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dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.contributor.authorYen, Yu-Fangen_US
dc.contributor.authorHung, Wei-Chengen_US
dc.contributor.authorLai, Yen-Hsunen_US
dc.contributor.authorChen, Jiun-Hanen_US
dc.date.accessioned2014-12-08T15:23:16Z-
dc.date.available2014-12-08T15:23:16Z-
dc.date.issued2012-05-01en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/16334-
dc.description.abstractMost natural 2-acetamido-2-deoxyglycosides exist in a 1,2-trans-beta-glycosidic configuration. This study investigated the use of 2-azido-2-deoxythioglycosides for 1,2-trans-beta-glycosidic bond formation under low-concentration glycosylation conditions. Further application of the 2-azido-2-deoxythioglycosyl substrates for one-pot oligosaccharide synthesis was demonstrated in the synthesis of protected beta-(1?6)-N-acetylglucosamine trimer, core-6serine conjugate, and F1a serine conjugate.en_US
dc.language.isoen_USen_US
dc.subjectAzidesen_US
dc.subjectCarbohydratesen_US
dc.subjectGlycosylationen_US
dc.subjectGlycopeptidesen_US
dc.subjectRegioselectivityen_US
dc.titleApplication of 2-Azido-2-deoxythioglycosides for beta-Glycoside Formation and Oligosaccharide Synthesisen_US
dc.typeArticleen_US
dc.identifier.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volumeen_US
dc.citation.issue15en_US
dc.citation.epage3009en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000303994100014-
dc.citation.woscount6-
Appears in Collections:Articles


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