Palladium‐catalyzed C H acetoxylation of arenes using a pyrazolonaphthyridine ligand
Herein, Pd‐catalyzed CH acetoxylation reactions of arenes are developed using a pyrazolonaphthyridine ligand. In the presence of iodomesitylene diacetate as the oxidant, the electron‐deficient ligand facilitates the CH activation of the electron‐rich positions while preventing the formation of Pd...
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Veröffentlicht in: | Bulletin of the Korean Chemical Society 2022-10, Vol.43 (10), p.1173-1176 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Herein, Pd‐catalyzed CH acetoxylation reactions of arenes are developed using a pyrazolonaphthyridine ligand. In the presence of iodomesitylene diacetate as the oxidant, the electron‐deficient ligand facilitates the CH activation of the electron‐rich positions while preventing the formation of Pd black via bidentate binding. Although both acetic acid and hexafluoroisopropanol are employed for directing group‐assisted acetoxylation reactions, the latter proved to be more efficient for the nondirected reaction of arenes with the nitrogen ligand. |
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ISSN: | 1229-5949 1229-5949 |
DOI: | 10.1002/bkcs.12599 |