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Enantiocontrolled synthesis of alpha-methyl amino acids via Bn2N-alpha-methylserine-beta-lactone
Authors:Smith Nicole D  Wohlrab Aaron M  Goodman Murray
Affiliation:Department of Chemistry, University of California, San Diego, La Jolla, California 92093, USA. smithn@uchicago.edu
Abstract:[Reaction: see text] Enantiocontrolled synthesis of alpha-methyl amino acids proceeds via the regioselective organocuprate opening of Bn2N-alpha-methylserine-beta-lactone. From this chiral intermediate, a wide variety of alpha-methyl amino acids and building blocks were synthesized in excellent yields.
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