Synthesis of strigolactones analogues by intramolecular [2+2] cycloaddition of ketene-iminium salts to olefins and their activity on Orobanche cumana seeds

Strigolactones have been the latest identified phytohormones. Among the strigolactones analogues described recently, GR-24 remains the most studied derivative which is used as standard in this field. In order to improve several properties of GR-24 for potential agronomical applications, we investiga...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2014-05, Vol.24 (9), p.2123-2128
Hauptverfasser: Lachia, Mathilde, Wolf, Hanno Christian, De Mesmaeker, Alain
Format: Artikel
Sprache:eng
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Zusammenfassung:Strigolactones have been the latest identified phytohormones. Among the strigolactones analogues described recently, GR-24 remains the most studied derivative which is used as standard in this field. In order to improve several properties of GR-24 for potential agronomical applications, we investigated the effect of substituents on the B and C-rings on the activity for seed germination induction. We report here the synthesis of 9 GR-24 analogues via a [2+2] intramolecular cycloaddition of ketene-iminium salts and a summary of their activity for the germination of Orobanche cumana (broomrape) seeds.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2014.03.044