Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.13/33618
- Title
- Identification of aminopyrimidine regioisomers via line broadening effects in ¹H and ¹³C NMR spectroscopy
- Author/Creator
-
Garner, James;
Hill, Tim;
Odell, Luke;
Keller, Paul;
Morgan, Jody;
McCluskey, Adam
- Institution
- The University of Newcastle. Faculty of Science & Information Technology, School of Environmental and Life Science
- Description
- Substituted mono- and diamino-pyrimidines were synthesized as part of our medicinal chemistry programmes. Primary amines substituted at the 4-position exhibited room-temperature line broadening effects in both ¹H and ¹³C NMR spectroscopy due to the presence of rotamers, but these effects were not observed for substituents in the 2-position. This provided a simple diagnostic tool for the identification of regioisomers, a determination which would otherwise have required two-dimensional experiments.
- Relation
- Australian Journal of Chemistry Vol. 57, Issue 11, p. 1079-1083
- Publisher Link
- http://dx.doi.org/10.1071/CH03316
- Date
- 2004
- Publisher
- CSIRO Publishing
- Keyword(s)
-
mono-pyrimidines;
diamino-pyrimidines;
amines;
¹H and ¹³C NMR spectroscopy;
regioisomers
- Resource Type
- journal article
- Identifier
- http://hdl.handle.net/1959.13/33618
- Identifier
- ISSN:0004-9425
- Reviewed

26 Visitors
32 Hits
0 Downloads