134341-61-0

Upstream product

• 4983-69-1 (4aR)-6c-Methoxy-2c-phenyl-(4ar,9at)-hexahydro-[1,3]dioxino[5,4-e][1,4]dioxepin-7ξ,9ξ-diol 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 131433-03-9 methyl 4,6-O-benzylidene-β-D-galactopyranoside 

Downstream Products

• 3162-96-7 (2R,4aR,6R,7S,8R,8aR)-6-Methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 131433-03-9 methyl 4,6-O-benzylidene-β-D-galactopyranoside 
• 3162-96-7 methyl-4,6-O-benzylidene-β-D-gulopyranoside 
• 2484-81-3 methyl-[O²-acetyl-3-acetylamino-O⁴,O⁶-((R)-benzylidene)-3-deoxy-α-D-glucopyranoside] 
• 99745-99-0 methyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 101223-51-2 methyl 4,6-O-benzylidene-3-deoxy-3-phenylazo-α-D-glucopyranoside 
• 1534-21-0 glyoxal bis(phenylhydrazone) 
• 1426264-12-1 C₂₀H₂₂N₂O₅ 

Relevant academic research and scientific papers

Toward fluorinated aminoglycosides: Structural studies of phenylhydrazine condensation with carbohydrate derivatives

The reaction of phenylhydrazine with a sugar dialdehyde in water, as a key step for the synthesis of the 3-amino-3-deoxy-d-glucose moiety contained in kanamycin, has been revisited. Structural studies (IR and NMR as well as a simple theoretical model base

Synthesis and NMR spectroscopic analysis of 3-nitro-pyranoside, 3-nitro-septanoside and 4-nitro-septanoside derivatives by condensation of the anion of nitromethane with glycoside dialdehydes

The utility of the nitroaldol reaction for accessing 3-nitro-pyranoside, 3-nitro-septanoside or 4-nitro-septanoside derivatives, by reaction of the anion of nitromethane with glycoside dialdehydes is demonstrated. Initially, the feasibility of using unpro

The stereocontrolled formation of cyclic vicinal cis-diols via a samarium diiodide pinacol coupling of dialdehydes

Aliphatic 1,5- and 1,6 dialdehydes with and without α-substituents, as well as derivatives of carbohydrate dialdehydes undergo a pinacol coupling reaction in the presence of SmI2 to give cis-diols as the preponderant products. When α-alkoxy groups are present, the diol has an orientation that is opposite to such groups.