A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-butyl isocyanide as “CN” source, which provides a new and unique strategy for the preparation of (hetero)aryl nitriles. Indoles, pyrroles, and aromatic rings could be efficiently cyanated through C–H bond activation with high regioselectivity
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
Playing it safe: The nontoxic cyanide source K[subscript 4][Fe(CN)[subscript 6]⋅3 H[subscript 2]O ca...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
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...
A palladium-catalyzed cyanation of aryl halides with hexamethylenetetramine as a safe cyanide source...
cross-coupling; heterocycles; homogeneous catalysis; palladium; cyanides Aromatic nitriles have appl...
Transition-metal-catalyzed cyanation of aryl halides is a process of significant importance in the p...
This paper describes the direct cyanation of indoles and benzofurans employing N,N-dimethylformamide...
A palladium-catalyzed cyanation of alkenyl halides using acetone cyanohydrin is described. A number ...
A palladium-catalyzed cyanation of alkenyl halides using acetone cyanohydrin is described. A number ...
An unprecedented palladium-catalyzed cyanation of aromatic C–H bonds by using tertiary amine derived...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
BF3·OEt2 catalyzed 1,6-conjugate addition of tert-butyl isocyanide to para-quinone methides and fuch...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
Playing it safe: The nontoxic cyanide source K[subscript 4][Fe(CN)[subscript 6]⋅3 H[subscript 2]O ca...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
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...
A palladium-catalyzed cyanation of aryl halides with hexamethylenetetramine as a safe cyanide source...
cross-coupling; heterocycles; homogeneous catalysis; palladium; cyanides Aromatic nitriles have appl...
Transition-metal-catalyzed cyanation of aryl halides is a process of significant importance in the p...
This paper describes the direct cyanation of indoles and benzofurans employing N,N-dimethylformamide...
A palladium-catalyzed cyanation of alkenyl halides using acetone cyanohydrin is described. A number ...
A palladium-catalyzed cyanation of alkenyl halides using acetone cyanohydrin is described. A number ...
An unprecedented palladium-catalyzed cyanation of aromatic C–H bonds by using tertiary amine derived...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
BF3·OEt2 catalyzed 1,6-conjugate addition of tert-butyl isocyanide to para-quinone methides and fuch...
Methods for the direct C–H functionalization of aromatic compounds are in demand for a variety of ap...
Playing it safe: The nontoxic cyanide source K[subscript 4][Fe(CN)[subscript 6]⋅3 H[subscript 2]O ca...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...