Journal of Organic Chemistry p. 3816 - 3820 (1990)
Update date:2022-07-29
Topics:
Sugimoto, Toshiya
Nojima, Masatomo
Kusabayashi, Shigekazu
The ozonolysis of 1-methylacenaphthylene (1b) and acenaphthylene (1c) 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
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Doi:10.1021/om200135u
(2011)Doi:10.1039/c8ra06148c
(2018)Doi:10.1063/1.457798
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(2005)
