Copper catalysis with redox-active ligands

被引:23
|
作者
Das, Agnideep [1 ]
Ren, Yufeng [2 ]
Hessin, Cheriehan [1 ]
Desage-El Murr, Marine [1 ]
机构
[1] Univ Strasbourg, Inst Chim, UMR CNRS 7177, Strasbourg 67000, France
[2] Sorbonne Univ, Inst Parisien Chim Mol, UMR CNRS 8232, Paris 75005, France
来源
关键词
bioinspired catalysis; biomimetic copper complexes; cooperative catalysis; redox-active ligands; redox catalysis; AEROBIC OXIDATION; GALACTOSE-OXIDASE; COMPLEXES; AZIRIDINATION; HYDROXYLATION; RADICALS; MODELS; SYSTEM; STATES; CU;
D O I
10.3762/bjoc.16.77
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphines and N-heterocyclic carbenes, a new and fast-expanding area of research is exploring the possibility of a complementing metal-centered reactivity with electronic participation by the coordination sphere. To achieve this electronic flexibility, redox-active ligands can be used to engage in a fruitful "electronic dialogue" with the metal center, and provide additional venues for electron transfer. This review aims to present the latest results in the area of copper-based cooperative catalysis with redox-active ligands.
引用
收藏
页码:858 / 870
页数:13
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