106848-97-9

Upstream product

• 115678-14-3 methyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 100-39-0 benzyl bromide 
• 115678-10-9 methyl 2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside 
• 115678-12-1 methyl 4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 115678-11-0 methyl 4-O-benzyl-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside 
• 115678-13-2 methyl 3,4-di-O-benzyl-6-deoxy-1-thio-α-L-mannopyranoside 
• 1245189-96-1 acetyl 2-O-acetyl-3,4-di-O-benzyl-L-rhamnoopyranoside 

Downstream Products

• 117249-17-9 3,4-di-O-benzyl-L-rhamnal 
• 1431974-53-6 benzyl (2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-2,3-di-O-benzyl-1-deoxy-1-(prop-2-enyl)-β-D-galactopyranuronate 
• 1431974-55-8 C₄₆H₅₂O₁₁ 
• 136633-01-7 Acetic acid (2R,3R,4R,5S,6S)-4,5-bis-benzyloxy-2-{2-[2-([1,3]dioxolan-2-ylmethoxy)-ethoxy]-ethoxy}-6-methyl-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

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

Synthesis of Oligosaccharides Corresponding to the Common Polysaccharide Antigen of Group B Streptococci

To facilitate mapping of the immunodominant region of the common polysaccharide antigen of group B streptococci, tetrasaccharide 1-O--α-rhamnopyranosyl>-D-glucitol (2) was synthesized in a stepwise fasion