Synthesis and Fungicidal Activity of 1,3-Thiazoline Derivatives Bearing Nitrophenyl Group on the 2-Position

被引：2
|
作者：
Zhao, Qiuying [1 ,2 ]
Li, Jing [1 ,2 ]
Yan, Xiaojing [1 ,2 ]
Yuan, Huizhu [1 ,2 ]
Qin, Zhaohai [1 ,2 ]
Fu, Bin [1 ,2 ]
机构：
[1] China Agr Univ, Dept Appl Chem, Key Lab Pesticide Chem & Applicat Technol, Beijing 100193, Peoples R China
[2] Chinese Acad Agr Sci, Inst Plant Protect, Beijing 100193, Peoples R China
来源：
JOURNAL OF HETEROCYCLIC CHEMISTRY | 2011年 / 48卷 / 03期
关键词：
LIGANDS; THIAZOLINES; OXAZOLINES; ALKYLATION; CHEMISTRY;
D O I：
10.1002/jhet.570
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Ortho-, meta-, or para-nitro benzoic acid were refluxed with excess SOCl(2) to give acyl chloride, which condensed with beta-amino alcohol in the presence of Et(3)N in dichloromethane to afford beta-hydroxyamide; finally, sulphonation and cyclization were simultaneously conducted to afford 1,3-thiazoline derivatives. Fungicidal activity of these new thiazolines against eight agrocultural fungi were evaluated, and two of this type of compounds displayed good fungicidal activity comparable or superior to commercial fungicide chlorothalonil against two fungi at a concentration of 50 mg/L.
引用
收藏
页码：729 / 732
页数：4
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