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Synthesis of 2,3-disubstituted thiazolidin-4-ones containing the sterically hindered 4-hydroxy-3,5-di(tert-butyl)phenyl grouping

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A series of 2,3-disubstituted thiazolidin-4-ones containing 4-hydroxy-3,5-di(tert-butyl)phenyl groups has been synthesized. For preparation of these sterically hindered compounds the condensation of thioglycolic acid with azomethines — derivatives of 4-hydroxy-3,5-di(tert-butyl)benzaldehyde was used.

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Authors
  1. M. A. Silin
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  2. V. I. Kelarev
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  3. V. Abu-Ammar
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Additional information

I. M. Gubkin Russian State University for Petroleum and Gas, Moscow 117917. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 256–260, February, 2000.

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Silin, M.A., Kelarev, V.I. & Abu-Ammar, V. Synthesis of 2,3-disubstituted thiazolidin-4-ones containing the sterically hindered 4-hydroxy-3,5-di(tert-butyl)phenyl grouping. Chem Heterocycl Compd 36, 214–218 (2000). https://doi.org/10.1007/BF02283555

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  • DOI: https://doi.org/10.1007/BF02283555

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