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首页> 外文期刊>Bulletin of the Korean Chemical Society >Facile Access to a Variety of 2,5-Biaryl-1,2,4-triazol-3-ones via Regioselective N-Arylation of Triazolones
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Facile Access to a Variety of 2,5-Biaryl-1,2,4-triazol-3-ones via Regioselective N-Arylation of Triazolones

机译:通过三唑酮的区域选择性N-芳基化轻松获得各种2,5-联芳基1,2,4-三唑-3-酮

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摘要

A selective synthetic method of the 2,5-biaryltriazolones has been developed via copper-catalyzed N-arylation reaction. Aryltriazolones, which were readily prepared from commercially available compounds, were N-arylated to 2,5-biaryltriazolones with high regioselectivity. This approach allows for access to a variety of 2,5-biaryl-1,2,4-trizol-3-ones in a simple and practical manner.
机译:通过铜催化的N-芳基化反应,已经开发出一种选择性合成2,5-联芳基三唑酮的方法。由市售化合物容易制备的芳基三唑酮以高区域选择性被N-芳基化为2,5-联芳基三唑酮。该方法允许以简单和实用的方式获得各种2,5-二芳基-1,2,4-三唑-3-酮。

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