OXIDATION–REDUCTION CONVERSIONS OF 1,4-DIHYDROPYRIDINE DERIVATIVES ON INTERACTION OF ALICYCLIC 1,5-DIKETONES WITH NITROANILINES

Authors

  • К. В. Маслов Far Eastern State University, Vladivostok 690600
  • А. Г. Егоров Far Eastern State University, Vladivostok 690600
  • Т. И. Акимова Far Eastern State University, Vladivostok 690600
  • В. А. Каминский Far Eastern State University, Vladivostok 690600

Keywords:

alicyclic 1,5-diketones, 2,4-dinitroaniline, 2-nitroaniline, 4-nitroaniline, pyridinium salts, reduction

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.

How to Cite
Maslov, K. V.; Egorov, A. G.; Akimova, T. I.; Kaminski, V. A. Chem. Heterocycl. Compd. 2002, 38, 560. [Khim. Geterotsikl. Soedin. 2002, 642.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1019509212864

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Published

2002-05-25

Issue

No. 5 (2002)

Section

Original Papers