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- W4323838504 abstract "A visible-light-induced acyl radical conjugate addition to electron-deficient alkenes with acylsilane was realized by merging photoredox and Lewis acid catalysis under mild reaction conditions. Various tri- and tetra-substituted furans were obtained with good yield (up to 97%) from α,β-unsaturated ketones. Based on the experimental results and spectral analysis, a possible catalytic cycle involving 1,4-conjugate addition/ring-closure/arylation sequence was proposed. Beyond that, 1,6-acyl radical conjugate addition to para-quinone methides was also accomplished to deliver a series of α-aryl ketones by using this synergistic catalysis protocol." @default.
- W4323838504 created "2023-03-11" @default.
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- W4323838504 date "2023-03-10" @default.
- W4323838504 modified "2023-09-28" @default.
- W4323838504 title "Radical Conjugate Addition of Acylsilane Enabled by Synergistic Photoredox and Lewis Acid Catalysis" @default.
- W4323838504 doi "https://doi.org/10.22541/au.167845529.90801098/v1" @default.
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