<abstract xmlns="http://www.w3.org/1999/xhtml">

Chromatographic separation of methanolic extract of <italic>Baphia nitida</italic> heartwood gave two crystalline solids characterized as 3,9-dimethoxy-6aR,11aR-dihydro-6H-benzofuro(3,2-C)[1]benzopyran (also known as homopterocarpin) with molecular formula C17H16O4 (1.57% yield) and 2,4-dimethoxybenzaldehyde C9H10O3 (2.27% yield). Each of the isolated compounds showed a single spot on developed thin layer chromatographic plate under ultra-violet light (254 nm) and spray reagent (10% sulfuric acid in methanol solution). Structural elucidation was achieved using Fourier transform infrared (FT-IR) spectroscopy, one and two-dimension nuclear magnetic resonance (NMR) techniques. Distortionless enhancement by polarization transfer-edited-heteronuclear single quantum coherence (DEPT-ed-HSQC) was also a useful tool that aided the characterization of the two secondary metabolites isolated from <italic>Baphia nitida</italic> heartwood.
</abstract>

Chromatographic separation of methanolic extract of Baphia nitida heartwood gave two crystalline solids characterized as 3,9-dimethoxy-6aR,11aR-dihydro-6H-benzofuro(3,2-C)[1]benzopyran (also known as homopterocarpin) with molecular formula C17H16O4 (1.57% yield) and 2,4-dimethoxybenzaldehyde C9H10O3 (2.27% yield). Each of the isolated compounds showed a single spot on developed thin layer chromatographic plate under ultra-violet light (254 nm) and spray reagent (10% sulfuric acid in methanol solution). Structural elucidation was achieved using Fourier transform infrared (FT-IR) spectroscopy, one and two-dimension nuclear magnetic resonance (NMR) techniques. Distortionless enhancement by polarization transfer-edited-heteronuclear single quantum coherence (DEPT-ed-HSQC) was also a useful tool that aided the characterization of the two secondary metabolites isolated from Baphia nitida heartwood.

Isolation of an isoflavonoid and a terpenoid from the heartwood of <italic>Baphia nitida</italic> Lodd. (camwood)

Ovidius University Annals of Chemistry

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Isolation of an isoflavonoid and a terpenoid from the heartwood of  Lodd. (camwood)

Chromatographic separation of methanolic extract of Baphia nitida heartwood gave two crystalline solids characterized as...

Isolation of an isoflavonoid and a terpenoid from the heartwood of Baphia nitida Lodd. (camwood)

Publié en ligne: 03 mars 2020

Pages: 5 - 8

Reçu: 26 oct. 2019

Accepté: 23 févr. 2020

DOI: https://doi.org/10.2478/auoc-2020-0002

Mots clés
camwood, isolation, chromatography, secondary metabolites, homopterocarpin, isoflavonoid, terpenoid

© 2020 Gloria Ihuoma Ndukwe et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Isolation of an isoflavonoid and a terpenoid from the heartwood of Baphia nitida Lodd. (camwood)

Publié en ligne: 03 mars 2020

Pages: 5 - 8

Reçu: 26 oct. 2019

Accepté: 23 févr. 2020

DOI: https://doi.org/10.2478/auoc-2020-0002

Mots cléscamwood, isolation, chromatography, secondary metabolites, homopterocarpin, isoflavonoid, terpenoid

© 2020 Gloria Ihuoma Ndukwe et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Mots clés
camwood, isolation, chromatography, secondary metabolites, homopterocarpin, isoflavonoid, terpenoid