Title | Transition-metal-catalyzed enantioselective C−H silylation |
Author | |
Corresponding Author | He,Chuan |
Publication Years | 2022-11-17
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DOI | |
Source Title | |
ISSN | 2667-1107
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EISSN | 2667-1093
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Volume | 2Issue:11Pages:2898-2928 |
Abstract | 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. |
Keywords | |
URL | [Source Record] |
Language | English
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SUSTech Authorship | First
; Corresponding
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Funding Project | Guangdong Provincial Key Laboratory Of Catalysis[2020B121201002];National Natural Science Foundation of China[21901104];National Natural Science Foundation of China[22101113];National Natural Science Foundation of China[22101120];National Natural Science Foundation of China[22122102];
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Scopus EID | 2-s2.0-85141990313
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Data Source | Scopus
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Citation statistics |
Cited Times [WOS]:5
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Document Type | Journal Article |
Identifier | http://kc.sustech.edu.cn/handle/2SGJ60CL/416316 |
Department | Department of Chemistry 深圳格拉布斯研究院 |
Affiliation | 1.Shenzhen Grubbs Institute and Department of Chemistry,Guangdong Provincial Key Laboratory of Catalysis,Southern University of Science and Technology,Shenzhen,Guangdong,518055,China 2.Sichuan Province Key Laboratory of Natural Products and Small Molecule Synthesis,School of New Energy Materials and Chemistry,Leshan Normal University,Leshan,Sichuan,614000,China |
First Author Affilication | Department of Chemistry; Shenzhen Grubbs Institute |
Corresponding Author Affilication | Department of Chemistry; Shenzhen Grubbs Institute |
First Author's First Affilication | Department of Chemistry; Shenzhen Grubbs Institute |
Recommended Citation GB/T 7714 |
Ge,Yicong,Huang,Xingfen,Ke,Jie,et al. Transition-metal-catalyzed enantioselective C−H silylation[J]. Chem Catalysis,2022,2(11):2898-2928.
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APA |
Ge,Yicong,Huang,Xingfen,Ke,Jie,&He,Chuan.(2022).Transition-metal-catalyzed enantioselective C−H silylation.Chem Catalysis,2(11),2898-2928.
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MLA |
Ge,Yicong,et al."Transition-metal-catalyzed enantioselective C−H silylation".Chem Catalysis 2.11(2022):2898-2928.
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