Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp(3))-H and C(sp(2))-H activation reactions of 3-alkylbenzofurans
A protocol involving facile sequential C(sp(3))-H and C(sp(2))-H activation reactions of 3-alkylbenzofurans catalyzed by Pd(OAc)2 in the presence of pivalic acid, silver salt, and tricyclohexylphosphine 'on water' was developed. Aryl iodides were used as substrates in a tandem bisarylation...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2015-01, Vol.51 (77), p.14543-14546 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A protocol involving facile sequential C(sp(3))-H and C(sp(2))-H activation reactions of 3-alkylbenzofurans catalyzed by Pd(OAc)2 in the presence of pivalic acid, silver salt, and tricyclohexylphosphine 'on water' was developed. Aryl iodides were used as substrates in a tandem bisarylation reaction to generate 3-arylalkyl-2-arylbenzofurans in moderate to high yields at room temperature. The reaction revealed in this study is a rare example of consecutive C(sp(3))-H and C(sp(2))-H bond activation under mild reaction conditions. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c5cc04052c |