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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. W. Clark Still - Wikipedia

    en.wikipedia.org/wiki/W._Clark_Still

    The Horner-Wadsworth-Emmons reaction is a widely used olefination reaction in which a phosphonate-stabilized carbanion reacts with an aldehyde or ketone to form an alkene. In the standard HWE reaction, the phosphonate ester contains alkoxy substituents (typically methoxy or ethoxy), producing an E -alkene as the major product.

  5. 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.

  6. Strychnine total synthesis - Wikipedia

    en.wikipedia.org/wiki/Strychnine_total_synthesis

    In the final steps a HornerWadsworthEmmons reaction (methyl 2-(diethy1phosphono)acetate) give acrylate ester 12 as a mixture of cis and trans isomers which could be coached into the right (trans) direction by application of light in a photochemical rearrangement, the ester group was reduced (DIBAL / boron trifluoride) to isostrychnine 13 ...

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  9. 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.