Abstract
In the primary electrochemical reduction of 1-(nitrophenyl)-3,5-dicarbethoxy-4-phenyl-1,4-dihydropyridine in DMF, free radicals of nitrophenyl type are formed; these are the products of a one-electron reduction of cathode-protonated molecules of the original compound. In alkaline DMF, where cathodic protonation of the initial compound is retarded, union-radicals of the starting material are generated in addition, together with p-nitrophenol free radicals.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1498–1505, November, 1992.
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Stradyn, Y., Baumane, L., Gavars, R. et al. Free radicals in electrochemical reduction of 1-(nitrophenyl)-3,5-dicarbethoxy-4-phenyl-1,4-dihydropyridines. Chem Heterocycl Compd 28, 1280–1285 (1992). https://doi.org/10.1007/BF00532078
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DOI: https://doi.org/10.1007/BF00532078