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N-Azolyl Phenoxypyrimidine Herbicides: Novel Inhibitors of Carotenoid Biosynthesis Part 1

机译:N-乙氧基苯氧基嘧啶除草剂:类胡萝卜素生物合成部分的新型抑制剂

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Substituted 2-azolyl-4-phenoxypyrimidines of formula 1 represent a new family of highly active herbicides that act by inhibiting carotenoid biosynthesis. Azole substituents on the pyrimidine are nitrogen-linked and include pyrazole, imidazole and triazole. These compounds are active preemergence and postemergence but tend to be more active preemergence. Selectivity was observed on wheat, corn, and soybeans. There was particular interest in these compounds as cereal herbicides for preemergent and early-postemergent weed control. High field efficacy was observed, particularly on broadleaf weeds. Pyrazolylpyrimidine 1a showed optimum activity in cereal field trials and gave excellent broadleaf weed control at rates as low at 5-10 g/ha, with good wheat safety. This paper will focus on chemistry, biology, structure-activity relationships, mode-of-action, and field activity for compounds of this herbicide class.
机译:式1的取代的2-唑烯基-4-苯氧基吡啶胺代表了通过抑制类胡萝卜素生物合成来作用的高活性除草剂的新系列。嘧啶上的唑代取代基是氮气连接的,包括吡唑,咪唑和三唑。这些化合物是活跃的促进和后期的,但往往是更活跃的备注。在小麦,玉米和大豆上观察到选择性。对于谷物除草剂,这些化合物特别兴趣,用于射精和早期后干杂草对照。观察到高场疗效,特别是在阔叶杂草上。吡唑吡啶胺1A在谷物场试验中显示出最佳活性,并以5-10g / ha为低于5-10克/公顷的速率优异的阔叶杂草控制,具有良好的小麦安全性。本文将专注于该除草剂类化合物的化学,生物学,结构 - 活性关系,动作模式和田间活性。

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