Transformations of 2,6-dimethyl- and 2,3-dimethyl-6-ethyl-4-(2′-furyl)pyridines involving the furan and pyridine rings

Alkyl-substituted 4-(2′-furyl)pyridines are brominated and nitrated in the C5' position of the furan ring; however, they do not undergo electrophilic substitution reactions such as acetylation, formylation, and chloro- and aminomethylation. Furyl-substituted indolizines and tetrahydropyridines were obtained from quaternary salts of 2,6-dimethyl-4-(2′-furyl)pyridine. © 1983 Plenum Publishing Corporation.

Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
12
Язык
Английский
Страницы
1287-1289
Статус
Опубликовано
Подразделение
-
Номер
-
Том
18
Год
1982
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/1438/