Mevans86

Hey Wikipedia! I'm a graduate student working to bring the lesser known side of organic chemical reactivity to Wikipedia. Feel free to drop a line on my Talk page.

Live Pages Organic Reactions 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