Trapping of Trifluoromethyl Radical with Enolacetate and in situ Generated Enol
- 5 May 1988
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 17 (5) , 853-854
- https://doi.org/10.1246/cl.1988.853
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.This publication has 5 references indexed in Scilit:
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