Selective Defluoroallylation of Trifluoromethylarenes.
Chaosheng LuoJeffrey S BandarPublished in: Journal of the American Chemical Society (2019)
We report a fluoride-initiated coupling reaction between trifluoromethylarenes and allylsilanes to access allylated α,α-difluorobenzylic compounds. This method's utility is demonstrated through a 30 mmol scale reaction, a sequential allylation/derivatization protocol and multiple examples of site-selective trifluoromethylarene allylation. Initial mechanistic studies suggest a base-induced single electron transfer pathway is responsible for the high efficiency and selectivity of this novel C-F substitution process.
Keyphrases
- electron transfer
- high efficiency
- high glucose
- randomized controlled trial
- ms ms
- diabetic rats
- drinking water
- high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- simultaneous determination
- drug induced
- liquid chromatography
- tandem mass spectrometry
- endothelial cells
- room temperature
- gas chromatography
- structural basis
- ultra high performance liquid chromatography
- high resolution mass spectrometry