Abstract
Aziridination of a variety of alkenes with N-substituted hydrazines mediated by iodobenzene diacetate under mild conditions (K 2CO 3, CH 2Cl 2) and ambient temperature were achieved in good to excellent yields (up to 99%), and conversions. The practicality and simplicity of this C–N bond formation protocol was exemplified by its application to the aziridination of cholesteryl acetate in a stereoselective manner.
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