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Palladium-Catalyzed α-Arylation of Zinc Enolates of Esters: Reaction Conditions and Substrate Scope

[Image: see text] The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc enolates of esters is reported. Reactions of three different types of zinc enolates have been developed. α-Arylation of esters occurs in high yields with isolated Reformatsky reagent...

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Bibliografische gegevens
Hoofdauteurs: Hama, Takuo, Ge, Shaozhong, Hartwig, John F.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2013
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3800138/
https://ncbi.nlm.nih.gov/pubmed/23931445
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo401476f
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