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Study of the tautomerism of acetyl- and carbethoxy-substituted tetrahydrofuranones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The equilibrium position of 2-methyl-4-cartaethoxytetrahydro-3-furanone, 2-methyl-4,5-dicarbethoxytetrahydro-3-furanone, and 3-acetyltetrahydro-2-furanone in acetonitrile, dioxane, and alcohols was determined. It was shown that the two Meyer equations are satisfied for these keto-enols paired with acetylacetone.

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Academy of Sciences of the USSR, Kazan

    O. A. Erastov, S. N. Ignat'eva & T. V. Malkova

Authors
  1. O. A. Erastov
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  2. S. N. Ignat'eva
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  3. T. V. Malkova
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1313–1319, October, 1971.

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Erastov, O.A., Ignat'eva, S.N. & Malkova, T.V. Study of the tautomerism of acetyl- and carbethoxy-substituted tetrahydrofuranones. Chem Heterocycl Compd 7, 1227–1232 (1971). https://doi.org/10.1007/BF00479936

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  • DOI: https://doi.org/10.1007/BF00479936

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