290330-40-4Relevant academic research and scientific papers
Highly regioselective synthesis of a 3-O-sulfonated arabino Lewisa asparagine building block suitable for glycopeptide synthesis
Roesch, Alexander,Kunz, Horst
, p. 1597 - 1608 (2007/10/03)
Using the stannylene method, the trisaccharide 2-acetamido-3-O-[6-O-benzyl-β-d-galactopyranosyl]-4-O-[2,3,4-tri-O-benzyl-β-d-arabinopyranosyl]-6-O-benzyl-2-deoxy-β-d-glucopyranosyl azide was regioselectively sulfonated and, after reduction of the anomeric
A Sialyl-Lewis A-asparagine building block for glycopeptide-synthesis
Peilst?cker, Karen,Kunz, Horst
, p. 820 - 822 (2007/10/03)
Using the azido group as the anomeric protection a Sialyl Lewis A tetrasaccharide was synthesized from N-acetylglucosamine via the type1 lactosamine and Lewis A intermediates. After reduction of the azido group, coupling with Fmoc α-allyl aspartate and Pd
