1977
DOI: 10.1016/0040-4020(77)80444-4
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Novel hydroxy lignans from the heartwood of gmelina arborea

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Cited by 67 publications
(25 citation statements)
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“…Eight amides, two lignans and four other compounds were isolated from the hexane and methanol extracts of Piper sarmentosum fruits and identified by spectroscopic methods: pellitorine (1) (Likhitwitayawuid et al, 1987), guineensine (2) (Okogun and Ekong, 1974;Koul et al, 1988), brachystamide B (3) (Banerji and Das, 1989), sarmentine (4) (Likhitwitayawuid et al, 1987), brachyamide B (5) (Koul et al, 1988), 1-piperettyl pyrrolidine (6) (Singh et al, 1974), 3 ,4 ,5 -trimethoxycinnamoyl pyrrolidine (7) (Achenbach et al, 1986), sarmentosine (8) (Likhitwitayawuid et al, 1987), (+)-asarinin (9) (Pelter et al, 1976), sesamin (10) (Pelter et al, 1976;Anjaneyulu et al, 1977), 1-(3,4-methylenedioxyphenyl)-1E-tetradecene (11) (Likhitwitayawuid et al, 1987), methyl piperate (12) (Kijjoa et al, 1989) and a mixture of ␤-sitosterol (13) (Pouchert and Behnke, 1993) and stigmasterol (14) (Pouchert and Behnke, 1993). The structures of compounds 1-14 are presented in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Eight amides, two lignans and four other compounds were isolated from the hexane and methanol extracts of Piper sarmentosum fruits and identified by spectroscopic methods: pellitorine (1) (Likhitwitayawuid et al, 1987), guineensine (2) (Okogun and Ekong, 1974;Koul et al, 1988), brachystamide B (3) (Banerji and Das, 1989), sarmentine (4) (Likhitwitayawuid et al, 1987), brachyamide B (5) (Koul et al, 1988), 1-piperettyl pyrrolidine (6) (Singh et al, 1974), 3 ,4 ,5 -trimethoxycinnamoyl pyrrolidine (7) (Achenbach et al, 1986), sarmentosine (8) (Likhitwitayawuid et al, 1987), (+)-asarinin (9) (Pelter et al, 1976), sesamin (10) (Pelter et al, 1976;Anjaneyulu et al, 1977), 1-(3,4-methylenedioxyphenyl)-1E-tetradecene (11) (Likhitwitayawuid et al, 1987), methyl piperate (12) (Kijjoa et al, 1989) and a mixture of ␤-sitosterol (13) (Pouchert and Behnke, 1993) and stigmasterol (14) (Pouchert and Behnke, 1993). The structures of compounds 1-14 are presented in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…(Table 32). 13C chemical shifts for steroids (577)(578)(579) and four epimers of 20,22-epoxycholesterol (580a-580c) are listed in Table 33. Epoxides (580 a-580 d), which were synthesized and their 13C spectra recorded, exhibit characteristic chemical shifts, permitting unambiguous assignment of sidechain stereochemistry (152,153).…”
Section: Referencespp195-229mentioning
confidence: 99%
“…In this study, we isolated eleven lignans (1±11) from the CH 2 Cl 2 fraction of the bark of M. thunbergii. The lignans were identi®ed as (À)-acuminatin (1) (El-Feraly et al 1982), (À)-isoguaiacin (2) (King & Wilson 1964), meso-dihydroguaiaretic acid (3) (Shimomura et al 1988), ( )-galbacin (4) (Achenbach et al 1987;Hada et al 1988), (À)sesamin (5) (Ajaneyulu et al 1977), ( )-galbelgin (6) (Holloway & Scheinmann 1974), machilin A (7) (Shimomura et al 1987), machilin G (8) (Shimomura et al 1988), licarin A (9) (Achenbach et al 1987), nectandrin A (10) (Shimomura et al 1988) and B (11) (Shimomura et al 1988). Among the lignans described, (À)-acuminatin and (À)-isoguaiacin are reported as components of Lauraceae for the ®rst time.…”
mentioning
confidence: 99%