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Reactions of substituted 7-aminoindoles with 1,3-diketones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The condensation of 2,3-dimethyl and 1,2,3-trimethyl-7-aminoindoles withβ-dicarbonyl compounds leads to enaminoketones, which undergo cyclization by the action of trifluoroacetic acid giving substituted pyrrolo[3,2-h]quinolines.

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References

  1. S. A. Yamashkin, Khim. Geterotsikl. Soedin., No. 11, 1520 (1992).

  2. P. A. Sharbatyan, S. A. Yamashkin, A. N. Kost, and L. G. Yudin, Khim. Geterotsikl. Soedin., No. 1, 73 (1977).

  3. Zh. F. Sergeeva, R. N. Akhvlediani, V. P. Shatunova, B. A. Korolev, A. N. Vasil'ev, T. N. Babushkina, and N. N. Suvorov, Khim. Geterotsikl. Soedin, No. 12, 1656 (1975).

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Authors and Affiliations

  1. Mordovo State Pedagogic Institute, 430007, Saransk

    S. A. Yamashkin & I. A. Batanov

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  1. S. A. Yamashkin
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  2. I. A. Batanov
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 58–62, January, 1995.

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Yamashkin, S.A., Batanov, I.A. Reactions of substituted 7-aminoindoles with 1,3-diketones. Chem Heterocycl Compd 31, 50–53 (1995). https://doi.org/10.1007/BF01171290

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  • DOI: https://doi.org/10.1007/BF01171290

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