9-Acetyl-(p-tolylcarbamoyl)aminoazafluorenes

In the case of 9-amino-3-methyl-2-azafluorene and 9-amino-4-azafluorene, which are formed in the reduction of the hydrazones and oximes of the corresponding azafluorenones with hydrazine hydrate in the presence of pyrophoric nickel, it was confirmed that 9-aminoazafluorenes are unstable. N-Acetyl and N-carbamoyl derivatives of the indicated 9-aminoazafluorenes were obtained. According to the PMR spectral data, 3-methyl-2-azafluorenone oxime is produced in the form of a mixture of Z and E isomers. Ketazines corresponding to 3-methyl-2-azafluorenone and 4-azafluorenone were synthesized. © 1984 Plenum Publishing Corporation.

Редакторы
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Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
7
Язык
Английский
Страницы
778-781
Статус
Опубликовано
Подразделение
-
Номер
-
Том
19
Год
1983
Организации
  • 1 Patrice Lumumba People's Friendship University, Moscow, 117923, Russian Federation
Ключевые слова
-
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/1414/