International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleophilic aromatic substitution of the corresponding aryl halides. The halogen atom is usually relatively inert to amination reaction unless it is activated by the presence of electron withdrawing groups. Consequently, there has been particular emphasis over the past decade on the synthesis of metal complexes that are active catalysts for the preparation of aromatic amines. This tutorial review focuses on the use of metal-based complexes for the direct amination of aryl halides with ammonia
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A highly effective solvent-free protocol for the Buchwald-Hartwig amination of unactivated aryl chlo...
We report the palladium-catalyzed coupling of aryl halides with ammonia and gaseous amines as their ...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
A base-promoted amination of aromatic halides has been developed using a limited amount of dimethylf...
The present report exemplifies two novel aromatic ring amination reactions via metal mediation. A ra...
The present report exemplifies two novel aromatic ring amination reactions via metal mediation. A ra...
A Rh(III)-catalyzed direct aromatic C-H amination is achieved using N-chloroamines as a reagent. Fur...
Highlights• Copper-catalyzed arylation of aqueous ammonia from aromatic halides.• Synthesis of...
A Rh(III)-catalyzed direct aromatic C–H amination is achieved using <i>N</i>-chloroamines as a reage...
Ambidentate ligand pyridyldiketones were used in combination with copper to catalyze amination of ar...
An environmentally friendly and economically favorable approach to the formation of C-N bonds is pre...
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A highly effective solvent-free protocol for the Buchwald-Hartwig amination of unactivated aryl chlo...
We report the palladium-catalyzed coupling of aryl halides with ammonia and gaseous amines as their ...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
International audienceThe traditional homogeneous access to aromatic amine derivatives is a nucleoph...
A base-promoted amination of aromatic halides has been developed using a limited amount of dimethylf...
The present report exemplifies two novel aromatic ring amination reactions via metal mediation. A ra...
The present report exemplifies two novel aromatic ring amination reactions via metal mediation. A ra...
A Rh(III)-catalyzed direct aromatic C-H amination is achieved using N-chloroamines as a reagent. Fur...
Highlights• Copper-catalyzed arylation of aqueous ammonia from aromatic halides.• Synthesis of...
A Rh(III)-catalyzed direct aromatic C–H amination is achieved using <i>N</i>-chloroamines as a reage...
Ambidentate ligand pyridyldiketones were used in combination with copper to catalyze amination of ar...
An environmentally friendly and economically favorable approach to the formation of C-N bonds is pre...
The direct amination of C-H bonds with ammonia is a challenge in synthetic chemistry. Herein, we pre...
A highly effective solvent-free protocol for the Buchwald-Hartwig amination of unactivated aryl chlo...
We report the palladium-catalyzed coupling of aryl halides with ammonia and gaseous amines as their ...