2014
DOI: 10.5935/0103-5053.20140127
|View full text |Cite
|
Sign up to set email alerts
|

New Phenolic Glycosides fromPhyllanthus cochinchinensis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 0 publications
0
2
0
Order By: Relevance
“…The relative configuration of glucose anomeric proton was confirmed as β on the basis of the coupling constant ( J 1′, 2′  = 7.8 Hz). Furthermore, the glucose was identified as D-form by GC analysis comparing with a standard after acid hydrolysis [12, 13]. The relative configuration of 1 was same with mascaroside I by comparison of the NMR data.…”
Section: Resultsmentioning
confidence: 99%
“…The relative configuration of glucose anomeric proton was confirmed as β on the basis of the coupling constant ( J 1′, 2′  = 7.8 Hz). Furthermore, the glucose was identified as D-form by GC analysis comparing with a standard after acid hydrolysis [12, 13]. The relative configuration of 1 was same with mascaroside I by comparison of the NMR data.…”
Section: Resultsmentioning
confidence: 99%
“…As reported in the previous literature, 14 compound 1(3 mg) was hydrolyzed with 2 mol L −1 HCl–dioxane (1:1, v/v, 5 mL) at 85°C for 8 h. The reaction mixture was extracted with CHCl 3 (2 mL × 4). The aqueous layer was neutralized with 2 mol L −1 NaOH and dried to obtain the monosaccharides.…”
Section: Hydrolysis Of Compound 1 and Gc Analysismentioning
confidence: 99%