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Giorgioni, G., Claudi, F., Ruggieri, S., Ricciutelli, M., Palmieri, G.F., Di-Stefano, A., Sozio, P., Cerasa, L.S., Chiavaroli, A., Ferrante, C., Orlando and G., Glennon, (2010) Design, synthesis, and preliminary pharmacological evaluation of new imidazolinones as l-DOPA prodrugs. Bioorganic & Medicinal Chemistry Letters, 18, 1834-1843. doi:10.1016/j.bmc.2010.01.041

has been cited by the following article:

• TITLE: Reaction of thiocarboxanilide derivatives of 2-phenylimino-3-phenyl-4-thiazolidinone and 1,3-diphenyl-2-thioxo-4-imidazolone with hydrazonoyl halides and active chloromethylene compounds

  AUTHORS: Hamdi M. Hassaneen, Omar A. Miqdad, Nada M. Abunada, Ahmad A. Fares

  KEYWORDS: Hydrazonoyl Halides; 1, 3, 4-Thiadiazoline; Thiazolidinone

  JOURNAL NAME: Natural Science, Vol.3 No.3, March 31, 2011

  ABSTRACT: The potassium salts of thiocarboxanilide of 2- phenylimino-3-phenyl-4-thiazolidinone and 1,3- diphenyl-2-thioxo-4-imidazolone react with hydrazonoyl halides in N,N-dimethylformamide to afford the corresponding 1,3,4-thiadiazoline derivatives. 2-Phenylimino-3-phenyl-4-thiazolidinone reacts with active chloromethylene compounds in N,N-dimethylformamide to give the corresponding thiazolylidenethiazolidin-4-one derivatives. The new compounds were characterized using IR, 1H NMR, 13C NMR and mass spectra.