This reaction demonstrates radical addition and hemiaminalization in synthesizing difluoro compounds, suggesting significant pharmaceutical potential.
A new photoredox-catalyzed cascade was accomplished by taking advantage of the bifunctional reactivity of bromodifluoroacetamide with cinnamaldehydes, enabling rapid construction of structurally diverse and highly functionalized difluoro-5-hydroxypyrrolidin-2-ones with excellent chemo- and regio-selectivity. Notably, this transformation proceeds a well-designed tandem process involving sequential regioselective radical addition and challenging hemiaminalization. This strategy provides an innovative modular approach to assemble rarely accessed difluoro-γ-hemiaminal heterocyclic scaffolds, which would facilitate further exploration of their pharmaceutical applications.
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Yan et al. (2025) studied this question.
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