Enantioselective Organocatalytic Conjugate Addition of N Heterocycles to α,β-Unsaturated Aldehydes.
✍ Scribed by Peter Diner; Martin Nielsen; Mauro Marigo; Karl Anker Joergensen
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 32 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Organocatalysis [1] has expanded widely within the last few years, since the rediscovery of the proline-catalyzed aldol reaction. [2] Since then, several different methods, such as fluorination, [3] chlorination, [4] bromination, [5] sulfenylation, [6] amination, [7] and Mannich reactions, [8] have
## Abstract The first example of an organocatalytic asymmetric Michael addition of aldehydes to α,β‐unsaturated thiol esters promoted by chiral diphenylprolinol silyl ether is presented. The reaction occurs with good yields, diastereoselectivity and excellent enantioselectivity.