Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C–N bond formation/intramolecular cross-dehydrogenative coupling process at 130 °C in DMSO. The methodology allows practical and modular assembly of indoles in good to excellent yields from readily available aryl iodides and enamines
A new strategy for direct and highly efficient synthesis of 2,3′-bisindolin-3-ones has been develope...
The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcone...
A versatile protocol for the C–H chalcogenation of indolines and indoles by means of copper catalysi...
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
<i>N</i>-Substituted indoles are synthesized from primary amines through a tandem reaction sequence....
A Cu-diamine complex effectively catalyses tandem C-N bond formation on 2-(2-haloalkenyl)-aryl halid...
A sequential Rh<sub>2</sub>(OAc)<sub>4</sub>-catalyzed multicomponent reaction and CuCl<sub>2</sub>-...
Symmetrical 3,3-diaryl-2-iminoindoles were prepared from 3-diazoindolin-2-imines and indoles via a c...
CuCl2-mediated intramolecular C-H/C-H cross-dehydrogenative coupling (CDC) of thioalkyl-substituted ...
Herein, we developed a copper-catalyzed O-vinylation of arylhydroxylamine using vinyliodonium salts ...
An efficient and convenient synthesis of a variety of decorated indoles using a three-component tand...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
An efficient one-pot cascade to indoles and related fused heterocycles has been demonstrated in rene...
An efficient and economical synthetic approach toward 3-cyano-1<i>H</i>-indoles through the reaction...
A monoalkoxy phenyl group as a dummy ligand on indolyl(aryl)iodonium imides, which is related to t...
A new strategy for direct and highly efficient synthesis of 2,3′-bisindolin-3-ones has been develope...
The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcone...
A versatile protocol for the C–H chalcogenation of indolines and indoles by means of copper catalysi...
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
<i>N</i>-Substituted indoles are synthesized from primary amines through a tandem reaction sequence....
A Cu-diamine complex effectively catalyses tandem C-N bond formation on 2-(2-haloalkenyl)-aryl halid...
A sequential Rh<sub>2</sub>(OAc)<sub>4</sub>-catalyzed multicomponent reaction and CuCl<sub>2</sub>-...
Symmetrical 3,3-diaryl-2-iminoindoles were prepared from 3-diazoindolin-2-imines and indoles via a c...
CuCl2-mediated intramolecular C-H/C-H cross-dehydrogenative coupling (CDC) of thioalkyl-substituted ...
Herein, we developed a copper-catalyzed O-vinylation of arylhydroxylamine using vinyliodonium salts ...
An efficient and convenient synthesis of a variety of decorated indoles using a three-component tand...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
An efficient one-pot cascade to indoles and related fused heterocycles has been demonstrated in rene...
An efficient and economical synthetic approach toward 3-cyano-1<i>H</i>-indoles through the reaction...
A monoalkoxy phenyl group as a dummy ligand on indolyl(aryl)iodonium imides, which is related to t...
A new strategy for direct and highly efficient synthesis of 2,3′-bisindolin-3-ones has been develope...
The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcone...
A versatile protocol for the C–H chalcogenation of indolines and indoles by means of copper catalysi...