Recent advances in Cu-catalyzed carbonylation with CO

被引:13
|
作者
Yan, Xinlong [1 ]
Fan, Lin [1 ]
Zhang, Xiangdong [1 ]
Liu, Guodu [1 ]
机构
[1] Inner Mongolia Univ, Coll Chem & Chem Engn, Inner Mongolia Key Lab Fine Organ Synth, 24 Zhaojun Rd, Hohhot 010030, Peoples R China
基金
中国国家自然科学基金;
关键词
ARYLBORONIC ACIDS; C(SP(3))-H BONDS; N-CHLOROAMINES; HYDROFORMYLATION; COBALT; EFFICIENT; ANILINES; ALKYNES; AMIDES; ORGANOBORANES;
D O I
10.1039/d2qo01419j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition metal-catalyzed carbonylation has emerged as a powerful and versatile strategy for the efficient construction of complicated carbonyl-containing molecules from simple chemical feedstocks in the past decades. Although many transition metals, especially noble metals, such as Ru, Rh, Pd, and others, have been applied successfully for these transformations, non-noble metal Cu-catalyzed carbonylation has shown a lot of advantages in terms of its low cost and toxicity. In this review, recent advances and contributions in Cu-catalyzed carbonylation using CO as the C(1) source were summarized. A variety of easily accessible substrates were converted into valuable carbonylated products including ketones, esters, amides and other products. The synthetic strategies described in this review provided an alternative greener option for catalytic carbonylation. Further studies and developments in this field would be inspired in the future.
引用
收藏
页码:6749 / 6765
页数:17
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