CO2= CO + [O]: recent advances in carbonylation of C-H bonds with CO2

被引:110
作者
Song, Lei [1 ]
Jiang, Yuan-Xu [1 ]
Zhang, Zhen [1 ,2 ]
Gui, Yong-Yuan [1 ,3 ]
Zhou, Xiao-Yu [1 ]
Yu, Da-Gang [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Peoples R China
[2] Chengdu Univ, Coll Pharm & Biol Engn, Chengdu 610106, Peoples R China
[3] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610068, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSITION-METAL-FREE; CATALYZED OXIDATIVE CARBONYLATION; H BONDS; C(SP(3))-H BONDS; DIRECT CARBOXYLATION; SITE-SELECTIVITY; RECENT PROGRESS; CARBON-DIOXIDE; DERIVATIVES; DESIGN;
D O I
10.1039/d0cc00547a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon dioxide (CO2) is an ideal one-carbon source owing to its nontoxicity, abundance, availability, and recyclability. Although the thermodynamic stability and kinetic inertness of CO(2)bring its utilization challenges, many groups have achieved significant progress in the utilization of CO(2)to synthesize valuable carbonyl-containing compounds, which could be also generatedviaoxidative carbonylation of C-H bonds with CO. As CO(2)has a higher oxidation state than CO, it could be considered as a combination of CO and oxidant (CO2= CO + [O]), thus providing a safe, redox-neutral and economic strategy. In this Feature Article, we have summarized the recent advances in carbonylation of C-H bonds with CO(2)based on this concept. The plausible mechanisms of such reactions and future of this field are also discussed.
引用
收藏
页码:8355 / 8367
页数:13
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