Issue 5, 1991

Asymmetric induction in radical reactions: enantioselective syntheses of (S)-2-deuterioglycine and (R)-2-deuterioglycine

Abstract

The (–)-8-phenylmenthol ester of N-Boc-glycine is brominated with N-bromosuccinimide and the bromo-compound is reduced with tri-n-butyldeuteriostannane to give the chiral glycine derivative in high optical yield which upon hydrolysis yields the amino acid without racemisation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 332-333

Asymmetric induction in radical reactions: enantioselective syntheses of (S)-2-deuterioglycine and (R)-2-deuterioglycine

D. P. G. Hamon, P. Razzino and R. A. Massy-Westropp, J. Chem. Soc., Chem. Commun., 1991, 332 DOI: 10.1039/C39910000332

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