Chinese Journal of Magnetic Resonance ›› 1991, Vol. 8 ›› Issue (1): 19-28.

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APPLICATION OF NOE AND 2D NMR SPECTROSCOPY TO THE ASSIGNMENT OF 1H AND 13C CHEMICAL SHIFTS IN SESQUI-TERPENOIDS

Sang Hong1, Wang Hanging1, Tu Yongqiang2   

  1. 1. Lanzhou Institute of Chemical Physics, Academia Sciences, Lanzhou, Gansu, P. R. China;
    2. Deportment of Chemistry, Lanzhou University, Lanzhou, Gansu, P. R. China
  • Received:1989-12-25 Revised:1990-04-28 Published:1991-03-05 Online:2018-01-20

Abstract: The stereochcmical and structural analysis of two sesquiterpenoids was carried out using nuclear magnetic resonance spectroscopy. Several methods, including 1H-1H two-dimensional shift correlation spectroscopy, 13C-1H two-dimensional shift correlation spectroscopy, COLOC (COrrelation spectroscopy via LOng range Coupling), DEPT (Distortionless Enhancement by Polarization Transfer) were used for chemical shift assignment and configurational analysis. Nuclear Overhauser Effect Spectroscopy was used to establish the stereochemistry. This investigation demonstrates the power of two-dimensional NMR techniques and the Nuclear Overhauser Effect (NOE) in the structural determination of natural products.

Key words: Sesquiterpenoid, 2D NMR, NOE