Synthesis of Neoglycoproteins as Artificial Antigens

Abstract
The synthesis of various allyl glycosides of L-rhamnose containing ether and/or ester substituents are reported. Ozonolysis of allyl glycosides followed by reductive amination with ∊-amino groups of lysine residues in bovine serum albumin using sodium cyanoborohydride at pH 7.8 provided different structural neoglycoproteins as artificial antigens.

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