24-nor-5β-chol-22-enes derived from the major bile acids by oxidative decarboxylation
- 1 December 1977
- Vol. 30 (6) , 787-793
- https://doi.org/10.1016/s0039-128x(77)80024-x
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Formylated bile acids: Improved synthesis, properties, and partial deformylationSteroids, 1977
- New bile alcohols — synthesis of 5β-cholestane-3α, 7α, 25-triol and 5β-cholestane-3α, 7α, 25-24(14C)-triol1Steroids, 1975
- Improved methods for the side-chain degradation of lanosterol. Synthesis of 4,4,14.alpha.-trimethyl-5.alpha.-pregn-8-en-20-one derivativesThe Journal of Organic Chemistry, 1974
- Steroids derived from bile acids. Novel side-chain degradation schemeThe Journal of Organic Chemistry, 1973
- Synthetic approaches to steroidal alkaloids II. Preparation and reactions of 12-oxo-dinorcholanic acidsSteroids, 1970
- SYNTHESES OF O, S-DICHOLANOYL-THIAMINE DERIVATIVESTHE JOURNAL OF VITAMINOLOGY, 1965
- Zur Kenntnis der Chenodesoxycholsäure (3α, 7α‐Dihydroxy‐5β‐cholansäure)Helvetica Chimica Acta, 1960
- Bile Acid Content of Human Serum. I. Serum Bile Acids in Patients with Hepatic Disease1Journal of Clinical Investigation, 1957
- THE CONVERSION OF HYODESOXYCHOLIC ACID TO PROGESTERONECanadian Journal of Chemistry, 1956
- STEROIDS. XXXVII.1 A TEN STEP CONVERSION OF PROGESTERONE TO CORTISONEJournal of the American Chemical Society, 1952