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首页> 外文期刊>Journal of Organometallic Chemistry >Efficient Suzuki coupling tricyclohexylphosphine adducts of aryl chlorides catalyzed by of cyclopalladated ferrocenylimines
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Efficient Suzuki coupling tricyclohexylphosphine adducts of aryl chlorides catalyzed by of cyclopalladated ferrocenylimines

机译:高效的铃木偶联三环己基膦的三环己基膦加合物,由环钯制的二茂铁基亚胺催化

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摘要

The air and moisture stable tricyclohexylphosphine (PCY3) adducts of dimeric cyclopalladated ferrocenylimines 5 and 6 have been easily synthesized and successfully used in palladium-catalyzed Suzuki cross-coupling of aryl chlorides. Using 0.1 mol% of 6 in the presence of 2 equivalent Of CS2CO3 as base in dioxane at 100 degrees C provided coupled products in excellent yields in the reaction of non-activated and deactivated aryl chlorides with phenylboronic acid. For activated chlorides such as 4-chloronitrobenzene and 4-chloroacetophenone, the catalyst loadings could be lowered to 0.01 mol% without loss of activity. (c) 2005 Elsevier B.V. All rights reserved.
机译:易于合成的具有空气和湿气稳定性的二聚环palladated二茂铁基亚胺5和6的三环己基膦(PCY3)加合物已成功地用于钯催化的芳基氯的Suzuki交叉偶联。在100℃下在二恶烷中在2当量的CS 2 CO 3作为碱存在下使用0.1mol%的6,在未活化和失活的芳基氯与苯基硼酸的反应中以优异的产率提供了偶联产物。对于活化的氯化物,例如4-氯硝基苯和4-氯苯乙酮,催化剂的负载量可以降低到0.01mol%而不会损失活性。 (c)2005 Elsevier B.V.保留所有权利。

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