Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275956 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Catalytic highly enantioselective (up to >99% ee) and diastereoselective (up to 99% de) direct Michael addition of ketones and aldehydes to β-nitrostyrenes have been achieved with readily accessible and highly tunable prolinal dithioacetal catalysts.
Graphical abstractHigh enantioselectivity and diastereoselectivity has been achieved in the direct Michael addition with readily tunable prolinal dithioacetal catalysts.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tanmay Mandal, Cong-Gui Zhao,