Synthesis of both enantiomers of altholactone, isoaltholactone and 5-hydroxygoniothalamin from tri-O-acetyl-D-glucal, and their biological activities
2001
Hiratate, A. (Tohoku Univ., Sendai (Japan)) | Kiyota, H. | Noshita, T. | Takeuchi, R. | Oritani, T.
Both enantiomers of altholactone, isoaltholactone and 5-hydroxygoniothalamin were synthesized from tri-0-acetyl-D-glucal, and biological activities of altholactones were examined. For brine shrimp, the configuration of 3-hydroxy group at convex site was important for lethal activity, while (2S, 3S) - configuration was inhibitory to lettuce germination.
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Библиографическая информация
Нумерация страниц
pp. 366-370
Язык
Английский
Примечание
Summaries (En, Ja)
1 table; 1 fig.; 10 ref.
Тип
Summary
2005-05-15
AGRIS AP
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