1
ChemInform 2010, 41, issue 13 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Polyphenyl derivatives Q 0700 DOI: 10.1002/chin.201013085 Efficient Suzuki—Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle. — A complex formed in situ from tri-tert-butylphosphinium tetrafluoroborate and the oxime palladacycle OPC is found to be an efficient catalyst for the Suzuki coupling of a variety of aryl chlorides in the presence of Bu4NOH as the co-catalyst. — (ALONSO*, D. A.; CIVICOS, J. F.; NAJERA, C.; Synlett 2009, 18, 3011-3015; Dep. Quim. Org., Fac. Cienc., Univ. Alicante, E-03080 Alicante, Spain; Eng.) — Mais 13- 085

ChemInform Abstract: Efficient Suzuki—Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle

Embed Size (px)

Citation preview

www.cheminform.wiley-vch.de

Polyphenyl derivativesQ 0700 DOI: 10.1002/chin.201013085

Efficient Suzuki—Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle. — A complex formed in situ from tri-tert-butylphosphinium tetrafluoroborate and the oxime palladacycle OPC is found to be an efficient catalyst for the Suzuki coupling of a variety of aryl chlorides in the presence of Bu4NOH as the co-catalyst. — (ALONSO*, D. A.; CIVICOS, J. F.; NAJERA, C.; Synlett 2009, 18, 3011-3015; Dep. Quim. Org., Fac. Cienc., Univ. Alicante, E-03080 Alicante, Spain; Eng.) — Mais

13- 085

ChemInform 2010, 41, issue 13 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim