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  2. 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 ...

  3. Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Heck_reaction

    Heck was awarded the 2010 Nobel Prize in Chemistry, which he shared with Ei-ichi Negishi and Akira Suzuki, for the discovery and development of this reaction. This reaction was the first example of a carbon-carbon bond-forming reaction that followed a Pd(0)/Pd(II) catalytic cycle, the same catalytic cycle that is seen in other Pd(0)-catalyzed ...

  4. Heterogeneous metal catalyzed cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_metal...

    A 2021 survey of heterogeneous metal catalyzed cross-couplings in the fine chemical industry reported, out of 22 examples, 19 Suzuki or Heck reactions, which included only 2 examples with N-basic heterocycles, and only 4 examples with a singly-ortho-substituted electrophile (representative example in Scheme 1). [1]

  5. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Often cross-coupling reactions require metal catalysts. 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) These reactions are used to form carbon–carbon bonds but also carbon-heteroatom bonds.

  6. Intramolecular Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_Heck_reaction

    The Heck reaction is the palladium-catalyzed coupling of an aryl or alkenyl halide with an alkene to form a substituted alkene. [2] Intramolecular variants of the reaction may be used to generate cyclic products containing endo or exo double bonds. Ring sizes produced by the intramolecular Heck reaction range from four to twenty-seven atoms.

  7. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    The most common type of coupling reaction is the cross coupling reaction. [1] [2] [3] Richard F. Heck, Ei-ichi Negishi, and Akira Suzuki were awarded the 2010 Nobel Prize in Chemistry for developing palladium-catalyzed cross coupling reactions. [4] [5] Broadly speaking, two types of coupling reactions are recognized:

  8. Decarboxylative cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Decarboxylative_cross-coupling

    The most typical class of reactions involves coupling between C–COOH and C–X bonds, however C–COOH and C–M cross-coupling, homo-coupling of carboxylic acids, heck coupling, and dehydrogenative cross-coupling can also be including in this class as they release CO 2. Heteroatom cross coupling reactions involving formation of C–N, C–S ...

  9. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    Among the cross-coupling reactions it follows in the number of publications right after Suzuki and Heck reaction [8] and a search for the term "Sonogashira" in SciFinder provides over 1500 references for journal publications between 2007 and 2010. [7]