Abstract
Macrocyclic phthalic acid diamides were obtained by the reaction of N,N′-substituted diphthalimides with polyoxyethylenediamines, while the corresponding tetraamides were obtained with primary aliphatic amines. It is shown that the reaction is a thermodynamically controlled process.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 246–249, February, 1982.
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Anikin, V.F., Ganin, É.V., Rozynov, B.V. et al. Peculiarities of the reaction of N,N′-substituted diphthalimides with amines. Chem Heterocycl Compd 18, 193–196 (1982). https://doi.org/10.1007/BF00512968
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DOI: https://doi.org/10.1007/BF00512968