Catalytic Asymmetric Reductive Azaarylation of Olefins via Enantioselective Radical Coupling.

Visible-light-driven photocatalytic reductive azaarylation has been widely used to construct the important imine-containing azaarene derivatives. In addition to the direct use of various commercially available cyanoazaarenes as feedstocks, the synthetic advantages include precise regioselectivity, high efficiency, mild reaction conditions, and good functional group tolerance. However, although many efficient reductive azaarylation methods have been established, the example of an enantioselective manner is still unmet, which most likely can be ascribed to the highly reactive radical coupling as the key step of forming stereocenters. Exploring the feasibility of enantiocontrol thus constitutes an attractive but highly challenging task. Here, we demonstrate that chiral hydrogen-bonding/photosensitizer catalysis is a viable platform as it enables the realization of the first enantioselective manifold. A variety of acyclic and cyclic enones as the reaction partners are compatible with the dual catalyst system, leading to a wide array of valuable enantioenriched azaarene variants with high yields and ees. Regulating the types of chiral catalysts represents one of the important manners to success, in which several readily accessible Cinchona alkaloid-derived bifunctional catalysts are introduced in asymmetric photochemical reactions.