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dc.contributor.authorChao, Chin-Shengen_US
dc.contributor.authorChen, Min-Chunen_US
dc.contributor.authorLin, Shih-Cheen_US
dc.contributor.authorMong, Kwok-Kong T.en_US
dc.date.accessioned2014-12-08T15:12:19Z-
dc.date.available2014-12-08T15:12:19Z-
dc.date.issued2008-04-07en_US
dc.identifier.issn0008-6215en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.carres.2008.01.014en_US
dc.identifier.urihttp://hdl.handle.net/11536/9469-
dc.description.abstractInexpensive and readily available sulfonic acids, p-toluenesulfonic acid, and sulfuric acid are versatile and efficient catalysts for the peracetylation of a broad spectrum of carbohydrate substrates in good yield and in a practical time frame. Three appealing features in sulfonic acid-catalyzed acetylation of free sugars were explored including (1) suppression of furanosyl acetate formation for D-galactose and L-fucose; (2) high yielding chemoselective acetylation of sialic acid under appropriate conditions; and (3) peracetylation of amino sugars with different amino protecting functions. Simple one-pot two step acetylation-thioglycosidation methods for the expeditious synthesis of p-tolyl per-O-acetyl thioglycosides were also delineated. (C) 2008 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectp-toluenesulfonic aciden_US
dc.subjectacid-catalyzed acetylationen_US
dc.subjectamino sugarsen_US
dc.subjectone-pot protecting group manipulationen_US
dc.titleVersatile acetylation of carbohydrate substrates with bench-top sulfonic acids and application to one-pot syntheses of peracetylated thioglycosidesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.carres.2008.01.014en_US
dc.identifier.journalCARBOHYDRATE RESEARCHen_US
dc.citation.volume343en_US
dc.citation.issue5en_US
dc.citation.spage957en_US
dc.citation.epage964en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000254692800016-
dc.citation.woscount14-
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