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- W4323854356 abstract "Arynes are highly reactive and versatile intermediates for the functionalization of aromatic rings that are often generated using strong bases or fluoride sources, which in some cases can limit functional group tolerance. Here we demonstrate that triaryl oxonium ions can be transformed into arynes through treatment with solid potassium phosphate at room temperature. A substantial range of functional group-bearing arynes including 4,5-pyrimidynes may be generated and trapped by cycloaddition reactions in high yields. Other arynophiles including nitrones, alkenes, and azides are compatible with these conditions. Quantum computation in conjunction with an intramolecular kinetic isotope study is consistent with an E1cB-like mechanism of elimination to form the aryne. These investigations demonstrate that the oxonium ion is a powerful electron-withdrawing group and a particularly effective leaving group. We anticipate this study will stimulate further investigations into the synthetic utility of aryl oxonium ions." @default.
- W4323854356 created "2023-03-11" @default.
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- W4323854356 date "2023-03-10" @default.
- W4323854356 modified "2023-10-03" @default.
- W4323854356 title "Harnessing triaryloxonium ions for aryne generation" @default.
- W4323854356 doi "https://doi.org/10.26434/chemrxiv-2023-5wwqd" @default.
- W4323854356 hasPublicationYear "2023" @default.
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