Literature DB >> 17979805

alpha-fluorinated ethers as "exotic" entity in medicinal chemistry.

Peter Jeschke1, Eckhard Baston, Frédéric R Leroux.   

Abstract

After nitrogen, fluorine occupies the position of second favorite heteroelement in life science-oriented research. In contrast, the trifluoromethoxy group is still perhaps the least well understood fluorine substituent, although its occurrence has significantly increased in the recent years. Today, significant application areas for trifluoromethoxy substituted pharmaceuticals are in the field of analgesics, anesthetics, cardiovascular drugs, respiratory drugs, psychopharmacologic drugs, neurological drugs, gastrointestinal drugs and anti-infective therapeutics. The present review will give an overlook of its use in medicinal chemistry.

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Year:  2007        PMID: 17979805     DOI: 10.2174/138955707782110150

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  18 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.  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.  Silver-mediated trifluoromethoxylation of aryl stannanes and arylboronic acids.

Authors:  Chenghong Huang; Theresa Liang; Shinji Harada; Eunsung Lee; Tobias Ritter
Journal:  J Am Chem Soc       Date:  2011-08-09       Impact factor: 15.419

7.  Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives.

Authors:  Pengju Feng; Ming-Yu Ngai
Journal:  J Vis Exp       Date:  2016-01-19       Impact factor: 1.355

8.  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

9.  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

10.  Trifluoromethyl ethers--synthesis and properties of an unusual substituent.

Authors:  Frédéric R Leroux; Baptiste Manteau; Jean-Pierre Vors; Sergiy Pazenok
Journal:  Beilstein J Org Chem       Date:  2008-04-29       Impact factor: 2.883

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