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5-Arylfuran-2,3-diones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

5-Arylfuran-2,3-diones were obtained by cyclization of aroylpyruvic acids in the presence of thionyl chloride. It is shown that the five-membered ring of 5-arylfuran-2,3-diones is unstable and is cleaved under mild conditions under the influence of nucleophilic reagents.

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Literature cited

  1. E. Ziegler, M. Eder, C. Belegratis, and E. Prewedourakis, Monatsh. Chem., 98, 2249 (1967).

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  2. L. A. Kazitsina and N. B. Kuplet-skaya, Application of UV, IR, and NMR Spectroscopy in Organic Chemistry [in Russian], Moscow (1971), p. 244.

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Authors and Affiliations

  1. Perm Pharmaceutical Institute, USSR

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

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

Communication I from the series “Chemistry of Oxalyl Derivatives of Methyl Ketones.”

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1468–1470, November, 1975.

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Andreichikov, Y.S., Nalimova, Y.A., Plakhina, G.D. et al. 5-Arylfuran-2,3-diones. Chem Heterocycl Compd 11, 1252–1254 (1975). https://doi.org/10.1007/BF00474446

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  • DOI: https://doi.org/10.1007/BF00474446

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