Issue 15, 1977

Reaction of singlet oxygen with hindered olefins: evidence for a perepoxide intermediate

Abstract

Isolation, along with expected product, of 1,2-dioxolans of rearranged skeleton from the reaction of singlet oxygen with certain hindered alkenes suggest the intermediacy of a dipolar species such as a perepoxide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 517-518

Reaction of singlet oxygen with hindered olefins: evidence for a perepoxide intermediate

F. McCapra and I. Beheshti, J. Chem. Soc., Chem. Commun., 1977, 517 DOI: 10.1039/C39770000517

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