Issue 9, 1976

Sesquiterpenoid stress compounds of Datura stramonium: biosynthesis of the three major metabolites from [1,2-13C]acetate and the X-ray structure of 3-hydroxylubimin

Abstract

2,3-Germacrenediol, lubimin, and hydroxylubimin, the major stress metabolites of Datura stramonium, incorporate sodium [1,2-13C]acetate in patterns, as shown by 13C n.m.r. spectroscopy, which establish their structures and mevalonate origins; the X-ray structure of hydroxylubimin completely defines its stereochemistry.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 330-331

Sesquiterpenoid stress compounds of Datura stramonium: biosynthesis of the three major metabolites from [1,2-13C]acetate and the X-ray structure of 3-hydroxylubimin

G. I. Birnbaum, C. P. Huber, M. L. Post, J. B. Stothers, J. R. Robinson, A. Stoessl and E. W. B. Ward, J. Chem. Soc., Chem. Commun., 1976, 330 DOI: 10.1039/C39760000330

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