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Mannich Reaction of Solasodine with Acetylenes and Formaldehyde. Cytotoxicity of N-Propargyl-Substituted Alkaloid Derivatives Научная публикация

Журнал Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Вых. Данные Год: 2023, Том: 59, Номер: 1, Страницы: 87-93 Страниц : 7 DOI: 10.1007/s10600-023-03924-w
Ключевые слова steroidal alkaloids, solasodine, acetylene, Mannich reaction, cytotoxicity
Авторы Finke A.O. 1 , Mironov M.E. 1,2 , Pokrovskii M.A. 2 , Shults E.E. 1
Организации
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences
2 Novosibirsk State University

Реферат: The reaction of the steroidal alkaloid solasodine with formaldehyde, terminal arylalkynes, 2-ethynylpyridine, propiolic acid methyl ester, or (trimethylsilyl)acetylene with heating to 100°C in 1,4-dioxane in the presence of CuI synthesized the corresponding N-(prop-2-ynyl)spiro solanes as mixtures of (22R,25R)- and (22S,25R)-diastereomers in 28–81% yields and 1.6–1:1–1.7 ratios of stereoisomers. The cytotoxicities of the new solasodine derivatives against T98G, U-87, MT-4, and MDA-MB-231 human tumor cells were tested in vitro.
Библиографическая ссылка: Finke A.O. , Mironov M.E. , Pokrovskii M.A. , Shults E.E.
Mannich Reaction of Solasodine with Acetylenes and Formaldehyde. Cytotoxicity of N-Propargyl-Substituted Alkaloid Derivatives
Chemistry of Natural Compounds. 2023. V.59. N1. P.87-93. DOI: 10.1007/s10600-023-03924-w WOS РИНЦ OpenAlex
Даты:
Поступила в редакцию: 10 июн. 2022 г.
Опубликована в печати: 28 февр. 2023 г.
Идентификаторы БД:
Web of science: WOS:000941326300004
РИНЦ: 61460259
OpenAlex: W4322775392
Цитирование в БД: Пока нет цитирований
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