Issue 9, 1976

Pattern of acetate incorporation into the aglycone of chartreusin. Evidence from 13C nuclear magnetic resonance studies for a single-chain polyketide intermediate

Abstract

13 C N.m.r. analysis of the labelling pattern in chartreusin biosynthesized from singly and doubly 13C- labelled acetate has indicated that the aglycone is formed by condensation and subsequent scission of a single polyketide chain of 22 carbon atoms.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 319-320

Pattern of acetate incorporation into the aglycone of chartreusin. Evidence from 13C nuclear magnetic resonance studies for a single-chain polyketide intermediate

P. Canham and L. C. Vining, J. Chem. Soc., Chem. Commun., 1976, 319 DOI: 10.1039/C39760000319

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