Catalytic Asymmetric Synthesis of Tertiary Alkyl Fluorides: Negishi Cross-Couplings of Racemic α,α-Dihaloketones
datasetposted on 17.12.2015, 01:31 by Yufan Liang, Gregory C. Fu
The development of new approaches to the construction of fluorine-containing target molecules is important for a variety of scientific disciplines, including medicinal chemistry. In this Article, we describe a method for the catalytic enantioselective synthesis of tertiary alkyl fluorides through Negishi reactions of racemic α-halo-α-fluoroketones, which represents the first catalytic asymmetric cross-coupling that employs geminal dihalides as electrophiles. Thus, selective reaction of a C–Br (or C–Cl) bond in the presence of a C–F bond can be achieved with the aid of a nickel/bis(oxazoline) catalyst. The products of the stereoconvergent cross-couplings, enantioenriched tertiary α-fluoroketones, can be converted into an array of interesting organofluorine compounds.
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electrophilepresenceDihaloketonesTheRacemicgeminal dihalidesenantioenrichedarrayNegishi reactionsdisciplinevarietyTertiary Alkyl FluoridesracemicArticleenantioselective synthesisapproachmethodCatalytic Asymmetric Synthesisstereoconvergentfluoroketonemoleculeconstructioncatalystalkyl fluorideshaloorganofluorine compoundsaidbond