Abstract:The iodine-promoted cyclization of various N-(2-CF3-2-NHTs)ethylbenzimidazoles and N-(2-CF3-2-NHTs)ethylindoles proceeded smoothly and efficiently under mild basic conditions.
“…13 Therefore, the synthesis of 2-trifluoromethylindolines and 2-trifluoromethylindoles has recently attracted much attention, and various approaches have been reported. 14…”
A SmI2-mediated reductive cyclisation using trifluoroacetamide groups as radical precursors and alkynes as radical acceptors, which is the first example of using an acyclic amide group in a reductive cyclisation, afforded 2-trifluoromethylindolines.
“…13 Therefore, the synthesis of 2-trifluoromethylindolines and 2-trifluoromethylindoles has recently attracted much attention, and various approaches have been reported. 14…”
A SmI2-mediated reductive cyclisation using trifluoroacetamide groups as radical precursors and alkynes as radical acceptors, which is the first example of using an acyclic amide group in a reductive cyclisation, afforded 2-trifluoromethylindolines.
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