An efficient method for converting 17-oxo- into 17-acetyl steroids
- 1 January 1975
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 31 (17) , 2151-2155
- https://doi.org/10.1016/0040-4020(75)80211-0
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Synthesis of Stereochemistry of 4-ethoxy-2-oxazolinesTetrahedron Letters, 1974
- A synthetic method for direct conversion of ketones into cyanides. Introduction of a one carbon unit.Tetrahedron Letters, 1973
- Vanadium (IV) chloride induced allylic rearrangement of a steroidal alcoholSteroids, 1972
- A novel and efficient synthesis of oxazoles from tosylmethylisocyanide and carbonyl compoundsTetrahedron Letters, 1972
- A Simple One-Step Synthesis of 2-Cyanoadamantane, a Precursor to Adamantane-2-Carboxylic AcidSynthetic Communications, 1972
- A two-step synthesis of the pregnane and corticoid side-chainsJournal of the Chemical Society D: Chemical Communications, 1971
- 11-Alkylated steroids. VI. 11.beta.-hydroxy-11.alpha.-methyl-5.beta.-pregnan-20-oneJournal of Medicinal Chemistry, 1968
- Spectra and Stereochemistry. VII.1,2 Long-Range Shielding by Nitrile GroupsJournal of the American Chemical Society, 1963
- Steroids. XII.1 Aromatization Experiments in the Progesterone Series2Journal of the American Chemical Society, 1951