Synthesis of both enantiomers of altholactone, isoaltholactone and 5-hydroxygoniothalamin from tri-O-acetyl-D-glucal, and their biological activities

Citation
A. Hiratate et al., Synthesis of both enantiomers of altholactone, isoaltholactone and 5-hydroxygoniothalamin from tri-O-acetyl-D-glucal, and their biological activities, J PESTIC S, 26(4), 2001, pp. 366-370
Citations number
10
Categorie Soggetti
Entomology/Pest Control
Journal title
JOURNAL OF PESTICIDE SCIENCE
ISSN journal
03851559 → ACNP
Volume
26
Issue
4
Year of publication
2001
Pages
366 - 370
Database
ISI
SICI code
0385-1559(2001)26:4<366:SOBEOA>2.0.ZU;2-5
Abstract
Both enantiomers of altholactone, isoaltholactone and 5-hydroxygoniothalami n were synthesized from tri-O-acetyl-D-glucal. and biological activities of altholactones were examined, For brine shrimp. the configuration or 3-hydr oxy group at convex site was important for lethal activity. while (2S,3S)-c onfiguration was inhibitory to lettuce germination.