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Investigation of the direction of enolization of some furyl-substituted β-diketones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It was found that ω-benzoyl-2-acetyl-, ω-benzoyl-2-acetyl-5-bromo-, ω-(2-thenoyl-2-acetyl-, and ω-(5-bromo-2-thenoyl)-2-acetyl-bromofurans are enolized at the carbonyl group in the α position relative to the furyl grouping.

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Authors and Affiliations

  1. Institute of Chemistry, N. Kopernik University, Torun, Poland

    T. Lesiak & S. Nielek

Authors
  1. T. Lesiak
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  2. S. Nielek
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 162–166, February, 1975.

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Lesiak, T., Nielek, S. Investigation of the direction of enolization of some furyl-substituted β-diketones. Chem Heterocycl Compd 11, 137–140 (1975). https://doi.org/10.1007/BF00471382

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  • DOI: https://doi.org/10.1007/BF00471382

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