Abstract: | We have used 1H NMR to study the amine-imine tautomerism of some esters and amides of 2-N-labeled 4-methylthiazole-5-carboxylic acids and
5-carbamic acids. We have shown that the nature of the substituents of the 2-NHR1, 5-COR2, or 5-NHCOR2 groups affects that position of the tautomeric equilibrium.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1240–1243, August, 2005. |