Issue 77, 2015

Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp3)–H and C(sp2)–H activation reactions of 3-alkylbenzofurans

Abstract

A protocol involving facile sequential C(sp3)–H and C(sp2)–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(sp3)–H and C(sp2)–H bond activation under mild reaction conditions.

Graphical abstract: Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp3)–H and C(sp2)–H activation reactions of 3-alkylbenzofurans

Supplementary files

Article information

Article type
Communication
Submitted
19 May 2015
Accepted
07 Aug 2015
First published
19 Aug 2015

Chem. Commun., 2015,51, 14543-14546

Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp3)–H and C(sp2)–H activation reactions of 3-alkylbenzofurans

B. S. Cho and Y. K. Chung, Chem. Commun., 2015, 51, 14543 DOI: 10.1039/C5CC04052C

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