Abstract
2-Phenylthiocarbamoylimino-3-aryl-4-oxothiazolidines, which are hydrolyzed at the C=N and N3=C4 bonds of the thiazolidine ring to give 3-arylthiazolidine-2,4-diones, N-phenylthiocarbamoylarylpseudothiohydantoic acids, and 3-phenylthiocarbamoylthiazolidine-2,4-dione, were synthesized by reaction of 2-imino-3-aryl-4-oxothiazolidines with phenyl isothiocyanate.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 903–905, July. 1976.
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Svetkin, Y.V., Vasil'eva, S.A. & Tokareva, L.D. Reaction of 2-imino-3-aryl-4-oxothiazolidines with phenyl isothiocyanate. Chem Heterocycl Compd 12, 751–753 (1976). https://doi.org/10.1007/BF00477004
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DOI: https://doi.org/10.1007/BF00477004