4.0 Article

Highly Substituted Lactone/Ester-Containing Furan Library by the Palladium-Catalyzed Carbonylation of Hydroxyl-Substituted 3-lodofurans

Journal

ACS COMBINATORIAL SCIENCE
Volume 13, Issue 3, Pages 272-279

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/co100088q

Keywords

iodocyclization; nucleophile; carboalkoxylation; cyclocarbonylation; furan

Funding

  1. National Institute of General Medical Sciences [GM070620, GM079593]
  2. National Institutes of Health Kansas University Chemical Methodologies and Library Development Center of Excellence [GM069663]

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Highly substituted lactone- and ester-containing furans have been prepared by the efficient palladium-catalyzed intramolecular cyclocarbonylation or intermolecular carboalkoxylation, respectively, of hydroxyl-containing 3-iodofurans, readily prepared by the iodocyclization of 2(1-alkynyl)-2-alken-1-ones in the presence of various diols.

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