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

Anne Marie Alexander, Marc Bria, Gunther Brunklaus, Stuart Caldwell, Graeme Cooke, James F. Garety, Shanika G. Hewage, Yann Hocquel, Niall McDonald, Gouher Rabani, Georgina Rosair, Brian O. Smith, Hans Wolfgang Spiess, Vincent M. Rotello, Patrice Woisel

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15 Citations (Scopus)

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. © The Royal Society of Chemistry.

Original languageEnglish
Pages (from-to)2246-2248
Number of pages3
JournalChemical Communications
Issue number22
DOIs
Publication statusPublished - 2007

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    Alexander, A. M., Bria, M., Brunklaus, G., Caldwell, S., Cooke, G., Garety, J. F., Hewage, S. G., Hocquel, Y., McDonald, N., Rabani, G., Rosair, G., Smith, B. O., Spiess, H. W., Rotello, V. M., & Woisel, P. (2007). Probing the solvent-induced tautomerism of a redox-active ureidopyrimidinone. Chemical Communications, (22), 2246-2248. https://doi.org/10.1039/b703070c