4.8 Article

Azidofluoroalkylation of Alkenes with Simple Fluoroalkyl Iodides Enabled by Photoredox Catalysis

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ORGANIC LETTERS
卷 19, 期 18, 页码 4738-4741

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02056

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资金

  1. National Basic Research Program of China (973 Program) [2015CB856600]
  2. National Natural Science Foundation of China [21325206, 21632001]
  3. National Young Top-notch Talent Support Program
  4. Peking University Health Science Center [BMU20160541]

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A mild and efficient protocol for photoredox-catalyzed azidofluoroalkylation of simple alkenes is described with readily available fluoroalkyl iodides. This method allows for a direct and regioselective formation of C-R-F and C-N-3 bonds from the C=C moiety. A variety of fluoroalkyl groups including the CF3 group can be selectively introduced to olefins to afford a series of,beta-fluoroalkylated azides.

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