910479-44-6

Upstream product

• 37073-89-5 3-benzyloxycarbonylamino-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 300572-61-6 (R)-1-((3aR,5S,6R,6aR)-6-Amino-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethane-1,2-diol 
• 35085-25-7 3-azido-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 21870-78-0 3-azido-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 910479-39-9 (3aR,3bR,7aR,8aR)-2,2-Dimethyl-3a,5,7a,8a-tetrahydro-3bH-1,3,8-trioxa-4-aza-cyclopenta[a]indene-4-carboxylic acid benzyl ester 
• 910479-37-7 (3aR,3bR,6R,7R,7aS,8aR)-6,7-Dihydroxy-2,2-dimethyl-hexahydro-1,3,8-trioxa-4-aza-cyclopenta[a]indene-4-carboxylic acid benzyl ester 
• 910479-47-9 (2S,3S,4S,5R)-4,5-Bis-benzyloxy-3-hydroxy-2-hydroxymethyl-piperidine-1-carboxylic acid benzyl ester 
• 910479-46-8 (3R,3aS,6R,7R,7aS)-6,7-Bis-benzyloxy-2,3-dihydroxy-hexahydro-furo[3,2-b]pyridine-4-carboxylic acid benzyl ester 
• 910479-45-7 (3aR,3bR,6R,7R,7aS,8aR)-6,7-Bis-benzyloxy-2,2-dimethyl-hexahydro-1,3,8-trioxa-4-aza-cyclopenta[a]indene-4-carboxylic acid benzyl ester 
• 1620809-06-4 (R)-1-[(2R,3R)-3-acetoxy-1-(benzyloxycarbonyl)-5-(1,2-dihydroxyethyl)-1,2,3,6-tetrahydropyridin-2-yl]ethane-1,2-diyl diacetate 
• 1620809-07-5 (R)-1-[(2R,3R)-3-acetoxy-5-(acetoxymethyl)-1-(benzyloxycarbonyl)-1,2,3,6-tetrahydropyridin-2-yl]ethane-1,2-diyl diacetate 
• 1620809-08-6 C₂₂H₂₅NO₉ 
• 1620809-09-7 (2S,3S,4S,5S)-5-(acetoxymethyl)-1-(benzyloxycarbonyl)-2-[(R)-1,2-bis(acetoxyethyl)]piperidine-3,4,5-triyl triacetate 
• 1620809-10-0 C₂₄H₃₁NO₁₂ 
• 1620809-12-2 benzyl (5R,6S)-5-acetoxy-6-(acetoxymethyl)-3-vinyl-5,6-dihydropyridine-1(2H)-carboxylate 
• 1620809-13-3 C₁₆H₁₉NO₄ 
• 1620809-14-4 benzyl (5R,6S)-5-acetoxy-6-(acetoxymethyl)-3-(1,2-dihydroxyethyl)-5,6-dihydropyridine-1(2H)-carboxylate 
• 1620809-15-5 benzyl (5R,6S)-5-acetoxy-3,6-bis(acetoxymethyl)-5,6-dihydropyridine-1(2H)-carboxylate 

Relevant academic research and scientific papers

A general strategy for the stereoselective synthesis of l-1-deoxyallonojirimycin and d-1-deoxygulonojirimycin

A general strategy for the synthesis of deoxyazasugars from d-glucose is described. Ring-closing metathesis and stereoselective dihydroxylation reactions were used as key steps.