640273-67-2Relevant academic research and scientific papers
Trifluoroethylsulfonate protected monosaccharides in glycosylation reactions
Karst, Nathalie A.,Islam, Tasneem F.,Avci, Fikri Y.,Linhardt, Robert J.
, p. 6433 - 6437 (2007/10/03)
A variety of sulfo-protected monosaccharide donors and acceptors were investigated in glycosylation reactions. Trifluoroethylsulfonate (SO 3TFE) group was compatible with a wide range of activation conditions commonly used with fluoride, imidat
Sulfo-Protected Hexosamine Monosaccharides: Potentially Versatile Building Blocks for Glycosaminoglycan Synthesis
Karst, Nathalie A.,Islam, Tasneem F.,Linhardt, Robert J.
, p. 4839 - 4842 (2007/10/03)
(Equation Presented) 2,2,2-Trifluorodiazoethane was investigated as a reagent for sulfo group protection on hexosamine monosaccharides. The synthesis of glucosamine and galactosamine building blocks fully differentiated for glycosaminoglycan synthesis and
