Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6490
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dc.contributor.authorSUTAR, YOGESHen_US
dc.contributor.authorVANGALA, MADHURIen_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2021-12-24T11:37:49Z
dc.date.available2021-12-24T11:37:49Z
dc.date.issued2022-01en_US
dc.identifier.citationChemical Communications, 58,(5) 641-644.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6490
dc.identifier.urihttps://doi.org/10.1039/D1CC06270Ken_US
dc.description.abstractUnlike solid phase synthesis of peptides, synthesis of oligosaccharides by solid phase methods is lagging behind owing to inherent challenges faced while executing glycosidations. In this communication, silver-assisted gold-catalyzed glycosidations are found to be excellent for solid phase oligosaccharide synthesis. Glycosidations under catalytic conditions, one time coupling with four equivalents of donor, reactions in less than 30 min at 25 °C and on-resin deprotection of silyl and benzoate protecting groups are the salient features. Photocleaved glycans possess a protected amino functionality that can be utilized for bioconjugation. The versatility of this approach is established by synthesizing linear and branched pentaarabinofuranosides.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2021-DEC-WEEK3en_US
dc.subjectTOC-DEC-2021en_US
dc.subject2022en_US
dc.titleSilver-assisted gold-catalyzed solid phase synthesis of linear and branched oligosaccharidesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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