1983
DOI: 10.1007/bf00579957
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Iridoid glycosides ofVerbascum saccatum

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Cited by 5 publications
(12 citation statements)
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“…(see Table I) showed a signal pattern very similar to that of catalpol except for the signals of sugar moieties and those arising from acyl moieties. In addition to four aromatic (b = 7.56 7.67 and 6.36, AX-system, J = 15.8 Hz) arising from the transcinnamoyl moiety, two acetoxy signals were observed at b = Tables I and II) confirmed the identity of 3 as 6-0-ct-L-rhamnopyranosylcatalpol (3,4,5).…”
Section: Resultssupporting
confidence: 66%
“…(see Table I) showed a signal pattern very similar to that of catalpol except for the signals of sugar moieties and those arising from acyl moieties. In addition to four aromatic (b = 7.56 7.67 and 6.36, AX-system, J = 15.8 Hz) arising from the transcinnamoyl moiety, two acetoxy signals were observed at b = Tables I and II) confirmed the identity of 3 as 6-0-ct-L-rhamnopyranosylcatalpol (3,4,5).…”
Section: Resultssupporting
confidence: 66%
“…A combination of polyamide and Si gel column chromatography followed by further purification using reversed-phase chromatography and Sephadex LH 20 column chromatography led to the isolation of several new acylated gmelinosides glycosides A-L (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13) in addition to several known iridoid and phenylpropanoid glycosides. These known compounds were identified by direct comparison with authentic samples and by spectroscopic analysis (UV, IR, 1 H and 13 C NMR, and FABMS) as 6-O-R-L-rhamnopyranosylcatalpol (1), 12 6-O-(3′′-O-trans-feruloyl)-R-L-rhamnopyranosylcatalpol (14), 15 6-O-(2′′-O-acetyl-3′′, 4′′-O-di-trans-cinnamoyl)-R-L-rhamnopyranosylcatalpol (15), 8 verbascoside, 35 and martynoside, 36 respectively.…”
Section: Resultsmentioning
confidence: 98%
“…These known compounds were identified by direct comparison with authentic samples and by spectroscopic analysis (UV, IR, 1 H and 13 C NMR, and FABMS) as 6-O-R-L-rhamnopyranosylcatalpol (1), 12 6-O-(3′′-O-trans-feruloyl)-R-L-rhamnopyranosylcatalpol (14), 15 6-O-(2′′-O-acetyl-3′′, 4′′-O-di-trans-cinnamoyl)-R-L-rhamnopyranosylcatalpol (15), 8 verbascoside, 35 and martynoside, 36 respectively. All 13 C NMR multiplicities of gmelinosides A-L (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13) were confirmed by DEPT measurements, and signal connectivities were determined by HMBC and HMQC. The new iridoid constituents (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13) of G. arborea contained the same iridoid enol-ether system of 6-O-R-L-rhamnopyranosylcatalpol, and were esterified with cinnamoyl or benzoyl derivatives attached to different hydroxyl groups on the sugars or the aglycon moieties.…”
Section: Resultsmentioning
confidence: 99%
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