| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5272043 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The first expeditious nitroaziridination of N-tosylaldimines is reported. The protocol involves operationally simple catalyst-free reaction of N-tosylaldimines, 1-bromonitroalkanes and NaOAc to afford 2-nitro-1-tosylaziridines in excellent yields with high Z-diastereoselectivity in a one-pot procedure under ambient conditions.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lal Dhar S. Yadav, Garima Garima, Ritu Kapoor,