Abstract
For the first time, the sulfur heteroatom of 4-oxothiazolidines has been iminated with sodium salts of chloroamides of arenesulfonic acids and N-chloroamides of carboxylic acids. The effect of the substituents and the size of the ring on the ability of the ring sulfur atom to undergo oxidative imination was studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 609–612, May, 1979.
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Gontar', S.S., Druzhinina, G.I., Kremlev, M.M. et al. Oxidative imination of sulfur-containing heterocycles. Chem Heterocycl Compd 15, 493–495 (1979). https://doi.org/10.1007/BF00773212
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DOI: https://doi.org/10.1007/BF00773212