Click chemistry under non-classical reaction conditions

被引:370
作者
Kappe, C. Oliver [1 ,2 ]
Van der Eycken, Erik [3 ]
机构
[1] Karl Franzens Univ Graz, CDLMC, A-8010 Graz, Austria
[2] Karl Franzens Univ Graz, Inst Chem, A-8010 Graz, Austria
[3] Katholieke Univ Leuven, Dept Chem, Lab Organ & Microwave Assisted Chem, B-3001 Louvain, Belgium
关键词
AZIDE-ALKYNE CYCLOADDITION; MICROWAVE-ASSISTED SYNTHESIS; MODULAR FLOW REACTOR; 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES; 1,3-DIPOLAR CYCLOADDITION; EFFICIENT SYNTHESIS; IONIC LIQUIDS; OLIGONUCLEOTIDES; TRIAZOLES; SYSTEM;
D O I
10.1039/b901973c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
First described almost a decade ago, "click'' reactions such as the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) are widely used today in organic and medicinal chemistry, in the polymer and material science field, and in chemical biology. While most click reactions can be performed at room temperature there are instances where some form of process intensification is required. In this tutorial review, aimed at the synthetic chemistry community, examples of click chemistry carried out under non-classical reaction conditions, such as for example applying microwave heating or continuous flow processing will be highlighted.
引用
收藏
页码:1280 / 1290
页数:11
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