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Synthesis and spectral properties of coumaronyl-substituted benzo[f]quinolines

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Chemistry of Heterocyclic Compounds Aims and scope

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.

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Authors
  1. N. G. Kozlov
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  2. K. N. Gusak
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  3. S. A. Makhnach
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Additional information

Institute of Organophysical Chemistry, Belorussian Academy of Sciences, Minsk 220072. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 960–964, July, 1996. Original article submitted April 18, 1996.

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Kozlov, N.G., Gusak, K.N. & Makhnach, S.A. Synthesis and spectral properties of coumaronyl-substituted benzo[f]quinolines. Chem Heterocycl Compd 32, 822–825 (1996). https://doi.org/10.1007/BF01165728

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