4.7 Article

Aminocatalytic asymmetric inverse-electron-demand aza-Diels-Alder reaction of N-Ts-1-aza-1,3-butadienes based on coumarin cores

期刊

CHEMICAL COMMUNICATIONS
卷 46, 期 15, 页码 2665-2667

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/b925424b

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资金

  1. National Natural Science Foundation of China [20972101]
  2. PCSIRTC [IRT0846]
  3. National Basic Research Program of China (973 Program) [2010CB833303]

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The asymmetric inverse-electron-demand aza-Diels-Alder reaction of N-Ts-1-aza-1,3-butadienes derived from 3-argiocarbonyl-coumarins and acetaldehyde has been developed using chiral secondary aminocatalysis, giving tricyclic chroman-2-one derivatives in high enantioselectivities (up to 95% ee).

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