Search results
Results from the WOW.Com Content Network
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.
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 ...
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.
You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.
Reação de Horner-Wadsworth-Emmons Metadata This file contains additional information, probably added from the digital camera or scanner used to create or digitize it.
Horner-Wadsworth-Emmons-Reaktion; Usage on es.wikipedia.org Reacción de Horner–Wadsworth–Emmons; Usage on pl.wikipedia.org Wikipedysta:Caspel2509/Reakcja Hornera–Wadswortha–Emmonsa; Usage on zh.wikipedia.org 霍纳-沃兹沃思-埃蒙斯反应
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.
Molecular simplification began first by disconnecting both carbon chains with a Wittig reaction and Horner-Wadsworth Emmons modification. The Wittig reaction affords the cis product, while the Horner-Wadsworth Emmons produces the trans olefin. The published synthesis reveals a 1:1 diastereomeric mixture of the carbonyl reduction using zinc ...