Synthesis and Phytotoxic Activity of 1,2,3-Triazole Derivatives

被引:58
|
作者
Borgati, Thiago F. [1 ]
Alves, Rosemeire B. [1 ]
Teixeira, Robson R. [2 ]
de Freitas, Rossimiriam P. [2 ]
Perdigao, Thays G. [2 ]
da Silva, Silma F. [2 ]
dos Santos, Aline Aparecida [2 ]
Bastidas, Alberto de Jesus O. [3 ]
机构
[1] Univ Fed Minas Gerais, Dept Quim, BR-31270900 Belo Horizonte, MG, Brazil
[2] Univ Fed Vicosa, Dept Quim, BR-36570000 Vicosa, MG, Brazil
[3] Nucleo Univ Pedro Rincon Gutierrez, Univ Los Andes, Fac Ciencias, Lab Quim Ecol,Dept Quim, Merida 5101 A, Venezuela
关键词
herbicides; 1,2,3-triazoles; click chemistry; phytotoxicity; HERBICIDES; ALLELOCHEMICALS; DEGRADATION; PRODUCTS;
D O I
10.5935/0103-5053.20130121
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thirteen triazole derivatives bearing halogenated benzyl substituents were synthesized using the Cu-catalyzed azide-alkyne cycloaddition (CuAAC), a leading example of the click chemistry approach, as the key step. The biological activity of the compounds was evaluated, and it was found that these compounds interfere with the germination and radicle growth (shoots and roots) of two dicotyledonous species, Lactuca sativa and Cucumis sativus, and one monocotyledonous species, Allium cepa. The compounds showed predominantly inhibitory activity related to the evaluated species mainly at the concentration of 10(-4) mol L-1. Some of them presented inhibitory activity comparable to 2,4-D (2,4-dichlorophenoxyacetic acid), used as positive control.
引用
收藏
页码:953 / U805
页数:72
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