Preparation of α- and γ-(α-furyl)pyridines

Mixtures of isomeric alkyl-substituted (in the pyridine ring) α- and γ-(α-furyl)-pyridines were obtained in up to ∼40% yields by condensation of furfural and ammonia with several aliphatic ketones and aldehydes (at 370-380 °C with a cadmium calcium phosphate catalyst). The dependence of the yields and structures of the corresponding isomers on the structure of the starting carbonyl compound was examined. Data from the PMR and mass spectra were used to prove the structures of the pyridine bases obtained. © 1981 Plenum Publishing Corporation.

Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
3
Язык
Английский
Страницы
284-289
Статус
Опубликовано
Подразделение
-
Номер
-
Том
17
Год
1981
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/1497/