Regioselective 1,2-additions of alcohols to allenamides mediated by N-Iodosuccinimide: Synthesis of N,O-aminals
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Add time:07/19/2019 Source:sciencedirect.com
N,O-Aminals are synthesized through the N-iodosuccinimide-mediated regioselective 1,2-additions of alcohols to allenamides. These novel reactions proceed rapidly and exhibit broad substrate scope for a variety of allenamides. The reaction demonstrates that N-Iodosuccinimide is effective in activating the terminal CC bond of allenamides generating conjugated sulfamide ion species. It is noteworthy that the alcohol served as both solvent and nucleophile in this transformation.
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