ESR spectra of free radicals of 3,3-disubstituted 1,2,3,4-tetrahydropyridines produced during electrochemical reduction

Authors

  • P. Гaварс Latvian Institute of Organic Synthesis, Riga LV-1006
  • Л. Баумане Latvian Institute of Organic Synthesis, Riga LV-1006
  • Я. Страдынь Latvian Institute of Organic Synthesis, Riga LV-1006
  • Б. Чекавичус Latvian Institute of Organic Synthesis, Riga LV-1006
  • Г. Дубурс Latvian Institute of Organic Synthesis, Riga LV-1006

Abstract

The polarographic properties (potentials, number of electrons, reversibility) of the electrochemical reduction of 3,5-diethoxycarbonyl-3-(p-nitrobenzoyl)-6-(p-nitrophenyl)-1,2,3,4-tetrahydropyridine and its derivatives in dimethylformamide have been determined. In the course of the electrochemical generation, ESR spectra of primary radical anions of p-nitrobenzoyl structure were obtained along with ESR spectra of nitrophenyl-p-substituted free radicals formed as a result of further reduction.

How to Cite
Gavars, R.; Baumane, L.; Stradyn, Y.; Chekavichus, B.; Duburs, G. Chem. Heterocycl. Compd. 1998, 34, 950. [Khim. Geterotsikl. Soedin. 1998, 34, 1103.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02311332

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Published

1998-08-25

Issue

No. 8 (1998)

Section

Original Papers