Metal-catalyzed azide-alkyne "click" reactions: Mechanistic overview and recent trends

被引:268
|
作者
Wang, Changlong [1 ]
Ikhlef, Djamila [2 ,3 ]
Kahlal, Samia [2 ]
Saillard, Jean-Yves [2 ]
Astruc, Didier [1 ]
机构
[1] Univ Bordeaux, CNRS, ISM, UMR 5255, F-33405 Talence, France
[2] Univ Rennes 1, CNRS, ISCR, UMR 6226, F-35042 Rennes, France
[3] Univ Sci & Technol Houari Boumedienne, Lab Physicochim Theor & Chim Informat, BP 32, El Alia, Alger, Algeria
关键词
Metal-Catalyzed Alkyne-Azide; Cycloaddition; Copper; Click; Mechanism; CuAAC; ONE-POT SYNTHESIS; N-HETEROCYCLIC CARBENE; MICROWAVE-ASSISTED SYNTHESIS; HIGHLY EFFICIENT; 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES; 1,3-DIPOLAR CYCLOADDITION; REUSABLE CATALYST; HETEROGENEOUS CATALYST; COPPER NANOPARTICLES; TERMINAL ALKYNES;
D O I
10.1016/j.ccr.2016.02.010
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This review is focused on the mechanistic aspects and recent trends of the metal -catalyzed azide-alkyne cycloaddition (MAAC) so-called "click" reactions with catalysts based on various metals (Cu, Ru, Ag, Au, Ir, Ni, Zn, Ln), although Cu (I) catalysts are still the most used ones. These MAAC reactions are by far the most common click reactions relevant to the "green chemistry" concept. First developed by the FokinSharpless and Meldal group with Cu(I) in 2002, they have then been extended to Ru(II) catalysts by the Fokin group in 2005 and finally to many other metal catalysts. Mechanistic investigations are essential to reaction improvements and subsequent applications, and indeed as shown in this review the proposed mechanisms have been multiple during the last decade based on theoretical computations and experimental search of intermediates. New trends (since 2012) are also presented here often representing both exciting approaches for various applications and new challenges for further mechanistic investigations. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 20
页数:20
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