Issue 13, 1975

Reactivity of arylolefin excited states. Substituent effects on the photochemical hydrogen migration in 1,1-diarylpropenes

Abstract

Electron-withdrawing substituents increase the rate of photochemical cyclopropane formation from 1,1-diarylpropenes while electron-donating substituents have a retarding effect.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 515-516

Reactivity of arylolefin excited states. Substituent effects on the photochemical hydrogen migration in 1,1-diarylpropenes

S. S. Hixson, J. Chem. Soc., Chem. Commun., 1975, 515 DOI: 10.1039/C39750000515

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