4.7 Article

Enantioselective Michael addition of ketones to maleimides catalyzed by bifunctional monosulfonyl DPEN salt

期刊

CHEMICAL COMMUNICATIONS
卷 46, 期 25, 页码 4589-4591

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc00774a

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资金

  1. Shanghai Pujiang Program [08PJ1403300]
  2. National Natural Science Foundation of China [20902018]
  3. Fundamental Research Funds for the Central Universities

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An unprecedented enantioselective Michael addition of various ketones to maleimides catalyzed by a simple bifunctional primary amine, monosulfonyl DPEN salt, is reported and provides the desired adducts in good to excellent yields (up to 99%) with excellent enantioselectivities (up to 99%).

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