846549-48-2

Upstream product

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

Downstream Products

• 869064-85-7 3-deoxy-3-(2-bromo-5-methoxybenzyl-para-toluenesulfonylamino)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranoside 
• 252053-08-0 N-allyl-N-[5-(1,2-dihydroxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-4-methyl-benzenesulfonamide 
• 200344-27-0 (5aS,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 
• 200344-23-6 N-Allyl-N-((3aR,5S,6S,6aR)-5-formyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-4-methyl-benzenesulfonamide 
• 850165-09-2 C₃₅H₅₀N₂O₁₄S₂ 
• 850165-11-6 N,N'-di-p-toluenesulfonyl-N,N'-bis(5-O-allyl-3-deoxy-1,2-O-isopropylidene-α-D-xylofuranos-3-yl)-1,3-diaminopropane 
• 850165-10-5 C₃₃H₄₆N₂O₁₂S₂ 
• 869064-87-9 3,5,6-trideoxy-3-(2-bromo-5-methoxybenzyl-para-toluenesulfonylamino)-1,2-O-isopropylidene-α-D-xylo-hexenofuranoside 
• 869064-86-8 3,5,6-trideoxy-3-(2-bromobenzyl-para-toluenesulfonylamino)-1,2-O-isopropylidene-α-D-xylo-hexenofuranoside 
• 869064-84-6 3-deoxy-3-(2-bromobenzyl-para-toluenesulfonylamino)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranoside 
• 850165-08-1 N,N'-di-p-toluenesulfonyl-N,N'-bis(3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranos-3-yl)-1,3-diaminopropane 
• 252053-00-2 3-deoxy-3-(N-allyl-p-toluenesulphonamido)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Relevant academic research and scientific papers

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.