3.1 [m+n]-Cycloaddition Reactions (Excluding [4+2])
3.2 [4+2]-Cycloaddition Reactions
3.3 [m+n+1]-Carbocyclization Reactions
3.4 [m+n+2]-Carbocyclization Reactions
3.5 Asymmetric Cycloisomerizations
3.6 Ene Reactions
3.7 Sigmatropic Rearrangements
3.8 Electrocyclic Reactions
3.9 Allylic Substitution Reactions
3.10 Isomerizations To Form a Stereogenic Center and Allylic Rearrangements
3.11 Allylic and Benzylic Oxidation
3.12 Mizoroki–Heck Reaction
3.13 C—C Bond Formation by C—H Bond Activation
3.14 Cross Coupling
3.15 Protonation, Alkylation, Arylation, and Vinylation of Enolates
3.16 Α-Functionalization of Carbonyl Compounds
3.17 Baeyer–Villiger Reactions
3.18 Ring Opening of Epoxides, Aziridines, and Cyclic Anhydrides
3.19 Acylation of Alcohols and Amines
3.20 Asymmetric Fluorination, Monofluoromethylation, Difluoromethylation, and Trifluoromethylation Reactions
3.21 Stereoselective Polymerization
3.22 Oxidation of Sulfides
