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1.
Molecules ; 14(2): 598-607, 2009 Feb 04.
Article in English | MEDLINE | ID: mdl-19214150

ABSTRACT

Friedelin (1), 3beta-friedelinol (2), 28-hydroxyfriedelin (3), 16alpha-hydroxyfriedelin (4), 30-hydroxyfriedelin (5) and 16alpha,28-dihydroxyfriedelin (6) were isolated through fractionation of the hexane extract obtained from branches of Salacia elliptica. After a week in CDCl(3) solution, 16alpha-hydroxyfriedelin (4) reacted turning into 3-oxo-16-methylfriedel-16-ene (7). This is the first report of a dehydration followed by a Nametkin rearrangement of a pentacyclic triterpene in CDCl(3) solution occurring in the NMR tube. These seven pentacyclic triterpenes was identified through NMR spectroscopy and the stereochemistry of compound 4 and 7 was established by 2D NMR (NOESY) spectroscopy and mass spectrometry (GC-MS). It is also the first time that all the (13)C-NMR and 2D NMR spectral data are reported for compounds 4 and 7.


Subject(s)
Magnetic Resonance Spectroscopy , Triterpenes/chemistry , Drugs, Chinese Herbal/chemistry , Magnetic Resonance Spectroscopy/methods , Molecular Conformation , Molecular Structure , Salacia/chemistry , Stereoisomerism
2.
Magn Reson Chem ; 45(10): 895-8, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17729233

ABSTRACT

The compounds 3-oxofriedelane (1), 3beta-hydroxyfriedelane (2), 3,11-dioxofriedelane (3), 3,16-dioxofrie delane (4) and 3-oxo-12alpha-hydroxyfriedelane (5) were isolated from the hexane extract of Maytenus gonoclada Mart. (Celastraceae) leaves. Structural formula and the stereochemistry of the new pentacyclic triterpene 3-oxo-12alpha-hydroxyfriedelane (5) were established through (1)H and (13)C NMR and DEPT 135 spectral data including 2D experiments (HMBC, HMQC, COSY, and NOESY) and mass spectrometry (GC-MS).


Subject(s)
Magnetic Resonance Spectroscopy/methods , Maytenus/chemistry , Triterpenes/chemistry , Carbohydrate Sequence , Carbon Isotopes , Nitrogen Isotopes
3.
J Chromatogr B Analyt Technol Biomed Life Sci ; 828(1-2): 103-7, 2005 Dec 15.
Article in English | MEDLINE | ID: mdl-16221575

ABSTRACT

A headspace solid phase microextraction (SPME) method has been developed to determine metabolites of dimethylformamide, N-hydroxymethyl-N-methylformamide, and N-methylformamide (NMF) as NMF in urine by gas chromatography with nitrogen-phosphorus detector (GC-NPD). An SPME holder with a 65-microm PDMS/DVB fiber coating was used. Optimal desorption conditions were 250 degrees C for 1 min, adsorption at 80 degrees C for 15 min, and 3.00 mL of sample in the headspace vial. The method presented good resolution, repeatability, recovery, detection limit, ruggedness and response linearity.


Subject(s)
Chromatography, Gas/methods , Dimethylformamide/analogs & derivatives , Formamides/analysis , Urine/chemistry , Dimethylformamide/analysis , Humans , Reproducibility of Results
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