4.7 Article

Copper-Catalyzed Preparation of Benzo[3,4]indolo[1,2-b]isoquinoline-8-ones and Photoluminescence Exploration

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 85, 期 15, 页码 9614-9621

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00936

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资金

  1. Natural Science Foundation of China [21801096, 21772067]
  2. Natural Science Foundation of Zhejiang Province [LQ18B020005, LY19B020004]
  3. University Student Research Innovation Team of Zhejiang Province [2019R417020]
  4. University Student Research Innovation Team of Jiaxing University [CD8517193146]

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A facile synthesis of benzo[3,4]indolo[1,2-b]-isoquinolin-8-ones is described. Under copper catalysis, the reaction proceeds with a high efficiency and a broad reaction scope. A deuteration experiment shows that the KM value is 2.85. From the results on mechanism studies, copper-catalyzed C-H activation, intramolecular cis-addition of alkynes, and reductive elimination are involved. Moreover, this skeleton is indeed a new fluorophore, and its photophysical properties are also investigated.

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