| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5213839 | Tetrahedron | 2016 | 7 Pages |
Abstract
A series of chiral ferrocenyl P,S-ligands based on benzimidazole and imidazole backbones have been prepared from Ugi's amine through a three-step transformation. These ligands were successfully employed in the Cu-catalyzed asymmetric [3+2] cycloaddition of azomethine ylides with various electron-deficient olefins, giving the corresponding cycloadducts in high endo-selectivities and excellent enantioselectivities (up to 99% ee).
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Fu-Zhong Han, Sai-Bo Yu, Cheng Zhang, Xiang-Ping Hu,
![First Page Preview: Chiral ferrocenyl P,S-ligands for highly efficient copper-catalyzed asymmetric [3+2] cycloaddition of azomethine ylides Chiral ferrocenyl P,S-ligands for highly efficient copper-catalyzed asymmetric [3+2] cycloaddition of azomethine ylides](/preview/png/5213839.png)