Acetogenic isoquinoline alkaloids.: Part 127 -: Cis- and trans-isoshinanolone from Dioncophyllum thollonii:: absolute configuration of two 'known', wide-spread natural products

被引:27
作者
Bringmann, G
Münchbach, M
Messer, K
Koppler, D
Michel, M
Schupp, O
Wenzel, M
Louis, AM
机构
[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[2] Herbier Natl Gabon, Libreville, Gabon
关键词
Dioncophyllum thollonii; Dioncophyllaceae; cis-isoshinanolone; trans-isoshinanolone; tetralones; naturally occurring; ruthenium-mediated oxidative degradation; structural elucidation; stereochemistry;
D O I
10.1016/S0031-9422(99)00080-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
From the rare West African liana, Dioncophyllum thollonii (Dioncophyllaceae), the known acetogenic tetralones, cis- and trans-isoshinanolone, were isolated. Exemplarily on this material, a new ruthenium-catalyzed oxidative degradation procedure, related to the well-established stereoanalysis of 1,3-dimethyltetrahydroisoquinolines lines, was ela berated. The method allo ws to unambiguously attribute the absolute configuration of these natural products, which likewise occur in several other plant species. For the rapid discrimination between the four possible stereoisomeric forms of isoshinanolone (i.e. the cis- and transdiastereomers and their enantiomers), an HPLC-analytical procedure on a chiral stationary phase has been developed. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:693 / 699
页数:7
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