89195-87-9

Upstream product

• 492-93-3 1,5-anhydro-D-mannitol 
• 100-52-7 benzaldehyde 
• 108-24-7 acetic anhydride 
• 89195-85-7 1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-mannitol 
• 154-58-5 1,5-anhydro-D-glucitol 
• 74720-63-1 1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-glucitol 

Downstream Products

• 89195-88-0 4,6-O-benzylidene-3-deoxy-3-nitro-D-allal 
• 74720-65-3 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol 
• 74720-66-4 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-erythro-hex-2-enitol 
• 116113-89-4 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-2-C-p-tolylsulfonyl-D-erythro-hex-2-enitol 
• 74720-70-0 (4aR,8R,8aS)-8-Nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 116113-85-0 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-C-nitro-2-C-p-tolylsulfonyl-D-glucitol 

Relevant academic research and scientific papers

PREPARATION OF 4,6-O-BENZYLIDENE-3-DEOXY-3-C-NITRO-D-GLUCAL AND D-ALLAL AND 1,5-ANHYDRO-4,6-O-BENZYLIDENE-2,3-DIDEOXY-3-C-NITRO-D-threo-HEX-2-ENITOL

Oxidation of 1,5-anhydro-D-mannitol with sodium metaperiodate, followed by nitromethane cyclization and benzylidenation afforded 1,5-anhydro-3-nitrohexitol derivatives having the D-gluco, D-manno, and D-galacto configurations.Conversion of the nitro alcoh

Stereochemistry of Nucleophilic Addition Reactions. VIII. Preparation of 1,5-Anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-erythro-hex-2-enitol and Its Reactions with Some Nucleophiles

The title compound was synthesized from 1,5-anhydro-D-glucitol via nitromethane cyclization.The reduction of the compound with sodium borodeuteride afforded a mixture of saturated nitro compounds having an axial and equatorial deuterium atom at C-2 in an