Literature DB >> 30906076

Recent Development of Catalytic Trifluoromethoxylation Reactions.

Katarzyna N Lee1, Johnny W Lee1, Ming-Yu Ngai1,2.   

Abstract

Trifluoromethoxy (OCF3) group exhibits unique properties, which render it a highly desirable structural motif in life and materials sciences. The numbers of newly synthesized trifluoromethyl ethers are booming as new synthetic methods are constantly being developed to access these valuable compounds. This Review summarizes recent catalytic approaches towards preparation of trifluoromethyl ethers. Alkene, allylic, benzylic, and aryl trifluoromethoxylation reactions are discussed herein.

Entities:  

Keywords:  Fluorine; Photoredox catalysis; Radical; Transition metal catalysis; Trifluoromethoxylation

Year:  2018        PMID: 30906076      PMCID: PMC6425975          DOI: 10.1016/j.tet.2018.09.020

Source DB:  PubMed          Journal:  Tetrahedron        ISSN: 0040-4020            Impact factor:   2.457


  6 in total

Review 1.  Synthesis of Tri- and Difluoromethoxylated Compounds by Visible-Light Photoredox Catalysis.

Authors:  Johnny W Lee; Katarzyna N Lee; Ming-Yu Ngai
Journal:  Angew Chem Int Ed Engl       Date:  2019-05-28       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.  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

4.  Highly-chemoselective step-down reduction of carboxylic acids to aromatic hydrocarbons via palladium catalysis.

Authors:  Chengwei Liu; Zhi-Xin Qin; Chong-Lei Ji; Xin Hong; Michal Szostak
Journal:  Chem Sci       Date:  2019-04-29       Impact factor: 9.825

5.  Selective C-H trifluoromethoxylation of (hetero)arenes as limiting reagent.

Authors:  Zhijie Deng; Mingxin Zhao; Feng Wang; Pingping Tang
Journal:  Nat Commun       Date:  2020-05-22       Impact factor: 14.919

6.  Nucleophilic trifluoromethoxylation of alkyl halides without silver.

Authors:  Yan Li; Yang Yang; Jinrui Xin; Pingping Tang
Journal:  Nat Commun       Date:  2020-02-06       Impact factor: 14.919

  6 in total

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