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1-Alkoxyaziridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding 1-alkoxyaziridines were synthesized by oxidation of methoxy-, ethoxy-, and isopropoxyamines with lead tetraacetate in the presence of 2-methyl-2-butene and 2,3-dimethyl-2-butene. The PMR spectra of the oxidation products were investigated, and the high pyramidal stability of nitrogen in these compounds was confirmed. The individual invertomers 1-alkoxy-2,2,3-trimethylaziridines were isolated by preparative gas-liquid chromatography.

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Authors and Affiliations

  1. Leningrad State University, USSR

    B. V. Ioffe & E. V. Koroleva

Authors
  1. B. V. Ioffe
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  2. E. V. Koroleva
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1514–1519, November, 1972.

The authors thank A. A. Potekhin, I. N. Somin, R. R. Kostikov, M. I. Komendantov, and M. A. Kuznetsov for their useful discussions.

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Ioffe, B.V., Koroleva, E.V. 1-Alkoxyaziridines. Chem Heterocycl Compd 8, 1367–1371 (1972). https://doi.org/10.1007/BF00471872

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  • DOI: https://doi.org/10.1007/BF00471872

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