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