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  2. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    Download as PDF; Printable version; In other projects ... In organic chemistry, alkynylation is an addition reaction in which a terminal alkyne (−C≡CH ...

  3. Asymmetric addition of alkynylzinc compounds to aldehydes

    en.wikipedia.org/wiki/Asymmetric_Addition_of...

    This alkynylation reaction is enantioselective and involves an alkynylzinc reagent [1] rather than the sodium acetylide used by John Ulric Nef in his 1899 report of the synthetic approach. [ 2 ] [ 3 ] Propargyl alcohols are versatile precursors for the chirally-selective synthesis of natural products and pharmaceutical agents , making this ...

  4. File:Alkynylation.svg - Wikipedia

    en.wikipedia.org/wiki/File:Alkynylation.svg

    English: Diagram showing the chemical reaction involving Sonogashira reaction of a phenylalanine derivative with an alkyne. Modified from File:Alkynylation.gif to correct chemical errors. Date

  5. Alkyne zipper reaction - Wikipedia

    en.wikipedia.org/wiki/Alkyne_zipper_reaction

    The alkyne zipper reaction is an organic reaction that involves isomerization of a non terminal alkyne into a terminal alkyne. This reaction was first reported by Alexey Favorsky in 1887 (J. Russ. Phys.-Chem. Soc., 19, 414 (1887)). Also, this reaction was reported by Charles Allen Brown and Ayako Yamashita in 1975. [1]

  6. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.

  7. Corey–Fuchs reaction - Wikipedia

    en.wikipedia.org/wiki/Corey–Fuchs_reaction

    The Corey–Fuchs reaction, also known as the Ramirez–Corey–Fuchs reaction, is a series of chemical reactions designed to transform an aldehyde into an alkyne. [1] [2] [3] The formation of the 1,1-dibromoolefins via phosphine-dibromomethylenes was originally discovered by Desai, McKelvie and Ramirez. [4]

  8. Transition metal alkyne complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkyne...

    When bonded side-on to a single metal atom, an alkyne serves as a dihapto usually two-electron donor. For early metal complexes, e.g., Cp 2 Ti(C 2 R 2), strong π-backbonding into one of the π* antibonding orbitals of the alkyne is indicated.

  9. Seyferth–Gilbert homologation - Wikipedia

    en.wikipedia.org/wiki/Seyferth–Gilbert...

    The Seyferth–Gilbert homologation is a chemical reaction of an aryl ketone 1 (or aldehyde) with dimethyl (diazomethyl)phosphonate 2 and potassium tert-butoxide to give substituted alkynes 3. [ 1 ] [ 2 ] Dimethyl (diazomethyl)phosphonate 2 is often called the Seyferth–Gilbert reagent .