911141-03-2

Upstream product

• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 79999-46-5 (4R,5S,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-2-one 

Downstream Products

• 1600532-85-1 (2S,3R,4R)-1-(2-(thiophen-2-yl)ethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine 
• 1129725-67-2 (2S,3R,4R)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1421781-90-9 (2S,3R,4R)-1-phenethyl-2-(hydroxymethyl)piperidine-3,4-diol 
• 1421781-96-5 (2S,3R,4R)-1-(4-methoxyphenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1421781-98-7 (2S,3R,4R)-1-(4-fluorophenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1600532-89-5 (2S,3R,4R)-1-(3-fluorophenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1600532-92-0 (2S,3R,4R)-1-(4-sulphonamidophenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1600532-93-1 (2S,3R,4R)-1-(4-methylphenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 
• 1600532-62-4 (2S,3R,4R)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-1-(furan-2-ylmethyl)piperidine 
• 1421782-05-9 (2S,3R,4R)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-1-phenethylpiperidine 
• 1421782-07-1 (2S,3R,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine 
• 1421782-09-3 (2S,3R,4R)-1-(4-fluorophenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine 
• 1600532-67-9 (2S,3R,4R)-1-(3-fluorophenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine 
• 1600532-69-1 (2S,3R,4R)-1-(2-(1H-imidazol-4-yl)ethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine 

Relevant academic research and scientific papers

A concise synthesis of N-substituted fagomine derivatives and the systematic exploration of their α-glycosidase inhibition

A novel and concise scheme has been developed successfully for the syntheses of N-substituted fagomine derivatives. The transformation of lactone (2) to 1,5-diol (3) was carried on with high yield (93-95%). The cyclization of 4 to 5 is a high stereoselect

A highly efficient and stereocontrolled synthesis of 2-deoxy-1,5- thioanhydro-L-hexitols from D-glycals in a tandem nucleophilic displacement reaction

2-Deoxy-1,5-thioanhydro-L-hexitols have been synthesized in a concise sequence that includes: i) ring opening of glycals with aqueous mercury(II) acetate/sodium borohydride; ii) mesylation of the free hydroxy groups of the multifunctionalized open interme