89619-71-6Relevant academic research and scientific papers
Ozonolysis of 1-Substituted 2,3-Diphenylindenes and o-(1-Substituted-2-phenyl-3-methoxy-2-propenyl)benzophenones. Remarkable Effects of the Method of Generation of the Carbonyl Oxide Intermediates on the Stereochemistries of Both the Ozonide and the Metha
Nakamura, Norinaga,Fujisaka, Tomohiro,Nojima, Masatomo,Kusabayashi, Shigekazu,McCullough, Kevin J.
, p. 1799 - 1803 (2007/10/02)
Ozonolyses of 1-substituted 2,3-diphenylindenes 1a,b and o-(1-substituted-2-phenyl-3-methoxy-2-propenyl)benzophenones 8a,b in methanol-methylene chloride at -70 deg C, which should proceed through common carbonyl oxide intermediates 11a,b, afforded stereo
Ozonolysis of 1-Methylindenes. Solvent, Temperature, and Substituent Electronic Effects on the Ozonide Exo/Endo Ratio
Miura, Masahiro,Fujisaka, Tomohiro,Nojima, Masatomo,Kusabayashi, Shigekazu,McCullough, Kevin J.
, p. 1504 - 1509 (2007/10/02)
The ozonolyses of 1-methyl-3-aryl-, 1,2-dimethyl-3-aryl-, and 1-methyl-2,3-diarylindenes (1a-e, 4a-e, 7a-e, 7a',b',d') in various solvents at several temperatures have been undertaken.The data revealed the following. (a) The ozonolysis of indenes 1c, 4c,
Unprecedented Solvolytic Diversion of Carbonyl Oxide Intermediates derived from the Ozonolysis of 1-Methyl-2,3-diphenylindene. Isolation and Characterisation of a Novel Solvent-participated Product
McCullough, Kevin J.,Nojima, Masatomo,Miura, Mashiro,Fujisaka, Tomohiro,Kusabayashi, Shigekazu
, p. 35 - 37 (2007/10/02)
Ozonolysis of 1-methyl-2,3-diphenylindene (1) in methylene chloride-methanol at -70 deg C affords a novel alkoxyhydroperoxide product (3), incorporating methanol, whose crystal structure has been established by X-ray analysis.
