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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. Miyaura borylation - Wikipedia

    en.wikipedia.org/wiki/Miyaura_borylation

    The Miyaura borylation has shown to work for: Alkyl halides, [ 2 ] aryl halides, [ 1 ] [ 3 ] [ 4 ] aryl halides using tetrahydroxydiboron , [ 5 ] aryl halides using bis-boronic acid, [ 6 ] aryl triflates , [ 7 ] aryl mesylates , [ 8 ] vinyl halides, [ 9 ] vinyl halides of α,β-unsaturated carbonyl compounds, [ 10 ] and vinyl triflates.

  5. Akira Suzuki - Wikipedia

    en.wikipedia.org/wiki/Akira_Suzuki

    Akira Suzuki (鈴木 章, Suzuki Akira, born September 12, 1930) is a Japanese chemist and Nobel Prize Laureate (2010), who first published the Suzuki reaction, the organic reaction of an aryl- or vinyl-boronic acid with an aryl- or vinyl-halide catalyzed by a palladium(0) complex, in 1979.

  6. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    The Sonogashira cross-coupling reaction has been employed in a wide variety of areas, due to its usefulness in the formation of carbon–carbon bonds. The reaction can be carried out under mild conditions, such as at room temperature, in aqueous media, and with a mild base, which has allowed for the use of the Sonogashira cross-coupling ...

  7. Decarboxylative cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Decarboxylative_cross-coupling

    Pd-catalyzed decarboxylative cross-coupling of aryl halides with potassium cyanoacetate, reported by Yeung et al. Contrarily to Cu-only systems, decarboxylative palladation is the rate-limiting step in the palladium catalytic cycle. [4] Decarboxylative cross-coupling of potassium polyfluorobenzoates, reported by Shang et al.

  8. Suzuki K engine - Wikipedia

    en.wikipedia.org/wiki/Suzuki_K_engine

    The Suzuki K engine family is a series of automobile engines from Suzuki, introduced in 1994. Displacements range from 0.7 L to 1.5 L. Displacements range from 0.7 L to 1.5 L. All engines have aluminium cylinder blocks with three or four cylinders in-line.

  9. Cross electrophile coupling - Wikipedia

    en.wikipedia.org/wiki/Cross_Electrophile_Coupling

    Cross electrophile coupling is a type of cross-coupling reaction that occurs between two electrophiles. It is often catalyzed by transition metal catalyst(s). Unlike conventional cross-coupling reactions of an electrophile with an organometallic reagent, [1] the coupling partners in cross electrophile coupling reactions are both electrophiles. [2]