2024-03-29T10:17:37Zhttps://eprints.lib.hokudai.ac.jp/dspace-oai/requestoai:eprints.lib.hokudai.ac.jp:2115/475542022-11-17T02:08:08Zhdl_2115_20055hdl_2115_8527A potential glucuronate glycosyl donor with 2-O-acyl-6,3-lactone structure: efficient synthesis of glycosaminoglycan disaccharidesFurukawa, TakayukiHinou, HiroshiShimawaki, KenNishimura, Shin-IchiroGlycosylationLactonesCarbohydrateGlycosaminoglycans1,2-trans Stereoselectivity464Development of β-selective glucuronylation reaction using phenyl 2,4-di-O-acetyl-1-thio-β-D-glucopyranosidurono-6,3-lactone was described. Glycosylations of this glycosyl donor with hexosamine derivatives proceeded with excellent yield and β-stereoselectivity to afford glycosaminoglycan-type disaccharides.ElsevierJournal Articleapplication/pdfhttp://hdl.handle.net/2115/47554https://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/47554/1/TL52-43_5567-5570.pdf0040-4039Tetrahedron Letters5243556755702011-10-26enginfo:doi/10.1016/j.tetlet.2011.08.024author