79083-39-9

Upstream product

• 79063-96-0 3,5-di-O-benzyl-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 67-56-1 methanol 
• 161835-21-8 1,2-anhydro-3,5-di-O-benzyl-α-D-xylofuranose 
• 41341-99-5 3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 34370-91-7 3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 100-39-0 benzyl bromide 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 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 
• 161835-17-2 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose 
• 16054-77-6 3,5-di-O-benzyl-D-xylofuranose 
• 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 

Downstream Products

• 79083-38-8 1-O-methyl 3,5-di-O-benzyl α(D)xylo-pentoaldofuranose 
• 79063-91-5 (2R,3S,4S)-1,3-Bis-benzyloxy-5-methoxy-hexane-2,4-diol 
• 1040917-41-6 methyl 3,5-di-O-benzyl-2-O-(3,4-O-carbonate-6-O-benzoyl-2-deoxy-α-D-glucopyranosyl)-β-D-xylofuranoside 
• 1612222-58-8 6-(4-(methyl-3,5-di-O-benzyl-2-O-methylene-β-D-xylofuranose)-1H-1,2,3-triazol-1-yl)-6,7-dihydro-4H-[1,2,3]triazolo[5,1-c][1,4]-oxazine 
• 1612222-43-1 3-azido-1-(4-(methyl-3,5-di-O-benzyl-2-methylene-β-D-xylofuranose)-1H-1,2,3-triazol-1-yl)propan-2-ol, 
• 1612222-34-0 methyl-3,5-di-O-benzyl-2-O-(prop-2-ynyl)-β-D-xylofuranose 
• 1040917-54-1 methyl 3,5-di-O-benzyl-2-O-(3,4-O-carbonate-2,6-dideoxy-α-D-glucopyranosyl)-β-D-xylofuranoside 
• 32469-84-4 methyl-(O³,O⁵-dibenzyl-O²-methyl-β-D-xylofuranoside) 
• 161835-21-8 1,2-anhydro-3,5-di-O-benzyl-α-D-xylofuranose 
• 1041433-27-5 (2R,3S,4R,5R)-4-(benzyloxy)-5-(benzyloxymethyl)-2-methoxytetrahydrofuran-3-amine 
• 1041433-38-8 (2R,3R,4S,5R)-4-(benzyloxy)-5-(benzyloxymethyl)-2-methoxytetrahydrofuran-3-yl acetate 
• 91705-29-2 methyl 3,5-di-O-benzyl-2-O-octadecyl-β-D-xylofuranoside 
• 208330-40-9 (2R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-2-methoxy-dihydro-furan-3-one 
• 79063-97-1 (R)-3,5-Bis-benzyloxy-4-hydroxy-1-methoxy-pentan-2-one 

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

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.

Synthesis and glycosidic reaction of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers

Stereospecific synthesis of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers was successfully achieved via intramolecular SN2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonates, were prepared from the corresponding 1,2-diols and tosyl chloride under phase transfer conditions in good yields. Condensation of the anhydro sugars with 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose or N-benzyloxycarbonyl L-serine methyl ester in the absence of catalyst gave 1,2-trans-linked glycofuranosides in high yield.

A facile synthesis of 1,2-anhydroglycofuranose benzyl ethers

The synthesis of 1,2-anhydromanno-, -lyxo-, -gluco-, and -xylofuranose benzyl ethers was successfully achieved via intramolecular S(N)2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonate

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