4.8 Article

Synthesis of Benzofuran Derivates via a Gold-Catalyzed Claisen Rearrangement Cascade

Journal

ORGANIC LETTERS
Volume 24, Issue 31, Pages 5829-5834

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c02388

Keywords

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Funding

  1. Natural Science Foundation of China and Shandong Province [21971149, 92156007, ZR2019ZD45, ZR2020KB005]
  2. Fundamental Research Funds of Shandong University

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A novel method for synthesizing diverse benzofuran derivatives from easily obtained quinols and alkynyl esters has been reported. The method involves a gold-catalyzed intermolecular alkoxylation/Claisen rearrangement/condensation cascade. The introduction of difluorodiphenylsilane as a water-trapping reagent in the reaction leads to higher yield.
A novel method toward a facile synthesis of diverse benzofuran derivates from easily obtained quinols and alkynyl esters has been reported. A gold-catalyzed intermolecular alkoxylation/Claisen rearrangement/condensation cascade was involved. The introduction of difluorodiphenylsilane as a water-trapping reagent in the reaction leads to a higher yield.

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