A series of diversely 1-substituted 4-amino 1,2,3-triazoles were synthesized by [3+2] cycloaddition between azides and ynamides. This copper catalyzed process represents the first examples of a 'click reaction' employing ynamides and should expand the scope of the ynamide chemistry both synthetically and industrially. Various azides (even highly functionalized) were allowed to react with N-benzyl, N-tosyl ynamide to give the corresponding triazole adducts in high yield and with very high levels of regioselectivity. © 2006 Elsevier Ltd. All rights reserved.
CITATION STYLE
IJsselstijn, M., & Cintrat, J. C. (2006). Click chemistry with ynamides. Tetrahedron, 62(16), 3837–3842. https://doi.org/10.1016/j.tet.2005.11.090
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