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Oxidation-reduction Conversions of 1,4-Dihydropyridine Derivatives on Interaction of Alicyclic 1,5-Diketones with Nitroanilines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

On interaction of alicyclic 1,5-diketones and the products of their intramolecular aldol condensation with 2- and 4-nitroanilines and 2,4-dinitroaniline reduction occurs of the nitro group by the intermediately formed 1,4-dihydropyridine derivatives. The reaction products are N-nitrophenyl- and N-aminophenylpyridinium salts and also N,N-phenylenebispyridinium salts.

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Authors and Affiliations

  1. Far Eastern State University, Vladivostok, 690600, Russia

    K. V. Maslov, A. G. Egorov, T. I. Akimova & V. A. Kaminski

Authors
  1. K. V. Maslov
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  2. A. G. Egorov
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  3. T. I. Akimova
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  4. V. A. Kaminski
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Maslov, K.V., Egorov, A.G., Akimova, T.I. et al. Oxidation-reduction Conversions of 1,4-Dihydropyridine Derivatives on Interaction of Alicyclic 1,5-Diketones with Nitroanilines. Chemistry of Heterocyclic Compounds 38, 560–563 (2002). https://doi.org/10.1023/A:1019509212864

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  • DOI: https://doi.org/10.1023/A:1019509212864

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