Highly enantioselective phase-transfer alkylation of 3-substituted-2-oxindoles with activated bromomethanes is disclosed with a broad substrate scope by using bicyclic guanidinium as a catalyst and a Lewis acid as the co-catalyst. The alkylation adducts are versatile intermediates to accomplish the syntheses of pyrroloindolines and furoindolines
Asymmetric phase-transfer catalysis is a powerful technique that enables a wide range of transformat...
Asymmetric phase-transfer catalysis (PTC) has risen to prominence over the last decade as a straigh...
A new method for a catalytic asymmetric synthesis of $\alpha$-amino acids using phase-transfer catal...
The first strategy for bringing about highly enantioselective alkylative enolate kinetic resolutions...
Catalytic 1,1,3,3-tetramethylguanidine (TMG)-mediated enhancement of enantioselectivity and reactivi...
A cascade reaction that generates pyrrolo- and pyridoindoline motifs from isocyanide precursors unde...
N-Protected oxindole derivatives of unprecedented malleability bearing ester moieties at C-3 have be...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective ...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
The aim of this project is to further develop the application of BSA and its analogues in asymmetric...
A practical synthesis of both enantiomers of unnatural phenylalanine derivatives by using two pseudo...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
The research outlined herein consists of two projects, each relating to the investigation and develo...
2-Acylimidazoles are alkylated under phase-transfer conditions with cinchonidinium catalysts at −40 ...
Asymmetric phase-transfer catalysis is a powerful technique that enables a wide range of transformat...
Asymmetric phase-transfer catalysis (PTC) has risen to prominence over the last decade as a straigh...
A new method for a catalytic asymmetric synthesis of $\alpha$-amino acids using phase-transfer catal...
The first strategy for bringing about highly enantioselective alkylative enolate kinetic resolutions...
Catalytic 1,1,3,3-tetramethylguanidine (TMG)-mediated enhancement of enantioselectivity and reactivi...
A cascade reaction that generates pyrrolo- and pyridoindoline motifs from isocyanide precursors unde...
N-Protected oxindole derivatives of unprecedented malleability bearing ester moieties at C-3 have be...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective ...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
The aim of this project is to further develop the application of BSA and its analogues in asymmetric...
A practical synthesis of both enantiomers of unnatural phenylalanine derivatives by using two pseudo...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
The research outlined herein consists of two projects, each relating to the investigation and develo...
2-Acylimidazoles are alkylated under phase-transfer conditions with cinchonidinium catalysts at −40 ...
Asymmetric phase-transfer catalysis is a powerful technique that enables a wide range of transformat...
Asymmetric phase-transfer catalysis (PTC) has risen to prominence over the last decade as a straigh...
A new method for a catalytic asymmetric synthesis of $\alpha$-amino acids using phase-transfer catal...