Suzuki–Miyaura coupling reaction of aryl chlorides using di (2, 6-dimethylmorpholino) phenylphosphine as ligand

…, HK Kim, H Yim, MR Kim, JK Lee, JJ Kim, YJ Yoon

Index: Cho, Su-Dong; Kim, Ho-Kyun; Yim, Heung-seop; Kim, Mi-Ra; Lee, Jin-Kook; Kim, Jeum-Jong; Yoon, Yong-Jin Tetrahedron, 2007 , vol. 63, # 6 p. 1345 - 1352

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Citation Number: 45

Abstract

Pd-catalyzed cross-coupling reactions have become an extremely versatile tool in organic synthesis for connecting two fragments via formation of a carbon–carbon bond or carbon–heteroatom bond. 1, 2, 3 and 4 The Pd-catalyzed Suzuki–Miyaura coupling reaction is one of the most attractive method for preparing biaryl compounds thanks to the advantages of wide functional group tolerance and use of stable and nontoxic organoborane reagents. 5, 6, 7, 8, 9, 10, 11, 12 and 13 ...