Asymmetric functionalization of alkylacetic esters and their derivatives is traditionally achieved via preformed enolates with chiral auxiliaries. Catalytic versions of such transformations are attractive but challenging. A direct catalytic activation of simple alkylacetic esters via N-heterocyclic carbene organocatalysts to generate chiral enolate intermediates for highly enantioselective reactions is reported
This thesis focuses on esters activation and desymmetrization for enantioselective reactions enabled...
The direct γ-carbon functionalization of α,β-unsaturated esters <i>via N</i>-Heterocyclic Carbene (N...
route to enantioenriched α-amino esters by direct reaction of α-chloroglycine ester as a practical i...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
The activation of the α-carbons of carboxylic esters and related carbonyl compounds to generate enol...
An NHC-catalyzed activation of acetic esters to afford enolate intermediates is disclosed. The catal...
An NHC-catalyzed activation of acetic esters to afford enolate intermediates is disclosed. The catal...
International audienceA focused library of chiral imidazolinium salts functionalized with urea-type ...
Carboxylic esters can be readily obtained at low cost. Therefore, asymmetric catalytic activation of...
A convergent, organocatalytic asymmetric aminomethylation of α,β-unsaturated aldehydes by N-heterocy...
An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkyl...
The direct γ-carbon functionalization of α,β-unsaturated esters via N-Heterocyclic Carbene (NHC) cat...
This thesis describes studies on non-classical carbocations and enols in asymmetric catalysis. In th...
Since the first enantioselective carbon-carbon bond formations catalyzed by N-heterocyclic carbenes ...
This thesis focuses on esters activation and desymmetrization for enantioselective reactions enabled...
The direct γ-carbon functionalization of α,β-unsaturated esters <i>via N</i>-Heterocyclic Carbene (N...
route to enantioenriched α-amino esters by direct reaction of α-chloroglycine ester as a practical i...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
The activation of the α-carbons of carboxylic esters and related carbonyl compounds to generate enol...
An NHC-catalyzed activation of acetic esters to afford enolate intermediates is disclosed. The catal...
An NHC-catalyzed activation of acetic esters to afford enolate intermediates is disclosed. The catal...
International audienceA focused library of chiral imidazolinium salts functionalized with urea-type ...
Carboxylic esters can be readily obtained at low cost. Therefore, asymmetric catalytic activation of...
A convergent, organocatalytic asymmetric aminomethylation of α,β-unsaturated aldehydes by N-heterocy...
An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkyl...
The direct γ-carbon functionalization of α,β-unsaturated esters via N-Heterocyclic Carbene (NHC) cat...
This thesis describes studies on non-classical carbocations and enols in asymmetric catalysis. In th...
Since the first enantioselective carbon-carbon bond formations catalyzed by N-heterocyclic carbenes ...
This thesis focuses on esters activation and desymmetrization for enantioselective reactions enabled...
The direct γ-carbon functionalization of α,β-unsaturated esters <i>via N</i>-Heterocyclic Carbene (N...
route to enantioenriched α-amino esters by direct reaction of α-chloroglycine ester as a practical i...