Chinese Journal of Magnetic Resonance ›› 2007, Vol. 24 ›› Issue (1): 85-90.

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The Phosphorylation Reaction between Daidzein and Di-isopropyl Phosphite Studied by NMR and ESI-MS/MS

CHEN Xiao-lan1*;SHI Xiao-na1;QU Ling-bo1;YUAN Jin-wei1;LU Jian-sha1;ZHAO Yu-fen1,2   

  1. (1.Key Laboratory of Chemical Biology Department of Chemistry, Zhengzhou University, Zhengzhou 450052, China; 2.The Key Laboratory for Bioorganic Phosphorus Chemistry & Chemical Biology (Tsinghua University), Ministry of Education, Beijing 100084, China)
  • Received:2006-03-01 Revised:2006-08-17 Published:2007-03-05 Online:2009-12-05
  • Contact: Chen Xiao-lan

Abstract: The Atheron-Todd reaction has been used extensively for synthesis of phosphates and phosphoroamidates. In this study, we showed that daidzein can be phosphorylated by a modified Atheron-Todd procedure in which dialkyl phosphite and tetrachloromethane mixture was dropped into a mixed solution of daidzein, trithylamine and DMF. The reaction product was obtained with good yield, whose structure was determined by NMR, ESI-MS and X-ray crystallography.

Key words: NMR, ESI-MS, daidzein, phosphorylation, X-ray crystallography

CLC Number: