Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4609
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dc.contributor.authorANAND, SAURABHen_US
dc.contributor.authorMARDHEKAR, SANDHYAen_US
dc.contributor.authorRAIGAWALI, RAKESHen_US
dc.contributor.authorMOHANTA, NIRMALAen_US
dc.contributor.authorJAIN, PRASHANTen_US
dc.contributor.authorSHANTHAMURTHY, CHETHAN D.en_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.contributor.authorKIKKERI, RAGHAVENDRAen_US
dc.date.accessioned2020-05-22T13:07:13Z
dc.date.available2020-05-22T13:07:13Z
dc.date.issued2020-04en_US
dc.identifier.citationOrganic Letters, 22(9), 3402-3406.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4609-
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.0c00878en_US
dc.description.abstractWe report for the first time a continuous-flow strategy to execute O-sulfation modification of heparan sulfate (HS) oligosaccharides. A systematic investigation of the influence of the flow parameters on the installation of the sulfate group on glucosamine monosaccharide can aid the development of a comprehensive, quick, and reliable strategy for O-sulfation of HS oligosaccharide precursors. Deprotection of the sulfated heparin intermediates led to the development of a comprehensive biologically inspired oligosaccharide library to understand the crucial structure–function relationship of HS.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectBindingen_US
dc.subjectOligosaccharidesen_US
dc.subjectActivationen_US
dc.subjectTOC-MAY-2020en_US
dc.subject2020en_US
dc.subject2020-MAY-WEEK3en_US
dc.titleContinuous-Flow Accelerated Sulfation of Heparan Sulfate Intermediatesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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