Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of applications, including the synthesis of agrochemicals, pharmaceuticals, and materials. Herein, we disclose the construction of aromatic nitriles via direct C–H functionalization using an acridinium photoredox catalyst and trimethylsilyl cyanide under an aerobic atmosphere. The reaction proceeds at room temperature under mild conditions and has proven to be compatible with a variety of electron-donating and -withdrawing groups, halogens, and nitrogen- and oxygen-containing heterocycles, as well as aromatic-containing pharmaceutical agents
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
A palladium-catalyzed cyanation of aryl halides with hexamethylenetetramine as a safe cyanide source...
A novel approach to the Cu-catalyzed cyanation of simple arenes using acetonitrile as an attractive ...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
A Rh-catalyzed directed C–H cyanation reaction was developed for the first time as a practical metho...
A Rh-catalyzed directed C–H cyanation reaction was developed for the first time as a practical metho...
Aromatic nitriles are key structural units in organic chemistry and thus highly attractive targets f...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
An efficient rhodium-catalyzed regioselective C–H bond cyanation of arenes was developed using <i>te...
An efficient rhodium-catalyzed regioselective C–H bond cyanation of arenes was developed using <i>te...
Nitriles are recurring motifs in bioactive molecules and versatile functional groups in synthetic ch...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
A palladium-catalyzed cyanation of aryl halides with hexamethylenetetramine as a safe cyanide source...
A novel approach to the Cu-catalyzed cyanation of simple arenes using acetonitrile as an attractive ...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
A Rh-catalyzed directed C–H cyanation reaction was developed for the first time as a practical metho...
A Rh-catalyzed directed C–H cyanation reaction was developed for the first time as a practical metho...
Aromatic nitriles are key structural units in organic chemistry and thus highly attractive targets f...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
An efficient rhodium-catalyzed regioselective C–H bond cyanation of arenes was developed using <i>te...
An efficient rhodium-catalyzed regioselective C–H bond cyanation of arenes was developed using <i>te...
Nitriles are recurring motifs in bioactive molecules and versatile functional groups in synthetic ch...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
A palladium-catalyzed cyanation of aryl halides with hexamethylenetetramine as a safe cyanide source...
A novel approach to the Cu-catalyzed cyanation of simple arenes using acetonitrile as an attractive ...