enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Horner–Wadsworth–Emmons reaction - Wikipedia

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

    The Horner–Wadsworth–Emmons (HWE) reaction is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes. [1] The Horner–Wadsworth–Emmons reaction. In 1958, Leopold Horner published a modified Wittig reaction using phosphonate-stabilized carbanions.

  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

    Hantzsch pyridine synthesis, Gattermann–Skita synthesis, Guareschi–Thorpe condensation, Knoevenagel–Fries modification; Hantzsch–Collidin synthesis; Harries ozonolysis; Haworth methylation; Haworth Synthesis; Hay coupling; Hayashi rearrangement; Heck reaction; Hegedus indole synthesis; Helferich method; Hell–Volhard–Zelinsky ...

  6. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    Factors governing organic reactions are essentially the same as that of any chemical reaction.Factors specific to organic reactions are those that determine the stability of reactants and products such as conjugation, hyperconjugation and aromaticity and the presence and stability of reactive intermediates such as free radicals, carbocations and carbanions.

  7. File:Lake Ontario food web.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Lake_Ontario_food_web.pdf

    NOAA Great Lakes Food Web Diagrams direct Author NOAA, Great Lakes Environmental Research Laboratory: Mason, Krause, and Ulanowicz, 2002 - Modifications for Lake Ontario, 2009.

  8. Leopold Horner - Wikipedia

    en.wikipedia.org/wiki/Leopold_Horner

    Leopold Horner (24 August 1911 – 5 October 2005) was a German chemist who published a modified Wittig reaction using phosphonate-stabilized carbanions now called the Horner–Wadsworth–Emmons reaction (HWE reaction) or Horner-Wittig reaction.

  9. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    Ordinarily, the Horner–Wadsworth–Emmons 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.