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Tandem One-Pot Acetalation-Acetylation for Direct Access to Differentially Protected Thioglycosides and O-Glycosides with p-Toluenesulfonic Acid

dc.citation.epage606en_US
dc.citation.issue4en_US
dc.citation.spage603en_US
dc.citation.volumeen_US
dc.citation.woscount5
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.contributor.authorChao, Chin-Shengen_US
dc.contributor.authorChen, Min-Chunen_US
dc.contributor.authorLin, Chun-Weien_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.issued2009-03-03en_US
dc.description.abstractA new tandem one-pot acetalation-acetylation procedure is reported which streamlines routine protecting-group manipulation of carbohydrate molecules in production of differentially protected 0- and thioglycosides. This new procedure eliminates the use of highly toxic pyridine, and p-toluenesulfonic acid is employed as catalyst for acetalation and acetylation. Synthetic utility of the new procedure is demonstrated in the expeditious preparation of differentially protected glycosides from a wide variety of carbohydrate substrates including unprotected O-glycosides, thioglycosides, and N-acetyl neuraminic acid ester.en_US
dc.identifier.doi10.1055/s-0028-1087913en_US
dc.identifier.issn0936-5214en_US
dc.identifier.journalSYNLETTen_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0028-1087913en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/7506
dc.identifier.wosnumberWOS:000264658300016
dc.language.isoen_USen_US
dc.subjecttandemen_US
dc.subjectacetalsen_US
dc.subjectglycosidesen_US
dc.subjectoligosaccharidesen_US
dc.subjectprotecting groupen_US
dc.titleTandem One-Pot Acetalation-Acetylation for Direct Access to Differentially Protected Thioglycosides and O-Glycosides with p-Toluenesulfonic Aciden_US
dc.typeArticleen_US

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