73721-27-4Relevant articles and documents
Pyridine-phosphinimine ligand-accelerated Cu(I)-catalyzed azide-alkyne cycloaddition for preparation of 1-(pyridin-2-yl)-1,2,3-triazole derivatives
Sun, Ranfeng,Wang, Huangdong,Hu, Jianfeng,Zhao, Jiudong,Zhang, Hao
, p. 5954 - 5963 (2014/08/05)
A series of phosphinimine ligands were designed and used in the Cu(i)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of tetrazolo[1,5-a]pyridines and alkynes for the first time. By optimizing the reaction conditions, an efficient catalytic system (CuCl/2-PyCH 2NPtBu3) was developed to give 1-(pyridin-2-yl)-1,2,3-triazole derivatives in moderate to excellent yields (46-98%). This journal is the Partner Organisations 2014.
Tetrazolopyridines and Furazanopyridine 1-Oxides
Lowe-Ma, Charlotte K.,Nissan, Robin A.,Wilson, William S.
, p. 3755 - 3761 (2007/10/02)
Tetrazolopyridines may be prepared by the reaction of azide ion with 2-chloropyridines.These tetrazolopyridines are shown to be in equilibrium with the corresponding 2-azidopyridines.Furazanopyridine 1-oxides may be prepared by thermolysis of the appropriate 4-nitrotetrazolopyridines, presumably via the corresponding 2-azido-3-nitropyridines.The furazanopyridine 1-oxides are found to be in equilibrium with the 3-oxides. 1H and 13C NMR are used to examine this equilibrium.