Research demonstrates chemoselective hydrodefluorination of trifluoroacetamides, suggesting wavelength tuning impacts the SET/EDA pathway.
A chemoselective hydrodefluorination of trifluoroacetamides enabled by switching the SET/EDA pathway through simply tuning the wavelength of irradiation, delivering the corresponding CFH 2 and CF 2 H analogues selectively.
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Guo et al. (2025) studied this question.
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