The proline-catalyzed asymmetric aldol reaction between aliphatic aldehydes and acetone has, to date, remained underdeveloped. Challenges in controlling this reaction include avoiding undesired side reactions such as aldol condensation and self-aldolization. In recent years we have developed optimized conditions, which enable high yields and good to excellent enantioselectivities, and which are presented in this communication
ABSTRACT. A series of chiral prolinamide compounds with pyridine-2, 6-dicarboxylic acid moieties der...
The proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar aprotic sol...
Most enzymatic transformations have a synthetic counterpart. Often though, the mechanisms by which n...
The proline-catalyzed asymmetric aldol reaction between aliphatic aldehydes and acetone has, to date...
L-Proline-catalysed direct asymmetric aldol reaction of acetone with various aldehydes in PEG-400 is...
L-Prolinamides 2, prepared from L-proline and simple aliphatic and aromatic amines, have been found ...
With this communication we extend the methodology of proline-catalyzed direct asymmetric aldol react...
L-Prolinamides 2, prepared from L-proline and simple aliphatic and aromatic amines, have been found ...
A rapid L-proline catalyzed direct aldol reaction between various aldehydes and acetone was achieved...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
An intriguing effect of electronegative 2,6-substituents on the stereochemical outcome of (S)-prolin...
The synthesis of multifunctional organic catalysts, easily obtained by the condensation of (S)-proli...
ABSTRACT. A series of chiral prolinamide compounds with pyridine-2, 6-dicarboxylic acid moieties der...
The proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar aprotic sol...
Most enzymatic transformations have a synthetic counterpart. Often though, the mechanisms by which n...
The proline-catalyzed asymmetric aldol reaction between aliphatic aldehydes and acetone has, to date...
L-Proline-catalysed direct asymmetric aldol reaction of acetone with various aldehydes in PEG-400 is...
L-Prolinamides 2, prepared from L-proline and simple aliphatic and aromatic amines, have been found ...
With this communication we extend the methodology of proline-catalyzed direct asymmetric aldol react...
L-Prolinamides 2, prepared from L-proline and simple aliphatic and aromatic amines, have been found ...
A rapid L-proline catalyzed direct aldol reaction between various aldehydes and acetone was achieved...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
Synthesis and successful applications in terms of chemical yields and diastereo-/enantiomeric ratios...
An intriguing effect of electronegative 2,6-substituents on the stereochemical outcome of (S)-prolin...
The synthesis of multifunctional organic catalysts, easily obtained by the condensation of (S)-proli...
ABSTRACT. A series of chiral prolinamide compounds with pyridine-2, 6-dicarboxylic acid moieties der...
The proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar aprotic sol...
Most enzymatic transformations have a synthetic counterpart. Often though, the mechanisms by which n...