A lot of insecticides are found nowadays, but neonicotinoids are considered the most famous. So, a series of pyridine derivatives neonicotinoids analogues, namely, 3-cyano-4,6-dimethylpyridine-2(1)-one (), 2-chloro-3-cyano-4,6-dimethylpyridine (), 3-cyano-4,6-dimethylpyridine-2(1)-thione (), 3-cyano-4,6-distyrylpyridine-2(1)-thione (), 2-((3-cyano-4,6-distyrylpyridin-2-yl)thio)--phenylacetamide (), 3-amino--phenyl-4,6-distyrylthieno[2,3-]pyridine-2-carboxamide (), 2-((3-cyano-4,6-distyrylpyridin-2-yl)thio)--(-tolyl)acetamide (), 3-amino-4,6-distyryl--(-tolyl)thieno[2,3-]pyridine-2-carboxamide (), 2-((3-cyano-4,6-distyrylpyridin-2-yl)thio)--(4-methoxyphenyl)acetamide (), and 3-amino--(4-methoxyphenyl)-4,6-distyrylthieno[2,3-]pyridine-2-carboxamide (), have been designed and synthesized in pure state, and their agricultural bioefficacy as insecticides against cowpea aphid Koch was screened. The structures of the synthesized compounds were verified by means of spectroscopic and elemental analyses.
View Article and Find Full Text PDFNeonicotinoids are the most widely used from all existing pesticides. So, in purpose to discover new pesticides being more effective against the aphid, twelve heterocyclic compounds neonicotinoid analogs have been prepared in a pure state; pyrimidothienotetrahydroisoquinolines and their toxicity as potential insecticidal agents against cowpea Aphid, Koch was screened. Their characterizations by using spectroscopic analyses were performed.
View Article and Find Full Text PDFNeonicotinoids are the most important class of insecticides used in agriculture over the last decade. They act as selective agonists of insect nicotinic acetylcholine receptors (nAChRs). The emergence of insect resistance to these insecticides is one of the major problems, which limit the use of neonicotinoids.
View Article and Find Full Text PDFInsect vector-borne diseases remain one of the principal causes of human mortality. In addition to conventional measures of insect control, repellents continue to be the mainstay for personal protection. Because of the increasing pyrethroid-resistant mosquito populations, alternative strategies to reconstitute pyrethroid repellency and knock-down effects have been proposed by mixing the repellent DEET (N,N-Diethyl-3-methylbenzamide) with non-pyrethroid insecticide to better control resistant insect vector-borne diseases.
View Article and Find Full Text PDFFive pyridine derivatives, namely, N-morpholinium 7,7-dimethyl-3-cyano-4-(4'-nitrophenyl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-2-thiolate (1), sodium 5-acetyl-3-amino-4-(4'-methoxyphenyl)-6-methylthieno[2,3-b] pyridine-2-carboxylate (2), piperidinium 3,5-dicyano-2-oxo-4-spirocyclopentane-1,2,3,4-tetrahydropyridine-6-thiolate (3), piperidinium 5-acetyl-3-cyano-4-(4'-methoxyphenyl)-6-methylpyridine-2-thiolate (4), and piperidinium 5-acetyl-4-(4'-chlorophenyl)-3-cyano-6-methyl-pyridine-2-thiolate (5) were prepared in pure state and subjected to the title study. The bioassay results indicated that the insecticidal activity of compound 1 is about 4-fold that of acetamiprid insecticide. The rest of the tested compounds possess moderate to strong aphidicidal activities.
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