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• W2312529338 abstract "An intramolecular approach to generate compounds containing an arylnaphthalene lignan scaffold in high yields is presented. It involves a sequential intramolecular electrophilic attack of carbonyl on arylalkyne followed by benzannulation catalyzed by gold salt. AuCl3 in combination with AgSbF6 works better to effect this transformation. Selected products have been converted into arylnaphthalene lactone natural products such as justicidin E, taiwanin C, and retrojusticidin B." @default.
• W2312529338 created "2016-06-24" @default.
• W2312529338 creator A5011743362 @default.
• W2312529338 creator A5056079142 @default.
• W2312529338 date "2011-11-14" @default.
• W2312529338 modified "2023-10-12" @default.
• W2312529338 title "Synthesis of Arylnaphthalene Lignan Scaffold by Gold-Catalyzed Intramolecular Sequential Electrophilic Addition and Benzannulation" @default.
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• W2312529338 doi "https://doi.org/10.1021/jo201918d" @default.
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