Reduction of quaternary salts of 3-azafluorene and 3-azafluorenone and their conversion to indenoindolizines

The tetrahydro and hexahydro derivatives with respect to the nitrogen-containing ring were obtained by reduction of 3-azafluorene and 3-azafluorenone methiodides, respectively, with sodium borohydride. Indenoindolizines with linear and angular structures were synthesized from the N-phenacyl quaternary salts of 3-azafluorenones via 1,3-dipolar cycloaddition and by the Chichibabin method. 7-Nitro-3-azafluorenone and 3-azafluorenone N-oxide were obtained. © 1983 Plenum Publishing Corporation.

Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
2
Язык
Английский
Страницы
206-209
Статус
Опубликовано
Подразделение
-
Номер
-
Том
19
Год
1983
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/1423/