Lewis Base/Copper Cooperatively Catalyzed Asymmetric α‑Amination of Esters with Diaziridinone

An enantioselective α-amination of esters by a Lewis base/copper­(I) cooperative catalysis strategy has been developed. The transient chiral C1-ammonium enolate generated from pentafluorophenyl ester and nucleophilic Lewis base is nicely compatible with the copper intermediate formed from N,N-di-t-butyldiaziridinone and Cu­(I) to allow for high levels of stereochemical control. The cooperative catalytic reaction leads to a diverse set of highly enantioenriched hydantoins in good yields with excellent enantioselectivities (90–99% ee).