An efficient synthesis of a series of 4-oxyalkyl-isocordoin analogues (2–8) is reported for the first time. Their structures were confirmed by1H-NMR,13C-NMR, and HRMS. Their anti-oomycete activity was evaluated by mycelium and spores inhibition assay against two selected pathogenic oomycetes stra...
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http://repositorio.unab.cl/xmlui/handle/ria/4747
Escobar, B.
,
Montenegro, I.
,
Villena, J.
,
Werner, E.
,
Godoy, P.
,
Olguín, Y.
,
Madrid, A.
,
[Hemi-Synthesis and Anti-Oomycete Activity of Analogues of Isocordoin]
,
Hemi-Synthesis and Anti-Oomycete Activity of Analogues of Isocordoin
