142967-71-3Relevant academic research and scientific papers
Convergent synthesis of an octasaccharide fragment of the O-specific polysaccharide of Shigella dysenteriae type 1
Pozsgay, Vince,Pannell, Lewis
, p. 105 - 122 (2007/10/02)
A stereocontrolled, convergent synthesis is described of the linear octasaccharide methyl glycoside α-L-Rhap-(1 -> 2)-α-D-Galp-(1 -> 3)-α-GlcpNAc-(1 -> 3)-α-L-Rhap-(1 -> 3)-α-L-Rhap-(1 -> 2)-α-D-Galp-(1 -> 3)-α-D-GlcpNAc-(1 -> 3)-α-L-Rhap-OMe (11), which
Stereoselective syntheses of a di-, tri-, and tetra-saccharide fragment of Shigella dysenteriae type 1 O-antigen using 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl chloride as a glycosyl donor
Pavliak,Kovac,Glaudemans
, p. 103 - 116 (2007/10/02)
Methyl 2,4-di-O-benzoyl-α-L-rhamnopyranoside (1) furnished a crystalline 3-O-bromoacetyl derivative that was treated with the dichloromethyl methyl ether-ZnCl2 reagent to give 2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranosyl chloride (3). C
