Issue 22, 1996

Highly diastereoselective photooxygenation of chiral 1,2-dihydronaphthalenes: evidence for a common intermediate in the ene reaction and the [4 + 2] cycloaddition

Abstract

The photooxygenation of chiral 1,2-dihydronaphthalenes exhibits a very high degree of stereoselectivity, which provides evidence for a common intermediate with perepoxide geometry.

Article information

Article type
Paper

Chem. Commun., 1996, 2585-2586

Highly diastereoselective photooxygenation of chiral 1,2-dihydronaphthalenes: evidence for a common intermediate in the ene reaction and the [4 + 2] cycloaddition

T. Linker, F. Rebien and G. Tóth, Chem. Commun., 1996, 2585 DOI: 10.1039/CC9960002585

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