79083-38-8

Upstream product

• 79063-96-0 3,5-di-O-benzyl-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 79083-40-2 2,3,5-tri-O-benzyl-1-O-methyl-α-D-xylofuranoside 
• 67-56-1 methanol 
• 120693-82-5 3,5-Di-O-benzyl-α-D-xylofuranose 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 100-44-7 benzyl chloride 
• 22250-06-2 1,2-O-Cyclohexylidene-α-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 100-39-0 benzyl bromide 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 591727-19-4 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 908142-25-6 1-2 O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 34370-91-7 3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 100896-16-0 2,3,5-tri-O-benzyl-D-xylitol 
• 197716-45-3 3-Oxo-octanoic acid (S)-2-hydroxy-2-((4R,5R)-5-methoxymethoxy-2-phenyl-[1,3]dioxan-4-yl)-ethyl ester 
• 197716-46-4 3-Hexanoyl-4-((4R,5R)-5-methoxymethoxy-2-phenyl-[1,3]dioxan-4-yl)-5H-furan-2-one 
• 197716-43-1 3-Oxo-octanoic acid (2S,3R,4R)-2,3,5-tris-benzyloxy-4-methoxymethoxy-pentyl ester 
• 197716-41-9 tert-Butyl-diphenyl-((2S,3R,4R)-2,3,5-tris-benzyloxy-4-methoxymethoxy-pentyloxy)-silane 
• 32469-85-5 1,2-O-dimethyl-3,5-O-dibenzyl-α-D-xylofuranoside 
• 1612222-33-9 methyl-3,5-di-O-benzyl-2-O-(prop-2-ynyl)-α-D-xylofuranose 
• 1612222-57-7 6-(4-(methyl-3,5-di-O-benzyl-2-O-methylene-α-D-xylofuranose)-1H-1,2,3-triazol-1-yl)-6,7-dihydro-4H-[1,2,3]triazolo[5,1-c][1,4]-oxazine 
• 1612222-42-0 3-azido-1-(4-(methyl-3,5-di-O-benzyl-2-O-methylene-α-D-xylofuranose)-1H-1,2,3-triazol-1-yl)propan-2-ol 
• 208330-37-4 (2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-2-methoxy-dihydro-furan-3-one 
• 197716-38-4 2,3,5-tri-O-benzyl-1-O-methyl-D-xylofuranoside 

Relevant academic research and scientific papers

Synthesis, conformational analysis and biological studies of cyclic cationic antimicrobial peptides containing sugar amino acids

(Chemical Equation Presented) Sugar amino acid based 24-membered macrocyclic C2-symmetric cationic peptides were designed and synthesized. The cationic group was introduced in the sugar amino acids. The conformation of these cyclic compounds was ascertain

Novel D-xylose derivatives stimulate muscle glucose uptake by activating AMP-activated protein kinase α

Type 2 diabetes mellitus has reached epidemic proportions; therefore, the search for novel antihyperglycemic drugs is intense. We have discovered that D-xylose increases the rate of glucose transport in a non-insulin-dependent manner in rat and human myot

Alkylalanes and methyl furanosides: regioselective O-debenzylation or acetal cleavage

Perbenzylated methyl pentofuranosides were submitted to the action of three alkylalanes and regioselective debenzylation at O-2 of the four pentoses was observed when choosing the right match between anomeric configuration and aluminium reagent. Diisobuty

An epoxide derived from D-glucose as the key intermediate for penaresidine and sphingolipids synthesis

A multigram-scale synthesis of 3R,4R,5R 3,5-dibenzyloxy-4-p- methoxybenzyl-1,2-epoxypentane and its use as intermediate for sphingolipids, penazeridine and penazetidine synthesis are described.

Formal synthesis of (-)-syringolide 1 starting from D-xylose based on a biomimetic strategy

An expeditious and practical synthertic process for a nonproteinaceous elicitor, (-)-syringolide 1, has been developed in a short number of steps utilizing the putative biosynthetic pathway by featuring the elaboration of the protected D-xylose as a starting material.

The Use of Grignard Reagents in the Synthesis of Carbohydrates. III. The One-way Anomerization of Methyl Glycofuranosides and the Opening of Their Furanose Rings

The anomerization of methyl glycofuranoside derivatives with methylmagnesium iodide or t-butylmagnesium bromide occurred in a one-way manner.For example, methyl 5-O-benzyl-β-D-ribofuranoside (3β) was converted into the corresponding α-anomer (3α) in a 95p