Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleGeminally activated nitroethenes in reactions with sodium azide. Synthesis of functionalized 1,2,3-triazoles.AuthorsBerestovitskaya, V.; Baichurin, R.; Aboskalova, N.; Baichurina, L.; Trukhin, E.; Fel'gendler, A.; Gensirovskaya, M.AbstractReactions 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, H, and C-{H} NMR spectroscopy.SubjectsNITROETHYLENE; SODIUM azide; TRIAZOLES synthesis; CARBONYL compounds; NUCLEAR magnetic resonance spectroscopyPublicationRussian Journal of General Chemistry, 2016, Vol 86, Issue 6, p1266ISSN1070-3632Publication typeArticleDOI10.1134/S1070363216060086