| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7753006 | Journal of Fluorine Chemistry | 2015 | 18 Pages |
Abstract
A highly diastereoselective reductive amination of ketones using 2-chloro-1,1,2,2-tetrafluoroethane-1-sulfinamide as auxiliary was developed. Both aromatic and aliphatic ketones reacted well under the reaction conditions, giving the corresponding amination products in good yields with excellent diastereoselectivities.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Kai Yang, Jin-Tao Liu,