Article ID Journal Published Year Pages File Type
5269091 Tetrahedron Letters 2011 4 Pages PDF
Abstract
Development 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.
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Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
A potential glucuronate glycosyl donor with 2-O-acyl-6,3-lactone structure: efficient synthesis of glycosaminoglycan disaccharides
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