Citation: Zhu Qingying, Shen Haimin, Ji Hongbing. Asymmetric Epoxidation of trans-Chalcone by H2O2 Induced by β-Cyclodextrin Derivatives in Water[J]. Chinese Journal of Organic Chemistry, ;2016, 36(8): 1907-1914. doi: 10.6023/cjoc201512022 shu

Asymmetric Epoxidation of trans-Chalcone by H2O2 Induced by β-Cyclodextrin Derivatives in Water

  • Corresponding author: Ji Hongbing, jihb@mail.sysu.edu.cn
  • Received Date: 17 December 2015
    Revised Date: 19 February 2016

    Fund Project: Project supported by the National Science Fund for Distinguished Young Scholars No. 21425627

Figures(6)

  • Six amino-alcohol modified β-cyclodextrins CD-1~CD-6 were synthesized by nucleophilic substitution from mono(6-O-p-tolylsulfonyl)-β-cyclodextrin with the yields of 34%~58%, and were verified by 1H NMR, 13C NMR and ESI-MS techniques. These β-cyclodextrin derivatives were applied to the asymmetric epoxidation of trans-chalcone by H2O2. And the results implied that the dosage of the β-cyclodextrin derivatives and the structure of the modified group had an important effect on the enantioselectivity in the reaction. Among them, CD-1 exhibited the best performance in the asymmetric epoxidation of trans-chalcone employed H2O2 and NaHCO3 as oxidant, and 25.7% ee value was obtained. It were showed from the spectra of 2D-1H ROESY NMR that, CD-1 could form inclusion complex with trans-chalcone and self-inclusion existed in all the β-cyclodextrin derivatives CD-1~CD-6, which affected the enhancement of the ee value. And the two kinds of inclusion complexes were confirmed by quantum chemistry calculation too.
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