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Investigation of the reactivities and tautomerism of azolidines. 49. Synthesis of 4-thioxo-5-arylideneselenazolid-2-ones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A number of 5-benzylidene derivatives of 4-thioselenazolid-2-one with various substituents in the aromatic ring were synthesized as a result of the reaction of 4-thioxoselenazolid-2-one with aromatic aldehydes in acetic acid with 25% aqueous methylamine solution as the catalyst. The structure of the compounds was confirmed by alternative synthesis from the corresponding 5-arylideneselenazolidine-2,4-diones.

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Authors and Affiliations

  1. Lensovet Leningrad Technological Institute, 198013, Leningrad

    I. B. Levshin, K. A. V'yunov, A. A. Tsurkan, A. I. Ginak & N. L. Isaeva

  2. Academician I. P. Pavlov Ryazan Medical Institute, Ryazan

    I. B. Levshin, K. A. V'yunov, A. A. Tsurkan, A. I. Ginak & N. L. Isaeva

Authors
  1. I. B. Levshin
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  2. K. A. V'yunov
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  3. A. A. Tsurkan
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  4. A. I. Ginak
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  5. N. L. Isaeva
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Additional information

See [1] for communication 48.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 338–340, March, 1983.

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Levshin, I.B., V'yunov, K.A., Tsurkan, A.A. et al. Investigation of the reactivities and tautomerism of azolidines. 49. Synthesis of 4-thioxo-5-arylideneselenazolid-2-ones. Chem Heterocycl Compd 19, 273–275 (1983). https://doi.org/10.1007/BF00513258

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  • DOI: https://doi.org/10.1007/BF00513258

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