Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones
- 1 January 1977
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 1,p. 27-28
- https://doi.org/10.1039/c39770000027
Abstract
The structure and absolute stereochemistry of four new vetispirane sesquiterpene glucosides from fluecured Virginia tobacco have been deduced and three of them have been synthesised from (–)-solavetivone; the X-ray structure of the p-bromobenzenesulphonate of one of the derived aglycones is reported.This publication has 3 references indexed in Scilit:
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- Sesquiterpenoid stress compounds of Datura stramonium: biosynthesis of the three major metabolites from [1,2-13C]acetate and the X-ray structure of 3-hydroxylubiminJournal of the Chemical Society, Chemical Communications, 1976
- Tobacco Chemistry. 37. The Absolute Configuration of Prenylsolanone, (9S)-6,12-Dimethyl-9-isopropyltrideca-5E,10E,12-trien-2-one, a Northunberganoid of Nicotiana tabacum L..Acta Chemica Scandinavica, 1976