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

Publication details

The article was received on 01 Mar 2007, accepted on 27 Apr 2007 and first published on 09 May 2007


Article type: Communication
DOI: 10.1039/B703070C
Citation: Chem. Commun., 2007,0, 2246-2248
  •   Request permissions

    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, 0, 2246
    DOI: 10.1039/B703070C

Search articles by author

Spotlight

Advertisements