Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfonesviaenamine activation

Literature Information

Publication Date 2007-03-21
DOI 10.1039/B701216K
Impact Factor 6.222
Authors

Sarah Sulzer-Mossé, Alexandre Alexakis


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Abstract

Over the last decade the potential of organocatalysis has successfully been demonstrated. In particular, chiral amines such as pyrrolidine analogues have emerged as a broadly applicable class of organocatalyst for asymmetric conjugate addition viaenamine activation. This Feature Article documents the development of these catalysts, emphasizing the design and mechanistic features that supply high selectivity in asymmetric Michael reactions.

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Chemical Communications

Chemical Communications
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