1985
DOI: 10.1016/0016-7037(85)90072-9
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Tetracyclic diterpenoid hydrocarbons in some Australian coals, sediments and crude oils

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Cited by 271 publications
(64 citation statements)
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“…The presence of diterpenoid compounds in these samples is evidence of the influence of higher plant debris, particularly of conifers, in the formation of the sediments (Noble et al, 1985;Venkatesan et al, 1986). In the peat we observed a predominance of diterpenoid adds whereas the lignite contained a predominance of defunctionalized and aromatized diterpenes, suggesting its higher maturity.…”
Section: Diterpenoid Compoundsmentioning
confidence: 55%
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“…The presence of diterpenoid compounds in these samples is evidence of the influence of higher plant debris, particularly of conifers, in the formation of the sediments (Noble et al, 1985;Venkatesan et al, 1986). In the peat we observed a predominance of diterpenoid adds whereas the lignite contained a predominance of defunctionalized and aromatized diterpenes, suggesting its higher maturity.…”
Section: Diterpenoid Compoundsmentioning
confidence: 55%
“…The greater abundance of these compounds in the lignite samples suggests a larger contribution from resinous higher plants in the lignite than in the According to those authors, the great abundance of these compounds and the absence of their saturated analogs implies that the precursor plant material has been rapidly buried and preserved from oxidation and biodegradation and, consequently, diagenetic reduction of the diterpenes has been limited. A saturated compound was identified by its mass spectrum (base peak at m/z 123 and molecular ion at m/z 274) as 16¢(H)-phyllocladane (VIH), the isomer most commonly found in some other fignites (Serantoni et al, 1978;Noble et al, 1985;Alexander et al, 1987). Kaurenes and phyllocladenes (unsaturated diterpenes) are typical components of conifer resins belonging to Podocarpaceae, Araucariaceae and Cupressaceae families (Hanson, 1968;Thomas, 1969).…”
Section: Diterpenoid Compoundsmentioning
confidence: 99%
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“…They are identified according to the spectra published by Noble et al (1985). Their spectra are all characterized by a molecular ion at m/z 274 and a base peak at m/z 123 (C 20 H 34 ).…”
Section: Tetracyclic Diterpenoids Mainly Ent-beyerane 16α(h)-and 16mentioning
confidence: 99%
“…Diterpenoids, which are regarded as specific compounds of conifers (e.g., Noble et al, 1985;Chaffee et al, 1986) Dinosterane/4-desmethylsterane ratio, the ratio of the compound specific to dinoflag ellatesto that widely occurring in algae, is rela tivelyhigher in the bottom part of the Onna gawaFormation and the Tentokuji Formation than in the middle and upper parts of the On nagawaFormation and the Funakawa Forma tion (Fig. 4), indicating a decrease of the con tributionof dinoflagellates at ca.…”
Section: Introductionmentioning
confidence: 99%