Abstract
Micellar media in water provide a simple and efficient environment favoring the multi-component synthesis of 1,2,3-triazoles from organic bromides, sodium azide and terminal alkynes in the presence of [Cu(IMes)Cl] 1 catalyst at room temperature within a few hours. The micellar medium favors both the in situ formation of the organic azide and its metal promoted cycloaddition with the alkyne. This journal is
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CITATION STYLE
Tasca, E., La Sorella, G., Sperni, L., Strukul, G., & Scarso, A. (2015). Micellar promoted multi-component synthesis of 1,2,3-triazoles in water at room temperature. Green Chemistry, 17(3), 1414–1422. https://doi.org/10.1039/c4gc02248c
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