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Organocatalytic Asymmetric Aza‐Michael Additions

Chemistry - A European Journal · 2009 · Vol. 15(42) · pp. 11058–11076
Dieter EndersChuan WangJens Liebich

Abstract

The catalytic aza-Michael addition is an important reaction within synthetic organic chemistry, given the significance of the biologically and synthetically interesting products, such as beta-amino acids and beta-lactams. In the last decade organocatalysis emerged as a powerful tool in asymmetric synthesis and had a large impact on the development of asymmetric and catalytic conjugate additions of nitrogen nucleophiles to Michael acceptors. In this review a first summary of the recent rapid progress of asymmetric organocatalyzed aza-Michael reactions is presented.

Asymmetric Synthesis and CatalysisSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and CatalysisMichael reactionOrganocatalysisNucleophileConjugateEnantioselective synthesisChemistryCatalysisOrganic synthesisAddition reactionOrganic chemistry
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References
Organocatalytic Synthesis of Drugs and Bioactive Natural Products
European Journal of Organic Chemistry · 2007 · 369 citations
Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions
European Journal of Organic Chemistry · 2007 · 1,145 citations
The Phospha‐Michael Addition in Organic Synthesis
European Journal of Organic Chemistry · 2005 · 336 citations
Enantioselective Conjugate Additions
Tetrahedron · 2000 · 810 citations
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