A general synthesis of model glycoproteins: coupling of alkenyl glycosides to proteins, using reductive ozonolysis followed by reductive amination with sodium cyanoborohydride

Carbohydrate Research

Volumn 78, Issue 1, 1980, Pages

  Bernstein, Michael A ^a   Hall, Laurance D ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0002218582     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6215(00)83676-9     Document Type: Article

References (31)

1. Synthesis of 3-O-[6-O-(?-D-galactopyranosyl)-?-D-galactopyranosyl]-1,2-di-O-stearoyl-L-glycerol, a ?digalactosyl diglyceride?
2. Synthesis of a new class of model glycolipids
3. The allyl ether as a protecting group in carbohydrate chemistry. Part VII. The 2-O-allyl group as a non-participant in 1,2-cis-glycoside synthesis
4. The Oxidation of Acetals by Ozone
5. Deuterium nuclear magnetic resonance measurements of glycoproteins which have been specifically deuterated either at selected carbohydrate or at lysine residues: determination of motional correlation times