A simple route to steroid 17α,20α,21-triols and their 21-monoesters
- 1 January 1965
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 21 (1) , 179-191
- https://doi.org/10.1016/s0040-4020(01)82212-2
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Structure and the Optical Rotatory Dispersion of Saturated KetonesJournal of the American Chemical Society, 1961
- 17α,21-ISOPROPYLIDENEDIOXY STEROIDSJournal of the American Chemical Society, 1961
- Selective Sodium Borohydride Reductions in Aqueous Dimethylformamide Solution. Neighboring Group Effects in the Cortical Side Chain1Journal of the American Chemical Society, 1959
- The Stereochemistry of the Hydride Reduction of Some Steroidal KetonesJournal of the American Chemical Society, 1956
- The Stereochemistry of Hydride ReductionsJournal of the American Chemical Society, 1956
- 11-Oxygenated Steroids. IV. The Selective Reduction of Steroidal 11,20-Diketones with Sodium Borohydride1Journal of the American Chemical Society, 1953
- Synthesis of 11-Hydroxylated Cortical Steroids. The Preferential Reduction of Carbonyl Systems in the Presence of Carbon—Nitrogen Multiple BondsJournal of the American Chemical Society, 1951
- Sterols. XII. The Partial Synthesis of 4-Pregnene-17α,20,21-triol-3-ones and Reichstein's Substance E1Journal of the American Chemical Society, 1951
- Partial Synthesis of Reichstein's Substance E1Journal of the American Chemical Society, 1951
- Stereoisomeric Substituted 11-Keto-20-hydroxypregnanes. IIJournal of the American Chemical Society, 1949