Literature DB >> 26268604

Silver-Mediated Oxidative Trifluoromethylation of Phenols: Direct Synthesis of Aryl Trifluoromethyl Ethers.

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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  17 in total

1.  Redox-Active Reagents for Photocatalytic Generation of the OCF3 Radical and (Hetero)Aryl C-H Trifluoromethoxylation.

Authors:  Weijia Zheng; Johnny W Lee; Cristian A Morales-Rivera; Peng Liu; Ming-Yu Ngai
Journal:  Angew Chem Int Ed Engl       Date:  2018-09-20       Impact factor: 15.336

2.  Redox-Neutral TEMPO Catalysis: Direct Radical (Hetero)Aryl C-H Di- and Trifluoromethoxylation.

Authors:  Johnny W Lee; Sanghyun Lim; Daniel N Maienshein; Peng Liu; Ming-Yu Ngai
Journal:  Angew Chem Int Ed Engl       Date:  2020-09-24       Impact factor: 15.336

3.  Synthesis of Trifluoromethoxylated (Hetero)Arenes via OCF3 Migration.

Authors:  Katarzyna N Lee; Johnny W Lee; Ming-Yu Ngai
Journal:  Synlett       Date:  2015-11-16       Impact factor: 2.454

4.  Asymmetric silver-catalysed intermolecular bromotrifluoromethoxylation of alkenes with a new trifluoromethoxylation reagent.

Authors:  Shuo Guo; Fei Cong; Rui Guo; Liang Wang; Pingping Tang
Journal:  Nat Chem       Date:  2017-01-23       Impact factor: 24.427

5.  Catalytic C-H Trifluoromethoxylation of Arenes and Heteroarenes.

Authors:  Weijia Zheng; Cristian A Morales-Rivera; Johnny W Lee; Peng Liu; Ming-Yu Ngai
Journal:  Angew Chem Int Ed Engl       Date:  2018-03-13       Impact factor: 15.336

6.  Late-Stage Conversion of a Metabolically Labile Aryl Methyl Ether-Containing Natural Product to Fluoroalkyl Analogues.

Authors:  Jacob P Sorrentino; Brett R Ambler; Ryan A Altman
Journal:  J Org Chem       Date:  2020-03-27       Impact factor: 4.354

7.  Mechanistic studies on intramolecular C-H trifluoromethoxylation of (hetero)arenes via OCF3-migration.

Authors:  Katarzyna N Lee; Zhen Lei; Cristian A Morales-Rivera; Peng Liu; Ming-Yu Ngai
Journal:  Org Biomol Chem       Date:  2016-06-15       Impact factor: 3.876

8.  Trifluoromethyl Nonaflate: A Practical Trifluoromethoxylating Reagent and its Application to the Regio- and Stereoselective Synthesis of Trifluoromethoxylated Alkenes.

Authors:  Zhichao Lu; Tatsuya Kumon; Gerald B Hammond; Teruo Umemoto
Journal:  Angew Chem Int Ed Engl       Date:  2021-06-17       Impact factor: 16.823

9.  Access to a new class of synthetic building blocks via trifluoromethoxylation of pyridines and pyrimidines.

Authors:  Pengju Feng; Katarzyna N Lee; Johnny W Lee; Chengbo Zhan; Ming-Yu Ngai
Journal:  Chem Sci       Date:  2015-10-07       Impact factor: 9.825

10.  Biocatalytic trifluoromethylation of unprotected phenols.

Authors:  Robert C Simon; Eduardo Busto; Nina Richter; Verena Resch; Kendall N Houk; Wolfgang Kroutil
Journal:  Nat Commun       Date:  2016-11-11       Impact factor: 14.919

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