Steroids, XLVII: A facile synthesis of 3β-hydroxy-5α-cholest-8(14)-en-15-one
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry
Reference14 articles.
1. N-arylurethane neighboring group participation during solvolysis of 3-methoxy-17-N-phenylcarbamoyloxy-16-p_tolylsulfonyloxymethylestra-1,3,5(10)-triene stereoisomers
2. A novel synthesis of 3β-hydroxy-5α-cholest-8(14)-en-15-one
3. Improved preparation of (3.beta.,5.alpha.,14.alpha.)-3-hydroxy-14-methylcholest-7-en-15-one. Synthesis of ergostenone and 20.alpha.-(hydroxymethyl)pregnenone analogs
4. Concerning the chemical synthesis of 3β-hydroxy-5α-cholest-8(14)-en-15-one, a novel regulator of cholesterol metabolism
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1. Two approaches to 14,15-secoergostane intermediates for the synthesis of strophasterols;Bioscience, Biotechnology, and Biochemistry;2018-06-03
2. Review of progress in sterol oxidations: 1987–1995;Lipids;1996-05
3. Inhibitors of sterol synthesis. An improved chemical synthesis of 26-oxygenated Δ8(14)-15-ketosterols having the 25R configuration;Chemistry and Physics of Lipids;1994-05
4. Steroids: reactions and partial syntheses;Natural Product Reports;1994
5. Steroids 48. Synthesis of 16α-ethyl-21-hydroxy-19-norpregn-4-ene-3,20-dione from 17-substituted 3-methoxyestradiols;Steroids;1993-04
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