| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218197 | Tetrahedron | 2013 | 6 Pages |
Abstract
The first application of 4-nitrophthalimide as nitrogen nucleophile for enantioselective aza-Michael addition to nitroalkenes has been developed. The process is promoted by chiral thiourea catalyst derived from cinchonine to give corresponding Michael adducts with up to 87% ee. Activity test showed that some products of the reaction have moderate or good herbicidal activity against cole and barnyard grass at 100 μg/ml.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shijun Ma, Lulu Wu, Ming Liu, Yaodong Huang, Yongmei Wang,