Condensation of 1,2,5-trimethyl-4-piperidone with ethyl- and naphthylacetylenes and synthesis of substituted pyridines

The Favorskii reaction with 1,2,5-trimethyl-4-piperidone and ethyl- and naphthylacetylenes gave the corresponding piperidols, the hydrogenation of which gave 1,2,5-trimethyl-4-nbutyl(or 2-naphthylethyl)-4-piperidols. 4-Phenyl- and 4-butyl-2,5-dimethylpyridine were condensed with formaldehyde, and some of the transformations of the resulting β-hydroxyethyl derivatives were studied. © 1975 Plenum Publishing Corporation.

Авторы
Prostakov N.S. 1 , Kholdarova T.1 , Pleshakov V.G. 1 , Govor S.Ya.1 , Shalimov V.P. 1
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
3
Язык
Английский
Страницы
323-326
Статус
Опубликовано
Том
9
Год
1975
Организации
  • 1 Patrice Lumumba University, Moscow, Russian Federation
Цитировать
Поделиться

Другие записи

Prostakov N.S., Ismailov A.Ya., Zvolinskii V.P.
Химия гетероциклических соединений. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Том 9. 1975. С. 907-910