| Literature DB >> 26268604 |
Jian-Bo Liu1, Chao Chen1, Lingling Chu1, Zeng-Hao Chen1, Xiu-Hua Xu1, Feng-Ling Qing2,3.
Abstract
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 CF3 SiMe3 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.Entities:
Keywords: fluorine; oxidative coupling; phenols; silver; trifluoromethylation
Year: 2015 PMID: 26268604 DOI: 10.1002/anie.201506329
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336