4.3 Article

Silver-catalyzed Vinylic C-F Bond Activation: Synthesis of 2-Fluoroindoles from β,β-Difluoro-o-sulfonamidostyrenes

Journal

CHEMISTRY LETTERS
Volume 45, Issue 8, Pages 964-966

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.160427

Keywords

C-F bond activation; Silver catalyst; Fluoroindole

Funding

  1. JSPS KAKENHI Grant [JP16H01002, JP16K20939]
  2. Grants-in-Aid for Scientific Research [16K13943, 16K20939, 16H01002, 16H04105] Funding Source: KAKEN

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An electrophilic 5-endo-trig cyclization of beta,beta-difluoro-o-sulfonamidostyrenes was performed in 1,1,1,3,3,3-hexafluoropropan-2-ol using a Ag(I) catalyst and N,O-bis(trimethylsilyl)acetamide. In this process, vinylic C-F bond activation was achieved via silver-catalyzed beta-fluorine elimination, accompanied by C-N bond formation, which led to the synthesis of 2-fluoroindoles.

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