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. Thieme. All rights reserved.

Авторы
Parulava M.J. , Kotovshchikov Y.N. , Latyshev G.V. , Sokolova D.V. , Lukashev N.V. , Beletskaya I.P.
Журнал
Язык
Английский
Статус
Опубликовано
Номер
SS-2024-11-0457-OP
Год
2025
Организации
  • 1 Chemistry Department, M. V. Lomonosov Moscow State University, 1/3 Leninskiye Gory, Moscow, 119991, Russian Federation
  • 2 RUDN University, 6 Miklukho-Maklaya str., Moscow, 117198, Russian Federation
  • 3 N. N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of Russia, 24 Kashirskoe Shosse, Moscow, 115478, Russian Federation
Ключевые слова
catalysis; copper; dithiocarbamates; heterocycles; steroids; thiols
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