| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278016 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
Novel rearrangement was found by reacting anilines with HCHO/H2O2 resulting in the synthesis of various benzaldoximes. The mechanism of the rearrangement is proposed and suggested that the rearrangement might proceed via unstable N-phenyloxazirane intermediate followed by the transfer of aryl moiety from nitrogen to carbon atom leading to the formation of benzaldoxime.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naval Kapuriya, Kalpana Kapuriya, Narsinh M. Dodia, Yi-Wen Lin, Rajesh Kakadiya, Chao-Ting Wu, Ching-Huang Chen, Yogesh Naliapara, Tsann-Long Su,