Gold-catalyzed cycloisomerization of (2-Alkynyl-1-cycloalkenyl)methanols to highly substituted furans

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Abstract

A new and efficient Au-catalyzed alkoxycyclization of conjugated enynols offers a general entry to a wide range of highly substituted furans in good to excellent yields. These furans were subjected to diethyl acetylenedicarcoxylate to afford the interesting cycloadducts in good to excellent yields.

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Oh, C. H., Yi, H. J., & Lee, K. H. (2010). Gold-catalyzed cycloisomerization of (2-Alkynyl-1-cycloalkenyl)methanols to highly substituted furans. Bulletin of the Korean Chemical Society, 31(3), 683–688. https://doi.org/10.5012/bkcs.2010.31.03.683

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