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
- 1 January 1976
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 9,p. 330-331
- https://doi.org/10.1039/c39760000330
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.This publication has 1 reference indexed in Scilit:
- Postinfectional inhibitors from plants. XXIII. Sesquiterpenoid phytoalexins from fruit capsules of Datura stramoniumCanadian Journal of Botany, 1976