52239-32-4

Upstream product

• 625-48-9 2-nitro-1-ethanol 
• 100-52-7 benzaldehyde 
• 96040-15-2 2-(3-phenyl-2-nitro3-hydroxy-propanoxy) tetrahydro-pyran 

Downstream Products

• 77834-98-1 threo-1-phenyl-2-nitro-1,3-propanediol bis(p-chlorobenzoate) 
• 3306-06-7 1R,2S(+)-2-amino-1-phenyl-1,3-propanediol 

Relevant academic research and scientific papers

Quantitative Evaluation of the Catalytic Activity of Dendrimers with only One Active Center at the Core: Application to the Nitroaldol (Henry) Reaction

One reference tertiary amine and three families of structurally related trialkylamines and dendrimers have been synthesized, characterized, and studied by molecular dynamics simulations. The catalytic activity of these amines in the nitroaldol (Henry) reaction between 2-nitroethanol and benzaldehyde has been measured by FT-IR spectroscopy. It is found that, in this kind of molecule with only one catalytic center at the core, the efficiency of the catalytic process decreases with the size and/or the degree of ramification of the dendrimer. According to these results, there is a linear departure from the behavior predicted by the hard sphere collision theory (HSCT) as the size of the dendrimer increases. Therefore, the behavior of structurally related dendrimers can be quantified in terms of their molecular weight and reagent accessible surfaces.

Dendritic catalysts for the nitroaldol (Henry) reaction

Dendritic molecules with a single triethylene amine core surrounded by hyperbranched polyether sectors catalyze the nitroaldol reaction between aromatic aldehydes and nitroalkanes.

Addition of aldehydes to organic compounds having a carbon-hydrogen bond activated by a nitro or nitrile group

Low valent transition metal complexes containing small cone angle phosphine or arsine ligands efficiently catalyze addition of aldehydes to compounds or groups having a C--H bond activated by a nitro or nitrile group, to provide nitroalcohols or cyanohydrins, respectively.