A
Appel Reaction
B
Baeyer-Villiger oxidation
Bartoli indole synthesis
Baylis-Hillman reaction
Beckmann rearrangement
Biginelli reaction
Birch reduction
Buchwald-Hartwig amination
C
Cannizzaro reaction
Claisen condensation
Claisen rearrangement
Clemmensen reduction
Cope rearrangement
Corey-Kim oxidation
Curtius rearrangement
D
Dakin-West reaction
Dieckmann condensation
Diels-Alder reaction
E
Eschenmoser-Claisen rearrangement
Eschweiler-Clarke reaction
F
Finkelstein reaction
Fischer esterification
Fischer indole synthesis
Friedel-Crafts acylation
Friedel-Crafts alkylation
Fries rearrangement
G
Gabriel synthesis
Grignard reaction
H
Heck reaction
Hell-Volhard-Zelinsky reaction
Henry reaction
Hofmann elimination
Hofmann rearrangement
I
Ireland-Claisen rearrangement
J
Johnson-Claisen rearrangement
Jones oxidation
K
Knoevenagel condensation
Knorr pyrazole synthesis
Kolbe-Schmitt reaction
Kumada cross-coupling
L
Luche reduction
M
Mannich reaction
Michael addition
Mitsunobu reaction
Mukaiyama aldol addition
N
Negishi cross-coupling
O
Oppenauer oxidation
P
Pauson-Khand reaction
Perkin reaction
Pictet-Spengler reaction
Prins reaction
Q
R
Reformatsky reaction
Reimer-Tiemann reaction
Ritter reaction
Robinson annulation
S
Sandmeyer reaction
Schmidt reaction
Schotten-Baumann reaction
Sharpless epoxidation
Sonogashira cross-coupling
Staudinger reaction
Stille cross-coupling
Strecker amino acid synthesis
Suzuki cross-coupling
Swern oxidation
T
U
Ullmann reaction
V
Vilsmeier-Haack reaction
W
Wagner-Meerwein rearrangement
Williamson ether synthesis
Wittig reaction
Wolff-Kishner reduction
Wolff rearrangement
Wurtz reaction
X
Y
Yamaguchi esterification
Z
