Issue 24, 1975

Stereochemistry of the glycine reductase of Clostridium sticklandii

Abstract

In the reductive deamination of glycine to acetic acid catalysed by glycine reductase of Clostridium sticklandii it is shown that both hydrogens are retained in the product and that the reaction proceeds with an inversion of configuration at the methylene carbon.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 980-982

Stereochemistry of the glycine reductase of Clostridium sticklandii

G. Barnard and M. Akhtar, J. Chem. Soc., Chem. Commun., 1975, 980 DOI: 10.1039/C39750000980

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