185797-99-3Relevant academic research and scientific papers
A convenient synthesis of the core trisaccharide of the N-glycans
Lu, Zhichao,Ding, Ning,Zhang, Wei,Wang, Peng,Li, Yingxia
scheme or table, p. 3320 - 3323 (2011/07/08)
A convenient synthesis of the core trisaccharide of the N-glycans was described. Orthogonal one-pot glycosylation of three monosaccharide building blocks was performed to furnish β-glucosyl chitobiose, which was then transformed to β-mannosyl chitobiose b
Convenient synthesis of an N-glycan octasaccharide of the bisecting type
Wang, Guangfa,Zhang, Wei,Lu, Zhichao,Wang, Peng,Zhang, Xiuli,Li, Yingxia
experimental part, p. 2508 - 2515 (2009/07/25)
Convenient synthesis of an N-glycan octasaccharide (A) of the bisecting type was described. The stable and easily prepared orthoester F, 3 -O-chloroacetyl-4 ,6 -O-benzylidene-α-D-glucopyranose 1, 2 (chloromethyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-g
Chemoselective ligation applied to the synthesis of a biantennary N-linked glycoform of CD52
Pratt, Matthew R.,Bertozzi, Carolyn R.
, p. 6149 - 6159 (2007/10/03)
We report here a strategy for the synthesis of N-linked glycopeptide analogues that replace the glycosidic linkages extending from the core pentasaccharide with thioethers amenable to construction by chemoselective ligation. The key building block, a pent
A new strategy for the synthesis of the core trisaccharide of asparagine-linked sugar chains
Matsuo, Ichiro,Isomura, Megumi,Walton, Richard,Ajisaka, Katsumi
, p. 8795 - 8798 (2007/10/03)
The core trisaccharide common to all asparagine-linked glycoprotein olisosaccharides was synthesized using two novel processes: 1) regioselective acetylation using lipase, and 2) inversion of the C-2 hydroxyl group of the glucose residue in a glucosyl chi
