The nature of the final oxidative step in the aromatization sequence
- 31 December 1987
- Vol. 50 (4-6), 339-345
- https://doi.org/10.1016/0039-128x(87)90023-7
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Mechanistic studies on C-19 demethylation in oestrogen biosynthesisBiochemical Journal, 1982
- Localization of Estrogen Synthetase in the Chorionic Villus Fraction After Homogenization of Human Term PlacentaJournal of Clinical Endocrinology & Metabolism, 1977
- Reassignment of the absolute configuration of 19-substituted 19-hydroxysteroids and stereomechanism of estrogen biosynthesisJournal of the American Chemical Society, 1975
- Conversion of an androgen epoxide into 17β-estradiol by human placental microsomesBiochemistry, 1975
- Unusually facile aromatization of 2.beta.-hydroxy-19-oxo-4-androstene-3,17-dione to estrone. Implications in estrogen biosynthesisJournal of the American Chemical Society, 1974
- Formation of Steroids by the Pregnant Mare. IV. Metabolism 14 of C-Mevalonic Acid and 3 H-Dehydroisoandrosterone Injected into the Fetal Circulation14Endocrinology, 1973
- Stereochemistry of estrogen biosynthesisJournal of the American Chemical Society, 1969
- Mechanism of estrogen biosynthesis. VI. The stereochemistry of hydrogen elimination at C-2 during aromatizationJournal of the American Chemical Society, 1969
- Mechanism of estrogenbiosynthesis. III. Stereochemistry of aromatization of C19 and C18 steroidsBiochemistry, 1968
- Conversion of 19-hydroxy-Δ4-androstene-3,17-dione to estrone by endocrine tissueBiochimica et Biophysica Acta, 1955