Issue 12, 1984

Effect of para-substituents on the photochemical ring-opening reactivity of 1-(p-substituted-benzoyl)aziridines in methanol

Abstract

Photolysis of 1-(p-substituted-benzoyl)aziridines (1ae) in Ar-purged methanol led to N-(2-methoxyethyl)benzamides (3be) as the methanolysis products and/or N-ethylbenzamides (2a and b). Penta-1,3-diene quenched the formation of (2a and b) but not (3be).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1984, 1959-1961

Effect of para-substituents on the photochemical ring-opening reactivity of 1-(p-substituted-benzoyl)aziridines in methanol

S. Nishimoto, T. Izukawa, Y. Haruta and T. Kagiya, J. Chem. Soc., Perkin Trans. 2, 1984, 1959 DOI: 10.1039/P29840001959

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