Herein, we report a photoinduced electron donor-acceptor (EDA) complex-mediated strategy for the aminomethylation of gem-difluoroalkenes using α-amino acid-derived N-hydroxyphthalimide (NHPI) esters. This method facilitates the efficient synthesis of diverse β,β-difluoroamines under mild conditions, demonstrating a broad substrate scope with excellent functional group compatibility. Systematic mechanistic studies elucidate a photocatalyst-enhanced EDA-enabled radical pathway. Significantly, the synthetic utility of this strategy is further exemplified by its successful extension to hydroxyl- and thiol-methylation reactions, delivering a range of β,β-difluoroalcohol and β,β-difluorothiol derivatives in high yields.
Dong et al. (Thu,) studied this question.
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