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- W1972677894 abstract "Electrochemical oxidation of aromatic compounds in the presence of fluoride ion gives products derived from initial oxidation of aromatic substrate and subsequent reaction with fluoride ion. The second of the one-electron transfer steps leads to benzenium ions, which give either fluoroaromatic compounds (elimination) or fluorocyclohexadienes (addition). The elimination of a t-butyl-group during anodic oxidation of p-di-t-butylbenzene yielded p-fluoro-t-butylbenzene. Further examples of the reaction involve p-fluorodiphenyl, p-fluoro-t-butylbenzene, and p-fluorophenol ethers." @default.
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- W1972677894 date "1975-01-01" @default.
- W1972677894 modified "2023-10-18" @default.
- W1972677894 title "Anodic oxidation of p-disubstituted benzenes in the presence of fluoride ion" @default.
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- W1972677894 doi "https://doi.org/10.1016/0040-4020(75)80112-8" @default.
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