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The reactions of arylazasydnones with S- and O-nucleophiles Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122
Вых. Данные Год: 2023, Том: 59, Номер: 4-5, Страницы: 289-298 Страниц : 10 DOI: 10.1007/s10593-023-03195-x
Авторы Kormanov Alexandr V. 1 , Shkineva Tatyana K. 1 , Dalinger Igor L. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

Реферат: A series of 3-arylazasydnone derivatives containing a chlorine atom and nitro group at various phenyl ring locations were functionalized by a method developed on the basis of reactions with different S- and O-nucleophiles. In all cases, an SNAr reaction was shown to occur where the leaving group could be either a halogen or azasydnone moiety, depending on their mutual position.
Библиографическая ссылка: Kormanov A.V. , Shkineva T.K. , Dalinger I.L.
The reactions of arylazasydnones with S- and O-nucleophiles
Chemistry of Heterocyclic Compounds. 2023. V.59. N4-5. P.289-298. DOI: 10.1007/s10593-023-03195-x WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:001019068600008
≡ Scopus: 2-s2.0-85162248412
≡ OpenAlex: W4381490567
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