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• W2620134880 abstract "Abstract We report a redox‐neutral formylation of aryl chlorides that proceeds through selective 2‐functionalization of 1,3‐dioxolane through nickel and photoredox catalysis. This scalable benchtop approach provides a distinct advantage over traditional reductive carbonylation in that no carbon monoxide, pressurized gas, or stoichiometric reductant is employed. The mild conditions give unprecedented scope from abundant and complex aryl chloride starting materials." @default.
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• W2620134880 date "2017-05-23" @default.
• W2620134880 modified "2023-10-18" @default.
• W2620134880 title "Mild, Redox‐Neutral Formylation of Aryl Chlorides through the Photocatalytic Generation of Chlorine Radicals" @default.
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• W2620134880 doi "https://doi.org/10.1002/anie.201702079" @default.
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