164729-47-9

Upstream product

• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 164729-44-6 methyl 2,4-di-O-benzyl-6-O-tert.butyldimethylsilyl-3-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside 
• 164729-45-7 methyl 2,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside 
• 164729-43-5 methyl 6-O-tert.butyldimethylsilyl-3-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside 
• 164729-42-4 methyl 3-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside 
• 126330-73-2 2-pyridyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 164729-46-8 methyl 2,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-6-O-(p-tolylsulfonyl)-α-D-glucopyranoside 

Downstream Products

• 164729-49-1 (3S,4S,5R,6R)-5-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-4,6-di(benzyloxy)-7-heptanolide 

Relevant academic research and scientific papers

Stereoselective synthesis of rare (D and L) mono and disaccharides of 5-deoxy hexofuranosiduronic acids by a facile intramolecular rearrangement of hemiacetal heptanolactone alcohols

Transformation of D-glucose, 2-O-, 3-O- and 4-O-linked disaccharides 6,7 and 35 to the corresponding cyclohexanone alcohols 1a/b, 17, 18, 29, 30 and 36 respectively is described. Stereospecific conversion of these cyclohexanone alcohols to the correspondi