A Cu-diamine complex effectively catalyses tandem C-N bond formation on 2-(2-haloalkenyl)-aryl halide substrates, to deliver a series of N-functionalised indoles. Anilines, amides and carbamates are all effective coupling partners under the developed conditions
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
DMPAO has been found to be a powerful ligand to enable copper-catalyzed coupling of aryl halides wit...
<i>N</i>-Substituted indoles are synthesized from primary amines through a tandem reaction sequence....
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C–N bon...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
A copper-catalyzed intramolecular amidation of unactivated C(sp(3))-H bonds to construct indoline de...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
The Larsen group specializes in maximizing the potential of simple organic substrates through single...
Indole-carboxylates are N-arylated with 2-bromopyridines using stoichiometric copper(II) oxide/potas...
International audienceA mini-review describes the development of the catalysis by Cu(I) complexes ai...
A versatile protocol for the C–H chalcogenation of indolines and indoles by means of copper catalysi...
The rate of reaction for the copper-catalysed coupling reactions to form C–N bonds between aryl hal...
Electron-rich arenes such as anisole, dialkylbenzenes, and aniline and aryl ether derivs. underwent ...
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
DMPAO has been found to be a powerful ligand to enable copper-catalyzed coupling of aryl halides wit...
<i>N</i>-Substituted indoles are synthesized from primary amines through a tandem reaction sequence....
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C–N bon...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
A copper-catalyzed intramolecular amidation of unactivated C(sp(3))-H bonds to construct indoline de...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
The Larsen group specializes in maximizing the potential of simple organic substrates through single...
Indole-carboxylates are N-arylated with 2-bromopyridines using stoichiometric copper(II) oxide/potas...
International audienceA mini-review describes the development of the catalysis by Cu(I) complexes ai...
A versatile protocol for the C–H chalcogenation of indolines and indoles by means of copper catalysi...
The rate of reaction for the copper-catalysed coupling reactions to form C–N bonds between aryl hal...
Electron-rich arenes such as anisole, dialkylbenzenes, and aniline and aryl ether derivs. underwent ...
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
DMPAO has been found to be a powerful ligand to enable copper-catalyzed coupling of aryl halides wit...