syn-Fluoro- and -Oxy-trifluoromethylation of Arylacetylenes
journal contributionposted on 18.11.2017 by Song-Lin Zhang, Hai-Xing Wan, Wen-Feng Bie
Any type of content formally published in an academic journal, usually following a peer-review process.
One-step concurrent fluoro-trifluoromethylation across the triple bond of arylacetylenes in a syn mode is enabled by the collaboration of (phen)CuIII(CF3)3 and CsF that produces chemo-, regio-, and stereoselectively (Z)-α-fluoro-β-CF3 styrenes. This method can be extended to achieve syn-oxy-trifluoromethylation and syn-aryl-trifluoromethylation of alkynes using phenoxides, alkoxides, or phenylboronic acid in place of CsF. It opens up new opportunities for preparing various functionalized trifluoromethylated Z-alkenes and demonstrates the potential of Cu(III)–CF3 complexes in organic synthesis.