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Rearrangement of O-vinyl-α-(amino-carbonyl)acetamidoximes to 2-aminopyrroles and 2-pyrrolinones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Rearrangement and cyclization of O-vinyl-α-(aminocarbonyl)acetamidoximes gives two isomeric 2-aminopyrroles and/or 2-pyrrolinones and this depends on the rearrangement route.

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References

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Authors and Affiliations

  1. St. Petersburg State University, St. Petersburg, 198504, Russia

    A. V. Galenko, S. I. Selivanov, P. S. Lobanov & A. A. Potekhin

Authors
  1. A. V. Galenko
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  2. S. I. Selivanov
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  3. P. S. Lobanov
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  4. A. A. Potekhin
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Corresponding author

Correspondence to P. S. Lobanov.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1328–1334, September, 2007.

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Galenko, A.V., Selivanov, S.I., Lobanov, P.S. et al. Rearrangement of O-vinyl-α-(amino-carbonyl)acetamidoximes to 2-aminopyrroles and 2-pyrrolinones. Chem Heterocycl Comp 43, 1124–1130 (2007). https://doi.org/10.1007/s10593-007-0173-z

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  • DOI: https://doi.org/10.1007/s10593-007-0173-z

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