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首页> 外文期刊>Organic letters >Synthesis of unsymmetrical o-biphenols and o-binaphthols via silicon-tethered Pd-catalyzed C-H arylation
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Synthesis of unsymmetrical o-biphenols and o-binaphthols via silicon-tethered Pd-catalyzed C-H arylation

机译:硅系钯催化C-H芳基化反应合成不对称邻双酚和邻二酚

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摘要

A mild, practical, and efficient method for the synthesis of unsymmetrical o-biphenols (including o-phenol-naphthols and o-binaphthols) has been developed. Unsymmetrical bis-aryloxy silanes, which were readily prepared in a semi-one-pot fashion, underwent the Pd-catalyzed intramolecular arylation followed by a routine TBAF desilylation step to furnish valuable unsymmetrical biphenols without necessity of isolation of seven-membered intermediates. The excellent functional group tolerance allows for synthesis of a variety of functionalized o-biphenols and o-binaphthols from easily available staring materials.
机译:已经开发了一种温和,实用,有效的方法来合成不对称的邻双酚(包括邻苯酚萘酚和邻联萘酚)。不对称的双芳氧基硅烷很容易以半一锅的方式制备,经过Pd催化的分子内芳基化,然后进行常规的TBAF甲硅烷基化步骤,以提供有价值的不对称双酚,而无需分离七元中间体。出色的官能团耐受性允许从容易获得的凝视材料合成各种官能化的邻双酚和邻二酚。

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