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Synthesis 2010(18): 3163-3173
DOI: 10.1055/s-0030-1258181
DOI: 10.1055/s-0030-1258181
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New YorkFacile Access to Biaryls and 2-Acetyl-5-arylbenzofurans via Suzuki Coupling in Water under Thermal and Microwave Conditions
Further Information
Received
12 March 2010
Publication Date:
16 July 2010 (online)
Publication History
Publication Date:
16 July 2010 (online)
Abstract
The phosphine-free Suzuki-Miyaura carbon-carbon cross-coupling reactions of activated and deactivated aryl halides and 2-acetyl-5-bromobenzofuran with various aryl- or heteroarylboronic acids were investigated. A benzothiazole-based palladium(II) complex was used as a precatalyst for the reactions under both thermal and microwave conditions in air using water as a solvent.
Key words
palladium - catalysis - microwave irradiation - Suzuki reactions - benzofuran
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