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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. Norio Miyaura - Wikipedia

    en.wikipedia.org/wiki/Norio_Miyaura

    Norio Miyaura (宮浦憲夫, Miyaura Norio) was a Japanese organic chemist. He was a professor of graduate chemical engineering at Hokkaido University. [1] His major accomplishments surrounded his work in cross-coupling reactions / conjugate addition reactions of organoboronic acids (for C-C bond-forming reactions) and addition / coupling reactions of diborons and boranes (to synthesize ...

  4. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    Protodeboronation is a well-known undesired side reaction, and frequently associated with metal-catalysed coupling reactions that utilise boronic acids (see Suzuki reaction). [1] For a given boronic acid, the propensity to undergo protodeboronation is highly variable and dependent on various factors, such as the reaction conditions employed and ...

  5. Miyaura borylation - Wikipedia

    en.wikipedia.org/wiki/Miyaura_borylation

    Miyaura borylation, also ... of boronates from vinyl or aryl halides with the cross-coupling of ... can be used as coupling partners for the Suzuki reaction. [1]

  6. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    Then A. Suzuki and co-workers extend this kind of reaction to other organoboron compounds and other alkenyl, aryl, alkyl halides and triflate. The palladium-catalyzed cross-coupling reaction organoboron compounds and these organic halides to form carbon-carbon bonds are known as Suzuki–Miyaura cross-coupling. [41] [42] Suzuki-Miyaura Cross ...

  7. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Many mechanisms exist reflecting the myriad types of cross-couplings, including those that do not require metal catalysts. [7] Often, however, cross-coupling refers to a metal-catalyzed reaction of a nucleophilic partner with an electrophilic partner. Mechanism proposed for Kumada coupling (L = Ligand, Ar = Aryl).

  8. What’s closed on national day of mourning for Jimmy Carter

    www.aol.com/closed-national-day-mourning-jimmy...

    The US will honor the late former President Jimmy Carter, who died at age 100 on December 29. President Joe Biden declared January 9 as a day of mourning in an executive order – the same day as ...

  9. Palladium compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium_compounds

    General scheme of the Suzuki reaction Mechanism of the Suzuki reaction. Both ionic and coordination palladium compounds are frequently used to catalyze cross-coupling reactions. The catalytic ability is due to palladium's ability to switch between the Pd 0 and Pd 2+ oxidation states.