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Chemistry of iminofuran: VIII. Recyclization of 5-aryl-3-arylimino-3H-furan-2-ones effected by cyanoacetic acid derivatives

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Abstract

The recyclization of 5-aryl-3-arylimino-3H-furan-2-ones under the action of esters, nitriles, and amides of cycnoacetic acids resulted in the corresponding esters, nitriles, and amides of (5E)-2-amino-1-aryl-4-oxo-5-(2-oxoethylidene)-1H-4,5-dihydropyrrole-3-carboxylic acids.

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Authors and Affiliations

  1. Perm State University, Perm, 614990, Russia

    S. S. Kharitonova & A. E. Rubtsov

  2. Perm State Pharmaceutical Academy, Perm, Russia

    N. M. Igidov & A. V. Zakhmatov

Authors
  1. S. S. Kharitonova
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  2. N. M. Igidov
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  3. A. V. Zakhmatov
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  4. A. E. Rubtsov
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Corresponding author

Correspondence to A. E. Rubtsov.

Additional information

Original English Text © S.S. Kharitonova, N.M. Igidov, A.V. Zakhmatov, A.E. Rubtsov, 2013, published in Zhurnal Organicheskoi Khimii, 2013, Vol. 49, No. 2, pp. 252–261.

For Communicacion VII, see [1].

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Kharitonova, S.S., Igidov, N.M., Zakhmatov, A.V. et al. Chemistry of iminofuran: VIII. Recyclization of 5-aryl-3-arylimino-3H-furan-2-ones effected by cyanoacetic acid derivatives. Russ J Org Chem 49, 243–252 (2013). https://doi.org/10.1134/S1070428013020115

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  • DOI: https://doi.org/10.1134/S1070428013020115

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