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

被引:269
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
相关论文
共 262 条
[1]   Spatial and temporal control of the alkyne-azide cycloaddition by photoinitiated Cu(II) reduction [J].
Adzima, Brian J. ;
Tao, Youhua ;
Kloxin, Christopher J. ;
DeForest, Cole A. ;
Anseth, Kristi S. ;
Bowman, Christopher N. .
NATURE CHEMISTRY, 2011, 3 (03) :256-259
[2]   Click Chemistry: 1,2,3-Triazoles as Pharmacophores [J].
Agalave, Sandip G. ;
Maujan, Suleman R. ;
Pore, Vandana S. .
CHEMISTRY-AN ASIAN JOURNAL, 2011, 6 (10) :2696-2718
[3]   Enhanced reactivity of dinuclear Copper(I) acetylides in dipolar cycloadditions [J].
Ahlquist, Marten ;
Fokin, Valery V. .
ORGANOMETALLICS, 2007, 26 (18) :4389-4391
[4]   AgN(CN)2/DIPEA/H2O-EG: a highly efficient catalytic system for synthesis of 1,4-disubstituted-1,2,3 triazoles at room temperature [J].
Ali, Abdul Aziz ;
Chetia, Mitali ;
Saikia, Bishwajit ;
Saikia, Prakash J. ;
Sarma, Diganta .
TETRAHEDRON LETTERS, 2015, 56 (43) :5892-5895
[5]   Copper Nanoparticles in Click Chemistry [J].
Alonso, Francisco ;
Moglie, Yanina ;
Radivoy, Gabriel .
ACCOUNTS OF CHEMICAL RESEARCH, 2015, 48 (09) :2516-2528
[6]   Alkenes as Azido Precursors for the One-Pot Synthesis of 1,2,3-Triazoles Catalyzed by Copper Nanoparticles on Activated Carbon [J].
Alonso, Francisco ;
Moglie, Yanina ;
Radivoy, Gabriel ;
Yus, Miguel .
JOURNAL OF ORGANIC CHEMISTRY, 2013, 78 (10) :5031-5037
[7]   Unsupported Copper Nanoparticles in the 1,3-Dipolar Cycloaddition of Terminal Alkynes and Azides [J].
Alonso, Francisco ;
Moglie, Yanina ;
Radivoy, Gabriel ;
Yus, Miguel .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 2010 (10) :1875-1884
[8]   Evaluation and development of novel photoinitiator complexes for photoinitiating the copper-catalyzed azide-alkyne cycloaddition reaction [J].
Alzahrani, Abeer A. ;
Erbse, Annette H. ;
Bowman, Christopher N. .
POLYMER CHEMISTRY, 2014, 5 (06) :1874-1882
[9]   A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction [J].
Appukkuttan, P ;
Dehaen, W ;
Fokin, VV ;
Van der Eycken, E .
ORGANIC LETTERS, 2004, 6 (23) :4223-4225
[10]   Recent Advances in Click Chemistry Applied to Dendrimer Synthesis [J].
Arseneault, Mathieu ;
Wafer, Caroline ;
Morin, Jean-Francois .
MOLECULES, 2015, 20 (05) :9263-9294