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Catalytic Enantioselective Synthesis of 2,5-Dihydrooxepines.

Su Yong ShimSoo Min ChoAnipireddy VenkateswarluDo Hyun Ryu
Published in: Angewandte Chemie (International ed. in English) (2017)
A Michael addition initiated cyclopropanation/retro-Claisen rearrangement tandem reaction was developed for the enantioselective synthesis of highly functionalized 2,5-dihydrooxepines. In the presence of a chiral oxazaborolidinium ion (COBI) catalyst, the reaction proceeds to give good yields and high enantioselectivity.
Keyphrases
  • ionic liquid
  • room temperature
  • quantum dots
  • highly efficient
  • carbon dioxide
  • mass spectrometry
  • capillary electrophoresis
  • metal organic framework