Direct -Me Aziridination of Enones
Overview
Overview
Journal
J Org Chem
Publisher
American Chemical Society
Specialty
Chemistry
Date
2022 Feb 16
PMID
35171590
Authors
Affiliations
Affiliations
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Abstract
The first direct general method for Me aziridination of electron-deficient olefins, enones, is described using -methyl--tosylhydroxylamine as the aminating agent in the presence of a Cu(OTf) catalyst. The aziridination of vinyl ketones, hitherto unknown for -Me as well as -H, has been achieved efficiently. The open-flask reaction is stereospecific, operationally simple, and additive-free. It also efficiently affords -H aziridinated products under a similar reaction condition.