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Molecular rearrangements of sulphur compounds
Part 3. Pyrolysis of substituted thiazolidinones

Research Abstract
Pyrolysis of 2-arylimino-3-arylthiazolidin-4-one gives rise to water, aniline, acetanilide, azobenzene, benzonitrile, p-toluonitrile, indole, benzthiazole, 6-methylbenzthiazole, thioglycolic acid, phenylisothiocyanate, p-tolylisothiocyanate, thiocarbanilide, N-phenyl-N-ptolylthiourea, p-aminoacetophenone and N-phenylbenzimidazole. A free radical mechanism has been suggested to account for the formation of the products.
Research Authors
A.M. Kamal El-Dean, A.A. Atalla b and A.M. Gaber
Research Department
Research Journal
Journal of Analytical and Applied Pyrolysis
Research Pages
107-111
Research Publisher
Elsevier Science Publishers B.V., Amsterdam
Research Rank
1
Research Vol
22
Research Year
1991