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Catalytic alkylation of substituted indoles with (phenothiazin-10-yl)propene-1-ones

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Abstract

Alkylation of substituted indoles (carbazoles, tetrahydrocarbazoles, and gamma-carbolines) with (phenothiazinyl)propenones catalyzed by cesium fluoride has led to the formation of 1-(phenothiazin-10-yl)-3-(carbazol-9-yl)propane-1-ones, (1-phenothiazin-10-yl)-3-(tetrahydrocarbazol-9-yl)propane-1-ones, and 3-(tetrahydropyrido[4,3-b]indol-5-yl)-1-(phenothiazin-10-yl)propane-1-ones, respectively.

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Authors and Affiliations

  1. Institute of Physiologically Active Compounds, Russian Academy of Sciences, Severnyi pr. 1, Chernogolovka, 142432, Russia

    V. B. Sokolov, A. Yu. Aksinenko, T. A. Epishina & T. V. Goreva

Authors
  1. V. B. Sokolov
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  2. A. Yu. Aksinenko
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  3. T. A. Epishina
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  4. T. V. Goreva
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Corresponding author

Correspondence to A. Yu. Aksinenko.

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Original Russian Text © V.B. Sokolov, A.Yu. Aksinenko, T.A. Epishina, T.V. Goreva, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 5, pp. 763–766.

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Sokolov, V.B., Aksinenko, A.Y., Epishina, T.A. et al. Catalytic alkylation of substituted indoles with (phenothiazin-10-yl)propene-1-ones. Russ J Gen Chem 86, 1028–1031 (2016). https://doi.org/10.1134/S1070363216050078

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  • DOI: https://doi.org/10.1134/S1070363216050078

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