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A new and novel approach towards the synthesis of 3'-deoxy-3'-hydroxymethyl ribofuosides
dc.contributor.authorPudlo, Jeffrey S.en_US
dc.contributor.authorTownsend, Leroy B.en_US
dc.date.accessioned2006-04-10T13:59:39Z
dc.date.available2006-04-10T13:59:39Z
dc.date.issued1990en_US
dc.identifier.citationPudlo, Jeffrey S., Townsend,, Leroy B. (1990)."A new and novel approach towards the synthesis of 3'-deoxy-3'-hydroxymethyl ribofuosides." Tetrahedron Letters 31(22): 3101-3104. <http://hdl.handle.net/2027.42/28964>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42H2FHM-2HH/2/7eea934dfa4a82ea64d78a89e0a469b6en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28964
dc.description.abstractThe synthesis of 1,2,5 tri--benzoyl-3-deoxy-3-[(benzyloxy)methyl]-[alpha],gb-D-ribofuranose () from 1,2 --isopropylidene-[alpha]-D-xylofuranose () has been achieved in an overall yield of 37%. Compound is a properly substituted intermediate for the synthesis of novel 3'-"branched" nucleoside analogs.en_US
dc.format.extent212493 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA new and novel approach towards the synthesis of 3'-deoxy-3'-hydroxymethyl ribofuosidesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_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 Chemistry, College of Literature, Science, and Arts and Department of Medicinal Chemistry, College of Pharmacy University of Michigan, Ann Arbor, Michigan, 48109 U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, College of Literature, Science, and Arts and Department of Medicinal Chemistry, College of Pharmacy University of Michigan, Ann Arbor, Michigan, 48109 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28964/1/0000801.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)94705-1en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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