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Synthesis and Fungicidal Activities of Aryl Thiocarbamic Acid-5-aryl-2-furanmethyl Ester
Li Yang1,3; Li Baoju2; Yang Xinling1; Shi Yanxia2; Miao Hongjian1; Ling Yun1
刊名CHINESE JOURNAL OF ORGANIC CHEMISTRY
2011
卷号31期号:9页码:1411-1418
关键词benzoylureas chitin aryl thiocarbamic acid-5-aryl-2-furanmethyl ester fungicidal activity
ISSN号0253-2786
通讯作者Li Yang
英文摘要To find new pesticide lead compounds with high activity and low toxicity, chitin was chosen as the research target. 23 novel aryl thiocarbamic acid-5-aryl-2-furanmethyl esters were designed and synthesized from substituted benzoic acid and 5-aryl-2-furanmethanol. Their structures were confirmed by IR, (1)H NMR and elemental analysis. The preliminary bioassay results indicated that some compounds showed obvious inhibition effects against Corynespora cassiicola, Botrytis cinereapers, Fusarium oxysporum, especially to Botrytis cinereapers in which most compounds showed higher inhibitory rate than control fungicide 40% WP dimethachlon.
学科主题Chemistry, Organic ; CHEMISTRY, ORGANIC
语种中文
出版者SCIENCE PRESS
WOS记录号WOS:000295758400009
内容类型期刊论文
源URL[http://111.203.20.206/handle/2HMLN22E/101139]  
专题蔬菜花卉研究所_植物保护研究室
作者单位1.China Agr Univ, Key Lab Pesticide Chem & Applicat, Minist Agr, Dept Appl Chem,Coll Sci, Beijing 100193, Peoples R China
2.Chinese Acad Agr Sci, Inst Vegetables & Flowers, Beijing 100081, Peoples R China
3.Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China
推荐引用方式
GB/T 7714
Li Yang,Li Baoju,Yang Xinling,et al. Synthesis and Fungicidal Activities of Aryl Thiocarbamic Acid-5-aryl-2-furanmethyl Ester[J]. CHINESE JOURNAL OF ORGANIC CHEMISTRY,2011,31(9):1411-1418.
APA Li Yang,Li Baoju,Yang Xinling,Shi Yanxia,Miao Hongjian,&Ling Yun.(2011).Synthesis and Fungicidal Activities of Aryl Thiocarbamic Acid-5-aryl-2-furanmethyl Ester.CHINESE JOURNAL OF ORGANIC CHEMISTRY,31(9),1411-1418.
MLA Li Yang,et al."Synthesis and Fungicidal Activities of Aryl Thiocarbamic Acid-5-aryl-2-furanmethyl Ester".CHINESE JOURNAL OF ORGANIC CHEMISTRY 31.9(2011):1411-1418.
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