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Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles Научная публикация

Журнал Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Вых. Данные Год: 2002, Том: 12, Номер: 5, Страницы: 198-200 Страниц : 3 DOI: 10.1070/mc2002v012n05abeh001641
Авторы Vinogradov Vasilii M. 1 , Starosotnikov Aleksei M. 1 , Shevelev Svyatoslav A. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Реферат: The title compounds were prepared by the reactions of picrylacetaldehyde with aryldiazonium salts followed by the intramolecular cyclization of the resulting picrylglyoxal monoarylhydrazones, and the regiospecific substitution for the nitro group at the 4-position under the action of anionic N-, O- and S-nucleophiles was found.
Библиографическая ссылка: Vinogradov V.M. , Starosotnikov A.M. , Shevelev S.A.
Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles
Mendeleev Communications. 2002. V.12. N5. P.198-200. DOI: 10.1070/mc2002v012n05abeh001641 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000179887800015
Scopus: 2-s2.0-0036763720
OpenAlex: W1963872707
Цитирование в БД:
БД Цитирований
OpenAlex 12
Scopus 18
Web of science 21
Альметрики: