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RELATION BETWEEN STRUCTURE AND HERBICIDAL ACTIVITY OF SUBSTITUTED BENZONITRILES

 

作者: H. KOOPMAN,   J. DAAMS,  

 

期刊: Weed Research  (WILEY Available online 1965)
卷期: Volume 5, issue 4  

页码: 319-326

 

ISSN:0043-1737

 

年代: 1965

 

DOI:10.1111/j.1365-3180.1965.tb00359.x

 

出版商: Blackwell Publishing Ltd

 

数据来源: WILEY

 

摘要:

Summary.The herbicidal activity of substituted benzonitriles was determined by a number of tests. This activity was compared with the structure of the molecules. It was found experimentally that benzonitriles, substituted at the 2 and 6 positions by halogen or methyl, had the highest activity. Some 2,6‐dichloro‐1‐substituted benzene derivatives showed a herbicidal activity, comparable with that of 2,6‐dichlorobenzonilrile. These compounds possessed a group which could be converted into a nitrilc group.La relation entre la structure ft l'activité herbicide des benzonitril‐es

 

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