Abstract
The development of the first intermolecular Rh2(II)-catalyzed aziridination of di-, tri-, or tetraubstituted olefins using aryl- or heteroaryl amines as nonactivated N-atom precursors and an iodine(III) reagent as the stoichiometric oxidant is reported. The Rh2(II)-catalyzed N-atom transfer to the olefin is stereospecific, chemo- and diastereoselective to produce the N-aryl aziridine as the only amination product.
Supplementary materials
Title
aziridine 15p
Description
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Title
aziridine 15l
Description
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Title
SI aziridination
Description
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