| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1345068 | Tetrahedron: Asymmetry | 2008 | 6 Pages |
Abstract
Ring opening of meso-aziridines with benzenethiols utilizing quinine as an organocatalyst has been developed. The reaction proceeded smoothly in the presence of 10 mol % of quinine in CHCl3 to afford β-amino sulfides in high yields and with moderate to good enantioselectivities.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Zhiyong Wang, Xiaoyu Sun, Shengqing Ye, Weizi Wang, Bing Wang, Jie Wu,