(+)-Occidentalol: Absolute Stereostructure and Total Synthesis
- 1 February 1972
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 50 (3) , 340-345
- https://doi.org/10.1139/v72-051
Abstract
Hydroxy ketone 7 has been prepared from both (+)-dihydrocarvone (3) and (+)-occidentalol (2), thus establishing the absolute stereostructure of the latter. The three-stage conversion of compound 7 into (+)-occidentalol constitutes a total synthesis of the sesquiterpene.Keywords
This publication has 0 references indexed in Scilit: