Abstract
In all cases the cyanoethylation, carbomethoxyethylation, and methylation of 2-amino(imino)thiazoli(di)ne derivatives that are substituted at the exocyclic nitrogen atom lead to the simultaneous formation of isomeric products with 2-iminothiazolidine and 2-amino-δ2-thiazoline structures.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 563–566, April, 1990.
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Mizrakh, L.I., Polonskaya, L.Y., Gvozdetskii, A.N. et al. Reactions of 2-iminothiazolidine derivatives with acrylonitrile, methyl acrylate, and methyl iodide. Chem Heterocycl Compd 26, 482–485 (1990). https://doi.org/10.1007/BF00497227
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DOI: https://doi.org/10.1007/BF00497227