Abstract
Phytochemical investigation of the fruits of Daucus carota L. resulted in the isolation of a new sesquiterpene named as daucucarotol (1). Its structure was elucidated on the basis of 1D and 2D NMR experiments, coupled with MS studies. To our knowledge, compound 1 is the first example for a natural eudesmane sesquiterpene with a hydroxymethyl group located at a methine carbon rather than a usual quaternary carbon in the two fused six-membered ring systems. © 2008.
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Fu, H. W., Zhang, L., Yi, T., & Tian, J. K. (2009). A new sesquiterpene from the fruits of daucus carota L. Molecules, 14(8), 2862–2867. https://doi.org/10.3390/molecules14082862
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