85726-76-7

Upstream product

• 98-88-4 benzoyl chloride 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 77-76-9 2,2-dimethoxy-propane 
• 85726-75-6 Methyl-4-O-benzoyl-6-brom-6-desoxy-2,3-O-isopropyliden-α-D-mannopyranosid 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 122805-34-9 methyl 4-O-benzoyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannopyranoside 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 3162-96-7 methyl-4,6-O-phenylmethylene-α-D-mannopyranoside 
• 85761-43-9 Methyl 4,6-O-benzylidene-2,3-O-isopropylidene-α-D-mannopyranoside 
• 63167-69-1 methyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 122805-35-0 methyl 4-O-benzoyl-6-deoxy-6-iodo-2,3-isopropylidene-α-D-mannopyranoside 

Downstream Products

• 88331-96-8 methyl 2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 142967-72-4 2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranosyl chloride 
• 142967-71-3 methyl 2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranoside 
• 149827-71-4 1-O-acetyl-2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranose 
• 89202-42-6 methyl 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 101068-98-8 methyl 2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 101068-97-7 Benzoic acid (2S,3S,4S,5R,6R)-4-acetoxy-5-hydroxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 101068-96-6 Benzoic acid (2S,3S,4R,5R,6R)-4,5-diacetoxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 101068-99-9 methyl 2,3,4-tri-O-benzoyl α-L-rhamnopyranoside 
• 135129-62-3 methyl 3,4-di-O-benzoyl-2-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 51288-33-6 methyl 3,4-di-O-benzoyl α-L-rhamnopyranoside 
• 116013-26-4 Benzoic acid (3aS,4S,6R,7R,7aS)-4-methoxy-6-methyl-2-phenyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 122805-38-3 1,2,3-tri-O-acetyl-4-O-benzoyl-α-D-rhamnopyranose 
• 85726-77-8 4-O-Benzoyl-2-brom-2,6-didesoxy-3-O-formyl-α-D-clucopyranosylbromid 

Relevant academic research and scientific papers

Formation of aureolic acid oligodeoxy mono-, di-, and trisaccharides employing the dibromomethyl methyl ether reaction

2,3-Isopropylidene D-rhamnopyranoside 2 obtained from mannose was treated with dibromomethyl methyl ether to give 2,6-dideoxy-2-bromo-glucopyranosyl bromide 5. Correspondingly, the D-talo precursor 3 led to the epimeric galacto-pyranosyl bromide 4. Both g

GLYCOSAMINOGLYCAN (GAG) MIMETICS

The invention relates to compounds that are designed to mimic the structure of GAGs; methods for the preparation of the compounds; compositions comprising the compounds; and use of the compounds and compositions thereof for the anti-angiogenic, anti-metas

Synthesis of a D-rhamnose branched tetrasaccharide, repeating unit of the O-chain from Pseudomonas syringae pv. Syringae (cerasi) 435

The first synthesis of a D-rhamnose branched tetrasaccharide, corresponding to the repeating unit of the O-chain from Pseudomonas syringae pv. cerasi 435, as methyl glycoside is reported. The approach used is based on the synthesis of an opportune buildin

Deoxy and oxygen-substituted sugar-containing 14-aminosteroid compounds

Disclosed are 14-aminosteroid compounds, including pharmaceutically acceptable acid salts and esters thereof, useful in treating individuals afflicted with congestive heart failure, which compounds have the general formula: STR1 wherein R3 is a

Convergent synthesis of an octasaccharide fragment of the O-specific polysaccharide of Shigella dysenteriae type 1

A stereocontrolled, convergent synthesis is described of the linear octasaccharide methyl glycoside α-L-Rhap-(1 -> 2)-α-D-Galp-(1 -> 3)-α-GlcpNAc-(1 -> 3)-α-L-Rhap-(1 -> 3)-α-L-Rhap-(1 -> 2)-α-D-Galp-(1 -> 3)-α-D-GlcpNAc-(1 -> 3)-α-L-Rhap-OMe (11), which

SYNTHESIS OF A COMMON POLYSACCHARIDE ANTIGEN OF PSEUDOMONAS AERUGINOSA AS THE 6-AMINOHEXYL GLYCOSIDE

The synthesis is described of a tritylated 1,2-O-cyanoethylidene derivative (3) of the trisaccharide α-D-Rha-(1->2)-α-D-Rha-(1->3)-D-Rha.Triphenylmethylium perchlorate-catalysed polycondensation of 3 in the presence of 6-phthalimidohexyl 2,4-di-O-benzoyl-3-O-trityl-α-D-rhamnopyranoside followed by deprotection afforded the 6-aminohexyl glycoside of a D-rhamnan corresponding to a common polysaccharide antigen of Pseudomonas aeruginosa.

SYNTHESIS OF THE O-SPECIFIC POLYSACCHARIDE OF SHIGELLA FLEXNERI

A regular heteropolysaccharide built of tetrasaccharide repeating units is synthesised by means of regio- and stereospecific polycondensation of tritylated cyanoethylidene derivative.The polysaccharide obtained is identical with the O-antigenic polysaccharides of Shigella flexneri serotypes 3b, 3c, and variant Y.It also represents the basic chain of O-antigenic polysaccharides of all serotypes of this bacterium.

Synthesis of the Tetradeoxydisaccharide D-C of Aureolic Acids

Methyl 4-O-benzoyl-2,3-O-isopropylidene-α-D-rhamnopyranoside (3) is prepared in a straightforward way from methyl α-D-mannopyranoside, and reacts with dibromomethyl methyl ether to give the 2-bromo-2,6-dideoxy-α-D-glucopyranosyl bromide 7.Selective deform