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- W3047478442 endingPage "21202" @default.
- W3047478442 startingPage "21195" @default.
- W3047478442 abstract "Abstract The development of concise, sustainable, and cost‐effective synthesis of aryltetralin lignans, bearing either a fused lactone or cyclic ether, is of significant medicinal importance. Reported is that in the presence of Fukuzumi's acridinium salt under blue LED irradiation, functionalized dicinnamyl ether derivatives are converted into aryltetralin cyclic ether lignans with concurrent generation of three stereocenters in good to high yields with up to 20:1 diastereoselectivity. Oxidation of an alkene to the radical cation is key to the success of this formal Diels–Alder reaction of electronically mismatched diene and dienophile. Applying this methodology, six natural products, aglacin B, aglacin C, sulabiroin A, sulabiroin B, gaultherin C, and isoshonanin, are synthesized in only two to three steps from readily available biomass‐derived monolignols. A revised structure is proposed for gaultherin C." @default.
- W3047478442 created "2020-08-10" @default.
- W3047478442 creator A5046225712 @default.
- W3047478442 creator A5048571267 @default.
- W3047478442 creator A5078512343 @default.
- W3047478442 date "2020-09-11" @default.
- W3047478442 modified "2023-10-18" @default.
- W3047478442 title "Radical‐Cation Cascade to Aryltetralin Cyclic Ether Lignans Under Visible‐Light Photoredox Catalysis" @default.
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