A Concise Enantioselective Synthesis ofN-Boc-(S)-2-Aminosuberic Acid

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.

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