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
Full Text: HTML
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 ...
Related Articles:
[Bovicelli, Paolo; Lupattelli, Paolo; Crescenzi, Benedetta; Sanetti, Anna; Bernini, Roberta Tetrahedron, 1999 , vol. 55, # 51 p. 14719 - 14728]
[v. Auwers; Auffenberg Chemische Berichte, 1919 , vol. 52, p. 111]
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]