1173768-39-2

Upstream product

• 123-75-1 pyrrolidine 
• 4264-35-1 2-acetylindole 
• 1173768-14-3 1-{3-[1-(4-methylphenyl)-3-[3-(trifluoromethyl)phenyl]prop-2-ynyl]-1H-indol-2-yl}ethanone 

Relevant academic research and scientific papers

InCl3-assisted one-pot synthesis of 1-aminocarbazoles

A novel InCl3-mediated one-pot reaction leading to 1-aminocarbazoles is reported. Starting from easily available 2-acetyl-1H-indole, the reaction involves the alkylation of C-3 with a prop-2-yn-1-ol followed by a domino aminobenzannulation reac

Lewis Acid mediated aminobenzannulation reactions of δ-ketoalkynes: Synthesis of 1-aminocarbazoles and 9-aminopyrido[1,2-α]indoles

2-Acyl-N-propargylindoles 1 and 2-acyl-3-propargylindoles 5 undergo aminobenzannulation reactions with pyrrolidine in the presence of an appropriate Lewis acid to give 9-aminopyrido[1,2-α]indoles 6 and 1-aminocarbazoles 7, respectively. The selection of t