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Enantioselective Synthesis of Arene cis-Dihydrodiols from 2-Pyrones.

Xiao-Wei LiangYunlong ZhaoXu-Ge SiMeng-Meng XuJia-Hao TanZhi-Mao ZhangCheng-Gong ZhengChao ZhengQuan Cai
Published in: Angewandte Chemie (International ed. in English) (2019)
An enantioselective chemical synthesis of arene cis-dihydrodiols has been realized from 2-pyrones through sequential ytterbium-catalyzed asymmetric inverse-electron-demand Diels-Alder (IEDDA) reaction of 2-pyrones and retro-Diels-Alder extrusion of CO2 . By using this strategy, a series of substituted arene cis-dihydrodiols can be obtained efficiently with high enantioselectivity (>99 % ee in many cases). Based on this strategy, efficient and concise asymmetric total syntheses of (+)-MK7607 and 1-epi-(+)-MK7607 were accomplished.
Keyphrases
  • water soluble
  • molecular docking
  • room temperature
  • molecular dynamics simulations