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A
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
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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
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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)
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D
Dakin Reaction Darzens Condensation Darzens Reaction De Kimpe Aziridine Synthesis 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 Koser's Reagent 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-Bäcklund 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
O'Donnell Amino Acid Synthesis 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-Bäcklund 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

z