Nickel-Catalyzed Ligand-Controlled Regioselective Allylic Alkenylation of Allylic Alcohols with Easily Accessible Alkenyl Boronates: Synthesis of 1,4-Dienes.

A nickel-catalyzed direct reaction of allylic alcohols with easily accessible alkenyl boronates has been developed, which provides valuable 1,4-dienes with high regio- and stereoselectivity in good to excellent yields, wide substrate scope, and functional group compatibility. The catalytic system simply consists of Ni(cod) 2 as the catalyst and a ligand, without a need for a base and alcohol activator in most cases. The proper choice of ancillary ligands is highly important for this reaction. Depending on the substitution pattern of allylic alcohols and/or alkenyl boronates, different ligands were used for improving the reaction efficiency.