73983-19-4

Upstream product

• 72657-01-3 1,2-O-(1-methoxyethylidene)-3,4-di-O-benzyl-β-L-rhamnopyranose 
• 2754-27-0 trimethylsilyl acetate 
• 69558-07-2 methyl-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 108-24-7 acetic anhydride 
• 79080-88-9 3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose 
• 73983-18-3 2-O-acetyl-3,4-di-O-benzyl-L-rhamnopyranose 
• 69980-52-5 2,3,4-tri-O-acetyl-L-rhamnopyranosyl bromide 
• 100-44-7 benzyl chloride 
• 30021-94-4 1,2,3,4-O-tetraacetyl-α-L-rhamnopyranose 
• 141554-87-2 3,4-Di-O-Acetyl-β-L-rhamnose 1,2-(ethylorthoacetate) 
• 1431974-50-3 C₁₀H₁₈O₆ 
• 78161-49-6 3,4-di-O-benzyl-6-deoxy-1-thio-L-mannopyranose 
• 245450-63-9 2,3-di-O-benzyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 
• 125590-93-4 2,3-di-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 

Downstream Products

• 112107-26-3 methyl (3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 112107-25-2 (2S,3R,4S,5S,6S)-4,5-Bis-benzyloxy-2-[(2S,3R,4R,5S,6S)-4,5-bis-benzyloxy-2-((2R,3R,4R,5S,6S)-4,5-bis-benzyloxy-2-methoxy-6-methyl-tetrahydro-pyran-3-yloxy)-6-methyl-tetrahydro-pyran-3-yloxy]-6-methyl-tetrahydro-pyran-3-ol 
• 176168-84-6 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 167013-82-3 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 176168-83-5 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 176168-85-7 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 176168-86-8 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-2-O-[3,4-di-O-benzyl-2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside 
• 112107-28-5 methyl 3,4-di-O-benzyl-2-O-<3,4-di-O-benzyl-2-O-(α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 148431-63-4 O-(3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl)-(1->6)-1,2;3,4-di-O-isopropylidene-α-D-galactopyranose 
• 138098-80-3 1,2-anhydro-3,4-di-O-benzyl-6-deoxy-β-L-mannopyranose 
• 73983-18-3 2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranoside 
• 72599-87-2 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl chloride 

Relevant academic research and scientific papers

Efficient synthesis of O-antigen fragments expressed by Burkholderia anthina by modular synthesis approach

To facilitate mapping of the interaction region of the O-chain of the lipopolysaccharide from Burkholderia anthina and of a lipopolysaccharide-specific monoclonal antibody, trisaccharide propyl α-l-rhamnopyranosyl-(1→2)-α-d-galactopyranosyl-(1→3)-α-l-rham

C-Glycoside D-galacturonates suitable as glycosyl acceptors for the synthesis of allyl C-homo- and rhamno-galacturonan modules

Methyl 2,3-di-O-benzyl-1-deoxy-1-(prop-2-enyl)-α-D- galactopyranuronate and benzyl 2,3-di-Obenzyl- 1-deoxy-1-(prop-2-enyl)-α- D-galactopyranuronate were prepared as glycosyl acceptors. The glycosyl donors benzyl 4-O-acetyl-2,3-di-O-benzyl-1-(trichloroacet

Combination of solid phase and solution phase synthesis of oligosaccharides using sonication

An approach that combines solid phase and solution phase synthesis of oligosaccharides via the assistance of sonication has been developed. By employing the traceless linker, the designed oligosaccharides can be obtained in pure form and, more importantly

Synthesis of the trisaccharide α-L-Rha-(1-2)-α-L-Rha-(1-2)-α-L-Rha with a dioxolane-type spacer-arm

The trisaccharide α-L-Rha-(1-2)-α-L-Rha-(1-2)-α-L-Rha with a dioxolane-type spacer was obtained by using the trichloroacetimidate method in all of the glycosidation steps. After deprotection, the trisaccharide was coupled to BSA or KLH by reductive aminat

Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses

1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-

CARBOHYDRATE COMPONENTS OF FLAVONOL TRIAOSIDES: A CONVENIENT SYNTHESIS OF O-α-L-RHAMNOPYRANOSYL-(1->3)-O-α-L-RHAMNOPYRANOSYL-(1->6)-D-GALACTOSE AND-O-α-RHAMNOPYRANOSYL-(1->6)-D-GALACTOSE

Condensation of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose (1) with 2,4-di-O-acetyl-3-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl bromide (2), followed by subsequent removal of the isopropylidene and acetyl groups from the product,