Copper-mediated C-H bond arylation of arenes with arylboronic acids
被引:140
作者:
Ban, Ikuya
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Nagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, JapanNagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
Ban, Ikuya
[1
]
Sudo, Tomoko
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Nagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, JapanNagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
Sudo, Tomoko
[1
]
Taniguchi, Tadashi
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机构:Nagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
Taniguchi, Tadashi
Itami, Kenichiro
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Nagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
Japan Sci & Technol Agcy, PRESTO, Kanagawa, JapanNagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
Itami, Kenichiro
[1
,2
]
机构:
[1] Nagoya Univ, Grad Sch Sci, Dept Chem, Nagoya, Aichi 4648602, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kanagawa, Japan
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 biaryis 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 pi-systems.