4.6 Article

Organocatalyzed aza-Michael-Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers

期刊

RSC ADVANCES
卷 3, 期 38, 页码 16999-17002

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ra42783h

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资金

  1. National Basic Research Program of China (973 Program) [2010CB833200]
  2. National Natural Science Foundation of China [20172064, 203900502, 20532040]
  3. Shanghai Natural Science Council
  4. Excellent Foundation of China (Young Scholars Foundation of National Natural Science) [20525208]

向作者/读者索取更多资源

An efficient organocatalytic aza-Michael-Michael cascade reaction for the asymmetric synthesis of highly functionalized spirooxindole tetrahydroquinolines has been reported through a formal [4+2] annulation strategy.

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