Please use this identifier to cite or link to this item: https://doi.org/10.1021/np990454d
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dc.titleFlavonol-cinnamate cycloadducts and diamide derivatives from Aglaia laxiflora
dc.contributor.authorXu, Y.-J.
dc.contributor.authorWu, X.-H.
dc.contributor.authorTan, B.K.H.
dc.contributor.authorLai, Y.-H.
dc.contributor.authorVittal, J.J.
dc.contributor.authorImiyabir, Z.
dc.contributor.authorMadani, L.
dc.contributor.authorKhozirah, K.S.
dc.contributor.authorGoh, S.H.
dc.date.accessioned2014-06-23T05:39:38Z
dc.date.available2014-06-23T05:39:38Z
dc.date.issued2000-04
dc.identifier.citationXu, Y.-J., Wu, X.-H., Tan, B.K.H., Lai, Y.-H., Vittal, J.J., Imiyabir, Z., Madani, L., Khozirah, K.S., Goh, S.H. (2000-04). Flavonol-cinnamate cycloadducts and diamide derivatives from Aglaia laxiflora. Journal of Natural Products 63 (4) : 473-476. ScholarBank@NUS Repository. https://doi.org/10.1021/np990454d
dc.identifier.issn01633864
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76185
dc.description.abstractLeaf extracts of the Malaysian plant Aglaia laxiflora provided two cytotoxic compounds, a new rocaglaol rhamnoside (1), a known rocaglaol (2), new (but inactive) flavonol-cinnamaminopyrrolidine adducts (36), and their probable biosynthetic precursors (7 and trimethoxyflavonol). All structures were elucidated primarily by 2D NMR spectroscopy. The structure and stereochemistry of aglaxiflorin A (3) were confirmed by single-crystal X-ray crystallography.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/np990454d
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/np990454d
dc.description.sourcetitleJournal of Natural Products
dc.description.volume63
dc.description.issue4
dc.description.page473-476
dc.description.codenJNPRD
dc.identifier.isiut000086820700009
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