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• W1754095384 startingPage "6930" @default.
• W1754095384 abstract "A number of structurally and electronically diverse N-vinyl nitrones have been synthesized by a two-step method. The sequence consists of condensation of an α-chloroaldehyde or an α-phenoxy- or α-acetoxy ketone with a substituted benzyl hydroxylamine to provide the corresponding nitrone. Treatment of these species with a base induces a 1,4-elimination to provide the desired N-vinyl nitrone in good to excellent yields." @default.
• W1754095384 created "2016-06-24" @default.
• W1754095384 creator A5042902371 @default.
• W1754095384 creator A5045432540 @default.
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• W1754095384 date "2015-06-16" @default.
• W1754095384 modified "2023-10-17" @default.
• W1754095384 title "Synthesis of <i>N</i>-Vinyl Nitrones via 1,4-Conjugate Elimination" @default.
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• W1754095384 doi "https://doi.org/10.1021/acs.joc.5b01138" @default.
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