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A straightforward alpha-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl alpha-T-antigen

dc.citation.epage438en_US
dc.citation.issue4en_US
dc.citation.spage432en_US
dc.citation.volume344en_US
dc.citation.woscount6
dc.contributor.authorChang, Shih-Shengen_US
dc.contributor.authorLin, Chun-Chengen_US
dc.contributor.authorLi, Yaw-Kuenen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:09:47Z
dc.date.available2014-12-08T15:09:47Z
dc.date.issued2009-03-10en_US
dc.description.abstractA practical and efficient alpha-selective aromatic glycosylation with simple per-O-acetyl glycopyranosyl trichloroacetimidates is reported. The method is particularly effective for L-fucosyl and 2-azido-2-deoxy-D-galatosaminyl imidates, with which exclusive alpha-selectivity was achieved. The synthetic utility of this method was demonstrated in the stereoselective synthesis of 4-methylumbelliferyl alpha-T-antigen. (C) 2008 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.carres.2008.12.013en_US
dc.identifier.issn0008-6215en_US
dc.identifier.journalCARBOHYDRATE RESEARCHen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.carres.2008.12.013en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/7494
dc.identifier.wosnumberWOS:000264615900003
dc.language.isoen_USen_US
dc.subjectStereoselectiveen_US
dc.subjectAromaticen_US
dc.subjectGlycosylationen_US
dc.subjectImidateen_US
dc.subjectalpha-T-Antigenen_US
dc.titleA straightforward alpha-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl alpha-T-antigenen_US
dc.typeArticleen_US

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