Journal
GREEN CHEMISTRY
Volume 23, Issue 7, Pages 2624-2627Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0gc03899g
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A transition metal-free synthesis of N-(arylthio/seleno)ethyl sulfoxidmines was achieved via blue light-promoted radical sulfoximido-chalcogenization of aliphatic and aromatic alkenes. The sulfoximidation process exhibited high chemoselectivity and broad substrate scope, providing good yields in the sulfoximido-chalcogenization of alkenes.
A transition metal-free synthesis of N-(arylthio/seleno)ethyl sulfoxidmines via blue light-promoted radical sulfoximido-chalcogenization of aliphatic and aromatic alkenes was developed. The sulfoximidation process demonstrated high chemoselectivity and allowed a broad substrate scope, completing the sulfoximido-chalcogenization of alkenes in good yields.
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