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Synthesis, Crystal Structure and Biological Activities of O, O-Dialkyl α-[1-(2-Chlorothiazol-5-ylmethyl)-5-methyl- 1 H-1,2,3-triazol-4-ylcarbonyloxy]alkylphosphonates
引用本文:陈小保,石德清,朱小飞.Synthesis, Crystal Structure and Biological Activities of O, O-Dialkyl α-[1-(2-Chlorothiazol-5-ylmethyl)-5-methyl- 1 H-1,2,3-triazol-4-ylcarbonyloxy]alkylphosphonates[J].中国化学,2007,25(12):1854-1858.
作者姓名:陈小保  石德清  朱小飞
作者单位:Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei 430079, China
基金项目:Project supported by the National Natural Science Foundation of China (No. 20302002).
摘    要:In order to search for novel agrochemicals with high activity and low toxicity, a series of phosphonate derivatives containing 1,2,3-triazole and thiazole rings were designed and synthesized using 2-chloro-5-(chloromethyl)- thiazole as the starting material. Their structures were confirmed by IR, ^1H NMR, ^31p NMR, EI-MS or ESI-MS and elemental analyses. The crystal structure of 7a was determined by single crystal X-ray diffraction. Preliminary bioassays indicated that most of the target compounds did not display insecticidal activities, but a fraction of them possessed herbicidal and fungicidal activities to some extent.

关 键 词:噻唑  1  2  3-三唑  氢氧化物  生物活性
收稿时间:2007-03-11
修稿时间:2007-06-01

Synthesis,Crystal Structure and Biological Activities of O,O‐Dialkyl α‐[1‐(2‐Chlorothiazol‐5‐ylmethyl)‐5‐methyl‐ 1H‐1,2,3‐triazol‐4‐ylcarbonyloxy]alkylphosphonates
CHEN, Xiao-Bao SHI, De-Qing ZHU, Xiao-Fei.Synthesis,Crystal Structure and Biological Activities of O,O‐Dialkyl α‐[1‐(2‐Chlorothiazol‐5‐ylmethyl)‐5‐methyl‐ 1H‐1,2,3‐triazol‐4‐ylcarbonyloxy]alkylphosphonates[J].Chinese Journal of Chemistry,2007,25(12):1854-1858.
Authors:CHEN  Xiao-Bao SHI  De-Qing ZHU  Xiao-Fei
Institution:Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei 430079, China
Abstract:In order to search for novel agrochemicals with high activity and low toxicity, a series of phosphonate derivatives containing 1,2,3‐triazole and thiazole rings were designed and synthesized using 2‐chloro‐5‐(chloromethyl)‐ thiazole as the starting material. Their structures were confirmed by IR, 1H NMR, 31P NMR, EI‐MS or ESI‐MS and elemental analyses. The crystal structure of 7a was determined by single crystal X‐ray diffraction. Preliminary bioassays indicated that most of the target compounds did not display insecticidal activities, but a fraction of them possessed herbicidal and fungicidal activities to some extent.
Keywords:thiazole  1  2  3‐triazole  α‐hydroxyalkylphosphonate  biological activity
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