Chinese Journal of Magnetic Resonance ›› 2004, Vol. 21 ›› Issue (2): 249-261.

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ANALYSIS OF THE CONFIGURATION AND CONFORMATION OF GERMACRANE TYPE SESQUITERPENOIDS

 GAO Kun,  Li-Xin   

  1. College of Chemistry and Chemical Engineering, National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000,  China
  • Received:2003-10-28 Revised:2003-12-03 Online:2004-06-05 Published:2004-06-05
  • Supported by:

    国家自然科学基金“有机化学创新群体基金”(20021001)和面上基金(20372029)资助项目.

Abstract:

Germacrane type sesquiterpenoids are the most abundant among all the sesquiterpenoid skeletons. Their stereostructures vary much because of the decacycle. There are four configurational isomers and every configuration has several different conformers of germacrane derivatives, which tend to exist as the most stable conformers. All these conclusions are established by NMR spectroscopic techniques, including dynamics NMR (DNMR), NOED and NOESY, etc. These four configurational isomers and their relatively stable conformers are summarized by analyzing NMR spectral data in this article.

Key words: NMR, configuration, conformation, sesquiterpenoid, germacrane

CLC Number: