By utilising a chiral bicyclic guanidine as catalyst and triethylamine as additive, the first asymmetric Michael addition of α-fluoro-β-ketoesters to various cyclic enones has been successfully developed, affording a variety of Michael adducts with potential synthetic utilities with satisfactory stereoselectivity (up to 94 % ee and 4.3 : 1 dr).Accepted versio
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
Through the Cu-phosphoramidite catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Through the Cu-phosphoramidite catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Through the Cu-phosphoramidite-catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Chiral organofluorine compounds is a rapidly developing area of research because of their importance...
International audienceAn NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
The first example of a photoexcitated amine-catalyzed process for asymmetric Michael addition of <i>...
The asymmetric catalytic synthesis of densely functionalized molecules that contain vicinal quaterna...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
Over the last decade the potential of organocatalysis has successfully been demonstrated. In particu...
A highly stereoselective asymmetric intermolecular conjugate addition of α-amino ester derivatives t...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
Through the Cu-phosphoramidite catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Through the Cu-phosphoramidite catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Through the Cu-phosphoramidite-catalyzed asymmetric conjugate addition a number of chiral cyclic eno...
Chiral organofluorine compounds is a rapidly developing area of research because of their importance...
International audienceAn NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
The first example of a photoexcitated amine-catalyzed process for asymmetric Michael addition of <i>...
The asymmetric catalytic synthesis of densely functionalized molecules that contain vicinal quaterna...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
Over the last decade the potential of organocatalysis has successfully been demonstrated. In particu...
A highly stereoselective asymmetric intermolecular conjugate addition of α-amino ester derivatives t...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...