Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Literature Information
Lu Song
We reported herein a simple and efficient visible-light promoted intermolecular haloamination and haloetherification of alkenes using N-halosaccharin as the halogen and nitrogen/oxygen source (halo = Br, Cl). The reaction can be applied to a very broad range of alkenes to generate haloamines and haloethers with high isolated yields. With DBU as the base, metal-free C–H amination of aryl olefins has also been achieved with good yields.
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
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