| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276538 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Catalytic enantioselective Michael addition reactions of α-amino functionalized aldehydes to nitroolefins have been developed. The Michael product was obtained in up to 98% ee, but the enantiomeric purity of the Michael product was decreased during isolation of the product.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Klaus Albertshofer, Rajeswari Thayumanavan, Naoto Utsumi, Fujie Tanaka, Carlos F. III,