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pubmed-article:16910646pubmed:dateCreated2006-8-16lld:pubmed
pubmed-article:16910646pubmed:abstractTextGlycosylation reactions using N-benzyl-2,3-trans-oxazolidinones as the glycosyl donors were shown to be highly alpha-selective. Advantages of the donor include facile preparation in gram-scale preparation and simple deprotection procedures. Subsequently, a one-pot oligosaccharide synthesis involving 1,2-cis glycosidic linkages was demonstrated using the novel glycosyl donors.lld:pubmed
pubmed-article:16910646pubmed:languageenglld:pubmed
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pubmed-article:16910646pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:16910646pubmed:monthAuglld:pubmed
pubmed-article:16910646pubmed:issn0002-7863lld:pubmed
pubmed-article:16910646pubmed:authorpubmed-author:ManabeShinoSlld:pubmed
pubmed-article:16910646pubmed:authorpubmed-author:ItoYukishigeYlld:pubmed
pubmed-article:16910646pubmed:authorpubmed-author:IshiiKazuyuki...lld:pubmed
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pubmed-article:16910646pubmed:day23lld:pubmed
pubmed-article:16910646pubmed:volume128lld:pubmed
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pubmed-article:16910646pubmed:authorsCompleteYlld:pubmed
pubmed-article:16910646pubmed:pagination10666-7lld:pubmed
pubmed-article:16910646pubmed:dateRevised2008-1-17lld:pubmed
pubmed-article:16910646pubmed:year2006lld:pubmed
pubmed-article:16910646pubmed:articleTitleN-benzyl-2,3-oxazolidinone as a glycosyl donor for selective alpha-glycosylation and one-pot oligosaccharide synthesis involving 1,2-cis-glycosylation.lld:pubmed
pubmed-article:16910646pubmed:affiliationRIKEN, The Institute of Physical and Chemical Research, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan. smanabe@riken.jplld:pubmed
pubmed-article:16910646pubmed:publicationTypeJournal Articlelld:pubmed
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