PHEROMONE SYNTHESIS, CXCI - SYNTHESIS OF THE ENANTIOMERS OF 8-HYDROXY-2,5,8-TRIMETHYL-4-NONANONE, THE MYXOBACTERIAL PHEROMONE OF STIGMATELLA-AURANTIACA TO INDUCE THE FORMATION OF ITS FRUITING BODY

Authors
Citation
K. Mori et M. Takenaka, PHEROMONE SYNTHESIS, CXCI - SYNTHESIS OF THE ENANTIOMERS OF 8-HYDROXY-2,5,8-TRIMETHYL-4-NONANONE, THE MYXOBACTERIAL PHEROMONE OF STIGMATELLA-AURANTIACA TO INDUCE THE FORMATION OF ITS FRUITING BODY, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, (10), 1998, pp. 2181-2184
Citations number
4
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
1434193X
Issue
10
Year of publication
1998
Pages
2181 - 2184
Database
ISI
SICI code
1434-193X(1998):10<2181:PSC-SO>2.0.ZU;2-2
Abstract
The enantiomers of the title compound 1 were synthesized from the enan tiomers of citronellol (2). Both (R)- and (S)-1 induced the formation of the fruiting body of a myxo-bacterium Stigmatella aurantiaca at a c oncentration of 0.4-1.0 nM.