The excited radical anion of rhodamine 6G reduces heteroaryl bromides and chlorides to generate heteroaryl radicals that were successively trapped by pyrroles for the synthesis of heteroaromatic biaryls in moderate to excellent yields. The synthetically important photoredox catalytic C-H heteroarylation reaction works for a broad range of brominated electron-rich heteroarenes and chlorinated heteroarenes bearing electron withdrawing groups. In addition, this methodology was applied to the formal synthesis of a benzimidazole derivative II with interesting pharmacological properties
The 2-azolyl radical, generated from 2-bromoazoles via photocatalysis, is a powerful intermediate fo...
We report the development of a method for room-temperature C–H hydroxymethylation of heteroarenes. A...
C–H functionalization of electron-deficient heteroarenes using commercial unactivated alkyl halides ...
Substituted heterocycles are common building-blocks for biologically relevant molecules and represen...
In the heterobiaryl cross-coupling reaction between aryl halides (Ar-X) and N-methylpyrrole (N-MP) c...
International audienceBenzoyl azides were used for the direct and atom economic C-H amidation of ele...
Aryl–aryl cross-coupling constitutes one of the most widely used procedures for the synthesis of hig...
Arylated nucleobases were synthesized by visible light photocatalysis using rhodamine 6G as photored...
Although transition-metal-catalyzed direct arylation of aromatic C–H bonds is one of the most effici...
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built around the ...
Aromatic heterocycles are omnipresent structural motifs in various natural products, pharmaceuticals...
A photochemical cross-coupling protocol towards bi(hetero)aryls has been developed. The coupling rea...
A photochemical cross-coupling protocol towards bi(hetero)aryls has been developed. The coupling rea...
The tricyclic aromatic ketone 9-anthrone and its derivatives are under basic conditions in equilibri...
The tricyclic aromatic ketone 9-anthrone and its derivatives are under basic conditions in equilibri...
The 2-azolyl radical, generated from 2-bromoazoles via photocatalysis, is a powerful intermediate fo...
We report the development of a method for room-temperature C–H hydroxymethylation of heteroarenes. A...
C–H functionalization of electron-deficient heteroarenes using commercial unactivated alkyl halides ...
Substituted heterocycles are common building-blocks for biologically relevant molecules and represen...
In the heterobiaryl cross-coupling reaction between aryl halides (Ar-X) and N-methylpyrrole (N-MP) c...
International audienceBenzoyl azides were used for the direct and atom economic C-H amidation of ele...
Aryl–aryl cross-coupling constitutes one of the most widely used procedures for the synthesis of hig...
Arylated nucleobases were synthesized by visible light photocatalysis using rhodamine 6G as photored...
Although transition-metal-catalyzed direct arylation of aromatic C–H bonds is one of the most effici...
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built around the ...
Aromatic heterocycles are omnipresent structural motifs in various natural products, pharmaceuticals...
A photochemical cross-coupling protocol towards bi(hetero)aryls has been developed. The coupling rea...
A photochemical cross-coupling protocol towards bi(hetero)aryls has been developed. The coupling rea...
The tricyclic aromatic ketone 9-anthrone and its derivatives are under basic conditions in equilibri...
The tricyclic aromatic ketone 9-anthrone and its derivatives are under basic conditions in equilibri...
The 2-azolyl radical, generated from 2-bromoazoles via photocatalysis, is a powerful intermediate fo...
We report the development of a method for room-temperature C–H hydroxymethylation of heteroarenes. A...
C–H functionalization of electron-deficient heteroarenes using commercial unactivated alkyl halides ...