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Rearrangement of the adducts of α-(aminocarbonyl)-acetamidoximes with acylacetylenes, leading to 2-aminopyrrole derivatives*

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Chemistry of Heterocyclic Compounds Aims and scope

The rearrangement and cyclization of O-vinylamidoximes, which are adducts of α-(aminocarbonyl)-acetamidoximes with acetylenic ketones, leads to 2-acylaminopyrroles.

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Authors and Affiliations

  1. St. Petersburg State University, 26 Universitetskaya nab., Saint Petersburg, 198504, Russia

    E. E. Pivneva, A. V. Galenko, D. V. Dar’in & P. S. Lobanov

Authors
  1. E. E. Pivneva
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  2. A. V. Galenko
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  3. D. V. Dar’in
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  4. P. S. Lobanov
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Corresponding author

Correspondence to P. S. Lobanov.

Additional information

*For preliminary communication, see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 942-947, June, 2012.

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Pivneva, E.E., Galenko, A.V., Dar’in, D.V. et al. Rearrangement of the adducts of α-(aminocarbonyl)-acetamidoximes with acylacetylenes, leading to 2-aminopyrrole derivatives*. Chem Heterocycl Comp 48, 875–880 (2012). https://doi.org/10.1007/s10593-012-1069-0

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