| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5262273 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
A novel arylnitration of alkenes by nitration and C-H functionalization cascade process has been developed. This methodology provides an efficient way to construct a variety of nitro-containing oxindoles and dihydroquinolin-2(1H)-ones. In addition, the process exhibits significant functional group tolerance. Moreover, the use of inexpensive and readily available starting materials makes this practical and atom-economical approach particularly attractive.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ya-Min Li, Yuehai Shen, Kwen-Jen Chang, Shang-Dong Yang,