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dc.contributor.authorNokami, Toshikien_US
dc.contributor.authorHayashi, Ryutaroen_US
dc.contributor.authorSaigusa, Yoshihiroen_US
dc.contributor.authorShimizu, Akihiroen_US
dc.contributor.authorLiu, Chih-Yuehen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.contributor.authorYoshida, Jun-ichien_US
dc.date.accessioned2014-12-08T15:34:16Z-
dc.date.available2014-12-08T15:34:16Z-
dc.date.issued2013-09-06en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol402034gen_US
dc.identifier.urihttp://hdl.handle.net/11536/23482-
dc.description.abstractA new iterative one-pot sequential method for the solution-phase synthesis of oligosaccharides has been devised on the basis of the electrochemical oxidation of a propagating thioglycoside terminus to generate the corresponding triflate, followed by the reaction with a thioglycoside building block having a free hydroxyl group. A practical automated synthesizer was developed for the method and was effectively used for assembling up to six thioglycoside building blocks to synthesize partial structures of poly-beta-D-(1-6)-N-acetylglucosamine.en_US
dc.language.isoen_USen_US
dc.titleAutomated Solution-Phase Synthesis of Oligosaccharides via Iterative Electrochemical Assembly of Thioglycosidesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol402034gen_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume15en_US
dc.citation.issue17en_US
dc.citation.spage4520en_US
dc.citation.epage4523en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000328864800063-
dc.citation.woscount6-
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