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  2. Ethenolysis - Wikipedia

    en.wikipedia.org/wiki/Ethenolysis

    In organic chemistry, ethenolysis is a chemical process in which internal olefins are degraded using ethylene (H 2 C=CH 2) as the reagent. The reaction is an example of cross metathesis . The utility of the reaction is driven by the low cost of ethylene as a reagent and its selectivity.

  3. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    In organic chemistry, 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. [ 1 ] [ 2 ] Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative ...

  4. Salt metathesis reaction - Wikipedia

    en.wikipedia.org/wiki/Salt_metathesis_reaction

    Salt metathesis is a common technique for exchanging counterions. The choice of reactants is guided by a solubility chart or lattice energy. HSAB theory can also be used to predict the products of a metathesis reaction. Salt metathesis is often employed to obtain salts that are soluble in organic solvents.

  5. Alkane metathesis - Wikipedia

    en.wikipedia.org/wiki/Alkane_metathesis

    Alkane metathesis is a class of chemical reaction in which an alkane is rearranged to give a longer or shorter alkane product. It is similar to olefin metathesis , except that olefin metathesis cleaves and recreates a carbon-carbon double bond, but alkane metathesis operates on a carbon-carbon single bond.

  6. Enyne metathesis - Wikipedia

    en.wikipedia.org/wiki/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. [1] The general scheme is given by scheme 1: When the reaction is intramolecular (in an enyne) it is called ring-closing enyne metathesis or RCEYM (scheme 2):

  7. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Often cross-coupling reactions require metal catalysts. One important reaction type is this: One important reaction type is this: R−M + R'−X → R−R' + MX (R, R' = organic fragments, usually aryl ; M = main group center such as Li or MgX; X = halide )

  8. Ring-opening metathesis polymerisation - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_metathesis...

    In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. [1] The reaction is driven by relieving ring strain in cyclic olefins. [2] A variety of heterogeneous and homogeneous catalysts have been developed for different polymers and mechanisms. [3]

  9. Carbonyl olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_olefin_metathesis

    The metal-mediated processes include a carbonyl-olefination and an olefin–olefin metathesis event. There are two general mechanistic schemes to perform this overall transformation: one, reaction of a [M=CHR 1] reagent with an alkene to generate a new metal alkylidene, which then couples with a carbonyl group to form the desired substituted alkene and an inactive [M=O] species (type A); two ...

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