When.com Web Search

  1. Ads

    related to: schlosser modification of wittig water line faucet

Search results

  1. Results From The WOW.Com Content Network
  2. Modified Wittig–Claisen tandem reaction - Wikipedia

    en.wikipedia.org/wiki/Modified_Wittig–Claisen...

    Modified Wittig–Claisen tandem reaction is a cascade reaction that combines the Wittig reaction and Claisen rearrangement together. The Wittig reaction generates the allyl vinyl ether intermediate that further participates in a Claisen rearrangement to generate the final γ,δ-unsaturated ketone or aldehyde product (Figure "Modified Wittig ...

  3. Talk:Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Talk:Wittig_reaction

    In order to obtain the E-alkene, the Schlosser modification of the Wittig reaction can be performed." That agrees with the general description in the "Classical mechanism" section, which accompanies the mechanism leading to 7 (a Z form).

  4. Wittig reagents - Wikipedia

    en.wikipedia.org/wiki/Wittig_reagents

    For stabilized Wittig reagents bearing conjugated electron-withdrawing groups, even relatively weak bases like aqueous sodium hydroxide or potassium carbonate can be employed. [Ph 3 PCH 3] + Br −, typical phosphonium salt. The identification of a suitable base is often an important step when optimizing a Wittig reaction.

  5. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    The main limitation of the traditional Wittig reaction is that the reaction proceeds mainly via the erythro betaine intermediate, which leads to the Z-alkene. The erythro betaine can be converted to the threo betaine using phenyllithium at low temperature. [18] This modification affords the E-alkene. The Schlosser variant of the Wittig reaction

  6. 1,2-Wittig rearrangement - Wikipedia

    en.wikipedia.org/wiki/1,2-Wittig_rearrangement

    A 1,2-Wittig rearrangement is a categorization of chemical reactions in organic chemistry, and consists of a 1,2-rearrangement of an ether with an alkyllithium compound. [1] The reaction is named for Nobel Prize winning chemist Georg Wittig. [2] [3] The intermediate is an alkoxy lithium salt, and the final product an alcohol.

  7. Horner–Wadsworth–Emmons reaction - Wikipedia

    en.wikipedia.org/wiki/Horner–Wadsworth–Emmons...

    In 1958, Leopold Horner published a modified Wittig reaction using phosphonate-stabilized carbanions. [2] [3] William S. Wadsworth and William D. Emmons further defined the reaction. [4] [5] In contrast to phosphonium ylides used in the Wittig reaction, phosphonate-stabilized carbanions are more nucleophilic but less basic. Likewise ...

  1. Ads

    related to: schlosser modification of wittig water line faucet