Issue 3, 1981

Mode of enzymic oxygenation at primary carbon atoms: stereochemistry of hydroxylation of C-1 chiral octanes by Pseudomonas oleovorans

Abstract

It was shown, using (1R)- and (1S)-[1-3H,2H,1H;14C]octanes, that C-1 hydroxylatioin by P. oleovorans strain TF4-1L proceeds with retention of configuration.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 76-78

Mode of enzymic oxygenation at primary carbon atoms: stereochemistry of hydroxylation of C-1 chiral octanes by Pseudomonas oleovorans

E. Caspi, J. Piper and S. Shapiro, J. Chem. Soc., Chem. Commun., 1981, 76 DOI: 10.1039/C39810000076

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