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2-Nitro-and 2-bromo-2-nitroethylphosphonates in the reaction with sodium azide

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Abstract

The reactions of phosphorylated 2-nitro-and 2-bromo-2-nitroethenes with sodium azide involve 1,3-dipolar cycloaddition to form triazoles, aziridines and isomeric vinyl azides. The latter products were isolated as a mixture of structural isomers. The structure of the obtained compounds was determined by IR and 1H and 31P NMR spectroscopy.

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Authors and Affiliations

  1. Gertsen Russian State Pedagogical University, nab. r. Moiki 48, St. Petersburg, 191186, Russia

    N. A. Anisimova, N. G. Makarova, G. A. Berkova & V. M. Berestovitskaya

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  1. N. A. Anisimova
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  2. N. G. Makarova
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  3. G. A. Berkova
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  4. V. M. Berestovitskaya
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Original Russian Text © N.A. Anisimova, N.G. Makarova, G.A. Berkova, V.M. Berestovitskaya, 2006, published in Zhurnal Obshchei Khimii, 2006, Vol. 76, No. 10, pp. 1612–1616.

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Anisimova, N.A., Makarova, N.G., Berkova, G.A. et al. 2-Nitro-and 2-bromo-2-nitroethylphosphonates in the reaction with sodium azide. Russ J Gen Chem 76, 1545–1549 (2006). https://doi.org/10.1134/S1070363206100069

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  • DOI: https://doi.org/10.1134/S1070363206100069

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