Abstract
Alkyl(aryl)benzazolylazoketoximes were obtained by nitrosation of the hydrazones of alkyl- and aryl-substituted aldehydes by means of n-amyl nitrite. On the basis of data from IR and PMR spectroscopy it was concluded that the synthesized compounds exist in the oxime form. Their acid ionization constants were determined.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1101–1105, August, 1980.
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Medvedeva, L.I., Lipunova, G.N., Bednyagina, N.P. et al. Synthesis and structures of alkyl (aryl) benzazolylazoketoximes. Chem Heterocycl Compd 16, 857–860 (1980). https://doi.org/10.1007/BF00513171
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DOI: https://doi.org/10.1007/BF00513171