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  2. 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 ...

  3. 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.

  4. Process chemistry - Wikipedia

    en.wikipedia.org/wiki/Process_chemistry

    Process chemistry is the arm of pharmaceutical chemistry concerned with the development and ... For the unoptimized cross-metathesis reaction using the Grela catalyst ...

  5. 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 ...

  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. Concurrent tandem catalysis - Wikipedia

    en.wikipedia.org/wiki/Concurrent_tandem_catalysis

    Cossy et al. report a simple synthesis to form substituted five and six membered lactones from the cross metathesis of an allylic or homoallylic alcohol and acrylic acid using a ruthenium based metathesis catalyst.

  8. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  9. Salt metathesis reaction - Wikipedia

    en.wikipedia.org/wiki/Salt_metathesis_reaction

    A salt metathesis reaction is a chemical process involving the exchange of bonds between two reacting chemical species which results in the creation of products with similar or identical bonding affiliations. [1] This reaction is represented by the general scheme: + +