Nitration of benzo[g]isoquinoline and its methyl-substituted derivatives

Di- and trinitro derivatives are formed in the nitration under mild conditions (0-5 °C) of benzo[g]isoquinoline and its analogs with a methyl substituent in the pyridine and phenylene rings. The principal reaction products contain a nitro group in the meso position (attached to the C5 atom) and in the phenylene ring. The structures of the nitro derivatives obtained and the position of the nitro groups in the molecules were proved by means of the PMR, IR, and mass spectra. © 1982 Plenum Publishing Corporation.

Авторы
Prostakov N.S. 1 , Datta Rai G. , Sergeeva N.D. 1 , Kuznetsov V.I. 1
Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
12
Язык
Английский
Страницы
1217-1220
Статус
Опубликовано
Подразделение
-
Номер
-
Том
17
Год
1981
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/1483/