| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6506205 | Chinese Journal of Catalysis | 2016 | 7 Pages |
Abstract
A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C-H activation process. Starting from readily available N-sulfinyl imine substrates and alkynes, the reaction occurred via N-S cleavage with broad substrate scope and functional group compatibility in the presence of a cost-effective cobalt catalyst.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Fen Wang, Qiang Wang, Ming Bao, Xingwei Li,