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Michael condensation of 3-arylidene-3H-pyrrol-2-ones and 3-arylidene-3H-furan-2-ones with cyclohexanone

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The Michael condensation in the series of 5-aryl-3-arylidene-3H-pyrrol-2-ones and 5-aryl-3-arylidene-3H-furan-2-ones, containing an activated C=C bond, with cyclohexanone was investigated. It was shown that the condensation products were 1,5-dicarbonyl compounds containing a heterocyclic fragment. The enolization of one of the oxo groups, leading to the formation of hydroxypyrrole or hydroxyfuran structures, was demonstrated by the spectral data.

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Authors and Affiliations

  1. N. G. Chernyshevskii Saratov State University, Saratov, 410012, Russia

    Z. Yu. Timofeeva & A. Yu. Yegorova

Authors
  1. Z. Yu. Timofeeva
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  2. A. Yu. Yegorova
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Correspondence to Z. Yu. Timofeeva.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 823–827, June, 2007.

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Timofeeva, Z.Y., Yegorova, A.Y. Michael condensation of 3-arylidene-3H-pyrrol-2-ones and 3-arylidene-3H-furan-2-ones with cyclohexanone. Chem Heterocycl Compd 43, 690–694 (2007). https://doi.org/10.1007/s10593-007-0112-z

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  • DOI: https://doi.org/10.1007/s10593-007-0112-z

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