dc.contributor.author | A. Karst, Nathalie | |
dc.contributor.author | F. Islam, Tasneem | |
dc.contributor.author | Y. Avci, Fikri | |
dc.contributor.author | J. Linhardt, Robert | |
dc.date.accessioned | 2017-05-03T15:05:19Z | |
dc.date.available | 2017-05-03T15:05:19Z | |
dc.date.issued | 2004 | |
dc.date.modified | 2009-12-17T22:31:09Z | |
dc.identifier.issn | 00404039 | |
dc.identifier.doi | 10.1016/j.tetlet.2004.06.131 | |
dc.identifier.uri | http://hdl.handle.net/10072/27697 | |
dc.description.abstract | A 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.peerreviewed | Yes | |
dc.description.publicationstatus | Yes | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | Pergamon | |
dc.publisher.place | United Kingdom | |
dc.publisher.uri | http://www.elsevier.com/locate/tetlet | |
dc.relation.ispartofpagefrom | 6433 | |
dc.relation.ispartofpageto | 6437 | |
dc.relation.ispartofissue | 34 | |
dc.relation.ispartofjournal | Tetrahedron Letters | |
dc.relation.ispartofvolume | 45 | |
dc.subject.fieldofresearch | Medicinal and Biomolecular Chemistry | |
dc.subject.fieldofresearch | Organic Chemistry | |
dc.subject.fieldofresearchcode | 0304 | |
dc.subject.fieldofresearchcode | 0305 | |
dc.title | Trifluoroethylsulfonate protected monosaccharides in glycosylation reactions | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dc.type.code | C - Journal Articles | |
gro.date.issued | 2004 | |
gro.hasfulltext | No Full Text | |
gro.griffith.author | Islam, Tasneem | |