870543-35-4

Upstream product

• 956116-09-9 4-azido-3-O-benzyl-6-desoxy-2-O-levulinoyl-α-D-glucopyranoside 
• 545-06-2 trichloroacetonitrile 

Downstream Products

• 1040140-52-0 C₆₁H₈₃N₃O₂₅ 
• 1239318-93-4 pent-4-enyl 4-azido-3-O-benzyl-4,6-dideoxy-2-O-levulinoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 943032-60-8 4-methoxyphenyl 4-azido-3-O-benzyl-4,6-dideoxy-2-O-levulinoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 870543-53-6 4-Oxo-pentanoic acid (2S,3R,4S,5R,6R)-2-[(2S,3R,4R,5S,6S)-3-acetoxy-5-benzyloxy-2-(4-methoxy-phenoxy)-6-methyl-tetrahydro-pyran-4-yloxy]-5-azido-4-benzyloxy-6-methyl-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

De novo asymmetric synthesis of the anthrax tetrasaccharide by a palladium-catalyzed glycosylation reaction

(Chemical Equation Presented) Choose your poison: In the de novo asymmetric synthesis of the anthrax tetrasaccharide 1 (25 steps from acetylfuran), the absolute configurations of three L sugars and one D sugar were set by the Noyori reduction of acetylfuran with the S,S and the R,R reagent, respectively. The configuration of the remaining carbohydrate unit was set by highly diastereoselective palladium-catalyzed glycosylation and post-glycosylation transformations.

ANTIBODIES FOR THE DETECTION OF BACILLUS ANTHRACIS AND VACCINE AGAINST B. ANTHRACIS INFECTIONS

35 Abstract The present invention relates to conjugates of oligosaccharides of formula 1, wherein R is a linker to a carrier protein and optionally comprises up to three further saccharides, 5 and which are useful for vaccination, methods of synthesis of