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Silver-assisted gold-catalyzed solid phase synthesis of linear and branched oligosaccharides

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dc.contributor.author SUTAR, YOGESH en_US
dc.contributor.author VANGALA, MADHURI en_US
dc.contributor.author HOTHA, SRINIVAS en_US
dc.date.accessioned 2021-12-24T11:37:49Z
dc.date.available 2021-12-24T11:37:49Z
dc.date.issued 2022-01 en_US
dc.identifier.citation Chemical Communications, 58,(5) 641-644. en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.issn 1364-548X en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6490
dc.identifier.uri https://doi.org/10.1039/D1CC06270K en_US
dc.description.abstract Unlike 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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.subject 2021-DEC-WEEK3 en_US
dc.subject TOC-DEC-2021 en_US
dc.subject 2022 en_US
dc.title Silver-assisted gold-catalyzed solid phase synthesis of linear and branched oligosaccharides en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Communications en_US
dc.publication.originofpublisher Foreign en_US


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