160636-37-3

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 251324-44-4 methyl 2-azido-2-deoxy-α-D-glucopyranoside 
• 273749-59-0 methyl 2-azido-2-deoxy-α/β-D-glucopyranoside 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 84048-43-1 2-acetamido-2-deoxy-α,β-D-glucopyranoside 
• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzilidene-α-D-mannopyranoside 
• 70774-92-4 methyl 4,6-O-benzylidene-2-O-p-toluenesulphonyl-α-D-glucopyranoside 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 146934-27-2 Methyl 2-azido-2-deoxy-3,4,6-tri-O-acetyl-1-thio-α-D-glucopyranoside 
• 173314-51-7 methyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranoside 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 

Downstream Products

• 173314-50-6 methyl O-<3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-α-D-galactopyranosyl>-(1<*>3)-2-azido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 325480-25-9 (R)-2-((2R,4aR,6S,7R,8R,8aS)-7-Azido-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionic acid methyl ester 
• 162678-87-7 Methyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 501088-18-2 methyl 2-azido-3-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-α-D-glucopyranoside 
• 1245566-97-5 C₂₇H₃₄N₁₀O₇ 
• 1245566-93-1 methyl (2-azido-2-deoxy-3-O-benzyl-6-deoxy-6-phthalimido-α-D-glucopyranosyl)-(1->4)-2,6-diazido-2,6-dideoxy-3-O-benzyl-α-D-glucopyranoside 
• 1245566-92-0 methyl (4-O-acetyl-2-azido-2-deoxy-3-O-benzyl-6-deoxy-6-phthalimido-α-D-glucopyranosyl)-(1->4)-2,6-diazido-2,6-dideoxy-3-O-benzyl-α-D-glucopyranoside 
• 1379976-86-9 C₃₇H₃₈N₁₀O₁₀ 
• 1379976-91-6 C₂₉H₃₄N₁₂O₈ 
• 1379976-89-2 C₂₉H₃₄N₁₂O₈ 
• 1245566-90-8 methyl 2,6-diazido-2,6-dideoxy-3-O-benzyl-β-D-glucopyranoside 
• 1245566-89-5 C₁₅H₂₁N₃O₇S 
• 325480-30-6 2-{2-[2-(7-azido-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionylamino]-propionylamino}-4-[1-[1-(1-methoxycarbonyl-ethylcarbamoyl)-ethylcarbamoyl]-5-(2,2,2-trifluoro-acetylamino)-pentylcarbamoyl]-butyric acid methyl ester 
• 325480-27-1 (R)-2-((2R,4aR,6S,7R,8R,8aS)-7-Azido-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionic acid 

Relevant academic research and scientific papers

Synthetic heparin pentasaccharides

Preparation and use of synthetic monosaccharides, disaccharides, trisaccharides, tetrasaccharides and pentasaccharides useful for the preparation of synthetic heparinoids.

AN EFFICIENT AND SCALABLE PROCESS FOR THE MANUFACTURE OF FONDAPARINUX SODIUM

The present invention relates to a process for the synthesis of the Factor Xa anticoagulent Fondaparinux and related compounds. The invention relates, in addition, to efficient and scalable processes for the synthesis of various intermediates useful in the synthesis of Fondaparinux and related compounds.

Oligo-Aminosaccharide compound

An oligo-aminosaccharide compound formed by binding 3 to 6 saccharides, such as 2,6-diamino-2,6-dideoxy-α-(1→4)-D-glucopyranose oligomers, or a salt thereof, which has high affinity to a double-stranded nucleic acid.

Synthesis of oligodiaminosaccharides having α-glycoside bonds and their interactions with oligonucleotide duplexes

Syntheses of the novel oligodiaminosaccharides, α-(1→4)-linked- 2,6-diamino-2,6-dideoxy-d-glucopyranose oligomers, and their interactions with nucleic acid duplexes DNA-DNA, RNA-RNA, and DNA-RNA are described. Monomers to tetramers of oligodiaminoglucose

Toward synthesis of the regular sequence of heparin: synthesis of two tetrasaccharide precursors

Two fully protected tetrasaccharides, which represent precursors for the synthesis of the regular sequence of heparin, were synthesized via coupling of a pair of disaccharide trichloroacetimidates with a thioglycoside and a glucosamine derivative, respectively, in a sequential manner.

Synthesis and biological evaluation of analogues of bacterial lipid I

Bacterial Lipid I analogues containing different anomeric groups at the muramic acid moiety were synthesized and screened in MurG enzyme assays run in the presence and absence of cell wall membranes. The results obtained in this study help elucidate the role of the lipid diphosphate in the recognition of Lipid I by MurG. (C) 2000 Elsevier Science Ltd.

Stereoselective preparation of alkyl glycosides of 2-acetamido-2-deoxy-α-D-glucopyranose by nonclassical halide-ion catalysis and synthesis and NMR spectroscopy of α-D-Gal p-(1-->3)-α-D-Glc pNAc-OMe

Keywords: Alkyl glycosides; 2-Acetamido-2-deoxy-α-D-glucopyranose; α-D-Gal p-(1 --> 3)-α-d-GlcpNAcOMe

Synthesis and two-dimensional nuclear magnetic resonance analysis of a tetra- and a hexa-saccharide fragment of the O-specific polysaccharide of Shigella dysenteriae type 1

The synthesis of the tetra- and hexa-succharide methyl glycosides α-D-Galp-(1-->3)-α-D-GlcpNAc-(1-->3)-α-L-Rhap-(1-->3)-α-L-Rhap-OMe (1), and α-L-Rhap-(1-->3)-α-L-Rhap-(1-->2)-α-D-Galp-(1-->3)-α-D-GlcpNAc-(1-->3)-α-L-Rhap-(1-->3)-α-L-Rhap-OMe (3) is descr