1980
DOI: 10.1016/0031-9422(80)87030-0
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Neue pyron-derivate aus Helichrysum-arten

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Cited by 50 publications
(26 citation statements)
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“…The presence of ␣-pyrones (12) is rather common (they occur in plants from morphologic groups 1, 2, 4, 12, 15, 18, 19 and 24) and they are often isolated from the roots of these plants (Hänsel et al, 1980;Jakupovic et al, 1986Jakupovic et al, , 1989. Different types of diterpenes occur; these include the kaurenoic acid type (15, Jakupovic et al, 1989) as well as those derived from helifulvanic acid (13, Bohlmann et al, 1980b).…”
Section: Phytochemistrymentioning
confidence: 98%
“…The presence of ␣-pyrones (12) is rather common (they occur in plants from morphologic groups 1, 2, 4, 12, 15, 18, 19 and 24) and they are often isolated from the roots of these plants (Hänsel et al, 1980;Jakupovic et al, 1986Jakupovic et al, , 1989. Different types of diterpenes occur; these include the kaurenoic acid type (15, Jakupovic et al, 1989) as well as those derived from helifulvanic acid (13, Bohlmann et al, 1980b).…”
Section: Phytochemistrymentioning
confidence: 98%
“…dimethoxy- (49,53) and pentamethoxyflavones in DCME (46,47) and methoxy-(51, 52), dimethoxy- (50), and triethoxydimethoxy flavones in ACNE (54,55,57). [22] + + + arenol [23] + + + plicatipyrone analog [22] + arzanol [27] + + + heliarzanol [23] + + cycloarzanol [23] + helipyrone diacetate [25] + + methylarzanol [23] + + 3-[1-[3-acetyl-2,4,6-trihydroxy-5-(3-methyl-2-buten-1-yl)phenyl]ethyl]-6-ethyl-4-hydroxy-5-methyl-2H-pyran-2-one [23] + + auricepyrone [22], 23-methyl-6-O-desmethylauricepyrone [22] + helicerastripyrone [28] [29] + plicatipyrone analog [26]…”
Section: Phytochemical Profilementioning
confidence: 99%
“…Compound Class/Name EE DCME ACNE 2',3'-dihydroxypuberulin [31] + 7-(2,3-dihydroxy-3-methylbutoxy)-5-hydroxy-6-methoxy-2H-1-benzopyran-2-one [32] + + coumarin derivative [33,34] [37] + italipyrone [22] + italipyrone analog [22] + γ-pyrone (chromone) 3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-6-(3-methyl-2-butenyl)-2-phenyl-4H-1-benzopyran-4-one [38] + 2,3-dihydro-5,7-dihydroxy-3-methyl-8-(3-methyl-2-butenyl)-2-(1-methylethyl)-4H-1-benzopyran-4-one [39] + Flavonoid flavone apigenin-7-O-glucoside [4] + apigenin-5-O-glucoside [40] + luteolin [41] + 3,5,6,7,8-pentamethoxyflavone [42] + 3',4',5,6,7-pentamethoxyflavone [43] + apigenin [40] + dihydroxy-dimethoxyflavone [44] + jaceosidin [45] + chrysoeriol [45] + 5,7-dihydroxy-3-methoxyflavone [44] + 5,7,4'-trihydroxy-3,6-dimethoxy-3'-prenylflavone [46] + TEDMF 1 [43] [43] + flavanone naringenin-5-O-glucoside [40] + naringenin-4 -O-glucoside [48] + naringenin-7-O-glucoside [40] + eriodictyol [49] + naringenin [40] + + flavonol quercetin-3-O-glucoside [4], hyperoside (quercetin-3-O-galactoside) [4] + kaempferol-3-O-glucoside [50] + Table 1. Cont.…”
Section: Nomentioning
confidence: 99%
“…These XH and 13C chemical The 13C NMR shifts of C-l' (<5 76.5), C-2' (3 73.2), C-3' (3 74.6), C-5' (3 78.1) and C-6' (3 65. 5) suggested the presence of a polyalcohol moiety. An AB multiplet was observed for 4'-H2 at 3 1.65, 1.80, which showed long range coupling to C-2', C-3', C-5' and C-6' (Fig.…”
Section: Physico-chemical Propertiesmentioning
confidence: 99%