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pubmed-article:15043147pubmed:dateCreated2004-3-26lld:pubmed
pubmed-article:15043147pubmed:abstractTextThe syntheses of a novel uridine diphosphate galactose (UDP-Gal) analog, (UDP-2,4,6-tri-O-acetyl-3-S-acetyl-3-thio-alpha-D-galactopyranose) (11) and the thiolpyridine protected (Uridine 5'-[3-S-(2-S-pyridyl)-3-thio-alpha-D-galactopyranosyl diphosphate) analog (12) are described. The reported synthesis relies on the novel use of thiolpyridine to generate 12 which is a suitably protected intermediate for generating a UDP-thioGal derivative by reduction prior to enzyme transfer via beta-1,4-galactosyltransferase.lld:pubmed
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pubmed-article:15043147pubmed:statusMEDLINElld:pubmed
pubmed-article:15043147pubmed:issn1525-7770lld:pubmed
pubmed-article:15043147pubmed:authorpubmed-author:RiceKevin GKGlld:pubmed
pubmed-article:15043147pubmed:authorpubmed-author:ElhalabiJorda...lld:pubmed
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pubmed-article:15043147pubmed:volume23lld:pubmed
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pubmed-article:15043147pubmed:pagination195-205lld:pubmed
pubmed-article:15043147pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:15043147pubmed:year2004lld:pubmed
pubmed-article:15043147pubmed:articleTitleSynthesis of uridine 5'-[2-S-pyridyl-3-thio-alpha-D-galactopyranosyl diphosphate]: precursor of UDP-thiogal sugar nucleotide donor substrate for beta-1,4-galactosyltransferase.lld:pubmed
pubmed-article:15043147pubmed:affiliationDepartment of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, USA.lld:pubmed
pubmed-article:15043147pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15043147pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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