Issue 19, 1976

Photocyclization of NN-disubstituted benzoylacetamides and acetoacetamides

Abstract

NN-Dialkyl-benzoylacetamides (1a–e and j–n) and -acetoacetamides (1f–i), and N-methylbenzoylacetanilide (1o) undergo photocyclization involving δ-hydrogen abstraction by the ketone carbonyl group to give N-substituted 4-hydroxypyrrolidin-2-ones (2a–o) in high yields.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 2054-2057

Photocyclization of NN-disubstituted benzoylacetamides and acetoacetamides

T. Hasegawa, H. Aoyama and Y. Omote, J. Chem. Soc., Perkin Trans. 1, 1976, 2054 DOI: 10.1039/P19760002054

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