97227-64-0

Upstream product

• 54655-08-2 N,N-dimethyl-2-(2-phenylethynyl)aniline 
• 171364-80-0 methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 
• 536-74-3 phenylacetylene 
• 93503-51-6 methyl 4-(2-phenyl-1H-indol-3-yl)-3-cyclohexene-1-carboxylate 
• 93503-50-5 4-(2-phenyl-1H-indol-3-yl)-3-cyclohexene-1-carboxylic acid 
• 874-61-3 4-oxocyclohexanecarboxylic acid 
• 948-65-2 2-phenyl-indole 
• 93503-57-2 methyl 4-(1-methyl-2-phenyl-1H-indol-3-yl)-3-cyclohexene-1-carboxylate 

Downstream Products

• 93503-75-4 4-(1-methyl-2-phenyl-1H-indol-3-yl)-benzoic acid 

Relevant academic research and scientific papers

Palladium-Catalyzed Synthesis of 2,3-Diaryl- N-methylindoles from ortho-Alkynylanilines and Aryl Pinacol Boronic Esters

A palladium-catalyzed synthesis of 2,3-diaryl-N-methylindoles from o-alkynylanilines and aryl pinacol boronic esters was developed. The system possesses high functional group tolerance and a broad substrate scope with a variety of aryl pinacol boronic est

Syntheses and complement inhibitory activities of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids

The syntheses of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids are described. These compounds express potent in vitro inhibition of the human classical complement pathway, and qualitative SAR have been determined. Several of the in vitro active