Chinese Journal of Magnetic Resonance ›› 2009, Vol. 26 ›› Issue (2): 239-246.

• Articles • Previous Articles     Next Articles

Synthesis and NMR Studies of a Novel Chrysin-7-yl Phosphoramidate Derivative

CHEN Xiao-lan1; ZHANG Shou-ren1; QU Ling-bo1,2*; YUAN Jin-wei1; ZHOU Ya-dong1; LIU Nai-fang1; ZHAO Yu-fen1,3   

  1. (1.Key Laboratory of Chemical Biology and Organic Chemistry, Department of Chemistry, Zhengzhou University, Zhengzhou 450052, China; 2.School of Chemistry & Chemical Engineering, Henan University of Technology,
    Zhengzhou 450052, China; 3.Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China)
  • Received:2008-11-10 Revised:2008-11-27 Online:2009-06-05 Published:2009-12-05
  • Contact: QU Ling-bo

Abstract: In this study, the phosphorylated glycine methyl ester was coupled with chrysin to form a novel chrysin-7-yl phosphoramidate derivative by a facile phosphorylated reaction. Complete assignment of the 1H and 13C NMR chemical shifts of the synthesized compound was obtained by 2D NMR techniques, including DEPT, 1H-1H COSY, 13C-1H HSQC and 13C-1H HMBC. ESI MS/MS spectra of the compound were also recorded and used to study its fragmentation behaviors.

Key words: NMR, assignment, 2D NMR, chrysin, phosphoramidate

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