Transition-metal-catalyzed enantioselective C-H silylation

被引:45
|
作者
Ge, Yicong [1 ,2 ,3 ]
Huang, Xingfen [1 ,2 ]
Ke, Jie [1 ,2 ]
He, Chuan [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Guangdong, Peoples R China
[3] Leshan Normal Univ, Sichuan Prov Key Lab Nat Prod & Small Mol Synth, Sch New Energy Mat & Chem, Leshan 614000, Sichuan, Peoples R China
来源
CHEM CATALYSIS | 2022年 / 2卷 / 11期
基金
中国国家自然科学基金;
关键词
SILICON-STEREOGENIC SILANES; ASYMMETRIC-SYNTHESIS; KINETIC RESOLUTION; DEHYDROGENATIVE SILYLATION; CHIRALITY TRANSFER; STEREOSELECTIVE SILYLATION; ORGANIC DERIVATIVES; TERTIARY SILANES; CARBON; DESYMMETRIZATION;
D O I
10.1016/j.checat.2022.07.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Organosilanes are important and valuable compounds that have found widespread applications in the fields of organic chemistry, agrochemistry, medicinal chemistry, and materials science. In modern synthetic chemistry, molecules featuring carbon-silicon bonds have attracted considerable interest given that these motifs can be efficiently converted to a wide range of functionalities. Among various approaches, transition-metal-catalyzed C-H silylation has emerged as a powerful tool for the synthesis of silicon-containing functional molecules, which has profoundly accelerated the iteration of organosilicon science. Despite the rapid development of C-H silylation, the enantioselective version of this elegant methodology was not known until 2013. In this review, we aim to summarize recent advances in the area of enantioselective C-H silylation mediated by chiral transition-metal catalysts, organized by the different forms of chirality of the enantioenriched organosilanes. We highlight the great potential of this methodology and intend to inspire further research and applications in this emerging area.
引用
收藏
页码:2898 / 2928
页数:31
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