The relative rates of the aldol reaction catalyzed by supported primary and secondary amines can be inverted by 2 orders of magnitude, depending on the use of hexane or water as a solvent. Our analyses suggest that this dramatic shift in the catalytic behavior of the supported amines does not involve differences in reaction mechanism, but is caused by activation of imine to enamine equilibria and stabilization of iminium species. The effects of solvent polarity and acidity were found to be important to the performance of the catalytic reaction. This study highlights the critical role of solvent in multicomponent heterogeneous catalytic processes
Chemo- and regioselectivity in a heterogeneously catalyzed cross aldol reaction were directed by tun...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...
The reusability of methylaminopropyl active sites grafted on mesoporous amorphous silica, either wit...
tAminated silica materials are known to efficiently catalyse aldol condensations, especially when si...
Intramolecular cooperativity in heterogeneous organocatalysts is investigated using alkanolamine-fun...
In this study, we demonstrate how materials science can be combined with the established methods of ...
The Michael addition of nitromethane to cinnamaldehyde has been computationally studied in the absen...
Despite intense interest in amine-catalyzed stereoselective reactions, high catalyst loadings of ≥10...
During the past two decades, new insights have driven the development and optimization of aminated m...
The effect of protic solvents on the rate and stereochemical outcome of the imidazolidinone-catalyze...
Aldol condensation is an important C-C bond formation reaction in chemical synthesis that finds vers...
The Hayashi–Ito aldol reaction of methyl isocyanoacetate (MI) and benzaldehydes, a classic homogeneo...
The experimentally observed effects of water, and the effects of silanol groups, on the liquid-phase...
The aldol reaction catalyzed by an amine-substituted mesoporous silica nanoparticle (amine-MSN) surf...
Chemo- and regioselectivity in a heterogeneously catalyzed cross aldol reaction were directed by tun...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...
The reusability of methylaminopropyl active sites grafted on mesoporous amorphous silica, either wit...
tAminated silica materials are known to efficiently catalyse aldol condensations, especially when si...
Intramolecular cooperativity in heterogeneous organocatalysts is investigated using alkanolamine-fun...
In this study, we demonstrate how materials science can be combined with the established methods of ...
The Michael addition of nitromethane to cinnamaldehyde has been computationally studied in the absen...
Despite intense interest in amine-catalyzed stereoselective reactions, high catalyst loadings of ≥10...
During the past two decades, new insights have driven the development and optimization of aminated m...
The effect of protic solvents on the rate and stereochemical outcome of the imidazolidinone-catalyze...
Aldol condensation is an important C-C bond formation reaction in chemical synthesis that finds vers...
The Hayashi–Ito aldol reaction of methyl isocyanoacetate (MI) and benzaldehydes, a classic homogeneo...
The experimentally observed effects of water, and the effects of silanol groups, on the liquid-phase...
The aldol reaction catalyzed by an amine-substituted mesoporous silica nanoparticle (amine-MSN) surf...
Chemo- and regioselectivity in a heterogeneously catalyzed cross aldol reaction were directed by tun...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...
Aminopropyl-functionalized mesoporous silica nanoparticles (AP-MSN) catalyze aldol condensations. Th...