144240-36-8Relevant articles and documents
Approaches to intramolecular sialylation 2. * Synthesis of per-O-acetylated thioglycosides of N-acetylneuraminic acid containing an unprotected carboxy group
Kononov,Shpirt,Ito,Ogawa
, p. 1442 - 1446 (2003)
Various approaches to the synthesis of per-O-acetylated thioglycosides of N-acetylneuraminic acid (Neu5Ac) containing an unprotected carboxy group starting from the corresponding methyl esters were comparatively studied. One-step demethylation of methyl t
Synthesis of sialic acid derivatives as ligands for the myelin-associated glycoprotein (MAG)
Shelke, Sachin V.,Gao, Gan-Pan,Mesch, Stefanie,Gaethje, Heiko,Kelm, Soerge,Schwardt, Oliver,Ernst, Beat
, p. 4951 - 4965 (2008/03/14)
The trisaccharide substructure 13 of the ganglioside GQ1bα shows a remarkable affinity for the myelin-associated glycoprotein (MAG). In the search for structurally simplified and pharmacokinetically improved mimics of 13, sialosides with modifications at
A facile, large-scale preparation of the methyl 2-thioglycoside of N-acetylneuraminic acid, and its usefulness for the α-stereoselective synthesis of sialoglycosides
Hasegawa, Akira,Ohki, Hitoshi,Nagahama, Takao,Ishida, Hideharu,Kiso, Makoto
, p. 277 - 281 (2007/10/02)
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