Dirhodium: carbene transformations and beyond

被引:18
|
作者
Wu, Rui [1 ]
Zhu, Dong [1 ]
Zhu, Shifa [1 ,2 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510640, Peoples R China
[2] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
基金
中国博士后科学基金;
关键词
C-H ACTIVATION; DIELS-ALDER REACTIONS; CHIRAL LEWIS-ACID; PERFLUOROBUTYRATE CATALYZED HYDROSILYLATION; INSERTION REACTIONS; SKELETAL REORGANIZATION; ASYMMETRIC-SYNTHESIS; RHODIUM(II) ACETATE; ARYLBORONIC ACIDS; ALLYLIC OXIDATION;
D O I
10.1039/d3qo00400g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dirhodiums, which feature lantern- or paddlewheel-like structures, have emerged as a class of useful catalysts in organic synthesis. Among the transformations catalyzed by dirhodiums, the carbene, with diazo, cyclopropene, hydrazone and triazole as the precursors, and nitrene transfer reactions are dominant and have reached remarkable levels of efficiency and selectivity. Additionally, more and more fascinating properties of dirhodium have been explored and discovered in the past few decades, which has accelerated the applications of dirhodium in organic synthesis. In this review, we aim to showcase these advances in dirhodium-catalyzed transformations. The transformations including cycloisomerization, hetero-Diels-Alder (HDA) reactions, ene reactions, arylation, radical oxidation reactions and C-H activation, etc. will be covered. In these reactions, the dirhodiums could not only work as redox-neutral catalysts but also as redox catalysts.
引用
收藏
页码:2849 / 2878
页数:30
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