869064-86-8

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 846549-48-2 N-[(3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-4-methyl-benzenesulfonamide 
• 16848-19-4 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 869064-84-6 3-deoxy-3-(2-bromobenzyl-para-toluenesulfonylamino)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranoside 

Relevant academic research and scientific papers

Stereoselective domino azidation and [3 + 2] cycloaddition: A facile route to chiral heterocyclic scaffolds from carbohydrate derived synthons

A rapid one pot intermolecular aryl azidation and intramolecular azide-olefin cycloaddition protocol has been designed using carbohydrate precursors to generate optically active, aziridine fused oxa-aza heterocycles, related to DNA targeting anti-tumour a

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