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dc.contributor.authorvon Itzstein, Marken_US
dc.contributor.authorJ. Owen, Daviden_US
dc.date.accessioned2017-05-03T13:29:45Z
dc.date.available2017-05-03T13:29:45Z
dc.date.issued2000en_US
dc.identifier.issn00086215en_US
dc.identifier.doi10.1016/S0008-6215(00)00110-5en_US
dc.identifier.urihttp://hdl.handle.net/10072/2982
dc.description.abstractAn efficient new entry into N,N-dialkyl-S-glycosylsulfenamides is reported. The reaction of bis-activated alkyl halides in the presence of a secondary amine base with glycosylic S-acetyl derivatives (1-S-acetyl-1-thioaldoses or 2-S-acetyl-2-thioketoses) results in the formation of novel carbohydrate sulfenamides. These new carbohydrate-based sulfenamides may provide useful derivatives with biological activity, as well as provide reactive carbohydrate sulfenylating agents.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.language.isoen_US
dc.publisherPergamonen_US
dc.publisher.placeUKen_US
dc.relation.ispartofpagefrom287en_US
dc.relation.ispartofpageto292en_US
dc.relation.ispartofjournalCarbohydrate Researchen_US
dc.relation.ispartofvolume328en_US
dc.subject.fieldofresearchHISTORY AND ARCHAEOLOGYen_US
dc.subject.fieldofresearchcode210000en_US
dc.titleA one-pot synthesis of novel N,N-dialkyl-S-glycosylsulfenamidesen_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.date.issued2015-05-04T22:02:38Z
gro.hasfulltextNo Full Text


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