olefin metathesis wikipedia - EAS

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  1. Olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative organic reactions.
    Organic Chemistry Portal: olefin-metathesis
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    en.wikipedia.org/wiki/Olefin_metathesis
    en.wikipedia.org/wiki/Olefin_metathesis
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    What is the olefin metathesis reaction?
    Tsuji describes the olefin metathesis reaction as “…potentially useful in organic synthesis” and addresses the need for the development of a more versatile catalyst to tolerate various functional groups.
    en.wikipedia.org/wiki/Ring-closing_metathesis
    What is alkyne metathesis?
    Alkyne metathesis is an organic reaction that entails the redistribution of alkyne chemical bonds. The reaction requires metal catalysts. Mechanistic studies show that the conversion proceeds via the intermediacy of metal alkylidyne complexes. [1] [2] The reaction is related to olefin metathesis .
    en.wikipedia.org/wiki/Alkyne_metathesis
    What is enyne metathesis?
    An Enyne metathesis is an organic reaction taking place between an alkyne and an alkene with a metal carbene catalyst forming a butadiene. This reaction is a variation of olefin metathesis.
    en.wikipedia.org/wiki/Enyne_metathesis
    What is Schrock's olefin metathesis?
    Schrock entered the olefin metathesis field in 1979 as an extension of work on tantalum alkylidenes. The initial result was disappointing as reaction of CpTa (=CH−t−Bu)Cl2 with ethylene yielded only a metallacyclopentane, not metathesis products:
    en.wikipedia.org/wiki/Olefin_metathesis
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    https://en.wikipedia.org/wiki/Olefin_metathesis

    Olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than … See more

    The reaction requires metal catalysts. Most commercially important processes employ heterogeneous catalysts. The heterogeneous catalysts are often prepared by in-situ activation of a metal halides (MClx) using See more

    Historical overview image
    Mechanism image

    Some important classes of olefin metathesis include:
    • Cross metathesis (CM)
    • Ring-opening metathesis (ROM) See more

    "Olefin metathesis is a child of industry and, as with many catalytic processes, it was discovered by accident." As part of ongoing work in what would later become known as Ziegler–Natta catalysis Karl Ziegler discovered the conversion of ethylene See more

    Overview image

    Olefin metathesis has several industrial applications. Almost all commercial applications employ heterogeneous catalysts using catalysts developed well before the Nobel-Prize winning work on homogeneous complexes. Representative processes include: See more

    Hérisson and Chauvin first proposed the widely accepted mechanism of transition metal alkene metathesis. The direct [2+2] cycloaddition of two alkenes is formally symmetry forbidden and thus has a high activation energy. The Chauvin mechanism … See more

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  4. https://en.wikipedia.org/wiki/Carbonyl_olefin_metathesis

    Carbonyl olefin metathesis is a type of metathesis reaction that entails, formally, the redistribution of fragments of an alkene and a carbonyl by the scission and regeneration of carbon-carbon and carbon-oxygen double bonds respectively. It is a powerful method in organic synthesis using simple carbonyls and olefins and converting them into less accessible products with higher structural complexity.

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    • https://en.wikipedia.org/wiki/Talk:Olefin_metathesis
      • I reorganized the article so the more basic, layman's information is first, followed by most of the technical jargon that would just drive off the average reader before they understand the significance of the reaction and why this particular bit of chemistry, among thousands of other discoveries, won a nobel prize. Duesling, calm down, eh? This is ...
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      • https://commons.wikimedia.org/wiki/Category:Olefin_metathesis

        WebMedia in category "Olefin metathesis" The following 76 files are in this category, out of 76 total. 1,2-Dihydro-1,2-azaborine synthesis (abbreviated).png 713 × 118; 8 KB

      • Olefin metathesis - Wikipedia

        https://wiki.alquds.edu/?query=Olefin_metathesis

        WebJul 09, 2022 · Olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double …

      • https://en.wikipedia.org/wiki/Ring-closing_metathesis

        WebRing-closing metathesis is a widely used variation of olefin metathesis in organic chemistry for the synthesis of various unsaturated rings via the intramolecular metathesis of two …

      • https://en.wikipedia.org/wiki/Alkyne_metathesis

        WebAlkyne metathesis is an organic reaction that entails the redistribution of alkyne chemical bonds. The reaction requires metal catalysts. Mechanistic studies show that the …

      • https://en.wikipedia.org/wiki/Ring-opening_metathesis_polymerisation

        WebRing-opening metathesis polymerization is a type of olefin metathesis chain-growth polymerization. The driving force of the reaction is relief of ring strain in cyclic olefins. A …

      • https://en.wikipedia.org/wiki/Enyne_metathesis

        WebAn enyne metathesis is an organic reaction taking place between an alkyne and an alkene with a metal carbene catalyst forming a butadiene. This reaction is a variation of olefin

      • https://www.wikipedia.org/wiki/Olefin_metathesis

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