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1.
Z Naturforsch C J Biosci ; 55(5-6): 318-22, 2000.
Article in English | MEDLINE | ID: mdl-10928539

ABSTRACT

The exudate of Ozothamnus hookeri has been investigated for its non-flavonoid constituents. A new natural C6-C3 ester of a long chain fatty acid and seven structurally related kaurane-diterpenoids were isolated. Three of the latter are new natural products, too. A rare 8-methoxy flavonol was also identified.


Subject(s)
Asteraceae/chemistry , Esters/chemistry , Esters/isolation & purification , Fatty Acids/analysis , Molecular Conformation , Plant Leaves/chemistry , Plant Stems/chemistry
2.
Z Naturforsch C J Biosci ; 55(1-2): 1-4, 2000.
Article in English | MEDLINE | ID: mdl-10739091

ABSTRACT

A new oxyprenyl coumarin was isolated from the lipophilic exudate of Ozothamnus lycopodioides. Its structure was established as 7-(3,3'-dimethylallyloxy)-5-hydroxy-6-methoxycoumarin from its UV, MS and NMR spectral data, especially two dimensional experiments. In addition to six earlier reported flavonols, we found four highly substituted flavones, including two rare methylenedioxyflavones.


Subject(s)
Asteraceae/chemistry , Coumarins/chemistry , Flavonoids/chemistry , Coumarins/isolation & purification , Flavonoids/isolation & purification , Magnetic Resonance Spectroscopy , Molecular Structure
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