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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and Herbicidal Activity of O,O-Dialkyl N-[2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yloxy)benzoxyl]-1-a mino-1-substitutedbenzyl Phosphonates
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Synthesis and Herbicidal Activity of O,O-Dialkyl N-[2-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yloxy)benzoxyl]-1-a mino-1-substitutedbenzyl Phosphonates

机译:O,O-二烷基N- [2-(5,7-二甲基-[1,2,4]三唑并[1,5-a]嘧啶-2-基氧基)苯甲酰基] -1-a氨基的合成及除草活性-1-取代的苯基膦酸酯

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摘要

A series of novel 1.2,4-triazolo[1,5-a]pyrimidine derivatives containing an a-amino phosphonate moiety 5 were designed and synthesized by the multi-step reactions. Their structures were clearly confirmed by spectroscopic data (IR, H-1 NMR, P-31 NMR, MS) and elemental analysis, compound 5b was further determined by X-ray diffraction crystallography. The results of preliminary bioassay indicated that some of the title compounds 5 possessed moderate herbicidal activities against dicotyledonous plants (Brassica campestris L) at the concentration of 100 mg/L. For example, compound 5i possessed 92.0% inhibitory activity against B. campestris L and showed better activity than that of the commercialized herbicide Bispyribac-sodium; however, compounds 5 displayed weak herbicidal activity at the concentration of 10 mg/L.
机译:通过多步反应设计并合成了一系列含有α-氨基膦酸酯部分5的新型1.2,4-三唑并[1,5-a]嘧啶衍生物。通过光谱数据(IR,H-1 NMR,P-31 NMR,MS)和元素分析清楚地确认了它们的结构,进一步通过X射线衍射晶体学确定了化合物5b。初步生物测定的结果表明,某些标题化合物5在100 mg / L的浓度下对双子叶植物(Brassica campestris L)具有中等的除草活性。例如,化合物5i对野菜双歧杆菌L具有92.0%的抑制活性,并显示出比商品化除草剂双嘧贝酸钠的更好的活性。但是,化合物5在10 mg / L的浓度下除草活性较弱。

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