Silver(I)-Catalyzed Addition of Phenols to Alkyne Cobalt Cluster Stabilized Carbocations

Carolina Valderas, Luis Casarrubios, Agusti Lledos, Manuel A. Ortuño, María C. de la Torre, Miguel A. Sierra

Research output: Contribution to journalArticleResearchpeer-review

5 Citations (Scopus)

Abstract

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim A smooth catalytic method to use phenols as the nucleophilic partner in the Nicholas reaction has been developed. The method uses either AgIor AuIcatalysts with AgClO4or AgBF4as the most efficient catalysts tested. Neither additional additives nor cocatalysts were required and the formation of the corresponding phenol adducts occurred in excellent yields. The process has the single limitation of the inability of less nucleophilic phenols (4-nitrophenol) to generate the corresponding adducts. Additionally, the reaction is highly diastereoselective. DFT calculations allow a catalytic cycle to be proposed that involves trimetallic intermediates; the rate-determining step of the reaction is hydroxy-group elimination in a cobalt–silver trimetallic intermediate.
Original languageEnglish
Pages (from-to)9015-9023
JournalChemistry - A European Journal
Volume22
Issue number26
DOIs
Publication statusPublished - 1 Jan 2016

Keywords

  • density functional calculations
  • homogeneous catalysis
  • Nicholas reaction
  • reaction mechanisms
  • silver

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