319917-94-7

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 16848-19-4 1,2,5,6-di-O-isopropylidene-3-deoxy-3-amino-α-D-glucofuranoside 

Downstream Products

• 252052-98-5 3-deoxy-3-(N-allyl-p-toluenesulphonamido)-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 869064-94-8 3-deoxy-3-(2-bromobenzyl-para-toluenesulfonylamino)-1,2:5,6-di-O-isopropylidene-α-D-allofuranoside 
• 252053-06-8 N-allyl-N-[5-(1,2-dihydroxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-4-methyl-benzenesulfonamide 
• 200344-26-9 (5aR,6R,7R,8aR)-1-benzyl-5-p-toluenesulphonyl-1,3,3a,5a,6,7,8a,8b-octahydro-6,7-isopropylidenedioxy-4H-furo[2',3':5,6]pyrido[4,3-c]isoxazole 
• 200344-22-5 N-Allyl-N-((3aR,5S,6R,6aR)-5-formyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-4-methyl-benzenesulfonamide 
• 869064-95-9 3,5,6-trideoxy-3-(2-bromobenzyl-para-toluenesulfonylamino)-1,2-O-isopropylidene-α-D-ribo-hexenofuranoside 

Relevant academic research and scientific papers

Monosaccharide Derivatives as Anti-Inflammatory and/or Anti-Cancer Agents

The present invention relates to monosaccharide derivatives as anti-inflammatory agents. The compounds disorder herein can be useful for inhibition and prevention of inflammation and associated pathologies including inflammatory and autoimmune diseases su

MONOSACCHARIDE DERIVATIVES AS ANTI-INFLAMMATORY AND/OR ANTI-CANCER AGENTS

The present invention relates to monosaccharide derivatives as anti-inflammatory agents. The compounds disorder herein can be useful for inhibition and prevention of inflammation and associated pathologies including inflammatory and autoimmune diseases su

2-Benzazepine analogues from D-glucose: Synthesis of chiral cis- and trans-fused furo[3,2-c][2]benzazepine derivatives

Facile annulation of benzazepines onto furano-sugars has been achieved through Pd-catalyzed intramolecular cyclization. Using diisopropylidene D-glucose as a starting material, the first chiron approach to furobenzazepines in both cis and trans forms sele

Regioselective synthesis of chiral six- and seven-membered N- heterocycles from N-allyl carbohydrate nitrones: Tuning of regioselectivity by N-substitution

The intramolecular cycloaddifion of N-allyl carbohydrate nitrones leads to enantiomerically pure six- and seven-membered nitrogen heterocycles and the regio-selectivity of the cycloaddition was controlled by changing the substituent on the nitrogen atom of the N-allyl moiety.