Issue 0, 1986

Photocyclization of NN-dialkyl β,γ-unsaturated amides. 1,6-Hydrogen transfer via charge-transfer states

Abstract

NN-Dibenzyl and NN-diallyl β,γ-unsaturated amides undergo cyclization on irradiation to give the corresponding pyrrolidin-2-ones via 1,6-hydrogen transfer from the singlet states. The reaction is presumed to involve charge transfer from the amide group to the excited styrene moiety.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1986, 1165-1169

Photocyclization of NN-dialkyl β,γ-unsaturated amides. 1,6-Hydrogen transfer via charge-transfer states

H. Aoyama, Y. Arata and Y. Omote, J. Chem. Soc., Perkin Trans. 1, 1986, 1165 DOI: 10.1039/P19860001165

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