O-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ring

scientific article published on 6 March 2007

O-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ring is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1021/JO062431R
P8608Fatcat IDrelease_lwu2xenugjezjkdjjkodflkcsm
P932PMC publication ID2615472
P698PubMed publication ID17338570
P5875ResearchGate publication ID6467345

P50authorDavid CrichQ74971587
P2093author name stringWenju Li
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Factors affecting stereocontrol during glycosidation of 2,3-oxazolidinone-protected 1-tolylthio-N-acetyl-D-glucosamineQ46474104
Stereocontrolled formation of beta-glucosides and related linkages in the absence of neighboring group participation: influence of a trans-fused 2,3-O-carbonate groupQ46668931
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Ethyl 2-acetamido-4,6-di-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-d-glycopyranoside as a versatile GlcNAc donorQ62056622
Synthesis ofl-Daunosamine andl-Ristosamine Glycosides via Photoinduced Aziridination. Conversion to Thioglycosides for Use in Glycosylation ReactionsQ62761923
Oxazolidinone Protection of N-Acetylglucosamine Confers High Reactivity on the 4-Hydroxy Group in GlycosylationQ73252298
A new C(1)-auxiliary for anomeric stereocontrol in the synthesis of alpha-sialyl glycosidesQ74018376
The Thioglycoside and Glycosyl Phosphite of 5-Azido Sialic Acid: Excellent Donors for the alpha-Glycosylation of Primary Hydroxy Groups This research was supported by Academia Sinica (Taipei) and the NIH (USA)Q74357200
Stereoselective alpha-Sialylation with Sialyl Xanthate and Phenylsulfenyl Triflate as a PromotorQ74822576
Efficient Sialylation with Phenyltrifluoroacetimidates as Leaving GroupsQ79136609
N-benzyl-2,3-oxazolidinone as a glycosyl donor for selective alpha-glycosylation and one-pot oligosaccharide synthesis involving 1,2-cis-glycosylationQ80117208
Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and InhibitorsQ88519588
P433issue7
P407language of work or nameEnglishQ1860
P304page(s)2387-2391
P577publication date2007-03-06
P1433published inJournal of Organic ChemistryQ898967
P1476titleO-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ring
P478volume72

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