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Free-radical and electrophilic functionalization of pyrazol-3-ones with C–O or C–N bond formation (microreview) Обзор

Журнал Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122
Вых. Данные Год: 2021, Том: 57, Номер: 2, Страницы: 134-136 Страниц : 3 DOI: 10.1007/s10593-021-02885-8
Авторы Lopat’eva Elena R. 1 , Krylov Igor B. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow, 119991, Russia

Реферат: Pyrazol-3-ones are known as a class of anti-inflammatory drugs and popular heterocycles in search for new bioactive substances. The electrophilic or freeradical functionalization of C-4 position of pyrazolin-3-ones with the formation of C–C, C–S, C–Hal, C–N, and C–O bonds has been extensively developed in the last decade. Among these methods, the C–O or C–N bond forming reactions are studied less. This microreview covers selected examples of such reactions published in the last 10 years.
Библиографическая ссылка: Lopat’eva E.R. , Krylov I.B.
Free-radical and electrophilic functionalization of pyrazol-3-ones with C–O or C–N bond formation (microreview)
Chemistry of Heterocyclic Compounds. 2021. V.57. N2. P.134-136. DOI: 10.1007/s10593-021-02885-8 WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:000624405400008
≡ Scopus: 2-s2.0-85102053911
≡ OpenAlex: W3134255890
Альметрики: