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首页> 外文期刊>European journal of inorganic chemistry >[(1,3-Bis{2,6-bis(diphenylmethyl)-4-methylphenyl}imidazole- 2-ylidene)PdCl_2(NEt3)]: 'Throwing Away' a Different Ancillary Ligand to Enhance the Catalytic Activity at Room Temperature
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[(1,3-Bis{2,6-bis(diphenylmethyl)-4-methylphenyl}imidazole- 2-ylidene)PdCl_2(NEt3)]: 'Throwing Away' a Different Ancillary Ligand to Enhance the Catalytic Activity at Room Temperature

机译:[(1,3-双{2,6-双(二苯基甲基)-4-甲基苯基}咪唑-2-亚基)PdCl_2(NEt3)]:“扔掉”另一种辅助配体以增强室温下的催化活性

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摘要

A considerable effort in ligand design for catalysis in recent years has led to remarkable achievements in cross-coupling reactions. In this work, we show that a careful selection of the ancillary ligands that complete the catalyst/precatalyst can provide an extra level of performance. Low loadings of [(IPr*)PdCl_2(TEA)] {IPr* = 1,3-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]imidazole-2-ylidene, TEA = triethylamine} catalyze the Buchwald-Hartwig amination reactions of aryl chlorides at room temperature in excellent yields, without the need for an inert atmosphere to set up or perform the reactions.
机译:近年来,在用于催化的配体设计上的大量努力已在交叉偶联反应中取得了令人瞩目的成就。在这项工作中,我们表明,精心选择可以完成催化剂/预催化剂的辅助配体可以提供更高的性能。低负荷的[((IPr *)PdCl_2(TEA)] {IPr * = 1,3-双[2,6-双(二苯甲基)-4-甲基苯基]咪唑-2-亚烷基,TEA =三乙胺}催化布赫瓦尔德-芳基氯化物在室温下以优异的收率进行Hartwig胺化反应,无需惰性气氛来建立或进行反应。

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