Abstract
It was found by cyclic voltammetry and ESR that the excitation of the molecules of α,Β derivatives of Β-(5-nitro-2-furyl)-α-cyanoethylene in the radical-anion state by one-electron electrochemical reduction promotes chemical transformation of the other reaction centers, while preserving the nitrofuran group.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1636–1639, December, 1991.
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Gavar, R.A., Stradyn', Y.P., Baumane, L.K. et al. Free-radical intermediates in the electrochemical reduction of α,β derivatives of β-(5-nitro-2-furyl)-α-cyanoethylene. Chem Heterocycl Compd 27, 1312–1315 (1991). https://doi.org/10.1007/BF00515575
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DOI: https://doi.org/10.1007/BF00515575