Journal of Jilin University Science Edition ›› 2019, Vol. 57 ›› Issue (06): 1530-1534.

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Chiral Separation of Enantiomer of 2-Oxabicyclo[3,3,0]oct-6-en-3-oneand Determination of Optical Purity#br#

CAO Hong1,2, WANG Shuhong3, ZHAO Chunying3, HU Chuanmin1, CAI Jianhui1, XIU Zhiming1   

  1. 1. Jilin Collaborative Innovation Center for Antibody Engineering, Jilin Medical University, Jilin 132013, Jilin Province, China; 2. The ChinaJapan Union Hospital of Jilin University, Changchun 130021, China;3. Changchun BC&HC Pharmaceutical Technology Co., Ltd, Changchun 130012, China
  • Received:2019-08-02 Online:2019-11-26 Published:2019-11-21
  • Contact: XIU Zhiming E-mail:Xiuzm10@mails.jlu.edu.cn

Abstract: The chiral silicon surface coated with cellulosethree (3,5dimethylphenyl carbamate) was used as stationary phase, the solvent of  V(nhexane)∶V(isopropyl alcohol)=95∶5 was used as mobilephase to  separate  2-oxabicyclo[3,3,0]oct-6-en-3-one. The flow rate  was 08 mL/min, the column temperature was 25 ℃, and detection wavelength was 205 nm. The results show that the resolution is 3.0, the enantiomer can be effectively separated, and the optical purity can be determined by area normalization method.

Key words: 2-oxabicyclo[3,3,0]oct-6-en-3-one, enantiomer, separation, optical purity

CLC Number: 

  • O641.6