A simple and mild procedure to obtain α,β-unsaturated ketones from acetone and a set of benzaldehydes is described. The approach applies bovine serum albumin (BSA) catalysis and water or ethanol, this mild reaction medium contrasting with the strong reaction conditions of the classic aldol condensation. Except for the assayed nitrobenzaldehydes, high enone yields (88?97%) were attained. In addition to its mildness, further advantages of this procedure are the use of a green catalyst exhibiting an efficient reuse and the use of eco-friendly and cheap solvents. In order to gain a deeper understanding of the involved catalytic mechanism, computational experiments on BSA structural analysis and molecular docking were carried out.Fil: Ardanaz, S...
Benzaldehyde lyase from Pseudomonas fluorescens Biovar I. (BAL, EC 4.1.2.38) is a versatile catalyst...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
This Ph.D. thesis deals with the question, if an in situ generation of acetaldehyde is advantageous ...
Bovine serum albumin (BSA) catalyses the cross aldol condensation and proved to be catalytically act...
A variety of unprotected C-glycosidic ketones were employed in a novel enamine-solid-base catalyzed ...
A C-N bond formation reaction under biocompatible conditions for the amination of allenic ketone com...
Here we describe a preliminary investigation on the ability of natural keratin to catalyze the nitro...
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes w...
A current challenge in catalysis is the development of methodologies for the production of bulk chem...
Hydroxy ketones and diols are chiral building blocks of interest in several active pharmaceutical in...
General experimental details All starting materials were obtained commercially from Aldrich, Lancast...
This paper presents a novel, green Knoevenagel procedure for the chemical transformation of benzalde...
Ene reductases catalyze the biocatalytic reduction of activated alkenes, offering a powerful biobase...
Here we describe a preliminary investigation on the ability of natural keratin to catalyze the nitro...
A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemic...
Benzaldehyde lyase from Pseudomonas fluorescens Biovar I. (BAL, EC 4.1.2.38) is a versatile catalyst...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
This Ph.D. thesis deals with the question, if an in situ generation of acetaldehyde is advantageous ...
Bovine serum albumin (BSA) catalyses the cross aldol condensation and proved to be catalytically act...
A variety of unprotected C-glycosidic ketones were employed in a novel enamine-solid-base catalyzed ...
A C-N bond formation reaction under biocompatible conditions for the amination of allenic ketone com...
Here we describe a preliminary investigation on the ability of natural keratin to catalyze the nitro...
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes w...
A current challenge in catalysis is the development of methodologies for the production of bulk chem...
Hydroxy ketones and diols are chiral building blocks of interest in several active pharmaceutical in...
General experimental details All starting materials were obtained commercially from Aldrich, Lancast...
This paper presents a novel, green Knoevenagel procedure for the chemical transformation of benzalde...
Ene reductases catalyze the biocatalytic reduction of activated alkenes, offering a powerful biobase...
Here we describe a preliminary investigation on the ability of natural keratin to catalyze the nitro...
A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemic...
Benzaldehyde lyase from Pseudomonas fluorescens Biovar I. (BAL, EC 4.1.2.38) is a versatile catalyst...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
This Ph.D. thesis deals with the question, if an in situ generation of acetaldehyde is advantageous ...