4.7 Article

A biosynthetically inspired route to substituted furans using the Appel reaction: total synthesis of the furan fatty acid F5

Journal

CHEMICAL COMMUNICATIONS
Volume 53, Issue 47, Pages 6327-6330

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc03229c

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Funding

  1. Loughborough University

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Appel reaction conditions have been harnessed to affect a mild biosynthetically inspired dehydration of endoperoxides to deliver multi-substituted electron rich furans. Unlike traditional dehydrative procedures, this method is metal and acid free, and can be achieved under redox neutral conditions. It is general for a range of aryl and alkyl substituted endoperoxides, and is functional group tolerant. Furthermore, this procedure has been used to deliver an effective total synthesis of the furan fatty acid (FFA) F-5.

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