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作为植物源除草剂的薄荷烷 -7-胺衍生物的设计、合成及除草活性

Design, synthesis, and herbicidal activity of -menthane-7-amine derivatives as botanical herbicides.

作者信息

Zhang Hongmei, Chen Yuxiang, Xu Shichao, Wang Jing, Dong Huanhuan, Zhao Zhendong, Jiang Jianxin

机构信息

Institute of Chemical Industry of Forest Products, CAF, National Engineering Lab. for Biomass Chemical Utilization, Key Lab. of Biomass Energy and Material, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Key Lab. of Chemical Engineering of Forest Products, National Forestry and Grassland Administration No. 16 Suojin Wucun Jiangsu Province Nanjing 210042 China

College of Materials Science and Technology, Beijing Forestry University No. 35 Qinghua Dong Lu Beijing 100083 China

出版信息

RSC Adv. 2021 Aug 9;11(44):27207-27214. doi: 10.1039/d1ra04910k.

Abstract

In this study, a series of novel -menthane type secondary amines (-menthane-7-amine derivatives 3a-3y) were synthesized and then characterized by FTIR, H NMR, C NMR, and HRMS. The post-emergence herbicidal activities of these amines against barnyard grass and rape were evaluated by the culture dish method. Most of the -menthane-7-amine derivatives showed excellent herbicidal activities equivalent to or even higher than either diuron or glyphosate. The alkyl-substituted derivatives were more active than the phenyl-substituted derivatives. The herbicidal activities of compounds 3p, 3r, 3u, and 3w against the root growth of barnyard grass were 404% higher, respectively, than those of glyphosate. The herbicidal activities of compounds 3q, 3v, 3w, and 3x against the root growth of rape were 561%, 494%, 491%, and 544% higher, respectively, than those of diuron, and 484%, 760%, 423%, and 665% higher respectively, than those of diuron against shoot growth of rape. In addition, compounds 3p, 3u, and 3v are almost harmless to rice, wheat, sorghum, maize, and peanuts at a concentration of 100 mg L. Most of the compounds are nontoxic to HUVEC-C and BALB/c 3T3 cells. It is indicated that the title compounds could be utilized as botanical herbicides for future weed control.

摘要

在本研究中,合成了一系列新型薄荷烷型仲胺(薄荷烷-7-胺衍生物3a - 3y),然后通过傅里叶变换红外光谱(FTIR)、氢核磁共振(¹H NMR)、碳核磁共振(¹³C NMR)和高分辨质谱(HRMS)对其进行了表征。采用培养皿法评估了这些胺对稗草和油菜的苗后除草活性。大多数薄荷烷-7-胺衍生物表现出优异的除草活性,等同于甚至高于敌草隆或草甘膦。烷基取代衍生物比苯基取代衍生物更具活性。化合物3p、3r、3u和3w对稗草根生长的除草活性分别比草甘膦高404%。化合物3q、3v、3w和3x对油菜根生长的除草活性分别比敌草隆高561%、494%、491%和544%,对油菜地上部分生长的除草活性分别比敌草隆高484%、760%、423%和665%。此外,化合物3p、3u和3v在浓度为100 mg/L时对水稻、小麦、高粱、玉米和花生几乎无害。大多数化合物对人脐静脉内皮细胞(HUVEC-C)和BALB/c 3T3细胞无毒。结果表明,标题化合物可作为未来杂草防治的植物源除草剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4460/9037671/5f095a739a8e/d1ra04910k-s1.jpg

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