Electrochemical-Promoted Nickel-Catalyzed Reductive Allylation of Aryl Halides

Compared with conventional reductive coupling, reductive coupling under electrochemical conditions without external reductants is greener, milder, and more efficient and is of increasing interest to organic chemists. In this work, we report the sacrificial anode, nickel-catalyzed electrochemical allylation reaction of aryl and alkyl halides. The reaction can be applied to a range of allylation reagents such as trifluoroalkenes, oxalates, and acetates.