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dc.contributor.authorHouston, Todden_US
dc.contributor.authorKoreeda, Masatoen_US
dc.date.accessioned2017-04-24T11:09:37Z
dc.date.available2017-04-24T11:09:37Z
dc.date.issued2009en_US
dc.date.modified2010-06-25T07:01:57Z
dc.identifier.issn00086215en_US
dc.identifier.doi10.1016/j.carres.2009.08.026en_AU
dc.identifier.urihttp://hdl.handle.net/10072/30632
dc.description.abstractIodine not only promotes smooth ߭selective glycosylation of ribose tetra-acetate under exceptionally mild conditions, it also catalyzes an expedient acetonide-forming reaction in this system when dry acetone is used as a solvent.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherElsevieren_US
dc.publisher.placeUKen_US
dc.publisher.urihttp://www.sciencedirect.com/science/journal/00086215en_AU
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom2240en_US
dc.relation.ispartofpageto2244en_US
dc.relation.ispartofissue16en_US
dc.relation.ispartofjournalCarbohydrate Researchen_US
dc.relation.ispartofvolume344en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchOrganic Chemical Synthesisen_US
dc.subject.fieldofresearchcode030503en_US
dc.titleIodine-promoted ribosylation leads to a facile acetonide-forming reactionen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2009
gro.hasfulltextNo Full Text


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