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Novel total syntheses of oxoaporphine alkaloids enabled by mild Cu-catalyzed tandem oxidation/aromatization of 1-Bn-DHIQs.

Bo ZhengHui-Ya QuTian-Zhuo MengXia LuJie ZhengYun-Gang HeQi-Qi FanXiao-Xin Shi
Published in: RSC advances (2018)
Novel total syntheses of oxoaporphine alkaloids such as liriodenine, dicentrinone, cassameridine, lysicamine, oxoglaucine and O -methylmoschatoline were developed. The key step of these total syntheses is Cu-catalyzed conversion of 1-benzyl-3,4-dihydro-isoquinolines (1-Bn-DHIQs) to 1-benzoyl-isoquinolines (1-Bz-IQs) via tandem oxidation/aromatization. This novel Cu-catalyzed conversion has been studied in detail, and was successfully used for constructing the 1-Bz-IQ core.
Keyphrases
  • room temperature
  • hydrogen peroxide
  • aqueous solution
  • metal organic framework
  • nitric oxide