58995-86-1

Upstream product

• 19591-17-4 o-iodoacetanilide 
• 52670-38-9 2-ethynylaniline 
• 1301267-77-5 N-{2-[(2-aminophenyl)ethynyl]phenyl}acetamide 
• 40754-13-0 2-(1-(2-phenylhydrazineylidene)ethyl)aniline 
• 107127-66-2 2-nitrobenzyl 2-nitrophenyl ketone 
• 32566-01-1 2-(2-aminophenyl)-1H-indole 
• 108-24-7 acetic anhydride 
• 631-57-2 Acetyl cyanide 

Downstream Products

• 159021-62-2 6-methylindolo<1,2-c>quinazoline 
• 4295-28-7 6-methyl-11H-indolo[3,2-c]-quinoline 
• 238398-51-1 2-(2-aminophenyl)-3-nitrosoindole 
• 238398-45-3 2-(2-acetylaminophenyl)-3-nitrosoindole 

Relevant academic research and scientific papers

Synthesis of 2-Arylindoles by Rhodium-Catalyzed/Copper-Mediated Annulative Coupling of N-Aryl-2-aminopyridines and Propargyl Alcohols via Selective C-H/C-C Activation

A versatile rhodium-catalyzed/copper-mediated C-H/C-C activation and cascade annulation reaction was described to form 2-arylindole derivatives. Highly selective C-C bond cleavage of ?-substituted tert-propargyl alcohols occurred, together with pyridine-directed ortho C(sp2)-H bond activation, affording a series of 2-arylindoles with yields up to 90%. Subsequent derivations were smoothly conducted to access polyfunctionalized 2-arylindoles, illustrating the potential applications of this method.

Facile assembly of 11 H -indolo[3,2-c]quinoline by a two-step protocol involving a regioselective 6- endo -cyclization promoted by the hendrickson reagent

An expedient approach was developed to construct the 11H-indolo[3,2-c] quinoline scaffold starting from acyclic alkyne substrates. The five- and six-membered nitrogen-containing rings in the tetracyclic skeleton were elaborated efficiently by gold(III)-ca

Derivatives of the new ring system indolo[1,2-c]benzo[1,2,3]triazine with potent antitumor and antimicrobial activity

Derivatives of the new ring system indolo[1,2-c]benzo[1,2,3]triazine 5 were synthesized by diazotization of substituted 2-(2-aminophenyl)indoles followed by an intramolecular coupling reaction of the diazonium group with the indole nitrogen. To obtain the

2-Phenyl-indole derivatives and process for preparing the same

New stabilizers of polymers and co-polymers of vinyl chloride, the said stabilizers being 2-phenyl-indole derivatives corresponding to the formula: STR1 wherein R represents a phenyl radical, an amino group, optionally substituted by an acetyl or benzoyl