4.8 Article

Palladium-Catalyzed Carbonylative Sonogashira/Annulation Reaction: Synthesis of Indolo[1,2-b]isoquinolines

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ORGANIC LETTERS
卷 24, 期 5, 页码 1201-1206

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c04350

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资金

  1. NSFC [21801225]
  2. Science Foundation for Young Teachers [2019td02]
  3. High-level Talent Research Start-up Project of Wuyi University [2018TP018]
  4. Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme (2019)
  5. Department of Education of Guangdong Province [2020KCXTD036]

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A palladium-catalyzed carbonylative Sonogashira/annulation reaction has been developed for the synthesis of indolo[1,2-b]isoquinolines, which establishes three C-C bonds and a C-N bond in one step.
A palladium-catalyzed carbonylative Sonogashira/annulation reaction for the synthesis of indolo[1,2-b]isoquinolines has been developed. Tetracyclic 6/5/6/6 indoline skeletons were synthesized in moderate to good yields from easily available 2bromo-N-(2-iodophenyl)benzamides and terminal alkynes. Notably, this efficient methodology established three C-C bonds and a C-N bond through a one-step transformation and provided a new method for the synthesis of indolo[1,2-b]isoquinoline derivatives.

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