Ozonolysis of 2-phenyl-3-(acyloxy)-1H-indenes and 1-phenyl-2-(benzoyloxy) acenaphthylene. Intramolecular carbonyl oxide-(acyloxy) carbonyl cycloaddition

…, N Nakamura, M Nojima, S Kusabayashi

Index: Sugimoto, Toshiya; Nakamura, Norinaga; Nojima, Masatomo; Kusabayashi, Shigekazu Journal of Organic Chemistry, 1991 , vol. 56, # 4 p. 1672 - 1674

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Citation Number: 4

Abstract

Alkoxy and acyloxy ozonides (3-alkoxy-and 3-(acyloxy)-1, 2, 4-trioxolanes) constitute a new class of cyclic peroxides that have generated much interest. The alkoxy ozonides have been prepared by both intermolecular'and intram~ lecular~~~ cycloaddition of a carbonyl oxide, generated by alkene ozonolysis in solution, to an ester. An alternative method is ozonolysis of vinyl ethers and vinyl acetates on polyethylene. By this method the corresponding ...