首页> 外文期刊>European journal of inorganic chemistry >Palladium-catalyzed Suzuki-Miyaura cross-coupling of various aryl halides using ortho-alkyl-substituted arylphosphanes and (ortho-alkylphenyl)-alkylphosphanes under microwave heating
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Palladium-catalyzed Suzuki-Miyaura cross-coupling of various aryl halides using ortho-alkyl-substituted arylphosphanes and (ortho-alkylphenyl)-alkylphosphanes under microwave heating

机译:在微波加热下,使用邻烷基取代的芳基膦和(邻烷基苯基)-烷基膦,钯催化的各种芳基卤化物的Suzuki-Miyaura交叉偶联

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摘要

Mono- and dinuclear palladium(II) chloride complexes of various ortho-alkyl-substituted aryl- and alkylphosphanes were prepared. Subsequently, these were characterized by H-1 NMR and P-31(H-1) NMR spectroscopy, X-ray crystallographic studies and mass spectroscopy. The palladium complexes were screened as potential catalysts for the microwave-assisted Suzuki-Miyaura coupling reaction of several aryl halides under aerobic conditions. A preliminary study showed that excellent results can be obtained even for electron-rich bromides and unactivated aryl chlorides with an optimized solvent, base and catalyst loading using specific phosphane ligands. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).
机译:制备了各种邻烷基取代的芳基和烷基膦的单核和双核氯化钯(II)配合物。随后,通过H-1 NMR和P-31(H-1)NMR光谱,X射线晶体学研究和质谱对它们进行表征。筛选了钯配合物作为好氧条件下几种芳基卤化物的微波辅助Suzuki-Miyaura偶联反应的潜在催化剂。初步研究表明,即使是富电子的溴化物和未活化的芳基氯化物,使用特定的膦配体,也可以优化溶剂,碱和催化剂的负载量,也可以获得出色的结果。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2008)。

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