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New stereoselective synthesis of 5α-androst-1-ene-3β,17β-diol Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2023, Том: 72, Номер: 11, Страницы: 2726-2730 Страниц : 5 DOI: 10.1007/s11172-023-4078-5
Авторы Chernoburova E.I. 1 , Shchetinina M.A. 1 , Korolev V.A. 1 , Ilovaisky A.I. 1 , Zavarzin I.V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Реферат: Efficient stereoselective methods for the synthesis of 5α-androst-1-ene-3β,17β-diol, which is used as a reference compound for identification of anabolic steroids and their metabolites, were elaborated. The key factor of the synthesis is the use of the sodium borohydride—cerium(III) chloride system as a reducing agent.
Библиографическая ссылка: Chernoburova E.I. , Shchetinina M.A. , Korolev V.A. , Ilovaisky A.I. , Zavarzin I.V.
New stereoselective synthesis of 5α-androst-1-ene-3β,17β-diol
Russian Chemical Bulletin. 2023. V.72. N11. P.2726-2730. DOI: 10.1007/s11172-023-4078-5 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001132088500016
Scopus: 2-s2.0-85180649173
OpenAlex: W4390416064
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OpenAlex Нет цитирований
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