2020
DOI: 10.3390/molecules25153467
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New Compounds from the Roots of Corsican Calicotome Villosa (Poir.) Link.: Two Pterocarpans and a Dihydrobenzofuran

Abstract: Three new compounds, a dihydrobenzofuran (coumaran) derivative (compound 1) and two pterocarpans (compounds 2 and 3) were isolated from a root extract of Calicotome villosa growing wild in Corsica. Their structures were elucidated using 1D and 2D NMR spectroscopy and MS/MS as 2-(1-methylethenyl)-5-hydroxy-6-carbomethoxy-2,3-dihydro-benzofuran, 4,9-dihydroxy-3-methoxy-2-dimethylallylpterocarpan, and 4,9-dihydroxy-3′,3′-dimethyl-2,3-pyranopterocarpan.

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“…On the other hand, multi signals appeared in the chemical shift range from 6.70 to 7.68 ppm. These correspond to ten protons attributed to the protons of [10,[23][24]. Nickel complex was revealed a good solubility in DMSO solvent at room temperature, while the other complexes were insoluble in all organic solvents so, the 1 H-NMR spectrum data of nickel complex was recorded only in DMSO-d 6 solvent and showed multi signals to aromatic protons at chemical shift δ = 7.63-7.79 ppm.…”
Section: H and 13 C-nmr Spectra Analysismentioning
confidence: 98%
“…On the other hand, multi signals appeared in the chemical shift range from 6.70 to 7.68 ppm. These correspond to ten protons attributed to the protons of [10,[23][24]. Nickel complex was revealed a good solubility in DMSO solvent at room temperature, while the other complexes were insoluble in all organic solvents so, the 1 H-NMR spectrum data of nickel complex was recorded only in DMSO-d 6 solvent and showed multi signals to aromatic protons at chemical shift δ = 7.63-7.79 ppm.…”
Section: H and 13 C-nmr Spectra Analysismentioning
confidence: 98%