544686-98-8

Upstream product

• 544686-94-4 1,2,3,4-tetra-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α/β-D-glucopyranose 
• 544687-08-3 1,2-O-isopropylidene-3-O-[6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-β-D-glucopyranosyl]-sn-glycerol 
• 98-88-4 benzoyl chloride 
• 544686-96-6 O-[6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-D-glucopyranosyl] trichloroacetimidate 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 912845-72-8 1,2-O-isopropylidene-3-O-[6-O-(β-D-glucopyranosyl)-β-D-glucopyranosyl]-sn-glycerol 

Relevant academic research and scientific papers

A Staphylococcus aureus lipoteichoic acid (LTA) derived structural variant with two diacylglycerol residues

Based on 1,2-O-isopropylidene-sn-glycerol five chiral building blocks containing differently modified glycerol residues were required for the synthesis of the target molecule 2. One of these building blocks is diacylglyceryl β-gentiobioside carrying a pho

Synthesis of the first fully active lipoteichoic acid

Nature outfoxed! Owing to the sensitivity of lipoteichoic acids (LTAs) to hydrolysis their biological activity could not be ascertained thus far. The chemical synthesis of LTA of Staphylococcus aureus 1, which contains hydrolytically labile D-alanine resi