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- W4324129128 abstract "Despite the notable advances achieved in the Murai-type hydroarylations, highly enantioselective catalytic addition of native (hetero)arenes to internal alkenes remains a prominent challenge. Herein, we report a directing group repositioning strategy, which enables the iridium-catalyzed enantioselective addition of heteroarenes including furan, benzofuran, and thiophene to internal enamides. The C–H bond at the C2 position of the heteroarene is site-selectively cleaved and added regioselectively to the β-position of an enamide, affording a valuable β-heteroaryl amide with high enantioselectivity. Mechanistic studies indicate that the rate and the enantioselectivity are determined by separate elementary steps." @default.
- W4324129128 created "2023-03-15" @default.
- W4324129128 creator A5008663016 @default.
- W4324129128 creator A5083004837 @default.
- W4324129128 date "2023-03-14" @default.
- W4324129128 modified "2023-10-12" @default.
- W4324129128 title "Directing Group Repositioning Strategy Enabled Site- and Enantioselective Addition of Heteroaromatic C–H Bonds to Acyclic Internal Alkenes" @default.
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- W4324129128 doi "https://doi.org/10.1021/jacs.3c00095" @default.
- W4324129128 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36917558" @default.
- W4324129128 hasPublicationYear "2023" @default.
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