Abstract
Functionalized arylmagnesium compounds prepared via a halogen-magnesium exchange reaction using aryl iodides or bromides and i-PrMgCl·LiCl, react rapidly with benzyl-N-chloroamines at -45 °C providing polyfunctional tertiary amines in good yields. The methodology is also successfully applied to the preparation ofchiral N-chloroamines with retention ofchirality.
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