Abbreviations |
Abnormal Claisen rearrangement / 1: |
Alder ene reaction / 2: |
Aldol condensation / 3: |
Allan-Robinson reaction / 4: |
Alper carbonylation / 5: |
Amadori rearrangement / 6: |
Angeli-Rimini hydroxamic acid synthesis / 7: |
ANRORC mechanism / 8: |
Arndt-Eistert homologation / 9: |
Auwers reaction / 10: |
Baeyer-Drewson indigo synthesis / 11: |
Baeyer-Villiger oxidation / 12: |
Baker-Venkataraman rearrangement / 13: |
Bamberger rearrangement / 14: |
Bamford-Stevens reaction / 15: |
Bargellini reaction / 16: |
Bartoli indole synthesis / 17: |
Barton decarboxylation / 18: |
Barton-McCombie deoxygenation / 19: |
Barton nitrite photolysis / 20: |
Baylis-Hillman reaction / 21: |
Beckmann rearrangement / 22: |
Beirut reaction / 23: |
Benzilic acid rearrangement / 24: |
Benzoin condensation / 25: |
Bergman cyclization / 26: |
Biginelli pyrimidone synthesis / 27: |
Birch reduction / 28: |
Bischler-Möhlau indole synthesis / 29: |
Bischler-Napieralski reaction / 30: |
Blaise reaction / 31: |
Blanc chloromethylation reaction / 32: |
Boekelheide reaction / 33: |
Boger pyridine synthesis / 34: |
Boord reaction / 35: |
Borsche-Drechsel cyclization / 36: |
Boulton-Katritzky rearrangement / 37: |
Bouveault aldehyde synthesis / 38: |
Bouveault-Blanc reduction / 39: |
Boyland-Sims oxidation / 40: |
Bradsher reaction / 41: |
Brook rearrangement / 42: |
Brown hydroboration reaction / 43: |
Bucherer carbazole synthesis / 44: |
Bucherer reaction / 45: |
Bucherer-Bergs reaction / 46: |
Buchner-Curtius-Schlotterbeck reaction / 47: |
Buchner method of ring expansion / 48: |
Buchwald-Hartwig C-N bond and C-O bond formation reactions / 49: |
Burgess dehydrating reagent / 50: |
Cadiot-Chodkiewicz coupling / 51: |
Cannizzaro dispropotionation reaction / 52: |
Carroll rearrangement / 53: |
Castro-Stephens coupling / 54: |
Chapman rearrangement / 55: |
Chichibabin amination reaction / 56: |
Chichibabin pyridine synthesis / 57: |
Chugaev reaction / 58: |
Ciamician-Dennsted rearrangement / 59: |
Claisen condensation / 60: |
Claisen rearrangement / 61: |
Clarke-Eschweiler reductive alkylation of amines / 62: |
Clemmensen reduction / 63: |
Combes quinoline synthesis / 64: |
Conrad-Limpach reaction / 65: |
Cook-Heilbron thiazole synthesis / 66: |
Cope elimination reaction / 67: |
Cope, oxy-Cope, and anionic oxy-Cope rearrangements / 68: |
Corey-Bakshi-Shibata (CBS) reduction / 69: |
Corey-Chaykovsky reaction / 70: |
Corey-Fuchs reaction / 71: |
Corey-Kim oxidation / 72: |
Corey-Winter olefin synthesis / 73: |
Cornforth rearrangement / 74: |
Criegee glycol cleavage / 75: |
Criegee mechanism of ozonolysis / 76: |
Curtius rearrangement / 77: |
Dakin oxidation / 78: |
Dakin-West reaction / 79: |
Danheiser annulation / 80: |
Darzens glycidic ester condensation / 81: |
Davis chiral oxaziridine reagent / 82: |
de Mayo reaction / 83: |
Demjanov rearrangement / 84: |
Dess-Martin periodinane oxidation / 85: |
Dieckmann condensation / 86: |
Diels-Alder reaction / 87: |
Dienone-phenol rearrangement / 88: |
Di-?-methane rearrangement / 89: |
Doebner reaction / 90: |
Doebner-von Miller reaction / 91: |
Doering-LaFlamme allene synthesis / 92: |
Dornow-Wiehler isoxazole synthesis / 93: |
Dötz reaction / 94: |
Dowd ring expansion / 95: |
Dutt-Wormall reaction / 96: |
Eglinton reaction / 97: |
Eschenmoser coupling reaction / 98: |
Eschenmoser-Tanabe fragmentation / 99: |
Étard reaction / 100: |
Evans aldol reaction / 101: |
Favorskii rearrangement and Quasi-Favorskii rearrangement / 102: |
Feist-Bénary furan synthesis / 103: |
Ferrier rearrangement / 104: |
Finkelstein reaction / 105: |
Fischer-Hepp rearrangement / 106: |
Fischer indole synthesis / 107: |
Fischer-Speier esterification / 108: |
Fleming oxidation / 109: |
Forster reaction / 110: |
Frater-Seebach alkylation / 111: |
Friedel-Crafts reaction / 112: |
Friedländer synthesis / 113: |
Fries rearrangement / 114: |
Fritsch-Buttenberg-Wiechell rearrangement / 115: |
Fujimoto-Belleau reaction / 116: |
Fukuyama amine synthesis / 117: |
Gabriel synthesis / 118: |
Gassman indole synthesis / 119: |
Gattermann-Koch reaction / 120: |
Gewald aminothiophene synthesis / 121: |
Glaser coupling / 122: |
Gomberg-Bachmann reaction / 123: |
Gribble indole reduction / 124: |
Gribble reduction of diaryl ketones / 125: |
Grignard reaction / 126: |
Grob fragmentation / 127: |
Guareschi-Thorpe condensation / 128: |
Hajos-Wiechert reaction / 129: |
Haller-Bauer reaction / 130: |
Hantzsch pyridine synthesis / 131: |
Hantzsch pyrrole synthesis / 132: |
Haworth reaction / 133: |
Hayashi rearrangement / 134: |
Heck reaction / 135: |
Hegedus indole synthesis / 136: |
Hell-Volhardt-Zelinsky reaction / 137: |
Henry reaction (nitroaldol reaction) / 138: |
Herz reaction / 139: |
Heteroaryl Heck reaction / 140: |
Hiyama cross-coupling reaction / 141: |
Hoch-Campbell aziridine synthesis / 142: |
Hodges-Vedejs metallation of oxazoles / 143: |
Hofmann rearrangement (Hofmann degradation reaction) / 144: |
Hofmann-Löffler-Freytag reaction / 145: |
Hofmann-Martius reaction (Reilly-Hickinbottom rearrangement) / 146: |
Hooker oxidation / 147: |
Horner-Wadsworth-Emmons reaction / 148: |
Houben-Hoesch synthesis / 149: |
Hunsdiecker reaction / 150: |
Ing-Manske procedure / 151: |
Jacobsen-Katsuki epoxidation / 152: |
Jacobsen rearrangement / 153: |
Japp-Klingemann hydrazone synthesis / 154: |
Julia-Lythgoe olefination / 155: |
Kahne glycosidation / 156: |
Keck stereoselective allylation / 157: |
Keck macrolactonization / 158: |
Kemp elimination / 159: |
Kennedy oxidative cyclization / 160: |
Kharasch addition reaction / 161: |
Knoevenagel condensation / 162: |
Knorr pyrrole synthesis / 163: |
Koch carbonylation reaction (Koch-Haaf carbonylation reaction) / 164: |
Koenig-Knorr glycosidation / 165: |
Kolbe electrolytic coupling / 166: |
Kolbe-Schmitt reaction / 167: |
Kostanecki reaction / 168: |
Krapcho decarboxylation / 169: |
Kröhnke reaction (pyridine synthesis) / 170: |
Kumada cross-coupling reaction / 171: |
Larock indole synthesis / 172: |
Lawesson's reagent / 173: |
Leuckart-Wallach reaction / 174: |
Lieben haloform reaction / 175: |
Liebeskind-Srogl coupling / 176: |
Lossen rearrangement / 177: |
Luche reduction / 178: |
McFadyen-Stevens reduction / 179: |
McLafferty rearrangement / 180: |
McMurry coupling / 181: |
Madelung indole synthesis / 182: |
Mannich reaction / 183: |
Marshall boronate fragmentation / 184: |
Martin's sulfurane dehydrating reagent / 185: |
Masamune-Roush conditions / 186: |
Meerwein arylation / 187: |
Meerwein-Ponndorf-Verley reduction / 188: |
Meinwald rearrangement / 189: |
Meisenheimer complex / 190: |
Meisenheimer rearrangement / 191: |
Meyer-Schuster rearrangement / 192: |
Michael addition / 193: |
Michaelis-Arbuzov phosphonate synthesis / 194: |
Midland reduction / 195: |
Miller-Loudon-Snyder nitrile synthesis / 196: |
Mislow-Evans rearrangement / 197: |
Mitsunobu reaction / 198: |
Miyaura boration reaction / 199: |
Moffatt oxidation / 200: |
Morgan-Walls reaction (Pictet-Hubert reaction) / 201: |
Mori-Ban indole synthesis / 202: |
Morin rearrangement / 203: |
Mukaiyama aldol reaction / 204: |
Mukaiyama esterification / 205: |
Myers-Saito cyclization / 206: |
Nametkin rearrangement (retropinacol rearrangement) / 207: |
Nazarov cyclization / 208: |
Neber rearrangement / 209: |
Nef reaction / 210: |
Negishi cross-coupling reaction / 211: |
Nenitzescu indole synthesis / 212: |
Nicholas reaction / 213: |
Noyori asymmetric hydrogenation / 214: |
Nozaki-Hiyama-Kishi reaction / 215: |
Oppenauer oxidation / 216: |
Orton rearrangement / 217: |
Overman rearrangement / 218: |
Paal-Knorr furan synthesis / 219: |
Paal-Knorr pyrrole synthesis / 220: |
Parham cyclization / 221: |
Passerini reaction / 222: |
Paterno-Büchi reaction / 223: |
Pauson-Khand cyclopentenone synthesis / 224: |
Payne rearrangement / 225: |
Pechmann condensation (coumarin synthesis) / 226: |
Pechmann pyrazole synthesis / 227: |
Perkin reaction (cinnamic acid synthesis) / 228: |
Perkow vinyl phosphate synthesis / 229: |
Peterson olefination / 230: |
Pfau-Plattner azulene synthesis / 231: |
Pfitzinger quinoline synthesis / 232: |
Pictet-Gams isoquinoline synthesis / 233: |
Pictet-Spengler tetrahydroisoquinoline synthesis / 234: |
Pinacol rearrangement / 235: |
Pinner synthesis / 236: |
Polonovski reaction / 237: |
Polonovski-Potier rearrangement / 238: |
Pomeranz-Fritsch reaction / 239: |
Prévost trans-dihydroxylation / 240: |
Prilezhaev reaction / 241: |
Prins reaction / 242: |
Pschorr ring closure / 243: |
Pummerer rearrangement / 244: |
Ramberg-Bäcklund olefin synthesis / 245: |
Reformatsky reaction / 246: |
Regitz diazo synthesis / 247: |
Reimer-Tiemann reaction / 248: |
Reissert reaction (aldehyde synthesis) / 249: |
Riley oxidation (selenium dioxide oxidation) / 250: |
Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts / 251: |
Ritter reaction / 252: |
Robinson annulation / 253: |
Robinson-Schöpf reaction / 254: |
Rosenmund reduction / 255: |
Roush allylboronate reagent / 256: |
Rubottom oxidation / 257: |
Rupe rearrangement / 258: |
Rychnovsky polyol synthesis / 259: |
Sakurai allylation reaction (Hosomi-Sakurai reaction) / 260: |
Sandmeyer reaction / 261: |
Sarett oxidation / 262: |
Schiemann reaction (Balz-Schiemann reaction) / 263: |
Schlosser modification of the Wittig reaction / 264: |
Schmidt reaction / 265: |
Schmidt's trichloroacetimidate glycosidation reaction / 266: |
Scholl reaction / 267: |
Schöpf reaction / 268: |
Schotten-Baumann reaction / 269: |
Shapiro reaction / 270: |
Sharpless asymmetric amino hydroxylation / 271: |
Sharpless asymmetric epoxidation / 272: |
Sharpless dihydroxylation / 273: |
Shi asymmetric epoxidation / 274: |
Simmons-Smith reaction / 275: |
Simonini reaction / 276: |
Simonis chromone cyclization / 277: |
Skraup quinoline synthesis / 278: |
Smiles rearrangement / 279: |
Sommelet reaction / 280: |
Sommelet-Hauser (ammonium ylide) rearrangement / 281: |
Sonogashira reaction / 282: |
Staudinger reaction / 283: |
Stetter reaction (Michael-Stetter reaction) / 284: |
Stevens rearrangement / 285: |
Stieglitz rearrangement / 286: |
Still-Gennari phosphonate reaction / 287: |
Stille coupling / 288: |
Stille-Kelly reaction / 289: |
Stobbe condensation / 290: |
Stollé synthesis / 291: |
Stork enamine reaction / 292: |
Strecker amino acid synthesis / 293: |
Suzuki coupling / 294: |
Swern oxidation / 295: |
Tamao-Kumada oxidation / 296: |
Tebbe olefination (Petasis alkenylation) / 297: |
Thorpe-Ziegler reaction / 298: |
Tiemann rearrangement / 299: |
Tiffeneau-Demjanov rearrangement / 300: |
Tishchenko reaction / 301: |
Tollens reaction / 302: |
Tsuji-Trost allylation / 303: |
Ueno-Stork cyclization / 304: |
Ugi reaction / 305: |
Ullmann reaction / 306: |
Vilsmeier-Haack reaction / 307: |
von Braun reaction / 308: |
von Richter reaction / 309: |
Wacker oxidation / 310: |
Wagner-Meerwein rearrangement / 311: |
Wallach rearrangement / 312: |
Weinreb amide / 313: |
Weiss reaction / 314: |
Wenker aziridine synthesis / 315: |
Wharton oxygen transposition reaction / 316: |
Willgerodt-Kindler reaction / 317: |
Williamson ether synthesis / 318: |
Wittig reaction / 319: |
[1,2]-Wittig rearrangement / 320: |
[2,3]-Wittig rearrangement / 321: |
Wohl-Ziegler reaction / 322: |
Wolff rearrangement / 323: |
Wolff-Kishner reduction / 324: |
Woodward cis-dihydroxylation / 325: |
Wurtz reaction / 326: |
Yamada coupling reagent / 327: |
Yamaguchi esterification / 328: |
Zaitsev elimination / 329: |
Zincke reaction / 330: |
Zinin benzidine rearrangement (semidine rearrangement) / 331: |
Subject Index |