115945-97-6Relevant articles and documents
Synthesis of 4-nitrophenyl 2-acetamido-2-deoxy-β-D-mannopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-α-D-mannopyranoside
Krist, Pavel,Kuzma, Marek,Pelyvas, Istvan F.,Simerska, Pavla,Kren, Vladimir
, p. 801 - 811 (2007/10/03)
The title compounds were synthesized by the selective reduction of the azido group in 4-nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranoside (8) and 4-nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-β-D-mannopyranoside (11), and by subsequent acetylation. Compound 8 was prepared by opening of the epoxide ring in methyl 2,3-anhydro-4,6-O-benzylidene-α-D-glucopyranoside (1) with sodium azide, followed by inversion of the configuration at C-3 in the resulting altropyranoside and glycosidation with 4-nitrophenol.
SYNTHESIS OF A TRISACCHARIDE COMPONENT OF THE CAPSULAR POLYSACCHARIDE OF Streptococcus pneumoniae TYPE 19F
Sugawara, Tamio,Igarashi, Kikuo
, p. 195 - 208 (2007/10/02)
2-O--α,β-L-rhamnopyranose, a structural component of the capsular polysaccharide of Streptococcus pneumoniae type 19F, has been synthesized by sequential glycosylation reactions using the gl