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Ring opening in 5-aryl-2,3-furandiones synthesis of aroylpyruvic acid esters

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Aroylpyruvic acid esters are formed by the action of alcohols and phenol on 5-aryl-2,3-furandiones.

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Literature cited

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Authors and Affiliations

  1. Perm Pharmaceutical Institute, 614600, Perm

    Yu. S. Andreichikov, S. P. Tendryakova, Yu. A. Nalimova & G. D. Plakhina

Authors
  1. Yu. S. Andreichikov
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  2. S. P. Tendryakova
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  3. Yu. A. Nalimova
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  4. G. D. Plakhina
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Additional information

Communication III from the series “Chemistry of Oxalyl Derivatives of Methyl Ketones.” See [1] for communication II.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1030–1031, August, 1977.

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Andreichikov, Y.S., Tendryakova, S.P., Nalimova, Y.A. et al. Ring opening in 5-aryl-2,3-furandiones synthesis of aroylpyruvic acid esters. Chem Heterocycl Compd 13, 826–827 (1977). https://doi.org/10.1007/BF00488899

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  • DOI: https://doi.org/10.1007/BF00488899

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