Huang, Bo-Shun; Lowary, Todd L. published the artcile< β-Selective xylulofuranosylation via a conformationally-restricted glycosyl donor>, Related Products of 4064-06-6, the main research area is xylulofuranosylation stereoselective glycosylation lipopolysaccharide antigen; crystal structure xylulofuranose lipopolysaccharide antigen Yersinia enterocolitica oligosaccharide.
Reported is the first stereoselective method for β-xylulofuranosylation, which employs 3,4-O-xylylene-protected thioglycoside donors. For most acceptors, the best results were observed with a donor that possesses both the xylylene group and a benzoate ester at O-1. To demonstrate its utility, the methodol. was applied to the first synthesis of the pentasaccharide repeating unit from the lipopolysaccharide O-antigen of Yersinia enterocolitica serovars, a structure containing two β-xylulofuranose residues.
Organic & Biomolecular Chemistry published new progress about Antigens Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 4064-06-6 belongs to class alcohols-buliding-blocks, and the molecular formula is C12H20O6, Related Products of 4064-06-6.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts