Literature DB >> 30372065

Cobalt-Catalyzed Trifluoromethoxylation of Epoxides.

Jie Liu1, Yongliang Wei1, Pingping Tang1,2.   

Abstract

A catalytic ring-opening reaction of epoxides by nucleophilic trifluoromethoxylation of trifluoromethyl arylsulfonate has been developed based on the use of a cobalt catalyst. This reaction provides an efficient, simple route for directly construction of a wide range of vicinal trifluoromethoxyhydrins under mild conditions. In addition, this method can convert terminal epoxides into target products with good chemo- and regioselectivity.

Entities:  

Year:  2018        PMID: 30372065     DOI: 10.1021/jacs.8b10298

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  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

2.  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

  2 in total

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