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dc.contributor.authorPradhan, Tapan Kumaren_US
dc.contributor.authorLin, Chun Chengen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2014-12-08T15:35:26Z-
dc.date.available2014-12-08T15:35:26Z-
dc.date.issued2014-03-07en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol500275jen_US
dc.identifier.urihttp://hdl.handle.net/11536/23988-
dc.description.abstractA practical method for the synthesis of KDO glycal donors was developed. The prepared KDO donors exhibited excellent disastereoselectivity of glycosylation in a CH2Cl2-CH3CN solvent mixture, which was found to be associated with the isopropylidene protection at the C-4 and C-5 hydroxyls. The synthetic use of the KDO donor was demonstrated in the preparation of beta-KDO-containing oligosaccharides.en_US
dc.language.isoen_USen_US
dc.titlePreparation of a Protected 3-Deoxy-D-manno-oct-2-ulosonate Glycal Donor for the Synthesis of beta-KDO-Containing Oligosaccharidesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol500275jen_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume16en_US
dc.citation.issue5en_US
dc.citation.spage1474en_US
dc.citation.epage1477en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000332756400051-
dc.citation.woscount2-
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