NMR Study of Some Sesquiterpene Alcohols and Their Oxidation Products
Authors:
- 1 March 1974
- journal article
- research article
- Published by Wiley in Journal of the Chinese Chemical Society
- Vol. 21 (1) , 31-35
Abstract
Oxidations of α‐cadinol, T‐cadinol, T‐muurolol and δ‐cadinol with SeO3 gave corresponding ketols and diols. Reductions of the ketols with NaBH4 gave epidiols. NMR data of these sixteen compounds are compared.Keywords
This publication has 3 references indexed in Scilit:
- The structure of δ-cadinol—amorphan-3-ene-9β-olTetrahedron, 1971
- The Oxymercuration-Demercuration of Representative Olefins. A Convenient, Mild Procedure for the Markovnikov Hydration of the Carbon-Carbon Double BondJournal of the American Chemical Society, 1967
- Some Observations on Allylic Oxidation1The Journal of Organic Chemistry, 1964