170898-57-4

Upstream product

• 2595-05-3 Diacetone D-glucose 
• 33746-39-3 3-O-allyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 156742-37-9 (R)-1-[(3aR,5R,6R,6aR)-6-(allyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol 
• 622-30-0 N-benzyl hydroxylalmine 
• 156854-15-8 (3aR,5S,6R,6aR)-6-Allyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 

Downstream Products

• 952715-86-5 (1R,2R,4R,5R,6R,9S)-5-acetoxy-11-benzyl-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3,7,10-trioxa-11-aza-tricyclo[7.2.1.0^2,6]dodecane 

Relevant academic research and scientific papers

Synthesis of chiral oxepanes and pyrans by 3-O-allylcarbohydrate nitrone cycloaddition (3-OACNC)

3-O-Allylcarbohydrate nitrone cycloaddition (3-OACNC) furnished pyran and oxepane derivatives from 3-O-allyl hexose N-benzyl nitrones and 3-O-allyl furanoside-5-aldehyde N-benzyl/methyl nitrones. The regioselectivity of 3-OACNC was found to depend on the

Synthesis of enantiomeric pyrans from a 3-O-allylallose derivative by the application of intramolecular nitrone cycloaddition

The intramolecular nitrone cycloaddition of three sets of 3-O-allylpyranose and the corresponding homochiral 3-O-allylfuranose-5-aldehyde derivatives was studied; one set derived from D-allose gave rise to only pyran derivatives which were converted to en