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- W2912441140 endingPage "3922" @default.
- W2912441140 startingPage "3918" @default.
- W2912441140 abstract "A novel strategy for the expedient construction of CF3-embeded tertiary/quarternary carbon centers was developed by taking advantage of photoredox catalysis. Thanks to a key step of single-electron oxidation, electron-rich gem-difluoroalkenes, which otherwise are essentially reluctant towards F-nucleoplilic addition, now readily participate in this fluoroallylation reaction. Furthermore, this strategy provides an elegant example for the generation, as well as functionalization, of α-CF3-substituted benzylic radical intermediates using cheap and readily available starting materials." @default.
- W2912441140 created "2019-02-21" @default.
- W2912441140 creator A5004206321 @default.
- W2912441140 creator A5024080175 @default.
- W2912441140 creator A5077423550 @default.
- W2912441140 creator A5084548935 @default.
- W2912441140 creator A5029965098 @default.
- W2912441140 date "2019-03-18" @default.
- W2912441140 modified "2023-10-05" @default.
- W2912441140 title "Photoredox‐Coupled F‐Nucleophilic Addition: Allylation of <i>gem</i> ‐Difluoroalkenes" @default.
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- W2912441140 doi "https://doi.org/10.1002/anie.201814308" @default.