55174-94-2

Upstream product

• 25791-21-3 3-benzyloxycarbonylamino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allo-1,4-furanose 
• 37073-89-5 3-benzyloxycarbonylamino-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 25834-61-1 ((3aR,5S,6R,6aR)-5-Formyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-carbamic acid benzyl ester 
• 28072-60-8 3-azido-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 14125-95-2 3-amino-3-deoxy-1,2-O-(1-methylethylidene)-α-D-xylofuranose 
• 501-53-1 benzyl chloroformate 
• 28072-61-9 3-azido-3-deoxy-1,2-O-isopropylidene-α-D-xylo-pentodialdo-1,4-furanose 

Downstream Products

• 55174-96-4 3-benzyloxycarbonylamino-3-deoxy-5-O-p-toluenesulphonyl-1,2-O-isopropylidene-α-D-ribofuranose 

Relevant academic research and scientific papers

Synthesis of polyhydroxylated azetidine iminosugars and 3-hydroxy-N-methylazetidine-2-carboxylic acid from d-glucose

The azetidine iminosugars, (2S,3R)-2-((R)-1,2-dihydroxyethyl)azetidin-3-ol 3, (2R,3R)-2-(hydroxymethyl)azetidin-3-ol 4, and (2S,3R)-3-hydroxy-N-methylazetidine-2-carboxylic acid 5 were synthesized from d-glucose derived 3-N-benzyloxycarbonyl-3-deoxy-1,2-O

Synthesis, conformational study, glycosidase inhibitory activity and molecular docking studies of dihydroxylated 4- and 5-amino-iminosugars

An efficient methodology for the synthesis of new amino iminosugars 6a, 7a and 8, starting from d-glucose, is reported. The conformational study using 1H NMR data showed that the amino iminosugar 6a exists in the 2C5 while