Ammonium Salt-Catalyzed Ring-Opening of Aryl-Aziridines with β-Keto Esters.

We herein report an ammonium salt-catalyzed protocol for the regioselective ring opening of aryl-aziridines with β-keto esters. The reaction gives access to a variety of highly functionalized target molecules with two consecutive stereo-genic centers and can be rendered enantioselective (up to = 91:9) by using bifunctional chiral ammonium salt catalysts.