Name reactions: a collection of detailed reaction mechanisms ; [more than 300 reactions]
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Berlin [u.a.]
Springer
2002
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| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | XVIII, 416 S. graph. Darst. |
| ISBN: | 3540430245 |
Internformat
MARC
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| 084 | |a CHE 620b |2 stub | ||
| 100 | 1 | |a Li, Jie Jack |d 1964- |e Verfasser |0 (DE-588)123481848 |4 aut | |
| 245 | 1 | 0 | |a Name reactions |b a collection of detailed reaction mechanisms ; [more than 300 reactions] |c Jie Jack Li |
| 264 | 1 | |a Berlin [u.a.] |b Springer |c 2002 | |
| 300 | |a XVIII, 416 S. |b graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 650 | 4 | |a Chimie organique | |
| 650 | 4 | |a Réactions organiques (Chimie) | |
| 650 | 4 | |a Chemical reactions | |
| 650 | 4 | |a Chemistry, Organic | |
| 650 | 0 | 7 | |a Reaktionsmechanismus |0 (DE-588)4177123-0 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Namensreaktion |0 (DE-588)4171139-7 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Organische Chemie |0 (DE-588)4043793-0 |2 gnd |9 rswk-swf |
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| 883 | 1 | |8 2\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
| 943 | 1 | |a oai:aleph.bib-bvb.de:BVB01-009668946 | |
Datensatz im Suchindex
| _version_ | 1823033875229573120 |
|---|---|
| adam_text |
TABLE OF CONTENTS
PREFACE
.XIII
ABBREVIATIONS.XV
1. ABNORMAL CLAISEN
REARRANGEMENT.1
2. ALDER ENE
REACTION.2
3. ALLAN-ROBINSON
REACTION.3
4. ALPER
CARBONYLATION.5
5. AMADORI GLUCOSAMINE
REARRANGEMENT.7
6. ANGELI-RIMINI HYDROXAMIC ACID
SYNTHESIS.8
7. ANRORC MECHANISM
.9
8. ARNDT-EISTERT HOMOLOGATION
.10
9. BAEYER-DREWSON INDIGO
SYNTHESIS.11
10. BAEYER-VILLIGER OXIDATION
.13
11. BAKER-VENKATARAMAN REARRANGEMENT
.14
12. BAMBERGER REARRANGEMENT
.15
13. BAMFORD-STEVENS
REACTION.16
14. BARGELLINI REACTION
.17
15. BARTOLI INDOLE SYNTHESIS
.18
16. BARTON DECARBOXYLATION
.20
17. BARTON-MCCOMBIE
DEOXYGENATION.21
18. BARTON NITRITE PHOTOLYSIS
.22
19. BAYLIS-HILLMAN
REACTION.23
20. BECKMANN
REARRANGEMENT.25
21. BEIRUT REACTION
.26
22. BENZILIC ACID REARRANGEMENT
.28
23. BENZOIN
CONDENSATION.29
24. BERGMAN
CYCLIZATION.30
25. BIGINELLI PYRIMIDONE SYNTHESIS
.31
26. BIRCH
REDUCTION.33
27. BISCHLER-MOEHLAU INDOLE
SYNTHESIS.35
28. BISCHLER-NAPIERALSKI
REACTION.36
29. BLAISE REACTION
.37
30. BLANC CHLOROMETHYLATION
REACTION.38
31. BOEKELHEIDE REACTION
.39
32. BOGER PYRIDINE SYNTHESIS
.40
33. BOORD
REACTION.41
34. BORSCHE-DRECHSEL CYCLIZATION
.42
35. BOULTON-KATRITZKY REARRANGEMENT
.43
36. BOUVEAULT ALDEHYDE
SYNTHESIS.44
37. BOUVEAULT-BLANC REDUCTION
.45
38. BOYLAND-SIMS
OXIDATION.46
39. BRADSHER
REACTION.48
40. BROOK
REARRANGEMENT.49
41. BROWN HYDROBORATION
REACTION.50
42. BUCHERER CARBAZOLE SYNTHESIS
.51
43. BUCHERER REACTION
.52
44. BUCHERER-BERGS REACTION
.53
45. BUCHNER-CURTIUS-SCHLOTTERBECK
REACTION.54
46. BUCHNER METHOD OF RING
EXPANSION.55
47. BUCHWALD-HARTWIG C-N BOND AND C-O BOND FORMATION REACTIONS
.56
48. BURGESS DEHYDRATING REAGENT
.57
49. CADIOT-CHODKIEWICZ COUPLING
.58
50. CANNIZZARO DISPROPOTIONATION
REACTION.59
51. CARROLL
REARRANGEMENT.60
52. CASTRO-STEPHENS COUPLING
.61
53. CHAPMAN
REARRANGEMENT.62
54. CHICHIBABIN AMINATION
REACTION.63
55. CHICHIBABIN PYRIDINE
SYNTHESIS.64
56. CHUGAEV
REACTION.66
57. CIAMICIAN-DENNSTED
REARRANGEMENT.67
58. CLAISEN, ESCHENMOSER-CLAISEN, JOHNSON-CLAISENAND, AND IRELAND-
CLAISEN REARRANGEMENTS
.68
59. CLARK-ESCHWEILER REDUCTIVE ALKYLATION OF AMINES
.70
60. COMBES QUINOLINE SYNTHESIS
.71
61. CONRAD-LIPACH REACTION
.73
62. COPE ELIMINATION
REACTION.74
63. COPE, OXY-COPE, AND ANIONIC OXY-COPE REARRANGEMENTS
.75
64. COREY
YY
CHAYKOVSKY EPOXIDATION
.77
65. COREY-FUCHS
REACTION.78
66. COREY-BAKSHI-SHIBATA (CBS)
REDUCTION.79
67. COREY-KIM
OXIDATION.81
68. COREY-WINTER OLEFIN SYNTHESIS
.82
69. CORNFORTH REARRANGEMENT
.84
70. CRIEGEE GLYCOL
CLEAVAGE.85
71. CRIEGEE MECHANISM OF
OZONOLYSIS.86
72. CURTIUS REARRANGEMENT
.87
73. DAKIN REACTION
.88
74. DAKIN-WEST REACTION
.89
75. DANHEISER
ANNULATION.90
76. DARZENS GLYCIDIC ESTER
CONDENSATION.91
77. DAVIS CHIRAL OXAZIRIDINE
REAGENT.92
78. DE MAYO
REACTION.93
79. DEMJANOV REARRANGEMENT
.95
80. DESS-MARTIN PERIODINANE
OXIDATION.96
81. DIECKMANN
CONDENSATION.97
82. DIELS-ALDER REACTION, REVERSE ELECTRONIC DEMAND DIELS-ALDER
REACTION,
HETERO-DIELS-ALDER REACTION
.98
83. DIENONE-PHENOL
REARRANGEMENT.100
84. DI
YY
-METHANE
REARRANGEMENT.101
85. DOEBNER REACTION
.102
86. DOEBNER-VON MILLER
REACTION.104
87. DOERING-LAFLAMME ALLENE
SYNTHESIS.106
88. DORNOW-WIEHLER ISOXAZOLE
SYNTHESIS.107
89. DOETZ REACTION
.109
90. DUTT-WORMALL
REACTION.110
91. ESCHENMOSER COUPLING
REACTION.111
92. ESCHENMOSER-TANABE
FRAGMENTATION.112
93. ETARD REACTION
.113
94. EVANS ALDOL REACTION
.114
95. FAVORSKII REARRANGEMENT AND QUASI-FAVORSKII
REARRANGEMENT.116
96. FEIST-BENARY FURAN
SYNTHESIS.118
97. FERRIER REARRANGEMENT
.119
98. FISCHER-HEPP
REARRANGEMENT.120
99. FISCHER INDOLE
SYNTHESIS.121
100. FISCHER-SPEIER ESTERIFICATION
.122
101. FLEMING
OXIDATION.123
102. FORSTER
REACTION.125
103. FRATER-SEEBACH ALKYLATION
.127
104. FRIEDEL-CRAFTS REACTION
.128
105. FRIEDLAENDER
SYNTHESIS.130
106. FRIES
REARRANGEMENT.132
107. FRITSCH-BUTTENBERG-WIECHELL
REARRANGEMENT.133
108. FUJIMOTO-BELLEAU REACTION
.134
109. FUKUYAMA AMINE
SYNTHESIS.135
110. GABRIEL SYNTHESIS
.137
111. GASSMAN INDOLE
SYNTHESIS.138
112. GATTERMANN-KOCH
REACTION.139
113. GEWALD AMINOTHIOPHENE SYNTHESIS
.140
114. GLASER
COUPLING.142
115. GOMBERG-BACHMANN REACTION
.143
116. GRIBBLE INDOLE
REDUCTION.144
117. GRIBBLE REDUCTION OF DIARYL
KETONES.145
118. GROB FRAGMENTATION
.146
119. GUARESCHI-THORPE CONDENSATION
.148
120. HAJOS-WIECHERT REACTION
.149
121. HALLER-BAUER
REACTION.151
122. HANTZSCH PYRIDINE SYNTHESIS
.152
123. HANTZSCH PYRROLE
SYNTHESIS.154
124. HAWORTH REACTION
.155
125. HAYASHI
REARRANGEMENT.156
126. HECK
REACTION.158
127. HEGEDUS INDOLE
SYNTHESIS.160
128. HELL-VOLHARDT-ZELINSKY REACTION
.161
129. HENRY REACTION (NITROALDOL REACTION)
.162
130. HERZ REACTION
.163
131. HETEROARYL HECK
REACTION.164
132. HIYAMA CROSS-COUPLING
REACTION.165
133. HODGES-VEDEJS METALLATION OF
OXAZOLES.167
134. HOFMANN REARRANGEMENT (HOFMANN DEGRADATION
REACTION).168
135. HOFMANN-LOEFFLER-FREYTAG
REACTION.169
136. HOFMANN-MARTIUS REACTION (REILLY-HICKINBOTTOM REARRANGEMENT)
.170
137. HOOKER
OXIDATION.172
138. HORNER-WADSWORTH-EMMONS REACTION
.174
139. HOUBEN-HOESCH
SYNTHESIS.176
140. HUNSDIECKER
REACTION.178
141. ING-MANSKE
PROCEDURE.179
142. JACOBSEN-KATSUKI EPOXIDATION
.180
143. JACOBSEN
REARRANGEMENT.182
144. JAPP-KLINGEMANN HYDRAZONE
SYNTHESIS.184
145. JULIA-LYTHGOE
OLEFINATION.185
146. KAHNE
GLYCOSIDATION.186
147. KECK STEREOSELECTIVE
ALLYLATION.188
148. KECK
MACROLACTONIZATION.190
149. KEMP
ELIMINATION.192
150. KENNEDY OXIDATIVE CYCLIZATION
.193
151. KHARASCH ADDITION
REACTION.194
152. KNOEVENAGEL
CONDENSATION.195
153. KNORR PYRROLE SYNTHESIS
.197
154. KOCH CARBONYLATION REACTION (KOCH-HAAF CARBONYLATION
REACTION).198
155. KOENIGS-KNORR
GLYCOSIDATION.200
156. KOLBE-SCHMITT
REACTION.201
157. KOSTANECKI REACTION
.202
158. KRAPCHO
DECARBOXYLATION.204
159. KROEHNKE REACTION (PYRIDINE
SYNTHESIS).205
160. KUMADA CROSS-COUPLING REACTION
.207
161. LAROCK INDOLE
SYNTHESIS.209
162. LAWESSON'S REAGENT
.210
163. LEUCKART-WALLACH
REACTION.211
164. LIEBEN HALOFORM REACTION
.212
165. LIEBESKIND-SROGL
COUPLING.213
166. LOSSEN
REARRANGEMENT.214
167. LUCHE
REDUCTION.215
168. MCFADYEN-STEVENS REDUCTION
.216
169. MCLAFFERTY
REARRANGEMENT.217
170. MCMURRY COUPLING
.218
171. MADELUNG INDOLE SYNTHESIS
.219
172. MANNICH
REACTION.220
173. MARSHALL BORONATE
FRAGMENTATION.221
174. MARTIN'S SULFURANE DEHYDRATING
REAGENT.222
175. MASAMUNE-ROUSH
CONDITIONS.223
176. MEERWEIN
ARYLATION.225
177. MEERWEIN-PONNDORF-VERLEY REDUCTION
.226
178. MEINWALD
REARRANGEMENT.227
179. MEISENHEIMER COMPLEX
.228
180. MEISENHEIMER REARRANGEMENT
.230
181. MEYER-SCHUSTER
REARRANGEMENT.231
182. MICHAEL
ADDITION.232
183. MICHAELIS-ARBUZOV PHOSPHONATE
SYNTHESIS.233
184. MIDLAND REDUCTION
.234
185. MILLER-SNYDER ARYL CYANIDE
SYNTHESIS.235
186. MISLOW-EVANS REARRANGEMENT
.237
187. MITSUNOBU
REACTION.238
188. MIYAURA BORATION REACTION
.239
189. MOFFATT
OXIDATION.240
190. MORGAN-WALLS REACTION (PICTET-HUBERT
REACTION).241
191. MORI-BAN INDOLE
SYNTHESIS.242
192. MORIN
REARRANGEMENT.244
193. MUKAIYAMA ALDOL REACTION
.246
194. MUKAIYAMA ESTERIFICATION
.247
195. MYERS
YY
SAITO
CYCLIZATION.249
196. NAMETKIN REARRANGEMENT (RETROPINACOL
REARRANGEMENT).250
197. NAZAROV
CYCLIZATION.251
198. NEBER REARRANGEMENT
.252
199. NEF REACTION
.253
200. NEGISHI CROSS-COUPLING REACTION
.254
201. NENITZESCU INDOLE
SYNTHESIS.255
202. NICHOLAS
REACTION.257
203. NOYORI ASYMMETRIC HYDROGENATION
.258
204. NOZAKI-HIYAMA-KISHI REACTION
.260
205. OPPENAUER OXIDATION
.261
206. ORTON
REARRANGEMENT.262
207. OVERMAN REARRANGEMENT
.264
208. PAAL-KNORR FURAN
SYNTHESIS.265
209. PAAL-KNORR PYRROLE
SYNTHESIS.266
210. PARHAM CYCLIZATION
.267
211. PASSERINI
REACTION.269
212. PATERNO-BUECHI REACTION
.270
213. PAUSON-KHAND CYCLOPENTENONE SYNTHESIS
.271
214. PAYNE REARRANGEMENT
.273
215. PECHMANN CONDENSATION (COUMARIN SYNTHESIS)
.274
216. PECHMANN PYRAZOLE SYNTHESIS
.275
217. PERKIN REACTION (CINNAMIC ACID SYNTHESIS)
.276
218. PERKOW VINYL PHOSPHATE
SYNTHESIS.278
219. PETERSON
OLEFINATION.279
220. PFAU-PLATTNER AZULENE
SYNTHESIS.280
221. PFITZINGER QUINOLINE
SYNTHESIS.281
222. PICTET-GAMS ISOQUINOLINE SYNTHESIS
.282
223. PICTET-SPENGLER ISOQUINOLINE SYNTHESIS
.283
224. PINACOL
REARRANGEMENT.284
225. PINNER
SYNTHESIS.285
226. POLONOVSKI REACTION
.286
227. POLONOVSKI-POTIER
REARRANGEMENT.288
228. POMERANZ-FRITSCH
REACTION.289
229. PREVOST
TRANS-DIHYDROXYLATION.291
230. PRILEZHAEV REACTION
.292
231. PRINS
REACTION.293
232. PSCHORR RING
CLOSURE.294
233. PUMMERER REARRANGEMENT
.296
234. RAMBERG-BAECKLUND OLEFIN SYNTHESIS
.297
235. REFORMATSKY REACTION
.298
236. REGITZ DIAZO SYNTHESIS
.299
237. REIMER-TIEMANN REACTION
.301
238. REISSERT REACTION (ALDEHYDE
SYNTHESIS).303
239. RILEY OXIDATION (SELENIUM DIOXIDE OXIDATION)
.305
240. RING-CLOSING METATHESIS (RCM) USING GRUBBS AND SCHROCK CATALYSTS
.306
241. RITTER
REACTION.308
242. ROBINSON
ANNULATION.309
243. ROBINSON-SCHOEPF
REACTION.310
244. ROUSH ALLYLBORONATE
REAGENT.312
245. RUBOTTOM
OXIDATION.313
246. RUPE REARRANGEMENT
.314
247. RYCHNOVSKY POLYOL SYNTHESIS
.315
248. SAKURAI ALLYLATION REACTION (HOSOMI-SAKURAI
REACTION).317
249. SANDMEYER REACTION
.319
250. SARETT OXIDATION
.320
251. SCHIEMANN REACTION (BALZ
YY
SCHIEMANN REACTION).321
252. SCHLOSSER MODIFICATION OF THE WITTIG REACTION
.322
253. SCHMIDT
REACTION.323
254. SCHMIDT'S TRICHLOROACETIMIDATE GLYCOSIDATION
REACTION.324
255. SCHOLL
REACTION.326
256. SCHOEPF
REACTION.328
257. SCHOTTEN-BAUMANN
REACTION.329
258. SHAPIRO
REACTION.330
259. SHARPLESS ASYMMETRIC
AMINOHYDROXYLATION.331
260. SHARPLESS ASYMMETRIC EPOXIDATION
.333
261. SHARPLESS DIHYDROXYLATION
.335
262. SHI ASYMMETRIC EPOXIDATION
.338
263. SIMMONS-SMITH REACTION
.340
264. SIMONINI REACTION
.341
265. SIMONIS CHROMONE CYCLIZATION
.342
266. SKRAUP QUINOLINE
SYNTHESIS.344
267. SMILES REARRANGEMENT
.346
268. SOMMELET
REACTION.347
269. SOMMELET-HAUSER (AMMONIUM YLIDE)
REARRANGEMENT.349
270. SONOGASHIRA REACTION
.350
271. STAUDINGER
REACTION.352
272. STETTER REACTION (MICHAEL
YY
STETTER REACTION).353
273. STEVENS
REARRANGEMENT.355
274. STIEGLITZ
REARRANGEMENT.357
275. STILL-GENNARI PHOSPHONATE
REACTION.358
276. STILLE
COUPLING.359
277. STILLE-KELLY
REACTION.360
278. STOBBE
CONDENSATION.362
279. STOLLE
SYNTHESIS.363
280. STORK ENAMINE
REACTION.364
281. STRECKER AMINO ACID
SYNTHESIS.365
282. SUZUKI
COUPLING.367
283. SWERN
OXIDATION.358
284. TAMAO-KUMADA OXIDATION
.370
285. TEBBE OLEFINATION (PETASIS ALKENYLATION)
.371
286. THORPE-ZIEGLER REACTION
.372
287. TIEMANN
REARRANGEMENT.373
288. TIFFENEAU-DEMJANOV
REARRANGEMENT.374
289. TISHCHENKO
REACTION.375
290. TOLLENS REACTION
.376
291. TSUJI-TROST ALLYLATION
.377
292. UENO-STORK CYCLIZATION
.378
293. UGI REACTION
.379
294. ULLMANN REACTION
.380
295. VILSMEIER-HAACK REACTION
.381
296. VON BRAUN REACTION
.383
297. VON RICHTER REACTION
.384
298. WACKER
OXIDATION.385
299. WAGNER-MEERWEIN REARRANGEMENT
.386
300. WALLACH
REARRANGEMENT.387
301. WEINREB
AMIDE.388
302. WEISS REACTION
.389
303. WHARTON OXYGEN TRANSPOSITION
REACTION.391
304. WILLGERODT-KINDLER
REACTION.392
305. WITTIG
REACTION.396
306. [1,2]-WITTIG
REARRANGEMENT.397
307. [2,3]-WITTIG
REARRANGEMENT.398
308. WOHL-ZIEGLER
REACTION.399
309. WOLFF REARRANGEMENT
.400
310. WOLFF-KISHNER
REDUCTION.401
311. WOODWARD
CIS-DIHYDROXYLATION
.402
312. YAMADA COUPLING
REAGENT.403
313. YAMAGUCHI
ESTERIFICATION.404
314. ZAITSEV
ELIMINATION.406
315. ZININ BENZIDINE REARRANGEMENT (SEMIDINE
REARRANGEMENT).407
SUBJECT
INDEX.409
PREFACE
WHAT'S IN A NAME? THAT WHICH WE CALL A ROSE BY ANY OTHER NAME WOULD
SMELL AS
SWEET.
A
ON THE OTHER HAND, NAME REACTIONS IN ORGANIC CHEMISTRY AND THE CORRE
SPONDING MECHANISMS ARE NEVERTHELESS FASCINATING FOR THEIR FAR-REACHING
UTILITY AS
WELL AS THEIR INSIGHT INTO ORGANIC REACTIONS. FURTHERMORE, UNDERSTANDING
THEIR
MECHANISMS GREATLY ENHANCES OUR ABILITY TO SOLVE MORE COMPLEX CHEMICAL
PROB
LEMS. AS A MATTER OF FACT, SOME NAME REACTIONS ARE THE DIRECT RESULT OF
BETTER UN
DERSTANDING OF THE MECHANISMS, AS EXEMPLIFIED BY THE BARTON-MCCOMBIE
REAC
TION.
B
IN ADDITION, OUR KNOWLEDGE OF HOW REACTIONS WORK CAN SHED LIGHT ON SIDE
REACTIONS AND BY-PRODUCTS, OR WHEN A REACTION DOES NOT GIVE THE
"DESIRED" PRODUCT,
THE MECHANISM MAY PROVIDE CLUES TO WHERE THE REACTION HAS GONE AWRY.
I STARTED COLLECTING NAMED AND UNNAMED ORGANIC REACTIONS AND THEIR MECHA
NISMS WHILE I WAS A GRADUATE STUDENT. IT OCCURRED TO ME THAT MANY OF MY
FELLOW
PRACTITIONERS ARE DOING EXACTLY THE SAME, AND THAT THESE EFFORTS COULD
BE MADE EAS
IER THROUGH A MONOGRAPH TABULATING INTERESTING AND USEFUL MECHANISMS OF
NAME
REACTIONS. TO THIS END, I HAVE UPDATED MY COLLECTION WITH MANY
CONTEMPORARY
NAME REACTIONS AND ADDED MORE RECENT REFERENCES, ESPECIALLY UP-TO-DATE
REVIEW AR
TICLES. IN REFLECTING THE ADVENT OF ASYMMETRIC SYNTHESIS, RELEVANT NAME
REACTIONS IN
THIS FIELD HAVE BEEN INCLUDED TO THE REPERTOIRE. SINCE THE STEP-BY-STEP
MECHANISMS
DELINEATED WITHIN ARE MOSTLY SELF-EXPLANATORY, DETAILED VERBAL
EXPLANATIONS ARE NOT
OFFERED, ALTHOUGH SOME IMPORTANT JARGONS ENTAILING THE TYPES OF
TRANSFORMATIONS
ARE HIGHLIGHTED. FOR SOME REACTIONS, SHORT DESCRIPTIONS ARE GIVEN AS
MNEMONICS
RATHER THAN ACCURATE DEFINITIONS. WITH REGARD TO THE REFERENCES, THE
FIRST ONE IS GEN
ERALLY THE ORIGINAL ARTICLE, WHEREAS THE REST ARE ARTICLES AND REVIEW
ARTICLES. READERS
INTERESTED IN IN-DEPTH COVERAGE OF NAME REACTIONS ARE ENCOURAGED TO
FOLLOW UP
WITH THE REFERENCES AS WELL AS THE FOLLOWING FIVE BOOKS COVERING THE
RELEVANT TOPIC:
1. MUNDY, B. R.; ELLERD, M. G.
NAME REACTIONS AND REAGENTS IN ORGANIC SYN
THESIS JOHN
YY
WILEY & SONS, NEW YORK, 1988.
2. HASSNER, A.; STUMER, C.
ORGANIC SYNTHESIS BASED ON NAMED AND UNNAMED
REACTIONS PERGAMON, 1994.
3. LAUE, L.; PLAGENS, A.
NAMED ORGANIC REACTIONS JOHN
YY
WILEY & SONS, NEW
YORK, 1999.
4. "ORGANIC NAME REACTIONS" SECTION,
THE MERCK INDEX (13
TH
EDITION),
2001.
5. SMITH, M. B.; MARCH, J. "ADVANCED ORGANIC CHEMISTRY" (5
TH
EDITION), WILEY,
NEW YORK, 2001.
I WOULD LIKE TO EXPRESS MY GRATEFUL THANKS TO DR. BRIAN J. MYERS OF
WAYNE
SATE UNIVERSITY, PROFS. JEFFREY N. JOHNSTON OF INDIANA UNIVERSITY AND
CHRISTIAN M.
ROJAS OF BERNARD COLLEGE, WHO READ THE MANUSCRIPT AND OFFERED MANY
INVALUABLE
COMMENTS AND SUGGESTIONS. SPECIAL THANKS ARE DUE TO PROFS. GORDON W.
GRIBBLE
OF DARTMOUTH COLLEGE, LOUIS S. HEGEDUS OF COLORADO STATE UNIVERSITY, AND
THO
MAS R. HOYE OF UNIVERSITY OF MINNESOTA FOR THEIR CRITIQUE OF THE DRAFTS.
IN ADDI
TION, I AM VERY MUCH INDEBTED TO NADIA M. AHMAD, JOHN (JACK) HODGES,
MICHAEL
D. KAUFMAN, PETER L TOOGOOD, AND KIM E. WERNER FOR PROOFREADING THE MANU
SCRIPT. ANY REMAINING ERRORS ARE, OF COURSE, SOLELY MY OWN. I AM ALSO
GRATEFUL TO
MS. ANN SMITH OF MERCK & CO., INC. FOR HER HELPFUL COMMUNICATIONS AND
DISCUS
SIONS. LAST BUT NOT THE LEAST, I WISH TO THANK MY WIFE, SHERRY CHUN-HUA
CAI, FOR
HER UNDERSTANDING AND SUPPORT THROUGHOUT THE ENTIRE PROJECT.
JACK LI
ANN ARBOR, MICHIGAN
NOVEMBER, 2001
REFERENCES
A. WILLIAM SHAKESPEARE, "ROMEO AND JULIET" ACT II, SCENE II,
1594
YY
YY
YY
YY
1595.
B. DEREK H. R. BARTON, "SOME RECOLLECTIONS OF GAP JUMPING" AMERICAN
CHEMICAL SOCIETY, WASHINGTON, DC,
1991. |
| any_adam_object | 1 |
| author | Li, Jie Jack 1964- |
| author_GND | (DE-588)123481848 |
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| author_role | aut |
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| classification_tum | CHE 608b CHE 620b |
| ctrlnum | (OCoLC)49238689 (DE-599)BVBBV014112076 |
| dewey-full | 547/.2 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547/.2 |
| dewey-search | 547/.2 |
| dewey-sort | 3547 12 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Chemie |
| format | Book |
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| id | DE-604.BV014112076 |
| illustrated | Illustrated |
| indexdate | 2025-02-03T11:03:03Z |
| institution | BVB |
| isbn | 3540430245 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-009668946 |
| oclc_num | 49238689 |
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| physical | XVIII, 416 S. graph. Darst. |
| publishDate | 2002 |
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| publisher | Springer |
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| spelling | Li, Jie Jack 1964- Verfasser (DE-588)123481848 aut Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] Jie Jack Li Berlin [u.a.] Springer 2002 XVIII, 416 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Chimie organique Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Reaktionsmechanismus (DE-588)4177123-0 gnd rswk-swf Namensreaktion (DE-588)4171139-7 gnd rswk-swf Organische Chemie (DE-588)4043793-0 gnd rswk-swf 1\p (DE-588)4066724-8 Wörterbuch gnd-content Namensreaktion (DE-588)4171139-7 s Reaktionsmechanismus (DE-588)4177123-0 s DE-604 Organische Chemie (DE-588)4043793-0 s 2\p DE-604 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009668946&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Li, Jie Jack 1964- Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] Chimie organique Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd |
| subject_GND | (DE-588)4177123-0 (DE-588)4171139-7 (DE-588)4043793-0 (DE-588)4066724-8 |
| title | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] |
| title_auth | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] |
| title_exact_search | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] |
| title_full | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] Jie Jack Li |
| title_fullStr | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] Jie Jack Li |
| title_full_unstemmed | Name reactions a collection of detailed reaction mechanisms ; [more than 300 reactions] Jie Jack Li |
| title_short | Name reactions |
| title_sort | name reactions a collection of detailed reaction mechanisms more than 300 reactions |
| title_sub | a collection of detailed reaction mechanisms ; [more than 300 reactions] |
| topic | Chimie organique Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd |
| topic_facet | Chimie organique Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Reaktionsmechanismus Namensreaktion Organische Chemie Wörterbuch |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009668946&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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