10.1021/np990454d.s001
Yuan-Jian Xu
Yuan-Jian
Xu
Xiao-Hua Wu
Xiao-Hua
Wu
B. K. H. Tan
B. K. H.
Tan
Yee-Hing Lai
Yee-Hing
Lai
J. J. Vittal
J. J.
Vittal
Z. Imiyabir
Z.
Imiyabir
L. Madani
L.
Madani
K. S. Khozirah
K. S.
Khozirah
S. H. Goh
S. H.
Goh
Flavonol−Cinnamate Cycloadducts and Diamide Derivatives from <i>Aglaia
laxiflora</i>
American Chemical Society
2000
adduct
biosynthetic precursors
trimethoxyflavonol
crystallography
Cycloadduct
2 D NMR spectroscopy
stereochemistry
Malaysian plant Aglaia laxiflora
Flavonol
cytotoxic compounds
Diamide Derivatives
flavonol
aglaxiflorin
rocaglaol rhamnoside
Aglaia laxiflora Leaf extracts
2000-03-22 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/Flavonol_Cinnamate_Cycloadducts_and_Diamide_Derivatives_from_i_Aglaia_laxiflora_i_/3734973
Leaf extracts of the Malaysian plant <i>Aglaia laxiflora </i>provided two cytotoxic compounds, a new rocaglaol
rhamnoside (<b>1</b>), a known rocaglaol (<b>2</b>), new (but inactive) flavonol−cinnamaminopyrrolidine adducts (<b>3</b>−<b>6</b>), and their probable biosynthetic precursors (<b>7</b> and trimethoxyflavonol). All structures were elucidated
primarily by 2D NMR spectroscopy. The structure and stereochemistry of aglaxiflorin A (<b>3</b>) were confirmed
by single-crystal X-ray crystallography.