Abstract
Three palladium complexes derived from diphenyl-2-pyridylphosphine (PPh2Py) were investigated for their utility as catalysts for the Suzuki-Miyaura reactions of aryl halides in environment friendly solvents such as water, alcohols etc. Good-to-excellent yields of coupling products were achieved with a wide range of aryl halides under mild reaction conditions.
Keywords: Aqueous condition, diphenyl-2-pyridylphosphine, hemilabile ligand, palladium catalyst, room temperature, suzuki-miyaura reaction, biphenyl-type phosphine, phosphapalladacycles, bidentate phosphine, arylboronic, P-monodentate
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