Nickel-catalysed electroreductive coupling of α-halogenoesters with aryl or vinyl halides
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 1,p. 48-49
- https://doi.org/10.1039/c39900000048
Abstract
β, γ-Unsaturated esters are obtained in moderate to good yields by a one-step electrochemical procedure from α-chloroesters and aryl or vinyl halides; a sacrificial aluminium anode, dimethylformamide as solvent, and a catalytic amount of nickel bromide-2,2′-bipyridine complex are used.Keywords
This publication has 6 references indexed in Scilit:
- Synthèse électrochimique d'esters arylacétique et arylpropionique via des complexes du nickelJournal of Organometallic Chemistry, 1988
- A New Convenient Synthesis of α-Arylpropionic Acid Esters and α-ArylpropionitrilesSynthetic Communications, 1986
- Electrosynthesis of carboxylic acids from organic halides and carbon dioxideTetrahedron Letters, 1985
- Nickel-catalyzed synthesis of arylacetic esters from arylzinc chlorides and ethyl bromoacetateOrganometallics, 1983
- Catalysis of the arylation of the reformatsky reagent by palladium or nickel complexes. Synthesis of aryl acid estersJournal of Organometallic Chemistry, 1979
- A nickel catalyst for the arylation and vinylation of lithium ester enolatesJournal of the American Chemical Society, 1977