Abstract
A methodology allowing the differentiation of azido groups in protected oligosaccharides was optimized. It allowed the first synthesis of tetrasaccharides 1 and 2 containing both N-acetylated and N-unsubstituted glucosamine, as well as glucuronic and/or iduronic acid residues. These tetrasaccharides were then examined for their ability to interact with 10E4, an antibody recognizing early lesions in the brain of scrapie prion-infected mice.
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