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- https://chem.libretexts.org/Bookshelves/Inorganic_Chemistry/Supplemental_Modules_and_Websites_(Inorganic_Chemistry)/Catalysis/Catalyst_Examples/Suzuki-Miyaura_CouplingSuzuki-Miyaura coupling (or Suzuki coupling) is a metal catalyzed reaction, typically with Pd, between an alkenyl (vinyl), aryl, or alkynyl organoborane (boronic acid or boronic ester, or special case...Suzuki-Miyaura coupling (or Suzuki coupling) is a metal catalyzed reaction, typically with Pd, between an alkenyl (vinyl), aryl, or alkynyl organoborane (boronic acid or boronic ester, or special cases with aryl trifluoroborane) and halide or triflate under basic conditions. This reaction is used to create carbon-carbon bonds to produce conjugated systems of alkenes, styrenes, or biaryl compounds.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/10%3A_Organohalides/10.07%3A_Organometallic_Coupling_ReactionsA detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copp...A detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copper in the Gilman reagent being oxidized from Cu +1 to Cu +3 . Losing electrons allows the copper atom to act as a nucleophile and undergo an S N 2 like substitution reaction with the alkyl halide.
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/10%3A_Organohalides/10.08%3A_Organometallic_Coupling_ReactionsA detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copp...A detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copper in the Gilman reagent being oxidized from Cu +1 to Cu +3 . Losing electrons allows the copper atom to act as a nucleophile and undergo an S N 2 like substitution reaction with the alkyl halide.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/10%3A_Organohalides/10.07%3A_Organometallic_Coupling_ReactionsA detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copp...A detailed discussion of these modifications is beyond the scope of this course, but you should be aware of possible limitations in the use of the Corey-House synthesis. The mechanism begins with copper in the Gilman reagent being oxidized from Cu +1 to Cu +3 . Losing electrons allows the copper atom to act as a nucleophile and undergo an S N 2 like substitution reaction with the alkyl halide.
