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Cycloalkyl substituted N-nitrourea derivatives: a convenient synthesis and biological evaluation

机译:环烷基取代的N-硝基脲衍生物:方便的合成和生物学评估

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摘要

A series of N-nitrourea derivatives bearing various cycloalkyl were conveniently obtained via three steps including nitration, carbamic chlorination, and aminolysis reactions. The structures of all newly synthesized compounds were elucidated and confirmed by IR, (1)H NMR, (13)C NMR, and elemental analysis. The preliminary bioassay indicated that the target compounds exhibited moderate herbicidal activity against Amaranthus albus and Sorghum sudanense. However, some of the title compounds presented high plant growth regulating activity against rice.
机译:通过包括硝化,氨基甲酸氯化和氨基分解反应的三个步骤,可以方便地获得一系列带有各种环烷基的N-硝基脲衍生物。通过IR,(1)H NMR,(13)C NMR和元素分析阐明并确认了所有新合成的化合物的结构。初步的生物测定表明,目标化合物对白mar和苏丹草具有中等的除草活性。但是,一些标题化合物对水稻具有很高的植物生长调节活性。

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