SYNTHESIS OF 2,3-DISUBSTITUTED THIAZOLIDIN-4-ONES CONTAINING THE STERICALLY HINDERED 4-HYDROXY-3,5-DI(<i>tert</i>-BUTYL)PHENYL GROUPING
DOI:
https://doi.org/10.1007/56Keywords:
azomethines, thiazolidine, thioglycolic acid, phenols, condensationAbstract
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