1262302-60-2

Upstream product

• 1173153-20-2 2-((4-fluorophenyl)ethynyl)benzeneamine 
• 615-43-0 2-iodophenylamine 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 948-65-2 2-phenyl-indole 
• 782-17-2 2-(4-fluorophenyl)indole 
• 55577-25-8 2-(4-methylphenyl)-1H-indole 
• 131298-21-0 2-[(2-aminophenyl)ethynyl]phenylamine 
• 459-57-4 4-fluorobenzaldehyde 

Relevant academic research and scientific papers

Carbocatalysed Oxidative C sp 2 -C sp 2 Homocouplings of Benzo-Fused Heterocycles

Appropriate and fine-tuned treatments of amorphous carbon (AC) involving aqua regia or concentrated HNO3 lead to oxidised carbon materials (oAC) which are able to catalyse 2,2′- and 3,3′-homocouplings of various functionalised indoles with outs

Bronsted acid catalyzed cascade reactions of 2-[(2-Aminophenyl) ethynyl]phenylamine derivatives with aldehydes: A new approach to the synthesis of 2,2′-disubstituted 1 H,1′ H -3,3′-biindoles

An unusual Bronsted acid catalyzed cascade reaction of 2-[(2-aminophenyl)ethynyl]phenylamine derivatives with aryl(heteroaryl)aldehydes to afford an efficient alternative entry into 2,2′-disubstituted-1H, 1′H-3,3′-biindoles under metal-free conditions is reported.

Cycloisomerization of 2-alkynylanilines to indoles catalyzed by carbon-supported gold nanoparticles and subsequent homocoupling to 3,3′-biindoles

Elevated by the support: 2-Alkynyl aniline cycloisomerization to indole is catalyzed by cationic Au NPs on a carbon support. Electroneutral and rich 2-aryl indoles are further converted into 3,3′-biindoles by oxidative homocoupling that is readily catalyzed by the Au NPs on carbon, and exclusively but also somewhat sluggishly by the carbon support. Copyright

Iron-catalyzed oxidative homo-coupling of indoles via C-H cleavage

A new method for the homo-coupling of indoles has been developed by the use of FeCl3 as catalyst and molecular oxygen as the only oxidant. The protocol provides a practical and straightforward approach toward 3, 3'-biindolyls.