4.7 Article

Photoredox-Catalyzed Deoxygenative Intramolecular Acylation of Biarylcarboxylic Acids: Access to Fluorenones

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 82, Issue 23, Pages 12834-12839

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.7b02197

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Funding

  1. National Natural Science Foundation of China [21474048, 21372114, 21672099, 21462041]

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An efficient deoxygenative radical cyclization reaction has been reported for the synthesis of fluorenones by employing various biarylcarboxylic acids via photoredox catalysis. Attractive features of this process include generation of acyl radical, which quickly underdone intramolecular radical cyclization. This method marks the first photo catalytic intramolecular acyl radical coupling for constructing carbon-carbon bond, which further synthesizes the valuable fluorenone products with mild conditions, good yields, and good functional-group compatibility.

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