This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition: the formation of all-carbon quaternary centers by reaction with Michael acceptors bearing a polysubstituted unsaturation. Only copper catalysts allow this transformation, along with a careful choice of primary organometallics and chiral ligand. The resulting adducts are useful intermediates for the synthesis of more complex natural products
The copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto polyenic Michael accep...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
L'emploi des ligands de type phosphoramidite pour l'Addition Conjuguée Asymétrique (A.C.A.) catalysé...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
L'emploi des ligands de type phosphoramidite pour l'Addition Conjuguée Asymétrique (A.C.A.) catalysé...
International audienceThe copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto ...
The copper-catalyzed conjugate addition of various Grignard reagents to polyconjugated enones (dieno...
International audienceThe copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto ...
The copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto polyenic Michael accep...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
L'emploi des ligands de type phosphoramidite pour l'Addition Conjuguée Asymétrique (A.C.A.) catalysé...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
L'emploi des ligands de type phosphoramidite pour l'Addition Conjuguée Asymétrique (A.C.A.) catalysé...
International audienceThe copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto ...
The copper-catalyzed conjugate addition of various Grignard reagents to polyconjugated enones (dieno...
International audienceThe copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto ...
The copper-catalyzed asymmetric conjugate addition (ACA) of nucleophiles onto polyenic Michael accep...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...
This thesis documents the development of the copper-catalyzed asymmetric conjugate addition (ACA) of...