A General Route to 3-Thiosubstituted Steroids via Copper-Catalyzed C-S Coupling

A convenient and efficient approach to 3-thiosubstituted androstanes has been developed. The formation of a C(sp 2)-S bond was achieved through the Cu-catalyzed coupling of steroidal iododienes with a variety of S-nucleophiles, such as (het)aryl thiols and dithiocarbamates. A simple catalytic system comprising CuI without auxiliary ligands enabled the preparation of a library of target compounds in good to high yields. A moderate inhibitory activity against hormone-dependent cancer cell lines was demonstrated for representative 3-thiolated steroids. © 2025 Elsevier B.V., All rights reserved.

Авторы
Parulava Mikhail J. 1 , Kotovshchikov Yury N. 1 , Latyshev Gennadij V. 1 , Sokolova Darina V. 2, 3 , Lukashev Nikolay V. 1 , Beletskaya Irina Petrovna 1
Журнал
Издательство
Georg Thieme Verlag
Номер выпуска
8
Язык
Английский
Страницы
1481-1489
Статус
Опубликовано
Том
57
Год
2025
Организации
  • 1 Department of Chemistry, Lomonosov Moscow State University, Moscow, Russian Federation
  • 2 RUDN University, Moscow, Russian Federation
  • 3 Blokhin National Medical Research Center of Oncology, Ministry of Health, Moscow, Russian Federation
Ключевые слова
catalysis; copper; dithiocarbamates; heterocycles; steroids; thiols
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