3-Azafluorenes with nitrogen-containing substituents in the C9 position

In the case of the reaction of 9-bromo-4-azafluorene with 2, 5-dimethyl-4-piperidone and p-anisidine it was confirmed that the reactions of this bromide with secondary aliphatic and primary aromatic amines proceed via different mechanisms. Propionyl and phenylcarbamoyl derivatives of 9-bis (β-hydroxy-ethyl) amino-4-azafluorene were synthesized. Spectral data on the pseudoazulenes formed from 9-morpholino-4-aza-fluorene mono- and dimethiodide were obtained. © 1986 Plenum Publishing Corporation.

Авторы
Prostakov N.S. 1 , Montenegro Cordova G.B. , Shalimov V.P. 1
Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
10
Язык
Английский
Страницы
1148-1150
Статус
Опубликовано
Подразделение
-
Номер
-
Том
21
Год
1985
Организации
  • 1 Patrice Lumumba Peoples' 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/1357/