The Total Synthesis of Hydroxyisochamaecynone and Its Stereochemical Assignment
- 1 April 1980
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 53 (4) , 1039-1044
- https://doi.org/10.1246/bcsj.53.1039
Abstract
The structure of an acetylenic nor-sesquiterpene, hydroxyisochamaecynone, was determined to be 4α-hydroxy-5βH-13-noreudesm-1-en-11-yn-3-one (Ib) by means of the stereoselective total syntheses of two possible stereoisomers, Ib and 4β-hydroxy-5βH-13-noreudesm-1-en-11-yn-3-one.This publication has 4 references indexed in Scilit:
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