1998
DOI: 10.1002/(sici)1099-0690(199806)1998:6<1205::aid-ejoc1205>3.0.co;2-k
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Cameroonane, Prenopsane and Nopsane, Three New Tricyclic Sesquiterpene Skeletons

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Cited by 58 publications
(65 citation statements)
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“…Two new lignans together with the known lupeol and sitosteryl ß-D-glucopyranoside, have been isolated from the roots of E. giganteus var. lelyi C. D. Adams Compositae) (Tene et al, 2004); Sesquiterpenoids have been previously isolated from the essential oil (Menut et al, 1997;Weyerstahl et al, 1998). However, there are no previous reports on the antituberculosis activity and chemical nature of the antituberculosis compounds in E. giganteus.…”
Section: Resultsmentioning
confidence: 99%
“…Two new lignans together with the known lupeol and sitosteryl ß-D-glucopyranoside, have been isolated from the roots of E. giganteus var. lelyi C. D. Adams Compositae) (Tene et al, 2004); Sesquiterpenoids have been previously isolated from the essential oil (Menut et al, 1997;Weyerstahl et al, 1998). However, there are no previous reports on the antituberculosis activity and chemical nature of the antituberculosis compounds in E. giganteus.…”
Section: Resultsmentioning
confidence: 99%
“…[1,13] Tricyclic alcohol 1 and β-caryophyllene ( 14 ) (Figure 4) were also isolated from the same natural sources in numerous reports. [9,14] These findings suggested that three classes of polycyclic sesquiterpenes were connected in a common biosynthetic pathway. In 1980, Bohlmann explained these results by proposing that farnesyl pyrophosphate (FPP) ( 21 ) undergoes enzymatic polycyclization to caryophyllenyl cation 23 (Scheme 1A).…”
Section: The Presilphiperfolanol Natural Productsmentioning
confidence: 96%
“…Presilphiperfol-7(8)-ene ( 6 ) [9] presumably arises from the deprotonation of presilphiperfolanyl cation intermediates. Natural products such as the britanlins ( 7 – 9 ) [10] display additional oxidation at primary carbons in the presilphiperfolane skeleton.…”
Section: The Presilphiperfolanol Natural Productsmentioning
confidence: 99%
“…112,118 We discovered that this ratio can be improved in favor of the natural compound (±)-69 using diisobutylaluminum hydride at low temperatures. 120,123 Thus, products (±)-69 and (±)-epi-69 were obtained in a ratio of 3.7:1.…”
Section: (±)-Cameroonanolmentioning
confidence: 99%