Selective Decarbonylation via Transition-Metal-Catalyzed Carbon- Carbon Bond Cleavage

被引:175
|
作者
Lu, Hong [1 ]
Yu, Tian-Yang [1 ]
Xu, Peng-Fei [2 ]
Wei, Hao [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Minist Educ, Xian 710069, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
C-C-BOND; RH(I)-CATALYZED DIRECT ARYLATION; C(SP(2))-C(SP(2)) SINGLE BOND; ALIPHATIC CARBOXYLIC-ACIDS; CROSS-COUPLING REACTIONS; HECK-TYPE ARYLATION; ACYL-OXYGEN BONDS; AROYL CHLORIDES; ORGANIC SYNTHESES; H FUNCTIONALIZATION;
D O I
10.1021/acs.chemrev.0c00153
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed decarbonylation via carbon-carbon bond cleavage is an essential synthetic methodology. Given the ubiquity of carbonyl compounds, the selective decarbonylative process offers a distinct synthetic strategy using carbonyl groups as "traceless handles". This reaction has been significantly developed in recent years in many respects, including catalytic system development, mechanistic understanding, substrate scope, and application in the synthesis of complex functional molecules. Therefore, this review aims to summarize the recent progress on transition-metal-catalyzed decarbonylative process, from the discovery of new transformations to the understanding of reaction mechanisms, to reveal the great achievements and potentials in this field. The contents of this review are categorized by the type of chemical bond cleavage in the decarbonylative process. The main challenges and opportunities of the decarbonylative process are also examined with the goal of expanding the application range of decarbonylation reactions.
引用
收藏
页码:365 / 411
页数:47
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