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- W2005359171 abstract "A new oxygen-centered radical cyclization onto silyl enol ethers has been developed and utilized for the synthesis of versatile siloxy-substituted tetrahydrofurans. The reactions display excellent chemoselectivity for cyclization onto the electron-rich silyl enol ether when competing terminal alkene cyclization, 1,5-hydrogen abstraction, and beta-fragmentation pathways are present. The increased chemoselectivity also allows for the synthesis of tetrahydropyrans, a challenging substrate class to access using oxygen-centered radical alkene cyclizations due to competing 1,5-hydrogen abstractions." @default.
- W2005359171 created "2016-06-24" @default.
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- W2005359171 date "2009-03-31" @default.
- W2005359171 modified "2023-09-26" @default.
- W2005359171 title "ChemInform Abstract: Chemoselective Oxygen-Centered Radical Cyclizations onto Silyl Enol Ethers." @default.
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- W2005359171 doi "https://doi.org/10.1002/chin.200913097" @default.
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