Abstract
Hydroxymethylation and aminomethylation reactions of 5-arylidene-2-thio-4-oxazolidinones lead to the formation of substitution products at the ring nitrogen atom; this has been attributed to thermodynamic reaction control.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 106–108, January, 1989.
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Shenberg, N.A., Ginak, A.I., Ramsh, S.M. et al. 5-Arylidene-2-thio-4-oxazolidinones in hydroxy- and aminomethylation reactions. Chem Heterocycl Compd 25, 91–93 (1989). https://doi.org/10.1007/BF00472627
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DOI: https://doi.org/10.1007/BF00472627