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Synthesis of 3-(2-pyrrolyl)indoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

New 3-(2-pyrrolyl)indole systems were synthesized on the basis of heterocyclization of 3-acylindole oximes with acetylene in a superbase medium (the Trofimov reaction). It is shown that only the anti form of the oxime participates in the formation of the pyrrole ring.

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Literature cited

  1. B. A. Trofimov and A. I. Mikhaleva, Khim. Geterotsikl. Soedin., No. 10, 1299 (1980).

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Authors and Affiliations

  1. M. V. Lomonosov Moscow State University, 117234, Moscow

    M. A. Yurovskaya, V. V. Druzhinina, E. V. Snetkova & Yu. G. Bundel'

Authors
  1. M. A. Yurovskaya
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  2. V. V. Druzhinina
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  3. E. V. Snetkova
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  4. Yu. G. Bundel'
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 356–360, March, 1983.

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Yurovskaya, M.A., Druzhinina, V.V., Snetkova, E.V. et al. Synthesis of 3-(2-pyrrolyl)indoles. Chem Heterocycl Compd 19, 289–292 (1983). https://doi.org/10.1007/BF00513262

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  • DOI: https://doi.org/10.1007/BF00513262

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