Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3614
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dc.contributor.authorKAYASTHA, ABHIJEET K.en_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-07-23T11:08:16Z
dc.date.available2019-07-23T11:08:16Z
dc.date.issued2012-05en_US
dc.identifier.citationChemical Communications, 48(57), 7161-7163.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3614-
dc.identifier.urihttps://doi.org/10.1039/C2CC32649Cen_US
dc.description.abstractGlycosidation with stable alkyl glycosyl donors using a catalytic amount of gold salts is promising. Herein, 1-ethynylcyclohexanyl glycosides are identified as novel donors at room temperature and mechanistic investigation showed that the leaving group simply extrudes out.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2012en_US
dc.titleVersatile gold catalyzed transglycosidation at ambient temperatureen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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