A cobalt-catalyzed C–H cyanation reaction of arenes has been developed using <i>N</i>-cyanosuccinimide as a new electrophilic cyanating agent. The reaction proceeds with high selectivity to afford monocyanated products with excellent functional group tolerance. Substrate scope was found to be broad enough to include a wide range of heterocycles including 6-arylpurines
Aromatic nitriles are key structural units in organic chemistry and, therefore, highly attractive ta...
cross-coupling; heterocycles; homogeneous catalysis; palladium; cyanides Aromatic nitriles have appl...
This research project led to the development of new coupling reactions catalysed b...
A cobalt-catalyzed C–H cyanation reaction of arenes has been developed using <i>N</i>-cyanosuccinimi...
A cobalt-catalyzed C−H cyanation reaction of arenes has been developed using N-cyanosuccinimide as a...
The first cobalt-catalyzed cyanation, halogenation, and allylation via C–H activation have been real...
The Co(III)-catalyzed direct C–H amidation of arenes has been developed using <i>O</i>-acylcarbamat...
We describe herein a novel synthesis of various homoallylic nitriles via cobalt-catalyzed hydrocyana...
A cationic cobalt(III)-catalyzed direct CH amidation of unactivated (hetero)arenes and alkenes by us...
Aromatic nitriles are key structural units in organic chemistry and thus highly attractive targets f...
An easily removable pyrimidine-based auxiliary has been employed for the remote meta-C-H cyanation o...
The Co(III)-catalyzed direct C−H amidation of arenes has been developed using O-acylcarbamates as a ...
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...
This research project led to the development of new coupling reactions catalysed b...
Aromatic nitriles are key structural units in organic chemistry and, therefore, highly attractive ta...
cross-coupling; heterocycles; homogeneous catalysis; palladium; cyanides Aromatic nitriles have appl...
This research project led to the development of new coupling reactions catalysed b...
A cobalt-catalyzed C–H cyanation reaction of arenes has been developed using <i>N</i>-cyanosuccinimi...
A cobalt-catalyzed C−H cyanation reaction of arenes has been developed using N-cyanosuccinimide as a...
The first cobalt-catalyzed cyanation, halogenation, and allylation via C–H activation have been real...
The Co(III)-catalyzed direct C–H amidation of arenes has been developed using <i>O</i>-acylcarbamat...
We describe herein a novel synthesis of various homoallylic nitriles via cobalt-catalyzed hydrocyana...
A cationic cobalt(III)-catalyzed direct CH amidation of unactivated (hetero)arenes and alkenes by us...
Aromatic nitriles are key structural units in organic chemistry and thus highly attractive targets f...
An easily removable pyrimidine-based auxiliary has been employed for the remote meta-C-H cyanation o...
The Co(III)-catalyzed direct C−H amidation of arenes has been developed using O-acylcarbamates as a ...
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...
This research project led to the development of new coupling reactions catalysed b...
Aromatic nitriles are key structural units in organic chemistry and, therefore, highly attractive ta...
cross-coupling; heterocycles; homogeneous catalysis; palladium; cyanides Aromatic nitriles have appl...
This research project led to the development of new coupling reactions catalysed b...