1987
DOI: 10.1007/bf00602483
|View full text |Cite
|
Sign up to set email alerts
|

Iridoid glycosides ofVerbascum sinuatum

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
11
0

Year Published

1990
1990
2022
2022

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(11 citation statements)
references
References 2 publications
0
11
0
Order By: Relevance
“…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%
See 4 more Smart Citations
“…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%
See 3 more Smart Citations