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Geminally activated nitroethenes in reactions with sodium azide. Synthesis of functionalized 1,2,3-triazoles

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Abstract

Reactions of geminally activated alkoxycarbonyl(acetyl, benzoyl, cyano)nitroethenes with sodium azide provided a series of functionally substituted 1,2,3-triazoles. Their structure was characterized by IR, 1H, and 13C–{1H} NMR spectroscopy.

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Correspondence to V. M. Berestovitskaya.

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Original Russian Text © V.M. Berestovitskaya, R.I. Baichurin, N.I. Aboskalova, L.V. Baichurina, E.V. Trukhin, A.V. Fel’gendler, M.A. Gensirovskaya, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 6, pp. 936–943.

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Berestovitskaya, V.M., Baichurin, R.I., Aboskalova, N.I. et al. Geminally activated nitroethenes in reactions with sodium azide. Synthesis of functionalized 1,2,3-triazoles. Russ J Gen Chem 86, 1266–1273 (2016). https://doi.org/10.1134/S1070363216060086

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