Literature DB >> 25675984

Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate.

Quentin Lefebvre1, Roman Pluta, Magnus Rueping.   

Abstract

The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction.

Entities:  

Year:  2015        PMID: 25675984     DOI: 10.1039/c4cc10212f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  Electrophilic trifluoromethylselenolation of terminal alkynes with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate.

Authors:  Clément Ghiazza; Anis Tlili; Thierry Billard
Journal:  Beilstein J Org Chem       Date:  2017-12-07       Impact factor: 2.883

2.  Electrophilic Trifluoromethylselenolation of Boronic Acids.

Authors:  Clément Ghiazza; Anis Tlili; Thierry Billard
Journal:  Molecules       Date:  2017-05-19       Impact factor: 4.411

Review 3.  Copper-promoted/copper-catalyzed trifluoromethylselenolation reactions.

Authors:  Clément Ghiazza; Anis Tlili
Journal:  Beilstein J Org Chem       Date:  2020-03-03       Impact factor: 2.883

4.  Markovnikov-Type Hydrotrifluoromethylchalcogenation of Unactivated Terminal Alkenes with [Me4N][XCF3] (X = S, Se) and TfOH.

Authors:  Jin Shi; Cheng-Pan Zhang
Journal:  Molecules       Date:  2020-10-03       Impact factor: 4.411

  4 in total

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