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  • 1
    ISSN: 1432-2048
    Keywords: Fruit set and growth ; Gibberellin (distribution in fruit, fruit growth, quantitation, transport) ; Parthenocarpy ; Pisum (fruit growth)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In addition to the previously-reported gibberellins: GA1; GA8, GA20 and GA29 (García-Martínez et al., 1987, Planta 170, 130–137), GA3 and GA19 were identified by combined gas chromatography-mass spectrometry in pods and ovules of 4-d-old pollinated pea (Pisum sativum cv. Alaska) ovaries. Pods contained additionally GA17, GA81 (2α-hydroxy GA20) and GA29-catabolite. The concentrations of GA1, GA3, GA8, GA19, GA20 and GA29 were higher in the ovules than in the pod, although, with the exception of GA3, the total content of these GAs in the pod exceeded that in the seeds. About 80% of the GA3 content of the ovary was present in the seeds. The concentrations of GA19 and GA20 in pollinated ovaries remained fairly constant for the first 12 ds after an thesis, after which they increased sharply. In contrast, GA1 and GA3 concentrations were maximal at 7 d and 4–6 d, respectively, after anthesis, at about the time of maximum pod growth rate, and declined thereafter. Emasculated ovaries at anthesis contained GA8, GA19 and GA20 at concentrations comparable with pollinated fruit, but they decreased rapidly. Gibberellins a1 and A3 were present in only trace amounts in emasculated ovaries at any stage. Parthenocarpic fruit, produced by decapitating plants immediately above an emasculated flower, or by treating such flowers with 2,4-dichlorophenoxyacetic acid or GA7, contained GA19 and GA20 at similar concentrations to seeded fruit, but very low amounts of GA1 and GA3 Thus, it appears that the presence of fertilised ovules is necessary for the synthesis of these last two GAs. Mature leaves and leaf diffusates contained GA1, GA8, GA19 and GA20 as determined by combined gas chromatography-mass spectrometry using selected ion monitoring. This provides further evidence that vegetative tissues are a possible alternative source of GAs for fruit-set, particularly in decapitated plants.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 311-314 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Substituent chemical shift values ; π bond orders ; Methoxy-substituted aromatic compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The substituent chemical shift values induced by the methoxy group at the two ortho positions of aromatic compounds which include naphthalenes, quinolines, indoles, coumarins, flavones and benzofurans were linearly correlated with π-bond orders, affording the equation Δδortho(13C) = -98.68Pπ + 50.38 (correlation coefficient = 0.929; root mean square error = 1.95 ppm) when 40 pairs of values are considered. Elimination of six points corresponding to ring-junction quaternary carbons improves the correlation coefficient to 0.961 (root mean square error = 1.4 ppm) for the equation Δδortho(13C) = -126.85Pπ + 69.66.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 299-304 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Quipazines Substituted quinolines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complete assignment of the 13C NMR spectra of a series of biologically active quipazines substituted at position C-5, C-6 or C-7 of the quinoline moiety provides evidence for a strong conjugation between the π-electron cloud of the pyridine ring and the nitrogen lone pair of the piperazinyl residue. The SCS values of these quipazines are compared with those of the analogous quinolines, and their deviations are discussed in terms of conjugation effects.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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