Preface |
Acknowledgments |
Autobiography |
Chemical Abbreviations |
Abnormal Claisen Rearrangement / Part 1: |
Acetoacetic Ester Condensation / 2: |
Acetoacetic Ester Synthesis / 3: |
Acyloin Condensation / 4: |
Acyloin Rearrangement / 5: |
Adkins Catalyst / 6: |
Ainley and King Synthesis / 7: |
Akabori Amino Acid Reaction / 8: |
Albright-Goldman Oxidation / 9: |
Alder Ene Reaction / 10: |
Alder-Rickert Reaction / 11: |
Aldol Reaction and Aldol Condensation / 12: |
Algar-Flynn-Oyamada (AFO) Reaction / 13: |
Alkene Metathesis / 14: |
Allan-Robinson Condensation / 15: |
Allylic Rearrangement / 16: |
Amadori Rearrangement / 17: |
Andrussow Process / 18: |
Angeli-Remini Reaction / 19: |
ANRORC Rearrangement / 20: |
Anschutz Anthracene Synthesis / 21: |
Appel Reaction / 22: |
Arens-Van Dorp Reaction / 23: |
Arndt-Eistert Synthesis / 24: |
Asinger Reaction / 25: |
Aston-Greenburg Rearrangement / 26: |
Atherton-Todd Reaction / 27: |
Auwers-Skita Rule / 28: |
Aza-Claisen Rearrangement / 29: |
Baddeley Isomerization / 30: |
Baeyer Diarylmethane Synthesis / 31: |
Baeyer-Drewson Reaction / 32: |
Baeyer Indole Synthesis / 33: |
Baeyer Oxindole Synthesis / 34: |
Baeyer Pyridine Synthesis / 35: |
Baeyer-Villiger Oxidation / 36: |
Bailey Peptide Synthesis / 37: |
Bakelite Process / 38: |
Baker-Ollis Sydnones Synthesis / 39: |
Baker-Venkataraman Rearrangement / 40: |
Ball-Goodwin-Morton Oxidation / 41: |
Bally-Scholl Reaction / 42: |
Balsohn Alkylation / 43: |
Balz-Schiemann Reaction / 44: |
Bamberger Rearrangement / 45: |
Bamford-Stevens Reaction / 46: |
Barbier Reaction / 47: |
Barbier-Wieland Degradation / 48: |
Bardhan Sengupta Synthesis / 49: |
Bargellini Condensation / 50: |
Bart Reaction / 51: |
Bartoli Indole Synthesis / 52: |
Barton Decarboxylation / 53: |
Barton Deoxygenation / 54: |
Barton Reaction / 55: |
Barton-Kellogg Olefination / 56: |
Barton-Zard Pyrrole Synthesis / 57: |
Batcho-Leimgruber Indole Synthesis / 58: |
Baudisch Reaction / 59: |
Baumann-Fromm Thiophene Synthesis / 60: |
Baumgarten ?-Amino Ketone Synthesis / 61: |
Baylis-Hillman Reaction / 62: |
B´echamp Reduction / 63: |
Beckmann Rearrangement and Beckmann Fragmentation / 64: |
Bedoukian Halogenation / 65: |
B´ehal-Sommelet Rearrangement / 66: |
Beirut Reaction / 67: |
Bellus-Claisen Rearrangement / 68: |
B´enary Reaction / 69: |
Benkeser Reduction / 70: |
Benzidine Rearrangement / 71: |
Benzilic Acid Rearrangement / 72: |
Benzoin Condensation / 73: |
Bergius Process / 74: |
Bergman Cyclization / 75: |
Bergmann Degradation / 76: |
Bergmann-Stern Azlactone Synthesis / 77: |
Bergmann-Zervas Peptide Synthesis / 78: |
Bernthsen Reaction / 79: |
Berti Olefination / 80: |
Bertram-Walbaum Reaction / 81: |
Betti Reaction / 82: |
Biginelli Reaction / 83: |
Birch Reduction / 84: |
Birckenbach-Goubeau Halogenation / 85: |
Birnbaum-Simonini Reaction / 86: |
Bischler Reaction / 87: |
Bischler-Napieralski Isoquinoline Synthesis / 88: |
Black Rearrangement / 89: |
Blaise Ketone Synthesis / 90: |
Blaise Reaction / 91: |
Blanc Chloromethylation / 92: |
Blanc Rule / 93: |
Blomquist Cyclic Ketone Synthesis / 94: |
Bobbitt Reaction / 95: |
Bodroux Amide Synthesis / 96: |
Bodroux-Chichibabin Reaction / 97: |
B¿oeseken Oxidation / 98: |
Bogert-Cook Synthesis / 99: |
Bohn-Schmidt Reaction / 100: |
Boord Olefin Synthesis / 101: |
Borsche-Berkhout Reaction / 102: |
Borsche-Drechsel Reaction / 103: |
Borsche-Koelsch Cinnoline Synthesis / 104: |
Bougault Reaction / 105: |
Boulton-Katritzky Rearrangement / 106: |
Bourgel Alkyne Synthesis / 107: |
Bouveault Aldehyde Synthesis / 108: |
Bouveault-Blanc Reduction / 109: |
Boyland-Sims Oxidation / 110: |
Bradsher Cyclization / 111: |
Bradsher Cycloaddition / 112: |
Bradsher Pyridinium Salt Synthesis / 113: |
Brandi-Guarna Reaction / 114: |
Breckpot ?-Lactam Synthesis / 115: |
Bredt's Rule / 116: |
Brook Rearrangement / 117: |
Brown Hydroboration / 118: |
Bruckner Isoquinoline Synthesis / 119: |
Bucherer Carbazole Synthesis / 120: |
Bucherer Reaction / 121: |
Bucherer-Bergs Hydantoin Synthesis / 122: |
B¿uchner Ring Expansion / 123: |
B¿uchner-Curtius-Schlotterbeck Reaction / 124: |
Buchwald Indoline Synthesis / 125: |
Buchwald-Hartwig Amination / 126: |
Burton Trifluoromethylation / 127: |
Cadogan-Sundberg Indole Synthesis / 128: |
Caglioti Reaction / 129: |
Cahours-Hofmann Reaction / 130: |
Camps Reaction / 131: |
Cannizzaro Reaction / 132: |
Carboni-Lindsey Reaction / 133: |
Carroll Rearrangement / 134: |
Castro Indole Synthesis / 135: |
Castro-Stephens Coupling / 136: |
Chan Rearrangement / 137: |
Chapman Rearrangement / 138: |
Chichibabin Amination / 139: |
Chichibabin Pyridine Synthesis / 140: |
Chretien-Longi Reaction / 141: |
Chugaev Reaction / 142: |
Ciamician-Dennstedt Reaction / 143: |
Claisen Rearrangement / 144: |
Claisen-Schmidt Condensation / 145: |
Clauson-Kaas Reaction / 146: |
Clay-Kinnear-Perren Condensation / 147: |
Clayton-Jensen Chlorophosphonation / 148: |
Clemmensen Reduction / 149: |
Cohen Reductive Lithiation / 150: |
Combes Quinoline Synthesis / 151: |
Conrad-Limpach Quinoline Synthesis / 152: |
Cope Elimination / 153: |
Cope Rearrangement / 154: |
Corey-Bakshi-Shibata Reduction / 155: |
Corey-Chaykovsky Epoxidation / 156: |
Corey-Fuchs Reaction / 157: |
Corey-Gilman-Ganem Oxidation / 158: |
Corey-Kim Oxidation / 159: |
Corey-Kwiatkowski Reaction / 160: |
Corey-Link Reaction / 161: |
Corey-Schmidt Oxidation / 162: |
Corey-Suggs Oxidation / 163: |
Corey-Winter Olefination / 164: |
Cornforth Rearrangement / 165: |
Craig 2-Bromo-Pyridine Synthesis / 166: |
Cram's Rule / 167: |
Criegee Glycol Oxidation / 168: |
Criegee Ozonolysis / 169: |
Criegee Rearrangement / 170: |
Crum-Brown-Gibson Substitution Rule / 171: |
Curtius Rearrangement / 172: |
[m+n(+. . . )] Cycloaddition / 173: |
[2+2] Cycloaddition / 174: |
Dakin Reaction / 175: |
Dakin-West Reaction / 176: |
Danheiser Annulation / 177: |
Darzens Condensation / 178: |
Darzens Halogenation / 179: |
Darzens Olefin Acylation / 180: |
Darzens-Nenitzescu Reaction / 181: |
Davidson Oxazole Cyclization / 182: |
de Mayo Reaction / 183: |
Decker-Becker Secondary Amine Synthesis / 184: |
Del´epine Reaction / 185: |
Demjanov Rearrangement / 186: |
Dess-Martin Periodinane Oxidation / 187: |
D-Homo Rearrangement / 188: |
Dieckmann Condensation / 189: |
Diels-Alder Reaction / 190: |
Diels-Reese Reaction / 191: |
Dienol-Benzene Rearrangement / 192: |
Dienone-Phenol Rearrangement / 193: |
Dimroth Rearrangement / 194: |
Di-Π-Methane Rearrangement / 195: |
1,3-Dipolar Cycloaddition / 196: |
Doebner Reaction / 197: |
Doebner-Miller Reaction / 198: |
Doering-Moore-Skattebøl Reaction / 199: |
Dotz Benzannulation / 200: |
Dowd-Beckwith Ring Expansion / 201: |
Duff Reaction / 202: |
Dutt-Wormall Reaction / 203: |
Eastwood Olefination / 204: |
Eder Reaction / 205: |
Edman Degradation / 206: |
Eglinton Coupling / 207: |
Ehrlich-Sachs Reaction / 208: |
Einhorn Acylation / 209: |
Einhorn-Brunner Reaction / 210: |
Eisleb Alkylation / 211: |
Elbs Persulfate Oxidation / 212: |
Elbs Reaction / 213: |
Eltekoff Hydrolysis / 214: |
Emde Degradation / 215: |
Emmert Reaction / 216: |
Erlenmeyer-plochl Azlactone Synthesis / 217: |
Eschenmoser Coupling / 218: |
Eschenmoser Fragmentation / 219: |
Eschweiler-Clarke Methylation / 220: |
Ester Pyrolysis / 221: |
E´ tard Reaction / 222: |
Evans Aldol Reaction / 223: |
Favorskii Rearrangement / 224: |
Favorskii-Babayan Reaction / 225: |
Feist-Benary Reaction / 226: |
Fenton Reaction / 227: |
Ferrier Reaction / 228: |
Ferrier-II Rearrangement / 229: |
F´etizon Oxidation / 230: |
Finkelstein Reaction / 231: |
Fischer Carbene Complexes / 232: |
Fischer Indole Synthesis / 233: |
Fischer Oxazole Synthesis / 234: |
Fischer Phenylhydrazine Synthesis / 235: |
Fischer Phenylhydrazone and Osazone Synthesis / 236: |
Fischer-Helferich Glycosylation / 237: |
Fischer-Hepp Rearrangement / 238: |
Fischer-Speier Esterification / 239: |
Fischer-Tropsch Synthesis / 240: |
Fleming-Tamao Oxidation / 241: |
Flood Reaction / 242: |
Forster Reaction / 243: |
Franchimont Condensation / 244: |
Frankland Reaction / 245: |
Fr´ater-Seebach Alkylation / 246: |
Freund Reaction / 247: |
Friedel-Crafts Acylation / 248: |
Friedel-Crafts Alkylation / 249: |
Friedl¿ander Condensation / 250: |
Fries Rearrangement / 251: |
Fritsch-Buttenberg-Wiechell Rearrangement / 252: |
Fujimoto-Belleau Reaction / 253: |
Fukuyama Amine Synthesis / 254: |
Fukuyama Indole Synthesis / 255: |
F¿urstner Indole Synthesis / 256: |
Gabriel Primary Amine Synthesis / 257: |
Gabriel Reaction / 258: |
Gabriel-Colman Rearrangement / 259: |
Garner Aldehyde / 260: |
Gassman Indole Synthesis / 261: |
Gassman Oxindole Synthesis / 262: |
Gassman Reaction / 263: |
Gattermann Aldehyde Synthesis / 264: |
Gattermann Reaction / 265: |
Gattermann-Koch Formylation / 266: |
Gewald Reaction / 267: |
Ghosez Cyclization / 268: |
Ghosez Keteniminium-Olefin Cyclization / 269: |
Gibbs-Wohl Naphthalene Oxidation / 270: |
Gilman-Cason Ketone Synthesis / 271: |
Gilman-Speeter Reaction / 272: |
Gomberg Free Radical Reaction / 273: |
Gomberg-Bachmann Pinacol Synthesis / 274: |
Gomberg-Bachmann Reaction / 275: |
Gould-Jacobs Reaction / 276: |
Graebe-Ullmann Synthesis / 277: |
Gr¿anacher Synthesis / 278: |
Gribble Reductive Amination / 279: |
Griess Diazotization / 280: |
Grignard Degradation / 281: |
Grignard Reaction / 282: |
Grob Fragmentation / 283: |
Grosheintz-Fischer-Reissert Aldehyde Synthesis / 284: |
Grundmann Aldehyde Synthesis / 285: |
Gryszkiewicz-Trochimowski and Mccombie Fluorination / 286: |
Guareschi Reaction / 287: |
Guerbet Condensation / 288: |
Gutknecht Condensation / 289: |
Hajos-Parrish-Eder-Sauer-Wiechert Reaction / Part 2: |
Haller-Bauer Cleavage / 291: |
Hammick Reaction / 292: |
Hansley-Prelog Acyloin Condensation / 293: |
Hantzsch Dihydropyridine Synthesis / 294: |
Hantzsch Pyrrole Synthesis / 295: |
Hantzsch Thiazole Synthesis / 296: |
Hass-Bender Oxidation / 297: |
Haworth Methylation / 298: |
Haworth Synthesis / 299: |
Hayashi Rearrangement / 300: |
Heck Reaction / 301: |
Hegedus Indole Synthesis / 302: |
Helferich Condensation / 303: |
Helferich Glycosylation / 304: |
Hell-Volhard-Zelinsky Reaction / 305: |
Hemetsberger Indole Synthesis / 306: |
Henkel Reaction / 307: |
Henry Reaction / 308: |
Herbst-Engel Transamination / 309: |
Heron Rearrangement / 310: |
Herz Reaction / 311: |
Heumann Indigo Process / 312: |
Heyns Rearrangement / 313: |
Hilbert-Johnson Reaction / 314: |
Hinsberg Oxindole Synthesis / 315: |
Hinsberg Reaction / 316: |
Hinsberg Sulfone Synthesis / 317: |
Hinsberg Thiophene Synthesis / 318: |
Hiyama Coupling / 319: |
Hoch-Campbell Reaction / 320: |
Hock Rearrangement / 321: |
Hofer-Moest Reaction / 322: |
Hofmann Degradation / 323: |
Hofmann Elimination / 324: |
Hofmann Isonitrile Synthesis / 325: |
Hofmann Rule / 326: |
Hofmann-Loffler-Freytag Reaction / 327: |
Hofmann-Martius Rearrangement / 328: |
Hofmann-Sand Reaction / 329: |
Hooker Oxidation / 330: |
Horenstein-P¿ahlicke Reaction / 331: |
Horner-Wadsworth-Emmons Olefination / 332: |
Hosomi-Sakurai Allylation / 333: |
Houben-Hoesch Reaction / 334: |
Houdry Cracking Process / 335: |
Huisgen Pyrrole Synthesis / 336: |
Hunsdiecker Condensation / 337: |
Hunsdiecker Reaction / 338: |
Hydroformylation / 339: |
Iodolactonization / 340: |
Irvine-Purdie Methylation / 341: |
Jacobsen Rearrangement / 342: |
Jacobsen-Katsuki Epoxidation / 343: |
Janovsky Reaction / 344: |
Japp-Klingemann Fischer Indole Synthesis / 345: |
Japp-Klingemann Reaction / 346: |
Japp-Maitland Condensation / 347: |
Johnson Orthoester Claisen Rearrangement / 348: |
Jones Oxidation / 349: |
Jourdan-Ullmann Reaction / 350: |
Julia Olefination / 351: |
Juli´a-Colonna Asymmetric Epoxidation / 352: |
Kabachnik-Fields Reaction / 353: |
Kahne Glycosylation / 354: |
Keck Allylation / 355: |
Keck Macrolactonization / 356: |
Kemp Elimination / 357: |
Kennedy Oxidative Cyclization / 358: |
Kiliani-Fischer Cyanohydrin Synthesis / 359: |
Kishner Decomposition / 360: |
Knoevenagel Condensation / 361: |
Knoevenagel Diazotization Method / 362: |
Knorr Pyrazole Synthesis / 363: |
Knorr Pyrrole Synthesis / 364: |
Knorr Quinoline Synthesis / 365: |
Koch-Haaf Carboxylation / 366: |
Kochi Reaction / 367: |
Koenigs-Knorr Reaction / 368: |
Kolbe Electrolysis / 369: |
Kolbe Nitrile Synthesis / 370: |
Kolbe-Schmidt Reaction / 371: |
Kondrat'eva Pyridine Synthesis / 372: |
Kornblum Oxidation / 373: |
Kornblum-Delamare Rearrangement / 374: |
Kostanecki-Robinson Reaction / 375: |
Kowalski Ester Homologation / 376: |
Krapcho Decarboxylation / 377: |
Kriewitz Condensation / 378: |
Kr¿ohnke Pyridine Synthesis / 379: |
Kuhn-Roth Oxidation / 380: |
Kuhn-Winterstein Reduction / 381: |
Kulinkovich Cyclopropanation / 382: |
Kutscheroff Acetylene Hydration / 383: |
Lander Rearrangement / 384: |
Larock Indole Synthesis / 385: |
Lawesson's Reagent / 386: |
Lebedev Process / 387: |
Lehmstedt-Tanasescu Reaction / 388: |
Lemieux-Johnson Oxidation / 389: |
Leuckart Reaction / 390: |
Leuckart Thiophenol Synthesis / 391: |
Levinstein Process / 392: |
Lieben Iodoform Reaction / 393: |
Liebeskind-Srogl Cross-Coupling / 394: |
Lindlar Hydrogenation / 395: |
Lobry de Bruyn-Alberda van Ekenstein Transformation / 396: |
Lombardo Methylenation / 397: |
Lossen Rearrangement / 398: |
Luche Reaction / 399: |
Luche Reduction / 400: |
MacDonald-Fischer Degradation / 401: |
Madelung Indole Synthesis / 402: |
Maillard Reaction / 403: |
Maitland-Japp Reaction / 404: |
Majetich Annulation / 405: |
Malaprade Reaction / 406: |
Malonic Ester Synthesis / 407: |
Mandelic Acid Synthesis / 408: |
Mannich Reaction / 409: |
Marckwald Asymmetric Synthesis / 410: |
Markownikoff Rule and Anti-Markownikoff Rule / 411: |
Martinet Reaction / 412: |
Martin's Sulfurane / 413: |
Mattox-Kendall Reaction / 414: |
McCormack Cycloaddition / 415: |
McFadyen-Stevens Reaction / 416: |
McLafferty Rearrangement / 417: |
McMurry Coupling / 418: |
Meerwein Arylation / 419: |
Meerwein-Ponndorf-Verley Reduction / 420: |
Meerwein's Salt / 421: |
Meinwald Rearrangement / 422: |
Meisenheimer Complexes / 423: |
Meisenheimer Rearrangement / 424: |
Menke Nitration / 425: |
Menschutkin Reaction / 426: |
Mentzer Pyrone Synthesis / 427: |
Merrifield Solid-Phase Peptide Synthesis / 428: |
Meyer-Hartmann Reaction / 429: |
Meyers Aldehyde Synthesis / 430: |
Meyer-Schuster Rearrangement / 431: |
Michael Addition / 432: |
Michaelis-Arbuzov Rearrangement / 433: |
Michael-Stetter Reaction / 434: |
Miescher Degradation / 435: |
Mignonac Reaction / 436: |
Milas Hydroxylation / 437: |
Mislow-Evans Rearrangement / 438: |
Mitsunobu Reaction / 439: |
Moffatt-Swern Oxidation / 440: |
Moore Cyclization / 441: |
Morgan-Walls Cyclization / 442: |
Mori-Ban Indole Synthesis / 443: |
Morin Rearrangement / 444: |
Mosher's Acid / 445: |
Moureau-Mignonac Ketimine Synthesis / 446: |
Mukaiyama Aldol Reaction / 447: |
Mukaiyama-Michael Reaction / 448: |
M¿ uller-Cunradi-Pieroh Process / 449: |
Myers-Saito Cyclization / 450: |
Nagata Reaction / 451: |
Nazarov Cyclization / 452: |
Neber Rearrangement / 453: |
Neber-Bossel Synthesis / 454: |
Nef Reaction / 455: |
Negishi Cross-Coupling / 456: |
Nencki Reaction / 457: |
Nenitzescu Synthesis / 458: |
Nenitzescu Indole Synthesis / 459: |
Newman-Kwart Rearrangement / 460: |
Nicholas Reaction / 461: |
Niementowski Reaction / 462: |
Nierenstein Reaction / 463: |
Norrish Type I Reaction / 464: |
Norrish Type II Reaction / 465: |
Noyori Hydrogenation / 466: |
Nozaki-Hiyama-Kishi Reaction / 467: |
Nysted Reagent / 468: |
Ohle Quinoxaline Synthesis / 469: |
Oppenauer Oxidation / 470: |
Orton Rearrangement / 471: |
Ostromislensky Process / 472: |
Overman Rearrangement / 473: |
Paal-Knorr Furan Synthesis / 474: |
Paal-Knorr Pyrrole Synthesis / 475: |
Paneth Technique / 476: |
Parham Cyclization / 477: |
Parikh-Doering Oxidation / 478: |
Passerini Reaction / 479: |
Paterno-Buchi Reaction / 480: |
Pauson-Khand Reaction / 481: |
Payne Rearrangement / 482: |
Pearlman's Catalyst / 483: |
Pechmann Pyrazole Synthesis / 484: |
Pechmann Reaction / 485: |
Pellizzari Reaction / 486: |
Perkin Reaction / 487: |
Perkin Synthesis / 488: |
Perkow Reaction / 489: |
Petasis-Ferrier Rearrangement / 490: |
Peterson Olefination / 491: |
Petrenko-Kritschenko Piperidone Synthesis / 492: |
Pfau-Plattner Azulene Synthesis / 493: |
Pfitzinger Reaction / 494: |
Pfitzner-Moffatt Oxidation / 495: |
Phillips-Ladenburg Benzimidazole Synthesis / 496: |
Photo-Fries Rearrangement / 497: |
Pictet-Gams Synthesis / 498: |
Pictet-Spengler Reaction / 499: |
Piloty-Robinson Pyrrole Synthesis / 500: |
Pinacol Coupling Reaction / 501: |
Pinacol Rearrangement / 502: |
Pinner Condensation / 503: |
Pinner Reaction / 504: |
Pinner S-Triazine Synthesis / 505: |
Piria Reaction / 506: |
Plancher Rearrangement / 507: |
Polonovski Reaction / 508: |
Pomeranz-Fritsch Reaction / 509: |
Ponzio Reaction / 510: |
Pr´evost Reaction / 511: |
Prey Ether Cleavage / 512: |
Prilezhaev Reaction / 513: |
Prins Reaction / 514: |
Pudovik Reaction / 515: |
Pummerer Rearrangement / 516: |
Quelet Reaction / 517: |
Radziszewski Reaction / Part THREE.: |
Ramberg-B¿acklund Reaction / 519: |
Raney Nickel / 520: |
Rauhut-Currier Reaction / 521: |
Reed Reaction / 522: |
Reformatsky Reaction / 523: |
Regitz Diazo Transfer / 524: |
Reilly-Rickinbottom Rearrangement / 525: |
Reimer-Tiemann Reaction / 526: |
Reissert Compound / 527: |
Reissert Indole Synthesis / 528: |
Reppe Alkyne Cyclotrimerization / 529: |
Reppe Carbonylation / 530: |
Reppe Cyclization / 531: |
Reppe Vinylation / 532: |
Retro-Diels-Alder Reaction / 533: |
Retro-Ene Reaction / 534: |
Retropinacol Rearrangement / 535: |
Reverdin Rearrangement / 536: |
Riehm Quinoline Synthesis / 537: |
Rieke Metal / 538: |
Riemenschneider Reaction / 539: |
Riley Oxidation / 540: |
Ritter Reaction / 541: |
Robinson Annulation / 542: |
Robinson-Gabriel Oxazole Synthesis / 543: |
Robinson-Schopf Condensation / 544: |
Rosenmund Reaction / 545: |
Rosenmund Reduction / 546: |
Rosenmund-von Braun Reaction / 547: |
Rothemund Reaction / 548: |
Roush Crotylboration / 549: |
Rowe Rearrangement / 550: |
Rubottom Oxidation / 551: |
Ruff Degradation / 552: |
Rupe Rearrangement / 553: |
Sabatier-Senderens Reduction / 554: |
Saegusa Cyclization / 555: |
Saegusa Oxidation / 556: |
Sandmeyer Isatin Synthesis / 557: |
Sandmeyer Reaction / 558: |
Sarett Oxidation / 559: |
Saytzeff Rule / 560: |
Schiff Base / 561: |
Schlack-Kumpf Reaction / 562: |
Schlotterbeck Reaction / 563: |
Schmidlin Ketene Synthesis / 564: |
Schmidt Glycosylation / 565: |
Schmidt Reaction / 566: |
Schmidt-Rutz Reaction / 567: |
Schmittel Cyclization / 568: |
Scholl Reaction / 569: |
Sch¿ollkopf Bis-Lactim Ether Method / 570: |
Sch¿ollkopf Oxazole Synthesis / 571: |
Sch¿onberg Rearrangement / 572: |
Schotten-Baumann Reaction / 573: |
Schwartz Reagent / 574: |
Screttas Lithiation / 575: |
Selenoxide Elimination / 576: |
Semmler-Wolff Aromatization / 577: |
Serini Reaction / 578: |
Seyferth-Gilbert Homologation / 579: |
Shapiro Reaction / 580: |
Sharpless Aminohydroxylation / 581: |
Sharpless Dihydroxylation / 582: |
Sharpless Epoxidation / 583: |
Shechter-Kaplan Oxidative Nitration / 584: |
Shi Epoxidation / 585: |
Simmons-Smith Reaction / 586: |
Simonini Reaction / 587: |
Skraup Reaction / 588: |
Smiles Rearrangement / 589: |
Sommelet Reaction / 590: |
Sommelet-Hauser Rearrangement / 591: |
Sonn-Muller Reaction / 592: |
Sonogashira Coupling / 593: |
Staudinger [2+2] Cycloaddition / 594: |
Staudinger Reaction / 595: |
Stec Reaction / 596: |
Steglich Catalyst / 597: |
Steglich Rearrangement / 598: |
Stephen Reaction / 599: |
Stetter Reaction / 600: |
Stevens Rearrangement / 601: |
Stieglitz Rearrangement / 602: |
Stille Coupling / 603: |
Stobbe Condensation / 604: |
Stolle-Becker Synthesis / 605: |
Stork Reaction / 606: |
Strecker Degradation / 607: |
Strecker Reaction / 608: |
Strecker Synthesis / 609: |
Su´arez Cleavage / 610: |
Sugasawa Indole Synthesis / 611: |
Sugasawa Reaction / 612: |
Sundberg Indole Synthesis / 613: |
Suzuki Coupling / 614: |
Swarts Reaction / 615: |
Takai Olefination / 616: |
Tebbe Olefination / 617: |
ter Meer Reaction / 618: |
Thiele-Winter Acetoxylation / 619: |
Thorpe-Ziegler Cyclization / 620: |
Tiemann Cyanohydrin Amination / 621: |
Tiemann Rearrangement / 622: |
Tiffeneau-Demjanov Ring Expansion / 623: |
Tishchenko Reaction / 624: |
Traube Purine Synthesis / 625: |
Trofimov Reaction / 626: |
Trost Desymmetrization / 627: |
Truce-Smiles Rearrangement / 628: |
Tscherniac-Einhorn Reaction / 629: |
Tsuji-Trost Reaction / 630: |
Twitchell Process / 631: |
Tyrer Process / 632: |
Ueno-Stork Cyclization / 633: |
Ugi Reaction / 634: |
Ullmann Acridine Synthesis / 635: |
Ullmann Coupling / 636: |
Ullmann Diaryl Ether Synthesis / 637: |
Urech Cyanohydrin Method.Synthesis / 638: |
van Slyke Method / 640: |
Varrentrapp Reaction / 641: |
Victor Meyer Reaction / 642: |
Vilsmeier Formylation / 643: |
Vinylcyclopropane Rearrangement / 644: |
Voigt Reaction / 645: |
von Auwers Rearrangement / 646: |
von Braun Cyanogen Bromide Reaction / 647: |
von Braun Degradation / 648: |
von Braun-Rudolf Synthesis / 649: |
von Richter Cinnoline Synthesis / 650: |
von Richter Reaction / 651: |
Vorbr¿uggen Glycosylation / 652: |
Wacker Oxidation / 653: |
Wagner-Jauregg Reaction / 654: |
Wagner-Meerwein Rearrangement / 655: |
Walden Inversion / 656: |
Wallach Rearrangement / 657: |
Weerman Reaction / 658: |
Weidenhagen Synthesis / 659: |
Weinreb Amide Formation / 660: |
Weinreb Ketone Synthesis / 661: |
Weiss-Cook Condensation / 662: |
Weitz-Scheffer Epoxidation / 663: |
Wender Indole Synthesis / 664: |
Wessely-Moser Rearrangement / 665: |
Westphalen Rearrangement / 666: |
Wharton Rearrangement / 667: |
Wibaut-Arens Alkylation / 668: |
Wichterle Reaction / 669: |
Widman-Stoermer Synthesis / 670: |
Wilkinson's Catalyst / 671: |
Willgerodt-Kindler Reaction / 672: |
Williamson Ether Synthesis / 673: |
Wittig Reaction / 674: |
[1,2]-Wittig Rearrangement / 675: |
[2,3]-Wittig Rearrangement / 676: |
Wohl Degradation / 677: |
Wohl-Aue Reaction / 678: |
W¿ohler Synthesis / 679: |
Wohl-Ziegler Bromination / 680: |
Wolff Rearrangement / 681: |
Wolffenstein-B¿oters Reaction / 682: |
Wolff-Kishner Reduction / 683: |
Woodward Cis-Hydroxylation / 684: |
Wurtz Synthesis / 685: |
Wurtz-Fittig Reaction / 686: |
Yamada Coupling / 687: |
Yamaguchi Esterification / 688: |
Zeisel Determination / 689: |
Zelinsky-Stadnikoff Reaction / 690: |
Zempl´en Deacetylation / 691: |
Zerewitinoff Determination / 692: |
Ziegler Alcohol Synthesis / 693: |
Ziegler-Hafner Azulene Synthesis / 694: |
Ziegler-Natta Polymerization / 695: |
Zimmermann Reaction / 696: |
Zincke Disulfide Cleavage / 697: |
Zincke Nitration / 698: |
Zincke Reaction / 699: |
Zincke-Suhl Reaction / 700: |
Zinke Synthesis / 701: |
Appendixes |
Schematic Reaction Index |
Reaction Type Summary |
Summary of Initial Publications on Named Reactions |
Journal Abbreviation |
The Statistics of Reaction Published Years |
Subject Index |