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首页> 外文期刊>Applied Organometallic Chemistry >pH-Dependent conjugate addition of arylboronic acids to α,β-unsaturated enones catalyzed by a reusable palladium(II)/cationic 2,2-bipyridyl system in water under air
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pH-Dependent conjugate addition of arylboronic acids to α,β-unsaturated enones catalyzed by a reusable palladium(II)/cationic 2,2-bipyridyl system in water under air

机译:空气中水中可重复使用的钯(II)/阳离子2,2-联吡啶系统催化将pH依赖的芳基硼酸共轭加成到α,β-不饱和烯酮上

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摘要

A reusable Pd(NH3)2Cl2/cationic 2,2-bipyridyl system for the catalysis of the conjugate addition of arylboronic acids to α,β-unsaturated enones in water under air was developed. Addition of arylboronic acids to both cyclic and acyclic enones progressed smoothly, providing the products in good to high yields, the best result being obtained when HBF4 was used to adjust the pH value to 1.0. After the reaction, the residual aqueous solution could be reused several times, making the reaction greener and reducing wastage of precious metals.
机译:开发了可重复使用的Pd(NH3)2Cl2 /阳离子2,2-联吡啶系统,用于在空气中催化芳基硼酸共轭加成到水中的α,β-不饱和烯酮上。芳基硼酸在环状和无环烯酮中的添加均进展顺利,提供了高至高收率的产物,当使用HBF4将pH值调节至1.0时可获得最佳结果。反应后,残留的水溶液可以重复使用几次,使反应更环保,并减少了贵金属的浪费。

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