The First Well??Defined Silver (I)??Complex??Catalyzed Cycloaddition of Azides onto Terminal Alkynes at Room Temperature
J McNulty, K Keskar, R Vemula
Index: McNulty, James; Keskar, Kunal; Vemula, Ramesh Chemistry - A European Journal, 2011 , vol. 17, # 52 p. 14727 - 14730
Full Text: HTML
Citation Number: 64
Abstract
The copper (I)-catalyzed Huisgen dipolar cycloaddition of terminal alkynes 1 with azides 2 [1] to yield 1, 4-and 1, 4, 5-substituted 1, 2, 3-triazoles 3 (azide–alkyne cycloaddition; AAC reaction) has been transformed in recent years, since its description as the prototype “click” reaction,[2] to become a general process with applications in diverse areas ranging from functional materials [3] to biological chemistry.[4, 5] The generally accepted mechanism ...
Related Articles:
Copper (I)-doped Wyoming's montmorillonite for the synthesis of disubstituted 1, 2, 3-triazoles
[Jlalia, Ibtissem; Elamari, Hichem; Meganem, Faouzi; Herscovici, Jean; Girard, Christian Tetrahedron Letters, 2008 , vol. 49, # 48 p. 6756 - 6758]
Porous copper catalyzed click reaction in water
[Zhang, Chen; Huang, Bo; Chen, Ying; Cui, Dong-Mei New Journal of Chemistry, 2013 , vol. 37, # 9 p. 2606 - 2609]
[bmim] BF 4/[Cu (Im 12) 2] CuCl 2 as a novel catalytic reaction medium for click cyclization
[Keshavarz, Mosadegh; Karami, Bahador; Ahmady, Amanollah Zarei; Ghaedi, Abdolmohammad; Vafaei, Hakimeh Comptes Rendus Chimie, 2014 , vol. 17, # 6 p. 570 - 576]