Issue 0, 1972
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Studies on heterocyclic chemistry. Part XIII. Cleavage of 5-benzyl-amino-oxazoles, photoproducts of N-benzyl-2H-azirine-2-carboxamides, by dialkyl phosphite

Tarozaemon Nishiwaki  and  Fusako Fujiyama  

Abstract

N-Benzyl-2H-azirine-2-carboxamides were prepared by the photochemical or thermal isomerisation of 5-benzyl-aminoisoxazoles. Photochemical reaction of the 2H-azirines in dialkyl phosphite afforded benzamido-N-benzyl-acetamides via 5-benzylamino-oxazoles.

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Article information

DOI
https://doi.org/10.1039/P19720001456
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1456-1459

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Studies on heterocyclic chemistry. Part XIII. Cleavage of 5-benzyl-amino-oxazoles, photoproducts of N-benzyl-2H-azirine-2-carboxamides, by dialkyl phosphite

T. Nishiwaki and F. Fujiyama, J. Chem. Soc., Perkin Trans. 1, 1972, 1456 DOI: 10.1039/P19720001456

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