NMR parameters, isomerism, and conformational analysis of 3-methyl-2-phenyl-5-(3-methyl-2-phenyl-3,4-dehydropiperid-6-yl)-pyridine

The configurational and conformational features of the trans and cis isomers of 3-methyl-2-phenyl-5-(3-methyl-2-phenyl-3,4-dehydropiperid-6-yl)pyridine, formed as by-products in the phenylation of β-picoline by phenyllithium, were established. The revealed stereospecificity of the 5JHH and 1JCH SSCCs may be utilized as an independent criterion in the conformational analysis of piperideine systems. © 1993 Plenum Publishing Corporation.

Авторы
Aliev A.E.1 , Sinitsyna A.A.1 , Kirillova L.M.1 , Prostakov N.S. 1
Редакторы
-
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
1
Язык
Английский
Страницы
61-64
Статус
Опубликовано
Подразделение
-
Номер
-
Том
29
Год
1993
Организации
  • 1 Russian University of the Friendship of Peoples, Moscow, 117927, Russian Federation
Ключевые слова
-
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/1012/