551960-79-3

Upstream product

• 148703-40-6 6-deoxy-6-N-phenylmethylamino-1,2-O-isopropylidene-3-O-phenylmethyl-α-D-gluco-1,4-furanose 
• 35781-78-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 19877-13-5 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-enofuranose 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 41545-33-9 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-6-nitro-α-D-gluco-furanose 
• 501-53-1 benzyl chloroformate 
• 24384-87-0 6-amino-6-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 130790-29-3 1,6-dideoxy-1,6-imino-(2S,3R,4R,5R)-D-glucitol 

Relevant academic research and scientific papers

Short and efficient synthesis of (2S,3R,4R,5R) and (2S,3R,4R,5S)-tetrahydroxyazepanes via the Henry reaction

The Henry reaction with the easily available α-d-xylo-pentodialdose afforded a diastereomeric mixture of nitroaldoses with the α-d-gluco- and β-l-ido-configuration, respectively, in good yield. When n-BuLi was used as the base, the reaction afforded the α

Concise and practical synthesis of (2S,3R,4R,5R) and (2S,3R,4R,5S)-1,6-dideoxy-1,6-iminosugars

The syntheses of (2S,3R,4R,5R) and (2S,3R,4R,5S)-1,6-dideoxy-1,6 iminosugars 1a and 1b, respectively, from D-glucose are described. The key transformations in this reaction sequence include regio-selective epoxide ring opening with N-benzylamine followed