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

V. M. Berestovitskaya; R. I. Baichurin; N. I. Aboskalova; L. V. Baichurina; E. V. Trukhin; A. V. Fel’gendler; M. A. Gensirovskaya

doi:10.1134/S1070363216060086

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

Authors: Berestovitskaya V.M.¹, Baichurin R.I.¹, Aboskalova N.I.¹, Baichurina L.V.², Trukhin E.V.¹, Fel’gendler A.V.², Gensirovskaya M.A.¹
Affiliations:
1. Herzen State Pedagogical University of Russia
2. Kirov Military Medical Academy
Issue: Vol 86, No 6 (2016)
Pages: 1266-1273
Section: Article
URL: https://journals.rcsi.science/1070-3632/article/view/215228
DOI: https://doi.org/10.1134/S1070363216060086
ID: 215228

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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.