200344-27-0

Upstream product

• 622-30-0 N-benzyl hydroxylalmine 
• 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 
• 16848-19-4 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 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 
• 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 
• 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 

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.

Expeditious synthesis of chiral six and seven membered nitrogen heterocycles from carbohydrate amines by N-allyl carbohydrate nitrone cycloaddition: Tuning of regioselectivity by N-substitution

The cycloaddition of N-allyl carbohydrate nitrones leads to enantiomerically pure six and seven membered nitrogen heterocycles and the regioselectivity of the cycloaddition can be tuned by changing the substituent on the nitrogen atom.