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Chemistry of Heterocyclic Compounds

, Volume 17, Issue 3, pp 261–267 | Cite as

Enamines. 9. Polarographic reduction of enamino ketones in aqueous media

  • M. K. Polievktov
  • S. S. Kiselev
  • I. G. Markova
  • V. G. Granik
Article
  • 32 Downloads

Abstract

The mechanism of the polarographic reduction of cyclic enamino ketones of the pyrrolidine, piperidine, and hexahydroazepine series of two types, viz., compounds in which the α-carbon atom of the enamine is included in the azoheteroring, and enamino ketones in which the double bond is located outside the cyclic system, was investigated. The acyclic analogs were also studied. It is shown that the two- or four-electron reduction depends substantially on the structures of the investigated compounds and the pH of the medium; this in turn is associated with a change in the character, rate, and site of protonation of the enamino ketones and the compounds formed as a result of their reduction.

Keywords

Organic Chemistry Ketone Double Bond Aqueous Medium Piperidine 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Publishing Corporation 1981

Authors and Affiliations

  • M. K. Polievktov
    • 1
  • S. S. Kiselev
    • 1
  • I. G. Markova
    • 1
  • V. G. Granik
    • 1
  1. 1.S. Ordzhonikidze All-Union Scientific-Research Institute of Pharmaceutical ChemistryMoscow

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