153984-87-3

Upstream product

• 144367-27-1 3-O-allyloxycarbonyl-2-deoxy-4,6-O-isopropylidene-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 144367-32-8 4-methoxyphenyl 6-O-levulinoyl-2,3-di-O-p-toluoyl-β-D-glucopyranoside 

Downstream Products

• 153984-89-5 4-methoxyphenyl O-(2-deoxy-4,6-O-isopropylidene-2-phthalimido-β-D-glucopyranosyl)-(1<*>4)-6-O-levulinoyl-2,3-di-O-p-toluoyl-β-D-glucopyranoside 
• 213899-62-8 (3-O-allyloxycarbonyl-2-deoxy-4,6-O-isopropylidene-2-phthalimido-β-D-glucopyranosyl)-(1->4)-(6-O-levulinoyl-2,3-di-O-p-toluoyl-α-D-glucopyranosyl) trichloroacetimidate 

Relevant academic research and scientific papers

Synthesis of hyaluronic acid related di- and tetra-saccharides having a glucuronic acid at the reducing end

The synthesis is reported of 4-methoxyphenyl O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->4)-β-D-glucopyranosyluronic acid (1) and 4-methoxyphenyl O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->4)-O-(β-D-glucopyranosyluronic acid)-(1->3)-O-(2-acetamido-

Synthesis of a tetrasaccharide fragment of hyaluronic acid having a glucuronic acid at the reducing end

A stereocontrolled synthesis of a tetrasaccharide fragment of hyaluronic acid, β-p-methoxyphenyl glycoside of β-D-GlcNAc-(1→4)-β-D-GlcA-(1→3)-β-D-GlcNAc-(1→4)-D-GlcA, is presented.