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ChemInform 2010, 41, issue 16 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Phenol ethers Q 0270 DOI: 10.1002/chin.201016058 Efficient Palladium-Catalyzed Coupling Reactions of Aryl Bromides and Chlo- rides with Phenols. — Various functional groups are tolerated in the title reaction. In general, aryl halides (I) with electron-withdrawing groups give higher yields compared to aryl residues with electron-donating substituents. — (HU, T.; SCHULZ, T.; TORBORG, C.; CHEN, X.; WANG, J.; BELLER, M.; HUANG*, J.; Chem. Commun. (Cambridge) 2009, 47, 7330-7332; State Key Lab. Mater.-Oriented Chem. Eng., Coll. Mater. Sci. Eng., Nanjing Univ. Technol., Nanjing 210009, Peop. Rep. China; Eng.) — M. Paetzel 16- 058

ChemInform Abstract: Efficient Palladium-Catalyzed Coupling Reactions of Aryl Bromides and Chlorides with Phenols

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Phenol ethersQ 0270 DOI: 10.1002/chin.201016058

Efficient Palladium-Catalyzed Coupling Reactions of Aryl Bromides and Chlo-rides with Phenols. — Various functional groups are tolerated in the title reaction. In general, aryl halides (I) with electron-withdrawing groups give higher yields compared to aryl residues with electron-donating substituents. — (HU, T.; SCHULZ, T.; TORBORG, C.; CHEN, X.; WANG, J.; BELLER, M.; HUANG*, J.; Chem. Commun. (Cambridge) 2009, 47, 7330-7332; State Key Lab. Mater.-Oriented Chem. Eng., Coll. Mater. Sci. Eng., Nanjing Univ. Technol., Nanjing 210009, Peop. Rep. China; Eng.) — M. Paetzel

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ChemInform 2010, 41, issue 16 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim