Azo-coupling reaction of anthra-1,3-oxazines with aromatic diazo compounds Научная публикация
| Журнал |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230 |
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| Вых. Данные | Год: 1965, Том: 14, Номер: 11, Страницы: 2043-2045 Страниц : 3 DOI: 10.1007/BF00845916 | ||
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Реферат:
1. The acyl derivatives of anthra-1,3-oxazine (I) enter into the azo-coupling reaction with aromatic diazo compounds; here the diazo group enters in the p-position to the tertiary nitrogen atom of the anthra-1,3-oxazine. 2. The arylazoanthra-1,3-oxazines (II) by hydrolytic cleavage of the 1,3-oxazine ring and the action of air are converted to the arylazo derivatives of N-1-anthraquinonyl-δ-aminovaleraldehyde. © 1966 Consultants Bureau.
Библиографическая ссылка:
Fokin E.P.
, Denisov V.Y.
Azo-coupling reaction of anthra-1,3-oxazines with aromatic diazo compounds
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1965. V.14. N11. P.2043-2045. DOI: 10.1007/BF00845916 Scopus
Azo-coupling reaction of anthra-1,3-oxazines with aromatic diazo compounds
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1965. V.14. N11. P.2043-2045. DOI: 10.1007/BF00845916 Scopus
Даты:
| Опубликована в печати: | 1 нояб. 1965 г. |
Идентификаторы:
| Scopus | 2-s2.0-34250604148 |
| OpenAlex | W2069208834 |