Chemical Communications · 2011 · 86 citations · 25 references
Chemical EngineeringCross-coupling ReactionAryl ChloridesSuzuki-miyaura Cross CouplingEngineeringHeterocyclicPalladium ComplexesOrganic ChemistryLiving CatalystOrganometallic CatalysisCatalysisChemistryCatalytic SynthesisSuzuki–miyaura Cross Coupling
Palladium complexes bearing abnormal N-heterocyclic carbene were used as catalysts in Suzuki-Miyaura cross coupling of aryl chlorides at 25 °C. The catalyst remained active for 10 successive catalytic runs and can activate 4-chlorotoluene at 25 °C with 0.01 mol% catalyst loading resulting in a TON of 9500 within 6 h.
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Ab initio molecular orbital theory
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Electronic stabilization of nucleophilic carbenes
Anthony J. Arduengo, H. V. Rasika Dias, Richard L. Harlow et al. · Journal of the American Chemical Society · 1992 · 1.1K citations
Nicolas Marion, Oscar Navarro, Jianguo Mei et al. · Journal of the American Chemical Society · 2006 · 895 citations
Inorganic Chemistry, Chemical Engineering, Room-temperature Suzuki−miyaura +14
Christopher J. O’Brien, Eric Assen B. Kantchev, Cory Valente et al. · Chemistry - A European Journal · 2006 · 810 citations