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Ethyleneimine chemistry

VII. Synthesis and properties of 2-alkyl-substituted 1,3-diazabicyclo[3.1.0]hexanes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The previously unknown 2-alkyl-substituted 1,3-diazabicyclo[3.1.0]hexanes are formed as the major products in the reactions of C-aminomethylethyleneimine with aldehydes and ketones. Their structures were proved by IR and PMR spectroscopy.

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Literature cited

  1. M. Yu. Lidak and S. A. Giller, Izv. Akad. Nauk Latv.SSR, No. 5, 99 (1961).

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the LatvianSSR, Riga

    S. A. Giller, A. V. Eremeev, M. Yu. Lidak, V. A. Kholodnikov & V. A. Pestunovich

Authors
  1. S. A. Giller
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  2. A. V. Eremeev
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  3. M. Yu. Lidak
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  4. V. A. Kholodnikov
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  5. V. A. Pestunovich
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 607–609, May, 1971.

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Giller, S.A., Eremeev, A.V., Lidak, M.Y. et al. Ethyleneimine chemistry. Chem Heterocycl Compd 7, 567–569 (1971). https://doi.org/10.1007/BF00945493

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  • DOI: https://doi.org/10.1007/BF00945493

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