18918-36-0

Upstream product

• 150-76-5 4-methoxy-phenol 
• 5160-09-8 2,3,4‐tri‐O‐acetyl-α-L‐rhamnopyranosyl chloride 
• 583040-99-7 4-methoxyphenyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 3615-41-6 L-Rhamnose 
• 18992-38-6 4-methoxyphenyl 2,3,4-tetra-O-acetyl-α-L-rhamnopyranoside 

Downstream Products

• 1028832-76-9 p-methoxyphenyl 2,3-O-cyclohexylidene-α-L-rhamnopyranoside 
• 1012786-50-3 (1'R)-p-methoxyphenyl 6-deoxy-2,3-O-(1-naphthyl)ethylidene-α-L-rhamnopyranoside 
• 1012786-57-0 p-methoxyphenyl 2,3-O-(2-naphthyl)ethylidene-α-L-rhamnopyranoside 
• 1012786-46-7 (1'R)-p-methoxyphenyl 6-deoxy-2,3-O-(2-naphthyl)ethylidene-α-L-rhamnopyranoside 
• 1012786-47-8 (1'S)-p-methoxyphenyl 6-deoxy-2,3-O-(2-naphthyl)ethylidene-α-L-rhamnopyranoside 
• 583041-06-9 4-methoxyphenyl 2-azido-3,4-di-O-acetyl-2-deoxy-α-L-fucopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 583041-07-0 4-methoxyphenyl 2-acetamido-3,4-di-O-acetyl-2-deoxy-α-L-fucopyranosyl-(1->3)-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 583041-08-1 4-methoxyphenyl 2-acetamido-3,4-di-O-acetyl-2-deoxy-α-L-fucopyranosyl-(1->3)-4,6-di-O-acetyl-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2,4-di-O-acetyl-α-L-rhamnopyranoside 
• 583041-04-7 4-methoxyphenyl 4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 583041-05-8 4-methoxyphenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 583041-02-5 4-methoxyphenyl 2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 583041-00-3 4-methoxyphenyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 583041-01-4 4-methoxyphenyl 4-O-benzoyl-α-L-rhamnopyranoside 
• 870543-36-5 4-methoxyphenyl 4-O-benzyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of aryl α-O-L-rhamnopyranoside by two-step reaction in one pot

The title compounds were conveniently synthesized by a phase transfer catalyzed approach in two steps and one pot using the rhamnopyranosyl chloride as key intermediate. The twostep one-pot procedure is more convenient and environmentally friendly, compared to the published synthetic routes. Besides, the structure-reactivity relationship and the plausible mechanism for this base-catalyzed glycosylation were discussed bymeans of the Hammett equation.

Efficient synthesis of a 6-deoxytalose tetrasaccharide related to the antigenic O-polysaccharide produced by Aggregatibacter actinomycetemcomitans serotype c

Concise synthesis of a 6-deoxy-α-l-talose tetrasaccharide, 6-deoxy-α-l-Talp-(1→3)-6-deoxy-α-l-Talp-(1→2)-6-deoxy-α-l-Talp-(1→3)-6-deoxy-α-l-Talp, the dimer of the disaccharide repeating unit of the OPS from Aggregatibacter actinomycetemcomitans serotype c

Using biological performance similarity to inform disaccharide library design

Designing better small-molecule discovery libraries requires having methods to assess the consequences of different synthesis decisions on the biological performance of resulting library members. Since we are particularly interested in how stereochemistry

Indium trichloride mediated cleavage of acetonides in the presence of acid-labile functional groups - Enhancing the synthetic utility of 1,3-dioxolanyl-substituted 1,2-oxazines

Indium trichloride in an acetonitrile-water mixture chemoselectively cleaved the isopropylidene acetals of various 1,3-dioxolanyl-substituted 1,2-oxazines as well as carbohydrate derivatives. Deprotection of acetonides can be achieved in substrates suscep

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

Total synthesis of antigen Bacillus anthracis tetrasaccharide - Creation of an anthrax vaccine candidate

Fighting Anthrax by recognizing its coat: The spores of Bacillus anthracis bear unique oligosaccharides on their surface for interaction with a host. These specific oligosaccharides may prove useful in the development of vaccines against this major biowar

Synthesis of the trisaccharide repeating unit of the O-antigen related to the enterohemorrhagic Escherichia coli type O26:H

L-Fucose was converted to the 2-azido-2-deoxy-L-fucose derivative, which together with the monosaccharide synthons prepared from L-rhamnose and D-glucosamine hydrochloride were utilized for the synthesis of the p-ethoxyphenyl glycoside of the trisaccharid