4.7 Article

Catalytic One-Step Deoxytrifluoromethylation of Alcohols

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 84, Issue 4, Pages 2061-2071

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.8b03072

Keywords

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Funding

  1. Herman Frasch Foundation for Chemical Research [701-HF12]
  2. National Science Foundation [CHF-1455163]
  3. NIGMS Training Grant on Dynamic Aspects of Chemical Biology [T32 GM08545]
  4. NIH [S10OD016360, S10RR024664]
  5. NSF [9977422, 0320648]
  6. NIH Center Grant [P20GM103418]

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A new bench-stable trifluoromethylation reagent, phenyl bromodifluoroacetate, converts readily available alcohols to trifluoromethanes in a Cu-catalyzed deoxytrifluoromethylation reaction. This reaction streamlines access to target biologically active molecules, and should be useful for a variety of medicinal, agricultural, and materials chemists.

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