Title of article :
2,6-Anhydroaldonic acids; Methyl 2,6-anhydroaldonates; 2,6-Anhydroaldonamides; Anhydroalditols; Anhydrodeoxynitroalditols
Author/Authors :
Ennio Bousquet، نويسنده , , Malika Khitri، نويسنده , , Luigi Lay، نويسنده , , Francesco Nicotra، نويسنده , , Luigi Panza، نويسنده , , Giovanni Russo، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 1998
Pages :
11
From page :
171
To page :
181
Abstract :
A new and more versatile synthesis of β-d-ManpNAc-(1→4)-α-d-Glcp-(1→2)-α-l-Rhap, the trisaccharide repeating unit of the Streptococcus pneumoniae type 19F capsular polysaccharide, is described. The present approach allows a simple access to different fragments containing the trisaccharide and the conjugation of the product(s) to a protein through the selective manipulation of the anomeric position at the reducing end and of the HO-4 function at the nonreducing end. The synthetic scheme shows an efficient application of the sulfoxide method for the stereoselective and high yielding formation of the glycosidic linkages.
Keywords :
Glycoconjugate vaccines , Streptococcus pneumoniae , Oligosaccharides , synthesis , Glycosylation , Anomeric sulfoxides
Journal title :
Carbohydrate Research
Serial Year :
1998
Journal title :
Carbohydrate Research
Record number :
962550
Link To Document :
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