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
Hauptverfasser: Ban, Ikuya, Sudo, Tomoko, Taniguchi, Tadashi, Itami, Kenichiro
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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.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol8013717