| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 59330 | Chinese Journal of Catalysis | 2015 | 8 Pages |
Abstract
A facile Pd-catalyzed intramolecular aminofluorination reaction of allylic sulfamides was developed that can be used to prepare fluorinated 1,3-diamine derivatives. Acetic acid was essential for regulation to give the major 6-endo cyclization products.
Graphical AbstractA facile Pd-catalyzed intramolecular aminofluorination reaction of unactivated alkenes was developed that can be used to prepare fluorinated 1,3-diamine derivatives.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Jiashun Cheng, Pinhong Chen, Guosheng Liu,