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  2. Horner–Wadsworth–Emmons reaction - Wikipedia

    en.wikipedia.org/wiki/HornerWadsworthEmmons...

    The mechanism of the Horner-Wadsworth-Emmons reaction. The ratio of alkene isomers 5 and 6 is not dependent upon the stereochemical outcome of the initial carbanion addition and upon the ability of the intermediates to equilibrate. The electron-withdrawing group (EWG) alpha to the phosphonate is necessary for the final elimination to occur.

  3. Triethyl phosphonoacetate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphonoacetate

    Triethyl phosphonoacetate is a reagent for organic synthesis used in the Horner-Wadsworth-Emmons reaction (HWE) or the Horner-Emmons modification. Triethyl phosphonoacetate can be added dropwise to sodium methoxide solution to prepare a phosphonate anion. It has an acidic proton that can easily be abstracted by a weak base.

  4. William D. Emmons - Wikipedia

    en.wikipedia.org/wiki/William_D._Emmons

    William D. Emmons (November 18, 1924 – December 8, 2001) was an American chemist and published with William S. Wadsworth a modification to the Wittig-Horner reaction using phosphonate-stabilized carbanions, now called the Horner-Wadsworth-Emmons reaction in his honor.

  5. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Wittig–Horner reaction; Wohl degradation; Wohl–Aue reaction; Wohler synthesis; Wohl–Ziegler reaction; Wolffenstein–Böters reaction; Wolff rearrangement; Wolff–Kishner reduction; Woodward cis-hydroxylation; Woodward–Hoffmann rule; Wulff–Dötz reaction; Wurtz coupling, Wurtz reaction; Wurtz–Fittig reaction

  6. Perkow reaction - Wikipedia

    en.wikipedia.org/wiki/Perkow_reaction

    In the related Michaelis–Arbuzov reaction the same reactants are known to form a beta-keto phosphonate which is an important reagent in the HornerWadsworthEmmons reaction on the road to alkenes. The Perkow reaction, in this respect is considered a side-reaction.

  7. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    Ordinarily, the HornerWadsworthEmmons reaction provides the (E)-enoate (α,β-unsaturated ester), just as the Wittig reaction does. To obtain the (Z)-enolate, the Still-Gennari modification of the Horner-Wadsworth-Emmons reaction can be used.

  8. File:Horner-Wadsworth-Emmons reaction example.svg - Wikipedia

    en.wikipedia.org/wiki/File:Horner-Wadsworth...

    Réaction de Horner-Wadsworth-Emmons; Usage on it.wikipedia.org Reazione di Horner-Wadsworth-Emmons; Usage on it.wikibooks.org Chimica organica/Cose da fare; Usage on ja.wikipedia.org ホーナー・ワズワース・エモンズ反応; Usage on nl.wikipedia.org Horner-Wadsworth-Emmons-reactie; Usage on pt.wikipedia.org Reação de Horner ...

  9. Mode of action - Wikipedia

    en.wikipedia.org/wiki/Mode_of_action

    A mechanism of action of a chemical could be "binding to DNA" while its broader mode of action would be "transcriptional regulation". [3] However, there is no clear consensus and the term mode of action is also often used, especially in the study of pesticides, to describe molecular mechanisms such as action on specific nuclear receptors or ...