127782-99-4

Upstream product

• 27954-10-5 methyl 2,3-O-isopropylidene-α-D-mannofuranoside 
• 26255-73-2 4-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole 
• 7757-38-2 2,3,5,6-di-O-isopropylidene-D-mannofuranose 
• 127782-98-3 C₁₇H₂₂O₇ 
• 124-63-0 methanesulfonyl chloride 
• 98-88-4 benzoyl chloride 

Relevant academic research and scientific papers

Stereospecific synthesis of C-arabinofuranosides and carba-disaccharide analogues of Motif C of cell wall AG complex of Mtb

A simple strategy for the synthesis of α- and β-C- arabinofuranosides featuring a furan ring transposition reaction has been developed. A novel double furan ring transposition reaction has proposed and executed for the synthesis of the carba-disaccharide

The endocyclic oxygen atom of D-mannopyranose is involved in its binding to pradimicins

Methyl 5-thio-α-D-mannopyranoside (1) and six inositols were evaluated for their ability to bind to pradimicins (PRMs) via molecular modeling and three binding assays. In all the experiments, the binding affinity of 1 was slightly lower than that of methy