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• W2893990985 abstract "A novel rearrangement reaction based on the structure of N-fluoro-N-alkyl benzenesulfonamide was developed. The reaction proceeded readily at 50 °C in formic acid and generated a variety of benzenesulfonamides and aldehydes or ketones simultaneously. The reaction mechanism is believed to be a concerted mechanism that consist of 1,2-aryl migration with the departure of fluorine anion via an SN2 mechanism. This rearrangement reaction features an interesting reaction mechanism, mild reaction conditions, simple operations, and a broad substrate scope." @default.
• W2893990985 created "2018-10-05" @default.
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• W2893990985 date "2018-09-27" @default.
• W2893990985 modified "2023-10-09" @default.
• W2893990985 title "Rearrangement Reaction Based on the Structure of <i>N</i>-Fluoro-<i>N</i>-alkyl Benzenesulfonamide" @default.
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• W2893990985 doi "https://doi.org/10.1021/acs.joc.8b01841" @default.
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