2017
DOI: 10.6023/cjoc201611029
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Synthesis and Herbicidal Activity of Novel Cyanoacrylates Containing Substituted Pyridyl Moiety

Abstract: In order to find new cyanoacrylate lead compounds, a series of novel cyanoacrylates containing substituted pyridyl moiety were prepared by the method of active substructure combination. The structures of the target compounds were confirmed by 1 H NMR, 13 C NMR and elemental analyses. Preliminary bioassay data displayed that in postemergence treatment 2-cyano-3-methylthio-3-[4-(5-trifluoromethylpyridyl-2-amino)]benzylamino(2-methoxy)ethyl ester (7l) had 95% herbicidal activity against Brassica juncea at 1500 g/… Show more

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Cited by 3 publications
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“…Intermediates 1 – 3 were synthesized with reported procedures [ 31 ]. Intermediates 6 – 8 were prepared according to the literature method [ 32 ].…”
Section: Methodsmentioning
confidence: 99%
“…Intermediates 1 – 3 were synthesized with reported procedures [ 31 ]. Intermediates 6 – 8 were prepared according to the literature method [ 32 ].…”
Section: Methodsmentioning
confidence: 99%
“…Dai (Nantong University) in collaboration with Shi (Jiangsu University of Science and Technology and later Nantong University) also focused their attention on (substituted)­benzylamino-2-cyanoacrylates (general structure XXI in Figure ). When R 1 is methoxyethyl or ethoxyethyl, 3-methylthio-2-cyanoacrylates with a (4,6-dimethoxypyrimidin-2-yl)­thio group or 5-(trifluoromethyl)­pyridin-2-amino group , at the para position of benzylamino exhibited good herbicidal activity against Brassica juncea, Stellaria media, and Chenopodium serotinum L. at a dosage of 1500 g ha –1 , while when R 1 is changed to another substituted phenoxyethyl group, the activity decreased sharply.…”
Section: Herbicidal 2-cyanoacrylatesmentioning
confidence: 99%