Ozonolysis of acenaphthylene and 1-substituted acenaphthylenes

descriptionPublicationkeyboard_double_arrow_right Article 01 Jun 1990 English Publisher:American Chemical Society (ACS)Journal:The Journal of Organic Chemistry, volume 55, pages 3,816-3,820 (issn: 0022-3263, eissn: 1520-6904,

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Authors: Toshiya Sugimoto; Masatomo Nojima; Shigekazu Kusabayashi;

doi: 10.1021/jo00299a024

Ozonolysis of acenaphthylene and 1-substituted acenaphthylenes

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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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