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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. 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 ...

  4. Organotrifluoroborate - Wikipedia

    en.wikipedia.org/wiki/Organotrifluoroborate

    The mechanism of organotrifluoroborate-based Suzuki-Miyaura coupling reactions has recently been investigated in detail. The organotrifluoroborate hydrolyses to the corresponding boronic acid in situ , so a boronic acid can be used in place of an organotrifluoroborate, as long as it is added slowly and carefully.

  5. 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:

  6. Transition metal pincer complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_pincer...

    The general mechanism for the Suzuki reaction. Pincer complexes have been shown to catalyse Suzuki-Miyaura coupling reactions, a versatile carbon-carbon bond forming reaction. Typical Suzuki coupling employ Pd(0) catalysts with monodentate tertiary phosphine ligands (e.g. Pd(PPh 3) 4). It is a very selective method to couple aryl substituents ...

  7. Mortgage and refinance rates for Jan. 6, 2025: Average rates ...

    www.aol.com/finance/mortgage-and-refinance-rates...

    The unemployment rate edged up moderately to 4.2% from October's 4.1%. A new labor reading for December is due on January 10, 2025 — the first major economic report in the new year.

  8. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Cross-coupling reactions are important for the production of pharmaceuticals, [4] examples being montelukast, eletriptan, naproxen, varenicline, and resveratrol. [21] with Suzuki coupling being most widely used. [22] Some polymers and monomers are also prepared in this way. [23]

  9. Macy’s is in deep trouble. It could be sitting on a gold mine

    www.aol.com/finance/macy-deep-trouble-could...

    The investors claim that Macy’s real estate, including its flagship store at Herald Square in New York City, is worth up to $9 billion on the open market, nearly double Macy’s closing market ...