A Concise Enantioselective Synthesis of<i>N</i>-Boc-(<i>S</i>)-2-Aminosuberic Acid

Abstract

Abstract The title compound has been enantioselectively obtained by a four-step process involving the catalytic asymmetric epoxidation of allyl alcohol 3, regio- and stereoselective oxirane opening with benzhydrylamine and one-pot oxidative cleavage-amine reprotection.