Novel enamine–metal Lewis acid bifunctional catalysts were successfully applied to the asymmetric Michael addition of ketones to alkylidene malonates, offering excellent stereoselectivity (up to >99% <i>ee</i> and >99:1 <i>dr</i>). The asymmetric Michael addition of ketones to allylidene malonates was also achieved
The Michael reaction of a dialkyl malonate with a cyclic enone using a chiral diamine-acid combinati...
The highly enantioselective Michael addition of malonates to alpha,beta-unsaturated ketones in water...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
Novel enamine–metal Lewis acid bifunctional catalysts were successfully applied to the asymmetric Mi...
Abstract: The Michael additions of a number of ketones and alde-hydes to alkylidene malonates and ni...
An open–close strategy in asymmetric catalysis is newly developed. With this powerful strategy, lact...
Cinchona alkaloid derived primary amine thioureas organo catalyzed Michael addition of nitroalkanes ...
The efficient asymmetric Michael addition reactions of aryl methyl ketones with 2-furanones were cat...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
A diastereodivergent catalytic asymmetric Michael addition of 2-oxindoles to α,β-unsaturated ketones...
Lewis base-Bronsted base bifunctional catalysis is a novel and practical strategy for the asymmetric...
A heterobimetallic catalyst obtained by reaction of LiAlH<SUB>4</SUB> with aminodiol derived from na...
Organocatalytic asymmetric reactions have proved to be efficient and powerful tools in organic synth...
Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by an as...
Alkali metal salts of substituted (S)-prolines, alkali metal alkoxides of (S)-prolinol, and Na salts...
The Michael reaction of a dialkyl malonate with a cyclic enone using a chiral diamine-acid combinati...
The highly enantioselective Michael addition of malonates to alpha,beta-unsaturated ketones in water...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
Novel enamine–metal Lewis acid bifunctional catalysts were successfully applied to the asymmetric Mi...
Abstract: The Michael additions of a number of ketones and alde-hydes to alkylidene malonates and ni...
An open–close strategy in asymmetric catalysis is newly developed. With this powerful strategy, lact...
Cinchona alkaloid derived primary amine thioureas organo catalyzed Michael addition of nitroalkanes ...
The efficient asymmetric Michael addition reactions of aryl methyl ketones with 2-furanones were cat...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
A diastereodivergent catalytic asymmetric Michael addition of 2-oxindoles to α,β-unsaturated ketones...
Lewis base-Bronsted base bifunctional catalysis is a novel and practical strategy for the asymmetric...
A heterobimetallic catalyst obtained by reaction of LiAlH<SUB>4</SUB> with aminodiol derived from na...
Organocatalytic asymmetric reactions have proved to be efficient and powerful tools in organic synth...
Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by an as...
Alkali metal salts of substituted (S)-prolines, alkali metal alkoxides of (S)-prolinol, and Na salts...
The Michael reaction of a dialkyl malonate with a cyclic enone using a chiral diamine-acid combinati...
The highly enantioselective Michael addition of malonates to alpha,beta-unsaturated ketones in water...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...