Novel epimerizatton of steroidal allylic alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference11 articles.
1. Formation of a steroidal allyl alcohol in the mammary glands of mice
2. Steroid Metabolism in the Normal Mammary Gland and in the Dimethylbenzanthracene-Induced Mammary Tumor of Rats*
3. The conversion of 17α-hydroxyprogesterone into pregn-4-en-3α,17α-diol-20-one and other substances by perfusions through bovine adrenals and ovaries
4. Studies on the Metabolism of Steroids in the Foetus. Biosynthesis of 3-Hydroxy-Delta4-C19 Steroids in the Human Foetal Liver
5. The Reversible Reduction of Testosterone to Androst-4-ene-3alpha, 17beta-diol by a Soluble Enzyme of Rat Liver
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1. “Eco-Friendly” Epimerization of Lutein to 3′-Epilutein Under Solvent-Free Mechanochemical Conditions by Using a Strongly Acidic Cation-Exchange Resin;European Journal of Organic Chemistry;2018-06-25
2. Improved syntheses of aromatase inhibitors and neuroactive steroids efficient oxidations and reductions at key positions for bioactivity;Tetrahedron;1999-03
3. Synthesis and oxidation of pregna-3,5-dien-20-ols and -20-one and selective reduction of pregna-3,5-dien-20-one;Liebigs Annalen der Chemie;1990-03-12
4. Reduction of testosterone, androstendione and their derivatives byAphanocladium album;Journal of Basic Microbiology;1989
5. Synthesis and characteristics of allylic 4-pregnene-3,20-diols found in gonadal and breast tissues;Steroids;1986-04
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