Asymmetric Allylic Amination of Morita–Baylis–Hillman Carbonates with Silylated <i>tert</i>‐Butylhydroxycarbamate Derivatives

Abstract

The enantioselective amination of Morita–Baylis–Hillman carbonates with silylated derivatives of tert ‐butylhydroxycarbamates using β‐isocupreidine as an organocatalyst was investigated. The corresponding products were obtained in good yields with high enantioselectivities. The scope and limitations of the reported protocol were explored, and representative transformations of the adducts toward heterocyclic compounds were highlighted.