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]](https://www.rsc.org/images/entities/char_e006.gif)
O →–CH2NH2.
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Article information
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J. Chem. Soc., Chem. Commun., 1983, 18-20
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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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