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Selective nickel-catalyzed fluoroalkylations of olefins
Ist Teil von
Chemical communications (Cambridge, England), 2020-12, Vol.56 (96), p.15157-1516
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2020
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Mild and selective nickel-catalyzed trifluoromethylation and perfluoroalkylation reactions of alkenes were developed to provide fluorinated olefins, including natural products, pharmaceuticals, and variety of synthetic building blocks in good to excellent yields (38 examples). Control experiments, kinetic measurements and
in situ
EPR studies reveal the importance of radical species and the formation of 1,2-adducts as intermediates.
Fluoroalkylated olefins made easy: a mild and selective Ni-catalyzed fluoroalkylation including trifluoromethylation of alkenes was developed. Various fluorinated olefins were provided in good to excellent yields.