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
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
- Davis Oxidation
- 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
- Kowalski Ester Homologation
- 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