Abstract
The ozonolysis of title compound in carbon tetrachloride, acetonitrile, acetic acid, and trifluoroethanol revealed that the ozonide yield was much higher in reactions in protic solvents than in aprotic solvents. Such an assistance of the protic solvents on the ozonide formation was not observed in the case of the more bulky 1-phenylacenaphthylene
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