A rapid, transition metal-free, high-yielding, tetrabutylammonium bromide-promoted method of N-arylation is reported within. The optimized conditions tolerated a wide range of secondary amines and was equally effective with bromo- and chlorobenzene-including substituted aryl halides. The developed method is found to be effective for N-arylation when compared to earlier methods which involve harsh conditions, transition metals, lack of scalability, and long reaction times. Our method utilizes conventional heating only; it is readily scalable; and the products are facile to purify
Herein, we disclose the first <i>metal-free</i> synthesis of primary aromatic amines from arylboroni...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
A two-step one pot, experimentally simple protocol, based on readily available and inexpensive reage...
A simple and reliable reaction protocol for the clean, fast, and high-yielding synthesis of various ...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
A selective, simple and cost-effective method for the redn. of nitroarenes by Sb metal powder in th...
N-Arylated aliphatic and aromatic amines are important substituents in many biologically active comp...
This thesis details investigations and the optimisation of N-arylation reactions using preciousmetal...
N-Arylated aliphatic and aromatic amines are important substituents in many biologically active comp...
A simple copper salt catalyzed N-arylation reaction with arylboronic acids is reported. In the prese...
A novel and efficient synthesis of N-arylamines by the reaction of activated aryl halides with secon...
A transition-metal-free, regioselective direct aryl–aryl bond-forming process for the synthesis of h...
Since the word “organocatalysis” has been created by MacMillan in 2000, it has growing very fast and...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
Herein, we disclose the first <i>metal-free</i> synthesis of primary aromatic amines from arylboroni...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
A two-step one pot, experimentally simple protocol, based on readily available and inexpensive reage...
A simple and reliable reaction protocol for the clean, fast, and high-yielding synthesis of various ...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
A selective, simple and cost-effective method for the redn. of nitroarenes by Sb metal powder in th...
N-Arylated aliphatic and aromatic amines are important substituents in many biologically active comp...
This thesis details investigations and the optimisation of N-arylation reactions using preciousmetal...
N-Arylated aliphatic and aromatic amines are important substituents in many biologically active comp...
A simple copper salt catalyzed N-arylation reaction with arylboronic acids is reported. In the prese...
A novel and efficient synthesis of N-arylamines by the reaction of activated aryl halides with secon...
A transition-metal-free, regioselective direct aryl–aryl bond-forming process for the synthesis of h...
Since the word “organocatalysis” has been created by MacMillan in 2000, it has growing very fast and...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
Herein, we disclose the first <i>metal-free</i> synthesis of primary aromatic amines from arylboroni...
A copper-catalyzed electrophilic amination of aryl((2-hydroxymethyl)phenyl)dimethylsilanes with Oacy...
A two-step one pot, experimentally simple protocol, based on readily available and inexpensive reage...