1364662-63-4

Upstream product

• 1380592-26-6 C₄₇H₆₇N₃O₁₅Si 
• 545-06-2 trichloroacetonitrile 
• 243982-79-8 methyl (dimethylthexylsilyl 3-O-benzyl-β-L-idopyranoside)uronate 

Downstream Products

• 1364662-70-3 methyl 4-O-(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-levulinoyl-α-D-glucopyranosyl)-1,5-anhydro-3-O-benzyl-2-O-pivaloyl-L-xylo-hex-1-enitoluronate 
• 1364662-72-5 N-benzyloxycarbonyl-2-aminoethyl(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-levulinoyl-α-D-glucopyranosyl)(1->4)(methyl 3-O-benzyl-2-O-pivaloyl-α-L-idopyranosyluronate)(1->4)(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranosyl)(1->4)(methyl 3-O-benzyl-2-O-pivaloyl-α-L-idopyranosyluronate)(1->4)(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranosyl)(1->4)methyl 3-O-benzyl-2-O-pivaloyl-α-L-idopyranosiduronate 
• 1266234-48-3 N-benzyloxycarbonyl-2-aminoethyl-4-O-(2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-3-O-benzyl-α-L-idopyranosiduronic acid 
• 1364662-74-7 methyl (N-benzyloxycarbonyl-2-aminoethyl4-O-(6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-3-O-benzyl-2-O-pivaloyl-α-L-idopyranoside)uronate 
• 1364662-68-9 methyl (N-benzyloxycarbonyl-2-aminoethyl 4-O-(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranosyl)-3-O-benzyl-2-O-pivaloyl-α-L-idopyranoside)uronate 
• 1364662-69-0 N-benzyloxycarbonyl-2-aminoethyl(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-levulinoyl-α-D-glucopyranosyl)(1->4)(methyl 3-O-benzyl-2-O-pivaloyl-α-L-idopyranosyluronate)(1->4)(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranosyl)(1->4)methyl 3-O-benzyl-2-O-pivaloyl-α-L-idopyranosiduronate 
• 1364662-67-8 methyl (N-benzyloxycarbonyl-2-aminoethyl 4-O-(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-levulinoyl-α-D-glucopyranosyl)-3-O-benzyl-2-O-pivaloyl-α-L-idopyranoside)uronate 

Relevant academic research and scientific papers

Synthesis of amine-functionalized heparin oligosaccharides for the investigation of carbohydrate-protein interactions in microtiter plates

The synthesis of well-defined oligosaccharides is crucial for the establishment of structure-activity relationships for specific sequences of heparin, contributing to the understanding of the biological role of this polysaccharide. It is highly convenient