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Synthesis and insecticidal activity of O-aryl O-(1,2,2,2-tetrachloroethyl)phosphoramidothioates and their thiophosphoric hydrazides [1]

โœ Scribed by Liang-Nian He; Ming-Wu Ding; Sheng-Biao Li; Qing-Chun Zhou; Yan-Ping Luo; Tian-Jie Wu; Xiao-Peng Liu; Fei Cai


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
136 KB
Volume
10
Category
Article
ISSN
1042-7163

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โœฆ Synopsis


2,

2,

phosphoramidothioates 3a-h and their thiophosphoric hydrazides 4a-e were synthesized by reactions of O-aryl O-(1,2,2,2-tetrachoroethyl)thiophosphorochloridates 2 with amines and hydrazines, respectively. Their structures were characterized by elemental analysis IR 1 H NMR, 31 P NMR, and MS. The O-aryl O-(1,2,2,2tetrachloroethyl)thiophosphoric hydrazides 4a-d (R 2 โ€ซืกโ€ฌH) can be transformed into 1,3,4,2-oxadiazaphospholanes 5a-d by the reaction of triethylamine. The results of preliminary bioassays indicated that some of the title compounds have good insecticidal activities against nematodes (Meloidogyne spp.) and pea aphids.


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