Phenyltrimethylammonium Salts as Methylation Reagents in the Nickel-Catalyzed Methylation of C−H Bonds
Methylation of C(sp2)−H bonds was achieved through the NiII‐catalyzed reaction of benzamides with phenyltrimethylammonium bromide or iodide as the source of the methyl group. The reaction has a broad scope and shows high functional‐group compatibility. The reaction is also applicable to the methylat...
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Veröffentlicht in: | Angewandte Chemie International Edition 2016-02, Vol.55 (9), p.3162-3165 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Methylation of C(sp2)−H bonds was achieved through the NiII‐catalyzed reaction of benzamides with phenyltrimethylammonium bromide or iodide as the source of the methyl group. The reaction has a broad scope and shows high functional‐group compatibility. The reaction is also applicable to the methylation of C(sp3)−H bonds in aliphatic amides.
Its all about Me! The methylation of C(sp2)−H bonds was achieved through the NiII‐catalyzed reaction of benzamides with phenyltrimethylammonium bromide or iodide as the source of the methyl group. The reaction has a broad scope and shows high functional‐group compatibility. The reaction is also applicable to the methylation of C(sp3)−H bonds in aliphatic amides. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201511197 |