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- W4308584770 abstract "C–F bonds of acyl fluorides can be cleaved and added across teth-ered alkenes in the presence of a cationic rhodium(I) tetrafluorobo-rate catalyst. This 1,2-carbofluorination reaction offers a powerful method for the synthesis of tertiary alkyl fluoride derivatives with atom economy of 100%. Mechanistic studies indicate that the concerted action of a rhodium cation and a tetrafluoroborate anion is the key for the success of this catalytic cleavage and formation of C–F bonds in a controlled manner." @default.
- W4308584770 created "2022-11-12" @default.
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- W4308584770 date "2022-11-08" @default.
- W4308584770 modified "2023-10-17" @default.
- W4308584770 title "Cationic Rhodium(I) Tetrafluoroborate-Catalyzed Intramolecular Carbofluorination of Alkenes via the Activation of a Carbon–Fluorine Bond in Acyl Fluorides" @default.
- W4308584770 doi "https://doi.org/10.26434/chemrxiv-2022-2rrsc" @default.
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