Issue 0, 1972

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

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.

Article information

Article type
Paper

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

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements