Electrocatalytic Allylic C−H Alkylation Enabled by a Dual‐Function Cobalt Catalyst**

Abstract

The direct functionalization of allylic CÀ H bonds with nucleophiles minimizes pre-functionalization and converts inexpensive, abundantly available materials to value-added alkenyl-substituted products but remains challenging. Here we report an electrocatalytic allylic CÀ H alkylation reaction with carbon nucleophiles employing an easily available cobalt-salen complex as the molecular catalyst. These C(sp 3 )À H/C(sp 3 )À H crosscoupling reactions proceed through H 2 evolution and require no external chemical oxidants. Importantly, the mild conditions and unique electrocatalytic radical process ensure excellent functional group tolerance and substrate compatibility with both linear and branched terminal alkenes. The synthetic utility of the electrochemical method is highlighted by its scalability (up to 200 mmol scale) under low loading of electrolyte (down to 0.05 equiv) and its successful application in the latestage functionalization of complex structures.