The phenylation of 3βpicoline. Isolation and establishment of the structure of β-pyridyl-α-dehydropiperidine

It was established that the side product that is formed in substantial amounts in the phenylation of β-picoline by phenyllithium is 3-methyl-2-phenyl-5-(3-methyl-2-phenyl-3,4-dehydropiperidyl-6)pyridine - a structural analog of anabasine. Its structure was demonstrated by spectral methods and by chemical conversions. © 1985 Plenum Publishing Corporation.

Авторы
Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
8
Язык
Английский
Страницы
911-915
Статус
Опубликовано
Подразделение
-
Номер
-
Том
20
Год
1984
Организации
  • 1 P. 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/1383/