%0 Journal Article %A Xu, Yuan-Jian %A Wu, Xiao-Hua %A Tan, B. K. H. %A Lai, Yee-Hing %A Vittal, J. J. %A Imiyabir, Z. %A Madani, L. %A Khozirah, K. S. %A Goh, S. H. %D 2000 %T Flavonol−Cinnamate Cycloadducts and Diamide Derivatives from Aglaia laxiflora %U https://acs.figshare.com/articles/journal_contribution/Flavonol_Cinnamate_Cycloadducts_and_Diamide_Derivatives_from_i_Aglaia_laxiflora_i_/3734973 %R 10.1021/np990454d.s001 %2 https://ndownloader.figshare.com/files/5826741 %K adduct %K biosynthetic precursors %K trimethoxyflavonol %K crystallography %K Cycloadduct %K 2 D NMR spectroscopy %K stereochemistry %K Malaysian plant Aglaia laxiflora %K Flavonol %K cytotoxic compounds %K Diamide Derivatives %K flavonol %K aglaxiflorin %K rocaglaol rhamnoside %K Aglaia laxiflora Leaf extracts %X Leaf 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. %I ACS Publications