Copper-Mediated C−H Bond Arylation of Arenes with Arylboronic Acids
A new copper-mediated cross-coupling of arenes and arylboronic acids is described. Under the influence of Cu(OCOCF3)2, the C−H bond arylation of electron-rich arenes with arylboronic acids takes place to afford a range of biaryls in good yields. The reaction is selective for cross-coupling; no homoc...
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Veröffentlicht in: | Organic letters 2008-08, Vol.10 (16), p.3607-3609 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new copper-mediated cross-coupling of arenes and arylboronic acids is described. Under the influence of Cu(OCOCF3)2, the C−H bond arylation of electron-rich arenes with arylboronic acids takes place to afford a range of biaryls in good yields. The reaction is selective for cross-coupling; no homocoupling product arising from arenes or arylboronic acids is detected. Multiple C−H bond arylation is possible with indoles and pyrroles furnishing interesting extended π-systems. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol8013717 |