Covalent Cages with Inwardly Directed Reactive Centers as Confined Metal and Organocatalysts

被引:15
|
作者
Yang, Jian [1 ]
Chatelet, Bastien [1 ]
Herault, Damien [1 ]
Dutasta, Jean-Pierre [2 ]
Martinez, Alexandre [1 ]
机构
[1] Aix Marseille Univ, CNRS, Cent Marseille, ISm2,UMR 7313, F-13397 Marseille, France
[2] UCBL, CNRS, Ecole Normale Super Lyon, Lab Chim, F-69364 Lyon, France
关键词
Supramolecular chemistry; Cage compounds; Organocatalysis; Metal catalysts; Host-guest systems; DIELS-ALDER REACTIONS; SUPRAMOLECULAR CATALYSIS; CAPPED CYCLODEXTRINS; ESTER HYDROLYSIS; HEMICRYPTOPHANE; COMPLEXES; RECOGNITION; CHEMISTRY; STABILIZATION; CALIXARENES;
D O I
10.1002/ejoc.201800867
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Covalent cages with a well-defined cavity located close to a reactive center are of increasing interest because of their outstanding ability to mimic the catalytic properties of enzymatic systems. The size and shape of such synthetic nanosized reactors strongly affect the behavior of the trapped reaction partners, which can adopt specific conformations and orientations. In particular, the use of molecular cages with confined reactive functions strongly modifies the outcome of catalytic transformations that are carried out therein. This review article describes covalent molecular cages presenting an endohedral functionalization of their inner space and reports on their catalytic activities compared with those of model systems that lack cavity.
引用
收藏
页码:5618 / 5628
页数:11
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