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Dual reactivity of 1,2-disubstituted dihydro-N-heteroaromatic systems. 6. Electrochemical oxidation of N-acyl derivatives of 2-phenyl-1,2-dihydroquinolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

In the electrochemical oxidation of 1-acyl-2-phenyl-1,2-dihydroquinolines, first the radical cations of the starting compounds form; these then lose a benzoyl radical and go over to the 2-arylquinoline cations.

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Authors and Affiliations

  1. Dnepropetrovsk Civil Engineering Institute, 320631, Dnepropetrovsk

    I. M. Sosonkin, A. K. Sheinkman, G. G. Vdovkina, T. S. Chmilenko & A. N. Domarev

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  1. I. M. Sosonkin
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  2. A. K. Sheinkman
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  3. G. G. Vdovkina
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  4. T. S. Chmilenko
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  5. A. N. Domarev
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Additional information

For Communication No. 5, see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 801–805, June, 1985.

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Sosonkin, I.M., Sheinkman, A.K., Vdovkina, G.G. et al. Dual reactivity of 1,2-disubstituted dihydro-N-heteroaromatic systems. 6. Electrochemical oxidation of N-acyl derivatives of 2-phenyl-1,2-dihydroquinolines. Chem Heterocycl Compd 21, 667–671 (1985). https://doi.org/10.1007/BF00515069

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  • DOI: https://doi.org/10.1007/BF00515069

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