910479-41-3

Upstream product

• 16848-19-4 1,2,5,6-di-O-isopropylidene-3-deoxy-3-amino-α-D-glucofuranoside 
• 25791-21-3 3-benzyloxycarbonylamino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allo-1,4-furanose 
• 1346679-03-5 3-[(allyl)(benzyloxycarbonyl)amino]-3-deoxy-1,2-O-isopropylidene-α-D-allo-1,4-furanose 
• 1346679-02-4 3-[(allyl)(benzyloxycarbonyl)amino]-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allo-1,4-furanose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 35085-25-7 3-azido-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 
• 910479-44-6 ((3aR,5R,6R,6aR)-2,2-Dimethyl-5-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-carbamic acid benzyl ester 
• 106-95-6 allyl bromide 
• 21870-78-0 3-azido-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 37073-89-5 3-benzyloxycarbonylamino-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 

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 
• 1346679-04-6 C₁₄H₁₇NO₄ 
• 448896-88-6 (8R,8aS)-8-hydroxy-8,8a-dihydro-1H-oxazolo[3,4-a]pyridin-3(5H)-one 

Relevant academic research and scientific papers

Chiron approach strategy to the bicyclic oxazolidinylpiperidine: A building block for preparing mono-and bi-cyclic iminosugars

A chiron approach to the synthesis of bicyclic oxazolidinylpiperidine, a synthetically potential building block for preparing mono-and bi-cyclic iminosugars, is reported from D-glucose using ring closing metathesis as the key step.

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.