NDLI: Suzuki-Miyaura Coupling of Aryl Chlorides with Supported Palladium Catalyst

Content Provider	Scilit
Author	Schweizer, S.
Editor	Becht, J. -M. Drian, C. Le
Copyright Year	2010
Description	Polymer-supported palladium catalyst 1 was prepared by the reaction of Merrifield resin with lithium tert-butylphenylphosphide, followed by treatment with tetrakis(triphenylphosphine)palladium (eq. 1). The catalyst 1 promoted the Suzuki-Miyaura cross-coupling reactions of aryl chlorides 2 with arylboronic acids 3 to give the corresponding biaryls 4 in up to 98% yield (17 examples, eq. 2).
Related Links	http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0029-1219279.pdf
Ending Page	0373
Page Count	1
Starting Page	0373
ISSN	18611958
e-ISSN	1861194X
DOI	10.1055/s-0029-1219279
Journal	Synfacts
Issue Number	03
Volume Number	2010
Language	English
Publisher	Georg Thieme Verlag KG
Publisher Date	2010-02-18
Access Restriction	Open
Subject Keyword	Journal: Synfacts Organic Chemistry Aryl Chlorides Em Class
Content Type	Text
Resource Type	Synopsis

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Suzuki-Miyaura Coupling of Aryl Chlorides with Supported Palladium Catalyst