Jump to main content
Jump to site search

Issue 22, 2007
Previous Article Next Article

Probing the solvent-induced tautomerism of a redox-active ureidopyrimidinone

Author affiliations

Abstract

A ferrocene-functionalised ureidopyrimidinone has been synthesised that can signal the solvent-induced tautomerism of the dimeric 4[1H]-pyrimidinone form to the monomeric 6[1H]-pyrimidinone form.

Graphical abstract: Probing the solvent-induced tautomerism of a redox-active ureidopyrimidinone

Back to tab navigation

Supplementary files

Article information


Submitted
01 Mar 2007
Accepted
27 Apr 2007
First published
09 May 2007

Chem. Commun., 2007, 2246-2248
Article type
Communication

Probing the solvent-induced tautomerism of a redox-active ureidopyrimidinone

A. Alexander, M. Bria, G. Brunklaus, S. Caldwell, G. Cooke, J. F. Garety, S. G. Hewage, Y. Hocquel, N. McDonald, G. Rabani, G. Rosair, B. O. Smith, H. W. Spiess, V. M. Rotello and P. Woisel, Chem. Commun., 2007, 2246
DOI: 10.1039/B703070C

Social activity

Search articles by author

Spotlight

Advertisements