Trapping of Trifluoromethyl Radical with Enolacetate and in situ Generated Enol

Kenji Uneyama, Kunimasa Ueda

Chemistry Letters · 1988 · 18 citations · 3 references

Concepts

Abstract

Abstract Electrochemically generated trifluoromethyl radical can be trapped with enolacetates and enol generated in situ from β-ketoesters and 1,3-diketones, affording trifluoromethylated active methylene compounds.

References

3