Nucleophilic substitution in azasydnone-modified dinitroanisoles Научная публикация
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Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Вых. Данные | Год: 2025, Том: 35, Номер: 3, Страницы: 271-273 Страниц : 3 DOI: 10.71267/mencom.7614 | ||
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Реферат:
Reactions of 3-(4-methoxy-3,5-dinitrophenyl)-1,2,3,4-oxatriazolium-5-olate with N-nucleophiles under mild conditions results in the displacement of the methoxy group leaving 1,2,3,4-oxatriazolium-5-olate (azasydnone) moiety intact. In the case of alkylhydrazines, further cyclization involving nitro group into benzo[d][1,2,3]triazole 3-oxides occurs.
Библиографическая ссылка:
Shkineva T.K.
, Kormanov A.V.
, Dalinger I.L.
Nucleophilic substitution in azasydnone-modified dinitroanisoles
Mendeleev Communications. 2025. V.35. N3. P.271-273. DOI: 10.71267/mencom.7614 WOS Scopus OpenAlex
Nucleophilic substitution in azasydnone-modified dinitroanisoles
Mendeleev Communications. 2025. V.35. N3. P.271-273. DOI: 10.71267/mencom.7614 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:001501365000010 |
| ≡ Scopus: | 2-s2.0-105006796711 |
| ≡ OpenAlex: | W4409003307 |