International audienceThe palladium‐catalyzed decarboxylative asymmetric protonation (DAP) of racemic allyl β‐keto esters using achiral protic species, first disclosed in 2006, is now a mature methodology for applications in asymmetric organic synthesis. In contrast, the mechanism of protonation remains unclear despite experimental and computational studies. The aim of this review is, firstly, to gather together the literature results, observations and proposals and, secondly, to suggest, for the enantioselectivity‐determining step, transition states depending on the substrate and the proton source
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of alpha-amino mal...
Dissertation (Ph.D.)--University of Kansas, Chemistry, 2007.The generation, and subsequent allylatio...
The reaction mechanism and the origins of regio- and enantioselectivities for Pd-catalyzed asymmetri...
Herein, we describe a study into the scope and origin of an enantiodivergent effect in the palladium...
General homogeneous conditions for the palladium-catalyzed synthesis of carbonyl compounds with tert...
Chiral molecules exist in two different forms called enantiomers, which are non-superimposable mirro...
A palladium-catalyzed decarboxylative asymmetric allylic alkylation (Pd-DAAA) of benzo-fused and non...
This account describes the circumstances leading to our group's innovations in the area of decarbox...
We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary s...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of α-amino malonat...
The density functional (M06) computations on a cooperative multicatalytic reaction involving palladi...
The density functional (M06) computations on a cooperative multicatalytic reaction involving palladi...
The first method for the asymmetric synthesis of C3-monosubstituted chiral carbazolones, structural ...
The Pd-catalyzed decarboxylative asymmetric allylic alkylation of enolate nucleophiles is a cornerst...
Dicationic palladium(II) complexes have been shown to catalyse a number of important asymmetric tran...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of alpha-amino mal...
Dissertation (Ph.D.)--University of Kansas, Chemistry, 2007.The generation, and subsequent allylatio...
The reaction mechanism and the origins of regio- and enantioselectivities for Pd-catalyzed asymmetri...
Herein, we describe a study into the scope and origin of an enantiodivergent effect in the palladium...
General homogeneous conditions for the palladium-catalyzed synthesis of carbonyl compounds with tert...
Chiral molecules exist in two different forms called enantiomers, which are non-superimposable mirro...
A palladium-catalyzed decarboxylative asymmetric allylic alkylation (Pd-DAAA) of benzo-fused and non...
This account describes the circumstances leading to our group's innovations in the area of decarbox...
We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary s...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of α-amino malonat...
The density functional (M06) computations on a cooperative multicatalytic reaction involving palladi...
The density functional (M06) computations on a cooperative multicatalytic reaction involving palladi...
The first method for the asymmetric synthesis of C3-monosubstituted chiral carbazolones, structural ...
The Pd-catalyzed decarboxylative asymmetric allylic alkylation of enolate nucleophiles is a cornerst...
Dicationic palladium(II) complexes have been shown to catalyse a number of important asymmetric tran...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of alpha-amino mal...
Dissertation (Ph.D.)--University of Kansas, Chemistry, 2007.The generation, and subsequent allylatio...
The reaction mechanism and the origins of regio- and enantioselectivities for Pd-catalyzed asymmetri...