Skip to main content
Chemistry LibreTexts

O-chem Reactions

  • Page ID
    4859
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    2+2 photocycloaddition
    2,3-Wittig rearrangement
    4+3 cycloaddition
    6+4 cycloaddition
    Abramov reaction
    Allylic stannane addition
    Alpha-ketol rearrangement
    Asymmetric deprotonation using chiral lithium amides
    Asymmetric ester hydrolysis with pig liver esterase
    Asymmetric nucleophilic epoxidation
    Aza-Cope/Mannich reaction
    Barton-McCombie reaction
    Base-promoted epoxide isomerization
    Benzylic activation and stereocontrol in tricarbonyl(arene)chromium complexes
    Boronic acid Mannich reaction (Petasis Reaction)
    Carbonyl oxidation with hypervalent iodine reagents
    Catalytic asymmetric ketene cycloadditions
    Catalytic, asymmetric, intramolecular C-H insertion
    Cross-coupling reactions of organotrifluoroborates
    Cycloadditions of carbonyl ylides made from diazocarbonyl compounds
    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 alkenes and alkynes
    Hydrocyanation of unsaturated carbonyl compounds
    Hydrogen-bonding-mediated directed osmium dihydroxylation
    Hydrogenation of carbon-nitrogen double bonds
    Imine Diels-Alder reaction
    Indoles via palladium-catalyzed cyclization
    Intermolecular C-H insertions of carbenoids
    Intermolecular metal-catalyzed carbenoid cyclopropanations
    Intramolecular Heck reaction
    Intramolecular reactions of diazocarbonyl compounds
    Ketene cycloaddition
    Krapcho dealkoxycarbonylation
    Kulinkovich cyclopropanation
    Manganese-mediated coupling reactions
    McMurry coupling
    Microbial arene oxidation
    Neber rearrangement
    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
    Schmidt reaction (2)
    Selenoxide elimination
    Synthesis of nucleosides
    Transition-metal-catalyzed alpha-arylation of enolates
    Trimethylenemethane cycloaddition
    Two-fold extrusion reactions
    Vicinal difunctionalization

    O-chem Reactions is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

    • Was this article helpful?