| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269054 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
A rhodium-catalyzed asymmetric 1,2-additions of arylboronic acids to isatins with chiral sulfur-alkene hybrid ligands was achieved, and a variety of 3-aryl-3-hydroxy-2-oxindoles were obtained in moderate to good yields with up to 85% ee. And a biologically active compound was synthesized with this strategy.63
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiangqing Feng, Yanzhao Nie, Lanqiong Zhang, Jing Yang, Haifeng Du,