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首页> 外文期刊>Synthetic Communications >Ligand-free copper-catalyzed O-arylation of arenesulfonamides with phenols: An unusual approach to biaryl ether synthesis
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Ligand-free copper-catalyzed O-arylation of arenesulfonamides with phenols: An unusual approach to biaryl ether synthesis

机译:与酚醛氟磺酰胺的无配体铜催化的O-芳基化合物:苯甲酸醚合成的不寻常方法

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摘要

An unprecedented ligand-free copper-catalyzed O-arylation of arenesulfonamides with phenols has been developed. Thus, a range of unsysmmetric biaryl ethers were synthesized in excellent yields. The reaction occurs efficiently with excellent regioselectivity through the cleavage of C-ary-S bond and with a good tolerance of functional groups on the phenyl ring of phenols. The reaction is appreciated for its readily accessible substrates, mild conditions, and simple operation under air.
机译:已经开发出具有苯酚的前所未有的无配体铜催化的O-芳苯胺。 因此,以优异的产率合成了一系列不甜味的芳烃醚。 反应有效地发生,通过C-芳基-S键的切割有效地具有优异的区域选择性,并且在酚的苯基环上具有良好的官能团的耐受性。 其易于可接近的基材,温和条件和空气下的简单操作,应当理解该反应。

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