4.7 Article

Synthesis of Perfluorinated Isoquinolinediones through Visible-Light-Induced Cyclization of Alkenes

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 80, 期 24, 页码 12599-12605

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b01803

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资金

  1. National Natural Science Foundation of China [21462017]
  2. China Postdoctoral Science Foundation [2014M560649]
  3. Hunan Provincial Natural Science Foundation of China [2015112113]
  4. program (Environment and Energy Materials and deep processing of mineral resources in Wuling Mountain) for Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province

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A novel visible-light-induced carboperfluoroalkylation of alkenes using perfluoroalkyl iodides and bromides as R-f sources, leading to isoquinoline-1,3-diones, was developed. This method offers rapid entry to perfluorinated isoquinoline-1,3(2H,4H)-diones from N-alkyl-N-methacryloyl benzamides under mild reaction conditions, allowing for the incorporation of a wide variety of perfluorinated groups such as CF3, C3F7, C4F9, C6F13, C8F17, C10F21, and CF2CO2Et.

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