Palladium-catalyzed Suzuki–Miyaura reaction using aminophosphine as ligand
J Cheng, F Wang, JH Xu, Y Pan, Z Zhang
Index: Cheng, Jiang; Wang, Feng; Xu, Jian-Hua; Pan, Yi; Zhang, Zhaoguo Tetrahedron Letters, 2003 , vol. 44, # 37 p. 7095 - 7098
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Citation Number: 45
Abstract
Palladium-catalyzed cross-coupling reactions between aryl (alkenyl) halides or triflates and organometallic reagents (Mg, Sn, B, Zn, Li, Zr, etc.) have been developed as a versatile and efficient method for a variety of synthetic transformations. 1., , , , , and Among these reactions, palladium-catalyzed cross-coupling reaction between aryl halides and aryl boronic acids, known as Suzuki–Miyaura reaction, is highly valuable for the synthesis of symmetrical and unsymmetrical biaryls. 2., ...
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