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室温下通过二芳基碘鎓盐与磷亲核试剂的直接偶联实现铜催化的 P-芳基化反应。

Copper-catalyzed P-arylation via direct coupling of diaryliodonium salts with phosphorus nucleophiles at room temperature.

机构信息

Department of Chemistry, College of Chemistry and Chemical Engineering, and the Key Laboratory for Chemical Biology of Fujian Province, Xiamen University, Xiamen, Fujian 361005, China.

出版信息

J Org Chem. 2013 Aug 16;78(16):8176-83. doi: 10.1021/jo4012199. Epub 2013 Jul 30.

Abstract

A new method for copper-catalyzed P-C bond formation through reaction of phosphorus nucleophiles with diaryliodonium salts at room temperature is described. Most target products are obtained with this method in high yields within a short reaction time of 10 min. It can be easily adapted to large-scale preparations. When unsymmetrical iodonium salts are employed, nucleophilic substitution occurs preferentially on the sterically hindered aromatic ring or the more electron-deficient ring.

摘要

描述了一种新的室温条件下通过磷亲核试剂与二芳基碘𬭩盐反应形成 P-C 键的方法。该方法可在 10 分钟的短反应时间内以高产率获得大多数目标产物。它可以很容易地适应于大规模制备。当使用不对称碘𬭩盐时,亲核取代优先发生在空间位阻较大的芳环或缺电子环上。

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