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- W2809728529 endingPage "2959" @default.
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- W2809728529 abstract "Sulfoxide-promoted ortho-C–H functionalization reactions of aromatic compounds have emerged as powerful tools for organic synthesis. Among them, [3,3] sigmatropic rearrangement induced by interrupted Pummerer reaction or electrophilic activation of sulfoxides has proved to be a fruitful strategy due to its versatility and high reaction efficiency. This digest paper mainly focuses on recent progress on C–H functionalization reactions of aryl sulfoxides via [3,3] sigmatropic rearrangement of sulfonium-tethered intermediates." @default.
- W2809728529 created "2018-07-10" @default.
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- W2809728529 date "2018-08-01" @default.
- W2809728529 modified "2023-10-16" @default.
- W2809728529 title "Recent development of ortho -C–H functionalization of aryl sulfoxides through [3,3] sigmatropic rearrangement" @default.
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- W2809728529 doi "https://doi.org/10.1016/j.tetlet.2018.06.055" @default.
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