4.6 Article

Gold-Catalyzed Addition of β-Ketoesters to Alkenes: Influence of Electronic and Steric Effects in the Reaction Outcome

Journal

MOLECULES
Volume 23, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/molecules23030629

Keywords

gold catalysis; hydroalkylation; beta-ketoesters; olefins

Funding

  1. CONICET
  2. ANPCyT
  3. Universidad Nacional de Rosario from Argentina (UNR)

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The gold-catalyzed intermolecular hydroalkylation of olefins with beta-ketoesters represents a conceptually attractive and useful synthetic tool; however, it has been scarcely applied, remaining a challenge for chemists. The aim of the current study was to investigate the addition of these 1,3-diketo-compounds to alkenes under gold catalysis conditions, in order to establish the electronic and steric effects of the alkenyl substrates in the reaction outcome. The screening of different catalyst systems and diverse olefins enabled defining the alkenyl requirements and the best reaction conditions to efficiently achieve the coupled products.

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