Regioselective synthesis of a-ring halogenated derivatives of 17α-ethynyloestradiol
- 1 January 1991
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 47 (16-17) , 2871-2878
- https://doi.org/10.1016/s0040-4020(01)87092-7
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Efficient regioselective a-ring functionalization of oestrogensTetrahedron, 1990
- 2-bromo- and 16-bromo-estrogens and related compounds: Potential inhibitors for both estradiol 2- and 16α-hydroxylases in rat liver microsomesThe Journal of Steroid Biochemistry and Molecular Biology, 1989
- Drug protein conjugates—III. Inhibition of the irreversible binding of ethinylestradiol to rat liver microsomal protein by mixed-function oxidase inhibitors, ascorbic acid and thiolsThe Journal of Steroid Biochemistry and Molecular Biology, 1983
- Drug-protein conjugates—VBiochemical Pharmacology, 1983
- The biliary and urinary metabolites of [3H]17α-ethynylestradiol in womenXenobiotica, 1983
- The biotransformation of 17α-ethynyl[3H]estradiol in the rat: Irreversible binding and biliary metabolitesXenobiotica, 1982
- Comparative Study of Ethynyloestradiol Metabolism in the Rabbit, Guinea Pig and RatHormone Research, 1979
- Metabolism of 17α-Ethinylestradiol by Human Liver Microsomesin Vitro: Aromatic Hydroxylation and Irreversible Protein Binding of MetabolitesJournal of Clinical Endocrinology & Metabolism, 1974
- Studies on the Metabolism of Ethynylestradiolin vitroandin vivo: The Significance of 2-Hydroxylation and the Formation of Polar ProductsXenobiotica, 1973
- 2,4-Dibromo-α-oestradiolJournal of the American Chemical Society, 1940