132360-46-4Relevant academic research and scientific papers
Synthesis of oligosaccharide fragments of mannan from Candida albicans cell wall and their BSA conjugates
Karelin,Tsvetkov,Kogan,Bystricky,Nifantiev
, p. 110 - 121 (2008/03/13)
3-Aminopropyl glycosides of α-D-mannopyranosyl-(1→2)-α-D- mannopyranosyl-(1→2)-α-D-mannopyranosyl-(1→2) -α-D-mannopyranose, α-D-mannopyranosyl-(1→3)-α-D- mannopyranosyl-(1→2)-α-D-mannopyranosyl-(1→2) -α-D-mannopyranose, and α-D-mannopyranosyl-(1→2)-[α-D- mannopyranosyl-(1→3)]-α-D-mannopyranosyl-(1→2) -α-D-mannopyranosyl-(1→2)-α-D-mannopyranose were efficiently synthesized starting from ethyl 2-O-acetyl(benzoyl)-3,4,6-tri-O-benzyl-1-thio- α-D-mannopyranoside, ethyl 4,6-di-O-benzyl-2-O-benzoyl-1-thio-α-D- mannopyranoside, ethyl 4,6-di-O-benzyl-2,3-di-O-benzoyl-1-thio-α-D- mannopyranoside, and 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl bromide. The oligosaccharide chains synthesized correspond to the three structural types of side chains of mannan from Candida albicans cell wall. A conjugate of the third pentasaccharide with bovine serum albumin was prepared using the squarate method.
Glycosylation using a one-electron-transfer, homogeneous reagent. Application to an efficient synthesis of the trimannosyl core of N-glycosylproteins
Zhang, Yong-Min,Mallet, Jean-Maurice,Sinay, Pierre
, p. 73 - 88 (2007/10/02)
Double glycosylation of methyl 2,4-di-O-benzyl-β-D-mannopyranoside with ethyl 2-O-benzoyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside using as promoter tris(4-bromophenyl)ammoniumyl hexachloroantimonate, a stable, commercial, and crystalline radical cat
