Synthesis and spectral properties of coumaronyl-substituted benzo[<i>f</i>]quinolines

Authors

  • Н. Г. Козлов Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072
  • K. Н. Гусак Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072
  • С. А. Махнач Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072

Abstract

Condensation of arylidene-2-naphthylamines with 2-acetylbenzofuran (2-acetylcoumarone) was used for the first time to synthesize 1-(2-coumaronyl)-3-arylbenzol[f]quinolines containing two different heteroatoms — N and O — in the molecule. The IR, UV, ESR and mass spectra of the compounds obtained were studied.

How to Cite
Kozlov, N. G.; Gusak, K;.N.; Makhnach, S. A.  Chem. Heterocycl. Compd. 1996, 32, 822. [Khim. Geterotsikl. Soedin. 1996, 960.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165728

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Published

1996-07-25

Issue

No. 7 (1996)

Section

Original Papers