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  2. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalysts. One important reaction type is this:

  3. 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 ...

  4. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    In one important reaction type, a main group organometallic compound of the type R-M (where R = organic group, M = main group centre metal atom) reacts with an organic halide of the type R'-X with formation of a new carbon-carbon bond in the product R-R'. The most common type of coupling reaction is the cross coupling reaction. [1] [2] [3]

  5. Living polymerization - Wikipedia

    en.wikipedia.org/wiki/Living_polymerization

    Chain termination and chain transfer reactions are absent and the rate of chain initiation is also much larger than the rate of chain propagation. The result is that the polymer chains grow at a more constant rate than seen in traditional chain polymerization and their lengths remain very similar (i.e. they have a very low polydispersity index).

  6. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    The Sonogashira reaction is a cross-coupling reaction used in organic synthesis to form carbon–carbon bonds. It employs a palladium catalyst as well as copper co-catalyst to form a carbon–carbon bond between a terminal alkyne and an aryl or vinyl halide .

  7. Kumada coupling - Wikipedia

    en.wikipedia.org/wiki/Kumada_coupling

    In organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carbon–carbon bonds by the reaction of a Grignard reagent and an organic halide. The procedure uses transition metal catalysts , typically nickel or palladium, to couple a combination of two alkyl , aryl or vinyl groups .

  8. Conjugated microporous polymer - Wikipedia

    en.wikipedia.org/wiki/Conjugated_microporous_polymer

    Building blocks that make up the network of CMPs must contain an aromatic system and have at least two reactive groups. To generate the porous structure of CMPs, cross-coupling of building blocks with different geometries to create a 3-D polymer backbone is necessary, while self-condensation reactions occur in the homo-coupling of building blocks with similar geometry. [2]

  9. Cross-coupling partner - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_partner

    In cross-coupling reactions, the component reagents are called cross-coupling partners or simply coupling partners. These reagents can be further classified according to their nucleophilic vs electrophilic character: R-X + R'-Y → R-R' + XY. Typically the electrophilic coupling partner (R-X) is an aryl halide, but triflates are also used ...