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:
Oxidation of 3-arylisochromans by dimethyldioxirane. An easy route to substituted 3-arylisocoumarins
[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]
Acyl cyanides as carbonyl heterodienophiles
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]
Acyl cyanides as carbonyl heterodienophiles
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]
Acyl cyanides as carbonyl heterodienophiles
[Connors, Richard; Durst, Tony Tetrahedron Letters, 1992 , vol. 33, # 48 p. 7277 - 7280]