An active ferrocenyl triarylphosphine for palladium-catalyzed Suzuki–Miyaura cross-coupling of aryl halides

Literature Information

Publication Date 2004-09-21
DOI 10.1039/B407661C
Impact Factor 6.222
Authors

Fuk Yee Kwong, Kin Shing Chan, Chi Hung Yeung, Albert S. C. Chan


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Abstract

Pd-catalyzed Suzuki–Miyaura reaction of aryl chlorides was accomplished through the use of an active ferrocene-based triarylphosphine ligand. This air- and moisture-stable ligand was found to be effective for the cross-coupling of aryl halides at room temperature to 115 °C.

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