The enantioselective Morita-Baylis-Hillman reaction and its aza counterpart |
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Authors: | Masson Géraldine Housseman Christopher Zhu Jieping |
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Affiliation: | Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette Cedex, France. Geraldine.Masson@icsn.cnrs-gif.fr |
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Abstract: | The development of asymmetric Morita-Baylis-Hillman (MBH) reactions has evolved dramatically over the past few years, parallel to the emerging concept of bifunctional organocatalysis. Whereas organocatalysis is starting to compete with metal-based catalysis in several important organic transformations, the MBH reaction belongs to a group of prototypical reactions in which organocatalysts already display superiority over their metal-based counterparts. This Minireview summarizes recent mechanistic insights and advances in the design and synthesis of small organic molecules for enantioselective MBH and aza-MBH reactions. |
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Keywords: | asymmetric synthesis Brønsted acids Lewis bases organocatalysis reaction mechanisms |
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