Direct arylation of unactivated arenes or heteroarenes with aryl halides could be carried out in the presence of potassium <i>tert</i>-butoxide and dimethyl sulfoxide under visible-light irradiation. Ir(ppy)<sub>3</sub> was found to be an effective photoredox catalyst for this reaction. The reactions of aryl iodides occurred at room temperature. Elevated temperature was required for aryl bromides. Homolytic aromatic substitution was proposed to be the operative reaction pathway
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and f...
Visible light along with 1 mol % eosin Y catalyzes the direct C-H bond arylation of heteroarenes wit...
We developed a simple and convenient method to assemble biaryls exploiting a photoredox catalyst and...
This chapter provides an overview over the recent developments and the early examples of functionali...
Introducing aryl- and heteroaryl moieties into molecular scaffolds are often key steps in the synthe...
A reaction of aromatic halides bearing electron-withdrawing groups with tertiary amines in the prese...
Herein is a pertinent review of recent photochemical homolytic aromatic substitution (HAS) literatur...
From PubMed via Jisc Publications RouterPublication status: epublishA ruthenium-catalyzed C-H aryl...
Conceptually different approach toward biaryl syntheses by photoinduced direct CH arylation of benze...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Visible light and eosin Y catalyze the direct arylation of simple arenes with fluorinated aryl bromi...
The use of a dual palladium/organic photoredox catalytic system enables the directed arylation of ar...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and f...
Visible light along with 1 mol % eosin Y catalyzes the direct C-H bond arylation of heteroarenes wit...
We developed a simple and convenient method to assemble biaryls exploiting a photoredox catalyst and...
This chapter provides an overview over the recent developments and the early examples of functionali...
Introducing aryl- and heteroaryl moieties into molecular scaffolds are often key steps in the synthe...
A reaction of aromatic halides bearing electron-withdrawing groups with tertiary amines in the prese...
Herein is a pertinent review of recent photochemical homolytic aromatic substitution (HAS) literatur...
From PubMed via Jisc Publications RouterPublication status: epublishA ruthenium-catalyzed C-H aryl...
Conceptually different approach toward biaryl syntheses by photoinduced direct CH arylation of benze...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Visible light and eosin Y catalyze the direct arylation of simple arenes with fluorinated aryl bromi...
The use of a dual palladium/organic photoredox catalytic system enables the directed arylation of ar...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
The facile iodination of aromatic compounds under mild conditions is a great challenge for both orga...
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and f...
Visible light along with 1 mol % eosin Y catalyzes the direct C-H bond arylation of heteroarenes wit...