The reactions of arylazasydnones with S- and O-nucleophiles Научная публикация
| Журнал |
Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122 |
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| Вых. Данные | Год: 2023, Том: 59, Номер: 4-5, Страницы: 289-298 Страниц : 10 DOI: 10.1007/s10593-023-03195-x | ||
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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
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 |