82916-19-6Relevant academic research and scientific papers
A highly α-stereoselective synthesis of oligosaccharide fragments of the VI antigen from salmonella typhi and their antigenic activities
Yang, Lin,Zhu, Jingjing,Zheng, Xiu-Jing,Tai, Guihua,Ye, Xin-Shan
, p. 14518 - 14526 (2012/02/14)
In this paper, a convenient approach to the synthesis of the repeating α-(1→4)-linked N-acetyl galactosaminuronic acid units from the capsular polysaccharide of Salmonella typhi is reported. The exclusively α-stereoselective glycosylation reactions were a
2-Substituted methyl alpha-D-galactopyranosides: synthesis and binding affinity for the A and B subunits of the Griffonia simplicifolia I isolectins.
Kaifu,Plantefaber,Goldstein
, p. 37 - 49 (2007/10/02)
The binding affinities of the N-acetyl, N-trifluoroacetyl, N-propionyl, N-formyl, N-benzoyl, N-p-nitrobenzoyl, N-p-aminobenzoyl, and N-methyl derivatives of methyl 2-amino-2-deoxy-alpha-D-galactopyranoside and the 2-O-acetyl, -benzoyl, -benzyl, and -methyl derivatives of methyl alpha-D-galactopyranoside for the A and B subunits of the Griffonia simplicifolia I isolectins have been determined by hapten inhibition analysis of a galactomannan-isolectin precipitation system. Models for these carbohydrate-protein interactions are presented together with an interpretation of the results on the basis of electronic and steric effects.
