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Asymmetric nitrogen. 57. Investigation of the stereochemistry of aziridinecarboxylic acid derivatives by NMR

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

The preferred trans configuration of 1,2-disubstituted aziridines and cis configuration of NH-aziridine-2-carboxylic esters were established by means of the1H and13C NMR spectra and the two-dimensional NOESY and COSY-45 spectra.

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Authors and Affiliations

  1. Institute of Chemical Physics, Academy of Sciences of the USSR, USSR

    I. I. Chervin, A. A. Fomichev, A. S. Moskalenko, N. L. Zaichenko, A. É. Aliev, A. V. Prosyanik, V. N. Voznesenskii & R. G. Kostyanovskii

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  1. I. I. Chervin
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  2. A. A. Fomichev
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  3. A. S. Moskalenko
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  4. N. L. Zaichenko
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  5. A. É. Aliev
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  6. A. V. Prosyanik
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  7. V. N. Voznesenskii
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  8. R. G. Kostyanovskii
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Additional information

For previous communications see [1].

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1110–1121, May, 1988.

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Chervin, I.I., Fomichev, A.A., Moskalenko, A.S. et al. Asymmetric nitrogen. 57. Investigation of the stereochemistry of aziridinecarboxylic acid derivatives by NMR. Russ Chem Bull 37, 972–982 (1988). https://doi.org/10.1007/BF00957072

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  • DOI: https://doi.org/10.1007/BF00957072

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