Enantioselective Rh-Catalyzed Hydroboration of Silyl Enol Ethers

The asymmetric hydroboration of alkenes has proven to be among the most powerful methods for the synthesis of chiral boron compounds. This protocol is well suitable for activated alkenes such as vinylarenes and alkenes bearing directing groups. However, the catalytic enantioselective hydroboration of 0-substituted alkenes has remained unprecedented. Here we report a R-hcatalyzed enantioselective hydroboration of silyl enol ethers (SEEs) that utilizes two new chiral phosphine ligands we developed. This approach features mild reaction conditions and a broad substrate scope as well as excellent functional group tolerance, and enables highly efficient preparation of synthetically valuable chiral borylethers.

Automated summary

Researchers reported a catalytic enantioselective hydroboration of silyl enol ethers (SEEs) using two new chiral phosphine ligands, featuring mild reaction conditions and a broad substrate scope.