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

DOI: 10.1021/ja00187a038

Source and publish data:

Journal of the American Chemical Society p. 1799 - 1803 (1989)

Update date:2022-07-29

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Authors:

Nakamura, Norinaga

Fujisaka, Tomohiro

Nojima, Masatomo

Kusabayashi, Shigekazu

McCullough, Kevin J.

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Article abstract of DOI:10.1021/ja00187a038

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

Full text of DOI:10.1021/ja00187a038

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