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- W2158451293 abstract "Trifluoroethylation: Aryl boronic acids can be catalytically trifluoroethylated with the readily available reagent CF3CH2I (see scheme, dba=dibenzylideneacetone). The reaction tolerates a variety of functional groups and can be extended to the trifluoroethylation of aryl or alkenyl boronic esters. The method is also suitable for the late-stage installation of the CF3CH2 group into target molecules. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2158451293 created "2016-06-24" @default.
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- W2158451293 date "2011-12-13" @default.
- W2158451293 modified "2023-10-07" @default.
- W2158451293 title "Palladium-Catalyzed 2,2,2-Trifluoroethylation of Organoboronic Acids and Esters" @default.
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- W2158451293 doi "https://doi.org/10.1002/anie.201106742" @default.
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