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• W2418106836 abstract "With the promotion of Lewis acid BF(3)•OEt(2), various N-(hex-5-enyl)-2-iodoalkanamides underwent efficient and regioselective 9-endo iodine-atom-transfer radical cyclization reactions at room temperature. The cyclized products were readily converted to the corresponding azonan-2-ones by reduction with Bu(3)SnH or to hexahydroindolizin-3(5H)-ones by treatment with aqueous Na(2)CO(3) in a one-pot, two-stage manner." @default.
• W2418106836 created "2016-06-24" @default.
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• W2418106836 date "2011-06-07" @default.
• W2418106836 modified "2023-10-16" @default.
• W2418106836 title "Efficient and Regioselective 9-<i>Endo</i> Cyclization of α-Carbamoyl Radicals" @default.
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• W2418106836 doi "https://doi.org/10.1021/ol201180g" @default.
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