Polychloromethylative cyclization of -alkenyl indoles was developed under metal-free conditions to afford tricyclic pyridoindolones and pyrroloindolones in moderate to good yields. In the reaction, commercially available CHCl and CHCl were employed as tri- and dichloromethyl radical sources. Moreover, tri- and dichloromethylated polycyclic benzoimidazoles can also be obtained under standard conditions.
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http://dx.doi.org/10.1039/d3ob01191g | DOI Listing |
Org Biomol Chem
September 2023
School of Petrochemical Engineering, Changzhou University, Changzhou 213164, P. R. China.
Polychloromethylative cyclization of -alkenyl indoles was developed under metal-free conditions to afford tricyclic pyridoindolones and pyrroloindolones in moderate to good yields. In the reaction, commercially available CHCl and CHCl were employed as tri- and dichloromethyl radical sources. Moreover, tri- and dichloromethylated polycyclic benzoimidazoles can also be obtained under standard conditions.
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