Design, Synthesis, and Biological Activity of Oxime Ether Strobilurin Derivatives Containing Indole Moiety as Novel Fungicide

Twenty‐one novel oxime ether strobilurins containing indole moiety, which employed an indole group to stabilize the E‐styryl group in Enoxastrobin, were designed and synthesized. The biological assay indicated that most compounds exhibited potent fungicidal activities. The structure–activity relatio...

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Veröffentlicht in:	Chemical biology & drug design 2015-06, Vol.85 (6), p.743-755
Hauptverfasser:	Xie, Ya-Qiang, Huang, Zi-Long, Yan, Hui-Dong, Li, Jun, Ye, Li-Yi, Che, Li-Ming, Tu, Song
Format:	Artikel
Sprache:	eng
Schlagworte:	Ethers - chemical synthesis Ethers - chemistry Ethers - pharmacology Fatty Acids, Unsaturated - chemical synthesis Fatty Acids, Unsaturated - chemistry Fatty Acids, Unsaturated - pharmacology Fungi - drug effects fungicidal activities fungicide Fungicides, Industrial - chemical synthesis Fungicides, Industrial - chemistry Fungicides, Industrial - pharmacology indole Indoles - chemical synthesis Indoles - chemistry Indoles - pharmacology Methacrylates - chemical synthesis Methacrylates - chemistry Methacrylates - pharmacology oxime ether Oximes - chemical synthesis Oximes - chemistry Oximes - pharmacology Strobilurins Structure-Activity Relationship
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