Oxyfunctionalization of (5β)-Bile Acids by Dimethyldioxirane: Hydroxylation at C-5, C-14, and C-17
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Bile salts as biological surfactants
2. 5 beta-hydroxylation by the liver. Identification of 3,5,7-trihydroxy nor-bile acids as new major biotransformation products of 3,7-dihydroxy nor-bile acids in rodents
3. A highly regio- and stereoselective C5 oxyfunctionalization of coprostane steroids by dioxiranes: An improved access to progestogen and androgen hormones.
4. Selective Oxidation of Unactivated 5β C-H Bonds in Steroids by Dimethyldioxirane
5. Direct Oxyfunctionalization at Unactivated Sites. Synthesis of 5.beta.-Hydroxysteroids by Perfluorodialkyloxaziridines
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3. Dimethyldioxirane (DDO);Encyclopedia of Reagents for Organic Synthesis;2021-02-03
4. Dioxirane Oxidations of Compounds other than Alkenes;Oxidation of Organic Compounds by Dioxiranes;2014-08-11
5. Functionalization of Homodiamantane: Oxygen Insertion Reactions without Rearrangement with Dimethyldioxirane;The Journal of Organic Chemistry;2014-01-30
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