81692-26-4

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 76679-50-0 1,2-O-isopropylidene-3-O-(2,3,4-tri-O-benzyl-β-D-glucocpyranosyl)-sn-glycerol 
• 47727-93-5 2,3,4-tri-O-benzyl-D-glucopyranose 
• 22323-82-6 (S)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)methanol 
• 76679-39-5 [(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl trifluoromethanesulfonate 

Downstream Products

• 81739-23-3 1,2-O-isopropylidene-3-O-<6-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-2,3,4-tri-O-benzyl-β-D-glucopyranosyl>-sn-glycerol 

Relevant academic research and scientific papers

A simple approach to the syntheesis of a membrane teichoic acid fragment of Staphylococcus aureus

The triflate procedure of Schimdt at al. enabled us to synthesize the glycolipid, 1,2-di-O-stearoyl-3-O--sn-glycerol.Phorphsorylation of this compound with an activated and properly protected phosphatidyl derivative gave a phosphotriester derivative which, after deblocking of all protective grouops, afforded a naturally occurring teichoic acid fragment.