Incorporation of the CF3 group into arenes has found increasing importance in drug discovery. Herein, we report the first photoredox‐catalyzed cross‐coupling of aryl thianthrenium salts with a copper‐based trifluoromethyl reagent, which enables a site‐selective late‐stage trifluoromethylation of arenes. The reaction proceeds with broad functional group tolerance, even for complex small molecules on gram scale. The method was further extended to produce pentafluoroethylated derivatives
Aryl sulfonium salts, in particular aryl thianthrenium salts, have been demonstrated to be valuable ...
This thesis describes a novel method to generate trifluoromethanesulfenyl arene or heteroarene produ...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...
The high abundance of C–H bonds in organic molecules makes C–H functionalization a powerful approach...
With the development of C-H activation reaction in recent several decades, late-stage functionalizat...
Herein, we report a two‐step process forming arene C−O bonds in excellent site‐selectivity at a late...
Trifluoromethyl aryl sulfides (Ar-SCF3) constitute highly attractive building blocks due to their ex...
The conversion of easily available trifluoromethylarenes into aryldifluoromethyl compounds, which ar...
Thianthrenation is a highly selective method to functionalize aromatic C-H-bonds. Electrophilic acti...
Direct C–H functionalization is one of the most straightforward yet challenging strategies to quickl...
A photo-redox-catalyzed procedure for the one-step formation of sultones from alpha,omega-alkenols a...
A photo-redox-catalyzed procedure for the one-step formation of sultones from alpha,omega-alkenols a...
The conversion of easily available trifluoromethylarenes into aryldifluoromethyl compounds, which ar...
The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward ...
Aromatic C–H functionalization, the exchange of hydrogen atoms which are bound to carbon atoms for f...
Aryl sulfonium salts, in particular aryl thianthrenium salts, have been demonstrated to be valuable ...
This thesis describes a novel method to generate trifluoromethanesulfenyl arene or heteroarene produ...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...
The high abundance of C–H bonds in organic molecules makes C–H functionalization a powerful approach...
With the development of C-H activation reaction in recent several decades, late-stage functionalizat...
Herein, we report a two‐step process forming arene C−O bonds in excellent site‐selectivity at a late...
Trifluoromethyl aryl sulfides (Ar-SCF3) constitute highly attractive building blocks due to their ex...
The conversion of easily available trifluoromethylarenes into aryldifluoromethyl compounds, which ar...
Thianthrenation is a highly selective method to functionalize aromatic C-H-bonds. Electrophilic acti...
Direct C–H functionalization is one of the most straightforward yet challenging strategies to quickl...
A photo-redox-catalyzed procedure for the one-step formation of sultones from alpha,omega-alkenols a...
A photo-redox-catalyzed procedure for the one-step formation of sultones from alpha,omega-alkenols a...
The conversion of easily available trifluoromethylarenes into aryldifluoromethyl compounds, which ar...
The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward ...
Aromatic C–H functionalization, the exchange of hydrogen atoms which are bound to carbon atoms for f...
Aryl sulfonium salts, in particular aryl thianthrenium salts, have been demonstrated to be valuable ...
This thesis describes a novel method to generate trifluoromethanesulfenyl arene or heteroarene produ...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...