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dc.contributor.authorWilkinson, Brendanen_US
dc.contributor.authorBornaghi, Laurenten_US
dc.contributor.authorLopez, Marieen_US
dc.contributor.authorHealy, Peteren_US
dc.contributor.authorPoulsen, Sally-Annen_US
dc.contributor.authorHouston, Todden_US
dc.date.accessioned2017-04-24T08:40:41Z
dc.date.available2017-04-24T08:40:41Z
dc.date.issued2010en_US
dc.date.modified2010-09-01T08:07:38Z
dc.identifier.issn00049425en_US
dc.identifier.doi10.1071/CH09426en_AU
dc.identifier.urihttp://hdl.handle.net/10072/32201
dc.description.abstractWe have developed an efficient synthesis of N-propargyl iminosugars for use in diversity-oriented library development. Through a common, crystalline intermediate both piperidine and azepane scaffolds can be prepared with an alkyne functional group, allowing for further elaboration through reaction with azides.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherCSIRO Publishingen_US
dc.publisher.placeAustraliaen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom821en_US
dc.relation.ispartofpageto829en_US
dc.relation.ispartofissue5en_US
dc.relation.ispartofjournalAustralian Journal of Chemistryen_US
dc.relation.ispartofvolume63en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchBiologically Active Moleculesen_US
dc.subject.fieldofresearchcode030401en_US
dc.titleSynthesis of N-Propargyl Iminosugar Scaffolds for Compound Library Generation using Click Chemistryen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyGriffith Sciences, School of Natural Sciencesen_US
gro.date.issued2010
gro.hasfulltextNo Full Text


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