Strategies and methods for the attachment of amino acids and peptides to chiral [n]polynorbornane templates

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dc.contributor.authorPfeffer, F.
dc.contributor.authorRussell, R.
dc.date.issued2003
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.identifier.citationOrganic and Biomolecular Chemistry, 2003; 1(11):1845-1851
dc.identifier.doi10.1039/b301980b
dc.identifier.issn1477-0520
dc.identifier.issn1477-0539
dc.identifier.urihttp://hdl.handle.net/2440/48107
dc.language.isoen
dc.publisherRoyal Soc Chemistry
dc.source.urihttps://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
pubs.publication-statusPublished

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