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可见光铜光氧化还原催化的酚和末端炔烃的有氧偶联:通过 C≡C 三键断裂的官能化酮的区域选择性合成。

Visible Light Copper Photoredox-Catalyzed Aerobic Oxidative Coupling of Phenols and Terminal Alkynes: Regioselective Synthesis of Functionalized Ketones via C≡C Triple Bond Cleavage.

机构信息

Department of Chemistry, National Tsing Hua University , Hsinchu, Taiwan, R. O. C.

出版信息

J Am Chem Soc. 2017 Mar 1;139(8):2896-2899. doi: 10.1021/jacs.6b13113. Epub 2017 Feb 15.

Abstract

Direct oxidative coupling of phenols and terminal alkynes was achieved at room temperature by a visible-light-mediated copper-catalyzed photoredox process. This method allows regioselective synthesis of hydroxyl-functionalized aryl and alkyl ketones from simple phenols and phenylacetylene via C≡C triple bond cleavage. 47 examples were presented. From a synthetic perspective, this protocol offers an efficient synthetic route for the preparation of pharmaceutical drugs, such as pitofenone and fenofibrate.

摘要

通过可见光介导的铜催化光氧化还原过程,在室温下实现了酚和末端炔烃的直接氧化偶联。该方法允许通过 C≡C 三键断裂,从简单的苯酚和苯乙炔中区域选择性合成羟基官能化的芳基和烷基酮。展示了 47 个实例。从合成的角度来看,该方案为制备药物如匹伐他汀和非诺贝特提供了一种有效的合成途径。

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