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Journal Article

The ying and yang of asymmetric aminocatalysis


List,  Benjamin
Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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List, B. (2006). The ying and yang of asymmetric aminocatalysis. Chemical Communications, 2006(8), 819-824. doi:10.1039/b514296m.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-A46E-2
During the last six years the asymmetric catalysis of carbonyl transformations via iminium ion and enamine intermediates using chiral amines as organocatalysts has grown most remarkably. In this personal account an overview of this area is given. The field can be divided into two sub areas: (a) Iminium catalysis, which is typically used for cycloadditions and conjugate additions to enals and enones and (b) Enamine catalysis, which is commonly used in electrophilic α-substitution reactions of ketones and aldehydes. A common origin of the two catalysis principles is proposed and their recent merger in tandem sequences is discussed.