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Author(s):
Jie Jack Li
Publication date
(Print):
2003
Publisher:
Springer Berlin Heidelberg
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Book
ISBN (Print):
978-3-662-05338-6
ISBN (Electronic):
978-3-662-05336-2
Publication date (Print):
2003
DOI:
10.1007/978-3-662-05336-2
SO-VID:
62d71b1b-7115-4378-aaf2-335428e9fbfd
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http://www.springer.com/tdm
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Book chapters
pp. 1
Abnormal Claisen rearrangement
pp. 2
Alder ene reaction
pp. 3
Aldol condensation
pp. 4
Allan-Robinson reaction
pp. 6
Alper carbonylation
pp. 8
Amadori rearrangement
pp. 9
Angeli-Rimini hydroxamic acid synthesis
pp. 10
ANRORC mechanism
pp. 11
Arndt-Eistert homologation
pp. 13
Auwers reaction
pp. 14
Baeyer-Drewson indigo synthesis
pp. 16
Baeyer-Villiger oxidation
pp. 17
Baker-Venkataraman rearrangement
pp. 18
Bamberger rearrangement
pp. 19
Bamford-Stevens reaction
pp. 20
Bargellini reaction
pp. 21
Bartoli indole synthesis
pp. 22
Barton decarboxylation
pp. 23
Barton-McCombie deoxygenation
pp. 24
Barton nitrite photolysis
pp. 26
Baylis-Hillman reaction
pp. 28
Beckmann rearrangement
pp. 29
Beirut reaction
pp. 31
Benzilic acid rearrangement
pp. 32
Benzoin condensation
pp. 33
Bergman cyclization
pp. 34
Biginelli pyrimidone synthesis
pp. 36
Birch reduction
pp. 38
Bischler-Möhlau indole synthesis
pp. 39
Bischler-Napieralski reaction
pp. 40
Blaise reaction
pp. 41
Blanc chloromethylation reaction
pp. 42
Boekelheide reaction
pp. 43
Boger pyridine synthesis
pp. 44
Boord reaction
pp. 45
Borsche-Drechsel cyclization
pp. 46
Boulton-Katritzky rearrangement
pp. 47
Bouveault aldehyde synthesis
pp. 48
Bouveault-Blanc reduction
pp. 49
Boyland-Sims oxidation
pp. 51
Bradsher reaction
pp. 52
Brook rearrangement
pp. 53
Brown hydroboration reaction
pp. 54
Bucherer carbazole synthesis
pp. 56
Bucherer reaction
pp. 57
Bucherer-Bergs reaction
pp. 58
Buchner-Curtius-Schlotterbeck reaction
pp. 59
Buchner method of ring expansion
pp. 60
Buchwald-Hartwig C-N bond and C-O bond formation reactions
pp. 61
Burgess dehydrating reagent
pp. 62
Cadiot-Chodkiewicz coupling
pp. 63
Cannizzaro disproportionation reaction
pp. 65
Carroll rearrangement
pp. 66
Castro-Stephens coupling
pp. 67
Chapman rearrangement
pp. 68
Chichibabin amination reaction
pp. 69
Chichibabin pyridine synthesis
pp. 71
Chugaev elimination
pp. 72
Ciamician-Dennsted rearrangement
pp. 73
Claisen condensation
pp. 74
Claisen, Eschenmoser-Claisen, Johnson-Claisen, and Ireland-Claisen rearrangements
pp. 76
Clarke-Eschweiler reductive alkylation of amines
pp. 77
Clemmensen reduction
pp. 79
Combes quinoline synthesis
pp. 81
Conrad-Limpach reaction
pp. 82
Cook-Heilbron thiazole synthesis
pp. 83
Cope elimination reaction
pp. 84
Cope, oxy-Cope, and anionic oxy-Cope rearrangements
pp. 86
Corey-Bakshi-Shibata (CBS) reduction
pp. 88
Corey-Chaykovsky reaction
pp. 90
Corey-Fuchs reaction
pp. 92
Corey-Kim oxidation
pp. 93
Corey-Winter olefin synthesis
pp. 95
Cornforth rearrangement
pp. 96
Criegee glycol cleavage
pp. 97
Criegee mechanism of ozonolysis
pp. 98
Curtius rearrangement
pp. 99
Dakin oxidation
pp. 100
Dakin-West reaction
pp. 102
Danheiser annulation
pp. 103
Darzens glycidic ester condensation
pp. 104
Davis chiral oxaziridine reagents
pp. 105
De Mayo reaction
pp. 107
Demjanov rearrangement
pp. 109
Dess-martin periodinane oxidation
pp. 110
Dieckmann condensation
pp. 111
Diels-Alder reaction
pp. 113
Dienone-phenol rearrangement
pp. 114
Di-π-methane rearrangement
pp. 115
Doebner reaction
pp. 117
Doebner–von Miller reaction
pp. 119
Doering–LaFlamme allene synthesis
pp. 120
Dornow–Wiehler isoxazole synthesis
pp. 122
Dötz reaction
pp. 123
Dowd ring expansion
pp. 125
Dutt-wormall reaction
pp. 126
Eglinton reaction
pp. 127
Eschenmoser coupling reaction
pp. 128
Eschenmoser-Tanabe fragmentation
pp. 129
Étard reaction
pp. 130
Evans aldol reaction
pp. 132
Favorskii rearrangement and Quasi-Favorskii rearrangement
pp. 134
Feist-Bénary furan synthesis
pp. 135
Ferrier rearrangement
pp. 136
Finkelstein reaction
pp. 137
Fischer-Hepp rearrangement
pp. 138
Fischer indole synthesis
pp. 139
Fischer-Speier esterification
pp. 140
Fleming oxidation
pp. 142
Forster reaction
pp. 144
Frater-Seebach alkylation
pp. 145
Friedel-Crafts reaction
pp. 147
Friedländer synthesis
pp. 149
Fries rearrangement
pp. 151
Fritsch-Buttenberg-Wiechell rearrangement
pp. 152
Fujimoto-Belleau reaction
pp. 153
Fukuyama amine synthesis
pp. 155
Gabriel synthesis
pp. 156
Gassman indole synthesis
pp. 157
Gattermann-Koch reaction
pp. 158
Gewald aminothiophene synthesis
pp. 160
Glaser coupling
pp. 161
Gomberg-Bachmann reaction
pp. 162
Gribble indole reduction
pp. 163
Gribble reduction of diaryl ketones
pp. 164
Grignard reaction
pp. 166
Grob fragmentation
pp. 168
Guareschi-Thorpe condensation
pp. 169
Hajos-Wiechert reaction
pp. 171
Haller-Bauer reaction
pp. 172
Hantzsch pyridine synthesis
pp. 174
Hantzsch pyrrole synthesis
pp. 175
Haworth reaction
pp. 177
Hayashi rearrangement
pp. 179
Heck reaction
pp. 181
Hegedus indole synthesis
pp. 182
Hell-Volhardt-Zelinsky reaction
pp. 183
Henry reaction (nitroaldol reaction)
pp. 184
Herz reaction
pp. 186
Heteroaryl Heck reaction
pp. 187
Hiyama cross-coupling reaction
pp. 189
Hoch-Campbell aziridine synthesis
pp. 191
Hodges-Vedejs metallation of oxazoles
pp. 192
Hofmann rearrangement (Hofmann degradation reaction)
pp. 193
Hofmann-Löffler-Freytag reaction
pp. 194
Hofmann-Martius reaction
pp. 196
Hooker oxidation
pp. 198
Horner-Wadsworth-Emmons reaction
pp. 200
Houben-Hoesch reaction
pp. 202
Hunsdiecker reaction
pp. 203
Ing-Manske procedure
pp. 204
Jacobsen-Katsuki epoxidation
pp. 206
Jacobsen rearrangement
pp. 208
Japp-Klingemann hydrazone synthesis
pp. 209
Julia-Lythgoe olefination
pp. 211
Kahne glycosidation
pp. 213
Keck stereoselective allylation
pp. 215
Keck macrolactonization
pp. 217
Kemp elimination
pp. 218
Kennedy oxidative cyclization
pp. 219
Kharasch addition reaction
pp. 220
Knöevenagel condensation
pp. 222
Knorr pyrrole synthesis
pp. 223
Koch carbonylation reaction (Koch-Haaf carbonylation reaction)
pp. 225
Koenig-Knorr glycosidation
pp. 226
Kolbe electrolytic coupling
pp. 227
Kolbe-Schmitt reaction
pp. 228
Kostanecki reaction
pp. 230
Krapcho decarboxylation
pp. 231
Kröhnke reaction (pyridine synthesis)
pp. 233
Kumada cross-coupling reaction
pp. 235
Larock indole synthesis
pp. 236
Lawesson’s reagent
pp. 237
Leuckart-Wallach reaction
pp. 238
Lieben haloform reaction
pp. 239
Liebeskind-Srogl coupling
pp. 240
Lossen rearrangement
pp. 241
Luche reduction
pp. 242
McFadyen-Stevens reduction
pp. 243
McLafferty fragmentation
pp. 244
McMurry coupling
pp. 245
Madelung indole synthesis
pp. 246
Mannich reaction
pp. 248
Marshall boronate fragmentation
pp. 249
Martin’s sulfurane dehydrating reagent
pp. 251
Masamune-Roush conditions
pp. 253
Meerwein arylation
pp. 254
Meerwein-Ponndorf-Verley reduction
pp. 255
Meinwald rearrangement
pp. 256
Meisenheimer complex
pp. 258
Meisenheimer rearrangement
pp. 259
Meyer-Schuster rearrangement
pp. 260
Michael addition
pp. 261
Michaelis-Arbuzov phosphonate synthesis
pp. 262
Midland reduction
pp. 263
Miller-Loudon-Snyder nitrile synthesis
pp. 264
Mislow-Evans rearrangement
pp. 265
Mitsunobu reaction
pp. 266
Miyaura boration reaction
pp. 267
Moffatt oxidation
pp. 269
Morgan-Walls reaction (Pictet-Hubert reaction)
pp. 270
Mori-Ban indole synthesis
pp. 272
Morin rearrangement
pp. 274
Mukaiyama aldol reaction
pp. 275
Mukaiyama esterification
pp. 277
Myers-Saito cyclization
pp. 279
Nametkin rearrangement (Retropinacol rearrangement)
pp. 280
Nazarov cyclization
pp. 281
Neber rearrangement
pp. 282
Nef reaction
pp. 283
Negishi cross-coupling reaction
pp. 284
Nenitzescu indole synthesis
pp. 286
Nicholas reaction
pp. 287
Noyori asymmetric hydrogenation
pp. 289
Nozaki-Hiyama-Kishi reaction
pp. 290
Oppenauer oxidation
pp. 291
Orton rearrangement
pp. 293
Overman rearrangement
pp. 294
Paal-Knorr furan synthesis
pp. 295
Paal-Knorr pyrrole synthesis
pp. 296
Parham cyclization
pp. 298
Passerini reaction
pp. 299
Paterno-Büchi reaction
pp. 300
Pauson-Khand cyclopentenone synthesis
pp. 302
Payne rearrangement
pp. 303
Pechmann condensation (coumarin synthesis)
pp. 304
Pechmann pyrazole synthesis
pp. 305
Perkin reaction (cinnamic acid synthesis)
pp. 307
Perkow vinyl phosphate synthesis
pp. 308
Peterson olefination
pp. 310
Pfau-Plattner azulene synthesis
pp. 311
Pfitzinger quinoline synthesis
pp. 312
Pictet-Gams isoquinoline synthesis
pp. 314
Pictet-Spengler tetrahydroisoquinoline synthesis
pp. 315
Pinacol rearrangement
pp. 316
Pinner synthesis
pp. 317
Polonovski reaction
pp. 319
Polonovski-Potier reaction
pp. 320
Pomeranz-Fritsch reaction
pp. 322
Prévost trans-dihydroxylation
pp. 323
Prilezhaev reaction
pp. 324
Prins reaction
pp. 325
Pschorr ring closure
pp. 327
Pummerer rearrangement
pp. 328
Ramberg—Bäcklund olefin synthesis
pp. 329
Reformatsky reaction
pp. 330
Regitz diazo synthesis
pp. 332
Reimer-Tiemann reaction
pp. 334
Reissert reaction (aldehyde synthesis)
pp. 336
Riley oxidation (selenium dioxide oxidation)
pp. 337
Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts
pp. 339
Ritter reaction
pp. 340
Robinson annulation
pp. 341
Robinson-Schöpf reaction
pp. 343
Rosenmund reduction
pp. 344
Roush allylboronate reagent
pp. 345
Rubottom oxidation
pp. 346
Rupe rearrangement
pp. 347
Rychnovsky polyol synthesis
pp. 349
Sakurai allylation reaction (Hosomi-Sakurai reaction)
pp. 351
Sandmeyer reaction
pp. 352
Sarett oxidation
pp. 354
Schiemann reaction (Balz-Schiemann reaction)
pp. 355
Schlosser modification of the Wittig reaction
pp. 356
Schmidt reaction
pp. 357
Schmidt’s trichloroacetimidate glycosidation reaction
pp. 359
Scholl reaction
pp. 361
Schöpf reaction
pp. 362
Schotten-Baumann reaction
pp. 363
Shapiro reaction
pp. 364
Sharpless asymmetric amino hydroxylation
pp. 366
Sharpless asymmetric epoxidation
pp. 369
Sharpless dihydroxylation
pp. 372
Shi asymmetric epoxidation
pp. 374
Simmons-Smith reaction
pp. 375
Simonini reaction
pp. 376
Simonis chromone cyclization
pp. 378
Skraup quinoline synthesis
pp. 380
Smiles rearrangement
pp. 381
Sommelet reaction
pp. 383
Sommelet-Hauser (ammonium ylide) rearrangement
pp. 384
Sonogashira reaction
pp. 386
Staudinger reaction
pp. 387
Stetter reaction (Michael-Stetter reaction)
pp. 389
Stevens rearrangement
pp. 391
Stieglitz rearrangement
pp. 392
Still-gennari phosphonate reaction
pp. 393
Stille coupling
pp. 394
Stille-kelly reaction
pp. 396
Stobbe condensation
pp. 397
Stollé synthesis
pp. 398
Stork enamine reaction
pp. 399
Strecker amino acid synthesis
pp. 401
Suzuki coupling
pp. 402
Swern oxidation
pp. 404
Tamao-Kumada oxidation
pp. 405
Tebbe olefination (Petasis alkenylation)
pp. 407
Thorpe-Ziegler reaction
pp. 408
Tiemann rearrangement
pp. 409
Tiffeneau-Demjanov Rearrangement
pp. 411
Tishchenko reaction
pp. 412
Tollens reaction
pp. 414
Tsuji-Trost reaction
pp. 415
Ueno-Stork cyclization
pp. 416
Ugi reaction
pp. 418
Ullmann reaction
pp. 419
Vilsmeier—Haack reaction
pp. 421
von Braun reaction
pp. 422
Von Richter reaction
pp. 424
Wacker oxidation
pp. 426
Wagner-Meerwein rearrangement
pp. 427
Wallach rearrangement
pp. 428
Weinreb amide
pp. 429
Weiss reaction
pp. 431
Wenker aziridine synthesis
pp. 432
Wharton oxygen transposition reaction
pp. 433
Willgerodt-Kindler reaction
pp. 437
Williamson ether synthesis
pp. 438
Wittig reaction
pp. 439
[1,2]-Wittig rearrangement
pp. 440
[2,3]-Wittig rearrangement
pp. 441
Wohl-Ziegler reaction
pp. 443
Wolff rearrangement
pp. 444
Wolff-Kishner reduction
pp. 445
Woodward cis-dihydroxylation
pp. 446
Wurtz reaction
pp. 447
Yamada coupling reagent
pp. 448
Yamaguchi esterification
pp. 450
Zaitsev elimination
pp. 451
Zincke reaction
pp. 453
Zinin benzidine rearrangement (semidine rearrangement)
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