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.
Original language | English |
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Pages (from-to) | 2862-2867 |
Number of pages | 6 |
Journal | Molecules |
Volume | 14 |
Issue number | 8 |
DOIs | |
Publication status | Published - Aug 2009 |
Scopus Subject Areas
- Analytical Chemistry
- Chemistry (miscellaneous)
- Molecular Medicine
- Pharmaceutical Science
- Drug Discovery
- Physical and Theoretical Chemistry
- Organic Chemistry
User-Defined Keywords
- Daucus carot
- Sesquiterpene
- Umbelliferae