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Ammonolysis of aziridinecarboxylic acid esters

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The ammonolysis of 1-(2-methoxycarbonylvinyl)- and 1-(1,2-dimethoxycarbonylvinyl)-2-methoxycarbonylaziridines at normal pressure leads to 1-(2-methoxycarbonylvinyl)-and 1-(1,2-dicarbamoylvinyl)-2-carbamoylaziridines, respectively, whereas 1,3-diazabicyclo[3.1.0]hexan-4-one derivatives are formed under pressure.

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Literature cited

  1. I. Kalvins and E. B. Astapenok, Belgian Patent No. 860239; Chem. Abstr., 90, 34039 (1974).

    Google Scholar 

  2. K. Wüthrich, NMR in Biological Research: Peptides and Proteins, Elsevier, New York (1976), p. 177.

    Google Scholar 

  3. E. Kyburz, H. Els, St. Majnoni, G. Englert, C. V. Planta, and P. A. Plattner, Helv. Chim. Acta, 49, 359 (1966).

    Google Scholar 

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 350–352, March, 1983.

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Trapentsier, P.T., Kalvin'sh, I.Y., Liepin'sh, É.É. et al. Ammonolysis of aziridinecarboxylic acid esters. Chem Heterocycl Compd 19, 283–285 (1983). https://doi.org/10.1007/BF00513260

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  • DOI: https://doi.org/10.1007/BF00513260

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