Electrochemical bromocyclization enables 3,5-diversification of heterocyclic indolines
Hai Ren,
Rui-An Wang,
Jun Shi
et al.
Abstract:We report a protonic-acid-promoted electrosynthetic strategy for the dearomative dibromocyclization of tryptamine/tryptophol derivatives for the convenient late-stage 3,5-diversification of heterocyclic indolines.
A novel TEA-mediated cascade arylation/cyclization reaction between indole acetamides and 3-substituted indoles for the synthesis of various indolyl pyrroloindolines has been developed.
A novel TEA-mediated cascade arylation/cyclization reaction between indole acetamides and 3-substituted indoles for the synthesis of various indolyl pyrroloindolines has been developed.
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