Volume 120, Issue 42 pp. 8179-8183
Zuschrift

A General Palladium-Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates

Chau Ming So

Chau Ming So

Open Laboratory of Chirotechnology, The Institute of Molecular Technology for Drug Discovery and Synthesis, Department of Applied Biology and Chemical Technology, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (Hong Kong), Fax: (+852) 2364-9932

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Chak Po Lau Prof. Dr.

Chak Po Lau Prof. Dr.

Open Laboratory of Chirotechnology, The Institute of Molecular Technology for Drug Discovery and Synthesis, Department of Applied Biology and Chemical Technology, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (Hong Kong), Fax: (+852) 2364-9932

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Fuk Yee Kwong Prof. Dr.

Fuk Yee Kwong Prof. Dr.

Open Laboratory of Chirotechnology, The Institute of Molecular Technology for Drug Discovery and Synthesis, Department of Applied Biology and Chemical Technology, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (Hong Kong), Fax: (+852) 2364-9932

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First published: 29 September 2008
Citations: 60

We thank the Research Grants Council of Hong Kong (Project No. CERG: PolyU5008/06P) and University Grants Committee Areas of Excellence Scheme (Project No. AoE/P-10/01) for financial support.

Graphical Abstract

Katalysier das! Die hier vorgestellte erste palladiumkatalysierte Suzuki-Miyaura-Kupplung nicht aktivierter Arylmesylate gelingt nicht nur mit Arylboronsäuren, sondern auch mit anderen Organobor-Nucleophilen (Z=B(OH)2, BF3K, BPin), und die Reaktionsbedingungen sind mit einer Vielzahl gängiger funktioneller Gruppen (R1=Alkyl, OMe, CHO, CO, CN, CO2R′, Heteroaryl) kompatibel.

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