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Synthesis of p-nitrophenyl 2-O-[alpha]--mannopyranosyl-[alpha]--mannopyranoside and p-nitrophenyl 6-O-[alpha]--mannopyranosyl-[alpha]--mannopyranoside

dc.contributor.authorReichert, Cheryl M.en_US
dc.date.accessioned2006-04-07T17:31:08Z
dc.date.available2006-04-07T17:31:08Z
dc.date.issued1979-12en_US
dc.identifier.citationReichert, Cheryl M. (1979/12)."Synthesis of p-nitrophenyl 2-O-[alpha]--mannopyranosyl-[alpha]--mannopyranoside and p-nitrophenyl 6-O-[alpha]--mannopyranosyl-[alpha]--mannopyranoside." Carbohydrate Research 77(1): 141-147. <http://hdl.handle.net/2027.42/23445>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TFF-42H94D1-185/2/030c993706e0103d8544e5a009b772d9en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23445
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=519654&dopt=citationen_US
dc.description.abstractCrystalline 2-O-[alpha]--mannopyranosyl-[beta]--mannopyranose octaacetate was synthesized by condensation of tetra-O-acetyl-[alpha]--mannopyranosyl bromide (3) with 1,3,4,6-tetra-O-acetyl-[beta]--mannopyranose. 6-O-[alpha]--mannopyranosyl-[alpha]--mannopyranose octaacetate was prepared by condensation of 3 with 1,2,3,4-tetra-O-acetyl-6-O-trityl-[alpha]--mannopyranose. Fusion of each mannobiosyl octaacetate with p-nitrophenol was followed by deacetylation, to give the corresponding p-nitrophenyl (1--&gt;2)- and (1--&gt;6)-[alpha]--mannobioside.en_US
dc.format.extent966223 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleSynthesis of p-nitrophenyl 2-O-[alpha]--mannopyranosyl-[alpha]--mannopyranoside and p-nitrophenyl 6-O-[alpha]--mannopyranosyl-[alpha]--mannopyranosideen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48104 U.S.A.en_US
dc.identifier.pmid519654en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23445/1/0000395.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0008-6215(00)83800-8en_US
dc.identifier.sourceCarbohydrate Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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