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- W2949989328 abstract "The alkylation of phenol with camphene in the presence of boron trifluoride in glacial acetic acid was accompanied by tandem molecular rearrangement with formation of a mixture of ortho- and para-substituted phenols having 1,7,7-trimethylbicyclo[2.2.1]hept-exo-2-yl and 5,5,6-trimethylbicyclo[2.2.1]hept-exo-2-yl substituents. The same products were obtained by rearrangement of 1,7,7-trimethylbicyclo[2.2.1]hept-exo-2-yloxybenzene under analogous conditions. Similar reactions performed in the presence of aluminum phenoxide as catalyst resulted in predominant formation of the corresponding ortho-substituted phenols." @default.
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- W2949989328 date "2009-01-06" @default.
- W2949989328 modified "2023-10-05" @default.
- W2949989328 title "ChemInform Abstract: Tandem Molecular Rearrangement in the Alkylation of Phenol with Camphene." @default.
- W2949989328 cites W1982231369 @default.
- W2949989328 doi "https://doi.org/10.1002/chin.200901196" @default.
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