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1. (Article ID: 3829)
 
Cai X, Zong G, Xu Y, Zhang J, Liang X, Wang D
Efficient synthesis of a 6-deoxytalose tetrasaccharide related to the antigenic O-polysaccharide produced by Aggregatibacter actinomycetemcomitans serotype c
Carbohydrate Research 345(9) (2010) 1230-1234
 

Concise synthesis of a 6-deoxy-α-L-talose tetrasaccharide, 6-deoxy-α-L-Talp-(1→3)-6-deoxy-α-L-Talp-(1→2)-6-deoxy-α-L-Talp-(1→3)-6-deoxy-α-L-Talp, the dimer of the disaccharide repeating unit of the OPS from Aggregatibacter actinomycetemcomitans serotype c, has been accomplished through suitable protecting group manipulations and stereoselective glycosylation starting from commercially available L-rhamnose. The target oligosaccharide in the form of its p-methoxyphenyl glycoside is suitable for further glycoconjugate formation via selective cleavage of this group.

tetrasaccharide, rhamnose, selective acylation, 6-deoxya-L-talose

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