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    Metal-mediated rearrangements of 3-alkynyl flavone ethers are reported. The overall process involves 5-endo enyne cyclization to a platinum-containing spiro-oxocarbenium intermediate which may be trapped with methanol to produce spirodihydrofurans or further rearranged to afford either allenyl chromanediones or benzofuranones.

    Citation

    Yuan Xiong, Scott E Schaus, John A Porco. Metal-catalyzed cascade rearrangements of 3-alkynyl flavone ethers. Organic letters. 2013 Apr 19;15(8):1962-5

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    PMID: 23574045

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