Article ID Journal Published Year Pages File Type
5275956 Tetrahedron Letters 2007 4 Pages PDF
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
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