enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 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

  3. 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 ...

  4. Wittig reagents - Wikipedia

    en.wikipedia.org/wiki/Wittig_reagents

    Wittig reagents are usually described as a combination of two resonance structures: Ph 3 P + CR 2 − ↔ Ph 3 P=CR 2 The former is called the ylide form and the latter is called the phosphorane form, which is the more familiar representation.

  5. 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).

  6. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Schlosser modification; Schlosser variant; Schmidlin ketene synthesis; Schmidt degradation; Schmidt reaction; Scholl reaction; Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction; Schotten–Baumann reaction; Seliwanoff's test; Semidine rearrangement; Semmler–Wolff reaction; Seyferth–Gilbert homologation; Shapiro reaction

  7. 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.

  8. The Clitoris And The Body - The Huffington Post

    projects.huffingtonpost.com/projects/cliteracy/...

    From ancient history to the modern day, the clitoris has been discredited, dismissed and deleted -- and women's pleasure has often been left out of the conversation entirely. Now, an underground art movement led by artist Sophia Wallace is emerging across the globe to challenge the lies, question the myths and rewrite the rules around sex and the female body.

  9. 2,3-Wittig rearrangement - Wikipedia

    en.wikipedia.org/wiki/2,3-Wittig_rearrangement

    The [1,2]-Wittig rearrangement, which produces isomeric pent-5-en-1-ols, is a competitive process that takes place at high temperatures. [2] Because of the high atom economy and stereoselectivity of the [2,3]-rearrangement, it has gained considerable synthetic utility.