511543-92-3

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 100-39-0 benzyl bromide 
• 511543-91-2 6-O-(tert-butyldimethylsilyl)-1,2-O-isopropylidene-β-D-fructofuranose 
• 76549-76-3 1,2-O-Isopropylidene-β-D-fructofuranose 

Downstream Products

• 511543-94-5 1,3-bis[(3,4-di-O-benzyl-1,2-O-isopropylidene-β-D-fructofuranose-6-O-yl)methyl]benzene 
• 511543-97-8 1,4-bis[(3,4-di-O-benzyl-1,2-O-isopropylidene-β-D-fructofuranose-6-O-yl)methyl]benzene 
• 511544-00-6 1,2-bis[(3,4-di-O-benzyl-1,2-O-isopropylidene-β-D-fructofuranose-6-O-yl)methyl]benzene 
• 511544-01-7 3,4,3',4'-tetra-O-benzyl-6,6'-O-(o-xylylene)-di-α-D-fructofuranose 1,2':2,1'-dianhydride 
• 511544-02-8 3,4,3',4'-tetra-O-benzyl-6,6'-O-(o-xylylene)-di-β-D-fructofuranose 1,2':2,1'-dianhydride 
• 511543-93-4 2,3-di-O-benzyl-1,2-O-isopropylidene-β-D-fructofuranose 

Relevant academic research and scientific papers

Spacer-mediated synthesis of contra-thermodynamic spiroacetals: Stereoselective synthesis of C2-symmetric difructose dianhydrides

The xylylene moiety (ortho, meta, and para) was employed as a rigid tether in the spacer-mediated synthesis of difructose dianhydrides (DFAs), a unique class of bis-spiroacetal derivatives present in food products. The synthetic methodology exploits the s

Carbohydrate-derived spiroketals: Stereoselective synthesis of di-D-fructose dianhydrides via intramolecular aglycon delivery

(Matrix presented) A one-pot synthesis of C2-symmetric di-D-fructose dianhydrides having the 1,6,9,13-tetraoxadispiro [4.2.4.2]tetradecane skeleton has been accomplished via intramolecular aglycon delivery from (6 → 6) xylylene-tethered fructof