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Asymmetric Bromoaminocyclization and Desymmetrization of Cyclohexa-1,4-dienes through Anion Phase-Transfer Catalysis.

Hai-Jiao LongYin-Long LiBing-Qian ZhangWen-Ying XiaoXiao-Ying ZhangLing HeJun Deng
Published in: Organic letters (2021)
The catalytic enantioselective desymmetrizing bromoaminocyclization of prochiral cyclohexa-1,4-dienes has been achieved by using chiral anion phase-transfer catalysis, providing a range of enantioenriched cis-3a-arylhydroindoles bearing an all-carbon quaternary stereocenter in good yields (up to 78%) and excellent enantioselectivities (up to 97% ee). Furthermore, the potential application of this methodology to natural product total synthesis was demonstrated by the asymmetric synthesis of (+)-Mesembrane.
Keyphrases
  • ionic liquid
  • visible light
  • mass spectrometry
  • climate change