List of name reactions
Here is a list of many named reactions. The detailed mechanism is provided for each of them and several samples are given to illustrate their synthetic usefulness.
All of theses reactions are taken from our synthesis database and the list is continually growing.
B
Baeyer-Villiger Oxidation
Baker-Venkataraman Rearrangement
Bamford-Stevens Reaction
Bargellini Reaction
Bartoli Indole Synthesis
Barton Decarboxylation
Barton Reaction
Barton Vinyl Iodide Synthesis
Barton-Kellogg Reaction
Barton-McCombie Reaction
Barton-Zard Reaction
Beckmann Rearrangement
Benzilic Acid Rearrangement
Benzoin Condensation
Betti Reaction
Biginelli Reaction
Birch Reduction
Bischler-Napieralski Reaction
Blaise Reaction
Blanc Halomethylation
Bogert-Cook Synthesis
Bohlmann-Rahtz Pyridine Synthesis
Bradsher Cyclization
Brook Rearrangement
Brown Asymmetric Allylation
Buchner Ring Expansion
Buchwald-Hartwig Coupling
Burgess Dehydration
Büchner-Curtius-Schlotterbeck Reaction
C
Cadiot-Chodkiewicz Coupling
Cadogan-Sundberg Indole Synthesis
Casnati-Skattebøl Formylation
Catellani Reaction
Chan Rearrangement
Chan-Evans-Lam Coupling
Charette Asymmetric Cyclopropanation
Chugaev Elimination
Claisen Condensation
Claisen Rearrangement
Claisen-Schmidt Condensation
Clemmensen Reduction
Conrad-Limpach Synthesis
Cope Elimination
Cope Rearrangement
Corey-Fuchs Reaction
Corey-Kim Oxidation
Corey-Nicolaou Macrolactonization
Corey-Posner, Whitesides-House Reaction
Corey-Seebach Reaction
Corey-Winter Olefin Synthesis
Criegee Reaction
Curtius Rearrangement
F
Favorskii Rearrangement
Finkelstein Reaction
Fischer Indole Synthesis
Fischer-Speier Esterification
Fleming-Tamao Oxidation
Forster-Decker Amine Synthesis
Friedel-Crafts Acylation
Friedel-Crafts Alkylation
Friedländer synthesis
Fries Rearrangement
Fritsch-Buttenberg-Wiechell Rearrangement
Fujimoto-Belleau Reaction
Fukuyama Indole Synthesis
H
Haloform Reaction
Hanessian-Hullar Reaction
Hantzsch Thiazole Synthesis
Hass-Bender Oxidation
Hell-Volhard-Zelinsky Reaction
Hemetsberger-Knittel Indole Synthesis
Henry Reaction
Hiyama Coupling
Hofmann Elimination
Hofmann Rearrangement
Hofmann-Löffler-Freytag Reaction
Horner-Wadsworth-Emmons Reaction
Hosomi-Sakurai Reaction
Houben-Hoesch Reaction
Huisgen Cycloaddition
Hunsdiecker Reaction
M
Madelung Indole Synthesis
Maitland-Japp Reaction
Mannich Reaction
Markó-Lam Deoxygenation
McMurry Reaction
Meerwein-Ponndorf-Verley Reduction
Meisenheimer Rearrangement
Meyer-Schuster Rearrangement
Michael Addition
Michaelis-Arbuzov Reaction
Mitsunobu Reaction
Miyaura Borylation
Mizoroki-Heck Reaction
Morita-Baylis-Hillman Reaction
Mukaiyama Aldol Addition
Mukaiyama Hydration
Myers Asymmetric Alkylation
P
Paal-Knorr Furan Synthesis
Paal-Knorr Pyrrole Synthesis
Parikh-Doering Oxidation
Passerini Reaction
Paterno-Büchi Reaction
Pauson-Khand Reaction
Payne Epoxidation
Payne Rearrangement
Pechmann Condensation
Petasis-Ferrier Rearrangement
Peterson Olefination
Petrenko-Kritschenko Piperidone Synthesis
Pfitzner-Moffatt oxidation
Piancatelli Rearrangement
Pictet-Spengler Reaction
Pinacol Coupling
Pinacol Rearrangement
Pinner Reaction
Pinnick-Lindgren Oxidation
Polonovski-Potier Reaction
Pomeranz-Fritsch Isoquinoline Synthesis
Prilezhaev Reaction
Prins Reaction
Pschorr Reaction
Pummerer Rearrangement
S
Saegusa-Ito Oxidation
Sandmeyer Isatin Synthesis
Sandmeyer Reaction
Sarett Oxidation
Schlosser Modification
Schmidt Reaction
Scholl Reaction
Schotten-Baumann Reaction
Semi-Pinacol Rearrangement
Semmler-Wolff Reaction
Seyferth-Gilbert Homologation
Shapiro Reaction
Sharpless Asymmetric Dihydroxylation
Sharpless Epoxidation
Simmons-Smith Reaction
Smiles Rearrangement
Sommelet Reaction
Sonogashira Coupling
Staudinger Reaction
Steglich Esterification
Stetter Reaction
Stevens Rearrangement
Still-Gennari Reaction
Stille Coupling
Stobbe Condensation
Stollé Synthesis
Stork Enamine Synthesis
Suzuki Coupling
Swern Oxidation