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3-(Methoxycarbonyl)Cyclobutenone as a Reactive Dienophile in Enantioselective Diels-Alder Reactions Catalyzed by Chiral Oxazaborolidinium Ions.

Peng YanChangxu ZhongJie ZhangYu LiuHuayi FangPing Lu
Published in: Angewandte Chemie (International ed. in English) (2021)
Cyclobutenone has been used as a highly reactive dienophile in Diels-Alder reactions, however, no enantioselective example has been reported. We disclose herein a chiral oxazaborolidine-aluminum bromide catalyzed enantioselective Diels-Alder reaction of 3-alkoxycarbonyl cyclobutenone with a variety of dienes. Furthermore, a total synthesis of (-)-kingianin F was completed for the first time via enantioenriched cycloadduct bicyclo[4.2.0]octane derivative.
Keyphrases
  • room temperature
  • ionic liquid
  • capillary electrophoresis
  • quantum dots
  • water soluble