<div><p></p><p>We report here a simple, efficient, and environmentally friendly methodology for electrophilic aryl-iodination of electron-rich arenes using I<sub>2</sub>-oxone under ball milling. The reactions work efficiently under solvent-free conditions at room temperature. We have also shown that iodine could be used as catalyst for metal-free biaryl coupling of a few electron-rich substrates. In addition, one-pot multistep synthesis has been demonstrated for one substrate.</p> </div
A halogen bond-assisted electron-catalyzed iodination of heteroarenes has been developed for the fir...
A metal-free and efficient approach to N-arylpyrrolidines from arylamines and cyclic ethers catalyze...
The front cover picture, provided by Burkhard Konig et al., illustrates how iodine solutions block m...
Iodoarenes are important precursors for fine chemicals and pharmaceuticals. The direct iodination of...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Six easy laboratory procedures are presented for the oxidative iodination ofvarious aromatics, mostl...
A fast and site-selective biaryl synthesis via dehydrogenative C–H/C–H arylation in a ball mill was ...
The direct functionalization of C-H bonds has drawn the attention of chemists for almost a century. ...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
A novel, mild, and practical method of amination of simple nonfunctionalized arenes under metal free...
A facile synthesis of diaryliodonium salts utilizing Oxone as versatile and cheap oxidant has been d...
Recognizing the need for efficient routes to biaryl compounds, chemists have developed an arsenal of...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
A halogen bond-assisted electron-catalyzed iodination of heteroarenes has been developed for the fir...
A metal-free and efficient approach to N-arylpyrrolidines from arylamines and cyclic ethers catalyze...
The front cover picture, provided by Burkhard Konig et al., illustrates how iodine solutions block m...
Iodoarenes are important precursors for fine chemicals and pharmaceuticals. The direct iodination of...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Six easy laboratory procedures are presented for the oxidative iodination ofvarious aromatics, mostl...
A fast and site-selective biaryl synthesis via dehydrogenative C–H/C–H arylation in a ball mill was ...
The direct functionalization of C-H bonds has drawn the attention of chemists for almost a century. ...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
A novel, mild, and practical method of amination of simple nonfunctionalized arenes under metal free...
A facile synthesis of diaryliodonium salts utilizing Oxone as versatile and cheap oxidant has been d...
Recognizing the need for efficient routes to biaryl compounds, chemists have developed an arsenal of...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
A halogen bond-assisted electron-catalyzed iodination of heteroarenes has been developed for the fir...
A metal-free and efficient approach to N-arylpyrrolidines from arylamines and cyclic ethers catalyze...
The front cover picture, provided by Burkhard Konig et al., illustrates how iodine solutions block m...