4.5 Article

Synthesis of mucin O-glycan core structures as their p-nitro- and p-aminophenyl glycosides

期刊

CARBOHYDRATE RESEARCH
卷 346, 期 12, 页码 1454-1466

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.carres.2011.03.036

关键词

Mucin O-glycan core structures; Oxazolidinone protected glycosyl donors; Oligosaccharide synthesis

资金

  1. Science Foundation Ireland [08/SRC/B1393]
  2. Science Foundation Ireland (SFI) [08/SRC/B1393] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

For the investigation of glycosidases, and for the construction of glycan arrays the p-nitrophenyl- and p-aminophenyl glycosides of mucin O-glycan core structures 1-7 and the 2,6-ST-antigen have been chemically synthesized using D-galactose as a precursor for GalNAc residues. GlcNAc residues have partly been introduced using a 4,6-di-O-benzoyl-2,3-N,O-oxazolidinone-protected donor, which allowed deprotection of the formed di- and tri-saccharides in one step using sodium methoxide. (C) 2011 Elsevier Ltd. All rights reserved.

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