186204-80-8

Upstream product

• 100-46-9 benzylamine 
• 186204-79-5 C₂₃H₃₀O₈S₂ 
• 177569-80-1 ((3aR,4S,6aS)-5-benzyl-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyrrol-4-yl)methanol 
• 75-16-1 methylmagnesium bromide 
• 186204-77-3 benzyl 2-deoxy-3,4-O-isopropylidene-2-C-methyl-β-L-ribopyranoside 
• 186204-78-4 2-deoxy-3,4-O-isopropylidene-2-C-methyl-L-ribitol 
• 123490-19-7 benzyl 2-deoxy-3,4-O-isopropylidene-2-methylene-β-L-erythro-pentopyranoside 

Downstream Products

• 779313-82-5 (3S,4R,5R)-1-Benzyl-5-methyl-piperidine-3,4-diol 

Relevant academic research and scientific papers

Synthesis of 1,4-imino-L-lyxitols modified at C-5 and their evaluation as inhibitors of GH38 α-mannosidases

A synthetic approach to 1,4-imino-L-lyxitols with various modifications at the C-5 position is reported. These imino-L-lyxitol cores were used for the preparation of a series of N-(4-halobenzyl)polyhydroxypyrrolidines. An impact of the C-5 modification on

Synthesis of a new potent α-fucosidase inhibitor

Enantiomerically pure (3S,4R,5R)-3,4-dihydroxy-5-methylpiperidine was prepared from L-arabinose and found to be a potent human placenta α-fucosidase inhibitor.