200344-30-5

Upstream product

• 622-30-0 N-benzyl hydroxylalmine 
• 200344-25-8 (3aR,5S,6R,6aR)-6-Allylamino-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 
• 876593-73-6 Allyl-[(3aR,5S,6aR)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[2,3-d][1,3]dioxol-(6E)-ylidene]-amine 
• 252053-01-3 (R)-1-((3aR,5S,6R,6aR)-6-Allylamino-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethane-1,2-diol 
• 252052-92-9 3-deoxy-3-allylamino-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 16848-19-4 1,2,5,6-di-O-isopropylidene-3-deoxy-3-amino-α-D-glucofuranoside 

Relevant academic research and scientific papers

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.

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.