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dc.contributor.authorLiakatos, Angelaen_US
dc.contributor.authorKiefel, Miltonen_US
dc.contributor.authorvon Itzstein, Marken_US
dc.contributor.editorAmos B Smith, Carol Carren_US
dc.date.accessioned2017-04-24T07:56:35Z
dc.date.available2017-04-24T07:56:35Z
dc.date.issued2003en_US
dc.date.modified2009-10-19T05:23:48Z
dc.identifier.issn15237060en_US
dc.identifier.doi10.1021/ol035733den_AU
dc.identifier.urihttp://hdl.handle.net/10072/5841
dc.description.abstractA new approach toward the synthesis of lactose-based S-linked sialylmimetics of a(2,3)-linked sialosides is described. These compounds, represented by the general structure 3, were prepared from methyl ߭d-lactoside in 11 steps. It was found that the choice of protecting group was crucial to allow the efficient introduction of sulfur at the 3-position of the galactose ring.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherAmerican Chemical Societyen_US
dc.publisher.placeWashington, DCen_US
dc.publisher.urihttp://pubs.acs.org/journal/orlef7en_AU
dc.relation.ispartofpagefrom4365en_US
dc.relation.ispartofpageto4368en_US
dc.relation.ispartofissue23en_US
dc.relation.ispartofjournalOrganic Lettersen_US
dc.relation.ispartofvolume5en_US
dc.subject.fieldofresearchcode250301en_US
dc.titleSynthesis of lactose-based S-linked sialylmimetics of alpha(2,3)-sialosides.en_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyOffice of the Snr Dep Vice Chancellor, Institute for Glycomicsen_US
gro.rights.copyrightCopyright 2003 American Chemical Society. Self-archiving of the author-manuscript version is not yet supported by this publisher. Please refer to the journal link for access to the definitive, published version or contact the author for more information.en_AU
gro.date.issued2003
gro.hasfulltextNo Full Text


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