Synthesis and nitration of 4,6(4,8)-dimethyl-4-methyl-6(8)-methoxy-1,2,3,4-tetrahydrospiro [quinoline-2-cyclohexanes]

The cydization of 1-allyl-1-arylaminocyclohexanes under conditions of acid catalysis afforded 1,2,3,4-tetrahydro-4-methylspiro [quinoline-2-cyclohexanes] methyl (methoxy)-substituted in the phenylene ring. Their mono- and dinitro derivatives were synthesized, and their structure was established. Propositions on the direction of the nitration reaction of these heterocyclic compounds were expressed. © 1994 Plenum Publishing Corporation.

Авторы
Kuznetsov V.V. 1 , Pal'ma A. 1 , Aliev A.E.1 , Fernandes M.1 , Prostakov N.S. 1 , Varlamov A.V. 1
Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
6
Язык
Английский
Страницы
671-675
Статус
Опубликовано
Подразделение
-
Номер
-
Том
29
Год
1993
Организации
  • 1 Russian University of the Friendship of Peoples, Moscow, 117198, Russian Federation
Ключевые слова
-
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/996/