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  2. Intramolecular Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_Heck_reaction

    Intramolecular Heck reactions have been employed for the construction of complex natural products. An example is the late-stage, macrocyclic ring closure in the total synthesis of the cytotoxic natural product (–)-Mandelalide A. [19] In another example a fully intramolecular tandem Heck reaction is used in a synthesis of (–)-scopadulcic acid.

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  4. Richard F. Heck - Wikipedia

    en.wikipedia.org/wiki/Richard_F._Heck

    Richard Frederick Heck (August 15, 1931 – October 9, 2015) was an American chemist noted for the discovery and development of the Heck reaction, which uses palladium to catalyze organic chemical reactions that couple aryl halides with alkenes. The analgesic naproxen is an example of a compound that is prepared industrially using the Heck ...

  5. Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Heck_reaction

    The Heck reaction (also called the Mizoroki–Heck reaction) [1] is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst to form a substituted alkene. It is named after Tsutomu Mizoroki and Richard F. Heck.

  6. Category:Carbon-carbon bond forming reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Carbon-carbon...

    Hammick reaction; Heck reaction; Henry reaction; Heterogeneous metal catalyzed cross-coupling; High dilution principle; Hiyama coupling; Homologation reaction; Horner–Wadsworth–Emmons reaction; Hydrocyanation; Hydrovinylation; Hydroxymethylation

  7. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    The reaction is named after Ei-ichi Negishi who was a co-recipient of the 2010 Nobel Prize in Chemistry for the discovery and development of this reaction. Negishi and coworkers originally investigated the cross-coupling of organoaluminum reagents in 1976 initially employing Ni and Pd as the transition metal catalysts, but noted that Ni ...

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