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.

Authors
Prostakov N.S. 1 , Kholdarova T. 1 , Pleshakov V.G. 1 , Govor S.Ya. 1 , Shalimov V.P. 1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Issue number
3
Language
English
Pages
323-326
State
Published
Volume
9
Year
1975
Organizations
  • 1 Patrice Lumumba University, Moscow, Russian Federation
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