Alder ene reaction 1
Aldol condensation 3
Algar-Flynn-Oyamada reaction 5
Allan-Robinson reaction 8
Appel reaction 10
Arndt-Eistert homologation 12
Baeyer-Villiger oxidation 14
Baker-Venkataraman rearrangement 16
Bamberger rearrangement 18
Bamford-Stevens reaction 20
Barbier coupling reaction 22
Bargellini reaction 24
Bartoli indole synthesis 26
Barton radical decarboxylation 28
Barton-McCombie deoxygenation 30
Barton nitrite photolysis 32
Barton-Zard reaction 34
Batcho-Leimgruber indole synthesis 36
Baylis-Hillman reaction 39
Beckmann rearrangement 41
Beirut reaction 43
Benzilic acid rearrangement 45
Benzoin condensation 47
Bergman cyclization 49
Biginelli pyrimidone synthesis 51
Birch reduction 53
Bischler-M？hlau indole synthesis 55
Bischler-Napieralski reaction 57
Blaise reaction 59
Blanc chloromethylation 61
Blum aziridine synthesis 63
Boekelheide reaction 65
Boger pyridine synthesis 67
Borch reductive amination 69
Borsche-Drechsel cyclization 71
Boulton-Katritzky rearrangement 73
Bouveault aldehyde synthesis 75
Bouveault-Blanc reduction 77
Boyland-Sims oxidation 79
Bradsher reaction 81
Brook rearrangement 83
Brown hydroboration 85
Bucherer carbazole synthesis 87
Bucherer reaction 90
Bucherer-Bergs reaction 92
Büchner-Curtius-Schlotterbeck reaction 94
Büchner method of ring expansion 96
Buchwald-Hartwig C-N bond and C-O bond formation reactions 98
Burgess dehydrating reagent 100
Cadiot-Chodkiewicz coupling 102
Camps quinolinol synthesis 104
Cannizzaro dispropotionation 107
Carroll rearrangement 109
Castro-Stephens coupling 112
Chan alkyne reduction 114
Chan-Lam coupling reaction 116
Chapman rearrangement 118
Chichibabin pyridine synthesis 120
Chugaev reaction 123
Ciamician-Dennsted rearrangement 125
Claisen condensation 127
Claisen isoxazole synthesis 129
Claisen rearrangement 131
Abnormal Claisen rearrangement 133
Eschenmoser-Claisen amide acetal rearrangement 135
Ireland-Claisen(silyl ketene acetal)rearrangement 137
Johnson-Claisen(orthoester)rearrangement 139
Clemmensen reduction 141
Combes quinoline synthesis 144
Conrad-Limpach reaction 147
Cope elimination reaction 149
Cope rearrangement 151
Oxy-Cope rearrangement 152
Anionic oxy-Cope rearrangement 153
Corey-Bakshi-Shibata(CBS)reduction 154
Corey-Chaykovsky reaction 157
Corey-Fuchs reaction 160
Corey-Kim oxidation 162
Corey-Nicolaou macrolactonization 164
Corey-Seebach dithiane reaction 166
Corey-Winter olefin synthesis 168
Cfiegee glycol cleavage 171
Criegee mechanism of ozonolysis 173
Curtius rearrangement 175
Dakin oxidation 177
Dakin-West reaction 179
Danheiser annulation 181
Darzens glycidic ester condensation 183
Davis chiral oxaziridine reagent 185
Delépine amine synthesis 187
de Mayo reaction 189
Demjanov rearrangement 191
Tiffeneau-Demjanov rearrangement 193
Dess-Martin oxidation 195
Dieckmann condensation 197
Diels-Alder reaction 199
Dienone-phenol rearrangement 202
Di-π-methane rearrangement 204
Doebner quinoline synthesis 206
D？tz reaction 208
Dowd-Beckwith ring expansion 210
Erlenmeyer-Pl？chl azlactone synthesis 212
Eschenmoser-Tanabe fragmentation 214
Eschweiler-Clarke reductive alkylation of amines 216
Evans aldol reaction 218
Favorskii rearrangement and quasi-Favorskii rearrangement 220
Feist-Bénary furan synthesis 222
Ferrier carbocyclization 224
Ferrier glycal allylic rearrangement 227
Fiesselmann thiophene synthesis 230
Fischer indole synthesis 233
Fischer oxazole synthesis 235
Fleming-Tamao oxidation 237
Tamao-Kumada oxidation 239
Friedel-Crafts reaction 240
Ffiedl？nder quinoline synthesis 243
Fries rearrangement 245
Fukuyama amine synthesis 247
Fukuyama reduction 249
Gabriel synthesis 251
Ing-Manske procedure 253
Gabriel-Colman rearrangement 255
Gassman indole synthesis 257
Gattermann-Koch reaction 259
Gewald aminothiophene synthesis 261
Glaser coupling 263
Eglinton coupling 265
Gomberg-Bachmann reaction 267
Gould-Jacobs reaction 269
Grignard reaction 271
Grob fragmentation 273
Guareschi-Thorpe condensation 275
Hajos-Wiechert reaction 277
Haller-Bauer reaction 279
Hantzsch dihydropyridine synthesis 281
Hantzsch pyrrole synthesis 283
Heck reaction 285
Heteroaryl Heck reaction 287
Hegedus indole synthesis 289
Hell-Volhard-Zelinsky reaction 291
Henry nitroaldol reaction 293
Hinsberg synthesis of thiophene deritvatives 295
Hiyama cross-coupling reaction 297
Hiyama-Denmark cross-coupling reaction 299
Hofmann rearrangement 302
Hofmann-L？ffler-Freytag reaction 304
Horner-Wadsworth-Emmons reaction 306
Houben-Hoesch synthesis 308
Hunsdiecker-Borodin reaction 310
Hurd-Mori 1,2,3-thiadiazole synthesis 312
Jacobsen-Katsuki epoxidation 314
Japp-Klingemann hydrazone synthesis 316
Jones oxidation 318
Julia-Kocienski olefination 321
Julia-Lythgoe olefination 323
Kahne-Crich glycosidation 325
Keck macrolactonization 327
Knoevenagel condensation 329
Knorr pyrazole synthesis 331
Paal-Knorr pyrrole synthesis 333
Koch-Haaf carbonylation 335
Koenig-Knorr glycosidation 337
Kolbe-Schmitt reaction 339
Kostanecki reaction 341
Kr？hnke pyridine synthesis 343
Kumada cross-coupling reaction 345
Lawesson's reagent 348
Leuckart-Wallach reaction 350
Lossen rearrangement 352
McFadyen-Stevens reduction 354
McMurry coupling 356
MacMillan catalyst 358
Mannich reaction 361
Marshall boronate fragmentation 363
Martin's sulfurane dehydrating reagent 365
Masamune-Roush conditions 367
Meerwein-Ponndorf-Verley reduction 369
Meisenheimer complex 371
[1,2]-Meisenheimer rearrangement 372
[2,3]-Meisenheimer rearrangement 374
Meth-Cohn quinoline synthesis 376
Meyers oxazoline method 378
Meyer-Schuster rearrangement 380
Michael addition 382
Michaelis-Arbuzov phosphonate synthesis 384
Midland reduction 386
Mislow-Evans rearrangement 388
Mitsunobu reaction 390
Miyaura borylation 392
Moffatt oxidation 394
Montgomery coupling 396
Morgan-Walls reaction 399
Pictet-Hubert reaction 400
Mori-Ban indole synthesis 401
Mukaiyama aldol reaction 403
Mukaiyama Michael addition 405
Mukaiyama reagent 406
Myers-Saito cyclization 408
Nazarov cyclization 410
Neber rearrangement 412
Nef reaction 414
Negishi cross-coupling reaction 416
Nenitzescu indole synthesis 418
Nicholas reaction 420
Nicolaou dehydrogenation 422
Nicolaou hydroxy-dithioketal cyclization 424
Nicolaou hydroxy-ketone reductive cyclic ether formation 426
Nicolaou oxyselenation 428
Noyori asymmetric hydrogenation 430
Nozaki-Hiyama-Kishi reaction 432
Oppenauer oxidation 434
Overman rearrangement 436
Paal thiophene synthesis 438
Paal-Knorr furan synthesis 440
Parham cyclization 442
Passerini reaction 444
Paternó-Büichi reaction 446
Pauson-Khand cyclopentenone synthesis 448
Payne rearrangement 450
Pechmann coumarin synthesis 452
Perkin reaction 454
Petasis reaction 456
Peterson olefination 458
Pictet-Gams isoquinoline synthesis 460
Pictet-Spengler tetrahydroisoquinoline synthesis 462
Pinacol rearrangement 464
Pinner reaction 466
Polonovski reaction 468
Polonovski-Potier rearrangement 470
Pomeranz-Fritsch reaction 472
Schlitter-Müller modification 473
Prévost trans-dihydroxylation 475
Woodward cis-dihydroxylation 476
Prins reaction 478
Pschorr cyclization 480
Pummerer rearrangement 483
Ramberg-B？cklund reaction 485
Reformatsky reaction 487
Regitz diazo synthesis 489
Reimer-Tiemann reaction 492
Reissert aldehyde synthesis 494
Reissert indole synthesis 497
Ring-closing metathesis 499
Ritter reaction 501
Robinson annulation 503
Robinson-Gabriel synthesis 505
Robinson-Sch？pf reaction 507
Rosenmund reduction 509
Rubottom oxidation 511
Rupe rearrangement 513
Saegusa oxidation 515
Sakurai allylation reaction 518
Sandmeyer reaction 520
Schiemann reaction 522
Schmidt reaction 524
Schmidt's trichloroacetimidate glycosidation reaction 526
Shapiro reaction 529
Sharpless asymmetric amino hydroxylation 531
Sharpless asymmetric epoxidation 533
Sharpless asymmetric dihydroxylation 536
Sharpless olefin synthesis 540
Simmons-Smith reaction 543
Skraup quinoline synthesis 545
Doebner-von Miller reaction 547
Smiles rearrangement 549
Newman-Kwart reaction 551
Truce-Smile rearrangement 553
Sommelet reaction 555
Sommelet-Hauser rearrangement 557
Sonogashira reaction 559
Staudinger ketene cycloaddition 561
Staudinger reduction 563
Sternbach benzodiazepine synthesis 565
Stetter reaction 567
Still-Gennari phosphonate reaction 569
Stille coupling 571
Stille-Kelly reaction 573
Stobbe condensation 575
Stork enamine reaction 577
Strecker amino acid synthesis 579
Suzuki coupling 581
Swern oxidation 583
Takai iodoalkene synthesis 585
Tebbe olefination 587
Petasis alkenylation 587
TEMPO-mediated oxidation 589
Thorpe-Ziegler reaction 592
Tsuji-Trost allylation 594
Ugi reaction 596
Ullmann reaction 599
van Leusen oxazole synthesis 601
Vilsmeier-Haack reaction 603
Vilsmeier mechanism for acid chloride formation 605
Vinylcyclopropane-cyclopentene rearrangement 606
von Braun reaction 608
Wacker oxidation 610
Wagner-Meerwein rearrangement 612
Weiss-Cook reaction 614
Wharton oxygen transposition reaction 616
Willgerodt-Kindler reaction 618
Wittig reaction 621
Schlosser modification of the Wittig reaction 622
[l,2]-Wittig rearrangement 624
[2,3]-Wittig rearrangement 626
Wohl-Ziegler reaction 628
Wolff rearrangement 630
Wolff-Kishner reduction 632
Yamaguchi esterification 634
Zincke reaction 637
Subject Index 641