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Absolute configuration of diastereomeric derivatives of N-substituted aziridine-2-carboxylic acids

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Individual diastereomers of a number of anilides of N-substituted aziridine-2-carboxylic acids have been obtained. Conclusions regarding the spatial structure of the compounds indicated have been drawn on the basis of the 1H NMR, 15N NMR, and CD spectra.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, 226006, Riga

    A. V. Eremeev, F. D. Polyak, I. A. Vosekalna, I. I. Chervin, Sh. S. Nasibov & R. G. Kostyanovskii

  2. Institute of Chemical Physics, Academy of Sciences of the USSR, 117334, Moscow

    A. V. Eremeev, F. D. Polyak, I. A. Vosekalna, I. I. Chervin, Sh. S. Nasibov & R. G. Kostyanovskii

Authors
  1. A. V. Eremeev
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  2. F. D. Polyak
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  3. I. A. Vosekalna
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  4. I. I. Chervin
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  5. Sh. S. Nasibov
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  6. R. G. Kostyanovskii
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Additional information

Report 37 of the series entitled “Asymmetric nonbridging nitrogen.” For report 36 see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1343–1348, October, 1984.

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Eremeev, A.V., Polyak, F.D., Vosekalna, I.A. et al. Absolute configuration of diastereomeric derivatives of N-substituted aziridine-2-carboxylic acids. Chem Heterocycl Compd 20, 1102–1107 (1984). https://doi.org/10.1007/BF00503598

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  • DOI: https://doi.org/10.1007/BF00503598

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