%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 (3−6), 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