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  270705. rO D rlineto
  270706. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  270707. rO lW -2 dv a Y lW 2 dv a rO a p l
  270708. lW -2 dv Y lW 2 dv a p l
  270709. 0 Y p l X Y p l X 0 p l cp f
  270710. 0 0 p M
  270711. 0 Y p l
  270712. X Y p l
  270713. X 0 p l cp
  270714. SM st}{Rr SM st}{rO Y p M rO rO xl
  270715. 0 Y X Y rO ac
  270716. X Y X 0 rO ac
  270717. X 0 0 0 rO ac
  270718. rO neg D xl X Y 0 Y rO ac
  270719. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  270720. -1 -1 sc LB whf}{Asc gs gLB gr
  270721. -0.4 -0.4
  270722.  sc LB whf}{Asc LB gs whf gr
  270723. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  270724. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  270725. gs 3.6 12 sc gOv gr
  270726. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  270727. gs 3.6 12 sc Cr whf gr
  270728. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  270729. 0 -1 p M
  270730. 0 0 1 0 1 ac
  270731. 8 0 8 1 1 ac
  270732. 8 0 16 0 1 ac
  270733. 16 0 16 -1 1 ac
  270734. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  270735. 2 dv D sc
  270736. 1 0 M -1 0 l
  270737. 0 1 M 0 -1 l
  270738. t}{XY D X Y dt 0 0 M SM cpt xl
  270739. 2 dv D sc
  270740. 1 0 M -1 0 l
  270741. Ast}{4.5 Aos
  270742. 1 0 M -1 0 l
  270743. 0 1 M 0 -1 l
  270744. 2 0 M 0 0 2 0 360 arc
  270745. Ast}{4.5 Aos
  270746. 1 0 M -1 0 l
  270747. 2 0 M 0 0 2 0 360 arc
  270748. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  270749. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  270750. 1 -1 M -1 -1 l
  270751. 0 2 M 0 -2 l
  270752. Ast}{5 Aos
  270753. 1 -1 M -1 -1 l
  270754. 1 1 M -1 1 l
  270755. 0 2 M 0 -2 l
  270756. Ast}{4.5 Aos
  270757. 1 0 M -1 0 l
  270758. 0 1 M 0 -1 l
  270759. Ast}{4.5 Aos
  270760. 1 0 M -1 0 l
  270761. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  270762.  DLB gs whf gr
  270763. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  270764. gs 3.6 12 sc Cr whf gr
  270765. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  270766. gs 3.6 12 sc Cr blf gr
  270767. ZLB whf}{Asc LB gs whf gr
  270768. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  270769. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  270770. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  270771. e 2 ix a}b
  270772. /PT{D 2 4 gi al P OP D 1 sc
  270773. o length 6 gt{P 6 g}{e P 8 dv}ie
  270774. D lW 2 m lt{P lW 2 m}if
  270775. 0 e p
  270776. 0 0 p
  270777. 3 -1 r s 3 1 r e s e
  270778. 0 0 p M 1 0 p l
  270779. 0 0 p ap M 1 0 p ap l
  270780. e n e n
  270781. 0 0 p ap M 1 0 p ap l
  270782. P P}b
  270783. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  270784. cvi D 0 eq{P 1}if/nH x
  270785. D hS nH m s
  270786. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  270787. bW 2 dv/bd x
  270788. lW 2 dv e D NH e{D bd p M bd n p l}for
  270789. st gr}{gs 12 OB np
  270790. lW 2 dv 0 xl NH 1 sc
  270791. bW 2 dv wF m
  270792.  nH 1 a dv/bd x
  270793. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  270794. np 0 lW 2 dv o o n p M p l bW 2 dv
  270795. wF m o o p l n p l
  270796. cp f gr}{P}{gs 12 OB/bL x
  270797. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  270798. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  270799. bL nSq 2 m dv D sc
  270800. nSq{.135  .667 .865  .667 1 0 rcurveto
  270801. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  270802. np 0 lW 2 dv o o n p M p l bW 2 dv
  270803. wF m o o p l n p l
  270804. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  270805. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  270806. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  270807. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  270808. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  270809. 5 -1 r dv neg e 5 -1 r dv neg e
  270810. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  270811. %%EndProcSet
  270812. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  270813. 2700 360 495 795 SPn/origstk x
  270814. 65535 65535 65535 sBg
  270815. 0 0 0 C
  270816. 2592 3876 M
  270817. 2592 3900 l
  270818. 2171 4142 l
  270819. 2161 4124 l
  270820. 3018 4121 M
  270821. 3008 4139 l
  270822. 2592 3900 l
  270823. 2592 3876 l
  270824. 2546 3402 M
  270825. 2566 3402 l
  270826. 2566 3908 l
  270827. 2546 3908 l
  270828. 2618 3402 M
  270829. 2638 3402 l
  270830. 2638 3908 l
  270831. 2618 3908 l
  270832. 6500 3800 4460 3800 2 Ar
  270833. 7892 4156 M
  270834. 7892 4180 l
  270835. 7471 4422 l
  270836. 7461 4404 l
  270837. 8307 4395 M
  270838. 8297 4413 l
  270839. 7892 4180 
  270840. 7892 4156 l
  270841. 7846 3682 M
  270842. 7866 3682 l
  270843. 7866 4188 l
  270844. 7846 4188 l
  270845. 7918 3682 M
  270846. 7938 3682 l
  270847. 7938 4188 l
  270848. 7918 4188 l
  270849. 11000 3920 9640 3920 2 Ar
  270850. 12072 4196 M
  270851. 12072 4220 l
  270852. 11651 4462 l
  270853. 11641 4444 l
  270854. 12490 4436 M
  270855. 12480 4454 l
  270856. 12072 4220 l
  270857. 12072 4196 l
  270858. 12026 3722 M
  270859. 12046 3722 l
  270860. 12046 4228 l
  270861. 12026 4228 l
  270862. 12098 3722 M
  270863. 12118 3722 l
  270864. 12118 4228 l
  270865. 12098 4228 l
  270866. count origstk sub{P}rp end
  270867. chemsave restore
  270868.     Helvetica
  270869. Times
  270870. XMgN(OMe)Me
  270871. N(OMe)Me
  270872. PhMgX
  270873. N(OMe)Me
  270874. XMgN(OMe)Me
  270875. PhMgX
  270876.     Helvetica
  270877. Times
  270878. Untitled Ref Style-3
  270879. count
  270880. currentpoint 192837465
  270881. currentpoint
  270882. save/chemsave exch def
  270883. %%BeginProcSet: chemdict30 24 10
  270884. % ChemDraw Laser Prep
  270885. % Copyright 1986-
  270886. 1993, Cambridge Scientific Computing, Inc.
  270887. userdict/chemdict30 210 dict put
  270888. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  270889. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  270890.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  270891. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  270892. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  270893.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  270894. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  270895. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  270896. x}b/sRm
  270897. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270898. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  270899. 0 cw 2 dv xl
  270900. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  270901. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  270902. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  270903. St 16 and 0 ne{2 ix
  270904.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  270905. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  270906. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  270907. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  270908. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  270909. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  270910. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  270911. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  270912. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  270913. P P}{sq at 2
  270914. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  270915. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  270916. l w .35
  270917.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  270918. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  270919. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  270920. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  270921. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  270922. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  270923. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  270924. 21 -10 27 -8 27 0 cv
  270925. 27 8 21 10 9 6 cv
  270926. -3 2 -3 -2 9 -6 cv
  270927. cp}b/DLB{0 0 M -4.8 4.8 l
  270928. -8 8 -9.6 12 -9.6 16.8 cv
  270929. -9.6 21.6
  270930.  -8 24.6 -4.8 25.8 cv
  270931. -1.6 27 1.6 27 4.8 25.8 cv
  270932. 8 24.6 9.6 21.6 9.6 16.8 cv
  270933. 9.6 12 8 8 4.8 4.8 cv
  270934. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  270935. 0 Y X Y rO ac
  270936. X Y X 0 rO ac
  270937. X 0 0 0 rO ac
  270938. 0 0 0 Y rO ac
  270939. cp}b/Rc{0 0 p M
  270940. 0 Y p l
  270941. X Y p l
  270942. X 0 p l
  270943. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  270944. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  270945. ransform
  270946. m D 0 lt{n}if sq n D
  270947. CMT dtransform idtransform
  270948. e 2 m e
  270949. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  270950. 32 -0.5 0.5{gs
  270951. 13.5 0 xl
  270952. D 32 s 64 dv 13.5 m D 7 m 24 dv
  270953. -13.5 0 xl
  270954. gr}for
  270955. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  270956. 32 -0.5 0.5{gs
  270957. D 32 s 64 dv 0.65 m D
  270958. gr}for
  270959. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  270960. 32 -0.5 0.5{gs
  270961. D 32 s 64 dv D
  270962. gr}for
  270963. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  270964. 32 -0.5 0.5{gs
  270965. 0 13.5 xl
  270966. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  270967. 0 -13.5 xl
  270968. DLB f
  270969. gr}for
  270970. DLB SM st}
  270971. {DLB grf}ie}b/gRr{sh{sRmp
  270972. 32 -0.5 0.5{gs
  270973. X 2 dv Y 2 dv xl
  270974. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270975. X -2 dv Y -2 dv xl
  270976. gr}for
  270977. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  270978. 32 -0.5 0.5{gs
  270979. X 2 dv Y 2 dv xl
  270980. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  270981. X -2 dv Y -2 dv xl
  270982. gr}for
  270983. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  270984. rev{1 -1 sc}if
  270985. 0 lW 2 m xl
  270986. D SA OA
  270987. rad 0 xl
  270988. 180 ro
  270989. 0 lW 2 m xl
  270990. SA OA}b/Aos{X Y M SM cp
  270991. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  270992. o 0 lt o 0 lt ne/rev x
  270993. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  270994. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  270995. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  270996. lp 0 p M
  270997. 0 0 0 Y lp ac
  270998. 0 Y 2 dv lp neg o lp ac
  270999. 0 Y 2 dv 0 Y lp ac
  271000. 0 Y lp Y lp ac
  271001. X lp s 0 p M
  271002. X 0 X Y lp ac
  271003. X Y 2 dv X lp a o lp ac
  271004. X Y 2 dv X Y lp ac
  271005. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  271006. s 180 pA a arc st
  271007. np X Y s Y 2 dv
  271008. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  271009. rO D rlineto
  271010. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  271011. rO lW -2 dv a Y lW 2 dv a rO a p l
  271012. lW -2 dv Y lW 2 dv a p l
  271013. 0 Y p l X Y p l X 0 p l cp f
  271014. 0 0 p M
  271015. 0 Y p l
  271016. X Y p l
  271017. X 0 p l cp
  271018. SM st}{Rr SM st}{rO Y p M rO rO xl
  271019. 0 Y X Y rO ac
  271020. X Y X 0 rO ac
  271021. X 0 0 0 rO ac
  271022. rO neg D xl X Y 0 Y rO ac
  271023. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  271024. -1 -1 sc LB whf}{Asc gs gLB gr
  271025. -0.4 -0.4
  271026.  sc LB whf}{Asc LB gs whf gr
  271027. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  271028. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  271029. gs 3.6 12 sc gOv gr
  271030. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  271031. gs 3.6 12 sc Cr whf gr
  271032. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  271033. 0 -1 p M
  271034. 0 0 1 0 1 ac
  271035. 8 0 8 1 1 ac
  271036. 8 0 16 0 1 ac
  271037. 16 0 16 -1 1 ac
  271038. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  271039. 2 dv D sc
  271040. 1 0 M -1 0 l
  271041. 0 1 M 0 -1 l
  271042. t}{XY D X Y dt 0 0 M SM cpt xl
  271043. 2 dv D sc
  271044. 1 0 M -1 0 l
  271045. Ast}{4.5 Aos
  271046. 1 0 M -1 0 l
  271047. 0 1 M 0 -1 l
  271048. 2 0 M 0 0 2 0 360 arc
  271049. Ast}{4.5 Aos
  271050. 1 0 M -1 0 l
  271051. 2 0 M 0 0 2 0 360 arc
  271052. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  271053. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  271054. 1 -1 M -1 -1 l
  271055. 0 2 M 0 -2 l
  271056. Ast}{5 Aos
  271057. 1 -1 M -1 -1 l
  271058. 1 1 M -1 1 l
  271059. 0 2 M 0 -2 l
  271060. Ast}{4.5 Aos
  271061. 1 0 M -1 0 l
  271062. 0 1 M 0 -1 l
  271063. Ast}{4.5 Aos
  271064. 1 0 M -1 0 l
  271065. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  271066.  DLB gs whf gr
  271067. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  271068. gs 3.6 12 sc Cr whf gr
  271069. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  271070. gs 3.6 12 sc Cr blf gr
  271071. ZLB whf}{Asc LB gs whf gr
  271072. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  271073. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  271074. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  271075. e 2 ix a}b
  271076. /PT{D 2 4 gi al P OP D 1 sc
  271077. o length 6 gt{P 6 g}{e P 8 dv}ie
  271078. D lW 2 m lt{P lW 2 m}if
  271079. 0 e p
  271080. 0 0 p
  271081. 3 -1 r s 3 1 r e s e
  271082. 0 0 p M 1 0 p l
  271083. 0 0 p ap M 1 0 p ap l
  271084. e n e n
  271085. 0 0 p ap M 1 0 p ap l
  271086. P P}b
  271087. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  271088. cvi D 0 eq{P 1}if/nH x
  271089. D hS nH m s
  271090. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  271091. bW 2 dv/bd x
  271092. lW 2 dv e D NH e{D bd p M bd n p l}for
  271093. st gr}{gs 12 OB np
  271094. lW 2 dv 0 xl NH 1 sc
  271095. bW 2 dv wF m
  271096.  nH 1 a dv/bd x
  271097. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  271098. np 0 lW 2 dv o o n p M p l bW 2 dv
  271099. wF m o o p l n p l
  271100. cp f gr}{P}{gs 12 OB/bL x
  271101. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  271102. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  271103. bL nSq 2 m dv D sc
  271104. nSq{.135  .667 .865  .667 1 0 rcurveto
  271105. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  271106. np 0 lW 2 dv o o n p M p l bW 2 dv
  271107. wF m o o p l n p l
  271108. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  271109. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  271110. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  271111. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  271112. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  271113. 5 -1 r dv neg e 5 -1 r dv neg e
  271114. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  271115. %%EndProcSet
  271116. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  271117. 3510 1340 155 540 
  271118. SPn/origstk x
  271119. 65535 65535 65535 sBg
  271120. 0 0 0 C
  271121. 1950 4204 M
  271122. 1970 4216 l
  271123. 1445 4519 l
  271124. 1435 4501 l
  271125. 1950 3616 M
  271126. 1970 3604 l
  271127. 1970 4216 l
  271128. 1950 4204 l
  271129. 1440 3322 M
  271130. 1440 3310 l
  271131. 1450 3304 l
  271132. 1970 3604 l
  271133. 1950 3616 l
  271134. 1430 3304 M
  271135. 1440 3310 l
  271136. 1440 3322 l
  271137. 925 3619 l
  271138. 915 3601 l
  271139. 960 3610 1200 4060 36 Ar
  271140. 1450 3304 M
  271141. 1440 3310 l
  271142. 1430 3304 l
  271143. 1430 2822 l
  271144. 1450 2822 l
  271145. 1522 3268 M
  271146. 1502 3268 l
  271147. 1502 2822 l
  271148. 1522 2822 l
  271149. f[1 9 1526 2613 1752 2361 ]Bd
  271150. 5200 3550 3280 3550 2 Ar
  271151. 7410 4374 M
  271152. 7430 4386 l
  271153. 6905 4689 l
  271154. 6895 4671 l
  271155. 7410 3786 M
  271156. 7430 3774 l
  271157. 7430 4386 l
  271158. 7410 4374 l
  271159. 6900 3492 M
  271160. 6900 3480 l
  271161. 6910 3474 l
  271162. 7430 3774 l
  271163. 7410 3786 l
  271164. 6890 3474 M
  271165. 6900 3480 l
  271166. 6900 3492 l
  271167. 6385 3789 l
  271168. 6375 3771 l
  271169. 6420 3780 6660 4230 36 Ar
  271170. 6910 3474 M
  271171. 6900 3480 l
  271172. 6890 3474 l
  271173. 6890 2994 l
  271174. 6910 2994 l
  271175. 6982 3438 M
  271176. 6962 3438 l
  271177. 6962 2994 l
  271178. 6982 2994 l
  271179. f[1 9 6986 2784 7211 2532 ]Bd
  271180. 9920 3550 7860 3550 2 Ar
  271181. 11890 4434 M
  271182. 11910 4446 l
  271183. 11385 4749 l
  271184. 11375 4731 l
  271185. 11890 3846 M
  271186. 11910 3834 l
  271187. 11910 4446 l
  271188. 11890 4434 l
  271189. 11380 3552 M
  271190. 11380 3540 l
  271191. 11390 3534 l
  271192. 11910 3834 l
  271193. 11890 3846 l
  271194. 11375 3632 M
  271195. 11385 3614 l
  271196. 11833 3873 l
  271197. 11823 3891 l
  271198. 11370 3534 M
  271199. 11380 3540 l
  271200. 11380 3552 l
  271201. 10865 3849 l
  271202. 10855 3831 l
  271203. 10900 3840 11140 4290 36 Ar
  271204. 11390 3534 M
  271205. 11380 3540 l
  271206. 11370 3534 l
  271207. 11370 3054 l
  271208. 11390 3054 l
  271209. 11685 2585 M
  271210. 11699 2599 l
  271211. 11473 2851 l
  271212. 11459 2837 l
  271213. 11739 2633 M
  271214. 11753 2647 l
  271215. 11527 2899 l
  271216. 11513
  271217.  2885 l
  271218. 14600 3650 12580 3650 2 Ar
  271219. 2060 7084 M
  271220. 2080 7096 l
  271221. 1555 7399 l
  271222. 1545 7381 l
  271223. 2060 6496 M
  271224. 2080 6484 l
  271225. 2080 7096 l
  271226. 2060 7084 l
  271227. 1988 6532 M
  271228. 2008 6532 l
  271229. 2008 7048 l
  271230. 1988 7048 l
  271231. 1550 6202 M
  271232. 1550 6190 l
  271233. 1560 6184 l
  271234. 2080 6484 l
  271235. 2060 6496 l
  271236. 1540 6184 M
  271237. 1550 6190 l
  271238. 1550 6202 l
  271239. 1035 6499 l
  271240. 1025 6481 l
  271241. 1070 6490 1310 6940 36 Ar
  271242. 1560 6184 M
  271243. 1550 6190 l
  271244. 1540 6184 l
  271245. 1540 5702 l
  271246. 1560 5702 l
  271247. 1632 6148 M
  271248. 1612 6148 l
  271249. 1612 5702 l
  271250. 1632 5702 l
  271251. 1856 5233 M
  271252. 1870 5247 l
  271253. 1645 5499 l
  271254. 1631 5485 l
  271255. 4920 6620 3000 6620 2 Ar
  271256. 6900 7064 M
  271257. 6920 7076 l
  271258. 6395 7379 l
  271259. 6385 7361 l
  271260. 6900 6476 M
  271261. 6920 6464 l
  271262. 6920 7076 l
  271263. 6900 7064 l
  271264. 6828 6512 M
  271265. 6848 6512 l
  271266. 6848 7028 l
  271267. 6828 7028 l
  271268. 6380 6176 M
  271269. 6400 6164 l
  271270. 6920 6464 l
  271271. 6900 6476 l
  271272. 6385 6120 M
  271273. 6395 6138 l
  271274. 5857 6448 l
  271275. 5847 6430 l
  271276. 6420 6181 M
  271277. 6430 6199 l
  271278. 5893 6510 l
  271279. 5883 6492 l
  271280. 5910 6470 6150 6920 36 Ar
  271281. 6400 6164 M
  271282. 6380 6176 l
  271283. 6380 5684 l
  271284. 6400 568
  271285. 9600 6580 7640 6580 2 Ar
  271286. 11370 7054 M
  271287. 11390 7066 l
  271288. 10865 7369 l
  271289. 10855 7351 l
  271290. 11370 6466 M
  271291. 11390 6454 l
  271292. 11390 7066 l
  271293. 11370 7054 l
  271294. 11298 6502 M
  271295. 11318 6502 l
  271296. 11318 7018 l
  271297. 11298 7018 l
  271298. 10850 6166 M
  271299. 10870 6154 l
  271300. 11390 6454 l
  271301. 11370 6466 l
  271302. 10855 6110 M
  271303. 10865 6128 l
  271304. 10327 6438 l
  271305. 10317 6420 l
  271306. 10890 6171 M
  271307. 10900 6189 l
  271308. 10363 6500 l
  271309. 10353 6482 l
  271310. 10380 6460 10620 6910 36 Ar
  271311. 10870 6154 M
  271312. 10850 6166 l
  271313. 10850 5674 l
  271314. 10870 5674 l
  271315. count o
  271316. rigstk sub{P}rp end
  271317. chemsave restore
  271318.     Helvetica
  271319. N(Ts)
  271320. Times
  271321. DMF / NaH / 0
  271322. C -> 25
  271323. p-TsCl
  271324. ClC6H6
  271325. H    1) n-Bu
  271326. C -> 25
  271327. N(Ts)2
  271328. DMF / NaH / 0oC -> 25oC
  271329. p-TsCl
  271330. ClC6H6
  271331.     1) n-BuLi
  271332. -60oC -> 25oC
  271333.     Helvetica
  271334. Times
  271335. Untitled preferences-1
  271336. count
  271337. currentpoint 192837465
  271338. currentpoint
  271339. save/chemsave exch def
  271340. %%BeginProcSet: chemdict30 24 10
  271341. % ChemDraw Laser Prep
  271342. % Copyright 198
  271343. 1993, Cambridge Scientific Computing, Inc.
  271344. userdict/chemdict30 210 dict put
  271345. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  271346. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/pop
  271347.  L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  271348. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  271349. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/sf
  271350.  20 d/cW 20 d/lW 20 d/bW 75 d/wF
  271351. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  271352. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  271353. x}b/sRm
  271354. p{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  271355. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  271356. 0 cw 2 dv xl
  271357. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  271358. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  271359. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  271360. St 16 and 0 ne{2 ix
  271361.  6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  271362. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  271363. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  271364. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  271365. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  271366. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  271367. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 aA 
  271368. a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
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  271370. P P}{sq at 2
  271371. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  271372. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  271373. l w .35
  271374.  dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  271375. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  271376. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  271377. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA O
  271378. A}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  271379. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  271380. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  271381. 21 -10 27 -8 27 0 cv
  271382. 27 8 21 10 9 6 cv
  271383. -3 2 -3 -2 9 -6 cv
  271384. cp}b/DLB{0 0 M -4.8 4.8 l
  271385. -8 8 -9.6 12 -9.6 16.8 cv
  271386. -9.6 21.6
  271387.  -8 24.6 -4.8 25.8 cv
  271388. -1.6 27 1.6 27 4.8 25.8 cv
  271389. 8 24.6 9.6 21.6 9.6 16.8 cv
  271390. 9.6 12 8 8 4.8 4.8 cv
  271391. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  271392. 0 Y X Y rO ac
  271393. X Y X 0 rO ac
  271394. X 0 0 0 rO ac
  271395. 0 0 0 Y rO ac
  271396. cp}b/Rc{0 0 p M
  271397. 0 Y p l
  271398. X Y p l
  271399. X 0 p l
  271400. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  271401. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT idt
  271402. ransform
  271403. m D 0 lt{n}if sq n D
  271404. CMT dtransform idtransform
  271405. e 2 m e
  271406. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  271407. 32 -0.5 0.5{gs
  271408. 13.5 0 xl
  271409. D 32 s 64 dv 13.5 m D 7 m 24 dv
  271410. -13.5 0 xl
  271411. gr}for
  271412. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  271413. 32 -0.5 0.5{gs
  271414. D 32 s 64 dv 0.65 m D
  271415. gr}for
  271416. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  271417. 32 -0.5 0.5{gs
  271418. D 32 s 64 dv D
  271419. gr}for
  271420. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  271421. 32 -0.5 0.5{gs
  271422. 0 13.5 xl
  271423. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  271424. 0 -13.5 xl
  271425. DLB f
  271426. gr}for
  271427. DLB SM st}
  271428. {DLB grf}ie}b/gRr{sh{sRmp
  271429. 32 -0.5 0.5{gs
  271430. X 2 dv Y 2 dv xl
  271431. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  271432. X -2 dv Y -2 dv xl
  271433. gr}for
  271434. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  271435. 32 -0.5 0.5{gs
  271436. X 2 dv Y 2 dv xl
  271437. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  271438. X -2 dv Y -2 dv xl
  271439. gr}for
  271440. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  271441. rev{1 -1 sc}if
  271442. 0 lW 2 m xl
  271443. D SA OA
  271444. rad 0 xl
  271445. 180 ro
  271446. 0 lW 2 m xl
  271447. SA OA}b/Aos{X Y M SM cp
  271448. t xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  271449. o 0 lt o 0 lt ne/rev x
  271450. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  271451. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  271452. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  271453. lp 0 p M
  271454. 0 0 0 Y lp ac
  271455. 0 Y 2 dv lp neg o lp ac
  271456. 0 Y 2 dv 0 Y lp ac
  271457. 0 Y lp Y lp ac
  271458. X lp s 0 p M
  271459. X 0 X Y lp ac
  271460. X Y 2 dv X lp a o lp ac
  271461. X Y 2 dv X Y lp ac
  271462. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 pA 
  271463. s 180 pA a arc st
  271464. np X Y s Y 2 dv
  271465. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  271466. rO D rlineto
  271467. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  271468. rO lW -2 dv a Y lW 2 dv a rO a p l
  271469. lW -2 dv Y lW 2 dv a p l
  271470. 0 Y p l X Y p l X 0 p l cp f
  271471. 0 0 p M
  271472. 0 Y p l
  271473. X Y p l
  271474. X 0 p l cp
  271475. SM st}{Rr SM st}{rO Y p M rO rO xl
  271476. 0 Y X Y rO ac
  271477. X Y X 0 rO ac
  271478. X 0 0 0 rO ac
  271479. rO neg D xl X Y 0 Y rO ac
  271480. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  271481. -1 -1 sc LB whf}{Asc gs gLB gr
  271482. -0.4 -0.4
  271483.  sc LB whf}{Asc LB gs whf gr
  271484. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  271485. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  271486. gs 3.6 12 sc gOv gr
  271487. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  271488. gs 3.6 12 sc Cr whf gr
  271489. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  271490. 0 -1 p M
  271491. 0 0 1 0 1 ac
  271492. 8 0 8 1 1 ac
  271493. 8 0 16 0 1 ac
  271494. 16 0 16 -1 1 ac
  271495. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  271496. 2 dv D sc
  271497. 1 0 M -1 0 l
  271498. 0 1 M 0 -1 l
  271499. t}{XY D X Y dt 0 0 M SM cpt xl
  271500. 2 dv D sc
  271501. 1 0 M -1 0 l
  271502. Ast}{4.5 Aos
  271503. 1 0 M -1 0 l
  271504. 0 1 M 0 -1 l
  271505. 2 0 M 0 0 2 0 360 arc
  271506. Ast}{4.5 Aos
  271507. 1 0 M -1 0 l
  271508. 2 0 M 0 0 2 0 360 arc
  271509. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  271510. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  271511. 1 -1 M -1 -1 l
  271512. 0 2 M 0 -2 l
  271513. Ast}{5 Aos
  271514. 1 -1 M -1 -1 l
  271515. 1 1 M -1 1 l
  271516. 0 2 M 0 -2 l
  271517. Ast}{4.5 Aos
  271518. 1 0 M -1 0 l
  271519. 0 1 M 0 -1 l
  271520. Ast}{4.5 Aos
  271521. 1 0 M -1 0 l
  271522. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 sc
  271523.  DLB gs whf gr
  271524. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  271525. gs 3.6 12 sc Cr whf gr
  271526. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  271527. gs 3.6 12 sc Cr blf gr
  271528. ZLB whf}{Asc LB gs whf gr
  271529. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  271530. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  271531. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  271532. e 2 ix a}b
  271533. /PT{D 2 4 gi al P OP D 1 sc
  271534. o length 6 gt{P 6 g}{e P 8 dv}ie
  271535. D lW 2 m lt{P lW 2 m}if
  271536. 0 e p
  271537. 0 0 p
  271538. 3 -1 r s 3 1 r e s e
  271539. 0 0 p M 1 0 p l
  271540. 0 0 p ap M 1 0 p ap l
  271541. e n e n
  271542. 0 0 p ap M 1 0 p ap l
  271543. P P}b
  271544. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  271545. cvi D 0 eq{P 1}if/nH x
  271546. D hS nH m s
  271547. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  271548. bW 2 dv/bd x
  271549. lW 2 dv e D NH e{D bd p M bd n p l}for
  271550. st gr}{gs 12 OB np
  271551. lW 2 dv 0 xl NH 1 sc
  271552. bW 2 dv wF m
  271553.  nH 1 a dv/bd x
  271554. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  271555. np 0 lW 2 dv o o n p M p l bW 2 dv
  271556. wF m o o p l n p l
  271557. cp f gr}{P}{gs 12 OB/bL x
  271558. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  271559. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  271560. bL nSq 2 m dv D sc
  271561. nSq{.135  .667 .865  .667 1 0 rcurveto
  271562. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  271563. np 0 lW 2 dv o o n p M p l bW 2 dv
  271564. wF m o o p l n p l
  271565. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi al 
  271566. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  271567. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  271568. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  271569. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  271570. 5 -1 r dv neg e 5 -1 r dv neg e
  271571. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  271572. %%EndProcSet
  271573. 40 80 20 4 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  271574. 2475 595 603 683 SPn/origstk x
  271575. 65535 65535 65535 sBg
  271576. 0 0 0 C
  271577. 5110 4030 3770 4030 2 Ar
  271578. 10130 4110 8350 4110 2 Ar
  271579. 2500 4404 M
  271580. 2480 4416 l
  271581. 2480 3804 l
  271582. 2500 3816 l
  271583. 3010 4698 M
  271584. 3010 4722 l
  271585. 2480 4416 l
  271586. 2500 4404 l
  271587. 3520 4404 M
  271588. 3540 4416 l
  271589. 3010 4722 l
  271590. 3010 4698 l
  271591. 3520 3816 M
  271592. 3540 3804 l
  271593. 3540 4416 l
  271594. 3520 4404 l
  271595. 3448 3852 M
  271596. 3468 3852 l
  271597. 3468 4368 l
  271598. 3448 4368 l
  271599. 3010 3522 M
  271600. 3010 3498 l
  271601. 3540 3804 l
  271602. 3520 3816 l
  271603. 3010 3498 M
  271604. 3010 3522 l
  271605. 2500 3816 l
  271606. 2480 3804 l
  271607. 2964 3026 M
  271608. 2984 3026 l
  271609. 2984 3530 l
  271610. 2964 3530 l
  271611. 3036 3026 M
  271612. 3056 3026 l
  271613. 3056 3530 l
  271614. 3036 3530 l
  271615. 6190 4654 M
  271616. 70 4666 l
  271617. 6170 4054 l
  271618. 6190 4066 l
  271619. 6700 4948 M
  271620. 6700 4972 l
  271621. 6170 4666 l
  271622. 6190 4654 l
  271623. 7210 4654 M
  271624. 7220 4660 l
  271625. 7221 4672 l
  271626. 6700 4972 l
  271627. 6700 4948 l
  271628. 7210 4066 M
  271629. 7230 4054 l
  271630. 7230 4655 l
  271631. 7220 4660 l
  271632. 7210 4654 l
  271633. 6700 3772 M
  271634. 6700 3760 l
  271635. 6710 3754 l
  271636. 7230 4054 l
  271637. 7210 4066 l
  271638. 6695 3852 M
  271639. 6705 3834 l
  271640. 7153 4093 l
  271641. 7143 4111 l
  271642. 6690 3754 M
  271643. 6700 3760 l
  271644. 6700 3772 l
  271645. 6190 4066 l
  271646. 6170 4054 l
  271647. 6690 3278 M
  271648. 6710 3278 l
  271649. 6710 3754 l
  271650. 6700 3760 l
  271651. 6690 3754 l
  271652. 7624 4906 M
  271653. 7614 4922 l
  271654. 7221 4672 l
  271655. 7220 4660 l
  271656. 7230 4655 l
  271657. 7099 2885 M
  271658. 7111 2901 l
  271659. 6814 3097 l
  271660. 6802 3081 l
  271661. 10670 4594 M
  271662. 10650 4606 l
  271663. 10650 3994 l
  271664. 10670 4006 l
  271665. 11180 4888 M
  271666. 11180 4912 l
  271667. 10650 4606 l
  271668. 10670 4594 l
  271669. 11690 4594 M
  271670. 11700 4600 l
  271671. 11700 4612 l
  271672. 11180 4912 l
  271673. 11180 4888 l
  271674. 11690 4006 M
  271675. 11710 3994 l
  271676. 11710 4594 l
  271677. 11700 4600 l
  271678. 11690 4594 l
  271679. 11618 4042 M
  271680. 11638 4042 l
  271681. 11638 4558 l
  271682. 11618 4558 l
  271683. 11180 3712 M
  271684. 11180 3688 l
  271685. 11710 3994 l
  271686. 11690
  271687.  4006 l
  271688. 11180 3688 M
  271689. 11180 3712 l
  271690. 10670 4006 l
  271691. 10650 3994 l
  271692. 11134 3218 M
  271693. 11154 3218 l
  271694. 11154 3720 l
  271695. 11134 3720 l
  271696. 11206 3218 M
  271697. 11226 3218 l
  271698. 11226 3720 l
  271699. 11206 3720 l
  271700. 12124 4848 M
  271701. 12114 4866 l
  271702. 11700 4612 l
  271703. 11700 4600 l
  271704. 11710 4594 l
  271705. count origstk sub{P}rp end
  271706. chemsave restore
  271707. Times
  271708. BtSiMe
  271709. A    1) LDA, E
  271710.     Helvetica
  271711. ,CHMD
  271712. SiMe3
  271713. BtSiMe3
  271714. 1) LDA, E+
  271715. 2) H3O+
  271716.     Helvetica
  271717. Times
  271718. Untitled preferences-2
  271719. count
  271720. currentpoint 192837465
  271721. currentpoint
  271722. save/chemsave exch def
  271723. %%BeginProcSet: chemdict30 24 10
  271724. % ChemDraw Laser Prep
  271725. % Copyright 198
  271726. 6-1993, Cambridge Scientific Computing, Inc.
  271727. userdict/chemdict30 210 dict put
  271728. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  271729. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  271730. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  271731. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  271732. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  271733. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  271734. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  271735. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  271736. x}b/s
  271737. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  271738. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  271739. 0 cw 2 dv xl
  271740. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  271741. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  271742. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  271743. St 16 and 0 ne{2 
  271744. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  271745. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  271746. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  271747. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  271748. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  271749. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  271750. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  271751. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  271752. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  271753. P P}{sq at 2
  271754. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  271755. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  271756. l w .
  271757. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  271758. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  271759. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  271760. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  271761.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  271762. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  271763. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  271764. 21 -10 27 -8 27 0 cv
  271765. 27 8 21 10 9 6 cv
  271766. -3 2 -3 -2 9 -6 cv
  271767. cp}b/DLB{0 0 M -4.8 4.8 l
  271768. -8 8 -9.6 12 -9.6 16.8 cv
  271769. -9.6 21
  271770. .6 -8 24.6 -4.8 25.8 cv
  271771. -1.6 27 1.6 27 4.8 25.8 cv
  271772. 8 24.6 9.6 21.6 9.6 16.8 cv
  271773. 9.6 12 8 8 4.8 4.8 cv
  271774. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  271775. 0 Y X Y rO ac
  271776. X Y X 0 rO ac
  271777. X 0 0 0 rO ac
  271778. 0 0 0 Y rO ac
  271779. cp}b/Rc{0 0 p M
  271780. 0 Y p l
  271781. X Y p l
  271782. X 0 p l
  271783. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  271784. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  271785. dtransform
  271786. m D 0 lt{n}if sq n D
  271787. CMT dtransform idtransform
  271788. e 2 m e
  271789. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  271790. 32 -0.5 0.5{gs
  271791. 13.5 0 xl
  271792. D 32 s 64 dv 13.5 m D 7 m 24 dv
  271793. -13.5 0 xl
  271794. gr}for
  271795. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  271796. 32 -0.5 0.5{gs
  271797. D 32 s 64 dv 0.65 m D
  271798. gr}for
  271799. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  271800. 32 -0.5 0.5{gs
  271801. D 32 s 64 dv D
  271802. gr}for
  271803. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  271804. 32 -0.5 0.5{gs
  271805. 0 13.5 xl
  271806. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  271807. 0 -13.5 xl
  271808. DLB f
  271809. gr}for
  271810. DLB SM s
  271811. t}{DLB grf}ie}b/gRr{sh{sRmp
  271812. 32 -0.5 0.5{gs
  271813. X 2 dv Y 2 dv xl
  271814. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  271815. X -2 dv Y -2 dv xl
  271816. gr}for
  271817. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  271818. 32 -0.5 0.5{gs
  271819. X 2 dv Y 2 dv xl
  271820. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  271821. X -2 dv Y -2 dv xl
  271822. gr}for
  271823. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  271824. rev{1 -1 sc}if
  271825. 0 lW 2 m xl
  271826. D SA OA
  271827. rad 0 xl
  271828. 180 ro
  271829. 0 lW 2 m xl
  271830. SA OA}b/Aos{X Y M SM 
  271831. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  271832. o 0 lt o 0 lt ne/rev x
  271833. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  271834. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  271835. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  271836. lp 0 p M
  271837. 0 0 0 Y lp ac
  271838. 0 Y 2 dv lp neg o lp ac
  271839. 0 Y 2 dv 0 Y lp ac
  271840. 0 Y lp Y lp ac
  271841. X lp s 0 p M
  271842. X 0 X Y lp ac
  271843. X Y 2 dv X lp a o lp ac
  271844. X Y 2 dv X Y lp ac
  271845. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  271846. A s 180 pA a arc st
  271847. np X Y s Y 2 dv
  271848. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  271849. rO D rlineto
  271850. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  271851. rO lW -2 dv a Y lW 2 dv a rO a p l
  271852. lW -2 dv Y lW 2 dv a p l
  271853. 0 Y p l X Y p l X 0 p l cp f
  271854. 0 0 p M
  271855. 0 Y p l
  271856. X Y p l
  271857. X 0 p l cp
  271858. SM st}{Rr SM st}{rO Y p M rO rO xl
  271859. 0 Y X Y rO ac
  271860. X Y X 0 rO ac
  271861. X 0 0 0 rO ac
  271862. rO neg D xl X Y 0 Y rO ac
  271863. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  271864. -1 -1 sc LB whf}{Asc gs gLB gr
  271865. -0.4 -0
  271866. .4 sc LB whf}{Asc LB gs whf gr
  271867. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  271868. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  271869. gs 3.6 12 sc gOv gr
  271870. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  271871. gs 3.6 12 sc Cr whf gr
  271872. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  271873. 0 -1 p M
  271874. 0 0 1 0 1 ac
  271875. 8 0 8 1 1 ac
  271876. 8 0 16 0 1 ac
  271877. 16 0 16 -1 1 ac
  271878. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  271879. 2 dv D sc
  271880. 1 0 M -1 0 l
  271881. 0 1 M 0 -1 l
  271882. Ast}{XY D X Y dt 0 0 M SM cpt xl
  271883. 2 dv D sc
  271884. 1 0 M -1 0 l
  271885. Ast}{4.5 Aos
  271886. 1 0 M -1 0 l
  271887. 0 1 M 0 -1 l
  271888. 2 0 M 0 0 2 0 360 arc
  271889. Ast}{4.5 Aos
  271890. 1 0 M -1 0 l
  271891. 2 0 M 0 0 2 0 360 arc
  271892. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  271893. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  271894. 1 -1 M -1 -1 l
  271895. 0 2 M 0 -2 l
  271896. Ast}{5 Aos
  271897. 1 -1 M -1 -1 l
  271898. 1 1 M -1 1 l
  271899. 0 2 M 0 -2 l
  271900. Ast}{4.5 Aos
  271901. 1 0 M -1 0 l
  271902. 0 1 M 0 -1 l
  271903. Ast}{4.5 Aos
  271904. 1 0 M -1 0 l
  271905. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  271906. sc DLB gs whf gr
  271907. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  271908. gs 3.6 12 sc Cr whf gr
  271909. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  271910. gs 3.6 12 sc Cr blf gr
  271911. ZLB whf}{Asc LB gs whf gr
  271912. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  271913. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  271914. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  271915. e 2 ix a
  271916. }b/PT{D 2 4 gi al P OP D 1 sc
  271917. o length 6 gt{P 6 g}{e P 8 dv}ie
  271918. D lW 2 m lt{P lW 2 m}if
  271919. 0 e p
  271920. 0 0 p
  271921. 3 -1 r s 3 1 r e s e
  271922. 0 0 p M 1 0 p l
  271923. 0 0 p ap M 1 0 p ap l
  271924. e n e n
  271925. 0 0 p ap M 1 0 p ap l
  271926. P P}b
  271927. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  271928. cvi D 0 eq{P 1}if/nH x
  271929. D hS nH m s
  271930. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  271931. bW 2 dv/bd x
  271932. lW 2 dv e D NH e{D bd p M bd n p l}for
  271933. st gr}{gs 12 OB np
  271934. lW 2 dv 0 xl NH 1 sc
  271935. bW 2 dv wF
  271936.  m nH 1 a dv/bd x
  271937. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  271938. np 0 lW 2 dv o o n p M p l bW 2 dv
  271939. wF m o o p l n p l
  271940. cp f gr}{P}{gs 12 OB/bL x
  271941. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  271942. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  271943. bL nSq 2 m dv D sc
  271944. nSq{.135  .667 .865  .667 1 0 rcurveto
  271945. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  271946. np 0 lW 2 dv o o n p M p l bW 2 dv
  271947. wF m o o p l n p l
  271948. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  271949. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  271950. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  271951. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  271952. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  271953. 5 -1 r dv neg e 5 -1 r dv neg e
  271954. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  271955. %%EndProcSet
  271956. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  271957. 349 119 58 30 SPn/origstk x
  271958. 65535 65535 65535 sBg
  271959. 0 0 0 C
  271960. 2239 2364 M
  271961. 2259 2380 l
  271962. 1887 2480 l
  271963. 1881 2460 l
  271964. 2239 1912 M
  271965. 2259 1924 l
  271966. 2259 2380 l
  271967. 2239 2364 l
  271968. 2503 2574 M
  271969. 2489 2588 l
  271970. 2242 2341 l
  271971. 2256 2327 l
  271972. 2465 2612 M
  271973. 2451 2626 l
  271974. 2213 2387 l
  271975. 2227 2373 l
  271976. 2642 1679 M
  271977. 2642 1703 l
  271978. 2259 1924 l
  271979. 2239 1912 l
  271980. 3035 1906 M
  271981. 3035 1918 l
  271982. 3007 1914 l
  271983. 2642 1703 l
  271984. 2642 1679 l
  271985. 3418 1685 M
  271986. 3438 1697 l
  271987. 3063 1914 l
  271988. 3035 1918 l
  271989. 3035 1906 l
  271990. f[1 3 2642 1635 2642 1350 ]Bd
  271991. 3418 1350 M
  271992. 3438 1350 l
  271993. 3438 1697 l
  271994. 3418 1685 l
  271995. 3019 1008 M
  271996. 3035 1010 l
  271997. 3035 1022 l
  271998. 2755 1184 l
  271999. 2745 1166 l
  272000. 3035 1022 M
  272001. 3035 1010 l
  272002. 3051 1008 l
  272003. 3315 1160 l
  272004. 3305 1178 l
  272005. 2838 827 M
  272006. 2852 813 l
  272007. 3035 996 l
  272008. 3035 1010 l
  272009. 3019 1008 l
  272010. 3244 787 M
  272011. 3258 801 l
  272012. 3051 1008 l
  272013. 3035 1010 l
  272014. 3035 996 l
  272015. 3063 23
  272016. 3007 2368 l
  272017. 3007 1914 l
  272018. 3035 1918 l
  272019. 3063 1914 l
  272020. 3433 2590 M
  272021. 3423 2608 l
  272022. 3007 2368 l
  272023. 3063 2376 l
  272024. 5610 1791 3990 1791 2 Ar
  272025. 7212 1809 M
  272026. 7212 1833 l
  272027. 6831 2053 l
  272028. 6807 2043 l
  272029. 7605 2036 M
  272030. 7605 2048 l
  272031. 7593 2053 l
  272032. 7212 1833 l
  272033. 7212 1809 l
  272034. 7988 1815 M
  272035. 8008 1827 l
  272036. 7614 2055 l
  272037. 7605 2048 l
  272038. 7605 2036 l
  272039. f[1 3 7212 1771 7212 1470 ]Bd
  272040. 7988 1470 M
  272041. 8008 1470 l
  272042. 8008 1827 l
  272043. 7988 1815 l
  272044. 7589 1138 M
  272045. 7605 1140 l
  272046. 7605 1152 l
  272047. 7315 1320 l
  272048. 7305 1302 l
  272049. 7605 1
  272050. 152 M
  272051. 7605 1140 l
  272052. 7621 1138 l
  272053. 7875 1284 l
  272054. 7865 1302 l
  272055. 7418 967 M
  272056. 7432 953 l
  272057. 7605 1126 l
  272058. 7605 1140 l
  272059. 7589 1138 l
  272060. 7814 917 M
  272061. 7828 931 l
  272062. 7621 1138 l
  272063. 7605 1140 l
  272064. 7605 1126 l
  272065. 7593 2053 M
  272066. 7605 2048 l
  272067. 7614 2055 l
  272068. 7496 2497 l
  272069. 7480 2477 l
  272070. 6807 2043 M
  272071. 6831 2053 l
  272072. 6945 2477 l
  272073. 6937 2487 l
  272074. 6920 2464 l
  272075. 7480 2477 M
  272076. 7496 2497 l
  272077. 6967 2497 l
  272078. 6937 2487 l
  272079. 6945 2477 l
  272080. f[1 3 7698 2697 7523 2522 ]Bd
  272081. 6704 2760 M
  272082. 6664 2720 l
  272083. 6920 2464 l
  272084. 6937 2487 l
  272085. 6967 2497 l
  272086. 3 7651 2075 7884 2210 ]Bd
  272087. count origstk sub{P}rp end
  272088. chemsave restore
  272089.     Helvetica
  272090. Palatino
  272091. (Oct)
  272092. DCM, rt
  272093. MeO2C
  272094. MeO2C
  272095.     Rh2(Oct)4
  272096. DCM, rt?
  272097.     Helvetica
  272098. Palatinoa
  272099. Untitled preferences-3
  272100. count
  272101. currentpoint 192837465
  272102. currentpoint
  272103. save/chemsave exch def
  272104. %%BeginProcSet: chemdict30 24 10
  272105. % ChemDraw Laser Prep
  272106. % Copyright 198
  272107. 6-1993, Cambridge Scientific Computing, Inc.
  272108. userdict/chemdict30 210 dict put
  272109. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  272110. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  272111. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  272112. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  272113. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  272114. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  272115. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  272116. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  272117. x}b/s
  272118. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272119. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272120. 0 cw 2 dv xl
  272121. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  272122. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  272123. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  272124. St 16 and 0 ne{2 
  272125. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  272126. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  272127. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  272128. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  272129. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  272130. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  272131. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  272132. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  272133. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  272134. P P}{sq at 2
  272135. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  272136. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  272137. l w .
  272138. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  272139. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  272140. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  272141. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  272142.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  272143. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  272144. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  272145. 21 -10 27 -8 27 0 cv
  272146. 27 8 21 10 9 6 cv
  272147. -3 2 -3 -2 9 -6 cv
  272148. cp}b/DLB{0 0 M -4.8 4.8 l
  272149. -8 8 -9.6 12 -9.6 16.8 cv
  272150. -9.6 21
  272151. .6 -8 24.6 -4.8 25.8 cv
  272152. -1.6 27 1.6 27 4.8 25.8 cv
  272153. 8 24.6 9.6 21.6 9.6 16.8 cv
  272154. 9.6 12 8 8 4.8 4.8 cv
  272155. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  272156. 0 Y X Y rO ac
  272157. X Y X 0 rO ac
  272158. X 0 0 0 rO ac
  272159. 0 0 0 Y rO ac
  272160. cp}b/Rc{0 0 p M
  272161. 0 Y p l
  272162. X Y p l
  272163. X 0 p l
  272164. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  272165. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  272166. dtransform
  272167. m D 0 lt{n}if sq n D
  272168. CMT dtransform idtransform
  272169. e 2 m e
  272170. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  272171. 32 -0.5 0.5{gs
  272172. 13.5 0 xl
  272173. D 32 s 64 dv 13.5 m D 7 m 24 dv
  272174. -13.5 0 xl
  272175. gr}for
  272176. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  272177. 32 -0.5 0.5{gs
  272178. D 32 s 64 dv 0.65 m D
  272179. gr}for
  272180. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  272181. 32 -0.5 0.5{gs
  272182. D 32 s 64 dv D
  272183. gr}for
  272184. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  272185. 32 -0.5 0.5{gs
  272186. 0 13.5 xl
  272187. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  272188. 0 -13.5 xl
  272189. DLB f
  272190. gr}for
  272191. DLB SM s
  272192. t}{DLB grf}ie}b/gRr{sh{sRmp
  272193. 32 -0.5 0.5{gs
  272194. X 2 dv Y 2 dv xl
  272195. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  272196. X -2 dv Y -2 dv xl
  272197. gr}for
  272198. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  272199. 32 -0.5 0.5{gs
  272200. X 2 dv Y 2 dv xl
  272201. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  272202. X -2 dv Y -2 dv xl
  272203. gr}for
  272204. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  272205. rev{1 -1 sc}if
  272206. 0 lW 2 m xl
  272207. D SA OA
  272208. rad 0 xl
  272209. 180 ro
  272210. 0 lW 2 m xl
  272211. SA OA}b/Aos{X Y M SM 
  272212. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  272213. o 0 lt o 0 lt ne/rev x
  272214. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  272215. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  272216. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  272217. lp 0 p M
  272218. 0 0 0 Y lp ac
  272219. 0 Y 2 dv lp neg o lp ac
  272220. 0 Y 2 dv 0 Y lp ac
  272221. 0 Y lp Y lp ac
  272222. X lp s 0 p M
  272223. X 0 X Y lp ac
  272224. X Y 2 dv X lp a o lp ac
  272225. X Y 2 dv X Y lp ac
  272226. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  272227. A s 180 pA a arc st
  272228. np X Y s Y 2 dv
  272229. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  272230. rO D rlineto
  272231. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  272232. rO lW -2 dv a Y lW 2 dv a rO a p l
  272233. lW -2 dv Y lW 2 dv a p l
  272234. 0 Y p l X Y p l X 0 p l cp f
  272235. 0 0 p M
  272236. 0 Y p l
  272237. X Y p l
  272238. X 0 p l cp
  272239. SM st}{Rr SM st}{rO Y p M rO rO xl
  272240. 0 Y X Y rO ac
  272241. X Y X 0 rO ac
  272242. X 0 0 0 rO ac
  272243. rO neg D xl X Y 0 Y rO ac
  272244. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  272245. -1 -1 sc LB whf}{Asc gs gLB gr
  272246. -0.4 -0
  272247. .4 sc LB whf}{Asc LB gs whf gr
  272248. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  272249. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  272250. gs 3.6 12 sc gOv gr
  272251. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  272252. gs 3.6 12 sc Cr whf gr
  272253. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  272254. 0 -1 p M
  272255. 0 0 1 0 1 ac
  272256. 8 0 8 1 1 ac
  272257. 8 0 16 0 1 ac
  272258. 16 0 16 -1 1 ac
  272259. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  272260. 2 dv D sc
  272261. 1 0 M -1 0 l
  272262. 0 1 M 0 -1 l
  272263. Ast}{XY D X Y dt 0 0 M SM cpt xl
  272264. 2 dv D sc
  272265. 1 0 M -1 0 l
  272266. Ast}{4.5 Aos
  272267. 1 0 M -1 0 l
  272268. 0 1 M 0 -1 l
  272269. 2 0 M 0 0 2 0 360 arc
  272270. Ast}{4.5 Aos
  272271. 1 0 M -1 0 l
  272272. 2 0 M 0 0 2 0 360 arc
  272273. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  272274. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  272275. 1 -1 M -1 -1 l
  272276. 0 2 M 0 -2 l
  272277. Ast}{5 Aos
  272278. 1 -1 M -1 -1 l
  272279. 1 1 M -1 1 l
  272280. 0 2 M 0 -2 l
  272281. Ast}{4.5 Aos
  272282. 1 0 M -1 0 l
  272283. 0 1 M 0 -1 l
  272284. Ast}{4.5 Aos
  272285. 1 0 M -1 0 l
  272286. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  272287. sc DLB gs whf gr
  272288. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  272289. gs 3.6 12 sc Cr whf gr
  272290. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  272291. gs 3.6 12 sc Cr blf gr
  272292. ZLB whf}{Asc LB gs whf gr
  272293. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  272294. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  272295. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  272296. e 2 ix a
  272297. }b/PT{D 2 4 gi al P OP D 1 sc
  272298. o length 6 gt{P 6 g}{e P 8 dv}ie
  272299. D lW 2 m lt{P lW 2 m}if
  272300. 0 e p
  272301. 0 0 p
  272302. 3 -1 r s 3 1 r e s e
  272303. 0 0 p M 1 0 p l
  272304. 0 0 p ap M 1 0 p ap l
  272305. e n e n
  272306. 0 0 p ap M 1 0 p ap l
  272307. P P}b
  272308. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  272309. cvi D 0 eq{P 1}if/nH x
  272310. D hS nH m s
  272311. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  272312. bW 2 dv/bd x
  272313. lW 2 dv e D NH e{D bd p M bd n p l}for
  272314. st gr}{gs 12 OB np
  272315. lW 2 dv 0 xl NH 1 sc
  272316. bW 2 dv wF
  272317.  m nH 1 a dv/bd x
  272318. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  272319. np 0 lW 2 dv o o n p M p l bW 2 dv
  272320. wF m o o p l n p l
  272321. cp f gr}{P}{gs 12 OB/bL x
  272322. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  272323. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  272324. bL nSq 2 m dv D sc
  272325. nSq{.135  .667 .865  .667 1 0 rcurveto
  272326. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  272327. np 0 lW 2 dv o o n p M p l bW 2 dv
  272328. wF m o o p l n p l
  272329. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  272330. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  272331. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  272332. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  272333. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  272334. 5 -1 r dv neg e 5 -1 r dv neg e
  272335. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  272336. %%EndProcSet
  272337. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  272338. 433 157 34 73 SPn/origstk x
  272339. 65535 65535 65535 sBg
  272340. 0 0 0 C
  272341. 997 3060 M
  272342. 979 3078 l
  272343. 859 2627 l
  272344. 881 2633 l
  272345. 1424 3176 
  272346. 1427 3187 l
  272347. 1399 3190 l
  272348. 979 3078 l
  272349. 997 3060 l
  272350. 1647 2954 M
  272351. 1661 2968 l
  272352. 1453 3175 l
  272353. 1427 3187 l
  272354. 1424 3176 l
  272355. 1623 2436 M
  272356. 1641 2418 l
  272357. 1723 2727 l
  272358. 1703 2733 l
  272359. 1196 2320 M
  272360. 1192 2298 l
  272361. 1641 2418 l
  272362. 1623 2436 l
  272363. 1192 2298 M
  272364. 1196 2320 l
  272365. 881 2633 l
  272366. 859 2627 l
  272367. f[1 3 1180 2257 1109 1993 ]Bd
  272368. 1571 3614 M
  272369. 1519 3638 l
  272370. 1399 3190 l
  272371. 1427 3187 l
  272372. 1453 3175 l
  272373. 1294 3891 M
  272374. 1280 3877 l
  272375. 1519 3638 l
  272376. 1571 3614 l
  272377. 2159 2617 M
  272378. 2125 2661 l
  272379. 1835 2828 l
  272380. 1825 2810 l
  272381. 2559 2848 M
  272382. 2535 2866 l
  272383. 2525 2892 l
  272384. 2125 2661 l
  272385. 2159 2617 l
  272386. 2545 3313 M
  272387. 2525 3327 l
  272388. 2525 2892 l
  272389. 2535 2866 l
  272390. 2545 2873 l
  272391. 2963 3449 M
  272392. 2971 3471 l
  272393. 2525 3327 l
  272394. 2545 3313 l
  272395. 3221 3092 M
  272396. 3233 3092 l
  272397. 3225 3120 l
  272398. 2971 3471 l
  272399. 2963 3449 l
  272400. 2963 2736 M
  272401. 2971 2714 l
  272402. 3225 3064 l
  272403. 3233 3092 l
  272404. 3221 3092 l
  272405. 2971 2714 M
  272406. 2963 2736 l
  272407. 2545 2873 l
  272408. 2535 2866 l
  272409. 2559 2848 l
  272410. f[1 3 2488 3347 2248 3486 ]Bd
  272411. [1 3 2981 2674 3051 2415 ]Bd
  272412. 3690 3064 M
  272413. 3684 3120 l
  272414. 3225 3120 l
  272415. 3233 3092 l
  272416. 3225 3064 l
  272417. 3786 3417 M
  272418. 3766 3423 l
  272419. 3684 3120 l
  272420. 3690 3064 l
  272421. 6250 3027 4570 3027 2 Ar
  272422. 7131 2717 M
  272423. 7125 2773 l
  272424. 6999 2303 l
  272425. 7021 2309 l
  272426. 7579 2837 M
  272427. 7567 2863 l
  272428. 7564 2891 l
  272429. 7125 2773 l
  272430. 7131 2717 l
  272431. 7790 2627 M
  272432. 7804 2641 l
  272433. 7578 2866 l
  272434. 7567 2863 l
  272435. 7579 2837 l
  272436. 7763 2112 M
  272437. 7781 2094 l
  272438. 7864 2407 l
  272439. 7844 2413 l
  272440. 7336 1996 M
  272441. 7332 1974 l
  272442. 7781 2094 l
  272443. 7763 2112 l
  272444. 7332 1974 M
  272445. 7336 1996 l
  272446. 7021 2309 l
  272447. 6999 2303 l
  272448. 7687 3275 M
  272449. 7681 33
  272450. 7564 2891 l
  272451. 7567 2863 l
  272452. 7578 2866 l
  272453. 8136 3396 M
  272454. 8124 3422 l
  272455. 8128 3452 l
  272456. 7681 3331 l
  272457. 7687 3275 l
  272458. 8421 3113 M
  272459. 8447 3101 l
  272460. 8449 3113 l
  272461. 8136 3424 l
  272462. 8124 3422 l
  272463. 8136 3396 l
  272464. 8303 2664 M
  272465. 8359 2658 l
  272466. 8477 3105 l
  272467. 8447 3101 l
  272468. 8421 3113 l
  272469. 8359 2658 M
  272470. 8303 2664 l
  272471. 7969 2574 l
  272472. 7975 2554 l
  272473. 8335 3817 M
  272474. 8323 3839 l
  272475. 8128 3452 l
  272476. 8124 3422 l
  272477. 8136 3424 l
  272478. 8769 3749 M
  272479. 8778 3758 l
  272480. 8752 3772 l
  272481. 8323 3839 l
  272482. 8335 3817 l
  272483. 8839 3315 M
  272484. 8861 3303 l
  272485. 8792 3732 l
  272486. 778 3758 l
  272487. 8769 3749 l
  272488. 8861 3303 M
  272489. 8839 3315 l
  272490. 8449 3113 l
  272491. 8447 3101 l
  272492. 8477 3105 l
  272493. f[1 3 7320 1930 7245 1654 ]Bd
  272494. [1 3 7648 3339 7426 3561 ]Bd
  272495. [1 3 8891 3286 9014 3214 ]Bd
  272496. 9121 4061 M
  272497. 9077 4097 l
  272498. 8752 3772 l
  272499. 8778 3758 l
  272500. 8792 3732 l
  272501. 8935 4383 M
  272502. 8917 4373 l
  272503. 9077 4097 l
  272504. 9121 4061 l
  272505. count origstk sub{P}rp end
  272506. chemsave restore
  272507.     Helvetica
  272508. Palatino
  272509. LiHMDS
  272510. C to rt
  272511. EtO2C5
  272512. LiHMDS
  272513. C to rt
  272514.     Helvetica
  272515. Palatinoa
  272516. Untitled preferences-1
  272517. count
  272518. currentpoint 192837465
  272519. currentpoint
  272520. save/chemsave exch def
  272521. %%BeginProcSet: chemdict30 24 10
  272522. % ChemDraw Laser Prep
  272523. % Copyright 198
  272524. 6-1993, Cambridge Scientific Computing, Inc.
  272525. userdict/chemdict30 210 dict put
  272526. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  272527. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  272528. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  272529. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  272530. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  272531. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  272532. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  272533. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  272534. x}b/s
  272535. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272536. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272537. 0 cw 2 dv xl
  272538. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  272539. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  272540. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  272541. St 16 and 0 ne{2 
  272542. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  272543. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  272544. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  272545. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  272546. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  272547. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  272548. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  272549. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  272550. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  272551. P P}{sq at 2
  272552. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  272553. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  272554. l w .
  272555. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  272556. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  272557. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  272558. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  272559.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  272560. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  272561. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  272562. 21 -10 27 -8 27 0 cv
  272563. 27 8 21 10 9 6 cv
  272564. -3 2 -3 -2 9 -6 cv
  272565. cp}b/DLB{0 0 M -4.8 4.8 l
  272566. -8 8 -9.6 12 -9.6 16.8 cv
  272567. -9.6 21
  272568. .6 -8 24.6 -4.8 25.8 cv
  272569. -1.6 27 1.6 27 4.8 25.8 cv
  272570. 8 24.6 9.6 21.6 9.6 16.8 cv
  272571. 9.6 12 8 8 4.8 4.8 cv
  272572. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  272573. 0 Y X Y rO ac
  272574. X Y X 0 rO ac
  272575. X 0 0 0 rO ac
  272576. 0 0 0 Y rO ac
  272577. cp}b/Rc{0 0 p M
  272578. 0 Y p l
  272579. X Y p l
  272580. X 0 p l
  272581. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  272582. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  272583. dtransform
  272584. m D 0 lt{n}if sq n D
  272585. CMT dtransform idtransform
  272586. e 2 m e
  272587. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  272588. 32 -0.5 0.5{gs
  272589. 13.5 0 xl
  272590. D 32 s 64 dv 13.5 m D 7 m 24 dv
  272591. -13.5 0 xl
  272592. gr}for
  272593. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  272594. 32 -0.5 0.5{gs
  272595. D 32 s 64 dv 0.65 m D
  272596. gr}for
  272597. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  272598. 32 -0.5 0.5{gs
  272599. D 32 s 64 dv D
  272600. gr}for
  272601. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  272602. 32 -0.5 0.5{gs
  272603. 0 13.5 xl
  272604. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  272605. 0 -13.5 xl
  272606. DLB f
  272607. gr}for
  272608. DLB SM s
  272609. t}{DLB grf}ie}b/gRr{sh{sRmp
  272610. 32 -0.5 0.5{gs
  272611. X 2 dv Y 2 dv xl
  272612. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  272613. X -2 dv Y -2 dv xl
  272614. gr}for
  272615. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  272616. 32 -0.5 0.5{gs
  272617. X 2 dv Y 2 dv xl
  272618. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  272619. X -2 dv Y -2 dv xl
  272620. gr}for
  272621. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  272622. rev{1 -1 sc}if
  272623. 0 lW 2 m xl
  272624. D SA OA
  272625. rad 0 xl
  272626. 180 ro
  272627. 0 lW 2 m xl
  272628. SA OA}b/Aos{X Y M SM 
  272629. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s e
  272630. o 0 lt o 0 lt ne/rev x
  272631. D 0 lt{1 -1 sc neg}if/Y x D 0 lt{-1 1 sc neg}if/X x np{{Y 16 div D 2 S lt{P 2 S}if/lp x
  272632. lp 0 p M 0 0 p l 0 Y p l lp Y p l
  272633. X lp s 0 p M X 0 p l X Y p l X lp s Y p l SM st}{Y 16 div D 2 S lt{P 2 S}if/lp x
  272634. lp 0 p M
  272635. 0 0 0 Y lp ac
  272636. 0 Y 2 dv lp neg o lp ac
  272637. 0 Y 2 dv 0 Y lp ac
  272638. 0 Y lp Y lp ac
  272639. X lp s 0 p M
  272640. X 0 X Y lp ac
  272641. X Y 2 dv X lp a o lp ac
  272642. X Y 2 dv X Y lp ac
  272643. X Y X lp s Y lp ac SM st}{Y D 2 dv Y 180 p
  272644. A s 180 pA a arc st
  272645. np X Y s Y 2 dv
  272646. Y pA D neg arcn st}{Rc SM st}{X lW 2 dv a lW -2 dv p M
  272647. rO D rlineto
  272648. X lW 2 dv a rO a Y lW 2 dv a rO a p l
  272649. rO lW -2 dv a Y lW 2 dv a rO a p l
  272650. lW -2 dv Y lW 2 dv a p l
  272651. 0 Y p l X Y p l X 0 p l cp f
  272652. 0 0 p M
  272653. 0 Y p l
  272654. X Y p l
  272655. X 0 p l cp
  272656. SM st}{Rr SM st}{rO Y p M rO rO xl
  272657. 0 Y X Y rO ac
  272658. X Y X 0 rO ac
  272659. X 0 0 0 rO ac
  272660. rO neg D xl X Y 0 Y rO ac
  272661. Rr st}{Ac st}{OrA gAc}{Ov st}{OrA 1 .4 sc gOv}{Asc LB whf}{Asc gLB}{Asc gs gLB gr
  272662. -1 -1 sc LB whf}{Asc gs gLB gr
  272663. -0.4 -0
  272664. .4 sc LB whf}{Asc LB gs whf gr
  272665. np -0.4 -0.4 sc gLB}{Asc DLB -1 -1 sc DLB gs whf gr
  272666. np 90 ro gs gDLB gr -1 -1 sc gDLB}{Asc gs -1 -1 sc ZLB whf gr
  272667. gs 3.6 12 sc gOv gr
  272668. ZLB whf}{Asc gs -1 -1 sc gZLB gr
  272669. gs 3.6 12 sc Cr whf gr
  272670. gZLB}{0 0 p M X Y p l SM st}{bW sl 0 0 p M X Y p l SM st}{dL 0 0 p M X Y p l SM st}{OrA 1 16 dv D sc
  272671. 0 -1 p M
  272672. 0 0 1 0 1 ac
  272673. 8 0 8 1 1 ac
  272674. 8 0 16 0 1 ac
  272675. 16 0 16 -1 1 ac
  272676. SM st}{XY D 0 0 dt X Y dt}{XY 2 dv X Y dt}{XY D X Y dt 0 0 M SM cpt xl
  272677. 2 dv D sc
  272678. 1 0 M -1 0 l
  272679. 0 1 M 0 -1 l
  272680. Ast}{XY D X Y dt 0 0 M SM cpt xl
  272681. 2 dv D sc
  272682. 1 0 M -1 0 l
  272683. Ast}{4.5 Aos
  272684. 1 0 M -1 0 l
  272685. 0 1 M 0 -1 l
  272686. 2 0 M 0 0 2 0 360 arc
  272687. Ast}{4.5 Aos
  272688. 1 0 M -1 0 l
  272689. 2 0 M 0 0 2 0 360 arc
  272690. Ast}{2.25 Ath}{1.5 Ath}{1 Ath}{2.25 Aeq}{1.5 Aeq}{1 Aeq}{OrA 1 16 dv D sc
  272691. 0 -1 p M 0 0 p l 16 0 p l 16 -1 p l SM st}{5 Aos
  272692. 1 -1 M -1 -1 l
  272693. 0 2 M 0 -2 l
  272694. Ast}{5 Aos
  272695. 1 -1 M -1 -1 l
  272696. 1 1 M -1 1 l
  272697. 0 2 M 0 -2 l
  272698. Ast}{4.5 Aos
  272699. 1 0 M -1 0 l
  272700. 0 1 M 0 -1 l
  272701. Ast}{4.5 Aos
  272702. 1 0 M -1 0 l
  272703. Ast}{gRc}{gRr}{Rc blf}{Rr blf}{Ac blf}{Ov blf}{Asc DLB -1 -1 
  272704. sc DLB gs whf gr
  272705. np 90 ro DLB -1 -1 sc DLB blf}{Asc gs -1 -1 sc ZLB blf gr
  272706. gs 3.6 12 sc Cr whf gr
  272707. ZLB blf}{Asc gs -1 -1 sc ZLB whf gr
  272708. gs 3.6 12 sc Cr blf gr
  272709. ZLB whf}{Asc LB gs whf gr
  272710. np -0.4 -0.4 sc LB blf}{Asc LB gs f gr gs SM st gr
  272711. np -0.4 -0.4 sc LB whf}{Asc LB blf}{Asc LB gs f gr gs SM st gr
  272712. np -1 -1 sc LB whf}{Ac whf}{OrA gAc}{Ac blf}{Ov whf}{OrA 1 .4 sc gOv}{Ov blf}}e 39 s g xc gr}ie}b/DS{np p M p l st}b/DD{gs dL DS gr}b/DB{gs 12 OB bW sl np 0 0 p M 0 p l st gr}b/ap{e 3 ix a
  272713. e 2 ix a
  272714. }b/PT{D 2 4 gi al P OP D 1 sc
  272715. o length 6 gt{P 6 g}{e P 8 dv}ie
  272716. D lW 2 m lt{P lW 2 m}if
  272717. 0 e p
  272718. 0 0 p
  272719. 3 -1 r s 3 1 r e s e
  272720. 0 0 p M 1 0 p l
  272721. 0 0 p ap M 1 0 p ap l
  272722. e n e n
  272723. 0 0 p ap M 1 0 p ap l
  272724. P P}b
  272725. f/DT{gs np PT SM st gr}b/NH{lW s D hS dv ru
  272726. cvi D 0 eq{P 1}if/nH x
  272727. D hS nH m s
  272728. D 0 lt{P .1 s nH dv}{nH 2 a dv D 0 xl 2 m s nH dv}ie}b/Bd{D type/arraytype ne{bs e g}if{{P}{{{DS}{DD}{gs 12 OB np
  272729. bW 2 dv/bd x
  272730. lW 2 dv e D NH e{D bd p M bd n p l}for
  272731. st gr}{gs 12 OB np
  272732. lW 2 dv 0 xl NH 1 sc
  272733. bW 2 dv wF
  272734.  m nH 1 a dv/bd x
  272735. 0 1 nH{D 1 a bd m o o p M n p l}for SM st gr}{P}{DB}{gs 12 OB
  272736. np 0 lW 2 dv o o n p M p l bW 2 dv
  272737. wF m o o p l n p l
  272738. cp f gr}{P}{gs 12 OB/bL x
  272739. bW 2 dv D lW lt{P lW}if/bd x np 0 0 p M
  272740. bL bd 4 m dv ru 2 o o lt{e}if P cvi/nSq x
  272741. bL nSq 2 m dv D sc
  272742. nSq{.135  .667 .865  .667 1 0 rcurveto
  272743. .135 -.667 .865 -.667 1 0 rcurveto}rp SM st gr}{gs 12 OB
  272744. np 0 lW 2 dv o o n p M p l bW 2 dv
  272745. wF m o o p l n p l
  272746. cp SM lW 0.8 m sl st gr}{P}{4 2 r gs OP/rad x 1 SA DA gr}{P}}o 1 g 1 s g e 2 4 gi a
  272747. 5 -1 r xc}{al P 8 ix 1 eq{DD}{DS}ie 5 -1 r 2 eq{DB}{DS}ie P}{DT}}o 0 g g xc}b
  272748. /SP{/sf x/lW x/bW x/cW x SPn}b/SPn{gs
  272749. count 9 ge 7 ix 192837465 eq and{7 -1 r P
  272750. 6 -2 r o o xl 7 -1 r s e 7 -1 r s e
  272751. 5 -1 r dv neg e 5 -1 r dv neg e
  272752. sc neg e neg e xl}{xl P P}ie 1 1 S dv D sc CMT currentmatrix P lW sl 4.0 setmiterlimit np}b
  272753. %%EndProcSet
  272754. 40 57 20 20 54 chemdict30 begin/hS x/sf x/lW x/bW x/cW x/sh T d
  272755. 583 109 12 81 SPn/origstk x
  272756. 65535 65535 65535 sBg
  272757. 0 0 0 C
  272758. 1133 1931 M
  272759. 1113 1943 l
  272760. 730 1722 l
  272761. 730 1698 l
  272762. 1074 1959 M
  272763. 1064 1977 l
  272764. 725 1781 l
  272765. 735 1763 l
  272766. 347 1943 M
  272767. 327 1931 l
  272768. 730 1698 l
  272769. 730 1722 l
  272770. 347 2280 M
  272771. 327 2280 l
  272772. 327 1931 l
  272773. 347 1943 l
  272774.  2385 M
  272775. 1113 2397 l
  272776. 1113 1943 l
  272777. 1133 1931 l
  272778. 1516 2606 M
  272779. 1516 2630 l
  272780. 1113 2397 l
  272781. 1133 2385 l
  272782. 1785 2451 M
  272783. 1795 2469 l
  272784. 1516 2630 l
  272785. 1516 2606 l
  272786. 2302 2606 M
  272787. 2302 2630 l
  272788. 2005 2458 l
  272789. 2015 2440 l
  272790. 2339 2970 M
  272791. 2319 2970 l
  272792. 2319 2603 l
  272793. 2339 2603 l
  272794. 2285 2970 M
  272795. 2265 2970 l
  272796. 2265 2603 l
  272797. 2285 2603 l
  272798. 2695 2379 M
  272799. 2695 2403 l
  272800. 2302 2630 l
  272801. 2302 2606 l
  272802. 2974 2540 M
  272803. 2964 2558 l
  272804. 2695 2403 l
  272805. 2695 2379 l
  272806. 2947 2587 M
  272807. 2937 2605 l
  272808. 2690 2462 l
  272809. 2700 2444 l
  272810. 6030 2430 3690 2430 2 Ar
  272811. 6540 2938 M
  272812. 6520 2950 l
  272813. 6520 2484 l
  272814. 6540 2496 l
  272815. 6797 3086 M
  272816. 6787 3104 l
  272817. 6520 2950 l
  272818. 6540 2938 l
  272819. 7307 2938 M
  272820. 7327 2950 l
  272821. 7015 3130 l
  272822. 7005 3112 l
  272823. 7307 2496 M
  272824. 7317 2490 l
  272825. 7327 2490 l
  272826. 7327 2950 l
  272827. 7307 2938 l
  272828. 6923 2274 M
  272829. 6923 2262 l
  272830. 6944 2262 l
  272831. 7307 2472 l
  272832. 7317 2490 l
  272833. 7307 2496 l
  272834. 6918 2253 M
  272835. 6923 2262 l
  272836. 6923 2274 l
  272837. 6540 2496 l
  272838. 6520 2484 l
  272839. 7608 3069 M
  272840. 7598 3087 l
  272841. 7312 2922 l
  272842. 7322 2904 l
  272843. 7580 3115 M
  272844. 7570 3133 
  272845. 7286 2968 l
  272846. 7296 2950 l
  272847. 7311 2026 M
  272848. 7316 2035 l
  272849. 7306 2053 l
  272850. 6944 2262 l
  272851. 6923 2262 l
  272852. 6918 2253 l
  272853. 7306 2053 M
  272854. 7316 2035 l
  272855. 7326 2065 l
  272856. 7327 2490 l
  272857. 7317 2490 l
  272858. 7307 2472 l
  272859. f[1 3 7367 2490 7670 2490 ]Bd
  272860. [1 3 6909 2209 6837 1941 ]Bd
  272861. 7513 1798 M
  272862. 7553 1838 l
  272863. 7326 2065 l
  272864. 7316 2035 l
  272865. 7296 2015 l
  272866. 10223 1980 M
  272867. 10209 1960 l
  272868. 10677 1960 l
  272869. 10663 1980 l
  272870. 10087 2398 M
  272871. 10076 2402 l
  272872. 10068 2394 l
  272873. 10209 1960 l
  272874. 10223 1980 l
  272875. 10358 2594 M
  272876. 10346 2610 l
  272877. 10076 2414 l
  272878. 076 2402 l
  272879. 10087 2398 l
  272880. 10800 2398 M
  272881. 10811 2402 l
  272882. 10796 2425 l
  272883. 10553 2602 l
  272884. 10541 2586 l
  272885. 10810 2370 M
  272886. 10811 2402 l
  272887. 10800 2398 l
  272888. 10663 1980 l
  272889. 10677 1960 l
  272890. 9775 2588 M
  272891. 9765 2570 l
  272892. 10068 2394 l
  272893. 10076 2402 l
  272894. 10076 2414 l
  272895. 9693 2960 M
  272896. 9673 2960 l
  272897. 9673 2730 l
  272898. 9693 2730 l
  272899. 10454 3000 M
  272900. 10434 3000 l
  272901. 10434 2790 l
  272902. 10454 2790 l
  272903. 10218 3101 M
  272904. 10216 3121 l
  272905. 9761 3097 l
  272906. 9763 3077 l
  272907. 10725 2948 M
  272908. 10735 2966 l
  272909. 10513 3094 l
  272910. 10503 3076 l
  272911. 10454 3470 
  272912. 10434 3470 l
  272913. 10434 3240 l
  272914. 10454 3240 l
  272915. 10212 3368 M
  272916. 10198 3354 l
  272917. 10334 3218 l
  272918. 10348 3232 l
  272919. 9395 3261 M
  272920. 9385 3243 l
  272921. 9480 3188 l
  272922. 9490 3206 l
  272923. 9945 2920 M
  272924. 9955 2938 l
  272925. 9753 3054 l
  272926. 9743 3036 l
  272927. 9693 3430 M
  272928. 9673 3430 l
  272929. 9673 3200 l
  272930. 9693 3200 l
  272931. 11106 2540 M
  272932. 11078 2588 l
  272933. 10796 2425 l
  272934. 10811 2402 l
  272935. 10810 2370 l
  272936. count origstk sub{P}rp end
  272937. chemsave restore
  272938.     Helvetica
  272939. Palatino
  272940.     (5S-MEPY)
  272941. DCM, reflux
  272942. 90% ee
  272943. COOMe
  272944.     catalyst:
  272945. ;    l'f
  272946. =    l*E
  272947. COOMe
  272948. Rh2(5S-MEPY)4
  272949. DCM, reflux
  272950. 90% ee
  272951.     caaRtalyst:W
  272952.     Helvetica
  272953. Palatinoa
  272954. Untitled preferences-2
  272955. count
  272956. currentpoint 192837465
  272957. currentpoint
  272958. save/chemsave exch def
  272959. %%BeginProcSet: chemdict30 24 10
  272960. % ChemDraw Laser Prep
  272961. % Copyright 198
  272962. 6-1993, Cambridge Scientific Computing, Inc.
  272963. userdict/chemdict30 210 dict put
  272964. chemdict30 begin/version 24 def/sv 10 def/b{bind def}bind def/L{load def}b/R{null def}b/d/def L/a/add L/al/aload L/as/astore L/at/atan L/cp/closepath L/cv/curveto L/cw/currentlinewidth L/cpt/currentpoint L/dv/div L/D/dup L/e/exch L/F/false L/f/fill
  272965. L/fa/forall L/g/get L/gi/getinterval L/gr/grestore L/gs/gsave L/ie/ifelse L/ix/index L/l/lineto L/mt/matrix L/M/moveto L/m/mul L/n/neg L/np/newpath L/pb/pathbbox L/P/p
  272966. op L/r/roll L/rm/rmoveto L/ro/rotate L/rp/repeat L/ru/round L/sc/scale
  272967. L/sl/setlinewidth L/sm/setmatrix L/st/stroke L/sp/strokepath L/sq/sqrt L/s/sub L/T/true L/tr/transform L/xl/translate L/xc/exec L/A R/N R/St R/X R/Y R/aL R/bL R/bS R/bd R/bs R/cX R/cY R/ch R/co R/fB R/fI R/fS R/fZ R/fl
  272968. R/ft R/iX R/iY R/idx R/lh R/llx R/lly R/lp R/nH R/nSq R/newdict R/ps R/rad R/rev R/sL R/sba R/sbl R/sbs R/sn R/spa R/tB R/typ R/urx R/ury R/w R/wF R/xX R/xY R/rBg R/gBg R/bBg R/gry R/rDst R/gDst R/bDst R/
  272969. sf 20 d/cW 20 d/lW 20 d/bW 75 d/wF
  272970. 1.5 d/aF 11.875 d/aR 0.263 d/aA 50 d/hS 54 d/pA 32 d/sh F d/S{sf m}b/dL{[hS] 0 setdash}b/o{1 ix}b/rot{3 -1 r}b/x{e d}b/CMT mt d/TM mt d/SM{CMT sm}b/XY{X D m Y D m a sq}b/s1 1 string d/fp{T charpath flattenpath}b/p{tr ru
  272971. 0.25 a e ru 0.25 a e itransform}b/C{65536. dv rot 65536. dv rot 65536. dv rot setrgbcolor}b/sg{D currenthsbcolor P rot sethsbcolor currenthsbcolor e P e P o s D m .001 gt{setgray}{P}ie}b/sBg{65535 dv/bBg x 65535 dv/gBg x 65535 dv/rBg
  272972. x}b/s
  272973. Rmp{currentrgbcolor bBg e s/bDst x gBg e s/gDst x rBg e s/rDst x}b/N 0 d/db{array/bs x/N 0 d}b/B{bs N rot put/N N 1 a d}b/SpA{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272974. aR aL m n D aL a 0 p M 0 o n aA n aA arc cp f gr}b/SpH{gs np o o xl rot s e rot s o 0 ne o 0 ne or{at ro}{P P}ie
  272975. 0 cw 2 dv xl
  272976. aR aL m n D aL a 0 p M 0 o n aA n 0 arc cp f gr}b/Sp{/St x 0.316/aR x gs
  272977. aF lW m 0.8 m St 4 and 0 ne{bW m lW dv bW sl}if/aL x
  272978. St 8 and 0 ne{8 ix 8 ix 3 ix 3 ix SpA}if
  272979. St 16 and 0 ne{2 
  272980. ix 6 m 1 a D ix e D ix e D ix e D ix e P SpA}if
  272981. St 32 and 0 ne{8 ix 8 ix 3 ix 3 ix SpH}if
  272982. St 64 and 0 ne{2 ix 6 m 1 a D ix e D ix e D ix e D ix e P SpH}if
  272983. St 2 and 0 ne{St 4 and 0 ne{[hS bW m lW dv] 0 setdash}{dL}ie}if
  272984. np M{cv}rp St 128 and 0 ne{f}{st}ie gr}b/Ha{gs np 3 1 r
  272985. xl D sc -.7 1.4 p M 0.7 1.4 p l -.7 2.4 p M 0.7 2.4 p l SM st gr}b/OP{3 ix 3 ix xl 3 -1 r s 3 1 r
  272986. e s o o at ro D m e D m a sq}b/OB{/bS x OP D bS dv D lW 2 m lt{P lW 2 m}if/bd x}b/DA{np 0 0 M aL 0 aR aL m 180 aA s 180 a
  272987. A a arc cp f}b/OA{np 0 cw -2 dv M aL 0 aR aL m 180 aA s
  272988. 180 arc 0 cw -2 dv rlineto cp f}b/Ast{SM cw 0.8 m sl st}b/SA{aF m lW m/aL x 0.263/aR x aL 1 aR s m np 0 p M rad 0 p l gs Ast gr}b/CA{aF lW m 0.8 m/aL x 0.316/aR x aL 1 aR s m 2 dv rad D m o D m s D 0 le{P
  272989. P P}{sq at 2
  272990. m np rad 0 rad 180 6 -1 r s 180 6 -1 r s arc gs Ast gr cpt
  272991. e at ro}ie}b/AA{np rad 0 rad 180 180 6 -1 r a arc gs SM st gr}b/RA{lW m/w x np rad w p M w .7 dv w p l rad w n p M w .7 dv w n p l w .35 dv w 2 m p M 0 0 p
  272992. l w .
  272993. 35 dv w -2 m p l st}b/HA{lW m/w x np 0 0 p M w 2 m D p l w 2 m w p l rad w p l rad w n p l w 2 m
  272994. w n p l w 2 m D n p l cp st}b/Ar1{gs 5 1 r OP/rad x{{2.25 SA DA}{1.5 SA DA}{1 SA DA}{lW 4 m sl 4.5 SA DA}{lW 4 m sl 3 SA DA}{lW 4 m sl 2 SA
  272995. DA}{270 CA DA}{180 CA DA}{120 CA DA}{90 CA DA}{2.5 RA}{2.5 HA}{1 -1 sc 270 CA DA}{1 -1 sc 180 CA DA}{1 -1 sc 120 CA DA}{1 -1 sc 90 CA
  272996. DA}{5 RA}{5 HA}{dL 2.25 SA DA}{dL 1.5 SA DA}{dL 1 SA DA}{2.25 SA OA}{1.5 SA OA}{1 SA OA}{1 -1 sc 2.25 SA OA}{1 -1 sc 1.5 SA
  272997.  OA}{1 -1 sc 1 SA OA}{270 CA OA}{180 CA OA}{120 CA OA}{90 CA OA}{1 -1 sc 270 CA
  272998. OA}{1 -1 sc 180 CA OA}{1 -1 sc 120 CA OA}{1 -1 sc 90 CA OA}{1 -1 sc 270 AA}{1 -1 sc 180 AA}{1 -1 sc 120 AA}{1 -1 sc 90 AA}}e g xc
  272999. gr}b/ac{arcto 4{P}rp}b/rO{4 lW m}b/Cr{0 0 1 0 360 arc}b/Ac{XY D sc Cr SM}b/OrA{Y X at ro XY D rev{neg}if sc}b/Ov{OrA 1 0.4 sc Cr SM}b/Asc{OrA 1 27 dv D sc}b/LB{9 -6 M
  273000. 21 -10 27 -8 27 0 cv
  273001. 27 8 21 10 9 6 cv
  273002. -3 2 -3 -2 9 -6 cv
  273003. cp}b/DLB{0 0 M -4.8 4.8 l
  273004. -8 8 -9.6 12 -9.6 16.8 cv
  273005. -9.6 21
  273006. .6 -8 24.6 -4.8 25.8 cv
  273007. -1.6 27 1.6 27 4.8 25.8 cv
  273008. 8 24.6 9.6 21.6 9.6 16.8 cv
  273009. 9.6 12 8 8 4.8 4.8 cv
  273010. cp}b/ZLB{LB}b/dt{gs np M SM cpt np rot 4.5 dv 0 360 arc f gr}b/whf{gs 1 setgray f gr SM st}b/blf{gs f gr SM st}b/Rr{0 rO p M
  273011. 0 Y X Y rO ac
  273012. X Y X 0 rO ac
  273013. X 0 0 0 rO ac
  273014. 0 0 0 Y rO ac
  273015. cp}b/Rc{0 0 p M
  273016. 0 Y p l
  273017. X Y p l
  273018. X 0 p l
  273019. cp}b/grf{gs 0.5 sg f gr SM st}b/gG{D 32 dv D m 1 e s/gry x
  273020. currentrgbcolor bDst gry m a 3 1 r gDst gry m a 3 1 r rDst gry m a 3 1 r setrgbcolor}b/gS{dtransform CMT i
  273021. dtransform
  273022. m D 0 lt{n}if sq n D
  273023. CMT dtransform idtransform
  273024. e 2 m e
  273025. 7 m 32 a 256 dv D sc}b/gLB{sh{sRmp
  273026. 32 -0.5 0.5{gs
  273027. 13.5 0 xl
  273028. D 32 s 64 dv 13.5 m D 7 m 24 dv
  273029. -13.5 0 xl
  273030. gr}for
  273031. LB SM st}{LB grf}ie}b/gOv{sh{sRmp
  273032. 32 -0.5 0.5{gs
  273033. D 32 s 64 dv 0.65 m D
  273034. gr}for
  273035. Cr SM st}{Cr grf}ie}b/gAc{sh{sRmp
  273036. 32 -0.5 0.5{gs
  273037. D 32 s 64 dv D
  273038. gr}for
  273039. Cr SM st}{Cr grf}ie}b/gDLB{sh{sRmp
  273040. 32 -0.5 0.5{gs
  273041. 0 13.5 xl
  273042. D 32 s 64 dv 13.5 m D 7 m 24 dv e
  273043. 0 -13.5 xl
  273044. DLB f
  273045. gr}for
  273046. DLB SM s
  273047. t}{DLB grf}ie}b/gRr{sh{sRmp
  273048. 32 -0.5 0.5{gs
  273049. X 2 dv Y 2 dv xl
  273050. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  273051. X -2 dv Y -2 dv xl
  273052. gr}for
  273053. Rr SM st}{Rr grf}ie}b/gRc{sh{sRmp
  273054. 32 -0.5 0.5{gs
  273055. X 2 dv Y 2 dv xl
  273056. D 32 s 64 dv X Y lt{X}{Y}ie m 0.25 m D
  273057. X -2 dv Y -2 dv xl
  273058. gr}for
  273059. Rc SM st}{Rc grf}ie}b/gZLB{gLB}b/Ath{Y X at ro XY 2 dv/rad x gs D SA DA gr rad 2 m 0 xl 180 ro SA DA}b/Aeq{Y X at ro XY/rad x
  273060. rev{1 -1 sc}if
  273061. 0 lW 2 m xl
  273062. D SA OA
  273063. rad 0 xl
  273064. 180 ro
  273065. 0 lW 2 m xl
  273066. SA OA}b/Aos{X Y M SM 
  273067. cpt xl XY e dv D sc}b/Ar{D 39 lt{Ar1}{gs 5 1 r o o xl 3 -1 r e s 3 1 r s