136172-67-3

Upstream product

• 89064-71-1 β-C-(hydroxymethyl)-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose 
• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 240137-98-8 3-((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-yn-1-ol 
• 136088-98-7 methyl 3-(2,3,4,6-O-tetrabenzyl-β-D-glucopyranosyl)propenoate 

Downstream Products

• 136172-75-3 (1R,2R)-1-(2,3,4,6-O-tetrabenzyl-β-D-glucopyranosyl)-1-deuteriopropane-2,3-diol 
• 136172-76-4 (1S,2S)-1-(2,3,4,6-O-tetrabenzyl-β-D-glucopyranosyl)-1-deuteriopropane-2,3-diol 

Relevant academic research and scientific papers

A concise synthesis of 3-hydroxy-4-β-glucopyranosyl) benzoate: A new route to β-C-aryl glycosides

A synthesis of specifically substituted β-C-aryl glycosides is described. The aromatic moiety is built up starting from the easily available 2,3,4,6-tetra-O-benzyl-D-gluconolactone with a benzoannulation reaction as a key step.

Preferred Conformation of C-Glycosides. 6. Conformational Similarity of Glycosides and Corresponding C-Glycosides

The conformation of the α-(axial)-C-glycosides 1-3 and the β-(equatorial)-C-glycosides 4-6 were studied by 1H NMR.Their preferred solution conformation was found to match that of the corresponding parent glycosides.The study of 2-deoxy compounds 13-16 sho