Palladium-catalyzed direct oxidative ortho-acylation of anilides with toluene derivatives
Direct oxidative ortho-acylation reaction of anilides with toluene derivatives in the presence of palladium acetate using tert-butyl hydroperoxide as an oxidant was developed. A broad range of diaryl ketones was obtained in good to excellent yields (up to 95%). The plausible mechanism was also propo...
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Veröffentlicht in: | Tetrahedron letters 2013-03, Vol.54 (10), p.1205-1207 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Direct oxidative ortho-acylation reaction of anilides with toluene derivatives in the presence of palladium acetate using tert-butyl hydroperoxide as an oxidant was developed. A broad range of diaryl ketones was obtained in good to excellent yields (up to 95%). The plausible mechanism was also proposed. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2012.12.059 |