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- W4248932365 abstract "Chlorination of 6-chloro-4-cyclohexylresorcinol with sulfuryl chloride gives an unstable intermediate (I), possessing one phenolic hydroxyl radical. Its methylation with diazomethane, followed by catalytic reduction results in the formation of a mono-methyl ether (V) of 6-chloro-4-cyclohexylresorcinol. In order to determine the relative positions of the phenolic hydroxyl and the methoxyl group in (V), various reactions were carried out from which (V) was assumed to be 6-chloro-4-cyclohexylresorcinol-3-methyl ether, showing the phenolic hydroxyl to be present in the 1-position and the methoxyl at 3-position." @default.
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- W4248932365 date "1952-01-01" @default.
- W4248932365 modified "2023-10-07" @default.
- W4248932365 title "Synthetic Studies of Anthelmintics. XII" @default.
- W4248932365 doi "https://doi.org/10.1248/yakushi1947.72.7_858" @default.
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