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

مؤلف البحث
A.M. Kamal El-Dean, A.A. Atalla b and A.M. Gaber
ملخص البحث

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.

قسم البحث
مجلة البحث
Journal of Analytical and Applied Pyrolysis
المشارك في البحث
الناشر
Elsevier Science Publishers B.V., Amsterdam
تصنيف البحث
1
عدد البحث
22
سنة البحث
1991
صفحات البحث
107-111