Issue 7, 2004

Relative reactivity of three and four membered rings – the absence of charge effect

Abstract

Radical (neutral) and electrophilic (cationic) ring opening reactions were studied computationally in order to probe the difference in reactivity between three and four membered rings. Using the Marcus equation we have shown that the activation energy for the four membered ring opening is close to the Marcus predicted barrier whereas three membered rings display much higher reactivity than that predicted by the Marcus equation. Thus, the reactivity of the three membered rings is enhanced, in addition to the strain release, by another factor which is not operative in the four membered rings. It is clear also that this factor is not charge dependent. The possible origin of this effect is discussed.

Graphical abstract: Relative reactivity of three and four membered rings – the absence of charge effect

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2003
Accepted
12 Feb 2004
First published
08 Mar 2004

Org. Biomol. Chem., 2004,2, 1065-1069

Relative reactivity of three and four membered rings – the absence of charge effect

J. L. Wolk, M. Sprecher, H. Basch and S. Hoz, Org. Biomol. Chem., 2004, 2, 1065 DOI: 10.1039/B314869F

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.

Social activity

Spotlight

Advertisements