Literature DB >> 27571314

Benzyltrifluoromethyl (or Fluoroalkyl) Selenide: Reagent for Electrophilic Trifluoromethyl (or Fluoroalkyl) Selenolation.

Quentin Glenadel1, Ermal Ismalaj1, Thierry Billard1.   

Abstract

Trifluoromethylseleno substituent (CF3Se) is an emerging group, but its direct introduction onto organic molecules is still quite limited and mainly restricted to nucleophilic methods. Herein, we describe a new approach to easily and safely perform electrophilic trifluoromethylselenolation starting from a simple and easily accessible reagent, namely, benzyltrifluoromethyl selenide. This strategy can be generalized to various fluoroalkylselanyl groups, even functionalized ones.

Entities:  

Year:  2016        PMID: 27571314     DOI: 10.1021/acs.joc.6b01344

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  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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