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首页> 外文期刊>Inorganica Chimica Acta >Effective new palladium catalysts for the Suzuki coupling of various haloxylenes to prepare sterically hindered bi- and triaryls
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Effective new palladium catalysts for the Suzuki coupling of various haloxylenes to prepare sterically hindered bi- and triaryls

机译:有效的新型钯催化剂,用于各种卤代亚砜的Suzuki偶联反应,可制备位阻双芳基和三芳基

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摘要

Several new ortho-alkyl and heteroalkyl substituted aryl and aryl alkyl phosphanes and their palladium complexes have been selectively prepared, characterized and compared as potential catalysts for the Suzuki coupling reaction. The modification of the structures of the palladium complexes were made in search of the best possible catalytic activity. The novel catalysts were subsequently used to synthesize sterically hindered bi- and triaryls by coupling various bulky, unactivated bromoxylenes and chloroxylenes with a range of phenyl boronic acids under microwave irradiation. We showed that under optimized reaction conditions, very good results can be obtained with a selection of the new phosphanes and their mononuclear palladium complexes.
机译:已经选择性地制备,表征和比较了几种新的被邻烷基和杂烷基取代的芳基和芳基烷基膦及其钯配合物,作为铃木偶联反应的潜在催化剂。对钯配合物的结构进行修饰以寻求最佳的催化活性。随后,通过在微波辐射下将各种体积大的未活化溴二甲苯和氯二甲苯与一系列苯基硼酸偶联,将新型催化剂用于合成位阻双芳基和三芳基。我们表明,在优化的反应条件下,选择新的膦及其单核钯配合物可以获得非常好的结果。

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