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• W2108588321 abstract "The preparation of annulated furan systems as key synthetic intermediates through the application of a two-step annulation involving an electrochemical ring closure between a furan and a silyl enol ether has been studied. The reaction was shown to be quite general for the formation of six-membered rings in good yields and was tolerant of a variety of different functional groups. The ring closure was highly stereoselective, leading to the formation of cis-fused systems. Cyclic voltammetry and probe molecules were used to gain mechanistic insight into the reaction. These studies suggested that the key ring closure involved an initial oxidation of the silyl enol ether to a radical cation followed by a furan-terminated cyclization." @default.
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• W2108588321 date "2004-04-28" @default.
• W2108588321 modified "2023-10-08" @default.
• W2108588321 title "Electrooxidative Coupling of Furans and Silyl Enol Ethers: Application to the Synthesis of Annulated Furans" @default.
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• W2108588321 doi "https://doi.org/10.1021/jo049889i" @default.
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