152174-28-2Relevant academic research and scientific papers
Selective acetolysis of 6-deoxy-sugar oligosaccharide building blocks governed by the armed-disarmed effect
Bedini, Emiliano,Comegna, Daniela,Nola, Annalida Di,Parrilli, Michelangelo
, p. 2546 - 2551 (2008/09/21)
The effect of the arming-disarming protection in the acetolysis of 6-deoxy-sugar oligosaccharides has been for the first time systematically investigated. Starting from the newly synthesized methyl glycosides, the acetolysis conditions employed here afforded 1-O-Ac oligosaccharides selectively without cleavage of the interglycosidic bonds, if a suitable protecting group pattern was used. Actually, the behavior of armed-disarmed, armed-armed, and disarmed-disarmed 6-deoxy-sugar disaccharides in acetolysis reactions was investigated: the results fit well with the prediction made on the basis of the armed-disarmed effect.
Synthesis of O-α-D-Rhap-(1 → 3)-O-α-D-Rhap-(1 → 2)-O-α-D-Rhap-(1 → 12)-oxydodecanoyl-bovine serum albumin
Zou,Sen,Szarek,MacLean
, p. 2194 - 2200 (2007/10/02)
The title compound (19), a conjugate of a trisaccharide based upon the repeating trisaccharide of α-D-rhamnose, which comprises the polysaccharide portion of 'A-band' lipopolysaccharide from a mutant (AK1401) of Pseudomonas aeruginosa, strain PAO1, with b
