108865-15-2

Upstream product

• 110920-93-9 3,5-O-(R)-benzylidene-6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-glucofuranose 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 110920-92-8 (3aR,5R,6S,6aR)-5-((R)-2-(tert-butyldiphenylsilyloxy)-1-hydroxyethyl)-2,2-dimethyltetrahydrofuro(3,2-d)(1,3)dioxol-6-ol 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 78954-41-3 3,5-O-benzylidene-6,7-dideoxy-1,2-O-isopropylidene-7-nitro-α-D-gluco-hepto-1,4-furanose 
• 78954-40-2 3,5-O-benzylidene-7-deoxy-1,2-O-isopropylidene-7-nitro-α-DL-glycero-D-gluco-hepto-1,4-furanose 
• 78931-04-1 7-acetamido-3,5-O-benzylidene-6,7-dideoxy-9,11-O-ethylidene-1,2-O-isopropylidene-α-D-undeco-1,4-furanose 
• 78931-03-0 3,5-O-benzylidene-6,7-dideoxy-9,11-O-ethylidene-1,2-O-isopropylidene-7-nitro-α-D-undeco-1,4-furanose 
• 79026-20-3 7-acetamido-3,5-O-benzylidene-6,7-dideoxy-1,2:9,10:11,12-tri-O-isopropylidene-α-dodeco-1,4-furanose 
• 78954-42-4 3,5-O-benzylidene-6,7-dideoxy-1,2 : 9,10 : 11,12-tri-O-isopropylidene-7-nitro-α-dodeco-1,4-furanose 
• 125365-23-3 3,5-O-benzylidene-1,2-O-isopropylidene-6-O-(2-tetrahydropyranyloxyethyl)-α-<*>-glucofuranose 
• 111056-67-8 3,5-O-(S)-benzylidene-6-deoxy-6-iodo-1,2-O-isopropylidene-α-D-glucofuranose 
• 120191-68-6 (R)-2-((2R,3S,4R,5R)-3,4,5-Triacetoxy-tetrahydro-furan-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester 
• 115438-66-9 3,5-O-benzylidene-6,7-dideoxy-1,2-O-isopropylidene-8-O-mesyl-α-D-gluco-octose 
• 115465-59-3 8-azido-3-O-benzoyl-5-bromo-5,6,7,8-tetradeoxy-1,2-O-isopropylidene-β-L-ido-octose 
• 115438-64-7 ethyl 3,5-O-benzylidene-6,7-dideoxy-1,2-O-isopropylidene-α-D-gluco-octuronate 
• 115438-65-8 3,5-O-benzylidene-6,7-dideoxy-1,2-O-isopropylidene-α-D-gluco-octose 
• 115649-93-9 1-deoxy-castanospermine 

Relevant academic research and scientific papers

SPECIFIC SYNTHESIS AND STEREOCHEMICAL ASSIGNMENT OF THE DIASTEREOMERIC 3,5-O-BENZYLIDENE-1,2-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE ISOMERS

Pyridinium tosylate-catalysed acetal exchange between benzaldehyde dimethyl acetal and 6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-glucofuranose was investigated as an alternative to the original procedure of Brigl and Gruener (condensation of