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Non-Glycosidically Linked Pseudodisaccharides: Thioethers, Sulfoxides, Sulfones, Ethers, Selenoethers, and Their Binding to Lectins
dc.contributor.authorCumpstey, Ianen_US
dc.contributor.authorRamstadius, Clintonen_US
dc.contributor.authorAkhtar, Tashfeenen_US
dc.contributor.authorGoldstein, Irwin J.en_US
dc.contributor.authorWinter, Harry C.en_US
dc.date.accessioned2010-04-14T20:01:57Z
dc.date.available2011-03-01T16:26:42Zen_US
dc.date.issued2010-04en_US
dc.identifier.citationCumpstey, Ian; Ramstadius, Clinton; Akhtar, Tashfeen; Goldstein, Irwin J.; Winter, Harry C. (2010). "Non-Glycosidically Linked Pseudodisaccharides: Thioethers, Sulfoxides, Sulfones, Ethers, Selenoethers, and Their Binding to Lectins." European Journal of Organic Chemistry 2010(10): 1951-1970. <http://hdl.handle.net/2027.42/69166>en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.issn1099-0690en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/69166
dc.description.abstractHydrolytically stable non-glycosidically linked tail-to-tail pseudodisaccharides are linked by a single bridging atom remote from the anomeric centre of the constituent monosaccharides. Some such pseudodisaccharides with sulfur or oxygen bridges were found to act as disaccharide mimetics in their binding to the Banana Lectin and to Concanavalin A. A versatile synthetic route to a small library of such compounds is described.en_US
dc.format.extent531305 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWILEY-VCH Verlagen_US
dc.subject.otherChemistryen_US
dc.subject.otherGeneral Chemistryen_US
dc.titleNon-Glycosidically Linked Pseudodisaccharides: Thioethers, Sulfoxides, Sulfones, Ethers, Selenoethers, and Their Binding to Lectinsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory, 10691 Stockholm, Sweden, Fax: +46-8-15-4908en_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI 48109-5606, USAen_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI 48109-5606, USAen_US
dc.contributor.affiliationotherDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory, 10691 Stockholm, Sweden, Fax: +46-8-15-4908en_US
dc.contributor.affiliationotherDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory, 10691 Stockholm, Sweden, Fax: +46-8-15-4908en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/69166/1/1951_ftp.pdf
dc.identifier.doi10.1002/ejoc.200901481en_US
dc.identifier.sourceEuropean Journal of Organic Chemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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