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Polyaralkylation of primary aromatic amines with 6-hybroxy-2,4-dimethyl-1,3-benzodioxane Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1983, Том: 19, Номер: 10, Страницы: 1053-1056 Страниц : DOI: 10.1007/BF00505750
Авторы Denisov V. Ya. , Fokin E. P.
Организации
1 (Scopus) Keremovo State University, Keremovo, 650043
2 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: 6-Hydroxy-2,4-dimethyl-1,3-benzodioxane is cleaved with opening of the 1,3-dioxane ring in a mixture of acetic and hydrochloric acids. The resulting hydroquinonecontaining fragments N-aralkylate the primary amines (aminoanthraquinone, p-nitroaniline, and p-aminoazobenzene) which are added to the reaction mixture to give the corresponding N-(polyethylidenehydroquinone)arylamines. © 1984 Plenum Publishing Corporation.
Библиографическая ссылка: Denisov V.Y. , Fokin E.P.
Polyaralkylation of primary aromatic amines with 6-hybroxy-2,4-dimethyl-1,3-benzodioxane
Chemistry of Heterocyclic Compounds. 1983. V.19. N10. P.1053-1056. DOI: 10.1007/BF00505750 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 окт. 1983 г.
Идентификаторы БД:
Scopus: 2-s2.0-34250135888
РИНЦ: 30919338
OpenAlex: W1991200711
Цитирование в БД: Пока нет цитирований
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