2006
DOI: 10.1016/j.bse.2006.01.010
|View full text |Cite
|
Sign up to set email alerts
|

Phenylpropanoid glycerols from Tillandsia streptocarpa Baker (Bromeliaceae)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
10
0

Year Published

2007
2007
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(10 citation statements)
references
References 27 publications
0
10
0
Order By: Relevance
“…The natural occurrence of hydroxycinnamoyldiglycerides in plants seems to be restricted to a small number of species among the Poaceae, Liliaceae, Sparganiaceae and Bromeliaceae [55]. In particular, representatives of these species are adapted to hot and/or arid climates and habitats such as sorghum (Sorghum bicolor (L.) Moench), Tillandsia spp.…”
Section: Phenolic Pattern Of Different Fruit Tissuesmentioning
confidence: 99%
“…The natural occurrence of hydroxycinnamoyldiglycerides in plants seems to be restricted to a small number of species among the Poaceae, Liliaceae, Sparganiaceae and Bromeliaceae [55]. In particular, representatives of these species are adapted to hot and/or arid climates and habitats such as sorghum (Sorghum bicolor (L.) Moench), Tillandsia spp.…”
Section: Phenolic Pattern Of Different Fruit Tissuesmentioning
confidence: 99%
“…Therefore, SA4 was identified to be an glycerol ester with two acid units, one being caffeic acid and the other p‐coumaric acid. In comparison of the data with the literature value (Cooper, Gottlieb, & Lavie, ; Delaporte, Guzen, Laverde, Santos, & Sarragiotto, ), the compound SA4 was concluded to be 1‐O‐p‐coumaroyl‐3‐O‐caffeoylglycerol (Figure b).…”
Section: Resultsmentioning
confidence: 60%
“…Its IR spectrum indicated the presence of hydroxyl (3023 cm -1 ), ester carbonyl (1683 cm -1 ) and aromatic rings (1601 and 1512 cm -1 ). Analysis of the 1 H and 13 C NMR spectrum (Table II) of compound 2 suggested its structure is closely related to that of 1-O-feruloyl-3-O-p-coumaroylglycerol (Delaporte et al, 2006), except that the 7' and 8' protons of the feruloyl moiety had different chemical shifts and coupling constant. In the 1 H NMR spectrum of 2, one pair of signals for olefinic protons appeared at δ H 5.82 and 6.86 (each 1H, d, J = 12.8 Hz).…”
Section: Resultsmentioning
confidence: 99%
“…Up to now, natural phenylpropanoid glycerols have been reported from species of Gramineae (Cooper et al, 1978;Koshino et al, 1988), Liliaceae (Shimomura et al, 1987;Shimomura et al, 1988;Mimaki et al, 1989;Jang et al, 2004), Sparganiaceae (Shirota et al, 1996), Juncaceae (Dellagreca et al, 1998), Bromeliaceae (Queiroga et al, 2004;Delaporte et al, 2006).…”
Section: Resultsmentioning
confidence: 99%