| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219994 | Tetrahedron | 2012 | 7 Pages |
Abstract
A series of fluorinated N-aminoaziridines have been synthesized by the PhI(OAc)2-mediated aziridination procedure. The reaction was carried out with various protected hydrazides and fluorinated alkenes. The reaction was extended to alkenes bearing an amino acid and the ring opening of the CF3-N-aminoaziridines has been investigated.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bertrand Schweitzer-Chaput, Massaba Keita, Thierry Milcent, Sandrine Ongeri, Benoit Crousse,