Background

Chapter
Part of the Springer Theses book series (Springer Theses)

Abstract

For a long time, the realm of asymmetric catalysis was dominated by metal and biocatalysis. Yet, at the beginning of this century, List’s discovery of the (S)-proline-catalyzed direct asymmetric intermolecular aldol reaction [1] together with the development of an asymmetric Diels–Alder reaction catalyzed by a chiral imidazolidinone salt by MacMillan et al. [2] have raised awareness of the potential of purely organic molecules as efficient catalysts for a variety of asymmetric transformations and brought to life the term “organocatalysis” to address this research field (Scheme 2.1).

Keywords

High Enantioselectivities Alkaline Hydrogen Peroxide Conjugate Addition Cinchona Alkaloid Asymmetric Epoxidation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  1. 1.Max-Planck-Institut für KohlenforschungMülheim an der RuhrGermany

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