Facile and efficient synthesis of hydrophenanthren-1(2H)-ones and naphtho[2,1-c]furan-3(1H)-ones by a palladium-catalyzed aryne annulation strategy

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Abstract

Novel palladium-catalyzed carboannulation reactions of arynes with functionalized vinyl iodides are reported. By applying allyl-substituted iodocycloenones and iodofuranones, a series of hydrophenanthren-1(2H)-ones and naphtho[2,1-c]furan-3(1H)-ones were efficiently constructed in one pot under mild conditions. © 2010 Wiley-VCH Verlag GmbH &Co. KGaA, Weinheim.

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Huang, X., Sha, F., & Tong, J. (2010). Facile and efficient synthesis of hydrophenanthren-1(2H)-ones and naphtho[2,1-c]furan-3(1H)-ones by a palladium-catalyzed aryne annulation strategy. Advanced Synthesis and Catalysis, 352(2–3), 379–385. https://doi.org/10.1002/adsc.200900703

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