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Asymmetric Cycloaddition of ortho-Hydroxyphenyl-Substituted para-Quinone Methides and Enamides Catalyzed by Chiral Phosphoric Acid.

Guo-Hui YangQun ZhaoZhi-Pei ZhangHan-Liang ZhengLi ChenXin Li
Published in: The Journal of organic chemistry (2019)
A BINOL-based chiral phosphoric acid was employed as an efficient catalyst in enantioselective cycloaddition of ortho-hydroxyphenyl-substituted para-quinone methides and enamides, which gave rise to acetamido-substituted tetrahydroxanthenes with three adjacent stereogenic centers in high yields (up to 99%) and excellent stereoselectivities (up to >99:1 diastereomeric ratio and up to 98% ee).
Keyphrases
  • molecular docking
  • ionic liquid
  • room temperature
  • capillary electrophoresis
  • molecular dynamics simulations
  • reduced graphene oxide