Issue 12, 1985

Oxytetracycline biosynthesis: mode of incorporation of [1-13C,18O2]acetate

Abstract

The regiospecific locations of [18O2]acetate-derived oxygen substituents of oxytetracycline (1) have been determined using the 13C n.m.r. isotope shift technique and shown to correspond exclusively to those oxygen-bearing carbons which originate biosynthetically from the carboxy group of acetate.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 802-803

Oxytetracycline biosynthesis: mode of incorporation of [1-13C,18O2]acetate

R. Thomas and D. J. Williams, J. Chem. Soc., Chem. Commun., 1985, 802 DOI: 10.1039/C39850000802

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