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dc.contributor.authorHuang, Shengshuen_US
dc.contributor.authorYu, Haien_US
dc.contributor.authorChen, Xien_US
dc.date.accessioned2017-05-03T15:55:12Z
dc.date.available2017-05-03T15:55:12Z
dc.date.issued2007en_US
dc.date.modified2011-05-30T06:56:37Z
dc.identifier.issn15213773en_US
dc.identifier.doi10.1002/ange.200604799en_AU
dc.identifier.urihttp://hdl.handle.net/10072/38875
dc.description.abstractGar nicht w䨬erisch: Sialins䵲e-Aldolase aus Escherichia coli erweist sich als ungew樮lich flexibel f철die Umsetzung von Disacchariden, die eine Mannose (Man) oder ein N-Glycolylmannosamin (ManNGc) am reduzierenden Ende tragen, zu den entsprechenden Disacchariden mit einer Desaminoneuramins䵲e (KDN) bzw. einer N-Glycolylneuramins䵲e (Neu5Gc) am reduzierenden Ende (siehe Schema; Gal: Galactose, Glc: Glucose). Die chemoenzymatische Methode ist allgemein anwendbar und effizient.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherWileyen_US
dc.publisher.placeGermanyen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom2249en_US
dc.relation.ispartofpageto2492en_US
dc.relation.ispartofissue3en_US
dc.relation.ispartofjournalAngewandte Chemieen_US
dc.relation.ispartofvolume119en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchOrganic Chemical Synthesisen_US
dc.subject.fieldofresearchcode030503en_US
dc.titleDisaccharides as Sialic Acid Aldolase Substrates: Synthesis of Disaccharides Containing a Sialic Acid at the Reducing Enden_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2007
gro.hasfulltextNo Full Text


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