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

作者: Berestovitskaya V.¹, Baichurin R.¹, Aboskalova N.¹, Baichurina L.², Trukhin E.¹, Fel’gendler A.², Gensirovskaya M.¹
隶属关系:
1. Herzen State Pedagogical University of Russia
2. Kirov Military Medical Academy
期: 卷 86, 编号 6 (2016)
页面: 1266-1273
栏目: Article
URL: https://journals.rcsi.science/1070-3632/article/view/215228
DOI: https://doi.org/10.1134/S1070363216060086
ID: 215228

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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.