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dc.contributor.authorA. Karst, Nathalie
dc.contributor.authorF. Islam, Tasneem
dc.contributor.authorY. Avci, Fikri
dc.contributor.authorJ. Linhardt, Robert
dc.date.accessioned2017-05-03T15:05:19Z
dc.date.available2017-05-03T15:05:19Z
dc.date.issued2004
dc.date.modified2009-12-17T22:31:09Z
dc.identifier.issn00404039
dc.identifier.doi10.1016/j.tetlet.2004.06.131
dc.identifier.urihttp://hdl.handle.net/10072/27697
dc.description.abstractA variety of sulfo-protected monosaccharide donors and acceptors were investigated in glycosylation reactions. Trifluoroethylsulfonate (SO3TFE) group was compatible with a wide range of activation conditions commonly used with fluoride, imidate, and sulfide donors. In addition, the influence of a SO3TFE group, at the critical 2-position in glycosyl donor, on the stereoselectivity of the glycosylation reaction was studied.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherPergamon
dc.publisher.placeUnited Kingdom
dc.publisher.urihttp://www.elsevier.com/locate/tetlet
dc.relation.ispartofpagefrom6433
dc.relation.ispartofpageto6437
dc.relation.ispartofissue34
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume45
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleTrifluoroethylsulfonate protected monosaccharides in glycosylation reactions
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.date.issued2004
gro.hasfulltextNo Full Text
gro.griffith.authorIslam, Tasneem


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