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

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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.

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Latvian Institute of Organic Synthesis, Riga LV-1006. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1103–1110, August, 1998.

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Gavars, R., Baumane, L., Stradyn, Y. et al. ESR spectra of free radicals of 3,3-disubstituted 1,2,3,4-tetrahydropyridines produced during electrochemical reduction. Chem Heterocycl Compd 34, 950–956 (1998). https://doi.org/10.1007/BF02311332

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  • DOI: https://doi.org/10.1007/BF02311332

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