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- W2944556711 abstract "Diastereoselective α-amination of N-tert-butanesulfinyl imidates has been developed using N-aryl (or N-tert-butyl) N-diphenylphosphinyldiazenes as nitrogen sources. The chiral 1-azaenolates derived from imidates undergo nucleophilic addition with diazenes to give α-hydrazino imidates in good yields." @default.
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- W2944556711 date "2019-05-09" @default.
- W2944556711 modified "2023-10-17" @default.
- W2944556711 title "Diastereoselective α-Amination of <i>N</i>-<i>tert</i>-Butanesulfinyl Imidates Using <i>N</i>-Aryl-<i>N</i>-diphenylphosphinyldiazenes" @default.
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- W2944556711 doi "https://doi.org/10.1021/acs.joc.9b00877" @default.
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