503159-47-5Relevant academic research and scientific papers
Synthesis of aminoethyl glycosides of the ganglioside GM1 and asialo-GM1 oligosaccharide chains
Cheshev,Khatuntseva,Tsvetkov,Shashkov,Nifantiev
, p. 60 - 70 (2007/10/03)
4′-O-Glycosylation of 2-azidoethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O- benzyl-6-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranoside with a disaccharide donor, 4-trichloroacetamidophenyl 4,6-di-O-acetyl-2-deoxy-3-O-(2,3, 4,6-tetra-O-acetyl-β-D-galactopyranos
Synthesis of a spacer-armed disulfated tetrasaccharide of SB1a, a carbohydrate hapten associated with human hepatocellular carcinoma
Li, Qin,Li, Hui,Li, Qing,Lou, Qing-Hua,Su, Bin,Cai, Meng-Shen,Li, Zhong-Jun
, p. 1929 - 1934 (2007/10/03)
A disulfated tetrasaccharide fragment with a spacer arm of human hepatocellular carcinoma carbohydrate antigen SB1a, namely, 2-aminoethyl 3-O-sulfo-β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D- galactopyranosyl-(1→4)-3-O-sulfo-β-D-galactopyranosyl-(1→4)- β-D-glucopyranoside was synthesized via a [2+1+1] block building mode. In the last coupling step toward the trisaccharide acceptor 8, benzoyl protected galactosyl bromide donor 14 was found to be much more reactive than the acetyl-protected donors.
