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- W2401124471 endingPage "2619" @default.
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- W2401124471 abstract "A convenient and facile palladium-catalyzed reaction of [60]fullerene (C60) with 2-aryl cyclic 1,3-dicarbonyl compounds via the enolate-directed sp2 C–H activation and sp3 C–H functionalization has been exploited to synthesize the novel and rare C60-fused spiroindanes for the first time. This reaction is easy to perform with broad substrate scope and provides diversified products in 20–50% yields. A plausible reaction mechanism involving the palladium-catalyzed enolate-directed C–H activation and subsequent cyclization has been proposed, and the electrochemistry of the C60-fused spiroindanes has also been investigated." @default.
- W2401124471 created "2016-06-24" @default.
- W2401124471 creator A5025336032 @default.
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- W2401124471 date "2016-05-18" @default.
- W2401124471 modified "2023-10-18" @default.
- W2401124471 title "Synthesis of [60]Fullerene-Fused Spiroindanes by Palladium-Catalyzed Oxidative Annulation of [60]Fullerene with 2-Aryl Cyclic 1,3-Dicarbonyl Compounds" @default.
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- W2401124471 doi "https://doi.org/10.1021/acs.orglett.6b01043" @default.
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