906360-08-5

Upstream product

• 906360-00-7 phenyl 3,4,6-tri-O-benzyl-2-O-(2,2-dimethyltrimethylene phosphonoyl)-β-D-thioglucopyranoside 
• 108-93-0 cyclohexanol 
• 4090-55-5 2-chloro-5,5-dimethyl[1,3,2]dioxaphosphinane 2-oxide 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Downstream Products

• 160412-84-0 cyclohexyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

PROCESS FOR PRODUCING 1,2-TRANS-GLYCOSIDE COMPOUND

In preparing a glycoside compound from (a) a furanose compound or pyranose compound, and (b) an alcohol compound, a process for preparing a glycoside compound in which glycosidic bond locates selectively trans form relative to C-2 hydroxyl group, the proc

Dialkylphosphates as stereodirecting protecting groups in oligosaccharide synthesis

(Chemical Equation Presented) Double duty: A phosphoric ester at the C2 position in glycosyl donors directs the glycosylation to occur selectively at the anomeric carbon atom with complete 1,2-trans selectivity. Since the phosphoric ester can be removed to give the hydroxy function, this group serves as a stereodirecting protecting group in oligosaccharide synthesis.