The application of chiral sulfinamides and achiral sulfonic acids as a co-catalyst system for enantioselective protonation reactions is described. Structurally simple, easily accessible sulfinamides were found to induce moderate-to-high eeʼs in the formation of 2-aryl-substituted cycloalkanones from the corresponding trimethylsilyl enol ethers.Chemistry and Chemical Biolog
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselec...
Enantioselective protonation is conceptually one of the most attractive methods to generate an α-chi...
A general study of the enantioselective protonation of prochiral enolates with 2-sulfinyl alcohols i...
The development of new catalysts for asymmetric organic transformations is a broad and important res...
The activation of olefins for asymmetric chemical synthesis traditionally relies on transition metal...
We report the design and synthesis of a strong, chiral, enantiopure sulfoxide-based C–H acid. Single...
Cinchona alkaloid-derived organocatalysts are widely employed in various asymmetric transformations,...
AbstractTwo new families of chiral arenesulfonic acids were synthesised in a short, robust and scala...
We report a highly enantioselective catalytic protonation of bis‐silyl ketene acetals. Our method de...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
Although anion-binding processes are well-known for their crucial role in molecular recognition, the...
An efficient chiral Brønsted acid-catalyzed enantioselective dehydrative Nazarov-type electrocycliza...
The authors thank the Leverhulme Trust for funding (C.X.; RPG-2015- 308) and GSK for a PhD studentsh...
Enantioselective protonation is a common process in biosynthetic sequences. The decarboxylase and es...
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselec...
Enantioselective protonation is conceptually one of the most attractive methods to generate an α-chi...
A general study of the enantioselective protonation of prochiral enolates with 2-sulfinyl alcohols i...
The development of new catalysts for asymmetric organic transformations is a broad and important res...
The activation of olefins for asymmetric chemical synthesis traditionally relies on transition metal...
We report the design and synthesis of a strong, chiral, enantiopure sulfoxide-based C–H acid. Single...
Cinchona alkaloid-derived organocatalysts are widely employed in various asymmetric transformations,...
AbstractTwo new families of chiral arenesulfonic acids were synthesised in a short, robust and scala...
We report a highly enantioselective catalytic protonation of bis‐silyl ketene acetals. Our method de...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
Although anion-binding processes are well-known for their crucial role in molecular recognition, the...
An efficient chiral Brønsted acid-catalyzed enantioselective dehydrative Nazarov-type electrocycliza...
The authors thank the Leverhulme Trust for funding (C.X.; RPG-2015- 308) and GSK for a PhD studentsh...
Enantioselective protonation is a common process in biosynthetic sequences. The decarboxylase and es...
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselec...
Enantioselective protonation is conceptually one of the most attractive methods to generate an α-chi...