The thiazoylmethoxy modifi cation on pyrazole oximes：Synthesis and insecticidal biological evaluation beyond acaricidal activity

注册 English

The thiazoylmethoxy modifi cation on pyrazole oximes：Synthesis and insecticidal biological evaluation beyond acaricidal activity

Hong Dai , Yan-Shuang Xiao , Zhong Li , Xiao-Yong Xu , Xu-Hong Qian

Citation: Hong Dai, Yan-Shuang Xiao, Zhong Li, Xiao-Yong Xu, Xu-Hong Qian. The thiazoylmethoxy modifi cation on pyrazole oximes：Synthesis and insecticidal biological evaluation beyond acaricidal activity[J]. Chinese Chemical Letters, 2014, 25(7): 1014-1016. doi: 10.1016/j.cclet.2014.06.011 shu

shu

The thiazoylmethoxy modifi cation on pyrazole oximes：Synthesis and insecticidal biological evaluation beyond acaricidal activity

通讯作者: Hong Dai,

基金项目:
This workwas financial supported by the National Natural Science Foundation of China (No. 21202089) (No. 21202089)

China Postdoctoral Science Foundation (No. 2013M531145) (No. 2013M531145)

the Research Foundation of the Six People Peak of Jiangsu Province (No. 2013-SWYY-013). (No. 2013-SWYY-013)

摘要: A series of new pyrazole oximes bearing substituted thiazole ring were designed and prepared. The structures of the title compounds were identified by spectral analyses. The results of primary bioassay indicated that some targeted compounds exhibited promising insecticidal activity besides acaricidal activity, particularly; compounds 8c and 8d were more potent against Tetranychus cinnabarinus and Plutella xylostella than other analogues.

关键词:

English

The thiazoylmethoxy modifi cation on pyrazole oximes：Synthesis and insecticidal biological evaluation beyond acaricidal activity

1.
a Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China;
2.
b College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China

Corresponding author: Hong Dai,

Received Date: 15 May 2014
Fund Project:

Abstract: A series of new pyrazole oximes bearing substituted thiazole ring were designed and prepared. The structures of the title compounds were identified by spectral analyses. The results of primary bioassay indicated that some targeted compounds exhibited promising insecticidal activity besides acaricidal activity, particularly; compounds 8c and 8d were more potent against Tetranychus cinnabarinus and Plutella xylostella than other analogues.

Key words:

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