Issue 1, 1983

Mechanism and stereochemistry of the elaboration of the neosamine C ring in the biosynthesis of neomycins

Abstract

The amino-methyl group of the neosamine C ring of neomycins is formed by an oxidation–transamination process, –Ch2–OH →–CH[double bond, length half m-dash]O →–CH2NH2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 18-20

Mechanism and stereochemistry of the elaboration of the neosamine C ring in the biosynthesis of neomycins

W. Al-Feel, M. J. S. Ewad, C. J. Herbert and M. Akhtar, J. Chem. Soc., Chem. Commun., 1983, 18 DOI: 10.1039/C39830000018

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