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有机化学人名反应


Acetoacetic Ester Condensation Acetoacetic Ester Synthesis Acyloin Condensation Alder-Ene Reaction Aldol Addition Aldol Condensation Appel Reaction Arbuzov Reaction Arndt-Eistert Synthesis Az

ide-Alkyne 1,3-Dipolar Cycloaddition Azo Coupling b Baeyer-Villiger Oxidation Baker-Venkataraman Rearrangement Balz-Schiemann Reaction Bamford-Stevens Reaction Barton Decarboxylation Barton-McCombie Reaction (Barton Desoxygenation) Baylis-Hillman Reaction Beckmann Rearrangement Benzilic Acid Rearrangement Benzoin Condensation Bergman Cyclization Bestmann-Ohira Reagent Biginelli Reaction Birch Reduction Bischler-Napieralski Reaction Blaise Reaction Blanc Reaction Bohlmann-Rahtz Pyridine Synthesis Boronic Acid Mannich Reaction Bouveault-Blanc Reduction Brook Rearrangement Brown Hydroboration Bucherer-Bergs Reaction Buchwald-Hartwig Cross Coupling Reaction c Cadiot-Chodkiewicz Coupling Cannizzaro Oxidation Reduction CBS Reduction Chan-Lam Coupling Claisen Condensation Claisen Rearrangement Clemmensen Reduction

Click Chemistry Collins Reagent Cope Elimination Cope Rearrangement Conia-Ene Reaction Corey-Bakshi-Shibata Reduction Corey-Chaykovsky Reaction Corey-Fuchs Reaction Corey-Kim Oxidation Corey-Seebach Reaction Corey-Suggs Reagent Corey-Winter Olefin Synthesis Coumarin Synthesis Criegee Mechanism for Ozonolysis Cross Metathesis Curtius Rearrangement (Reaction) d Dakin Reaction Darzens Condensation Darzens Reaction Delépine Reaction Dess-Martin Oxidation Diazotisation Dieckmann Condensation Diels-Alder Reaction 1,3-Dipolar Cycloaddition Directed ortho Metalation Doebner Modification e Eglinton Reaction Ene Reaction Enyne Metathesis Epoxidation Eschweiler-Clarke Reaction Ester Pyrolysis Esterification f Favorskii Reaction Finkelstein Reaction Fischer Esterification Fischer Indole Synthesis Fleming-Tamao Oxidation Friedel-Crafts Acylation Friedel-Crafts Alkylation

Friedlaender Synthesis Fries Rearrangement Fukuyama Coupling Fukuyama Reduction g Gabriel Synthesis Gewald Reaction Glaser Coupling Griesbaum Coozonolysis Grignard Reaction Grubbs Reaction h Haloform Reaction Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis) Hay Coupling Heck Reaction Hell-Volhard-Zelinsky Reaction Henry Reaction Hiyama Coupling Hiyama-Denmark Coupling Hofmann Elimination Hofmann's Rule Horner-Wadsworth-Emmons Reaction Hosomi-Sakurai Reaction Huisgen Cycloaddition Hunsdiecker Reaction Hydroboration i Ireland-Claisen Rearrangement Itsuno-Corey Reduction Iwanow Reaction (Reagent) j Jacobsen Epoxidation Jacobsen-Katsuki Epoxidation Jocic Reaction Johnson-Corey-Chaykovsky Reaction Jones Oxidation Julia-Lythgoe Olefination Julia-Kocienski Olefination k Kabachnik-Fields Reaction Kindler Reaction Knoevenagel Condensation Kochi Reaction

Kolbe Electrolysis Kolbe Nitrile Synthesis Kolbe-Schmitt Reaction Kulinkovich Reaction Kulinkovich-de Meijere Reaction Kulinkovich-Szymoniak Reaction Kumada Coupling l Lawesson's Reagent Leuckart Thiophenol Reaction Luche Reduction m Malonic Ester Synthesis Mannich Reaction Markovnikov's Rule McMurry Reaction Meerwein-Ponndorf-Verley Reduction Myers' Modification of the Ramberg-B?cklund Reaction Myers-Saito Cyclization Michael Addition Michaelis-Arbuzov Reaction Mitsunobu Reaction Miyaura Borylation Reaction Modified Julia Olefination Mukaiyama Aldol Addition n Nazarov Cyclization Nef Reaction Negishi Coupling Newman-Kwart Rearrangement Nitroaldol Reaction Nozaki-Hiyama Coupling Nucleophilic Substitution (SN1 / SN2) o Ohira-Bestmann Reagent Olefin Metathesis Oppenauer Oxidation Overman Rearrangement Oxy-Cope Rearrangement Ozonolysis p Paal-Knorr Furan Synthesis Paal-Knorr Pyrrole Synthesis Paal-Knorr Thiophene Synthesis

Passerini Reaction Paterno-Büchi Reaction Pauson-Khand Reaction Pechmann Condensation Petasis Reaction Peterson Olefination Pinacol Coupling Reaction Pinacol Rearrangement Pinner Reaction Prévost Reaction Prilezhaev Reaction Prins Reaction Pschorr Reaction q r Ramberg-B?cklund Reaction Reformatsky Reaction Ring Closing Metathesis Ring Opening Metathesis (Polymerization) Ritter Reaction Robinson Annulation Rosenmund Reduction Rosenmund-von Braun Reaction Rubottom Oxidation s Sakurai Reaction Sandmeyer Reaction Saytzeff's Rule Schiemann Reaction Schlosser Modification Schmidt Reaction Schotten-Baumann Reaction Seebach Umpolung Seyferth-Gilbert Homologation Sarett Reagent Shapiro Reaction Sharpless Aminohydroxylation Sharpless Dihydroxylation Sharpless Epoxidation Shi Epoxidation Simmons-Smith Reaction Sonogashira Coupling Staudinger Cycloaddition Staudinger Reaction

Staudinger Reduction Staudinger Synthesis Steglich Esterification Stetter Reaction Stille Coupling Strecker Synthesis Suzuki Coupling Swern Oxidation t Tamao-Kumada Oxidation Tebbe Olefination Tishchenko Reaction Tsuji-Trost Reaction Trost Allylation u Ugi Reaction Ullmann Reaction Upjohn Dihydroxylation v Van Leusen Imidazole Synthesis Van Leusen Oxazole Synthesis Van Leusen Reaction Vicarious Nucleophilic Substitution Vilsmeier Reaction w Wacker-Tsuji Oxidation Weinreb Ketone Synthesis Wenker Synthesis Willgerodt-Kindler Reaction Williamson Synthesis Wittig-Horner Reaction Wittig Reaction [1,2]-Wittig Rearrangement [2,3]-Wittig Rearrangement Wohl-Ziegler Reaction Wolff-Kishner Reduction Wolff Rearrangement Woodward cis-Hydroxylation Woodward Reaction Wurtz Reaction Wurtz-Fittig Reaction x y Yamaguchi Esterification


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