Abstract
Transition-metal-catalyzed asymmetric C–H functionalization has become a powerful strategy to synthesize complex chiral molecules. Recently, catalytic enantioselective C–H arylation has attracted great interest from organic chemists to construct aryl-substituted chiral compounds. In this short review, we highlight recent advances in asymmetric C–H arylation from 2019 to late 2021, including enantioselective C(sp2)–H arylation to construct axial or planar chiral compounds, and enantioselective C(sp3)–H arylation to introduce central chirality via desymmetrization of the methyl group or methylene C–H activation. These processes proceed with palladium, rhodium, iridium, nickel, or copper catalysts, and utilize aryl halides, boron, or diazo derivatives as arylation reagents.
Original language | English |
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Pages (from-to) | 4734-4752 |
Number of pages | 19 |
Journal | Synthesis |
Volume | 54 |
Issue number | 21 |
Early online date | 14 Dec 2021 |
DOIs | |
Publication status | Published - Nov 2022 |
Scopus Subject Areas
- Catalysis
- Organic Chemistry
User-Defined Keywords
- arylation
- asymmetric C-H activation
- C(sp )-H arylation
- C-H bond functionalization
- chiral ligands
- transition-metal catalysis