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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...
Tallennettuna:
| Julkaisussa: | Molecules |
|---|---|
| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6152731/ https://ncbi.nlm.nih.gov/pubmed/28604594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules22060968 |
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