articleTop 10% cited
Isolation and NMR Spectral Studies of Dihydromyricetin
Journal of Pharmacognosy and Phytochemistry · 2013 · Vol. 2(4) · pp. 113–115
Abstract
From the alcoholic extract of the leaves of Hovenia dulcis, a pentahydroxyl flavanonol has been isolated as a major compound, whose structure has been characterized as dihydromyricetin (DHM) on the basis of extensive 1D and 2D Nuclear Magnetic Resonance (NMR) as well as High Resolution Mass Spectral (HRMS) data. Also, a comparative study of the 1H and 13C NMR spectral data of dihydromyricetin has been studied in three different solvent systems namely C5D5N (d5-pyridine) or CD3OD (d4-methanol) or C2D6SO (d6-DMSO).
Medicinal plant effects and applicationsBiological Activity of Diterpenoids and BiflavonoidsNatural product bioactivities and synthesisMethanolChemistryTwo-dimensional nuclear magnetic resonance spectroscopyCarbon-13 NMRPyridineSolventSpectral analysisNuclear magnetic resonanceProton NMRNuclear magnetic resonance spectroscopy
Citations
13
FWCI
4.52
field-weighted impact
References
8
Percentile
94%
vs. same field & year
Citations per year
Citation Network
How this paper connects to the literature. Drag to explore, click any node to open that paper.