{"title":"一种异黄酮和萜类化合物的分离纯化。(紫木)","authors":"G. Ndukwe, A. Oluah, G. K. Fekarurhobo","doi":"10.2478/auoc-2020-0002","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":19641,"journal":{"name":"Ovidius University Annals of Chemistry","volume":"28 1","pages":"5 - 8"},"PeriodicalIF":1.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"Isolation of an isoflavonoid and a terpenoid from the heartwood of Baphia nitida Lodd. (camwood)\",\"authors\":\"G. Ndukwe, A. Oluah, G. K. Fekarurhobo\",\"doi\":\"10.2478/auoc-2020-0002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":19641,\"journal\":{\"name\":\"Ovidius University Annals of Chemistry\",\"volume\":\"28 1\",\"pages\":\"5 - 8\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ovidius University Annals of Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2478/auoc-2020-0002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ovidius University Annals of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/auoc-2020-0002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Isolation of an isoflavonoid and a terpenoid from the heartwood of Baphia nitida Lodd. (camwood)
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.