A protected pyruvate equivalent is described that allows arylation and arylation/alkylation reactions to be performed at the methyl group. Utilization of the OBO derivative of the pyruvate ester allowed the application of palladium catalyzed arylation reactions together with subsequent alkylation, under basic conditions. Moreover, the OBO protecting group could be easily removed in one step to provide access to a wide range of substituted pyruvate derivatives
The zirconocene-catalyzed rearrangement of epoxy esters to give 2,7,8-trioxabicyclo[3.2.1]octanes (A...
Alkoxycarbonylation of arylsulfoniums has been developed with the aid of a catalytic amount of a pal...
We report the development of a procedure for the ??-arylation of esters on 42 mmol scale which did n...
Chapter 1. Introduction A literature background on the early development of the Pd-catalysed cross-c...
Eater enolates are generated by reductive α-deacetoxylation of α-acetoxy-α-arylmaloni...
The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc ...
A mild and efficient one-pot synthesis of esters based on the Pd-catalyzed alkoxy- and aryloxycarbon...
The palladium-catalyzed R-arylation of ketones has become a useful and general synthetic method. In ...
Abstract: The zirconocene-catalyzed rearrangement of epoxy esters to give 2,7,8-trioxabicy-clo[3.2.1...
Palladium-catalyzed alkoxycarbonylation of the C≡C triple bond of propargyl alcohol is a sustainable...
Enolate alkylation, the nucleophilic substitution of electrophilic alkylating reagents by carbon nuc...
With alkyl carbazates as the green ester source, a novel palladium-catalyzed oxidative free radical ...
The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc ...
The palladium-catalyzed coupling of an enolate with an ortho-functionalized aryl halide (an α-arylat...
International audienceHeteroaromatics bearing unprotected hydroxyalkyl functions can be arylated usi...
The zirconocene-catalyzed rearrangement of epoxy esters to give 2,7,8-trioxabicyclo[3.2.1]octanes (A...
Alkoxycarbonylation of arylsulfoniums has been developed with the aid of a catalytic amount of a pal...
We report the development of a procedure for the ??-arylation of esters on 42 mmol scale which did n...
Chapter 1. Introduction A literature background on the early development of the Pd-catalysed cross-c...
Eater enolates are generated by reductive α-deacetoxylation of α-acetoxy-α-arylmaloni...
The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc ...
A mild and efficient one-pot synthesis of esters based on the Pd-catalyzed alkoxy- and aryloxycarbon...
The palladium-catalyzed R-arylation of ketones has become a useful and general synthetic method. In ...
Abstract: The zirconocene-catalyzed rearrangement of epoxy esters to give 2,7,8-trioxabicy-clo[3.2.1...
Palladium-catalyzed alkoxycarbonylation of the C≡C triple bond of propargyl alcohol is a sustainable...
Enolate alkylation, the nucleophilic substitution of electrophilic alkylating reagents by carbon nuc...
With alkyl carbazates as the green ester source, a novel palladium-catalyzed oxidative free radical ...
The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc ...
The palladium-catalyzed coupling of an enolate with an ortho-functionalized aryl halide (an α-arylat...
International audienceHeteroaromatics bearing unprotected hydroxyalkyl functions can be arylated usi...
The zirconocene-catalyzed rearrangement of epoxy esters to give 2,7,8-trioxabicyclo[3.2.1]octanes (A...
Alkoxycarbonylation of arylsulfoniums has been developed with the aid of a catalytic amount of a pal...
We report the development of a procedure for the ??-arylation of esters on 42 mmol scale which did n...