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Investigation of the reactivities and tautomerism of azolidones. 52. Synthesis of 2- and 3-allyl-substituted pseudothiohydantoins

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The effect of the solvent on the cyclization of N-allylthiourea with monochloroacetic acid was studied; the structures of the products were proved by alternative synthesis, as well as by acidic hydrolysis.

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Authors and Affiliations

  1. Lensovet Leningrad Technological Institute, 198013, Leningrad

    I. B. Levshin, I. V. Grigor'eva, A. A. Tsurkan, É. L. Tarasyavichus, K. A. V'yunov & A. I. Ginak

  2. Academician I. P. Pavlov Ryazan Medical Institute, 390000, Ryazan

    I. B. Levshin, I. V. Grigor'eva, A. A. Tsurkan, É. L. Tarasyavichus, K. A. V'yunov & A. I. Ginak

Authors
  1. I. B. Levshin
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  2. I. V. Grigor'eva
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  3. A. A. Tsurkan
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  4. É. L. Tarasyavichus
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  5. K. A. V'yunov
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  6. A. I. Ginak
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Additional information

See [1] for Communication 51.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 336–338, March, 1985.

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Levshin, I.B., Grigor'eva, I.V., Tsurkan, A.A. et al. Investigation of the reactivities and tautomerism of azolidones. 52. Synthesis of 2- and 3-allyl-substituted pseudothiohydantoins. Chem Heterocycl Compd 21, 277–279 (1985). https://doi.org/10.1007/BF00506664

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  • DOI: https://doi.org/10.1007/BF00506664

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