Issue 18, 2001

Oxidative radical cyclizations of malonate enolates induced by the ferrocenium ion – a remarkable influence of enolate counterion and additives

Abstract

To generalize oxidative radical cyclizations of malonate enolates induced by recyclable single electron transfer (SET) oxidant ferrocenium hexafluorophosphate 1, the reactivity of a series of enolates 3 that differ only in their counterions was studied. Only lithium enolates were oxidized by 1, irrespective of their generation method. The presence of amines in stoichiometric or substoichiometric amounts is necessary for SET oxidation–bicyclization of Na, K, Mg, Zn, Si, or Ti enolates 3. The nucleophilicity of 3, the amine, and the presence of halide ions determine the bicyclization yield of lactone 7.

Graphical abstract: Oxidative radical cyclizations of malonate enolates induced by the ferrocenium ion – a remarkable influence of enolate counterion and additives

Article information

Article type
Paper
Submitted
07 Mar 2001
Accepted
20 Jul 2001
First published
24 Aug 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 2277-2282

Oxidative radical cyclizations of malonate enolates induced by the ferrocenium ion – a remarkable influence of enolate counterion and additives

U. Jahn and P. Hartmann, J. Chem. Soc., Perkin Trans. 1, 2001, 2277 DOI: 10.1039/B102211N

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