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Without protecting groups, polymer-bound thioglycosyl sugars can undergo two successive glycosylation reactions, once as a donor and once as an acceptor, to give trisaccharides such as 1. Trisaccharide libraries prepared by this strategy have a known sugar residue at the reducing or nonreducing ends. •=polymer resin+amide linker.
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Zhu et al. (1998) studied this question.
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