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Title: Palladium- and nickel-catalyzed Kumada cross-coupling reactions of gem-difluoroalkenes and monofluoroalkenes with Grignard reagents. Author: Dai W, Xiao J, Jin G, Wu J, Cao S. Journal: J Org Chem; 2014 Nov 07; 79(21):10537-46. PubMed ID: 25327183. Abstract: A novel Kumada-Tamao-Corriu cross-coupling reaction of gem-di- or monofluoroalkenes with Grignard reagents, with or without β-hydrogen atoms, in the presence of a catalytic amount of palladium- or nickel-based catalysts has been developed. The reaction is performed under mild conditions (room temperature or reflux in diethyl ether for 1-2 h) and leads to di-cross- or mono-cross-coupled products in good to high yields.[Abstract] [Full Text] [Related] [New Search]