Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218467 | Tetrahedron | 2013 | 7 Pages |
Abstract
A new method has been developed for the asymmetric oxaziridination of aryl aldimines with m-chloroperbenzoic acid, involving the use of cinchona alkaloid derivatives containing a sulfide moiety as a catalyst. The new method provided access to optically active oxaziridines in good yields with high enantiomeric excess (ee) values of up to 95%.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tianyi Zhang, Wei He, Xingyu Zhao, Ying Jin,