The preparation and biological activity of 9α,11β-dichloro-21-hydroxy-16α,17α-isopropylidenedioxypregna-1,4-diene-3,20-dione
- 1 March 1963
- Vol. 1 (3), 331-339
- https://doi.org/10.1016/s0039-128x(63)80116-6
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Comparison of Potency Estimates for Glucocorticoids Using Two Thymolytic Assay ProceduresExperimental Biology and Medicine, 1962
- 11-Alkylated Steroids. IV.1 Synthesis and Reactions of Olefins Derived from 11β-Hydroxy-11-methyl-5β-pregnane-3,20-dioneThe Journal of Organic Chemistry, 1962
- 17,21-Acetonide Derivatives of 9,11-Disubstituted Cortical HormonesThe Journal of Organic Chemistry, 1961
- BIOLOGICAL ACTIVITY OF 9α,llβ-DIHALO STEROIDS12Endocrinology, 1961
- 16-Hydroxylated Steroids. XII.1 The 16α,17α-Acetonides of Synthetic Non-halogenated Corticoids.Journal of the American Chemical Society, 1959
- A New Class of Potent Anti-inflammatory Agents; Synthesis of 9α,11β-DihalocorticosteroidsJournal of the American Chemical Society, 1959
- 16-Hydroxylated Steroids. VI1 The Synthesis of the 16α-Hydroxy Derivatives of 9α-Substituted SteroidsJournal of the American Chemical Society, 1959
- CYCLIC 16α,17α-KETALS AND ACETALS OF 9α-FLUORO-16α-HYDROXY-CORTISOL AND -PREDNISOLONEJournal of the American Chemical Society, 1958
- Synthetic Derivatives of Cortical HormonesPublished by Elsevier ,1958