CuAAC: An Efficient Click Chemistry Reaction on Solid Phase

被引:176
|
作者
Castro, Vida [1 ,2 ]
Rodriguez, Hortensia [1 ,2 ,4 ]
Abericio, Fernando [1 ,2 ,3 ,5 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Res Biomed IRE Barcelona, Barcelona 08028, Spain
[2] CIBER BBN, Networking Ctr Bioengn Biomat & Nanomed, Barcelona 08028, Spain
[3] Univ Barcelona, Dept Organ Chem, E-08028 Barcelona, Spain
[4] Yachay City Knowledge, Yachay Tech, Sch Chem, Urcuqui, Ecuador
[5] Univ KwaZulu Natal, Sch Chem & Phys, Durban 4001, South Africa
关键词
Click Chemistry; CuAAC; solid-phase; azide; alkyne; AZIDE-ALKYNE CYCLOADDITION; DIAZO-TRANSFER REACTION; IMIDAZOLE-1-SULFONYL AZIDE; PARALLEL SYNTHESIS; 1,3-DIPOLAR CYCLOADDITIONS; CATALYTIC DIAZOTRANSFER; AUTOMATED SYNTHESIS; SUPPORTED SYNTHESIS; GALACTOSYL CLUSTER; ORGANIC-CHEMISTRY;
D O I
10.1021/acscombsci.5b00087
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Click chemistry is an approach that uses efficient and reliable reactions, such as Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), to bind two molecular building blocks. CuAAC has broad applications in medicinal chemistry and other fields of chemistry. This review describes the general features and applications Of CuAAC in solid-phase synthesis (CuAAC-SP), highlighting the suitability of this kind of reaction for peptides, nucleotides, small molecules, supramolecular structures, and polymers, among others. This versatile reaction is expected to become pivotal for meeting future challenges in solid-phase chemistty.
引用
收藏
页码:1 / 14
页数:14
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