Diels-Alder Cycloaddition in Protein Chemistry

被引:40
作者
Palomo, Jose M. [1 ]
机构
[1] CSIC, Dept Biocatalisis, Inst Catalisis, Madrid 28049, Spain
关键词
Immobilization; Chemoselectivity; Cycloaddition; Biocatalysis; Chemical modification; Proteins; INVERSE-ELECTRON-DEMAND; SOLID-PHASE SYNTHESIS; CHEMICAL-MODIFICATION; IMMOBILIZATION STRATEGIES; SURFACE IMMOBILIZATION; RHODIUM CARBENOIDS; CATALYTIC ANTIBODY; DIRECTED EVOLUTION; ORGANIC-REACTIONS; STRUCTURAL BASIS;
D O I
10.1002/ejoc.201000859
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The Diels-Alder reaction is probably, together with aldol condensation, the most commonly used reaction in chemistry. The Diels-Alder approach, which involves a diene and a dienophile not present in any biomolecule, allows a chemo-selective reaction without the need of protecting groups. Moreover, water has an extraordinary rate-accelerating effect on the reaction process. Thus, this chemical approach has been recognized as a promising procedure for protein bioconjugation. In this review some of the most recent advances in the application of the Die Is-Alder reaction in selective surface modification, immobilization and biocatalysis will be discussed.
引用
收藏
页码:6303 / 6314
页数:12
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