Organic Reactions, Condensed or Abridged

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In the near future, these contents will be organized into sections based on the type of reaction. For now, they are presented in alphabetical order.

2+2 photocycloaddition
2,3-Wittig rearrangement
4+3 cycloaddition
6+4 cycloaddition
Abramov reaction
Allylic stannane addition
Alpha-ketol rearrangement
Asymmetric ester hydrolysis with pig liver esterase
Asymmetric nucleophilic epoxidation
Base-promoted epoxide isomerization
Benzylic activation and stereocontrol in tricarbonyl(arene)chromium complexes
Carbonyl oxidation with hypervalent iodine reagents
Desulfonylation reactions
Divinylcyclopropane-cycloheptadiene rearrangement
Electrophilic amination
Electrophilic fluorination
Electrophilic substitution of unsaturated silanes
Enantioselective reduction of ketones
Epoxidation with dioxiranes
Fluorination by sulfur tetrafluoride
Fluorination with aminosulfuranes
Heteroatom-promoted lateral lithiation
Hydrocyanation of unsaturated carbonyl compounds
Hydrogenation of carbon-nitrogen double bonds
Imine Diels-Alder reaction
Intermolecular metal-catalyzed carbenoid cyclopropanations
Intramolecular Heck reaction
Intramolecular reactions of diazocarbonyl compounds
Ketene cycloaddition
Manganese-mediated coupling reactions
Microbial arene oxidation
Nitrone-olefin 3+2 cycloaddition
Oxidation with chromium(VI)-amine complexes
Oxidation with dioxiranes
Oxoammonium-catalyzed oxidation
Payne rearrangement
Phenol oxidation with hypervalent iodine reagents
Radical cyclization
Reactions of alkenyl- and alkynylaluminum compounds
Reactions of nitrile anions
Reactions of organoborates and boranes
Reactions of organocopper reagents
Reductions with diimide
Reductions with hydrosilanes
Reductions with metal alkoxyaluminum hydrides
Reductions with samarium(II) iodide
Reductive dehalogenation of halo ketones
Retro Diels-Alder reaction
Selenoxide elimination
Stilbene photocylization
Synthesis of nucleosides
Trimethylenemethane cycloaddition
Vicinal difunctionalization