Studies on heterocyclic chemistry. Part XIII. Cleavage of 5-benzyl-amino-oxazoles, photoproducts of N-benzyl-2H-azirine-2-carboxamides, by dialkyl phosphite
- 1 January 1972
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- p. 1456-1459
- https://doi.org/10.1039/p19720001456
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.Keywords
This publication has 0 references indexed in Scilit: