New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in hand, the development of further transformations allowed for the synthesis of diverse derivatives of high pharmaceutical value, such as the Belliotti (S)-PD172938 and arylated analogues with hypnotic sedative activity, obtained in good overall total yield (50%) and high enantiomeric purity (95% ee). The synthetic routes developed herein are particularly convenient in comparison with the current methods available in literature and are particularly promising for large scale applications
Abstract: Activated 3-substituted isoindolinones have been investigated as nucleophiles in the organ...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
The tuning of aldol/cyclization cascade reactions of glycine Schiff bases with 2-cyano benzaldehydes...
New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective ...
In this work we report our endeavors toward the development of an asymmetric synthesis of a 3,3-disu...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
In this work, we investigated two strategies for the synthesis of the challenging ketones 2-acylbenz...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
International audienceA new asymmetric organocatalyzed intramolecular aza-Michael reaction under a d...
In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substitute...
The research outlined herein consists of two projects, each relating to the investigation and develo...
Abstract: Activated 3-substituted isoindolinones have been investigated as nucleophiles in the organ...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
The tuning of aldol/cyclization cascade reactions of glycine Schiff bases with 2-cyano benzaldehydes...
New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective ...
In this work we report our endeavors toward the development of an asymmetric synthesis of a 3,3-disu...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
In this work, we investigated two strategies for the synthesis of the challenging ketones 2-acylbenz...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
International audienceA new asymmetric organocatalyzed intramolecular aza-Michael reaction under a d...
In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substitute...
The research outlined herein consists of two projects, each relating to the investigation and develo...
Abstract: Activated 3-substituted isoindolinones have been investigated as nucleophiles in the organ...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
The tuning of aldol/cyclization cascade reactions of glycine Schiff bases with 2-cyano benzaldehydes...