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240 terms

Organic Name Reactions

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[1,2]-Wittig Rearrangement
[2,3]-Wittig Rearrangement
1,3-Dipolar Cycloaddition
Acetoacetic Ester Condensation
Acetoacetic Ester Synthesis
Acyloin Condensation
Alder-Ene Reaction
Aldol Addition
Aldol Condensation
Appel Reaction
Arbuzov Reaction
Arndt-Eistert Synthesis
Azide-Alkyne 1,3-Dipolar Cycloaddition
Azo Coupling
Baeyer-Villiger Oxidation
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Baker-Venkataraman Rearrangement
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Balz-Schiemann Reaction
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Bamford-Stevens Reaction
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Barton Decarboxylation
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Barton-McCombie Reaction (Barton Desoxygenation)
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Baylis-Hillman Reaction
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Beckmann Rearrangement
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Benzilic Acid Rearrangement
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Benzoin Condensation
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Bergman Cyclization
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Bestmann-Ohira Reagent
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Biginelli Reaction
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Birch Reduction
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Bischler-Napieralski Reaction
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Blaise Reaction
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Blanc Reaction
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Bohlmann-Rahtz Pyridine Synthesis
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Boronic Acid Mannich Reaction
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Bouveault-Blanc Reduction
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Brook Rearrangement
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Brown Hydroboration
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Bucherer-Bergs Reaction
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Buchwald-Hartwig Cross Coupling Reaction
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Cadiot-Chodkiewicz Coupling
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Cannizzaro Oxidation Reduction
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CBS Reduction
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Chan-Lam Coupling
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Claisen Condensation
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Claisen Rearrangement
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Clemmensen Reduction
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Click Chemistry
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Collins Reagent
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Conia-Ene Reaction
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Cope Elimination
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Cope Rearrangement
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Corey-Bakshi-Shibata Reduction
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Corey-Chaykovsky Reaction
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Corey-Fuchs Reaction
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Corey-Kim Oxidation
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Corey-Seebach Reaction
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Corey-Suggs Reagent
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Corey-Winter Olefin Synthesis
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Coumarin Synthesis
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Criegee Mechanism for Ozonolysis
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Cross Metathesis
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Curtius Rearrangement (Reaction)
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Dakin Reaction
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Darzens Condensation
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Darzens Reaction
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Delépine Reaction
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Dess-Martin Oxidation
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Diazotisation
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Dieckmann Condensation
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Diels-Alder Reaction
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Directed ortho Metalation
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Doebner Modification
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Eglinton Reaction
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Ene Reaction
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Enyne Metathesis
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Epoxidation
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Eschweiler-Clarke Reaction
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Ester Pyrolysis
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Esterification
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Favorskii Reaction
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Finkelstein Reaction
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Fischer Esterification
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Fischer Indole Synthesis
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Fleming-Tamao Oxidation
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Friedel-Crafts Acylation
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Friedel-Crafts Alkylation
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Friedlaender Synthesis
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Fries Rearrangement
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***uyama Coupling
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***uyama Reduction
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Gabriel Synthesis
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Gewald Reaction
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Glaser Coupling
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Griesbaum Coozonolysis
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Grignard Reaction
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Grubbs Reaction
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Haloform Reaction
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Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis)
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Hay Coupling
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Heck Reaction
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Hell-Volhard-Zelinsky Reaction
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Henry Reaction
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Hiyama Coupling
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Hiyama-Denmark Coupling
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Hofmann Elimination
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Hofmann's Rule
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Horner-Wadsworth-Emmons Reaction
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Hosomi-Sakurai Reaction
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Huisgen Cycloaddition
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Hunsdiecker Reaction
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Hydroboration
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Ireland-Claisen Rearrangement
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Itsuno-Corey Reduction
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Iwanow Reaction (Reagent)
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Jacobsen Epoxidation
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Jacobsen-Katsuki Epoxidation
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Jocic Reaction
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Johnson-Corey-Chaykovsky Reaction
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Jones Oxidation
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Julia-Kocienski Olefination
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Julia-Lythgoe Olefination
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Kabachnik-Fields Reaction
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Kindler Reaction
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Knoevenagel Condensation
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Kochi Reaction
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Kolbe Electrolysis
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Kolbe Nitrile Synthesis
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Kolbe-Schmitt Reaction
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Kulinkovich Reaction
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Kulinkovich-de Meijere Reaction
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Kulinkovich-Szymoniak Reaction
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Kumada Coupling
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Lawesson's Reagent
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Leuckart Thiophenol Reaction
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Luche Reduction
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Malonic Ester Synthesis
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Mannich Reaction
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Markovnikov's Rule
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McMurry Reaction
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Meerwein-Ponndorf-Verley Reduction
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Michael Addition
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Michaelis-Arbuzov Reaction
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Mitsunobu Reaction
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Miyaura Borylation Reaction
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Modified Julia Olefination
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Mukaiyama Aldol Addition
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Myers' Modification of the Ramberg-Bäcklund Reaction
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Myers-Saito Cyclization
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Nazarov Cyclization
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Nef Reaction
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Negishi Coupling
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Newman-Kwart Rearrangement
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Nitroaldol Reaction
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Nozaki-Hiyama Coupling
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Nucleophilic Substitution (SN1 / SN2)
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Ohira-Bestmann Reagent
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Olefin Metathesis
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Oppenauer Oxidation
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Overman Rearrangement
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Oxy-Cope Rearrangement
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Ozonolysis
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Paal-Knorr Furan Synthesis
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Paal-Knorr Pyrrole Synthesis
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Paal-Knorr Thiophene Synthesis
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Passerini Reaction
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Paterno-Büchi Reaction
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Pauson-Khand Reaction
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Pechmann Condensation
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Petasis Reaction
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Peterson Olefination
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Pinacol Coupling Reaction
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Pinacol Rearrangement
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Pinner Reaction
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Prévost Reaction
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Prilezhaev Reaction
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Prins Reaction
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Pschorr Reaction
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Ramberg-Bäcklund Reaction
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Reformatsky Reaction
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Ring Closing Metathesis
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Ring Opening Metathesis (Polymerization)
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Ritter Reaction
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Robinson Annulation
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Rosenmund Reduction
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Rosenmund-von Braun Reaction
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Rubottom Oxidation
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Sakurai Reaction
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Sandmeyer Reaction
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Sarett Reagent
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Saytzeff's Rule
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Schiemann Reaction
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Schlosser Modification
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Schmidt Reaction
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Schotten-Baumann Reaction
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Seebach Umpolung
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Seyferth-Gilbert Homologation
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Shapiro Reaction
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Sharpless Aminohydroxylation
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Sharpless Dihydroxylation
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Sharpless Epoxidation
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Shi Epoxidation
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Simmons-Smith Reaction
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Sonogashira Coupling
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Staudinger Cycloaddition
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Staudinger Reaction
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Staudinger Reduction
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Staudinger Synthesis
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Steglich Esterification
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Stetter Reaction
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Stille Coupling
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Strecker Synthesis
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Suzuki Coupling
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Swern Oxidation
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Tamao-Kumada Oxidation
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Tebbe Olefination
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Tishchenko Reaction
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Trost Allylation
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Tsuji-Trost Reaction
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Ugi Reaction
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Ullmann Reaction
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Upjohn Dihydroxylation
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Van Leusen Imidazole Synthesis
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Van Leusen Oxazole Synthesis
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Van Leusen Reaction
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Vicarious Nucleophilic Substitution
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Vilsmeier Reaction
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Wacker-Tsuji Oxidation
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Weinreb Ketone Synthesis
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Wenker Synthesis
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Willgerodt-Kindler Reaction
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Williamson Synthesis
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Wittig Reaction
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Wittig-Horner Reaction
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Wohl-Ziegler Reaction
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Wolff Rearrangement
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Wolff-Kishner Reduction
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Woodward Reaction
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Woodward cis-Hydroxylation
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Wurtz Reaction
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Wurtz-Fittig Reaction
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Yamaguchi Esterification
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