Pyrrolo[3,2-c]piperidines

The heterocyclization reaction of oximes derived from aliphatic ketones with acetylene has been applied to piperidone oximes. Pyrrole[3,2-c]piperidines substituted on the six-membered ring have been prepared in this manner. Assumptions have been made concerning their conformational and configurational properties. These reactions have been demonstrated to lead to the formation of condensed systems containing a pyrrolenine fragment. © 1988 Plenum Publishing Corporation.

Authors
Borisova T.N. 1 , Varalmov A.V. 1 , Sergeeva N.D. 1 , Soldatenkov A.T. 1 , Zvolinskii O.V. 1 , Astakhov A.A. 1 , Prostakov N.S. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
7
Language
English
Pages
799-803
Status
Published
Link
External link
DOI
10.1007/BF00475655
Volume
23
Year
1987
Organizations
  • 1 Patrice Lumumbii People's Friendship University, Moscow, 117923, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1293/
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SYNTHESIS OF 4-SUBSTITUTED 1-METHYL(BENZYL)-2,5-DIMETHYL-4-R-AMINOPIPERIDINES

Article
Kuznetsov V.V., Gaivoronskaya L.A., Romero R.M., Stashenko E.E., Zakharov P.I., Prostatkov N.S.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 23. 1987. P. 783-786