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  • 1
    ISSN: 1573-1561
    Keywords: Pyrus communis cv. Conference ; Rosaceae ; pear ; Psylla pyricola ; leaf sucker ; phenols ; induced plant defense ; 3-O-trans-p-coumaroyltormentic acid ; mass spectrometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The pattern of induction and the chemical structure of phenolic compounds in pear trees (Pyrus communis, cv. Conference) that were either infested by pear leaf suckers Psylla pyricola and P. pyri or mechanically damaged, or both, were studied. Chromatographic (HPLC) and mass spectral analysis performed on extracts of leaf samples collected at various time intervals from trees subjected to three treatments demonstrated the induction (and/or amplification) of a phenolic compound, identified as 3-O-trans-p-coumaroyltormentic acid (I). New mass spectrometric data on this phenolic compound are presented. HPLC revealed different peak patterns in the course of the period of Psylla infestation and the lapse of time since mechanical damage was inflicted, compared to a control tree. The new phenolic compound became apparent after 12 hr and reached the highest level 30 days after damage by pear leaf suckers. It was also observed after 24 hr at lower intensity in samples from a mechanically damaged tree and exclusively on day 30 at very low intensity in the leaf extracts from the uninfested control trees. We conclude that damage by pear leaf suckers, and to a lesser extent also mechanical damage, induce the synthesis of the new, late-eluting phenolic compound. We propose that this compound is involved in plant defense against pear leaf suckers.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1243-1243 
    ISSN: 1434-193X
    Keywords: Correction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Correction
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 692-693 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; Dihydrobenzofuran ; lignans ; 3′,4-O-Dimethylcedrusin ; 4-O-Methylcedrusin ; Dihydrodehydrodiconiferyl alcohol ; Dihydrocarinatinol ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed NMR analysis of 3′,4-O-dimethylcedrusin and 4-O-methylcedrusin using two-dimensional COSY, HETCOR and long-range HETCOR techniques showed that some 13C NMR spectral assignments reported previously for related dihydrobenzofuran lignans such as dihydrodehydrodiconiferyl alcohol and dihydrocarinatinol must be revised.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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