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Hemi-Synthesis and Anti-Oomycete Activity of Analogues of Isocordoin
An efficient synthesis of a series of 4′-oxyalkyl-isocordoin analogues (2–8) is reported for the first time. Their structures were confirmed by (1)H-NMR, (13)C-NMR, and HRMS. Their anti-oomycete activity was evaluated by mycelium and spores inhibition assay against two selected pathogenic oomycetes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152731/ https://www.ncbi.nlm.nih.gov/pubmed/28604594 http://dx.doi.org/10.3390/molecules22060968 |