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• W2320726429 endingPage "2120" @default.
• W2320726429 startingPage "2116" @default.
• W2320726429 abstract "An efficient one-pot synthesis of functionalized chromones from ketone derivatives and o-haloaroyl chlorides was achieved using a combination of two bases under transition-metal-free conditions. This formal [3+3] cycloaddition consists of a sequential C-acylation and O-arylation, which is amenable to a broad range of substrates leading to diversely functionalized chromones in moderate to high yields. Notably, the utility of this methodology was demonstrated by a two-step concise synthesis of frutinone A." @default.
• W2320726429 created "2016-06-24" @default.
• W2320726429 creator A5066546362 @default.
• W2320726429 creator A5082986499 @default.
• W2320726429 creator A5090224970 @default.
• W2320726429 date "2016-05-01" @default.
• W2320726429 modified "2023-09-25" @default.
• W2320726429 title "Efficient synthesis of functionalized chromones via a two-base mediated formal [3+3] cycloaddition" @default.
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• W2320726429 doi "https://doi.org/10.1016/j.tetlet.2016.04.010" @default.
• W2320726429 hasPublicationYear "2016" @default.
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