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Chemistry of Heterocyclic Compounds

, Volume 32, Issue 9, pp 1047–1051 | Cite as

Free radicals in the electrochemical reduction of 1,2-dihydro-3-nitropyridine derivatives

  • Ya. Stradyn'
  • R. Gavats
  • L. Baumane
  • B. Vigante
  • G. Duburs
Article

Abstract

The formation of primary radical anions of N-substituted 1, 2-dihydro-3-nitropyridines was confirmed by the ESR method under conditions of electrochemical generation of free radicals, and their structure was established. The causes of the different ability of 1,2- and 1,4-dihydro-3-nitropyridines to form free radicals during electrochemical reduction that are stable enough to be studied by the ESR method are examined.

Keywords

Organic Chemistry Free Radical Radical Anion Electrochemical Reduction Electrochemical Generation 
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 1997

Authors and Affiliations

  • Ya. Stradyn'
  • R. Gavats
  • L. Baumane
  • B. Vigante
  • G. Duburs

There are no affiliations available

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