Abstract
The synthesis of 1-monosubstituted aryl 1,2,3-triazoles was achieved using calcium, carbide as a source of acetylene. The copper-catalyzed 1,3-dipolar cycloaddition reactions were carried out without nitrogen protection and in a MeCN - H2O mixture. The yields ranged from moderate to excellent. The reaction conditions were found to be successful for aryl azide reactants, including analogues with various functionalities.
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Jiang, Y., Kuang, C., & Yang, Q. (2009). The use of calcium carbide in the synthesis of 1-monosubstituted aryl 1,2,3-triazole via click chemistry. Synlett, (19), 3163–3166. https://doi.org/10.1055/s-0029-1218346
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