Direct Qualitative and Quantitative Analysis of Triterpenes Using 13C NMR Spectroscopy Exemplified by Dichloromethanic Extracts of Cork

1999 ◽  
Vol 53 (3) ◽  
pp. 344-350 ◽  
Author(s):  
Vincent Castola ◽  
Ange Bighelli ◽  
Joseph Casanova
2014 ◽  
Vol 79 (11) ◽  
pp. 1355-1362 ◽  
Author(s):  
Vele Tesevic ◽  
Ivana Aljancic ◽  
Slobodan Milosavljevic ◽  
Vlatka Vajs ◽  
Iris Djordjevic ◽  
...  

The aerial parts of three endemic Centaurea L. species, namely C. tomorosii Micevski, C. soskae Hayek and C. galicicae Micevski, afforded sesquiterpene lactone cnicin (1) and seven flavonoids: apigenin (2), isokaempferide (3), hispidulin (4), eupatorin (5), cirsimaritin (6), santaflavone (7) and salvigenin (8). The structures of the isolated compounds were determined by UV, 1H NMR and 13C NMR spectroscopy and HR-ESI-MS spectrometry. 1H NMR spectroscopy was used as a method for quantitative analysis of sesquiterpene lactone cnicin.


2015 ◽  
Vol 7 (12) ◽  
pp. 5226-5238 ◽  
Author(s):  
Photis Dais ◽  
Maria Misiak ◽  
Emmanuel Hatzakis

The objective of this study is the qualitative and quantitative analysis of encapsulated fish oil supplements by utilizing high-resolution multinuclear (1H,13C,31P) and multidimensional NMR spectroscopy.


2007 ◽  
Vol 40 (2) ◽  
pp. 936
Author(s):  
D. Papoulis

The application of 27Al and 29Si CPMAS NMR spectroscopy to the investigation of selected /caolinite and dickite bearing samples from hydrothermally altered rhyolites of Kos island is tested using also XRD and analytical SEM-EDS data. Kaolinite and dickite, can be detected by both their tetrahedral Si and octahedral Al CPMAS NMR spectra. It was found that the interference of the peaks become less significant and the shape of the peaL· narrow when the pulse recycling delay is high (up to 10s). The octahedral Al / tetrahedral Si ratios of kaolinite group mineral forms from samples showing various degrees of alteration, calculated from the NMR spectra, were found to be very similar to these derived from the structural formulae of SEM-EDS microanalyses. In this work it is presented for the first time an approach to provide narrow CPMAS NMR peaks. The narrow shape of the peaks provides accurate measurements of the exact position of the peaL· and the octahedral Al / tetrahedral Si ratios.


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