Abstract
Further study on the sesquiterpenes from Curcuma aromatica (Zngiberaceae) has resulted in the isolation of eleven minor sesquiterpenes, 1-11 having guaiane, seco-guaiane and germacrane skeletons, and their structures were elucidated by proton nuclear magnetic resonance (1H-NMR) and 13C-nuclear magnetic resonance (13C-NMR) spectroscopy, as well as chemical investigation. The stereochemistry of these sesquiterpenes was elucidated by 2D NMR techniques such as 1H-H correlation (COSY) and nuclear Overhauser effect correlation (NOESY), and circular dichroism (CD) spectroscopy.