A novel route to resorcinols
Abstract
Hydroxylation of para-alkylated or 2,6-dialkylated phenols by hydrogen peroxide in SbF5–HF yields resorcinols, the electrophile reacting with the O-protonated substrate.
Hydroxylation of para-alkylated or 2,6-dialkylated phenols by hydrogen peroxide in SbF5–HF yields resorcinols, the electrophile reacting with the O-protonated substrate.
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J. Gesson, J. Jacquesy and M. Jouannetaud, J. Chem. Soc., Chem. Commun., 1980, 1128 DOI: 10.1039/C39800001128
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