Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2157
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dc.contributor.authorRao, Boddu Venkateswaraen_US
dc.contributor.authorManmode, Sujiten_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-03-15T11:23:08Z-
dc.date.available2019-03-15T11:23:08Z-
dc.date.issued2015-11en_US
dc.identifier.citationCarbohydrate Research, 417, 103-108.en_US
dc.identifier.issn1873-426Xen_US
dc.identifier.issn0008-6215en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2157-
dc.identifier.urihttps://doi.org/10.1016/j.carres.2015.09.009en_US
dc.description.abstractVarious thiosaccharides and 1-thiotrehaloses were synthesized exploiting salient features of gold-catalyzed glycosidation repertoire using alkynyl 1,2-orthoesters as glycosyl donors. The reaction was found to be general, high yielding, diastereoselective, fast, mild and catalytic.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectThioglycosidesen_US
dc.subject1-Thiotrehalosesen_US
dc.subjectGold catalysisen_US
dc.subjectOrthoestersen_US
dc.subjectGlycosidationen_US
dc.subject2015en_US
dc.titlePropargyl 1,2-orthoesters for stereoselective synthesis of thioglycosides and 1-thiotrehalosesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleCarbohydrate Researchen_US
dc.publication.originofpublisherForeignen_US
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