Transition-metal-catalyzed amination of aryl halides is one of the most employed methods
for constructing N-arylation adducts. However, the broad success of these reactions largely …

We report a mild method for the copper-catalyzed amination of aryl chlorides. Key to the
success of the method was the use of highly sterically encumbered N 1, N 2-diaryl diamine …

Transition metal catalysis is crucial for the synthesis of complex molecules, with ligands and
bases playing a pivotal role in optimizing cross-coupling reactions. Despite advancements …

Transition metal-catalyzed cross-coupling reactions are essential in modern organic
synthesis, facilitating the rapid creation of complex molecular structures. Traditionally, these …

The synthesis of (iso) quinoline-indole hybrids by reacting (iso) quinoline N-oxides with o-
alkynylanilines in the presence of a combination of copper (II) catalyst and a bidentate 2, 2 …

CuI/6-hydroxy picolinohydrazide-catalyzed coupling of (hetero) aryl chlorides with anilines
proceeded well at 100° C to afford biaryl amines in a diverse manner, which represents the …

Poly (arylene ether) s (PAEs) are a versatile class of thermoplastic materials with
commercial importance. Currently their synthesis relies predominantly on either nucleophilic …

Herein, an approach for synthesizing 2-amino-3-substituted quinoline-4 (3 H)-ones and N-
phenylbenzamide derivatives was developed. A series of quinoline-4 (3 H)-ones were …

The aryloxyamine motif is a prominent pharmacophore in drug design and development.
While these biologically relevant structures could in principle be sustainably assembled from …

Nickel-catalyzed cross-couplings of alcohols/amines with aryl halides enable the
challenging chemoselective O-or N-arylation of complex substrates concurrently containing …