Dirhodium(II)/Phosphine Catalyst with Chiral Environment at Bridging Site and Its Application in Enantioselective Atropisomer Synthesis

A dirhodium(II)/phosphine catalyst with a chiral environment at the bridging site was developed for the asymmetric arylation of phenanthrene-9,10-diones with arylboronic acids. In contrast to the classic chiral bridging carboxylic acid (or derivatives) ligand strategy of bimetallic dirhodium(II) catalysis, in this reaction, tuning both axial and bridging ligands realized the first Rh2(OAc)4/phosphine-catalyzed highly enantioselective carbonyl addition reaction. The kinetic analysis reveals that dirhodium(II) and arylboronic acid follow the first-order kinetics, while phenanthrene-9,10-dione is zeroth-order. These data supported the proposed catalytic cycle, where the key intermediate in the rate-determining step involved the dirhodium(II) complex and arylboronic acid. Finally, axially chiral biaryls were prepared based on a newly developed oxidative ring-opening reaction of alpha hydroxyl ketones with a base and molecular oxygen, which featured a central-to-axial chirality transfer radical beta-scission step.

Automated summary

A dirhodium(II)/phosphine catalyst was developed for the asymmetric arylation of phenanthrene-9,10-diones with arylboronic acids. The chiral environment at the bridging site and tuning of axial and bridging ligands enabled highly enantioselective carbonyl addition reaction. Kinetic analysis showed that the rate-determining step involved the dirhodium(II) complex and arylboronic acid. Axially chiral biaryls were prepared through an oxidative ring-opening reaction.