STEROID BIOSYNTHESIS. THE ABSOLUTE CONFIGURATION OF THE ENZYMATICALLY ACTIVE ENANTIOMER OF 2,3-OXIDOSQUALENE PARTICIPATING IN ITS CYCLIZATION TO LANOSTEROL
- 5 October 1973
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 2 (10) , 1137-1138
- https://doi.org/10.1246/cl.1973.1137
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Simple method for determining the chirality of cyclic .alpha.-glycols with Pr(DPM)3 and Eu(DPM)3Journal of the American Chemical Society, 1971
- Studies in phytosterol biosynthesis. Mechanism of biosynthesis of cycloartenolBiochemical Journal, 1968
- Enzymic Conversion of Squalene 2,3-Oxide to Lanosterol and CholesterolJournal of the American Chemical Society, 1966
- 2,3-Oxidosqualene, an Intermediate in the Biological Synthesis of Sterols from Squalene1Journal of the American Chemical Society, 1966