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- W2785163826 abstract "A photoredox catalytic approach to synthetically valuable N-acyl-N'-aryl-N,N'-aminals is described. This method uses the addition of a radical precursor to enamides, with subsequent interception of the cationic iminium intermediate with an arylamine. The reaction has been shown to be compatible with electron-rich and electron-deficient arylamines, and moderate to good levels of diastereoselectivity can be attained using a chiral enamide. Furthermore, the N-acyl-N'-aryl-N,N'-aminal reaction products can be readily cyclized, providing a novel synthetic route to valuable γ-lactams." @default.
- W2785163826 created "2018-02-02" @default.
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- W2785163826 date "2018-01-26" @default.
- W2785163826 modified "2023-09-27" @default.
- W2785163826 title "Photoredox Approach to <i>N</i>-Acyl-<i>N′</i>-aryl-<i>N</i>,<i>N′</i>-aminals Using Enamides and Their Conversion to γ-Lactams" @default.
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- W2785163826 doi "https://doi.org/10.1021/acs.orglett.7b03946" @default.
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