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首页> 外文期刊>The Journal of Organic Chemistry >Phosphine-Free, Heterogeneous Palladium-Catalyzed Atom-Efficient Carbonylative Cross-Coupling of Triarylbismuths with Aryl Iodides: Synthesis of Biaryl Ketones
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Phosphine-Free, Heterogeneous Palladium-Catalyzed Atom-Efficient Carbonylative Cross-Coupling of Triarylbismuths with Aryl Iodides: Synthesis of Biaryl Ketones

机译:三芳基铋与芳基碘化物的无磷,异质钯催化原子高效羰基交叉偶联:联芳基酮的合成

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摘要

A novel and highly efficient heterogeneous palladium-catalyzed carbonylative cross-coupling of aryl iodides with triarylbismuths has been developed that proceeds smoothly at atmospheric CO pressure and provides a general and powerful tool for the preparation of various valuable biaryl ketones with high atom economy, good to excellent yield, and recyclability of the catalyst. The reaction is the first example of Pd-catalyzed carbonylative cross-coupling for the construction of biaryl ketones using triarylbismuths as substrates.
机译:已开发出一种新颖且高效的钯钯催化的芳基碘化物与三芳基铋的羰基交叉偶联反应,该反应在大气CO压力下可顺利进行,并为制备各种有价值的,具有高原子经济性的有价值的联芳基酮提供了通用而强大的工具。优异的产率和催化剂的可回收性。该反应是使用三芳基铋作为底物构建联芳基酮的钯催化羰基交叉偶联的第一个例子。

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