The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiary and quaternary carbon stereocenters from several synthetic precursors. Despite the utility of these transformations, they have seen little use in the synthesis of natural products. Recently, the power of these reactions was significantly enhanced by the development of enantioselective versions of these transformations. Applications of these methods to the enantioselective syntheses of natural products and pharmaceutical compounds highlight the importance of these developments
Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost reaction has pro...
Zusammenfassung Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost ...
We use first principles quantum mechanics (density functional theory) to report a detailed reaction ...
The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiar...
The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiar...
A highly versatile enantioselective intermolecular Tsuji allylation that generates alpha-quaternary ...
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables t...
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables t...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex na...
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex na...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The enantioselective synthesis of quaternary carbon stereocenters and application to natural product...
Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost reaction has pro...
Zusammenfassung Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost ...
We use first principles quantum mechanics (density functional theory) to report a detailed reaction ...
The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiar...
The family of allylation reactions developed by Tsuji in the 1980s are capable of generating tertiar...
A highly versatile enantioselective intermolecular Tsuji allylation that generates alpha-quaternary ...
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables t...
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables t...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex na...
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex na...
The first catalytic enantioselective examples of the Tsuji allylation using enol carbonates and enol...
The enantioselective synthesis of quaternary carbon stereocenters and application to natural product...
Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost reaction has pro...
Zusammenfassung Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost ...
We use first principles quantum mechanics (density functional theory) to report a detailed reaction ...