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Copper-Catalyzed Directed Hydroindolation/Annulation Sequence of Alkynes with Indoles via Copper Carbenes.

Guang MaQiu-Yue CuiKua-Fei WeiXiao-Lei JiangDong-Can LvXiaoping XueXiu-Hong ZhuGuang-Xin RuXinfeng XieWen-Bo Shen
Published in: Organic letters (2024)
Described herein is an efficient copper-catalyzed tandem alkyne indolylcupration-initiated 1,2-indole migration/6π-electrocyclic reaction of allene-ynamides with indoles by the in situ-generated metal carbenes. This method allows the efficient synthesis of valuable indole-fused spirobenzo[ f ]indole-cyclohexanes with high regio- and stereoselectivity. In addition, this reaction affords rapid access to the functionalized spirobenzo[ f ]indole-cyclohexanes in the absence of indoles by a presumable 5-exo-dig cyclization/Friedel-Crafts alkylation via copper-containing all-carbon 1,4-dipoles.
Keyphrases
  • oxide nanoparticles
  • mass spectrometry