22323-55-3

Upstream product

• 4005-46-3 (1R)-1-[(3aR,5R,6aR)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol 
• 98-59-9 p-toluenesulfonyl chloride 
• 75646-86-5 1,2-O-isopropylidene-5,6-O-methoxymethylidene-3-deoxy-D-erythro-3,4-hexofuranoside 
• 75646-85-4 3-p-toluenesulphonate of 1,2-O-isopropylidene-5,6-O-methoxymethylidene-α-D-glucofuranose 
• 3253-75-6 1,2:5,6-di-O-isopropylidene-3-O-tosyl-α-D-glucofuranoside 
• 76119-18-1 1,2-O-isopropylidene-5,6-O-methoxymethylidene-3-deoxy-α-D-xylohexofuranose 
• 2946-01-2 (3aR,5R,6S,6aR)-5-((R)-1,2-dihydroxyethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate 
• 2774-29-0 (3aR,5R,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 
• 6936-66-9 3-deoxy-D-xylo-hexono-1,4-lactone 
• 162427-40-9 3-deoxygalactose (α-furanose) 

Downstream Products

• 284031-37-4 1,3,6-trideoxy-1,6-imino-D-xylo-hexitol 

Relevant academic research and scientific papers

Syntheses of sugar-related trihydroxyazepanes from simple carbohydrates and their activities as reversible glycosidase inhibitors

Five diastereomeric trideoxy-1,6-iminohexitols were synthesised, and their inhibitory activities were determined against selected glycosidases. For comparison, 1,4,5-trideoxy-1,5-imino-D-lyxo-hexitol, the 4-deoxy derivative of 1-deoxymannojirimicin, was prepared by enzymatic isomerisation of 6-azido-3,6-dideoxy-D-ribo-hexose into the corresponding 2-ulose and subsequent hydrogenation accompanied by intramolecular reductive amination. (C) 2000 Elsevier Science Ltd.

Oxidation products of arachidonic acid. III. The synthesis of methyl 8R,9R,11R-, 8S,9R,11R-, and 8S,9S,11R-triacetoxyeicosa-5Z,12E,14Z-trienoate

A stereospecific synthesis of the title compounds, starting from readily available glucose derivatives, is described, and methods for differentiating them and the already reported 8R,9S,11R-eicosatrienoate are discussed.