Pd(II)-Catalyzed Amination of C−H Bonds Using Single-Electron or Two-electron Oxidants
Pd(II)-catalyzed intramolecular amination of arenes is developed using either a one- or two-electron oxidant. The reaction protocol tolerates a wide range of deactivating groups including acetyl, cyano, and nitro groups. This catalytic reaction allows expedient syntheses of broadly useful substitute...
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Veröffentlicht in: | Journal of the American Chemical Society 2009-08, Vol.131 (31), p.10806-10807 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Pd(II)-catalyzed intramolecular amination of arenes is developed using either a one- or two-electron oxidant. The reaction protocol tolerates a wide range of deactivating groups including acetyl, cyano, and nitro groups. This catalytic reaction allows expedient syntheses of broadly useful substituted indolines or indoles. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja904709b |