Although aldol condensation is one of the most important organic reactions, capable of forming new C-C bonds, its mechanism has never been fully established. We now conclude that the rate-limiting step in the base-catalyzed aldol condensation of benzaldehydes with acetophenones, to produce chalcones, is the final loss of hydroxide and formation of the C═C bond. This conclusion is based on a study of the partitioning ratios of the intermediate ketols and on the solvent kinetic isotope effects, whereby the condensations are faster in D2O than in H2O, regardless of substitution
A full mechanistic investigation is proposed for the industrially important cross-aldol condensation...
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes w...
Our previous work demonstrated that hydroxide ion (OH-) was able to catalyze aldol condensation reac...
Although aldol condensation is one of the most important organic reactions, capable of forming new C...
The kinetics of chalcone formation via aldol condensation was studied using UV spectrophotometry. Ch...
Chalcones are a type of molecule that can be considered as easily synthesizable through aldol conden...
The reversible change : acetone diacetone alcohol is studied quantitatively and chemically by using ...
Part I. Intramolecular aldol condensation reactions. The detailed kinetics and equilibrium for the i...
The rate of base-catalysed condensation of acetophenone with substituted benzaldehydes has been stud...
International @ INGENIERIE+FRMInternational audienceThe condensation of ethanol to butanol was inves...
Our previous work demonstrated that hydroxide ion (OH<sup>–</sup>) was able to catalyze aldol conden...
Aldol condensations are one of the most important methods to form carbon-carbon bonds in organic che...
INGENIERIE+FRMThe condensation of ethanol to butanol was investigated over a commercial hydroxyapati...
The efficient conversion of oxygen-rich feedstocks derived from biomass to valuable chemicals and fu...
Aldehydes represent an intermediate redox state of organic carbon and can be precursors to carboxyli...
A full mechanistic investigation is proposed for the industrially important cross-aldol condensation...
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes w...
Our previous work demonstrated that hydroxide ion (OH-) was able to catalyze aldol condensation reac...
Although aldol condensation is one of the most important organic reactions, capable of forming new C...
The kinetics of chalcone formation via aldol condensation was studied using UV spectrophotometry. Ch...
Chalcones are a type of molecule that can be considered as easily synthesizable through aldol conden...
The reversible change : acetone diacetone alcohol is studied quantitatively and chemically by using ...
Part I. Intramolecular aldol condensation reactions. The detailed kinetics and equilibrium for the i...
The rate of base-catalysed condensation of acetophenone with substituted benzaldehydes has been stud...
International @ INGENIERIE+FRMInternational audienceThe condensation of ethanol to butanol was inves...
Our previous work demonstrated that hydroxide ion (OH<sup>–</sup>) was able to catalyze aldol conden...
Aldol condensations are one of the most important methods to form carbon-carbon bonds in organic che...
INGENIERIE+FRMThe condensation of ethanol to butanol was investigated over a commercial hydroxyapati...
The efficient conversion of oxygen-rich feedstocks derived from biomass to valuable chemicals and fu...
Aldehydes represent an intermediate redox state of organic carbon and can be precursors to carboxyli...
A full mechanistic investigation is proposed for the industrially important cross-aldol condensation...
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes w...
Our previous work demonstrated that hydroxide ion (OH-) was able to catalyze aldol condensation reac...