中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Silver-Mediated Oxidative Trifluoromethylation of Phenols: Direct Synthesis of Aryl Trifluoromethyl Ethers

文献类型:期刊论文

作者Liu JB(刘建波)1; Chen C(陈超)1; Chu LL(储玲玲)1; Chen ZH(陈增浩)1; Xu XH(徐修华)1; Qing FL(卿凤翎)1
刊名Angew. Chem.-Int. Edit.
出版日期2015
卷号54期号:40页码:11839-11842
其他题名银参与酚的氧化三氟甲基化反应: 芳基三氟甲基醚的直接合成
通讯作者卿凤翎
英文摘要Aryl trifluoromethyl ethers (ArOCF3) are prevalent in pharmaceuticals, agrochemicals, and materials. However, methods for the general and efficient synthesis of these compounds are extremely underdeveloped and limited. Herein, we describe a highly efficient and general procedure for the direct O-trifluoromethylation of unprotected phenols through a silver-mediated cross-coupling reaction using CF3SiMe3 as the CF3 source and exogenous oxidants. This novel oxidative trifluoromethylation provides access to a wide range of aryl trifluoromethyl ethers from simple phenols. The mild process was also applied to the late-stage trifluoromethylation of a medicinally relevant compound.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/anie.201506329
语种英语
WOS记录号WOS:000363394800045
源URL[http://ir.sioc.ac.cn/handle/331003/39750]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
作者单位1.中科院上海有机化学研究所, 有机氟化学重点实验室
2.东华大学
推荐引用方式
GB/T 7714
Liu JB,Chen C,Chu LL,et al. Silver-Mediated Oxidative Trifluoromethylation of Phenols: Direct Synthesis of Aryl Trifluoromethyl Ethers[J]. Angew. Chem.-Int. Edit.,2015,54(40):11839-11842.
APA 刘建波,陈超,储玲玲,陈增浩,徐修华,&卿凤翎.(2015).Silver-Mediated Oxidative Trifluoromethylation of Phenols: Direct Synthesis of Aryl Trifluoromethyl Ethers.Angew. Chem.-Int. Edit.,54(40),11839-11842.
MLA 刘建波,et al."Silver-Mediated Oxidative Trifluoromethylation of Phenols: Direct Synthesis of Aryl Trifluoromethyl Ethers".Angew. Chem.-Int. Edit. 54.40(2015):11839-11842.

入库方式: OAI收割

来源:上海有机化学研究所

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