The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine (Beilstein Journal of Organic Chemistry)

Abstract A simple enantioselective synthetic procedure for the preparation of mianserin and epinastine in optically pure form is described. The key step in the synthetic pathway is the asymmetric reduction of the cyclic imine using asymmetric transfer hydrogenation conditions. Beilstein J. Org. Chem. 2015, 11, 1509–1513. doi:10.3762/bjoc.11.164