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| Abbreviations | XVII | ||
| 1. Abnormal Claisen rearrangement | i | ||
| 2. Alder ene reaction | |||
| 3. Aldol condensation | 3 | (1) | |
| 4. Allan-Robinson reaction | 4 | (2) | |
| 5. Alper carbonylation | 6 | (2) | |
| 6. Amadori rearrangement | 8 | (1) | |
| 7. Angeli-Rimini hydroxamic acid synthesis | 9 | (1) | |
| 8. ANRORC mechanism | 10 | (1) | |
| 9. Arndt-Eistert homologation | 11 | (2) | |
| 10. Auwers reaction | 13 | (1) | |
| 11. Baeyer-Drewson indigo synthesis | 14 | (2) | |
| 12. Baeyer-Villiger oxidation | 16 | (1) | |
| 13. Baker-Venkataraman rearrangement | 17 | (1) | |
| 14. Bamberger rearrangement | 18 | (1) | |
| 15. Bamford-Stevens reaction | 19 | (1) | |
| 16. Bargellini reaction | 20 | (1) | |
| 17. Bartoli indole synthesis | 21 | (1) | |
| 18. Barton decarboxylation | 22 | (1) | |
| 19. Barton-McCombie deoxygenation | 23 | (1) | |
| 20. Barton nitrite photolysis | 24 | (2) | |
| 21. Bayhs-Hillman reaction | 26 | (2) | |
| 22. Beckmann rearrangement | 28 | (1) | |
| 23. Beirut reaction. | 29 | (2) | |
| 24. Benzilic acid rearrangement | 31 | (1) | |
| 25. Benzoincondensation | 32 | (1) | |
| 26. Bergman cyclization | 33 | (1) | |
| 27. Biginelli pyrimidone synthesis | 34 | (2) | |
| 28. Birch reduction | 36 | (2) | |
| 29. Bischler-Möhlau indole synthesis | 38 | (1) | |
| 30. Bischler-Napieralski reaction | 39 | (1) | |
| 31. Blaise reaction, | 40 | (1) | |
| 32. Blanc chloromethylation reaction | 41 | (1) | |
| 33. Boekelheide reaction | 42 | (1) | |
| 34. Boger pyridine synthesis | 43 | (1) | |
| 35. Boord reaction | 44 | (1) | |
| 36. Borsche-Drechsel cyclization | 45 | (2) | |
| 37. Boulton-Katritzky rearrangement | |||
| 38. Bouveault aldehyde synthesis | 47 | (1) | |
| 39. Bouveault-Blanc reduction | 48 | (1) | |
| 40. Boyland-Sims oxidation | 49 | (2) | |
| 41. Bradsher reaction | 51 | (1) | |
| 42. Brook rearrangement | 52 | (1) | |
| 43. Brown hydroboration reaction | 53 | (1) | |
| 44. Bucherer carbazole synthesis | 54 | (2) | |
| 45. Bucherer reaction | 56 | (1) | |
| 46. Bucherer-Bergs reaction | 57 | (1) | |
| 47. Buchner-Curtius-Schlotterbeck reaction | 58 | (1) | |
| 48. Buchner method of ring expansion | 59 | (1) | |
| 49. Buchwald-Hartwig C-N bond and C-O bond formation reactions | 60 | (1) | |
| 50. Burgess dehydrating reagent | 61 | (1) | |
| 51. Cadiot--Chodkiewicz coupling | 62 | (1) | |
| 52. Cannizzaro dispropotionation reaction | 63 | (2) | |
| 53. Carroll rearrangement | 65 | (1) | |
| 54. Castro-Stephens coupling | 66 | (1) | |
| 55. Chapman rearrangement | 67 | (1) | |
| 56. Chichibabin amination reaction | 68 | (1) | |
| 57. Chichibabin pyridine synthesis | 69 | (2) | |
| 58. Chugaev reaction | 71 | (1) | |
| 59. Ciamician-Dennsted rearrangement | 72 | (1) | |
| 60. Claisen condensation | 73 | (1) | |
| 61. Claisen rearrangement | 74 | (2) | |
| 62. Clarke-Eschweiler reductive alkylation of amines | 76 | (1) | |
| 63. Clemmensen reduction | 77 | (2) | |
| 64. Combes quinoline synthesis | 79 | (2) | |
| 65. Conrad-Limpach reaction | 81 | (1) | |
| 66. Cook-Heilbron thiazole synthesis | 82 | (1) | |
| 67. Cope elimination reaction | 83 | (1) | |
| 68. Cope, oxy-Cope, and anionic oxy-Cope rearrangements | 84 | (2) | |
| 69. Corey-Bakshi-Shibata (CBS) reduction | 86 | (2) | |
| 70. Corey-Chaykovsky reaction | 88 | (2) | |
| 71. Corey-Fuchs reaction | 90 | (2) | |
| 72. Corey-Kim oxidation | 92 | (1) | |
| 73. Corey-Winter olefin synthesis | 93 | (2) | |
| 74. Cornforth rearrangement | 95 | (1) | |
| 75. Criegee glycol cleavage | 96 | (1) | |
| 76. Criegee mechanism of ozonolysis | 97 | (1) | |
| 71. Curtius rearrangement | 98 | (1) | |
| 78. Dakin oxidation, | 99 | (1) | |
| 79. Dakin-West reaction | 100 | (2) | |
| 80. Danheiser annulation | 102 | (1) | |
| 81. Darzens glycidic ester condensation | 103 | (1) | |
| 82. Davis chiral oxaziridine reagent | 104 | (1) | |
| 83. de Mayo reaction | 105 | (2) | |
| 84. Demjanov rearrangement | 107 | (2) | |
| 85. Dess-Martin periodinane oxidation | 109 | (1) | |
| 86. Dieckmann condensation | 110 | (1) | |
| 87. Diels-Alder reaction | 111 | (2) | |
| 88. Dienone-phenol rearrangement | 113 | (1) | |
| 89. Di-it-methane rearrangement | 114 | (1) | |
| 90. Doebner reaction | 115 | (2) | |
| 91. Doebner-von Miller reaction | 117 | (2) | |
| 92. Doering-LaFlamme allene synthesis | 119 | (1) | |
| 93. Dornow-Wiehler isoxazole synthesis | 120 | (2) | |
| 94. Dötz reaction | 122 | (1) | |
| 95. Dowd ring expansion | 123 | (2) | |
| 96. Dutt-Wormall reaction | 125 | (1) | |
| 97. Eglinton reaction | 126 | (1) | |
| 98. Eschenmoser coupling reaction | 127 | (1) | |
| 99. Eschenmoser-Tanabe fragmentation | 128 | (1) | |
| 100. Etard reaction | 129 | (1) | |
| 101. Evans aldol reaction | 130 | (2) | |
| 102. Favorskii rearrangement and Quasi-Favorskii rearrangement | 132 | (2) | |
| 103. Feist-Bénary furan synthesis | 134 | (1) | |
| 104. Ferrier rearrangement | 135 | (1) | |
| 105. Finkelstein reaction | 136 | (1) | |
| 106. Fischer-Hepp rearrangement | 137 | (1) | |
| 107. Fischer indole synthesis | 138 | (1) | |
| 108. Fischer-Speier esterification | 139 | (1) | |
| 109. Fleming oxidation | 140 | (2) | |
| 110. Forster reaction | 142 | (2) | |
| 111. Frater-Seebach alkylation | 144 | (1) | |
| 112. Friedel-Crafts reaction | 145 | (2) | |
| 113. Friedländer synthesis | 147 | (2) | |
| 114. Fries rearrangement | 149 | (2) | |
| 115. Fritsch-Buttenberg-Wiechell rearrangement | 151 | (1) | |
| 116. Fujimoto-Belleau reaction | 152 | (1) | |
| 117. Fukuyama amine synthesis | 153 | (2) | |
| 118. Gabriel synthesis | 155 | (1) | |
| 119. Gassman indole synthesis | 156 | (1) | |
| 120. Gattermann-Koch reaction | 157 | (1) | |
| 121. Gewald aminothiophene synthesis | 158 | (2) | |
| 122. Glaser coupling | 160 | (1) | |
| 123. Gomberg-Bachmann reaction | 161 | (1) | |
| 124. Gribble indole reduction | 162 | (1) | |
| 125. Gribble reduction of diaryl ketones | 163 | (1) | |
| 126. Grignard reaction | 164 | (2) | |
| 127. Grob fragmentation | 166 | (2) | |
| 128. Guareschi-Thorpe condensation | 168 | (1) | |
| 129. Hajos-Wiechert reaction | 169 | (2) | |
| 130. Haller-Bauer reaction | 171 | (1) | |
| 131. Hantzsch pyridine synthesis | 172 | (2) | |
| 132. Hantzsch pyrrole synthesis | 174 | ||
| 133. Haworth reaction | 115 | (62) | |
| 134. Hayashi rearrangement | 177 | (2) | |
| 135. Heck reaction | 179 | (2) | |
| 136. Hegedus indole synthesis | 181 | (1) | |
| 137. Hell-Volhardt-Zelinsky reaction | 182 | (1) | |
| 138. Henry reaction (nitroaldol reaction) | 183 | (1) | |
| 139. Herz reaction | 184 | (2) | |
| 140. Heteroaryl Heck reaction | 186 | (1) | |
| 141. Hiyama cross-coupling reaction | 187 | (2) | |
| 142. Hoch-Campbell aziridine synthesis | 189 | (2) | |
| 143. Hodges-Vedejs metallation of oxazoles | 191 | (1) | |
| 144. Hofmann rearrangement (Hofmann degradation reaction) | 192 | (1) | |
| 145. Hofmann-Löffler-Freytag reaction | 193 | (1) | |
| 146. Hofmann-Martius reaction (Reilly-Hickinbottom rearrangement) | 194 | (2) | |
| 147. Hooker oxidation | 196 | (2) | |
| 148. Horner-Wadsworth-Emmons reaction | 198 | (2) | |
| 149. Houben-Hoesch synthesis | 200 | (2) | |
| 150. Hunsdiecker reaction | 202 | (1) | |
| 151. Ing-Manske procedure | 203 | (1) | |
| 152. Jacobsen-Katsuki epoxidation | 204 | (2) | |
| 153. Jacobsen rearrangement | 206 | (2) | |
| 154. Japp-Klingemann hydrazone synthesis | 208 | (1) | |
| 155. Julia-Lythgoe olefination | 209 | (2) | |
| 156. Kahne glycosidation | 211 | (2) | |
| 157. Keck stereoselective allylation | 213 | (2) | |
| 158. Keck macrolactonization | 215 | (2) | |
| 159. Kemp elimination | 217 | (1) | |
| 160. Kennedy oxidative cyclization | 218 | (1) | |
| 161. Kharasch addition reaction | 219 | (1) | |
| 162. Knöevenagel condensation | 220 | (2) | |
| 163. Knorr pyrrole synthesis | 222 | (1) | |
| 164. Koch carbonylation reaction (Koch-Haaf carbonylation reaction) | 223 | (2) | |
| 165. Koenig-Knorr glycosidation | 225 | (1) | |
| 166. Kolbe electrolytic coupling | 226 | (1) | |
| 167. Kolbe-Schmitt reaction | 227 | (1) | |
| 168. Kostanecki reaction | 228 | (2) | |
| 169. Krapcho decarboxylation | 230 | (1) | |
| 170. Kröhnke reaction (pyridine synthesis) | 231 | (2) | |
| 171. Kumafia cross-coupling reaction | 233 | (2) | |
| 172. Larock indole synthesis | 235 | (1) | |
| 173. Lawesson's reagent | 236 | (1) | |
| 174. Leuckart-Wallach reaction | 237 | (1) | |
| 175. Lieben haloform reaction | 238 | (1) | |
| 176. Liebeskind-Srogl coupling | 239 | (1) | |
| 177. Lossen rearrangement | 240 | (1) | |
| 178. Luche reduction | 241 | (1) | |
| 179. McFadyen-Stevens reduction | 242 | (1) | |
| 180. McLafferty rearrangement | 243 | (1) | |
| 181. McMurry coupling | 244 | (1) | |
| 182. Madelung indole synthesis | 245 | (1) | |
| 183. Mannich reaction | 246 | (2) | |
| 184. Marshall boronate fragmentation | 248 | (1) | |
| 185. Martin's sulfurane dehydrating reagent | 249 | (2) | |
| 186. Masamune-Roush conditions | 251 | (2) | |
| 187. Meerwein arylation | 253 | (1) | |
| 188. Meerwein-Ponndorf-Verley reduction | 254 | (1) | |
| 189. Meinwald rearrangement | 255 | (1) | |
| 190. Meisenheimer complex | 256 | (2) | |
| 191. Meisenheimer rearrangement | 258 | (1) | |
| 192. Meyer-Schuster rearrangement | 259 | (1) | |
| 193. Michael addition | 260 | (1) | |
| 194. Michaelis-Arbuzov phosphonate synthesis | 261 | (1) | |
| 195. Midland reduction | 262 | (1) | |
| 196. Miller-Loudon-Snyder nitrile synthesis | 263 | (1) | |
| 191. Mislow-Evans rearrangement | 264 | (1) | |
| 198. Mitsunobu reaction | 265 | (1) | |
| 199. Miyaura boration reaction | 266 | (1) | |
| 200. Moffatt oxidation | 267 | (2) | |
| 201. Morgan-Walls reaction (Pictet-Hubert reaction) | 269 | (1) | |
| 202. Mori-Ban indole synthesis | 270 | (2) | |
| 203. Morin rearrangement | 272 | (2) | |
| 204. Mukaiyama aldol reaction | 274 | ||
| 205. Mukaiyama esterification | 215 | (62) | |
| 206. Myers-Saito cyclization | 277 | (2) | |
| 207. Nametkin rearrangement (retropinacol rearrangement) | 279 | (1) | |
| 208. Nazarov cyclization | 280 | (1) | |
| 209. Neber rearrangement | 281 | (1) | |
| 210. Nef reaction | 282 | (1) | |
| 211. Negishi cross-coupling reaction | 283 | (1) | |
| 212. Nenitzescu indole synthesis | 284 | (2) | |
| 213. Nicholas reaction | 286 | (1) | |
| 214. Noyori asymmetric hydrogenation | 287 | (2) | |
| 215. Nozaki-Hiyama-Kishi reaction | 289 | (1) | |
| 216. Oppenauer oxidation | 290 | (1) | |
| 217. Orton rearrangement | 291 | (2) | |
| 218. Overman rearrangement | 293 | (1) | |
| 219. Paal-Knorr furan synthesis | 294 | (1) | |
| 220. Paal-Knorr pyrrole synthesis | 295 | (1) | |
| 221. Parham cyclization | 296 | (2) | |
| 222. Passerine reaction | 298 | (1) | |
| 223. Paterno-Büchi reaction | 299 | (1) | |
| 224. Pauson-Khand cyclopentenone synthesis | 300 | (2) | |
| 225. Payne rearrangement | 302 | (1) | |
| 226. Pechmann condensation (coumarin synthesis) | 303 | (1) | |
| 227. Pechmann pyrazole synthesis | 304 | (1) | |
| 228. Perkin reaction (cinnamic acid synthesis) | 305 | (2) | |
| 229. Perkow vinyl phosphate synthesis | 307 | (1) | |
| 230. Peterson olefination | 308 | (2) | |
| 231. Pfau-Plattuer azunene synthesis | 310 | (1) | |
| 232. Pfitzinger quinoline synthesis | 311 | (1) | |
| 233. Pictet-Gams isoquinoline synthesis | 312 | (2) | |
| 234. Pictet-Spengler tetrahydroisoquinoline synthesis | 314 | (1) | |
| 235. Pinacol rearrangement | 315 | (1) | |
| 236. Pinner synthesis | 316 | (1) | |
| 237. Polonovski reaction | 317 | (2) | |
| 238. Polonovski-Potier rearrangement | 319 | (1) | |
| 239. Pomeranz-Fritsch reaction | 320 | (2) | |
| 240. Prévost trans-dihydroxylation | 322 | (1) | |
| 241. Prilezhaev reaction | 323 | (1) | |
| 242. Prins reaction | 324 | (1) | |
| 243. Pschorr ring closure | 325 | (2) | |
| 244. Pummerer rearrangement | 327 | (1) | |
| 245. Ramberg-Bäcklund olefin synthesis | 328 | (1) | |
| 246. Reformatsky reaction | 329 | (1) | |
| 247. Regitz diazo synthesis | 330 | (2) | |
| 248. Reimer-Tiemann reaction | 332 | (2) | |
| 249. Reissers reaction (aldehyde synthesis) | 334 | (2) | |
| 250. Riley oxidation (selenium dioxide oxidation) | 336 | (1) | |
| 251. Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts | 337 | (2) | |
| 252. Ritter reaction | 339 | (1) | |
| 253. Robinson annulation | 340 | (1) | |
| 254. Robinson-Schöpf reaction | 341 | (2) | |
| 255. Rosenmund reduction | 343 | (1) | |
| 256. Roush allylboronate reagent | 344 | (1) | |
| 257. Rubottom oxidation | 345 | (1) | |
| 258. Rupe rearrangement | 346 | (1) | |
| 259. Rychnovsky polyol synthesis | 347 | (2) | |
| 260. Sakurai allylation reaction (Hosomi-Sakurai reaction) | 349 | (2) | |
| 261. Sandmeyer reaction | 351 | (1) | |
| 262. Sarett oxidation | 352 | (2) | |
| 263. Schiemann reaction (Balz-Schiemann reaction) | 354 | (1) | |
| 264. Schlosser modification of the Wittig reaction | 355 | (1) | |
| 265. Schmidt reaction | 356 | (1) | |
| 266. Schmidt's trichloroacetimidate glycosidation reaction | 357 | (2) | |
| 267. Schonl reaction | 359 | (2) | |
| 268. Schöpf reaction | 361 | (1) | |
| 269. Schotten-Baumann reaction | 362 | (1) | |
| 270. Shapiro reaction | 363 | (1) | |
| 271. Sharpless asymmetric amino hydroxylation | 364 | (2) | |
| 272. Sharpless asymmetric epoxidation | 366 | (3) | |
| 273. Sharpless dihydroxylation | 369 | (3) | |
| 274. Shi asymmetric epoxidation | 372 | (2) | |
| 275. Simmons-Smith reaction | 374 | (1) | |
| 276. Simonini reaction | 375 | (1) | |
| 277. Simonis chromone cyclization | 376 | (2) | |
| 278. Skraup quinoline synthesis | 378 | (2) | |
| 279. Smiles rearrangement | 380 | (1) | |
| 280. Sommelet reaction | 381 | (2) | |
| 281. Sommelet-Hauser (ammonium ylide) rearrangement | 383 | (1) | |
| 282. Sonogashira reaction | 384 | (2) | |
| 283. Staudinger reaction | 386 | (1) | |
| 284. Stetter reaction (Michael-Stetter reaction) | 387 | (2) | |
| 285. Stevens rearrangement | 389 | (2) | |
| 286. Stieglitz rearrangement | 391 | (1) | |
| 287. Still-Gennari phosphonate reaction | 392 | (1) | |
| 288. Stille coupling | 393 | (1) | |
| 289. Stille-Kelly reaction | 394 | (2) | |
| 290. Stobbe condensation | 396 | (1) | |
| 291. Stolle synthesis | 397 | (1) | |
| 292. Stork mamine reaction | 398 | (1) | |
| 293. Strecker amino acid synthesis | 399 | (2) | |
| 294. Suzuki coupling | 401 | (1) | |
| 295 Swern oxidation | 402 | (2) | |
| 296. Tamso-Kumafia oxidation | 404 | (1) | |
| 297. Tebbe olefination (Petasis alkenylation) | 405 | (2) | |
| 298. Thorpe-Ziegler reaction | 407 | (1) | |
| 299. Tiemann rearrangement | 408 | (1) | |
| 300. Tiffeneau-Demjanov rearrangement | 409 | (2) | |
| 301. Tishchenko reaction | 411 | (1) | |
| 302. Tollens reaction | 412 | (2) | |
| 303. Tsuji-Trost a11ylation | 414 | (1) | |
| 304. Ueno-Stork cyclization | 415 | (1) | |
| 305. Ugi reaction | 416 | (2) | |
| 306. Ullmann reaction | 418 | (1) | |
| 307. Vilsmeier-Haack reaction | 419 | (2) | |
| 308. von Braun reaction | 421 | (1) | |
| 309. von Richter reaction | 422 | (2) | |
| 310. Wacker oxidation | 424 | (2) | |
| 311. Wagner-Meerwein rearrangement | 426 | (1) | |
| 312. Wallach rearrangement | 427 | (1) | |
| 313. Weinreb amide | 428 | (1) | |
| 314. Weiss reaction | 429 | (2) | |
| 315. Wenker aziridine synthesis | 431 | (2) | |
| 316. Wharton oxygen transposition reaction | |||
| 317. Willgerodt-Kindler reaction | 433 | (4) | |
| 318. Williamson ether synthesis | 437 | (1) | |
| 319. Wittig reaction | 438 | (1) | |
| 320. [1,2]-Wittig rearrangement | 439 | (1) | |
| 321. [2,3]-Wittig rearrangement | 440 | (1) | |
| 322. Wohl-Ziegler reaction | 441 | (2) | |
| 323. Wolff rearrangement | 443 | (1) | |
| 324. Wolff-Kishner reduction | 444 | (1) | |
| 325. Woodward cis-dihydroxylation | 445 | (1) | |
| 326. Wurtz reaction | 446 | (1) | |
| 327. Yamada coupling reagent | 447 | (1) | |
| 328. Yamaguchi esterification | 448 | (2) | |
| 329. Zaitsev elimination | 450 | (1) | |
| 330. Zincke reaction | 451 | (2) | |
| 331. Zinfin benzidine rearrangement (semidine rearrangement) | 453 | (2) | |
| Subject Index | 455 |
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