SYNTHESIS OF 2,3-DISUBSTITUTED THIAZOLIDIN-4-ONES CONTAINING THE STERICALLY HINDERED 4-HYDROXY-3,5-DI(<i>tert</i>-BUTYL)PHENYL GROUPING

Authors

  • М. А. Силин I. M. Gubkin Russian State University for Petroleum and Gas, Moscow
  • В. И. Келарев I. M. Gubkin Russian State University for Petroleum and Gas, Moscow
  • В. Абу-Аммар I. M. Gubkin Russian State University for Petroleum and Gas, Moscow

DOI:

https://doi.org/10.1007/56

Keywords:

azomethines, thiazolidine, thioglycolic acid, phenols, condensation

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.

Authors: M. A. Silin, V. I. Kelarev, and V. Abu-Ammar.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (2), pp 214-218

http://link.springer.com/article/10.1007/BF02283555

Published

2012-11-16

Issue

Section

Original Papers