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首页> 外文期刊>Pesticide science >Fungitoxicity of hydroxy‐ and methoxy‐substituted phenyl‐ and naphthyl‐benzofurans, phenylbenzobthiophenes and phenylindoles
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Fungitoxicity of hydroxy‐ and methoxy‐substituted phenyl‐ and naphthyl‐benzofurans, phenylbenzobthiophenes and phenylindoles

机译:羟基和甲氧基取代的苯基和萘基苯并呋喃、苯基苯并b噻吩和苯基吲哚的真菌毒性

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AbstractThe antifungal activitiesin vitroof 43 methoxy‐ and hydroxy‐substituted aryl‐benzofurans, phenylbenzobthiophenes and phenylindoles were compared with those of the unsubstituted compounds. Monohydroxy derivatives were usually the most fungitoxic againstAlternaria brassicicola, Botrytis cinerea, Septoria nodorum, Cladosporium cucumerinnum, Fusarium culmorumandUromyces fahaebut the precise effect of substitution upon activity varied with the nature of the parent aryl‐hetocyclic compound, with the position in the molecule, and with the presence of other substituents. Fangitoxicity did not correlate significantly with the partitioning properties of the molecuie as measured by reversed‐phase thin‐layer chr
机译:摘要 比较了43种甲氧基和羟基取代的芳基苯并呋喃、苯并噻吩和苯基吲哚类化合物的体外抗真菌活性。单羟基衍生物通常对链格孢菌、灰霉菌、结节性孢子菌、黄瓜枝孢菌、镰刀菌和法哈乌霉菌的真菌毒性最强,但取代对活性的确切影响因母体芳基-己环化合物的性质、分子中的位置以及其他取代基的存在而异。通过反相薄层 chr 测量的 molecuie 的分配特性没有显着相关性

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