145260-87-3

Upstream product

• 10368-81-7 methyl 4-O-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 116-11-0 2-Methoxypropene 
• 79774-54-2 methyl 4-O-benzoyl-6-deoxy-α-D-glucopyranoside 
• 77-76-9 2,2-dimethoxy-propane 
• 98-88-4 benzoyl chloride 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 

Downstream Products

• 145260-85-1 C₄₉H₄₇NO₁₅ 
• 145260-84-0 C₄₄H₄₃NO₁₄ 
• 145260-75-9 C₄₄H₄₅NO₁₄ 
• 14133-63-2 methyl 6-deoxy-2,3-O-isopropylidene-α-D-glucopyranoside 
• 51288-33-6 methyl 3,4-di-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 
• 101068-99-9 methyl 2,3,4-tri-O-benzoyl α-L-rhamnopyranoside 
• 101068-96-6 Benzoic acid (2S,3S,4R,5R,6R)-4,5-diacetoxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 101068-97-7 Benzoic acid (2S,3S,4S,5R,6R)-4-acetoxy-5-hydroxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 101068-98-8 methyl 2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 89202-42-6 methyl 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 149827-71-4 1-O-acetyl-2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranose 
• 142967-71-3 methyl 2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranoside 
• 142967-72-4 2,4-di-O-benzoyl-3-O-bromoacetyl-α-L-rhamnopyranosyl chloride 

Relevant academic research and scientific papers

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

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

Structure and reactions of glycopyranoside derived dialdehydes

Several 4- protected D-glucopyranosides were synthesized and cleaved by sodium metaperiodate. Depending on the protection pattern the resulting dialdehydes showed different types of structures. Predominantly dioxane structures of the hemiacetal or hemiald

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 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.