The highly enantioselective catalytic aza-Morita–Baylis–Hillman reaction

Literature Information

Publication Date 2014-03-13
DOI 10.1039/C4QO00026A
Impact Factor 5.281
Authors

Fang-Le Hu, Min Shi



Abstract

The highly enantioselective aza-Morita–Baylis–Hillman (aza-MBH) reaction is one of the most important reactions for the synthesis of optically active α-methylene-β-amino carbonyl compounds. The use of chiral phosphines or amines as organocatalysts can be envisaged for this catalytic asymmetric reaction. This mini review focuses on the important developments with regard to asymmetric aza-MBH reactions catalyzed by chiral phosphines or amines or even organometallic complexes in recent decades and also on the perspectives that these new developments offer.

Source Journal

Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
Self-citation Rate: 8.7%
Articles per Year: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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