Issue 20, 1981

Solvolysis of syn- and anti-N-chloro-1,4-dihydro-1,4-iminonaphthalenes

Abstract

The configuration of chlorine determines the course of methanolysis of the title compounds; new structures are assigned to the reaction products and the rates of reaction of the anti-N-chloroamines are shown to vary according to the ability of the substituents in the benzo-ring to encourage benzo-participation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 1028-1030

Solvolysis of syn- and anti-N-chloro-1,4-dihydro-1,4-iminonaphthalenes

M. L. Durrant and J. R. Malpass, J. Chem. Soc., Chem. Commun., 1981, 1028 DOI: 10.1039/C39810001028

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