Remote Site-Selective Asymmetric Protoboration of Unactivated Alkenes Enabled by Bimetallic Relay Catalysis

A remote C(sp(3))-H bond asymmetric borylation of unactivated alkenes was achieved by bimetallic relay catalysis. The reaction proceeded through reversible and consecutive beta-H elimination/olefin insertion promoted by CoH species generated in situ, followed by copper-catalyzed asymmetric protoboration. The use of this synergistic Co/Cu catalysis protocol allowed the enantioselective protoboration of various unactivated terminal alkenes and internal alkenes, as well as an unrefined mixture of olefin isomers, at the distal less-reactive beta-position to a functional group, leading to chiral organoboronates.

Automated summary

The remote C(sp(3))-H bond asymmetric borylation of unactivated alkenes was successfully achieved by bimetallic relay catalysis, allowing the efficient synthesis of chiral organoboronates.