The facile iodination of aromatic compounds under mild conditions is a great challenge for both organic and medicinal chemistry. Particularly, the synthesis of functionalized aryl iodides by light has long been considered impossible due to their photo-lability, which actually makes aryl iodides popular starting materials in many photo-substitution reactions. Herein, a photo-induced halogen exchange in aryl or vinyl halides has been discovered for the first time. A broad scope of aryl iodides can be prepared in high yields at room temperature under exceptionally mild conditions without any metal or photo-redox catalysts. The presence of a catalytic amount of elemental iodine could promote the reaction significantly
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
A metal-free photoredox C–H alkylation of heteroaromatics from readily available carboxylic acids us...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
The central theme of this thesis is the development of new metal-catalyst-free reactions promoted by...
Direct arylation of unactivated arenes or heteroarenes with aryl halides could be carried out in the...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
A protocol for photoinduced cross-coupling of aryl iodides having polar π-functional groups or elong...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
The quantum yields of I*(2P1/2) production from iodobenzene and pentafluoroiodobenzene at five diffe...
A metal- and base-free method is developed for the synthesis of aryl iodides from arylhydrazine hydr...
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and f...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
Aryl and alkenyl iodides are important intermediates for value-added targets in organic synthesis an...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
A metal-free photoredox C–H alkylation of heteroaromatics from readily available carboxylic acids us...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
The central theme of this thesis is the development of new metal-catalyst-free reactions promoted by...
Direct arylation of unactivated arenes or heteroarenes with aryl halides could be carried out in the...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
A protocol for photoinduced cross-coupling of aryl iodides having polar π-functional groups or elong...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
A visible-light-mediated atom transfer radical cyclization of unactivated alkyl iodides is described...
The quantum yields of I*(2P1/2) production from iodobenzene and pentafluoroiodobenzene at five diffe...
A metal- and base-free method is developed for the synthesis of aryl iodides from arylhydrazine hydr...
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and f...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
Aryl and alkenyl iodides are important intermediates for value-added targets in organic synthesis an...
The work being presented in this paper demonstrates the simple and efficient “transition-metal-free”...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
A metal-free photoredox C–H alkylation of heteroaromatics from readily available carboxylic acids us...