Abstract
A mixture of cis- and trans-4-alkyl(heteryl, aryl)aminothiolan-3-ol 1,1-dioxides and (3-hydroxy-1,1-dioxothiolan-4-ylamino)acetic acids have been obtained by the reaction of 2,3-dihydrothiophene-3-ol 1,1-dioxide with aliphatic, heterocyclic, and aromatic amines and aminoacetic acid. The structures of the compounds isolated has been shown by chemical and spectral methods.
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Translated from Khimiya Geterotskiklicheskikh Soedinenii, No. 4, pp. 475–478, April, 1980.
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Bezmenova, T.É., Dul'nev, P.G. & Rybakova, M.V. A study of the conditions of the formation of the cis and trans isomers of N-substituted 4-aminothiolan-3-ol 1,1-dioxides. Chem Heterocycl Compd 16, 359–362 (1980). https://doi.org/10.1007/BF00552774
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DOI: https://doi.org/10.1007/BF00552774