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Conversion of pyrrolo[1,2-α]pyrazinium salts to 8-aminoindolizines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The recyclization of pyrrolo[1,2-a]pyrazinium salts under the influence of a base leads to 8-aminoindolizine derivatives and is a new method for the synthesis of indolizines, as well as the first example of the Kost—Sagitullin rearrangement in the pyrazine series.

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Literature Cited

  1. V. I. Terenin, E. V. Kabanova, E. S. Feoktistova, and Yu. G. Bundel', Khim. Geterotsikl. Soedin., No. 3, 424 (1989).

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Authors and Affiliations

  1. M. V. Lomonosov Moscow State University, 119899, Moscow

    V. I. Terenin, E. V. Kabanova & Yu. G. Bundel'

Authors
  1. V. I. Terenin
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  2. E. V. Kabanova
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  3. Yu. G. Bundel'
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Additional information

See [1] for our preliminary communication.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 763–766, June, 1991.

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Terenin, V.I., Kabanova, E.V. & Bundel', Y.G. Conversion of pyrrolo[1,2-α]pyrazinium salts to 8-aminoindolizines. Chem Heterocycl Compd 27, 597–600 (1991). https://doi.org/10.1007/BF00472505

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  • DOI: https://doi.org/10.1007/BF00472505

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