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A Biosynthetically Inspired Route to Substituted Furans Using the Appel Reaction: Total Synthesis of the Furan Fatty Acid F5

Chemical communications(2017)

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摘要
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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