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1, 1 '-bis(oxazolinyl)ferrocene-based palladium catalysts: Synthesis, X-ray structures and applications in Suzuki and Heck coupling reactions

机译:1,1'-双(恶唑啉基)二茂铁基钯催化剂:合成,X射线结构及其在Suzuki和Heck偶联反应中的应用

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摘要

1,1'-Bis(oxazolinyl)ferrocene-based palladium dichloride complexes 2a and 2b were synthesized. X-ray single-crystal diffraction analyses showed that they are of the N,N'-chelating type, and that the coordination mode of 2a, which has an isopropyl group, is of the cis type, whereas that of 2b, which has a tert-butyl group, is the trans one. These two complexes were employed as catalysts for Suzuki and Heck reactions, and showed high catalytic activities in coupling reactions with various aryl halides and counterparts (phenylboronic acid or n-butyl acrylate). Particularly, the catalyst 2a afforded the coupled product of aryl bromide with phenylboronic acid at room temperature. (c) 2005 Elsevier B.V. All rights reserved.
机译:合成了基于1,1'-双(恶唑啉基)二茂铁的二氯化钯配合物2a和2b。 X射线单晶衍射分析表明,它们是N,N'螯合型,具有异丙基的2a的配位模式是顺式,而具有b的2b的配位模式是顺式。叔丁基是反式的。这两种络合物用作Suzuki和Heck反应的催化剂,在与各种芳基卤化物和对应物(苯基硼酸或丙烯酸正丁酯)的偶联反应中显示出高催化活性。特别是,催化剂2a在室温下得到芳基溴化物与苯基硼酸的偶合产物。 (c)2005 Elsevier B.V.保留所有权利。

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