Issue 0, 1981

Iminyls. Part 9. Intramolecular addition of an iminyl to an alkene

Abstract

Phenyl o-styrylphenyl iminyl, generated by oxidation of the corresponding O-carboxymethyloxime with persulphate and by thermolysis of the perester of that acid, cyclises to give a mixture of isoquinoline and 1H-isoindole derivatives. The intermediate radicals have been investigated by e.s.r.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 1721-1724

Iminyls. Part 9. Intramolecular addition of an iminyl to an alkene

S. Atmaram, A. R. Forrester, M. Gill and R. H. Thomson, J. Chem. Soc., Perkin Trans. 1, 1981, 1721 DOI: 10.1039/P19810001721

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