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dc.contributor.authorGemma, Emiliano*
dc.contributor.authorHulme, Alison N*
dc.contributor.authorJahnke, Astrid*
dc.contributor.authorJin, Lan*
dc.contributor.authorLyon, Malcolm*
dc.contributor.authorMüller, Ralf M*
dc.contributor.authorUhrín, Dusan*
dc.date.accessioned2009-06-15T12:28:12Z
dc.date.available2009-06-15T12:28:12Z
dc.date.issued2007-07-14
dc.identifier.citationDMT-MM mediated functionalisation of the non-reducing end of glycosaminoglycans. 2007 (26):2686-8 Chem. Commun.en
dc.identifier.issn1359-7345
dc.identifier.pmid17594020
dc.identifier.doi10.1039/b617038b
dc.identifier.urihttp://hdl.handle.net/10541/70477
dc.description.abstractEfficient functionalisation of the non-reducing end of uronic acid derivatives and glycosaminoglycan-derived disaccharides using peptide coupling has been achieved, mediated by the water-soluble agent DMT-MM.
dc.language.isoenen
dc.subject.meshChromatography, High Pressure Liquid
dc.subject.meshGlycosaminoglycans
dc.subject.meshMagnetic Resonance Spectroscopy
dc.subject.meshModels, Molecular
dc.subject.meshMorpholines
dc.subject.meshOxidation-Reduction
dc.titleDMT-MM mediated functionalisation of the non-reducing end of glycosaminoglycansen
dc.typeArticleen
dc.contributor.departmentSchool of Chemistry, University of Edinburgh, West Mains Road, Edinburgh, UK EH9 3JJ.en
dc.identifier.journalChemical Communicationsen
html.description.abstractEfficient functionalisation of the non-reducing end of uronic acid derivatives and glycosaminoglycan-derived disaccharides using peptide coupling has been achieved, mediated by the water-soluble agent DMT-MM.


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