Beilstein Journal of Organic Chemistry (Oct 2013)

Regioselective 1,4-trifluoromethylation of α,β-unsaturated ketones via a S-(trifluoromethyl)diphenylsulfonium salts/copper system

  • Satoshi Okusu,
  • Yutaka Sugita,
  • Etsuko Tokunaga,
  • Norio Shibata

DOI
https://doi.org/10.3762/bjoc.9.257
Journal volume & issue
Vol. 9, no. 1
pp. 2189 – 2193

Abstract

Read online

Regioselective conjugate 1,4-trifluoromethylation of α,β-unsaturated ketones by the use of shelf-stable electrophilic trifluoromethylating reagents, S-(trifluoromethyl)diphenylsulfonium salts and copper under mild conditions is described. A wide range of acyclic aryl–aryl–enones and aryl–alkyl–enones were converted into β-trifluoromethylated ketones in low to moderate yields.

Keywords