Regioselective sulfation of galactose derivatives through the stannylene procedure. New synthesis of the 3′-O-sulfated Lewisa trisaccharide

Tetrahedron Letters

Volumn 35, Issue 47, 1994, Pages 8795-8796

  Lubineau, André ^a   Lemoine, Rémy ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARBOHYDRATE SYNTHESIS; REACTION ANALYSIS; SULFATION;

EID: 0028007115     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78500-5     Document Type: Article

References (13)

1. Proteoglycans: Structures and Interactions
2. Proteoglycans in health and disease: structures and functions.
3. Sulfated blood group Lewis(a). A superior oligosaccharide ligand for human E-selectin.
4. High affinity binding of the leucocyte adhesion molecule L-selectin to 3′-sulphated-Lea and -Lex oligosaccharides and the predominance of sulphate in this interaction demonstrated by binding studies with a series of lipid-linked oligosaccharides
5. Adv. Carbohydr. Chem.
6. Regioselective manipulation of hydroxyl groups via organotin derivatives
7. First synthesis of the 3?-sulfated Lewis trisaccharide, putative ligand for the leucocyte homing receptor
8. Selectivity in the catalytic transfer hydrogenolysis of silyl ether protecting groups