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Synthesis and properties of heterocyclic analogs of isoflavones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The condensation of cyanomethyl derivatives of furan and benzofuran with di- and trihydric phenols has given the corresponding 2,4-dihydroxy- and 2,4,6-trihydroxy-α-heterylacetophenones. The latter have been converted by reaction with acid anhydride, ethoxalyl chloride, and trifluoroacetic anhydride into 3-heterylchromones with methyl, trifluoromethyl, and ethoxycarbonyl groups in position 2.

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Authors and Affiliations

  1. T. G. Shevchenko Kiev State University, USSR

    V. P. Khilya, L. G. Grishko, L. I. Shevchenko, L. I. Barvinok, V. A. Dymovich & V. Sabo

  2. L. Kossuth Debrecen University, USSR

    V. P. Khilya, L. G. Grishko, L. I. Shevchenko, L. I. Barvinok, V. A. Dymovich & V. Sabo

Authors
  1. V. P. Khilya
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  2. L. G. Grishko
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  3. L. I. Shevchenko
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  4. L. I. Barvinok
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  5. V. A. Dymovich
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  6. V. Sabo
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1202–1208, September, 1973.

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Khilya, V.P., Grishko, L.G., Shevchenko, L.I. et al. Synthesis and properties of heterocyclic analogs of isoflavones. Chem Heterocycl Compd 9, 1091–1097 (1973). https://doi.org/10.1007/BF00474779

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  • DOI: https://doi.org/10.1007/BF00474779

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