74720-66-4

Upstream product

• 74720-63-1 1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-glucitol 
• 492-93-3 1,5-anhydro-D-mannitol 
• 89195-85-7 1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-mannitol 
• 100-52-7 benzaldehyde 
• 74720-64-2 2-O-acetyl-1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-glucitol 
• 154-58-5 1,5-anhydro-D-glucitol 
• 89195-87-9 2-O-acetyl-1,5-anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-D-mannitol 
• 74720-70-0 (4aR,8R,8aS)-8-Nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 89157-98-2 1,5-anhydro-4,6-O-benzylidene-3-deoxy-2-O-(methylsulfonyl)-3-nitro-D-glucitol 

Downstream Products

• 81105-84-2 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-C-(diacetylmethyl)-2-nitro-D-altritol 
• 81105-84-2 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-C-(diacetylmethyl)-2-nitro-D-glucitol 
• 84247-65-4 1,5:2,3-dianhydro-4,6-O-benzylidene-2-deoxy-2-nitro-D-mannitol 
• 84247-65-4 1,5:2,3-dianhydro-4,6-O-benzylidene-2-deoxy-2-nitro-D-allitol 
• 81105-85-3 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-2-nitro-D-ribitol 
• 81105-85-3 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-2-nitro-D-arabinitol 
• 116113-89-4 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-2-C-p-tolylsulfonyl-D-erythro-hex-2-enitol 
• 74720-65-3 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol 
• 74720-70-0 (4aR,8R,8aS)-8-Nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 81105-83-1 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-2-nitro-D-erythro-hex-2-enitol 
• 89195-88-0 4,6-O-benzylidene-3-deoxy-3-nitro-D-allal 
• 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

Preparation of Nitroalkenes from the Corresponding Nitroalkanes

Phenylselenenyl bromide reacts with nitroalkanes to give nitro(phenylseleno)alkanes and oxidative elimination provided nitroalkenes.

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