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Reaction of N-arylidene-2-naphthylamines with allylacetone

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction between N-arylidene-2-naphthylamines and allylacetone leads to the formation of 1,3-disubstituted benzo[f]quinolines having a butenyl radical in position 1. It is shown that the reaction proceeds via intermediate aminoketones — 1-(2-naphthylamine)-1-aryl-6-heptene-3-ones.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, Academy of Sciences of the Belorussian SSR, 220603, Minsk

    N. S. Kozlov, R. D. Sauts & V. A. Serzhanina

Authors
  1. N. S. Kozlov
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  2. R. D. Sauts
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  3. V. A. Serzhanina
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1519–1522, November, 1986.

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Kozlov, N.S., Sauts, R.D. & Serzhanina, V.A. Reaction of N-arylidene-2-naphthylamines with allylacetone. Chem Heterocycl Compd 22, 1229–1231 (1986). https://doi.org/10.1007/BF00471807

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  • DOI: https://doi.org/10.1007/BF00471807

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