Abstract
2-Acylimino-1,3,4-thiadiazoles were obtained from 1-methyl-1-thioacylhydrazines and the appropriate acyl isothiocyanates, while 2-benzoylimino-1,3,4-oxadiazole was obtained from 1-phenyl-1-benzoylhydrazine and benzoyliminocarbonic acid dichloride. The mesoionic structure of the compounds obtained was proved by their IR and mass spectra. Reduction, hydrolysis, and salt-formation reactions of them were studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1345–1350, October, 1973.
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Lazaris, A.Y., Shmuilovich, S.M. & Egorochkin, A.N. Mesoionic 2-acylimino-1,3,4-thia- and -oxadiazoles. Chem Heterocycl Compd 9, 1216–1221 (1973). https://doi.org/10.1007/BF00477454
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DOI: https://doi.org/10.1007/BF00477454