The reaction of electron-rich arenes with alkali metal bromides such as sodium and potassium bromides in the presence of cone. H2SO 4 to give p-bromoarenes is reported. The reaction is possible in the absence of any specialised oxidising agents and the yields are high
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium te...
The reaction of electron-rich arenes with alkali metal bromides such as sodium and potassium bromid...
Arenes undergo electrophilic substitution reaction when treated with tetraalkylammonium halides (bro...
357-360Arenes undergo electrophilic substitution reaction when treated with tetraalkylammonium hal...
Brominated arenes are versatile intermediates in the synthesis of a wide variety of biologically act...
The estimated excited oxidation potential of sodium anthraquinone-2-sulfonate (SAS) increases from 1...
A mild, metal-free bromination method of arenes has been developed using the combination of bis(trif...
An efficient and practical system for inexpensive bromination and iodination of arenes as well as he...
An efficient and practical system for inexpensive bromination and iodination of arenes as well as he...
Transition metal-free couplings of haloarenes with arenes, triggered by the use of alkali metal alko...
An efficient, simple and regioselective monobromination of least reactive acyclic and cyclic alkanes...
Abstract- A facile, efficient, simple, environmentally safe, regioselective, controllable and econom...
Highly deactivated aromatic compounds were smoothly monobrominated by treatment with N-bromosuccinim...
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium te...
The reaction of electron-rich arenes with alkali metal bromides such as sodium and potassium bromid...
Arenes undergo electrophilic substitution reaction when treated with tetraalkylammonium halides (bro...
357-360Arenes undergo electrophilic substitution reaction when treated with tetraalkylammonium hal...
Brominated arenes are versatile intermediates in the synthesis of a wide variety of biologically act...
The estimated excited oxidation potential of sodium anthraquinone-2-sulfonate (SAS) increases from 1...
A mild, metal-free bromination method of arenes has been developed using the combination of bis(trif...
An efficient and practical system for inexpensive bromination and iodination of arenes as well as he...
An efficient and practical system for inexpensive bromination and iodination of arenes as well as he...
Transition metal-free couplings of haloarenes with arenes, triggered by the use of alkali metal alko...
An efficient, simple and regioselective monobromination of least reactive acyclic and cyclic alkanes...
Abstract- A facile, efficient, simple, environmentally safe, regioselective, controllable and econom...
Highly deactivated aromatic compounds were smoothly monobrominated by treatment with N-bromosuccinim...
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromid...
Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium te...
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