145121-13-7

Upstream product

• 91107-10-7 4,6-dimethoxy-2,3-diphenyl-1H-indole 

Downstream Products

• 145121-23-9 7,9-dimethoxy-6,6-dimethyl-1,2-diphenyl-6H-pyrrolo<3,2,1-ij>quinoline 
• 145121-22-8 7,9-dimethoxy-6-methyl-1,2-diphenyl-6H-pyrrolo<3,2,1-ij>quinoline 
• 145121-21-7 7,9-dimethoxy-1,2-diphenyl-4H-pyrrolo<3,2,1-ij>quinoline 
• 145121-19-3 7-bromo-1-(cyclohex-2-en-1-yl)-4,6-dimethoxy-2,3-diphenylindole 
• 146255-93-8 1-benzyl-7-bromo-4,6-dimethoxy-2,3-diphenylindole 
• 145121-18-2 7-bromo-1-(3'-phenylprop-2'-en-1'-yl)-4,6-dimethoxy-2,3-diphenylindole 
• 145121-15-9 7-bromo-1-(2'-methyl-prop-2'-en-1'-yl)-4,6-dimethoxy-2,3-diphenylindole 
• 145121-20-6 7-bromo-4,6-dimethoxy-2,3-diphenyl-1-(prop-2'-yn-1-yl)indole 
• 145121-14-8 7-bromo-4,6-dimethoxy-2,3-diphenyl-1-(prop-2'-en-1'-yl)indole 

Relevant academic research and scientific papers

Palladium-catalysed intramolecular cyclisation of 7-halo-N-allyl-indoles

The N-allyl substituted-7-bromo-indoles (4-9) and the N-propargyl-7-bromo-indole(10) were prepared from the 7-bromo-indole (3). Compounds (4) and (7) undergo palladium-catalysed cyclisation to the pyrroloquinolines (11) and (13). Similar reactions of comp