Functionalization of arylacetic acids via directing-group-assisted remote meta -C-H activation
Herein, we report the first microwave-assisted remote-C-H functionalization aided by a simple nitrile directing template. Notably, the present protocol showed a broad substrate scope enabling -C-H arylation, acetoxylation, and cyanation. Significantly, the microwave-accelerated -C-H functionalizatio...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2023-06, Vol.59 (46), p.7084-7087 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Herein, we report the first microwave-assisted remote-C-H functionalization aided by a simple nitrile directing template. Notably, the present protocol showed a broad substrate scope
enabling
-C-H arylation, acetoxylation, and cyanation. Significantly, the microwave-accelerated
-C-H functionalization was effective with short reaction times without compromising yields and site selectivity. In addition, ibuprofen drug diversification was accomplished by carrying out arylation, acetoxylation, and cyanation. Importantly,
-dual-hetero functionalization has been presented. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d3cc01050c |