The biosynthesis of 23,24-dinor-5-cholene-3β,20-diol and 23,24-dinor-5-cholene-3β, 21-diol
- 31 August 1973
- Vol. 22 (2) , 239-245
- https://doi.org/10.1016/0039-128x(73)90088-3
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- The conversion of 23,24-dinor-chol-5-en-3β-ol into steroid hormonesBiochemical Journal, 1972
- Biochemical conversion of partially cyclized squalene 2,3-oxide types to the lanosterol system. Views on the normal enzymic cyclization processJournal of the American Chemical Society, 1970
- Enzymic transformation of an acyclic sesterterpene terminal epoxide into a lanosterol analogueJournal of the Chemical Society D: Chemical Communications, 1969
- A Preparation of 3β-Hydroxypregn-5-en-20-one-4-C14The Journal of Organic Chemistry, 1958
- Synthesis of Steroidal Methylene Compounds by the Wittig Reaction1Journal of the American Chemical Society, 1957