140223-69-4

Upstream product

• 115259-73-9 3-O-benzyl-5-deoxy-5-C-<(E)-7-deoxy-1,2:3,4-di-O-isopropylidene-L-glycero-α-D-galacto-heptopyranos-7-ylidene>-1,2-O-isopropylidene-α-D-xylofuranose 
• 140138-22-3 3-O-benzyl-6-C-(1,2:3,4-di-O-isopropylidene-α-D-galacto-hexopyranos-6-ulos-6-yl)-1,2-O-isopropylidene-D-glycero-β-L-ido-hexofuranose 
• 115259-73-9 3-O-benzyl-5-deoxy-5-C-<(E)-7-deoxy-1,2:3,4-di-O-isopropylidene-D-glycero-α-D-galacto-heptopyranos-7-ylidene>-1,2-O-isopropylidene-α-D-xylofuranose 

Relevant academic research and scientific papers

Stereoselective Synthesis of Higher Sugar Dialdoses via Coupling of Terminal C-Atoms of Simple Monosaccharides

Different methods of the preparation of the precursors of higher carbon sugars via the coupling of monosaccharide sub-units are presented. The "economic" synthesis of such precursor is exemplified by the preparation of enone 11. Functionalization of the a

Peparation of higher-carbon sugars by stereoselective osmylation of related allylic alcohols

The catalytic osmylation of the following higher-carbon sugar allylic alcohols and enones was examined. 3-O-Benzyl-5-deoxy-5-C--1,2-O-isopropylidene-α-D-xylofuranose (5) af