Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/48107
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dc.contributor.authorPfeffer, F.-
dc.contributor.authorRussell, R.-
dc.date.issued2003-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2003; 1(11):1845-1851-
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttp://hdl.handle.net/2440/48107-
dc.description© The Royal Society of Chemistry 2003-
dc.description.abstractA versatile synthesis of amino acid and peptide functionalised [n]polynorbornane scaffolds is described. The frameworks are constructed using the stereoselective and regioselective cycloaddition of suitably functionalisedchiral cyclobutene epoxides with similar norbornenes. The strategies employed allow a range of topologies to be accessed and a number of regioselectively addressable linkage points to be accommodated.-
dc.language.isoen-
dc.publisherRoyal Soc Chemistry-
dc.source.urihttp://dx.doi.org/10.1039/b301980b-
dc.subjectNorbornanes-
dc.subjectAmino Acids-
dc.subjectPeptides-
dc.subjectCyclization-
dc.subjectStereoisomerism-
dc.titleStrategies and methods for the attachment of amino acids and peptides to chiral [n]polynorbornane templates-
dc.typeJournal article-
dc.identifier.doi10.1039/b301980b-
pubs.publication-statusPublished-
Appears in Collections:Adelaide Graduate Centre publications
Aurora harvest 6

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