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Abstract
A novel dimeric sesquiterpene having a C 2-symmetric structure was isolated from the roots of Chloranthus serratus. The unique cyclic structure, including a 12-membered ring, was elucidated principally by 1D- and 2D-NMR methods and the stereochemistry was disclosed through detecting NOEs between equivalent protons by 13C-coupled HMQC-NOESY.
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