Journal of the Chemical Society. Chemical communications p. 1496 - 1497 (1984)
Update date:2022-08-16
Topics:
Jefford, Charles W.
Rossier, Jean-Claude
Kohmoto, Shigeo
Boukouvalas, John
The acid-catalysed cleavage of 1,4-dimethyl-1,4-dihydronaphthalene-1,4-endoperoxide gives the 4-hydroxy, methoxy, trifluoroacetoxy, formyloxy, bromo, and chloro methyl derivatives of 1-methylnaphthalene in yields of 36, 38, 52, 76, 77, and 100percent respectively when water, methanol, trifluoroacetic, formic, hydrobromic, or hydrochloric acids are used as reagents.
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