Chinese Journal of Magnetic Resonance

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STRUCTURE ELUCIDATION OF SESQUITERPENOIDES FROM ELEPHANTOPUS SCABER USING THE NOESY TECHNIQUE  (I)

LIANG Qiao-li1,2,SHI Guo-xin1   

  1. 1.Nanjing Normal University, Nanjing 210097, China; 2.Nanjing University of Traditional Chinese Medicine, Nanjing 200029, China
  • Received:2003-01-09 Revised:2003-03-24 Published:2003-09-05 Online:2003-09-05
  • Supported by:

    国家自然科学基金资助项目(39670089).

Abstract:

Objective To determine the C-2 conformation of two pair of stereo-isomers of germacranolide type, which are scabertopin and isoscabertopin, isodeoxyel
ephantopin and deoxyelephantopin isolated from Elephantopus scaber. Methods The NOESY technique was used along with 1H NMR,13C NMR and HMQC. Results The differences between the NOESY spectra of the two pairs of stereo-isomers were found. Conclusion The C-2 conformation of the two pairs of stereo-isomers from Elephantopus scaber can be determined through the NOESY technique.

Key words: NMR, NOESY, Elephantopus scaber, sesquiterpenoides, scabertopin, deoxyelephantopin

CLC Number: