896729-57-0

Upstream product

• 1592-38-7 2-Naphthalenemethanol 
• 890131-34-7 2-naphthylmethyl O-(methyl 2,3-O-isopropylidene-4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 890131-35-8 2-naphthylmethyl O-(methyl 4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 890131-20-1 2-naphthylmethyl O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-(1->3)-4,6-di-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 890131-17-6 O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-(1->3)-4,6-di-O-acetyl-2-deoxy-2-trichloroacetamido-1-O-trichloroacetimidoyl-α-D-galactopyranose 
• 896729-54-7 2-naphthylmethyl O-(methyl 2,3-O-isopropylidene-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 896729-42-3 (2S,3S,4S,5R,6R)-3,4,5-Trihydroxy-6-[(2S,4aR,6R,7R,8R,8aR)-6-(naphthalen-2-ylmethoxy)-2-phenyl-7-(2,2,2-trichloro-acetylamino)-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy]-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 890131-32-5 O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-(1->3)-2-trichloromethyl-(4,6-di-O-acetyl-1,2-dideoxy-α-D-galactopyrano)[2,1-d]2-oxazoline 
• 890131-44-9 2-naphthylmethyl O-(methyl 3-O-benzoyl-4-O-levulinoyl-β-D-glucopyranosyluronate)-(1->3)-4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 541-88-8 Chloroacetic anhydride 

Relevant academic research and scientific papers

From polymer to size-defined oligomers: A highly divergent and stereocontrolled construction of chondroitin sulfate A, C, D, E, K, L, and M oligomers from a single precursor: Part 2

An efficient, stereocontrolled, and highly divergent approach for the preparation of oligomers of chondroitin sulfate (CS) A, C, D, E, K, L, and M variants, starting from a single precursor easily obtained by semisynthesis from abundant natural polymer is

From polymer to size-defined oligomers: An expeditious route for the preparation of chondroitin oligosaccharides

(Chemical Equation Presented) A synthetic short cut: Controlled acid hydrolysis of polymeric chondroitin sulfate affords a tailor-made disaccharidic fragment in good yield. This compound acts as a versatile starting material for the efficient construction