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  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. 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.

  4. 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 ...

  5. 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.

  6. 2,3-Wittig rearrangement - Wikipedia

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

    The [2,3]-Wittig rearrangement is the transformation of an allylic ether into a homoallylic alcohol via a concerted, pericyclic process.Because the reaction is concerted, it exhibits a high degree of stereocontrol, and can be employed early in a synthetic route to establish stereochemistry.

  7. Aza-Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Aza-Wittig_reaction

    An example of the aza-Wittig-reaction being utilized in organic synthesis is the synthesis of (–)-benzomalvin A. Two intramolecular aza-Wittig-reactions were used to construct the seven-membered ring and the six-membered ring in the molecule's skeleton. [1] Synthesis of (−)-Benzomalvin A via multiple aza-Wittig-reactions

  8. Schlosser variant - Wikipedia

    en.wikipedia.org/?title=Schlosser_variant&...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Schlosser_variant&oldid=49613304"This page was last edited on 22 April 2006, at 16:47 (UTC). (UTC).

  9. Western Forge - Wikipedia

    en.wikipedia.org/wiki/Western_Forge

    Western Forge was founded in Defiance, Ohio in 1965 as a joint venture between Sears and C. William Schlosser to make torque wrenches. [3] In 1966, it relocated to Colorado Springs, Colorado , where it built a new manufacturing facility.