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Cited by 2 publications
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“…Prolonged bromination of 1 in presence of iron gave the 2,3,4,5-tetrabromo derivative. The position of the bromine atoms has not been definitely determined [ 117 ]. On the other hand, treatment of 1 with bromine in chlorobenzene as a solvent gave 1,8-naphthalic anhydride whereas the reaction did not take place in nitrobenzene [ 118 ].…”
Section: Reactions Of Acenaphthenequinonesmentioning
confidence: 99%
“…Prolonged bromination of 1 in presence of iron gave the 2,3,4,5-tetrabromo derivative. The position of the bromine atoms has not been definitely determined [ 117 ]. On the other hand, treatment of 1 with bromine in chlorobenzene as a solvent gave 1,8-naphthalic anhydride whereas the reaction did not take place in nitrobenzene [ 118 ].…”
Section: Reactions Of Acenaphthenequinonesmentioning
confidence: 99%
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