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Synthesis and ionization constants of 2-aryliminotetrahydrofurans

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The tetrafluoroborates of 2-aryliminotetrahydrofurans were synthesized by the reaction of 0-ethylbutyrolactonium tetrafluoroborate with aromatic amines, and a number of bases of imido esters with various substituents in the aromatic ring were synthesized by the reaction of aromatic amines with 2,2-diethoxytetrahydrofuran. The ionization constants of the products were measured.

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Authors and Affiliations

  1. S. Ozdzhonikidze All-Union Scientific-Research Institute of Pharmaceutical Chemistry, 119021, Moscow

    N. B. Marchenko, V. G. Granik, I. V. Persianova & R. G. Glushkov

Authors
  1. N. B. Marchenko
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  2. V. G. Granik
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  3. I. V. Persianova
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  4. R. G. Glushkov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 737–740, June, 1980.

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Marchenko, N.B., Granik, V.G., Persianova, I.V. et al. Synthesis and ionization constants of 2-aryliminotetrahydrofurans. Chem Heterocycl Compd 16, 565–568 (1980). https://doi.org/10.1007/PL00020438

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  • DOI: https://doi.org/10.1007/PL00020438

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