Literature DB >> 30640337

Difluorocarbene-derived trifluoromethylselenolation of benzyl halides.

Xin-Lei Chen1, Sheng-Hua Zhou, Jin-Hong Lin, Qing-Hai Deng, Ji-Chang Xiao.   

Abstract

Cu-Promoted difluorocarbene-derived trifluoromethylselenolation of benzyl halides with the Ph3P+CF2CO2-/Se/F- system is described. Three new carbon-heteroatom bonds, a Se-CF2 bond, SeCF2-F bond, and C-SeCF3 bond, were sequentially formed in the reaction. This work represents the first trifluoromethylselenolation protocol involving an external fluoride for the generation of the key intermediate, CF3Se- anion.

Entities:  

Year:  2019        PMID: 30640337     DOI: 10.1039/c8cc09719d

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


  2 in total

Review 1.  Copper-promoted/copper-catalyzed trifluoromethylselenolation reactions.

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

2.  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

  2 in total

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