164729-41-3

Upstream product

• 100-39-0 benzyl bromide 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 147906-79-4 methyl 3,4-di-O-benzyl-6-O-tert.butyldimethylsilyl-2-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside 
• 164729-40-2 methyl 6-O-tert.butyldimethylsilyl-2-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 

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

Stereoselective Synthesis of Rare (D and L) Saccharides by a Facile Intramolecular Rearrangement of Hemiacetal Heptanolactone Alcohols

The hemiacetal heptanolactone alcohols 2a, b, c and d undergo a facile acid catalysed, stereospecific intramolecular rearrangement to yield the rare D and L saccharides 3, 4, 5 and 6 respectively.