200344-23-6

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 252053-00-2 3-deoxy-3-(N-allyl-p-toluenesulphonamido)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 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 
• 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 

Downstream Products

• 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 

Relevant academic research and scientific papers

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.