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Synthesis 2011(8): 1295-1301
DOI: 10.1055/s-0030-1258472
DOI: 10.1055/s-0030-1258472
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New YorkRecyclable Catalysts for Suzuki-Miyaura Cross-Coupling Reactions at Ambient Temperature Based on a Simple Merrifield Resin Supported Phenanthroline-Palladium(II) Complex
Further Information
Received
7 January 2011
Publication Date:
10 March 2011 (online)
Publication History
Publication Date:
10 March 2011 (online)
Abstract
A novel Merrifield resin immobilized phenanthroline-palladium(II) complex has been developed and was found to be an efficient catalyst for Suzuki-Miyaura cross-coupling reaction between arylboronic acids and a range of aryl halides under mild reaction conditions. The catalyst exhibited both high catalytic activity and stability for Suzuki-Miyaura reaction. Furthermore, the catalyst could be recycled at least 10 times without a significant loss of catalytic activity.
Key words
immobilized catalyst - phenanthroline-palladium(II) complex - Suzuki-Miyaura reaction - recyclability
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