4.8 Article

Merger of C-F and C-N Bond Cleavage in Cross-Electrophile Coupling for the Synthesis of gem-Difluoroalkenes

Journal

ORGANIC LETTERS
Volume 22, Issue 14, Pages 5347-5352

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c01592

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Funding

  1. National Natural Science Foundation of China [21772183]
  2. Fundamental Research Funds for the Central Universities [WK2060190086]
  3. 1000-Youth Talents Plan start-up funding
  4. University of Science and Technology of China

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Herein we successfully applied Katritzky salts as the alkyl electrophile in the reductive allylic defluorinative cross-coupling reaction with alpha-trifluoromethyl alkenes. The merger of C-F and C-N bond cleavage via the synergistic effect of nickel and zinc allows the efficient synthesis of diverse gem-difluor-oalkenes with a good tolerance for various functional groups.

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