Name reactions : a collection of detailed reaction mechanisms /
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| Author / Creator: | Li, Jie Jack. |
|---|---|
| Imprint: | Berlin ; New York : Springer, c2002. |
| Description: | xviii, 416 p. : ill. ; 24 cm. |
| Language: | English |
| Subject: | |
| Format: | Print Book |
| URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/4699207 |
Table of Contents:
- Preface
- Abbreviations
- 1. Abnormal Claisen rearrangement
- 2. Alder ene reaction
- 3. Allan-Robinson reaction
- 4. Alper carbonylation
- 5. Amadori glucosamine rearrangement
- 6. Angeli-Rimini hydroxamic acid synthesis
- 7. ANRORC mechanism
- 8. Arndt-Eistert homologation
- 9. Baeyer-Drewson indigo synthesis
- 10. Baeyer-Villiger oxidation
- 11. Baker-Venkataraman rearrangement
- 12. Bamberger rearrangement
- 13. Bamford-Stevens reaction
- 14. Bargellini reaction
- 15. Bartoli indole synthesis
- 16. Barton decarboxylation
- 17. Barton-McCombie deoxygenation
- 18. Barton nitrite photolysis
- 19. Baylis-Hillman reaction
- 20. Beckmann rearrangement
- 21. Beirut reaction
- 22. Benzilic acid rearrangement
- 23. Benzoin condensation
- 24. Bergman cyclization
- 25. Biginelli pyrimidone synthesis
- 26. Birch reduction
- 27. Bischler-Möhlau indole synthesis
- 28. Bischler-Napieralski reaction
- 29. Blaise reaction
- 30. Blanc chloromethylation reaction
- 31. Boekelheide reaction
- 32. Boger pyridine synthesis
- 33. Boord reaction
- 34. Borsche-Drechsel cyclization
- 35. Boulton-Katritzky rearrangement
- 36. Bouveault aldehyde synthesis
- 37. Bouveault-Blanc reduction
- 38. Boyland-Sims oxidation
- 39. Bradsher reaction
- 40. Brook rearrangement
- 41. Brown hydroboration reaction
- 42. Bucherer carbazole synthesis
- 43. Bucherer reaction
- 44. Bucherer-Bergs reaction
- 45. Buchner-Curtius-Schlotterbeck reaction
- 46. Buchner method of ring expansion
- 47. Buchwald-Hartwig C-N bond and C-O bond formation reactions
- 48. Burgess dehydrating reagent
- 49. Cadiot-Chodkiewicz coupling
- 50. Cannizzaro dispropotionation reaction
- 51. Carroll rearrangement
- 52. Castro-Stephens coupling
- 53. Chapman rearrangement
- 54. Chichibabin amination reaction
- 55. Chichibabin pyridine synthesis
- 56. Chugaev reaction
- 57. Ciamician-Dennsted rearrangement
- 58. Claisen, Eschenmoser-Claisen, Johnson-Claisenand, and Ireland-Claisen rearrangements
- 59. Clark-Eschweiler reductive alkylation of amines
- 60. Combes quinoline synthesis
- 61. Conrad-Lipach reaction
- 62. Cope elimination reaction
- 63. Cope, oxy-Cope, and anionic oxy-Cope rearrangements
- 64. Corey-Chaykovsky epoxidation
- 65. Corey-Fuchs reaction
- 66. Corey-Bakshi-Shibata (CBS) reduction
- 67. Corey-Kim oxidation
- 68. Corey-Winter olefin synthesis
- 69. Cornforth rearrangement
- 70. Criegee glycol cleavage
- 71. Criegee mechanism of ozonolysis
- 72. Curtius rearrangement
- 73. Dakin reaction
- 74. Dakin-West reaction
- 75. Danheiser annulation
- 76. Darzens glycidic ester condensation
- 77. Davis chiral oxaziridine reagent
- 78. de Mayo reaction
- 79. Demj anov rearrangement
- 80. Dess-Martin periodinane oxidation
- 81. Dieckmann condensation
- 82. Diels-Alder reaction, reverse electronic demand Diels-Alder reaction, hetero-Diels-Alder reaction
- 83. Dienone-phenol rearrangement
- 84. Di-¿-methane rearrangement
- 85. Doebner reaction
- 86. Doebner-von Miller reaction
- 87. Doering-LaFlamme allene synthesis
- 88. Dornow-Wiehler isoxazole synthesis
- 89. Dötz reaction
- 90. Dutt-Wormall reaction
- 91. Eschenmoser coupling reaction
- 92. Eschenmoser-Tanabe fragmentation
- 93. Étard reaction
- 94. Evans aldol reaction
- 95. Favorskii rearrangement and Quasi-Favorskii rearrangement
- 96. Feist-Bénary furan synthesis
- 97. Ferrier rearrangement
- 98. Fischer-Hepp rearrangement
- 99. Fischer indole synthesis
- 100. Fischer-Speier esterification
- 101. Fleming oxidation
- 102. Forster reaction
- 103. Frater-Seebach alkylation
- 104. Friedel-Crafts reaction
- 105. Friedländer synthesis
- 106. Fries rearrangement
- 107. Fritsch-Buttenberg-Wiechell rearrangement
- 108. Fujimoto-Belleau reaction
- 109. Fukuyama amine synthesis
- 110. Gabriel synthesis
- 111. Gassman indole synthesis
- 112. Gattermann-Koch reaction
- 113. Gewald aminothiophene synthesis
- 114. Glaser coupling
- 115. Gomberg-Bachmann reaction
- 116. Gribble indole reduction
- 117. Gribble reduction of diaryl ketones
- 118. Grob fragmentation
- 119. Guareschi-Thorpe condensation
- 120. Hajos-Wiechert reaction
- 121. Haller-Bauer reaction
- 122. Hantzsch pyridine synthesis
- 123. Hantzsch pyrrole synthesis
- 124. Haworth reaction
- 125. Hayashi rearrangement
- 126. Heck reaction
- 127. Hegedus indole synthesis
- 128. Hell-Volhardt-Zelinsky reaction
- 129. Henry reaction (nitroaldol reaction)
- 130. Herz reaction
- 131. Heteroaryl Heck reaction
- 132. Hiyama cross-coupling reaction
- 133. Hodges-Vedejs metallation of oxazoles
- 134. Hofmann rearrangement (Hofmann degradation reaction)
- 135. Hofmann-Loffler-Freytag reaction
- 136. Hofmann-Martius reaction (Reilly-Hickinbottom rearrangement)
- 137. Hooker oxidation
- 138. Horner-Wadsworth-Emmons reaction
- 139. Houben-Hoesch synthesis
- 140. Hunsdiecker reaction
- 141. Ing-Manske procedure
- 142. Jacobsen-Katsuki epoxidation
- 143. Jacobsen rearrangement
- 144. Japp-Klingemann hydrazone synthesis
- 145. Julia-Lythgoe olefination
- 146. Kahne glycosidation
- 147. Keck stereoselective allylation
- 148. Keck macrolactonization
- 149. Kemp elimination
- 150. Kennedy oxidative cyclization
- 151. Kharasch addition reaction
- 152. Knoevenagel condensation
- 153. Knorr pyrrole synthesis
- 154. Koch carbonylation reaction (Koch-Haaf carbonylation reaction)
- 155. Koenigs-Knorr glycosidation
- 156. Kolbe-Schmitt reaction
- 157. Kostanecki reaction
- 158. Krapcho decarboxylation
- 159. Kröhnke reaction (pyridine synthesis)
- 160. Kumada cross-coupling reaction
- 161. Larock indole synthesis
- 162. Lawesson's reagent
- 163. Leuckart-Wallach reaction
- 164. Lieben haloform reaction
- 165. Liebeskind-Srogl coupling
- 166. Lossen rearrangement
- 167. Luche reduction
- 168. McFadyen-Stevens reduction
- 169. McLafferty rearrangement
- 170. McMurry coupling
- 171. Madelung indole synthesis
- 172. Mannich reaction
- 173. Marshall boronate fragmentation
- 174. Martin's sulfurane dehydrating reagent
- 175. Masamune-Roush conditions
- 176. Meerwein arylation
- 177. Meerwein-Ponndorf-Verley reduction
- 178. Meinwald rearrangement
- 179. Meisenheimer complex
- 180. Meisenheimer rearrangement
- 181. Meyer-Schuster rearrangement
- 182. Michael addition
- 183. Michaelis-Arbuzov phosphonate synthesis
- 184. Midland reduction
- 185. Miller-Snyder aryl cyanide synthesis
- 186. Mislow-Evans rearrangement
- 187. Mitsunobu reaction
- 188. Miyaura boration reaction
- 189. Moffatt oxidation
- 190. Morgan-Walls reaction (Pictet-Hubert reaction)
- 191. Mori-Ban indole synthesis
- 192. Morin rearrangement
- 193. Mukaiyama aldol reaction
- 194. Mukaiyama esterification
- 195. Myers-Saito cyclization
- 196. Nametkin rearrangement (retropinacol rearrangement)
- 197. Nazarov cyclization
- 198. Neber rearrangement
- 199. Nef reaction
- 200. Negishi cross-coupling reaction
- 201. Nenitzescu indole synthesis
- 202. Nicholas reaction
- 203. Noyori asymmetric hydrogenation
- 204. Nozaki-Hiyama-Kishi reaction
- 205. Oppenauer oxidation
- 206. Orton rearrangement
- 207. Overman rearrangement
- 208. Paal-Knorr furan synthesis
- 209. Paal-Knorr pyrrole synthesis
- 210. Parham cyclization
- 211. Passerini reaction
- 212. Paterno-Büchi reaction
- 213. Pauson-Khand cyclopentenone synthesis
- 214. Payne rearrangement
- 215. Pechmann condensation (coumarin synthesis)
- 216. Pechmann pyrazole synthesis
- 217. Perkin reaction (cinnamic acid synthesis)
- 218. Perkow vinyl phosphate synthesis
- 219. Peterson olefination
- 220. Pfau-Plattner azulene synthesis
- 221. Pfitzinger quinoline synthesis
- 222. Pictet-Gams isoquinoline synthesis
- 223. Pictet-Spengler isoquinoline synthesis
- 224. Pinacol rearrangement
- 225. Pinner synthesis
- 226. Polonovski reaction
- 227. Polonovski-Potier rearrangement
- 228. Pomeranz-Fritsch reaction
- 229. Préost /raws-dihydroxylation
- 230. Prilezhaev reaction
- 231. Prins reaction
- 232. Pschorr ring closure
- 233. Pummerer rearrangement
- 234. Ramberg-Bäcklund olefin synthesis
- 235. Reformatsky reaction
- 236. Regitz diazo synthesis
- 237. Reimer-Tiemann reaction
- 238. Reissert reaction (aldehyde synthesis)
- 239. Riley oxidation (selenium dioxide oxidation)
- 240. Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts
- 241. Ritter reaction
- 242. Robinson annulation
- 243. Robinson-Schöpf reaction
- 244. Roush allylboronate reagent
- 245. Rubottom oxidation
- 246. Rupe rearrangement
- 247. Rychnovsky polyol synthesis
- 248. Sakurai allylation reaction (Hosomi-Sakurai reaction)
- 249. Sandmeyer reaction
- 250. Sarett oxidation
- 251. Schiemann reaction (Balz-Schiemann reaction)
- 252. Schlosser modification of the Wittig reaction
- 253. Schmidt reaction
- 254. Schmidt's trichloroacetimidate glycosidation reaction
- 255. Scholl reaction
- 256. Schöpf reaction
- 257. Schotten-Baumann reaction
- 258. Shapiro reaction
- 259. Sharpless asymmetric aminohydroxylation
- 260. Sharpless asymmetric epoxidation
- 261. Sharpless dihydroxylation
- 262. Shi asymmetric epoxidation
- 263. Simmons-Smith reaction
- 264. Simonini reaction
- 265. Simonis chromone cyclization
- 266. Skraup quinoline synthesis
- 267. Smiles rearrangement
- 268. Sommelet reaction
- 269. Sommelet-Hauser (ammonium ylide) rearrangement
- 270. Sonogashira reaction
- 271. Staudinger reaction
- 272. Stetter reaction (Michael-Stetter reaction)
- 273. Stevens rearrangement
- 274. Stieglitz rearrangement
- 275. Still-Gennari phosphonate reaction
- 276. Stille coupling
- 277. Stille-Kelly reaction
- 278. Stobbe condensation
- 279. Stollé synthesis
- 280. Stork enamine reaction
- 281. Strecker amino acid synthesis
- 282. Suzuki coupling
- 283. Swern oxidation
- 284. Tamao-Kumada oxidation
- 285. Tebbe olefination (Petasis alkenylation)
- 286. Thorpe-Ziegler reaction
- 287. Tiemann rearrangement
- 288. Tiffeneau-Demjanov rearrangement
- 289. Tishchenko reaction
- 290. Tollens reaction
- 291. Tsuji-Trost allylation
- 292. Ueno-Stork cyclization
- 293. Ugi reaction
- 294. Ullmann reaction
- 295. Vilsmeier-Haack reaction
- 296. von Braun reaction
- 297. von Richter reaction
- 298. Wacker oxidation
- 299. Wagner-Meerwein rearrangement
- 300. Wallach rearrangement
- 301. Weinreb amide
- 302. Weiss reaction
- 303. Wharton oxygen transposition reaction
- 304. Willgerodt-Kindler reaction
- 305. Wittig reaction
- 306. [1,2]-Wittig rearrangement
- 307. [2,3]-Wittig rearrangement
- 308. Wohl-Ziegler reaction
- 309. Wolff rearrangement
- 310. Wolff-Kishner reduction
- 311. Woodward c/'s-dihydroxylation
- 312. Yamada coupling reagent
- 313. Yamaguchi esterification
- 314. Zaitsev elimination
- 315. Zinin benzidine rearrangement (semidine rearrangement)
- Subject Index
